[{"versioned_ensembl_gene_id":"ENSG00000283891.1","gene_symbol":"MIR628","gene_name":"microRNA 628 [Source:HGNC Symbol;Acc:HGNC:32884]","synonyms":"MIRN628,hsa-mir-628","biotype":"miRNA","ncbi_id":"693213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55372940,"end":55373034,"strand":-1,"description":"microRNA 628 [Source:HGNC Symbol;Acc:HGNC:32884]"}, {"versioned_ensembl_gene_id":"ENSG00000251931.1","gene_symbol":"RNU6-871P","gene_name":"RNA, U6 small nuclear 871, pseudogene [Source:HGNC Symbol;Acc:HGNC:47834]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479950","summary":null,"start":59450673,"end":59450772,"strand":-1,"description":"RNA, U6 small nuclear 871, pseudogene [Source:HGNC Symbol;Acc:HGNC:47834]"}, {"versioned_ensembl_gene_id":"ENSG00000207766.1","gene_symbol":"MIR626","gene_name":"microRNA 626 [Source:HGNC Symbol;Acc:HGNC:32882]","synonyms":"MIRN626,hsa-mir-626","biotype":"miRNA","ncbi_id":"693211","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41691585,"end":41691678,"strand":1,"description":"microRNA 626 [Source:HGNC Symbol;Acc:HGNC:32882]"}, {"versioned_ensembl_gene_id":"ENSG00000275323.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000276678.1","gene_symbol":"GHRLOS","gene_name":"Ghrelin opposite strand RNA conserved region [Source:RFAM;Acc:RF02126]","synonyms":"NCRNA00068,GHRL-AS1","biotype":"misc_RNA","ncbi_id":"100126793","summary":"This gene is an antisense gene of the ghrelin/obestatin prepropeptide gene. Alternatively spliced transcript variants have been identified and they may function as non-coding regulatory RNAs. [provided by RefSeq, Jan 2013]","start":10287413,"end":10287482,"strand":1,"description":"Ghrelin opposite strand RNA conserved region [Source:RFAM;Acc:RF02126]"}, {"versioned_ensembl_gene_id":"ENSG00000207260.1","gene_symbol":"RNU6-35P","gene_name":"RNA, U6 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:34279]","synonyms":"RNU6-35","biotype":"snRNA","ncbi_id":"100873750","summary":null,"start":109992325,"end":109992431,"strand":1,"description":"RNA, U6 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:34279]"}, {"versioned_ensembl_gene_id":"ENSG00000265993.1","gene_symbol":"MIR5694","gene_name":"microRNA 5694 [Source:HGNC Symbol;Acc:HGNC:43530]","synonyms":"hsa-mir-5694","biotype":"miRNA","ncbi_id":"100847064","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67441855,"end":67441930,"strand":-1,"description":"microRNA 5694 [Source:HGNC Symbol;Acc:HGNC:43530]"}, {"versioned_ensembl_gene_id":"ENSG00000207185.1","gene_symbol":"RNU6-1157P","gene_name":"RNA, U6 small nuclear 1157, pseudogene [Source:HGNC Symbol;Acc:HGNC:48120]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481545","summary":null,"start":118593988,"end":118594093,"strand":1,"description":"RNA, U6 small nuclear 1157, pseudogene [Source:HGNC Symbol;Acc:HGNC:48120]"}, {"versioned_ensembl_gene_id":"ENSG00000283793.1","gene_symbol":"MIR6861","gene_name":"microRNA 6861 [Source:HGNC Symbol;Acc:HGNC:50129]","synonyms":"hsa-mir-6861","biotype":"miRNA","ncbi_id":"102465519","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112163258,"end":112163321,"strand":-1,"description":"microRNA 6861 [Source:HGNC Symbol;Acc:HGNC:50129]"}, {"versioned_ensembl_gene_id":"ENSG00000201545.1","gene_symbol":"RNU4-85P","gene_name":"RNA, U4 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47021]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479597","summary":null,"start":19996803,"end":19996925,"strand":1,"description":"RNA, U4 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47021]"}, {"versioned_ensembl_gene_id":"ENSG00000272439.1","gene_symbol":"RNU6-91P","gene_name":"RNA, U6 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47054]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479606","summary":null,"start":99444306,"end":99444412,"strand":1,"description":"RNA, U6 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47054]"}, {"versioned_ensembl_gene_id":"ENSG00000241821.3","gene_symbol":"RN7SL170P","gene_name":"RNA, 7SL, cytoplasmic 170, pseudogene [Source:HGNC Symbol;Acc:HGNC:46186]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479283","summary":null,"start":56688401,"end":56688695,"strand":1,"description":"RNA, 7SL, cytoplasmic 170, pseudogene [Source:HGNC Symbol;Acc:HGNC:46186]"}, {"versioned_ensembl_gene_id":"ENSG00000265889.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36285312,"end":36285413,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207194.1","gene_symbol":"RNU6-1026P","gene_name":"RNA, U6 small nuclear 1026, pseudogene [Source:HGNC Symbol;Acc:HGNC:47989]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480631","summary":null,"start":50582404,"end":50582511,"strand":1,"description":"RNA, U6 small nuclear 1026, pseudogene [Source:HGNC Symbol;Acc:HGNC:47989]"}, {"versioned_ensembl_gene_id":"ENSG00000283621.1","gene_symbol":"MIR6759","gene_name":"microRNA 6759 [Source:HGNC Symbol;Acc:HGNC:50063]","synonyms":"hsa-mir-6759","biotype":"miRNA","ncbi_id":"102466729","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57748618,"end":57748682,"strand":-1,"description":"microRNA 6759 [Source:HGNC Symbol;Acc:HGNC:50063]"}, {"versioned_ensembl_gene_id":"ENSG00000264032.1","gene_symbol":"MIR4491","gene_name":"microRNA 4491 [Source:HGNC Symbol;Acc:HGNC:41808]","synonyms":"hsa-mir-4491","biotype":"miRNA","ncbi_id":"100616330","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111347757,"end":111347824,"strand":1,"description":"microRNA 4491 [Source:HGNC Symbol;Acc:HGNC:41808]"}, {"versioned_ensembl_gene_id":"ENSG00000207172.1","gene_symbol":"RNU6-1162P","gene_name":"RNA, U6 small nuclear 1162, pseudogene [Source:HGNC Symbol;Acc:HGNC:48125]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480078","summary":null,"start":63630678,"end":63630781,"strand":1,"description":"RNA, U6 small nuclear 1162, pseudogene [Source:HGNC Symbol;Acc:HGNC:48125]"}, {"versioned_ensembl_gene_id":"ENSG00000206629.1","gene_symbol":"RNU1-63P","gene_name":"RNA, U1 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:48405]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480664","summary":null,"start":67429591,"end":67429754,"strand":-1,"description":"RNA, U1 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:48405]"}, {"versioned_ensembl_gene_id":"ENSG00000283558.1","gene_symbol":"hsa-mir-3158-1","gene_name":"hsa-mir-3158-1 [Source:miRBase;Acc:MI0014186]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":101601417,"end":101601497,"strand":-1,"description":"hsa-mir-3158-1 [Source:miRBase;Acc:MI0014186]"}, {"versioned_ensembl_gene_id":"ENSG00000252735.1","gene_symbol":"RNU6-528P","gene_name":"RNA, U6 small nuclear 528, pseudogene [Source:HGNC Symbol;Acc:HGNC:47491]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479800","summary":null,"start":33338867,"end":33338966,"strand":1,"description":"RNA, U6 small nuclear 528, pseudogene [Source:HGNC Symbol;Acc:HGNC:47491]"}, {"versioned_ensembl_gene_id":"ENSG00000252319.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8720034,"end":8720132,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201912.1","gene_symbol":"RN7SKP189","gene_name":"RNA, 7SK small nuclear pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:45913]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479180","summary":null,"start":145057108,"end":145057437,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:45913]"}, {"versioned_ensembl_gene_id":"ENSG00000274122.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28387160,"end":28387417,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200162.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153607377,"end":153607479,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200163.1","gene_symbol":"SNORD115-18","gene_name":"small nucleolar RNA, C/D box 115-18 [Source:HGNC Symbol;Acc:HGNC:33037]","synonyms":"HBII-52-18","biotype":"snoRNA","ncbi_id":"100033456","summary":null,"start":25203227,"end":25203308,"strand":1,"description":"small nucleolar RNA, C/D box 115-18 [Source:HGNC Symbol;Acc:HGNC:33037]"}, {"versioned_ensembl_gene_id":"ENSG00000276764.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18958147,"end":18958413,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275994.1","gene_symbol":"SNORA24","gene_name":"small nucleolar RNA, H/ACA box 24 [Source:HGNC Symbol;Acc:HGNC:32614]","synonyms":"SNORA24A,ACA24","biotype":"snoRNA","ncbi_id":"677809","summary":null,"start":118279190,"end":118279320,"strand":1,"description":"small nucleolar RNA, H/ACA box 24 [Source:HGNC Symbol;Acc:HGNC:32614]"}, {"versioned_ensembl_gene_id":"ENSG00000277950.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20070716,"end":20070965,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222308.1","gene_symbol":"RNA5SP198","gene_name":"RNA, 5S ribosomal pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:43098]","synonyms":"RN5S198","biotype":"rRNA","ncbi_id":"100873460","summary":null,"start":151875566,"end":151875692,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:43098]"}, {"versioned_ensembl_gene_id":"ENSG00000201965.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38125292,"end":38125394,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252264.1","gene_symbol":"RNU7-153P","gene_name":"RNA, U7 small nuclear 153 pseudogene [Source:HGNC Symbol;Acc:HGNC:45687]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479082","summary":null,"start":14319455,"end":14319516,"strand":1,"description":"RNA, U7 small nuclear 153 pseudogene [Source:HGNC Symbol;Acc:HGNC:45687]"}, {"versioned_ensembl_gene_id":"ENSG00000200121.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":175176493,"end":175176586,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251770.1","gene_symbol":"RNA5SP486","gene_name":"RNA, 5S ribosomal pseudogene 486 [Source:HGNC Symbol;Acc:HGNC:43386]","synonyms":"RN5S486","biotype":"rRNA","ncbi_id":"100873728","summary":null,"start":47873191,"end":47873273,"strand":1,"description":"RNA, 5S ribosomal pseudogene 486 [Source:HGNC Symbol;Acc:HGNC:43386]"}, {"versioned_ensembl_gene_id":"ENSG00000202217.1","gene_symbol":"RN7SKP47","gene_name":"RNA, 7SK small nuclear pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45771]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481974","summary":null,"start":74799895,"end":74800222,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45771]"}, {"versioned_ensembl_gene_id":"ENSG00000244748.3","gene_symbol":"RN7SL153P","gene_name":"RNA, 7SL, cytoplasmic 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:46169]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480490","summary":null,"start":72314397,"end":72314688,"strand":-1,"description":"RNA, 7SL, cytoplasmic 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:46169]"}, {"versioned_ensembl_gene_id":"ENSG00000251972.1","gene_symbol":"RNU6-123P","gene_name":"RNA, U6 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:47086]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479620","summary":null,"start":25943044,"end":25943145,"strand":-1,"description":"RNA, U6 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:47086]"}, {"versioned_ensembl_gene_id":"ENSG00000212607.1","gene_symbol":"SNORA3B","gene_name":"small nucleolar RNA, H/ACA box 3B [Source:HGNC Symbol;Acc:HGNC:32638]","synonyms":"ACA3-2,SNORA45B,SNORA45","biotype":"snoRNA","ncbi_id":"677826","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA45, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":8685439,"end":8685569,"strand":1,"description":"small nucleolar RNA, H/ACA box 3B [Source:HGNC Symbol;Acc:HGNC:32638]"}, {"versioned_ensembl_gene_id":"ENSG00000283290.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":24352057,"end":24352157,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207321.1","gene_symbol":"RNU6-160P","gene_name":"RNA, U6 small nuclear 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:47123]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479637","summary":null,"start":153331622,"end":153331728,"strand":1,"description":"RNA, U6 small nuclear 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:47123]"}, {"versioned_ensembl_gene_id":"ENSG00000273541.1","gene_symbol":"DLEU1_2","gene_name":"Deleted in lymphocytic leukemia 1 conserved region 2 [Source:RFAM;Acc:RF02104]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50104833,"end":50105174,"strand":1,"description":"Deleted in lymphocytic leukemia 1 conserved region 2 [Source:RFAM;Acc:RF02104]"}, {"versioned_ensembl_gene_id":"ENSG00000253792.1","gene_symbol":"AC025437.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158173601,"end":158176422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284185.1","gene_symbol":"MIR219A2","gene_name":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]","synonyms":"MIRN219-2,MIR219-2,hsa-mir-219-2,MIRN219-2,MIR219-2,hsa-mir-219-2","biotype":"miRNA","ncbi_id":"407003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128392618,"end":128392714,"strand":-1,"description":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]"}, {"versioned_ensembl_gene_id":"ENSG00000263858.1","gene_symbol":"MIR4769","gene_name":"microRNA 4769 [Source:HGNC Symbol;Acc:HGNC:41694]","synonyms":"hsa-mir-4769","biotype":"miRNA","ncbi_id":"100616147","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47587429,"end":47587505,"strand":1,"description":"microRNA 4769 [Source:HGNC Symbol;Acc:HGNC:41694]"}, {"versioned_ensembl_gene_id":"ENSG00000283409.1","gene_symbol":"MIR3662","gene_name":"microRNA 3662 [Source:HGNC Symbol;Acc:HGNC:38983]","synonyms":"hsa-mir-3662","biotype":"miRNA","ncbi_id":"100500880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134979338,"end":134979432,"strand":-1,"description":"microRNA 3662 [Source:HGNC Symbol;Acc:HGNC:38983]"}, {"versioned_ensembl_gene_id":"ENSG00000264357.1","gene_symbol":"MIR4648","gene_name":"microRNA 4648 [Source:HGNC Symbol;Acc:HGNC:41560]","synonyms":"hsa-mir-4648","biotype":"miRNA","ncbi_id":"100616116","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2527074,"end":2527145,"strand":1,"description":"microRNA 4648 [Source:HGNC Symbol;Acc:HGNC:41560]"}, {"versioned_ensembl_gene_id":"ENSG00000264249.1","gene_symbol":"MIR3912","gene_name":"microRNA 3912 [Source:HGNC Symbol;Acc:HGNC:38923]","synonyms":"hsa-mir-3912","biotype":"miRNA","ncbi_id":"100500831","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":171386656,"end":171386760,"strand":-1,"description":"microRNA 3912 [Source:HGNC Symbol;Acc:HGNC:38923]"}, {"versioned_ensembl_gene_id":"ENSG00000239822.3","gene_symbol":"RN7SL754P","gene_name":"RNA, 7SL, cytoplasmic 754, pseudogene [Source:HGNC Symbol;Acc:HGNC:46770]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479497","summary":null,"start":430239,"end":430504,"strand":-1,"description":"RNA, 7SL, cytoplasmic 754, pseudogene [Source:HGNC Symbol;Acc:HGNC:46770]"}, {"versioned_ensembl_gene_id":"ENSG00000274046.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7092616,"end":7092716,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199879.1","gene_symbol":"RNU1-120P","gene_name":"RNA, U1 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:48462]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481627","summary":null,"start":148263476,"end":148263632,"strand":1,"description":"RNA, U1 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:48462]"}, {"versioned_ensembl_gene_id":"ENSG00000221763.1","gene_symbol":"MIR1289-1","gene_name":"microRNA 1289-1 [Source:HGNC Symbol;Acc:HGNC:35281]","synonyms":"MIRN1289-1,hsa-mir-1289-1","biotype":"miRNA","ncbi_id":"100302125","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35453954,"end":35454097,"strand":-1,"description":"microRNA 1289-1 [Source:HGNC Symbol;Acc:HGNC:35281]"}, {"versioned_ensembl_gene_id":"ENSG00000202081.1","gene_symbol":"RNU6-1280P","gene_name":"RNA, U6 small nuclear 1280, pseudogene [Source:HGNC Symbol;Acc:HGNC:48243]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481584","summary":null,"start":85651522,"end":85651628,"strand":-1,"description":"RNA, U6 small nuclear 1280, pseudogene [Source:HGNC Symbol;Acc:HGNC:48243]"}, {"versioned_ensembl_gene_id":"ENSG00000278618.1","gene_symbol":"MIR8069-2","gene_name":"microRNA 8069-2 [Source:HGNC Symbol;Acc:HGNC:50836]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504736","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13724189,"end":13724274,"strand":1,"description":"microRNA 8069-2 [Source:HGNC Symbol;Acc:HGNC:50836]"}, {"versioned_ensembl_gene_id":"ENSG00000264075.1","gene_symbol":"MIR4783","gene_name":"microRNA 4783 [Source:HGNC Symbol;Acc:HGNC:41874]","synonyms":"hsa-mir-4783","biotype":"miRNA","ncbi_id":"100616187","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127423537,"end":127423618,"strand":-1,"description":"microRNA 4783 [Source:HGNC Symbol;Acc:HGNC:41874]"}, {"versioned_ensembl_gene_id":"ENSG00000252076.1","gene_symbol":"RN7SKP196","gene_name":"RNA, 7SK small nuclear pseudogene 196 [Source:HGNC Symbol;Acc:HGNC:45920]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479182","summary":null,"start":58869184,"end":58869528,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 196 [Source:HGNC Symbol;Acc:HGNC:45920]"}, {"versioned_ensembl_gene_id":"ENSG00000263510.1","gene_symbol":"MIR4497","gene_name":"microRNA 4497 [Source:HGNC Symbol;Acc:HGNC:41737]","synonyms":"hsa-mir-4497","biotype":"miRNA","ncbi_id":"100616454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109833348,"end":109833436,"strand":1,"description":"microRNA 4497 [Source:HGNC Symbol;Acc:HGNC:41737]"}, {"versioned_ensembl_gene_id":"ENSG00000266555.1","gene_symbol":"MIR3145","gene_name":"microRNA 3145 [Source:HGNC Symbol;Acc:HGNC:38327]","synonyms":"hsa-mir-3145","biotype":"miRNA","ncbi_id":"100423001","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":138435213,"end":138435294,"strand":-1,"description":"microRNA 3145 [Source:HGNC Symbol;Acc:HGNC:38327]"}, {"versioned_ensembl_gene_id":"ENSG00000264986.1","gene_symbol":"MIR5092","gene_name":"microRNA 5092 [Source:HGNC Symbol;Acc:HGNC:43467]","synonyms":"hsa-mir-5092","biotype":"miRNA","ncbi_id":"100847039","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125151465,"end":125151552,"strand":-1,"description":"microRNA 5092 [Source:HGNC Symbol;Acc:HGNC:43467]"}, {"versioned_ensembl_gene_id":"ENSG00000207924.3","gene_symbol":"MIR196A2","gene_name":"microRNA 196a-2 [Source:HGNC Symbol;Acc:HGNC:31568]","synonyms":"MIRN196A2,MIRN196-2,hsa-mir-196a-2,hsa-mir-196-2","biotype":"miRNA","ncbi_id":"406973","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53991738,"end":53991847,"strand":1,"description":"microRNA 196a-2 [Source:HGNC Symbol;Acc:HGNC:31568]"}, {"versioned_ensembl_gene_id":"ENSG00000243015.2","gene_symbol":"RN7SL737P","gene_name":"RNA, 7SL, cytoplasmic 737, pseudogene [Source:HGNC Symbol;Acc:HGNC:46753]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481123","summary":null,"start":93509487,"end":93509768,"strand":1,"description":"RNA, 7SL, cytoplasmic 737, pseudogene [Source:HGNC Symbol;Acc:HGNC:46753]"}, {"versioned_ensembl_gene_id":"ENSG00000202515.1","gene_symbol":"VTRNA1-3","gene_name":"vault RNA 1-3 [Source:HGNC Symbol;Acc:HGNC:12656]","synonyms":"HVG3,hvg-3,vtRNA1-3,VR3,VAULTRC3","biotype":"misc_RNA","ncbi_id":"56662","summary":null,"start":140726158,"end":140726246,"strand":1,"description":"vault RNA 1-3 [Source:HGNC Symbol;Acc:HGNC:12656]"}, {"versioned_ensembl_gene_id":"ENSG00000252305.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":14177131,"end":14177310,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000207798.1","gene_symbol":"MIR216A","gene_name":"microRNA 216a [Source:HGNC Symbol;Acc:HGNC:31593]","synonyms":"MIRN216A,MIRN216,hsa-mir-216a,hsa-mir-216","biotype":"miRNA","ncbi_id":"406998","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55988950,"end":55989059,"strand":-1,"description":"microRNA 216a [Source:HGNC Symbol;Acc:HGNC:31593]"}, {"versioned_ensembl_gene_id":"ENSG00000268674.2","gene_symbol":"FAM231D","gene_name":"family with sequence similarity 231 member D [Source:NCBI gene;Acc:644634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644634","summary":null,"start":35407,"end":35916,"strand":1,"description":"family with sequence similarity 231 member D [Source:NCBI gene;Acc:644634]"}, {"versioned_ensembl_gene_id":"ENSG00000264975.1","gene_symbol":"MIR4431","gene_name":"microRNA 4431 [Source:HGNC Symbol;Acc:HGNC:41738]","synonyms":"hsa-mir-4431","biotype":"miRNA","ncbi_id":"100616431","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52702522,"end":52702615,"strand":-1,"description":"microRNA 4431 [Source:HGNC Symbol;Acc:HGNC:41738]"}, {"versioned_ensembl_gene_id":"ENSG00000201216.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":102950467,"end":102950564,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277845.1","gene_symbol":"RN7SKP175","gene_name":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479173","summary":null,"start":143542110,"end":143542398,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]"}, {"versioned_ensembl_gene_id":"ENSG00000266663.1","gene_symbol":"MIR3169","gene_name":"microRNA 3169 [Source:HGNC Symbol;Acc:HGNC:38380]","synonyms":"hsa-mir-3169","biotype":"miRNA","ncbi_id":"100422973","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61199798,"end":61199880,"strand":-1,"description":"microRNA 3169 [Source:HGNC Symbol;Acc:HGNC:38380]"}, {"versioned_ensembl_gene_id":"ENSG00000283664.1","gene_symbol":"MIR4679-1","gene_name":"microRNA 4679-1 [Source:HGNC Symbol;Acc:HGNC:41612]","synonyms":"hsa-mir-4679-1","biotype":"miRNA","ncbi_id":"100616128","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89063336,"end":89063410,"strand":1,"description":"microRNA 4679-1 [Source:HGNC Symbol;Acc:HGNC:41612]"}, {"versioned_ensembl_gene_id":"ENSG00000207122.1","gene_symbol":"RNU6-591P","gene_name":"RNA, U6 small nuclear 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:47554]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479827","summary":null,"start":39081180,"end":39081285,"strand":-1,"description":"RNA, U6 small nuclear 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:47554]"}, {"versioned_ensembl_gene_id":"ENSG00000212238.1","gene_symbol":"RNA5SP244","gene_name":"RNA, 5S ribosomal pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:43144]","synonyms":"RN5S244","biotype":"rRNA","ncbi_id":"100885864","summary":null,"start":129756266,"end":129756377,"strand":1,"description":"RNA, 5S ribosomal pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:43144]"}, {"versioned_ensembl_gene_id":"ENSG00000201489.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7537096,"end":7537196,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277994.1","gene_symbol":"HOTAIR_3","gene_name":"HOTAIR conserved region 3 [Source:RFAM;Acc:RF01906]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53965965,"end":53966061,"strand":1,"description":"HOTAIR conserved region 3 [Source:RFAM;Acc:RF01906]"}, {"versioned_ensembl_gene_id":"ENSG00000206917.1","gene_symbol":"RNU1-52P","gene_name":"RNA, U1 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48394]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480164","summary":null,"start":58677574,"end":58677737,"strand":-1,"description":"RNA, U1 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48394]"}, {"versioned_ensembl_gene_id":"ENSG00000206722.1","gene_symbol":"RNU6-1074P","gene_name":"RNA, U6 small nuclear 1074, pseudogene [Source:HGNC Symbol;Acc:HGNC:48037]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480635","summary":null,"start":139256657,"end":139256760,"strand":-1,"description":"RNA, U6 small nuclear 1074, pseudogene [Source:HGNC Symbol;Acc:HGNC:48037]"}, {"versioned_ensembl_gene_id":"ENSG00000222950.1","gene_symbol":"RN7SKP262","gene_name":"RNA, 7SK small nuclear pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:45986]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479212","summary":null,"start":25779287,"end":25779569,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:45986]"}, {"versioned_ensembl_gene_id":"ENSG00000244677.3","gene_symbol":"RN7SL706P","gene_name":"RNA, 7SL, cytoplasmic 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:46722]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479480","summary":null,"start":68149617,"end":68149908,"strand":-1,"description":"RNA, 7SL, cytoplasmic 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:46722]"}, {"versioned_ensembl_gene_id":"ENSG00000277922.1","gene_symbol":"FTX_5","gene_name":"FTX transcript, XIST regulator conserved region 5 [Source:RFAM;Acc:RF02122]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74293357,"end":74293574,"strand":1,"description":"FTX transcript, XIST regulator conserved region 5 [Source:RFAM;Acc:RF02122]"}, {"versioned_ensembl_gene_id":"ENSG00000222154.1","gene_symbol":"RN7SKP218","gene_name":"RNA, 7SK small nuclear pseudogene 218 [Source:HGNC Symbol;Acc:HGNC:45942]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480900","summary":null,"start":53490148,"end":53490439,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 218 [Source:HGNC Symbol;Acc:HGNC:45942]"}, {"versioned_ensembl_gene_id":"ENSG00000277752.1","gene_symbol":"DLEU2_5","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50075570,"end":50075653,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]"}, {"versioned_ensembl_gene_id":"ENSG00000276253.1","gene_symbol":"AC243790.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30361040,"end":30361438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221216.1","gene_symbol":"RNU6ATAC27P","gene_name":"RNA, U6atac small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46926]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481167","summary":null,"start":28481362,"end":28481480,"strand":1,"description":"RNA, U6atac small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46926]"}, {"versioned_ensembl_gene_id":"ENSG00000200831.1","gene_symbol":"SNORD36B","gene_name":"small nucleolar RNA, C/D box 36B [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201980.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"E2-1,RNU108,E2,RNE2","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":4756645,"end":4756797,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000251756.1","gene_symbol":"RNA5SP385","gene_name":"RNA, 5S ribosomal pseudogene 385 [Source:HGNC Symbol;Acc:HGNC:43285]","synonyms":"RN5S385","biotype":"rRNA","ncbi_id":"100873640","summary":null,"start":51692752,"end":51692861,"strand":1,"description":"RNA, 5S ribosomal pseudogene 385 [Source:HGNC Symbol;Acc:HGNC:43285]"}, {"versioned_ensembl_gene_id":"ENSG00000244307.3","gene_symbol":"RN7SL395P","gene_name":"RNA, 7SL, cytoplasmic 395, pseudogene [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93483936,"end":93484019,"strand":-1,"description":"microRNA 489 [Source:HGNC Symbol;Acc:HGNC:32074]"}, {"versioned_ensembl_gene_id":"ENSG00000198995.3","gene_symbol":"MIR340","gene_name":"microRNA 340 [Source:HGNC Symbol;Acc:HGNC:31777]","synonyms":"MIRN340,hsa-mir-340","biotype":"miRNA","ncbi_id":"442908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":180015303,"end":180015397,"strand":-1,"description":"microRNA 340 [Source:HGNC Symbol;Acc:HGNC:31777]"}, {"versioned_ensembl_gene_id":"ENSG00000201511.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101647421,"end":101647522,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207428.1","gene_symbol":"RNU6-95P","gene_name":"RNA, U6 small nuclear 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:47058]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479608","summary":null,"start":68003895,"end":68004001,"strand":1,"description":"RNA, U6 small nuclear 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:47058]"}, {"versioned_ensembl_gene_id":"ENSG00000216058.1","gene_symbol":"MIR944","gene_name":"microRNA 944 [Source:HGNC Symbol;Acc:HGNC:33690]","synonyms":"MIRN944,hsa-mir-944","biotype":"miRNA","ncbi_id":"100126340","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":189829922,"end":189830009,"strand":1,"description":"microRNA 944 [Source:HGNC Symbol;Acc:HGNC:33690]"}, {"versioned_ensembl_gene_id":"ENSG00000273818.1","gene_symbol":"RN7SL673P","gene_name":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480525","summary":null,"start":30091662,"end":30091898,"strand":1,"description":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]"}, {"versioned_ensembl_gene_id":"ENSG00000207041.1","gene_symbol":"RNU6-3P","gene_name":"RNA, U6 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34275]","synonyms":"U6-3,RNU6-3","biotype":"snRNA","ncbi_id":"106478919","summary":null,"start":141118030,"end":141118136,"strand":-1,"description":"RNA, U6 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34275]"}, {"versioned_ensembl_gene_id":"ENSG00000201223.1","gene_symbol":"RNU6-1305P","gene_name":"RNA, U6 small nuclear 1305, pseudogene [Source:HGNC Symbol;Acc:HGNC:48268]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481592","summary":null,"start":36155119,"end":36155222,"strand":1,"description":"RNA, U6 small nuclear 1305, pseudogene [Source:HGNC Symbol;Acc:HGNC:48268]"}, {"versioned_ensembl_gene_id":"ENSG00000253287.1","gene_symbol":"AC104012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71779605,"end":71792875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284448.1","gene_symbol":"MIR6501","gene_name":"microRNA 6501 [Source:HGNC Symbol;Acc:HGNC:50033]","synonyms":"hsa-mir-6501","biotype":"miRNA","ncbi_id":"102465248","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33550662,"end":33550728,"strand":1,"description":"microRNA 6501 [Source:HGNC Symbol;Acc:HGNC:50033]"}, {"versioned_ensembl_gene_id":"ENSG00000199832.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":107202577,"end":107202683,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275458.1","gene_symbol":"MIR6809","gene_name":"microRNA 6809 [Source:HGNC Symbol;Acc:HGNC:49926]","synonyms":"hsa-mir-6809","biotype":"miRNA","ncbi_id":"102465485","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":217900513,"end":217900628,"strand":-1,"description":"microRNA 6809 [Source:HGNC Symbol;Acc:HGNC:49926]"}, {"versioned_ensembl_gene_id":"ENSG00000273752.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54855316,"end":54855422,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000284067.1","gene_symbol":"MIR6837","gene_name":"microRNA 6837 [Source:HGNC Symbol;Acc:HGNC:50125]","synonyms":"hsa-mir-6837","biotype":"miRNA","ncbi_id":"102466985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44051766,"end":44051829,"strand":1,"description":"microRNA 6837 [Source:HGNC Symbol;Acc:HGNC:50125]"}, {"versioned_ensembl_gene_id":"ENSG00000200455.1","gene_symbol":"RNU6-1112P","gene_name":"RNA, U6 small nuclear 1112, pseudogene [Source:HGNC Symbol;Acc:HGNC:48075]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480055","summary":null,"start":40077884,"end":40077982,"strand":1,"description":"RNA, U6 small nuclear 1112, pseudogene [Source:HGNC Symbol;Acc:HGNC:48075]"}, {"versioned_ensembl_gene_id":"ENSG00000221288.1","gene_symbol":"MIR663B","gene_name":"microRNA 663b [Source:HGNC Symbol;Acc:HGNC:35270]","synonyms":"MIRN663B,hsa-mir-663b","biotype":"miRNA","ncbi_id":"100313824","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132256966,"end":132257080,"strand":-1,"description":"microRNA 663b [Source:HGNC Symbol;Acc:HGNC:35270]"}, {"versioned_ensembl_gene_id":"ENSG00000207645.2","gene_symbol":"MIR512-1","gene_name":"microRNA 512-1 [Source:HGNC Symbol;Acc:HGNC:32090]","synonyms":"hsa-mir-512-1,MIRN512-1","biotype":"miRNA","ncbi_id":"574458","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53666679,"end":53666762,"strand":1,"description":"microRNA 512-1 [Source:HGNC Symbol;Acc:HGNC:32090]"}, {"versioned_ensembl_gene_id":"ENSG00000199047.3","gene_symbol":"MIR378A","gene_name":"microRNA 378a [Source:HGNC Symbol;Acc:HGNC:31871]","synonyms":"hsa-mir-378,MIRN378,MIR378","biotype":"miRNA","ncbi_id":"494327","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149732825,"end":149732890,"strand":1,"description":"microRNA 378a [Source:HGNC Symbol;Acc:HGNC:31871]"}, {"versioned_ensembl_gene_id":"ENSG00000199792.1","gene_symbol":"RNU6-1233P","gene_name":"RNA, U6 small nuclear 1233, pseudogene [Source:HGNC Symbol;Acc:HGNC:48196]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481569","summary":null,"start":175397247,"end":175397348,"strand":-1,"description":"RNA, U6 small nuclear 1233, pseudogene [Source:HGNC Symbol;Acc:HGNC:48196]"}, {"versioned_ensembl_gene_id":"ENSG00000236360.2","gene_symbol":"AL445183.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52993201,"end":52993702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274390.1","gene_symbol":"MIR6885","gene_name":"microRNA 6885 [Source:HGNC Symbol;Acc:HGNC:50221]","synonyms":"hsa-mir-6885","biotype":"miRNA","ncbi_id":"102465533","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6389638,"end":6389703,"strand":-1,"description":"microRNA 6885 [Source:HGNC Symbol;Acc:HGNC:50221]"}, {"versioned_ensembl_gene_id":"ENSG00000238562.1","gene_symbol":"RNU7-159P","gene_name":"RNA, U7 small nuclear 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:45693]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481747","summary":null,"start":102903892,"end":102903953,"strand":-1,"description":"RNA, U7 small nuclear 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:45693]"}, {"versioned_ensembl_gene_id":"ENSG00000264233.1","gene_symbol":"MIR4456","gene_name":"microRNA 4456 [Source:HGNC Symbol;Acc:HGNC:41606]","synonyms":"hsa-mir-4456","biotype":"miRNA","ncbi_id":"100616381","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":535840,"end":535882,"strand":-1,"description":"microRNA 4456 [Source:HGNC Symbol;Acc:HGNC:41606]"}, {"versioned_ensembl_gene_id":"ENSG00000266146.1","gene_symbol":"MIR5190","gene_name":"microRNA 5190 [Source:HGNC Symbol;Acc:HGNC:43549]","synonyms":"hsa-mir-5190","biotype":"miRNA","ncbi_id":"100847080","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13459947,"end":13460026,"strand":1,"description":"microRNA 5190 [Source:HGNC Symbol;Acc:HGNC:43549]"}, {"versioned_ensembl_gene_id":"ENSG00000263955.2","gene_symbol":"RN7SL850P","gene_name":"RNA, 7SL, cytoplasmic 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:46866]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479532","summary":null,"start":4633591,"end":4633881,"strand":-1,"description":"RNA, 7SL, cytoplasmic 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:46866]"}, {"versioned_ensembl_gene_id":"ENSG00000212624.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":51724775,"end":51724896,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000278250.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":120018900,"end":120019261,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283744.1","gene_symbol":"MIR6755","gene_name":"microRNA 6755 [Source:HGNC Symbol;Acc:HGNC:50224]","synonyms":"hsa-mir-6755","biotype":"miRNA","ncbi_id":"102465452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86278333,"end":86278398,"strand":1,"description":"microRNA 6755 [Source:HGNC Symbol;Acc:HGNC:50224]"}, {"versioned_ensembl_gene_id":"ENSG00000266439.2","gene_symbol":"RN7SL493P","gene_name":"RNA, 7SL, cytoplasmic 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:46509]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479403","summary":null,"start":10221775,"end":10222073,"strand":-1,"description":"RNA, 7SL, cytoplasmic 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:46509]"}, {"versioned_ensembl_gene_id":"ENSG00000263912.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30743271,"end":30743522,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000274284.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38231043,"end":38231144,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000262579.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":69175662,"end":69175768,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000276222.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46226740,"end":46226841,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201415.1","gene_symbol":"RNA5SP204","gene_name":"RNA, 5S ribosomal pseudogene 204 [Source:HGNC Symbol;Acc:HGNC:43104]","synonyms":"RN5S204","biotype":"rRNA","ncbi_id":"100873465","summary":null,"start":17721786,"end":17721903,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 204 [Source:HGNC Symbol;Acc:HGNC:43104]"}, {"versioned_ensembl_gene_id":"ENSG00000263908.1","gene_symbol":"MIR3116-1","gene_name":"microRNA 3116-1 [Source:HGNC Symbol;Acc:HGNC:38200]","synonyms":"hsa-mir-3116-1","biotype":"miRNA","ncbi_id":"100422902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62078786,"end":62078859,"strand":1,"description":"microRNA 3116-1 [Source:HGNC Symbol;Acc:HGNC:38200]"}, {"versioned_ensembl_gene_id":"ENSG00000266203.1","gene_symbol":"MIR5585","gene_name":"microRNA 5585 [Source:HGNC Symbol;Acc:HGNC:43452]","synonyms":"hsa-mir-5585","biotype":"miRNA","ncbi_id":"100847018","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32086949,"end":32087007,"strand":1,"description":"microRNA 5585 [Source:HGNC Symbol;Acc:HGNC:43452]"}, {"versioned_ensembl_gene_id":"ENSG00000206911.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93827622,"end":93827734,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278124.1","gene_symbol":"RN7SL186P","gene_name":"RNA, 7SL, cytoplasmic 186, pseudogene [Source:HGNC Symbol;Acc:HGNC:46202]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480972","summary":null,"start":22010650,"end":22010946,"strand":1,"description":"RNA, 7SL, cytoplasmic 186, pseudogene [Source:HGNC Symbol;Acc:HGNC:46202]"}, {"versioned_ensembl_gene_id":"ENSG00000199469.1","gene_symbol":"RNU1-62P","gene_name":"RNA, U1 small nuclear 62, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000199934.1","gene_symbol":"SNORD81","gene_name":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]","synonyms":null,"biotype":"snoRNA","ncbi_id":"26769","summary":null,"start":85592280,"end":85592356,"strand":1,"description":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]"}, {"versioned_ensembl_gene_id":"ENSG00000201710.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100979992,"end":100980066,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000243900.3","gene_symbol":"RN7SL320P","gene_name":"RNA, 7SL, cytoplasmic 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:46336]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481010","summary":null,"start":51469753,"end":51470047,"strand":1,"description":"RNA, 7SL, cytoplasmic 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:46336]"}, {"versioned_ensembl_gene_id":"ENSG00000276918.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66374138,"end":66374435,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277653.1","gene_symbol":"CDKN2B-AS","gene_name":"CDKN2B antisense RNA 1 intronic convserved region [Source:RFAM;Acc:RF01909]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22117665,"end":22117814,"strand":1,"description":"CDKN2B antisense RNA 1 intronic convserved region [Source:RFAM;Acc:RF01909]"}, {"versioned_ensembl_gene_id":"ENSG00000251705.1","gene_symbol":"RNA5-8SP6","gene_name":"RNA, 5.8S ribosomal pseudogene 6 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000272075.2","gene_symbol":"RN7SL828P","gene_name":"RNA, 7SL, cytoplasmic 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:46844]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481147","summary":null,"start":118067237,"end":118067539,"strand":1,"description":"RNA, 7SL, cytoplasmic 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:46844]"}, {"versioned_ensembl_gene_id":"ENSG00000277542.1","gene_symbol":"HOXB13-AS1_2","gene_name":"HOXB13 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02133]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48723692,"end":48723772,"strand":1,"description":"HOXB13 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02133]"}, {"versioned_ensembl_gene_id":"ENSG00000278123.1","gene_symbol":"SNORD116-28","gene_name":"small nucleolar RNA, C/D box 116-28 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000244512.3","gene_symbol":"RN7SL28P","gene_name":"RNA, 7SL, cytoplasmic 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46044]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480929","summary":null,"start":184278936,"end":184279233,"strand":1,"description":"RNA, 7SL, cytoplasmic 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46044]"}, {"versioned_ensembl_gene_id":"ENSG00000203573.4","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40585454,"end":40585751,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212579.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 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{"versioned_ensembl_gene_id":"ENSG00000273642.1","gene_symbol":"AC012314.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251859.1","gene_symbol":"RNU6-1288P","gene_name":"RNA, U6 small nuclear 1288, pseudogene [Source:HGNC Symbol;Acc:HGNC:48251]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480128","summary":null,"start":14274622,"end":14274725,"strand":-1,"description":"RNA, U6 small nuclear 1288, pseudogene [Source:HGNC Symbol;Acc:HGNC:48251]"}, {"versioned_ensembl_gene_id":"ENSG00000284317.1","gene_symbol":"MIR7114","gene_name":"microRNA 7114 [Source:HGNC Symbol;Acc:HGNC:50157]","synonyms":"hsa-mir-7114","biotype":"miRNA","ncbi_id":"102466223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":137450026,"end":137450086,"strand":-1,"description":"microRNA 7114 [Source:HGNC Symbol;Acc:HGNC:50157]"}, {"versioned_ensembl_gene_id":"ENSG00000252426.1","gene_symbol":"RNU1-107P","gene_name":"RNA, U1 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48449]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480186","summary":null,"start":25723342,"end":25723495,"strand":1,"description":"RNA, U1 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48449]"}, {"versioned_ensembl_gene_id":"ENSG00000207380.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":5964538,"end":5964650,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201325.1","gene_symbol":"RNA5SP142","gene_name":"RNA, 5S ribosomal pseudogene 142 [Source:HGNC Symbol;Acc:HGNC:43042]","synonyms":"RN5S142","biotype":"rRNA","ncbi_id":"100873409","summary":null,"start":137518134,"end":137518255,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 142 [Source:HGNC Symbol;Acc:HGNC:43042]"}, {"versioned_ensembl_gene_id":"ENSG00000221275.1","gene_symbol":"MIR548I2","gene_name":"microRNA 548i-2 [Source:HGNC Symbol;Acc:HGNC:35353]","synonyms":"MIRN548I2,hsa-mir-548i-2","biotype":"miRNA","ncbi_id":"100302277","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9556168,"end":9556316,"strand":-1,"description":"microRNA 548i-2 [Source:HGNC Symbol;Acc:HGNC:35353]"}, {"versioned_ensembl_gene_id":"ENSG00000252468.1","gene_symbol":"RNU2-57P","gene_name":"RNA, U2 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48550]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480222","summary":null,"start":5019076,"end":5019266,"strand":1,"description":"RNA, U2 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48550]"}, {"versioned_ensembl_gene_id":"ENSG00000266780.1","gene_symbol":"MIR4444-2","gene_name":"microRNA 4444-2 [Source:HGNC Symbol;Acc:HGNC:43481]","synonyms":"hsa-mir-4444-2","biotype":"miRNA","ncbi_id":"100846999","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75214476,"end":75214549,"strand":1,"description":"microRNA 4444-2 [Source:HGNC Symbol;Acc:HGNC:43481]"}, {"versioned_ensembl_gene_id":"ENSG00000275708.1","gene_symbol":"MIR3648-1","gene_name":"microRNA 3648-1 [Source:HGNC Symbol;Acc:HGNC:38941]","synonyms":"MIR3648,hsa-mir-3648","biotype":"miRNA","ncbi_id":"100500862","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8208473,"end":8208652,"strand":1,"description":"microRNA 3648-1 [Source:HGNC Symbol;Acc:HGNC:38941]"}, {"versioned_ensembl_gene_id":"ENSG00000199350.1","gene_symbol":"RNA5SP432","gene_name":"RNA, 5S ribosomal pseudogene 432 [Source:HGNC Symbol;Acc:HGNC:43332]","synonyms":"RN5S432","biotype":"rRNA","ncbi_id":"100873682","summary":null,"start":84039918,"end":84040033,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 432 [Source:HGNC Symbol;Acc:HGNC:43332]"}, {"versioned_ensembl_gene_id":"ENSG00000252699.1","gene_symbol":"SNORA21B","gene_name":"small nucleolar RNA, H/ACA box 21B [Source:HGNC Symbol;Acc:HGNC:52195]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617002","summary":null,"start":38851524,"end":38851659,"strand":-1,"description":"small nucleolar RNA, H/ACA box 21B [Source:HGNC Symbol;Acc:HGNC:52195]"}, {"versioned_ensembl_gene_id":"ENSG00000221628.1","gene_symbol":"MIR1302-4","gene_name":"microRNA 1302-4 [Source:HGNC Symbol;Acc:HGNC:35296]","synonyms":"MIRN1302-4,hsa-mir-1302-4","biotype":"miRNA","ncbi_id":"100302130","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207269275,"end":207269424,"strand":-1,"description":"microRNA 1302-4 [Source:HGNC Symbol;Acc:HGNC:35296]"}, {"versioned_ensembl_gene_id":"ENSG00000207513.1","gene_symbol":"RNU1-3","gene_name":"RNA, U1 small nuclear 3 [Source:HGNC Symbol;Acc:HGNC:10130]","synonyms":"HSD4,RNU1G3","biotype":"snRNA","ncbi_id":"26869","summary":null,"start":16666785,"end":16666948,"strand":-1,"description":"RNA, U1 small nuclear 3 [Source:HGNC Symbol;Acc:HGNC:10130]"}, {"versioned_ensembl_gene_id":"ENSG00000207653.1","gene_symbol":"MIR558","gene_name":"microRNA 558 [Source:HGNC Symbol;Acc:HGNC:32814]","synonyms":"MIRN558,hsa-mir-558","biotype":"miRNA","ncbi_id":"693143","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32532153,"end":32532246,"strand":1,"description":"microRNA 558 [Source:HGNC Symbol;Acc:HGNC:32814]"}, {"versioned_ensembl_gene_id":"ENSG00000201377.1","gene_symbol":"RNY4P23","gene_name":"RNA, Ro-associated Y4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42473]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873801","summary":null,"start":70396279,"end":70396375,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42473]"}, {"versioned_ensembl_gene_id":"ENSG00000277887.1","gene_symbol":"SNORA50C","gene_name":"small nucleolar RNA, H/ACA box 50C [Source:HGNC Symbol;Acc:HGNC:32662]","synonyms":"SNORA76C,SNORA76,ACA62","biotype":"snoRNA","ncbi_id":"677842","summary":null,"start":64146339,"end":64146471,"strand":1,"description":"small nucleolar RNA, H/ACA box 50C [Source:HGNC Symbol;Acc:HGNC:32662]"}, {"versioned_ensembl_gene_id":"ENSG00000221548.1","gene_symbol":"MIR1283-2","gene_name":"microRNA 1283-2 [Source:HGNC Symbol;Acc:HGNC:35361]","synonyms":"MIRN1283-2,hsa-mir-1283-2","biotype":"miRNA","ncbi_id":"100302205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53758232,"end":53758318,"strand":1,"description":"microRNA 1283-2 [Source:HGNC Symbol;Acc:HGNC:35361]"}, {"versioned_ensembl_gene_id":"ENSG00000284361.1","gene_symbol":"MIR4745","gene_name":"microRNA 4745 [Source:HGNC Symbol;Acc:HGNC:41868]","synonyms":"hsa-mir-4745","biotype":"miRNA","ncbi_id":"100616459","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":804940,"end":805001,"strand":1,"description":"microRNA 4745 [Source:HGNC Symbol;Acc:HGNC:41868]"}, {"versioned_ensembl_gene_id":"ENSG00000207031.1","gene_symbol":"SNORD59A","gene_name":"small nucleolar RNA, C/D box 59A [Source:HGNC Symbol;Acc:HGNC:10210]","synonyms":"U59,RNU59","biotype":"snoRNA","ncbi_id":"26789","summary":null,"start":56645027,"end":56645101,"strand":-1,"description":"small nucleolar RNA, C/D box 59A [Source:HGNC Symbol;Acc:HGNC:10210]"}, {"versioned_ensembl_gene_id":"ENSG00000207378.1","gene_symbol":"RNU6-748P","gene_name":"RNA, U6 small nuclear 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:47711]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481416","summary":null,"start":98462944,"end":98463050,"strand":-1,"description":"RNA, U6 small nuclear 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:47711]"}, {"versioned_ensembl_gene_id":"ENSG00000201287.1","gene_symbol":"RN7SKP171","gene_name":"RNA, 7SK small nuclear pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:45895]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480887","summary":null,"start":37661747,"end":37662049,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:45895]"}, {"versioned_ensembl_gene_id":"ENSG00000274655.1","gene_symbol":"XIST_intron","gene_name":"XIST 3' intron conserved motif [Source:RFAM;Acc:RF02266]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73821657,"end":73821724,"strand":-1,"description":"XIST 3' intron conserved motif [Source:RFAM;Acc:RF02266]"}, {"versioned_ensembl_gene_id":"ENSG00000283172.1","gene_symbol":"hsa-mir-548d-1","gene_name":"hsa-mir-548d-1 [Source:miRBase;Acc:MI0003668]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":123348034,"end":123348130,"strand":-1,"description":"hsa-mir-548d-1 [Source:miRBase;Acc:MI0003668]"}, {"versioned_ensembl_gene_id":"ENSG00000202542.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48325558,"end":48325671,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265635.1","gene_symbol":"MIR3612","gene_name":"microRNA 3612 [Source:HGNC Symbol;Acc:HGNC:38951]","synonyms":"hsa-mir-3612","biotype":"miRNA","ncbi_id":"100500817","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128294092,"end":128294178,"strand":1,"description":"microRNA 3612 [Source:HGNC Symbol;Acc:HGNC:38951]"}, {"versioned_ensembl_gene_id":"ENSG00000253005.1","gene_symbol":"RNU6-176P","gene_name":"RNA, U6 small nuclear 176, pseudogene [Source:HGNC Symbol;Acc:HGNC:47139]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479644","summary":null,"start":28142737,"end":28142841,"strand":-1,"description":"RNA, U6 small nuclear 176, pseudogene [Source:HGNC Symbol;Acc:HGNC:47139]"}, {"versioned_ensembl_gene_id":"ENSG00000276622.1","gene_symbol":"MIR6499","gene_name":"microRNA 6499 [Source:HGNC Symbol;Acc:HGNC:49962]","synonyms":"hsa-mir-6499","biotype":"miRNA","ncbi_id":"102465246","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151522087,"end":151522148,"strand":-1,"description":"microRNA 6499 [Source:HGNC Symbol;Acc:HGNC:49962]"}, {"versioned_ensembl_gene_id":"ENSG00000239041.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":172691299,"end":172691402,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000265345.1","gene_symbol":"MIR5188","gene_name":"microRNA 5188 [Source:HGNC Symbol;Acc:HGNC:43502]","synonyms":"hsa-mir-5188","biotype":"miRNA","ncbi_id":"100847004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124915547,"end":124915659,"strand":1,"description":"microRNA 5188 [Source:HGNC Symbol;Acc:HGNC:43502]"}, {"versioned_ensembl_gene_id":"ENSG00000276220.1","gene_symbol":"AC012314.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212450.1","gene_symbol":"RNU6-241P","gene_name":"RNA, U6 small nuclear 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:47204]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479674","summary":null,"start":45789585,"end":45789688,"strand":1,"description":"RNA, U6 small nuclear 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:47204]"}, {"versioned_ensembl_gene_id":"ENSG00000276507.1","gene_symbol":"AC068944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29010619,"end":29011021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265357.1","gene_symbol":"MIR4493","gene_name":"microRNA 4493 [Source:HGNC Symbol;Acc:HGNC:41778]","synonyms":"hsa-mir-4493","biotype":"miRNA","ncbi_id":"100616319","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123381440,"end":123381512,"strand":-1,"description":"microRNA 4493 [Source:HGNC Symbol;Acc:HGNC:41778]"}, {"versioned_ensembl_gene_id":"ENSG00000253065.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":168033091,"end":168033205,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000272036.1","gene_symbol":"MIR139","gene_name":"microRNA 139 [Source:HGNC Symbol;Acc:HGNC:31526]","synonyms":"MIRN139,hsa-mir-139","biotype":"miRNA","ncbi_id":"406931","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72615063,"end":72615130,"strand":-1,"description":"microRNA 139 [Source:HGNC Symbol;Acc:HGNC:31526]"}, {"versioned_ensembl_gene_id":"ENSG00000207133.1","gene_symbol":"SNORD116-7","gene_name":"small nucleolar RNA, C/D box 116-7 [Source:HGNC Symbol;Acc:HGNC:33073]","synonyms":"HBII-85-7","biotype":"snoRNA","ncbi_id":"100033419","summary":null,"start":25067788,"end":25067882,"strand":1,"description":"small nucleolar RNA, C/D box 116-7 [Source:HGNC Symbol;Acc:HGNC:33073]"}, {"versioned_ensembl_gene_id":"ENSG00000223305.1","gene_symbol":"RN7SKP30","gene_name":"RNA, 7SK small nuclear pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45754]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479108","summary":null,"start":55540502,"end":55540835,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45754]"}, {"versioned_ensembl_gene_id":"ENSG00000266666.1","gene_symbol":"MIR4325","gene_name":"microRNA 4325 [Source:HGNC Symbol;Acc:HGNC:38304]","synonyms":"hsa-mir-4325","biotype":"miRNA","ncbi_id":"100422883","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57321502,"end":57321591,"strand":-1,"description":"microRNA 4325 [Source:HGNC Symbol;Acc:HGNC:38304]"}, {"versioned_ensembl_gene_id":"ENSG00000264559.1","gene_symbol":"MIR3162","gene_name":"microRNA 3162 [Source:HGNC Symbol;Acc:HGNC:38271]","synonyms":"hsa-mir-3162","biotype":"miRNA","ncbi_id":"100422880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59595077,"end":59595158,"strand":-1,"description":"microRNA 3162 [Source:HGNC Symbol;Acc:HGNC:38271]"}, {"versioned_ensembl_gene_id":"ENSG00000199575.1","gene_symbol":"SNORD114-1","gene_name":"small nucleolar RNA, C/D box 114-1 [Source:HGNC Symbol;Acc:HGNC:32989]","synonyms":"14q(II-1)","biotype":"snoRNA","ncbi_id":"767577","summary":"Small nucleolar RNAs (snoRNAs), like SNORD114-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD114-1 is 1 of 31 tandem SNORD114 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":100949833,"end":100949904,"strand":1,"description":"small nucleolar RNA, C/D box 114-1 [Source:HGNC Symbol;Acc:HGNC:32989]"}, {"versioned_ensembl_gene_id":"ENSG00000261867.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":101205448,"end":101205554,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000212520.1","gene_symbol":"RNU6-1250P","gene_name":"RNA, U6 small nuclear 1250, pseudogene [Source:HGNC Symbol;Acc:HGNC:48213]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481575","summary":null,"start":67808502,"end":67808608,"strand":1,"description":"RNA, U6 small nuclear 1250, pseudogene [Source:HGNC Symbol;Acc:HGNC:48213]"}, {"versioned_ensembl_gene_id":"ENSG00000199065.3","gene_symbol":"MIR101-2","gene_name":"microRNA 101-2 [Source:HGNC Symbol;Acc:HGNC:31489]","synonyms":"hsa-mir-101-2,MIRN101-2","biotype":"miRNA","ncbi_id":"406894","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4850297,"end":4850375,"strand":1,"description":"microRNA 101-2 [Source:HGNC Symbol;Acc:HGNC:31489]"}, {"versioned_ensembl_gene_id":"ENSG00000212133.1","gene_symbol":"RNU6-1168P","gene_name":"RNA, U6 small nuclear 1168, pseudogene [Source:HGNC Symbol;Acc:HGNC:48131]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481548","summary":null,"start":88383494,"end":88383597,"strand":-1,"description":"RNA, U6 small nuclear 1168, pseudogene [Source:HGNC Symbol;Acc:HGNC:48131]"}, {"versioned_ensembl_gene_id":"ENSG00000200427.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85777639,"end":85777755,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265331.1","gene_symbol":"MIR4524B","gene_name":"microRNA 4524b [Source:HGNC Symbol;Acc:HGNC:43520]","synonyms":"hsa-mir-4524b","biotype":"miRNA","ncbi_id":"100847008","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69099542,"end":69099656,"strand":1,"description":"microRNA 4524b [Source:HGNC Symbol;Acc:HGNC:43520]"}, {"versioned_ensembl_gene_id":"ENSG00000277202.1","gene_symbol":"MIR8063","gene_name":"microRNA 8063 [Source:HGNC Symbol;Acc:HGNC:50088]","synonyms":"hsa-mir-8063","biotype":"miRNA","ncbi_id":"102466875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36972821,"end":36972901,"strand":-1,"description":"microRNA 8063 [Source:HGNC Symbol;Acc:HGNC:50088]"}, {"versioned_ensembl_gene_id":"ENSG00000200737.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97421195,"end":97421307,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264500.1","gene_symbol":"MIR3124","gene_name":"microRNA 3124 [Source:HGNC Symbol;Acc:HGNC:38262]","synonyms":"hsa-mir-3124","biotype":"miRNA","ncbi_id":"100422879","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":248826377,"end":248826443,"strand":1,"description":"microRNA 3124 [Source:HGNC Symbol;Acc:HGNC:38262]"}, {"versioned_ensembl_gene_id":"ENSG00000276640.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30136615,"end":30136690,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000241552.3","gene_symbol":"RN7SL58P","gene_name":"RNA, 7SL, cytoplasmic 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:46074]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479245","summary":null,"start":18547312,"end":18547605,"strand":1,"description":"RNA, 7SL, cytoplasmic 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:46074]"}, {"versioned_ensembl_gene_id":"ENSG00000225091.3","gene_symbol":"SNORA71A","gene_name":"small nucleolar RNA, H/ACA box 71A [Source:HGNC Symbol;Acc:HGNC:10232]","synonyms":"U71a,RNU71A","biotype":"snoRNA","ncbi_id":"26777","summary":null,"start":38427309,"end":38427442,"strand":-1,"description":"small nucleolar RNA, H/ACA box 71A [Source:HGNC Symbol;Acc:HGNC:10232]"}, {"versioned_ensembl_gene_id":"ENSG00000265932.1","gene_symbol":"MIR3146","gene_name":"microRNA 3146 [Source:HGNC Symbol;Acc:HGNC:38368]","synonyms":"hsa-mir-3146","biotype":"miRNA","ncbi_id":"100422967","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19705358,"end":19705436,"strand":-1,"description":"microRNA 3146 [Source:HGNC Symbol;Acc:HGNC:38368]"}, {"versioned_ensembl_gene_id":"ENSG00000207607.3","gene_symbol":"MIR200A","gene_name":"microRNA 200a [Source:HGNC Symbol;Acc:HGNC:31578]","synonyms":"MIRN200A,hsa-mir-200a","biotype":"miRNA","ncbi_id":"406983","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1167863,"end":1167952,"strand":1,"description":"microRNA 200a [Source:HGNC Symbol;Acc:HGNC:31578]"}, {"versioned_ensembl_gene_id":"ENSG00000243125.3","gene_symbol":"RN7SL807P","gene_name":"RNA, 7SL, cytoplasmic 807, pseudogene [Source:HGNC Symbol;Acc:HGNC:46823]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481141","summary":null,"start":223248498,"end":223248794,"strand":-1,"description":"RNA, 7SL, cytoplasmic 807, pseudogene [Source:HGNC Symbol;Acc:HGNC:46823]"}, {"versioned_ensembl_gene_id":"ENSG00000223056.1","gene_symbol":"RN7SKP169","gene_name":"RNA, 7SK small nuclear pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:45893]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480886","summary":null,"start":25963983,"end":25964273,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:45893]"}, {"versioned_ensembl_gene_id":"ENSG00000207327.1","gene_symbol":"RNU6-883P","gene_name":"RNA, U6 small nuclear 883, pseudogene [Source:HGNC Symbol;Acc:HGNC:47846]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481921","summary":null,"start":73529051,"end":73529157,"strand":-1,"description":"RNA, U6 small nuclear 883, pseudogene [Source:HGNC Symbol;Acc:HGNC:47846]"}, {"versioned_ensembl_gene_id":"ENSG00000273927.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73039085,"end":73039186,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252491.1","gene_symbol":"RNU1-142P","gene_name":"RNA, U1 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:48484]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480197","summary":null,"start":26790142,"end":26790286,"strand":1,"description":"RNA, U1 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:48484]"}, {"versioned_ensembl_gene_id":"ENSG00000260454.1","gene_symbol":"AL355607.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90997054,"end":91001871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266415.1","gene_symbol":"MIR4636","gene_name":"microRNA 4636 [Source:HGNC Symbol;Acc:HGNC:41798]","synonyms":"hsa-mir-4636","biotype":"miRNA","ncbi_id":"100616326","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9053816,"end":9053895,"strand":-1,"description":"microRNA 4636 [Source:HGNC Symbol;Acc:HGNC:41798]"}, {"versioned_ensembl_gene_id":"ENSG00000279049.1","gene_symbol":"AL353898.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":54099968,"end":54100224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207452.1","gene_symbol":"RNU6-606P","gene_name":"RNA, U6 small nuclear 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:47569]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479834","summary":null,"start":87299687,"end":87299797,"strand":-1,"description":"RNA, U6 small nuclear 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:47569]"}, {"versioned_ensembl_gene_id":"ENSG00000207042.1","gene_symbol":"RNU6-196P","gene_name":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481238","summary":null,"start":21642294,"end":21642400,"strand":1,"description":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]"}, {"versioned_ensembl_gene_id":"ENSG00000278278.1","gene_symbol":"MIR6816","gene_name":"microRNA 6816 [Source:HGNC Symbol;Acc:HGNC:50256]","synonyms":"hsa-mir-6816","biotype":"miRNA","ncbi_id":"102465490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20114686,"end":20114751,"strand":-1,"description":"microRNA 6816 [Source:HGNC Symbol;Acc:HGNC:50256]"}, {"versioned_ensembl_gene_id":"ENSG00000278469.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3124777,"end":3125063,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266436.1","gene_symbol":"MIR4264","gene_name":"microRNA 4264 [Source:HGNC Symbol;Acc:HGNC:38338]","synonyms":"hsa-mir-4264","biotype":"miRNA","ncbi_id":"100422888","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79649294,"end":79649359,"strand":-1,"description":"microRNA 4264 [Source:HGNC Symbol;Acc:HGNC:38338]"}, {"versioned_ensembl_gene_id":"ENSG00000206716.1","gene_symbol":"RNU6-133P","gene_name":"RNA, U6 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:47096]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481877","summary":null,"start":21214637,"end":21214743,"strand":1,"description":"RNA, U6 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:47096]"}, {"versioned_ensembl_gene_id":"ENSG00000206925.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40342329,"end":40342441,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264049.1","gene_symbol":"MIR4737","gene_name":"microRNA 4737 [Source:HGNC Symbol;Acc:HGNC:41669]","synonyms":"hsa-mir-4737","biotype":"miRNA","ncbi_id":"100616210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60043025,"end":60043105,"strand":-1,"description":"microRNA 4737 [Source:HGNC Symbol;Acc:HGNC:41669]"}, {"versioned_ensembl_gene_id":"ENSG00000251980.1","gene_symbol":"RNU6-436P","gene_name":"RNA, U6 small nuclear 436, pseudogene [Source:HGNC Symbol;Acc:HGNC:47399]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481316","summary":null,"start":157912772,"end":157912885,"strand":1,"description":"RNA, U6 small nuclear 436, pseudogene [Source:HGNC Symbol;Acc:HGNC:47399]"}, {"versioned_ensembl_gene_id":"ENSG00000201078.1","gene_symbol":"RN7SKP214","gene_name":"RNA, 7SK small nuclear pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:45938]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480473","summary":null,"start":37055033,"end":37055347,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:45938]"}, {"versioned_ensembl_gene_id":"ENSG00000274860.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6521131,"end":6521412,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207287.1","gene_symbol":"RNU6-1274P","gene_name":"RNA, U6 small nuclear 1274, pseudogene [Source:HGNC Symbol;Acc:HGNC:48237]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481582","summary":null,"start":96743167,"end":96743273,"strand":1,"description":"RNA, U6 small nuclear 1274, pseudogene [Source:HGNC Symbol;Acc:HGNC:48237]"}, {"versioned_ensembl_gene_id":"ENSG00000202339.1","gene_symbol":"RNU4-45P","gene_name":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481186","summary":null,"start":22205192,"end":22205332,"strand":1,"description":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]"}, {"versioned_ensembl_gene_id":"ENSG00000275901.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":16187313,"end":16187566,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202000.1","gene_symbol":"RNU1-36P","gene_name":"RNA, U1 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48378]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481783","summary":null,"start":88000237,"end":88000401,"strand":1,"description":"RNA, U1 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48378]"}, {"versioned_ensembl_gene_id":"ENSG00000201388.1","gene_symbol":"SNORA68B","gene_name":"small nucleolar RNA, H/ACA box 68B [Source:HGNC Symbol;Acc:HGNC:52213]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616972","summary":null,"start":32608337,"end":32608469,"strand":-1,"description":"small nucleolar RNA, H/ACA box 68B [Source:HGNC Symbol;Acc:HGNC:52213]"}, {"versioned_ensembl_gene_id":"ENSG00000201642.1","gene_symbol":"RNU6-865P","gene_name":"RNA, U6 small nuclear 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:47828]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479948","summary":null,"start":100952627,"end":100952733,"strand":1,"description":"RNA, U6 small nuclear 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:47828]"}, {"versioned_ensembl_gene_id":"ENSG00000207811.3","gene_symbol":"MIR34B","gene_name":"microRNA 34b [Source:HGNC Symbol;Acc:HGNC:31636]","synonyms":"MIRN34B,hsa-mir-34b","biotype":"miRNA","ncbi_id":"407041","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111512938,"end":111513021,"strand":1,"description":"microRNA 34b [Source:HGNC Symbol;Acc:HGNC:31636]"}, {"versioned_ensembl_gene_id":"ENSG00000207759.1","gene_symbol":"MIR181A1","gene_name":"microRNA 181a-1 [Source:HGNC Symbol;Acc:HGNC:31590]","synonyms":"MIRN213,MIRN181A1,hsa-mir-213","biotype":"miRNA","ncbi_id":"406995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":198859044,"end":198859153,"strand":-1,"description":"microRNA 181a-1 [Source:HGNC Symbol;Acc:HGNC:31590]"}, {"versioned_ensembl_gene_id":"ENSG00000201770.1","gene_symbol":"RNU6-384P","gene_name":"RNA, U6 small nuclear 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:47347]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481299","summary":null,"start":31581089,"end":31581192,"strand":1,"description":"RNA, U6 small nuclear 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:47347]"}, {"versioned_ensembl_gene_id":"ENSG00000252988.1","gene_symbol":"RNU6-111P","gene_name":"RNA, U6 small nuclear 111, pseudogene [Source:HGNC Symbol;Acc:HGNC:47074]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481212","summary":null,"start":73298683,"end":73298787,"strand":1,"description":"RNA, U6 small nuclear 111, pseudogene [Source:HGNC Symbol;Acc:HGNC:47074]"}, {"versioned_ensembl_gene_id":"ENSG00000264419.1","gene_symbol":"MIR548AC","gene_name":"microRNA 548ac [Source:HGNC Symbol;Acc:HGNC:41626]","synonyms":"hsa-mir-548ac","biotype":"miRNA","ncbi_id":"100616384","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116560024,"end":116560111,"strand":-1,"description":"microRNA 548ac [Source:HGNC Symbol;Acc:HGNC:41626]"}, {"versioned_ensembl_gene_id":"ENSG00000212316.1","gene_symbol":"RNU6-1228P","gene_name":"RNA, U6 small nuclear 1228, pseudogene [Source:HGNC Symbol;Acc:HGNC:48191]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480103","summary":null,"start":75198071,"end":75198177,"strand":1,"description":"RNA, U6 small nuclear 1228, pseudogene [Source:HGNC Symbol;Acc:HGNC:48191]"}, {"versioned_ensembl_gene_id":"ENSG00000266263.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30908902,"end":30909204,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000200799.1","gene_symbol":"RNU6-770P","gene_name":"RNA, U6 small nuclear 770, pseudogene [Source:HGNC Symbol;Acc:HGNC:47733]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481423","summary":null,"start":108392073,"end":108392177,"strand":1,"description":"RNA, U6 small nuclear 770, pseudogene [Source:HGNC Symbol;Acc:HGNC:47733]"}, {"versioned_ensembl_gene_id":"ENSG00000277605.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47476822,"end":47477152,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000273875.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000239128.1","gene_symbol":"SNORD13P3","gene_name":"small nucleolar RNA, C/D box 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10112]","synonyms":"U13.4B,U13,RNU13P3","biotype":"snoRNA","ncbi_id":"6078","summary":null,"start":47250523,"end":47250626,"strand":-1,"description":"small nucleolar RNA, C/D box 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10112]"}, {"versioned_ensembl_gene_id":"ENSG00000200225.1","gene_symbol":"RNA5SP382","gene_name":"RNA, 5S ribosomal pseudogene 382 [Source:HGNC Symbol;Acc:HGNC:43282]","synonyms":"RN5S382","biotype":"rRNA","ncbi_id":"100873637","summary":null,"start":20414987,"end":20415098,"strand":1,"description":"RNA, 5S ribosomal pseudogene 382 [Source:HGNC Symbol;Acc:HGNC:43282]"}, {"versioned_ensembl_gene_id":"ENSG00000201201.1","gene_symbol":"RN7SKP118","gene_name":"RNA, 7SK small nuclear pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:45842]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106633802","summary":null,"start":67321658,"end":67321987,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:45842]"}, {"versioned_ensembl_gene_id":"ENSG00000222356.1","gene_symbol":"RNU6-710P","gene_name":"RNA, U6 small nuclear 710, pseudogene [Source:HGNC Symbol;Acc:HGNC:47673]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479880","summary":null,"start":111996635,"end":111996739,"strand":-1,"description":"RNA, U6 small nuclear 710, pseudogene [Source:HGNC Symbol;Acc:HGNC:47673]"}, {"versioned_ensembl_gene_id":"ENSG00000200942.1","gene_symbol":"RNU6-501P","gene_name":"RNA, U6 small nuclear 501, pseudogene [Source:HGNC Symbol;Acc:HGNC:47464]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481339","summary":null,"start":201733406,"end":201733505,"strand":1,"description":"RNA, U6 small nuclear 501, pseudogene [Source:HGNC Symbol;Acc:HGNC:47464]"}, {"versioned_ensembl_gene_id":"ENSG00000278264.1","gene_symbol":"MIR6803","gene_name":"microRNA 6803 [Source:HGNC Symbol;Acc:HGNC:50035]","synonyms":"hsa-mir-6803","biotype":"miRNA","ncbi_id":"102466739","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55245186,"end":55245250,"strand":-1,"description":"microRNA 6803 [Source:HGNC Symbol;Acc:HGNC:50035]"}, {"versioned_ensembl_gene_id":"ENSG00000200257.1","gene_symbol":"RNU6-97P","gene_name":"RNA, U6 small nuclear 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:47060]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480551","summary":null,"start":76752912,"end":76753015,"strand":1,"description":"RNA, U6 small nuclear 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:47060]"}, {"versioned_ensembl_gene_id":"ENSG00000277595.1","gene_symbol":"AC007546.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":110032245,"end":110032803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255348.1","gene_symbol":"AP001775.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134178824,"end":134186166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284542.1","gene_symbol":"MIR3614","gene_name":"microRNA 3614 [Source:HGNC Symbol;Acc:HGNC:38995]","synonyms":"hsa-mir-3614","biotype":"miRNA","ncbi_id":"100500827","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56891270,"end":56891355,"strand":-1,"description":"microRNA 3614 [Source:HGNC Symbol;Acc:HGNC:38995]"}, {"versioned_ensembl_gene_id":"ENSG00000281557.1","gene_symbol":"AL357055.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113013524,"end":113074942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283416.1","gene_symbol":"MIR1910","gene_name":"microRNA 1910 [Source:HGNC Symbol;Acc:HGNC:35394]","synonyms":"MIRN1910,hsa-mir-1910","biotype":"miRNA","ncbi_id":"100302261","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85741621,"end":85741700,"strand":-1,"description":"microRNA 1910 [Source:HGNC Symbol;Acc:HGNC:35394]"}, {"versioned_ensembl_gene_id":"ENSG00000251814.1","gene_symbol":"RN7SKP18","gene_name":"RNA, 7SK small nuclear pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:45742]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480838","summary":null,"start":117299364,"end":117299638,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:45742]"}, {"versioned_ensembl_gene_id":"ENSG00000265855.1","gene_symbol":"MIR4514","gene_name":"microRNA 4514 [Source:HGNC Symbol;Acc:HGNC:41845]","synonyms":"hsa-mir-4514","biotype":"miRNA","ncbi_id":"100616181","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80997417,"end":80997473,"strand":-1,"description":"microRNA 4514 [Source:HGNC Symbol;Acc:HGNC:41845]"}, {"versioned_ensembl_gene_id":"ENSG00000244404.3","gene_symbol":"RN7SL216P","gene_name":"RNA, 7SL, cytoplasmic 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:46232]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480495","summary":null,"start":25020166,"end":25020463,"strand":-1,"description":"RNA, 7SL, cytoplasmic 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:46232]"}, {"versioned_ensembl_gene_id":"ENSG00000207961.3","gene_symbol":"MIR496","gene_name":"microRNA 496 [Source:HGNC Symbol;Acc:HGNC:32086]","synonyms":"MIRN496,hsa-mir-496","biotype":"miRNA","ncbi_id":"574454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101060573,"end":101060674,"strand":1,"description":"microRNA 496 [Source:HGNC Symbol;Acc:HGNC:32086]"}, {"versioned_ensembl_gene_id":"ENSG00000266611.1","gene_symbol":"MIR4703","gene_name":"microRNA 4703 [Source:HGNC Symbol;Acc:HGNC:41817]","synonyms":"hsa-mir-4703","biotype":"miRNA","ncbi_id":"100616423","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51552589,"end":51552667,"strand":1,"description":"microRNA 4703 [Source:HGNC Symbol;Acc:HGNC:41817]"}, {"versioned_ensembl_gene_id":"ENSG00000266188.1","gene_symbol":"MIR5095","gene_name":"microRNA 5095 [Source:HGNC Symbol;Acc:HGNC:41849]","synonyms":"hsa-mir-5095","biotype":"miRNA","ncbi_id":"100616458","summary":"This record was withdrawn by miRBase.","start":52934930,"end":52935017,"strand":1,"description":"microRNA 5095 [Source:HGNC Symbol;Acc:HGNC:41849]"}, {"versioned_ensembl_gene_id":"ENSG00000200726.1","gene_symbol":"SNORD115-8","gene_name":"small nucleolar RNA, C/D box 115-8 [Source:HGNC Symbol;Acc:HGNC:33027]","synonyms":"HBII-52-8","biotype":"snoRNA","ncbi_id":"100033445","summary":null,"start":25184306,"end":25184387,"strand":1,"description":"small nucleolar RNA, C/D box 115-8 [Source:HGNC Symbol;Acc:HGNC:33027]"}, {"versioned_ensembl_gene_id":"ENSG00000202184.1","gene_symbol":"RNU6-1283P","gene_name":"RNA, U6 small nuclear 1283, pseudogene [Source:HGNC Symbol;Acc:HGNC:48246]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481782","summary":null,"start":246189014,"end":246189118,"strand":-1,"description":"RNA, U6 small nuclear 1283, pseudogene [Source:HGNC Symbol;Acc:HGNC:48246]"}, {"versioned_ensembl_gene_id":"ENSG00000252061.1","gene_symbol":"RNU6-415P","gene_name":"RNA, U6 small nuclear 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:47378]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481309","summary":null,"start":78898840,"end":78898936,"strand":-1,"description":"RNA, U6 small nuclear 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:47378]"}, {"versioned_ensembl_gene_id":"ENSG00000273537.1","gene_symbol":"ZEB2_AS1_3","gene_name":"ZEB2 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF01986]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144520456,"end":144520555,"strand":1,"description":"ZEB2 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF01986]"}, {"versioned_ensembl_gene_id":"ENSG00000201403.1","gene_symbol":"SNORD14B","gene_name":"small nucleolar RNA, C/D box 14B [Source:HGNC Symbol;Acc:HGNC:31803]","synonyms":"U14B,U14,RNU14B","biotype":"snoRNA","ncbi_id":"85388","summary":null,"start":17075779,"end":17075868,"strand":-1,"description":"small nucleolar RNA, C/D box 14B [Source:HGNC Symbol;Acc:HGNC:31803]"}, {"versioned_ensembl_gene_id":"ENSG00000251185.1","gene_symbol":"AC025244.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75269068,"end":75361182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278073.1","gene_symbol":"MIR6726","gene_name":"microRNA 6726 [Source:HGNC Symbol;Acc:HGNC:50009]","synonyms":"hsa-mir-6726","biotype":"miRNA","ncbi_id":"102465434","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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[provided by RefSeq, Sep 2009]","start":118974586,"end":118974670,"strand":1,"description":"microRNA 1244-2 [Source:HGNC Symbol;Acc:HGNC:38321]"}, {"versioned_ensembl_gene_id":"ENSG00000252097.1","gene_symbol":"RNU6-346P","gene_name":"RNA, U6 small nuclear 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:47309]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481768","summary":null,"start":76800664,"end":76800774,"strand":-1,"description":"RNA, U6 small nuclear 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:47309]"}, {"versioned_ensembl_gene_id":"ENSG00000202469.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10061222,"end":10061323,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252390.1","gene_symbol":"RNU5F-4P","gene_name":"RNA, U5F small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42516]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873867","summary":null,"start":31594093,"end":31594206,"strand":-1,"description":"RNA, U5F small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42516]"}, {"versioned_ensembl_gene_id":"ENSG00000272166.1","gene_symbol":"SNORD5","gene_name":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]","synonyms":"mgh28S-2410","biotype":"snoRNA","ncbi_id":"692072","summary":null,"start":25555543,"end":25555606,"strand":-1,"description":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]"}, {"versioned_ensembl_gene_id":"ENSG00000207408.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53324562,"end":53324674,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274713.1","gene_symbol":"MIR7974","gene_name":"microRNA 7974 [Source:HGNC Symbol;Acc:HGNC:49992]","synonyms":"hsa-mir-7974","biotype":"miRNA","ncbi_id":"102465856","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. 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[provided by RefSeq, Sep 2009]","start":11495544,"end":11495622,"strand":-1,"description":"microRNA 7974 [Source:HGNC Symbol;Acc:HGNC:49992]"}, {"versioned_ensembl_gene_id":"ENSG00000252132.1","gene_symbol":"RNU6-795P","gene_name":"RNA, U6 small nuclear 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:47758]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480610","summary":null,"start":38043873,"end":38043975,"strand":-1,"description":"RNA, U6 small nuclear 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:47758]"}, {"versioned_ensembl_gene_id":"ENSG00000200895.1","gene_symbol":"RN7SKP245","gene_name":"RNA, 7SK small nuclear pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:45969]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480909","summary":null,"start":131820334,"end":131820653,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:45969]"}, {"versioned_ensembl_gene_id":"ENSG00000275391.1","gene_symbol":"MIR6770-3","gene_name":"microRNA 6770-3 [Source:HGNC Symbol;Acc:HGNC:50034]","synonyms":"hsa-mir-6770-3","biotype":"miRNA","ncbi_id":"102466259","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18379351,"end":18379410,"strand":-1,"description":"microRNA 6770-3 [Source:HGNC Symbol;Acc:HGNC:50034]"}, {"versioned_ensembl_gene_id":"ENSG00000238326.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56000518,"end":56000621,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000276941.1","gene_symbol":"MIR4509-1","gene_name":"microRNA 4509-1 [Source:HGNC Symbol;Acc:HGNC:41860]","synonyms":"hsa-mir-4509-1","biotype":"miRNA","ncbi_id":"100616223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23197827,"end":23197920,"strand":1,"description":"microRNA 4509-1 [Source:HGNC Symbol;Acc:HGNC:41860]"}, {"versioned_ensembl_gene_id":"ENSG00000200635.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55582733,"end":55582834,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266704.1","gene_symbol":"MIR4498","gene_name":"microRNA 4498 [Source:HGNC Symbol;Acc:HGNC:41838]","synonyms":"hsa-mir-4498","biotype":"miRNA","ncbi_id":"100616179","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120155434,"end":120155499,"strand":-1,"description":"microRNA 4498 [Source:HGNC Symbol;Acc:HGNC:41838]"}, {"versioned_ensembl_gene_id":"ENSG00000252073.1","gene_symbol":"RNU6-947P","gene_name":"RNA, U6 small nuclear 947, pseudogene [Source:HGNC Symbol;Acc:HGNC:47910]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479985","summary":null,"start":244954858,"end":244954963,"strand":1,"description":"RNA, U6 small nuclear 947, pseudogene [Source:HGNC Symbol;Acc:HGNC:47910]"}, {"versioned_ensembl_gene_id":"ENSG00000265355.1","gene_symbol":"MIR3136","gene_name":"microRNA 3136 [Source:HGNC Symbol;Acc:HGNC:38340]","synonyms":"hsa-mir-3136","biotype":"miRNA","ncbi_id":"100422859","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69048958,"end":69049035,"strand":-1,"description":"microRNA 3136 [Source:HGNC Symbol;Acc:HGNC:38340]"}, {"versioned_ensembl_gene_id":"ENSG00000252292.1","gene_symbol":"RN7SKP238","gene_name":"RNA, 7SK small nuclear pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:45962]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479201","summary":null,"start":85650012,"end":85650260,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:45962]"}, {"versioned_ensembl_gene_id":"ENSG00000221114.1","gene_symbol":"RNU6ATAC30P","gene_name":"RNA, U6atac small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46929]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481868","summary":null,"start":49684544,"end":49684665,"strand":1,"description":"RNA, U6atac small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46929]"}, {"versioned_ensembl_gene_id":"ENSG00000273648.1","gene_symbol":"MIR8065","gene_name":"microRNA 8065 [Source:HGNC Symbol;Acc:HGNC:49959]","synonyms":"hsa-mir-8065","biotype":"miRNA","ncbi_id":"102465867","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5632467,"end":5632566,"strand":1,"description":"microRNA 8065 [Source:HGNC Symbol;Acc:HGNC:49959]"}, {"versioned_ensembl_gene_id":"ENSG00000201492.1","gene_symbol":"RNA5SP78","gene_name":"RNA, 5S ribosomal pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:42855]","synonyms":"RN5S78","biotype":"rRNA","ncbi_id":"100873312","summary":null,"start":229549905,"end":229550022,"strand":1,"description":"RNA, 5S ribosomal pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:42855]"}, {"versioned_ensembl_gene_id":"ENSG00000284160.1","gene_symbol":"MIR7706","gene_name":"microRNA 7706 [Source:HGNC Symbol;Acc:HGNC:50110]","synonyms":"hsa-mir-7706","biotype":"miRNA","ncbi_id":"102465803","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85380596,"end":85380662,"strand":1,"description":"microRNA 7706 [Source:HGNC Symbol;Acc:HGNC:50110]"}, {"versioned_ensembl_gene_id":"ENSG00000275372.1","gene_symbol":"ZEB2_AS1_1","gene_name":"ZEB2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF01984]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144518447,"end":144518574,"strand":1,"description":"ZEB2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF01984]"}, {"versioned_ensembl_gene_id":"ENSG00000239105.1","gene_symbol":"RNU7-73P","gene_name":"RNA, U7 small nuclear 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:34169]","synonyms":"U7.73","biotype":"snRNA","ncbi_id":"100151670","summary":null,"start":37573151,"end":37573213,"strand":-1,"description":"RNA, U7 small nuclear 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:34169]"}, {"versioned_ensembl_gene_id":"ENSG00000200914.1","gene_symbol":"RNA5SP435","gene_name":"RNA, 5S ribosomal pseudogene 435 [Source:HGNC Symbol;Acc:HGNC:43335]","synonyms":"RN5S435","biotype":"rRNA","ncbi_id":"106479013","summary":null,"start":6600944,"end":6601051,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 435 [Source:HGNC Symbol;Acc:HGNC:43335]"}, {"versioned_ensembl_gene_id":"ENSG00000239002.3","gene_symbol":"SCARNA10","gene_name":"small Cajal body-specific RNA 10 [Source:HGNC Symbol;Acc:HGNC:32567]","synonyms":"U85","biotype":"snoRNA","ncbi_id":"692148","summary":null,"start":6510222,"end":6510551,"strand":1,"description":"small Cajal body-specific RNA 10 [Source:HGNC Symbol;Acc:HGNC:32567]"}, {"versioned_ensembl_gene_id":"ENSG00000267421.6","gene_symbol":"AC005498.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56536156,"end":56538575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212040.3","gene_symbol":"MIR543","gene_name":"microRNA 543 [Source:HGNC Symbol;Acc:HGNC:33664]","synonyms":"MIRN543,hsa-mir-543","biotype":"miRNA","ncbi_id":"100126335","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101031987,"end":101032064,"strand":1,"description":"microRNA 543 [Source:HGNC Symbol;Acc:HGNC:33664]"}, {"versioned_ensembl_gene_id":"ENSG00000216192.1","gene_symbol":"MIR920","gene_name":"microRNA 920 [Source:HGNC Symbol;Acc:HGNC:33670]","synonyms":"hsa-mir-920,MIRN920","biotype":"miRNA","ncbi_id":"100126320","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24212421,"end":24212495,"strand":1,"description":"microRNA 920 [Source:HGNC Symbol;Acc:HGNC:33670]"}, {"versioned_ensembl_gene_id":"ENSG00000278359.1","gene_symbol":"MIR7155","gene_name":"microRNA 7155 [Source:HGNC Symbol;Acc:HGNC:50005]","synonyms":"hsa-mir-7155","biotype":"miRNA","ncbi_id":"102466815","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64341849,"end":64341904,"strand":-1,"description":"microRNA 7155 [Source:HGNC Symbol;Acc:HGNC:50005]"}, {"versioned_ensembl_gene_id":"ENSG00000240014.3","gene_symbol":"RN7SL254P","gene_name":"RNA, 7SL, cytoplasmic 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:46270]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480991","summary":null,"start":147808926,"end":147809209,"strand":1,"description":"RNA, 7SL, cytoplasmic 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:46270]"}, {"versioned_ensembl_gene_id":"ENSG00000207874.1","gene_symbol":"MIR610","gene_name":"microRNA 610 [Source:HGNC Symbol;Acc:HGNC:32866]","synonyms":"MIRN610,hsa-mir-610","biotype":"miRNA","ncbi_id":"693195","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28056815,"end":28056910,"strand":1,"description":"microRNA 610 [Source:HGNC Symbol;Acc:HGNC:32866]"}, {"versioned_ensembl_gene_id":"ENSG00000200686.1","gene_symbol":"RNY3P3","gene_name":"RNA, Ro-associated Y3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42487]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862669","summary":null,"start":78355227,"end":78355328,"strand":-1,"description":"RNA, Ro-associated Y3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42487]"}, {"versioned_ensembl_gene_id":"ENSG00000281894.2","gene_symbol":"ZKSCAN7","gene_name":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]","synonyms":"ZSCAN39,ZNF64,ZNF448,ZNF167,FLJ12738","biotype":"protein_coding","ncbi_id":"55888","summary":null,"start":44555193,"end":44594173,"strand":1,"description":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]"}, {"versioned_ensembl_gene_id":"ENSG00000222585.1","gene_symbol":"RNA5SP494","gene_name":"RNA, 5S ribosomal pseudogene 494 [Source:HGNC Symbol;Acc:HGNC:43394]","synonyms":"RN5S494","biotype":"rRNA","ncbi_id":"100873736","summary":null,"start":25715041,"end":25715169,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 494 [Source:HGNC Symbol;Acc:HGNC:43394]"}, {"versioned_ensembl_gene_id":"ENSG00000238490.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108060818,"end":108060930,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201715.1","gene_symbol":"RN7SKP133","gene_name":"RNA, 7SK small nuclear pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:45857]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481812","summary":null,"start":17345616,"end":17345955,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:45857]"}, {"versioned_ensembl_gene_id":"ENSG00000263595.2","gene_symbol":"RN7SL823P","gene_name":"RNA, 7SL, cytoplasmic 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:46839]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479522","summary":null,"start":16910490,"end":16910784,"strand":-1,"description":"RNA, 7SL, cytoplasmic 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:46839]"}, {"versioned_ensembl_gene_id":"ENSG00000283204.1","gene_symbol":"MIR4434","gene_name":"microRNA 4434 [Source:HGNC Symbol;Acc:HGNC:41832]","synonyms":"hsa-mir-4434","biotype":"miRNA","ncbi_id":"100616419","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64525513,"end":64525565,"strand":1,"description":"microRNA 4434 [Source:HGNC Symbol;Acc:HGNC:41832]"}, {"versioned_ensembl_gene_id":"ENSG00000201810.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":180542701,"end":180542836,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000238819.1","gene_symbol":"SNORD11","gene_name":"Small nucleolar RNA SNORD11 [Source:RFAM;Acc:RF01182]","synonyms":"HBII-95","biotype":"snoRNA","ncbi_id":"692058","summary":null,"start":46351662,"end":46351746,"strand":-1,"description":"Small nucleolar RNA SNORD11 [Source:RFAM;Acc:RF01182]"}, {"versioned_ensembl_gene_id":"ENSG00000280683.1","gene_symbol":"AL354704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30388935,"end":30575012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263752.1","gene_symbol":"MIR3133","gene_name":"microRNA 3133 [Source:HGNC Symbol;Acc:HGNC:38305]","synonyms":"hsa-mir-3133","biotype":"miRNA","ncbi_id":"100422942","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":241477905,"end":241477982,"strand":1,"description":"microRNA 3133 [Source:HGNC Symbol;Acc:HGNC:38305]"}, {"versioned_ensembl_gene_id":"ENSG00000266180.1","gene_symbol":"MIR4282","gene_name":"microRNA 4282 [Source:HGNC Symbol;Acc:HGNC:38189]","synonyms":"hsa-mir-4282","biotype":"miRNA","ncbi_id":"100423005","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72967687,"end":72967753,"strand":-1,"description":"microRNA 4282 [Source:HGNC Symbol;Acc:HGNC:38189]"}, {"versioned_ensembl_gene_id":"ENSG00000201843.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133302470,"end":133302563,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240961.3","gene_symbol":"RN7SL415P","gene_name":"RNA, 7SL, cytoplasmic 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:46431]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479375","summary":null,"start":91739609,"end":91739897,"strand":1,"description":"RNA, 7SL, cytoplasmic 415, pseudogene [Source:HGNC Symbol;Acc:HGNC:46431]"}, {"versioned_ensembl_gene_id":"ENSG00000281226.2","gene_symbol":"AL590644.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17189783,"end":17197617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264834.1","gene_symbol":"MIR1273F","gene_name":"microRNA 1273f [Source:HGNC Symbol;Acc:HGNC:41733]","synonyms":"hsa-mir-1273f","biotype":"miRNA","ncbi_id":"100616156","summary":"This record was withdrawn by miRBase.","start":52928674,"end":52928772,"strand":1,"description":"microRNA 1273f [Source:HGNC Symbol;Acc:HGNC:41733]"}, {"versioned_ensembl_gene_id":"ENSG00000253057.1","gene_symbol":"RN7SKP57","gene_name":"RNA, 7SK small nuclear pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:45781]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479120","summary":null,"start":111719769,"end":111720061,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:45781]"}, {"versioned_ensembl_gene_id":"ENSG00000206915.1","gene_symbol":"RNU6-439P","gene_name":"RNA, U6 small nuclear 439, pseudogene [Source:HGNC Symbol;Acc:HGNC:47402]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481317","summary":null,"start":49233794,"end":49233899,"strand":-1,"description":"RNA, U6 small nuclear 439, pseudogene [Source:HGNC Symbol;Acc:HGNC:47402]"}, {"versioned_ensembl_gene_id":"ENSG00000276859.1","gene_symbol":"GNAS-AS1_1","gene_name":"GNAS antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02127]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58842030,"end":58842132,"strand":1,"description":"GNAS antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02127]"}, {"versioned_ensembl_gene_id":"ENSG00000239057.2","gene_symbol":"MIR500B","gene_name":"microRNA 500b [Source:HGNC Symbol;Acc:HGNC:38223]","synonyms":"hsa-mir-500b","biotype":"miRNA","ncbi_id":"100422911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50010672,"end":50010750,"strand":1,"description":"microRNA 500b [Source:HGNC Symbol;Acc:HGNC:38223]"}, {"versioned_ensembl_gene_id":"ENSG00000201263.1","gene_symbol":"SNORD114-6","gene_name":"small nucleolar RNA, C/D box 114-6 [Source:HGNC Symbol;Acc:HGNC:32994]","synonyms":"14q(II-6)","biotype":"snoRNA","ncbi_id":"767582","summary":null,"start":100957166,"end":100957237,"strand":1,"description":"small nucleolar RNA, C/D box 114-6 [Source:HGNC Symbol;Acc:HGNC:32994]"}, {"versioned_ensembl_gene_id":"ENSG00000207268.1","gene_symbol":"SNORA70C","gene_name":"small nucleolar RNA, H/ACA box 70C [Source:HGNC Symbol;Acc:HGNC:33619]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124538","summary":"This gene produces a small nucleolar RNA (snoRNA) that plays a role in post-transcriptional modification. This snoRNA is a type-3 retrotransposed snoRNA, where the ribosomal protein L10 gene on chromosome X is its parental gene, and this, together with part of the parental gene, was subsequently mobilized into an intron of the astrotactin 2 host gene on chromosome 9. This snoRNA contains a H/ACA box, which serves as a guide for the pseudouridylation of selected bases of ribosomal RNA by forming short duplexes with the 18S rRNA U1692, the target for this snoRNA. This gene is specific to human, chimp and orangutan, and is not found in the genomes of rhesus or marmoset. [provided by RefSeq, Jun 2010]","start":117181066,"end":117181200,"strand":-1,"description":"small nucleolar RNA, H/ACA box 70C [Source:HGNC Symbol;Acc:HGNC:33619]"}, {"versioned_ensembl_gene_id":"ENSG00000280781.1","gene_symbol":"EI24P3","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131881","summary":null,"start":44524744,"end":44525805,"strand":-1,"description":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]"}, {"versioned_ensembl_gene_id":"ENSG00000238386.1","gene_symbol":"RNU7-48P","gene_name":"RNA, U7 small nuclear 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:34144]","synonyms":"U7.48","biotype":"snRNA","ncbi_id":"100147835","summary":null,"start":70513294,"end":70513356,"strand":1,"description":"RNA, U7 small nuclear 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:34144]"}, {"versioned_ensembl_gene_id":"ENSG00000201026.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2184710,"end":2184820,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238923.1","gene_symbol":"RNU7-1","gene_name":"RNA, U7 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:34033]","synonyms":"U7.1,RNU7","biotype":"snRNA","ncbi_id":"100147744","summary":null,"start":6943816,"end":6943878,"strand":1,"description":"RNA, U7 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:34033]"}, {"versioned_ensembl_gene_id":"ENSG00000278331.1","gene_symbol":"RNU6-156P","gene_name":"RNA, U6 small nuclear 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:47119]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479635","summary":null,"start":40759600,"end":40759706,"strand":-1,"description":"RNA, U6 small nuclear 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:47119]"}, {"versioned_ensembl_gene_id":"ENSG00000252037.1","gene_symbol":"RNU6-162P","gene_name":"RNA, U6 small nuclear 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:47125]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481226","summary":null,"start":143574746,"end":143574848,"strand":1,"description":"RNA, U6 small nuclear 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:47125]"}, {"versioned_ensembl_gene_id":"ENSG00000274210.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":148522601,"end":148522765,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000252205.1","gene_symbol":"RNU6-764P","gene_name":"RNA, U6 small nuclear 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:47727]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479904","summary":null,"start":152250572,"end":152250676,"strand":-1,"description":"RNA, U6 small nuclear 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:47727]"}, {"versioned_ensembl_gene_id":"ENSG00000278998.1","gene_symbol":"AC099552.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":155222903,"end":155223851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207976.1","gene_symbol":"MIR607","gene_name":"microRNA 607 [Source:HGNC Symbol;Acc:HGNC:32863]","synonyms":"hsa-mir-607,MIRN607","biotype":"miRNA","ncbi_id":"693192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96828669,"end":96828764,"strand":-1,"description":"microRNA 607 [Source:HGNC Symbol;Acc:HGNC:32863]"}, {"versioned_ensembl_gene_id":"ENSG00000284587.1","gene_symbol":"MIR943","gene_name":"microRNA 943 [Source:HGNC Symbol;Acc:HGNC:33689]","synonyms":"MIRN943,hsa-mir-943","biotype":"miRNA","ncbi_id":"100126332","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1986384,"end":1986477,"strand":-1,"description":"microRNA 943 [Source:HGNC Symbol;Acc:HGNC:33689]"}, {"versioned_ensembl_gene_id":"ENSG00000283634.1","gene_symbol":"MIR3155B","gene_name":"microRNA 3155b [Source:HGNC Symbol;Acc:HGNC:50003]","synonyms":"hsa-mir-3155b","biotype":"miRNA","ncbi_id":"100628560","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6152207,"end":6152262,"strand":-1,"description":"microRNA 3155b [Source:HGNC Symbol;Acc:HGNC:50003]"}, {"versioned_ensembl_gene_id":"ENSG00000264984.1","gene_symbol":"MIR5691","gene_name":"microRNA 5691 [Source:HGNC Symbol;Acc:HGNC:43545]","synonyms":"hsa-mir-5691","biotype":"miRNA","ncbi_id":"100847015","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9090312,"end":9090379,"strand":-1,"description":"microRNA 5691 [Source:HGNC Symbol;Acc:HGNC:43545]"}, {"versioned_ensembl_gene_id":"ENSG00000199038.1","gene_symbol":"MIR210","gene_name":"microRNA 210 [Source:HGNC Symbol;Acc:HGNC:31587]","synonyms":"hsa-mir-210,MIRN210","biotype":"miRNA","ncbi_id":"406992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":568089,"end":568198,"strand":-1,"description":"microRNA 210 [Source:HGNC Symbol;Acc:HGNC:31587]"}, {"versioned_ensembl_gene_id":"ENSG00000251825.1","gene_symbol":"RN7SKP19","gene_name":"RNA, 7SK small nuclear pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:45743]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479103","summary":null,"start":73191604,"end":73191855,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:45743]"}, {"versioned_ensembl_gene_id":"ENSG00000264192.1","gene_symbol":"RN7SL117P","gene_name":"RNA, 7SL, cytoplasmic 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:46133]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479264","summary":null,"start":21922993,"end":21923288,"strand":1,"description":"RNA, 7SL, cytoplasmic 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:46133]"}, {"versioned_ensembl_gene_id":"ENSG00000207728.1","gene_symbol":"MIR449B","gene_name":"microRNA 449b [Source:HGNC Symbol;Acc:HGNC:32794]","synonyms":"MIRN449B,hsa-mir-449b","biotype":"miRNA","ncbi_id":"693123","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55170646,"end":55170742,"strand":-1,"description":"microRNA 449b [Source:HGNC Symbol;Acc:HGNC:32794]"}, {"versioned_ensembl_gene_id":"ENSG00000239542.3","gene_symbol":"RN7SL399P","gene_name":"RNA, 7SL, cytoplasmic 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:46415]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479370","summary":null,"start":41730127,"end":41730405,"strand":-1,"description":"RNA, 7SL, cytoplasmic 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:46415]"}, {"versioned_ensembl_gene_id":"ENSG00000276669.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86216596,"end":86216878,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000264141.1","gene_symbol":"MIR3928","gene_name":"microRNA 3928 [Source:HGNC Symbol;Acc:HGNC:38933]","synonyms":"hsa-mir-3928","biotype":"miRNA","ncbi_id":"100500901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31160062,"end":31160119,"strand":-1,"description":"microRNA 3928 [Source:HGNC Symbol;Acc:HGNC:38933]"}, {"versioned_ensembl_gene_id":"ENSG00000207098.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":32841861,"end":32841995,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000206622.1","gene_symbol":"SNORA69","gene_name":"small nucleolar RNA, H/ACA box 69 [Source:HGNC Symbol;Acc:HGNC:10226]","synonyms":"U69,RNU69","biotype":"snoRNA","ncbi_id":"26779","summary":"This gene encodes a member of the family of box ACA small nucleolar RNAs, characterized by a consensus ACA motif positioned 3 nucleotides from the 3' end of the RNAs and a double-hairpin structure. The box ACA small nucleolar RNAs may play a role in rRNA maturation. This gene is co-transcribed with the ribosomal protein L39 gene. [provided by RefSeq, Oct 2009]","start":119787353,"end":119787484,"strand":-1,"description":"small nucleolar RNA, H/ACA box 69 [Source:HGNC Symbol;Acc:HGNC:10226]"}, {"versioned_ensembl_gene_id":"ENSG00000263815.2","gene_symbol":"RN7SL426P","gene_name":"RNA, 7SL, cytoplasmic 426, pseudogene [Source:HGNC Symbol;Acc:HGNC:46442]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481842","summary":null,"start":21229334,"end":21229628,"strand":-1,"description":"RNA, 7SL, cytoplasmic 426, pseudogene [Source:HGNC Symbol;Acc:HGNC:46442]"}, {"versioned_ensembl_gene_id":"ENSG00000252217.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65502741,"end":65502836,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211578.3","gene_symbol":"MIR766","gene_name":"microRNA 766 [Source:HGNC Symbol;Acc:HGNC:33139]","synonyms":"MIRN766,hsa-mir-766","biotype":"miRNA","ncbi_id":"768218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119646738,"end":119646848,"strand":-1,"description":"microRNA 766 [Source:HGNC Symbol;Acc:HGNC:33139]"}, {"versioned_ensembl_gene_id":"ENSG00000207782.3","gene_symbol":"MIR150","gene_name":"microRNA 150 [Source:HGNC Symbol;Acc:HGNC:31537]","synonyms":"hsa-mir-150,MIRN150","biotype":"miRNA","ncbi_id":"406942","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49500785,"end":49500868,"strand":-1,"description":"microRNA 150 [Source:HGNC Symbol;Acc:HGNC:31537]"}, {"versioned_ensembl_gene_id":"ENSG00000207736.1","gene_symbol":"MIR657","gene_name":"microRNA 657 [Source:HGNC Symbol;Acc:HGNC:32913]","synonyms":"MIRN657,hsa-mir-657","biotype":"miRNA","ncbi_id":"724027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81125276,"end":81125373,"strand":-1,"description":"microRNA 657 [Source:HGNC Symbol;Acc:HGNC:32913]"}, {"versioned_ensembl_gene_id":"ENSG00000199295.1","gene_symbol":"RNU6-1312P","gene_name":"RNA, U6 small nuclear 1312, pseudogene [Source:HGNC Symbol;Acc:HGNC:48275]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481594","summary":null,"start":83657735,"end":83657842,"strand":1,"description":"RNA, U6 small nuclear 1312, pseudogene [Source:HGNC Symbol;Acc:HGNC:48275]"}, {"versioned_ensembl_gene_id":"ENSG00000277478.1","gene_symbol":"MIR6165","gene_name":"microRNA 6165 [Source:HGNC Symbol;Acc:HGNC:50197]","synonyms":"hsa-mir-6165","biotype":"miRNA","ncbi_id":"102465141","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49510817,"end":49510900,"strand":1,"description":"microRNA 6165 [Source:HGNC Symbol;Acc:HGNC:50197]"}, {"versioned_ensembl_gene_id":"ENSG00000238759.1","gene_symbol":"RNU7-155P","gene_name":"RNA, U7 small nuclear 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:45689]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480825","summary":null,"start":71298156,"end":71298218,"strand":-1,"description":"RNA, U7 small nuclear 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:45689]"}, {"versioned_ensembl_gene_id":"ENSG00000201957.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":179169083,"end":179169210,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000202331.1","gene_symbol":"RNA5SP167","gene_name":"RNA, 5S ribosomal pseudogene 167 [Source:HGNC Symbol;Acc:HGNC:43067]","synonyms":"RN5S167","biotype":"rRNA","ncbi_id":"100873432","summary":null,"start":149907560,"end":149907675,"strand":1,"description":"RNA, 5S ribosomal pseudogene 167 [Source:HGNC Symbol;Acc:HGNC:43067]"}, {"versioned_ensembl_gene_id":"ENSG00000200832.1","gene_symbol":"SNORD114-4","gene_name":"small nucleolar RNA, C/D box 114-4 [Source:HGNC Symbol;Acc:HGNC:32992]","synonyms":"14q(II-4)","biotype":"snoRNA","ncbi_id":"767580","summary":null,"start":100954374,"end":100954448,"strand":1,"description":"small nucleolar RNA, C/D box 114-4 [Source:HGNC Symbol;Acc:HGNC:32992]"}, {"versioned_ensembl_gene_id":"ENSG00000199753.1","gene_symbol":"SNORD104","gene_name":"small nucleolar RNA, C/D box 104 [Source:HGNC Symbol;Acc:HGNC:32768]","synonyms":"U104","biotype":"snoRNA","ncbi_id":"692227","summary":null,"start":64146083,"end":64146152,"strand":1,"description":"small nucleolar RNA, C/D box 104 [Source:HGNC Symbol;Acc:HGNC:32768]"}, {"versioned_ensembl_gene_id":"ENSG00000200997.1","gene_symbol":"RNU1-85P","gene_name":"RNA, U1 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:48427]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480177","summary":null,"start":58679527,"end":58679690,"strand":-1,"description":"RNA, U1 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:48427]"}, {"versioned_ensembl_gene_id":"ENSG00000206636.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7976259,"end":7976360,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252550.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":105897523,"end":105897643,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000201023.1","gene_symbol":"RNY3P11","gene_name":"RNA, Ro-associated Y3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50887]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481713","summary":null,"start":109305494,"end":109305595,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50887]"}, {"versioned_ensembl_gene_id":"ENSG00000265176.1","gene_symbol":"MIR3202-1","gene_name":"microRNA 3202-1 [Source:HGNC Symbol;Acc:HGNC:38224]","synonyms":"hsa-mir-3202-1","biotype":"miRNA","ncbi_id":"100422987","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153981097,"end":153981177,"strand":1,"description":"microRNA 3202-1 [Source:HGNC Symbol;Acc:HGNC:38224]"}, {"versioned_ensembl_gene_id":"ENSG00000252539.1","gene_symbol":"RNA5SP462","gene_name":"RNA, 5S ribosomal pseudogene 462 [Source:HGNC Symbol;Acc:HGNC:43362]","synonyms":"RN5S462","biotype":"rRNA","ncbi_id":"100873706","summary":null,"start":453134,"end":453245,"strand":1,"description":"RNA, 5S ribosomal pseudogene 462 [Source:HGNC Symbol;Acc:HGNC:43362]"}, {"versioned_ensembl_gene_id":"ENSG00000208032.1","gene_symbol":"MIR548A3","gene_name":"microRNA 548a-3 [Source:HGNC Symbol;Acc:HGNC:32798]","synonyms":"MIRN548A3,hsa-mir-548a-3","biotype":"miRNA","ncbi_id":"693127","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104484369,"end":104484465,"strand":-1,"description":"microRNA 548a-3 [Source:HGNC Symbol;Acc:HGNC:32798]"}, {"versioned_ensembl_gene_id":"ENSG00000265226.1","gene_symbol":"MIR548AI","gene_name":"microRNA 548ai [Source:HGNC Symbol;Acc:HGNC:41854]","synonyms":"hsa-mir-548ai","biotype":"miRNA","ncbi_id":"100616347","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99124609,"end":99124696,"strand":1,"description":"microRNA 548ai [Source:HGNC Symbol;Acc:HGNC:41854]"}, {"versioned_ensembl_gene_id":"ENSG00000200241.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86159956,"end":86160066,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212389.1","gene_symbol":"RNU6-1275P","gene_name":"RNA, U6 small nuclear 1275, pseudogene [Source:HGNC Symbol;Acc:HGNC:48238]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480122","summary":null,"start":147877422,"end":147877528,"strand":1,"description":"RNA, U6 small nuclear 1275, pseudogene [Source:HGNC Symbol;Acc:HGNC:48238]"}, {"versioned_ensembl_gene_id":"ENSG00000283300.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28743208,"end":28743291,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277506.1","gene_symbol":"RN7SL802P","gene_name":"RNA, 7SL, cytoplasmic 802, pseudogene [Source:HGNC Symbol;Acc:HGNC:46818]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479513","summary":null,"start":101581830,"end":101582128,"strand":1,"description":"RNA, 7SL, cytoplasmic 802, pseudogene [Source:HGNC Symbol;Acc:HGNC:46818]"}, {"versioned_ensembl_gene_id":"ENSG00000241524.3","gene_symbol":"RN7SL632P","gene_name":"RNA, 7SL, cytoplasmic 632, pseudogene [Source:HGNC Symbol;Acc:HGNC:46648]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481095","summary":null,"start":60831664,"end":60831929,"strand":-1,"description":"RNA, 7SL, cytoplasmic 632, pseudogene [Source:HGNC Symbol;Acc:HGNC:46648]"}, {"versioned_ensembl_gene_id":"ENSG00000277553.1","gene_symbol":"HOTTIP_4","gene_name":"HOXA transcript at the distal tip, conserved region 4 [Source:RFAM;Acc:RF02043]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27206139,"end":27206303,"strand":1,"description":"HOXA transcript at the distal tip, conserved region 4 [Source:RFAM;Acc:RF02043]"}, {"versioned_ensembl_gene_id":"ENSG00000198982.4","gene_symbol":"MIR380","gene_name":"microRNA 380 [Source:HGNC Symbol;Acc:HGNC:31873]","synonyms":"MIRN380,hsa-mir-380","biotype":"miRNA","ncbi_id":"494329","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101025017,"end":101025077,"strand":1,"description":"microRNA 380 [Source:HGNC Symbol;Acc:HGNC:31873]"}, {"versioned_ensembl_gene_id":"ENSG00000206835.1","gene_symbol":"RNU1-74P","gene_name":"RNA, U1 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:48416]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480171","summary":null,"start":232832017,"end":232832187,"strand":-1,"description":"RNA, U1 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:48416]"}, {"versioned_ensembl_gene_id":"ENSG00000269889.1","gene_symbol":"AC078802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169769649,"end":169772043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282567.1","gene_symbol":"AC243913.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28716523,"end":28720895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277892.1","gene_symbol":"MIR6746","gene_name":"microRNA 6746 [Source:HGNC Symbol;Acc:HGNC:49925]","synonyms":"hsa-mir-6746","biotype":"miRNA","ncbi_id":"102465446","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61878216,"end":61878278,"strand":-1,"description":"microRNA 6746 [Source:HGNC Symbol;Acc:HGNC:49925]"}, {"versioned_ensembl_gene_id":"ENSG00000206766.1","gene_symbol":"RNU6-435P","gene_name":"RNA, U6 small nuclear 435, pseudogene [Source:HGNC Symbol;Acc:HGNC:47398]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479758","summary":null,"start":24218300,"end":24218404,"strand":1,"description":"RNA, U6 small nuclear 435, pseudogene [Source:HGNC Symbol;Acc:HGNC:47398]"}, {"versioned_ensembl_gene_id":"ENSG00000252766.1","gene_symbol":"RNU6-255P","gene_name":"RNA, U6 small nuclear 255, pseudogene [Source:HGNC Symbol;Acc:HGNC:47218]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481258","summary":null,"start":19018983,"end":19019087,"strand":-1,"description":"RNA, U6 small nuclear 255, pseudogene [Source:HGNC Symbol;Acc:HGNC:47218]"}, {"versioned_ensembl_gene_id":"ENSG00000274711.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130517049,"end":130517312,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000208036.1","gene_symbol":"MIR106B","gene_name":"microRNA 106b [Source:HGNC Symbol;Acc:HGNC:31495]","synonyms":"MIRN106B,hsa-mir-106b","biotype":"miRNA","ncbi_id":"406900","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100093993,"end":100094074,"strand":-1,"description":"microRNA 106b [Source:HGNC Symbol;Acc:HGNC:31495]"}, {"versioned_ensembl_gene_id":"ENSG00000264056.1","gene_symbol":"MIR5685","gene_name":"microRNA 5685 [Source:HGNC Symbol;Acc:HGNC:43543]","synonyms":"hsa-mir-5685","biotype":"miRNA","ncbi_id":"100847075","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53276993,"end":53277071,"strand":1,"description":"microRNA 5685 [Source:HGNC Symbol;Acc:HGNC:43543]"}, {"versioned_ensembl_gene_id":"ENSG00000201423.1","gene_symbol":"RN7SKP246","gene_name":"RNA, 7SK small nuclear pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:45970]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479204","summary":null,"start":144535354,"end":144535670,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:45970]"}, {"versioned_ensembl_gene_id":"ENSG00000206621.1","gene_symbol":"SNORD116-14","gene_name":"small nucleolar RNA, C/D box 116-14 [Source:HGNC Symbol;Acc:HGNC:33080]","synonyms":"HBII-85-14","biotype":"snoRNA","ncbi_id":"100033426","summary":null,"start":25080142,"end":25080233,"strand":1,"description":"small nucleolar RNA, C/D box 116-14 [Source:HGNC Symbol;Acc:HGNC:33080]"}, {"versioned_ensembl_gene_id":"ENSG00000264425.1","gene_symbol":"MIR4653","gene_name":"microRNA 4653 [Source:HGNC Symbol;Acc:HGNC:41562]","synonyms":"hsa-mir-4653","biotype":"miRNA","ncbi_id":"100616117","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101159473,"end":101159555,"strand":1,"description":"microRNA 4653 [Source:HGNC Symbol;Acc:HGNC:41562]"}, {"versioned_ensembl_gene_id":"ENSG00000265422.1","gene_symbol":"MIR4684","gene_name":"microRNA 4684 [Source:HGNC Symbol;Acc:HGNC:41695]","synonyms":"hsa-mir-4684","biotype":"miRNA","ncbi_id":"100616391","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22719517,"end":22719598,"strand":1,"description":"microRNA 4684 [Source:HGNC Symbol;Acc:HGNC:41695]"}, {"versioned_ensembl_gene_id":"ENSG00000283438.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23132730,"end":23133005,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253016.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38274448,"end":38274549,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200385.1","gene_symbol":"SNORA42","gene_name":"Small nucleolar RNA SNORA42/SNORA80 family [Source:RFAM;Acc:RF00406]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":37720425,"end":37720561,"strand":1,"description":"Small nucleolar RNA SNORA42/SNORA80 family [Source:RFAM;Acc:RF00406]"}, {"versioned_ensembl_gene_id":"ENSG00000253080.1","gene_symbol":"RNA5SP373","gene_name":"RNA, 5S ribosomal pseudogene 373 [Source:HGNC Symbol;Acc:HGNC:43273]","synonyms":"RN5S373","biotype":"rRNA","ncbi_id":"100873631","summary":null,"start":111339527,"end":111339621,"strand":1,"description":"RNA, 5S ribosomal pseudogene 373 [Source:HGNC Symbol;Acc:HGNC:43273]"}, {"versioned_ensembl_gene_id":"ENSG00000282422.1","gene_symbol":"AC243913.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28706490,"end":28706648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264014.1","gene_symbol":"MIR4253","gene_name":"microRNA 4253 [Source:HGNC Symbol;Acc:HGNC:38231]","synonyms":"hsa-mir-4253","biotype":"miRNA","ncbi_id":"100422914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22863159,"end":22863226,"strand":-1,"description":"microRNA 4253 [Source:HGNC Symbol;Acc:HGNC:38231]"}, {"versioned_ensembl_gene_id":"ENSG00000274878.1","gene_symbol":"DLEU2_3","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50049591,"end":50049663,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]"}, {"versioned_ensembl_gene_id":"ENSG00000252604.1","gene_symbol":"RNU2-44P","gene_name":"RNA, U2 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48537]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481648","summary":null,"start":154790291,"end":154790484,"strand":1,"description":"RNA, U2 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48537]"}, {"versioned_ensembl_gene_id":"ENSG00000207199.1","gene_symbol":"SNORD38","gene_name":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":39018615,"end":39018683,"strand":-1,"description":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]"}, {"versioned_ensembl_gene_id":"ENSG00000278108.1","gene_symbol":"MIR6757","gene_name":"microRNA 6757 [Source:HGNC Symbol;Acc:HGNC:50160]","synonyms":"hsa-mir-6757","biotype":"miRNA","ncbi_id":"102466193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53056944,"end":53057012,"strand":1,"description":"microRNA 6757 [Source:HGNC Symbol;Acc:HGNC:50160]"}, {"versioned_ensembl_gene_id":"ENSG00000273912.1","gene_symbol":"MIR8068","gene_name":"microRNA 8068 [Source:HGNC Symbol;Acc:HGNC:50238]","synonyms":"hsa-mir-8068","biotype":"miRNA","ncbi_id":"102466876","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28477481,"end":28477548,"strand":-1,"description":"microRNA 8068 [Source:HGNC Symbol;Acc:HGNC:50238]"}, {"versioned_ensembl_gene_id":"ENSG00000199700.1","gene_symbol":"RNU6-223P","gene_name":"RNA, U6 small nuclear 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:47186]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481248","summary":null,"start":135960703,"end":135960809,"strand":1,"description":"RNA, U6 small nuclear 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:47186]"}, {"versioned_ensembl_gene_id":"ENSG00000206649.1","gene_symbol":"SNORA20","gene_name":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":80316939,"end":80317069,"strand":-1,"description":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]"}, {"versioned_ensembl_gene_id":"ENSG00000238761.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":112371004,"end":112371107,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000276982.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000207421.1","gene_symbol":"SNORD38B","gene_name":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]","synonyms":"U38B,RNU38B,U38B,RNU38B","biotype":"snoRNA","ncbi_id":"94163","summary":null,"start":44778390,"end":44778456,"strand":1,"description":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]"}, {"versioned_ensembl_gene_id":"ENSG00000242436.3","gene_symbol":"RN7SL789P","gene_name":"RNA, 7SL, cytoplasmic 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:46805]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479508","summary":null,"start":32655016,"end":32655308,"strand":-1,"description":"RNA, 7SL, cytoplasmic 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:46805]"}, {"versioned_ensembl_gene_id":"ENSG00000268991.2","gene_symbol":"FAM231B","gene_name":"family with sequence similarity 231 member B [Source:HGNC Symbol;Acc:HGNC:49506]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100133301","summary":null,"start":16539066,"end":16539575,"strand":1,"description":"family with sequence similarity 231 member B [Source:HGNC Symbol;Acc:HGNC:49506]"}, {"versioned_ensembl_gene_id":"ENSG00000222076.1","gene_symbol":"RNU2-3P","gene_name":"RNA, U2 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10153]","synonyms":"U2,RNU2P1","biotype":"snRNA","ncbi_id":"26854","summary":null,"start":95745804,"end":95745994,"strand":1,"description":"RNA, U2 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10153]"}, {"versioned_ensembl_gene_id":"ENSG00000266503.2","gene_symbol":"RN7SL162P","gene_name":"RNA, 7SL, cytoplasmic 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:46178]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481828","summary":null,"start":28642979,"end":28643270,"strand":-1,"description":"RNA, 7SL, cytoplasmic 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:46178]"}, {"versioned_ensembl_gene_id":"ENSG00000265105.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747821,"end":29747922,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252626.1","gene_symbol":"RNU6-1308P","gene_name":"RNA, U6 small nuclear 1308, pseudogene [Source:HGNC Symbol;Acc:HGNC:48271]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480137","summary":null,"start":107007568,"end":107007670,"strand":1,"description":"RNA, U6 small nuclear 1308, pseudogene [Source:HGNC Symbol;Acc:HGNC:48271]"}, {"versioned_ensembl_gene_id":"ENSG00000202050.1","gene_symbol":"RNU6-391P","gene_name":"RNA, U6 small nuclear 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:47354]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479739","summary":null,"start":24365651,"end":24365754,"strand":1,"description":"RNA, U6 small nuclear 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:47354]"}, {"versioned_ensembl_gene_id":"ENSG00000252332.1","gene_symbol":"RNU6-911P","gene_name":"RNA, U6 small nuclear 911, pseudogene [Source:HGNC Symbol;Acc:HGNC:47874]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479969","summary":null,"start":139448740,"end":139448843,"strand":1,"description":"RNA, U6 small nuclear 911, pseudogene [Source:HGNC Symbol;Acc:HGNC:47874]"}, {"versioned_ensembl_gene_id":"ENSG00000239115.1","gene_symbol":"RNU7-67P","gene_name":"RNA, U7 small nuclear 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:34163]","synonyms":"U7.67","biotype":"snRNA","ncbi_id":"100151665","summary":null,"start":101307367,"end":101307428,"strand":1,"description":"RNA, U7 small nuclear 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:34163]"}, {"versioned_ensembl_gene_id":"ENSG00000212424.1","gene_symbol":"RNU1-119P","gene_name":"RNA, U1 small nuclear 119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48461]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480668","summary":null,"start":44884616,"end":44884780,"strand":1,"description":"RNA, U1 small nuclear 119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48461]"}, {"versioned_ensembl_gene_id":"ENSG00000264102.1","gene_symbol":"MIR4688","gene_name":"microRNA 4688 [Source:HGNC Symbol;Acc:HGNC:41897]","synonyms":"hsa-mir-4688","biotype":"miRNA","ncbi_id":"100616368","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46376402,"end":46376484,"strand":1,"description":"microRNA 4688 [Source:HGNC Symbol;Acc:HGNC:41897]"}, {"versioned_ensembl_gene_id":"ENSG00000202263.1","gene_symbol":"RNA5SP22","gene_name":"RNA, 5S ribosomal pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42590]","synonyms":"RN5S22","biotype":"rRNA","ncbi_id":"100873277","summary":null,"start":78094807,"end":78094915,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42590]"}, {"versioned_ensembl_gene_id":"ENSG00000207146.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108676951,"end":108677057,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221406.1","gene_symbol":"MIR320B2","gene_name":"microRNA 320b-2 [Source:HGNC Symbol;Acc:HGNC:35256]","synonyms":"MIRN320B2,hsa-mir-320b-2","biotype":"miRNA","ncbi_id":"100313769","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":224257004,"end":224257141,"strand":-1,"description":"microRNA 320b-2 [Source:HGNC Symbol;Acc:HGNC:35256]"}, {"versioned_ensembl_gene_id":"ENSG00000200670.1","gene_symbol":"RNU6-912P","gene_name":"RNA, U6 small nuclear 912, pseudogene [Source:HGNC Symbol;Acc:HGNC:47875]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479970","summary":null,"start":65814672,"end":65814775,"strand":1,"description":"RNA, U6 small nuclear 912, pseudogene [Source:HGNC Symbol;Acc:HGNC:47875]"}, {"versioned_ensembl_gene_id":"ENSG00000207077.1","gene_symbol":"RNU6-1119P","gene_name":"RNA, U6 small nuclear 1119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48082]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481533","summary":null,"start":100153672,"end":100153779,"strand":1,"description":"RNA, U6 small nuclear 1119, pseudogene [Source:HGNC Symbol;Acc:HGNC:48082]"}, {"versioned_ensembl_gene_id":"ENSG00000252261.1","gene_symbol":"RNA5SP262","gene_name":"RNA, 5S ribosomal pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:43162]","synonyms":"RN5S262","biotype":"rRNA","ncbi_id":"100873516","summary":null,"start":32192028,"end":32192153,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 262 [Source:HGNC Symbol;Acc:HGNC:43162]"}, {"versioned_ensembl_gene_id":"ENSG00000200064.1","gene_symbol":"RNY4P9","gene_name":"RNA, Ro-associated Y4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:34058]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379300","summary":null,"start":49908634,"end":49908730,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:34058]"}, {"versioned_ensembl_gene_id":"ENSG00000276162.1","gene_symbol":"MIR5739","gene_name":"microRNA 5739 [Source:HGNC Symbol;Acc:HGNC:49977]","synonyms":"hsa-mir-5739","biotype":"miRNA","ncbi_id":"102466081","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28459869,"end":28459948,"strand":1,"description":"microRNA 5739 [Source:HGNC Symbol;Acc:HGNC:49977]"}, {"versioned_ensembl_gene_id":"ENSG00000283385.1","gene_symbol":"MIR4524A","gene_name":"microRNA 4524a [Source:HGNC Symbol;Acc:HGNC:41771]","synonyms":"MIR4524,hsa-mir-4524","biotype":"miRNA","ncbi_id":"100616316","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69099564,"end":69099632,"strand":-1,"description":"microRNA 4524a [Source:HGNC Symbol;Acc:HGNC:41771]"}, {"versioned_ensembl_gene_id":"ENSG00000263918.1","gene_symbol":"MIR3670-1","gene_name":"microRNA 3670-1 [Source:HGNC Symbol;Acc:HGNC:38997]","synonyms":"MIR3670,hsa-mir-3670","biotype":"miRNA","ncbi_id":"100500910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14907717,"end":14907781,"strand":1,"description":"microRNA 3670-1 [Source:HGNC Symbol;Acc:HGNC:38997]"}, {"versioned_ensembl_gene_id":"ENSG00000197889.9","gene_symbol":"MEIG1","gene_name":"meiosis/spermiogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23429]","synonyms":"SPATA39,bA2K17.3","biotype":"protein_coding","ncbi_id":"644890","summary":null,"start":14959439,"end":14988050,"strand":1,"description":"meiosis/spermiogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23429]"}, {"versioned_ensembl_gene_id":"ENSG00000179044.15","gene_symbol":"EXOC3L1","gene_name":"exocyst complex component 3 like 1 [Source:HGNC Symbol;Acc:HGNC:27540]","synonyms":"FLJ35587,FLJ35539,EXOC3L","biotype":"protein_coding","ncbi_id":"283849","summary":null,"start":67184366,"end":67190204,"strand":-1,"description":"exocyst complex component 3 like 1 [Source:HGNC Symbol;Acc:HGNC:27540]"}, {"versioned_ensembl_gene_id":"ENSG00000277052.1","gene_symbol":"MIR6763","gene_name":"microRNA 6763 [Source:HGNC Symbol;Acc:HGNC:50139]","synonyms":"hsa-mir-6763","biotype":"miRNA","ncbi_id":"102465975","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132581997,"end":132582061,"strand":1,"description":"microRNA 6763 [Source:HGNC Symbol;Acc:HGNC:50139]"}, {"versioned_ensembl_gene_id":"ENSG00000223321.1","gene_symbol":"RN7SKP293","gene_name":"RNA, 7SK small nuclear pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:46017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480923","summary":null,"start":12406486,"end":12406781,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:46017]"}, {"versioned_ensembl_gene_id":"ENSG00000221333.1","gene_symbol":"MIR548K","gene_name":"microRNA 548k [Source:HGNC Symbol;Acc:HGNC:35285]","synonyms":"MIRN548K,hsa-mir-548k","biotype":"miRNA","ncbi_id":"100313770","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70283955,"end":70284070,"strand":1,"description":"microRNA 548k [Source:HGNC Symbol;Acc:HGNC:35285]"}, {"versioned_ensembl_gene_id":"ENSG00000199373.1","gene_symbol":"RNA5SP453","gene_name":"RNA, 5S ribosomal pseudogene 453 [Source:HGNC Symbol;Acc:HGNC:43353]","synonyms":"RN5S453","biotype":"rRNA","ncbi_id":"100873698","summary":null,"start":32176050,"end":32176168,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 453 [Source:HGNC Symbol;Acc:HGNC:43353]"}, {"versioned_ensembl_gene_id":"ENSG00000273516.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":121008362,"end":121008507,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000238616.1","gene_symbol":"RNU6-300P","gene_name":"RNA, U6 small nuclear 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:47263]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479700","summary":null,"start":151201341,"end":151201444,"strand":1,"description":"RNA, U6 small nuclear 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:47263]"}, {"versioned_ensembl_gene_id":"ENSG00000283276.1","gene_symbol":"ABBA01000935.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91374331,"end":91514157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222810.1","gene_symbol":"RNU2-68P","gene_name":"RNA, U2 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48561]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481962","summary":null,"start":72376979,"end":72377169,"strand":-1,"description":"RNA, U2 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48561]"}, {"versioned_ensembl_gene_id":"ENSG00000200356.1","gene_symbol":"RNU6-833P","gene_name":"RNA, U6 small nuclear 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:47796]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481444","summary":null,"start":73279062,"end":73279168,"strand":1,"description":"RNA, U6 small nuclear 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:47796]"}, {"versioned_ensembl_gene_id":"ENSG00000262354.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69191115,"end":69191215,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221066.1","gene_symbol":"SNORD111","gene_name":"small nucleolar RNA, C/D box 111 [Source:HGNC Symbol;Acc:HGNC:32776]","synonyms":"HBII-82","biotype":"snoRNA","ncbi_id":"692214","summary":null,"start":70538005,"end":70538098,"strand":1,"description":"small nucleolar RNA, C/D box 111 [Source:HGNC Symbol;Acc:HGNC:32776]"}, {"versioned_ensembl_gene_id":"ENSG00000253739.1","gene_symbol":"RNU6-323P","gene_name":"RNA, U6 small nuclear 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:47286]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481281","summary":null,"start":38166012,"end":38166118,"strand":-1,"description":"RNA, U6 small nuclear 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:47286]"}, {"versioned_ensembl_gene_id":"ENSG00000200613.1","gene_symbol":"RNA5SP349","gene_name":"RNA, 5S ribosomal pseudogene 349 [Source:HGNC Symbol;Acc:HGNC:43249]","synonyms":"RN5S349","biotype":"rRNA","ncbi_id":"100873611","summary":null,"start":109120878,"end":109120986,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 349 [Source:HGNC Symbol;Acc:HGNC:43249]"}, {"versioned_ensembl_gene_id":"ENSG00000252238.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":4827001,"end":4827084,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000206903.1","gene_symbol":"SNORA24B","gene_name":"small nucleolar RNA, H/ACA box 24B [Source:HGNC Symbol;Acc:HGNC:52198]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617003","summary":null,"start":65285461,"end":65285591,"strand":-1,"description":"small nucleolar RNA, H/ACA box 24B [Source:HGNC Symbol;Acc:HGNC:52198]"}, {"versioned_ensembl_gene_id":"ENSG00000201277.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":173254190,"end":173254290,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264741.1","gene_symbol":"MIR4505","gene_name":"microRNA 4505 [Source:HGNC Symbol;Acc:HGNC:41743]","synonyms":"hsa-mir-4505","biotype":"miRNA","ncbi_id":"100616158","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":73758747,"end":73758819,"strand":1,"description":"microRNA 4505 [Source:HGNC Symbol;Acc:HGNC:41743]"}, {"versioned_ensembl_gene_id":"ENSG00000221369.1","gene_symbol":"MIR548G","gene_name":"microRNA 548g [Source:HGNC Symbol;Acc:HGNC:35326]","synonyms":"MIRN548G,hsa-mir-548g","biotype":"miRNA","ncbi_id":"100313938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147344629,"end":147344717,"strand":-1,"description":"microRNA 548g [Source:HGNC Symbol;Acc:HGNC:35326]"}, {"versioned_ensembl_gene_id":"ENSG00000187510.8","gene_symbol":"PLEKHG7","gene_name":"pleckstrin homology and RhoGEF domain containing G7 [Source:HGNC Symbol;Acc:HGNC:33829]","synonyms":"FLJ46688","biotype":"protein_coding","ncbi_id":"440107","summary":null,"start":92721462,"end":92772455,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G7 [Source:HGNC Symbol;Acc:HGNC:33829]"}, {"versioned_ensembl_gene_id":"ENSG00000012983.11","gene_symbol":"MAP4K5","gene_name":"mitogen-activated protein kinase kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6867]","synonyms":"KHS1,KHS,GCKR","biotype":"protein_coding","ncbi_id":"11183","summary":"This gene encodes a member of the serine/threonine protein kinase family, that is highly similar to yeast SPS1/STE20 kinase. Yeast SPS1/STE20 functions near the beginning of the MAP kinase signal cascades that is essential for yeast pheromone response. This kinase was shown to activate Jun kinase in mammalian cells, which suggested a role in stress response. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":50418501,"end":50561126,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6867]"}, {"versioned_ensembl_gene_id":"ENSG00000151748.14","gene_symbol":"SAV1","gene_name":"salvador family WW domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:17795]","synonyms":"WWP4,WW45,salvador","biotype":"protein_coding","ncbi_id":"60485","summary":"WW domain-containing proteins are found in all eukaryotes and play an important role in the regulation of a wide variety of cellular functions such as protein degradation, transcription, and RNA splicing. This gene encodes a protein with two WW domains, a SARAH domain, and a coiled-coil region and is ubiquitously expressed in adult tissues. This protein binds to MST1 (mammalian sterile 20-like kinase 1) and promotes MST1-induced apoptosis. It has also been shown to bind to HAX1 (hematopoietic cell-specific protein 1 (HS1)-associated protein X-1) and to attenuate the anti-apoptotic effects of HAX1. Studies in human and mouse suggest this gene acts as a tumor suppressor. [provided by RefSeq, Aug 2012]","start":50632058,"end":50668331,"strand":-1,"description":"salvador family WW domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:17795]"}, {"versioned_ensembl_gene_id":"ENSG00000237848.1","gene_symbol":"AL606489.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204394541,"end":204394774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261065.1","gene_symbol":"AL592146.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204131062,"end":204131966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126456.15","gene_symbol":"IRF3","gene_name":"interferon regulatory factor 3 [Source:HGNC Symbol;Acc:HGNC:6118]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3661","summary":"This gene encodes a member of the interferon regulatory transcription factor (IRF) family. The encoded protein is found in an inactive cytoplasmic form that upon serine/threonine phosphorylation forms a complex with CREBBP. This complex translocates to the nucleus and activates the transcription of interferons alpha and beta, as well as other interferon-induced genes. The protein plays an important role in the innate immune response against DNA and RNA viruses. Mutations in this gene are associated with Encephalopathy, acute, infection-induced, herpes-specific, 7. [provided by RefSeq, Sep 2020]","start":49659569,"end":49665875,"strand":-1,"description":"interferon regulatory factor 3 [Source:HGNC Symbol;Acc:HGNC:6118]"}, {"versioned_ensembl_gene_id":"ENSG00000270179.1","gene_symbol":"AP002840.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113368478,"end":113369117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149292.16","gene_symbol":"TTC12","gene_name":"tetratricopeptide repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:23700]","synonyms":"TPARM,FLJ20535,FLJ13859","biotype":"protein_coding","ncbi_id":"54970","summary":null,"start":113314529,"end":113383544,"strand":1,"description":"tetratricopeptide repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:23700]"}, {"versioned_ensembl_gene_id":"ENSG00000141858.11","gene_symbol":"SAMD1","gene_name":"sterile alpha motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17958]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90378","summary":null,"start":14087840,"end":14091036,"strand":-1,"description":"sterile alpha motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17958]"}, {"versioned_ensembl_gene_id":"ENSG00000251678.1","gene_symbol":"AC027343.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7344579,"end":7345921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247732.2","gene_symbol":"AC091951.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7290823,"end":7296345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112941.13","gene_symbol":"PAPD7","gene_name":"poly(A) RNA polymerase D7, non-canonical [Source:HGNC Symbol;Acc:HGNC:16705]","synonyms":"TRF4-1,TRF4,POLS,POLK,LAK-1","biotype":"protein_coding","ncbi_id":"11044","summary":"The protein encoded by this gene is a DNA polymerase that is likely involved in DNA repair. In addition, the encoded protein may be required for sister chromatid adhesion. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jan 2010]","start":6713007,"end":6757048,"strand":1,"description":"poly(A) RNA polymerase D7, non-canonical [Source:HGNC Symbol;Acc:HGNC:16705]"}, {"versioned_ensembl_gene_id":"ENSG00000262099.1","gene_symbol":"AC004148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5469092,"end":5470360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271963.1","gene_symbol":"AC026786.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133115692,"end":133122340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247970.2","gene_symbol":"AL160313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99604556,"end":99625740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250842.1","gene_symbol":"AC137770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145337932,"end":145381670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213326.4","gene_symbol":"RPS7P11","gene_name":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644315","summary":null,"start":46721582,"end":46722167,"strand":-1,"description":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]"}, {"versioned_ensembl_gene_id":"ENSG00000262660.1","gene_symbol":"AC139530.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":81703371,"end":81720539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262814.7","gene_symbol":"MRPL12","gene_name":"mitochondrial ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10378]","synonyms":"RPML12,MRPL7/L12,MRPL7","biotype":"protein_coding","ncbi_id":"6182","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which forms homodimers. In prokaryotic ribosomes, two L7/L12 dimers and one L10 protein form the L8 protein complex. [provided by RefSeq, Jul 2008]","start":81703357,"end":81707526,"strand":1,"description":"mitochondrial ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10378]"}, {"versioned_ensembl_gene_id":"ENSG00000058673.16","gene_symbol":"ZC3H11A","gene_name":"zinc finger CCCH-type containing 11A [Source:HGNC Symbol;Acc:HGNC:29093]","synonyms":"ZC3HDC11A,KIAA0663","biotype":"protein_coding","ncbi_id":"9877","summary":null,"start":203795654,"end":203854999,"strand":1,"description":"zinc finger CCCH-type containing 11A [Source:HGNC Symbol;Acc:HGNC:29093]"}, {"versioned_ensembl_gene_id":"ENSG00000243904.1","gene_symbol":"RPSAP5","gene_name":"ribosomal protein SA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:20139]","synonyms":"LAMR1P5","biotype":"processed_pseudogene","ncbi_id":"319129","summary":null,"start":103374033,"end":103374916,"strand":-1,"description":"ribosomal protein SA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:20139]"}, {"versioned_ensembl_gene_id":"ENSG00000266364.1","gene_symbol":"AC087499.8","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20633034,"end":20633259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229402.1","gene_symbol":"AL162151.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99158416,"end":99159669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232573.1","gene_symbol":"RPL3P4","gene_name":"ribosomal protein L3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326307","summary":null,"start":98972879,"end":98973301,"strand":-1,"description":"ribosomal protein L3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19805]"}, {"versioned_ensembl_gene_id":"ENSG00000176605.7","gene_symbol":"C14orf177","gene_name":"chromosome 14 open reading frame 177 [Source:HGNC Symbol;Acc:HGNC:26375]","synonyms":"FLJ25773","biotype":"protein_coding","ncbi_id":"283598","summary":null,"start":98711613,"end":98717761,"strand":1,"description":"chromosome 14 open reading frame 177 [Source:HGNC Symbol;Acc:HGNC:26375]"}, {"versioned_ensembl_gene_id":"ENSG00000231258.2","gene_symbol":"ZSWIM5P2","gene_name":"zinc finger SWIM-type containing 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43769]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132201","summary":null,"start":20583758,"end":20591180,"strand":-1,"description":"zinc finger SWIM-type containing 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43769]"}, {"versioned_ensembl_gene_id":"ENSG00000235323.2","gene_symbol":"COTL1P2","gene_name":"coactosin-like F-actin binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24322]","synonyms":"CLPSMCR","biotype":"processed_pseudogene","ncbi_id":"347720","summary":null,"start":20564538,"end":20564889,"strand":1,"description":"coactosin-like F-actin binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24322]"}, {"versioned_ensembl_gene_id":"ENSG00000259110.1","gene_symbol":"LINC02304","gene_name":"long intergenic non-protein coding RNA 2304 [Source:HGNC Symbol;Acc:HGNC:53223]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370648","summary":null,"start":97154857,"end":97158736,"strand":1,"description":"long intergenic non-protein coding RNA 2304 [Source:HGNC Symbol;Acc:HGNC:53223]"}, {"versioned_ensembl_gene_id":"ENSG00000263946.1","gene_symbol":"AC015818.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20554971,"end":20559410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137726.16","gene_symbol":"FXYD6","gene_name":"FXYD domain containing ion transport regulator 6 [Source:HGNC Symbol;Acc:HGNC:4030]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53826","summary":"This gene encodes a member of the FXYD family of transmembrane proteins. This particular protein encodes phosphohippolin, which likely affects the activity of Na,K-ATPase. Multiple alternatively spliced transcript variants encoding the same protein have been described. Related pseudogenes have been identified on chromosomes 10 and X. Read-through transcripts have been observed between this locus and the downstream sodium/potassium-transporting ATPase subunit gamma (FXYD2, GeneID 486) locus.[provided by RefSeq, Feb 2011]","start":117836976,"end":117877486,"strand":-1,"description":"FXYD domain containing ion transport regulator 6 [Source:HGNC Symbol;Acc:HGNC:4030]"}, {"versioned_ensembl_gene_id":"ENSG00000258401.1","gene_symbol":"AL512361.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49373966,"end":49374383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224025.2","gene_symbol":"AL353616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68609125,"end":68611984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258392.1","gene_symbol":"RPA2P1","gene_name":"replication protein A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19676]","synonyms":"RPA2P","biotype":"processed_pseudogene","ncbi_id":"326628","summary":null,"start":46996454,"end":46997174,"strand":1,"description":"replication protein A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19676]"}, {"versioned_ensembl_gene_id":"ENSG00000105357.15","gene_symbol":"MYH14","gene_name":"myosin heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:23212]","synonyms":"MYH17,MHC16,KIAA2034,FLJ13881,DFNA4","biotype":"protein_coding","ncbi_id":"79784","summary":"This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-14 (MYO14). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":50188186,"end":50310545,"strand":1,"description":"myosin heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:23212]"}, {"versioned_ensembl_gene_id":"ENSG00000267815.1","gene_symbol":"AC008655.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50310022,"end":50310539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133055.8","gene_symbol":"MYBPH","gene_name":"myosin binding protein H [Source:HGNC Symbol;Acc:HGNC:7552]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4608","summary":null,"start":203167811,"end":203175813,"strand":-1,"description":"myosin binding protein H [Source:HGNC Symbol;Acc:HGNC:7552]"}, {"versioned_ensembl_gene_id":"ENSG00000188766.12","gene_symbol":"SPRED3","gene_name":"sprouty related EVH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"399473","summary":"This gene encodes a protein with a C-terminal Sprouty-like cysteine-rich domain (SRY) and an N-terminal Ena/Vasodilator-stimulated phosphoprotein (VASP) homology-1 (EVH-1) domain. The encoded protein is a member of a family of proteins that negatively regulates mitogen-activated protein (MAP) kinase signaling, particularly during organogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":38388421,"end":38399587,"strand":1,"description":"sprouty related EVH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31041]"}, {"versioned_ensembl_gene_id":"ENSG00000258845.1","gene_symbol":"AL139354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45567995,"end":45569069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229567.1","gene_symbol":"AL139421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93278961,"end":93279129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237003.1","gene_symbol":"AC126124.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93190740,"end":93191060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165684.4","gene_symbol":"SNAPC4","gene_name":"small nuclear RNA activating complex polypeptide 4 [Source:HGNC Symbol;Acc:HGNC:11137]","synonyms":"FLJ13451,SNAP190,PTFalpha","biotype":"protein_coding","ncbi_id":"6621","summary":"This gene encodes the largest subunit of the small nuclear RNA-activating protein (SNAP) complex. The encoded protein contains a Myb DNA-binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis. [provided by RefSeq, Jul 2016]","start":136375577,"end":136400168,"strand":-1,"description":"small nuclear RNA activating complex polypeptide 4 [Source:HGNC Symbol;Acc:HGNC:11137]"}, {"versioned_ensembl_gene_id":"ENSG00000183475.12","gene_symbol":"ASB7","gene_name":"ankyrin repeat and SOCS box containing 7 [Source:HGNC Symbol;Acc:HGNC:17182]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140460","summary":"The protein encoded by this gene belongs to a family of ankyrin repeat proteins that, along with four other protein families, contains a C-terminal SOCS box motif. Growing evidence suggests that the SOCS box acts as a bridge between specific substrate-binding domains and the more generic proteins that comprise a large family of E3 ubiquitin protein ligases. In this way, SOCS box containing proteins may regulate protein turnover by targeting proteins for polyubiquination and, therefore, for proteasome-mediated degradation. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":100602534,"end":100651705,"strand":1,"description":"ankyrin repeat and SOCS box containing 7 [Source:HGNC Symbol;Acc:HGNC:17182]"}, {"versioned_ensembl_gene_id":"ENSG00000108559.11","gene_symbol":"NUP88","gene_name":"nucleoporin 88 [Source:HGNC Symbol;Acc:HGNC:8067]","synonyms":"MGC8530","biotype":"protein_coding","ncbi_id":"4927","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins, a family of 50 to 100 proteins, are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene belongs to the nucleoporin family and is associated with the oncogenic nucleoporin CAN/Nup214 in a dynamic subcomplex. This protein is also overexpressed in a large number of malignant neoplasms and precancerous dysplasias. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":5360963,"end":5420160,"strand":-1,"description":"nucleoporin 88 [Source:HGNC Symbol;Acc:HGNC:8067]"}, {"versioned_ensembl_gene_id":"ENSG00000231407.5","gene_symbol":"AL354732.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170460453,"end":170532647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233703.1","gene_symbol":"AC027673.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80749632,"end":80751231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153823.18","gene_symbol":"PID1","gene_name":"phosphotyrosine interaction domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26084]","synonyms":"NYGGF4,FLJ20701","biotype":"protein_coding","ncbi_id":"55022","summary":null,"start":228850526,"end":229271285,"strand":-1,"description":"phosphotyrosine interaction domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26084]"}, {"versioned_ensembl_gene_id":"ENSG00000260919.1","gene_symbol":"AC100835.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74613194,"end":74615596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233990.1","gene_symbol":"AL353754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7833618,"end":7833957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237357.2","gene_symbol":"BX088651.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42566679,"end":42569353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175602.3","gene_symbol":"CCDC85B","gene_name":"coiled-coil domain containing 85B [Source:HGNC Symbol;Acc:HGNC:24926]","synonyms":"DIPA","biotype":"protein_coding","ncbi_id":"11007","summary":"Hepatitis delta virus (HDV) is a pathogenic human virus whose RNA genome and replication cycle resemble those of plant viroids. Delta-interacting protein A (DIPA), a cellular gene product, has been found to have homology to hepatitis delta virus antigen (HDAg). DIPA interacts with the viral antigen, HDAg, and can affect HDV replication in vitro. [provided by RefSeq, Jul 2008]","start":65890112,"end":65891635,"strand":1,"description":"coiled-coil domain containing 85B [Source:HGNC Symbol;Acc:HGNC:24926]"}, {"versioned_ensembl_gene_id":"ENSG00000174059.16","gene_symbol":"CD34","gene_name":"CD34 molecule [Source:HGNC Symbol;Acc:HGNC:1662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"947","summary":"The protein encoded by this gene may play a role in the attachment of stem cells to the bone marrow extracellular matrix or to stromal cells. This single-pass membrane protein is highly glycosylated and phosphorylated by protein kinase C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":207880972,"end":207911402,"strand":-1,"description":"CD34 molecule [Source:HGNC Symbol;Acc:HGNC:1662]"}, {"versioned_ensembl_gene_id":"ENSG00000238041.3","gene_symbol":"AP004245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56690465,"end":56690723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225497.5","gene_symbol":"KCNMA1-AS2","gene_name":"KCNMA1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51214]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929310","summary":null,"start":77147652,"end":77150100,"strand":1,"description":"KCNMA1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51214]"}, {"versioned_ensembl_gene_id":"ENSG00000279993.1","gene_symbol":"AC078925.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131025561,"end":131028060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186318.16","gene_symbol":"BACE1","gene_name":"beta-secretase 1 [Source:HGNC Symbol;Acc:HGNC:933]","synonyms":"BACE","biotype":"protein_coding","ncbi_id":"23621","summary":"This gene encodes a member of the peptidase A1 family of aspartic proteases. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protease. This transmembrane protease catalyzes the first step in the formation of amyloid beta peptide from amyloid precursor protein. Amyloid beta peptides are the main constituent of amyloid beta plaques, which accumulate in the brains of human Alzheimer's disease patients. [provided by RefSeq, Nov 2015]","start":117285207,"end":117316259,"strand":-1,"description":"beta-secretase 1 [Source:HGNC Symbol;Acc:HGNC:933]"}, {"versioned_ensembl_gene_id":"ENSG00000210049.1","gene_symbol":"MT-TF","gene_name":"mitochondrially encoded tRNA phenylalanine [Source:HGNC Symbol;Acc:HGNC:7481]","synonyms":"trnF,MTTF","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":577,"end":647,"strand":1,"description":"mitochondrially encoded tRNA phenylalanine [Source:HGNC Symbol;Acc:HGNC:7481]"}, {"versioned_ensembl_gene_id":"ENSG00000211459.2","gene_symbol":"MT-RNR1","gene_name":"mitochondrially encoded 12S RNA [Source:HGNC Symbol;Acc:HGNC:7470]","synonyms":"MTRNR1,12S","biotype":"Mt_rRNA","ncbi_id":null,"summary":null,"start":648,"end":1601,"strand":1,"description":"mitochondrially encoded 12S RNA [Source:HGNC Symbol;Acc:HGNC:7470]"}, {"versioned_ensembl_gene_id":"ENSG00000210077.1","gene_symbol":"MT-TV","gene_name":"mitochondrially encoded tRNA valine [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000198888.2","gene_symbol":"MT-ND1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 [Source:HGNC Symbol;Acc:HGNC:7455]","synonyms":"MTND1,ND1,NAD1","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3307,"end":4262,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 [Source:HGNC Symbol;Acc:HGNC:7455]"}, {"versioned_ensembl_gene_id":"ENSG00000210100.1","gene_symbol":"MT-TI","gene_name":"mitochondrially encoded tRNA isoleucine [Source:HGNC Symbol;Acc:HGNC:7488]","synonyms":"trnI,MTTI","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":4263,"end":4331,"strand":1,"description":"mitochondrially encoded tRNA isoleucine [Source:HGNC Symbol;Acc:HGNC:7488]"}, {"versioned_ensembl_gene_id":"ENSG00000210107.1","gene_symbol":"MT-TQ","gene_name":"mitochondrially encoded tRNA glutamine [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000198804.2","gene_symbol":"MT-CO1","gene_name":"mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]","synonyms":"MTCO1,COX1,COI","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5904,"end":7445,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]"}, {"versioned_ensembl_gene_id":"ENSG00000210151.2","gene_symbol":"MT-TS1","gene_name":"mitochondrially encoded tRNA serine 1 (UCN) [Source:HGNC Symbol;Acc:HGNC:7497]","synonyms":"TRNS1,MTTS1","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":7446,"end":7514,"strand":-1,"description":"mitochondrially encoded tRNA serine 1 (UCN) [Source:HGNC Symbol;Acc:HGNC:7497]"}, {"versioned_ensembl_gene_id":"ENSG00000210154.1","gene_symbol":"MT-TD","gene_name":"mitochondrially encoded tRNA aspartic acid [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000163431.12","gene_symbol":"LMOD1","gene_name":"leiomodin 1 [Source:HGNC Symbol;Acc:HGNC:6647]","synonyms":"D1,64kD,1D","biotype":"protein_coding","ncbi_id":"25802","summary":" The leiomodin 1 protein has a putative membrane-spanning region and 2 types of tandemly repeated blocks. The transcript is expressed in all tissues tested, with the highest levels in thyroid, eye muscle, skeletal muscle, and ovary. Increased expression of leiomodin 1 may be linked to Graves' disease and thyroid-associated ophthalmopathy. [provided by RefSeq, Jul 2008]","start":201896452,"end":201946588,"strand":-1,"description":"leiomodin 1 [Source:HGNC Symbol;Acc:HGNC:6647]"}, {"versioned_ensembl_gene_id":"ENSG00000170549.3","gene_symbol":"IRX1","gene_name":"iroquois homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14358]","synonyms":"IRX-5","biotype":"protein_coding","ncbi_id":"79192","summary":"This gene encodes a member of the Iroquois homeobox protein family. Homeobox genes in this family are involved in pattern formation in the embryo. The gene product has been identified as a tumor suppressor in gastric (PMID: 21602894, 20440264) and head and neck cancers (PMID: 18559491). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Dec 2011]","start":3596054,"end":3601403,"strand":1,"description":"iroquois homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14358]"}, {"versioned_ensembl_gene_id":"ENSG00000228253.1","gene_symbol":"MT-ATP8","gene_name":"mitochondrially encoded ATP synthase 8 [Source:HGNC Symbol;Acc:HGNC:7415]","synonyms":"MTATP8,ATP8,A6L","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8366,"end":8572,"strand":1,"description":"mitochondrially encoded ATP synthase 8 [Source:HGNC Symbol;Acc:HGNC:7415]"}, {"versioned_ensembl_gene_id":"ENSG00000241978.9","gene_symbol":"AKAP2","gene_name":"A-kinase anchoring protein 2 [Source:HGNC Symbol;Acc:HGNC:372]","synonyms":"PRKA2,MISP2,KIAA0920,DKFZp564L0716,AKAP-KL","biotype":"protein_coding","ncbi_id":"11217","summary":null,"start":110048598,"end":110172512,"strand":1,"description":"A-kinase anchoring protein 2 [Source:HGNC Symbol;Acc:HGNC:372]"}, {"versioned_ensembl_gene_id":"ENSG00000259603.1","gene_symbol":"AC016595.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3596211,"end":3600188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198899.2","gene_symbol":"MT-ATP6","gene_name":"mitochondrially encoded ATP synthase 6 [Source:HGNC Symbol;Acc:HGNC:7414]","synonyms":"ATP6,Su6m,RP,MTATP6,ATPase-6","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8527,"end":9207,"strand":1,"description":"mitochondrially encoded ATP synthase 6 [Source:HGNC Symbol;Acc:HGNC:7414]"}, {"versioned_ensembl_gene_id":"ENSG00000258820.5","gene_symbol":"AF111167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75259411,"end":75271950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272154.4","gene_symbol":"AC244517.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141100242,"end":141174391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235754.7","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"NG20,G3a,ApoM","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31643159,"end":31648952,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000235219.1","gene_symbol":"AC236972.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153203044,"end":153205534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268870.1","gene_symbol":"AC008758.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12391949,"end":12441082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198938.2","gene_symbol":"MT-CO3","gene_name":"mitochondrially encoded cytochrome c oxidase III [Source:HGNC Symbol;Acc:HGNC:7422]","synonyms":"COIII,CO3,MTCO3,COX3","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":9207,"end":9990,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III [Source:HGNC 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core subunit 4L [Source:HGNC Symbol;Acc:HGNC:7460]","synonyms":"ND4L,NAD4L,MTND4L","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10470,"end":10766,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L [Source:HGNC Symbol;Acc:HGNC:7460]"}, {"versioned_ensembl_gene_id":"ENSG00000156575.2","gene_symbol":"PRG3","gene_name":"proteoglycan 3, pro eosinophil major basic protein 2 [Source:HGNC Symbol;Acc:HGNC:9363]","synonyms":"MBPH,MBP2","biotype":"protein_coding","ncbi_id":"10394","summary":null,"start":57376769,"end":57381150,"strand":-1,"description":"proteoglycan 3, pro eosinophil major basic protein 2 [Source:HGNC Symbol;Acc:HGNC:9363]"}, {"versioned_ensembl_gene_id":"ENSG00000117834.12","gene_symbol":"SLC5A9","gene_name":"solute carrier family 5 member 9 [Source:HGNC Symbol;Acc:HGNC:22146]","synonyms":"SGLT4","biotype":"protein_coding","ncbi_id":"200010","summary":null,"start":48222685,"end":48248644,"strand":1,"description":"solute carrier family 5 member 9 [Source:HGNC Symbol;Acc:HGNC:22146]"}, {"versioned_ensembl_gene_id":"ENSG00000198886.2","gene_symbol":"MT-ND4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 [Source:HGNC Symbol;Acc:HGNC:7459]","synonyms":"ND4,NAD4,MTND4,LHON","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10760,"end":12137,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 [Source:HGNC Symbol;Acc:HGNC:7459]"}, {"versioned_ensembl_gene_id":"ENSG00000233452.6","gene_symbol":"STXBP5-AS1","gene_name":"STXBP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44183]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729178","summary":null,"start":146841901,"end":147204614,"strand":-1,"description":"STXBP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44183]"}, {"versioned_ensembl_gene_id":"ENSG00000226752.9","gene_symbol":"PSMD5-AS1","gene_name":"PSMD5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27367]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"253039","summary":null,"start":120824828,"end":120854385,"strand":1,"description":"PSMD5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27367]"}, {"versioned_ensembl_gene_id":"ENSG00000210176.1","gene_symbol":"MT-TH","gene_name":"mitochondrially encoded tRNA histidine [Source:HGNC Symbol;Acc:HGNC:7487]","synonyms":"MTTH,trnH","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12138,"end":12206,"strand":1,"description":"mitochondrially encoded tRNA histidine [Source:HGNC Symbol;Acc:HGNC:7487]"}, {"versioned_ensembl_gene_id":"ENSG00000170482.16","gene_symbol":"SLC23A1","gene_name":"solute carrier family 23 member 1 [Source:HGNC Symbol;Acc:HGNC:10974]","synonyms":"YSPL3,SVCT1,SLC23A2","biotype":"protein_coding","ncbi_id":"9963","summary":"The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously, this gene had an official symbol of SLC23A2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":139367196,"end":139384553,"strand":-1,"description":"solute carrier family 23 member 1 [Source:HGNC Symbol;Acc:HGNC:10974]"}, {"versioned_ensembl_gene_id":"ENSG00000210184.1","gene_symbol":"MT-TS2","gene_name":"mitochondrially encoded tRNA serine 2 (AGU/C) [Source:HGNC Symbol;Acc:HGNC:7498]","synonyms":"TRNS2,RP8,MTTS2","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12207,"end":12265,"strand":1,"description":"mitochondrially encoded tRNA serine 2 (AGU/C) [Source:HGNC Symbol;Acc:HGNC:7498]"}, {"versioned_ensembl_gene_id":"ENSG00000210191.1","gene_symbol":"MT-TL2","gene_name":"mitochondrially encoded tRNA leucine 2 (CUN) [Source:HGNC Symbol;Acc:HGNC:7491]","synonyms":"TRNL2,MTTL2","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":12266,"end":12336,"strand":1,"description":"mitochondrially encoded tRNA leucine 2 (CUN) [Source:HGNC Symbol;Acc:HGNC:7491]"}, {"versioned_ensembl_gene_id":"ENSG00000273010.1","gene_symbol":"AL360270.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110963302,"end":110964649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198786.2","gene_symbol":"MT-ND5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 [Source:HGNC Symbol;Acc:HGNC:7461]","synonyms":"MTND5,ND5,NAD5","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12337,"end":14148,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 [Source:HGNC Symbol;Acc:HGNC:7461]"}, {"versioned_ensembl_gene_id":"ENSG00000228872.2","gene_symbol":"AC096664.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63717122,"end":63717899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259413.2","gene_symbol":"AC011270.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78382573,"end":78383155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278054.1","gene_symbol":"AL591926.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41647825,"end":41648035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275493.1","gene_symbol":"FAM27D1","gene_name":"family with sequence similarity 27 member D1 [Source:HGNC Symbol;Acc:HGNC:32015]","synonyms":"OTTHUMG00000013267","biotype":"processed_pseudogene","ncbi_id":"724094","summary":null,"start":41644430,"end":41644770,"strand":-1,"description":"family with sequence similarity 27 member D1 [Source:HGNC Symbol;Acc:HGNC:32015]"}, {"versioned_ensembl_gene_id":"ENSG00000198695.2","gene_symbol":"MT-ND6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 [Source:HGNC Symbol;Acc:HGNC:7462]","synonyms":"ND6,NAD6,MTND6","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14149,"end":14673,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 [Source:HGNC Symbol;Acc:HGNC:7462]"}, {"versioned_ensembl_gene_id":"ENSG00000099290.15","gene_symbol":"WASHC2A","gene_name":"WASH complex subunit 2A [Source:HGNC Symbol;Acc:HGNC:23416]","synonyms":"FAM21B,FAM21A,bA98I6.1,bA56A21.1,FLJ10824","biotype":"protein_coding","ncbi_id":"387680","summary":null,"start":50067888,"end":50133506,"strand":1,"description":"WASH complex subunit 2A [Source:HGNC Symbol;Acc:HGNC:23416]"}, {"versioned_ensembl_gene_id":"ENSG00000258630.1","gene_symbol":"LINC02292","gene_name":"long intergenic non-protein coding RNA 2292 [Source:HGNC Symbol;Acc:HGNC:53208]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929080","summary":null,"start":95329584,"end":95335504,"strand":1,"description":"long intergenic non-protein coding RNA 2292 [Source:HGNC Symbol;Acc:HGNC:53208]"}, {"versioned_ensembl_gene_id":"ENSG00000210194.1","gene_symbol":"MT-TE","gene_name":"mitochondrially encoded tRNA glutamic acid [Source:HGNC Symbol;Acc:HGNC:7479]","synonyms":"trnE,MTTE","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":14674,"end":14742,"strand":-1,"description":"mitochondrially encoded tRNA glutamic acid [Source:HGNC Symbol;Acc:HGNC:7479]"}, {"versioned_ensembl_gene_id":"ENSG00000224077.1","gene_symbol":"AP000936.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117098987,"end":117108170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198727.2","gene_symbol":"MT-CYB","gene_name":"mitochondrially encoded cytochrome b [Source:HGNC Symbol;Acc:HGNC:7427]","synonyms":"UQCR3,MTCYB,CYTB,COB","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14747,"end":15887,"strand":1,"description":"mitochondrially encoded cytochrome b [Source:HGNC Symbol;Acc:HGNC:7427]"}, {"versioned_ensembl_gene_id":"ENSG00000279983.1","gene_symbol":"AC244517.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":141223372,"end":141245861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280200.1","gene_symbol":"AC073862.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130976786,"end":130978812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143119.12","gene_symbol":"CD53","gene_name":"CD53 molecule [Source:HGNC Symbol;Acc:HGNC:1686]","synonyms":"TSPAN25,MOX44","biotype":"protein_coding","ncbi_id":"963","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins. It contributes to the transduction of CD2-generated signals in T cells and natural killer cells and has been suggested to play a role in growth regulation. Familial deficiency of this gene has been linked to an immunodeficiency associated with recurrent infectious diseases caused by bacteria, fungi and viruses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":110873154,"end":110899928,"strand":1,"description":"CD53 molecule [Source:HGNC Symbol;Acc:HGNC:1686]"}, {"versioned_ensembl_gene_id":"ENSG00000211968.3","gene_symbol":"IGHV1-58","gene_name":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28464","summary":null,"start":106622357,"end":106622855,"strand":-1,"description":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]"}, {"versioned_ensembl_gene_id":"ENSG00000210195.2","gene_symbol":"MT-TT","gene_name":"mitochondrially encoded tRNA threonine [Source:HGNC Symbol;Acc:HGNC:7499]","synonyms":"trnT,MTTT,LIMM","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":15888,"end":15953,"strand":1,"description":"mitochondrially encoded tRNA threonine [Source:HGNC Symbol;Acc:HGNC:7499]"}, {"versioned_ensembl_gene_id":"ENSG00000211966.2","gene_symbol":"IGHV5-51","gene_name":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28388","summary":null,"start":106578744,"end":106579236,"strand":-1,"description":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]"}, {"versioned_ensembl_gene_id":"ENSG00000210196.2","gene_symbol":"MT-TP","gene_name":"mitochondrially encoded tRNA proline [Source:HGNC Symbol;Acc:HGNC:7494]","synonyms":"trnP,MTTP","biotype":"Mt_tRNA","ncbi_id":null,"summary":null,"start":15956,"end":16023,"strand":-1,"description":"mitochondrially encoded tRNA proline [Source:HGNC Symbol;Acc:HGNC:7494]"}, {"versioned_ensembl_gene_id":"ENSG00000256108.1","gene_symbol":"AC135586.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132745156,"end":132745729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170409.7","gene_symbol":"AC091390.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102327256,"end":102329530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260469.2","gene_symbol":"C15orf59-AS1","gene_name":"C15orf59 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51422]","synonyms":"TCONS_00023459","biotype":"lincRNA","ncbi_id":"101929221","summary":null,"start":73752317,"end":73770613,"strand":1,"description":"C15orf59 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51422]"}, {"versioned_ensembl_gene_id":"ENSG00000116962.14","gene_symbol":"NID1","gene_name":"nidogen 1 [Source:HGNC Symbol;Acc:HGNC:7821]","synonyms":"NID,entactin","biotype":"protein_coding","ncbi_id":"4811","summary":"This gene encodes a member of the nidogen family of basement membrane glycoproteins. The protein interacts with several other components of basement membranes, and may play a role in cell interactions with the extracellular matrix. [provided by RefSeq, Jul 2008]","start":235975830,"end":236065162,"strand":-1,"description":"nidogen 1 [Source:HGNC Symbol;Acc:HGNC:7821]"}, {"versioned_ensembl_gene_id":"ENSG00000279096.2","gene_symbol":"AL356289.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48102068,"end":48104736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283562.1","gene_symbol":"IGHVIII-44","gene_name":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]","synonyms":"IGHV(III)-44","biotype":"IG_V_pseudogene","ncbi_id":"28345","summary":null,"start":106478006,"end":106478393,"strand":-1,"description":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]"}, {"versioned_ensembl_gene_id":"ENSG00000260029.2","gene_symbol":"AC007608.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50551824,"end":50553940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106780.8","gene_symbol":"MEGF9","gene_name":"multiple EGF like domains 9 [Source:HGNC Symbol;Acc:HGNC:3234]","synonyms":"EGFL5","biotype":"protein_coding","ncbi_id":"1955","summary":null,"start":120600813,"end":120714470,"strand":-1,"description":"multiple EGF like domains 9 [Source:HGNC Symbol;Acc:HGNC:3234]"}, {"versioned_ensembl_gene_id":"ENSG00000215397.3","gene_symbol":"SCRT2","gene_name":"scratch family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:15952]","synonyms":"ZNF898B","biotype":"protein_coding","ncbi_id":"85508","summary":null,"start":661596,"end":676179,"strand":-1,"description":"scratch family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:15952]"}, {"versioned_ensembl_gene_id":"ENSG00000204149.10","gene_symbol":"AGAP6","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 6 [Source:HGNC Symbol;Acc:HGNC:23466]","synonyms":"CTGLF3,bA324H6.1","biotype":"protein_coding","ncbi_id":"414189","summary":null,"start":49982190,"end":50010499,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 6 [Source:HGNC Symbol;Acc:HGNC:23466]"}, {"versioned_ensembl_gene_id":"ENSG00000160185.14","gene_symbol":"UBASH3A","gene_name":"ubiquitin associated and SH3 domain containing A [Source:HGNC Symbol;Acc:HGNC:12462]","synonyms":"TULA,STS-2,CLIP4","biotype":"protein_coding","ncbi_id":"53347","summary":"This gene encodes one of two family members belonging to the T-cell ubiquitin ligand (TULA) family. Both family members can negatively regulate T-cell signaling. This family member can facilitate growth factor withdrawal-induced apoptosis in T cells, which may occur via its interaction with AIF, an apoptosis-inducing factor. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":42403447,"end":42447681,"strand":1,"description":"ubiquitin associated and SH3 domain containing A [Source:HGNC Symbol;Acc:HGNC:12462]"}, {"versioned_ensembl_gene_id":"ENSG00000162076.12","gene_symbol":"FLYWCH2","gene_name":"FLYWCH family member 2 [Source:HGNC Symbol;Acc:HGNC:25178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114984","summary":null,"start":2883186,"end":2899382,"strand":1,"description":"FLYWCH family member 2 [Source:HGNC Symbol;Acc:HGNC:25178]"}, {"versioned_ensembl_gene_id":"ENSG00000227883.1","gene_symbol":"ATP6V0E1P4","gene_name":"ATPase H+ transporting V0 subunit e1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874504","summary":null,"start":47550196,"end":47550753,"strand":1,"description":"ATPase H+ transporting V0 subunit e1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41938]"}, {"versioned_ensembl_gene_id":"ENSG00000229833.9","gene_symbol":"PET100","gene_name":"PET100 homolog [Source:HGNC Symbol;Acc:HGNC:40038]","synonyms":"C19orf79","biotype":"protein_coding","ncbi_id":"100131801","summary":"Mitochondrial complex IV, or cytochrome c oxidase, is a large transmembrane protein complex that is part of the respiratory electron transport chain of mitochondria. The small protein encoded by this gene plays a role in the biogenesis of mitochondrial complex IV. This protein localizes to the inner mitochondrial membrane and is exposed to the intermembrane space. Mutations in this gene are associated with mitochondrial complex IV deficiency. This gene has a pseudogene on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":7629737,"end":7631956,"strand":1,"description":"PET100 homolog [Source:HGNC Symbol;Acc:HGNC:40038]"}, {"versioned_ensembl_gene_id":"ENSG00000205209.7","gene_symbol":"SCGB2B2","gene_name":"secretoglobin family 2B member 2 [Source:HGNC Symbol;Acc:HGNC:27616]","synonyms":"SCGBL,SCGB4A2","biotype":"protein_coding","ncbi_id":"284402","summary":null,"start":34593329,"end":34675699,"strand":-1,"description":"secretoglobin family 2B member 2 [Source:HGNC Symbol;Acc:HGNC:27616]"}, {"versioned_ensembl_gene_id":"ENSG00000205025.8","gene_symbol":"OR5G5P","gene_name":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56801856,"end":56820422,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]"}, {"versioned_ensembl_gene_id":"ENSG00000129951.18","gene_symbol":"PLPPR3","gene_name":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]","synonyms":"LPPR3,FLJ11535,PRG2,PRG-2","biotype":"protein_coding","ncbi_id":"79948","summary":"The proteins in the lipid phosphate phosphatase (LPP) family, including PRG2, are integral membrane proteins that modulate bioactive lipid phosphates including phosphatidate, lysophosphatidate, and sphingosine-1-phosphate in the context of cell migration, neurite retraction, and mitogenesis (Brauer et al., 2003 [PubMed 12730698]).[supplied by OMIM, Mar 2008]","start":812488,"end":821977,"strand":-1,"description":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]"}, {"versioned_ensembl_gene_id":"ENSG00000117335.19","gene_symbol":"CD46","gene_name":"CD46 molecule [Source:HGNC Symbol;Acc:HGNC:6953]","synonyms":"TRA2.10,TLX,MIC10,MGC26544,MCP","biotype":"protein_coding","ncbi_id":"4179","summary":"The protein encoded by this gene is a type I membrane protein and is a regulatory part of the complement system. The encoded protein has cofactor activity for inactivation of complement components C3b and C4b by serum factor I, which protects the host cell from damage by complement. In addition, the encoded protein can act as a receptor for the Edmonston strain of measles virus, human herpesvirus-6, and type IV pili of pathogenic Neisseria. Finally, the protein encoded by this gene may be involved in the fusion of the spermatozoa with the oocyte during fertilization. Mutations at this locus have been associated with susceptibility to hemolytic uremic syndrome. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2010]","start":207752057,"end":207795513,"strand":1,"description":"CD46 molecule [Source:HGNC Symbol;Acc:HGNC:6953]"}, {"versioned_ensembl_gene_id":"ENSG00000196893.3","gene_symbol":"AC090286.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18951625,"end":18954149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211952.3","gene_symbol":"IGHV4-28","gene_name":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28400","summary":null,"start":106324254,"end":106324760,"strand":-1,"description":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]"}, {"versioned_ensembl_gene_id":"ENSG00000249305.1","gene_symbol":"AC048346.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140619694,"end":140619837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253462.1","gene_symbol":"IGHVIII-26-1","gene_name":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]","synonyms":"IGHV(III)-26-1","biotype":"IG_V_pseudogene","ncbi_id":"28347","summary":null,"start":106309417,"end":106309666,"strand":-1,"description":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]"}, {"versioned_ensembl_gene_id":"ENSG00000255421.1","gene_symbol":"AP002340.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76137315,"end":76137731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113318.9","gene_symbol":"MSH3","gene_name":"mutS homolog 3 [Source:HGNC Symbol;Acc:HGNC:7326]","synonyms":"MRP1,DUP","biotype":"protein_coding","ncbi_id":"4437","summary":"The protein encoded by this gene forms a heterodimer with MSH2 to form MutS beta, part of the post-replicative DNA mismatch repair system. MutS beta initiates mismatch repair by binding to a mismatch and then forming a complex with MutL alpha heterodimer. This gene contains a polymorphic 9 bp tandem repeat sequence in the first exon. The repeat is present 6 times in the reference genome sequence and 3-7 repeats have been reported. Defects in this gene are a cause of susceptibility to endometrial cancer. [provided by RefSeq, Mar 2011]","start":80654648,"end":80876460,"strand":1,"description":"mutS homolog 3 [Source:HGNC Symbol;Acc:HGNC:7326]"}, {"versioned_ensembl_gene_id":"ENSG00000259013.2","gene_symbol":"AL118558.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101969364,"end":101969601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116353.15","gene_symbol":"MECR","gene_name":"mitochondrial trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:19691]","synonyms":"NRBF1,FASN2B,ETR1,CGI-63","biotype":"protein_coding","ncbi_id":"51102","summary":"The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]","start":29192873,"end":29230942,"strand":-1,"description":"mitochondrial trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:19691]"}, {"versioned_ensembl_gene_id":"ENSG00000140459.17","gene_symbol":"CYP11A1","gene_name":"cytochrome P450 family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2590]","synonyms":"P450SCC,CYP11A","biotype":"protein_coding","ncbi_id":"1583","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane and catalyzes the conversion of cholesterol to pregnenolone, the first and rate-limiting step in the synthesis of the steroid hormones. Two transcript variants encoding different isoforms have been found for this gene. The cellular location of the smaller isoform is unclear since it lacks the mitochondrial-targeting transit peptide. [provided by RefSeq, Jul 2008]","start":74337759,"end":74367740,"strand":-1,"description":"cytochrome P450 family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2590]"}, {"versioned_ensembl_gene_id":"ENSG00000183644.13","gene_symbol":"C11orf88","gene_name":"chromosome 11 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25061]","synonyms":"FLJ46266","biotype":"protein_coding","ncbi_id":"399949","summary":null,"start":111514785,"end":111537031,"strand":1,"description":"chromosome 11 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25061]"}, {"versioned_ensembl_gene_id":"ENSG00000137707.13","gene_symbol":"BTG4","gene_name":"BTG anti-proliferation factor 4 [Source:HGNC Symbol;Acc:HGNC:13862]","synonyms":"PC3B,APRO3","biotype":"protein_coding","ncbi_id":"54766","summary":"The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein can induce G1 arrest in the cell cycle. [provided by RefSeq, Jul 2008]","start":111467526,"end":111512354,"strand":-1,"description":"BTG anti-proliferation factor 4 [Source:HGNC Symbol;Acc:HGNC:13862]"}, {"versioned_ensembl_gene_id":"ENSG00000178440.5","gene_symbol":"LINC00843","gene_name":"long intergenic non-protein coding RNA 843 [Source:HGNC Symbol;Acc:HGNC:45009]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102902672","summary":null,"start":49972763,"end":49982053,"strand":1,"description":"long intergenic non-protein coding RNA 843 [Source:HGNC Symbol;Acc:HGNC:45009]"}, {"versioned_ensembl_gene_id":"ENSG00000253260.1","gene_symbol":"AC087664.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59561327,"end":59593701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196814.14","gene_symbol":"MVB12B","gene_name":"multivesicular body subunit 12B [Source:HGNC Symbol;Acc:HGNC:23368]","synonyms":"FLJ00001,FAM125B,C9orf28","biotype":"protein_coding","ncbi_id":"89853","summary":"The protein encoded by this gene is a component of the ESCRT-I complex, a heterotetramer, which mediates the sorting of ubiquitinated cargo protein from the plasma membrane to the endosomal vesicle. ESCRT-I complex plays an essential role in HIV budding and endosomal protein sorting. Depletion and overexpression of this and related protein (MVB12A) inhibit HIV-1 infectivity and induce unusual viral assembly defects, indicating a role for MVB12 subunits in regulating ESCRT-mediated virus budding. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":126326849,"end":126507041,"strand":1,"description":"multivesicular body subunit 12B [Source:HGNC Symbol;Acc:HGNC:23368]"}, {"versioned_ensembl_gene_id":"ENSG00000257127.6","gene_symbol":"CLLU1","gene_name":"chronic lymphocytic leukemia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:29841]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574028","summary":"Expression of this gene has been shown to be upregulated in some individuals with chronic lymphocytic leukemia (CLL), and has been used for prognostic and diagnostic purposes. This gene was originally identified as a human-specific putative protein-coding gene due to the presence of a peptide (PAp00140670, HIIYSTFLSK) that could have supported translation at this locus. This peptide is not present in more recent builds of PeptideAtlas, and the presence of a protein product at this locus has not been independently verified. For this reason, this gene is being represented as non-coding. Sequence comparisons to other primates indicates that no other primate is predicted to contain an open reading frame. [provided by RefSeq, Feb 2017]","start":92421531,"end":92431002,"strand":1,"description":"chronic lymphocytic leukemia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:29841]"}, {"versioned_ensembl_gene_id":"ENSG00000249818.1","gene_symbol":"AC097375.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151904932,"end":151928648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158258.16","gene_symbol":"CLSTN2","gene_name":"calsyntenin 2 [Source:HGNC Symbol;Acc:HGNC:17448]","synonyms":"FLJ39113,CSTN2,CS2,CDHR13","biotype":"protein_coding","ncbi_id":"64084","summary":null,"start":139935185,"end":140577397,"strand":1,"description":"calsyntenin 2 [Source:HGNC Symbol;Acc:HGNC:17448]"}, {"versioned_ensembl_gene_id":"ENSG00000232413.1","gene_symbol":"AL589923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126057580,"end":126159613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254215.1","gene_symbol":"IGHVIII-11-1","gene_name":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]","synonyms":"IGHV(III)-11-1","biotype":"IG_V_pseudogene","ncbi_id":"28352","summary":null,"start":106120207,"end":106120473,"strand":-1,"description":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]"}, {"versioned_ensembl_gene_id":"ENSG00000224044.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464469,"end":29469679,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000265246.1","gene_symbol":"AC129926.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27237859,"end":27241661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124191.17","gene_symbol":"TOX2","gene_name":"TOX high mobility group box family member 2 [Source:HGNC Symbol;Acc:HGNC:16095]","synonyms":"C20orf100,GCX-1,dJ1108D11.2","biotype":"protein_coding","ncbi_id":"84969","summary":null,"start":43914864,"end":44069616,"strand":1,"description":"TOX high mobility group box family member 2 [Source:HGNC Symbol;Acc:HGNC:16095]"}, {"versioned_ensembl_gene_id":"ENSG00000282738.1","gene_symbol":"AC243829.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36161607,"end":36162926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144744.16","gene_symbol":"UBA3","gene_name":"ubiquitin like modifier activating enzyme 3 [Source:HGNC Symbol;Acc:HGNC:12470]","synonyms":"UBE1C,NAE2,hUba3","biotype":"protein_coding","ncbi_id":"9039","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E1 ubiquitin-activating enzyme family. The encoded enzyme associates with AppBp1, an amyloid beta precursor protein binding protein, to form a heterodimer, and then the enzyme complex activates NEDD8, a ubiquitin-like protein, which regulates cell division, signaling and embryogenesis. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":69054730,"end":69080408,"strand":-1,"description":"ubiquitin like modifier activating enzyme 3 [Source:HGNC Symbol;Acc:HGNC:12470]"}, {"versioned_ensembl_gene_id":"ENSG00000167912.5","gene_symbol":"AC090152.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59119040,"end":59121346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198846.5","gene_symbol":"TOX","gene_name":"thymocyte selection associated high mobility group box [Source:HGNC Symbol;Acc:HGNC:18988]","synonyms":"TOX1,KIAA0808","biotype":"protein_coding","ncbi_id":"9760","summary":"The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]","start":58805418,"end":59119208,"strand":-1,"description":"thymocyte selection associated high mobility group box [Source:HGNC Symbol;Acc:HGNC:18988]"}, {"versioned_ensembl_gene_id":"ENSG00000256250.1","gene_symbol":"AC073912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130810606,"end":130812438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053254.15","gene_symbol":"FOXN3","gene_name":"forkhead box N3 [Source:HGNC Symbol;Acc:HGNC:1928]","synonyms":"CHES1,C14orf116","biotype":"protein_coding","ncbi_id":"1112","summary":"This gene is a member of the forkhead/winged helix transcription factor family. Checkpoints are eukaryotic DNA damage-inducible cell cycle arrests at G1 and G2. Checkpoint suppressor 1 suppresses multiple yeast checkpoint mutations including mec1, rad9, rad53 and dun1 by activating a MEC1-independent checkpoint pathway. Alternative splicing is observed at the locus, resulting in distinct isoforms. [provided by RefSeq, Jul 2008]","start":89124871,"end":89619149,"strand":-1,"description":"forkhead box N3 [Source:HGNC Symbol;Acc:HGNC:1928]"}, {"versioned_ensembl_gene_id":"ENSG00000259073.1","gene_symbol":"FOXN3-AS2","gene_name":"FOXN3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:30119]","synonyms":"PRO1768","biotype":"antisense_RNA","ncbi_id":"29018","summary":null,"start":89576216,"end":89577477,"strand":1,"description":"FOXN3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:30119]"}, {"versioned_ensembl_gene_id":"ENSG00000123643.12","gene_symbol":"SLC36A1","gene_name":"solute carrier family 36 member 1 [Source:HGNC Symbol;Acc:HGNC:18761]","synonyms":"TRAMD3,PAT1,LYAAT-1","biotype":"protein_coding","ncbi_id":"206358","summary":"This gene encodes a member of the eukaryote-specific amino acid/auxin permease (AAAP) 1 transporter family. The encoded protein functions as a proton-dependent, small amino acid transporter. This gene is clustered with related family members on chromosome 5q33.1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":151437046,"end":151492381,"strand":1,"description":"solute carrier family 36 member 1 [Source:HGNC Symbol;Acc:HGNC:18761]"}, {"versioned_ensembl_gene_id":"ENSG00000211933.2","gene_symbol":"IGHV6-1","gene_name":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28385","summary":null,"start":105939756,"end":105940253,"strand":-1,"description":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]"}, {"versioned_ensembl_gene_id":"ENSG00000257065.1","gene_symbol":"AL049844.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":143807092,"end":143844617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021852.12","gene_symbol":"C8B","gene_name":"complement C8 beta chain [Source:HGNC Symbol;Acc:HGNC:1353]","synonyms":null,"biotype":"protein_coding","ncbi_id":"732","summary":"This gene encodes one of the three subunits of the complement component 8 (C8) protein. C8 is composed of equimolar amounts of alpha, beta and gamma subunits, which are encoded by three separate genes. C8 is one component of the membrane attack complex, which mediates cell lysis, and it initiates membrane penetration of the complex. This protein mediates the interaction of C8 with the C5b-7 membrane attack complex precursor. In humans deficiency of this protein is associated with increased risk of meningococcal infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":56929210,"end":56966140,"strand":-1,"description":"complement C8 beta chain [Source:HGNC Symbol;Acc:HGNC:1353]"}, {"versioned_ensembl_gene_id":"ENSG00000236170.1","gene_symbol":"IGHD1-1","gene_name":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]","synonyms":"IGHD11","biotype":"IG_D_gene","ncbi_id":"28510","summary":null,"start":105919502,"end":105919518,"strand":-1,"description":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]"}, {"versioned_ensembl_gene_id":"ENSG00000226777.7","gene_symbol":"FAM30A","gene_name":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]","synonyms":"KIAA0125,HSPC053,C14orf110","biotype":"lincRNA","ncbi_id":"9834","summary":null,"start":105917979,"end":105932642,"strand":1,"description":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]"}, {"versioned_ensembl_gene_id":"ENSG00000255280.1","gene_symbol":"AP001922.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75642600,"end":75642889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270371.1","gene_symbol":"AL122127.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105785505,"end":105785831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254298.1","gene_symbol":"AC008641.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151158106,"end":151158462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244413.1","gene_symbol":"RPL23AP56","gene_name":"ribosomal protein L23a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35516]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645809","summary":null,"start":134978827,"end":134979279,"strand":-1,"description":"ribosomal protein L23a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35516]"}, {"versioned_ensembl_gene_id":"ENSG00000236626.1","gene_symbol":"MTND5P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42279]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873353","summary":null,"start":36432882,"end":36434484,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42279]"}, {"versioned_ensembl_gene_id":"ENSG00000187486.5","gene_symbol":"KCNJ11","gene_name":"potassium voltage-gated channel subfamily J member 11 [Source:HGNC Symbol;Acc:HGNC:6257]","synonyms":"Kir6.2,BIR","biotype":"protein_coding","ncbi_id":"3767","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2009]","start":17385859,"end":17389331,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 11 [Source:HGNC Symbol;Acc:HGNC:6257]"}, {"versioned_ensembl_gene_id":"ENSG00000261432.1","gene_symbol":"LINC01613","gene_name":"long intergenic non-protein coding RNA 1613 [Source:HGNC Symbol;Acc:HGNC:51842]","synonyms":"n341773","biotype":"lincRNA","ncbi_id":"106146149","summary":null,"start":119935053,"end":119937832,"strand":1,"description":"long intergenic non-protein coding RNA 1613 [Source:HGNC Symbol;Acc:HGNC:51842]"}, {"versioned_ensembl_gene_id":"ENSG00000278954.1","gene_symbol":"AC130686.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41665566,"end":41668031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268238.1","gene_symbol":"IGFL1P2","gene_name":"IGF like family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32957]","synonyms":"IGFL-6P","biotype":"unprocessed_pseudogene","ncbi_id":"727704","summary":null,"start":46260420,"end":46260858,"strand":-1,"description":"IGF like family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32957]"}, {"versioned_ensembl_gene_id":"ENSG00000155087.3","gene_symbol":"ODF1","gene_name":"outer dense fiber of sperm tails 1 [Source:HGNC Symbol;Acc:HGNC:8113]","synonyms":"CT133,RT7,ODFPG,ODF27,HSPB10","biotype":"protein_coding","ncbi_id":"4956","summary":"The outer dense fibers are cytoskeletal structures that surround the axoneme in the middle piece and principal piece of the sperm tail. The fibers function in maintaining the elastic structure and recoil of the sperm tail as well as in protecting the tail from shear forces during epididymal transport and ejaculation. Defects in the outer dense fibers lead to abnormal sperm morphology and infertility. The human outer dense fibers contains at least 10 major proteins and this gene encodes the main protein. [provided by RefSeq, Jul 2008]","start":102551572,"end":102561017,"strand":1,"description":"outer dense fiber of sperm tails 1 [Source:HGNC Symbol;Acc:HGNC:8113]"}, {"versioned_ensembl_gene_id":"ENSG00000249602.1","gene_symbol":"AL589765.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151763384,"end":151769501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203288.3","gene_symbol":"TDRKH-AS1","gene_name":"TDRKH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40578]","synonyms":"RP11-98D18.9","biotype":"antisense_RNA","ncbi_id":"109729141","summary":null,"start":151790804,"end":151794402,"strand":1,"description":"TDRKH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40578]"}, {"versioned_ensembl_gene_id":"ENSG00000100284.20","gene_symbol":"TOM1","gene_name":"target of myb1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11982]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10043","summary":"This gene was identified as a target of the v-myb oncogene. The encoded protein shares its N-terminal domain in common with proteins associated with vesicular trafficking at the endosome. It is recruited to the endosomes by its interaction with endofin. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":35299275,"end":35347994,"strand":1,"description":"target of myb1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11982]"}, {"versioned_ensembl_gene_id":"ENSG00000237273.1","gene_symbol":"RSL24D1P8","gene_name":"ribosomal L24 domain containing 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37873]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462809","summary":null,"start":12096424,"end":12096915,"strand":1,"description":"ribosomal L24 domain containing 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37873]"}, {"versioned_ensembl_gene_id":"ENSG00000239269.1","gene_symbol":"RPSAP4","gene_name":"ribosomal protein SA pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:20018]","synonyms":"LAMR1P4","biotype":"processed_pseudogene","ncbi_id":"145259","summary":null,"start":94726288,"end":94727175,"strand":1,"description":"ribosomal protein SA pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:20018]"}, {"versioned_ensembl_gene_id":"ENSG00000268916.6","gene_symbol":"CSAG3","gene_name":"CSAG family member 3 [Source:HGNC Symbol;Acc:HGNC:26237]","synonyms":"CSAG3A","biotype":"protein_coding","ncbi_id":"389903","summary":null,"start":152753921,"end":152760222,"strand":1,"description":"CSAG family member 3 [Source:HGNC Symbol;Acc:HGNC:26237]"}, {"versioned_ensembl_gene_id":"ENSG00000214827.9","gene_symbol":"MTCP1","gene_name":"mature T-cell proliferation 1 [Source:HGNC Symbol;Acc:HGNC:7423]","synonyms":"p8MTCP1,P13MTCP1","biotype":"protein_coding","ncbi_id":"4515","summary":"This gene was identified by involvement in some t(X;14) translocations associated with mature T-cell proliferations. This region has a complex gene structure, with a common promoter and 5' exon spliced to two different sets of 3' exons that encode two different proteins. This gene represents the upstream 13 kDa protein that is a member of the TCL1 family. This protein may be involved in leukemogenesis. [provided by RefSeq, Mar 2009]","start":155061622,"end":155147937,"strand":-1,"description":"mature T-cell proliferation 1 [Source:HGNC Symbol;Acc:HGNC:7423]"}, {"versioned_ensembl_gene_id":"ENSG00000160803.7","gene_symbol":"UBQLN4","gene_name":"ubiquilin 4 [Source:HGNC Symbol;Acc:HGNC:1237]","synonyms":"A1U,UBIN,C1orf6","biotype":"protein_coding","ncbi_id":"56893","summary":null,"start":156035301,"end":156053794,"strand":-1,"description":"ubiquilin 4 [Source:HGNC Symbol;Acc:HGNC:1237]"}, {"versioned_ensembl_gene_id":"ENSG00000186020.12","gene_symbol":"ZNF529","gene_name":"zinc finger protein 529 [Source:HGNC Symbol;Acc:HGNC:29328]","synonyms":"KIAA1615","biotype":"protein_coding","ncbi_id":"57711","summary":null,"start":36534774,"end":36605276,"strand":-1,"description":"zinc finger protein 529 [Source:HGNC Symbol;Acc:HGNC:29328]"}, {"versioned_ensembl_gene_id":"ENSG00000075914.12","gene_symbol":"EXOSC7","gene_name":"exosome component 7 [Source:HGNC Symbol;Acc:HGNC:28112]","synonyms":"hRrp42p,EAP1,Rrp42p,RRP42,p8,KIAA0116","biotype":"protein_coding","ncbi_id":"23016","summary":null,"start":44975241,"end":45036066,"strand":1,"description":"exosome component 7 [Source:HGNC Symbol;Acc:HGNC:28112]"}, {"versioned_ensembl_gene_id":"ENSG00000233646.1","gene_symbol":"OR52T1P","gene_name":"olfactory receptor family 52 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15236]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81244","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5566678,"end":5567616,"strand":-1,"description":"olfactory receptor family 52 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15236]"}, {"versioned_ensembl_gene_id":"ENSG00000268288.1","gene_symbol":"AL589765.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151766486,"end":151767000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258659.6","gene_symbol":"TRIM34","gene_name":"tripartite motif containing 34 [Source:HGNC Symbol;Acc:HGNC:10063]","synonyms":"RNF21","biotype":"protein_coding","ncbi_id":"53840","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, B-box type 1 and B-box type 2 domain, and a coiled-coil region. Expression of this gene is up-regulated by interferon. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. Alternative splicing results in multiple transcript variants. A read-through transcript from the upstream TRIM6 gene has also been observed, which results in a fusion product from these neighboring family members. [provided by RefSeq, Oct 2010]","start":5619764,"end":5644398,"strand":1,"description":"tripartite motif containing 34 [Source:HGNC Symbol;Acc:HGNC:10063]"}, {"versioned_ensembl_gene_id":"ENSG00000229704.1","gene_symbol":"EIF2S2P2","gene_name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24654]","synonyms":"bcm2636","biotype":"processed_pseudogene","ncbi_id":"347673","summary":null,"start":185245460,"end":185246441,"strand":-1,"description":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24654]"}, {"versioned_ensembl_gene_id":"ENSG00000278339.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755024,"end":54767369,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000239600.1","gene_symbol":"AP000797.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115951105,"end":115951491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167083.6","gene_symbol":"GNGT2","gene_name":"G protein subunit gamma transducin 2 [Source:HGNC Symbol;Acc:HGNC:4412]","synonyms":"GNG9","biotype":"protein_coding","ncbi_id":"2793","summary":"Phototransduction in rod and cone photoreceptors is regulated by groups of signaling proteins. The encoded protein is thought to play a crucial role in cone phototransduction. It belongs to the G protein gamma family and localized specifically in cones. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2010]","start":49202791,"end":49210574,"strand":-1,"description":"G protein subunit gamma transducin 2 [Source:HGNC Symbol;Acc:HGNC:4412]"}, {"versioned_ensembl_gene_id":"ENSG00000162885.12","gene_symbol":"B3GALNT2","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]","synonyms":"MGC39558","biotype":"protein_coding","ncbi_id":"148789","summary":"This gene encodes a member of the glycosyltransferase 31 family. The encoded protein synthesizes GalNAc:beta-1,3GlcNAc, a novel carbohydrate structure, on N- and O-glycans. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2013]","start":235449923,"end":235504481,"strand":-1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]"}, {"versioned_ensembl_gene_id":"ENSG00000279818.1","gene_symbol":"AP002991.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":115731942,"end":115734742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178243.4","gene_symbol":"C9orf62","gene_name":"chromosome 9 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28581]","synonyms":"MGC35463","biotype":"lincRNA","ncbi_id":"157927","summary":null,"start":135343249,"end":135346562,"strand":1,"description":"chromosome 9 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28581]"}, {"versioned_ensembl_gene_id":"ENSG00000146001.5","gene_symbol":"PCDHB18P","gene_name":"protocadherin beta 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:14548]","synonyms":"PCDHB18,PCDH-psi2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54660","summary":null,"start":141234333,"end":141237529,"strand":1,"description":"protocadherin beta 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:14548]"}, {"versioned_ensembl_gene_id":"ENSG00000250719.1","gene_symbol":"AL672043.1","gene_name":"Homo sapiens uncharacterized LOC110117498 (LOC110117498), mRNA. [Source:RefSeq mRNA;Acc:NM_001328655]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46175486,"end":46176478,"strand":-1,"description":"Homo sapiens uncharacterized LOC110117498 (LOC110117498), mRNA. [Source:RefSeq mRNA;Acc:NM_001328655]"}, {"versioned_ensembl_gene_id":"ENSG00000273736.1","gene_symbol":"AC244100.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35963488,"end":35965472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214514.7","gene_symbol":"KRT42P","gene_name":"keratin 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:27581]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284116","summary":null,"start":41626327,"end":41640199,"strand":-1,"description":"keratin 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:27581]"}, {"versioned_ensembl_gene_id":"ENSG00000226957.1","gene_symbol":"AL358075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46046818,"end":46048368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260136.5","gene_symbol":"AC008915.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23452758,"end":23457606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160284.14","gene_symbol":"SPATC1L","gene_name":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]","synonyms":"C21orf56","biotype":"protein_coding","ncbi_id":"84221","summary":null,"start":46161148,"end":46184476,"strand":-1,"description":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]"}, {"versioned_ensembl_gene_id":"ENSG00000280039.1","gene_symbol":"RN7SKP23","gene_name":"RNA, 7SK small nuclear pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:45747]","synonyms":null,"biotype":"TEC","ncbi_id":"106479105","summary":null,"start":23412380,"end":23416680,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:45747]"}, {"versioned_ensembl_gene_id":"ENSG00000259782.2","gene_symbol":"AC008915.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":23446446,"end":23447282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117461.14","gene_symbol":"PIK3R3","gene_name":"phosphoinositide-3-kinase regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:8981]","synonyms":"p55","biotype":"protein_coding","ncbi_id":"8503","summary":"Phosphatidylinositol 3-kinase (PI3K) phosphorylates phosphatidylinositol and similar compounds, which then serve as second messengers in growth signaling pathways. PI3K is composed of a catalytic and a regulatory subunit. The protein encoded by this gene represents a regulatory subunit of PI3K. The encoded protein contains two SH2 domains through which it binds activated protein tyrosine kinases to regulate their activity. [provided by RefSeq, Jun 2016]","start":46040140,"end":46133036,"strand":-1,"description":"phosphoinositide-3-kinase regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:8981]"}, {"versioned_ensembl_gene_id":"ENSG00000279047.3","gene_symbol":"AC244517.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141046260,"end":141096402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197149.5","gene_symbol":"AC107956.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17228279,"end":17229151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104967.6","gene_symbol":"NOVA2","gene_name":"NOVA alternative splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:7887]","synonyms":"NOVA3,ANOVA","biotype":"protein_coding","ncbi_id":"4858","summary":null,"start":45933734,"end":45973546,"strand":-1,"description":"NOVA alternative splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:7887]"}, {"versioned_ensembl_gene_id":"ENSG00000277539.1","gene_symbol":"AC138058.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71276087,"end":71289616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229732.1","gene_symbol":"AC019349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41500983,"end":41502409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223609.7","gene_symbol":"HBD","gene_name":"hemoglobin subunit delta [Source:HGNC Symbol;Acc:HGNC:4829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3045","summary":"The delta (HBD) and beta (HBB) genes are normally expressed in the adult: two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin. Two alpha chains plus two delta chains constitute HbA-2, which with HbF comprises the remaining 3% of adult hemoglobin. Five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon--Ggamma--Agamma--delta--beta-3'. Mutations in the delta-globin gene are associated with beta-thalassemia. [provided by RefSeq, Jul 2008]","start":5232678,"end":5235370,"strand":-1,"description":"hemoglobin subunit delta [Source:HGNC Symbol;Acc:HGNC:4829]"}, {"versioned_ensembl_gene_id":"ENSG00000099617.3","gene_symbol":"EFNA2","gene_name":"ephrin A2 [Source:HGNC Symbol;Acc:HGNC:3222]","synonyms":"LERK6,EPLG6,ELF-1","biotype":"protein_coding","ncbi_id":"1943","summary":"This gene encodes a member of the ephrin family. The protein is composed of a signal sequence, a receptor-binding region, a spacer region, and a hydrophobic region. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. Posttranslational modifications determine whether this protein localizes to the nucleus or the cytoplasm. [provided by RefSeq, Jul 2008]","start":1286154,"end":1300237,"strand":1,"description":"ephrin A2 [Source:HGNC Symbol;Acc:HGNC:3222]"}, {"versioned_ensembl_gene_id":"ENSG00000229992.1","gene_symbol":"HMGB3P9","gene_name":"high mobility group box 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873879","summary":null,"start":92647048,"end":92647630,"strand":-1,"description":"high mobility group box 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39301]"}, {"versioned_ensembl_gene_id":"ENSG00000254629.1","gene_symbol":"AP002370.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83789977,"end":83791578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266973.1","gene_symbol":"AC092296.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36378028,"end":36378832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235924.1","gene_symbol":"ZNRF2P3","gene_name":"zinc and ring finger 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45113]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130879","summary":null,"start":79981839,"end":79982212,"strand":1,"description":"zinc and ring finger 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45113]"}, {"versioned_ensembl_gene_id":"ENSG00000276868.1","gene_symbol":"AL353626.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40883634,"end":40883763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249778.1","gene_symbol":"TRMT112P2","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479033","summary":null,"start":80033171,"end":80033302,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44021]"}, {"versioned_ensembl_gene_id":"ENSG00000235220.10","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29720256,"end":29736008,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000240871.5","gene_symbol":"KRTAP4-7","gene_name":"keratin associated protein 4-7 [Source:HGNC Symbol;Acc:HGNC:18898]","synonyms":"KAP4.7","biotype":"protein_coding","ncbi_id":"100132476","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Mar 2009]","start":41084150,"end":41085141,"strand":1,"description":"keratin associated protein 4-7 [Source:HGNC Symbol;Acc:HGNC:18898]"}, {"versioned_ensembl_gene_id":"ENSG00000236838.2","gene_symbol":"AC090617.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2213697,"end":2214414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275386.1","gene_symbol":"AC105081.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":93974671,"end":93974776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255037.1","gene_symbol":"AC136443.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14766402,"end":14770075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198496.10","gene_symbol":"NBR2","gene_name":"neighbor of BRCA1 gene 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20691]","synonyms":"NCRNA00192","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10230","summary":"This gene was identified by its close proximity on chromosome 17 to tumor suppressor gene BRCA1. Experimental evidence indicates that the two genes share a bi-directional promoter. Transcription for either gene is controlled individually by distinct transcriptional repressor factors. A short (112 amino acid) open reading frame is observed which includes a region derived from a LINE1 element. A strong Kozak signal is not observed for the putative ORF and the stop codon is more than 55 nucleotides upstream of the last splice site for the transcript, suggesting that the transcript is subject to nonsense-mediated decay. Therefore, this gene does not appear to encode a protein. Glucose starvation induces the expression of this gene and the long non-coding RNA transcribed by it functions with AMP-activated protein kinase in mediating the energy stress response. [provided by RefSeq, Aug 2016]","start":43125610,"end":43153671,"strand":1,"description":"neighbor of BRCA1 gene 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20691]"}, {"versioned_ensembl_gene_id":"ENSG00000255341.1","gene_symbol":"OR8Q1P","gene_name":"olfactory receptor family 8 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15317]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81163","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124601584,"end":124602238,"strand":1,"description":"olfactory receptor family 8 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15317]"}, {"versioned_ensembl_gene_id":"ENSG00000274473.2","gene_symbol":"SCT","gene_name":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6343","summary":"This gene encodes a member of the glucagon family of peptides. The encoded preproprotein is secreted by endocrine S cells in the proximal small intestinal mucosa as a prohormone, then proteolytically processed to generate the mature peptide hormone. The release of this active peptide hormone is stimulated by either fatty acids or acidic pH in the duodenum. This hormone stimulates the secretion of bile and bicarbonate in the duodenum, pancreatic and biliary ducts. [provided by RefSeq, Feb 2016]","start":626689,"end":627401,"strand":-1,"description":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]"}, {"versioned_ensembl_gene_id":"ENSG00000223604.1","gene_symbol":"AC007394.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149439897,"end":149440427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175329.12","gene_symbol":"ISX","gene_name":"intestine specific homeobox [Source:HGNC Symbol;Acc:HGNC:28084]","synonyms":"RAXLX","biotype":"protein_coding","ncbi_id":"91464","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the RAXLX homeobox gene family. [provided by RefSeq, Jul 2008]","start":35066136,"end":35087387,"strand":1,"description":"intestine specific homeobox [Source:HGNC Symbol;Acc:HGNC:28084]"}, {"versioned_ensembl_gene_id":"ENSG00000236237.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31656860,"end":31658827,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000253852.1","gene_symbol":"AC011383.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150608428,"end":150615354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165868.13","gene_symbol":"HSPA12A","gene_name":"heat shock protein family A (Hsp70) member 12A [Source:HGNC Symbol;Acc:HGNC:19022]","synonyms":"KIAA0417,FLJ13874","biotype":"protein_coding","ncbi_id":"259217","summary":null,"start":116671192,"end":116849741,"strand":-1,"description":"heat shock protein family A (Hsp70) member 12A [Source:HGNC Symbol;Acc:HGNC:19022]"}, {"versioned_ensembl_gene_id":"ENSG00000237544.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29475501,"end":29476547,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000276896.4","gene_symbol":"GOLGA8F","gene_name":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]","synonyms":"DKFZp434P162","biotype":"protein_coding","ncbi_id":"100132565","summary":null,"start":28378587,"end":28391990,"strand":1,"description":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]"}, {"versioned_ensembl_gene_id":"ENSG00000152422.15","gene_symbol":"XRCC4","gene_name":"X-ray repair cross complementing 4 [Source:HGNC Symbol;Acc:HGNC:12831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7518","summary":"The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site. [provided by RefSeq, Oct 2019]","start":83077498,"end":83353787,"strand":1,"description":"X-ray repair cross complementing 4 [Source:HGNC Symbol;Acc:HGNC:12831]"}, {"versioned_ensembl_gene_id":"ENSG00000259803.6","gene_symbol":"SLC22A31","gene_name":"solute carrier family 22 member 31 [Source:HGNC Symbol;Acc:HGNC:27091]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146429","summary":null,"start":89195761,"end":89201664,"strand":-1,"description":"solute carrier family 22 member 31 [Source:HGNC Symbol;Acc:HGNC:27091]"}, {"versioned_ensembl_gene_id":"ENSG00000280333.1","gene_symbol":"AC090617.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2072823,"end":2072956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248807.1","gene_symbol":"KRTAP9-12P","gene_name":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287715","summary":null,"start":41212706,"end":41213237,"strand":1,"description":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]"}, {"versioned_ensembl_gene_id":"ENSG00000280051.1","gene_symbol":"AC079456.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":129262345,"end":129262824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160325.14","gene_symbol":"CACFD1","gene_name":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]","synonyms":"flower,D9S2135,C9orf7","biotype":"protein_coding","ncbi_id":"11094","summary":null,"start":133459965,"end":133470848,"strand":1,"description":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]"}, {"versioned_ensembl_gene_id":"ENSG00000256699.1","gene_symbol":"TMEM132D-AS2","gene_name":"TMEM132D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53324]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927735","summary":null,"start":129208601,"end":129212662,"strand":1,"description":"TMEM132D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53324]"}, {"versioned_ensembl_gene_id":"ENSG00000258673.1","gene_symbol":"LINC01397","gene_name":"long intergenic non-protein coding RNA 1397 [Source:HGNC Symbol;Acc:HGNC:50677]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355139","summary":null,"start":110082688,"end":110109719,"strand":1,"description":"long intergenic non-protein coding RNA 1397 [Source:HGNC Symbol;Acc:HGNC:50677]"}, {"versioned_ensembl_gene_id":"ENSG00000215883.10","gene_symbol":"CYB5RL","gene_name":"cytochrome b5 reductase like [Source:HGNC Symbol;Acc:HGNC:32220]","synonyms":"LOC606495","biotype":"protein_coding","ncbi_id":"606495","summary":null,"start":54169651,"end":54200036,"strand":-1,"description":"cytochrome b5 reductase like [Source:HGNC Symbol;Acc:HGNC:32220]"}, {"versioned_ensembl_gene_id":"ENSG00000135083.14","gene_symbol":"CCNJL","gene_name":"cyclin J like [Source:HGNC Symbol;Acc:HGNC:25876]","synonyms":"FLJ14166","biotype":"protein_coding","ncbi_id":"79616","summary":null,"start":160251652,"end":160345396,"strand":-1,"description":"cyclin J like [Source:HGNC Symbol;Acc:HGNC:25876]"}, {"versioned_ensembl_gene_id":"ENSG00000140691.16","gene_symbol":"ARMC5","gene_name":"armadillo repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:25781]","synonyms":"FLJ13063","biotype":"protein_coding","ncbi_id":"79798","summary":"This gene encodes a member of the ARM (armadillo/beta-catenin-like repeat) superfamily. The ARM repeat is a tandemly repeated sequence motif with approximately 40 amino acid long. This repeat is implicated in mediating protein-protein interactions. The encoded protein contains seven ARM repeats. Mutations in this gene are associated with primary bilateral macronodular adrenal hyperplasia, which is also known as ACTH-independent macronodular adrenal hyperplasia 2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":31458080,"end":31467166,"strand":1,"description":"armadillo repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:25781]"}, {"versioned_ensembl_gene_id":"ENSG00000250821.2","gene_symbol":"EXOC1L","gene_name":"exocyst complex component 1 like [Source:HGNC Symbol;Acc:HGNC:53433]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644145","summary":null,"start":55819819,"end":55837487,"strand":1,"description":"exocyst complex component 1 like [Source:HGNC Symbol;Acc:HGNC:53433]"}, {"versioned_ensembl_gene_id":"ENSG00000256407.2","gene_symbol":"AL357673.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54132686,"end":54200073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242067.1","gene_symbol":"AC091179.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48691116,"end":48691694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171014.2","gene_symbol":"OR4D5","gene_name":"olfactory receptor family 4 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:14852]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219875","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123939543,"end":123940637,"strand":1,"description":"olfactory receptor family 4 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:14852]"}, {"versioned_ensembl_gene_id":"ENSG00000141298.17","gene_symbol":"SSH2","gene_name":"slingshot protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:30580]","synonyms":"KIAA1725","biotype":"protein_coding","ncbi_id":"85464","summary":"This gene encodes a protein tyrosine phosphatase that plays a key role in the regulation of actin filaments. The encoded protein dephosphorylates and activates cofilin, which promotes actin filament depolymerization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":29625938,"end":29930276,"strand":-1,"description":"slingshot protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:30580]"}, {"versioned_ensembl_gene_id":"ENSG00000229388.1","gene_symbol":"LINC01715","gene_name":"long intergenic non-protein coding RNA 1715 [Source:HGNC Symbol;Acc:HGNC:52502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378616","summary":null,"start":28643228,"end":28648581,"strand":1,"description":"long intergenic non-protein coding RNA 1715 [Source:HGNC Symbol;Acc:HGNC:52502]"}, {"versioned_ensembl_gene_id":"ENSG00000263063.1","gene_symbol":"AC024361.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82713908,"end":82716255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264985.2","gene_symbol":"AC124804.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73513612,"end":73521407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233271.1","gene_symbol":"AL590440.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54980950,"end":54992274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143001.4","gene_symbol":"TMEM61","gene_name":"transmembrane protein 61 [Source:HGNC Symbol;Acc:HGNC:27296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"199964","summary":null,"start":54980792,"end":54992293,"strand":1,"description":"transmembrane protein 61 [Source:HGNC Symbol;Acc:HGNC:27296]"}, {"versioned_ensembl_gene_id":"ENSG00000231536.1","gene_symbol":"AC226101.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110610916,"end":110612404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216867.2","gene_symbol":"AC226101.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110633947,"end":110634333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242396.1","gene_symbol":"AC096536.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54886875,"end":54888001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226186.1","gene_symbol":"ELOCP21","gene_name":"elongin C pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38157]","synonyms":"TCEB1P21","biotype":"processed_pseudogene","ncbi_id":"100462866","summary":null,"start":70955899,"end":70956234,"strand":-1,"description":"elongin C pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38157]"}, {"versioned_ensembl_gene_id":"ENSG00000235072.2","gene_symbol":"AC012074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25369136,"end":25375845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258881.6","gene_symbol":"AC007040.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":70939318,"end":70995336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255408.3","gene_symbol":"PCDHA3","gene_name":"protocadherin alpha 3 [Source:HGNC Symbol;Acc:HGNC:8669]","synonyms":"PCDH-ALPHA3","biotype":"protein_coding","ncbi_id":"56145","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140801028,"end":141012344,"strand":1,"description":"protocadherin alpha 3 [Source:HGNC Symbol;Acc:HGNC:8669]"}, {"versioned_ensembl_gene_id":"ENSG00000229273.1","gene_symbol":"BX664615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39809562,"end":39810019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233719.4","gene_symbol":"GOT2P3","gene_name":"glutamic-oxaloacetic transaminase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4436]","synonyms":"GOT2L3P,GOT2L3","biotype":"transcribed_processed_pseudogene","ncbi_id":"644138","summary":null,"start":9641723,"end":9643011,"strand":1,"description":"glutamic-oxaloacetic transaminase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4436]"}, {"versioned_ensembl_gene_id":"ENSG00000273994.1","gene_symbol":"SDR42E1P1","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422340","summary":null,"start":39651901,"end":39652377,"strand":-1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50378]"}, {"versioned_ensembl_gene_id":"ENSG00000229707.1","gene_symbol":"SKP1P3","gene_name":"S-phase kinase associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101119","summary":null,"start":39485379,"end":39485865,"strand":1,"description":"S-phase kinase associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50370]"}, {"versioned_ensembl_gene_id":"ENSG00000160323.18","gene_symbol":"ADAMTS13","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]","synonyms":"FLJ42993,VWFCP,DKFZp434C2322,vWF-CP,C9orf8,TTP,MGC118900,MGC118899","biotype":"protein_coding","ncbi_id":"11093","summary":"This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133414358,"end":133459402,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]"}, {"versioned_ensembl_gene_id":"ENSG00000100234.11","gene_symbol":"TIMP3","gene_name":"TIMP metallopeptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:11822]","synonyms":"SFD","biotype":"protein_coding","ncbi_id":"7078","summary":"This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy. [provided by RefSeq, Jul 2008]","start":32801701,"end":32863043,"strand":1,"description":"TIMP metallopeptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:11822]"}, {"versioned_ensembl_gene_id":"ENSG00000198554.11","gene_symbol":"WDHD1","gene_name":"WD repeat and HMG-box DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23170]","synonyms":"CHTF4,AND-1,CTF4","biotype":"protein_coding","ncbi_id":"11169","summary":"The protein encoded by this gene contains multiple N-terminal WD40 domains and a C-terminal high mobility group (HMG) box. WD40 domains are found in a variety of eukaryotic proteins and may function as adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54938950,"end":55027105,"strand":-1,"description":"WD repeat and HMG-box DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23170]"}, {"versioned_ensembl_gene_id":"ENSG00000204444.10","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"NG20,G3a,ApoM","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31652416,"end":31658210,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000254986.7","gene_symbol":"DPP3","gene_name":"dipeptidyl peptidase 3 [Source:HGNC Symbol;Acc:HGNC:3008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10072","summary":"This gene encodes a protein that is a member of the M49 family of metallopeptidases. This cytoplasmic protein binds a single zinc ion with its zinc-binding motif (HELLGH) and has post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Increased activity of this protein is associated with endometrial and ovarian cancers. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2012]","start":66480013,"end":66509657,"strand":1,"description":"dipeptidyl peptidase 3 [Source:HGNC Symbol;Acc:HGNC:3008]"}, {"versioned_ensembl_gene_id":"ENSG00000189144.13","gene_symbol":"ZNF573","gene_name":"zinc finger protein 573 [Source:HGNC Symbol;Acc:HGNC:26420]","synonyms":"FLJ30921","biotype":"protein_coding","ncbi_id":"126231","summary":null,"start":37735833,"end":37817300,"strand":-1,"description":"zinc finger protein 573 [Source:HGNC Symbol;Acc:HGNC:26420]"}, {"versioned_ensembl_gene_id":"ENSG00000229696.1","gene_symbol":"KARSP1","gene_name":"lysyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39207]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419558","summary":null,"start":41925598,"end":41927349,"strand":1,"description":"lysyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39207]"}, {"versioned_ensembl_gene_id":"ENSG00000137818.11","gene_symbol":"RPLP1","gene_name":"ribosomal protein lateral stalk subunit P1 [Source:HGNC Symbol;Acc:HGNC:10372]","synonyms":"LP1","biotype":"protein_coding","ncbi_id":"6176","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P2. The P1 protein can interact with P0 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Two alternatively spliced transcript variants that encode different proteins have been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":69452784,"end":69456194,"strand":1,"description":"ribosomal protein lateral stalk subunit P1 [Source:HGNC Symbol;Acc:HGNC:10372]"}, {"versioned_ensembl_gene_id":"ENSG00000160447.6","gene_symbol":"PKN3","gene_name":"protein kinase N3 [Source:HGNC Symbol;Acc:HGNC:17999]","synonyms":"UTDP4-1,PKNbeta","biotype":"protein_coding","ncbi_id":"29941","summary":null,"start":128702523,"end":128720918,"strand":1,"description":"protein kinase N3 [Source:HGNC Symbol;Acc:HGNC:17999]"}, {"versioned_ensembl_gene_id":"ENSG00000229954.1","gene_symbol":"MTND2P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"56168","summary":null,"start":102786813,"end":102788387,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23767]"}, {"versioned_ensembl_gene_id":"ENSG00000224471.2","gene_symbol":"MTCO3P19","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52049]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075156","summary":null,"start":102799563,"end":102799883,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52049]"}, {"versioned_ensembl_gene_id":"ENSG00000158234.12","gene_symbol":"FAIM","gene_name":"Fas apoptotic inhibitory molecule [Source:HGNC Symbol;Acc:HGNC:18703]","synonyms":"FLJ10582,FAIM1","biotype":"protein_coding","ncbi_id":"55179","summary":"The protein encoded by this gene protects against death receptor-triggered apoptosis and regulates B-cell signaling and differentiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":138608606,"end":138633376,"strand":1,"description":"Fas apoptotic inhibitory molecule [Source:HGNC Symbol;Acc:HGNC:18703]"}, {"versioned_ensembl_gene_id":"ENSG00000185666.14","gene_symbol":"SYN3","gene_name":"synapsin III [Source:HGNC Symbol;Acc:HGNC:11496]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8224","summary":"This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq, Oct 2008]","start":32512552,"end":33058372,"strand":-1,"description":"synapsin III [Source:HGNC Symbol;Acc:HGNC:11496]"}, {"versioned_ensembl_gene_id":"ENSG00000261379.1","gene_symbol":"AC010735.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":226804036,"end":226805061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087074.7","gene_symbol":"PPP1R15A","gene_name":"protein phosphatase 1 regulatory subunit 15A [Source:HGNC Symbol;Acc:HGNC:14375]","synonyms":"GADD34","biotype":"protein_coding","ncbi_id":"23645","summary":"This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status, and its protein response is correlated with apoptosis following ionizing radiation. [provided by RefSeq, Jul 2008]","start":48872392,"end":48876057,"strand":1,"description":"protein phosphatase 1 regulatory subunit 15A [Source:HGNC Symbol;Acc:HGNC:14375]"}, {"versioned_ensembl_gene_id":"ENSG00000256349.1","gene_symbol":"AP002748.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66509079,"end":66533613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219430.2","gene_symbol":"MBL3P","gene_name":"mannose-binding lectin family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2221]","synonyms":"MBL,COLEC2","biotype":"unprocessed_pseudogene","ncbi_id":"50639","summary":null,"start":79582298,"end":79584877,"strand":-1,"description":"mannose-binding lectin family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2221]"}, {"versioned_ensembl_gene_id":"ENSG00000189190.9","gene_symbol":"ZNF600","gene_name":"zinc finger protein 600 [Source:HGNC Symbol;Acc:HGNC:30951]","synonyms":"KR-ZNF1,DKFZp686F06123","biotype":"protein_coding","ncbi_id":"162966","summary":null,"start":52764195,"end":52786791,"strand":-1,"description":"zinc finger protein 600 [Source:HGNC Symbol;Acc:HGNC:30951]"}, {"versioned_ensembl_gene_id":"ENSG00000264734.1","gene_symbol":"AC069061.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26989189,"end":26999941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225401.2","gene_symbol":"TGIF2P1","gene_name":"TGFB induced factor homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33317]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126826","summary":null,"start":244394976,"end":244395660,"strand":-1,"description":"TGFB induced factor homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33317]"}, {"versioned_ensembl_gene_id":"ENSG00000278980.1","gene_symbol":"AP003485.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91208838,"end":91209590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237693.4","gene_symbol":"IRGM","gene_name":"immunity related GTPase M [Source:HGNC Symbol;Acc:HGNC:29597]","synonyms":"IFI1,LRG47,LRG-47,IRGM1","biotype":"protein_coding","ncbi_id":"345611","summary":"This gene encodes a member of the p47 immunity-related GTPase family. The encoded protein may play a role in the innate immune response by regulating autophagy formation in response to intracellular pathogens. Polymorphisms that affect the normal expression of this gene are associated with a susceptibility to Crohn's disease and tuberculosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2016]","start":150846523,"end":150900736,"strand":1,"description":"immunity related GTPase M [Source:HGNC Symbol;Acc:HGNC:29597]"}, {"versioned_ensembl_gene_id":"ENSG00000229960.1","gene_symbol":"AL590483.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":244068820,"end":244093026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254677.1","gene_symbol":"OSBPL9P2","gene_name":"oxysterol binding protein like 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130038","summary":null,"start":91114724,"end":91115951,"strand":-1,"description":"oxysterol binding protein like 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48732]"}, {"versioned_ensembl_gene_id":"ENSG00000279015.1","gene_symbol":"AC016717.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":225761559,"end":225762112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099821.13","gene_symbol":"POLRMT","gene_name":"RNA polymerase mitochondrial [Source:HGNC Symbol;Acc:HGNC:9200]","synonyms":"MTRPOL,MTRNAP,h-mtRPOL,APOLMT","biotype":"protein_coding","ncbi_id":"5442","summary":"This gene encodes a mitochondrial DNA-directed RNA polymerase. The gene product is responsible for mitochondrial gene expression as well as for providing RNA primers for initiation of replication of the mitochondrial genome. Although this polypeptide has the same function as the three nuclear DNA-directed RNA polymerases, it is more closely related to RNA polymerases of phage and mitochondrial polymerases of lower eukaryotes. [provided by RefSeq, Jul 2008]","start":617224,"end":633604,"strand":-1,"description":"RNA polymerase mitochondrial [Source:HGNC Symbol;Acc:HGNC:9200]"}, {"versioned_ensembl_gene_id":"ENSG00000118496.4","gene_symbol":"FBXO30","gene_name":"F-box protein 30 [Source:HGNC Symbol;Acc:HGNC:15600]","synonyms":"Fbx30,MGC21674","biotype":"protein_coding","ncbi_id":"84085","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it is upregulated in nasopharyngeal carcinoma. [provided by RefSeq, Jul 2008]","start":145793502,"end":145814753,"strand":-1,"description":"F-box protein 30 [Source:HGNC Symbol;Acc:HGNC:15600]"}, {"versioned_ensembl_gene_id":"ENSG00000185651.14","gene_symbol":"UBE2L3","gene_name":"ubiquitin conjugating enzyme E2 L3 [Source:HGNC Symbol;Acc:HGNC:12488]","synonyms":"UBCH7","biotype":"protein_coding","ncbi_id":"7332","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s) and ubiquitin-protein ligases (E3s). This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is demonstrated to participate in the ubiquitination of p53, c-Fos, and the NF-kB precursor p105 in vitro. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":21549447,"end":21624034,"strand":1,"description":"ubiquitin conjugating enzyme E2 L3 [Source:HGNC Symbol;Acc:HGNC:12488]"}, {"versioned_ensembl_gene_id":"ENSG00000183246.6","gene_symbol":"RIMBP3C","gene_name":"RIMS binding protein 3C [Source:HGNC Symbol;Acc:HGNC:33892]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150221","summary":null,"start":21545357,"end":21551461,"strand":-1,"description":"RIMS binding protein 3C [Source:HGNC Symbol;Acc:HGNC:33892]"}, {"versioned_ensembl_gene_id":"ENSG00000260000.2","gene_symbol":"AL133338.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100881471,"end":100882987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279798.1","gene_symbol":"AC018659.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97563257,"end":97563971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276039.1","gene_symbol":"AL353770.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66962271,"end":66962348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088367.21","gene_symbol":"EPB41L1","gene_name":"erythrocyte membrane protein band 4.1 like 1 [Source:HGNC Symbol;Acc:HGNC:3378]","synonyms":"KIAA0338,4.1N","biotype":"protein_coding","ncbi_id":"2036","summary":"Erythrocyte membrane protein band 4.1 (EPB41) is a multifunctional protein that mediates interactions between the erythrocyte cytoskeleton and the overlying plasma membrane. The encoded protein binds and stabilizes D2 and D3 dopamine receptors at the neuronal plasma membrane. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":36091504,"end":36232799,"strand":1,"description":"erythrocyte membrane protein band 4.1 like 1 [Source:HGNC Symbol;Acc:HGNC:3378]"}, {"versioned_ensembl_gene_id":"ENSG00000263588.1","gene_symbol":"AC091043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22088060,"end":22098780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255360.1","gene_symbol":"AP004607.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89955146,"end":89957165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090581.9","gene_symbol":"GNPTG","gene_name":"N-acetylglucosamine-1-phosphate transferase gamma subunit [Source:HGNC Symbol;Acc:HGNC:23026]","synonyms":"GNPTAG,CAB56184,c316G12.3,C16orf27","biotype":"protein_coding","ncbi_id":"84572","summary":"This gene encodes the gamma sunbunit of the N-acetylglucosamine-1-phosphotransferase complex. This hexameric complex, composed of alpha, beta and gamma subunits, catalyzes the first step in synthesis of a mannose 6-phosphate lysosomal recognition marker. This enzyme complex is necessary for targeting of lysosomal hydrolases to the lysosome. Mutations in the gene encoding the gamma subunit have been associated with mucolipidosis IIIC, also known as mucolipidosis III gamma.[provided by RefSeq, Feb 2010]","start":1351923,"end":1364113,"strand":1,"description":"N-acetylglucosamine-1-phosphate transferase gamma subunit [Source:HGNC Symbol;Acc:HGNC:23026]"}, {"versioned_ensembl_gene_id":"ENSG00000206480.11","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30717229,"end":30732250,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000267992.1","gene_symbol":"AC010605.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39030436,"end":39031323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070669.16","gene_symbol":"ASNS","gene_name":"asparagine synthetase (glutamine-hydrolyzing) [Source:HGNC Symbol;Acc:HGNC:753]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440","summary":"The protein encoded by this gene is involved in the synthesis of asparagine. This gene complements a mutation in the temperature-sensitive hamster mutant ts11, which blocks progression through the G1 phase of the cell cycle at nonpermissive temperature. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]","start":97852118,"end":97872542,"strand":-1,"description":"asparagine synthetase (glutamine-hydrolyzing) [Source:HGNC Symbol;Acc:HGNC:753]"}, {"versioned_ensembl_gene_id":"ENSG00000236822.1","gene_symbol":"AL589674.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142088233,"end":142089219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271402.1","gene_symbol":"IGKV2OR2-2","gene_name":"immunoglobulin kappa variable 2/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5808]","synonyms":"IGKV2/OR2-2","biotype":"IG_V_pseudogene","ncbi_id":"28859","summary":null,"start":97050729,"end":97051028,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5808]"}, {"versioned_ensembl_gene_id":"ENSG00000184677.16","gene_symbol":"ZBTB40","gene_name":"zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:HGNC:29045]","synonyms":"ZNF923,KIAA0478","biotype":"protein_coding","ncbi_id":"9923","summary":null,"start":22451851,"end":22531157,"strand":1,"description":"zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:HGNC:29045]"}, {"versioned_ensembl_gene_id":"ENSG00000236394.2","gene_symbol":"AL807752.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137052662,"end":137053375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278634.4","gene_symbol":"LILRA2","gene_name":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]","synonyms":"LIR7,LIR-7,ILT1,CD85h","biotype":"protein_coding","ncbi_id":"11027","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]","start":54503437,"end":54518077,"strand":1,"description":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]"}, {"versioned_ensembl_gene_id":"ENSG00000242019.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736536,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000220695.1","gene_symbol":"Z86062.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100530276,"end":100531052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258983.2","gene_symbol":"AL162171.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88499334,"end":88515502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239429.1","gene_symbol":"AF274854.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151611664,"end":151671196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235035.1","gene_symbol":"AC005234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70687142,"end":70691824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281335.1","gene_symbol":"MIF-AS1","gene_name":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]","synonyms":"LOC284889,MIF-AS","biotype":"antisense_RNA","ncbi_id":"284889","summary":null,"start":23894426,"end":23898930,"strand":-1,"description":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]"}, {"versioned_ensembl_gene_id":"ENSG00000223548.1","gene_symbol":"AC034228.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132003592,"end":132007022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099822.2","gene_symbol":"HCN2","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 [Source:HGNC Symbol;Acc:HGNC:4846]","synonyms":"HAC-1,BCNG2,BCNG-2","biotype":"protein_coding","ncbi_id":"610","summary":"The protein encoded by this gene is a hyperpolarization-activated cation channel involved in the generation of native pacemaker activity in the heart and in the brain. The encoded protein is activated by cAMP and can produce a fast, large current. Defects in this gene were noted as a possible cause of some forms of epilepsy. [provided by RefSeq, Jan 2017]","start":589893,"end":617159,"strand":1,"description":"hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 [Source:HGNC Symbol;Acc:HGNC:4846]"}, {"versioned_ensembl_gene_id":"ENSG00000281287.1","gene_symbol":"AP000350.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23862188,"end":23895223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111199.10","gene_symbol":"TRPV4","gene_name":"transient receptor potential cation channel subfamily V member 4 [Source:HGNC Symbol;Acc:HGNC:18083]","synonyms":"TRP12,OTRPC4,CMT2C,VROAC,VRL-2,VR-OAC","biotype":"protein_coding","ncbi_id":"59341","summary":"This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]","start":109783085,"end":109833401,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 4 [Source:HGNC Symbol;Acc:HGNC:18083]"}, {"versioned_ensembl_gene_id":"ENSG00000196653.11","gene_symbol":"ZNF502","gene_name":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]","synonyms":"FLJ14855,FLJ12515","biotype":"protein_coding","ncbi_id":"91392","summary":null,"start":44712643,"end":44723831,"strand":1,"description":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]"}, {"versioned_ensembl_gene_id":"ENSG00000260790.1","gene_symbol":"AC092338.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22374859,"end":22378180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228790.1","gene_symbol":"AC245128.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105550.8","gene_symbol":"FGF21","gene_name":"fibroblast growth factor 21 [Source:HGNC Symbol;Acc:HGNC:3678]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26291","summary":"Theis gene encodes a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. This protein is a secreted endocrine factor that functions as a major metabolic regulator. The encoded protein stimulates the uptake of glucose in adipose tissue. [provided by RefSeq, Mar 2016]","start":48755559,"end":48758330,"strand":1,"description":"fibroblast growth factor 21 [Source:HGNC Symbol;Acc:HGNC:3678]"}, {"versioned_ensembl_gene_id":"ENSG00000211878.1","gene_symbol":"TRAJ11","gene_name":"T-cell receptor alpha joining 11 [Source:HGNC Symbol;Acc:HGNC:12039]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28744","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22532502,"end":22532561,"strand":1,"description":"T-cell receptor alpha joining 11 [Source:HGNC Symbol;Acc:HGNC:12039]"}, {"versioned_ensembl_gene_id":"ENSG00000282952.1","gene_symbol":"AL583852.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78538391,"end":78551719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174951.10","gene_symbol":"FUT1","gene_name":"fucosyltransferase 1 (H blood group) [Source:HGNC Symbol;Acc:HGNC:4012]","synonyms":"HSC,H","biotype":"protein_coding","ncbi_id":"2523","summary":"This gene encodes a Golgi stack membrane protein that is involved in the creation of a precursor of the H antigen, which is required for the final step in the synthesis of soluble A and B antigens. This is one of two genes encoding the galactoside 2-L-fucosyltransferase enzyme. Mutations in this gene are a cause of the H-Bombay blood group. [provided by RefSeq, Aug 2016]","start":48748011,"end":48755390,"strand":-1,"description":"fucosyltransferase 1 (H blood group) [Source:HGNC Symbol;Acc:HGNC:4012]"}, {"versioned_ensembl_gene_id":"ENSG00000070778.12","gene_symbol":"PTPN21","gene_name":"protein tyrosine phosphatase, non-receptor type 21 [Source:HGNC Symbol;Acc:HGNC:9651]","synonyms":"PTPRL10,PTPD1","biotype":"protein_coding","ncbi_id":"11099","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal domain, similar to cytoskeletal- associated proteins including band 4.1, ezrin, merlin, and radixin. This PTP was shown to specially interact with BMX/ETK, a member of Tec tyrosine kinase family characterized by a multimodular structures including PH, SH3, and SH2 domains. The interaction of this PTP with BMX kinase was found to increase the activation of STAT3, but not STAT2 kinase. Studies of the similar gene in mice suggested the possible roles of this PTP in liver regeneration and spermatogenesis. [provided by RefSeq, Jul 2008]","start":88465778,"end":88554733,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 21 [Source:HGNC Symbol;Acc:HGNC:9651]"}, {"versioned_ensembl_gene_id":"ENSG00000230229.1","gene_symbol":"AC010163.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78352597,"end":78356100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282863.1","gene_symbol":"AC012560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78179174,"end":78675109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081019.13","gene_symbol":"RSBN1","gene_name":"round spermatid basic protein 1 [Source:HGNC Symbol;Acc:HGNC:25642]","synonyms":"ROSBIN,FLJ11220","biotype":"protein_coding","ncbi_id":"54665","summary":null,"start":113761832,"end":113812476,"strand":-1,"description":"round spermatid basic protein 1 [Source:HGNC Symbol;Acc:HGNC:25642]"}, {"versioned_ensembl_gene_id":"ENSG00000137700.17","gene_symbol":"SLC37A4","gene_name":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]","synonyms":"G6PT1,GSD1d,GSD1c,GSD1b,G6PT3,G6PT2","biotype":"protein_coding","ncbi_id":"2542","summary":"This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009]","start":119024114,"end":119030906,"strand":-1,"description":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]"}, {"versioned_ensembl_gene_id":"ENSG00000278220.2","gene_symbol":"CLN8","gene_name":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]","synonyms":"FLJ39417,EPMR,C8orf61","biotype":"protein_coding","ncbi_id":"2055","summary":"This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2017]","start":1755340,"end":1786132,"strand":1,"description":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]"}, {"versioned_ensembl_gene_id":"ENSG00000148346.11","gene_symbol":"LCN2","gene_name":"lipocalin 2 [Source:HGNC Symbol;Acc:HGNC:6526]","synonyms":"NGAL,24p3","biotype":"protein_coding","ncbi_id":"3934","summary":"This gene encodes a protein that belongs to the lipocalin family. Members of this family transport small hydrophobic molecules such as lipids, steroid hormones and retinoids. The protein encoded by this gene is a neutrophil gelatinase-associated lipocalin and plays a role in innate immunity by limiting bacterial growth as a result of sequestering iron-containing siderophores. The presence of this protein in blood and urine is an early biomarker of acute kidney injury. This protein is thought to be be involved in multiple cellular processes, including maintenance of skin homeostasis, and suppression of invasiveness and metastasis. Mice lacking this gene are more susceptible to bacterial infection than wild type mice. [provided by RefSeq, Sep 2015]","start":128149071,"end":128153455,"strand":1,"description":"lipocalin 2 [Source:HGNC Symbol;Acc:HGNC:6526]"}, {"versioned_ensembl_gene_id":"ENSG00000243478.9","gene_symbol":"AOX2P","gene_name":"aldehyde oxidase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:18450]","synonyms":"AOX2,AOH2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"344454","summary":null,"start":200738608,"end":200794239,"strand":1,"description":"aldehyde oxidase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:18450]"}, {"versioned_ensembl_gene_id":"ENSG00000138326.18","gene_symbol":"RPS24","gene_name":"ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:10411]","synonyms":"S24","biotype":"protein_coding","ncbi_id":"6229","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S24E family of ribosomal proteins. It is located in the cytoplasm. Multiple transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Mutations in this gene result in Diamond-Blackfan anemia. [provided by RefSeq, Nov 2008]","start":78033760,"end":78056812,"strand":1,"description":"ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:10411]"}, {"versioned_ensembl_gene_id":"ENSG00000265217.1","gene_symbol":"AC090358.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65606090,"end":65652053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272343.1","gene_symbol":"AC107952.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56222688,"end":56223173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264232.1","gene_symbol":"LINC01916","gene_name":"long intergenic non-protein coding RNA 1916 [Source:HGNC Symbol;Acc:HGNC:52735]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985128","summary":null,"start":65424013,"end":65447512,"strand":1,"description":"long intergenic non-protein coding RNA 1916 [Source:HGNC Symbol;Acc:HGNC:52735]"}, {"versioned_ensembl_gene_id":"ENSG00000235990.2","gene_symbol":"RPL23AP20","gene_name":"ribosomal protein L23a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645962","summary":null,"start":241916123,"end":241916543,"strand":1,"description":"ribosomal protein L23a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36622]"}, {"versioned_ensembl_gene_id":"ENSG00000280201.1","gene_symbol":"AP003400.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89576913,"end":89577652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074603.18","gene_symbol":"DPP8","gene_name":"dipeptidyl peptidase 8 [Source:HGNC Symbol;Acc:HGNC:16490]","synonyms":"DP8,MSTP141,MGC26191,FLJ20283,FLJ14920,DPRP1","biotype":"protein_coding","ncbi_id":"54878","summary":"This gene encodes a member of the peptidase S9B family, a small family of dipeptidyl peptidases that are able to cleave peptide substrates at a prolyl bond. The encoded protein shares similarity with dipeptidyl peptidase IV in that it is ubiquitously expressed, and hydrolyzes the same substrates. These similarities suggest that, like dipeptidyl peptidase IV, this protein may play a role in T-cell activation and immune function. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":65442463,"end":65517704,"strand":-1,"description":"dipeptidyl peptidase 8 [Source:HGNC Symbol;Acc:HGNC:16490]"}, {"versioned_ensembl_gene_id":"ENSG00000185963.13","gene_symbol":"BICD2","gene_name":"BICD cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17208]","synonyms":"KIAA0699","biotype":"protein_coding","ncbi_id":"23299","summary":"This gene is one of two human homologs of Drosophila bicaudal-D and a member of the Bicoid family. It has been implicated in dynein-mediated, minus end-directed motility along microtubules. It has also been reported to be a phosphorylation target of NIMA related kinase 8. Two alternative splice variants have been described. [provided by RefSeq, Jul 2008]","start":92711363,"end":92764812,"strand":-1,"description":"BICD cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17208]"}, {"versioned_ensembl_gene_id":"ENSG00000273622.1","gene_symbol":"CDC42EP5","gene_name":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]","synonyms":"CEP5,Borg3","biotype":"protein_coding","ncbi_id":"148170","summary":"Cell division control protein 42 (CDC42), a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to CDC42 and regulate its function negatively. The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding. The protein may also play a role in septin organization and inducing pseudopodia formation in fibroblasts [provided by RefSeq, Jul 2013]","start":54395351,"end":54403578,"strand":-1,"description":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]"}, {"versioned_ensembl_gene_id":"ENSG00000232197.1","gene_symbol":"AL596442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170162517,"end":170163027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164430.15","gene_symbol":"MB21D1","gene_name":"Mab-21 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21367]","synonyms":"cGAS,C6orf150","biotype":"protein_coding","ncbi_id":"115004","summary":null,"start":73413515,"end":73452276,"strand":-1,"description":"Mab-21 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21367]"}, {"versioned_ensembl_gene_id":"ENSG00000212916.4","gene_symbol":"MAP10","gene_name":"microtubule associated protein 10 [Source:HGNC Symbol;Acc:HGNC:29265]","synonyms":"MTR120,KIAA1383","biotype":"protein_coding","ncbi_id":"54627","summary":null,"start":232804892,"end":232808407,"strand":1,"description":"microtubule associated protein 10 [Source:HGNC Symbol;Acc:HGNC:29265]"}, {"versioned_ensembl_gene_id":"ENSG00000073584.18","gene_symbol":"SMARCE1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [Source:HGNC Symbol;Acc:HGNC:11109]","synonyms":"BAF57","biotype":"protein_coding","ncbi_id":"6605","summary":"The protein encoded by this gene is part of the large ATP-dependent chromatin remodeling complex SWI/SNF, which is required for transcriptional activation of genes normally repressed by chromatin. The encoded protein, either alone or when in the SWI/SNF complex, can bind to 4-way junction DNA, which is thought to mimic the topology of DNA as it enters or exits the nucleosome. The protein contains a DNA-binding HMG domain, but disruption of this domain does not abolish the DNA-binding or nucleosome-displacement activities of the SWI/SNF complex. Unlike most of the SWI/SNF complex proteins, this protein has no yeast counterpart. [provided by RefSeq, Jul 2008]","start":40624962,"end":40648508,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [Source:HGNC Symbol;Acc:HGNC:11109]"}, {"versioned_ensembl_gene_id":"ENSG00000264058.1","gene_symbol":"AC073508.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":40628797,"end":40665141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225427.1","gene_symbol":"LINC00331","gene_name":"long intergenic non-protein coding RNA 331 [Source:HGNC Symbol;Acc:HGNC:42048]","synonyms":"NCRNA00331","biotype":"lincRNA","ncbi_id":"100874126","summary":null,"start":78787319,"end":78792307,"strand":-1,"description":"long intergenic non-protein coding RNA 331 [Source:HGNC Symbol;Acc:HGNC:42048]"}, {"versioned_ensembl_gene_id":"ENSG00000228616.1","gene_symbol":"AF274858.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153610694,"end":153612925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232850.3","gene_symbol":"PTGES2-AS1","gene_name":"PTGES2 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:389791]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389791","summary":null,"start":128128529,"end":128130628,"strand":1,"description":"PTGES2 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:389791]"}, {"versioned_ensembl_gene_id":"ENSG00000221910.2","gene_symbol":"OR2F2","gene_name":"olfactory receptor family 2 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:8247]","synonyms":"OR7-1","biotype":"protein_coding","ncbi_id":"135948","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143935166,"end":143936279,"strand":1,"description":"olfactory receptor family 2 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:8247]"}, {"versioned_ensembl_gene_id":"ENSG00000258930.1","gene_symbol":"AC005230.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":71031686,"end":71031970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132275.10","gene_symbol":"RRP8","gene_name":"ribosomal RNA processing 8 [Source:HGNC Symbol;Acc:HGNC:29030]","synonyms":"NML,KIAA0409","biotype":"protein_coding","ncbi_id":"23378","summary":null,"start":6595075,"end":6603620,"strand":-1,"description":"ribosomal RNA processing 8 [Source:HGNC Symbol;Acc:HGNC:29030]"}, {"versioned_ensembl_gene_id":"ENSG00000128581.15","gene_symbol":"IFT22","gene_name":"intraflagellar transport 22 [Source:HGNC Symbol;Acc:HGNC:21895]","synonyms":"RABL5,FLJ14117,FLJ13225,DKFZp761N0823","biotype":"protein_coding","ncbi_id":"64792","summary":null,"start":101313367,"end":101321823,"strand":-1,"description":"intraflagellar transport 22 [Source:HGNC Symbol;Acc:HGNC:21895]"}, {"versioned_ensembl_gene_id":"ENSG00000185433.8","gene_symbol":"LINC00158","gene_name":"long intergenic non-protein coding RNA 158 [Source:HGNC Symbol;Acc:HGNC:1283]","synonyms":"NCRNA00158,C21orf42","biotype":"lincRNA","ncbi_id":"54072","summary":null,"start":25385820,"end":25431701,"strand":-1,"description":"long intergenic non-protein coding RNA 158 [Source:HGNC Symbol;Acc:HGNC:1283]"}, {"versioned_ensembl_gene_id":"ENSG00000054983.16","gene_symbol":"GALC","gene_name":"galactosylceramidase [Source:HGNC Symbol;Acc:HGNC:4115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2581","summary":"This gene encodes a lysosomal protein which hydrolyzes the galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. Mutations in this gene have been associated with Krabbe disease, also known as globoid cell leukodystrophy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":87837820,"end":87993665,"strand":-1,"description":"galactosylceramidase [Source:HGNC Symbol;Acc:HGNC:4115]"}, {"versioned_ensembl_gene_id":"ENSG00000167106.11","gene_symbol":"FAM102A","gene_name":"family with sequence similarity 102 member A [Source:HGNC Symbol;Acc:HGNC:31419]","synonyms":"SYM-3A,Eeig1,C9orf132,bA203J24.7","biotype":"protein_coding","ncbi_id":"399665","summary":null,"start":127940579,"end":127980513,"strand":-1,"description":"family with sequence similarity 102 member A [Source:HGNC Symbol;Acc:HGNC:31419]"}, {"versioned_ensembl_gene_id":"ENSG00000238114.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31571300,"end":31573267,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000258505.1","gene_symbol":"AL442163.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":42608868,"end":42609577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255075.1","gene_symbol":"CENPUP1","gene_name":"centromere protein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130384","summary":null,"start":13756027,"end":13757560,"strand":1,"description":"centromere protein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49889]"}, {"versioned_ensembl_gene_id":"ENSG00000148296.6","gene_symbol":"SURF6","gene_name":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]","synonyms":"RRP14,FLJ30322","biotype":"protein_coding","ncbi_id":"6838","summary":"This gene encodes a conserved protein that is localized to the nucleolus. The encoded protein may function as a nucleolar-matrix protein with nucleic acid-binding properties. There is a pseudogene for this gene on chromosome Y. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133328774,"end":133336398,"strand":-1,"description":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]"}, {"versioned_ensembl_gene_id":"ENSG00000226717.2","gene_symbol":"PTPRD-AS2","gene_name":"PTPRD antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:49754]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929428","summary":null,"start":10613202,"end":10620420,"strand":1,"description":"PTPRD antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:49754]"}, {"versioned_ensembl_gene_id":"ENSG00000231701.1","gene_symbol":"BMS1P13","gene_name":"BMS1, ribosome biogenesis factor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49158]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644716","summary":null,"start":65828120,"end":65831696,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49158]"}, {"versioned_ensembl_gene_id":"ENSG00000249987.1","gene_symbol":"RPS4XP20","gene_name":"ribosomal protein S4X pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36437]","synonyms":"RPS4P20","biotype":"processed_pseudogene","ncbi_id":"100271386","summary":null,"start":34022656,"end":34023427,"strand":-1,"description":"ribosomal protein S4X pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36437]"}, {"versioned_ensembl_gene_id":"ENSG00000133275.15","gene_symbol":"CSNK1G2","gene_name":"casein kinase 1 gamma 2 [Source:HGNC Symbol;Acc:HGNC:2455]","synonyms":"CK1g2","biotype":"protein_coding","ncbi_id":"1455","summary":null,"start":1941149,"end":1981338,"strand":1,"description":"casein kinase 1 gamma 2 [Source:HGNC Symbol;Acc:HGNC:2455]"}, {"versioned_ensembl_gene_id":"ENSG00000176318.8","gene_symbol":"FOXN3P1","gene_name":"forkhead box N3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43882]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643976","summary":null,"start":102546734,"end":102548213,"strand":-1,"description":"forkhead box N3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43882]"}, {"versioned_ensembl_gene_id":"ENSG00000218510.7","gene_symbol":"LINC00339","gene_name":"long intergenic non-protein coding RNA 339 [Source:HGNC Symbol;Acc:HGNC:25011]","synonyms":"NCRNA00339,HSPC157","biotype":"transcribed_processed_pseudogene","ncbi_id":"29092","summary":null,"start":22024558,"end":22031223,"strand":1,"description":"long intergenic non-protein coding RNA 339 [Source:HGNC Symbol;Acc:HGNC:25011]"}, {"versioned_ensembl_gene_id":"ENSG00000107807.12","gene_symbol":"TLX1","gene_name":"T-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5056]","synonyms":"TCL3,HOX11","biotype":"protein_coding","ncbi_id":"3195","summary":"This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes. The encoded protein is required for normal development of the spleen during embryogenesis. This protein is also involved in specification of neuronal cell fates. Ectopic expression of this gene due to chromosomal translocations is associated with certain T-cell acute lymphoblastic leukemias. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":101130505,"end":101137789,"strand":1,"description":"T-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5056]"}, {"versioned_ensembl_gene_id":"ENSG00000228169.3","gene_symbol":"PPIAP19","gene_name":"peptidylprolyl isomerase A pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:31663]","synonyms":"bA108K1.2","biotype":"processed_pseudogene","ncbi_id":"390006","summary":null,"start":114690143,"end":114690634,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:31663]"}, {"versioned_ensembl_gene_id":"ENSG00000240388.2","gene_symbol":"AC008799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91354478,"end":91354934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277447.1","gene_symbol":"AP005431.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3025069,"end":3025387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204414.12","gene_symbol":"CSHL1","gene_name":"chorionic somatomammotropin hormone like 1 [Source:HGNC Symbol;Acc:HGNC:2442]","synonyms":"MGC149868,hCS-L,CSL,CSHP1,CS-5","biotype":"protein_coding","ncbi_id":"1444","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. This particular family member is expressed in placental villi, although it was originally thought to be a pseudogene. In fact, alternative splicing suggests that the majority of the transcripts would be unable to express a secreted protein. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":63909597,"end":63918838,"strand":-1,"description":"chorionic somatomammotropin hormone like 1 [Source:HGNC Symbol;Acc:HGNC:2442]"}, {"versioned_ensembl_gene_id":"ENSG00000108352.11","gene_symbol":"RAPGEFL1","gene_name":"Rap guanine nucleotide exchange factor like 1 [Source:HGNC Symbol;Acc:HGNC:17428]","synonyms":"Link-GEFII","biotype":"protein_coding","ncbi_id":"51195","summary":null,"start":40177010,"end":40195656,"strand":1,"description":"Rap guanine nucleotide exchange factor like 1 [Source:HGNC Symbol;Acc:HGNC:17428]"}, {"versioned_ensembl_gene_id":"ENSG00000282240.1","gene_symbol":"TRBV6-4","gene_name":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]","synonyms":"TRBV64,TCRBV6S4,TCRBV13S5","biotype":"TR_V_gene","ncbi_id":"28603","summary":null,"start":142402503,"end":142402958,"strand":1,"description":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]"}, {"versioned_ensembl_gene_id":"ENSG00000134202.10","gene_symbol":"GSTM3","gene_name":"glutathione S-transferase mu 3 [Source:HGNC Symbol;Acc:HGNC:4635]","synonyms":"GST5","biotype":"protein_coding","ncbi_id":"2947","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":109733932,"end":109741038,"strand":-1,"description":"glutathione S-transferase mu 3 [Source:HGNC Symbol;Acc:HGNC:4635]"}, {"versioned_ensembl_gene_id":"ENSG00000241720.2","gene_symbol":"AL158847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109725820,"end":109775252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251093.1","gene_symbol":"AC093281.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91226475,"end":91227071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276327.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54905478,"end":54919948,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000275937.1","gene_symbol":"GU182339.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54770973,"end":54780252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137168.7","gene_symbol":"PPIL1","gene_name":"peptidylprolyl isomerase like 1 [Source:HGNC Symbol;Acc:HGNC:9260]","synonyms":"CYPL1","biotype":"protein_coding","ncbi_id":"51645","summary":"This gene is a member of the cyclophilin family of peptidylprolyl isomerases (PPIases). The cyclophilins are a highly conserved, ubiquitous family, members of which play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. Based on similarity to other PPIases, this protein could accelerate the folding of proteins and might catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. [provided by RefSeq, Jul 2008]","start":36854827,"end":36875024,"strand":-1,"description":"peptidylprolyl isomerase like 1 [Source:HGNC Symbol;Acc:HGNC:9260]"}, {"versioned_ensembl_gene_id":"ENSG00000278306.1","gene_symbol":"KIR2DS3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]","synonyms":"nkat7","biotype":"protein_coding","ncbi_id":"3808","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54782354,"end":54796789,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]"}, {"versioned_ensembl_gene_id":"ENSG00000206287.5","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33137310,"end":33141537,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000232379.1","gene_symbol":"AL390879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136947748,"end":136948133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143164.15","gene_symbol":"DCAF6","gene_name":"DDB1 and CUL4 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:30002]","synonyms":"PC326,IQWD1","biotype":"protein_coding","ncbi_id":"55827","summary":"The protein encoded by this gene is a ligand-dependent coactivator of nuclear receptors, including nuclear receptor subfamily 3 group C member 1 (NR3C1), glucocorticoid receptor (GR), and androgen receptor (AR). The encoded protein and DNA damage binding protein 2 (DDB2) may act as tumor promoters and tumor suppressors, respectively, by regulating the level of androgen receptor in prostate tissues. In addition, this protein can act with glucocorticoid receptor to promote human papillomavirus gene expression. [provided by RefSeq, Mar 2017]","start":167935783,"end":168075843,"strand":1,"description":"DDB1 and CUL4 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:30002]"}, {"versioned_ensembl_gene_id":"ENSG00000253629.1","gene_symbol":"AP000426.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101686547,"end":101689093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251199.5","gene_symbol":"AC109830.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134255173,"end":134327473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211820.1","gene_symbol":"TRAV41","gene_name":"T-cell receptor alpha variable 41 [Source:HGNC Symbol;Acc:HGNC:12142]","synonyms":"TCRAV41S1,TCRAV19S1","biotype":"TR_V_gene","ncbi_id":"28640","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22320188,"end":22320691,"strand":1,"description":"T-cell receptor alpha variable 41 [Source:HGNC Symbol;Acc:HGNC:12142]"}, {"versioned_ensembl_gene_id":"ENSG00000189238.5","gene_symbol":"LINC00943","gene_name":"long intergenic non-protein coding RNA 943 [Source:HGNC Symbol;Acc:HGNC:48639]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507206","summary":null,"start":126726270,"end":126746252,"strand":1,"description":"long intergenic non-protein coding RNA 943 [Source:HGNC Symbol;Acc:HGNC:48639]"}, {"versioned_ensembl_gene_id":"ENSG00000280013.1","gene_symbol":"CU639417.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6008604,"end":6008810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237405.10","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32188640,"end":32191996,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000237283.1","gene_symbol":"AL691515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188705623,"end":188710880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150732.8","gene_symbol":"AL136372.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188067298,"end":188067525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279784.1","gene_symbol":"FP236315.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5705345,"end":5707160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211817.2","gene_symbol":"TRAV38-2DV8","gene_name":"T-cell receptor alpha variable 38-2/delta variable 8 [Source:HGNC Symbol;Acc:HGNC:12138]","synonyms":"TRAV382DV8,TRAV38-2/DV8,TCRAV14S1,hADV38S2","biotype":"TR_V_gene","ncbi_id":"28643","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22281105,"end":22281748,"strand":1,"description":"T-cell receptor alpha variable 38-2/delta variable 8 [Source:HGNC Symbol;Acc:HGNC:12138]"}, {"versioned_ensembl_gene_id":"ENSG00000238285.1","gene_symbol":"MRPL50P2","gene_name":"mitochondrial ribosomal protein L50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359749","summary":null,"start":203315390,"end":203315871,"strand":-1,"description":"mitochondrial ribosomal protein L50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29720]"}, {"versioned_ensembl_gene_id":"ENSG00000233620.5","gene_symbol":"AC093581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216072465,"end":216086917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139899.10","gene_symbol":"CBLN3","gene_name":"cerebellin 3 precursor [Source:HGNC Symbol;Acc:HGNC:20146]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643866","summary":"Members of the precerebellin family, such as CBLN3, contain a cerebellin motif (see CBLN1; MIM 600432) and a C-terminal C1q signature domain (see MIM 120550) that mediates trimeric assembly of atypical collagen complexes. However, precerebellins do not contain a collagen motif, suggesting that they are not conventional components of the extracellular matrix (Pang et al., 2000 [PubMed 10964938]).[supplied by OMIM, Aug 2009]","start":24426532,"end":24430954,"strand":-1,"description":"cerebellin 3 precursor [Source:HGNC Symbol;Acc:HGNC:20146]"}, {"versioned_ensembl_gene_id":"ENSG00000276450.1","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54905329,"end":54909244,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000229852.2","gene_symbol":"AC019205.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73263215,"end":73301401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116793.15","gene_symbol":"PHTF1","gene_name":"putative homeodomain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:8939]","synonyms":"PHTF","biotype":"protein_coding","ncbi_id":"10745","summary":null,"start":113696831,"end":113759489,"strand":-1,"description":"putative homeodomain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:8939]"}, {"versioned_ensembl_gene_id":"ENSG00000105501.12","gene_symbol":"SIGLEC5","gene_name":"sialic acid binding Ig like lectin 5 [Source:HGNC Symbol;Acc:HGNC:10874]","synonyms":"OB-BP2,CD33L2,CD170,SIGLEC-5","biotype":"protein_coding","ncbi_id":"8778","summary":"This gene encodes a member of the sialic acid-binding immunoglobulin-like lectin (Siglec) family. These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain. The encoded protein is a member of the CD33-related subset of Siglecs and inhibits the activation of several cell types including monocytes, macrophages and neutrophils. Binding of group B Streptococcus (GBS) to the encoded protein plays a role in GBS immune evasion. [provided by RefSeq, Feb 2012]","start":51611927,"end":51645545,"strand":-1,"description":"sialic acid binding Ig like lectin 5 [Source:HGNC Symbol;Acc:HGNC:10874]"}, {"versioned_ensembl_gene_id":"ENSG00000108602.17","gene_symbol":"ALDH3A1","gene_name":"aldehyde dehydrogenase 3 family member A1 [Source:HGNC Symbol;Acc:HGNC:405]","synonyms":"ALDH3","biotype":"protein_coding","ncbi_id":"218","summary":"Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain (6 carbons or more) saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2008]","start":19737984,"end":19748943,"strand":-1,"description":"aldehyde dehydrogenase 3 family member A1 [Source:HGNC Symbol;Acc:HGNC:405]"}, {"versioned_ensembl_gene_id":"ENSG00000276293.4","gene_symbol":"PIP4K2B","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]","synonyms":"PIP5KIIbeta,PIP5KIIB,PIP5K2B","biotype":"protein_coding","ncbi_id":"8396","summary":"The protein encoded by this gene catalyzes the phosphorylation of phosphatidylinositol-5-phosphate on the fourth hydroxyl of the myo-inositol ring to form phosphatidylinositol-5,4-bisphosphate. This gene is a member of the phosphatidylinositol-5-phosphate 4-kinase family. The encoded protein sequence does not show similarity to other kinases, but the protein does exhibit kinase activity. Additionally, the encoded protein interacts with p55 TNF receptor. [provided by RefSeq, Jul 2008]","start":38765689,"end":38800126,"strand":-1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]"}, {"versioned_ensembl_gene_id":"ENSG00000282477.1","gene_symbol":"AC100803.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141443230,"end":141443856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244071.1","gene_symbol":"RPL9P33","gene_name":"ribosomal protein L9 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271229","summary":null,"start":51621136,"end":51621701,"strand":1,"description":"ribosomal protein L9 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36273]"}, {"versioned_ensembl_gene_id":"ENSG00000232145.1","gene_symbol":"AC099548.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143796295,"end":143796720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241136.1","gene_symbol":"PAICSP6","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780812","summary":null,"start":143782667,"end":143784284,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38099]"}, {"versioned_ensembl_gene_id":"ENSG00000196735.11","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32628179,"end":32647062,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000251497.2","gene_symbol":"PITPNM2-AS1","gene_name":"PITPNM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53391]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507091","summary":null,"start":123081384,"end":123084744,"strand":1,"description":"PITPNM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53391]"}, {"versioned_ensembl_gene_id":"ENSG00000250057.1","gene_symbol":"AC114781.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83233512,"end":83247213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167716.18","gene_symbol":"WDR81","gene_name":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]","synonyms":"FLJ33817,CAMRQ2,SORF-2,PPP1R166","biotype":"protein_coding","ncbi_id":"124997","summary":"This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":1716523,"end":1738599,"strand":1,"description":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]"}, {"versioned_ensembl_gene_id":"ENSG00000279568.1","gene_symbol":"AC093525.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2575628,"end":2577373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153885.14","gene_symbol":"KCTD15","gene_name":"potassium channel tetramerization domain containing 15 [Source:HGNC Symbol;Acc:HGNC:23297]","synonyms":"MGC25497","biotype":"protein_coding","ncbi_id":"79047","summary":null,"start":33795933,"end":33815763,"strand":1,"description":"potassium channel tetramerization domain containing 15 [Source:HGNC Symbol;Acc:HGNC:23297]"}, {"versioned_ensembl_gene_id":"ENSG00000229524.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31626429,"end":31640114,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000277238.2","gene_symbol":"TAS2R10","gene_name":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]","synonyms":"TRB2,T2R10","biotype":"protein_coding","ncbi_id":"50839","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10825317,"end":10826358,"strand":-1,"description":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]"}, {"versioned_ensembl_gene_id":"ENSG00000270132.1","gene_symbol":"WISP1-OT1","gene_name":"WISP1 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49126]","synonyms":"WISP1-UT1","biotype":"sense_intronic","ncbi_id":"106144543","summary":null,"start":133229056,"end":133229697,"strand":1,"description":"WISP1 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49126]"}, {"versioned_ensembl_gene_id":"ENSG00000165775.17","gene_symbol":"FUNDC2","gene_name":"FUN14 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24925]","synonyms":"HCBP6,DC44","biotype":"protein_coding","ncbi_id":"65991","summary":null,"start":155025980,"end":155060303,"strand":1,"description":"FUN14 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24925]"}, {"versioned_ensembl_gene_id":"ENSG00000064225.12","gene_symbol":"ST3GAL6","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18080]","synonyms":"ST3GALVI,SIAT10","biotype":"protein_coding","ncbi_id":"10402","summary":"The protein encoded by this gene is a member of the sialyltransferase family. Members of this family are enzymes that transfer sialic acid from the activated cytidine 5'-monophospho-N-acetylneuraminic acid to terminal positions on sialylated glycolipids (gangliosides) or to the N- or O-linked sugar chains of glycoproteins. This protein has high specificity for neolactotetraosylceramide and neolactohexaosylceramide as glycolipid substrates and may contribute to the formation of selectin ligands and sialyl Lewis X, a carbohydrate important for cell-to-cell recognition and a blood group antigen. [provided by RefSeq, Apr 2016]","start":98732236,"end":98821201,"strand":1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18080]"}, {"versioned_ensembl_gene_id":"ENSG00000099804.8","gene_symbol":"CDC34","gene_name":"cell division cycle 34 [Source:HGNC Symbol;Acc:HGNC:1734]","synonyms":"UBE2R1,UBC3,E2-CDC34","biotype":"protein_coding","ncbi_id":"997","summary":"The protein encoded by this gene is a member of the ubiquitin-conjugating enzyme family. Ubiquitin-conjugating enzyme catalyzes the covalent attachment of ubiquitin to other proteins. This protein is a part of the large multiprotein complex, which is required for ubiquitin-mediated degradation of cell cycle G1 regulators, and for the initiation of DNA replication. [provided by RefSeq, Jul 2008]","start":531712,"end":542092,"strand":1,"description":"cell division cycle 34 [Source:HGNC Symbol;Acc:HGNC:1734]"}, {"versioned_ensembl_gene_id":"ENSG00000064270.12","gene_symbol":"ATP2C2","gene_name":"ATPase secretory pathway Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:29103]","synonyms":"SPCA2,KIAA0703","biotype":"protein_coding","ncbi_id":"9914","summary":null,"start":84368527,"end":84464187,"strand":1,"description":"ATPase secretory pathway Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:29103]"}, {"versioned_ensembl_gene_id":"ENSG00000067842.17","gene_symbol":"ATP2B3","gene_name":"ATPase plasma membrane Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:816]","synonyms":"SCAX1,PMCA3,CLA2,CFAP39","biotype":"protein_coding","ncbi_id":"492","summary":"The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 3. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":153517676,"end":153582939,"strand":1,"description":"ATPase plasma membrane Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:816]"}, {"versioned_ensembl_gene_id":"ENSG00000270276.2","gene_symbol":"HIST2H4B","gene_name":"histone cluster 2 H4 family member b [Source:HGNC Symbol;Acc:HGNC:29607]","synonyms":"H4/o","biotype":"protein_coding","ncbi_id":"554313","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-dependent histone that is a member of the histone H4 family. Some transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the telomeric copy. [provided by RefSeq, May 2020]","start":149854045,"end":149861210,"strand":-1,"description":"histone cluster 2 H4 family member b [Source:HGNC Symbol;Acc:HGNC:29607]"}, {"versioned_ensembl_gene_id":"ENSG00000268892.1","gene_symbol":"AC010620.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21221645,"end":21222746,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117016.9","gene_symbol":"RIMS3","gene_name":"regulating synaptic membrane exocytosis 3 [Source:HGNC Symbol;Acc:HGNC:21292]","synonyms":"RIM3,NIM3","biotype":"protein_coding","ncbi_id":"9783","summary":null,"start":40620679,"end":40665657,"strand":-1,"description":"regulating synaptic membrane exocytosis 3 [Source:HGNC Symbol;Acc:HGNC:21292]"}, {"versioned_ensembl_gene_id":"ENSG00000236786.1","gene_symbol":"TSPY15P","gene_name":"testis specific protein, Y-linked 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:37474]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642631","summary":null,"start":9548108,"end":9550681,"strand":1,"description":"testis specific protein, Y-linked 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:37474]"}, {"versioned_ensembl_gene_id":"ENSG00000146063.19","gene_symbol":"TRIM41","gene_name":"tripartite motif containing 41 [Source:HGNC Symbol;Acc:HGNC:19013]","synonyms":"RINCK,MGC1127","biotype":"protein_coding","ncbi_id":"90933","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM family is characterized by a signature motif composed of a RING finger, one or more B-box domains, and a coiled-coil region. This encoded protein may play a role in protein kinase C signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":181222499,"end":181235809,"strand":1,"description":"tripartite motif containing 41 [Source:HGNC Symbol;Acc:HGNC:19013]"}, {"versioned_ensembl_gene_id":"ENSG00000254579.1","gene_symbol":"AC013488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40445304,"end":40447141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278698.1","gene_symbol":"AL162574.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106773623,"end":106774279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137502.9","gene_symbol":"RAB30","gene_name":"RAB30, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9770]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27314","summary":null,"start":82973133,"end":83071923,"strand":-1,"description":"RAB30, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9770]"}, {"versioned_ensembl_gene_id":"ENSG00000266916.5","gene_symbol":"ZNF793-AS1","gene_name":"ZNF793 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51303]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927720","summary":null,"start":37497159,"end":37507046,"strand":-1,"description":"ZNF793 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51303]"}, {"versioned_ensembl_gene_id":"ENSG00000259067.1","gene_symbol":"AL583810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104904342,"end":104905204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261219.1","gene_symbol":"AC090651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57720295,"end":57720928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261270.1","gene_symbol":"AC012181.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56940278,"end":56941342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224216.1","gene_symbol":"AC234781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155334858,"end":155351957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261114.1","gene_symbol":"AC012181.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56941028,"end":56941726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225108.1","gene_symbol":"ZBTB45P1","gene_name":"zinc finger and BTB domain containing 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49227]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645129","summary":null,"start":109986939,"end":109988394,"strand":-1,"description":"zinc finger and BTB domain containing 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49227]"}, {"versioned_ensembl_gene_id":"ENSG00000104635.13","gene_symbol":"SLC39A14","gene_name":"solute carrier family 39 member 14 [Source:HGNC Symbol;Acc:HGNC:20858]","synonyms":"ZIP14,NET34,KIAA0062","biotype":"protein_coding","ncbi_id":"23516","summary":"This gene encodes a member of the the SLC39A family of divalent metal transporters that mediates the cellular uptake of manganese, zinc, iron, and cadmium. The encoded protein contains eight transmembrane domains, a histidine-rich motif, and a metalloprotease motif, and is expressed on the plasma membrane and the endocytic vesicle membrane. It is an important transporter of nontransferrin-bound iron and a critical regulator of manganese homeostasis. Naturally occurring mutations in this gene are associated with neurodegeneration with brain iron accumulation and early-onset parkinsonism-dystonia with hypermanganesemia. [provided by RefSeq, May 2017]","start":22367249,"end":22434129,"strand":1,"description":"solute carrier family 39 member 14 [Source:HGNC Symbol;Acc:HGNC:20858]"}, {"versioned_ensembl_gene_id":"ENSG00000196301.3","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32459821,"end":32473500,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000144792.9","gene_symbol":"ZNF660","gene_name":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]","synonyms":"FLJ36870","biotype":"protein_coding","ncbi_id":"285349","summary":"This gene encodes a protein that contains multiple C2H2 zinc finger domains, and is located in a cluster of zinc-finger encoding genes on chromosome 3. Naturally-occurring readthrough transcription is observed between this gene and the downstream zinc finger protein 197 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017]","start":44578223,"end":44599694,"strand":1,"description":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]"}, {"versioned_ensembl_gene_id":"ENSG00000265751.1","gene_symbol":"AC015878.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21380286,"end":21451017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251051.1","gene_symbol":"ELL2P2","gene_name":"elongation factor for RNA polymerase II 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421143","summary":null,"start":132367786,"end":132368479,"strand":-1,"description":"elongation factor for RNA polymerase II 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39344]"}, {"versioned_ensembl_gene_id":"ENSG00000109610.5","gene_symbol":"SOD3","gene_name":"superoxide dismutase 3 [Source:HGNC Symbol;Acc:HGNC:11181]","synonyms":"EC-SOD","biotype":"protein_coding","ncbi_id":"6649","summary":"This gene encodes a member of the superoxide dismutase (SOD) protein family. SODs are antioxidant enzymes that catalyze the conversion of superoxide radicals into hydrogen peroxide and oxygen, which may protect the brain, lungs, and other tissues from oxidative stress. Proteolytic processing of the encoded protein results in the formation of two distinct homotetramers that differ in their ability to interact with the extracellular matrix (ECM). Homotetramers consisting of the intact protein, or type C subunit, exhibit high affinity for heparin and are anchored to the ECM. Homotetramers consisting of a proteolytically cleaved form of the protein, or type A subunit, exhibit low affinity for heparin and do not interact with the ECM. A mutation in this gene may be associated with increased heart disease risk. [provided by RefSeq, Oct 2015]","start":24789912,"end":24800842,"strand":1,"description":"superoxide dismutase 3 [Source:HGNC Symbol;Acc:HGNC:11181]"}, {"versioned_ensembl_gene_id":"ENSG00000254081.1","gene_symbol":"LINC01299","gene_name":"long intergenic non-protein coding RNA 1299 [Source:HGNC Symbol;Acc:HGNC:27839]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286186","summary":null,"start":65527008,"end":65562780,"strand":-1,"description":"long intergenic non-protein coding RNA 1299 [Source:HGNC Symbol;Acc:HGNC:27839]"}, {"versioned_ensembl_gene_id":"ENSG00000243007.1","gene_symbol":"RPL12P35","gene_name":"ribosomal protein L12 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400389","summary":null,"start":72379215,"end":72379710,"strand":-1,"description":"ribosomal protein L12 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35969]"}, {"versioned_ensembl_gene_id":"ENSG00000137819.13","gene_symbol":"PAQR5","gene_name":"progestin and adipoQ receptor family member 5 [Source:HGNC Symbol;Acc:HGNC:29645]","synonyms":"MPRG,FLJ20190","biotype":"protein_coding","ncbi_id":"54852","summary":null,"start":69298947,"end":69407780,"strand":1,"description":"progestin and adipoQ receptor family member 5 [Source:HGNC Symbol;Acc:HGNC:29645]"}, {"versioned_ensembl_gene_id":"ENSG00000279659.1","gene_symbol":"AL451064.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79573877,"end":79575530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253470.1","gene_symbol":"AC016074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125749055,"end":125750241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271356.1","gene_symbol":"AC073091.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76260755,"end":76261661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079950.13","gene_symbol":"STX7","gene_name":"syntaxin 7 [Source:HGNC Symbol;Acc:HGNC:11442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8417","summary":"The protein encoded by this gene is a syntaxin family membrane receptor involved in vesicle transport. The encoded protein binds alpha-SNAP, an important regulator of transport vesicle fusion. Along with syntaxin 13, this protein plays a role in the ordered fusion of endosomes and lysosomes with the phagosome. [provided by RefSeq, May 2016]","start":132445867,"end":132513198,"strand":-1,"description":"syntaxin 7 [Source:HGNC Symbol;Acc:HGNC:11442]"}, {"versioned_ensembl_gene_id":"ENSG00000143320.8","gene_symbol":"CRABP2","gene_name":"cellular retinoic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2339]","synonyms":"CRABP-II","biotype":"protein_coding","ncbi_id":"1382","summary":"This gene encodes a member of the retinoic acid (RA, a form of vitamin A) binding protein family and lipocalin/cytosolic fatty-acid binding protein family. The protein is a cytosol-to-nuclear shuttling protein, which facilitates RA binding to its cognate receptor complex and transfer to the nucleus. It is involved in the retinoid signaling pathway, and is associated with increased circulating low-density lipoprotein cholesterol. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2010]","start":156699606,"end":156705816,"strand":-1,"description":"cellular retinoic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2339]"}, {"versioned_ensembl_gene_id":"ENSG00000225107.1","gene_symbol":"AC092484.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145569294,"end":145588024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280094.2","gene_symbol":"OR1B1","gene_name":"olfactory receptor family 1 subfamily B member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8181]","synonyms":"OR9-B","biotype":"polymorphic_pseudogene","ncbi_id":"347169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":122628579,"end":122629573,"strand":-1,"description":"olfactory receptor family 1 subfamily B member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8181]"}, {"versioned_ensembl_gene_id":"ENSG00000140939.14","gene_symbol":"NOL3","gene_name":"nucleolar protein 3 [Source:HGNC Symbol;Acc:HGNC:7869]","synonyms":"NOP30,MYP,CARD2,ARC","biotype":"protein_coding","ncbi_id":"8996","summary":"This gene encodes an anti-apoptotic protein that has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":67170154,"end":67175735,"strand":1,"description":"nucleolar protein 3 [Source:HGNC Symbol;Acc:HGNC:7869]"}, {"versioned_ensembl_gene_id":"ENSG00000139537.10","gene_symbol":"CCDC65","gene_name":"coiled-coil domain containing 65 [Source:HGNC Symbol;Acc:HGNC:29937]","synonyms":"NYD-SP28,FLJ35732,FAP250,DRC2,CILD27,CFAP250","biotype":"protein_coding","ncbi_id":"85478","summary":"This gene encodes a sperm tail protein that is highly expressed in adult testis, spermatocytes and spermatids. The protein plays a critical role in the assembly of the nexin-dynein regulatory complex. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]","start":48904110,"end":48931840,"strand":1,"description":"coiled-coil domain containing 65 [Source:HGNC Symbol;Acc:HGNC:29937]"}, {"versioned_ensembl_gene_id":"ENSG00000226347.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"dJ80I19.4,OR6-8,hs6M1-6","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173273,"end":29174544,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000134287.9","gene_symbol":"ARF3","gene_name":"ADP ribosylation factor 3 [Source:HGNC Symbol;Acc:HGNC:654]","synonyms":null,"biotype":"protein_coding","ncbi_id":"377","summary":"ADP-ribosylation factor 3 (ARF3) is a member of the human ARF gene family. These genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The gene products include 6 ARF proteins and 11 ARF-like proteins and constitute 1 family of the RAS superfamily. The ARF proteins are categorized as class I (ARF1, ARF2,and ARF3), class II (ARF4 and ARF5) and class III (ARF6) and members of each class share a common gene organization. The ARF3 gene contains five exons and four introns. [provided by RefSeq, Jul 2008]","start":48935723,"end":48957551,"strand":-1,"description":"ADP ribosylation factor 3 [Source:HGNC Symbol;Acc:HGNC:654]"}, {"versioned_ensembl_gene_id":"ENSG00000284721.1","gene_symbol":"AL662907.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33194788,"end":33200353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233880.1","gene_symbol":"AL161722.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35761499,"end":35762479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215351.3","gene_symbol":"PPIAP1","gene_name":"peptidylprolyl isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9254]","synonyms":"PPIAP","biotype":"processed_pseudogene","ncbi_id":"100288185","summary":null,"start":20828127,"end":20828622,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9254]"}, {"versioned_ensembl_gene_id":"ENSG00000145975.14","gene_symbol":"FAM217A","gene_name":"family with sequence similarity 217 member A [Source:HGNC Symbol;Acc:HGNC:21362]","synonyms":"MGC43581,C6orf146","biotype":"protein_coding","ncbi_id":"222826","summary":null,"start":4049434,"end":4087344,"strand":-1,"description":"family with sequence similarity 217 member A [Source:HGNC Symbol;Acc:HGNC:21362]"}, {"versioned_ensembl_gene_id":"ENSG00000218748.1","gene_symbol":"DBIP1","gene_name":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2692]","synonyms":"DBIL2","biotype":"processed_pseudogene","ncbi_id":"1624","summary":null,"start":79436908,"end":79437167,"strand":-1,"description":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2692]"}, {"versioned_ensembl_gene_id":"ENSG00000254325.2","gene_symbol":"AC018607.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55893595,"end":55895739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176219.3","gene_symbol":"OR11H6","gene_name":"olfactory receptor family 11 subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:15349]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122748","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20223710,"end":20224702,"strand":1,"description":"olfactory receptor family 11 subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:15349]"}, {"versioned_ensembl_gene_id":"ENSG00000227689.1","gene_symbol":"SRP68P2","gene_name":"signal recognition particle 68 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30426]","synonyms":"SRPSMCR","biotype":"processed_pseudogene","ncbi_id":"252840","summary":null,"start":18527557,"end":18528461,"strand":1,"description":"signal recognition particle 68 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30426]"}, {"versioned_ensembl_gene_id":"ENSG00000224455.9","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"ARE1,SACM2L","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33420661,"end":33442416,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000006125.17","gene_symbol":"AP2B1","gene_name":"adaptor related protein complex 2 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:563]","synonyms":"CLAPB1,ADTB2","biotype":"protein_coding","ncbi_id":"163","summary":"The protein encoded by this gene is one of two large chain components of the assembly protein complex 2, which serves to link clathrin to receptors in coated vesicles. The encoded protein is found on the cytoplasmic face of coated vesicles in the plasma membrane. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":35578046,"end":35726409,"strand":1,"description":"adaptor related protein complex 2 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:563]"}, {"versioned_ensembl_gene_id":"ENSG00000225393.1","gene_symbol":"BX571846.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155468286,"end":155487046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226225.6","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"D6S218E,KE-3,S18,HKE3,KE3","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33442379,"end":33446883,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000111077.17","gene_symbol":"TNS2","gene_name":"tensin 2 [Source:HGNC Symbol;Acc:HGNC:19737]","synonyms":"TENC1,KIAA1075,C1-TEN","biotype":"protein_coding","ncbi_id":"23371","summary":"The protein encoded by this gene belongs to the tensin family. Tensin is a focal adhesion molecule that binds to actin filaments and participates in signaling pathways. This protein plays a role in regulating cell migration. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":53046969,"end":53064372,"strand":1,"description":"tensin 2 [Source:HGNC Symbol;Acc:HGNC:19737]"}, {"versioned_ensembl_gene_id":"ENSG00000139737.21","gene_symbol":"SLAIN1","gene_name":"SLAIN motif family member 1 [Source:HGNC Symbol;Acc:HGNC:26387]","synonyms":"FLJ30046,C13orf32","biotype":"protein_coding","ncbi_id":"122060","summary":null,"start":77697854,"end":77764242,"strand":1,"description":"SLAIN motif family member 1 [Source:HGNC Symbol;Acc:HGNC:26387]"}, {"versioned_ensembl_gene_id":"ENSG00000277987.1","gene_symbol":"LINC02351","gene_name":"long intergenic non-protein coding RNA 2351 [Source:HGNC Symbol;Acc:HGNC:53273]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371011","summary":null,"start":98324273,"end":98327494,"strand":-1,"description":"long intergenic non-protein coding RNA 2351 [Source:HGNC Symbol;Acc:HGNC:53273]"}, {"versioned_ensembl_gene_id":"ENSG00000233955.1","gene_symbol":"AHCYP3","gene_name":"adenosylhomocysteinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44995]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402093","summary":null,"start":104395002,"end":104396280,"strand":-1,"description":"adenosylhomocysteinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44995]"}, {"versioned_ensembl_gene_id":"ENSG00000169410.9","gene_symbol":"PTPN9","gene_name":"protein tyrosine phosphatase, non-receptor type 9 [Source:HGNC Symbol;Acc:HGNC:9661]","synonyms":"MEG2","biotype":"protein_coding","ncbi_id":"5780","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal domain that shares a significant similarity with yeast SEC14, which is a protein that has phosphatidylinositol transfer activity and is required for protein secretion through the Golgi complex in yeast. This PTP was found to be activated by polyphosphoinositide, and is thought to be involved in signaling events regulating phagocytosis. [provided by RefSeq, Jul 2008]","start":75463251,"end":75579289,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 9 [Source:HGNC Symbol;Acc:HGNC:9661]"}, {"versioned_ensembl_gene_id":"ENSG00000181698.4","gene_symbol":"OR5T1","gene_name":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]","synonyms":"OR5T1P","biotype":"protein_coding","ncbi_id":"390155","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56274154,"end":56276819,"strand":1,"description":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]"}, {"versioned_ensembl_gene_id":"ENSG00000143977.13","gene_symbol":"SNRPG","gene_name":"small nuclear ribonucleoprotein polypeptide G [Source:HGNC Symbol;Acc:HGNC:11163]","synonyms":"Sm-G","biotype":"protein_coding","ncbi_id":"6637","summary":"The protein encoded by this gene is a component of the U1, U2, U4, and U5 small nuclear ribonucleoprotein complexes, precursors of the spliceosome. The encoded protein may also be a part of the U7 small nuclear ribonucleoprotein complex, which participates in the processing of the 3' end of histone transcripts. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":70281362,"end":70293771,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G [Source:HGNC Symbol;Acc:HGNC:11163]"}, {"versioned_ensembl_gene_id":"ENSG00000107643.15","gene_symbol":"MAPK8","gene_name":"mitogen-activated protein kinase 8 [Source:HGNC Symbol;Acc:HGNC:6881]","synonyms":"JNK1,JNK,SAPK1,PRKM8","biotype":"protein_coding","ncbi_id":"5599","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various cell stimuli, and targets specific transcription factors, and thus mediates immediate-early gene expression in response to cell stimuli. The activation of this kinase by tumor-necrosis factor alpha (TNF-alpha) is found to be required for TNF-alpha induced apoptosis. This kinase is also involved in UV radiation induced apoptosis, which is thought to be related to cytochrom c-mediated cell death pathway. Studies of the mouse counterpart of this gene suggested that this kinase play a key role in T cell proliferation, apoptosis and differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Apr 2016]","start":48306639,"end":48439360,"strand":1,"description":"mitogen-activated protein kinase 8 [Source:HGNC Symbol;Acc:HGNC:6881]"}, {"versioned_ensembl_gene_id":"ENSG00000267592.1","gene_symbol":"AC004134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35596904,"end":35597128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259424.1","gene_symbol":"AC118658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98646951,"end":98647371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182022.17","gene_symbol":"CHST15","gene_name":"carbohydrate sulfotransferase 15 [Source:HGNC Symbol;Acc:HGNC:18137]","synonyms":"KIAA0598,GALNAC4S-6ST,BRAG","biotype":"protein_coding","ncbi_id":"51363","summary":"Chondroitin sulfate (CS) is a glycosaminoglycan which is an important structural component of the extracellular matrix and which links to proteins to form proteoglycans. Chondroitin sulfate E (CS-E) is an isomer of chondroitin sulfate in which the C-4 and C-6 hydroxyl groups are sulfated. This gene encodes a type II transmembrane glycoprotein that acts as a sulfotransferase to transfer sulfate to the C-6 hydroxal group of chondroitin sulfate. This gene has also been identified as being co-expressed with RAG1 in B-cells and as potentially acting as a B-cell surface signaling receptor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012]","start":124007666,"end":124093607,"strand":-1,"description":"carbohydrate sulfotransferase 15 [Source:HGNC Symbol;Acc:HGNC:18137]"}, {"versioned_ensembl_gene_id":"ENSG00000124490.13","gene_symbol":"CRISP2","gene_name":"cysteine rich secretory protein 2 [Source:HGNC Symbol;Acc:HGNC:12024]","synonyms":"TPX1,GAPDL5,CT36,CRISP-2","biotype":"protein_coding","ncbi_id":"7180","summary":null,"start":49692358,"end":49713590,"strand":-1,"description":"cysteine rich secretory protein 2 [Source:HGNC Symbol;Acc:HGNC:12024]"}, {"versioned_ensembl_gene_id":"ENSG00000215547.1","gene_symbol":"DEFB115","gene_name":"defensin beta 115 [Source:HGNC Symbol;Acc:HGNC:18096]","synonyms":"DEFB-15","biotype":"protein_coding","ncbi_id":"245929","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":31257664,"end":31259632,"strand":1,"description":"defensin beta 115 [Source:HGNC Symbol;Acc:HGNC:18096]"}, {"versioned_ensembl_gene_id":"ENSG00000260269.5","gene_symbol":"AC105036.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75527150,"end":75601205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232334.1","gene_symbol":"AL683842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124004304,"end":124004828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277112.3","gene_symbol":"ANKRD20A21P","gene_name":"ankyrin repeat domain 20 family member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:52329]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"102723552","summary":null,"start":30656033,"end":30723932,"strand":-1,"description":"ankyrin repeat domain 20 family member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:52329]"}, {"versioned_ensembl_gene_id":"ENSG00000267477.1","gene_symbol":"AC008481.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":11466240,"end":11505698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270894.1","gene_symbol":"AC015849.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":35818399,"end":35823713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213438.2","gene_symbol":"YBX2P1","gene_name":"Y-box binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100124332","summary":null,"start":123991910,"end":123992669,"strand":1,"description":"Y-box binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49498]"}, {"versioned_ensembl_gene_id":"ENSG00000254508.5","gene_symbol":"FBXO3-AS1","gene_name":"FBXO3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51147]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928440","summary":null,"start":33774699,"end":33775670,"strand":1,"description":"FBXO3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51147]"}, {"versioned_ensembl_gene_id":"ENSG00000110921.13","gene_symbol":"MVK","gene_name":"mevalonate kinase [Source:HGNC Symbol;Acc:HGNC:7530]","synonyms":"MK,LRBP","biotype":"protein_coding","ncbi_id":"4598","summary":"This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":109573255,"end":109598117,"strand":1,"description":"mevalonate kinase [Source:HGNC Symbol;Acc:HGNC:7530]"}, {"versioned_ensembl_gene_id":"ENSG00000266806.1","gene_symbol":"AC087575.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22331597,"end":22332410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214244.4","gene_symbol":"SETP21","gene_name":"SET pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100856878","summary":null,"start":60459848,"end":60460739,"strand":-1,"description":"SET pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42940]"}, {"versioned_ensembl_gene_id":"ENSG00000213303.3","gene_symbol":"AC008481.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11523436,"end":11523831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282568.1","gene_symbol":"TRBV2","gene_name":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]","synonyms":"TCRBV2S1,TCRBV22S1A2N1T","biotype":"TR_V_gene","ncbi_id":"28620","summary":null,"start":142300947,"end":142301455,"strand":1,"description":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]"}, {"versioned_ensembl_gene_id":"ENSG00000278991.1","gene_symbol":"AC090181.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77063397,"end":77064910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259652.1","gene_symbol":"AC090181.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77043680,"end":77045160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280071.3","gene_symbol":"FP565260.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5079294,"end":5128425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237515.8","gene_symbol":"SHISA9","gene_name":"shisa family member 9 [Source:HGNC Symbol;Acc:HGNC:37231]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729993","summary":null,"start":12901620,"end":13240413,"strand":1,"description":"shisa family member 9 [Source:HGNC Symbol;Acc:HGNC:37231]"}, {"versioned_ensembl_gene_id":"ENSG00000155961.4","gene_symbol":"RAB39B","gene_name":"RAB39B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16499]","synonyms":"MRX72","biotype":"protein_coding","ncbi_id":"116442","summary":"This gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking. Mutations in this gene are associated with X-linked cognitive disability. [provided by RefSeq, Aug 2013]","start":155258241,"end":155264589,"strand":-1,"description":"RAB39B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16499]"}, {"versioned_ensembl_gene_id":"ENSG00000254658.3","gene_symbol":"OR8J2","gene_name":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]","synonyms":"OR8J2P","biotype":"polymorphic_pseudogene","ncbi_id":"81169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56208985,"end":56215222,"strand":-1,"description":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]"}, {"versioned_ensembl_gene_id":"ENSG00000118292.8","gene_symbol":"C1orf54","gene_name":"chromosome 1 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26258]","synonyms":"FLJ23221","biotype":"protein_coding","ncbi_id":"79630","summary":null,"start":150268200,"end":150280916,"strand":1,"description":"chromosome 1 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26258]"}, {"versioned_ensembl_gene_id":"ENSG00000255025.1","gene_symbol":"AF228730.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7238286,"end":7238631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238200.1","gene_symbol":"MGAT2P2","gene_name":"MGAT2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422589","summary":null,"start":135751119,"end":135752583,"strand":1,"description":"MGAT2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51243]"}, {"versioned_ensembl_gene_id":"ENSG00000236844.1","gene_symbol":"AC069213.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195554610,"end":195555083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181718.6","gene_symbol":"OR5T2","gene_name":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219464","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56231282,"end":56234255,"strand":-1,"description":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]"}, {"versioned_ensembl_gene_id":"ENSG00000228929.1","gene_symbol":"RPS13P2","gene_name":"ribosomal protein S13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729236","summary":null,"start":52772194,"end":52772648,"strand":-1,"description":"ribosomal protein S13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36364]"}, {"versioned_ensembl_gene_id":"ENSG00000269096.6","gene_symbol":"CT45A3","gene_name":"cancer/testis antigen family 45 member A3 [Source:HGNC Symbol;Acc:HGNC:33268]","synonyms":"CT45A4,CT45.4,CT45.3,CT45-4,CT45-3","biotype":"protein_coding","ncbi_id":"441519","summary":null,"start":135759846,"end":135768191,"strand":-1,"description":"cancer/testis antigen family 45 member A3 [Source:HGNC Symbol;Acc:HGNC:33268]"}, {"versioned_ensembl_gene_id":"ENSG00000225008.1","gene_symbol":"AC234781.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155290360,"end":155291353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231319.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR6-4,OR2B3P","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086272,"end":29087278,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000228986.1","gene_symbol":"AC234781.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155292169,"end":155293432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247345.2","gene_symbol":"AC092343.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59039761,"end":59063503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230491.1","gene_symbol":"AC234781.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155310247,"end":155310490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155962.12","gene_symbol":"CLIC2","gene_name":"chloride intracellular channel 2 [Source:HGNC Symbol;Acc:HGNC:2063]","synonyms":"XAP121","biotype":"protein_coding","ncbi_id":"1193","summary":"This gene encodes a chloride intracellular channel protein. Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. This protein plays a role in inhibiting the function of ryanodine receptor 2. A mutation in this gene is the cause of an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017]","start":155276211,"end":155334657,"strand":-1,"description":"chloride intracellular channel 2 [Source:HGNC Symbol;Acc:HGNC:2063]"}, {"versioned_ensembl_gene_id":"ENSG00000262116.1","gene_symbol":"AC009134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13197606,"end":13204907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152931.7","gene_symbol":"PART1","gene_name":"prostate androgen-regulated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17263]","synonyms":"NCRNA00206,DKFZP586D0823","biotype":"lincRNA","ncbi_id":"25859","summary":"This gene is induced by androgen in prostate adenocarcinoma cells. Multiple alternatively transcript variants have been described for this gene, none of which are predicted to encode a protein product. [provided by RefSeq, Sep 2009]","start":60487713,"end":60547657,"strand":1,"description":"prostate androgen-regulated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17263]"}, {"versioned_ensembl_gene_id":"ENSG00000161914.9","gene_symbol":"ZNF653","gene_name":"zinc finger protein 653 [Source:HGNC Symbol;Acc:HGNC:25196]","synonyms":"Zip67","biotype":"protein_coding","ncbi_id":"115950","summary":null,"start":11483427,"end":11505923,"strand":-1,"description":"zinc finger protein 653 [Source:HGNC Symbol;Acc:HGNC:25196]"}, {"versioned_ensembl_gene_id":"ENSG00000279137.1","gene_symbol":"AL356309.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126518840,"end":126520773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226078.1","gene_symbol":"AL356309.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126527618,"end":126530343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230227.4","gene_symbol":"SIAH1P1","gene_name":"siah E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30966]","synonyms":"SIAH1L","biotype":"processed_pseudogene","ncbi_id":"340571","summary":null,"start":35626142,"end":35627064,"strand":1,"description":"siah E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30966]"}, {"versioned_ensembl_gene_id":"ENSG00000212330.1","gene_symbol":"RNU6-244P","gene_name":"RNA, U6 small nuclear 244, pseudogene [Source:HGNC Symbol;Acc:HGNC:47207]","synonyms":null,"biotype":"snRNA","ncbi_id":"106866981","summary":null,"start":102501676,"end":102501779,"strand":1,"description":"RNA, U6 small nuclear 244, pseudogene [Source:HGNC Symbol;Acc:HGNC:47207]"}, {"versioned_ensembl_gene_id":"ENSG00000207171.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":168471409,"end":168471539,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000264960.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32579248,"end":32579395,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000212442.1","gene_symbol":"RNU6-243P","gene_name":"RNA, U6 small nuclear 243, pseudogene [Source:HGNC Symbol;Acc:HGNC:47206]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479675","summary":null,"start":35256840,"end":35256946,"strand":-1,"description":"RNA, U6 small nuclear 243, pseudogene [Source:HGNC Symbol;Acc:HGNC:47206]"}, {"versioned_ensembl_gene_id":"ENSG00000278144.1","gene_symbol":"NEAT1_1","gene_name":"Nuclear enriched abundant transcript 1 conserved region 1 [Source:RFAM;Acc:RF01955]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423273,"end":65423392,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 1 [Source:RFAM;Acc:RF01955]"}, {"versioned_ensembl_gene_id":"ENSG00000283926.1","gene_symbol":"MIR192","gene_name":"microRNA 192 [Source:HGNC Symbol;Acc:HGNC:31562]","synonyms":"MIRN192,hsa-mir-192","biotype":"miRNA","ncbi_id":"406967","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64891137,"end":64891246,"strand":-1,"description":"microRNA 192 [Source:HGNC Symbol;Acc:HGNC:31562]"}, {"versioned_ensembl_gene_id":"ENSG00000207940.1","gene_symbol":"MIR567","gene_name":"microRNA 567 [Source:HGNC Symbol;Acc:HGNC:32823]","synonyms":"MIRN567,hsa-mir-567","biotype":"miRNA","ncbi_id":"693152","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112112801,"end":112112898,"strand":1,"description":"microRNA 567 [Source:HGNC Symbol;Acc:HGNC:32823]"}, {"versioned_ensembl_gene_id":"ENSG00000221502.1","gene_symbol":"MIR1245A","gene_name":"microRNA 1245a [Source:HGNC Symbol;Acc:HGNC:35311]","synonyms":"MIR1245,hsa-mir-1245,MIRN1245","biotype":"miRNA","ncbi_id":"100302219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188978092,"end":188978161,"strand":1,"description":"microRNA 1245a [Source:HGNC Symbol;Acc:HGNC:35311]"}, {"versioned_ensembl_gene_id":"ENSG00000215952.1","gene_symbol":"MIR921","gene_name":"microRNA 921 [Source:HGNC Symbol;Acc:HGNC:33671]","synonyms":"MIRN921,hsa-mir-921","biotype":"miRNA","ncbi_id":"100126349","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":166154743,"end":166154798,"strand":-1,"description":"microRNA 921 [Source:HGNC Symbol;Acc:HGNC:33671]"}, {"versioned_ensembl_gene_id":"ENSG00000278549.1","gene_symbol":"MIR6736","gene_name":"microRNA 6736 [Source:HGNC Symbol;Acc:HGNC:50072]","synonyms":"hsa-mir-6736","biotype":"miRNA","ncbi_id":"102466191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145850587,"end":145850645,"strand":-1,"description":"microRNA 6736 [Source:HGNC Symbol;Acc:HGNC:50072]"}, {"versioned_ensembl_gene_id":"ENSG00000252303.2","gene_symbol":"RNU6-280P","gene_name":"RNA, U6 small nuclear 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:47243]","synonyms":"RNU6-1221P","biotype":"snRNA","ncbi_id":"106481886","summary":null,"start":67546651,"end":67546754,"strand":1,"description":"RNA, U6 small nuclear 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:47243]"}, {"versioned_ensembl_gene_id":"ENSG00000223190.1","gene_symbol":"RN7SKP100","gene_name":"RNA, 7SK small nuclear pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:45824]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479139","summary":null,"start":43063326,"end":43063609,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:45824]"}, {"versioned_ensembl_gene_id":"ENSG00000274208.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":189720125,"end":189720300,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000221698.1","gene_symbol":"MIR548H3","gene_name":"microRNA 548h-3 [Source:HGNC Symbol;Acc:HGNC:35344]","synonyms":"MIRN548H3,hsa-mir-548h-3","biotype":"miRNA","ncbi_id":"100302287","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13543529,"end":13543646,"strand":-1,"description":"microRNA 548h-3 [Source:HGNC Symbol;Acc:HGNC:35344]"}, {"versioned_ensembl_gene_id":"ENSG00000266886.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31360234,"end":31360340,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000239471.3","gene_symbol":"RN7SL584P","gene_name":"RNA, 7SL, cytoplasmic 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:46600]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480519","summary":null,"start":20095733,"end":20096029,"strand":-1,"description":"RNA, 7SL, cytoplasmic 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:46600]"}, {"versioned_ensembl_gene_id":"ENSG00000206939.1","gene_symbol":"RNU6-281P","gene_name":"RNA, U6 small nuclear 281, pseudogene [Source:HGNC 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processing and modification. snoRNAs of the box C/D class, like SNORD83B, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39313819,"end":39313911,"strand":-1,"description":"small nucleolar RNA, C/D box 83B [Source:HGNC Symbol;Acc:HGNC:17132]"}, {"versioned_ensembl_gene_id":"ENSG00000252595.1","gene_symbol":"RN7SKP82","gene_name":"RNA, 7SK small nuclear pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:45806]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480462","summary":null,"start":42892396,"end":42892618,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:45806]"}, {"versioned_ensembl_gene_id":"ENSG00000278007.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":4127492,"end":4127732,"strand":1,"description":"Metazoan signal recognition 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{"versioned_ensembl_gene_id":"ENSG00000212135.1","gene_symbol":"SNORD67","gene_name":"small nucleolar RNA, C/D box 67 [Source:HGNC Symbol;Acc:HGNC:32728]","synonyms":"HBII-166","biotype":"snoRNA","ncbi_id":"692108","summary":null,"start":46762389,"end":46762499,"strand":-1,"description":"small nucleolar RNA, C/D box 67 [Source:HGNC Symbol;Acc:HGNC:32728]"}, {"versioned_ensembl_gene_id":"ENSG00000207187.1","gene_symbol":"SNORA10B","gene_name":"small nucleolar RNA, H/ACA box 10B [Source:HGNC Symbol;Acc:HGNC:52188]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616960","summary":null,"start":30187434,"end":30187566,"strand":1,"description":"small nucleolar RNA, H/ACA box 10B [Source:HGNC Symbol;Acc:HGNC:52188]"}, {"versioned_ensembl_gene_id":"ENSG00000200827.1","gene_symbol":"RNU6-324P","gene_name":"RNA, U6 small nuclear 324, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000212260.1","gene_symbol":"RNU6-724P","gene_name":"RNA, U6 small nuclear 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:47687]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479887","summary":null,"start":69530613,"end":69530717,"strand":-1,"description":"RNA, U6 small nuclear 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:47687]"}, {"versioned_ensembl_gene_id":"ENSG00000242020.3","gene_symbol":"RN7SL68P","gene_name":"RNA, 7SL, cytoplasmic 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:46084]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080632","summary":null,"start":141479316,"end":141479625,"strand":1,"description":"RNA, 7SL, cytoplasmic 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:46084]"}, {"versioned_ensembl_gene_id":"ENSG00000200487.1","gene_symbol":"RNA5SP322","gene_name":"RNA, 5S ribosomal pseudogene 322 [Source:HGNC 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Box H/ACA snoRNAs, such as SNORA5C, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":45104906,"end":45105042,"strand":-1,"description":"small nucleolar RNA, H/ACA box 5C [Source:HGNC Symbol;Acc:HGNC:32590]"}, {"versioned_ensembl_gene_id":"ENSG00000202141.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":183022859,"end":183022971,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265733.1","gene_symbol":"SNORA74C-1","gene_name":"small nucleolar RNA, H/ACA box 74C-1 [Source:HGNC Symbol;Acc:HGNC:52217]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616974","summary":null,"start":45984610,"end":45984810,"strand":1,"description":"small nucleolar RNA, H/ACA box 74C-1 [Source:HGNC Symbol;Acc:HGNC:52217]"}, 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{"versioned_ensembl_gene_id":"ENSG00000223142.1","gene_symbol":"RN7SKP252","gene_name":"RNA, 7SK small nuclear pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:45976]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479207","summary":null,"start":49738677,"end":49739003,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:45976]"}, {"versioned_ensembl_gene_id":"ENSG00000200674.1","gene_symbol":"RN7SKP160","gene_name":"RNA, 7SK small nuclear pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:45884]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479166","summary":null,"start":173791548,"end":173791887,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:45884]"}, {"versioned_ensembl_gene_id":"ENSG00000206613.1","gene_symbol":"RNU6-1336P","gene_name":"RNA, U6 small nuclear 1336, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000283694.1","gene_symbol":"MIR3202-2","gene_name":"microRNA 3202-2 [Source:HGNC Symbol;Acc:HGNC:38228]","synonyms":"hsa-mir-3202-2","biotype":"miRNA","ncbi_id":"100422877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153981098,"end":153981176,"strand":-1,"description":"microRNA 3202-2 [Source:HGNC Symbol;Acc:HGNC:38228]"}, {"versioned_ensembl_gene_id":"ENSG00000252171.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45047103,"end":45047215,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271886.1","gene_symbol":"MIR98","gene_name":"microRNA 98 [Source:HGNC Symbol;Acc:HGNC:31649]","synonyms":"MIRN98,hsa-mir-98","biotype":"miRNA","ncbi_id":"407054","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53556223,"end":53556341,"strand":-1,"description":"microRNA 98 [Source:HGNC Symbol;Acc:HGNC:31649]"}, {"versioned_ensembl_gene_id":"ENSG00000199960.1","gene_symbol":"SNORD115-14","gene_name":"small nucleolar RNA, C/D box 115-14 [Source:HGNC Symbol;Acc:HGNC:33033]","synonyms":"HBII-52-14","biotype":"snoRNA","ncbi_id":"100033451","summary":null,"start":25194921,"end":25195001,"strand":1,"description":"small nucleolar RNA, C/D box 115-14 [Source:HGNC Symbol;Acc:HGNC:33033]"}, {"versioned_ensembl_gene_id":"ENSG00000252903.2","gene_symbol":"RNU6-894P","gene_name":"RNA, U6 small nuclear 894, pseudogene [Source:HGNC Symbol;Acc:HGNC:47857]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481461","summary":null,"start":31348192,"end":31348296,"strand":1,"description":"RNA, U6 small nuclear 894, pseudogene [Source:HGNC Symbol;Acc:HGNC:47857]"}, {"versioned_ensembl_gene_id":"ENSG00000241152.3","gene_symbol":"RN7SL720P","gene_name":"RNA, 7SL, cytoplasmic 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:46736]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480528","summary":null,"start":17053901,"end":17054204,"strand":1,"description":"RNA, 7SL, cytoplasmic 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:46736]"}, {"versioned_ensembl_gene_id":"ENSG00000207804.1","gene_symbol":"MIR599","gene_name":"microRNA 599 [Source:HGNC Symbol;Acc:HGNC:32855]","synonyms":"hsa-mir-599,MIRN599","biotype":"miRNA","ncbi_id":"693184","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99536636,"end":99536730,"strand":-1,"description":"microRNA 599 [Source:HGNC Symbol;Acc:HGNC:32855]"}, {"versioned_ensembl_gene_id":"ENSG00000206654.1","gene_symbol":"RNU6-608P","gene_name":"RNA, U6 small nuclear 608, pseudogene [Source:HGNC Symbol;Acc:HGNC:47571]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481373","summary":null,"start":39120940,"end":39121043,"strand":-1,"description":"RNA, U6 small nuclear 608, pseudogene [Source:HGNC Symbol;Acc:HGNC:47571]"}, {"versioned_ensembl_gene_id":"ENSG00000252657.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":29777619,"end":29777744,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000275362.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18615581,"end":18615900,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252436.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62726636,"end":62726740,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264706.2","gene_symbol":"RN7SL217P","gene_name":"RNA, 7SL, cytoplasmic 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:46233]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479301","summary":null,"start":49863375,"end":49863660,"strand":-1,"description":"RNA, 7SL, cytoplasmic 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:46233]"}, {"versioned_ensembl_gene_id":"ENSG00000212336.1","gene_symbol":"RNA5SP210","gene_name":"RNA, 5S ribosomal pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:43110]","synonyms":"RN5S210","biotype":"rRNA","ncbi_id":"100873470","summary":null,"start":81622200,"end":81622319,"strand":1,"description":"RNA, 5S ribosomal pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:43110]"}, {"versioned_ensembl_gene_id":"ENSG00000251929.1","gene_symbol":"RNU6-189P","gene_name":"RNA, U6 small nuclear 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:47152]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479650","summary":null,"start":49901850,"end":49901950,"strand":-1,"description":"RNA, U6 small nuclear 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:47152]"}, {"versioned_ensembl_gene_id":"ENSG00000278048.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43251829,"end":43252019,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000200118.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":170244782,"end":170244881,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284266.1","gene_symbol":"MIR4534","gene_name":"microRNA 4534 [Source:HGNC Symbol;Acc:HGNC:41692]","synonyms":"hsa-mir-4534","biotype":"miRNA","ncbi_id":"100616146","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37988794,"end":37988853,"strand":1,"description":"microRNA 4534 [Source:HGNC Symbol;Acc:HGNC:41692]"}, {"versioned_ensembl_gene_id":"ENSG00000199398.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":160008445,"end":160008546,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200026.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":38147428,"end":38147561,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000284256.1","gene_symbol":"MIR5004","gene_name":"microRNA 5004 [Source:HGNC Symbol;Acc:HGNC:43532]","synonyms":"hsa-mir-5004","biotype":"miRNA","ncbi_id":"100847012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33438331,"end":33438437,"strand":1,"description":"microRNA 5004 [Source:HGNC Symbol;Acc:HGNC:43532]"}, {"versioned_ensembl_gene_id":"ENSG00000240803.3","gene_symbol":"RN7SL231P","gene_name":"RNA, 7SL, cytoplasmic 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:46247]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480984","summary":null,"start":14213052,"end":14213323,"strand":1,"description":"RNA, 7SL, cytoplasmic 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:46247]"}, {"versioned_ensembl_gene_id":"ENSG00000284325.1","gene_symbol":"MIR3655","gene_name":"microRNA 3655 [Source:HGNC Symbol;Acc:HGNC:38960]","synonyms":"hsa-mir-3655","biotype":"miRNA","ncbi_id":"100500820","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140647844,"end":140647926,"strand":1,"description":"microRNA 3655 [Source:HGNC Symbol;Acc:HGNC:38960]"}, {"versioned_ensembl_gene_id":"ENSG00000200545.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":19598247,"end":19598463,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000206764.1","gene_symbol":"RNU6-152P","gene_name":"RNA, U6 small nuclear 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:47115]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481223","summary":null,"start":182327068,"end":182327174,"strand":1,"description":"RNA, U6 small nuclear 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:47115]"}, {"versioned_ensembl_gene_id":"ENSG00000264999.1","gene_symbol":"MIR5089","gene_name":"microRNA 5089 [Source:HGNC Symbol;Acc:HGNC:43536]","synonyms":"hsa-mir-5089","biotype":"miRNA","ncbi_id":"100847067","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46973017,"end":46973100,"strand":1,"description":"microRNA 5089 [Source:HGNC Symbol;Acc:HGNC:43536]"}, {"versioned_ensembl_gene_id":"ENSG00000284082.1","gene_symbol":"MIR7109","gene_name":"microRNA 7109 [Source:HGNC Symbol;Acc:HGNC:50122]","synonyms":"hsa-mir-7109","biotype":"miRNA","ncbi_id":"102465666","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31621467,"end":31621531,"strand":-1,"description":"microRNA 7109 [Source:HGNC Symbol;Acc:HGNC:50122]"}, {"versioned_ensembl_gene_id":"ENSG00000277864.1","gene_symbol":"SCARNA15","gene_name":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]","synonyms":"ACA45,ACA45","biotype":"scaRNA","ncbi_id":"677778","summary":null,"start":82755945,"end":82756071,"strand":1,"description":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]"}, {"versioned_ensembl_gene_id":"ENSG00000238498.1","gene_symbol":"SNORD13P1","gene_name":"small nucleolar RNA, C/D box 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10110]","synonyms":"U13.32A,U13,RNU13P1","biotype":"snoRNA","ncbi_id":"6076","summary":null,"start":42076058,"end":42076161,"strand":-1,"description":"small nucleolar RNA, C/D box 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10110]"}, {"versioned_ensembl_gene_id":"ENSG00000207318.1","gene_symbol":"RNU6-1184P","gene_name":"RNA, U6 small nuclear 1184, pseudogene [Source:HGNC Symbol;Acc:HGNC:48147]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481553","summary":null,"start":147831770,"end":147831877,"strand":1,"description":"RNA, U6 small nuclear 1184, pseudogene [Source:HGNC Symbol;Acc:HGNC:48147]"}, {"versioned_ensembl_gene_id":"ENSG00000223019.1","gene_symbol":"RNA5SP306","gene_name":"RNA, 5S ribosomal pseudogene 306 [Source:HGNC Symbol;Acc:HGNC:43206]","synonyms":"RN5S306","biotype":"rRNA","ncbi_id":"100873580","summary":null,"start":25813811,"end":25813917,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 306 [Source:HGNC Symbol;Acc:HGNC:43206]"}, {"versioned_ensembl_gene_id":"ENSG00000238749.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61883640,"end":61883751,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283301.1","gene_symbol":"MIR4520-2","gene_name":"microRNA 4520-2 [Source:HGNC Symbol;Acc:HGNC:41839]","synonyms":"MIR4520B,hsa-mir-4520b","biotype":"miRNA","ncbi_id":"100616466","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6655449,"end":6655502,"strand":1,"description":"microRNA 4520-2 [Source:HGNC Symbol;Acc:HGNC:41839]"}, {"versioned_ensembl_gene_id":"ENSG00000253000.1","gene_symbol":"RNU1-45P","gene_name":"RNA, U1 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:48387]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481610","summary":null,"start":178116721,"end":178116861,"strand":-1,"description":"RNA, U1 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:48387]"}, {"versioned_ensembl_gene_id":"ENSG00000264796.1","gene_symbol":"MIR5009","gene_name":"microRNA 5009 [Source:HGNC Symbol;Acc:HGNC:43458]","synonyms":"hsa-mir-5009","biotype":"miRNA","ncbi_id":"100846993","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89883931,"end":89884030,"strand":-1,"description":"microRNA 5009 [Source:HGNC Symbol;Acc:HGNC:43458]"}, {"versioned_ensembl_gene_id":"ENSG00000207094.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"RNU67,U67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":88449092,"end":88449231,"strand":-1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000265003.1","gene_symbol":"MIR4780","gene_name":"microRNA 4780 [Source:HGNC Symbol;Acc:HGNC:41552]","synonyms":"hsa-mir-4780","biotype":"miRNA","ncbi_id":"100616447","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88082519,"end":88082599,"strand":-1,"description":"microRNA 4780 [Source:HGNC Symbol;Acc:HGNC:41552]"}, {"versioned_ensembl_gene_id":"ENSG00000278236.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87184849,"end":87185020,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000207579.1","gene_symbol":"MIR662","gene_name":"microRNA 662 [Source:HGNC Symbol;Acc:HGNC:32918]","synonyms":"MIRN662,hsa-mir-662","biotype":"miRNA","ncbi_id":"724032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":770183,"end":770277,"strand":1,"description":"microRNA 662 [Source:HGNC Symbol;Acc:HGNC:32918]"}, {"versioned_ensembl_gene_id":"ENSG00000252254.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8328067,"end":8328179,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201044.1","gene_symbol":"RNU6-268P","gene_name":"RNA, U6 small nuclear 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:47231]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479685","summary":null,"start":230752141,"end":230752247,"strand":1,"description":"RNA, U6 small nuclear 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:47231]"}, {"versioned_ensembl_gene_id":"ENSG00000283881.1","gene_symbol":"MIR3916","gene_name":"microRNA 3916 [Source:HGNC Symbol;Acc:HGNC:38912]","synonyms":"hsa-mir-3916","biotype":"miRNA","ncbi_id":"100500849","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":247201967,"end":247202060,"strand":-1,"description":"microRNA 3916 [Source:HGNC Symbol;Acc:HGNC:38912]"}, {"versioned_ensembl_gene_id":"ENSG00000201733.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":66432763,"end":66432902,"strand":1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000239005.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":139436368,"end":139436494,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000243505.3","gene_symbol":"RN7SL240P","gene_name":"RNA, 7SL, cytoplasmic 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:46256]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479310","summary":null,"start":29721399,"end":29721684,"strand":-1,"description":"RNA, 7SL, cytoplasmic 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:46256]"}, {"versioned_ensembl_gene_id":"ENSG00000252661.1","gene_symbol":"RNU6-782P","gene_name":"RNA, U6 small nuclear 782, pseudogene [Source:HGNC Symbol;Acc:HGNC:47745]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481917","summary":null,"start":15145215,"end":15145318,"strand":1,"description":"RNA, U6 small nuclear 782, pseudogene [Source:HGNC Symbol;Acc:HGNC:47745]"}, {"versioned_ensembl_gene_id":"ENSG00000252684.1","gene_symbol":"RNU6ATAC36P","gene_name":"RNA, U6atac small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46935]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480543","summary":null,"start":76948791,"end":76948870,"strand":1,"description":"RNA, U6atac small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46935]"}, {"versioned_ensembl_gene_id":"ENSG00000283789.1","gene_symbol":"MIR7846","gene_name":"microRNA 7846 [Source:HGNC Symbol;Acc:HGNC:50029]","synonyms":"hsa-mir-7846","biotype":"miRNA","ncbi_id":"102465836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12166943,"end":12167038,"strand":1,"description":"microRNA 7846 [Source:HGNC Symbol;Acc:HGNC:50029]"}, {"versioned_ensembl_gene_id":"ENSG00000202151.1","gene_symbol":"RNY4P28","gene_name":"RNA, Ro-associated Y4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42496]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873822","summary":null,"start":60187738,"end":60187830,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42496]"}, {"versioned_ensembl_gene_id":"ENSG00000277311.1","gene_symbol":"Six3os1_2","gene_name":"Six3os1 conserved region 2 [Source:RFAM;Acc:RF02247]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44934055,"end":44934271,"strand":1,"description":"Six3os1 conserved region 2 [Source:RFAM;Acc:RF02247]"}, {"versioned_ensembl_gene_id":"ENSG00000201113.1","gene_symbol":"RNU6-647P","gene_name":"RNA, U6 small nuclear 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:47610]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480598","summary":null,"start":32214456,"end":32214562,"strand":-1,"description":"RNA, U6 small nuclear 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:47610]"}, {"versioned_ensembl_gene_id":"ENSG00000239899.3","gene_symbol":"RN7SL674P","gene_name":"RNA, 7SL, cytoplasmic 674, pseudogene [Source:HGNC Symbol;Acc:HGNC:46690]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479468","summary":null,"start":11584773,"end":11585047,"strand":1,"description":"RNA, 7SL, cytoplasmic 674, pseudogene [Source:HGNC Symbol;Acc:HGNC:46690]"}, {"versioned_ensembl_gene_id":"ENSG00000251971.1","gene_symbol":"RNU6-1333P","gene_name":"RNA, U6 small nuclear 1333, pseudogene [Source:HGNC Symbol;Acc:HGNC:48296]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481601","summary":null,"start":238028971,"end":238029063,"strand":-1,"description":"RNA, U6 small nuclear 1333, pseudogene [Source:HGNC Symbol;Acc:HGNC:48296]"}, {"versioned_ensembl_gene_id":"ENSG00000201444.1","gene_symbol":"RNU6-1082P","gene_name":"RNA, U6 small nuclear 1082, pseudogene [Source:HGNC Symbol;Acc:HGNC:48045]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480041","summary":null,"start":117707996,"end":117708102,"strand":-1,"description":"RNA, U6 small nuclear 1082, pseudogene [Source:HGNC Symbol;Acc:HGNC:48045]"}, {"versioned_ensembl_gene_id":"ENSG00000275021.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868796,"end":54868902,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000238724.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":114527129,"end":114527232,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000242565.3","gene_symbol":"RN7SL372P","gene_name":"RNA, 7SL, cytoplasmic 372, pseudogene [Source:HGNC Symbol;Acc:HGNC:46388]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479358","summary":null,"start":153704088,"end":153704385,"strand":1,"description":"RNA, 7SL, cytoplasmic 372, pseudogene [Source:HGNC Symbol;Acc:HGNC:46388]"}, {"versioned_ensembl_gene_id":"ENSG00000212270.1","gene_symbol":"SNORD37","gene_name":"Small nucleolar RNA SNORD37 [Source:RFAM;Acc:RF00440]","synonyms":"U37,RNU37","biotype":"snoRNA","ncbi_id":"26812","summary":null,"start":25806648,"end":25806712,"strand":-1,"description":"Small nucleolar RNA SNORD37 [Source:RFAM;Acc:RF00440]"}, {"versioned_ensembl_gene_id":"ENSG00000239142.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":5093408,"end":5093543,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000274078.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34,SEN34L,SEN34L,LENG5,LENG5,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000276442.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":144265217,"end":144265326,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000252845.1","gene_symbol":"RNA5SP101","gene_name":"RNA, 5S ribosomal pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:42899]","synonyms":"RN5S101","biotype":"rRNA","ncbi_id":"100873372","summary":null,"start":96956708,"end":96956815,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:42899]"}, {"versioned_ensembl_gene_id":"ENSG00000277591.1","gene_symbol":"RN7SL575P","gene_name":"RNA, 7SL, cytoplasmic 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:46591]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479432","summary":null,"start":95003545,"end":95003843,"strand":-1,"description":"RNA, 7SL, cytoplasmic 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:46591]"}, {"versioned_ensembl_gene_id":"ENSG00000239690.3","gene_symbol":"RN7SL668P","gene_name":"RNA, 7SL, cytoplasmic 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:46684]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479466","summary":null,"start":234904186,"end":234904488,"strand":1,"description":"RNA, 7SL, cytoplasmic 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:46684]"}, {"versioned_ensembl_gene_id":"ENSG00000207155.1","gene_symbol":"RNY1P14","gene_name":"RNA, Ro-associated Y1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50877]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480311","summary":null,"start":140700835,"end":140700942,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50877]"}, {"versioned_ensembl_gene_id":"ENSG00000238950.1","gene_symbol":"RNU7-173P","gene_name":"RNA, U7 small nuclear 173 pseudogene [Source:HGNC Symbol;Acc:HGNC:45707]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479090","summary":null,"start":47826969,"end":47827044,"strand":-1,"description":"RNA, U7 small nuclear 173 pseudogene [Source:HGNC Symbol;Acc:HGNC:45707]"}, {"versioned_ensembl_gene_id":"ENSG00000242818.3","gene_symbol":"RN7SL846P","gene_name":"RNA, 7SL, cytoplasmic 846, pseudogene [Source:HGNC Symbol;Acc:HGNC:46862]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479530","summary":null,"start":119768247,"end":119768538,"strand":1,"description":"RNA, 7SL, cytoplasmic 846, pseudogene [Source:HGNC Symbol;Acc:HGNC:46862]"}, {"versioned_ensembl_gene_id":"ENSG00000240940.3","gene_symbol":"RN7SL591P","gene_name":"RNA, 7SL, cytoplasmic 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:46607]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481084","summary":null,"start":62350006,"end":62350297,"strand":1,"description":"RNA, 7SL, cytoplasmic 591, pseudogene [Source:HGNC Symbol;Acc:HGNC:46607]"}, {"versioned_ensembl_gene_id":"ENSG00000251778.1","gene_symbol":"SNORA3","gene_name":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":41882205,"end":41882300,"strand":1,"description":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]"}, {"versioned_ensembl_gene_id":"ENSG00000283931.1","gene_symbol":"MIR18B","gene_name":"microRNA 18b [Source:HGNC Symbol;Acc:HGNC:32025]","synonyms":"MIRN18B,hsa-mir-18b","biotype":"miRNA","ncbi_id":"574033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134170041,"end":134170111,"strand":-1,"description":"microRNA 18b [Source:HGNC Symbol;Acc:HGNC:32025]"}, {"versioned_ensembl_gene_id":"ENSG00000202334.1","gene_symbol":"RNA5SP238","gene_name":"RNA, 5S ribosomal pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:43138]","synonyms":"RN5S238","biotype":"rRNA","ncbi_id":"100873496","summary":null,"start":114613787,"end":114613906,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 238 [Source:HGNC Symbol;Acc:HGNC:43138]"}, {"versioned_ensembl_gene_id":"ENSG00000253437.1","gene_symbol":"RNU6-988P","gene_name":"RNA, U6 small nuclear 988, pseudogene [Source:HGNC Symbol;Acc:HGNC:47951]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480003","summary":null,"start":38122374,"end":38122480,"strand":1,"description":"RNA, U6 small nuclear 988, pseudogene [Source:HGNC Symbol;Acc:HGNC:47951]"}, {"versioned_ensembl_gene_id":"ENSG00000266017.1","gene_symbol":"MIR4477B","gene_name":"microRNA 4477b [Source:HGNC Symbol;Acc:HGNC:41898]","synonyms":"hsa-mir-4477b","biotype":"miRNA","ncbi_id":"100616194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63819574,"end":63819654,"strand":1,"description":"microRNA 4477b [Source:HGNC Symbol;Acc:HGNC:41898]"}, {"versioned_ensembl_gene_id":"ENSG00000201775.1","gene_symbol":"RNU6-1325P","gene_name":"RNA, U6 small nuclear 1325, pseudogene [Source:HGNC Symbol;Acc:HGNC:48288]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480145","summary":null,"start":59834063,"end":59834167,"strand":1,"description":"RNA, U6 small nuclear 1325, pseudogene [Source:HGNC Symbol;Acc:HGNC:48288]"}, {"versioned_ensembl_gene_id":"ENSG00000275889.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264566,"end":54264668,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000263533.1","gene_symbol":"MIR4463","gene_name":"microRNA 4463 [Source:HGNC Symbol;Acc:HGNC:41665]","synonyms":"hsa-mir-4463","biotype":"miRNA","ncbi_id":"100616389","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75428407,"end":75428473,"strand":1,"description":"microRNA 4463 [Source:HGNC Symbol;Acc:HGNC:41665]"}, {"versioned_ensembl_gene_id":"ENSG00000284469.1","gene_symbol":"MIR6721","gene_name":"microRNA 6721 [Source:HGNC Symbol;Acc:HGNC:50049]","synonyms":"hsa-mir-6721","biotype":"miRNA","ncbi_id":"102466190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32170030,"end":32170116,"strand":-1,"description":"microRNA 6721 [Source:HGNC Symbol;Acc:HGNC:50049]"}, {"versioned_ensembl_gene_id":"ENSG00000265846.1","gene_symbol":"MIR4276","gene_name":"microRNA 4276 [Source:HGNC Symbol;Acc:HGNC:38232]","synonyms":"hsa-mir-4276","biotype":"miRNA","ncbi_id":"100423042","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":174423795,"end":174423864,"strand":1,"description":"microRNA 4276 [Source:HGNC Symbol;Acc:HGNC:38232]"}, {"versioned_ensembl_gene_id":"ENSG00000207399.1","gene_symbol":"RNU6-1011P","gene_name":"RNA, U6 small nuclear 1011, pseudogene [Source:HGNC Symbol;Acc:HGNC:47974]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480011","summary":null,"start":103384961,"end":103385067,"strand":1,"description":"RNA, U6 small nuclear 1011, pseudogene [Source:HGNC Symbol;Acc:HGNC:47974]"}, {"versioned_ensembl_gene_id":"ENSG00000266518.1","gene_symbol":"MIR4268","gene_name":"microRNA 4268 [Source:HGNC Symbol;Acc:HGNC:38352]","synonyms":"hsa-mir-4268","biotype":"miRNA","ncbi_id":"100422959","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219906502,"end":219906565,"strand":-1,"description":"microRNA 4268 [Source:HGNC Symbol;Acc:HGNC:38352]"}, {"versioned_ensembl_gene_id":"ENSG00000239183.1","gene_symbol":"SNORA84","gene_name":"small nucleolar RNA, H/ACA box 84 [Source:HGNC Symbol;Acc:HGNC:33615]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124534","summary":null,"start":92292461,"end":92292593,"strand":-1,"description":"small nucleolar RNA, H/ACA box 84 [Source:HGNC Symbol;Acc:HGNC:33615]"}, {"versioned_ensembl_gene_id":"ENSG00000222397.1","gene_symbol":"RN7SKP229","gene_name":"RNA, 7SK small nuclear pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:45953]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480904","summary":null,"start":181839473,"end":181839774,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:45953]"}, {"versioned_ensembl_gene_id":"ENSG00000212190.1","gene_symbol":"RNU6-298P","gene_name":"RNA, U6 small nuclear 298, pseudogene [Source:HGNC Symbol;Acc:HGNC:47261]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481273","summary":null,"start":30861843,"end":30861938,"strand":1,"description":"RNA, U6 small nuclear 298, pseudogene [Source:HGNC Symbol;Acc:HGNC:47261]"}, {"versioned_ensembl_gene_id":"ENSG00000206717.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34821445,"end":34821542,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201943.1","gene_symbol":"SNORD115-10","gene_name":"small nucleolar RNA, C/D box 115-10 [Source:HGNC Symbol;Acc:HGNC:33029]","synonyms":"HBII-52-10","biotype":"snoRNA","ncbi_id":"100033447","summary":null,"start":25187536,"end":25187616,"strand":1,"description":"small nucleolar RNA, C/D box 115-10 [Source:HGNC Symbol;Acc:HGNC:33029]"}, {"versioned_ensembl_gene_id":"ENSG00000264557.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32429038,"end":32429144,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000267611.1","gene_symbol":"AC008521.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33051515,"end":33051701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259655.1","gene_symbol":"AC090825.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99791127,"end":99792847,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263872.1","gene_symbol":"MIR4528","gene_name":"microRNA 4528 [Source:HGNC Symbol;Acc:HGNC:41547]","synonyms":"hsa-mir-4528","biotype":"miRNA","ncbi_id":"100616232","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53237101,"end":53237190,"strand":1,"description":"microRNA 4528 [Source:HGNC Symbol;Acc:HGNC:41547]"}, {"versioned_ensembl_gene_id":"ENSG00000251815.1","gene_symbol":"SNORD116-26","gene_name":"small nucleolar RNA, C/D box 116-26 [Source:HGNC Symbol;Acc:HGNC:33092]","synonyms":"HBII-85-26","biotype":"snoRNA","ncbi_id":"100033438","summary":null,"start":25099499,"end":25099594,"strand":1,"description":"small nucleolar RNA, C/D box 116-26 [Source:HGNC Symbol;Acc:HGNC:33092]"}, {"versioned_ensembl_gene_id":"ENSG00000251794.1","gene_symbol":"RNU6-237P","gene_name":"RNA, U6 small nuclear 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:47200]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479672","summary":null,"start":74456541,"end":74456611,"strand":1,"description":"RNA, U6 small nuclear 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:47200]"}, {"versioned_ensembl_gene_id":"ENSG00000284541.1","gene_symbol":"MIR4517","gene_name":"microRNA 4517 [Source:HGNC Symbol;Acc:HGNC:41878]","synonyms":"hsa-mir-4517","biotype":"miRNA","ncbi_id":"100616487","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28958583,"end":28958661,"strand":1,"description":"microRNA 4517 [Source:HGNC Symbol;Acc:HGNC:41878]"}, {"versioned_ensembl_gene_id":"ENSG00000263735.1","gene_symbol":"MIR4662B","gene_name":"microRNA 4662b [Source:HGNC Symbol;Acc:HGNC:41607]","synonyms":"hsa-mir-4662b","biotype":"miRNA","ncbi_id":"100616255","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124821978,"end":124822058,"strand":-1,"description":"microRNA 4662b [Source:HGNC Symbol;Acc:HGNC:41607]"}, {"versioned_ensembl_gene_id":"ENSG00000202341.1","gene_symbol":"RNU6-1051P","gene_name":"RNA, U6 small nuclear 1051, pseudogene [Source:HGNC Symbol;Acc:HGNC:48014]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481932","summary":null,"start":237015204,"end":237015305,"strand":-1,"description":"RNA, U6 small nuclear 1051, pseudogene [Source:HGNC Symbol;Acc:HGNC:48014]"}, {"versioned_ensembl_gene_id":"ENSG00000207639.1","gene_symbol":"MIR193B","gene_name":"microRNA 193b [Source:HGNC Symbol;Acc:HGNC:32087]","synonyms":"MIRN193B,hsa-mir-193b","biotype":"miRNA","ncbi_id":"574455","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14303967,"end":14304049,"strand":1,"description":"microRNA 193b [Source:HGNC Symbol;Acc:HGNC:32087]"}, {"versioned_ensembl_gene_id":"ENSG00000201998.1","gene_symbol":"SNORA23","gene_name":"small nucleolar RNA, H/ACA box 23 [Source:HGNC Symbol;Acc:HGNC:32613]","synonyms":"ACA23","biotype":"snoRNA","ncbi_id":"677808","summary":null,"start":9428773,"end":9428954,"strand":1,"description":"small nucleolar RNA, H/ACA box 23 [Source:HGNC Symbol;Acc:HGNC:32613]"}, {"versioned_ensembl_gene_id":"ENSG00000212017.2","gene_symbol":"MIR548U","gene_name":"microRNA 548u [Source:HGNC Symbol;Acc:HGNC:38316]","synonyms":"hsa-mir-548u","biotype":"miRNA","ncbi_id":"100422884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57390132,"end":57390212,"strand":1,"description":"microRNA 548u [Source:HGNC Symbol;Acc:HGNC:38316]"}, {"versioned_ensembl_gene_id":"ENSG00000252848.1","gene_symbol":"RNA5SP230","gene_name":"RNA, 5S ribosomal pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:43130]","synonyms":"RN5S230","biotype":"rRNA","ncbi_id":"100873488","summary":null,"start":44125752,"end":44125873,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:43130]"}, {"versioned_ensembl_gene_id":"ENSG00000252747.1","gene_symbol":"RNA5SP364","gene_name":"RNA, 5S ribosomal pseudogene 364 [Source:HGNC Symbol;Acc:HGNC:43264]","synonyms":"RN5S364","biotype":"rRNA","ncbi_id":"100873623","summary":null,"start":88051701,"end":88051778,"strand":1,"description":"RNA, 5S ribosomal pseudogene 364 [Source:HGNC Symbol;Acc:HGNC:43264]"}, {"versioned_ensembl_gene_id":"ENSG00000206614.1","gene_symbol":"RNU6-477P","gene_name":"RNA, U6 small nuclear 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:47440]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481330","summary":null,"start":169552449,"end":169552555,"strand":1,"description":"RNA, U6 small nuclear 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:47440]"}, {"versioned_ensembl_gene_id":"ENSG00000199219.1","gene_symbol":"RNU6-500P","gene_name":"RNA, U6 small nuclear 500, pseudogene [Source:HGNC Symbol;Acc:HGNC:47463]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479788","summary":null,"start":173362134,"end":173362240,"strand":-1,"description":"RNA, U6 small nuclear 500, pseudogene [Source:HGNC Symbol;Acc:HGNC:47463]"}, {"versioned_ensembl_gene_id":"ENSG00000199396.1","gene_symbol":"RNA5S5","gene_name":"RNA, 5S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:34366]","synonyms":"RN5S5","biotype":"rRNA","ncbi_id":"100169756","summary":null,"start":228619232,"end":228619350,"strand":-1,"description":"RNA, 5S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:34366]"}, {"versioned_ensembl_gene_id":"ENSG00000265064.1","gene_symbol":"MIR4692","gene_name":"microRNA 4692 [Source:HGNC Symbol;Acc:HGNC:41856]","synonyms":"hsa-mir-4692","biotype":"miRNA","ncbi_id":"100616410","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72783530,"end":72783592,"strand":1,"description":"microRNA 4692 [Source:HGNC Symbol;Acc:HGNC:41856]"}, {"versioned_ensembl_gene_id":"ENSG00000264633.1","gene_symbol":"MIR4271","gene_name":"microRNA 4271 [Source:HGNC Symbol;Acc:HGNC:38332]","synonyms":"hsa-mir-4271","biotype":"miRNA","ncbi_id":"100422952","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49274120,"end":49274186,"strand":1,"description":"microRNA 4271 [Source:HGNC Symbol;Acc:HGNC:38332]"}, {"versioned_ensembl_gene_id":"ENSG00000242065.3","gene_symbol":"RN7SL291P","gene_name":"RNA, 7SL, cytoplasmic 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:46307]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479328","summary":null,"start":44772773,"end":44773061,"strand":-1,"description":"RNA, 7SL, cytoplasmic 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:46307]"}, {"versioned_ensembl_gene_id":"ENSG00000253032.1","gene_symbol":"RNU6-299P","gene_name":"RNA, U6 small nuclear 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:47262]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480389","summary":null,"start":56125671,"end":56125770,"strand":1,"description":"RNA, U6 small nuclear 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:47262]"}, {"versioned_ensembl_gene_id":"ENSG00000221043.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":149695748,"end":149695959,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000274396.1","gene_symbol":"HOTAIRM1_4","gene_name":"HOX antisense intergenic RNA myeloid 1 conserved region 4 [Source:RFAM;Acc:RF01978]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27099856,"end":27099957,"strand":1,"description":"HOX antisense intergenic RNA myeloid 1 conserved region 4 [Source:RFAM;Acc:RF01978]"}, {"versioned_ensembl_gene_id":"ENSG00000207979.1","gene_symbol":"MIR527","gene_name":"microRNA 527 [Source:HGNC Symbol;Acc:HGNC:32129]","synonyms":"MIRN527,hsa-mir-527","biotype":"miRNA","ncbi_id":"574497","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53754018,"end":53754102,"strand":1,"description":"microRNA 527 [Source:HGNC Symbol;Acc:HGNC:32129]"}, {"versioned_ensembl_gene_id":"ENSG00000266564.1","gene_symbol":"MIR4418","gene_name":"microRNA 4418 [Source:HGNC Symbol;Acc:HGNC:41789]","synonyms":"hsa-mir-4418","biotype":"miRNA","ncbi_id":"100616433","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22266239,"end":22266300,"strand":1,"description":"microRNA 4418 [Source:HGNC Symbol;Acc:HGNC:41789]"}, {"versioned_ensembl_gene_id":"ENSG00000283540.1","gene_symbol":"MIR520F","gene_name":"microRNA 520f [Source:HGNC Symbol;Acc:HGNC:32096]","synonyms":"MIRN520F,hsa-mir-520f","biotype":"miRNA","ncbi_id":"574464","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53682159,"end":53682245,"strand":1,"description":"microRNA 520f [Source:HGNC Symbol;Acc:HGNC:32096]"}, {"versioned_ensembl_gene_id":"ENSG00000252635.1","gene_symbol":"RNU2-56P","gene_name":"RNA, U2 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48549]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480221","summary":null,"start":18265690,"end":18265879,"strand":-1,"description":"RNA, U2 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48549]"}, {"versioned_ensembl_gene_id":"ENSG00000200823.1","gene_symbol":"SNORD114-2","gene_name":"small nucleolar RNA, C/D box 114-2 [Source:HGNC Symbol;Acc:HGNC:32990]","synonyms":"14q(II-2)","biotype":"snoRNA","ncbi_id":"767578","summary":null,"start":100951856,"end":100951933,"strand":1,"description":"small nucleolar RNA, C/D box 114-2 [Source:HGNC Symbol;Acc:HGNC:32990]"}, {"versioned_ensembl_gene_id":"ENSG00000212333.1","gene_symbol":"RNA5SP213","gene_name":"RNA, 5S ribosomal pseudogene 213 [Source:HGNC Symbol;Acc:HGNC:43113]","synonyms":"RN5S213","biotype":"rRNA","ncbi_id":"100873473","summary":null,"start":114220681,"end":114220786,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 213 [Source:HGNC Symbol;Acc:HGNC:43113]"}, {"versioned_ensembl_gene_id":"ENSG00000222890.1","gene_symbol":"RNU6-1068P","gene_name":"RNA, U6 small nuclear 1068, pseudogene [Source:HGNC Symbol;Acc:HGNC:48031]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481933","summary":null,"start":101411357,"end":101411459,"strand":1,"description":"RNA, U6 small nuclear 1068, pseudogene [Source:HGNC Symbol;Acc:HGNC:48031]"}, {"versioned_ensembl_gene_id":"ENSG00000202332.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75431990,"end":75432087,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272979.1","gene_symbol":"AC093388.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190454092,"end":190454521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265879.1","gene_symbol":"MIR4748","gene_name":"microRNA 4748 [Source:HGNC Symbol;Acc:HGNC:41557]","synonyms":"hsa-mir-4748","biotype":"miRNA","ncbi_id":"100616425","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10780254,"end":10780335,"strand":1,"description":"microRNA 4748 [Source:HGNC Symbol;Acc:HGNC:41557]"}, {"versioned_ensembl_gene_id":"ENSG00000263849.1","gene_symbol":"MIR4744","gene_name":"microRNA 4744 [Source:HGNC Symbol;Acc:HGNC:41866]","synonyms":"hsa-mir-4744","biotype":"miRNA","ncbi_id":"100616420","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49049687,"end":49049768,"strand":-1,"description":"microRNA 4744 [Source:HGNC Symbol;Acc:HGNC:41866]"}, {"versioned_ensembl_gene_id":"ENSG00000251706.1","gene_symbol":"RNU7-61P","gene_name":"RNA, U7 small nuclear 61 pseudogene [Source:HGNC Symbol;Acc:HGNC:34157]","synonyms":"U7.61","biotype":"snRNA","ncbi_id":"100151656","summary":null,"start":30483135,"end":30483195,"strand":-1,"description":"RNA, U7 small nuclear 61 pseudogene [Source:HGNC Symbol;Acc:HGNC:34157]"}, {"versioned_ensembl_gene_id":"ENSG00000199368.1","gene_symbol":"RNU6-1084P","gene_name":"RNA, U6 small nuclear 1084, pseudogene [Source:HGNC Symbol;Acc:HGNC:48047]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480042","summary":null,"start":11392411,"end":11392517,"strand":-1,"description":"RNA, U6 small nuclear 1084, pseudogene [Source:HGNC Symbol;Acc:HGNC:48047]"}, {"versioned_ensembl_gene_id":"ENSG00000284586.1","gene_symbol":"MIR92B","gene_name":"microRNA 92b [Source:HGNC Symbol;Acc:HGNC:32920]","synonyms":"MIRN92B,hsa-mir-92b","biotype":"miRNA","ncbi_id":"693235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155195177,"end":155195272,"strand":1,"description":"microRNA 92b [Source:HGNC Symbol;Acc:HGNC:32920]"}, {"versioned_ensembl_gene_id":"ENSG00000275257.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28845055,"end":28845291,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284596.1","gene_symbol":"MIR4467","gene_name":"microRNA 4467 [Source:HGNC Symbol;Acc:HGNC:41896]","synonyms":"hsa-mir-4467","biotype":"miRNA","ncbi_id":"100616367","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102471469,"end":102471531,"strand":1,"description":"microRNA 4467 [Source:HGNC Symbol;Acc:HGNC:41896]"}, {"versioned_ensembl_gene_id":"ENSG00000265596.1","gene_symbol":"MIR3659","gene_name":"microRNA 3659 [Source:HGNC Symbol;Acc:HGNC:38882]","synonyms":"hsa-mir-3659","biotype":"miRNA","ncbi_id":"100500801","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38089231,"end":38089329,"strand":1,"description":"microRNA 3659 [Source:HGNC Symbol;Acc:HGNC:38882]"}, {"versioned_ensembl_gene_id":"ENSG00000212302.1","gene_symbol":"SNORD41","gene_name":"Small nucleolar RNA SNORD41 [Source:RFAM;Acc:RF00588]","synonyms":"U41,RNU41","biotype":"snoRNA","ncbi_id":"26810","summary":null,"start":22756761,"end":22756829,"strand":-1,"description":"Small nucleolar RNA SNORD41 [Source:RFAM;Acc:RF00588]"}, {"versioned_ensembl_gene_id":"ENSG00000206875.1","gene_symbol":"RNU6-761P","gene_name":"RNA, U6 small nuclear 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:47724]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480607","summary":null,"start":42018408,"end":42018514,"strand":-1,"description":"RNA, U6 small nuclear 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:47724]"}, {"versioned_ensembl_gene_id":"ENSG00000221400.2","gene_symbol":"SNORD3J","gene_name":"small nucleolar RNA, C/D box 3J [Source:HGNC Symbol;Acc:HGNC:52243]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616985","summary":null,"start":43417249,"end":43417438,"strand":-1,"description":"small nucleolar RNA, C/D box 3J [Source:HGNC Symbol;Acc:HGNC:52243]"}, {"versioned_ensembl_gene_id":"ENSG00000274934.1","gene_symbol":"SMAD5-AS1_4","gene_name":"SMAD5 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02176]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136134082,"end":136134248,"strand":1,"description":"SMAD5 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02176]"}, {"versioned_ensembl_gene_id":"ENSG00000201182.1","gene_symbol":"RNU6-670P","gene_name":"RNA, U6 small nuclear 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:47633]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479863","summary":null,"start":10037552,"end":10037655,"strand":1,"description":"RNA, U6 small nuclear 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:47633]"}, {"versioned_ensembl_gene_id":"ENSG00000202089.1","gene_symbol":"RNU6-1306P","gene_name":"RNA, U6 small nuclear 1306, pseudogene [Source:HGNC Symbol;Acc:HGNC:48269]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480136","summary":null,"start":63882587,"end":63882685,"strand":-1,"description":"RNA, U6 small nuclear 1306, pseudogene [Source:HGNC Symbol;Acc:HGNC:48269]"}, {"versioned_ensembl_gene_id":"ENSG00000222225.1","gene_symbol":"RNU6-447P","gene_name":"RNA, U6 small nuclear 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:47410]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481320","summary":null,"start":152999,"end":153102,"strand":-1,"description":"RNA, U6 small nuclear 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:47410]"}, {"versioned_ensembl_gene_id":"ENSG00000239221.3","gene_symbol":"RN7SL442P","gene_name":"RNA, 7SL, cytoplasmic 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:46458]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481043","summary":null,"start":16191832,"end":16192151,"strand":1,"description":"RNA, 7SL, cytoplasmic 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:46458]"}, {"versioned_ensembl_gene_id":"ENSG00000274514.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12576961,"end":12577237,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252219.2","gene_symbol":"MIR892C","gene_name":"microRNA 892c [Source:HGNC Symbol;Acc:HGNC:50194]","synonyms":"hsa-mir-892c","biotype":"miRNA","ncbi_id":"102466721","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145992750,"end":145992826,"strand":-1,"description":"microRNA 892c [Source:HGNC Symbol;Acc:HGNC:50194]"}, {"versioned_ensembl_gene_id":"ENSG00000241248.3","gene_symbol":"RN7SL727P","gene_name":"RNA, 7SL, cytoplasmic 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:46743]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481121","summary":null,"start":140085855,"end":140086150,"strand":1,"description":"RNA, 7SL, cytoplasmic 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:46743]"}, {"versioned_ensembl_gene_id":"ENSG00000252797.1","gene_symbol":"RN7SKP272","gene_name":"RNA, 7SK small nuclear pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:45996]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479217","summary":null,"start":89987713,"end":89987944,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:45996]"}, {"versioned_ensembl_gene_id":"ENSG00000277411.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":15522195,"end":15522300,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000264136.1","gene_symbol":"MIR3689D2","gene_name":"microRNA 3689d-2 [Source:HGNC Symbol;Acc:HGNC:41846]","synonyms":"hsa-mir-3689d-2","biotype":"miRNA","ncbi_id":"100616344","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850277,"end":134850356,"strand":-1,"description":"microRNA 3689d-2 [Source:HGNC Symbol;Acc:HGNC:41846]"}, {"versioned_ensembl_gene_id":"ENSG00000201255.1","gene_symbol":"RNU6-990P","gene_name":"RNA, U6 small nuclear 990, pseudogene [Source:HGNC Symbol;Acc:HGNC:47953]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480627","summary":null,"start":30360463,"end":30360566,"strand":1,"description":"RNA, U6 small nuclear 990, pseudogene [Source:HGNC Symbol;Acc:HGNC:47953]"}, {"versioned_ensembl_gene_id":"ENSG00000266583.1","gene_symbol":"MIR4478","gene_name":"microRNA 4478 [Source:HGNC Symbol;Acc:HGNC:41759]","synonyms":"hsa-mir-4478","biotype":"miRNA","ncbi_id":"100616312","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122120082,"end":122120167,"strand":-1,"description":"microRNA 4478 [Source:HGNC Symbol;Acc:HGNC:41759]"}, {"versioned_ensembl_gene_id":"ENSG00000202198.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52995620,"end":52995950,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000200656.1","gene_symbol":"SNORA5B","gene_name":"small nucleolar RNA, H/ACA box 5B [Source:HGNC Symbol;Acc:HGNC:32589]","synonyms":"ACA5b","biotype":"snoRNA","ncbi_id":"677795","summary":null,"start":45105968,"end":45106099,"strand":-1,"description":"small nucleolar RNA, H/ACA box 5B [Source:HGNC Symbol;Acc:HGNC:32589]"}, {"versioned_ensembl_gene_id":"ENSG00000263740.2","gene_symbol":"RN7SL4P","gene_name":"RNA, 7SL, cytoplasmic 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10039]","synonyms":"RN7SLP1,RN7SL427P,7L28","biotype":"misc_RNA","ncbi_id":"6030","summary":null,"start":15738515,"end":15738809,"strand":1,"description":"RNA, 7SL, cytoplasmic 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10039]"}, {"versioned_ensembl_gene_id":"ENSG00000200883.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9249649,"end":9249746,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265306.1","gene_symbol":"MIR3195","gene_name":"microRNA 3195 [Source:HGNC Symbol;Acc:HGNC:38250]","synonyms":"hsa-mir-3195","biotype":"miRNA","ncbi_id":"100422838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62064802,"end":62064885,"strand":1,"description":"microRNA 3195 [Source:HGNC Symbol;Acc:HGNC:38250]"}, {"versioned_ensembl_gene_id":"ENSG00000252705.1","gene_symbol":"RNU6-175P","gene_name":"RNA, U6 small nuclear 175, pseudogene [Source:HGNC Symbol;Acc:HGNC:47138]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480558","summary":null,"start":132406752,"end":132406858,"strand":-1,"description":"RNA, U6 small nuclear 175, pseudogene [Source:HGNC Symbol;Acc:HGNC:47138]"}, {"versioned_ensembl_gene_id":"ENSG00000276027.1","gene_symbol":"RNU12","gene_name":"RNA, U12 small nuclear [Source:HGNC Symbol;Acc:HGNC:19380]","synonyms":"RNU12P,RNU12-1","biotype":"snRNA","ncbi_id":"267010","summary":null,"start":42615244,"end":42615393,"strand":1,"description":"RNA, U12 small nuclear [Source:HGNC Symbol;Acc:HGNC:19380]"}, {"versioned_ensembl_gene_id":"ENSG00000201000.1","gene_symbol":"RNA5SP516","gene_name":"RNA, 5S ribosomal pseudogene 516 [Source:HGNC Symbol;Acc:HGNC:43416]","synonyms":"RN5S516","biotype":"rRNA","ncbi_id":"100873567","summary":null,"start":142411053,"end":142411171,"strand":1,"description":"RNA, 5S ribosomal pseudogene 516 [Source:HGNC Symbol;Acc:HGNC:43416]"}, {"versioned_ensembl_gene_id":"ENSG00000200120.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49137762,"end":49137863,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264119.1","gene_symbol":"MIR4795","gene_name":"microRNA 4795 [Source:HGNC Symbol;Acc:HGNC:41757]","synonyms":"hsa-mir-4795","biotype":"miRNA","ncbi_id":"100616161","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87226189,"end":87226277,"strand":-1,"description":"microRNA 4795 [Source:HGNC Symbol;Acc:HGNC:41757]"}, {"versioned_ensembl_gene_id":"ENSG00000222533.1","gene_symbol":"RNU6-705P","gene_name":"RNA, U6 small nuclear 705, pseudogene [Source:HGNC Symbol;Acc:HGNC:47668]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481403","summary":null,"start":181301967,"end":181302070,"strand":1,"description":"RNA, U6 small nuclear 705, pseudogene [Source:HGNC Symbol;Acc:HGNC:47668]"}, {"versioned_ensembl_gene_id":"ENSG00000239007.1","gene_symbol":"RNU7-95P","gene_name":"RNA, U7 small nuclear 95 pseudogene [Source:HGNC Symbol;Acc:HGNC:45629]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479062","summary":null,"start":53688749,"end":53688812,"strand":-1,"description":"RNA, U7 small nuclear 95 pseudogene [Source:HGNC Symbol;Acc:HGNC:45629]"}, {"versioned_ensembl_gene_id":"ENSG00000199327.1","gene_symbol":"RNU6-230P","gene_name":"RNA, U6 small nuclear 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:47193]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479669","summary":null,"start":125119097,"end":125119200,"strand":-1,"description":"RNA, U6 small nuclear 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:47193]"}, {"versioned_ensembl_gene_id":"ENSG00000222148.1","gene_symbol":"RNY4P30","gene_name":"RNA, Ro-associated Y4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42498]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862673","summary":null,"start":49889634,"end":49889728,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42498]"}, {"versioned_ensembl_gene_id":"ENSG00000273519.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54813162,"end":54813268,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000222314.1","gene_symbol":"RNU6-1118P","gene_name":"RNA, U6 small nuclear 1118, pseudogene [Source:HGNC Symbol;Acc:HGNC:48081]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480058","summary":null,"start":38423625,"end":38423728,"strand":1,"description":"RNA, U6 small nuclear 1118, pseudogene [Source:HGNC Symbol;Acc:HGNC:48081]"}, {"versioned_ensembl_gene_id":"ENSG00000284442.1","gene_symbol":"MIR2110","gene_name":"microRNA 2110 [Source:HGNC Symbol;Acc:HGNC:37071]","synonyms":"hsa-mir-2110","biotype":"miRNA","ncbi_id":"100302224","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114174105,"end":114174179,"strand":-1,"description":"microRNA 2110 [Source:HGNC Symbol;Acc:HGNC:37071]"}, {"versioned_ensembl_gene_id":"ENSG00000283497.1","gene_symbol":"MIR3160-2","gene_name":"microRNA 3160-2 [Source:HGNC Symbol;Acc:HGNC:38192]","synonyms":"hsa-mir-3160-2","biotype":"miRNA","ncbi_id":"100422825","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46451807,"end":46451887,"strand":1,"description":"microRNA 3160-2 [Source:HGNC Symbol;Acc:HGNC:38192]"}, {"versioned_ensembl_gene_id":"ENSG00000272232.2","gene_symbol":"RN7SL726P","gene_name":"RNA, 7SL, cytoplasmic 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:46742]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479488","summary":null,"start":70579163,"end":70579461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:46742]"}, {"versioned_ensembl_gene_id":"ENSG00000221031.1","gene_symbol":"CoTC_ribozyme","gene_name":"Beta-globin co-transcriptional cleavage ribozyme [Source:RFAM;Acc:RF00621]","synonyms":null,"biotype":"ribozyme","ncbi_id":null,"summary":null,"start":5224448,"end":5224639,"strand":-1,"description":"Beta-globin co-transcriptional cleavage ribozyme [Source:RFAM;Acc:RF00621]"}, {"versioned_ensembl_gene_id":"ENSG00000251947.1","gene_symbol":"RN7SKP164","gene_name":"RNA, 7SK small nuclear 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{"versioned_ensembl_gene_id":"ENSG00000251891.1","gene_symbol":"RNU7-79P","gene_name":"RNA, U7 small nuclear 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:34175]","synonyms":"U7.79","biotype":"snRNA","ncbi_id":"100151676","summary":null,"start":85389823,"end":85389884,"strand":-1,"description":"RNA, U7 small nuclear 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:34175]"}, {"versioned_ensembl_gene_id":"ENSG00000222412.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31756042,"end":31756136,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207086.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9615267,"end":9615373,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252516.1","gene_symbol":"RNA5SP82","gene_name":"RNA, 5S ribosomal pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:42859]","synonyms":"RN5S82","biotype":"rRNA","ncbi_id":"100873316","summary":null,"start":247204570,"end":247204661,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:42859]"}, {"versioned_ensembl_gene_id":"ENSG00000202430.1","gene_symbol":"RNA5SP88","gene_name":"RNA, 5S ribosomal pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:42886]","synonyms":"RN5S88","biotype":"rRNA","ncbi_id":"100873321","summary":null,"start":24564630,"end":24564738,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:42886]"}, {"versioned_ensembl_gene_id":"ENSG00000240606.3","gene_symbol":"RN7SL564P","gene_name":"RNA, 7SL, cytoplasmic 564, pseudogene [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111771061,"end":111771134,"strand":-1,"description":"microRNA 4771-2 [Source:HGNC Symbol;Acc:HGNC:41774]"}, {"versioned_ensembl_gene_id":"ENSG00000278159.1","gene_symbol":"MIR8062","gene_name":"microRNA 8062 [Source:HGNC Symbol;Acc:HGNC:49975]","synonyms":"hsa-mir-8062","biotype":"miRNA","ncbi_id":"102465865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7371608,"end":7371692,"strand":1,"description":"microRNA 8062 [Source:HGNC Symbol;Acc:HGNC:49975]"}, {"versioned_ensembl_gene_id":"ENSG00000264692.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31392641,"end":31392739,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275726.1","gene_symbol":"MIR6088","gene_name":"microRNA 6088 [Source:HGNC Symbol;Acc:HGNC:50164]","synonyms":"hsa-mir-6088","biotype":"miRNA","ncbi_id":"102464836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45436654,"end":45436704,"strand":1,"description":"microRNA 6088 [Source:HGNC Symbol;Acc:HGNC:50164]"}, {"versioned_ensembl_gene_id":"ENSG00000278598.1","gene_symbol":"MIR6775","gene_name":"microRNA 6775 [Source:HGNC Symbol;Acc:HGNC:50100]","synonyms":"hsa-mir-6775","biotype":"miRNA","ncbi_id":"102465464","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87834592,"end":87834660,"strand":-1,"description":"microRNA 6775 [Source:HGNC Symbol;Acc:HGNC:50100]"}, {"versioned_ensembl_gene_id":"ENSG00000284038.1","gene_symbol":"MIR10A","gene_name":"microRNA 10a [Source:HGNC Symbol;Acc:HGNC:31497]","synonyms":"MIRN10A,hsa-mir-10a","biotype":"miRNA","ncbi_id":"406902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48579838,"end":48579947,"strand":-1,"description":"microRNA 10a [Source:HGNC Symbol;Acc:HGNC:31497]"}, {"versioned_ensembl_gene_id":"ENSG00000266758.1","gene_symbol":"MIR3680-2","gene_name":"microRNA 3680-2 [Source:HGNC Symbol;Acc:HGNC:43472]","synonyms":"hsa-mir-3680-2","biotype":"miRNA","ncbi_id":"100847041","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29599179,"end":29599265,"strand":-1,"description":"microRNA 3680-2 [Source:HGNC Symbol;Acc:HGNC:43472]"}, {"versioned_ensembl_gene_id":"ENSG00000264963.2","gene_symbol":"RN7SL440P","gene_name":"RNA, 7SL, cytoplasmic 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:46456]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481042","summary":null,"start":94150738,"end":94151080,"strand":1,"description":"RNA, 7SL, cytoplasmic 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:46456]"}, {"versioned_ensembl_gene_id":"ENSG00000284644.1","gene_symbol":"AC074386.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144251264,"end":144355707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207269.1","gene_symbol":"RN7SKP62","gene_name":"RNA, 7SK small nuclear pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:45786]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480460","summary":null,"start":100733058,"end":100733386,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:45786]"}, {"versioned_ensembl_gene_id":"ENSG00000283170.1","gene_symbol":"MIR382","gene_name":"microRNA 382 [Source:HGNC Symbol;Acc:HGNC:31875]","synonyms":"MIRN382,hsa-mir-382","biotype":"miRNA","ncbi_id":"494331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101054306,"end":101054381,"strand":1,"description":"microRNA 382 [Source:HGNC Symbol;Acc:HGNC:31875]"}, {"versioned_ensembl_gene_id":"ENSG00000200296.1","gene_symbol":"RNU1-83P","gene_name":"RNA, U1 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:48425]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480176","summary":null,"start":62850738,"end":62850901,"strand":-1,"description":"RNA, U1 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:48425]"}, {"versioned_ensembl_gene_id":"ENSG00000201900.1","gene_symbol":"RNY1P13","gene_name":"RNA, Ro-associated Y1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480310","summary":null,"start":114727720,"end":114727824,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50876]"}, {"versioned_ensembl_gene_id":"ENSG00000206898.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":10296047,"end":10296180,"strand":-1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000263439.1","gene_symbol":"MIR4753","gene_name":"microRNA 4753 [Source:HGNC Symbol;Acc:HGNC:41527]","synonyms":"hsa-mir-4753","biotype":"miRNA","ncbi_id":"100616224","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":235190034,"end":235190116,"strand":-1,"description":"microRNA 4753 [Source:HGNC Symbol;Acc:HGNC:41527]"}, {"versioned_ensembl_gene_id":"ENSG00000284214.1","gene_symbol":"MIR29C","gene_name":"microRNA 29c [Source:HGNC Symbol;Acc:HGNC:31621]","synonyms":"MIRN29C,hsa-mir-29c","biotype":"miRNA","ncbi_id":"407026","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207801852,"end":207801939,"strand":-1,"description":"microRNA 29c [Source:HGNC Symbol;Acc:HGNC:31621]"}, {"versioned_ensembl_gene_id":"ENSG00000252929.1","gene_symbol":"RNU6-218P","gene_name":"RNA, U6 small nuclear 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:47181]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479663","summary":null,"start":6057500,"end":6057604,"strand":1,"description":"RNA, U6 small nuclear 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:47181]"}, {"versioned_ensembl_gene_id":"ENSG00000238949.1","gene_symbol":"RNU7-66P","gene_name":"RNA, U7 small nuclear 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:34162]","synonyms":"U7.66","biotype":"snRNA","ncbi_id":"100151664","summary":null,"start":66728843,"end":66728904,"strand":-1,"description":"RNA, U7 small nuclear 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:34162]"}, {"versioned_ensembl_gene_id":"ENSG00000206924.1","gene_symbol":"RNU6-689P","gene_name":"RNA, U6 small nuclear 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:47652]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479870","summary":null,"start":75020761,"end":75020867,"strand":1,"description":"RNA, U6 small nuclear 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:47652]"}, {"versioned_ensembl_gene_id":"ENSG00000238357.1","gene_symbol":"RNU7-148P","gene_name":"RNA, U7 small nuclear 148 pseudogene [Source:HGNC Symbol;Acc:HGNC:45682]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480823","summary":null,"start":167631480,"end":167631541,"strand":-1,"description":"RNA, U7 small nuclear 148 pseudogene [Source:HGNC Symbol;Acc:HGNC:45682]"}, {"versioned_ensembl_gene_id":"ENSG00000252129.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15574019,"end":15574198,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000266300.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"RNU52,U52,RNU52,U52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31904099,"end":31904165,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000207183.1","gene_symbol":"RNU6-843P","gene_name":"RNA, U6 small nuclear 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:47806]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480614","summary":null,"start":12411398,"end":12411501,"strand":-1,"description":"RNA, U6 small nuclear 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:47806]"}, {"versioned_ensembl_gene_id":"ENSG00000277046.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23170674,"end":23170963,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238730.1","gene_symbol":"RNU7-164P","gene_name":"RNA, U7 small nuclear 164 pseudogene [Source:HGNC Symbol;Acc:HGNC:45698]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479086","summary":null,"start":40535502,"end":40535563,"strand":-1,"description":"RNA, U7 small nuclear 164 pseudogene [Source:HGNC Symbol;Acc:HGNC:45698]"}, {"versioned_ensembl_gene_id":"ENSG00000244197.3","gene_symbol":"RN7SL766P","gene_name":"RNA, 7SL, cytoplasmic 766, pseudogene [Source:HGNC Symbol;Acc:HGNC:46782]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479501","summary":null,"start":21790537,"end":21790845,"strand":1,"description":"RNA, 7SL, cytoplasmic 766, pseudogene [Source:HGNC Symbol;Acc:HGNC:46782]"}, {"versioned_ensembl_gene_id":"ENSG00000200343.1","gene_symbol":"RNA5S8","gene_name":"RNA, 5S ribosomal 8 [Source:HGNC Symbol;Acc:HGNC:34369]","synonyms":"RN5S8","biotype":"rRNA","ncbi_id":"100169759","summary":null,"start":228625909,"end":228626027,"strand":-1,"description":"RNA, 5S ribosomal 8 [Source:HGNC Symbol;Acc:HGNC:34369]"}, {"versioned_ensembl_gene_id":"ENSG00000274012.1","gene_symbol":"RN7SL2","gene_name":"RNA, 7SL, cytoplasmic 2 [Source:HGNC Symbol;Acc:HGNC:23134]","synonyms":"RNSRP2,7SL1c,7L30.1","biotype":"misc_RNA","ncbi_id":"378706","summary":"The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL2, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]","start":49862550,"end":49862849,"strand":-1,"description":"RNA, 7SL, cytoplasmic 2 [Source:HGNC Symbol;Acc:HGNC:23134]"}, {"versioned_ensembl_gene_id":"ENSG00000202239.1","gene_symbol":"RNU6-396P","gene_name":"RNA, U6 small nuclear 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:47359]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481303","summary":null,"start":46525618,"end":46525722,"strand":1,"description":"RNA, U6 small nuclear 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:47359]"}, {"versioned_ensembl_gene_id":"ENSG00000277418.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":48316669,"end":48316770,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000273511.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000201687.1","gene_symbol":"RNU6-1107P","gene_name":"RNA, U6 small nuclear 1107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48070]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481529","summary":null,"start":113859346,"end":113859449,"strand":1,"description":"RNA, U6 small nuclear 1107, pseudogene [Source:HGNC Symbol;Acc:HGNC:48070]"}, {"versioned_ensembl_gene_id":"ENSG00000207134.1","gene_symbol":"RNU6-106P","gene_name":"RNA, U6 small nuclear 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:47069]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479613","summary":null,"start":155358712,"end":155358818,"strand":-1,"description":"RNA, U6 small nuclear 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:47069]"}, {"versioned_ensembl_gene_id":"ENSG00000199711.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99936610,"end":99936711,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207034.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2778941,"end":2779057,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242175.3","gene_symbol":"RN7SL127P","gene_name":"RNA, 7SL, cytoplasmic 127, pseudogene [Source:HGNC Symbol;Acc:HGNC:46143]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480956","summary":null,"start":78898855,"end":78899154,"strand":1,"description":"RNA, 7SL, cytoplasmic 127, pseudogene [Source:HGNC Symbol;Acc:HGNC:46143]"}, {"versioned_ensembl_gene_id":"ENSG00000223282.1","gene_symbol":"RN7SKP165","gene_name":"RNA, 7SK small nuclear pseudogene 165 [Source:HGNC Symbol;Acc:HGNC:45889]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480367","summary":null,"start":226445937,"end":226446292,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 165 [Source:HGNC Symbol;Acc:HGNC:45889]"}, {"versioned_ensembl_gene_id":"ENSG00000252178.1","gene_symbol":"RNU7-69P","gene_name":"RNA, U7 small nuclear 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:34165]","synonyms":"U7.69","biotype":"snRNA","ncbi_id":"100151666","summary":null,"start":123772078,"end":123772139,"strand":-1,"description":"RNA, U7 small nuclear 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:34165]"}, {"versioned_ensembl_gene_id":"ENSG00000201602.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":248594925,"end":248595033,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238423.1","gene_symbol":"SNORD42B","gene_name":"small nucleolar RNA, C/D box 42B [Source:HGNC Symbol;Acc:HGNC:10181]","synonyms":"U42B,RNU42B","biotype":"snoRNA","ncbi_id":"26808","summary":null,"start":28720550,"end":28720616,"strand":1,"description":"small nucleolar RNA, C/D box 42B [Source:HGNC Symbol;Acc:HGNC:10181]"}, {"versioned_ensembl_gene_id":"ENSG00000280632.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133302618,"end":133302711,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207251.1","gene_symbol":"RNU6-342P","gene_name":"RNA, U6 small nuclear 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:47305]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479718","summary":null,"start":27265580,"end":27265683,"strand":-1,"description":"RNA, U6 small nuclear 342, 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{"versioned_ensembl_gene_id":"ENSG00000251811.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43472477,"end":43472596,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212257.1","gene_symbol":"RNU6-1176P","gene_name":"RNA, U6 small nuclear 1176, pseudogene [Source:HGNC Symbol;Acc:HGNC:48139]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481551","summary":null,"start":65022968,"end":65023074,"strand":-1,"description":"RNA, U6 small nuclear 1176, pseudogene [Source:HGNC Symbol;Acc:HGNC:48139]"}, {"versioned_ensembl_gene_id":"ENSG00000206982.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128584390,"end":128584491,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276565.1","gene_symbol":"AP006285.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1586202,"end":1591699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252717.1","gene_symbol":"RNU6-352P","gene_name":"RNA, U6 small nuclear 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:47315]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480573","summary":null,"start":101859851,"end":101859957,"strand":1,"description":"RNA, U6 small nuclear 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:47315]"}, {"versioned_ensembl_gene_id":"ENSG00000199515.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41065554,"end":41065646,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199556.1","gene_symbol":"RNA5SP361","gene_name":"RNA, 5S ribosomal pseudogene 361 [Source:HGNC Symbol;Acc:HGNC:43261]","synonyms":"RN5S361","biotype":"rRNA","ncbi_id":"100873620","summary":null,"start":45117771,"end":45117888,"strand":1,"description":"RNA, 5S ribosomal pseudogene 361 [Source:HGNC Symbol;Acc:HGNC:43261]"}, {"versioned_ensembl_gene_id":"ENSG00000207100.1","gene_symbol":"SNORA8","gene_name":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]","synonyms":"ACA8","biotype":"snoRNA","ncbi_id":"654320","summary":null,"start":133152754,"end":133152892,"strand":1,"description":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]"}, {"versioned_ensembl_gene_id":"ENSG00000206700.1","gene_symbol":"RNU6-723P","gene_name":"RNA, U6 small nuclear 723, pseudogene [Source:HGNC Symbol;Acc:HGNC:47686]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479886","summary":null,"start":48344209,"end":48344315,"strand":1,"description":"RNA, U6 small nuclear 723, pseudogene [Source:HGNC Symbol;Acc:HGNC:47686]"}, {"versioned_ensembl_gene_id":"ENSG00000252386.1","gene_symbol":"RNU6-1018P","gene_name":"RNA, U6 small nuclear 1018, pseudogene [Source:HGNC Symbol;Acc:HGNC:47981]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481502","summary":null,"start":41684986,"end":41685091,"strand":-1,"description":"RNA, U6 small nuclear 1018, pseudogene [Source:HGNC Symbol;Acc:HGNC:47981]"}, {"versioned_ensembl_gene_id":"ENSG00000275776.1","gene_symbol":"RN7SL185P","gene_name":"RNA, 7SL, cytoplasmic 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:46201]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479289","summary":null,"start":32394365,"end":32394613,"strand":-1,"description":"RNA, 7SL, cytoplasmic 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:46201]"}, {"versioned_ensembl_gene_id":"ENSG00000201925.1","gene_symbol":"RNA5S15","gene_name":"RNA, 5S ribosomal 15 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207136.1","gene_symbol":"RNU6-769P","gene_name":"RNA, U6 small nuclear 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:47732]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479906","summary":null,"start":50633273,"end":50633376,"strand":1,"description":"RNA, U6 small nuclear 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:47732]"}, {"versioned_ensembl_gene_id":"ENSG00000275823.1","gene_symbol":"DLEU2_3","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63549294,"end":63549366,"strand":-1,"description":"Deleted in lymphocytic leukemia 2 conserved region 3 [Source:RFAM;Acc:RF02107]"}, {"versioned_ensembl_gene_id":"ENSG00000240647.3","gene_symbol":"RN7SL305P","gene_name":"RNA, 7SL, cytoplasmic 305, pseudogene [Source:HGNC 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[Source:HGNC Symbol;Acc:HGNC:46928]"}, {"versioned_ensembl_gene_id":"ENSG00000199490.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49920597,"end":49920694,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223238.1","gene_symbol":"RNA5SP294","gene_name":"RNA, 5S ribosomal pseudogene 294 [Source:HGNC Symbol;Acc:HGNC:43194]","synonyms":"RN5S294","biotype":"rRNA","ncbi_id":"100873547","summary":null,"start":111411644,"end":111411742,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 294 [Source:HGNC Symbol;Acc:HGNC:43194]"}, {"versioned_ensembl_gene_id":"ENSG00000206728.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23273807,"end":23273910,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263723.1","gene_symbol":"SNORD39","gene_name":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":237869904,"end":237869982,"strand":1,"description":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]"}, {"versioned_ensembl_gene_id":"ENSG00000276516.1","gene_symbol":"RN7SL284P","gene_name":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480999","summary":null,"start":77912271,"end":77912545,"strand":-1,"description":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]"}, {"versioned_ensembl_gene_id":"ENSG00000252047.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":103434994,"end":103435092,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239367.2","gene_symbol":"RN7SL477P","gene_name":"RNA, 7SL, cytoplasmic 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:46493]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479397","summary":null,"start":1570575,"end":1570860,"strand":-1,"description":"RNA, 7SL, cytoplasmic 477, pseudogene [Source:HGNC Symbol;Acc:HGNC:46493]"}, {"versioned_ensembl_gene_id":"ENSG00000222546.1","gene_symbol":"RNA5SP251","gene_name":"RNA, 5S ribosomal pseudogene 251 [Source:HGNC Symbol;Acc:HGNC:43151]","synonyms":"RN5S251","biotype":"rRNA","ncbi_id":"100873507","summary":null,"start":3700492,"end":3700628,"strand":1,"description":"RNA, 5S ribosomal pseudogene 251 [Source:HGNC Symbol;Acc:HGNC:43151]"}, {"versioned_ensembl_gene_id":"ENSG00000283188.1","gene_symbol":"MIR2052","gene_name":"microRNA 2052 [Source:HGNC Symbol;Acc:HGNC:37068]","synonyms":"hsa-mir-2052","biotype":"miRNA","ncbi_id":"100302260","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74705693,"end":74705747,"strand":1,"description":"microRNA 2052 [Source:HGNC Symbol;Acc:HGNC:37068]"}, {"versioned_ensembl_gene_id":"ENSG00000207081.1","gene_symbol":"RNU6-616P","gene_name":"RNA, U6 small nuclear 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:47579]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479838","summary":null,"start":134918310,"end":134918416,"strand":-1,"description":"RNA, U6 small nuclear 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:47579]"}, {"versioned_ensembl_gene_id":"ENSG00000272015.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"E2-1,RNU108,E2,RNE2","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":38894785,"end":38894867,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000227482.1","gene_symbol":"AL157702.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113650956,"end":113682855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263649.1","gene_symbol":"MIR3135B","gene_name":"microRNA 3135b [Source:HGNC Symbol;Acc:HGNC:41783]","synonyms":"hsa-mir-3135b","biotype":"miRNA","ncbi_id":"100616218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32749912,"end":32749979,"strand":-1,"description":"microRNA 3135b [Source:HGNC Symbol;Acc:HGNC:41783]"}, {"versioned_ensembl_gene_id":"ENSG00000240877.3","gene_symbol":"RN7SL521P","gene_name":"RNA, 7SL, cytoplasmic 521, pseudogene [Source:HGNC Symbol;Acc:HGNC:46537]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479413","summary":null,"start":149125690,"end":149125986,"strand":-1,"description":"RNA, 7SL, cytoplasmic 521, pseudogene [Source:HGNC Symbol;Acc:HGNC:46537]"}, {"versioned_ensembl_gene_id":"ENSG00000207049.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":236153071,"end":236153172,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284286.1","gene_symbol":"MIR718","gene_name":"microRNA 718 [Source:HGNC Symbol;Acc:HGNC:37317]","synonyms":"hsa-mir-718","biotype":"miRNA","ncbi_id":"100313781","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154019920,"end":154019989,"strand":-1,"description":"microRNA 718 [Source:HGNC Symbol;Acc:HGNC:37317]"}, {"versioned_ensembl_gene_id":"ENSG00000202354.1","gene_symbol":"RNY3","gene_name":"RNA, Ro-associated Y3 [Source:HGNC Symbol;Acc:HGNC:10243]","synonyms":"hY3","biotype":"misc_RNA","ncbi_id":"6085","summary":null,"start":148983755,"end":148983856,"strand":1,"description":"RNA, Ro-associated Y3 [Source:HGNC Symbol;Acc:HGNC:10243]"}, {"versioned_ensembl_gene_id":"ENSG00000208018.1","gene_symbol":"MIR645","gene_name":"microRNA 645 [Source:HGNC Symbol;Acc:HGNC:32901]","synonyms":"MIRN645,hsa-mir-645","biotype":"miRNA","ncbi_id":"693230","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50585786,"end":50585879,"strand":1,"description":"microRNA 645 [Source:HGNC Symbol;Acc:HGNC:32901]"}, {"versioned_ensembl_gene_id":"ENSG00000263403.1","gene_symbol":"MIR4673","gene_name":"microRNA 4673 [Source:HGNC Symbol;Acc:HGNC:41574]","synonyms":"hsa-mir-4673","biotype":"miRNA","ncbi_id":"100616242","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136519568,"end":136519626,"strand":-1,"description":"microRNA 4673 [Source:HGNC Symbol;Acc:HGNC:41574]"}, {"versioned_ensembl_gene_id":"ENSG00000283734.1","gene_symbol":"MIR4785","gene_name":"microRNA 4785 [Source:HGNC Symbol;Acc:HGNC:41889]","synonyms":"hsa-mir-4785","biotype":"miRNA","ncbi_id":"100616364","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160407810,"end":160407882,"strand":-1,"description":"microRNA 4785 [Source:HGNC Symbol;Acc:HGNC:41889]"}, {"versioned_ensembl_gene_id":"ENSG00000269782.1","gene_symbol":"MIR1470","gene_name":"microRNA 1470 [Source:HGNC Symbol;Acc:HGNC:35379]","synonyms":"MIRN1470,hsa-mir-1470","biotype":"miRNA","ncbi_id":"100302127","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15449548,"end":15449608,"strand":1,"description":"microRNA 1470 [Source:HGNC Symbol;Acc:HGNC:35379]"}, {"versioned_ensembl_gene_id":"ENSG00000252927.1","gene_symbol":"RNA5SP404","gene_name":"RNA, 5S ribosomal pseudogene 404 [Source:HGNC Symbol;Acc:HGNC:43304]","synonyms":"RN5S404","biotype":"rRNA","ncbi_id":"100873656","summary":null,"start":9600097,"end":9600228,"strand":1,"description":"RNA, 5S ribosomal pseudogene 404 [Source:HGNC Symbol;Acc:HGNC:43304]"}, {"versioned_ensembl_gene_id":"ENSG00000251352.1","gene_symbol":"AC122714.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180671892,"end":180672598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278412.1","gene_symbol":"MIR6854","gene_name":"microRNA 6854 [Source:HGNC Symbol;Acc:HGNC:50084]","synonyms":"hsa-mir-6854","biotype":"miRNA","ncbi_id":"102465514","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98229149,"end":98229217,"strand":-1,"description":"microRNA 6854 [Source:HGNC Symbol;Acc:HGNC:50084]"}, {"versioned_ensembl_gene_id":"ENSG00000266530.1","gene_symbol":"MIR4318","gene_name":"microRNA 4318 [Source:HGNC Symbol;Acc:HGNC:38333]","synonyms":"hsa-mir-4318","biotype":"miRNA","ncbi_id":"100422857","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37657135,"end":37657215,"strand":1,"description":"microRNA 4318 [Source:HGNC Symbol;Acc:HGNC:38333]"}, {"versioned_ensembl_gene_id":"ENSG00000251745.1","gene_symbol":"RNU7-124P","gene_name":"RNA, U7 small nuclear 124 pseudogene [Source:HGNC Symbol;Acc:HGNC:45658]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479072","summary":null,"start":37936707,"end":37936768,"strand":-1,"description":"RNA, U7 small nuclear 124 pseudogene [Source:HGNC Symbol;Acc:HGNC:45658]"}, {"versioned_ensembl_gene_id":"ENSG00000266324.1","gene_symbol":"MIR4663","gene_name":"microRNA 4663 [Source:HGNC Symbol;Acc:HGNC:41623]","synonyms":"hsa-mir-4663","biotype":"miRNA","ncbi_id":"100616260","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123215788,"end":123215863,"strand":-1,"description":"microRNA 4663 [Source:HGNC Symbol;Acc:HGNC:41623]"}, {"versioned_ensembl_gene_id":"ENSG00000207351.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":184086791,"end":184086903,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276326.1","gene_symbol":"MIR2909","gene_name":"microRNA 2909 [Source:HGNC Symbol;Acc:HGNC:38372]","synonyms":"hsa-mir-2909","biotype":"miRNA","ncbi_id":"100422969","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37033745,"end":37033813,"strand":1,"description":"microRNA 2909 [Source:HGNC Symbol;Acc:HGNC:38372]"}, {"versioned_ensembl_gene_id":"ENSG00000265375.1","gene_symbol":"MIR4679-2","gene_name":"microRNA 4679-2 [Source:HGNC Symbol;Acc:HGNC:41890]","synonyms":"hsa-mir-4679-2","biotype":"miRNA","ncbi_id":"100616192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89063335,"end":89063411,"strand":-1,"description":"microRNA 4679-2 [Source:HGNC Symbol;Acc:HGNC:41890]"}, {"versioned_ensembl_gene_id":"ENSG00000208037.1","gene_symbol":"MIR320A","gene_name":"microRNA 320a [Source:HGNC Symbol;Acc:HGNC:31632]","synonyms":"hsa-mir-320,MIRN320A,MIRN320","biotype":"miRNA","ncbi_id":"407037","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22244962,"end":22245043,"strand":-1,"description":"microRNA 320a [Source:HGNC Symbol;Acc:HGNC:31632]"}, {"versioned_ensembl_gene_id":"ENSG00000277617.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32269338,"end":32269597,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212595.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":151026295,"end":151026406,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000199220.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":114657949,"end":114658062,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263894.1","gene_symbol":"MIR3925","gene_name":"microRNA 3925 [Source:HGNC Symbol;Acc:HGNC:38996]","synonyms":"hsa-mir-3925","biotype":"miRNA","ncbi_id":"100500885","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36622436,"end":36622512,"strand":-1,"description":"microRNA 3925 [Source:HGNC Symbol;Acc:HGNC:38996]"}, {"versioned_ensembl_gene_id":"ENSG00000239250.3","gene_symbol":"RN7SL271P","gene_name":"RNA, 7SL, cytoplasmic 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:46287]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479321","summary":null,"start":71827177,"end":71827471,"strand":1,"description":"RNA, 7SL, cytoplasmic 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:46287]"}, {"versioned_ensembl_gene_id":"ENSG00000252252.1","gene_symbol":"RNU6-687P","gene_name":"RNA, U6 small nuclear 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:47650]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479869","summary":null,"start":54452423,"end":54452511,"strand":-1,"description":"RNA, U6 small nuclear 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:47650]"}, {"versioned_ensembl_gene_id":"ENSG00000278401.1","gene_symbol":"AP000351.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24022930,"end":24023387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200875.1","gene_symbol":"RNU6-340P","gene_name":"RNA, U6 small nuclear 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:47303]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479717","summary":null,"start":2649761,"end":2649867,"strand":-1,"description":"RNA, U6 small nuclear 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:47303]"}, {"versioned_ensembl_gene_id":"ENSG00000266478.1","gene_symbol":"MIR5197","gene_name":"microRNA 5197 [Source:HGNC Symbol;Acc:HGNC:43450]","synonyms":"hsa-mir-5197","biotype":"miRNA","ncbi_id":"100846991","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143679860,"end":143679971,"strand":1,"description":"microRNA 5197 [Source:HGNC Symbol;Acc:HGNC:43450]"}, {"versioned_ensembl_gene_id":"ENSG00000278774.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43273101,"end":43273292,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000207956.1","gene_symbol":"MIR579","gene_name":"microRNA 579 [Source:HGNC Symbol;Acc:HGNC:32835]","synonyms":"MIRN579,hsa-mir-579","biotype":"miRNA","ncbi_id":"693164","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32394378,"end":32394475,"strand":-1,"description":"microRNA 579 [Source:HGNC Symbol;Acc:HGNC:32835]"}, {"versioned_ensembl_gene_id":"ENSG00000252230.1","gene_symbol":"SNORD111","gene_name":"Small nucleolar RNA SNORD111 [Source:RFAM;Acc:RF00611]","synonyms":"HBII-82","biotype":"snoRNA","ncbi_id":"692214","summary":null,"start":34637696,"end":34637781,"strand":-1,"description":"Small nucleolar RNA SNORD111 [Source:RFAM;Acc:RF00611]"}, {"versioned_ensembl_gene_id":"ENSG00000251900.1","gene_symbol":"VTRNA2-2P","gene_name":"vault RNA 2-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46889]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479538","summary":null,"start":65555432,"end":65555534,"strand":-1,"description":"vault RNA 2-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46889]"}, {"versioned_ensembl_gene_id":"ENSG00000277209.1","gene_symbol":"RPPH1","gene_name":"ribonuclease P RNA component H1 [Source:HGNC Symbol;Acc:HGNC:19273]","synonyms":"RPPH1-1,H1RNA","biotype":"ribozyme","ncbi_id":"85495","summary":"H1RNA is the RNA component of the RNase P ribonucleoprotein, an endoribonuclease that cleaves tRNA precursor molecules to form the mature 5-prime termini of their tRNA sequences (Baer et al., 1989 [PubMed 2308839]).[supplied by OMIM, Mar 2008]","start":20343075,"end":20343407,"strand":-1,"description":"ribonuclease P RNA component H1 [Source:HGNC Symbol;Acc:HGNC:19273]"}, {"versioned_ensembl_gene_id":"ENSG00000283990.1","gene_symbol":"MIRLET7A3","gene_name":"microRNA let-7a-3 [Source:HGNC Symbol;Acc:HGNC:31478]","synonyms":"MIRNLET7A3,hsa-let-7a-3","biotype":"miRNA","ncbi_id":"406883","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46112749,"end":46112822,"strand":1,"description":"microRNA let-7a-3 [Source:HGNC Symbol;Acc:HGNC:31478]"}, {"versioned_ensembl_gene_id":"ENSG00000251940.1","gene_symbol":"SNORA15","gene_name":"Small nucleolar RNA SNORA15 [Source:RFAM;Acc:RF00398]","synonyms":"SNORA15A,ACA15","biotype":"snoRNA","ncbi_id":"677803","summary":null,"start":19249873,"end":19249966,"strand":1,"description":"Small nucleolar RNA SNORA15 [Source:RFAM;Acc:RF00398]"}, {"versioned_ensembl_gene_id":"ENSG00000266317.2","gene_symbol":"RN7SL703P","gene_name":"RNA, 7SL, cytoplasmic 703, pseudogene [Source:HGNC Symbol;Acc:HGNC:46719]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479479","summary":null,"start":181813401,"end":181813702,"strand":1,"description":"RNA, 7SL, cytoplasmic 703, pseudogene [Source:HGNC Symbol;Acc:HGNC:46719]"}, {"versioned_ensembl_gene_id":"ENSG00000207328.1","gene_symbol":"RNU6-636P","gene_name":"RNA, U6 small nuclear 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:47599]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480597","summary":null,"start":37203610,"end":37203716,"strand":1,"description":"RNA, U6 small nuclear 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:47599]"}, {"versioned_ensembl_gene_id":"ENSG00000200563.1","gene_symbol":"RNU6-640P","gene_name":"RNA, U6 small nuclear 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:47603]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479850","summary":null,"start":86515204,"end":86515308,"strand":-1,"description":"RNA, U6 small nuclear 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:47603]"}, {"versioned_ensembl_gene_id":"ENSG00000239096.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":179614775,"end":179614878,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000202056.1","gene_symbol":"RNA5SP19","gene_name":"RNA, 5S ribosomal pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42587]","synonyms":"RN5S19","biotype":"rRNA","ncbi_id":"100873274","summary":null,"start":228555793,"end":228555901,"strand":1,"description":"RNA, 5S ribosomal pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42587]"}, {"versioned_ensembl_gene_id":"ENSG00000265007.1","gene_symbol":"MIR4327","gene_name":"microRNA 4327 [Source:HGNC Symbol;Acc:HGNC:38355]","synonyms":"hsa-mir-4327","biotype":"miRNA","ncbi_id":"100422891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30375294,"end":30375378,"strand":-1,"description":"microRNA 4327 [Source:HGNC Symbol;Acc:HGNC:38355]"}, {"versioned_ensembl_gene_id":"ENSG00000241997.3","gene_symbol":"RN7SL323P","gene_name":"RNA, 7SL, cytoplasmic 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:46339]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479341","summary":null,"start":56022019,"end":56022313,"strand":-1,"description":"RNA, 7SL, cytoplasmic 323, pseudogene [Source:HGNC Symbol;Acc:HGNC:46339]"}, {"versioned_ensembl_gene_id":"ENSG00000275108.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":98987387,"end":98987449,"strand":1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000212517.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":5121417,"end":5121539,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000284125.1","gene_symbol":"MIR1825","gene_name":"microRNA 1825 [Source:HGNC Symbol;Acc:HGNC:35389]","synonyms":"MIRN1825,hsa-mir-1825","biotype":"miRNA","ncbi_id":"100302183","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32237795,"end":32237847,"strand":1,"description":"microRNA 1825 [Source:HGNC Symbol;Acc:HGNC:35389]"}, {"versioned_ensembl_gene_id":"ENSG00000265093.2","gene_symbol":"RN7SL246P","gene_name":"RNA, 7SL, cytoplasmic 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:46262]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480989","summary":null,"start":45874035,"end":45874330,"strand":1,"description":"RNA, 7SL, cytoplasmic 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:46262]"}, {"versioned_ensembl_gene_id":"ENSG00000283222.1","gene_symbol":"MIR4433A","gene_name":"microRNA 4433a [Source:HGNC Symbol;Acc:HGNC:41634]","synonyms":"MIR4433,hsa-mir-4433","biotype":"miRNA","ncbi_id":"100616265","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64340759,"end":64340839,"strand":1,"description":"microRNA 4433a [Source:HGNC Symbol;Acc:HGNC:41634]"}, {"versioned_ensembl_gene_id":"ENSG00000201013.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":233379843,"end":233379955,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283978.1","gene_symbol":"MIR365B","gene_name":"microRNA 365b [Source:HGNC Symbol;Acc:HGNC:33693]","synonyms":"MIRN365-2,MIR365-2,hsa-mir-365-2","biotype":"miRNA","ncbi_id":"100126356","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31575411,"end":31575521,"strand":1,"description":"microRNA 365b [Source:HGNC Symbol;Acc:HGNC:33693]"}, {"versioned_ensembl_gene_id":"ENSG00000202313.1","gene_symbol":"RNU1-64P","gene_name":"RNA, U1 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48406]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480168","summary":null,"start":11503509,"end":11503671,"strand":-1,"description":"RNA, U1 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48406]"}, {"versioned_ensembl_gene_id":"ENSG00000239080.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":136134317,"end":136134420,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000200208.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23457584,"end":23457685,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274300.1","gene_symbol":"MIR6864","gene_name":"microRNA 6864 [Source:HGNC Symbol;Acc:HGNC:50226]","synonyms":"hsa-mir-6864","biotype":"miRNA","ncbi_id":"102465521","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4969702,"end":4969771,"strand":-1,"description":"microRNA 6864 [Source:HGNC Symbol;Acc:HGNC:50226]"}, {"versioned_ensembl_gene_id":"ENSG00000207419.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"RNU67,U67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":11709819,"end":11709960,"strand":1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000199200.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34201979,"end":34202074,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278523.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61928634,"end":61928704,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266643.1","gene_symbol":"MIR3677","gene_name":"microRNA 3677 [Source:HGNC Symbol;Acc:HGNC:38932]","synonyms":"hsa-mir-3677","biotype":"miRNA","ncbi_id":"100500812","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2270713,"end":2270772,"strand":1,"description":"microRNA 3677 [Source:HGNC Symbol;Acc:HGNC:38932]"}, {"versioned_ensembl_gene_id":"ENSG00000239030.1","gene_symbol":"RNU6-956P","gene_name":"RNA, U6 small nuclear 956, pseudogene [Source:HGNC Symbol;Acc:HGNC:47919]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480404","summary":null,"start":94712409,"end":94712511,"strand":1,"description":"RNA, U6 small nuclear 956, pseudogene [Source:HGNC Symbol;Acc:HGNC:47919]"}, {"versioned_ensembl_gene_id":"ENSG00000268154.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":154950210,"end":154950492,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000198984.1","gene_symbol":"MIR345","gene_name":"microRNA 345 [Source:HGNC Symbol;Acc:HGNC:31779]","synonyms":"MIRN345,hsa-mir-345","biotype":"miRNA","ncbi_id":"442910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100307859,"end":100307956,"strand":1,"description":"microRNA 345 [Source:HGNC Symbol;Acc:HGNC:31779]"}, {"versioned_ensembl_gene_id":"ENSG00000222987.1","gene_symbol":"RN7SKP68","gene_name":"RNA, 7SK small nuclear pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:45792]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480854","summary":null,"start":102302504,"end":102302810,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:45792]"}, {"versioned_ensembl_gene_id":"ENSG00000266531.1","gene_symbol":"MIR4706","gene_name":"microRNA 4706 [Source:HGNC Symbol;Acc:HGNC:41576]","synonyms":"hsa-mir-4706","biotype":"miRNA","ncbi_id":"100616490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65044688,"end":65044769,"strand":1,"description":"microRNA 4706 [Source:HGNC Symbol;Acc:HGNC:41576]"}, {"versioned_ensembl_gene_id":"ENSG00000272393.1","gene_symbol":"RNU6-92P","gene_name":"RNA, U6 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:47055]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479607","summary":null,"start":133082829,"end":133082932,"strand":1,"description":"RNA, U6 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:47055]"}, {"versioned_ensembl_gene_id":"ENSG00000201451.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133337728,"end":133337824,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277488.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":37940704,"end":37940790,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000276528.1","gene_symbol":"HOTAIRM1_1","gene_name":"HOX antisense intergenic RNA myeloid 1 conserved region 1 [Source:RFAM;Acc:RF01975]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27096124,"end":27096248,"strand":1,"description":"HOX antisense intergenic RNA myeloid 1 conserved region 1 [Source:RFAM;Acc:RF01975]"}, {"versioned_ensembl_gene_id":"ENSG00000274824.1","gene_symbol":"MIR7152","gene_name":"microRNA 7152 [Source:HGNC Symbol;Acc:HGNC:50257]","synonyms":"hsa-mir-7152","biotype":"miRNA","ncbi_id":"102465689","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71790747,"end":71790800,"strand":1,"description":"microRNA 7152 [Source:HGNC Symbol;Acc:HGNC:50257]"}, {"versioned_ensembl_gene_id":"ENSG00000200424.1","gene_symbol":"RNU6-1155P","gene_name":"RNA, U6 small nuclear 1155, pseudogene [Source:HGNC Symbol;Acc:HGNC:48118]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481544","summary":null,"start":58744251,"end":58744357,"strand":-1,"description":"RNA, U6 small nuclear 1155, pseudogene [Source:HGNC Symbol;Acc:HGNC:48118]"}, {"versioned_ensembl_gene_id":"ENSG00000240936.3","gene_symbol":"RN7SL554P","gene_name":"RNA, 7SL, cytoplasmic 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:46570]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479423","summary":null,"start":6938606,"end":6938897,"strand":-1,"description":"RNA, 7SL, cytoplasmic 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:46570]"}, {"versioned_ensembl_gene_id":"ENSG00000206726.1","gene_symbol":"RNU6-259P","gene_name":"RNA, U6 small nuclear 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:47222]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481260","summary":null,"start":124989219,"end":124989325,"strand":1,"description":"RNA, U6 small nuclear 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:47222]"}, {"versioned_ensembl_gene_id":"ENSG00000252580.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":26796173,"end":26796304,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000252337.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":106546665,"end":106546803,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000223026.1","gene_symbol":"RN7SKP247","gene_name":"RNA, 7SK small nuclear pseudogene 247 [Source:HGNC Symbol;Acc:HGNC:45971]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479205","summary":null,"start":81251789,"end":81252096,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 247 [Source:HGNC Symbol;Acc:HGNC:45971]"}, {"versioned_ensembl_gene_id":"ENSG00000200579.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38014568,"end":38014669,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200974.1","gene_symbol":"RNU4-87P","gene_name":"RNA, U4 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:47023]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479598","summary":null,"start":165252580,"end":165252661,"strand":1,"description":"RNA, U4 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:47023]"}, {"versioned_ensembl_gene_id":"ENSG00000264470.1","gene_symbol":"MIR4794","gene_name":"microRNA 4794 [Source:HGNC Symbol;Acc:HGNC:41829]","synonyms":"hsa-mir-4794","biotype":"miRNA","ncbi_id":"100616338","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64579847,"end":64579923,"strand":1,"description":"microRNA 4794 [Source:HGNC Symbol;Acc:HGNC:41829]"}, {"versioned_ensembl_gene_id":"ENSG00000212521.1","gene_symbol":"RNU6-918P","gene_name":"RNA, U6 small nuclear 918, pseudogene [Source:HGNC Symbol;Acc:HGNC:47881]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481469","summary":null,"start":98032230,"end":98032335,"strand":1,"description":"RNA, U6 small nuclear 918, pseudogene [Source:HGNC Symbol;Acc:HGNC:47881]"}, {"versioned_ensembl_gene_id":"ENSG00000241588.3","gene_symbol":"RN7SL484P","gene_name":"RNA, 7SL, cytoplasmic 484, pseudogene [Source:HGNC Symbol;Acc:HGNC:46500]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479400","summary":null,"start":99791209,"end":99791410,"strand":1,"description":"RNA, 7SL, cytoplasmic 484, pseudogene [Source:HGNC Symbol;Acc:HGNC:46500]"}, {"versioned_ensembl_gene_id":"ENSG00000264036.2","gene_symbol":"RN7SL198P","gene_name":"RNA, 7SL, cytoplasmic 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:46214]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479294","summary":null,"start":12328132,"end":12328389,"strand":-1,"description":"RNA, 7SL, cytoplasmic 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:46214]"}, {"versioned_ensembl_gene_id":"ENSG00000274836.1","gene_symbol":"SMCR2_2","gene_name":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 2 [Source:RFAM;Acc:RF02178]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17676211,"end":17676371,"strand":1,"description":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 2 [Source:RFAM;Acc:RF02178]"}, {"versioned_ensembl_gene_id":"ENSG00000279336.1","gene_symbol":"AL353662.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":34201273,"end":34201515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222952.1","gene_symbol":"RNA5SP41","gene_name":"RNA, 5S ribosomal pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:42817]","synonyms":"RN5S41","biotype":"rRNA","ncbi_id":"100873280","summary":null,"start":13623184,"end":13623284,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:42817]"}, {"versioned_ensembl_gene_id":"ENSG00000266295.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31526642,"end":31526717,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000199094.3","gene_symbol":"MIR30C2","gene_name":"microRNA 30c-2 [Source:HGNC Symbol;Acc:HGNC:31627]","synonyms":"MIRN30C2,hsa-mir-30c-2","biotype":"miRNA","ncbi_id":"407032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71376960,"end":71377031,"strand":-1,"description":"microRNA 30c-2 [Source:HGNC Symbol;Acc:HGNC:31627]"}, {"versioned_ensembl_gene_id":"ENSG00000276770.1","gene_symbol":"MIR6780B","gene_name":"microRNA 6780b [Source:HGNC Symbol;Acc:HGNC:50237]","synonyms":"hsa-mir-6780b","biotype":"miRNA","ncbi_id":"102466746","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43434542,"end":43434620,"strand":1,"description":"microRNA 6780b [Source:HGNC Symbol;Acc:HGNC:50237]"}, {"versioned_ensembl_gene_id":"ENSG00000201665.1","gene_symbol":"RN7SKP6","gene_name":"RNA, 7SK small nuclear pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42624]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873850","summary":null,"start":56885284,"end":56885602,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42624]"}, {"versioned_ensembl_gene_id":"ENSG00000264342.3","gene_symbol":"MIR3660","gene_name":"microRNA 3660 [Source:HGNC Symbol;Acc:HGNC:38985]","synonyms":"hsa-mir-3660","biotype":"miRNA","ncbi_id":"100500825","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90016621,"end":90016720,"strand":-1,"description":"microRNA 3660 [Source:HGNC Symbol;Acc:HGNC:38985]"}, {"versioned_ensembl_gene_id":"ENSG00000207056.1","gene_symbol":"RNU1-8P","gene_name":"RNA, U1 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48307]","synonyms":"RNU1-8","biotype":"snRNA","ncbi_id":"106481604","summary":null,"start":7219360,"end":7219524,"strand":1,"description":"RNA, U1 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48307]"}, {"versioned_ensembl_gene_id":"ENSG00000283971.1","gene_symbol":"MIR4442","gene_name":"microRNA 4442 [Source:HGNC Symbol;Acc:HGNC:41718]","synonyms":"hsa-mir-4442","biotype":"miRNA","ncbi_id":"100616477","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25664873,"end":25664939,"strand":-1,"description":"microRNA 4442 [Source:HGNC Symbol;Acc:HGNC:41718]"}, {"versioned_ensembl_gene_id":"ENSG00000207627.1","gene_symbol":"MIR581","gene_name":"microRNA 581 [Source:HGNC Symbol;Acc:HGNC:32837]","synonyms":"MIRN581,hsa-mir-581","biotype":"miRNA","ncbi_id":"693166","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53951504,"end":53951599,"strand":-1,"description":"microRNA 581 [Source:HGNC Symbol;Acc:HGNC:32837]"}, {"versioned_ensembl_gene_id":"ENSG00000271898.1","gene_symbol":"MIR4791","gene_name":"microRNA 4791 [Source:HGNC Symbol;Acc:HGNC:41704]","synonyms":"hsa-mir-4791","biotype":"miRNA","ncbi_id":"100616291","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19314848,"end":19314931,"strand":-1,"description":"microRNA 4791 [Source:HGNC Symbol;Acc:HGNC:41704]"}, {"versioned_ensembl_gene_id":"ENSG00000273571.1","gene_symbol":"ST7-OT4_2","gene_name":"ST7 overlapping transcript 4 conserved region 2 [Source:RFAM;Acc:RF02188]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116954983,"end":116955154,"strand":1,"description":"ST7 overlapping transcript 4 conserved region 2 [Source:RFAM;Acc:RF02188]"}, {"versioned_ensembl_gene_id":"ENSG00000223324.1","gene_symbol":"RN7SKP273","gene_name":"RNA, 7SK small nuclear pseudogene 273 [Source:HGNC Symbol;Acc:HGNC:45997]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481821","summary":null,"start":111683111,"end":111683424,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 273 [Source:HGNC Symbol;Acc:HGNC:45997]"}, {"versioned_ensembl_gene_id":"ENSG00000283880.1","gene_symbol":"MIR7704","gene_name":"microRNA 7704 [Source:HGNC Symbol;Acc:HGNC:50089]","synonyms":"hsa-mir-7704","biotype":"miRNA","ncbi_id":"102465802","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176188843,"end":176188901,"strand":1,"description":"microRNA 7704 [Source:HGNC Symbol;Acc:HGNC:50089]"}, {"versioned_ensembl_gene_id":"ENSG00000275107.1","gene_symbol":"MIR6782","gene_name":"microRNA 6782 [Source:HGNC Symbol;Acc:HGNC:50270]","synonyms":"hsa-mir-6782","biotype":"miRNA","ncbi_id":"102465469","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44207771,"end":44207839,"strand":-1,"description":"microRNA 6782 [Source:HGNC Symbol;Acc:HGNC:50270]"}, {"versioned_ensembl_gene_id":"ENSG00000206857.1","gene_symbol":"RNU6-214P","gene_name":"RNA, U6 small nuclear 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:47177]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479661","summary":null,"start":120526294,"end":120526400,"strand":-1,"description":"RNA, U6 small nuclear 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:47177]"}, {"versioned_ensembl_gene_id":"ENSG00000284152.1","gene_symbol":"MIR6758","gene_name":"microRNA 6758 [Source:HGNC Symbol;Acc:HGNC:50038]","synonyms":"hsa-mir-6758","biotype":"miRNA","ncbi_id":"102465454","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57512688,"end":57512750,"strand":1,"description":"microRNA 6758 [Source:HGNC Symbol;Acc:HGNC:50038]"}, {"versioned_ensembl_gene_id":"ENSG00000283340.1","gene_symbol":"MIR3119-2","gene_name":"microRNA 3119-2 [Source:HGNC Symbol;Acc:HGNC:38315]","synonyms":"hsa-mir-3119-2","biotype":"miRNA","ncbi_id":"100423010","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":170151378,"end":170151462,"strand":-1,"description":"microRNA 3119-2 [Source:HGNC Symbol;Acc:HGNC:38315]"}, {"versioned_ensembl_gene_id":"ENSG00000212538.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":163923670,"end":163923873,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000266458.1","gene_symbol":"MIR4259","gene_name":"microRNA 4259 [Source:HGNC Symbol;Acc:HGNC:38309]","synonyms":"hsa-mir-4259","biotype":"miRNA","ncbi_id":"100422852","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159899979,"end":159900079,"strand":-1,"description":"microRNA 4259 [Source:HGNC Symbol;Acc:HGNC:38309]"}, {"versioned_ensembl_gene_id":"ENSG00000238926.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72284945,"end":72285045,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271841.1","gene_symbol":"RNU7-10P","gene_name":"RNA, U7 small nuclear 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:34106]","synonyms":"U7.10","biotype":"snRNA","ncbi_id":"100147758","summary":null,"start":17664963,"end":17665025,"strand":1,"description":"RNA, U7 small nuclear 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:34106]"}, {"versioned_ensembl_gene_id":"ENSG00000263987.1","gene_symbol":"MIR5698","gene_name":"microRNA 5698 [Source:HGNC Symbol;Acc:HGNC:43487]","synonyms":"hsa-mir-5698","biotype":"miRNA","ncbi_id":"100847024","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154104521,"end":154104592,"strand":-1,"description":"microRNA 5698 [Source:HGNC Symbol;Acc:HGNC:43487]"}, {"versioned_ensembl_gene_id":"ENSG00000263671.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30795686,"end":30795937,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275968.1","gene_symbol":"DAOA-AS1_1","gene_name":"DAOA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02090]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105459815,"end":105460015,"strand":1,"description":"DAOA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02090]"}, {"versioned_ensembl_gene_id":"ENSG00000207991.1","gene_symbol":"MIR601","gene_name":"microRNA 601 [Source:HGNC Symbol;Acc:HGNC:32857]","synonyms":"MIRN601,hsa-mir-601","biotype":"miRNA","ncbi_id":"693186","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123402525,"end":123402603,"strand":-1,"description":"microRNA 601 [Source:HGNC Symbol;Acc:HGNC:32857]"}, {"versioned_ensembl_gene_id":"ENSG00000279413.1","gene_symbol":"AC112497.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":15702602,"end":15703243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222112.1","gene_symbol":"RN7SKP16","gene_name":"RNA, 7SK small nuclear pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45740]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480837","summary":null,"start":33336566,"end":33336864,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45740]"}, {"versioned_ensembl_gene_id":"ENSG00000221616.1","gene_symbol":"MIR548H4","gene_name":"microRNA 548h-4 [Source:HGNC Symbol;Acc:HGNC:35345]","synonyms":"MIRN548H4,hsa-mir-548h-4","biotype":"miRNA","ncbi_id":"100313884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27048853,"end":27048963,"strand":-1,"description":"microRNA 548h-4 [Source:HGNC Symbol;Acc:HGNC:35345]"}, {"versioned_ensembl_gene_id":"ENSG00000266240.1","gene_symbol":"MIR5091","gene_name":"microRNA 5091 [Source:HGNC Symbol;Acc:HGNC:43478]","synonyms":"hsa-mir-5091","biotype":"miRNA","ncbi_id":"100847023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13627865,"end":13627957,"strand":1,"description":"microRNA 5091 [Source:HGNC Symbol;Acc:HGNC:43478]"}, {"versioned_ensembl_gene_id":"ENSG00000275231.1","gene_symbol":"RMST_4","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 4 [Source:RFAM;Acc:RF01965]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97493897,"end":97494003,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 4 [Source:RFAM;Acc:RF01965]"}, {"versioned_ensembl_gene_id":"ENSG00000252902.1","gene_symbol":"RNA5SP342","gene_name":"RNA, 5S ribosomal pseudogene 342 [Source:HGNC Symbol;Acc:HGNC:43242]","synonyms":"RN5S342","biotype":"rRNA","ncbi_id":"106479008","summary":null,"start":71845196,"end":71845245,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 342 [Source:HGNC Symbol;Acc:HGNC:43242]"}, {"versioned_ensembl_gene_id":"ENSG00000202534.1","gene_symbol":"RNU6-1329P","gene_name":"RNA, U6 small nuclear 1329, pseudogene [Source:HGNC Symbol;Acc:HGNC:48292]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481600","summary":null,"start":92952639,"end":92952745,"strand":1,"description":"RNA, U6 small nuclear 1329, pseudogene [Source:HGNC Symbol;Acc:HGNC:48292]"}, {"versioned_ensembl_gene_id":"ENSG00000238723.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46215070,"end":46215171,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280864.1","gene_symbol":"AC255560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72505075,"end":72550889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284074.1","gene_symbol":"MIR4758","gene_name":"microRNA 4758 [Source:HGNC Symbol;Acc:HGNC:41836]","synonyms":"hsa-mir-4758","biotype":"miRNA","ncbi_id":"100616340","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62332487,"end":62332557,"strand":-1,"description":"microRNA 4758 [Source:HGNC Symbol;Acc:HGNC:41836]"}, {"versioned_ensembl_gene_id":"ENSG00000263750.1","gene_symbol":"MIR548AV","gene_name":"microRNA 548av [Source:HGNC Symbol;Acc:HGNC:43537]","synonyms":"hsa-mir-548av","biotype":"miRNA","ncbi_id":"100847083","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72853321,"end":72853382,"strand":-1,"description":"microRNA 548av [Source:HGNC Symbol;Acc:HGNC:43537]"}, {"versioned_ensembl_gene_id":"ENSG00000200521.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":157768013,"end":157768113,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252943.1","gene_symbol":"RNU6-264P","gene_name":"RNA, U6 small nuclear 264, pseudogene [Source:HGNC Symbol;Acc:HGNC:47227]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481262","summary":null,"start":19073843,"end":19073946,"strand":1,"description":"RNA, U6 small nuclear 264, pseudogene [Source:HGNC Symbol;Acc:HGNC:47227]"}, {"versioned_ensembl_gene_id":"ENSG00000274838.1","gene_symbol":"MIR6788","gene_name":"microRNA 6788 [Source:HGNC Symbol;Acc:HGNC:50078]","synonyms":"hsa-mir-6788","biotype":"miRNA","ncbi_id":"102466735","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10759584,"end":10759649,"strand":-1,"description":"microRNA 6788 [Source:HGNC Symbol;Acc:HGNC:50078]"}, {"versioned_ensembl_gene_id":"ENSG00000243027.3","gene_symbol":"RN7SL354P","gene_name":"RNA, 7SL, cytoplasmic 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:46370]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481838","summary":null,"start":50688900,"end":50689193,"strand":1,"description":"RNA, 7SL, cytoplasmic 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:46370]"}, {"versioned_ensembl_gene_id":"ENSG00000199053.3","gene_symbol":"MIR324","gene_name":"microRNA 324 [Source:HGNC Symbol;Acc:HGNC:31767]","synonyms":"MIRN324,hsa-mir-324","biotype":"miRNA","ncbi_id":"442898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7223297,"end":7223379,"strand":-1,"description":"microRNA 324 [Source:HGNC Symbol;Acc:HGNC:31767]"}, {"versioned_ensembl_gene_id":"ENSG00000201384.1","gene_symbol":"SNORA32","gene_name":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":77201026,"end":77201140,"strand":-1,"description":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]"}, {"versioned_ensembl_gene_id":"ENSG00000278233.1","gene_symbol":"RNA5-8SN5","gene_name":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]","synonyms":null,"biotype":"rRNA","ncbi_id":"100008587","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. This gene is a representative copy of the 5.8S ribosomal RNA whose chromosomal location is unknown. [provided by RefSeq, Mar 2017]","start":8212572,"end":8212724,"strand":1,"description":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]"}, {"versioned_ensembl_gene_id":"ENSG00000207004.1","gene_symbol":"RNU6-301P","gene_name":"RNA, U6 small nuclear 301, pseudogene [Source:HGNC Symbol;Acc:HGNC:47264]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481274","summary":null,"start":51724103,"end":51724209,"strand":1,"description":"RNA, U6 small nuclear 301, pseudogene [Source:HGNC Symbol;Acc:HGNC:47264]"}, {"versioned_ensembl_gene_id":"ENSG00000207749.4","gene_symbol":"MIR299","gene_name":"microRNA 299 [Source:HGNC Symbol;Acc:HGNC:31618]","synonyms":"hsa-mir-299,MIRN299","biotype":"miRNA","ncbi_id":"407023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101023794,"end":101023856,"strand":1,"description":"microRNA 299 [Source:HGNC Symbol;Acc:HGNC:31618]"}, {"versioned_ensembl_gene_id":"ENSG00000202046.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":120192245,"end":120192357,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000259543.1","gene_symbol":"AC060809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81427448,"end":81755217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199082.1","gene_symbol":"MIR342","gene_name":"microRNA 342 [Source:HGNC Symbol;Acc:HGNC:31778]","synonyms":"MIRN342,hsa-mir-342","biotype":"miRNA","ncbi_id":"442909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100109655,"end":100109753,"strand":1,"description":"microRNA 342 [Source:HGNC Symbol;Acc:HGNC:31778]"}, {"versioned_ensembl_gene_id":"ENSG00000252485.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206007880,"end":206007974,"strand":-1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000199453.1","gene_symbol":"SNORD115-12","gene_name":"small nucleolar RNA, C/D box 115-12 [Source:HGNC Symbol;Acc:HGNC:33031]","synonyms":"HBII-52-12","biotype":"snoRNA","ncbi_id":"100033449","summary":null,"start":25191416,"end":25191497,"strand":1,"description":"small nucleolar RNA, C/D box 115-12 [Source:HGNC Symbol;Acc:HGNC:33031]"}, {"versioned_ensembl_gene_id":"ENSG00000283126.1","gene_symbol":"MIR1297","gene_name":"microRNA 1297 [Source:HGNC Symbol;Acc:HGNC:35289]","synonyms":"hsa-mir-1297,MIRN1297","biotype":"miRNA","ncbi_id":"100302187","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8388362,"end":8388453,"strand":1,"description":"microRNA 6724-3 [Source:HGNC Symbol;Acc:HGNC:50842]"}, {"versioned_ensembl_gene_id":"ENSG00000265595.1","gene_symbol":"MIR4756","gene_name":"microRNA 4756 [Source:HGNC Symbol;Acc:HGNC:41529]","synonyms":"hsa-mir-4756","biotype":"miRNA","ncbi_id":"100616225","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54068408,"end":54068485,"strand":-1,"description":"microRNA 4756 [Source:HGNC Symbol;Acc:HGNC:41529]"}, {"versioned_ensembl_gene_id":"ENSG00000251724.1","gene_symbol":"RNU7-175P","gene_name":"RNA, U7 small nuclear 175 pseudogene [Source:HGNC Symbol;Acc:HGNC:45709]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479091","summary":null,"start":75538598,"end":75538658,"strand":-1,"description":"RNA, U7 small nuclear 175 pseudogene [Source:HGNC Symbol;Acc:HGNC:45709]"}, {"versioned_ensembl_gene_id":"ENSG00000263529.2","gene_symbol":"RN7SL122P","gene_name":"RNA, 7SL, cytoplasmic 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:46138]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480954","summary":null,"start":32457835,"end":32458135,"strand":1,"description":"RNA, 7SL, cytoplasmic 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:46138]"}, {"versioned_ensembl_gene_id":"ENSG00000252777.1","gene_symbol":"SCARNA24","gene_name":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]","synonyms":null,"biotype":"scaRNA","ncbi_id":null,"summary":null,"start":28689665,"end":28689794,"strand":1,"description":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]"}, {"versioned_ensembl_gene_id":"ENSG00000283455.1","gene_symbol":"MIR523","gene_name":"microRNA 523 [Source:HGNC Symbol;Acc:HGNC:32103]","synonyms":"MIRN523,hsa-mir-523","biotype":"miRNA","ncbi_id":"574471","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53698385,"end":53698471,"strand":1,"description":"microRNA 523 [Source:HGNC Symbol;Acc:HGNC:32103]"}, {"versioned_ensembl_gene_id":"ENSG00000239910.3","gene_symbol":"RN7SL530P","gene_name":"RNA, 7SL, cytoplasmic 530, pseudogene [Source:HGNC Symbol;Acc:HGNC:46546]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481067","summary":null,"start":74174456,"end":74174753,"strand":1,"description":"RNA, 7SL, cytoplasmic 530, pseudogene [Source:HGNC Symbol;Acc:HGNC:46546]"}, {"versioned_ensembl_gene_id":"ENSG00000251996.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7341531,"end":7341642,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283502.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":47781379,"end":47781465,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000215930.1","gene_symbol":"MIR942","gene_name":"microRNA 942 [Source:HGNC Symbol;Acc:HGNC:33688]","synonyms":"MIRN942,hsa-mir-942","biotype":"miRNA","ncbi_id":"100126331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":117094643,"end":117094728,"strand":1,"description":"microRNA 942 [Source:HGNC Symbol;Acc:HGNC:33688]"}, {"versioned_ensembl_gene_id":"ENSG00000207754.3","gene_symbol":"MIR487B","gene_name":"microRNA 487b [Source:HGNC Symbol;Acc:HGNC:32533]","synonyms":"MIRN487B,hsa-mir-487b","biotype":"miRNA","ncbi_id":"664616","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101046455,"end":101046538,"strand":1,"description":"microRNA 487b [Source:HGNC Symbol;Acc:HGNC:32533]"}, {"versioned_ensembl_gene_id":"ENSG00000281696.1","gene_symbol":"MIR664A","gene_name":"microRNA 664a [Source:HGNC Symbol;Acc:HGNC:35370]","synonyms":"MIRN664,MIR664,hsa-mir-664","biotype":"miRNA","ncbi_id":"100302234","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":220200538,"end":220200619,"strand":-1,"description":"microRNA 664a [Source:HGNC Symbol;Acc:HGNC:35370]"}, {"versioned_ensembl_gene_id":"ENSG00000275878.1","gene_symbol":"RN7SL43P","gene_name":"RNA, 7SL, cytoplasmic 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46059]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479241","summary":null,"start":66980120,"end":66980410,"strand":1,"description":"RNA, 7SL, cytoplasmic 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46059]"}, {"versioned_ensembl_gene_id":"ENSG00000200885.1","gene_symbol":"RNU1-146P","gene_name":"RNA, U1 small nuclear 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:48488]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480198","summary":null,"start":19724435,"end":19724599,"strand":1,"description":"RNA, U1 small nuclear 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:48488]"}, {"versioned_ensembl_gene_id":"ENSG00000274409.1","gene_symbol":"DLX6-AS1_1","gene_name":"Embryonic ventral forebrain RNA 1 conserved region 1 [Source:RFAM;Acc:RF01887]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96965302,"end":96965481,"strand":1,"description":"Embryonic ventral forebrain RNA 1 conserved region 1 [Source:RFAM;Acc:RF01887]"}, {"versioned_ensembl_gene_id":"ENSG00000200403.1","gene_symbol":"RNU6-1099P","gene_name":"RNA, U6 small nuclear 1099, pseudogene [Source:HGNC Symbol;Acc:HGNC:48062]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481526","summary":null,"start":19305076,"end":19305182,"strand":-1,"description":"RNA, U6 small nuclear 1099, pseudogene [Source:HGNC Symbol;Acc:HGNC:48062]"}, {"versioned_ensembl_gene_id":"ENSG00000199337.1","gene_symbol":"RNA5S3","gene_name":"RNA, 5S ribosomal 3 [Source:HGNC Symbol;Acc:HGNC:34364]","synonyms":"RN5S3","biotype":"rRNA","ncbi_id":"100169754","summary":null,"start":228614750,"end":228614868,"strand":-1,"description":"RNA, 5S ribosomal 3 [Source:HGNC Symbol;Acc:HGNC:34364]"}, {"versioned_ensembl_gene_id":"ENSG00000273744.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":106271634,"end":106271720,"strand":1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000274799.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":148389748,"end":148390029,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207109.1","gene_symbol":"SNORD38C","gene_name":"small nucleolar RNA, C/D box 38C [Source:HGNC Symbol;Acc:HGNC:52227]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617024","summary":null,"start":53333060,"end":53333128,"strand":-1,"description":"small nucleolar RNA, C/D box 38C [Source:HGNC Symbol;Acc:HGNC:52227]"}, {"versioned_ensembl_gene_id":"ENSG00000206847.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129030459,"end":129030572,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252065.1","gene_symbol":"RNU6-864P","gene_name":"RNA, U6 small nuclear 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:47827]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481776","summary":null,"start":28982303,"end":28982410,"strand":-1,"description":"RNA, U6 small nuclear 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:47827]"}, {"versioned_ensembl_gene_id":"ENSG00000274055.1","gene_symbol":"CDKN2B-AS_3","gene_name":"CDKN2B antisense RNA 1 convserved region 3 [Source:RFAM;Acc:RF02045]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22046758,"end":22046901,"strand":1,"description":"CDKN2B antisense RNA 1 convserved region 3 [Source:RFAM;Acc:RF02045]"}, {"versioned_ensembl_gene_id":"ENSG00000272160.1","gene_symbol":"RNU4-5P","gene_name":"RNA, U4 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10198]","synonyms":"U4/6,U4,RNU4P5","biotype":"snRNA","ncbi_id":"26839","summary":null,"start":109869858,"end":109869992,"strand":1,"description":"RNA, U4 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10198]"}, {"versioned_ensembl_gene_id":"ENSG00000209482.1","gene_symbol":"SNORD83A","gene_name":"small nucleolar RNA, C/D box 83A [Source:HGNC Symbol;Acc:HGNC:17131]","synonyms":"U83A,RNU83A","biotype":"snoRNA","ncbi_id":"116937","summary":"Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83A, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83A, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39315213,"end":39315307,"strand":-1,"description":"small nucleolar RNA, C/D box 83A [Source:HGNC Symbol;Acc:HGNC:17131]"}, {"versioned_ensembl_gene_id":"ENSG00000206758.1","gene_symbol":"RNU6-317P","gene_name":"RNA, U6 small nuclear 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:47280]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479708","summary":null,"start":48793152,"end":48793258,"strand":-1,"description":"RNA, U6 small nuclear 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:47280]"}, {"versioned_ensembl_gene_id":"ENSG00000264271.2","gene_symbol":"RN7SL488P","gene_name":"RNA, 7SL, cytoplasmic 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:46504]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479401","summary":null,"start":63529613,"end":63529898,"strand":-1,"description":"RNA, 7SL, cytoplasmic 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:46504]"}, {"versioned_ensembl_gene_id":"ENSG00000238391.1","gene_symbol":"RNA5SP233","gene_name":"RNA, 5S ribosomal pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:43133]","synonyms":"RN5S233","biotype":"rRNA","ncbi_id":"100873491","summary":null,"start":74487428,"end":74487540,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:43133]"}, {"versioned_ensembl_gene_id":"ENSG00000201348.1","gene_symbol":"RNU105B","gene_name":"RNA, U105B small nucleolar [Source:HGNC Symbol;Acc:HGNC:10103]","synonyms":"E1-2","biotype":"snoRNA","ncbi_id":"26767","summary":null,"start":8831186,"end":8831393,"strand":1,"description":"RNA, U105B small nucleolar [Source:HGNC Symbol;Acc:HGNC:10103]"}, {"versioned_ensembl_gene_id":"ENSG00000244139.3","gene_symbol":"RN7SL397P","gene_name":"RNA, 7SL, cytoplasmic 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:46413]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479369","summary":null,"start":120121909,"end":120122206,"strand":1,"description":"RNA, 7SL, cytoplasmic 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:46413]"}, {"versioned_ensembl_gene_id":"ENSG00000222123.1","gene_symbol":"RNA5SP390","gene_name":"RNA, 5S ribosomal pseudogene 390 [Source:HGNC Symbol;Acc:HGNC:43290]","synonyms":"RN5S390","biotype":"rRNA","ncbi_id":"100873643","summary":null,"start":25738508,"end":25738620,"strand":1,"description":"RNA, 5S ribosomal pseudogene 390 [Source:HGNC Symbol;Acc:HGNC:43290]"}, {"versioned_ensembl_gene_id":"ENSG00000281614.2","gene_symbol":"INPP5D","gene_name":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]","synonyms":"SHIP,hp51CN,SHIP1","biotype":"protein_coding","ncbi_id":"3635","summary":"This gene is a member of the inositol polyphosphate-5-phosphatase (INPP5) family and encodes a protein with an N-terminal SH2 domain, an inositol phosphatase domain, and two C-terminal protein interaction domains. Expression of this protein is restricted to hematopoietic cells where its movement from the cytosol to the plasma membrane is mediated by tyrosine phosphorylation. At the plasma membrane, the protein hydrolyzes the 5' phosphate from phosphatidylinositol (3,4,5)-trisphosphate and inositol-1,3,4,5-tetrakisphosphate, thereby affecting multiple signaling pathways. The protein is also partly localized to the nucleus, where it may be involved in nuclear inositol phosphate signaling processes. Overall, the protein functions as a negative regulator of myeloid cell proliferation and survival. Mutations in this gene are associated with defects and cancers of the immune system. Deficiencies in the encoded protein, SHIP1, have been associated with Inflammatory Bowel Disease types such as Crohn's Disease and Ulcerative Colitis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":233059967,"end":233207903,"strand":1,"description":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]"}, {"versioned_ensembl_gene_id":"ENSG00000274380.1","gene_symbol":"MIR6801","gene_name":"microRNA 6801 [Source:HGNC Symbol;Acc:HGNC:50178]","synonyms":"hsa-mir-6801","biotype":"miRNA","ncbi_id":"102466984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52222020,"end":52222098,"strand":1,"description":"microRNA 6801 [Source:HGNC Symbol;Acc:HGNC:50178]"}, {"versioned_ensembl_gene_id":"ENSG00000202479.1","gene_symbol":"SNORD14","gene_name":"Small nucleolar RNA SNORD14 [Source:RFAM;Acc:RF00016]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":24969388,"end":24969477,"strand":-1,"description":"Small nucleolar RNA SNORD14 [Source:RFAM;Acc:RF00016]"}, {"versioned_ensembl_gene_id":"ENSG00000265154.1","gene_symbol":"MIR151B","gene_name":"microRNA 151b [Source:HGNC Symbol;Acc:HGNC:41588]","synonyms":"hsa-mir-151b","biotype":"miRNA","ncbi_id":"100616247","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100109419,"end":100109514,"strand":-1,"description":"microRNA 151b [Source:HGNC Symbol;Acc:HGNC:41588]"}, {"versioned_ensembl_gene_id":"ENSG00000252964.1","gene_symbol":"RNA5SP400","gene_name":"RNA, 5S ribosomal pseudogene 400 [Source:HGNC Symbol;Acc:HGNC:43300]","synonyms":"RN5S400","biotype":"rRNA","ncbi_id":"100873653","summary":null,"start":86138269,"end":86138379,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 400 [Source:HGNC Symbol;Acc:HGNC:43300]"}, {"versioned_ensembl_gene_id":"ENSG00000252537.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":16005808,"end":16005923,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000206592.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":79220942,"end":79221073,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000238443.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133238455,"end":133238549,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252487.1","gene_symbol":"RNY4P20","gene_name":"RNA, Ro-associated Y4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:34070]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379378","summary":null,"start":151298841,"end":151298933,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:34070]"}, {"versioned_ensembl_gene_id":"ENSG00000252342.1","gene_symbol":"RNA5SP164","gene_name":"RNA, 5S ribosomal pseudogene 164 [Source:HGNC Symbol;Acc:HGNC:43064]","synonyms":"RN5S164","biotype":"rRNA","ncbi_id":"100873429","summary":null,"start":93820171,"end":93820280,"strand":1,"description":"RNA, 5S ribosomal pseudogene 164 [Source:HGNC Symbol;Acc:HGNC:43064]"}, {"versioned_ensembl_gene_id":"ENSG00000201624.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33982465,"end":33982566,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252944.1","gene_symbol":"RNU6-897P","gene_name":"RNA, U6 small nuclear 897, pseudogene [Source:HGNC Symbol;Acc:HGNC:47860]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479963","summary":null,"start":104766822,"end":104766926,"strand":1,"description":"RNA, U6 small nuclear 897, pseudogene [Source:HGNC Symbol;Acc:HGNC:47860]"}, {"versioned_ensembl_gene_id":"ENSG00000264997.1","gene_symbol":"SNORD39","gene_name":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":109263494,"end":109263564,"strand":-1,"description":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]"}, {"versioned_ensembl_gene_id":"ENSG00000233737.3","gene_symbol":"AP003072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93221486,"end":93221630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207975.1","gene_symbol":"MIR181B1","gene_name":"microRNA 181b-1 [Source:HGNC Symbol;Acc:HGNC:31550]","synonyms":"MIRN181B1,hsa-mir-181b-1","biotype":"miRNA","ncbi_id":"406955","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12719132,"end":12719190,"strand":1,"description":"microRNA 5692a-2 [Source:HGNC Symbol;Acc:HGNC:43466]"}, {"versioned_ensembl_gene_id":"ENSG00000201782.1","gene_symbol":"RN7SKP226","gene_name":"RNA, 7SK small nuclear pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:45950]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480903","summary":null,"start":128220504,"end":128220803,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:45950]"}, {"versioned_ensembl_gene_id":"ENSG00000199878.1","gene_symbol":"RN7SKP149","gene_name":"RNA, 7SK small nuclear pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:45873]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479161","summary":null,"start":143197248,"end":143197591,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:45873]"}, {"versioned_ensembl_gene_id":"ENSG00000201600.1","gene_symbol":"RN7SKP124","gene_name":"RNA, 7SK small nuclear pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:45848]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480871","summary":null,"start":139584105,"end":139584445,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:45848]"}, {"versioned_ensembl_gene_id":"ENSG00000252977.1","gene_symbol":"RNA5SP70","gene_name":"RNA, 5S ribosomal pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:42847]","synonyms":"RN5S70","biotype":"rRNA","ncbi_id":"106480436","summary":null,"start":181771566,"end":181771644,"strand":1,"description":"RNA, 5S ribosomal pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:42847]"}, {"versioned_ensembl_gene_id":"ENSG00000207022.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":92846059,"end":92846182,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000276575.1","gene_symbol":"MIR6895","gene_name":"microRNA 6895 [Source:HGNC Symbol;Acc:HGNC:50210]","synonyms":"hsa-mir-6895","biotype":"miRNA","ncbi_id":"102465539","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53195411,"end":53195488,"strand":-1,"description":"microRNA 6895 [Source:HGNC Symbol;Acc:HGNC:50210]"}, {"versioned_ensembl_gene_id":"ENSG00000207716.1","gene_symbol":"MIR572","gene_name":"microRNA 572 [Source:HGNC Symbol;Acc:HGNC:32828]","synonyms":"MIRN572,hsa-mir-572","biotype":"miRNA","ncbi_id":"693157","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11368827,"end":11368921,"strand":1,"description":"microRNA 572 [Source:HGNC Symbol;Acc:HGNC:32828]"}, {"versioned_ensembl_gene_id":"ENSG00000264814.1","gene_symbol":"MIR1273C","gene_name":"microRNA 1273c [Source:HGNC Symbol;Acc:HGNC:38173]","synonyms":"hsa-mir-1273c","biotype":"miRNA","ncbi_id":"100422821","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154853360,"end":154853436,"strand":1,"description":"microRNA 1273c [Source:HGNC Symbol;Acc:HGNC:38173]"}, {"versioned_ensembl_gene_id":"ENSG00000252692.1","gene_symbol":"SNORD60","gene_name":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]","synonyms":"U60,RNU60","biotype":"snoRNA","ncbi_id":"26788","summary":null,"start":206080239,"end":206080324,"strand":1,"description":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]"}, {"versioned_ensembl_gene_id":"ENSG00000200839.1","gene_symbol":"RNA5SP48","gene_name":"RNA, 5S ribosomal pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:42824]","synonyms":"RN5S48","biotype":"rRNA","ncbi_id":"100873287","summary":null,"start":51973410,"end":51973535,"strand":1,"description":"RNA, 5S ribosomal pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:42824]"}, {"versioned_ensembl_gene_id":"ENSG00000242170.3","gene_symbol":"RN7SL329P","gene_name":"RNA, 7SL, cytoplasmic 329, pseudogene [Source:HGNC Symbol;Acc:HGNC:46345]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479343","summary":null,"start":125270604,"end":125270902,"strand":1,"description":"RNA, 7SL, cytoplasmic 329, pseudogene [Source:HGNC Symbol;Acc:HGNC:46345]"}, {"versioned_ensembl_gene_id":"ENSG00000263669.2","gene_symbol":"RN7SL470P","gene_name":"RNA, 7SL, cytoplasmic 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:46486]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479394","summary":null,"start":70075014,"end":70075272,"strand":-1,"description":"RNA, 7SL, cytoplasmic 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:46486]"}, {"versioned_ensembl_gene_id":"ENSG00000199322.1","gene_symbol":"RNA5SP183","gene_name":"RNA, 5S ribosomal pseudogene 183 [Source:HGNC Symbol;Acc:HGNC:43083]","synonyms":"RN5S183","biotype":"rRNA","ncbi_id":"100873445","summary":null,"start":55777469,"end":55777587,"strand":1,"description":"RNA, 5S ribosomal pseudogene 183 [Source:HGNC Symbol;Acc:HGNC:43083]"}, {"versioned_ensembl_gene_id":"ENSG00000212365.1","gene_symbol":"RNA5SP332","gene_name":"RNA, 5S ribosomal pseudogene 332 [Source:HGNC Symbol;Acc:HGNC:43232]","synonyms":"RN5S332","biotype":"rRNA","ncbi_id":"100873598","summary":null,"start":14134986,"end":14135100,"strand":1,"description":"RNA, 5S ribosomal pseudogene 332 [Source:HGNC Symbol;Acc:HGNC:43232]"}, {"versioned_ensembl_gene_id":"ENSG00000244710.3","gene_symbol":"RN7SL47P","gene_name":"RNA, 7SL, cytoplasmic 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46063]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479242","summary":null,"start":106283413,"end":106283711,"strand":-1,"description":"RNA, 7SL, cytoplasmic 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46063]"}, {"versioned_ensembl_gene_id":"ENSG00000238880.1","gene_symbol":"RNU7-59P","gene_name":"RNA, U7 small nuclear 59 pseudogene [Source:HGNC Symbol;Acc:HGNC:34155]","synonyms":"U7.59","biotype":"snRNA","ncbi_id":"100151654","summary":null,"start":77566934,"end":77566994,"strand":-1,"description":"RNA, U7 small nuclear 59 pseudogene [Source:HGNC Symbol;Acc:HGNC:34155]"}, {"versioned_ensembl_gene_id":"ENSG00000278340.1","gene_symbol":"MIR6862-2","gene_name":"microRNA 6862-2 [Source:HGNC Symbol;Acc:HGNC:50192]","synonyms":"hsa-mir-6862-2","biotype":"miRNA","ncbi_id":"102465907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28724252,"end":28724321,"strand":1,"description":"microRNA 6862-2 [Source:HGNC Symbol;Acc:HGNC:50192]"}, {"versioned_ensembl_gene_id":"ENSG00000200314.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":106454828,"end":106454929,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264530.2","gene_symbol":"RN7SL25P","gene_name":"RNA, 7SL, cytoplasmic 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46041]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479233","summary":null,"start":6542094,"end":6542353,"strand":1,"description":"RNA, 7SL, cytoplasmic 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46041]"}, {"versioned_ensembl_gene_id":"ENSG00000201493.1","gene_symbol":"RNU1-141P","gene_name":"RNA, U1 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:48483]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481633","summary":null,"start":218129795,"end":218129952,"strand":1,"description":"RNA, U1 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:48483]"}, {"versioned_ensembl_gene_id":"ENSG00000252443.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"RNU108,E2,RNE2,E2-1","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":69785994,"end":69786113,"strand":-1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000241542.3","gene_symbol":"RN7SL369P","gene_name":"RNA, 7SL, cytoplasmic 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:46385]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480694","summary":null,"start":67705954,"end":67706252,"strand":1,"description":"RNA, 7SL, cytoplasmic 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:46385]"}, {"versioned_ensembl_gene_id":"ENSG00000212348.1","gene_symbol":"RNU6-1300P","gene_name":"RNA, U6 small nuclear 1300, pseudogene [Source:HGNC Symbol;Acc:HGNC:48263]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480134","summary":null,"start":74048677,"end":74048784,"strand":1,"description":"RNA, U6 small nuclear 1300, pseudogene [Source:HGNC Symbol;Acc:HGNC:48263]"}, {"versioned_ensembl_gene_id":"ENSG00000207935.3","gene_symbol":"MIR204","gene_name":"microRNA 204 [Source:HGNC Symbol;Acc:HGNC:31582]","synonyms":"MIRN204,hsa-mir-204","biotype":"miRNA","ncbi_id":"406987","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70809975,"end":70810084,"strand":-1,"description":"microRNA 204 [Source:HGNC Symbol;Acc:HGNC:31582]"}, {"versioned_ensembl_gene_id":"ENSG00000221269.1","gene_symbol":"MIR1302-8","gene_name":"microRNA 1302-8 [Source:HGNC Symbol;Acc:HGNC:35300]","synonyms":"MIRN1302-8,hsa-mir-1302-8","biotype":"miRNA","ncbi_id":"100302223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97363554,"end":97363681,"strand":-1,"description":"microRNA 1302-8 [Source:HGNC Symbol;Acc:HGNC:35300]"}, {"versioned_ensembl_gene_id":"ENSG00000207116.1","gene_symbol":"RNU6-31P","gene_name":"RNA, U6 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:34250]","synonyms":"RNU6-31","biotype":"snRNA","ncbi_id":"100873740","summary":null,"start":200830009,"end":200830116,"strand":1,"description":"RNA, U6 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:34250]"}, {"versioned_ensembl_gene_id":"ENSG00000238721.1","gene_symbol":"RNU7-194P","gene_name":"RNA, U7 small nuclear 194 pseudogene [Source:HGNC Symbol;Acc:HGNC:45728]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480834","summary":null,"start":150209706,"end":150209768,"strand":1,"description":"RNA, U7 small nuclear 194 pseudogene [Source:HGNC Symbol;Acc:HGNC:45728]"}, {"versioned_ensembl_gene_id":"ENSG00000207165.1","gene_symbol":"SNORA70","gene_name":"small nucleolar RNA, H/ACA box 70 [Source:HGNC Symbol;Acc:HGNC:10231]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":154400281,"end":154400415,"strand":1,"description":"small nucleolar RNA, H/ACA box 70 [Source:HGNC Symbol;Acc:HGNC:10231]"}, {"versioned_ensembl_gene_id":"ENSG00000222859.1","gene_symbol":"RN7SKP136","gene_name":"RNA, 7SK small nuclear pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:45860]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479155","summary":null,"start":177181442,"end":177181741,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:45860]"}, {"versioned_ensembl_gene_id":"ENSG00000272055.1","gene_symbol":"RNU6-6P","gene_name":"RNA, U6 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:10228]","synonyms":"U6-6,RNU6B,RNU6-6","biotype":"snRNA","ncbi_id":"26826","summary":null,"start":13217269,"end":13217375,"strand":1,"description":"RNA, U6 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:10228]"}, {"versioned_ensembl_gene_id":"ENSG00000207138.1","gene_symbol":"RNU6-869P","gene_name":"RNA, U6 small nuclear 869, pseudogene [Source:HGNC Symbol;Acc:HGNC:47832]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480616","summary":null,"start":126504763,"end":126504869,"strand":1,"description":"RNA, U6 small nuclear 869, pseudogene [Source:HGNC Symbol;Acc:HGNC:47832]"}, {"versioned_ensembl_gene_id":"ENSG00000278712.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34,SEN34L,SEN34L,LENG5,LENG5,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000199400.1","gene_symbol":"RNY4P19","gene_name":"RNA, Ro-associated Y4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:34069]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100169834","summary":null,"start":230058229,"end":230058324,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:34069]"}, {"versioned_ensembl_gene_id":"ENSG00000251759.1","gene_symbol":"RN7SKP298","gene_name":"RNA, 7SK small nuclear pseudogene 298 [Source:HGNC Symbol;Acc:HGNC:46022]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479228","summary":null,"start":166670029,"end":166670122,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 298 [Source:HGNC Symbol;Acc:HGNC:46022]"}, {"versioned_ensembl_gene_id":"ENSG00000251991.1","gene_symbol":"RNU7-49P","gene_name":"RNA, U7 small nuclear 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:34145]","synonyms":"U7.49","biotype":"snRNA","ncbi_id":"100147836","summary":null,"start":14478892,"end":14478953,"strand":1,"description":"RNA, U7 small nuclear 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:34145]"}, {"versioned_ensembl_gene_id":"ENSG00000277188.1","gene_symbol":"NCRUPAR_1","gene_name":"Non-protein coding RNA, upstream of F2R/PAR1 conserved region 1 [Source:RFAM;Acc:RF02154]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76712195,"end":76712327,"strand":1,"description":"Non-protein coding RNA, upstream of F2R/PAR1 conserved region 1 [Source:RFAM;Acc:RF02154]"}, {"versioned_ensembl_gene_id":"ENSG00000264879.2","gene_symbol":"RN7SL690P","gene_name":"RNA, 7SL, cytoplasmic 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:46706]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479475","summary":null,"start":20316755,"end":20316994,"strand":1,"description":"RNA, 7SL, cytoplasmic 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:46706]"}, {"versioned_ensembl_gene_id":"ENSG00000207705.2","gene_symbol":"MIR129-1","gene_name":"microRNA 129-1 [Source:HGNC Symbol;Acc:HGNC:31512]","synonyms":"MIRN129-1,hsa-mir-129-1","biotype":"miRNA","ncbi_id":"406917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128207872,"end":128207943,"strand":1,"description":"microRNA 129-1 [Source:HGNC Symbol;Acc:HGNC:31512]"}, {"versioned_ensembl_gene_id":"ENSG00000201856.1","gene_symbol":"RNA5SP331","gene_name":"RNA, 5S ribosomal pseudogene 331 [Source:HGNC Symbol;Acc:HGNC:43231]","synonyms":"RN5S331","biotype":"rRNA","ncbi_id":"100873597","summary":null,"start":13907484,"end":13907590,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 331 [Source:HGNC Symbol;Acc:HGNC:43231]"}, {"versioned_ensembl_gene_id":"ENSG00000200238.1","gene_symbol":"RNA5SP133","gene_name":"RNA, 5S ribosomal pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:43033]","synonyms":"RN5S133","biotype":"rRNA","ncbi_id":"100873402","summary":null,"start":56185104,"end":56185222,"strand":1,"description":"RNA, 5S ribosomal pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:43033]"}, {"versioned_ensembl_gene_id":"ENSG00000201311.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":82307067,"end":82307168,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240905.3","gene_symbol":"RN7SL798P","gene_name":"RNA, 7SL, cytoplasmic 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:46814]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480533","summary":null,"start":55980240,"end":55980540,"strand":-1,"description":"RNA, 7SL, cytoplasmic 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:46814]"}, {"versioned_ensembl_gene_id":"ENSG00000271150.1","gene_symbol":"AC008745.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47794650,"end":47794920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274705.2","gene_symbol":"MIR486-1","gene_name":"microRNA 486-1 [Source:HGNC Symbol;Acc:HGNC:32342]","synonyms":"MIRN486,MIR486,hsa-mir-486","biotype":"miRNA","ncbi_id":"619554","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41660441,"end":41660508,"strand":-1,"description":"microRNA 486-1 [Source:HGNC Symbol;Acc:HGNC:32342]"}, {"versioned_ensembl_gene_id":"ENSG00000266320.1","gene_symbol":"MIR3909","gene_name":"microRNA 3909 [Source:HGNC Symbol;Acc:HGNC:38987]","synonyms":"hsa-mir-3909","biotype":"miRNA","ncbi_id":"100500826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35335640,"end":35335758,"strand":1,"description":"microRNA 3909 [Source:HGNC Symbol;Acc:HGNC:38987]"}, {"versioned_ensembl_gene_id":"ENSG00000262104.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78544095,"end":78544188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284407.1","gene_symbol":"MIR5001","gene_name":"microRNA 5001 [Source:HGNC Symbol;Acc:HGNC:43462]","synonyms":"hsa-mir-5001","biotype":"miRNA","ncbi_id":"100847037","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":232550474,"end":232550573,"strand":-1,"description":"microRNA 5001 [Source:HGNC Symbol;Acc:HGNC:43462]"}, {"versioned_ensembl_gene_id":"ENSG00000201822.1","gene_symbol":"RNA5SP149","gene_name":"RNA, 5S ribosomal pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:43049]","synonyms":"RN5S149","biotype":"rRNA","ncbi_id":"106480437","summary":null,"start":180161886,"end":180161977,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 149 [Source:HGNC Symbol;Acc:HGNC:43049]"}, {"versioned_ensembl_gene_id":"ENSG00000277904.1","gene_symbol":"MIR7850","gene_name":"microRNA 7850 [Source:HGNC Symbol;Acc:HGNC:50118]","synonyms":"hsa-mir-7850","biotype":"miRNA","ncbi_id":"102465838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2630715,"end":2630793,"strand":1,"description":"microRNA 7850 [Source:HGNC Symbol;Acc:HGNC:50118]"}, {"versioned_ensembl_gene_id":"ENSG00000208002.1","gene_symbol":"MIR643","gene_name":"microRNA 643 [Source:HGNC Symbol;Acc:HGNC:32899]","synonyms":"MIRN643,hsa-mir-643","biotype":"miRNA","ncbi_id":"693228","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52281797,"end":52281893,"strand":1,"description":"microRNA 643 [Source:HGNC Symbol;Acc:HGNC:32899]"}, {"versioned_ensembl_gene_id":"ENSG00000244296.3","gene_symbol":"RN7SL168P","gene_name":"RNA, 7SL, cytoplasmic 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:46184]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480491","summary":null,"start":19365766,"end":19366044,"strand":1,"description":"RNA, 7SL, cytoplasmic 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:46184]"}, {"versioned_ensembl_gene_id":"ENSG00000276281.1","gene_symbol":"RN7SL126P","gene_name":"RNA, 7SL, cytoplasmic 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:46142]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479268","summary":null,"start":85567662,"end":85567960,"strand":-1,"description":"RNA, 7SL, cytoplasmic 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:46142]"}, {"versioned_ensembl_gene_id":"ENSG00000201428.1","gene_symbol":"RN7SKP71","gene_name":"RNA, 7SK small nuclear pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:45795]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479126","summary":null,"start":112267077,"end":112267394,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:45795]"}, {"versioned_ensembl_gene_id":"ENSG00000207390.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44697333,"end":44697430,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206747.1","gene_symbol":"RNU6-245P","gene_name":"RNA, U6 small nuclear 245, pseudogene [Source:HGNC Symbol;Acc:HGNC:47208]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481255","summary":null,"start":68539443,"end":68539549,"strand":-1,"description":"RNA, U6 small nuclear 245, pseudogene [Source:HGNC Symbol;Acc:HGNC:47208]"}, {"versioned_ensembl_gene_id":"ENSG00000199237.1","gene_symbol":"RNU6-834P","gene_name":"RNA, U6 small nuclear 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:47797]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479935","summary":null,"start":49593104,"end":49593213,"strand":1,"description":"RNA, U6 small nuclear 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:47797]"}, {"versioned_ensembl_gene_id":"ENSG00000238962.1","gene_symbol":"RNU7-176P","gene_name":"RNA, U7 small nuclear 176 pseudogene [Source:HGNC Symbol;Acc:HGNC:45710]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481803","summary":null,"start":10815485,"end":10815546,"strand":-1,"description":"RNA, U7 small nuclear 176 pseudogene [Source:HGNC Symbol;Acc:HGNC:45710]"}, {"versioned_ensembl_gene_id":"ENSG00000242080.1","gene_symbol":"AC008571.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152495718,"end":152496017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284219.1","gene_symbol":"MIR202","gene_name":"microRNA 202 [Source:HGNC Symbol;Acc:HGNC:32080]","synonyms":"MIRN202,hsa-mir-202","biotype":"miRNA","ncbi_id":"574448","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133247511,"end":133247620,"strand":-1,"description":"microRNA 202 [Source:HGNC Symbol;Acc:HGNC:32080]"}, {"versioned_ensembl_gene_id":"ENSG00000251964.2","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":14643787,"end":14643848,"strand":1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000252752.1","gene_symbol":"RNU6-210P","gene_name":"RNA, U6 small nuclear 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:47173]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479659","summary":null,"start":93010257,"end":93010351,"strand":1,"description":"RNA, U6 small nuclear 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:47173]"}, {"versioned_ensembl_gene_id":"ENSG00000274819.1","gene_symbol":"RMST_7","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 7 [Source:RFAM;Acc:RF01968]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97532691,"end":97532958,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 7 [Source:RFAM;Acc:RF01968]"}, {"versioned_ensembl_gene_id":"ENSG00000199605.1","gene_symbol":"RNY4P24","gene_name":"RNA, Ro-associated Y4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42474]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862664","summary":null,"start":52400004,"end":52400099,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42474]"}, {"versioned_ensembl_gene_id":"ENSG00000278802.1","gene_symbol":"RMST_8","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 8 [Source:RFAM;Acc:RF01969]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97560557,"end":97560721,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 8 [Source:RFAM;Acc:RF01969]"}, {"versioned_ensembl_gene_id":"ENSG00000251943.1","gene_symbol":"RNU6-693P","gene_name":"RNA, U6 small nuclear 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:47656]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481399","summary":null,"start":172613428,"end":172613534,"strand":-1,"description":"RNA, U6 small nuclear 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:47656]"}, {"versioned_ensembl_gene_id":"ENSG00000277776.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54931214,"end":54955210,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000206781.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64445130,"end":64445243,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000271922.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":154329716,"end":154329819,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000275337.1","gene_symbol":"RN7SL680P","gene_name":"RNA, 7SL, cytoplasmic 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:46696]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480380","summary":null,"start":39349094,"end":39349392,"strand":-1,"description":"RNA, 7SL, cytoplasmic 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:46696]"}, {"versioned_ensembl_gene_id":"ENSG00000253093.1","gene_symbol":"RNA5SP179","gene_name":"RNA, 5S ribosomal pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:43079]","synonyms":"RN5S179","biotype":"rRNA","ncbi_id":"100873441","summary":null,"start":16853994,"end":16854114,"strand":1,"description":"RNA, 5S ribosomal pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:43079]"}, {"versioned_ensembl_gene_id":"ENSG00000239607.3","gene_symbol":"RN7SL573P","gene_name":"RNA, 7SL, cytoplasmic 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:46589]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481078","summary":null,"start":75041740,"end":75042015,"strand":1,"description":"RNA, 7SL, cytoplasmic 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:46589]"}, {"versioned_ensembl_gene_id":"ENSG00000206853.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":59137372,"end":59137502,"strand":-1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000273566.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":21455236,"end":21455515,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200283.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28972414,"end":28972521,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199585.1","gene_symbol":"RNA5SP119","gene_name":"RNA, 5S ribosomal pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:42917]","synonyms":"RN5S119","biotype":"rRNA","ncbi_id":"100873389","summary":null,"start":211535653,"end":211535769,"strand":1,"description":"RNA, 5S ribosomal pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:42917]"}, {"versioned_ensembl_gene_id":"ENSG00000222449.1","gene_symbol":"RNU6-1140P","gene_name":"RNA, U6 small nuclear 1140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48103]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480068","summary":null,"start":237563165,"end":237563270,"strand":1,"description":"RNA, U6 small nuclear 1140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48103]"}, {"versioned_ensembl_gene_id":"ENSG00000241082.3","gene_symbol":"RN7SL259P","gene_name":"RNA, 7SL, cytoplasmic 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:46275]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480992","summary":null,"start":62935982,"end":62936234,"strand":-1,"description":"RNA, 7SL, cytoplasmic 259, pseudogene [Source:HGNC Symbol;Acc:HGNC:46275]"}, {"versioned_ensembl_gene_id":"ENSG00000284575.1","gene_symbol":"MIR4793","gene_name":"microRNA 4793 [Source:HGNC Symbol;Acc:HGNC:41538]","synonyms":"hsa-mir-4793","biotype":"miRNA","ncbi_id":"100616112","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48644194,"end":48644280,"strand":-1,"description":"microRNA 4793 [Source:HGNC Symbol;Acc:HGNC:41538]"}, {"versioned_ensembl_gene_id":"ENSG00000239856.3","gene_symbol":"RN7SL225P","gene_name":"RNA, 7SL, cytoplasmic 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:46241]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479304","summary":null,"start":86324012,"end":86324309,"strand":-1,"description":"RNA, 7SL, cytoplasmic 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:46241]"}, {"versioned_ensembl_gene_id":"ENSG00000240327.3","gene_symbol":"RN7SL93P","gene_name":"RNA, 7SL, cytoplasmic 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:46109]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480947","summary":null,"start":113976341,"end":113976633,"strand":-1,"description":"RNA, 7SL, cytoplasmic 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:46109]"}, {"versioned_ensembl_gene_id":"ENSG00000222222.1","gene_symbol":"RNU2-17P","gene_name":"RNA, U2 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48510]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480204","summary":null,"start":150236967,"end":150237156,"strand":1,"description":"RNA, U2 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48510]"}, {"versioned_ensembl_gene_id":"ENSG00000206730.1","gene_symbol":"RNU6-468P","gene_name":"RNA, U6 small nuclear 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:47431]","synonyms":null,"biotype":"snRNA","ncbi_id":"106865374","summary":null,"start":17578631,"end":17578739,"strand":1,"description":"RNA, U6 small nuclear 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:47431]"}, {"versioned_ensembl_gene_id":"ENSG00000275067.1","gene_symbol":"MIR6825","gene_name":"microRNA 6825 [Source:HGNC Symbol;Acc:HGNC:50208]","synonyms":"hsa-mir-6825","biotype":"miRNA","ncbi_id":"102466199","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127575266,"end":127575331,"strand":-1,"description":"microRNA 6825 [Source:HGNC Symbol;Acc:HGNC:50208]"}, {"versioned_ensembl_gene_id":"ENSG00000274816.1","gene_symbol":"MIR6772","gene_name":"microRNA 6772 [Source:HGNC Symbol;Acc:HGNC:50064]","synonyms":"hsa-mir-6772","biotype":"miRNA","ncbi_id":"102465463","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57772289,"end":57772352,"strand":-1,"description":"microRNA 6772 [Source:HGNC Symbol;Acc:HGNC:50064]"}, {"versioned_ensembl_gene_id":"ENSG00000266107.1","gene_symbol":"MIR4525","gene_name":"microRNA 4525 [Source:HGNC Symbol;Acc:HGNC:41903]","synonyms":"hsa-mir-4525","biotype":"miRNA","ncbi_id":"100616196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82668233,"end":82668307,"strand":-1,"description":"microRNA 4525 [Source:HGNC Symbol;Acc:HGNC:41903]"}, {"versioned_ensembl_gene_id":"ENSG00000238830.1","gene_symbol":"RNU7-46P","gene_name":"RNA, U7 small nuclear 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:34142]","synonyms":"U7.46","biotype":"snRNA","ncbi_id":"100147833","summary":null,"start":98840675,"end":98840736,"strand":-1,"description":"RNA, U7 small nuclear 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:34142]"}, {"versioned_ensembl_gene_id":"ENSG00000207456.1","gene_symbol":"RNU6-997P","gene_name":"RNA, U6 small nuclear 997, pseudogene [Source:HGNC Symbol;Acc:HGNC:47960]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480007","summary":null,"start":53570374,"end":53570480,"strand":-1,"description":"RNA, U6 small nuclear 997, pseudogene [Source:HGNC Symbol;Acc:HGNC:47960]"}, {"versioned_ensembl_gene_id":"ENSG00000244256.3","gene_symbol":"RN7SL130P","gene_name":"RNA, 7SL, cytoplasmic 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:46146]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479269","summary":null,"start":63655743,"end":63656047,"strand":1,"description":"RNA, 7SL, cytoplasmic 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:46146]"}, {"versioned_ensembl_gene_id":"ENSG00000202206.1","gene_symbol":"RNU6-169P","gene_name":"RNA, U6 small nuclear 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:47132]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481229","summary":null,"start":195514036,"end":195514142,"strand":1,"description":"RNA, U6 small nuclear 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:47132]"}, {"versioned_ensembl_gene_id":"ENSG00000265145.1","gene_symbol":"SNORD53","gene_name":"small nucleolar RNA, C/D box 53 [Source:HGNC Symbol;Acc:HGNC:10203]","synonyms":"U53,SNORD53A,RNU53","biotype":"snoRNA","ncbi_id":"26796","summary":null,"start":28927067,"end":28927144,"strand":1,"description":"small nucleolar RNA, C/D box 53 [Source:HGNC Symbol;Acc:HGNC:10203]"}, {"versioned_ensembl_gene_id":"ENSG00000200331.1","gene_symbol":"RNU6-183P","gene_name":"RNA, U6 small nuclear 183, pseudogene [Source:HGNC Symbol;Acc:HGNC:47146]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481234","summary":null,"start":78314916,"end":78315025,"strand":-1,"description":"RNA, U6 small nuclear 183, pseudogene [Source:HGNC Symbol;Acc:HGNC:47146]"}, {"versioned_ensembl_gene_id":"ENSG00000200711.1","gene_symbol":"RNA5SP28","gene_name":"RNA, 5S ribosomal pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42604]","synonyms":"RN5S28","biotype":"rRNA","ncbi_id":"100873360","summary":null,"start":50812988,"end":50813106,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42604]"}, {"versioned_ensembl_gene_id":"ENSG00000265368.1","gene_symbol":"MIR4476","gene_name":"microRNA 4476 [Source:HGNC Symbol;Acc:HGNC:41793]","synonyms":"hsa-mir-4476","biotype":"miRNA","ncbi_id":"100616456","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36893462,"end":36893531,"strand":-1,"description":"microRNA 4476 [Source:HGNC Symbol;Acc:HGNC:41793]"}, {"versioned_ensembl_gene_id":"ENSG00000215939.3","gene_symbol":"MIR873","gene_name":"microRNA 873 [Source:HGNC Symbol;Acc:HGNC:33663]","synonyms":"MIRN873,hsa-mir-873","biotype":"miRNA","ncbi_id":"100126316","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28888879,"end":28888955,"strand":-1,"description":"microRNA 873 [Source:HGNC Symbol;Acc:HGNC:33663]"}, {"versioned_ensembl_gene_id":"ENSG00000274051.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76721216,"end":76721396,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000212551.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":32081764,"end":32081973,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000250751.1","gene_symbol":"AC015795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49708334,"end":49720060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206804.1","gene_symbol":"RNU6-1293P","gene_name":"RNA, U6 small nuclear 1293, pseudogene [Source:HGNC Symbol;Acc:HGNC:48256]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480130","summary":null,"start":64880369,"end":64880475,"strand":-1,"description":"RNA, U6 small nuclear 1293, pseudogene [Source:HGNC Symbol;Acc:HGNC:48256]"}, {"versioned_ensembl_gene_id":"ENSG00000283506.1","gene_symbol":"MIR7157","gene_name":"microRNA 7157 [Source:HGNC Symbol;Acc:HGNC:50010]","synonyms":"hsa-mir-7157","biotype":"miRNA","ncbi_id":"102465692","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140586626,"end":140586685,"strand":-1,"description":"microRNA 7157 [Source:HGNC Symbol;Acc:HGNC:50010]"}, {"versioned_ensembl_gene_id":"ENSG00000251870.1","gene_symbol":"RNU2-69P","gene_name":"RNA, U2 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:48562]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481656","summary":null,"start":58926197,"end":58926296,"strand":-1,"description":"RNA, U2 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:48562]"}, {"versioned_ensembl_gene_id":"ENSG00000265134.1","gene_symbol":"MIR3190","gene_name":"microRNA 3190 [Source:HGNC Symbol;Acc:HGNC:38190]","synonyms":"hsa-mir-3190","biotype":"miRNA","ncbi_id":"100422899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47226942,"end":47227021,"strand":1,"description":"microRNA 3190 [Source:HGNC Symbol;Acc:HGNC:38190]"}, {"versioned_ensembl_gene_id":"ENSG00000252716.1","gene_symbol":"RN7SKP260","gene_name":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479211","summary":null,"start":206260066,"end":206260214,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]"}, {"versioned_ensembl_gene_id":"ENSG00000199870.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75353885,"end":75353986,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239744.3","gene_symbol":"RN7SL63P","gene_name":"RNA, 7SL, cytoplasmic 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46079]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480939","summary":null,"start":30555601,"end":30555904,"strand":-1,"description":"RNA, 7SL, cytoplasmic 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46079]"}, {"versioned_ensembl_gene_id":"ENSG00000274544.1","gene_symbol":"SNORD28","gene_name":"small nucleolar RNA, C/D box 28 [Source:HGNC Symbol;Acc:HGNC:10150]","synonyms":"U28,SNORD28A,RNU28","biotype":"snoRNA","ncbi_id":"9300","summary":null,"start":62854621,"end":62854695,"strand":-1,"description":"small nucleolar RNA, C/D box 28 [Source:HGNC Symbol;Acc:HGNC:10150]"}, {"versioned_ensembl_gene_id":"ENSG00000275287.5","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":388100,"end":388389,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200146.1","gene_symbol":"RNU6-544P","gene_name":"RNA, U6 small nuclear 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:47507]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481353","summary":null,"start":80527960,"end":80528066,"strand":1,"description":"RNA, U6 small nuclear 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:47507]"}, {"versioned_ensembl_gene_id":"ENSG00000275359.1","gene_symbol":"ST7-AS1_1","gene_name":"ST7 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02179]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116952698,"end":116952813,"strand":1,"description":"ST7 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02179]"}, {"versioned_ensembl_gene_id":"ENSG00000277912.1","gene_symbol":"MIR8089","gene_name":"microRNA 8089 [Source:HGNC Symbol;Acc:HGNC:50196]","synonyms":"hsa-mir-8089","biotype":"miRNA","ncbi_id":"102465882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181043403,"end":181043484,"strand":-1,"description":"microRNA 8089 [Source:HGNC Symbol;Acc:HGNC:50196]"}, {"versioned_ensembl_gene_id":"ENSG00000265699.1","gene_symbol":"MIR548AE2","gene_name":"microRNA 548ae-2 [Source:HGNC Symbol;Acc:HGNC:41831]","synonyms":"hsa-mir-548ae-2","biotype":"miRNA","ncbi_id":"100616339","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58530043,"end":58530109,"strand":-1,"description":"microRNA 548ae-2 [Source:HGNC Symbol;Acc:HGNC:41831]"}, {"versioned_ensembl_gene_id":"ENSG00000264024.2","gene_symbol":"MIR4507","gene_name":"microRNA 4507 [Source:HGNC Symbol;Acc:HGNC:41642]","synonyms":"hsa-mir-4507","biotype":"miRNA","ncbi_id":"100616135","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105858124,"end":105858175,"strand":-1,"description":"microRNA 4507 [Source:HGNC Symbol;Acc:HGNC:41642]"}, {"versioned_ensembl_gene_id":"ENSG00000249881.1","gene_symbol":"AC008696.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":143605628,"end":143828772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252867.1","gene_symbol":"RNU6-909P","gene_name":"RNA, U6 small nuclear 909, pseudogene [Source:HGNC Symbol;Acc:HGNC:47872]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481466","summary":null,"start":28624657,"end":28624763,"strand":1,"description":"RNA, U6 small nuclear 909, pseudogene [Source:HGNC Symbol;Acc:HGNC:47872]"}, {"versioned_ensembl_gene_id":"ENSG00000264602.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30922178,"end":30922269,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222266.1","gene_symbol":"RNU6-757P","gene_name":"RNA, U6 small nuclear 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:47720]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479901","summary":null,"start":134715483,"end":134715582,"strand":1,"description":"RNA, U6 small nuclear 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:47720]"}, {"versioned_ensembl_gene_id":"ENSG00000275881.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62393607,"end":62393880,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266890.1","gene_symbol":"MIR4634","gene_name":"microRNA 4634 [Source:HGNC Symbol;Acc:HGNC:41559]","synonyms":"hsa-mir-4634","biotype":"miRNA","ncbi_id":"100616202","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":174751734,"end":174751787,"strand":1,"description":"microRNA 4634 [Source:HGNC Symbol;Acc:HGNC:41559]"}, {"versioned_ensembl_gene_id":"ENSG00000207207.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85434507,"end":85434619,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263390.1","gene_symbol":"hsa-mir-3119-1","gene_name":"hsa-mir-3119-1 [Source:miRBase;Acc:MI0014134]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":170151378,"end":170151462,"strand":1,"description":"hsa-mir-3119-1 [Source:miRBase;Acc:MI0014134]"}, {"versioned_ensembl_gene_id":"ENSG00000252919.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49592236,"end":49592337,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277217.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129170092,"end":129170238,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000253056.1","gene_symbol":"RNU7-128P","gene_name":"RNA, U7 small nuclear 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:45662]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480819","summary":null,"start":48180328,"end":48180389,"strand":1,"description":"RNA, U7 small nuclear 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:45662]"}, {"versioned_ensembl_gene_id":"ENSG00000277515.1","gene_symbol":"RN7SL495P","gene_name":"RNA, 7SL, cytoplasmic 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:46511]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479404","summary":null,"start":22609141,"end":22609377,"strand":-1,"description":"RNA, 7SL, cytoplasmic 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:46511]"}, {"versioned_ensembl_gene_id":"ENSG00000265013.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29582051,"end":29582134,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000277980.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30825003,"end":30825096,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200090.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47726894,"end":47726992,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199751.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":71491066,"end":71491167,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221081.1","gene_symbol":"MIR320D2","gene_name":"microRNA 320d-2 [Source:HGNC Symbol;Acc:HGNC:35388]","synonyms":"MIRN320D2,hsa-mir-320d-2","biotype":"miRNA","ncbi_id":"100302169","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140926172,"end":140926219,"strand":-1,"description":"microRNA 320d-2 [Source:HGNC Symbol;Acc:HGNC:35388]"}, {"versioned_ensembl_gene_id":"ENSG00000284231.1","gene_symbol":"MIR424","gene_name":"microRNA 424 [Source:HGNC Symbol;Acc:HGNC:31881]","synonyms":"MIRN424,hsa-mir-424","biotype":"miRNA","ncbi_id":"494336","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134546614,"end":134546711,"strand":-1,"description":"microRNA 424 [Source:HGNC Symbol;Acc:HGNC:31881]"}, {"versioned_ensembl_gene_id":"ENSG00000239517.1","gene_symbol":"AC116337.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74931662,"end":74931817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249343.1","gene_symbol":"LINC01333","gene_name":"long intergenic non-protein coding RNA 1333 [Source:HGNC Symbol;Acc:HGNC:50539]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929082","summary":null,"start":74322486,"end":74328297,"strand":1,"description":"long intergenic non-protein coding RNA 1333 [Source:HGNC Symbol;Acc:HGNC:50539]"}, {"versioned_ensembl_gene_id":"ENSG00000280924.1","gene_symbol":"LINC00628","gene_name":"long intergenic non-protein coding RNA 628 [Source:HGNC Symbol;Acc:HGNC:27008]","synonyms":null,"biotype":"lincRNA","ncbi_id":"127841","summary":null,"start":204368431,"end":204369719,"strand":-1,"description":"long intergenic non-protein coding RNA 628 [Source:HGNC Symbol;Acc:HGNC:27008]"}, {"versioned_ensembl_gene_id":"ENSG00000268364.1","gene_symbol":"SMC5-AS1","gene_name":"SMC5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48718]","synonyms":"MAMDC2-AS2","biotype":"antisense_RNA","ncbi_id":"100507299","summary":null,"start":70193997,"end":70258866,"strand":-1,"description":"SMC5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48718]"}, {"versioned_ensembl_gene_id":"ENSG00000165525.17","gene_symbol":"NEMF","gene_name":"nuclear export mediator factor [Source:HGNC Symbol;Acc:HGNC:10663]","synonyms":"SDCCAG1,NY-CO-1,FLJ10051","biotype":"protein_coding","ncbi_id":"9147","summary":"This gene encodes a component of the ribosome quality control complex. The encoded protein facilitates the recognition and ubiquitination of stalled 60S subunits by the ubiquitin ligase listerin. A similar protein in fly functions as a tumor suppressor. [provided by RefSeq, Jul 2016]","start":49782083,"end":49853203,"strand":-1,"description":"nuclear export mediator factor [Source:HGNC Symbol;Acc:HGNC:10663]"}, {"versioned_ensembl_gene_id":"ENSG00000165516.10","gene_symbol":"KLHDC2","gene_name":"kelch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20231]","synonyms":"LCP,HCLP-1","biotype":"protein_coding","ncbi_id":"23588","summary":null,"start":49767608,"end":49786385,"strand":1,"description":"kelch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20231]"}, {"versioned_ensembl_gene_id":"ENSG00000258560.1","gene_symbol":"AL157912.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100052803,"end":100074878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266497.1","gene_symbol":"AC138645.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46503946,"end":46509339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176087.14","gene_symbol":"SLC35A4","gene_name":"solute carrier family 35 member A4 [Source:HGNC Symbol;Acc:HGNC:20753]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113829","summary":null,"start":140564456,"end":140569103,"strand":1,"description":"solute carrier family 35 member A4 [Source:HGNC Symbol;Acc:HGNC:20753]"}, {"versioned_ensembl_gene_id":"ENSG00000113108.19","gene_symbol":"APBB3","gene_name":"amyloid beta precursor protein binding family B member 3 [Source:HGNC Symbol;Acc:HGNC:20708]","synonyms":"FE65L2","biotype":"protein_coding","ncbi_id":"10307","summary":"The protein encoded by this gene is a member of the APBB protein family. It is found in the cytoplasm and binds to the intracellular domain of the Alzheimer's disease beta-amyloid precursor protein (APP) as well as to other APP-like proteins. It is thought that the protein encoded by this gene may modulate the internalization of APP. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":140558268,"end":140564781,"strand":-1,"description":"amyloid beta precursor protein binding family B member 3 [Source:HGNC Symbol;Acc:HGNC:20708]"}, {"versioned_ensembl_gene_id":"ENSG00000271198.1","gene_symbol":"VDAC3P1","gene_name":"voltage dependent anion channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20722]","synonyms":"VDAC3P","biotype":"processed_pseudogene","ncbi_id":"341965","summary":null,"start":99964529,"end":99965378,"strand":1,"description":"voltage dependent anion channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20722]"}, {"versioned_ensembl_gene_id":"ENSG00000267750.5","gene_symbol":"RUNDC3A-AS1","gene_name":"RUNDC3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51344]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926996","summary":null,"start":44299574,"end":44315315,"strand":-1,"description":"RUNDC3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51344]"}, {"versioned_ensembl_gene_id":"ENSG00000162736.15","gene_symbol":"NCSTN","gene_name":"nicastrin [Source:HGNC Symbol;Acc:HGNC:17091]","synonyms":"KIAA0253,APH2","biotype":"protein_coding","ncbi_id":"23385","summary":"This gene encodes a type I transmembrane glycoprotein that is an integral component of the multimeric gamma-secretase complex. The encoded protein cleaves integral membrane proteins, including Notch receptors and beta-amyloid precursor protein, and may be a stabilizing cofactor required for gamma-secretase complex assembly. The cleavage of beta-amyloid precursor protein yields amyloid beta peptide, the main component of the neuritic plaque and the hallmark lesion in the brains of patients with Alzheimer's disease; however, the nature of the encoded protein's role in Alzheimer's disease is not known for certain. Mutations in this gene are associated with familial acne inversa. A pseudogene of this gene is present on chromosome 21. Alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Feb 2014]","start":160343272,"end":160358952,"strand":1,"description":"nicastrin [Source:HGNC Symbol;Acc:HGNC:17091]"}, {"versioned_ensembl_gene_id":"ENSG00000258297.1","gene_symbol":"AP001157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66666036,"end":66668374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182004.12","gene_symbol":"SNRPE","gene_name":"small nuclear ribonucleoprotein polypeptide E [Source:HGNC Symbol;Acc:HGNC:11161]","synonyms":"Sm-E","biotype":"protein_coding","ncbi_id":"6635","summary":"The protein encoded by this gene is a core component of U small nuclear ribonucleoproteins, which are key components of the pre-mRNA processing spliceosome. The encoded protein plays a role in the 3' end processing of histone transcripts. This protein is one of the targets in the autoimmune disease systemic lupus erythematosus, and mutations in this gene have been associated with hypotrichosis. Several pseudogenes of this gene have been identified. [provided by RefSeq, Jun 2016]","start":203861603,"end":203870550,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E [Source:HGNC Symbol;Acc:HGNC:11161]"}, {"versioned_ensembl_gene_id":"ENSG00000229832.1","gene_symbol":"AL360091.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":212357418,"end":212358353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173933.19","gene_symbol":"RBM4","gene_name":"RNA binding motif protein 4 [Source:HGNC Symbol;Acc:HGNC:9901]","synonyms":"ZCCHC21,RBM4A,LARK,ZCRB3A","biotype":"protein_coding","ncbi_id":"5936","summary":null,"start":66638617,"end":66666682,"strand":1,"description":"RNA binding motif protein 4 [Source:HGNC Symbol;Acc:HGNC:9901]"}, {"versioned_ensembl_gene_id":"ENSG00000251556.1","gene_symbol":"AC091887.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146099406,"end":146120412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141522.11","gene_symbol":"ARHGDIA","gene_name":"Rho GDP dissociation inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:678]","synonyms":"RHOGDI,GDIA1","biotype":"protein_coding","ncbi_id":"396","summary":"This gene encodes a protein that plays a key role in the regulation of signaling through Rho GTPases. The encoded protein inhibits the disassociation of Rho family members from GDP (guanine diphosphate), thereby maintaining these factors in an inactive state. Activity of this protein is important in a variety of cellular processes, and expression of this gene may be altered in tumors. Mutations in this gene have been found in individuals with nephrotic syndrome, type 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":81867721,"end":81871406,"strand":-1,"description":"Rho GDP dissociation inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:678]"}, {"versioned_ensembl_gene_id":"ENSG00000248125.1","gene_symbol":"AC008700.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145429868,"end":145451099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119139.17","gene_symbol":"TJP2","gene_name":"tight junction protein 2 [Source:HGNC Symbol;Acc:HGNC:11828]","synonyms":"ZO2,ZO-2,X104,DFNA51","biotype":"protein_coding","ncbi_id":"9414","summary":"This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":69121264,"end":69255208,"strand":1,"description":"tight junction protein 2 [Source:HGNC Symbol;Acc:HGNC:11828]"}, {"versioned_ensembl_gene_id":"ENSG00000258750.2","gene_symbol":"AL358335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48398310,"end":48399375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250692.1","gene_symbol":"AC008667.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139848290,"end":139856389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259117.1","gene_symbol":"AL121576.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47801926,"end":47802201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259129.5","gene_symbol":"LINC00648","gene_name":"long intergenic non-protein coding RNA 648 [Source:HGNC Symbol;Acc:HGNC:44302]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506433","summary":null,"start":47764954,"end":47795092,"strand":-1,"description":"long intergenic non-protein coding RNA 648 [Source:HGNC Symbol;Acc:HGNC:44302]"}, {"versioned_ensembl_gene_id":"ENSG00000162735.18","gene_symbol":"PEX19","gene_name":"peroxisomal biogenesis factor 19 [Source:HGNC Symbol;Acc:HGNC:9713]","synonyms":"PXMP1,PXF,PMPI,PMP1,HK33,D1S2223E","biotype":"protein_coding","ncbi_id":"5824","summary":"This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":160276812,"end":160286348,"strand":-1,"description":"peroxisomal biogenesis factor 19 [Source:HGNC Symbol;Acc:HGNC:9713]"}, {"versioned_ensembl_gene_id":"ENSG00000232002.1","gene_symbol":"LINC01880","gene_name":"long intergenic non-protein coding RNA 1880 [Source:HGNC Symbol;Acc:HGNC:52699]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373979","summary":null,"start":242047695,"end":242084138,"strand":-1,"description":"long intergenic non-protein coding RNA 1880 [Source:HGNC Symbol;Acc:HGNC:52699]"}, {"versioned_ensembl_gene_id":"ENSG00000220537.1","gene_symbol":"AL121977.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82263996,"end":82264974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247828.7","gene_symbol":"TMEM161B-AS1","gene_name":"TMEM161B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43839]","synonyms":"linc-POLR3G-8","biotype":"antisense_RNA","ncbi_id":"100505894","summary":null,"start":88268895,"end":88436685,"strand":1,"description":"TMEM161B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43839]"}, {"versioned_ensembl_gene_id":"ENSG00000214401.4","gene_symbol":"KANSL1-AS1","gene_name":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644246","summary":null,"start":46193576,"end":46196723,"strand":1,"description":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]"}, {"versioned_ensembl_gene_id":"ENSG00000262372.1","gene_symbol":"CR936218.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46035313,"end":46035770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262772.1","gene_symbol":"LINC01977","gene_name":"long intergenic non-protein coding RNA 1977 [Source:HGNC Symbol;Acc:HGNC:52804]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371919","summary":null,"start":79823452,"end":79827704,"strand":1,"description":"long intergenic non-protein coding RNA 1977 [Source:HGNC Symbol;Acc:HGNC:52804]"}, {"versioned_ensembl_gene_id":"ENSG00000259717.1","gene_symbol":"LINC00677","gene_name":"long intergenic non-protein coding RNA 677 [Source:HGNC Symbol;Acc:HGNC:20121]","synonyms":"C14orf74","biotype":"lincRNA","ncbi_id":"105370683","summary":null,"start":103120847,"end":103123007,"strand":-1,"description":"long intergenic non-protein coding RNA 677 [Source:HGNC Symbol;Acc:HGNC:20121]"}, {"versioned_ensembl_gene_id":"ENSG00000273645.2","gene_symbol":"KBTBD11","gene_name":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]","synonyms":"KLHDC7C,KIAA0711","biotype":"protein_coding","ncbi_id":"9920","summary":null,"start":1973878,"end":2006936,"strand":1,"description":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]"}, {"versioned_ensembl_gene_id":"ENSG00000139970.16","gene_symbol":"RTN1","gene_name":"reticulon 1 [Source:HGNC Symbol;Acc:HGNC:10467]","synonyms":"NSP","biotype":"protein_coding","ncbi_id":"6252","summary":"This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. This gene is considered to be a specific marker for neurological diseases and cancer, and is a potential molecular target for therapy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2011]","start":59595976,"end":59870966,"strand":-1,"description":"reticulon 1 [Source:HGNC Symbol;Acc:HGNC:10467]"}, {"versioned_ensembl_gene_id":"ENSG00000225014.1","gene_symbol":"KCTD9P1","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21428]","synonyms":"HsT38306","biotype":"transcribed_processed_pseudogene","ncbi_id":"100422273","summary":null,"start":20111824,"end":20112990,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21428]"}, {"versioned_ensembl_gene_id":"ENSG00000283769.1","gene_symbol":"CR392000.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136263925,"end":136267237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064195.7","gene_symbol":"DLX3","gene_name":"distal-less homeobox 3 [Source:HGNC Symbol;Acc:HGNC:2916]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1747","summary":"Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. [provided by RefSeq, Jul 2008]","start":49990005,"end":49995224,"strand":-1,"description":"distal-less homeobox 3 [Source:HGNC Symbol;Acc:HGNC:2916]"}, {"versioned_ensembl_gene_id":"ENSG00000227455.2","gene_symbol":"AL450345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164827750,"end":164831630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156453.13","gene_symbol":"PCDH1","gene_name":"protocadherin 1 [Source:HGNC Symbol;Acc:HGNC:8655]","synonyms":"pc42","biotype":"protein_coding","ncbi_id":"5097","summary":"This gene belongs to the protocadherin subfamily within the cadherin superfamily. The encoded protein is a membrane protein found at cell-cell boundaries. It is involved in neural cell adhesion, suggesting a possible role in neuronal development. The protein includes an extracelllular region, containing 7 cadherin-like domains, a transmembrane region and a C-terminal cytoplasmic region. Cells expressing the protein showed cell aggregation activity. Alternative splicing occurs in this gene. [provided by RefSeq, Jul 2008]","start":141853111,"end":141879246,"strand":-1,"description":"protocadherin 1 [Source:HGNC Symbol;Acc:HGNC:8655]"}, {"versioned_ensembl_gene_id":"ENSG00000250882.1","gene_symbol":"AC010261.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112173570,"end":112175548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239481.1","gene_symbol":"RPS3AP41","gene_name":"ribosomal protein S3a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271595","summary":null,"start":71669520,"end":71670297,"strand":1,"description":"ribosomal protein S3a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37000]"}, {"versioned_ensembl_gene_id":"ENSG00000254892.1","gene_symbol":"AP003396.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119403963,"end":119404227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254740.2","gene_symbol":"AP003396.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119372706,"end":119381613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108219.14","gene_symbol":"TSPAN14","gene_name":"tetraspanin 14 [Source:HGNC Symbol;Acc:HGNC:23303]","synonyms":"TM4SF14,MGC11352,DC-TM4F2","biotype":"protein_coding","ncbi_id":"81619","summary":null,"start":80454166,"end":80533123,"strand":1,"description":"tetraspanin 14 [Source:HGNC Symbol;Acc:HGNC:23303]"}, {"versioned_ensembl_gene_id":"ENSG00000100767.15","gene_symbol":"PAPLN","gene_name":"papilin, proteoglycan like sulfated glycoprotein [Source:HGNC Symbol;Acc:HGNC:19262]","synonyms":"MGC50452","biotype":"protein_coding","ncbi_id":"89932","summary":null,"start":73237497,"end":73274640,"strand":1,"description":"papilin, proteoglycan like sulfated glycoprotein [Source:HGNC Symbol;Acc:HGNC:19262]"}, {"versioned_ensembl_gene_id":"ENSG00000258944.1","gene_symbol":"AC004846.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73272182,"end":73274081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217195.1","gene_symbol":"AL513475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144706733,"end":144707047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055208.18","gene_symbol":"TAB2","gene_name":"TGF-beta activated kinase 1/MAP3K7 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17075]","synonyms":"MAP3K7IP2,KIAA0733","biotype":"protein_coding","ncbi_id":"23118","summary":"The protein encoded by this gene is an activator of MAP3K7/TAK1, which is required for for the IL-1 induced activation of nuclear factor kappaB and MAPK8/JNK. This protein forms a kinase complex with TRAF6, MAP3K7 and TAB1, and it thus serves as an adaptor that links MAP3K7 and TRAF6. This protein, along with TAB1 and MAP3K7, also participates in the signal transduction induced by TNFSF11/RANKl through the activation of the receptor activator of NF-kappaB (TNFRSF11A/RANK), which may regulate the development and function of osteoclasts. Studies of the related mouse protein indicate that it functions to protect against liver damage caused by chemical stressors. Mutations in this gene cause congenital heart defects, multiple types, 2 (CHTD2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":149218641,"end":149411613,"strand":1,"description":"TGF-beta activated kinase 1/MAP3K7 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17075]"}, {"versioned_ensembl_gene_id":"ENSG00000149150.8","gene_symbol":"SLC43A1","gene_name":"solute carrier family 43 member 1 [Source:HGNC Symbol;Acc:HGNC:9225]","synonyms":"POV1,PB39,R00504","biotype":"protein_coding","ncbi_id":"8501","summary":"SLC43A1 belongs to the system L family of plasma membrane carrier proteins that transports large neutral amino acids (Babu et al., 2003 [PubMed 12930836]).[supplied by OMIM, Mar 2008]","start":57484534,"end":57515786,"strand":-1,"description":"solute carrier family 43 member 1 [Source:HGNC Symbol;Acc:HGNC:9225]"}, {"versioned_ensembl_gene_id":"ENSG00000071246.10","gene_symbol":"VASH1","gene_name":"vasohibin 1 [Source:HGNC Symbol;Acc:HGNC:19964]","synonyms":"KIAA1036","biotype":"protein_coding","ncbi_id":"22846","summary":null,"start":76762189,"end":76783015,"strand":1,"description":"vasohibin 1 [Source:HGNC Symbol;Acc:HGNC:19964]"}, {"versioned_ensembl_gene_id":"ENSG00000258610.1","gene_symbol":"AF111169.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76778952,"end":76782249,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230666.5","gene_symbol":"CEACAM22P","gene_name":"carcinoembryonic antigen related cell adhesion molecule 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38029]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388550","summary":null,"start":44537058,"end":44620821,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38029]"}, {"versioned_ensembl_gene_id":"ENSG00000040933.15","gene_symbol":"INPP4A","gene_name":"inositol polyphosphate-4-phosphatase type I A [Source:HGNC Symbol;Acc:HGNC:6074]","synonyms":"INPP4","biotype":"protein_coding","ncbi_id":"3631","summary":"This gene encodes an Mg++ independent enzyme that hydrolyzes the 4-position phosphate from the inositol ring of phosphatidylinositol 3,4-bisphosphate, inositol 1,3,4-trisphosphate, and inositol 3,4-bisphosphate. Multiple transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Aug 2008]","start":98444854,"end":98594390,"strand":1,"description":"inositol polyphosphate-4-phosphatase type I A [Source:HGNC Symbol;Acc:HGNC:6074]"}, {"versioned_ensembl_gene_id":"ENSG00000250921.1","gene_symbol":"LINC02063","gene_name":"long intergenic non-protein coding RNA 2063 [Source:HGNC Symbol;Acc:HGNC:52908]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374627","summary":null,"start":4135682,"end":4143648,"strand":1,"description":"long intergenic non-protein coding RNA 2063 [Source:HGNC Symbol;Acc:HGNC:52908]"}, {"versioned_ensembl_gene_id":"ENSG00000260763.1","gene_symbol":"AC106799.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4436850,"end":4440259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254417.1","gene_symbol":"ANO1-AS2","gene_name":"ANO1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:33275]","synonyms":"NCRNA00224,C11orf78","biotype":"antisense_RNA","ncbi_id":"100009613","summary":null,"start":70072434,"end":70075433,"strand":-1,"description":"ANO1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:33275]"}, {"versioned_ensembl_gene_id":"ENSG00000228982.1","gene_symbol":"AL627095.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":247085389,"end":247086067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261382.1","gene_symbol":"AC091962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153901459,"end":153903223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135740.16","gene_symbol":"SLC9A5","gene_name":"solute carrier family 9 member A5 [Source:HGNC Symbol;Acc:HGNC:11078]","synonyms":"NHE5","biotype":"protein_coding","ncbi_id":"6553","summary":null,"start":67237683,"end":67272190,"strand":1,"description":"solute carrier family 9 member A5 [Source:HGNC Symbol;Acc:HGNC:11078]"}, {"versioned_ensembl_gene_id":"ENSG00000105605.7","gene_symbol":"CACNG7","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:13626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59284","summary":"The protein encoded by this gene is a type II transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type I TARP and a calcium channel gamma subunit. [provided by RefSeq, Dec 2010]","start":53909335,"end":53943941,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:13626]"}, {"versioned_ensembl_gene_id":"ENSG00000235397.1","gene_symbol":"EPN2-AS1","gene_name":"EPN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40849]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874018","summary":null,"start":19296596,"end":19306261,"strand":-1,"description":"EPN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40849]"}, {"versioned_ensembl_gene_id":"ENSG00000234575.1","gene_symbol":"CTSLP8","gene_name":"cathepsin L pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39084]","synonyms":"CTSL1P8","biotype":"unprocessed_pseudogene","ncbi_id":"1518","summary":null,"start":87844152,"end":87847314,"strand":1,"description":"cathepsin L pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39084]"}, {"versioned_ensembl_gene_id":"ENSG00000260482.3","gene_symbol":"AC008870.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":23670011,"end":23675499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249478.1","gene_symbol":"AC010307.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133243764,"end":133248781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226089.2","gene_symbol":"AL122017.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":81527102,"end":81534915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250409.1","gene_symbol":"AC010608.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133387773,"end":133388549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112297.14","gene_symbol":"CRYBG1","gene_name":"crystallin beta-gamma domain containing 1 [Source:HGNC Symbol;Acc:HGNC:356]","synonyms":"ST4,AIM1","biotype":"protein_coding","ncbi_id":"202","summary":null,"start":106360808,"end":106571978,"strand":1,"description":"crystallin beta-gamma domain containing 1 [Source:HGNC Symbol;Acc:HGNC:356]"}, {"versioned_ensembl_gene_id":"ENSG00000166847.9","gene_symbol":"DCTN5","gene_name":"dynactin subunit 5 [Source:HGNC Symbol;Acc:HGNC:24594]","synonyms":"p25,MGC3248","biotype":"protein_coding","ncbi_id":"84516","summary":"This gene encodes a subunit of dynactin, a component of the cytoplasmic dynein motor machinery involved in minus-end-directed transport. The encoded protein is a component of the pointed-end subcomplex and is thought to bind membranous cargo. A pseudogene of this gene is located on the long arm of chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":23641392,"end":23677455,"strand":1,"description":"dynactin subunit 5 [Source:HGNC Symbol;Acc:HGNC:24594]"}, {"versioned_ensembl_gene_id":"ENSG00000269590.1","gene_symbol":"AC010422.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12664828,"end":12669397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162373.12","gene_symbol":"BEND5","gene_name":"BEN domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25668]","synonyms":"FLJ11588,C1orf165","biotype":"protein_coding","ncbi_id":"79656","summary":null,"start":48727523,"end":48776969,"strand":-1,"description":"BEN domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25668]"}, {"versioned_ensembl_gene_id":"ENSG00000183605.16","gene_symbol":"SFXN4","gene_name":"sideroflexin 4 [Source:HGNC Symbol;Acc:HGNC:16088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119559","summary":"This gene encodes a member of the sideroflexin family. The encoded protein is a transmembrane protein of the inner mitochondrial membrane, and is required for mitochondrial respiratory homeostasis and erythropoiesis. Mutations in this gene are associated with mitochondriopathy and macrocytic anemia. Alternatively spliced transcript variants have been found in this gene. [provided by RefSeq, Jan 2014]","start":119140767,"end":119165667,"strand":-1,"description":"sideroflexin 4 [Source:HGNC Symbol;Acc:HGNC:16088]"}, {"versioned_ensembl_gene_id":"ENSG00000229846.1","gene_symbol":"AC092264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49048316,"end":49187585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281856.1","gene_symbol":"AC106017.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19219143,"end":19222527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204650.14","gene_symbol":"LINC02210","gene_name":"long intergenic non-protein coding RNA 2210 [Source:HGNC Symbol;Acc:HGNC:26327]","synonyms":"CRHR1-IT1,C17orf69,CRHR1-IT1,C17orf69,FLJ25168","biotype":"transcribed_unitary_pseudogene","ncbi_id":"147081","summary":null,"start":45620328,"end":45655156,"strand":1,"description":"long intergenic non-protein coding RNA 2210 [Source:HGNC Symbol;Acc:HGNC:26327]"}, {"versioned_ensembl_gene_id":"ENSG00000263715.7","gene_symbol":"LINC02210-CRHR1","gene_name":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]","synonyms":null,"biotype":"protein_coding","ncbi_id":"104909134","summary":"This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene. [provided by RefSeq, Dec 2016]","start":45620344,"end":45835826,"strand":1,"description":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]"}, {"versioned_ensembl_gene_id":"ENSG00000102595.19","gene_symbol":"UGGT2","gene_name":"UDP-glucose glycoprotein glucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15664]","synonyms":"UGCGL2,MGC87276,MGC150689,MGC117360,HUGT2,FLJ11485,FLJ10873","biotype":"protein_coding","ncbi_id":"55757","summary":"UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009]","start":95801580,"end":96053482,"strand":-1,"description":"UDP-glucose glycoprotein glucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15664]"}, {"versioned_ensembl_gene_id":"ENSG00000265547.1","gene_symbol":"AC217774.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45731703,"end":45732977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185294.6","gene_symbol":"SPPL2C","gene_name":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]","synonyms":"IMP5,IMP5","biotype":"protein_coding","ncbi_id":"162540","summary":null,"start":45844835,"end":45847072,"strand":1,"description":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]"}, {"versioned_ensembl_gene_id":"ENSG00000215796.3","gene_symbol":"AL512637.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247042791,"end":247044021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186280.6","gene_symbol":"KDM4D","gene_name":"lysine demethylase 4D [Source:HGNC Symbol;Acc:HGNC:25498]","synonyms":"JMJD2D,FLJ10251","biotype":"protein_coding","ncbi_id":"55693","summary":null,"start":94973681,"end":94999518,"strand":1,"description":"lysine demethylase 4D [Source:HGNC Symbol;Acc:HGNC:25498]"}, {"versioned_ensembl_gene_id":"ENSG00000105369.9","gene_symbol":"CD79A","gene_name":"CD79a molecule [Source:HGNC Symbol;Acc:HGNC:1698]","synonyms":"MB-1,IGA","biotype":"protein_coding","ncbi_id":"973","summary":"The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":41877120,"end":41881372,"strand":1,"description":"CD79a molecule [Source:HGNC Symbol;Acc:HGNC:1698]"}, {"versioned_ensembl_gene_id":"ENSG00000262870.1","gene_symbol":"CYCSP40","gene_name":"cytochrome c, somatic pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:24414]","synonyms":"HC7,HCP40","biotype":"processed_pseudogene","ncbi_id":"360185","summary":null,"start":77198950,"end":77199543,"strand":-1,"description":"cytochrome c, somatic pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:24414]"}, {"versioned_ensembl_gene_id":"ENSG00000219361.1","gene_symbol":"RPSAP72","gene_name":"ribosomal protein SA pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:51925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075112","summary":null,"start":80470071,"end":80470428,"strand":-1,"description":"ribosomal protein SA pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:51925]"}, {"versioned_ensembl_gene_id":"ENSG00000260645.1","gene_symbol":"AL359715.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80466958,"end":80469080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066739.11","gene_symbol":"ATG2B","gene_name":"autophagy related 2B [Source:HGNC Symbol;Acc:HGNC:20187]","synonyms":"FLJ10242,C14orf103","biotype":"protein_coding","ncbi_id":"55102","summary":"This gene encodes a protein required for autophagy. The encoded protein is involved in autophagosome formation. A germline duplication of a region that includes this gene is associated with predisposition to myeloid malignancies. [provided by RefSeq, Jul 2016]","start":96279202,"end":96363870,"strand":-1,"description":"autophagy related 2B [Source:HGNC Symbol;Acc:HGNC:20187]"}, {"versioned_ensembl_gene_id":"ENSG00000067829.18","gene_symbol":"IDH3G","gene_name":"isocitrate dehydrogenase 3 (NAD(+)) gamma [Source:HGNC Symbol;Acc:HGNC:5386]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3421","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. NAD(+)-dependent isocitrate dehydrogenases catalyze the allosterically regulated rate-limiting step of the tricarboxylic acid cycle. Each isozyme is a heterotetramer that is composed of two alpha subunits, one beta subunit, and one gamma subunit. The protein encoded by this gene is the gamma subunit of one isozyme of NAD(+)-dependent isocitrate dehydrogenase. This gene is a candidate gene for periventricular heterotopia. Several alternatively spliced transcript variants of this gene have been described, but only some of their full length natures have been determined. [provided by RefSeq, Jul 2008]","start":153785766,"end":153794523,"strand":-1,"description":"isocitrate dehydrogenase 3 (NAD(+)) gamma [Source:HGNC Symbol;Acc:HGNC:5386]"}, {"versioned_ensembl_gene_id":"ENSG00000180879.13","gene_symbol":"SSR4","gene_name":"signal sequence receptor subunit 4 [Source:HGNC Symbol;Acc:HGNC:11326]","synonyms":"TRAPD","biotype":"protein_coding","ncbi_id":"6748","summary":"This gene encodes the delta subunit of the translocon-associated protein complex which is involved in translocating proteins across the endoplasmic reticulum membrane. The encoded protein is located in the Xq28 region and is arranged in a compact head-to-head manner with the isocitrate dehydrogenase 3 (NAD+) gamma gene and both genes are driven by a CpG-embedded bidirectional promoter. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]","start":153793516,"end":153798505,"strand":1,"description":"signal sequence receptor subunit 4 [Source:HGNC Symbol;Acc:HGNC:11326]"}, {"versioned_ensembl_gene_id":"ENSG00000271833.1","gene_symbol":"AL445222.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":127366770,"end":127367397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269502.5","gene_symbol":"DMRTC1","gene_name":"DMRT like family C1 [Source:HGNC Symbol;Acc:HGNC:13910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63947","summary":null,"start":72872025,"end":72943814,"strand":-1,"description":"DMRT like family C1 [Source:HGNC Symbol;Acc:HGNC:13910]"}, {"versioned_ensembl_gene_id":"ENSG00000112309.10","gene_symbol":"B3GAT2","gene_name":"beta-1,3-glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:922]","synonyms":"GlcAT-S","biotype":"protein_coding","ncbi_id":"135152","summary":"The product of this gene is a transmembrane protein belonging to the glucuronyltransferase family, and catalyzes the transfer of a beta-1,3 linked glucuronic acid to a terminal galactose in different glycoproteins or glycolipids containing a Gal-beta-1-4GlcNAc or Gal-beta-1-3GlcNAc residue. The encoded protein is involved in the synthesis of the human natural killer-1 (HNK-1) carbohydrate epitope, a sulfated trisaccharide implicated in cellular migration and adhesion in the nervous system. [provided by RefSeq, Jul 2008]","start":70856679,"end":70957038,"strand":-1,"description":"beta-1,3-glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:922]"}, {"versioned_ensembl_gene_id":"ENSG00000258793.1","gene_symbol":"AL355102.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96259411,"end":96268624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120318.15","gene_symbol":"ARAP3","gene_name":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:24097]","synonyms":"FLJ21065,DRAG1,CENTD3","biotype":"protein_coding","ncbi_id":"64411","summary":"This gene encodes a phosphoinositide binding protein containing ARF-GAP, RHO-GAP, RAS-associating, and pleckstrin homology domains. The ARF-GAP and RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton and cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Sep 2015]","start":141653401,"end":141682221,"strand":-1,"description":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:24097]"}, {"versioned_ensembl_gene_id":"ENSG00000258402.1","gene_symbol":"AC016526.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76280943,"end":76310066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267535.1","gene_symbol":"LINC00868","gene_name":"long intergenic non-protein coding RNA 868 [Source:HGNC Symbol;Acc:HGNC:27562]","synonyms":"C17orf52","biotype":"lincRNA","ncbi_id":"283994","summary":null,"start":76850176,"end":76861836,"strand":1,"description":"long intergenic non-protein coding RNA 868 [Source:HGNC Symbol;Acc:HGNC:27562]"}, {"versioned_ensembl_gene_id":"ENSG00000267198.1","gene_symbol":"AC091132.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45545804,"end":45563230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086848.14","gene_symbol":"ALG9","gene_name":"ALG9, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:15672]","synonyms":"DIBD1","biotype":"protein_coding","ncbi_id":"79796","summary":"This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":111782195,"end":111871581,"strand":-1,"description":"ALG9, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:15672]"}, {"versioned_ensembl_gene_id":"ENSG00000237124.1","gene_symbol":"MTND2P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42112]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873222","summary":null,"start":109300186,"end":109301172,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42112]"}, {"versioned_ensembl_gene_id":"ENSG00000279737.1","gene_symbol":"AC112204.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35895689,"end":35896020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262292.2","gene_symbol":"AC007952.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19160789,"end":19162274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283122.1","gene_symbol":"HYMAI","gene_name":"hydatidiform mole associated and imprinted (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:5326]","synonyms":"NCRNA00020","biotype":"non_coding","ncbi_id":"57061","summary":"This gene, which encodes a non-protein coding transcript, exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island, and is expressed only from the paternal allele. It is believed to be one of the causative genes for transient neonatal diabetes mellitus (TNDM), which is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. [provided by RefSeq, Oct 2010]","start":144004916,"end":144008262,"strand":-1,"description":"hydatidiform mole associated and imprinted (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:5326]"}, {"versioned_ensembl_gene_id":"ENSG00000244717.1","gene_symbol":"AC145146.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69469883,"end":69470136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147642.16","gene_symbol":"SYBU","gene_name":"syntabulin [Source:HGNC Symbol;Acc:HGNC:26011]","synonyms":"SNPHL,OCSYN,KIAA1472,GOLSYN,FLJ20366","biotype":"protein_coding","ncbi_id":"55638","summary":"Syntabulin/GOLSYN is part of a kinesin motor-adaptor complex that is critical for the anterograde axonal transport of active zone components and contributes to activity-dependent presynaptic assembly during neuronal development (Cai et al., 2007 [PubMed 17611281]).[supplied by OMIM, Mar 2008]","start":109573978,"end":109691791,"strand":-1,"description":"syntabulin [Source:HGNC Symbol;Acc:HGNC:26011]"}, {"versioned_ensembl_gene_id":"ENSG00000254052.1","gene_symbol":"IGHVIII-67-4","gene_name":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]","synonyms":"IGHV(III)-67-4","biotype":"IG_V_pseudogene","ncbi_id":"28340","summary":null,"start":106695102,"end":106695397,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]"}, {"versioned_ensembl_gene_id":"ENSG00000254036.1","gene_symbol":"IGHVIII-67-2","gene_name":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]","synonyms":"IGHV(III)-67-2","biotype":"IG_V_pseudogene","ncbi_id":"28342","summary":null,"start":106687113,"end":106687200,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]"}, {"versioned_ensembl_gene_id":"ENSG00000228830.1","gene_symbol":"AL160408.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234607008,"end":234609483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253820.1","gene_symbol":"IGHVII-67-1","gene_name":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]","synonyms":"IGHV(II)-67-1","biotype":"IG_V_pseudogene","ncbi_id":"28358","summary":null,"start":106686517,"end":106686562,"strand":-1,"description":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]"}, {"versioned_ensembl_gene_id":"ENSG00000165629.19","gene_symbol":"ATP5C1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:833]","synonyms":"ATP5CL1,ATP5C","biotype":"protein_coding","ncbi_id":"509","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq, Jul 2008]","start":7788129,"end":7807815,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:833]"}, {"versioned_ensembl_gene_id":"ENSG00000123977.9","gene_symbol":"DAW1","gene_name":"dynein assembly factor with WD repeats 1 [Source:HGNC Symbol;Acc:HGNC:26383]","synonyms":"WDR69,ODA16,FLJ25955","biotype":"protein_coding","ncbi_id":"164781","summary":null,"start":227871054,"end":227924344,"strand":1,"description":"dynein assembly factor with WD repeats 1 [Source:HGNC Symbol;Acc:HGNC:26383]"}, {"versioned_ensembl_gene_id":"ENSG00000149577.15","gene_symbol":"SIDT2","gene_name":"SID1 transmembrane family member 2 [Source:HGNC Symbol;Acc:HGNC:24272]","synonyms":"CGI-40","biotype":"protein_coding","ncbi_id":"51092","summary":null,"start":117178733,"end":117197445,"strand":1,"description":"SID1 transmembrane family member 2 [Source:HGNC Symbol;Acc:HGNC:24272]"}, {"versioned_ensembl_gene_id":"ENSG00000214255.5","gene_symbol":"AC091305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70430231,"end":70431125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232249.1","gene_symbol":"AC152007.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153355733,"end":153355956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197561.6","gene_symbol":"ELANE","gene_name":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]","synonyms":"ELA2,NE,HNE,HLE","biotype":"protein_coding","ncbi_id":"1991","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode structurally similar proteins. The encoded preproprotein is proteolytically processed to generate the active protease. Following activation, this protease hydrolyzes proteins within specialized neutrophil lysosomes, called azurophil granules, as well as proteins of the extracellular matrix. The enzyme may play a role in degenerative and inflammatory diseases through proteolysis of collagen-IV and elastin. This protein also degrades the outer membrane protein A (OmpA) of E. coli as well as the virulence factors of such bacteria as Shigella, Salmonella and Yersinia. Mutations in this gene are associated with cyclic neutropenia and severe congenital neutropenia (SCN). This gene is present in a gene cluster on chromosome 19. [provided by RefSeq, Jan 2016]","start":851014,"end":856247,"strand":1,"description":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]"}, {"versioned_ensembl_gene_id":"ENSG00000166189.7","gene_symbol":"HPS6","gene_name":"HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 [Source:HGNC Symbol;Acc:HGNC:18817]","synonyms":"FLJ22501,BLOC2S3","biotype":"protein_coding","ncbi_id":"79803","summary":"This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]","start":102065390,"end":102068038,"strand":1,"description":"HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 [Source:HGNC Symbol;Acc:HGNC:18817]"}, {"versioned_ensembl_gene_id":"ENSG00000225110.2","gene_symbol":"PNMA6F","gene_name":"paraneoplastic Ma antigen family member 6F [Source:HGNC Symbol;Acc:HGNC:53119]","synonyms":"PNMA6BL","biotype":"protein_coding","ncbi_id":"105373377","summary":null,"start":153317681,"end":153321822,"strand":-1,"description":"paraneoplastic Ma antigen family member 6F [Source:HGNC Symbol;Acc:HGNC:53119]"}, {"versioned_ensembl_gene_id":"ENSG00000249348.1","gene_symbol":"UGDH-AS1","gene_name":"UGDH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40601]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885776","summary":null,"start":39528019,"end":39594707,"strand":1,"description":"UGDH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40601]"}, {"versioned_ensembl_gene_id":"ENSG00000235686.1","gene_symbol":"PPIAP20","gene_name":"peptidylprolyl isomerase A pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100500737","summary":null,"start":12508129,"end":12508263,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38037]"}, {"versioned_ensembl_gene_id":"ENSG00000269693.1","gene_symbol":"AC010422.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12525720,"end":12580975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188831.4","gene_symbol":"DPPA3P2","gene_name":"developmental pluripotency associated 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20417]","synonyms":"STELLAR","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400206","summary":null,"start":36371165,"end":36372383,"strand":1,"description":"developmental pluripotency associated 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20417]"}, {"versioned_ensembl_gene_id":"ENSG00000185009.12","gene_symbol":"AP3M1","gene_name":"adaptor related protein complex 3 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26985","summary":"The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane, and it may directly function in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":74120255,"end":74151063,"strand":-1,"description":"adaptor related protein complex 3 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:569]"}, {"versioned_ensembl_gene_id":"ENSG00000225761.1","gene_symbol":"AL596247.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74005137,"end":74027915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172893.15","gene_symbol":"DHCR7","gene_name":"7-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2860]","synonyms":"SLOS","biotype":"protein_coding","ncbi_id":"1717","summary":"This gene encodes an enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic reticulum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS); a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by cognitive disability, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Aug 2009]","start":71428193,"end":71452868,"strand":-1,"description":"7-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2860]"}, {"versioned_ensembl_gene_id":"ENSG00000252767.1","gene_symbol":"RNU6-250P","gene_name":"RNA, U6 small nuclear 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:47213]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479678","summary":null,"start":40407853,"end":40407955,"strand":1,"description":"RNA, U6 small nuclear 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:47213]"}, {"versioned_ensembl_gene_id":"ENSG00000200391.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43863893,"end":43864005,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221340.1","gene_symbol":"RNU6ATAC18P","gene_name":"RNA, U6atac small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46917]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479551","summary":null,"start":12569972,"end":12570072,"strand":-1,"description":"RNA, U6atac small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46917]"}, {"versioned_ensembl_gene_id":"ENSG00000255114.1","gene_symbol":"AP003392.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119044188,"end":119045493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106665.15","gene_symbol":"CLIP2","gene_name":"CAP-Gly domain containing linker protein 2 [Source:HGNC Symbol;Acc:HGNC:2586]","synonyms":"CYLN2,CLIP-115,CLIP,WSCR4,WSCR3,WBSCR4,WBSCR3,KIAA0291","biotype":"protein_coding","ncbi_id":"7461","summary":"The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":74289475,"end":74405943,"strand":1,"description":"CAP-Gly domain containing linker protein 2 [Source:HGNC Symbol;Acc:HGNC:2586]"}, {"versioned_ensembl_gene_id":"ENSG00000077585.13","gene_symbol":"GPR137B","gene_name":"G protein-coupled receptor 137B [Source:HGNC Symbol;Acc:HGNC:11862]","synonyms":"TM7SF1","biotype":"protein_coding","ncbi_id":"7107","summary":null,"start":236142505,"end":236221865,"strand":1,"description":"G protein-coupled receptor 137B [Source:HGNC Symbol;Acc:HGNC:11862]"}, {"versioned_ensembl_gene_id":"ENSG00000263394.1","gene_symbol":"AC007952.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19091069,"end":19091825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159917.15","gene_symbol":"ZNF235","gene_name":"zinc finger protein 235 [Source:HGNC Symbol;Acc:HGNC:12866]","synonyms":"ZNF270,ZFP93,HZF6,ANF270","biotype":"protein_coding","ncbi_id":"9310","summary":"This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein is a member of the Kruppel family of zinc finger proteins, and contains Kruppel-associated box (KRAB) A and B domains and 15 tandemly arrayed C2H2-type zinc fingers. It is an ortholog of the mouse Zfp93 protein. This gene is located in a cluster of zinc finger genes on 19q13.2. [provided by RefSeq, Jul 2008]","start":44228729,"end":44305046,"strand":-1,"description":"zinc finger protein 235 [Source:HGNC Symbol;Acc:HGNC:12866]"}, {"versioned_ensembl_gene_id":"ENSG00000270679.1","gene_symbol":"AC138473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44290081,"end":44290911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225236.1","gene_symbol":"AP000936.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117117794,"end":117119181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239486.1","gene_symbol":"AC091390.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102380465,"end":102382737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276832.1","gene_symbol":"AL354718.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41341000,"end":41342041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198883.11","gene_symbol":"PNMA5","gene_name":"paraneoplastic Ma antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:18743]","synonyms":"KIAA1934","biotype":"protein_coding","ncbi_id":"114824","summary":"This gene encodes a member of the paraneoplastic Ma antigen protein family. These proteins have been implicated in the development of paraneoplastic disorders resulting from an immune response directed against them. Paraneoplastic disorders are the result of an abnormal immune response to a tumor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2011]","start":152988824,"end":152994127,"strand":-1,"description":"paraneoplastic Ma antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:18743]"}, {"versioned_ensembl_gene_id":"ENSG00000149557.12","gene_symbol":"FEZ1","gene_name":"fasciculation and elongation protein zeta 1 [Source:HGNC Symbol;Acc:HGNC:3659]","synonyms":"UNC-76","biotype":"protein_coding","ncbi_id":"9638","summary":"This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal bundling and elongation within axon bundles. Expression of this gene in C. elegans unc-76 mutants can restore to the mutants partial locomotion and axonal fasciculation, suggesting that it also functions in axonal outgrowth. The N-terminal half of the gene product is highly acidic. Alternatively spliced transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]","start":125445745,"end":125496317,"strand":-1,"description":"fasciculation and elongation protein zeta 1 [Source:HGNC Symbol;Acc:HGNC:3659]"}, {"versioned_ensembl_gene_id":"ENSG00000233011.1","gene_symbol":"SLC9A3P1","gene_name":"solute carrier family 9 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11074]","synonyms":"NHE3P,SLC9A3P4,SLC9A3P","biotype":"processed_pseudogene","ncbi_id":"6551","summary":null,"start":50150603,"end":50152287,"strand":1,"description":"solute carrier family 9 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11074]"}, {"versioned_ensembl_gene_id":"ENSG00000176894.9","gene_symbol":"PXMP2","gene_name":"peroxisomal membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:9716]","synonyms":"PMP22","biotype":"protein_coding","ncbi_id":"5827","summary":null,"start":132687606,"end":132704991,"strand":1,"description":"peroxisomal membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:9716]"}, {"versioned_ensembl_gene_id":"ENSG00000283464.1","gene_symbol":"AC244452.4","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106481424,"end":106481706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275765.5","gene_symbol":"AC091982.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151770242,"end":151771508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253921.1","gene_symbol":"AC091982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151753992,"end":151767247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242042.1","gene_symbol":"LINC01743","gene_name":"long intergenic non-protein coding RNA 1743 [Source:HGNC Symbol;Acc:HGNC:52531]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255654","summary":null,"start":246516039,"end":246524287,"strand":-1,"description":"long intergenic non-protein coding RNA 1743 [Source:HGNC Symbol;Acc:HGNC:52531]"}, {"versioned_ensembl_gene_id":"ENSG00000198700.9","gene_symbol":"IPO9","gene_name":"importin 9 [Source:HGNC Symbol;Acc:HGNC:19425]","synonyms":"Imp9,FLJ10402","biotype":"protein_coding","ncbi_id":"55705","summary":null,"start":201829141,"end":201884294,"strand":1,"description":"importin 9 [Source:HGNC Symbol;Acc:HGNC:19425]"}, {"versioned_ensembl_gene_id":"ENSG00000268423.4","gene_symbol":"AC093503.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46547056,"end":46600861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271043.2","gene_symbol":"MTRNR2L2","gene_name":"MT-RNR2-like 2 [Source:HGNC Symbol;Acc:HGNC:37156]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462981","summary":null,"start":80650000,"end":80650086,"strand":-1,"description":"MT-RNR2-like 2 [Source:HGNC Symbol;Acc:HGNC:37156]"}, {"versioned_ensembl_gene_id":"ENSG00000251396.6","gene_symbol":"LINC01301","gene_name":"long intergenic non-protein coding RNA 1301 [Source:HGNC Symbol;Acc:HGNC:50464]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505532","summary":null,"start":60384588,"end":60516795,"strand":-1,"description":"long intergenic non-protein coding RNA 1301 [Source:HGNC Symbol;Acc:HGNC:50464]"}, {"versioned_ensembl_gene_id":"ENSG00000214215.3","gene_symbol":"C12orf74","gene_name":"chromosome 12 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27887]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338809","summary":null,"start":92702843,"end":92708549,"strand":1,"description":"chromosome 12 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27887]"}, {"versioned_ensembl_gene_id":"ENSG00000258262.1","gene_symbol":"AC063949.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92530460,"end":92531324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049541.10","gene_symbol":"RFC2","gene_name":"replication factor C subunit 2 [Source:HGNC Symbol;Acc:HGNC:9970]","synonyms":"RFC40,A1","biotype":"protein_coding","ncbi_id":"5982","summary":"This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013]","start":74231499,"end":74254458,"strand":-1,"description":"replication factor C subunit 2 [Source:HGNC Symbol;Acc:HGNC:9970]"}, {"versioned_ensembl_gene_id":"ENSG00000279665.1","gene_symbol":"AC012100.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50742702,"end":50743276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259773.1","gene_symbol":"AC012100.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50746709,"end":50749829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250433.1","gene_symbol":"CLSTN2-AS1","gene_name":"CLSTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49095]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927808","summary":null,"start":140505611,"end":140508789,"strand":-1,"description":"CLSTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49095]"}, {"versioned_ensembl_gene_id":"ENSG00000147383.10","gene_symbol":"NSDHL","gene_name":"NAD(P) dependent steroid dehydrogenase-like [Source:HGNC Symbol;Acc:HGNC:13398]","synonyms":"XAP104,SDR31E1,H105e3","biotype":"protein_coding","ncbi_id":"50814","summary":"The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]","start":152830967,"end":152869729,"strand":1,"description":"NAD(P) dependent steroid dehydrogenase-like [Source:HGNC Symbol;Acc:HGNC:13398]"}, {"versioned_ensembl_gene_id":"ENSG00000226773.1","gene_symbol":"AL663109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92203148,"end":92203991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278474.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4a,CD158K,cl-5,nkat4b,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54880532,"end":54897308,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000231810.1","gene_symbol":"RPL36AP35","gene_name":"ribosomal protein L36a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35639]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271610","summary":null,"start":108821697,"end":108822004,"strand":1,"description":"ribosomal protein L36a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35639]"}, {"versioned_ensembl_gene_id":"ENSG00000229052.2","gene_symbol":"AL449283.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":92930696,"end":92934098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253158.1","gene_symbol":"IGKV3-31","gene_name":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28910","summary":null,"start":89252211,"end":89252736,"strand":-1,"description":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]"}, {"versioned_ensembl_gene_id":"ENSG00000230546.1","gene_symbol":"AL445193.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58084419,"end":58084559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271584.2","gene_symbol":"LINC02550","gene_name":"long intergenic non-protein coding RNA 2550 [Source:HGNC Symbol;Acc:HGNC:53585]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369490","summary":null,"start":111091932,"end":111179641,"strand":-1,"description":"long intergenic non-protein coding RNA 2550 [Source:HGNC Symbol;Acc:HGNC:53585]"}, {"versioned_ensembl_gene_id":"ENSG00000271390.1","gene_symbol":"AP003973.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111089870,"end":111090368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277852.1","gene_symbol":"AC244255.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89203509,"end":89203906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211907.1","gene_symbol":"IGHD1-26","gene_name":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]","synonyms":"IGHD126","biotype":"IG_D_gene","ncbi_id":"28506","summary":null,"start":105881034,"end":105881053,"strand":-1,"description":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]"}, {"versioned_ensembl_gene_id":"ENSG00000242472.1","gene_symbol":"IGHJ5","gene_name":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28476","summary":null,"start":105863814,"end":105863862,"strand":-1,"description":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]"}, {"versioned_ensembl_gene_id":"ENSG00000237111.1","gene_symbol":"IGHJ3P","gene_name":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]","synonyms":"Jpsi3","biotype":"IG_J_pseudogene","ncbi_id":"28478","summary":null,"start":105863416,"end":105863465,"strand":-1,"description":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]"}, {"versioned_ensembl_gene_id":"ENSG00000130653.15","gene_symbol":"PNPLA7","gene_name":"patatin like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:24768]","synonyms":"RP11-48C7.2,NTEL1,NTE-R1,FLJ44279,FLJ43070,FLJ31318,C9orf111","biotype":"protein_coding","ncbi_id":"375775","summary":"Human patatin-like phospholipases, such as PNPLA7, have been implicated in regulation of adipocyte differentiation and have been induced by metabolic stimuli (Wilson et al., 2006 [PubMed 16799181]).[supplied by OMIM, Jun 2008]","start":137459953,"end":137550534,"strand":-1,"description":"patatin like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:24768]"}, {"versioned_ensembl_gene_id":"ENSG00000211900.2","gene_symbol":"IGHJ6","gene_name":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28475","summary":null,"start":105863198,"end":105863258,"strand":-1,"description":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]"}, {"versioned_ensembl_gene_id":"ENSG00000249497.1","gene_symbol":"LINC02075","gene_name":"long intergenic non-protein coding RNA 2075 [Source:HGNC Symbol;Acc:HGNC:52921]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927207","summary":null,"start":49457861,"end":49461749,"strand":-1,"description":"long intergenic non-protein coding RNA 2075 [Source:HGNC Symbol;Acc:HGNC:52921]"}, {"versioned_ensembl_gene_id":"ENSG00000250186.3","gene_symbol":"AC091180.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49404081,"end":49405197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237210.1","gene_symbol":"AC073324.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55244247,"end":55245681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256797.1","gene_symbol":"KLRF2","gene_name":"killer cell lectin like receptor F2 [Source:HGNC Symbol;Acc:HGNC:37646]","synonyms":"NKp65","biotype":"protein_coding","ncbi_id":"100431172","summary":null,"start":9881489,"end":9895833,"strand":1,"description":"killer cell lectin like receptor F2 [Source:HGNC Symbol;Acc:HGNC:37646]"}, {"versioned_ensembl_gene_id":"ENSG00000248966.1","gene_symbol":"BCLAF1P1","gene_name":"BCL2 associated transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728366","summary":null,"start":110948029,"end":110950780,"strand":-1,"description":"BCL2 associated transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51329]"}, {"versioned_ensembl_gene_id":"ENSG00000237189.1","gene_symbol":"AL138900.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157287703,"end":157288053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274363.1","gene_symbol":"AC087742.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4267691,"end":4268430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219736.1","gene_symbol":"AL356473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74849077,"end":74850484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254221.2","gene_symbol":"PCDHGB1","gene_name":"protocadherin gamma subfamily B, 1 [Source:HGNC Symbol;Acc:HGNC:8708]","synonyms":"PCDH-GAMMA-B1","biotype":"protein_coding","ncbi_id":"56104","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141350102,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 1 [Source:HGNC Symbol;Acc:HGNC:8708]"}, {"versioned_ensembl_gene_id":"ENSG00000199899.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113156763,"end":113156861,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252391.1","gene_symbol":"RNU6-638P","gene_name":"RNA, U6 small nuclear 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:47601]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481383","summary":null,"start":78696694,"end":78696797,"strand":-1,"description":"RNA, U6 small nuclear 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:47601]"}, {"versioned_ensembl_gene_id":"ENSG00000273701.1","gene_symbol":"PART1_1","gene_name":"Prostate androgen-regulated transcript 1 conserved region 1 [Source:RFAM;Acc:RF02159]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":60487713,"end":60487929,"strand":1,"description":"Prostate androgen-regulated transcript 1 conserved region 1 [Source:RFAM;Acc:RF02159]"}, {"versioned_ensembl_gene_id":"ENSG00000223078.1","gene_symbol":"RNU2-55P","gene_name":"RNA, U2 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48548]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481961","summary":null,"start":23281736,"end":23281909,"strand":-1,"description":"RNA, U2 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48548]"}, {"versioned_ensembl_gene_id":"ENSG00000274017.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49196784,"end":49197062,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000197406.7","gene_symbol":"DIO3","gene_name":"iodothyronine deiodinase 3 [Source:HGNC Symbol;Acc:HGNC:2885]","synonyms":"TXDI3","biotype":"protein_coding","ncbi_id":"1735","summary":"The protein encoded by this intronless gene belongs to the iodothyronine deiodinase family. It catalyzes the inactivation of thyroid hormone by inner ring deiodination of the prohormone thyroxine (T4) and the bioactive hormone 3,3',5-triiodothyronine (T3) to inactive metabolites, 3,3',5'-triiodothyronine (RT3) and 3,3'-diiodothyronine (T2), respectively. This enzyme is highly expressed in pregnant uterus, placenta, fetal and neonatal tissues, and thought to prevent premature exposure of developing fetal tissues to adult levels of thyroid hormones. It regulates circulating fetal thyroid hormone concentrations, and thus plays a critical role in mammalian development. Knockout mice lacking this gene exhibit abnormalities related to development and reproduction, and increased activity of this enzyme in infants with hemangiomas causes severe hypothyroidism. This protein is a selenoprotein, containing the rare selenocysteine (Sec) amino acid at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. [provided by RefSeq, May 2016]","start":101561351,"end":101563452,"strand":1,"description":"iodothyronine deiodinase 3 [Source:HGNC Symbol;Acc:HGNC:2885]"}, {"versioned_ensembl_gene_id":"ENSG00000261868.1","gene_symbol":"MFSD1P1","gene_name":"major facilitator superfamily domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100313532","summary":null,"start":4301372,"end":4302698,"strand":1,"description":"major facilitator superfamily domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50625]"}, {"versioned_ensembl_gene_id":"ENSG00000132388.12","gene_symbol":"UBE2G1","gene_name":"ubiquitin conjugating enzyme E2 G1 [Source:HGNC Symbol;Acc:HGNC:12482]","synonyms":"UBE2G,UBC7","biotype":"protein_coding","ncbi_id":"7326","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family and catalyzes the covalent attachment of ubiquitin to other proteins. The protein may be involved in degradation of muscle-specific proteins. [provided by RefSeq, Jul 2008]","start":4269259,"end":4366628,"strand":-1,"description":"ubiquitin conjugating enzyme E2 G1 [Source:HGNC Symbol;Acc:HGNC:12482]"}, {"versioned_ensembl_gene_id":"ENSG00000258919.1","gene_symbol":"AL049836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101628984,"end":101632530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232482.2","gene_symbol":"AL357134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23410832,"end":23412146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258512.1","gene_symbol":"LINC00239","gene_name":"long intergenic non-protein coding RNA 239 [Source:HGNC Symbol;Acc:HGNC:20119]","synonyms":"NCRNA00239,C14orf72","biotype":"lincRNA","ncbi_id":"145200","summary":null,"start":101730437,"end":101732522,"strand":1,"description":"long intergenic non-protein coding RNA 239 [Source:HGNC Symbol;Acc:HGNC:20119]"}, {"versioned_ensembl_gene_id":"ENSG00000254157.1","gene_symbol":"IGKV2-18","gene_name":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28926","summary":null,"start":89128724,"end":89129483,"strand":-1,"description":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]"}, {"versioned_ensembl_gene_id":"ENSG00000258404.1","gene_symbol":"LINC02320","gene_name":"long intergenic non-protein coding RNA 2320 [Source:HGNC Symbol;Acc:HGNC:53239]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370676","summary":null,"start":101634454,"end":101731108,"strand":-1,"description":"long intergenic non-protein coding RNA 2320 [Source:HGNC Symbol;Acc:HGNC:53239]"}, {"versioned_ensembl_gene_id":"ENSG00000204219.9","gene_symbol":"TCEA3","gene_name":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]","synonyms":"TFIIS.H","biotype":"protein_coding","ncbi_id":"6920","summary":null,"start":23381061,"end":23424740,"strand":-1,"description":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]"}, {"versioned_ensembl_gene_id":"ENSG00000241494.1","gene_symbol":"AL355032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101677943,"end":101678380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223353.2","gene_symbol":"AL589763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":245123471,"end":245124450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167085.11","gene_symbol":"PHB","gene_name":"prohibitin [Source:HGNC Symbol;Acc:HGNC:8912]","synonyms":"PHB1","biotype":"protein_coding","ncbi_id":"5245","summary":"This gene is evolutionarily conserved, and its product is proposed to play a role in human cellular senescence and tumor suppression. Antiproliferative activity is reported to be localized to the 3' UTR, which is proposed to function as a trans-acting regulatory RNA. Several pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":49404049,"end":49414905,"strand":-1,"description":"prohibitin [Source:HGNC Symbol;Acc:HGNC:8912]"}, {"versioned_ensembl_gene_id":"ENSG00000136099.13","gene_symbol":"PCDH8","gene_name":"protocadherin 8 [Source:HGNC Symbol;Acc:HGNC:8660]","synonyms":"ARCADLIN,PAPC","biotype":"protein_coding","ncbi_id":"5100","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The gene encodes an integral membrane protein that is thought to function in cell adhesion in a CNS-specific manner. Unlike classical cadherins, which are generally encoded by 15-17 exons, this gene includes only 3 exons. Notable is the large first exon encoding the extracellular region, including 6 cadherin domains and a transmembrane region. Alternative splicing yields isoforms with unique cytoplasmic tails. [provided by RefSeq, Jul 2008]","start":52842889,"end":52848641,"strand":-1,"description":"protocadherin 8 [Source:HGNC Symbol;Acc:HGNC:8660]"}, {"versioned_ensembl_gene_id":"ENSG00000253026.1","gene_symbol":"RNU6-464P","gene_name":"RNA, U6 small nuclear 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:47427]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479771","summary":null,"start":53153795,"end":53153898,"strand":-1,"description":"RNA, U6 small nuclear 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:47427]"}, {"versioned_ensembl_gene_id":"ENSG00000252010.1","gene_symbol":"SCARNA5","gene_name":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]","synonyms":"U87","biotype":"scaRNA","ncbi_id":"677775","summary":null,"start":233275727,"end":233276002,"strand":1,"description":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]"}, {"versioned_ensembl_gene_id":"ENSG00000252894.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130914340,"end":130914452,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201208.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113178423,"end":113178519,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223298.1","gene_symbol":"RNY3P8","gene_name":"RNA, Ro-associated Y3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42492]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106478985","summary":null,"start":95310830,"end":95310955,"strand":-1,"description":"RNA, Ro-associated Y3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42492]"}, {"versioned_ensembl_gene_id":"ENSG00000266151.1","gene_symbol":"MIR3646","gene_name":"microRNA 3646 [Source:HGNC Symbol;Acc:HGNC:38935]","synonyms":"hsa-mir-3646","biotype":"miRNA","ncbi_id":"100500813","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44408120,"end":44408203,"strand":1,"description":"microRNA 3646 [Source:HGNC Symbol;Acc:HGNC:38935]"}, {"versioned_ensembl_gene_id":"ENSG00000201218.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7102573,"end":7102681,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252042.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75145670,"end":75145762,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278794.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1101007,"end":1101273,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000263816.1","gene_symbol":"MIR548AW","gene_name":"microRNA 548aw [Source:HGNC Symbol;Acc:HGNC:43454]","synonyms":"hsa-mir-548aw","biotype":"miRNA","ncbi_id":"100846992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132945707,"end":132945771,"strand":1,"description":"microRNA 548aw [Source:HGNC Symbol;Acc:HGNC:43454]"}, {"versioned_ensembl_gene_id":"ENSG00000263558.2","gene_symbol":"RN7SL716P","gene_name":"RNA, 7SL, cytoplasmic 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:46732]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479484","summary":null,"start":59059226,"end":59059493,"strand":1,"description":"RNA, 7SL, cytoplasmic 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:46732]"}, {"versioned_ensembl_gene_id":"ENSG00000274632.1","gene_symbol":"RN7SL719P","gene_name":"RNA, 7SL, cytoplasmic 719, pseudogene [Source:HGNC Symbol;Acc:HGNC:46735]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481119","summary":null,"start":28703554,"end":28703790,"strand":-1,"description":"RNA, 7SL, cytoplasmic 719, pseudogene [Source:HGNC Symbol;Acc:HGNC:46735]"}, {"versioned_ensembl_gene_id":"ENSG00000266150.1","gene_symbol":"MIR4711","gene_name":"microRNA 4711 [Source:HGNC Symbol;Acc:HGNC:41847]","synonyms":"hsa-mir-4711","biotype":"miRNA","ncbi_id":"100616409","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59733227,"end":59733296,"strand":-1,"description":"microRNA 4711 [Source:HGNC Symbol;Acc:HGNC:41847]"}, {"versioned_ensembl_gene_id":"ENSG00000207608.3","gene_symbol":"MIR127","gene_name":"microRNA 127 [Source:HGNC Symbol;Acc:HGNC:31509]","synonyms":"MIRN127,hsa-mir-127","biotype":"miRNA","ncbi_id":"406914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100882979,"end":100883075,"strand":1,"description":"microRNA 127 [Source:HGNC Symbol;Acc:HGNC:31509]"}, {"versioned_ensembl_gene_id":"ENSG00000275625.1","gene_symbol":"FTX_4","gene_name":"FTX transcript, XIST regulator conserved region 4 [Source:RFAM;Acc:RF02123]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74281703,"end":74281849,"strand":1,"description":"FTX transcript, XIST regulator conserved region 4 [Source:RFAM;Acc:RF02123]"}, {"versioned_ensembl_gene_id":"ENSG00000283475.1","gene_symbol":"MIR1244-4","gene_name":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504734","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12111952,"end":12112036,"strand":1,"description":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]"}, {"versioned_ensembl_gene_id":"ENSG00000212264.1","gene_symbol":"SNORD65C","gene_name":"small nucleolar RNA, C/D box 65C [Source:HGNC Symbol;Acc:HGNC:52232]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616981","summary":null,"start":23396446,"end":23396516,"strand":1,"description":"small nucleolar RNA, C/D box 65C [Source:HGNC Symbol;Acc:HGNC:52232]"}, {"versioned_ensembl_gene_id":"ENSG00000201809.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":73764279,"end":73764413,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000278483.1","gene_symbol":"MIR8087","gene_name":"microRNA 8087 [Source:HGNC Symbol;Acc:HGNC:50059]","synonyms":"hsa-mir-8087","biotype":"miRNA","ncbi_id":"102465881","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27514970,"end":27515047,"strand":-1,"description":"microRNA 8087 [Source:HGNC Symbol;Acc:HGNC:50059]"}, {"versioned_ensembl_gene_id":"ENSG00000244391.3","gene_symbol":"RN7SL330P","gene_name":"RNA, 7SL, cytoplasmic 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:46346]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481013","summary":null,"start":94361220,"end":94361526,"strand":1,"description":"RNA, 7SL, cytoplasmic 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:46346]"}, {"versioned_ensembl_gene_id":"ENSG00000222832.1","gene_symbol":"RNA5SP120","gene_name":"RNA, 5S ribosomal pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:42918]","synonyms":"RN5S120","biotype":"rRNA","ncbi_id":"100873390","summary":null,"start":216793489,"end":216793600,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:42918]"}, {"versioned_ensembl_gene_id":"ENSG00000252368.1","gene_symbol":"RNA5SP43","gene_name":"RNA, 5S ribosomal pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:42819]","synonyms":"RN5S43","biotype":"rRNA","ncbi_id":"100873282","summary":null,"start":37264677,"end":37264786,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:42819]"}, {"versioned_ensembl_gene_id":"ENSG00000275656.1","gene_symbol":"RFPL3-AS1_1","gene_name":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32188400,"end":32188487,"strand":-1,"description":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]"}, {"versioned_ensembl_gene_id":"ENSG00000266782.1","gene_symbol":"MIR3663","gene_name":"microRNA 3663 [Source:HGNC Symbol;Acc:HGNC:38958]","synonyms":"hsa-mir-3663","biotype":"miRNA","ncbi_id":"100500893","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":117167678,"end":117167774,"strand":-1,"description":"microRNA 3663 [Source:HGNC Symbol;Acc:HGNC:38958]"}, {"versioned_ensembl_gene_id":"ENSG00000273981.1","gene_symbol":"RN7SL106P","gene_name":"RNA, 7SL, cytoplasmic 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:46122]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479261","summary":null,"start":23165897,"end":23166186,"strand":1,"description":"RNA, 7SL, cytoplasmic 106, pseudogene [Source:HGNC Symbol;Acc:HGNC:46122]"}, {"versioned_ensembl_gene_id":"ENSG00000222281.1","gene_symbol":"RN7SKP111","gene_name":"RNA, 7SK small nuclear pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:45835]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479144","summary":null,"start":11818821,"end":11819091,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:45835]"}, {"versioned_ensembl_gene_id":"ENSG00000283938.1","gene_symbol":"MIR3917","gene_name":"microRNA 3917 [Source:HGNC Symbol;Acc:HGNC:38911]","synonyms":"hsa-mir-3917","biotype":"miRNA","ncbi_id":"100500808","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25906362,"end":25906454,"strand":-1,"description":"microRNA 3917 [Source:HGNC Symbol;Acc:HGNC:38911]"}, {"versioned_ensembl_gene_id":"ENSG00000266477.2","gene_symbol":"RN7SL616P","gene_name":"RNA, 7SL, cytoplasmic 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:46632]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481090","summary":null,"start":69478997,"end":69479265,"strand":-1,"description":"RNA, 7SL, cytoplasmic 616, pseudogene [Source:HGNC Symbol;Acc:HGNC:46632]"}, {"versioned_ensembl_gene_id":"ENSG00000241413.3","gene_symbol":"RN7SL441P","gene_name":"RNA, 7SL, cytoplasmic 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:46457]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479383","summary":null,"start":109866214,"end":109866509,"strand":-1,"description":"RNA, 7SL, cytoplasmic 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:46457]"}, {"versioned_ensembl_gene_id":"ENSG00000222224.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28927243,"end":28927340,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206719.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":113950886,"end":113950998,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252401.1","gene_symbol":"RNU4ATAC6P","gene_name":"RNA, U4atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46892]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479540","summary":null,"start":28652630,"end":28652755,"strand":1,"description":"RNA, U4atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46892]"}, {"versioned_ensembl_gene_id":"ENSG00000201613.1","gene_symbol":"RNU6-200P","gene_name":"RNA, U6 small nuclear 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:47163]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479655","summary":null,"start":126590287,"end":126590393,"strand":-1,"description":"RNA, U6 small nuclear 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:47163]"}, {"versioned_ensembl_gene_id":"ENSG00000265894.2","gene_symbol":"RN7SL357P","gene_name":"RNA, 7SL, cytoplasmic 357, pseudogene [Source:HGNC Symbol;Acc:HGNC:46373]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481021","summary":null,"start":56805834,"end":56806131,"strand":1,"description":"RNA, 7SL, cytoplasmic 357, pseudogene [Source:HGNC Symbol;Acc:HGNC:46373]"}, {"versioned_ensembl_gene_id":"ENSG00000264423.2","gene_symbol":"RN7SL718P","gene_name":"RNA, 7SL, cytoplasmic 718, pseudogene [Source:HGNC Symbol;Acc:HGNC:46734]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479485","summary":null,"start":41190927,"end":41191229,"strand":-1,"description":"RNA, 7SL, cytoplasmic 718, pseudogene [Source:HGNC Symbol;Acc:HGNC:46734]"}, {"versioned_ensembl_gene_id":"ENSG00000277474.1","gene_symbol":"MIR6894","gene_name":"microRNA 6894 [Source:HGNC Symbol;Acc:HGNC:49938]","synonyms":"hsa-mir-6894","biotype":"miRNA","ncbi_id":"102466759","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53198889,"end":53198945,"strand":-1,"description":"microRNA 6894 [Source:HGNC Symbol;Acc:HGNC:49938]"}, {"versioned_ensembl_gene_id":"ENSG00000272412.2","gene_symbol":"RN7SL778P","gene_name":"RNA, 7SL, cytoplasmic 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:46794]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479504","summary":null,"start":130310180,"end":130310476,"strand":1,"description":"RNA, 7SL, cytoplasmic 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:46794]"}, {"versioned_ensembl_gene_id":"ENSG00000207291.1","gene_symbol":"RNU6-30P","gene_name":"RNA, U6 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:34274]","synonyms":"RNU6-30","biotype":"snRNA","ncbi_id":"100873747","summary":null,"start":101634006,"end":101634112,"strand":-1,"description":"RNA, U6 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:34274]"}, {"versioned_ensembl_gene_id":"ENSG00000208033.1","gene_symbol":"MIR609","gene_name":"microRNA 609 [Source:HGNC Symbol;Acc:HGNC:32865]","synonyms":"MIRN609,hsa-mir-609","biotype":"miRNA","ncbi_id":"693194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104218789,"end":104218883,"strand":-1,"description":"microRNA 609 [Source:HGNC Symbol;Acc:HGNC:32865]"}, {"versioned_ensembl_gene_id":"ENSG00000201407.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":24133186,"end":24133317,"strand":1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000274428.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":146409903,"end":146410062,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000201339.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93967926,"end":93968020,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263989.2","gene_symbol":"RN7SL615P","gene_name":"RNA, 7SL, cytoplasmic 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:46631]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479446","summary":null,"start":41290280,"end":41290577,"strand":-1,"description":"RNA, 7SL, cytoplasmic 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:46631]"}, {"versioned_ensembl_gene_id":"ENSG00000200033.1","gene_symbol":"RNU6-403P","gene_name":"RNA, U6 small nuclear 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:47366]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480578","summary":null,"start":221837334,"end":221837437,"strand":-1,"description":"RNA, U6 small nuclear 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:47366]"}, {"versioned_ensembl_gene_id":"ENSG00000264833.1","gene_symbol":"RN7SL468P","gene_name":"RNA, 7SL, cytoplasmic 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:46484]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481050","summary":null,"start":119169822,"end":119170115,"strand":1,"description":"RNA, 7SL, cytoplasmic 468, pseudogene [Source:HGNC Symbol;Acc:HGNC:46484]"}, {"versioned_ensembl_gene_id":"ENSG00000200629.1","gene_symbol":"RNY1P11","gene_name":"RNA, Ro-associated Y1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50874]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481710","summary":null,"start":129164849,"end":129164961,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:50874]"}, {"versioned_ensembl_gene_id":"ENSG00000276168.1","gene_symbol":"RN7SL1","gene_name":"RNA, 7SL, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:10038]","synonyms":"7SL,7L1a,RNSRP1,RN7SL","biotype":"misc_RNA","ncbi_id":"6029","summary":"The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL1, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]","start":49586580,"end":49586878,"strand":1,"description":"RNA, 7SL, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:10038]"}, {"versioned_ensembl_gene_id":"ENSG00000206862.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":118569405,"end":118569515,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200485.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33196547,"end":33196637,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200906.1","gene_symbol":"RNU6-854P","gene_name":"RNA, U6 small nuclear 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{"versioned_ensembl_gene_id":"ENSG00000222581.1","gene_symbol":"RNU2-47P","gene_name":"RNA, U2 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:48540]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480672","summary":null,"start":12300266,"end":12300451,"strand":-1,"description":"RNA, U2 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:48540]"}, {"versioned_ensembl_gene_id":"ENSG00000202150.1","gene_symbol":"RNU6-407P","gene_name":"RNA, U6 small nuclear 407, pseudogene [Source:HGNC Symbol;Acc:HGNC:47370]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479745","summary":null,"start":35030317,"end":35030420,"strand":-1,"description":"RNA, U6 small nuclear 407, pseudogene [Source:HGNC Symbol;Acc:HGNC:47370]"}, {"versioned_ensembl_gene_id":"ENSG00000243437.3","gene_symbol":"RN7SL370P","gene_name":"RNA, 7SL, cytoplasmic 370, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207088.1","gene_symbol":"SNORA7B","gene_name":"small nucleolar RNA, H/ACA box 7B [Source:HGNC Symbol;Acc:HGNC:32593]","synonyms":"ACA7B","biotype":"snoRNA","ncbi_id":"677797","summary":null,"start":129397210,"end":129397348,"strand":-1,"description":"small nucleolar RNA, H/ACA box 7B [Source:HGNC Symbol;Acc:HGNC:32593]"}, {"versioned_ensembl_gene_id":"ENSG00000273532.1","gene_symbol":"H19_1","gene_name":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51722,"end":51792,"strand":1,"description":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]"}, {"versioned_ensembl_gene_id":"ENSG00000252416.1","gene_symbol":"RNU6-885P","gene_name":"RNA, U6 small nuclear 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:47848]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481458","summary":null,"start":42832447,"end":42832550,"strand":-1,"description":"RNA, U6 small nuclear 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:47848]"}, {"versioned_ensembl_gene_id":"ENSG00000200153.1","gene_symbol":"RNU6-23P","gene_name":"RNA, U6 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:34267]","synonyms":"RNU6-23","biotype":"snRNA","ncbi_id":"100873755","summary":null,"start":70445293,"end":70445399,"strand":-1,"description":"RNA, U6 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:34267]"}, {"versioned_ensembl_gene_id":"ENSG00000239958.3","gene_symbol":"RN7SL51P","gene_name":"RNA, 7SL, cytoplasmic 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46067]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480936","summary":null,"start":62262387,"end":62262671,"strand":-1,"description":"RNA, 7SL, cytoplasmic 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46067]"}, {"versioned_ensembl_gene_id":"ENSG00000202410.1","gene_symbol":"Y_RNA","gene_name":"Y RNA 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{"versioned_ensembl_gene_id":"ENSG00000201821.1","gene_symbol":"RNU4-9P","gene_name":"RNA, U4 small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42507]","synonyms":null,"biotype":"snRNA","ncbi_id":"100862675","summary":null,"start":21038529,"end":21038667,"strand":-1,"description":"RNA, U4 small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42507]"}, {"versioned_ensembl_gene_id":"ENSG00000277582.1","gene_symbol":"RN7SL428P","gene_name":"RNA, 7SL, cytoplasmic 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:46444]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479379","summary":null,"start":85210053,"end":85210299,"strand":-1,"description":"RNA, 7SL, cytoplasmic 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:46444]"}, {"versioned_ensembl_gene_id":"ENSG00000199476.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48288587,"end":48288694,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206763.1","gene_symbol":"RNU6-10P","gene_name":"RNA, U6 small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34254]","synonyms":"RNU6-10","biotype":"snRNA","ncbi_id":"100873745","summary":null,"start":92701708,"end":92701814,"strand":-1,"description":"RNA, U6 small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34254]"}, {"versioned_ensembl_gene_id":"ENSG00000207871.2","gene_symbol":"MIR513B","gene_name":"microRNA 513b [Source:HGNC Symbol;Acc:HGNC:33935]","synonyms":"MIRN513B,hsa-mir-513b","biotype":"miRNA","ncbi_id":"100313822","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147199044,"end":147199127,"strand":-1,"description":"microRNA 513b [Source:HGNC Symbol;Acc:HGNC:33935]"}, {"versioned_ensembl_gene_id":"ENSG00000251874.1","gene_symbol":"RNU6-615P","gene_name":"RNA, U6 small nuclear 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:47578]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480595","summary":null,"start":83003412,"end":83003517,"strand":1,"description":"RNA, U6 small nuclear 615, pseudogene [Source:HGNC Symbol;Acc:HGNC:47578]"}, {"versioned_ensembl_gene_id":"ENSG00000201800.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":125516979,"end":125517086,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276158.2","gene_symbol":"MIR1264","gene_name":"microRNA 1264 [Source:HGNC Symbol;Acc:HGNC:35246]","synonyms":"hsa-mir-1264,MIRN1264","biotype":"miRNA","ncbi_id":"100302251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114652655,"end":114652723,"strand":1,"description":"microRNA 1264 [Source:HGNC Symbol;Acc:HGNC:35246]"}, {"versioned_ensembl_gene_id":"ENSG00000251886.1","gene_symbol":"RNU6-120P","gene_name":"RNA, U6 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:47083]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479619","summary":null,"start":21120404,"end":21120506,"strand":-1,"description":"RNA, U6 small nuclear 120, pseudogene [Source:HGNC Symbol;Acc:HGNC:47083]"}, {"versioned_ensembl_gene_id":"ENSG00000207290.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128371099,"end":128371212,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199523.1","gene_symbol":"RNA5SP226","gene_name":"RNA, 5S ribosomal pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:43126]","synonyms":"RN5S226","biotype":"rRNA","ncbi_id":"106479000","summary":null,"start":165409562,"end":165409676,"strand":1,"description":"RNA, 5S ribosomal pseudogene 226 [Source:HGNC Symbol;Acc:HGNC:43126]"}, {"versioned_ensembl_gene_id":"ENSG00000201142.1","gene_symbol":"RNVU1-8","gene_name":"RNA, variant U1 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:48315]","synonyms":"vU1.8,RNU1-145","biotype":"snRNA","ncbi_id":"101447996","summary":null,"start":147079746,"end":147079870,"strand":1,"description":"RNA, variant U1 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:48315]"}, {"versioned_ensembl_gene_id":"ENSG00000283461.1","gene_symbol":"hsa-mir-550a-2","gene_name":"hsa-mir-550a-2 [Source:miRBase;Acc:MI0003601]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":32732981,"end":32733077,"strand":-1,"description":"hsa-mir-550a-2 [Source:miRBase;Acc:MI0003601]"}, {"versioned_ensembl_gene_id":"ENSG00000207203.1","gene_symbol":"RNU6-71P","gene_name":"RNA, U6 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:42561]","synonyms":"RNU6-71","biotype":"snRNA","ncbi_id":"100873774","summary":null,"start":36267168,"end":36267274,"strand":1,"description":"RNA, U6 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:42561]"}, {"versioned_ensembl_gene_id":"ENSG00000266776.1","gene_symbol":"MIR4646","gene_name":"microRNA 4646 [Source:HGNC Symbol;Acc:HGNC:41543]","synonyms":"hsa-mir-4646","biotype":"miRNA","ncbi_id":"100616230","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31701029,"end":31701091,"strand":-1,"description":"microRNA 4646 [Source:HGNC Symbol;Acc:HGNC:41543]"}, {"versioned_ensembl_gene_id":"ENSG00000212247.1","gene_symbol":"RNU6-278P","gene_name":"RNA, U6 small nuclear 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:47241]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481767","summary":null,"start":13973316,"end":13973424,"strand":-1,"description":"RNA, U6 small nuclear 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:47241]"}, {"versioned_ensembl_gene_id":"ENSG00000206600.1","gene_symbol":"RNU6-25P","gene_name":"RNA, U6 small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:34251]","synonyms":"RNU6-25","biotype":"snRNA","ncbi_id":"106480704","summary":null,"start":195214787,"end":195214893,"strand":1,"description":"RNA, U6 small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:34251]"}, {"versioned_ensembl_gene_id":"ENSG00000252169.1","gene_symbol":"RNA5SP200","gene_name":"RNA, 5S ribosomal pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:43100]","synonyms":"RN5S200","biotype":"rRNA","ncbi_id":"100873461","summary":null,"start":173292517,"end":173292619,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:43100]"}, {"versioned_ensembl_gene_id":"ENSG00000263981.1","gene_symbol":"MIR5705","gene_name":"microRNA 5705 [Source:HGNC Symbol;Acc:HGNC:43504]","synonyms":"hsa-mir-5705","biotype":"miRNA","ncbi_id":"100847027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87300495,"end":87300583,"strand":-1,"description":"microRNA 5705 [Source:HGNC Symbol;Acc:HGNC:43504]"}, {"versioned_ensembl_gene_id":"ENSG00000199466.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":124766196,"end":124766297,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265648.2","gene_symbol":"RN7SL279P","gene_name":"RNA, 7SL, cytoplasmic 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:46295]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480998","summary":null,"start":70276069,"end":70276352,"strand":1,"description":"RNA, 7SL, cytoplasmic 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:46295]"}, {"versioned_ensembl_gene_id":"ENSG00000207434.1","gene_symbol":"RNU6-1072P","gene_name":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480037","summary":null,"start":12922554,"end":12922660,"strand":1,"description":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]"}, {"versioned_ensembl_gene_id":"ENSG00000239932.3","gene_symbol":"RN7SL606P","gene_name":"RNA, 7SL, cytoplasmic 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:46622]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479443","summary":null,"start":60696313,"end":60696605,"strand":1,"description":"RNA, 7SL, cytoplasmic 606, pseudogene [Source:HGNC Symbol;Acc:HGNC:46622]"}, {"versioned_ensembl_gene_id":"ENSG00000222778.1","gene_symbol":"RNA5SP144","gene_name":"RNA, 5S ribosomal pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:43044]","synonyms":"RN5S144","biotype":"rRNA","ncbi_id":"100873411","summary":null,"start":144186905,"end":144187020,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:43044]"}, {"versioned_ensembl_gene_id":"ENSG00000280751.1","gene_symbol":"AKR7A2P1","gene_name":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]","synonyms":"AFARP1","biotype":"processed_pseudogene","ncbi_id":"246182","summary":null,"start":112923423,"end":112924337,"strand":1,"description":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]"}, {"versioned_ensembl_gene_id":"ENSG00000266754.2","gene_symbol":"RN7SL524P","gene_name":"RNA, 7SL, cytoplasmic 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:46540]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481066","summary":null,"start":103974515,"end":103974814,"strand":-1,"description":"RNA, 7SL, cytoplasmic 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:46540]"}, {"versioned_ensembl_gene_id":"ENSG00000202019.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31230071,"end":31230172,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201289.1","gene_symbol":"RN7SKP76","gene_name":"RNA, 7SK small nuclear pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:45800]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481808","summary":null,"start":61743154,"end":61743476,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:45800]"}, {"versioned_ensembl_gene_id":"ENSG00000251914.1","gene_symbol":"RNU7-200P","gene_name":"RNA, U7 small nuclear 200 pseudogene [Source:HGNC Symbol;Acc:HGNC:45734]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480835","summary":null,"start":20841241,"end":20841302,"strand":1,"description":"RNA, U7 small nuclear 200 pseudogene [Source:HGNC Symbol;Acc:HGNC:45734]"}, {"versioned_ensembl_gene_id":"ENSG00000224278.1","gene_symbol":"AL592447.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188242139,"end":188242678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275652.1","gene_symbol":"MIR6796","gene_name":"microRNA 6796 [Source:HGNC Symbol;Acc:HGNC:50186]","synonyms":"hsa-mir-6796","biotype":"miRNA","ncbi_id":"102465477","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40369846,"end":40369907,"strand":1,"description":"microRNA 6796 [Source:HGNC Symbol;Acc:HGNC:50186]"}, {"versioned_ensembl_gene_id":"ENSG00000252225.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36440880,"end":36440970,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252569.1","gene_symbol":"RNU6-1153P","gene_name":"RNA, U6 small nuclear 1153, pseudogene [Source:HGNC Symbol;Acc:HGNC:48116]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480643","summary":null,"start":53443228,"end":53443332,"strand":-1,"description":"RNA, U6 small nuclear 1153, pseudogene [Source:HGNC Symbol;Acc:HGNC:48116]"}, {"versioned_ensembl_gene_id":"ENSG00000212464.1","gene_symbol":"SNORA12","gene_name":"small nucleolar RNA, H/ACA box 12 [Source:HGNC Symbol;Acc:HGNC:32600]","synonyms":"U108","biotype":"snoRNA","ncbi_id":"677800","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":100237156,"end":100237302,"strand":-1,"description":"small nucleolar RNA, H/ACA box 12 [Source:HGNC Symbol;Acc:HGNC:32600]"}, {"versioned_ensembl_gene_id":"ENSG00000199168.3","gene_symbol":"MIR374A","gene_name":"microRNA 374a [Source:HGNC Symbol;Acc:HGNC:31788]","synonyms":"MIRN374A,MIRN374,hsa-mir-374a,hsa-mir-374","biotype":"miRNA","ncbi_id":"442919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74287286,"end":74287357,"strand":-1,"description":"microRNA 374a [Source:HGNC Symbol;Acc:HGNC:31788]"}, {"versioned_ensembl_gene_id":"ENSG00000284190.1","gene_symbol":"MIR21","gene_name":"microRNA 21 [Source:HGNC Symbol;Acc:HGNC:31586]","synonyms":"MIRN21,MIR-21,hsa-mir-21","biotype":"miRNA","ncbi_id":"406991","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59841266,"end":59841337,"strand":1,"description":"microRNA 21 [Source:HGNC Symbol;Acc:HGNC:31586]"}, {"versioned_ensembl_gene_id":"ENSG00000199949.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86275429,"end":86275523,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278526.1","gene_symbol":"ST7-OT3_2","gene_name":"ST7 overlapping transcript 3 conserved region 2 [Source:RFAM;Acc:RF02184]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117190133,"end":117190269,"strand":1,"description":"ST7 overlapping transcript 3 conserved region 2 [Source:RFAM;Acc:RF02184]"}, {"versioned_ensembl_gene_id":"ENSG00000283770.1","gene_symbol":"MIR6849","gene_name":"microRNA 6849 [Source:HGNC Symbol;Acc:HGNC:49991]","synonyms":"hsa-mir-6849","biotype":"miRNA","ncbi_id":"102466749","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144400277,"end":144400345,"strand":-1,"description":"microRNA 6849 [Source:HGNC Symbol;Acc:HGNC:49991]"}, {"versioned_ensembl_gene_id":"ENSG00000222509.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":170783167,"end":170783271,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211997.1","gene_symbol":"MIR708","gene_name":"microRNA 708 [Source:HGNC Symbol;Acc:HGNC:33654]","synonyms":"MIRN708,hsa-mir-708","biotype":"miRNA","ncbi_id":"100126333","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79402022,"end":79402109,"strand":-1,"description":"microRNA 708 [Source:HGNC Symbol;Acc:HGNC:33654]"}, {"versioned_ensembl_gene_id":"ENSG00000200029.1","gene_symbol":"RNU6-642P","gene_name":"RNA, U6 small nuclear 642, pseudogene [Source:HGNC Symbol;Acc:HGNC:47605]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481384","summary":null,"start":218916184,"end":218916287,"strand":-1,"description":"RNA, U6 small nuclear 642, pseudogene [Source:HGNC Symbol;Acc:HGNC:47605]"}, {"versioned_ensembl_gene_id":"ENSG00000207467.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48809911,"end":48810016,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221611.1","gene_symbol":"SNORD88","gene_name":"Small nucleolar RNA SNORD88 [Source:RFAM;Acc:RF00604]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":12972053,"end":12972143,"strand":1,"description":"Small nucleolar RNA SNORD88 [Source:RFAM;Acc:RF00604]"}, {"versioned_ensembl_gene_id":"ENSG00000269859.1","gene_symbol":"AC008735.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55475983,"end":55476482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284047.1","gene_symbol":"MIR6836","gene_name":"microRNA 6836 [Source:HGNC Symbol;Acc:HGNC:50067]","synonyms":"hsa-mir-6836","biotype":"miRNA","ncbi_id":"102465503","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2257515,"end":2257577,"strand":-1,"description":"microRNA 6836 [Source:HGNC Symbol;Acc:HGNC:50067]"}, {"versioned_ensembl_gene_id":"ENSG00000252489.1","gene_symbol":"RNU6-197P","gene_name":"RNA, U6 small nuclear 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:47160]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479654","summary":null,"start":56288485,"end":56288584,"strand":-1,"description":"RNA, U6 small nuclear 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:47160]"}, {"versioned_ensembl_gene_id":"ENSG00000200164.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69191123,"end":69191223,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265806.1","gene_symbol":"MIR4292","gene_name":"microRNA 4292 [Source:HGNC Symbol;Acc:HGNC:38348]","synonyms":"hsa-mir-4292","biotype":"miRNA","ncbi_id":"100422860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136830957,"end":136831023,"strand":1,"description":"microRNA 4292 [Source:HGNC Symbol;Acc:HGNC:38348]"}, {"versioned_ensembl_gene_id":"ENSG00000221563.1","gene_symbol":"MIR1269A","gene_name":"microRNA 1269a [Source:HGNC Symbol;Acc:HGNC:35337]","synonyms":"MIRN1269,MIR1269,hsa-mir-1269","biotype":"miRNA","ncbi_id":"100302177","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66276824,"end":66276928,"strand":1,"description":"microRNA 1269a [Source:HGNC Symbol;Acc:HGNC:35337]"}, {"versioned_ensembl_gene_id":"ENSG00000263670.1","gene_symbol":"MIR4457","gene_name":"microRNA 4457 [Source:HGNC Symbol;Acc:HGNC:41554]","synonyms":"hsa-mir-4457","biotype":"miRNA","ncbi_id":"100616235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1309310,"end":1309377,"strand":-1,"description":"microRNA 4457 [Source:HGNC Symbol;Acc:HGNC:41554]"}, {"versioned_ensembl_gene_id":"ENSG00000266690.1","gene_symbol":"MIR4274","gene_name":"microRNA 4274 [Source:HGNC Symbol;Acc:HGNC:38194]","synonyms":"hsa-mir-4274","biotype":"miRNA","ncbi_id":"100422826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7460028,"end":7460118,"strand":1,"description":"microRNA 4274 [Source:HGNC Symbol;Acc:HGNC:38194]"}, {"versioned_ensembl_gene_id":"ENSG00000252639.1","gene_symbol":"RNU2-24P","gene_name":"RNA, U2 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:48517]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480207","summary":null,"start":27193358,"end":27193500,"strand":-1,"description":"RNA, U2 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:48517]"}, {"versioned_ensembl_gene_id":"ENSG00000265328.1","gene_symbol":"MIR548AB","gene_name":"microRNA 548ab [Source:HGNC Symbol;Acc:HGNC:41825]","synonyms":"hsa-mir-548ab","biotype":"miRNA","ncbi_id":"100616336","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103524033,"end":103524116,"strand":-1,"description":"microRNA 548ab [Source:HGNC Symbol;Acc:HGNC:41825]"}, {"versioned_ensembl_gene_id":"ENSG00000212214.1","gene_symbol":"SNORA48B","gene_name":"small nucleolar RNA, H/ACA box 48B [Source:HGNC Symbol;Acc:HGNC:52207]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616969","summary":null,"start":3532117,"end":3532251,"strand":-1,"description":"small nucleolar RNA, H/ACA box 48B [Source:HGNC Symbol;Acc:HGNC:52207]"}, {"versioned_ensembl_gene_id":"ENSG00000279214.1","gene_symbol":"AL109659.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48262230,"end":48263179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198987.1","gene_symbol":"MIR16-2","gene_name":"microRNA 16-2 [Source:HGNC Symbol;Acc:HGNC:31546]","synonyms":"MIRN16-2,hsa-mir-16-2","biotype":"miRNA","ncbi_id":"406951","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160404745,"end":160404825,"strand":1,"description":"microRNA 16-2 [Source:HGNC Symbol;Acc:HGNC:31546]"}, {"versioned_ensembl_gene_id":"ENSG00000265253.1","gene_symbol":"MIR4446","gene_name":"microRNA 4446 [Source:HGNC Symbol;Acc:HGNC:41700]","synonyms":"hsa-mir-4446","biotype":"miRNA","ncbi_id":"100616476","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113594876,"end":113594942,"strand":1,"description":"microRNA 4446 [Source:HGNC Symbol;Acc:HGNC:41700]"}, {"versioned_ensembl_gene_id":"ENSG00000264013.1","gene_symbol":"MIR3938","gene_name":"microRNA 3938 [Source:HGNC Symbol;Acc:HGNC:38972]","synonyms":"hsa-mir-3938","biotype":"miRNA","ncbi_id":"100500875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55852492,"end":55852594,"strand":-1,"description":"microRNA 3938 [Source:HGNC Symbol;Acc:HGNC:38972]"}, {"versioned_ensembl_gene_id":"ENSG00000284364.1","gene_symbol":"MIR6824","gene_name":"microRNA 6824 [Source:HGNC Symbol;Acc:HGNC:49946]","synonyms":"hsa-mir-6824","biotype":"miRNA","ncbi_id":"102465495","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48633636,"end":48633698,"strand":-1,"description":"microRNA 6824 [Source:HGNC Symbol;Acc:HGNC:49946]"}, {"versioned_ensembl_gene_id":"ENSG00000284092.1","gene_symbol":"MIR5703","gene_name":"microRNA 5703 [Source:HGNC Symbol;Acc:HGNC:43475]","synonyms":"hsa-mir-5703","biotype":"miRNA","ncbi_id":"100847081","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":227472132,"end":227472187,"strand":1,"description":"microRNA 5703 [Source:HGNC Symbol;Acc:HGNC:43475]"}, {"versioned_ensembl_gene_id":"ENSG00000264139.1","gene_symbol":"MIR3667","gene_name":"microRNA 3667 [Source:HGNC Symbol;Acc:HGNC:38990]","synonyms":"hsa-mir-3667","biotype":"miRNA","ncbi_id":"100500882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49543393,"end":49543466,"strand":-1,"description":"microRNA 3667 [Source:HGNC Symbol;Acc:HGNC:38990]"}, {"versioned_ensembl_gene_id":"ENSG00000274385.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":30713240,"end":30713346,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200963.1","gene_symbol":"RNU6-289P","gene_name":"RNA, U6 small nuclear 289, pseudogene [Source:HGNC Symbol;Acc:HGNC:47252]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479695","summary":null,"start":111331412,"end":111331518,"strand":1,"description":"RNA, U6 small nuclear 289, pseudogene [Source:HGNC Symbol;Acc:HGNC:47252]"}, {"versioned_ensembl_gene_id":"ENSG00000252035.1","gene_symbol":"RNU6-397P","gene_name":"RNA, U6 small nuclear 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:47360]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479741","summary":null,"start":14487776,"end":14487879,"strand":-1,"description":"RNA, U6 small nuclear 397, pseudogene [Source:HGNC Symbol;Acc:HGNC:47360]"}, {"versioned_ensembl_gene_id":"ENSG00000252568.1","gene_symbol":"RNU7-28P","gene_name":"RNA, U7 small nuclear 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:34124]","synonyms":"U7.28","biotype":"snRNA","ncbi_id":"100147815","summary":null,"start":9843815,"end":9843876,"strand":-1,"description":"RNA, U7 small nuclear 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:34124]"}, {"versioned_ensembl_gene_id":"ENSG00000266705.1","gene_symbol":"MIR4437","gene_name":"microRNA 4437 [Source:HGNC Symbol;Acc:HGNC:41715]","synonyms":"hsa-mir-4437","biotype":"miRNA","ncbi_id":"100616213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181305593,"end":181305652,"strand":-1,"description":"microRNA 4437 [Source:HGNC Symbol;Acc:HGNC:41715]"}, {"versioned_ensembl_gene_id":"ENSG00000242614.3","gene_symbol":"RN7SL164P","gene_name":"RNA, 7SL, cytoplasmic 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:46180]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480965","summary":null,"start":96169545,"end":96169847,"strand":1,"description":"RNA, 7SL, cytoplasmic 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:46180]"}, {"versioned_ensembl_gene_id":"ENSG00000252136.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":105105987,"end":105106094,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000265499.1","gene_symbol":"MIR3156-2","gene_name":"microRNA 3156-2 [Source:HGNC Symbol;Acc:HGNC:38213]","synonyms":"hsa-mir-3156-2","biotype":"miRNA","ncbi_id":"100422907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14830166,"end":14830242,"strand":1,"description":"microRNA 3156-2 [Source:HGNC Symbol;Acc:HGNC:38213]"}, {"versioned_ensembl_gene_id":"ENSG00000207649.3","gene_symbol":"MIR138-2","gene_name":"microRNA 138-2 [Source:HGNC Symbol;Acc:HGNC:31525]","synonyms":"MIRN138-2,hsa-mir-138-2","biotype":"miRNA","ncbi_id":"406930","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56858518,"end":56858601,"strand":1,"description":"microRNA 138-2 [Source:HGNC Symbol;Acc:HGNC:31525]"}, {"versioned_ensembl_gene_id":"ENSG00000284186.1","gene_symbol":"MIR3615","gene_name":"microRNA 3615 [Source:HGNC Symbol;Acc:HGNC:38905]","synonyms":"hsa-mir-3615","biotype":"miRNA","ncbi_id":"100500847","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74748613,"end":74748699,"strand":1,"description":"microRNA 3615 [Source:HGNC Symbol;Acc:HGNC:38905]"}, {"versioned_ensembl_gene_id":"ENSG00000207606.1","gene_symbol":"MIR554","gene_name":"microRNA 554 [Source:HGNC Symbol;Acc:HGNC:32810]","synonyms":"MIRN554,hsa-mir-554","biotype":"miRNA","ncbi_id":"693139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151545796,"end":151545891,"strand":1,"description":"microRNA 554 [Source:HGNC Symbol;Acc:HGNC:32810]"}, {"versioned_ensembl_gene_id":"ENSG00000198974.3","gene_symbol":"MIR30E","gene_name":"microRNA 30e [Source:HGNC Symbol;Acc:HGNC:31629]","synonyms":"MIRN30E,hsa-mir-30e","biotype":"miRNA","ncbi_id":"407034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40754355,"end":40754446,"strand":1,"description":"microRNA 30e [Source:HGNC Symbol;Acc:HGNC:31629]"}, {"versioned_ensembl_gene_id":"ENSG00000200413.1","gene_symbol":"SNORD114-26","gene_name":"small nucleolar RNA, C/D box 114-26 [Source:HGNC Symbol;Acc:HGNC:33014]","synonyms":"14q(II-26)","biotype":"snoRNA","ncbi_id":"767606","summary":null,"start":100987046,"end":100987117,"strand":1,"description":"small nucleolar RNA, C/D box 114-26 [Source:HGNC Symbol;Acc:HGNC:33014]"}, {"versioned_ensembl_gene_id":"ENSG00000252357.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":173808489,"end":173808622,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280280.1","gene_symbol":"AC006435.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2460183,"end":2460294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263652.1","gene_symbol":"MIR548AX","gene_name":"microRNA 548ax [Source:HGNC Symbol;Acc:HGNC:43528]","synonyms":"hsa-mir-548ax","biotype":"miRNA","ncbi_id":"100847063","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11318614,"end":11318686,"strand":-1,"description":"microRNA 548ax [Source:HGNC Symbol;Acc:HGNC:43528]"}, {"versioned_ensembl_gene_id":"ENSG00000277264.1","gene_symbol":"MIR6833","gene_name":"microRNA 6833 [Source:HGNC Symbol;Acc:HGNC:50245]","synonyms":"hsa-mir-6833","biotype":"miRNA","ncbi_id":"102465500","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32179816,"end":32179876,"strand":1,"description":"microRNA 6833 [Source:HGNC Symbol;Acc:HGNC:50245]"}, {"versioned_ensembl_gene_id":"ENSG00000277179.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54929128,"end":54953124,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000264661.3","gene_symbol":"MIR3200","gene_name":"microRNA 3200 [Source:HGNC Symbol;Acc:HGNC:38227]","synonyms":"hsa-mir-3200","biotype":"miRNA","ncbi_id":"100422912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30731557,"end":30731641,"strand":1,"description":"microRNA 3200 [Source:HGNC Symbol;Acc:HGNC:38227]"}, {"versioned_ensembl_gene_id":"ENSG00000283894.1","gene_symbol":"MIR1324","gene_name":"microRNA 1324 [Source:HGNC Symbol;Acc:HGNC:35377]","synonyms":"MIRN1324,hsa-mir-1324","biotype":"miRNA","ncbi_id":"100302212","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75630763,"end":75630858,"strand":1,"description":"microRNA 1324 [Source:HGNC Symbol;Acc:HGNC:35377]"}, {"versioned_ensembl_gene_id":"ENSG00000265301.1","gene_symbol":"MIR548AD","gene_name":"microRNA 548ad [Source:HGNC Symbol;Acc:HGNC:41683]","synonyms":"hsa-mir-548ad","biotype":"miRNA","ncbi_id":"100616475","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35471405,"end":35471486,"strand":1,"description":"microRNA 548ad [Source:HGNC Symbol;Acc:HGNC:41683]"}, {"versioned_ensembl_gene_id":"ENSG00000275950.1","gene_symbol":"MIR6724-1","gene_name":"microRNA 6724-1 [Source:HGNC Symbol;Acc:HGNC:50837]","synonyms":null,"biotype":"miRNA","ncbi_id":"102465433","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8205315,"end":8205406,"strand":1,"description":"microRNA 6724-1 [Source:HGNC Symbol;Acc:HGNC:50837]"}, {"versioned_ensembl_gene_id":"ENSG00000264405.1","gene_symbol":"MIR3913-1","gene_name":"microRNA 3913-1 [Source:HGNC Symbol;Acc:HGNC:38884]","synonyms":"hsa-mir-3913-1","biotype":"miRNA","ncbi_id":"100500903","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69584722,"end":69584823,"strand":-1,"description":"microRNA 3913-1 [Source:HGNC Symbol;Acc:HGNC:38884]"}, {"versioned_ensembl_gene_id":"ENSG00000265526.1","gene_symbol":"MIR4304","gene_name":"microRNA 4304 [Source:HGNC Symbol;Acc:HGNC:38276]","synonyms":"hsa-mir-4304","biotype":"miRNA","ncbi_id":"100422931","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123010667,"end":123010728,"strand":-1,"description":"microRNA 4304 [Source:HGNC Symbol;Acc:HGNC:38276]"}, {"versioned_ensembl_gene_id":"ENSG00000185222.8","gene_symbol":"TCEAL9","gene_name":"transcription elongation factor A like 9 [Source:HGNC Symbol;Acc:HGNC:30084]","synonyms":"WEX6,WBP5,DKFZp313K1940","biotype":"protein_coding","ncbi_id":"51186","summary":"The globular WW domain is composed of 38 to 40 semiconserved amino acids shared by proteins of diverse functions including structural, regulatory, and signaling proteins. The domain is involved in mediating protein-protein interactions through the binding of polyproline ligands. This gene encodes a WW domain binding protein. This gene also encodes a domain with similarity to the transcription elongation factor A, SII-related family. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]","start":103356452,"end":103358451,"strand":1,"description":"transcription elongation factor A like 9 [Source:HGNC Symbol;Acc:HGNC:30084]"}, {"versioned_ensembl_gene_id":"ENSG00000199584.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127619336,"end":127619447,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252470.1","gene_symbol":"RNU6-551P","gene_name":"RNA, U6 small nuclear 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:47514]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479811","summary":null,"start":107435118,"end":107435220,"strand":1,"description":"RNA, U6 small nuclear 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:47514]"}, {"versioned_ensembl_gene_id":"ENSG00000277599.1","gene_symbol":"NEAT1_3","gene_name":"Nuclear enriched abundant transcript 1 conserved region 3 [Source:RFAM;Acc:RF01957]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423960,"end":65424118,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 3 [Source:RFAM;Acc:RF01957]"}, {"versioned_ensembl_gene_id":"ENSG00000283489.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":132525809,"end":132525887,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000240299.3","gene_symbol":"RN7SL187P","gene_name":"RNA, 7SL, cytoplasmic 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:46203]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481829","summary":null,"start":121494519,"end":121494821,"strand":1,"description":"RNA, 7SL, cytoplasmic 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:46203]"}, {"versioned_ensembl_gene_id":"ENSG00000252173.1","gene_symbol":"RNU6-109P","gene_name":"RNA, U6 small nuclear 109, pseudogene [Source:HGNC Symbol;Acc:HGNC:47072]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481211","summary":null,"start":16248935,"end":16249041,"strand":1,"description":"RNA, U6 small nuclear 109, pseudogene [Source:HGNC Symbol;Acc:HGNC:47072]"}, {"versioned_ensembl_gene_id":"ENSG00000199687.1","gene_symbol":"RNU1-38P","gene_name":"RNA, U1 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48380]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481608","summary":null,"start":85728194,"end":85728337,"strand":-1,"description":"RNA, U1 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48380]"}, {"versioned_ensembl_gene_id":"ENSG00000201245.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"ACA25,SNORA25A","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":99783857,"end":99783983,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000207005.1","gene_symbol":"RNU1-2","gene_name":"RNA, U1 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10123]","synonyms":"RNU1C2,RNU1C1,U1C21,U1C1","biotype":"snRNA","ncbi_id":"26870","summary":null,"start":16895980,"end":16896143,"strand":1,"description":"RNA, U1 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10123]"}, {"versioned_ensembl_gene_id":"ENSG00000212338.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"U67,RNU67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":179196473,"end":179196579,"strand":1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000200350.1","gene_symbol":"RNU6-1285P","gene_name":"RNA, U6 small nuclear 1285, pseudogene [Source:HGNC Symbol;Acc:HGNC:48248]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481948","summary":null,"start":154543933,"end":154544037,"strand":-1,"description":"RNA, U6 small nuclear 1285, pseudogene [Source:HGNC Symbol;Acc:HGNC:48248]"}, {"versioned_ensembl_gene_id":"ENSG00000201207.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31663288,"end":31663401,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243365.3","gene_symbol":"RN7SL278P","gene_name":"RNA, 7SL, cytoplasmic 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:46294]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479324","summary":null,"start":76976915,"end":76977210,"strand":-1,"description":"RNA, 7SL, cytoplasmic 278, pseudogene [Source:HGNC Symbol;Acc:HGNC:46294]"}, {"versioned_ensembl_gene_id":"ENSG00000212479.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29180425,"end":29180639,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252837.1","gene_symbol":"RN7SKP99","gene_name":"RNA, 7SK small nuclear pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:45823]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479138","summary":null,"start":57837354,"end":57837660,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:45823]"}, {"versioned_ensembl_gene_id":"ENSG00000275420.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69478716,"end":69478984,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000223086.1","gene_symbol":"RNA5SP155","gene_name":"RNA, 5S ribosomal pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:43055]","synonyms":"RN5S155","biotype":"rRNA","ncbi_id":"100873421","summary":null,"start":10115756,"end":10115884,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:43055]"}, {"versioned_ensembl_gene_id":"ENSG00000274873.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000273770.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78544095,"end":78544188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201370.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":16623004,"end":16623095,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200057.1","gene_symbol":"RN7SKP63","gene_name":"RNA, 7SK small nuclear pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:45787]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479123","summary":null,"start":21389191,"end":21389491,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:45787]"}, {"versioned_ensembl_gene_id":"ENSG00000276902.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6365955,"end":6366055,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275319.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18524620,"end":18524935,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252191.1","gene_symbol":"RNU6-751P","gene_name":"RNA, U6 small nuclear 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:47714]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479898","summary":null,"start":53749851,"end":53749951,"strand":-1,"description":"RNA, U6 small nuclear 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:47714]"}, {"versioned_ensembl_gene_id":"ENSG00000277400.1","gene_symbol":"AC145212.2","gene_name":"MaFF-interacting protein [Source:UniProtKB/Swiss-Prot;Acc:Q8WZ33]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53590,"end":115018,"strand":-1,"description":"MaFF-interacting protein [Source:UniProtKB/Swiss-Prot;Acc:Q8WZ33]"}, {"versioned_ensembl_gene_id":"ENSG00000251764.1","gene_symbol":"RNA5SP446","gene_name":"RNA, 5S ribosomal pseudogene 446 [Source:HGNC Symbol;Acc:HGNC:43346]","synonyms":"RN5S446","biotype":"rRNA","ncbi_id":"100873692","summary":null,"start":66895491,"end":66895572,"strand":1,"description":"RNA, 5S ribosomal pseudogene 446 [Source:HGNC Symbol;Acc:HGNC:43346]"}, {"versioned_ensembl_gene_id":"ENSG00000264322.2","gene_symbol":"RN7SL448P","gene_name":"RNA, 7SL, cytoplasmic 448, pseudogene [Source:HGNC 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are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010]","start":6967337,"end":6967606,"strand":-1,"description":"small Cajal body-specific RNA 12 [Source:HGNC Symbol;Acc:HGNC:32569]"}, {"versioned_ensembl_gene_id":"ENSG00000264275.1","gene_symbol":"RN7SL753P","gene_name":"RNA, 7SL, cytoplasmic 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:46769]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479496","summary":null,"start":202333439,"end":202333728,"strand":1,"description":"RNA, 7SL, cytoplasmic 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:46769]"}, {"versioned_ensembl_gene_id":"ENSG00000252464.1","gene_symbol":"RN7SKP70","gene_name":"RNA, 7SK small nuclear pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:45794]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107057644","summary":null,"start":178619728,"end":178619998,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:45794]"}, {"versioned_ensembl_gene_id":"ENSG00000251830.1","gene_symbol":"SNORD46","gene_name":"Small 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{"versioned_ensembl_gene_id":"ENSG00000200708.1","gene_symbol":"RN7SKP93","gene_name":"RNA, 7SK small nuclear pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:45817]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479136","summary":null,"start":133596091,"end":133596399,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:45817]"}, {"versioned_ensembl_gene_id":"ENSG00000239545.3","gene_symbol":"RN7SL822P","gene_name":"RNA, 7SL, cytoplasmic 822, pseudogene [Source:HGNC Symbol;Acc:HGNC:46838]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479521","summary":null,"start":55215624,"end":55215919,"strand":-1,"description":"RNA, 7SL, cytoplasmic 822, pseudogene [Source:HGNC Symbol;Acc:HGNC:46838]"}, {"versioned_ensembl_gene_id":"ENSG00000244091.1","gene_symbol":"RN7SL483P","gene_name":"RNA, 7SL, cytoplasmic 483, pseudogene [Source:HGNC 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[provided by RefSeq, Sep 2009]","start":140732564,"end":140732653,"strand":-1,"description":"microRNA 151a [Source:HGNC Symbol;Acc:HGNC:31762]"}, {"versioned_ensembl_gene_id":"ENSG00000283522.1","gene_symbol":"MIR3150A","gene_name":"microRNA 3150a [Source:HGNC Symbol;Acc:HGNC:38362]","synonyms":"MIR3150,hsa-mir-3150a,hsa-mir-3150","biotype":"miRNA","ncbi_id":"100422964","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95072914,"end":95072993,"strand":1,"description":"microRNA 3150a [Source:HGNC Symbol;Acc:HGNC:38362]"}, {"versioned_ensembl_gene_id":"ENSG00000222881.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40391232,"end":40391338,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265520.1","gene_symbol":"MIR548V","gene_name":"microRNA 548v [Source:HGNC Symbol;Acc:HGNC:38302]","synonyms":"hsa-mir-548v","biotype":"miRNA","ncbi_id":"100422850","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17681578,"end":17681657,"strand":-1,"description":"microRNA 548v [Source:HGNC Symbol;Acc:HGNC:38302]"}, {"versioned_ensembl_gene_id":"ENSG00000222764.1","gene_symbol":"RN7SKP106","gene_name":"RNA, 7SK small nuclear pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:45830]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479142","summary":null,"start":141486141,"end":141486412,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:45830]"}, {"versioned_ensembl_gene_id":"ENSG00000264732.1","gene_symbol":"MIR4638","gene_name":"microRNA 4638 [Source:HGNC Symbol;Acc:HGNC:41841]","synonyms":"hsa-mir-4638","biotype":"miRNA","ncbi_id":"100616342","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":181222566,"end":181222633,"strand":-1,"description":"microRNA 4638 [Source:HGNC Symbol;Acc:HGNC:41841]"}, {"versioned_ensembl_gene_id":"ENSG00000201240.1","gene_symbol":"SNORD114-9","gene_name":"small nucleolar RNA, C/D box 114-9 [Source:HGNC Symbol;Acc:HGNC:32997]","synonyms":"14q(II-9)","biotype":"snoRNA","ncbi_id":"767585","summary":null,"start":100966029,"end":100966100,"strand":1,"description":"small nucleolar RNA, C/D box 114-9 [Source:HGNC Symbol;Acc:HGNC:32997]"}, {"versioned_ensembl_gene_id":"ENSG00000266698.1","gene_symbol":"MIR3945","gene_name":"microRNA 3945 [Source:HGNC Symbol;Acc:HGNC:38954]","synonyms":"hsa-mir-3945","biotype":"miRNA","ncbi_id":"100500818","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":184851013,"end":184851110,"strand":-1,"description":"microRNA 3945 [Source:HGNC Symbol;Acc:HGNC:38954]"}, {"versioned_ensembl_gene_id":"ENSG00000264494.1","gene_symbol":"MIR4650-2","gene_name":"microRNA 4650-2 [Source:HGNC Symbol;Acc:HGNC:41810]","synonyms":"hsa-mir-4650-2","biotype":"miRNA","ncbi_id":"100616331","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72697903,"end":72697978,"strand":1,"description":"microRNA 4650-2 [Source:HGNC Symbol;Acc:HGNC:41810]"}, {"versioned_ensembl_gene_id":"ENSG00000283275.1","gene_symbol":"MIR4275","gene_name":"microRNA 4275 [Source:HGNC Symbol;Acc:HGNC:38293]","synonyms":"hsa-mir-4275","biotype":"miRNA","ncbi_id":"100422937","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28819582,"end":28819668,"strand":1,"description":"microRNA 4275 [Source:HGNC Symbol;Acc:HGNC:38293]"}, {"versioned_ensembl_gene_id":"ENSG00000201314.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":145958128,"end":145958240,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201649.1","gene_symbol":"RNY4P34","gene_name":"RNA, Ro-associated Y4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:50882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481712","summary":null,"start":200373175,"end":200373269,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:50882]"}, {"versioned_ensembl_gene_id":"ENSG00000200288.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":177624282,"end":177624409,"strand":-1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000283733.1","gene_symbol":"MIR146A","gene_name":"microRNA 146a [Source:HGNC Symbol;Acc:HGNC:31533]","synonyms":"MIRN146A,MIRN146,hsa-mir-146a,hsa-mir-146","biotype":"miRNA","ncbi_id":"406938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. Some of the targets of the encoded miRNA are the transcripts for tumor necrosis factor, interleukin 1 receptor-associated kinase 1, interleukin 1-beta, TNF receptor-associated factor 6, and complement factor H. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2015]","start":160485352,"end":160485450,"strand":1,"description":"microRNA 146a [Source:HGNC Symbol;Acc:HGNC:31533]"}, {"versioned_ensembl_gene_id":"ENSG00000273709.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43241180,"end":43241370,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000275523.1","gene_symbol":"MIR6508","gene_name":"microRNA 6508 [Source:HGNC Symbol;Acc:HGNC:50217]","synonyms":"hsa-mir-6508","biotype":"miRNA","ncbi_id":"102466972","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39447010,"end":39447069,"strand":1,"description":"microRNA 6508 [Source:HGNC Symbol;Acc:HGNC:50217]"}, {"versioned_ensembl_gene_id":"ENSG00000277671.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8250060,"end":8250149,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000252139.1","gene_symbol":"SCARNA18","gene_name":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]","synonyms":"U109,SCARNA18A","biotype":"scaRNA","ncbi_id":"677765","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":49814361,"end":49814443,"strand":1,"description":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]"}, {"versioned_ensembl_gene_id":"ENSG00000222378.1","gene_symbol":"RNA5SP44","gene_name":"RNA, 5S ribosomal pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:42820]","synonyms":"RN5S44","biotype":"rRNA","ncbi_id":"100873283","summary":null,"start":39154164,"end":39154296,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:42820]"}, {"versioned_ensembl_gene_id":"ENSG00000212205.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":211803017,"end":211803104,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265321.1","gene_symbol":"MIR4263","gene_name":"microRNA 4263 [Source:HGNC Symbol;Acc:HGNC:38365]","synonyms":"hsa-mir-4263","biotype":"miRNA","ncbi_id":"100422965","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27996367,"end":27996449,"strand":1,"description":"microRNA 4263 [Source:HGNC Symbol;Acc:HGNC:38365]"}, {"versioned_ensembl_gene_id":"ENSG00000199788.1","gene_symbol":"RNY3P2","gene_name":"RNA, Ro-associated Y3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42486]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862668","summary":null,"start":49095391,"end":49095492,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42486]"}, {"versioned_ensembl_gene_id":"ENSG00000199143.1","gene_symbol":"MIR373","gene_name":"microRNA 373 [Source:HGNC Symbol;Acc:HGNC:31787]","synonyms":"MIRN373,hsa-mir-373","biotype":"miRNA","ncbi_id":"442918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53788705,"end":53788773,"strand":1,"description":"microRNA 373 [Source:HGNC Symbol;Acc:HGNC:31787]"}, {"versioned_ensembl_gene_id":"ENSG00000284031.1","gene_symbol":"MIR4761","gene_name":"microRNA 4761 [Source:HGNC Symbol;Acc:HGNC:41591]","synonyms":"hsa-mir-4761","biotype":"miRNA","ncbi_id":"100616414","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19963753,"end":19963834,"strand":1,"description":"microRNA 4761 [Source:HGNC Symbol;Acc:HGNC:41591]"}, {"versioned_ensembl_gene_id":"ENSG00000266649.1","gene_symbol":"MIR3126","gene_name":"microRNA 3126 [Source:HGNC Symbol;Acc:HGNC:38225]","synonyms":"hsa-mir-3126","biotype":"miRNA","ncbi_id":"100423030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69103682,"end":69103755,"strand":1,"description":"microRNA 3126 [Source:HGNC Symbol;Acc:HGNC:38225]"}, {"versioned_ensembl_gene_id":"ENSG00000222293.1","gene_symbol":"RNU2-36P","gene_name":"RNA, U2 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48529]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481645","summary":null,"start":86422938,"end":86423128,"strand":-1,"description":"RNA, U2 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:48529]"}, {"versioned_ensembl_gene_id":"ENSG00000207511.1","gene_symbol":"RNU6-443P","gene_name":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481318","summary":null,"start":13279125,"end":13279231,"strand":-1,"description":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]"}, {"versioned_ensembl_gene_id":"ENSG00000264113.2","gene_symbol":"RN7SL784P","gene_name":"RNA, 7SL, cytoplasmic 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:46800]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481134","summary":null,"start":4882975,"end":4883316,"strand":1,"description":"RNA, 7SL, cytoplasmic 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:46800]"}, {"versioned_ensembl_gene_id":"ENSG00000207761.3","gene_symbol":"MIR329-1","gene_name":"microRNA 329-1 [Source:HGNC Symbol;Acc:HGNC:32050]","synonyms":"MIRN329-1,hsa-mir-329-1","biotype":"miRNA","ncbi_id":"574408","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101026785,"end":101026864,"strand":1,"description":"microRNA 329-1 [Source:HGNC Symbol;Acc:HGNC:32050]"}, {"versioned_ensembl_gene_id":"ENSG00000284269.1","gene_symbol":"MIR7855","gene_name":"microRNA 7855 [Source:HGNC Symbol;Acc:HGNC:50244]","synonyms":"hsa-mir-7855","biotype":"miRNA","ncbi_id":"102465841","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64785626,"end":64785686,"strand":-1,"description":"microRNA 7855 [Source:HGNC Symbol;Acc:HGNC:50244]"}, {"versioned_ensembl_gene_id":"ENSG00000283785.1","gene_symbol":"MIR15A","gene_name":"microRNA 15a [Source:HGNC Symbol;Acc:HGNC:31543]","synonyms":"MIRN15A,hsa-mir-15a","biotype":"miRNA","ncbi_id":"406948","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50049119,"end":50049201,"strand":-1,"description":"microRNA 15a [Source:HGNC Symbol;Acc:HGNC:31543]"}, {"versioned_ensembl_gene_id":"ENSG00000201523.1","gene_symbol":"RNA5SP205","gene_name":"RNA, 5S ribosomal pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:43105]","synonyms":"RN5S205","biotype":"rRNA","ncbi_id":"100873466","summary":null,"start":19438283,"end":19438418,"strand":1,"description":"RNA, 5S ribosomal pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:43105]"}, {"versioned_ensembl_gene_id":"ENSG00000238964.1","gene_symbol":"RNU7-125P","gene_name":"RNA, U7 small nuclear 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:45659]","synonyms":"RNU7-135P","biotype":"snRNA","ncbi_id":"106480818","summary":null,"start":14643788,"end":14643849,"strand":1,"description":"RNA, U7 small nuclear 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:45659]"}, {"versioned_ensembl_gene_id":"ENSG00000221540.1","gene_symbol":"MIR1180","gene_name":"microRNA 1180 [Source:HGNC Symbol;Acc:HGNC:35261]","synonyms":"hsa-mir-1180,MIRN1180","biotype":"miRNA","ncbi_id":"100302256","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19344506,"end":19344574,"strand":-1,"description":"microRNA 1180 [Source:HGNC Symbol;Acc:HGNC:35261]"}, {"versioned_ensembl_gene_id":"ENSG00000199409.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":150098406,"end":150098506,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264906.1","gene_symbol":"MIR4494","gene_name":"microRNA 4494 [Source:HGNC Symbol;Acc:HGNC:41731]","synonyms":"hsa-mir-4494","biotype":"miRNA","ncbi_id":"100616478","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47364186,"end":47364269,"strand":-1,"description":"microRNA 4494 [Source:HGNC Symbol;Acc:HGNC:41731]"}, {"versioned_ensembl_gene_id":"ENSG00000207375.1","gene_symbol":"SNORD116-23","gene_name":"small nucleolar RNA, C/D box 116-23 [Source:HGNC Symbol;Acc:HGNC:33089]","synonyms":"HBII-85-23","biotype":"snoRNA","ncbi_id":"100033434","summary":null,"start":25091786,"end":25091877,"strand":1,"description":"small nucleolar RNA, C/D box 116-23 [Source:HGNC Symbol;Acc:HGNC:33089]"}, {"versioned_ensembl_gene_id":"ENSG00000200361.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":106688678,"end":106688779,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277243.1","gene_symbol":"MIR3118-3","gene_name":"microRNA 3118-3 [Source:HGNC Symbol;Acc:HGNC:38274]","synonyms":"hsa-mir-3118-3","biotype":"miRNA","ncbi_id":"100422844","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21406385,"end":21406459,"strand":1,"description":"microRNA 3118-3 [Source:HGNC Symbol;Acc:HGNC:38274]"}, {"versioned_ensembl_gene_id":"ENSG00000202257.1","gene_symbol":"RNA5S16","gene_name":"RNA, 5S ribosomal 16 [Source:HGNC Symbol;Acc:HGNC:34377]","synonyms":"RN5S16","biotype":"rRNA","ncbi_id":"100169767","summary":null,"start":228643809,"end":228643927,"strand":-1,"description":"RNA, 5S ribosomal 16 [Source:HGNC Symbol;Acc:HGNC:34377]"}, {"versioned_ensembl_gene_id":"ENSG00000265719.1","gene_symbol":"MIR4681","gene_name":"microRNA 4681 [Source:HGNC Symbol;Acc:HGNC:41753]","synonyms":"hsa-mir-4681","biotype":"miRNA","ncbi_id":"100616398","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119377972,"end":119378043,"strand":1,"description":"microRNA 4681 [Source:HGNC Symbol;Acc:HGNC:41753]"}, {"versioned_ensembl_gene_id":"ENSG00000277634.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49839401,"end":49839493,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207242.1","gene_symbol":"RNU6-1065P","gene_name":"RNA, U6 small nuclear 1065, pseudogene [Source:HGNC Symbol;Acc:HGNC:48028]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480034","summary":null,"start":10857899,"end":10858004,"strand":-1,"description":"RNA, U6 small nuclear 1065, pseudogene [Source:HGNC Symbol;Acc:HGNC:48028]"}, {"versioned_ensembl_gene_id":"ENSG00000274196.4","gene_symbol":"FAM197Y4","gene_name":"family with sequence similarity 197 Y-linked member 4 [Source:HGNC Symbol;Acc:HGNC:37466]","synonyms":"FAM197Y4P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100289188","summary":null,"start":9479053,"end":9486239,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 4 [Source:HGNC Symbol;Acc:HGNC:37466]"}, {"versioned_ensembl_gene_id":"ENSG00000242206.2","gene_symbol":"AP004217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118761856,"end":118762201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273997.1","gene_symbol":"AL355365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147406531,"end":147406824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274056.1","gene_symbol":"MIR6507","gene_name":"microRNA 6507 [Source:HGNC Symbol;Acc:HGNC:50199]","synonyms":"hsa-mir-6507","biotype":"miRNA","ncbi_id":"102465253","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98924499,"end":98924568,"strand":-1,"description":"microRNA 6507 [Source:HGNC Symbol;Acc:HGNC:50199]"}, {"versioned_ensembl_gene_id":"ENSG00000284122.1","gene_symbol":"MIR6717","gene_name":"microRNA 6717 [Source:HGNC Symbol;Acc:HGNC:50000]","synonyms":"hsa-mir-6717","biotype":"miRNA","ncbi_id":"102465428","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21023314,"end":21023386,"strand":-1,"description":"microRNA 6717 [Source:HGNC Symbol;Acc:HGNC:50000]"}, {"versioned_ensembl_gene_id":"ENSG00000274202.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":93197,"end":93309,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000278281.1","gene_symbol":"MIR7856","gene_name":"microRNA 7856 [Source:HGNC Symbol;Acc:HGNC:50268]","synonyms":"hsa-mir-7856","biotype":"miRNA","ncbi_id":"102465842","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86357632,"end":86357687,"strand":-1,"description":"microRNA 7856 [Source:HGNC Symbol;Acc:HGNC:50268]"}, {"versioned_ensembl_gene_id":"ENSG00000284425.1","gene_symbol":"MIR8072","gene_name":"microRNA 8072 [Source:HGNC Symbol;Acc:HGNC:50174]","synonyms":"hsa-mir-8072","biotype":"miRNA","ncbi_id":"102466877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123364764,"end":123364843,"strand":-1,"description":"microRNA 8072 [Source:HGNC Symbol;Acc:HGNC:50174]"}, {"versioned_ensembl_gene_id":"ENSG00000207402.1","gene_symbol":"RNU6-959P","gene_name":"RNA, U6 small nuclear 959, pseudogene [Source:HGNC Symbol;Acc:HGNC:47922]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479990","summary":null,"start":191121950,"end":191122056,"strand":1,"description":"RNA, U6 small nuclear 959, pseudogene [Source:HGNC Symbol;Acc:HGNC:47922]"}, {"versioned_ensembl_gene_id":"ENSG00000278715.1","gene_symbol":"SNORD116-20","gene_name":"small nucleolar RNA, C/D box 116-20 [Source:HGNC Symbol;Acc:HGNC:33086]","synonyms":"HBII-85-20","biotype":"snoRNA","ncbi_id":"100033431","summary":null,"start":25087662,"end":25087753,"strand":1,"description":"small nucleolar RNA, C/D box 116-20 [Source:HGNC Symbol;Acc:HGNC:33086]"}, {"versioned_ensembl_gene_id":"ENSG00000263426.2","gene_symbol":"RN7SL471P","gene_name":"RNA, 7SL, cytoplasmic 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:46487]","synonyms":"RN7SL257P","biotype":"misc_RNA","ncbi_id":"106481051","summary":null,"start":28977475,"end":28977773,"strand":1,"description":"RNA, 7SL, cytoplasmic 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:46487]"}, {"versioned_ensembl_gene_id":"ENSG00000207108.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185630428,"end":185630528,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252863.1","gene_symbol":"RNU6-1183P","gene_name":"RNA, U6 small nuclear 1183, pseudogene [Source:HGNC Symbol;Acc:HGNC:48146]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481941","summary":null,"start":101871742,"end":101871801,"strand":-1,"description":"RNA, U6 small nuclear 1183, pseudogene [Source:HGNC Symbol;Acc:HGNC:48146]"}, {"versioned_ensembl_gene_id":"ENSG00000222741.1","gene_symbol":"RNA5SP229","gene_name":"RNA, 5S ribosomal pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:43129]","synonyms":"RN5S229","biotype":"rRNA","ncbi_id":"100873487","summary":null,"start":33177740,"end":33177838,"strand":1,"description":"RNA, 5S ribosomal pseudogene 229 [Source:HGNC Symbol;Acc:HGNC:43129]"}, {"versioned_ensembl_gene_id":"ENSG00000278115.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32682415,"end":32682705,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200422.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":87146733,"end":87146804,"strand":1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000264218.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747847,"end":29747948,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202093.1","gene_symbol":"SNORD58C","gene_name":"small nucleolar RNA, C/D box 58C [Source:HGNC Symbol;Acc:HGNC:33613]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124516","summary":null,"start":49489245,"end":49489308,"strand":-1,"description":"small nucleolar RNA, C/D box 58C [Source:HGNC Symbol;Acc:HGNC:33613]"}, {"versioned_ensembl_gene_id":"ENSG00000277233.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48429269,"end":48429554,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222515.1","gene_symbol":"RN7SKP240","gene_name":"RNA, 7SK small nuclear pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:45964]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479202","summary":null,"start":22085544,"end":22085918,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:45964]"}, {"versioned_ensembl_gene_id":"ENSG00000223274.6","gene_symbol":"RNA5SP498","gene_name":"RNA, 5S ribosomal pseudogene 498 [Source:HGNC Symbol;Acc:HGNC:43398]","synonyms":"RN5S498","biotype":"rRNA","ncbi_id":"106480770","summary":null,"start":1300256,"end":1300375,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 498 [Source:HGNC Symbol;Acc:HGNC:43398]"}, {"versioned_ensembl_gene_id":"ENSG00000159712.10","gene_symbol":"ANKRD18CP","gene_name":"ankyrin repeat domain 18C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43601]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101926917","summary":null,"start":97156570,"end":97221235,"strand":-1,"description":"ankyrin repeat domain 18C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43601]"}, {"versioned_ensembl_gene_id":"ENSG00000263972.1","gene_symbol":"MIR1587","gene_name":"microRNA 1587 [Source:HGNC Symbol;Acc:HGNC:41596]","synonyms":"hsa-mir-1587","biotype":"miRNA","ncbi_id":"100616251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39837561,"end":39837613,"strand":1,"description":"microRNA 1587 [Source:HGNC Symbol;Acc:HGNC:41596]"}, {"versioned_ensembl_gene_id":"ENSG00000278704.1","gene_symbol":"BX004987.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56140,"end":58376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284176.1","gene_symbol":"MIR5090","gene_name":"microRNA 5090 [Source:HGNC Symbol;Acc:HGNC:43547]","synonyms":"hsa-mir-5090","biotype":"miRNA","ncbi_id":"100847073","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102465742,"end":102465826,"strand":1,"description":"microRNA 5090 [Source:HGNC Symbol;Acc:HGNC:43547]"}, {"versioned_ensembl_gene_id":"ENSG00000200620.1","gene_symbol":"SNORA7","gene_name":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15716208,"end":15716346,"strand":1,"description":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]"}, {"versioned_ensembl_gene_id":"ENSG00000201596.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185634073,"end":185634182,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221039.3","gene_symbol":"MIR1286","gene_name":"microRNA 1286 [Source:HGNC Symbol;Acc:HGNC:35279]","synonyms":"MIRN1286,hsa-mir-1286","biotype":"miRNA","ncbi_id":"100302118","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20249134,"end":20249211,"strand":-1,"description":"microRNA 1286 [Source:HGNC Symbol;Acc:HGNC:35279]"}, {"versioned_ensembl_gene_id":"ENSG00000222852.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":180909838,"end":180909927,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207150.1","gene_symbol":"RNU6-185P","gene_name":"RNA, U6 small nuclear 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:47148]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481235","summary":null,"start":87474183,"end":87474289,"strand":-1,"description":"RNA, U6 small nuclear 185, pseudogene [Source:HGNC Symbol;Acc:HGNC:47148]"}, {"versioned_ensembl_gene_id":"ENSG00000275745.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66550457,"end":66550567,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284453.1","gene_symbol":"MIR1-2","gene_name":"microRNA 1-2 [Source:HGNC Symbol;Acc:HGNC:31500]","synonyms":"MIRN1-2,hsa-mir-1-2","biotype":"miRNA","ncbi_id":"406905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21829004,"end":21829088,"strand":-1,"description":"microRNA 1-2 [Source:HGNC Symbol;Acc:HGNC:31500]"}, {"versioned_ensembl_gene_id":"ENSG00000283774.1","gene_symbol":"MIR632","gene_name":"microRNA 632 [Source:HGNC Symbol;Acc:HGNC:32888]","synonyms":"MIRN632,hsa-mir-632","biotype":"miRNA","ncbi_id":"693217","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32350109,"end":32350202,"strand":1,"description":"microRNA 632 [Source:HGNC Symbol;Acc:HGNC:32888]"}, {"versioned_ensembl_gene_id":"ENSG00000264092.2","gene_symbol":"RN7SL474P","gene_name":"RNA, 7SL, cytoplasmic 474, pseudogene [Source:HGNC Symbol;Acc:HGNC:46490]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481052","summary":null,"start":16863196,"end":16863496,"strand":-1,"description":"RNA, 7SL, cytoplasmic 474, pseudogene [Source:HGNC Symbol;Acc:HGNC:46490]"}, {"versioned_ensembl_gene_id":"ENSG00000242707.3","gene_symbol":"RN7SL362P","gene_name":"RNA, 7SL, cytoplasmic 362, pseudogene [Source:HGNC Symbol;Acc:HGNC:46378]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481022","summary":null,"start":13715102,"end":13715368,"strand":-1,"description":"RNA, 7SL, cytoplasmic 362, pseudogene [Source:HGNC Symbol;Acc:HGNC:46378]"}, {"versioned_ensembl_gene_id":"ENSG00000221245.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"SNORA11A,U107","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":119569699,"end":119569825,"strand":1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000280049.1","gene_symbol":"AC079597.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87041916,"end":87042423,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280009.1","gene_symbol":"AC020923.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86305233,"end":86306149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266426.1","gene_symbol":"MIR4719","gene_name":"microRNA 4719 [Source:HGNC Symbol;Acc:HGNC:41807]","synonyms":"hsa-mir-4719","biotype":"miRNA","ncbi_id":"100616172","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76868936,"end":76869019,"strand":1,"description":"microRNA 4719 [Source:HGNC Symbol;Acc:HGNC:41807]"}, {"versioned_ensembl_gene_id":"ENSG00000238500.1","gene_symbol":"RNU7-87P","gene_name":"RNA, U7 small nuclear 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:42616]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873842","summary":null,"start":66630715,"end":66630776,"strand":-1,"description":"RNA, U7 small nuclear 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:42616]"}, {"versioned_ensembl_gene_id":"ENSG00000201622.1","gene_symbol":"RNU6-621P","gene_name":"RNA, U6 small nuclear 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:47584]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481907","summary":null,"start":197994601,"end":197994709,"strand":1,"description":"RNA, U6 small nuclear 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:47584]"}, {"versioned_ensembl_gene_id":"ENSG00000201826.1","gene_symbol":"RNU6-867P","gene_name":"RNA, U6 small nuclear 867, pseudogene [Source:HGNC Symbol;Acc:HGNC:47830]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479949","summary":null,"start":76244968,"end":76245074,"strand":1,"description":"RNA, U6 small nuclear 867, pseudogene [Source:HGNC Symbol;Acc:HGNC:47830]"}, {"versioned_ensembl_gene_id":"ENSG00000264773.1","gene_symbol":"MIR4420","gene_name":"microRNA 4420 [Source:HGNC Symbol;Acc:HGNC:41772]","synonyms":"hsa-mir-4420","biotype":"miRNA","ncbi_id":"100616164","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30739156,"end":30739232,"strand":-1,"description":"microRNA 4420 [Source:HGNC Symbol;Acc:HGNC:41772]"}, {"versioned_ensembl_gene_id":"ENSG00000277119.1","gene_symbol":"WT1-AS_8","gene_name":"WT1 antisense RNA conserved region 8 [Source:RFAM;Acc:RF02210]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32440109,"end":32440383,"strand":1,"description":"WT1 antisense RNA conserved region 8 [Source:RFAM;Acc:RF02210]"}, {"versioned_ensembl_gene_id":"ENSG00000240481.3","gene_symbol":"RN7SL38P","gene_name":"RNA, 7SL, cytoplasmic 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46054]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480932","summary":null,"start":24706788,"end":24707083,"strand":1,"description":"RNA, 7SL, cytoplasmic 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46054]"}, {"versioned_ensembl_gene_id":"ENSG00000201518.1","gene_symbol":"RNA5SP513","gene_name":"RNA, 5S ribosomal pseudogene 513 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201032.1","gene_symbol":"RNU6-704P","gene_name":"RNA, U6 small nuclear 704, pseudogene [Source:HGNC Symbol;Acc:HGNC:47667]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479877","summary":null,"start":200933345,"end":200933447,"strand":-1,"description":"RNA, U6 small nuclear 704, pseudogene [Source:HGNC Symbol;Acc:HGNC:47667]"}, {"versioned_ensembl_gene_id":"ENSG00000212276.1","gene_symbol":"RNA5SP292","gene_name":"RNA, 5S ribosomal pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:43192]","synonyms":"RN5S292","biotype":"rRNA","ncbi_id":"100873545","summary":null,"start":106843749,"end":106843866,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:43192]"}, {"versioned_ensembl_gene_id":"ENSG00000221500.1","gene_symbol":"SNORD100","gene_name":"small nucleolar RNA, C/D box 100 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000276363.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000253089.1","gene_symbol":"RNU1-104P","gene_name":"RNA, U1 small nuclear 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:48446]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480184","summary":null,"start":127321355,"end":127321529,"strand":1,"description":"RNA, U1 small nuclear 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:48446]"}, {"versioned_ensembl_gene_id":"ENSG00000239040.1","gene_symbol":"Y_RNA","gene_name":"Y RNA 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polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145994784,"end":145994860,"strand":-1,"description":"microRNA 888 [Source:HGNC Symbol;Acc:HGNC:33648]"}, {"versioned_ensembl_gene_id":"ENSG00000208013.3","gene_symbol":"MIR652","gene_name":"microRNA 652 [Source:HGNC Symbol;Acc:HGNC:32908]","synonyms":"MIRN652,hsa-mir-652","biotype":"miRNA","ncbi_id":"724022","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110055329,"end":110055426,"strand":1,"description":"microRNA 652 [Source:HGNC Symbol;Acc:HGNC:32908]"}, {"versioned_ensembl_gene_id":"ENSG00000207169.1","gene_symbol":"RNU6-24P","gene_name":"RNA, U6 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:34268]","synonyms":"RNU6-24","biotype":"snRNA","ncbi_id":"106480707","summary":null,"start":76337316,"end":76337422,"strand":1,"description":"RNA, U6 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:34268]"}, {"versioned_ensembl_gene_id":"ENSG00000277888.1","gene_symbol":"MIR6846","gene_name":"microRNA 6846 [Source:HGNC Symbol;Acc:HGNC:50026]","synonyms":"hsa-mir-6846","biotype":"miRNA","ncbi_id":"102465509","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144057321,"end":144057380,"strand":-1,"description":"microRNA 6846 [Source:HGNC Symbol;Acc:HGNC:50026]"}, {"versioned_ensembl_gene_id":"ENSG00000221436.1","gene_symbol":"MIR548F3","gene_name":"microRNA 548f-3 [Source:HGNC Symbol;Acc:HGNC:35307]","synonyms":"MIRN548F3,hsa-mir-548f-3","biotype":"miRNA","ncbi_id":"100302159","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110513829,"end":110513915,"strand":-1,"description":"microRNA 548f-3 [Source:HGNC Symbol;Acc:HGNC:35307]"}, {"versioned_ensembl_gene_id":"ENSG00000222714.1","gene_symbol":"RN7SKP38","gene_name":"RNA, 7SK small nuclear pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45762]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479112","summary":null,"start":218500729,"end":218501037,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45762]"}, {"versioned_ensembl_gene_id":"ENSG00000201003.1","gene_symbol":"SNORA58","gene_name":"Small nucleolar RNA SNORA58 [Source:RFAM;Acc:RF00418]","synonyms":"SNORA58B,ACA58","biotype":"snoRNA","ncbi_id":"677836","summary":null,"start":53771018,"end":53771153,"strand":-1,"description":"Small nucleolar RNA SNORA58 [Source:RFAM;Acc:RF00418]"}, {"versioned_ensembl_gene_id":"ENSG00000284421.1","gene_symbol":"MIR7110","gene_name":"microRNA 7110 [Source:HGNC Symbol;Acc:HGNC:50024]","synonyms":"hsa-mir-7110","biotype":"miRNA","ncbi_id":"102465667","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123161794,"end":123161879,"strand":1,"description":"microRNA 7110 [Source:HGNC Symbol;Acc:HGNC:50024]"}, {"versioned_ensembl_gene_id":"ENSG00000252942.1","gene_symbol":"RNA5SP290","gene_name":"RNA, 5S ribosomal pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:43190]","synonyms":"RN5S290","biotype":"rRNA","ncbi_id":"100873543","summary":null,"start":99145840,"end":99145966,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:43190]"}, {"versioned_ensembl_gene_id":"ENSG00000240663.3","gene_symbol":"RN7SL310P","gene_name":"RNA, 7SL, cytoplasmic 310, pseudogene [Source:HGNC Symbol;Acc:HGNC:46326]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479336","summary":null,"start":50206998,"end":50207278,"strand":-1,"description":"RNA, 7SL, cytoplasmic 310, pseudogene [Source:HGNC Symbol;Acc:HGNC:46326]"}, {"versioned_ensembl_gene_id":"ENSG00000253023.1","gene_symbol":"RNU7-156P","gene_name":"RNA, U7 small nuclear 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:45690]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479083","summary":null,"start":143542514,"end":143542587,"strand":-1,"description":"RNA, U7 small nuclear 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:45690]"}, {"versioned_ensembl_gene_id":"ENSG00000278775.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8433085,"end":8433174,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000252890.1","gene_symbol":"RNU6-699P","gene_name":"RNA, U6 small nuclear 699, pseudogene [Source:HGNC Symbol;Acc:HGNC:47662]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479875","summary":null,"start":66897262,"end":66897371,"strand":1,"description":"RNA, U6 small nuclear 699, pseudogene [Source:HGNC Symbol;Acc:HGNC:47662]"}, {"versioned_ensembl_gene_id":"ENSG00000199728.1","gene_symbol":"RNU6-655P","gene_name":"RNA, U6 small nuclear 655, pseudogene [Source:HGNC Symbol;Acc:HGNC:47618]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479856","summary":null,"start":78036739,"end":78036845,"strand":1,"description":"RNA, U6 small nuclear 655, pseudogene [Source:HGNC Symbol;Acc:HGNC:47618]"}, {"versioned_ensembl_gene_id":"ENSG00000265193.1","gene_symbol":"MIR3923","gene_name":"microRNA 3923 [Source:HGNC Symbol;Acc:HGNC:38978]","synonyms":"hsa-mir-3923","biotype":"miRNA","ncbi_id":"100500877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79507887,"end":79507969,"strand":1,"description":"microRNA 3923 [Source:HGNC Symbol;Acc:HGNC:38978]"}, {"versioned_ensembl_gene_id":"ENSG00000278714.1","gene_symbol":"AL929561.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29063984,"end":29076511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266653.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32145516,"end":32145636,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000200665.1","gene_symbol":"RNU6-1188P","gene_name":"RNA, U6 small nuclear 1188, pseudogene [Source:HGNC Symbol;Acc:HGNC:48151]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480408","summary":null,"start":116082570,"end":116082676,"strand":1,"description":"RNA, U6 small nuclear 1188, pseudogene [Source:HGNC Symbol;Acc:HGNC:48151]"}, {"versioned_ensembl_gene_id":"ENSG00000200259.1","gene_symbol":"SNORD35A","gene_name":"small nucleolar RNA, C/D box 35A [Source:HGNC Symbol;Acc:HGNC:10162]","synonyms":"RNU35,U35,RNU35A","biotype":"snoRNA","ncbi_id":"26816","summary":null,"start":49491175,"end":49491260,"strand":1,"description":"small nucleolar RNA, C/D box 35A [Source:HGNC Symbol;Acc:HGNC:10162]"}, {"versioned_ensembl_gene_id":"ENSG00000207997.1","gene_symbol":"MIR644A","gene_name":"microRNA 644a [Source:HGNC Symbol;Acc:HGNC:32900]","synonyms":"MIRN644,MIR644,hsa-mir-644","biotype":"miRNA","ncbi_id":"693229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34466325,"end":34466418,"strand":1,"description":"microRNA 644a [Source:HGNC Symbol;Acc:HGNC:32900]"}, {"versioned_ensembl_gene_id":"ENSG00000201321.1","gene_symbol":"RNA5S9","gene_name":"RNA, 5S ribosomal 9 [Source:HGNC Symbol;Acc:HGNC:34370]","synonyms":"RN5S9","biotype":"rRNA","ncbi_id":"100169760","summary":null,"start":228628148,"end":228628266,"strand":-1,"description":"RNA, 5S ribosomal 9 [Source:HGNC Symbol;Acc:HGNC:34370]"}, {"versioned_ensembl_gene_id":"ENSG00000274721.1","gene_symbol":"SPRY4-IT1_2","gene_name":"SPRY4-IT1 conserved region 2 [Source:RFAM;Acc:RF02039]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":142318047,"end":142318167,"strand":1,"description":"SPRY4-IT1 conserved region 2 [Source:RFAM;Acc:RF02039]"}, {"versioned_ensembl_gene_id":"ENSG00000252423.1","gene_symbol":"RNU6-229P","gene_name":"RNA, U6 small nuclear 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:47192]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481250","summary":null,"start":69401202,"end":69401303,"strand":-1,"description":"RNA, U6 small nuclear 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:47192]"}, {"versioned_ensembl_gene_id":"ENSG00000263776.1","gene_symbol":"SNORA4","gene_name":"small nucleolar RNA, H/ACA box 4 [Source:HGNC Symbol;Acc:HGNC:32587]","synonyms":"ACA4","biotype":"snoRNA","ncbi_id":"619568","summary":null,"start":186787612,"end":186787749,"strand":1,"description":"small nucleolar RNA, H/ACA box 4 [Source:HGNC Symbol;Acc:HGNC:32587]"}, {"versioned_ensembl_gene_id":"ENSG00000284362.1","gene_symbol":"MIR519A2","gene_name":"microRNA 519a-2 [Source:HGNC Symbol;Acc:HGNC:32132]","synonyms":"MIRN519A2,MIRN519A-2,hsa-mir-519a-2","biotype":"miRNA","ncbi_id":"574500","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53762344,"end":53762430,"strand":1,"description":"microRNA 519a-2 [Source:HGNC Symbol;Acc:HGNC:32132]"}, {"versioned_ensembl_gene_id":"ENSG00000200222.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64071807,"end":64072019,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000239175.1","gene_symbol":"RNU6-1218P","gene_name":"RNA, U6 small nuclear 1218, pseudogene [Source:HGNC Symbol;Acc:HGNC:48181]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480099","summary":null,"start":30043801,"end":30043908,"strand":-1,"description":"RNA, U6 small nuclear 1218, pseudogene [Source:HGNC Symbol;Acc:HGNC:48181]"}, {"versioned_ensembl_gene_id":"ENSG00000276263.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,amida,FB1,FB1,INO80F,INO80F","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000199764.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":115207894,"end":115207996,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238653.1","gene_symbol":"RNU7-62P","gene_name":"RNA, U7 small nuclear 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:34158]","synonyms":"U7.62","biotype":"snRNA","ncbi_id":"100151657","summary":null,"start":64384398,"end":64384459,"strand":-1,"description":"RNA, U7 small nuclear 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:34158]"}, {"versioned_ensembl_gene_id":"ENSG00000276641.1","gene_symbol":"MIR6769A","gene_name":"microRNA 6769a [Source:HGNC Symbol;Acc:HGNC:50079]","synonyms":"hsa-mir-6769a","biotype":"miRNA","ncbi_id":"102466731","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4671318,"end":4671390,"strand":1,"description":"microRNA 6769a [Source:HGNC Symbol;Acc:HGNC:50079]"}, {"versioned_ensembl_gene_id":"ENSG00000222608.1","gene_symbol":"RNA5SP504","gene_name":"RNA, 5S ribosomal pseudogene 504 [Source:HGNC Symbol;Acc:HGNC:43404]","synonyms":"RN5S504","biotype":"rRNA","ncbi_id":"100873555","summary":null,"start":52665231,"end":52665347,"strand":1,"description":"RNA, 5S ribosomal pseudogene 504 [Source:HGNC Symbol;Acc:HGNC:43404]"}, {"versioned_ensembl_gene_id":"ENSG00000223037.1","gene_symbol":"RNU6-284P","gene_name":"RNA, U6 small nuclear 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:47247]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481268","summary":null,"start":164620732,"end":164620837,"strand":1,"description":"RNA, U6 small nuclear 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:47247]"}, {"versioned_ensembl_gene_id":"ENSG00000259722.2","gene_symbol":"AC087465.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77204578,"end":77205100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276878.1","gene_symbol":"MIR6074","gene_name":"microRNA 6074 [Source:HGNC Symbol;Acc:HGNC:50060]","synonyms":"hsa-mir-6074","biotype":"miRNA","ncbi_id":"102464827","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66023620,"end":66023726,"strand":-1,"description":"microRNA 6074 [Source:HGNC Symbol;Acc:HGNC:50060]"}, {"versioned_ensembl_gene_id":"ENSG00000251774.1","gene_symbol":"RNU6-377P","gene_name":"RNA, U6 small nuclear 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:47340]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479733","summary":null,"start":12514706,"end":12514807,"strand":1,"description":"RNA, U6 small nuclear 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:47340]"}, {"versioned_ensembl_gene_id":"ENSG00000200814.1","gene_symbol":"RNU6-595P","gene_name":"RNA, U6 small nuclear 595, pseudogene [Source:HGNC Symbol;Acc:HGNC:47558]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479829","summary":null,"start":62334091,"end":62334197,"strand":-1,"description":"RNA, U6 small nuclear 595, pseudogene [Source:HGNC Symbol;Acc:HGNC:47558]"}, {"versioned_ensembl_gene_id":"ENSG00000200830.1","gene_symbol":"RN7SKP134","gene_name":"RNA, 7SK small nuclear pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:45858]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479154","summary":null,"start":14553702,"end":14553970,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:45858]"}, {"versioned_ensembl_gene_id":"ENSG00000263628.1","gene_symbol":"MIR3155A","gene_name":"microRNA 3155a [Source:HGNC Symbol;Acc:HGNC:38245]","synonyms":"MIR3155,hsa-mir-3155","biotype":"miRNA","ncbi_id":"100422989","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6152196,"end":6152277,"strand":1,"description":"microRNA 3155a [Source:HGNC Symbol;Acc:HGNC:38245]"}, {"versioned_ensembl_gene_id":"ENSG00000252627.1","gene_symbol":"RNU6-122P","gene_name":"RNA, U6 small nuclear 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:47085]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481876","summary":null,"start":123874459,"end":123874565,"strand":1,"description":"RNA, U6 small nuclear 122, pseudogene [Source:HGNC Symbol;Acc:HGNC:47085]"}, {"versioned_ensembl_gene_id":"ENSG00000222869.1","gene_symbol":"RNU6-565P","gene_name":"RNA, U6 small nuclear 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:47528]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481360","summary":null,"start":37351143,"end":37351242,"strand":1,"description":"RNA, U6 small nuclear 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:47528]"}, {"versioned_ensembl_gene_id":"ENSG00000242348.3","gene_symbol":"RN7SL561P","gene_name":"RNA, 7SL, cytoplasmic 561, pseudogene [Source:HGNC Symbol;Acc:HGNC:46577]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481075","summary":null,"start":1666360,"end":1666640,"strand":1,"description":"RNA, 7SL, cytoplasmic 561, pseudogene [Source:HGNC Symbol;Acc:HGNC:46577]"}, {"versioned_ensembl_gene_id":"ENSG00000222520.1","gene_symbol":"RNA5SP451","gene_name":"RNA, 5S ribosomal pseudogene 451 [Source:HGNC Symbol;Acc:HGNC:43351]","synonyms":"RN5S451","biotype":"rRNA","ncbi_id":"100873696","summary":null,"start":21928985,"end":21929094,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 451 [Source:HGNC Symbol;Acc:HGNC:43351]"}, {"versioned_ensembl_gene_id":"ENSG00000283666.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":29510635,"end":29510737,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277809.1","gene_symbol":"Six3os1_4","gene_name":"Six3os1 conserved region 4 [Source:RFAM;Acc:RF02249]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44935585,"end":44935908,"strand":1,"description":"Six3os1 conserved region 4 [Source:RFAM;Acc:RF02249]"}, {"versioned_ensembl_gene_id":"ENSG00000263598.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28915807,"end":28915906,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000276096.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":4756338,"end":4756633,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000278284.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":54782118,"end":54801011,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000202382.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85367585,"end":85367686,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276260.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000263358.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31527123,"end":31527198,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000251720.1","gene_symbol":"RNU7-123P","gene_name":"RNA, U7 small nuclear 123 pseudogene [Source:HGNC Symbol;Acc:HGNC:45657]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479071","summary":null,"start":63536711,"end":63536770,"strand":-1,"description":"RNA, U7 small nuclear 123 pseudogene [Source:HGNC Symbol;Acc:HGNC:45657]"}, {"versioned_ensembl_gene_id":"ENSG00000283081.1","gene_symbol":"AL590644.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17193232,"end":17201733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239003.1","gene_symbol":"RNU7-88P","gene_name":"RNA, U7 small nuclear 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:42617]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873843","summary":null,"start":59480070,"end":59480132,"strand":1,"description":"RNA, U7 small nuclear 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:42617]"}, {"versioned_ensembl_gene_id":"ENSG00000207466.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38950825,"end":38950925,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199938.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38565950,"end":38566055,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284547.1","gene_symbol":"MIR2861","gene_name":"microRNA 2861 [Source:HGNC Symbol;Acc:HGNC:38221]","synonyms":"hsa-mir-2861","biotype":"miRNA","ncbi_id":"100422910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of target mRNAs. This microRNA may play a role in osteoblast differentiation and a mutation in this gene is associated with osteoporosis. Altered expression of this microRNA has been observed in human cancers, with reduced expression seen in cervical cancer, while expression in papillary thyroid carcinoma (PTC) is increased. [provided by RefSeq, Mar 2017]","start":127785918,"end":127786007,"strand":1,"description":"microRNA 2861 [Source:HGNC Symbol;Acc:HGNC:38221]"}, {"versioned_ensembl_gene_id":"ENSG00000277677.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51858070,"end":51858352,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000258452.1","gene_symbol":"AC022404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80822524,"end":80822796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237174.7","gene_symbol":"AL445465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75357214,"end":75399300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283278.1","gene_symbol":"MIR3914-2","gene_name":"microRNA 3914-2 [Source:HGNC Symbol;Acc:HGNC:38975]","synonyms":"hsa-mir-3914-2","biotype":"miRNA","ncbi_id":"100500920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71307674,"end":71307768,"strand":1,"description":"microRNA 3914-2 [Source:HGNC Symbol;Acc:HGNC:38975]"}, {"versioned_ensembl_gene_id":"ENSG00000212615.1","gene_symbol":"SNORD58","gene_name":"Small nucleolar RNA SNORD58 [Source:RFAM;Acc:RF00151]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":45088243,"end":45088308,"strand":1,"description":"Small nucleolar RNA SNORD58 [Source:RFAM;Acc:RF00151]"}, {"versioned_ensembl_gene_id":"ENSG00000201470.1","gene_symbol":"RNY4P7","gene_name":"RNA, Ro-associated Y4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34056]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100169850","summary":null,"start":127798903,"end":127798998,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34056]"}, {"versioned_ensembl_gene_id":"ENSG00000202100.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32463374,"end":32463482,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222276.1","gene_symbol":"RNU2-33P","gene_name":"RNA, U2 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48526]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480211","summary":null,"start":96384624,"end":96384815,"strand":1,"description":"RNA, U2 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48526]"}, {"versioned_ensembl_gene_id":"ENSG00000221042.1","gene_symbol":"CPEB3_ribozyme","gene_name":"Mammalian CPEB3 ribozyme [Source:RFAM;Acc:RF00622]","synonyms":null,"biotype":"ribozyme","ncbi_id":null,"summary":null,"start":92204229,"end":92204306,"strand":-1,"description":"Mammalian CPEB3 ribozyme [Source:RFAM;Acc:RF00622]"}, {"versioned_ensembl_gene_id":"ENSG00000274894.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000199785.1","gene_symbol":"SNORA52","gene_name":"small nucleolar RNA, H/ACA box 52 [Source:HGNC Symbol;Acc:HGNC:32645]","synonyms":"ACA52","biotype":"snoRNA","ncbi_id":"619565","summary":null,"start":811681,"end":811814,"strand":1,"description":"small nucleolar RNA, H/ACA box 52 [Source:HGNC Symbol;Acc:HGNC:32645]"}, {"versioned_ensembl_gene_id":"ENSG00000206727.1","gene_symbol":"SNORD116-9","gene_name":"small nucleolar RNA, C/D box 116-9 [Source:HGNC Symbol;Acc:HGNC:33075]","synonyms":"HBII-85-9","biotype":"snoRNA","ncbi_id":"100033421","summary":null,"start":25073107,"end":25073201,"strand":1,"description":"small nucleolar RNA, C/D box 116-9 [Source:HGNC Symbol;Acc:HGNC:33075]"}, {"versioned_ensembl_gene_id":"ENSG00000276123.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":194658376,"end":194658675,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207365.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93021606,"end":93021712,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276161.1","gene_symbol":"SNORA17B","gene_name":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]","synonyms":"SNORA43,ACA43,SNORA43,ACA43","biotype":"snoRNA","ncbi_id":"677824","summary":null,"start":136726105,"end":136726234,"strand":-1,"description":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]"}, {"versioned_ensembl_gene_id":"ENSG00000283665.1","gene_symbol":"MIR3974","gene_name":"microRNA 3974 [Source:HGNC Symbol;Acc:HGNC:41672]","synonyms":"hsa-mir-3974","biotype":"miRNA","ncbi_id":"100616279","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17673299,"end":17673394,"strand":1,"description":"microRNA 3974 [Source:HGNC Symbol;Acc:HGNC:41672]"}, {"versioned_ensembl_gene_id":"ENSG00000221650.1","gene_symbol":"MIR1267","gene_name":"microRNA 1267 [Source:HGNC Symbol;Acc:HGNC:35335]","synonyms":"hsa-mir-1267,MIRN1267","biotype":"miRNA","ncbi_id":"100302286","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":107531171,"end":107531248,"strand":-1,"description":"microRNA 1267 [Source:HGNC Symbol;Acc:HGNC:35335]"}, {"versioned_ensembl_gene_id":"ENSG00000199913.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73095357,"end":73095458,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000198997.2","gene_symbol":"MIR107","gene_name":"microRNA 107 [Source:HGNC Symbol;Acc:HGNC:31496]","synonyms":"MIRN107,hsa-mir-107","biotype":"miRNA","ncbi_id":"406901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89592747,"end":89592827,"strand":-1,"description":"microRNA 107 [Source:HGNC Symbol;Acc:HGNC:31496]"}, {"versioned_ensembl_gene_id":"ENSG00000201365.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66653469,"end":66653576,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206900.1","gene_symbol":"RNU6-98P","gene_name":"RNA, U6 small nuclear 98, pseudogene [Source:HGNC Symbol;Acc:HGNC:47061]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479609","summary":null,"start":132580117,"end":132580223,"strand":-1,"description":"RNA, U6 small nuclear 98, pseudogene [Source:HGNC Symbol;Acc:HGNC:47061]"}, {"versioned_ensembl_gene_id":"ENSG00000262000.1","gene_symbol":"AC120024.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80515215,"end":80515389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263476.1","gene_symbol":"MIR3156-1","gene_name":"microRNA 3156-1 [Source:HGNC Symbol;Acc:HGNC:38241]","synonyms":"hsa-mir-3156-1","biotype":"miRNA","ncbi_id":"100422988","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45164014,"end":45164088,"strand":1,"description":"microRNA 3156-1 [Source:HGNC Symbol;Acc:HGNC:38241]"}, {"versioned_ensembl_gene_id":"ENSG00000200972.1","gene_symbol":"RNU5A-8P","gene_name":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873838","summary":null,"start":210374154,"end":210374267,"strand":-1,"description":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]"}, {"versioned_ensembl_gene_id":"ENSG00000212475.1","gene_symbol":"RNU6-400P","gene_name":"RNA, U6 small nuclear 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:47363]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481304","summary":null,"start":33576095,"end":33576200,"strand":1,"description":"RNA, U6 small nuclear 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:47363]"}, {"versioned_ensembl_gene_id":"ENSG00000201690.1","gene_symbol":"RNY1P2","gene_name":"RNA, Ro-associated Y1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42479]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862666","summary":null,"start":102016953,"end":102017069,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42479]"}, {"versioned_ensembl_gene_id":"ENSG00000212565.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":48880840,"end":48880967,"strand":1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000252719.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":139909904,"end":139910034,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000223271.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66348276,"end":66348375,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277167.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30763377,"end":30763613,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222329.1","gene_symbol":"RNU6-1076P","gene_name":"RNA, U6 small nuclear 1076, pseudogene [Source:HGNC Symbol;Acc:HGNC:48039]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480038","summary":null,"start":223158,"end":223261,"strand":-1,"description":"RNA, U6 small nuclear 1076, pseudogene [Source:HGNC Symbol;Acc:HGNC:48039]"}, {"versioned_ensembl_gene_id":"ENSG00000252952.1","gene_symbol":"RNU6-58P","gene_name":"RNA, U6 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:42548]","synonyms":"RNU6-58","biotype":"snRNA","ncbi_id":"100873766","summary":null,"start":23217432,"end":23217534,"strand":-1,"description":"RNA, U6 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:42548]"}, {"versioned_ensembl_gene_id":"ENSG00000200855.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108084913,"end":108085014,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201992.1","gene_symbol":"SNORD115-35","gene_name":"small nucleolar RNA, C/D box 115-35 [Source:HGNC Symbol;Acc:HGNC:33054]","synonyms":"HBII-52-35","biotype":"snoRNA","ncbi_id":"100033809","summary":null,"start":25234247,"end":25234328,"strand":1,"description":"small nucleolar RNA, C/D box 115-35 [Source:HGNC Symbol;Acc:HGNC:33054]"}, {"versioned_ensembl_gene_id":"ENSG00000277139.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":69530371,"end":69530475,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000222895.1","gene_symbol":"RNU6-1133P","gene_name":"RNA, U6 small nuclear 1133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48096]","synonyms":"RNU6-186P","biotype":"snRNA","ncbi_id":"106481537","summary":null,"start":31083010,"end":31083109,"strand":1,"description":"RNA, U6 small nuclear 1133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48096]"}, {"versioned_ensembl_gene_id":"ENSG00000202195.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52297995,"end":52298096,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280505.1","gene_symbol":"AC097369.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72583719,"end":72583884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284459.1","gene_symbol":"MIR24-1","gene_name":"microRNA 24-1 [Source:HGNC Symbol;Acc:HGNC:31607]","synonyms":"MIRN24-1,hsa-mir-24-1","biotype":"miRNA","ncbi_id":"407012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95086021,"end":95086088,"strand":1,"description":"microRNA 24-1 [Source:HGNC Symbol;Acc:HGNC:31607]"}, {"versioned_ensembl_gene_id":"ENSG00000207698.1","gene_symbol":"MIR32","gene_name":"microRNA 32 [Source:HGNC Symbol;Acc:HGNC:31631]","synonyms":"MIRN32,hsa-mir-32","biotype":"miRNA","ncbi_id":"407036","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109046229,"end":109046298,"strand":-1,"description":"microRNA 32 [Source:HGNC Symbol;Acc:HGNC:31631]"}, {"versioned_ensembl_gene_id":"ENSG00000216064.1","gene_symbol":"MIR891B","gene_name":"microRNA 891b [Source:HGNC Symbol;Acc:HGNC:33645]","synonyms":"MIRN891B,hsa-mir-891b","biotype":"miRNA","ncbi_id":"100126304","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":146001053,"end":146001131,"strand":-1,"description":"microRNA 891b [Source:HGNC Symbol;Acc:HGNC:33645]"}, {"versioned_ensembl_gene_id":"ENSG00000225944.1","gene_symbol":"RIOK3P1","gene_name":"RIO kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122145","summary":null,"start":74828553,"end":74830080,"strand":1,"description":"RIO kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39714]"}, {"versioned_ensembl_gene_id":"ENSG00000265669.1","gene_symbol":"MIR548AJ1","gene_name":"microRNA 548aj-1 [Source:HGNC Symbol;Acc:HGNC:41884]","synonyms":"hsa-mir-548aj-1","biotype":"miRNA","ncbi_id":"100616191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132115192,"end":132115263,"strand":-1,"description":"microRNA 548aj-1 [Source:HGNC Symbol;Acc:HGNC:41884]"}, {"versioned_ensembl_gene_id":"ENSG00000265657.1","gene_symbol":"MIR3151","gene_name":"microRNA 3151 [Source:HGNC Symbol;Acc:HGNC:38266]","synonyms":"hsa-mir-3151","biotype":"miRNA","ncbi_id":"100422992","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103154614,"end":103154689,"strand":1,"description":"microRNA 3151 [Source:HGNC Symbol;Acc:HGNC:38266]"}, {"versioned_ensembl_gene_id":"ENSG00000276824.1","gene_symbol":"MIR7159","gene_name":"microRNA 7159 [Source:HGNC Symbol;Acc:HGNC:49978]","synonyms":"hsa-mir-7159","biotype":"miRNA","ncbi_id":"102466816","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33899135,"end":33899200,"strand":1,"description":"microRNA 7159 [Source:HGNC Symbol;Acc:HGNC:49978]"}, {"versioned_ensembl_gene_id":"ENSG00000221398.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"U107,SNORA11A","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":34456110,"end":34456237,"strand":-1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000212490.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":52748137,"end":52748259,"strand":1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000238685.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":12297197,"end":12297323,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000223092.1","gene_symbol":"RNA5SP115","gene_name":"RNA, 5S ribosomal pseudogene 115 [Source:HGNC Symbol;Acc:HGNC:42913]","synonyms":"RN5S115","biotype":"rRNA","ncbi_id":"100873385","summary":null,"start":200849038,"end":200849144,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 115 [Source:HGNC Symbol;Acc:HGNC:42913]"}, {"versioned_ensembl_gene_id":"ENSG00000252328.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35097560,"end":35097657,"strand":-1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000277250.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128673681,"end":128674021,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238778.1","gene_symbol":"RNU7-80P","gene_name":"RNA, U7 small nuclear 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:34176]","synonyms":"U7.80","biotype":"snRNA","ncbi_id":"100151677","summary":null,"start":67772593,"end":67772653,"strand":-1,"description":"RNA, U7 small nuclear 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:34176]"}, {"versioned_ensembl_gene_id":"ENSG00000283225.1","gene_symbol":"MIR3199-2","gene_name":"microRNA 3199-2 [Source:HGNC Symbol;Acc:HGNC:38205]","synonyms":"hsa-mir-3199-2","biotype":"miRNA","ncbi_id":"100422998","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27920526,"end":27920611,"strand":1,"description":"microRNA 3199-2 [Source:HGNC Symbol;Acc:HGNC:38205]"}, {"versioned_ensembl_gene_id":"ENSG00000284175.1","gene_symbol":"MIR4763","gene_name":"microRNA 4763 [Source:HGNC Symbol;Acc:HGNC:41677]","synonyms":"hsa-mir-4763","biotype":"miRNA","ncbi_id":"100616143","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46113566,"end":46113657,"strand":1,"description":"microRNA 4763 [Source:HGNC Symbol;Acc:HGNC:41677]"}, {"versioned_ensembl_gene_id":"ENSG00000224943.1","gene_symbol":"AL663023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159466321,"end":159483376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228210.1","gene_symbol":"AL121916.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4590993,"end":4591300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251799.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56818218,"end":56818314,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264802.1","gene_symbol":"MIR5191","gene_name":"microRNA 5191 [Source:HGNC Symbol;Acc:HGNC:43497]","synonyms":"hsa-mir-5191","biotype":"miRNA","ncbi_id":"100847050","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":201719508,"end":201719627,"strand":1,"description":"microRNA 5191 [Source:HGNC Symbol;Acc:HGNC:43497]"}, {"versioned_ensembl_gene_id":"ENSG00000207708.1","gene_symbol":"MIR141","gene_name":"microRNA 141 [Source:HGNC Symbol;Acc:HGNC:31528]","synonyms":"MIRN141,hsa-mir-141","biotype":"miRNA","ncbi_id":"406933","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6964097,"end":6964191,"strand":1,"description":"microRNA 141 [Source:HGNC Symbol;Acc:HGNC:31528]"}, {"versioned_ensembl_gene_id":"ENSG00000200075.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"ACA25,SNORA25A","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":129868590,"end":129868716,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000244618.3","gene_symbol":"RN7SL334P","gene_name":"RNA, 7SL, cytoplasmic 334, pseudogene [Source:HGNC Symbol;Acc:HGNC:46350]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480502","summary":null,"start":25031009,"end":25031287,"strand":-1,"description":"RNA, 7SL, cytoplasmic 334, pseudogene [Source:HGNC Symbol;Acc:HGNC:46350]"}, {"versioned_ensembl_gene_id":"ENSG00000200867.1","gene_symbol":"RN7SKP36","gene_name":"RNA, 7SK small nuclear pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45760]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480458","summary":null,"start":7112088,"end":7112399,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45760]"}, {"versioned_ensembl_gene_id":"ENSG00000221464.1","gene_symbol":"MIR1271","gene_name":"microRNA 1271 [Source:HGNC Symbol;Acc:HGNC:35252]","synonyms":"MIRN1271,hsa-mir-1271","biotype":"miRNA","ncbi_id":"100302203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176367946,"end":176368031,"strand":1,"description":"microRNA 1271 [Source:HGNC Symbol;Acc:HGNC:35252]"}, {"versioned_ensembl_gene_id":"ENSG00000265691.1","gene_symbol":"MIR4460","gene_name":"microRNA 4460 [Source:HGNC Symbol;Acc:HGNC:41795]","synonyms":"hsa-mir-4460","biotype":"miRNA","ncbi_id":"100616325","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129397062,"end":129397147,"strand":-1,"description":"microRNA 4460 [Source:HGNC Symbol;Acc:HGNC:41795]"}, {"versioned_ensembl_gene_id":"ENSG00000284182.1","gene_symbol":"MIR143","gene_name":"microRNA 143 [Source:HGNC Symbol;Acc:HGNC:31530]","synonyms":"MIRN143,hsa-mir-143","biotype":"miRNA","ncbi_id":"406935","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149428918,"end":149429023,"strand":1,"description":"microRNA 143 [Source:HGNC Symbol;Acc:HGNC:31530]"}, {"versioned_ensembl_gene_id":"ENSG00000207039.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153785720,"end":153785821,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199520.1","gene_symbol":"RNU6-386P","gene_name":"RNA, U6 small nuclear 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:47349]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481300","summary":null,"start":77092057,"end":77092163,"strand":1,"description":"RNA, U6 small nuclear 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:47349]"}, {"versioned_ensembl_gene_id":"ENSG00000202438.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130573996,"end":130574112,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207090.1","gene_symbol":"RNU6-517P","gene_name":"RNA, U6 small nuclear 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:47480]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479795","summary":null,"start":121194948,"end":121195057,"strand":-1,"description":"RNA, U6 small nuclear 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:47480]"}, {"versioned_ensembl_gene_id":"ENSG00000201999.1","gene_symbol":"RNA5SP428","gene_name":"RNA, 5S ribosomal pseudogene 428 [Source:HGNC Symbol;Acc:HGNC:43328]","synonyms":"RN5S428","biotype":"rRNA","ncbi_id":"100873679","summary":null,"start":66301809,"end":66301940,"strand":1,"description":"RNA, 5S ribosomal pseudogene 428 [Source:HGNC Symbol;Acc:HGNC:43328]"}, {"versioned_ensembl_gene_id":"ENSG00000253676.1","gene_symbol":"TAGLN2P1","gene_name":"transgelin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418887","summary":null,"start":106697427,"end":106698013,"strand":-1,"description":"transgelin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21739]"}, {"versioned_ensembl_gene_id":"ENSG00000238282.1","gene_symbol":"AL121781.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4475638,"end":4525200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279706.1","gene_symbol":"AL353608.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68250469,"end":68251656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284010.1","gene_symbol":"MIR675","gene_name":"microRNA 675 [Source:HGNC Symbol;Acc:HGNC:33351]","synonyms":"MIRN675,hsa-mir-675","biotype":"miRNA","ncbi_id":"100033819","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1996759,"end":1996831,"strand":-1,"description":"microRNA 675 [Source:HGNC Symbol;Acc:HGNC:33351]"}, {"versioned_ensembl_gene_id":"ENSG00000281393.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133337876,"end":133337972,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202609.4","gene_symbol":"MIR488","gene_name":"microRNA 488 [Source:HGNC Symbol;Acc:HGNC:32073]","synonyms":"MIRN488,hsa-mir-488","biotype":"miRNA","ncbi_id":"574441","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177029363,"end":177029445,"strand":-1,"description":"microRNA 488 [Source:HGNC Symbol;Acc:HGNC:32073]"}, {"versioned_ensembl_gene_id":"ENSG00000221669.1","gene_symbol":"MIR548N","gene_name":"microRNA 548n [Source:HGNC Symbol;Acc:HGNC:35330]","synonyms":"MIRN548N,hsa-mir-548n","biotype":"miRNA","ncbi_id":"100302152","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34940760,"end":34940834,"strand":-1,"description":"microRNA 548n [Source:HGNC Symbol;Acc:HGNC:35330]"}, {"versioned_ensembl_gene_id":"ENSG00000283921.1","gene_symbol":"MIR1302-9","gene_name":"microRNA 1302-9 [Source:HGNC Symbol;Acc:HGNC:38218]","synonyms":"hsa-mir-1302-9","biotype":"miRNA","ncbi_id":"100422831","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30144,"end":30281,"strand":1,"description":"microRNA 1302-9 [Source:HGNC Symbol;Acc:HGNC:38218]"}, {"versioned_ensembl_gene_id":"ENSG00000198983.1","gene_symbol":"MIR449A","gene_name":"microRNA 449a [Source:HGNC Symbol;Acc:HGNC:27645]","synonyms":"MIRN449A,MIRN449,hsa-mir-449a,hsa-mir-449","biotype":"miRNA","ncbi_id":"554213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55170532,"end":55170622,"strand":-1,"description":"microRNA 449a [Source:HGNC Symbol;Acc:HGNC:27645]"}, {"versioned_ensembl_gene_id":"ENSG00000277073.1","gene_symbol":"MIR6131","gene_name":"microRNA 6131 [Source:HGNC Symbol;Acc:HGNC:49929]","synonyms":"hsa-mir-6131","biotype":"miRNA","ncbi_id":"102465138","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10478037,"end":10478145,"strand":1,"description":"microRNA 6131 [Source:HGNC Symbol;Acc:HGNC:49929]"}, {"versioned_ensembl_gene_id":"ENSG00000174231.16","gene_symbol":"PRPF8","gene_name":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]","synonyms":"RP13,PRPC8,Prp8,hPrp8,SNRNP220","biotype":"protein_coding","ncbi_id":"10594","summary":"Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2- and U12-dependent spliceosomes, and found to be essential for the catalytic step II in pre-mRNA splicing process. It contains several WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":1650629,"end":1684882,"strand":-1,"description":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]"}, {"versioned_ensembl_gene_id":"ENSG00000284561.1","gene_symbol":"MIR4788","gene_name":"microRNA 4788 [Source:HGNC Symbol;Acc:HGNC:41676]","synonyms":"hsa-mir-4788","biotype":"miRNA","ncbi_id":"100616281","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134437827,"end":134437906,"strand":1,"description":"microRNA 4788 [Source:HGNC Symbol;Acc:HGNC:41676]"}, {"versioned_ensembl_gene_id":"ENSG00000207650.1","gene_symbol":"MIR570","gene_name":"microRNA 570 [Source:HGNC Symbol;Acc:HGNC:32826]","synonyms":"MIRN570,hsa-mir-570","biotype":"miRNA","ncbi_id":"693155","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":195699401,"end":195699497,"strand":1,"description":"microRNA 570 [Source:HGNC Symbol;Acc:HGNC:32826]"}, {"versioned_ensembl_gene_id":"ENSG00000283203.1","gene_symbol":"MIR1246","gene_name":"microRNA 1246 [Source:HGNC Symbol;Acc:HGNC:35312]","synonyms":"MIRN1246,hsa-mir-1246","biotype":"miRNA","ncbi_id":"100302142","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176600980,"end":176601052,"strand":-1,"description":"microRNA 1246 [Source:HGNC Symbol;Acc:HGNC:35312]"}, {"versioned_ensembl_gene_id":"ENSG00000201421.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185251313,"end":185251411,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238943.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8592476,"end":8592585,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275068.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":64082429,"end":64082534,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201371.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27722284,"end":27722392,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252945.1","gene_symbol":"snoU83B","gene_name":"Small nucleolar RNA U83B [Source:RFAM;Acc:RF00593]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":50844625,"end":50844712,"strand":1,"description":"Small nucleolar RNA U83B [Source:RFAM;Acc:RF00593]"}, {"versioned_ensembl_gene_id":"ENSG00000216056.1","gene_symbol":"MIR891A","gene_name":"microRNA 891a [Source:HGNC Symbol;Acc:HGNC:33635]","synonyms":"MIRN891A,hsa-mir-891a","biotype":"miRNA","ncbi_id":"100126341","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":146027794,"end":146027872,"strand":-1,"description":"microRNA 891a [Source:HGNC Symbol;Acc:HGNC:33635]"}, {"versioned_ensembl_gene_id":"ENSG00000252431.1","gene_symbol":"RNU6-1247P","gene_name":"RNA, U6 small nuclear 1247, pseudogene [Source:HGNC Symbol;Acc:HGNC:48210]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481574","summary":null,"start":151280515,"end":151280612,"strand":-1,"description":"RNA, U6 small nuclear 1247, pseudogene [Source:HGNC Symbol;Acc:HGNC:48210]"}, {"versioned_ensembl_gene_id":"ENSG00000283941.1","gene_symbol":"MIR600","gene_name":"microRNA 600 [Source:HGNC Symbol;Acc:HGNC:32856]","synonyms":"MIRN600,hsa-mir-600","biotype":"miRNA","ncbi_id":"693185","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123111546,"end":123111643,"strand":-1,"description":"microRNA 600 [Source:HGNC Symbol;Acc:HGNC:32856]"}, {"versioned_ensembl_gene_id":"ENSG00000137752.23","gene_symbol":"CASP1","gene_name":"caspase 1 [Source:HGNC Symbol;Acc:HGNC:1499]","synonyms":"IL1BC,ICE","biotype":"protein_coding","ncbi_id":"834","summary":"This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce 2 subunits, large and small, that dimerize to form the active enzyme. This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing. This gene has been shown to induce cell apoptosis and may function in various developmental stages. Studies of a similar gene in mouse suggest a role in the pathogenesis of Huntington disease. Alternative splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2012]","start":105025443,"end":105035250,"strand":-1,"description":"caspase 1 [Source:HGNC Symbol;Acc:HGNC:1499]"}, {"versioned_ensembl_gene_id":"ENSG00000207651.1","gene_symbol":"MIR28","gene_name":"microRNA 28 [Source:HGNC Symbol;Acc:HGNC:31615]","synonyms":"MIRN28,hsa-mir-28","biotype":"miRNA","ncbi_id":"407020","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188688781,"end":188688866,"strand":1,"description":"microRNA 28 [Source:HGNC Symbol;Acc:HGNC:31615]"}, {"versioned_ensembl_gene_id":"ENSG00000265141.2","gene_symbol":"RN7SL451P","gene_name":"RNA, 7SL, cytoplasmic 451, pseudogene [Source:HGNC Symbol;Acc:HGNC:46467]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480377","summary":null,"start":8979576,"end":8979874,"strand":-1,"description":"RNA, 7SL, cytoplasmic 451, pseudogene [Source:HGNC Symbol;Acc:HGNC:46467]"}, {"versioned_ensembl_gene_id":"ENSG00000200842.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62036833,"end":62036945,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222067.1","gene_symbol":"RNU4-86P","gene_name":"RNA, U4 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47022]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481199","summary":null,"start":126214260,"end":126214478,"strand":-1,"description":"RNA, U4 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47022]"}, {"versioned_ensembl_gene_id":"ENSG00000212306.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100638363,"end":100638457,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201584.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121040610,"end":121040710,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201315.1","gene_symbol":"RN7SKP227","gene_name":"RNA, 7SK small nuclear pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:45951]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481818","summary":null,"start":36685040,"end":36685369,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:45951]"}, {"versioned_ensembl_gene_id":"ENSG00000201394.1","gene_symbol":"RNA5SP140","gene_name":"RNA, 5S ribosomal pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:43040]","synonyms":"RN5S140","biotype":"rRNA","ncbi_id":"106478996","summary":null,"start":133710076,"end":133710167,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:43040]"}, {"versioned_ensembl_gene_id":"ENSG00000276311.1","gene_symbol":"MIR6511A3","gene_name":"microRNA 6511a-3 [Source:HGNC Symbol;Acc:HGNC:50265]","synonyms":"hsa-mir-6511a-3","biotype":"miRNA","ncbi_id":"102465683","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16368876,"end":16368942,"strand":1,"description":"microRNA 6511a-3 [Source:HGNC Symbol;Acc:HGNC:50265]"}, {"versioned_ensembl_gene_id":"ENSG00000206891.1","gene_symbol":"RNU6-217P","gene_name":"RNA, U6 small nuclear 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:47180]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481246","summary":null,"start":77811741,"end":77811844,"strand":-1,"description":"RNA, U6 small nuclear 217, pseudogene [Source:HGNC Symbol;Acc:HGNC:47180]"}, {"versioned_ensembl_gene_id":"ENSG00000276639.1","gene_symbol":"MIR7154","gene_name":"microRNA 7154 [Source:HGNC Symbol;Acc:HGNC:49972]","synonyms":"hsa-mir-7154","biotype":"miRNA","ncbi_id":"102465691","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45691704,"end":45691776,"strand":-1,"description":"microRNA 7154 [Source:HGNC Symbol;Acc:HGNC:49972]"}, {"versioned_ensembl_gene_id":"ENSG00000222268.1","gene_symbol":"RNA5SP425","gene_name":"RNA, 5S ribosomal pseudogene 425 [Source:HGNC Symbol;Acc:HGNC:43325]","synonyms":"RN5S425","biotype":"rRNA","ncbi_id":"100873676","summary":null,"start":47505432,"end":47505543,"strand":1,"description":"RNA, 5S ribosomal pseudogene 425 [Source:HGNC Symbol;Acc:HGNC:43325]"}, {"versioned_ensembl_gene_id":"ENSG00000207516.1","gene_symbol":"SNORA41B","gene_name":"small nucleolar RNA, H/ACA box 41B [Source:HGNC Symbol;Acc:HGNC:52206]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617005","summary":null,"start":45537250,"end":45537377,"strand":1,"description":"small nucleolar RNA, H/ACA box 41B [Source:HGNC Symbol;Acc:HGNC:52206]"}, {"versioned_ensembl_gene_id":"ENSG00000200495.1","gene_symbol":"RNU6-1205P","gene_name":"RNA, U6 small nuclear 1205, pseudogene [Source:HGNC Symbol;Acc:HGNC:48168]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480093","summary":null,"start":248912690,"end":248912795,"strand":-1,"description":"RNA, U6 small nuclear 1205, pseudogene [Source:HGNC Symbol;Acc:HGNC:48168]"}, {"versioned_ensembl_gene_id":"ENSG00000271907.1","gene_symbol":"SNORA35B","gene_name":"small nucleolar RNA, H/ACA box 35B [Source:HGNC Symbol;Acc:HGNC:52202]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617004","summary":null,"start":115126316,"end":115126444,"strand":-1,"description":"small nucleolar RNA, H/ACA box 35B [Source:HGNC Symbol;Acc:HGNC:52202]"}, {"versioned_ensembl_gene_id":"ENSG00000155959.10","gene_symbol":"VBP1","gene_name":"VHL binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12662]","synonyms":"PFDN3,PFD3","biotype":"protein_coding","ncbi_id":"7411","summary":"The protein encoded by this gene interacts with the Von Hippel-Lindau protein to form an intracellular complex. The encoded protein functions as a chaperone protein, and may play a role in the transport of the Von Hippel-Lindau protein from the perinuclear granules to the nucleus or cytoplasm. Alternative splicing and the use of alternate transcription start sites results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Jan 2015]","start":155197007,"end":155239817,"strand":1,"description":"VHL binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12662]"}, {"versioned_ensembl_gene_id":"ENSG00000283036.2","gene_symbol":"LINC01988","gene_name":"long intergenic non-protein coding RNA 1988 [Source:HGNC Symbol;Acc:HGNC:52820]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506319","summary":null,"start":44424134,"end":44429529,"strand":1,"description":"long intergenic non-protein coding RNA 1988 [Source:HGNC Symbol;Acc:HGNC:52820]"}, {"versioned_ensembl_gene_id":"ENSG00000133983.14","gene_symbol":"COX16","gene_name":"COX16, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:20213]","synonyms":"HSPC203,C14orf112","biotype":"protein_coding","ncbi_id":"51241","summary":null,"start":70325081,"end":70359731,"strand":-1,"description":"COX16, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:20213]"}, {"versioned_ensembl_gene_id":"ENSG00000144668.11","gene_symbol":"ITGA9","gene_name":"integrin subunit alpha 9 [Source:HGNC Symbol;Acc:HGNC:6145]","synonyms":"RLC,ITGA4L,ALPHA-RLC","biotype":"protein_coding","ncbi_id":"3680","summary":"This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane glycoproteins composed of an alpha chain and a beta chain that mediate cell-cell and cell-matrix adhesion. The protein encoded by this gene, when bound to the beta 1 chain, forms an integrin that is a receptor for VCAM1, cytotactin and osteopontin. Expression of this gene has been found to be upregulated in small cell lung cancers. [provided by RefSeq, Jul 2008]","start":37452115,"end":37823514,"strand":1,"description":"integrin subunit alpha 9 [Source:HGNC Symbol;Acc:HGNC:6145]"}, {"versioned_ensembl_gene_id":"ENSG00000127241.16","gene_symbol":"MASP1","gene_name":"mannan binding lectin serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:6901]","synonyms":"PRSS5,MASP,CRARF","biotype":"protein_coding","ncbi_id":"5648","summary":"This gene encodes a serine protease that functions as a component of the lectin pathway of complement activation. The complement pathway plays an essential role in the innate and adaptive immune response. The encoded protein is synthesized as a zymogen and is activated when it complexes with the pathogen recognition molecules of lectin pathway, the mannose-binding lectin and the ficolins. This protein is not directly involved in complement activation but may play a role as an amplifier of complement activation by cleaving complement C2 or by activating another complement serine protease, MASP-2. The encoded protein is also able to cleave fibrinogen and factor XIII and may may be involved in coagulation. A splice variant of this gene which lacks the serine protease domain functions as an inhibitor of the complement pathway. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":187217285,"end":187292022,"strand":-1,"description":"mannan binding lectin serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:6901]"}, {"versioned_ensembl_gene_id":"ENSG00000165458.13","gene_symbol":"INPPL1","gene_name":"inositol polyphosphate phosphatase like 1 [Source:HGNC Symbol;Acc:HGNC:6080]","synonyms":"SHIP2","biotype":"protein_coding","ncbi_id":"3636","summary":"The protein encoded by this gene is an SH2-containing 5'-inositol phosphatase that is involved in the regulation of insulin function. The encoded protein also plays a role in the regulation of epidermal growth factor receptor turnover and actin remodelling. Additionally, this gene supports metastatic growth in breast cancer and is a valuable biomarker for breast cancer. [provided by RefSeq, Jan 2009]","start":72223701,"end":72239105,"strand":1,"description":"inositol polyphosphate phosphatase like 1 [Source:HGNC Symbol;Acc:HGNC:6080]"}, {"versioned_ensembl_gene_id":"ENSG00000230660.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"Em:AB014087.1,FLJ31598,FLJ25550","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30335445,"end":30371782,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000227519.1","gene_symbol":"AL008719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31963357,"end":31970400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276885.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832710,"end":54847746,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000277691.4","gene_symbol":"GU182338.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54786460,"end":54798282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170827.9","gene_symbol":"CELP","gene_name":"carboxyl ester lipase pseudogene [Source:HGNC Symbol;Acc:HGNC:1849]","synonyms":"CELL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1057","summary":null,"start":133079900,"end":133087355,"strand":1,"description":"carboxyl ester lipase pseudogene [Source:HGNC Symbol;Acc:HGNC:1849]"}, {"versioned_ensembl_gene_id":"ENSG00000228663.1","gene_symbol":"PSMD10P1","gene_name":"proteasome 26S subunit, non-ATPase, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16602]","synonyms":"PSMD10P,dJ914P20.4","biotype":"processed_pseudogene","ncbi_id":"170541","summary":null,"start":50913731,"end":50914411,"strand":1,"description":"proteasome 26S subunit, non-ATPase, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16602]"}, {"versioned_ensembl_gene_id":"ENSG00000182050.13","gene_symbol":"MGAT4C","gene_name":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]","synonyms":"HGNT-IV-H","biotype":"protein_coding","ncbi_id":"25834","summary":null,"start":85955666,"end":86838904,"strand":-1,"description":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]"}, {"versioned_ensembl_gene_id":"ENSG00000218596.2","gene_symbol":"AL162578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156976294,"end":156977072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120805.13","gene_symbol":"ARL1","gene_name":"ADP ribosylation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:692]","synonyms":"ARFL1","biotype":"protein_coding","ncbi_id":"400","summary":"The protein encoded by this gene belongs to the ARL (ADP-ribosylation factor-like) family of proteins, which are structurally related to ADP-ribosylation factors (ARFs). ARFs, described as activators of cholera toxin (CT) ADP-ribosyltransferase activity, regulate intracellular vesicular membrane trafficking, and stimulate a phospholipase D (PLD) isoform. Although, ARL proteins were initially thought not to activate CT or PLD, later work showed that they are weak stimulators of PLD and CT in a phospholipid dependent manner. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":101393120,"end":101407820,"strand":-1,"description":"ADP ribosylation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:692]"}, {"versioned_ensembl_gene_id":"ENSG00000116703.13","gene_symbol":"PDC","gene_name":"phosducin [Source:HGNC Symbol;Acc:HGNC:8759]","synonyms":"MEKA","biotype":"protein_coding","ncbi_id":"5132","summary":"This gene encodes a phosphoprotein, which is located in the outer and inner segments of the rod cells in the retina. This protein may participate in the regulation of visual phototransduction or in the integration of photoreceptor metabolism. It modulates the phototransduction cascade by interacting with the beta and gamma subunits of the retinal G-protein transducin. This gene is a potential candidate gene for retinitis pigmentosa and Usher syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":186443566,"end":186461122,"strand":-1,"description":"phosducin [Source:HGNC Symbol;Acc:HGNC:8759]"}, {"versioned_ensembl_gene_id":"ENSG00000205403.12","gene_symbol":"CFI","gene_name":"complement factor I [Source:HGNC Symbol;Acc:HGNC:5394]","synonyms":"FI,C3b-INA,KAF,IF","biotype":"protein_coding","ncbi_id":"3426","summary":"This gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene. [provided by RefSeq, Dec 2015]","start":109740694,"end":109802179,"strand":-1,"description":"complement factor I [Source:HGNC Symbol;Acc:HGNC:5394]"}, {"versioned_ensembl_gene_id":"ENSG00000183379.8","gene_symbol":"SYNDIG1L","gene_name":"synapse differentiation inducing 1 like [Source:HGNC Symbol;Acc:HGNC:32388]","synonyms":"TMEM90A,IFITMD4,capucin","biotype":"protein_coding","ncbi_id":"646658","summary":null,"start":74405893,"end":74426102,"strand":-1,"description":"synapse differentiation inducing 1 like [Source:HGNC Symbol;Acc:HGNC:32388]"}, {"versioned_ensembl_gene_id":"ENSG00000255382.1","gene_symbol":"AP001646.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82791662,"end":82817146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218520.5","gene_symbol":"AL450346.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63229087,"end":63230110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233217.2","gene_symbol":"MROH3P","gene_name":"maestro heat like repeat family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33122]","synonyms":"C1orf81","biotype":"transcribed_unitary_pseudogene","ncbi_id":"647215","summary":null,"start":200917460,"end":200966668,"strand":1,"description":"maestro heat like repeat family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33122]"}, {"versioned_ensembl_gene_id":"ENSG00000257108.1","gene_symbol":"NHLRC4","gene_name":"NHL repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26700]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283948","summary":null,"start":566996,"end":569495,"strand":1,"description":"NHL repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26700]"}, {"versioned_ensembl_gene_id":"ENSG00000198909.7","gene_symbol":"MAP3K3","gene_name":"mitogen-activated protein kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6855]","synonyms":"MEKK3,MAPKKK3","biotype":"protein_coding","ncbi_id":"4215","summary":"This gene product is a 626-amino acid polypeptide that is 96.5% identical to mouse Mekk3. Its catalytic domain is closely related to those of several other kinases, including mouse Mekk2, tobacco NPK, and yeast Ste11. Northern blot analysis revealed a 4.6-kb transcript that appears to be ubiquitously expressed. This protein directly regulates the stress-activated protein kinase (SAPK) and extracellular signal-regulated protein kinase (ERK) pathways by activating SEK and MEK1/2 respectively; it does not regulate the p38 pathway. In cotransfection assays, it enhanced transcription from a nuclear factor kappa-B (NFKB)-dependent reporter gene, consistent with a role in the SAPK pathway. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":63622415,"end":63696303,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6855]"}, {"versioned_ensembl_gene_id":"ENSG00000162066.14","gene_symbol":"AMDHD2","gene_name":"amidohydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24262]","synonyms":"CGI-14","biotype":"protein_coding","ncbi_id":"51005","summary":null,"start":2520357,"end":2531422,"strand":1,"description":"amidohydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24262]"}, {"versioned_ensembl_gene_id":"ENSG00000229235.1","gene_symbol":"RPL37P18","gene_name":"ribosomal protein L37 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271342","summary":null,"start":34663859,"end":34664101,"strand":-1,"description":"ribosomal protein L37 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35919]"}, {"versioned_ensembl_gene_id":"ENSG00000168495.12","gene_symbol":"POLR3D","gene_name":"RNA polymerase III subunit D [Source:HGNC Symbol;Acc:HGNC:1080]","synonyms":"TSBN51,RPC4,BN51T","biotype":"protein_coding","ncbi_id":"661","summary":"This gene complements a temperature-sensitive mutant isolated from the BHK-21 Syrian hamster cell line. It leads to a block in progression through the G1 phase of the cell cycle at nonpermissive temperatures. [provided by RefSeq, Jul 2008]","start":22245104,"end":22254600,"strand":1,"description":"RNA polymerase III subunit D [Source:HGNC Symbol;Acc:HGNC:1080]"}, {"versioned_ensembl_gene_id":"ENSG00000253894.1","gene_symbol":"AC011124.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63465849,"end":63475482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283005.1","gene_symbol":"CDC27P3","gene_name":"cell division cycle 27 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51754]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723416","summary":null,"start":29746181,"end":29748090,"strand":1,"description":"cell division cycle 27 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51754]"}, {"versioned_ensembl_gene_id":"ENSG00000246366.6","gene_symbol":"LACTB2-AS1","gene_name":"LACTB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27841]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"286190","summary":null,"start":70608577,"end":70663279,"strand":1,"description":"LACTB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27841]"}, {"versioned_ensembl_gene_id":"ENSG00000225487.2","gene_symbol":"AL390119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164921318,"end":164921629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233194.1","gene_symbol":"AL805913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33008496,"end":33008905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168994.13","gene_symbol":"PXDC1","gene_name":"PX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21361]","synonyms":"C6orf145","biotype":"protein_coding","ncbi_id":"221749","summary":null,"start":3722614,"end":3752026,"strand":-1,"description":"PX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21361]"}, {"versioned_ensembl_gene_id":"ENSG00000263635.1","gene_symbol":"AP005242.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15075445,"end":15122767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239305.6","gene_symbol":"RNF103","gene_name":"ring finger protein 103 [Source:HGNC Symbol;Acc:HGNC:12859]","synonyms":"ZFP103,KF1,hkf-1","biotype":"protein_coding","ncbi_id":"7844","summary":"The protein encoded by this gene contains a RING-H2 finger, a motif known to be involved in protein-protein and protein-DNA interactions. This gene is highly expressed in normal cerebellum, but not in the cerebral cortex. The expression of the rat counterpart in the frontal cortex and hippocampus was shown to be induced by elctroconvulsive treatment (ECT) as well as chronic antidepressant treatment, suggesting that this gene may be a molecular target for ECT and antidepressants. The protein is a ubiquitin ligase that functions in the endoplasmic reticulum-associated degradation pathway. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream CHMP3 (charged multivesicular body protein 3) gene. [provided by RefSeq, Oct 2011]","start":86603393,"end":86623866,"strand":-1,"description":"ring finger protein 103 [Source:HGNC Symbol;Acc:HGNC:12859]"}, {"versioned_ensembl_gene_id":"ENSG00000156206.13","gene_symbol":"CFAP161","gene_name":"cilia and flagella associated protein 161 [Source:HGNC Symbol;Acc:HGNC:26782]","synonyms":"FLJ38615,C15orf26","biotype":"protein_coding","ncbi_id":"161502","summary":null,"start":81007033,"end":81149175,"strand":1,"description":"cilia and flagella associated protein 161 [Source:HGNC Symbol;Acc:HGNC:26782]"}, {"versioned_ensembl_gene_id":"ENSG00000268083.5","gene_symbol":"AC008982.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38817471,"end":38840178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279834.1","gene_symbol":"AC068870.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81060953,"end":81063488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259461.1","gene_symbol":"ANP32BP3","gene_name":"acidic nuclear phosphoprotein 32 family member B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44089]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652899","summary":null,"start":81117635,"end":81118340,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44089]"}, {"versioned_ensembl_gene_id":"ENSG00000153561.12","gene_symbol":"RMND5A","gene_name":"required for meiotic nuclear division 5 homolog A [Source:HGNC Symbol;Acc:HGNC:25850]","synonyms":"GID2A,GID2,FLJ13910,RMD5,p44CTLH","biotype":"protein_coding","ncbi_id":"64795","summary":null,"start":86720173,"end":86778041,"strand":1,"description":"required for meiotic nuclear division 5 homolog A [Source:HGNC Symbol;Acc:HGNC:25850]"}, {"versioned_ensembl_gene_id":"ENSG00000184616.8","gene_symbol":"SPDYE12P","gene_name":"speedy/RINGO cell cycle regulator family member E12, pseudogene [Source:HGNC Symbol;Acc:HGNC:51508]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100101268","summary":null,"start":74906673,"end":74913256,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E12, pseudogene [Source:HGNC Symbol;Acc:HGNC:51508]"}, {"versioned_ensembl_gene_id":"ENSG00000069020.18","gene_symbol":"MAST4","gene_name":"microtubule associated serine/threonine kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:19037]","synonyms":"KIAA0303","biotype":"protein_coding","ncbi_id":"375449","summary":"This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":66596361,"end":67169595,"strand":1,"description":"microtubule associated serine/threonine kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:19037]"}, {"versioned_ensembl_gene_id":"ENSG00000279341.1","gene_symbol":"AP000756.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87718667,"end":87721233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229666.1","gene_symbol":"MAST4-AS1","gene_name":"MAST4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40865]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928794","summary":null,"start":67001383,"end":67003953,"strand":-1,"description":"MAST4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40865]"}, {"versioned_ensembl_gene_id":"ENSG00000235273.1","gene_symbol":"CR753509.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29224018,"end":29267104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230015.3","gene_symbol":"AL365184.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":240739419,"end":240739853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224990.1","gene_symbol":"CR753509.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229272,"end":29230202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234872.2","gene_symbol":"AL358176.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240654241,"end":240654625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266614.1","gene_symbol":"AC103808.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76259166,"end":76260114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229441.1","gene_symbol":"CR933537.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215281,"end":29216224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118200.14","gene_symbol":"CAMSAP2","gene_name":"calmodulin regulated spectrin associated protein family member 2 [Source:HGNC Symbol;Acc:HGNC:29188]","synonyms":"KIAA1078,CAMSAP1L1","biotype":"protein_coding","ncbi_id":"23271","summary":null,"start":200739558,"end":200860704,"strand":1,"description":"calmodulin regulated spectrin associated protein family member 2 [Source:HGNC Symbol;Acc:HGNC:29188]"}, {"versioned_ensembl_gene_id":"ENSG00000274930.1","gene_symbol":"AC105227.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50318420,"end":50319024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100523.14","gene_symbol":"DDHD1","gene_name":"DDHD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19714]","synonyms":"SPG28,PA-PLA1,KIAA1705","biotype":"protein_coding","ncbi_id":"80821","summary":"This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":53036745,"end":53153282,"strand":-1,"description":"DDHD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19714]"}, {"versioned_ensembl_gene_id":"ENSG00000228337.1","gene_symbol":"AC096920.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50685551,"end":50685791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236545.1","gene_symbol":"AP001619.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41870633,"end":41872054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179562.2","gene_symbol":"GCC1","gene_name":"GRIP and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19095]","synonyms":"GCC1P,FLJ22035,MGC20706,GCC88","biotype":"protein_coding","ncbi_id":"79571","summary":"The protein encoded by this gene is a peripheral membrane protein. It is sensitive to brefeldin A. This encoded protein contains a GRIP domain which is thought to be used in targeting. It may play a role in the organization of trans-Golgi network subcompartment involved with membrane transport. [provided by RefSeq, Jul 2008]","start":127580618,"end":127593611,"strand":-1,"description":"GRIP and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19095]"}, {"versioned_ensembl_gene_id":"ENSG00000268756.1","gene_symbol":"AC104534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38820166,"end":38823223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188636.3","gene_symbol":"RTL6","gene_name":"retrotransposon Gag like 6 [Source:HGNC Symbol;Acc:HGNC:13343]","synonyms":"SIRH3,Mart6,Mar6,LDOC1L,DKFZp761O17121,dJ1033E15.2","biotype":"protein_coding","ncbi_id":"84247","summary":null,"start":44492572,"end":44498298,"strand":-1,"description":"retrotransposon Gag like 6 [Source:HGNC Symbol;Acc:HGNC:13343]"}, {"versioned_ensembl_gene_id":"ENSG00000141295.13","gene_symbol":"SCRN2","gene_name":"secernin 2 [Source:HGNC Symbol;Acc:HGNC:30381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90507","summary":null,"start":47837692,"end":47841333,"strand":-1,"description":"secernin 2 [Source:HGNC Symbol;Acc:HGNC:30381]"}, {"versioned_ensembl_gene_id":"ENSG00000184588.17","gene_symbol":"PDE4B","gene_name":"phosphodiesterase 4B [Source:HGNC Symbol;Acc:HGNC:8781]","synonyms":"DPDE4","biotype":"protein_coding","ncbi_id":"5142","summary":"This gene is a member of the type IV, cyclic AMP (cAMP)-specific, cyclic nucleotide phosphodiesterase (PDE) family. The encoded protein regulates the cellular concentrations of cyclic nucleotides and thereby play a role in signal transduction. Altered activity of this protein has been associated with schizophrenia and bipolar affective disorder. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":65792514,"end":66374579,"strand":1,"description":"phosphodiesterase 4B [Source:HGNC Symbol;Acc:HGNC:8781]"}, {"versioned_ensembl_gene_id":"ENSG00000235505.7","gene_symbol":"AP002004.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":104901549,"end":104919073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101405.3","gene_symbol":"OXT","gene_name":"oxytocin/neurophysin I prepropeptide [Source:HGNC Symbol;Acc:HGNC:8528]","synonyms":"OXT-NPI,OT-NPI,OT","biotype":"protein_coding","ncbi_id":"5020","summary":"This gene encodes a precursor protein that is processed to produce oxytocin and neurophysin I. Oxytocin is a posterior pituitary hormone which is synthesized as an inactive precursor in the hypothalamus along with its carrier protein neurophysin I. Together with neurophysin, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis, where it is either stored or secreted into the bloodstream. The precursor seems to be activated while it is being transported along the axon to the posterior pituitary. This hormone contracts smooth muscle during parturition and lactation. It is also involved in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. [provided by RefSeq, Dec 2013]","start":3071620,"end":3072517,"strand":1,"description":"oxytocin/neurophysin I prepropeptide [Source:HGNC Symbol;Acc:HGNC:8528]"}, {"versioned_ensembl_gene_id":"ENSG00000140406.3","gene_symbol":"TLNRD1","gene_name":"talin rod domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13519]","synonyms":"MGC99595,MESDC1","biotype":"protein_coding","ncbi_id":"59274","summary":"This gene encodes a protein that is regulated by micro RNA MiR-574-3, and is thought to have an oncogenic function in human bladder cancer. A similar gene in mouse is located in a chromosomal region critical for differentiation of mesoderm, which affects embryo patterning and the formation of heart, muscle, blood, skeleton and the urogenital system. The mouse gene is expressed in early development, and in the adult. [provided by RefSeq, Nov 2016]","start":81000944,"end":81005788,"strand":1,"description":"talin rod domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13519]"}, {"versioned_ensembl_gene_id":"ENSG00000249667.1","gene_symbol":"LINC01259","gene_name":"long intergenic non-protein coding RNA 1259 [Source:HGNC Symbol;Acc:HGNC:49899]","synonyms":"TCONS_00007515","biotype":"lincRNA","ncbi_id":"106144599","summary":null,"start":38509767,"end":38518056,"strand":1,"description":"long intergenic non-protein coding RNA 1259 [Source:HGNC Symbol;Acc:HGNC:49899]"}, {"versioned_ensembl_gene_id":"ENSG00000249534.1","gene_symbol":"LINC01258","gene_name":"long intergenic non-protein coding RNA 1258 [Source:HGNC Symbol;Acc:HGNC:49898]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928776","summary":null,"start":38420662,"end":38523180,"strand":-1,"description":"long intergenic non-protein coding RNA 1258 [Source:HGNC Symbol;Acc:HGNC:49898]"}, {"versioned_ensembl_gene_id":"ENSG00000228818.1","gene_symbol":"AL359918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240142670,"end":240145389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213839.4","gene_symbol":"TMX2P1","gene_name":"thioredoxin related transmembrane protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100233198","summary":null,"start":37885683,"end":37886390,"strand":1,"description":"thioredoxin related transmembrane protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49916]"}, {"versioned_ensembl_gene_id":"ENSG00000279528.1","gene_symbol":"AC115618.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48580741,"end":48581165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183814.15","gene_symbol":"LIN9","gene_name":"lin-9 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:30830]","synonyms":"TGS","biotype":"protein_coding","ncbi_id":"286826","summary":"This gene encodes a tumor suppressor protein that inhibits DNA synthesis and oncogenic transformation through association with the retinoblastoma 1 protein. The encoded protein also interacts with a complex of other cell cycle regulators to repress cell cycle-dependent gene expression in non-dividing cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":226231149,"end":226309869,"strand":-1,"description":"lin-9 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:30830]"}, {"versioned_ensembl_gene_id":"ENSG00000235629.1","gene_symbol":"AC090952.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14648194,"end":14649432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006534.15","gene_symbol":"ALDH3B1","gene_name":"aldehyde dehydrogenase 3 family member B1 [Source:HGNC Symbol;Acc:HGNC:410]","synonyms":"ALDH7","biotype":"protein_coding","ncbi_id":"221","summary":"This gene encodes a member of the aldehyde dehydrogenase protein family. Aldehyde dehydrogenases are a family of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The encoded protein is able to oxidize long-chain fatty aldehydes in vitro, and may play a role in protection from oxidative stress. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":68008578,"end":68029282,"strand":1,"description":"aldehyde dehydrogenase 3 family member B1 [Source:HGNC Symbol;Acc:HGNC:410]"}, {"versioned_ensembl_gene_id":"ENSG00000136891.13","gene_symbol":"TEX10","gene_name":"testis expressed 10 [Source:HGNC Symbol;Acc:HGNC:25988]","synonyms":"Ipi1,FLJ20287,bA208F1.2","biotype":"protein_coding","ncbi_id":"54881","summary":null,"start":100302077,"end":100352939,"strand":-1,"description":"testis expressed 10 [Source:HGNC Symbol;Acc:HGNC:25988]"}, {"versioned_ensembl_gene_id":"ENSG00000271657.1","gene_symbol":"AC018462.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62168862,"end":62171163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232636.2","gene_symbol":"AL360267.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87427200,"end":87447235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255019.1","gene_symbol":"OR5D15P","gene_name":"olfactory receptor family 5 subfamily D member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15282]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81198","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55786964,"end":55787905,"strand":1,"description":"olfactory receptor family 5 subfamily D member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15282]"}, {"versioned_ensembl_gene_id":"ENSG00000180610.10","gene_symbol":"ZBTB12BP","gene_name":"zinc finger and BTB domain containing 12B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37702]","synonyms":"ZNF920,ZBTB12P1,ZBTB12B","biotype":"processed_pseudogene","ncbi_id":"100499252","summary":null,"start":39770081,"end":39771371,"strand":-1,"description":"zinc finger and BTB domain containing 12B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37702]"}, {"versioned_ensembl_gene_id":"ENSG00000227680.1","gene_symbol":"AC108051.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102987323,"end":102988565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232041.1","gene_symbol":"PSMD10P3","gene_name":"proteasome 26S subunit, non-ATPase, 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30152]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338091","summary":null,"start":73036401,"end":73036848,"strand":1,"description":"proteasome 26S subunit, non-ATPase, 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30152]"}, {"versioned_ensembl_gene_id":"ENSG00000107338.9","gene_symbol":"SHB","gene_name":"SH2 domain containing adaptor protein B [Source:HGNC Symbol;Acc:HGNC:10838]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6461","summary":null,"start":37919134,"end":38069211,"strand":-1,"description":"SH2 domain containing adaptor protein B [Source:HGNC Symbol;Acc:HGNC:10838]"}, {"versioned_ensembl_gene_id":"ENSG00000234491.1","gene_symbol":"HNRNPA1P51","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729366","summary":null,"start":206419292,"end":206420238,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]"}, {"versioned_ensembl_gene_id":"ENSG00000117480.15","gene_symbol":"FAAH","gene_name":"fatty acid amide hydrolase [Source:HGNC Symbol;Acc:HGNC:3553]","synonyms":"FAAH-1","biotype":"protein_coding","ncbi_id":"2166","summary":"This gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid amides, including the neuromodulatory compounds anandamide and oleamide. [provided by RefSeq, Jul 2008]","start":46394265,"end":46413848,"strand":1,"description":"fatty acid amide hydrolase [Source:HGNC Symbol;Acc:HGNC:3553]"}, {"versioned_ensembl_gene_id":"ENSG00000219074.1","gene_symbol":"SOD1P1","gene_name":"superoxide dismutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479055","summary":null,"start":53196720,"end":53197159,"strand":-1,"description":"superoxide dismutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45134]"}, {"versioned_ensembl_gene_id":"ENSG00000196104.10","gene_symbol":"SPOCK3","gene_name":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 3 [Source:HGNC Symbol;Acc:HGNC:13565]","synonyms":"testican-3","biotype":"protein_coding","ncbi_id":"50859","summary":"This gene encodes a member of a novel family of calcium-binding proteoglycan proteins that contain thyroglobulin type-1 and Kazal-like domains. The encoded protein and may play a role in adult T-cell leukemia by inhibiting the activity of membrane-type matrix metalloproteinases. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":166733384,"end":167234796,"strand":-1,"description":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 3 [Source:HGNC Symbol;Acc:HGNC:13565]"}, {"versioned_ensembl_gene_id":"ENSG00000277072.4","gene_symbol":"STAG3L2","gene_name":"stromal antigen 3-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33886]","synonyms":"STAG3L2P,MGC131759","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442582","summary":null,"start":74882163,"end":74890610,"strand":-1,"description":"stromal antigen 3-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33886]"}, {"versioned_ensembl_gene_id":"ENSG00000266460.1","gene_symbol":"AC021506.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75844925,"end":75868252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263821.1","gene_symbol":"AP005121.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14978739,"end":14979839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196597.11","gene_symbol":"ZNF782","gene_name":"zinc finger protein 782 [Source:HGNC Symbol;Acc:HGNC:33110]","synonyms":"FLJ16636","biotype":"protein_coding","ncbi_id":"158431","summary":null,"start":96816472,"end":96875623,"strand":-1,"description":"zinc finger protein 782 [Source:HGNC Symbol;Acc:HGNC:33110]"}, {"versioned_ensembl_gene_id":"ENSG00000059758.7","gene_symbol":"CDK17","gene_name":"cyclin dependent kinase 17 [Source:HGNC Symbol;Acc:HGNC:8750]","synonyms":"PCTK2,PCTAIRE2","biotype":"protein_coding","ncbi_id":"5128","summary":"The protein encoded by this gene belongs to the cdc2/cdkx subfamily of the ser/thr family of protein kinases. It has similarity to a rat protein that is thought to play a role in terminally differentiated neurons. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Jul 2010]","start":96278261,"end":96400560,"strand":-1,"description":"cyclin dependent kinase 17 [Source:HGNC Symbol;Acc:HGNC:8750]"}, {"versioned_ensembl_gene_id":"ENSG00000115902.10","gene_symbol":"SLC1A4","gene_name":"solute carrier family 1 member 4 [Source:HGNC Symbol;Acc:HGNC:10942]","synonyms":"SATT,ASCT1","biotype":"protein_coding","ncbi_id":"6509","summary":"The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]","start":64988477,"end":65023865,"strand":1,"description":"solute carrier family 1 member 4 [Source:HGNC Symbol;Acc:HGNC:10942]"}, {"versioned_ensembl_gene_id":"ENSG00000257169.1","gene_symbol":"AC125612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96386818,"end":96387194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261745.2","gene_symbol":"AL512347.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":53125644,"end":53126146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273521.1","gene_symbol":"AL162274.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131980240,"end":131981337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116918.13","gene_symbol":"TSNAX","gene_name":"translin associated factor X [Source:HGNC Symbol;Acc:HGNC:12380]","synonyms":"TRAX","biotype":"protein_coding","ncbi_id":"7257","summary":"This gene encodes a protein which specifically interacts with translin, a DNA-binding protein that binds consensus sequences at breakpoint junctions of chromosomal translocations. The encoded protein contains bipartite nuclear targeting sequences that may provide nuclear transport for translin, which lacks any nuclear targeting motifs. [provided by RefSeq, Jul 2008]","start":231528653,"end":231566524,"strand":1,"description":"translin associated factor X [Source:HGNC Symbol;Acc:HGNC:12380]"}, {"versioned_ensembl_gene_id":"ENSG00000077514.8","gene_symbol":"POLD3","gene_name":"DNA polymerase delta 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:20932]","synonyms":"P66,KIAA0039,PPP1R128,P68","biotype":"protein_coding","ncbi_id":"10714","summary":"This gene encodes the 66-kDa subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. The encoded protein plays a role in regulating the activity of DNA polymerase delta through interactions with other subunits and the processivity cofactor proliferating cell nuclear antigen (PCNA). Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]","start":74493851,"end":74669117,"strand":1,"description":"DNA polymerase delta 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:20932]"}, {"versioned_ensembl_gene_id":"ENSG00000254201.1","gene_symbol":"AC068880.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19246350,"end":19249240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236026.1","gene_symbol":"AC009237.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95606924,"end":95607152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271003.1","gene_symbol":"AC009237.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95607073,"end":95616592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254762.1","gene_symbol":"AP001107.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66267635,"end":66268129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103888.16","gene_symbol":"CEMIP","gene_name":"cell migration inducing hyaluronan binding protein [Source:HGNC Symbol;Acc:HGNC:29213]","synonyms":"TMEM2L,KIAA1199,IR2155535,HYBID","biotype":"protein_coding","ncbi_id":"57214","summary":null,"start":80779343,"end":80951776,"strand":1,"description":"cell migration inducing hyaluronan binding protein [Source:HGNC Symbol;Acc:HGNC:29213]"}, {"versioned_ensembl_gene_id":"ENSG00000250337.5","gene_symbol":"LINC01021","gene_name":"long intergenic non-protein coding RNA 1021 [Source:HGNC Symbol;Acc:HGNC:48995]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643401","summary":null,"start":27472292,"end":27496401,"strand":1,"description":"long intergenic non-protein coding RNA 1021 [Source:HGNC Symbol;Acc:HGNC:48995]"}, {"versioned_ensembl_gene_id":"ENSG00000226803.7","gene_symbol":"AL136311.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57114894,"end":57174236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206292.13","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-DNA,HLA-D0-alpha,HLA-DZA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":32932859,"end":32938293,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000134258.16","gene_symbol":"VTCN1","gene_name":"V-set domain containing T-cell activation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28873]","synonyms":"FLJ22418,B7X,B7S1,B7H4,B7-H4","biotype":"protein_coding","ncbi_id":"79679","summary":"This gene encodes a protein belonging to the B7 costimulatory protein family. Proteins in this family are present on the surface of antigen-presenting cells and interact with ligand bound to receptors on the surface of T cells. Studies have shown that high levels of the encoded protein has been correlated with tumor progression. A pseudogene of this gene is located on chromosome 20. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":117143587,"end":117210960,"strand":-1,"description":"V-set domain containing T-cell activation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28873]"}, {"versioned_ensembl_gene_id":"ENSG00000230847.4","gene_symbol":"AC044797.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71074225,"end":71093193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269681.1","gene_symbol":"AC063977.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51155288,"end":51155624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260121.1","gene_symbol":"AC138028.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88718615,"end":88720459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248228.1","gene_symbol":"SLIT2-IT1","gene_name":"SLIT2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41383]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100505893","summary":null,"start":20392189,"end":20394856,"strand":1,"description":"SLIT2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41383]"}, {"versioned_ensembl_gene_id":"ENSG00000176769.9","gene_symbol":"TCERG1L","gene_name":"transcription elongation regulator 1 like [Source:HGNC Symbol;Acc:HGNC:23533]","synonyms":"FLJ38950","biotype":"protein_coding","ncbi_id":"256536","summary":null,"start":131092391,"end":131311721,"strand":-1,"description":"transcription elongation regulator 1 like [Source:HGNC Symbol;Acc:HGNC:23533]"}, {"versioned_ensembl_gene_id":"ENSG00000273791.1","gene_symbol":"AC007204.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19908268,"end":19909146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164621.5","gene_symbol":"SMAD5-AS1","gene_name":"SMAD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30586]","synonyms":"DAMS,SMAD5OS","biotype":"antisense_RNA","ncbi_id":"9597","summary":null,"start":136129507,"end":136134890,"strand":-1,"description":"SMAD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30586]"}, {"versioned_ensembl_gene_id":"ENSG00000240770.5","gene_symbol":"C21orf91-OT1","gene_name":"C21orf91 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:16729]","synonyms":"NCRNA00285,D21S2089E","biotype":"lincRNA","ncbi_id":"246312","summary":null,"start":17763315,"end":17792523,"strand":-1,"description":"C21orf91 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:16729]"}, {"versioned_ensembl_gene_id":"ENSG00000112182.14","gene_symbol":"BACH2","gene_name":"BTB domain and CNC homolog 2 [Source:HGNC Symbol;Acc:HGNC:14078]","synonyms":"BTBD25","biotype":"protein_coding","ncbi_id":"60468","summary":null,"start":89926529,"end":90296908,"strand":-1,"description":"BTB domain and CNC homolog 2 [Source:HGNC Symbol;Acc:HGNC:14078]"}, {"versioned_ensembl_gene_id":"ENSG00000255107.1","gene_symbol":"AC079089.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69859264,"end":69860540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144837.8","gene_symbol":"PLA1A","gene_name":"phospholipase A1 member A [Source:HGNC Symbol;Acc:HGNC:17661]","synonyms":"ps-PLA1","biotype":"protein_coding","ncbi_id":"51365","summary":"The protein encoded by this gene is a phospholipase that hydrolyzes fatty acids at the sn-1 position of phosphatidylserine and 1-acyl-2-lysophosphatidylserine. This secreted protein hydrolyzes phosphatidylserine in liposomes. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":119597842,"end":119629811,"strand":1,"description":"phospholipase A1 member A [Source:HGNC Symbol;Acc:HGNC:17661]"}, {"versioned_ensembl_gene_id":"ENSG00000272164.1","gene_symbol":"AC005972.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63004672,"end":63005152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065882.15","gene_symbol":"TBC1D1","gene_name":"TBC1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:11578]","synonyms":"TBC1,TBC,KIAA1108","biotype":"protein_coding","ncbi_id":"23216","summary":"TBC1D1 is the founding member of a family of proteins sharing a 180- to 200-amino acid TBC domain presumed to have a role in regulating cell growth and differentiation. These proteins share significant homology with TRE2 (USP6; MIM 604334), yeast Bub2, and CDC16 (MIM 603461) (White et al., 2000 [PubMed 10965142]).[supplied by OMIM, Mar 2008]","start":37891087,"end":38139175,"strand":1,"description":"TBC1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:11578]"}, {"versioned_ensembl_gene_id":"ENSG00000265262.1","gene_symbol":"TRMT112P3","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44022]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729667","summary":null,"start":62950831,"end":62951188,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44022]"}, {"versioned_ensembl_gene_id":"ENSG00000120158.11","gene_symbol":"RCL1","gene_name":"RNA terminal phosphate cyclase like 1 [Source:HGNC Symbol;Acc:HGNC:17687]","synonyms":"RPCL1,RNAC","biotype":"protein_coding","ncbi_id":"10171","summary":null,"start":4792869,"end":4885917,"strand":1,"description":"RNA terminal phosphate cyclase like 1 [Source:HGNC Symbol;Acc:HGNC:17687]"}, {"versioned_ensembl_gene_id":"ENSG00000228289.1","gene_symbol":"AL355862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163769339,"end":163769691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219240.2","gene_symbol":"AL353692.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89886156,"end":89887848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265702.1","gene_symbol":"AC005821.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62699244,"end":62737922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146374.13","gene_symbol":"RSPO3","gene_name":"R-spondin 3 [Source:HGNC Symbol;Acc:HGNC:20866]","synonyms":"THSD2,FLJ14440","biotype":"protein_coding","ncbi_id":"84870","summary":"This gene belongs to the R-spondin family. The encoded protein plays a role in the regulation of Wnt (wingless-type MMTV integration site family)/beta-catenin and Wnt/planar cell polarity (PCP) signaling pathways, which are involved in development, cell growth and disease pathogenesis. Genome-wide association studies suggest a correlation of this gene with bone mineral density and risk of fracture. This gene may be involved in tumor development. [provided by RefSeq, Jul 2013]","start":127118604,"end":127197765,"strand":1,"description":"R-spondin 3 [Source:HGNC Symbol;Acc:HGNC:20866]"}, {"versioned_ensembl_gene_id":"ENSG00000145147.19","gene_symbol":"SLIT2","gene_name":"slit guidance ligand 2 [Source:HGNC Symbol;Acc:HGNC:11086]","synonyms":"Slit-2,SLIL3","biotype":"protein_coding","ncbi_id":"9353","summary":"This gene encodes a member of the slit family of secreted glycoproteins, which are ligands for the Robo family of immunoglobulin receptors. Slit proteins play highly conserved roles in axon guidance and neuronal migration and may also have functions during other cell migration processes including leukocyte migration. Members of the slit family are characterized by an N-terminal signal peptide, four leucine-rich repeats, nine epidermal growth factor repeats, and a C-terminal cysteine knot. Proteolytic processing of this protein gives rise to an N-terminal fragment that contains the four leucine-rich repeats and five epidermal growth factor repeats and a C-terminal fragment that contains four epidermal growth factor repeats and the cysteine knot. Both full length and cleaved proteins are secreted extracellularly and can function in axon repulsion as well as other specific processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":20253260,"end":20620561,"strand":1,"description":"slit guidance ligand 2 [Source:HGNC Symbol;Acc:HGNC:11086]"}, {"versioned_ensembl_gene_id":"ENSG00000248475.5","gene_symbol":"AC016642.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58741581,"end":58817099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148483.8","gene_symbol":"TMEM236","gene_name":"transmembrane protein 236 [Source:HGNC Symbol;Acc:HGNC:23473]","synonyms":"FAM23B,FAM23A,bA16O1.2,bA162I21.2","biotype":"protein_coding","ncbi_id":"653567","summary":null,"start":17752252,"end":17800868,"strand":1,"description":"transmembrane protein 236 [Source:HGNC Symbol;Acc:HGNC:23473]"}, {"versioned_ensembl_gene_id":"ENSG00000255147.1","gene_symbol":"AP003385.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67749043,"end":67756968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279567.1","gene_symbol":"AC005703.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15365323,"end":15365877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253997.1","gene_symbol":"AC090142.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104990308,"end":104990692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233043.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33298642,"end":33301626,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000116690.12","gene_symbol":"PRG4","gene_name":"proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:9364]","synonyms":"SZP,MSF,JCAP,HAPO,CACP,FLJ32635,bG174L6.2","biotype":"protein_coding","ncbi_id":"10216","summary":"The protein encoded by this gene is a large proteoglycan that is synthesized by chondrocytes located at the surface of articular cartilage and by some synovial lining cells. This protein contains both chondroitin sulfate and keratan sulfate glycosaminoglycans. It functions as a boundary lubricant at the cartilage surface and contributes to the elastic absorption and energy dissipation of synovial fluid. Mutations in this gene result in camptodactyly-arthropathy-coxa vara-pericarditis syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":186296279,"end":186314562,"strand":1,"description":"proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:9364]"}, {"versioned_ensembl_gene_id":"ENSG00000243171.1","gene_symbol":"AC041039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105287830,"end":105288365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167759.12","gene_symbol":"KLK13","gene_name":"kallikrein related peptidase 13 [Source:HGNC Symbol;Acc:HGNC:6361]","synonyms":"KLK-L4","biotype":"protein_coding","ncbi_id":"26085","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Expression of this gene is regulated by steroid hormones and may be useful as a marker for breast cancer. [provided by RefSeq, Jan 2017]","start":51056206,"end":51065114,"strand":-1,"description":"kallikrein related peptidase 13 [Source:HGNC Symbol;Acc:HGNC:6361]"}, {"versioned_ensembl_gene_id":"ENSG00000281008.1","gene_symbol":"AC004808.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78134079,"end":78134851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249863.2","gene_symbol":"AC021106.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37868292,"end":37869978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277351.1","gene_symbol":"AC013553.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65049188,"end":65049802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278763.1","gene_symbol":"FAM27B","gene_name":"family with sequence similarity 27 member B [Source:HGNC Symbol;Acc:HGNC:23667]","synonyms":"FAM27A2,bA12A20.3","biotype":"processed_pseudogene","ncbi_id":"100133121","summary":null,"start":67725690,"end":67725902,"strand":-1,"description":"family with sequence similarity 27 member B [Source:HGNC Symbol;Acc:HGNC:23667]"}, {"versioned_ensembl_gene_id":"ENSG00000225177.5","gene_symbol":"AL590617.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138692548,"end":138697288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115685.14","gene_symbol":"PPP1R7","gene_name":"protein phosphatase 1 regulatory subunit 7 [Source:HGNC Symbol;Acc:HGNC:9295]","synonyms":"sds22","biotype":"protein_coding","ncbi_id":"5510","summary":"This gene encodes a protein subunit that regulates the activity of the serine/threonine phosphatase, protein phosphatase-1. The encoded protein is required for completion of the mitotic cycle and for targeting protein phosphatase-1 to mitotic kinetochores. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":241149576,"end":241183652,"strand":1,"description":"protein phosphatase 1 regulatory subunit 7 [Source:HGNC Symbol;Acc:HGNC:9295]"}, {"versioned_ensembl_gene_id":"ENSG00000088543.14","gene_symbol":"C3orf18","gene_name":"chromosome 3 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:24837]","synonyms":"G20","biotype":"protein_coding","ncbi_id":"51161","summary":null,"start":50558025,"end":50571027,"strand":-1,"description":"chromosome 3 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:24837]"}, {"versioned_ensembl_gene_id":"ENSG00000243709.1","gene_symbol":"LEFTY1","gene_name":"left-right determination factor 1 [Source:HGNC Symbol;Acc:HGNC:6552]","synonyms":"LEFTYB,LEFTB","biotype":"protein_coding","ncbi_id":"10637","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which plays a role in left-right asymmetry determination of organ systems during development. This gene is closely linked to both a related family member and a related pseudogene. [provided by RefSeq, Aug 2016]","start":225886282,"end":225911382,"strand":-1,"description":"left-right determination factor 1 [Source:HGNC Symbol;Acc:HGNC:6552]"}, {"versioned_ensembl_gene_id":"ENSG00000185246.17","gene_symbol":"PRPF39","gene_name":"pre-mRNA processing factor 39 [Source:HGNC Symbol;Acc:HGNC:20314]","synonyms":"FLJ20666,FLJ11128","biotype":"protein_coding","ncbi_id":"55015","summary":null,"start":45084099,"end":45116282,"strand":1,"description":"pre-mRNA processing factor 39 [Source:HGNC Symbol;Acc:HGNC:20314]"}, {"versioned_ensembl_gene_id":"ENSG00000250536.1","gene_symbol":"ABHD17AP3","gene_name":"abhydrolase domain containing 17A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34041]","synonyms":"FAM108A4P,FAM108A4","biotype":"unprocessed_pseudogene","ncbi_id":"648359","summary":null,"start":214605470,"end":214608840,"strand":-1,"description":"abhydrolase domain containing 17A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34041]"}, {"versioned_ensembl_gene_id":"ENSG00000236065.2","gene_symbol":"AL020995.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32987075,"end":33032469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130958.11","gene_symbol":"SLC35D2","gene_name":"solute carrier family 35 member D2 [Source:HGNC Symbol;Acc:HGNC:20799]","synonyms":"UGTrel8,SQV7L","biotype":"protein_coding","ncbi_id":"11046","summary":"Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]","start":96320706,"end":96383710,"strand":-1,"description":"solute carrier family 35 member D2 [Source:HGNC Symbol;Acc:HGNC:20799]"}, {"versioned_ensembl_gene_id":"ENSG00000127022.14","gene_symbol":"CANX","gene_name":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]","synonyms":"P90,IP90,CNX","biotype":"protein_coding","ncbi_id":"821","summary":"This gene encodes a member of the calnexin family of molecular chaperones. The encoded protein is a calcium-binding, endoplasmic reticulum (ER)-associated protein that interacts transiently with newly synthesized N-linked glycoproteins, facilitating protein folding and assembly. It may also play a central role in the quality control of protein folding by retaining incorrectly folded protein subunits within the ER for degradation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2018]","start":179678628,"end":179730925,"strand":1,"description":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]"}, {"versioned_ensembl_gene_id":"ENSG00000140943.16","gene_symbol":"MBTPS1","gene_name":"membrane bound transcription factor peptidase, site 1 [Source:HGNC Symbol;Acc:HGNC:15456]","synonyms":"SKI-1,S1P,PCSK8,KIAA0091","biotype":"protein_coding","ncbi_id":"8720","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the cis/medial-Golgi where a second autocatalytic event takes place and the catalytic activity is acquired. It encodes a type 1 membrane bound protease which is ubiquitously expressed and regulates cholesterol or lipid homeostasis via cleavage of substrates at non-basic residues. Mutations in this gene may be associated with lysosomal dysfunction. [provided by RefSeq, Feb 2014]","start":84053761,"end":84116906,"strand":-1,"description":"membrane bound transcription factor peptidase, site 1 [Source:HGNC Symbol;Acc:HGNC:15456]"}, {"versioned_ensembl_gene_id":"ENSG00000206379.12","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30717966,"end":30732991,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000267693.1","gene_symbol":"AC011477.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19768731,"end":19768989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226025.9","gene_symbol":"LGALS17A","gene_name":"galectin 14 pseudogene [Source:NCBI gene;Acc:400696]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400696","summary":null,"start":39679374,"end":39686373,"strand":1,"description":"galectin 14 pseudogene [Source:NCBI gene;Acc:400696]"}, {"versioned_ensembl_gene_id":"ENSG00000112200.16","gene_symbol":"ZNF451","gene_name":"zinc finger protein 451 [Source:HGNC Symbol;Acc:HGNC:21091]","synonyms":"KIAA1702,KIAA0576,dJ417I1.1,COASTER","biotype":"protein_coding","ncbi_id":"26036","summary":null,"start":57086844,"end":57170307,"strand":1,"description":"zinc finger protein 451 [Source:HGNC Symbol;Acc:HGNC:21091]"}, {"versioned_ensembl_gene_id":"ENSG00000183765.20","gene_symbol":"CHEK2","gene_name":"checkpoint kinase 2 [Source:HGNC Symbol;Acc:HGNC:16627]","synonyms":"RAD53,PP1425,HuCds1,CHK2,CDS1,bA444G7","biotype":"protein_coding","ncbi_id":"11200","summary":"In response to DNA damage and replication blocks, cell cycle progression is halted through the control of critical cell cycle regulators. The protein encoded by this gene is a cell cycle checkpoint regulator and putative tumor suppressor. It contains a forkhead-associated protein interaction domain essential for activation in response to DNA damage and is rapidly phosphorylated in response to replication blocks and DNA damage. When activated, the encoded protein is known to inhibit CDC25C phosphatase, preventing entry into mitosis, and has been shown to stabilize the tumor suppressor protein p53, leading to cell cycle arrest in G1. In addition, this protein interacts with and phosphorylates BRCA1, allowing BRCA1 to restore survival after DNA damage. Mutations in this gene have been linked with Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53. Also, mutations in this gene are thought to confer a predisposition to sarcomas, breast cancer, and brain tumors. This nuclear protein is a member of the CDS1 subfamily of serine/threonine protein kinases. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":28687743,"end":28742422,"strand":-1,"description":"checkpoint kinase 2 [Source:HGNC Symbol;Acc:HGNC:16627]"}, {"versioned_ensembl_gene_id":"ENSG00000134744.13","gene_symbol":"ZCCHC11","gene_name":"zinc finger CCHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:28981]","synonyms":"KIAA0191,TUT4,PAPD3","biotype":"protein_coding","ncbi_id":"23318","summary":"ZCCHC11 is an RNA uridyltransferase (EC 2.7.7.52) that uses UTP to add uridines to the 3-prime end of substrate RNA molecules (Jones et al., 2009 [PubMed 19701194]).[supplied by OMIM, Jan 2011]","start":52408282,"end":52553487,"strand":-1,"description":"zinc finger CCHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:28981]"}, {"versioned_ensembl_gene_id":"ENSG00000115042.9","gene_symbol":"FAHD2A","gene_name":"fumarylacetoacetate hydrolase domain containing 2A [Source:HGNC Symbol;Acc:HGNC:24252]","synonyms":"CGI-105","biotype":"protein_coding","ncbi_id":"51011","summary":null,"start":95402721,"end":95416616,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 2A [Source:HGNC Symbol;Acc:HGNC:24252]"}, {"versioned_ensembl_gene_id":"ENSG00000273063.1","gene_symbol":"AC007250.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58241349,"end":58241686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273851.1","gene_symbol":"AC027088.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":69022230,"end":69024176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227432.1","gene_symbol":"AC053503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219482073,"end":219516877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133030.20","gene_symbol":"MPRIP","gene_name":"myosin phosphatase Rho interacting protein [Source:HGNC Symbol;Acc:HGNC:30321]","synonyms":"RHOIP3,p116Rip,M-RIP","biotype":"protein_coding","ncbi_id":"23164","summary":null,"start":17042545,"end":17217679,"strand":1,"description":"myosin phosphatase Rho interacting protein [Source:HGNC Symbol;Acc:HGNC:30321]"}, {"versioned_ensembl_gene_id":"ENSG00000251323.2","gene_symbol":"AP003086.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78423982,"end":78429836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119705.9","gene_symbol":"SLIRP","gene_name":"SRA stem-loop interacting RNA binding protein [Source:HGNC Symbol;Acc:HGNC:20495]","synonyms":"C14orf156,DC50","biotype":"protein_coding","ncbi_id":"81892","summary":"Steroid receptor RNA activator (SRA, or SRA1; MIM 603819) is a complex RNA molecule containing multiple stable stem-loop structures that functions in coactivation of nuclear receptors. SLIRP interacts with stem-loop structure-7 of SRA (STR7) and modulates nuclear receptor transactivation (Hatchell et al., 2006 [PubMed 16762838]).[supplied by OMIM, Mar 2008]","start":77708071,"end":77761104,"strand":1,"description":"SRA stem-loop interacting RNA binding protein [Source:HGNC Symbol;Acc:HGNC:20495]"}, {"versioned_ensembl_gene_id":"ENSG00000232259.1","gene_symbol":"AL158166.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127929376,"end":127934517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189233.11","gene_symbol":"NUGGC","gene_name":"nuclear GTPase, germinal center associated [Source:HGNC Symbol;Acc:HGNC:33550]","synonyms":"SLIP-GC,HMFN0672,C8orf80","biotype":"protein_coding","ncbi_id":"389643","summary":null,"start":28021964,"end":28083871,"strand":-1,"description":"nuclear GTPase, germinal center associated [Source:HGNC Symbol;Acc:HGNC:33550]"}, {"versioned_ensembl_gene_id":"ENSG00000278563.2","gene_symbol":"MGAM2","gene_name":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93432","summary":null,"start":142111749,"end":142222324,"strand":1,"description":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]"}, {"versioned_ensembl_gene_id":"ENSG00000131944.9","gene_symbol":"FAAP24","gene_name":"Fanconi anemia core complex associated protein 24 [Source:HGNC Symbol;Acc:HGNC:28467]","synonyms":"C19orf40,MGC32020,FLJ46828","biotype":"protein_coding","ncbi_id":"91442","summary":"FAAP24 is a component of the Fanconi anemia (FA) core complex (see MIM 227650), which plays a crucial role in DNA damage response (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008]","start":32972209,"end":32978222,"strand":1,"description":"Fanconi anemia core complex associated protein 24 [Source:HGNC Symbol;Acc:HGNC:28467]"}, {"versioned_ensembl_gene_id":"ENSG00000278133.1","gene_symbol":"AC135050.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31122235,"end":31124064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227650.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31598491,"end":31598764,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000275610.1","gene_symbol":"DUX4L21","gene_name":"double homeobox 4 like 21 [Source:HGNC Symbol;Acc:HGNC:50802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723518","summary":null,"start":133680369,"end":133681637,"strand":1,"description":"double homeobox 4 like 21 [Source:HGNC Symbol;Acc:HGNC:50802]"}, {"versioned_ensembl_gene_id":"ENSG00000213079.9","gene_symbol":"SCAF8","gene_name":"SR-related CTD associated factor 8 [Source:HGNC Symbol;Acc:HGNC:20959]","synonyms":"RBM16,KIAA1116","biotype":"protein_coding","ncbi_id":"22828","summary":null,"start":154733325,"end":154834244,"strand":1,"description":"SR-related CTD associated factor 8 [Source:HGNC Symbol;Acc:HGNC:20959]"}, {"versioned_ensembl_gene_id":"ENSG00000253744.1","gene_symbol":"AC025442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66144156,"end":66144795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248802.1","gene_symbol":"AC078850.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128582999,"end":128601407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166260.11","gene_symbol":"COX11","gene_name":"COX11, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2261]","synonyms":"COX11P","biotype":"protein_coding","ncbi_id":"1353","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be a heme A biosynthetic enzyme involved in COX formation, according to the yeast mutant studies. However, the studies in Rhodobacter sphaeroides suggest that this gene is not required for heme A biosynthesis, but required for stable formation of the Cu(B) and magnesium centers of COX. This human protein is predicted to contain a transmembrane domain localized in the mitochondrial inner membrane. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene has been found on chromosome 6. [provided by RefSeq, Jun 2009]","start":54951902,"end":54968785,"strand":-1,"description":"COX11, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2261]"}, {"versioned_ensembl_gene_id":"ENSG00000267277.1","gene_symbol":"AC024575.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11368123,"end":11374935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273055.1","gene_symbol":"AC005046.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107942116,"end":107942740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172867.3","gene_symbol":"KRT2","gene_name":"keratin 2 [Source:HGNC Symbol;Acc:HGNC:6439]","synonyms":"KRTE,KRT2A","biotype":"protein_coding","ncbi_id":"3849","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in this gene have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52644558,"end":52652164,"strand":-1,"description":"keratin 2 [Source:HGNC Symbol;Acc:HGNC:6439]"}, {"versioned_ensembl_gene_id":"ENSG00000127445.13","gene_symbol":"PIN1","gene_name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 [Source:HGNC Symbol;Acc:HGNC:8988]","synonyms":"dod","biotype":"protein_coding","ncbi_id":"5300","summary":"Peptidyl-prolyl cis/trans isomerases (PPIases) catalyze the cis/trans isomerization of peptidyl-prolyl peptide bonds. This gene encodes one of the PPIases, which specifically binds to phosphorylated ser/thr-pro motifs to catalytically regulate the post-phosphorylation conformation of its substrates. The conformational regulation catalyzed by this PPIase has a profound impact on key proteins involved in the regulation of cell growth, genotoxic and other stress responses, the immune response, induction and maintenance of pluripotency, germ cell development, neuronal differentiation, and survival. This enzyme also plays a key role in the pathogenesis of Alzheimer's disease and many cancers. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011]","start":9835257,"end":9849682,"strand":1,"description":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 [Source:HGNC Symbol;Acc:HGNC:8988]"}, {"versioned_ensembl_gene_id":"ENSG00000245928.2","gene_symbol":"AC112719.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75980790,"end":76005942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236889.1","gene_symbol":"AC244035.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206175060,"end":206177246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248929.1","gene_symbol":"HIGD1AP3","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42998]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100859920","summary":null,"start":174632932,"end":174633209,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42998]"}, {"versioned_ensembl_gene_id":"ENSG00000138744.14","gene_symbol":"NAAA","gene_name":"N-acylethanolamine acid amidase [Source:HGNC Symbol;Acc:HGNC:736]","synonyms":"ASAHL","biotype":"protein_coding","ncbi_id":"27163","summary":"This gene encodes an N-acylethanolamine-hydrolyzing enzyme which is highly similar to acid ceramidase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75913657,"end":75941051,"strand":-1,"description":"N-acylethanolamine acid amidase [Source:HGNC Symbol;Acc:HGNC:736]"}, {"versioned_ensembl_gene_id":"ENSG00000253474.1","gene_symbol":"AC022568.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49168539,"end":49228925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279649.1","gene_symbol":"AC020978.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68290087,"end":68292790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109944.10","gene_symbol":"C11orf63","gene_name":"chromosome 11 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:26288]","synonyms":"Jhy,FLJ23554","biotype":"protein_coding","ncbi_id":"79864","summary":null,"start":122882528,"end":122959798,"strand":1,"description":"chromosome 11 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:26288]"}, {"versioned_ensembl_gene_id":"ENSG00000137692.11","gene_symbol":"DCUN1D5","gene_name":"defective in cullin neddylation 1 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28409]","synonyms":"MGC2714,FLJ32431","biotype":"protein_coding","ncbi_id":"84259","summary":null,"start":103062076,"end":103092215,"strand":-1,"description":"defective in cullin neddylation 1 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28409]"}, {"versioned_ensembl_gene_id":"ENSG00000275173.1","gene_symbol":"AC243571.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37798894,"end":37802788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105355.8","gene_symbol":"PLIN3","gene_name":"perilipin 3 [Source:HGNC Symbol;Acc:HGNC:16893]","synonyms":"TIP47,PP17,M6PRBP1","biotype":"protein_coding","ncbi_id":"10226","summary":"Mannose 6-phophate receptors (MPRs) deliver lysosomal hydrolase from the Golgi to endosomes and then return to the Golgi complex. The protein encoded by this gene interacts with the cytoplasmic domains of both cation-independent and cation-dependent MPRs, and is required for endosome-to-Golgi transport. This protein also binds directly to the GTPase RAB9 (RAB9A), a member of the RAS oncogene family. The interaction with RAB9 has been shown to increase the affinity of this protein for its cargo. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2009]","start":4838341,"end":4867768,"strand":-1,"description":"perilipin 3 [Source:HGNC Symbol;Acc:HGNC:16893]"}, {"versioned_ensembl_gene_id":"ENSG00000267484.1","gene_symbol":"AC027319.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4838332,"end":4838907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171574.17","gene_symbol":"ZNF584","gene_name":"zinc finger protein 584 [Source:HGNC Symbol;Acc:HGNC:27318]","synonyms":"FLJ39899","biotype":"protein_coding","ncbi_id":"201514","summary":null,"start":58401504,"end":58418327,"strand":1,"description":"zinc finger protein 584 [Source:HGNC Symbol;Acc:HGNC:27318]"}, {"versioned_ensembl_gene_id":"ENSG00000261683.1","gene_symbol":"LINC00838","gene_name":"long intergenic non-protein coding RNA 838 [Source:HGNC Symbol;Acc:HGNC:44963]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505583","summary":null,"start":33759713,"end":33772658,"strand":-1,"description":"long intergenic non-protein coding RNA 838 [Source:HGNC Symbol;Acc:HGNC:44963]"}, {"versioned_ensembl_gene_id":"ENSG00000254505.9","gene_symbol":"CHMP4A","gene_name":"charged multivesicular body protein 4A [Source:HGNC Symbol;Acc:HGNC:20274]","synonyms":"HSPC134,C14orf123,VPS32A","biotype":"protein_coding","ncbi_id":"29082","summary":"CHMP4A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":24209583,"end":24213869,"strand":-1,"description":"charged multivesicular body protein 4A [Source:HGNC Symbol;Acc:HGNC:20274]"}, {"versioned_ensembl_gene_id":"ENSG00000154639.18","gene_symbol":"CXADR","gene_name":"CXADR, Ig-like cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:2559]","synonyms":"CAR","biotype":"protein_coding","ncbi_id":"1525","summary":"The protein encoded by this gene is a type I membrane receptor for group B coxsackieviruses and subgroup C adenoviruses. Several transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene are found on chromosomes 15, 18, and 21. [provided by RefSeq, May 2011]","start":17512382,"end":17593579,"strand":1,"description":"CXADR, Ig-like cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:2559]"}, {"versioned_ensembl_gene_id":"ENSG00000221990.4","gene_symbol":"EXOC3-AS1","gene_name":"EXOC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25175]","synonyms":"C5orf55","biotype":"antisense_RNA","ncbi_id":"116349","summary":null,"start":441498,"end":443160,"strand":-1,"description":"EXOC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25175]"}, {"versioned_ensembl_gene_id":"ENSG00000104970.10","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"LENG12,FLJ00060","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54532692,"end":54545771,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000134183.11","gene_symbol":"GNAT2","gene_name":"G protein subunit alpha transducin 2 [Source:HGNC Symbol;Acc:HGNC:4394]","synonyms":"ACHM4","biotype":"protein_coding","ncbi_id":"2780","summary":"Transducin is a 3-subunit guanine nucleotide-binding protein (G protein) which stimulates the coupling of rhodopsin and cGMP-phoshodiesterase during visual impulses. The transducin alpha subunits in rods and cones are encoded by separate genes. This gene encodes the alpha subunit in cones. [provided by RefSeq, Jul 2008]","start":109603267,"end":109619929,"strand":-1,"description":"G protein subunit alpha transducin 2 [Source:HGNC Symbol;Acc:HGNC:4394]"}, {"versioned_ensembl_gene_id":"ENSG00000188242.4","gene_symbol":"PP7080","gene_name":"uncharacterized LOC25845 [Source:NCBI gene;Acc:25845]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"25845","summary":null,"start":466124,"end":473098,"strand":-1,"description":"uncharacterized LOC25845 [Source:NCBI gene;Acc:25845]"}, {"versioned_ensembl_gene_id":"ENSG00000168014.16","gene_symbol":"C2CD3","gene_name":"C2 calcium dependent domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24564]","synonyms":"DKFZP586P0123","biotype":"protein_coding","ncbi_id":"26005","summary":"This gene encodes a protein that functions as a regulator of centriole elongation. Studies of the orthologous mouse protein show that it promotes centriolar distal appendage assembly and is also required for the recruitment of other ciliogenic proteins, including intraflagellar transport proteins. Mutations in this gene cause orofaciodigital syndrome XIV (OFD14), a ciliopathy resulting in malformations of the oral cavity, face and digits. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":74012714,"end":74171210,"strand":-1,"description":"C2 calcium dependent domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24564]"}, {"versioned_ensembl_gene_id":"ENSG00000244251.1","gene_symbol":"AC013356.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40480752,"end":40481315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224762.1","gene_symbol":"CR769776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64473040,"end":64473826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267248.1","gene_symbol":"AC025048.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":60126535,"end":60135644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178732.5","gene_symbol":"GP5","gene_name":"glycoprotein V platelet [Source:HGNC Symbol;Acc:HGNC:4443]","synonyms":"CD42d","biotype":"protein_coding","ncbi_id":"2814","summary":"Human platelet glycoprotein V (GP5) is a part of the Ib-V-IX system of surface glycoproteins that constitute the receptor for von Willebrand factor (VWF; MIM 613160) and mediate the adhesion of platelets to injured vascular surfaces in the arterial circulation, a critical initiating event in hemostasis. The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9; MIM 173515) and GP5. Mutations in GP1BA, GP1BB, and GP9 have been shown to cause Bernard-Soulier syndrome (MIM 231200), a bleeding disorder (review by Lopez et al., 1998 [PubMed 9616133]).[supplied by OMIM, Nov 2010]","start":194394821,"end":194398354,"strand":-1,"description":"glycoprotein V platelet [Source:HGNC Symbol;Acc:HGNC:4443]"}, {"versioned_ensembl_gene_id":"ENSG00000250080.1","gene_symbol":"AC011416.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127170535,"end":127172266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177932.6","gene_symbol":"ZNF354C","gene_name":"zinc finger protein 354C [Source:HGNC Symbol;Acc:HGNC:16736]","synonyms":"KID3","biotype":"protein_coding","ncbi_id":"30832","summary":null,"start":179060415,"end":179083537,"strand":1,"description":"zinc finger protein 354C [Source:HGNC Symbol;Acc:HGNC:16736]"}, {"versioned_ensembl_gene_id":"ENSG00000253911.1","gene_symbol":"AP003467.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98603253,"end":98606340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253468.1","gene_symbol":"AP003355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98412882,"end":98413784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184925.11","gene_symbol":"LCN12","gene_name":"lipocalin 12 [Source:HGNC Symbol;Acc:HGNC:28733]","synonyms":"MGC48935","biotype":"protein_coding","ncbi_id":"286256","summary":"Members of the lipocalin family, such as LCN12, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":136949551,"end":136955497,"strand":1,"description":"lipocalin 12 [Source:HGNC Symbol;Acc:HGNC:28733]"}, {"versioned_ensembl_gene_id":"ENSG00000273047.1","gene_symbol":"AL121845.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63738270,"end":63740398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257296.1","gene_symbol":"AC093027.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84671598,"end":84672026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213228.5","gene_symbol":"RPL12P38","gene_name":"ribosomal protein L12 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36838]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645688","summary":null,"start":60433678,"end":60435996,"strand":-1,"description":"ribosomal protein L12 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36838]"}, {"versioned_ensembl_gene_id":"ENSG00000197253.13","gene_symbol":"TPSB2","gene_name":"tryptase beta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14120]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64499","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. These genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. The alleles of this gene exhibit an unusual amount of sequence variation, such that the alleles were once thought to represent two separate genes, beta II and beta III. Beta tryptases appear to be the main isoenzymes expressed in mast cells, whereas in basophils, alpha-tryptases predominate. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq, Jul 2008]","start":1227272,"end":1230184,"strand":-1,"description":"tryptase beta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14120]"}, {"versioned_ensembl_gene_id":"ENSG00000232886.1","gene_symbol":"AF212831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16862875,"end":16873691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266489.1","gene_symbol":"AC007922.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24516883,"end":24518006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278801.3","gene_symbol":"IGHD","gene_name":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]","synonyms":"MGC29633,FLJ46727,FLJ00382","biotype":"IG_C_gene","ncbi_id":"3495","summary":null,"start":105837536,"end":105846448,"strand":-1,"description":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]"}, {"versioned_ensembl_gene_id":"ENSG00000233287.1","gene_symbol":"AC009362.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131242590,"end":131242995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249990.1","gene_symbol":"MTCO2P24","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075193","summary":null,"start":98409675,"end":98410100,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52153]"}, {"versioned_ensembl_gene_id":"ENSG00000160051.11","gene_symbol":"IQCC","gene_name":"IQ motif containing C [Source:HGNC Symbol;Acc:HGNC:25545]","synonyms":"FLJ10547","biotype":"protein_coding","ncbi_id":"55721","summary":null,"start":32205661,"end":32208687,"strand":1,"description":"IQ motif containing C [Source:HGNC Symbol;Acc:HGNC:25545]"}, {"versioned_ensembl_gene_id":"ENSG00000172014.12","gene_symbol":"ANKRD20A4","gene_name":"ankyrin repeat domain 20 family member A4 [Source:HGNC Symbol;Acc:HGNC:31982]","synonyms":"OTTHUMG00000066855","biotype":"protein_coding","ncbi_id":"728747","summary":null,"start":64369394,"end":64413142,"strand":1,"description":"ankyrin repeat domain 20 family member A4 [Source:HGNC Symbol;Acc:HGNC:31982]"}, {"versioned_ensembl_gene_id":"ENSG00000231721.6","gene_symbol":"LINC-PINT","gene_name":"long intergenic non-protein coding RNA, p53 induced transcript [Source:HGNC Symbol;Acc:HGNC:26885]","synonyms":"PINT,MKLN1-AS1,LincRNA-Pint,FLJ43663","biotype":"antisense_RNA","ncbi_id":"378805","summary":null,"start":130941760,"end":131110176,"strand":-1,"description":"long intergenic non-protein coding RNA, p53 induced transcript [Source:HGNC Symbol;Acc:HGNC:26885]"}, {"versioned_ensembl_gene_id":"ENSG00000223752.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30616685,"end":30636664,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000106688.11","gene_symbol":"SLC1A1","gene_name":"solute carrier family 1 member 1 [Source:HGNC Symbol;Acc:HGNC:10939]","synonyms":"EAAT3,EAAC1","biotype":"protein_coding","ncbi_id":"6505","summary":"This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]","start":4490444,"end":4587469,"strand":1,"description":"solute carrier family 1 member 1 [Source:HGNC Symbol;Acc:HGNC:10939]"}, {"versioned_ensembl_gene_id":"ENSG00000271328.1","gene_symbol":"B3GNTL1P2","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51318]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480419","summary":null,"start":47368943,"end":47369230,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51318]"}, {"versioned_ensembl_gene_id":"ENSG00000102271.13","gene_symbol":"KLHL4","gene_name":"kelch like family member 4 [Source:HGNC Symbol;Acc:HGNC:6355]","synonyms":"KIAA1687,KHL4,DKELCHL","biotype":"protein_coding","ncbi_id":"56062","summary":"This gene encodes a member of the kelch family of proteins, which are characterized by kelch repeat motifs and a POZ/BTB protein-binding domain. It is thought that kelch repeats are actin binding domains. However, the specific function of this protein has not been determined. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":87517749,"end":87670050,"strand":1,"description":"kelch like family member 4 [Source:HGNC Symbol;Acc:HGNC:6355]"}, {"versioned_ensembl_gene_id":"ENSG00000151322.18","gene_symbol":"NPAS3","gene_name":"neuronal PAS domain protein 3 [Source:HGNC Symbol;Acc:HGNC:19311]","synonyms":"PASD6,MOP6,bHLHe12","biotype":"protein_coding","ncbi_id":"64067","summary":"This gene encodes a member of the basic helix-loop-helix and PAS domain-containing family of transcription factors. The encoded protein is localized to the nucleus and may regulate genes involved in neurogenesis. Chromosomal abnormalities that affect the coding potential of this gene are associated with schizophrenia and cognitive disability. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":32934933,"end":33804176,"strand":1,"description":"neuronal PAS domain protein 3 [Source:HGNC Symbol;Acc:HGNC:19311]"}, {"versioned_ensembl_gene_id":"ENSG00000261292.2","gene_symbol":"AC110491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97759523,"end":97761532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250331.1","gene_symbol":"LINC01340","gene_name":"long intergenic non-protein coding RNA 1340 [Source:HGNC Symbol;Acc:HGNC:50550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546227","summary":null,"start":97504696,"end":97671046,"strand":1,"description":"long intergenic non-protein coding RNA 1340 [Source:HGNC Symbol;Acc:HGNC:50550]"}, {"versioned_ensembl_gene_id":"ENSG00000250125.1","gene_symbol":"LINC02232","gene_name":"long intergenic non-protein coding RNA 2232 [Source:HGNC Symbol;Acc:HGNC:53103]","synonyms":"RP11-707A18.1","biotype":"lincRNA","ncbi_id":"401134","summary":null,"start":64914281,"end":65004500,"strand":-1,"description":"long intergenic non-protein coding RNA 2232 [Source:HGNC Symbol;Acc:HGNC:53103]"}, {"versioned_ensembl_gene_id":"ENSG00000244669.1","gene_symbol":"AC104689.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64767130,"end":64767897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248328.1","gene_symbol":"MTCO3P28","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52131]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075184","summary":null,"start":64611374,"end":64611888,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52131]"}, {"versioned_ensembl_gene_id":"ENSG00000132376.19","gene_symbol":"INPP5K","gene_name":"inositol polyphosphate-5-phosphatase K [Source:HGNC Symbol;Acc:HGNC:33882]","synonyms":"SKIP","biotype":"protein_coding","ncbi_id":"51763","summary":"This gene encodes a protein with 5-phosphatase activity toward polyphosphate inositol. The protein localizes to the cytosol in regions lacking actin stress fibers. It is thought that this protein may negatively regulate the actin cytoskeleton. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]","start":1494571,"end":1516888,"strand":-1,"description":"inositol polyphosphate-5-phosphatase K [Source:HGNC Symbol;Acc:HGNC:33882]"}, {"versioned_ensembl_gene_id":"ENSG00000115091.11","gene_symbol":"ACTR3","gene_name":"ARP3 actin related protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:170]","synonyms":"ARP3","biotype":"protein_coding","ncbi_id":"10096","summary":"The specific function of this gene has not yet been determined; however, the protein it encodes is known to be a major constituent of the ARP2/3 complex. This complex is located at the cell surface and is essential to cell shape and motility through lamellipodial actin assembly and protrusion. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":113889960,"end":113962596,"strand":1,"description":"ARP3 actin related protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:170]"}, {"versioned_ensembl_gene_id":"ENSG00000180155.19","gene_symbol":"LYNX1","gene_name":"Ly6/neurotoxin 1 [Source:HGNC Symbol;Acc:HGNC:29604]","synonyms":"SLURP2,SLURP2","biotype":"protein_coding","ncbi_id":"66004","summary":"This gene encodes a GPI-anchored, cell membrane bound member of the Ly6/uPAR (LU) superfamily of proteins containing the unique three-finger LU domain. This protein interacts with nicotinic acetylcholine receptors (nAChRs), and is thought to function as a modulator of nAChR activity to prevent excessive excitation. Alternatively spliced transcript variants have been found for this gene. Read-through transcription between this gene and the neighboring downstream gene (SLURP2) generates naturally-occurring transcripts (LYNX1-SLURP2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Sep 2017]","start":142771197,"end":142777810,"strand":-1,"description":"Ly6/neurotoxin 1 [Source:HGNC Symbol;Acc:HGNC:29604]"}, {"versioned_ensembl_gene_id":"ENSG00000253196.1","gene_symbol":"AC083841.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142763116,"end":142766427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169180.11","gene_symbol":"XPO6","gene_name":"exportin 6 [Source:HGNC Symbol;Acc:HGNC:19733]","synonyms":"RANBP20,KIAA0370,FLJ22519","biotype":"protein_coding","ncbi_id":"23214","summary":"The protein encoded by this gene is a member of the importin-beta family. Members of this family are regulated by the GTPase Ran to mediate transport of cargo across the nuclear envelope. This protein has been shown to mediate nuclear export of profilin-actin complexes. A pseudogene of this gene is located on the long arm of chromosome 14. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":28097979,"end":28211920,"strand":-1,"description":"exportin 6 [Source:HGNC Symbol;Acc:HGNC:19733]"}, {"versioned_ensembl_gene_id":"ENSG00000271626.1","gene_symbol":"AC104763.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60315834,"end":60316215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116984.12","gene_symbol":"MTR","gene_name":"5-methyltetrahydrofolate-homocysteine methyltransferase [Source:HGNC Symbol;Acc:HGNC:7468]","synonyms":"cblG","biotype":"protein_coding","ncbi_id":"4548","summary":"This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":236795281,"end":236903981,"strand":1,"description":"5-methyltetrahydrofolate-homocysteine methyltransferase [Source:HGNC Symbol;Acc:HGNC:7468]"}, {"versioned_ensembl_gene_id":"ENSG00000230533.2","gene_symbol":"AL357060.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137673378,"end":137763984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116786.11","gene_symbol":"PLEKHM2","gene_name":"pleckstrin homology and RUN domain containing M2 [Source:HGNC Symbol;Acc:HGNC:29131]","synonyms":"KIAA0842","biotype":"protein_coding","ncbi_id":"23207","summary":"This gene encodes a protein that binds the plus-end directed microtubule motor protein kinesin, together with the lysosomal GTPase Arl8, and is required for lysosomes to distribute away from the microtubule-organizing center. The encoded protein belongs to the multisubunit BLOC-one-related complex that regulates lysosome positioning. It binds a Salmonella effector protein called Salmonella induced filament A and is a critical host determinant in Salmonella pathogenesis. It has a domain architecture consisting of an N-terminal RPIP8, UNC-14, and NESCA (RUN) domain that binds kinesin-1 as well as the lysosomal GTPase Arl8, and a C-terminal pleckstrin homology domain that binds the Salmonella induced filament A effector protein. Naturally occurring mutations in this gene lead to abnormal localization of lysosomes, impaired autophagy flux and are associated with recessive dilated cardiomyopathy and left ventricular noncompaction. [provided by RefSeq, Feb 2017]","start":15684332,"end":15734769,"strand":1,"description":"pleckstrin homology and RUN domain containing M2 [Source:HGNC Symbol;Acc:HGNC:29131]"}, {"versioned_ensembl_gene_id":"ENSG00000143815.14","gene_symbol":"LBR","gene_name":"lamin B receptor [Source:HGNC Symbol;Acc:HGNC:6518]","synonyms":"TDRD18,DHCR14B","biotype":"protein_coding","ncbi_id":"3930","summary":"The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":225401502,"end":225428925,"strand":-1,"description":"lamin B receptor [Source:HGNC Symbol;Acc:HGNC:6518]"}, {"versioned_ensembl_gene_id":"ENSG00000281649.1","gene_symbol":"EBLN3P","gene_name":"endogenous Bornavirus-like nucleoprotein 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:50682]","synonyms":"LOC100506710,EBLN3","biotype":"lincRNA","ncbi_id":"100506710","summary":null,"start":37079857,"end":37090507,"strand":1,"description":"endogenous Bornavirus-like nucleoprotein 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:50682]"}, {"versioned_ensembl_gene_id":"ENSG00000229996.1","gene_symbol":"AC093585.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241010045,"end":241010744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277532.1","gene_symbol":"AC025048.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60124110,"end":60125474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274220.1","gene_symbol":"AC009163.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75433836,"end":75436392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111144.9","gene_symbol":"LTA4H","gene_name":"leukotriene A4 hydrolase [Source:HGNC Symbol;Acc:HGNC:6710]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4048","summary":"The protein encoded by this gene is an enzyme that contains both hydrolase and aminopeptidase activities. The hydrolase activity is used in the final step of the biosynthesis of leukotriene B4, a proinflammatory mediator. The aminopeptidase activity has been shown to degrade proline-glycine-proline (PGP), a neutrophil chemoattractant and biomarker for chronic obstructive pulmonary disease (COPD). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":96000828,"end":96043520,"strand":-1,"description":"leukotriene A4 hydrolase [Source:HGNC Symbol;Acc:HGNC:6710]"}, {"versioned_ensembl_gene_id":"ENSG00000257715.1","gene_symbol":"AC007298.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96025323,"end":96027971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166889.13","gene_symbol":"PATL1","gene_name":"PAT1 homolog 1, processing body mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:26721]","synonyms":"Pat1b,FLJ36874","biotype":"protein_coding","ncbi_id":"219988","summary":null,"start":59636716,"end":59668980,"strand":-1,"description":"PAT1 homolog 1, processing body mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:26721]"}, {"versioned_ensembl_gene_id":"ENSG00000134684.10","gene_symbol":"YARS","gene_name":"tyrosyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12840]","synonyms":"YTS,YRS,tyrRS","biotype":"protein_coding","ncbi_id":"8565","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Tyrosyl-tRNA synthetase belongs to the class I tRNA synthetase family. Cytokine activities have also been observed for the human tyrosyl-tRNA synthetase, after it is split into two parts, an N-terminal fragment that harbors the catalytic site and a C-terminal fragment found only in the mammalian enzyme. The N-terminal fragment is an interleukin-8-like cytokine, whereas the released C-terminal fragment is an EMAP II-like cytokine. [provided by RefSeq, Jul 2008]","start":32775237,"end":32818153,"strand":-1,"description":"tyrosyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12840]"}, {"versioned_ensembl_gene_id":"ENSG00000071564.14","gene_symbol":"TCF3","gene_name":"transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11633]","synonyms":"VDIR,MGC129648,MGC129647,ITF1,E47,E2A,bHLHb21","biotype":"protein_coding","ncbi_id":"6929","summary":"This gene encodes a member of the E protein (class I) family of helix-loop-helix transcription factors. E proteins activate transcription by binding to regulatory E-box sequences on target genes as heterodimers or homodimers, and are inhibited by heterodimerization with inhibitor of DNA-binding (class IV) helix-loop-helix proteins. E proteins play a critical role in lymphopoiesis, and the encoded protein is required for B and T lymphocyte development. Deletion of this gene or diminished activity of the encoded protein may play a role in lymphoid malignancies. This gene is also involved in several chromosomal translocations that are associated with lymphoid malignancies including pre-B-cell acute lymphoblastic leukemia (t(1;19), with PBX1), childhood leukemia (t(19;19), with TFPT) and acute leukemia (t(12;19), with ZNF384). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Sep 2011]","start":1609290,"end":1652605,"strand":-1,"description":"transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11633]"}, {"versioned_ensembl_gene_id":"ENSG00000227306.1","gene_symbol":"AP006285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1688297,"end":1689056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107537.13","gene_symbol":"PHYH","gene_name":"phytanoyl-CoA 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:8940]","synonyms":"RD,PHYH1,PAHX","biotype":"protein_coding","ncbi_id":"5264","summary":"This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":13277796,"end":13302412,"strand":-1,"description":"phytanoyl-CoA 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:8940]"}, {"versioned_ensembl_gene_id":"ENSG00000258957.1","gene_symbol":"AL359317.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69183020,"end":69214092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136286.14","gene_symbol":"MYO1G","gene_name":"myosin IG [Source:HGNC Symbol;Acc:HGNC:13880]","synonyms":"HA-2","biotype":"protein_coding","ncbi_id":"64005","summary":"MYO1G is a plasma membrane-associated class I myosin (see MIM 601478) that is abundant in T and B lymphocytes and mast cells (Pierce et al., 2001 [PubMed 11544309]; Patino-Lopez et al., 2010 [PubMed 20071333]).[supplied by OMIM, Jun 2010]","start":44962662,"end":44979098,"strand":-1,"description":"myosin IG [Source:HGNC Symbol;Acc:HGNC:13880]"}, {"versioned_ensembl_gene_id":"ENSG00000166670.9","gene_symbol":"MMP10","gene_name":"matrix metallopeptidase 10 [Source:HGNC Symbol;Acc:HGNC:7156]","synonyms":"STMY2","biotype":"protein_coding","ncbi_id":"4319","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down fibronectin, laminin, elastin, proteoglycan core protein, gelatins, and several types of collagen. The gene is part of a cluster of MMP genes on chromosome 11. [provided by RefSeq, Jan 2016]","start":102770503,"end":102780628,"strand":-1,"description":"matrix metallopeptidase 10 [Source:HGNC Symbol;Acc:HGNC:7156]"}, {"versioned_ensembl_gene_id":"ENSG00000113100.9","gene_symbol":"CDH9","gene_name":"cadherin 9 [Source:HGNC Symbol;Acc:HGNC:1768]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1007","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. The extracellular domain consists of 5 subdomains, each containing a cadherin motif, and appears to determine the specificity of the protein's homophilic cell adhesion activity. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. [provided by RefSeq, Jul 2008]","start":26880600,"end":27121150,"strand":-1,"description":"cadherin 9 [Source:HGNC Symbol;Acc:HGNC:1768]"}, {"versioned_ensembl_gene_id":"ENSG00000183798.4","gene_symbol":"EMILIN3","gene_name":"elastin microfibril interfacer 3 [Source:HGNC Symbol;Acc:HGNC:16123]","synonyms":"EMILIN5,dJ620E11.4,C20orf130","biotype":"protein_coding","ncbi_id":"90187","summary":null,"start":41359966,"end":41366827,"strand":-1,"description":"elastin microfibril interfacer 3 [Source:HGNC Symbol;Acc:HGNC:16123]"}, {"versioned_ensembl_gene_id":"ENSG00000225360.1","gene_symbol":"AL772155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63729702,"end":63730173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253140.1","gene_symbol":"AC026904.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48515852,"end":48517089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257529.5","gene_symbol":"RPL36A-HNRNPH2","gene_name":"RPL36A-HNRNPH2 readthrough [Source:HGNC Symbol;Acc:HGNC:48349]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529097","summary":"This locus represents naturally occurring read-through transcription between the neighboring ribosomal protein L36a and heterogeneous nuclear ribonucleoprotein H2 (H') genes on chromosome X. The read-through transcript produces a protein with similarity to the protein encoded by the upstream locus, ribosomal protein L36a. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jan 2011]","start":101391011,"end":101412297,"strand":1,"description":"RPL36A-HNRNPH2 readthrough [Source:HGNC Symbol;Acc:HGNC:48349]"}, {"versioned_ensembl_gene_id":"ENSG00000226343.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32770986,"end":32771923,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000268049.1","gene_symbol":"AC012313.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58357999,"end":58359603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261460.1","gene_symbol":"AC009690.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72278867,"end":72351794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254770.1","gene_symbol":"OR4D7P","gene_name":"olfactory receptor family 4 subfamily D member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15176]","synonyms":"OST724","biotype":"unprocessed_pseudogene","ncbi_id":"81304","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59531754,"end":59532695,"strand":1,"description":"olfactory receptor family 4 subfamily D member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15176]"}, {"versioned_ensembl_gene_id":"ENSG00000228674.4","gene_symbol":"AC011483.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50927079,"end":50927571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228763.1","gene_symbol":"LIMS1-AS1","gene_name":"LIMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40342]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106182118","summary":null,"start":108676795,"end":108678601,"strand":-1,"description":"LIMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40342]"}, {"versioned_ensembl_gene_id":"ENSG00000277342.1","gene_symbol":"AC048344.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32109076,"end":32109602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160886.13","gene_symbol":"LY6K","gene_name":"lymphocyte antigen 6 family member K [Source:HGNC Symbol;Acc:HGNC:24225]","synonyms":"HSJ001348,FLJ35226,CT97","biotype":"protein_coding","ncbi_id":"54742","summary":null,"start":142700111,"end":142705127,"strand":1,"description":"lymphocyte antigen 6 family member K [Source:HGNC Symbol;Acc:HGNC:24225]"}, {"versioned_ensembl_gene_id":"ENSG00000119514.6","gene_symbol":"GALNT12","gene_name":"polypeptide N-acetylgalactosaminyltransferase 12 [Source:HGNC Symbol;Acc:HGNC:19877]","synonyms":"GalNAc-T12","biotype":"protein_coding","ncbi_id":"79695","summary":"This gene encodes a member of a family of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferases, which catalyze the transfer of N-acetylgalactosamine (GalNAc) from UDP-GalNAc to a serine or threonine residue on a polypeptide acceptor in the initial step of O-linked protein glycosylation. Mutations in this gene are associated with an increased susceptibility to colorectal cancer.[provided by RefSeq, Mar 2011]","start":98807699,"end":98850081,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 12 [Source:HGNC Symbol;Acc:HGNC:19877]"}, {"versioned_ensembl_gene_id":"ENSG00000249761.1","gene_symbol":"AC074133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97336858,"end":97337040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244234.1","gene_symbol":"GMCL1P1","gene_name":"germ cell-less, spermatogenesis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19717]","synonyms":"GMCL1L,GCL,GMCL2","biotype":"processed_pseudogene","ncbi_id":"64396","summary":"This locus shares a high degree of identity with the multi-exon germ cell-less gene on chromosome 2. Despite its single-exon nature, this chromosome 5 locus contains an open reading frame that could putatively encode a full-length germ cell-less related protein. [provided by RefSeq, Jul 2008]","start":178185719,"end":178187299,"strand":-1,"description":"germ cell-less, spermatogenesis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19717]"}, {"versioned_ensembl_gene_id":"ENSG00000254502.1","gene_symbol":"AP003097.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86195132,"end":86196266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213630.3","gene_symbol":"BOLA3P3","gene_name":"bolA family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644754","summary":null,"start":126663337,"end":126663568,"strand":-1,"description":"bolA family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51442]"}, {"versioned_ensembl_gene_id":"ENSG00000172320.3","gene_symbol":"OR5A1","gene_name":"olfactory receptor family 5 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8319]","synonyms":"OST181,OR5A1P","biotype":"protein_coding","ncbi_id":"219982","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59436469,"end":59451380,"strand":1,"description":"olfactory receptor family 5 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8319]"}, {"versioned_ensembl_gene_id":"ENSG00000100036.12","gene_symbol":"SLC35E4","gene_name":"solute carrier family 35 member E4 [Source:HGNC Symbol;Acc:HGNC:17058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339665","summary":null,"start":30635652,"end":30669016,"strand":1,"description":"solute carrier family 35 member E4 [Source:HGNC Symbol;Acc:HGNC:17058]"}, {"versioned_ensembl_gene_id":"ENSG00000250318.1","gene_symbol":"AC003072.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30653877,"end":30654814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186369.10","gene_symbol":"LINC00643","gene_name":"long intergenic non-protein coding RNA 643 [Source:HGNC Symbol;Acc:HGNC:44296]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"646113","summary":null,"start":62114353,"end":62130962,"strand":1,"description":"long intergenic non-protein coding RNA 643 [Source:HGNC Symbol;Acc:HGNC:44296]"}, {"versioned_ensembl_gene_id":"ENSG00000257431.1","gene_symbol":"AC089998.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82512677,"end":82515817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281982.1","gene_symbol":"AC003070.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45396932,"end":45397477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124610.4","gene_symbol":"HIST1H1A","gene_name":"histone cluster 1 H1 family member a [Source:HGNC Symbol;Acc:HGNC:4715]","synonyms":"H1F1,H1a,H1.1","biotype":"protein_coding","ncbi_id":"3024","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26017085,"end":26017732,"strand":-1,"description":"histone cluster 1 H1 family member a [Source:HGNC Symbol;Acc:HGNC:4715]"}, {"versioned_ensembl_gene_id":"ENSG00000077522.12","gene_symbol":"ACTN2","gene_name":"actinin alpha 2 [Source:HGNC Symbol;Acc:HGNC:164]","synonyms":null,"biotype":"protein_coding","ncbi_id":"88","summary":"Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a muscle-specific, alpha actinin isoform that is expressed in both skeletal and cardiac muscles. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]","start":236686454,"end":236764631,"strand":1,"description":"actinin alpha 2 [Source:HGNC Symbol;Acc:HGNC:164]"}, {"versioned_ensembl_gene_id":"ENSG00000165138.17","gene_symbol":"ANKS6","gene_name":"ankyrin repeat and sterile alpha motif domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26724]","synonyms":"SAMD6,NPHP16,FLJ36928,ANKRD14","biotype":"protein_coding","ncbi_id":"203286","summary":"This gene encodes a protein containing multiple ankyrin repeats and a SAM domain. It is thought that this protein may localize to the proximal region of the primary cilium, and may play a role in renal and cardiovascular development. Mutations in this gene have been shown to cause a form of nephronophthisis (NPHP16), a chronic tubulo-interstitial nephritis. [provided by RefSeq, Jul 2015]","start":98731329,"end":98796965,"strand":-1,"description":"ankyrin repeat and sterile alpha motif domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26724]"}, {"versioned_ensembl_gene_id":"ENSG00000279900.1","gene_symbol":"AP001767.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":83083687,"end":83084138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254660.1","gene_symbol":"AP002512.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56509573,"end":56510195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213760.10","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G2,NG38,ATP6G,Em:AC004181.3,Vma10","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31544462,"end":31548427,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000234423.1","gene_symbol":"LINC01250","gene_name":"long intergenic non-protein coding RNA 1250 [Source:HGNC Symbol;Acc:HGNC:49844]","synonyms":"FLJ37991","biotype":"lincRNA","ncbi_id":"101927554","summary":null,"start":2895048,"end":3126026,"strand":-1,"description":"long intergenic non-protein coding RNA 1250 [Source:HGNC Symbol;Acc:HGNC:49844]"}, {"versioned_ensembl_gene_id":"ENSG00000267104.2","gene_symbol":"TBC1D3P1-DHX40P1","gene_name":"TBC1D3P1-DHX40P1 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42362]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"653645","summary":"This locus represents naturally-occurring readthrough transcription that extends through two unprocessed pseudogenes, TBC1D3P1 (TBC1 domain family member 3 pseudogene 1) and DHX40P1 (DEAH-box helicase 40 pseudogene 1), to protein-coding RNFT1 (ring finger protein, transmembrane 1). The individual pseudogene loci are not curated as transcribed regions. The readthrough transcript likely does not encode a functional protein, since translation of the long open reading frames would render the transcript a candidate for nonsense-mediated decay (NMD). [provided by RefSeq, Jan 2016]","start":59962363,"end":60018975,"strand":-1,"description":"TBC1D3P1-DHX40P1 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42362]"}, {"versioned_ensembl_gene_id":"ENSG00000266265.2","gene_symbol":"KLF14","gene_name":"Kruppel like factor 14 [Source:HGNC Symbol;Acc:HGNC:23025]","synonyms":"BTEB5","biotype":"protein_coding","ncbi_id":"136259","summary":"This intronless gene encodes a member of the Kruppel-like family of transcription factors. The encoded protein functions as a transcriptional co-repressor, and is induced by transforming growth factor-beta (TGF-beta) to repress TGF-beta receptor II gene expression. This gene exhibits imprinted expression from the maternal allele in embryonic and extra-embryonic tissues. [provided by RefSeq, Jul 2013]","start":130731235,"end":130734061,"strand":-1,"description":"Kruppel like factor 14 [Source:HGNC Symbol;Acc:HGNC:23025]"}, {"versioned_ensembl_gene_id":"ENSG00000265190.6","gene_symbol":"ANXA8","gene_name":"annexin A8 [Source:HGNC Symbol;Acc:HGNC:546]","synonyms":"ANX8","biotype":"protein_coding","ncbi_id":"653145","summary":"This gene encodes a member of the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins. The encoded protein may function as an an anticoagulant that indirectly inhibits the thromboplastin-specific complex. Overexpression of this gene has been associated with acute myelocytic leukemia. A highly similar duplicated copy of this gene is found in close proximity on the long arm of chromosome 10. [provided by RefSeq, Jul 2008]","start":47460162,"end":47484158,"strand":-1,"description":"annexin A8 [Source:HGNC Symbol;Acc:HGNC:546]"}, {"versioned_ensembl_gene_id":"ENSG00000172057.9","gene_symbol":"ORMDL3","gene_name":"ORMDL sphingolipid biosynthesis regulator 3 [Source:HGNC Symbol;Acc:HGNC:16038]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94103","summary":null,"start":39921041,"end":39927601,"strand":-1,"description":"ORMDL sphingolipid biosynthesis regulator 3 [Source:HGNC Symbol;Acc:HGNC:16038]"}, {"versioned_ensembl_gene_id":"ENSG00000225087.1","gene_symbol":"AL583808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72748921,"end":72899140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132446.6","gene_symbol":"FTHL17","gene_name":"ferritin heavy chain like 17 [Source:HGNC Symbol;Acc:HGNC:3987]","synonyms":"CT38","biotype":"protein_coding","ncbi_id":"53940","summary":"This gene encodes a ferritin heavy chain-like protein. This gene is primarily expressed in embryonic germ cells. The encoded protein may lack ferroxidase activity. Multiple pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Oct 2016]","start":31071241,"end":31072053,"strand":-1,"description":"ferritin heavy chain like 17 [Source:HGNC Symbol;Acc:HGNC:3987]"}, {"versioned_ensembl_gene_id":"ENSG00000232235.1","gene_symbol":"CDY3P","gene_name":"chromodomain Y-linked 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:23849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286556","summary":null,"start":9166085,"end":9167702,"strand":-1,"description":"chromodomain Y-linked 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:23849]"}, {"versioned_ensembl_gene_id":"ENSG00000271314.1","gene_symbol":"AL161729.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95494924,"end":95495379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227364.1","gene_symbol":"AC018685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2729908,"end":2730957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231988.1","gene_symbol":"OFD1P3Y","gene_name":"OFD1 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:23875]","synonyms":"OFDYP3,OFD1PY3,OFD1PY19,OFD1P3,OFD1P19Y,OFD1P19","biotype":"unprocessed_pseudogene","ncbi_id":"386687","summary":null,"start":9030594,"end":9039988,"strand":1,"description":"OFD1 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:23875]"}, {"versioned_ensembl_gene_id":"ENSG00000226127.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"HSBLMHC1,BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32460601,"end":32473766,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000276925.1","gene_symbol":"AC099778.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47469777,"end":47469987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166313.18","gene_symbol":"APBB1","gene_name":"amyloid beta precursor protein binding family B member 1 [Source:HGNC Symbol;Acc:HGNC:581]","synonyms":"RIR,Fe65","biotype":"protein_coding","ncbi_id":"322","summary":"The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid precursor protein (APP), transcription factor CP2/LSF/LBP1 and the low-density lipoprotein receptor-related protein. APP functions as a cytosolic anchoring site that can prevent the gene product's nuclear translocation. This encoded protein could play an important role in the pathogenesis of Alzheimer's disease. It is thought to regulate transcription. Also it is observed to block cell cycle progression by downregulating thymidylate synthase expression. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012]","start":6395124,"end":6419414,"strand":-1,"description":"amyloid beta precursor protein binding family B member 1 [Source:HGNC Symbol;Acc:HGNC:581]"}, {"versioned_ensembl_gene_id":"ENSG00000267028.1","gene_symbol":"TCF4-AS1","gene_name":"TCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51642]","synonyms":"MIR4529HG","biotype":"antisense_RNA","ncbi_id":"105372127","summary":null,"start":55452533,"end":55482940,"strand":1,"description":"TCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51642]"}, {"versioned_ensembl_gene_id":"ENSG00000242320.2","gene_symbol":"RPL21P126","gene_name":"ribosomal protein L21 pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:35959]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271449","summary":null,"start":55635833,"end":55636310,"strand":1,"description":"ribosomal protein L21 pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:35959]"}, {"versioned_ensembl_gene_id":"ENSG00000146433.8","gene_symbol":"TMEM181","gene_name":"transmembrane protein 181 [Source:HGNC Symbol;Acc:HGNC:20958]","synonyms":"KIAA1423,GPR178","biotype":"protein_coding","ncbi_id":"57583","summary":"The TMEM181 gene encodes a putative G protein-coupled receptor expressed on the cell surface (Carette et al., 2009 [PubMed 19965467]; Wollscheid et al., 2009 [PubMed 19349973]).[supplied by OMIM, Jan 2010]","start":158536436,"end":158635428,"strand":1,"description":"transmembrane protein 181 [Source:HGNC Symbol;Acc:HGNC:20958]"}, {"versioned_ensembl_gene_id":"ENSG00000091138.12","gene_symbol":"SLC26A3","gene_name":"solute carrier family 26 member 3 [Source:HGNC Symbol;Acc:HGNC:3018]","synonyms":"DRA,CLD","biotype":"protein_coding","ncbi_id":"1811","summary":"The protein encoded by this gene is a transmembrane glycoprotein that transports chloride ions across the cell membrane in exchange for bicarbonate ions. It is localized to the mucosa of the lower intestinal tract, particularly to the apical membrane of columnar epithelium and some goblet cells. The protein is essential for intestinal chloride absorption, and mutations in this gene have been associated with congenital chloride diarrhea. [provided by RefSeq, Oct 2008]","start":107765467,"end":107803225,"strand":-1,"description":"solute carrier family 26 member 3 [Source:HGNC Symbol;Acc:HGNC:3018]"}, {"versioned_ensembl_gene_id":"ENSG00000179997.8","gene_symbol":"AC010894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174501952,"end":174502312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164463.12","gene_symbol":"CREBRF","gene_name":"CREB3 regulatory factor [Source:HGNC Symbol;Acc:HGNC:24050]","synonyms":"LRF,C5orf41","biotype":"protein_coding","ncbi_id":"153222","summary":null,"start":173056352,"end":173139284,"strand":1,"description":"CREB3 regulatory factor [Source:HGNC Symbol;Acc:HGNC:24050]"}, {"versioned_ensembl_gene_id":"ENSG00000227078.1","gene_symbol":"LINC02094","gene_name":"long intergenic non-protein coding RNA 2094 [Source:HGNC Symbol;Acc:HGNC:52945]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984995","summary":null,"start":19419035,"end":19424357,"strand":1,"description":"long intergenic non-protein coding RNA 2094 [Source:HGNC Symbol;Acc:HGNC:52945]"}, {"versioned_ensembl_gene_id":"ENSG00000231477.2","gene_symbol":"AC004448.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19457080,"end":19458399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252690.3","gene_symbol":"SCARNA15","gene_name":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]","synonyms":"ACA45,ACA45","biotype":"processed_transcript","ncbi_id":"677778","summary":null,"start":82752884,"end":82757208,"strand":1,"description":"small Cajal body-specific RNA 15 [Source:HGNC Symbol;Acc:HGNC:32572]"}, {"versioned_ensembl_gene_id":"ENSG00000259753.1","gene_symbol":"AC068234.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":47253897,"end":47344292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259442.1","gene_symbol":"AC105339.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82744223,"end":82750289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186081.11","gene_symbol":"KRT5","gene_name":"keratin 5 [Source:HGNC Symbol;Acc:HGNC:6442]","synonyms":"KRT5A,EBS2","biotype":"protein_coding","ncbi_id":"3852","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52514575,"end":52520687,"strand":-1,"description":"keratin 5 [Source:HGNC Symbol;Acc:HGNC:6442]"}, {"versioned_ensembl_gene_id":"ENSG00000279758.1","gene_symbol":"AC105339.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82738386,"end":82739122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232380.1","gene_symbol":"ZDHHC20P4","gene_name":"zinc finger DHHC-type containing 20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730239","summary":null,"start":68985058,"end":68986064,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39776]"}, {"versioned_ensembl_gene_id":"ENSG00000230405.1","gene_symbol":"RPS3AP52","gene_name":"ribosomal protein S3a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:42004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873818","summary":null,"start":68634190,"end":68634486,"strand":1,"description":"ribosomal protein S3a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:42004]"}, {"versioned_ensembl_gene_id":"ENSG00000225055.1","gene_symbol":"AL606490.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48357125,"end":48359495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188368.9","gene_symbol":"PRR19","gene_name":"proline rich 19 [Source:HGNC Symbol;Acc:HGNC:33728]","synonyms":"MGC70924","biotype":"protein_coding","ncbi_id":"284338","summary":null,"start":42302098,"end":42310821,"strand":1,"description":"proline rich 19 [Source:HGNC Symbol;Acc:HGNC:33728]"}, {"versioned_ensembl_gene_id":"ENSG00000280434.1","gene_symbol":"AL031595.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":44139365,"end":44153626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165584.15","gene_symbol":"SSX3","gene_name":"SSX family member 3 [Source:HGNC Symbol;Acc:HGNC:11337]","synonyms":"CT5.3","biotype":"protein_coding","ncbi_id":"10214","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. While some of the related SSX genes are involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas, this gene does not appear to be involved in such translocations. [provided by RefSeq, Jul 2013]","start":48346428,"end":48356707,"strand":-1,"description":"SSX family member 3 [Source:HGNC Symbol;Acc:HGNC:11337]"}, {"versioned_ensembl_gene_id":"ENSG00000242882.1","gene_symbol":"RPL5P11","gene_name":"ribosomal protein L5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35483]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402193","summary":null,"start":173419245,"end":173420137,"strand":-1,"description":"ribosomal protein L5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35483]"}, {"versioned_ensembl_gene_id":"ENSG00000256100.1","gene_symbol":"AP000721.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63974620,"end":63988346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176340.3","gene_symbol":"COX8A","gene_name":"cytochrome c oxidase subunit 8A [Source:HGNC Symbol;Acc:HGNC:2294]","synonyms":"VIII-L,VIII,COX8L,COX8-2,COX8,COX","biotype":"protein_coding","ncbi_id":"1351","summary":"The protein encoded by this gene is the terminal enzyme of the respiratory chain, coupling the transfer of electrons from cytochrome c to molecular oxygen, with the concomitant production of a proton electrochemical gradient across the inner mitochondrial membrane. In addition to 3 mitochondrially encoded subunits, which perform the catalytic function, the eukaryotic enzyme contains nuclear-encoded smaller subunits, ranging in number from 4 in some organisms to 10 in mammals. It has been proposed that nuclear-encoded subunits may be involved in the modulation of the catalytic function. This gene encodes one of the nuclear-encoded subunits. [provided by RefSeq, Jul 2008]","start":63974607,"end":63976543,"strand":1,"description":"cytochrome c oxidase subunit 8A [Source:HGNC Symbol;Acc:HGNC:2294]"}, {"versioned_ensembl_gene_id":"ENSG00000256341.1","gene_symbol":"AP006333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64118272,"end":64119210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275111.4","gene_symbol":"ZNF2","gene_name":"zinc finger protein 2 [Source:HGNC Symbol;Acc:HGNC:12991]","synonyms":"ZNF661,Zfp661,A1-5","biotype":"protein_coding","ncbi_id":"7549","summary":"The protein encoded by this gene belongs to the C2H2-type zinc-finger protein family. The exact function of this gene is not known, however, zinc-finger proteins are known to interact with DNA and function as transcription regulators. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":95165432,"end":95184317,"strand":1,"description":"zinc finger protein 2 [Source:HGNC Symbol;Acc:HGNC:12991]"}, {"versioned_ensembl_gene_id":"ENSG00000163399.15","gene_symbol":"ATP1A1","gene_name":"ATPase Na+/K+ transporting subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:799]","synonyms":null,"biotype":"protein_coding","ncbi_id":"476","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 1 subunit. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":116372668,"end":116410261,"strand":1,"description":"ATPase Na+/K+ transporting subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:799]"}, {"versioned_ensembl_gene_id":"ENSG00000254267.1","gene_symbol":"AP003438.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98371355,"end":98388247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256249.1","gene_symbol":"AC026333.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122687125,"end":122715979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240520.6","gene_symbol":"UOX","gene_name":"urate oxidase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12575]","synonyms":"UOXP","biotype":"transcribed_unitary_pseudogene","ncbi_id":"391051","summary":"Urate oxidase is an enzyme that catalyzes the oxidation of uric acid to allantoin. This gene has been inactivated by mutation and is nonfunctional in humans and some other primates. [provided by RefSeq, Jul 2008]","start":84363706,"end":84397831,"strand":-1,"description":"urate oxidase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12575]"}, {"versioned_ensembl_gene_id":"ENSG00000110713.15","gene_symbol":"NUP98","gene_name":"nucleoporin 98 [Source:HGNC Symbol;Acc:HGNC:8068]","synonyms":"NUP96","biotype":"protein_coding","ncbi_id":"4928","summary":"Nuclear pore complexes (NPCs) regulate the transport of macromolecules between the nucleus and cytoplasm, and are composed of many polypeptide subunits, many of which belong to the nucleoporin family. This gene belongs to the nucleoporin gene family and encodes a 186 kDa precursor protein that undergoes autoproteolytic cleavage to generate a 98 kDa nucleoporin and 96 kDa nucleoporin. The 98 kDa nucleoporin contains a Gly-Leu-Phe-Gly (GLGF) repeat domain and participates in many cellular processes, including nuclear import, nuclear export, mitotic progression, and regulation of gene expression. The 96 kDa nucleoporin is a scaffold component of the NPC. Proteolytic cleavage is important for targeting of the proteins to the NPC. Translocations between this gene and many other partner genes have been observed in different leukemias. Rearrangements typically result in chimeras with the N-terminal GLGF domain of this gene to the C-terminus of the partner gene. Alternative splicing results in multiple transcript variants encoding different isoforms, at least two of which are proteolytically processed. Some variants lack the region that encodes the 96 kDa nucleoporin. [provided by RefSeq, Feb 2016]","start":3671083,"end":3797792,"strand":-1,"description":"nucleoporin 98 [Source:HGNC Symbol;Acc:HGNC:8068]"}, {"versioned_ensembl_gene_id":"ENSG00000136457.9","gene_symbol":"CHAD","gene_name":"chondroadherin [Source:HGNC Symbol;Acc:HGNC:1909]","synonyms":"SLRR4A","biotype":"protein_coding","ncbi_id":"1101","summary":"Chondroadherin is a cartilage matrix protein thought to mediate adhesion of isolated chondrocytes. The protein contains 11 leucine-rich repeats flanked by cysteine-rich regions. The chondroadherin messenger RNA is present in chondrocytes at all ages. [provided by RefSeq, Jul 2008]","start":50464496,"end":50468966,"strand":-1,"description":"chondroadherin [Source:HGNC Symbol;Acc:HGNC:1909]"}, {"versioned_ensembl_gene_id":"ENSG00000176148.15","gene_symbol":"TCP11L1","gene_name":"t-complex 11 like 1 [Source:HGNC Symbol;Acc:HGNC:25655]","synonyms":"FLJ11336","biotype":"protein_coding","ncbi_id":"55346","summary":null,"start":33039417,"end":33105943,"strand":1,"description":"t-complex 11 like 1 [Source:HGNC Symbol;Acc:HGNC:25655]"}, {"versioned_ensembl_gene_id":"ENSG00000204520.12","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31399784,"end":31415315,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000254993.1","gene_symbol":"TRIM77BP","gene_name":"tripartite motif containing 77B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43980]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646770","summary":null,"start":49117019,"end":49124570,"strand":-1,"description":"tripartite motif containing 77B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43980]"}, {"versioned_ensembl_gene_id":"ENSG00000278308.2","gene_symbol":"NPIPA3","gene_name":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642778","summary":null,"start":14708949,"end":14726344,"strand":1,"description":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]"}, {"versioned_ensembl_gene_id":"ENSG00000104205.12","gene_symbol":"SGK3","gene_name":"serum/glucocorticoid regulated kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:10812]","synonyms":"SGKL,SGK2","biotype":"protein_coding","ncbi_id":"23678","summary":"This gene is a member of the Ser/Thr protein kinase family and encodes a phosphoprotein with a PX (phox homology) domain. The protein phosphorylates several target proteins and has a role in neutral amino acid transport and activation of potassium and chloride channels. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":66712418,"end":66862022,"strand":1,"description":"serum/glucocorticoid regulated kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:10812]"}, {"versioned_ensembl_gene_id":"ENSG00000230350.1","gene_symbol":"RPL35AP3","gene_name":"ribosomal protein L35a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21117]","synonyms":"bA55K22.4","biotype":"processed_pseudogene","ncbi_id":"387074","summary":null,"start":136973930,"end":136974217,"strand":-1,"description":"ribosomal protein L35a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21117]"}, {"versioned_ensembl_gene_id":"ENSG00000223702.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31380411,"end":31380839,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000276623.1","gene_symbol":"AC106872.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165016887,"end":165017433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250887.1","gene_symbol":"AC106872.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165007086,"end":165007959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236399.7","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30214604,"end":30227224,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000259550.2","gene_symbol":"HNRNPA1P74","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:48804]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421430","summary":null,"start":54320731,"end":54321565,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:48804]"}, {"versioned_ensembl_gene_id":"ENSG00000006016.10","gene_symbol":"CRLF1","gene_name":"cytokine receptor like factor 1 [Source:HGNC Symbol;Acc:HGNC:2364]","synonyms":"CLF-1,CLF,CISS1,CISS","biotype":"protein_coding","ncbi_id":"9244","summary":"This gene encodes a member of the cytokine type I receptor family. The protein forms a secreted complex with cardiotrophin-like cytokine factor 1 and acts on cells expressing ciliary neurotrophic factor receptors. The complex can promote survival of neuronal cells. Mutations in this gene result in Crisponi syndrome and cold-induced sweating syndrome. [provided by RefSeq, Oct 2009]","start":18572220,"end":18607741,"strand":-1,"description":"cytokine receptor like factor 1 [Source:HGNC Symbol;Acc:HGNC:2364]"}, {"versioned_ensembl_gene_id":"ENSG00000274198.1","gene_symbol":"AC025521.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58747055,"end":58747340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276717.1","gene_symbol":"AL136097.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92177235,"end":92188652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121089.4","gene_symbol":"NACA3P","gene_name":"NACA family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33442]","synonyms":"NACA3","biotype":"processed_pseudogene","ncbi_id":"389240","summary":null,"start":164943290,"end":164943937,"strand":1,"description":"NACA family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33442]"}, {"versioned_ensembl_gene_id":"ENSG00000236164.1","gene_symbol":"AL161618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46758296,"end":46761158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245571.6","gene_symbol":"AP001258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59130133,"end":59143015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236438.7","gene_symbol":"FAM157A","gene_name":"family with sequence similarity 157 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34079]","synonyms":"GTF2IP18","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728262","summary":null,"start":198153287,"end":198222513,"strand":1,"description":"family with sequence similarity 157 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34079]"}, {"versioned_ensembl_gene_id":"ENSG00000225987.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"G17,PBX2MHC,HOX12","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32251742,"end":32257192,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000230062.5","gene_symbol":"ANKRD66","gene_name":"ankyrin repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:44669]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287718","summary":null,"start":46746917,"end":46759506,"strand":1,"description":"ankyrin repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:44669]"}, {"versioned_ensembl_gene_id":"ENSG00000256560.1","gene_symbol":"LINC01486","gene_name":"long intergenic non-protein coding RNA 1486 [Source:HGNC Symbol;Acc:HGNC:51137]","synonyms":"TCONS_00021407","biotype":"lincRNA","ncbi_id":"101928138","summary":null,"start":109354083,"end":109359488,"strand":-1,"description":"long intergenic non-protein coding RNA 1486 [Source:HGNC Symbol;Acc:HGNC:51137]"}, {"versioned_ensembl_gene_id":"ENSG00000242386.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"RING7,D6S221E","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32968079,"end":32986577,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000156269.4","gene_symbol":"NAA11","gene_name":"N(alpha)-acetyltransferase 11, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:28125]","synonyms":"hARD2,ARD2,ARD1B","biotype":"protein_coding","ncbi_id":"84779","summary":null,"start":79225694,"end":79326050,"strand":-1,"description":"N(alpha)-acetyltransferase 11, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:28125]"}, {"versioned_ensembl_gene_id":"ENSG00000226987.1","gene_symbol":"AL157938.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131240687,"end":131241724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264150.1","gene_symbol":"AP005136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2568392,"end":2569122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198055.10","gene_symbol":"GRK6","gene_name":"G protein-coupled receptor kinase 6 [Source:HGNC Symbol;Acc:HGNC:4545]","synonyms":"GPRK6","biotype":"protein_coding","ncbi_id":"2870","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":177403204,"end":177442901,"strand":1,"description":"G protein-coupled receptor kinase 6 [Source:HGNC Symbol;Acc:HGNC:4545]"}, {"versioned_ensembl_gene_id":"ENSG00000086061.15","gene_symbol":"DNAJA1","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 [Source:HGNC Symbol;Acc:HGNC:5229]","synonyms":"HSPF4,HSJ2,hdj-2,dj-2,NEDD7","biotype":"protein_coding","ncbi_id":"3301","summary":"This gene encodes a member of the DnaJ family of proteins, which act as heat shock protein 70 cochaperones. Heat shock proteins facilitate protein folding, trafficking, prevention of aggregation, and proteolytic degradation. Members of this family are characterized by a highly conserved N-terminal J domain, a glycine/phenylalanine-rich region, four CxxCxGxG zinc finger repeats, and a C-terminal substrate-binding domain. The J domain mediates the interaction with heat shock protein 70 to recruit substrates and regulate ATP hydrolysis activity. In humans, this gene has been implicated in positive regulation of virus replication through co-option by the influenza A virus. Several pseudogenes of this gene are found on other chromosomes. [provided by RefSeq, Sep 2015]","start":33025211,"end":33039907,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A1 [Source:HGNC Symbol;Acc:HGNC:5229]"}, {"versioned_ensembl_gene_id":"ENSG00000090054.13","gene_symbol":"SPTLC1","gene_name":"serine palmitoyltransferase long chain base subunit 1 [Source:HGNC Symbol;Acc:HGNC:11277]","synonyms":"SPTI,LCB1,HSN1,HSAN1,hLCB1","biotype":"protein_coding","ncbi_id":"10558","summary":"This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013]","start":92031999,"end":92115384,"strand":-1,"description":"serine palmitoyltransferase long chain base subunit 1 [Source:HGNC Symbol;Acc:HGNC:11277]"}, {"versioned_ensembl_gene_id":"ENSG00000268231.1","gene_symbol":"AC008743.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50555370,"end":50557969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250597.5","gene_symbol":"AC093689.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34657606,"end":34669432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096717.11","gene_symbol":"SIRT1","gene_name":"sirtuin 1 [Source:HGNC Symbol;Acc:HGNC:14929]","synonyms":"SIR2L1","biotype":"protein_coding","ncbi_id":"23411","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":67884669,"end":67918390,"strand":1,"description":"sirtuin 1 [Source:HGNC Symbol;Acc:HGNC:14929]"}, {"versioned_ensembl_gene_id":"ENSG00000232258.6","gene_symbol":"TMEM114","gene_name":"transmembrane protein 114 [Source:HGNC Symbol;Acc:HGNC:33227]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283953","summary":"This gene encodes a glycosylated transmembrane protein that plays a role in lens and eye development. Mutations in this gene, including a t(16;22)(p13.3;q11.2) translocation, are associated with congenital and juvenile cataract disorders. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":8537605,"end":8590193,"strand":-1,"description":"transmembrane protein 114 [Source:HGNC Symbol;Acc:HGNC:33227]"}, {"versioned_ensembl_gene_id":"ENSG00000279683.1","gene_symbol":"AC090517.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56795382,"end":56795522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276524.1","gene_symbol":"AC010999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56887107,"end":56888219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253370.2","gene_symbol":"AC027308.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":156458398,"end":156458507,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271810.5","gene_symbol":"AL603832.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112702614,"end":112711433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239983.1","gene_symbol":"AC016687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33968174,"end":33968526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282664.1","gene_symbol":"LINC00552","gene_name":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]","synonyms":null,"biotype":"TEC","ncbi_id":"100130386","summary":null,"start":113749533,"end":113752109,"strand":-1,"description":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]"}, {"versioned_ensembl_gene_id":"ENSG00000171466.9","gene_symbol":"ZNF562","gene_name":"zinc finger protein 562 [Source:HGNC Symbol;Acc:HGNC:25950]","synonyms":"FLJ20079","biotype":"protein_coding","ncbi_id":"54811","summary":null,"start":9641808,"end":9675086,"strand":-1,"description":"zinc finger protein 562 [Source:HGNC Symbol;Acc:HGNC:25950]"}, {"versioned_ensembl_gene_id":"ENSG00000284739.1","gene_symbol":"BX005132.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4963954,"end":4973298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226211.1","gene_symbol":"AL445466.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221133865,"end":221134221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237022.10","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"PSORS1,HLA-JY3,D6S204","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31312208,"end":31315579,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000275202.1","gene_symbol":"AL161421.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48974967,"end":48976867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198836.8","gene_symbol":"OPA1","gene_name":"OPA1, mitochondrial dynamin like GTPase [Source:HGNC Symbol;Acc:HGNC:8140]","synonyms":"NTG,NPG,MGM1,KIAA0567,FLJ12460","biotype":"protein_coding","ncbi_id":"4976","summary":"The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]","start":193593144,"end":193697823,"strand":1,"description":"OPA1, mitochondrial dynamin like GTPase [Source:HGNC Symbol;Acc:HGNC:8140]"}, {"versioned_ensembl_gene_id":"ENSG00000143862.7","gene_symbol":"ARL8A","gene_name":"ADP ribosylation factor like GTPase 8A [Source:HGNC Symbol;Acc:HGNC:25192]","synonyms":"Gie2,FLJ45195,ARL10B","biotype":"protein_coding","ncbi_id":"127829","summary":null,"start":202133404,"end":202144743,"strand":-1,"description":"ADP ribosylation factor like GTPase 8A [Source:HGNC Symbol;Acc:HGNC:25192]"}, {"versioned_ensembl_gene_id":"ENSG00000228005.1","gene_symbol":"AC020743.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50141540,"end":50142823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249581.2","gene_symbol":"CLRN2","gene_name":"clarin 2 [Source:HGNC Symbol;Acc:HGNC:33939]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645104","summary":"This gene belongs to the clarin family of genes. The clarins appear to belong to a large superfamily of small integral membrane glycoproteins with four transmembrane domains. The exact function of this gene is unknown. [provided by RefSeq, Oct 2008]","start":17515165,"end":17527104,"strand":1,"description":"clarin 2 [Source:HGNC Symbol;Acc:HGNC:33939]"}, {"versioned_ensembl_gene_id":"ENSG00000253333.1","gene_symbol":"AC146944.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70495100,"end":70500903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250687.6","gene_symbol":"AC146944.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70462244,"end":70479215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134160.13","gene_symbol":"TRPM1","gene_name":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]","synonyms":"LTRPC1,CSNB1C,MLSN1,LTRPC1,CSNB1C,MLSN1","biotype":"protein_coding","ncbi_id":"4308","summary":"This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":31001061,"end":31161273,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]"}, {"versioned_ensembl_gene_id":"ENSG00000234618.1","gene_symbol":"RPSAP9","gene_name":"ribosomal protein SA pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:31463]","synonyms":"LAMR1P9","biotype":"processed_pseudogene","ncbi_id":"653162","summary":null,"start":76398699,"end":76399586,"strand":1,"description":"ribosomal protein SA pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:31463]"}, {"versioned_ensembl_gene_id":"ENSG00000236389.1","gene_symbol":"AL121970.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134706060,"end":134707349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105722.9","gene_symbol":"ERF","gene_name":"ETS2 repressor factor [Source:HGNC Symbol;Acc:HGNC:3444]","synonyms":"PE2,PE-2","biotype":"protein_coding","ncbi_id":"2077","summary":"ETS2 is a transcription factor and protooncogene involved in development, apoptosis, and the regulation of telomerase. The protein encoded by this gene binds to the ETS2 promoter and is a strong repressor of ETS2 transcription. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":42247572,"end":42255157,"strand":-1,"description":"ETS2 repressor factor [Source:HGNC Symbol;Acc:HGNC:3444]"}, {"versioned_ensembl_gene_id":"ENSG00000248779.1","gene_symbol":"AC093297.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44752949,"end":44765744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176040.13","gene_symbol":"TMPRSS7","gene_name":"transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:HGNC:30846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344805","summary":null,"start":112034843,"end":112081269,"strand":1,"description":"transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:HGNC:30846]"}, {"versioned_ensembl_gene_id":"ENSG00000251629.6","gene_symbol":"LINC02241","gene_name":"long intergenic non-protein coding RNA 2241 [Source:HGNC Symbol;Acc:HGNC:53126]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374676","summary":null,"start":20611840,"end":20937691,"strand":1,"description":"long intergenic non-protein coding RNA 2241 [Source:HGNC Symbol;Acc:HGNC:53126]"}, {"versioned_ensembl_gene_id":"ENSG00000266149.1","gene_symbol":"AP001094.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8360820,"end":8367034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274624.1","gene_symbol":"AC007671.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22104491,"end":22105320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197161.7","gene_symbol":"AC023080.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48345351,"end":48352447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119471.14","gene_symbol":"HSDL2","gene_name":"hydroxysteroid dehydrogenase like 2 [Source:HGNC Symbol;Acc:HGNC:18572]","synonyms":"SDR13C1,C9orf99","biotype":"protein_coding","ncbi_id":"84263","summary":null,"start":112379937,"end":112472410,"strand":1,"description":"hydroxysteroid dehydrogenase like 2 [Source:HGNC Symbol;Acc:HGNC:18572]"}, {"versioned_ensembl_gene_id":"ENSG00000187908.16","gene_symbol":"DMBT1","gene_name":"deleted in malignant brain tumors 1 [Source:HGNC Symbol;Acc:HGNC:2926]","synonyms":"vomeroglandin,SALSA,muclin,hensin,GP340,Gp-340","biotype":"protein_coding","ncbi_id":"1755","summary":"Loss of sequences from human chromosome 10q has been associated with the progression of human cancers. This gene was originally isolated based on its deletion in a medulloblastoma cell line. This gene is expressed with transcripts of 6.0, 7.5, and 8.0 kb in fetal lung and with one transcript of 8.0 kb in adult lung, although the 7.5 kb transcript has not been characterized. The encoded protein precursor is a glycoprotein containing multiple scavenger receptor cysteine-rich (SRCR) domains separated by SRCR-interspersed domains (SID). Transcript variant 2 (8.0 kb) has been shown to bind surfactant protein D independently of carbohydrate recognition. This indicates that DMBT1 may not be a classical tumor suppressor gene, but rather play a role in the interaction of tumor cells and the immune system. [provided by RefSeq, Mar 2016]","start":122560665,"end":122643736,"strand":1,"description":"deleted in malignant brain tumors 1 [Source:HGNC Symbol;Acc:HGNC:2926]"}, {"versioned_ensembl_gene_id":"ENSG00000228638.1","gene_symbol":"FCF1P2","gene_name":"FCF1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060195","summary":null,"start":48290793,"end":48291375,"strand":-1,"description":"FCF1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44614]"}, {"versioned_ensembl_gene_id":"ENSG00000176555.1","gene_symbol":"OR4S1","gene_name":"olfactory receptor family 4 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256148","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48306223,"end":48307152,"strand":1,"description":"olfactory receptor family 4 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14705]"}, {"versioned_ensembl_gene_id":"ENSG00000254926.1","gene_symbol":"AP000445.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58748999,"end":58761053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155966.13","gene_symbol":"AFF2","gene_name":"AF4/FMR2 family member 2 [Source:HGNC Symbol;Acc:HGNC:3776]","synonyms":"FRAXE,FMR2","biotype":"protein_coding","ncbi_id":"2334","summary":"This gene encodes a putative transcriptional activator that is a member of the AF4\\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]","start":148500619,"end":149000663,"strand":1,"description":"AF4/FMR2 family member 2 [Source:HGNC Symbol;Acc:HGNC:3776]"}, {"versioned_ensembl_gene_id":"ENSG00000165185.14","gene_symbol":"KIAA1958","gene_name":"KIAA1958 [Source:HGNC Symbol;Acc:HGNC:23427]","synonyms":"FLJ39294","biotype":"protein_coding","ncbi_id":"158405","summary":null,"start":112486847,"end":112669397,"strand":1,"description":"KIAA1958 [Source:HGNC Symbol;Acc:HGNC:23427]"}, {"versioned_ensembl_gene_id":"ENSG00000168542.14","gene_symbol":"COL3A1","gene_name":"collagen type III alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2201]","synonyms":"EDS4A","biotype":"protein_coding","ncbi_id":"1281","summary":"This gene encodes the pro-alpha1 chains of type III collagen, a fibrillar collagen that is found in extensible connective tissues such as skin, lung, uterus, intestine and the vascular system, frequently in association with type I collagen. Mutations in this gene are associated with Ehlers-Danlos syndrome types IV, and with aortic and arterial aneurysms. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]","start":188974320,"end":189012746,"strand":1,"description":"collagen type III alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2201]"}, {"versioned_ensembl_gene_id":"ENSG00000250116.2","gene_symbol":"AC018682.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46568256,"end":46580238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251434.1","gene_symbol":"AC104071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31350284,"end":31351725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158747.13","gene_symbol":"NBL1","gene_name":"neuroblastoma 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:7650]","synonyms":"NO3,NB,DAND1,DAN,D1S1733E","biotype":"protein_coding","ncbi_id":"4681","summary":"This gene product is the founding member of the evolutionarily conserved CAN (Cerberus and DAN) family of proteins, which contain a domain resembling the CTCK (C-terminal cystine knot-like) motif found in a number of signaling molecules. These proteins are secreted, and act as BMP (bone morphogenetic protein) antagonists by binding to BMPs and preventing them from interacting with their receptors. They may thus play an important role during growth and development. Alternatively spliced transcript variants have been identified for this gene. Read-through transcripts between this locus and the upstream mitochondrial inner membrane organizing system 1 gene (GeneID 440574) have been observed. [provided by RefSeq, May 2013]","start":19640554,"end":19658456,"strand":1,"description":"neuroblastoma 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:7650]"}, {"versioned_ensembl_gene_id":"ENSG00000239516.1","gene_symbol":"FLYWCH1P1","gene_name":"FLYWCH-type zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38033]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130898","summary":null,"start":180827977,"end":180829850,"strand":-1,"description":"FLYWCH-type zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38033]"}, {"versioned_ensembl_gene_id":"ENSG00000175619.3","gene_symbol":"OR4B1","gene_name":"olfactory receptor family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8290]","synonyms":"OST208","biotype":"protein_coding","ncbi_id":"119765","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48216810,"end":48217739,"strand":1,"description":"olfactory receptor family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8290]"}, {"versioned_ensembl_gene_id":"ENSG00000250020.1","gene_symbol":"AC113430.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58198,"end":58915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232310.6","gene_symbol":"AL078590.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134525314,"end":134659836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227723.1","gene_symbol":"AL596188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134636489,"end":134642495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236986.6","gene_symbol":"AL157938.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131132852,"end":131167505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254867.1","gene_symbol":"AP006287.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65983679,"end":65984331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250197.1","gene_symbol":"HMGN1P15","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874441","summary":null,"start":115289036,"end":115289330,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39359]"}, {"versioned_ensembl_gene_id":"ENSG00000231995.2","gene_symbol":"AL590399.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62266319,"end":62266919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169605.5","gene_symbol":"GKN1","gene_name":"gastrokine 1 [Source:HGNC Symbol;Acc:HGNC:23217]","synonyms":"CA11,BRICD1,AMP18","biotype":"protein_coding","ncbi_id":"56287","summary":"The protein encoded by this gene is found to be down-regulated in human gastric cancer tissue as compared to normal gastric mucosa. [provided by RefSeq, Jul 2008]","start":68974573,"end":68980974,"strand":1,"description":"gastrokine 1 [Source:HGNC Symbol;Acc:HGNC:23217]"}, {"versioned_ensembl_gene_id":"ENSG00000233456.1","gene_symbol":"LINC01077","gene_name":"long intergenic non-protein coding RNA 1077 [Source:HGNC Symbol;Acc:HGNC:49120]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107080621","summary":null,"start":48570639,"end":48573317,"strand":-1,"description":"long intergenic non-protein coding RNA 1077 [Source:HGNC Symbol;Acc:HGNC:49120]"}, {"versioned_ensembl_gene_id":"ENSG00000118217.5","gene_symbol":"ATF6","gene_name":"activating transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:791]","synonyms":"ATF6A","biotype":"protein_coding","ncbi_id":"22926","summary":"This gene encodes a transcription factor that activates target genes for the unfolded protein response (UPR) during endoplasmic reticulum (ER) stress. Although it is a transcription factor, this protein is unusual in that it is synthesized as a transmembrane protein that is embedded in the ER. It functions as an ER stress sensor/transducer, and following ER stress-induced proteolysis, it functions as a nuclear transcription factor via a cis-acting ER stress response element (ERSE) that is present in the promoters of genes encoding ER chaperones. This protein has been identified as a survival factor for quiescent but not proliferative squamous carcinoma cells. There have been conflicting reports about the association of polymorphisms in this gene with diabetes in different populations, but another polymorphism has been associated with increased plasma cholesterol levels. This gene is also thought to be a potential therapeutic target for cystic fibrosis. [provided by RefSeq, Aug 2011]","start":161766294,"end":161964070,"strand":1,"description":"activating transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:791]"}, {"versioned_ensembl_gene_id":"ENSG00000236266.1","gene_symbol":"Z98884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7810242,"end":7827342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114942.13","gene_symbol":"EEF1B2","gene_name":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1933","summary":"This gene encodes a translation elongation factor. The protein is a guanine nucleotide exchange factor involved in the transfer of aminoacylated tRNAs to the ribosome. Alternative splicing results in three transcript variants which differ only in the 5' UTR. [provided by RefSeq, Jul 2008]","start":206159585,"end":206162928,"strand":1,"description":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]"}, {"versioned_ensembl_gene_id":"ENSG00000151704.15","gene_symbol":"KCNJ1","gene_name":"potassium voltage-gated channel subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:6255]","synonyms":"ROMK1,Kir1.1","biotype":"protein_coding","ncbi_id":"3758","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":128836315,"end":128867373,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:6255]"}, {"versioned_ensembl_gene_id":"ENSG00000278550.4","gene_symbol":"SLC43A2","gene_name":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]","synonyms":"MGC34680","biotype":"protein_coding","ncbi_id":"124935","summary":"This gene encodes a member of the L-amino acid transporter-3 or SLC43 family of transporters. The encoded protein mediates sodium-, chloride-, and pH-independent transport of L-isomers of neutral amino acids, including leucine, phenylalanine, valine and methionine. This protein may contribute to the transfer of amino acids across the placental membrane to the fetus. [provided by RefSeq, Mar 2016]","start":1569973,"end":1628886,"strand":-1,"description":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]"}, {"versioned_ensembl_gene_id":"ENSG00000232783.5","gene_symbol":"FRG2FP","gene_name":"FSHD region gene 2 family member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:51366]","synonyms":"TCONS_l2_00020053","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100128827","summary":null,"start":198110112,"end":198111878,"strand":1,"description":"FSHD region gene 2 family member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:51366]"}, {"versioned_ensembl_gene_id":"ENSG00000262006.1","gene_symbol":"AC005920.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50909637,"end":50910232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273368.1","gene_symbol":"AC006566.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8154558,"end":8155070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229394.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33193611,"end":33194234,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000218305.3","gene_symbol":"CDC14C","gene_name":"cell division cycle 14C, pseudogene [Source:HGNC Symbol;Acc:HGNC:22427]","synonyms":"MGC26484,CDC14CP,CDC14Bretro,CDC14B2","biotype":"processed_pseudogene","ncbi_id":"168448","summary":"This gene represents a retrogene of cell division cycle 14B (CDC14B), which is located on chromosome 9. The introns in the coding sequence have been processed out relative to the CDC14B locus, but there is an intact open reading frame that is missing only some sequence at the N-terminus, including the nuclear localiztion signal, relative to proteins encoded by the CDC14B gene. There is a difference in the subcellular localization of the protein encoded by this gene, relative to its parental gene product. While the parental gene product displays microtubular localization, GFP chimeras of the protein encoded by this gene localize to the endoplasmic reticulum, indicating a possible new functional role for this gene. [provided by RefSeq, Nov 2017]","start":48919765,"end":48926013,"strand":1,"description":"cell division cycle 14C, pseudogene [Source:HGNC Symbol;Acc:HGNC:22427]"}, {"versioned_ensembl_gene_id":"ENSG00000226889.3","gene_symbol":"AL359541.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161765325,"end":161766227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270378.1","gene_symbol":"AC020891.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51351100,"end":51351192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220267.1","gene_symbol":"ACTBP8","gene_name":"actin, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:141]","synonyms":"ACTBP2","biotype":"processed_pseudogene","ncbi_id":"68","summary":null,"start":88275882,"end":88276989,"strand":-1,"description":"actin, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:141]"}, {"versioned_ensembl_gene_id":"ENSG00000280813.1","gene_symbol":"AC092902.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125800930,"end":125801709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281363.1","gene_symbol":"AF186996.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125756086,"end":125756441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280996.1","gene_symbol":"AF186996.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125747135,"end":125748058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108387.14","gene_symbol":"SEPT4","gene_name":"septin 4 [Source:HGNC Symbol;Acc:HGNC:9165]","synonyms":"ARTS,PNUTL2,MART,hucep-7,hCDCREL-2,H5,CE5B3","biotype":"protein_coding","ncbi_id":"5414","summary":"This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer. [provided by RefSeq, Nov 2010]","start":58520250,"end":58540818,"strand":-1,"description":"septin 4 [Source:HGNC Symbol;Acc:HGNC:9165]"}, {"versioned_ensembl_gene_id":"ENSG00000228173.1","gene_symbol":"AC091770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48660575,"end":48663305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226324.1","gene_symbol":"AL358453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71367054,"end":71367303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185662.9","gene_symbol":"SMIM23","gene_name":"small integral membrane protein 23 [Source:HGNC Symbol;Acc:HGNC:34440]","synonyms":"LOC644994,C5orf50","biotype":"protein_coding","ncbi_id":"644994","summary":null,"start":171782432,"end":171796126,"strand":1,"description":"small integral membrane protein 23 [Source:HGNC Symbol;Acc:HGNC:34440]"}, {"versioned_ensembl_gene_id":"ENSG00000236614.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"ZNF463P,dJ111M5.3","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28888823,"end":28889897,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000182107.6","gene_symbol":"TMEM30B","gene_name":"transmembrane protein 30B [Source:HGNC Symbol;Acc:HGNC:27254]","synonyms":"CDC50B","biotype":"protein_coding","ncbi_id":"161291","summary":null,"start":61277370,"end":61281840,"strand":-1,"description":"transmembrane protein 30B [Source:HGNC Symbol;Acc:HGNC:27254]"}, {"versioned_ensembl_gene_id":"ENSG00000087884.14","gene_symbol":"AAMDC","gene_name":"adipogenesis associated Mth938 domain containing [Source:HGNC Symbol;Acc:HGNC:30205]","synonyms":"PTD015,FLJ21035,CK067,C11orf67","biotype":"protein_coding","ncbi_id":"28971","summary":null,"start":77821109,"end":77918432,"strand":1,"description":"adipogenesis associated Mth938 domain containing [Source:HGNC Symbol;Acc:HGNC:30205]"}, {"versioned_ensembl_gene_id":"ENSG00000206072.12","gene_symbol":"SERPINB11","gene_name":"serpin family B member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14221]","synonyms":"EPIPIN","biotype":"protein_coding","ncbi_id":"89778","summary":null,"start":63647579,"end":63726432,"strand":1,"description":"serpin family B member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14221]"}, {"versioned_ensembl_gene_id":"ENSG00000255115.2","gene_symbol":"AP002812.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77914990,"end":77915275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144827.8","gene_symbol":"ABHD10","gene_name":"abhydrolase domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25656]","synonyms":"FLJ11342","biotype":"protein_coding","ncbi_id":"55347","summary":"This gene encodes a mitochondrially-localized enzyme that acts in liver cells as a hydrolase. The encoded protein removes glucuronide from mycophenolic acid acyl-glucuronide. There is a pseudogene for this gene on chromosome 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":111979010,"end":111993363,"strand":1,"description":"abhydrolase domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25656]"}, {"versioned_ensembl_gene_id":"ENSG00000238032.1","gene_symbol":"AC245047.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48177731,"end":48178023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280025.1","gene_symbol":"AL008638.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27102766,"end":27107019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231405.1","gene_symbol":"AL008638.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27143478,"end":27159878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156427.7","gene_symbol":"FGF18","gene_name":"fibroblast growth factor 18 [Source:HGNC Symbol;Acc:HGNC:3674]","synonyms":"FGF-18,ZFGF5","biotype":"protein_coding","ncbi_id":"8817","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. It has been shown in vitro that this protein is able to induce neurite outgrowth in PC12 cells. Studies of the similar proteins in mouse and chick suggested that this protein is a pleiotropic growth factor that stimulates proliferation in a number of tissues, most notably the liver and small intestine. Knockout studies of the similar gene in mice implied the role of this protein in regulating proliferation and differentiation of midline cerebellar structures. [provided by RefSeq, Jul 2008]","start":171419656,"end":171457623,"strand":1,"description":"fibroblast growth factor 18 [Source:HGNC Symbol;Acc:HGNC:3674]"}, {"versioned_ensembl_gene_id":"ENSG00000140262.17","gene_symbol":"TCF12","gene_name":"transcription factor 12 [Source:HGNC Symbol;Acc:HGNC:11623]","synonyms":"HTF4,HsT17266,HEB,bHLHb20","biotype":"protein_coding","ncbi_id":"6938","summary":"The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the formation of heterodimers with other bHLH E-proteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":56918623,"end":57299281,"strand":1,"description":"transcription factor 12 [Source:HGNC Symbol;Acc:HGNC:11623]"}, {"versioned_ensembl_gene_id":"ENSG00000075618.17","gene_symbol":"FSCN1","gene_name":"fascin actin-bundling protein 1 [Source:HGNC Symbol;Acc:HGNC:11148]","synonyms":"SNL,p55,FLJ38511","biotype":"protein_coding","ncbi_id":"6624","summary":"This gene encodes a member of the fascin family of actin-binding proteins. Fascin proteins organize F-actin into parallel bundles, and are required for the formation of actin-based cellular protrusions. The encoded protein plays a critical role in cell migration, motility, adhesion and cellular interactions. Expression of this gene is known to be regulated by several microRNAs, and overexpression of this gene may play a role in the metastasis of multiple types of cancer by increasing cell motility. Expression of this gene is also a marker for Reed-Sternberg cells in Hodgkin's lymphoma. A pseudogene of this gene is located on the long arm of chromosome 15. [provided by RefSeq, Sep 2011]","start":5592823,"end":5606655,"strand":1,"description":"fascin actin-bundling protein 1 [Source:HGNC Symbol;Acc:HGNC:11148]"}, {"versioned_ensembl_gene_id":"ENSG00000227399.1","gene_symbol":"AL391219.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92006062,"end":92006544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233994.2","gene_symbol":"GDI2P2","gene_name":"GDP dissociation inhibitor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420259","summary":null,"start":72274552,"end":72275159,"strand":1,"description":"GDP dissociation inhibitor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37976]"}, {"versioned_ensembl_gene_id":"ENSG00000271123.1","gene_symbol":"ELOCP5","gene_name":"elongin C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38140]","synonyms":"TCEB1P5","biotype":"processed_pseudogene","ncbi_id":"100288493","summary":null,"start":21631683,"end":21632015,"strand":-1,"description":"elongin C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38140]"}, {"versioned_ensembl_gene_id":"ENSG00000281274.1","gene_symbol":"AL139246.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2493437,"end":2494479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269476.1","gene_symbol":"AC010326.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57876765,"end":57916591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172260.14","gene_symbol":"NEGR1","gene_name":"neuronal growth regulator 1 [Source:HGNC Symbol;Acc:HGNC:17302]","synonyms":"Ntra,MGC46680,KILON,IGLON4","biotype":"protein_coding","ncbi_id":"257194","summary":null,"start":71395940,"end":72282734,"strand":-1,"description":"neuronal growth regulator 1 [Source:HGNC Symbol;Acc:HGNC:17302]"}, {"versioned_ensembl_gene_id":"ENSG00000107614.21","gene_symbol":"TRDMT1","gene_name":"tRNA aspartic acid methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2977]","synonyms":"RNMT1,DNMT2","biotype":"protein_coding","ncbi_id":"1787","summary":"This gene encodes a protein responsible for the methylation of aspartic acid transfer RNA, specifically at the cytosine-38 residue in the anticodon loop. This enzyme also possesses residual DNA-(cytosine-C5) methyltransferase activity. While similar in sequence and structure to DNA cytosine methyltransferases, this gene is distinct and highly conserved in its function among taxa. [provided by RefSeq, Jun 2010]","start":17142254,"end":17202054,"strand":-1,"description":"tRNA aspartic acid methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2977]"}, {"versioned_ensembl_gene_id":"ENSG00000260891.1","gene_symbol":"AC020978.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68212401,"end":68221671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261864.1","gene_symbol":"AC130462.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":68077340,"end":68122271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243187.1","gene_symbol":"CCDC39-AS1","gene_name":"CCDC39 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41089]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874112","summary":null,"start":180680084,"end":180700449,"strand":1,"description":"CCDC39 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41089]"}, {"versioned_ensembl_gene_id":"ENSG00000231527.5","gene_symbol":"CR769775.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61972240,"end":61976380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241473.1","gene_symbol":"AC108734.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180820544,"end":180821612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182810.6","gene_symbol":"DDX28","gene_name":"DEAD-box helicase 28 [Source:HGNC Symbol;Acc:HGNC:17330]","synonyms":"MDDX28,FLJ11282","biotype":"protein_coding","ncbi_id":"55794","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene is intronless. It encodes an RNA-dependent ATPase. The encoded protein is localized in the mitochondria and the nucleus, and can be transported between the mitochondria and the nucleus. [provided by RefSeq, Jul 2008]","start":68021274,"end":68023442,"strand":-1,"description":"DEAD-box helicase 28 [Source:HGNC Symbol;Acc:HGNC:17330]"}, {"versioned_ensembl_gene_id":"ENSG00000282556.1","gene_symbol":"AC068733.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6323554,"end":6324023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231971.5","gene_symbol":"AL078590.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134428240,"end":134520585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204514.9","gene_symbol":"ZNF814","gene_name":"zinc finger protein 814 [Source:HGNC Symbol;Acc:HGNC:33258]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730051","summary":null,"start":57848731,"end":57889074,"strand":-1,"description":"zinc finger protein 814 [Source:HGNC Symbol;Acc:HGNC:33258]"}, {"versioned_ensembl_gene_id":"ENSG00000166415.14","gene_symbol":"WDR72","gene_name":"WD repeat domain 72 [Source:HGNC Symbol;Acc:HGNC:26790]","synonyms":"FLJ38736","biotype":"protein_coding","ncbi_id":"256764","summary":"This gene encodes a protein with eight WD-40 repeats. Mutations in this gene have been associated with amelogenesis imperfecta hypomaturation type 2A3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":53513741,"end":53762878,"strand":-1,"description":"WD repeat domain 72 [Source:HGNC Symbol;Acc:HGNC:26790]"}, {"versioned_ensembl_gene_id":"ENSG00000276845.1","gene_symbol":"CR769775.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61944232,"end":61945136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255522.1","gene_symbol":"SNRPCP5","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49820]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480290","summary":null,"start":3531420,"end":3531608,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49820]"}, {"versioned_ensembl_gene_id":"ENSG00000250067.11","gene_symbol":"YJEFN3","gene_name":"YjeF N-terminal domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24785]","synonyms":"hYjeF_N3-19p13.11,FLJ44968","biotype":"protein_coding","ncbi_id":"374887","summary":null,"start":19528861,"end":19537581,"strand":1,"description":"YjeF N-terminal domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24785]"}, {"versioned_ensembl_gene_id":"ENSG00000136630.12","gene_symbol":"HLX","gene_name":"H2.0 like homeobox [Source:HGNC Symbol;Acc:HGNC:4978]","synonyms":"HLX1,HB24","biotype":"protein_coding","ncbi_id":"3142","summary":null,"start":220879400,"end":220885059,"strand":1,"description":"H2.0 like homeobox [Source:HGNC Symbol;Acc:HGNC:4978]"}, {"versioned_ensembl_gene_id":"ENSG00000279848.1","gene_symbol":"AL008638.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27044001,"end":27045315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236858.1","gene_symbol":"AL008638.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27048144,"end":27060518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238195.1","gene_symbol":"AL021153.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27204211,"end":27205126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151475.5","gene_symbol":"SLC25A31","gene_name":"solute carrier family 25 member 31 [Source:HGNC Symbol;Acc:HGNC:25319]","synonyms":"DKFZP434N1235,ANT4","biotype":"protein_coding","ncbi_id":"83447","summary":"The protein encoded by this gene is a member of the ADP/ATP carrier family of proteins that exchange cytosolic ADP for matrix ATP in the mitochondria. Cells over-expressing this gene have been shown to display an anti-apoptotic phenotype. This protein is also thought to play a role in spermatogenesis, where it is believed to associate with a part of the flagellar cytoskeleton and with glycolytic enzymes. Male mice with mutations in the mouse ortholog of this gene are sterile and spermatocytes display an early meiotic arrest phenotype. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":127730378,"end":127774299,"strand":1,"description":"solute carrier family 25 member 31 [Source:HGNC Symbol;Acc:HGNC:25319]"}, {"versioned_ensembl_gene_id":"ENSG00000284674.1","gene_symbol":"BX005132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4973381,"end":4981568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234754.1","gene_symbol":"C1orf140","gene_name":"uncharacterized LOC400804 [Source:NCBI gene;Acc:400804]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400804","summary":null,"start":221330080,"end":221336296,"strand":-1,"description":"uncharacterized LOC400804 [Source:NCBI gene;Acc:400804]"}, {"versioned_ensembl_gene_id":"ENSG00000267656.1","gene_symbol":"AP001357.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13139780,"end":13140489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198729.4","gene_symbol":"PPP1R14C","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14C [Source:HGNC Symbol;Acc:HGNC:14952]","synonyms":"NY-BR-81,KEPI,CPI17-like","biotype":"protein_coding","ncbi_id":"81706","summary":"The degree of protein phosphorylation is regulated by a balance of protein kinase and phosphatase activities. Protein phosphatase-1 (PP1; see MIM 176875) is a signal-transducing phosphatase that influences neuronal activity, protein synthesis, metabolism, muscle contraction, and cell division. PPP1R14C is an inhibitor of PP1 (Liu et al., 2002 [PubMed 11812771]).[supplied by OMIM, Feb 2010]","start":150143076,"end":150250357,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14C [Source:HGNC Symbol;Acc:HGNC:14952]"}, {"versioned_ensembl_gene_id":"ENSG00000231510.1","gene_symbol":"AL691497.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5086459,"end":5090899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231197.1","gene_symbol":"BX927141.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878153,"end":29879115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111863.12","gene_symbol":"ADTRP","gene_name":"androgen dependent TFPI regulating protein [Source:HGNC Symbol;Acc:HGNC:21214]","synonyms":"dJ413H6.1,C6orf105,AIG1L","biotype":"protein_coding","ncbi_id":"84830","summary":null,"start":11712054,"end":11807046,"strand":-1,"description":"androgen dependent TFPI regulating protein [Source:HGNC Symbol;Acc:HGNC:21214]"}, {"versioned_ensembl_gene_id":"ENSG00000232436.1","gene_symbol":"AL360013.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221508559,"end":221510979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227585.2","gene_symbol":"AL360013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221549786,"end":221550643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267032.1","gene_symbol":"AP001357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13151637,"end":13152689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235498.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29848896,"end":29849024,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000284616.1","gene_symbol":"AL139823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5301928,"end":5307394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253550.1","gene_symbol":"AC016065.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6473845,"end":6474288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267286.1","gene_symbol":"AP001198.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13183402,"end":13185617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143507.17","gene_symbol":"DUSP10","gene_name":"dual specificity phosphatase 10 [Source:HGNC Symbol;Acc:HGNC:3065]","synonyms":"MKP5,MKP-5","biotype":"protein_coding","ncbi_id":"11221","summary":"Dual specificity protein phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the MAP kinase superfamily, which is associated with cellular proliferation and differentiation. Different members of this family of dual specificity phosphatases show distinct substrate specificities for MAP kinases, different tissue distribution and subcellular localization, and different modes of expression induction by extracellular stimuli. This gene product binds to and inactivates p38 and SAPK/JNK. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":221701424,"end":221742176,"strand":-1,"description":"dual specificity phosphatase 10 [Source:HGNC Symbol;Acc:HGNC:3065]"}, {"versioned_ensembl_gene_id":"ENSG00000271743.1","gene_symbol":"AF287957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6615604,"end":6617198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224801.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824278,"end":29825257,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000233418.8","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DDX16,PRPF2,DBP2,Prp2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30643349,"end":30663298,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000224375.1","gene_symbol":"AC009276.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134684144,"end":134687990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109956.12","gene_symbol":"B3GAT1","gene_name":"beta-1,3-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:921]","synonyms":"LEU7,HNK-1,GlcAT-P,CD57,NK-1","biotype":"protein_coding","ncbi_id":"27087","summary":"The protein encoded by this gene is a member of the glucuronyltransferase gene family. These enzymes exhibit strict acceptor specificity, recognizing nonreducing terminal sugars and their anomeric linkages. This gene product functions as the key enzyme in a glucuronyl transfer reaction during the biosynthesis of the carbohydrate epitope HNK-1 (human natural killer-1, also known as CD57 and LEU7). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":134378504,"end":134411918,"strand":-1,"description":"beta-1,3-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:921]"}, {"versioned_ensembl_gene_id":"ENSG00000237161.4","gene_symbol":"AC068446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21293653,"end":21295201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230101.5","gene_symbol":"TUBB3P2","gene_name":"tubulin beta 3 class III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42181]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130187","summary":null,"start":134734898,"end":134735129,"strand":-1,"description":"tubulin beta 3 class III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42181]"}, {"versioned_ensembl_gene_id":"ENSG00000108587.15","gene_symbol":"GOSR1","gene_name":"golgi SNAP receptor complex member 1 [Source:HGNC Symbol;Acc:HGNC:4430]","synonyms":"GOLIM2,P28,GS28,GOS28,GOS-28","biotype":"protein_coding","ncbi_id":"9527","summary":"This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30477362,"end":30527592,"strand":1,"description":"golgi SNAP receptor complex member 1 [Source:HGNC Symbol;Acc:HGNC:4430]"}, {"versioned_ensembl_gene_id":"ENSG00000233471.2","gene_symbol":"KRT18P62","gene_name":"keratin 18 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287635","summary":null,"start":19257520,"end":19258806,"strand":1,"description":"keratin 18 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48889]"}, {"versioned_ensembl_gene_id":"ENSG00000164048.13","gene_symbol":"ZNF589","gene_name":"zinc finger protein 589 [Source:HGNC Symbol;Acc:HGNC:16747]","synonyms":"SZF1","biotype":"protein_coding","ncbi_id":"51385","summary":null,"start":48241100,"end":48299253,"strand":1,"description":"zinc finger protein 589 [Source:HGNC Symbol;Acc:HGNC:16747]"}, {"versioned_ensembl_gene_id":"ENSG00000235116.1","gene_symbol":"BX649210.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32624375,"end":32624782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196610.13","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32684806,"end":32692245,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000103495.13","gene_symbol":"MAZ","gene_name":"MYC associated zinc finger protein [Source:HGNC Symbol;Acc:HGNC:6914]","synonyms":"ZNF801,Zif87,ZF87,Pur-1","biotype":"protein_coding","ncbi_id":"4150","summary":null,"start":29806106,"end":29811164,"strand":1,"description":"MYC associated zinc finger protein [Source:HGNC Symbol;Acc:HGNC:6914]"}, {"versioned_ensembl_gene_id":"ENSG00000278153.1","gene_symbol":"AL121782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13368291,"end":13368703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267677.1","gene_symbol":"AC016229.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59360700,"end":59386749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236989.5","gene_symbol":"AC130710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16085222,"end":16105841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229662.2","gene_symbol":"AC245047.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48244894,"end":48245745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168484.12","gene_symbol":"SFTPC","gene_name":"surfactant protein C [Source:HGNC Symbol;Acc:HGNC:10802]","synonyms":"SP-C,SMDP2,SFTP2,PSP-C,BRICD6","biotype":"protein_coding","ncbi_id":"6440","summary":"This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.[provided by RefSeq, Feb 2010]","start":22156913,"end":22164479,"strand":1,"description":"surfactant protein C [Source:HGNC Symbol;Acc:HGNC:10802]"}, {"versioned_ensembl_gene_id":"ENSG00000226764.2","gene_symbol":"AC010145.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15997049,"end":16062885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241207.1","gene_symbol":"AC245047.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48276704,"end":48277578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227105.1","gene_symbol":"PARP1P1","gene_name":"poly(ADP-ribose) polymerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:275]","synonyms":"PPOLP1,ADPRTP1","biotype":"processed_pseudogene","ncbi_id":"144","summary":null,"start":110936759,"end":110939784,"strand":1,"description":"poly(ADP-ribose) polymerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:275]"}, {"versioned_ensembl_gene_id":"ENSG00000275582.1","gene_symbol":"AL031670.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3921279,"end":3923400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236289.2","gene_symbol":"GACAT3","gene_name":"gastric cancer associated transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50847]","synonyms":"lncRNA-AC130710,LINC01458","biotype":"lincRNA","ncbi_id":"104797537","summary":null,"start":16050427,"end":16085801,"strand":1,"description":"gastric cancer associated transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50847]"}, {"versioned_ensembl_gene_id":"ENSG00000224087.1","gene_symbol":"AC018865.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130107684,"end":130109741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126752.7","gene_symbol":"SSX1","gene_name":"SSX family member 1 [Source:HGNC Symbol;Acc:HGNC:11335]","synonyms":"CT5.1","biotype":"protein_coding","ncbi_id":"6756","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX2 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Jul 2013]","start":48255317,"end":48267444,"strand":1,"description":"SSX family member 1 [Source:HGNC Symbol;Acc:HGNC:11335]"}, {"versioned_ensembl_gene_id":"ENSG00000228471.1","gene_symbol":"AC018865.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130082092,"end":130082220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196604.12","gene_symbol":"POTEF","gene_name":"POTE ankyrin domain family member F [Source:HGNC Symbol;Acc:HGNC:33905]","synonyms":"POTEACTIN,POTE2alpha,A26C1B","biotype":"protein_coding","ncbi_id":"728378","summary":null,"start":130074030,"end":130129222,"strand":-1,"description":"POTE ankyrin domain family member F [Source:HGNC Symbol;Acc:HGNC:33905]"}, {"versioned_ensembl_gene_id":"ENSG00000160224.16","gene_symbol":"AIRE","gene_name":"autoimmune regulator [Source:HGNC Symbol;Acc:HGNC:360]","synonyms":"PGA1,APS1,APECED","biotype":"protein_coding","ncbi_id":"326","summary":"This gene encodes a transcriptional regulator that forms nuclear bodies and interacts with the transcriptional coactivator CREB binding protein. The encoded protein plays an important role in immunity by regulating the expression of autoantigens and negative selection of autoreactive T-cells in the thymus. Mutations in this gene cause the rare autosomal-recessive systemic autoimmune disease termed autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED). [provided by RefSeq, Jun 2012]","start":44285838,"end":44298648,"strand":1,"description":"autoimmune regulator [Source:HGNC Symbol;Acc:HGNC:360]"}, {"versioned_ensembl_gene_id":"ENSG00000125779.21","gene_symbol":"PANK2","gene_name":"pantothenate kinase 2 [Source:HGNC Symbol;Acc:HGNC:15894]","synonyms":"PKAN,NBIA1,HSS,HARP,FLJ11729,C20orf48","biotype":"protein_coding","ncbi_id":"80025","summary":"This gene encodes a protein belonging to the pantothenate kinase family and is the only member of that family to be expressed in mitochondria. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by acyl CoA species. Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. Alternative splicing, involving the use of alternate first exons, results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]","start":3888839,"end":3929882,"strand":1,"description":"pantothenate kinase 2 [Source:HGNC Symbol;Acc:HGNC:15894]"}, {"versioned_ensembl_gene_id":"ENSG00000264080.1","gene_symbol":"AP005057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1780329,"end":1782064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266602.1","gene_symbol":"AC008109.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1509183,"end":1647097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258674.5","gene_symbol":"AC011448.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":19516227,"end":19536076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183230.16","gene_symbol":"CTNNA3","gene_name":"catenin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2511]","synonyms":"VR22,MGC26194","biotype":"protein_coding","ncbi_id":"29119","summary":"This gene encodes a protein that belongs to the vinculin/alpha-catenin family. The encoded protein plays a role in cell-cell adhesion in muscle cells. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":65912518,"end":67696169,"strand":-1,"description":"catenin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2511]"}, {"versioned_ensembl_gene_id":"ENSG00000070371.15","gene_symbol":"CLTCL1","gene_name":"clathrin heavy chain like 1 [Source:HGNC Symbol;Acc:HGNC:2093]","synonyms":"CLTD,CLTCL,CLH22,CHC22","biotype":"protein_coding","ncbi_id":"8218","summary":"This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":19179473,"end":19291716,"strand":-1,"description":"clathrin heavy chain like 1 [Source:HGNC Symbol;Acc:HGNC:2093]"}, {"versioned_ensembl_gene_id":"ENSG00000230370.1","gene_symbol":"RPL23AP52","gene_name":"ribosomal protein L23a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36723]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271465","summary":null,"start":11006399,"end":11006876,"strand":-1,"description":"ribosomal protein L23a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36723]"}, {"versioned_ensembl_gene_id":"ENSG00000106443.15","gene_symbol":"PHF14","gene_name":"PHD finger protein 14 [Source:HGNC Symbol;Acc:HGNC:22203]","synonyms":"KIAA0783","biotype":"protein_coding","ncbi_id":"9678","summary":null,"start":10973872,"end":11169630,"strand":1,"description":"PHD finger protein 14 [Source:HGNC Symbol;Acc:HGNC:22203]"}, {"versioned_ensembl_gene_id":"ENSG00000227925.1","gene_symbol":"LINC01655","gene_name":"long intergenic non-protein coding RNA 1655 [Source:HGNC Symbol;Acc:HGNC:52443]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929771","summary":null,"start":221827666,"end":221840666,"strand":-1,"description":"long intergenic non-protein coding RNA 1655 [Source:HGNC Symbol;Acc:HGNC:52443]"}, {"versioned_ensembl_gene_id":"ENSG00000266450.1","gene_symbol":"AC019183.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1655177,"end":1779955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204648.11","gene_symbol":"SSX9","gene_name":"SSX family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:19655]","synonyms":"SSX9P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"280660","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene appears not to be involved in this type of chromosome translocation. [provided by RefSeq, Jul 2008]","start":48296816,"end":48306179,"strand":-1,"description":"SSX family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:19655]"}, {"versioned_ensembl_gene_id":"ENSG00000238042.5","gene_symbol":"LINC02257","gene_name":"long intergenic non-protein coding RNA 2257 [Source:HGNC Symbol;Acc:HGNC:53159]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221880981,"end":221978523,"strand":-1,"description":"long intergenic non-protein coding RNA 2257 [Source:HGNC Symbol;Acc:HGNC:53159]"}, {"versioned_ensembl_gene_id":"ENSG00000204368.6","gene_symbol":"AC245047.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48212791,"end":48218010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228437.5","gene_symbol":"LINC02474","gene_name":"long intergenic non-protein coding RNA 2474 [Source:HGNC Symbol;Acc:HGNC:53417]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221966341,"end":221984964,"strand":1,"description":"long intergenic non-protein coding RNA 2474 [Source:HGNC Symbol;Acc:HGNC:53417]"}, {"versioned_ensembl_gene_id":"ENSG00000197566.9","gene_symbol":"ZNF624","gene_name":"zinc finger protein 624 [Source:HGNC Symbol;Acc:HGNC:29254]","synonyms":"KIAA1349","biotype":"protein_coding","ncbi_id":"57547","summary":null,"start":16620737,"end":16653856,"strand":-1,"description":"zinc finger protein 624 [Source:HGNC Symbol;Acc:HGNC:29254]"}, {"versioned_ensembl_gene_id":"ENSG00000237345.1","gene_symbol":"AC245047.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48279423,"end":48281792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225981.1","gene_symbol":"AC102953.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1459937,"end":1464008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232813.1","gene_symbol":"AC245047.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48274904,"end":48275047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234780.1","gene_symbol":"AC245047.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48197221,"end":48199431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231568.1","gene_symbol":"AC245047.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48228833,"end":48228959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165583.14","gene_symbol":"SSX5","gene_name":"SSX family member 5 [Source:HGNC Symbol;Acc:HGNC:11339]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6758","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. While some of the related SSX genes are involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas, this gene does not appear to be involved in such translocations. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2013]","start":48186220,"end":48196763,"strand":-1,"description":"SSX family member 5 [Source:HGNC Symbol;Acc:HGNC:11339]"}, {"versioned_ensembl_gene_id":"ENSG00000225513.1","gene_symbol":"AL158824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112173522,"end":112173971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144834.13","gene_symbol":"TAGLN3","gene_name":"transgelin 3 [Source:HGNC Symbol;Acc:HGNC:29868]","synonyms":"NP25,NP22","biotype":"protein_coding","ncbi_id":"29114","summary":null,"start":111998664,"end":112013887,"strand":1,"description":"transgelin 3 [Source:HGNC Symbol;Acc:HGNC:29868]"}, {"versioned_ensembl_gene_id":"ENSG00000251132.1","gene_symbol":"AC094104.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115031273,"end":115031894,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250242.1","gene_symbol":"AC094104.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115087892,"end":115088475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114446.4","gene_symbol":"IFT57","gene_name":"intraflagellar transport 57 [Source:HGNC Symbol;Acc:HGNC:17367]","synonyms":"FLJ10147,ESRRBL1,MHS4R2,HIPPI","biotype":"protein_coding","ncbi_id":"55081","summary":null,"start":108160812,"end":108222570,"strand":-1,"description":"intraflagellar transport 57 [Source:HGNC Symbol;Acc:HGNC:17367]"}, {"versioned_ensembl_gene_id":"ENSG00000108641.14","gene_symbol":"B9D1","gene_name":"B9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24123]","synonyms":"MKS9,EPPB9,B9","biotype":"protein_coding","ncbi_id":"27077","summary":"This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]","start":19337554,"end":19378182,"strand":-1,"description":"B9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24123]"}, {"versioned_ensembl_gene_id":"ENSG00000198739.10","gene_symbol":"LRRTM3","gene_name":"leucine rich repeat transmembrane neuronal 3 [Source:HGNC Symbol;Acc:HGNC:19410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347731","summary":null,"start":66926006,"end":67099830,"strand":1,"description":"leucine rich repeat transmembrane neuronal 3 [Source:HGNC Symbol;Acc:HGNC:19410]"}, {"versioned_ensembl_gene_id":"ENSG00000108821.13","gene_symbol":"COL1A1","gene_name":"collagen type I alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2197]","synonyms":"OI4","biotype":"protein_coding","ncbi_id":"1277","summary":"This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]","start":50183289,"end":50201632,"strand":-1,"description":"collagen type I alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2197]"}, {"versioned_ensembl_gene_id":"ENSG00000112494.9","gene_symbol":"UNC93A","gene_name":"unc-93 homolog A (C. elegans) [Source:HGNC Symbol;Acc:HGNC:12570]","synonyms":"dJ366N23.2,dJ366N23.1","biotype":"protein_coding","ncbi_id":"54346","summary":null,"start":167271169,"end":167316019,"strand":1,"description":"unc-93 homolog A (C. elegans) [Source:HGNC Symbol;Acc:HGNC:12570]"}, {"versioned_ensembl_gene_id":"ENSG00000248693.1","gene_symbol":"LINC02100","gene_name":"long intergenic non-protein coding RNA 2100 [Source:HGNC Symbol;Acc:HGNC:52955]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986408","summary":null,"start":18704433,"end":18746173,"strand":-1,"description":"long intergenic non-protein coding RNA 2100 [Source:HGNC Symbol;Acc:HGNC:52955]"}, {"versioned_ensembl_gene_id":"ENSG00000249191.1","gene_symbol":"UBE2V1P12","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479048","summary":null,"start":18886622,"end":18887095,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44897]"}, {"versioned_ensembl_gene_id":"ENSG00000249927.1","gene_symbol":"AC025768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18893902,"end":18894168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148516.21","gene_symbol":"ZEB1","gene_name":"zinc finger E-box binding homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11642]","synonyms":"Zfhx1a,Zfhep,ZEB,TCF8,PPCD3,NIL-2-A,FECD6,BZP,AREB6","biotype":"protein_coding","ncbi_id":"6935","summary":"This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010]","start":31318495,"end":31529814,"strand":1,"description":"zinc finger E-box binding homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11642]"}, {"versioned_ensembl_gene_id":"ENSG00000132294.14","gene_symbol":"EFR3A","gene_name":"EFR3 homolog A [Source:HGNC Symbol;Acc:HGNC:28970]","synonyms":"KIAA0143","biotype":"protein_coding","ncbi_id":"23167","summary":"The protein encoded by this gene is part of a complex that plays a role in maintaining an active pool of phosphatidylinositol 4-kinase (PI4K) at the plasma membrane. This protein is thought to be a peripheral membrane protein that associates with the plasma membrane through palmitoylation. Studies indicate that this gene product plays a role in controlling G protein-coupled receptor (GPCR) activity by affecting receptor phosphorylation. Whole exome sequencing studies have implicated mutations in this gene with autism spectrum disorders. [provided by RefSeq, Apr 2016]","start":131904088,"end":132013642,"strand":1,"description":"EFR3 homolog A [Source:HGNC Symbol;Acc:HGNC:28970]"}, {"versioned_ensembl_gene_id":"ENSG00000135334.8","gene_symbol":"AKIRIN2","gene_name":"akirin 2 [Source:HGNC Symbol;Acc:HGNC:21407]","synonyms":"FLJ10342,dJ486L4.2,C6orf166","biotype":"protein_coding","ncbi_id":"55122","summary":null,"start":87675072,"end":87702209,"strand":-1,"description":"akirin 2 [Source:HGNC Symbol;Acc:HGNC:21407]"}, {"versioned_ensembl_gene_id":"ENSG00000172186.7","gene_symbol":"HMGN1P35","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39379]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874448","summary":null,"start":69174124,"end":69174717,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39379]"}, {"versioned_ensembl_gene_id":"ENSG00000236978.1","gene_symbol":"AC073873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70837738,"end":70838013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196235.13","gene_symbol":"SUPT5H","gene_name":"SPT5 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11469]","synonyms":"SPT5H,SPT5,FLJ34157","biotype":"protein_coding","ncbi_id":"6829","summary":null,"start":39436156,"end":39476670,"strand":1,"description":"SPT5 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11469]"}, {"versioned_ensembl_gene_id":"ENSG00000215162.1","gene_symbol":"LINC00269","gene_name":"long intergenic non-protein coding RNA 269 [Source:HGNC Symbol;Acc:HGNC:26586]","synonyms":"NCRNA00269,FLJ33610,CXorf62","biotype":"lincRNA","ncbi_id":"100996279","summary":null,"start":69179557,"end":69209924,"strand":1,"description":"long intergenic non-protein coding RNA 269 [Source:HGNC Symbol;Acc:HGNC:26586]"}, {"versioned_ensembl_gene_id":"ENSG00000160392.13","gene_symbol":"C19orf47","gene_name":"chromosome 19 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26723]","synonyms":"FLJ36888","biotype":"protein_coding","ncbi_id":"126526","summary":null,"start":40319536,"end":40348527,"strand":-1,"description":"chromosome 19 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26723]"}, {"versioned_ensembl_gene_id":"ENSG00000072736.18","gene_symbol":"NFATC3","gene_name":"nuclear factor of activated T-cells 3 [Source:HGNC Symbol;Acc:HGNC:7777]","synonyms":"NFATX,NFAT4","biotype":"protein_coding","ncbi_id":"4775","summary":"The product of this gene is a member of the nuclear factors of activated T cells DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor (TCR) stimulation and an inducible nuclear component. Other members of this family participate to form this complex also. The product of this gene plays a role in the regulation of gene expression in T cells and immature thymocytes. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Nov 2010]","start":68084751,"end":68229259,"strand":1,"description":"nuclear factor of activated T-cells 3 [Source:HGNC Symbol;Acc:HGNC:7777]"}, {"versioned_ensembl_gene_id":"ENSG00000233521.5","gene_symbol":"LINC01638","gene_name":"long intergenic non-protein coding RNA 1638 [Source:HGNC Symbol;Acc:HGNC:52425]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372978","summary":null,"start":27221349,"end":27224727,"strand":-1,"description":"long intergenic non-protein coding RNA 1638 [Source:HGNC Symbol;Acc:HGNC:52425]"}, {"versioned_ensembl_gene_id":"ENSG00000230876.6","gene_symbol":"LINC00486","gene_name":"long intergenic non-protein coding RNA 486 [Source:HGNC Symbol;Acc:HGNC:42946]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285045","summary":null,"start":32825443,"end":32926693,"strand":1,"description":"long intergenic non-protein coding RNA 486 [Source:HGNC Symbol;Acc:HGNC:42946]"}, {"versioned_ensembl_gene_id":"ENSG00000282349.1","gene_symbol":"AC237298.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76515627,"end":76520574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267061.1","gene_symbol":"AC090213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59563709,"end":59568615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233574.1","gene_symbol":"AL020994.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27276240,"end":27286349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276184.4","gene_symbol":"UPK3B","gene_name":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]","synonyms":"UPIIIb,p35,MGC10902,FLJ32198","biotype":"protein_coding","ncbi_id":"105375355","summary":"UPK3B is a minor component of the apical plaques of mammalian urothelium that binds and dimerizes with uroplakin-1b (UPK1B; MIM 602380), one of the major conserved urothelium membrane proteins. The other major conserved integral membrane proteins of urothelial plaques are UPK1A (MIM 611557), UPK2 (MIM 611558), and UPK3A (MIM 611559) (Deng et al., 2002 [PubMed 12446744]).[supplied by OMIM, Mar 2008]","start":76510496,"end":76515744,"strand":1,"description":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]"}, {"versioned_ensembl_gene_id":"ENSG00000267000.1","gene_symbol":"AC016229.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59459072,"end":59465682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223726.1","gene_symbol":"AL020994.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27307483,"end":27318538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267774.2","gene_symbol":"AC010776.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59696459,"end":59698111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226741.1","gene_symbol":"LINC02554","gene_name":"long intergenic non-protein coding RNA 2554 [Source:HGNC Symbol;Acc:HGNC:53594]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507657","summary":null,"start":27310651,"end":27317456,"strand":1,"description":"long intergenic non-protein coding RNA 2554 [Source:HGNC Symbol;Acc:HGNC:53594]"}, {"versioned_ensembl_gene_id":"ENSG00000183287.13","gene_symbol":"CCBE1","gene_name":"collagen and calcium binding EGF domains 1 [Source:HGNC Symbol;Acc:HGNC:29426]","synonyms":"KIAA1983,FLJ30681","biotype":"protein_coding","ncbi_id":"147372","summary":"This gene is thought to function in extracellular matrix remodeling and migration. It is predominantly expressed in the ovary, but down regulated in ovarian cancer cell lines and primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have been associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans. [provided by RefSeq, Mar 2010]","start":59430940,"end":59697380,"strand":-1,"description":"collagen and calcium binding EGF domains 1 [Source:HGNC Symbol;Acc:HGNC:29426]"}, {"versioned_ensembl_gene_id":"ENSG00000249285.1","gene_symbol":"AC114981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18908866,"end":18909543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236854.1","gene_symbol":"AL121656.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32927127,"end":32928405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257342.1","gene_symbol":"AC025165.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57694132,"end":57721510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213246.6","gene_symbol":"SUPT4H1","gene_name":"SPT4 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11467]","synonyms":"Spt4,SUPT4H,Supt4a,SPT4H","biotype":"protein_coding","ncbi_id":"6827","summary":"This gene encodes the small subunit of DRB (5,6-dichloro-1-beta-d-ribofuranosylbenzimidazole) sensitivity-inducing factor (DSIF) complex, which regulates mRNA processing and transcription elongation by RNA polymerase II. The encoded protein is localized to the nucleus and interacts with the large subunit (SUPT5H) to form the DSIF complex. Related pseudogenes have been identified on chromosomes 2 and 12. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2012]","start":58345175,"end":58353093,"strand":-1,"description":"SPT4 homolog, DSIF elongation factor subunit [Source:HGNC Symbol;Acc:HGNC:11467]"}, {"versioned_ensembl_gene_id":"ENSG00000225299.1","gene_symbol":"AL139240.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67052609,"end":67055028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271643.1","gene_symbol":"AC112220.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33795688,"end":33796950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226448.1","gene_symbol":"RPL7AP51","gene_name":"ribosomal protein L7a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271533","summary":null,"start":67334123,"end":67334882,"strand":1,"description":"ribosomal protein L7a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36826]"}, {"versioned_ensembl_gene_id":"ENSG00000239327.1","gene_symbol":"AL163195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20616644,"end":20616991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280364.1","gene_symbol":"AC005858.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126106459,"end":126107047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135506.15","gene_symbol":"OS9","gene_name":"OS9, endoplasmic reticulum lectin [Source:HGNC Symbol;Acc:HGNC:16994]","synonyms":"OS-9,ERLEC2","biotype":"protein_coding","ncbi_id":"10956","summary":"This gene encodes a protein that is highly expressed in osteosarcomas. This protein binds to the hypoxia-inducible factor 1 (HIF-1), a key regulator of the hypoxic response and angiogenesis, and promotes the degradation of one of its subunits. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":57693955,"end":57721557,"strand":1,"description":"OS9, endoplasmic reticulum lectin [Source:HGNC Symbol;Acc:HGNC:16994]"}, {"versioned_ensembl_gene_id":"ENSG00000271020.1","gene_symbol":"AC112220.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33797149,"end":33797681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277056.1","gene_symbol":"AL607023.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66837457,"end":66837704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273360.1","gene_symbol":"AC022017.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66079243,"end":66118326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115944.14","gene_symbol":"COX7A2L","gene_name":"cytochrome c oxidase subunit 7A2 like [Source:HGNC Symbol;Acc:HGNC:2289]","synonyms":"SIG81,EB1,COX7RP,COX7AR","biotype":"protein_coding","ncbi_id":"9167","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein similar to polypeptides 1 and 2 of subunit VIIa in the C-terminal region, and also highly similar to the mouse Sig81 protein sequence. This gene is expressed in all tissues, and upregulated in a breast cancer cell line after estrogen treatment. It is possible that this gene represents a regulatory subunit of COX and mediates the higher level of energy production in target cells by estrogen. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]","start":42333546,"end":42425088,"strand":-1,"description":"cytochrome c oxidase subunit 7A2 like [Source:HGNC Symbol;Acc:HGNC:2289]"}, {"versioned_ensembl_gene_id":"ENSG00000232832.1","gene_symbol":"LMLN-AS1","gene_name":"LMLN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40738]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873947","summary":null,"start":198038321,"end":198039234,"strand":-1,"description":"LMLN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40738]"}, {"versioned_ensembl_gene_id":"ENSG00000223760.4","gene_symbol":"MED15P9","gene_name":"mediator complex subunit 15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44130]","synonyms":"MED15P2,CCDC74B-AS1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285103","summary":null,"start":130129621,"end":130139417,"strand":1,"description":"mediator complex subunit 15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44130]"}, {"versioned_ensembl_gene_id":"ENSG00000237012.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30637275,"end":30643339,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000185621.11","gene_symbol":"LMLN","gene_name":"leishmanolysin like peptidase [Source:HGNC Symbol;Acc:HGNC:15991]","synonyms":"Msp,Gp63","biotype":"protein_coding","ncbi_id":"89782","summary":"This gene encodes a zinc-metallopeptidase. The encoded protein may play a role in cell migration and invasion. Studies of a similar protein in Drosophila indicate a potential role in mitotic progression. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":197960200,"end":198043720,"strand":1,"description":"leishmanolysin like peptidase [Source:HGNC Symbol;Acc:HGNC:15991]"}, {"versioned_ensembl_gene_id":"ENSG00000274468.1","gene_symbol":"AL512638.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":115479428,"end":115481572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267269.1","gene_symbol":"AC010776.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59685820,"end":59688400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111907.20","gene_symbol":"TPD52L1","gene_name":"tumor protein D52 like 1 [Source:HGNC Symbol;Acc:HGNC:12006]","synonyms":"hD53,D53","biotype":"protein_coding","ncbi_id":"7164","summary":"This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers. The encoded protein is involved in cell proliferation and calcium signaling. It also interacts with the mitogen-activated protein kinase kinase kinase 5 (MAP3K5/ASK1) and positively regulates MAP3K5-induced apoptosis. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2016]","start":125119049,"end":125264407,"strand":1,"description":"tumor protein D52 like 1 [Source:HGNC Symbol;Acc:HGNC:12006]"}, {"versioned_ensembl_gene_id":"ENSG00000231706.2","gene_symbol":"CYCSP43","gene_name":"cytochrome c, somatic pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:24417]","synonyms":"HCP43","biotype":"processed_pseudogene","ncbi_id":"360187","summary":null,"start":69485343,"end":69485652,"strand":-1,"description":"cytochrome c, somatic pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:24417]"}, {"versioned_ensembl_gene_id":"ENSG00000152076.18","gene_symbol":"CCDC74B","gene_name":"coiled-coil domain containing 74B [Source:HGNC Symbol;Acc:HGNC:25267]","synonyms":"DKFZp434E2321","biotype":"protein_coding","ncbi_id":"91409","summary":null,"start":130139287,"end":130145134,"strand":-1,"description":"coiled-coil domain containing 74B [Source:HGNC Symbol;Acc:HGNC:25267]"}, {"versioned_ensembl_gene_id":"ENSG00000108375.12","gene_symbol":"RNF43","gene_name":"ring finger protein 43 [Source:HGNC Symbol;Acc:HGNC:18505]","synonyms":"URCC,FLJ20315,DKFZp781H0392","biotype":"protein_coding","ncbi_id":"54894","summary":"The protein encoded by this gene is a RING-type E3 ubiquitin ligase and is predicted to contain a transmembrane domain, a protease-associated domain, an ectodomain, and a cytoplasmic RING domain. This protein is thought to negatively regulate Wnt signaling, and expression of this gene results in an increase in ubiquitination of frizzled receptors, an alteration in their subcellular distribution, resulting in reduced surface levels of these receptors. Mutations in this gene have been reported in multiple tumor cells, including colorectal and endometrial cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]","start":58352500,"end":58417595,"strand":-1,"description":"ring finger protein 43 [Source:HGNC Symbol;Acc:HGNC:18505]"}, {"versioned_ensembl_gene_id":"ENSG00000130054.4","gene_symbol":"FAM155B","gene_name":"family with sequence similarity 155 member B [Source:HGNC Symbol;Acc:HGNC:30701]","synonyms":"TMEM28,TED,CXorf63","biotype":"protein_coding","ncbi_id":"27112","summary":"This gene encodes a product belonging to a family of proteins with unknown function. The presence of two transmembrane domains suggests that this protein is a multi-pass membrane protein. [provided by RefSeq, Sep 2011]","start":69505241,"end":69532508,"strand":1,"description":"family with sequence similarity 155 member B [Source:HGNC Symbol;Acc:HGNC:30701]"}, {"versioned_ensembl_gene_id":"ENSG00000116138.12","gene_symbol":"DNAJC16","gene_name":"DnaJ heat shock protein family (Hsp40) member C16 [Source:HGNC Symbol;Acc:HGNC:29157]","synonyms":"KIAA0962","biotype":"protein_coding","ncbi_id":"23341","summary":null,"start":15526813,"end":15592379,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C16 [Source:HGNC Symbol;Acc:HGNC:29157]"}, {"versioned_ensembl_gene_id":"ENSG00000247765.2","gene_symbol":"AC068446.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21298233,"end":21325241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275839.1","gene_symbol":"AC243654.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37454171,"end":37454931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273965.1","gene_symbol":"AC243654.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37407936,"end":37408594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280703.1","gene_symbol":"AC060814.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21342171,"end":21343958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160396.8","gene_symbol":"HIPK4","gene_name":"homeodomain interacting protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:19007]","synonyms":"FLJ32818","biotype":"protein_coding","ncbi_id":"147746","summary":"This gene encodes a member of the homeodomain interacting protein kinase (HIPK) family of proteins. While other members of this family are found throughout vertebrates, this member is present only in mammals. Compared to other members of this family, the encoded protein lacks a nuclear localization signal and a C-terminal autoinhibitory domain. The encoded protein exhibits kinase activity and may phosphorylate the tumor suppressor protein p53. [provided by RefSeq, Jul 2016]","start":40379271,"end":40390187,"strand":-1,"description":"homeodomain interacting protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:19007]"}, {"versioned_ensembl_gene_id":"ENSG00000280881.1","gene_symbol":"AC060814.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21328380,"end":21343881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236608.1","gene_symbol":"EIF4A1P6","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390407","summary":null,"start":60636888,"end":60638097,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37925]"}, {"versioned_ensembl_gene_id":"ENSG00000276234.4","gene_symbol":"TADA2A","gene_name":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]","synonyms":"hADA2,ADA2A,ADA2,TADA2L","biotype":"protein_coding","ncbi_id":"6871","summary":"Many DNA-binding transcriptional activator proteins enhance the initiation rate of RNA polymerase II-mediated gene transcription by interacting functionally with the general transcription machinery bound at the basal promoter. Adaptor proteins are usually required for this activation, possibly to acetylate and destabilize nucleosomes, thereby relieving chromatin constraints at the promoter. The protein encoded by this gene is a transcriptional activator adaptor and has been found to be part of the PCAF histone acetylase complex. Several alternatively spliced transcript variants encoding different isoforms of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2009]","start":37406874,"end":37479730,"strand":1,"description":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]"}, {"versioned_ensembl_gene_id":"ENSG00000258415.2","gene_symbol":"AC060814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21344548,"end":21345085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239780.1","gene_symbol":"AC090638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50457887,"end":50458795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235049.1","gene_symbol":"LINC00940","gene_name":"long intergenic non-protein coding RNA 940 [Source:HGNC Symbol;Acc:HGNC:48634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100271702","summary":null,"start":1929202,"end":1936574,"strand":-1,"description":"long intergenic non-protein coding RNA 940 [Source:HGNC Symbol;Acc:HGNC:48634]"}, {"versioned_ensembl_gene_id":"ENSG00000180113.15","gene_symbol":"TDRD6","gene_name":"tudor domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21339]","synonyms":"SPATA36,NY-CO-45,CT41.2,bA446F17.4","biotype":"protein_coding","ncbi_id":"221400","summary":"This gene encodes a tudor domain-containing protein and component of the chromatoid body, a type of ribonucleoprotein granule present in male germ cells. Studies in rodents have demonstrated a role for the encoded protein in spermiogenesis and the nonsense mediated decay (NMD) pathway. This protein is a major autoantigen in human patients with autoimmune polyendocrine syndrome type 1 (APS1). [provided by RefSeq, Oct 2016]","start":46687875,"end":46704319,"strand":1,"description":"tudor domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21339]"}, {"versioned_ensembl_gene_id":"ENSG00000241832.1","gene_symbol":"CECR3","gene_name":"cat eye syndrome chromosome region, candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1841]","synonyms":null,"biotype":"lincRNA","ncbi_id":"27442","summary":null,"start":17256859,"end":17266733,"strand":-1,"description":"cat eye syndrome chromosome region, candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1841]"}, {"versioned_ensembl_gene_id":"ENSG00000280893.1","gene_symbol":"AC009133.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29812261,"end":29820092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279759.1","gene_symbol":"AC118344.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40355842,"end":40360606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157557.11","gene_symbol":"ETS2","gene_name":"ETS proto-oncogene 2, transcription factor [Source:HGNC Symbol;Acc:HGNC:3489]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2114","summary":"This gene encodes a transcription factor which regulates genes involved in development and apoptosis. The encoded protein is also a protooncogene and shown to be involved in regulation of telomerase. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":38805307,"end":38824955,"strand":1,"description":"ETS proto-oncogene 2, transcription factor [Source:HGNC Symbol;Acc:HGNC:3489]"}, {"versioned_ensembl_gene_id":"ENSG00000242973.6","gene_symbol":"AL591242.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46670444,"end":46688165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167371.17","gene_symbol":"PRRT2","gene_name":"proline rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30500]","synonyms":"PKC,IFITMD1,ICCA,FLJ25513,FICCA,EKD1,DYT10,DSPB3,DKFZp547J199","biotype":"protein_coding","ncbi_id":"112476","summary":"This gene encodes a transmembrane protein containing a proline-rich domain in its N-terminal half. Studies in mice suggest that it is predominantly expressed in brain and spinal cord in embryonic and postnatal stages. Mutations in this gene are associated with episodic kinesigenic dyskinesia-1. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":29811382,"end":29815892,"strand":1,"description":"proline rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30500]"}, {"versioned_ensembl_gene_id":"ENSG00000232021.6","gene_symbol":"LEF1-AS1","gene_name":"LEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40339]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"641518","summary":null,"start":108167525,"end":108256836,"strand":1,"description":"LEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40339]"}, {"versioned_ensembl_gene_id":"ENSG00000262788.3","gene_symbol":"UTP4","gene_name":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]","synonyms":"TEX292,NAIC,KIAA1988,FLJ14728,CIRHIN,CIRH1A","biotype":"protein_coding","ncbi_id":"84916","summary":"This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":69142116,"end":69169025,"strand":1,"description":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]"}, {"versioned_ensembl_gene_id":"ENSG00000227567.7","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31634594,"end":31640388,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000104738.16","gene_symbol":"MCM4","gene_name":"minichromosome maintenance complex component 4 [Source:HGNC Symbol;Acc:HGNC:6947]","synonyms":"P1-Cdc21,MGC33310,hCdc21,CDC54,CDC21","biotype":"protein_coding","ncbi_id":"4173","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 6 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of this protein by CDC2 kinase reduces the DNA helicase activity and chromatin binding of the MCM complex. This gene is mapped to a region on the chromosome 8 head-to-head next to the PRKDC/DNA-PK, a DNA-activated protein kinase involved in the repair of DNA double-strand breaks. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":47960185,"end":47978160,"strand":1,"description":"minichromosome maintenance complex component 4 [Source:HGNC Symbol;Acc:HGNC:6947]"}, {"versioned_ensembl_gene_id":"ENSG00000146070.16","gene_symbol":"PLA2G7","gene_name":"phospholipase A2 group VII [Source:HGNC Symbol;Acc:HGNC:9040]","synonyms":"PAFAH,LDL-PLA2","biotype":"protein_coding","ncbi_id":"7941","summary":"The protein encoded by this gene is a secreted enzyme that catalyzes the degradation of platelet-activating factor to biologically inactive products. Defects in this gene are a cause of platelet-activating factor acetylhydrolase deficiency. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2009]","start":46704201,"end":46735693,"strand":-1,"description":"phospholipase A2 group VII [Source:HGNC Symbol;Acc:HGNC:9040]"}, {"versioned_ensembl_gene_id":"ENSG00000148180.19","gene_symbol":"GSN","gene_name":"gelsolin [Source:HGNC Symbol;Acc:HGNC:4620]","synonyms":"DKFZp313L0718","biotype":"protein_coding","ncbi_id":"2934","summary":"The protein encoded by this gene binds to the \"plus\" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":121207794,"end":121332843,"strand":1,"description":"gelsolin [Source:HGNC Symbol;Acc:HGNC:4620]"}, {"versioned_ensembl_gene_id":"ENSG00000099399.5","gene_symbol":"MAGEB2","gene_name":"MAGE family member B2 [Source:HGNC Symbol;Acc:HGNC:6809]","synonyms":"DAM6,CT3.2,MGC26438,MAGE-XP-2","biotype":"protein_coding","ncbi_id":"4113","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region. It is expressed in testis and placenta, and in a significant fraction of tumors of various histological types. The MAGEB genes are clustered on chromosome Xp22-p21. [provided by RefSeq, Jul 2008]","start":30215560,"end":30220089,"strand":1,"description":"MAGE family member B2 [Source:HGNC Symbol;Acc:HGNC:6809]"}, {"versioned_ensembl_gene_id":"ENSG00000256681.1","gene_symbol":"CCDC58P5","gene_name":"coiled-coil domain containing 58 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420588","summary":null,"start":73850469,"end":73851211,"strand":-1,"description":"coiled-coil domain containing 58 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45028]"}, {"versioned_ensembl_gene_id":"ENSG00000281950.1","gene_symbol":"SPDYE16","gene_name":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723555","summary":null,"start":76519194,"end":76529340,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]"}, {"versioned_ensembl_gene_id":"ENSG00000237586.3","gene_symbol":"AC090192.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124301315,"end":124301804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175581.13","gene_symbol":"MRPL48","gene_name":"mitochondrial ribosomal protein L48 [Source:HGNC Symbol;Acc:HGNC:16653]","synonyms":"CGI-118","biotype":"protein_coding","ncbi_id":"51642","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 6p. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]","start":73787316,"end":73865133,"strand":1,"description":"mitochondrial ribosomal protein L48 [Source:HGNC Symbol;Acc:HGNC:16653]"}, {"versioned_ensembl_gene_id":"ENSG00000034533.11","gene_symbol":"ASTE1","gene_name":"asteroid homolog 1 [Source:HGNC Symbol;Acc:HGNC:25021]","synonyms":"HT001","biotype":"protein_coding","ncbi_id":"28990","summary":null,"start":131013875,"end":131027649,"strand":-1,"description":"asteroid homolog 1 [Source:HGNC Symbol;Acc:HGNC:25021]"}, {"versioned_ensembl_gene_id":"ENSG00000138795.9","gene_symbol":"LEF1","gene_name":"lymphoid enhancer binding factor 1 [Source:HGNC Symbol;Acc:HGNC:6551]","synonyms":"TCF7L3,TCF1ALPHA,TCF10","biotype":"protein_coding","ncbi_id":"51176","summary":"This gene encodes a transcription factor belonging to a family of proteins that share homology with the high mobility group protein-1. The protein encoded by this gene can bind to a functionally important site in the T-cell receptor-alpha enhancer, thereby conferring maximal enhancer activity. This transcription factor is involved in the Wnt signaling pathway, and it may function in hair cell differentiation and follicle morphogenesis. Mutations in this gene have been found in somatic sebaceous tumors. This gene has also been linked to other cancers, including androgen-independent prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":108047545,"end":108168956,"strand":-1,"description":"lymphoid enhancer binding factor 1 [Source:HGNC Symbol;Acc:HGNC:6551]"}, {"versioned_ensembl_gene_id":"ENSG00000145835.6","gene_symbol":"CDKN2AIPNLP2","gene_name":"CDKN2A interacting protein N-terminal like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128579","summary":null,"start":26827169,"end":26827520,"strand":-1,"description":"CDKN2A interacting protein N-terminal like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39855]"}, {"versioned_ensembl_gene_id":"ENSG00000164983.7","gene_symbol":"TMEM65","gene_name":"transmembrane protein 65 [Source:HGNC Symbol;Acc:HGNC:25203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"157378","summary":null,"start":124306189,"end":124372692,"strand":-1,"description":"transmembrane protein 65 [Source:HGNC Symbol;Acc:HGNC:25203]"}, {"versioned_ensembl_gene_id":"ENSG00000198798.5","gene_symbol":"MAGEB3","gene_name":"MAGE family member B3 [Source:HGNC Symbol;Acc:HGNC:6810]","synonyms":"CT3.5","biotype":"protein_coding","ncbi_id":"4114","summary":"This gene is a MAGE-B subfamily member of the MAGE gene family. MAGE family member proteins direct the expression of tumor antigens recognized on a human melanoma by autologous cytolytic T lymphocytes. There are two known clusters of MAGE genes on chromosome X. The members of the MAGE-A subfamily are located in the Xq28 region, while the members of the MAGE-B subfamily are clustered in the Xp21 region. [provided by RefSeq, Jul 2008]","start":30230436,"end":30237492,"strand":1,"description":"MAGE family member B3 [Source:HGNC Symbol;Acc:HGNC:6810]"}, {"versioned_ensembl_gene_id":"ENSG00000120289.11","gene_symbol":"MAGEB4","gene_name":"MAGE family member B4 [Source:HGNC Symbol;Acc:HGNC:6811]","synonyms":"MGC33144,CT3.6","biotype":"protein_coding","ncbi_id":"4115","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEB genes are clustered on chromosome Xp22-p21. This gene sequence ends in the first intron of MAGEB1, another family member. This gene is expressed in testis. [provided by RefSeq, Jul 2008]","start":30242052,"end":30244193,"strand":1,"description":"MAGE family member B4 [Source:HGNC Symbol;Acc:HGNC:6811]"}, {"versioned_ensembl_gene_id":"ENSG00000206422.2","gene_symbol":"LRRC30","gene_name":"leucine rich repeat containing 30 [Source:HGNC Symbol;Acc:HGNC:30219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339291","summary":null,"start":7231125,"end":7232047,"strand":1,"description":"leucine rich repeat containing 30 [Source:HGNC Symbol;Acc:HGNC:30219]"}, {"versioned_ensembl_gene_id":"ENSG00000214107.7","gene_symbol":"MAGEB1","gene_name":"MAGE family member B1 [Source:HGNC Symbol;Acc:HGNC:6808]","synonyms":"MGC9322,MAGEL1,MAGE-Xp,DAM10,CT3.1","biotype":"protein_coding","ncbi_id":"4112","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region, and expressed in testis and in a significant fraction of tumors of various histological types. This gene and other MAGEB members are clustered on chromosome Xp22-p21. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene, however, the full length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]","start":30243730,"end":30252038,"strand":1,"description":"MAGE family member B1 [Source:HGNC Symbol;Acc:HGNC:6808]"}, {"versioned_ensembl_gene_id":"ENSG00000229539.1","gene_symbol":"AL353194.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3888239,"end":3888868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234455.1","gene_symbol":"AC067960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121081437,"end":121088726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226298.1","gene_symbol":"RAD23BP3","gene_name":"RAD23 homolog B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9814]","synonyms":"RAD23BLP","biotype":"processed_pseudogene","ncbi_id":"54034","summary":null,"start":15694300,"end":15696581,"strand":-1,"description":"RAD23 homolog B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9814]"}, {"versioned_ensembl_gene_id":"ENSG00000260392.5","gene_symbol":"AC090518.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":56542952,"end":56629592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250190.1","gene_symbol":"LINC02364","gene_name":"long intergenic non-protein coding RNA 2364 [Source:HGNC Symbol;Acc:HGNC:53288]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723764","summary":null,"start":28996524,"end":29014594,"strand":1,"description":"long intergenic non-protein coding RNA 2364 [Source:HGNC Symbol;Acc:HGNC:53288]"}, {"versioned_ensembl_gene_id":"ENSG00000103126.14","gene_symbol":"AXIN1","gene_name":"axin 1 [Source:HGNC Symbol;Acc:HGNC:903]","synonyms":"PPP1R49","biotype":"protein_coding","ncbi_id":"8312","summary":"This gene encodes a cytoplasmic protein which contains a regulation of G-protein signaling (RGS) domain and a dishevelled and axin (DIX) domain. The encoded protein interacts with adenomatosis polyposis coli, catenin beta-1, glycogen synthase kinase 3 beta, protein phosphate 2, and itself. This protein functions as a negative regulator of the wingless-type MMTV integration site family, member 1 (WNT) signaling pathway and can induce apoptosis. The crystal structure of a portion of this protein, alone and in a complex with other proteins, has been resolved. Mutations in this gene have been associated with hepatocellular carcinoma, hepatoblastomas, ovarian endometriod adenocarcinomas, and medullablastomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":287440,"end":352673,"strand":-1,"description":"axin 1 [Source:HGNC Symbol;Acc:HGNC:903]"}, {"versioned_ensembl_gene_id":"ENSG00000248872.1","gene_symbol":"LINC02431","gene_name":"long intergenic non-protein coding RNA 2431 [Source:HGNC Symbol;Acc:HGNC:53362]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506122","summary":null,"start":171040602,"end":171059163,"strand":1,"description":"long intergenic non-protein coding RNA 2431 [Source:HGNC Symbol;Acc:HGNC:53362]"}, {"versioned_ensembl_gene_id":"ENSG00000276940.1","gene_symbol":"PLCE1P1","gene_name":"phospholipase C epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51906]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420075","summary":null,"start":30290047,"end":30290351,"strand":-1,"description":"phospholipase C epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51906]"}, {"versioned_ensembl_gene_id":"ENSG00000169297.7","gene_symbol":"NR0B1","gene_name":"nuclear receptor subfamily 0 group B member 1 [Source:HGNC Symbol;Acc:HGNC:7960]","synonyms":"DSS,DAX1,AHCH,AHC","biotype":"protein_coding","ncbi_id":"190","summary":"This gene encodes a protein that contains a DNA-binding domain. The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor. This protein also functions as an anti-testis gene by acting antagonistically to Sry. Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. [provided by RefSeq, Jul 2008]","start":30304206,"end":30309598,"strand":-1,"description":"nuclear receptor subfamily 0 group B member 1 [Source:HGNC Symbol;Acc:HGNC:7960]"}, {"versioned_ensembl_gene_id":"ENSG00000249525.1","gene_symbol":"AC034159.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171113789,"end":171114581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145246.13","gene_symbol":"ATP10D","gene_name":"ATPase phospholipid transporting 10D (putative) [Source:HGNC Symbol;Acc:HGNC:13549]","synonyms":"KIAA1487,ATPVD","biotype":"protein_coding","ncbi_id":"57205","summary":null,"start":47485288,"end":47593486,"strand":1,"description":"ATPase phospholipid transporting 10D (putative) [Source:HGNC Symbol;Acc:HGNC:13549]"}, {"versioned_ensembl_gene_id":"ENSG00000265206.5","gene_symbol":"AC004687.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58330884,"end":58332508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273230.1","gene_symbol":"AC102953.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1464497,"end":1467522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228257.1","gene_symbol":"AC010141.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21531839,"end":21534011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166482.11","gene_symbol":"MFAP4","gene_name":"microfibril associated protein 4 [Source:HGNC Symbol;Acc:HGNC:7035]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4239","summary":"This gene encodes a protein with similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":19383442,"end":19387240,"strand":-1,"description":"microfibril associated protein 4 [Source:HGNC Symbol;Acc:HGNC:7035]"}, {"versioned_ensembl_gene_id":"ENSG00000005379.15","gene_symbol":"TSPOAP1","gene_name":"TSPO associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16831]","synonyms":"PRAX-1,KIAA0612,BZRAP1,RIMBP1,RIM-BP1","biotype":"protein_coding","ncbi_id":"9256","summary":null,"start":58301228,"end":58328760,"strand":-1,"description":"TSPO associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16831]"}, {"versioned_ensembl_gene_id":"ENSG00000234414.7","gene_symbol":"RBMY1A1","gene_name":"RNA binding motif protein, Y-linked, family 1, member A1 [Source:HGNC Symbol;Acc:HGNC:9912]","synonyms":"YRRM2,YRRM1,RBM2,RBM1","biotype":"protein_coding","ncbi_id":"5940","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein is thought to function as a splicing regulator during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":21511372,"end":21549326,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member A1 [Source:HGNC Symbol;Acc:HGNC:9912]"}, {"versioned_ensembl_gene_id":"ENSG00000251080.1","gene_symbol":"AC024132.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27133996,"end":27140051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075336.11","gene_symbol":"TIMM21","gene_name":"translocase of inner mitochondrial membrane 21 [Source:HGNC Symbol;Acc:HGNC:25010]","synonyms":"TIM21,HSPC154,C18orf55","biotype":"protein_coding","ncbi_id":"29090","summary":null,"start":74148511,"end":74160530,"strand":1,"description":"translocase of inner mitochondrial membrane 21 [Source:HGNC Symbol;Acc:HGNC:25010]"}, {"versioned_ensembl_gene_id":"ENSG00000238045.9","gene_symbol":"AC009133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29808636,"end":29821252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251325.1","gene_symbol":"AC024132.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27262506,"end":27267254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120280.5","gene_symbol":"CXorf21","gene_name":"chromosome X open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:25667]","synonyms":"FLJ11577","biotype":"protein_coding","ncbi_id":"80231","summary":null,"start":30558824,"end":30577844,"strand":-1,"description":"chromosome X open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:25667]"}, {"versioned_ensembl_gene_id":"ENSG00000205830.1","gene_symbol":"AC024132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27207505,"end":27218404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268061.5","gene_symbol":"NAPA-AS1","gene_name":"NAPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44118]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505681","summary":null,"start":47484282,"end":47501597,"strand":1,"description":"NAPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44118]"}, {"versioned_ensembl_gene_id":"ENSG00000235865.2","gene_symbol":"GSN-AS1","gene_name":"GSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23372]","synonyms":"MOST2,C9orf31","biotype":"antisense_RNA","ncbi_id":"57000","summary":null,"start":121280768,"end":121285530,"strand":-1,"description":"GSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23372]"}, {"versioned_ensembl_gene_id":"ENSG00000249699.1","gene_symbol":"LINC02261","gene_name":"long intergenic non-protein coding RNA 2261 [Source:HGNC Symbol;Acc:HGNC:53173]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929199","summary":null,"start":27217479,"end":27282225,"strand":1,"description":"long intergenic non-protein coding RNA 2261 [Source:HGNC Symbol;Acc:HGNC:53173]"}, {"versioned_ensembl_gene_id":"ENSG00000214651.4","gene_symbol":"AL513122.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121238117,"end":121240089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277789.4","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160591,"end":54173655,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000174792.10","gene_symbol":"C4orf26","gene_name":"chromosome 4 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:26300]","synonyms":"FLJ23657,AI2A4","biotype":"protein_coding","ncbi_id":"152816","summary":"Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene is thought to encode an extracellular matrix acidic phosphoprotein that has a function in enamel mineralization during amelogenesis. Mutations in this gene are associated with recessive hypomineralized amelogenesis imperfecta. [provided by RefSeq, Oct 2012]","start":75556048,"end":75565885,"strand":1,"description":"chromosome 4 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:26300]"}, {"versioned_ensembl_gene_id":"ENSG00000237886.1","gene_symbol":"NALT1","gene_name":"NOTCH1 associated lncRNA in T-cell acute lymphoblastic leukemia 1 [Source:HGNC Symbol;Acc:HGNC:51192]","synonyms":"TCONS_l2_00029132,MIR4674HG,LINC01573","biotype":"antisense_RNA","ncbi_id":"101928483","summary":null,"start":136546212,"end":136549893,"strand":1,"description":"NOTCH1 associated lncRNA in T-cell acute lymphoblastic leukemia 1 [Source:HGNC Symbol;Acc:HGNC:51192]"}, {"versioned_ensembl_gene_id":"ENSG00000279861.1","gene_symbol":"AC073548.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47487638,"end":47489519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250858.1","gene_symbol":"IGBP1P5","gene_name":"immunoglobulin (CD79A) binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391642","summary":null,"start":27585145,"end":27586144,"strand":1,"description":"immunoglobulin (CD79A) binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43614]"}, {"versioned_ensembl_gene_id":"ENSG00000181458.10","gene_symbol":"TMEM45A","gene_name":"transmembrane protein 45A [Source:HGNC Symbol;Acc:HGNC:25480]","synonyms":"FLJ10134,DERP7","biotype":"protein_coding","ncbi_id":"55076","summary":null,"start":100492619,"end":100577444,"strand":1,"description":"transmembrane protein 45A [Source:HGNC Symbol;Acc:HGNC:25480]"}, {"versioned_ensembl_gene_id":"ENSG00000105402.7","gene_symbol":"NAPA","gene_name":"NSF attachment protein alpha [Source:HGNC Symbol;Acc:HGNC:7641]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8775","summary":"This gene encodes a member of the soluble NSF attachment protein (SNAP) family. SNAP proteins play a critical role in the docking and fusion of vesicles to target membranes as part of the 20S NSF-SNAP-SNARE complex. The encoded protein plays a role in the completion of membrane fusion by mediating the interaction of N-ethylmaleimide-sensitive factor (NSF) with the vesicle-associated and membrane-associated SNAP receptor (SNARE) complex, and stimulating the ATPase activity of NSF. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jun 2011]","start":47487637,"end":47515240,"strand":-1,"description":"NSF attachment protein alpha [Source:HGNC Symbol;Acc:HGNC:7641]"}, {"versioned_ensembl_gene_id":"ENSG00000279141.3","gene_symbol":"LINC01451","gene_name":"long intergenic non-protein coding RNA 1451 [Source:NCBI gene;Acc:401561]","synonyms":"HCCAT4","biotype":"lincRNA","ncbi_id":"401561","summary":null,"start":136612024,"end":136617181,"strand":-1,"description":"long intergenic non-protein coding RNA 1451 [Source:NCBI gene;Acc:401561]"}, {"versioned_ensembl_gene_id":"ENSG00000251579.1","gene_symbol":"AC055733.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130927754,"end":130928276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251410.1","gene_symbol":"AC007106.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27967723,"end":27985063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250592.1","gene_symbol":"AC055733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130899414,"end":130929976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250038.5","gene_symbol":"AC109588.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28362279,"end":28402864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250608.1","gene_symbol":"AC010210.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":131325092,"end":131381475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225249.5","gene_symbol":"LINC00378","gene_name":"long intergenic non-protein coding RNA 378 [Source:HGNC Symbol;Acc:HGNC:42704]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926930","summary":null,"start":60685199,"end":60694528,"strand":1,"description":"long intergenic non-protein coding RNA 378 [Source:HGNC Symbol;Acc:HGNC:42704]"}, {"versioned_ensembl_gene_id":"ENSG00000153291.15","gene_symbol":"SLC25A27","gene_name":"solute carrier family 25 member 27 [Source:HGNC Symbol;Acc:HGNC:21065]","synonyms":"UCP4,FLJ33552","biotype":"protein_coding","ncbi_id":"9481","summary":"Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. Transcripts of this gene are only detected in brain tissue and are specifically modulated by various environmental conditions. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]","start":46652915,"end":46678193,"strand":1,"description":"solute carrier family 25 member 27 [Source:HGNC Symbol;Acc:HGNC:21065]"}, {"versioned_ensembl_gene_id":"ENSG00000284095.1","gene_symbol":"AC055733.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130868004,"end":130869357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167945.1","gene_symbol":"PRR25","gene_name":"proline rich 25 [Source:HGNC Symbol;Acc:HGNC:37230]","synonyms":"gs64","biotype":"protein_coding","ncbi_id":"388199","summary":null,"start":805443,"end":813861,"strand":1,"description":"proline rich 25 [Source:HGNC Symbol;Acc:HGNC:37230]"}, {"versioned_ensembl_gene_id":"ENSG00000249098.1","gene_symbol":"AC055733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130918226,"end":130919120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275438.1","gene_symbol":"AL031008.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":848525,"end":849065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279657.1","gene_symbol":"AL161901.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":60730176,"end":60733600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158482.10","gene_symbol":"SNX29P1","gene_name":"sorting nexin 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31913]","synonyms":"RUNDC2B","biotype":"unprocessed_pseudogene","ncbi_id":"100652781","summary":null,"start":21376648,"end":21386064,"strand":1,"description":"sorting nexin 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31913]"}, {"versioned_ensembl_gene_id":"ENSG00000250064.1","gene_symbol":"AC097480.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28435449,"end":28600275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228401.4","gene_symbol":"HSPC324","gene_name":"uncharacterized LOC101928612 [Source:NCBI gene;Acc:101928612]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928612","summary":null,"start":136648610,"end":136660421,"strand":-1,"description":"uncharacterized LOC101928612 [Source:NCBI gene;Acc:101928612]"}, {"versioned_ensembl_gene_id":"ENSG00000268531.3","gene_symbol":"AC060814.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21368459,"end":21370621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166033.11","gene_symbol":"HTRA1","gene_name":"HtrA serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:9476]","synonyms":"HtrA,ARMD7,PRSS11,IGFBP5-protease","biotype":"protein_coding","ncbi_id":"5654","summary":"This gene encodes a member of the trypsin family of serine proteases. This protein is a secreted enzyme that is proposed to regulate the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins. It has also been suggested to be a regulator of cell growth. Variations in the promoter region of this gene are the cause of susceptibility to age-related macular degeneration type 7. [provided by RefSeq, Jul 2008]","start":122461525,"end":122514908,"strand":1,"description":"HtrA serine peptidase 1 [Source:HGNC Symbol;Acc:HGNC:9476]"}, {"versioned_ensembl_gene_id":"ENSG00000227510.3","gene_symbol":"LINC01442","gene_name":"long intergenic non-protein coding RNA 1442 [Source:HGNC Symbol;Acc:HGNC:50764]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103456507","summary":null,"start":60917001,"end":60941768,"strand":1,"description":"long intergenic non-protein coding RNA 1442 [Source:HGNC Symbol;Acc:HGNC:50764]"}, {"versioned_ensembl_gene_id":"ENSG00000262879.5","gene_symbol":"AC068152.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46984045,"end":47100323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228797.2","gene_symbol":"FAM207BP","gene_name":"family with sequence similarity 207 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729535","summary":null,"start":18697003,"end":18697507,"strand":1,"description":"family with sequence similarity 207 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39715]"}, {"versioned_ensembl_gene_id":"ENSG00000231004.2","gene_symbol":"CECR9","gene_name":"cat eye syndrome chromosome region, candidate 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1847]","synonyms":null,"biotype":"TEC","ncbi_id":"30847","summary":null,"start":17329034,"end":17329232,"strand":1,"description":"cat eye syndrome chromosome region, candidate 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1847]"}, {"versioned_ensembl_gene_id":"ENSG00000172889.15","gene_symbol":"EGFL7","gene_name":"EGF like domain multiple 7 [Source:HGNC Symbol;Acc:HGNC:20594]","synonyms":"ZNEU1","biotype":"protein_coding","ncbi_id":"51162","summary":"This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":136658856,"end":136672678,"strand":1,"description":"EGF like domain multiple 7 [Source:HGNC Symbol;Acc:HGNC:20594]"}, {"versioned_ensembl_gene_id":"ENSG00000230931.2","gene_symbol":"GXYLT1P1","gene_name":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101111","summary":null,"start":18724415,"end":18724904,"strand":-1,"description":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]"}, {"versioned_ensembl_gene_id":"ENSG00000271315.1","gene_symbol":"AC174048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16149251,"end":16149394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250927.1","gene_symbol":"MESTP3","gene_name":"mesoderm specific transcript pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645641","summary":null,"start":28823244,"end":28824211,"strand":-1,"description":"mesoderm specific transcript pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38553]"}, {"versioned_ensembl_gene_id":"ENSG00000182574.8","gene_symbol":"Z97985.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100956593,"end":100957538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231331.1","gene_symbol":"AC103563.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94953161,"end":94953593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140545.14","gene_symbol":"MFGE8","gene_name":"milk fat globule-EGF factor 8 protein [Source:HGNC Symbol;Acc:HGNC:7036]","synonyms":"OAcGD3S,MFG-E8,HsT19888,hP47,EDIL1,BA46,SPAG10,SED1","biotype":"protein_coding","ncbi_id":"4240","summary":"This gene encodes a preproprotein that is proteolytically processed to form multiple protein products. The major encoded protein product, lactadherin, is a membrane glycoprotein that promotes phagocytosis of apoptotic cells. This protein has also been implicated in wound healing, autoimmune disease, and cancer. Lactadherin can be further processed to form a smaller cleavage product, medin, which comprises the major protein component of aortic medial amyloid (AMA). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":88898683,"end":88913411,"strand":-1,"description":"milk fat globule-EGF factor 8 protein [Source:HGNC Symbol;Acc:HGNC:7036]"}, {"versioned_ensembl_gene_id":"ENSG00000134222.16","gene_symbol":"PSRC1","gene_name":"proline and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24472]","synonyms":"DDA3","biotype":"protein_coding","ncbi_id":"84722","summary":"This gene encodes a proline-rich protein that is a target for regulation by the tumor suppressor protein p53. The encoded protein plays an important role in mitosis by recruiting and regulating microtubule depolymerases that destabalize microtubules. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Apr 2014]","start":109279556,"end":109283186,"strand":-1,"description":"proline and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24472]"}, {"versioned_ensembl_gene_id":"ENSG00000099800.7","gene_symbol":"TIMM13","gene_name":"translocase of inner mitochondrial membrane 13 [Source:HGNC Symbol;Acc:HGNC:11816]","synonyms":"TIMM13B,Tim13","biotype":"protein_coding","ncbi_id":"26517","summary":"This gene encodes a member of the evolutionarily conserved TIMM (translocase of inner mitochondrial membrane) family of proteins that function as chaperones in the import of proteins from the cytoplasm into the mitochondrial inner membrane. Proteins of this family play a role in collecting substrate proteins from the translocase of the outer mitochondrial membrane (TOM) complex and delivering them to either the sorting and assembly machinery in the outer mitochondrial membrane (SAM) complex or the TIMM22 complex in the inner mitochondrial membrane. The encoded protein and the translocase of mitochondrial inner membrane 8a protein form a 70 kDa complex in the intermembrane space. [provided by RefSeq, Jul 2013]","start":2425624,"end":2427894,"strand":-1,"description":"translocase of inner mitochondrial membrane 13 [Source:HGNC Symbol;Acc:HGNC:11816]"}, {"versioned_ensembl_gene_id":"ENSG00000242875.6","gene_symbol":"RBMY1B","gene_name":"RNA binding motif protein, Y-linked, family 1, member B [Source:HGNC Symbol;Acc:HGNC:23914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378948","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein likely functions as a splicing factor during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":21511338,"end":21549094,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member B [Source:HGNC Symbol;Acc:HGNC:23914]"}, {"versioned_ensembl_gene_id":"ENSG00000084764.10","gene_symbol":"MAPRE3","gene_name":"microtubule associated protein RP/EB family member 3 [Source:HGNC Symbol;Acc:HGNC:6892]","synonyms":"RP3,EB3","biotype":"protein_coding","ncbi_id":"22924","summary":" The protein encoded by this gene is a member of the RP/EB family of genes. The protein localizes to the cytoplasmic microtubule network and binds APCL, a homolog of the adenomatous polyposis coli tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":26970612,"end":27027196,"strand":1,"description":"microtubule associated protein RP/EB family member 3 [Source:HGNC Symbol;Acc:HGNC:6892]"}, {"versioned_ensembl_gene_id":"ENSG00000244155.1","gene_symbol":"CYP4F34P","gene_name":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]","synonyms":"CYP4F-se7[6:7:8]","biotype":"unprocessed_pseudogene","ncbi_id":"100422247","summary":null,"start":18741730,"end":18742718,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]"}, {"versioned_ensembl_gene_id":"ENSG00000179673.4","gene_symbol":"RPRML","gene_name":"reprimo like [Source:HGNC Symbol;Acc:HGNC:32422]","synonyms":"MGC43894","biotype":"protein_coding","ncbi_id":"388394","summary":null,"start":46978156,"end":46979248,"strand":-1,"description":"reprimo like [Source:HGNC Symbol;Acc:HGNC:32422]"}, {"versioned_ensembl_gene_id":"ENSG00000164932.12","gene_symbol":"CTHRC1","gene_name":"collagen triple helix repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:18831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115908","summary":"This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":103371515,"end":103382997,"strand":1,"description":"collagen triple helix repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:18831]"}, {"versioned_ensembl_gene_id":"ENSG00000263142.5","gene_symbol":"LRRC37A17P","gene_name":"leucine rich repeat containing 37 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48365]","synonyms":"LRRC37A5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644397","summary":null,"start":46978481,"end":47054569,"strand":1,"description":"leucine rich repeat containing 37 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:48365]"}, {"versioned_ensembl_gene_id":"ENSG00000277377.4","gene_symbol":"SERPINA1","gene_name":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]","synonyms":"alpha-1-antitrypsin,AAT,A1AT,A1A,PI1,PI,alpha1AT","biotype":"protein_coding","ncbi_id":"5265","summary":"The protein encoded by this gene is a serine protease inhibitor belonging to the serpin superfamily whose targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, and plasminogen activator. This protein is produced in the liver, the bone marrow, by lymphocytic and monocytic cells in lymphoid tissue, and by the Paneth cells of the gut. Defects in this gene are associated with chronic obstructive pulmonary disease, emphysema, and chronic liver disease. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2020]","start":94378757,"end":94392703,"strand":-1,"description":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]"}, {"versioned_ensembl_gene_id":"ENSG00000256232.1","gene_symbol":"LINC02387","gene_name":"long intergenic non-protein coding RNA 2387 [Source:HGNC Symbol;Acc:HGNC:53313]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929027","summary":null,"start":31363481,"end":31369301,"strand":-1,"description":"long intergenic non-protein coding RNA 2387 [Source:HGNC Symbol;Acc:HGNC:53313]"}, {"versioned_ensembl_gene_id":"ENSG00000227568.1","gene_symbol":"SNX18P26","gene_name":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419038","summary":null,"start":18807279,"end":18808018,"strand":-1,"description":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]"}, {"versioned_ensembl_gene_id":"ENSG00000020181.17","gene_symbol":"ADGRA2","gene_name":"adhesion G protein-coupled receptor A2 [Source:HGNC Symbol;Acc:HGNC:17849]","synonyms":"TEM5,KIAA1531,GPR124,FLJ14390,DKFZp434J0911,DKFZp434C211","biotype":"protein_coding","ncbi_id":"25960","summary":null,"start":37784191,"end":37844896,"strand":1,"description":"adhesion G protein-coupled receptor A2 [Source:HGNC Symbol;Acc:HGNC:17849]"}, {"versioned_ensembl_gene_id":"ENSG00000230194.1","gene_symbol":"AC000081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19238443,"end":19238739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178297.12","gene_symbol":"TMPRSS9","gene_name":"transmembrane protease, serine 9 [Source:HGNC Symbol;Acc:HGNC:30079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"360200","summary":"The protein encoded by this gene is a membrane-bound type II serine polyprotease that is cleaved to release three different proteases. Two of the proteases are active and can be inhibited by serine protease inhibitors, and one is thought to be catalytically inactive. This gene enhances the invasive capability of pancreatic cancer cells and may be involved in cancer progression. [provided by RefSeq, Jul 2016]","start":2389771,"end":2426239,"strand":1,"description":"transmembrane protease, serine 9 [Source:HGNC Symbol;Acc:HGNC:30079]"}, {"versioned_ensembl_gene_id":"ENSG00000262633.2","gene_symbol":"AC005670.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46923133,"end":47049932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186732.13","gene_symbol":"MPPED1","gene_name":"metallophosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1306]","synonyms":"C22orf1,239AB,FAM1A","biotype":"protein_coding","ncbi_id":"758","summary":null,"start":43411196,"end":43507848,"strand":1,"description":"metallophosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1306]"}, {"versioned_ensembl_gene_id":"ENSG00000284666.1","gene_symbol":"Z98259.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5480787,"end":5482028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260972.1","gene_symbol":"Z98259.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5492978,"end":5494674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284692.1","gene_symbol":"Z98259.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5478736,"end":5493057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236145.1","gene_symbol":"AC079988.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121178327,"end":121182580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108433.16","gene_symbol":"GOSR2","gene_name":"golgi SNAP receptor complex member 2 [Source:HGNC Symbol;Acc:HGNC:4431]","synonyms":"GS27,Bos1","biotype":"protein_coding","ncbi_id":"9570","summary":"This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. [provided by RefSeq, Mar 2016]","start":46923075,"end":46975524,"strand":1,"description":"golgi SNAP receptor complex member 2 [Source:HGNC Symbol;Acc:HGNC:4431]"}, {"versioned_ensembl_gene_id":"ENSG00000267239.1","gene_symbol":"AP001198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13203774,"end":13216367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169764.15","gene_symbol":"UGP2","gene_name":"UDP-glucose pyrophosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:12527]","synonyms":"UGPP1,UGP1","biotype":"protein_coding","ncbi_id":"7360","summary":"The enzyme encoded by this gene is an important intermediary in mammalian carbohydrate interconversions. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP-glucose and MgPPi. In liver and muscle tissue, UDP-glucose is a direct precursor of glycogen; in lactating mammary gland it is converted to UDP-galactose which is then converted to lactose. The eukaryotic enzyme has no significant sequence similarity to the prokaryotic enzyme. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63840940,"end":63891562,"strand":1,"description":"UDP-glucose pyrophosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:12527]"}, {"versioned_ensembl_gene_id":"ENSG00000283356.1","gene_symbol":"Z97988.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5554747,"end":5554881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248254.1","gene_symbol":"AC107398.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47556731,"end":47560259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242431.2","gene_symbol":"AC107398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47490967,"end":47491471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225016.1","gene_symbol":"LINC00328-2P","gene_name":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]","synonyms":"NCRNA00328B,NCRNA00328-2P","biotype":"processed_pseudogene","ncbi_id":"100874404","summary":null,"start":18809830,"end":18810048,"strand":1,"description":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]"}, {"versioned_ensembl_gene_id":"ENSG00000236948.2","gene_symbol":"AL365255.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5561709,"end":5668295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232594.1","gene_symbol":"AC103563.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94961047,"end":94961503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183665.5","gene_symbol":"TRMT12","gene_name":"tRNA methyltransferase 12 homolog [Source:HGNC Symbol;Acc:HGNC:26091]","synonyms":"TYW2,Trm12,FLJ20772","biotype":"protein_coding","ncbi_id":"55039","summary":"Wybutosine (yW) is a hypermodified guanosine at the 3-prime position adjacent to the anticodon of phenylalanine tRNA that stabilizes codon-anticodon interactions during decoding on the ribosome. TRMT12 is the human homolog of a yeast gene essential for yW synthesis (Noma and Suzuki, 2006).[supplied by OMIM, Mar 2008]","start":124450820,"end":124462150,"strand":1,"description":"tRNA methyltransferase 12 homolog [Source:HGNC Symbol;Acc:HGNC:26091]"}, {"versioned_ensembl_gene_id":"ENSG00000115112.7","gene_symbol":"TFCP2L1","gene_name":"transcription factor CP2 like 1 [Source:HGNC Symbol;Acc:HGNC:17925]","synonyms":"LBP-9,CRTR1","biotype":"protein_coding","ncbi_id":"29842","summary":null,"start":121216587,"end":121285207,"strand":-1,"description":"transcription factor CP2 like 1 [Source:HGNC Symbol;Acc:HGNC:17925]"}, {"versioned_ensembl_gene_id":"ENSG00000206192.7","gene_symbol":"ANKRD20A9P","gene_name":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"284232","summary":null,"start":18816718,"end":18871967,"strand":-1,"description":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]"}, {"versioned_ensembl_gene_id":"ENSG00000248989.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"bPG116M5.10,STK19P,RP2","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":32005925,"end":32006441,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000182162.10","gene_symbol":"P2RY8","gene_name":"purinergic receptor P2Y8 [Source:HGNC Symbol;Acc:HGNC:15524]","synonyms":"P2Y8","biotype":"protein_coding","ncbi_id":"286530","summary":"The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene is moderately expressed in undifferentiated HL60 cells, and is located on both chromosomes X and Y. [provided by RefSeq, Jul 2008]","start":1462572,"end":1537107,"strand":-1,"description":"purinergic receptor P2Y8 [Source:HGNC Symbol;Acc:HGNC:15524]"}, {"versioned_ensembl_gene_id":"ENSG00000245149.3","gene_symbol":"RNF139-AS1","gene_name":"RNF139 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48940]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927612","summary":null,"start":124462485,"end":124474576,"strand":-1,"description":"RNF139 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48940]"}, {"versioned_ensembl_gene_id":"ENSG00000280165.1","gene_symbol":"PCDH20","gene_name":"protocadherin 20 [Source:HGNC Symbol;Acc:HGNC:14257]","synonyms":"PCDH13,FLJ22218","biotype":"protein_coding","ncbi_id":"64881","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. This gene encodes a protein which contains 6 extracellular cadherin domains, a transmembrane domain and a cytoplasmic tail differing from those of the classical cadherins. Although its specific function is undetermined, the cadherin-related neuronal receptor is thought to play a role in the establishment and function of specific cell-cell connections in the brain. [provided by RefSeq, Jul 2008]","start":61409685,"end":61415522,"strand":-1,"description":"protocadherin 20 [Source:HGNC Symbol;Acc:HGNC:14257]"}, {"versioned_ensembl_gene_id":"ENSG00000237301.1","gene_symbol":"AL121992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15586136,"end":15603626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279797.1","gene_symbol":"LINC02339","gene_name":"long intergenic non-protein coding RNA 2339 [Source:HGNC Symbol;Acc:HGNC:53259]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926951","summary":null,"start":61424689,"end":61427946,"strand":-1,"description":"long intergenic non-protein coding RNA 2339 [Source:HGNC Symbol;Acc:HGNC:53259]"}, {"versioned_ensembl_gene_id":"ENSG00000116771.5","gene_symbol":"AGMAT","gene_name":"agmatinase [Source:HGNC Symbol;Acc:HGNC:18407]","synonyms":"FLJ23384","biotype":"protein_coding","ncbi_id":"79814","summary":null,"start":15572353,"end":15585110,"strand":-1,"description":"agmatinase [Source:HGNC Symbol;Acc:HGNC:18407]"}, {"versioned_ensembl_gene_id":"ENSG00000176619.12","gene_symbol":"LMNB2","gene_name":"lamin B2 [Source:HGNC Symbol;Acc:HGNC:6638]","synonyms":"LMN2","biotype":"protein_coding","ncbi_id":"84823","summary":"This gene encodes a B type nuclear lamin. The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Mutations in this gene are associated with acquired partial lipodystrophy. [provided by RefSeq, May 2012]","start":2427638,"end":2456996,"strand":-1,"description":"lamin B2 [Source:HGNC Symbol;Acc:HGNC:6638]"}, {"versioned_ensembl_gene_id":"ENSG00000197991.11","gene_symbol":"AL592490.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61409858,"end":61427849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172113.8","gene_symbol":"NME6","gene_name":"NME/NM23 nucleoside diphosphate kinase 6 [Source:HGNC Symbol;Acc:HGNC:20567]","synonyms":"NM23-H6,IPIA-ALPHA","biotype":"protein_coding","ncbi_id":"10201","summary":"Nucleoside diphosphate (NDP) kinases (EC 2.7.4.6), such as NME6, are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates (Mehus et al., 1999 [PubMed 10453732]).[supplied by OMIM, Jul 2010]","start":48293264,"end":48301685,"strand":-1,"description":"NME/NM23 nucleoside diphosphate kinase 6 [Source:HGNC Symbol;Acc:HGNC:20567]"}, {"versioned_ensembl_gene_id":"ENSG00000256263.1","gene_symbol":"DDX11L8","gene_name":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100302090","summary":null,"start":12310,"end":13501,"strand":1,"description":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]"}, {"versioned_ensembl_gene_id":"ENSG00000228520.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33186401,"end":33190628,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000223923.1","gene_symbol":"AC010136.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":217978707,"end":217992615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233105.1","gene_symbol":"AC103563.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94964473,"end":94964836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262411.1","gene_symbol":"LINC02066","gene_name":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374158","summary":null,"start":151637174,"end":151657956,"strand":1,"description":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]"}, {"versioned_ensembl_gene_id":"ENSG00000136936.10","gene_symbol":"XPA","gene_name":"XPA, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12814]","synonyms":"XPAC,XP1","biotype":"protein_coding","ncbi_id":"7507","summary":"This gene encodes a zinc finger protein plays a central role in nucleotide excision repair (NER), a specialized type of DNA repair. NER is responsible for repair of UV radiation-induced photoproducts and DNA adducts induced by chemical carcinogens and chemotherapeutic drugs. The encoded protein interacts with DNA and several NER proteins, acting as a scaffold to assemble the NER incision complex at sites of DNA damage. Mutations in this gene cause Xeroderma pigmentosum complementation group A (XP-A), an autosomal recessive skin disorder featuring hypersensitivity to sunlight and increased risk for skin cancer. [provided by RefSeq, Aug 2017]","start":97674909,"end":97697357,"strand":-1,"description":"XPA, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12814]"}, {"versioned_ensembl_gene_id":"ENSG00000249228.1","gene_symbol":"AC068944.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29046591,"end":29048765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181803.3","gene_symbol":"OR6S1","gene_name":"olfactory receptor family 6 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15363]","synonyms":"OR6S1Q","biotype":"protein_coding","ncbi_id":"341799","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20640696,"end":20641691,"strand":-1,"description":"olfactory receptor family 6 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15363]"}, {"versioned_ensembl_gene_id":"ENSG00000248176.1","gene_symbol":"AC109349.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29118308,"end":29202770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168874.12","gene_symbol":"ATOH8","gene_name":"atonal bHLH transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24126]","synonyms":"bHLHa21,FLJ14708,HATH6","biotype":"protein_coding","ncbi_id":"84913","summary":null,"start":85751344,"end":85788066,"strand":1,"description":"atonal bHLH transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24126]"}, {"versioned_ensembl_gene_id":"ENSG00000224585.1","gene_symbol":"AC103563.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94971954,"end":94972167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248338.1","gene_symbol":"LINC02472","gene_name":"long intergenic non-protein coding RNA 2472 [Source:HGNC Symbol;Acc:HGNC:53411]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374561","summary":null,"start":29214398,"end":29221162,"strand":1,"description":"long intergenic non-protein coding RNA 2472 [Source:HGNC Symbol;Acc:HGNC:53411]"}, {"versioned_ensembl_gene_id":"ENSG00000251373.1","gene_symbol":"AC092593.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29407100,"end":29408012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276548.1","gene_symbol":"AC008740.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21401089,"end":21401198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186714.12","gene_symbol":"CCDC73","gene_name":"coiled-coil domain containing 73 [Source:HGNC Symbol;Acc:HGNC:23261]","synonyms":"NY-SAR-79","biotype":"protein_coding","ncbi_id":"493860","summary":null,"start":32602246,"end":32794658,"strand":-1,"description":"coiled-coil domain containing 73 [Source:HGNC Symbol;Acc:HGNC:23261]"}, {"versioned_ensembl_gene_id":"ENSG00000233447.1","gene_symbol":"AC103563.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94974544,"end":94974838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160072.19","gene_symbol":"ATAD3B","gene_name":"ATPase family, AAA domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24007]","synonyms":"TOB3,KIAA1273","biotype":"protein_coding","ncbi_id":"83858","summary":"The protein encoded by this gene is localized to the mitochondrial inner membrane, where it can bind to a highly-related protein, ATAD3A. ATAD3A appears to interact with matrix nucleoid complexes, and the encoded protein negatively regulates that interaction. This gene is expressed almost exclusively in pluripotent embryonic stem cells and some cancer cells. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":1471769,"end":1497848,"strand":1,"description":"ATPase family, AAA domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24007]"}, {"versioned_ensembl_gene_id":"ENSG00000235186.1","gene_symbol":"AC103563.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94991880,"end":94994362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259171.1","gene_symbol":"AL163636.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":20684587,"end":20700576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272501.1","gene_symbol":"AL662844.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31195200,"end":31198037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251113.2","gene_symbol":"AC092593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29465701,"end":29467850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206344.7","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"lincRNA","ncbi_id":"253018","summary":null,"start":31197760,"end":31203968,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000105711.11","gene_symbol":"SCN1B","gene_name":"sodium voltage-gated channel beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:10586]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6324","summary":"Voltage-gated sodium channels are heteromeric proteins that function in the generation and propagation of action potentials in muscle and neuronal cells. They are composed of one alpha and two beta subunits, where the alpha subunit provides channel activity and the beta-1 subunit modulates the kinetics of channel inactivation. This gene encodes a sodium channel beta-1 subunit. Mutations in this gene result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":35030466,"end":35040449,"strand":1,"description":"sodium voltage-gated channel beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:10586]"}, {"versioned_ensembl_gene_id":"ENSG00000214274.9","gene_symbol":"ANG","gene_name":"angiogenin [Source:HGNC Symbol;Acc:HGNC:483]","synonyms":"RNASE5,RAA1","biotype":"protein_coding","ncbi_id":"283","summary":"The protein encoded by this gene is a member of the RNase A superfamily though it has relatively weak ribonucleolytic activity. This protein is a potent mediator of new blood vessel formation and thus, in addition to the name RNase5, is commonly called angiogenin. This protein induces angiogenesis after binding to actin on the surface of endothelial cells. This protein also accumulates at the nucleolus where it stimulates ribosomal transcription. Under stress conditions this protein translocates to the cytosol where it hydrolyzes cellular tRNAs and influences protein synthesis. A signal peptide is cleaved from the precursor protein to produce a mature protein which contains a nuclear localization signal, a cell binding motif, and a catalytic domain. This protein has been shown to be both neurotrophic and neuroprotective and the mature protein has antimicrobial activity against some bacteria and fungi, including S. pneumoniae and C. albicans. Due to its effect on rRNA production and angiogenesis this gene plays important roles in cell growth and tumor progression. Mutations in this gene are associated with progression of amyotrophic lateral sclerosis (ALS). This gene and the neighboring RNase4 gene share promoters and 5' exons though each gene then splices to a distinct 3' exon containing the complete coding region of each gene. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2020]","start":20684177,"end":20698971,"strand":1,"description":"angiogenin [Source:HGNC Symbol;Acc:HGNC:483]"}, {"versioned_ensembl_gene_id":"ENSG00000242756.2","gene_symbol":"RHOT1P3","gene_name":"ras homolog family member T1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37839]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462810","summary":null,"start":18837768,"end":18838098,"strand":-1,"description":"ras homolog family member T1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37839]"}, {"versioned_ensembl_gene_id":"ENSG00000248755.1","gene_symbol":"AC092639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171169209,"end":171169942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248339.1","gene_symbol":"LINC02504","gene_name":"long intergenic non-protein coding RNA 2504 [Source:HGNC Symbol;Acc:HGNC:53493]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928288","summary":null,"start":171289475,"end":171298267,"strand":-1,"description":"long intergenic non-protein coding RNA 2504 [Source:HGNC Symbol;Acc:HGNC:53493]"}, {"versioned_ensembl_gene_id":"ENSG00000272510.1","gene_symbol":"AL121992.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15565611,"end":15565956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251176.1","gene_symbol":"AC074254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":171553000,"end":171564267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228216.1","gene_symbol":"AL355607.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90957260,"end":90965393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260965.1","gene_symbol":"RPL23AP91","gene_name":"ribosomal protein L23a pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:51625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480337","summary":null,"start":57321352,"end":57322117,"strand":1,"description":"ribosomal protein L23a pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:51625]"}, {"versioned_ensembl_gene_id":"ENSG00000134588.12","gene_symbol":"USP26","gene_name":"ubiquitin specific peptidase 26 [Source:HGNC Symbol;Acc:HGNC:13485]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83844","summary":"This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases and is a deubiquitinating enzyme (DUB) with His and Cys domains. It is specifically expressed in testis tissue. Mutations in this gene have been associated with Sertoli cell-only syndrome and male infertility. [provided by RefSeq, Jul 2008]","start":133024631,"end":133097109,"strand":-1,"description":"ubiquitin specific peptidase 26 [Source:HGNC Symbol;Acc:HGNC:13485]"}, {"versioned_ensembl_gene_id":"ENSG00000082516.8","gene_symbol":"GEMIN5","gene_name":"gem nuclear organelle associated protein 5 [Source:HGNC Symbol;Acc:HGNC:20043]","synonyms":null,"biotype":"protein_coding","ncbi_id":"25929","summary":"This gene encodes a WD repeat protein that is a component of the survival of motor neurons (SMN) complex. The SMN complex plays a critical role in mRNA splicing through the assembly of spliceosomal small nuclear ribonucleoproteins (snRNPs), and may also mediate the assembly and transport of other classes of ribonucleoproteins. The encoded protein is the snRNA-binding component of the SMN complex. Dysregulation of this gene may play a role in alternative mRNA splicing and tumor cell motility. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":154887416,"end":154938209,"strand":-1,"description":"gem nuclear organelle associated protein 5 [Source:HGNC Symbol;Acc:HGNC:20043]"}, {"versioned_ensembl_gene_id":"ENSG00000271821.1","gene_symbol":"AL662844.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31200165,"end":31201918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249297.1","gene_symbol":"LINC02174","gene_name":"long intergenic non-protein coding RNA 2174 [Source:HGNC Symbol;Acc:HGNC:53037]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377536","summary":null,"start":171602683,"end":171638763,"strand":-1,"description":"long intergenic non-protein coding RNA 2174 [Source:HGNC Symbol;Acc:HGNC:53037]"}, {"versioned_ensembl_gene_id":"ENSG00000230537.1","gene_symbol":"AL158071.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91104957,"end":91107304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237036.4","gene_symbol":"ZEB1-AS1","gene_name":"ZEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42354]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"220930","summary":"This locus produces long non-coding RNA that is transcribed from a shared bi-directional promoter with zinc finger E-box binding homeobox 1 (ZEB1). This transcript binds lysine methyltransferase 2A and promotes histone modifications that are thought to promote expression of ZEB1. Expression of this gene is correlated with tumor progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":31206278,"end":31320447,"strand":-1,"description":"ZEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42354]"}, {"versioned_ensembl_gene_id":"ENSG00000104221.12","gene_symbol":"BRF2","gene_name":"BRF2, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:17298]","synonyms":"TFIIIB50,FLJ11052,BRFU","biotype":"protein_coding","ncbi_id":"55290","summary":"This gene encodes one of the multiple subunits of the RNA polymerase III transcription factor complex required for transcription of genes with promoter elements upstream of the initiation site. The product of this gene, a TFIIB-like factor, is directly recruited to the TATA-box of polymerase III small nuclear RNA gene promoters through its interaction with the TATA-binding protein. [provided by RefSeq, Jul 2008]","start":37843268,"end":37849904,"strand":-1,"description":"BRF2, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:17298]"}, {"versioned_ensembl_gene_id":"ENSG00000271456.1","gene_symbol":"AC108081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57332379,"end":57332599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233850.1","gene_symbol":"AC103563.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95025193,"end":95026709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258451.1","gene_symbol":"AL163636.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20693480,"end":20707120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231062.1","gene_symbol":"AC103563.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95051395,"end":95053176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223622.2","gene_symbol":"GSTA6P","gene_name":"glutathione S-transferase alpha 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:4630]","synonyms":"GSTAP1","biotype":"unprocessed_pseudogene","ncbi_id":"2942","summary":null,"start":52805613,"end":52813460,"strand":-1,"description":"glutathione S-transferase alpha 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:4630]"}, {"versioned_ensembl_gene_id":"ENSG00000237422.1","gene_symbol":"AL158071.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91119138,"end":91163087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274474.3","gene_symbol":"YWHAE","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]","synonyms":"FLJ45465","biotype":"protein_coding","ncbi_id":"7531","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 100% identical to the mouse ortholog. It interacts with CDC25 phosphatases, RAF1 and IRS1 proteins, suggesting its role in diverse biochemical activities related to signal transduction, such as cell division and regulation of insulin sensitivity. It has also been implicated in the pathogenesis of small cell lung cancer. Two transcript variants, one protein-coding and the other non-protein-coding, have been found for this gene. [provided by RefSeq, Aug 2008]","start":1247054,"end":1303157,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]"}, {"versioned_ensembl_gene_id":"ENSG00000258818.3","gene_symbol":"RNASE4","gene_name":"ribonuclease A family member 4 [Source:HGNC Symbol;Acc:HGNC:10047]","synonyms":"RAB1","biotype":"protein_coding","ncbi_id":"6038","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family. It plays an important role in mRNA cleavage and has marked specificity towards the 3' side of uridine nucleotides. Alternative splicing results in four transcript variants encoding the same protein. This gene and the gene that encodes angiogenin share promoters and 5' exons. Each gene splices to a unique downstream exon that contains its complete coding region. [provided by RefSeq, Aug 2013]","start":20684100,"end":20701215,"strand":1,"description":"ribonuclease A family member 4 [Source:HGNC Symbol;Acc:HGNC:10047]"}, {"versioned_ensembl_gene_id":"ENSG00000172005.10","gene_symbol":"MAL","gene_name":"mal, T-cell differentiation protein [Source:HGNC Symbol;Acc:HGNC:6817]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4118","summary":"The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]","start":95025677,"end":95053996,"strand":1,"description":"mal, T-cell differentiation protein [Source:HGNC Symbol;Acc:HGNC:6817]"}, {"versioned_ensembl_gene_id":"ENSG00000229694.6","gene_symbol":"LINC00484","gene_name":"long intergenic non-protein coding RNA 484 [Source:NCBI gene;Acc:100129347]","synonyms":"C9orf73,C9orf73","biotype":"lincRNA","ncbi_id":"100129347","summary":null,"start":91119062,"end":91182762,"strand":1,"description":"long intergenic non-protein coding RNA 484 [Source:NCBI gene;Acc:100129347]"}, {"versioned_ensembl_gene_id":"ENSG00000249998.1","gene_symbol":"AC106894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16973275,"end":17073903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251212.1","gene_symbol":"MTND5P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42306]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873200","summary":null,"start":17061878,"end":17062165,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42306]"}, {"versioned_ensembl_gene_id":"ENSG00000272381.1","gene_symbol":"AL356258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31187883,"end":31261910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244203.2","gene_symbol":"FOXP1-AS1","gene_name":"FOXP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41942]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104502416","summary":null,"start":71289769,"end":71305853,"strand":1,"description":"FOXP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41942]"}, {"versioned_ensembl_gene_id":"ENSG00000230397.1","gene_symbol":"SPTLC1P1","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39668]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100874511","summary":null,"start":31360955,"end":31361215,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39668]"}, {"versioned_ensembl_gene_id":"ENSG00000230147.2","gene_symbol":"AL158071.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91169585,"end":91170045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225949.1","gene_symbol":"Z77249.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133141300,"end":133143940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110031.12","gene_symbol":"LPXN","gene_name":"leupaxin [Source:HGNC Symbol;Acc:HGNC:14061]","synonyms":"LDPL","biotype":"protein_coding","ncbi_id":"9404","summary":"The product encoded by this gene is preferentially expressed in hematopoietic cells and belongs to the paxillin protein family. Similar to other members of this focal-adhesion-associated adaptor-protein family, it has four leucine-rich LD-motifs in the N-terminus and four LIM domains in the C-terminus. It may function in cell type-specific signaling by associating with PYK2, a member of focal adhesion kinase family. As a substrate for a tyrosine kinase in lymphoid cells, this protein may also function in, and be regulated by, tyrosine kinase activity. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jan 2009]","start":58526871,"end":58578220,"strand":-1,"description":"leupaxin [Source:HGNC Symbol;Acc:HGNC:14061]"}, {"versioned_ensembl_gene_id":"ENSG00000102962.4","gene_symbol":"CCL22","gene_name":"C-C motif chemokine ligand 22 [Source:HGNC Symbol;Acc:HGNC:10621]","synonyms":"SCYA22,MGC34554,MDC,DC/B-CK,ABCD-1,A-152E5.1,STCP-1","biotype":"protein_coding","ncbi_id":"6367","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, dendritic cells, natural killer cells and for chronically activated T lymphocytes. It also displays a mild activity for primary activated T lymphocytes and has no chemoattractant activity for neutrophils, eosinophils and resting T lymphocytes. The product of this gene binds to chemokine receptor CCR4. This chemokine may play a role in the trafficking of activated T lymphocytes to inflammatory sites and other aspects of activated T lymphocyte physiology. [provided by RefSeq, Sep 2014]","start":57358772,"end":57366190,"strand":1,"description":"C-C motif chemokine ligand 22 [Source:HGNC Symbol;Acc:HGNC:10621]"}, {"versioned_ensembl_gene_id":"ENSG00000205500.8","gene_symbol":"AC013472.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":26984776,"end":27014612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235641.4","gene_symbol":"LINC00484","gene_name":"long intergenic non-protein coding RNA 484 [Source:HGNC Symbol;Acc:HGNC:27862]","synonyms":"C9orf73,C9orf73","biotype":"lincRNA","ncbi_id":"100129347","summary":null,"start":91159573,"end":91165658,"strand":1,"description":"long intergenic non-protein coding RNA 484 [Source:HGNC Symbol;Acc:HGNC:27862]"}, {"versioned_ensembl_gene_id":"ENSG00000250819.1","gene_symbol":"LINC02493","gene_name":"long intergenic non-protein coding RNA 2493 [Source:HGNC Symbol;Acc:HGNC:53477]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929123","summary":null,"start":17171757,"end":17186059,"strand":-1,"description":"long intergenic non-protein coding RNA 2493 [Source:HGNC Symbol;Acc:HGNC:53477]"}, {"versioned_ensembl_gene_id":"ENSG00000261211.1","gene_symbol":"AL031123.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6680309,"end":6683633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152503.9","gene_symbol":"TRIM36","gene_name":"tripartite motif containing 36 [Source:HGNC Symbol;Acc:HGNC:16280]","synonyms":"RBCC728,HAPRIN,RNF98","biotype":"protein_coding","ncbi_id":"55521","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":115124762,"end":115180546,"strand":-1,"description":"tripartite motif containing 36 [Source:HGNC Symbol;Acc:HGNC:16280]"}, {"versioned_ensembl_gene_id":"ENSG00000223523.1","gene_symbol":"AC092598.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":188598791,"end":188839445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270903.1","gene_symbol":"HNRNPA3P9","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48755]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421415","summary":null,"start":32591793,"end":32592771,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48755]"}, {"versioned_ensembl_gene_id":"ENSG00000229498.1","gene_symbol":"AC105053.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85815130,"end":85825391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174325.4","gene_symbol":"DIRC1","gene_name":"disrupted in renal carcinoma 1 [Source:HGNC Symbol;Acc:HGNC:15760]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116093","summary":"Disruption of DIRC1 by translocation is associated with familial clear cell renal cancer. Overexpression of DIRC1 is associated with tumor progression and poor prognosis in gastric cancer. [provided by RefSeq, Mar 2019]","start":188734155,"end":188790104,"strand":-1,"description":"disrupted in renal carcinoma 1 [Source:HGNC Symbol;Acc:HGNC:15760]"}, {"versioned_ensembl_gene_id":"ENSG00000151651.15","gene_symbol":"ADAM8","gene_name":"ADAM metallopeptidase domain 8 [Source:HGNC Symbol;Acc:HGNC:215]","synonyms":"MS2,CD156a,CD156","biotype":"protein_coding","ncbi_id":"101","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene may be involved in cell adhesion during neurodegeneration, and it is thought to be a target for allergic respiratory diseases, including asthma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2009]","start":133262403,"end":133276868,"strand":-1,"description":"ADAM metallopeptidase domain 8 [Source:HGNC Symbol;Acc:HGNC:215]"}, {"versioned_ensembl_gene_id":"ENSG00000244535.1","gene_symbol":"AL049714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32758268,"end":32758614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267393.1","gene_symbol":"AP002439.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13362203,"end":13366243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254780.1","gene_symbol":"AC023232.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47905323,"end":47905607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233157.1","gene_symbol":"Z97055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43759199,"end":43759910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272746.1","gene_symbol":"AP005131.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":13526078,"end":13526688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230286.1","gene_symbol":"AC013472.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26950308,"end":27009807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279020.1","gene_symbol":"C18orf15","gene_name":"chromosome 18 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:26447]","synonyms":"HsT3231,FLJ31338","biotype":"TEC","ncbi_id":"147276","summary":null,"start":13239543,"end":13242076,"strand":1,"description":"chromosome 18 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:26447]"}, {"versioned_ensembl_gene_id":"ENSG00000169246.16","gene_symbol":"NPIPB3","gene_name":"nuclear pore complex interacting protein family member B3 [Source:HGNC Symbol;Acc:HGNC:28989]","synonyms":"KIAA0220,NPIPL3","biotype":"protein_coding","ncbi_id":"23117","summary":null,"start":21402237,"end":21448567,"strand":-1,"description":"nuclear pore complex interacting protein family member B3 [Source:HGNC Symbol;Acc:HGNC:28989]"}, {"versioned_ensembl_gene_id":"ENSG00000149100.12","gene_symbol":"EIF3M","gene_name":"eukaryotic translation initiation factor 3 subunit M [Source:HGNC Symbol;Acc:HGNC:24460]","synonyms":"TANGO7,PCID1,hfl-B5,GA17,FLJ29030,eIF3m","biotype":"protein_coding","ncbi_id":"10480","summary":"This gene encodes a protein that is part of the eurkaryotic translation initiation factor 3 complete (eIF-3) required for protein synthesis. Elevated levels of the encoded protein are present in cancer cell lines. Inactivation of the encoded protein has been shown to interfere with translation of herpes virus mRNAs by preventing the association of mRNAs with the ribosomes. A pseudogene of this gene is located on the X chromosome. [provided by RefSeq, Dec 2011]","start":32583798,"end":32606262,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit M [Source:HGNC Symbol;Acc:HGNC:24460]"}, {"versioned_ensembl_gene_id":"ENSG00000249542.2","gene_symbol":"EEF1A1P21","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421807","summary":null,"start":29748757,"end":29750100,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37894]"}, {"versioned_ensembl_gene_id":"ENSG00000260566.2","gene_symbol":"AC127459.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":23061406,"end":23064173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234730.1","gene_symbol":"AP001117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21566763,"end":21615437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183434.9","gene_symbol":"TFDP3","gene_name":"transcription factor Dp family member 3 [Source:HGNC Symbol;Acc:HGNC:24603]","synonyms":"HCA661,E2F-like,CT30","biotype":"protein_coding","ncbi_id":"51270","summary":"This gene encodes a member of the DP family of transcription factors. These factors heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. This protein functions as a negative regulator and inhibits the DNA binding and transcriptional activities of E2F factors.[provided by RefSeq, May 2010]","start":133216669,"end":133218348,"strand":-1,"description":"transcription factor Dp family member 3 [Source:HGNC Symbol;Acc:HGNC:24603]"}, {"versioned_ensembl_gene_id":"ENSG00000186976.14","gene_symbol":"EFCAB6","gene_name":"EF-hand calcium binding domain 6 [Source:HGNC Symbol;Acc:HGNC:24204]","synonyms":"dJ185D5.1,KIAA1672,HSCBCIP1,FLJ23588,DJBP","biotype":"protein_coding","ncbi_id":"64800","summary":"This gene encodes a protein which directly binds the oncogene DJ-1 and androgen receptor to form a ternary complex in cells. This binding protein recruits histone-deacetylase complexes in order to repress transcription activity of androgen receptor. This protein may also play a role in spermatogenesis and fertilization. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":43528744,"end":43812337,"strand":-1,"description":"EF-hand calcium binding domain 6 [Source:HGNC Symbol;Acc:HGNC:24204]"}, {"versioned_ensembl_gene_id":"ENSG00000157851.16","gene_symbol":"DPYSL5","gene_name":"dihydropyrimidinase like 5 [Source:HGNC Symbol;Acc:HGNC:20637]","synonyms":"Ulip6,CRMP5,CRMP-5,CRAM","biotype":"protein_coding","ncbi_id":"56896","summary":"This gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development. Antibodies to the encoded protein were found in some patients with neurologic symptoms who had paraneoplastic syndrome. A pseudogene of this gene is found on chromosome 11. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011]","start":26847747,"end":26950351,"strand":1,"description":"dihydropyrimidinase like 5 [Source:HGNC Symbol;Acc:HGNC:20637]"}, {"versioned_ensembl_gene_id":"ENSG00000168675.18","gene_symbol":"LDLRAD4","gene_name":"low density lipoprotein receptor class A domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1224]","synonyms":"C18orf1","biotype":"protein_coding","ncbi_id":"753","summary":null,"start":13217498,"end":13652755,"strand":1,"description":"low density lipoprotein receptor class A domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1224]"}, {"versioned_ensembl_gene_id":"ENSG00000215278.4","gene_symbol":"RPS7P6","gene_name":"ribosomal protein S7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270869","summary":null,"start":17427696,"end":17428274,"strand":-1,"description":"ribosomal protein S7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36334]"}, {"versioned_ensembl_gene_id":"ENSG00000254951.7","gene_symbol":"AC044810.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":7754393,"end":7905955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220598.1","gene_symbol":"SSR1P1","gene_name":"signal sequence receptor subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420476","summary":null,"start":150384307,"end":150385120,"strand":-1,"description":"signal sequence receptor subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39273]"}, {"versioned_ensembl_gene_id":"ENSG00000183303.2","gene_symbol":"OR5P2","gene_name":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]","synonyms":"JCG3","biotype":"protein_coding","ncbi_id":"120065","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7795905,"end":7796973,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]"}, {"versioned_ensembl_gene_id":"ENSG00000161921.14","gene_symbol":"CXCL16","gene_name":"C-X-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:16642]","synonyms":"SRPSOX,SR-PSOX,CXCLG16","biotype":"protein_coding","ncbi_id":"58191","summary":null,"start":4733526,"end":4739922,"strand":-1,"description":"C-X-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:16642]"}, {"versioned_ensembl_gene_id":"ENSG00000009765.14","gene_symbol":"IYD","gene_name":"iodotyrosine deiodinase [Source:HGNC Symbol;Acc:HGNC:21071]","synonyms":"dJ422F24.1,DEHAL1,C6orf71","biotype":"protein_coding","ncbi_id":"389434","summary":"This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":150368892,"end":150405969,"strand":1,"description":"iodotyrosine deiodinase [Source:HGNC Symbol;Acc:HGNC:21071]"}, {"versioned_ensembl_gene_id":"ENSG00000174473.15","gene_symbol":"GALNTL6","gene_name":"polypeptide N-acetylgalactosaminyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:33844]","synonyms":"GALNT17,GalNAc-T6L","biotype":"protein_coding","ncbi_id":"442117","summary":null,"start":171812254,"end":173041559,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:33844]"}, {"versioned_ensembl_gene_id":"ENSG00000261846.2","gene_symbol":"AADACL2","gene_name":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]","synonyms":"MGC72001","biotype":"protein_coding","ncbi_id":"344752","summary":null,"start":151744454,"end":151770036,"strand":1,"description":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]"}, {"versioned_ensembl_gene_id":"ENSG00000170688.4","gene_symbol":"OR5E1P","gene_name":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]","synonyms":"TPCR24,OR5E1,HSTPCR24","biotype":"unprocessed_pseudogene","ncbi_id":"26343","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7848700,"end":7849626,"strand":1,"description":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]"}, {"versioned_ensembl_gene_id":"ENSG00000241008.1","gene_symbol":"AC044810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7783697,"end":7784407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076716.8","gene_symbol":"GPC4","gene_name":"glypican 4 [Source:HGNC Symbol;Acc:HGNC:4452]","synonyms":"K-glypican","biotype":"protein_coding","ncbi_id":"2239","summary":"Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The GPC4 gene is adjacent to the 3' end of GPC3 and may also play a role in Simpson-Golabi-Behmel syndrome. [provided by RefSeq, Jul 2008]","start":133300103,"end":133415490,"strand":-1,"description":"glypican 4 [Source:HGNC Symbol;Acc:HGNC:4452]"}, {"versioned_ensembl_gene_id":"ENSG00000231453.1","gene_symbol":"LINC01305","gene_name":"long intergenic non-protein coding RNA 1305 [Source:HGNC Symbol;Acc:HGNC:27690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285084","summary":null,"start":174326027,"end":174330643,"strand":1,"description":"long intergenic non-protein coding RNA 1305 [Source:HGNC Symbol;Acc:HGNC:27690]"}, {"versioned_ensembl_gene_id":"ENSG00000272486.1","gene_symbol":"AC090922.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124579631,"end":124580648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226422.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31218662,"end":31222831,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000258853.1","gene_symbol":"AC021979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27684498,"end":27685768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227892.1","gene_symbol":"OR5P4P","gene_name":"olfactory receptor family 5 subfamily P member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15295]","synonyms":"OST730","biotype":"unprocessed_pseudogene","ncbi_id":"81185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7745990,"end":7746906,"strand":1,"description":"olfactory receptor family 5 subfamily P member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15295]"}, {"versioned_ensembl_gene_id":"ENSG00000227180.1","gene_symbol":"AC013467.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174299324,"end":174300956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137673.8","gene_symbol":"MMP7","gene_name":"matrix metallopeptidase 7 [Source:HGNC Symbol;Acc:HGNC:7174]","synonyms":"PUMP-1,MPSL1","biotype":"protein_coding","ncbi_id":"4316","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down proteoglycans, fibronectin, elastin and casein and differs from most MMP family members in that it lacks a conserved C-terminal hemopexin domain. The enzyme is involved in wound healing, and studies in mice suggest that it regulates the activity of defensins in intestinal mucosa. The gene is part of a cluster of MMP genes on chromosome 11. This gene exhibits elevated expression levels in multiple human cancers. [provided by RefSeq, Jan 2016]","start":102520508,"end":102530753,"strand":-1,"description":"matrix metallopeptidase 7 [Source:HGNC Symbol;Acc:HGNC:7174]"}, {"versioned_ensembl_gene_id":"ENSG00000275612.1","gene_symbol":"AC104237.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7698951,"end":7699393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229101.1","gene_symbol":"ELOCP20","gene_name":"elongin C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38156]","synonyms":"TCEB1P20","biotype":"unprocessed_pseudogene","ncbi_id":"100287778","summary":null,"start":115556826,"end":115557475,"strand":1,"description":"elongin C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38156]"}, {"versioned_ensembl_gene_id":"ENSG00000166408.4","gene_symbol":"OR5P1P","gene_name":"olfactory receptor family 5 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14779]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79283","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7772890,"end":7773814,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14779]"}, {"versioned_ensembl_gene_id":"ENSG00000275989.1","gene_symbol":"AL442128.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110952722,"end":110952811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176716.5","gene_symbol":"OR10AB1P","gene_name":"olfactory receptor family 10 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14804]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390091","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7726436,"end":7729684,"strand":1,"description":"olfactory receptor family 10 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14804]"}, {"versioned_ensembl_gene_id":"ENSG00000237804.1","gene_symbol":"HNRNPA1P39","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:48768]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402112","summary":null,"start":174310015,"end":174310974,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:48768]"}, {"versioned_ensembl_gene_id":"ENSG00000182334.2","gene_symbol":"OR5P3","gene_name":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]","synonyms":"JCG1","biotype":"protein_coding","ncbi_id":"120066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7824818,"end":7830840,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]"}, {"versioned_ensembl_gene_id":"ENSG00000262466.5","gene_symbol":"AADACL2-AS1","gene_name":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928142","summary":null,"start":151761981,"end":151765669,"strand":-1,"description":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]"}, {"versioned_ensembl_gene_id":"ENSG00000271758.2","gene_symbol":"AC044810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7704628,"end":7882947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235180.1","gene_symbol":"LINC00601","gene_name":"long intergenic non-protein coding RNA 601 [Source:HGNC Symbol;Acc:HGNC:43916]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101101772","summary":null,"start":126413869,"end":126421879,"strand":-1,"description":"long intergenic non-protein coding RNA 601 [Source:HGNC Symbol;Acc:HGNC:43916]"}, {"versioned_ensembl_gene_id":"ENSG00000226141.1","gene_symbol":"AC244107.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154654546,"end":154655325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255492.1","gene_symbol":"AC104383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11856490,"end":11856859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254707.1","gene_symbol":"AC104237.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7705288,"end":7709517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232679.1","gene_symbol":"LINC01705","gene_name":"long intergenic non-protein coding RNA 1705 [Source:HGNC Symbol;Acc:HGNC:52493]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985307","summary":null,"start":222041705,"end":222064763,"strand":-1,"description":"long intergenic non-protein coding RNA 1705 [Source:HGNC Symbol;Acc:HGNC:52493]"}, {"versioned_ensembl_gene_id":"ENSG00000234033.1","gene_symbol":"RAC1P8","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874398","summary":null,"start":61805150,"end":61805676,"strand":1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42005]"}, {"versioned_ensembl_gene_id":"ENSG00000261898.2","gene_symbol":"AC091153.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4731756,"end":4732371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170242.17","gene_symbol":"USP47","gene_name":"ubiquitin specific peptidase 47 [Source:HGNC Symbol;Acc:HGNC:20076]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55031","summary":null,"start":11841423,"end":11959323,"strand":1,"description":"ubiquitin specific peptidase 47 [Source:HGNC Symbol;Acc:HGNC:20076]"}, {"versioned_ensembl_gene_id":"ENSG00000183378.11","gene_symbol":"OVCH2","gene_name":"ovochymase 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:29970]","synonyms":"OVTN","biotype":"protein_coding","ncbi_id":"341277","summary":null,"start":7689438,"end":7706421,"strand":-1,"description":"ovochymase 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:29970]"}, {"versioned_ensembl_gene_id":"ENSG00000226210.3","gene_symbol":"AC215219.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14522,"end":32015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213252.3","gene_symbol":"AP001282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106826392,"end":106827890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183214.12","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31389818,"end":31406373,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000161920.9","gene_symbol":"MED11","gene_name":"mediator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:32687]","synonyms":"MGC88387,HSPC296","biotype":"protein_coding","ncbi_id":"400569","summary":"MED11 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008]","start":4731428,"end":4733610,"strand":1,"description":"mediator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:32687]"}, {"versioned_ensembl_gene_id":"ENSG00000111906.17","gene_symbol":"HDDC2","gene_name":"HD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21078]","synonyms":"dJ167O5.2,CGI-130,C6orf74","biotype":"protein_coding","ncbi_id":"51020","summary":null,"start":125219962,"end":125302078,"strand":-1,"description":"HD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21078]"}, {"versioned_ensembl_gene_id":"ENSG00000236230.1","gene_symbol":"AL356108.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222089169,"end":222387434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265148.5","gene_symbol":"TSPOAP1-AS1","gene_name":"TSPOAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44148]","synonyms":"BZRAP1-AS1","biotype":"antisense_RNA","ncbi_id":"100506779","summary":null,"start":58325450,"end":58415766,"strand":1,"description":"TSPOAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44148]"}, {"versioned_ensembl_gene_id":"ENSG00000227613.1","gene_symbol":"QRSL1P2","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43668]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422330","summary":null,"start":222261833,"end":222262796,"strand":-1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43668]"}, {"versioned_ensembl_gene_id":"ENSG00000270856.1","gene_symbol":"AL353765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61927090,"end":61927272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225760.2","gene_symbol":"LINC00431","gene_name":"long intergenic non-protein coding RNA 431 [Source:HGNC Symbol;Acc:HGNC:42766]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"104355135","summary":null,"start":110965704,"end":110990579,"strand":1,"description":"long intergenic non-protein coding RNA 431 [Source:HGNC Symbol;Acc:HGNC:42766]"}, {"versioned_ensembl_gene_id":"ENSG00000242654.1","gene_symbol":"RPL32P14","gene_name":"ribosomal protein L32 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37038]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270994","summary":null,"start":19041009,"end":19041386,"strand":1,"description":"ribosomal protein L32 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37038]"}, {"versioned_ensembl_gene_id":"ENSG00000251487.1","gene_symbol":"AC106744.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19035197,"end":19038799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226643.2","gene_symbol":"AL513314.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222452738,"end":222454705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266289.1","gene_symbol":"AC012213.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103383078,"end":103383854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228160.1","gene_symbol":"AL158069.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69569669,"end":69570357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229578.2","gene_symbol":"LINC00358","gene_name":"long intergenic non-protein coding RNA 358 [Source:HGNC Symbol;Acc:HGNC:42678]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874143","summary":null,"start":62003525,"end":62029548,"strand":-1,"description":"long intergenic non-protein coding RNA 358 [Source:HGNC Symbol;Acc:HGNC:42678]"}, {"versioned_ensembl_gene_id":"ENSG00000251000.1","gene_symbol":"AC008592.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95834424,"end":95835046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249174.1","gene_symbol":"AC106744.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18965861,"end":19142346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258186.2","gene_symbol":"SLC7A5P2","gene_name":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]","synonyms":"IMAA,hLAT1-3TM","biotype":"transcribed_processed_pseudogene","ncbi_id":"387254","summary":null,"start":21519830,"end":21520365,"strand":-1,"description":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]"}, {"versioned_ensembl_gene_id":"ENSG00000249557.2","gene_symbol":"HSPD1P15","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35130]","synonyms":"HSPD1-15P","biotype":"processed_pseudogene","ncbi_id":"646273","summary":null,"start":19233366,"end":19234487,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35130]"}, {"versioned_ensembl_gene_id":"ENSG00000234419.1","gene_symbol":"CICP13","gene_name":"capicua transcriptional repressor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37907]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728615","summary":null,"start":222468094,"end":222470882,"strand":1,"description":"capicua transcriptional repressor pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37907]"}, {"versioned_ensembl_gene_id":"ENSG00000249564.1","gene_symbol":"AC097510.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29907659,"end":29907791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180747.15","gene_symbol":"SMG1P3","gene_name":"SMG1P3, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49860]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100271836","summary":null,"start":21446683,"end":21520444,"strand":-1,"description":"SMG1P3, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49860]"}, {"versioned_ensembl_gene_id":"ENSG00000230142.2","gene_symbol":"LINC01075","gene_name":"long intergenic non-protein coding RNA 1075 [Source:HGNC Symbol;Acc:HGNC:49118]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103752583","summary":null,"start":62212577,"end":62249947,"strand":1,"description":"long intergenic non-protein coding RNA 1075 [Source:HGNC Symbol;Acc:HGNC:49118]"}, {"versioned_ensembl_gene_id":"ENSG00000271114.1","gene_symbol":"AL590392.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87891424,"end":87891869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219722.1","gene_symbol":"AL356057.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75499705,"end":75500136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244031.3","gene_symbol":"RPS3AP17","gene_name":"ribosomal protein S3a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36083]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271130","summary":null,"start":29962644,"end":29963758,"strand":-1,"description":"ribosomal protein S3a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36083]"}, {"versioned_ensembl_gene_id":"ENSG00000248637.1","gene_symbol":"AC108064.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172380028,"end":172380487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237619.1","gene_symbol":"OR3B1P","gene_name":"olfactory receptor family 3 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14839]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392561","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":154658790,"end":154659682,"strand":-1,"description":"olfactory receptor family 3 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14839]"}, {"versioned_ensembl_gene_id":"ENSG00000220730.2","gene_symbol":"AL356057.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75586122,"end":75586461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251409.1","gene_symbol":"AC008592.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95835943,"end":95852721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227611.1","gene_symbol":"LINC01074","gene_name":"long intergenic non-protein coding RNA 1074 [Source:HGNC Symbol;Acc:HGNC:49117]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144607","summary":null,"start":62321305,"end":62322398,"strand":1,"description":"long intergenic non-protein coding RNA 1074 [Source:HGNC Symbol;Acc:HGNC:49117]"}, {"versioned_ensembl_gene_id":"ENSG00000256480.1","gene_symbol":"AC018653.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7237432,"end":7240986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236882.7","gene_symbol":"LINC01554","gene_name":"long intergenic non-protein coding RNA 1554 [Source:HGNC Symbol;Acc:HGNC:24687]","synonyms":"FLJ38821,FIS,C5orf27","biotype":"lincRNA","ncbi_id":"202299","summary":null,"start":95852232,"end":95860133,"strand":1,"description":"long intergenic non-protein coding RNA 1554 [Source:HGNC Symbol;Acc:HGNC:24687]"}, {"versioned_ensembl_gene_id":"ENSG00000248281.1","gene_symbol":"AC106868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30006951,"end":30008316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276668.1","gene_symbol":"AC104237.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7699562,"end":7699988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006210.6","gene_symbol":"CX3CL1","gene_name":"C-X3-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10647]","synonyms":"SCYD1,NTN,neurotactin,fractalkine,CXC3C,CXC3,C3Xkine,ABCD-3","biotype":"protein_coding","ncbi_id":"6376","summary":"This gene belongs to the CX3C subgroup of chemokines, characterized by the number of amino acids located between the conserved cysteine residues. This is the only member of the CX3C subgroup, which contains three amino acids between cysteine residues, resulting in a Cys-X-X-X-Cys configuration. The encoded protein contains an extended mucin-like stalk with a chemokine domain on top, and exists in both a membrane-anchored form where it acts as a binding molecule, or, in soluble form, as a chemotactic cytokine. The mature form of this protein can be cleaved at the cell surface, yielding different soluble forms that can interact with the G-protein coupled receptor, C-X3-C motif chemokine receptor 1 gene product. This gene plays a role in a wide range of diseases, including cancer, vasculitis, neuropathies, atherosclerosis, inflammatory diseases, and in human immunodeficiency virus infections. [provided by RefSeq, Sep 2017]","start":57372458,"end":57385048,"strand":1,"description":"C-X3-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10647]"}, {"versioned_ensembl_gene_id":"ENSG00000229307.1","gene_symbol":"LINC00459","gene_name":"long intergenic non-protein coding RNA 459 [Source:HGNC Symbol;Acc:HGNC:42808]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874180","summary":null,"start":62323657,"end":62328833,"strand":1,"description":"long intergenic non-protein coding RNA 459 [Source:HGNC Symbol;Acc:HGNC:42808]"}, {"versioned_ensembl_gene_id":"ENSG00000215009.5","gene_symbol":"ACSM4","gene_name":"acyl-CoA synthetase medium chain family member 4 [Source:HGNC Symbol;Acc:HGNC:32016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341392","summary":null,"start":7304284,"end":7328724,"strand":1,"description":"acyl-CoA synthetase medium chain family member 4 [Source:HGNC Symbol;Acc:HGNC:32016]"}, {"versioned_ensembl_gene_id":"ENSG00000128596.16","gene_symbol":"CCDC136","gene_name":"coiled-coil domain containing 136 [Source:HGNC Symbol;Acc:HGNC:22225]","synonyms":"NAG6,KIAA1793,DKFZP434G156","biotype":"protein_coding","ncbi_id":"64753","summary":null,"start":128790757,"end":128822132,"strand":1,"description":"coiled-coil domain containing 136 [Source:HGNC Symbol;Acc:HGNC:22225]"}, {"versioned_ensembl_gene_id":"ENSG00000185274.11","gene_symbol":"GALNT17","gene_name":"polypeptide N-acetylgalactosaminyltransferase 17 [Source:HGNC Symbol;Acc:HGNC:16347]","synonyms":"GalNAc-T5L,GalNAc-T19,GalNAc-T17,WBSCR17,ppGalNAc-T17,GALNTL3","biotype":"protein_coding","ncbi_id":"64409","summary":"This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]","start":71132169,"end":71713600,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 17 [Source:HGNC Symbol;Acc:HGNC:16347]"}, {"versioned_ensembl_gene_id":"ENSG00000225870.1","gene_symbol":"LINC00368","gene_name":"long intergenic non-protein coding RNA 368 [Source:HGNC Symbol;Acc:HGNC:42690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927802","summary":null,"start":111095838,"end":111103097,"strand":1,"description":"long intergenic non-protein coding RNA 368 [Source:HGNC Symbol;Acc:HGNC:42690]"}, {"versioned_ensembl_gene_id":"ENSG00000232105.1","gene_symbol":"RPL32P28","gene_name":"ribosomal protein L32 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36328]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133193","summary":null,"start":62327988,"end":62328384,"strand":1,"description":"ribosomal protein L32 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36328]"}, {"versioned_ensembl_gene_id":"ENSG00000263513.5","gene_symbol":"FAM72C","gene_name":"family with sequence similarity 72 member C [Source:HGNC Symbol;Acc:HGNC:30602]","synonyms":"RP5-998N21.9","biotype":"protein_coding","ncbi_id":"554282","summary":null,"start":143955364,"end":143971965,"strand":-1,"description":"family with sequence similarity 72 member C [Source:HGNC Symbol;Acc:HGNC:30602]"}, {"versioned_ensembl_gene_id":"ENSG00000078053.16","gene_symbol":"AMPH","gene_name":"amphiphysin [Source:HGNC Symbol;Acc:HGNC:471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"273","summary":"This gene encodes a protein associated with the cytoplasmic surface of synaptic vesicles. A subset of patients with stiff-man syndrome who were also affected by breast cancer are positive for autoantibodies against this protein. Alternate splicing of this gene results in two transcript variants encoding different isoforms. Additional splice variants have been described, but their full length sequences have not been determined. A pseudogene of this gene is found on chromosome 11.[provided by RefSeq, Nov 2010]","start":38383704,"end":38631567,"strand":-1,"description":"amphiphysin [Source:HGNC Symbol;Acc:HGNC:471]"}, {"versioned_ensembl_gene_id":"ENSG00000272021.1","gene_symbol":"AC008592.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95849309,"end":95849855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242689.2","gene_symbol":"CNTF","gene_name":"ciliary neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:2169]","synonyms":"HCNTF","biotype":"protein_coding","ncbi_id":"1270","summary":"The protein encoded by this gene is a polypeptide hormone whose actions appear to be restricted to the nervous system where it promotes neurotransmitter synthesis and neurite outgrowth in certain neuronal populations. The protein is a potent survival factor for neurons and oligodendrocytes and may be relevant in reducing tissue destruction during inflammatory attacks. A mutation in this gene, which results in aberrant splicing, leads to ciliary neurotrophic factor deficiency, but this phenotype is not causally related to neurologic disease. A read-through transcript variant composed of the upstream ZFP91 gene and CNTF sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. [provided by RefSeq, Oct 2010]","start":58622673,"end":58625733,"strand":1,"description":"ciliary neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:2169]"}, {"versioned_ensembl_gene_id":"ENSG00000276149.1","gene_symbol":"BX005040.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":61202718,"end":61203087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176988.8","gene_symbol":"FMR1NB","gene_name":"FMR1 neighbor [Source:HGNC Symbol;Acc:HGNC:26372]","synonyms":"NY-SAR-35,FLJ25736,CT37","biotype":"protein_coding","ncbi_id":"158521","summary":null,"start":147981329,"end":148026667,"strand":1,"description":"FMR1 neighbor [Source:HGNC Symbol;Acc:HGNC:26372]"}, {"versioned_ensembl_gene_id":"ENSG00000276040.4","gene_symbol":"SPATA31A7","gene_name":"SPATA31 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:32007]","synonyms":"SPATA31A4,FAM75A7,FAM75A4","biotype":"protein_coding","ncbi_id":"26165","summary":null,"start":61190003,"end":61196280,"strand":1,"description":"SPATA31 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:32007]"}, {"versioned_ensembl_gene_id":"ENSG00000255545.7","gene_symbol":"AP004608.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":134436473,"end":134505661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269570.2","gene_symbol":"AP001350.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58611119,"end":58612642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255073.8","gene_symbol":"ZFP91-CNTF","gene_name":"ZFP91-CNTF readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"386607","summary":"This gene represents a read-through transcript composed of ZFP91 and CNTF sequence. This transcript is thought to be non-coding because it would be subject to nonsense-mediated mRNA decay (NMD). Read-through transcription of ZFP91 and CNTF has also been observed in mouse. [provided by RefSeq, Aug 2008]","start":58579172,"end":58624639,"strand":1,"description":"ZFP91-CNTF readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33441]"}, {"versioned_ensembl_gene_id":"ENSG00000154493.17","gene_symbol":"C10orf90","gene_name":"chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:26563]","synonyms":"FLJ32938,FATS,bA422P15.2","biotype":"protein_coding","ncbi_id":"118611","summary":null,"start":126424997,"end":126670446,"strand":-1,"description":"chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:26563]"}, {"versioned_ensembl_gene_id":"ENSG00000249406.1","gene_symbol":"AC015909.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50208972,"end":50214459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182793.11","gene_symbol":"GSTA5","gene_name":"glutathione S-transferase alpha 5 [Source:HGNC Symbol;Acc:HGNC:19662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"221357","summary":"The glutathione S-transferases (GST; EC 2.5.1.18) catalyze the conjugation of reduced glutathiones and a variety of electrophiles, including many known carcinogens and mutagens. The cytosolic GSTs belong to a large superfamily, with members located on different chromosomes. For additional information on GSTs, see GSTA1 (MIM 138359).[supplied by OMIM, Sep 2008]","start":52831655,"end":52846095,"strand":-1,"description":"glutathione S-transferase alpha 5 [Source:HGNC Symbol;Acc:HGNC:19662]"}, {"versioned_ensembl_gene_id":"ENSG00000263176.1","gene_symbol":"AC015909.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50212933,"end":50215357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236913.1","gene_symbol":"AC025750.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42469817,"end":42470266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223843.4","gene_symbol":"EFCAB6-AS1","gene_name":"EFCAB6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39999]","synonyms":"CITF22-123F2.1","biotype":"antisense_RNA","ncbi_id":"100874197","summary":null,"start":43516107,"end":43537117,"strand":1,"description":"EFCAB6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39999]"}, {"versioned_ensembl_gene_id":"ENSG00000256496.1","gene_symbol":"AC073913.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127317709,"end":127319986,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158488.15","gene_symbol":"CD1E","gene_name":"CD1e molecule [Source:HGNC Symbol;Acc:HGNC:1638]","synonyms":null,"biotype":"protein_coding","ncbi_id":"913","summary":"This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes within Golgi compartments, endosomes, and lysosomes, and is cleaved into a stable soluble form. The soluble form is required for the intracellular processing of some glycolipids into a form that can be presented by other CD1 family members. Many alternatively spliced transcript variants encoding different isoforms have been described. Additional transcript variants have been found; however, their biological validity has not been determined. [provided by RefSeq, Jun 2010]","start":158353696,"end":158357553,"strand":1,"description":"CD1e molecule [Source:HGNC Symbol;Acc:HGNC:1638]"}, {"versioned_ensembl_gene_id":"ENSG00000232526.1","gene_symbol":"VDAC1P13","gene_name":"voltage dependent anion channel 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420568","summary":null,"start":42463139,"end":42463997,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50515]"}, {"versioned_ensembl_gene_id":"ENSG00000251085.1","gene_symbol":"LINC01969","gene_name":"long intergenic non-protein coding RNA 1969 [Source:HGNC Symbol;Acc:HGNC:52795]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927230","summary":null,"start":50214694,"end":50215420,"strand":1,"description":"long intergenic non-protein coding RNA 1969 [Source:HGNC Symbol;Acc:HGNC:52795]"}, {"versioned_ensembl_gene_id":"ENSG00000254573.1","gene_symbol":"AP004550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134563396,"end":134573056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171126.7","gene_symbol":"KCNG3","gene_name":"potassium voltage-gated channel modifier subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:18306]","synonyms":"Kv6.3","biotype":"protein_coding","ncbi_id":"170850","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This member is a gamma subunit functioning as a modulatory molecule. Alternative splicing results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":42442017,"end":42494097,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:18306]"}, {"versioned_ensembl_gene_id":"ENSG00000274929.1","gene_symbol":"AL157813.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48532013,"end":48532599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249838.1","gene_symbol":"SUMO2P7","gene_name":"SUMO2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131823","summary":null,"start":50235845,"end":50236129,"strand":1,"description":"SUMO2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39017]"}, {"versioned_ensembl_gene_id":"ENSG00000254989.1","gene_symbol":"AP001999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134671426,"end":134672024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239300.5","gene_symbol":"AC080162.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9505445,"end":9512412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136161.12","gene_symbol":"RCBTB2","gene_name":"RCC1 and BTB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:1914]","synonyms":"CHC1L","biotype":"protein_coding","ncbi_id":"1102","summary":"This gene encodes a protein containing two C-terminal BTB/POZ domains that is related to regulator of chromosome condensation (RCC). The encoded protein may act as a guanine nucleotide exchange factor. This gene is observed to be lost or underexpressed in prostate cancers. There is a pseudogene of this gene on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":48488959,"end":48533256,"strand":-1,"description":"RCC1 and BTB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:1914]"}, {"versioned_ensembl_gene_id":"ENSG00000186660.14","gene_symbol":"ZFP91","gene_name":"ZFP91 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:14983]","synonyms":"ZNF757,PZF","biotype":"protein_coding","ncbi_id":"80829","summary":"The protein encoded by this gene is a member of the zinc finger family of proteins. The gene product contains C2H2-type domains, which are the classical zinc finger domains found in numerous nucleic acid-binding proteins. This protein functions as a regulator of the non-canonical NF-kappaB pathway in lymphotoxin-beta receptor signaling. Alternative splicing results in multiple transcript variants. A read-through transcript variant composed of ZFP91 and the downstream CNTF gene sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. A ZFP91-related pseudogene has also been identified on chromosome 2. [provided by RefSeq, Oct 2010]","start":58579111,"end":58621042,"strand":1,"description":"ZFP91 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:14983]"}, {"versioned_ensembl_gene_id":"ENSG00000255344.1","gene_symbol":"AP001999.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134714542,"end":134715922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251226.1","gene_symbol":"AP001999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134735596,"end":134763810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185988.12","gene_symbol":"PLK5","gene_name":"polo like kinase 5 [Source:HGNC Symbol;Acc:HGNC:27001]","synonyms":"SgK384ps,PLK5P","biotype":"protein_coding","ncbi_id":"126520","summary":null,"start":1524074,"end":1535456,"strand":1,"description":"polo like kinase 5 [Source:HGNC Symbol;Acc:HGNC:27001]"}, {"versioned_ensembl_gene_id":"ENSG00000151694.12","gene_symbol":"ADAM17","gene_name":"ADAM metallopeptidase domain 17 [Source:HGNC Symbol;Acc:HGNC:195]","synonyms":"CD156B,TACE,cSVP","biotype":"protein_coding","ncbi_id":"6868","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature protease. The encoded protease functions in the ectodomain shedding of tumor necrosis factor-alpha, in which soluble tumor necrosis factor-alpha is released from the membrane-bound precursor. This protease also functions in the processing of numerous other substrates, including cell adhesion proteins, cytokine and growth factor receptors and epidermal growth factor (EGF) receptor ligands, and plays a prominent role in the activation of the Notch signaling pathway. Elevated expression of this gene has been observed in specific cell types derived from psoriasis, rheumatoid arthritis, multiple sclerosis and Crohn's disease patients, suggesting that the encoded protein may play a role in autoimmune disease. Additionally, this protease may play a role in viral infection through its cleavage of ACE2, the cellular receptor for SARS-CoV and SARS-CoV-2. [provided by RefSeq, Aug 2020]","start":9488486,"end":9555792,"strand":-1,"description":"ADAM metallopeptidase domain 17 [Source:HGNC Symbol;Acc:HGNC:195]"}, {"versioned_ensembl_gene_id":"ENSG00000248546.3","gene_symbol":"ANP32C","gene_name":"acidic nuclear phosphoprotein 32 family member C [Source:HGNC Symbol;Acc:HGNC:16675]","synonyms":"PP32R1","biotype":"processed_pseudogene","ncbi_id":"23520","summary":null,"start":164197007,"end":164197711,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member C [Source:HGNC Symbol;Acc:HGNC:16675]"}, {"versioned_ensembl_gene_id":"ENSG00000250746.1","gene_symbol":"AC105250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164188311,"end":164190367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164934.13","gene_symbol":"DCAF13","gene_name":"DDB1 and CUL4 associated factor 13 [Source:HGNC Symbol;Acc:HGNC:24535]","synonyms":"Sof1,HSPC064,Gm83,DKFZP564O0463,WDSOF1","biotype":"protein_coding","ncbi_id":"25879","summary":null,"start":103414714,"end":103443453,"strand":1,"description":"DDB1 and CUL4 associated factor 13 [Source:HGNC Symbol;Acc:HGNC:24535]"}, {"versioned_ensembl_gene_id":"ENSG00000259078.2","gene_symbol":"PTBP1P","gene_name":"polypyrimidine tract binding protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:20030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122888","summary":null,"start":65279267,"end":65281166,"strand":1,"description":"polypyrimidine tract binding protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:20030]"}, {"versioned_ensembl_gene_id":"ENSG00000203688.4","gene_symbol":"LINC02487","gene_name":"long intergenic non-protein coding RNA 2487 [Source:HGNC Symbol;Acc:HGNC:53466]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441178","summary":null,"start":167679626,"end":167683787,"strand":-1,"description":"long intergenic non-protein coding RNA 2487 [Source:HGNC Symbol;Acc:HGNC:53466]"}, {"versioned_ensembl_gene_id":"ENSG00000169692.12","gene_symbol":"AGPAT2","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:325]","synonyms":"LPAAT-beta,BSCL","biotype":"protein_coding","ncbi_id":"10555","summary":"This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. The protein is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in this gene have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":136673143,"end":136687423,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:325]"}, {"versioned_ensembl_gene_id":"ENSG00000255726.1","gene_symbol":"AL662844.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31222913,"end":31223093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145416.13","gene_symbol":"MARCH1","gene_name":"membrane associated ring-CH-type finger 1 [Source:HGNC Symbol;Acc:HGNC:26077]","synonyms":"RNF171,MARCH-I,FLJ20668","biotype":"protein_coding","ncbi_id":"55016","summary":"MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010]","start":163524298,"end":164384050,"strand":-1,"description":"membrane associated ring-CH-type finger 1 [Source:HGNC Symbol;Acc:HGNC:26077]"}, {"versioned_ensembl_gene_id":"ENSG00000147684.7","gene_symbol":"NDUFB9","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 [Source:HGNC Symbol;Acc:HGNC:7704]","synonyms":"UQOR22,LYRM3,B22","biotype":"protein_coding","ncbi_id":"4715","summary":"The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":124539103,"end":124568510,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B9 [Source:HGNC Symbol;Acc:HGNC:7704]"}, {"versioned_ensembl_gene_id":"ENSG00000165879.8","gene_symbol":"FRAT1","gene_name":"FRAT1, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:3944]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10023","summary":"The protein encoded by this gene belongs to the GSK-3-binding protein family. The protein inhibits GSK-3-mediated phosphorylation of beta-catenin and positively regulates the Wnt signaling pathway. It may function in tumor progression and in lymphomagenesis. [provided by RefSeq, Oct 2008]","start":97319267,"end":97321915,"strand":1,"description":"FRAT1, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:3944]"}, {"versioned_ensembl_gene_id":"ENSG00000255899.1","gene_symbol":"AL662844.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31224342,"end":31225058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178372.7","gene_symbol":"CALML5","gene_name":"calmodulin like 5 [Source:HGNC Symbol;Acc:HGNC:18180]","synonyms":"CLSP","biotype":"protein_coding","ncbi_id":"51806","summary":"This gene encodes a novel calcium binding protein expressed in the epidermis and related to the calmodulin family of calcium binding proteins. Functional studies with recombinant protein demonstrate it does bind calcium and undergoes a conformational change when it does so. Abundant expression is detected only in reconstructed epidermis and is restricted to differentiating keratinocytes. In addition, it can associate with transglutaminase 3, shown to be a key enzyme in the terminal differentiation of keratinocytes. [provided by RefSeq, Jul 2008]","start":5498697,"end":5499555,"strand":-1,"description":"calmodulin like 5 [Source:HGNC Symbol;Acc:HGNC:18180]"}, {"versioned_ensembl_gene_id":"ENSG00000164508.4","gene_symbol":"HIST1H2AA","gene_name":"histone cluster 1 H2A family member a [Source:HGNC Symbol;Acc:HGNC:18729]","synonyms":"bA317E16.2,H2AFR","biotype":"protein_coding","ncbi_id":"221613","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":25726132,"end":25726527,"strand":-1,"description":"histone cluster 1 H2A family member a [Source:HGNC Symbol;Acc:HGNC:18729]"}, {"versioned_ensembl_gene_id":"ENSG00000206403.11","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"BAT5,NG26,D6S82E","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31677180,"end":31693655,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000250472.1","gene_symbol":"TRIM36-IT1","gene_name":"TRIM36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41422]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874338","summary":null,"start":115148764,"end":115149644,"strand":-1,"description":"TRIM36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41422]"}, {"versioned_ensembl_gene_id":"ENSG00000075073.14","gene_symbol":"TACR2","gene_name":"tachykinin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11527]","synonyms":"TAC2R,SKR,NKNAR,NK2R","biotype":"protein_coding","ncbi_id":"6865","summary":"This gene belongs to a family of genes that function as receptors for tachykinins. Receptor affinities are specified by variations in the 5'-end of the sequence. The receptors belonging to this family are characterized by interactions with G proteins and 7 hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin neuropeptide substance K, also referred to as neurokinin A. [provided by RefSeq, Jul 2008]","start":69403903,"end":69416867,"strand":-1,"description":"tachykinin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11527]"}, {"versioned_ensembl_gene_id":"ENSG00000164933.11","gene_symbol":"SLC25A32","gene_name":"solute carrier family 25 member 32 [Source:HGNC Symbol;Acc:HGNC:29683]","synonyms":"MFTC","biotype":"protein_coding","ncbi_id":"81034","summary":"This gene encodes a member of the P(I/L)W subfamily of mitochondrial carrier family transport proteins. The encoded protein transports folate across the inner mitochondrial membrane. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2013]","start":103398635,"end":103415189,"strand":-1,"description":"solute carrier family 25 member 32 [Source:HGNC Symbol;Acc:HGNC:29683]"}, {"versioned_ensembl_gene_id":"ENSG00000267702.1","gene_symbol":"AP005131.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":13486462,"end":13490676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178363.4","gene_symbol":"CALML3","gene_name":"calmodulin like 3 [Source:HGNC Symbol;Acc:HGNC:1452]","synonyms":"CLP","biotype":"protein_coding","ncbi_id":"810","summary":null,"start":5524009,"end":5526771,"strand":1,"description":"calmodulin like 3 [Source:HGNC Symbol;Acc:HGNC:1452]"}, {"versioned_ensembl_gene_id":"ENSG00000179832.17","gene_symbol":"MROH1","gene_name":"maestro heat like repeat family member 1 [Source:HGNC Symbol;Acc:HGNC:26958]","synonyms":"KIAA1833,HEATR7A","biotype":"protein_coding","ncbi_id":"727957","summary":null,"start":144148016,"end":144261940,"strand":1,"description":"maestro heat like repeat family member 1 [Source:HGNC Symbol;Acc:HGNC:26958]"}, {"versioned_ensembl_gene_id":"ENSG00000267529.3","gene_symbol":"AP005131.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":13471012,"end":13472709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267503.1","gene_symbol":"AP005131.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13561399,"end":13565035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170248.13","gene_symbol":"PDCD6IP","gene_name":"programmed cell death 6 interacting protein [Source:HGNC Symbol;Acc:HGNC:8766]","synonyms":"Hp95,Alix,AIP1","biotype":"protein_coding","ncbi_id":"10015","summary":"This gene encodes a protein that functions within the ESCRT pathway in the abscission stage of cytokinesis, in intralumenal endosomal vesicle formation, and in enveloped virus budding. Studies using mouse cells have shown that overexpression of this protein can block apoptosis. In addition, the product of this gene binds to the product of the PDCD6 gene, a protein required for apoptosis, in a calcium-dependent manner. This gene product also binds to endophilins, proteins that regulate membrane shape during endocytosis. Overexpression of this gene product and endophilins results in cytoplasmic vacuolization, which may be partly responsible for the protection against cell death. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. Related pseudogenes have been identified on chromosome 15. [provided by RefSeq, Jan 2012]","start":33798352,"end":33869707,"strand":1,"description":"programmed cell death 6 interacting protein [Source:HGNC Symbol;Acc:HGNC:8766]"}, {"versioned_ensembl_gene_id":"ENSG00000121481.10","gene_symbol":"RNF2","gene_name":"ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:10061]","synonyms":"DING,BAP1,BAP-1,RING2,RING1B,HIPI3","biotype":"protein_coding","ncbi_id":"6045","summary":"Polycomb group (PcG) of proteins form the multiprotein complexes that are important for the transcription repression of various genes involved in development and cell proliferation. The protein encoded by this gene is one of the PcG proteins. It has been shown to interact with, and suppress the activity of, transcription factor CP2 (TFCP2/CP2). Studies of the mouse counterpart suggested the involvement of this gene in the specification of anterior-posterior axis, as well as in cell proliferation in early development. This protein was also found to interact with huntingtin interacting protein 2 (HIP2), an ubiquitin-conjugating enzyme, and possess ubiquitin ligase activity. [provided by RefSeq, Jul 2008]","start":185045364,"end":185102608,"strand":1,"description":"ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:10061]"}, {"versioned_ensembl_gene_id":"ENSG00000132669.12","gene_symbol":"RIN2","gene_name":"Ras and Rab interactor 2 [Source:HGNC Symbol;Acc:HGNC:18750]","synonyms":"RASSF4","biotype":"protein_coding","ncbi_id":"54453","summary":"The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011]","start":19886521,"end":20002457,"strand":1,"description":"Ras and Rab interactor 2 [Source:HGNC Symbol;Acc:HGNC:18750]"}, {"versioned_ensembl_gene_id":"ENSG00000267694.1","gene_symbol":"AP005131.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13461020,"end":13470823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256462.1","gene_symbol":"AL732437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5524976,"end":5525742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255002.1","gene_symbol":"LINC02324","gene_name":"long intergenic non-protein coding RNA 2324 [Source:HGNC Symbol;Acc:HGNC:53244]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128233","summary":null,"start":65212893,"end":65222347,"strand":-1,"description":"long intergenic non-protein coding RNA 2324 [Source:HGNC Symbol;Acc:HGNC:53244]"}, {"versioned_ensembl_gene_id":"ENSG00000205488.8","gene_symbol":"CALML3-AS1","gene_name":"CALML3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44682]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132159","summary":null,"start":5514244,"end":5526246,"strand":-1,"description":"CALML3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44682]"}, {"versioned_ensembl_gene_id":"ENSG00000118434.8","gene_symbol":"SPACA1","gene_name":"sperm acrosome associated 1 [Source:HGNC Symbol;Acc:HGNC:14967]","synonyms":"SAMP32","biotype":"protein_coding","ncbi_id":"81833","summary":"The correlation of anti-sperm antibodies with cases of unexplained infertility implicates a role for these antibodies in blocking fertilization. Improved diagnosis and treatment of immunologic infertility, as well as identification of proteins for targeted contraception, are dependent on the identification and characterization of relevant sperm antigens. The protein expressed by this gene is recognized by anti-sperm antibodies from infertile males. Furthermore, antibodies generated against the recombinant protein block in vitro fertilization. This protein localizes to the acrosomal membrane of spermatids and mature spermatozoa where it is thought to play a role in acrosomal morphogenesis and in sperm-egg binding and fusion, respectively. [provided by RefSeq, Jul 2008]","start":88047789,"end":88066832,"strand":1,"description":"sperm acrosome associated 1 [Source:HGNC Symbol;Acc:HGNC:14967]"}, {"versioned_ensembl_gene_id":"ENSG00000226217.1","gene_symbol":"RPL19P1","gene_name":"ribosomal protein L19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16595]","synonyms":"dJ860F19.2","biotype":"processed_pseudogene","ncbi_id":"140759","summary":null,"start":2780614,"end":2781041,"strand":1,"description":"ribosomal protein L19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16595]"}, {"versioned_ensembl_gene_id":"ENSG00000267690.1","gene_symbol":"LDLRAD4-AS1","gene_name":"LDLRAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48592]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288122","summary":null,"start":13419421,"end":13427480,"strand":-1,"description":"LDLRAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48592]"}, {"versioned_ensembl_gene_id":"ENSG00000277412.1","gene_symbol":"BX005040.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61194211,"end":61203446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229759.1","gene_symbol":"MRPS18AP1","gene_name":"mitochondrial ribosomal protein S18A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359761","summary":null,"start":48256350,"end":48256938,"strand":-1,"description":"mitochondrial ribosomal protein S18A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29740]"}, {"versioned_ensembl_gene_id":"ENSG00000203690.11","gene_symbol":"TCP10","gene_name":"t-complex 10 [Source:HGNC Symbol;Acc:HGNC:11656]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6953","summary":null,"start":167357031,"end":167384510,"strand":-1,"description":"t-complex 10 [Source:HGNC Symbol;Acc:HGNC:11656]"}, {"versioned_ensembl_gene_id":"ENSG00000267177.1","gene_symbol":"AP002505.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13234945,"end":13236470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276997.4","gene_symbol":"AL513314.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222477252,"end":222504622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170807.11","gene_symbol":"LMOD2","gene_name":"leiomodin 2 [Source:HGNC Symbol;Acc:HGNC:6648]","synonyms":null,"biotype":"protein_coding","ncbi_id":"442721","summary":null,"start":123655807,"end":123664290,"strand":1,"description":"leiomodin 2 [Source:HGNC Symbol;Acc:HGNC:6648]"}, {"versioned_ensembl_gene_id":"ENSG00000204718.3","gene_symbol":"CNN2P12","gene_name":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131550","summary":null,"start":18726706,"end":18727414,"strand":1,"description":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]"}, {"versioned_ensembl_gene_id":"ENSG00000279275.1","gene_symbol":"AP002505.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":13279415,"end":13280110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266954.1","gene_symbol":"AP001010.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13644815,"end":13645685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267366.1","gene_symbol":"AP005131.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13500641,"end":13501289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267136.1","gene_symbol":"AP005131.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13514520,"end":13522888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232185.1","gene_symbol":"CNOT7P2","gene_name":"CCR4-NOT transcription complex subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132332","summary":null,"start":115564601,"end":115565432,"strand":1,"description":"CCR4-NOT transcription complex subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44249]"}, {"versioned_ensembl_gene_id":"ENSG00000258878.1","gene_symbol":"AL355076.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65234515,"end":65235101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175513.9","gene_symbol":"TSGA10IP","gene_name":"testis specific 10 interacting protein [Source:HGNC Symbol;Acc:HGNC:26555]","synonyms":"FLJ32880,FAM161C","biotype":"protein_coding","ncbi_id":"254187","summary":null,"start":65945445,"end":65959963,"strand":1,"description":"testis specific 10 interacting protein [Source:HGNC Symbol;Acc:HGNC:26555]"}, {"versioned_ensembl_gene_id":"ENSG00000213347.10","gene_symbol":"MXD3","gene_name":"MAX dimerization protein 3 [Source:HGNC Symbol;Acc:HGNC:14008]","synonyms":"MAD3,bHLHc13","biotype":"protein_coding","ncbi_id":"83463","summary":"This gene encodes a member of the Myc superfamily of basic helix-loop-helix leucine zipper transcriptional regulators. The encoded protein forms a heterodimer with the cofactor MAX which binds specific E-box DNA motifs in the promoters of target genes and regulates their transcription. Disruption of the MAX-MXD3 complex is associated with uncontrolled cell proliferation and tumorigenesis. Transcript variants of this gene encoding different isoforms have been described.[provided by RefSeq, Dec 2008]","start":177301461,"end":177312757,"strand":-1,"description":"MAX dimerization protein 3 [Source:HGNC Symbol;Acc:HGNC:14008]"}, {"versioned_ensembl_gene_id":"ENSG00000236898.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33232201,"end":33237743,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000180150.5","gene_symbol":"HMGN2P9","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:4987]","synonyms":"HMGN2L9,HMG17L1,dJ388M5.2","biotype":"processed_pseudogene","ncbi_id":"23605","summary":null,"start":43802544,"end":43802772,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:4987]"}, {"versioned_ensembl_gene_id":"ENSG00000273153.1","gene_symbol":"AC067747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17137336,"end":17137585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258760.1","gene_symbol":"AL355076.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65236480,"end":65318790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170873.18","gene_symbol":"MTSS1","gene_name":"MTSS1, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:20443]","synonyms":"MIM,KIAA0429,MIMB,MIMA","biotype":"protein_coding","ncbi_id":"9788","summary":null,"start":124550790,"end":124728429,"strand":-1,"description":"MTSS1, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:20443]"}, {"versioned_ensembl_gene_id":"ENSG00000270631.1","gene_symbol":"AL592436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115577229,"end":115577786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235500.2","gene_symbol":"SNX19P2","gene_name":"sorting nexin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38115]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400094","summary":null,"start":18892260,"end":18895230,"strand":-1,"description":"sorting nexin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38115]"}, {"versioned_ensembl_gene_id":"ENSG00000102970.10","gene_symbol":"CCL17","gene_name":"C-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:10615]","synonyms":"TARC,SCYA17,ABCD-2","biotype":"protein_coding","ncbi_id":"6361","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 16. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for T lymphocytes, but not monocytes or granulocytes. The product of this gene binds to chemokine receptors CCR4 and CCR8. This chemokine plays important roles in T cell development in thymus as well as in trafficking and activation of mature T cells. [provided by RefSeq, Sep 2014]","start":57404767,"end":57416062,"strand":1,"description":"C-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:10615]"}, {"versioned_ensembl_gene_id":"ENSG00000214759.3","gene_symbol":"AL355076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65268829,"end":65269098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258613.1","gene_symbol":"RPL21P7","gene_name":"ribosomal protein L21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"145370","summary":null,"start":65266638,"end":65267690,"strand":-1,"description":"ribosomal protein L21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19772]"}, {"versioned_ensembl_gene_id":"ENSG00000280414.1","gene_symbol":"AC018470.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":174334438,"end":174337566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217236.1","gene_symbol":"SP9","gene_name":"Sp9 transcription factor [Source:HGNC Symbol;Acc:HGNC:30690]","synonyms":"ZNF990","biotype":"protein_coding","ncbi_id":"100131390","summary":null,"start":174334946,"end":174338492,"strand":1,"description":"Sp9 transcription factor [Source:HGNC Symbol;Acc:HGNC:30690]"}, {"versioned_ensembl_gene_id":"ENSG00000178556.8","gene_symbol":"CKS1BP6","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652904","summary":null,"start":30617454,"end":30617693,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24608]"}, {"versioned_ensembl_gene_id":"ENSG00000106299.7","gene_symbol":"WASL","gene_name":"Wiskott-Aldrich syndrome like [Source:HGNC Symbol;Acc:HGNC:12735]","synonyms":"WASPB,NWASP,N-WASP","biotype":"protein_coding","ncbi_id":"8976","summary":"This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013]","start":123681935,"end":123749067,"strand":-1,"description":"Wiskott-Aldrich syndrome like [Source:HGNC Symbol;Acc:HGNC:12735]"}, {"versioned_ensembl_gene_id":"ENSG00000267305.2","gene_symbol":"AL592148.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":222510169,"end":222519732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280629.1","gene_symbol":"AC233280.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232368.1","gene_symbol":"FTLP2","gene_name":"ferritin light chain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4001]","synonyms":"FTLL2","biotype":"processed_pseudogene","ncbi_id":"392437","summary":null,"start":30630298,"end":30630825,"strand":1,"description":"ferritin light chain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4001]"}, {"versioned_ensembl_gene_id":"ENSG00000225809.1","gene_symbol":"RBMY2KP","gene_name":"RNA binding motif protein, Y-linked, family 2, member K pseudogene [Source:HGNC Symbol;Acc:HGNC:23888]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"140100","summary":null,"start":8264449,"end":8277188,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member K pseudogene [Source:HGNC Symbol;Acc:HGNC:23888]"}, {"versioned_ensembl_gene_id":"ENSG00000281798.1","gene_symbol":"AC233280.16","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226513.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33244216,"end":33247752,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000250362.1","gene_symbol":"AC008592.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":95861786,"end":95874519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197635.9","gene_symbol":"DPP4","gene_name":"dipeptidyl peptidase 4 [Source:HGNC Symbol;Acc:HGNC:3009]","synonyms":"DPPIV,CD26,ADCP2","biotype":"protein_coding","ncbi_id":"1803","summary":"The DPP4 gene encodes dipeptidyl peptidase 4, which is identical to adenosine deaminase complexing protein-2, and to the T-cell activation antigen CD26. It is an intrinsic type II transmembrane glycoprotein and a serine exopeptidase that cleaves X-proline dipeptides from the N-terminus of polypeptides. Dipeptidyl peptidase 4 is highly involved in glucose and insulin metabolism, as well as in immune regulation. This protein was shown to be a functional receptor for Middle East respiratory syndrome coronavirus (MERS-CoV), and protein modeling suggests that it may play a similar role with SARS-CoV-2, the virus responsible for COVID-19. [provided by RefSeq, Apr 2020]","start":161992241,"end":162074542,"strand":-1,"description":"dipeptidyl peptidase 4 [Source:HGNC Symbol;Acc:HGNC:3009]"}, {"versioned_ensembl_gene_id":"ENSG00000236195.1","gene_symbol":"RNMTL1P2","gene_name":"RNA methyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44906]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420223","summary":null,"start":17962079,"end":17963029,"strand":1,"description":"RNA methyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44906]"}, {"versioned_ensembl_gene_id":"ENSG00000272927.1","gene_symbol":"AC107464.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":661209,"end":661945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162746.14","gene_symbol":"FCRLB","gene_name":"Fc receptor like B [Source:HGNC Symbol;Acc:HGNC:26431]","synonyms":"FREB-2,FLJ31052,FCRLY,FCRLM2,FCRL2","biotype":"protein_coding","ncbi_id":"127943","summary":"FCRL2 belongs to the Fc receptor family. Fc receptors are involved in phagocytosis, antibody-dependent cell cytotoxicity, immediate hypersensitivity, and transcytosis of immunoglobulins via their ability to bind immunoglobulin (Ig) constant regions (Chikaev et al., 2005 [PubMed 15676285]).[supplied by OMIM, Mar 2008]","start":161721563,"end":161728143,"strand":1,"description":"Fc receptor like B [Source:HGNC Symbol;Acc:HGNC:26431]"}, {"versioned_ensembl_gene_id":"ENSG00000280340.1","gene_symbol":"AC080080.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18000290,"end":18000879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100142.14","gene_symbol":"POLR2F","gene_name":"RNA polymerase II subunit F [Source:HGNC Symbol;Acc:HGNC:9193]","synonyms":"RPB6,HRBP14.4","biotype":"protein_coding","ncbi_id":"5435","summary":"This gene encodes the sixth largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. In yeast, this polymerase subunit, in combination with at least two other subunits, forms a structure that stabilizes the transcribing polymerase on the DNA template. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":37952607,"end":38041915,"strand":1,"description":"RNA polymerase II subunit F [Source:HGNC Symbol;Acc:HGNC:9193]"}, {"versioned_ensembl_gene_id":"ENSG00000236905.2","gene_symbol":"AC104333.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212824027,"end":212824505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281160.1","gene_symbol":"AC018358.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42264989,"end":42266390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168379.8","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33252873,"end":33269193,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000281246.1","gene_symbol":"AF186996.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125703375,"end":125704277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229716.2","gene_symbol":"RPL23AP19","gene_name":"ribosomal protein L23a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131143","summary":null,"start":8831007,"end":8831375,"strand":1,"description":"ribosomal protein L23a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36708]"}, {"versioned_ensembl_gene_id":"ENSG00000133256.12","gene_symbol":"PDE6B","gene_name":"phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]","synonyms":"rd1,PDEB,CSNBAD2,CSNB3,RP40","biotype":"protein_coding","ncbi_id":"5158","summary":"Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":625584,"end":670782,"strand":1,"description":"phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]"}, {"versioned_ensembl_gene_id":"ENSG00000139874.5","gene_symbol":"SSTR1","gene_name":"somatostatin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11330]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6751","summary":"Somatostatins are peptide hormones that regulate diverse cellular functions such as neurotransmission, cell proliferation, and endocrine signaling as well as inhibiting the release of many hormones and other secretory proteins. Somatostatin has two active forms of 14 and 28 amino acids. The biological effects of somatostatins are mediated by a family of G-protein coupled somatostatin receptors that are expressed in a tissue-specific manner. The protein encoded by this gene is a member of the superfamily of somatostatin receptors having seven transmembrane segments. Somatostatin receptors form homodimers and heterodimers with other members of the superfamily as well as with other G-protein coupled receptors and receptor tyrosine kinases. This somatostatin receptor has greater affinity for somatostatin-14 than -28. [provided by RefSeq, Jul 2012]","start":38207999,"end":38213067,"strand":1,"description":"somatostatin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11330]"}, {"versioned_ensembl_gene_id":"ENSG00000273381.1","gene_symbol":"AL158071.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91206175,"end":91210299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173218.14","gene_symbol":"VANGL1","gene_name":"VANGL planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:15512]","synonyms":"STB2","biotype":"protein_coding","ncbi_id":"81839","summary":"This gene encodes a member of the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":115641953,"end":115698224,"strand":1,"description":"VANGL planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:15512]"}, {"versioned_ensembl_gene_id":"ENSG00000273449.1","gene_symbol":"AC093788.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163529771,"end":163530697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229937.6","gene_symbol":"PRPS1L1","gene_name":"phosphoribosyl pyrophosphate synthetase 1-like 1 [Source:HGNC Symbol;Acc:HGNC:9463]","synonyms":"PRPSL,PRPS3","biotype":"protein_coding","ncbi_id":"221823","summary":"This intronless gene is specifically expressed in the testis, and encodes a protein that is highly homologous to the two subunits of phosphoribosylpyrophosphate synthetase encoded by human X-linked genes, PRPS1 and PRPS2. These enzymes convert pyrimidine, purine or pyridine bases to the corresponding ribonucleoside monophosphates. In vitro transcription/translation and site-directed mutagenesis studies indicate that translation of this mRNA initiates exclusively at a non-AUG (ACG) codon. [provided by RefSeq, Jul 2008]","start":18026774,"end":18027863,"strand":-1,"description":"phosphoribosyl pyrophosphate synthetase 1-like 1 [Source:HGNC Symbol;Acc:HGNC:9463]"}, {"versioned_ensembl_gene_id":"ENSG00000177803.7","gene_symbol":"AC112247.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163932526,"end":163933182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185523.6","gene_symbol":"SPATA45","gene_name":"spermatogenesis associated 45 [Source:HGNC Symbol;Acc:HGNC:33709]","synonyms":"LOC149643,C1orf227","biotype":"protein_coding","ncbi_id":"149643","summary":null,"start":212830141,"end":212847649,"strand":-1,"description":"spermatogenesis associated 45 [Source:HGNC Symbol;Acc:HGNC:33709]"}, {"versioned_ensembl_gene_id":"ENSG00000232734.1","gene_symbol":"ATP5G1P7","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39510]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130962","summary":null,"start":69432972,"end":69433371,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39510]"}, {"versioned_ensembl_gene_id":"ENSG00000282327.1","gene_symbol":"AC134503.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180201159,"end":180201212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280982.1","gene_symbol":"AF186996.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125712140,"end":125713051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213158.6","gene_symbol":"GAPDHP36","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37790]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647249","summary":null,"start":180212191,"end":180213108,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37790]"}, {"versioned_ensembl_gene_id":"ENSG00000281785.1","gene_symbol":"AF186996.14","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125724567,"end":125725463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272686.1","gene_symbol":"AC006333.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123749068,"end":123751166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134330.18","gene_symbol":"IAH1","gene_name":"isoamyl acetate-hydrolyzing esterase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285148","summary":null,"start":9473658,"end":9496543,"strand":1,"description":"isoamyl acetate-hydrolyzing esterase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27696]"}, {"versioned_ensembl_gene_id":"ENSG00000232792.2","gene_symbol":"FTH1P25","gene_name":"ferritin heavy chain 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37643]","synonyms":"FTHL25","biotype":"processed_pseudogene","ncbi_id":"100462799","summary":null,"start":185071567,"end":185072035,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37643]"}, {"versioned_ensembl_gene_id":"ENSG00000230375.1","gene_symbol":"GSTA11P","gene_name":"glutathione S-transferase alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:49905]","synonyms":"GSTAP3","biotype":"unprocessed_pseudogene","ncbi_id":"647175","summary":null,"start":52847910,"end":52870329,"strand":-1,"description":"glutathione S-transferase alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:49905]"}, {"versioned_ensembl_gene_id":"ENSG00000236317.1","gene_symbol":"AC104333.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212855175,"end":212855366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239880.1","gene_symbol":"AC068760.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180323107,"end":180325059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227107.1","gene_symbol":"AC104667.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237612977,"end":237626525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198468.7","gene_symbol":"FLVCR1-AS1","gene_name":"FLVCR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39077]","synonyms":"NCRNA00292,LQK1","biotype":"lincRNA","ncbi_id":"642946","summary":null,"start":212852108,"end":212858088,"strand":-1,"description":"FLVCR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39077]"}, {"versioned_ensembl_gene_id":"ENSG00000255867.1","gene_symbol":"DENND5B-AS1","gene_name":"DENND5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42517]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874249","summary":null,"start":31589923,"end":31615666,"strand":1,"description":"DENND5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42517]"}, {"versioned_ensembl_gene_id":"ENSG00000241696.1","gene_symbol":"LINC02053","gene_name":"long intergenic non-protein coding RNA 2053 [Source:HGNC Symbol;Acc:HGNC:52893]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505609","summary":null,"start":180414174,"end":180422506,"strand":1,"description":"long intergenic non-protein coding RNA 2053 [Source:HGNC Symbol;Acc:HGNC:52893]"}, {"versioned_ensembl_gene_id":"ENSG00000275769.1","gene_symbol":"AC068792.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31443792,"end":31444208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120440.13","gene_symbol":"TTLL2","gene_name":"tubulin tyrosine ligase like 2 [Source:HGNC Symbol;Acc:HGNC:21211]","synonyms":"NYD-TSPG,dJ366N23.3,C6orf104","biotype":"protein_coding","ncbi_id":"83887","summary":null,"start":167325086,"end":167359503,"strand":1,"description":"tubulin tyrosine ligase like 2 [Source:HGNC Symbol;Acc:HGNC:21211]"}, {"versioned_ensembl_gene_id":"ENSG00000235182.1","gene_symbol":"AC104333.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212853280,"end":212853426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263749.1","gene_symbol":"OOSP1P2","gene_name":"oocyte secreted protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49241]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480252","summary":null,"start":32343774,"end":32344124,"strand":-1,"description":"oocyte secreted protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49241]"}, {"versioned_ensembl_gene_id":"ENSG00000105609.16","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR8,LIR-8,CD85c","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54249431,"end":54257301,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000225349.2","gene_symbol":"AC022080.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31534715,"end":31535247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225850.3","gene_symbol":"AL355490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97334564,"end":97343203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088882.7","gene_symbol":"CPXM1","gene_name":"carboxypeptidase X, M14 family member 1 [Source:HGNC Symbol;Acc:HGNC:15771]","synonyms":"CPXM,CPX1,CPX-1","biotype":"protein_coding","ncbi_id":"56265","summary":"This gene likely encodes a member of the carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a carboxypeptidase domain, but the protein appears to lack residues necessary for carboxypeptidase activity.[provided by RefSeq, May 2010]","start":2794069,"end":2800637,"strand":-1,"description":"carboxypeptidase X, M14 family member 1 [Source:HGNC Symbol;Acc:HGNC:15771]"}, {"versioned_ensembl_gene_id":"ENSG00000152128.13","gene_symbol":"TMEM163","gene_name":"transmembrane protein 163 [Source:HGNC Symbol;Acc:HGNC:25380]","synonyms":"SV31,DKFZP566N034","biotype":"protein_coding","ncbi_id":"81615","summary":null,"start":134455759,"end":134719000,"strand":-1,"description":"transmembrane protein 163 [Source:HGNC Symbol;Acc:HGNC:25380]"}, {"versioned_ensembl_gene_id":"ENSG00000241946.1","gene_symbol":"AC068298.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180589887,"end":180590047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181274.6","gene_symbol":"FRAT2","gene_name":"FRAT2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:16048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23401","summary":"The protein encoded by this intronless gene belongs to the GSK-3-binding protein family. Studies show that this protein plays a role as a positive regulator of the WNT signaling pathway. It may be upregulated in tumor progression. [provided by RefSeq, Jul 2008]","start":97332497,"end":97334709,"strand":-1,"description":"FRAT2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:16048]"}, {"versioned_ensembl_gene_id":"ENSG00000170456.15","gene_symbol":"DENND5B","gene_name":"DENN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:28338]","synonyms":"MGC24039","biotype":"protein_coding","ncbi_id":"160518","summary":null,"start":31382223,"end":31591097,"strand":-1,"description":"DENN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:28338]"}, {"versioned_ensembl_gene_id":"ENSG00000239774.1","gene_symbol":"AC125618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180566718,"end":180601935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213606.3","gene_symbol":"AKR1B10P1","gene_name":"aldo-keto reductase family 1 member B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340888","summary":null,"start":67750284,"end":67751225,"strand":1,"description":"aldo-keto reductase family 1 member B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45062]"}, {"versioned_ensembl_gene_id":"ENSG00000148090.11","gene_symbol":"AUH","gene_name":"AU RNA binding methylglutaconyl-CoA hydratase [Source:HGNC Symbol;Acc:HGNC:890]","synonyms":null,"biotype":"protein_coding","ncbi_id":"549","summary":"This gene encodes bifunctional mitochondrial protein that has both RNA-binding and hydratase activities. The encoded protein is a methylglutaconyl-CoA hydratase that catalyzes the hydration of 3-methylglutaconyl-CoA to 3-hydroxy-3-methyl-glutaryl-CoA, a critical step in the leucine degradation pathway. This protein also binds AU-rich elements (AREs) found in the 3' UTRs of rapidly decaying mRNAs including c-fos, c-myc and granulocyte/ macrophage colony stimulating factor. ARE elements are involved in directing RNA to rapid degradation and deadenylation. This protein is localizes to the mitochondrial matrix and the inner mitochondrial membrane and may be involved in mitochondrial protein synthesis. Mutations in this gene are the cause of 3-methylglutaconic aciduria, type I. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":91213815,"end":91361913,"strand":-1,"description":"AU RNA binding methylglutaconyl-CoA hydratase [Source:HGNC Symbol;Acc:HGNC:890]"}, {"versioned_ensembl_gene_id":"ENSG00000263745.6","gene_symbol":"AP005230.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1883524,"end":2489426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217447.1","gene_symbol":"AL021331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167347472,"end":167348053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223635.1","gene_symbol":"AL121990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":229508501,"end":229514272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248774.1","gene_symbol":"AC097534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173322206,"end":173329694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109586.11","gene_symbol":"GALNT7","gene_name":"polypeptide N-acetylgalactosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4129]","synonyms":"GALNAC-T7","biotype":"protein_coding","ncbi_id":"51809","summary":"This gene encodes GalNAc transferase 7, a member of the GalNAc-transferase family. The enzyme encoded by this gene controls the initiation step of mucin-type O-linked protein glycosylation and transfer of N-acetylgalactosamine to serine and threonine amino acid residues. This enzyme is a type II transmembrane protein and shares common sequence motifs with other family members. Unlike other family members, this enzyme shows exclusive specificity for partially GalNAc-glycosylated acceptor substrates and shows no activity with non-glycosylated peptides. This protein may function as a follow-up enzyme in the initiation step of O-glycosylation. [provided by RefSeq, Jul 2008]","start":173168753,"end":173323967,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4129]"}, {"versioned_ensembl_gene_id":"ENSG00000077150.18","gene_symbol":"NFKB2","gene_name":"nuclear factor kappa B subunit 2 [Source:HGNC Symbol;Acc:HGNC:7795]","synonyms":"p52,p49/p100,p105,NF-kB2,LYT-10","biotype":"protein_coding","ncbi_id":"4791","summary":"This gene encodes a subunit of the transcription factor complex nuclear factor-kappa-B (NFkB). The NFkB complex is expressed in numerous cell types and functions as a central activator of genes involved in inflammation and immune function. The protein encoded by this gene can function as both a transcriptional activator or repressor depending on its dimerization partner. The p100 full-length protein is co-translationally processed into a p52 active form. Chromosomal rearrangements and translocations of this locus have been observed in B cell lymphomas, some of which may result in the formation of fusion proteins. There is a pseudogene for this gene on chromosome 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":102394110,"end":102402529,"strand":1,"description":"nuclear factor kappa B subunit 2 [Source:HGNC Symbol;Acc:HGNC:7795]"}, {"versioned_ensembl_gene_id":"ENSG00000260161.1","gene_symbol":"MTCYBP28","gene_name":"mitochondrially encoded cytochrome b pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:51994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075134","summary":null,"start":82120638,"end":82121769,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:51994]"}, {"versioned_ensembl_gene_id":"ENSG00000261235.1","gene_symbol":"AC092142.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82044336,"end":82139631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146047.6","gene_symbol":"HIST1H2BA","gene_name":"histone cluster 1 H2B family member a [Source:HGNC Symbol;Acc:HGNC:18730]","synonyms":"TSH2B,STBP,H2BFU,bA317E16.3","biotype":"protein_coding","ncbi_id":"255626","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a testis/sperm-specific member of the histone H2B family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":25726777,"end":25727292,"strand":1,"description":"histone cluster 1 H2B family member a [Source:HGNC Symbol;Acc:HGNC:18730]"}, {"versioned_ensembl_gene_id":"ENSG00000269038.1","gene_symbol":"AP001462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64778954,"end":64779405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169230.9","gene_symbol":"PRELID1","gene_name":"PRELI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30255]","synonyms":"PRELI,CGI-106,PX19","biotype":"protein_coding","ncbi_id":"27166","summary":"This gene encodes a member of the late embryogenesis abundant motif-containing protein family. The encoded protein is localized to mitochondria and may function as a cytoprotectant by regulating cell death and differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. Several related pseudogenes have been identified. [provided by RefSeq, Nov 2012]","start":177303774,"end":177306959,"strand":1,"description":"PRELI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30255]"}, {"versioned_ensembl_gene_id":"ENSG00000086696.10","gene_symbol":"HSD17B2","gene_name":"hydroxysteroid 17-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5211]","synonyms":"SDR9C2,HSD17","biotype":"protein_coding","ncbi_id":"3294","summary":null,"start":82035004,"end":82098534,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5211]"}, {"versioned_ensembl_gene_id":"ENSG00000170876.7","gene_symbol":"TMEM43","gene_name":"transmembrane protein 43 [Source:HGNC Symbol;Acc:HGNC:28472]","synonyms":"LUMA,DKFZp586G1919,ARVD5,MGC3222","biotype":"protein_coding","ncbi_id":"79188","summary":"This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC. [provided by RefSeq, Oct 2008]","start":14124940,"end":14143679,"strand":1,"description":"transmembrane protein 43 [Source:HGNC Symbol;Acc:HGNC:28472]"}, {"versioned_ensembl_gene_id":"ENSG00000143771.11","gene_symbol":"CNIH4","gene_name":"cornichon family AMPA receptor auxiliary protein 4 [Source:HGNC Symbol;Acc:HGNC:25013]","synonyms":"HSPC163","biotype":"protein_coding","ncbi_id":"29097","summary":null,"start":224356850,"end":224379459,"strand":1,"description":"cornichon family AMPA receptor auxiliary protein 4 [Source:HGNC Symbol;Acc:HGNC:25013]"}, {"versioned_ensembl_gene_id":"ENSG00000238148.2","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31242712,"end":31243133,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000048649.13","gene_symbol":"RSF1","gene_name":"remodeling and spacing factor 1 [Source:HGNC Symbol;Acc:HGNC:18118]","synonyms":"XAP8,RSF-1,p325,HBXAP","biotype":"protein_coding","ncbi_id":"51773","summary":"This gene encodes a nuclear protein that interacts with hepatitis B virus X protein (HBX) and facilitates transcription of hepatitis B virus genes by the HBX transcription activator, suggesting a role for this interaction in the virus life cycle. This protein also interacts with SNF2H protein to form the RSF chromatin-remodeling complex, where the SNF2H subunit functions as the nucleosome-dependent ATPase, and this protein as the histone chaperone. [provided by RefSeq, Sep 2011]","start":77659996,"end":77821017,"strand":-1,"description":"remodeling and spacing factor 1 [Source:HGNC Symbol;Acc:HGNC:18118]"}, {"versioned_ensembl_gene_id":"ENSG00000264189.1","gene_symbol":"AP005262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1927727,"end":1929094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264958.2","gene_symbol":"ALOX12P1","gene_name":"arachidonate 12-lipoxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:431]","synonyms":"ALOX12P","biotype":"unprocessed_pseudogene","ncbi_id":"243","summary":null,"start":30529688,"end":30542416,"strand":1,"description":"arachidonate 12-lipoxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:431]"}, {"versioned_ensembl_gene_id":"ENSG00000059378.12","gene_symbol":"PARP12","gene_name":"poly(ADP-ribose) polymerase family member 12 [Source:HGNC Symbol;Acc:HGNC:21919]","synonyms":"PARP-12,FLJ22693,ZC3HDC1,ZC3H1","biotype":"protein_coding","ncbi_id":"64761","summary":null,"start":140023744,"end":140063721,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 12 [Source:HGNC Symbol;Acc:HGNC:21919]"}, {"versioned_ensembl_gene_id":"ENSG00000228454.7","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"CO4,C4B3,CH,C4B1,CPAMD3,C4F","biotype":"protein_coding","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":32007416,"end":32028073,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000215601.3","gene_symbol":"TSPY24P","gene_name":"testis specific protein, Y-linked 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:38725]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874287","summary":null,"start":8280198,"end":8282209,"strand":1,"description":"testis specific protein, Y-linked 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:38725]"}, {"versioned_ensembl_gene_id":"ENSG00000267713.1","gene_symbol":"AC012433.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":50669510,"end":50670215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100146.16","gene_symbol":"SOX10","gene_name":"SRY-box 10 [Source:HGNC Symbol;Acc:HGNC:11190]","synonyms":"WS4,WS2E,DOM","biotype":"protein_coding","ncbi_id":"6663","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]","start":37970686,"end":37987422,"strand":-1,"description":"SRY-box 10 [Source:HGNC Symbol;Acc:HGNC:11190]"}, {"versioned_ensembl_gene_id":"ENSG00000151552.11","gene_symbol":"QDPR","gene_name":"quinoid dihydropteridine reductase [Source:HGNC Symbol;Acc:HGNC:9752]","synonyms":"PKU2,DHPR,SDR33C1","biotype":"protein_coding","ncbi_id":"5860","summary":"This gene encodes the enzyme dihydropteridine reductase, which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin. This enzyme is an essential component of the pterin-dependent aromatic amino acid hydroxylating systems. Mutations in this gene resulting in QDPR deficiency include aberrant splicing, amino acid substitutions, insertions, or premature terminations. Dihydropteridine reductase deficiency presents as atypical phenylketonuria due to insufficient production of biopterin, a cofactor for phenylalanine hydroxylase. [provided by RefSeq, Jul 2008]","start":17460261,"end":17512234,"strand":-1,"description":"quinoid dihydropteridine reductase [Source:HGNC Symbol;Acc:HGNC:9752]"}, {"versioned_ensembl_gene_id":"ENSG00000141639.11","gene_symbol":"MAPK4","gene_name":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]","synonyms":"Erk4,Erk3-related,PRKM4","biotype":"protein_coding","ncbi_id":"5596","summary":"Mitogen-activated protein kinase 4 is a member of the mitogen-activated protein kinase family. Tyrosine kinase growth factor receptors activate mitogen-activated protein kinases which then translocate into the nucleus and phosphorylate nuclear targets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":50560078,"end":50731824,"strand":1,"description":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]"}, {"versioned_ensembl_gene_id":"ENSG00000263674.1","gene_symbol":"AC026620.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32280387,"end":32280953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224634.1","gene_symbol":"ZNF736P6Y","gene_name":"zinc finger protein 736 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:38440]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419732","summary":null,"start":8350931,"end":8352143,"strand":1,"description":"zinc finger protein 736 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:38440]"}, {"versioned_ensembl_gene_id":"ENSG00000251162.1","gene_symbol":"AC074198.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164597719,"end":164597976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162769.12","gene_symbol":"FLVCR1","gene_name":"feline leukemia virus subgroup C cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:24682]","synonyms":"PCA,MFSD7B,FLVCR,AXPC1","biotype":"protein_coding","ncbi_id":"28982","summary":"This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein is a heme transporter that may play a critical role in erythropoiesis by protecting developing erythroid cells from heme toxicity. This gene may play a role in posterior column ataxia with retinitis pigmentosa and the hematological disorder Diamond-Blackfan syndrome. [provided by RefSeq, Jan 2011]","start":212858255,"end":212899363,"strand":1,"description":"feline leukemia virus subgroup C cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:24682]"}, {"versioned_ensembl_gene_id":"ENSG00000248766.2","gene_symbol":"AC093303.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20158662,"end":20158956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141314.12","gene_symbol":"RHBDL3","gene_name":"rhomboid like 3 [Source:HGNC Symbol;Acc:HGNC:16502]","synonyms":"VRHO,RHBDL4","biotype":"protein_coding","ncbi_id":"162494","summary":null,"start":32266176,"end":32324661,"strand":1,"description":"rhomboid like 3 [Source:HGNC Symbol;Acc:HGNC:16502]"}, {"versioned_ensembl_gene_id":"ENSG00000261668.1","gene_symbol":"AC093591.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127840198,"end":127844040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214132.4","gene_symbol":"AC094103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20304045,"end":20305448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137094.14","gene_symbol":"DNAJB5","gene_name":"DnaJ heat shock protein family (Hsp40) member B5 [Source:HGNC Symbol;Acc:HGNC:14887]","synonyms":"Hsc40","biotype":"protein_coding","ncbi_id":"25822","summary":"This gene encodes a member of the DNAJ heat shock protein 40 family of co-chaperone proteins. The encoded protein contains an N-terminal DNAJ domain and a C-terminal substrate binding domain but lacks the cysteine-rich domain found in other DNAJ family members. In mice, a multi-protein complex containing this protein, thioredoxin 1, and histone deacetylase 4, serves as a master negative regulator of cardiac hypertrophy. [provided by RefSeq, Mar 2017]","start":34989641,"end":34998900,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B5 [Source:HGNC Symbol;Acc:HGNC:14887]"}, {"versioned_ensembl_gene_id":"ENSG00000244021.4","gene_symbol":"AC093591.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127812720,"end":127813200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124570.17","gene_symbol":"SERPINB6","gene_name":"serpin family B member 6 [Source:HGNC Symbol;Acc:HGNC:8950]","synonyms":"PTI,PI6,DFNB91,CAP","biotype":"protein_coding","ncbi_id":"5269","summary":"The protein encoded by this gene is a member of the serpin (serine proteinase inhibitor) superfamily, and ovalbumin(ov)-serpin subfamily. It was originally discovered as a placental thrombin inhibitor. The mouse homolog was found to be expressed in the hair cells of the inner ear. Mutations in this gene are associated with nonsyndromic progressive hearing loss, suggesting that this serpin plays an important role in the inner ear in the protection against leakage of lysosomal content during stress, and that loss of this protection results in cell death and sensorineural hearing loss. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]","start":2948159,"end":2972165,"strand":-1,"description":"serpin family B member 6 [Source:HGNC Symbol;Acc:HGNC:8950]"}, {"versioned_ensembl_gene_id":"ENSG00000249854.1","gene_symbol":"CDH18-AS1","gene_name":"CDH18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53088]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102725105","summary":null,"start":20305565,"end":20331456,"strand":1,"description":"CDH18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53088]"}, {"versioned_ensembl_gene_id":"ENSG00000282855.1","gene_symbol":"AC093591.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127809170,"end":127809477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145526.11","gene_symbol":"CDH18","gene_name":"cadherin 18 [Source:HGNC Symbol;Acc:HGNC:1757]","synonyms":"EY-CADHERIN,CDH14","biotype":"protein_coding","ncbi_id":"1016","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily of integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. This particular cadherin is expressed specifically in the central nervous system and is putatively involved in synaptic adhesion, axon outgrowth and guidance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":19472951,"end":20575873,"strand":-1,"description":"cadherin 18 [Source:HGNC Symbol;Acc:HGNC:1757]"}, {"versioned_ensembl_gene_id":"ENSG00000164070.11","gene_symbol":"HSPA4L","gene_name":"heat shock protein family A (Hsp70) member 4 like [Source:HGNC Symbol;Acc:HGNC:17041]","synonyms":"Osp94,HSPH3,APG-1","biotype":"protein_coding","ncbi_id":"22824","summary":"The protein encoded by this gene is heat shock inducible and may act as a chaperone. The encoded protein can protect the heat-shocked cell against the harmful effects of aggregated proteins. This gene is highly expressed in leukemia cells and may be a good target for therapeutic intervention. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":127781821,"end":127840733,"strand":1,"description":"heat shock protein family A (Hsp70) member 4 like [Source:HGNC Symbol;Acc:HGNC:17041]"}, {"versioned_ensembl_gene_id":"ENSG00000245213.6","gene_symbol":"AC105285.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173131928,"end":173169652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260022.1","gene_symbol":"AL031716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":883780,"end":885090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276931.1","gene_symbol":"AC009041.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":968375,"end":969012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230051.1","gene_symbol":"AL020994.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27331787,"end":27379265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103227.18","gene_symbol":"LMF1","gene_name":"lipase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:14154]","synonyms":"TMEM112A,TMEM112,JFP11,FLJ22302,FLJ12681,C16orf26","biotype":"protein_coding","ncbi_id":"64788","summary":null,"start":853634,"end":981318,"strand":-1,"description":"lipase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:14154]"}, {"versioned_ensembl_gene_id":"ENSG00000233597.3","gene_symbol":"AC133435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142043623,"end":142044198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280445.1","gene_symbol":"AL049536.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27414462,"end":27419713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167105.7","gene_symbol":"TMEM92","gene_name":"transmembrane protein 92 [Source:HGNC Symbol;Acc:HGNC:26579]","synonyms":"FLJ33318","biotype":"protein_coding","ncbi_id":"162461","summary":null,"start":50271406,"end":50281485,"strand":1,"description":"transmembrane protein 92 [Source:HGNC Symbol;Acc:HGNC:26579]"}, {"versioned_ensembl_gene_id":"ENSG00000227880.1","gene_symbol":"AL050402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27457247,"end":27460060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114126.17","gene_symbol":"TFDP2","gene_name":"transcription factor Dp-2 [Source:HGNC Symbol;Acc:HGNC:11751]","synonyms":"Dp-2","biotype":"protein_coding","ncbi_id":"7029","summary":"The gene is a member of the transcription factor DP family. The encoded protein forms heterodimers with the E2F transcription factors resulting in transcriptional activation of cell cycle regulated genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":141944428,"end":142149544,"strand":-1,"description":"transcription factor Dp-2 [Source:HGNC Symbol;Acc:HGNC:11751]"}, {"versioned_ensembl_gene_id":"ENSG00000231788.4","gene_symbol":"RPL31P50","gene_name":"ribosomal protein L31 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341356","summary":null,"start":31597114,"end":31597409,"strand":-1,"description":"ribosomal protein L31 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36799]"}, {"versioned_ensembl_gene_id":"ENSG00000203437.3","gene_symbol":"AC022080.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31465062,"end":31465842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256159.1","gene_symbol":"AC022080.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31477506,"end":31477987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226250.1","gene_symbol":"LINC00408","gene_name":"long intergenic non-protein coding RNA 408 [Source:HGNC Symbol;Acc:HGNC:42740]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652856","summary":null,"start":18905439,"end":18907810,"strand":1,"description":"long intergenic non-protein coding RNA 408 [Source:HGNC Symbol;Acc:HGNC:42740]"}, {"versioned_ensembl_gene_id":"ENSG00000279010.3","gene_symbol":"AL031587.6","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":37948352,"end":38002889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231358.2","gene_symbol":"AL355516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18921889,"end":18923765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272582.1","gene_symbol":"AL031587.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37950965,"end":37951778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270975.1","gene_symbol":"MAGOH3P","gene_name":"mago homolog 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:20020]","synonyms":"MAGOHP1,MAGOHP","biotype":"unprocessed_pseudogene","ncbi_id":"90352","summary":null,"start":68861762,"end":68862525,"strand":1,"description":"mago homolog 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:20020]"}, {"versioned_ensembl_gene_id":"ENSG00000226599.1","gene_symbol":"AL450344.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150650772,"end":150652025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227139.1","gene_symbol":"AC241644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147697794,"end":147699335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069424.14","gene_symbol":"KCNAB2","gene_name":"potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6229]","synonyms":"KCNA2B,HKvbeta2.2,HKvbeta2.1,AKR6A5","biotype":"protein_coding","ncbi_id":"8514","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member is one of the beta subunits, which are auxiliary proteins associating with functional Kv-alpha subunits. This member alters functional properties of the KCNA4 gene product. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2010]","start":5991466,"end":6101193,"strand":1,"description":"potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6229]"}, {"versioned_ensembl_gene_id":"ENSG00000278948.1","gene_symbol":"AL031587.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37943050,"end":37944898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169228.13","gene_symbol":"RAB24","gene_name":"RAB24, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53917","summary":"RAB24 is a small GTPase of the Rab subfamily of Ras-related proteins that regulate intracellular protein trafficking (Olkkonen et al., 1993 [PubMed 8126105]).[supplied by OMIM, Aug 2009]","start":177301198,"end":177303744,"strand":-1,"description":"RAB24, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9765]"}, {"versioned_ensembl_gene_id":"ENSG00000128346.10","gene_symbol":"C22orf23","gene_name":"chromosome 22 open reading frame 23 [Source:HGNC Symbol;Acc:HGNC:18589]","synonyms":"FLJ32787,EVG1,LOC84645","biotype":"protein_coding","ncbi_id":"84645","summary":null,"start":37943050,"end":37953669,"strand":-1,"description":"chromosome 22 open reading frame 23 [Source:HGNC Symbol;Acc:HGNC:18589]"}, {"versioned_ensembl_gene_id":"ENSG00000230918.1","gene_symbol":"AC008063.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162073256,"end":162075169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268649.5","gene_symbol":"AL132655.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58817132,"end":58817725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263201.1","gene_symbol":"AC040162.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":68013436,"end":68015911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270872.2","gene_symbol":"SRGAP2D","gene_name":"SLIT-ROBO Rho GTPase activating protein 2D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43932]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996712","summary":"This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. This human-specific locus resulted from segmental duplication of the SLIT-ROBO Rho GTPase activating protein 2B locus. This duplicated locus lacks an internal exon, and thus this gene copy may not be functional. Expression of this locus appears to be much lower than the similar SLIT-ROBO Rho GTPase activating protein 2C (SRGAP2C) locus. The SRGAP2C locus has been shown to encode a protein that functions antagonistically to SLIT-ROBO Rho GTPase activating protein 2 in cortical neuron development. [provided by RefSeq, May 2014]","start":143975087,"end":144068350,"strand":1,"description":"SLIT-ROBO Rho GTPase activating protein 2D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43932]"}, {"versioned_ensembl_gene_id":"ENSG00000257043.1","gene_symbol":"AP006296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18665050,"end":18665548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262514.1","gene_symbol":"AC020978.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68199795,"end":68200981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128944.13","gene_symbol":"KNSTRN","gene_name":"kinetochore localized astrin/SPAG5 binding protein [Source:HGNC Symbol;Acc:HGNC:30767]","synonyms":"TRAF4AF1,SKAP,kinastrin,FLJ14502,C15orf23","biotype":"protein_coding","ncbi_id":"90417","summary":null,"start":40382721,"end":40394246,"strand":1,"description":"kinetochore localized astrin/SPAG5 binding protein [Source:HGNC Symbol;Acc:HGNC:30767]"}, {"versioned_ensembl_gene_id":"ENSG00000262160.1","gene_symbol":"AC020978.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68225969,"end":68229145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110436.11","gene_symbol":"SLC1A2","gene_name":"solute carrier family 1 member 2 [Source:HGNC Symbol;Acc:HGNC:10940]","synonyms":"EAAT2,GLT-1","biotype":"protein_coding","ncbi_id":"6506","summary":"This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Improper regulation of this gene is thought to be associated with several neurological disorders. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2017]","start":35251206,"end":35420063,"strand":-1,"description":"solute carrier family 1 member 2 [Source:HGNC Symbol;Acc:HGNC:10940]"}, {"versioned_ensembl_gene_id":"ENSG00000103067.13","gene_symbol":"ESRP2","gene_name":"epithelial splicing regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:26152]","synonyms":"RBM35B,FLJ21918","biotype":"protein_coding","ncbi_id":"80004","summary":"ESPR2 is an epithelial cell-type-specific splicing regulator (Warzecha et al., 2009 [PubMed 19285943]).[supplied by OMIM, Aug 2009]","start":68229111,"end":68238102,"strand":-1,"description":"epithelial splicing regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:26152]"}, {"versioned_ensembl_gene_id":"ENSG00000214417.4","gene_symbol":"KRT18P13","gene_name":"keratin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6432]","synonyms":"KRT18L3","biotype":"processed_pseudogene","ncbi_id":"392371","summary":null,"start":97698922,"end":97700734,"strand":1,"description":"keratin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6432]"}, {"versioned_ensembl_gene_id":"ENSG00000260677.1","gene_symbol":"AL445531.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97743208,"end":97744935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236130.1","gene_symbol":"PTCSC2","gene_name":"papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44086]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928337","summary":null,"start":97805935,"end":97810008,"strand":-1,"description":"papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44086]"}, {"versioned_ensembl_gene_id":"ENSG00000165030.3","gene_symbol":"NFIL3","gene_name":"nuclear factor, interleukin 3 regulated [Source:HGNC Symbol;Acc:HGNC:7787]","synonyms":"NFIL3A,NF-IL3A,IL3BP1,E4BP4","biotype":"protein_coding","ncbi_id":"4783","summary":"The protein encoded by this gene is a transcriptional regulator that binds as a homodimer to activating transcription factor (ATF) sites in many cellular and viral promoters. The encoded protein represses PER1 and PER2 expression and therefore plays a role in the regulation of circadian rhythm. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2014]","start":91409045,"end":91423862,"strand":-1,"description":"nuclear factor, interleukin 3 regulated [Source:HGNC Symbol;Acc:HGNC:7787]"}, {"versioned_ensembl_gene_id":"ENSG00000082515.17","gene_symbol":"MRPL22","gene_name":"mitochondrial ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:14480]","synonyms":"RPML25,MRP-L25,HSPC158","biotype":"protein_coding","ncbi_id":"29093","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L22 ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 4q. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":154941070,"end":154969411,"strand":1,"description":"mitochondrial ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:14480]"}, {"versioned_ensembl_gene_id":"ENSG00000232685.4","gene_symbol":"LINC00442","gene_name":"long intergenic non-protein coding RNA 442 [Source:HGNC Symbol;Acc:HGNC:42779]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"348021","summary":null,"start":19008259,"end":19012559,"strand":1,"description":"long intergenic non-protein coding RNA 442 [Source:HGNC Symbol;Acc:HGNC:42779]"}, {"versioned_ensembl_gene_id":"ENSG00000120645.11","gene_symbol":"IQSEC3","gene_name":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]","synonyms":"KIAA1110,MGC30156","biotype":"protein_coding","ncbi_id":"440073","summary":null,"start":66765,"end":178460,"strand":1,"description":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]"}, {"versioned_ensembl_gene_id":"ENSG00000178919.8","gene_symbol":"FOXE1","gene_name":"forkhead box E1 [Source:HGNC Symbol;Acc:HGNC:3806]","synonyms":"FOXE2,FKHL15,TTF-2,TITF2,HFKH4","biotype":"protein_coding","ncbi_id":"2304","summary":"This intronless gene encodes a protein that belongs to the forkhead family of transcription factors. Members of this family contain a conserved 100-amino acid DNA-binding 'forkhead' domain. The encoded protein functions as a thyroid transcription factor that plays a role in thyroid morphogenesis. Mutations in this gene are associated with the Bamforth-Lazarus syndrome, and with susceptibility to nonmedullary thyroid cancer-4. [provided by RefSeq, Nov 2016]","start":97853254,"end":97856715,"strand":1,"description":"forkhead box E1 [Source:HGNC Symbol;Acc:HGNC:3806]"}, {"versioned_ensembl_gene_id":"ENSG00000188917.14","gene_symbol":"TRMT2B","gene_name":"tRNA methyltransferase 2 homolog B [Source:HGNC Symbol;Acc:HGNC:25748]","synonyms":"FLJ12687,CXorf34","biotype":"protein_coding","ncbi_id":"79979","summary":"This gene encodes a homolog of the TRM2 gene in S. cerevisiae. The yeast gene encodes a tRNA methyltransferase that plays a role in tRNA maturation. The yeast protein also has endo-exonuclease activity and may be involved in DNA double strand break repair. Alternative splicing results in multiple transcripts encoding different isoforms. [provided by RefSeq, Nov 2009]","start":101009346,"end":101052116,"strand":-1,"description":"tRNA methyltransferase 2 homolog B [Source:HGNC Symbol;Acc:HGNC:25748]"}, {"versioned_ensembl_gene_id":"ENSG00000179088.14","gene_symbol":"C12orf42","gene_name":"chromosome 12 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:24729]","synonyms":"FLJ25323","biotype":"protein_coding","ncbi_id":"374470","summary":null,"start":103237591,"end":103496010,"strand":-1,"description":"chromosome 12 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:24729]"}, {"versioned_ensembl_gene_id":"ENSG00000227376.1","gene_symbol":"FTH1P16","gene_name":"ferritin heavy chain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:3986]","synonyms":"FTHL16,FTH2","biotype":"processed_pseudogene","ncbi_id":"2508","summary":null,"start":77734475,"end":77735026,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:3986]"}, {"versioned_ensembl_gene_id":"ENSG00000263860.1","gene_symbol":"AC011840.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30550493,"end":30551189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255409.1","gene_symbol":"RSF1-IT1","gene_name":"RSF1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41439]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874308","summary":null,"start":77738680,"end":77739568,"strand":-1,"description":"RSF1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41439]"}, {"versioned_ensembl_gene_id":"ENSG00000219622.1","gene_symbol":"AL451061.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150504811,"end":150510300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219529.2","gene_symbol":"AP000580.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77813319,"end":77813676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254985.1","gene_symbol":"RSF1-IT2","gene_name":"RSF1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41438]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874307","summary":null,"start":77717712,"end":77718411,"strand":-1,"description":"RSF1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41438]"}, {"versioned_ensembl_gene_id":"ENSG00000170860.3","gene_symbol":"LSM3","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17874]","synonyms":"YLR438C,USS2,SMX4","biotype":"protein_coding","ncbi_id":"27258","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]","start":14178358,"end":14201119,"strand":1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17874]"}, {"versioned_ensembl_gene_id":"ENSG00000136932.13","gene_symbol":"TRMO","gene_name":"tRNA methyltransferase O [Source:HGNC Symbol;Acc:HGNC:30967]","synonyms":"HSPC219,C9orf156","biotype":"protein_coding","ncbi_id":"51531","summary":null,"start":97904489,"end":97922570,"strand":-1,"description":"tRNA methyltransferase O [Source:HGNC Symbol;Acc:HGNC:30967]"}, {"versioned_ensembl_gene_id":"ENSG00000279431.1","gene_symbol":"AC011840.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30551193,"end":30551802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164880.15","gene_symbol":"INTS1","gene_name":"integrator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24555]","synonyms":"NET28,KIAA1440,INT1,DKFZp586J0619","biotype":"protein_coding","ncbi_id":"26173","summary":"INTS1 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":1470277,"end":1504367,"strand":-1,"description":"integrator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24555]"}, {"versioned_ensembl_gene_id":"ENSG00000233081.1","gene_symbol":"AL353764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91426238,"end":91427144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086504.15","gene_symbol":"MRPL28","gene_name":"mitochondrial ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:14484]","synonyms":"p15,MAAT1","biotype":"protein_coding","ncbi_id":"10573","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein, a part of which was originally isolated by its ability to recognize tyrosinase in an HLA-A24-restricted fashion. [provided by RefSeq, Jul 2008]","start":367384,"end":370527,"strand":-1,"description":"mitochondrial ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:14484]"}, {"versioned_ensembl_gene_id":"ENSG00000108666.9","gene_symbol":"C17orf75","gene_name":"chromosome 17 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:30173]","synonyms":"SRI2,NJMU-R1","biotype":"protein_coding","ncbi_id":"64149","summary":null,"start":32324565,"end":32350023,"strand":-1,"description":"chromosome 17 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:30173]"}, {"versioned_ensembl_gene_id":"ENSG00000266733.5","gene_symbol":"TBC1D29","gene_name":"TBC1 domain family member 29 [Source:HGNC Symbol;Acc:HGNC:24509]","synonyms":"DKFZP434O047","biotype":"protein_coding","ncbi_id":"26083","summary":null,"start":30557112,"end":30563493,"strand":1,"description":"TBC1 domain family member 29 [Source:HGNC Symbol;Acc:HGNC:24509]"}, {"versioned_ensembl_gene_id":"ENSG00000222044.1","gene_symbol":"AL031587.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38032165,"end":38034228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135776.4","gene_symbol":"ABCB10","gene_name":"ATP binding cassette subfamily B member 10 [Source:HGNC Symbol;Acc:HGNC:41]","synonyms":"MTABC2,M-ABC2,EST20237","biotype":"protein_coding","ncbi_id":"23456","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The function of this mitochondrial protein is unknown. [provided by RefSeq, Jul 2008]","start":229516582,"end":229558695,"strand":-1,"description":"ATP binding cassette subfamily B member 10 [Source:HGNC Symbol;Acc:HGNC:41]"}, {"versioned_ensembl_gene_id":"ENSG00000264765.1","gene_symbol":"AC098850.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16653904,"end":16654787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264359.1","gene_symbol":"NEK4P2","gene_name":"NIMA-related kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39650]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421734","summary":null,"start":16666107,"end":16667118,"strand":-1,"description":"NIMA-related kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39650]"}, {"versioned_ensembl_gene_id":"ENSG00000260569.2","gene_symbol":"AC090398.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74211391,"end":74240555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231458.2","gene_symbol":"AC098850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16683438,"end":16684227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178762.4","gene_symbol":"HIST1H2BPS1","gene_name":"histone cluster 1 H2B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18719]","synonyms":"H2BFVP,bA317E16.4","biotype":"unprocessed_pseudogene","ncbi_id":"100288742","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 6. [provided by RefSeq, Oct 2015]","start":25731782,"end":25732091,"strand":-1,"description":"histone cluster 1 H2B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18719]"}, {"versioned_ensembl_gene_id":"ENSG00000075624.13","gene_symbol":"ACTB","gene_name":"actin beta [Source:HGNC Symbol;Acc:HGNC:132]","synonyms":null,"biotype":"protein_coding","ncbi_id":"60","summary":"This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome. [provided by RefSeq, Aug 2017]","start":5527151,"end":5563784,"strand":-1,"description":"actin beta [Source:HGNC Symbol;Acc:HGNC:132]"}, {"versioned_ensembl_gene_id":"ENSG00000216436.2","gene_symbol":"AL512384.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25732497,"end":25732827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185339.8","gene_symbol":"TCN2","gene_name":"transcobalamin 2 [Source:HGNC Symbol;Acc:HGNC:11653]","synonyms":"TC2,D22S750,D22S676","biotype":"protein_coding","ncbi_id":"6948","summary":"This gene encodes a member of the vitamin B12-binding protein family. This family of proteins, alternatively referred to as R binders, is expressed in various tissues and secretions. This plasma protein binds cobalamin and mediates the transport of cobalamin into cells. This protein and other mammalian cobalamin-binding proteins, such as transcobalamin I and gastric intrisic factor, may have evolved by duplication of a common ancestral gene. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":30606838,"end":30627278,"strand":1,"description":"transcobalamin 2 [Source:HGNC Symbol;Acc:HGNC:11653]"}, {"versioned_ensembl_gene_id":"ENSG00000223767.5","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"G16,RING5,RMA1,NG2","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32245363,"end":32247802,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000118432.12","gene_symbol":"CNR1","gene_name":"cannabinoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:2159]","synonyms":"CNR,CB1K5,CB1A,CB1,CB-R,CANN6","biotype":"protein_coding","ncbi_id":"1268","summary":"This gene encodes one of two cannabinoid receptors. The cannabinoids, principally delta-9-tetrahydrocannabinol and synthetic analogs, are psychoactive ingredients of marijuana. The cannabinoid receptors are members of the guanine-nucleotide-binding protein (G-protein) coupled receptor family, which inhibit adenylate cyclase activity in a dose-dependent, stereoselective and pertussis toxin-sensitive manner. The two receptors have been found to be involved in the cannabinoid-induced CNS effects (including alterations in mood and cognition) experienced by users of marijuana. Multiple transcript variants encoding two different protein isoforms have been described for this gene. [provided by RefSeq, May 2009]","start":88139864,"end":88166359,"strand":-1,"description":"cannabinoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:2159]"}, {"versioned_ensembl_gene_id":"ENSG00000154767.14","gene_symbol":"XPC","gene_name":"XPC complex subunit, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12816]","synonyms":"XPCC,RAD4","biotype":"protein_coding","ncbi_id":"7508","summary":"The protein encoded by this gene is a key component of the XPC complex, which plays an important role in the early steps of global genome nucleotide excision repair (NER). The encoded protein is important for damage sensing and DNA binding, and shows a preference for single-stranded DNA. Mutations in this gene or some other NER components can result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]","start":14145147,"end":14178783,"strand":-1,"description":"XPC complex subunit, DNA damage recognition and repair factor [Source:HGNC Symbol;Acc:HGNC:12816]"}, {"versioned_ensembl_gene_id":"ENSG00000185650.9","gene_symbol":"ZFP36L1","gene_name":"ZFP36 ring finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:1107]","synonyms":"TIS11B,RNF162B,ERF1,cMG1,BRF1,Berg36","biotype":"protein_coding","ncbi_id":"677","summary":"This gene is a member of the TIS11 family of early response genes, which are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. This gene is well conserved across species and has a promoter that contains motifs seen in other early-response genes. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":68787660,"end":68796253,"strand":-1,"description":"ZFP36 ring finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:1107]"}, {"versioned_ensembl_gene_id":"ENSG00000089123.15","gene_symbol":"TASP1","gene_name":"taspase 1 [Source:HGNC Symbol;Acc:HGNC:15859]","synonyms":"dJ585I14.2,C20orf13,FLJ20212","biotype":"protein_coding","ncbi_id":"55617","summary":"This gene encodes an endopeptidase that cleaves specific substrates following aspartate residues. The encoded protein undergoes posttranslational autoproteolytic processing to generate alpha and beta subunits, which reassemble into the active alpha2-beta2 heterotetramer. It is required to cleave MLL, a protein required for the maintenance of HOX gene expression, and TFIIA, a basal transcription factor. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":13389392,"end":13638940,"strand":-1,"description":"taspase 1 [Source:HGNC Symbol;Acc:HGNC:15859]"}, {"versioned_ensembl_gene_id":"ENSG00000266775.1","gene_symbol":"AC011840.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30557732,"end":30558502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264242.2","gene_symbol":"AC011840.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30553697,"end":30558962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280010.1","gene_symbol":"AP001350.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58627435,"end":58628528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242686.4","gene_symbol":"AC107464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":652850,"end":656213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251012.1","gene_symbol":"AC083800.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":119147375,"end":119187807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254588.1","gene_symbol":"AP003397.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128526142,"end":128530389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163424.8","gene_symbol":"C3orf30","gene_name":"chromosome 3 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:26553]","synonyms":"TSCPA,FLJ32859","biotype":"protein_coding","ncbi_id":"152405","summary":null,"start":119146150,"end":119160042,"strand":1,"description":"chromosome 3 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:26553]"}, {"versioned_ensembl_gene_id":"ENSG00000134954.14","gene_symbol":"ETS1","gene_name":"ETS proto-oncogene 1, transcription factor [Source:HGNC Symbol;Acc:HGNC:3488]","synonyms":"FLJ10768,EWSR2,ETS-1","biotype":"protein_coding","ncbi_id":"2113","summary":"This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":128458761,"end":128587558,"strand":-1,"description":"ETS proto-oncogene 1, transcription factor [Source:HGNC Symbol;Acc:HGNC:3488]"}, {"versioned_ensembl_gene_id":"ENSG00000100395.14","gene_symbol":"L3MBTL2","gene_name":"L3MBTL2, polycomb repressive complex 1 subunit [Source:HGNC Symbol;Acc:HGNC:18594]","synonyms":"dJ756G23.3,H-l(3)mbt-l,DKFZP761I141","biotype":"protein_coding","ncbi_id":"83746","summary":null,"start":41205205,"end":41231271,"strand":1,"description":"L3MBTL2, polycomb repressive complex 1 subunit [Source:HGNC Symbol;Acc:HGNC:18594]"}, {"versioned_ensembl_gene_id":"ENSG00000227784.1","gene_symbol":"ZNF965P","gene_name":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132598","summary":null,"start":18734080,"end":18734896,"strand":1,"description":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]"}, {"versioned_ensembl_gene_id":"ENSG00000279445.2","gene_symbol":"AC135068.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21683038,"end":21683962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249084.1","gene_symbol":"AC027627.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177343004,"end":177357032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176435.6","gene_symbol":"CLEC14A","gene_name":"C-type lectin domain containing 14A [Source:HGNC Symbol;Acc:HGNC:19832]","synonyms":"C14orf27","biotype":"protein_coding","ncbi_id":"161198","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This family member plays a role in cell-cell adhesion and angiogenesis. It functions in filopodia formation, cell migration and tube formation. Due to its presence at higher levels in tumor endothelium than in normal tissue endothelium, it is considered to be a candidate for tumor vascular targeting. [provided by RefSeq, Jan 2012]","start":38254103,"end":38256369,"strand":-1,"description":"C-type lectin domain containing 14A [Source:HGNC Symbol;Acc:HGNC:19832]"}, {"versioned_ensembl_gene_id":"ENSG00000120278.15","gene_symbol":"PLEKHG1","gene_name":"pleckstrin homology and RhoGEF domain containing G1 [Source:HGNC Symbol;Acc:HGNC:20884]","synonyms":"KIAA1209,ARHGEF41","biotype":"protein_coding","ncbi_id":"57480","summary":null,"start":150599883,"end":150843665,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G1 [Source:HGNC Symbol;Acc:HGNC:20884]"}, {"versioned_ensembl_gene_id":"ENSG00000259072.1","gene_symbol":"AL161751.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38290953,"end":38311930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174225.14","gene_symbol":"ARL13A","gene_name":"ADP ribosylation factor like GTPase 13A [Source:HGNC Symbol;Acc:HGNC:31709]","synonyms":"ARL13","biotype":"protein_coding","ncbi_id":"392509","summary":null,"start":100969708,"end":100990829,"strand":1,"description":"ADP ribosylation factor like GTPase 13A [Source:HGNC Symbol;Acc:HGNC:31709]"}, {"versioned_ensembl_gene_id":"ENSG00000271468.1","gene_symbol":"AL357094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38605255,"end":38606098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240435.2","gene_symbol":"AC020978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68209442,"end":68209778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273664.1","gene_symbol":"AC010776.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59700523,"end":59700946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224161.3","gene_symbol":"AC098847.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59761558,"end":59761905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274583.1","gene_symbol":"FAM74A4","gene_name":"family with sequence similarity 74 member A4 [Source:HGNC Symbol;Acc:HGNC:32032]","synonyms":"FLJ45202,FAM74A2","biotype":"transcribed_processed_pseudogene","ncbi_id":"401508","summary":null,"start":61205258,"end":61212373,"strand":1,"description":"family with sequence similarity 74 member A4 [Source:HGNC Symbol;Acc:HGNC:32032]"}, {"versioned_ensembl_gene_id":"ENSG00000279368.1","gene_symbol":"AL031123.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6685148,"end":6686984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114638.7","gene_symbol":"UPK1B","gene_name":"uroplakin 1B [Source:HGNC Symbol;Acc:HGNC:12578]","synonyms":"UPK1,TSPAN20","biotype":"protein_coding","ncbi_id":"7348","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is found in the asymmetrical unit membrane (AUM) where it can form a complex with other transmembrane 4 superfamily proteins. It may play a role in normal bladder epithelial physiology, possibly in regulating membrane permeability of superficial umbrella cells or in stabilizing the apical membrane through AUM/cytoskeletal interactions. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":119173517,"end":119205153,"strand":1,"description":"uroplakin 1B [Source:HGNC Symbol;Acc:HGNC:12578]"}, {"versioned_ensembl_gene_id":"ENSG00000255327.1","gene_symbol":"AP003062.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134950708,"end":134951568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249791.1","gene_symbol":"AC008494.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115188563,"end":115188932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267486.1","gene_symbol":"GLUD1P4","gene_name":"glutamate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4339]","synonyms":"GLUDP4","biotype":"processed_pseudogene","ncbi_id":"2750","summary":null,"start":59778572,"end":59778989,"strand":1,"description":"glutamate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4339]"}, {"versioned_ensembl_gene_id":"ENSG00000167264.17","gene_symbol":"DUS2","gene_name":"dihydrouridine synthase 2 [Source:HGNC Symbol;Acc:HGNC:26014]","synonyms":"FLJ20399,DUS2L,SMM1","biotype":"protein_coding","ncbi_id":"54920","summary":"This gene encodes a cytoplasmic protein that catalyzes the conversion of uridine residues to dihydrouridine in the D-loop of tRNA. The resulting modified bases confer enhanced regional flexibility to tRNA. The encoded protein may increase the rate of translation by inhibiting an interferon-induced protein kinase. This gene has been implicated in pulmonary carcinogenesis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":67987746,"end":68079320,"strand":1,"description":"dihydrouridine synthase 2 [Source:HGNC Symbol;Acc:HGNC:26014]"}, {"versioned_ensembl_gene_id":"ENSG00000279046.1","gene_symbol":"AP003062.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134985683,"end":134986799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258948.2","gene_symbol":"KRT8P1","gene_name":"keratin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20281]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338017","summary":null,"start":38727275,"end":38728481,"strand":1,"description":"keratin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20281]"}, {"versioned_ensembl_gene_id":"ENSG00000255512.1","gene_symbol":"AP005135.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135061781,"end":135075899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271581.1","gene_symbol":"AL671883.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31356647,"end":31357637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251179.1","gene_symbol":"TMEM92-AS1","gene_name":"TMEM92 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50442]","synonyms":"TCONS_00025237,RP11-893F2.9,lncRNA-508851","biotype":"antisense_RNA","ncbi_id":"103752589","summary":null,"start":50281577,"end":50287855,"strand":-1,"description":"TMEM92 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50442]"}, {"versioned_ensembl_gene_id":"ENSG00000226281.2","gene_symbol":"AL031123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6692744,"end":6711002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227939.1","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31280317,"end":31281519,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000275676.1","gene_symbol":"BX005040.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61229913,"end":61231863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233644.1","gene_symbol":"ARHGEF7-IT1","gene_name":"ARHGEF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41408]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874371","summary":null,"start":111122652,"end":111144264,"strand":1,"description":"ARHGEF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41408]"}, {"versioned_ensembl_gene_id":"ENSG00000204525.16","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31268749,"end":31272130,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000176160.10","gene_symbol":"HSF5","gene_name":"heat shock transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:26862]","synonyms":"FLJ40311","biotype":"protein_coding","ncbi_id":"124535","summary":null,"start":58420167,"end":58488384,"strand":-1,"description":"heat shock transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:26862]"}, {"versioned_ensembl_gene_id":"ENSG00000282156.1","gene_symbol":"AL512324.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45187292,"end":45198323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206299.8","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"ABCB3,PSF2,D6S217E,RING11","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32750528,"end":32767476,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000283378.1","gene_symbol":"BX088645.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61330717,"end":61453030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260439.1","gene_symbol":"LMF1-AS1","gene_name":"LMF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50469]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929387","summary":null,"start":921033,"end":934495,"strand":1,"description":"LMF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50469]"}, {"versioned_ensembl_gene_id":"ENSG00000276674.1","gene_symbol":"IGKV1OR1-1","gene_name":"immunoglobulin kappa variable 1/OR1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5764]","synonyms":"IGKVP1,IGKV1/OR1-1","biotype":"IG_V_pseudogene","ncbi_id":"3525","summary":null,"start":144085628,"end":144086098,"strand":1,"description":"immunoglobulin kappa variable 1/OR1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5764]"}, {"versioned_ensembl_gene_id":"ENSG00000224029.1","gene_symbol":"AL450344.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":150624677,"end":150626086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227352.1","gene_symbol":"ARHGEF7-AS1","gene_name":"ARHGEF7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39816]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874226","summary":null,"start":111144305,"end":111144733,"strand":-1,"description":"ARHGEF7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39816]"}, {"versioned_ensembl_gene_id":"ENSG00000224532.2","gene_symbol":"AL136361.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6758276,"end":6759291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126950.7","gene_symbol":"TMEM35A","gene_name":"transmembrane protein 35A [Source:HGNC Symbol;Acc:HGNC:25864]","synonyms":"TMEM35,FLJ14084","biotype":"protein_coding","ncbi_id":"59353","summary":null,"start":101078720,"end":101096364,"strand":1,"description":"transmembrane protein 35A [Source:HGNC Symbol;Acc:HGNC:25864]"}, {"versioned_ensembl_gene_id":"ENSG00000232891.1","gene_symbol":"AL450344.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":150600834,"end":150605850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275075.1","gene_symbol":"AC244015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144168752,"end":144168850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213089.4","gene_symbol":"PDCL3P5","gene_name":"phosducin-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44506]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644850","summary":null,"start":150827663,"end":150828384,"strand":1,"description":"phosducin-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44506]"}, {"versioned_ensembl_gene_id":"ENSG00000260316.2","gene_symbol":"AL008727.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":898967,"end":905224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230432.1","gene_symbol":"AC114803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219299002,"end":219304130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266648.1","gene_symbol":"SETP3","gene_name":"SET pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31115]","synonyms":"SETP13","biotype":"processed_pseudogene","ncbi_id":"619349","summary":null,"start":58476138,"end":58476950,"strand":-1,"description":"SET pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31115]"}, {"versioned_ensembl_gene_id":"ENSG00000275767.1","gene_symbol":"AC244015.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144179777,"end":144211729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259070.5","gene_symbol":"LINC00639","gene_name":"long intergenic non-protein coding RNA 639 [Source:HGNC Symbol;Acc:HGNC:27502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283547","summary":null,"start":38749339,"end":38948273,"strand":-1,"description":"long intergenic non-protein coding RNA 639 [Source:HGNC Symbol;Acc:HGNC:27502]"}, {"versioned_ensembl_gene_id":"ENSG00000260807.6","gene_symbol":"AC009041.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":975761,"end":981596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158813.17","gene_symbol":"EDA","gene_name":"ectodysplasin A [Source:HGNC Symbol;Acc:HGNC:3157]","synonyms":"EDA-A1,ED1-A2,ED1-A1,ED1,XLHED,XHED,ODT1,HED,EDA2,EDA1,EDA-A2","biotype":"protein_coding","ncbi_id":"1896","summary":"The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":69616067,"end":70039469,"strand":1,"description":"ectodysplasin A [Source:HGNC Symbol;Acc:HGNC:3157]"}, {"versioned_ensembl_gene_id":"ENSG00000165716.10","gene_symbol":"FAM69B","gene_name":"family with sequence similarity 69 member B [Source:HGNC Symbol;Acc:HGNC:28290]","synonyms":"MGC20262,C9orf136","biotype":"protein_coding","ncbi_id":"138311","summary":"This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011]","start":136712570,"end":136724050,"strand":1,"description":"family with sequence similarity 69 member B [Source:HGNC Symbol;Acc:HGNC:28290]"}, {"versioned_ensembl_gene_id":"ENSG00000054356.13","gene_symbol":"PTPRN","gene_name":"protein tyrosine phosphatase, receptor type N [Source:HGNC Symbol;Acc:HGNC:9676]","synonyms":"IA-2","biotype":"protein_coding","ncbi_id":"5798","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single catalytic domain, and thus represents a receptor-type PTP. This PTP was found to be an autoantigen that is reactive with insulin-dependent diabetes mellitus (IDDM) patient sera, and thus may be a potential target of autoimmunity in diabetes mellitus. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]","start":219289623,"end":219309648,"strand":-1,"description":"protein tyrosine phosphatase, receptor type N [Source:HGNC Symbol;Acc:HGNC:9676]"}, {"versioned_ensembl_gene_id":"ENSG00000225839.2","gene_symbol":"TRMT2B-AS1","gene_name":"TRMT2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41116]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"106481789","summary":null,"start":101043564,"end":101094476,"strand":-1,"description":"TRMT2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41116]"}, {"versioned_ensembl_gene_id":"ENSG00000177459.10","gene_symbol":"ERICH5","gene_name":"glutamate rich 5 [Source:HGNC Symbol;Acc:HGNC:26823]","synonyms":"FLJ39553,C8orf47","biotype":"protein_coding","ncbi_id":"203111","summary":null,"start":98064311,"end":98093610,"strand":1,"description":"glutamate rich 5 [Source:HGNC Symbol;Acc:HGNC:26823]"}, {"versioned_ensembl_gene_id":"ENSG00000232527.7","gene_symbol":"AC245595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144227030,"end":144250288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078269.14","gene_symbol":"SYNJ2","gene_name":"synaptojanin 2 [Source:HGNC Symbol;Acc:HGNC:11504]","synonyms":"INPP5H","biotype":"protein_coding","ncbi_id":"8871","summary":"The gene is a member of the inositol-polyphosphate 5-phosphatase family. The encoded protein interacts with the ras-related C3 botulinum toxin substrate 1, which causes translocation of the encoded protein to the plasma membrane where it inhibits clathrin-mediated endocytosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":157981887,"end":158099176,"strand":1,"description":"synaptojanin 2 [Source:HGNC Symbol;Acc:HGNC:11504]"}, {"versioned_ensembl_gene_id":"ENSG00000232723.1","gene_symbol":"AC013399.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121309995,"end":121310412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236117.1","gene_symbol":"LINC01639","gene_name":"long intergenic non-protein coding RNA 1639 [Source:HGNC Symbol;Acc:HGNC:52426]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373054","summary":null,"start":43400331,"end":43409681,"strand":1,"description":"long intergenic non-protein coding RNA 1639 [Source:HGNC Symbol;Acc:HGNC:52426]"}, {"versioned_ensembl_gene_id":"ENSG00000230081.2","gene_symbol":"HSPE1P28","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49347]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171420","summary":null,"start":112280978,"end":112281335,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49347]"}, {"versioned_ensembl_gene_id":"ENSG00000272815.1","gene_symbol":"AC098850.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16788057,"end":16816540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251147.1","gene_symbol":"AC084871.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184910889,"end":184911352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119314.15","gene_symbol":"PTBP3","gene_name":"polypyrimidine tract binding protein 3 [Source:HGNC Symbol;Acc:HGNC:10253]","synonyms":"ROD1,DKFZp781I1117","biotype":"protein_coding","ncbi_id":"9991","summary":"The protein encoded by this gene binds RNA and is a regulator of cell differentiation. The encoded protein preferentially binds to poly(G) and poly(U) sequences in vitro. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":112217716,"end":112333667,"strand":-1,"description":"polypyrimidine tract binding protein 3 [Source:HGNC Symbol;Acc:HGNC:10253]"}, {"versioned_ensembl_gene_id":"ENSG00000188933.14","gene_symbol":"USP32P1","gene_name":"ubiquitin specific peptidase 32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43570]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"162632","summary":null,"start":16786489,"end":16804455,"strand":1,"description":"ubiquitin specific peptidase 32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43570]"}, {"versioned_ensembl_gene_id":"ENSG00000102606.17","gene_symbol":"ARHGEF7","gene_name":"Rho guanine nucleotide exchange factor 7 [Source:HGNC Symbol;Acc:HGNC:15607]","synonyms":"P85,P50BP,P50,Nbla10314,KIAA0142,DKFZp761K1021,DKFZp686C12170,COOL1,BETA-PIX,PIXB,PAK3,P85SPR,P85COOL1","biotype":"protein_coding","ncbi_id":"8874","summary":"This gene encodes a protein that belongs to a family of cytoplasmic proteins that activate the Ras-like family of Rho proteins by exchanging bound GDP for GTP. It forms a complex with the small GTP binding protein Rac1 and recruits Rac1 to membrane ruffles and to focal adhesions. Multiple alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Mar 2016]","start":111114559,"end":111305737,"strand":1,"description":"Rho guanine nucleotide exchange factor 7 [Source:HGNC Symbol;Acc:HGNC:15607]"}, {"versioned_ensembl_gene_id":"ENSG00000108389.9","gene_symbol":"MTMR4","gene_name":"myotubularin related protein 4 [Source:HGNC Symbol;Acc:HGNC:7452]","synonyms":"ZFYVE11,KIAA0647","biotype":"protein_coding","ncbi_id":"9110","summary":null,"start":58489529,"end":58517905,"strand":-1,"description":"myotubularin related protein 4 [Source:HGNC Symbol;Acc:HGNC:7452]"}, {"versioned_ensembl_gene_id":"ENSG00000228595.1","gene_symbol":"PAICSP2","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8589]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780815","summary":null,"start":91611343,"end":91612492,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8589]"}, {"versioned_ensembl_gene_id":"ENSG00000228974.5","gene_symbol":"AC006483.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5560743,"end":5561055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258680.2","gene_symbol":"AL132994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38835389,"end":38835788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169071.14","gene_symbol":"ROR2","gene_name":"receptor tyrosine kinase like orphan receptor 2 [Source:HGNC Symbol;Acc:HGNC:10257]","synonyms":"NTRKR2,BDB1,BDB","biotype":"protein_coding","ncbi_id":"4920","summary":"The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]","start":91563091,"end":91950162,"strand":-1,"description":"receptor tyrosine kinase like orphan receptor 2 [Source:HGNC Symbol;Acc:HGNC:10257]"}, {"versioned_ensembl_gene_id":"ENSG00000226619.1","gene_symbol":"AL137001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19027837,"end":19028701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277109.1","gene_symbol":"AL935212.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61581813,"end":61582675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272719.1","gene_symbol":"AC006483.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5556731,"end":5557245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187721.8","gene_symbol":"GTF2IP3","gene_name":"general transcription factor IIi pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42640]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645686","summary":null,"start":19026001,"end":19032626,"strand":-1,"description":"general transcription factor IIi pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42640]"}, {"versioned_ensembl_gene_id":"ENSG00000268030.1","gene_symbol":"AC005253.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18557775,"end":18561560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233016.6","gene_symbol":"SNHG7","gene_name":"small nucleolar RNA host gene 7 [Source:HGNC Symbol;Acc:HGNC:28254]","synonyms":"MGC16037,NCRNA00061","biotype":"antisense_RNA","ncbi_id":"84973","summary":null,"start":136721366,"end":136728184,"strand":-1,"description":"small nucleolar RNA host gene 7 [Source:HGNC Symbol;Acc:HGNC:28254]"}, {"versioned_ensembl_gene_id":"ENSG00000281870.1","gene_symbol":"AC208814.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30406695,"end":30413531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231248.2","gene_symbol":"AL935212.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61615876,"end":61627683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105700.10","gene_symbol":"KXD1","gene_name":"KxDL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28420]","synonyms":"MGC2749,KXDL,FLJ25480,C19orf50,BORCS4","biotype":"protein_coding","ncbi_id":"79036","summary":null,"start":18557762,"end":18569387,"strand":1,"description":"KxDL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28420]"}, {"versioned_ensembl_gene_id":"ENSG00000236811.1","gene_symbol":"GAPDHP2","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16577]","synonyms":"dJ585I14.1,GAPDP2","biotype":"processed_pseudogene","ncbi_id":"170516","summary":null,"start":13392677,"end":13393674,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16577]"}, {"versioned_ensembl_gene_id":"ENSG00000118017.3","gene_symbol":"A4GNT","gene_name":"alpha-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:17968]","synonyms":"alpha4GnT","biotype":"protein_coding","ncbi_id":"51146","summary":"This gene encodes a protein from the glycosyltransferase 32 family. The enzyme catalyzes the transfer of N-acetylglucosamine (GlcNAc) to core 2 branched O-glycans. It forms a unique glycan, GlcNAcalpha1-->4Galbeta-->R and is largely associated with the Golgi apparatus membrane. [provided by RefSeq, Jul 2008]","start":138123718,"end":138132387,"strand":-1,"description":"alpha-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:17968]"}, {"versioned_ensembl_gene_id":"ENSG00000276586.1","gene_symbol":"AL356102.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62397645,"end":62397916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219986.2","gene_symbol":"BTF3P7","gene_name":"basic transcription factor 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38569]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652960","summary":null,"start":6794915,"end":6795402,"strand":-1,"description":"basic transcription factor 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38569]"}, {"versioned_ensembl_gene_id":"ENSG00000253106.1","gene_symbol":"AC090198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124488510,"end":124491643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219507.4","gene_symbol":"FTH1P8","gene_name":"ferritin heavy chain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3995]","synonyms":"FTHL8","biotype":"processed_pseudogene","ncbi_id":"2501","summary":null,"start":148052233,"end":148052746,"strand":1,"description":"ferritin heavy chain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3995]"}, {"versioned_ensembl_gene_id":"ENSG00000197976.11","gene_symbol":"AKAP17A","gene_name":"A-kinase anchoring protein 17A [Source:HGNC Symbol;Acc:HGNC:18783]","synonyms":"XE7Y,XE7,SFRS17A,MGC39904,DXYS155E,CXYorf3,CCDC133,721P","biotype":"protein_coding","ncbi_id":"8227","summary":"This locus encodes a protein kinase A anchoring protein. The encoded protein is part of the spliceosome complex and is involved in the regulation of alternate splicing in some mRNA precursors. Alternatively spliced transcript variants have been identified for this gene.[provided by RefSeq, Sep 2010]","start":1591593,"end":1602514,"strand":1,"description":"A-kinase anchoring protein 17A [Source:HGNC Symbol;Acc:HGNC:18783]"}, {"versioned_ensembl_gene_id":"ENSG00000271465.1","gene_symbol":"SQSTM1P1","gene_name":"sequestosome 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480677","summary":null,"start":62406058,"end":62406916,"strand":-1,"description":"sequestosome 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49099]"}, {"versioned_ensembl_gene_id":"ENSG00000147687.18","gene_symbol":"TATDN1","gene_name":"TatD DNase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24220]","synonyms":"CDA11","biotype":"protein_coding","ncbi_id":"83940","summary":null,"start":124488485,"end":124539458,"strand":-1,"description":"TatD DNase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24220]"}, {"versioned_ensembl_gene_id":"ENSG00000231061.1","gene_symbol":"LINC00395","gene_name":"long intergenic non-protein coding RNA 395 [Source:HGNC Symbol;Acc:HGNC:42723]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874157","summary":null,"start":63667681,"end":63738018,"strand":-1,"description":"long intergenic non-protein coding RNA 395 [Source:HGNC Symbol;Acc:HGNC:42723]"}, {"versioned_ensembl_gene_id":"ENSG00000281562.1","gene_symbol":"AC233280.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284740.1","gene_symbol":"AL645728.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1503250,"end":1509452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100399.15","gene_symbol":"CHADL","gene_name":"chondroadherin like [Source:HGNC Symbol;Acc:HGNC:25165]","synonyms":"SLRR4B","biotype":"protein_coding","ncbi_id":"150356","summary":null,"start":41229510,"end":41240934,"strand":-1,"description":"chondroadherin like [Source:HGNC Symbol;Acc:HGNC:25165]"}, {"versioned_ensembl_gene_id":"ENSG00000100029.17","gene_symbol":"PES1","gene_name":"pescadillo ribosomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8848]","synonyms":"PES,NOP7","biotype":"protein_coding","ncbi_id":"23481","summary":"This gene encodes a nuclear protein that contains a breast cancer associated gene 1 (BRCA1) C-terminal interaction domain. The encoded protein interacts with BOP1 and WDR12 to form the PeBoW complex, which plays a critical role in cell proliferation via pre-rRNA processing and 60S ribosomal subunit maturation. Expression of this gene may play an important role in breast cancer proliferation and tumorigenicity. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Pseudogenes of this gene are located on the long arm of chromosome 4 and the short arm of chromosome 9. [provided by RefSeq, Aug 2011]","start":30576625,"end":30607083,"strand":-1,"description":"pescadillo ribosomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8848]"}, {"versioned_ensembl_gene_id":"ENSG00000226057.6","gene_symbol":"PHF2P2","gene_name":"PHD finger protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38808]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100873793","summary":null,"start":18946755,"end":19062718,"strand":-1,"description":"PHD finger protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38808]"}, {"versioned_ensembl_gene_id":"ENSG00000255004.1","gene_symbol":"AL133330.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35281813,"end":35286009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255542.1","gene_symbol":"AC090625.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35419057,"end":35421002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169851.15","gene_symbol":"PCDH7","gene_name":"protocadherin 7 [Source:HGNC Symbol;Acc:HGNC:8659]","synonyms":"PPP1R120,BH-Pcdh","biotype":"protein_coding","ncbi_id":"5099","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The gene encodes a protein with an extracellular domain containing 7 cadherin repeats. The gene product is an integral membrane protein that is thought to function in cell-cell recognition and adhesion. Alternative splicing yields isoforms with unique cytoplasmic tails. [provided by RefSeq, Jul 2008]","start":30720415,"end":31146805,"strand":1,"description":"protocadherin 7 [Source:HGNC Symbol;Acc:HGNC:8659]"}, {"versioned_ensembl_gene_id":"ENSG00000215380.2","gene_symbol":"AC090625.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35374265,"end":35374474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268279.4","gene_symbol":"AC090004.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14135217,"end":14148252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229375.1","gene_symbol":"USP24P1","gene_name":"ubiquitin specific peptidase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42014]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874248","summary":null,"start":19015487,"end":19019336,"strand":-1,"description":"ubiquitin specific peptidase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42014]"}, {"versioned_ensembl_gene_id":"ENSG00000174963.17","gene_symbol":"ZIC4","gene_name":"Zic family member 4 [Source:HGNC Symbol;Acc:HGNC:20393]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84107","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. Members of this family are important during development, and have been associated with X-linked visceral heterotaxy and holoprosencephaly type 5. This gene is closely linked to the gene encoding zinc finger protein of the cerebellum 1, a related family member on chromosome 3. Heterozygous deletion of these linked genes is involved in Dandy-Walker malformation, which is a congenital cerebellar malformation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Dec 2009]","start":147386046,"end":147406860,"strand":-1,"description":"Zic family member 4 [Source:HGNC Symbol;Acc:HGNC:20393]"}, {"versioned_ensembl_gene_id":"ENSG00000223447.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33271325,"end":33271451,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000228242.6","gene_symbol":"AC093495.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14144637,"end":14165978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233229.1","gene_symbol":"CNOT7P1","gene_name":"CCR4-NOT transcription complex subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421338","summary":null,"start":69937166,"end":69938017,"strand":-1,"description":"CCR4-NOT transcription complex subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44248]"}, {"versioned_ensembl_gene_id":"ENSG00000175467.14","gene_symbol":"SART1","gene_name":"SART1, U4/U6.U5 tri-snRNP-associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10538]","synonyms":"Snu66,SNRNP110,HAF,Ara1","biotype":"protein_coding","ncbi_id":"9092","summary":"This gene encodes two proteins, the SART1(800) protein expressed in the nucleus of the majority of proliferating cells, and the SART1(259) protein expressed in the cytosol of epithelial cancers. The SART1(259) protein is translated by the mechanism of -1 frameshifting during posttranscriptional regulation; its full-length sequence is not published yet. The two encoded proteins are thought to be involved in the regulation of proliferation. Both proteins have tumor-rejection antigens. The SART1(259) protein possesses tumor epitopes capable of inducing HLA-A2402-restricted cytotoxic T lymphocytes in cancer patients. This SART1(259) antigen may be useful in specific immunotherapy for cancer patients and may serve as a paradigmatic tool for the diagnosis and treatment of patients with atopy. The SART1(259) protein is found to be essential for the recruitment of the tri-snRNP to the pre-spliceosome in the spliceosome assembly pathway. [provided by RefSeq, Jul 2008]","start":65961689,"end":65979828,"strand":1,"description":"SART1, U4/U6.U5 tri-snRNP-associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10538]"}, {"versioned_ensembl_gene_id":"ENSG00000254337.1","gene_symbol":"AC083967.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68848742,"end":68852763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267669.1","gene_symbol":"AC098847.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":59821040,"end":59825261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154114.12","gene_symbol":"TBCEL","gene_name":"tubulin folding cofactor E like [Source:HGNC Symbol;Acc:HGNC:28115]","synonyms":"MGC10233,LRRC35","biotype":"protein_coding","ncbi_id":"219899","summary":null,"start":121024072,"end":121090775,"strand":1,"description":"tubulin folding cofactor E like [Source:HGNC Symbol;Acc:HGNC:28115]"}, {"versioned_ensembl_gene_id":"ENSG00000126550.8","gene_symbol":"HTN1","gene_name":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]","synonyms":"HIS1","biotype":"protein_coding","ncbi_id":"3346","summary":"This gene encodes a member of the histatin family of small, histidine-rich, cationic proteins. They function as antimicrobial peptides and are important components of the innate immune system. Histatins are found in saliva and exhibit antibacterial, antifungal activities and function in wound healing. [provided by RefSeq, Aug 2014]","start":70050402,"end":70058845,"strand":1,"description":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]"}, {"versioned_ensembl_gene_id":"ENSG00000198586.13","gene_symbol":"TLK1","gene_name":"tousled like kinase 1 [Source:HGNC Symbol;Acc:HGNC:11841]","synonyms":"PKU-BETA,KIAA0137","biotype":"protein_coding","ncbi_id":"9874","summary":"The protein encoded by this gene is a serine/threonine kinase that may be involved in the regulation of chromatin assembly. The encoded protein is only active when it is phosphorylated, and this phosphorylation is cell cycle-dependent, with the maximal activity of this protein coming during S phase. The catalytic activity of this protein is diminished by DNA damage and by blockage of DNA replication. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":170990823,"end":171231314,"strand":-1,"description":"tousled like kinase 1 [Source:HGNC Symbol;Acc:HGNC:11841]"}, {"versioned_ensembl_gene_id":"ENSG00000274052.1","gene_symbol":"OR7E156P","gene_name":"olfactory receptor family 7 subfamily E member 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:31311]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"283491","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":63742341,"end":63742804,"strand":1,"description":"olfactory receptor family 7 subfamily E member 156 pseudogene [Source:HGNC Symbol;Acc:HGNC:31311]"}, {"versioned_ensembl_gene_id":"ENSG00000281564.1","gene_symbol":"AC233280.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237378.2","gene_symbol":"AL445989.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63746741,"end":63751080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142949.16","gene_symbol":"PTPRF","gene_name":"protein tyrosine phosphatase, receptor type F [Source:HGNC Symbol;Acc:HGNC:9670]","synonyms":"LAR","biotype":"protein_coding","ncbi_id":"5792","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains three Ig-like domains, and nine non-Ig like domains similar to that of neural-cell adhesion molecule. This PTP was shown to function in the regulation of epithelial cell-cell contacts at adherents junctions, as well as in the control of beta-catenin signaling. An increased expression level of this protein was found in the insulin-responsive tissue of obese, insulin-resistant individuals, and may contribute to the pathogenesis of insulin resistance. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]","start":43525187,"end":43623666,"strand":1,"description":"protein tyrosine phosphatase, receptor type F [Source:HGNC Symbol;Acc:HGNC:9670]"}, {"versioned_ensembl_gene_id":"ENSG00000141682.11","gene_symbol":"PMAIP1","gene_name":"phorbol-12-myristate-13-acetate-induced protein 1 [Source:HGNC Symbol;Acc:HGNC:9108]","synonyms":"APR,NOXA","biotype":"protein_coding","ncbi_id":"5366","summary":"This gene belongs to a pro-apoptotic subfamily within the BCL-2 protein family, referred to as the BCL-2 homology domain 3 (BH3)-only subfamily, which determine whether a cell commits to apoptosis. In response to death-inducing stimuli, BH3-only members inhibit the anti-apoptotic BCL-2 family members, which under steady-state conditions keep the multi-BH domain proteins BAX and BAK, in an inactive state. [provided by RefSeq, Aug 2020]","start":59899948,"end":59904306,"strand":1,"description":"phorbol-12-myristate-13-acetate-induced protein 1 [Source:HGNC Symbol;Acc:HGNC:9108]"}, {"versioned_ensembl_gene_id":"ENSG00000250624.1","gene_symbol":"MTCYBP43","gene_name":"mitochondrially encoded cytochrome b pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52311]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729119","summary":null,"start":30884443,"end":30885182,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52311]"}, {"versioned_ensembl_gene_id":"ENSG00000249678.1","gene_symbol":"AC097716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30776257,"end":30793970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261442.1","gene_symbol":"AC023830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4634329,"end":4640623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264892.1","gene_symbol":"NOS2P4","gene_name":"nitric oxide synthase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266619","summary":null,"start":16812447,"end":16812651,"strand":1,"description":"nitric oxide synthase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50720]"}, {"versioned_ensembl_gene_id":"ENSG00000228669.1","gene_symbol":"LINC00448","gene_name":"long intergenic non-protein coding RNA 448 [Source:HGNC Symbol;Acc:HGNC:42785]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874176","summary":null,"start":62672285,"end":62732359,"strand":-1,"description":"long intergenic non-protein coding RNA 448 [Source:HGNC Symbol;Acc:HGNC:42785]"}, {"versioned_ensembl_gene_id":"ENSG00000010244.18","gene_symbol":"ZNF207","gene_name":"zinc finger protein 207 [Source:HGNC Symbol;Acc:HGNC:12998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7756","summary":null,"start":32350117,"end":32381886,"strand":1,"description":"zinc finger protein 207 [Source:HGNC Symbol;Acc:HGNC:12998]"}, {"versioned_ensembl_gene_id":"ENSG00000146039.10","gene_symbol":"SLC17A4","gene_name":"solute carrier family 17 member 4 [Source:HGNC Symbol;Acc:HGNC:10932]","synonyms":"KIAA2138","biotype":"protein_coding","ncbi_id":"10050","summary":"Phosphate homeostasis is maintained by regulating intake, intestinal absorption, bone deposition and resorption, and renal excretion of phosphate. The central molecule in the control of phosphate excretion from the kidney is the sodium/phosphate cotransporter NPT1 (SLC17A1; MIM 182308), which is located in the renal proximal tubule. NPT1 uses the transmembrane electrochemical potential gradient of sodium to transport phosphate across the cell membrane. SLC17A4 is a similar sodium/phosphate cotransporter in the intestinal mucosa that plays an important role in the absorption of phosphate from the intestine (summary by Shibui et al., 1999 [PubMed 10319585]).[supplied by OMIM, Feb 2011]","start":25754699,"end":25781191,"strand":1,"description":"solute carrier family 17 member 4 [Source:HGNC Symbol;Acc:HGNC:10932]"}, {"versioned_ensembl_gene_id":"ENSG00000266302.6","gene_symbol":"AC098850.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16690261,"end":16804453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102858.12","gene_symbol":"MGRN1","gene_name":"mahogunin ring finger 1 [Source:HGNC Symbol;Acc:HGNC:20254]","synonyms":"RNF156,KIAA0544","biotype":"protein_coding","ncbi_id":"23295","summary":"Mahogunin (MGRN1) is a C3HC4 RING-containing protein with E3 ubiquitin ligase activity in vitro.[supplied by OMIM, Apr 2004]","start":4616493,"end":4690974,"strand":1,"description":"mahogunin ring finger 1 [Source:HGNC Symbol;Acc:HGNC:20254]"}, {"versioned_ensembl_gene_id":"ENSG00000239593.1","gene_symbol":"AL513122.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121279863,"end":121282730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233467.2","gene_symbol":"U40455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148198014,"end":148198878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119396.10","gene_symbol":"RAB14","gene_name":"RAB14, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16524]","synonyms":"RAB-14,FBP","biotype":"protein_coding","ncbi_id":"51552","summary":"RAB14 belongs to the large RAB family of low molecular mass GTPases that are involved in intracellular membrane trafficking. These proteins act as molecular switches that flip between an inactive GDP-bound state and an active GTP-bound state in which they recruit downstream effector proteins onto membranes (Junutula et al., 2004 [PubMed 15004230]).[supplied by OMIM, Mar 2009]","start":121178137,"end":121223014,"strand":-1,"description":"RAB14, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16524]"}, {"versioned_ensembl_gene_id":"ENSG00000280892.1","gene_symbol":"AL161638.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30414392,"end":30416755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259928.1","gene_symbol":"AC011840.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30564057,"end":30565576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176970.8","gene_symbol":"RPL7L1P11","gene_name":"ribosomal protein L7 like 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347509","summary":null,"start":148464708,"end":148465428,"strand":1,"description":"ribosomal protein L7 like 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39493]"}, {"versioned_ensembl_gene_id":"ENSG00000249054.2","gene_symbol":"FAM138D","gene_name":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]","synonyms":"F379,F379","biotype":"lincRNA","ncbi_id":"677784","summary":null,"start":36602,"end":38133,"strand":-1,"description":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]"}, {"versioned_ensembl_gene_id":"ENSG00000264673.1","gene_symbol":"AC098850.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16788248,"end":16789234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273550.1","gene_symbol":"AL354810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63034992,"end":63097797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282718.1","gene_symbol":"AC104333.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212916787,"end":212917577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198830.10","gene_symbol":"HMGN2","gene_name":"high mobility group nucleosomal binding domain 2 [Source:HGNC Symbol;Acc:HGNC:4986]","synonyms":"HMG17","biotype":"protein_coding","ncbi_id":"3151","summary":"The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014]","start":26472450,"end":26475972,"strand":1,"description":"high mobility group nucleosomal binding domain 2 [Source:HGNC Symbol;Acc:HGNC:4986]"}, {"versioned_ensembl_gene_id":"ENSG00000237741.1","gene_symbol":"AC002368.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148498113,"end":148500615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170160.17","gene_symbol":"CCDC144A","gene_name":"coiled-coil domain containing 144A [Source:HGNC Symbol;Acc:HGNC:29072]","synonyms":"KIAA0565,FLJ43983","biotype":"protein_coding","ncbi_id":"9720","summary":null,"start":16689537,"end":16777881,"strand":1,"description":"coiled-coil domain containing 144A [Source:HGNC Symbol;Acc:HGNC:29072]"}, {"versioned_ensembl_gene_id":"ENSG00000231870.4","gene_symbol":"KRT17P3","gene_name":"keratin 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33697]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729682","summary":null,"start":30567700,"end":30571748,"strand":-1,"description":"keratin 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33697]"}, {"versioned_ensembl_gene_id":"ENSG00000227564.2","gene_symbol":"LINC00376","gene_name":"long intergenic non-protein coding RNA 376 [Source:HGNC Symbol;Acc:HGNC:42701]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355293","summary":null,"start":63183101,"end":63328094,"strand":-1,"description":"long intergenic non-protein coding RNA 376 [Source:HGNC Symbol;Acc:HGNC:42701]"}, {"versioned_ensembl_gene_id":"ENSG00000281104.1","gene_symbol":"AL161638.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30420942,"end":30426225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281188.1","gene_symbol":"AC233280.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195639990,"end":195640460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235590.7","gene_symbol":"GNAS-AS1","gene_name":"GNAS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24872]","synonyms":"GNASAS,GNAS1AS,GNAS-AS,SANG,NESPAS,NESP-AS,NCRNA00075","biotype":"antisense_RNA","ncbi_id":"149775","summary":"This gene produces a paternally-imprinted antisense RNA transcript that helps regulate the GNAS complex locus, which encodes the alpha subunit of the stimulatory G protein. Defects in this gene are a cause of pseudohypoparathyroidism type Ib.[provided by RefSeq, Jun 2010]","start":58818919,"end":58850903,"strand":-1,"description":"GNAS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24872]"}, {"versioned_ensembl_gene_id":"ENSG00000282536.1","gene_symbol":"LINC00328-2P","gene_name":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]","synonyms":"NCRNA00328B,NCRNA00328-2P","biotype":"processed_pseudogene","ncbi_id":"100874404","summary":null,"start":18809830,"end":18810048,"strand":1,"description":"long intergenic non-protein coding RNA 328-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42027]"}, {"versioned_ensembl_gene_id":"ENSG00000225806.7","gene_symbol":"AL121917.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58863528,"end":58888809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224027.1","gene_symbol":"AL133456.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27563839,"end":27573573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235513.1","gene_symbol":"AL035681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41209122,"end":41217627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227838.1","gene_symbol":"AL121885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27676559,"end":27714970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231495.1","gene_symbol":"AL121885.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27707580,"end":27709931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099937.10","gene_symbol":"SERPIND1","gene_name":"serpin family D member 1 [Source:HGNC Symbol;Acc:HGNC:4838]","synonyms":"HLS2,HCF2,HC2,HC-II,D22S673","biotype":"protein_coding","ncbi_id":"3053","summary":"This gene belongs to the serpin gene superfamily. Serpins play roles in many processes including inflammation, blood clotting, and cancer metastasis. Members of this family have highly conserved secondary structures with a reactive center loop that interacts with the protease active site to inhibit protease activity. This gene encodes a plasma serine protease that functions as a thrombin and chymotrypsin inhibitor. The protein is activated by heparin, dermatan sulfate, and glycosaminoglycans. Allelic variations in this gene are associated with heparin cofactor II deficiency. [provided by RefSeq, Jul 2015]","start":20773879,"end":20787720,"strand":1,"description":"serpin family D member 1 [Source:HGNC Symbol;Acc:HGNC:4838]"}, {"versioned_ensembl_gene_id":"ENSG00000274829.4","gene_symbol":"PARN","gene_name":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]","synonyms":"DAN","biotype":"protein_coding","ncbi_id":"5073","summary":"The protein encoded by this gene is a 3'-exoribonuclease, with similarity to the RNase D family of 3'-exonucleases. It prefers poly(A) as the substrate, hence, efficiently degrades poly(A) tails of mRNAs. Exonucleolytic degradation of the poly(A) tail is often the first step in the decay of eukaryotic mRNAs. This protein is also involved in silencing of certain maternal mRNAs during oocyte maturation and early embryonic development, as well as in nonsense-mediated decay (NMD) of mRNAs that contain premature stop codons. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":14435701,"end":14632727,"strand":-1,"description":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]"}, {"versioned_ensembl_gene_id":"ENSG00000226169.1","gene_symbol":"AL121885.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27716480,"end":27721677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238170.1","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478955","summary":null,"start":32025384,"end":32028913,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000254479.1","gene_symbol":"SLC25A1P1","gene_name":"solute carrier family 25 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43845]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131457","summary":null,"start":85934737,"end":85935663,"strand":1,"description":"solute carrier family 25 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43845]"}, {"versioned_ensembl_gene_id":"ENSG00000267291.1","gene_symbol":"AC008649.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38596346,"end":38601694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087460.24","gene_symbol":"GNAS","gene_name":"GNAS complex locus [Source:HGNC Symbol;Acc:HGNC:4392]","synonyms":"NESP55,NESP,GPSA,GNASXL,GNAS1,SgVI,SCG6","biotype":"protein_coding","ncbi_id":"2778","summary":"This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]","start":58839718,"end":58911192,"strand":1,"description":"GNAS complex locus [Source:HGNC Symbol;Acc:HGNC:4392]"}, {"versioned_ensembl_gene_id":"ENSG00000166347.18","gene_symbol":"CYB5A","gene_name":"cytochrome b5 type A [Source:HGNC Symbol;Acc:HGNC:2570]","synonyms":"CYB5","biotype":"protein_coding","ncbi_id":"1528","summary":"The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":74250847,"end":74292016,"strand":-1,"description":"cytochrome b5 type A [Source:HGNC Symbol;Acc:HGNC:2570]"}, {"versioned_ensembl_gene_id":"ENSG00000239393.1","gene_symbol":"AC146507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177346073,"end":177346426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169223.14","gene_symbol":"LMAN2","gene_name":"lectin, mannose binding 2 [Source:HGNC Symbol;Acc:HGNC:16986]","synonyms":"VIP36,GP36B,C5orf8","biotype":"protein_coding","ncbi_id":"10960","summary":"This gene encodes a type I transmembrane lectin that shuttles between the endoplasmic reticulum, the Golgi apparatus and the plasma membrane. The encoded protein binds high mannose type glycoproteins and may facilitate their sorting, trafficking and quality control. [provided by RefSeq, Oct 2008]","start":177331562,"end":177351852,"strand":-1,"description":"lectin, mannose binding 2 [Source:HGNC Symbol;Acc:HGNC:16986]"}, {"versioned_ensembl_gene_id":"ENSG00000125531.6","gene_symbol":"FNDC11","gene_name":"fibronectin type III domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28764]","synonyms":"MGC5356,C20orf195","biotype":"protein_coding","ncbi_id":"79025","summary":null,"start":63547891,"end":63556708,"strand":1,"description":"fibronectin type III domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28764]"}, {"versioned_ensembl_gene_id":"ENSG00000104814.12","gene_symbol":"MAP4K1","gene_name":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]","synonyms":"HPK1","biotype":"protein_coding","ncbi_id":"11184","summary":null,"start":38587641,"end":38618882,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]"}, {"versioned_ensembl_gene_id":"ENSG00000250220.1","gene_symbol":"AC053527.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73259209,"end":73317953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231955.1","gene_symbol":"AC007383.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206115547,"end":206122323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249976.2","gene_symbol":"AC108157.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73337233,"end":73337771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237580.1","gene_symbol":"GCSHP3","gene_name":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100329109","summary":null,"start":206116110,"end":206116500,"strand":-1,"description":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]"}, {"versioned_ensembl_gene_id":"ENSG00000223342.2","gene_symbol":"AL158817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6901022,"end":6918715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271797.1","gene_symbol":"AC008494.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115262505,"end":115263448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250650.1","gene_symbol":"AC093534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117019548,"end":117019679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099940.11","gene_symbol":"SNAP29","gene_name":"synaptosome associated protein 29 [Source:HGNC Symbol;Acc:HGNC:11133]","synonyms":"SNAP-29,CEDNIK","biotype":"protein_coding","ncbi_id":"9342","summary":"This gene, a member of the SNAP25 gene family, encodes a protein involved in multiple membrane trafficking steps. Two other members of this gene family, SNAP23 and SNAP25, encode proteins that bind a syntaxin protein and mediate synaptic vesicle membrane docking and fusion to the plasma membrane. The protein encoded by this gene binds tightly to multiple syntaxins and is localized to intracellular membrane structures rather than to the plasma membrane. While the protein is mostly membrane-bound, a significant fraction of it is found free in the cytoplasm. Use of multiple polyadenylation sites has been noted for this gene. [provided by RefSeq, Jul 2008]","start":20858983,"end":20891218,"strand":1,"description":"synaptosome associated protein 29 [Source:HGNC Symbol;Acc:HGNC:11133]"}, {"versioned_ensembl_gene_id":"ENSG00000023228.13","gene_symbol":"NDUFS1","gene_name":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]","synonyms":"CI-75k","biotype":"protein_coding","ncbi_id":"4719","summary":"The protein encoded by this gene belongs to the complex I 75 kDa subunit family. Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. This protein is the largest subunit of complex I and it is a component of the iron-sulfur (IP) fragment of the enzyme. It may form part of the active site crevice where NADH is oxidized. Mutations in this gene are associated with complex I deficiency. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":206114817,"end":206159603,"strand":-1,"description":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]"}, {"versioned_ensembl_gene_id":"ENSG00000225922.1","gene_symbol":"RPL21P92","gene_name":"ribosomal protein L21 pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:35606]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130400","summary":null,"start":67793770,"end":67794245,"strand":1,"description":"ribosomal protein L21 pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:35606]"}, {"versioned_ensembl_gene_id":"ENSG00000164219.9","gene_symbol":"PGGT1B","gene_name":"protein geranylgeranyltransferase type I subunit beta [Source:HGNC Symbol;Acc:HGNC:8895]","synonyms":"BGGI,GGTI","biotype":"protein_coding","ncbi_id":"5229","summary":"Protein geranylgeranyltransferase type I (GGTase-I) transfers a geranylgeranyl group to the cysteine residue of candidate proteins containing a C-terminal CAAX motif in which 'A' is an aliphatic amino acid and 'X' is leucine (summarized by Zhang et al., 1994 [PubMed 8106351]). The enzyme is composed of a 48-kD alpha subunit (FNTA; MIM 134635) and a 43-kD beta subunit, encoded by the PGGT1B gene. The FNTA gene encodes the alpha subunit for both GGTase-I and the related enzyme farnesyltransferase.[supplied by OMIM, Mar 2010]","start":115204012,"end":115262872,"strand":-1,"description":"protein geranylgeranyltransferase type I subunit beta [Source:HGNC Symbol;Acc:HGNC:8895]"}, {"versioned_ensembl_gene_id":"ENSG00000067225.17","gene_symbol":"PKM","gene_name":"pyruvate kinase, muscle [Source:HGNC Symbol;Acc:HGNC:9021]","synonyms":"THBP1,PKM2,PK3,OIP3","biotype":"protein_coding","ncbi_id":"5315","summary":"This gene encodes a protein involved in glycolysis. The encoded protein is a pyruvate kinase that catalyzes the transfer of a phosphoryl group from phosphoenolpyruvate to ADP, generating ATP and pyruvate. This protein has been shown to interact with thyroid hormone and may mediate cellular metabolic effects induced by thyroid hormones. This protein has been found to bind Opa protein, a bacterial outer membrane protein involved in gonococcal adherence to and invasion of human cells, suggesting a role of this protein in bacterial pathogenesis. Several alternatively spliced transcript variants encoding a few distinct isoforms have been reported. [provided by RefSeq, May 2011]","start":72199029,"end":72231822,"strand":-1,"description":"pyruvate kinase, muscle [Source:HGNC Symbol;Acc:HGNC:9021]"}, {"versioned_ensembl_gene_id":"ENSG00000267066.1","gene_symbol":"AC107990.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59929226,"end":59930330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152223.12","gene_symbol":"EPG5","gene_name":"ectopic P-granules autophagy protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:29331]","synonyms":"KIAA1632,hEPG5","biotype":"protein_coding","ncbi_id":"57724","summary":"This gene encodes a large coiled coil domain-containing protein that functions in autophagy during starvation conditions. Mutations in this gene cause Vici syndrome. [provided by RefSeq, Aug 2015]","start":45847609,"end":45967274,"strand":-1,"description":"ectopic P-granules autophagy protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:29331]"}, {"versioned_ensembl_gene_id":"ENSG00000267497.1","gene_symbol":"NFE2L3P1","gene_name":"nuclear factor, erythroid 2 like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22278]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642996","summary":null,"start":59969438,"end":59971396,"strand":1,"description":"nuclear factor, erythroid 2 like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22278]"}, {"versioned_ensembl_gene_id":"ENSG00000224043.7","gene_symbol":"CCNT2-AS1","gene_name":"CCNT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40130]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129961","summary":null,"start":134735464,"end":134918710,"strand":-1,"description":"CCNT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40130]"}, {"versioned_ensembl_gene_id":"ENSG00000237141.1","gene_symbol":"DNAJC19P1","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45064]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129853","summary":null,"start":67833763,"end":67834081,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45064]"}, {"versioned_ensembl_gene_id":"ENSG00000108176.14","gene_symbol":"DNAJC12","gene_name":"DnaJ heat shock protein family (Hsp40) member C12 [Source:HGNC Symbol;Acc:HGNC:28908]","synonyms":"JDP1","biotype":"protein_coding","ncbi_id":"56521","summary":"This gene encodes a member of a subclass of the HSP40/DnaJ protein family. Members of this family of proteins are associated with complex assembly, protein folding, and export. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":67796665,"end":67838166,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C12 [Source:HGNC Symbol;Acc:HGNC:28908]"}, {"versioned_ensembl_gene_id":"ENSG00000234682.1","gene_symbol":"VDAC2P4","gene_name":"voltage dependent anion channel 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420574","summary":null,"start":134797169,"end":134797879,"strand":1,"description":"voltage dependent anion channel 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51932]"}, {"versioned_ensembl_gene_id":"ENSG00000223955.1","gene_symbol":"MTND6P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38730]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499469","summary":null,"start":8363536,"end":8363959,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38730]"}, {"versioned_ensembl_gene_id":"ENSG00000268983.1","gene_symbol":"AC005253.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18568506,"end":18569375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187094.11","gene_symbol":"CCK","gene_name":"cholecystokinin [Source:HGNC Symbol;Acc:HGNC:1569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"885","summary":"This gene encodes a member of the gastrin/cholecystokinin family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the peptide hormones cholecystokinin-8, -12, -33, and others. The encoded peptides have been shown to regulate gastric acid secretion and food intake. A sulfated form of cholecystokinin-8 may modulate neuronal activity in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":42257825,"end":42266207,"strand":-1,"description":"cholecystokinin [Source:HGNC Symbol;Acc:HGNC:1569]"}, {"versioned_ensembl_gene_id":"ENSG00000228098.1","gene_symbol":"AC110620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134816362,"end":134816589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235079.1","gene_symbol":"ZRANB2-AS1","gene_name":"ZRANB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43594]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132618","summary":null,"start":71048855,"end":71067184,"strand":1,"description":"ZRANB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43594]"}, {"versioned_ensembl_gene_id":"ENSG00000231966.1","gene_symbol":"AL359853.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179829609,"end":179836124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204814.5","gene_symbol":"AL935212.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61659733,"end":61662690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254879.1","gene_symbol":"PTPRJ-AS1","gene_name":"PTPRJ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50634]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104326192","summary":null,"start":48014406,"end":48015855,"strand":-1,"description":"PTPRJ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50634]"}, {"versioned_ensembl_gene_id":"ENSG00000279792.1","gene_symbol":"AC015909.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50362967,"end":50365232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241973.10","gene_symbol":"PI4KA","gene_name":"phosphatidylinositol 4-kinase alpha [Source:HGNC Symbol;Acc:HGNC:8983]","synonyms":"PIK4CA,pi4K230,PI4K-ALPHA","biotype":"protein_coding","ncbi_id":"5297","summary":"This gene encodes a phosphatidylinositol (PI) 4-kinase which catalyzes the first committed step in the biosynthesis of phosphatidylinositol 4,5-bisphosphate. The mammalian PI 4-kinases have been classified into two types, II and III, based on their molecular mass, and modulation by detergent and adenosine. The protein encoded by this gene is a type III enzyme that is not inhibited by adenosine. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2018]","start":20707691,"end":20859417,"strand":-1,"description":"phosphatidylinositol 4-kinase alpha [Source:HGNC Symbol;Acc:HGNC:8983]"}, {"versioned_ensembl_gene_id":"ENSG00000082258.12","gene_symbol":"CCNT2","gene_name":"cyclin T2 [Source:HGNC Symbol;Acc:HGNC:1600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"905","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin and its kinase partner CDK9 were found to be subunits of the transcription elongation factor p-TEFb. The p-TEFb complex containing this cyclin was reported to interact with, and act as a negative regulator of human immunodeficiency virus type 1 (HIV-1) Tat protein. A pseudogene of this gene is found on chromosome 1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]","start":134918235,"end":134959342,"strand":1,"description":"cyclin T2 [Source:HGNC Symbol;Acc:HGNC:1600]"}, {"versioned_ensembl_gene_id":"ENSG00000249203.1","gene_symbol":"LINC02224","gene_name":"long intergenic non-protein coding RNA 2224 [Source:HGNC Symbol;Acc:HGNC:53093]","synonyms":"ENST00000505706,BRCAT107","biotype":"lincRNA","ncbi_id":"102723839","summary":null,"start":44495618,"end":44510282,"strand":-1,"description":"long intergenic non-protein coding RNA 2224 [Source:HGNC Symbol;Acc:HGNC:53093]"}, {"versioned_ensembl_gene_id":"ENSG00000132485.13","gene_symbol":"ZRANB2","gene_name":"zinc finger RANBP2-type containing 2 [Source:HGNC Symbol;Acc:HGNC:13058]","synonyms":"ZNF265,ZIS2,ZIS1,ZIS","biotype":"protein_coding","ncbi_id":"9406","summary":null,"start":71063291,"end":71081297,"strand":-1,"description":"zinc finger RANBP2-type containing 2 [Source:HGNC Symbol;Acc:HGNC:13058]"}, {"versioned_ensembl_gene_id":"ENSG00000250418.1","gene_symbol":"AC093292.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44698431,"end":44700808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161405.16","gene_symbol":"IKZF3","gene_name":"IKAROS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:13178]","synonyms":"ZNFN1A3,Aiolos","biotype":"protein_coding","ncbi_id":"22806","summary":"This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This gene product is a transcription factor that is important in the regulation of B lymphocyte proliferation and differentiation. Both Ikaros and Aiolos can participate in chromatin remodeling. Regulation of gene expression in B lymphocytes by Aiolos is complex as it appears to require the sequential formation of Ikaros homodimers, Ikaros/Aiolos heterodimers, and Aiolos homodimers. Several alternative transcripts encoding different isoforms have been described, as well as some non-protein coding variants. [provided by RefSeq, Apr 2012]","start":39757715,"end":39864188,"strand":-1,"description":"IKAROS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:13178]"}, {"versioned_ensembl_gene_id":"ENSG00000234179.1","gene_symbol":"MTCYBP1","gene_name":"mitochondrially encoded cytochrome b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38729]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499418","summary":null,"start":8364032,"end":8365150,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38729]"}, {"versioned_ensembl_gene_id":"ENSG00000257176.2","gene_symbol":"AC009318.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29280418,"end":29317848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270160.1","gene_symbol":"AP001995.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128614340,"end":128615236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064763.10","gene_symbol":"FAR2","gene_name":"fatty acyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:25531]","synonyms":"SDR10E2,MLSTD1,FLJ10462","biotype":"protein_coding","ncbi_id":"55711","summary":"This gene belongs to the short chain dehydrogenase/reductase superfamily. It encodes a reductase enzyme involved in the first step of wax biosynthesis wherein fatty acids are converted to fatty alcohols. The encoded peroxisomal protein utilizes saturated fatty acids of 16 or 18 carbons as preferred substrates. Alternatively spliced transcript variants have been observed for this gene. Related pseudogenes have been identified on chromosomes 2, 14 and 22. [provided by RefSeq, Nov 2012]","start":29149103,"end":29340980,"strand":1,"description":"fatty acyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:25531]"}, {"versioned_ensembl_gene_id":"ENSG00000240296.1","gene_symbol":"AC245052.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268005,"end":54269045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255465.3","gene_symbol":"AP001995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128615867,"end":128621806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139445.17","gene_symbol":"FOXN4","gene_name":"forkhead box N4 [Source:HGNC Symbol;Acc:HGNC:21399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"121643","summary":"Members of the winged-helix/forkhead family of transcription factors, such as FOXN4, are characterized by a 110-amino acid DNA-binding domain that can fold into a variant of the helix-turn-helix motif consisting of 3 alpha helices flanked by 2 large loops or wings. These transcription factors are involved in a variety of biologic processes as key regulators in development and metabolism (Li et al., 2004 [PubMed 15363391]).[supplied by OMIM, Mar 2008]","start":109277979,"end":109309220,"strand":-1,"description":"forkhead box N4 [Source:HGNC Symbol;Acc:HGNC:21399]"}, {"versioned_ensembl_gene_id":"ENSG00000243495.1","gene_symbol":"GMFBP1","gene_name":"glia maturation factor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499251","summary":null,"start":100665050,"end":100665476,"strand":-1,"description":"glia maturation factor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38654]"}, {"versioned_ensembl_gene_id":"ENSG00000241202.1","gene_symbol":"ZIC4-AS1","gene_name":"ZIC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40920]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873950","summary":null,"start":147386967,"end":147387453,"strand":1,"description":"ZIC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40920]"}, {"versioned_ensembl_gene_id":"ENSG00000152977.9","gene_symbol":"ZIC1","gene_name":"Zic family member 1 [Source:HGNC Symbol;Acc:HGNC:12872]","synonyms":"ZIC,ZNF201","biotype":"protein_coding","ncbi_id":"7545","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. Members of this family are important during development. Aberrant expression of this gene is seen in medulloblastoma, a childhood brain tumor. This gene is closely linked to the gene encoding zinc finger protein of the cerebellum 4, a related family member on chromosome 3. This gene encodes a transcription factor that can bind and transactivate the apolipoprotein E gene. [provided by RefSeq, Jul 2008]","start":147393422,"end":147510293,"strand":1,"description":"Zic family member 1 [Source:HGNC Symbol;Acc:HGNC:12872]"}, {"versioned_ensembl_gene_id":"ENSG00000102891.3","gene_symbol":"MT4","gene_name":"metallothionein 4 [Source:HGNC Symbol;Acc:HGNC:18705]","synonyms":"MTIV","biotype":"protein_coding","ncbi_id":"84560","summary":null,"start":56565049,"end":56568957,"strand":1,"description":"metallothionein 4 [Source:HGNC Symbol;Acc:HGNC:18705]"}, {"versioned_ensembl_gene_id":"ENSG00000144820.7","gene_symbol":"ADGRG7","gene_name":"adhesion G protein-coupled receptor G7 [Source:HGNC Symbol;Acc:HGNC:19241]","synonyms":"GPR128,FLJ14454","biotype":"protein_coding","ncbi_id":"84873","summary":null,"start":100609589,"end":100695479,"strand":1,"description":"adhesion G protein-coupled receptor G7 [Source:HGNC Symbol;Acc:HGNC:19241]"}, {"versioned_ensembl_gene_id":"ENSG00000272549.1","gene_symbol":"LINC02538","gene_name":"long intergenic non-protein coding RNA 2538 [Source:HGNC Symbol;Acc:HGNC:53571]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401286","summary":null,"start":167666840,"end":167679270,"strand":-1,"description":"long intergenic non-protein coding RNA 2538 [Source:HGNC Symbol;Acc:HGNC:53571]"}, {"versioned_ensembl_gene_id":"ENSG00000105707.13","gene_symbol":"HPN","gene_name":"hepsin [Source:HGNC Symbol;Acc:HGNC:5155]","synonyms":"TMPRSS1","biotype":"protein_coding","ncbi_id":"3249","summary":"This gene encodes a type II transmembrane serine protease that may be involved in diverse cellular functions, including blood coagulation and the maintenance of cell morphology. Expression of the encoded protein is associated with the growth and progression of cancers, particularly prostate cancer. The protein is cleaved into a catalytic serine protease chain and a non-catalytic scavenger receptor cysteine-rich chain, which associate via a single disulfide bond. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":35040506,"end":35066571,"strand":1,"description":"hepsin [Source:HGNC Symbol;Acc:HGNC:5155]"}, {"versioned_ensembl_gene_id":"ENSG00000149177.12","gene_symbol":"PTPRJ","gene_name":"protein tyrosine phosphatase, receptor type J [Source:HGNC Symbol;Acc:HGNC:9673]","synonyms":"HPTPeta,DEP1,CD148","biotype":"protein_coding","ncbi_id":"5795","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes, including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region containing five fibronectin type III repeats, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. This protein is present in all hematopoietic lineages, and was shown to negatively regulate T cell receptor signaling possibly through interfering with the phosphorylation of Phospholipase C Gamma 1 and Linker for Activation of T Cells. This protein can also dephosphorylate the PDGF beta receptor, and may be involved in UV-induced signal transduction. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47980558,"end":48170841,"strand":1,"description":"protein tyrosine phosphatase, receptor type J [Source:HGNC Symbol;Acc:HGNC:9673]"}, {"versioned_ensembl_gene_id":"ENSG00000015532.9","gene_symbol":"XYLT2","gene_name":"xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15517]","synonyms":"XT-II,PXYLT2","biotype":"protein_coding","ncbi_id":"64132","summary":"The protein encoded by this gene is an isoform of xylosyltransferase, which belongs to a family of glycosyltransferases. This enzyme transfers xylose from UDP-xylose to specific serine residues of the core protein and initiates the biosynthesis of glycosaminoglycan chains in proteoglycans including chondroitin sulfate, heparan sulfate, heparin and dermatan sulfate. The enzyme activity, which is increased in scleroderma patients, is a diagnostic marker for the determination of sclerotic activity in systemic sclerosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":50346092,"end":50363138,"strand":1,"description":"xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15517]"}, {"versioned_ensembl_gene_id":"ENSG00000272892.1","gene_symbol":"AL133551.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67849525,"end":67850746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229367.1","gene_symbol":"HMGN2P19","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39383]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874466","summary":null,"start":229570532,"end":229570796,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39383]"}, {"versioned_ensembl_gene_id":"ENSG00000267462.1","gene_symbol":"AC090377.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60010281,"end":60014258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260689.2","gene_symbol":"HNRNPA3P11","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48757]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421431","summary":null,"start":57246960,"end":57247893,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48757]"}, {"versioned_ensembl_gene_id":"ENSG00000256704.3","gene_symbol":"SDCCAG3P1","gene_name":"serologically defined colon cancer antigen 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29375]","synonyms":"SDCCAG3L","biotype":"processed_pseudogene","ncbi_id":"388478","summary":null,"start":60009994,"end":60011143,"strand":-1,"description":"serologically defined colon cancer antigen 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29375]"}, {"versioned_ensembl_gene_id":"ENSG00000248162.1","gene_symbol":"AC074198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164725310,"end":164726706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213065.2","gene_symbol":"AL009178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167767083,"end":167768568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275343.1","gene_symbol":"AC010999.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56908312,"end":56908635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225625.4","gene_symbol":"AC090517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56846340,"end":56846605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219932.6","gene_symbol":"RPL12P8","gene_name":"ribosomal protein L12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23735]","synonyms":"bA57G10.3","biotype":"processed_pseudogene","ncbi_id":"645161","summary":null,"start":67874332,"end":67874911,"strand":1,"description":"ribosomal protein L12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23735]"}, {"versioned_ensembl_gene_id":"ENSG00000256686.1","gene_symbol":"AC019209.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25782706,"end":25814171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245008.3","gene_symbol":"AP001122.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128629653,"end":128686922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255725.2","gene_symbol":"TDGP1","gene_name":"thymine-DNA glycosylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49891]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645233","summary":null,"start":25803298,"end":25804526,"strand":1,"description":"thymine-DNA glycosylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49891]"}, {"versioned_ensembl_gene_id":"ENSG00000269155.2","gene_symbol":"AL009178.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167795530,"end":167798248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137871.19","gene_symbol":"ZNF280D","gene_name":"zinc finger protein 280D [Source:HGNC Symbol;Acc:HGNC:25953]","synonyms":"ZNF634,SUHW4,FLJ20086","biotype":"protein_coding","ncbi_id":"54816","summary":null,"start":56630181,"end":56918571,"strand":-1,"description":"zinc finger protein 280D [Source:HGNC Symbol;Acc:HGNC:25953]"}, {"versioned_ensembl_gene_id":"ENSG00000146521.9","gene_symbol":"LINC01558","gene_name":"long intergenic non-protein coding RNA 1558 [Source:HGNC Symbol;Acc:HGNC:21235]","synonyms":"LINC01557,HGC6.2,dJ431P23.4,C6orf123","biotype":"lincRNA","ncbi_id":"26238","summary":null,"start":167784537,"end":167796859,"strand":-1,"description":"long intergenic non-protein coding RNA 1558 [Source:HGNC Symbol;Acc:HGNC:21235]"}, {"versioned_ensembl_gene_id":"ENSG00000256440.1","gene_symbol":"AC019209.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25831416,"end":25834182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151702.16","gene_symbol":"FLI1","gene_name":"Fli-1 proto-oncogene, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3749]","synonyms":"SIC-1,EWSR2","biotype":"protein_coding","ncbi_id":"2313","summary":"This gene encodes a transcription factor containing an ETS DNA-binding domain. The gene can undergo a t(11;22)(q24;q12) translocation with the Ewing sarcoma gene on chromosome 22, which results in a fusion gene that is present in the majority of Ewing sarcoma cases. An acute lymphoblastic leukemia-associated t(4;11)(q21;q23) translocation involving this gene has also been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":128686535,"end":128813267,"strand":1,"description":"Fli-1 proto-oncogene, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3749]"}, {"versioned_ensembl_gene_id":"ENSG00000256256.1","gene_symbol":"AC019209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25882955,"end":25885855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235581.1","gene_symbol":"AC005011.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71942259,"end":71942468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087250.8","gene_symbol":"MT3","gene_name":"metallothionein 3 [Source:HGNC Symbol;Acc:HGNC:7408]","synonyms":"GIF","biotype":"protein_coding","ncbi_id":"4504","summary":"This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions. This gene family member displays tissue-specific expression, and contains a threonine insert near its N-terminus and a glutamate-rich hexapeptide insert near its C-terminus relative to the proteins encoded by other gene family members. It plays an important role in zinc and copper homeostasis, and is induced under hypoxic conditions. The encoded protein is a growth inhibitory factor, and reduced levels of the protein are observed in the brains of individuals with some metal-linked neurodegenerative disorders such as Alzheimer's disease. [provided by RefSeq, Sep 2017]","start":56589074,"end":56591088,"strand":1,"description":"metallothionein 3 [Source:HGNC Symbol;Acc:HGNC:7408]"}, {"versioned_ensembl_gene_id":"ENSG00000276756.4","gene_symbol":"AC245595.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144276484,"end":144305180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264729.1","gene_symbol":"AC022596.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16804627,"end":16805707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228769.1","gene_symbol":"ABCF2P2","gene_name":"ATP binding cassette subfamily F member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48842]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422059","summary":null,"start":72103181,"end":72104209,"strand":1,"description":"ATP binding cassette subfamily F member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48842]"}, {"versioned_ensembl_gene_id":"ENSG00000266129.1","gene_symbol":"SRP68P1","gene_name":"signal recognition particle 68 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30427]","synonyms":"SRPSMCR","biotype":"processed_pseudogene","ncbi_id":"252841","summary":null,"start":16787235,"end":16788141,"strand":-1,"description":"signal recognition particle 68 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30427]"}, {"versioned_ensembl_gene_id":"ENSG00000183166.10","gene_symbol":"CALN1","gene_name":"calneuron 1 [Source:HGNC Symbol;Acc:HGNC:13248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83698","summary":"This gene encodes a protein with high similarity to the calcium-binding proteins of the calmodulin family. The encoded protein contains two EF-hand domains and potential calcium-binding sites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":71779491,"end":72447151,"strand":-1,"description":"calneuron 1 [Source:HGNC Symbol;Acc:HGNC:13248]"}, {"versioned_ensembl_gene_id":"ENSG00000266486.1","gene_symbol":"FAM106CP","gene_name":"family with sequence similarity 106 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38396]","synonyms":"FAM106C","biotype":"processed_pseudogene","ncbi_id":"100129396","summary":null,"start":16788901,"end":16789407,"strand":1,"description":"family with sequence similarity 106 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38396]"}, {"versioned_ensembl_gene_id":"ENSG00000226478.3","gene_symbol":"UPF3AP1","gene_name":"UPF3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30568]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"147226","summary":null,"start":16745636,"end":16746761,"strand":-1,"description":"UPF3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30568]"}, {"versioned_ensembl_gene_id":"ENSG00000175658.4","gene_symbol":"DRD5P2","gene_name":"dopamine receptor D5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1818","summary":null,"start":144274892,"end":144277993,"strand":-1,"description":"dopamine receptor D5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3028]"}, {"versioned_ensembl_gene_id":"ENSG00000135801.9","gene_symbol":"TAF5L","gene_name":"TATA-box binding protein associated factor 5 like [Source:HGNC Symbol;Acc:HGNC:17304]","synonyms":"PAF65B","biotype":"protein_coding","ncbi_id":"27097","summary":"The product of this gene belongs to the WD-repeat TAF5 family of proteins. This gene encodes a protein that is a component of the PCAF histone acetylase complex. The PCAF histone acetylase complex, which is composed of more than 20 polypeptides some of which are TAFs, is required for myogenic transcription and differentiation. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors to facilitate complex assembly and transcription initiation. The encoded protein is structurally similar to one of the histone-like TAFs, TAF5. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":229593111,"end":229626047,"strand":-1,"description":"TATA-box binding protein associated factor 5 like [Source:HGNC Symbol;Acc:HGNC:17304]"}, {"versioned_ensembl_gene_id":"ENSG00000274671.4","gene_symbol":"MARVELD2","gene_name":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]","synonyms":"TRIC,MRVLDC2,FLJ30532,DFNB49","biotype":"protein_coding","ncbi_id":"153562","summary":"The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":69415353,"end":69444141,"strand":1,"description":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]"}, {"versioned_ensembl_gene_id":"ENSG00000271567.1","gene_symbol":"PPIAL4E","gene_name":"peptidylprolyl isomerase A like 4E [Source:HGNC Symbol;Acc:HGNC:33997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730262","summary":null,"start":144372875,"end":144373659,"strand":-1,"description":"peptidylprolyl isomerase A like 4E [Source:HGNC Symbol;Acc:HGNC:33997]"}, {"versioned_ensembl_gene_id":"ENSG00000121486.11","gene_symbol":"TRMT1L","gene_name":"tRNA methyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:16782]","synonyms":"C1orf25","biotype":"protein_coding","ncbi_id":"81627","summary":"This gene encodes a protein that has some similarity to N2,N2-dimethylguanosine tRNA methyltransferase from other organisms. Studies of the mouse ortholog have shown that this protein plays a role in motor coordination and exploratory behavior, and it may also be involved in modulating postnatal neuronal functions. Alternatively spliced transcripts have been identified for this gene. [provided by RefSeq, Jan 2011]","start":185118098,"end":185157072,"strand":-1,"description":"tRNA methyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:16782]"}, {"versioned_ensembl_gene_id":"ENSG00000271439.1","gene_symbol":"AC246785.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144401069,"end":144401355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233586.1","gene_symbol":"AC246785.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144418678,"end":144419190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269425.1","gene_symbol":"AC104521.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4339577,"end":4343491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237343.1","gene_symbol":"AC246785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144418113,"end":144419192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231402.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31287510,"end":31288964,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000248771.5","gene_symbol":"SMIM31","gene_name":"small integral membrane protein 31 [Source:HGNC Symbol;Acc:HGNC:49638]","synonyms":"LINC01207","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":164754064,"end":164803795,"strand":1,"description":"small integral membrane protein 31 [Source:HGNC Symbol;Acc:HGNC:49638]"}, {"versioned_ensembl_gene_id":"ENSG00000178078.11","gene_symbol":"STAP2","gene_name":"signal transducing adaptor family member 2 [Source:HGNC Symbol;Acc:HGNC:30430]","synonyms":"STAP-2,BKS","biotype":"protein_coding","ncbi_id":"55620","summary":"This gene encodes the substrate of breast tumor kinase, an Src-type non-receptor tyrosine kinase. The encoded protein possesses domains and several tyrosine phosphorylation sites characteristic of adaptor proteins that mediate the interactions linking proteins involved in signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":4324043,"end":4342786,"strand":-1,"description":"signal transducing adaptor family member 2 [Source:HGNC Symbol;Acc:HGNC:30430]"}, {"versioned_ensembl_gene_id":"ENSG00000256166.1","gene_symbol":"AL671883.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31293908,"end":31301642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279000.3","gene_symbol":"OR10A6","gene_name":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":7924592,"end":7931268,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]"}, {"versioned_ensembl_gene_id":"ENSG00000163818.16","gene_symbol":"LZTFL1","gene_name":"leucine zipper transcription factor like 1 [Source:HGNC Symbol;Acc:HGNC:6741]","synonyms":"BBS17","biotype":"protein_coding","ncbi_id":"54585","summary":"This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome; a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor; possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. [provided by RefSeq, Aug 2020]","start":45823316,"end":45916042,"strand":-1,"description":"leucine zipper transcription factor like 1 [Source:HGNC Symbol;Acc:HGNC:6741]"}, {"versioned_ensembl_gene_id":"ENSG00000177483.11","gene_symbol":"RBM44","gene_name":"RNA binding motif protein 44 [Source:HGNC Symbol;Acc:HGNC:24756]","synonyms":"FLJ40411","biotype":"protein_coding","ncbi_id":"375316","summary":null,"start":237798389,"end":237842808,"strand":1,"description":"RNA binding motif protein 44 [Source:HGNC Symbol;Acc:HGNC:24756]"}, {"versioned_ensembl_gene_id":"ENSG00000234175.1","gene_symbol":"AL355355.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13139196,"end":13139533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256540.1","gene_symbol":"AC007406.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166856,"end":182399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234745.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31269491,"end":31357188,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000257415.1","gene_symbol":"AC084364.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103503381,"end":103504936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234427.1","gene_symbol":"AL022724.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11810602,"end":11811248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215124.2","gene_symbol":"AMD1P4","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51609]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129761","summary":null,"start":11861626,"end":11862970,"strand":-1,"description":"adenosylmethionine decarboxylase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51609]"}, {"versioned_ensembl_gene_id":"ENSG00000170683.6","gene_symbol":"OR10A3","gene_name":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]","synonyms":"HTPCRX12,HSHTPCRX12","biotype":"protein_coding","ncbi_id":"26496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7937171,"end":7941708,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]"}, {"versioned_ensembl_gene_id":"ENSG00000198221.8","gene_symbol":"AFDN-AS1","gene_name":"AFDN antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:21236]","synonyms":"MLLT4-AS1,HGC6.4,dJ431P23.3,C6orf124","biotype":"lincRNA","ncbi_id":"653483","summary":null,"start":167823876,"end":167826709,"strand":-1,"description":"AFDN antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:21236]"}, {"versioned_ensembl_gene_id":"ENSG00000225102.1","gene_symbol":"AL157373.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11990343,"end":11992012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257994.1","gene_symbol":"AC084364.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":103505411,"end":103506174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257762.5","gene_symbol":"LINC02401","gene_name":"long intergenic non-protein coding RNA 2401 [Source:HGNC Symbol;Acc:HGNC:53328]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929084","summary":null,"start":103547794,"end":103559815,"strand":1,"description":"long intergenic non-protein coding RNA 2401 [Source:HGNC Symbol;Acc:HGNC:53328]"}, {"versioned_ensembl_gene_id":"ENSG00000108239.8","gene_symbol":"TBC1D12","gene_name":"TBC1 domain family member 12 [Source:HGNC Symbol;Acc:HGNC:29082]","synonyms":"KIAA0608","biotype":"protein_coding","ncbi_id":"23232","summary":null,"start":94402504,"end":94535930,"strand":1,"description":"TBC1 domain family member 12 [Source:HGNC Symbol;Acc:HGNC:29082]"}, {"versioned_ensembl_gene_id":"ENSG00000130589.16","gene_symbol":"HELZ2","gene_name":"helicase with zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:30021]","synonyms":"PRIC285,PDIP1,KIAA1769","biotype":"protein_coding","ncbi_id":"85441","summary":"The protein encoded by this gene is a nuclear transcriptional co-activator for peroxisome proliferator activated receptor alpha. The encoded protein contains a zinc finger and is a helicase that appears to be part of the peroxisome proliferator activated receptor alpha interacting complex. This gene is a member of the DNA2/NAM7 helicase gene family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63558086,"end":63574239,"strand":-1,"description":"helicase with zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:30021]"}, {"versioned_ensembl_gene_id":"ENSG00000274315.1","gene_symbol":"AC009318.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29331434,"end":29331936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275476.1","gene_symbol":"AC009318.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29277397,"end":29277882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275278.1","gene_symbol":"AC012150.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29156448,"end":29156991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182261.3","gene_symbol":"NLRP10","gene_name":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]","synonyms":"Pynod,PAN5,NOD8,NALP10,CLR11.1","biotype":"protein_coding","ncbi_id":"338322","summary":"Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). The protein encoded by this gene belongs to the NALP protein family despite lacking the LRR region. This protein likely plays a regulatory role in the innate immune system. The protein belongs to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. Other experiments indicate that this gene acts as a multifunctional negative regulator of inflammation and apoptosis. [provided by RefSeq, Jul 2008]","start":7959424,"end":7965426,"strand":-1,"description":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]"}, {"versioned_ensembl_gene_id":"ENSG00000253261.1","gene_symbol":"AC008410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154993598,"end":154994445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087502.17","gene_symbol":"ERGIC2","gene_name":"ERGIC and golgi 2 [Source:HGNC Symbol;Acc:HGNC:30208]","synonyms":"PTX1,Erv41","biotype":"protein_coding","ncbi_id":"51290","summary":"ERGIC2, or PTX1, is a ubiquitously expressed nuclear protein that is downregulated in prostate carcinoma (Kwok et al., 2001 [PubMed 11445006]).[supplied by OMIM, Aug 2008]","start":29337352,"end":29381189,"strand":-1,"description":"ERGIC and golgi 2 [Source:HGNC Symbol;Acc:HGNC:30208]"}, {"versioned_ensembl_gene_id":"ENSG00000160570.13","gene_symbol":"DEDD2","gene_name":"death effector domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24450]","synonyms":"FLAME-3","biotype":"protein_coding","ncbi_id":"162989","summary":"This gene encodes a nuclear-localized protein containing a death effector domain (DED). The encoded protein may regulate the trafficking of caspases and other proteins into the nucleus during death receptor-induced apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":42198598,"end":42220140,"strand":-1,"description":"death effector domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24450]"}, {"versioned_ensembl_gene_id":"ENSG00000274356.1","gene_symbol":"AL355987.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":136728953,"end":136729855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114455.13","gene_symbol":"HHLA2","gene_name":"HERV-H LTR-associating 2 [Source:HGNC Symbol;Acc:HGNC:4905]","synonyms":"B7y,B7H7,B7-H5","biotype":"protein_coding","ncbi_id":"11148","summary":"This gene encodes a protein ligand found on the surface of monocytes. The encoded protein is thought to regulate cell-mediated immunity by binding to a receptor on T lymphocytes and inhibiting the proliferation of these cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":108296490,"end":108378285,"strand":1,"description":"HERV-H LTR-associating 2 [Source:HGNC Symbol;Acc:HGNC:4905]"}, {"versioned_ensembl_gene_id":"ENSG00000267742.1","gene_symbol":"FAM60CP","gene_name":"family with sequence similarity 60 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728115","summary":null,"start":60016778,"end":60017441,"strand":-1,"description":"family with sequence similarity 60 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31737]"}, {"versioned_ensembl_gene_id":"ENSG00000228330.1","gene_symbol":"AL355355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13142185,"end":13142977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267686.1","gene_symbol":"AC090771.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60125033,"end":60161195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144158.4","gene_symbol":"AL078621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113657908,"end":113658675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227989.1","gene_symbol":"AC010141.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21555852,"end":21558070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239622.1","gene_symbol":"AC005165.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25689580,"end":25689959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153086.13","gene_symbol":"ACMSD","gene_name":"aminocarboxymuconate semialdehyde decarboxylase [Source:HGNC Symbol;Acc:HGNC:19288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130013","summary":"The neuronal excitotoxin quinolinate is an intermediate in the de novo synthesis pathway of NAD from tryptophan, and has been implicated in the pathogenesis of several neurodegenerative disorders. Quinolinate is derived from alpha-amino-beta-carboxy-muconate-epsilon-semialdehyde (ACMS). ACMSD (ACMS decarboxylase; EC 4.1.1.45) can divert ACMS to a benign catabolite and thus prevent the accumulation of quinolinate from ACMS.[supplied by OMIM, Oct 2004]","start":134838547,"end":134902034,"strand":1,"description":"aminocarboxymuconate semialdehyde decarboxylase [Source:HGNC Symbol;Acc:HGNC:19288]"}, {"versioned_ensembl_gene_id":"ENSG00000226650.5","gene_symbol":"KIF4B","gene_name":"kinesin family member 4B [Source:HGNC Symbol;Acc:HGNC:6322]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285643","summary":"This gene is an intronless retrocopy of kinesin family member 4A. The protein encoded by this gene is a microtubule-based motor protein that plays vital roles in anaphase spindle dynamics and cytokinesis. [provided by RefSeq, Jul 2016]","start":155013755,"end":155018132,"strand":1,"description":"kinesin family member 4B [Source:HGNC Symbol;Acc:HGNC:6322]"}, {"versioned_ensembl_gene_id":"ENSG00000253646.1","gene_symbol":"AC010476.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155111184,"end":155112324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023734.10","gene_symbol":"STRAP","gene_name":"serine/threonine kinase receptor associated protein [Source:HGNC Symbol;Acc:HGNC:30796]","synonyms":"UNRIP,pt-wd,MAWD","biotype":"protein_coding","ncbi_id":"11171","summary":null,"start":15882391,"end":15903478,"strand":1,"description":"serine/threonine kinase receptor associated protein [Source:HGNC Symbol;Acc:HGNC:30796]"}, {"versioned_ensembl_gene_id":"ENSG00000101443.17","gene_symbol":"WFDC2","gene_name":"WAP four-disulfide core domain 2 [Source:HGNC Symbol;Acc:HGNC:15939]","synonyms":"WAP5,HE4,EDDM4,dJ461P17.6","biotype":"protein_coding","ncbi_id":"10406","summary":"This gene encodes a protein that is a member of the WFDC domain family. The WFDC domain, or WAP Signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many family members. This gene is expressed in pulmonary epithelial cells, and was also found to be expressed in some ovarian cancers. The encoded protein is a small secretory protein, which may be involved in sperm maturation. [provided by RefSeq, Jul 2008]","start":45469706,"end":45481532,"strand":1,"description":"WAP four-disulfide core domain 2 [Source:HGNC Symbol;Acc:HGNC:15939]"}, {"versioned_ensembl_gene_id":"ENSG00000169184.5","gene_symbol":"MN1","gene_name":"MN1 proto-oncogene, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:7180]","synonyms":"MGCR1-PEN,MGCR1,MGCR","biotype":"protein_coding","ncbi_id":"4330","summary":"Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008]","start":27748277,"end":27801498,"strand":-1,"description":"MN1 proto-oncogene, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:7180]"}, {"versioned_ensembl_gene_id":"ENSG00000282128.1","gene_symbol":"AC207965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70312831,"end":70374969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234391.1","gene_symbol":"AL606490.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48306769,"end":48309055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244332.1","gene_symbol":"AL138759.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":94577439,"end":94611238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279489.1","gene_symbol":"AL355377.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35001913,"end":35003663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282637.1","gene_symbol":"MAP3K14","gene_name":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]","synonyms":"FTDCR1B,NIK,HSNIK,HS","biotype":"processed_transcript","ncbi_id":"9020","summary":"This gene encodes mitogen-activated protein kinase kinase kinase 14, which is a serine/threonine protein-kinase. This kinase binds to TRAF2 and stimulates NF-kappaB activity. It shares sequence similarity with several other MAPKK kinases. It participates in an NF-kappaB-inducing signalling cascade common to receptors of the tumour-necrosis/nerve-growth factor (TNF/NGF) family and to the interleukin-1 type-I receptor. [provided by RefSeq, Jul 2008]","start":45316960,"end":45317040,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]"}, {"versioned_ensembl_gene_id":"ENSG00000273597.1","gene_symbol":"AL355377.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35001342,"end":35002994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227302.1","gene_symbol":"SSXP9","gene_name":"SSX family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30645]","synonyms":"psiSSX9","biotype":"unprocessed_pseudogene","ncbi_id":"326586","summary":null,"start":48322349,"end":48326683,"strand":1,"description":"SSX family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30645]"}, {"versioned_ensembl_gene_id":"ENSG00000119969.14","gene_symbol":"HELLS","gene_name":"helicase, lymphoid specific [Source:HGNC Symbol;Acc:HGNC:4861]","synonyms":"SMARCA6,PASG,Nbla10143,LSH","biotype":"protein_coding","ncbi_id":"3070","summary":"This gene encodes a lymphoid-specific helicase. Other helicases function in processes involving DNA strand separation, including replication, repair, recombination, and transcription. This protein is thought to be involved with cellular proliferation and may play a role in leukemogenesis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2014]","start":94501434,"end":94613905,"strand":1,"description":"helicase, lymphoid specific [Source:HGNC Symbol;Acc:HGNC:4861]"}, {"versioned_ensembl_gene_id":"ENSG00000282563.1","gene_symbol":"AC003070.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45371402,"end":45372057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223831.1","gene_symbol":"AC005006.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30598309,"end":30606687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230100.1","gene_symbol":"AL606490.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48333675,"end":48334439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229986.1","gene_symbol":"AP001042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38846247,"end":38848644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203498.2","gene_symbol":"AL139390.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6993191,"end":6995554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233496.1","gene_symbol":"SYNJ2-IT1","gene_name":"SYNJ2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41387]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874300","summary":null,"start":158001107,"end":158002383,"strand":1,"description":"SYNJ2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41387]"}, {"versioned_ensembl_gene_id":"ENSG00000235185.1","gene_symbol":"AL031727.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19591802,"end":19596832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179066.7","gene_symbol":"AC020907.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35105969,"end":35107318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227392.1","gene_symbol":"HPN-AS1","gene_name":"HPN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:47041]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128675","summary":null,"start":35059059,"end":35106304,"strand":-1,"description":"HPN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:47041]"}, {"versioned_ensembl_gene_id":"ENSG00000249695.6","gene_symbol":"AC026369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137411,"end":149169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136929.12","gene_symbol":"HEMGN","gene_name":"hemogen [Source:HGNC Symbol;Acc:HGNC:17509]","synonyms":"NDR,EDAG,CT155","biotype":"protein_coding","ncbi_id":"55363","summary":null,"start":97926791,"end":97944856,"strand":-1,"description":"hemogen [Source:HGNC Symbol;Acc:HGNC:17509]"}, {"versioned_ensembl_gene_id":"ENSG00000187922.13","gene_symbol":"LCN10","gene_name":"lipocalin 10 [Source:HGNC Symbol;Acc:HGNC:20892]","synonyms":null,"biotype":"protein_coding","ncbi_id":"414332","summary":"Members of the lipocalin family, such as LCN10, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":136738167,"end":136743356,"strand":-1,"description":"lipocalin 10 [Source:HGNC Symbol;Acc:HGNC:20892]"}, {"versioned_ensembl_gene_id":"ENSG00000229925.1","gene_symbol":"AP001043.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38888772,"end":38903905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270713.1","gene_symbol":"AL132994.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38973399,"end":38974085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227721.1","gene_symbol":"RPSAP64","gene_name":"ribosomal protein SA pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:39642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873797","summary":null,"start":38894917,"end":38895252,"strand":1,"description":"ribosomal protein SA pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:39642]"}, {"versioned_ensembl_gene_id":"ENSG00000231454.2","gene_symbol":"AL935212.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61665579,"end":61666386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256694.1","gene_symbol":"AC026369.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":164664,"end":166321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205622.9","gene_symbol":"AP001043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38863676,"end":38956467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256948.1","gene_symbol":"AC026369.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106524,"end":111850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154537.4","gene_symbol":"FAM27C","gene_name":"family with sequence similarity 27 member C [Source:HGNC Symbol;Acc:HGNC:23668]","synonyms":"FAM27A,bA7G23.5,bA374M1.5,FAM27A3,FAM27A1","biotype":"lincRNA","ncbi_id":"100132948","summary":null,"start":61854162,"end":61855331,"strand":1,"description":"family with sequence similarity 27 member C [Source:HGNC Symbol;Acc:HGNC:23668]"}, {"versioned_ensembl_gene_id":"ENSG00000261172.1","gene_symbol":"AC133919.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90110574,"end":90168225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161677.11","gene_symbol":"JOSD2","gene_name":"Josephin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28853]","synonyms":"SBBI54","biotype":"protein_coding","ncbi_id":"126119","summary":"This gene encodes a protein containing a Josephin domain. Josephin domain-containing proteins are deubiquitinating enzymes which catalyze the hydrolysis of the bond between the C-terminal glycine of the ubiquitin peptide and protein substrates. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":50505998,"end":50511353,"strand":-1,"description":"Josephin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28853]"}, {"versioned_ensembl_gene_id":"ENSG00000277624.1","gene_symbol":"AL391987.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61858710,"end":61858908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229823.1","gene_symbol":"CR847794.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31245121,"end":31245594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243304.3","gene_symbol":"AC008494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115264669,"end":115265464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179978.11","gene_symbol":"AC140134.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70094659,"end":70128434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166589.12","gene_symbol":"CDH16","gene_name":"cadherin 16 [Source:HGNC Symbol;Acc:HGNC:1755]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1014","summary":"This gene is a member of the cadherin superfamily, genes encoding calcium-dependent, membrane-associated glycoproteins. Mapped to a previously identified cluster of cadherin genes on chromosome 16q22.1, the gene localizes with superfamily members CDH1, CDH3, CDH5, CDH8 and CDH11. The protein consists of an extracellular domain containing 6 cadherin domains, a transmembrane region and a truncated cytoplasmic domain but lacks the prosequence and tripeptide HAV adhesion recognition sequence typical of most classical cadherins. Expression is exclusively in kidney, where the protein functions as the principal mediator of homotypic cellular recognition, playing a role in the morphogenic direction of tissue development. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011]","start":66908122,"end":66918984,"strand":-1,"description":"cadherin 16 [Source:HGNC Symbol;Acc:HGNC:1755]"}, {"versioned_ensembl_gene_id":"ENSG00000213529.3","gene_symbol":"AL359073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112362714,"end":112363116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254703.2","gene_symbol":"SENCR","gene_name":"smooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:44177]","synonyms":"FLI1-AS1","biotype":"antisense_RNA","ncbi_id":"100507392","summary":null,"start":128691672,"end":128696023,"strand":-1,"description":"smooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:44177]"}, {"versioned_ensembl_gene_id":"ENSG00000204805.8","gene_symbol":"FAM27E4","gene_name":"family with sequence similarity 27 member E4 [Source:HGNC Symbol;Acc:HGNC:44415]","synonyms":"FAM27E4P","biotype":"processed_pseudogene","ncbi_id":"107987001","summary":null,"start":61861995,"end":61862336,"strand":1,"description":"family with sequence similarity 27 member E4 [Source:HGNC Symbol;Acc:HGNC:44415]"}, {"versioned_ensembl_gene_id":"ENSG00000170152.4","gene_symbol":"AL391987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61861853,"end":61862567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276023.4","gene_symbol":"DUSP14","gene_name":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]","synonyms":"MKP6,MKP-L","biotype":"protein_coding","ncbi_id":"11072","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP14 contains the consensus DUSP C-terminal catalytic domain but lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":37489831,"end":37513501,"strand":1,"description":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]"}, {"versioned_ensembl_gene_id":"ENSG00000258565.1","gene_symbol":"BLZF2P","gene_name":"basic leucine zipper nuclear factor 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20049]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"317729","summary":null,"start":68867857,"end":68869951,"strand":-1,"description":"basic leucine zipper nuclear factor 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20049]"}, {"versioned_ensembl_gene_id":"ENSG00000253492.1","gene_symbol":"CDH12P3","gene_name":"cadherin 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37699]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100093624","summary":null,"start":70132679,"end":70132973,"strand":1,"description":"cadherin 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37699]"}, {"versioned_ensembl_gene_id":"ENSG00000106302.9","gene_symbol":"HYAL4","gene_name":"hyaluronoglucosaminidase 4 [Source:HGNC Symbol;Acc:HGNC:5323]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23553","summary":"This gene encodes a protein which is similar in structure to hyaluronidases but lacks hyaluronidase activity. The encoded protein acts as a chondroitin-sulfate-specific endo-beta-N-acetylgalactosaminidase; that is, it exhibits hydrolytic activity toward chondroitin sulfate chains and degrades them into oligosaccharides. Proteoglycans are formed by the covalent linkage of chondroitin sulfate chains to protein. Proteoglycans are ubiquitous components of the extracellular matrix of connective tissues and are also found at the surface of many cell types where they participate in a variety of cellular processes such as cell proliferation, differentiation, migration, cell-cell recognition, extracellular matrix deposition, and tissue morphogenesis. The expression of this gene is highest in testes and placenta. [provided by RefSeq, Apr 2019]","start":123828983,"end":123877478,"strand":1,"description":"hyaluronoglucosaminidase 4 [Source:HGNC Symbol;Acc:HGNC:5323]"}, {"versioned_ensembl_gene_id":"ENSG00000235659.1","gene_symbol":"AL391987.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61865755,"end":61866965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272600.1","gene_symbol":"AC007308.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20889206,"end":20891214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230332.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"HZFw1,LIRF","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30148763,"end":30154384,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000236896.1","gene_symbol":"AL354726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97986551,"end":97987656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254701.3","gene_symbol":"AC138866.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70197255,"end":70207745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136938.8","gene_symbol":"ANP32B","gene_name":"acidic nuclear phosphoprotein 32 family member B [Source:HGNC Symbol;Acc:HGNC:16677]","synonyms":"SSP29,PHAPI2,APRIL","biotype":"protein_coding","ncbi_id":"10541","summary":null,"start":97983361,"end":98015943,"strand":1,"description":"acidic nuclear phosphoprotein 32 family member B [Source:HGNC Symbol;Acc:HGNC:16677]"}, {"versioned_ensembl_gene_id":"ENSG00000223379.1","gene_symbol":"AL391987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61868727,"end":61887084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253816.3","gene_symbol":"AC138866.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70219918,"end":70258930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135763.9","gene_symbol":"URB2","gene_name":"URB2 ribosome biogenesis 2 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:28967]","synonyms":"KIAA0133,NPA2,NET10","biotype":"protein_coding","ncbi_id":"9816","summary":null,"start":229626234,"end":229660199,"strand":1,"description":"URB2 ribosome biogenesis 2 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:28967]"}, {"versioned_ensembl_gene_id":"ENSG00000228211.2","gene_symbol":"HYALP1","gene_name":"hyaluronoglucosaminidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5324]","synonyms":"HYAL6","biotype":"unitary_pseudogene","ncbi_id":"26062","summary":null,"start":123814139,"end":123829252,"strand":1,"description":"hyaluronoglucosaminidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5324]"}, {"versioned_ensembl_gene_id":"ENSG00000237403.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30145206,"end":30148830,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000224057.1","gene_symbol":"EGFR-AS1","gene_name":"EGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40207]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507500","summary":null,"start":55179750,"end":55188934,"strand":-1,"description":"EGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40207]"}, {"versioned_ensembl_gene_id":"ENSG00000242060.1","gene_symbol":"RPS3AP49","gene_name":"ribosomal protein S3a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400652","summary":null,"start":60149576,"end":60150365,"strand":1,"description":"ribosomal protein S3a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36810]"}, {"versioned_ensembl_gene_id":"ENSG00000204003.8","gene_symbol":"AL355987.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136738167,"end":136748453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175509.8","gene_symbol":"AL078621.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113667478,"end":113668621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233479.1","gene_symbol":"AC017074.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113669166,"end":113673191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138231.12","gene_symbol":"DBR1","gene_name":"debranching RNA lariats 1 [Source:HGNC Symbol;Acc:HGNC:15594]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51163","summary":"The protein encoded by this gene is an RNA lariat debranching enzyme that hydrolyzes 2'-5' prime branched phosphodiester bonds. The encoded protein specifically targets the bonds at the branch point of excised lariat intron RNA, converting them to linear molecules that are then degraded. This protein may also be involved in retroviral replication. [provided by RefSeq, Nov 2011]","start":138161012,"end":138174949,"strand":-1,"description":"debranching RNA lariats 1 [Source:HGNC Symbol;Acc:HGNC:15594]"}, {"versioned_ensembl_gene_id":"ENSG00000173250.2","gene_symbol":"GPR151","gene_name":"G protein-coupled receptor 151 [Source:HGNC Symbol;Acc:HGNC:23624]","synonyms":"PGR7,GALR4","biotype":"protein_coding","ncbi_id":"134391","summary":"This gene encodes an orphan member of the class A rhodopsin-like family of G-protein-coupled receptors (GPCRs). Within the rhodopsin-like family, this gene is a member of the SOG subfamily that includes somatostatin, opioid, galanin, and kisspeptin receptors. The orthologous mouse gene has a restricted pattern of neuronal expression which is induced following nerve injury. All GPCRs have a transmembrane domain that includes seven transmembrane alpha-helices. A general feature of GPCR signaling is the agonist-induced conformational change in the receptor, leading to activation of the heterotrimeric G protein. The activated G protein then binds to and activates numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017]","start":146513103,"end":146516190,"strand":-1,"description":"G protein-coupled receptor 151 [Source:HGNC Symbol;Acc:HGNC:23624]"}, {"versioned_ensembl_gene_id":"ENSG00000236930.1","gene_symbol":"AC099782.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45883640,"end":45884113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173585.15","gene_symbol":"CCR9","gene_name":"C-C motif chemokine receptor 9 [Source:HGNC Symbol;Acc:HGNC:1610]","synonyms":"GPR28,GPR-9-6,CDw199","biotype":"protein_coding","ncbi_id":"10803","summary":"The protein encoded by this gene is a G protein-coupled receptor with seven transmembrane domains that belongs to the beta chemokine receptor family. Chemokines and their receptors are key regulators of thymocyte migration and maturation in normal and inflammation conditions. This gene is differentially expressed in T lymphocytes of the small intestine and colon, and its interaction with chemokine 25 contributes to intestinal intra-epithelial lymphocyte homing to the small intestine. This suggests a role for this gene in directing immune responses to different segments of the gastrointestinal tract. This gene and its exclusive ligand, chemokine 25, are overexpressed in a variety of malignant tumors and are closely associated with tumor proliferation, apoptosis, invasion, migration and drug resistance. This gene maps to the chemokine receptor gene cluster. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2020]","start":45886504,"end":45903177,"strand":1,"description":"C-C motif chemokine receptor 9 [Source:HGNC Symbol;Acc:HGNC:1610]"}, {"versioned_ensembl_gene_id":"ENSG00000232722.3","gene_symbol":"MROH4P","gene_name":"maestro heat like repeat family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44902]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"101154686","summary":null,"start":142567260,"end":142577881,"strand":-1,"description":"maestro heat like repeat family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44902]"}, {"versioned_ensembl_gene_id":"ENSG00000267206.5","gene_symbol":"LCN6","gene_name":"lipocalin 6 [Source:HGNC Symbol;Acc:HGNC:17337]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158062","summary":null,"start":136744011,"end":136748528,"strand":-1,"description":"lipocalin 6 [Source:HGNC Symbol;Acc:HGNC:17337]"}, {"versioned_ensembl_gene_id":"ENSG00000228100.1","gene_symbol":"LINC01820","gene_name":"long intergenic non-protein coding RNA 1820 [Source:HGNC Symbol;Acc:HGNC:52625]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374582","summary":null,"start":46392297,"end":46394167,"strand":-1,"description":"long intergenic non-protein coding RNA 1820 [Source:HGNC Symbol;Acc:HGNC:52625]"}, {"versioned_ensembl_gene_id":"ENSG00000197785.13","gene_symbol":"ATAD3A","gene_name":"ATPase family, AAA domain containing 3A [Source:HGNC Symbol;Acc:HGNC:25567]","synonyms":"FLJ10709","biotype":"protein_coding","ncbi_id":"55210","summary":"This gene encodes a ubiquitously expressed mitochondrial membrane protein that contributes to mitochondrial dynamics, nucleoid organization, protein translation, cell growth, and cholesterol metabolism. This gene is a member of the ATPase family AAA-domain containing 3 gene family which, in humans, includes two other paralogs. Naturally occurring mutations in this gene are associated with distinct neurological syndromes including Harel-Yoon syndrome. High-level expression of this gene is associated with poor survival in breast cancer patients. A homozygous knockout of the orthologous gene in mice results in embryonic lethality at day 7.5 due to growth retardation and defective development of the trophoblast lineage. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":1512151,"end":1534687,"strand":1,"description":"ATPase family, AAA domain containing 3A [Source:HGNC Symbol;Acc:HGNC:25567]"}, {"versioned_ensembl_gene_id":"ENSG00000107872.12","gene_symbol":"FBXL15","gene_name":"F-box and leucine rich repeat protein 15 [Source:HGNC Symbol;Acc:HGNC:28155]","synonyms":"MGC11279,FBXO37,Fbl15","biotype":"protein_coding","ncbi_id":"79176","summary":null,"start":102419189,"end":102423136,"strand":1,"description":"F-box and leucine rich repeat protein 15 [Source:HGNC Symbol;Acc:HGNC:28155]"}, {"versioned_ensembl_gene_id":"ENSG00000177575.12","gene_symbol":"CD163","gene_name":"CD163 molecule [Source:HGNC Symbol;Acc:HGNC:1631]","synonyms":"SCARI1,MM130,M130","biotype":"protein_coding","ncbi_id":"9332","summary":"The protein encoded by this gene is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. It functions as an acute phase-regulated receptor involved in the clearance and endocytosis of hemoglobin/haptoglobin complexes by macrophages, and may thereby protect tissues from free hemoglobin-mediated oxidative damage. This protein may also function as an innate immune sensor for bacteria and inducer of local inflammation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":7470813,"end":7503893,"strand":-1,"description":"CD163 molecule [Source:HGNC Symbol;Acc:HGNC:1631]"}, {"versioned_ensembl_gene_id":"ENSG00000266826.2","gene_symbol":"AC011195.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":58660424,"end":58692018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243188.1","gene_symbol":"HNRNPA1P17","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39135]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421376","summary":null,"start":108325520,"end":108326814,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39135]"}, {"versioned_ensembl_gene_id":"ENSG00000227523.1","gene_symbol":"RPS20P15","gene_name":"ribosomal protein S20 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271085","summary":null,"start":27462506,"end":27462816,"strand":1,"description":"ribosomal protein S20 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36340]"}, {"versioned_ensembl_gene_id":"ENSG00000198326.9","gene_symbol":"TMEM239","gene_name":"transmembrane protein 239 [Source:HGNC Symbol;Acc:HGNC:40044]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288797","summary":null,"start":2816302,"end":2820284,"strand":1,"description":"transmembrane protein 239 [Source:HGNC Symbol;Acc:HGNC:40044]"}, {"versioned_ensembl_gene_id":"ENSG00000203414.2","gene_symbol":"BTBD7P1","gene_name":"BTB domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44875]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441548","summary":null,"start":13156684,"end":13158136,"strand":-1,"description":"BTB domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44875]"}, {"versioned_ensembl_gene_id":"ENSG00000181924.6","gene_symbol":"COA4","gene_name":"cytochrome c oxidase assembly factor 4 homolog [Source:HGNC Symbol;Acc:HGNC:24604]","synonyms":"E2IG2,CMC3,CHCHD8","biotype":"protein_coding","ncbi_id":"51287","summary":null,"start":73872667,"end":73876988,"strand":-1,"description":"cytochrome c oxidase assembly factor 4 homolog [Source:HGNC Symbol;Acc:HGNC:24604]"}, {"versioned_ensembl_gene_id":"ENSG00000263517.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30211301,"end":30211463,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000170881.4","gene_symbol":"RNF139","gene_name":"ring finger protein 139 [Source:HGNC Symbol;Acc:HGNC:17023]","synonyms":"TRC8,RCA1,HRCA1","biotype":"protein_coding","ncbi_id":"11236","summary":"The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008]","start":124474738,"end":124487914,"strand":1,"description":"ring finger protein 139 [Source:HGNC Symbol;Acc:HGNC:17023]"}, {"versioned_ensembl_gene_id":"ENSG00000237540.1","gene_symbol":"RPL36AP36","gene_name":"ribosomal protein L36a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644834","summary":null,"start":13159477,"end":13159777,"strand":-1,"description":"ribosomal protein L36a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36326]"}, {"versioned_ensembl_gene_id":"ENSG00000155313.15","gene_symbol":"USP25","gene_name":"ubiquitin specific peptidase 25 [Source:HGNC Symbol;Acc:HGNC:12624]","synonyms":"USP21","biotype":"protein_coding","ncbi_id":"29761","summary":"Ubiquitin (MIM 191339) is a highly conserved 76-amino acid protein involved in regulation of intracellular protein breakdown, cell cycle regulation, and stress response. Ubiquitin is released from degraded proteins by disassembly of the polyubiquitin chains, which is mediated by ubiquitin-specific proteases (USPs), such as USP25 (Valero et al., 1999 [PubMed 10644437]).[supplied by OMIM, Mar 2008]","start":15730025,"end":15880069,"strand":1,"description":"ubiquitin specific peptidase 25 [Source:HGNC Symbol;Acc:HGNC:12624]"}, {"versioned_ensembl_gene_id":"ENSG00000121101.15","gene_symbol":"TEX14","gene_name":"testis expressed 14, intercellular bridge forming factor [Source:HGNC Symbol;Acc:HGNC:11737]","synonyms":"CT113","biotype":"protein_coding","ncbi_id":"56155","summary":"The protein encoded by this gene is necessary for intercellular bridges in germ cells, which are required for spermatogenesis. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]","start":58556678,"end":58692055,"strand":-1,"description":"testis expressed 14, intercellular bridge forming factor [Source:HGNC Symbol;Acc:HGNC:11737]"}, {"versioned_ensembl_gene_id":"ENSG00000173480.10","gene_symbol":"ZNF417","gene_name":"zinc finger protein 417 [Source:HGNC Symbol;Acc:HGNC:20646]","synonyms":"MGC34079","biotype":"protein_coding","ncbi_id":"147687","summary":null,"start":57900296,"end":57916610,"strand":-1,"description":"zinc finger protein 417 [Source:HGNC Symbol;Acc:HGNC:20646]"}, {"versioned_ensembl_gene_id":"ENSG00000258713.2","gene_symbol":"C20orf141","gene_name":"chromosome 20 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:16134]","synonyms":"dJ860F19.4","biotype":"protein_coding","ncbi_id":"128653","summary":null,"start":2814987,"end":2815833,"strand":1,"description":"chromosome 20 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:16134]"}, {"versioned_ensembl_gene_id":"ENSG00000273609.1","gene_symbol":"AC005562.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30617680,"end":30617790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223756.6","gene_symbol":"TSSC2","gene_name":"tumor suppressing subtransferable candidate 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:12384]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"650368","summary":null,"start":3380961,"end":3408978,"strand":1,"description":"tumor suppressing subtransferable candidate 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:12384]"}, {"versioned_ensembl_gene_id":"ENSG00000154545.16","gene_symbol":"MAGED4","gene_name":"MAGE family member D4 [Source:HGNC Symbol;Acc:HGNC:23793]","synonyms":"MGC3210,MAGE1,MAGE-E1,KIAA1859","biotype":"protein_coding","ncbi_id":"728239","summary":null,"start":52184823,"end":52192268,"strand":1,"description":"MAGE family member D4 [Source:HGNC Symbol;Acc:HGNC:23793]"}, {"versioned_ensembl_gene_id":"ENSG00000214719.11","gene_symbol":"AC005562.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30576464,"end":30672789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059915.16","gene_symbol":"PSD","gene_name":"pleckstrin and Sec7 domain containing [Source:HGNC Symbol;Acc:HGNC:9507]","synonyms":"EFA6A,EFA6,TYL,PSD1,KIAA2011","biotype":"protein_coding","ncbi_id":"5662","summary":"This gene encodes a Plekstrin homology and SEC7 domains-containing protein that functions as a guanine nucleotide exchange factor. The encoded protein regulates signal transduction by activating ADP-ribosylation factor 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":102402617,"end":102421539,"strand":-1,"description":"pleckstrin and Sec7 domain containing [Source:HGNC Symbol;Acc:HGNC:9507]"}, {"versioned_ensembl_gene_id":"ENSG00000273680.1","gene_symbol":"AC009318.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29332733,"end":29333383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033867.16","gene_symbol":"SLC4A7","gene_name":"solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]","synonyms":"SLC4A6,SBC2,NBC3","biotype":"protein_coding","ncbi_id":"9497","summary":"This locus encodes a sodium bicarbonate cotransporter. The encoded transmembrane protein appears to transport sodium and bicarbonate ions in a 1:1 ratio, and is thus considered an electroneutral cotransporter. The encoded protein likely plays a critical role in regulation of intracellular pH involved in visual and auditory sensory transmission. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]","start":27372721,"end":27484420,"strand":-1,"description":"solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]"}, {"versioned_ensembl_gene_id":"ENSG00000237211.2","gene_symbol":"SETP4","gene_name":"SET pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642869","summary":null,"start":84755136,"end":84756003,"strand":1,"description":"SET pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42923]"}, {"versioned_ensembl_gene_id":"ENSG00000131697.17","gene_symbol":"NPHP4","gene_name":"nephrocystin 4 [Source:HGNC Symbol;Acc:HGNC:19104]","synonyms":"SLSN4,POC10,KIAA0673","biotype":"protein_coding","ncbi_id":"261734","summary":"This gene encodes a protein involved in renal tubular development and function. This protein interacts with nephrocystin, and belongs to a multifunctional complex that is localized to actin- and microtubule-based structures. Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior-Loken syndrome type 4, a combination of nephronophthisis and retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":5862811,"end":5992473,"strand":-1,"description":"nephrocystin 4 [Source:HGNC Symbol;Acc:HGNC:19104]"}, {"versioned_ensembl_gene_id":"ENSG00000229896.2","gene_symbol":"AL157373.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12007670,"end":12008856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124831.18","gene_symbol":"LRRFIP1","gene_name":"LRR binding FLII interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6702]","synonyms":"TRIP,HUFI-1,GCF-2,FLIIAP1,FLAP-1","biotype":"protein_coding","ncbi_id":"9208","summary":null,"start":237627576,"end":237813682,"strand":1,"description":"LRR binding FLII interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6702]"}, {"versioned_ensembl_gene_id":"ENSG00000241690.3","gene_symbol":"AL035460.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2814968,"end":2818066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270435.1","gene_symbol":"AC068733.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6297189,"end":6298606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198466.11","gene_symbol":"ZNF587","gene_name":"zinc finger protein 587 [Source:HGNC Symbol;Acc:HGNC:30955]","synonyms":"FLJ14710,ZF6,UBF-fl,FLJ20813","biotype":"protein_coding","ncbi_id":"84914","summary":null,"start":57849857,"end":57865112,"strand":1,"description":"zinc finger protein 587 [Source:HGNC Symbol;Acc:HGNC:30955]"}, {"versioned_ensembl_gene_id":"ENSG00000095951.16","gene_symbol":"HIVEP1","gene_name":"human immunodeficiency virus type I enhancer binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4920]","synonyms":"CIRIP,ZNF40A,ZNF40,ZAS1,Schnurri-1,PRDII-BF1,MBP-1,CRYBP1","biotype":"protein_coding","ncbi_id":"3096","summary":"This gene encodes a transcription factor belonging to the ZAS family, members of which are large proteins that contain a ZAS domain - a modular protein structure consisting of a pair of C2H2 zinc fingers with an acidic-rich region and a serine/threonine-rich sequence. These proteins bind specifically to the DNA sequence motif, GGGACTTTCC, found in the enhancer elements of several viral promoters, including human immunodeficiency virus (HIV), and to related sequences found in the enhancer elements of a number of cellular promoters. This protein binds to this sequence motif, suggesting a role in the transcriptional regulation of both viral and cellular genes. [provided by RefSeq, Oct 2011]","start":12008762,"end":12164999,"strand":1,"description":"human immunodeficiency virus type I enhancer binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4920]"}, {"versioned_ensembl_gene_id":"ENSG00000198576.3","gene_symbol":"ARC","gene_name":"activity regulated cytoskeleton associated protein [Source:HGNC Symbol;Acc:HGNC:648]","synonyms":"KIAA0278,Arg3.1","biotype":"protein_coding","ncbi_id":"23237","summary":null,"start":142611044,"end":142614472,"strand":-1,"description":"activity regulated cytoskeleton associated protein [Source:HGNC Symbol;Acc:HGNC:648]"}, {"versioned_ensembl_gene_id":"ENSG00000167470.12","gene_symbol":"MIDN","gene_name":"midnolin [Source:HGNC Symbol;Acc:HGNC:16298]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90007","summary":null,"start":1248553,"end":1259140,"strand":1,"description":"midnolin [Source:HGNC Symbol;Acc:HGNC:16298]"}, {"versioned_ensembl_gene_id":"ENSG00000183607.9","gene_symbol":"GKN2","gene_name":"gastrokine 2 [Source:HGNC Symbol;Acc:HGNC:24588]","synonyms":"GDDR,BRICD1B,blottin,VLTI465,TFIZ1,PRO813","biotype":"protein_coding","ncbi_id":"200504","summary":"The secretory protein encoded by this gene is produced in gastric surface mucous cells, where it can bind trefoil factor family peptide 1 or gastrokine-1. This gene may be a tumor suppressor gene, as its expression is markedly decreased in gastric cancer tissues. The encoded protein interacts with gastrokine-1 and regulates homeostasis of the gastric mucosa. [provided by RefSeq, Dec 2015]","start":68945232,"end":68952970,"strand":-1,"description":"gastrokine 2 [Source:HGNC Symbol;Acc:HGNC:24588]"}, {"versioned_ensembl_gene_id":"ENSG00000227709.4","gene_symbol":"AC091607.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156175852,"end":156176911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227359.1","gene_symbol":"AC017074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113677702,"end":113704078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248568.1","gene_symbol":"KRT8P48","gene_name":"keratin 8 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100887067","summary":null,"start":146706381,"end":146707600,"strand":-1,"description":"keratin 8 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48344]"}, {"versioned_ensembl_gene_id":"ENSG00000181588.16","gene_symbol":"MEX3D","gene_name":"mex-3 RNA binding family member D [Source:HGNC Symbol;Acc:HGNC:16734]","synonyms":"OK/SW-cl.4,KIAA2031,Tino,RNF193,RKHD1","biotype":"protein_coding","ncbi_id":"399664","summary":null,"start":1554669,"end":1568058,"strand":-1,"description":"mex-3 RNA binding family member D [Source:HGNC Symbol;Acc:HGNC:16734]"}, {"versioned_ensembl_gene_id":"ENSG00000242370.1","gene_symbol":"KCNAB1-AS1","gene_name":"KCNAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40316]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874084","summary":null,"start":156441157,"end":156446905,"strand":-1,"description":"KCNAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40316]"}, {"versioned_ensembl_gene_id":"ENSG00000264943.1","gene_symbol":"SH3GL1P2","gene_name":"SH3 domain containing GRB2 like 1, endophilin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10836]","synonyms":"SH3GLP2,CNSA-P2","biotype":"processed_pseudogene","ncbi_id":"6459","summary":null,"start":30624413,"end":30625494,"strand":1,"description":"SH3 domain containing GRB2 like 1, endophilin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10836]"}, {"versioned_ensembl_gene_id":"ENSG00000250407.1","gene_symbol":"AC008728.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146563226,"end":146617004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178660.6","gene_symbol":"ARMC10P1","gene_name":"armadillo repeat containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389137","summary":null,"start":94506766,"end":94507620,"strand":-1,"description":"armadillo repeat containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43646]"}, {"versioned_ensembl_gene_id":"ENSG00000189398.5","gene_symbol":"OR7E12P","gene_name":"olfactory receptor family 7 subfamily E member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:8383]","synonyms":"OR7E79P,OR7E58P,OR11-3","biotype":"unprocessed_pseudogene","ncbi_id":"10821","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3390780,"end":3391752,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:8383]"}, {"versioned_ensembl_gene_id":"ENSG00000248121.8","gene_symbol":"SMURF2P1","gene_name":"SMAD specific E3 ubiquitin protein ligase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44402]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107133516","summary":null,"start":30600796,"end":30615980,"strand":1,"description":"SMAD specific E3 ubiquitin protein ligase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44402]"}, {"versioned_ensembl_gene_id":"ENSG00000271477.1","gene_symbol":"AC010591.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155397291,"end":155398353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242911.1","gene_symbol":"AC140059.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94935760,"end":94936120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169282.17","gene_symbol":"KCNAB1","gene_name":"potassium voltage-gated channel subfamily A member regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6228]","synonyms":"KCNA1B,hKvBeta3,hKvb3,AKR6A3,Kvb1.3","biotype":"protein_coding","ncbi_id":"7881","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member includes distinct isoforms which are encoded by alternatively spliced transcript variants of this gene. Some of these isoforms are beta subunits, which form heteromultimeric complexes with alpha subunits and modulate the activity of the pore-forming alpha subunits. [provided by RefSeq, Apr 2015]","start":156037701,"end":156539138,"strand":1,"description":"potassium voltage-gated channel subfamily A member regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6228]"}, {"versioned_ensembl_gene_id":"ENSG00000270442.1","gene_symbol":"AC008725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155491336,"end":155493598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234629.1","gene_symbol":"WDR82P1","gene_name":"WD repeat domain 82 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32447]","synonyms":"WDR82B,WDR82,SW2,hCG26824","biotype":"processed_pseudogene","ncbi_id":"728505","summary":null,"start":94937086,"end":94938024,"strand":-1,"description":"WD repeat domain 82 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32447]"}, {"versioned_ensembl_gene_id":"ENSG00000156475.18","gene_symbol":"PPP2R2B","gene_name":"protein phosphatase 2 regulatory subunit Bbeta [Source:HGNC Symbol;Acc:HGNC:9305]","synonyms":"SCA12,PR55-BETA,PR52B,B55beta","biotype":"protein_coding","ncbi_id":"5521","summary":"The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a beta isoform of the regulatory subunit B55 subfamily. Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12), a disease caused by degeneration of the cerebellum, sometimes involving the brainstem and spinal cord, and in resulting in poor coordination of speech and body movements. Multiple alternatively spliced variants, which encode different isoforms, have been identified for this gene. The 5' UTR of some of these variants includes a CAG trinucleotide repeat sequence (7-28 copies) that can be expanded to 55-78 copies in cases of SCA12. [provided by RefSeq, Jul 2016]","start":146581146,"end":147084784,"strand":-1,"description":"protein phosphatase 2 regulatory subunit Bbeta [Source:HGNC Symbol;Acc:HGNC:9305]"}, {"versioned_ensembl_gene_id":"ENSG00000231268.9","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32247977,"end":32251333,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000231421.7","gene_symbol":"AC011840.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30573471,"end":30577000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246695.7","gene_symbol":"RASSF8-AS1","gene_name":"RASSF8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48637]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506451","summary":null,"start":25939329,"end":25959765,"strand":-1,"description":"RASSF8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48637]"}, {"versioned_ensembl_gene_id":"ENSG00000199282.1","gene_symbol":"SNORA9","gene_name":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]","synonyms":"ACA9,SNORA9A","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":72586680,"end":72586810,"strand":1,"description":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]"}, {"versioned_ensembl_gene_id":"ENSG00000269304.1","gene_symbol":"FKBP1AP1","gene_name":"FK506 binding protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3714]","synonyms":"FKBP1P1","biotype":"processed_pseudogene","ncbi_id":"2282","summary":null,"start":57826461,"end":57826778,"strand":-1,"description":"FK506 binding protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3714]"}, {"versioned_ensembl_gene_id":"ENSG00000138433.15","gene_symbol":"CIR1","gene_name":"corepressor interacting with RBPJ, 1 [Source:HGNC Symbol;Acc:HGNC:24217]","synonyms":"CIR","biotype":"protein_coding","ncbi_id":"9541","summary":null,"start":174348022,"end":174395715,"strand":-1,"description":"corepressor interacting with RBPJ, 1 [Source:HGNC Symbol;Acc:HGNC:24217]"}, {"versioned_ensembl_gene_id":"ENSG00000268750.6","gene_symbol":"AC010522.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57819719,"end":57858941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250462.8","gene_symbol":"LRRC37BP1","gene_name":"leucine rich repeat containing 37B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25390]","synonyms":"LRRC37B2,DKFZp667M2411","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"147172","summary":null,"start":30629680,"end":30637466,"strand":1,"description":"leucine rich repeat containing 37B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25390]"}, {"versioned_ensembl_gene_id":"ENSG00000255449.1","gene_symbol":"AP002812.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77866412,"end":77870091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265794.5","gene_symbol":"AC005899.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32324431,"end":32360700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149262.16","gene_symbol":"INTS4","gene_name":"integrator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:25048]","synonyms":"MST093,MGC16733,INT4","biotype":"protein_coding","ncbi_id":"92105","summary":"INTS4 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":77878720,"end":77994678,"strand":-1,"description":"integrator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:25048]"}, {"versioned_ensembl_gene_id":"ENSG00000226529.1","gene_symbol":"MTND1P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38728]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499468","summary":null,"start":8371663,"end":8372030,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38728]"}, {"versioned_ensembl_gene_id":"ENSG00000083828.15","gene_symbol":"ZNF586","gene_name":"zinc finger protein 586 [Source:HGNC Symbol;Acc:HGNC:25949]","synonyms":"FLJ20070","biotype":"protein_coding","ncbi_id":"54807","summary":null,"start":57769655,"end":57819939,"strand":1,"description":"zinc finger protein 586 [Source:HGNC Symbol;Acc:HGNC:25949]"}, {"versioned_ensembl_gene_id":"ENSG00000161016.17","gene_symbol":"RPL8","gene_name":"ribosomal protein L8 [Source:HGNC Symbol;Acc:HGNC:10368]","synonyms":"L8","biotype":"protein_coding","ncbi_id":"6132","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L2P family of ribosomal proteins. It is located in the cytoplasm. In rat, the protein associates with the 5.8S rRNA, very likely participates in the binding of aminoacyl-tRNA, and is a constituent of the elongation factor 2-binding site at the ribosomal subunit interface. Alternatively spliced transcript variants encoding the same protein exist. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":144789765,"end":144792587,"strand":-1,"description":"ribosomal protein L8 [Source:HGNC Symbol;Acc:HGNC:10368]"}, {"versioned_ensembl_gene_id":"ENSG00000175575.12","gene_symbol":"PAAF1","gene_name":"proteasomal ATPase associated factor 1 [Source:HGNC Symbol;Acc:HGNC:25687]","synonyms":"WDR71,Rpn14,FLJ11848","biotype":"protein_coding","ncbi_id":"80227","summary":"This gene encodes a WD repeat-containing protein involved in regulation of association of proteasome components. During HIV infection, the encoded protein is thought to promote provirus transcription through recruitment of the 19S regulatory complex. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012]","start":73876699,"end":73931124,"strand":1,"description":"proteasomal ATPase associated factor 1 [Source:HGNC Symbol;Acc:HGNC:25687]"}, {"versioned_ensembl_gene_id":"ENSG00000282715.1","gene_symbol":"ANKRD20A9P","gene_name":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"284232","summary":null,"start":18816718,"end":18880683,"strand":-1,"description":"ankyrin repeat domain 20 family member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42023]"}, {"versioned_ensembl_gene_id":"ENSG00000265139.1","gene_symbol":"AC005899.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32328441,"end":32329395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125247.15","gene_symbol":"TMTC4","gene_name":"transmembrane and tetratricopeptide repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25904]","synonyms":"FLJ22153,FLJ14624","biotype":"protein_coding","ncbi_id":"84899","summary":"This gene encodes a transmembrane protein that belongs to family of proteins containing an N-terminal transmembrane domain and a C-terminal tetratricopeptide repeat (TPR) domain. TPR domains mediate protein-protein interactions in various cellular processes, such as synaptic vesicle fusion, protein folding, and protein translocation. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, Apr 2017]","start":100603927,"end":100675093,"strand":-1,"description":"transmembrane and tetratricopeptide repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25904]"}, {"versioned_ensembl_gene_id":"ENSG00000281804.1","gene_symbol":"AC068446.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21250180,"end":21260147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166492.9","gene_symbol":"FAM86GP","gene_name":"family with sequence similarity 86 member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42358]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387745","summary":null,"start":3410352,"end":3422496,"strand":-1,"description":"family with sequence similarity 86 member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42358]"}, {"versioned_ensembl_gene_id":"ENSG00000229547.4","gene_symbol":"UBE2DNL","gene_name":"ubiquitin conjugating enzyme E2 D N-terminal like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28656]","synonyms":"MGC42638","biotype":"transcribed_processed_pseudogene","ncbi_id":"100131816","summary":null,"start":84934151,"end":84934890,"strand":1,"description":"ubiquitin conjugating enzyme E2 D N-terminal like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28656]"}, {"versioned_ensembl_gene_id":"ENSG00000143494.15","gene_symbol":"VASH2","gene_name":"vasohibin 2 [Source:HGNC Symbol;Acc:HGNC:25723]","synonyms":"FLJ12505","biotype":"protein_coding","ncbi_id":"79805","summary":null,"start":212950520,"end":212992037,"strand":1,"description":"vasohibin 2 [Source:HGNC Symbol;Acc:HGNC:25723]"}, {"versioned_ensembl_gene_id":"ENSG00000131042.14","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"LIR-2,MIR10,ILT4,MIR-10,CD85d,LIR2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54273821,"end":54281184,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000143512.12","gene_symbol":"HHIPL2","gene_name":"HHIP like 2 [Source:HGNC Symbol;Acc:HGNC:25842]","synonyms":"KIAA1822L,FLJ13840","biotype":"protein_coding","ncbi_id":"79802","summary":null,"start":222522258,"end":222548103,"strand":-1,"description":"HHIP like 2 [Source:HGNC Symbol;Acc:HGNC:25842]"}, {"versioned_ensembl_gene_id":"ENSG00000229697.2","gene_symbol":"AL391987.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61898805,"end":61911022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237852.1","gene_symbol":"AC119800.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65486406,"end":65494188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269867.1","gene_symbol":"AC010326.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":57867038,"end":57868172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237226.1","gene_symbol":"AC127526.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3549745,"end":3550519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270804.1","gene_symbol":"AC010326.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":57867885,"end":57868834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234743.1","gene_symbol":"EIF5AP4","gene_name":"eukaryotic translation initiation factor 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31442]","synonyms":"EIF5AL3","biotype":"processed_pseudogene","ncbi_id":"642592","summary":null,"start":80247219,"end":80247683,"strand":-1,"description":"eukaryotic translation initiation factor 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31442]"}, {"versioned_ensembl_gene_id":"ENSG00000123094.15","gene_symbol":"RASSF8","gene_name":"Ras association domain family member 8 [Source:HGNC Symbol;Acc:HGNC:13232]","synonyms":"HoJ-1,C12orf2","biotype":"protein_coding","ncbi_id":"11228","summary":"This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":25959029,"end":26079892,"strand":1,"description":"Ras association domain family member 8 [Source:HGNC Symbol;Acc:HGNC:13232]"}, {"versioned_ensembl_gene_id":"ENSG00000284639.1","gene_symbol":"AP006294.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3580927,"end":3581135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234850.1","gene_symbol":"MTND2P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499457","summary":null,"start":8372241,"end":8372710,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38727]"}, {"versioned_ensembl_gene_id":"ENSG00000284605.1","gene_symbol":"AC127526.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3429758,"end":3500621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078401.6","gene_symbol":"EDN1","gene_name":"endothelin 1 [Source:HGNC Symbol;Acc:HGNC:3176]","synonyms":"ET1","biotype":"protein_coding","ncbi_id":"1906","summary":"This gene encodes a preproprotein that is proteolytically processed to generate a secreted peptide that belongs to the endothelin/sarafotoxin family. This peptide is a potent vasoconstrictor and its cognate receptors are therapeutic targets in the treatment of pulmonary arterial hypertension. Aberrant expression of this gene may promote tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":12290363,"end":12297194,"strand":1,"description":"endothelin 1 [Source:HGNC Symbol;Acc:HGNC:3176]"}, {"versioned_ensembl_gene_id":"ENSG00000178935.5","gene_symbol":"ZNF552","gene_name":"zinc finger protein 552 [Source:HGNC Symbol;Acc:HGNC:26135]","synonyms":"FLJ21603","biotype":"protein_coding","ncbi_id":"79818","summary":null,"start":57803841,"end":57814913,"strand":-1,"description":"zinc finger protein 552 [Source:HGNC Symbol;Acc:HGNC:26135]"}, {"versioned_ensembl_gene_id":"ENSG00000223688.2","gene_symbol":"AC127526.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3559657,"end":3560022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255367.3","gene_symbol":"AC127526.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":3481520,"end":3581211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224570.1","gene_symbol":"AC097063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65576129,"end":65578380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213118.4","gene_symbol":"CHCHD2P4","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874507","summary":null,"start":134393142,"end":134393900,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39588]"}, {"versioned_ensembl_gene_id":"ENSG00000222300.1","gene_symbol":"RNU2-21P","gene_name":"RNA, U2 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:48514]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480206","summary":null,"start":158935798,"end":158935985,"strand":-1,"description":"RNA, U2 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:48514]"}, {"versioned_ensembl_gene_id":"ENSG00000207569.2","gene_symbol":"MIR433","gene_name":"microRNA 433 [Source:HGNC Symbol;Acc:HGNC:32026]","synonyms":"MIRN433,hsa-mir-433","biotype":"miRNA","ncbi_id":"574034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100881886,"end":100881978,"strand":1,"description":"microRNA 433 [Source:HGNC Symbol;Acc:HGNC:32026]"}, {"versioned_ensembl_gene_id":"ENSG00000264966.1","gene_symbol":"MIR5094","gene_name":"microRNA 5094 [Source:HGNC Symbol;Acc:HGNC:43519]","synonyms":"hsa-mir-5094","biotype":"miRNA","ncbi_id":"100847059","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89850637,"end":89850721,"strand":-1,"description":"microRNA 5094 [Source:HGNC Symbol;Acc:HGNC:43519]"}, {"versioned_ensembl_gene_id":"ENSG00000274941.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000224614.1","gene_symbol":"TNK2-AS1","gene_name":"TNK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49093]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128262","summary":null,"start":195908076,"end":195911257,"strand":1,"description":"TNK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49093]"}, {"versioned_ensembl_gene_id":"ENSG00000206150.3","gene_symbol":"RNASE13","gene_name":"ribonuclease A family member 13 (inactive) [Source:HGNC Symbol;Acc:HGNC:25285]","synonyms":"RAL1","biotype":"protein_coding","ncbi_id":"440163","summary":null,"start":21032820,"end":21034785,"strand":-1,"description":"ribonuclease A family member 13 (inactive) [Source:HGNC Symbol;Acc:HGNC:25285]"}, {"versioned_ensembl_gene_id":"ENSG00000173621.8","gene_symbol":"LRFN4","gene_name":"leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28456]","synonyms":"SALM3.,MGC3103,FIGLER6","biotype":"protein_coding","ncbi_id":"78999","summary":null,"start":66856647,"end":66860475,"strand":1,"description":"leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28456]"}, {"versioned_ensembl_gene_id":"ENSG00000266736.1","gene_symbol":"GTF2IP6","gene_name":"general transcription factor IIi pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51718]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927390","summary":null,"start":27019527,"end":27047934,"strand":-1,"description":"general transcription factor IIi pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51718]"}, {"versioned_ensembl_gene_id":"ENSG00000141854.9","gene_symbol":"MISP3","gene_name":"MISP family member 3 [Source:HGNC Symbol;Acc:HGNC:26963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113230","summary":null,"start":14072536,"end":14075062,"strand":1,"description":"MISP family member 3 [Source:HGNC Symbol;Acc:HGNC:26963]"}, {"versioned_ensembl_gene_id":"ENSG00000169683.7","gene_symbol":"LRRC45","gene_name":"leucine rich repeat containing 45 [Source:HGNC Symbol;Acc:HGNC:28302]","synonyms":"MGC20806","biotype":"protein_coding","ncbi_id":"201255","summary":null,"start":82023302,"end":82031151,"strand":1,"description":"leucine rich repeat containing 45 [Source:HGNC Symbol;Acc:HGNC:28302]"}, {"versioned_ensembl_gene_id":"ENSG00000235296.1","gene_symbol":"AC145207.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81941869,"end":81947601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263585.1","gene_symbol":"AC145207.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81932398,"end":81933058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267670.1","gene_symbol":"AC022098.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14030855,"end":14031557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274226.5","gene_symbol":"TBC1D3H","gene_name":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729877","summary":null,"start":36377531,"end":36388423,"strand":-1,"description":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]"}, {"versioned_ensembl_gene_id":"ENSG00000234384.1","gene_symbol":"LINC01049","gene_name":"long intergenic non-protein coding RNA 1049 [Source:HGNC Symbol;Acc:HGNC:49043]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927224","summary":null,"start":90493287,"end":90535080,"strand":1,"description":"long intergenic non-protein coding RNA 1049 [Source:HGNC Symbol;Acc:HGNC:49043]"}, {"versioned_ensembl_gene_id":"ENSG00000133706.17","gene_symbol":"LARS","gene_name":"leucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6512]","synonyms":"RNTLS,LEUS,LARS1,HSPC192,FLJ21788,FLJ10595","biotype":"protein_coding","ncbi_id":"51520","summary":"This gene encodes a cytosolic leucine-tRNA synthetase, a member of the class I aminoacyl-tRNA synthetase family. The encoded enzyme catalyzes the ATP-dependent ligation of L-leucine to tRNA(Leu). It is found in the cytoplasm as part of a multisynthetase complex and interacts with the arginine tRNA synthetase through its C-terminal domain. A mutation in this gene was found in affected individuals with infantile liver failure syndrome 1. Alternatively spliced transcript variants of this gene have been observed. [provided by RefSeq, Dec 2015]","start":146113038,"end":146182660,"strand":-1,"description":"leucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6512]"}, {"versioned_ensembl_gene_id":"ENSG00000258672.1","gene_symbol":"AL160313.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99691445,"end":99693648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270294.1","gene_symbol":"XIAPP1","gene_name":"X-linked inhibitor of apoptosis pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996851","summary":null,"start":109680442,"end":109681041,"strand":1,"description":"X-linked inhibitor of apoptosis pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52375]"}, {"versioned_ensembl_gene_id":"ENSG00000268681.1","gene_symbol":"COX6CP7","gene_name":"cytochrome c oxidase subunit 6C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480265","summary":null,"start":49502432,"end":49502639,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49359]"}, {"versioned_ensembl_gene_id":"ENSG00000229775.6","gene_symbol":"AL353148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106140264,"end":106188722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198561.13","gene_symbol":"CTNND1","gene_name":"catenin delta 1 [Source:HGNC Symbol;Acc:HGNC:2515]","synonyms":"p120ctn,p120cas,p120,KIAA0384,CTNND","biotype":"protein_coding","ncbi_id":"1500","summary":"This gene encodes a member of the Armadillo protein family, which function in adhesion between cells and signal transduction. Multiple translation initiation codons and alternative splicing result in many different isoforms being translated. Not all of the full-length natures of the described transcript variants have been determined. Read-through transcription also exists between this gene and the neighboring upstream thioredoxin-related transmembrane protein 2 (TMX2) gene. [provided by RefSeq, Dec 2010]","start":57753243,"end":57819546,"strand":1,"description":"catenin delta 1 [Source:HGNC Symbol;Acc:HGNC:2515]"}, {"versioned_ensembl_gene_id":"ENSG00000250747.1","gene_symbol":"AC116345.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73152416,"end":73152938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226387.2","gene_symbol":"SORCS3-AS1","gene_name":"SORCS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45244]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505890","summary":null,"start":104664608,"end":104666200,"strand":-1,"description":"SORCS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45244]"}, {"versioned_ensembl_gene_id":"ENSG00000280070.1","gene_symbol":"AL049833.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96992864,"end":96996601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213128.3","gene_symbol":"AC109327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80542203,"end":80542605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262979.1","gene_symbol":"AC124319.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":80315651,"end":80316633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225748.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"BAT2,G2,D6S51E","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31697009,"end":31714058,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000181045.14","gene_symbol":"SLC26A11","gene_name":"solute carrier family 26 member 11 [Source:HGNC Symbol;Acc:HGNC:14471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284129","summary":"This gene encodes a member of the solute linked carrier 26 family of anion exchangers. Members of this family of proteins are essential for numerous cellular functions including homeostasis and intracellular electrolyte balance. The encoded protein is a sodium independent sulfate transporter that is sensitive to the anion exchanger inhibitor 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":80219699,"end":80253500,"strand":1,"description":"solute carrier family 26 member 11 [Source:HGNC Symbol;Acc:HGNC:14471]"}, {"versioned_ensembl_gene_id":"ENSG00000168676.10","gene_symbol":"KCTD19","gene_name":"potassium channel tetramerization domain containing 19 [Source:HGNC Symbol;Acc:HGNC:24753]","synonyms":"FLJ40162","biotype":"protein_coding","ncbi_id":"146212","summary":null,"start":67289428,"end":67326763,"strand":-1,"description":"potassium channel tetramerization domain containing 19 [Source:HGNC Symbol;Acc:HGNC:24753]"}, {"versioned_ensembl_gene_id":"ENSG00000141519.14","gene_symbol":"CCDC40","gene_name":"coiled-coil domain containing 40 [Source:HGNC Symbol;Acc:HGNC:26090]","synonyms":"CILD15,KIAA1640,FLJ32021,FLJ20753,FAP172","biotype":"protein_coding","ncbi_id":"55036","summary":"This gene encodes a protein that is necessary for motile cilia function. It functions in correct left-right axis formation by regulating the assembly of the inner dynein arm and the dynein regulatory complexes, which control ciliary beat. Mutations in this gene cause ciliary dyskinesia type 15, a disorder due to defects in cilia motility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":80036632,"end":80100613,"strand":1,"description":"coiled-coil domain containing 40 [Source:HGNC Symbol;Acc:HGNC:26090]"}, {"versioned_ensembl_gene_id":"ENSG00000163485.16","gene_symbol":"ADORA1","gene_name":"adenosine A1 receptor [Source:HGNC Symbol;Acc:HGNC:262]","synonyms":"RDC7","biotype":"protein_coding","ncbi_id":"134","summary":"The protein encoded by this gene is an adenosine receptor that belongs to the G-protein coupled receptor 1 family. There are 3 types of adenosine receptors, each with a specific pattern of ligand binding and tissue distribution, and together they regulate a diverse set of physiologic functions. The type A1 receptors inhibit adenylyl cyclase, and play a role in the fertilization process. Animal studies also suggest a role for A1 receptors in kidney function and ethanol intoxication. Transcript variants with alternative splicing in the 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]","start":203090654,"end":203167405,"strand":1,"description":"adenosine A1 receptor [Source:HGNC Symbol;Acc:HGNC:262]"}, {"versioned_ensembl_gene_id":"ENSG00000224671.2","gene_symbol":"AC105940.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203144694,"end":203152579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234775.1","gene_symbol":"AC105940.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203127259,"end":203127954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262172.1","gene_symbol":"AC116025.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79991944,"end":79992841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088038.17","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54137728,"end":54155681,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000223745.7","gene_symbol":"CCDC18-AS1","gene_name":"CCDC18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52262]","synonyms":"ENST00000440778.1","biotype":"processed_transcript","ncbi_id":"100131564","summary":null,"start":93262186,"end":93346025,"strand":-1,"description":"CCDC18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52262]"}, {"versioned_ensembl_gene_id":"ENSG00000206513.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555518,"end":29559832,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000278822.1","gene_symbol":"WT1-AS_1","gene_name":"WT1 antisense RNA conserved region 1 [Source:RFAM;Acc:RF02203]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32435738,"end":32435846,"strand":1,"description":"WT1 antisense RNA conserved region 1 [Source:RFAM;Acc:RF02203]"}, {"versioned_ensembl_gene_id":"ENSG00000136811.16","gene_symbol":"ODF2","gene_name":"outer dense fiber of sperm tails 2 [Source:HGNC Symbol;Acc:HGNC:8114]","synonyms":"ODF84,CT134","biotype":"protein_coding","ncbi_id":"4957","summary":"The outer dense fibers are cytoskeletal structures that surround the axoneme in the middle piece and principal piece of the sperm tail. The fibers function in maintaining the elastic structure and recoil of the sperm tail as well as in protecting the tail from shear forces during epididymal transport and ejaculation. Defects in the outer dense fibers lead to abnormal sperm morphology and infertility. This gene encodes one of the major outer dense fiber proteins. Alternative splicing results in multiple transcript variants. The longer transcripts, also known as 'Cenexins', encode proteins with a C-terminal extension that are differentially targeted to somatic centrioles and thought to be crucial for the formation of microtubule organizing centers. [provided by RefSeq, Oct 2010]","start":128455186,"end":128501292,"strand":1,"description":"outer dense fiber of sperm tails 2 [Source:HGNC Symbol;Acc:HGNC:8114]"}, {"versioned_ensembl_gene_id":"ENSG00000113578.17","gene_symbol":"FGF1","gene_name":"fibroblast growth factor 1 [Source:HGNC Symbol;Acc:HGNC:3665]","synonyms":"FGF-alpha,ECGFB,ECGFA,ECGF-beta,ECGF,AFGF,HBGF1,GLIO703,FGFA","biotype":"protein_coding","ncbi_id":"2246","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein functions as a modifier of endothelial cell migration and proliferation, as well as an angiogenic factor. It acts as a mitogen for a variety of mesoderm- and neuroectoderm-derived cells in vitro, thus is thought to be involved in organogenesis. Multiple alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Jan 2009]","start":142592178,"end":142698070,"strand":-1,"description":"fibroblast growth factor 1 [Source:HGNC Symbol;Acc:HGNC:3665]"}, {"versioned_ensembl_gene_id":"ENSG00000233330.1","gene_symbol":"AL078581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149591755,"end":149592663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231804.1","gene_symbol":"AL353748.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88484852,"end":88485325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232170.5","gene_symbol":"LINC00708","gene_name":"long intergenic non-protein coding RNA 708 [Source:HGNC Symbol;Acc:HGNC:44694]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507143","summary":null,"start":8259331,"end":8268305,"strand":-1,"description":"long intergenic non-protein coding RNA 708 [Source:HGNC Symbol;Acc:HGNC:44694]"}, {"versioned_ensembl_gene_id":"ENSG00000131013.3","gene_symbol":"PPIL4","gene_name":"peptidylprolyl isomerase like 4 [Source:HGNC Symbol;Acc:HGNC:15702]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85313","summary":"This gene is a member of the cyclophilin family of peptidylprolyl isomerases. The cyclophilins are a highly conserved family, members of which play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. [provided by RefSeq, Jul 2008]","start":149504733,"end":149546038,"strand":-1,"description":"peptidylprolyl isomerase like 4 [Source:HGNC Symbol;Acc:HGNC:15702]"}, {"versioned_ensembl_gene_id":"ENSG00000255292.7","gene_symbol":"SDHD","gene_name":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]","synonyms":"PGL,cybS,PGL1","biotype":"protein_coding","ncbi_id":"6392","summary":"This gene encodes a member of complex II of the respiratory chain, which is responsible for the oxidation of succinate. The encoded protein is one of two integral membrane proteins anchoring the complex to the matrix side of the mitochondrial inner membrane. Mutations in this gene are associated with the formation of tumors, including hereditary paraganglioma. Transmission of disease occurs almost exclusively through the paternal allele, suggesting that this locus may be maternally imprinted. There are pseudogenes for this gene on chromosomes 1, 2, 3, 7, and 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":112086824,"end":112193805,"strand":1,"description":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]"}, {"versioned_ensembl_gene_id":"ENSG00000220749.4","gene_symbol":"RPL21P28","gene_name":"ribosomal protein L21 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36258]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131205","summary":null,"start":212051524,"end":212052006,"strand":-1,"description":"ribosomal protein L21 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36258]"}, {"versioned_ensembl_gene_id":"ENSG00000267601.1","gene_symbol":"AC022966.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78855478,"end":78855844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267491.1","gene_symbol":"AC100788.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78903263,"end":78905024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108561.8","gene_symbol":"C1QBP","gene_name":"complement C1q binding protein [Source:HGNC Symbol;Acc:HGNC:1243]","synonyms":"SF2p32,p32,HABP1,gC1qR,gC1Q-R","biotype":"protein_coding","ncbi_id":"708","summary":"The human complement subcomponent C1q associates with C1r and C1s in order to yield the first component of the serum complement system. The protein encoded by this gene is known to bind to the globular heads of C1q molecules and inhibit C1 activation. This protein has also been identified as the p32 subunit of pre-mRNA splicing factor SF2, as well as a hyaluronic acid-binding protein. [provided by RefSeq, Jul 2008]","start":5432777,"end":5448830,"strand":-1,"description":"complement C1q binding protein [Source:HGNC Symbol;Acc:HGNC:1243]"}, {"versioned_ensembl_gene_id":"ENSG00000150768.15","gene_symbol":"DLAT","gene_name":"dihydrolipoamide S-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2896]","synonyms":"PDC-E2,DLTA","biotype":"protein_coding","ncbi_id":"1737","summary":"This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.[provided by RefSeq, Oct 2009]","start":112024814,"end":112064390,"strand":1,"description":"dihydrolipoamide S-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2896]"}, {"versioned_ensembl_gene_id":"ENSG00000253146.1","gene_symbol":"CIR1P1","gene_name":"corepressor interacting with RBPJ, 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131740","summary":null,"start":154559308,"end":154560440,"strand":-1,"description":"corepressor interacting with RBPJ, 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44011]"}, {"versioned_ensembl_gene_id":"ENSG00000113555.5","gene_symbol":"PCDH12","gene_name":"protocadherin 12 [Source:HGNC Symbol;Acc:HGNC:8657]","synonyms":"VE-cadherin-2","biotype":"protein_coding","ncbi_id":"51294","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 6 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene localizes to the region on chromosome 5 where the protocadherin gene clusters reside. The exon organization of this transcript is similar to that of the gene cluster transcripts, notably the first large exon, but no significant sequence homology exists. The function of this cellular adhesion protein is undetermined but mouse protocadherin 12 does not bind catenins and appears to have no affect on cell migration or growth. [provided by RefSeq, Jul 2008]","start":141943585,"end":141969741,"strand":-1,"description":"protocadherin 12 [Source:HGNC Symbol;Acc:HGNC:8657]"}, {"versioned_ensembl_gene_id":"ENSG00000270547.5","gene_symbol":"LINC01235","gene_name":"long intergenic non-protein coding RNA 1235 [Source:HGNC Symbol;Acc:HGNC:49769]","synonyms":"FLJ41200","biotype":"lincRNA","ncbi_id":"401492","summary":null,"start":13406380,"end":13433053,"strand":-1,"description":"long intergenic non-protein coding RNA 1235 [Source:HGNC Symbol;Acc:HGNC:49769]"}, {"versioned_ensembl_gene_id":"ENSG00000206519.3","gene_symbol":"BX000688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582427,"end":29582944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182704.7","gene_symbol":"TSKU","gene_name":"tsukushi, small leucine rich proteoglycan [Source:HGNC Symbol;Acc:HGNC:28850]","synonyms":"TSK,LRRC54,E2IG4","biotype":"protein_coding","ncbi_id":"25987","summary":null,"start":76782251,"end":76798154,"strand":1,"description":"tsukushi, small leucine rich proteoglycan [Source:HGNC Symbol;Acc:HGNC:28850]"}, {"versioned_ensembl_gene_id":"ENSG00000108669.16","gene_symbol":"CYTH1","gene_name":"cytohesin 1 [Source:HGNC Symbol;Acc:HGNC:9501]","synonyms":"PSCD1,D17S811E,cytohesin-1,B2-1","biotype":"protein_coding","ncbi_id":"9267","summary":"The protein encoded by this gene is a member of the PSCD family. Members of this family have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. This gene is highly expressed in natural killer and peripheral T cells, and regulates the adhesiveness of integrins at the plasma membrane of lymphocytes. A pseudogene of this gene has been defined on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":78674048,"end":78782297,"strand":-1,"description":"cytohesin 1 [Source:HGNC Symbol;Acc:HGNC:9501]"}, {"versioned_ensembl_gene_id":"ENSG00000279154.1","gene_symbol":"AL353726.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88177695,"end":88178578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101353.14","gene_symbol":"MROH8","gene_name":"maestro heat like repeat family member 8 [Source:HGNC Symbol;Acc:HGNC:16125]","synonyms":"dJ621N11.3,C20orf132,C20orf131,dJ621N11.4","biotype":"protein_coding","ncbi_id":"140699","summary":"The protein encoded by this gene belongs to the maestro heat-like repeat family. The exact function of this gene is not known, however, in a genome-wide association study using hippocampal atrophy as a quantitative trait, this gene has been associated with Alzheimer's disease (PMID:19668339). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":37101226,"end":37179588,"strand":-1,"description":"maestro heat like repeat family member 8 [Source:HGNC Symbol;Acc:HGNC:16125]"}, {"versioned_ensembl_gene_id":"ENSG00000230716.3","gene_symbol":"KRT8P7","gene_name":"keratin 8 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729131","summary":null,"start":119602875,"end":119604306,"strand":-1,"description":"keratin 8 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33361]"}, {"versioned_ensembl_gene_id":"ENSG00000099338.22","gene_symbol":"CATSPERG","gene_name":"cation channel sperm associated auxiliary subunit gamma [Source:HGNC Symbol;Acc:HGNC:25243]","synonyms":"FLJ46353,DKFZp434A1022,C19orf15","biotype":"protein_coding","ncbi_id":"57828","summary":"CATSPERG is a subunit of the CATSPER (see CATSPER1; MIM 606389) sperm calcium channel, which is required for sperm hyperactivated motility and male fertility (Wang et al., 2009 [PubMed 19516020]).[supplied by OMIM, Jul 2010]","start":38335775,"end":38370943,"strand":1,"description":"cation channel sperm associated auxiliary subunit gamma [Source:HGNC Symbol;Acc:HGNC:25243]"}, {"versioned_ensembl_gene_id":"ENSG00000187775.16","gene_symbol":"DNAH17","gene_name":"dynein axonemal heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]","synonyms":"FLJ40457,DNEL2,DNAHL1","biotype":"protein_coding","ncbi_id":"8632","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]","start":78423697,"end":78577394,"strand":-1,"description":"dynein axonemal heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]"}, {"versioned_ensembl_gene_id":"ENSG00000267166.5","gene_symbol":"AC007993.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43922775,"end":43927388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236146.2","gene_symbol":"AL353803.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129380136,"end":129380470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224307.1","gene_symbol":"AL161785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129282458,"end":129285728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204529.4","gene_symbol":"GUCY2EP","gene_name":"guanylate cyclase 2E, pseudogene [Source:HGNC Symbol;Acc:HGNC:4690]","synonyms":"GUCY2E,GC-E","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390226","summary":"This olfactory specific guanylyl cyclase is part of the mammalian olfactory system and and encodes a protein involved in chemosensation in rodents. The gene has become inactivated to become a pseudogene is humans and most primates. [provided by RefSeq, Oct 2008]","start":76694041,"end":76719801,"strand":-1,"description":"guanylate cyclase 2E, pseudogene [Source:HGNC Symbol;Acc:HGNC:4690]"}, {"versioned_ensembl_gene_id":"ENSG00000075388.3","gene_symbol":"FGF4","gene_name":"fibroblast growth factor 4 [Source:HGNC Symbol;Acc:HGNC:3682]","synonyms":"KFGF,K-FGF,HSTF1,HST-1,HST,HBGF-4","biotype":"protein_coding","ncbi_id":"2249","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its oncogenic transforming activity. This gene and FGF3, another oncogenic growth factor, are located closely on chromosome 11. Co-amplification of both genes was found in various kinds of human tumors. Studies on the mouse homolog suggested a function in bone morphogenesis and limb development through the sonic hedgehog (SHH) signaling pathway. [provided by RefSeq, Jul 2008]","start":69771016,"end":69775403,"strand":-1,"description":"fibroblast growth factor 4 [Source:HGNC Symbol;Acc:HGNC:3682]"}, {"versioned_ensembl_gene_id":"ENSG00000217824.1","gene_symbol":"SNRPEP6","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43571]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874414","summary":null,"start":148567378,"end":148567654,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43571]"}, {"versioned_ensembl_gene_id":"ENSG00000268707.1","gene_symbol":"AL158151.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129170434,"end":129170940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188483.7","gene_symbol":"IER5L","gene_name":"immediate early response 5 like [Source:HGNC Symbol;Acc:HGNC:23679]","synonyms":"bA247A12.2","biotype":"protein_coding","ncbi_id":"389792","summary":null,"start":129175552,"end":129178262,"strand":-1,"description":"immediate early response 5 like [Source:HGNC Symbol;Acc:HGNC:23679]"}, {"versioned_ensembl_gene_id":"ENSG00000277797.1","gene_symbol":"AL359693.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81551686,"end":81554092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258703.1","gene_symbol":"AL161757.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56759379,"end":56765757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143774.16","gene_symbol":"GUK1","gene_name":"guanylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:4693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2987","summary":"The protein encoded by this gene is an enzyme that catalyzes the transfer of a phosphate group from ATP to guanosine monophosphate (GMP) to form guanosine diphosphate (GDP). The encoded protein is thought to be a good target for cancer chemotherapy. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":228139962,"end":228148984,"strand":1,"description":"guanylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:4693]"}, {"versioned_ensembl_gene_id":"ENSG00000250194.1","gene_symbol":"AC109458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125074665,"end":125074980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249365.1","gene_symbol":"AC110009.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125108204,"end":125149929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253310.1","gene_symbol":"IGHVIII-76-1","gene_name":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]","synonyms":"IGHV(III)-76-1","biotype":"IG_V_pseudogene","ncbi_id":"28339","summary":null,"start":106831767,"end":106832052,"strand":-1,"description":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]"}, {"versioned_ensembl_gene_id":"ENSG00000260066.1","gene_symbol":"AC112176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1725149,"end":1728172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167874.6","gene_symbol":"TMEM88","gene_name":"transmembrane protein 88 [Source:HGNC Symbol;Acc:HGNC:32371]","synonyms":"MGC71744,FLJ20025","biotype":"protein_coding","ncbi_id":"92162","summary":null,"start":7855065,"end":7856099,"strand":1,"description":"transmembrane protein 88 [Source:HGNC Symbol;Acc:HGNC:32371]"}, {"versioned_ensembl_gene_id":"ENSG00000118495.18","gene_symbol":"PLAGL1","gene_name":"PLAG1 like zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:9046]","synonyms":"ZAC,LOT1","biotype":"protein_coding","ncbi_id":"5325","summary":"This gene encodes a C2H2 zinc finger protein that functions as a suppressor of cell growth. This gene is often deleted or methylated and silenced in cancer cells. In addition, overexpression of this gene during fetal development is thought to be the causal factor for transient neonatal diabetes mellitus (TNDM). Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding two different protein isoforms. The P1 downstream promoter of this gene is imprinted, with preferential expression from the paternal allele in many tissues. [provided by RefSeq, Nov 2015]","start":143940300,"end":144064599,"strand":-1,"description":"PLAG1 like zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:9046]"}, {"versioned_ensembl_gene_id":"ENSG00000265168.1","gene_symbol":"AC005726.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28573117,"end":28574243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211456.10","gene_symbol":"SACM1L","gene_name":"SAC1 like phosphatidylinositide phosphatase [Source:HGNC Symbol;Acc:HGNC:17059]","synonyms":"SAC1,KIAA0851","biotype":"protein_coding","ncbi_id":"22908","summary":"This gene encodes an integral membrane protein, which is localized to the endoplasmic reticulum, and functions as a phosphoinositide phosphatase that hydrolyzes phosphatidylinositol 3-phosphate, phosphatidylinositol 4-phosphate, and phosphatidylinositol 3,5-bisphosphate. Deletion of this gene in mouse results in preimplantation lethality. Other studies suggest that this gene is also involved in the organization of golgi membranes and mitotic spindles. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame, downstream translation termination codon via a stop codon readthrough mechanism.[provided by RefSeq, Dec 2017]","start":45689056,"end":45745424,"strand":1,"description":"SAC1 like phosphatidylinositide phosphatase [Source:HGNC Symbol;Acc:HGNC:17059]"}, {"versioned_ensembl_gene_id":"ENSG00000167941.2","gene_symbol":"SOST","gene_name":"sclerostin [Source:HGNC Symbol;Acc:HGNC:13771]","synonyms":"VBCH,DAND6","biotype":"protein_coding","ncbi_id":"50964","summary":"Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease. [provided by RefSeq, Jul 2008]","start":43753731,"end":43758788,"strand":-1,"description":"sclerostin [Source:HGNC Symbol;Acc:HGNC:13771]"}, {"versioned_ensembl_gene_id":"ENSG00000258784.1","gene_symbol":"AL355773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55748208,"end":55773203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104901.6","gene_symbol":"DKKL1","gene_name":"dickkopf like acrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:16528]","synonyms":"SGY-1,CT34","biotype":"protein_coding","ncbi_id":"27120","summary":"The dickkopf protein family interacts with the Wnt signaling pathway and its members are characterized by two conserved cysteine-rich domains. This gene encodes a secreted protein that has low sequence similarity to the dickkopf-3 protein. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":49361783,"end":49375116,"strand":1,"description":"dickkopf like acrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:16528]"}, {"versioned_ensembl_gene_id":"ENSG00000134940.13","gene_symbol":"ACRV1","gene_name":"acrosomal vesicle protein 1 [Source:HGNC Symbol;Acc:HGNC:127]","synonyms":"SP-10,D11S4365,SPACA2","biotype":"protein_coding","ncbi_id":"56","summary":"This gene encodes a testis-specific, differentiation antigen, acrosomal vesicle protein 1, that arises within the acrosomal vesicle during spermatogenesis, and is associated with the acrosomal membranes and matrix of mature sperm. The acrosomal vesicle protein 1 may be involved in sperm-zona binding or penetration. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]","start":125671522,"end":125681123,"strand":-1,"description":"acrosomal vesicle protein 1 [Source:HGNC Symbol;Acc:HGNC:127]"}, {"versioned_ensembl_gene_id":"ENSG00000109814.11","gene_symbol":"UGDH","gene_name":"UDP-glucose 6-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7358","summary":"The protein encoded by this gene converts UDP-glucose to UDP-glucuronate and thereby participates in the biosynthesis of glycosaminoglycans such as hyaluronan, chondroitin sulfate, and heparan sulfate. These glycosylated compounds are common components of the extracellular matrix and likely play roles in signal transduction, cell migration, and cancer growth and metastasis. The expression of this gene is up-regulated by transforming growth factor beta and down-regulated by hypoxia. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":39498755,"end":39528311,"strand":-1,"description":"UDP-glucose 6-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12525]"}, {"versioned_ensembl_gene_id":"ENSG00000196344.11","gene_symbol":"ADH7","gene_name":"alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [Source:HGNC Symbol;Acc:HGNC:256]","synonyms":"ADH-4","biotype":"protein_coding","ncbi_id":"131","summary":"This gene encodes class IV alcohol dehydrogenase 7 mu or sigma subunit, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. The enzyme encoded by this gene is inefficient in ethanol oxidation, but is the most active as a retinol dehydrogenase; thus it may participate in the synthesis of retinoic acid, a hormone important for cellular differentiation. The expression of this gene is much more abundant in stomach than liver, thus differing from the other known gene family members. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":99412261,"end":99435737,"strand":-1,"description":"alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [Source:HGNC Symbol;Acc:HGNC:256]"}, {"versioned_ensembl_gene_id":"ENSG00000186652.9","gene_symbol":"PRG2","gene_name":"proteoglycan 2, pro eosinophil major basic protein [Source:HGNC Symbol;Acc:HGNC:9362]","synonyms":"proMBP,MBP,BMPG","biotype":"protein_coding","ncbi_id":"5553","summary":"The protein encoded by this gene is the predominant constituent of the crystalline core of the eosinophil granule. High levels of the proform of this protein are also present in placenta and pregnancy serum, where it exists as a complex with several other proteins including pregnancy-associated plasma protein A (PAPPA), angiotensinogen (AGT), and C3dg. This protein may be involved in antiparasitic defense mechanisms as a cytotoxin and helminthotoxin, and in immune hypersensitivity reactions. The encoded protein contains a peptide that displays potent antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi. It is directly implicated in epithelial cell damage, exfoliation, and bronchospasm in allergic diseases. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":57386794,"end":57390657,"strand":-1,"description":"proteoglycan 2, pro eosinophil major basic protein [Source:HGNC Symbol;Acc:HGNC:9362]"}, {"versioned_ensembl_gene_id":"ENSG00000267508.5","gene_symbol":"ZNF285","gene_name":"zinc finger protein 285 [Source:HGNC Symbol;Acc:HGNC:13079]","synonyms":"ZNF285A","biotype":"protein_coding","ncbi_id":"26974","summary":null,"start":44382298,"end":44401608,"strand":-1,"description":"zinc finger protein 285 [Source:HGNC Symbol;Acc:HGNC:13079]"}, {"versioned_ensembl_gene_id":"ENSG00000198453.12","gene_symbol":"ZNF568","gene_name":"zinc finger protein 568 [Source:HGNC Symbol;Acc:HGNC:25392]","synonyms":"DKFZp686B0797","biotype":"protein_coding","ncbi_id":"374900","summary":null,"start":36916329,"end":36998700,"strand":1,"description":"zinc finger protein 568 [Source:HGNC Symbol;Acc:HGNC:25392]"}, {"versioned_ensembl_gene_id":"ENSG00000162851.7","gene_symbol":"TFB2M","gene_name":"transcription factor B2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:18559]","synonyms":"Hkp1,FLJ23182,FLJ22661","biotype":"protein_coding","ncbi_id":"64216","summary":null,"start":246540560,"end":246566324,"strand":-1,"description":"transcription factor B2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:18559]"}, {"versioned_ensembl_gene_id":"ENSG00000278077.1","gene_symbol":"AL591926.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41644771,"end":41644981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254851.1","gene_symbol":"AP005018.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":117135528,"end":117138582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153395.9","gene_symbol":"LPCAT1","gene_name":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]","synonyms":"FLJ12443,AYTL2,AGPAT9,AGPAT10","biotype":"protein_coding","ncbi_id":"79888","summary":"This gene encodes a member of the 1-acyl-sn-glycerol-3-phosphate acyltransferase family of proteins. The encoded enzyme plays a role in phospholipid metabolism, specifically in the conversion of lysophosphatidylcholine to phosphatidylcholine in the presence of acyl-CoA. This process is important in the synthesis of lung surfactant and platelet-activating factor (PAF). Elevated expression of this gene may contribute to the progression of oral squamous cell, prostate, breast, and other human cancers. [provided by RefSeq, Sep 2016]","start":1456480,"end":1523977,"strand":-1,"description":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]"}, {"versioned_ensembl_gene_id":"ENSG00000222206.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27223319,"end":27223427,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280735.1","gene_symbol":"AC217779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46062345,"end":46062802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226257.9","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31953357,"end":31965001,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000131504.15","gene_symbol":"DIAPH1","gene_name":"diaphanous related formin 1 [Source:HGNC Symbol;Acc:HGNC:2876]","synonyms":"LFHL1,hDIA1,DFNA1","biotype":"protein_coding","ncbi_id":"1729","summary":"This gene is a homolog of the Drosophila diaphanous gene, and has been linked to autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive low-frequency hearing loss. Actin polymerization involves proteins known to interact with diaphanous protein in Drosophila and mouse. It has therefore been speculated that this gene may have a role in the regulation of actin polymerization in hair cells of the inner ear. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":141515016,"end":141619055,"strand":-1,"description":"diaphanous related formin 1 [Source:HGNC Symbol;Acc:HGNC:2876]"}, {"versioned_ensembl_gene_id":"ENSG00000211962.2","gene_symbol":"IGHV1-46","gene_name":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28465","summary":null,"start":106511117,"end":106511856,"strand":-1,"description":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]"}, {"versioned_ensembl_gene_id":"ENSG00000253465.1","gene_symbol":"IGHVIV-44-1","gene_name":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]","synonyms":"IGHV(IV)-44-1","biotype":"IG_V_pseudogene","ncbi_id":"28337","summary":null,"start":106489345,"end":106489756,"strand":-1,"description":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]"}, {"versioned_ensembl_gene_id":"ENSG00000268818.2","gene_symbol":"AL049747.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35626988,"end":35635134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269994.1","gene_symbol":"AL513318.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87008455,"end":87042126,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268582.1","gene_symbol":"AC243960.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41652676,"end":41652963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235722.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30104215,"end":30107221,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000268997.1","gene_symbol":"DNAJC19P3","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861443","summary":null,"start":41638569,"end":41638899,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]"}, {"versioned_ensembl_gene_id":"ENSG00000253622.1","gene_symbol":"AC027419.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":117128455,"end":117130299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172900.12","gene_symbol":"FLJ42102","gene_name":"uncharacterized LOC399923 [Source:NCBI gene;Acc:399923]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"399923","summary":null,"start":71382601,"end":71423423,"strand":-1,"description":"uncharacterized LOC399923 [Source:NCBI gene;Acc:399923]"}, {"versioned_ensembl_gene_id":"ENSG00000213433.5","gene_symbol":"AC091982.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":151765859,"end":151766378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125898.12","gene_symbol":"FAM110A","gene_name":"family with sequence similarity 110 member A [Source:HGNC Symbol;Acc:HGNC:16188]","synonyms":"C20orf55,bA371L19.3","biotype":"protein_coding","ncbi_id":"83541","summary":null,"start":833715,"end":857463,"strand":1,"description":"family with sequence similarity 110 member A [Source:HGNC Symbol;Acc:HGNC:16188]"}, {"versioned_ensembl_gene_id":"ENSG00000167881.14","gene_symbol":"SRP68","gene_name":"signal recognition particle 68 [Source:HGNC Symbol;Acc:HGNC:11302]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6730","summary":"This gene encodes a subunit of the signal recognition particle (SRP). The SRP is a ribonucleoprotein complex that transports secreted and membrane proteins to the endoplasmic reticulum for processing. The complex includes a 7S RNA and six protein subunits. The encoded protein is the 68kDa component of the SRP, and forms a heterodimer with the 72kDa subunit that is required for SRP function. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and three pseudogenes of this gene are located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, May 2012]","start":76038775,"end":76072653,"strand":-1,"description":"signal recognition particle 68 [Source:HGNC Symbol;Acc:HGNC:11302]"}, {"versioned_ensembl_gene_id":"ENSG00000278259.4","gene_symbol":"MYO19","gene_name":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]","synonyms":"MYOHD1,FLJ22865","biotype":"protein_coding","ncbi_id":"80179","summary":null,"start":36495633,"end":36543435,"strand":-1,"description":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]"}, {"versioned_ensembl_gene_id":"ENSG00000226812.2","gene_symbol":"AL117382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44347552,"end":44355185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269292.1","gene_symbol":"AC093503.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46609277,"end":46610779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101074.3","gene_symbol":"R3HDML","gene_name":"R3H domain containing like [Source:HGNC Symbol;Acc:HGNC:16249]","synonyms":"dJ881L22.3","biotype":"protein_coding","ncbi_id":"140902","summary":null,"start":44336986,"end":44351235,"strand":1,"description":"R3H domain containing like [Source:HGNC Symbol;Acc:HGNC:16249]"}, {"versioned_ensembl_gene_id":"ENSG00000272479.1","gene_symbol":"AC010857.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40519565,"end":40520158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255321.1","gene_symbol":"AC068389.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60551957,"end":60553036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118492.16","gene_symbol":"ADGB","gene_name":"androglobin [Source:HGNC Symbol;Acc:HGNC:21212]","synonyms":"FLJ23121,dJ408K24.1,CAPN16,C6orf103","biotype":"protein_coding","ncbi_id":"79747","summary":null,"start":146598965,"end":146815462,"strand":1,"description":"androglobin [Source:HGNC Symbol;Acc:HGNC:21212]"}, {"versioned_ensembl_gene_id":"ENSG00000280014.1","gene_symbol":"AC243960.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41551568,"end":41552274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160294.10","gene_symbol":"MCM3AP","gene_name":"minichromosome maintenance complex component 3 associated protein [Source:HGNC Symbol;Acc:HGNC:6946]","synonyms":"SAC3,Map80,KIAA0572,GANP","biotype":"protein_coding","ncbi_id":"8888","summary":"The minichromosome maintenance protein 3 (MCM3) is one of the MCM proteins essential for the initiation of DNA replication. The protein encoded by this gene is a MCM3 binding protein. It was reported to have phosphorylation-dependent DNA-primase activity, which was up-regulated in antigen immunization induced germinal center. This protein was demonstrated to be an acetyltransferase that acetylates MCM3 and plays a role in DNA replication. The mutagenesis of a nuclear localization signal of MCM3 affects the binding of this protein with MCM3, suggesting that this protein may also facilitate MCM3 nuclear localization. This gene is expressed in the brain or in neuronal tissue. An allelic variant encoding amino acid Lys at 915, instead of conserved Glu, has been identified in patients with mild intellectual disability. [provided by RefSeq, Jan 2014]","start":46235126,"end":46286297,"strand":-1,"description":"minichromosome maintenance complex component 3 associated protein [Source:HGNC Symbol;Acc:HGNC:6946]"}, {"versioned_ensembl_gene_id":"ENSG00000174788.9","gene_symbol":"PCP2","gene_name":"Purkinje cell protein 2 [Source:HGNC Symbol;Acc:HGNC:30209]","synonyms":"MGC41903,GPSM4","biotype":"protein_coding","ncbi_id":"126006","summary":null,"start":7631611,"end":7633748,"strand":-1,"description":"Purkinje cell protein 2 [Source:HGNC Symbol;Acc:HGNC:30209]"}, {"versioned_ensembl_gene_id":"ENSG00000226009.1","gene_symbol":"KCNIP2-AS1","gene_name":"KCNIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48680]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289509","summary":null,"start":101819078,"end":101828779,"strand":1,"description":"KCNIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48680]"}, {"versioned_ensembl_gene_id":"ENSG00000185420.18","gene_symbol":"SMYD3","gene_name":"SET and MYND domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15513]","synonyms":"ZNFN3A1,ZMYND1,KMT3E","biotype":"protein_coding","ncbi_id":"64754","summary":"This gene encodes a histone methyltransferase which functions in RNA polymerase II complexes by an interaction with a specific RNA helicase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":245749342,"end":246507312,"strand":-1,"description":"SET and MYND domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15513]"}, {"versioned_ensembl_gene_id":"ENSG00000103353.15","gene_symbol":"UBFD1","gene_name":"ubiquitin family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30565]","synonyms":"UBPH,FLJ42145,FLJ38870","biotype":"protein_coding","ncbi_id":"56061","summary":null,"start":23557362,"end":23574389,"strand":1,"description":"ubiquitin family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30565]"}, {"versioned_ensembl_gene_id":"ENSG00000212240.1","gene_symbol":"RNU6-930P","gene_name":"RNA, U6 small nuclear 930, pseudogene [Source:HGNC Symbol;Acc:HGNC:47893]","synonyms":"RNU6-1173P","biotype":"snRNA","ncbi_id":"106480622","summary":null,"start":28915645,"end":28915744,"strand":1,"description":"RNA, U6 small nuclear 930, pseudogene [Source:HGNC Symbol;Acc:HGNC:47893]"}, {"versioned_ensembl_gene_id":"ENSG00000130528.11","gene_symbol":"HRC","gene_name":"histidine rich calcium binding protein [Source:HGNC Symbol;Acc:HGNC:5178]","synonyms":"MGC133236","biotype":"protein_coding","ncbi_id":"3270","summary":"This gene encodes a luminal sarcoplasmic reticulum protein identified by its ability to bind low-density lipoprotein with high affinity. The protein interacts with the cytoplasmic domain of triadin, the main transmembrane protein of the junctional sarcoplasmic reticulum (SR) of skeletal muscle. The protein functions in the regulation of releasable calcium into the SR. [provided by RefSeq, Sep 2008]","start":49151198,"end":49155424,"strand":-1,"description":"histidine rich calcium binding protein [Source:HGNC Symbol;Acc:HGNC:5178]"}, {"versioned_ensembl_gene_id":"ENSG00000233712.1","gene_symbol":"AL135929.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157636300,"end":157640301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279348.1","gene_symbol":"AC012513.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":216211404,"end":216213519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257272.1","gene_symbol":"AL162311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35873857,"end":35875303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254954.1","gene_symbol":"SLC2A13P1","gene_name":"SLC2A13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480239","summary":null,"start":60141821,"end":60142142,"strand":1,"description":"SLC2A13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48929]"}, {"versioned_ensembl_gene_id":"ENSG00000282887.2","gene_symbol":"AL358215.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110472543,"end":110474980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283999.1","gene_symbol":"AL358215.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110473756,"end":110488663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250161.1","gene_symbol":"TRMT112P5","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44024]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480784","summary":null,"start":139845078,"end":139845411,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44024]"}, {"versioned_ensembl_gene_id":"ENSG00000240194.7","gene_symbol":"CYMP","gene_name":"chymosin pseudogene [Source:HGNC Symbol;Acc:HGNC:2588]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"643160","summary":null,"start":110480752,"end":110491277,"strand":1,"description":"chymosin pseudogene [Source:HGNC Symbol;Acc:HGNC:2588]"}, {"versioned_ensembl_gene_id":"ENSG00000260581.1","gene_symbol":"AC011374.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151652275,"end":151655449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270380.1","gene_symbol":"AL358215.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110456505,"end":110457354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254045.1","gene_symbol":"IGHVIII-22-2","gene_name":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]","synonyms":"IGHV(III)-22-2","biotype":"IG_V_pseudogene","ncbi_id":"28349","summary":null,"start":106264688,"end":106264715,"strand":-1,"description":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]"}, {"versioned_ensembl_gene_id":"ENSG00000103855.17","gene_symbol":"CD276","gene_name":"CD276 molecule [Source:HGNC Symbol;Acc:HGNC:19137]","synonyms":"B7-H3,B7RP-2,B7H3","biotype":"protein_coding","ncbi_id":"80381","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily, and thought to participate in the regulation of T-cell-mediated immune response. Studies show that while the transcript of this gene is ubiquitously expressed in normal tissues and solid tumors, the protein is preferentially expressed only in tumor tissues. Additionally, it was observed that the 3' UTR of this transcript contains a target site for miR29 microRNA, and there is an inverse correlation between the expression of this protein and miR29 levels, suggesting regulation of expression of this gene product by miR29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":73683966,"end":73714518,"strand":1,"description":"CD276 molecule [Source:HGNC Symbol;Acc:HGNC:19137]"}, {"versioned_ensembl_gene_id":"ENSG00000258224.1","gene_symbol":"AC090049.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91871122,"end":91871230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235910.1","gene_symbol":"APOA1-AS","gene_name":"APOA1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40079]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104326055","summary":null,"start":116836117,"end":116855729,"strand":1,"description":"APOA1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40079]"}, {"versioned_ensembl_gene_id":"ENSG00000261268.1","gene_symbol":"AC112236.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139618136,"end":139623232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251455.1","gene_symbol":"AC092611.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151674483,"end":151677893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006071.12","gene_symbol":"ABCC8","gene_name":"ATP binding cassette subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:59]","synonyms":"TNDM2,SUR1,SUR,PHHI,MRP8,HRINS,HI,HHF1,ABC36","biotype":"protein_coding","ncbi_id":"6833","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations in the ABCC8 gene and deficiencies in the encoded protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2020]","start":17392885,"end":17476845,"strand":-1,"description":"ATP binding cassette subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:59]"}, {"versioned_ensembl_gene_id":"ENSG00000235687.9","gene_symbol":"LINC00993","gene_name":"long intergenic non-protein coding RNA 993 [Source:HGNC Symbol;Acc:HGNC:48948]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101929520","summary":null,"start":37248118,"end":37347031,"strand":1,"description":"long intergenic non-protein coding RNA 993 [Source:HGNC Symbol;Acc:HGNC:48948]"}, {"versioned_ensembl_gene_id":"ENSG00000197324.8","gene_symbol":"LRP10","gene_name":"LDL receptor related protein 10 [Source:HGNC Symbol;Acc:HGNC:14553]","synonyms":"MSTP087,MST087,MGC8675,LRP9,DKFZP564C1940","biotype":"protein_coding","ncbi_id":"26020","summary":"This gene encodes a low density lipoprotein receptor family protein. A similar protein in mouse is thought to play a role in the uptake of apolipoprotein E-containing lipoproteins. [provided by RefSeq, Jul 2016]","start":22871613,"end":22881580,"strand":1,"description":"LDL receptor related protein 10 [Source:HGNC Symbol;Acc:HGNC:14553]"}, {"versioned_ensembl_gene_id":"ENSG00000237970.1","gene_symbol":"TMEM161BP1","gene_name":"transmembrane protein 161B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646360","summary":null,"start":37337415,"end":37338871,"strand":1,"description":"transmembrane protein 161B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44973]"}, {"versioned_ensembl_gene_id":"ENSG00000101166.15","gene_symbol":"PRELID3B","gene_name":"PRELI domain containing 3B [Source:HGNC Symbol;Acc:HGNC:15892]","synonyms":"SLMO2,dJ543J19.5,C20orf45","biotype":"protein_coding","ncbi_id":"51012","summary":null,"start":59033145,"end":59042909,"strand":-1,"description":"PRELI domain containing 3B [Source:HGNC Symbol;Acc:HGNC:15892]"}, {"versioned_ensembl_gene_id":"ENSG00000122133.16","gene_symbol":"PAEP","gene_name":"progestagen associated endometrial protein [Source:HGNC Symbol;Acc:HGNC:8573]","synonyms":"PAEG,MGC142288,MGC138509,GdS,GdF,GdA,GD,PP14,PEP","biotype":"protein_coding","ncbi_id":"5047","summary":"This gene is a member of the kernel lipocalin superfamily whose members share relatively low sequence similarity but have highly conserved exon/intron structure and three-dimensional protein folding. Most lipocalins are clustered on the long arm of chromosome 9. The encoded glycoprotein has been previously referred to as pregnancy-associated endometrial alpha-2-globulin, placental protein 14, and glycodelin, but has been officially named progestagen-associated endometrial protein. Three distinct forms, with identical protein backbones but different glycosylation profiles, are found in amniotic fluid, follicular fluid and seminal plasma of the reproductive system. These glycoproteins have distinct and essential roles in regulating a uterine environment suitable for pregnancy and in the timing and occurrence of the appropriate sequence of events in the fertilization process. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":135561756,"end":135566955,"strand":1,"description":"progestagen associated endometrial protein [Source:HGNC Symbol;Acc:HGNC:8573]"}, {"versioned_ensembl_gene_id":"ENSG00000240303.7","gene_symbol":"ACAD11","gene_name":"acyl-CoA dehydrogenase family member 11 [Source:HGNC Symbol;Acc:HGNC:30211]","synonyms":"FLJ12592","biotype":"protein_coding","ncbi_id":"84129","summary":"This gene encodes an acyl-CoA dehydrogenase enzyme with a preference for carbon chain lengths between 20 and 26. Naturally occurring read-through transcription occurs between the upstream gene NPHP3 (nephronophthisis 3 (adolescent)) and this gene. [provided by RefSeq, Aug 2015]","start":132558138,"end":132660723,"strand":-1,"description":"acyl-CoA dehydrogenase family member 11 [Source:HGNC Symbol;Acc:HGNC:30211]"}, {"versioned_ensembl_gene_id":"ENSG00000101134.11","gene_symbol":"DOK5","gene_name":"docking protein 5 [Source:HGNC Symbol;Acc:HGNC:16173]","synonyms":"dJ805C22.1,C20orf180","biotype":"protein_coding","ncbi_id":"55816","summary":"The protein encoded by this gene is a member of the DOK family of membrane proteins, which are adapter proteins involved in signal transduction. The encoded protein interacts with phosphorylated receptor tyrosine kinases to mediate neurite outgrowth and activation of the MAP kinase pathway. Unlike other DOK family proteins, this protein does not interact with RASGAP. This protein is up-regulated in patients with systemic sclerosis and is associated with fibrosis induced by insulin-like growth factor binding protein 5. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":54475597,"end":54651171,"strand":1,"description":"docking protein 5 [Source:HGNC Symbol;Acc:HGNC:16173]"}, {"versioned_ensembl_gene_id":"ENSG00000238276.5","gene_symbol":"AL354863.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":118241564,"end":118267710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250948.1","gene_symbol":"AC091180.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49375380,"end":49380094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234715.1","gene_symbol":"AC005064.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103445207,"end":103514007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278861.1","gene_symbol":"AC117503.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123655528,"end":123656128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267022.1","gene_symbol":"AC067968.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":44025354,"end":44087318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222009.8","gene_symbol":"BTBD19","gene_name":"BTB domain containing 19 [Source:HGNC Symbol;Acc:HGNC:27145]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149478","summary":null,"start":44808482,"end":44815585,"strand":1,"description":"BTB domain containing 19 [Source:HGNC Symbol;Acc:HGNC:27145]"}, {"versioned_ensembl_gene_id":"ENSG00000262154.1","gene_symbol":"EIF1P4","gene_name":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130566","summary":null,"start":2822659,"end":2822993,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]"}, {"versioned_ensembl_gene_id":"ENSG00000275423.1","gene_symbol":"AC092650.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47989625,"end":47990526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204438.10","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31661229,"end":31666283,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000204956.5","gene_symbol":"PCDHGA1","gene_name":"protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:HGNC:8696]","synonyms":"PCDH-GAMMA-A1","biotype":"protein_coding","ncbi_id":"56114","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141330571,"end":141512981,"strand":1,"description":"protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:HGNC:8696]"}, {"versioned_ensembl_gene_id":"ENSG00000213140.3","gene_symbol":"ELK2AP","gene_name":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]","synonyms":"ELK2P1,ELK2.1,ELK2","biotype":"processed_pseudogene","ncbi_id":"2003","summary":null,"start":105672308,"end":105673314,"strand":-1,"description":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]"}, {"versioned_ensembl_gene_id":"ENSG00000107560.10","gene_symbol":"RAB11FIP2","gene_name":"RAB11 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29152]","synonyms":"Rab11-FIP2,nRip11,KIAA0941","biotype":"protein_coding","ncbi_id":"22841","summary":null,"start":118004916,"end":118046603,"strand":-1,"description":"RAB11 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29152]"}, {"versioned_ensembl_gene_id":"ENSG00000119686.9","gene_symbol":"FLVCR2","gene_name":"feline leukemia virus subgroup C cellular receptor family member 2 [Source:HGNC Symbol;Acc:HGNC:20105]","synonyms":"MFSD7C,FLJ20371,C14orf58","biotype":"protein_coding","ncbi_id":"55640","summary":"This gene encodes a member of the major facilitator superfamily. The encoded transmembrane protein is a calcium transporter. Unlike the related protein feline leukemia virus subgroup C receptor 1, the protein encoded by this locus does not bind to feline leukemia virus subgroup C envelope protein. The encoded protein may play a role in development of brain vascular endothelial cells, as mutations at this locus have been associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Aug 2010]","start":75578617,"end":75663214,"strand":1,"description":"feline leukemia virus subgroup C cellular receptor family member 2 [Source:HGNC Symbol;Acc:HGNC:20105]"}, {"versioned_ensembl_gene_id":"ENSG00000279191.1","gene_symbol":"AC068491.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":111321433,"end":111324812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242180.3","gene_symbol":"OR51B5","gene_name":"olfactory receptor family 51 subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:19599]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282763","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5342586,"end":5343524,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:19599]"}, {"versioned_ensembl_gene_id":"ENSG00000131437.15","gene_symbol":"KIF3A","gene_name":"kinesin family member 3A [Source:HGNC Symbol;Acc:HGNC:6319]","synonyms":"KLP-20,FLA10","biotype":"protein_coding","ncbi_id":"11127","summary":null,"start":132692628,"end":132737638,"strand":-1,"description":"kinesin family member 3A [Source:HGNC Symbol;Acc:HGNC:6319]"}, {"versioned_ensembl_gene_id":"ENSG00000236881.1","gene_symbol":"BX005428.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720705,"end":29721695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261308.2","gene_symbol":"FIGNL2","gene_name":"fidgetin like 2 [Source:HGNC Symbol;Acc:HGNC:13287]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401720","summary":null,"start":51817840,"end":51848766,"strand":-1,"description":"fidgetin like 2 [Source:HGNC Symbol;Acc:HGNC:13287]"}, {"versioned_ensembl_gene_id":"ENSG00000165802.22","gene_symbol":"NSMF","gene_name":"NMDA receptor synaptonuclear signaling and neuronal migration factor [Source:HGNC Symbol;Acc:HGNC:29843]","synonyms":"NELF","biotype":"protein_coding","ncbi_id":"26012","summary":"The protein encoded by this gene is involved in guidance of olfactory axon projections and migration of luteinizing hormone-releasing hormone neurons. Defects in this gene are a cause of idiopathic hypogonadotropic hypogonadism (IHH). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":137447573,"end":137459334,"strand":-1,"description":"NMDA receptor synaptonuclear signaling and neuronal migration factor [Source:HGNC Symbol;Acc:HGNC:29843]"}, {"versioned_ensembl_gene_id":"ENSG00000213619.9","gene_symbol":"NDUFS3","gene_name":"NADH:ubiquinone oxidoreductase core subunit S3 [Source:HGNC Symbol;Acc:HGNC:7710]","synonyms":"CI-30","biotype":"protein_coding","ncbi_id":"4722","summary":"This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.[provided by RefSeq, Apr 2009]","start":47565336,"end":47584562,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S3 [Source:HGNC Symbol;Acc:HGNC:7710]"}, {"versioned_ensembl_gene_id":"ENSG00000275416.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,cl-5,nkat4b,nkat4,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850500,"end":54867258,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000278206.1","gene_symbol":"AL031320.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143484979,"end":143507327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104863.11","gene_symbol":"LIN7B","gene_name":"lin-7 homolog B, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17788]","synonyms":"VELI2,MALS-2,LIN-7B","biotype":"protein_coding","ncbi_id":"64130","summary":null,"start":49114324,"end":49118460,"strand":1,"description":"lin-7 homolog B, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17788]"}, {"versioned_ensembl_gene_id":"ENSG00000110848.8","gene_symbol":"CD69","gene_name":"CD69 molecule [Source:HGNC Symbol;Acc:HGNC:1694]","synonyms":"CLEC2C","biotype":"protein_coding","ncbi_id":"969","summary":"This gene encodes a member of the calcium dependent lectin superfamily of type II transmembrane receptors. Expression of the encoded protein is induced upon activation of T lymphocytes, and may play a role in proliferation. Furthermore, the protein may act to transmit signals in natural killer cells and platelets. [provided by RefSeq, Aug 2011]","start":9752486,"end":9760901,"strand":-1,"description":"CD69 molecule [Source:HGNC Symbol;Acc:HGNC:1694]"}, {"versioned_ensembl_gene_id":"ENSG00000239544.1","gene_symbol":"AL442663.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72963645,"end":72964008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196843.15","gene_symbol":"ARID5A","gene_name":"AT-rich interaction domain 5A [Source:HGNC Symbol;Acc:HGNC:17361]","synonyms":"RP11-363D14,MRF-1","biotype":"protein_coding","ncbi_id":"10865","summary":"Members of the ARID protein family, including ARID5A, have diverse functions but all appear to play important roles in development, tissue-specific gene expression, and regulation of cell growth (Patsialou et al., 2005 [PubMed 15640446]).[supplied by OMIM, Mar 2008]","start":96536743,"end":96552638,"strand":1,"description":"AT-rich interaction domain 5A [Source:HGNC Symbol;Acc:HGNC:17361]"}, {"versioned_ensembl_gene_id":"ENSG00000104848.1","gene_symbol":"KCNA7","gene_name":"potassium voltage-gated channel subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:6226]","synonyms":"Kv1.7,HAK6","biotype":"protein_coding","ncbi_id":"3743","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. The gene is expressed preferentially in skeletal muscle, heart and kidney. It is a candidate gene for inherited cardiac disorders. [provided by RefSeq, Jul 2008]","start":49067418,"end":49072941,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:6226]"}, {"versioned_ensembl_gene_id":"ENSG00000225361.3","gene_symbol":"PPP1R26-AS1","gene_name":"PPP1R26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48717]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506599","summary":null,"start":135462727,"end":135480777,"strand":-1,"description":"PPP1R26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48717]"}, {"versioned_ensembl_gene_id":"ENSG00000120329.6","gene_symbol":"SLC25A2","gene_name":"solute carrier family 25 member 2 [Source:HGNC Symbol;Acc:HGNC:22921]","synonyms":"ORNT2","biotype":"protein_coding","ncbi_id":"83884","summary":"This intronless gene encodes a protein that localizes to the mitochondrial inner membrane and likely functions as a transporter of small molecules such as ornithine. This gene is located between the protocadherin beta and gamma gene clusters on chromosome 5. [provided by RefSeq, Dec 2014]","start":141302629,"end":141304045,"strand":-1,"description":"solute carrier family 25 member 2 [Source:HGNC Symbol;Acc:HGNC:22921]"}, {"versioned_ensembl_gene_id":"ENSG00000253923.2","gene_symbol":"AP002981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102417979,"end":102418953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273723.1","gene_symbol":"AL139089.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52651305,"end":52652279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239920.1","gene_symbol":"AC015691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5572322,"end":5624896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196422.10","gene_symbol":"PPP1R26","gene_name":"protein phosphatase 1 regulatory subunit 26 [Source:HGNC Symbol;Acc:HGNC:29089]","synonyms":"KIAA0649","biotype":"protein_coding","ncbi_id":"9858","summary":null,"start":135479079,"end":135488893,"strand":1,"description":"protein phosphatase 1 regulatory subunit 26 [Source:HGNC Symbol;Acc:HGNC:29089]"}, {"versioned_ensembl_gene_id":"ENSG00000240040.6","gene_symbol":"AC244205.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":88811186,"end":88861563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267334.1","gene_symbol":"AC015936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44947912,"end":44948939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259023.2","gene_symbol":"LINC00524","gene_name":"long intergenic non-protein coding RNA 524 [Source:HGNC Symbol;Acc:HGNC:20118]","synonyms":"C14orf71","biotype":"lincRNA","ncbi_id":"338002","summary":null,"start":101405987,"end":101407922,"strand":-1,"description":"long intergenic non-protein coding RNA 524 [Source:HGNC Symbol;Acc:HGNC:20118]"}, {"versioned_ensembl_gene_id":"ENSG00000142959.4","gene_symbol":"BEST4","gene_name":"bestrophin 4 [Source:HGNC Symbol;Acc:HGNC:17106]","synonyms":"VMD2L2","biotype":"protein_coding","ncbi_id":"266675","summary":"This gene is a member of the bestrophin gene family of anion channels. Bestrophin genes share a similar gene structure with highly conserved exon-intron boundaries, but with distinct 3' ends. Bestrophins are transmembrane proteins that contain a homologous region rich in aromatic residues, including an invariant arg-phe-pro motif. Mutation in one of the family members (bestrophin 1) is associated with vitelliform macular dystrophy. The bestrophin 4 gene is predominantly expressed in the colon. [provided by RefSeq, Jul 2008]","start":44783585,"end":44787705,"strand":-1,"description":"bestrophin 4 [Source:HGNC Symbol;Acc:HGNC:17106]"}, {"versioned_ensembl_gene_id":"ENSG00000223851.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30678268,"end":30678534,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000163812.13","gene_symbol":"ZDHHC3","gene_name":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]","synonyms":"ZNF373,GODZ,DHHC3","biotype":"protein_coding","ncbi_id":"51304","summary":null,"start":44915257,"end":44976185,"strand":-1,"description":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]"}, {"versioned_ensembl_gene_id":"ENSG00000170949.17","gene_symbol":"ZNF160","gene_name":"zinc finger protein 160 [Source:HGNC Symbol;Acc:HGNC:12948]","synonyms":"HKr18,FLJ00032,F11,KR18,KIAA1611,HZF5","biotype":"protein_coding","ncbi_id":"90338","summary":"The protein encoded by this gene is a Kruppel-related zinc finger protein which is characterized by the presence of an N-terminal repressor domain, the Kruppel-associated box (KRAB). The KRAB domain is a potent repressor of transcription; thus this protein may function in transcription regulation. Multiple transcript variants have been found for this gene. [provided by RefSeq, Apr 2016]","start":53066606,"end":53103436,"strand":-1,"description":"zinc finger protein 160 [Source:HGNC Symbol;Acc:HGNC:12948]"}, {"versioned_ensembl_gene_id":"ENSG00000229109.1","gene_symbol":"AL137847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83219331,"end":83234242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275718.1","gene_symbol":"CCL15","gene_name":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]","synonyms":"NCC-3,MIP-5,MIP-1d,Lkn-1,HMRP-2B,HCC-2,SCYL3,SCYA15","biotype":"protein_coding","ncbi_id":"6359","summary":"This gene is located in a cluster of similar genes in the same region of chromosome 17. These genes encode CC cytokines, which are secreted proteins characterized by two adjacent cysteines. The product of this gene is chemotactic for T cells and monocytes, and acts through C-C chemokine receptor type 1 (CCR1). The proprotein is further processed into numerous smaller functional peptides. Naturally-occurring readthrough transcripts occur from this gene into the downstream gene, CCL14 (chemokine (C-C motif) ligand 14). [provided by RefSeq, Jan 2013]","start":35996440,"end":36002038,"strand":-1,"description":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]"}, {"versioned_ensembl_gene_id":"ENSG00000273784.4","gene_symbol":"AL137058.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52600042,"end":52642542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120328.6","gene_symbol":"PCDHB12","gene_name":"protocadherin beta 12 [Source:HGNC Symbol;Acc:HGNC:8683]","synonyms":"PCDH-BETA12","biotype":"protein_coding","ncbi_id":"56124","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141208697,"end":141212571,"strand":1,"description":"protocadherin beta 12 [Source:HGNC Symbol;Acc:HGNC:8683]"}, {"versioned_ensembl_gene_id":"ENSG00000281708.1","gene_symbol":"ERC2-IT1","gene_name":"ERC2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1229]","synonyms":"C3orf51,C1orf1,Po42","biotype":"sense_intronic","ncbi_id":"711","summary":"This gene is a putative tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":55657206,"end":55659382,"strand":-1,"description":"ERC2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1229]"}, {"versioned_ensembl_gene_id":"ENSG00000113248.5","gene_symbol":"PCDHB15","gene_name":"protocadherin beta 15 [Source:HGNC Symbol;Acc:HGNC:8686]","synonyms":"PCDH-BETA15","biotype":"protein_coding","ncbi_id":"56121","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141245349,"end":141249365,"strand":1,"description":"protocadherin beta 15 [Source:HGNC Symbol;Acc:HGNC:8686]"}, {"versioned_ensembl_gene_id":"ENSG00000188488.13","gene_symbol":"SERPINA5","gene_name":"serpin family A member 5 [Source:HGNC Symbol;Acc:HGNC:8723]","synonyms":"PROCI,PLANH3,PCI,PAI3","biotype":"protein_coding","ncbi_id":"5104","summary":"The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. This family member is a glycoprotein that can inhibit several serine proteases, including protein C and various plasminogen activators and kallikreins, and it thus plays diverse roles in hemostasis and thrombosis in multiple organs. [provided by RefSeq, Aug 2012]","start":94561442,"end":94593120,"strand":1,"description":"serpin family A member 5 [Source:HGNC Symbol;Acc:HGNC:8723]"}, {"versioned_ensembl_gene_id":"ENSG00000236911.6","gene_symbol":"AL137789.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":207551925,"end":207606555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233342.1","gene_symbol":"AL391361.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160926369,"end":160927162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235984.5","gene_symbol":"GPC5-AS1","gene_name":"GPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39886]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873969","summary":null,"start":92701389,"end":92721614,"strand":-1,"description":"GPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39886]"}, {"versioned_ensembl_gene_id":"ENSG00000282865.1","gene_symbol":"AL157815.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92239835,"end":92241951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282993.1","gene_symbol":"AL356737.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92658994,"end":92659227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273259.3","gene_symbol":"AL049839.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":94592058,"end":94624646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229287.1","gene_symbol":"FABP5P4","gene_name":"fatty acid binding protein 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31061]","synonyms":"FABP5L4","biotype":"processed_pseudogene","ncbi_id":"404766","summary":null,"start":92180715,"end":92180885,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31061]"}, {"versioned_ensembl_gene_id":"ENSG00000231880.2","gene_symbol":"KF459542.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47577725,"end":47578277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008438.4","gene_symbol":"PGLYRP1","gene_name":"peptidoglycan recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:8904]","synonyms":"TNFSF3L,TAG7,PGRPS,PGRP-S,PGRP,PGLYRP","biotype":"protein_coding","ncbi_id":"8993","summary":null,"start":46019153,"end":46023065,"strand":-1,"description":"peptidoglycan recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:8904]"}, {"versioned_ensembl_gene_id":"ENSG00000113971.19","gene_symbol":"NPHP3","gene_name":"nephrocystin 3 [Source:HGNC Symbol;Acc:HGNC:7907]","synonyms":"CFAP31,SLSN3,NPH3,MKS7,KIAA2000,FLJ36696,FLJ30691","biotype":"protein_coding","ncbi_id":"27031","summary":"This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011]","start":132680609,"end":132722442,"strand":-1,"description":"nephrocystin 3 [Source:HGNC Symbol;Acc:HGNC:7907]"}, {"versioned_ensembl_gene_id":"ENSG00000275722.4","gene_symbol":"LYZL6","gene_name":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]","synonyms":"TKAL754,PRO1485,LYC1","biotype":"protein_coding","ncbi_id":"57151","summary":"This gene encodes a member of the C-type lysozyme/alpha-lactalbumin family. C-type lysozymes are bacteriolytic factors that play a role in host defense, whereas alpha-lactalbumins mediate lactose biosynthesis. The encoded protein contains catalytic residues characteristic of C-type lysozymes and may play a role in male reproduction. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2011]","start":35934518,"end":35943699,"strand":-1,"description":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]"}, {"versioned_ensembl_gene_id":"ENSG00000174373.16","gene_symbol":"RALGAPA1","gene_name":"Ral GTPase activating protein catalytic alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:17770]","synonyms":"Tulip1,RalGAPalpha1,KIAA0884,GRIPE,GARNL1,DKFZp667F074","biotype":"protein_coding","ncbi_id":"253959","summary":"This gene encodes a major subunit of the RAL-GTPase activating protein. A similar protein in mouse binds E12, a transcriptional regulator of immunoglobulin genes. The mouse protein also functions in skeletal muscle by binding to the regulatory 14-3-3 proteins upon stimulation with insulin or muscle contraction. A pseudogene of this gene has been identified on chromosome 9. [provided by RefSeq, Oct 2016]","start":35538352,"end":35809304,"strand":-1,"description":"Ral GTPase activating protein catalytic alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:17770]"}, {"versioned_ensembl_gene_id":"ENSG00000231562.1","gene_symbol":"AL512593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106978776,"end":106979554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260879.1","gene_symbol":"AL359258.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108199926,"end":108201491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044115.20","gene_symbol":"CTNNA1","gene_name":"catenin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2509]","synonyms":"CAP102","biotype":"protein_coding","ncbi_id":"1495","summary":"This gene encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin-actin filament connections. Certain mutations in this gene cause butterfly-shaped pigment dystrophy. [provided by RefSeq, May 2016]","start":138610967,"end":138935034,"strand":1,"description":"catenin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2509]"}, {"versioned_ensembl_gene_id":"ENSG00000236051.7","gene_symbol":"MYCBP2-AS1","gene_name":"MYCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41023]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874212","summary":null,"start":77026767,"end":77129717,"strand":1,"description":"MYCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41023]"}, {"versioned_ensembl_gene_id":"ENSG00000234474.2","gene_symbol":"MIR3663HG","gene_name":"MIR3663 host gene [Source:HGNC Symbol;Acc:HGNC:50676]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927704","summary":null,"start":117158656,"end":117169059,"strand":-1,"description":"MIR3663 host gene [Source:HGNC Symbol;Acc:HGNC:50676]"}, {"versioned_ensembl_gene_id":"ENSG00000225475.1","gene_symbol":"AC099789.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56619409,"end":56619549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271484.1","gene_symbol":"ABI1P1","gene_name":"abl interactor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20035]","synonyms":"SSH3BP1P,ABI1P","biotype":"unprocessed_pseudogene","ncbi_id":"326268","summary":null,"start":55546674,"end":55548123,"strand":1,"description":"abl interactor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20035]"}, {"versioned_ensembl_gene_id":"ENSG00000122194.18","gene_symbol":"PLG","gene_name":"plasminogen [Source:HGNC Symbol;Acc:HGNC:9071]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5340","summary":"The plasminogen protein encoded by this gene is a serine protease that circulates in blood plasma as an inactive zymogen and is converted to the active protease, plasmin, by several plasminogen activators such as tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, and factor XII (Hageman factor). The conversion of plasminogen to plasmin involves the cleavage of the peptide bond between Arg-561 and Val-562. Plasmin cleavage also releases the angiostatin protein which inhibits angiogenesis. Plasmin degrades many blood plasma proteins, including fibrin-containing blood clots. As a serine protease, plasmin cleaves many products in addition to fibrin such as fibronectin, thrombospondin, laminin, and von Willebrand factor. Plasmin is inactivated by proteins such as alpha-2-macroglobulin and alpha-2-antiplasmin in addition to inhibitors of the various plasminogen activators. Plasminogen also interacts with plasminogen receptors which results in the retention of plasmin on cell surfaces and in plasmin-induced cell signaling. The localization of plasminogen on cell surfaces plays a role in the degradation of extracellular matrices, cell migration, inflamation, wound healing, oncogenesis, metastasis, myogenesis, muscle regeneration, neurite outgrowth, and fibrinolysis. This protein may also play a role in acute respiratory distress syndrome (ARDS) which, in part, is caused by enhanced clot formation and the suppression of fibrinolysis. Compared to other mammals, the cluster of plasminogen-like genes to which this gene belongs has been rearranged in catarrhine primates. [provided by RefSeq, May 2020]","start":160702238,"end":160753315,"strand":1,"description":"plasminogen [Source:HGNC Symbol;Acc:HGNC:9071]"}, {"versioned_ensembl_gene_id":"ENSG00000233259.4","gene_symbol":"FABP3P2","gene_name":"fatty acid binding protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3558]","synonyms":"FABP3P,FABP3-ps","biotype":"processed_pseudogene","ncbi_id":"56677","summary":null,"start":42369259,"end":42369657,"strand":-1,"description":"fatty acid binding protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3558]"}, {"versioned_ensembl_gene_id":"ENSG00000112319.17","gene_symbol":"EYA4","gene_name":"EYA transcriptional coactivator and phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3522]","synonyms":"DFNA10,CMD1J","biotype":"protein_coding","ncbi_id":"2070","summary":"This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":133240598,"end":133532120,"strand":1,"description":"EYA transcriptional coactivator and phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3522]"}, {"versioned_ensembl_gene_id":"ENSG00000163864.15","gene_symbol":"NMNAT3","gene_name":"nicotinamide nucleotide adenylyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:20989]","synonyms":"PNAT3","biotype":"protein_coding","ncbi_id":"349565","summary":"This gene encodes a member of the nicotinamide/nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide, respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":139560180,"end":139678017,"strand":-1,"description":"nicotinamide nucleotide adenylyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:20989]"}, {"versioned_ensembl_gene_id":"ENSG00000224477.5","gene_symbol":"AL109933.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160698288,"end":160700632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090861.15","gene_symbol":"AARS","gene_name":"alanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:20]","synonyms":"CMT2N,AlaRS","biotype":"protein_coding","ncbi_id":"16","summary":"The human alanyl-tRNA synthetase (AARS) belongs to a family of tRNA synthases, of the class II enzymes. Class II tRNA synthases evolved early in evolution and are highly conserved. This is reflected by the fact that 498 of the 968-residue polypeptide human AARS shares 41% identity witht the E.coli protein. tRNA synthases are the enzymes that interpret the RNA code and attach specific aminoacids to the tRNAs that contain the cognate trinucleotide anticodons. They consist of a catalytic domain which interacts with the amino acid acceptor-T psi C helix of the tRNA, and a second domain which interacts with the rest of the tRNA structure. [provided by RefSeq, Jul 2008]","start":70252295,"end":70289543,"strand":-1,"description":"alanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:20]"}, {"versioned_ensembl_gene_id":"ENSG00000227954.6","gene_symbol":"TARID","gene_name":"TCF21 antisense RNA inducing promoter demethylation [Source:HGNC Symbol;Acc:HGNC:50506]","synonyms":"EYA4-AS1","biotype":"antisense_RNA","ncbi_id":"100507308","summary":null,"start":133502252,"end":133892802,"strand":-1,"description":"TCF21 antisense RNA inducing promoter demethylation [Source:HGNC Symbol;Acc:HGNC:50506]"}, {"versioned_ensembl_gene_id":"ENSG00000272428.1","gene_symbol":"AL450270.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133540784,"end":133541174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223586.5","gene_symbol":"LINC01312","gene_name":"long intergenic non-protein coding RNA 1312 [Source:HGNC Symbol;Acc:HGNC:28525]","synonyms":"MGC34034","biotype":"lincRNA","ncbi_id":"154089","summary":null,"start":133821147,"end":133851800,"strand":1,"description":"long intergenic non-protein coding RNA 1312 [Source:HGNC Symbol;Acc:HGNC:28525]"}, {"versioned_ensembl_gene_id":"ENSG00000226397.8","gene_symbol":"C12orf77","gene_name":"chromosome 12 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:27282]","synonyms":null,"biotype":"lincRNA","ncbi_id":"196415","summary":null,"start":24993424,"end":25006403,"strand":-1,"description":"chromosome 12 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:27282]"}, {"versioned_ensembl_gene_id":"ENSG00000263219.1","gene_symbol":"AC087742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4222091,"end":4223828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263165.1","gene_symbol":"AC087292.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4163910,"end":4164713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225205.5","gene_symbol":"AC078883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172480840,"end":172556596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279632.1","gene_symbol":"AP003108.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61426448,"end":61427325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256591.5","gene_symbol":"AP003108.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61429220,"end":61485822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189159.15","gene_symbol":"JPT1","gene_name":"Jupiter microtubule associated homolog 1 [Source:HGNC Symbol;Acc:HGNC:14569]","synonyms":"HN1A,HN1,ARM2","biotype":"protein_coding","ncbi_id":"51155","summary":null,"start":75135248,"end":75168281,"strand":-1,"description":"Jupiter microtubule associated homolog 1 [Source:HGNC Symbol;Acc:HGNC:14569]"}, {"versioned_ensembl_gene_id":"ENSG00000148660.20","gene_symbol":"CAMK2G","gene_name":"calcium/calmodulin dependent protein kinase II gamma [Source:HGNC Symbol;Acc:HGNC:1463]","synonyms":"CAMKG","biotype":"protein_coding","ncbi_id":"818","summary":"The product of this gene is one of the four subunits of an enzyme which belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a gamma chain. Many alternatively spliced transcripts encoding different isoforms have been described but the full-length nature of all the variants has not been determined.[provided by RefSeq, Mar 2011]","start":73812501,"end":73874591,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II gamma [Source:HGNC Symbol;Acc:HGNC:1463]"}, {"versioned_ensembl_gene_id":"ENSG00000261446.2","gene_symbol":"LINC00559","gene_name":"long intergenic non-protein coding RNA 559 [Source:HGNC Symbol;Acc:HGNC:43703]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874187","summary":null,"start":90060247,"end":90119719,"strand":-1,"description":"long intergenic non-protein coding RNA 559 [Source:HGNC Symbol;Acc:HGNC:43703]"}, {"versioned_ensembl_gene_id":"ENSG00000237566.1","gene_symbol":"AC090955.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5099627,"end":5099861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279456.1","gene_symbol":"AL353763.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41061290,"end":41062917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156508.17","gene_symbol":"EEF1A1","gene_name":"eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:3189]","synonyms":"EEF1A,EE1A1,LENG7,EF1A","biotype":"protein_coding","ncbi_id":"1915","summary":"This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expressed in brain, heart and skeletal muscle. This isoform is identified as an autoantigen in 66% of patients with Felty syndrome. This gene has been found to have multiple copies on many chromosomes, some of which, if not all, represent different pseudogenes. [provided by RefSeq, Jul 2008]","start":73515750,"end":73523797,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:3189]"}, {"versioned_ensembl_gene_id":"ENSG00000228970.6","gene_symbol":"UBTFL6","gene_name":"upstream binding transcription factor, RNA polymerase I-like 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35406]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643615","summary":null,"start":97636780,"end":97637803,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35406]"}, {"versioned_ensembl_gene_id":"ENSG00000186051.6","gene_symbol":"TAL2","gene_name":"TAL bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11557]","synonyms":"bHLHa19","biotype":"protein_coding","ncbi_id":"6887","summary":"This intronless gene encodes a helix-loop-helix protein. Translocations between this gene on chromosome 9 and the T-cell receptor beta-chain locus on chromosome 7 have been associated with activation of the T-cell acute lymphocytic leukemia 2 gene and T-cell acute lymphoblastic leukemia. [provided by RefSeq, Mar 2009]","start":105662457,"end":105663112,"strand":1,"description":"TAL bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11557]"}, {"versioned_ensembl_gene_id":"ENSG00000272629.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859613,"end":28863339,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000273122.1","gene_symbol":"AL844539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861404,"end":28862035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272473.1","gene_symbol":"AC006273.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":781002,"end":781862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227147.9","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30153123,"end":30162613,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000120526.10","gene_symbol":"NUDCD1","gene_name":"NudC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24306]","synonyms":"FLJ14991,CML66","biotype":"protein_coding","ncbi_id":"84955","summary":null,"start":109240919,"end":109334385,"strand":-1,"description":"NudC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24306]"}, {"versioned_ensembl_gene_id":"ENSG00000066827.15","gene_symbol":"ZFAT","gene_name":"zinc finger and AT-hook domain containing [Source:HGNC Symbol;Acc:HGNC:19899]","synonyms":"ZNF406,ZFAT1,KIAA1485","biotype":"protein_coding","ncbi_id":"57623","summary":"This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009]","start":134477788,"end":134713049,"strand":-1,"description":"zinc finger and AT-hook domain containing [Source:HGNC Symbol;Acc:HGNC:19899]"}, {"versioned_ensembl_gene_id":"ENSG00000248230.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29739210,"end":29746446,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000205940.8","gene_symbol":"HSP90AB2P","gene_name":"heat shock protein 90 alpha family class B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32537]","synonyms":"HSP90BB","biotype":"transcribed_processed_pseudogene","ncbi_id":"391634","summary":null,"start":13333414,"end":13338657,"strand":1,"description":"heat shock protein 90 alpha family class B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32537]"}, {"versioned_ensembl_gene_id":"ENSG00000111432.4","gene_symbol":"FZD10","gene_name":"frizzled class receptor 10 [Source:HGNC Symbol;Acc:HGNC:4039]","synonyms":"CD350","biotype":"protein_coding","ncbi_id":"11211","summary":"This gene is a member of the frizzled gene family. Members of this family encode 7-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. Using array analysis, expression of this intronless gene is significantly up-regulated in two cases of primary colon cancer. [provided by RefSeq, Jul 2008]","start":130162459,"end":130165740,"strand":1,"description":"frizzled class receptor 10 [Source:HGNC Symbol;Acc:HGNC:4039]"}, {"versioned_ensembl_gene_id":"ENSG00000139625.12","gene_symbol":"MAP3K12","gene_name":"mitogen-activated protein kinase kinase kinase 12 [Source:HGNC Symbol;Acc:HGNC:6851]","synonyms":"ZPKP1,ZPK,MUK,MEKK12,DLK","biotype":"protein_coding","ncbi_id":"7786","summary":"This gene encodes a member of the serine/threonine protein kinase family. This kinase contains a leucine-zipper domain and is predominately expressed in neuronal cells. The phosphorylation state of this kinase in synaptic terminals was shown to be regulated by membrane depolarization via calcineurin. This kinase forms heterodimers with leucine zipper containing transcription factors, such as cAMP responsive element binding protein (CREB) and MYC, and thus may play a regulatory role in PKA or retinoic acid induced neuronal differentiation. Alternatively spliced transcript variants encoding different proteins have been described.[provided by RefSeq, Jul 2010]","start":53479669,"end":53500063,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 12 [Source:HGNC Symbol;Acc:HGNC:6851]"}, {"versioned_ensembl_gene_id":"ENSG00000271180.1","gene_symbol":"AL158801.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55240622,"end":55241080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231937.1","gene_symbol":"AC116666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152138883,"end":152186857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258991.1","gene_symbol":"DUX4L19","gene_name":"double homeobox 4 like 19 [Source:HGNC Symbol;Acc:HGNC:37718]","synonyms":"DUXY4","biotype":"unprocessed_pseudogene","ncbi_id":"643034","summary":null,"start":11332329,"end":11333595,"strand":1,"description":"double homeobox 4 like 19 [Source:HGNC Symbol;Acc:HGNC:37718]"}, {"versioned_ensembl_gene_id":"ENSG00000248867.1","gene_symbol":"AC010625.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109448349,"end":109449063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168679.17","gene_symbol":"SLC16A4","gene_name":"solute carrier family 16 member 4 [Source:HGNC Symbol;Acc:HGNC:10925]","synonyms":"MCT5,MCT4","biotype":"protein_coding","ncbi_id":"9122","summary":null,"start":110362848,"end":110391082,"strand":-1,"description":"solute carrier family 16 member 4 [Source:HGNC Symbol;Acc:HGNC:10925]"}, {"versioned_ensembl_gene_id":"ENSG00000231649.3","gene_symbol":"SPATA31B1P","gene_name":"SPATA31 subfamily B member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:31411]","synonyms":"SPATA31B1,FAM75B,C9orf36B,bA388B24.2","biotype":"unprocessed_pseudogene","ncbi_id":"404770","summary":null,"start":82057647,"end":82063682,"strand":-1,"description":"SPATA31 subfamily B member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:31411]"}, {"versioned_ensembl_gene_id":"ENSG00000256906.1","gene_symbol":"LINC02419","gene_name":"long intergenic non-protein coding RNA 2419 [Source:HGNC Symbol;Acc:HGNC:53349]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370078","summary":null,"start":130070325,"end":130072685,"strand":1,"description":"long intergenic non-protein coding RNA 2419 [Source:HGNC Symbol;Acc:HGNC:53349]"}, {"versioned_ensembl_gene_id":"ENSG00000187164.19","gene_symbol":"SHTN1","gene_name":"shootin 1 [Source:HGNC Symbol;Acc:HGNC:29319]","synonyms":"shootin1,shootin-1,KIAA1598","biotype":"protein_coding","ncbi_id":"57698","summary":null,"start":116881482,"end":117126586,"strand":-1,"description":"shootin 1 [Source:HGNC Symbol;Acc:HGNC:29319]"}, {"versioned_ensembl_gene_id":"ENSG00000169641.13","gene_symbol":"LUZP1","gene_name":"leucine zipper protein 1 [Source:HGNC Symbol;Acc:HGNC:14985]","synonyms":"LUZP","biotype":"protein_coding","ncbi_id":"7798","summary":"This gene encodes a protein that contains a leucine zipper motif. The exact function of the encoded protein is not known. In mice this gene affects neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":23084023,"end":23177808,"strand":-1,"description":"leucine zipper protein 1 [Source:HGNC Symbol;Acc:HGNC:14985]"}, {"versioned_ensembl_gene_id":"ENSG00000276042.4","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"CD85k,LIR-5,ILT3,HM18,LIR5","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54592642,"end":54600251,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000266200.6","gene_symbol":"PNLIPRP2","gene_name":"pancreatic lipase related protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9157]","synonyms":"PLRP2","biotype":"polymorphic_pseudogene","ncbi_id":"5408","summary":"This gene encodes a lipase that hydrolyzes galactolipids, the main components of plant membrane lipids. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the non-coding allele. [provided by RefSeq, Aug 2015]","start":116620953,"end":116645143,"strand":1,"description":"pancreatic lipase related protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9157]"}, {"versioned_ensembl_gene_id":"ENSG00000168792.4","gene_symbol":"ABHD15","gene_name":"abhydrolase domain containing 15 [Source:HGNC Symbol;Acc:HGNC:26971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116236","summary":null,"start":29560547,"end":29567137,"strand":-1,"description":"abhydrolase domain containing 15 [Source:HGNC Symbol;Acc:HGNC:26971]"}, {"versioned_ensembl_gene_id":"ENSG00000184564.8","gene_symbol":"SLITRK6","gene_name":"SLIT and NTRK like family member 6 [Source:HGNC Symbol;Acc:HGNC:23503]","synonyms":"FLJ22774","biotype":"protein_coding","ncbi_id":"84189","summary":"This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]","start":85792790,"end":85799488,"strand":-1,"description":"SLIT and NTRK like family member 6 [Source:HGNC Symbol;Acc:HGNC:23503]"}, {"versioned_ensembl_gene_id":"ENSG00000259017.1","gene_symbol":"AL133163.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35447003,"end":35447625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266919.3","gene_symbol":"AC104984.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30117079,"end":30117172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154342.5","gene_symbol":"WNT3A","gene_name":"Wnt family member 3A [Source:HGNC Symbol;Acc:HGNC:15983]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89780","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 96% amino acid identity to mouse Wnt3A protein, and 84% to human WNT3 protein, another WNT gene product. This gene is clustered with WNT14 gene, another family member, in chromosome 1q42 region. [provided by RefSeq, Jul 2008]","start":228007051,"end":228061260,"strand":1,"description":"Wnt family member 3A [Source:HGNC Symbol;Acc:HGNC:15983]"}, {"versioned_ensembl_gene_id":"ENSG00000226317.2","gene_symbol":"LINC00351","gene_name":"long intergenic non-protein coding RNA 351 [Source:HGNC Symbol;Acc:HGNC:42669]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874137","summary":null,"start":85363601,"end":85544570,"strand":1,"description":"long intergenic non-protein coding RNA 351 [Source:HGNC Symbol;Acc:HGNC:42669]"}, {"versioned_ensembl_gene_id":"ENSG00000271490.1","gene_symbol":"AC013244.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50806335,"end":50806437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167720.12","gene_symbol":"SRR","gene_name":"serine racemase [Source:HGNC Symbol;Acc:HGNC:14398]","synonyms":"ISO1,ILV1","biotype":"protein_coding","ncbi_id":"63826","summary":null,"start":2303383,"end":2325260,"strand":1,"description":"serine racemase [Source:HGNC Symbol;Acc:HGNC:14398]"}, {"versioned_ensembl_gene_id":"ENSG00000232907.7","gene_symbol":"DLGAP4-AS1","gene_name":"DLGAP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51223]","synonyms":"CCAT7","biotype":"antisense_RNA","ncbi_id":"101926987","summary":null,"start":36507702,"end":36573391,"strand":-1,"description":"DLGAP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51223]"}, {"versioned_ensembl_gene_id":"ENSG00000244245.1","gene_symbol":"AC133134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108593609,"end":108593967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186268.3","gene_symbol":"OR10D4P","gene_name":"olfactory receptor family 10 subfamily D member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14770]","synonyms":"OR10D6P,OR10D4","biotype":"unprocessed_pseudogene","ncbi_id":"390266","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124093582,"end":124094532,"strand":-1,"description":"olfactory receptor family 10 subfamily D member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14770]"}, {"versioned_ensembl_gene_id":"ENSG00000182634.8","gene_symbol":"OR10G7","gene_name":"olfactory receptor family 10 subfamily G member 7 [Source:HGNC Symbol;Acc:HGNC:14842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390265","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124036013,"end":124041325,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 7 [Source:HGNC Symbol;Acc:HGNC:14842]"}, {"versioned_ensembl_gene_id":"ENSG00000103404.14","gene_symbol":"USP31","gene_name":"ubiquitin specific peptidase 31 [Source:HGNC Symbol;Acc:HGNC:20060]","synonyms":"KIAA1203","biotype":"protein_coding","ncbi_id":"57478","summary":null,"start":23061406,"end":23149270,"strand":-1,"description":"ubiquitin specific peptidase 31 [Source:HGNC Symbol;Acc:HGNC:20060]"}, {"versioned_ensembl_gene_id":"ENSG00000280400.1","gene_symbol":"AC127459.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23061767,"end":23062232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182979.17","gene_symbol":"MTA1","gene_name":"metastasis associated 1 [Source:HGNC Symbol;Acc:HGNC:7410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9112","summary":"This gene encodes a protein that was identified in a screen for genes expressed in metastatic cells, specifically, mammary adenocarcinoma cell lines. Expression of this gene has been correlated with the metastatic potential of at least two types of carcinomas although it is also expressed in many normal tissues. The role it plays in metastasis is unclear. It was initially thought to be the 70kD component of a nucleosome remodeling deacetylase complex, NuRD, but it is more likely that this component is a different but very similar protein. These two proteins are so closely related, though, that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. The profile and activity of this gene product suggest that it is involved in regulating transcription and that this may be accomplished by chromatin remodeling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":105419820,"end":105470729,"strand":1,"description":"metastasis associated 1 [Source:HGNC Symbol;Acc:HGNC:7410]"}, {"versioned_ensembl_gene_id":"ENSG00000185198.11","gene_symbol":"PRSS57","gene_name":"protease, serine 57 [Source:HGNC Symbol;Acc:HGNC:31397]","synonyms":"PRSSL1,UNQ782","biotype":"protein_coding","ncbi_id":"400668","summary":"This gene encodes an arginine-specific serine protease and member of the peptidase S1 family of proteins. The encoded protein may undergo proteolytic activation before storage in azurophil granules, in neutrophil cells of the immune system. Following neutrophil activation, the protease is released into the pericellular environment, where it may play a role in defense against microbial pathogens. [provided by RefSeq, Jul 2016]","start":685546,"end":695498,"strand":-1,"description":"protease, serine 57 [Source:HGNC Symbol;Acc:HGNC:31397]"}, {"versioned_ensembl_gene_id":"ENSG00000122254.6","gene_symbol":"HS3ST2","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:5195]","synonyms":"3OST2","biotype":"protein_coding","ncbi_id":"9956","summary":"Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. The enzyme encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. It is a type II integral membrane protein and possesses heparan sulfate glucosaminyl 3-O-sulfotransferase activity. This gene is expressed predominantly in brain and may play a role in the nervous system. [provided by RefSeq, Jul 2008]","start":22814177,"end":22916338,"strand":1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:5195]"}, {"versioned_ensembl_gene_id":"ENSG00000103769.9","gene_symbol":"RAB11A","gene_name":"RAB11A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9760]","synonyms":"YL8","biotype":"protein_coding","ncbi_id":"8766","summary":"The protein encoded by this gene belongs to the Rab family of the small GTPase superfamily. It is associated with both constitutive and regulated secretory pathways, and may be involved in protein transport. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":65726054,"end":65891991,"strand":1,"description":"RAB11A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9760]"}, {"versioned_ensembl_gene_id":"ENSG00000184349.12","gene_symbol":"EFNA5","gene_name":"ephrin A5 [Source:HGNC Symbol;Acc:HGNC:3225]","synonyms":"LERK7,EPLG7,AF1","biotype":"protein_coding","ncbi_id":"1946","summary":"Ephrin-A5, a member of the ephrin gene family, prevents axon bundling in cocultures of cortical neurons with astrocytes, a model of late stage nervous system development and differentiation. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. EPH receptors typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin ligands and receptors have been named by the Eph Nomenclature Committee (1997). Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are similarly divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. [provided by RefSeq, Jul 2008]","start":107376889,"end":107670895,"strand":-1,"description":"ephrin A5 [Source:HGNC Symbol;Acc:HGNC:3225]"}, {"versioned_ensembl_gene_id":"ENSG00000096696.13","gene_symbol":"DSP","gene_name":"desmoplakin [Source:HGNC Symbol;Acc:HGNC:3052]","synonyms":"PPKS2,KPPS2,DPII,DPI","biotype":"protein_coding","ncbi_id":"1832","summary":"This gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas, including skin fragility-woolly hair syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":7541575,"end":7586717,"strand":1,"description":"desmoplakin [Source:HGNC Symbol;Acc:HGNC:3052]"}, {"versioned_ensembl_gene_id":"ENSG00000120705.12","gene_symbol":"ETF1","gene_name":"eukaryotic translation termination factor 1 [Source:HGNC Symbol;Acc:HGNC:3477]","synonyms":"SUP45L1,RF1,ERF1,ERF,TB3-1","biotype":"protein_coding","ncbi_id":"2107","summary":"This gene encodes a class-1 polypeptide chain release factor. The encoded protein plays an essential role in directing termination of mRNA translation from the termination codons UAA, UAG and UGA. This protein is a component of the SURF complex which promotes degradation of prematurely terminated mRNAs via the mechanism of nonsense-mediated mRNA decay (NMD). Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 6, 7, and X. [provided by RefSeq, Aug 2013]","start":138506095,"end":138543300,"strand":-1,"description":"eukaryotic translation termination factor 1 [Source:HGNC Symbol;Acc:HGNC:3477]"}, {"versioned_ensembl_gene_id":"ENSG00000250364.6","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29374013,"end":29450575,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000102287.18","gene_symbol":"GABRE","gene_name":"gamma-aminobutyric acid type A receptor epsilon subunit [Source:HGNC Symbol;Acc:HGNC:4085]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2564","summary":"The product of this gene belongs to the ligand-gated ionic channel (TC 1.A.9) family. It encodes the gamma-aminobutyric acid (GABA) A receptor which is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes an epsilon subunit. It is mapped to chromosome Xq28 in a cluster comprised of genes encoding alpha 3, beta 4 and theta subunits of the same receptor. Alternatively spliced transcript variants have been identified, but only one is thought to encode a protein. [provided by RefSeq, Oct 2008]","start":151953124,"end":151974680,"strand":-1,"description":"gamma-aminobutyric acid type A receptor epsilon subunit [Source:HGNC Symbol;Acc:HGNC:4085]"}, {"versioned_ensembl_gene_id":"ENSG00000103024.7","gene_symbol":"NME3","gene_name":"NME/NM23 nucleoside diphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:7851]","synonyms":"NM23-H3,NDPKC,DR-nm23","biotype":"protein_coding","ncbi_id":"4832","summary":null,"start":1770286,"end":1771730,"strand":-1,"description":"NME/NM23 nucleoside diphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:7851]"}, {"versioned_ensembl_gene_id":"ENSG00000258417.3","gene_symbol":"AC100868.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":132024238,"end":132085655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116039.11","gene_symbol":"ATP6V1B1","gene_name":"ATPase H+ transporting V1 subunit B1 [Source:HGNC Symbol;Acc:HGNC:853]","synonyms":"ATP6B1,VPP3,Vma2,VATB,RTA1B","biotype":"protein_coding","ncbi_id":"525","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. [provided by RefSeq, Jul 2008]","start":70935882,"end":70965406,"strand":1,"description":"ATPase H+ transporting V1 subunit B1 [Source:HGNC Symbol;Acc:HGNC:853]"}, {"versioned_ensembl_gene_id":"ENSG00000224538.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29901898,"end":29902760,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000237072.1","gene_symbol":"AL161727.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81488308,"end":81488837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272735.1","gene_symbol":"AC007881.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71067519,"end":71068125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180616.8","gene_symbol":"SSTR2","gene_name":"somatostatin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11331]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6752","summary":"Somatostatin acts at many sites to inhibit the release of many hormones and other secretory proteins. The biologic effects of somatostatin are probably mediated by a family of G protein-coupled receptors that are expressed in a tissue-specific manner. SSTR2 is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in cerebrum and kidney. [provided by RefSeq, Jul 2008]","start":73165012,"end":73176633,"strand":1,"description":"somatostatin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11331]"}, {"versioned_ensembl_gene_id":"ENSG00000282407.1","gene_symbol":"AC229888.6","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142577660,"end":142578143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125503.12","gene_symbol":"PPP1R12C","gene_name":"protein phosphatase 1 regulatory subunit 12C [Source:HGNC Symbol;Acc:HGNC:14947]","synonyms":"p85,p84,MBS85,LENG3,DKFZP434D0412","biotype":"protein_coding","ncbi_id":"54776","summary":"The gene encodes a subunit of myosin phosphatase. The encoded protein regulates the catalytic activity of protein phosphatase 1 delta and assembly of the actin cytoskeleton. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":55090913,"end":55117559,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 12C [Source:HGNC Symbol;Acc:HGNC:14947]"}, {"versioned_ensembl_gene_id":"ENSG00000266501.1","gene_symbol":"AC025198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73067870,"end":73068288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230359.5","gene_symbol":"TPI1P2","gene_name":"triosephosphate isomerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38069]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"286016","summary":null,"start":129055223,"end":129057239,"strand":1,"description":"triosephosphate isomerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38069]"}, {"versioned_ensembl_gene_id":"ENSG00000154265.15","gene_symbol":"ABCA5","gene_name":"ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]","synonyms":"EST90625","biotype":"protein_coding","ncbi_id":"23461","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":69244311,"end":69327244,"strand":-1,"description":"ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]"}, {"versioned_ensembl_gene_id":"ENSG00000248853.1","gene_symbol":"AC113352.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121059244,"end":121060953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239552.2","gene_symbol":"HOXB-AS2","gene_name":"HOXB cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40284]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874350","summary":null,"start":48557262,"end":48560333,"strand":1,"description":"HOXB cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40284]"}, {"versioned_ensembl_gene_id":"ENSG00000248394.1","gene_symbol":"FOSL1P1","gene_name":"FOS like 1, AP-1 transcription factor subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419062","summary":null,"start":128155389,"end":128156204,"strand":1,"description":"FOS like 1, AP-1 transcription factor subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44055]"}, {"versioned_ensembl_gene_id":"ENSG00000103429.10","gene_symbol":"BFAR","gene_name":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]","synonyms":"RNF47,BAR","biotype":"protein_coding","ncbi_id":"51283","summary":null,"start":14632815,"end":14669236,"strand":1,"description":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]"}, {"versioned_ensembl_gene_id":"ENSG00000240934.2","gene_symbol":"AC066616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58200606,"end":58201018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259293.1","gene_symbol":"LIPC-AS1","gene_name":"LIPC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52294]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928694","summary":null,"start":58434890,"end":58498735,"strand":-1,"description":"LIPC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52294]"}, {"versioned_ensembl_gene_id":"ENSG00000280461.1","gene_symbol":"ABCB10P1","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]","synonyms":"ABCB10P2,ABCB10P,MABC2,M-ABC2","biotype":"processed_pseudogene","ncbi_id":"56476","summary":null,"start":23183337,"end":23185517,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]"}, {"versioned_ensembl_gene_id":"ENSG00000259626.2","gene_symbol":"MTND3P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075160","summary":null,"start":58150635,"end":58150962,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52072]"}, {"versioned_ensembl_gene_id":"ENSG00000132305.20","gene_symbol":"IMMT","gene_name":"inner membrane mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:6047]","synonyms":"P89,P87,MINOS2,Mic60,HMP","biotype":"protein_coding","ncbi_id":"10989","summary":null,"start":86143932,"end":86195770,"strand":-1,"description":"inner membrane mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:6047]"}, {"versioned_ensembl_gene_id":"ENSG00000278616.1","gene_symbol":"BEND3P3","gene_name":"BEN domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"650623","summary":null,"start":79682997,"end":79685436,"strand":1,"description":"BEN domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45016]"}, {"versioned_ensembl_gene_id":"ENSG00000272489.1","gene_symbol":"AL132656.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79663192,"end":79664786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282704.1","gene_symbol":"TRBV7-6","gene_name":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]","synonyms":"TRBV76,TCRBV7S6,TCRBV6S3A1N1T","biotype":"TR_V_gene","ncbi_id":"28592","summary":null,"start":142513848,"end":142514385,"strand":1,"description":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]"}, {"versioned_ensembl_gene_id":"ENSG00000213863.2","gene_symbol":"AL731661.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170725197,"end":170728488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232548.1","gene_symbol":"LINC01809","gene_name":"long intergenic non-protein coding RNA 1809 [Source:HGNC Symbol;Acc:HGNC:52612]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928031","summary":null,"start":83522814,"end":83523502,"strand":1,"description":"long intergenic non-protein coding RNA 1809 [Source:HGNC Symbol;Acc:HGNC:52612]"}, {"versioned_ensembl_gene_id":"ENSG00000236762.1","gene_symbol":"RPL19P16","gene_name":"ribosomal protein L19 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646255","summary":null,"start":121133090,"end":121133723,"strand":-1,"description":"ribosomal protein L19 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36596]"}, {"versioned_ensembl_gene_id":"ENSG00000259600.2","gene_symbol":"AC066616.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58151033,"end":58152513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207101.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41803349,"end":41803450,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000099250.17","gene_symbol":"NRP1","gene_name":"neuropilin 1 [Source:HGNC Symbol;Acc:HGNC:8004]","synonyms":"VEGF165R,NRP,CD304","biotype":"protein_coding","ncbi_id":"8829","summary":"This gene encodes one of two neuropilins, which contain specific protein domains which allow them to participate in several different types of signaling pathways that control cell migration. Neuropilins contain a large N-terminal extracellular domain, made up of complement-binding, coagulation factor V/VIII, and meprin domains. These proteins also contains a short membrane-spanning domain and a small cytoplasmic domain. Neuropilins bind many ligands and various types of co-receptors; they affect cell survival, migration, and attraction. Some of the ligands and co-receptors bound by neuropilins are vascular endothelial growth factor (VEGF) and semaphorin family members. This protein has also been determined to act as a co-receptor for SARS-CoV-2 (which causes COVID-19) to infect host cells. [provided by RefSeq, Nov 2020]","start":33177492,"end":33336262,"strand":-1,"description":"neuropilin 1 [Source:HGNC Symbol;Acc:HGNC:8004]"}, {"versioned_ensembl_gene_id":"ENSG00000117407.16","gene_symbol":"ARTN","gene_name":"artemin [Source:HGNC Symbol;Acc:HGNC:727]","synonyms":"NBN,EVN,ENOVIN","biotype":"protein_coding","ncbi_id":"9048","summary":"This gene encodes a secreted ligand of the glial cell line-derived neurotrophic factor (GDNF) subfamily and TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein signals through the RET receptor and GFR alpha 3 coreceptor, and supports the survival of a number of peripheral neuron populations and at least one population of dopaminergic CNS neurons. This protein has also been shown to promote tumor growth, metastasis, and drug resistance in mammary carcinoma. [provided by RefSeq, Aug 2016]","start":43933320,"end":43937241,"strand":1,"description":"artemin [Source:HGNC Symbol;Acc:HGNC:727]"}, {"versioned_ensembl_gene_id":"ENSG00000238002.2","gene_symbol":"NPAP1P6","gene_name":"nuclear pore associated protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533675","summary":null,"start":79863019,"end":79866875,"strand":1,"description":"nuclear pore associated protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45023]"}, {"versioned_ensembl_gene_id":"ENSG00000061337.15","gene_symbol":"LZTS1","gene_name":"leucine zipper tumor suppressor 1 [Source:HGNC Symbol;Acc:HGNC:13861]","synonyms":"FEZ1","biotype":"protein_coding","ncbi_id":"11178","summary":"This gene encodes a tumor suppressor protein that is ubiquitously expressed in normal tissues. In uveal melanomas, expression of this protein is silenced in rapidly metastasizing and metastatic tumor cells but has normal expression in slowly metastasizing or nonmetastasizing tumor cells. This protein may have a role in cell-cycle control by interacting with the Cdk1/cyclinB1 complex. This gene is located on chromosomal region 8p22. Loss of heterozygosity (LOH) in the 8p arm is a common characteristic of many types of cancer. [provided by RefSeq, Nov 2009]","start":20246165,"end":20303963,"strand":-1,"description":"leucine zipper tumor suppressor 1 [Source:HGNC Symbol;Acc:HGNC:13861]"}, {"versioned_ensembl_gene_id":"ENSG00000185982.6","gene_symbol":"DEFB128","gene_name":"defensin beta 128 [Source:HGNC Symbol;Acc:HGNC:18106]","synonyms":"DEFB-28","biotype":"protein_coding","ncbi_id":"245939","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":187853,"end":189681,"strand":-1,"description":"defensin beta 128 [Source:HGNC Symbol;Acc:HGNC:18106]"}, {"versioned_ensembl_gene_id":"ENSG00000260163.1","gene_symbol":"AC012508.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127025211,"end":127029686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173369.15","gene_symbol":"C1QB","gene_name":"complement C1q B chain [Source:HGNC Symbol;Acc:HGNC:1242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"713","summary":"This gene encodes the B-chain polypeptide of serum complement subcomponent C1q, which associates with C1r and C1s to yield the first component of the serum complement system. C1q is composed of 18 polypeptide chains which include 6 A-chains, 6 B-chains, and 6 C-chains. Each chain contains an N-terminal collagen-like region and a C-terminal C1q globular domain. C1q deficiency is associated with lupus erythematosus and glomerulonephritis. [provided by RefSeq, Dec 2016]","start":22652762,"end":22661538,"strand":1,"description":"complement C1q B chain [Source:HGNC Symbol;Acc:HGNC:1242]"}, {"versioned_ensembl_gene_id":"ENSG00000229011.1","gene_symbol":"LINC01038","gene_name":"long intergenic non-protein coding RNA 1038 [Source:HGNC Symbol;Acc:HGNC:49026]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724076","summary":null,"start":79804418,"end":79805685,"strand":1,"description":"long intergenic non-protein coding RNA 1038 [Source:HGNC Symbol;Acc:HGNC:49026]"}, {"versioned_ensembl_gene_id":"ENSG00000076053.10","gene_symbol":"RBM7","gene_name":"RNA binding motif protein 7 [Source:HGNC Symbol;Acc:HGNC:9904]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10179","summary":null,"start":114400030,"end":114414203,"strand":1,"description":"RNA binding motif protein 7 [Source:HGNC Symbol;Acc:HGNC:9904]"}, {"versioned_ensembl_gene_id":"ENSG00000159322.17","gene_symbol":"ADPGK","gene_name":"ADP dependent glucokinase [Source:HGNC Symbol;Acc:HGNC:25250]","synonyms":"DKFZp434B195,ADP-GK","biotype":"protein_coding","ncbi_id":"83440","summary":"ADPGK (EC 2.7.1.147) catalyzes the ADP-dependent phosphorylation of glucose to glucose-6-phosphate and may play a role in glycolysis, possibly during ischemic conditions (Ronimus and Morgan, 2004 [PubMed 14975750]).[supplied by OMIM, Mar 2008]","start":72751369,"end":72785846,"strand":-1,"description":"ADP dependent glucokinase [Source:HGNC Symbol;Acc:HGNC:25250]"}, {"versioned_ensembl_gene_id":"ENSG00000129991.12","gene_symbol":"TNNI3","gene_name":"troponin I3, cardiac type [Source:HGNC Symbol;Acc:HGNC:11947]","synonyms":"TNNC1,CMH7,CMD2A","biotype":"protein_coding","ncbi_id":"7137","summary":"Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). Troponin I is useful in making a diagnosis of heart failure, and of ischemic heart disease. An elevated level of troponin is also now used as indicator of acute myocardial injury in patients hospitalized with moderate/severe Coronavirus Disease 2019 (COVID-19). Such elevation has also been associated with higher risk of mortality in cardiovascular disease patients hospitalized due to COVID-19. [provided by RefSeq, Aug 2020]","start":55151767,"end":55157773,"strand":-1,"description":"troponin I3, cardiac type [Source:HGNC Symbol;Acc:HGNC:11947]"}, {"versioned_ensembl_gene_id":"ENSG00000171446.6","gene_symbol":"KRT27","gene_name":"keratin 27 [Source:HGNC Symbol;Acc:HGNC:30841]","synonyms":"KRT25C","biotype":"protein_coding","ncbi_id":"342574","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40776808,"end":40782534,"strand":-1,"description":"keratin 27 [Source:HGNC Symbol;Acc:HGNC:30841]"}, {"versioned_ensembl_gene_id":"ENSG00000214857.4","gene_symbol":"SEM1P1","gene_name":"SEM1, 26S proteasome complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24454]","synonyms":"SHFM1P1,SHFM1P,DSS1P1","biotype":"processed_pseudogene","ncbi_id":"153842","summary":null,"start":81892490,"end":81892721,"strand":1,"description":"SEM1, 26S proteasome complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24454]"}, {"versioned_ensembl_gene_id":"ENSG00000274695.1","gene_symbol":"AC108704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128826836,"end":128827579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201420.1","gene_symbol":"RNA5SP512","gene_name":"RNA, 5S ribosomal pseudogene 512 [Source:HGNC Symbol;Acc:HGNC:43412]","synonyms":"RN5S512","biotype":"rRNA","ncbi_id":"100873563","summary":null,"start":111669829,"end":111669948,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 512 [Source:HGNC Symbol;Acc:HGNC:43412]"}, {"versioned_ensembl_gene_id":"ENSG00000249743.5","gene_symbol":"AC116345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73213947,"end":73294934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136942.14","gene_symbol":"RPL35","gene_name":"ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:10344]","synonyms":"L35","biotype":"protein_coding","ncbi_id":"11224","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L29P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":124857880,"end":124861981,"strand":-1,"description":"ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:10344]"}, {"versioned_ensembl_gene_id":"ENSG00000109906.13","gene_symbol":"ZBTB16","gene_name":"zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:12930]","synonyms":"ZNF145,PLZF","biotype":"protein_coding","ncbi_id":"7704","summary":"This gene is a member of the Krueppel C2H2-type zinc-finger protein family and encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the carboxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, and interacts with a histone deacetylase. Specific instances of aberrant gene rearrangement at this locus have been associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":114059593,"end":114250676,"strand":1,"description":"zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:12930]"}, {"versioned_ensembl_gene_id":"ENSG00000070808.15","gene_symbol":"CAMK2A","gene_name":"calcium/calmodulin dependent protein kinase II alpha [Source:HGNC Symbol;Acc:HGNC:1460]","synonyms":"KIAA0968,CaMKIINalpha,CAMKA","biotype":"protein_coding","ncbi_id":"815","summary":"The product of this gene belongs to the serine/threonine protein kinases family, and to the Ca(2+)/calmodulin-dependent protein kinases subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. This calcium calmodulin-dependent protein kinase is composed of four different chains: alpha, beta, gamma, and delta. The alpha chain encoded by this gene is required for hippocampal long-term potentiation (LTP) and spatial learning. In addition to its calcium-calmodulin (CaM)-dependent activity, this protein can undergo autophosphorylation, resulting in CaM-independent activity. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2018]","start":150219491,"end":150290291,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II alpha [Source:HGNC Symbol;Acc:HGNC:1460]"}, {"versioned_ensembl_gene_id":"ENSG00000237300.2","gene_symbol":"MTCO1P19","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075144","summary":null,"start":102796251,"end":102797093,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52021]"}, {"versioned_ensembl_gene_id":"ENSG00000030419.16","gene_symbol":"IKZF2","gene_name":"IKAROS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13177]","synonyms":"ZNFN1A2,Helios","biotype":"protein_coding","ncbi_id":"22807","summary":"This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":212999691,"end":213152427,"strand":-1,"description":"IKAROS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13177]"}, {"versioned_ensembl_gene_id":"ENSG00000234429.1","gene_symbol":"AC105342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81194337,"end":81201184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234424.2","gene_symbol":"AL353743.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85753306,"end":85786575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261751.1","gene_symbol":"AC007603.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49920730,"end":49924154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148200.16","gene_symbol":"NR6A1","gene_name":"nuclear receptor subfamily 6 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7985]","synonyms":"CT150,RTR,GCNF1,GCNF","biotype":"protein_coding","ncbi_id":"2649","summary":"This gene encodes an orphan nuclear receptor which is a member of the nuclear hormone receptor family. Its expression pattern suggests that it may be involved in neurogenesis and germ cell development. The protein can homodimerize and bind DNA, but in vivo targets have not been identified. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jun 2013]","start":124517275,"end":124771310,"strand":-1,"description":"nuclear receptor subfamily 6 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7985]"}, {"versioned_ensembl_gene_id":"ENSG00000117360.12","gene_symbol":"PRPF3","gene_name":"pre-mRNA processing factor 3 [Source:HGNC Symbol;Acc:HGNC:17348]","synonyms":"SNRNP90,RP18,Prp3,hPrp3","biotype":"protein_coding","ncbi_id":"9129","summary":"The removal of introns from nuclear pre-mRNAs occurs on complexes called spliceosomes, which are made up of 4 small nuclear ribonucleoprotein (snRNP) particles and an undefined number of transiently associated splicing factors. This gene product is one of several proteins that associate with U4 and U6 snRNPs. Mutations in this gene are associated with retinitis pigmentosa-18. [provided by RefSeq, Jul 2008]","start":150321476,"end":150353195,"strand":1,"description":"pre-mRNA processing factor 3 [Source:HGNC Symbol;Acc:HGNC:17348]"}, {"versioned_ensembl_gene_id":"ENSG00000147655.10","gene_symbol":"RSPO2","gene_name":"R-spondin 2 [Source:HGNC Symbol;Acc:HGNC:28583]","synonyms":"MGC35555","biotype":"protein_coding","ncbi_id":"340419","summary":"This gene encodes a member of the R-spondin family of proteins. These proteins are secreted ligands of leucine-rich repeat containing G protein-coupled receptors that enhance Wnt signaling through the inhibition of ubiquitin E3 ligases. A chromosomal translocation including this locus that results in the formation of a gene fusion has been identified in multiple human cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":107899316,"end":108083648,"strand":-1,"description":"R-spondin 2 [Source:HGNC Symbol;Acc:HGNC:28583]"}, {"versioned_ensembl_gene_id":"ENSG00000165494.11","gene_symbol":"PCF11","gene_name":"PCF11 cleavage and polyadenylation factor subunit [Source:HGNC Symbol;Acc:HGNC:30097]","synonyms":"KIAA0824","biotype":"protein_coding","ncbi_id":"51585","summary":"The protein encoded by this gene binds to CLP1 to form pre-mRNA cleavage factor IIm. The encoded protein is necessary for efficient Pol II transcription termination and may be involved in degradation of the 3' product of polyA site cleavage. [provided by RefSeq, Oct 2016]","start":83156988,"end":83187451,"strand":1,"description":"PCF11 cleavage and polyadenylation factor subunit [Source:HGNC Symbol;Acc:HGNC:30097]"}, {"versioned_ensembl_gene_id":"ENSG00000251639.2","gene_symbol":"AC092535.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1100016,"end":1101558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274780.2","gene_symbol":"PHRF1","gene_name":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]","synonyms":"PPP1R125,KIAA1542,RNF221","biotype":"protein_coding","ncbi_id":"57661","summary":null,"start":576501,"end":612474,"strand":1,"description":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]"}, {"versioned_ensembl_gene_id":"ENSG00000273243.1","gene_symbol":"Z82243.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45155539,"end":45156011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177045.7","gene_symbol":"SIX5","gene_name":"SIX homeobox 5 [Source:HGNC Symbol;Acc:HGNC:10891]","synonyms":"DMAHP","biotype":"protein_coding","ncbi_id":"147912","summary":"The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2. [provided by RefSeq, Jul 2009]","start":45764785,"end":45769226,"strand":-1,"description":"SIX homeobox 5 [Source:HGNC Symbol;Acc:HGNC:10891]"}, {"versioned_ensembl_gene_id":"ENSG00000201161.1","gene_symbol":"RN7SKP10","gene_name":"RNA, 7SK small nuclear pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42628]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873873","summary":null,"start":109915096,"end":109915420,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42628]"}, {"versioned_ensembl_gene_id":"ENSG00000263468.1","gene_symbol":"hsa-mir-3130-1","gene_name":"hsa-mir-3130-1 [Source:miRBase;Acc:MI0014147]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":206783234,"end":206783308,"strand":1,"description":"hsa-mir-3130-1 [Source:miRBase;Acc:MI0014147]"}, {"versioned_ensembl_gene_id":"ENSG00000261879.5","gene_symbol":"AC087500.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5192084,"end":5248069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263164.1","gene_symbol":"AC087500.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5240508,"end":5241543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089737.16","gene_symbol":"DDX24","gene_name":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57062","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which shows little similarity to any of the other known human DEAD box proteins, but shows a high similarity to mouse Ddx24 at the amino acid level. [provided by RefSeq, Jul 2008]","start":94048291,"end":94081245,"strand":-1,"description":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]"}, {"versioned_ensembl_gene_id":"ENSG00000226328.6","gene_symbol":"NUP50-AS1","gene_name":"NUP50 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506714","summary":null,"start":45133020,"end":45163781,"strand":-1,"description":"NUP50 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50502]"}, {"versioned_ensembl_gene_id":"ENSG00000130822.15","gene_symbol":"PNCK","gene_name":"pregnancy up-regulated nonubiquitous CaM kinase [Source:HGNC Symbol;Acc:HGNC:13415]","synonyms":"MGC45419,CaMK1b","biotype":"protein_coding","ncbi_id":"139728","summary":"PNCK is a member of the calcium/calmodulin-dependent protein kinase family of protein serine/threonine kinases (see CAMK1; MIM 604998) (Gardner et al., 2000 [PubMed 10673339]).[supplied by OMIM, Mar 2008]","start":153669730,"end":153689010,"strand":-1,"description":"pregnancy up-regulated nonubiquitous CaM kinase [Source:HGNC Symbol;Acc:HGNC:13415]"}, {"versioned_ensembl_gene_id":"ENSG00000270807.1","gene_symbol":"AC024153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33717853,"end":33718217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113460.12","gene_symbol":"BRIX1","gene_name":"BRX1, biogenesis of ribosomes [Source:HGNC Symbol;Acc:HGNC:24170]","synonyms":"FLJ11100,BXDC2,BRIX","biotype":"protein_coding","ncbi_id":"55299","summary":null,"start":34915376,"end":34925996,"strand":1,"description":"BRX1, biogenesis of ribosomes [Source:HGNC Symbol;Acc:HGNC:24170]"}, {"versioned_ensembl_gene_id":"ENSG00000227542.1","gene_symbol":"AC092614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191229165,"end":191246172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118194.18","gene_symbol":"TNNT2","gene_name":"troponin T2, cardiac type [Source:HGNC Symbol;Acc:HGNC:11949]","synonyms":"CMPD2,CMH2,CMD1D","biotype":"protein_coding","ncbi_id":"7139","summary":"The protein encoded by this gene is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms, however, the full-length nature of some of these variants has not yet been determined. [provided by RefSeq, Jul 2008]","start":201359008,"end":201377762,"strand":-1,"description":"troponin T2, cardiac type [Source:HGNC Symbol;Acc:HGNC:11949]"}, {"versioned_ensembl_gene_id":"ENSG00000108963.17","gene_symbol":"DPH1","gene_name":"diphthamide biosynthesis 1 [Source:HGNC Symbol;Acc:HGNC:3003]","synonyms":"OVCA1,DPH2L1,DPH2L","biotype":"protein_coding","ncbi_id":"1801","summary":"The protein encoded by this gene is an enzyme involved in the biosynthesis of diphthamide, a modified histidine found only in elongation factor-2 (EEF2). Diphthamide residues in EEF2 are targeted for ADP-ribosylation by diphtheria toxin and Pseudomonas exotoxin A. Defects in this gene have been associated with both ovarian cancer and autosomal recessive intellectual disability with short stature, craniofacial, and ectodermal anomalies. [provided by RefSeq, Oct 2016]","start":2030110,"end":2043430,"strand":1,"description":"diphthamide biosynthesis 1 [Source:HGNC Symbol;Acc:HGNC:3003]"}, {"versioned_ensembl_gene_id":"ENSG00000237010.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28897398,"end":28898188,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000268434.5","gene_symbol":"AC011530.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":45779437,"end":45785973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256538.1","gene_symbol":"AC046130.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34037438,"end":34056740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233387.1","gene_symbol":"AL121748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33096257,"end":33116672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197355.10","gene_symbol":"UAP1L1","gene_name":"UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28082]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91373","summary":null,"start":137077501,"end":137084539,"strand":1,"description":"UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28082]"}, {"versioned_ensembl_gene_id":"ENSG00000251802.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":34892417,"end":34892549,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000252920.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":153012482,"end":153012614,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000199088.5","gene_symbol":"MIR379","gene_name":"microRNA 379 [Source:HGNC Symbol;Acc:HGNC:31872]","synonyms":"MIRN379,hsa-mir-379","biotype":"miRNA","ncbi_id":"494328","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101022066,"end":101022132,"strand":1,"description":"microRNA 379 [Source:HGNC Symbol;Acc:HGNC:31872]"}, {"versioned_ensembl_gene_id":"ENSG00000278063.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868122,"end":54868228,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000275254.1","gene_symbol":"FTX_3","gene_name":"FTX transcript, XIST regulator conserved region 3 [Source:RFAM;Acc:RF02121]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74280936,"end":74281082,"strand":1,"description":"FTX transcript, XIST regulator conserved region 3 [Source:RFAM;Acc:RF02121]"}, {"versioned_ensembl_gene_id":"ENSG00000252213.1","gene_symbol":"SNORA74D","gene_name":"small nucleolar RNA, H/ACA box 74D [Source:HGNC Symbol;Acc:HGNC:52219]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616975","summary":null,"start":139276180,"end":139276320,"strand":1,"description":"small nucleolar RNA, H/ACA box 74D [Source:HGNC Symbol;Acc:HGNC:52219]"}, {"versioned_ensembl_gene_id":"ENSG00000265848.1","gene_symbol":"MIR3689D1","gene_name":"microRNA 3689d-1 [Source:HGNC Symbol;Acc:HGNC:41621]","synonyms":"hsa-mir-3689d-1","biotype":"miRNA","ncbi_id":"100616131","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134849609,"end":134849682,"strand":-1,"description":"microRNA 3689d-1 [Source:HGNC Symbol;Acc:HGNC:41621]"}, {"versioned_ensembl_gene_id":"ENSG00000278002.1","gene_symbol":"AL627171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49863072,"end":49864379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274748.1","gene_symbol":"AC233702.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21678086,"end":21678418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284447.1","gene_symbol":"MIR9-2","gene_name":"microRNA 9-2 [Source:HGNC Symbol;Acc:HGNC:31642]","synonyms":"MIRN9-2,hsa-mir-9-2","biotype":"miRNA","ncbi_id":"407047","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88666853,"end":88666939,"strand":-1,"description":"microRNA 9-2 [Source:HGNC Symbol;Acc:HGNC:31642]"}, {"versioned_ensembl_gene_id":"ENSG00000275935.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000278617.1","gene_symbol":"MIR8074","gene_name":"microRNA 8074 [Source:HGNC Symbol;Acc:HGNC:50105]","synonyms":"hsa-mir-8074","biotype":"miRNA","ncbi_id":"102465873","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51206929,"end":51207009,"strand":-1,"description":"microRNA 8074 [Source:HGNC Symbol;Acc:HGNC:50105]"}, {"versioned_ensembl_gene_id":"ENSG00000222418.1","gene_symbol":"RNA5SP113","gene_name":"RNA, 5S ribosomal pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:42911]","synonyms":"RN5S113","biotype":"rRNA","ncbi_id":"100873383","summary":null,"start":182048822,"end":182048905,"strand":1,"description":"RNA, 5S ribosomal pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:42911]"}, {"versioned_ensembl_gene_id":"ENSG00000277153.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54868939,"end":54869045,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000238540.1","gene_symbol":"RNU7-93P","gene_name":"RNA, U7 small nuclear 93 pseudogene [Source:HGNC Symbol;Acc:HGNC:45627]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480813","summary":null,"start":36405214,"end":36405274,"strand":1,"description":"RNA, U7 small nuclear 93 pseudogene [Source:HGNC Symbol;Acc:HGNC:45627]"}, {"versioned_ensembl_gene_id":"ENSG00000283824.1","gene_symbol":"MIR22","gene_name":"microRNA 22 [Source:HGNC Symbol;Acc:HGNC:31599]","synonyms":"MIRN22,hsa-mir-22","biotype":"miRNA","ncbi_id":"407004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1713903,"end":1713987,"strand":-1,"description":"microRNA 22 [Source:HGNC Symbol;Acc:HGNC:31599]"}, {"versioned_ensembl_gene_id":"ENSG00000199005.4","gene_symbol":"MIR370","gene_name":"microRNA 370 [Source:HGNC Symbol;Acc:HGNC:31784]","synonyms":"MIRN370,hsa-mir-370","biotype":"miRNA","ncbi_id":"442915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100911139,"end":100911213,"strand":1,"description":"microRNA 370 [Source:HGNC Symbol;Acc:HGNC:31784]"}, {"versioned_ensembl_gene_id":"ENSG00000275869.1","gene_symbol":"AC136612.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":933862,"end":936467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276094.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":41573512,"end":41573606,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000202514.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42949388,"end":42949495,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000282878.1","gene_symbol":"AC093151.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41242373,"end":41284861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275574.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46833127,"end":46833407,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201510.1","gene_symbol":"RN7SKP217","gene_name":"RNA, 7SK small nuclear pseudogene 217 [Source:HGNC Symbol;Acc:HGNC:45941]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479191","summary":null,"start":76736641,"end":76736980,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 217 [Source:HGNC Symbol;Acc:HGNC:45941]"}, {"versioned_ensembl_gene_id":"ENSG00000281067.1","gene_symbol":"ST13P19","gene_name":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131961","summary":null,"start":210265636,"end":210267241,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]"}, {"versioned_ensembl_gene_id":"ENSG00000260157.3","gene_symbol":"AC233702.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21614487,"end":21641536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263375.1","gene_symbol":"AC233702.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21592794,"end":21594180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198780.11","gene_symbol":"FAM169A","gene_name":"family with sequence similarity 169 member A [Source:HGNC Symbol;Acc:HGNC:29138]","synonyms":"KIAA0888,SLAP75","biotype":"protein_coding","ncbi_id":"26049","summary":null,"start":74777574,"end":74866951,"strand":-1,"description":"family with sequence similarity 169 member A [Source:HGNC Symbol;Acc:HGNC:29138]"}, {"versioned_ensembl_gene_id":"ENSG00000271714.1","gene_symbol":"AC010501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74865893,"end":74867854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150764.13","gene_symbol":"DIXDC1","gene_name":"DIX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23695]","synonyms":"KIAA1735,Dixin","biotype":"protein_coding","ncbi_id":"85458","summary":"The protein encoded by this gene is a positive regulator of the Wnt signaling pathway. The encoded protein is found associated with gamma tubulin at the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]","start":111927144,"end":112022584,"strand":1,"description":"DIX domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23695]"}, {"versioned_ensembl_gene_id":"ENSG00000265370.1","gene_symbol":"MIR4682","gene_name":"microRNA 4682 [Source:HGNC Symbol;Acc:HGNC:41788]","synonyms":"hsa-mir-4682","biotype":"miRNA","ncbi_id":"100616322","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119958513,"end":119958592,"strand":1,"description":"microRNA 4682 [Source:HGNC Symbol;Acc:HGNC:41788]"}, {"versioned_ensembl_gene_id":"ENSG00000207805.3","gene_symbol":"MIR483","gene_name":"microRNA 483 [Source:HGNC Symbol;Acc:HGNC:32340]","synonyms":"MIRN483,hsa-mir-483","biotype":"miRNA","ncbi_id":"619552","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2134134,"end":2134209,"strand":-1,"description":"microRNA 483 [Source:HGNC Symbol;Acc:HGNC:32340]"}, {"versioned_ensembl_gene_id":"ENSG00000207862.1","gene_symbol":"MIR518B","gene_name":"microRNA 518b [Source:HGNC Symbol;Acc:HGNC:32106]","synonyms":"MIRN518B,hsa-mir-518b","biotype":"miRNA","ncbi_id":"574474","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53702737,"end":53702819,"strand":1,"description":"microRNA 518b [Source:HGNC Symbol;Acc:HGNC:32106]"}, {"versioned_ensembl_gene_id":"ENSG00000221792.1","gene_symbol":"MIR1282","gene_name":"microRNA 1282 [Source:HGNC Symbol;Acc:HGNC:35360]","synonyms":"MIRN1282,hsa-mir-1282","biotype":"miRNA","ncbi_id":"100302254","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43793659,"end":43793759,"strand":-1,"description":"microRNA 1282 [Source:HGNC Symbol;Acc:HGNC:35360]"}, {"versioned_ensembl_gene_id":"ENSG00000266593.1","gene_symbol":"MIR4713","gene_name":"microRNA 4713 [Source:HGNC Symbol;Acc:HGNC:41899]","synonyms":"hsa-mir-4713","biotype":"miRNA","ncbi_id":"100616369","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51242190,"end":51242264,"strand":1,"description":"microRNA 4713 [Source:HGNC Symbol;Acc:HGNC:41899]"}, {"versioned_ensembl_gene_id":"ENSG00000207128.1","gene_symbol":"RNU6-729P","gene_name":"RNA, U6 small nuclear 729, pseudogene [Source:HGNC Symbol;Acc:HGNC:47692]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481410","summary":null,"start":10476223,"end":10476329,"strand":1,"description":"RNA, U6 small nuclear 729, pseudogene [Source:HGNC Symbol;Acc:HGNC:47692]"}, {"versioned_ensembl_gene_id":"ENSG00000199730.1","gene_symbol":"RN7SKP95","gene_name":"RNA, 7SK small nuclear pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:45819]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480862","summary":null,"start":58703852,"end":58704154,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:45819]"}, {"versioned_ensembl_gene_id":"ENSG00000212145.2","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":41899111,"end":41899253,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000207308.1","gene_symbol":"RNU6-878P","gene_name":"RNA, U6 small nuclear 878, pseudogene [Source:HGNC Symbol;Acc:HGNC:47841]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479954","summary":null,"start":2321718,"end":2321827,"strand":1,"description":"RNA, U6 small nuclear 878, pseudogene [Source:HGNC Symbol;Acc:HGNC:47841]"}, {"versioned_ensembl_gene_id":"ENSG00000221697.1","gene_symbol":"MIR1275","gene_name":"microRNA 1275 [Source:HGNC Symbol;Acc:HGNC:35346]","synonyms":"MIRN1275,hsa-mir-1275","biotype":"miRNA","ncbi_id":"100302123","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33999972,"end":34000051,"strand":-1,"description":"microRNA 1275 [Source:HGNC Symbol;Acc:HGNC:35346]"}, {"versioned_ensembl_gene_id":"ENSG00000211520.2","gene_symbol":"MIR216B","gene_name":"microRNA 216b [Source:HGNC Symbol;Acc:HGNC:33668]","synonyms":"MIRN216B,hsa-mir-216b","biotype":"miRNA","ncbi_id":"100126319","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56000714,"end":56000795,"strand":-1,"description":"microRNA 216b [Source:HGNC Symbol;Acc:HGNC:33668]"}, {"versioned_ensembl_gene_id":"ENSG00000278422.1","gene_symbol":"RN7SL331P","gene_name":"RNA, 7SL, cytoplasmic 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:46347]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479344","summary":null,"start":84205454,"end":84205700,"strand":-1,"description":"RNA, 7SL, cytoplasmic 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:46347]"}, {"versioned_ensembl_gene_id":"ENSG00000208009.1","gene_symbol":"MIR130A","gene_name":"microRNA 130a [Source:HGNC Symbol;Acc:HGNC:31514]","synonyms":"MIRN130A,hsa-mir-130a","biotype":"miRNA","ncbi_id":"406919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57641198,"end":57641286,"strand":1,"description":"microRNA 130a [Source:HGNC Symbol;Acc:HGNC:31514]"}, {"versioned_ensembl_gene_id":"ENSG00000281420.1","gene_symbol":"AP001052.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":43748365,"end":43748468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277856.1","gene_symbol":"AC233755.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":26241,"end":26534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199311.1","gene_symbol":"SNORD115-34","gene_name":"small nucleolar RNA, C/D box 115-34 [Source:HGNC Symbol;Acc:HGNC:33053]","synonyms":"HBII-52-34","biotype":"snoRNA","ncbi_id":"100033808","summary":null,"start":25232387,"end":25232468,"strand":1,"description":"small nucleolar RNA, C/D box 115-34 [Source:HGNC Symbol;Acc:HGNC:33053]"}, {"versioned_ensembl_gene_id":"ENSG00000200638.1","gene_symbol":"SNORD115-37","gene_name":"small nucleolar RNA, C/D box 115-37 [Source:HGNC Symbol;Acc:HGNC:33056]","synonyms":"HBII-52-37","biotype":"snoRNA","ncbi_id":"100033811","summary":null,"start":25237986,"end":25238067,"strand":1,"description":"small nucleolar RNA, C/D box 115-37 [Source:HGNC Symbol;Acc:HGNC:33056]"}, {"versioned_ensembl_gene_id":"ENSG00000283592.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29575060,"end":29575171,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242673.3","gene_symbol":"RN7SL167P","gene_name":"RNA, 7SL, cytoplasmic 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:46183]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480966","summary":null,"start":131004128,"end":131004429,"strand":-1,"description":"RNA, 7SL, cytoplasmic 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:46183]"}, {"versioned_ensembl_gene_id":"ENSG00000265223.1","gene_symbol":"RNU1-79P","gene_name":"RNA, U1 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:48421]","synonyms":null,"biotype":"snRNA","ncbi_id":"107521942","summary":null,"start":32441551,"end":32441699,"strand":-1,"description":"RNA, U1 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:48421]"}, {"versioned_ensembl_gene_id":"ENSG00000243124.3","gene_symbol":"RN7SL643P","gene_name":"RNA, 7SL, cytoplasmic 643, pseudogene [Source:HGNC Symbol;Acc:HGNC:46659]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481098","summary":null,"start":86435848,"end":86436138,"strand":1,"description":"RNA, 7SL, cytoplasmic 643, pseudogene [Source:HGNC Symbol;Acc:HGNC:46659]"}, {"versioned_ensembl_gene_id":"ENSG00000274574.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":144560668,"end":144560831,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000283372.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":98026042,"end":98026139,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207389.1","gene_symbol":"RNU1-4","gene_name":"RNA, U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:10128]","synonyms":"U1F,U1E2,U1D2,U1B2,RNU1G2,RNU1G1,RNU1F1,RNU1E2,RNU1D2,HSD7,HSD6,HSD5,HSD2","biotype":"snRNA","ncbi_id":"6060","summary":null,"start":16740516,"end":16740679,"strand":1,"description":"RNA, U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:10128]"}, {"versioned_ensembl_gene_id":"ENSG00000277818.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":79562745,"end":79562846,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252686.1","gene_symbol":"RNU6-1234P","gene_name":"RNA, U6 small nuclear 1234, pseudogene [Source:HGNC Symbol;Acc:HGNC:48197]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480106","summary":null,"start":29811916,"end":29812018,"strand":1,"description":"RNA, U6 small nuclear 1234, pseudogene [Source:HGNC Symbol;Acc:HGNC:48197]"}, {"versioned_ensembl_gene_id":"ENSG00000221475.1","gene_symbol":"SNORA11D","gene_name":"small nucleolar RNA, H/ACA box 11D [Source:HGNC Symbol;Acc:HGNC:33622]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124541","summary":null,"start":52190621,"end":52190748,"strand":1,"description":"small nucleolar RNA, H/ACA box 11D [Source:HGNC Symbol;Acc:HGNC:33622]"}, {"versioned_ensembl_gene_id":"ENSG00000207330.1","gene_symbol":"RNU6-73P","gene_name":"RNA, U6 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:42563]","synonyms":"RNU6-73","biotype":"snRNA","ncbi_id":"106478989","summary":null,"start":27828763,"end":27828869,"strand":1,"description":"RNA, U6 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:42563]"}, {"versioned_ensembl_gene_id":"ENSG00000206679.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":95125511,"end":95125609,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265237.1","gene_symbol":"MIR3142","gene_name":"microRNA 3142 [Source:HGNC Symbol;Acc:HGNC:38297]","synonyms":"hsa-mir-3142","biotype":"miRNA","ncbi_id":"100422938","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160474402,"end":160474483,"strand":1,"description":"microRNA 3142 [Source:HGNC Symbol;Acc:HGNC:38297]"}, {"versioned_ensembl_gene_id":"ENSG00000171617.13","gene_symbol":"ENC1","gene_name":"ectodermal-neural cortex 1 [Source:HGNC Symbol;Acc:HGNC:3345]","synonyms":"TP53I10,PIG10,NRPB,KLHL37,ENC-1","biotype":"protein_coding","ncbi_id":"8507","summary":"This gene encodes a member of the kelch-related family of actin-binding proteins. The encoded protein plays a role in the oxidative stress response as a regulator of the transcription factor Nrf2, and expression of this gene may play a role in malignant transformation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":74627406,"end":74641424,"strand":-1,"description":"ectodermal-neural cortex 1 [Source:HGNC Symbol;Acc:HGNC:3345]"}, {"versioned_ensembl_gene_id":"ENSG00000231057.3","gene_symbol":"AC096637.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":211675762,"end":211690103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251076.1","gene_symbol":"AC104126.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112228283,"end":112257309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238901.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":122671291,"end":122671394,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000275843.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"NALP2,PYPAF2,NBS1,CLR19.9,FLJ20510,NBS1,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54998440,"end":55034296,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000277666.1","gene_symbol":"AC136352.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":100123,"end":101141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199731.1","gene_symbol":"RNU6-1079P","gene_name":"RNA, U6 small nuclear 1079, pseudogene [Source:HGNC Symbol;Acc:HGNC:48042]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480040","summary":null,"start":32234766,"end":32234875,"strand":-1,"description":"RNA, U6 small nuclear 1079, pseudogene [Source:HGNC Symbol;Acc:HGNC:48042]"}, {"versioned_ensembl_gene_id":"ENSG00000241406.3","gene_symbol":"RN7SL515P","gene_name":"RNA, 7SL, cytoplasmic 515, pseudogene [Source:HGNC Symbol;Acc:HGNC:46531]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481063","summary":null,"start":41807677,"end":41807973,"strand":1,"description":"RNA, 7SL, cytoplasmic 515, pseudogene [Source:HGNC Symbol;Acc:HGNC:46531]"}, {"versioned_ensembl_gene_id":"ENSG00000202189.1","gene_symbol":"SNORA30B","gene_name":"small nucleolar RNA, H/ACA box 30B [Source:HGNC Symbol;Acc:HGNC:52200]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616992","summary":null,"start":20786927,"end":20787055,"strand":1,"description":"small nucleolar RNA, H/ACA box 30B [Source:HGNC Symbol;Acc:HGNC:52200]"}, {"versioned_ensembl_gene_id":"ENSG00000200367.1","gene_symbol":"SNORD113-8","gene_name":"small nucleolar RNA, C/D box 113-8 [Source:HGNC Symbol;Acc:HGNC:32987]","synonyms":"14q(I-8)","biotype":"snoRNA","ncbi_id":"767568","summary":null,"start":100943451,"end":100943524,"strand":1,"description":"small nucleolar RNA, C/D box 113-8 [Source:HGNC Symbol;Acc:HGNC:32987]"}, {"versioned_ensembl_gene_id":"ENSG00000278328.1","gene_symbol":"MIR6802","gene_name":"microRNA 6802 [Source:HGNC Symbol;Acc:HGNC:50154]","synonyms":"hsa-mir-6802","biotype":"miRNA","ncbi_id":"102465481","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55239912,"end":55239976,"strand":-1,"description":"microRNA 6802 [Source:HGNC Symbol;Acc:HGNC:50154]"}, {"versioned_ensembl_gene_id":"ENSG00000274841.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":137638128,"end":137638408,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275696.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":186629936,"end":186630211,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212495.1","gene_symbol":"RNU6-332P","gene_name":"RNA, U6 small nuclear 332, pseudogene [Source:HGNC Symbol;Acc:HGNC:47295]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481284","summary":null,"start":94003815,"end":94003922,"strand":-1,"description":"RNA, U6 small nuclear 332, pseudogene [Source:HGNC Symbol;Acc:HGNC:47295]"}, {"versioned_ensembl_gene_id":"ENSG00000200872.1","gene_symbol":"RNA5SP456","gene_name":"RNA, 5S ribosomal pseudogene 456 [Source:HGNC Symbol;Acc:HGNC:43356]","synonyms":"RN5S456","biotype":"rRNA","ncbi_id":"100873701","summary":null,"start":48475487,"end":48475600,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 456 [Source:HGNC Symbol;Acc:HGNC:43356]"}, {"versioned_ensembl_gene_id":"ENSG00000274597.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54940339,"end":54940445,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000263419.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28974068,"end":28974366,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207634.1","gene_symbol":"MIR521-1","gene_name":"microRNA 521-1 [Source:HGNC Symbol;Acc:HGNC:32126]","synonyms":"MIRN521-1,hsa-mir-521-1","biotype":"miRNA","ncbi_id":"574494","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53748636,"end":53748722,"strand":1,"description":"microRNA 521-1 [Source:HGNC Symbol;Acc:HGNC:32126]"}, {"versioned_ensembl_gene_id":"ENSG00000221545.1","gene_symbol":"MIR1255B2","gene_name":"microRNA 1255b-2 [Source:HGNC Symbol;Acc:HGNC:35367]","synonyms":"MIRN1255B2,hsa-mir-1255b-2","biotype":"miRNA","ncbi_id":"100313835","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":167998660,"end":167998726,"strand":1,"description":"microRNA 1255b-2 [Source:HGNC Symbol;Acc:HGNC:35367]"}, {"versioned_ensembl_gene_id":"ENSG00000206723.1","gene_symbol":"RNU6-1056P","gene_name":"RNA, U6 small nuclear 1056, pseudogene [Source:HGNC Symbol;Acc:HGNC:48019]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481514","summary":null,"start":48724455,"end":48724561,"strand":-1,"description":"RNA, U6 small nuclear 1056, pseudogene [Source:HGNC Symbol;Acc:HGNC:48019]"}, {"versioned_ensembl_gene_id":"ENSG00000252067.1","gene_symbol":"RNU4-71P","gene_name":"RNA, U4 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:47007]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481194","summary":null,"start":23600026,"end":23600138,"strand":-1,"description":"RNA, U4 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:47007]"}, {"versioned_ensembl_gene_id":"ENSG00000229654.1","gene_symbol":"LINC02526","gene_name":"long intergenic non-protein coding RNA 2526 [Source:HGNC Symbol;Acc:HGNC:53550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377926","summary":null,"start":106695535,"end":106699994,"strand":1,"description":"long intergenic non-protein coding RNA 2526 [Source:HGNC Symbol;Acc:HGNC:53550]"}, {"versioned_ensembl_gene_id":"ENSG00000267614.1","gene_symbol":"AC245748.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44536263,"end":44536613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275527.1","gene_symbol":"AC100835.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74598919,"end":74599397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221649.1","gene_symbol":"MIR1233-1","gene_name":"microRNA 1233-1 [Source:HGNC Symbol;Acc:HGNC:33929]","synonyms":"MIRN1233,MIR1233,hsa-mir-1233","biotype":"miRNA","ncbi_id":"100302160","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34382069,"end":34382150,"strand":-1,"description":"microRNA 1233-1 [Source:HGNC Symbol;Acc:HGNC:33929]"}, {"versioned_ensembl_gene_id":"ENSG00000207500.1","gene_symbol":"SNORD102","gene_name":"small nucleolar RNA, C/D box 102 [Source:HGNC Symbol;Acc:HGNC:10099]","synonyms":"U102,RNU102","biotype":"snoRNA","ncbi_id":"26771","summary":null,"start":27255064,"end":27255135,"strand":1,"description":"small nucleolar RNA, C/D box 102 [Source:HGNC Symbol;Acc:HGNC:10099]"}, {"versioned_ensembl_gene_id":"ENSG00000274822.1","gene_symbol":"MIR6762","gene_name":"microRNA 6762 [Source:HGNC Symbol;Acc:HGNC:50168]","synonyms":"hsa-mir-6762","biotype":"miRNA","ncbi_id":"102465457","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113291523,"end":113291608,"strand":1,"description":"microRNA 6762 [Source:HGNC Symbol;Acc:HGNC:50168]"}, {"versioned_ensembl_gene_id":"ENSG00000276150.1","gene_symbol":"TTC28-AS1_2","gene_name":"TTC28 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02199]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27922022,"end":27922178,"strand":1,"description":"TTC28 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02199]"}, {"versioned_ensembl_gene_id":"ENSG00000200597.1","gene_symbol":"RNU1-87P","gene_name":"RNA, U1 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:48429]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480178","summary":null,"start":37915573,"end":37915742,"strand":1,"description":"RNA, U1 small nuclear 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:48429]"}, {"versioned_ensembl_gene_id":"ENSG00000207062.1","gene_symbol":"SNORA15B-1","gene_name":"small nucleolar RNA, H/ACA box 15B-1 [Source:HGNC Symbol;Acc:HGNC:52191]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616962","summary":null,"start":65070538,"end":65070672,"strand":1,"description":"small nucleolar RNA, H/ACA box 15B-1 [Source:HGNC Symbol;Acc:HGNC:52191]"}, {"versioned_ensembl_gene_id":"ENSG00000274884.1","gene_symbol":"AL117190.3","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100826284,"end":100826370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243991.3","gene_symbol":"RN7SL447P","gene_name":"RNA, 7SL, cytoplasmic 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:46463]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479386","summary":null,"start":193740471,"end":193740715,"strand":-1,"description":"RNA, 7SL, cytoplasmic 447, pseudogene [Source:HGNC Symbol;Acc:HGNC:46463]"}, {"versioned_ensembl_gene_id":"ENSG00000206675.1","gene_symbol":"RNU6-32P","gene_name":"RNA, U6 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:34276]","synonyms":"RNU6-32","biotype":"snRNA","ncbi_id":"106480708","summary":null,"start":39297605,"end":39297711,"strand":-1,"description":"RNA, U6 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:34276]"}, {"versioned_ensembl_gene_id":"ENSG00000206692.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":171253906,"end":171254022,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264073.1","gene_symbol":"MIR3199-1","gene_name":"microRNA 3199-1 [Source:HGNC Symbol;Acc:HGNC:38294]","synonyms":"hsa-mir-3199-1","biotype":"miRNA","ncbi_id":"100423034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27920525,"end":27920612,"strand":-1,"description":"microRNA 3199-1 [Source:HGNC Symbol;Acc:HGNC:38294]"}, {"versioned_ensembl_gene_id":"ENSG00000252279.1","gene_symbol":"RNU6-406P","gene_name":"RNA, U6 small nuclear 406, pseudogene [Source:HGNC Symbol;Acc:HGNC:47369]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481306","summary":null,"start":43445507,"end":43445613,"strand":1,"description":"RNA, U6 small nuclear 406, pseudogene [Source:HGNC Symbol;Acc:HGNC:47369]"}, {"versioned_ensembl_gene_id":"ENSG00000202058.1","gene_symbol":"RN7SKP80","gene_name":"RNA, 7SK small nuclear pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:45804]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479130","summary":null,"start":42565048,"end":42565330,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:45804]"}, {"versioned_ensembl_gene_id":"ENSG00000221365.1","gene_symbol":"MIR1228","gene_name":"microRNA 1228 [Source:HGNC Symbol;Acc:HGNC:33928]","synonyms":"MIRN1228,hsa-mir-1228","biotype":"miRNA","ncbi_id":"100302201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57194504,"end":57194576,"strand":1,"description":"microRNA 1228 [Source:HGNC Symbol;Acc:HGNC:33928]"}, {"versioned_ensembl_gene_id":"ENSG00000266308.2","gene_symbol":"RN7SL510P","gene_name":"RNA, 7SL, cytoplasmic 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:46526]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479410","summary":null,"start":75895040,"end":75895302,"strand":1,"description":"RNA, 7SL, cytoplasmic 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:46526]"}, {"versioned_ensembl_gene_id":"ENSG00000201547.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67408774,"end":67408881,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240151.3","gene_symbol":"RN7SL826P","gene_name":"RNA, 7SL, cytoplasmic 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:46842]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479523","summary":null,"start":117163968,"end":117164255,"strand":1,"description":"RNA, 7SL, cytoplasmic 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:46842]"}, {"versioned_ensembl_gene_id":"ENSG00000200555.1","gene_symbol":"RNU6-525P","gene_name":"RNA, U6 small nuclear 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:47488]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479799","summary":null,"start":180444509,"end":180444612,"strand":1,"description":"RNA, U6 small nuclear 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:47488]"}, {"versioned_ensembl_gene_id":"ENSG00000260679.1","gene_symbol":"AP007216.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69921638,"end":69926813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269236.1","gene_symbol":"AC008751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58166166,"end":58167145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276584.1","gene_symbol":"MIR6737","gene_name":"microRNA 6737 [Source:HGNC Symbol;Acc:HGNC:50273]","synonyms":"hsa-mir-6737","biotype":"miRNA","ncbi_id":"102465441","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153962351,"end":153962420,"strand":-1,"description":"microRNA 6737 [Source:HGNC Symbol;Acc:HGNC:50273]"}, {"versioned_ensembl_gene_id":"ENSG00000212497.1","gene_symbol":"RNA5SP465","gene_name":"RNA, 5S ribosomal pseudogene 465 [Source:HGNC Symbol;Acc:HGNC:43365]","synonyms":"RN5S465","biotype":"rRNA","ncbi_id":"100873709","summary":null,"start":12027913,"end":12028021,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 465 [Source:HGNC Symbol;Acc:HGNC:43365]"}, {"versioned_ensembl_gene_id":"ENSG00000277359.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000251861.1","gene_symbol":"SCARNA20","gene_name":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]","synonyms":"ACA66","biotype":"scaRNA","ncbi_id":"677681","summary":null,"start":204727991,"end":204728106,"strand":1,"description":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]"}, {"versioned_ensembl_gene_id":"ENSG00000278050.1","gene_symbol":"NEAT1_2","gene_name":"Nuclear enriched abundant transcript 1 conserved region 2 [Source:RFAM;Acc:RF01956]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65423638,"end":65423742,"strand":1,"description":"Nuclear enriched abundant transcript 1 conserved region 2 [Source:RFAM;Acc:RF01956]"}, {"versioned_ensembl_gene_id":"ENSG00000264163.1","gene_symbol":"MIR3689B","gene_name":"microRNA 3689b [Source:HGNC Symbol;Acc:HGNC:38924]","synonyms":"hsa-mir-3689b","biotype":"miRNA","ncbi_id":"100500906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850125,"end":134850272,"strand":-1,"description":"microRNA 3689b [Source:HGNC Symbol;Acc:HGNC:38924]"}, {"versioned_ensembl_gene_id":"ENSG00000265247.1","gene_symbol":"MIR4472-1","gene_name":"microRNA 4472-1 [Source:HGNC Symbol;Acc:HGNC:41644]","synonyms":"hsa-mir-4472-1","biotype":"miRNA","ncbi_id":"100616268","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":142176339,"end":142176418,"strand":1,"description":"microRNA 4472-1 [Source:HGNC Symbol;Acc:HGNC:41644]"}, {"versioned_ensembl_gene_id":"ENSG00000283298.1","gene_symbol":"MIR4272","gene_name":"microRNA 4272 [Source:HGNC Symbol;Acc:HGNC:38303]","synonyms":"hsa-mir-4272","biotype":"miRNA","ncbi_id":"100422941","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67225464,"end":67225527,"strand":1,"description":"microRNA 4272 [Source:HGNC Symbol;Acc:HGNC:38303]"}, {"versioned_ensembl_gene_id":"ENSG00000283764.1","gene_symbol":"MIR6850","gene_name":"microRNA 6850 [Source:HGNC Symbol;Acc:HGNC:50093]","synonyms":"hsa-mir-6850","biotype":"miRNA","ncbi_id":"102465978","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144791931,"end":144791991,"strand":-1,"description":"microRNA 6850 [Source:HGNC Symbol;Acc:HGNC:50093]"}, {"versioned_ensembl_gene_id":"ENSG00000284328.1","gene_symbol":"AC132825.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22531876,"end":22532172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284263.1","gene_symbol":"AC132825.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22532166,"end":22532522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266691.1","gene_symbol":"AC138761.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22277867,"end":22279289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282885.1","gene_symbol":"AL627171.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49861176,"end":49864326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164347.17","gene_symbol":"GFM2","gene_name":"G elongation factor mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:29682]","synonyms":"FLJ21661,EFG2","biotype":"protein_coding","ncbi_id":"84340","summary":"Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA . Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]","start":74721204,"end":74767371,"strand":-1,"description":"G elongation factor mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:29682]"}, {"versioned_ensembl_gene_id":"ENSG00000264245.1","gene_symbol":"AC233702.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21573770,"end":21574073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266673.1","gene_symbol":"AC233702.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21552509,"end":21552711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266466.1","gene_symbol":"AC233702.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21532974,"end":21542786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173653.7","gene_symbol":"RCE1","gene_name":"Ras converting CAAX endopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:13721]","synonyms":"RCE1B,RCE1A,hRCE1,FACE2,FACE-2","biotype":"protein_coding","ncbi_id":"9986","summary":"This gene encodes an integral membrane protein which is classified as a member of the metalloproteinase family. This enzyme is thought to function in the maintenance and processing of CAAX-type prenylated proteins. [provided by RefSeq, Jul 2008]","start":66842835,"end":66846546,"strand":1,"description":"Ras converting CAAX endopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:13721]"}, {"versioned_ensembl_gene_id":"ENSG00000278910.3","gene_symbol":"BANCR","gene_name":"BRAF-activated non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:43877]","synonyms":"LINC00586","biotype":"lincRNA","ncbi_id":"100885775","summary":"This gene produces a long non-coding RNA that plays a role in tumor progression and epithelial to mesenchymal transition. This transcript acts through the MAP kinase signaling pathway. [provided by RefSeq, Dec 2017]","start":69296682,"end":69306977,"strand":-1,"description":"BRAF-activated non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:43877]"}, {"versioned_ensembl_gene_id":"ENSG00000135063.17","gene_symbol":"FAM189A2","gene_name":"family with sequence similarity 189 member A2 [Source:HGNC Symbol;Acc:HGNC:24820]","synonyms":"X123,C9orf61","biotype":"protein_coding","ncbi_id":"9413","summary":null,"start":69324572,"end":69392455,"strand":1,"description":"family with sequence similarity 189 member A2 [Source:HGNC Symbol;Acc:HGNC:24820]"}, {"versioned_ensembl_gene_id":"ENSG00000196405.12","gene_symbol":"EVL","gene_name":"Enah/Vasp-like [Source:HGNC Symbol;Acc:HGNC:20234]","synonyms":"RNB6","biotype":"protein_coding","ncbi_id":"51466","summary":null,"start":99971449,"end":100144236,"strand":1,"description":"Enah/Vasp-like [Source:HGNC Symbol;Acc:HGNC:20234]"}, {"versioned_ensembl_gene_id":"ENSG00000258693.1","gene_symbol":"AL133368.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99977115,"end":99978098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196387.9","gene_symbol":"ZNF140","gene_name":"zinc finger protein 140 [Source:HGNC Symbol;Acc:HGNC:12925]","synonyms":"pHZ-39","biotype":"protein_coding","ncbi_id":"7699","summary":null,"start":133079838,"end":133107544,"strand":1,"description":"zinc finger protein 140 [Source:HGNC Symbol;Acc:HGNC:12925]"}, {"versioned_ensembl_gene_id":"ENSG00000279466.1","gene_symbol":"AC073911.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133073516,"end":133073983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232728.1","gene_symbol":"PHB2P1","gene_name":"prohibitin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645318","summary":null,"start":109528119,"end":109529008,"strand":1,"description":"prohibitin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45249]"}, {"versioned_ensembl_gene_id":"ENSG00000224498.1","gene_symbol":"MAPKAPK5P1","gene_name":"mitogen-activated protein kinase-activated protein kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45246]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533849","summary":null,"start":108848186,"end":108849561,"strand":1,"description":"mitogen-activated protein kinase-activated protein kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45246]"}, {"versioned_ensembl_gene_id":"ENSG00000234544.2","gene_symbol":"PTGES3P5","gene_name":"prostaglandin E synthase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480359","summary":null,"start":108296099,"end":108296532,"strand":1,"description":"prostaglandin E synthase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43826]"}, {"versioned_ensembl_gene_id":"ENSG00000136878.12","gene_symbol":"USP20","gene_name":"ubiquitin specific peptidase 20 [Source:HGNC Symbol;Acc:HGNC:12619]","synonyms":"KIAA1003","biotype":"protein_coding","ncbi_id":"10868","summary":"This gene encodes a ubiquitin specific processing protease that was first identified as a substrate of the VHL (von Hippel-Lindau disease) protein E3 ubiquitin ligase complex. In addition to being ubiquitinated by the VHL-E3 ligase complex, this enzyme deubiquitinates hypoxia-inducible factor (HIF)-1 alpha and thereby causes increased expression of HIF-1alpha targeted genes which play a role in angiogenesis, glucose metabolism, cell proliferation and metastasis. The enzyme encoded by this gene also regulates G-protein coupled receptor signaling by mediating the deubiquitination of beta-2 adrenergic receptor (ADRB2). This enzyme is a ubiquitously expressed thiolester hydrolase. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jan 2013]","start":129834698,"end":129881838,"strand":1,"description":"ubiquitin specific peptidase 20 [Source:HGNC Symbol;Acc:HGNC:12619]"}, {"versioned_ensembl_gene_id":"ENSG00000136819.15","gene_symbol":"C9orf78","gene_name":"chromosome 9 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:24932]","synonyms":"HSPC220,HCA59","biotype":"protein_coding","ncbi_id":"51759","summary":null,"start":129827290,"end":129835863,"strand":-1,"description":"chromosome 9 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:24932]"}, {"versioned_ensembl_gene_id":"ENSG00000234528.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SUMO2P,SMT3Bp,dJ271M21,SMT3H2P","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29635969,"end":29636252,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000259058.1","gene_symbol":"AF111169.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76921840,"end":76924649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213201.3","gene_symbol":"FABP5P10","gene_name":"fatty acid binding protein 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31066]","synonyms":"FABP5L10","biotype":"processed_pseudogene","ncbi_id":"344332","summary":null,"start":151186188,"end":151186595,"strand":1,"description":"fatty acid binding protein 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31066]"}, {"versioned_ensembl_gene_id":"ENSG00000234789.1","gene_symbol":"AL590369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129640476,"end":129641282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228510.2","gene_symbol":"AL359091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128444587,"end":128446628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233626.2","gene_symbol":"AC092814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211936249,"end":211936634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225385.3","gene_symbol":"AL353572.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88066915,"end":88068037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204277.1","gene_symbol":"LINC01993","gene_name":"long intergenic non-protein coding RNA 1993 [Source:HGNC Symbol;Acc:HGNC:52826]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996291","summary":null,"start":78261349,"end":78278492,"strand":-1,"description":"long intergenic non-protein coding RNA 1993 [Source:HGNC Symbol;Acc:HGNC:52826]"}, {"versioned_ensembl_gene_id":"ENSG00000267737.1","gene_symbol":"AC087645.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78315729,"end":78347798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267676.1","gene_symbol":"THA1P","gene_name":"threonine aldolase 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18004]","synonyms":"GLY1","biotype":"unitary_pseudogene","ncbi_id":"390816","summary":null,"start":78248493,"end":78254416,"strand":-1,"description":"threonine aldolase 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18004]"}, {"versioned_ensembl_gene_id":"ENSG00000283914.1","gene_symbol":"AC087645.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78248193,"end":78251440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178217.13","gene_symbol":"SH2D4B","gene_name":"SH2 domain containing 4B [Source:HGNC Symbol;Acc:HGNC:31440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387694","summary":null,"start":80537902,"end":80646560,"strand":1,"description":"SH2 domain containing 4B [Source:HGNC Symbol;Acc:HGNC:31440]"}, {"versioned_ensembl_gene_id":"ENSG00000204054.13","gene_symbol":"LINC00963","gene_name":"long intergenic non-protein coding RNA 963 [Source:HGNC Symbol;Acc:HGNC:48716]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506190","summary":null,"start":129483451,"end":129513686,"strand":1,"description":"long intergenic non-protein coding RNA 963 [Source:HGNC Symbol;Acc:HGNC:48716]"}, {"versioned_ensembl_gene_id":"ENSG00000254978.2","gene_symbol":"ALG1L9P","gene_name":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44378]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285407","summary":null,"start":71800541,"end":71804640,"strand":-1,"description":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44378]"}, {"versioned_ensembl_gene_id":"ENSG00000260422.1","gene_symbol":"Z97205.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164084023,"end":164085661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272774.1","gene_symbol":"AC112219.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72178279,"end":72178810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254186.1","gene_symbol":"AC091901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162558685,"end":162623461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255319.5","gene_symbol":"ENPP7P8","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48691]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421860","summary":null,"start":71711740,"end":71781183,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48691]"}, {"versioned_ensembl_gene_id":"ENSG00000214144.3","gene_symbol":"AL390728.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247229940,"end":247231880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251187.5","gene_symbol":"AC010261.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112192020,"end":112210139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261334.1","gene_symbol":"AL353803.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129480605,"end":129482538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108639.7","gene_symbol":"SYNGR2","gene_name":"synaptogyrin 2 [Source:HGNC Symbol;Acc:HGNC:11499]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9144","summary":"This gene encodes an integral membrane protein containing four transmembrane regions and a C-terminal cytoplasmic tail that is tyrosine phosphorylated. The exact function of this protein is unclear, but studies of a similar rat protein suggest that it may play a role in regulating membrane traffic in non-neuronal cells. The gene belongs to the synaptogyrin gene family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":78168558,"end":78173527,"strand":1,"description":"synaptogyrin 2 [Source:HGNC Symbol;Acc:HGNC:11499]"}, {"versioned_ensembl_gene_id":"ENSG00000166851.14","gene_symbol":"PLK1","gene_name":"polo like kinase 1 [Source:HGNC Symbol;Acc:HGNC:9077]","synonyms":"PLK","biotype":"protein_coding","ncbi_id":"5347","summary":"The Ser/Thr protein kinase encoded by this gene belongs to the CDC5/Polo subfamily. It is highly expressed during mitosis and elevated levels are found in many different types of cancer. Depletion of this protein in cancer cells dramatically inhibited cell proliferation and induced apoptosis; hence, it is a target for cancer therapy. [provided by RefSeq, Sep 2015]","start":23677656,"end":23690367,"strand":1,"description":"polo like kinase 1 [Source:HGNC Symbol;Acc:HGNC:9077]"}, {"versioned_ensembl_gene_id":"ENSG00000170909.13","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094668,"end":54102692,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000255261.1","gene_symbol":"OR7E4P","gene_name":"olfactory receptor family 7 subfamily E member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8424]","synonyms":"OR7F4P,OR11-11a","biotype":"unprocessed_pseudogene","ncbi_id":"8585","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71620020,"end":71621032,"strand":1,"description":"olfactory receptor family 7 subfamily E member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8424]"}, {"versioned_ensembl_gene_id":"ENSG00000117650.12","gene_symbol":"NEK2","gene_name":"NIMA related kinase 2 [Source:HGNC Symbol;Acc:HGNC:7745]","synonyms":"RP67,PPP1R111,NLK1,NEK2A","biotype":"protein_coding","ncbi_id":"4751","summary":"This gene encodes a serine/threonine-protein kinase that is involved in mitotic regulation. This protein is localized to the centrosome, and undetectable during G1 phase, but accumulates progressively throughout the S phase, reaching maximal levels in late G2 phase. Alternatively spliced transcript variants encoding different isoforms with distinct C-termini have been noted for this gene. [provided by RefSeq, Feb 2011]","start":211658657,"end":211675630,"strand":-1,"description":"NIMA related kinase 2 [Source:HGNC Symbol;Acc:HGNC:7745]"}, {"versioned_ensembl_gene_id":"ENSG00000134398.14","gene_symbol":"ERN2","gene_name":"endoplasmic reticulum to nucleus signaling 2 [Source:HGNC Symbol;Acc:HGNC:16942]","synonyms":"IRE1b","biotype":"protein_coding","ncbi_id":"10595","summary":null,"start":23690326,"end":23713500,"strand":-1,"description":"endoplasmic reticulum to nucleus signaling 2 [Source:HGNC Symbol;Acc:HGNC:16942]"}, {"versioned_ensembl_gene_id":"ENSG00000147676.13","gene_symbol":"MAL2","gene_name":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114569","summary":"This gene encodes a multispan transmembrane protein belonging to the MAL proteolipid family. The protein is a component of lipid rafts and, in polarized cells, it primarily localizes to endosomal structures beneath the apical membrane. It is required for transcytosis, an intracellular transport pathway used to deliver membrane-bound proteins and exogenous cargos from the basolateral to the apical surface. [provided by RefSeq, Jul 2008]","start":119165034,"end":119245673,"strand":1,"description":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]"}, {"versioned_ensembl_gene_id":"ENSG00000105281.12","gene_symbol":"SLC1A5","gene_name":"solute carrier family 1 member 5 [Source:HGNC Symbol;Acc:HGNC:10943]","synonyms":"RDRC,M7V1,ASCT2,AAAT","biotype":"protein_coding","ncbi_id":"6510","summary":"The SLC1A5 gene encodes a sodium-dependent neutral amino acid transporter that can act as a receptor for RD114/type D retrovirus (Larriba et al., 2001 [PubMed 11781704]).[supplied by OMIM, Jan 2011]","start":46774883,"end":46788594,"strand":-1,"description":"solute carrier family 1 member 5 [Source:HGNC Symbol;Acc:HGNC:10943]"}, {"versioned_ensembl_gene_id":"ENSG00000250699.1","gene_symbol":"AP000892.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117316362,"end":117328038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271412.1","gene_symbol":"PRR13P3","gene_name":"proline rich 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129201","summary":null,"start":117336256,"end":117336631,"strand":-1,"description":"proline rich 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50616]"}, {"versioned_ensembl_gene_id":"ENSG00000254278.1","gene_symbol":"AC107953.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119062942,"end":119068782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184374.2","gene_symbol":"COLEC10","gene_name":"collectin subfamily member 10 [Source:HGNC Symbol;Acc:HGNC:2220]","synonyms":"CL-L1","biotype":"protein_coding","ncbi_id":"10584","summary":"This gene encodes a member of the C-lectin family, proteins that possess collagen-like sequences and carbohydrate recognition domains. The other members of this family are secreted proteins and bind to carbohydrate antigens on microorganisms facilitating their recognition and removal. This gene product is a cytosolic protein, a characteristic that suggests that it may have different biological functions than other C-lectins. [provided by RefSeq, Jul 2008]","start":118995452,"end":119106582,"strand":1,"description":"collectin subfamily member 10 [Source:HGNC Symbol;Acc:HGNC:2220]"}, {"versioned_ensembl_gene_id":"ENSG00000053770.11","gene_symbol":"AP5M1","gene_name":"adaptor related protein complex 5 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:20192]","synonyms":"MUDENG,MuD,mu5,FLJ10813,C14orf108","biotype":"protein_coding","ncbi_id":"55745","summary":null,"start":57268909,"end":57298742,"strand":1,"description":"adaptor related protein complex 5 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:20192]"}, {"versioned_ensembl_gene_id":"ENSG00000267790.1","gene_symbol":"LINC01987","gene_name":"long intergenic non-protein coding RNA 1987 [Source:HGNC Symbol;Acc:HGNC:52819]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132174","summary":null,"start":77722872,"end":77728559,"strand":-1,"description":"long intergenic non-protein coding RNA 1987 [Source:HGNC Symbol;Acc:HGNC:52819]"}, {"versioned_ensembl_gene_id":"ENSG00000183514.4","gene_symbol":"TDGF1P2","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11702]","synonyms":"TDGF2,CRIPTO-2,CR-2","biotype":"processed_pseudogene","ncbi_id":"22816","summary":null,"start":227870083,"end":227870644,"strand":-1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11702]"}, {"versioned_ensembl_gene_id":"ENSG00000167414.4","gene_symbol":"GNG8","gene_name":"G protein subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:19664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94235","summary":null,"start":46634076,"end":46634685,"strand":-1,"description":"G protein subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:19664]"}, {"versioned_ensembl_gene_id":"ENSG00000213087.3","gene_symbol":"AL356535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151225550,"end":151225947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181027.10","gene_symbol":"FKRP","gene_name":"fukutin related protein [Source:HGNC Symbol;Acc:HGNC:17997]","synonyms":"MDC1C,LGMD2I","biotype":"protein_coding","ncbi_id":"79147","summary":"This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, cognitive disability, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2008]","start":46746046,"end":46776988,"strand":1,"description":"fukutin related protein [Source:HGNC Symbol;Acc:HGNC:17997]"}, {"versioned_ensembl_gene_id":"ENSG00000265121.1","gene_symbol":"AC068594.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77264180,"end":77264776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263718.2","gene_symbol":"AC068594.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77257737,"end":77281897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231291.3","gene_symbol":"AC106799.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4512262,"end":4516776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162344.3","gene_symbol":"FGF19","gene_name":"fibroblast growth factor 19 [Source:HGNC Symbol;Acc:HGNC:3675]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9965","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This growth factor is a high affinity, heparin dependent ligand for FGFR4. Expression of this gene was detected only in fetal but not adult brain tissue. Synergistic interaction of the chick homolog and Wnt-8c has been shown to be required for initiation of inner ear development. [provided by RefSeq, Jul 2008]","start":69698232,"end":69704642,"strand":-1,"description":"fibroblast growth factor 19 [Source:HGNC Symbol;Acc:HGNC:3675]"}, {"versioned_ensembl_gene_id":"ENSG00000234460.1","gene_symbol":"AL772337.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87864166,"end":87866290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227924.2","gene_symbol":"RBPJP6","gene_name":"RBPJ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643198","summary":null,"start":42497704,"end":42499134,"strand":-1,"description":"RBPJ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37486]"}, {"versioned_ensembl_gene_id":"ENSG00000248118.1","gene_symbol":"LINC01019","gene_name":"long intergenic non-protein coding RNA 1019 [Source:HGNC Symbol;Acc:HGNC:27742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285577","summary":null,"start":3417152,"end":3536094,"strand":-1,"description":"long intergenic non-protein coding RNA 1019 [Source:HGNC Symbol;Acc:HGNC:27742]"}, {"versioned_ensembl_gene_id":"ENSG00000249830.1","gene_symbol":"LINC02162","gene_name":"long intergenic non-protein coding RNA 2162 [Source:HGNC Symbol;Acc:HGNC:53023]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374624","summary":null,"start":3452816,"end":3461660,"strand":1,"description":"long intergenic non-protein coding RNA 2162 [Source:HGNC Symbol;Acc:HGNC:53023]"}, {"versioned_ensembl_gene_id":"ENSG00000064201.15","gene_symbol":"TSPAN32","gene_name":"tetraspanin 32 [Source:HGNC Symbol;Acc:HGNC:13410]","synonyms":"TSSC6,PHEMX","biotype":"protein_coding","ncbi_id":"10077","summary":"This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":2301997,"end":2318200,"strand":1,"description":"tetraspanin 32 [Source:HGNC Symbol;Acc:HGNC:13410]"}, {"versioned_ensembl_gene_id":"ENSG00000258758.1","gene_symbol":"AL137100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57040885,"end":57042504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198892.6","gene_symbol":"SHISA4","gene_name":"shisa family member 4 [Source:HGNC Symbol;Acc:HGNC:27139]","synonyms":"TMEM58,hShisa4,C1orf40","biotype":"protein_coding","ncbi_id":"149345","summary":null,"start":201888680,"end":201892306,"strand":1,"description":"shisa family member 4 [Source:HGNC Symbol;Acc:HGNC:27139]"}, {"versioned_ensembl_gene_id":"ENSG00000131473.16","gene_symbol":"ACLY","gene_name":"ATP citrate lyase [Source:HGNC Symbol;Acc:HGNC:115]","synonyms":"CLATP,ATPCL,ACL","biotype":"protein_coding","ncbi_id":"47","summary":"ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Dec 2014]","start":41866908,"end":41930542,"strand":-1,"description":"ATP citrate lyase [Source:HGNC Symbol;Acc:HGNC:115]"}, {"versioned_ensembl_gene_id":"ENSG00000203709.11","gene_symbol":"C1orf132","gene_name":"chromosome 1 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:32018]","synonyms":"FLJ35650","biotype":"lincRNA","ncbi_id":"100128537","summary":null,"start":207801518,"end":207879096,"strand":-1,"description":"chromosome 1 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:32018]"}, {"versioned_ensembl_gene_id":"ENSG00000227463.2","gene_symbol":"AL390838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84063443,"end":84094577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240611.1","gene_symbol":"AC010307.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133172218,"end":133173053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280104.1","gene_symbol":"AC010608.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133457805,"end":133458331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275649.1","gene_symbol":"AL445584.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42231811,"end":42354454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258996.2","gene_symbol":"AL359219.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59181593,"end":59181940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281560.1","gene_symbol":"LSINCT5","gene_name":"long stress-induced non-coding transcript 5 [Source:NCBI gene;Acc:101234261]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101234261","summary":null,"start":2712591,"end":2715237,"strand":1,"description":"long stress-induced non-coding transcript 5 [Source:NCBI gene;Acc:101234261]"}, {"versioned_ensembl_gene_id":"ENSG00000149716.12","gene_symbol":"ORAOV1","gene_name":"oral cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:17589]","synonyms":"TAOS1","biotype":"protein_coding","ncbi_id":"220064","summary":null,"start":69653076,"end":69675416,"strand":-1,"description":"oral cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:17589]"}, {"versioned_ensembl_gene_id":"ENSG00000275733.1","gene_symbol":"AC092266.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2261859,"end":2262023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155329.11","gene_symbol":"ZCCHC10","gene_name":"zinc finger CCHC-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25954]","synonyms":"FLJ20094","biotype":"protein_coding","ncbi_id":"54819","summary":null,"start":132996985,"end":133026604,"strand":-1,"description":"zinc finger CCHC-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25954]"}, {"versioned_ensembl_gene_id":"ENSG00000235183.3","gene_symbol":"AC015795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49795343,"end":49795669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236709.1","gene_symbol":"DAPK1-IT1","gene_name":"DAPK1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43591]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506897","summary":null,"start":87553454,"end":87554459,"strand":1,"description":"DAPK1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43591]"}, {"versioned_ensembl_gene_id":"ENSG00000250402.2","gene_symbol":"AC109471.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125376828,"end":125377439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258529.5","gene_symbol":"AP001781.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":111786286,"end":111879425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137720.7","gene_symbol":"C11orf1","gene_name":"chromosome 11 open reading frame 1 [Source:HGNC Symbol;Acc:HGNC:1163]","synonyms":"FLJ23499","biotype":"protein_coding","ncbi_id":"64776","summary":null,"start":111878935,"end":111885975,"strand":1,"description":"chromosome 11 open reading frame 1 [Source:HGNC Symbol;Acc:HGNC:1163]"}, {"versioned_ensembl_gene_id":"ENSG00000267344.1","gene_symbol":"AC003070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45396932,"end":45397477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167840.13","gene_symbol":"ZNF232","gene_name":"zinc finger protein 232 [Source:HGNC Symbol;Acc:HGNC:13026]","synonyms":"ZSCAN11","biotype":"protein_coding","ncbi_id":"7775","summary":null,"start":5105541,"end":5123116,"strand":-1,"description":"zinc finger protein 232 [Source:HGNC Symbol;Acc:HGNC:13026]"}, {"versioned_ensembl_gene_id":"ENSG00000254552.1","gene_symbol":"XIRP2-AS1","gene_name":"XIRP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40679]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874011","summary":null,"start":167123904,"end":167140955,"strand":-1,"description":"XIRP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40679]"}, {"versioned_ensembl_gene_id":"ENSG00000259109.1","gene_symbol":"AC004858.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73189763,"end":73190004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249112.1","gene_symbol":"AC112196.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124707827,"end":124710737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240355.1","gene_symbol":"AC004869.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46476457,"end":46477940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159593.14","gene_symbol":"NAE1","gene_name":"NEDD8 activating enzyme E1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:621]","synonyms":"APPBP1,APP-BP1,ula-1","biotype":"protein_coding","ncbi_id":"8883","summary":"The protein encoded by this gene binds to the beta-amyloid precursor protein. Beta-amyloid precursor protein is a cell surface protein with signal-transducing properties, and it is thought to play a role in the pathogenesis of Alzheimer's disease. In addition, the encoded protein can form a heterodimer with UBE1C and bind and activate NEDD8, a ubiquitin-like protein. This protein is required for cell cycle progression through the S/M checkpoint. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":66802875,"end":66873256,"strand":-1,"description":"NEDD8 activating enzyme E1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:621]"}, {"versioned_ensembl_gene_id":"ENSG00000250411.1","gene_symbol":"AC109458.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125036831,"end":125042239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145494.11","gene_symbol":"NDUFS6","gene_name":"NADH:ubiquinone oxidoreductase subunit S6 [Source:HGNC Symbol;Acc:HGNC:7713]","synonyms":"CI-13kA","biotype":"protein_coding","ncbi_id":"4726","summary":"This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009]","start":1801400,"end":1816605,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S6 [Source:HGNC Symbol;Acc:HGNC:7713]"}, {"versioned_ensembl_gene_id":"ENSG00000139946.9","gene_symbol":"PELI2","gene_name":"pellino E3 ubiquitin protein ligase family member 2 [Source:HGNC Symbol;Acc:HGNC:8828]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57161","summary":null,"start":56117814,"end":56301526,"strand":1,"description":"pellino E3 ubiquitin protein ligase family member 2 [Source:HGNC Symbol;Acc:HGNC:8828]"}, {"versioned_ensembl_gene_id":"ENSG00000134627.11","gene_symbol":"PIWIL4","gene_name":"piwi like RNA-mediated gene silencing 4 [Source:HGNC Symbol;Acc:HGNC:18444]","synonyms":"Miwi2,HIWI2,FLJ36156","biotype":"protein_coding","ncbi_id":"143689","summary":"PIWIL4 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003 [PubMed 12906857]).[supplied by OMIM, Mar 2008]","start":94543840,"end":94621421,"strand":1,"description":"piwi like RNA-mediated gene silencing 4 [Source:HGNC Symbol;Acc:HGNC:18444]"}, {"versioned_ensembl_gene_id":"ENSG00000277763.1","gene_symbol":"AL138995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56117316,"end":56117990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262456.1","gene_symbol":"AC006435.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2384847,"end":2386664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159314.11","gene_symbol":"ARHGAP27","gene_name":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]","synonyms":"SH3P20,SH3D20,FLJ43547,CAMGAP1","biotype":"protein_coding","ncbi_id":"201176","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may pay a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2013]","start":45393902,"end":45434421,"strand":-1,"description":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]"}, {"versioned_ensembl_gene_id":"ENSG00000255929.5","gene_symbol":"AP000943.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94545330,"end":94740355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254226.5","gene_symbol":"LINC01933","gene_name":"long intergenic non-protein coding RNA 1933 [Source:HGNC Symbol;Acc:HGNC:52756]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927115","summary":null,"start":151949571,"end":152270448,"strand":1,"description":"long intergenic non-protein coding RNA 1933 [Source:HGNC Symbol;Acc:HGNC:52756]"}, {"versioned_ensembl_gene_id":"ENSG00000089916.17","gene_symbol":"GPATCH2L","gene_name":"G-patch domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:20210]","synonyms":"FLJ20689,FLJ10033,C14orf118","biotype":"protein_coding","ncbi_id":"55668","summary":null,"start":76151916,"end":76254342,"strand":1,"description":"G-patch domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:20210]"}, {"versioned_ensembl_gene_id":"ENSG00000261987.2","gene_symbol":"KYNUP1","gene_name":"kynureninase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39199]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729321","summary":null,"start":19166896,"end":19169668,"strand":-1,"description":"kynureninase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39199]"}, {"versioned_ensembl_gene_id":"ENSG00000224650.2","gene_symbol":"IGHV3-74","gene_name":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28408","summary":null,"start":106810442,"end":106811131,"strand":-1,"description":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]"}, {"versioned_ensembl_gene_id":"ENSG00000249295.1","gene_symbol":"AC145146.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69477472,"end":69502466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223392.1","gene_symbol":"CLDN10-AS1","gene_name":"CLDN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39907]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874194","summary":null,"start":95479444,"end":95533910,"strand":-1,"description":"CLDN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39907]"}, {"versioned_ensembl_gene_id":"ENSG00000270978.1","gene_symbol":"AC091982.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151848886,"end":151850791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108861.8","gene_symbol":"DUSP3","gene_name":"dual specificity phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3069]","synonyms":"VHR","biotype":"protein_coding","ncbi_id":"1845","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene maps in a region that contains the BRCA1 locus which confers susceptibility to breast and ovarian cancer. Although DUSP3 is expressed in both breast and ovarian tissues, mutation screening in breast cancer pedigrees and in sporadic tumors was negative, leading to the conclusion that this gene is not BRCA1. [provided by RefSeq, Jul 2008]","start":43766121,"end":43778988,"strand":-1,"description":"dual specificity phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3069]"}, {"versioned_ensembl_gene_id":"ENSG00000282600.2","gene_symbol":"AC245369.7","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106728163,"end":106728615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275946.5","gene_symbol":"GU182345.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771241,"end":54780725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130005.12","gene_symbol":"GAMT","gene_name":"guanidinoacetate N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4136]","synonyms":"TP53I2,PIG2","biotype":"protein_coding","ncbi_id":"2593","summary":"The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene. Pseudogenes of this gene are found on chromosomes 2 and 13. [provided by RefSeq, Feb 2012]","start":1397026,"end":1401570,"strand":-1,"description":"guanidinoacetate N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4136]"}, {"versioned_ensembl_gene_id":"ENSG00000149591.16","gene_symbol":"TAGLN","gene_name":"transgelin [Source:HGNC Symbol;Acc:HGNC:11553]","synonyms":"WS3-10,TAGLN1,SMCC,SM22,DKFZp686P11128","biotype":"protein_coding","ncbi_id":"6876","summary":"This gene encodes a shape change and transformation sensitive actin-binding protein which belongs to the calponin family. It is ubiquitously expressed in vascular and visceral smooth muscle, and is an early marker of smooth muscle differentiation. The encoded protein is thought to be involved in calcium-independent smooth muscle contraction. It acts as a tumor suppressor, and the loss of its expression is an early event in cell transformation and the development of some tumors, coinciding with cellular plasticity. The encoded protein has a domain architecture consisting of an N-terminal calponin homology (CH) domain and a C-terminal calponin-like (CLIK) domain. Mice with a knockout of the orthologous gene are viable and fertile but their vascular smooth muscle cells exhibit alterations in the distribution of the actin filament and changes in cytoskeletal organization. [provided by RefSeq, Aug 2017]","start":117199321,"end":117204782,"strand":1,"description":"transgelin [Source:HGNC Symbol;Acc:HGNC:11553]"}, {"versioned_ensembl_gene_id":"ENSG00000172543.7","gene_symbol":"CTSW","gene_name":"cathepsin W [Source:HGNC Symbol;Acc:HGNC:2546]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1521","summary":"The protein encoded by this gene, a member of the peptidase C1 family, is a cysteine proteinase that may have a specific function in the mechanism or regulation of T-cell cytolytic activity. The encoded protein is found associated with the membrane inside the endoplasmic reticulum of natural killer and cytotoxic T-cells. Expression of this gene is up-regulated by interleukin-2. [provided by RefSeq, Jul 2008]","start":65879809,"end":65883741,"strand":1,"description":"cathepsin W [Source:HGNC Symbol;Acc:HGNC:2546]"}, {"versioned_ensembl_gene_id":"ENSG00000273535.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54836140,"end":54846123,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000145681.10","gene_symbol":"HAPLN1","gene_name":"hyaluronan and proteoglycan link protein 1 [Source:HGNC Symbol;Acc:HGNC:2380]","synonyms":"CRTL1","biotype":"protein_coding","ncbi_id":"1404","summary":null,"start":83637805,"end":83721613,"strand":-1,"description":"hyaluronan and proteoglycan link protein 1 [Source:HGNC Symbol;Acc:HGNC:2380]"}, {"versioned_ensembl_gene_id":"ENSG00000232579.1","gene_symbol":"MTCO1P27","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52092]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075168","summary":null,"start":12504665,"end":12504890,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52092]"}, {"versioned_ensembl_gene_id":"ENSG00000233603.1","gene_symbol":"JTBP1","gene_name":"jumping translocation breakpoint pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39180]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874254","summary":null,"start":40798039,"end":40798285,"strand":1,"description":"jumping translocation breakpoint pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39180]"}, {"versioned_ensembl_gene_id":"ENSG00000270038.1","gene_symbol":"AL133467.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95644508,"end":95645232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141576.14","gene_symbol":"RNF157","gene_name":"ring finger protein 157 [Source:HGNC Symbol;Acc:HGNC:29402]","synonyms":"KIAA1917","biotype":"protein_coding","ncbi_id":"114804","summary":null,"start":76142453,"end":76240373,"strand":-1,"description":"ring finger protein 157 [Source:HGNC Symbol;Acc:HGNC:29402]"}, {"versioned_ensembl_gene_id":"ENSG00000279485.1","gene_symbol":"AC016734.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":63517892,"end":63519268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275239.4","gene_symbol":"AL591926.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41657708,"end":41699072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137504.13","gene_symbol":"CREBZF","gene_name":"CREB/ATF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:24905]","synonyms":"ZF","biotype":"protein_coding","ncbi_id":"58487","summary":null,"start":85659708,"end":85682908,"strand":-1,"description":"CREB/ATF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:24905]"}, {"versioned_ensembl_gene_id":"ENSG00000269266.1","gene_symbol":"DNAJC19P2","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861445","summary":null,"start":41605341,"end":41605671,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]"}, {"versioned_ensembl_gene_id":"ENSG00000235121.1","gene_symbol":"AL645504.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201723294,"end":201737506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125257.13","gene_symbol":"ABCC4","gene_name":"ATP binding cassette subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:55]","synonyms":"EST170205,MRP4,MOATB,MOAT-B","biotype":"protein_coding","ncbi_id":"10257","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This family member plays a role in cellular detoxification as a pump for its substrate, organic anions. It may also function in prostaglandin-mediated cAMP signaling in ciliogenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":95019829,"end":95301446,"strand":-1,"description":"ATP binding cassette subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:55]"}, {"versioned_ensembl_gene_id":"ENSG00000250584.2","gene_symbol":"LINC01511","gene_name":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]","synonyms":"RP11-325I22.2","biotype":"lincRNA","ncbi_id":"100506791","summary":null,"start":1363582,"end":1380067,"strand":-1,"description":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]"}, {"versioned_ensembl_gene_id":"ENSG00000270147.1","gene_symbol":"AC068620.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56396312,"end":56396871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236390.1","gene_symbol":"AC092800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201673105,"end":201674144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112742.9","gene_symbol":"TTK","gene_name":"TTK protein kinase [Source:HGNC Symbol;Acc:HGNC:12401]","synonyms":"MPS1L1,MPS1,MPH1,CT96","biotype":"protein_coding","ncbi_id":"7272","summary":"This gene encodes a dual specificity protein kinase with the ability to phosphorylate tyrosine, serine and threonine. Associated with cell proliferation, this protein is essential for chromosome alignment at the centromere during mitosis and is required for centrosome duplication. It has been found to be a critical mitotic checkpoint protein for accurate segregation of chromosomes during mitosis. Tumorigenesis may occur when this protein fails to degrade and produces excess centrosomes resulting in aberrant mitotic spindles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":80003887,"end":80042527,"strand":1,"description":"TTK protein kinase [Source:HGNC Symbol;Acc:HGNC:12401]"}, {"versioned_ensembl_gene_id":"ENSG00000186564.5","gene_symbol":"FOXD2","gene_name":"forkhead box D2 [Source:HGNC Symbol;Acc:HGNC:3803]","synonyms":"FREAC9,FKHL17","biotype":"protein_coding","ncbi_id":"2306","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined. [provided by RefSeq, Jul 2008]","start":47436017,"end":47440691,"strand":1,"description":"forkhead box D2 [Source:HGNC Symbol;Acc:HGNC:3803]"}, {"versioned_ensembl_gene_id":"ENSG00000277718.1","gene_symbol":"LINC02255","gene_name":"long intergenic non-protein coding RNA 2255 [Source:HGNC Symbol;Acc:HGNC:53153]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370894","summary":null,"start":74379083,"end":74390535,"strand":1,"description":"long intergenic non-protein coding RNA 2255 [Source:HGNC Symbol;Acc:HGNC:53153]"}, {"versioned_ensembl_gene_id":"ENSG00000238230.1","gene_symbol":"LINC00391","gene_name":"long intergenic non-protein coding RNA 391 [Source:HGNC Symbol;Acc:HGNC:42719]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874154","summary":null,"start":94699694,"end":94702862,"strand":-1,"description":"long intergenic non-protein coding RNA 391 [Source:HGNC Symbol;Acc:HGNC:42719]"}, {"versioned_ensembl_gene_id":"ENSG00000248268.1","gene_symbol":"AC010275.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111277517,"end":111302567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225762.1","gene_symbol":"LINC01389","gene_name":"long intergenic non-protein coding RNA 1389 [Source:HGNC Symbol;Acc:HGNC:50661]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724077","summary":null,"start":47380928,"end":47408477,"strand":-1,"description":"long intergenic non-protein coding RNA 1389 [Source:HGNC Symbol;Acc:HGNC:50661]"}, {"versioned_ensembl_gene_id":"ENSG00000113140.10","gene_symbol":"SPARC","gene_name":"secreted protein acidic and cysteine rich [Source:HGNC Symbol;Acc:HGNC:11219]","synonyms":"ON","biotype":"protein_coding","ncbi_id":"6678","summary":"This gene encodes a cysteine-rich acidic matrix-associated protein. The encoded protein is required for the collagen in bone to become calcified but is also involved in extracellular matrix synthesis and promotion of changes to cell shape. The gene product has been associated with tumor suppression but has also been correlated with metastasis based on changes to cell shape which can promote tumor cell invasion. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2015]","start":151661096,"end":151687165,"strand":-1,"description":"secreted protein acidic and cysteine rich [Source:HGNC Symbol;Acc:HGNC:11219]"}, {"versioned_ensembl_gene_id":"ENSG00000176907.4","gene_symbol":"C8orf4","gene_name":"chromosome 8 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1357]","synonyms":"TC1,TC-1,hTC-1","biotype":"protein_coding","ncbi_id":"56892","summary":"This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/beta-catenin signaling pathway. This protein interacts with a repressor of beta-catenin mediated transcription at nuclear speckles. It is thought to competitively block interactions of the repressor with beta-catenin, resulting in up-regulation of beta-catenin target genes. The encoded protein may also play a role in the NF-kappaB and ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, breast cancer and hematological malignancies. [provided by RefSeq, Nov 2011]","start":40153455,"end":40155308,"strand":1,"description":"chromosome 8 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1357]"}, {"versioned_ensembl_gene_id":"ENSG00000255485.1","gene_symbol":"OR5G4P","gene_name":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81192","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56790206,"end":56790965,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]"}, {"versioned_ensembl_gene_id":"ENSG00000160014.16","gene_symbol":"CALM3","gene_name":"calmodulin 3 [Source:HGNC Symbol;Acc:HGNC:1449]","synonyms":"PHKD","biotype":"protein_coding","ncbi_id":"808","summary":"This gene encodes a member of a family of proteins that binds calcium and functions as a enzymatic co-factor. Activity of this protein is important in the regulation of the cell cycle and cytokinesis. Multiple alternatively spliced transcript variants have been observed at this gene. [provided by RefSeq, Aug 2016]","start":46601074,"end":46610793,"strand":1,"description":"calmodulin 3 [Source:HGNC Symbol;Acc:HGNC:1449]"}, {"versioned_ensembl_gene_id":"ENSG00000161533.11","gene_symbol":"ACOX1","gene_name":"acyl-CoA oxidase 1 [Source:HGNC Symbol;Acc:HGNC:119]","synonyms":"PALMCOX","biotype":"protein_coding","ncbi_id":"51","summary":"The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":75941507,"end":75979363,"strand":-1,"description":"acyl-CoA oxidase 1 [Source:HGNC Symbol;Acc:HGNC:119]"}, {"versioned_ensembl_gene_id":"ENSG00000147394.18","gene_symbol":"ZNF185","gene_name":"zinc finger protein 185 with LIM domain [Source:HGNC Symbol;Acc:HGNC:12976]","synonyms":"SCELL","biotype":"protein_coding","ncbi_id":"7739","summary":"Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a LIM-domain zinc finger protein. The LIM domain is composed of two contiguous zinc finger domains, separated by a two-amino acid residue hydrophobic linker. The LIM domain mediates protein:protein interactions. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010]","start":152914442,"end":152973480,"strand":1,"description":"zinc finger protein 185 with LIM domain [Source:HGNC Symbol;Acc:HGNC:12976]"}, {"versioned_ensembl_gene_id":"ENSG00000163898.9","gene_symbol":"LIPH","gene_name":"lipase H [Source:HGNC Symbol;Acc:HGNC:18483]","synonyms":"PLA1B,mPA-PLA1alpha,mPA-PLA1,LPDLR","biotype":"protein_coding","ncbi_id":"200879","summary":"This gene encodes a membrane-bound member of the mammalian triglyceride lipase family. It catalyzes the production of 2-acyl lysophosphatidic acid (LPA), which is a lipid mediator with diverse biological properties that include platelet aggregation, smooth muscle contraction, and stimulation of cell proliferation and motility. [provided by RefSeq, Jul 2008]","start":185506262,"end":185552613,"strand":-1,"description":"lipase H [Source:HGNC Symbol;Acc:HGNC:18483]"}, {"versioned_ensembl_gene_id":"ENSG00000257195.1","gene_symbol":"HNRNPA1P50","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728170","summary":null,"start":92883773,"end":92884700,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48780]"}, {"versioned_ensembl_gene_id":"ENSG00000183560.9","gene_symbol":"IZUMO1R","gene_name":"IZUMO1 receptor, JUNO [Source:HGNC Symbol;Acc:HGNC:32565]","synonyms":"JUNO,FOLR4,Folbp3","biotype":"protein_coding","ncbi_id":"390243","summary":null,"start":94305592,"end":94307721,"strand":1,"description":"IZUMO1 receptor, JUNO [Source:HGNC Symbol;Acc:HGNC:32565]"}, {"versioned_ensembl_gene_id":"ENSG00000239210.2","gene_symbol":"RPS26P55","gene_name":"ribosomal protein S26 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129650","summary":null,"start":34533427,"end":34534084,"strand":-1,"description":"ribosomal protein S26 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36500]"}, {"versioned_ensembl_gene_id":"ENSG00000253802.1","gene_symbol":"AC105999.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40298741,"end":40343402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169515.5","gene_symbol":"CCDC8","gene_name":"coiled-coil domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25367]","synonyms":"PPP1R20,DKFZp564K0322,3M3","biotype":"protein_coding","ncbi_id":"83987","summary":"This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1. Mutations in this gene are a cause of 3M syndrome-3 (3M3). [provided by RefSeq, Dec 2011]","start":46410372,"end":46413584,"strand":-1,"description":"coiled-coil domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25367]"}, {"versioned_ensembl_gene_id":"ENSG00000233164.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30691675,"end":30697740,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000213574.2","gene_symbol":"LDHAP5","gene_name":"lactate dehydrogenase A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:6540]","synonyms":"LDHAL5","biotype":"processed_pseudogene","ncbi_id":"729666","summary":null,"start":118932674,"end":118933295,"strand":-1,"description":"lactate dehydrogenase A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:6540]"}, {"versioned_ensembl_gene_id":"ENSG00000254326.1","gene_symbol":"IGHV7-27","gene_name":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28383","summary":null,"start":106317823,"end":106318236,"strand":-1,"description":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]"}, {"versioned_ensembl_gene_id":"ENSG00000238275.2","gene_symbol":"HOMER2P2","gene_name":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317769","summary":null,"start":106286811,"end":106287657,"strand":-1,"description":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]"}, {"versioned_ensembl_gene_id":"ENSG00000259143.1","gene_symbol":"AL356017.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":95185117,"end":95185854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240480.1","gene_symbol":"RPL29P2","gene_name":"ribosomal protein L29 pseudogene 2 [Source:NCBI gene;Acc:118432]","synonyms":"RPL29_10_1510","biotype":"transcribed_processed_pseudogene","ncbi_id":"118432","summary":null,"start":7754320,"end":7754976,"strand":1,"description":"ribosomal protein L29 pseudogene 2 [Source:NCBI gene;Acc:118432]"}, {"versioned_ensembl_gene_id":"ENSG00000280486.1","gene_symbol":"AC005329.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1386804,"end":1389651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172938.3","gene_symbol":"MRGPRD","gene_name":"MAS related GPR family member D [Source:HGNC Symbol;Acc:HGNC:29626]","synonyms":"mrgD","biotype":"protein_coding","ncbi_id":"116512","summary":null,"start":68980021,"end":68980986,"strand":-1,"description":"MAS related GPR family member D [Source:HGNC Symbol;Acc:HGNC:29626]"}, {"versioned_ensembl_gene_id":"ENSG00000136944.17","gene_symbol":"LMX1B","gene_name":"LIM homeobox transcription factor 1 beta [Source:HGNC Symbol;Acc:HGNC:6654]","synonyms":"NPS1","biotype":"protein_coding","ncbi_id":"4010","summary":"This gene encodes a member of LIM-homeodomain family of proteins containing two N-terminal zinc-binding LIM domains, 1 homeodomain, and a C-terminal glutamine-rich domain. It functions as a transcription factor, and is essential for the normal development of dorsal limb structures, the glomerular basement membrane, the anterior segment of the eye, and dopaminergic and serotonergic neurons. Mutations in this gene are associated with nail-patella syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":126614443,"end":126701032,"strand":1,"description":"LIM homeobox transcription factor 1 beta [Source:HGNC Symbol;Acc:HGNC:6654]"}, {"versioned_ensembl_gene_id":"ENSG00000238010.1","gene_symbol":"AL161908.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":126640756,"end":126641293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267801.1","gene_symbol":"AC087289.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75876372,"end":75879546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152760.9","gene_symbol":"TCTEX1D1","gene_name":"Tctex1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26882]","synonyms":"FLJ40873","biotype":"protein_coding","ncbi_id":"200132","summary":null,"start":66752459,"end":66778787,"strand":1,"description":"Tctex1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26882]"}, {"versioned_ensembl_gene_id":"ENSG00000143105.7","gene_symbol":"KCNA10","gene_name":"potassium voltage-gated channel subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:6219]","synonyms":"Kv1.8","biotype":"protein_coding","ncbi_id":"3744","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It is specifically regulated by cGMP and postulated to mediate the effects of substances that increase intracellular cGMP. This gene is intronless, and the gene is clustered with genes KCNA2 and KCNA3 on chromosome 1. [provided by RefSeq, Jul 2008]","start":110517217,"end":110519175,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:6219]"}, {"versioned_ensembl_gene_id":"ENSG00000232725.1","gene_symbol":"U52111.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153735626,"end":153766478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110777.11","gene_symbol":"POU2AF1","gene_name":"POU class 2 associating factor 1 [Source:HGNC Symbol;Acc:HGNC:9211]","synonyms":"OBF1,BOB1","biotype":"protein_coding","ncbi_id":"5450","summary":null,"start":111352252,"end":111455630,"strand":-1,"description":"POU class 2 associating factor 1 [Source:HGNC Symbol;Acc:HGNC:9211]"}, {"versioned_ensembl_gene_id":"ENSG00000197863.8","gene_symbol":"ZNF790","gene_name":"zinc finger protein 790 [Source:HGNC Symbol;Acc:HGNC:33114]","synonyms":"MGC62100,FLJ20350","biotype":"protein_coding","ncbi_id":"388536","summary":null,"start":36817428,"end":36850787,"strand":-1,"description":"zinc finger protein 790 [Source:HGNC Symbol;Acc:HGNC:33114]"}, {"versioned_ensembl_gene_id":"ENSG00000275080.5","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54798381,"end":54812886,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000235407.1","gene_symbol":"CYMP-AS1","gene_name":"CYMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52509]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440602","summary":null,"start":110487680,"end":110490258,"strand":-1,"description":"CYMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52509]"}, {"versioned_ensembl_gene_id":"ENSG00000251247.10","gene_symbol":"ZNF345","gene_name":"zinc finger protein 345 [Source:HGNC Symbol;Acc:HGNC:16367]","synonyms":"HZF10","biotype":"protein_coding","ncbi_id":"25850","summary":null,"start":36850361,"end":36913029,"strand":1,"description":"zinc finger protein 345 [Source:HGNC Symbol;Acc:HGNC:16367]"}, {"versioned_ensembl_gene_id":"ENSG00000271419.1","gene_symbol":"AL035410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114353986,"end":114355178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273698.1","gene_symbol":"MRPL57P1","gene_name":"mitochondrial ribosomal protein L57 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29686]","synonyms":"MRP63P1","biotype":"processed_pseudogene","ncbi_id":"126581","summary":null,"start":114279011,"end":114279275,"strand":-1,"description":"mitochondrial ribosomal protein L57 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29686]"}, {"versioned_ensembl_gene_id":"ENSG00000226687.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529298,"end":29533446,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000234268.1","gene_symbol":"AP000936.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117035797,"end":117036051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254046.1","gene_symbol":"IGHV1-17","gene_name":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28469","summary":null,"start":106174342,"end":106174760,"strand":-1,"description":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]"}, {"versioned_ensembl_gene_id":"ENSG00000211944.2","gene_symbol":"IGHV3-16","gene_name":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28447","summary":null,"start":106165205,"end":106165730,"strand":-1,"description":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]"}, {"versioned_ensembl_gene_id":"ENSG00000266980.1","gene_symbol":"AC087289.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75818815,"end":75820055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132382.14","gene_symbol":"MYBBP1A","gene_name":"MYB binding protein 1a [Source:HGNC Symbol;Acc:HGNC:7546]","synonyms":"Pol5,PAP2,P160,FLJ37886","biotype":"protein_coding","ncbi_id":"10514","summary":"This gene encodes a nucleolar transcriptional regulator that was first identified by its ability to bind specifically to the Myb proto-oncogene protein. The encoded protein is thought to play a role in many cellular processes including response to nucleolar stress, tumor suppression and synthesis of ribosomal DNA. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":4538897,"end":4555631,"strand":-1,"description":"MYB binding protein 1a [Source:HGNC Symbol;Acc:HGNC:7546]"}, {"versioned_ensembl_gene_id":"ENSG00000229320.3","gene_symbol":"KRT8P12","gene_name":"keratin 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:28057]","synonyms":"KRT8L2","biotype":"transcribed_processed_pseudogene","ncbi_id":"90133","summary":null,"start":160565447,"end":160569248,"strand":1,"description":"keratin 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:28057]"}, {"versioned_ensembl_gene_id":"ENSG00000276085.1","gene_symbol":"CCL3L3","gene_name":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]","synonyms":"MGC12815","biotype":"protein_coding","ncbi_id":"414062","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this gene binds to several chemokine receptors, including chemokine binding protein 2 and chemokine (C-C motif) receptor 5 (CCR5). CCR5 is a co-receptor for HIV, and binding of this protein to CCR5 inhibits HIV entry. The copy number of this gene varies among individuals, where most individuals have one to six copies, and a minority of individuals have zero or more than six copies. There are conflicting reports about copy number variation of this gene and its correlation to disease susceptibility.[provided by RefSeq, Apr 2014]","start":36194869,"end":36196758,"strand":-1,"description":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]"}, {"versioned_ensembl_gene_id":"ENSG00000274767.1","gene_symbol":"AC243829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36183235,"end":36196471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255520.1","gene_symbol":"AC090589.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47123104,"end":47130801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270190.1","gene_symbol":"AC068491.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111266868,"end":111267473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263020.6","gene_symbol":"AL662899.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31666102,"end":31673546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237043.1","gene_symbol":"AL929561.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026665,"end":29027592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226706.1","gene_symbol":"AL161452.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135503273,"end":135506447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125945.14","gene_symbol":"ZNF436","gene_name":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]","synonyms":"Zfp46,KIAA1710","biotype":"protein_coding","ncbi_id":"80818","summary":null,"start":23359448,"end":23369442,"strand":-1,"description":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]"}, {"versioned_ensembl_gene_id":"ENSG00000245750.7","gene_symbol":"DRAIC","gene_name":"downregulated RNA in cancer, inhibitor of cell invasion and migration [Source:HGNC Symbol;Acc:HGNC:27082]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145837","summary":null,"start":69463026,"end":69571440,"strand":1,"description":"downregulated RNA in cancer, inhibitor of cell invasion and migration [Source:HGNC Symbol;Acc:HGNC:27082]"}, {"versioned_ensembl_gene_id":"ENSG00000275659.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,CD158e1/2,nkat3,NKB1,CD158e2,NKB1B,cl-11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814901,"end":54878560,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000241680.1","gene_symbol":"AC002350.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110460988,"end":110461362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279650.1","gene_symbol":"AC073912.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130775694,"end":130776546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270580.5","gene_symbol":"PKD1P6-NPIPP1","gene_name":"PKD1P6-NPIPP1 readthrough [Source:NCBI gene;Acc:105369154]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"105369154","summary":"This locus represents naturally-occurring readthrough transcription between two unprocessed pseudogenes, PKD1P6 (polycystic kidney disease 1 (autosomal dominant) pseudogene 6) and NPIPP1 (nuclear pore complex interacting protein pseudogene 1). The individual pseudogene loci are not curated as transcribed regions. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Jan 2016]","start":15104723,"end":15131601,"strand":-1,"description":"PKD1P6-NPIPP1 readthrough [Source:NCBI gene;Acc:105369154]"}, {"versioned_ensembl_gene_id":"ENSG00000221932.6","gene_symbol":"HEPN1","gene_name":"hepatocellular carcinoma, down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:34400]","synonyms":null,"biotype":"protein_coding","ncbi_id":"641654","summary":"This gene is expressed predominantly in the liver. Transient transfection studies show the expression of this gene significantly inhibits cell growth, suggesting a role for this gene in apoptosis. Expression of this gene is down-regulated or lost in hepatocellular carcinomas (HCC), suggesting that loss of this gene is involved in carcinogenesis of hepatocytes (PMID:12971969). This gene maps to the 3'-noncoding region of the HEPACAM gene (GeneID:220296) on the antisense strand. [provided by RefSeq, Aug 2020]","start":124919244,"end":124920677,"strand":1,"description":"hepatocellular carcinoma, down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:34400]"}, {"versioned_ensembl_gene_id":"ENSG00000240801.1","gene_symbol":"AC132217.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":2129121,"end":2129964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280890.1","gene_symbol":"AC073324.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55235965,"end":55255635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167244.18","gene_symbol":"IGF2","gene_name":"insulin like growth factor 2 [Source:HGNC Symbol;Acc:HGNC:5466]","synonyms":"IGF-II,FLJ44734,C11orf43","biotype":"protein_coding","ncbi_id":"3481","summary":"This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":2129112,"end":2141238,"strand":-1,"description":"insulin like growth factor 2 [Source:HGNC Symbol;Acc:HGNC:5466]"}, {"versioned_ensembl_gene_id":"ENSG00000237781.3","gene_symbol":"AL356356.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150548562,"end":150557724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168872.16","gene_symbol":"DDX19A","gene_name":"DEAD-box helicase 19A [Source:HGNC Symbol;Acc:HGNC:25628]","synonyms":"FLJ11126,DDX19L","biotype":"protein_coding","ncbi_id":"55308","summary":null,"start":70346829,"end":70373383,"strand":1,"description":"DEAD-box helicase 19A [Source:HGNC Symbol;Acc:HGNC:25628]"}, {"versioned_ensembl_gene_id":"ENSG00000105821.14","gene_symbol":"DNAJC2","gene_name":"DnaJ heat shock protein family (Hsp40) member C2 [Source:HGNC Symbol;Acc:HGNC:13192]","synonyms":"zuotin,ZUO1,ZRF1,MPP11,MPHOSPH11","biotype":"protein_coding","ncbi_id":"27000","summary":"This gene is a member of the M-phase phosphoprotein (MPP) family. The gene encodes a phosphoprotein with a J domain and a Myb DNA-binding domain which localizes to both the nucleus and the cytosol. The protein is capable of forming a heterodimeric complex that associates with ribosomes, acting as a molecular chaperone for nascent polypeptide chains as they exit the ribosome. This protein was identified as a leukemia-associated antigen and expression of the gene is upregulated in leukemic blasts. Also, chromosomal aberrations involving this gene are associated with primary head and neck squamous cell tumors. This gene has a pseudogene on chromosome 6. Alternatively spliced variants which encode different protein isoforms have been described. [provided by RefSeq, Jul 2008]","start":103312474,"end":103344873,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C2 [Source:HGNC Symbol;Acc:HGNC:13192]"}, {"versioned_ensembl_gene_id":"ENSG00000186026.6","gene_symbol":"ZNF284","gene_name":"zinc finger protein 284 [Source:HGNC Symbol;Acc:HGNC:13078]","synonyms":"DKFZp781F1775","biotype":"protein_coding","ncbi_id":"342909","summary":null,"start":44072144,"end":44089613,"strand":1,"description":"zinc finger protein 284 [Source:HGNC Symbol;Acc:HGNC:13078]"}, {"versioned_ensembl_gene_id":"ENSG00000241069.1","gene_symbol":"AC125388.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53386233,"end":53386388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159885.13","gene_symbol":"ZNF222","gene_name":"zinc finger protein 222 [Source:HGNC Symbol;Acc:HGNC:13015]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7673","summary":null,"start":44025342,"end":44033112,"strand":1,"description":"zinc finger protein 222 [Source:HGNC Symbol;Acc:HGNC:13015]"}, {"versioned_ensembl_gene_id":"ENSG00000160183.13","gene_symbol":"TMPRSS3","gene_name":"transmembrane protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:11877]","synonyms":"DFNB8,DFNB10","biotype":"protein_coding","ncbi_id":"64699","summary":"This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor-associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":42371890,"end":42396846,"strand":-1,"description":"transmembrane protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:11877]"}, {"versioned_ensembl_gene_id":"ENSG00000269758.1","gene_symbol":"AC092070.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53267870,"end":53270932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255372.1","gene_symbol":"AC107886.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22261209,"end":22262256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253332.1","gene_symbol":"AP005902.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39860219,"end":39860525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253755.1","gene_symbol":"IGHGP","gene_name":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]","synonyms":"IGHGP1","biotype":"IG_C_pseudogene","ncbi_id":"3505","summary":null,"start":105664633,"end":105669843,"strand":-1,"description":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]"}, {"versioned_ensembl_gene_id":"ENSG00000197928.10","gene_symbol":"ZNF677","gene_name":"zinc finger protein 677 [Source:HGNC Symbol;Acc:HGNC:28730]","synonyms":"MGC48625","biotype":"protein_coding","ncbi_id":"342926","summary":null,"start":53235381,"end":53254898,"strand":-1,"description":"zinc finger protein 677 [Source:HGNC Symbol;Acc:HGNC:28730]"}, {"versioned_ensembl_gene_id":"ENSG00000231049.2","gene_symbol":"OR52B5P","gene_name":"olfactory receptor family 52 subfamily B member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15210]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81270","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5557096,"end":5564327,"strand":1,"description":"olfactory receptor family 52 subfamily B member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15210]"}, {"versioned_ensembl_gene_id":"ENSG00000197728.9","gene_symbol":"RPS26","gene_name":"ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:10414]","synonyms":"S26","biotype":"protein_coding","ncbi_id":"6231","summary":"This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S26E family of ribosomal proteins. Mutations in this gene are found in Diamond-Blackfan anemia 10. There are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Aug 2017]","start":56041853,"end":56044675,"strand":1,"description":"ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:10414]"}, {"versioned_ensembl_gene_id":"ENSG00000234952.1","gene_symbol":"AL139121.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117735313,"end":117736407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165416.14","gene_symbol":"SUGT1","gene_name":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone [Source:HGNC Symbol;Acc:HGNC:16987]","synonyms":"SGT1","biotype":"protein_coding","ncbi_id":"10910","summary":"This gene encodes a highly conserved nuclear protein involved in kinetochore function and required for the G1/S and G2/M transitions. This protein interacts with heat shock protein 90. Alternative splicing results in multiple transcript variants. Pseudogenes for this gene have been defined on several different chromosomes. [provided by RefSeq, Mar 2016]","start":52652709,"end":52700909,"strand":1,"description":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone [Source:HGNC Symbol;Acc:HGNC:16987]"}, {"versioned_ensembl_gene_id":"ENSG00000163815.5","gene_symbol":"CLEC3B","gene_name":"C-type lectin domain family 3 member B [Source:HGNC Symbol;Acc:HGNC:11891]","synonyms":"TNA,TN","biotype":"protein_coding","ncbi_id":"7123","summary":null,"start":45001548,"end":45036071,"strand":1,"description":"C-type lectin domain family 3 member B [Source:HGNC Symbol;Acc:HGNC:11891]"}, {"versioned_ensembl_gene_id":"ENSG00000213401.9","gene_symbol":"MAGEA12","gene_name":"MAGE family member A12 [Source:HGNC Symbol;Acc:HGNC:6799]","synonyms":"MAGE12,CT1.12","biotype":"protein_coding","ncbi_id":"4111","summary":"This gene is closely related to several other genes clustered on chromosome X. These genes may be overexpressed in tumors. Multiple alternatively spliced variants encoding the same protein have been identified. [provided by RefSeq, Jun 2014]","start":152733779,"end":152737669,"strand":1,"description":"MAGE family member A12 [Source:HGNC Symbol;Acc:HGNC:6799]"}, {"versioned_ensembl_gene_id":"ENSG00000242599.7","gene_symbol":"CSAG4","gene_name":"CSAG family member 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20923]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100130935","summary":null,"start":152733827,"end":152740985,"strand":1,"description":"CSAG family member 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20923]"}, {"versioned_ensembl_gene_id":"ENSG00000226535.1","gene_symbol":"AL445487.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107169569,"end":107171148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230087.1","gene_symbol":"AC104389.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5354692,"end":5355578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225616.2","gene_symbol":"AL138785.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28982278,"end":28982608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272841.1","gene_symbol":"AL139393.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160990318,"end":160992342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259708.1","gene_symbol":"AC090607.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78250502,"end":78264156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160113.5","gene_symbol":"NR2F6","gene_name":"nuclear receptor subfamily 2 group F member 6 [Source:HGNC Symbol;Acc:HGNC:7977]","synonyms":"ERBAL2,EAR-2","biotype":"protein_coding","ncbi_id":"2063","summary":null,"start":17231883,"end":17245940,"strand":-1,"description":"nuclear receptor subfamily 2 group F member 6 [Source:HGNC Symbol;Acc:HGNC:7977]"}, {"versioned_ensembl_gene_id":"ENSG00000177885.13","gene_symbol":"GRB2","gene_name":"growth factor receptor bound protein 2 [Source:HGNC Symbol;Acc:HGNC:4566]","synonyms":"NCKAP2","biotype":"protein_coding","ncbi_id":"2885","summary":"The protein encoded by this gene binds the epidermal growth factor receptor and contains one SH2 domain and two SH3 domains. Its two SH3 domains direct complex formation with proline-rich regions of other proteins, and its SH2 domain binds tyrosine phosphorylated sequences. This gene is similar to the Sem5 gene of C.elegans, which is involved in the signal transduction pathway. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75318076,"end":75405709,"strand":-1,"description":"growth factor receptor bound protein 2 [Source:HGNC Symbol;Acc:HGNC:4566]"}, {"versioned_ensembl_gene_id":"ENSG00000267372.2","gene_symbol":"AC005330.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1321225,"end":1322846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229521.2","gene_symbol":"MYCBP2-AS2","gene_name":"MYCBP2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41024]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874213","summary":null,"start":77080511,"end":77081190,"strand":-1,"description":"MYCBP2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41024]"}, {"versioned_ensembl_gene_id":"ENSG00000280223.1","gene_symbol":"AL645820.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126004446,"end":126006118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176407.17","gene_symbol":"KCMF1","gene_name":"potassium channel modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:20589]","synonyms":"ZZZ1,PCMF,DKFZP434L1021,DEBT91","biotype":"protein_coding","ncbi_id":"56888","summary":null,"start":84971093,"end":85059472,"strand":1,"description":"potassium channel modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:20589]"}, {"versioned_ensembl_gene_id":"ENSG00000282815.1","gene_symbol":"TEX13C","gene_name":"TEX13 family member C [Source:HGNC Symbol;Acc:HGNC:52277]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129520","summary":null,"start":125320120,"end":125325214,"strand":1,"description":"TEX13 family member C [Source:HGNC Symbol;Acc:HGNC:52277]"}, {"versioned_ensembl_gene_id":"ENSG00000237062.1","gene_symbol":"AL512649.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106615078,"end":106615806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234323.6","gene_symbol":"LINC01505","gene_name":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]","synonyms":"RP11-308N19.1,RP11-308N19.1","biotype":"lincRNA","ncbi_id":"100996590","summary":null,"start":105993310,"end":106740875,"strand":1,"description":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]"}, {"versioned_ensembl_gene_id":"ENSG00000196876.15","gene_symbol":"SCN8A","gene_name":"sodium voltage-gated channel alpha subunit 8 [Source:HGNC Symbol;Acc:HGNC:10596]","synonyms":"PN4,Nav1.6,NaCh6,MED,CIAT,CerIII","biotype":"protein_coding","ncbi_id":"6334","summary":"This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with cognitive disability, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":51590266,"end":51812864,"strand":1,"description":"sodium voltage-gated channel alpha subunit 8 [Source:HGNC Symbol;Acc:HGNC:10596]"}, {"versioned_ensembl_gene_id":"ENSG00000165219.21","gene_symbol":"GAPVD1","gene_name":"GTPase activating protein and VPS9 domains 1 [Source:HGNC Symbol;Acc:HGNC:23375]","synonyms":"KIAA1521,DKFZP434C212","biotype":"protein_coding","ncbi_id":"26130","summary":null,"start":125261794,"end":125367207,"strand":1,"description":"GTPase activating protein and VPS9 domains 1 [Source:HGNC Symbol;Acc:HGNC:23375]"}, {"versioned_ensembl_gene_id":"ENSG00000146648.17","gene_symbol":"EGFR","gene_name":"epidermal growth factor receptor [Source:HGNC Symbol;Acc:HGNC:3236]","synonyms":"ERBB,ERBB1","biotype":"protein_coding","ncbi_id":"1956","summary":"The protein encoded by this gene is a transmembrane glycoprotein that is a member of the protein kinase superfamily. This protein is a receptor for members of the epidermal growth factor family. EGFR is a cell surface protein that binds to epidermal growth factor, thus inducing receptor dimerization and tyrosine autophosphorylation leading to cell proliferation. Mutations in this gene are associated with lung cancer. EGFR is a component of the cytokine storm which contributes to a severe form of Coronavirus Disease 2019 (COVID-19) resulting from infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). [provided by RefSeq, Jul 2020]","start":55019021,"end":55211628,"strand":1,"description":"epidermal growth factor receptor [Source:HGNC Symbol;Acc:HGNC:3236]"}, {"versioned_ensembl_gene_id":"ENSG00000265399.1","gene_symbol":"AP005329.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3190397,"end":3247277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126337.13","gene_symbol":"KRT36","gene_name":"keratin 36 [Source:HGNC Symbol;Acc:HGNC:6454]","synonyms":"KRTHA6","biotype":"protein_coding","ncbi_id":"8689","summary":"The protein encoded by this gene is a member of the keratin gene family. This type I hair keratin is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41486136,"end":41492546,"strand":-1,"description":"keratin 36 [Source:HGNC Symbol;Acc:HGNC:6454]"}, {"versioned_ensembl_gene_id":"ENSG00000235416.1","gene_symbol":"AC233728.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53456273,"end":53457029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233211.2","gene_symbol":"GRPEL2P1","gene_name":"GrpE like 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874360","summary":null,"start":88978447,"end":88978785,"strand":-1,"description":"GrpE like 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41969]"}, {"versioned_ensembl_gene_id":"ENSG00000216721.3","gene_symbol":"AC093850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":215804731,"end":215804981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280123.1","gene_symbol":"AC023632.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":94427712,"end":94429888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228618.1","gene_symbol":"AC012462.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215476667,"end":215480248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230695.1","gene_symbol":"AC012462.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":215436253,"end":215436992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244734.3","gene_symbol":"HBB","gene_name":"hemoglobin subunit beta [Source:HGNC Symbol;Acc:HGNC:4827]","synonyms":"HBD,CD113t-C,beta-globin","biotype":"protein_coding","ncbi_id":"3043","summary":"The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. The normal adult hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta-zero-thalassemia. Reduced amounts of detectable beta globin causes beta-plus-thalassemia. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]","start":5225464,"end":5229395,"strand":-1,"description":"hemoglobin subunit beta [Source:HGNC Symbol;Acc:HGNC:4827]"}, {"versioned_ensembl_gene_id":"ENSG00000126777.17","gene_symbol":"KTN1","gene_name":"kinectin 1 [Source:HGNC Symbol;Acc:HGNC:6467]","synonyms":"KNT,KIAA0004,CG1","biotype":"protein_coding","ncbi_id":"3895","summary":"This gene encodes an integral membrane protein that is a member of the kinectin protein family. The encoded protein is primarily localized to the endoplasmic reticulum membrane. This protein binds kinesin and may be involved in intracellular organelle motility. This protein also binds translation elongation factor-delta and may be involved in the assembly of the elongation factor-1 complex. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2012]","start":55559072,"end":55701526,"strand":1,"description":"kinectin 1 [Source:HGNC Symbol;Acc:HGNC:6467]"}, {"versioned_ensembl_gene_id":"ENSG00000034510.5","gene_symbol":"TMSB10","gene_name":"thymosin beta 10 [Source:HGNC Symbol;Acc:HGNC:11879]","synonyms":"TB10","biotype":"protein_coding","ncbi_id":"9168","summary":null,"start":84905625,"end":84906675,"strand":1,"description":"thymosin beta 10 [Source:HGNC Symbol;Acc:HGNC:11879]"}, {"versioned_ensembl_gene_id":"ENSG00000104783.11","gene_symbol":"KCNN4","gene_name":"potassium calcium-activated channel subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:6293]","synonyms":"KCa3.1,IK,hSK4,hKCa4,hIKCa1","biotype":"protein_coding","ncbi_id":"3783","summary":"The protein encoded by this gene is part of a potentially heterotetrameric voltage-independent potassium channel that is activated by intracellular calcium. Activation is followed by membrane hyperpolarization, which promotes calcium influx. The encoded protein may be part of the predominant calcium-activated potassium channel in T-lymphocytes. This gene is similar to other KCNN family potassium channel genes, but it differs enough to possibly be considered as part of a new subfamily. [provided by RefSeq, Jul 2008]","start":43766533,"end":43781257,"strand":-1,"description":"potassium calcium-activated channel subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:6293]"}, {"versioned_ensembl_gene_id":"ENSG00000226592.1","gene_symbol":"AC004911.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145269514,"end":145270384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254911.3","gene_symbol":"SCARNA9","gene_name":"small Cajal body-specific RNA 9 [Source:HGNC Symbol;Acc:HGNC:32566]","synonyms":"Z32,mgU2-19/30","biotype":"antisense_RNA","ncbi_id":"619383","summary":null,"start":93721513,"end":93721865,"strand":1,"description":"small Cajal body-specific RNA 9 [Source:HGNC Symbol;Acc:HGNC:32566]"}, {"versioned_ensembl_gene_id":"ENSG00000280405.1","gene_symbol":"AC026336.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130144954,"end":130145691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230595.1","gene_symbol":"RSL24D1P2","gene_name":"ribosomal L24 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129162","summary":null,"start":62561058,"end":62561423,"strand":-1,"description":"ribosomal L24 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37867]"}, {"versioned_ensembl_gene_id":"ENSG00000276825.2","gene_symbol":"DRD4","gene_name":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1815","summary":"This gene encodes the D4 subtype of the dopamine receptor. The D4 subtype is a G-protein coupled receptor which inhibits adenylyl cyclase. It is a target for drugs which treat schizophrenia and Parkinson disease. Mutations in this gene have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit/hyperactivity disorder, and the personality trait of novelty seeking. This gene contains a polymorphic number (2-10 copies) of tandem 48 nt repeats; the sequence shown contains four repeats. [provided by RefSeq, Jul 2008]","start":637525,"end":640936,"strand":1,"description":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]"}, {"versioned_ensembl_gene_id":"ENSG00000259029.1","gene_symbol":"DUX4L18","gene_name":"double homeobox 4 like 18 [Source:HGNC Symbol;Acc:HGNC:37716]","synonyms":"DUXY2","biotype":"unprocessed_pseudogene","ncbi_id":"100132421","summary":null,"start":11321557,"end":11322823,"strand":1,"description":"double homeobox 4 like 18 [Source:HGNC Symbol;Acc:HGNC:37716]"}, {"versioned_ensembl_gene_id":"ENSG00000213779.4","gene_symbol":"AC107956.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17193489,"end":17194308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228473.1","gene_symbol":"LIN28AP2","gene_name":"LIN28A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287388","summary":null,"start":87379472,"end":87380258,"strand":-1,"description":"LIN28A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38056]"}, {"versioned_ensembl_gene_id":"ENSG00000184906.10","gene_symbol":"AMYH02020865.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40497850,"end":40566779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124449.6","gene_symbol":"IRGC","gene_name":"immunity related GTPase cinema [Source:HGNC Symbol;Acc:HGNC:28835]","synonyms":"IRGC1,Iigp5,CINEMA","biotype":"protein_coding","ncbi_id":"56269","summary":null,"start":43716010,"end":43720021,"strand":1,"description":"immunity related GTPase cinema [Source:HGNC Symbol;Acc:HGNC:28835]"}, {"versioned_ensembl_gene_id":"ENSG00000161996.18","gene_symbol":"WDR90","gene_name":"WD repeat domain 90 [Source:HGNC Symbol;Acc:HGNC:26960]","synonyms":"C16orf15,KIAA1924,FLJ36483,C16orf19,C16orf18,C16orf17,C16orf16","biotype":"protein_coding","ncbi_id":"197335","summary":null,"start":649311,"end":667833,"strand":1,"description":"WD repeat domain 90 [Source:HGNC Symbol;Acc:HGNC:26960]"}, {"versioned_ensembl_gene_id":"ENSG00000168619.15","gene_symbol":"ADAM18","gene_name":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]","synonyms":"tMDCIII,ADAM27","biotype":"protein_coding","ncbi_id":"8749","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature sperm surface protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":39584489,"end":39730064,"strand":1,"description":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]"}, {"versioned_ensembl_gene_id":"ENSG00000139842.14","gene_symbol":"CUL4A","gene_name":"cullin 4A [Source:HGNC Symbol;Acc:HGNC:2554]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8451","summary":"CUL4A is the ubiquitin ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins (Liu et al., 2009 [PubMed 19481525]).[supplied by OMIM, Oct 2009]","start":113208193,"end":113267108,"strand":1,"description":"cullin 4A [Source:HGNC Symbol;Acc:HGNC:2554]"}, {"versioned_ensembl_gene_id":"ENSG00000274502.1","gene_symbol":"ANKRD20A6P","gene_name":"ankyrin repeat domain 20 family member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728157","summary":null,"start":11173618,"end":11173821,"strand":1,"description":"ankyrin repeat domain 20 family member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37714]"}, {"versioned_ensembl_gene_id":"ENSG00000253784.1","gene_symbol":"AC090735.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72874859,"end":72881740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230293.11","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31722164,"end":31744857,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000105323.16","gene_symbol":"HNRNPUL1","gene_name":"heterogeneous nuclear ribonucleoprotein U like 1 [Source:HGNC Symbol;Acc:HGNC:17011]","synonyms":"HNRPUL1,FLJ12944,E1BAP5,E1B-AP5","biotype":"protein_coding","ncbi_id":"11100","summary":"This gene encodes a nuclear RNA-binding protein of the heterogeneous nuclear ribonucleoprotein (hnRNP) family. This protein binds specifically to adenovirus early-1B-55kDa oncoprotein. It may play an important role in nucleocytoplasmic RNA transport, and its function is modulated by early-1B-55kDa in adenovirus-infected cells. [provided by RefSeq, Mar 2016]","start":41262496,"end":41307598,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein U like 1 [Source:HGNC Symbol;Acc:HGNC:17011]"}, {"versioned_ensembl_gene_id":"ENSG00000262898.1","gene_symbol":"AC139099.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83144131,"end":83177607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172912.4","gene_symbol":"COX6B1P3","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2283]","synonyms":"COX6BP3","biotype":"processed_pseudogene","ncbi_id":"1343","summary":null,"start":40569286,"end":40569895,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2283]"}, {"versioned_ensembl_gene_id":"ENSG00000004487.15","gene_symbol":"KDM1A","gene_name":"lysine demethylase 1A [Source:HGNC Symbol;Acc:HGNC:29079]","synonyms":"LSD1,KIAA0601,KDM1,BHC110,AOF2","biotype":"protein_coding","ncbi_id":"23028","summary":"This gene encodes a nuclear protein containing a SWIRM domain, a FAD-binding motif, and an amine oxidase domain. This protein is a component of several histone deacetylase complexes, though it silences genes by functioning as a histone demethylase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":23019448,"end":23083689,"strand":1,"description":"lysine demethylase 1A [Source:HGNC Symbol;Acc:HGNC:29079]"}, {"versioned_ensembl_gene_id":"ENSG00000164142.15","gene_symbol":"FAM160A1","gene_name":"family with sequence similarity 160 member A1 [Source:HGNC Symbol;Acc:HGNC:34237]","synonyms":"FLJ43373","biotype":"protein_coding","ncbi_id":"729830","summary":null,"start":151409216,"end":151663632,"strand":1,"description":"family with sequence similarity 160 member A1 [Source:HGNC Symbol;Acc:HGNC:34237]"}, {"versioned_ensembl_gene_id":"ENSG00000240553.1","gene_symbol":"AL031428.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23020147,"end":23088058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243385.2","gene_symbol":"AC094085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83201229,"end":83202141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228236.2","gene_symbol":"TXNP5","gene_name":"thioredoxin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49485]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"151276","summary":null,"start":149068596,"end":149068910,"strand":-1,"description":"thioredoxin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49485]"}, {"versioned_ensembl_gene_id":"ENSG00000019582.14","gene_symbol":"CD74","gene_name":"CD74 molecule [Source:HGNC Symbol;Acc:HGNC:1697]","synonyms":"DHLAG","biotype":"protein_coding","ncbi_id":"972","summary":"The protein encoded by this gene associates with class II major histocompatibility complex (MHC) and is an important chaperone that regulates antigen presentation for immune response. It also serves as cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF) which, when bound to the encoded protein, initiates survival pathways and cell proliferation. This protein also interacts with amyloid precursor protein (APP) and suppresses the production of amyloid beta (Abeta). Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":150401637,"end":150412929,"strand":-1,"description":"CD74 molecule [Source:HGNC Symbol;Acc:HGNC:1697]"}, {"versioned_ensembl_gene_id":"ENSG00000254816.1","gene_symbol":"AC090857.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21169748,"end":21170137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270570.1","gene_symbol":"AC140113.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11107719,"end":11107887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283044.1","gene_symbol":"AL391597.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207401691,"end":207416236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243160.1","gene_symbol":"AC093270.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79529302,"end":79530093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275855.1","gene_symbol":"AC138747.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28361822,"end":28365684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225993.9","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"Ly6-D,NG25,G6D,MEGT1,C6orf23","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31754813,"end":31757257,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000217576.7","gene_symbol":"AL158066.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52167709,"end":52291557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117013.14","gene_symbol":"KCNQ4","gene_name":"potassium voltage-gated channel subfamily Q member 4 [Source:HGNC Symbol;Acc:HGNC:6298]","synonyms":"Kv7.4,DFNA2","biotype":"protein_coding","ncbi_id":"9132","summary":"The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":40784012,"end":40840452,"strand":1,"description":"potassium voltage-gated channel subfamily Q member 4 [Source:HGNC Symbol;Acc:HGNC:6298]"}, {"versioned_ensembl_gene_id":"ENSG00000226870.2","gene_symbol":"BX276092.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71719142,"end":71721278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228490.1","gene_symbol":"CT009496.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29881442,"end":29882408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179604.9","gene_symbol":"CDC42EP4","gene_name":"CDC42 effector protein 4 [Source:HGNC Symbol;Acc:HGNC:17147]","synonyms":"BORG4,MGC3740,MGC17125,KAIA1777,CEP4","biotype":"protein_coding","ncbi_id":"23580","summary":"The product of this gene is a member of the CDC42-binding protein family. Members of this family interact with Rho family GTPases and regulate the organization of the actin cytoskeleton. This protein has been shown to bind both CDC42 and TC10 GTPases in a GTP-dependent manner. When overexpressed in fibroblasts, this protein was able to induce pseudopodia formation, which suggested a role in inducing actin filament assembly and cell shape control. [provided by RefSeq, Jul 2008]","start":73283624,"end":73312175,"strand":-1,"description":"CDC42 effector protein 4 [Source:HGNC Symbol;Acc:HGNC:17147]"}, {"versioned_ensembl_gene_id":"ENSG00000253499.2","gene_symbol":"AC025881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114318400,"end":114318911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144468.16","gene_symbol":"RHBDD1","gene_name":"rhomboid domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23081]","synonyms":"DKFZp547E052","biotype":"protein_coding","ncbi_id":"84236","summary":null,"start":226835581,"end":226999215,"strand":1,"description":"rhomboid domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23081]"}, {"versioned_ensembl_gene_id":"ENSG00000253226.1","gene_symbol":"HAUS1P3","gene_name":"HAUS augmin like complex subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271703","summary":null,"start":72618722,"end":72619383,"strand":-1,"description":"HAUS augmin like complex subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43762]"}, {"versioned_ensembl_gene_id":"ENSG00000153187.18","gene_symbol":"HNRNPU","gene_name":"heterogeneous nuclear ribonucleoprotein U [Source:HGNC Symbol;Acc:HGNC:5048]","synonyms":"HNRNPU-AS1,hnRNPU,FLJ37978,FLJ30202,C1orf199,SAF-A,NCRNA00201,HNRPU","biotype":"protein_coding","ncbi_id":"3192","summary":"This gene encodes a member of a family of proteins that bind nucleic acids and function in the formation of ribonucleoprotein complexes in the nucleus with heterogeneous nuclear RNA (hnRNA). The encoded protein has affinity for both RNA and DNA, and binds scaffold-attached region (SAR) DNA. Mutations in this gene have been associated with epileptic encephalopathy, early infantile, 54. A pseudogene of this gene has been identified on chromosome 14. [provided by RefSeq, Jun 2017]","start":244840638,"end":244864560,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein U [Source:HGNC Symbol;Acc:HGNC:5048]"}, {"versioned_ensembl_gene_id":"ENSG00000198520.10","gene_symbol":"C1orf228","gene_name":"chromosome 1 open reading frame 228 [Source:HGNC Symbol;Acc:HGNC:34345]","synonyms":"p40,NCRNA00082,MGC33556","biotype":"protein_coding","ncbi_id":"339541","summary":null,"start":44674692,"end":44725591,"strand":1,"description":"chromosome 1 open reading frame 228 [Source:HGNC Symbol;Acc:HGNC:34345]"}, {"versioned_ensembl_gene_id":"ENSG00000176893.5","gene_symbol":"OR51G2","gene_name":"olfactory receptor family 51 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81282","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4912588,"end":4919350,"strand":-1,"description":"olfactory receptor family 51 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15198]"}, {"versioned_ensembl_gene_id":"ENSG00000235441.5","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"OR10C1P,hs6M1-17,OR10C2","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439782,"end":29441453,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000279261.2","gene_symbol":"AL360294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234757619,"end":234760056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149970.14","gene_symbol":"CNKSR2","gene_name":"connector enhancer of kinase suppressor of Ras 2 [Source:HGNC Symbol;Acc:HGNC:19701]","synonyms":"KSR2,KIAA0902,CNK2","biotype":"protein_coding","ncbi_id":"22866","summary":"This gene encodes a multidomain protein that functions as a scaffold protein to mediate the mitogen-activated protein kinase pathways downstream from Ras. This gene product is induced by vitamin D and inhibits apoptosis in certain cancer cells. It may also play a role in ternary complex assembly of synaptic proteins at the postsynaptic membrane and coupling of signal transduction to membrane/cytoskeletal remodeling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":21374418,"end":21654695,"strand":1,"description":"connector enhancer of kinase suppressor of Ras 2 [Source:HGNC Symbol;Acc:HGNC:19701]"}, {"versioned_ensembl_gene_id":"ENSG00000229309.2","gene_symbol":"AL353633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81250438,"end":81302407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248778.1","gene_symbol":"AC105391.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105679050,"end":105680094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144031.11","gene_symbol":"ANKRD53","gene_name":"ankyrin repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:25691]","synonyms":"FLJ12056,FLJ36160","biotype":"protein_coding","ncbi_id":"79998","summary":null,"start":70978380,"end":70985499,"strand":1,"description":"ankyrin repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:25691]"}, {"versioned_ensembl_gene_id":"ENSG00000239322.1","gene_symbol":"ATP6V1B1-AS1","gene_name":"ATP6V1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51118]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927750","summary":null,"start":70941817,"end":70948610,"strand":-1,"description":"ATP6V1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51118]"}, {"versioned_ensembl_gene_id":"ENSG00000236699.8","gene_symbol":"ARHGEF38","gene_name":"Rho guanine nucleotide exchange factor 38 [Source:HGNC Symbol;Acc:HGNC:25968]","synonyms":"FLJ20184","biotype":"protein_coding","ncbi_id":"54848","summary":null,"start":105552620,"end":105708093,"strand":1,"description":"Rho guanine nucleotide exchange factor 38 [Source:HGNC Symbol;Acc:HGNC:25968]"}, {"versioned_ensembl_gene_id":"ENSG00000226061.1","gene_symbol":"PCMTD1P1","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38804]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874520","summary":null,"start":10173853,"end":10174207,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38804]"}, {"versioned_ensembl_gene_id":"ENSG00000250120.6","gene_symbol":"PCDHA10","gene_name":"protocadherin alpha 10 [Source:HGNC Symbol;Acc:HGNC:8664]","synonyms":"PCDH-ALPHA10,CRNR8,CNRS8,CNRN8,CNR8","biotype":"protein_coding","ncbi_id":"56139","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140855883,"end":141012344,"strand":1,"description":"protocadherin alpha 10 [Source:HGNC Symbol;Acc:HGNC:8664]"}, {"versioned_ensembl_gene_id":"ENSG00000224058.2","gene_symbol":"AC006509.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47731402,"end":47732035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235369.1","gene_symbol":"RPL36AP15","gene_name":"ribosomal protein L36a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271325","summary":null,"start":47797826,"end":47798091,"strand":-1,"description":"ribosomal protein L36a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36648]"}, {"versioned_ensembl_gene_id":"ENSG00000254961.1","gene_symbol":"TUBB4BP4","gene_name":"tubulin beta 4B class IVb pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480434","summary":null,"start":91949731,"end":91950034,"strand":-1,"description":"tubulin beta 4B class IVb pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42333]"}, {"versioned_ensembl_gene_id":"ENSG00000169047.5","gene_symbol":"IRS1","gene_name":"insulin receptor substrate 1 [Source:HGNC Symbol;Acc:HGNC:6125]","synonyms":"HIRS-1","biotype":"protein_coding","ncbi_id":"3667","summary":"This gene encodes a protein which is phosphorylated by insulin receptor tyrosine kinase. Mutations in this gene are associated with type II diabetes and susceptibility to insulin resistance. [provided by RefSeq, Nov 2009]","start":226731317,"end":226799759,"strand":-1,"description":"insulin receptor substrate 1 [Source:HGNC Symbol;Acc:HGNC:6125]"}, {"versioned_ensembl_gene_id":"ENSG00000235070.3","gene_symbol":"AC062015.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":226180044,"end":226185371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279417.1","gene_symbol":"AC019322.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30344307,"end":30348236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251664.3","gene_symbol":"PCDHA12","gene_name":"protocadherin alpha 12 [Source:HGNC Symbol;Acc:HGNC:8666]","synonyms":"PCDH-ALPHA12","biotype":"protein_coding","ncbi_id":"56137","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140875302,"end":141012344,"strand":1,"description":"protocadherin alpha 12 [Source:HGNC Symbol;Acc:HGNC:8666]"}, {"versioned_ensembl_gene_id":"ENSG00000254026.1","gene_symbol":"AC015468.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20954012,"end":20968904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253199.1","gene_symbol":"LINC02153","gene_name":"long intergenic non-protein coding RNA 2153 [Source:HGNC Symbol;Acc:HGNC:27823]","synonyms":"ENST00000517573","biotype":"lincRNA","ncbi_id":"286114","summary":null,"start":20973797,"end":20995119,"strand":1,"description":"long intergenic non-protein coding RNA 2153 [Source:HGNC Symbol;Acc:HGNC:27823]"}, {"versioned_ensembl_gene_id":"ENSG00000086015.20","gene_symbol":"MAST2","gene_name":"microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:19035]","synonyms":"MAST205,KIAA0807","biotype":"protein_coding","ncbi_id":"23139","summary":null,"start":45786987,"end":46036124,"strand":1,"description":"microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:19035]"}, {"versioned_ensembl_gene_id":"ENSG00000116062.14","gene_symbol":"MSH6","gene_name":"mutS homolog 6 [Source:HGNC Symbol;Acc:HGNC:7329]","synonyms":"GTBP","biotype":"protein_coding","ncbi_id":"2956","summary":"This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a bidirectional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]","start":47695530,"end":47810101,"strand":1,"description":"mutS homolog 6 [Source:HGNC Symbol;Acc:HGNC:7329]"}, {"versioned_ensembl_gene_id":"ENSG00000279744.1","gene_symbol":"AC132938.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82462601,"end":82464255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248468.1","gene_symbol":"AC107027.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131517831,"end":131520880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172410.4","gene_symbol":"INSL5","gene_name":"insulin like 5 [Source:HGNC Symbol;Acc:HGNC:6088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10022","summary":"The protein encoded by this gene contains a classical signature of the insulin superfamily and is highly similar to relaxin 3 (RLN3/INSL7). [provided by RefSeq, Jul 2008]","start":66797741,"end":66801256,"strand":-1,"description":"insulin like 5 [Source:HGNC Symbol;Acc:HGNC:6088]"}, {"versioned_ensembl_gene_id":"ENSG00000167910.3","gene_symbol":"CYP7A1","gene_name":"cytochrome P450 family 7 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2651]","synonyms":"CYP7","biotype":"protein_coding","ncbi_id":"1581","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway in the liver, which converts cholesterol to bile acids. This reaction is the rate limiting step and the major site of regulation of bile acid synthesis, which is the primary mechanism for the removal of cholesterol from the body. Polymorphisms in the promoter of this gene are associated with defects in bile acid synthesis. [provided by RefSeq, Feb 2010]","start":58490178,"end":58500236,"strand":-1,"description":"cytochrome P450 family 7 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2651]"}, {"versioned_ensembl_gene_id":"ENSG00000250195.1","gene_symbol":"AC109927.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138819954,"end":139012646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070214.15","gene_symbol":"SLC44A1","gene_name":"solute carrier family 44 member 1 [Source:HGNC Symbol;Acc:HGNC:18798]","synonyms":"CTL1,CHTL1,CDW92,CD92","biotype":"protein_coding","ncbi_id":"23446","summary":null,"start":105244622,"end":105439171,"strand":1,"description":"solute carrier family 44 member 1 [Source:HGNC Symbol;Acc:HGNC:18798]"}, {"versioned_ensembl_gene_id":"ENSG00000224712.12","gene_symbol":"NPIPA3","gene_name":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642778","summary":null,"start":14708944,"end":14726338,"strand":1,"description":"nuclear pore complex interacting protein family member A3 [Source:HGNC Symbol;Acc:HGNC:41978]"}, {"versioned_ensembl_gene_id":"ENSG00000185238.12","gene_symbol":"PRMT3","gene_name":"protein arginine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30163]","synonyms":"HRMT1L3","biotype":"protein_coding","ncbi_id":"10196","summary":"This gene belongs to the protein arginine methyltransferase (PRMT) family. The encoded enzyme catalyzes the methylation of guanidino nitrogens of arginyl residues of proteins. The enzyme acts on 40S ribosomal protein S2 (rpS2), which is its major in-vivo substrate, and is involved in the proper maturation of the 80S ribosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":20387530,"end":20509294,"strand":1,"description":"protein arginine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30163]"}, {"versioned_ensembl_gene_id":"ENSG00000213673.3","gene_symbol":"SLC25A5P3","gene_name":"solute carrier family 25 member 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:507]","synonyms":"ANTP1","biotype":"processed_pseudogene","ncbi_id":"222005","summary":null,"start":54419444,"end":54420328,"strand":1,"description":"solute carrier family 25 member 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:507]"}, {"versioned_ensembl_gene_id":"ENSG00000124767.6","gene_symbol":"GLO1","gene_name":"glyoxalase I [Source:HGNC Symbol;Acc:HGNC:4323]","synonyms":"GLOD1","biotype":"protein_coding","ncbi_id":"2739","summary":"The enzyme encoded by this gene is responsible for the catalysis and formation of S-lactoyl-glutathione from methylglyoxal condensation and reduced glutatione. Glyoxalase I is linked to HLA and is localized to 6p21.3-p21.1, between HLA and the centromere. [provided by RefSeq, Jul 2008]","start":38675925,"end":38703141,"strand":-1,"description":"glyoxalase I [Source:HGNC Symbol;Acc:HGNC:4323]"}, {"versioned_ensembl_gene_id":"ENSG00000171431.3","gene_symbol":"KRT20","gene_name":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]","synonyms":"K20,CK20,MGC35423","biotype":"protein_coding","ncbi_id":"54474","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This cytokeratin is a major cellular protein of mature enterocytes and goblet cells and is specifically expressed in the gastric and intestinal mucosa. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2008]","start":40875941,"end":40885227,"strand":-1,"description":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]"}, {"versioned_ensembl_gene_id":"ENSG00000261399.1","gene_symbol":"AL031710.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1713527,"end":1714208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230054.2","gene_symbol":"AL160275.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":114656304,"end":114662374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254888.2","gene_symbol":"AP000827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90074839,"end":90075096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231874.3","gene_symbol":"TSPY18P","gene_name":"testis specific protein, Y-linked 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:37725]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642796","summary":null,"start":9869664,"end":9870781,"strand":1,"description":"testis specific protein, Y-linked 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:37725]"}, {"versioned_ensembl_gene_id":"ENSG00000182459.4","gene_symbol":"TEX19","gene_name":"testis expressed 19 [Source:HGNC Symbol;Acc:HGNC:33802]","synonyms":"FLJ35767","biotype":"protein_coding","ncbi_id":"400629","summary":null,"start":82359247,"end":82363776,"strand":1,"description":"testis expressed 19 [Source:HGNC Symbol;Acc:HGNC:33802]"}, {"versioned_ensembl_gene_id":"ENSG00000109113.19","gene_symbol":"RAB34","gene_name":"RAB34, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16519]","synonyms":"RAH,RAB39,NARR","biotype":"protein_coding","ncbi_id":"83871","summary":"This gene encodes a protein belonging to the RAB family of proteins, which are small GTPases involved in protein transport. This family member is a Golgi-bound member of the secretory pathway that is involved in the repositioning of lysosomes and the activation of macropinocytosis. Alternative splicing of this gene results in multiple transcript variants. An alternatively spliced transcript variant produces the nine-amino acid residue-repeats (NARR) protein, which is a functionally distinct nucleolar protein resulting from a different reading frame. [provided by RefSeq, Dec 2016]","start":28714281,"end":28718429,"strand":-1,"description":"RAB34, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16519]"}, {"versioned_ensembl_gene_id":"ENSG00000230896.1","gene_symbol":"AL604028.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45694684,"end":45697075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255187.1","gene_symbol":"AP003386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91158083,"end":91167294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127328.21","gene_symbol":"RAB3IP","gene_name":"RAB3A interacting protein [Source:HGNC Symbol;Acc:HGNC:16508]","synonyms":"RABIN8,RABIN3,FLJ22548","biotype":"protein_coding","ncbi_id":"117177","summary":null,"start":69738681,"end":69823204,"strand":1,"description":"RAB3A interacting protein [Source:HGNC Symbol;Acc:HGNC:16508]"}, {"versioned_ensembl_gene_id":"ENSG00000174165.7","gene_symbol":"ZDHHC24","gene_name":"zinc finger DHHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:27387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"254359","summary":null,"start":66520637,"end":66546238,"strand":-1,"description":"zinc finger DHHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:27387]"}, {"versioned_ensembl_gene_id":"ENSG00000089723.9","gene_symbol":"OTUB2","gene_name":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]","synonyms":"MGC3102,FLJ21916,C14orf137","biotype":"protein_coding","ncbi_id":"78990","summary":"This gene encodes one of several deubiquitylating enzymes. Ubiquitin modification of proteins is needed for their stability and function; to reverse the process, deubiquityling enzymes remove ubiquitin. This protein contains an OTU domain and binds Ubal (ubiquitin aldehyde); an active cysteine protease site is present in the OTU domain. [provided by RefSeq, Aug 2011]","start":94026329,"end":94048930,"strand":1,"description":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]"}, {"versioned_ensembl_gene_id":"ENSG00000093000.18","gene_symbol":"NUP50","gene_name":"nucleoporin 50 [Source:HGNC Symbol;Acc:HGNC:8065]","synonyms":"NPAP60L","biotype":"protein_coding","ncbi_id":"10762","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of the FG-repeat containing nucleoporins that functions as a soluble cofactor in importin-alpha:beta-mediated nuclear protein import. Pseudogenes of this gene are found on chromosomes 5, 6, and 14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":45163841,"end":45188015,"strand":1,"description":"nucleoporin 50 [Source:HGNC Symbol;Acc:HGNC:8065]"}, {"versioned_ensembl_gene_id":"ENSG00000139133.6","gene_symbol":"ALG10","gene_name":"ALG10, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23162]","synonyms":"FLJ14751,DIE2,ALG10A","biotype":"protein_coding","ncbi_id":"84920","summary":"This gene encodes a membrane-associated protein that adds the third glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation. That is, it transfers the terminal glucose from dolichyl phosphate glucose (Dol-P-Glc) onto the lipid-linked oligosaccharide Glc2Man9GlcNAc(2)-PP-Dol. The rat protein homolog was shown to specifically modulate the gating function of the rat neuronal ether-a-go-go (EAG) potassium ion channel. [provided by RefSeq, Jan 2010]","start":34022281,"end":34029694,"strand":1,"description":"ALG10, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23162]"}, {"versioned_ensembl_gene_id":"ENSG00000269235.1","gene_symbol":"ZNF350-AS1","gene_name":"ZNF350 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48598]","synonyms":"uc002pyc,HCCAT3","biotype":"antisense_RNA","ncbi_id":"101669766","summary":null,"start":51949134,"end":51981367,"strand":1,"description":"ZNF350 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48598]"}, {"versioned_ensembl_gene_id":"ENSG00000270987.1","gene_symbol":"AL133338.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100889603,"end":100890338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282221.1","gene_symbol":"AC119427.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201399633,"end":201401190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266654.1","gene_symbol":"AC129510.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82160056,"end":82160452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258458.5","gene_symbol":"AL160314.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22702611,"end":22766562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213050.5","gene_symbol":"TPM3P1","gene_name":"tropomyosin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16350]","synonyms":"TPM3L2","biotype":"processed_pseudogene","ncbi_id":"252956","summary":null,"start":116972165,"end":116972911,"strand":-1,"description":"tropomyosin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16350]"}, {"versioned_ensembl_gene_id":"ENSG00000277024.1","gene_symbol":"BX005214.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":39359890,"end":39369105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259706.1","gene_symbol":"HSP90B2P","gene_name":"heat shock protein 90 beta family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12099]","synonyms":"TRAP1,TRA1P1,HSPCP2,GRP94P1,GRP94b","biotype":"processed_pseudogene","ncbi_id":"7190","summary":null,"start":99257632,"end":99260015,"strand":1,"description":"heat shock protein 90 beta family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12099]"}, {"versioned_ensembl_gene_id":"ENSG00000259257.1","gene_symbol":"AC037479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99337857,"end":99338481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215112.6","gene_symbol":"FAM74A1","gene_name":"family with sequence similarity 74 member A1 [Source:HGNC Symbol;Acc:HGNC:32029]","synonyms":"FAM74A5","biotype":"lincRNA","ncbi_id":"401507","summary":null,"start":39371065,"end":39376916,"strand":1,"description":"family with sequence similarity 74 member A1 [Source:HGNC Symbol;Acc:HGNC:32029]"}, {"versioned_ensembl_gene_id":"ENSG00000155463.12","gene_symbol":"OXA1L","gene_name":"OXA1L, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:8526]","synonyms":"OXA1,MGC133129","biotype":"protein_coding","ncbi_id":"5018","summary":"This gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N-terminal tail of subunit 2 of cytochrome c oxidase, and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2016]","start":22766522,"end":22773041,"strand":1,"description":"OXA1L, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:8526]"}, {"versioned_ensembl_gene_id":"ENSG00000259392.2","gene_symbol":"AC090877.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32836983,"end":32837326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259228.1","gene_symbol":"HNRNPA1P62","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48792]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480235","summary":null,"start":99284625,"end":99285576,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:48792]"}, {"versioned_ensembl_gene_id":"ENSG00000279958.1","gene_symbol":"AC019278.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33105758,"end":33106236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146414.15","gene_symbol":"SHPRH","gene_name":"SNF2 histone linker PHD RING helicase [Source:HGNC Symbol;Acc:HGNC:19336]","synonyms":"KIAA2023,FLJ90837,bA545I5.2","biotype":"protein_coding","ncbi_id":"257218","summary":"SHPRH is a ubiquitously expressed protein that contains motifs characteristics of several DNA repair proteins, transcription factors, and helicases. SHPRH is a functional homolog of S. cerevisiae RAD5 (Unk et al., 2006 [PubMed 17108083]).[supplied by OMIM, Mar 2008]","start":145864245,"end":145964423,"strand":-1,"description":"SNF2 histone linker PHD RING helicase [Source:HGNC Symbol;Acc:HGNC:19336]"}, {"versioned_ensembl_gene_id":"ENSG00000004866.20","gene_symbol":"ST7","gene_name":"suppression of tumorigenicity 7 [Source:HGNC Symbol;Acc:HGNC:11351]","synonyms":"TSG7,SEN4,RAY1,HELG,FAM4A1,FAM4A,ETS7q","biotype":"protein_coding","ncbi_id":"7982","summary":"The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]","start":116953238,"end":117230103,"strand":1,"description":"suppression of tumorigenicity 7 [Source:HGNC Symbol;Acc:HGNC:11351]"}, {"versioned_ensembl_gene_id":"ENSG00000252336.1","gene_symbol":"RNA5SP148","gene_name":"RNA, 5S ribosomal pseudogene 148 [Source:HGNC Symbol;Acc:HGNC:43048]","synonyms":"RN5S148","biotype":"rRNA","ncbi_id":"100873415","summary":null,"start":178429197,"end":178429290,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 148 [Source:HGNC Symbol;Acc:HGNC:43048]"}, {"versioned_ensembl_gene_id":"ENSG00000259686.1","gene_symbol":"HNRNPA1P71","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:48801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421433","summary":null,"start":33012119,"end":33013068,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:48801]"}, {"versioned_ensembl_gene_id":"ENSG00000168904.14","gene_symbol":"LRRC28","gene_name":"leucine rich repeat containing 28 [Source:HGNC Symbol;Acc:HGNC:28355]","synonyms":"MGC24976,FLJ45242,FLJ34269","biotype":"protein_coding","ncbi_id":"123355","summary":null,"start":99251362,"end":99390729,"strand":1,"description":"leucine rich repeat containing 28 [Source:HGNC Symbol;Acc:HGNC:28355]"}, {"versioned_ensembl_gene_id":"ENSG00000250330.1","gene_symbol":"AC016559.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79229904,"end":79230588,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229208.1","gene_symbol":"RBMY2NP","gene_name":"RNA binding motif protein, Y-linked, family 2, member N pseudogene [Source:HGNC Symbol;Acc:HGNC:23919]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378956","summary":null,"start":9831418,"end":9846696,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member N pseudogene [Source:HGNC Symbol;Acc:HGNC:23919]"}, {"versioned_ensembl_gene_id":"ENSG00000233123.1","gene_symbol":"LINC01007","gene_name":"long intergenic non-protein coding RNA 1007 [Source:HGNC Symbol;Acc:HGNC:48973]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506527","summary":null,"start":101562779,"end":101569006,"strand":-1,"description":"long intergenic non-protein coding RNA 1007 [Source:HGNC Symbol;Acc:HGNC:48973]"}, {"versioned_ensembl_gene_id":"ENSG00000273853.1","gene_symbol":"AC023158.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33432311,"end":33432853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259937.2","gene_symbol":"AC023158.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33404872,"end":33405896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123843.12","gene_symbol":"C4BPB","gene_name":"complement component 4 binding protein beta [Source:HGNC Symbol;Acc:HGNC:1328]","synonyms":"C4BP","biotype":"protein_coding","ncbi_id":"725","summary":"This gene encodes a member of a superfamily of proteins composed predominantly of tandemly arrayed short consensus repeats of approximately 60 amino acids. A single, unique beta-chain encoded by this gene assembles with seven identical alpha-chains into the predominant isoform of C4b-binding protein, a multimeric protein that controls activation of the complement cascade through the classical pathway. C4b-binding protein has a regulatory role in the coagulation system also, mediated through the beta-chain binding of protein S, a vitamin K-dependent protein that serves as a cofactor of activated protein C. The genes encoding both alpha and beta chains are located adjacent to each other on human chromosome 1 in the regulator of complement activation gene cluster. Alternative splicing gives rise to multiple transcript variants. [provided by RefSeq, Jul 2008]","start":207088842,"end":207099993,"strand":1,"description":"complement component 4 binding protein beta [Source:HGNC Symbol;Acc:HGNC:1328]"}, {"versioned_ensembl_gene_id":"ENSG00000282459.1","gene_symbol":"TRBV6-6","gene_name":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]","synonyms":"TRBV66,TCRBV6S6,TCRBV13S6A2T","biotype":"TR_V_gene","ncbi_id":"28601","summary":null,"start":142491254,"end":142491732,"strand":1,"description":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]"}, {"versioned_ensembl_gene_id":"ENSG00000216098.1","gene_symbol":"MIR892B","gene_name":"microRNA 892b [Source:HGNC Symbol;Acc:HGNC:33649]","synonyms":"MIRN892B,hsa-mir-892b","biotype":"miRNA","ncbi_id":"100126307","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145997198,"end":145997274,"strand":-1,"description":"microRNA 892b [Source:HGNC Symbol;Acc:HGNC:33649]"}, {"versioned_ensembl_gene_id":"ENSG00000212601.1","gene_symbol":"RNA5SP53","gene_name":"RNA, 5S ribosomal pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:42830]","synonyms":"RN5S53","biotype":"rRNA","ncbi_id":"100873291","summary":null,"start":93488333,"end":93488452,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:42830]"}, {"versioned_ensembl_gene_id":"ENSG00000199857.1","gene_symbol":"SNORD50","gene_name":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":76402076,"end":76402146,"strand":1,"description":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]"}, {"versioned_ensembl_gene_id":"ENSG00000201638.2","gene_symbol":"RNY4P16","gene_name":"RNA, Ro-associated Y4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:34066]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100431173","summary":null,"start":234837976,"end":234838069,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:34066]"}, {"versioned_ensembl_gene_id":"ENSG00000276746.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33562880,"end":33563130,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284142.1","gene_symbol":"MIR6845","gene_name":"microRNA 6845 [Source:HGNC Symbol;Acc:HGNC:49956]","synonyms":"hsa-mir-6845","biotype":"miRNA","ncbi_id":"102466748","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143837756,"end":143837816,"strand":-1,"description":"microRNA 6845 [Source:HGNC Symbol;Acc:HGNC:49956]"}, {"versioned_ensembl_gene_id":"ENSG00000243359.3","gene_symbol":"RN7SL815P","gene_name":"RNA, 7SL, cytoplasmic 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:46831]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479519","summary":null,"start":115837870,"end":115838159,"strand":1,"description":"RNA, 7SL, cytoplasmic 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:46831]"}, {"versioned_ensembl_gene_id":"ENSG00000207746.1","gene_symbol":"MIR575","gene_name":"microRNA 575 [Source:HGNC Symbol;Acc:HGNC:32831]","synonyms":"MIRN575,hsa-mir-575","biotype":"miRNA","ncbi_id":"693160","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82753337,"end":82753430,"strand":-1,"description":"microRNA 575 [Source:HGNC Symbol;Acc:HGNC:32831]"}, {"versioned_ensembl_gene_id":"ENSG00000280263.1","gene_symbol":"ACTR3BP2","gene_name":"ACTR3B pseudogene 2 [Source:NCBI gene;Acc:440888]","synonyms":"FKSG73,FKSG73","biotype":"processed_pseudogene","ncbi_id":"440888","summary":null,"start":16486985,"end":16488322,"strand":1,"description":"ACTR3B pseudogene 2 [Source:NCBI gene;Acc:440888]"}, {"versioned_ensembl_gene_id":"ENSG00000207267.1","gene_symbol":"RNU6-1081P","gene_name":"RNA, U6 small nuclear 1081, pseudogene [Source:HGNC Symbol;Acc:HGNC:48044]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480636","summary":null,"start":11233988,"end":11234094,"strand":1,"description":"RNA, U6 small nuclear 1081, pseudogene [Source:HGNC Symbol;Acc:HGNC:48044]"}, {"versioned_ensembl_gene_id":"ENSG00000267583.5","gene_symbol":"AC007998.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35443869,"end":35467088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266383.1","gene_symbol":"MIR5002","gene_name":"microRNA 5002 [Source:HGNC Symbol;Acc:HGNC:43470]","synonyms":"hsa-mir-5002","biotype":"miRNA","ncbi_id":"100847021","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124132929,"end":124133025,"strand":1,"description":"microRNA 5002 [Source:HGNC Symbol;Acc:HGNC:43470]"}, {"versioned_ensembl_gene_id":"ENSG00000266015.1","gene_symbol":"MIR4309","gene_name":"microRNA 4309 [Source:HGNC Symbol;Acc:HGNC:38336]","synonyms":"hsa-mir-4309","biotype":"miRNA","ncbi_id":"100422954","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102539644,"end":102539726,"strand":1,"description":"microRNA 4309 [Source:HGNC Symbol;Acc:HGNC:38336]"}, {"versioned_ensembl_gene_id":"ENSG00000264902.1","gene_symbol":"MIR5701-3","gene_name":"microRNA 5701-3 [Source:HGNC Symbol;Acc:HGNC:50844]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504741","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21951242,"end":21951323,"strand":1,"description":"microRNA 5701-3 [Source:HGNC Symbol;Acc:HGNC:50844]"}, {"versioned_ensembl_gene_id":"ENSG00000243005.3","gene_symbol":"RN7SL16P","gene_name":"RNA, 7SL, cytoplasmic 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46032]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479231","summary":null,"start":24563193,"end":24563461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46032]"}, {"versioned_ensembl_gene_id":"ENSG00000273658.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53464720,"end":53464901,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000264881.1","gene_symbol":"MIR1273D","gene_name":"microRNA 1273d [Source:HGNC Symbol;Acc:HGNC:38375]","synonyms":"hsa-mir-1273d","biotype":"miRNA","ncbi_id":"100422970","summary":"This record was withdrawn by miRBase.","start":10227718,"end":10227803,"strand":1,"description":"microRNA 1273d [Source:HGNC Symbol;Acc:HGNC:38375]"}, {"versioned_ensembl_gene_id":"ENSG00000275054.1","gene_symbol":"ST7-OT3_1","gene_name":"ST7 overlapping transcript 3 conserved region 1 [Source:RFAM;Acc:RF02183]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117184126,"end":117184199,"strand":1,"description":"ST7 overlapping transcript 3 conserved region 1 [Source:RFAM;Acc:RF02183]"}, {"versioned_ensembl_gene_id":"ENSG00000252720.1","gene_symbol":"RNU6-1258P","gene_name":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480115","summary":null,"start":93437400,"end":93437510,"strand":-1,"description":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]"}, {"versioned_ensembl_gene_id":"ENSG00000278454.1","gene_symbol":"ZFAT-AS1_3","gene_name":"ZFAT antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02213]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":134600257,"end":134600336,"strand":1,"description":"ZFAT antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02213]"}, {"versioned_ensembl_gene_id":"ENSG00000274520.1","gene_symbol":"Six3os1_1","gene_name":"Six3os1 conserved region 1 [Source:RFAM;Acc:RF02246]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44932320,"end":44932406,"strand":1,"description":"Six3os1 conserved region 1 [Source:RFAM;Acc:RF02246]"}, {"versioned_ensembl_gene_id":"ENSG00000222743.1","gene_symbol":"RNU6-1190P","gene_name":"RNA, U6 small nuclear 1190, pseudogene [Source:HGNC Symbol;Acc:HGNC:48153]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480087","summary":null,"start":37619985,"end":37620088,"strand":-1,"description":"RNA, U6 small nuclear 1190, pseudogene [Source:HGNC Symbol;Acc:HGNC:48153]"}, {"versioned_ensembl_gene_id":"ENSG00000222574.1","gene_symbol":"RN7SKP61","gene_name":"RNA, 7SK small nuclear pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:45785]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479122","summary":null,"start":78161698,"end":78161992,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:45785]"}, {"versioned_ensembl_gene_id":"ENSG00000200351.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":98936638,"end":98936747,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251779.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76319376,"end":76319473,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252358.1","gene_symbol":"RN7SKP135","gene_name":"RNA, 7SK small nuclear pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:45859]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480875","summary":null,"start":63609354,"end":63609600,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:45859]"}, {"versioned_ensembl_gene_id":"ENSG00000252098.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27255464,"end":27255567,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243642.3","gene_symbol":"RN7SL526P","gene_name":"RNA, 7SL, cytoplasmic 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:46542]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479415","summary":null,"start":58069970,"end":58070288,"strand":1,"description":"RNA, 7SL, cytoplasmic 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:46542]"}, {"versioned_ensembl_gene_id":"ENSG00000222667.1","gene_symbol":"RNU6-394P","gene_name":"RNA, U6 small nuclear 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:47357]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480698","summary":null,"start":66676258,"end":66676364,"strand":-1,"description":"RNA, U6 small nuclear 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:47357]"}, {"versioned_ensembl_gene_id":"ENSG00000238783.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30355436,"end":30355540,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241866.3","gene_symbol":"RN7SL401P","gene_name":"RNA, 7SL, cytoplasmic 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:46417]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480507","summary":null,"start":73744935,"end":73745232,"strand":1,"description":"RNA, 7SL, cytoplasmic 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:46417]"}, {"versioned_ensembl_gene_id":"ENSG00000199477.1","gene_symbol":"SNORA31","gene_name":"small nucleolar RNA, H/ACA box 31 [Source:HGNC Symbol;Acc:HGNC:32621]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":45337480,"end":45337609,"strand":-1,"description":"small nucleolar RNA, H/ACA box 31 [Source:HGNC Symbol;Acc:HGNC:32621]"}, {"versioned_ensembl_gene_id":"ENSG00000200231.1","gene_symbol":"RNU1-23P","gene_name":"RNA, U1 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:41964]","synonyms":null,"biotype":"snRNA","ncbi_id":"106478980","summary":null,"start":24237255,"end":24237398,"strand":1,"description":"RNA, U1 small nuclear 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:41964]"}, {"versioned_ensembl_gene_id":"ENSG00000278732.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31975167,"end":31975448,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000198551.9","gene_symbol":"ZNF627","gene_name":"zinc finger protein 627 [Source:HGNC Symbol;Acc:HGNC:30570]","synonyms":"FLJ90365","biotype":"protein_coding","ncbi_id":"199692","summary":null,"start":11559374,"end":11619135,"strand":1,"description":"zinc finger protein 627 [Source:HGNC Symbol;Acc:HGNC:30570]"}, {"versioned_ensembl_gene_id":"ENSG00000238517.1","gene_symbol":"MIR1270","gene_name":"microRNA 1270 [Source:HGNC Symbol;Acc:HGNC:35338]","synonyms":"MIRN1270,MIR1270-2,MIR1270-1,hsa-mir-1270-2,hsa-mir-1270","biotype":"miRNA","ncbi_id":"100302179","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20399272,"end":20399354,"strand":-1,"description":"microRNA 1270 [Source:HGNC Symbol;Acc:HGNC:35338]"}, {"versioned_ensembl_gene_id":"ENSG00000207559.1","gene_symbol":"MIR578","gene_name":"microRNA 578 [Source:HGNC Symbol;Acc:HGNC:32834]","synonyms":"MIRN578,hsa-mir-578","biotype":"miRNA","ncbi_id":"693163","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":165386242,"end":165386337,"strand":1,"description":"microRNA 578 [Source:HGNC Symbol;Acc:HGNC:32834]"}, {"versioned_ensembl_gene_id":"ENSG00000201529.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67617302,"end":67617415,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284158.1","gene_symbol":"MIR6822","gene_name":"microRNA 6822 [Source:HGNC Symbol;Acc:HGNC:49999]","synonyms":"hsa-mir-6822","biotype":"miRNA","ncbi_id":"102466743","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39138206,"end":39138266,"strand":1,"description":"microRNA 6822 [Source:HGNC Symbol;Acc:HGNC:49999]"}, {"versioned_ensembl_gene_id":"ENSG00000278418.1","gene_symbol":"MIR6512","gene_name":"microRNA 6512 [Source:HGNC Symbol;Acc:HGNC:50259]","synonyms":"hsa-mir-6512","biotype":"miRNA","ncbi_id":"102465255","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177313806,"end":177313882,"strand":-1,"description":"microRNA 6512 [Source:HGNC Symbol;Acc:HGNC:50259]"}, {"versioned_ensembl_gene_id":"ENSG00000201452.1","gene_symbol":"RNU6-1317P","gene_name":"RNA, U6 small nuclear 1317, pseudogene [Source:HGNC Symbol;Acc:HGNC:48280]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481596","summary":null,"start":175767558,"end":175767661,"strand":1,"description":"RNA, U6 small nuclear 1317, pseudogene [Source:HGNC Symbol;Acc:HGNC:48280]"}, {"versioned_ensembl_gene_id":"ENSG00000276656.1","gene_symbol":"MIR6083","gene_name":"microRNA 6083 [Source:HGNC Symbol;Acc:HGNC:50076]","synonyms":"hsa-mir-6083","biotype":"miRNA","ncbi_id":"102464832","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124374332,"end":124374437,"strand":1,"description":"microRNA 6083 [Source:HGNC Symbol;Acc:HGNC:50076]"}, {"versioned_ensembl_gene_id":"ENSG00000199145.1","gene_symbol":"MIR302D","gene_name":"microRNA 302d [Source:HGNC Symbol;Acc:HGNC:31765]","synonyms":"MIRN302D,hsa-mir-302d","biotype":"miRNA","ncbi_id":"442896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112648004,"end":112648071,"strand":-1,"description":"microRNA 302d [Source:HGNC Symbol;Acc:HGNC:31765]"}, {"versioned_ensembl_gene_id":"ENSG00000243591.3","gene_symbol":"RN7SL282P","gene_name":"RNA, 7SL, cytoplasmic 282, pseudogene [Source:HGNC Symbol;Acc:HGNC:46298]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480374","summary":null,"start":6601540,"end":6601836,"strand":1,"description":"RNA, 7SL, cytoplasmic 282, pseudogene [Source:HGNC Symbol;Acc:HGNC:46298]"}, {"versioned_ensembl_gene_id":"ENSG00000202186.1","gene_symbol":"RNU6-497P","gene_name":"RNA, U6 small nuclear 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:47460]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479786","summary":null,"start":47484278,"end":47484381,"strand":-1,"description":"RNA, U6 small nuclear 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:47460]"}, {"versioned_ensembl_gene_id":"ENSG00000265432.1","gene_symbol":"MIR4308","gene_name":"microRNA 4308 [Source:HGNC Symbol;Acc:HGNC:38206]","synonyms":"hsa-mir-4308","biotype":"miRNA","ncbi_id":"100422984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54878113,"end":54878193,"strand":-1,"description":"microRNA 4308 [Source:HGNC Symbol;Acc:HGNC:38206]"}, {"versioned_ensembl_gene_id":"ENSG00000265462.1","gene_symbol":"MIR3680-1","gene_name":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]","synonyms":"MIR3680,hsa-mir-3680","biotype":"miRNA","ncbi_id":"100500917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21506049,"end":21506135,"strand":-1,"description":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]"}, {"versioned_ensembl_gene_id":"ENSG00000280404.1","gene_symbol":"AC005086.4","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":102161120,"end":102161337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252581.1","gene_symbol":"RNU6-1098P","gene_name":"RNA, U6 small nuclear 1098, pseudogene [Source:HGNC Symbol;Acc:HGNC:48061]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481935","summary":null,"start":149525631,"end":149525726,"strand":1,"description":"RNA, U6 small nuclear 1098, pseudogene [Source:HGNC Symbol;Acc:HGNC:48061]"}, {"versioned_ensembl_gene_id":"ENSG00000252671.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10337277,"end":10337386,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278673.1","gene_symbol":"AC136352.5","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":20741,"end":22392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199626.1","gene_symbol":"RNU6-989P","gene_name":"RNA, U6 small nuclear 989, pseudogene [Source:HGNC Symbol;Acc:HGNC:47952]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481492","summary":null,"start":187270698,"end":187270804,"strand":-1,"description":"RNA, U6 small nuclear 989, pseudogene [Source:HGNC Symbol;Acc:HGNC:47952]"}, {"versioned_ensembl_gene_id":"ENSG00000265388.2","gene_symbol":"RN7SL391P","gene_name":"RNA, 7SL, cytoplasmic 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:46407]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481030","summary":null,"start":6344554,"end":6344837,"strand":1,"description":"RNA, 7SL, cytoplasmic 391, pseudogene [Source:HGNC Symbol;Acc:HGNC:46407]"}, {"versioned_ensembl_gene_id":"ENSG00000252141.1","gene_symbol":"RNU6-65P","gene_name":"RNA, U6 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:42555]","synonyms":"RNU6-65","biotype":"snRNA","ncbi_id":"106480751","summary":null,"start":51565412,"end":51565509,"strand":1,"description":"RNA, U6 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:42555]"}, {"versioned_ensembl_gene_id":"ENSG00000276690.1","gene_symbol":"SOX2OT_exon3","gene_name":"SOX2 overlapping transcript exon 3 [Source:RFAM;Acc:RF01953]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":181699608,"end":181699883,"strand":1,"description":"SOX2 overlapping transcript exon 3 [Source:RFAM;Acc:RF01953]"}, {"versioned_ensembl_gene_id":"ENSG00000240306.2","gene_symbol":"RN7SL100P","gene_name":"RNA, 7SL, cytoplasmic 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:46116]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480948","summary":null,"start":26895678,"end":26895970,"strand":1,"description":"RNA, 7SL, cytoplasmic 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:46116]"}, {"versioned_ensembl_gene_id":"ENSG00000238610.1","gene_symbol":"RNU7-26P","gene_name":"RNA, U7 small nuclear 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:34122]","synonyms":"U7.26","biotype":"snRNA","ncbi_id":"100147813","summary":null,"start":27897504,"end":27897566,"strand":-1,"description":"RNA, U7 small nuclear 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:34122]"}, {"versioned_ensembl_gene_id":"ENSG00000223262.1","gene_symbol":"RNA5SP492","gene_name":"RNA, 5S ribosomal pseudogene 492 [Source:HGNC Symbol;Acc:HGNC:43392]","synonyms":"RN5S492","biotype":"rRNA","ncbi_id":"100873734","summary":null,"start":42221173,"end":42221286,"strand":1,"description":"RNA, 5S ribosomal pseudogene 492 [Source:HGNC Symbol;Acc:HGNC:43392]"}, {"versioned_ensembl_gene_id":"ENSG00000274701.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":94655911,"end":94656208,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253079.1","gene_symbol":"NRON","gene_name":"non-protein coding RNA, repressor of NFAT [Source:HGNC Symbol;Acc:HGNC:37079]","synonyms":"NCRNA00194","biotype":"misc_RNA","ncbi_id":"641373","summary":null,"start":126408041,"end":126408410,"strand":-1,"description":"non-protein coding RNA, repressor of NFAT [Source:HGNC Symbol;Acc:HGNC:37079]"}, {"versioned_ensembl_gene_id":"ENSG00000252461.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":28881480,"end":28881607,"strand":-1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000276159.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000252821.1","gene_symbol":"RNU6-388P","gene_name":"RNA, U6 small nuclear 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:47351]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479737","summary":null,"start":33001950,"end":33002054,"strand":-1,"description":"RNA, U6 small nuclear 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:47351]"}, {"versioned_ensembl_gene_id":"ENSG00000206633.1","gene_symbol":"SNORA80B","gene_name":"small nucleolar RNA, H/ACA box 80B [Source:HGNC Symbol;Acc:HGNC:34355]","synonyms":"ACA67B","biotype":"snoRNA","ncbi_id":"100302743","summary":null,"start":10446714,"end":10446849,"strand":-1,"description":"small nucleolar RNA, H/ACA box 80B [Source:HGNC Symbol;Acc:HGNC:34355]"}, {"versioned_ensembl_gene_id":"ENSG00000199910.1","gene_symbol":"RNA5S10","gene_name":"RNA, 5S ribosomal 10 [Source:HGNC Symbol;Acc:HGNC:34371]","synonyms":"RN5S10","biotype":"rRNA","ncbi_id":"100169761","summary":null,"start":228630390,"end":228630508,"strand":-1,"description":"RNA, 5S ribosomal 10 [Source:HGNC Symbol;Acc:HGNC:34371]"}, {"versioned_ensembl_gene_id":"ENSG00000206845.1","gene_symbol":"RNU6-209P","gene_name":"RNA, U6 small nuclear 209, pseudogene [Source:HGNC 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[Source:HGNC Symbol;Acc:HGNC:46919]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480541","summary":null,"start":22130603,"end":22130729,"strand":-1,"description":"RNA, U6atac small nuclear 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46919]"}, {"versioned_ensembl_gene_id":"ENSG00000202476.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30453997,"end":30454097,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201483.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7187582,"end":7187686,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239333.3","gene_symbol":"RN7SL658P","gene_name":"RNA, 7SL, cytoplasmic 658, pseudogene [Source:HGNC 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Symbol;Acc:HGNC:50065]","synonyms":"hsa-mir-6887","biotype":"miRNA","ncbi_id":"102466205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35122700,"end":35122764,"strand":1,"description":"microRNA 6887 [Source:HGNC Symbol;Acc:HGNC:50065]"}, {"versioned_ensembl_gene_id":"ENSG00000265178.1","gene_symbol":"MIR4728","gene_name":"microRNA 4728 [Source:HGNC Symbol;Acc:HGNC:41632]","synonyms":"hsa-mir-4728","biotype":"miRNA","ncbi_id":"100616132","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39726495,"end":39726561,"strand":1,"description":"microRNA 4728 [Source:HGNC Symbol;Acc:HGNC:41632]"}, {"versioned_ensembl_gene_id":"ENSG00000274796.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,SEN34L,LENG5,LENG5,SEN34,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000278190.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868050,"end":54868156,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283454.1","gene_symbol":"RNA5SP443","gene_name":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]","synonyms":"RN5S443","biotype":"rRNA","ncbi_id":"106481745","summary":null,"start":45327366,"end":45327497,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]"}, {"versioned_ensembl_gene_id":"ENSG00000221255.1","gene_symbol":"RNU6ATAC37P","gene_name":"RNA, U6atac small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46936]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479558","summary":null,"start":7576841,"end":7576971,"strand":1,"description":"RNA, U6atac small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46936]"}, {"versioned_ensembl_gene_id":"ENSG00000200785.1","gene_symbol":"SNORD8","gene_name":"small nucleolar RNA, C/D box 8 [Source:HGNC Symbol;Acc:HGNC:20159]","synonyms":"RNU6C,mgU6-53","biotype":"snoRNA","ncbi_id":"319103","summary":null,"start":21397292,"end":21397401,"strand":-1,"description":"small nucleolar RNA, C/D box 8 [Source:HGNC Symbol;Acc:HGNC:20159]"}, {"versioned_ensembl_gene_id":"ENSG00000280466.1","gene_symbol":"SCARNA4","gene_name":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]","synonyms":"ACA26,ACA26","biotype":"scaRNA","ncbi_id":"677771","summary":null,"start":155925958,"end":155926085,"strand":-1,"description":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]"}, {"versioned_ensembl_gene_id":"ENSG00000201499.1","gene_symbol":"RNU6-312P","gene_name":"RNA, U6 small nuclear 312, pseudogene [Source:HGNC Symbol;Acc:HGNC:47275]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479706","summary":null,"start":200881715,"end":200881821,"strand":-1,"description":"RNA, U6 small nuclear 312, pseudogene [Source:HGNC Symbol;Acc:HGNC:47275]"}, {"versioned_ensembl_gene_id":"ENSG00000272296.1","gene_symbol":"SNORD96A","gene_name":"small nucleolar RNA, C/D box 96A [Source:HGNC Symbol;Acc:HGNC:32758]","synonyms":"U96a","biotype":"snoRNA","ncbi_id":"619571","summary":null,"start":181241814,"end":181241892,"strand":-1,"description":"small nucleolar RNA, C/D box 96A [Source:HGNC Symbol;Acc:HGNC:32758]"}, {"versioned_ensembl_gene_id":"ENSG00000275796.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PYPAF2,NBS1,CLR19.9,FLJ20510,NBS1,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54636119,"end":54671975,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000266875.2","gene_symbol":"RN7SL408P","gene_name":"RNA, 7SL, cytoplasmic 408, pseudogene [Source:HGNC Symbol;Acc:HGNC:46424]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481841","summary":null,"start":134133573,"end":134133868,"strand":1,"description":"RNA, 7SL, cytoplasmic 408, pseudogene [Source:HGNC Symbol;Acc:HGNC:46424]"}, {"versioned_ensembl_gene_id":"ENSG00000266059.2","gene_symbol":"RN7SL140P","gene_name":"RNA, 7SL, cytoplasmic 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:46156]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479272","summary":null,"start":20175346,"end":20175639,"strand":1,"description":"RNA, 7SL, cytoplasmic 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:46156]"}, {"versioned_ensembl_gene_id":"ENSG00000222650.1","gene_symbol":"RNU2-70P","gene_name":"RNA, U2 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:48563]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480227","summary":null,"start":236267780,"end":236267958,"strand":1,"description":"RNA, U2 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:48563]"}, {"versioned_ensembl_gene_id":"ENSG00000206963.1","gene_symbol":"RNU6-675P","gene_name":"RNA, U6 small nuclear 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:47638]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479864","summary":null,"start":126702839,"end":126702942,"strand":-1,"description":"RNA, U6 small nuclear 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:47638]"}, {"versioned_ensembl_gene_id":"ENSG00000200267.1","gene_symbol":"RNU6-66P","gene_name":"RNA, U6 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:42556]","synonyms":"RNU6-66","biotype":"snRNA","ncbi_id":"100873770","summary":null,"start":73112915,"end":73113018,"strand":-1,"description":"RNA, U6 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:42556]"}, {"versioned_ensembl_gene_id":"ENSG00000222385.1","gene_symbol":"RN7SKP158","gene_name":"RNA, 7SK small nuclear pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:45882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480883","summary":null,"start":28261194,"end":28261519,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:45882]"}, {"versioned_ensembl_gene_id":"ENSG00000201121.1","gene_symbol":"RNY1P12","gene_name":"RNA, Ro-associated Y1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50875]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480309","summary":null,"start":101662060,"end":101662164,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50875]"}, {"versioned_ensembl_gene_id":"ENSG00000199927.2","gene_symbol":"ACEA_U3","gene_name":"ACEA small nucleolar RNA U3 [Source:RFAM;Acc:RF01848]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30304320,"end":30304536,"strand":-1,"description":"ACEA small nucleolar RNA U3 [Source:RFAM;Acc:RF01848]"}, {"versioned_ensembl_gene_id":"ENSG00000272460.1","gene_symbol":"SNORD115-40","gene_name":"small nucleolar RNA, C/D box 115-40 [Source:HGNC Symbol;Acc:HGNC:33059]","synonyms":"HBII-52-40","biotype":"snoRNA","ncbi_id":"100033814","summary":null,"start":25243614,"end":25243695,"strand":1,"description":"small nucleolar RNA, C/D box 115-40 [Source:HGNC Symbol;Acc:HGNC:33059]"}, {"versioned_ensembl_gene_id":"ENSG00000263414.1","gene_symbol":"MIR3187","gene_name":"microRNA 3187 [Source:HGNC Symbol;Acc:HGNC:38319]","synonyms":"hsa-mir-3187","biotype":"miRNA","ncbi_id":"100422854","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":813584,"end":813653,"strand":1,"description":"microRNA 3187 [Source:HGNC Symbol;Acc:HGNC:38319]"}, {"versioned_ensembl_gene_id":"ENSG00000281552.1","gene_symbol":"AL035414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210303684,"end":210304540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000208022.1","gene_symbol":"MIR618","gene_name":"microRNA 618 [Source:HGNC Symbol;Acc:HGNC:32874]","synonyms":"MIRN618,hsa-mir-618","biotype":"miRNA","ncbi_id":"693203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80935736,"end":80935833,"strand":-1,"description":"microRNA 618 [Source:HGNC Symbol;Acc:HGNC:32874]"}, {"versioned_ensembl_gene_id":"ENSG00000284259.1","gene_symbol":"MIR6773","gene_name":"microRNA 6773 [Source:HGNC Symbol;Acc:HGNC:50132]","synonyms":"hsa-mir-6773","biotype":"miRNA","ncbi_id":"102466194","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68233426,"end":68233499,"strand":-1,"description":"microRNA 6773 [Source:HGNC Symbol;Acc:HGNC:50132]"}, {"versioned_ensembl_gene_id":"ENSG00000263584.1","gene_symbol":"MIR4480","gene_name":"microRNA 4480 [Source:HGNC Symbol;Acc:HGNC:41716]","synonyms":"hsa-mir-4480","biotype":"miRNA","ncbi_id":"100616151","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12578753,"end":12578823,"strand":1,"description":"microRNA 4480 [Source:HGNC Symbol;Acc:HGNC:41716]"}, {"versioned_ensembl_gene_id":"ENSG00000251842.1","gene_symbol":"RNU6-732P","gene_name":"RNA, U6 small nuclear 732, pseudogene [Source:HGNC Symbol;Acc:HGNC:47695]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479890","summary":null,"start":149057554,"end":149057656,"strand":-1,"description":"RNA, U6 small nuclear 732, pseudogene [Source:HGNC Symbol;Acc:HGNC:47695]"}, {"versioned_ensembl_gene_id":"ENSG00000252772.1","gene_symbol":"RNU6-714P","gene_name":"RNA, U6 small nuclear 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:47677]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480603","summary":null,"start":92820977,"end":92821079,"strand":1,"description":"RNA, U6 small nuclear 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:47677]"}, {"versioned_ensembl_gene_id":"ENSG00000265048.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32360267,"end":32360373,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201342.1","gene_symbol":"RNU4-38P","gene_name":"RNA, U4 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46974]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479574","summary":null,"start":170057301,"end":170057429,"strand":1,"description":"RNA, U4 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:46974]"}, {"versioned_ensembl_gene_id":"ENSG00000251893.2","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":75689152,"end":75689304,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000283584.1","gene_symbol":"snoMe28S-Am2634","gene_name":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":7431217,"end":7431296,"strand":1,"description":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]"}, {"versioned_ensembl_gene_id":"ENSG00000253043.1","gene_symbol":"RNU7-181P","gene_name":"RNA, U7 small nuclear 181 pseudogene [Source:HGNC Symbol;Acc:HGNC:45715]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479093","summary":null,"start":130004528,"end":130004601,"strand":-1,"description":"RNA, U7 small nuclear 181 pseudogene [Source:HGNC Symbol;Acc:HGNC:45715]"}, {"versioned_ensembl_gene_id":"ENSG00000222114.1","gene_symbol":"RNU6-985P","gene_name":"RNA, U6 small nuclear 985, pseudogene [Source:HGNC Symbol;Acc:HGNC:47948]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480001","summary":null,"start":137687891,"end":137687994,"strand":-1,"description":"RNA, U6 small nuclear 985, pseudogene [Source:HGNC Symbol;Acc:HGNC:47948]"}, {"versioned_ensembl_gene_id":"ENSG00000206999.1","gene_symbol":"RNU6-622P","gene_name":"RNA, U6 small nuclear 622, pseudogene [Source:HGNC Symbol;Acc:HGNC:47585]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479841","summary":null,"start":75183045,"end":75183147,"strand":1,"description":"RNA, U6 small nuclear 622, pseudogene [Source:HGNC Symbol;Acc:HGNC:47585]"}, {"versioned_ensembl_gene_id":"ENSG00000275133.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30050669,"end":30050772,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000240374.3","gene_symbol":"RN7SL503P","gene_name":"RNA, 7SL, cytoplasmic 503, pseudogene [Source:HGNC Symbol;Acc:HGNC:46519]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481060","summary":null,"start":35292196,"end":35292498,"strand":-1,"description":"RNA, 7SL, cytoplasmic 503, pseudogene [Source:HGNC Symbol;Acc:HGNC:46519]"}, {"versioned_ensembl_gene_id":"ENSG00000281917.2","gene_symbol":"SLC16A1","gene_name":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]","synonyms":"MCT1,MCT","biotype":"protein_coding","ncbi_id":"6566","summary":"The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]","start":112911847,"end":112957013,"strand":-1,"description":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]"}, {"versioned_ensembl_gene_id":"ENSG00000218227.3","gene_symbol":"AC136632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178055604,"end":178056194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273945.1","gene_symbol":"MIR6853","gene_name":"microRNA 6853 [Source:HGNC Symbol;Acc:HGNC:49945]","synonyms":"hsa-mir-6853","biotype":"miRNA","ncbi_id":"102466201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35732922,"end":35732995,"strand":1,"description":"microRNA 6853 [Source:HGNC Symbol;Acc:HGNC:49945]"}, {"versioned_ensembl_gene_id":"ENSG00000283369.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":247607126,"end":247607201,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000253054.1","gene_symbol":"RNU7-77P","gene_name":"RNA, U7 small nuclear 77 pseudogene [Source:HGNC Symbol;Acc:HGNC:34173]","synonyms":"U7.77","biotype":"snRNA","ncbi_id":"100151674","summary":null,"start":35135443,"end":35135502,"strand":1,"description":"RNA, U7 small nuclear 77 pseudogene [Source:HGNC Symbol;Acc:HGNC:34173]"}, {"versioned_ensembl_gene_id":"ENSG00000251925.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":23423099,"end":23423236,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000264389.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32485042,"end":32485188,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000200794.1","gene_symbol":"RN7SKP250","gene_name":"RNA, 7SK small nuclear pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:45974]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479206","summary":null,"start":109662863,"end":109663183,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:45974]"}, {"versioned_ensembl_gene_id":"ENSG00000201569.1","gene_symbol":"SNORD114-17","gene_name":"small nucleolar RNA, C/D box 114-17 [Source:HGNC Symbol;Acc:HGNC:33005]","synonyms":"14q(II-17)","biotype":"snoRNA","ncbi_id":"767595","summary":null,"start":100974806,"end":100974880,"strand":1,"description":"small nucleolar RNA, C/D box 114-17 [Source:HGNC Symbol;Acc:HGNC:33005]"}, {"versioned_ensembl_gene_id":"ENSG00000200152.1","gene_symbol":"RNU6-216P","gene_name":"RNA, U6 small nuclear 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:47179]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479662","summary":null,"start":74968189,"end":74968292,"strand":-1,"description":"RNA, U6 small nuclear 216, pseudogene [Source:HGNC Symbol;Acc:HGNC:47179]"}, {"versioned_ensembl_gene_id":"ENSG00000200303.1","gene_symbol":"RNU6-940P","gene_name":"RNA, U6 small nuclear 940, pseudogene [Source:HGNC Symbol;Acc:HGNC:47903]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479982","summary":null,"start":48975543,"end":48975646,"strand":1,"description":"RNA, U6 small nuclear 940, pseudogene [Source:HGNC Symbol;Acc:HGNC:47903]"}, {"versioned_ensembl_gene_id":"ENSG00000199150.3","gene_symbol":"MIRLET7G","gene_name":"microRNA let-7g [Source:HGNC Symbol;Acc:HGNC:31485]","synonyms":"MIRNLET7G,hsa-let-7g","biotype":"miRNA","ncbi_id":"406890","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52268278,"end":52268361,"strand":-1,"description":"microRNA let-7g [Source:HGNC Symbol;Acc:HGNC:31485]"}, {"versioned_ensembl_gene_id":"ENSG00000253075.1","gene_symbol":"RN7SKP92","gene_name":"RNA, 7SK small nuclear pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:45816]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479135","summary":null,"start":100487544,"end":100487787,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:45816]"}, {"versioned_ensembl_gene_id":"ENSG00000273570.1","gene_symbol":"RMST_5","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 5 [Source:RFAM;Acc:RF01966]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97495932,"end":97496057,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 5 [Source:RFAM;Acc:RF01966]"}, {"versioned_ensembl_gene_id":"ENSG00000280968.1","gene_symbol":"MIR3653","gene_name":"microRNA 3653 [Source:HGNC Symbol;Acc:HGNC:38971]","synonyms":"hsa-mir-3653","biotype":"miRNA","ncbi_id":"100500833","summary":"This record was withdrawn by miRBase.","start":29333158,"end":29333267,"strand":-1,"description":"microRNA 3653 [Source:HGNC Symbol;Acc:HGNC:38971]"}, {"versioned_ensembl_gene_id":"ENSG00000207626.1","gene_symbol":"MIR562","gene_name":"microRNA 562 [Source:HGNC Symbol;Acc:HGNC:32818]","synonyms":"hsa-mir-562,MIRN562","biotype":"miRNA","ncbi_id":"693147","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":232172653,"end":232172747,"strand":1,"description":"microRNA 562 [Source:HGNC Symbol;Acc:HGNC:32818]"}, {"versioned_ensembl_gene_id":"ENSG00000222644.1","gene_symbol":"RNU2-16P","gene_name":"RNA, U2 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:48509]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481639","summary":null,"start":75829454,"end":75829589,"strand":-1,"description":"RNA, U2 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:48509]"}, {"versioned_ensembl_gene_id":"ENSG00000265156.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"U52,RNU52,U52,RNU52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31827320,"end":31827386,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000263764.1","gene_symbol":"SNORD43","gene_name":"small nucleolar RNA, C/D box 43 [Source:HGNC Symbol;Acc:HGNC:10182]","synonyms":"U43,RNU43","biotype":"snoRNA","ncbi_id":"26807","summary":"Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD43, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD43, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]","start":39319050,"end":39319113,"strand":-1,"description":"small nucleolar RNA, C/D box 43 [Source:HGNC Symbol;Acc:HGNC:10182]"}, {"versioned_ensembl_gene_id":"ENSG00000239868.3","gene_symbol":"RN7SL34P","gene_name":"RNA, 7SL, cytoplasmic 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46050]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481824","summary":null,"start":41286424,"end":41286693,"strand":-1,"description":"RNA, 7SL, cytoplasmic 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46050]"}, {"versioned_ensembl_gene_id":"ENSG00000199525.1","gene_symbol":"RNA5SP295","gene_name":"RNA, 5S ribosomal pseudogene 295 [Source:HGNC Symbol;Acc:HGNC:43195]","synonyms":"RN5S295","biotype":"rRNA","ncbi_id":"100873548","summary":null,"start":112252258,"end":112252378,"strand":1,"description":"RNA, 5S ribosomal pseudogene 295 [Source:HGNC Symbol;Acc:HGNC:43195]"}, {"versioned_ensembl_gene_id":"ENSG00000222858.1","gene_symbol":"RNU6-920P","gene_name":"RNA, U6 small nuclear 920, pseudogene [Source:HGNC Symbol;Acc:HGNC:47883]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481470","summary":null,"start":29641611,"end":29641702,"strand":-1,"description":"RNA, U6 small nuclear 920, pseudogene [Source:HGNC Symbol;Acc:HGNC:47883]"}, {"versioned_ensembl_gene_id":"ENSG00000234428.2","gene_symbol":"AC023051.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26623369,"end":26649479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207620.1","gene_symbol":"MIR516A2","gene_name":"microRNA 516a-2 [Source:HGNC Symbol;Acc:HGNC:32131]","synonyms":"MIRN516A2,MIRN516-2,hsa-mir-516a-2,hsa-mir-516-2","biotype":"miRNA","ncbi_id":"574499","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53761133,"end":53761222,"strand":1,"description":"microRNA 516a-2 [Source:HGNC Symbol;Acc:HGNC:32131]"}, {"versioned_ensembl_gene_id":"ENSG00000252859.1","gene_symbol":"RNU6-375P","gene_name":"RNA, U6 small nuclear 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:47338]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480575","summary":null,"start":41168217,"end":41168316,"strand":1,"description":"RNA, U6 small nuclear 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:47338]"}, {"versioned_ensembl_gene_id":"ENSG00000252087.1","gene_symbol":"RN7SKP248","gene_name":"RNA, 7SK small nuclear pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:45972]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480476","summary":null,"start":90370123,"end":90370427,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:45972]"}, {"versioned_ensembl_gene_id":"ENSG00000207730.3","gene_symbol":"MIR200B","gene_name":"microRNA 200b [Source:HGNC Symbol;Acc:HGNC:31579]","synonyms":"MIRN200B,hsa-mir-200b","biotype":"miRNA","ncbi_id":"406984","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1167104,"end":1167198,"strand":1,"description":"microRNA 200b [Source:HGNC Symbol;Acc:HGNC:31579]"}, {"versioned_ensembl_gene_id":"ENSG00000207868.1","gene_symbol":"MIR514A1","gene_name":"microRNA 514a-1 [Source:HGNC Symbol;Acc:HGNC:32148]","synonyms":"MIRN514-1,MIR514-1,hsa-mir-514-1","biotype":"miRNA","ncbi_id":"574516","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147279247,"end":147279344,"strand":-1,"description":"microRNA 514a-1 [Source:HGNC Symbol;Acc:HGNC:32148]"}, {"versioned_ensembl_gene_id":"ENSG00000240767.3","gene_symbol":"RN7SL288P","gene_name":"RNA, 7SL, cytoplasmic 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:46304]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481000","summary":null,"start":46169458,"end":46169748,"strand":-1,"description":"RNA, 7SL, cytoplasmic 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:46304]"}, {"versioned_ensembl_gene_id":"ENSG00000283210.1","gene_symbol":"MIR1322","gene_name":"microRNA 1322 [Source:HGNC Symbol;Acc:HGNC:35374]","synonyms":"MIRN1322,hsa-mir-1322","biotype":"miRNA","ncbi_id":"100302166","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10825373,"end":10825443,"strand":-1,"description":"microRNA 1322 [Source:HGNC Symbol;Acc:HGNC:35374]"}, {"versioned_ensembl_gene_id":"ENSG00000283289.1","gene_symbol":"MIR524","gene_name":"microRNA 524 [Source:HGNC Symbol;Acc:HGNC:32110]","synonyms":"MIRN524,hsa-mir-524","biotype":"miRNA","ncbi_id":"574478","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53711002,"end":53711088,"strand":1,"description":"microRNA 524 [Source:HGNC Symbol;Acc:HGNC:32110]"}, {"versioned_ensembl_gene_id":"ENSG00000264292.1","gene_symbol":"MIR2467","gene_name":"microRNA 2467 [Source:HGNC Symbol;Acc:HGNC:41881]","synonyms":"hsa-mir-2467","biotype":"miRNA","ncbi_id":"100616360","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239351724,"end":239351804,"strand":-1,"description":"microRNA 2467 [Source:HGNC Symbol;Acc:HGNC:41881]"}, {"versioned_ensembl_gene_id":"ENSG00000256894.1","gene_symbol":"AC022509.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26125155,"end":26126617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284375.1","gene_symbol":"MIR19B1","gene_name":"microRNA 19b-1 [Source:HGNC Symbol;Acc:HGNC:31575]","synonyms":"MIRN19B1,hsa-mir-19b-1","biotype":"miRNA","ncbi_id":"406980","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91351192,"end":91351278,"strand":1,"description":"microRNA 19b-1 [Source:HGNC Symbol;Acc:HGNC:31575]"}, {"versioned_ensembl_gene_id":"ENSG00000283532.1","gene_symbol":"MIR4317","gene_name":"microRNA 4317 [Source:HGNC Symbol;Acc:HGNC:38260]","synonyms":"hsa-mir-4317","biotype":"miRNA","ncbi_id":"100422840","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6374361,"end":6374425,"strand":-1,"description":"microRNA 4317 [Source:HGNC Symbol;Acc:HGNC:38260]"}, {"versioned_ensembl_gene_id":"ENSG00000266370.1","gene_symbol":"MIR3657","gene_name":"microRNA 3657 [Source:HGNC Symbol;Acc:HGNC:38906]","synonyms":"hsa-mir-3657","biotype":"miRNA","ncbi_id":"100500889","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112037599,"end":112037715,"strand":-1,"description":"microRNA 3657 [Source:HGNC Symbol;Acc:HGNC:38906]"}, {"versioned_ensembl_gene_id":"ENSG00000200650.1","gene_symbol":"RNA5SP114","gene_name":"RNA, 5S ribosomal pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:42912]","synonyms":"RN5S114","biotype":"rRNA","ncbi_id":"100873384","summary":null,"start":188276732,"end":188276844,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:42912]"}, {"versioned_ensembl_gene_id":"ENSG00000200714.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65592731,"end":65592820,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281185.1","gene_symbol":"GPX6","gene_name":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]","synonyms":"GPXP3,GPXP3","biotype":"protein_coding","ncbi_id":"257202","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. Expression of this gene has been observed in embryos and olfactory epithelium; however, the exact function of this gene is not known. This isozyme is a selenoprotein in humans, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. The orthologs of this gene in mouse and rat (and some other species) contain a cysteine (Cys) residue in place of the Sec residue, and their corresponding mRNAs lack SECIS element. [provided by RefSeq, Jul 2017]","start":28510773,"end":28515743,"strand":-1,"description":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]"}, {"versioned_ensembl_gene_id":"ENSG00000202445.1","gene_symbol":"RNU6-669P","gene_name":"RNA, U6 small nuclear 669, pseudogene [Source:HGNC Symbol;Acc:HGNC:47632]","synonyms":null,"biotype":"snRNA","ncbi_id":"107063537","summary":null,"start":94507738,"end":94507844,"strand":1,"description":"RNA, U6 small nuclear 669, pseudogene [Source:HGNC Symbol;Acc:HGNC:47632]"}, {"versioned_ensembl_gene_id":"ENSG00000238963.2","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":154905076,"end":154905206,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000252506.1","gene_symbol":"RNU6-180P","gene_name":"RNA, U6 small nuclear 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:47143]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481233","summary":null,"start":229383128,"end":229383188,"strand":1,"description":"RNA, U6 small nuclear 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:47143]"}, {"versioned_ensembl_gene_id":"ENSG00000277584.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":190019116,"end":190019233,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222383.1","gene_symbol":"RNA5SP203","gene_name":"RNA, 5S ribosomal pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:43103]","synonyms":"RN5S203","biotype":"rRNA","ncbi_id":"100873464","summary":null,"start":10752791,"end":10752926,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:43103]"}, {"versioned_ensembl_gene_id":"ENSG00000277678.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":145169519,"end":145169664,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000252222.1","gene_symbol":"RNU7-13P","gene_name":"RNA, U7 small nuclear 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:34109]","synonyms":"U7.13","biotype":"snRNA","ncbi_id":"100147761","summary":null,"start":184821428,"end":184821489,"strand":-1,"description":"RNA, U7 small nuclear 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:34109]"}, {"versioned_ensembl_gene_id":"ENSG00000264438.2","gene_symbol":"RN7SL560P","gene_name":"RNA, 7SL, cytoplasmic 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:46576]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479426","summary":null,"start":128709780,"end":128710043,"strand":1,"description":"RNA, 7SL, cytoplasmic 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:46576]"}, {"versioned_ensembl_gene_id":"ENSG00000251851.1","gene_symbol":"RNU6-772P","gene_name":"RNA, U6 small nuclear 772, pseudogene [Source:HGNC Symbol;Acc:HGNC:47735]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479908","summary":null,"start":20355748,"end":20355852,"strand":-1,"description":"RNA, U6 small nuclear 772, pseudogene [Source:HGNC Symbol;Acc:HGNC:47735]"}, {"versioned_ensembl_gene_id":"ENSG00000252452.1","gene_symbol":"RNU6-107P","gene_name":"RNA, U6 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:47070]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479614","summary":null,"start":232782665,"end":232782766,"strand":1,"description":"RNA, U6 small nuclear 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:47070]"}, {"versioned_ensembl_gene_id":"ENSG00000221719.1","gene_symbol":"SNORA3C","gene_name":"small nucleolar RNA, H/ACA box 3C [Source:HGNC Symbol;Acc:HGNC:52203]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616997","summary":null,"start":2796408,"end":2796532,"strand":-1,"description":"small nucleolar RNA, H/ACA box 3C [Source:HGNC Symbol;Acc:HGNC:52203]"}, {"versioned_ensembl_gene_id":"ENSG00000243801.3","gene_symbol":"RN7SL461P","gene_name":"RNA, 7SL, cytoplasmic 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:46477]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481844","summary":null,"start":56824375,"end":56824656,"strand":-1,"description":"RNA, 7SL, cytoplasmic 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:46477]"}, {"versioned_ensembl_gene_id":"ENSG00000223951.1","gene_symbol":"AL133244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33056333,"end":33063113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276580.1","gene_symbol":"MIR8055","gene_name":"microRNA 8055 [Source:HGNC Symbol;Acc:HGNC:50241]","synonyms":"hsa-mir-8055","biotype":"miRNA","ncbi_id":"102465861","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6622124,"end":6622220,"strand":-1,"description":"microRNA 8055 [Source:HGNC Symbol;Acc:HGNC:50241]"}, {"versioned_ensembl_gene_id":"ENSG00000266750.1","gene_symbol":"MIR4645","gene_name":"microRNA 4645 [Source:HGNC Symbol;Acc:HGNC:41689]","synonyms":"hsa-mir-4645","biotype":"miRNA","ncbi_id":"100616285","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2854031,"end":2854107,"strand":-1,"description":"microRNA 4645 [Source:HGNC Symbol;Acc:HGNC:41689]"}, {"versioned_ensembl_gene_id":"ENSG00000200774.1","gene_symbol":"RNU6-478P","gene_name":"RNA, U6 small nuclear 478, pseudogene [Source:HGNC Symbol;Acc:HGNC:47441]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479778","summary":null,"start":83067962,"end":83068071,"strand":-1,"description":"RNA, U6 small nuclear 478, pseudogene [Source:HGNC Symbol;Acc:HGNC:47441]"}, {"versioned_ensembl_gene_id":"ENSG00000201487.1","gene_symbol":"SNORD45B","gene_name":"small nucleolar RNA, C/D box 45B [Source:HGNC Symbol;Acc:HGNC:10185]","synonyms":"U45b,RNU45B","biotype":"snoRNA","ncbi_id":"26804","summary":null,"start":75789477,"end":75789548,"strand":1,"description":"small nucleolar RNA, C/D box 45B [Source:HGNC Symbol;Acc:HGNC:10185]"}, {"versioned_ensembl_gene_id":"ENSG00000202368.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96979528,"end":96979629,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266119.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30726158,"end":30726268,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252137.1","gene_symbol":"RNU6-1338P","gene_name":"RNA, U6 small nuclear 1338, pseudogene [Source:HGNC Symbol;Acc:HGNC:48301]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480150","summary":null,"start":75593055,"end":75593145,"strand":1,"description":"RNA, U6 small nuclear 1338, pseudogene [Source:HGNC Symbol;Acc:HGNC:48301]"}, {"versioned_ensembl_gene_id":"ENSG00000199740.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50939927,"end":50940026,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276341.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55049943,"end":55068836,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000274321.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88520000,"end":88520170,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000239180.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":70311607,"end":70311701,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265260.2","gene_symbol":"RN7SL74P","gene_name":"RNA, 7SL, cytoplasmic 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:46090]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480942","summary":null,"start":97341046,"end":97341344,"strand":1,"description":"RNA, 7SL, cytoplasmic 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:46090]"}, {"versioned_ensembl_gene_id":"ENSG00000264462.1","gene_symbol":"MIR3648-2","gene_name":"microRNA 3648-2 [Source:HGNC Symbol;Acc:HGNC:50843]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504731","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8986999,"end":8987178,"strand":1,"description":"microRNA 3648-2 [Source:HGNC Symbol;Acc:HGNC:50843]"}, {"versioned_ensembl_gene_id":"ENSG00000207815.1","gene_symbol":"MIR563","gene_name":"microRNA 563 [Source:HGNC Symbol;Acc:HGNC:32819]","synonyms":"MIRN563,hsa-mir-563","biotype":"miRNA","ncbi_id":"693148","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15873771,"end":15873849,"strand":1,"description":"microRNA 563 [Source:HGNC Symbol;Acc:HGNC:32819]"}, {"versioned_ensembl_gene_id":"ENSG00000277707.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000200298.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72022407,"end":72022516,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240545.3","gene_symbol":"RN7SL492P","gene_name":"RNA, 7SL, cytoplasmic 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:46508]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479402","summary":null,"start":56794348,"end":56794642,"strand":-1,"description":"RNA, 7SL, cytoplasmic 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:46508]"}, {"versioned_ensembl_gene_id":"ENSG00000232058.1","gene_symbol":"AC005772.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15014805,"end":15052276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276169.1","gene_symbol":"MIR6871","gene_name":"microRNA 6871 [Source:HGNC Symbol;Acc:HGNC:49964]","synonyms":"hsa-mir-6871","biotype":"miRNA","ncbi_id":"102466912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41169023,"end":41169078,"strand":1,"description":"microRNA 6871 [Source:HGNC Symbol;Acc:HGNC:49964]"}, {"versioned_ensembl_gene_id":"ENSG00000199458.1","gene_symbol":"RNU4-35P","gene_name":"RNA, U4 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46971]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481182","summary":null,"start":121453981,"end":121454121,"strand":-1,"description":"RNA, U4 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46971]"}, {"versioned_ensembl_gene_id":"ENSG00000199839.1","gene_symbol":"RNA5SP150","gene_name":"RNA, 5S ribosomal pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:43050]","synonyms":"RN5S150","biotype":"rRNA","ncbi_id":"100873416","summary":null,"start":181822872,"end":181822990,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:43050]"}, {"versioned_ensembl_gene_id":"ENSG00000265537.1","gene_symbol":"MIR3180-1","gene_name":"microRNA 3180-1 [Source:HGNC Symbol;Acc:HGNC:38382]","synonyms":"hsa-mir-3180-1","biotype":"miRNA","ncbi_id":"100422870","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14911220,"end":14911313,"strand":1,"description":"microRNA 3180-1 [Source:HGNC Symbol;Acc:HGNC:38382]"}, {"versioned_ensembl_gene_id":"ENSG00000252411.1","gene_symbol":"RNU6-1087P","gene_name":"RNA, U6 small nuclear 1087, pseudogene [Source:HGNC Symbol;Acc:HGNC:48050]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481522","summary":null,"start":35594173,"end":35594273,"strand":1,"description":"RNA, U6 small nuclear 1087, pseudogene [Source:HGNC Symbol;Acc:HGNC:48050]"}, {"versioned_ensembl_gene_id":"ENSG00000277391.1","gene_symbol":"MIR6881","gene_name":"microRNA 6881 [Source:HGNC Symbol;Acc:HGNC:50098]","synonyms":"hsa-mir-6881","biotype":"miRNA","ncbi_id":"102465530","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74411357,"end":74411432,"strand":-1,"description":"microRNA 6881 [Source:HGNC Symbol;Acc:HGNC:50098]"}, {"versioned_ensembl_gene_id":"ENSG00000265612.1","gene_symbol":"MIR4539","gene_name":"microRNA 4539 [Source:HGNC Symbol;Acc:HGNC:41546]","synonyms":"hsa-mir-4539","biotype":"miRNA","ncbi_id":"100616374","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105857513,"end":105857572,"strand":-1,"description":"microRNA 4539 [Source:HGNC Symbol;Acc:HGNC:41546]"}, {"versioned_ensembl_gene_id":"ENSG00000252824.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":102194076,"end":102194164,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000265768.1","gene_symbol":"MIR4506","gene_name":"microRNA 4506 [Source:HGNC Symbol;Acc:HGNC:41663]","synonyms":"hsa-mir-4506","biotype":"miRNA","ncbi_id":"100616140","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93948226,"end":93948302,"strand":-1,"description":"microRNA 4506 [Source:HGNC Symbol;Acc:HGNC:41663]"}, {"versioned_ensembl_gene_id":"ENSG00000277739.1","gene_symbol":"RNA5-8SN1","gene_name":"RNA, 5.8S ribosomal N1 [Source:HGNC Symbol;Acc:HGNC:53517]","synonyms":null,"biotype":"rRNA","ncbi_id":"106632260","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units, that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. Gene and RefSeq, in collaboration with HGNC, currently describe one 45S rDNA cluster, and one set of 45S precursor and product rRNAs, for each of the five human chromosomes to which these loci are localized. This gene is a representative copy of the 5.8S ribosomal RNA on chromosome 21. [provided by RefSeq, Feb 2017]","start":8256781,"end":8256933,"strand":1,"description":"RNA, 5.8S ribosomal N1 [Source:HGNC Symbol;Acc:HGNC:53517]"}, {"versioned_ensembl_gene_id":"ENSG00000229012.1","gene_symbol":"AC003685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8863861,"end":8867601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237594.2","gene_symbol":"AP000251.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31559245,"end":31560487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283699.1","gene_symbol":"MIR4481","gene_name":"microRNA 4481 [Source:HGNC Symbol;Acc:HGNC:41781]","synonyms":"hsa-mir-4481","biotype":"miRNA","ncbi_id":"100616320","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12653138,"end":12653197,"strand":-1,"description":"microRNA 4481 [Source:HGNC Symbol;Acc:HGNC:41781]"}, {"versioned_ensembl_gene_id":"ENSG00000222747.1","gene_symbol":"RNA5SP25","gene_name":"RNA, 5S ribosomal pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42601]","synonyms":"RN5S25","biotype":"rRNA","ncbi_id":"100873357","summary":null,"start":21369790,"end":21369899,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42601]"}, {"versioned_ensembl_gene_id":"ENSG00000206797.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":450663,"end":450762,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264553.1","gene_symbol":"MIR4257","gene_name":"microRNA 4257 [Source:HGNC Symbol;Acc:HGNC:38312]","synonyms":"hsa-mir-4257","biotype":"miRNA","ncbi_id":"100422997","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":150551929,"end":150552014,"strand":1,"description":"microRNA 4257 [Source:HGNC Symbol;Acc:HGNC:38312]"}, {"versioned_ensembl_gene_id":"ENSG00000202386.1","gene_symbol":"RNA5SP211","gene_name":"RNA, 5S ribosomal pseudogene 211 [Source:HGNC Symbol;Acc:HGNC:43111]","synonyms":"RN5S211","biotype":"rRNA","ncbi_id":"100873471","summary":null,"start":106449381,"end":106449497,"strand":1,"description":"RNA, 5S ribosomal pseudogene 211 [Source:HGNC Symbol;Acc:HGNC:43111]"}, {"versioned_ensembl_gene_id":"ENSG00000265815.1","gene_symbol":"MIR1273G","gene_name":"microRNA 1273g [Source:HGNC Symbol;Acc:HGNC:41684]","synonyms":"hsa-mir-1273g","biotype":"miRNA","ncbi_id":"100616145","summary":"This record was withdrawn by miRBase.","start":52940314,"end":52940413,"strand":1,"description":"microRNA 1273g [Source:HGNC Symbol;Acc:HGNC:41684]"}, {"versioned_ensembl_gene_id":"ENSG00000283477.1","gene_symbol":"MIR6079","gene_name":"microRNA 6079 [Source:HGNC Symbol;Acc:HGNC:50114]","synonyms":"hsa-mir-6079","biotype":"miRNA","ncbi_id":"102464830","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43838622,"end":43838683,"strand":1,"description":"microRNA 6079 [Source:HGNC Symbol;Acc:HGNC:50114]"}, {"versioned_ensembl_gene_id":"ENSG00000199594.1","gene_symbol":"RNU6-1301P","gene_name":"RNA, U6 small nuclear 1301, pseudogene [Source:HGNC Symbol;Acc:HGNC:48264]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481591","summary":null,"start":37140327,"end":37140430,"strand":1,"description":"RNA, U6 small nuclear 1301, pseudogene [Source:HGNC Symbol;Acc:HGNC:48264]"}, {"versioned_ensembl_gene_id":"ENSG00000252587.1","gene_symbol":"RNA5SP422","gene_name":"RNA, 5S ribosomal pseudogene 422 [Source:HGNC Symbol;Acc:HGNC:43322]","synonyms":"RN5S422","biotype":"rRNA","ncbi_id":"100873673","summary":null,"start":35754923,"end":35755033,"strand":1,"description":"RNA, 5S ribosomal pseudogene 422 [Source:HGNC Symbol;Acc:HGNC:43322]"}, {"versioned_ensembl_gene_id":"ENSG00000221206.1","gene_symbol":"RNU6ATAC15P","gene_name":"RNA, U6atac small nuclear 15, 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{"versioned_ensembl_gene_id":"ENSG00000277637.1","gene_symbol":"RN7SL469P","gene_name":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480512","summary":null,"start":30143733,"end":30143969,"strand":1,"description":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]"}, {"versioned_ensembl_gene_id":"ENSG00000283509.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":129819777,"end":129819876,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000199668.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11315067,"end":11315178,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278457.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":380608,"end":380726,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000252147.1","gene_symbol":"RNY3P16","gene_name":"RNA, Ro-associated Y3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50891]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480686","summary":null,"start":119456558,"end":119456658,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50891]"}, {"versioned_ensembl_gene_id":"ENSG00000274408.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":146539541,"end":146539663,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000201660.1","gene_symbol":"SNORA20","gene_name":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":5410122,"end":5410251,"strand":1,"description":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]"}, {"versioned_ensembl_gene_id":"ENSG00000283675.1","gene_symbol":"snoMe28S-Am2634","gene_name":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":19420279,"end":19420342,"strand":1,"description":"Small nucleolar RNA Me28S-Am2634 [Source:RFAM;Acc:RF00537]"}, {"versioned_ensembl_gene_id":"ENSG00000199855.1","gene_symbol":"RNU6-490P","gene_name":"RNA, U6 small nuclear 490, pseudogene [Source:HGNC Symbol;Acc:HGNC:47453]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479783","summary":null,"start":27088321,"end":27088427,"strand":-1,"description":"RNA, U6 small nuclear 490, pseudogene [Source:HGNC Symbol;Acc:HGNC:47453]"}, {"versioned_ensembl_gene_id":"ENSG00000252530.1","gene_symbol":"RNU6-965P","gene_name":"RNA, U6 small nuclear 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:47928]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481484","summary":null,"start":101728642,"end":101728737,"strand":-1,"description":"RNA, U6 small nuclear 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:47928]"}, {"versioned_ensembl_gene_id":"ENSG00000238457.1","gene_symbol":"RNU7-169P","gene_name":"RNA, U7 small nuclear 169 pseudogene [Source:HGNC Symbol;Acc:HGNC:45703]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480827","summary":null,"start":108668448,"end":108668508,"strand":1,"description":"RNA, U7 small nuclear 169 pseudogene [Source:HGNC Symbol;Acc:HGNC:45703]"}, {"versioned_ensembl_gene_id":"ENSG00000237325.3","gene_symbol":"AP000563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31452466,"end":31453223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200105.1","gene_symbol":"RNU6-251P","gene_name":"RNA, U6 small nuclear 251, pseudogene [Source:HGNC Symbol;Acc:HGNC:47214]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481257","summary":null,"start":15671707,"end":15671810,"strand":-1,"description":"RNA, U6 small nuclear 251, pseudogene [Source:HGNC Symbol;Acc:HGNC:47214]"}, {"versioned_ensembl_gene_id":"ENSG00000212445.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":68189287,"end":68189421,"strand":1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000265584.1","gene_symbol":"MIR3978","gene_name":"microRNA 3978 [Source:HGNC Symbol;Acc:HGNC:41630]","synonyms":"hsa-mir-3978","biotype":"miRNA","ncbi_id":"100616491","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110082118,"end":110082218,"strand":1,"description":"microRNA 3978 [Source:HGNC Symbol;Acc:HGNC:41630]"}, {"versioned_ensembl_gene_id":"ENSG00000238884.1","gene_symbol":"RNU7-85P","gene_name":"RNA, U7 small nuclear 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:34181]","synonyms":"U7.85","biotype":"snRNA","ncbi_id":"100151682","summary":null,"start":79800133,"end":79800195,"strand":-1,"description":"RNA, U7 small nuclear 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:34181]"}, {"versioned_ensembl_gene_id":"ENSG00000284139.1","gene_symbol":"MIR1234","gene_name":"microRNA 1234 [Source:HGNC Symbol;Acc:HGNC:33926]","synonyms":"MIRN1234,hsa-mir-1234","biotype":"miRNA","ncbi_id":"100302196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144400086,"end":144400165,"strand":-1,"description":"microRNA 1234 [Source:HGNC Symbol;Acc:HGNC:33926]"}, {"versioned_ensembl_gene_id":"ENSG00000283622.1","gene_symbol":"MIR4328","gene_name":"microRNA 4328 [Source:HGNC Symbol;Acc:HGNC:38280]","synonyms":"hsa-mir-4328","biotype":"miRNA","ncbi_id":"100422932","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":78901194,"end":78901249,"strand":-1,"description":"microRNA 4328 [Source:HGNC Symbol;Acc:HGNC:38280]"}, {"versioned_ensembl_gene_id":"ENSG00000266168.1","gene_symbol":"MIR3147","gene_name":"microRNA 3147 [Source:HGNC Symbol;Acc:HGNC:38300]","synonyms":"hsa-mir-3147","biotype":"miRNA","ncbi_id":"100422939","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57405025,"end":57405090,"strand":1,"description":"microRNA 3147 [Source:HGNC Symbol;Acc:HGNC:38300]"}, {"versioned_ensembl_gene_id":"ENSG00000207701.1","gene_symbol":"MIR597","gene_name":"microRNA 597 [Source:HGNC Symbol;Acc:HGNC:32853]","synonyms":"MIRN597,hsa-mir-597","biotype":"miRNA","ncbi_id":"693182","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9741672,"end":9741768,"strand":1,"description":"microRNA 597 [Source:HGNC Symbol;Acc:HGNC:32853]"}, {"versioned_ensembl_gene_id":"ENSG00000199023.3","gene_symbol":"MIR339","gene_name":"microRNA 339 [Source:HGNC Symbol;Acc:HGNC:31776]","synonyms":"MIRN339,hsa-mir-339","biotype":"miRNA","ncbi_id":"442907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1022933,"end":1023026,"strand":-1,"description":"microRNA 339 [Source:HGNC Symbol;Acc:HGNC:31776]"}, {"versioned_ensembl_gene_id":"ENSG00000222457.1","gene_symbol":"RNU6-121P","gene_name":"RNA, U6 small nuclear 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:47084]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481215","summary":null,"start":154297650,"end":154297748,"strand":1,"description":"RNA, U6 small nuclear 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:47084]"}, {"versioned_ensembl_gene_id":"ENSG00000264585.1","gene_symbol":"MIR4449","gene_name":"microRNA 4449 [Source:HGNC Symbol;Acc:HGNC:41864]","synonyms":"hsa-mir-4449","biotype":"miRNA","ncbi_id":"100616436","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52712682,"end":52712747,"strand":1,"description":"microRNA 4449 [Source:HGNC Symbol;Acc:HGNC:41864]"}, {"versioned_ensembl_gene_id":"ENSG00000207779.1","gene_symbol":"MIR15B","gene_name":"microRNA 15b [Source:HGNC Symbol;Acc:HGNC:31544]","synonyms":"MIRN15B,hsa-mir-15b","biotype":"miRNA","ncbi_id":"406949","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":160404588,"end":160404685,"strand":1,"description":"microRNA 15b [Source:HGNC Symbol;Acc:HGNC:31544]"}, {"versioned_ensembl_gene_id":"ENSG00000284134.1","gene_symbol":"MIR568","gene_name":"microRNA 568 [Source:HGNC Symbol;Acc:HGNC:32824]","synonyms":"MIRN568,hsa-mir-568","biotype":"miRNA","ncbi_id":"693153","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114316475,"end":114316569,"strand":-1,"description":"microRNA 568 [Source:HGNC Symbol;Acc:HGNC:32824]"}, {"versioned_ensembl_gene_id":"ENSG00000199571.1","gene_symbol":"SNORA22","gene_name":"Small nucleolar RNA SNORA22 [Source:RFAM;Acc:RF00414]","synonyms":"SNORA22A,ACA22","biotype":"snoRNA","ncbi_id":"677807","summary":null,"start":39819750,"end":39819883,"strand":-1,"description":"Small nucleolar RNA SNORA22 [Source:RFAM;Acc:RF00414]"}, {"versioned_ensembl_gene_id":"ENSG00000211590.1","gene_symbol":"MIR802","gene_name":"microRNA 802 [Source:HGNC Symbol;Acc:HGNC:33140]","synonyms":"MIRN802,hsa-mir-802","biotype":"miRNA","ncbi_id":"768219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35720715,"end":35720808,"strand":1,"description":"microRNA 802 [Source:HGNC Symbol;Acc:HGNC:33140]"}, {"versioned_ensembl_gene_id":"ENSG00000274323.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264323,"end":54264425,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207168.1","gene_symbol":"SNORA15","gene_name":"small nucleolar RNA, H/ACA box 15 [Source:HGNC Symbol;Acc:HGNC:32604]","synonyms":"SNORA15A,ACA15","biotype":"snoRNA","ncbi_id":"677803","summary":null,"start":56060470,"end":56060602,"strand":1,"description":"small nucleolar RNA, H/ACA box 15 [Source:HGNC Symbol;Acc:HGNC:32604]"}, {"versioned_ensembl_gene_id":"ENSG00000284079.1","gene_symbol":"MIR4775","gene_name":"microRNA 4775 [Source:HGNC Symbol;Acc:HGNC:41885]","synonyms":"hsa-mir-4775","biotype":"miRNA","ncbi_id":"100616361","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207754807,"end":207754881,"strand":1,"description":"microRNA 4775 [Source:HGNC Symbol;Acc:HGNC:41885]"}, {"versioned_ensembl_gene_id":"ENSG00000275587.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45538099,"end":45538379,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276229.1","gene_symbol":"Six3os1_3","gene_name":"Six3os1 conserved region 3 [Source:RFAM;Acc:RF02248]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44935294,"end":44935368,"strand":1,"description":"Six3os1 conserved region 3 [Source:RFAM;Acc:RF02248]"}, {"versioned_ensembl_gene_id":"ENSG00000251751.1","gene_symbol":"RN7SKP46","gene_name":"RNA, 7SK small nuclear pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45770]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480847","summary":null,"start":157930492,"end":157930725,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45770]"}, {"versioned_ensembl_gene_id":"ENSG00000201558.1","gene_symbol":"RNVU1-6","gene_name":"RNA, variant U1 small nuclear 6 [Source:HGNC Symbol;Acc:HGNC:48314]","synonyms":"vU1.6,RNU1-99","biotype":"snRNA","ncbi_id":"101954276","summary":null,"start":146052081,"end":146052244,"strand":-1,"description":"RNA, variant U1 small nuclear 6 [Source:HGNC Symbol;Acc:HGNC:48314]"}, {"versioned_ensembl_gene_id":"ENSG00000199715.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18273165,"end":18273266,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273788.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":72726122,"end":72726337,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000223040.1","gene_symbol":"RN7SKP144","gene_name":"RNA, 7SK small nuclear pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:45868]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479159","summary":null,"start":2088933,"end":2089211,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 144 [Source:HGNC Symbol;Acc:HGNC:45868]"}, {"versioned_ensembl_gene_id":"ENSG00000242999.3","gene_symbol":"RN7SL239P","gene_name":"RNA, 7SL, cytoplasmic 239, pseudogene [Source:HGNC Symbol;Acc:HGNC:46255]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479309","summary":null,"start":74845910,"end":74846209,"strand":1,"description":"RNA, 7SL, cytoplasmic 239, pseudogene [Source:HGNC Symbol;Acc:HGNC:46255]"}, {"versioned_ensembl_gene_id":"ENSG00000209582.1","gene_symbol":"SNORA48","gene_name":"small nucleolar RNA, H/ACA box 48 [Source:HGNC Symbol;Acc:HGNC:32641]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":7574713,"end":7574847,"strand":1,"description":"small nucleolar RNA, H/ACA box 48 [Source:HGNC Symbol;Acc:HGNC:32641]"}, {"versioned_ensembl_gene_id":"ENSG00000252268.1","gene_symbol":"RNA5SP417","gene_name":"RNA, 5S ribosomal pseudogene 417 [Source:HGNC Symbol;Acc:HGNC:43317]","synonyms":"RN5S417","biotype":"rRNA","ncbi_id":"100873668","summary":null,"start":35751828,"end":35751935,"strand":1,"description":"RNA, 5S ribosomal pseudogene 417 [Source:HGNC Symbol;Acc:HGNC:43317]"}, {"versioned_ensembl_gene_id":"ENSG00000244372.3","gene_symbol":"RN7SL423P","gene_name":"RNA, 7SL, cytoplasmic 423, pseudogene [Source:HGNC Symbol;Acc:HGNC:46439]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479378","summary":null,"start":160877547,"end":160877850,"strand":1,"description":"RNA, 7SL, cytoplasmic 423, pseudogene [Source:HGNC Symbol;Acc:HGNC:46439]"}, {"versioned_ensembl_gene_id":"ENSG00000284284.1","gene_symbol":"MIR4712","gene_name":"microRNA 4712 [Source:HGNC Symbol;Acc:HGNC:41732]","synonyms":"hsa-mir-4712","biotype":"miRNA","ncbi_id":"100616396","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50360329,"end":50360410,"strand":1,"description":"microRNA 4712 [Source:HGNC Symbol;Acc:HGNC:41732]"}, {"versioned_ensembl_gene_id":"ENSG00000207714.3","gene_symbol":"MIR584","gene_name":"microRNA 584 [Source:HGNC Symbol;Acc:HGNC:32840]","synonyms":"MIRN584,hsa-mir-584","biotype":"miRNA","ncbi_id":"693169","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149062313,"end":149062409,"strand":-1,"description":"microRNA 584 [Source:HGNC Symbol;Acc:HGNC:32840]"}, {"versioned_ensembl_gene_id":"ENSG00000274693.1","gene_symbol":"HTT-AS1_2","gene_name":"HTT antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02135]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3069977,"end":3070151,"strand":1,"description":"HTT antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02135]"}, {"versioned_ensembl_gene_id":"ENSG00000264915.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31702742,"end":31702855,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221760.1","gene_symbol":"MIR548J","gene_name":"microRNA 548j [Source:HGNC Symbol;Acc:HGNC:35276]","synonyms":"MIRN548J,hsa-mir-548j","biotype":"miRNA","ncbi_id":"100313914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26555212,"end":26555323,"strand":-1,"description":"microRNA 548j [Source:HGNC Symbol;Acc:HGNC:35276]"}, {"versioned_ensembl_gene_id":"ENSG00000264591.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31523278,"end":31523355,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000284329.1","gene_symbol":"MIR9-3","gene_name":"microRNA 9-3 [Source:HGNC Symbol;Acc:HGNC:31646]","synonyms":"MIRN9-3,hsa-mir-9-3","biotype":"miRNA","ncbi_id":"407051","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89368017,"end":89368106,"strand":1,"description":"microRNA 9-3 [Source:HGNC Symbol;Acc:HGNC:31646]"}, {"versioned_ensembl_gene_id":"ENSG00000278517.1","gene_symbol":"MIR6865","gene_name":"microRNA 6865 [Source:HGNC Symbol;Acc:HGNC:50182]","synonyms":"hsa-mir-6865","biotype":"miRNA","ncbi_id":"102465522","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4970086,"end":4970150,"strand":-1,"description":"microRNA 6865 [Source:HGNC Symbol;Acc:HGNC:50182]"}, {"versioned_ensembl_gene_id":"ENSG00000199460.2","gene_symbol":"RNU6-1216P","gene_name":"RNA, U6 small nuclear 1216, pseudogene [Source:HGNC Symbol;Acc:HGNC:48179]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480098","summary":null,"start":69182877,"end":69182983,"strand":1,"description":"RNA, U6 small nuclear 1216, pseudogene [Source:HGNC Symbol;Acc:HGNC:48179]"}, {"versioned_ensembl_gene_id":"ENSG00000206922.1","gene_symbol":"RNU6-80P","gene_name":"RNA, U6 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:42570]","synonyms":"RNU6-80","biotype":"snRNA","ncbi_id":"106478990","summary":null,"start":72706017,"end":72706123,"strand":-1,"description":"RNA, U6 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:42570]"}, {"versioned_ensembl_gene_id":"ENSG00000199805.1","gene_symbol":"RNU1-134P","gene_name":"RNA, U1 small nuclear 134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48476]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480194","summary":null,"start":63908955,"end":63909119,"strand":1,"description":"RNA, U1 small nuclear 134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48476]"}, {"versioned_ensembl_gene_id":"ENSG00000252839.1","gene_symbol":"RNU6-419P","gene_name":"RNA, U6 small nuclear 419, pseudogene [Source:HGNC Symbol;Acc:HGNC:47382]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479751","summary":null,"start":73246818,"end":73246880,"strand":-1,"description":"RNA, U6 small nuclear 419, pseudogene [Source:HGNC Symbol;Acc:HGNC:47382]"}, {"versioned_ensembl_gene_id":"ENSG00000207248.1","gene_symbol":"RNU6-1005P","gene_name":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481497","summary":null,"start":21642054,"end":21642160,"strand":1,"description":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]"}, {"versioned_ensembl_gene_id":"ENSG00000251908.1","gene_symbol":"RNU6-491P","gene_name":"RNA, U6 small nuclear 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:47454]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479784","summary":null,"start":14250232,"end":14250341,"strand":-1,"description":"RNA, U6 small nuclear 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:47454]"}, {"versioned_ensembl_gene_id":"ENSG00000238597.1","gene_symbol":"SNORD4B","gene_name":"small nucleolar RNA, C/D box 4B [Source:HGNC Symbol;Acc:HGNC:10098]","synonyms":"Z17B,RNU101B","biotype":"snoRNA","ncbi_id":"26772","summary":null,"start":28723682,"end":28723753,"strand":1,"description":"small nucleolar RNA, C/D box 4B [Source:HGNC Symbol;Acc:HGNC:10098]"}, {"versioned_ensembl_gene_id":"ENSG00000265878.2","gene_symbol":"MIR3914-1","gene_name":"microRNA 3914-1 [Source:HGNC Symbol;Acc:HGNC:38993]","synonyms":"hsa-mir-3914-1","biotype":"miRNA","ncbi_id":"100500836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71307672,"end":71307770,"strand":-1,"description":"microRNA 3914-1 [Source:HGNC Symbol;Acc:HGNC:38993]"}, {"versioned_ensembl_gene_id":"ENSG00000148700.14","gene_symbol":"ADD3","gene_name":"adducin 3 [Source:HGNC Symbol;Acc:HGNC:245]","synonyms":"ADDL","biotype":"protein_coding","ncbi_id":"120","summary":"Adducins are heteromeric proteins composed of different subunits referred to as adducin alpha, beta and gamma. The three subunits are encoded by distinct genes and belong to a family of membrane skeletal proteins involved in the assembly of spectrin-actin network in erythrocytes and at sites of cell-cell contact in epithelial tissues. While adducins alpha and gamma are ubiquitously expressed, the expression of adducin beta is restricted to brain and hematopoietic tissues. Adducin, originally purified from human erythrocytes, was found to be a heterodimer of adducins alpha and beta. Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension. Heterodimers consisting of alpha and gamma subunits have also been described. Structurally, each subunit is comprised of two distinct domains. The amino-terminal region is protease resistant and globular in shape, while the carboxy-terminal region is protease sensitive. The latter contains multiple phosphorylation sites for protein kinase C, the binding site for calmodulin, and is required for association with spectrin and actin. Alternatively spliced adducin gamma transcripts encoding different isoforms have been described. The functions of the different isoforms are not known. [provided by RefSeq, Jul 2008]","start":109996368,"end":110135565,"strand":1,"description":"adducin 3 [Source:HGNC Symbol;Acc:HGNC:245]"}, {"versioned_ensembl_gene_id":"ENSG00000267634.1","gene_symbol":"RPL7L1P5","gene_name":"ribosomal protein L7 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390800","summary":null,"start":44365014,"end":44365751,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39487]"}, {"versioned_ensembl_gene_id":"ENSG00000229312.2","gene_symbol":"AL353693.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69472466,"end":69494513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126453.9","gene_symbol":"BCL2L12","gene_name":"BCL2 like 12 [Source:HGNC Symbol;Acc:HGNC:13787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83596","summary":"This gene encodes a member of a family of proteins containing a Bcl-2 homology domain 2 (BH2). The encoded protein is an anti-apoptotic factor that acts as an inhibitor of caspases 3 and 7 in the cytoplasm. In the nucleus, it binds to the p53 tumor suppressor protein, preventing its association with target genes. Overexpression of this gene has been detected in a number of different cancers. There is a pseudogene for this gene on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":49665142,"end":49673916,"strand":1,"description":"BCL2 like 12 [Source:HGNC Symbol;Acc:HGNC:13787]"}, {"versioned_ensembl_gene_id":"ENSG00000280758.1","gene_symbol":"AL356481.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128630328,"end":128631685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108309.13","gene_symbol":"RUNDC3A","gene_name":"RUN domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16984]","synonyms":"RPIP8,RAP2IP","biotype":"protein_coding","ncbi_id":"10900","summary":null,"start":44308413,"end":44318671,"strand":1,"description":"RUN domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16984]"}, {"versioned_ensembl_gene_id":"ENSG00000119333.11","gene_symbol":"WDR34","gene_name":"WD repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:28296]","synonyms":"MGC20486,FAP133,DIC5,bA216B9.3","biotype":"protein_coding","ncbi_id":"89891","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014]","start":128633661,"end":128656787,"strand":-1,"description":"WD repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:28296]"}, {"versioned_ensembl_gene_id":"ENSG00000254462.1","gene_symbol":"TMX2-CTNND1","gene_name":"TMX2-CTNND1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528016","summary":"This locus represents naturally occurring read-through transcription between the neighboring TMX2 (thioredoxin-related transmembrane protein 2) and CTNND1 (catenin, cadherin-associated protein, delta 1) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":57712605,"end":57791586,"strand":1,"description":"TMX2-CTNND1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41992]"}, {"versioned_ensembl_gene_id":"ENSG00000216906.2","gene_symbol":"AL355312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149904243,"end":149906418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239317.1","gene_symbol":"AC091959.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146138771,"end":146139008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126773.12","gene_symbol":"PCNX4","gene_name":"pecanex homolog 4 [Source:HGNC Symbol;Acc:HGNC:20349]","synonyms":"PCNXL4,C14orf135","biotype":"protein_coding","ncbi_id":"64430","summary":null,"start":60091911,"end":60169133,"strand":1,"description":"pecanex homolog 4 [Source:HGNC Symbol;Acc:HGNC:20349]"}, {"versioned_ensembl_gene_id":"ENSG00000224907.1","gene_symbol":"RPL21P91","gene_name":"ribosomal protein L21 pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:36450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271424","summary":null,"start":109807651,"end":109808129,"strand":1,"description":"ribosomal protein L21 pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:36450]"}, {"versioned_ensembl_gene_id":"ENSG00000185813.10","gene_symbol":"PCYT2","gene_name":"phosphate cytidylyltransferase 2, ethanolamine [Source:HGNC Symbol;Acc:HGNC:8756]","synonyms":"ET","biotype":"protein_coding","ncbi_id":"5833","summary":"This gene encodes an enzyme that catalyzes the formation of CDP-ethanolamine from CTP and phosphoethanolamine in the Kennedy pathway of phospholipid synthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":81900965,"end":81911464,"strand":-1,"description":"phosphate cytidylyltransferase 2, ethanolamine [Source:HGNC Symbol;Acc:HGNC:8756]"}, {"versioned_ensembl_gene_id":"ENSG00000249149.2","gene_symbol":"AC099522.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":73382384,"end":73410509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157637.12","gene_symbol":"SLC38A10","gene_name":"solute carrier family 38 member 10 [Source:HGNC Symbol;Acc:HGNC:28237]","synonyms":"PP1744,MGC15523","biotype":"protein_coding","ncbi_id":"124565","summary":null,"start":81245000,"end":81295547,"strand":-1,"description":"solute carrier family 38 member 10 [Source:HGNC Symbol;Acc:HGNC:28237]"}, {"versioned_ensembl_gene_id":"ENSG00000167302.10","gene_symbol":"TEPSIN","gene_name":"TEPSIN, adaptor related protein complex 4 accessory protein [Source:HGNC Symbol;Acc:HGNC:26458]","synonyms":"FLJ31528,ENTHD2,C17orf56","biotype":"protein_coding","ncbi_id":"146705","summary":null,"start":81228277,"end":81239091,"strand":-1,"description":"TEPSIN, adaptor related protein complex 4 accessory protein [Source:HGNC Symbol;Acc:HGNC:26458]"}, {"versioned_ensembl_gene_id":"ENSG00000251599.1","gene_symbol":"AC116345.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73132008,"end":73150592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270236.1","gene_symbol":"AL162730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69107926,"end":69108217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141577.13","gene_symbol":"CEP131","gene_name":"centrosomal protein 131 [Source:HGNC Symbol;Acc:HGNC:29511]","synonyms":"KIAA1118,AZI1,AZ1","biotype":"protein_coding","ncbi_id":"22994","summary":null,"start":81189593,"end":81222999,"strand":-1,"description":"centrosomal protein 131 [Source:HGNC Symbol;Acc:HGNC:29511]"}, {"versioned_ensembl_gene_id":"ENSG00000176681.14","gene_symbol":"LRRC37A","gene_name":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]","synonyms":"KIAA0563,KIAA0563","biotype":"protein_coding","ncbi_id":"9884","summary":null,"start":46292733,"end":46337794,"strand":1,"description":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]"}, {"versioned_ensembl_gene_id":"ENSG00000113073.14","gene_symbol":"SLC4A9","gene_name":"solute carrier family 4 member 9 [Source:HGNC Symbol;Acc:HGNC:11035]","synonyms":"AE4","biotype":"protein_coding","ncbi_id":"83697","summary":"The protein encoded by this gene is a membrane protein involved in anion exchange. Expression of this gene is mostly limited to the kidney. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":140360202,"end":140375143,"strand":1,"description":"solute carrier family 4 member 9 [Source:HGNC Symbol;Acc:HGNC:11035]"}, {"versioned_ensembl_gene_id":"ENSG00000236504.2","gene_symbol":"AC087499.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20647287,"end":20681799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235785.1","gene_symbol":"AL109767.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99262948,"end":99264735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262539.1","gene_symbol":"AC005829.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46259551,"end":46260606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261575.2","gene_symbol":"AC005829.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46267037,"end":46268694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125319.14","gene_symbol":"C17orf53","gene_name":"chromosome 17 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:28460]","synonyms":"MGC3130","biotype":"protein_coding","ncbi_id":"78995","summary":null,"start":44141906,"end":44162476,"strand":1,"description":"chromosome 17 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:28460]"}, {"versioned_ensembl_gene_id":"ENSG00000198393.7","gene_symbol":"ZNF26","gene_name":"zinc finger protein 26 [Source:HGNC Symbol;Acc:HGNC:13053]","synonyms":"KOX20,FLJ20755","biotype":"protein_coding","ncbi_id":"7574","summary":null,"start":132986365,"end":133032952,"strand":1,"description":"zinc finger protein 26 [Source:HGNC Symbol;Acc:HGNC:13053]"}, {"versioned_ensembl_gene_id":"ENSG00000236714.1","gene_symbol":"LINC01844","gene_name":"long intergenic non-protein coding RNA 1844 [Source:HGNC Symbol;Acc:HGNC:52660]","synonyms":"LOC101926975","biotype":"lincRNA","ncbi_id":"101926975","summary":null,"start":142745600,"end":142760998,"strand":1,"description":"long intergenic non-protein coding RNA 1844 [Source:HGNC Symbol;Acc:HGNC:52660]"}, {"versioned_ensembl_gene_id":"ENSG00000261757.1","gene_symbol":"AC005592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142703782,"end":142705421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259775.1","gene_symbol":"AL138976.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103331674,"end":103332367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257900.2","gene_symbol":"AL162632.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45377268,"end":45389286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258608.1","gene_symbol":"DNAJC19P9","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644589","summary":null,"start":45290036,"end":45290386,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45072]"}, {"versioned_ensembl_gene_id":"ENSG00000263278.2","gene_symbol":"AC233701.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79598032,"end":79603921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146005.3","gene_symbol":"PSD2","gene_name":"pleckstrin and Sec7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19092]","synonyms":"EFA6C,DKFZp761B0514","biotype":"protein_coding","ncbi_id":"84249","summary":null,"start":139795821,"end":139844466,"strand":1,"description":"pleckstrin and Sec7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19092]"}, {"versioned_ensembl_gene_id":"ENSG00000148082.9","gene_symbol":"SHC3","gene_name":"SHC adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:18181]","synonyms":"SHCC,NSHC,N-Shc","biotype":"protein_coding","ncbi_id":"53358","summary":null,"start":89005771,"end":89178767,"strand":-1,"description":"SHC adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:18181]"}, {"versioned_ensembl_gene_id":"ENSG00000249131.1","gene_symbol":"PSD2-AS1","gene_name":"PSD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52765]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929696","summary":null,"start":139741349,"end":139746223,"strand":-1,"description":"PSD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52765]"}, {"versioned_ensembl_gene_id":"ENSG00000248729.1","gene_symbol":"MTCO1P30","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52095]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075170","summary":null,"start":5395378,"end":5395957,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52095]"}, {"versioned_ensembl_gene_id":"ENSG00000228658.1","gene_symbol":"AL772202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88971638,"end":88976298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197617.7","gene_symbol":"VN1R5","gene_name":"vomeronasal 1 receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19870]","synonyms":"V1RL5","biotype":"polymorphic_pseudogene","ncbi_id":"317705","summary":null,"start":247255972,"end":247257210,"strand":1,"description":"vomeronasal 1 receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19870]"}, {"versioned_ensembl_gene_id":"ENSG00000150782.11","gene_symbol":"IL18","gene_name":"interleukin 18 [Source:HGNC Symbol;Acc:HGNC:5986]","synonyms":"IL1F4,IL-1g,IL-18,IGIF","biotype":"protein_coding","ncbi_id":"3606","summary":"The protein encoded by this gene is a proinflammatory cytokine of the IL-1 family that is constitutively found as a precursor within the cytoplasm of a variety of cells including macrophages and keratinocytes. The inactive IL-18 precursor is processed to its active form by caspase-1, and is capable of stimulating interferon gamma production, and of regulating both T helper (Th) 1 and Th2 responses. This cytokine has been implicated in the injury of different organs, and in potentially fatal conditions characterized by a cytokine storm. In humans, IL-18 gene is located on chromosome 11. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2020]","start":112143251,"end":112164117,"strand":-1,"description":"interleukin 18 [Source:HGNC Symbol;Acc:HGNC:5986]"}, {"versioned_ensembl_gene_id":"ENSG00000143033.17","gene_symbol":"MTF2","gene_name":"metal response element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29535]","synonyms":"TDRD19A,PCL2,M96","biotype":"protein_coding","ncbi_id":"22823","summary":null,"start":93079235,"end":93139081,"strand":1,"description":"metal response element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29535]"}, {"versioned_ensembl_gene_id":"ENSG00000279339.1","gene_symbol":"AC100788.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78897264,"end":78900152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129197.14","gene_symbol":"RPAIN","gene_name":"RPA interacting protein [Source:HGNC Symbol;Acc:HGNC:28641]","synonyms":"RIP,MGC4189,hRIP","biotype":"protein_coding","ncbi_id":"84268","summary":null,"start":5419641,"end":5432876,"strand":1,"description":"RPA interacting protein [Source:HGNC Symbol;Acc:HGNC:28641]"}, {"versioned_ensembl_gene_id":"ENSG00000263220.1","gene_symbol":"AC015727.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5364315,"end":5371626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198752.10","gene_symbol":"CDC42BPB","gene_name":"CDC42 binding protein kinase beta [Source:HGNC Symbol;Acc:HGNC:1738]","synonyms":"MRCKB,KIAA1124","biotype":"protein_coding","ncbi_id":"9578","summary":"This gene encodes a member of the serine/threonine protein kinase family. The encoded protein contains a Cdc42/Rac-binding p21 binding domain resembling that of PAK kinase. The kinase domain of this protein is most closely related to that of myotonic dystrophy kinase-related ROK. Studies of the similar gene in rat suggested that this kinase may act as a downstream effector of Cdc42 in cytoskeletal reorganization. [provided by RefSeq, Jul 2008]","start":102932379,"end":103057462,"strand":-1,"description":"CDC42 binding protein kinase beta [Source:HGNC Symbol;Acc:HGNC:1738]"}, {"versioned_ensembl_gene_id":"ENSG00000150776.17","gene_symbol":"C11orf57","gene_name":"chromosome 11 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25569]","synonyms":"FLJ10726","biotype":"protein_coding","ncbi_id":"55216","summary":null,"start":112074086,"end":112085150,"strand":1,"description":"chromosome 11 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25569]"}, {"versioned_ensembl_gene_id":"ENSG00000230911.1","gene_symbol":"AP000907.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112029858,"end":112030367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242595.1","gene_symbol":"RPL26P26","gene_name":"ribosomal protein L26 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270967","summary":null,"start":58113189,"end":58113622,"strand":-1,"description":"ribosomal protein L26 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35693]"}, {"versioned_ensembl_gene_id":"ENSG00000227438.1","gene_symbol":"AP001471.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46093264,"end":46097530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274297.1","gene_symbol":"AC009269.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70758269,"end":70758856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140471.16","gene_symbol":"LINS1","gene_name":"lines homolog 1 [Source:HGNC Symbol;Acc:HGNC:30922]","synonyms":"WINS1,LINS","biotype":"protein_coding","ncbi_id":"55180","summary":"The Drosophila segment polarity gene lin encodes a protein, lines, which plays important roles in development of the epidermis and hindgut. This gene encodes a protein containing a lines-like domain. This gene is located on chromosome 15 and clustered with the gene encoding ankyrin repeat and SOCS box-containing protein 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2017]","start":100559369,"end":100603230,"strand":-1,"description":"lines homolog 1 [Source:HGNC Symbol;Acc:HGNC:30922]"}, {"versioned_ensembl_gene_id":"ENSG00000029725.16","gene_symbol":"RABEP1","gene_name":"rabaptin, RAB GTPase binding effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17677]","synonyms":"RABPT5,rabaptin-5,RAB5EP,neurocrescin","biotype":"protein_coding","ncbi_id":"9135","summary":null,"start":5282265,"end":5385812,"strand":1,"description":"rabaptin, RAB GTPase binding effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17677]"}, {"versioned_ensembl_gene_id":"ENSG00000259540.1","gene_symbol":"AC027020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100558677,"end":100559798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253886.1","gene_symbol":"AC026688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154493576,"end":154494743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113196.2","gene_symbol":"HAND1","gene_name":"heart and neural crest derivatives expressed 1 [Source:HGNC Symbol;Acc:HGNC:4807]","synonyms":"Thing1,Hxt,eHand,bHLHa27","biotype":"protein_coding","ncbi_id":"9421","summary":"The protein encoded by this gene belongs to the basic helix-loop-helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, it has been suggested that this transcription factor may be required for early trophoblast differentiation. [provided by RefSeq, Jul 2008]","start":154474972,"end":154478264,"strand":-1,"description":"heart and neural crest derivatives expressed 1 [Source:HGNC Symbol;Acc:HGNC:4807]"}, {"versioned_ensembl_gene_id":"ENSG00000279913.1","gene_symbol":"AP001962.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":99844138,"end":99844696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055483.19","gene_symbol":"USP36","gene_name":"ubiquitin specific peptidase 36 [Source:HGNC Symbol;Acc:HGNC:20062]","synonyms":"KIAA1453,FLJ12851","biotype":"protein_coding","ncbi_id":"57602","summary":"This gene encodes a member of the peptidase C19 or ubiquitin-specific protease family of cysteine proteases. Members of this family remove ubiquitin molecules from polyubiquitinated proteins. The encoded protein may deubiquitinate and stabilize the transcription factor c-Myc, also known as MYC, an important oncoprotein known to be upregulated in most human cancers. The encoded protease may also regulate the activation of autophagy. This gene exhibits elevated expression in some breast and lung cancers. [provided by RefSeq, Mar 2016]","start":78787381,"end":78841441,"strand":-1,"description":"ubiquitin specific peptidase 36 [Source:HGNC Symbol;Acc:HGNC:20062]"}, {"versioned_ensembl_gene_id":"ENSG00000100784.10","gene_symbol":"RPS6KA5","gene_name":"ribosomal protein S6 kinase A5 [Source:HGNC Symbol;Acc:HGNC:10434]","synonyms":"RLPK,MSK1","biotype":"protein_coding","ncbi_id":"9252","summary":null,"start":90847862,"end":91060636,"strand":-1,"description":"ribosomal protein S6 kinase A5 [Source:HGNC Symbol;Acc:HGNC:10434]"}, {"versioned_ensembl_gene_id":"ENSG00000266963.1","gene_symbol":"AC005625.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38361795,"end":38362484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081791.8","gene_symbol":"KIAA0141","gene_name":"KIAA0141 [Source:HGNC Symbol;Acc:HGNC:28969]","synonyms":"DELE","biotype":"protein_coding","ncbi_id":"9812","summary":null,"start":141923808,"end":141942047,"strand":1,"description":"KIAA0141 [Source:HGNC Symbol;Acc:HGNC:28969]"}, {"versioned_ensembl_gene_id":"ENSG00000130560.8","gene_symbol":"UBAC1","gene_name":"UBA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30221]","synonyms":"UBADC1,KPC2,GBDR1","biotype":"protein_coding","ncbi_id":"10422","summary":null,"start":135932969,"end":135961380,"strand":-1,"description":"UBA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30221]"}, {"versioned_ensembl_gene_id":"ENSG00000236703.1","gene_symbol":"MYB-AS1","gene_name":"MYB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37457]","synonyms":"NCRNA00209,MYBAS,MYB-AS,RP1-32B1.3","biotype":"antisense_RNA","ncbi_id":"100873904","summary":null,"start":135195083,"end":135195995,"strand":-1,"description":"MYB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37457]"}, {"versioned_ensembl_gene_id":"ENSG00000238058.1","gene_symbol":"AL355574.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135907812,"end":135913513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179058.6","gene_symbol":"C9orf50","gene_name":"chromosome 9 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:23677]","synonyms":"FLJ35803","biotype":"protein_coding","ncbi_id":"375759","summary":null,"start":129612225,"end":129620776,"strand":-1,"description":"chromosome 9 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:23677]"}, {"versioned_ensembl_gene_id":"ENSG00000254590.1","gene_symbol":"AP003396.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119402792,"end":119404088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267463.1","gene_symbol":"UBE2V2P2","gene_name":"ubiquitin conjugating enzyme E2 V2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44887]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"104548970","summary":null,"start":78066258,"end":78066761,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44887]"}, {"versioned_ensembl_gene_id":"ENSG00000279600.1","gene_symbol":"AC015804.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78008421,"end":78008855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258884.1","gene_symbol":"LINC02321","gene_name":"long intergenic non-protein coding RNA 2321 [Source:HGNC Symbol;Acc:HGNC:53240]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370623","summary":null,"start":90822365,"end":90828128,"strand":-1,"description":"long intergenic non-protein coding RNA 2321 [Source:HGNC Symbol;Acc:HGNC:53240]"}, {"versioned_ensembl_gene_id":"ENSG00000255415.1","gene_symbol":"AP000867.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71629045,"end":71629421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226164.2","gene_symbol":"FGFR3P6","gene_name":"fibroblast growth factor receptor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420881","summary":null,"start":247119669,"end":247120278,"strand":1,"description":"fibroblast growth factor receptor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37951]"}, {"versioned_ensembl_gene_id":"ENSG00000250602.5","gene_symbol":"AC093535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126433505,"end":126490371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037749.11","gene_symbol":"MFAP3","gene_name":"microfibril associated protein 3 [Source:HGNC Symbol;Acc:HGNC:7034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4238","summary":null,"start":154038906,"end":154220478,"strand":1,"description":"microfibril associated protein 3 [Source:HGNC Symbol;Acc:HGNC:7034]"}, {"versioned_ensembl_gene_id":"ENSG00000134480.13","gene_symbol":"CCNH","gene_name":"cyclin H [Source:HGNC Symbol;Acc:HGNC:1594]","synonyms":"p37,p34,CycH","biotype":"protein_coding","ncbi_id":"902","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK7 kinase and ring finger protein MAT1. The kinase complex is able to phosphorylate CDK2 and CDC2 kinases, thus functions as a CDK-activating kinase (CAK). This cyclin and its kinase partner are components of TFIIH, as well as RNA polymerase II protein complexes. They participate in two different transcriptional regulation processes, suggesting an important link between basal transcription control and the cell cycle machinery. A pseudogene of this gene is found on chromosome 4. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Nov 2010]","start":87391494,"end":87413019,"strand":-1,"description":"cyclin H [Source:HGNC Symbol;Acc:HGNC:1594]"}, {"versioned_ensembl_gene_id":"ENSG00000110274.15","gene_symbol":"CEP164","gene_name":"centrosomal protein 164 [Source:HGNC Symbol;Acc:HGNC:29182]","synonyms":"NPHP15,KIAA1052","biotype":"protein_coding","ncbi_id":"22897","summary":"This gene encodes a centrosomal protein involved in microtubule organization, DNA damage response, and chromosome segregation. The encoded protein is required for assembly of primary cilia and localizes to mature centrioles. Defects in this gene are a cause of nephronophthisis-related ciliopathies. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":117314557,"end":117413268,"strand":1,"description":"centrosomal protein 164 [Source:HGNC Symbol;Acc:HGNC:29182]"}, {"versioned_ensembl_gene_id":"ENSG00000255301.1","gene_symbol":"AP002893.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57476493,"end":57477534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186907.7","gene_symbol":"RTN4RL2","gene_name":"reticulon 4 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:23053]","synonyms":"NGRH1,NgR2","biotype":"protein_coding","ncbi_id":"349667","summary":null,"start":57460549,"end":57477534,"strand":1,"description":"reticulon 4 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:23053]"}, {"versioned_ensembl_gene_id":"ENSG00000189068.9","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040825,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000142408.4","gene_symbol":"CACNG8","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:13628]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59283","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type II TARP and a calcium channel gamma subunit. The mRNA for this gene is believed to initiate translation from a non-AUG (CUG) start codon. [provided by RefSeq, Dec 2010]","start":53963040,"end":53990215,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 8 [Source:HGNC Symbol;Acc:HGNC:13628]"}, {"versioned_ensembl_gene_id":"ENSG00000245385.2","gene_symbol":"AP003396.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119336249,"end":119337309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231759.7","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21P,CYP21A,P450c21A","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":31987818,"end":31990633,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000198648.10","gene_symbol":"STK39","gene_name":"serine/threonine kinase 39 [Source:HGNC Symbol;Acc:HGNC:17717]","synonyms":"DCHT,SPAK","biotype":"protein_coding","ncbi_id":"27347","summary":"This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress. [provided by RefSeq, Jul 2008]","start":167954020,"end":168248141,"strand":-1,"description":"serine/threonine kinase 39 [Source:HGNC Symbol;Acc:HGNC:17717]"}, {"versioned_ensembl_gene_id":"ENSG00000228095.3","gene_symbol":"AL354692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84604111,"end":84604425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248352.1","gene_symbol":"TNXA","gene_name":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]","synonyms":"XA,TNX,HXBL,D6S103E","biotype":"unprocessed_pseudogene","ncbi_id":"7146","summary":null,"start":31990796,"end":31994654,"strand":-1,"description":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]"}, {"versioned_ensembl_gene_id":"ENSG00000173456.4","gene_symbol":"RNF26","gene_name":"ring finger protein 26 [Source:HGNC Symbol;Acc:HGNC:14646]","synonyms":"MGC2642","biotype":"protein_coding","ncbi_id":"79102","summary":"The protein encoded by this intronless gene contains a C3HC5 type of RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. The expression of this gene was found to be upregulated in cancer cell lines derived from different types of cancer. [provided by RefSeq, Jul 2008]","start":119334527,"end":119337313,"strand":1,"description":"ring finger protein 26 [Source:HGNC Symbol;Acc:HGNC:14646]"}, {"versioned_ensembl_gene_id":"ENSG00000149212.11","gene_symbol":"SESN3","gene_name":"sestrin 3 [Source:HGNC Symbol;Acc:HGNC:23060]","synonyms":"SEST3,MGC29667","biotype":"protein_coding","ncbi_id":"143686","summary":"This gene encodes a member of the sestrin family of stress-induced proteins. The encoded protein reduces the levels of intracellular reactive oxygen species induced by activated Ras downstream of RAC-alpha serine/threonine-protein kinase (Akt) and FoxO transcription factor. The protein is required for normal regulation of blood glucose, insulin resistance and plays a role in lipid storage in obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":95165513,"end":95232541,"strand":-1,"description":"sestrin 3 [Source:HGNC Symbol;Acc:HGNC:23060]"}, {"versioned_ensembl_gene_id":"ENSG00000251183.1","gene_symbol":"LINC01861","gene_name":"long intergenic non-protein coding RNA 1861 [Source:HGNC Symbol;Acc:HGNC:52680]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378238","summary":null,"start":153887428,"end":153898987,"strand":-1,"description":"long intergenic non-protein coding RNA 1861 [Source:HGNC Symbol;Acc:HGNC:52680]"}, {"versioned_ensembl_gene_id":"ENSG00000240198.5","gene_symbol":"ARHGEF3-AS1","gene_name":"ARHGEF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40083]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874200","summary":null,"start":56940040,"end":56960854,"strand":1,"description":"ARHGEF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40083]"}, {"versioned_ensembl_gene_id":"ENSG00000110665.11","gene_symbol":"C11orf21","gene_name":"chromosome 11 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:13231]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29125","summary":null,"start":2295645,"end":2303049,"strand":-1,"description":"chromosome 11 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:13231]"}, {"versioned_ensembl_gene_id":"ENSG00000223649.1","gene_symbol":"AC105275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":211492255,"end":211492917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112531.16","gene_symbol":"QKI","gene_name":"QKI, KH domain containing RNA binding [Source:HGNC Symbol;Acc:HGNC:21100]","synonyms":"QK3","biotype":"protein_coding","ncbi_id":"9444","summary":"The protein encoded by this gene is an RNA-binding protein that regulates pre-mRNA splicing, export of mRNAs from the nucleus, protein translation, and mRNA stability. The encoded protein is involved in myelinization and oligodendrocyte differentiation and may play a role in schizophrenia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":163414000,"end":163578596,"strand":1,"description":"QKI, KH domain containing RNA binding [Source:HGNC Symbol;Acc:HGNC:21100]"}, {"versioned_ensembl_gene_id":"ENSG00000244411.3","gene_symbol":"KRTAP5-7","gene_name":"keratin associated protein 5-7 [Source:HGNC Symbol;Acc:HGNC:23602]","synonyms":"KRTAP5.7,KRTAP5-3","biotype":"protein_coding","ncbi_id":"440050","summary":null,"start":71527267,"end":71528674,"strand":1,"description":"keratin associated protein 5-7 [Source:HGNC Symbol;Acc:HGNC:23602]"}, {"versioned_ensembl_gene_id":"ENSG00000135723.13","gene_symbol":"FHOD1","gene_name":"formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]","synonyms":"FHOS","biotype":"protein_coding","ncbi_id":"29109","summary":"This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":67229387,"end":67247658,"strand":-1,"description":"formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]"}, {"versioned_ensembl_gene_id":"ENSG00000253203.6","gene_symbol":"GUSBP3","gene_name":"glucuronidase, beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37301]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653188","summary":null,"start":69639459,"end":69679259,"strand":-1,"description":"glucuronidase, beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37301]"}, {"versioned_ensembl_gene_id":"ENSG00000236591.1","gene_symbol":"AL357992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149027700,"end":149032573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229311.1","gene_symbol":"BX088651.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42579414,"end":42586534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250716.1","gene_symbol":"LINC01017","gene_name":"long intergenic non-protein coding RNA 1017 [Source:HGNC Symbol;Acc:HGNC:50641]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467075","summary":null,"start":3496229,"end":3504004,"strand":-1,"description":"long intergenic non-protein coding RNA 1017 [Source:HGNC Symbol;Acc:HGNC:50641]"}, {"versioned_ensembl_gene_id":"ENSG00000258776.1","gene_symbol":"AL161757.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56817570,"end":56893710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236809.2","gene_symbol":"SNX25P1","gene_name":"sorting nexin 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41509]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419028","summary":null,"start":211417025,"end":211417934,"strand":1,"description":"sorting nexin 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41509]"}, {"versioned_ensembl_gene_id":"ENSG00000226864.2","gene_symbol":"ATE1-AS1","gene_name":"ATE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49496]","synonyms":"ENST00000437593","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100130887","summary":null,"start":121928312,"end":121951965,"strand":1,"description":"ATE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49496]"}, {"versioned_ensembl_gene_id":"ENSG00000248648.1","gene_symbol":"AC113410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133003119,"end":133003365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119899.12","gene_symbol":"SLC17A5","gene_name":"solute carrier family 17 member 5 [Source:HGNC Symbol;Acc:HGNC:10933]","synonyms":"SLD,SIASD,SIALIN,SD,NSD,ISSD,AST","biotype":"protein_coding","ncbi_id":"26503","summary":"This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]","start":73593379,"end":73654155,"strand":-1,"description":"solute carrier family 17 member 5 [Source:HGNC Symbol;Acc:HGNC:10933]"}, {"versioned_ensembl_gene_id":"ENSG00000149485.18","gene_symbol":"FADS1","gene_name":"fatty acid desaturase 1 [Source:HGNC Symbol;Acc:HGNC:3574]","synonyms":"D5D,TU12,LLCDL1,FADSD5,FADS6","biotype":"protein_coding","ncbi_id":"3992","summary":"The protein encoded by this gene is a member of the fatty acid desaturase (FADS) gene family. Desaturase enzymes regulate unsaturation of fatty acids through the introduction of double bonds between defined carbons of the fatty acyl chain. FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion, both of which are characterized by conserved histidine motifs. This gene is clustered with family members FADS1 and FADS2 at 11q12-q13.1; this cluster is thought to have arisen evolutionarily from gene duplication based on its similar exon/intron organization. [provided by RefSeq, Jul 2008]","start":61799625,"end":61829318,"strand":-1,"description":"fatty acid desaturase 1 [Source:HGNC Symbol;Acc:HGNC:3574]"}, {"versioned_ensembl_gene_id":"ENSG00000228323.2","gene_symbol":"AC008440.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53854581,"end":53869107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230205.1","gene_symbol":"AL359382.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148133809,"end":148137404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248994.1","gene_symbol":"AC126768.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1933863,"end":1959176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132704.15","gene_symbol":"FCRL2","gene_name":"Fc receptor like 2 [Source:HGNC Symbol;Acc:HGNC:14875]","synonyms":"SPAP1,IRTA4,FCRH2,CD307b","biotype":"protein_coding","ncbi_id":"79368","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains one immunoreceptor-tyrosine activation motif and two immunoreceptor-tyrosine inhibitory motifs. This protein may be a prognostic marker for chronic lymphocytic leukemia. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Apr 2009]","start":157745733,"end":157777132,"strand":-1,"description":"Fc receptor like 2 [Source:HGNC Symbol;Acc:HGNC:14875]"}, {"versioned_ensembl_gene_id":"ENSG00000258803.1","gene_symbol":"AL355103.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56514331,"end":56551309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119715.14","gene_symbol":"ESRRB","gene_name":"estrogen related receptor beta [Source:HGNC Symbol;Acc:HGNC:3473]","synonyms":"NR3B2,ESRL2,ERRbeta,ERRb,ERR2,DFNB35","biotype":"protein_coding","ncbi_id":"2103","summary":"This gene encodes a protein with similarity to the estrogen receptor. Its function is unknown; however, a similar protein in mouse plays an essential role in placental development. [provided by RefSeq, Jul 2008]","start":76310614,"end":76501841,"strand":1,"description":"estrogen related receptor beta [Source:HGNC Symbol;Acc:HGNC:3473]"}, {"versioned_ensembl_gene_id":"ENSG00000259124.1","gene_symbol":"AC008050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76495363,"end":76726712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275734.1","gene_symbol":"AC010538.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89684642,"end":89685304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074855.10","gene_symbol":"ANO8","gene_name":"anoctamin 8 [Source:HGNC Symbol;Acc:HGNC:29329]","synonyms":"TMEM16H,KIAA1623","biotype":"protein_coding","ncbi_id":"57719","summary":null,"start":17323223,"end":17334829,"strand":-1,"description":"anoctamin 8 [Source:HGNC Symbol;Acc:HGNC:29329]"}, {"versioned_ensembl_gene_id":"ENSG00000254171.1","gene_symbol":"AC114321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166128498,"end":166155439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264388.1","gene_symbol":"AC090312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71588537,"end":71588884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220494.4","gene_symbol":"YAP1P1","gene_name":"Yes associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442266","summary":null,"start":147406889,"end":147408281,"strand":1,"description":"Yes associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38016]"}, {"versioned_ensembl_gene_id":"ENSG00000248195.1","gene_symbol":"AC016550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86335024,"end":86335808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090971.4","gene_symbol":"NAT14","gene_name":"N-acetyltransferase 14 (putative) [Source:HGNC Symbol;Acc:HGNC:28918]","synonyms":"KLP1","biotype":"protein_coding","ncbi_id":"57106","summary":null,"start":55485004,"end":55487568,"strand":1,"description":"N-acetyltransferase 14 (putative) [Source:HGNC Symbol;Acc:HGNC:28918]"}, {"versioned_ensembl_gene_id":"ENSG00000109118.13","gene_symbol":"PHF12","gene_name":"PHD finger protein 12 [Source:HGNC Symbol;Acc:HGNC:20816]","synonyms":"PF1,KIAA1523","biotype":"protein_coding","ncbi_id":"57649","summary":null,"start":28905250,"end":28951771,"strand":-1,"description":"PHD finger protein 12 [Source:HGNC Symbol;Acc:HGNC:20816]"}, {"versioned_ensembl_gene_id":"ENSG00000258516.1","gene_symbol":"AL133167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95855548,"end":95866464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153820.12","gene_symbol":"SPHKAP","gene_name":"SPHK1 interactor, AKAP domain containing [Source:HGNC Symbol;Acc:HGNC:30619]","synonyms":"SKIP","biotype":"protein_coding","ncbi_id":"80309","summary":null,"start":227979950,"end":228181645,"strand":-1,"description":"SPHK1 interactor, AKAP domain containing [Source:HGNC Symbol;Acc:HGNC:30619]"}, {"versioned_ensembl_gene_id":"ENSG00000241888.2","gene_symbol":"RPSAP37","gene_name":"ribosomal protein SA pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35844]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270915","summary":null,"start":125966777,"end":125968085,"strand":-1,"description":"ribosomal protein SA pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35844]"}, {"versioned_ensembl_gene_id":"ENSG00000248752.1","gene_symbol":"AC010235.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126076800,"end":126279801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176761.7","gene_symbol":"ZNF285B","gene_name":"zinc finger protein 285B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33262]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"147711","summary":null,"start":44467641,"end":44473227,"strand":1,"description":"zinc finger protein 285B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33262]"}, {"versioned_ensembl_gene_id":"ENSG00000183474.15","gene_symbol":"GTF2H2C","gene_name":"GTF2H2 family member C [Source:HGNC Symbol;Acc:HGNC:31394]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728340","summary":null,"start":69560208,"end":69594723,"strand":1,"description":"GTF2H2 family member C [Source:HGNC Symbol;Acc:HGNC:31394]"}, {"versioned_ensembl_gene_id":"ENSG00000173660.11","gene_symbol":"UQCRH","gene_name":"ubiquinol-cytochrome c reductase hinge protein [Source:HGNC Symbol;Acc:HGNC:12590]","synonyms":"UQCR8,QCR6","biotype":"protein_coding","ncbi_id":"7388","summary":null,"start":46303631,"end":46316776,"strand":1,"description":"ubiquinol-cytochrome c reductase hinge protein [Source:HGNC Symbol;Acc:HGNC:12590]"}, {"versioned_ensembl_gene_id":"ENSG00000167113.10","gene_symbol":"COQ4","gene_name":"coenzyme Q4 [Source:HGNC Symbol;Acc:HGNC:19693]","synonyms":"CGI-92","biotype":"protein_coding","ncbi_id":"51117","summary":"This gene encodes a component of the coenzyme Q biosynthesis pathway. Coenzyme Q, an essential component of the electron transport chain, shuttles electrons between complexes I or II to complex III of the mitochondrial transport chain. This protein appears to play a structural role in stabilizing a complex that contains most of the coenzyme Q biosynthesis enzymes. Mutations in this gene are associated with mitochondrial disorders linked to coenzyme Q deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":128322536,"end":128334072,"strand":1,"description":"coenzyme Q4 [Source:HGNC Symbol;Acc:HGNC:19693]"}, {"versioned_ensembl_gene_id":"ENSG00000162039.14","gene_symbol":"MEIOB","gene_name":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]","synonyms":"MGC35212,C16orf73","biotype":"protein_coding","ncbi_id":"254528","summary":null,"start":1833983,"end":1884294,"strand":-1,"description":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]"}, {"versioned_ensembl_gene_id":"ENSG00000197948.10","gene_symbol":"FCHSD1","gene_name":"FCH and double SH3 domains 1 [Source:HGNC Symbol;Acc:HGNC:25463]","synonyms":"FLJ00007","biotype":"protein_coding","ncbi_id":"89848","summary":null,"start":141639302,"end":141651419,"strand":-1,"description":"FCH and double SH3 domains 1 [Source:HGNC Symbol;Acc:HGNC:25463]"}, {"versioned_ensembl_gene_id":"ENSG00000167112.9","gene_symbol":"TRUB2","gene_name":"TruB pseudouridine synthase family member 2 [Source:HGNC Symbol;Acc:HGNC:17170]","synonyms":"CLONE24922","biotype":"protein_coding","ncbi_id":"26995","summary":"Pseudouridine is an abundant component of rRNAs and tRNAs and is enzymatically generated by isomerization of uridine by pseudouridine synthase (Zucchini et al., 2003 [PubMed 12736709]).[supplied by OMIM, Mar 2008]","start":128305161,"end":128322742,"strand":-1,"description":"TruB pseudouridine synthase family member 2 [Source:HGNC Symbol;Acc:HGNC:17170]"}, {"versioned_ensembl_gene_id":"ENSG00000270876.1","gene_symbol":"ZNF30-AS1","gene_name":"ZNF30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51179]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723513","summary":null,"start":34923299,"end":34926812,"strand":-1,"description":"ZNF30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51179]"}, {"versioned_ensembl_gene_id":"ENSG00000245680.9","gene_symbol":"ZNF585B","gene_name":"zinc finger protein 585B [Source:HGNC Symbol;Acc:HGNC:30948]","synonyms":"SZFP41,FLJ14928","biotype":"protein_coding","ncbi_id":"92285","summary":null,"start":37181579,"end":37218153,"strand":-1,"description":"zinc finger protein 585B [Source:HGNC Symbol;Acc:HGNC:30948]"}, {"versioned_ensembl_gene_id":"ENSG00000232366.1","gene_symbol":"VDAC1P9","gene_name":"voltage dependent anion channel 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391106","summary":null,"start":157724180,"end":157725020,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37484]"}, {"versioned_ensembl_gene_id":"ENSG00000280367.1","gene_symbol":"AP002364.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90223153,"end":90226538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244564.1","gene_symbol":"AC096888.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64445231,"end":64454832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168658.18","gene_symbol":"VWA3B","gene_name":"von Willebrand factor A domain containing 3B [Source:HGNC Symbol;Acc:HGNC:28385]","synonyms":"DKFZp686F2227,MGC26733","biotype":"protein_coding","ncbi_id":"200403","summary":"This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]","start":98087116,"end":98313299,"strand":1,"description":"von Willebrand factor A domain containing 3B [Source:HGNC Symbol;Acc:HGNC:28385]"}, {"versioned_ensembl_gene_id":"ENSG00000225698.3","gene_symbol":"IGHV3-72","gene_name":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28410","summary":null,"start":106790691,"end":106791233,"strand":-1,"description":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]"}, {"versioned_ensembl_gene_id":"ENSG00000171421.12","gene_symbol":"MRPL36","gene_name":"mitochondrial ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:14490]","synonyms":"RPMJ,PRPL36,MRP-L36,L36mt,BRIP1","biotype":"protein_coding","ncbi_id":"64979","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 2p. [provided by RefSeq, Jul 2008]","start":1798386,"end":1801366,"strand":-1,"description":"mitochondrial ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:14490]"}, {"versioned_ensembl_gene_id":"ENSG00000188176.11","gene_symbol":"SMTNL2","gene_name":"smoothelin like 2 [Source:HGNC Symbol;Acc:HGNC:24764]","synonyms":"FLJ42461","biotype":"protein_coding","ncbi_id":"342527","summary":null,"start":4583999,"end":4608319,"strand":1,"description":"smoothelin like 2 [Source:HGNC Symbol;Acc:HGNC:24764]"}, {"versioned_ensembl_gene_id":"ENSG00000263733.1","gene_symbol":"AC091691.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71225704,"end":71226721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273361.1","gene_symbol":"AC021016.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":218398743,"end":218399219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105287.12","gene_symbol":"PRKD2","gene_name":"protein kinase D2 [Source:HGNC Symbol;Acc:HGNC:17293]","synonyms":"PKD2,HSPC187,DKFZP586E0820","biotype":"protein_coding","ncbi_id":"25865","summary":"The protein encoded by this gene belongs to the protein kinase D (PKD) family of serine/threonine protein kinases. This kinase can be activated by phorbol esters as well as by gastrin via the cholecystokinin B receptor (CCKBR) in gastric cancer cells. It can bind to diacylglycerol (DAG) in the trans-Golgi network (TGN) and may regulate basolateral membrane protein exit from TGN. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":46674275,"end":46717127,"strand":-1,"description":"protein kinase D2 [Source:HGNC Symbol;Acc:HGNC:17293]"}, {"versioned_ensembl_gene_id":"ENSG00000116748.21","gene_symbol":"AMPD1","gene_name":"adenosine monophosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:468]","synonyms":"MADA,MAD","biotype":"protein_coding","ncbi_id":"270","summary":"Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]","start":114673090,"end":114695618,"strand":-1,"description":"adenosine monophosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:468]"}, {"versioned_ensembl_gene_id":"ENSG00000163597.14","gene_symbol":"SNHG16","gene_name":"small nucleolar RNA host gene 16 [Source:HGNC Symbol;Acc:HGNC:44352]","synonyms":"ncRAN,Nbla12061,Nbla10727","biotype":"processed_transcript","ncbi_id":"100507246","summary":null,"start":76557766,"end":76565348,"strand":1,"description":"small nucleolar RNA host gene 16 [Source:HGNC Symbol;Acc:HGNC:44352]"}, {"versioned_ensembl_gene_id":"ENSG00000153896.17","gene_symbol":"ZNF599","gene_name":"zinc finger protein 599 [Source:HGNC Symbol;Acc:HGNC:26408]","synonyms":"FLJ30663","biotype":"protein_coding","ncbi_id":"148103","summary":null,"start":34758076,"end":34773229,"strand":-1,"description":"zinc finger protein 599 [Source:HGNC Symbol;Acc:HGNC:26408]"}, {"versioned_ensembl_gene_id":"ENSG00000276329.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54861173,"end":54875478,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000160613.12","gene_symbol":"PCSK7","gene_name":"proprotein convertase subtilisin/kexin type 7 [Source:HGNC Symbol;Acc:HGNC:8748]","synonyms":"PC8,PC7,LPC,SPC7","biotype":"protein_coding","ncbi_id":"9159","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It can process proalbumin and is thought to be responsible for the activation of HIV envelope glycoproteins gp160 and gp140. This gene has been implicated in the transcriptional regulation of housekeeping genes and plays a role in the regulation of iron metabolism. A t(11;14)(q23;q32) chromosome translocation associated with B-cell lymphoma occurs between this gene and its inverted counterpart. [provided by RefSeq, Feb 2014]","start":117204337,"end":117232525,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 7 [Source:HGNC Symbol;Acc:HGNC:8748]"}, {"versioned_ensembl_gene_id":"ENSG00000228486.10","gene_symbol":"LINC01125","gene_name":"long intergenic non-protein coding RNA 1125 [Source:HGNC Symbol;Acc:HGNC:49272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728537","summary":null,"start":97664217,"end":97703064,"strand":1,"description":"long intergenic non-protein coding RNA 1125 [Source:HGNC Symbol;Acc:HGNC:49272]"}, {"versioned_ensembl_gene_id":"ENSG00000267142.1","gene_symbol":"AC092296.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36421536,"end":36422534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227857.2","gene_symbol":"AL358075.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46134531,"end":46139081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262303.1","gene_symbol":"AL021878.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42124281,"end":42127775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277345.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877376,"end":54892982,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000276676.5","gene_symbol":"GU182345.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54782658,"end":54797195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240298.3","gene_symbol":"AC015820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25588475,"end":25588795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255454.1","gene_symbol":"AC100770.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25630720,"end":25631041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196415.9","gene_symbol":"PRTN3","gene_name":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]","synonyms":"PR-3,P29,MBT,C-ANCA,AGP7,ACPA","biotype":"protein_coding","ncbi_id":"5657","summary":null,"start":840960,"end":848175,"strand":1,"description":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]"}, {"versioned_ensembl_gene_id":"ENSG00000197665.7","gene_symbol":"AC007952.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19155727,"end":19159111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261070.1","gene_symbol":"AP003071.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69147228,"end":69171564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259084.6","gene_symbol":"AL133467.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":95663256,"end":95692630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120029.12","gene_symbol":"C10orf76","gene_name":"chromosome 10 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25788]","synonyms":"FLJ13114","biotype":"protein_coding","ncbi_id":"79591","summary":null,"start":101845599,"end":102056193,"strand":-1,"description":"chromosome 10 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25788]"}, {"versioned_ensembl_gene_id":"ENSG00000144736.13","gene_symbol":"SHQ1","gene_name":"SHQ1, H/ACA ribonucleoprotein assembly factor [Source:HGNC Symbol;Acc:HGNC:25543]","synonyms":"Shq1p,FLJ10539","biotype":"protein_coding","ncbi_id":"55164","summary":"SHQ1 assists in the assembly of H/ACA-box ribonucleoproteins that function in the processing of ribosomal RNAs, modification of spliceosomal small nuclear RNAs, and stabilization of telomerase (see MIM 602322) (Grozdanov et al., 2009 [PubMed 19383767]).[supplied by OMIM, Dec 2010]","start":72749277,"end":72861914,"strand":-1,"description":"SHQ1, H/ACA ribonucleoprotein assembly factor [Source:HGNC Symbol;Acc:HGNC:25543]"}, {"versioned_ensembl_gene_id":"ENSG00000260249.2","gene_symbol":"AC007608.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50666211,"end":50671639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108106.13","gene_symbol":"UBE2S","gene_name":"ubiquitin conjugating enzyme E2 S [Source:HGNC Symbol;Acc:HGNC:17895]","synonyms":"E2-EPF","biotype":"protein_coding","ncbi_id":"27338","summary":"This gene encodes a member of the ubiquitin-conjugating enzyme family. The encoded protein is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme-dependent manner, a characteristic property of ubiquitin carrier proteins. [provided by RefSeq, Jul 2008]","start":55399745,"end":55407777,"strand":-1,"description":"ubiquitin conjugating enzyme E2 S [Source:HGNC Symbol;Acc:HGNC:17895]"}, {"versioned_ensembl_gene_id":"ENSG00000162852.13","gene_symbol":"CNST","gene_name":"consortin, connexin sorting protein [Source:HGNC Symbol;Acc:HGNC:26486]","synonyms":"PPP1R64,FLJ32001,C1orf71","biotype":"protein_coding","ncbi_id":"163882","summary":"Targeting of numerous transmembrane proteins to the cell surface is thought to depend on their recognition by cargo receptors that interact with the adaptor machinery for anterograde traffic at the distal end of the Golgi complex. Consortin (CNST) is an integral membrane protein that acts as a binding partner of connexins, the building blocks of gap junctions, and acts as a trans-Golgi network (TGN) receptor involved in connexin targeting to the plasma membrane and recycling from the cell surface (del Castillo et al., 2010 [PubMed 19864490]).[supplied by OMIM, Jun 2010]","start":246566444,"end":246668584,"strand":1,"description":"consortin, connexin sorting protein [Source:HGNC Symbol;Acc:HGNC:26486]"}, {"versioned_ensembl_gene_id":"ENSG00000170819.4","gene_symbol":"BFSP2","gene_name":"beaded filament structural protein 2 [Source:HGNC Symbol;Acc:HGNC:1041]","synonyms":"phakinin,LIFL-L,CP49,CP47","biotype":"protein_coding","ncbi_id":"8419","summary":"More than 99% of the vertebrate ocular lens is comprised of terminally differentiated lens fiber cells. Two lens-specific intermediate filament-like proteins, the protein product of this gene (phakinin), and filensin, are expressed only after fiber cell differentiation has begun. Both proteins are found in a structurally unique cytoskeletal element that is referred to as the beaded filament (BF). Mutations in this gene have been associated with juvenile-onset, progressive cataracts and Dowling-Meara epidermolysis bullosa simplex. [provided by RefSeq, Jun 2009]","start":133399995,"end":133475222,"strand":1,"description":"beaded filament structural protein 2 [Source:HGNC Symbol;Acc:HGNC:1041]"}, {"versioned_ensembl_gene_id":"ENSG00000144868.13","gene_symbol":"TMEM108","gene_name":"transmembrane protein 108 [Source:HGNC Symbol;Acc:HGNC:28451]","synonyms":"MGC3040,CT124","biotype":"protein_coding","ncbi_id":"66000","summary":null,"start":133038391,"end":133397792,"strand":1,"description":"transmembrane protein 108 [Source:HGNC Symbol;Acc:HGNC:28451]"}, {"versioned_ensembl_gene_id":"ENSG00000176438.12","gene_symbol":"SYNE3","gene_name":"spectrin repeat containing nuclear envelope family member 3 [Source:HGNC Symbol;Acc:HGNC:19861]","synonyms":"LINC00341,FLJ25605,C14orf49,C14orf139,NET53,Nesprin-3,Nesp3,NCRNA00341","biotype":"protein_coding","ncbi_id":"161176","summary":null,"start":95407266,"end":95475836,"strand":-1,"description":"spectrin repeat containing nuclear envelope family member 3 [Source:HGNC Symbol;Acc:HGNC:19861]"}, {"versioned_ensembl_gene_id":"ENSG00000276412.1","gene_symbol":"AL591926.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41651935,"end":41652172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072571.19","gene_symbol":"HMMR","gene_name":"hyaluronan mediated motility receptor [Source:HGNC Symbol;Acc:HGNC:5012]","synonyms":"RHAMM,CD168","biotype":"protein_coding","ncbi_id":"3161","summary":"The protein encoded by this gene is involved in cell motility. It is expressed in breast tissue and together with other proteins, it forms a complex with BRCA1 and BRCA2, thus is potentially associated with higher risk of breast cancer. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Dec 2008]","start":163460203,"end":163491945,"strand":1,"description":"hyaluronan mediated motility receptor [Source:HGNC Symbol;Acc:HGNC:5012]"}, {"versioned_ensembl_gene_id":"ENSG00000170788.13","gene_symbol":"DYDC1","gene_name":"DPY30 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23460]","synonyms":"DPY30D1,bA36D19.5","biotype":"protein_coding","ncbi_id":"143241","summary":"This gene encodes a member of a family of proteins that contains a DPY30 domain. The encoded protein is involved in acrosome formation during spermatid development. This gene locus overlaps with a closely related gene on the opposite strand. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":80336105,"end":80356755,"strand":-1,"description":"DPY30 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23460]"}, {"versioned_ensembl_gene_id":"ENSG00000253132.1","gene_symbol":"IGHV3-62","gene_name":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28416","summary":null,"start":106643142,"end":106643585,"strand":-1,"description":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]"}, {"versioned_ensembl_gene_id":"ENSG00000255903.2","gene_symbol":"RPL12P46","gene_name":"ribosomal protein L12 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:51938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075251","summary":null,"start":115578049,"end":115578243,"strand":1,"description":"ribosomal protein L12 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:51938]"}, {"versioned_ensembl_gene_id":"ENSG00000259650.1","gene_symbol":"AC068397.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73335260,"end":73342387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229334.1","gene_symbol":"AC046143.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":194632923,"end":194645401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261066.1","gene_symbol":"AC074052.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8526549,"end":8532013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206512.6","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587374,"end":29588957,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000151332.18","gene_symbol":"MBIP","gene_name":"MAP3K12 binding inhibitory protein 1 [Source:HGNC Symbol;Acc:HGNC:20427]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51562","summary":null,"start":36298558,"end":36320676,"strand":-1,"description":"MAP3K12 binding inhibitory protein 1 [Source:HGNC Symbol;Acc:HGNC:20427]"}, {"versioned_ensembl_gene_id":"ENSG00000281692.1","gene_symbol":"PACRG-AS1","gene_name":"PACRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27772]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285796","summary":null,"start":163309985,"end":163324530,"strand":-1,"description":"PACRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27772]"}, {"versioned_ensembl_gene_id":"ENSG00000188611.14","gene_symbol":"ASAH2","gene_name":"N-acylsphingosine amidohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:18860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56624","summary":"Ceramidases (EC 3.5.1.23), such as ASAH2, catalyze hydrolysis of the N-acyl linkage of ceramide, a second messenger in a variety of cellular events, to produce sphingosine. Sphingosine exerts both mitogenic and apoptosis-inducing activities, and its phosphorylated form functions as an intra- and intercellular second messenger (see MIM 603730) (Mitsutake et al., 2001 [PubMed 11328816]).[supplied by OMIM, Mar 2008]","start":50182778,"end":50248610,"strand":-1,"description":"N-acylsphingosine amidohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:18860]"}, {"versioned_ensembl_gene_id":"ENSG00000225683.5","gene_symbol":"PACRG-AS3","gene_name":"PACRG antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:52053]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729658","summary":null,"start":163165414,"end":163192002,"strand":-1,"description":"PACRG antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:52053]"}, {"versioned_ensembl_gene_id":"ENSG00000240974.1","gene_symbol":"RPS27AP10","gene_name":"ribosomal protein S27a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36570]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271377","summary":null,"start":141588935,"end":141589142,"strand":1,"description":"ribosomal protein S27a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36570]"}, {"versioned_ensembl_gene_id":"ENSG00000133247.13","gene_symbol":"KMT5C","gene_name":"lysine methyltransferase 5C [Source:HGNC Symbol;Acc:HGNC:28405]","synonyms":"SUV420H2,MGC2705","biotype":"protein_coding","ncbi_id":"84787","summary":"SUV420H2 and the related enzyme SUV420H1 (MIM 610881) function as histone methyltransferases that specifically trimethylate nucleosomal histone H4 (see MIM 602822) on lysine-20 (K20) (Schotta et al., 2004 [PubMed 15145825]).[supplied by OMIM, Dec 2009]","start":55339853,"end":55348120,"strand":1,"description":"lysine methyltransferase 5C [Source:HGNC Symbol;Acc:HGNC:28405]"}, {"versioned_ensembl_gene_id":"ENSG00000132128.16","gene_symbol":"LRRC41","gene_name":"leucine rich repeat containing 41 [Source:HGNC Symbol;Acc:HGNC:16917]","synonyms":"MUF1","biotype":"protein_coding","ncbi_id":"10489","summary":null,"start":46261196,"end":46303608,"strand":-1,"description":"leucine rich repeat containing 41 [Source:HGNC Symbol;Acc:HGNC:16917]"}, {"versioned_ensembl_gene_id":"ENSG00000224542.7","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30102946,"end":30105603,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000166426.7","gene_symbol":"CRABP1","gene_name":"cellular retinoic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2338]","synonyms":"RBP5,CRABPI,CRABP-I,CRABP","biotype":"protein_coding","ncbi_id":"1381","summary":"This gene encodes a specific binding protein for a vitamin A family member and is thought to play an important role in retinoic acid-mediated differentiation and proliferation processes. It is structurally similar to the cellular retinol-binding proteins, but binds only retinoic acid at specific sites within the nucleus, which may contribute to vitamin A-directed differentiation in epithelial tissue. [provided by RefSeq, Jul 2008]","start":78340324,"end":78348230,"strand":1,"description":"cellular retinoic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2338]"}, {"versioned_ensembl_gene_id":"ENSG00000246422.2","gene_symbol":"AC008781.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141558311,"end":141565263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239736.2","gene_symbol":"CEACAMP3","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]","synonyms":"CGM10,CEACAM24P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1092","summary":null,"start":41599735,"end":41605984,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]"}, {"versioned_ensembl_gene_id":"ENSG00000109339.20","gene_symbol":"MAPK10","gene_name":"mitogen-activated protein kinase 10 [Source:HGNC Symbol;Acc:HGNC:6872]","synonyms":"PRKM10,p54bSAPK,p493F12,JNK3","biotype":"protein_coding","ncbi_id":"5602","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as integration points for multiple biochemical signals, and thus are involved in a wide variety of cellular processes, such as proliferation, differentiation, transcription regulation and development. This kinase is specifically expressed in a subset of neurons in the nervous system, and is activated by threonine and tyrosine phosphorylation. Targeted deletion of this gene in mice suggests that it may have a role in stress-induced neuronal apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]","start":85990007,"end":86594625,"strand":-1,"description":"mitogen-activated protein kinase 10 [Source:HGNC Symbol;Acc:HGNC:6872]"}, {"versioned_ensembl_gene_id":"ENSG00000205363.5","gene_symbol":"C15orf59","gene_name":"chromosome 15 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:33753]","synonyms":"MGC131524,LOC388135,INSYN1","biotype":"protein_coding","ncbi_id":"388135","summary":null,"start":73735431,"end":73752747,"strand":-1,"description":"chromosome 15 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:33753]"}, {"versioned_ensembl_gene_id":"ENSG00000278473.1","gene_symbol":"IGHV3-41","gene_name":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28428","summary":null,"start":106443133,"end":106443583,"strand":-1,"description":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]"}, {"versioned_ensembl_gene_id":"ENSG00000235618.7","gene_symbol":"FAM21EP","gene_name":"family with sequence similarity 21 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:45010]","synonyms":"FLJ31813","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421577","summary":null,"start":50021182,"end":50067803,"strand":-1,"description":"family with sequence similarity 21 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:45010]"}, {"versioned_ensembl_gene_id":"ENSG00000180061.9","gene_symbol":"TMEM150B","gene_name":"transmembrane protein 150B [Source:HGNC Symbol;Acc:HGNC:34415]","synonyms":"TTN2,TMEM224","biotype":"protein_coding","ncbi_id":"284417","summary":"This gene encodes a protein that belongs to the DRAM (damage-regulated autophagy modulator) family of membrane-spanning proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":55312801,"end":55334048,"strand":-1,"description":"transmembrane protein 150B [Source:HGNC Symbol;Acc:HGNC:34415]"}, {"versioned_ensembl_gene_id":"ENSG00000138639.17","gene_symbol":"ARHGAP24","gene_name":"Rho GTPase activating protein 24 [Source:HGNC Symbol;Acc:HGNC:25361]","synonyms":"FLJ33877,FilGAP,DKFZP564B1162","biotype":"protein_coding","ncbi_id":"83478","summary":"This gene encodes a Rho-GTPase activating protein, which is specific for the small GTPase family member Rac. Binding of the encoded protein by filamin A targets it to sites of membrane protrusion, where it antognizes Rac. This results in suppression of lamellae formation and promotion of retraction to regulate cell polarity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":85475114,"end":86002670,"strand":1,"description":"Rho GTPase activating protein 24 [Source:HGNC Symbol;Acc:HGNC:25361]"}, {"versioned_ensembl_gene_id":"ENSG00000138623.9","gene_symbol":"SEMA7A","gene_name":"semaphorin 7A (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:HGNC:10741]","synonyms":"SEMAL,H-Sema-L,CD108","biotype":"protein_coding","ncbi_id":"8482","summary":"This gene encodes a member of the semaphorin family of proteins. The encoded preproprotein is proteolytically processed to generate the mature glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein. The encoded protein is found on activated lymphocytes and erythrocytes and may be involved in immunomodulatory and neuronal processes. The encoded protein carries the John Milton Hagen (JMH) blood group antigens. Mutations in this gene may be associated with reduced bone mineral density (BMD). Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":74409289,"end":74434467,"strand":-1,"description":"semaphorin 7A (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:HGNC:10741]"}, {"versioned_ensembl_gene_id":"ENSG00000277362.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803533,"end":54814482,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000261092.1","gene_symbol":"LINC02178","gene_name":"long intergenic non-protein coding RNA 2178 [Source:HGNC Symbol;Acc:HGNC:53040]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371248","summary":null,"start":50390916,"end":50395133,"strand":-1,"description":"long intergenic non-protein coding RNA 2178 [Source:HGNC Symbol;Acc:HGNC:53040]"}, {"versioned_ensembl_gene_id":"ENSG00000230813.1","gene_symbol":"AL356583.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246527030,"end":246528155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255418.5","gene_symbol":"AC090092.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23164900,"end":23203161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237470.3","gene_symbol":"DCLRE1CP1","gene_name":"DNA cross-link repair 1C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44877]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105376432","summary":null,"start":15015370,"end":15021863,"strand":-1,"description":"DNA cross-link repair 1C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44877]"}, {"versioned_ensembl_gene_id":"ENSG00000274912.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754924,"end":54767305,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000253240.1","gene_symbol":"IGHV3-36","gene_name":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28431","summary":null,"start":106392774,"end":106393231,"strand":-1,"description":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]"}, {"versioned_ensembl_gene_id":"ENSG00000204851.6","gene_symbol":"PNMA8B","gene_name":"paraneoplastic Ma antigen family member 8B [Source:HGNC Symbol;Acc:HGNC:29206]","synonyms":"PNMAL2,KIAA1183","biotype":"protein_coding","ncbi_id":"57469","summary":null,"start":46486906,"end":46496498,"strand":-1,"description":"paraneoplastic Ma antigen family member 8B [Source:HGNC Symbol;Acc:HGNC:29206]"}, {"versioned_ensembl_gene_id":"ENSG00000253325.1","gene_symbol":"IGHV7-34-1","gene_name":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28382","summary":null,"start":106377300,"end":106377733,"strand":-1,"description":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]"}, {"versioned_ensembl_gene_id":"ENSG00000270750.1","gene_symbol":"AC080078.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152320544,"end":152321044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254825.1","gene_symbol":"OR9G2P","gene_name":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]","synonyms":"OR9G6","biotype":"unprocessed_pseudogene","ncbi_id":"81160","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56751023,"end":56751902,"strand":-1,"description":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]"}, {"versioned_ensembl_gene_id":"ENSG00000038427.15","gene_symbol":"VCAN","gene_name":"versican [Source:HGNC Symbol;Acc:HGNC:2464]","synonyms":"PG-M,CSPG2","biotype":"protein_coding","ncbi_id":"1462","summary":"This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":83471465,"end":83582303,"strand":1,"description":"versican [Source:HGNC Symbol;Acc:HGNC:2464]"}, {"versioned_ensembl_gene_id":"ENSG00000100462.15","gene_symbol":"PRMT5","gene_name":"protein arginine methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10894]","synonyms":"SKB1Hs,SKB1,HRMT1L5","biotype":"protein_coding","ncbi_id":"10419","summary":"This gene encodes an enzyme that belongs to the methyltransferase family. The encoded protein catalyzes the transfer of methyl groups to the amino acid arginine, in target proteins that include histones, transcriptional elongation factors and the tumor suppressor p53. This gene plays a role in several cellular processes, including transcriptional regulation, and the assembly of small nuclear ribonucleoproteins. A pseudogene of this gene has been defined on chromosome 4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":22920511,"end":22929585,"strand":-1,"description":"protein arginine methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10894]"}, {"versioned_ensembl_gene_id":"ENSG00000248830.1","gene_symbol":"ZNF807","gene_name":"zinc finger protein 807 [Source:HGNC Symbol;Acc:HGNC:33229]","synonyms":"ZNF807P,ZNF181P1","biotype":"unprocessed_pseudogene","ncbi_id":"100129800","summary":null,"start":34542462,"end":34545395,"strand":-1,"description":"zinc finger protein 807 [Source:HGNC Symbol;Acc:HGNC:33229]"}, {"versioned_ensembl_gene_id":"ENSG00000249835.2","gene_symbol":"VCAN-AS1","gene_name":"VCAN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40163]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105379054","summary":null,"start":83531352,"end":83581320,"strand":-1,"description":"VCAN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40163]"}, {"versioned_ensembl_gene_id":"ENSG00000271034.1","gene_symbol":"AC139700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70125070,"end":70126609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114779.19","gene_symbol":"ABHD14B","gene_name":"abhydrolase domain containing 14B [Source:HGNC Symbol;Acc:HGNC:28235]","synonyms":"MGC15429,CIB","biotype":"protein_coding","ncbi_id":"84836","summary":null,"start":51968510,"end":51983409,"strand":-1,"description":"abhydrolase domain containing 14B [Source:HGNC Symbol;Acc:HGNC:28235]"}, {"versioned_ensembl_gene_id":"ENSG00000181325.7","gene_symbol":"OR9G3P","gene_name":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81159","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56740179,"end":56741096,"strand":1,"description":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]"}, {"versioned_ensembl_gene_id":"ENSG00000270437.1","gene_symbol":"AC009501.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63083008,"end":63087322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254953.1","gene_symbol":"AP001803.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56736316,"end":56736462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142279.12","gene_symbol":"WTIP","gene_name":"WT1 interacting protein [Source:HGNC Symbol;Acc:HGNC:20964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126374","summary":null,"start":34481638,"end":34512304,"strand":1,"description":"WT1 interacting protein [Source:HGNC Symbol;Acc:HGNC:20964]"}, {"versioned_ensembl_gene_id":"ENSG00000131748.15","gene_symbol":"STARD3","gene_name":"StAR related lipid transfer domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17579]","synonyms":"MLN64,es64","biotype":"protein_coding","ncbi_id":"10948","summary":"This gene encodes a member of a subfamily of lipid trafficking proteins that are characterized by a C-terminal steroidogenic acute regulatory domain and an N-terminal metastatic lymph node 64 domain. The encoded protein localizes to the membranes of late endosomes and may be involved in exporting cholesterol. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":39637065,"end":39663484,"strand":1,"description":"StAR related lipid transfer domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17579]"}, {"versioned_ensembl_gene_id":"ENSG00000253482.1","gene_symbol":"IGHVII-26-2","gene_name":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]","synonyms":"IGHV(II)-26-2","biotype":"IG_V_pseudogene","ncbi_id":"28373","summary":null,"start":106314651,"end":106314975,"strand":-1,"description":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]"}, {"versioned_ensembl_gene_id":"ENSG00000239415.1","gene_symbol":"AP001469.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46251549,"end":46254133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234746.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"dJ80I19.4,OR6-8,hs6M1-6","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173300,"end":29174571,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000119685.19","gene_symbol":"TTLL5","gene_name":"tubulin tyrosine ligase like 5 [Source:HGNC Symbol;Acc:HGNC:19963]","synonyms":"KIAA0998","biotype":"protein_coding","ncbi_id":"23093","summary":"This gene encodes a member of the tubulin tyrosine ligase like protein family. This protein interacts with two glucocorticoid receptor coactivators, transcriptional intermediary factor 2 and steroid receptor coactivator 1. This protein may function as a coregulator of glucocorticoid receptor mediated gene induction and repression. This protein may also function as an alpha tubulin polyglutamylase.[provided by RefSeq, Feb 2010]","start":75633625,"end":75955078,"strand":1,"description":"tubulin tyrosine ligase like 5 [Source:HGNC Symbol;Acc:HGNC:19963]"}, {"versioned_ensembl_gene_id":"ENSG00000070748.18","gene_symbol":"CHAT","gene_name":"choline O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:1912]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1103","summary":"This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq, May 2010]","start":49609095,"end":49665104,"strand":1,"description":"choline O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:1912]"}, {"versioned_ensembl_gene_id":"ENSG00000241351.3","gene_symbol":"IGKV3-11","gene_name":"immunoglobulin kappa variable 3-11 [Source:HGNC Symbol;Acc:HGNC:5815]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28914","summary":null,"start":89027171,"end":89027731,"strand":-1,"description":"immunoglobulin kappa variable 3-11 [Source:HGNC Symbol;Acc:HGNC:5815]"}, {"versioned_ensembl_gene_id":"ENSG00000276545.1","gene_symbol":"AC005618.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":141439853,"end":141442449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253278.1","gene_symbol":"IGKV2-10","gene_name":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28928","summary":null,"start":89019992,"end":89020686,"strand":-1,"description":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]"}, {"versioned_ensembl_gene_id":"ENSG00000262576.2","gene_symbol":"PCDHGA4","gene_name":"protocadherin gamma subfamily A, 4 [Source:HGNC Symbol;Acc:HGNC:8702]","synonyms":"PCDH-GAMMA-A4","biotype":"protein_coding","ncbi_id":"56111","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141355025,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 4 [Source:HGNC Symbol;Acc:HGNC:8702]"}, {"versioned_ensembl_gene_id":"ENSG00000189348.6","gene_symbol":"FAM90A27P","gene_name":"family with sequence similarity 90 member A27, pseudogene [Source:HGNC Symbol;Acc:HGNC:43617]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646508","summary":null,"start":53281559,"end":53284944,"strand":1,"description":"family with sequence similarity 90 member A27, pseudogene [Source:HGNC Symbol;Acc:HGNC:43617]"}, {"versioned_ensembl_gene_id":"ENSG00000253233.1","gene_symbol":"AP005902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39867436,"end":39867812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271635.1","gene_symbol":"AC017002.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111558413,"end":111559937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230499.1","gene_symbol":"AC108463.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111195963,"end":111206494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227992.1","gene_symbol":"AC108463.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111203964,"end":111206215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284690.1","gene_symbol":"AC079325.2","gene_name":null,"synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":null,"summary":null,"start":74560701,"end":74567343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215812.5","gene_symbol":"ZNF847P","gene_name":"zinc finger protein 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:34384]","synonyms":"gm127","biotype":"unprocessed_pseudogene","ncbi_id":"401983","summary":null,"start":227696892,"end":227706699,"strand":-1,"description":"zinc finger protein 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:34384]"}, {"versioned_ensembl_gene_id":"ENSG00000223570.2","gene_symbol":"AL592045.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226188870,"end":226189221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155090.14","gene_symbol":"KLF10","gene_name":"Kruppel like factor 10 [Source:HGNC Symbol;Acc:HGNC:11810]","synonyms":"TIEG1,TIEG,EGRA","biotype":"protein_coding","ncbi_id":"7071","summary":"This gene encodes a member of a family of proteins that feature C2H2-type zinc finger domains. The encoded protein is a transcriptional repressor that acts as an effector of transforming growth factor beta signaling. Activity of this protein may inhibit the growth of cancers, particularly pancreatic cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":102648779,"end":102655902,"strand":-1,"description":"Kruppel like factor 10 [Source:HGNC Symbol;Acc:HGNC:11810]"}, {"versioned_ensembl_gene_id":"ENSG00000119699.7","gene_symbol":"TGFB3","gene_name":"transforming growth factor beta 3 [Source:HGNC Symbol;Acc:HGNC:11769]","synonyms":"ARVD1,ARVD","biotype":"protein_coding","ncbi_id":"7043","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGF-beta family members. This protein is involved in embryogenesis and cell differentiation, and may play a role in wound healing. Mutations in this gene are a cause of aortic aneurysms and dissections, as well as familial arrhythmogenic right ventricular dysplasia 1. [provided by RefSeq, Aug 2016]","start":75958099,"end":75982991,"strand":-1,"description":"transforming growth factor beta 3 [Source:HGNC Symbol;Acc:HGNC:11769]"}, {"versioned_ensembl_gene_id":"ENSG00000259103.1","gene_symbol":"AF107885.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75814502,"end":75847698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177291.3","gene_symbol":"GJD4","gene_name":"gap junction protein delta 4 [Source:HGNC Symbol;Acc:HGNC:23296]","synonyms":"FLJ90023,CX40.1","biotype":"protein_coding","ncbi_id":"219770","summary":"Connexins, such as GJD4, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]","start":35605410,"end":35608935,"strand":1,"description":"gap junction protein delta 4 [Source:HGNC Symbol;Acc:HGNC:23296]"}, {"versioned_ensembl_gene_id":"ENSG00000253831.1","gene_symbol":"ETV3L","gene_name":"ETS variant 3 like [Source:HGNC Symbol;Acc:HGNC:33834]","synonyms":"FLJ16478","biotype":"protein_coding","ncbi_id":"440695","summary":null,"start":157092044,"end":157099808,"strand":-1,"description":"ETS variant 3 like [Source:HGNC Symbol;Acc:HGNC:33834]"}, {"versioned_ensembl_gene_id":"ENSG00000224520.2","gene_symbol":"KRT8P45","gene_name":"keratin 8 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39879]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"149501","summary":null,"start":157073257,"end":157074703,"strand":1,"description":"keratin 8 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39879]"}, {"versioned_ensembl_gene_id":"ENSG00000242511.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29724363,"end":29724833,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000159882.12","gene_symbol":"ZNF230","gene_name":"zinc finger protein 230 [Source:HGNC Symbol;Acc:HGNC:13024]","synonyms":"FDZF2","biotype":"protein_coding","ncbi_id":"7773","summary":null,"start":44002948,"end":44013926,"strand":1,"description":"zinc finger protein 230 [Source:HGNC Symbol;Acc:HGNC:13024]"}, {"versioned_ensembl_gene_id":"ENSG00000230805.6","gene_symbol":"AL132709.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101073869,"end":101077910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213030.5","gene_symbol":"CGB8","gene_name":"chorionic gonadotropin beta subunit 8 [Source:HGNC Symbol;Acc:HGNC:16453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94115","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 8 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]","start":49047638,"end":49049106,"strand":-1,"description":"chorionic gonadotropin beta subunit 8 [Source:HGNC Symbol;Acc:HGNC:16453]"}, {"versioned_ensembl_gene_id":"ENSG00000277806.1","gene_symbol":"AC006213.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43976815,"end":43977448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186185.13","gene_symbol":"KIF18B","gene_name":"kinesin family member 18B [Source:HGNC Symbol;Acc:HGNC:27102]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146909","summary":null,"start":44924709,"end":44947711,"strand":-1,"description":"kinesin family member 18B [Source:HGNC Symbol;Acc:HGNC:27102]"}, {"versioned_ensembl_gene_id":"ENSG00000019186.9","gene_symbol":"CYP24A1","gene_name":"cytochrome P450 family 24 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2602]","synonyms":"P450-CC24,CYP24,CP24","biotype":"protein_coding","ncbi_id":"1591","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein initiates the degradation of 1,25-dihydroxyvitamin D3, the physiologically active form of vitamin D3, by hydroxylation of the side chain. In regulating the level of vitamin D3, this enzyme plays a role in calcium homeostasis and the vitamin D endocrine system. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54153449,"end":54173973,"strand":-1,"description":"cytochrome P450 family 24 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2602]"}, {"versioned_ensembl_gene_id":"ENSG00000223615.2","gene_symbol":"AL807761.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107115784,"end":107115954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249633.1","gene_symbol":"OR52V1P","gene_name":"olfactory receptor family 52 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15238]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81242","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5527277,"end":5528174,"strand":-1,"description":"olfactory receptor family 52 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15238]"}, {"versioned_ensembl_gene_id":"ENSG00000165533.18","gene_symbol":"TTC8","gene_name":"tetratricopeptide repeat domain 8 [Source:HGNC Symbol;Acc:HGNC:20087]","synonyms":"RP51,BBS8","biotype":"protein_coding","ncbi_id":"123016","summary":"This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":88824153,"end":88881078,"strand":1,"description":"tetratricopeptide repeat domain 8 [Source:HGNC Symbol;Acc:HGNC:20087]"}, {"versioned_ensembl_gene_id":"ENSG00000119660.4","gene_symbol":"DPPA5P4","gene_name":"developmental pluripotency associated 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49665]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646701","summary":null,"start":75292131,"end":75292495,"strand":-1,"description":"developmental pluripotency associated 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49665]"}, {"versioned_ensembl_gene_id":"ENSG00000226645.1","gene_symbol":"AP006216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116773389,"end":116774205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105427.9","gene_symbol":"CNFN","gene_name":"cornifelin [Source:HGNC Symbol;Acc:HGNC:30183]","synonyms":"PLAC8L2","biotype":"protein_coding","ncbi_id":"84518","summary":null,"start":42387019,"end":42390287,"strand":-1,"description":"cornifelin [Source:HGNC Symbol;Acc:HGNC:30183]"}, {"versioned_ensembl_gene_id":"ENSG00000138622.3","gene_symbol":"HCN4","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium channel 4 [Source:HGNC Symbol;Acc:HGNC:16882]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10021","summary":"This gene encodes a member of the hyperpolarization-activated cyclic nucleotide-gated potassium channels. The encoded protein shows slow kinetics of activation and inactivation, and is necessary for the cardiac pacemaking process. This channel may also mediate responses to sour stimuli. Mutations in this gene have been linked to sick sinus syndrome 2, also known as atrial fibrillation with bradyarrhythmia or familial sinus bradycardia. Two pseudogenes have been identified on chromosome 15. [provided by RefSeq, Oct 2008]","start":73319859,"end":73369264,"strand":-1,"description":"hyperpolarization activated cyclic nucleotide gated potassium channel 4 [Source:HGNC Symbol;Acc:HGNC:16882]"}, {"versioned_ensembl_gene_id":"ENSG00000215417.12","gene_symbol":"MIR17HG","gene_name":"miR-17-92a-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:23564]","synonyms":"FLJ14178,C13orf25,NCRNA00048,MIRHG1,MIRH1,miR-17-92,MIHG1,LINC00048","biotype":"processed_transcript","ncbi_id":"407975","summary":"This gene is the host gene for the MIR17-92 cluster, a group of at least six microRNAs (miRNAs) that may be involved in cell survival, proliferation, differentiation, and angiogenesis. Amplification of this gene has been found in several lymphomas and solid tumors. Two non-protein coding transcript variants have been found for this host gene, but only the longest is a polycistronic transcript containing the MIR17-92 cluster. [provided by RefSeq, May 2012]","start":91347820,"end":91354579,"strand":1,"description":"miR-17-92a-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:23564]"}, {"versioned_ensembl_gene_id":"ENSG00000268879.1","gene_symbol":"IGFL1P1","gene_name":"IGF like family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32956]","synonyms":"IGFL-5P","biotype":"unprocessed_pseudogene","ncbi_id":"727703","summary":null,"start":46196238,"end":46197323,"strand":1,"description":"IGF like family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32956]"}, {"versioned_ensembl_gene_id":"ENSG00000221974.11","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFIIH,TFB2,P52","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30897757,"end":30903679,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000250838.1","gene_symbol":"AC091133.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48995266,"end":48997492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251550.1","gene_symbol":"AC091133.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49037122,"end":49037429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224371.5","gene_symbol":"AL391361.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160872888,"end":160918649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226629.1","gene_symbol":"LINC00974","gene_name":"long intergenic non-protein coding RNA 974 [Source:HGNC Symbol;Acc:HGNC:27105]","synonyms":null,"biotype":"lincRNA","ncbi_id":"147093","summary":null,"start":41549606,"end":41554495,"strand":-1,"description":"long intergenic non-protein coding RNA 974 [Source:HGNC Symbol;Acc:HGNC:27105]"}, {"versioned_ensembl_gene_id":"ENSG00000274903.1","gene_symbol":"AL109933.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160773988,"end":160783214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197937.12","gene_symbol":"ZNF347","gene_name":"zinc finger protein 347 [Source:HGNC Symbol;Acc:HGNC:16447]","synonyms":"ZNF1111","biotype":"protein_coding","ncbi_id":"84671","summary":null,"start":53124072,"end":53159075,"strand":-1,"description":"zinc finger protein 347 [Source:HGNC Symbol;Acc:HGNC:16447]"}, {"versioned_ensembl_gene_id":"ENSG00000148143.12","gene_symbol":"ZNF462","gene_name":"zinc finger protein 462 [Source:HGNC Symbol;Acc:HGNC:21684]","synonyms":"DKFZP762N2316,Zfp462,KIAA1803","biotype":"protein_coding","ncbi_id":"58499","summary":"The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":106863097,"end":107013634,"strand":1,"description":"zinc finger protein 462 [Source:HGNC Symbol;Acc:HGNC:21684]"}, {"versioned_ensembl_gene_id":"ENSG00000230782.1","gene_symbol":"AL807761.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106974833,"end":107102988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227983.1","gene_symbol":"BRK1P2","gene_name":"BRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874492","summary":null,"start":91023732,"end":91023954,"strand":-1,"description":"BRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42021]"}, {"versioned_ensembl_gene_id":"ENSG00000274898.1","gene_symbol":"AC001226.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77027944,"end":77028482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214593.3","gene_symbol":"AL354710.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125263845,"end":125264090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125875.13","gene_symbol":"TBC1D20","gene_name":"TBC1 domain family member 20 [Source:HGNC Symbol;Acc:HGNC:16133]","synonyms":"dJ852M4.2,C20orf140","biotype":"protein_coding","ncbi_id":"128637","summary":"This gene encodes a protein that belongs to a family of GTPase activator proteins of Rab-like small GTPases. The encoded protein and its cognate GTPase, Rab1, bind the nonstructural protein 5A (NS5A) of the hepatitis C virus (HCV) to mediate viral replication. Depletion of this protein inhibits replication of the virus and HCV infection. Mutations in this gene are associated with Warburg micro syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":435480,"end":462553,"strand":-1,"description":"TBC1 domain family member 20 [Source:HGNC Symbol;Acc:HGNC:16133]"}, {"versioned_ensembl_gene_id":"ENSG00000234202.2","gene_symbol":"AC104332.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92749175,"end":92749330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231674.1","gene_symbol":"LINC00410","gene_name":"long intergenic non-protein coding RNA 410 [Source:HGNC Symbol;Acc:HGNC:42742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"144776","summary":null,"start":90890954,"end":90926597,"strand":-1,"description":"long intergenic non-protein coding RNA 410 [Source:HGNC Symbol;Acc:HGNC:42742]"}, {"versioned_ensembl_gene_id":"ENSG00000235317.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCG4P10,HCGIV.9,HCGIV-10","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29789145,"end":29790142,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000149599.15","gene_symbol":"DUSP15","gene_name":"dual specificity phosphatase 15 [Source:HGNC Symbol;Acc:HGNC:16236]","synonyms":"VHY,FLJ20645,C20orf57,bA243J16.6,bA243J16.5","biotype":"protein_coding","ncbi_id":"128853","summary":"The protein encoded by this gene has both protein-tyrosine phophatase activity and serine/threonine-specific phosphatase activity, and therefore is known as a dual specificity phosphatase. This protein may function in the differentiation of oligodendrocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":31847637,"end":31870747,"strand":-1,"description":"dual specificity phosphatase 15 [Source:HGNC Symbol;Acc:HGNC:16236]"}, {"versioned_ensembl_gene_id":"ENSG00000167740.9","gene_symbol":"CYB5D2","gene_name":"cytochrome b5 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28471]","synonyms":"MGC32124","biotype":"protein_coding","ncbi_id":"124936","summary":null,"start":4143168,"end":4187310,"strand":1,"description":"cytochrome b5 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28471]"}, {"versioned_ensembl_gene_id":"ENSG00000139330.5","gene_symbol":"KERA","gene_name":"keratocan [Source:HGNC Symbol;Acc:HGNC:6309]","synonyms":"SLRR2B,CNA2","biotype":"protein_coding","ncbi_id":"11081","summary":"The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by RefSeq, May 2010]","start":91050491,"end":91057983,"strand":-1,"description":"keratocan [Source:HGNC Symbol;Acc:HGNC:6309]"}, {"versioned_ensembl_gene_id":"ENSG00000185722.16","gene_symbol":"ANKFY1","gene_name":"ankyrin repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20763]","synonyms":"BTBD23,ANKHZN,ZFYVE14,RANK-5,KIAA1255","biotype":"protein_coding","ncbi_id":"51479","summary":"This gene encodes a cytoplasmic protein that contains a coiled-coil structure and a BTB/POZ domain at its N-terminus, ankyrin repeats in the middle portion, and a FYVE-finger motif at its C-terminus. This protein belongs to a subgroup of double zinc finger proteins which may be involved in vesicle or protein transport. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Apr 2012]","start":4163907,"end":4263977,"strand":-1,"description":"ankyrin repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20763]"}, {"versioned_ensembl_gene_id":"ENSG00000240237.1","gene_symbol":"AF305872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133002605,"end":133003075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224419.1","gene_symbol":"KRT18P27","gene_name":"keratin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33396]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390418","summary":null,"start":90230384,"end":90231682,"strand":1,"description":"keratin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33396]"}, {"versioned_ensembl_gene_id":"ENSG00000275549.1","gene_symbol":"STPG3-AS1","gene_name":"STPG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51176]","synonyms":"C9orf173-AS1","biotype":"antisense_RNA","ncbi_id":"100129722","summary":null,"start":137250219,"end":137253497,"strand":-1,"description":"STPG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51176]"}, {"versioned_ensembl_gene_id":"ENSG00000223465.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"B144,LST-1,D6S49E","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31568266,"end":31571053,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000066923.17","gene_symbol":"STAG3","gene_name":"stromal antigen 3 [Source:HGNC Symbol;Acc:HGNC:11356]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10734","summary":"The protein encoded by this gene is expressed in the nucleus and is a subunit of the cohesin complex which regulates the cohesion of sister chromatids during cell division. A mutation in this gene is associated with premature ovarian failure. Alternate splicing results in multiple transcript variants encoding distinct isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Apr 2014]","start":100177563,"end":100221488,"strand":1,"description":"stromal antigen 3 [Source:HGNC Symbol;Acc:HGNC:11356]"}, {"versioned_ensembl_gene_id":"ENSG00000251395.1","gene_symbol":"FTH1P9","gene_name":"ferritin heavy chain 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39089]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478936","summary":null,"start":83426676,"end":83427030,"strand":1,"description":"ferritin heavy chain 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39089]"}, {"versioned_ensembl_gene_id":"ENSG00000237468.2","gene_symbol":"AL359547.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146594516,"end":146598931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213736.2","gene_symbol":"AC026310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24967127,"end":24967504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131738.10","gene_symbol":"KRT33B","gene_name":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]","synonyms":"KRTHA3B,Ha-3II","biotype":"protein_coding","ncbi_id":"3884","summary":"This gene encodes a member of the keratin gene family. This gene is one of multiple type I hair keratin genes that are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. As a type I hair keratin, the encoded protein is an acidic protein which heterodimerizes with type II keratins to form hair and nails. There are two isoforms of this protein, encoded by two separate genes, keratin 33A and keratin 33B. [provided by RefSeq, May 2012]","start":41363494,"end":41369800,"strand":-1,"description":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]"}, {"versioned_ensembl_gene_id":"ENSG00000275828.1","gene_symbol":"AC134879.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11412548,"end":11418716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270242.1","gene_symbol":"ACTR3BP1","gene_name":"ACTR3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643050","summary":null,"start":11395699,"end":11397076,"strand":1,"description":"ACTR3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37724]"}, {"versioned_ensembl_gene_id":"ENSG00000182938.4","gene_symbol":"OTOP3","gene_name":"otopetrin 3 [Source:HGNC Symbol;Acc:HGNC:19658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347741","summary":null,"start":74935719,"end":74949992,"strand":1,"description":"otopetrin 3 [Source:HGNC Symbol;Acc:HGNC:19658]"}, {"versioned_ensembl_gene_id":"ENSG00000039650.11","gene_symbol":"PNKP","gene_name":"polynucleotide kinase 3'-phosphatase [Source:HGNC Symbol;Acc:HGNC:9154]","synonyms":"PNK","biotype":"protein_coding","ncbi_id":"11284","summary":"This locus represents a gene involved in DNA repair. In response to ionizing radiation or oxidative damage, the protein encoded by this locus catalyzes 5' phosphorylation and 3' dephosphorylation of nucleic acids. Mutations at this locus have been associated with microcephaly, seizures, and developmental delay.[provided by RefSeq, Sep 2010]","start":49859882,"end":49878351,"strand":-1,"description":"polynucleotide kinase 3'-phosphatase [Source:HGNC Symbol;Acc:HGNC:9154]"}, {"versioned_ensembl_gene_id":"ENSG00000162947.4","gene_symbol":"LINC01931","gene_name":"long intergenic non-protein coding RNA 1931 [Source:HGNC Symbol;Acc:HGNC:52743]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150596","summary":null,"start":149767506,"end":149859191,"strand":-1,"description":"long intergenic non-protein coding RNA 1931 [Source:HGNC Symbol;Acc:HGNC:52743]"}, {"versioned_ensembl_gene_id":"ENSG00000171793.13","gene_symbol":"CTPS1","gene_name":"CTP synthase 1 [Source:HGNC Symbol;Acc:HGNC:2519]","synonyms":"GATD5,CTPS","biotype":"protein_coding","ncbi_id":"1503","summary":"This gene encodes an enzyme responsible for the catalytic conversion of UTP (uridine triphosphate) to CTP (cytidine triphospate). This reaction is an important step in the biosynthesis of phospholipids and nucleic acids. Activity of this proten is important in the immune system, and loss of function of this gene has been associated with immunodeficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":40979335,"end":41012565,"strand":1,"description":"CTP synthase 1 [Source:HGNC Symbol;Acc:HGNC:2519]"}, {"versioned_ensembl_gene_id":"ENSG00000283101.1","gene_symbol":"BMS1P21","gene_name":"BMS1, ribosome biogenesis factor pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51604]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288974","summary":null,"start":79906605,"end":79907856,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51604]"}, {"versioned_ensembl_gene_id":"ENSG00000133661.15","gene_symbol":"SFTPD","gene_name":"surfactant protein D [Source:HGNC Symbol;Acc:HGNC:10803]","synonyms":"SP-D,SFTP4,COLEC7","biotype":"protein_coding","ncbi_id":"6441","summary":"The protein encoded by this gene is part of the innate immune response, protecting the lungs against inhaled microorganisms and chemicals. The encoded protein may also be involved in surfactant metabolism. [provided by RefSeq, Jul 2015]","start":79937740,"end":79982614,"strand":-1,"description":"surfactant protein D [Source:HGNC Symbol;Acc:HGNC:10803]"}, {"versioned_ensembl_gene_id":"ENSG00000223496.2","gene_symbol":"EXOSC6","gene_name":"exosome component 6 [Source:HGNC Symbol;Acc:HGNC:19055]","synonyms":"p11,Mtr3p,MTR3,hMtr3p,EAP4","biotype":"protein_coding","ncbi_id":"118460","summary":"This gene product constitutes one of the subunits of the multisubunit particle called exosome, which mediates mRNA degradation. The composition of human exosome is similar to its yeast counterpart. This protein is homologous to the yeast Mtr3 protein. Its exact function is not known, however, it has been shown using a cell-free RNA decay system that the exosome is required for rapid degradation of unstable mRNAs containing AU-rich elements (AREs), but not for poly(A) shortening. The exosome does not recognize ARE-containing mRNAs on its own, but requires ARE-binding proteins that could interact with the exosome and recruit it to unstable mRNAs, thereby promoting their rapid degradation. [provided by RefSeq, Jul 2008]","start":70246778,"end":70251930,"strand":-1,"description":"exosome component 6 [Source:HGNC Symbol;Acc:HGNC:19055]"}, {"versioned_ensembl_gene_id":"ENSG00000113296.14","gene_symbol":"THBS4","gene_name":"thrombospondin 4 [Source:HGNC Symbol;Acc:HGNC:11788]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7060","summary":"The protein encoded by this gene belongs to the thrombospondin protein family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentamer and can bind to heparin and calcium. It is involved in local signaling in the developing and adult nervous system, and it contributes to spinal sensitization and neuropathic pain states. This gene is activated during the stromal response to invasive breast cancer. It may also play a role in inflammatory responses in Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":79991311,"end":80083287,"strand":1,"description":"thrombospondin 4 [Source:HGNC Symbol;Acc:HGNC:11788]"}, {"versioned_ensembl_gene_id":"ENSG00000259399.1","gene_symbol":"TGIF2-C20orf24","gene_name":"TGIF2-C20orf24 readthrough [Source:HGNC Symbol;Acc:HGNC:44664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527943","summary":"This locus represents naturally occurring read-through transcription between the neighboring TGIF2 (TGFB-induced factor homeobox 2) and C20orf24 (chromosome 20 open reading frame 24) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010]","start":36574553,"end":36612384,"strand":1,"description":"TGIF2-C20orf24 readthrough [Source:HGNC Symbol;Acc:HGNC:44664]"}, {"versioned_ensembl_gene_id":"ENSG00000249825.5","gene_symbol":"CTD-2201I18.1","gene_name":"uncharacterized LOC101929215 [Source:NCBI gene;Acc:101929215]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929215","summary":null,"start":80052374,"end":80083654,"strand":-1,"description":"uncharacterized LOC101929215 [Source:NCBI gene;Acc:101929215]"}, {"versioned_ensembl_gene_id":"ENSG00000242779.6","gene_symbol":"ZNF702P","gene_name":"zinc finger protein 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:25775]","synonyms":"ZNF702,FLJ12985","biotype":"transcribed_processed_pseudogene","ncbi_id":"79986","summary":null,"start":52968251,"end":53037898,"strand":-1,"description":"zinc finger protein 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:25775]"}, {"versioned_ensembl_gene_id":"ENSG00000253726.1","gene_symbol":"AC013562.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":72732045,"end":72751843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254705.1","gene_symbol":"AP000722.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92400191,"end":92408176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179772.7","gene_symbol":"FOXS1","gene_name":"forkhead box S1 [Source:HGNC Symbol;Acc:HGNC:3735]","synonyms":"FREAC10,FKHL18","biotype":"protein_coding","ncbi_id":"2307","summary":"The forkhead family of transcription factors belongs to the winged helix class of DNA-binding proteins. The protein encoded by this intronless gene contains a forkhead domain and is found predominantly in aorta and kidney. The function of the encoded protein is unknown. [provided by RefSeq, Jul 2008]","start":31844301,"end":31845619,"strand":-1,"description":"forkhead box S1 [Source:HGNC Symbol;Acc:HGNC:3735]"}, {"versioned_ensembl_gene_id":"ENSG00000227963.1","gene_symbol":"AL355488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110286375,"end":110339171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240845.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29724152,"end":29724622,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000233617.1","gene_symbol":"CR753818.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720462,"end":29721452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263923.1","gene_symbol":"AC019131.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98928897,"end":98994994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179546.4","gene_symbol":"HTR1D","gene_name":"5-hydroxytryptamine receptor 1D [Source:HGNC Symbol;Acc:HGNC:5289]","synonyms":"RDC4,HTRL,HT1DA,5-HT1D","biotype":"protein_coding","ncbi_id":"3352","summary":null,"start":23191895,"end":23194729,"strand":-1,"description":"5-hydroxytryptamine receptor 1D [Source:HGNC Symbol;Acc:HGNC:5289]"}, {"versioned_ensembl_gene_id":"ENSG00000118322.12","gene_symbol":"ATP10B","gene_name":"ATPase phospholipid transporting 10B (putative) [Source:HGNC Symbol;Acc:HGNC:13543]","synonyms":"KIAA0715,FLJ21477,ATPVB","biotype":"protein_coding","ncbi_id":"23120","summary":null,"start":160563120,"end":160852214,"strand":-1,"description":"ATPase phospholipid transporting 10B (putative) [Source:HGNC Symbol;Acc:HGNC:13543]"}, {"versioned_ensembl_gene_id":"ENSG00000253796.1","gene_symbol":"AC104248.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108895029,"end":109063417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196119.7","gene_symbol":"OR8A1","gene_name":"olfactory receptor family 8 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8469]","synonyms":"OST025","biotype":"protein_coding","ncbi_id":"390275","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124566660,"end":124582942,"strand":1,"description":"olfactory receptor family 8 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8469]"}, {"versioned_ensembl_gene_id":"ENSG00000170953.3","gene_symbol":"OR8B12","gene_name":"olfactory receptor family 8 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15307]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219858","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124539635,"end":124545333,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15307]"}, {"versioned_ensembl_gene_id":"ENSG00000271503.5","gene_symbol":"CCL5","gene_name":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]","synonyms":"TCP228,SISd,SCYA5,RANTES,MGC17164,D17S136E","biotype":"protein_coding","ncbi_id":"6352","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, functions as a chemoattractant for blood monocytes, memory T helper cells and eosinophils. It causes the release of histamine from basophils and activates eosinophils. This cytokine is one of the major HIV-suppressive factors produced by CD8+ cells. It functions as one of the natural ligands for the chemokine receptor chemokine (C-C motif) receptor 5 (CCR5), and it suppresses in vitro replication of the R5 strains of HIV-1, which use CCR5 as a coreceptor. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":35871491,"end":35880793,"strand":-1,"description":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]"}, {"versioned_ensembl_gene_id":"ENSG00000229503.1","gene_symbol":"AC092155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62532583,"end":62533059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069493.14","gene_symbol":"CLEC2D","gene_name":"C-type lectin domain family 2 member D [Source:HGNC Symbol;Acc:HGNC:14351]","synonyms":"LLT1,CLAX,OCIL","biotype":"protein_coding","ncbi_id":"29121","summary":"This gene encodes a member of the natural killer cell receptor C-type lectin family. The encoded protein inhibits osteoclast formation and contains a transmembrane domain near the N-terminus as well as the C-type lectin-like extracellular domain. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Oct 2010]","start":9664969,"end":9699555,"strand":1,"description":"C-type lectin domain family 2 member D [Source:HGNC Symbol;Acc:HGNC:14351]"}, {"versioned_ensembl_gene_id":"ENSG00000240156.1","gene_symbol":"COX6CP6","gene_name":"cytochrome c oxidase subunit 6C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:47037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289131","summary":null,"start":70751123,"end":70751350,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:47037]"}, {"versioned_ensembl_gene_id":"ENSG00000227091.1","gene_symbol":"AL355990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110166186,"end":110172489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235526.1","gene_symbol":"AL355990.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110177643,"end":110178719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268218.1","gene_symbol":"AC137932.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89268104,"end":89273044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270832.1","gene_symbol":"AC092120.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89458870,"end":89459437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129566.12","gene_symbol":"TEP1","gene_name":"telomerase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:11726]","synonyms":"VAULT2,TROVE1,TP1,TLP1,p240","biotype":"protein_coding","ncbi_id":"7011","summary":"This gene product is a component of the ribonucleoprotein complex responsible for telomerase activity which catalyzes the addition of new telomeres on the chromosome ends. The telomerase-associated proteins are conserved from ciliates to humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":20365667,"end":20413429,"strand":-1,"description":"telomerase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:11726]"}, {"versioned_ensembl_gene_id":"ENSG00000259056.1","gene_symbol":"DUXAP1","gene_name":"double homeobox A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32180]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"503630","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":84750769,"end":84751231,"strand":1,"description":"double homeobox A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32180]"}, {"versioned_ensembl_gene_id":"ENSG00000231150.5","gene_symbol":"AL034345.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38923029,"end":38953099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196912.12","gene_symbol":"ANKRD36B","gene_name":"ankyrin repeat domain 36B [Source:HGNC Symbol;Acc:HGNC:29333]","synonyms":"KIAA1641,FLJ21281","biotype":"protein_coding","ncbi_id":"57730","summary":null,"start":97492663,"end":97589965,"strand":-1,"description":"ankyrin repeat domain 36B [Source:HGNC Symbol;Acc:HGNC:29333]"}, {"versioned_ensembl_gene_id":"ENSG00000227825.4","gene_symbol":"SLC9A7P1","gene_name":"solute carrier family 9 member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32679]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"121456","summary":null,"start":98453835,"end":98457145,"strand":-1,"description":"solute carrier family 9 member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32679]"}, {"versioned_ensembl_gene_id":"ENSG00000258312.1","gene_symbol":"AC016152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98113014,"end":98292445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170100.13","gene_symbol":"ZNF778","gene_name":"zinc finger protein 778 [Source:HGNC Symbol;Acc:HGNC:26479]","synonyms":"FLJ31875","biotype":"protein_coding","ncbi_id":"197320","summary":"The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]","start":89217703,"end":89237071,"strand":1,"description":"zinc finger protein 778 [Source:HGNC Symbol;Acc:HGNC:26479]"}, {"versioned_ensembl_gene_id":"ENSG00000254796.1","gene_symbol":"AC134684.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7601004,"end":7601267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255557.1","gene_symbol":"AP001266.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65745729,"end":65771585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225302.2","gene_symbol":"AC023283.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":116828761,"end":116850205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223442.1","gene_symbol":"TH2LCRR","gene_name":"T helper type 2 locus control region associated RNA [Source:HGNC Symbol;Acc:HGNC:40495]","synonyms":"TH2-LCR","biotype":"antisense_RNA","ncbi_id":"101927761","summary":null,"start":132630589,"end":132664272,"strand":-1,"description":"T helper type 2 locus control region associated RNA [Source:HGNC Symbol;Acc:HGNC:40495]"}, {"versioned_ensembl_gene_id":"ENSG00000104447.12","gene_symbol":"TRPS1","gene_name":"transcriptional repressor GATA binding 1 [Source:HGNC Symbol;Acc:HGNC:12340]","synonyms":"LGCR,GC79","biotype":"protein_coding","ncbi_id":"7227","summary":"This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [provided by RefSeq, Jul 2008]","start":115408496,"end":115809673,"strand":-1,"description":"transcriptional repressor GATA binding 1 [Source:HGNC Symbol;Acc:HGNC:12340]"}, {"versioned_ensembl_gene_id":"ENSG00000212721.3","gene_symbol":"KRTAP4-11","gene_name":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]","synonyms":"KAP4.11,KRTAP4-14,KAP4.14","biotype":"protein_coding","ncbi_id":"653240","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Mar 2009]","start":41117181,"end":41118360,"strand":-1,"description":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]"}, {"versioned_ensembl_gene_id":"ENSG00000112306.7","gene_symbol":"RPS12","gene_name":"ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10385]","synonyms":"S12","biotype":"protein_coding","ncbi_id":"6206","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S12E family of ribosomal proteins. It is located in the cytoplasm. Increased expression of this gene in colorectal cancers compared to matched normal colonic mucosa has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":132814441,"end":132817564,"strand":1,"description":"ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10385]"}, {"versioned_ensembl_gene_id":"ENSG00000167554.14","gene_symbol":"ZNF610","gene_name":"zinc finger protein 610 [Source:HGNC Symbol;Acc:HGNC:26687]","synonyms":"FLJ36040","biotype":"protein_coding","ncbi_id":"162963","summary":null,"start":52336245,"end":52367778,"strand":1,"description":"zinc finger protein 610 [Source:HGNC Symbol;Acc:HGNC:26687]"}, {"versioned_ensembl_gene_id":"ENSG00000269535.1","gene_symbol":"AC010320.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52300693,"end":52345229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270612.1","gene_symbol":"AC112191.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160326693,"end":160326969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172794.19","gene_symbol":"RAB37","gene_name":"RAB37, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"326624","summary":"Rab proteins are low molecular mass GTPases that are critical regulators of vesicle trafficking. For additional background information on Rab proteins, see MIM 179508.[supplied by OMIM, Apr 2006]","start":74670578,"end":74747335,"strand":1,"description":"RAB37, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30268]"}, {"versioned_ensembl_gene_id":"ENSG00000283246.1","gene_symbol":"MEP1AP1","gene_name":"meprin A subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7016]","synonyms":"MEP1AL1","biotype":"unprocessed_pseudogene","ncbi_id":"642840","summary":null,"start":40187792,"end":40193921,"strand":-1,"description":"meprin A subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7016]"}, {"versioned_ensembl_gene_id":"ENSG00000100906.10","gene_symbol":"NFKBIA","gene_name":"NFKB inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:7797]","synonyms":"NFKBI,MAD-3,IKBA,IkappaBalpha","biotype":"protein_coding","ncbi_id":"4792","summary":"This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011]","start":35401511,"end":35404749,"strand":-1,"description":"NFKB inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:7797]"}, {"versioned_ensembl_gene_id":"ENSG00000268536.1","gene_symbol":"AC005523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4785120,"end":4791207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214518.3","gene_symbol":"KRTAP2-2","gene_name":"keratin associated protein 2-2 [Source:HGNC Symbol;Acc:HGNC:18905]","synonyms":"KAP2.2","biotype":"protein_coding","ncbi_id":"728279","summary":null,"start":41054498,"end":41055230,"strand":-1,"description":"keratin associated protein 2-2 [Source:HGNC Symbol;Acc:HGNC:18905]"}, {"versioned_ensembl_gene_id":"ENSG00000176857.5","gene_symbol":"GJA1P1","gene_name":"gap junction protein alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4275]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"2698","summary":null,"start":109051315,"end":109052457,"strand":-1,"description":"gap junction protein alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4275]"}, {"versioned_ensembl_gene_id":"ENSG00000180422.3","gene_symbol":"LINC00304","gene_name":"long intergenic non-protein coding RNA 304 [Source:HGNC Symbol;Acc:HGNC:26713]","synonyms":"C16orf81,NCRNA00304,FLJ36701","biotype":"lincRNA","ncbi_id":"283860","summary":null,"start":89159146,"end":89164245,"strand":1,"description":"long intergenic non-protein coding RNA 304 [Source:HGNC Symbol;Acc:HGNC:26713]"}, {"versioned_ensembl_gene_id":"ENSG00000236966.1","gene_symbol":"AL773545.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40131747,"end":40132218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248654.1","gene_symbol":"MTCO3P44","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52147]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075289","summary":null,"start":25720516,"end":25721056,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52147]"}, {"versioned_ensembl_gene_id":"ENSG00000267024.1","gene_symbol":"AC008747.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34426112,"end":34428273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251353.1","gene_symbol":"MTND3P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42154]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873186","summary":null,"start":25720099,"end":25720431,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42154]"}, {"versioned_ensembl_gene_id":"ENSG00000248133.1","gene_symbol":"MTND4LP22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42256]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075102","summary":null,"start":25719755,"end":25720030,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42256]"}, {"versioned_ensembl_gene_id":"ENSG00000266953.6","gene_symbol":"AC092073.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34396315,"end":34409364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108262.15","gene_symbol":"GIT1","gene_name":"GIT ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:4272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28964","summary":null,"start":29573469,"end":29594054,"strand":-1,"description":"GIT ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:4272]"}, {"versioned_ensembl_gene_id":"ENSG00000198711.5","gene_symbol":"SSBP3-AS1","gene_name":"SSBP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32328]","synonyms":"MSTP128,C1orf191","biotype":"antisense_RNA","ncbi_id":"619518","summary":null,"start":54236440,"end":54239063,"strand":1,"description":"SSBP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32328]"}, {"versioned_ensembl_gene_id":"ENSG00000113312.10","gene_symbol":"TTC1","gene_name":"tetratricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12391]","synonyms":"TPR1","biotype":"protein_coding","ncbi_id":"7265","summary":"This gene encodes a protein that belongs to the tetratrico peptide repeat superfamily of proteins. The encoded protein plays a role in protein-protein interactions, and binds to the Galpha subunit of G protein-coupled receptors to activate the Ras signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":160009113,"end":160065543,"strand":1,"description":"tetratricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12391]"}, {"versioned_ensembl_gene_id":"ENSG00000165973.18","gene_symbol":"NELL1","gene_name":"neural EGFL like 1 [Source:HGNC Symbol;Acc:HGNC:7750]","synonyms":"IDH3GL,FLJ45906","biotype":"protein_coding","ncbi_id":"4745","summary":"This gene encodes a cytoplasmic protein that contains epidermal growth factor (EGF)-like repeats. The encoded heterotrimeric protein may be involved in cell growth regulation and differentiation. A similar protein in rodents is involved in craniosynostosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":20669551,"end":21575681,"strand":1,"description":"neural EGFL like 1 [Source:HGNC Symbol;Acc:HGNC:7750]"}, {"versioned_ensembl_gene_id":"ENSG00000196099.4","gene_symbol":"OR6M1","gene_name":"olfactory receptor family 6 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14711]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390261","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123805335,"end":123806387,"strand":-1,"description":"olfactory receptor family 6 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14711]"}, {"versioned_ensembl_gene_id":"ENSG00000267274.1","gene_symbol":"AC008770.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":11939959,"end":11953381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120068.6","gene_symbol":"HOXB8","gene_name":"homeobox B8 [Source:HGNC Symbol;Acc:HGNC:5119]","synonyms":"HOX2D,HOX2","biotype":"protein_coding","ncbi_id":"3218","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with colorectal cancer. Mice that have had the murine ortholog of this gene knocked out exhibit an excessive pathologic grooming behavior. This behavior is similar to the behavior of humans suffering from the obsessive-compulsive spectrum disorder trichotillomania. [provided by RefSeq, Jul 2008]","start":48611377,"end":48614939,"strand":-1,"description":"homeobox B8 [Source:HGNC Symbol;Acc:HGNC:5119]"}, {"versioned_ensembl_gene_id":"ENSG00000227962.1","gene_symbol":"AL391994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235336806,"end":235337087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235025.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"RFB30,HERF1,RNF9","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30197074,"end":30206062,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000234442.4","gene_symbol":"BX276092.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71760764,"end":71763075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158457.5","gene_symbol":"TSPAN33","gene_name":"tetraspanin 33 [Source:HGNC Symbol;Acc:HGNC:28743]","synonyms":"Penumbra,MGC50844","biotype":"protein_coding","ncbi_id":"340348","summary":null,"start":129144892,"end":129169697,"strand":1,"description":"tetraspanin 33 [Source:HGNC Symbol;Acc:HGNC:28743]"}, {"versioned_ensembl_gene_id":"ENSG00000261845.2","gene_symbol":"AC124283.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82602989,"end":82604178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101977.19","gene_symbol":"MCF2","gene_name":"MCF.2 cell line derived transforming sequence [Source:HGNC Symbol;Acc:HGNC:6940]","synonyms":"DBL,ARHGEF21","biotype":"protein_coding","ncbi_id":"4168","summary":"The oncogenic protein encoded by this gene is a guanine nucleotide exchange factor (GEF) that exerts control over some members of the Rho family of small GTPases. Several transcript variants encoding different isoforms have been found for this gene. These isoforms exhibit different expression patterns and varying levels of GEF activity.[provided by RefSeq, Jan 2010]","start":139581770,"end":139708227,"strand":-1,"description":"MCF.2 cell line derived transforming sequence [Source:HGNC Symbol;Acc:HGNC:6940]"}, {"versioned_ensembl_gene_id":"ENSG00000120738.7","gene_symbol":"EGR1","gene_name":"early growth response 1 [Source:HGNC Symbol;Acc:HGNC:3238]","synonyms":"ZNF225,ZIF-268,TIS8,NGFI-A,KROX-24,G0S30,AT225","biotype":"protein_coding","ncbi_id":"1958","summary":"The protein encoded by this gene belongs to the EGR family of C2H2-type zinc-finger proteins. It is a nuclear protein and functions as a transcriptional regulator. The products of target genes it activates are required for differentitation and mitogenesis. Studies suggest this is a cancer suppressor gene. [provided by RefSeq, Dec 2014]","start":138465490,"end":138469315,"strand":1,"description":"early growth response 1 [Source:HGNC Symbol;Acc:HGNC:3238]"}, {"versioned_ensembl_gene_id":"ENSG00000215115.6","gene_symbol":"CXorf49","gene_name":"chromosome X open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:30891]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130361","summary":null,"start":71714371,"end":71718151,"strand":-1,"description":"chromosome X open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:30891]"}, {"versioned_ensembl_gene_id":"ENSG00000253638.1","gene_symbol":"AF186190.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133392211,"end":133392690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284601.1","gene_symbol":"AL590440.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":54974900,"end":54980464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237447.1","gene_symbol":"CDC27P2","gene_name":"cell division cycle 27 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38092]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130277","summary":null,"start":10190377,"end":10192298,"strand":-1,"description":"cell division cycle 27 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38092]"}, {"versioned_ensembl_gene_id":"ENSG00000141568.20","gene_symbol":"FOXK2","gene_name":"forkhead box K2 [Source:HGNC Symbol;Acc:HGNC:6036]","synonyms":"ILF1,ILF","biotype":"protein_coding","ncbi_id":"3607","summary":"The protein encoded by this gene contains a fork head DNA binding domain. This protein can bind to the purine-rich motifs of the HIV long terminal repeat (LTR), and to the similar purine-rich motif in the interleukin 2 (IL2) promoter. It may be involved in the regulation of viral and cellular promoter elements. [provided by RefSeq, Jul 2008]","start":82519713,"end":82644662,"strand":1,"description":"forkhead box K2 [Source:HGNC Symbol;Acc:HGNC:6036]"}, {"versioned_ensembl_gene_id":"ENSG00000136802.11","gene_symbol":"LRRC8A","gene_name":"leucine rich repeat containing 8 family member A [Source:HGNC Symbol;Acc:HGNC:19027]","synonyms":"SWELL1,LRRC8,KIAA1437,FLJ10337","biotype":"protein_coding","ncbi_id":"56262","summary":"This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":128882112,"end":128918039,"strand":1,"description":"leucine rich repeat containing 8 family member A [Source:HGNC Symbol;Acc:HGNC:19027]"}, {"versioned_ensembl_gene_id":"ENSG00000283376.1","gene_symbol":"AC011591.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":68691809,"end":68716064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266222.1","gene_symbol":"AC036222.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48377262,"end":48380370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216516.1","gene_symbol":"AL645733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160163539,"end":160163755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256195.2","gene_symbol":"AP002518.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114360635,"end":114380045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141753.6","gene_symbol":"IGFBP4","gene_name":"insulin like growth factor binding protein 4 [Source:HGNC Symbol;Acc:HGNC:5473]","synonyms":"HT29-IGFBP,BP-4,IGFBP-4,IBP4","biotype":"protein_coding","ncbi_id":"3487","summary":"This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP domain and a thyroglobulin type-I domain. The protein binds both insulin-like growth factors (IGFs) I and II and circulates in the plasma in both glycosylated and non-glycosylated forms. Binding of this protein prolongs the half-life of the IGFs and alters their interaction with cell surface receptors. [provided by RefSeq, Jul 2008]","start":40443461,"end":40457731,"strand":1,"description":"insulin like growth factor binding protein 4 [Source:HGNC Symbol;Acc:HGNC:5473]"}, {"versioned_ensembl_gene_id":"ENSG00000204897.6","gene_symbol":"KRT25","gene_name":"keratin 25 [Source:HGNC Symbol;Acc:HGNC:30839]","synonyms":"KRT25A","biotype":"protein_coding","ncbi_id":"147183","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40748021,"end":40755332,"strand":-1,"description":"keratin 25 [Source:HGNC Symbol;Acc:HGNC:30839]"}, {"versioned_ensembl_gene_id":"ENSG00000255184.1","gene_symbol":"AP004607.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90017611,"end":90024511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278338.4","gene_symbol":"VWA8-AS1","gene_name":"VWA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44270]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507240","summary":null,"start":41955808,"end":41981565,"strand":1,"description":"VWA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44270]"}, {"versioned_ensembl_gene_id":"ENSG00000223546.6","gene_symbol":"LINC00630","gene_name":"long intergenic non-protein coding RNA 630 [Source:HGNC Symbol;Acc:HGNC:44263]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287765","summary":null,"start":102769161,"end":102885406,"strand":1,"description":"long intergenic non-protein coding RNA 630 [Source:HGNC Symbol;Acc:HGNC:44263]"}, {"versioned_ensembl_gene_id":"ENSG00000232282.1","gene_symbol":"MTND1P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100856881","summary":null,"start":102785667,"end":102786604,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42081]"}, {"versioned_ensembl_gene_id":"ENSG00000235138.1","gene_symbol":"AL445931.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134054290,"end":134058805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280093.1","gene_symbol":"AP002791.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91382909,"end":91383289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250126.1","gene_symbol":"AC116563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137645265,"end":137655174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251632.1","gene_symbol":"LINC02172","gene_name":"long intergenic non-protein coding RNA 2172 [Source:HGNC Symbol;Acc:HGNC:53034]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377443","summary":null,"start":137545731,"end":137603430,"strand":1,"description":"long intergenic non-protein coding RNA 2172 [Source:HGNC Symbol;Acc:HGNC:53034]"}, {"versioned_ensembl_gene_id":"ENSG00000225826.1","gene_symbol":"LINC00626","gene_name":"long intergenic non-protein coding RNA 626 [Source:HGNC Symbol;Acc:HGNC:44257]","synonyms":"MGC4473","biotype":"lincRNA","ncbi_id":"79100","summary":null,"start":168786939,"end":168792886,"strand":1,"description":"long intergenic non-protein coding RNA 626 [Source:HGNC Symbol;Acc:HGNC:44257]"}, {"versioned_ensembl_gene_id":"ENSG00000230702.1","gene_symbol":"AC107081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61856695,"end":61857055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108946.14","gene_symbol":"PRKAR1A","gene_name":"protein kinase cAMP-dependent type I regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9388]","synonyms":"TSE1,PRKAR1,CNC1","biotype":"protein_coding","ncbi_id":"5573","summary":"cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. This gene encodes one of the regulatory subunits. This protein was found to be a tissue-specific extinguisher that down-regulates the expression of seven liver genes in hepatoma x fibroblast hybrids. Mutations in this gene cause Carney complex (CNC). This gene can fuse to the RET protooncogene by gene rearrangement and form the thyroid tumor-specific chimeric oncogene known as PTC2. A nonconventional nuclear localization sequence (NLS) has been found for this protein which suggests a role in DNA replication via the protein serving as a nuclear transport protein for the second subunit of the Replication Factor C (RFC40). Several alternatively spliced transcript variants encoding two different isoforms have been observed. [provided by RefSeq, Jan 2013]","start":68511780,"end":68551319,"strand":1,"description":"protein kinase cAMP-dependent type I regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9388]"}, {"versioned_ensembl_gene_id":"ENSG00000002919.14","gene_symbol":"SNX11","gene_name":"sorting nexin 11 [Source:HGNC Symbol;Acc:HGNC:14975]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29916","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene encodes a protein of unknown function. This gene results in two transcript variants differing in the 5' UTR, but encoding the same protein. [provided by RefSeq, Jul 2008]","start":48103357,"end":48123074,"strand":1,"description":"sorting nexin 11 [Source:HGNC Symbol;Acc:HGNC:14975]"}, {"versioned_ensembl_gene_id":"ENSG00000159199.13","gene_symbol":"ATP5G1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:841]","synonyms":"ATP5G","biotype":"protein_coding","ncbi_id":"516","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":48892765,"end":48895871,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:841]"}, {"versioned_ensembl_gene_id":"ENSG00000258823.1","gene_symbol":"AL160314.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22723476,"end":22726572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111788.10","gene_symbol":"AC009533.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9277235,"end":9313241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147416.10","gene_symbol":"ATP6V1B2","gene_name":"ATPase H+ transporting V1 subunit B2 [Source:HGNC Symbol;Acc:HGNC:854]","synonyms":"ATP6B2,VPP3,Vma2,VATB,HO57","biotype":"protein_coding","ncbi_id":"526","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. The protein encoded by this gene is one of two V1 domain B subunit isoforms and is the only B isoform highly expressed in osteoclasts. [provided by RefSeq, Jul 2008]","start":20197367,"end":20226819,"strand":1,"description":"ATPase H+ transporting V1 subunit B2 [Source:HGNC Symbol;Acc:HGNC:854]"}, {"versioned_ensembl_gene_id":"ENSG00000230415.1","gene_symbol":"LINC01786","gene_name":"long intergenic non-protein coding RNA 1786 [Source:HGNC Symbol;Acc:HGNC:52575]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928895","summary":null,"start":1275223,"end":1280420,"strand":1,"description":"long intergenic non-protein coding RNA 1786 [Source:HGNC Symbol;Acc:HGNC:52575]"}, {"versioned_ensembl_gene_id":"ENSG00000255804.2","gene_symbol":"OR6J1","gene_name":"olfactory receptor family 6 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14707]","synonyms":"OR6J2,OR6J1P","biotype":"polymorphic_pseudogene","ncbi_id":"79549","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":22630929,"end":22644352,"strand":-1,"description":"olfactory receptor family 6 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14707]"}, {"versioned_ensembl_gene_id":"ENSG00000265664.1","gene_symbol":"AC005544.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67032409,"end":67033290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259715.1","gene_symbol":"AC022087.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50359450,"end":50360194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203733.5","gene_symbol":"GJE1","gene_name":"gap junction protein epsilon 1 [Source:HGNC Symbol;Acc:HGNC:33251]","synonyms":"CX23","biotype":"protein_coding","ncbi_id":"100126572","summary":null,"start":142133090,"end":142135151,"strand":1,"description":"gap junction protein epsilon 1 [Source:HGNC Symbol;Acc:HGNC:33251]"}, {"versioned_ensembl_gene_id":"ENSG00000224729.5","gene_symbol":"PCOLCE-AS1","gene_name":"PCOLCE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40430]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129845","summary":null,"start":100589402,"end":100604206,"strand":-1,"description":"PCOLCE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40430]"}, {"versioned_ensembl_gene_id":"ENSG00000246067.7","gene_symbol":"RAB30-AS1","gene_name":"RAB30 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48672]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506233","summary":null,"start":83072066,"end":83106719,"strand":1,"description":"RAB30 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48672]"}, {"versioned_ensembl_gene_id":"ENSG00000180613.10","gene_symbol":"GSX2","gene_name":"GS homeobox 2 [Source:HGNC Symbol;Acc:HGNC:24959]","synonyms":"Gsh2","biotype":"protein_coding","ncbi_id":"170825","summary":null,"start":54099523,"end":54102505,"strand":1,"description":"GS homeobox 2 [Source:HGNC Symbol;Acc:HGNC:24959]"}, {"versioned_ensembl_gene_id":"ENSG00000255503.1","gene_symbol":"AP001767.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83072402,"end":83097196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183122.5","gene_symbol":"OR2A3P","gene_name":"olfactory receptor family 2 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8231]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"202861","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144153486,"end":144158905,"strand":1,"description":"olfactory receptor family 2 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8231]"}, {"versioned_ensembl_gene_id":"ENSG00000221938.5","gene_symbol":"OR2A14","gene_name":"olfactory receptor family 2 subfamily A member 14 [Source:HGNC Symbol;Acc:HGNC:15084]","synonyms":"OST182,OR2A6,OR2A14P","biotype":"protein_coding","ncbi_id":"135941","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144123176,"end":144131188,"strand":1,"description":"olfactory receptor family 2 subfamily A member 14 [Source:HGNC Symbol;Acc:HGNC:15084]"}, {"versioned_ensembl_gene_id":"ENSG00000243303.1","gene_symbol":"AC103987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21854640,"end":21854987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277426.1","gene_symbol":"AC006441.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39023394,"end":39026742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136930.12","gene_symbol":"PSMB7","gene_name":"proteasome subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:9544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5695","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. The encoded protein is a member of the proteasome B-type family, also known as the T1B family, and is a 20S core beta subunit in the proteasome. Expression of this catalytic subunit is downregulated by gamma interferon, and proteolytic processing is required to generate a mature subunit. A pseudogene of this gene is located on the long arm of chromosome 14. [provided by RefSeq, Jul 2012]","start":124353466,"end":124415444,"strand":-1,"description":"proteasome subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:9544]"}, {"versioned_ensembl_gene_id":"ENSG00000002834.17","gene_symbol":"LASP1","gene_name":"LIM and SH3 protein 1 [Source:HGNC Symbol;Acc:HGNC:6513]","synonyms":"MLN50,Lasp-1","biotype":"protein_coding","ncbi_id":"3927","summary":"This gene encodes a member of a subfamily of LIM proteins, characterized by a LIM motif and a domain of Src homology region 3, and also a member of the nebulin family of actin-binding proteins. The encoded protein is a cAMP and cGMP dependent signaling protein and binds to the actin cytoskeleton at extensions of the cell membrane. The encoded protein has been linked to metastatic breast cancer, hematopoetic tumors such as B-cell lymphomas, and colorectal cancer. [provided by RefSeq, Oct 2012]","start":38869859,"end":38921770,"strand":1,"description":"LIM and SH3 protein 1 [Source:HGNC Symbol;Acc:HGNC:6513]"}, {"versioned_ensembl_gene_id":"ENSG00000235128.1","gene_symbol":"AC013474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126679622,"end":126680420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234397.3","gene_symbol":"AL591122.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22322840,"end":22323331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253422.1","gene_symbol":"AC008677.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158078099,"end":158078764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223427.1","gene_symbol":"AC016716.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80162428,"end":80163135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213414.3","gene_symbol":"AC008677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157986146,"end":157987706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188001.9","gene_symbol":"TPRG1","gene_name":"tumor protein p63 regulated 1 [Source:HGNC Symbol;Acc:HGNC:24759]","synonyms":"FAM79B,FLJ43694,FLJ41238","biotype":"protein_coding","ncbi_id":"285386","summary":null,"start":188947214,"end":189325304,"strand":1,"description":"tumor protein p63 regulated 1 [Source:HGNC Symbol;Acc:HGNC:24759]"}, {"versioned_ensembl_gene_id":"ENSG00000236182.1","gene_symbol":"AC009319.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188989382,"end":188990135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143155.12","gene_symbol":"TIPRL","gene_name":"TOR signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:30231]","synonyms":"TIPRL1,TIP41,MGC3794,dJ69E11.3","biotype":"protein_coding","ncbi_id":"261726","summary":"TIPRL is an inhibitory regulator of protein phosphatase-2A (PP2A) (see PPP2CA; MIM 176915), PP4 (see PPP4C; MIM 602035), and PP6 (see PPP6C; MIM 612725) (McConnell et al., 2007 [PubMed 17384681]).[supplied by OMIM, Nov 2010]","start":168178933,"end":168202114,"strand":1,"description":"TOR signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:30231]"}, {"versioned_ensembl_gene_id":"ENSG00000258830.1","gene_symbol":"AC137834.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57249609,"end":57296484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282760.1","gene_symbol":"TRBV12-1","gene_name":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]","synonyms":"TCRBV8S4P,TCRBV12S1,TRBV121","biotype":"TR_V_pseudogene","ncbi_id":"28579","summary":null,"start":142436931,"end":142437373,"strand":1,"description":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]"}, {"versioned_ensembl_gene_id":"ENSG00000249840.2","gene_symbol":"GAPDHP76","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:50649]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287725","summary":null,"start":11585246,"end":11587135,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:50649]"}, {"versioned_ensembl_gene_id":"ENSG00000242255.1","gene_symbol":"RPL39P34","gene_name":"ribosomal protein L39 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36528]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100271523","summary":null,"start":52564076,"end":52564231,"strand":1,"description":"ribosomal protein L39 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36528]"}, {"versioned_ensembl_gene_id":"ENSG00000145425.9","gene_symbol":"RPS3A","gene_name":"ribosomal protein S3A [Source:HGNC Symbol;Acc:HGNC:10421]","synonyms":"S3A,MFTL","biotype":"protein_coding","ncbi_id":"6189","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S3AE family of ribosomal proteins. It is located in the cytoplasm. Disruption of the gene encoding rat ribosomal protein S3a, also named v-fos transformation effector protein, in v-fos-transformed rat cells results in reversion of the transformed phenotype. This gene is co-transcribed with the U73A and U73B small nucleolar RNA genes, which are located in its fourth and third introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]","start":151099573,"end":151104652,"strand":1,"description":"ribosomal protein S3A [Source:HGNC Symbol;Acc:HGNC:10421]"}, {"versioned_ensembl_gene_id":"ENSG00000226497.1","gene_symbol":"LINC02549","gene_name":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928280","summary":null,"start":68226972,"end":68329899,"strand":-1,"description":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]"}, {"versioned_ensembl_gene_id":"ENSG00000229385.1","gene_symbol":"AC010975.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79493716,"end":79500844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250350.1","gene_symbol":"AC104819.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151279030,"end":151279192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230237.1","gene_symbol":"AC010975.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79573764,"end":79575593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224023.10","gene_symbol":"FLJ37035","gene_name":"uncharacterized LOC399821 [Source:NCBI gene;Acc:399821]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399821","summary":null,"start":125700436,"end":125719566,"strand":-1,"description":"uncharacterized LOC399821 [Source:NCBI gene;Acc:399821]"}, {"versioned_ensembl_gene_id":"ENSG00000162337.11","gene_symbol":"LRP5","gene_name":"LDL receptor related protein 5 [Source:HGNC Symbol;Acc:HGNC:6697]","synonyms":"EVR4,EVR1,BMND1,VBCH2,OPTA1,OPS,OPPG,LRP7,LR3,HBM","biotype":"protein_coding","ncbi_id":"4041","summary":"This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":68312609,"end":68449275,"strand":1,"description":"LDL receptor related protein 5 [Source:HGNC Symbol;Acc:HGNC:6697]"}, {"versioned_ensembl_gene_id":"ENSG00000276033.4","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"FLJ00060,LENG12","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54463149,"end":54476118,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000253541.1","gene_symbol":"SEPT10P1","gene_name":"septin 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389662","summary":null,"start":56476826,"end":56477987,"strand":-1,"description":"septin 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40018]"}, {"versioned_ensembl_gene_id":"ENSG00000230408.3","gene_symbol":"AC007163.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":200780495,"end":200812170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203805.10","gene_symbol":"PLPP4","gene_name":"phospholipid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:23531]","synonyms":"PPAPDC1A,PPAPDC1,DPPL2","biotype":"protein_coding","ncbi_id":"196051","summary":null,"start":120456954,"end":120589855,"strand":1,"description":"phospholipid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:23531]"}, {"versioned_ensembl_gene_id":"ENSG00000127585.11","gene_symbol":"FBXL16","gene_name":"F-box and leucine rich repeat protein 16 [Source:HGNC Symbol;Acc:HGNC:14150]","synonyms":"MGC33974,Fbl16,C16orf22","biotype":"protein_coding","ncbi_id":"146330","summary":"Members of the F-box protein family, such as FBXL16, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":692498,"end":705829,"strand":-1,"description":"F-box and leucine rich repeat protein 16 [Source:HGNC Symbol;Acc:HGNC:14150]"}, {"versioned_ensembl_gene_id":"ENSG00000211886.1","gene_symbol":"TRAJ3","gene_name":"T-cell receptor alpha joining 3 [Source:HGNC Symbol;Acc:HGNC:12059]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28752","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22543179,"end":22543240,"strand":1,"description":"T-cell receptor alpha joining 3 [Source:HGNC Symbol;Acc:HGNC:12059]"}, {"versioned_ensembl_gene_id":"ENSG00000283428.1","gene_symbol":"CCDC195","gene_name":"coiled-coil domain containing 195 [Source:HGNC Symbol;Acc:HGNC:53441]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":224703764,"end":224716365,"strand":-1,"description":"coiled-coil domain containing 195 [Source:HGNC Symbol;Acc:HGNC:53441]"}, {"versioned_ensembl_gene_id":"ENSG00000231491.2","gene_symbol":"JKAMPP1","gene_name":"JNK1/MAPK8-associated membrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100049717","summary":null,"start":12287320,"end":12288238,"strand":1,"description":"JNK1/MAPK8-associated membrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49759]"}, {"versioned_ensembl_gene_id":"ENSG00000251440.2","gene_symbol":"STMN1P2","gene_name":"stathmin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44063]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289663","summary":null,"start":137425426,"end":137425864,"strand":-1,"description":"stathmin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44063]"}, {"versioned_ensembl_gene_id":"ENSG00000211884.1","gene_symbol":"TRAJ5","gene_name":"T-cell receptor alpha joining 5 [Source:HGNC Symbol;Acc:HGNC:12081]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28750","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22540247,"end":22540306,"strand":1,"description":"T-cell receptor alpha joining 5 [Source:HGNC Symbol;Acc:HGNC:12081]"}, {"versioned_ensembl_gene_id":"ENSG00000211883.1","gene_symbol":"TRAJ6","gene_name":"T-cell receptor alpha joining 6 [Source:HGNC Symbol;Acc:HGNC:12092]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28749","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22539073,"end":22539134,"strand":1,"description":"T-cell receptor alpha joining 6 [Source:HGNC Symbol;Acc:HGNC:12092]"}, {"versioned_ensembl_gene_id":"ENSG00000224342.1","gene_symbol":"AC007879.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207173634,"end":207222790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180230.6","gene_symbol":"NACAP2","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651144","summary":null,"start":119997086,"end":119997709,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49489]"}, {"versioned_ensembl_gene_id":"ENSG00000282493.1","gene_symbol":"AC100810.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1757770,"end":1760009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211872.1","gene_symbol":"TRAJ17","gene_name":"T-cell receptor alpha joining 17 [Source:HGNC Symbol;Acc:HGNC:12045]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28738","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22526844,"end":22526906,"strand":1,"description":"T-cell receptor alpha joining 17 [Source:HGNC Symbol;Acc:HGNC:12045]"}, {"versioned_ensembl_gene_id":"ENSG00000129116.17","gene_symbol":"PALLD","gene_name":"palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:HGNC:17068]","synonyms":"SIH002,KIAA0992,CGI-151","biotype":"protein_coding","ncbi_id":"23022","summary":"This gene encodes a cytoskeletal protein that is required for organizing the actin cytoskeleton. The protein is a component of actin-containing microfilaments, and it is involved in the control of cell shape, adhesion, and contraction. Polymorphisms in this gene are associated with a susceptibility to pancreatic cancer type 1, and also with a risk for myocardial infarction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":168497066,"end":168928457,"strand":1,"description":"palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:HGNC:17068]"}, {"versioned_ensembl_gene_id":"ENSG00000166922.8","gene_symbol":"SCG5","gene_name":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]","synonyms":"7B2,SgV,SGNE1,7B2,SgV,SGNE1","biotype":"protein_coding","ncbi_id":"6447","summary":"This gene encodes a secreted chaperone protein that prevents the aggregation of other secreted proteins, including proteins that are associated with neurodegenerative and metabolic disease. The encoded protein may be best known for its role in the trafficking and activation of prohormone convertase PC2 (encoded by Gene ID: 5126). Phosphorylation of the encoded protein has been shown to have an inhibitory effect on its chaperone function. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32641676,"end":32697098,"strand":1,"description":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]"}, {"versioned_ensembl_gene_id":"ENSG00000162552.14","gene_symbol":"WNT4","gene_name":"Wnt family member 4 [Source:HGNC Symbol;Acc:HGNC:12783]","synonyms":"WNT-4","biotype":"protein_coding","ncbi_id":"54361","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family, and is the first signaling molecule shown to influence the sex-determination cascade. It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat. This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation. This gene and another two family members, WNT2 and WNT7B, may be associated with abnormal proliferation in breast tissue. Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome. [provided by RefSeq, Jul 2008]","start":22117305,"end":22143969,"strand":-1,"description":"Wnt family member 4 [Source:HGNC Symbol;Acc:HGNC:12783]"}, {"versioned_ensembl_gene_id":"ENSG00000211861.1","gene_symbol":"TRAJ28","gene_name":"T-cell receptor alpha joining 28 [Source:HGNC Symbol;Acc:HGNC:12057]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28727","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22515623,"end":22515688,"strand":1,"description":"T-cell receptor alpha joining 28 [Source:HGNC Symbol;Acc:HGNC:12057]"}, {"versioned_ensembl_gene_id":"ENSG00000249875.1","gene_symbol":"AC116616.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174354854,"end":174376445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268289.1","gene_symbol":"AC020908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17051994,"end":17055087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104044.15","gene_symbol":"OCA2","gene_name":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]","synonyms":"EYCL,D15S12,BEY2,BEY1,BEY,P,EYCL3,EYCL2","biotype":"protein_coding","ncbi_id":"4948","summary":"This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":27754875,"end":28099358,"strand":-1,"description":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]"}, {"versioned_ensembl_gene_id":"ENSG00000103852.12","gene_symbol":"TTC23","gene_name":"tetratricopeptide repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:25730]","synonyms":"HCC-8,FLJ12572","biotype":"protein_coding","ncbi_id":"64927","summary":null,"start":99136323,"end":99251223,"strand":-1,"description":"tetratricopeptide repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:25730]"}, {"versioned_ensembl_gene_id":"ENSG00000214297.3","gene_symbol":"ALDOAP2","gene_name":"aldolase, fructose-bisphosphate A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:416]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"228","summary":null,"start":125666875,"end":125667950,"strand":-1,"description":"aldolase, fructose-bisphosphate A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:416]"}, {"versioned_ensembl_gene_id":"ENSG00000211856.1","gene_symbol":"TRAJ33","gene_name":"T-cell receptor alpha joining 33 [Source:HGNC Symbol;Acc:HGNC:12063]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28722","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22508602,"end":22508658,"strand":1,"description":"T-cell receptor alpha joining 33 [Source:HGNC Symbol;Acc:HGNC:12063]"}, {"versioned_ensembl_gene_id":"ENSG00000255295.1","gene_symbol":"AP002404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89498748,"end":89499198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261078.1","gene_symbol":"AC009118.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58382989,"end":58383798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012124.16","gene_symbol":"CD22","gene_name":"CD22 molecule [Source:HGNC Symbol;Acc:HGNC:1643]","synonyms":"SIGLEC2,SIGLEC-2","biotype":"protein_coding","ncbi_id":"933","summary":null,"start":35319261,"end":35347355,"strand":1,"description":"CD22 molecule [Source:HGNC Symbol;Acc:HGNC:1643]"}, {"versioned_ensembl_gene_id":"ENSG00000132718.8","gene_symbol":"SYT11","gene_name":"synaptotagmin 11 [Source:HGNC Symbol;Acc:HGNC:19239]","synonyms":"MGC17226,MGC10881,KIAA0080,DKFZp781D015","biotype":"protein_coding","ncbi_id":"23208","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that are known calcium sensors and mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. The encoded protein is also a substrate for ubiquitin-E3-ligase parkin. The gene has previously been referred to as synaptotagmin XII but has been renamed synaptotagmin XI to be consistent with mouse and rat official nomenclature. [provided by RefSeq, Apr 2010]","start":155859509,"end":155885199,"strand":1,"description":"synaptotagmin 11 [Source:HGNC Symbol;Acc:HGNC:19239]"}, {"versioned_ensembl_gene_id":"ENSG00000183260.7","gene_symbol":"ABHD16B","gene_name":"abhydrolase domain containing 16B [Source:HGNC Symbol;Acc:HGNC:16128]","synonyms":"dJ591C20.1,C20orf135","biotype":"protein_coding","ncbi_id":"140701","summary":null,"start":63861498,"end":63862988,"strand":1,"description":"abhydrolase domain containing 16B [Source:HGNC Symbol;Acc:HGNC:16128]"}, {"versioned_ensembl_gene_id":"ENSG00000206140.10","gene_symbol":"TMEM191C","gene_name":"transmembrane protein 191C [Source:HGNC Symbol;Acc:HGNC:33601]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645426","summary":null,"start":21466423,"end":21471269,"strand":1,"description":"transmembrane protein 191C [Source:HGNC Symbol;Acc:HGNC:33601]"}, {"versioned_ensembl_gene_id":"ENSG00000217684.2","gene_symbol":"RPS3AP24","gene_name":"ribosomal protein S3a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36267]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271253","summary":null,"start":140761529,"end":140762262,"strand":1,"description":"ribosomal protein S3a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36267]"}, {"versioned_ensembl_gene_id":"ENSG00000236031.1","gene_symbol":"AL591721.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":243545532,"end":243548329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269814.1","gene_symbol":"AC008403.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48513207,"end":48513660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108825.17","gene_symbol":"PTGES3L-AARSD1","gene_name":"PTGES3L-AARSD1 readthrough [Source:HGNC Symbol;Acc:HGNC:43946]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100885850","summary":"This locus represents naturally occurring readthrough transcription between the neighboring PTGES3L (prostaglandin E synthase 3 (cytosolic)-like) and AARSD1(alanyl-tRNA synthetase domain containing 1) genes on chromosome 17. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, May 2012]","start":42950526,"end":42980528,"strand":-1,"description":"PTGES3L-AARSD1 readthrough [Source:HGNC Symbol;Acc:HGNC:43946]"}, {"versioned_ensembl_gene_id":"ENSG00000211837.1","gene_symbol":"TRAJ53","gene_name":"T-cell receptor alpha joining 53 [Source:HGNC Symbol;Acc:HGNC:12085]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28702","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22483004,"end":22483069,"strand":1,"description":"T-cell receptor alpha joining 53 [Source:HGNC Symbol;Acc:HGNC:12085]"}, {"versioned_ensembl_gene_id":"ENSG00000104419.14","gene_symbol":"NDRG1","gene_name":"N-myc downstream regulated 1 [Source:HGNC Symbol;Acc:HGNC:7679]","synonyms":"TDD5,RTP,NDR1,DRG1,CAP43","biotype":"protein_coding","ncbi_id":"10397","summary":"This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. The encoded protein is necessary for p53-mediated caspase activation and apoptosis. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4D, and expression of this gene may be a prognostic indicator for several types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":133237171,"end":133302022,"strand":-1,"description":"N-myc downstream regulated 1 [Source:HGNC Symbol;Acc:HGNC:7679]"}, {"versioned_ensembl_gene_id":"ENSG00000254277.1","gene_symbol":"AC009446.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71675300,"end":71702786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235962.5","gene_symbol":"RPL7AP53","gene_name":"ribosomal protein L7a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36392]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401640","summary":null,"start":33057615,"end":33058407,"strand":-1,"description":"ribosomal protein L7a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36392]"}, {"versioned_ensembl_gene_id":"ENSG00000127955.15","gene_symbol":"GNAI1","gene_name":"G protein subunit alpha i1 [Source:HGNC Symbol;Acc:HGNC:4384]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2770","summary":"Guanine nucleotide binding proteins are heterotrimeric signal-transducing molecules consisting of alpha, beta, and gamma subunits. The alpha subunit binds guanine nucleotide, can hydrolyze GTP, and can interact with other proteins. The protein encoded by this gene represents the alpha subunit of an inhibitory complex. The encoded protein is part of a complex that responds to beta-adrenergic signals by inhibiting adenylate cyclase. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":80133955,"end":80219402,"strand":1,"description":"G protein subunit alpha i1 [Source:HGNC Symbol;Acc:HGNC:4384]"}, {"versioned_ensembl_gene_id":"ENSG00000235077.1","gene_symbol":"AC073842.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100130964,"end":100140439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229496.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"D6S81E,BAT1,UAP56","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31606569,"end":31622924,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000211812.1","gene_symbol":"TRAV26-2","gene_name":"T-cell receptor alpha variable 26-2 [Source:HGNC Symbol;Acc:HGNC:12124]","synonyms":"TRAV262,TCRAV4S1,TCRAV26S2","biotype":"TR_V_gene","ncbi_id":"28656","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22202583,"end":22203368,"strand":1,"description":"T-cell receptor alpha variable 26-2 [Source:HGNC Symbol;Acc:HGNC:12124]"}, {"versioned_ensembl_gene_id":"ENSG00000254859.1","gene_symbol":"AC067930.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143541973,"end":143549729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166401.14","gene_symbol":"SERPINB8","gene_name":"serpin family B member 8 [Source:HGNC Symbol;Acc:HGNC:8952]","synonyms":"PI8,CAP2","biotype":"protein_coding","ncbi_id":"5271","summary":"The protein encoded by this gene is a member of the ov-serpin family of serine protease inhibitors. The encoded protein is produced by platelets and can bind to and inhibit the function of furin, a serine protease involved in platelet functions. In addition, this protein has been found to enhance the mechanical stability of cell-cell adhesion in the skin, and defects in this gene have been associated with an autosomal-recessive form of exfoliative ichthyosis. [provided by RefSeq, Jan 2017]","start":63969925,"end":64019779,"strand":1,"description":"serpin family B member 8 [Source:HGNC Symbol;Acc:HGNC:8952]"}, {"versioned_ensembl_gene_id":"ENSG00000176563.9","gene_symbol":"CNTD1","gene_name":"cyclin N-terminal domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26847]","synonyms":"FLJ40137,CNTD","biotype":"protein_coding","ncbi_id":"124817","summary":null,"start":42798792,"end":42811587,"strand":1,"description":"cyclin N-terminal domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26847]"}, {"versioned_ensembl_gene_id":"ENSG00000176986.15","gene_symbol":"SEC24C","gene_name":"SEC24 homolog C, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10705]","synonyms":"KIAA0079","biotype":"protein_coding","ncbi_id":"9632","summary":"The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The product of this gene may play a role in shaping the vesicle, as well as in cargo selection and concentration. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":73744384,"end":73772161,"strand":1,"description":"SEC24 homolog C, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10705]"}, {"versioned_ensembl_gene_id":"ENSG00000090975.12","gene_symbol":"PITPNM2","gene_name":"phosphatidylinositol transfer protein membrane associated 2 [Source:HGNC Symbol;Acc:HGNC:21044]","synonyms":"RDGBA2,RDGB2,NIR3","biotype":"protein_coding","ncbi_id":"57605","summary":"PITPNM2 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]","start":122983480,"end":123150015,"strand":-1,"description":"phosphatidylinositol transfer protein membrane associated 2 [Source:HGNC Symbol;Acc:HGNC:21044]"}, {"versioned_ensembl_gene_id":"ENSG00000255239.1","gene_symbol":"TREHP1","gene_name":"trehalase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51907]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"768086","summary":null,"start":118688039,"end":118690600,"strand":-1,"description":"trehalase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51907]"}, {"versioned_ensembl_gene_id":"ENSG00000128272.14","gene_symbol":"ATF4","gene_name":"activating transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:786]","synonyms":"TXREB,TAXREB67,CREB-2","biotype":"protein_coding","ncbi_id":"468","summary":"This gene encodes a transcription factor that was originally identified as a widely expressed mammalian DNA binding protein that could bind a tax-responsive enhancer element in the LTR of HTLV-1. The encoded protein was also isolated and characterized as the cAMP-response element binding protein 2 (CREB-2). The protein encoded by this gene belongs to a family of DNA-binding proteins that includes the AP-1 family of transcription factors, cAMP-response element binding proteins (CREBs) and CREB-like proteins. These transcription factors share a leucine zipper region that is involved in protein-protein interactions, located C-terminal to a stretch of basic amino acids that functions as a DNA binding domain. Two alternative transcripts encoding the same protein have been described. Two pseudogenes are located on the X chromosome at q28 in a region containing a large inverted duplication. [provided by RefSeq, Sep 2011]","start":39519695,"end":39522685,"strand":1,"description":"activating transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:786]"}, {"versioned_ensembl_gene_id":"ENSG00000270808.1","gene_symbol":"AC022400.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73740538,"end":73740823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108592.16","gene_symbol":"FTSJ3","gene_name":"FtsJ homolog 3 [Source:HGNC Symbol;Acc:HGNC:17136]","synonyms":"SPB1","biotype":"protein_coding","ncbi_id":"117246","summary":"Although the function of this gene is not known, the existence of this gene is supported by mRNA and EST data. A possible function of the encoded protein can be inferred from amino acid sequence similarity to the E.coli FtsJ protein and to a mouse protein possibly involved in embryogenesis. [provided by RefSeq, Jul 2008]","start":63819433,"end":63830012,"strand":-1,"description":"FtsJ homolog 3 [Source:HGNC Symbol;Acc:HGNC:17136]"}, {"versioned_ensembl_gene_id":"ENSG00000271321.1","gene_symbol":"CTAGE6","gene_name":"CTAGE family member 6 [Source:HGNC Symbol;Acc:HGNC:28644]","synonyms":"MGC41943,CTAGE6P","biotype":"protein_coding","ncbi_id":"340307","summary":null,"start":143755089,"end":143757696,"strand":-1,"description":"CTAGE family member 6 [Source:HGNC Symbol;Acc:HGNC:28644]"}, {"versioned_ensembl_gene_id":"ENSG00000274270.1","gene_symbol":"AL137060.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50125816,"end":50128463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279162.1","gene_symbol":"AC141586.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2592514,"end":2594563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261140.1","gene_symbol":"AC093525.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2569043,"end":2571936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100567.12","gene_symbol":"PSMA3","gene_name":"proteasome subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:9532]","synonyms":"HC8","biotype":"protein_coding","ncbi_id":"5684","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Two alternative transcripts encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":58244831,"end":58272012,"strand":1,"description":"proteasome subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:9532]"}, {"versioned_ensembl_gene_id":"ENSG00000258682.1","gene_symbol":"AL132989.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":58264662,"end":58269681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260296.1","gene_symbol":"AC095057.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":40166675,"end":40167831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230941.1","gene_symbol":"AC002386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109322320,"end":109326315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279043.1","gene_symbol":"AC004014.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108900105,"end":108905226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232164.1","gene_symbol":"LINC01873","gene_name":"long intergenic non-protein coding RNA 1873 [Source:HGNC Symbol;Acc:HGNC:52692]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729348","summary":null,"start":66383306,"end":66392450,"strand":1,"description":"long intergenic non-protein coding RNA 1873 [Source:HGNC Symbol;Acc:HGNC:52692]"}, {"versioned_ensembl_gene_id":"ENSG00000243378.1","gene_symbol":"AC083801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182691928,"end":182692285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262681.2","gene_symbol":"AC005722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19719059,"end":19722428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131467.10","gene_symbol":"PSME3","gene_name":"proteasome activator subunit 3 [Source:HGNC Symbol;Acc:HGNC:9570]","synonyms":"REG-GAMMA,PA28G,PA28-gamma,Ki","biotype":"protein_coding","ncbi_id":"10197","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the gamma subunit of the 11S regulator. Six gamma subunits combine to form a homohexameric ring. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":42824385,"end":42843758,"strand":1,"description":"proteasome activator subunit 3 [Source:HGNC Symbol;Acc:HGNC:9570]"}, {"versioned_ensembl_gene_id":"ENSG00000274699.4","gene_symbol":"TAS2R30","gene_name":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]","synonyms":"TAS2R47,T2R30","biotype":"protein_coding","ncbi_id":"259293","summary":null,"start":11129613,"end":11130572,"strand":-1,"description":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]"}, {"versioned_ensembl_gene_id":"ENSG00000282256.1","gene_symbol":"TAS2R31","gene_name":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]","synonyms":"TAS2R44,T2R53,T2R31","biotype":"protein_coding","ncbi_id":"259290","summary":"TAS2R44 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11030686,"end":11031706,"strand":-1,"description":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]"}, {"versioned_ensembl_gene_id":"ENSG00000278111.4","gene_symbol":"TAS2R46","gene_name":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]","synonyms":"T2R54","biotype":"protein_coding","ncbi_id":"259292","summary":"TAS2R46 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Sep 2009]","start":11063523,"end":11064452,"strand":-1,"description":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]"}, {"versioned_ensembl_gene_id":"ENSG00000188227.12","gene_symbol":"ZNF793","gene_name":"zinc finger protein 793 [Source:HGNC Symbol;Acc:HGNC:33115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390927","summary":null,"start":37506939,"end":37548762,"strand":1,"description":"zinc finger protein 793 [Source:HGNC Symbol;Acc:HGNC:33115]"}, {"versioned_ensembl_gene_id":"ENSG00000283162.1","gene_symbol":"AL390726.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38433696,"end":38543880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205794.4","gene_symbol":"AC098591.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":40042917,"end":40057199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178752.15","gene_symbol":"ERFE","gene_name":"erythroferrone [Source:HGNC Symbol;Acc:HGNC:26727]","synonyms":"FLJ37034,FAM132B,CTRP15,C1QTNF15","biotype":"protein_coding","ncbi_id":"151176","summary":null,"start":238158982,"end":238168900,"strand":1,"description":"erythroferrone [Source:HGNC Symbol;Acc:HGNC:26727]"}, {"versioned_ensembl_gene_id":"ENSG00000270820.5","gene_symbol":"AC016727.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61471188,"end":61484130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243220.1","gene_symbol":"AC006159.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116563594,"end":116571234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254227.1","gene_symbol":"AC024681.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125998994,"end":126001001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268711.1","gene_symbol":"AC008750.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51426347,"end":51426668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258593.2","gene_symbol":"AL583810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104857792,"end":104858836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282014.1","gene_symbol":"TRBV4-1","gene_name":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]","synonyms":"TCRBV4S1,BV07S1J2.7,TRBV41,TCRBV7S1A1N2T","biotype":"TR_V_gene","ncbi_id":"28617","summary":null,"start":142313207,"end":142313689,"strand":1,"description":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]"}, {"versioned_ensembl_gene_id":"ENSG00000228589.3","gene_symbol":"SPCS2P4","gene_name":"signal peptidase complex subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45237]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653566","summary":null,"start":28095742,"end":28096422,"strand":-1,"description":"signal peptidase complex subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45237]"}, {"versioned_ensembl_gene_id":"ENSG00000234203.1","gene_symbol":"AC004771.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4972851,"end":4974681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224004.2","gene_symbol":"ATP5C1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:834]","synonyms":"ATP5CL2,ATP5C2","biotype":"processed_pseudogene","ncbi_id":"645560","summary":null,"start":53991101,"end":53991995,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:834]"}, {"versioned_ensembl_gene_id":"ENSG00000261970.1","gene_symbol":"AL391840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79552794,"end":79553160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186687.15","gene_symbol":"LYRM7","gene_name":"LYR motif containing 7 [Source:HGNC Symbol;Acc:HGNC:28072]","synonyms":"MZM1L,FLJ20796,C5orf31","biotype":"protein_coding","ncbi_id":"90624","summary":"Inner mitochondrial membrane complex III (CIII) is the main enzyme complex in the mitochondrial respiratory chain, and Rieske Fe-S protein (UQCRFS1) is the last catalytic subunit added to the complex. The protein encoded by this gene is a nuclear-encoded mitochondrial matrix protein that stabilizes UQCRFS1 and chaperones it to the CIII complex. Defects in this gene are a cause of mitochondrial complex III deficiency, nuclear type 8. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":131170810,"end":131205426,"strand":1,"description":"LYR motif containing 7 [Source:HGNC Symbol;Acc:HGNC:28072]"}, {"versioned_ensembl_gene_id":"ENSG00000228209.1","gene_symbol":"AC073091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76258034,"end":76258897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100335.13","gene_symbol":"MIEF1","gene_name":"mitochondrial elongation factor 1 [Source:HGNC Symbol;Acc:HGNC:25979]","synonyms":"SMCR7L,MiD51,FLJ20232","biotype":"protein_coding","ncbi_id":"54471","summary":null,"start":39499432,"end":39518132,"strand":1,"description":"mitochondrial elongation factor 1 [Source:HGNC Symbol;Acc:HGNC:25979]"}, {"versioned_ensembl_gene_id":"ENSG00000226950.6","gene_symbol":"DANCR","gene_name":"differentiation antagonizing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:28964]","synonyms":"SNHG13,lncRNA-ANCR,KIAA0114,ANCR,AGU2","biotype":"processed_transcript","ncbi_id":"57291","summary":"This gene produces a long non-coding RNA that functions as a negative regulator of cell differentiation. This transcript associates with enhancer of zeste homolog 2 to repress expression of the runt related transcription factor 2 gene. Increased expression of this transcript may be associated with cancer. Alternatively spliced transcript variants have been observed. [provided by RefSeq, Dec 2016]","start":52712404,"end":52720351,"strand":1,"description":"differentiation antagonizing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:28964]"}, {"versioned_ensembl_gene_id":"ENSG00000227157.1","gene_symbol":"AC068535.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104411201,"end":104415612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260165.1","gene_symbol":"AC105036.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75480661,"end":75480836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271816.1","gene_symbol":"BMS1P4","gene_name":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:NCBI gene;Acc:729096]","synonyms":"OTTHUMG00000018478,BMS1LP4,BMS1LP4","biotype":"processed_transcript","ncbi_id":"729096","summary":null,"start":73699151,"end":73730487,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:NCBI gene;Acc:729096]"}, {"versioned_ensembl_gene_id":"ENSG00000260235.1","gene_symbol":"AC105020.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75624793,"end":75625690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237801.6","gene_symbol":"AMD1P2","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:460]","synonyms":"AMDPY,AMDPX,AMDP1,AMD2,AMD","biotype":"processed_pseudogene","ncbi_id":"263","summary":null,"start":155828585,"end":155829576,"strand":-1,"description":"adenosylmethionine decarboxylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:460]"}, {"versioned_ensembl_gene_id":"ENSG00000213304.3","gene_symbol":"AC008481.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11521968,"end":11522498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217483.1","gene_symbol":"FO393414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72522641,"end":72523238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235226.1","gene_symbol":"AL445528.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159759170,"end":159759589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228836.8","gene_symbol":"CT45A5","gene_name":"cancer/testis antigen family 45 member A5 [Source:HGNC Symbol;Acc:HGNC:33270]","synonyms":"CT45.5,CT45-5","biotype":"protein_coding","ncbi_id":"441521","summary":"This gene represents one of a cluster of several similar genes located on the q arm of chromosome X. The genes in this cluster encode members of the cancer/testis (CT) family of antigens, and are distinct from other CT antigens. These antigens are thought to be novel therapeutic targets for human cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":135777130,"end":135785298,"strand":-1,"description":"cancer/testis antigen family 45 member A5 [Source:HGNC Symbol;Acc:HGNC:33270]"}, {"versioned_ensembl_gene_id":"ENSG00000274312.1","gene_symbol":"AC015722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98319687,"end":98320237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240069.1","gene_symbol":"GPAA1P1","gene_name":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4447]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"22945","summary":null,"start":109984058,"end":109984988,"strand":1,"description":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4447]"}, {"versioned_ensembl_gene_id":"ENSG00000250568.1","gene_symbol":"AC098591.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39973128,"end":39973442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226532.1","gene_symbol":"AL022718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124326175,"end":124326258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272347.1","gene_symbol":"AC116351.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1005039,"end":1006623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254541.1","gene_symbol":"AC023078.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18886933,"end":18887920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179776.17","gene_symbol":"CDH5","gene_name":"cadherin 5 [Source:HGNC Symbol;Acc:HGNC:1764]","synonyms":"CD144,7B4","biotype":"protein_coding","ncbi_id":"1003","summary":"This gene encodes a classical cadherin of the cadherin superfamily. The encoded preproprotein is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion molecule is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Functioning as a classical cadherin by imparting to cells the ability to adhere in a homophilic manner, this protein plays a role in endothelial adherens junction assembly and maintenance. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. [provided by RefSeq, Nov 2015]","start":66366622,"end":66404786,"strand":1,"description":"cadherin 5 [Source:HGNC Symbol;Acc:HGNC:1764]"}, {"versioned_ensembl_gene_id":"ENSG00000149531.15","gene_symbol":"FRG1BP","gene_name":"FSHD region gene 1 family member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:15792]","synonyms":"FRG1B,C20orf80,bA348I14.2","biotype":"unprocessed_pseudogene","ncbi_id":"284802","summary":null,"start":30377372,"end":30399257,"strand":1,"description":"FSHD region gene 1 family member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:15792]"}, {"versioned_ensembl_gene_id":"ENSG00000230598.2","gene_symbol":"AL645937.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29212886,"end":29216933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162378.12","gene_symbol":"ZYG11B","gene_name":"zyg-11 family member B, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:25820]","synonyms":"ZYG11,FLJ13456","biotype":"protein_coding","ncbi_id":"79699","summary":null,"start":52726467,"end":52827342,"strand":1,"description":"zyg-11 family member B, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:25820]"}, {"versioned_ensembl_gene_id":"ENSG00000223711.1","gene_symbol":"AC069213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":195544048,"end":195550581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284614.1","gene_symbol":"AF228730.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7221713,"end":7221930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251345.2","gene_symbol":"AC093826.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129133106,"end":129134098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213604.4","gene_symbol":"AC022882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56205125,"end":56205625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280117.1","gene_symbol":"AC122688.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125160525,"end":125164918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282423.1","gene_symbol":"TRBV1","gene_name":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]","synonyms":"TCRBV27S1P,TCRBV1S1P","biotype":"TR_V_pseudogene","ncbi_id":"28621","summary":null,"start":142299217,"end":142299500,"strand":1,"description":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]"}, {"versioned_ensembl_gene_id":"ENSG00000228968.1","gene_symbol":"AC096554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104125268,"end":104147229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232307.1","gene_symbol":"DAOA-AS1","gene_name":"DAOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30243]","synonyms":"G30,DAOAAS,DAOA-AS","biotype":"antisense_RNA","ncbi_id":"282706","summary":null,"start":105459055,"end":105505681,"strand":-1,"description":"DAOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30243]"}, {"versioned_ensembl_gene_id":"ENSG00000225792.1","gene_symbol":"AC004540.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26372144,"end":26376701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145041.15","gene_symbol":"DCAF1","gene_name":"DDB1 and CUL4 associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30911]","synonyms":"VPRBP,MGC102804,KIAA0800","biotype":"protein_coding","ncbi_id":"9730","summary":null,"start":51395867,"end":51500002,"strand":-1,"description":"DDB1 and CUL4 associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30911]"}, {"versioned_ensembl_gene_id":"ENSG00000081248.10","gene_symbol":"CACNA1S","gene_name":"calcium voltage-gated channel subunit alpha1 S [Source:HGNC Symbol;Acc:HGNC:1397]","synonyms":"MHS5,hypoPP,HOKPP,Cav1.1,CACNL1A3","biotype":"protein_coding","ncbi_id":"779","summary":"This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility. [provided by RefSeq, Jul 2008]","start":201039512,"end":201112566,"strand":-1,"description":"calcium voltage-gated channel subunit alpha1 S [Source:HGNC Symbol;Acc:HGNC:1397]"}, {"versioned_ensembl_gene_id":"ENSG00000232469.1","gene_symbol":"CR753509.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29290747,"end":29291689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231930.1","gene_symbol":"AF228730.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7200756,"end":7200857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214268.2","gene_symbol":"AF228730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7190901,"end":7191563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229347.1","gene_symbol":"AL596268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35058927,"end":35059974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259167.2","gene_symbol":"NMNAT1P1","gene_name":"NMNAT1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20024]","synonyms":"NMNATP","biotype":"processed_pseudogene","ncbi_id":"326607","summary":null,"start":81032529,"end":81033404,"strand":1,"description":"NMNAT1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20024]"}, {"versioned_ensembl_gene_id":"ENSG00000233861.1","gene_symbol":"MGAT2P1","gene_name":"MGAT2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51244]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422588","summary":null,"start":135730733,"end":135732197,"strand":-1,"description":"MGAT2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51244]"}, {"versioned_ensembl_gene_id":"ENSG00000097046.12","gene_symbol":"CDC7","gene_name":"cell division cycle 7 [Source:HGNC Symbol;Acc:HGNC:1745]","synonyms":"huCdc7,Hsk1,HsCdc7,CDC7L1","biotype":"protein_coding","ncbi_id":"8317","summary":"This gene encodes a cell division cycle protein with kinase activity that is critical for the G1/S transition. The yeast homolog is also essential for initiation of DNA replication as cell division occurs. Overexpression of this gene product may be associated with neoplastic transformation for some tumors. Multiple alternatively spliced transcript variants that encode the same protein have been detected. [provided by RefSeq, Aug 2008]","start":91500893,"end":91525764,"strand":1,"description":"cell division cycle 7 [Source:HGNC Symbol;Acc:HGNC:1745]"}, {"versioned_ensembl_gene_id":"ENSG00000229892.1","gene_symbol":"AL035666.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42606694,"end":42607559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263343.1","gene_symbol":"AC009088.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31165648,"end":31165927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273704.1","gene_symbol":"AL596245.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34768327,"end":34768688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231138.1","gene_symbol":"AC009987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123776670,"end":123777749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234351.1","gene_symbol":"CR753509.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29268481,"end":29269440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260902.1","gene_symbol":"LINC02011","gene_name":"long intergenic non-protein coding RNA 2011 [Source:HGNC Symbol;Acc:HGNC:27191]","synonyms":"FLJ31836","biotype":"lincRNA","ncbi_id":"152274","summary":null,"start":14799331,"end":14811414,"strand":-1,"description":"long intergenic non-protein coding RNA 2011 [Source:HGNC Symbol;Acc:HGNC:27191]"}, {"versioned_ensembl_gene_id":"ENSG00000171105.13","gene_symbol":"INSR","gene_name":"insulin receptor [Source:HGNC Symbol;Acc:HGNC:6091]","synonyms":"CD220","biotype":"protein_coding","ncbi_id":"3643","summary":"This gene encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form a heterotetrameric receptor. Binding of insulin or other ligands to this receptor activates the insulin signaling pathway, which regulates glucose uptake and release, as well as the synthesis and storage of carbohydrates, lipids and protein. Mutations in this gene underlie the inherited severe insulin resistance syndromes including type A insulin resistance syndrome, Donohue syndrome and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":7112255,"end":7294034,"strand":-1,"description":"insulin receptor [Source:HGNC Symbol;Acc:HGNC:6091]"}, {"versioned_ensembl_gene_id":"ENSG00000236880.1","gene_symbol":"Z85995.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124688504,"end":124688838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182346.18","gene_symbol":"DAOA","gene_name":"D-amino acid oxidase activator [Source:HGNC Symbol;Acc:HGNC:21191]","synonyms":"G72","biotype":"protein_coding","ncbi_id":"267012","summary":"This gene encodes a protein that may function as an activator of D-amino acid oxidase, which degrades the gliotransmitter D-serine, a potent activator of N-methyl-D-aspartate (NMDA) type glutamate receptors. Studies also suggest that one encoded isoform may play a role in mitochondrial function and dendritic arborization. Polymorphisms in this gene have been implicated in susceptibility to schizophrenia and bipolar affective disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Mar 2011]","start":105465867,"end":105491034,"strand":1,"description":"D-amino acid oxidase activator [Source:HGNC Symbol;Acc:HGNC:21191]"}, {"versioned_ensembl_gene_id":"ENSG00000257940.1","gene_symbol":"AC079598.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87816486,"end":87817831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227209.1","gene_symbol":"WARS2P1","gene_name":"tryptophanyl tRNA synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421633","summary":null,"start":80940665,"end":80941201,"strand":-1,"description":"tryptophanyl tRNA synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45116]"}, {"versioned_ensembl_gene_id":"ENSG00000099377.13","gene_symbol":"HSD3B7","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 [Source:HGNC Symbol;Acc:HGNC:18324]","synonyms":"SDR11E3,C(27)-3BETA-HSD","biotype":"protein_coding","ncbi_id":"80270","summary":"This gene encodes an enzyme which is involved in the initial stages of the synthesis of bile acids from cholesterol and a member of the short-chain dehydrogenase/reductase superfamily. The encoded protein is a membrane-associated endoplasmic reticulum protein which is active against 7-alpha hydrosylated sterol substrates. Mutations in this gene are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis, a form of progressive liver disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":30985207,"end":30989152,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 [Source:HGNC Symbol;Acc:HGNC:18324]"}, {"versioned_ensembl_gene_id":"ENSG00000169087.10","gene_symbol":"HSPBAP1","gene_name":"HSPB1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16389]","synonyms":"PASS1,FLJ22623","biotype":"protein_coding","ncbi_id":"79663","summary":"This gene encodes a protein that binds to one of the small heat shock proteins, specifically hsp27. Hsp27 is involved with cell growth and differentiation. This encoded protein was found to be abnormally expressed in patients with intractable epilepsy, although how brain function is affected remains unknown. [provided by RefSeq, Sep 2011]","start":122740003,"end":122793824,"strand":-1,"description":"HSPB1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16389]"}, {"versioned_ensembl_gene_id":"ENSG00000268940.5","gene_symbol":"CT45A1","gene_name":"cancer/testis antigen family 45 member A1 [Source:HGNC Symbol;Acc:HGNC:33267]","synonyms":"CT45.1,CT45-1","biotype":"protein_coding","ncbi_id":"541466","summary":null,"start":135713453,"end":135723539,"strand":1,"description":"cancer/testis antigen family 45 member A1 [Source:HGNC Symbol;Acc:HGNC:33267]"}, {"versioned_ensembl_gene_id":"ENSG00000255217.1","gene_symbol":"AP003034.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56165500,"end":56165921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225823.1","gene_symbol":"RPL7P45","gene_name":"ribosomal protein L7 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35522]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271225","summary":null,"start":104814327,"end":104815069,"strand":1,"description":"ribosomal protein L7 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35522]"}, {"versioned_ensembl_gene_id":"ENSG00000223603.1","gene_symbol":"CRPP1","gene_name":"C-reactive protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2368]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"171422","summary":null,"start":159704983,"end":159705607,"strand":-1,"description":"C-reactive protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2368]"}, {"versioned_ensembl_gene_id":"ENSG00000198022.6","gene_symbol":"SAGE2P","gene_name":"sarcoma antigen 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:51337]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644717","summary":null,"start":135673591,"end":135686151,"strand":-1,"description":"sarcoma antigen 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:51337]"}, {"versioned_ensembl_gene_id":"ENSG00000181752.3","gene_symbol":"OR8K5","gene_name":"olfactory receptor family 8 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:15315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219453","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56159394,"end":56160317,"strand":-1,"description":"olfactory receptor family 8 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:15315]"}, {"versioned_ensembl_gene_id":"ENSG00000235257.8","gene_symbol":"ITGA9-AS1","gene_name":"ITGA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49668]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101928153","summary":null,"start":37745432,"end":37861780,"strand":-1,"description":"ITGA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49668]"}, {"versioned_ensembl_gene_id":"ENSG00000162377.5","gene_symbol":"COA7","gene_name":"cytochrome c oxidase assembly factor 7 (putative) [Source:HGNC Symbol;Acc:HGNC:25716]","synonyms":"SELRC1,RESA1,FLJ12439,C1orf163","biotype":"protein_coding","ncbi_id":"65260","summary":null,"start":52684451,"end":52698366,"strand":-1,"description":"cytochrome c oxidase assembly factor 7 (putative) [Source:HGNC Symbol;Acc:HGNC:25716]"}, {"versioned_ensembl_gene_id":"ENSG00000236411.1","gene_symbol":"NDUFAF4P3","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422532","summary":null,"start":37789921,"end":37790445,"strand":-1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44542]"}, {"versioned_ensembl_gene_id":"ENSG00000158731.2","gene_symbol":"OR10J6P","gene_name":"olfactory receptor family 10 subfamily J member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14994]","synonyms":"OR10J6","biotype":"unprocessed_pseudogene","ncbi_id":"401973","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159598298,"end":159599227,"strand":1,"description":"olfactory receptor family 10 subfamily J member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14994]"}, {"versioned_ensembl_gene_id":"ENSG00000230474.1","gene_symbol":"ATP6V1G1P7","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874514","summary":null,"start":103444620,"end":103444968,"strand":-1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39852]"}, {"versioned_ensembl_gene_id":"ENSG00000224978.1","gene_symbol":"BX682237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155212921,"end":155213638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132692.18","gene_symbol":"BCAN","gene_name":"brevican [Source:HGNC Symbol;Acc:HGNC:23059]","synonyms":"MGC13038,CSPG7,BEHAB","biotype":"protein_coding","ncbi_id":"63827","summary":"This gene encodes a member of the lectican family of chondroitin sulfate proteoglycans that is specifically expressed in the central nervous system. This protein is developmentally regulated and may function in the formation of the brain extracellular matrix. This protein is highly expressed in gliomas and may promote the growth and cell motility of brain tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":156641390,"end":156659532,"strand":1,"description":"brevican [Source:HGNC Symbol;Acc:HGNC:23059]"}, {"versioned_ensembl_gene_id":"ENSG00000282264.1","gene_symbol":"AC231381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142285779,"end":142288898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079931.14","gene_symbol":"MOXD1","gene_name":"monooxygenase DBH like 1 [Source:HGNC Symbol;Acc:HGNC:21063]","synonyms":"MOX,DKFZP564G202,dJ248E1.1","biotype":"protein_coding","ncbi_id":"26002","summary":null,"start":132296055,"end":132401545,"strand":-1,"description":"monooxygenase DBH like 1 [Source:HGNC Symbol;Acc:HGNC:21063]"}, {"versioned_ensembl_gene_id":"ENSG00000234551.1","gene_symbol":"LINC01309","gene_name":"long intergenic non-protein coding RNA 1309 [Source:HGNC Symbol;Acc:HGNC:50497]","synonyms":"TCONS_l2_00007459","biotype":"lincRNA","ncbi_id":"104326190","summary":null,"start":103425200,"end":103427685,"strand":1,"description":"long intergenic non-protein coding RNA 1309 [Source:HGNC Symbol;Acc:HGNC:50497]"}, {"versioned_ensembl_gene_id":"ENSG00000272405.1","gene_symbol":"AL365181.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156641666,"end":156644887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227286.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33020794,"end":33026336,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000236141.1","gene_symbol":"AC013727.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103865746,"end":103869688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155714.13","gene_symbol":"PDZD9","gene_name":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]","synonyms":"C16orf65,MGC50721","biotype":"protein_coding","ncbi_id":"255762","summary":null,"start":21983865,"end":22001110,"strand":-1,"description":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]"}, {"versioned_ensembl_gene_id":"ENSG00000227994.1","gene_symbol":"AL035417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44172506,"end":44172719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254863.1","gene_symbol":"AP001360.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119987954,"end":119995037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145050.15","gene_symbol":"MANF","gene_name":"mesencephalic astrocyte derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:15461]","synonyms":"ARP,ARMET","biotype":"protein_coding","ncbi_id":"7873","summary":"The protein encoded by this gene is localized in the endoplasmic reticulum (ER) and golgi, and is also secreted. Reducing expression of this gene increases susceptibility to ER stress-induced death and results in cell proliferation. Activity of this protein is important in promoting the survival of dopaminergic neurons. The presence of polymorphisms in the N-terminal arginine-rich region, including a specific mutation that changes an ATG start codon to AGG, have been reported in a variety of solid tumors; however, these polymorphisms were later shown to exist in normal tissues and are thus no longer thought to be tumor-related. [provided by RefSeq, Apr 2014]","start":51385047,"end":51389397,"strand":1,"description":"mesencephalic astrocyte derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:15461]"}, {"versioned_ensembl_gene_id":"ENSG00000282303.1","gene_symbol":"PRSS3P3","gene_name":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]","synonyms":"TRY3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"136540","summary":null,"start":142287280,"end":142289809,"strand":-1,"description":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]"}, {"versioned_ensembl_gene_id":"ENSG00000256637.6","gene_symbol":"LINC01965","gene_name":"long intergenic non-protein coding RNA 1965 [Source:HGNC Symbol;Acc:HGNC:52790]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985928","summary":null,"start":103874310,"end":104077778,"strand":1,"description":"long intergenic non-protein coding RNA 1965 [Source:HGNC Symbol;Acc:HGNC:52790]"}, {"versioned_ensembl_gene_id":"ENSG00000121898.12","gene_symbol":"CPXM2","gene_name":"carboxypeptidase X, M14 family member 2 [Source:HGNC Symbol;Acc:HGNC:26977]","synonyms":"UNQ676,CPX2","biotype":"protein_coding","ncbi_id":"119587","summary":null,"start":123706207,"end":123940267,"strand":-1,"description":"carboxypeptidase X, M14 family member 2 [Source:HGNC Symbol;Acc:HGNC:26977]"}, {"versioned_ensembl_gene_id":"ENSG00000234677.1","gene_symbol":"AC068058.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123913574,"end":123931597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110492.15","gene_symbol":"MDK","gene_name":"midkine (neurite growth-promoting factor 2) [Source:HGNC Symbol;Acc:HGNC:6972]","synonyms":"NEGF2,MK,FLJ27379","biotype":"protein_coding","ncbi_id":"4192","summary":"This gene encodes a member of a small family of secreted growth factors that binds heparin and responds to retinoic acid. The encoded protein promotes cell growth, migration, and angiogenesis, in particular during tumorigenesis. This gene has been targeted as a therapeutic for a variety of different disorders. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012]","start":46380756,"end":46383837,"strand":1,"description":"midkine (neurite growth-promoting factor 2) [Source:HGNC Symbol;Acc:HGNC:6972]"}, {"versioned_ensembl_gene_id":"ENSG00000261634.3","gene_symbol":"AC026992.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69278328,"end":69298763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259074.1","gene_symbol":"PSMB7P1","gene_name":"PSMB7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49192]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422289","summary":null,"start":20149232,"end":20149745,"strand":1,"description":"PSMB7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49192]"}, {"versioned_ensembl_gene_id":"ENSG00000225733.5","gene_symbol":"FGD5-AS1","gene_name":"FGD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40410]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505641","summary":null,"start":14920347,"end":14948424,"strand":-1,"description":"FGD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40410]"}, {"versioned_ensembl_gene_id":"ENSG00000189325.6","gene_symbol":"C6orf222","gene_name":"chromosome 6 open reading frame 222 [Source:HGNC Symbol;Acc:HGNC:33769]","synonyms":"DKFZp779B1540","biotype":"protein_coding","ncbi_id":"389384","summary":null,"start":36315757,"end":36336885,"strand":-1,"description":"chromosome 6 open reading frame 222 [Source:HGNC Symbol;Acc:HGNC:33769]"}, {"versioned_ensembl_gene_id":"ENSG00000259504.2","gene_symbol":"AC026992.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69278675,"end":69295322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165752.16","gene_symbol":"STK32C","gene_name":"serine/threonine kinase 32C [Source:HGNC Symbol;Acc:HGNC:21332]","synonyms":"YANK3,PKE,MGC23665","biotype":"protein_coding","ncbi_id":"282974","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. It is thought that this family member is functional in brain due to its high expression levels there. DNA methylation differences have been found in this gene in monozygotic twins that are discordant for adolescent depression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":132207492,"end":132331847,"strand":-1,"description":"serine/threonine kinase 32C [Source:HGNC Symbol;Acc:HGNC:21332]"}, {"versioned_ensembl_gene_id":"ENSG00000266899.2","gene_symbol":"AKR1B1P7","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33497]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126242","summary":null,"start":33360497,"end":33361448,"strand":-1,"description":"aldo-keto reductase family 1 member B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33497]"}, {"versioned_ensembl_gene_id":"ENSG00000277486.1","gene_symbol":"SAGE3P","gene_name":"sarcoma antigen 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:51338]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419054","summary":null,"start":135637623,"end":135642756,"strand":-1,"description":"sarcoma antigen 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:51338]"}, {"versioned_ensembl_gene_id":"ENSG00000215802.3","gene_symbol":"RFKP1","gene_name":"riboflavin kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39181]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100313962","summary":null,"start":240823006,"end":240823433,"strand":-1,"description":"riboflavin kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39181]"}, {"versioned_ensembl_gene_id":"ENSG00000139637.13","gene_symbol":"C12orf10","gene_name":"chromosome 12 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:17590]","synonyms":"MYG1,MYG,Gamm1","biotype":"protein_coding","ncbi_id":"60314","summary":null,"start":53299686,"end":53307177,"strand":1,"description":"chromosome 12 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:17590]"}, {"versioned_ensembl_gene_id":"ENSG00000238085.1","gene_symbol":"AL590682.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240998451,"end":240998794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233615.1","gene_symbol":"HNRNPA1P42","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48771]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287266","summary":null,"start":240919653,"end":240920609,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48771]"}, {"versioned_ensembl_gene_id":"ENSG00000235589.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994750,"end":29005281,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000243864.1","gene_symbol":"RPS3AP50","gene_name":"ribosomal protein S3a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:37018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271601","summary":null,"start":33340686,"end":33341984,"strand":1,"description":"ribosomal protein S3a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:37018]"}, {"versioned_ensembl_gene_id":"ENSG00000267130.1","gene_symbol":"AC008738.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33305036,"end":33309387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159377.10","gene_symbol":"PSMB4","gene_name":"proteasome subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:9541]","synonyms":"PROS26,HN3","biotype":"protein_coding","ncbi_id":"5692","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. [provided by RefSeq, Jul 2008]","start":151399534,"end":151401944,"strand":1,"description":"proteasome subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:9541]"}, {"versioned_ensembl_gene_id":"ENSG00000177791.11","gene_symbol":"MYOZ1","gene_name":"myozenin 1 [Source:HGNC Symbol;Acc:HGNC:13752]","synonyms":"MYOZ,FATZ,CS-2","biotype":"protein_coding","ncbi_id":"58529","summary":"The protein encoded by this gene is primarily expressed in the skeletal muscle, and belongs to the myozenin family. Members of this family function as calcineurin-interacting proteins that help tether calcineurin to the sarcomere of cardiac and skeletal muscle. They play an important role in modulation of calcineurin signaling. [provided by RefSeq, Apr 2012]","start":73631654,"end":73641757,"strand":-1,"description":"myozenin 1 [Source:HGNC Symbol;Acc:HGNC:13752]"}, {"versioned_ensembl_gene_id":"ENSG00000254633.1","gene_symbol":"AL512590.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":97276566,"end":97295759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228495.1","gene_symbol":"LINC01013","gene_name":"long intergenic non-protein coding RNA 1013 [Source:HGNC Symbol;Acc:HGNC:48987]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507254","summary":null,"start":132131915,"end":132169374,"strand":1,"description":"long intergenic non-protein coding RNA 1013 [Source:HGNC Symbol;Acc:HGNC:48987]"}, {"versioned_ensembl_gene_id":"ENSG00000147485.12","gene_symbol":"PXDNL","gene_name":"peroxidasin like [Source:HGNC Symbol;Acc:HGNC:26359]","synonyms":"PMR1,FLJ25471","biotype":"protein_coding","ncbi_id":"137902","summary":null,"start":51319578,"end":51809445,"strand":-1,"description":"peroxidasin like [Source:HGNC Symbol;Acc:HGNC:26359]"}, {"versioned_ensembl_gene_id":"ENSG00000254848.1","gene_symbol":"OR5BN1P","gene_name":"olfactory receptor family 5 subfamily BN member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15276]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81204","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56132666,"end":56133494,"strand":-1,"description":"olfactory receptor family 5 subfamily BN member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15276]"}, {"versioned_ensembl_gene_id":"ENSG00000206281.11","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33228522,"end":33243221,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000256977.12","gene_symbol":"LIMS3","gene_name":"LIM zinc finger domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30047]","synonyms":null,"biotype":"protein_coding","ncbi_id":"96626","summary":null,"start":109898428,"end":109924868,"strand":1,"description":"LIM zinc finger domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30047]"}, {"versioned_ensembl_gene_id":"ENSG00000255040.1","gene_symbol":"MORF4L1P3","gene_name":"mortality factor 4 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20402]","synonyms":"MRG11,MORF4LP3","biotype":"processed_pseudogene","ncbi_id":"326593","summary":null,"start":14673606,"end":14674555,"strand":-1,"description":"mortality factor 4 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20402]"}, {"versioned_ensembl_gene_id":"ENSG00000235494.1","gene_symbol":"AL590705.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97233201,"end":97235014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260394.2","gene_symbol":"Z92544.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":678504,"end":679777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185219.16","gene_symbol":"ZNF445","gene_name":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]","synonyms":"ZSCAN47,ZNF168,ZKSCAN15","biotype":"protein_coding","ncbi_id":"353274","summary":null,"start":44431720,"end":44477670,"strand":-1,"description":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]"}, {"versioned_ensembl_gene_id":"ENSG00000109534.16","gene_symbol":"GAR1","gene_name":"GAR1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14264]","synonyms":"NOLA1","biotype":"protein_coding","ncbi_id":"54433","summary":"This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA2 and NOLA3 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. These four H/ACA snoRNP proteins are also components of the telomerase complex. The encoded protein of this gene contains two glycine- and arginine-rich domains and is related to Saccharomyces cerevisiae Gar1p. Two splice variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":109815510,"end":109824740,"strand":1,"description":"GAR1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14264]"}, {"versioned_ensembl_gene_id":"ENSG00000225873.3","gene_symbol":"LINC00694","gene_name":"long intergenic non-protein coding RNA 694 [Source:HGNC Symbol;Acc:HGNC:44570]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724231","summary":null,"start":44421127,"end":44439946,"strand":-1,"description":"long intergenic non-protein coding RNA 694 [Source:HGNC Symbol;Acc:HGNC:44570]"}, {"versioned_ensembl_gene_id":"ENSG00000167513.8","gene_symbol":"CDT1","gene_name":"chromatin licensing and DNA replication factor 1 [Source:HGNC Symbol;Acc:HGNC:24576]","synonyms":"RIS2,DUP","biotype":"protein_coding","ncbi_id":"81620","summary":"The protein encoded by this gene is involved in the formation of the pre-replication complex that is necessary for DNA replication. The encoded protein can bind geminin, which prevents replication and may function to prevent this protein from initiating replication at inappropriate origins. Phosphorylation of this protein by cyclin A-dependent kinases results in degradation of the protein. [provided by RefSeq, Mar 2011]","start":88803213,"end":88809258,"strand":1,"description":"chromatin licensing and DNA replication factor 1 [Source:HGNC Symbol;Acc:HGNC:24576]"}, {"versioned_ensembl_gene_id":"ENSG00000178150.9","gene_symbol":"ZNF114","gene_name":"zinc finger protein 114 [Source:HGNC Symbol;Acc:HGNC:12894]","synonyms":"MGC17986","biotype":"protein_coding","ncbi_id":"163071","summary":null,"start":48270102,"end":48287608,"strand":1,"description":"zinc finger protein 114 [Source:HGNC Symbol;Acc:HGNC:12894]"}, {"versioned_ensembl_gene_id":"ENSG00000229189.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31601313,"end":31601586,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000268186.1","gene_symbol":"AC008392.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48262900,"end":48271283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237426.1","gene_symbol":"ZIK1P1","gene_name":"zinc finger protein interacting with K protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38031]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131493","summary":null,"start":124173001,"end":124174459,"strand":-1,"description":"zinc finger protein interacting with K protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38031]"}, {"versioned_ensembl_gene_id":"ENSG00000280155.1","gene_symbol":"AL021408.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132130252,"end":132131795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267580.1","gene_symbol":"AC008738.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33299934,"end":33301168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176349.11","gene_symbol":"AC104129.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1838586,"end":1849931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102243.12","gene_symbol":"VGLL1","gene_name":"vestigial like family member 1 [Source:HGNC Symbol;Acc:HGNC:20985]","synonyms":"TONDU,TDU","biotype":"protein_coding","ncbi_id":"51442","summary":"The protein encoded by this gene binds proteins of the TEA domain family of transcription factors (TEFs) through the Vg (vestigial) homology region found in its N-terminus. It may thus function as a specific coactivator for the mammalian TEFs. [provided by RefSeq, Sep 2009]","start":136532152,"end":136556807,"strand":1,"description":"vestigial like family member 1 [Source:HGNC Symbol;Acc:HGNC:20985]"}, {"versioned_ensembl_gene_id":"ENSG00000245848.2","gene_symbol":"CEBPA","gene_name":"CCAAT/enhancer binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1833]","synonyms":"CEBP,C/EBP-alpha","biotype":"protein_coding","ncbi_id":"1050","summary":"This intronless gene encodes a transcription factor that contains a basic leucine zipper (bZIP) domain and recognizes the CCAAT motif in the promoters of target genes. The encoded protein functions in homodimers and also heterodimers with CCAAT/enhancer-binding proteins beta and gamma. Activity of this protein can modulate the expression of genes involved in cell cycle regulation as well as in body weight homeostasis. Mutation of this gene is associated with acute myeloid leukemia. The use of alternative in-frame non-AUG (GUG) and AUG start codons results in protein isoforms with different lengths. Differential translation initiation is mediated by an out-of-frame, upstream open reading frame which is located between the GUG and the first AUG start codons. [provided by RefSeq, Dec 2013]","start":33299934,"end":33302564,"strand":-1,"description":"CCAAT/enhancer binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1833]"}, {"versioned_ensembl_gene_id":"ENSG00000237723.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33386065,"end":33386688,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000282393.1","gene_symbol":"AC016588.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":248551,"end":251571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211810.3","gene_symbol":"TRAV29DV5","gene_name":"T-cell receptor alpha variable 29/delta variable 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12127]","synonyms":"TRAV29/DV5","biotype":"TR_V_gene","ncbi_id":"28653","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22163238,"end":22163870,"strand":1,"description":"T-cell receptor alpha variable 29/delta variable 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12127]"}, {"versioned_ensembl_gene_id":"ENSG00000258128.2","gene_symbol":"AC079598.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":87782163,"end":87784568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272795.1","gene_symbol":"AC126283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109815047,"end":109815410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214558.4","gene_symbol":"AL365217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65302522,"end":65304957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254821.1","gene_symbol":"AL136309.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4135423,"end":4146053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243828.2","gene_symbol":"AL355357.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64728837,"end":64733837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110925.6","gene_symbol":"CSRNP2","gene_name":"cysteine and serine rich nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16006]","synonyms":"TAIP-12,PPP1R72,FAM130A1,C12orf22,C12ORF2","biotype":"protein_coding","ncbi_id":"81566","summary":"The protein encoded by this gene belongs to the CSRNP family of nuclear proteins that share conserved regions, including cysteine- and serine- rich regions, a basic domain, a transcriptional activation domain, and bind the sequence 'AGAGTG', thus have the hallmark of transcription factors. Studies in mice suggest that these genes may have redundant functions. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":51061205,"end":51083664,"strand":-1,"description":"cysteine and serine rich nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16006]"}, {"versioned_ensembl_gene_id":"ENSG00000231115.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33378855,"end":33383082,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000241103.1","gene_symbol":"AC109925.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94369833,"end":94370163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154783.11","gene_symbol":"FGD5","gene_name":"FYVE, RhoGEF and PH domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19117]","synonyms":"ZFYVE23,FLJ39957,FLJ00274","biotype":"protein_coding","ncbi_id":"152273","summary":null,"start":14810853,"end":14934565,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19117]"}, {"versioned_ensembl_gene_id":"ENSG00000283175.1","gene_symbol":"AC007920.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":187291272,"end":187297933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166396.12","gene_symbol":"SERPINB7","gene_name":"serpin family B member 7 [Source:HGNC Symbol;Acc:HGNC:13902]","synonyms":"MEGSIN","biotype":"protein_coding","ncbi_id":"8710","summary":"This gene encodes a member of a family of proteins which function as protease inhibitors. Expression of this gene is upregulated in IgA nephropathy and mutations have been found to cause palmoplantar keratoderma, Nagashima type. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":63752935,"end":63805376,"strand":1,"description":"serpin family B member 7 [Source:HGNC Symbol;Acc:HGNC:13902]"}, {"versioned_ensembl_gene_id":"ENSG00000085224.21","gene_symbol":"ATRX","gene_name":"ATRX, chromatin remodeler [Source:HGNC Symbol;Acc:HGNC:886]","synonyms":"XNP,XH2,RAD54,MRX52,JMS","biotype":"protein_coding","ncbi_id":"546","summary":"The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with X-linked syndromes exhibiting cognitive disabilities as well as alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2017]","start":77504878,"end":77786269,"strand":-1,"description":"ATRX, chromatin remodeler [Source:HGNC Symbol;Acc:HGNC:886]"}, {"versioned_ensembl_gene_id":"ENSG00000184394.2","gene_symbol":"OR4N5","gene_name":"olfactory receptor family 4 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15358]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390437","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20138820,"end":20145471,"strand":1,"description":"olfactory receptor family 4 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15358]"}, {"versioned_ensembl_gene_id":"ENSG00000176246.1","gene_symbol":"OR4L1","gene_name":"olfactory receptor family 4 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:15356]","synonyms":"OR4L2P","biotype":"protein_coding","ncbi_id":"122742","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20060045,"end":20060983,"strand":1,"description":"olfactory receptor family 4 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:15356]"}, {"versioned_ensembl_gene_id":"ENSG00000167280.16","gene_symbol":"ENGASE","gene_name":"endo-beta-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:24622]","synonyms":"FLJ21865","biotype":"protein_coding","ncbi_id":"64772","summary":"This gene encodes a cytosolic enzyme which catalyzes the hydrolysis of peptides and proteins with mannose modifications to produce free oligosaccharides. [provided by RefSeq, Feb 2012]","start":79074939,"end":79088599,"strand":1,"description":"endo-beta-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:24622]"}, {"versioned_ensembl_gene_id":"ENSG00000163106.10","gene_symbol":"HPGDS","gene_name":"hematopoietic prostaglandin D synthase [Source:HGNC Symbol;Acc:HGNC:17890]","synonyms":"PGDS,PGD2,H-PGDS,GSTS1-1,GSTS1,GSTS","biotype":"protein_coding","ncbi_id":"27306","summary":"Prostaglandin-D synthase is a sigma class glutathione-S-transferase family member. The enzyme catalyzes the conversion of PGH2 to PGD2 and plays a role in the production of prostanoids in the immune system and mast cells. The presence of this enzyme can be used to identify the differentiation stage of human megakaryocytes. [provided by RefSeq, Jul 2008]","start":94298535,"end":94342876,"strand":-1,"description":"hematopoietic prostaglandin D synthase [Source:HGNC Symbol;Acc:HGNC:17890]"}, {"versioned_ensembl_gene_id":"ENSG00000249531.2","gene_symbol":"AC098799.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68300325,"end":68302459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241484.9","gene_symbol":"ARHGAP8","gene_name":"Rho GTPase activating protein 8 [Source:HGNC Symbol;Acc:HGNC:677]","synonyms":"FLJ20185,BPGAP1","biotype":"protein_coding","ncbi_id":"23779","summary":"This gene encodes a member of the RHOGAP family. GAP (GTPase-activating) family proteins participate in signaling pathways that regulate cell processes involved in cytoskeletal changes. GAP proteins alternate between an active (GTP-bound) and inactive (GDP-bound) state based on the GTP:GDP ratio in the cell. This family member is a multidomain protein that functions to promote Erk activation and cell motility. Alternative splicing results in multiple transcript variants. Read-through transcripts from the upstream proline rich 5, renal (PRR5) gene into this gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010]","start":44752558,"end":44862788,"strand":1,"description":"Rho GTPase activating protein 8 [Source:HGNC Symbol;Acc:HGNC:677]"}, {"versioned_ensembl_gene_id":"ENSG00000224348.2","gene_symbol":"AL592076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":241305580,"end":241305882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140090.17","gene_symbol":"SLC24A4","gene_name":"solute carrier family 24 member 4 [Source:HGNC Symbol;Acc:HGNC:10978]","synonyms":"NCKX4","biotype":"protein_coding","ncbi_id":"123041","summary":"This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]","start":92322581,"end":92501483,"strand":1,"description":"solute carrier family 24 member 4 [Source:HGNC Symbol;Acc:HGNC:10978]"}, {"versioned_ensembl_gene_id":"ENSG00000250642.3","gene_symbol":"AC098799.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68282461,"end":68285959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112130.16","gene_symbol":"RNF8","gene_name":"ring finger protein 8 [Source:HGNC Symbol;Acc:HGNC:10071]","synonyms":"KIAA0646","biotype":"protein_coding","ncbi_id":"9025","summary":"The protein encoded by this gene contains a RING finger motif and an FHA domain. This protein has been shown to interact with several class II ubiquitin-conjugating enzymes (E2), including UBE2E1/UBCH6, UBE2E2, and UBE2E3, and may act as an ubiquitin ligase (E3) in the ubiquitination of certain nuclear proteins. This protein is also known to play a role in the DNA damage response and depletion of this protein causes cell growth inhibition and cell cycle arrest. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":37353972,"end":37394738,"strand":1,"description":"ring finger protein 8 [Source:HGNC Symbol;Acc:HGNC:10071]"}, {"versioned_ensembl_gene_id":"ENSG00000235545.1","gene_symbol":"AC103923.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62688482,"end":62710694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232357.2","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"KE6,FABGL,SDR30C1,HKE6,D6S2245E,RING2,H2-KE6","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33375002,"end":33377191,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000166226.12","gene_symbol":"CCT2","gene_name":"chaperonin containing TCP1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:1615]","synonyms":"Cctb","biotype":"protein_coding","ncbi_id":"10576","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":69585334,"end":69601570,"strand":1,"description":"chaperonin containing TCP1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:1615]"}, {"versioned_ensembl_gene_id":"ENSG00000137875.4","gene_symbol":"BCL2L10","gene_name":"BCL2 like 10 [Source:HGNC Symbol;Acc:HGNC:993]","synonyms":"Diva,Boo,BCL-B","biotype":"protein_coding","ncbi_id":"10017","summary":"The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The protein encoded by this gene contains conserved BH4, BH1 and BH2 domains. This protein can interact with other members of BCL-2 protein family including BCL2, BCL2L1/BCL-X(L), and BAX. Overexpression of this gene has been shown to suppress cell apoptosis possibly through the prevention of cytochrome C release from the mitochondria, and thus activating caspase-3 activation. The mouse counterpart of this protein is found to interact with Apaf1 and forms a protein complex with Caspase 9, which suggests the involvement of this protein in APAF1 and CASPASE 9 related apoptotic pathway. [provided by RefSeq, Jul 2008]","start":52109263,"end":52112775,"strand":-1,"description":"BCL2 like 10 [Source:HGNC Symbol;Acc:HGNC:993]"}, {"versioned_ensembl_gene_id":"ENSG00000253395.1","gene_symbol":"AP003469.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101122145,"end":101126158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253664.1","gene_symbol":"AC012413.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51257688,"end":51321118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166860.2","gene_symbol":"ZBTB39","gene_name":"zinc finger and BTB domain containing 39 [Source:HGNC Symbol;Acc:HGNC:29014]","synonyms":"ZNF922,KIAA0352","biotype":"protein_coding","ncbi_id":"9880","summary":null,"start":56998834,"end":57006446,"strand":-1,"description":"zinc finger and BTB domain containing 39 [Source:HGNC Symbol;Acc:HGNC:29014]"}, {"versioned_ensembl_gene_id":"ENSG00000142512.14","gene_symbol":"SIGLEC10","gene_name":"sialic acid binding Ig like lectin 10 [Source:HGNC Symbol;Acc:HGNC:15620]","synonyms":"SLG2,SIGLEC-10,PRO940,MGC126774","biotype":"protein_coding","ncbi_id":"89790","summary":"SIGLECs are members of the immunoglobulin superfamily that are expressed on the cell surface. Most SIGLECs have 1 or more cytoplasmic immune receptor tyrosine-based inhibitory motifs, or ITIMs. SIGLECs are typically expressed on cells of the innate immune system, with the exception of the B-cell expressed SIGLEC6 (MIM 604405).[supplied by OMIM, Jul 2002]","start":51410021,"end":51417803,"strand":-1,"description":"sialic acid binding Ig like lectin 10 [Source:HGNC Symbol;Acc:HGNC:15620]"}, {"versioned_ensembl_gene_id":"ENSG00000279179.1","gene_symbol":"AL662907.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33162851,"end":33166298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230522.5","gene_symbol":"MBD3L2","gene_name":"methyl-CpG binding domain protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:18532]","synonyms":null,"biotype":"protein_coding","ncbi_id":"125997","summary":"This gene encodes a protein that is related to methyl-CpG-binding proteins but lacks the methyl-CpG binding domain. The protein has been found in germ cell tumors and some somatic tissues. [provided by RefSeq, Jul 2008]","start":7049321,"end":7051735,"strand":1,"description":"methyl-CpG binding domain protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:18532]"}, {"versioned_ensembl_gene_id":"ENSG00000234079.2","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31191499,"end":31197704,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000228469.1","gene_symbol":"CR388229.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31193904,"end":31195656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282053.1","gene_symbol":"AC019257.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1972570,"end":1974637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125629.14","gene_symbol":"INSIG2","gene_name":"insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51141","summary":"The protein encoded by this gene is highly similar to the protein product encoded by gene INSIG1. Both INSIG1 protein and this protein are endoplasmic reticulum proteins that block the processing of sterol regulatory element binding proteins (SREBPs) by binding to SREBP cleavage-activating protein (SCAP), and thus prevent SCAP from escorting SREBPs to the Golgi. [provided by RefSeq, Jul 2008]","start":118088452,"end":118110997,"strand":1,"description":"insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]"}, {"versioned_ensembl_gene_id":"ENSG00000228962.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"antisense_RNA","ncbi_id":"414764","summary":null,"start":32390510,"end":32393686,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000272791.1","gene_symbol":"AC073389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73630556,"end":73631490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232346.1","gene_symbol":"Z74021.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32039490,"end":32039896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228321.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31615015,"end":31617784,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000229209.1","gene_symbol":"AC073987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103109759,"end":103176260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253340.1","gene_symbol":"AC087272.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50859530,"end":50860062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269761.1","gene_symbol":"AC025278.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7005012,"end":7006074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226462.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969099,"end":28970429,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000278495.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769810,"end":54784323,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000242375.1","gene_symbol":"AL590705.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97195351,"end":97197687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204290.10","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32393963,"end":32407128,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000255160.5","gene_symbol":"AC009652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19299883,"end":19308358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254483.1","gene_symbol":"AL590705.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97238645,"end":97246184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227623.1","gene_symbol":"AC010881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103275904,"end":103276138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137757.10","gene_symbol":"CASP5","gene_name":"caspase 5 [Source:HGNC Symbol;Acc:HGNC:1506]","synonyms":"ICE(rel)III","biotype":"protein_coding","ncbi_id":"838","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. Overexpression of the active form of this enzyme induces apoptosis in fibroblasts. Max, a central component of the Myc/Max/Mad transcription regulation network important for cell growth, differentiation, and apoptosis, is cleaved by this protein; this process requires Fas-mediated dephosphorylation of Max. The expression of this gene is regulated by interferon-gamma and lipopolysaccharide. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]","start":104994235,"end":105023168,"strand":-1,"description":"caspase 5 [Source:HGNC Symbol;Acc:HGNC:1506]"}, {"versioned_ensembl_gene_id":"ENSG00000188801.9","gene_symbol":"ZNF322P1","gene_name":"zinc finger protein 322 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14003]","synonyms":"ZNF322B,ZNF322","biotype":"processed_pseudogene","ncbi_id":"387328","summary":null,"start":97198303,"end":97199511,"strand":-1,"description":"zinc finger protein 322 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14003]"}, {"versioned_ensembl_gene_id":"ENSG00000265626.1","gene_symbol":"AC139085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76759685,"end":76759866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278445.1","gene_symbol":"AL137246.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102903339,"end":102904000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255036.6","gene_symbol":"AL512590.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":97238497,"end":97377287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278997.1","gene_symbol":"AL662907.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33141871,"end":33143230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283679.1","gene_symbol":"AC025278.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7011884,"end":7012679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264278.1","gene_symbol":"AC027575.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76794732,"end":76822295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277117.4","gene_symbol":"FP565260.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5022493,"end":5040666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278107.1","gene_symbol":"AC027575.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76805151,"end":76805736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248713.1","gene_symbol":"AC083902.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99636529,"end":99654648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175832.12","gene_symbol":"ETV4","gene_name":"ETS variant 4 [Source:HGNC Symbol;Acc:HGNC:3493]","synonyms":"PEA3,E1AF,E1A-F","biotype":"protein_coding","ncbi_id":"2118","summary":null,"start":43527844,"end":43579620,"strand":-1,"description":"ETS variant 4 [Source:HGNC Symbol;Acc:HGNC:3493]"}, {"versioned_ensembl_gene_id":"ENSG00000235242.1","gene_symbol":"AC010982.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114122274,"end":114123293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174125.7","gene_symbol":"TLR1","gene_name":"toll like receptor 1 [Source:HGNC Symbol;Acc:HGNC:11847]","synonyms":"rsc786,KIAA0012,CD281","biotype":"protein_coding","ncbi_id":"7096","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is ubiquitously expressed, and at higher levels than other TLR genes. Different length transcripts presumably resulting from use of alternative polyadenylation site, and/or from alternative splicing, have been noted for this gene. [provided by RefSeq, Jul 2008]","start":38790677,"end":38856817,"strand":-1,"description":"toll like receptor 1 [Source:HGNC Symbol;Acc:HGNC:11847]"}, {"versioned_ensembl_gene_id":"ENSG00000153266.12","gene_symbol":"FEZF2","gene_name":"FEZ family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13506]","synonyms":"TOF,FLJ10142,FKSG36,FEZL,ZNF312,Zfp312","biotype":"protein_coding","ncbi_id":"55079","summary":null,"start":62369681,"end":62374324,"strand":-1,"description":"FEZ family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:13506]"}, {"versioned_ensembl_gene_id":"ENSG00000196589.6","gene_symbol":"MBD3L2B","gene_name":"methyl-CpG binding domain protein 3 like 2B [Source:HGNC Symbol;Acc:HGNC:53435]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729458","summary":null,"start":7018969,"end":7021450,"strand":-1,"description":"methyl-CpG binding domain protein 3 like 2B [Source:HGNC Symbol;Acc:HGNC:53435]"}, {"versioned_ensembl_gene_id":"ENSG00000283039.1","gene_symbol":"KLF18","gene_name":"Kruppel like factor 18 [Source:HGNC Symbol;Acc:HGNC:51793]","synonyms":null,"biotype":"protein_coding","ncbi_id":"105378952","summary":null,"start":44137821,"end":44141631,"strand":-1,"description":"Kruppel like factor 18 [Source:HGNC Symbol;Acc:HGNC:51793]"}, {"versioned_ensembl_gene_id":"ENSG00000100170.9","gene_symbol":"SLC5A1","gene_name":"solute carrier family 5 member 1 [Source:HGNC Symbol;Acc:HGNC:11036]","synonyms":"SGLT1,NAGT,D22S675","biotype":"protein_coding","ncbi_id":"6523","summary":"This gene encodes a member of the sodium-dependent glucose transporter (SGLT) family. The encoded integral membrane protein is the primary mediator of dietary glucose and galactose uptake from the intestinal lumen. Mutations in this gene have been associated with glucose-galactose malabsorption. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":32043032,"end":32113029,"strand":1,"description":"solute carrier family 5 member 1 [Source:HGNC Symbol;Acc:HGNC:11036]"}, {"versioned_ensembl_gene_id":"ENSG00000116525.13","gene_symbol":"TRIM62","gene_name":"tripartite motif containing 62 [Source:HGNC Symbol;Acc:HGNC:25574]","synonyms":"FLJ10759,DEAR1","biotype":"protein_coding","ncbi_id":"55223","summary":null,"start":33145402,"end":33182059,"strand":-1,"description":"tripartite motif containing 62 [Source:HGNC Symbol;Acc:HGNC:25574]"}, {"versioned_ensembl_gene_id":"ENSG00000109861.15","gene_symbol":"CTSC","gene_name":"cathepsin C [Source:HGNC Symbol;Acc:HGNC:2528]","synonyms":"PALS,DPP1,PLS","biotype":"protein_coding","ncbi_id":"1075","summary":"This gene encodes a member of the peptidase C1 family and lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in cells of the immune system. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer. A portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis. [provided by RefSeq, Nov 2015]","start":88293592,"end":88337787,"strand":-1,"description":"cathepsin C [Source:HGNC Symbol;Acc:HGNC:2528]"}, {"versioned_ensembl_gene_id":"ENSG00000254225.1","gene_symbol":"BTF3P1","gene_name":"basic transcription factor 3, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1129]","synonyms":"HUMBTFA","biotype":"processed_pseudogene","ncbi_id":"693","summary":null,"start":51721670,"end":51722164,"strand":-1,"description":"basic transcription factor 3, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1129]"}, {"versioned_ensembl_gene_id":"ENSG00000226804.4","gene_symbol":"AL359839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44150594,"end":44151753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254025.1","gene_symbol":"BRIX1P1","gene_name":"BRX1, biogenesis of ribosomes pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51527]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422268","summary":null,"start":51435602,"end":51436509,"strand":1,"description":"BRX1, biogenesis of ribosomes pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51527]"}, {"versioned_ensembl_gene_id":"ENSG00000201778.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":157153548,"end":157153640,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241395.3","gene_symbol":"RN7SL344P","gene_name":"RNA, 7SL, cytoplasmic 344, pseudogene [Source:HGNC Symbol;Acc:HGNC:46360]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480503","summary":null,"start":211792111,"end":211792406,"strand":-1,"description":"RNA, 7SL, cytoplasmic 344, pseudogene [Source:HGNC Symbol;Acc:HGNC:46360]"}, {"versioned_ensembl_gene_id":"ENSG00000199132.1","gene_symbol":"MIR450A1","gene_name":"microRNA 450a-1 [Source:HGNC Symbol;Acc:HGNC:28008]","synonyms":"MIRN450,hsa-mir-450a-1,hsa-mir-450-1,hsa-mir-450,MIRN450A1,MIRN450-1","biotype":"miRNA","ncbi_id":"554214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134540341,"end":134540431,"strand":-1,"description":"microRNA 450a-1 [Source:HGNC Symbol;Acc:HGNC:28008]"}, {"versioned_ensembl_gene_id":"ENSG00000283751.1","gene_symbol":"MIR452","gene_name":"microRNA 452 [Source:HGNC Symbol;Acc:HGNC:32054]","synonyms":"MIRN452,hsa-mir-452","biotype":"miRNA","ncbi_id":"574412","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151959628,"end":151959712,"strand":-1,"description":"microRNA 452 [Source:HGNC Symbol;Acc:HGNC:32054]"}, {"versioned_ensembl_gene_id":"ENSG00000005884.17","gene_symbol":"ITGA3","gene_name":"integrin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6139]","synonyms":"VLA3a,VCA-2,MSK18,GAP-B3,CD49c","biotype":"protein_coding","ncbi_id":"3675","summary":"The gene encodes a member of the integrin alpha chain family of proteins. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain that function as cell surface adhesion molecules. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha 3 subunit. This subunit joins with a beta 1 subunit to form an integrin that interacts with extracellular matrix proteins including members of the laminin family. Expression of this gene may be correlated with breast cancer metastasis. [provided by RefSeq, Oct 2015]","start":50055968,"end":50090481,"strand":1,"description":"integrin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6139]"}, {"versioned_ensembl_gene_id":"ENSG00000235168.1","gene_symbol":"AL078581.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149561152,"end":149563949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284064.1","gene_symbol":"MIR6834","gene_name":"microRNA 6834 [Source:HGNC Symbol;Acc:HGNC:50108]","synonyms":"hsa-mir-6834","biotype":"miRNA","ncbi_id":"102465501","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33290245,"end":33290325,"strand":1,"description":"microRNA 6834 [Source:HGNC Symbol;Acc:HGNC:50108]"}, {"versioned_ensembl_gene_id":"ENSG00000216069.1","gene_symbol":"MIR875","gene_name":"microRNA 875 [Source:HGNC Symbol;Acc:HGNC:33652]","synonyms":"MIRN875,hsa-mir-875","biotype":"miRNA","ncbi_id":"100126309","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99536786,"end":99536861,"strand":-1,"description":"microRNA 875 [Source:HGNC Symbol;Acc:HGNC:33652]"}, {"versioned_ensembl_gene_id":"ENSG00000276494.1","gene_symbol":"KCNQ1OT1_3","gene_name":"KCNQ1 overlapping transcript 1 conserved region 3 [Source:RFAM;Acc:RF01948]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2674625,"end":2674740,"strand":1,"description":"KCNQ1 overlapping transcript 1 conserved region 3 [Source:RFAM;Acc:RF01948]"}, {"versioned_ensembl_gene_id":"ENSG00000201875.1","gene_symbol":"RN7SKP178","gene_name":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479175","summary":null,"start":205900630,"end":205900958,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]"}, {"versioned_ensembl_gene_id":"ENSG00000206738.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2615124,"end":2615224,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278789.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PYPAF2,NBS1,CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54909282,"end":54945138,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000200879.1","gene_symbol":"SNORD14E","gene_name":"small nucleolar RNA, C/D box 14E [Source:HGNC Symbol;Acc:HGNC:30354]","synonyms":null,"biotype":"snoRNA","ncbi_id":"85391","summary":null,"start":123058077,"end":123058161,"strand":-1,"description":"small nucleolar RNA, C/D box 14E [Source:HGNC Symbol;Acc:HGNC:30354]"}, {"versioned_ensembl_gene_id":"ENSG00000274118.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":146311720,"end":146311822,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199716.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22867818,"end":22867917,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207180.1","gene_symbol":"RNU6-411P","gene_name":"RNA, U6 small nuclear 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:47374]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479747","summary":null,"start":71182612,"end":71182718,"strand":1,"description":"RNA, U6 small nuclear 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:47374]"}, {"versioned_ensembl_gene_id":"ENSG00000238731.1","gene_symbol":"RNU7-90P","gene_name":"RNA, U7 small nuclear 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:45624]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479060","summary":null,"start":72673503,"end":72673564,"strand":1,"description":"RNA, U7 small nuclear 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:45624]"}, {"versioned_ensembl_gene_id":"ENSG00000277572.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":14075950,"end":14076038,"strand":-1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000199629.1","gene_symbol":"RNU1-14P","gene_name":"RNA, U1 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:10139]","synonyms":"RNU1P7,U1P17","biotype":"snRNA","ncbi_id":"26859","summary":null,"start":53366058,"end":53366209,"strand":1,"description":"RNA, U1 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:10139]"}, {"versioned_ensembl_gene_id":"ENSG00000251766.1","gene_symbol":"RNA5SP518","gene_name":"RNA, 5S ribosomal pseudogene 518 [Source:HGNC Symbol;Acc:HGNC:43418]","synonyms":"RN5S518","biotype":"rRNA","ncbi_id":"100873569","summary":null,"start":10090410,"end":10090528,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 518 [Source:HGNC Symbol;Acc:HGNC:43418]"}, {"versioned_ensembl_gene_id":"ENSG00000253094.1","gene_symbol":"SNORD36","gene_name":"Small nucleolar RNA SNORD36 [Source:RFAM;Acc:RF00049]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":22803145,"end":22803224,"strand":1,"description":"Small nucleolar RNA SNORD36 [Source:RFAM;Acc:RF00049]"}, {"versioned_ensembl_gene_id":"ENSG00000251803.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17403508,"end":17403620,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200246.1","gene_symbol":"RNA5SP263","gene_name":"RNA, 5S ribosomal pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:43163]","synonyms":"RN5S263","biotype":"rRNA","ncbi_id":"106479002","summary":null,"start":32256496,"end":32256623,"strand":1,"description":"RNA, 5S ribosomal pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:43163]"}, {"versioned_ensembl_gene_id":"ENSG00000243539.3","gene_symbol":"RN7SL649P","gene_name":"RNA, 7SL, cytoplasmic 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:46665]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481100","summary":null,"start":12036740,"end":12037014,"strand":-1,"description":"RNA, 7SL, cytoplasmic 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:46665]"}, {"versioned_ensembl_gene_id":"ENSG00000200554.1","gene_symbol":"RNU6-1020P","gene_name":"RNA, U6 small nuclear 1020, pseudogene [Source:HGNC Symbol;Acc:HGNC:47983]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481503","summary":null,"start":125303920,"end":125304026,"strand":-1,"description":"RNA, U6 small nuclear 1020, pseudogene [Source:HGNC Symbol;Acc:HGNC:47983]"}, {"versioned_ensembl_gene_id":"ENSG00000167281.18","gene_symbol":"RBFOX3","gene_name":"RNA binding protein, fox-1 homolog 3 [Source:HGNC Symbol;Acc:HGNC:27097]","synonyms":"NeuN,HRNBP3,FOX-3","biotype":"protein_coding","ncbi_id":"146713","summary":"This gene encodes a member of the RNA-binding FOX protein family which is involved in the regulation of alternative splicing of pre-mRNA. The protein has an N-terminal proline-rich region, an RNA recognition motif (RRM) domain, and a C-terminal alanine-rich region. This gene produces the neuronal nuclei (NeuN) antigen that has been widely used as a marker for post-mitotic neurons. This gene has its highest expression in the central nervous system and plays a prominent role in neural tissue development and regulation of adult brain function. Mutations in this gene have been associated with numerous neurological disorders. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]","start":79089345,"end":79516148,"strand":-1,"description":"RNA binding protein, fox-1 homolog 3 [Source:HGNC Symbol;Acc:HGNC:27097]"}, {"versioned_ensembl_gene_id":"ENSG00000267137.1","gene_symbol":"AC005901.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61460224,"end":61463384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265433.1","gene_symbol":"MIR4447","gene_name":"microRNA 4447 [Source:HGNC Symbol;Acc:HGNC:41850]","synonyms":"hsa-mir-4447","biotype":"miRNA","ncbi_id":"100616485","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116850277,"end":116850367,"strand":-1,"description":"microRNA 4447 [Source:HGNC Symbol;Acc:HGNC:41850]"}, {"versioned_ensembl_gene_id":"ENSG00000221240.1","gene_symbol":"MIR1258","gene_name":"microRNA 1258 [Source:HGNC Symbol;Acc:HGNC:35323]","synonyms":"MIRN1258,hsa-mir-1258","biotype":"miRNA","ncbi_id":"100302172","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":179860836,"end":179860908,"strand":-1,"description":"microRNA 1258 [Source:HGNC Symbol;Acc:HGNC:35323]"}, {"versioned_ensembl_gene_id":"ENSG00000212161.1","gene_symbol":"SNORD64","gene_name":"Small Nucleolar RNA SNORD64 [Source:RFAM;Acc:RF00570]","synonyms":"HBII-13","biotype":"snoRNA","ncbi_id":"347686","summary":"This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]","start":159851906,"end":159851972,"strand":-1,"description":"Small Nucleolar RNA SNORD64 [Source:RFAM;Acc:RF00570]"}, {"versioned_ensembl_gene_id":"ENSG00000275411.1","gene_symbol":"MIR6882","gene_name":"microRNA 6882 [Source:HGNC Symbol;Acc:HGNC:49928]","synonyms":"hsa-mir-6882","biotype":"miRNA","ncbi_id":"102465531","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74840642,"end":74840707,"strand":-1,"description":"microRNA 6882 [Source:HGNC Symbol;Acc:HGNC:49928]"}, {"versioned_ensembl_gene_id":"ENSG00000264201.1","gene_symbol":"MIR4701","gene_name":"microRNA 4701 [Source:HGNC Symbol;Acc:HGNC:41627]","synonyms":"hsa-mir-4701","biotype":"miRNA","ncbi_id":"100616262","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48771975,"end":48772037,"strand":-1,"description":"microRNA 4701 [Source:HGNC Symbol;Acc:HGNC:41627]"}, {"versioned_ensembl_gene_id":"ENSG00000222636.1","gene_symbol":"RN7SKP54","gene_name":"RNA, 7SK small nuclear pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:45778]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080626","summary":null,"start":101058299,"end":101058567,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:45778]"}, {"versioned_ensembl_gene_id":"ENSG00000252850.1","gene_symbol":"RNU1-117P","gene_name":"RNA, U1 small nuclear 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48459]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480189","summary":null,"start":88581639,"end":88581796,"strand":1,"description":"RNA, U1 small nuclear 117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48459]"}, {"versioned_ensembl_gene_id":"ENSG00000206731.1","gene_symbol":"SNORA36","gene_name":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":27642043,"end":27642169,"strand":-1,"description":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]"}, {"versioned_ensembl_gene_id":"ENSG00000202473.1","gene_symbol":"RN7SKP81","gene_name":"RNA, 7SK small nuclear pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:45805]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480858","summary":null,"start":143090347,"end":143090677,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:45805]"}, {"versioned_ensembl_gene_id":"ENSG00000207397.1","gene_symbol":"RNU6-1179P","gene_name":"RNA, U6 small nuclear 1179, pseudogene [Source:HGNC Symbol;Acc:HGNC:48142]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480084","summary":null,"start":22555261,"end":22555367,"strand":1,"description":"RNA, U6 small nuclear 1179, pseudogene [Source:HGNC Symbol;Acc:HGNC:48142]"}, {"versioned_ensembl_gene_id":"ENSG00000222941.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":151916331,"end":151916418,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000258465.6","gene_symbol":"AL139011.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":160217464,"end":160285130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228606.2","gene_symbol":"AL139011.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160261744,"end":160262778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260046.1","gene_symbol":"AL162632.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45369215,"end":45370839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251108.1","gene_symbol":"YBX1P5","gene_name":"Y-box binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42426]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861569","summary":null,"start":72417489,"end":72418335,"strand":1,"description":"Y-box binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42426]"}, {"versioned_ensembl_gene_id":"ENSG00000261269.1","gene_symbol":"AC093278.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":72439903,"end":72442387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244061.1","gene_symbol":"AC093278.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72381794,"end":72382393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239257.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29726669,"end":29727139,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000091947.9","gene_symbol":"TMEM101","gene_name":"transmembrane protein 101 [Source:HGNC Symbol;Acc:HGNC:28653]","synonyms":"MGC4251,FLJ23987","biotype":"protein_coding","ncbi_id":"84336","summary":null,"start":44011188,"end":44023946,"strand":-1,"description":"transmembrane protein 101 [Source:HGNC Symbol;Acc:HGNC:28653]"}, {"versioned_ensembl_gene_id":"ENSG00000266711.1","gene_symbol":"AC021534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79132722,"end":79136402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178404.9","gene_symbol":"CEP295NL","gene_name":"CEP295 N-terminal like [Source:HGNC Symbol;Acc:HGNC:44659]","synonyms":"KIAA1731NL,DDC8","biotype":"protein_coding","ncbi_id":"100653515","summary":null,"start":78870910,"end":78903217,"strand":-1,"description":"CEP295 N-terminal like [Source:HGNC Symbol;Acc:HGNC:44659]"}, {"versioned_ensembl_gene_id":"ENSG00000254469.7","gene_symbol":"AP002495.1","gene_name":"Putative short transient receptor potential channel 2-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNB5]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71865509,"end":71928654,"strand":-1,"description":"Putative short transient receptor potential channel 2-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNB5]"}, {"versioned_ensembl_gene_id":"ENSG00000219553.2","gene_symbol":"AL031133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149491567,"end":149492289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204584.1","gene_symbol":"AC027801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49845910,"end":49848837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148335.14","gene_symbol":"NTMT1","gene_name":"N-terminal Xaa-Pro-Lys N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23373]","synonyms":"NRMT,METTL11A,HOMT1A,C9orf32,AD-003,NRMT1","biotype":"protein_coding","ncbi_id":"28989","summary":"The METTL11A gene encodes an N-terminal methyltransferase for the RAN (MIM 601179) guanine nucleotide exchange factor regulator of chromosome condensation 1 (RCC1; MIM 179710). METTL11A enzyme alpha-N-methylates other protein targets such as SET (MIM 600960) and RB (MIM 180200).[supplied by OMIM, Nov 2010]","start":129608884,"end":129636131,"strand":1,"description":"N-terminal Xaa-Pro-Lys N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23373]"}, {"versioned_ensembl_gene_id":"ENSG00000235142.7","gene_symbol":"LINC02532","gene_name":"long intergenic non-protein coding RNA 2532 [Source:HGNC Symbol;Acc:HGNC:53549]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100422737","summary":null,"start":106717452,"end":106787541,"strand":-1,"description":"long intergenic non-protein coding RNA 2532 [Source:HGNC Symbol;Acc:HGNC:53549]"}, {"versioned_ensembl_gene_id":"ENSG00000233985.1","gene_symbol":"LINC01681","gene_name":"long intergenic non-protein coding RNA 1681 [Source:HGNC Symbol;Acc:HGNC:52468]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371609","summary":null,"start":170174403,"end":170241287,"strand":1,"description":"long intergenic non-protein coding RNA 1681 [Source:HGNC Symbol;Acc:HGNC:52468]"}, {"versioned_ensembl_gene_id":"ENSG00000238051.1","gene_symbol":"ISCUP1","gene_name":"iron-sulfur cluster assembly enzyme pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462833","summary":null,"start":170211010,"end":170211457,"strand":-1,"description":"iron-sulfur cluster assembly enzyme pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38021]"}, {"versioned_ensembl_gene_id":"ENSG00000228692.2","gene_symbol":"AL445307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163586583,"end":163588165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226868.1","gene_symbol":"AC096637.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":211715928,"end":211725402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164187.6","gene_symbol":"LMBRD2","gene_name":"LMBR1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25287]","synonyms":"DKFZp434H2226","biotype":"protein_coding","ncbi_id":"92255","summary":null,"start":36098412,"end":36151961,"strand":-1,"description":"LMBR1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25287]"}, {"versioned_ensembl_gene_id":"ENSG00000156381.8","gene_symbol":"ANKRD9","gene_name":"ankyrin repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20096]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122416","summary":null,"start":102501760,"end":102509799,"strand":-1,"description":"ankyrin repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20096]"}, {"versioned_ensembl_gene_id":"ENSG00000237017.1","gene_symbol":"AC245052.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54119511,"end":54125343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105619.13","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"FB1,INO80F,INO80F,amida,amida,FB1","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107013,"end":54115675,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000196663.15","gene_symbol":"TECPR2","gene_name":"tectonin beta-propeller repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:19957]","synonyms":"KIAA0329","biotype":"protein_coding","ncbi_id":"9895","summary":"The protein encoded by this gene is a member of the tectonin beta-propeller repeat-containing (TECPR) family, and contains both TECPR and tryptophan-aspartic acid repeat (WD repeat) domains. This gene has been implicated in autophagy, as reduced expression levels of this gene have been associated with impaired autophagy. Recessive mutations in this gene have been associated with a hereditary form of spastic paraparesis (HSP). HSP is characterized by progressive spasticity and paralysis of the legs. There is also some evidence linking mutations in this gene with birdshot chorioretinopathy (BSCR), which results in inflammation of the choroid and retina. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":102362963,"end":102502481,"strand":1,"description":"tectonin beta-propeller repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:19957]"}, {"versioned_ensembl_gene_id":"ENSG00000278925.1","gene_symbol":"AC005753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141825708,"end":141826325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254972.1","gene_symbol":"AP003498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71701268,"end":71705404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245248.7","gene_symbol":"USP2-AS1","gene_name":"USP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48673]","synonyms":"THY1-AS1","biotype":"antisense_RNA","ncbi_id":"100499227","summary":null,"start":119381778,"end":119526664,"strand":1,"description":"USP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48673]"}, {"versioned_ensembl_gene_id":"ENSG00000230676.1","gene_symbol":"AL353803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129430652,"end":129451422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233273.1","gene_symbol":"AMMECR1LP1","gene_name":"AMMECR1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39809]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420921","summary":null,"start":96573659,"end":96574499,"strand":1,"description":"AMMECR1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39809]"}, {"versioned_ensembl_gene_id":"ENSG00000216265.1","gene_symbol":"FABP12P1","gene_name":"fatty acid binding protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479057","summary":null,"start":149304107,"end":149304428,"strand":-1,"description":"fatty acid binding protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45176]"}, {"versioned_ensembl_gene_id":"ENSG00000249480.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"bPG116M5.10,STK19P,RP2","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":31995452,"end":31995969,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000219409.2","gene_symbol":"AL590704.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144397959,"end":144398752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220739.2","gene_symbol":"AL513475.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144708106,"end":144708497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253972.5","gene_symbol":"MAL2","gene_name":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"114569","summary":"This gene encodes a multispan transmembrane protein belonging to the MAL proteolipid family. The protein is a component of lipid rafts and, in polarized cells, it primarily localizes to endosomal structures beneath the apical membrane. It is required for transcytosis, an intracellular transport pathway used to deliver membrane-bound proteins and exogenous cargos from the basolateral to the apical surface. [provided by RefSeq, Jul 2008]","start":119215111,"end":119246848,"strand":-1,"description":"mal, T-cell differentiation protein 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13634]"}, {"versioned_ensembl_gene_id":"ENSG00000225311.1","gene_symbol":"AL024474.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144311699,"end":144333301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238110.1","gene_symbol":"AL353572.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87944276,"end":87945023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170385.9","gene_symbol":"SLC30A1","gene_name":"solute carrier family 30 member 1 [Source:HGNC Symbol;Acc:HGNC:11012]","synonyms":"ZRC1,ZNT1","biotype":"protein_coding","ncbi_id":"7779","summary":null,"start":211571568,"end":211578742,"strand":-1,"description":"solute carrier family 30 member 1 [Source:HGNC Symbol;Acc:HGNC:11012]"}, {"versioned_ensembl_gene_id":"ENSG00000204572.9","gene_symbol":"KRTAP5-10","gene_name":"keratin associated protein 5-10 [Source:HGNC Symbol;Acc:HGNC:23605]","synonyms":"KRTAP5.10","biotype":"protein_coding","ncbi_id":"387273","summary":null,"start":71565563,"end":71566738,"strand":1,"description":"keratin associated protein 5-10 [Source:HGNC Symbol;Acc:HGNC:23605]"}, {"versioned_ensembl_gene_id":"ENSG00000055147.18","gene_symbol":"FAM114A2","gene_name":"family with sequence similarity 114 member A2 [Source:HGNC Symbol;Acc:HGNC:1333]","synonyms":"C5orf3,133K02","biotype":"protein_coding","ncbi_id":"10827","summary":null,"start":153990128,"end":154038936,"strand":-1,"description":"family with sequence similarity 114 member A2 [Source:HGNC Symbol;Acc:HGNC:1333]"}, {"versioned_ensembl_gene_id":"ENSG00000250529.1","gene_symbol":"LINC02121","gene_name":"long intergenic non-protein coding RNA 2121 [Source:HGNC Symbol;Acc:HGNC:52977]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374631","summary":null,"start":5069192,"end":5078311,"strand":-1,"description":"long intergenic non-protein coding RNA 2121 [Source:HGNC Symbol;Acc:HGNC:52977]"}, {"versioned_ensembl_gene_id":"ENSG00000284237.1","gene_symbol":"AL356275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207959292,"end":207969329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251426.1","gene_symbol":"AC010451.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5046796,"end":5049497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250481.1","gene_symbol":"AC010451.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4974690,"end":5034267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251506.1","gene_symbol":"AC010451.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4967764,"end":4970425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134825.15","gene_symbol":"TMEM258","gene_name":"transmembrane protein 258 [Source:HGNC Symbol;Acc:HGNC:1164]","synonyms":"C11orf10","biotype":"protein_coding","ncbi_id":"746","summary":null,"start":61768501,"end":61792802,"strand":-1,"description":"transmembrane protein 258 [Source:HGNC Symbol;Acc:HGNC:1164]"}, {"versioned_ensembl_gene_id":"ENSG00000243199.1","gene_symbol":"AC115223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65573459,"end":65574328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165632.7","gene_symbol":"TAF3","gene_name":"TATA-box binding protein associated factor 3 [Source:HGNC Symbol;Acc:HGNC:17303]","synonyms":"TAFII140,TAF140","biotype":"protein_coding","ncbi_id":"83860","summary":"The highly conserved RNA polymerase II transcription factor TFIID (see TAF1; MIM 313650) comprises the TATA box-binding protein (TBP; MIM 600075) and a set of TBP-associated factors (TAFs), including TAF3. TAFs contribute to promoter recognition and selectivity and act as antiapoptotic factors (Gangloff et al., 2001 [PubMed 11438666]).[supplied by OMIM, May 2009]","start":7818504,"end":8016627,"strand":1,"description":"TATA-box binding protein associated factor 3 [Source:HGNC Symbol;Acc:HGNC:17303]"}, {"versioned_ensembl_gene_id":"ENSG00000251371.1","gene_symbol":"AC010634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4640731,"end":4648254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248311.1","gene_symbol":"AC026719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4775476,"end":4805769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267682.1","gene_symbol":"AC016590.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37337236,"end":37337743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248467.1","gene_symbol":"AC026719.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4831699,"end":4849800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249521.1","gene_symbol":"LINC02114","gene_name":"long intergenic non-protein coding RNA 2114 [Source:HGNC Symbol;Acc:HGNC:52968]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929153","summary":null,"start":4773481,"end":4774865,"strand":1,"description":"long intergenic non-protein coding RNA 2114 [Source:HGNC Symbol;Acc:HGNC:52968]"}, {"versioned_ensembl_gene_id":"ENSG00000243444.7","gene_symbol":"PALM2","gene_name":"paralemmin 2 [Source:HGNC Symbol;Acc:HGNC:15845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114299","summary":null,"start":109640788,"end":109946703,"strand":1,"description":"paralemmin 2 [Source:HGNC Symbol;Acc:HGNC:15845]"}, {"versioned_ensembl_gene_id":"ENSG00000251616.1","gene_symbol":"AC113410.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133111055,"end":133114475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127831.10","gene_symbol":"VIL1","gene_name":"villin 1 [Source:HGNC Symbol;Acc:HGNC:12690]","synonyms":"VIL,D2S1471","biotype":"protein_coding","ncbi_id":"7429","summary":"This gene encodes a member of a family of calcium-regulated actin-binding proteins. This protein represents a dominant part of the brush border cytoskeleton which functions in the capping, severing, and bundling of actin filaments. Two mRNAs of 2.7 kb and 3.5 kb have been observed; they result from utilization of alternate poly-adenylation signals present in the terminal exon. [provided by RefSeq, Jul 2008]","start":218419092,"end":218453295,"strand":1,"description":"villin 1 [Source:HGNC Symbol;Acc:HGNC:12690]"}, {"versioned_ensembl_gene_id":"ENSG00000082512.14","gene_symbol":"TRAF5","gene_name":"TNF receptor associated factor 5 [Source:HGNC Symbol;Acc:HGNC:12035]","synonyms":"RNF84","biotype":"protein_coding","ncbi_id":"7188","summary":"The scaffold protein encoded by this gene is a member of the tumor necrosis factor receptor-associated factor (TRAF) protein family and contains a meprin and TRAF homology (MATH) domain, a RING-type zinc finger, and two TRAF-type zinc fingers. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. This protein is one of the components of a multiple protein complex which binds to tumor necrosis factor (TNF) receptor cytoplasmic domains and mediates TNF-induced activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":211326615,"end":211374946,"strand":1,"description":"TNF receptor associated factor 5 [Source:HGNC Symbol;Acc:HGNC:12035]"}, {"versioned_ensembl_gene_id":"ENSG00000247572.7","gene_symbol":"CKMT2-AS1","gene_name":"CKMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48997]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131067","summary":null,"start":81204084,"end":81301560,"strand":-1,"description":"CKMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48997]"}, {"versioned_ensembl_gene_id":"ENSG00000248794.1","gene_symbol":"AC026436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81242330,"end":81242599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222000.7","gene_symbol":"AC092675.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98331389,"end":98356005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215223.3","gene_symbol":"CYP51A1P3","gene_name":"cytochrome P450 family 51 subfamily A member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41991]","synonyms":"CYP51P3","biotype":"processed_pseudogene","ncbi_id":"100422264","summary":null,"start":148478693,"end":148480763,"strand":1,"description":"cytochrome P450 family 51 subfamily A member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41991]"}, {"versioned_ensembl_gene_id":"ENSG00000248597.1","gene_symbol":"AC126768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1963609,"end":1967154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249731.1","gene_symbol":"AC126768.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1968094,"end":1969013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168496.3","gene_symbol":"FEN1","gene_name":"flap structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3650]","synonyms":"RAD2,MF1,FEN-1","biotype":"protein_coding","ncbi_id":"2237","summary":"The protein encoded by this gene removes 5' overhanging flaps in DNA repair and processes the 5' ends of Okazaki fragments in lagging strand DNA synthesis. Direct physical interaction between this protein and AP endonuclease 1 during long-patch base excision repair provides coordinated loading of the proteins onto the substrate, thus passing the substrate from one enzyme to another. The protein is a member of the XPG/RAD2 endonuclease family and is one of ten proteins essential for cell-free DNA replication. DNA secondary structure can inhibit flap processing at certain trinucleotide repeats in a length-dependent manner by concealing the 5' end of the flap that is necessary for both binding and cleavage by the protein encoded by this gene. Therefore, secondary structure can deter the protective function of this protein, leading to site-specific trinucleotide expansions. [provided by RefSeq, Jul 2008]","start":61792637,"end":61797244,"strand":1,"description":"flap structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3650]"}, {"versioned_ensembl_gene_id":"ENSG00000217027.1","gene_symbol":"TPT1P4","gene_name":"tumor protein, translationally-controlled 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285741","summary":null,"start":144200447,"end":144200965,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49298]"}, {"versioned_ensembl_gene_id":"ENSG00000277060.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54894717,"end":54929555,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000170464.9","gene_symbol":"DNAJC18","gene_name":"DnaJ heat shock protein family (Hsp40) member C18 [Source:HGNC Symbol;Acc:HGNC:28429]","synonyms":"MGC29463","biotype":"protein_coding","ncbi_id":"202052","summary":null,"start":139408588,"end":139444491,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C18 [Source:HGNC Symbol;Acc:HGNC:28429]"}, {"versioned_ensembl_gene_id":"ENSG00000127184.12","gene_symbol":"COX7C","gene_name":"cytochrome c oxidase subunit 7C [Source:HGNC Symbol;Acc:HGNC:2292]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1350","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes subunit VIIc, which shares 87% and 85% amino acid sequence identity with mouse and bovine COX VIIc, respectively, and is found in all tissues. A pseudogene COX7CP1 has been found on chromosome 13. [provided by RefSeq, Jul 2008]","start":86617904,"end":86620962,"strand":1,"description":"cytochrome c oxidase subunit 7C [Source:HGNC Symbol;Acc:HGNC:2292]"}, {"versioned_ensembl_gene_id":"ENSG00000275198.1","gene_symbol":"AL512791.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90383365,"end":90387973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266809.1","gene_symbol":"AC022884.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24689914,"end":24690161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118515.11","gene_symbol":"SGK1","gene_name":"serum/glucocorticoid regulated kinase 1 [Source:HGNC Symbol;Acc:HGNC:10810]","synonyms":"SGK","biotype":"protein_coding","ncbi_id":"6446","summary":"This gene encodes a serine/threonine protein kinase that plays an important role in cellular stress response. This kinase activates certain potassium, sodium, and chloride channels, suggesting an involvement in the regulation of processes such as cell survival, neuronal excitability, and renal sodium excretion. High levels of expression of this gene may contribute to conditions such as hypertension and diabetic nephropathy. Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]","start":134169246,"end":134318112,"strand":-1,"description":"serum/glucocorticoid regulated kinase 1 [Source:HGNC Symbol;Acc:HGNC:10810]"}, {"versioned_ensembl_gene_id":"ENSG00000213397.10","gene_symbol":"HAUS7","gene_name":"HAUS augmin like complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:32979]","synonyms":"UIP1,UCHL5IP","biotype":"protein_coding","ncbi_id":"55559","summary":"This gene encodes a subunit of the augmin complex, which regulates centrosome and mitotic spindle integrity, and is necessary for the completion of cytokinesis. The encoded protein was identified by interaction with ubiquitin C-terminal hydrolase 37. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":153447666,"end":153495516,"strand":-1,"description":"HAUS augmin like complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:32979]"}, {"versioned_ensembl_gene_id":"ENSG00000249349.1","gene_symbol":"AC114928.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85112342,"end":85112756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182224.11","gene_symbol":"CYB5D1","gene_name":"cytochrome b5 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26516]","synonyms":"FLJ32499","biotype":"protein_coding","ncbi_id":"124637","summary":null,"start":7857746,"end":7862282,"strand":1,"description":"cytochrome b5 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26516]"}, {"versioned_ensembl_gene_id":"ENSG00000226986.4","gene_symbol":"AC092017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211207239,"end":211207897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067221.13","gene_symbol":"STOML1","gene_name":"stomatin like 1 [Source:HGNC Symbol;Acc:HGNC:14560]","synonyms":"STORP,SLP-1,hUNC-24,FLJ36370","biotype":"protein_coding","ncbi_id":"9399","summary":null,"start":73978923,"end":73994622,"strand":-1,"description":"stomatin like 1 [Source:HGNC Symbol;Acc:HGNC:14560]"}, {"versioned_ensembl_gene_id":"ENSG00000214897.4","gene_symbol":"PNMA6E","gene_name":"paraneoplastic Ma antigen family member 6E [Source:HGNC Symbol;Acc:HGNC:50767]","synonyms":null,"biotype":"protein_coding","ncbi_id":"649238","summary":null,"start":153395640,"end":153401420,"strand":-1,"description":"paraneoplastic Ma antigen family member 6E [Source:HGNC Symbol;Acc:HGNC:50767]"}, {"versioned_ensembl_gene_id":"ENSG00000070159.13","gene_symbol":"PTPN3","gene_name":"protein tyrosine phosphatase, non-receptor type 3 [Source:HGNC Symbol;Acc:HGNC:9655]","synonyms":"PTPH1","biotype":"protein_coding","ncbi_id":"5774","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This protein contains a C-terminal PTP domain and an N-terminal domain homologous to the band 4.1 superfamily of cytoskeletal-associated proteins. P97, a cell cycle regulator involved in a variety of membrane related functions, has been shown to be a substrate of this PTP. This PTP was also found to interact with, and be regulated by adaptor protein 14-3-3 beta. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":109375466,"end":109498313,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 3 [Source:HGNC Symbol;Acc:HGNC:9655]"}, {"versioned_ensembl_gene_id":"ENSG00000255552.7","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31711771,"end":31714065,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000236022.6","gene_symbol":"AC106017.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19203825,"end":19214045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261335.1","gene_symbol":"AC005837.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76671942,"end":76673658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253274.1","gene_symbol":"IGHV1-67","gene_name":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28463","summary":null,"start":106680603,"end":106681042,"strand":-1,"description":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]"}, {"versioned_ensembl_gene_id":"ENSG00000230541.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"processed_transcript","ncbi_id":"102723346","summary":null,"start":30935539,"end":30944421,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000265639.1","gene_symbol":"AC090415.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71028770,"end":71033056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265781.1","gene_symbol":"AC090415.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71000477,"end":71011490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229284.4","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"C6orf37,bCX105N19.6,PBLT","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":30930561,"end":30943780,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000270909.1","gene_symbol":"CR788268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41979352,"end":41983753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278803.1","gene_symbol":"AC236972.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153276841,"end":153277803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231600.1","gene_symbol":"AC236972.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153249115,"end":153249691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132510.10","gene_symbol":"KDM6B","gene_name":"lysine demethylase 6B [Source:HGNC Symbol;Acc:HGNC:29012]","synonyms":"KIAA0346,JMJD3","biotype":"protein_coding","ncbi_id":"23135","summary":"The protein encoded by this gene is a lysine-specific demethylase that specifically demethylates di- or tri-methylated lysine 27 of histone H3 (H3K27me2 or H3K27me3). H3K27 trimethylation is a repressive epigenetic mark controlling chromatin organization and gene silencing. This protein can also demethylate non-histone proteins such as retinoblastoma protein. Through its demethylation actvity this gene influences cellular differentiation and development, tumorigenesis, inflammatory diseases, and neurodegenerative diseases. This protein has two classical nuclear localization signals at its N-terminus. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]","start":7839904,"end":7854796,"strand":1,"description":"lysine demethylase 6B [Source:HGNC Symbol;Acc:HGNC:29012]"}, {"versioned_ensembl_gene_id":"ENSG00000198681.6","gene_symbol":"MAGEA1","gene_name":"MAGE family member A1 [Source:HGNC Symbol;Acc:HGNC:6796]","synonyms":"MGC9326,MAGE1,CT1.1","biotype":"protein_coding","ncbi_id":"4100","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]","start":153179285,"end":153183880,"strand":1,"description":"MAGE family member A1 [Source:HGNC Symbol;Acc:HGNC:6796]"}, {"versioned_ensembl_gene_id":"ENSG00000161544.9","gene_symbol":"CYGB","gene_name":"cytoglobin [Source:HGNC Symbol;Acc:HGNC:16505]","synonyms":"STAP,HGB","biotype":"protein_coding","ncbi_id":"114757","summary":"This gene encodes a globin protein found in vertebrate cells. The encoded protein is described as a hexacoordinate hemoglobin which binds ligand differently from the pentacoordinate hemoglobins involved in oxygen transport, and may be involved in protection during oxidative stress. This gene is located on chromosome 17 in the same region as a retinal gene which is mutated in progressive rod-cone degeneration, but in the opposite orientation. [provided by RefSeq, Jan 2012]","start":76527356,"end":76551175,"strand":-1,"description":"cytoglobin [Source:HGNC Symbol;Acc:HGNC:16505]"}, {"versioned_ensembl_gene_id":"ENSG00000267033.1","gene_symbol":"AC020911.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16186276,"end":16189458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115009.11","gene_symbol":"CCL20","gene_name":"C-C motif chemokine ligand 20 [Source:HGNC Symbol;Acc:HGNC:10619]","synonyms":"MIP-3a,LARC,exodus-1,CKb4,ST38,SCYA20","biotype":"protein_coding","ncbi_id":"6364","summary":"This antimicrobial gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The protein encoded by this gene displays chemotactic activity for lymphocytes and can repress proliferation of myeloid progenitors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":227813842,"end":227817564,"strand":1,"description":"C-C motif chemokine ligand 20 [Source:HGNC Symbol;Acc:HGNC:10619]"}, {"versioned_ensembl_gene_id":"ENSG00000233308.1","gene_symbol":"OSTN-AS1","gene_name":"OSTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41250]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480738","summary":null,"start":191213291,"end":191234605,"strand":-1,"description":"OSTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41250]"}, {"versioned_ensembl_gene_id":"ENSG00000229172.1","gene_symbol":"AC073065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227801840,"end":227804705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230310.1","gene_symbol":"AC010422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12552597,"end":12553644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141698.16","gene_symbol":"NT5C3B","gene_name":"5'-nucleotidase, cytosolic IIIB [Source:HGNC Symbol;Acc:HGNC:28300]","synonyms":"cN-IIIB,NT5C3L,MGC20781","biotype":"protein_coding","ncbi_id":"115024","summary":null,"start":41825181,"end":41836263,"strand":-1,"description":"5'-nucleotidase, cytosolic IIIB [Source:HGNC Symbol;Acc:HGNC:28300]"}, {"versioned_ensembl_gene_id":"ENSG00000235275.3","gene_symbol":"KRT18P16","gene_name":"keratin 18 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:33384]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391827","summary":null,"start":123636110,"end":123637403,"strand":1,"description":"keratin 18 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:33384]"}, {"versioned_ensembl_gene_id":"ENSG00000251018.2","gene_symbol":"HMMR-AS1","gene_name":"HMMR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49149]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927813","summary":null,"start":163483065,"end":163494058,"strand":-1,"description":"HMMR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49149]"}, {"versioned_ensembl_gene_id":"ENSG00000275297.1","gene_symbol":"AL162731.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":41760088,"end":41764175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274104.1","gene_symbol":"AC020910.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34733298,"end":34733837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140153.17","gene_symbol":"WDR20","gene_name":"WD repeat domain 20 [Source:HGNC Symbol;Acc:HGNC:19667]","synonyms":"MGC33177,FLJ33659,DMR","biotype":"protein_coding","ncbi_id":"91833","summary":"This gene encodes a WD repeat-containing protein that functions to preserve and regulate the activity of the USP12-UAF1 deubiquitinating enzyme complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011]","start":102139503,"end":102224847,"strand":1,"description":"WD repeat domain 20 [Source:HGNC Symbol;Acc:HGNC:19667]"}, {"versioned_ensembl_gene_id":"ENSG00000188613.6","gene_symbol":"NANOS1","gene_name":"nanos C2HC-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:23044]","synonyms":"ZC2HC12A,NOS1","biotype":"protein_coding","ncbi_id":"340719","summary":"This gene encodes a CCHC-type zinc finger protein that is a member of the nanos family. This protein co-localizes with the RNA-binding protein pumilio RNA-binding family member 2 and may be involved in regulating translation as a post-transcriptional repressor. Mutations in this gene are associated with spermatogenic impairment. [provided by RefSeq, Sep 2015]","start":119029716,"end":119033732,"strand":1,"description":"nanos C2HC-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:23044]"}, {"versioned_ensembl_gene_id":"ENSG00000132341.11","gene_symbol":"RAN","gene_name":"RAN, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9846]","synonyms":"Gsp1,ARA24,TC4","biotype":"protein_coding","ncbi_id":"5901","summary":"RAN (ras-related nuclear protein) is a small GTP binding protein belonging to the RAS superfamily that is essential for the translocation of RNA and proteins through the nuclear pore complex. The RAN protein is also involved in control of DNA synthesis and cell cycle progression. Nuclear localization of RAN requires the presence of regulator of chromosome condensation 1 (RCC1). Mutations in RAN disrupt DNA synthesis. Because of its many functions, it is likely that RAN interacts with several other proteins. RAN regulates formation and organization of the microtubule network independently of its role in the nucleus-cytosol exchange of macromolecules. RAN could be a key signaling molecule regulating microtubule polymerization during mitosis. RCC1 generates a high local concentration of RAN-GTP around chromatin which, in turn, induces the local nucleation of microtubules. RAN is an androgen receptor (AR) coactivator that binds differentially with different lengths of polyglutamine within the androgen receptor. Polyglutamine repeat expansion in the AR is linked to Kennedy's disease (X-linked spinal and bulbar muscular atrophy). RAN coactivation of the AR diminishes with polyglutamine expansion within the AR, and this weak coactivation may lead to partial androgen insensitivity during the development of Kennedy's disease. [provided by RefSeq, Jul 2008]","start":130871879,"end":130877678,"strand":1,"description":"RAN, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9846]"}, {"versioned_ensembl_gene_id":"ENSG00000269919.1","gene_symbol":"AL022067.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":106100140,"end":106100593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136828.18","gene_symbol":"RALGPS1","gene_name":"Ral GEF with PH domain and SH3 binding motif 1 [Source:HGNC Symbol;Acc:HGNC:16851]","synonyms":"RALGPS1A,RALGEF2,KIAA0351","biotype":"protein_coding","ncbi_id":"9649","summary":null,"start":126914774,"end":127223166,"strand":1,"description":"Ral GEF with PH domain and SH3 binding motif 1 [Source:HGNC Symbol;Acc:HGNC:16851]"}, {"versioned_ensembl_gene_id":"ENSG00000226197.2","gene_symbol":"AL583785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13446491,"end":13487511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225437.5","gene_symbol":"PACRG-AS2","gene_name":"PACRG antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40871]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929239","summary":null,"start":163042557,"end":163054161,"strand":-1,"description":"PACRG antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40871]"}, {"versioned_ensembl_gene_id":"ENSG00000275475.1","gene_symbol":"IGHV3-54","gene_name":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28419","summary":null,"start":106601346,"end":106601792,"strand":-1,"description":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]"}, {"versioned_ensembl_gene_id":"ENSG00000253714.1","gene_symbol":"IGHVII-53-1","gene_name":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]","synonyms":"IGHV(II)-53-1","biotype":"IG_V_pseudogene","ncbi_id":"28362","summary":null,"start":106599670,"end":106599924,"strand":-1,"description":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]"}, {"versioned_ensembl_gene_id":"ENSG00000167644.11","gene_symbol":"C19orf33","gene_name":"chromosome 19 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:16668]","synonyms":"IMUP-2,IMUP-1,IMUP,H2RSP","biotype":"protein_coding","ncbi_id":"64073","summary":"The protein encoded by this gene has been shown to be upregulated in SV40-immortalized fibroblasts as well as in endometrial carcinoma cells. The encoded protein is found primarily in the nucleus. This protein may play a role in placental development and diseases such as pre-eclampsia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":38304161,"end":38305009,"strand":1,"description":"chromosome 19 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:16668]"}, {"versioned_ensembl_gene_id":"ENSG00000253941.1","gene_symbol":"IGHVII-51-2","gene_name":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]","synonyms":"IGHV(II)-51-2","biotype":"IG_V_pseudogene","ncbi_id":"28363","summary":null,"start":106584718,"end":106584976,"strand":-1,"description":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]"}, {"versioned_ensembl_gene_id":"ENSG00000253545.1","gene_symbol":"IGHV3-52","gene_name":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28421","summary":null,"start":106586376,"end":106586826,"strand":-1,"description":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]"}, {"versioned_ensembl_gene_id":"ENSG00000176915.14","gene_symbol":"ANKLE2","gene_name":"ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29101]","synonyms":"KIAA0692,LEMD7,Lem4","biotype":"protein_coding","ncbi_id":"23141","summary":"This gene encodes a member of the LEM family of inner nuclear membrane proteins. The encoded protein functions as a mitotic regulator through postmitotic formation of the nuclear envelope. Mutations in this gene cause morphology defects in the nuclear envelope and BAF hyperphosphorylation. [provided by RefSeq, Mar 2014]","start":132725503,"end":132761888,"strand":-1,"description":"ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29101]"}, {"versioned_ensembl_gene_id":"ENSG00000253241.1","gene_symbol":"IGHV3-50","gene_name":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28422","summary":null,"start":106566117,"end":106566555,"strand":-1,"description":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]"}, {"versioned_ensembl_gene_id":"ENSG00000229092.2","gene_symbol":"IGHV3-47","gene_name":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28425","summary":null,"start":106518582,"end":106519027,"strand":-1,"description":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]"}, {"versioned_ensembl_gene_id":"ENSG00000228546.2","gene_symbol":"AC091390.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102337316,"end":102339115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253895.1","gene_symbol":"IGHVII-44-2","gene_name":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]","synonyms":"IGHV(II)-44-2","biotype":"IG_V_pseudogene","ncbi_id":"28366","summary":null,"start":106494134,"end":106494383,"strand":-1,"description":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]"}, {"versioned_ensembl_gene_id":"ENSG00000089335.20","gene_symbol":"ZNF302","gene_name":"zinc finger protein 302 [Source:HGNC Symbol;Acc:HGNC:13848]","synonyms":"ZNF327,ZNF140L,ZNF135L","biotype":"protein_coding","ncbi_id":"55900","summary":"This gene encodes a member of the zinc-finger protein family. The encoded protein contains seven C2H2-type zinc fingers and a KRAB domain, but its function has yet to be determined. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2014]","start":34677639,"end":34686397,"strand":1,"description":"zinc finger protein 302 [Source:HGNC Symbol;Acc:HGNC:13848]"}, {"versioned_ensembl_gene_id":"ENSG00000228737.2","gene_symbol":"AC008781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141618414,"end":141626481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254383.1","gene_symbol":"AC048387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40900016,"end":40901854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171202.6","gene_symbol":"TMEM126A","gene_name":"transmembrane protein 126A [Source:HGNC Symbol;Acc:HGNC:25382]","synonyms":"OPA7,DKFZp586C1924","biotype":"protein_coding","ncbi_id":"84233","summary":"The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":85647967,"end":85656547,"strand":1,"description":"transmembrane protein 126A [Source:HGNC Symbol;Acc:HGNC:25382]"}, {"versioned_ensembl_gene_id":"ENSG00000145907.14","gene_symbol":"G3BP1","gene_name":"G3BP stress granule assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30292]","synonyms":"HDH-VIII,G3BP","biotype":"protein_coding","ncbi_id":"10146","summary":"This gene encodes one of the DNA-unwinding enzymes which prefers partially unwound 3'-tailed substrates and can also unwind partial RNA/DNA and RNA/RNA duplexes in an ATP-dependent fashion. This enzyme is a member of the heterogeneous nuclear RNA-binding proteins and is also an element of the Ras signal transduction pathway. It binds specifically to the Ras-GTPase-activating protein by associating with its SH3 domain. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":151771045,"end":151812785,"strand":1,"description":"G3BP stress granule assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30292]"}, {"versioned_ensembl_gene_id":"ENSG00000139540.11","gene_symbol":"SLC39A5","gene_name":"solute carrier family 39 member 5 [Source:HGNC Symbol;Acc:HGNC:20502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283375","summary":"The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":56230049,"end":56237846,"strand":1,"description":"solute carrier family 39 member 5 [Source:HGNC Symbol;Acc:HGNC:20502]"}, {"versioned_ensembl_gene_id":"ENSG00000254228.2","gene_symbol":"IGHV3-42","gene_name":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28427","summary":null,"start":106463256,"end":106463691,"strand":-1,"description":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]"}, {"versioned_ensembl_gene_id":"ENSG00000273228.1","gene_symbol":"AP002826.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57029408,"end":57029722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227625.2","gene_symbol":"AL359510.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":228134785,"end":228134992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155890.3","gene_symbol":"TRIM42","gene_name":"tripartite motif containing 42 [Source:HGNC Symbol;Acc:HGNC:19014]","synonyms":"T4A1,PPP1R40,FLJ40097","biotype":"protein_coding","ncbi_id":"287015","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, namely a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]","start":140678039,"end":140701150,"strand":1,"description":"tripartite motif containing 42 [Source:HGNC Symbol;Acc:HGNC:19014]"}, {"versioned_ensembl_gene_id":"ENSG00000165782.10","gene_symbol":"TMEM55B","gene_name":"transmembrane protein 55B [Source:HGNC Symbol;Acc:HGNC:19299]","synonyms":"MGC26684,C14orf9","biotype":"protein_coding","ncbi_id":"90809","summary":"TMEM55B catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]","start":20457719,"end":20461612,"strand":-1,"description":"transmembrane protein 55B [Source:HGNC Symbol;Acc:HGNC:19299]"}, {"versioned_ensembl_gene_id":"ENSG00000226876.2","gene_symbol":"AC092801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":246108626,"end":246113866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147724.11","gene_symbol":"FAM135B","gene_name":"family with sequence similarity 135 member B [Source:HGNC Symbol;Acc:HGNC:28029]","synonyms":"C8ORFK32","biotype":"protein_coding","ncbi_id":"51059","summary":null,"start":138130023,"end":138496822,"strand":-1,"description":"family with sequence similarity 135 member B [Source:HGNC Symbol;Acc:HGNC:28029]"}, {"versioned_ensembl_gene_id":"ENSG00000204316.12","gene_symbol":"MRPL38","gene_name":"mitochondrial ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:14033]","synonyms":"HSPC262,RPML3,MRP-L3,MGC4810","biotype":"protein_coding","ncbi_id":"64978","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":75898643,"end":75905413,"strand":-1,"description":"mitochondrial ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:14033]"}, {"versioned_ensembl_gene_id":"ENSG00000236116.1","gene_symbol":"AC064853.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":227616998,"end":227617790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284704.1","gene_symbol":"AC064853.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227614538,"end":227614840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231099.1","gene_symbol":"BMS1P19","gene_name":"BMS1, ribosome biogenesis factor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49163]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131577","summary":null,"start":109667128,"end":109668002,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49163]"}, {"versioned_ensembl_gene_id":"ENSG00000274658.1","gene_symbol":"TBC1D3J","gene_name":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100510707","summary":null,"start":36450146,"end":36457535,"strand":-1,"description":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]"}, {"versioned_ensembl_gene_id":"ENSG00000111361.12","gene_symbol":"EIF2B1","gene_name":"eukaryotic translation initiation factor 2B subunit alpha [Source:HGNC Symbol;Acc:HGNC:3257]","synonyms":"EIF2BA,EIF2B,EIF-2Balpha,EIF-2B","biotype":"protein_coding","ncbi_id":"1967","summary":"This gene encodes one of five subunits of eukaryotic translation initiation factor 2B (EIF2B), a GTP exchange factor for eukaryotic initiation factor 2 and an essential regulator for protein synthesis. Mutations in this gene and the genes encoding other EIF2B subunits have been associated with leukoencephalopathy with vanishing white matter. [provided by RefSeq, Oct 2009]","start":123620406,"end":123633766,"strand":-1,"description":"eukaryotic translation initiation factor 2B subunit alpha [Source:HGNC Symbol;Acc:HGNC:3257]"}, {"versioned_ensembl_gene_id":"ENSG00000231199.2","gene_symbol":"MTND5P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873270","summary":null,"start":235538052,"end":235539845,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]"}, {"versioned_ensembl_gene_id":"ENSG00000253669.3","gene_symbol":"AP003356.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102805517,"end":102809971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278850.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"cl-5,nkat4b,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54849551,"end":54866326,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000197070.13","gene_symbol":"ARRDC1","gene_name":"arrestin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28633]","synonyms":"MGC40555","biotype":"protein_coding","ncbi_id":"92714","summary":null,"start":137605654,"end":137615360,"strand":1,"description":"arrestin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28633]"}, {"versioned_ensembl_gene_id":"ENSG00000233483.2","gene_symbol":"AC008105.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45245186,"end":45248836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230958.1","gene_symbol":"AC093166.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111865798,"end":111866405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235042.1","gene_symbol":"AC098820.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216385288,"end":216412696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241520.1","gene_symbol":"AC098820.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216483032,"end":216487196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163412.12","gene_symbol":"EIF4E3","gene_name":"eukaryotic translation initiation factor 4E family member 3 [Source:HGNC Symbol;Acc:HGNC:31837]","synonyms":"MGC39820","biotype":"protein_coding","ncbi_id":"317649","summary":"EIF4E3 belongs to the EIF4E family of translational initiation factors that interact with the 5-prime cap structure of mRNA and recruit mRNA to the ribosome (Joshi et al., 2004 [PubMed 15153109]).[supplied by OMIM, Mar 2008]","start":71675416,"end":71754773,"strand":-1,"description":"eukaryotic translation initiation factor 4E family member 3 [Source:HGNC Symbol;Acc:HGNC:31837]"}, {"versioned_ensembl_gene_id":"ENSG00000112658.7","gene_symbol":"SRF","gene_name":"serum response factor [Source:HGNC Symbol;Acc:HGNC:11291]","synonyms":"MCM1","biotype":"protein_coding","ncbi_id":"6722","summary":"This gene encodes a ubiquitous nuclear protein that stimulates both cell proliferation and differentiation. It is a member of the MADS (MCM1, Agamous, Deficiens, and SRF) box superfamily of transcription factors. This protein binds to the serum response element (SRE) in the promoter region of target genes. This protein regulates the activity of many immediate-early genes, for example c-fos, and thereby participates in cell cycle regulation, apoptosis, cell growth, and cell differentiation. This gene is the downstream target of many pathways; for example, the mitogen-activated protein kinase pathway (MAPK) that acts through the ternary complex factors (TCFs). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":43171299,"end":43181507,"strand":1,"description":"serum response factor [Source:HGNC Symbol;Acc:HGNC:11291]"}, {"versioned_ensembl_gene_id":"ENSG00000157045.8","gene_symbol":"NTAN1","gene_name":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123803","summary":"The protein encoded by this gene functions in a step-wise process of protein degradation through the N-end rule pathway. This protein acts as a tertiary destabilizing enzyme that deamidates N-terminal L-Asn residues on proteins to produce N-terminal L-Asp. L-Asp substrates are subsequently conjugated to L-Arg, which is recognized by specific E3 ubiquitin ligases and targeted to the proteasome. Pseudogenes of this gene are located on the long arms of chromosomes 8, 10 and 12. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":15037853,"end":15056079,"strand":-1,"description":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]"}, {"versioned_ensembl_gene_id":"ENSG00000253625.1","gene_symbol":"IGKV2-23","gene_name":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28924","summary":null,"start":89172022,"end":89172553,"strand":-1,"description":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]"}, {"versioned_ensembl_gene_id":"ENSG00000223840.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30228173,"end":30232162,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000253578.1","gene_symbol":"IGKV1-22","gene_name":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28936","summary":null,"start":89170775,"end":89171212,"strand":-1,"description":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]"}, {"versioned_ensembl_gene_id":"ENSG00000167081.16","gene_symbol":"PBX3","gene_name":"PBX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:8634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5090","summary":null,"start":125747345,"end":125967377,"strand":1,"description":"PBX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:8634]"}, {"versioned_ensembl_gene_id":"ENSG00000163378.13","gene_symbol":"EOGT","gene_name":"EGF domain specific O-linked N-acetylglucosamine transferase [Source:HGNC Symbol;Acc:HGNC:28526]","synonyms":"FLJ33770,C3orf64,AER61","biotype":"protein_coding","ncbi_id":"285203","summary":"This gene encodes an enzyme that acts in the lumen of the endoplasmic reticulum to catalyze the transfer of N-acetylglucosamine to serine or threonine residues of extracellular-targeted proteins. This enzyme modifies proteins containing eukaryotic growth factor (EGF)-like domains, including the Notch receptor, thereby regulating developmental signalling. Mutations in this gene have been observed in individuals with Adams-Oliver syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":68975214,"end":69013961,"strand":-1,"description":"EGF domain specific O-linked N-acetylglucosamine transferase [Source:HGNC Symbol;Acc:HGNC:28526]"}, {"versioned_ensembl_gene_id":"ENSG00000139567.12","gene_symbol":"ACVRL1","gene_name":"activin A receptor like type 1 [Source:HGNC Symbol;Acc:HGNC:175]","synonyms":"ORW2,HHT2,HHT,ALK1,ACVRLK1","biotype":"protein_coding","ncbi_id":"94","summary":"This gene encodes a type I cell-surface receptor for the TGF-beta superfamily of ligands. It shares with other type I receptors a high degree of similarity in serine-threonine kinase subdomains, a glycine- and serine-rich region (called the GS domain) preceding the kinase domain, and a short C-terminal tail. The encoded protein, sometimes termed ALK1, shares similar domain structures with other closely related ALK or activin receptor-like kinase proteins that form a subfamily of receptor serine/threonine kinases. Mutations in this gene are associated with hemorrhagic telangiectasia type 2, also known as Rendu-Osler-Weber syndrome 2. [provided by RefSeq, Jul 2008]","start":51906908,"end":51923361,"strand":1,"description":"activin A receptor like type 1 [Source:HGNC Symbol;Acc:HGNC:175]"}, {"versioned_ensembl_gene_id":"ENSG00000214653.4","gene_symbol":"HNRNPA3P3","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643689","summary":null,"start":140032344,"end":140033480,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39772]"}, {"versioned_ensembl_gene_id":"ENSG00000164040.16","gene_symbol":"PGRMC2","gene_name":"progesterone receptor membrane component 2 [Source:HGNC Symbol;Acc:HGNC:16089]","synonyms":"PMBP,DG6","biotype":"protein_coding","ncbi_id":"10424","summary":null,"start":128269237,"end":128288829,"strand":-1,"description":"progesterone receptor membrane component 2 [Source:HGNC Symbol;Acc:HGNC:16089]"}, {"versioned_ensembl_gene_id":"ENSG00000238111.1","gene_symbol":"AC066692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23900693,"end":23901149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132698.14","gene_symbol":"RAB25","gene_name":"RAB25, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18238]","synonyms":"CATX-8","biotype":"protein_coding","ncbi_id":"57111","summary":"The protein encoded by this gene is a member of the RAS superfamily of small GTPases. The encoded protein is involved in membrane trafficking and cell survival. This gene has been found to be a tumor suppressor and an oncogene, depending on the context. Two variants, one protein-coding and the other not, have been found for this gene. [provided by RefSeq, Nov 2015]","start":156061160,"end":156070514,"strand":1,"description":"RAB25, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18238]"}, {"versioned_ensembl_gene_id":"ENSG00000211898.7","gene_symbol":"IGHD","gene_name":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]","synonyms":"MGC29633,FLJ46727,FLJ00382","biotype":"IG_C_gene","ncbi_id":"3495","summary":null,"start":105836765,"end":105845678,"strand":-1,"description":"immunoglobulin heavy constant delta [Source:HGNC Symbol;Acc:HGNC:5480]"}, {"versioned_ensembl_gene_id":"ENSG00000283959.1","gene_symbol":"AP002851.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":102656464,"end":102687118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206522.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29111883,"end":29112818,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000187720.14","gene_symbol":"THSD4","gene_name":"thrombospondin type 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25835]","synonyms":"ADAMTSL6,PRO34005,FVSY9334,FLJ13710","biotype":"protein_coding","ncbi_id":"79875","summary":null,"start":71096952,"end":71783383,"strand":1,"description":"thrombospondin type 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25835]"}, {"versioned_ensembl_gene_id":"ENSG00000254028.1","gene_symbol":"AC083843.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134832747,"end":134834482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073803.13","gene_symbol":"MAP3K13","gene_name":"mitogen-activated protein kinase kinase kinase 13 [Source:HGNC Symbol;Acc:HGNC:6852]","synonyms":"MEKK13,LZK","biotype":"protein_coding","ncbi_id":"9175","summary":"The protein encoded by this gene is a member of serine/threonine protein kinase family. This kinase contains a dual leucine-zipper motif, and has been shown to form dimers/oligomers through its leucine-zipper motif. This kinase can phosphorylate and activate MAPK8/JNK, MAP2K7/MKK7, which suggests a role in the JNK signaling pathway. [provided by RefSeq, Jul 2008]","start":185282941,"end":185489097,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 13 [Source:HGNC Symbol;Acc:HGNC:6852]"}, {"versioned_ensembl_gene_id":"ENSG00000157388.15","gene_symbol":"CACNA1D","gene_name":"calcium voltage-gated channel subunit alpha1 D [Source:HGNC Symbol;Acc:HGNC:1391]","synonyms":"CCHL1A2,Cav1.3,CACNL1A2,CACN4,CACH3","biotype":"protein_coding","ncbi_id":"776","summary":"Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, namely alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1D subunit. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":53328963,"end":53813733,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 D [Source:HGNC Symbol;Acc:HGNC:1391]"}, {"versioned_ensembl_gene_id":"ENSG00000254287.1","gene_symbol":"AC007991.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39918076,"end":39920890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000016391.10","gene_symbol":"CHDH","gene_name":"choline dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55349","summary":"The protein encoded by this gene is a choline dehydrogenase that localizes to the mitochondrion. Variations in this gene can affect susceptibility to choline deficiency. A few transcript variants have been found for this gene, but the full-length nature of only one has been characterized to date. [provided by RefSeq, Dec 2010]","start":53812335,"end":53846390,"strand":-1,"description":"choline dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24288]"}, {"versioned_ensembl_gene_id":"ENSG00000253364.2","gene_symbol":"AL928742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105647924,"end":105649057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231104.8","gene_symbol":"AC022395.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118017487,"end":118045810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279478.1","gene_symbol":"AC127071.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130383364,"end":130383890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124196.5","gene_symbol":"GTSF1L","gene_name":"gametocyte specific factor 1 like [Source:HGNC Symbol;Acc:HGNC:16198]","synonyms":"FAM112A,dJ1028D15.4,C20orf65","biotype":"protein_coding","ncbi_id":"149699","summary":null,"start":43726164,"end":43726998,"strand":-1,"description":"gametocyte specific factor 1 like [Source:HGNC Symbol;Acc:HGNC:16198]"}, {"versioned_ensembl_gene_id":"ENSG00000226795.1","gene_symbol":"AL929561.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076560,"end":29077155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254185.1","gene_symbol":"AC021001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109470131,"end":109471117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206525.2","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044198,"end":29045225,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000272777.1","gene_symbol":"AC019131.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99067256,"end":99068125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143450.16","gene_symbol":"OAZ3","gene_name":"ornithine decarboxylase antizyme 3 [Source:HGNC Symbol;Acc:HGNC:8097]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51686","summary":"The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamine levels. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 3, the third member of the antizyme family. Like antizymes 1 and 2, antizyme 3 inhibits ODC activity and polyamine uptake; however, it does not stimulate ODC degradation. Also, while antizymes 1 and 2 have broad tissue distribution, expression of antizyme 3 is restricted to haploid germ cells in testis, suggesting a distinct role for this antizyme in spermiogenesis. Antizyme 3 gene knockout studies showed that homozygous mutant male mice were infertile, and indicated the likely role of this antizyme in the formation of a rigid connection between the sperm head and tail during spermatogenesis. Alternatively spliced transcript variants encoding different isoforms, including one resulting from the use of non-AUG (CUG) translation initiation codon, have been found for this gene. [provided by RefSeq, Dec 2014]","start":151762899,"end":151771334,"strand":1,"description":"ornithine decarboxylase antizyme 3 [Source:HGNC Symbol;Acc:HGNC:8097]"}, {"versioned_ensembl_gene_id":"ENSG00000176101.11","gene_symbol":"SSNA1","gene_name":"SS nuclear autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11321]","synonyms":"NA14,N14","biotype":"protein_coding","ncbi_id":"8636","summary":null,"start":137188647,"end":137190370,"strand":1,"description":"SS nuclear autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11321]"}, {"versioned_ensembl_gene_id":"ENSG00000182173.12","gene_symbol":"TSEN54","gene_name":"tRNA splicing endonuclease subunit 54 [Source:HGNC Symbol;Acc:HGNC:27561]","synonyms":"SEN54L,SEN54","biotype":"protein_coding","ncbi_id":"283989","summary":"This gene encodes a subunit of the tRNA splicing endonuclease complex, which catalyzes the removal of introns from precursor tRNAs. The complex is also implicated in pre-mRNA 3-prime end processing. Mutations in this gene result in pontocerebellar hypoplasia type 2.[provided by RefSeq, Oct 2009]","start":75516060,"end":75524739,"strand":1,"description":"tRNA splicing endonuclease subunit 54 [Source:HGNC Symbol;Acc:HGNC:27561]"}, {"versioned_ensembl_gene_id":"ENSG00000188396.3","gene_symbol":"TCTEX1D4","gene_name":"Tctex1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343521","summary":null,"start":44805913,"end":44806675,"strand":-1,"description":"Tctex1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32315]"}, {"versioned_ensembl_gene_id":"ENSG00000259015.1","gene_symbol":"AL442663.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72960595,"end":72961993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137714.2","gene_symbol":"FDX1","gene_name":"ferredoxin 1 [Source:HGNC Symbol;Acc:HGNC:3638]","synonyms":"FDX,ADX","biotype":"protein_coding","ncbi_id":"2230","summary":"This gene encodes a small iron-sulfur protein that transfers electrons from NADPH through ferredoxin reductase to mitochondrial cytochrome P450, involved in steroid, vitamin D, and bile acid metabolism. Pseudogenes of this functional gene are found on chromosomes 20 and 21. [provided by RefSeq, Aug 2011]","start":110429883,"end":110464881,"strand":1,"description":"ferredoxin 1 [Source:HGNC Symbol;Acc:HGNC:3638]"}, {"versioned_ensembl_gene_id":"ENSG00000275944.1","gene_symbol":"AC244100.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36001419,"end":36011618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188833.9","gene_symbol":"ENTPD8","gene_name":"ectonucleoside triphosphate diphosphohydrolase 8 [Source:HGNC Symbol;Acc:HGNC:24860]","synonyms":"UNQ2492,NTPDase-8","biotype":"protein_coding","ncbi_id":"377841","summary":null,"start":137434364,"end":137441816,"strand":-1,"description":"ectonucleoside triphosphate diphosphohydrolase 8 [Source:HGNC Symbol;Acc:HGNC:24860]"}, {"versioned_ensembl_gene_id":"ENSG00000258210.1","gene_symbol":"AC144548.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110387463,"end":110445548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258861.1","gene_symbol":"MIR381HG","gene_name":"MIR381 host gene [Source:HGNC Symbol;Acc:HGNC:20136]","synonyms":"NCRNA00225,C14orf89","biotype":"lincRNA","ncbi_id":"378881","summary":null,"start":101045157,"end":101051795,"strand":1,"description":"MIR381 host gene [Source:HGNC Symbol;Acc:HGNC:20136]"}, {"versioned_ensembl_gene_id":"ENSG00000176239.7","gene_symbol":"OR51B6","gene_name":"olfactory receptor family 51 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:19600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390058","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5351508,"end":5352446,"strand":1,"description":"olfactory receptor family 51 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:19600]"}, {"versioned_ensembl_gene_id":"ENSG00000117479.12","gene_symbol":"SLC19A2","gene_name":"solute carrier family 19 member 2 [Source:HGNC Symbol;Acc:HGNC:10938]","synonyms":"TRMA,THTR1","biotype":"protein_coding","ncbi_id":"10560","summary":"This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":169463909,"end":169486003,"strand":-1,"description":"solute carrier family 19 member 2 [Source:HGNC Symbol;Acc:HGNC:10938]"}, {"versioned_ensembl_gene_id":"ENSG00000282048.1","gene_symbol":"AL591742.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":114032393,"end":114034511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265987.1","gene_symbol":"AC011933.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75344405,"end":75373662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253809.1","gene_symbol":"AL160262.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70222758,"end":70242156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236520.2","gene_symbol":"GPC6-AS1","gene_name":"GPC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39909]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873972","summary":null,"start":94154193,"end":94187991,"strand":-1,"description":"GPC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39909]"}, {"versioned_ensembl_gene_id":"ENSG00000260970.1","gene_symbol":"AC006288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119495375,"end":119524125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120322.3","gene_symbol":"PCDHB8","gene_name":"protocadherin beta 8 [Source:HGNC Symbol;Acc:HGNC:8693]","synonyms":"PCDH3I,PCDH-BETA8","biotype":"protein_coding","ncbi_id":"56128","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141177790,"end":141180529,"strand":1,"description":"protocadherin beta 8 [Source:HGNC Symbol;Acc:HGNC:8693]"}, {"versioned_ensembl_gene_id":"ENSG00000159023.19","gene_symbol":"EPB41","gene_name":"erythrocyte membrane protein band 4.1 [Source:HGNC Symbol;Acc:HGNC:3377]","synonyms":"EL1,4.1R","biotype":"protein_coding","ncbi_id":"2035","summary":"The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009]","start":28887091,"end":29120046,"strand":1,"description":"erythrocyte membrane protein band 4.1 [Source:HGNC Symbol;Acc:HGNC:3377]"}, {"versioned_ensembl_gene_id":"ENSG00000254897.1","gene_symbol":"AP003035.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85452282,"end":85453698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275152.4","gene_symbol":"CCL16","gene_name":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]","synonyms":"Mtn-1,LMC,LEC,LCC-1,HCC-4,CKb12,SCYL4,SCYA16,NCC-4","biotype":"protein_coding","ncbi_id":"6360","summary":"This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for lymphocytes and monocytes but not for neutrophils. This cytokine also shows a potent myelosuppressive activity and suppresses proliferation of myeloid progenitor cells. The expression of this gene is upregulated by IL-10. [provided by RefSeq, Jul 2008]","start":35976493,"end":35981496,"strand":-1,"description":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]"}, {"versioned_ensembl_gene_id":"ENSG00000069482.6","gene_symbol":"GAL","gene_name":"galanin and GMAP prepropeptide [Source:HGNC Symbol;Acc:HGNC:4114]","synonyms":"GMAP,GLNN,GALN,GAL-GMAP","biotype":"protein_coding","ncbi_id":"51083","summary":"This gene encodes a neuroendocrine peptide that is widely expressed in the central and peripheral nervous systems and also the gastrointestinal tract, pancreas, adrenal gland and urogenital tract. The encoded protein is a precursor that is proteolytically processed to generate two mature peptides: galanin and galanin message-associated peptide (GMAP). Galanin has diverse physiological functions including nociception, feeding and energy homeostasis, osmotic regulation and water balance. GMAP has been demonstrated to possess antifungal activity and hypothesized to be part of the innate immune system. [provided by RefSeq, Jul 2015]","start":68683779,"end":68691175,"strand":1,"description":"galanin and GMAP prepropeptide [Source:HGNC Symbol;Acc:HGNC:4114]"}, {"versioned_ensembl_gene_id":"ENSG00000227824.1","gene_symbol":"AC122136.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215869923,"end":215870518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270682.1","gene_symbol":"AP003357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97788210,"end":97788357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112280.15","gene_symbol":"COL9A1","gene_name":"collagen type IX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2217]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1297","summary":"This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":70215061,"end":70303083,"strand":-1,"description":"collagen type IX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2217]"}, {"versioned_ensembl_gene_id":"ENSG00000225764.1","gene_symbol":"P3H2-AS1","gene_name":"P3H2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40886]","synonyms":"LEPREL1-AS1","biotype":"antisense_RNA","ncbi_id":"101929152","summary":null,"start":190120964,"end":190144846,"strand":1,"description":"P3H2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40886]"}, {"versioned_ensembl_gene_id":"ENSG00000227845.2","gene_symbol":"AL627223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125372325,"end":125372766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257087.1","gene_symbol":"AP003174.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115538869,"end":115539384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112852.6","gene_symbol":"PCDHB2","gene_name":"protocadherin beta 2 [Source:HGNC Symbol;Acc:HGNC:8687]","synonyms":"PCDH-BETA2","biotype":"protein_coding","ncbi_id":"56133","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141094578,"end":141098703,"strand":1,"description":"protocadherin beta 2 [Source:HGNC Symbol;Acc:HGNC:8687]"}, {"versioned_ensembl_gene_id":"ENSG00000171815.5","gene_symbol":"PCDHB1","gene_name":"protocadherin beta 1 [Source:HGNC Symbol;Acc:HGNC:8680]","synonyms":"PCDH-BETA1","biotype":"protein_coding","ncbi_id":"29930","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141051135,"end":141059344,"strand":1,"description":"protocadherin beta 1 [Source:HGNC Symbol;Acc:HGNC:8680]"}, {"versioned_ensembl_gene_id":"ENSG00000110536.13","gene_symbol":"PTPMT1","gene_name":"protein tyrosine phosphatase, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:26965]","synonyms":"PLIP,MOSP,DUSP23","biotype":"protein_coding","ncbi_id":"114971","summary":null,"start":47565430,"end":47573461,"strand":1,"description":"protein tyrosine phosphatase, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:26965]"}, {"versioned_ensembl_gene_id":"ENSG00000162366.7","gene_symbol":"PDZK1IP1","gene_name":"PDZK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16887]","synonyms":"SPAP,MAP17,DD96","biotype":"protein_coding","ncbi_id":"10158","summary":null,"start":47183593,"end":47191044,"strand":-1,"description":"PDZK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16887]"}, {"versioned_ensembl_gene_id":"ENSG00000101162.3","gene_symbol":"TUBB1","gene_name":"tubulin beta 1 class VI [Source:HGNC Symbol;Acc:HGNC:16257]","synonyms":"dJ543J19.4","biotype":"protein_coding","ncbi_id":"81027","summary":"This gene encodes a member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is specifically expressed in platelets and megakaryocytes and may be involved in proplatelet production and platelet release. A mutations in this gene is associated with autosomal dominant macrothrombocytopenia. Two pseudogenes of this gene are found on chromosome Y.[provided by RefSeq, Jul 2010]","start":59019254,"end":59026654,"strand":1,"description":"tubulin beta 1 class VI [Source:HGNC Symbol;Acc:HGNC:16257]"}, {"versioned_ensembl_gene_id":"ENSG00000269095.1","gene_symbol":"AC010646.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17235940,"end":17255448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273806.1","gene_symbol":"AL137847.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83201957,"end":83202065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171345.13","gene_symbol":"KRT19","gene_name":"keratin 19 [Source:HGNC Symbol;Acc:HGNC:6436]","synonyms":"K1CS,K19,CK19,MGC15366","biotype":"protein_coding","ncbi_id":"3880","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. Unlike its related family members, this smallest known acidic cytokeratin is not paired with a basic cytokeratin in epithelial cells. It is specifically expressed in the periderm, the transiently superficial layer that envelopes the developing epidermis. The type I cytokeratins are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2008]","start":41523617,"end":41528308,"strand":-1,"description":"keratin 19 [Source:HGNC Symbol;Acc:HGNC:6436]"}, {"versioned_ensembl_gene_id":"ENSG00000149187.18","gene_symbol":"CELF1","gene_name":"CUGBP Elav-like family member 1 [Source:HGNC Symbol;Acc:HGNC:2549]","synonyms":"CUGBP,CUG-BP,BRUNOL2,NAPOR,NAB50,hNab50,EDEN-BP,CUGBP1","biotype":"protein_coding","ncbi_id":"10658","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":47465933,"end":47565569,"strand":-1,"description":"CUGBP Elav-like family member 1 [Source:HGNC Symbol;Acc:HGNC:2549]"}, {"versioned_ensembl_gene_id":"ENSG00000038219.12","gene_symbol":"BOD1L1","gene_name":"biorientation of chromosomes in cell division 1 like 1 [Source:HGNC Symbol;Acc:HGNC:31792]","synonyms":"KIAA1327,FLJ33215,FAM44A,BOD1L","biotype":"protein_coding","ncbi_id":"259282","summary":null,"start":13568738,"end":13627723,"strand":-1,"description":"biorientation of chromosomes in cell division 1 like 1 [Source:HGNC Symbol;Acc:HGNC:31792]"}, {"versioned_ensembl_gene_id":"ENSG00000231023.6","gene_symbol":"LINC00326","gene_name":"long intergenic non-protein coding RNA 326 [Source:HGNC Symbol;Acc:HGNC:41926]","synonyms":"NCRNA00326","biotype":"lincRNA","ncbi_id":"285735","summary":null,"start":133088080,"end":133106578,"strand":1,"description":"long intergenic non-protein coding RNA 326 [Source:HGNC Symbol;Acc:HGNC:41926]"}, {"versioned_ensembl_gene_id":"ENSG00000278941.1","gene_symbol":"SMG6-IT1","gene_name":"SMG6 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1220]","synonyms":"C17orf6","biotype":"TEC","ncbi_id":"53400","summary":null,"start":2235713,"end":2236086,"strand":-1,"description":"SMG6 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:1220]"}, {"versioned_ensembl_gene_id":"ENSG00000236554.1","gene_symbol":"ASNSP3","gene_name":"asparagine synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39399]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100423061","summary":null,"start":100062296,"end":100063601,"strand":-1,"description":"asparagine synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39399]"}, {"versioned_ensembl_gene_id":"ENSG00000022355.16","gene_symbol":"GABRA1","gene_name":"gamma-aminobutyric acid type A receptor alpha1 subunit [Source:HGNC Symbol;Acc:HGNC:4075]","synonyms":"EJM5","biotype":"protein_coding","ncbi_id":"2554","summary":"This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4. Multiple transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":161847063,"end":161899981,"strand":1,"description":"gamma-aminobutyric acid type A receptor alpha1 subunit [Source:HGNC Symbol;Acc:HGNC:4075]"}, {"versioned_ensembl_gene_id":"ENSG00000229990.3","gene_symbol":"AC022400.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73841833,"end":73847115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256315.1","gene_symbol":"AP000462.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":115396756,"end":115397658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273373.1","gene_symbol":"AL355488.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110370154,"end":110373003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204011.4","gene_symbol":"COL5A1-AS1","gene_name":"COL5A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31368]","synonyms":"C9orf104,bA54A22.4","biotype":"antisense_RNA","ncbi_id":"414316","summary":null,"start":134649385,"end":134652843,"strand":-1,"description":"COL5A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31368]"}, {"versioned_ensembl_gene_id":"ENSG00000255210.1","gene_symbol":"AP001889.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110049528,"end":110050160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136104.19","gene_symbol":"RNASEH2B","gene_name":"ribonuclease H2 subunit B [Source:HGNC Symbol;Acc:HGNC:25671]","synonyms":"FLJ11712,DLEU8,AGS2","biotype":"protein_coding","ncbi_id":"79621","summary":"RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]","start":50909678,"end":50973745,"strand":1,"description":"ribonuclease H2 subunit B [Source:HGNC Symbol;Acc:HGNC:25671]"}, {"versioned_ensembl_gene_id":"ENSG00000224776.3","gene_symbol":"RPSAP50","gene_name":"ribosomal protein SA pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35896]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644109","summary":null,"start":109982192,"end":109983043,"strand":1,"description":"ribosomal protein SA pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35896]"}, {"versioned_ensembl_gene_id":"ENSG00000197079.8","gene_symbol":"KRT35","gene_name":"keratin 35 [Source:HGNC Symbol;Acc:HGNC:6453]","synonyms":"KRTHA5,Ha-5","biotype":"protein_coding","ncbi_id":"3886","summary":"The protein encoded by this gene is a member of the keratin gene family. This type I hair keratin is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41476689,"end":41481140,"strand":-1,"description":"keratin 35 [Source:HGNC Symbol;Acc:HGNC:6453]"}, {"versioned_ensembl_gene_id":"ENSG00000243572.1","gene_symbol":"LINC02017","gene_name":"long intergenic non-protein coding RNA 2017 [Source:HGNC Symbol;Acc:HGNC:52852]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377096","summary":null,"start":55178172,"end":55189214,"strand":1,"description":"long intergenic non-protein coding RNA 2017 [Source:HGNC Symbol;Acc:HGNC:52852]"}, {"versioned_ensembl_gene_id":"ENSG00000119703.13","gene_symbol":"ZC2HC1C","gene_name":"zinc finger C2HC-type containing 1C [Source:HGNC Symbol;Acc:HGNC:20354]","synonyms":"FAM164C,C14orf140","biotype":"protein_coding","ncbi_id":"79696","summary":null,"start":75064170,"end":75079987,"strand":1,"description":"zinc finger C2HC-type containing 1C [Source:HGNC Symbol;Acc:HGNC:20354]"}, {"versioned_ensembl_gene_id":"ENSG00000212864.3","gene_symbol":"RNF208","gene_name":"ring finger protein 208 [Source:HGNC Symbol;Acc:HGNC:25420]","synonyms":"DKFZP761H1710","biotype":"protein_coding","ncbi_id":"727800","summary":null,"start":137220247,"end":137221581,"strand":-1,"description":"ring finger protein 208 [Source:HGNC Symbol;Acc:HGNC:25420]"}, {"versioned_ensembl_gene_id":"ENSG00000258978.1","gene_symbol":"HIF1AP1","gene_name":"hypoxia inducible factor 1 alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874523","summary":null,"start":75116426,"end":75116600,"strand":-1,"description":"hypoxia inducible factor 1 alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43016]"}, {"versioned_ensembl_gene_id":"ENSG00000174437.16","gene_symbol":"ATP2A2","gene_name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:812]","synonyms":"SERCA2,DAR,ATP2B","biotype":"protein_coding","ncbi_id":"488","summary":"This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of the skeletal muscle. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Other types of mutations in this gene have been associated with various forms of muscular dystrophies. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2019]","start":110280756,"end":110351093,"strand":1,"description":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:812]"}, {"versioned_ensembl_gene_id":"ENSG00000118508.4","gene_symbol":"RAB32","gene_name":"RAB32, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10981","summary":"The protein encoded by this gene anchors the type II regulatory subunit of protein kinase A to the mitochondrion and aids in mitochondrial fission. The encoded protein also appears to be involved in autophagy and melanosome secretion. Variations in this gene may be linked to leprosy. [provided by RefSeq, Dec 2015]","start":146543693,"end":146554965,"strand":1,"description":"RAB32, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9772]"}, {"versioned_ensembl_gene_id":"ENSG00000176742.2","gene_symbol":"OR51V1","gene_name":"olfactory receptor family 51 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:19597]","synonyms":"OR51A12","biotype":"protein_coding","ncbi_id":"283111","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5199735,"end":5200700,"strand":-1,"description":"olfactory receptor family 51 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:19597]"}, {"versioned_ensembl_gene_id":"ENSG00000166004.14","gene_symbol":"CEP295","gene_name":"centrosomal protein 295 [Source:HGNC Symbol;Acc:HGNC:29366]","synonyms":"KIAA1731","biotype":"protein_coding","ncbi_id":"85459","summary":null,"start":93661639,"end":93730358,"strand":1,"description":"centrosomal protein 295 [Source:HGNC Symbol;Acc:HGNC:29366]"}, {"versioned_ensembl_gene_id":"ENSG00000228199.1","gene_symbol":"AL845450.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30176697,"end":30178517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138246.15","gene_symbol":"DNAJC13","gene_name":"DnaJ heat shock protein family (Hsp40) member C13 [Source:HGNC Symbol;Acc:HGNC:30343]","synonyms":"RME8,KIAA0678","biotype":"protein_coding","ncbi_id":"23317","summary":"This gene encodes a member of the Dnaj protein family whose members act as co-chaperones of a partner heat-shock protein by binding to the latter and stimulating ATP hydrolysis. The encoded protein associates with the heat-shock protein Hsc70 and plays a role in clathrin-mediated endocytosis. It may also be involved in post-endocytic transport mechanisms via its associations with other proteins, including the sorting nexin SNX1. Mutations in this gene are associated with Parkinson's disease. [provided by RefSeq, Jun 2016]","start":132417526,"end":132539032,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C13 [Source:HGNC Symbol;Acc:HGNC:30343]"}, {"versioned_ensembl_gene_id":"ENSG00000273969.1","gene_symbol":"AC138747.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28484946,"end":28485066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235887.2","gene_symbol":"AC239859.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143499187,"end":143500512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104951.15","gene_symbol":"IL4I1","gene_name":"interleukin 4 induced 1 [Source:HGNC Symbol;Acc:HGNC:19094]","synonyms":"FIG1","biotype":"protein_coding","ncbi_id":"259307","summary":"This gene encodes a secreted L-amino acid oxidase protein which primarily catabolizes L-phenylalanine and, to a lesser extent, L-arginine. The expression of this gene is induced by the cytokine interleukin 4 in B cells. This gene is also expressed in macrophages and dendritic cells. This protein may play a role immune system escape as it is expressed in tumor-associated macrophages and suppresses T-cell responses. This protein also contains domains thought to be involved in the binding of flavin adenine dinucleotide (FAD) cofactor. Multiple transcript variants encoding different isoforms have been found for this gene. Some transcripts of this gene share a promoter and exons of the 5' UTR with the overlapping NUP62 gene. [provided by RefSeq, Jul 2020]","start":49889654,"end":49929539,"strand":-1,"description":"interleukin 4 induced 1 [Source:HGNC Symbol;Acc:HGNC:19094]"}, {"versioned_ensembl_gene_id":"ENSG00000232508.1","gene_symbol":"MRPL45P1","gene_name":"mitochondrial ribosomal protein L45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359747","summary":null,"start":88364695,"end":88365608,"strand":-1,"description":"mitochondrial ribosomal protein L45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29715]"}, {"versioned_ensembl_gene_id":"ENSG00000282587.1","gene_symbol":"AC138747.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28455755,"end":28455878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095209.11","gene_symbol":"TMEM38B","gene_name":"transmembrane protein 38B [Source:HGNC Symbol;Acc:HGNC:25535]","synonyms":"TRIC-B,FLJ10493,D4Ertd89e,C9orf87,bA219P18.1","biotype":"protein_coding","ncbi_id":"55151","summary":"This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]","start":105694544,"end":105776612,"strand":1,"description":"transmembrane protein 38B [Source:HGNC Symbol;Acc:HGNC:25535]"}, {"versioned_ensembl_gene_id":"ENSG00000233025.1","gene_symbol":"CRYZP1","gene_name":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1430","summary":null,"start":103088664,"end":103089610,"strand":-1,"description":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]"}, {"versioned_ensembl_gene_id":"ENSG00000100281.13","gene_symbol":"HMGXB4","gene_name":"HMG-box containing 4 [Source:HGNC Symbol;Acc:HGNC:5003]","synonyms":"THC211630,HMG2L1","biotype":"protein_coding","ncbi_id":"10042","summary":"High mobility group (HMG) proteins are nonhistone chromosomal proteins. See HMG2 (MIM 163906) for additional information on HMG proteins.[supplied by OMIM, Nov 2010]","start":35257452,"end":35295807,"strand":1,"description":"HMG-box containing 4 [Source:HGNC Symbol;Acc:HGNC:5003]"}, {"versioned_ensembl_gene_id":"ENSG00000249068.1","gene_symbol":"AC008417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109840128,"end":109840692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261556.9","gene_symbol":"SMG1P7","gene_name":"SMG1P7, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49864]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100506060","summary":null,"start":70219574,"end":70246610,"strand":-1,"description":"SMG1P7, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49864]"}, {"versioned_ensembl_gene_id":"ENSG00000213024.11","gene_symbol":"NUP62","gene_name":"nucleoporin 62 [Source:HGNC Symbol;Acc:HGNC:8066]","synonyms":"SNDI,p62,MGC841,IBSN,FLJ43869,FLJ20822,DKFZp547L134","biotype":"protein_coding","ncbi_id":"23636","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of the FG-repeat containing nucleoporins and is localized to the nuclear pore central plug. This protein associates with the importin alpha/beta complex which is involved in the import of proteins containing nuclear localization signals. Multiple transcript variants of this gene encode a single protein isoform. [provided by RefSeq, Jul 2008]","start":49906825,"end":49929763,"strand":-1,"description":"nucleoporin 62 [Source:HGNC Symbol;Acc:HGNC:8066]"}, {"versioned_ensembl_gene_id":"ENSG00000228002.2","gene_symbol":"DHX9P1","gene_name":"DEAH-box helicase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2751]","synonyms":"DHX9P,DDX9P","biotype":"processed_pseudogene","ncbi_id":"1661","summary":null,"start":76984868,"end":76987943,"strand":1,"description":"DEAH-box helicase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2751]"}, {"versioned_ensembl_gene_id":"ENSG00000140470.13","gene_symbol":"ADAMTS17","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 17 [Source:HGNC Symbol;Acc:HGNC:17109]","synonyms":"FLJ32769,FLJ16363","biotype":"protein_coding","ncbi_id":"170691","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016]","start":99971589,"end":100342005,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 17 [Source:HGNC Symbol;Acc:HGNC:17109]"}, {"versioned_ensembl_gene_id":"ENSG00000257995.1","gene_symbol":"AC084365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90617759,"end":90622822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273323.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"dJ207F6.1,NOL5BP,NOL5B,NOP56-L","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783631,"end":28784002,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000170632.13","gene_symbol":"ARMC10","gene_name":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]","synonyms":"MGC3195,SVH","biotype":"protein_coding","ncbi_id":"83787","summary":"This gene encodes a protein that contains an armadillo repeat and transmembrane domain. The encoded protein decreases the transcriptional activity of the tumor suppressor protein p53 through direct interaction with the DNA-binding domain of p53, and may play a role in cell growth and survival. Upregulation of this gene may play a role in hepatocellular carcinoma. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Sep 2011]","start":103074881,"end":103099764,"strand":1,"description":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]"}, {"versioned_ensembl_gene_id":"ENSG00000154144.12","gene_symbol":"TBRG1","gene_name":"transforming growth factor beta regulator 1 [Source:HGNC Symbol;Acc:HGNC:29551]","synonyms":"TB-5,NIAM,FLJ14621","biotype":"protein_coding","ncbi_id":"84897","summary":null,"start":124622836,"end":124635398,"strand":1,"description":"transforming growth factor beta regulator 1 [Source:HGNC Symbol;Acc:HGNC:29551]"}, {"versioned_ensembl_gene_id":"ENSG00000251437.1","gene_symbol":"NDUFS5P4","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44042]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287817","summary":null,"start":98976800,"end":98977117,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44042]"}, {"versioned_ensembl_gene_id":"ENSG00000251367.1","gene_symbol":"AC091917.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109467353,"end":109467952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273068.1","gene_symbol":"Z99755.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35122661,"end":35127419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231090.1","gene_symbol":"MIR4422HG","gene_name":"MIR4422 host gene [Source:HGNC Symbol;Acc:HGNC:53113]","synonyms":"RP11-101C11.1","biotype":"lincRNA","ncbi_id":"109729135","summary":null,"start":55217861,"end":55234177,"strand":1,"description":"MIR4422 host gene [Source:HGNC Symbol;Acc:HGNC:53113]"}, {"versioned_ensembl_gene_id":"ENSG00000231095.1","gene_symbol":"GYG1P3","gene_name":"glycogenin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645506","summary":null,"start":55222379,"end":55223372,"strand":1,"description":"glycogenin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39711]"}, {"versioned_ensembl_gene_id":"ENSG00000238153.1","gene_symbol":"Z99755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35164304,"end":35165347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233080.3","gene_symbol":"LINC01399","gene_name":"long intergenic non-protein coding RNA 1399 [Source:HGNC Symbol;Acc:HGNC:50680]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"104310353","summary":null,"start":35119824,"end":35231056,"strand":-1,"description":"long intergenic non-protein coding RNA 1399 [Source:HGNC Symbol;Acc:HGNC:50680]"}, {"versioned_ensembl_gene_id":"ENSG00000251454.1","gene_symbol":"AC025244.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75341279,"end":75359024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272745.1","gene_symbol":"AC004948.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7619872,"end":7620543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163624.5","gene_symbol":"CDS1","gene_name":"CDP-diacylglycerol synthase 1 [Source:HGNC Symbol;Acc:HGNC:1800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1040","summary":"Breakdown products of phosphoinositides are ubiquitous second messengers that function downstream of many G protein-coupled receptors and tyrosine kinases regulating cell growth, calcium metabolism, and protein kinase C activity. This gene encodes an enzyme which regulates the amount of phosphatidylinositol available for signaling by catalyzing the conversion of phosphatidic acid to CDP-diacylglycerol. This enzyme is an integral membrane protein localized to two subcellular domains, the matrix side of the inner mitochondrial membrane where it is thought to be involved in the synthesis of phosphatidylglycerol and cardiolipin and the cytoplasmic side of the endoplasmic reticulum where it functions in phosphatidylinositol biosynthesis. Two genes encoding this enzyme have been identified in humans, one mapping to human chromosome 4q21 and a second to 20p13. [provided by RefSeq, Jul 2008]","start":84582979,"end":84651338,"strand":1,"description":"CDP-diacylglycerol synthase 1 [Source:HGNC Symbol;Acc:HGNC:1800]"}, {"versioned_ensembl_gene_id":"ENSG00000011677.12","gene_symbol":"GABRA3","gene_name":"gamma-aminobutyric acid type A receptor alpha3 subunit [Source:HGNC Symbol;Acc:HGNC:4077]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2556","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. [provided by RefSeq, Jul 2008]","start":152166234,"end":152451358,"strand":-1,"description":"gamma-aminobutyric acid type A receptor alpha3 subunit [Source:HGNC Symbol;Acc:HGNC:4077]"}, {"versioned_ensembl_gene_id":"ENSG00000142945.12","gene_symbol":"KIF2C","gene_name":"kinesin family member 2C [Source:HGNC Symbol;Acc:HGNC:6393]","synonyms":"KNSL6,CT139,MCAK","biotype":"protein_coding","ncbi_id":"11004","summary":"This gene encodes a kinesin-like protein that functions as a microtubule-dependent molecular motor. The encoded protein can depolymerize microtubules at the plus end, thereby promoting mitotic chromosome segregation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":44739818,"end":44767767,"strand":1,"description":"kinesin family member 2C [Source:HGNC Symbol;Acc:HGNC:6393]"}, {"versioned_ensembl_gene_id":"ENSG00000228430.9","gene_symbol":"AL162726.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":81977614,"end":82780194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237316.1","gene_symbol":"Z82196.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34711908,"end":34724919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276423.6","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54802859,"end":54817155,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000261793.1","gene_symbol":"AL929554.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":137168854,"end":137171984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170054.14","gene_symbol":"SERPINA9","gene_name":"serpin family A member 9 [Source:HGNC Symbol;Acc:HGNC:15995]","synonyms":"SERPINA11b,GCET1,CENTERIN","biotype":"protein_coding","ncbi_id":"327657","summary":null,"start":94462717,"end":94479689,"strand":-1,"description":"serpin family A member 9 [Source:HGNC Symbol;Acc:HGNC:15995]"}, {"versioned_ensembl_gene_id":"ENSG00000104973.16","gene_symbol":"MED25","gene_name":"mediator complex subunit 25 [Source:HGNC Symbol;Acc:HGNC:28845]","synonyms":"TCBAP0758,DKFZp434K0512,ARC92,ACID1","biotype":"protein_coding","ncbi_id":"81857","summary":"This gene encodes a component of the transcriptional coactivator complex termed the Mediator complex. This complex is required for transcription of most RNA polymerase II-dependent genes. The encoded protein plays a role in chromatin modification and in preinitiation complex assembly. Mutations in this gene are associated with Charcot-Marie-Tooth disease type 2B2. [provided by RefSeq, Apr 2010]","start":49818279,"end":49838816,"strand":1,"description":"mediator complex subunit 25 [Source:HGNC Symbol;Acc:HGNC:28845]"}, {"versioned_ensembl_gene_id":"ENSG00000240808.1","gene_symbol":"AC126389.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17137976,"end":17138265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272046.1","gene_symbol":"AL445647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87807634,"end":87811232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249917.2","gene_symbol":"LINC00536","gene_name":"long intergenic non-protein coding RNA 536 [Source:HGNC Symbol;Acc:HGNC:43645]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100859921","summary":null,"start":115950511,"end":116325059,"strand":-1,"description":"long intergenic non-protein coding RNA 536 [Source:HGNC Symbol;Acc:HGNC:43645]"}, {"versioned_ensembl_gene_id":"ENSG00000255921.1","gene_symbol":"AC026310.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24949163,"end":24960158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164077.13","gene_symbol":"MON1A","gene_name":"MON1 homolog A, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:28207]","synonyms":"SAND1,MGC13272","biotype":"protein_coding","ncbi_id":"84315","summary":null,"start":49908862,"end":49930173,"strand":-1,"description":"MON1 homolog A, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:28207]"}, {"versioned_ensembl_gene_id":"ENSG00000255028.5","gene_symbol":"AP003049.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109355085,"end":109583907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172818.9","gene_symbol":"OVOL1","gene_name":"ovo like transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:8525]","synonyms":"HOVO1","biotype":"protein_coding","ncbi_id":"5017","summary":"This gene encodes a putative zinc finger containing transcription factor that is highly similar to homologous protein in Drosophila and mouse. Based on known functions in these species, this protein is likely involved in hair formation and spermatogenesis in human as well. [provided by RefSeq, Aug 2011]","start":65787022,"end":65797219,"strand":1,"description":"ovo like transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:8525]"}, {"versioned_ensembl_gene_id":"ENSG00000221923.8","gene_symbol":"ZNF880","gene_name":"zinc finger protein 880 [Source:HGNC Symbol;Acc:HGNC:37249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400713","summary":null,"start":52369917,"end":52385795,"strand":1,"description":"zinc finger protein 880 [Source:HGNC Symbol;Acc:HGNC:37249]"}, {"versioned_ensembl_gene_id":"ENSG00000226275.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31648357,"end":31650629,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000214659.4","gene_symbol":"KRT8P26","gene_name":"keratin 8 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390211","summary":null,"start":65726939,"end":65728214,"strand":1,"description":"keratin 8 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33378]"}, {"versioned_ensembl_gene_id":"ENSG00000228923.1","gene_symbol":"AP000355.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24516508,"end":24518386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140932.9","gene_symbol":"CMTM2","gene_name":"CKLF like MARVEL transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19173]","synonyms":"MGC39436,FLJ25732,CKLFSF2","biotype":"protein_coding","ncbi_id":"146225","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that links the chemokine and the transmembrane 4 superfamilies of signaling molecules. The protein encoded by this gene may play an important role in testicular development. [provided by RefSeq, Jul 2008]","start":66579448,"end":66588275,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19173]"}, {"versioned_ensembl_gene_id":"ENSG00000198443.6","gene_symbol":"KRTAP4-1","gene_name":"keratin associated protein 4-1 [Source:HGNC Symbol;Acc:HGNC:18907]","synonyms":"KRTAP4-10,KAP4.10,KAP4.1","biotype":"protein_coding","ncbi_id":"85285","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41184102,"end":41185342,"strand":-1,"description":"keratin associated protein 4-1 [Source:HGNC Symbol;Acc:HGNC:18907]"}, {"versioned_ensembl_gene_id":"ENSG00000075415.12","gene_symbol":"SLC25A3","gene_name":"solute carrier family 25 member 3 [Source:HGNC Symbol;Acc:HGNC:10989]","synonyms":"PHC","biotype":"protein_coding","ncbi_id":"5250","summary":"The protein encoded by this gene catalyzes the transport of phosphate into the mitochondrial matrix, either by proton cotransport or in exchange for hydroxyl ions. The protein contains three related segments arranged in tandem which are related to those found in other characterized members of the mitochondrial carrier family. Both the N-terminal and C-terminal regions of this protein protrude toward the cytosol. Multiple alternatively spliced transcript variants have been isolated. [provided by RefSeq, Jul 2008]","start":98593591,"end":98606379,"strand":1,"description":"solute carrier family 25 member 3 [Source:HGNC Symbol;Acc:HGNC:10989]"}, {"versioned_ensembl_gene_id":"ENSG00000198464.13","gene_symbol":"ZNF480","gene_name":"zinc finger protein 480 [Source:HGNC Symbol;Acc:HGNC:23305]","synonyms":"MGC32104","biotype":"protein_coding","ncbi_id":"147657","summary":null,"start":52297177,"end":52325922,"strand":1,"description":"zinc finger protein 480 [Source:HGNC Symbol;Acc:HGNC:23305]"}, {"versioned_ensembl_gene_id":"ENSG00000234749.5","gene_symbol":"FAM90A21P","gene_name":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"619418","summary":null,"start":7564350,"end":7567360,"strand":-1,"description":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]"}, {"versioned_ensembl_gene_id":"ENSG00000212722.7","gene_symbol":"KRTAP4-9","gene_name":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]","synonyms":"KAP4.9","biotype":"protein_coding","ncbi_id":"100132386","summary":null,"start":41105332,"end":41106488,"strand":1,"description":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]"}, {"versioned_ensembl_gene_id":"ENSG00000273858.1","gene_symbol":"AC140113.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11042722,"end":11042943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277576.1","gene_symbol":"AC110741.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":133946677,"end":133947335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237943.6","gene_symbol":"PRKCQ-AS1","gene_name":"PRKCQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44689]","synonyms":"ENST00000414894.1","biotype":"processed_transcript","ncbi_id":"439949","summary":null,"start":6580419,"end":6616452,"strand":1,"description":"PRKCQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44689]"}, {"versioned_ensembl_gene_id":"ENSG00000064692.18","gene_symbol":"SNCAIP","gene_name":"synuclein alpha interacting protein [Source:HGNC Symbol;Acc:HGNC:11139]","synonyms":"SYPH1","biotype":"protein_coding","ncbi_id":"9627","summary":"This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":122311354,"end":122464219,"strand":1,"description":"synuclein alpha interacting protein [Source:HGNC Symbol;Acc:HGNC:11139]"}, {"versioned_ensembl_gene_id":"ENSG00000229408.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457659,"end":29464806,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000236660.6","gene_symbol":"FAM90A7P","gene_name":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]","synonyms":"FAM90A7","biotype":"unprocessed_pseudogene","ncbi_id":"441317","summary":"FAM90A7 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7556700,"end":7559712,"strand":-1,"description":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]"}, {"versioned_ensembl_gene_id":"ENSG00000273572.4","gene_symbol":"CDHR5","gene_name":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]","synonyms":"MUCDHL,MU-PCDH,FLJ20219,MUPCDH","biotype":"protein_coding","ncbi_id":"53841","summary":"This gene is a novel mucin-like gene that is a member of the cadherin superfamily. While encoding nonpolymorphic tandem repeats rich in proline, serine and threonine similar to mucin proteins, the gene also contains sequence encoding calcium-binding motifs found in all cadherins. The role of the hybrid extracellular region and the specific function of this protein have not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jan 2010]","start":616823,"end":626336,"strand":-1,"description":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]"}, {"versioned_ensembl_gene_id":"ENSG00000243746.1","gene_symbol":"EEF1A1P10","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3205]","synonyms":"EEF1AL8","biotype":"processed_pseudogene","ncbi_id":"100421829","summary":null,"start":144647186,"end":144648575,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3205]"}, {"versioned_ensembl_gene_id":"ENSG00000141258.12","gene_symbol":"SGSM2","gene_name":"small G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29026]","synonyms":"RUTBC1,KIAA0397","biotype":"protein_coding","ncbi_id":"9905","summary":"The protein encoded by this gene is a GTPase activator with activity towards RAB32 and RAB33B, which are regulators of membrane trafficking. The encoded protein inactivates RAB32 and can bind RAB9A-GTP, a protein required for RAB32 activation. [provided by RefSeq, Oct 2016]","start":2337498,"end":2381058,"strand":1,"description":"small G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29026]"}, {"versioned_ensembl_gene_id":"ENSG00000168785.7","gene_symbol":"TSPAN5","gene_name":"tetraspanin 5 [Source:HGNC Symbol;Acc:HGNC:17753]","synonyms":"Tspan-5,TM4SF9,NET-4","biotype":"protein_coding","ncbi_id":"10098","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. [provided by RefSeq, Jul 2008]","start":98470367,"end":98658629,"strand":-1,"description":"tetraspanin 5 [Source:HGNC Symbol;Acc:HGNC:17753]"}, {"versioned_ensembl_gene_id":"ENSG00000251523.1","gene_symbol":"AC108159.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98496364,"end":98509935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114786.16","gene_symbol":"ABHD14A-ACY1","gene_name":"ABHD14A-ACY1 readthrough [Source:HGNC Symbol;Acc:HGNC:38856]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526760","summary":"This locus represents naturally occurring read-through transcription between the neighboring abhydrolase domain containing 14A (ABHD14A) and aminoacylase 1 (ACY1) genes on chromosome 3. The read-through transcript encodes a protein that shares sequence identity with the downstream gene product but its N-terminal region is distinct due to the use of an alternate start codon relative to the upstream gene. [provided by RefSeq, Oct 2015]","start":51974706,"end":51989183,"strand":1,"description":"ABHD14A-ACY1 readthrough [Source:HGNC Symbol;Acc:HGNC:38856]"}, {"versioned_ensembl_gene_id":"ENSG00000115593.14","gene_symbol":"SMYD1","gene_name":"SET and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20986]","synonyms":"BOP,ZMYND22,KMT3D","biotype":"protein_coding","ncbi_id":"150572","summary":null,"start":88067780,"end":88113387,"strand":1,"description":"SET and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20986]"}, {"versioned_ensembl_gene_id":"ENSG00000230071.2","gene_symbol":"RPL4P6","gene_name":"ribosomal protein L4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271033","summary":null,"start":40586700,"end":40588003,"strand":-1,"description":"ribosomal protein L4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35611]"}, {"versioned_ensembl_gene_id":"ENSG00000283211.1","gene_symbol":"AL773545.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40167392,"end":40171329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258399.7","gene_symbol":"AL117190.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100836269,"end":100947194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249921.2","gene_symbol":"AC034207.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108784098,"end":108785552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258663.1","gene_symbol":"AL117190.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100834432,"end":100861026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176723.9","gene_symbol":"ZNF843","gene_name":"zinc finger protein 843 [Source:HGNC Symbol;Acc:HGNC:28710]","synonyms":"MGC46336","biotype":"protein_coding","ncbi_id":"283933","summary":null,"start":31432593,"end":31443160,"strand":-1,"description":"zinc finger protein 843 [Source:HGNC Symbol;Acc:HGNC:28710]"}, {"versioned_ensembl_gene_id":"ENSG00000242120.3","gene_symbol":"MDFIC2","gene_name":"MyoD family inhibitor domain containing 2 [Source:HGNC Symbol;Acc:HGNC:53442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"107986096","summary":null,"start":70196894,"end":70312726,"strand":-1,"description":"MyoD family inhibitor domain containing 2 [Source:HGNC Symbol;Acc:HGNC:53442]"}, {"versioned_ensembl_gene_id":"ENSG00000151422.12","gene_symbol":"FER","gene_name":"FER tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3655]","synonyms":"TYK3,PPP1R74","biotype":"protein_coding","ncbi_id":"2241","summary":"The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane receptor tyrosine kinases. It regulates cell-cell adhesion and mediates signaling from the cell surface to the cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Apr 2015]","start":108747822,"end":109196841,"strand":1,"description":"FER tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3655]"}, {"versioned_ensembl_gene_id":"ENSG00000250050.1","gene_symbol":"MTND4P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42226]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873193","summary":null,"start":25718082,"end":25719745,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42226]"}, {"versioned_ensembl_gene_id":"ENSG00000183060.15","gene_symbol":"LYSMD4","gene_name":"LysM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26571]","synonyms":"FLJ33008","biotype":"protein_coding","ncbi_id":"145748","summary":null,"start":99715697,"end":99733561,"strand":-1,"description":"LysM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26571]"}, {"versioned_ensembl_gene_id":"ENSG00000132646.10","gene_symbol":"PCNA","gene_name":"proliferating cell nuclear antigen [Source:HGNC Symbol;Acc:HGNC:8729]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5111","summary":"The protein encoded by this gene is found in the nucleus and is a cofactor of DNA polymerase delta. The encoded protein acts as a homotrimer and helps increase the processivity of leading strand synthesis during DNA replication. In response to DNA damage, this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway. Two transcript variants encoding the same protein have been found for this gene. Pseudogenes of this gene have been described on chromosome 4 and on the X chromosome. [provided by RefSeq, Jul 2008]","start":5114953,"end":5126626,"strand":-1,"description":"proliferating cell nuclear antigen [Source:HGNC Symbol;Acc:HGNC:8729]"}, {"versioned_ensembl_gene_id":"ENSG00000249277.1","gene_symbol":"AC092436.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25686202,"end":25686458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249959.5","gene_symbol":"AC024587.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107699835,"end":107716841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070366.13","gene_symbol":"SMG6","gene_name":"SMG6, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:17809]","synonyms":"SMG-6,KIAA0732,EST1A,C17orf31","biotype":"protein_coding","ncbi_id":"23293","summary":"This gene encodes a component of the telomerase ribonucleoprotein complex responsible for the replication and maintenance of chromosome ends. The encoded protein also plays a role in the nonsense-mediated mRNA decay (NMD) pathway, providing the endonuclease activity near the premature translation termination codon that is needed to initiate NMD. Alternatively spliced transcript variants encoding distinct protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":2059839,"end":2303771,"strand":-1,"description":"SMG6, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:17809]"}, {"versioned_ensembl_gene_id":"ENSG00000221852.4","gene_symbol":"KRTAP1-5","gene_name":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]","synonyms":"KAP1.5","biotype":"protein_coding","ncbi_id":"83895","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41026026,"end":41027202,"strand":-1,"description":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]"}, {"versioned_ensembl_gene_id":"ENSG00000108298.9","gene_symbol":"RPL19","gene_name":"ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:10312]","synonyms":"MGC71997,L19,FLJ27452,DKFZp779D216","biotype":"protein_coding","ncbi_id":"6143","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L19E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":39200283,"end":39204727,"strand":1,"description":"ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:10312]"}, {"versioned_ensembl_gene_id":"ENSG00000215522.11","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"NTRK4,RTK6,CD167,NEP,PTK3A,CAK,EDDR1","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30870550,"end":30889733,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000081692.12","gene_symbol":"JMJD4","gene_name":"jumonji domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25724]","synonyms":"FLJ12517","biotype":"protein_coding","ncbi_id":"65094","summary":null,"start":227730425,"end":227735411,"strand":-1,"description":"jumonji domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25724]"}, {"versioned_ensembl_gene_id":"ENSG00000230005.2","gene_symbol":"SNAP47-AS1","gene_name":"SNAP47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41501]","synonyms":"SNAP47-IT1","biotype":"antisense_RNA","ncbi_id":"100885800","summary":null,"start":227743831,"end":227747191,"strand":-1,"description":"SNAP47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41501]"}, {"versioned_ensembl_gene_id":"ENSG00000119414.11","gene_symbol":"PPP6C","gene_name":"protein phosphatase 6 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9323]","synonyms":"PP6","biotype":"protein_coding","ncbi_id":"5537","summary":"This gene encodes the catalytic subunit of protein phosphatase, a component of a signaling pathway regulating cell cycle progression. Splice variants encoding different protein isoforms exist. The pseudogene of this gene is located on chromosome X. [provided by RefSeq, Jul 2008]","start":125146573,"end":125189939,"strand":-1,"description":"protein phosphatase 6 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9323]"}, {"versioned_ensembl_gene_id":"ENSG00000126247.10","gene_symbol":"CAPNS1","gene_name":"calpain small subunit 1 [Source:HGNC Symbol;Acc:HGNC:1481]","synonyms":"CAPN4,CANPS,CANP,30K,CDPS","biotype":"protein_coding","ncbi_id":"826","summary":"This gene is a member of the calpain small subunit family. Calpains are calcium-dependent cysteine proteinases that are widely distributed in mammalian cells. Calpains operate as heterodimers, comprising a specific large catalytic subunit (calpain 1 subunit in Calpain I, and calpain 2 subunit in Calpain II), and a common small regulatory subunit encoded by this gene. This encoded protein is essential for the stability and function of both calpain heterodimers, whose proteolytic activities influence various cellular functions including apoptosis, proliferation, migration, adhesion, and autophagy. Calpains have been implicated in neurodegenerative processes, such as myotonic dystrophy. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":36139575,"end":36150353,"strand":1,"description":"calpain small subunit 1 [Source:HGNC Symbol;Acc:HGNC:1481]"}, {"versioned_ensembl_gene_id":"ENSG00000234560.4","gene_symbol":"OR10G8","gene_name":"olfactory receptor family 10 subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:14845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219869","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124026798,"end":124030634,"strand":1,"description":"olfactory receptor family 10 subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:14845]"}, {"versioned_ensembl_gene_id":"ENSG00000236981.1","gene_symbol":"OR10G9","gene_name":"olfactory receptor family 10 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:15129]","synonyms":"OR10G10P","biotype":"protein_coding","ncbi_id":"219870","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124023013,"end":124023948,"strand":1,"description":"olfactory receptor family 10 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:15129]"}, {"versioned_ensembl_gene_id":"ENSG00000224223.1","gene_symbol":"VSTM2A-OT1","gene_name":"VSTM2A overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50770]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"285878","summary":null,"start":54556970,"end":54571726,"strand":1,"description":"VSTM2A overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50770]"}, {"versioned_ensembl_gene_id":"ENSG00000259924.1","gene_symbol":"AC011939.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65771176,"end":65772139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226174.6","gene_symbol":"TEX22","gene_name":"testis expressed 22 [Source:HGNC Symbol;Acc:HGNC:40026]","synonyms":null,"biotype":"protein_coding","ncbi_id":"647310","summary":null,"start":105398579,"end":105450106,"strand":1,"description":"testis expressed 22 [Source:HGNC Symbol;Acc:HGNC:40026]"}, {"versioned_ensembl_gene_id":"ENSG00000263098.1","gene_symbol":"AC068014.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82795486,"end":82796095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235939.1","gene_symbol":"AL138760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49419277,"end":49472903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265625.1","gene_symbol":"AC104564.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29644796,"end":29645847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074621.13","gene_symbol":"SLC24A1","gene_name":"solute carrier family 24 member 1 [Source:HGNC Symbol;Acc:HGNC:10975]","synonyms":"CSNB1D,RODX,NCKX1,NCKX,KIAA0702,HsT17412","biotype":"protein_coding","ncbi_id":"9187","summary":"This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":65611366,"end":65660995,"strand":1,"description":"solute carrier family 24 member 1 [Source:HGNC Symbol;Acc:HGNC:10975]"}, {"versioned_ensembl_gene_id":"ENSG00000107186.16","gene_symbol":"MPDZ","gene_name":"multiple PDZ domain crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:7208]","synonyms":"MUPP1","biotype":"protein_coding","ncbi_id":"8777","summary":"The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":13105704,"end":13279590,"strand":-1,"description":"multiple PDZ domain crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:7208]"}, {"versioned_ensembl_gene_id":"ENSG00000164332.7","gene_symbol":"UBLCP1","gene_name":"ubiquitin like domain containing CTD phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28110]","synonyms":"MGC10067,CPUB1","biotype":"protein_coding","ncbi_id":"134510","summary":null,"start":159263081,"end":159286040,"strand":1,"description":"ubiquitin like domain containing CTD phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28110]"}, {"versioned_ensembl_gene_id":"ENSG00000136631.12","gene_symbol":"VPS45","gene_name":"vacuolar protein sorting 45 homolog [Source:HGNC Symbol;Acc:HGNC:14579]","synonyms":"VPS45B,VPS45A,H1,h-vps45","biotype":"protein_coding","ncbi_id":"11311","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec1 domain family, and shows a high degree of sequence similarity to mouse, rat and yeast Vps45. The exact function of this gene is not known, but its high expression in peripheral blood mononuclear cells suggests a role in trafficking proteins, including inflammatory mediators. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2013]","start":150067293,"end":150145327,"strand":1,"description":"vacuolar protein sorting 45 homolog [Source:HGNC Symbol;Acc:HGNC:14579]"}, {"versioned_ensembl_gene_id":"ENSG00000228877.2","gene_symbol":"AL669970.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134527182,"end":134545244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223795.2","gene_symbol":"AL669970.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134505472,"end":134521442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235191.1","gene_symbol":"NUCB1-AS1","gene_name":"NUCB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40419]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874085","summary":null,"start":48910930,"end":48918891,"strand":-1,"description":"NUCB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40419]"}, {"versioned_ensembl_gene_id":"ENSG00000263321.1","gene_symbol":"AC024361.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82729164,"end":82734143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176840.11","gene_symbol":"MIR7-3HG","gene_name":"MIR7-3 host gene [Source:HGNC Symbol;Acc:HGNC:30049]","synonyms":"NCRNA00306,LINC00306,Huh7,C19orf30,uc002mbe.2,PGSF1b,PGSF1a,PGSF1","biotype":"lincRNA","ncbi_id":"284424","summary":null,"start":4769140,"end":4772533,"strand":1,"description":"MIR7-3 host gene [Source:HGNC Symbol;Acc:HGNC:30049]"}, {"versioned_ensembl_gene_id":"ENSG00000249610.1","gene_symbol":"AC010255.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122154496,"end":122156015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237717.1","gene_symbol":"BX276092.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71744828,"end":71745077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237182.1","gene_symbol":"BX276092.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71736454,"end":71736703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166257.8","gene_symbol":"SCN3B","gene_name":"sodium voltage-gated channel beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:20665]","synonyms":"HSA243396","biotype":"protein_coding","ncbi_id":"55800","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel beta subunit gene family, and influences the inactivation kinetics of the sodium channel. Two alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":123629187,"end":123655244,"strand":-1,"description":"sodium voltage-gated channel beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:20665]"}, {"versioned_ensembl_gene_id":"ENSG00000257838.5","gene_symbol":"AC106788.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22545698,"end":22576865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081148.11","gene_symbol":"IMPG2","gene_name":"interphotoreceptor matrix proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:18362]","synonyms":"RP56,IPM200","biotype":"protein_coding","ncbi_id":"50939","summary":"The protein encoded by this gene binds chondroitin sulfate and hyaluronan and is a proteoglycan. The encoded protein plays a role in the organization of the interphotoreceptor matrix and may promote the growth and maintenance of the light-sensitive photoreceptor outer segment. Defects in this gene are a cause of retinitis pigmentosa type 56 and maculopathy, IMPG2-related.[provided by RefSeq, Mar 2011]","start":101222546,"end":101320560,"strand":-1,"description":"interphotoreceptor matrix proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:18362]"}, {"versioned_ensembl_gene_id":"ENSG00000226705.1","gene_symbol":"SDCBPP1","gene_name":"syndecan binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128930","summary":null,"start":6293100,"end":6294684,"strand":-1,"description":"syndecan binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44684]"}, {"versioned_ensembl_gene_id":"ENSG00000109255.11","gene_symbol":"NMU","gene_name":"neuromedin U [Source:HGNC Symbol;Acc:HGNC:7859]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10874","summary":"This gene encodes a member of the neuromedin family of neuropeptides. The encoded protein is a precursor that is proteolytically processed to generate a biologically active neuropeptide that plays a role in pain, stress, immune-mediated inflammatory diseases and feeding regulation. Increased expression of this gene was observed in renal, pancreatic and lung cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. Some of these isoforms may undergo similar processing to generate the mature peptide. [provided by RefSeq, Jul 2015]","start":55595229,"end":55636698,"strand":-1,"description":"neuromedin U [Source:HGNC Symbol;Acc:HGNC:7859]"}, {"versioned_ensembl_gene_id":"ENSG00000120656.11","gene_symbol":"TAF12","gene_name":"TATA-box binding protein associated factor 12 [Source:HGNC Symbol;Acc:HGNC:11545]","synonyms":"TAFII20,TAF2J","biotype":"protein_coding","ncbi_id":"6883","summary":"Control of transcription by RNA polymerase II involves the basal transcription machinery which is a collection of proteins. These proteins with RNA polymerase II, assemble into complexes which are modulated by transactivator proteins that bind to cis-regulatory elements located adjacent to the transcription start site. Some modulators interact directly with the basal complex, whereas others may act as bridging proteins linking transactivators to the basal transcription factors. Some of these associated factors are weakly attached while others are tightly associated with TBP in the TFIID complex. Among the latter are the TAF proteins. Different TAFs are predicted to mediate the function of distinct transcriptional activators for a variety of gene promoters and RNA polymerases. TAF12 interacts directly with TBP as well as with TAF2I. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2008]","start":28589323,"end":28643085,"strand":-1,"description":"TATA-box binding protein associated factor 12 [Source:HGNC Symbol;Acc:HGNC:11545]"}, {"versioned_ensembl_gene_id":"ENSG00000242573.1","gene_symbol":"ACTR3P3","gene_name":"ACTR3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38679]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128020","summary":null,"start":101163094,"end":101163986,"strand":1,"description":"ACTR3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38679]"}, {"versioned_ensembl_gene_id":"ENSG00000281852.1","gene_symbol":"LINC00891","gene_name":"long intergenic non-protein coding RNA 891 [Source:HGNC Symbol;Acc:HGNC:48577]","synonyms":"FLJ46446","biotype":"lincRNA","ncbi_id":"441501","summary":null,"start":71697196,"end":71706455,"strand":1,"description":"long intergenic non-protein coding RNA 891 [Source:HGNC Symbol;Acc:HGNC:48577]"}, {"versioned_ensembl_gene_id":"ENSG00000278443.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29852167,"end":29852298,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000141580.15","gene_symbol":"WDR45B","gene_name":"WD repeat domain 45B [Source:HGNC Symbol;Acc:HGNC:25072]","synonyms":"WIPI3,WDR45L","biotype":"protein_coding","ncbi_id":"56270","summary":"This gene encodes a member of the WIPI or SVP1 family of WD40 repeat-containing proteins. The protein contains seven WD40 repeats that are thought to fold into a beta-propeller structure that mediates protein-protein interactions, and a conserved motif for interaction with phospholipids. The human genome contains several pseudogenes of this gene. [provided by RefSeq, Jul 2008]","start":82614562,"end":82648553,"strand":-1,"description":"WD repeat domain 45B [Source:HGNC Symbol;Acc:HGNC:25072]"}, {"versioned_ensembl_gene_id":"ENSG00000253207.3","gene_symbol":"AC103993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113600310,"end":113616958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253164.5","gene_symbol":"AC023403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20350210,"end":20372769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249635.1","gene_symbol":"AC109361.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106003317,"end":106022478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232759.1","gene_symbol":"AC002480.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22563337,"end":22573996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228926.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31601835,"end":31602108,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000133195.11","gene_symbol":"SLC39A11","gene_name":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]","synonyms":"C17orf26","biotype":"protein_coding","ncbi_id":"201266","summary":null,"start":72645949,"end":73092712,"strand":-1,"description":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]"}, {"versioned_ensembl_gene_id":"ENSG00000204967.10","gene_symbol":"PCDHA4","gene_name":"protocadherin alpha 4 [Source:HGNC Symbol;Acc:HGNC:8670]","synonyms":"PCDH-ALPHA4,CRNR1,CNRN1,CNR1","biotype":"protein_coding","ncbi_id":"56144","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140806929,"end":141012344,"strand":1,"description":"protocadherin alpha 4 [Source:HGNC Symbol;Acc:HGNC:8670]"}, {"versioned_ensembl_gene_id":"ENSG00000141040.14","gene_symbol":"ZNF287","gene_name":"zinc finger protein 287 [Source:HGNC Symbol;Acc:HGNC:13502]","synonyms":"ZSCAN45,ZKSCAN13","biotype":"protein_coding","ncbi_id":"57336","summary":"This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":16551387,"end":16569206,"strand":-1,"description":"zinc finger protein 287 [Source:HGNC Symbol;Acc:HGNC:13502]"}, {"versioned_ensembl_gene_id":"ENSG00000271044.1","gene_symbol":"AC087468.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84940504,"end":84941133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153822.13","gene_symbol":"KCNJ16","gene_name":"potassium voltage-gated channel subfamily J member 16 [Source:HGNC Symbol;Acc:HGNC:6262]","synonyms":"Kir5.1,BIR9","biotype":"protein_coding","ncbi_id":"3773","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which tends to allow potassium to flow into rather than out of a cell, can form heterodimers with two other inward-rectifier type potassium channels. It may function in fluid and pH balance regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2014]","start":70053429,"end":70135608,"strand":1,"description":"potassium voltage-gated channel subfamily J member 16 [Source:HGNC Symbol;Acc:HGNC:6262]"}, {"versioned_ensembl_gene_id":"ENSG00000204970.9","gene_symbol":"PCDHA1","gene_name":"protocadherin alpha 1 [Source:HGNC Symbol;Acc:HGNC:8663]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56147","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140786136,"end":141012347,"strand":1,"description":"protocadherin alpha 1 [Source:HGNC Symbol;Acc:HGNC:8663]"}, {"versioned_ensembl_gene_id":"ENSG00000237265.6","gene_symbol":"BX276092.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71662998,"end":71666767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237560.5","gene_symbol":"LINC01497","gene_name":"long intergenic non-protein coding RNA 1497 [Source:HGNC Symbol;Acc:HGNC:51163]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723487","summary":null,"start":69961707,"end":69983538,"strand":1,"description":"long intergenic non-protein coding RNA 1497 [Source:HGNC Symbol;Acc:HGNC:51163]"}, {"versioned_ensembl_gene_id":"ENSG00000259760.1","gene_symbol":"AC015660.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99396613,"end":99401315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261523.1","gene_symbol":"AC009167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14695567,"end":14707055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227711.3","gene_symbol":"AL451054.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":227509028,"end":227510618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152822.13","gene_symbol":"GRM1","gene_name":"glutamate metabotropic receptor 1 [Source:HGNC Symbol;Acc:HGNC:4593]","synonyms":"PPP1R85,MGLUR1,mGlu1,GPRC1A","biotype":"protein_coding","ncbi_id":"2911","summary":"This gene encodes a metabotropic glutamate receptor that functions by activating phospholipase C. L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The canonical alpha isoform of the encoded protein is a disulfide-linked homodimer whose activity is mediated by a G-protein-coupled phosphatidylinositol-calcium second messenger system. This gene may be associated with many disease states, including schizophrenia, bipolar disorder, depression, and breast cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":146027646,"end":146437598,"strand":1,"description":"glutamate metabotropic receptor 1 [Source:HGNC Symbol;Acc:HGNC:4593]"}, {"versioned_ensembl_gene_id":"ENSG00000216811.2","gene_symbol":"AL035698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146364931,"end":146365494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116205.12","gene_symbol":"TCEANC2","gene_name":"transcription elongation factor A N-terminal and central domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26494]","synonyms":"FLJ32112,C1orf83","biotype":"protein_coding","ncbi_id":"127428","summary":null,"start":54053587,"end":54112519,"strand":1,"description":"transcription elongation factor A N-terminal and central domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26494]"}, {"versioned_ensembl_gene_id":"ENSG00000226798.1","gene_symbol":"AL138749.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80869758,"end":80871295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256269.7","gene_symbol":"HMBS","gene_name":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]","synonyms":"UPS,PORC,PBGD","biotype":"protein_coding","ncbi_id":"3145","summary":"This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":119084866,"end":119093549,"strand":1,"description":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]"}, {"versioned_ensembl_gene_id":"ENSG00000254856.1","gene_symbol":"NDUFA3P2","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479051","summary":null,"start":68488609,"end":68488840,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45051]"}, {"versioned_ensembl_gene_id":"ENSG00000171552.12","gene_symbol":"BCL2L1","gene_name":"BCL2 like 1 [Source:HGNC Symbol;Acc:HGNC:992]","synonyms":"PPP1R52,BCLX,BCL2L,bcl-xS,bcl-xL,Bcl-X","biotype":"protein_coding","ncbi_id":"598","summary":"The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The proteins encoded by this gene are located at the outer mitochondrial membrane, and have been shown to regulate outer mitochondrial membrane channel (VDAC) opening. VDAC regulates mitochondrial membrane potential, and thus controls the production of reactive oxygen species and release of cytochrome C by mitochondria, both of which are the potent inducers of cell apoptosis. Alternative splicing results in multiple transcript variants encoding two different isoforms. The longer isoform acts as an apoptotic inhibitor and the shorter isoform acts as an apoptotic activator. [provided by RefSeq, Dec 2015]","start":31664452,"end":31723989,"strand":-1,"description":"BCL2 like 1 [Source:HGNC Symbol;Acc:HGNC:992]"}, {"versioned_ensembl_gene_id":"ENSG00000185304.14","gene_symbol":"RGPD2","gene_name":"RANBP2-like and GRIP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32415]","synonyms":"RGP2,RANBP2L2","biotype":"protein_coding","ncbi_id":"729857","summary":null,"start":87755955,"end":87825952,"strand":-1,"description":"RANBP2-like and GRIP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32415]"}, {"versioned_ensembl_gene_id":"ENSG00000184814.5","gene_symbol":"PRR23B","gene_name":"proline rich 23B [Source:HGNC Symbol;Acc:HGNC:33764]","synonyms":"FLJ46116","biotype":"protein_coding","ncbi_id":"389151","summary":null,"start":139019031,"end":139020926,"strand":-1,"description":"proline rich 23B [Source:HGNC Symbol;Acc:HGNC:33764]"}, {"versioned_ensembl_gene_id":"ENSG00000204611.6","gene_symbol":"ZNF616","gene_name":"zinc finger protein 616 [Source:HGNC Symbol;Acc:HGNC:28062]","synonyms":"MGC45556","biotype":"protein_coding","ncbi_id":"90317","summary":null,"start":52113091,"end":52139922,"strand":-1,"description":"zinc finger protein 616 [Source:HGNC Symbol;Acc:HGNC:28062]"}, {"versioned_ensembl_gene_id":"ENSG00000243680.1","gene_symbol":"RPL37P23","gene_name":"ribosomal protein L37 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37003]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648217","summary":null,"start":52143043,"end":52143336,"strand":1,"description":"ribosomal protein L37 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37003]"}, {"versioned_ensembl_gene_id":"ENSG00000279643.3","gene_symbol":"TAMM41","gene_name":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]","synonyms":"MGC16471,DKFZp434E0519,C3orf31","biotype":"protein_coding","ncbi_id":"132001","summary":null,"start":11817080,"end":11846919,"strand":-1,"description":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]"}, {"versioned_ensembl_gene_id":"ENSG00000187024.14","gene_symbol":"PTRH1","gene_name":"peptidyl-tRNA hydrolase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27039]","synonyms":"PTH1,C9orf115","biotype":"protein_coding","ncbi_id":"138428","summary":null,"start":127690348,"end":127724873,"strand":-1,"description":"peptidyl-tRNA hydrolase 1 homolog [Source:HGNC Symbol;Acc:HGNC:27039]"}, {"versioned_ensembl_gene_id":"ENSG00000276858.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874219,"end":54890443,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000241124.1","gene_symbol":"BX248109.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28987721,"end":28989460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163541.11","gene_symbol":"SUCLG1","gene_name":"succinate-CoA ligase alpha subunit [Source:HGNC Symbol;Acc:HGNC:11449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8802","summary":"This gene encodes the alpha subunit of the heterodimeric enzyme succinate coenzyme A ligase. This enzyme is targeted to the mitochondria and catalyzes the conversion of succinyl CoA and ADP or GDP to succinate and ATP or GTP. Mutations in this gene are the cause of the metabolic disorder fatal infantile lactic acidosis and mitochondrial DNA depletion. [provided by RefSeq, Feb 2010]","start":84423523,"end":84460045,"strand":-1,"description":"succinate-CoA ligase alpha subunit [Source:HGNC Symbol;Acc:HGNC:11449]"}, {"versioned_ensembl_gene_id":"ENSG00000121644.18","gene_symbol":"DESI2","gene_name":"desumoylating isopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24264]","synonyms":"FAM152A,CGI-146,C1orf121,PPPDE1,PNAS-4,FLJ21998","biotype":"protein_coding","ncbi_id":"51029","summary":null,"start":244652935,"end":244709033,"strand":1,"description":"desumoylating isopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24264]"}, {"versioned_ensembl_gene_id":"ENSG00000165916.8","gene_symbol":"PSMC3","gene_name":"proteasome 26S subunit, ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9549]","synonyms":"TBP-1,TBP1","biotype":"protein_coding","ncbi_id":"5702","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases that have chaperone-like activity. This subunit may compete with PSMC2 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. A pseudogene has been identified on chromosome 9. [provided by RefSeq, Jul 2008]","start":47418769,"end":47426473,"strand":-1,"description":"proteasome 26S subunit, ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9549]"}, {"versioned_ensembl_gene_id":"ENSG00000206262.8","gene_symbol":"FOXL2NB","gene_name":"FOXL2 neighbor [Source:HGNC Symbol;Acc:HGNC:34428]","synonyms":"FLJ43329,C3orf72","biotype":"protein_coding","ncbi_id":"401089","summary":null,"start":138947234,"end":138953451,"strand":1,"description":"FOXL2 neighbor [Source:HGNC Symbol;Acc:HGNC:34428]"}, {"versioned_ensembl_gene_id":"ENSG00000259317.1","gene_symbol":"AC044860.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85272527,"end":85272974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216444.1","gene_symbol":"RAET1M","gene_name":"retinoic acid early transcript 1M pseudogene [Source:HGNC Symbol;Acc:HGNC:16799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"353094","summary":null,"start":150032769,"end":150033566,"strand":1,"description":"retinoic acid early transcript 1M pseudogene [Source:HGNC Symbol;Acc:HGNC:16799]"}, {"versioned_ensembl_gene_id":"ENSG00000226263.1","gene_symbol":"ISM1-AS1","gene_name":"ISM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44313]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505536","summary":null,"start":13237801,"end":13239674,"strand":-1,"description":"ISM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44313]"}, {"versioned_ensembl_gene_id":"ENSG00000132185.16","gene_symbol":"FCRLA","gene_name":"Fc receptor like A [Source:HGNC Symbol;Acc:HGNC:18504]","synonyms":"MGC4595,FREB,FCRLX,FCRLM1,FCRLe,FCRLd,FCRLc2,FCRLc1,FCRLb,FCRLa,FCRL","biotype":"protein_coding","ncbi_id":"84824","summary":"This gene encodes a protein similar to receptors for the Fc fragment of gamma immunoglobulin (IgG). These receptors, referred to as FCGRs, mediate the destruction of IgG-coated antigens and of cells induced by antibodies. This encoded protein is selectively expressed in B cells, and may be involved in their development. This protein may also be involved in the development of lymphomas. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":161706972,"end":161714352,"strand":1,"description":"Fc receptor like A [Source:HGNC Symbol;Acc:HGNC:18504]"}, {"versioned_ensembl_gene_id":"ENSG00000225230.1","gene_symbol":"AC008937.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56900041,"end":56910714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213075.7","gene_symbol":"RPL31P11","gene_name":"ribosomal protein L31 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35849]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"641311","summary":null,"start":161683695,"end":161685252,"strand":-1,"description":"ribosomal protein L31 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35849]"}, {"versioned_ensembl_gene_id":"ENSG00000259952.1","gene_symbol":"AC009133.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29806496,"end":29807732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163528.12","gene_symbol":"CHCHD4","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26467]","synonyms":"TIMM40,MIA40,FLJ31709","biotype":"protein_coding","ncbi_id":"131474","summary":"CHCHD4, a component of human mitochondria, belongs to a protein family whose members share 6 highly conserved cysteine residues constituting a -CXC-CX(9)C-CX(9)C- motif in the C terminus (Hofmann et al., 2005 [PubMed 16185709]).[supplied by OMIM, Mar 2008]","start":14112077,"end":14124870,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26467]"}, {"versioned_ensembl_gene_id":"ENSG00000224247.1","gene_symbol":"AJ009632.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15493932,"end":15496124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181191.11","gene_symbol":"PJA1","gene_name":"praja ring finger ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:16648]","synonyms":"RNF70,FLJ11830","biotype":"protein_coding","ncbi_id":"64219","summary":"This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":69160851,"end":69165793,"strand":-1,"description":"praja ring finger ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:16648]"}, {"versioned_ensembl_gene_id":"ENSG00000188388.10","gene_symbol":"GOLGA6L3","gene_name":"golgin A6 family-like 3 [Source:HGNC Symbol;Acc:HGNC:37441]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100133220","summary":null,"start":85240472,"end":85247170,"strand":1,"description":"golgin A6 family-like 3 [Source:HGNC Symbol;Acc:HGNC:37441]"}, {"versioned_ensembl_gene_id":"ENSG00000271324.1","gene_symbol":"AC112220.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33793644,"end":33794145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228112.1","gene_symbol":"AC112220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33727250,"end":33727604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264365.1","gene_symbol":"AC023983.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24364787,"end":24367984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229212.7","gene_symbol":"AC044860.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85205440,"end":85234795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259270.1","gene_symbol":"AC044860.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85178628,"end":85178806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272900.1","gene_symbol":"AP000435.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58291826,"end":58292765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282904.1","gene_symbol":"AC107398.4","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":47463784,"end":47470477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267241.2","gene_symbol":"CYP4F10P","gene_name":"cytochrome P450 family 4 subfamily F member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39943]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646575","summary":null,"start":15664106,"end":15669826,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39943]"}, {"versioned_ensembl_gene_id":"ENSG00000141447.17","gene_symbol":"OSBPL1A","gene_name":"oxysterol binding protein like 1A [Source:HGNC Symbol;Acc:HGNC:16398]","synonyms":"OSBPL1B,ORP1,ORP-1","biotype":"protein_coding","ncbi_id":"114876","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although some members contain only the sterol-binding domain. Transcript variants derived from alternative promoter usage and/or alternative splicing exist; they encode different isoforms. [provided by RefSeq, Jul 2008]","start":24162044,"end":24397880,"strand":-1,"description":"oxysterol binding protein like 1A [Source:HGNC Symbol;Acc:HGNC:16398]"}, {"versioned_ensembl_gene_id":"ENSG00000216863.9","gene_symbol":"LY86-AS1","gene_name":"LY86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26593]","synonyms":"LY86AS,FLJ33708,LY86-AS","biotype":"antisense_RNA","ncbi_id":"285780","summary":null,"start":6346465,"end":6622771,"strand":-1,"description":"LY86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26593]"}, {"versioned_ensembl_gene_id":"ENSG00000214184.3","gene_symbol":"GCC2-AS1","gene_name":"GCC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28126]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644903","summary":null,"start":108507515,"end":108534196,"strand":-1,"description":"GCC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28126]"}, {"versioned_ensembl_gene_id":"ENSG00000265750.1","gene_symbol":"AC090772.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24159509,"end":24162211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258336.2","gene_symbol":"DUX4L52","gene_name":"double homeobox 4 like 52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480354","summary":null,"start":61600067,"end":61600843,"strand":-1,"description":"double homeobox 4 like 52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51811]"}, {"versioned_ensembl_gene_id":"ENSG00000279017.1","gene_symbol":"AC098476.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45749627,"end":45750651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155034.18","gene_symbol":"FBXL18","gene_name":"F-box and leucine rich repeat protein 18 [Source:HGNC Symbol;Acc:HGNC:21874]","synonyms":"FLJ11467,Fbl18","biotype":"protein_coding","ncbi_id":"80028","summary":"The protein encoded by this gene is a member of a family of proteins that contain an approximately 40-amino acid F-box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation. The encoded protein has been shown to control the cellular level of FBXL7, a protein that induces mitotic arrest, by targeting it for polyubiquitylation and proteasomal degradation. Members of the F-box protein family, such as FBXL18, are characterized by an approximately 40-amino acid F-box motif. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains. [provided by RefSeq, Mar 2016]","start":5431335,"end":5513798,"strand":-1,"description":"F-box and leucine rich repeat protein 18 [Source:HGNC Symbol;Acc:HGNC:21874]"}, {"versioned_ensembl_gene_id":"ENSG00000166984.11","gene_symbol":"TCP10L2","gene_name":"t-complex 10 like 2 [Source:HGNC Symbol;Acc:HGNC:21254]","synonyms":"bA517H2.3","biotype":"protein_coding","ncbi_id":"401285","summary":null,"start":167146414,"end":167196913,"strand":1,"description":"t-complex 10 like 2 [Source:HGNC Symbol;Acc:HGNC:21254]"}, {"versioned_ensembl_gene_id":"ENSG00000022840.15","gene_symbol":"RNF10","gene_name":"ring finger protein 10 [Source:HGNC Symbol;Acc:HGNC:10055]","synonyms":"RIE2,KIAA0262","biotype":"protein_coding","ncbi_id":"9921","summary":"The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008]","start":120533480,"end":120577594,"strand":1,"description":"ring finger protein 10 [Source:HGNC Symbol;Acc:HGNC:10055]"}, {"versioned_ensembl_gene_id":"ENSG00000243517.1","gene_symbol":"AC024940.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31251992,"end":31252597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120436.3","gene_symbol":"GPR31","gene_name":"G protein-coupled receptor 31 [Source:HGNC Symbol;Acc:HGNC:4486]","synonyms":"HETER1,12-HETER","biotype":"protein_coding","ncbi_id":"2853","summary":null,"start":167156271,"end":167158329,"strand":-1,"description":"G protein-coupled receptor 31 [Source:HGNC Symbol;Acc:HGNC:4486]"}, {"versioned_ensembl_gene_id":"ENSG00000169811.8","gene_symbol":"RBMY1HP","gene_name":"RNA binding motif protein, Y-linked, family 1, member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:9916]","synonyms":"RBMY1H","biotype":"unprocessed_pseudogene","ncbi_id":"5944","summary":null,"start":21493519,"end":21501968,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:9916]"}, {"versioned_ensembl_gene_id":"ENSG00000215604.3","gene_symbol":"ZNF962P","gene_name":"zinc finger protein 962, pseudogene [Source:HGNC Symbol;Acc:HGNC:39250]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729501","summary":null,"start":18467172,"end":18485448,"strand":-1,"description":"zinc finger protein 962, pseudogene [Source:HGNC Symbol;Acc:HGNC:39250]"}, {"versioned_ensembl_gene_id":"ENSG00000182606.14","gene_symbol":"TRAK1","gene_name":"trafficking kinesin protein 1 [Source:HGNC Symbol;Acc:HGNC:29947]","synonyms":"OIP106,MILT1,KIAA1042","biotype":"protein_coding","ncbi_id":"22906","summary":null,"start":42013802,"end":42225889,"strand":1,"description":"trafficking kinesin protein 1 [Source:HGNC Symbol;Acc:HGNC:29947]"}, {"versioned_ensembl_gene_id":"ENSG00000223650.1","gene_symbol":"UHRF2P1","gene_name":"ubiquitin like with PHD and ring finger domains 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"260337","summary":null,"start":74105572,"end":74107958,"strand":1,"description":"ubiquitin like with PHD and ring finger domains 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39565]"}, {"versioned_ensembl_gene_id":"ENSG00000163217.1","gene_symbol":"BMP10","gene_name":"bone morphogenetic protein 10 [Source:HGNC Symbol;Acc:HGNC:20869]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27302","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which binds to the activin receptor-like kinase 1 (ALK1) and plays important roles in cardiovascular development including cardiomyocyte proliferation and regulation of heart size, closure of the ductus arteriosus, angiogenesis and ventricular trabeculation. [provided by RefSeq, Aug 2016]","start":68865481,"end":68871517,"strand":-1,"description":"bone morphogenetic protein 10 [Source:HGNC Symbol;Acc:HGNC:20869]"}, {"versioned_ensembl_gene_id":"ENSG00000232928.2","gene_symbol":"DDX3P1","gene_name":"DEAD-box helicase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42171]","synonyms":"DDX3YP1","biotype":"processed_pseudogene","ncbi_id":"100133180","summary":null,"start":74121012,"end":74131923,"strand":1,"description":"DEAD-box helicase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42171]"}, {"versioned_ensembl_gene_id":"ENSG00000198783.5","gene_symbol":"ZNF830","gene_name":"zinc finger protein 830 [Source:HGNC Symbol;Acc:HGNC:28291]","synonyms":"OMCG1,MGC20398,CCDC16","biotype":"protein_coding","ncbi_id":"91603","summary":null,"start":34961530,"end":34963775,"strand":1,"description":"zinc finger protein 830 [Source:HGNC Symbol;Acc:HGNC:28291]"}, {"versioned_ensembl_gene_id":"ENSG00000256513.1","gene_symbol":"AC022081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28821975,"end":28825831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214896.4","gene_symbol":"RPSAP55","gene_name":"ribosomal protein SA pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388122","summary":null,"start":52885595,"end":52886470,"strand":1,"description":"ribosomal protein SA pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36921]"}, {"versioned_ensembl_gene_id":"ENSG00000083544.13","gene_symbol":"TDRD3","gene_name":"tudor domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20612]","synonyms":"FLJ21007","biotype":"protein_coding","ncbi_id":"81550","summary":null,"start":60396457,"end":60573878,"strand":1,"description":"tudor domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20612]"}, {"versioned_ensembl_gene_id":"ENSG00000011143.16","gene_symbol":"MKS1","gene_name":"Meckel syndrome, type 1 [Source:HGNC Symbol;Acc:HGNC:7121]","synonyms":"POC12,MKS,FLJ20345,BBS13","biotype":"protein_coding","ncbi_id":"54903","summary":"The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":58205437,"end":58219605,"strand":-1,"description":"Meckel syndrome, type 1 [Source:HGNC Symbol;Acc:HGNC:7121]"}, {"versioned_ensembl_gene_id":"ENSG00000229536.2","gene_symbol":"AC079776.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129825126,"end":129877553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265933.5","gene_symbol":"LINC00668","gene_name":"long intergenic non-protein coding RNA 668 [Source:HGNC Symbol;Acc:HGNC:44328]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400643","summary":null,"start":6919496,"end":6929966,"strand":-1,"description":"long intergenic non-protein coding RNA 668 [Source:HGNC Symbol;Acc:HGNC:44328]"}, {"versioned_ensembl_gene_id":"ENSG00000248152.1","gene_symbol":"AC093879.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112979590,"end":113071962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160223.16","gene_symbol":"ICOSLG","gene_name":"inducible T-cell costimulator ligand [Source:HGNC Symbol;Acc:HGNC:17087]","synonyms":"ICOSL,ICOS-L,GL50,CD275,B7RP1,B7RP-1,B7H2,B7-H2,KIAA0653","biotype":"protein_coding","ncbi_id":"23308","summary":null,"start":44222991,"end":44240966,"strand":-1,"description":"inducible T-cell costimulator ligand [Source:HGNC Symbol;Acc:HGNC:17087]"}, {"versioned_ensembl_gene_id":"ENSG00000196218.12","gene_symbol":"RYR1","gene_name":"ryanodine receptor 1 [Source:HGNC Symbol;Acc:HGNC:10483]","synonyms":"RYR,PPP1R137,MHS1,MHS,CCO","biotype":"protein_coding","ncbi_id":"6261","summary":"This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":38433699,"end":38587564,"strand":1,"description":"ryanodine receptor 1 [Source:HGNC Symbol;Acc:HGNC:10483]"}, {"versioned_ensembl_gene_id":"ENSG00000273863.1","gene_symbol":"AC010678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7905536,"end":7907303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000046889.18","gene_symbol":"PREX2","gene_name":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:22950]","synonyms":"PPP1R129,P-REX2,FLJ12987,DEPDC2,DEP.2","biotype":"protein_coding","ncbi_id":"80243","summary":"The protein encoded by this gene belongs to the phosphatidylinositol 3,4,5-trisphosphate (PIP3)-dependent Rac exchanger (PREX) family, which are Dbl-type guanine-nucleotide exchange factors for Rac family small G proteins. Structural domains of this protein include the catalytic diffuse B-cell lymphoma homology and pleckstrin homology (DHPH) domain, two disheveled, EGL-10, and pleckstrin homology (DEP) domains, two PDZ domains, and a C-terminal inositol polyphosphate-4 phosphatase (IP4P) domain that is found in one of the isoforms. This protein facilitates the exchange of GDP for GTP on Rac1, allowing the GTP-bound Rac1 to activate downstream effectors. Studies also show that the pleckstrin homology domain of this protein interacts with the phosphatase and tensin homolog (PTEN) gene product to inhibit PTEN phosphatase activity, thus activating the phosphoinositide-3 kinase (PI3K) signaling pathway. Conversely, the PTEN gene product has also been shown to inhibit the GEF activity of this protein. This gene plays a role in insulin-signaling pathways, and either mutations or overexpression of this gene have been observed in some cancers. [provided by RefSeq, Apr 2016]","start":67952118,"end":68237030,"strand":1,"description":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:22950]"}, {"versioned_ensembl_gene_id":"ENSG00000254051.1","gene_symbol":"AC011853.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68176768,"end":68177221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255206.1","gene_symbol":"AC011853.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68082204,"end":68095081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151498.11","gene_symbol":"ACAD8","gene_name":"acyl-CoA dehydrogenase family member 8 [Source:HGNC Symbol;Acc:HGNC:87]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27034","summary":"This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.[provided by RefSeq, Nov 2009]","start":134253495,"end":134265855,"strand":1,"description":"acyl-CoA dehydrogenase family member 8 [Source:HGNC Symbol;Acc:HGNC:87]"}, {"versioned_ensembl_gene_id":"ENSG00000259740.1","gene_symbol":"AC009558.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47525169,"end":47527756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258885.1","gene_symbol":"AL450267.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36856555,"end":36861375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272966.1","gene_symbol":"AC064836.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":202336739,"end":202337200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175449.13","gene_symbol":"RFESD","gene_name":"Rieske Fe-S domain containing [Source:HGNC Symbol;Acc:HGNC:29587]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317671","summary":null,"start":95646754,"end":95684773,"strand":1,"description":"Rieske Fe-S domain containing [Source:HGNC Symbol;Acc:HGNC:29587]"}, {"versioned_ensembl_gene_id":"ENSG00000229968.1","gene_symbol":"AL022578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47776827,"end":47778697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257146.1","gene_symbol":"AC079905.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59719698,"end":59719944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228186.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"Em:AB014077.1,CAT56,Em:AB023052.2","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30546725,"end":30553562,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000258473.1","gene_symbol":"AC007686.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77048172,"end":77086446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058056.8","gene_symbol":"USP13","gene_name":"ubiquitin specific peptidase 13 (isopeptidase T-3) [Source:HGNC Symbol;Acc:HGNC:12611]","synonyms":"IsoT-3","biotype":"protein_coding","ncbi_id":"8975","summary":null,"start":179652755,"end":179789401,"strand":1,"description":"ubiquitin specific peptidase 13 (isopeptidase T-3) [Source:HGNC Symbol;Acc:HGNC:12611]"}, {"versioned_ensembl_gene_id":"ENSG00000205832.7","gene_symbol":"C16orf96","gene_name":"chromosome 16 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:40031]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342346","summary":null,"start":4556490,"end":4600714,"strand":1,"description":"chromosome 16 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:40031]"}, {"versioned_ensembl_gene_id":"ENSG00000275243.1","gene_symbol":"AC244472.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142598016,"end":142598469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100911.15","gene_symbol":"PSME2","gene_name":"proteasome activator subunit 2 [Source:HGNC Symbol;Acc:HGNC:9569]","synonyms":"PA28beta","biotype":"protein_coding","ncbi_id":"5721","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the beta subunit of the 11S regulator, one of the two 11S subunits that is induced by gamma-interferon. Three beta and three alpha subunits combine to form a heterohexameric ring. Six pseudogenes have been identified on chromosomes 4, 5, 8, 10 and 13. [provided by RefSeq, Jul 2008]","start":24143362,"end":24147570,"strand":-1,"description":"proteasome activator subunit 2 [Source:HGNC Symbol;Acc:HGNC:9569]"}, {"versioned_ensembl_gene_id":"ENSG00000229089.7","gene_symbol":"ANKRD20A8P","gene_name":"ankyrin repeat domain 20 family member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23666]","synonyms":"ANKRD20B","biotype":"protein_coding","ncbi_id":"729171","summary":null,"start":94811046,"end":94857282,"strand":-1,"description":"ankyrin repeat domain 20 family member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23666]"}, {"versioned_ensembl_gene_id":"ENSG00000234315.1","gene_symbol":"OSTCP5","gene_name":"oligosaccharyltransferase complex subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874386","summary":null,"start":45069977,"end":45070429,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42867]"}, {"versioned_ensembl_gene_id":"ENSG00000138152.8","gene_symbol":"BTBD16","gene_name":"BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:26340]","synonyms":"FLJ25359,Em:AC061711.1,C10orf87","biotype":"protein_coding","ncbi_id":"118663","summary":"This gene encodes a protein that contains a BTB/POZ domain. This domain mediates protein-protein interactions. A mutation in this gene may be associated with bipolar disorder. [provided by RefSeq, Sep 2016]","start":122271306,"end":122338162,"strand":1,"description":"BTB domain containing 16 [Source:HGNC Symbol;Acc:HGNC:26340]"}, {"versioned_ensembl_gene_id":"ENSG00000230331.1","gene_symbol":"AL160004.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":229425020,"end":229425650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259064.2","gene_symbol":"AC091544.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92627073,"end":92627414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243538.1","gene_symbol":"RPS26P28","gene_name":"ribosomal protein S26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643003","summary":null,"start":16902294,"end":16902641,"strand":-1,"description":"ribosomal protein S26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36149]"}, {"versioned_ensembl_gene_id":"ENSG00000244302.1","gene_symbol":"PEX5L-AS2","gene_name":"PEX5L antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41252]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928790","summary":null,"start":179898229,"end":179921895,"strand":1,"description":"PEX5L antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41252]"}, {"versioned_ensembl_gene_id":"ENSG00000047188.15","gene_symbol":"YTHDC2","gene_name":"YTH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24721]","synonyms":"FLJ2194,FLJ10053,DKFZp564A186","biotype":"protein_coding","ncbi_id":"64848","summary":"This gene encodes a member of the DEAH (Asp-Glu-Ala-His) subfamily of proteins, part of the DEAD (Asp-Glu-Ala-Asp) box family of RNA helicases. The encoded protein binds to N6-methyladenosine, a common modified RNA nucleotide that is enriched in the stop codons and 3' UTRs of eukaryotic messenger RNAs. Binding of proteins to this modified nucleotide may regulate mRNA translation and stability. This gene may be associated with susceptibility to pancreatic cancer in human patients, and knockdown of this gene resulted in reduced proliferation in a human liver cancer cell line. [provided by RefSeq, Sep 2016]","start":113513683,"end":113595285,"strand":1,"description":"YTH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24721]"}, {"versioned_ensembl_gene_id":"ENSG00000249230.1","gene_symbol":"CDH12P2","gene_name":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]","synonyms":"CDH12P,C41-CAD","biotype":"unprocessed_pseudogene","ncbi_id":"1011","summary":null,"start":69985204,"end":69985501,"strand":-1,"description":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]"}, {"versioned_ensembl_gene_id":"ENSG00000281184.1","gene_symbol":"PSMB1","gene_name":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]","synonyms":"HC5,PMSB1","biotype":"processed_transcript","ncbi_id":"5689","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is tightly linked to the TBP (TATA-binding protein) gene in human and in mouse, and is transcribed in the opposite orientation in both species. [provided by RefSeq, Jul 2008]","start":170544440,"end":170544544,"strand":-1,"description":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]"}, {"versioned_ensembl_gene_id":"ENSG00000280722.1","gene_symbol":"AL008628.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":170423462,"end":170428648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225624.1","gene_symbol":"TBL1YP1","gene_name":"transducin beta like 1, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23979]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"286555","summary":null,"start":20727254,"end":20742900,"strand":1,"description":"transducin beta like 1, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23979]"}, {"versioned_ensembl_gene_id":"ENSG00000063515.2","gene_symbol":"GSC2","gene_name":"goosecoid homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4613]","synonyms":"GSCL","biotype":"protein_coding","ncbi_id":"2928","summary":"Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008]","start":19148576,"end":19150283,"strand":-1,"description":"goosecoid homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4613]"}, {"versioned_ensembl_gene_id":"ENSG00000275158.1","gene_symbol":"AC244196.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142580917,"end":142581427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276953.1","gene_symbol":"AC244196.5","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142563740,"end":142564245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224764.1","gene_symbol":"AL353768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94928551,"end":94934946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183643.4","gene_symbol":"C15orf32","gene_name":"chromosome 15 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26549]","synonyms":"FLJ32831","biotype":"lincRNA","ncbi_id":"145858","summary":null,"start":92471654,"end":92501117,"strand":1,"description":"chromosome 15 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26549]"}, {"versioned_ensembl_gene_id":"ENSG00000089351.14","gene_symbol":"GRAMD1A","gene_name":"GRAM domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29305]","synonyms":"FLJ90346,KIAA1533","biotype":"protein_coding","ncbi_id":"57655","summary":null,"start":34994784,"end":35026471,"strand":1,"description":"GRAM domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29305]"}, {"versioned_ensembl_gene_id":"ENSG00000276405.1","gene_symbol":"AC244196.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142535809,"end":142536292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268678.1","gene_symbol":"AC005261.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57350848,"end":57352012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278030.1","gene_symbol":"TRBV7-9","gene_name":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]","synonyms":"TCRBV6S4A1,TRBV79,TCRBV7S9","biotype":"TR_V_gene","ncbi_id":"28589","summary":null,"start":142529290,"end":142529762,"strand":1,"description":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]"}, {"versioned_ensembl_gene_id":"ENSG00000259443.1","gene_symbol":"AC012414.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20773084,"end":20774871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211731.1","gene_symbol":"TRBV5-7","gene_name":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]","synonyms":"TCRBV5S7,TRBV57,TCRBV5S7P","biotype":"TR_V_gene","ncbi_id":"28608","summary":null,"start":142520090,"end":142520556,"strand":1,"description":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]"}, {"versioned_ensembl_gene_id":"ENSG00000243014.1","gene_symbol":"PTMAP8","gene_name":"prothymosin, alpha pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42437]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728873","summary":null,"start":117026698,"end":117027039,"strand":1,"description":"prothymosin, alpha pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42437]"}, {"versioned_ensembl_gene_id":"ENSG00000108700.4","gene_symbol":"CCL8","gene_name":"C-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:10635]","synonyms":"SCYA8,MCP-2,HC14","biotype":"protein_coding","ncbi_id":"6355","summary":"This antimicrobial gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of N-terminal cysteine residues of the mature peptide. This chemokine is a member of the CC subfamily which is characterized by two adjacent cysteine residues. This cytokine displays chemotactic activity for monocytes, lymphocytes, basophils and eosinophils. By recruiting leukocytes to sites of inflammation this cytokine may contribute to tumor-associated leukocyte infiltration and to the antiviral state against HIV infection. [provided by RefSeq, Sep 2014]","start":34319036,"end":34321402,"strand":1,"description":"C-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:10635]"}, {"versioned_ensembl_gene_id":"ENSG00000250415.1","gene_symbol":"AC022113.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16617225,"end":16621276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241354.2","gene_symbol":"AL049874.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60602146,"end":60602533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175946.8","gene_symbol":"KLHL38","gene_name":"kelch like family member 38 [Source:HGNC Symbol;Acc:HGNC:34435]","synonyms":"C8ORFK36","biotype":"protein_coding","ncbi_id":"340359","summary":null,"start":123645527,"end":123652950,"strand":-1,"description":"kelch like family member 38 [Source:HGNC Symbol;Acc:HGNC:34435]"}, {"versioned_ensembl_gene_id":"ENSG00000267064.1","gene_symbol":"UXT-AS1","gene_name":"UXT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49239]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100133957","summary":null,"start":47658833,"end":47660377,"strand":1,"description":"UXT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49239]"}, {"versioned_ensembl_gene_id":"ENSG00000053371.12","gene_symbol":"AKR7A2","gene_name":"aldo-keto reductase family 7 member A2 [Source:HGNC Symbol;Acc:HGNC:389]","synonyms":"AFAR","biotype":"protein_coding","ncbi_id":"8574","summary":"The protein encoded by this gene belongs to the aldo/keto reductase (AKR) superfamily and AKR7 family, which are involved in the detoxification of aldehydes and ketones. The AKR7 family consists of 3 genes that are present in a cluster on the p arm of chromosome 1. This protein, thought to be localized in the golgi, catalyzes the NADPH-dependent reduction of succinic semialdehyde to the endogenous neuromodulator, gamma-hydroxybutyrate. It may also function as a detoxication enzyme in the reduction of aflatoxin B1 and 2-carboxybenzaldehyde. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":19303965,"end":19312146,"strand":-1,"description":"aldo-keto reductase family 7 member A2 [Source:HGNC Symbol;Acc:HGNC:389]"}, {"versioned_ensembl_gene_id":"ENSG00000218073.1","gene_symbol":"AL021407.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16160926,"end":16161411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241596.1","gene_symbol":"AC092468.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":115658533,"end":115661279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251383.1","gene_symbol":"LINC02483","gene_name":"long intergenic non-protein coding RNA 2483 [Source:HGNC Symbol;Acc:HGNC:53457]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441025","summary":null,"start":75354076,"end":75362566,"strand":1,"description":"long intergenic non-protein coding RNA 2483 [Source:HGNC Symbol;Acc:HGNC:53457]"}, {"versioned_ensembl_gene_id":"ENSG00000270790.1","gene_symbol":"AC025588.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57151587,"end":57151860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151276.23","gene_symbol":"MAGI1","gene_name":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]","synonyms":"BAIAP1,AIP3,WWP3,TNRC19,MAGI-1,BAP1","biotype":"protein_coding","ncbi_id":"9223","summary":"The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":65353525,"end":66038834,"strand":-1,"description":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]"}, {"versioned_ensembl_gene_id":"ENSG00000278042.2","gene_symbol":"IGHV3-72","gene_name":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28410","summary":null,"start":106814867,"end":106815409,"strand":-1,"description":"immunoglobulin heavy variable 3-72 [Source:HGNC Symbol;Acc:HGNC:5622]"}, {"versioned_ensembl_gene_id":"ENSG00000270285.1","gene_symbol":"AC124916.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48039267,"end":48039490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272610.1","gene_symbol":"MAGI1-IT1","gene_name":"MAGI1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42436]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"151877","summary":null,"start":65872815,"end":65954558,"strand":-1,"description":"MAGI1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42436]"}, {"versioned_ensembl_gene_id":"ENSG00000134352.19","gene_symbol":"IL6ST","gene_name":"interleukin 6 signal transducer [Source:HGNC Symbol;Acc:HGNC:6021]","synonyms":"GP130,CD130","biotype":"protein_coding","ncbi_id":"3572","summary":"The protein encoded by this gene is a signal transducer shared by many cytokines, including interleukin 6 (IL6), ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), and oncostatin M (OSM). This protein functions as a part of the cytokine receptor complex. The activation of this protein is dependent upon the binding of cytokines to their receptors. vIL6, a protein related to IL6 and encoded by the Kaposi sarcoma-associated herpesvirus, can bypass the interleukin 6 receptor (IL6R) and directly activate this protein. Knockout studies in mice suggest that this gene plays a critical role in regulating myocyte apoptosis. Alternatively spliced transcript variants have been described. A related pseudogene has been identified on chromosome 17. [provided by RefSeq, May 2014]","start":55935095,"end":55994993,"strand":-1,"description":"interleukin 6 signal transducer [Source:HGNC Symbol;Acc:HGNC:6021]"}, {"versioned_ensembl_gene_id":"ENSG00000255397.1","gene_symbol":"AC022182.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60937705,"end":60939871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235616.1","gene_symbol":"ST13P2","gene_name":"ST13, Hsp70 interacting protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344328","summary":null,"start":187825341,"end":187826449,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38716]"}, {"versioned_ensembl_gene_id":"ENSG00000223583.1","gene_symbol":"AL513365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26454653,"end":26455187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243910.7","gene_symbol":"TUBA4B","gene_name":"tubulin alpha 4b [Source:HGNC Symbol;Acc:HGNC:18637]","synonyms":"TUBA4,FLJ13940","biotype":"protein_coding","ncbi_id":"80086","summary":null,"start":219253243,"end":219272188,"strand":1,"description":"tubulin alpha 4b [Source:HGNC Symbol;Acc:HGNC:18637]"}, {"versioned_ensembl_gene_id":"ENSG00000173627.7","gene_symbol":"APOBEC4","gene_name":"apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 [Source:HGNC Symbol;Acc:HGNC:32152]","synonyms":"FLJ25691,C1orf169,RP1-127C7.4,MGC26594","biotype":"protein_coding","ncbi_id":"403314","summary":"This gene encodes a member of the AID/APOBEC family of polynucleotide (deoxy)cytidine deaminases, which convert cytidine to uridine. Other AID/APOBEC family members are involved in mRNA editing, somatic hypermutation and recombination of immunoglobulin genes, and innate immunity to retroviral infection. [provided by RefSeq, Jul 2008]","start":183646404,"end":183653316,"strand":-1,"description":"apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 [Source:HGNC Symbol;Acc:HGNC:32152]"}, {"versioned_ensembl_gene_id":"ENSG00000253647.1","gene_symbol":"CTD-2270F17.1","gene_name":"uncharacterized LOC101928033 [Source:NCBI gene;Acc:101928033]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928033","summary":null,"start":170389493,"end":170422844,"strand":1,"description":"uncharacterized LOC101928033 [Source:NCBI gene;Acc:101928033]"}, {"versioned_ensembl_gene_id":"ENSG00000236194.3","gene_symbol":"AC099811.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42270517,"end":42272683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119778.14","gene_symbol":"ATAD2B","gene_name":"ATPase family, AAA domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29230]","synonyms":"KIAA1240","biotype":"protein_coding","ncbi_id":"54454","summary":"The protein encoded by this gene belongs to the AAA ATPase family. This family member includes an N-terminal bromodomain. It has been found to be localized to the nucleus, partly to replication sites, consistent with a chromatin-related function. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":23748664,"end":23927114,"strand":-1,"description":"ATPase family, AAA domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29230]"}, {"versioned_ensembl_gene_id":"ENSG00000181201.3","gene_symbol":"HIST3H2BA","gene_name":"histone cluster 3 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20515]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"337872","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 1. [provided by RefSeq, Oct 2015]","start":228464103,"end":228464626,"strand":-1,"description":"histone cluster 3 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20515]"}, {"versioned_ensembl_gene_id":"ENSG00000235172.7","gene_symbol":"LINC01366","gene_name":"long intergenic non-protein coding RNA 1366 [Source:HGNC Symbol;Acc:HGNC:27416]","synonyms":null,"biotype":"lincRNA","ncbi_id":"257358","summary":null,"start":170331429,"end":170333879,"strand":1,"description":"long intergenic non-protein coding RNA 1366 [Source:HGNC Symbol;Acc:HGNC:27416]"}, {"versioned_ensembl_gene_id":"ENSG00000234303.2","gene_symbol":"CLYBL-AS1","gene_name":"CLYBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39893]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927465","summary":null,"start":99726247,"end":99727491,"strand":-1,"description":"CLYBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39893]"}, {"versioned_ensembl_gene_id":"ENSG00000260113.3","gene_symbol":"AC093249.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30626976,"end":30627178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203875.10","gene_symbol":"SNHG5","gene_name":"small nucleolar RNA host gene 5 [Source:HGNC Symbol;Acc:HGNC:21026]","synonyms":"bA33E24.2,U50HG,NCRNA00044,MGC16362,LINC00044,C6orf160","biotype":"processed_transcript","ncbi_id":"387066","summary":"This gene represent a snoRNA host gene and produces a long non-coding RNA. This RNA may regulate gene expression by acting as a sponge for microRNAs. This transcript may also stabilize mRNAs by blocking degradation by staufen double-stranded RNA binding protein 1. [provided by RefSeq, Dec 2017]","start":85660950,"end":85678736,"strand":-1,"description":"small nucleolar RNA host gene 5 [Source:HGNC Symbol;Acc:HGNC:21026]"}, {"versioned_ensembl_gene_id":"ENSG00000188133.5","gene_symbol":"TMEM215","gene_name":"transmembrane protein 215 [Source:HGNC Symbol;Acc:HGNC:33816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401498","summary":null,"start":32783499,"end":32787399,"strand":1,"description":"transmembrane protein 215 [Source:HGNC Symbol;Acc:HGNC:33816]"}, {"versioned_ensembl_gene_id":"ENSG00000067601.7","gene_symbol":"PMS2P4","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9129]","synonyms":"PMS6,PMS2L4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5382","summary":null,"start":67295608,"end":67302907,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9129]"}, {"versioned_ensembl_gene_id":"ENSG00000260835.1","gene_symbol":"AC007223.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6573767,"end":6577359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231563.1","gene_symbol":"AL670729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228407381,"end":228409694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155530.2","gene_symbol":"LRGUK","gene_name":"leucine rich repeats and guanylate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:21964]","synonyms":"FLJ32786,CFAP246","biotype":"protein_coding","ncbi_id":"136332","summary":null,"start":134127299,"end":134264591,"strand":1,"description":"leucine rich repeats and guanylate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:21964]"}, {"versioned_ensembl_gene_id":"ENSG00000270990.1","gene_symbol":"AC069304.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150676833,"end":150677918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239836.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32997896,"end":33033347,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000265618.1","gene_symbol":"AC002094.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28361601,"end":28362859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255443.1","gene_symbol":"CD44-AS1","gene_name":"CD44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40133]","synonyms":"RP1-68D18.4","biotype":"antisense_RNA","ncbi_id":"109729172","summary":null,"start":35210343,"end":35214985,"strand":-1,"description":"CD44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40133]"}, {"versioned_ensembl_gene_id":"ENSG00000277708.1","gene_symbol":"AL118522.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44841925,"end":44842539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163285.7","gene_symbol":"GABRG1","gene_name":"gamma-aminobutyric acid type A receptor gamma1 subunit [Source:HGNC Symbol;Acc:HGNC:4086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2565","summary":"The protein encoded by this gene belongs to the ligand-gated ionic channel family. It is an integral membrane protein and plays an important role in inhibiting neurotransmission by binding to the benzodiazepine receptor and opening an integral chloride channel. This gene is clustered with three other family members on chromosome 4. [provided by RefSeq, Jul 2008]","start":46035769,"end":46124081,"strand":-1,"description":"gamma-aminobutyric acid type A receptor gamma1 subunit [Source:HGNC Symbol;Acc:HGNC:4086]"}, {"versioned_ensembl_gene_id":"ENSG00000211734.3","gene_symbol":"TRBV5-1","gene_name":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]","synonyms":"TRBV51,TCRBV5S1A1T,TCRBV5S1","biotype":"TR_V_gene","ncbi_id":"28614","summary":null,"start":142320677,"end":142321544,"strand":1,"description":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]"}, {"versioned_ensembl_gene_id":"ENSG00000271071.1","gene_symbol":"AL513548.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26611903,"end":26613109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122203.14","gene_symbol":"KIAA1191","gene_name":"KIAA1191 [Source:HGNC Symbol;Acc:HGNC:29209]","synonyms":"p60MONOX,p33MONOX,FLJ21022","biotype":"protein_coding","ncbi_id":"57179","summary":null,"start":176346061,"end":176361968,"strand":-1,"description":"KIAA1191 [Source:HGNC Symbol;Acc:HGNC:29209]"}, {"versioned_ensembl_gene_id":"ENSG00000237702.2","gene_symbol":"TRBV3-1","gene_name":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]","synonyms":"TRBV31,TCRBV9S1A1T,TCRBV3S1","biotype":"TR_V_gene","ncbi_id":"28619","summary":null,"start":142308542,"end":142309048,"strand":1,"description":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]"}, {"versioned_ensembl_gene_id":"ENSG00000229575.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30775289,"end":30776018,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000253361.1","gene_symbol":"AC069120.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38543652,"end":38552680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146109.4","gene_symbol":"ABT1","gene_name":"activator of basal transcription 1 [Source:HGNC Symbol;Acc:HGNC:17369]","synonyms":"Esf2","biotype":"protein_coding","ncbi_id":"29777","summary":"Basal transcription of genes by RNA polymerase II requires the interaction of TATA-binding protein (TBP) with the core region of class II promoters. Studies in mouse suggest that the protein encoded by this gene likely activates basal transcription from class II promoters by interaction with TBP and the class II promoter DNA. [provided by RefSeq, Jul 2008]","start":26596952,"end":26600744,"strand":1,"description":"activator of basal transcription 1 [Source:HGNC Symbol;Acc:HGNC:17369]"}, {"versioned_ensembl_gene_id":"ENSG00000125124.11","gene_symbol":"BBS2","gene_name":"Bardet-Biedl syndrome 2 [Source:HGNC Symbol;Acc:HGNC:967]","synonyms":"BBS","biotype":"protein_coding","ncbi_id":"583","summary":"This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]","start":56466836,"end":56520283,"strand":-1,"description":"Bardet-Biedl syndrome 2 [Source:HGNC Symbol;Acc:HGNC:967]"}, {"versioned_ensembl_gene_id":"ENSG00000276054.1","gene_symbol":"AC243654.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37386886,"end":37387926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282781.1","gene_symbol":"AC093627.21","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164086,"end":167293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059377.16","gene_symbol":"TBXAS1","gene_name":"thromboxane A synthase 1 [Source:HGNC Symbol;Acc:HGNC:11609]","synonyms":"TS,THAS,CYP5A1,CYP5,TXS,TXAS","biotype":"protein_coding","ncbi_id":"6916","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostglandin H2 to thromboxane A2, a potent vasoconstrictor and inducer of platelet aggregation. The enzyme plays a role in several pathophysiological processes including hemostasis, cardiovascular disease, and stroke. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":139777051,"end":140020325,"strand":1,"description":"thromboxane A synthase 1 [Source:HGNC Symbol;Acc:HGNC:11609]"}, {"versioned_ensembl_gene_id":"ENSG00000271711.1","gene_symbol":"AC069236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150611262,"end":150611877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282385.1","gene_symbol":"AC240577.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72839039,"end":72839718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213398.7","gene_symbol":"LCAT","gene_name":"lecithin-cholesterol acyltransferase [Source:HGNC Symbol;Acc:HGNC:6522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3931","summary":"This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008]","start":67939750,"end":67944131,"strand":-1,"description":"lecithin-cholesterol acyltransferase [Source:HGNC Symbol;Acc:HGNC:6522]"}, {"versioned_ensembl_gene_id":"ENSG00000196867.7","gene_symbol":"ZFP28","gene_name":"ZFP28 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:17801]","synonyms":"mkr5,KIAA1431","biotype":"protein_coding","ncbi_id":"140612","summary":null,"start":56538948,"end":56556810,"strand":1,"description":"ZFP28 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:17801]"}, {"versioned_ensembl_gene_id":"ENSG00000269696.1","gene_symbol":"AC005498.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56545566,"end":56567411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172239.13","gene_symbol":"PAIP1","gene_name":"poly(A) binding protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10605","summary":"The protein encoded by this gene interacts with poly(A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":43526267,"end":43557758,"strand":-1,"description":"poly(A) binding protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16945]"}, {"versioned_ensembl_gene_id":"ENSG00000238073.1","gene_symbol":"RBMY2HP","gene_name":"RNA binding motif protein, Y-linked, family 2, member H pseudogene [Source:HGNC Symbol;Acc:HGNC:23893]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378953","summary":null,"start":7671743,"end":7676024,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member H pseudogene [Source:HGNC Symbol;Acc:HGNC:23893]"}, {"versioned_ensembl_gene_id":"ENSG00000274962.1","gene_symbol":"TEX28P1","gene_name":"testis expressed 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33356]","synonyms":"pTEX","biotype":"unprocessed_pseudogene","ncbi_id":"728447","summary":null,"start":154196471,"end":154213487,"strand":-1,"description":"testis expressed 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33356]"}, {"versioned_ensembl_gene_id":"ENSG00000283381.1","gene_symbol":"AC024614.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33692229,"end":33692484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279668.2","gene_symbol":"AC024610.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33827728,"end":34079100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233170.4","gene_symbol":"AC138356.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37747338,"end":37748004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227454.2","gene_symbol":"MTND4P30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42217]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873251","summary":null,"start":202617983,"end":202618881,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42217]"}, {"versioned_ensembl_gene_id":"ENSG00000231398.1","gene_symbol":"AL359385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97275012,"end":97278097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213148.3","gene_symbol":"AC073465.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173431349,"end":173431812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230964.1","gene_symbol":"AC233266.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91578478,"end":91578573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270999.1","gene_symbol":"IGKV1OR2-118","gene_name":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]","synonyms":"IGKV1/OR2-118","biotype":"IG_V_pseudogene","ncbi_id":"339562","summary":null,"start":90315366,"end":90315836,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]"}, {"versioned_ensembl_gene_id":"ENSG00000233714.1","gene_symbol":"AC012506.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23347654,"end":23351864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101901.11","gene_symbol":"ALG13","gene_name":"ALG13, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:30881]","synonyms":"TDRD13,MDS031,GLT28D1,FLJ23018,CXorf45,CDG1S,YGL047W","biotype":"protein_coding","ncbi_id":"79868","summary":"The protein encoded by this gene is a subunit of a bipartite UDP-N-acetylglucosamine transferase. It heterodimerizes with asparagine-linked glycosylation 14 homolog to form a functional UDP-GlcNAc glycosyltransferase that catalyzes the second sugar addition of the highly conserved oligosaccharide precursor in endoplasmic reticulum N-linked glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":111665811,"end":111760649,"strand":1,"description":"ALG13, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:30881]"}, {"versioned_ensembl_gene_id":"ENSG00000268199.2","gene_symbol":"AC010335.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18441419,"end":18443597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258942.1","gene_symbol":"AL358332.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51344914,"end":51385603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148444.15","gene_symbol":"COMMD3","gene_name":"COMM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23332]","synonyms":"C10orf8,BUP","biotype":"protein_coding","ncbi_id":"23412","summary":null,"start":22315974,"end":22320308,"strand":1,"description":"COMM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23332]"}, {"versioned_ensembl_gene_id":"ENSG00000281566.2","gene_symbol":"AL157778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98573859,"end":98864984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224893.5","gene_symbol":"AL160162.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152794496,"end":152831913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185518.11","gene_symbol":"SV2B","gene_name":"synaptic vesicle glycoprotein 2B [Source:HGNC Symbol;Acc:HGNC:16874]","synonyms":"KIAA0735,HsT19680","biotype":"protein_coding","ncbi_id":"9899","summary":"This gene encodes a member of the synaptic vesicle proteins 2 (SV2) family and major facilitator superfamily of proteins. This protein and other members of the family are localized to synaptic vesicles and may function in the regulation of vesicle trafficking and exocytosis. Studies in mice suggest that the encoded protein may act as a protein receptor for botulinum neurotoxin E in neurons, and that this protein may be important for the integrity of the glomerular filtration barrier. This gene shows reduced expression in areas of synaptic loss in the hippocampus of human temporal lobe epilepsy patients. [provided by RefSeq, Sep 2016]","start":91099950,"end":91301309,"strand":1,"description":"synaptic vesicle glycoprotein 2B [Source:HGNC Symbol;Acc:HGNC:16874]"}, {"versioned_ensembl_gene_id":"ENSG00000266282.1","gene_symbol":"UBL5P2","gene_name":"ubiquitin like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287215","summary":null,"start":32227890,"end":32228108,"strand":-1,"description":"ubiquitin like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44640]"}, {"versioned_ensembl_gene_id":"ENSG00000282691.1","gene_symbol":"IGHV4-59","gene_name":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28392","summary":null,"start":106651930,"end":106652506,"strand":-1,"description":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]"}, {"versioned_ensembl_gene_id":"ENSG00000282451.1","gene_symbol":"IGHV4-61","gene_name":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28391","summary":null,"start":106663800,"end":106664338,"strand":-1,"description":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]"}, {"versioned_ensembl_gene_id":"ENSG00000262381.1","gene_symbol":"MTATP6P24","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52180]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075232","summary":null,"start":10724620,"end":10725296,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52180]"}, {"versioned_ensembl_gene_id":"ENSG00000102098.17","gene_symbol":"SCML2","gene_name":"sex comb on midleg like 2 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10389","summary":"This gene encodes a member of the Polycomb group proteins. These proteins form the Polycomb repressive complexes which are involved in transcriptional repression. The encoded protein binds histone peptides that are monomethylated at lysine residues and may be involved in regulating homeotic gene expression during development. [provided by RefSeq, Jun 2010]","start":18239314,"end":18354727,"strand":-1,"description":"sex comb on midleg like 2 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10581]"}, {"versioned_ensembl_gene_id":"ENSG00000273972.1","gene_symbol":"AC068722.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45702640,"end":45703183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138640.14","gene_symbol":"FAM13A","gene_name":"family with sequence similarity 13 member A [Source:HGNC Symbol;Acc:HGNC:19367]","synonyms":"ARHGAP48,KIAA0914,FAM13A1","biotype":"protein_coding","ncbi_id":"10144","summary":null,"start":88725955,"end":89111398,"strand":-1,"description":"family with sequence similarity 13 member A [Source:HGNC Symbol;Acc:HGNC:19367]"}, {"versioned_ensembl_gene_id":"ENSG00000233448.2","gene_symbol":"PMS2P9","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9135]","synonyms":"PMSR5,PMS2LP1,PMS2L17","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132832","summary":null,"start":77039944,"end":77043776,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9135]"}, {"versioned_ensembl_gene_id":"ENSG00000232817.1","gene_symbol":"AC073188.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63388808,"end":63393657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267775.1","gene_symbol":"OR7E16P","gene_name":"olfactory receptor family 7 subfamily E member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:8387]","synonyms":"OR7E60P,OR7E17P,OR19-9,OR19-133","biotype":"unprocessed_pseudogene","ncbi_id":"26473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9191286,"end":9192170,"strand":1,"description":"olfactory receptor family 7 subfamily E member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:8387]"}, {"versioned_ensembl_gene_id":"ENSG00000140265.12","gene_symbol":"ZSCAN29","gene_name":"zinc finger and SCAN domain containing 29 [Source:HGNC Symbol;Acc:HGNC:26673]","synonyms":"ZNF690,Zfp690,FLJ35867","biotype":"protein_coding","ncbi_id":"146050","summary":null,"start":43358172,"end":43371025,"strand":-1,"description":"zinc finger and SCAN domain containing 29 [Source:HGNC Symbol;Acc:HGNC:26673]"}, {"versioned_ensembl_gene_id":"ENSG00000280420.1","gene_symbol":"AC005355.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134522613,"end":134523096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273244.1","gene_symbol":"AC005301.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16676016,"end":16694648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149654.9","gene_symbol":"CDH22","gene_name":"cadherin 22 [Source:HGNC Symbol;Acc:HGNC:13251]","synonyms":"dJ998H6.1,C20orf25","biotype":"protein_coding","ncbi_id":"64405","summary":"This gene is a member of the cadherin superfamily. The gene product is composed of five cadherin repeat domains and a cytoplasmic tail similar to the highly conserved cytoplasmic region of classical cadherins. Expressed predominantly in the brain, this putative calcium-dependent cell adhesion protein may play an important role in morphogenesis and tissue formation in neural and non-neural cells during development and maintenance of the brain and neuroendocrine organs. [provided by RefSeq, Jul 2008]","start":46173733,"end":46308498,"strand":-1,"description":"cadherin 22 [Source:HGNC Symbol;Acc:HGNC:13251]"}, {"versioned_ensembl_gene_id":"ENSG00000243648.1","gene_symbol":"AC109454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134422838,"end":134423335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281975.1","gene_symbol":"AC243615.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16848984,"end":16850544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237190.3","gene_symbol":"CDKN2AIPNL","gene_name":"CDKN2A interacting protein N-terminal like [Source:HGNC Symbol;Acc:HGNC:30545]","synonyms":"MGC13017","biotype":"protein_coding","ncbi_id":"91368","summary":null,"start":134402087,"end":134411898,"strand":-1,"description":"CDKN2A interacting protein N-terminal like [Source:HGNC Symbol;Acc:HGNC:30545]"}, {"versioned_ensembl_gene_id":"ENSG00000267337.1","gene_symbol":"LINC01478","gene_name":"long intergenic non-protein coding RNA 1478 [Source:HGNC Symbol;Acc:HGNC:51121]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927921","summary":null,"start":44323436,"end":44531697,"strand":-1,"description":"long intergenic non-protein coding RNA 1478 [Source:HGNC Symbol;Acc:HGNC:51121]"}, {"versioned_ensembl_gene_id":"ENSG00000260325.1","gene_symbol":"HSPB9","gene_name":"heat shock protein family B (small) member 9 [Source:HGNC Symbol;Acc:HGNC:30589]","synonyms":"CT51","biotype":"protein_coding","ncbi_id":"94086","summary":null,"start":42121431,"end":42123352,"strand":1,"description":"heat shock protein family B (small) member 9 [Source:HGNC Symbol;Acc:HGNC:30589]"}, {"versioned_ensembl_gene_id":"ENSG00000197142.10","gene_symbol":"ACSL5","gene_name":"acyl-CoA synthetase long chain family member 5 [Source:HGNC Symbol;Acc:HGNC:16526]","synonyms":"FACL5,ACS5,ACS2","biotype":"protein_coding","ncbi_id":"51703","summary":"The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas. This gene functions in mediating fatty acid-induced glioma cell growth. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":112374018,"end":112428380,"strand":1,"description":"acyl-CoA synthetase long chain family member 5 [Source:HGNC Symbol;Acc:HGNC:16526]"}, {"versioned_ensembl_gene_id":"ENSG00000172594.12","gene_symbol":"SMPDL3A","gene_name":"sphingomyelin phosphodiesterase acid like 3A [Source:HGNC Symbol;Acc:HGNC:17389]","synonyms":"yR36GH4.1,FLJ20177,ASML3a,ASM3A","biotype":"protein_coding","ncbi_id":"10924","summary":null,"start":122789049,"end":122809720,"strand":1,"description":"sphingomyelin phosphodiesterase acid like 3A [Source:HGNC Symbol;Acc:HGNC:17389]"}, {"versioned_ensembl_gene_id":"ENSG00000234979.1","gene_symbol":"Z82185.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36816326,"end":36819736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273807.2","gene_symbol":"AC244489.1","gene_name":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16418201,"end":16436927,"strand":1,"description":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]"}, {"versioned_ensembl_gene_id":"ENSG00000111913.17","gene_symbol":"RIPOR2","gene_name":"RHO family interacting cell polarization regulator 2 [Source:HGNC Symbol;Acc:HGNC:13872]","synonyms":"MYONAP,KIAA0386,FAM65B,DIFF48,C6orf32","biotype":"protein_coding","ncbi_id":"9750","summary":"This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients. [provided by RefSeq, Sep 2016]","start":24804282,"end":25042018,"strand":-1,"description":"RHO family interacting cell polarization regulator 2 [Source:HGNC Symbol;Acc:HGNC:13872]"}, {"versioned_ensembl_gene_id":"ENSG00000279585.1","gene_symbol":"AL109653.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145797375,"end":145798439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211633.3","gene_symbol":"IGKV1D-42","gene_name":"immunoglobulin kappa variable 1D-42 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5757]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28892","summary":null,"start":90190193,"end":90190681,"strand":1,"description":"immunoglobulin kappa variable 1D-42 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5757]"}, {"versioned_ensembl_gene_id":"ENSG00000196943.12","gene_symbol":"NOP9","gene_name":"NOP9 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:19826]","synonyms":"C14orf21","biotype":"protein_coding","ncbi_id":"161424","summary":null,"start":24299862,"end":24309124,"strand":1,"description":"NOP9 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:19826]"}, {"versioned_ensembl_gene_id":"ENSG00000101911.12","gene_symbol":"PRPS2","gene_name":"phosphoribosyl pyrophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:9465]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5634","summary":"This gene encodes a phosphoribosyl pyrophosphate synthetase that plays a central role in the synthesis of purines and pyrimidines. The encoded protein catalyzes the synthesis of 5-phosphoribosyl 1-pyrophosphate from ATP and D-ribose 5-phosphate. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":12791355,"end":12824222,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:9465]"}, {"versioned_ensembl_gene_id":"ENSG00000157593.18","gene_symbol":"SLC35B2","gene_name":"solute carrier family 35 member B2 [Source:HGNC Symbol;Acc:HGNC:16872]","synonyms":"UGTrel4","biotype":"protein_coding","ncbi_id":"347734","summary":"Sulfotransferases (e.g., SULT4A1; MIM 608359) use an activated form of sulfate, 3-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS), as a common sulfate donor for sulfation of glycoproteins, proteoglycans, and glycolipids in the endoplasmic reticulum and Golgi apparatus. SLC35B2 is located in the microsomal membrane and transports PAPS from the cytosol, where it is synthesized, into the Golgi lumen (Kamiyama et al., 2003 [PubMed 12716889]).[supplied by OMIM, Mar 2008]","start":44254096,"end":44257890,"strand":-1,"description":"solute carrier family 35 member B2 [Source:HGNC Symbol;Acc:HGNC:16872]"}, {"versioned_ensembl_gene_id":"ENSG00000159904.11","gene_symbol":"ZNF890P","gene_name":"zinc finger protein 890, pseudogene [Source:HGNC Symbol;Acc:HGNC:38691]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645700","summary":null,"start":5121239,"end":5144546,"strand":-1,"description":"zinc finger protein 890, pseudogene [Source:HGNC Symbol;Acc:HGNC:38691]"}, {"versioned_ensembl_gene_id":"ENSG00000253138.5","gene_symbol":"LINC00967","gene_name":"long intergenic non-protein coding RNA 967 [Source:HGNC Symbol;Acc:HGNC:48725]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505659","summary":null,"start":66192093,"end":66197315,"strand":1,"description":"long intergenic non-protein coding RNA 967 [Source:HGNC Symbol;Acc:HGNC:48725]"}, {"versioned_ensembl_gene_id":"ENSG00000214281.3","gene_symbol":"HMGN2P39","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874483","summary":null,"start":59010332,"end":59010604,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39410]"}, {"versioned_ensembl_gene_id":"ENSG00000274413.1","gene_symbol":"AC011476.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55035708,"end":55062043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243550.2","gene_symbol":"LINC01214","gene_name":"long intergenic non-protein coding RNA 1214 [Source:HGNC Symbol;Acc:HGNC:49650]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928022","summary":null,"start":150265412,"end":150287373,"strand":-1,"description":"long intergenic non-protein coding RNA 1214 [Source:HGNC Symbol;Acc:HGNC:49650]"}, {"versioned_ensembl_gene_id":"ENSG00000240356.6","gene_symbol":"RPL23AP7","gene_name":"ribosomal protein L23a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:17336]","synonyms":"RPL23AL1,bA395L14.9","biotype":"transcribed_processed_pseudogene","ncbi_id":"118433","summary":null,"start":113610502,"end":113627090,"strand":-1,"description":"ribosomal protein L23a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:17336]"}, {"versioned_ensembl_gene_id":"ENSG00000283016.1","gene_symbol":"AL139353.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31320224,"end":31320634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259512.3","gene_symbol":"HNRNPA1P5","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15787]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506712","summary":null,"start":67627852,"end":67629135,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15787]"}, {"versioned_ensembl_gene_id":"ENSG00000225386.1","gene_symbol":"AC099754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26619330,"end":26622690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234751.1","gene_symbol":"AP002381.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72940498,"end":72941112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230709.1","gene_symbol":"AC104024.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16975999,"end":16981353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274782.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769765,"end":54784000,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000240951.1","gene_symbol":"MTCO2P6","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52022]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075266","summary":null,"start":89587886,"end":89588570,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52022]"}, {"versioned_ensembl_gene_id":"ENSG00000277292.2","gene_symbol":"PIP4K2B","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]","synonyms":"PIP5KIIbeta,PIP5KIIB,PIP5K2B","biotype":"protein_coding","ncbi_id":"8396","summary":"The protein encoded by this gene catalyzes the phosphorylation of phosphatidylinositol-5-phosphate on the fourth hydroxyl of the myo-inositol ring to form phosphatidylinositol-5,4-bisphosphate. This gene is a member of the phosphatidylinositol-5-phosphate 4-kinase family. The encoded protein sequence does not show similarity to other kinases, but the protein does exhibit kinase activity. Additionally, the encoded protein interacts with p55 TNF receptor. [provided by RefSeq, Jul 2008]","start":38566476,"end":38600913,"strand":-1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:8998]"}, {"versioned_ensembl_gene_id":"ENSG00000182652.2","gene_symbol":"OR4Q3","gene_name":"olfactory receptor family 4 subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:15426]","synonyms":"OR4Q4,C14orf13","biotype":"protein_coding","ncbi_id":"441669","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19743571,"end":19749469,"strand":1,"description":"olfactory receptor family 4 subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:15426]"}, {"versioned_ensembl_gene_id":"ENSG00000203546.7","gene_symbol":"AL139353.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31334312,"end":31457441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176312.4","gene_symbol":"OR4H12P","gene_name":"olfactory receptor family 4 subfamily H member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19433]","synonyms":"OR4H12,C14orf14","biotype":"unprocessed_pseudogene","ncbi_id":"161271","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19759868,"end":19760774,"strand":1,"description":"olfactory receptor family 4 subfamily H member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19433]"}, {"versioned_ensembl_gene_id":"ENSG00000175756.13","gene_symbol":"AURKAIP1","gene_name":"aurora kinase A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24114]","synonyms":"FLJ20608,AKIP,AIP","biotype":"protein_coding","ncbi_id":"54998","summary":null,"start":1373730,"end":1375495,"strand":-1,"description":"aurora kinase A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24114]"}, {"versioned_ensembl_gene_id":"ENSG00000272839.1","gene_symbol":"AC011899.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157868538,"end":157869154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258438.3","gene_symbol":"AL512310.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19733355,"end":19734302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257831.1","gene_symbol":"AL136418.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31248628,"end":31302739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101098.12","gene_symbol":"RIMS4","gene_name":"regulating synaptic membrane exocytosis 4 [Source:HGNC Symbol;Acc:HGNC:16183]","synonyms":"dJ781B1.3,C20orf190","biotype":"protein_coding","ncbi_id":"140730","summary":null,"start":44751808,"end":44810338,"strand":-1,"description":"regulating synaptic membrane exocytosis 4 [Source:HGNC Symbol;Acc:HGNC:16183]"}, {"versioned_ensembl_gene_id":"ENSG00000278540.4","gene_symbol":"ACACA","gene_name":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]","synonyms":"ACC,ACAC,ACC1","biotype":"protein_coding","ncbi_id":"31","summary":"Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5' sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":37084988,"end":37406818,"strand":-1,"description":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]"}, {"versioned_ensembl_gene_id":"ENSG00000170923.3","gene_symbol":"OR7G2","gene_name":"olfactory receptor family 7 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8466]","synonyms":"OST260","biotype":"protein_coding","ncbi_id":"390882","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9100407,"end":9107475,"strand":-1,"description":"olfactory receptor family 7 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8466]"}, {"versioned_ensembl_gene_id":"ENSG00000145949.9","gene_symbol":"MYLK4","gene_name":"myosin light chain kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:27972]","synonyms":"SgK085","biotype":"protein_coding","ncbi_id":"340156","summary":null,"start":2663629,"end":2750966,"strand":-1,"description":"myosin light chain kinase family member 4 [Source:HGNC Symbol;Acc:HGNC:27972]"}, {"versioned_ensembl_gene_id":"ENSG00000267796.7","gene_symbol":"LIN37","gene_name":"lin-37 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:33234]","synonyms":"ZK418.4,lin-37,F25965","biotype":"protein_coding","ncbi_id":"55957","summary":"This gene encodes a protein expressed in the eye. [provided by RefSeq, Jul 2008]","start":35748361,"end":35754519,"strand":1,"description":"lin-37 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:33234]"}, {"versioned_ensembl_gene_id":"ENSG00000170929.6","gene_symbol":"OR1M1","gene_name":"olfactory receptor family 1 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8220]","synonyms":"OR19-6","biotype":"protein_coding","ncbi_id":"125963","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9087061,"end":9095669,"strand":1,"description":"olfactory receptor family 1 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8220]"}, {"versioned_ensembl_gene_id":"ENSG00000267154.1","gene_symbol":"OR1M4P","gene_name":"olfactory receptor family 1 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31244]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403232","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9083112,"end":9083398,"strand":-1,"description":"olfactory receptor family 1 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31244]"}, {"versioned_ensembl_gene_id":"ENSG00000214708.4","gene_symbol":"AC116407.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32141226,"end":32143135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280033.1","gene_symbol":"AC116407.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32159311,"end":32160371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280020.1","gene_symbol":"AC116407.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32178946,"end":32180074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182585.9","gene_symbol":"EPGN","gene_name":"epithelial mitogen [Source:HGNC Symbol;Acc:HGNC:17470]","synonyms":"PRO9904,epigen,EPG,ALGV3072","biotype":"protein_coding","ncbi_id":"255324","summary":"The protein encoded by this gene is a member of the epidermal growth factor family. Members of this family are ligands for the epidermal growth factor receptor and play a role in cell survival, proliferation and migration. This protein has been reported to have high mitogenic activity but low affinity for its receptor. Expression of this transcript and protein have been reported in cancer specimens of the breast, bladder, and prostate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":74308473,"end":74315307,"strand":1,"description":"epithelial mitogen [Source:HGNC Symbol;Acc:HGNC:17470]"}, {"versioned_ensembl_gene_id":"ENSG00000279233.1","gene_symbol":"AC122688.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125138245,"end":125141711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282084.1","gene_symbol":"UBE2Q2P2","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]","synonyms":"UBE2QP2,UBE2Q2P3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100134869","summary":null,"start":82434179,"end":82499143,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]"}, {"versioned_ensembl_gene_id":"ENSG00000133317.14","gene_symbol":"LGALS12","gene_name":"galectin 12 [Source:HGNC Symbol;Acc:HGNC:15788]","synonyms":"GRIP1","biotype":"protein_coding","ncbi_id":"85329","summary":"This gene encodes a member of the galectin superfamily, a group of beta-galactoside-binding proteins with conserved carbohydrate recognition domains. The related mouse protein is a primary regulator of the early stages of adipose tissue development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]","start":63506084,"end":63516774,"strand":1,"description":"galectin 12 [Source:HGNC Symbol;Acc:HGNC:15788]"}, {"versioned_ensembl_gene_id":"ENSG00000101017.13","gene_symbol":"CD40","gene_name":"CD40 molecule [Source:HGNC Symbol;Acc:HGNC:11919]","synonyms":"TNFRSF5,p50,Bp50","biotype":"protein_coding","ncbi_id":"958","summary":"This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2014]","start":46118272,"end":46129863,"strand":1,"description":"CD40 molecule [Source:HGNC Symbol;Acc:HGNC:11919]"}, {"versioned_ensembl_gene_id":"ENSG00000198198.15","gene_symbol":"SZT2","gene_name":"SZT2, KICSTOR complex subunit [Source:HGNC Symbol;Acc:HGNC:29040]","synonyms":"FLJ10387,C1orf84,SZT2B,SZT2A,RP11-506B15.1,KIAA0467,FLJ34502","biotype":"protein_coding","ncbi_id":"23334","summary":"The protein encoded by this gene is expressed in the brain, predominantly in the parietal and frontal cortex as well as in dorsal root ganglia. It is localized to the peroxisome, and is implicated in resistance to oxidative stress. It likely functions by increasing superoxide dismutase (SOD) activity, but itself has no direct SOD activity. Studies in mice show that this gene confers low seizure threshold, and may also enhance epileptogenesis. [provided by RefSeq, Jun 2011]","start":43389882,"end":43454247,"strand":1,"description":"SZT2, KICSTOR complex subunit [Source:HGNC Symbol;Acc:HGNC:29040]"}, {"versioned_ensembl_gene_id":"ENSG00000257159.1","gene_symbol":"AC084033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57967058,"end":57968399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255857.5","gene_symbol":"PXN-AS1","gene_name":"PXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44123]","synonyms":"EyeLinc4","biotype":"antisense_RNA","ncbi_id":"100506649","summary":null,"start":120201291,"end":120213138,"strand":1,"description":"PXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44123]"}, {"versioned_ensembl_gene_id":"ENSG00000100181.22","gene_symbol":"TPTEP1","gene_name":"transmembrane phosphatase with tensin homology pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43648]","synonyms":"psiTPTE22","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387590","summary":null,"start":16601887,"end":16698742,"strand":1,"description":"transmembrane phosphatase with tensin homology pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43648]"}, {"versioned_ensembl_gene_id":"ENSG00000274320.2","gene_symbol":"GOLGA6L9","gene_name":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]","synonyms":"GOLGA6L20","biotype":"protein_coding","ncbi_id":"440295","summary":null,"start":82509086,"end":82518216,"strand":1,"description":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]"}, {"versioned_ensembl_gene_id":"ENSG00000235804.2","gene_symbol":"AL357078.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65077413,"end":65078131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274904.1","gene_symbol":"AC093512.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30064306,"end":30064825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163746.11","gene_symbol":"PLSCR2","gene_name":"phospholipid scramblase 2 [Source:HGNC Symbol;Acc:HGNC:16494]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57047","summary":"This gene encodes a member of the phospholipid scramblase family. Phospholipid scramblases are membrane proteins that mediate calcium-dependent, non-specific movement of plasma membrane phospholipids and phosphatidylserine exposure. The encoded protein contains a low affinity calcium binding motif and may play a role in blood coagulation and apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":146391421,"end":146495991,"strand":-1,"description":"phospholipid scramblase 2 [Source:HGNC Symbol;Acc:HGNC:16494]"}, {"versioned_ensembl_gene_id":"ENSG00000241358.1","gene_symbol":"AC069528.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":146391363,"end":146416603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240668.1","gene_symbol":"KRT8P36","gene_name":"keratin 8 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39870]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418748","summary":null,"start":138101478,"end":138102917,"strand":-1,"description":"keratin 8 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39870]"}, {"versioned_ensembl_gene_id":"ENSG00000140379.7","gene_symbol":"BCL2A1","gene_name":"BCL2 related protein A1 [Source:HGNC Symbol;Acc:HGNC:991]","synonyms":"GRS,BFL1,BCL2L5,ACC2,ACC1,ACC-2,ACC-1,HBPA1","biotype":"protein_coding","ncbi_id":"597","summary":"This gene encodes a member of the BCL-2 protein family. The proteins of this family form hetero- or homodimers and act as anti- and pro-apoptotic regulators that are involved in a wide variety of cellular activities such as embryonic development, homeostasis and tumorigenesis. The protein encoded by this gene is able to reduce the release of pro-apoptotic cytochrome c from mitochondria and block caspase activation. This gene is a direct transcription target of NF-kappa B in response to inflammatory mediators, and is up-regulated by different extracellular signals, such as granulocyte-macrophage colony-stimulating factor (GM-CSF), CD40, phorbol ester and inflammatory cytokine TNF and IL-1, which suggests a cytoprotective function that is essential for lymphocyte activation as well as cell survival. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":79960889,"end":79971446,"strand":-1,"description":"BCL2 related protein A1 [Source:HGNC Symbol;Acc:HGNC:991]"}, {"versioned_ensembl_gene_id":"ENSG00000283866.1","gene_symbol":"AP000842.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125957900,"end":125958647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236409.2","gene_symbol":"NRADDP","gene_name":"neurotrophin receptor associated death domain, pseudogene [Source:HGNC Symbol;Acc:HGNC:19337]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"100129354","summary":"The neurotrophin receptor alike death domain proteins belong to the death domain superfamily and are involved in mediating apoptosis. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008]","start":47010824,"end":47013465,"strand":1,"description":"neurotrophin receptor associated death domain, pseudogene [Source:HGNC Symbol;Acc:HGNC:19337]"}, {"versioned_ensembl_gene_id":"ENSG00000256504.2","gene_symbol":"AC009509.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27704568,"end":27708365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174236.3","gene_symbol":"REP15","gene_name":"RAB15 effector protein [Source:HGNC Symbol;Acc:HGNC:33748]","synonyms":"RAB15EP","biotype":"protein_coding","ncbi_id":"387849","summary":"The protein encoded by this intronless gene interacts with GTP-bound Rab15 and is involved in recycling of transferrin receptor from the endocytic recycling compartment to the cell surface. [provided by RefSeq, Sep 2016]","start":27696519,"end":27697596,"strand":1,"description":"RAB15 effector protein [Source:HGNC Symbol;Acc:HGNC:33748]"}, {"versioned_ensembl_gene_id":"ENSG00000169057.21","gene_symbol":"MECP2","gene_name":"methyl-CpG binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6990]","synonyms":"RTT,MRX79,MRX16","biotype":"protein_coding","ncbi_id":"4204","summary":"DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of cognitive disability in females. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]","start":154021573,"end":154137103,"strand":-1,"description":"methyl-CpG binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6990]"}, {"versioned_ensembl_gene_id":"ENSG00000205155.7","gene_symbol":"PSENEN","gene_name":"presenilin enhancer gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:30100]","synonyms":"PEN2","biotype":"protein_coding","ncbi_id":"55851","summary":"Presenilins, which are components of the gamma-secretase protein complex, are required for intramembranous processing of some type I transmembrane proteins, such as the Notch proteins and the beta-amyloid precursor protein. Signaling by Notch receptors mediates a wide range of developmental cell fates. Processing of the beta-amyloid precursor protein generates neurotoxic amyloid beta peptides, the major component of senile plaques associated with Alzheimer's disease. This gene encodes a protein that is required for Notch pathway signaling, and for the activity and accumulation of gamma-secretase. Mutations resulting in haploinsufficiency for this gene cause familial acne inversa-2 (ACNINV2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":35745114,"end":35747519,"strand":1,"description":"presenilin enhancer gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:30100]"}, {"versioned_ensembl_gene_id":"ENSG00000275296.1","gene_symbol":"AC241377.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121058948,"end":121059353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281344.1","gene_symbol":"HELLPAR","gene_name":"HELLP associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43984]","synonyms":"LINC-HELLP","biotype":"macro_lncRNA","ncbi_id":"101101692","summary":null,"start":102197585,"end":102402596,"strand":1,"description":"HELLP associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43984]"}, {"versioned_ensembl_gene_id":"ENSG00000274129.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,LENG5,LENG5,SEN34,SEN34,SEN34L","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190535,"end":54195132,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000256463.8","gene_symbol":"SALL3","gene_name":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]","synonyms":"ZNF796","biotype":"protein_coding","ncbi_id":"27164","summary":"This gene encodes a sal-like C2H2-type zinc-finger protein, and belongs to a family of evolutionarily conserved genes found in species as diverse as Drosophila, C. elegans, and vertebrates. Mutations in some of these genes are associated with congenital disorders in human, suggesting their importance in embryonic development. This protein binds to DNA methyltransferase 3 alpha (DNMT3A), and reduces DNMT3A-mediated CpG island methylation. It is suggested that silencing of this gene, resulting in acceleration of DNA methylation, may have a role in oncogenesis. [provided by RefSeq, Oct 2011]","start":78980275,"end":79002677,"strand":1,"description":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]"}, {"versioned_ensembl_gene_id":"ENSG00000277511.1","gene_symbol":"AC116407.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32127595,"end":32128454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103257.8","gene_symbol":"SLC7A5","gene_name":"solute carrier family 7 member 5 [Source:HGNC Symbol;Acc:HGNC:11063]","synonyms":"CD98,MPE16,LAT1,E16,D16S469E","biotype":"protein_coding","ncbi_id":"8140","summary":null,"start":87830023,"end":87869488,"strand":-1,"description":"solute carrier family 7 member 5 [Source:HGNC Symbol;Acc:HGNC:11063]"}, {"versioned_ensembl_gene_id":"ENSG00000267549.5","gene_symbol":"AC006116.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56314703,"end":56341287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266932.1","gene_symbol":"AC006116.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":56342432,"end":56343419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132872.11","gene_symbol":"SYT4","gene_name":"synaptotagmin 4 [Source:HGNC Symbol;Acc:HGNC:11512]","synonyms":"KIAA1342,HsT1192","biotype":"protein_coding","ncbi_id":"6860","summary":null,"start":43267878,"end":43277650,"strand":-1,"description":"synaptotagmin 4 [Source:HGNC Symbol;Acc:HGNC:11512]"}, {"versioned_ensembl_gene_id":"ENSG00000280168.1","gene_symbol":"AC005274.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":12973033,"end":12973834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169933.13","gene_symbol":"FRMPD4","gene_name":"FERM and PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29007]","synonyms":"PDZK10,PDZD10,KIAA0316","biotype":"protein_coding","ncbi_id":"9758","summary":"This gene encodes a multi-domain (WW, PDZ, FERM) containing protein. Through its interaction with other proteins (such as PSD-95), it functions as a positive regulator of dendritic spine morphogenesis and density, and is required for the maintenance of excitatory synaptic transmission. [provided by RefSeq, Jan 2010]","start":12138466,"end":12724523,"strand":1,"description":"FERM and PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29007]"}, {"versioned_ensembl_gene_id":"ENSG00000250961.1","gene_symbol":"AC025470.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57395060,"end":57533424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234658.1","gene_symbol":"AC013429.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138645671,"end":138646448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234770.1","gene_symbol":"GULOP","gene_name":"gulonolactone (L-) oxidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:4695]","synonyms":"scurvy,GULO","biotype":"unitary_pseudogene","ncbi_id":"2989","summary":"This gene is nonfunctional in humans and other primates. In most mammalian species the corresponding gene encodes L-gulono-gamma-lactone oxidase which catalyzes the last step of ascorbic acid biosynthesis. The human gene is a remnant that lacks five of twelve exons found in functional rodent genes. The loss of enzyme activity results in hypoascorbemia or the inability to synthesize vitamin C. [provided by RefSeq, Nov 2010]","start":27560274,"end":27589073,"strand":1,"description":"gulonolactone (L-) oxidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:4695]"}, {"versioned_ensembl_gene_id":"ENSG00000154370.15","gene_symbol":"TRIM11","gene_name":"tripartite motif containing 11 [Source:HGNC Symbol;Acc:HGNC:16281]","synonyms":"RNF92,BIA1","biotype":"protein_coding","ncbi_id":"81559","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nucleus and the cytoplasm. Its function has not been identified. [provided by RefSeq, Jul 2008]","start":228393673,"end":228406840,"strand":-1,"description":"tripartite motif containing 11 [Source:HGNC Symbol;Acc:HGNC:16281]"}, {"versioned_ensembl_gene_id":"ENSG00000218980.2","gene_symbol":"FTH1P15","gene_name":"ferritin heavy chain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3985]","synonyms":"FTHL15","biotype":"processed_pseudogene","ncbi_id":"2507","summary":null,"start":57004520,"end":57004799,"strand":1,"description":"ferritin heavy chain 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3985]"}, {"versioned_ensembl_gene_id":"ENSG00000240122.1","gene_symbol":"FABP5P11","gene_name":"fatty acid binding protein 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19328]","synonyms":"FABP5P1,FABP5L11","biotype":"processed_pseudogene","ncbi_id":"266699","summary":null,"start":16595089,"end":16595485,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19328]"}, {"versioned_ensembl_gene_id":"ENSG00000155957.17","gene_symbol":"TMBIM4","gene_name":"transmembrane BAX inhibitor motif containing 4 [Source:HGNC Symbol;Acc:HGNC:24257]","synonyms":"S1R,LFG4,GAAP,CGI-119,ZPRO","biotype":"protein_coding","ncbi_id":"51643","summary":null,"start":66135846,"end":66170072,"strand":-1,"description":"transmembrane BAX inhibitor motif containing 4 [Source:HGNC Symbol;Acc:HGNC:24257]"}, {"versioned_ensembl_gene_id":"ENSG00000154319.14","gene_symbol":"FAM167A","gene_name":"family with sequence similarity 167 member A [Source:HGNC Symbol;Acc:HGNC:15549]","synonyms":"C8orf13","biotype":"protein_coding","ncbi_id":"83648","summary":null,"start":11421463,"end":11474715,"strand":-1,"description":"family with sequence similarity 167 member A [Source:HGNC Symbol;Acc:HGNC:15549]"}, {"versioned_ensembl_gene_id":"ENSG00000255020.1","gene_symbol":"AF131216.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11345748,"end":11347502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280182.1","gene_symbol":"AC131888.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81261924,"end":81264091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135697.9","gene_symbol":"BCO1","gene_name":"beta-carotene oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:13815]","synonyms":"FLJ10730,BCMO1,BCMO,BCDO1,BCDO","biotype":"protein_coding","ncbi_id":"53630","summary":"Vitamin A metabolism is important for vital processes such as vision, embryonic development, cell differentiation, and membrane and skin protection. The protein encoded by this gene is a key enzyme in beta-carotene metabolism to vitamin A. It catalyzes the oxidative cleavage of beta,beta-carotene into two retinal molecules. [provided by RefSeq, Jul 2008]","start":81238448,"end":81291142,"strand":1,"description":"beta-carotene oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:13815]"}, {"versioned_ensembl_gene_id":"ENSG00000031698.12","gene_symbol":"SARS","gene_name":"seryl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:10537]","synonyms":"SERS","biotype":"protein_coding","ncbi_id":"6301","summary":"This gene belongs to the class II amino-acyl tRNA family. The encoded enzyme catalyzes the transfer of L-serine to tRNA (Ser) and is related to bacterial and yeast counterparts. Multiple alternatively spliced transcript variants have been described but the biological validity of all variants is unknown. [provided by RefSeq, Jul 2010]","start":109213918,"end":109238169,"strand":1,"description":"seryl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:10537]"}, {"versioned_ensembl_gene_id":"ENSG00000258443.1","gene_symbol":"AC005225.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73517233,"end":73520648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250170.1","gene_symbol":"RASA2-IT1","gene_name":"RASA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41376]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874298","summary":null,"start":141525133,"end":141526121,"strand":1,"description":"RASA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41376]"}, {"versioned_ensembl_gene_id":"ENSG00000018869.16","gene_symbol":"ZNF582","gene_name":"zinc finger protein 582 [Source:HGNC Symbol;Acc:HGNC:26421]","synonyms":"FLJ30927","biotype":"protein_coding","ncbi_id":"147948","summary":"The protein encoded by this gene is a zing finger protein and putative transcription factor that is highly methylated in cervical cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":56375846,"end":56393545,"strand":-1,"description":"zinc finger protein 582 [Source:HGNC Symbol;Acc:HGNC:26421]"}, {"versioned_ensembl_gene_id":"ENSG00000185031.6","gene_symbol":"SLC2A3P2","gene_name":"solute carrier family 2 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31074]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391045","summary":null,"start":64984608,"end":64986087,"strand":-1,"description":"solute carrier family 2 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31074]"}, {"versioned_ensembl_gene_id":"ENSG00000184227.7","gene_symbol":"ACOT1","gene_name":"acyl-CoA thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:33128]","synonyms":"CTE-1,ACH2,LACH2","biotype":"protein_coding","ncbi_id":"641371","summary":null,"start":73537114,"end":73543794,"strand":1,"description":"acyl-CoA thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:33128]"}, {"versioned_ensembl_gene_id":"ENSG00000158079.14","gene_symbol":"PTPDC1","gene_name":"protein tyrosine phosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30184]","synonyms":"PTP9Q22,FLJ37312","biotype":"protein_coding","ncbi_id":"138639","summary":"The protein encoded by this gene contains a characteristic motif of protein tyrosine phosphatases (PTPs). PTPs regulate activities of phosphoproteins through dephosphorylation. They are signaling molecules involved in the regulation of a wide variety of biological processes. The specific function of this protein has not yet been determined. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":94030794,"end":94109856,"strand":1,"description":"protein tyrosine phosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30184]"}, {"versioned_ensembl_gene_id":"ENSG00000255224.1","gene_symbol":"AC109322.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144078002,"end":144079265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263146.2","gene_symbol":"LINC01896","gene_name":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645321","summary":null,"start":78976555,"end":78979074,"strand":-1,"description":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]"}, {"versioned_ensembl_gene_id":"ENSG00000017427.15","gene_symbol":"IGF1","gene_name":"insulin like growth factor 1 [Source:HGNC Symbol;Acc:HGNC:5464]","synonyms":"IGFI,IGF1A,IGF-I","biotype":"protein_coding","ncbi_id":"3479","summary":"The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]","start":102395867,"end":102480645,"strand":-1,"description":"insulin like growth factor 1 [Source:HGNC Symbol;Acc:HGNC:5464]"}, {"versioned_ensembl_gene_id":"ENSG00000265101.1","gene_symbol":"AC091027.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78925064,"end":78927441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283052.1","gene_symbol":"LINC02456","gene_name":"long intergenic non-protein coding RNA 2456 [Source:HGNC Symbol;Acc:HGNC:53389]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369942","summary":null,"start":102304355,"end":102463491,"strand":1,"description":"long intergenic non-protein coding RNA 2456 [Source:HGNC Symbol;Acc:HGNC:53389]"}, {"versioned_ensembl_gene_id":"ENSG00000211626.2","gene_symbol":"IGKV6D-41","gene_name":"immunoglobulin kappa variable 6D-41 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5838]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28869","summary":null,"start":90069662,"end":90070238,"strand":1,"description":"immunoglobulin kappa variable 6D-41 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5838]"}, {"versioned_ensembl_gene_id":"ENSG00000279945.1","gene_symbol":"AC013489.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88477871,"end":88478387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242766.1","gene_symbol":"IGKV1D-17","gene_name":"immunoglobulin kappa variable 1D-17 [Source:HGNC Symbol;Acc:HGNC:5749]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28900","summary":null,"start":90082635,"end":90083291,"strand":1,"description":"immunoglobulin kappa variable 1D-17 [Source:HGNC Symbol;Acc:HGNC:5749]"}, {"versioned_ensembl_gene_id":"ENSG00000267710.6","gene_symbol":"EDDM13","gene_name":"epididymal protein 13 [Source:HGNC Symbol;Acc:HGNC:53168]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506374","summary":null,"start":56272769,"end":56310450,"strand":1,"description":"epididymal protein 13 [Source:HGNC Symbol;Acc:HGNC:53168]"}, {"versioned_ensembl_gene_id":"ENSG00000267776.1","gene_symbol":"AC006116.10","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56376704,"end":56377284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151490.13","gene_symbol":"PTPRO","gene_name":"protein tyrosine phosphatase, receptor type O [Source:HGNC Symbol;Acc:HGNC:9678]","synonyms":"PTPU2,PTP-U2,PTP-oc,NPHS6,GLEPP1","biotype":"protein_coding","ncbi_id":"5800","summary":"This gene encodes a member of the R3 subtype family of receptor-type protein tyrosine phosphatases. These proteins are localized to the apical surface of polarized cells and may have tissue-specific functions through activation of Src family kinases. This gene contains two distinct promoters, and alternatively spliced transcript variants encoding multiple isoforms have been observed. The encoded proteins may have multiple isoform-specific and tissue-specific functions, including the regulation of osteoclast production and activity, inhibition of cell proliferation and facilitation of apoptosis. This gene is a candidate tumor suppressor, and decreased expression of this gene has been observed in several types of cancer. [provided by RefSeq, May 2011]","start":15322397,"end":15597399,"strand":1,"description":"protein tyrosine phosphatase, receptor type O [Source:HGNC Symbol;Acc:HGNC:9678]"}, {"versioned_ensembl_gene_id":"ENSG00000255547.1","gene_symbol":"RPA2P3","gene_name":"replication protein A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420359","summary":null,"start":100336856,"end":100337625,"strand":1,"description":"replication protein A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45118]"}, {"versioned_ensembl_gene_id":"ENSG00000265574.1","gene_symbol":"WDR45BP1","gene_name":"WD repeat domain 45B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26605]","synonyms":"WDR45LP1","biotype":"processed_pseudogene","ncbi_id":"646086","summary":null,"start":32111562,"end":32112590,"strand":-1,"description":"WD repeat domain 45B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26605]"}, {"versioned_ensembl_gene_id":"ENSG00000161265.14","gene_symbol":"U2AF1L4","gene_name":"U2 small nuclear RNA auxiliary factor 1 like 4 [Source:HGNC Symbol;Acc:HGNC:23020]","synonyms":"U2af26,U2AF1L3,MGC33901","biotype":"protein_coding","ncbi_id":"199746","summary":null,"start":35742464,"end":35745445,"strand":-1,"description":"U2 small nuclear RNA auxiliary factor 1 like 4 [Source:HGNC Symbol;Acc:HGNC:23020]"}, {"versioned_ensembl_gene_id":"ENSG00000166159.10","gene_symbol":"LRTM2","gene_name":"leucine rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:32443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654429","summary":null,"start":1820267,"end":1836752,"strand":1,"description":"leucine rich repeats and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:32443]"}, {"versioned_ensembl_gene_id":"ENSG00000242290.2","gene_symbol":"ZBTB20-AS5","gene_name":"ZBTB20 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:52841]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929754","summary":null,"start":114445521,"end":114529452,"strand":1,"description":"ZBTB20 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:52841]"}, {"versioned_ensembl_gene_id":"ENSG00000229774.1","gene_symbol":"AC018866.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120686635,"end":120710517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226550.1","gene_symbol":"CR759848.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32751146,"end":32751980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008056.13","gene_symbol":"SYN1","gene_name":"synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6853","summary":"This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":47571898,"end":47619943,"strand":-1,"description":"synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]"}, {"versioned_ensembl_gene_id":"ENSG00000241295.1","gene_symbol":"ZBTB20-AS2","gene_name":"ZBTB20 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42421]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506673","summary":null,"start":114684580,"end":114687609,"strand":1,"description":"ZBTB20 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42421]"}, {"versioned_ensembl_gene_id":"ENSG00000187688.14","gene_symbol":"TRPV2","gene_name":"transient receptor potential cation channel subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:18082]","synonyms":"VRL1,VRL-1,VRL","biotype":"protein_coding","ncbi_id":"51393","summary":"This gene encodes an ion channel that is activated by high temperatures above 52 degrees Celsius. The protein may be involved in transduction of high-temperature heat responses in sensory ganglia. It is thought that in other tissues the channel may be activated by stimuli other than heat. [provided by RefSeq, Jul 2008]","start":16415542,"end":16437003,"strand":1,"description":"transient receptor potential cation channel subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:18082]"}, {"versioned_ensembl_gene_id":"ENSG00000228025.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32739769,"end":32740601,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000216360.1","gene_symbol":"AL136968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5817421,"end":5818366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264739.1","gene_symbol":"AC093484.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16414524,"end":16416689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170468.7","gene_symbol":"RIOX1","gene_name":"ribosomal oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:20968]","synonyms":"NO66,MAPJD,JMJD9,FLJ21802,C14orf169","biotype":"protein_coding","ncbi_id":"79697","summary":null,"start":73490964,"end":73493392,"strand":1,"description":"ribosomal oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:20968]"}, {"versioned_ensembl_gene_id":"ENSG00000081760.16","gene_symbol":"AACS","gene_name":"acetoacetyl-CoA synthetase [Source:HGNC Symbol;Acc:HGNC:21298]","synonyms":"SUR-5,FLJ12389,ACSF1","biotype":"protein_coding","ncbi_id":"65985","summary":null,"start":125065379,"end":125143333,"strand":1,"description":"acetoacetyl-CoA synthetase [Source:HGNC Symbol;Acc:HGNC:21298]"}, {"versioned_ensembl_gene_id":"ENSG00000267439.1","gene_symbol":"AD000671.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35747057,"end":35753415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214823.3","gene_symbol":"NXT1P1","gene_name":"nuclear transport factor 2 like export factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652801","summary":null,"start":39169636,"end":39169951,"strand":-1,"description":"nuclear transport factor 2 like export factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39708]"}, {"versioned_ensembl_gene_id":"ENSG00000229255.1","gene_symbol":"AC138089.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":248484245,"end":248485484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257142.1","gene_symbol":"AL512310.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19700479,"end":19700650,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196539.3","gene_symbol":"OR2T3","gene_name":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343173","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248473351,"end":248474307,"strand":1,"description":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]"}, {"versioned_ensembl_gene_id":"ENSG00000112039.3","gene_symbol":"FANCE","gene_name":"Fanconi anemia complementation group E [Source:HGNC Symbol;Acc:HGNC:3586]","synonyms":"FAE,FACE","biotype":"protein_coding","ncbi_id":"2178","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group E. [provided by RefSeq, Jul 2008]","start":35452361,"end":35467103,"strand":1,"description":"Fanconi anemia complementation group E [Source:HGNC Symbol;Acc:HGNC:3586]"}, {"versioned_ensembl_gene_id":"ENSG00000258623.1","gene_symbol":"AL121820.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68683411,"end":68685565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241945.7","gene_symbol":"PWP2","gene_name":"PWP2, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:9711]","synonyms":"EHOC-17,UTP1,PWP2H","biotype":"protein_coding","ncbi_id":"5822","summary":null,"start":44107290,"end":44131181,"strand":1,"description":"PWP2, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:9711]"}, {"versioned_ensembl_gene_id":"ENSG00000274696.2","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724453,"end":54767462,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000162551.13","gene_symbol":"ALPL","gene_name":"alkaline phosphatase, liver/bone/kidney [Source:HGNC Symbol;Acc:HGNC:438]","synonyms":"TNSALP,HOPS","biotype":"protein_coding","ncbi_id":"249","summary":"This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015]","start":21509372,"end":21578412,"strand":1,"description":"alkaline phosphatase, liver/bone/kidney [Source:HGNC Symbol;Acc:HGNC:438]"}, {"versioned_ensembl_gene_id":"ENSG00000274851.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754976,"end":54767325,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000253605.1","gene_symbol":"HNRNPA1P38","gene_name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421384","summary":null,"start":141459075,"end":141460031,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]"}, {"versioned_ensembl_gene_id":"ENSG00000213924.3","gene_symbol":"HNRNPH1P2","gene_name":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129368","summary":null,"start":143677153,"end":143678362,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48810]"}, {"versioned_ensembl_gene_id":"ENSG00000253388.1","gene_symbol":"AC124067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37480089,"end":37480809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254294.1","gene_symbol":"AC021305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123400582,"end":123402095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230750.1","gene_symbol":"SDAD1P2","gene_name":"SDA1 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400836","summary":null,"start":10385779,"end":10387806,"strand":1,"description":"SDA1 domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31404]"}, {"versioned_ensembl_gene_id":"ENSG00000253365.1","gene_symbol":"IGKV1D-22","gene_name":"immunoglobulin kappa variable 1D-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5750]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28899","summary":null,"start":90010741,"end":90011184,"strand":1,"description":"immunoglobulin kappa variable 1D-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5750]"}, {"versioned_ensembl_gene_id":"ENSG00000257698.1","gene_symbol":"AC084033.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57931528,"end":57936175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228718.1","gene_symbol":"LINC02521","gene_name":"long intergenic non-protein coding RNA 2521 [Source:HGNC Symbol;Acc:HGNC:53560]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374885","summary":null,"start":2636936,"end":2640001,"strand":1,"description":"long intergenic non-protein coding RNA 2521 [Source:HGNC Symbol;Acc:HGNC:53560]"}, {"versioned_ensembl_gene_id":"ENSG00000253414.2","gene_symbol":"AC124067.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37516410,"end":37517021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103485.17","gene_symbol":"QPRT","gene_name":"quinolinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:9755]","synonyms":"QPRTase","biotype":"protein_coding","ncbi_id":"23475","summary":"This gene encodes a key enzyme in catabolism of quinolinate, an intermediate in the tryptophan-nicotinamide adenine dinucleotide pathway. Quinolinate acts as a most potent endogenous exitotoxin to neurons. Elevation of quinolinate levels in the brain has been linked to the pathogenesis of neurodegenerative disorders such as epilepsy, Alzheimer's disease, and Huntington's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":29679008,"end":29698699,"strand":1,"description":"quinolinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:9755]"}, {"versioned_ensembl_gene_id":"ENSG00000231823.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32895064,"end":32900625,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000131848.9","gene_symbol":"ZSCAN5A","gene_name":"zinc finger and SCAN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:23710]","synonyms":"ZSCAN5,ZNF495,MGC4161","biotype":"protein_coding","ncbi_id":"79149","summary":null,"start":56219670,"end":56368383,"strand":-1,"description":"zinc finger and SCAN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:23710]"}, {"versioned_ensembl_gene_id":"ENSG00000242767.1","gene_symbol":"ZBTB20-AS4","gene_name":"ZBTB20 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42423]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874131","summary":null,"start":115100423,"end":115103061,"strand":1,"description":"ZBTB20 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42423]"}, {"versioned_ensembl_gene_id":"ENSG00000213014.3","gene_symbol":"VN2R17P","gene_name":"vomeronasal 2 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:33223]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649186","summary":null,"start":56317177,"end":56318008,"strand":-1,"description":"vomeronasal 2 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:33223]"}, {"versioned_ensembl_gene_id":"ENSG00000282749.1","gene_symbol":"AC006449.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38550147,"end":38552244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265944.1","gene_symbol":"LINC01387","gene_name":"long intergenic non-protein coding RNA 1387 [Source:HGNC Symbol;Acc:HGNC:44660]","synonyms":"C18orf64","biotype":"lincRNA","ncbi_id":"100130480","summary":null,"start":6511416,"end":6590653,"strand":1,"description":"long intergenic non-protein coding RNA 1387 [Source:HGNC Symbol;Acc:HGNC:44660]"}, {"versioned_ensembl_gene_id":"ENSG00000120279.6","gene_symbol":"MYCT1","gene_name":"MYC target 1 [Source:HGNC Symbol;Acc:HGNC:23172]","synonyms":"MTLC,FLJ21269","biotype":"protein_coding","ncbi_id":"80177","summary":null,"start":152697895,"end":152724567,"strand":1,"description":"MYC target 1 [Source:HGNC Symbol;Acc:HGNC:23172]"}, {"versioned_ensembl_gene_id":"ENSG00000253730.1","gene_symbol":"AC015909.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50158333,"end":50161276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176476.8","gene_symbol":"SGF29","gene_name":"SAGA complex associated factor 29 [Source:HGNC Symbol;Acc:HGNC:25156]","synonyms":"TDRD29,FLJ32446,CCDC101","biotype":"protein_coding","ncbi_id":"112869","summary":"CCDC101 is a subunit of 2 histone acetyltransferase complexes: the ADA2A (TADA2A; MIM 602276)-containing (ATAC) complex and the SPT3 (SUPT3H; MIM 602947)-TAF9 (MIM 600822)-GCN5 (KAT2A; MIM 602301)/PCAF (KAT2B; MIM 602303) acetylase (STAGA) complex. Both of these complexes contain either GCN5 or PCAF, which are paralogous acetyltransferases (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010]","start":28553915,"end":28591790,"strand":1,"description":"SAGA complex associated factor 29 [Source:HGNC Symbol;Acc:HGNC:25156]"}, {"versioned_ensembl_gene_id":"ENSG00000226205.1","gene_symbol":"AC007790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133732493,"end":133733595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235967.1","gene_symbol":"COX5BP3","gene_name":"cytochrome c oxidase subunit 5B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2272]","synonyms":"COX5BL3","biotype":"processed_pseudogene","ncbi_id":"1332","summary":null,"start":133727368,"end":133727734,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:2272]"}, {"versioned_ensembl_gene_id":"ENSG00000277621.1","gene_symbol":"AC005277.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12982613,"end":12983002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077463.14","gene_symbol":"SIRT6","gene_name":"sirtuin 6 [Source:HGNC Symbol;Acc:HGNC:14934]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51548","summary":"This gene encodes a member of the sirtuin family of NAD-dependent enzymes that are implicated in cellular stress resistance, genomic stability, aging and energy homeostasis. The encoded protein is localized to the nucleus, exhibits ADP-ribosyl transferase and histone deacetylase activities, and plays a role in DNA repair, maintenance of telomeric chromatin, inflammation, lipid and glucose metabolism. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":4174109,"end":4182604,"strand":-1,"description":"sirtuin 6 [Source:HGNC Symbol;Acc:HGNC:14934]"}, {"versioned_ensembl_gene_id":"ENSG00000248854.1","gene_symbol":"HNRNPH1P3","gene_name":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402216","summary":null,"start":55838801,"end":55840025,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48811]"}, {"versioned_ensembl_gene_id":"ENSG00000198155.5","gene_symbol":"ZNF876P","gene_name":"zinc finger protein 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:32472]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"642280","summary":null,"start":212610,"end":255985,"strand":1,"description":"zinc finger protein 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:32472]"}, {"versioned_ensembl_gene_id":"ENSG00000255039.1","gene_symbol":"LINC02553","gene_name":"long intergenic non-protein coding RNA 2553 [Source:HGNC Symbol;Acc:HGNC:53588]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369449","summary":null,"start":97222644,"end":97259987,"strand":-1,"description":"long intergenic non-protein coding RNA 2553 [Source:HGNC Symbol;Acc:HGNC:53588]"}, {"versioned_ensembl_gene_id":"ENSG00000198128.4","gene_symbol":"OR2L3","gene_name":"olfactory receptor family 2 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:15009]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391192","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248046836,"end":248063407,"strand":1,"description":"olfactory receptor family 2 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:15009]"}, {"versioned_ensembl_gene_id":"ENSG00000107566.13","gene_symbol":"ERLIN1","gene_name":"ER lipid raft associated 1 [Source:HGNC Symbol;Acc:HGNC:16947]","synonyms":"SPG62,SPFH1,KE04,Erlin-1,C10orf69","biotype":"protein_coding","ncbi_id":"10613","summary":"The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62. [provided by RefSeq, Dec 2016]","start":100150094,"end":100188334,"strand":-1,"description":"ER lipid raft associated 1 [Source:HGNC Symbol;Acc:HGNC:16947]"}, {"versioned_ensembl_gene_id":"ENSG00000128655.17","gene_symbol":"PDE11A","gene_name":"phosphodiesterase 11A [Source:HGNC Symbol;Acc:HGNC:8773]","synonyms":"PPNAD2","biotype":"protein_coding","ncbi_id":"50940","summary":"The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a member of the PDE protein superfamily. Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":177623252,"end":178072755,"strand":-1,"description":"phosphodiesterase 11A [Source:HGNC Symbol;Acc:HGNC:8773]"}, {"versioned_ensembl_gene_id":"ENSG00000067704.9","gene_symbol":"IARS2","gene_name":"isoleucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29685]","synonyms":"FLJ10326","biotype":"protein_coding","ncbi_id":"55699","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Two forms of isoleucine-tRNA synthetase exist, a cytoplasmic form and a mitochondrial form. This gene encodes the mitochondrial isoleucine-tRNA synthetase which belongs to the class-I aminoacyl-tRNA synthetase family. [provided by RefSeq, Dec 2014]","start":220094102,"end":220148041,"strand":1,"description":"isoleucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29685]"}, {"versioned_ensembl_gene_id":"ENSG00000232134.1","gene_symbol":"RPS15AP12","gene_name":"ribosomal protein S15a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129243","summary":null,"start":220143964,"end":220144351,"strand":-1,"description":"ribosomal protein S15a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36759]"}, {"versioned_ensembl_gene_id":"ENSG00000146707.14","gene_symbol":"POMZP3","gene_name":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]","synonyms":"POM121,POM-ZP3","biotype":"protein_coding","ncbi_id":"22932","summary":"This gene appears to have resulted from a fusion of DNA sequences derived from 2 distinct loci, specifically through the duplication of two internal exons from the POM121 gene and four 3' exons from the ZP3 gene. The 5' end of this gene is similar to the 5` coding region of the POM121 gene which encodes an integral nuclear pore membrane protein. However, the protein encoded by this gene lacks the nuclear pore localization motif. The 3' end of this gene is similar to the last 4 exons of the zona pellucida glycoprotein 3 (ZP3) gene and the encoded protein retains one zona pellucida domain. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":76609986,"end":76627261,"strand":-1,"description":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]"}, {"versioned_ensembl_gene_id":"ENSG00000197454.2","gene_symbol":"OR2L5","gene_name":"olfactory receptor family 2 subfamily L member 5 [Source:HGNC Symbol;Acc:HGNC:15011]","synonyms":"OR2L5P,OR2L11","biotype":"protein_coding","ncbi_id":"81466","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248013660,"end":248024276,"strand":1,"description":"olfactory receptor family 2 subfamily L member 5 [Source:HGNC Symbol;Acc:HGNC:15011]"}, {"versioned_ensembl_gene_id":"ENSG00000261198.1","gene_symbol":"AC005774.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7614230,"end":7614992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282579.1","gene_symbol":"IGHV4-39","gene_name":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28394","summary":null,"start":106446390,"end":106446899,"strand":-1,"description":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]"}, {"versioned_ensembl_gene_id":"ENSG00000081800.8","gene_symbol":"SLC13A1","gene_name":"solute carrier family 13 member 1 [Source:HGNC Symbol;Acc:HGNC:10916]","synonyms":"NaSi-1,NAS1","biotype":"protein_coding","ncbi_id":"6561","summary":"The protein encoded by this gene is an apical membrane Na(+)-sulfate cotransporter involved in sulfate homeostasis in the kidney. Defects in this gene lead to many pathophysiologic problems. [provided by RefSeq, May 2016]","start":123113531,"end":123199986,"strand":-1,"description":"solute carrier family 13 member 1 [Source:HGNC Symbol;Acc:HGNC:10916]"}, {"versioned_ensembl_gene_id":"ENSG00000280224.1","gene_symbol":"AL008636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49500568,"end":49501585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212939.2","gene_symbol":"Z97192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49548681,"end":49556473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270001.1","gene_symbol":"AL121894.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23631826,"end":23632316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263353.3","gene_symbol":"PPIAL4A","gene_name":"peptidylprolyl isomerase A like 4A [Source:HGNC Symbol;Acc:HGNC:24369]","synonyms":"PPIAL4B,PPIAL4,COAS2","biotype":"protein_coding","ncbi_id":"653505","summary":null,"start":120889746,"end":120890405,"strand":1,"description":"peptidylprolyl isomerase A like 4A [Source:HGNC Symbol;Acc:HGNC:24369]"}, {"versioned_ensembl_gene_id":"ENSG00000226121.2","gene_symbol":"AC009487.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161500885,"end":161507705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184384.13","gene_symbol":"MAML2","gene_name":"mastermind like transcriptional coactivator 2 [Source:HGNC Symbol;Acc:HGNC:16259]","synonyms":"MAM3,KIAA1819","biotype":"protein_coding","ncbi_id":"84441","summary":"The protein encoded by this gene is a member of the Mastermind-like family of proteins. All family members are proline and glutamine-rich, and contain a conserved basic domain that binds the ankyrin repeat domain of the intracellular domain of the Notch receptors (ICN1-4) in their N-terminus, and a transcriptional activation domain in their C-terminus. This protein binds to an extended groove that is formed by the interaction of CBF1, Suppressor of Hairless, LAG-1 (CSL) with ICN, and positively regulates Notch signaling. High levels of expression of this gene have been observed in several B cell-derived lymphomas. Translocations resulting in fusion proteins with both CRTC1 and CRTC3 have been implicated in the development of mucoepidermoid carcinomas, while a translocation event with CXCR4 has been linked with chronic lymphocytic leukemia (CLL). Copy number variation in the polyglutamine tract has been observed. [provided by RefSeq, Jan 2015]","start":95976598,"end":96343180,"strand":-1,"description":"mastermind like transcriptional coactivator 2 [Source:HGNC Symbol;Acc:HGNC:16259]"}, {"versioned_ensembl_gene_id":"ENSG00000249047.2","gene_symbol":"COX6B1P5","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37675]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289662","summary":null,"start":2234251,"end":2234499,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37675]"}, {"versioned_ensembl_gene_id":"ENSG00000230576.1","gene_symbol":"OR6R1P","gene_name":"olfactory receptor family 6 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15037]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81440","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247833349,"end":247834288,"strand":-1,"description":"olfactory receptor family 6 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15037]"}, {"versioned_ensembl_gene_id":"ENSG00000228336.2","gene_symbol":"OR9H1P","gene_name":"olfactory receptor family 9 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15038]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"81439","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247770169,"end":247779524,"strand":1,"description":"olfactory receptor family 9 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15038]"}, {"versioned_ensembl_gene_id":"ENSG00000221888.4","gene_symbol":"OR1C1","gene_name":"olfactory receptor family 1 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8182]","synonyms":"TPCR27,HSTPCR27","biotype":"protein_coding","ncbi_id":"26188","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247754846,"end":247760556,"strand":-1,"description":"olfactory receptor family 1 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8182]"}, {"versioned_ensembl_gene_id":"ENSG00000220184.2","gene_symbol":"HMGB3P18","gene_name":"high mobility group box 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39310]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644502","summary":null,"start":121858179,"end":121858768,"strand":-1,"description":"high mobility group box 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39310]"}, {"versioned_ensembl_gene_id":"ENSG00000162959.13","gene_symbol":"MEMO1","gene_name":"mediator of cell motility 1 [Source:HGNC Symbol;Acc:HGNC:14014]","synonyms":"MEMO,CGI-27,C2orf4","biotype":"protein_coding","ncbi_id":"51072","summary":null,"start":31865060,"end":32011230,"strand":-1,"description":"mediator of cell motility 1 [Source:HGNC Symbol;Acc:HGNC:14014]"}, {"versioned_ensembl_gene_id":"ENSG00000271317.1","gene_symbol":"IGHD4OR15-4A","gene_name":"immunoglobulin heavy diversity 4/OR15-4A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5506]","synonyms":"IGHD4OR154A,IGHD4/OR15-4A","biotype":"IG_D_gene","ncbi_id":"28329","summary":null,"start":20004797,"end":20004815,"strand":-1,"description":"immunoglobulin heavy diversity 4/OR15-4A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5506]"}, {"versioned_ensembl_gene_id":"ENSG00000214628.3","gene_symbol":"NDUFB5P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52268]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422431","summary":null,"start":96953630,"end":96954195,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52268]"}, {"versioned_ensembl_gene_id":"ENSG00000198445.4","gene_symbol":"CCT8L2","gene_name":"chaperonin containing TCP1 subunit 8 like 2 [Source:HGNC Symbol;Acc:HGNC:15553]","synonyms":"CESK1","biotype":"protein_coding","ncbi_id":"150160","summary":null,"start":16590751,"end":16592810,"strand":-1,"description":"chaperonin containing TCP1 subunit 8 like 2 [Source:HGNC Symbol;Acc:HGNC:15553]"}, {"versioned_ensembl_gene_id":"ENSG00000239435.2","gene_symbol":"KCNMB3P1","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6288]","synonyms":"KCNMBLP,KCNMB3L1,KCNMB3L,KCNMB2L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"27093","summary":null,"start":16575363,"end":16582707,"strand":-1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6288]"}, {"versioned_ensembl_gene_id":"ENSG00000259490.2","gene_symbol":"IGHV3OR15-7","gene_name":"immunoglobulin heavy variable 3/OR15-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5633]","synonyms":"IGHV3/OR15-7","biotype":"IG_V_gene","ncbi_id":"28318","summary":null,"start":19987656,"end":19988117,"strand":-1,"description":"immunoglobulin heavy variable 3/OR15-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5633]"}, {"versioned_ensembl_gene_id":"ENSG00000266158.2","gene_symbol":"RN7SL785P","gene_name":"RNA, 7SL, cytoplasmic 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:46801]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480532","summary":null,"start":47280811,"end":47281063,"strand":-1,"description":"RNA, 7SL, cytoplasmic 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:46801]"}, {"versioned_ensembl_gene_id":"ENSG00000259337.4","gene_symbol":"IGHV1OR15-2","gene_name":"immunoglobulin heavy variable 1/OR15-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5564]","synonyms":"IGHV1/OR15-2","biotype":"IG_V_pseudogene","ncbi_id":"100287128","summary":null,"start":19972782,"end":19973218,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5564]"}, {"versioned_ensembl_gene_id":"ENSG00000171729.13","gene_symbol":"TMEM51","gene_name":"transmembrane protein 51 [Source:HGNC Symbol;Acc:HGNC:25488]","synonyms":"FLJ10199,C1orf72","biotype":"protein_coding","ncbi_id":"55092","summary":null,"start":15152532,"end":15220480,"strand":1,"description":"transmembrane protein 51 [Source:HGNC Symbol;Acc:HGNC:25488]"}, {"versioned_ensembl_gene_id":"ENSG00000163040.14","gene_symbol":"CCDC74A","gene_name":"coiled-coil domain containing 74A [Source:HGNC Symbol;Acc:HGNC:25197]","synonyms":"FLJ40345","biotype":"protein_coding","ncbi_id":"90557","summary":null,"start":131527675,"end":131533666,"strand":1,"description":"coiled-coil domain containing 74A [Source:HGNC Symbol;Acc:HGNC:25197]"}, {"versioned_ensembl_gene_id":"ENSG00000204464.7","gene_symbol":"C1orf195","gene_name":"chromosome 1 open reading frame 195 [Source:HGNC Symbol;Acc:HGNC:32332]","synonyms":null,"biotype":"lincRNA","ncbi_id":"727684","summary":null,"start":15164344,"end":15171317,"strand":-1,"description":"chromosome 1 open reading frame 195 [Source:HGNC Symbol;Acc:HGNC:32332]"}, {"versioned_ensembl_gene_id":"ENSG00000215720.4","gene_symbol":"AL035405.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15191828,"end":15192845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273391.1","gene_symbol":"AC083880.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139359032,"end":139359566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279388.1","gene_symbol":"AC073578.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131478844,"end":131483034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242070.1","gene_symbol":"NPM1P17","gene_name":"nucleophosmin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:7919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10830","summary":null,"start":137723774,"end":137724543,"strand":1,"description":"nucleophosmin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:7919]"}, {"versioned_ensembl_gene_id":"ENSG00000256209.1","gene_symbol":"AC073578.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131469311,"end":131492951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206013.2","gene_symbol":"IFITM5","gene_name":"interferon induced transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:16644]","synonyms":"BRIL,Hrmp1,fragilis4","biotype":"protein_coding","ncbi_id":"387733","summary":"This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012]","start":298200,"end":299526,"strand":-1,"description":"interferon induced transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:16644]"}, {"versioned_ensembl_gene_id":"ENSG00000280409.1","gene_symbol":"LINC01101","gene_name":"long intergenic non-protein coding RNA 1101 [Source:HGNC Symbol;Acc:HGNC:25923]","synonyms":"FLJ14816","biotype":"TEC","ncbi_id":"84931","summary":null,"start":120464335,"end":120466218,"strand":-1,"description":"long intergenic non-protein coding RNA 1101 [Source:HGNC Symbol;Acc:HGNC:25923]"}, {"versioned_ensembl_gene_id":"ENSG00000026508.17","gene_symbol":"CD44","gene_name":"CD44 molecule (Indian blood group) [Source:HGNC Symbol;Acc:HGNC:1681]","synonyms":"MIC4,MDU3,MDU2,MC56,IN,HCELL,CSPG8,CD44R,Pgp1","biotype":"protein_coding","ncbi_id":"960","summary":"The protein encoded by this gene is a cell-surface glycoprotein involved in cell-cell interactions, cell adhesion and migration. It is a receptor for hyaluronic acid (HA) and can also interact with other ligands, such as osteopontin, collagens, and matrix metalloproteinases (MMPs). This protein participates in a wide variety of cellular functions including lymphocyte activation, recirculation and homing, hematopoiesis, and tumor metastasis. Transcripts for this gene undergo complex alternative splicing that results in many functionally distinct isoforms, however, the full length nature of some of these variants has not been determined. Alternative splicing is the basis for the structural and functional diversity of this protein, and may be related to tumor metastasis. [provided by RefSeq, Jul 2008]","start":35138870,"end":35232402,"strand":1,"description":"CD44 molecule (Indian blood group) [Source:HGNC Symbol;Acc:HGNC:1681]"}, {"versioned_ensembl_gene_id":"ENSG00000234041.1","gene_symbol":"AL512326.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179137764,"end":179137934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282595.1","gene_symbol":"AC234301.4","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106380821,"end":106381287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278082.3","gene_symbol":"AC234301.1","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106373990,"end":106374420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243430.1","gene_symbol":"CR788234.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29742604,"end":29746182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257162.6","gene_symbol":"MED15P6","gene_name":"mediator complex subunit 15 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48655]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100996438","summary":null,"start":19485336,"end":19489148,"strand":1,"description":"mediator complex subunit 15 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48655]"}, {"versioned_ensembl_gene_id":"ENSG00000227484.1","gene_symbol":"CR559946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50314631,"end":50316008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248703.2","gene_symbol":"LINC02415","gene_name":"long intergenic non-protein coding RNA 2415 [Source:HGNC Symbol;Acc:HGNC:53344]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107161159","summary":null,"start":131296110,"end":131297972,"strand":-1,"description":"long intergenic non-protein coding RNA 2415 [Source:HGNC Symbol;Acc:HGNC:53344]"}, {"versioned_ensembl_gene_id":"ENSG00000261147.1","gene_symbol":"AC091167.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":90249556,"end":90272208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275929.1","gene_symbol":"AC068831.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91031246,"end":91031691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182648.11","gene_symbol":"LINC01006","gene_name":"long intergenic non-protein coding RNA 1006 [Source:HGNC Symbol;Acc:HGNC:48971]","synonyms":"MY040,C7orf13","biotype":"lincRNA","ncbi_id":"100506380","summary":null,"start":156472196,"end":156640654,"strand":-1,"description":"long intergenic non-protein coding RNA 1006 [Source:HGNC Symbol;Acc:HGNC:48971]"}, {"versioned_ensembl_gene_id":"ENSG00000226938.1","gene_symbol":"AC119428.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53348488,"end":53349233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251017.1","gene_symbol":"AC093677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74085995,"end":74086672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050393.11","gene_symbol":"MCUR1","gene_name":"mitochondrial calcium uniporter regulator 1 [Source:HGNC Symbol;Acc:HGNC:21097]","synonyms":"FLJ20958,CCDC90A,C6orf79","biotype":"protein_coding","ncbi_id":"63933","summary":null,"start":13786557,"end":13814568,"strand":-1,"description":"mitochondrial calcium uniporter regulator 1 [Source:HGNC Symbol;Acc:HGNC:21097]"}, {"versioned_ensembl_gene_id":"ENSG00000111802.13","gene_symbol":"TDP2","gene_name":"tyrosyl-DNA phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:17768]","synonyms":"TTRAP","biotype":"protein_coding","ncbi_id":"51567","summary":"This gene encodes a member of a superfamily of divalent cation-dependent phosphodiesterases. The encoded protein associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor associated factors (TRAFs), and inhibits nuclear factor-kappa-B activation. This protein has sequence and structural similarities with APE1 endonuclease, which is involved in both DNA repair and the activation of transcription factors. [provided by RefSeq, Jul 2008]","start":24649977,"end":24667033,"strand":-1,"description":"tyrosyl-DNA phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:17768]"}, {"versioned_ensembl_gene_id":"ENSG00000218891.4","gene_symbol":"ZNF579","gene_name":"zinc finger protein 579 [Source:HGNC Symbol;Acc:HGNC:26646]","synonyms":"FLJ35453","biotype":"protein_coding","ncbi_id":"163033","summary":null,"start":55576770,"end":55580845,"strand":-1,"description":"zinc finger protein 579 [Source:HGNC Symbol;Acc:HGNC:26646]"}, {"versioned_ensembl_gene_id":"ENSG00000150991.14","gene_symbol":"UBC","gene_name":"ubiquitin C [Source:HGNC Symbol;Acc:HGNC:12468]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7316","summary":"This gene represents a ubiquitin gene, ubiquitin C. The encoded protein is a polyubiquitin precursor. Conjugation of ubiquitin monomers or polymers can lead to various effects within a cell, depending on the residues to which ubiquitin is conjugated. Ubiquitination has been associated with protein degradation, DNA repair, cell cycle regulation, kinase modification, endocytosis, and regulation of other cell signaling pathways. [provided by RefSeq, Aug 2010]","start":124911604,"end":124917368,"strand":-1,"description":"ubiquitin C [Source:HGNC Symbol;Acc:HGNC:12468]"}, {"versioned_ensembl_gene_id":"ENSG00000251429.1","gene_symbol":"AC098679.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":158270378,"end":158278676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253925.1","gene_symbol":"AC011369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168085329,"end":168187719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231274.5","gene_symbol":"SBK3","gene_name":"SH3 domain binding kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:44121]","synonyms":"SgK110","biotype":"protein_coding","ncbi_id":"100130827","summary":null,"start":55540656,"end":55545543,"strand":-1,"description":"SH3 domain binding kinase family member 3 [Source:HGNC Symbol;Acc:HGNC:44121]"}, {"versioned_ensembl_gene_id":"ENSG00000176566.4","gene_symbol":"DCAF4L2","gene_name":"DDB1 and CUL4 associated factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:26657]","synonyms":"WDR21C","biotype":"protein_coding","ncbi_id":"138009","summary":null,"start":87870743,"end":87874068,"strand":-1,"description":"DDB1 and CUL4 associated factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:26657]"}, {"versioned_ensembl_gene_id":"ENSG00000181733.3","gene_symbol":"OR2Z1","gene_name":"olfactory receptor family 2 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:15391]","synonyms":"OR2Z2","biotype":"protein_coding","ncbi_id":"284383","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":8721634,"end":8732160,"strand":1,"description":"olfactory receptor family 2 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:15391]"}, {"versioned_ensembl_gene_id":"ENSG00000206492.11","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30530868,"end":30546666,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000230020.1","gene_symbol":"NHS-AS1","gene_name":"NHS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40403]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873920","summary":null,"start":17552349,"end":17557387,"strand":-1,"description":"NHS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40403]"}, {"versioned_ensembl_gene_id":"ENSG00000277252.1","gene_symbol":"AL589743.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19220796,"end":19220912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143971.7","gene_symbol":"ETAA1","gene_name":"ETAA1, ATR kinase activator [Source:HGNC Symbol;Acc:HGNC:24648]","synonyms":"ETAA16","biotype":"protein_coding","ncbi_id":"54465","summary":null,"start":67397319,"end":67410545,"strand":1,"description":"ETAA1, ATR kinase activator [Source:HGNC Symbol;Acc:HGNC:24648]"}, {"versioned_ensembl_gene_id":"ENSG00000144369.12","gene_symbol":"FAM171B","gene_name":"family with sequence similarity 171 member B [Source:HGNC Symbol;Acc:HGNC:29412]","synonyms":"FLJ34104,KIAA1946","biotype":"protein_coding","ncbi_id":"165215","summary":null,"start":186693971,"end":186765965,"strand":1,"description":"family with sequence similarity 171 member B [Source:HGNC Symbol;Acc:HGNC:29412]"}, {"versioned_ensembl_gene_id":"ENSG00000159479.16","gene_symbol":"MED8","gene_name":"mediator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:19971]","synonyms":"MGC19641,MGC17544,ARC32","biotype":"protein_coding","ncbi_id":"112950","summary":"This gene encodes a protein component of the mediator complex, which aids in transcriptional activation through interaction with RNA polymerase II and gene-specific transcription factors. The encoded protein may also function in ubiquitin ligation and protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013]","start":43383917,"end":43389808,"strand":-1,"description":"mediator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:19971]"}, {"versioned_ensembl_gene_id":"ENSG00000223532.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31260536,"end":31347723,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000233231.1","gene_symbol":"HNRNPA1P49","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481663","summary":null,"start":166334568,"end":166335471,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48779]"}, {"versioned_ensembl_gene_id":"ENSG00000276371.2","gene_symbol":"FAM60A","gene_name":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]","synonyms":"TERA,C12orf14","biotype":"protein_coding","ncbi_id":"58516","summary":null,"start":31282857,"end":31329331,"strand":-1,"description":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]"}, {"versioned_ensembl_gene_id":"ENSG00000257691.2","gene_symbol":"AC133555.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29475064,"end":29475355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229890.1","gene_symbol":"ACTP1","gene_name":"actin family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51621]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480335","summary":null,"start":108099110,"end":108099492,"strand":1,"description":"actin family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51621]"}, {"versioned_ensembl_gene_id":"ENSG00000145934.16","gene_symbol":"TENM2","gene_name":"teneurin transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:29943]","synonyms":"Ten-M2,ODZ2,KIAA1127","biotype":"protein_coding","ncbi_id":"57451","summary":null,"start":167284799,"end":168264157,"strand":1,"description":"teneurin transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:29943]"}, {"versioned_ensembl_gene_id":"ENSG00000253660.1","gene_symbol":"AC008464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167937717,"end":167953469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224557.7","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33112451,"end":33129084,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000256056.1","gene_symbol":"AC087257.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27592461,"end":27594039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282378.1","gene_symbol":"AC208188.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":451401,"end":453138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256557.1","gene_symbol":"AC009509.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27608733,"end":27609046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243215.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"RING6,D6S222E","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":33039313,"end":33061428,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000242562.1","gene_symbol":"DCAF13P1","gene_name":"DDB1 and CUL4 associated factor 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129009","summary":null,"start":106125371,"end":106126700,"strand":1,"description":"DDB1 and CUL4 associated factor 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43866]"}, {"versioned_ensembl_gene_id":"ENSG00000136250.11","gene_symbol":"AOAH","gene_name":"acyloxyacyl hydrolase [Source:HGNC Symbol;Acc:HGNC:548]","synonyms":null,"biotype":"protein_coding","ncbi_id":"313","summary":"This locus encodes both the light and heavy subunits of acyloxyacyl hydrolase. The encoded enzyme catalyzes the hydrolysis of acyloxylacyl-linked fatty acyl chains from bacterial lipopolysaccharides, effectively detoxifying these molecules. The encoded protein may play a role in modulating host inflammatory response to gram-negative bacteria. Alternatively spliced transcript variants have been described.[provided by RefSeq, Apr 2010]","start":36512949,"end":36724549,"strand":-1,"description":"acyloxyacyl hydrolase [Source:HGNC Symbol;Acc:HGNC:548]"}, {"versioned_ensembl_gene_id":"ENSG00000262210.1","gene_symbol":"PEBP1P3","gene_name":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129570","summary":null,"start":198690621,"end":198691520,"strand":-1,"description":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]"}, {"versioned_ensembl_gene_id":"ENSG00000187134.13","gene_symbol":"AKR1C1","gene_name":"aldo-keto reductase family 1 member C1 [Source:HGNC Symbol;Acc:HGNC:384]","synonyms":"MBAB,HAKRC,DDH1,DDH,DD1","biotype":"protein_coding","ncbi_id":"1645","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme catalyzes the reaction of progesterone to the inactive form 20-alpha-hydroxy-progesterone. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. [provided by RefSeq, Jul 2008]","start":4963253,"end":4983283,"strand":1,"description":"aldo-keto reductase family 1 member C1 [Source:HGNC Symbol;Acc:HGNC:384]"}, {"versioned_ensembl_gene_id":"ENSG00000280978.1","gene_symbol":"AC106772.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":604294,"end":613884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272599.2","gene_symbol":"AC016394.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73124573,"end":73125532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257987.5","gene_symbol":"TEX49","gene_name":"testis expressed 49 [Source:HGNC Symbol;Acc:HGNC:48628]","synonyms":"LINC00935","biotype":"protein_coding","ncbi_id":"255411","summary":null,"start":48727435,"end":48765786,"strand":1,"description":"testis expressed 49 [Source:HGNC Symbol;Acc:HGNC:48628]"}, {"versioned_ensembl_gene_id":"ENSG00000174450.11","gene_symbol":"GOLGA6L2","gene_name":"golgin A6 family-like 2 [Source:HGNC Symbol;Acc:HGNC:26695]","synonyms":"FLJ36144,CT105","biotype":"protein_coding","ncbi_id":"283685","summary":null,"start":23439498,"end":23447234,"strand":-1,"description":"golgin A6 family-like 2 [Source:HGNC Symbol;Acc:HGNC:26695]"}, {"versioned_ensembl_gene_id":"ENSG00000244550.1","gene_symbol":"AC006455.8","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63233115,"end":63241645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087095.12","gene_symbol":"NLK","gene_name":"nemo like kinase [Source:HGNC Symbol;Acc:HGNC:29858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51701","summary":null,"start":28041737,"end":28196381,"strand":1,"description":"nemo like kinase [Source:HGNC Symbol;Acc:HGNC:29858]"}, {"versioned_ensembl_gene_id":"ENSG00000243302.3","gene_symbol":"AC018638.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128651185,"end":128652334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236957.7","gene_symbol":"AL139010.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157925065,"end":157949071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231389.7","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33064569,"end":33080775,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000146677.7","gene_symbol":"AC004453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44467897,"end":44468304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282072.1","gene_symbol":"AC243657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28904945,"end":28905656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280749.1","gene_symbol":"AC231647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197450327,"end":197456654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138286.14","gene_symbol":"FAM149B1","gene_name":"family with sequence similarity 149 member B1 [Source:HGNC Symbol;Acc:HGNC:29162]","synonyms":"KIAA0974","biotype":"protein_coding","ncbi_id":"317662","summary":null,"start":73168166,"end":73244504,"strand":1,"description":"family with sequence similarity 149 member B1 [Source:HGNC Symbol;Acc:HGNC:29162]"}, {"versioned_ensembl_gene_id":"ENSG00000111215.11","gene_symbol":"PRR4","gene_name":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]","synonyms":"PROL4,LPRP","biotype":"protein_coding","ncbi_id":"11272","summary":"This gene encodes a member of the proline-rich protein family that lacks a conserved repetitive domain. This protein may play a role in protective functions in the eye. Alternative splicing result in multiple transcript variants. Read-through transcription also exists between this gene and the upstream PRH1 (proline-rich protein HaeIII subfamily 1) gene. [provided by RefSeq, Feb 2011]","start":10845849,"end":11171613,"strand":-1,"description":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]"}, {"versioned_ensembl_gene_id":"ENSG00000213126.2","gene_symbol":"AC092642.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179814251,"end":179814675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230392.1","gene_symbol":"AC004835.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119291529,"end":119335610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184708.17","gene_symbol":"EIF4ENIF1","gene_name":"eukaryotic translation initiation factor 4E nuclear import factor 1 [Source:HGNC Symbol;Acc:HGNC:16687]","synonyms":"4E-T,2610509L04Rik,FLJ21601,Clast4","biotype":"protein_coding","ncbi_id":"56478","summary":"The protein encoded by this gene is a nucleocytoplasmic shuttle protein for the translation initiation factor eIF4E. This shuttle protein interacts with the importin alpha-beta complex to mediate nuclear import of eIF4E. It is predominantly cytoplasmic; its own nuclear import is regulated by a nuclear localization signal and nuclear export signals. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":31436977,"end":31496108,"strand":-1,"description":"eukaryotic translation initiation factor 4E nuclear import factor 1 [Source:HGNC Symbol;Acc:HGNC:16687]"}, {"versioned_ensembl_gene_id":"ENSG00000111142.13","gene_symbol":"METAP2","gene_name":"methionyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:16672]","synonyms":"p67,MNPEP,MAP2","biotype":"protein_coding","ncbi_id":"10988","summary":"The protein encoded by this gene is a member of the methionyl aminopeptidase family. The encoded protein functions both by protecting the alpha subunit of eukaryotic initiation factor 2 from inhibitory phosphorylation and by removing the amino-terminal methionine residue from nascent proteins. Increased expression of this gene is associated with various forms of cancer, and the anti-cancer drugs fumagillin and ovalicin inhibit the protein by irreversibly binding to its active site. Inhibitors of this gene have also been shown to be effective for the treatment of obesity. A pseudogene of this gene is located on chromosome 2. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":95473520,"end":95515839,"strand":1,"description":"methionyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:16672]"}, {"versioned_ensembl_gene_id":"ENSG00000283214.1","gene_symbol":"AC006453.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89662601,"end":89662977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226307.1","gene_symbol":"HNRNPDLP1","gene_name":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128595","summary":null,"start":95638375,"end":95638924,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48752]"}, {"versioned_ensembl_gene_id":"ENSG00000282284.1","gene_symbol":"IGHV1-24","gene_name":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28467","summary":null,"start":106277317,"end":106277814,"strand":-1,"description":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]"}, {"versioned_ensembl_gene_id":"ENSG00000229815.1","gene_symbol":"CCNB1IP1P1","gene_name":"cyclin B1 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728887","summary":null,"start":44958557,"end":44959395,"strand":1,"description":"cyclin B1 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37693]"}, {"versioned_ensembl_gene_id":"ENSG00000270601.4","gene_symbol":"PRAMEF5","gene_name":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]","synonyms":"PRAMEF5L,PRAMEF23","biotype":"protein_coding","ncbi_id":"343068","summary":null,"start":13254212,"end":13263314,"strand":1,"description":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]"}, {"versioned_ensembl_gene_id":"ENSG00000232867.1","gene_symbol":"AL355433.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27210327,"end":27210626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249606.1","gene_symbol":"TRAPPC2P7","gene_name":"trafficking protein particle complex 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:10716]","synonyms":"SEDLP7","biotype":"unprocessed_pseudogene","ncbi_id":"392597","summary":null,"start":18655520,"end":18656190,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:10716]"}, {"versioned_ensembl_gene_id":"ENSG00000196406.4","gene_symbol":"SPANXD","gene_name":"SPANX family member D [Source:HGNC Symbol;Acc:HGNC:14332]","synonyms":"CT11.4,SPANXE","biotype":"protein_coding","ncbi_id":"64648","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene encodes a sperm protein that is associated with the nucleus but, although a role in spermatogenesis is suggested, the specific function of this family member has not yet been determined. Polymorphisms in this gene may be associated with prostate cancer susceptibility. [provided by RefSeq, Apr 2014]","start":141697411,"end":141698739,"strand":-1,"description":"SPANX family member D [Source:HGNC Symbol;Acc:HGNC:14332]"}, {"versioned_ensembl_gene_id":"ENSG00000196600.12","gene_symbol":"SLC22A25","gene_name":"solute carrier family 22 member 25 [Source:HGNC Symbol;Acc:HGNC:32935]","synonyms":"UST6,MGC120420,HIMTP","biotype":"protein_coding","ncbi_id":"387601","summary":null,"start":63163776,"end":63229652,"strand":-1,"description":"solute carrier family 22 member 25 [Source:HGNC Symbol;Acc:HGNC:32935]"}, {"versioned_ensembl_gene_id":"ENSG00000146410.11","gene_symbol":"MTFR2","gene_name":"mitochondrial fission regulator 2 [Source:HGNC Symbol;Acc:HGNC:21115]","synonyms":"FAM54A,DUFD1","biotype":"protein_coding","ncbi_id":"113115","summary":null,"start":136231024,"end":136250335,"strand":-1,"description":"mitochondrial fission regulator 2 [Source:HGNC Symbol;Acc:HGNC:21115]"}, {"versioned_ensembl_gene_id":"ENSG00000253568.1","gene_symbol":"AC090572.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86776479,"end":86776638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214113.10","gene_symbol":"LYRM4","gene_name":"LYR motif containing 4 [Source:HGNC Symbol;Acc:HGNC:21365]","synonyms":"ISD11,CGI-203,C6orf149","biotype":"protein_coding","ncbi_id":"57128","summary":"The protein encoded by this gene is found in both mitochondria and the nucleus, where it binds cysteine desulfurase and helps free inorganic sulfur for Fe/S clusters. Disruption of this gene negatively impacts mitochondrial and cytosolic iron homeostasis. [provided by RefSeq, Sep 2016]","start":5102593,"end":5260939,"strand":-1,"description":"LYR motif containing 4 [Source:HGNC Symbol;Acc:HGNC:21365]"}, {"versioned_ensembl_gene_id":"ENSG00000204480.7","gene_symbol":"PRAMEF19","gene_name":"PRAME family member 19 [Source:HGNC Symbol;Acc:HGNC:24908]","synonyms":"OTTHUMG00000007919","biotype":"protein_coding","ncbi_id":"645414","summary":null,"start":13369067,"end":13371693,"strand":-1,"description":"PRAME family member 19 [Source:HGNC Symbol;Acc:HGNC:24908]"}, {"versioned_ensembl_gene_id":"ENSG00000225412.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32433363,"end":32446554,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000260335.1","gene_symbol":"AC133555.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29449191,"end":29449625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278638.1","gene_symbol":"AC244093.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37045462,"end":37052775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117222.13","gene_symbol":"RBBP5","gene_name":"RB binding protein 5, histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:9888]","synonyms":"SWD1,RBQ3","biotype":"protein_coding","ncbi_id":"5929","summary":"This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. The encoded protein binds directly to retinoblastoma protein, which regulates cell proliferation. It interacts preferentially with the underphosphorylated retinoblastoma protein via the E1A-binding pocket B. Three alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2010]","start":205086142,"end":205122015,"strand":-1,"description":"RB binding protein 5, histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:9888]"}, {"versioned_ensembl_gene_id":"ENSG00000004399.12","gene_symbol":"PLXND1","gene_name":"plexin D1 [Source:HGNC Symbol;Acc:HGNC:9107]","synonyms":"KIAA0620","biotype":"protein_coding","ncbi_id":"23129","summary":null,"start":129555175,"end":129606818,"strand":-1,"description":"plexin D1 [Source:HGNC Symbol;Acc:HGNC:9107]"}, {"versioned_ensembl_gene_id":"ENSG00000132824.13","gene_symbol":"SERINC3","gene_name":"serine incorporator 3 [Source:HGNC Symbol;Acc:HGNC:11699]","synonyms":"TMS-1,TDE1,TDE,SBBI99,DIFF33,AIGP1","biotype":"protein_coding","ncbi_id":"10955","summary":null,"start":44496221,"end":44522109,"strand":-1,"description":"serine incorporator 3 [Source:HGNC Symbol;Acc:HGNC:11699]"}, {"versioned_ensembl_gene_id":"ENSG00000259351.1","gene_symbol":"AC015914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63928274,"end":63935953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279307.2","gene_symbol":"AC012065.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20529467,"end":20529976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260302.1","gene_symbol":"AP005482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12774651,"end":12775923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183454.16","gene_symbol":"GRIN2A","gene_name":"glutamate ionotropic receptor NMDA type subunit 2A [Source:HGNC Symbol;Acc:HGNC:4585]","synonyms":"NMDAR2A,GluN2A","biotype":"protein_coding","ncbi_id":"2903","summary":"This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":9753404,"end":10182754,"strand":-1,"description":"glutamate ionotropic receptor NMDA type subunit 2A [Source:HGNC Symbol;Acc:HGNC:4585]"}, {"versioned_ensembl_gene_id":"ENSG00000275499.2","gene_symbol":"ZNF280A","gene_name":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]","synonyms":"ZNF636,ZNF280,SUHW1,3'OY11.1","biotype":"protein_coding","ncbi_id":"129025","summary":"This gene encodes a zinc finger protein. The encoded protein contains 4 C2H2-type zinc fingers, which are commonly found in transcription factors. A variety of functions may be performed by this type of zinc finger protein, including the binding of DNA or RNA. [provided by RefSeq, Apr 2014]","start":22522841,"end":22529375,"strand":-1,"description":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]"}, {"versioned_ensembl_gene_id":"ENSG00000143878.9","gene_symbol":"RHOB","gene_name":"ras homolog family member B [Source:HGNC Symbol;Acc:HGNC:668]","synonyms":"RHOH6,RhoB,MST081,ARHB,ARH6","biotype":"protein_coding","ncbi_id":"388","summary":null,"start":20447074,"end":20449445,"strand":1,"description":"ras homolog family member B [Source:HGNC Symbol;Acc:HGNC:668]"}, {"versioned_ensembl_gene_id":"ENSG00000203684.5","gene_symbol":"IBA57-AS1","gene_name":"IBA57 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:32062]","synonyms":"FLJ32878,C1orf148","biotype":"lincRNA","ncbi_id":"574432","summary":null,"start":228164086,"end":228165512,"strand":-1,"description":"IBA57 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:32062]"}, {"versioned_ensembl_gene_id":"ENSG00000237399.7","gene_symbol":"PITRM1-AS1","gene_name":"PITRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44675]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507034","summary":null,"start":3141632,"end":3167972,"strand":1,"description":"PITRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44675]"}, {"versioned_ensembl_gene_id":"ENSG00000163701.18","gene_symbol":"IL17RE","gene_name":"interleukin 17 receptor E [Source:HGNC Symbol;Acc:HGNC:18439]","synonyms":"FLJ23658","biotype":"protein_coding","ncbi_id":"132014","summary":"This gene encodes a transmembrane protein that functions as the receptor for interleukin-17C. The encoded protein signals to downstream components of the mitogen activated protein kinase (MAPK) pathway. Activity of this protein is important in the immune response to bacterial pathogens. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":9902612,"end":9916402,"strand":1,"description":"interleukin 17 receptor E [Source:HGNC Symbol;Acc:HGNC:18439]"}, {"versioned_ensembl_gene_id":"ENSG00000166862.6","gene_symbol":"CACNG2","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:1406]","synonyms":"stargazin,MGC138504,MGC138502","biotype":"protein_coding","ncbi_id":"10369","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. The AMPA subtype of ionotropic glutamate receptors are ligand gated ion channels that are typically activated by glutamate released from presynaptic neuron terminals and mediate fast neurotransmission in excitatory synapses. TARPs thus play an important role in synaptic plasticity, learning and memory. Mutations in this gene cause an autosomal dominant form of cognitive disability. [provided by RefSeq, Jul 2017]","start":36563921,"end":36703558,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:1406]"}, {"versioned_ensembl_gene_id":"ENSG00000070785.16","gene_symbol":"EIF2B3","gene_name":"eukaryotic translation initiation factor 2B subunit gamma [Source:HGNC Symbol;Acc:HGNC:3259]","synonyms":"EIF2Bgamma,EIF-2B","biotype":"protein_coding","ncbi_id":"8891","summary":"The protein encoded by this gene is one of the subunits of initiation factor eIF2B, which catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP. It has also been found to function as a cofactor of hepatitis C virus internal ribosome entry site-mediated translation. Mutations in this gene have been associated with leukodystrophy with vanishing white matter. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":44850522,"end":44986722,"strand":-1,"description":"eukaryotic translation initiation factor 2B subunit gamma [Source:HGNC Symbol;Acc:HGNC:3259]"}, {"versioned_ensembl_gene_id":"ENSG00000273976.1","gene_symbol":"GOLGA6L1","gene_name":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283767","summary":null,"start":23128268,"end":23136822,"strand":-1,"description":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]"}, {"versioned_ensembl_gene_id":"ENSG00000074590.13","gene_symbol":"NUAK1","gene_name":"NUAK family kinase 1 [Source:HGNC Symbol;Acc:HGNC:14311]","synonyms":"NuaK1,KIAA0537,ARK5","biotype":"protein_coding","ncbi_id":"9891","summary":null,"start":106063340,"end":106140033,"strand":-1,"description":"NUAK family kinase 1 [Source:HGNC Symbol;Acc:HGNC:14311]"}, {"versioned_ensembl_gene_id":"ENSG00000120156.20","gene_symbol":"TEK","gene_name":"TEK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11724]","synonyms":"TIE-2,CD202b,VMCM1,VMCM,TIE2","biotype":"protein_coding","ncbi_id":"7010","summary":"This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family. The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor and mediates a signaling pathway that functions in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]","start":27109141,"end":27230175,"strand":1,"description":"TEK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11724]"}, {"versioned_ensembl_gene_id":"ENSG00000253548.1","gene_symbol":"PYDC2","gene_name":"pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33512]","synonyms":"POP2","biotype":"protein_coding","ncbi_id":"152138","summary":null,"start":191461163,"end":191461456,"strand":1,"description":"pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33512]"}, {"versioned_ensembl_gene_id":"ENSG00000223812.6","gene_symbol":"AC073365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191425526,"end":191591097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107959.15","gene_symbol":"PITRM1","gene_name":"pitrilysin metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:17663]","synonyms":"PreP,MP1,KIAA1104,hMP1","biotype":"protein_coding","ncbi_id":"10531","summary":"The protein encoded by this gene is an ATP-dependent metalloprotease that degrades post-cleavage mitochondrial transit peptides. The encoded protein binds zinc and can also degrade amyloid beta A4 protein, suggesting a possible role in Alzheimer's disease. [provided by RefSeq, Dec 2016]","start":3137728,"end":3172841,"strand":-1,"description":"pitrilysin metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:17663]"}, {"versioned_ensembl_gene_id":"ENSG00000144445.16","gene_symbol":"KANSL1L","gene_name":"KAT8 regulatory NSL complex subunit 1 like [Source:HGNC Symbol;Acc:HGNC:26310]","synonyms":"MSL1v2,KIAA1267L,FLJ32349,FLJ23861,C2orf67","biotype":"protein_coding","ncbi_id":"151050","summary":null,"start":210021423,"end":210171383,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 1 like [Source:HGNC Symbol;Acc:HGNC:26310]"}, {"versioned_ensembl_gene_id":"ENSG00000173198.5","gene_symbol":"CYSLTR1","gene_name":"cysteinyl leukotriene receptor 1 [Source:HGNC Symbol;Acc:HGNC:17451]","synonyms":"CYSLT1R,CysLT1,CysLT(1)","biotype":"protein_coding","ncbi_id":"10800","summary":"This gene encodes a member of the G-protein coupled receptor 1 family. The encoded protein is a receptor for cysteinyl leukotrienes, and is involved in mediating bronchoconstriction via activation of a phosphatidylinositol-calcium second messenger system. Activation of the encoded receptor results in contraction and proliferation of bronchial smooth muscle cells, eosinophil migration, and damage to the mucus layer in the lung. Upregulation of this gene is associated with asthma and dysregulation may also be implicated in cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":78271464,"end":78327691,"strand":-1,"description":"cysteinyl leukotriene receptor 1 [Source:HGNC Symbol;Acc:HGNC:17451]"}, {"versioned_ensembl_gene_id":"ENSG00000126934.13","gene_symbol":"MAP2K2","gene_name":"mitogen-activated protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6842]","synonyms":"MEK2,PRKMK2","biotype":"protein_coding","ncbi_id":"5605","summary":"The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase is known to play a critical role in mitogen growth factor signal transduction. It phosphorylates and thus activates MAPK1/ERK2 and MAPK2/ERK3. The activation of this kinase itself is dependent on the Ser/Thr phosphorylation by MAP kinase kinase kinases. Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome), a disease characterized by heart defects, cognitive disability, and distinctive facial features similar to those found in Noonan syndrome. The inhibition or degradation of this kinase is also found to be involved in the pathogenesis of Yersinia and anthrax. A pseudogene, which is located on chromosome 7, has been identified for this gene. [provided by RefSeq, Jul 2008]","start":4090321,"end":4124129,"strand":-1,"description":"mitogen-activated protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6842]"}, {"versioned_ensembl_gene_id":"ENSG00000249240.2","gene_symbol":"AC069368.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":64841883,"end":64930920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255497.1","gene_symbol":"AC022616.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43313948,"end":43314200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228935.1","gene_symbol":"AL353132.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22960534,"end":22966063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198121.13","gene_symbol":"LPAR1","gene_name":"lysophosphatidic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:3166]","synonyms":"vzg-1,rec.1.3,Mrec1.3,LPA1,GPR26,Gpcr26,EDG2,edg-2","biotype":"protein_coding","ncbi_id":"1902","summary":"The integral membrane protein encoded by this gene is a lysophosphatidic acid (LPA) receptor from a group known as EDG receptors. These receptors are members of the G protein-coupled receptor superfamily. Utilized by LPA for cell signaling, EDG receptors mediate diverse biologic functions, including proliferation, platelet aggregation, smooth muscle contraction, inhibition of neuroblastoma cell differentiation, chemotaxis, and tumor cell invasion. Many transcript variants encoding a few different isoforms have been identified for this gene. [provided by RefSeq, Oct 2020]","start":110873263,"end":111038458,"strand":-1,"description":"lysophosphatidic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:3166]"}, {"versioned_ensembl_gene_id":"ENSG00000188877.12","gene_symbol":"POTEA","gene_name":"POTE ankyrin domain family member A [Source:HGNC Symbol;Acc:HGNC:33893]","synonyms":"POTE8,POTE-8,CT104.3,A26A1","biotype":"polymorphic_pseudogene","ncbi_id":"340441","summary":null,"start":43292483,"end":43363518,"strand":1,"description":"POTE ankyrin domain family member A [Source:HGNC Symbol;Acc:HGNC:33893]"}, {"versioned_ensembl_gene_id":"ENSG00000230492.1","gene_symbol":"AL049651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23010209,"end":23030785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232060.3","gene_symbol":"SLC4A1APP1","gene_name":"solute carrier family 4 member 1 adaptor protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288436","summary":null,"start":30558880,"end":30559481,"strand":-1,"description":"solute carrier family 4 member 1 adaptor protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49811]"}, {"versioned_ensembl_gene_id":"ENSG00000175556.16","gene_symbol":"LONRF3","gene_name":"LON peptidase N-terminal domain and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:21152]","synonyms":"RNF127,FLJ22612","biotype":"protein_coding","ncbi_id":"79836","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Multiple alternatively spliced transcript variants have been suggested, but their full length natures are not clear. [provided by RefSeq, Jul 2008]","start":118974614,"end":119018355,"strand":1,"description":"LON peptidase N-terminal domain and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:21152]"}, {"versioned_ensembl_gene_id":"ENSG00000282069.1","gene_symbol":"LINC02124","gene_name":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371048","summary":null,"start":1891136,"end":1892455,"strand":1,"description":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]"}, {"versioned_ensembl_gene_id":"ENSG00000261675.1","gene_symbol":"AL022313.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":36560870,"end":36562915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166839.16","gene_symbol":"ANKDD1A","gene_name":"ankyrin repeat and death domain containing 1A [Source:HGNC Symbol;Acc:HGNC:28002]","synonyms":"FLJ25870","biotype":"protein_coding","ncbi_id":"348094","summary":null,"start":64911902,"end":64958700,"strand":1,"description":"ankyrin repeat and death domain containing 1A [Source:HGNC Symbol;Acc:HGNC:28002]"}, {"versioned_ensembl_gene_id":"ENSG00000232800.1","gene_symbol":"SLC7A15P","gene_name":"solute carrier family 7 member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32724]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100289450","summary":null,"start":20386386,"end":20396588,"strand":1,"description":"solute carrier family 7 member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32724]"}, {"versioned_ensembl_gene_id":"ENSG00000232161.1","gene_symbol":"AC023141.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57770966,"end":57771173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186678.7","gene_symbol":"AL590240.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55172717,"end":55176026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055118.14","gene_symbol":"KCNH2","gene_name":"potassium voltage-gated channel subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:6251]","synonyms":"HERG,erg1,LQT2,Kv11.1","biotype":"protein_coding","ncbi_id":"3757","summary":"This gene encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":150944961,"end":150978315,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:6251]"}, {"versioned_ensembl_gene_id":"ENSG00000215018.9","gene_symbol":"COL28A1","gene_name":"collagen type XXVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340267","summary":"COL28A1 belongs to a class of collagens containing von Willebrand factor (VWF; MIM 613160) type A (VWFA) domains (Veit et al., 2006 [PubMed 16330543]).[supplied by OMIM, Nov 2010]","start":7356203,"end":7535853,"strand":-1,"description":"collagen type XXVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22442]"}, {"versioned_ensembl_gene_id":"ENSG00000070476.14","gene_symbol":"ZXDC","gene_name":"ZXD family zinc finger C [Source:HGNC Symbol;Acc:HGNC:28160]","synonyms":"MGC11349,FLJ13861","biotype":"protein_coding","ncbi_id":"79364","summary":null,"start":126437601,"end":126475919,"strand":-1,"description":"ZXD family zinc finger C [Source:HGNC Symbol;Acc:HGNC:28160]"}, {"versioned_ensembl_gene_id":"ENSG00000213111.5","gene_symbol":"COX5BP2","gene_name":"cytochrome c oxidase subunit 5B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2271]","synonyms":"COX5BL2","biotype":"transcribed_processed_pseudogene","ncbi_id":"1331","summary":null,"start":136034553,"end":136034886,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2271]"}, {"versioned_ensembl_gene_id":"ENSG00000277973.1","gene_symbol":"AL138828.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136206478,"end":136206860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274296.3","gene_symbol":"DECR2","gene_name":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]","synonyms":"SDR17C1,PDCR","biotype":"protein_coding","ncbi_id":"26063","summary":null,"start":401826,"end":412487,"strand":1,"description":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]"}, {"versioned_ensembl_gene_id":"ENSG00000237596.6","gene_symbol":"AL138828.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135991936,"end":136225751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011426.10","gene_symbol":"ANLN","gene_name":"anillin actin binding protein [Source:HGNC Symbol;Acc:HGNC:14082]","synonyms":"scra,ANILLIN,Scraps","biotype":"protein_coding","ncbi_id":"54443","summary":"This gene encodes an actin-binding protein that plays a role in cell growth and migration, and in cytokinesis. The encoded protein is thought to regulate actin cytoskeletal dynamics in podocytes, components of the glomerulus. Mutations in this gene are associated with focal segmental glomerulosclerosis 8. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":36389806,"end":36453791,"strand":1,"description":"anillin actin binding protein [Source:HGNC Symbol;Acc:HGNC:14082]"}, {"versioned_ensembl_gene_id":"ENSG00000225808.1","gene_symbol":"DNAJC19P5","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861453","summary":null,"start":177229191,"end":177229506,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45068]"}, {"versioned_ensembl_gene_id":"ENSG00000271825.1","gene_symbol":"AC019080.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177300600,"end":177302006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115705.20","gene_symbol":"TPO","gene_name":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]","synonyms":"TPX","biotype":"protein_coding","ncbi_id":"7173","summary":"This gene encodes a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones, thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis, including congenital hypothyroidism, congenital goiter, and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2011]","start":1374223,"end":1543711,"strand":1,"description":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]"}, {"versioned_ensembl_gene_id":"ENSG00000271996.1","gene_symbol":"AC019080.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177306373,"end":177310572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186188.10","gene_symbol":"FFAR4","gene_name":"free fatty acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:19061]","synonyms":"PGR4,O3FAR1,GPR129,GPR120","biotype":"protein_coding","ncbi_id":"338557","summary":"This gene encodes a G protein-coupled receptor (GPR) which belongs to the rhodopsin family of GPRs. The encoded protein functions as a receptor for free fatty acids, including omega-3, and participates in suppressing anti-inflammatory responses and insulin sensitizing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":93566665,"end":93604480,"strand":1,"description":"free fatty acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:19061]"}, {"versioned_ensembl_gene_id":"ENSG00000197860.9","gene_symbol":"SGTB","gene_name":"small glutamine rich tetratricopeptide repeat containing beta [Source:HGNC Symbol;Acc:HGNC:23567]","synonyms":"Sgt2,FLJ39002","biotype":"protein_coding","ncbi_id":"54557","summary":null,"start":65665928,"end":65723035,"strand":-1,"description":"small glutamine rich tetratricopeptide repeat containing beta [Source:HGNC Symbol;Acc:HGNC:23567]"}, {"versioned_ensembl_gene_id":"ENSG00000237178.2","gene_symbol":"AC019080.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177344443,"end":177344836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197321.14","gene_symbol":"SVIL","gene_name":"supervillin [Source:HGNC Symbol;Acc:HGNC:11480]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6840","summary":"This gene encodes a bipartite protein with distinct amino- and carboxy-terminal domains. The amino-terminus contains nuclear localization signals and the carboxy-terminus contains numerous consecutive sequences with extensive similarity to proteins in the gelsolin family of actin-binding proteins, which cap, nucleate, and/or sever actin filaments. The gene product is tightly associated with both actin filaments and plasma membranes, suggesting a role as a high-affinity link between the actin cytoskeleton and the membrane. The encoded protein appears to aid in both myosin II assembly during cell spreading and disassembly of focal adhesions. Several transcript variants encoding different isoforms of supervillin have been described. [provided by RefSeq, Apr 2016]","start":29457338,"end":29736781,"strand":-1,"description":"supervillin [Source:HGNC Symbol;Acc:HGNC:11480]"}, {"versioned_ensembl_gene_id":"ENSG00000184378.2","gene_symbol":"ACTRT3","gene_name":"actin related protein T3 [Source:HGNC Symbol;Acc:HGNC:24022]","synonyms":"ARPM1","biotype":"protein_coding","ncbi_id":"84517","summary":null,"start":169766921,"end":169769895,"strand":-1,"description":"actin related protein T3 [Source:HGNC Symbol;Acc:HGNC:24022]"}, {"versioned_ensembl_gene_id":"ENSG00000163359.15","gene_symbol":"COL6A3","gene_name":"collagen type VI alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2213]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1293","summary":"This gene encodes the alpha-3 chain, one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The alpha-3 chain of type VI collagen is much larger than the alpha-1 and -2 chains. This difference in size is largely due to an increase in the number of subdomains, similar to von Willebrand Factor type A domains, that are found in the amino terminal globular domain of all the alpha chains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in the type VI collagen genes are associated with Bethlem myopathy, a rare autosomal dominant proximal myopathy with early childhood onset. Mutations in this gene are also a cause of Ullrich congenital muscular dystrophy, also referred to as Ullrich scleroatonic muscular dystrophy, an autosomal recessive congenital myopathy that is more severe than Bethlem myopathy. Multiple transcript variants have been identified, but the full-length nature of only some of these variants has been described. [provided by RefSeq, Jun 2009]","start":237324003,"end":237414375,"strand":-1,"description":"collagen type VI alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2213]"}, {"versioned_ensembl_gene_id":"ENSG00000213963.6","gene_symbol":"AC019080.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":177283508,"end":177392691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234947.8","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31958721,"end":31968992,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000170509.11","gene_symbol":"HSD17B13","gene_name":"hydroxysteroid 17-beta dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:18685]","synonyms":"SDR16C3,SCDR9","biotype":"protein_coding","ncbi_id":"345275","summary":null,"start":87303789,"end":87322906,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:18685]"}, {"versioned_ensembl_gene_id":"ENSG00000153037.13","gene_symbol":"SRP19","gene_name":"signal recognition particle 19 [Source:HGNC Symbol;Acc:HGNC:11300]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6728","summary":null,"start":112861222,"end":112869788,"strand":1,"description":"signal recognition particle 19 [Source:HGNC Symbol;Acc:HGNC:11300]"}, {"versioned_ensembl_gene_id":"ENSG00000166037.10","gene_symbol":"CEP57","gene_name":"centrosomal protein 57 [Source:HGNC Symbol;Acc:HGNC:30794]","synonyms":"TSP57,Translokin,KIAA0092","biotype":"protein_coding","ncbi_id":"9702","summary":"This gene encodes a cytoplasmic protein called Translokin. This protein localizes to the centrosome and has a function in microtubular stabilization. The N-terminal half of this protein is required for its centrosome localization and for its multimerization, and the C-terminal half is required for nucleating, bundling and anchoring microtubules to the centrosomes. This protein specifically interacts with fibroblast growth factor 2 (FGF2), sorting nexin 6, Ran-binding protein M and the kinesins KIF3A and KIF3B, and thus mediates the nuclear translocation and mitogenic activity of the FGF2. It also interacts with cyclin D1 and controls nucleocytoplasmic distribution of the cyclin D1 in quiescent cells. This protein is crucial for maintaining correct chromosomal number during cell division. Mutations in this gene cause mosaic variegated aneuploidy syndrome, a rare autosomal recessive disorder. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":95789965,"end":95832693,"strand":1,"description":"centrosomal protein 57 [Source:HGNC Symbol;Acc:HGNC:30794]"}, {"versioned_ensembl_gene_id":"ENSG00000273955.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754987,"end":54767361,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000270397.1","gene_symbol":"AL670379.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120952344,"end":120952595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228517.2","gene_symbol":"CT47A7","gene_name":"cancer/testis antigen family 47, member A7 [Source:HGNC Symbol;Acc:HGNC:33288]","synonyms":"CT47.7","biotype":"protein_coding","ncbi_id":"653282","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120953288,"end":120956600,"strand":-1,"description":"cancer/testis antigen family 47, member A7 [Source:HGNC Symbol;Acc:HGNC:33288]"}, {"versioned_ensembl_gene_id":"ENSG00000235444.2","gene_symbol":"PSMB3P2","gene_name":"proteasome subunit beta 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130700","summary":null,"start":216610342,"end":216610959,"strand":-1,"description":"proteasome subunit beta 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30150]"}, {"versioned_ensembl_gene_id":"ENSG00000224391.1","gene_symbol":"LINC01280","gene_name":"long intergenic non-protein coding RNA 1280 [Source:HGNC Symbol;Acc:HGNC:50336]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928232","summary":null,"start":216590426,"end":216606938,"strand":-1,"description":"long intergenic non-protein coding RNA 1280 [Source:HGNC Symbol;Acc:HGNC:50336]"}, {"versioned_ensembl_gene_id":"ENSG00000280374.1","gene_symbol":"AC019080.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":177317715,"end":177318471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171408.13","gene_symbol":"PDE7B","gene_name":"phosphodiesterase 7B [Source:HGNC Symbol;Acc:HGNC:8792]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27115","summary":"The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a cAMP-specific phosphodiesterase, a member of the cyclic nucleotide phosphodiesterase family.[provided by RefSeq, Apr 2009]","start":135851696,"end":136195574,"strand":1,"description":"phosphodiesterase 7B [Source:HGNC Symbol;Acc:HGNC:8792]"}, {"versioned_ensembl_gene_id":"ENSG00000225794.1","gene_symbol":"AC073321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216604771,"end":216611202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228036.1","gene_symbol":"HSPD1P9","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35132]","synonyms":"HSPD1-14P","biotype":"processed_pseudogene","ncbi_id":"646910","summary":null,"start":37993085,"end":37994720,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35132]"}, {"versioned_ensembl_gene_id":"ENSG00000116044.15","gene_symbol":"NFE2L2","gene_name":"nuclear factor, erythroid 2 like 2 [Source:HGNC Symbol;Acc:HGNC:7782]","synonyms":"NRF2","biotype":"protein_coding","ncbi_id":"4780","summary":"This gene encodes a transcription factor which is a member of a small family of basic leucine zipper (bZIP) proteins. The encoded transcription factor regulates genes which contain antioxidant response elements (ARE) in their promoters; many of these genes encode proteins involved in response to injury and inflammation which includes the production of free radicals. Multiple transcript variants encoding different isoforms have been characterized for this gene. [provided by RefSeq, Sep 2015]","start":177227595,"end":177392697,"strand":-1,"description":"nuclear factor, erythroid 2 like 2 [Source:HGNC Symbol;Acc:HGNC:7782]"}, {"versioned_ensembl_gene_id":"ENSG00000237653.2","gene_symbol":"AC026320.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":191952349,"end":191952826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274317.1","gene_symbol":"LINC02334","gene_name":"long intergenic non-protein coding RNA 2334 [Source:HGNC Symbol;Acc:HGNC:53254]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929077","summary":null,"start":37934565,"end":38048169,"strand":1,"description":"long intergenic non-protein coding RNA 2334 [Source:HGNC Symbol;Acc:HGNC:53254]"}, {"versioned_ensembl_gene_id":"ENSG00000232353.5","gene_symbol":"AC026320.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":192029880,"end":192036557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219807.2","gene_symbol":"ARF1P1","gene_name":"ADP ribosylation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442334","summary":null,"start":94833904,"end":94834447,"strand":1,"description":"ADP ribosylation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22500]"}, {"versioned_ensembl_gene_id":"ENSG00000228521.2","gene_symbol":"AC099552.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155204147,"end":155205189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271502.1","gene_symbol":"AL670379.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120957227,"end":120957479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226023.6","gene_symbol":"CT47A6","gene_name":"cancer/testis antigen family 47, member A6 [Source:HGNC Symbol;Acc:HGNC:33287]","synonyms":"CT47.6","biotype":"protein_coding","ncbi_id":"728062","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120958165,"end":120961487,"strand":-1,"description":"cancer/testis antigen family 47, member A6 [Source:HGNC Symbol;Acc:HGNC:33287]"}, {"versioned_ensembl_gene_id":"ENSG00000239792.2","gene_symbol":"C2orf27AP2","gene_name":"chromosome 2 open reading frame 27A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49813]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100131855","summary":null,"start":30670964,"end":30671966,"strand":-1,"description":"chromosome 2 open reading frame 27A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49813]"}, {"versioned_ensembl_gene_id":"ENSG00000225612.1","gene_symbol":"AC099552.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155267299,"end":155268052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115457.9","gene_symbol":"IGFBP2","gene_name":"insulin like growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5471]","synonyms":"IBP2","biotype":"protein_coding","ncbi_id":"3485","summary":"The protein encoded by this gene is one of six similar proteins that bind insulin-like growth factors I and II (IGF-I and IGF-II). The encoded protein can be secreted into the bloodstream, where it binds IGF-I and IGF-II with high affinity, or it can remain intracellular, interacting with many different ligands. High expression levels of this protein promote the growth of several types of tumors and may be predictive of the chances of recovery of the patient. Several transcript variants, one encoding a secreted isoform and the others encoding nonsecreted isoforms, have been found for this gene. [provided by RefSeq, Sep 2015]","start":216632828,"end":216664436,"strand":1,"description":"insulin like growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5471]"}, {"versioned_ensembl_gene_id":"ENSG00000273481.1","gene_symbol":"AL391069.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151327949,"end":151328429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215210.3","gene_symbol":"RBMXP2","gene_name":"RNA binding motif protein, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23284]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441391","summary":null,"start":30689105,"end":30690272,"strand":1,"description":"RNA binding motif protein, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23284]"}, {"versioned_ensembl_gene_id":"ENSG00000273117.1","gene_symbol":"AC144652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155295918,"end":155297541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184945.13","gene_symbol":"AQP12A","gene_name":"aquaporin 12A [Source:HGNC Symbol;Acc:HGNC:19941]","synonyms":"AQP12","biotype":"protein_coding","ncbi_id":"375318","summary":null,"start":240691845,"end":240698483,"strand":1,"description":"aquaporin 12A [Source:HGNC Symbol;Acc:HGNC:19941]"}, {"versioned_ensembl_gene_id":"ENSG00000111052.7","gene_symbol":"LIN7A","gene_name":"lin-7 homolog A, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17787]","synonyms":"VELI1,TIP-33,MALS-1,LIN-7A","biotype":"protein_coding","ncbi_id":"8825","summary":"The protein encoded by this gene is involved in generating and maintaining the asymmetric distribution of channels and receptors at the cell membrane. The encoded protein also is required for the localization of some specific channels and can be part of a protein complex that couples synaptic vesicle exocytosis to cell adhesion in the brain. [provided by RefSeq, May 2016]","start":80792520,"end":80937925,"strand":-1,"description":"lin-7 homolog A, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17787]"}, {"versioned_ensembl_gene_id":"ENSG00000238216.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"NCRNA00149,AB023051.1","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30780908,"end":30784476,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000276385.1","gene_symbol":"AL445567.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8934984,"end":8935481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259920.1","gene_symbol":"AC007938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130481491,"end":130484392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130513.6","gene_symbol":"GDF15","gene_name":"growth differentiation factor 15 [Source:HGNC Symbol;Acc:HGNC:30142]","synonyms":"PLAB,PDF,NAG-1,MIC1,MIC-1,PTGFB","biotype":"protein_coding","ncbi_id":"9518","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The protein is expressed in a broad range of cell types, acts as a pleiotropic cytokine and is involved in the stress response program of cells after cellular injury. Increased protein levels are associated with disease states such as tissue hypoxia, inflammation, acute injury and oxidative stress. [provided by RefSeq, Aug 2016]","start":18374731,"end":18389176,"strand":1,"description":"growth differentiation factor 15 [Source:HGNC Symbol;Acc:HGNC:30142]"}, {"versioned_ensembl_gene_id":"ENSG00000239314.1","gene_symbol":"MORC1-AS1","gene_name":"MORC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40377]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506506","summary":null,"start":109101456,"end":109110342,"strand":1,"description":"MORC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40377]"}, {"versioned_ensembl_gene_id":"ENSG00000114487.9","gene_symbol":"MORC1","gene_name":"MORC family CW-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:7198]","synonyms":"ZCW6,MORC,CT33","biotype":"protein_coding","ncbi_id":"27136","summary":"This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009]","start":108958239,"end":109118142,"strand":-1,"description":"MORC family CW-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:7198]"}, {"versioned_ensembl_gene_id":"ENSG00000224808.1","gene_symbol":"SRGAP3-AS1","gene_name":"SRGAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40898]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874103","summary":null,"start":9014123,"end":9015979,"strand":1,"description":"SRGAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40898]"}, {"versioned_ensembl_gene_id":"ENSG00000105401.8","gene_symbol":"CDC37","gene_name":"cell division cycle 37 [Source:HGNC Symbol;Acc:HGNC:1735]","synonyms":"P50CDC37","biotype":"protein_coding","ncbi_id":"11140","summary":"The protein encoded by this gene is highly similar to Cdc 37, a cell division cycle control protein of Sacchromyces cerevisiae. This protein is a molecular chaperone with specific function in cell signal transduction. It has been shown to form complex with Hsp90 and a variety of protein kinases including CDK4, CDK6, SRC, RAF-1, MOK, as well as eIF2 alpha kinases. It is thought to play a critical role in directing Hsp90 to its target kinases. [provided by RefSeq, Jul 2008]","start":10391134,"end":10420121,"strand":-1,"description":"cell division cycle 37 [Source:HGNC Symbol;Acc:HGNC:1735]"}, {"versioned_ensembl_gene_id":"ENSG00000235830.1","gene_symbol":"SRGAP3-AS4","gene_name":"SRGAP3 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42434]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927440","summary":null,"start":9256759,"end":9257507,"strand":1,"description":"SRGAP3 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:42434]"}, {"versioned_ensembl_gene_id":"ENSG00000225773.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31927103,"end":31934377,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000108442.2","gene_symbol":"TVP23BP2","gene_name":"TVP23B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38869]","synonyms":"FAM18B4P","biotype":"processed_pseudogene","ncbi_id":"100421473","summary":null,"start":74628328,"end":74628942,"strand":-1,"description":"TVP23B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38869]"}, {"versioned_ensembl_gene_id":"ENSG00000233877.2","gene_symbol":"AL606517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64941979,"end":64942365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159374.17","gene_symbol":"M1AP","gene_name":"meiosis 1 associated protein [Source:HGNC Symbol;Acc:HGNC:25183]","synonyms":"SPATA37,D6Mm5e,C2orf65","biotype":"protein_coding","ncbi_id":"130951","summary":"This gene encodes a protein that is likely to function in progression of meiosis. A similar protein in mouse plays a role in gametogenesis in both sexes. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":74557883,"end":74648338,"strand":-1,"description":"meiosis 1 associated protein [Source:HGNC Symbol;Acc:HGNC:25183]"}, {"versioned_ensembl_gene_id":"ENSG00000270426.1","gene_symbol":"AC099343.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":184471924,"end":184472609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240389.5","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"NG3,C6orf8","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32231591,"end":32235290,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000277535.2","gene_symbol":"AL772284.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":119073226,"end":119076373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183747.11","gene_symbol":"ACSM2A","gene_name":"acyl-CoA synthetase medium chain family member 2A [Source:HGNC Symbol;Acc:HGNC:32017]","synonyms":"MGC150530,ACSM2,A-923A4.1","biotype":"protein_coding","ncbi_id":"123876","summary":"This gene encodes a mitochondrial acyl-coenzyme A synthetase that is specific for medium chain fatty acids. These enzymes catalyze fatty acid activation, the first step of fatty acid metabolism, through the transfer of acyl-CoA. These enzymes also participate in the glycine conjugation pathway in the detoxification of xenobiotics such as benzoate and ibuprofen. Expression levels of this gene in the kidney may be correlated with kidney function. This gene and its paralog ACSM2B (Gene ID: 348158), both present on chromosome 16, likely arose from a chromosomal duplication event. [provided by RefSeq, May 2017]","start":20451461,"end":20487667,"strand":1,"description":"acyl-CoA synthetase medium chain family member 2A [Source:HGNC Symbol;Acc:HGNC:32017]"}, {"versioned_ensembl_gene_id":"ENSG00000237459.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"NG31,C6orf25,G6b-B,G6b","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31794876,"end":31802992,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000168310.10","gene_symbol":"IRF2","gene_name":"interferon regulatory factor 2 [Source:HGNC Symbol;Acc:HGNC:6117]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3660","summary":"IRF2 encodes interferon regulatory factor 2, a member of the interferon regulatory transcription factor (IRF) family. IRF2 competitively inhibits the IRF1-mediated transcriptional activation of interferons alpha and beta, and presumably other genes that employ IRF1 for transcription activation. However, IRF2 also functions as a transcriptional activator of histone H4. [provided by RefSeq, Jul 2008]","start":184387713,"end":184474580,"strand":-1,"description":"interferon regulatory factor 2 [Source:HGNC Symbol;Acc:HGNC:6117]"}, {"versioned_ensembl_gene_id":"ENSG00000235626.2","gene_symbol":"KRT18P66","gene_name":"keratin 18 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442405","summary":null,"start":30773464,"end":30774732,"strand":1,"description":"keratin 18 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48893]"}, {"versioned_ensembl_gene_id":"ENSG00000226246.1","gene_symbol":"KRT18P36","gene_name":"keratin 18 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:33405]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442406","summary":null,"start":30799471,"end":30800746,"strand":-1,"description":"keratin 18 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:33405]"}, {"versioned_ensembl_gene_id":"ENSG00000234784.2","gene_symbol":"AL606517.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64918443,"end":64918683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184624.4","gene_symbol":"ZNF72P","gene_name":"zinc finger protein 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:13142]","synonyms":"ZNF72,Cos8","biotype":"unprocessed_pseudogene","ncbi_id":"100287084","summary":null,"start":15326037,"end":15343065,"strand":-1,"description":"zinc finger protein 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:13142]"}, {"versioned_ensembl_gene_id":"ENSG00000171060.10","gene_symbol":"C8orf74","gene_name":"chromosome 8 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:32296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203076","summary":null,"start":10672637,"end":10700593,"strand":1,"description":"chromosome 8 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:32296]"}, {"versioned_ensembl_gene_id":"ENSG00000276411.1","gene_symbol":"AC106875.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11673964,"end":11676925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236097.1","gene_symbol":"BNIP3P2","gene_name":"BCL2 interacting protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39655]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421754","summary":null,"start":15349467,"end":15350043,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39655]"}, {"versioned_ensembl_gene_id":"ENSG00000242539.2","gene_symbol":"AC007620.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179396961,"end":179399191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236831.1","gene_symbol":"YME1L1P1","gene_name":"YME1L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12844]","synonyms":"YME1L2","biotype":"unprocessed_pseudogene","ncbi_id":"23749","summary":null,"start":15489990,"end":15492564,"strand":1,"description":"YME1L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12844]"}, {"versioned_ensembl_gene_id":"ENSG00000272699.1","gene_symbol":"AC007620.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179405448,"end":179405944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114450.9","gene_symbol":"GNB4","gene_name":"G protein subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:20731]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59345","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. [provided by RefSeq, Jul 2008]","start":179396089,"end":179451590,"strand":-1,"description":"G protein subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:20731]"}, {"versioned_ensembl_gene_id":"ENSG00000162434.11","gene_symbol":"JAK1","gene_name":"Janus kinase 1 [Source:HGNC Symbol;Acc:HGNC:6190]","synonyms":"JTK3,JAK1B,JAK1A","biotype":"protein_coding","ncbi_id":"3716","summary":"This gene encodes a membrane protein that is a member of a class of protein-tyrosine kinases (PTK) characterized by the presence of a second phosphotransferase-related domain immediately N-terminal to the PTK domain. The encoded kinase phosphorylates STAT proteins (signal transducers and activators of transcription) and plays a key role in interferon-alpha/beta, interferon-gamma, and cytokine signal transduction. This gene plays a crucial role in effecting the expression of genes that mediate inflammation, epithelial remodeling, and metastatic cancer progression. This gene is a key component of the interleukin-6 (IL-6)/JAK1/STAT3 immune and inflammation response and is a therapeutic target for alleviating cytokine storms. The kinase activity of this gene is directly inhibited by the suppressor of cytokine signalling 1 (SOCS1) protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":64833229,"end":64966504,"strand":-1,"description":"Janus kinase 1 [Source:HGNC Symbol;Acc:HGNC:6190]"}, {"versioned_ensembl_gene_id":"ENSG00000274092.1","gene_symbol":"AC106739.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27313387,"end":27314101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107554.16","gene_symbol":"DNMBP","gene_name":"dynamin binding protein [Source:HGNC Symbol;Acc:HGNC:30373]","synonyms":"KIAA1010,ARHGEF36,Tuba","biotype":"protein_coding","ncbi_id":"23268","summary":"This gene encodes a protein belonging to the guanine nucleotide exchange factor family, and which regulates the configuration of cell junctions. It contains multiple binding sites for dynamin and thus links dynamin to actin regulatory proteins. Polymorphisms in this gene have been linked to Alzheimer's disease in some populations, though there are conflicting reports of such linkages in other populations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":99875577,"end":100009919,"strand":-1,"description":"dynamin binding protein [Source:HGNC Symbol;Acc:HGNC:30373]"}, {"versioned_ensembl_gene_id":"ENSG00000130538.4","gene_symbol":"OR11H1","gene_name":"olfactory receptor family 11 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15404]","synonyms":"OR22-1","biotype":"protein_coding","ncbi_id":"81061","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15528158,"end":15529139,"strand":1,"description":"olfactory receptor family 11 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15404]"}, {"versioned_ensembl_gene_id":"ENSG00000272389.1","gene_symbol":"AC008536.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112898023,"end":112898371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256151.1","gene_symbol":"ADGRD1-AS1","gene_name":"ADGRD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53314]","synonyms":"LACAT8","biotype":"lincRNA","ncbi_id":"105755954","summary":null,"start":130990138,"end":130993976,"strand":-1,"description":"ADGRD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53314]"}, {"versioned_ensembl_gene_id":"ENSG00000149452.15","gene_symbol":"SLC22A8","gene_name":"solute carrier family 22 member 8 [Source:HGNC Symbol;Acc:HGNC:10972]","synonyms":"OAT3","biotype":"protein_coding","ncbi_id":"9376","summary":"This gene encodes a protein involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, May 2010]","start":62989154,"end":63015839,"strand":-1,"description":"solute carrier family 22 member 8 [Source:HGNC Symbol;Acc:HGNC:10972]"}, {"versioned_ensembl_gene_id":"ENSG00000258864.1","gene_symbol":"AC008575.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112827213,"end":112867582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168917.8","gene_symbol":"SLC35G2","gene_name":"solute carrier family 35 member G2 [Source:HGNC Symbol;Acc:HGNC:28480]","synonyms":"MGC3295,DKFZp564K2464,TMEM22","biotype":"protein_coding","ncbi_id":"80723","summary":null,"start":136818647,"end":136855892,"strand":1,"description":"solute carrier family 35 member G2 [Source:HGNC Symbol;Acc:HGNC:28480]"}, {"versioned_ensembl_gene_id":"ENSG00000237299.1","gene_symbol":"AP000534.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15541436,"end":15578006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134982.16","gene_symbol":"APC","gene_name":"APC, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:583]","synonyms":"PPP1R46,DP3,DP2.5,DP2","biotype":"protein_coding","ncbi_id":"324","summary":"This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Mutations in the APC gene have been found to occur in most colorectal cancers. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Dec 2019]","start":112707498,"end":112846239,"strand":1,"description":"APC, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:583]"}, {"versioned_ensembl_gene_id":"ENSG00000257658.1","gene_symbol":"AC004217.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112321759,"end":112323089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111058.7","gene_symbol":"ACSS3","gene_name":"acyl-CoA synthetase short chain family member 3 [Source:HGNC Symbol;Acc:HGNC:24723]","synonyms":"FLJ21963","biotype":"protein_coding","ncbi_id":"79611","summary":null,"start":80936414,"end":81261205,"strand":1,"description":"acyl-CoA synthetase short chain family member 3 [Source:HGNC Symbol;Acc:HGNC:24723]"}, {"versioned_ensembl_gene_id":"ENSG00000213727.3","gene_symbol":"AP000533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15572089,"end":15573265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235759.1","gene_symbol":"ARHGAP42P3","gene_name":"Rho GTPase activating protein 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19327]","synonyms":"OPHN1P1","biotype":"processed_pseudogene","ncbi_id":"266698","summary":null,"start":15550904,"end":15553838,"strand":-1,"description":"Rho GTPase activating protein 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19327]"}, {"versioned_ensembl_gene_id":"ENSG00000239213.5","gene_symbol":"NCK1-AS1","gene_name":"NCK1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49645]","synonyms":"SLC35G2-AS1","biotype":"antisense_RNA","ncbi_id":"101927597","summary":null,"start":136841726,"end":136862054,"strand":-1,"description":"NCK1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49645]"}, {"versioned_ensembl_gene_id":"ENSG00000173064.12","gene_symbol":"HECTD4","gene_name":"HECT domain E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:26611]","synonyms":"FLJ34154,C12orf51,KIAA0614","biotype":"protein_coding","ncbi_id":"283450","summary":null,"start":112160188,"end":112382439,"strand":-1,"description":"HECT domain E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:26611]"}, {"versioned_ensembl_gene_id":"ENSG00000233408.1","gene_symbol":"AP000534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15557577,"end":15560694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183638.5","gene_symbol":"RP1L1","gene_name":"RP1 like 1 [Source:HGNC Symbol;Acc:HGNC:15946]","synonyms":"DCDC4B","biotype":"protein_coding","ncbi_id":"94137","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, and two C-terminal large repetitive regions, both of which contain a high percentage of glutamine and glutamic acid residues. This protein is a retinal-specific protein. Its exact length varies among individuals due to the presence of a 16aa repeat in the first C-terminal repetitive region. The 16aa repeat is encoded by the highly polymorphic 48-bp repeat, and 1-6 copies of the 16aa repeat have been identified in normal individuals. The current reference sequence shown here has a single copy of the 16aa repeat. This protein and the RP1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Mutations in this gene cause occult macular dystrophy (OMD). [provided by RefSeq, Sep 2010]","start":10606349,"end":10712187,"strand":-1,"description":"RP1 like 1 [Source:HGNC Symbol;Acc:HGNC:15946]"}, {"versioned_ensembl_gene_id":"ENSG00000215268.3","gene_symbol":"AP000533.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15562017,"end":15564276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174529.7","gene_symbol":"TMEM81","gene_name":"transmembrane protein 81 [Source:HGNC Symbol;Acc:HGNC:32349]","synonyms":"UNQ2788,MGC75217,KVLA2788,HC3107","biotype":"protein_coding","ncbi_id":"388730","summary":null,"start":205083129,"end":205084460,"strand":-1,"description":"transmembrane protein 81 [Source:HGNC Symbol;Acc:HGNC:32349]"}, {"versioned_ensembl_gene_id":"ENSG00000254344.1","gene_symbol":"LINC01288","gene_name":"long intergenic non-protein coding RNA 1288 [Source:HGNC Symbol;Acc:HGNC:50353]","synonyms":"TCONS_00014671","biotype":"lincRNA","ncbi_id":"103689844","summary":null,"start":34784052,"end":34864798,"strand":1,"description":"long intergenic non-protein coding RNA 1288 [Source:HGNC Symbol;Acc:HGNC:50353]"}, {"versioned_ensembl_gene_id":"ENSG00000230274.1","gene_symbol":"PGAM1P3","gene_name":"phosphoglycerate mutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873887","summary":null,"start":40322715,"end":40323279,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42450]"}, {"versioned_ensembl_gene_id":"ENSG00000282145.1","gene_symbol":"AC243913.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28687420,"end":28691285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223797.5","gene_symbol":"ENTPD3-AS1","gene_name":"ENTPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26710]","synonyms":"FLJ36665","biotype":"antisense_RNA","ncbi_id":"285266","summary":null,"start":40313802,"end":40453329,"strand":-1,"description":"ENTPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26710]"}, {"versioned_ensembl_gene_id":"ENSG00000274870.1","gene_symbol":"OR2T4","gene_name":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]","synonyms":"OR2T4Q","biotype":"protein_coding","ncbi_id":"127074","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248361581,"end":248362627,"strand":1,"description":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]"}, {"versioned_ensembl_gene_id":"ENSG00000243181.2","gene_symbol":"AC087343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34874159,"end":34874633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235479.1","gene_symbol":"RAB9AP4","gene_name":"RAB9A, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38108]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288397","summary":null,"start":18649671,"end":18650279,"strand":1,"description":"RAB9A, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38108]"}, {"versioned_ensembl_gene_id":"ENSG00000284684.1","gene_symbol":"AC092442.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6064977,"end":6070162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225682.6","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31957356,"end":31959838,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000273486.1","gene_symbol":"AC096992.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136837338,"end":136839021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282444.1","gene_symbol":"AC243913.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28695142,"end":28702879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275785.1","gene_symbol":"AC015914.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63890030,"end":63890317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225569.1","gene_symbol":"CCT4P2","gene_name":"chaperonin containing TCP1 subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131638","summary":null,"start":65270913,"end":65273019,"strand":1,"description":"chaperonin containing TCP1 subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35141]"}, {"versioned_ensembl_gene_id":"ENSG00000249115.8","gene_symbol":"HAUS5","gene_name":"HAUS augmin like complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29130]","synonyms":"KIAA0841,dgt5","biotype":"protein_coding","ncbi_id":"23354","summary":"HAUS5 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]","start":35612744,"end":35625349,"strand":1,"description":"HAUS augmin like complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29130]"}, {"versioned_ensembl_gene_id":"ENSG00000111452.12","gene_symbol":"ADGRD1","gene_name":"adhesion G protein-coupled receptor D1 [Source:HGNC Symbol;Acc:HGNC:19893]","synonyms":"PGR25,GPR133,DKFZp434B1272","biotype":"protein_coding","ncbi_id":"283383","summary":"The adhesion G-protein-coupled receptors (GPCRs), including GPR133, are membrane-bound proteins with long N termini containing multiple domains. GPCRs, or GPRs, contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins (summary by Bjarnadottir et al., 2004 [PubMed 15203201]).[supplied by OMIM, Nov 2010]","start":130953907,"end":131141469,"strand":1,"description":"adhesion G protein-coupled receptor D1 [Source:HGNC Symbol;Acc:HGNC:19893]"}, {"versioned_ensembl_gene_id":"ENSG00000254342.1","gene_symbol":"AC022616.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43372559,"end":43372677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233872.1","gene_symbol":"AC005033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74618856,"end":74620979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251322.7","gene_symbol":"SHANK3","gene_name":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]","synonyms":"SPANK-2,PSAP2,prosap2,KIAA1650","biotype":"protein_coding","ncbi_id":"85358","summary":"This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]","start":50674415,"end":50733298,"strand":1,"description":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]"}, {"versioned_ensembl_gene_id":"ENSG00000250637.2","gene_symbol":"AC134698.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43442902,"end":43452912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168907.13","gene_symbol":"PLA2G4F","gene_name":"phospholipase A2 group IVF [Source:HGNC Symbol;Acc:HGNC:27396]","synonyms":"PLA2G4F/Z","biotype":"protein_coding","ncbi_id":"255189","summary":null,"start":42139034,"end":42156636,"strand":-1,"description":"phospholipase A2 group IVF [Source:HGNC Symbol;Acc:HGNC:27396]"}, {"versioned_ensembl_gene_id":"ENSG00000223685.5","gene_symbol":"LINC00571","gene_name":"long intergenic non-protein coding RNA 571 [Source:HGNC Symbol;Acc:HGNC:43721]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874188","summary":null,"start":38050817,"end":38143232,"strand":-1,"description":"long intergenic non-protein coding RNA 571 [Source:HGNC Symbol;Acc:HGNC:43721]"}, {"versioned_ensembl_gene_id":"ENSG00000248573.1","gene_symbol":"PRYP6","gene_name":"PTPN13-like, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38786]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106480721","summary":null,"start":18790709,"end":18791051,"strand":-1,"description":"PTPN13-like, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38786]"}, {"versioned_ensembl_gene_id":"ENSG00000242153.7","gene_symbol":"OFD1P6Y","gene_name":"OFD1 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:13657]","synonyms":"OFDYP6,OFD1PY6,OFD1P6,OFD1P2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"386690","summary":null,"start":18674033,"end":18739197,"strand":1,"description":"OFD1 pseudogene 6, Y-linked [Source:HGNC Symbol;Acc:HGNC:13657]"}, {"versioned_ensembl_gene_id":"ENSG00000252554.1","gene_symbol":"RNU6-861P","gene_name":"RNA, U6 small nuclear 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:47824]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479947","summary":null,"start":129436875,"end":129436980,"strand":-1,"description":"RNA, U6 small nuclear 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:47824]"}, {"versioned_ensembl_gene_id":"ENSG00000273727.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":120354987,"end":120355148,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000222942.1","gene_symbol":"RN7SKP58","gene_name":"RNA, 7SK small nuclear pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:45782]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480850","summary":null,"start":41766615,"end":41766919,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:45782]"}, {"versioned_ensembl_gene_id":"ENSG00000199985.1","gene_symbol":"RNA5SP264","gene_name":"RNA, 5S ribosomal pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:43164]","synonyms":"RN5S264","biotype":"rRNA","ncbi_id":"100873517","summary":null,"start":36764445,"end":36764551,"strand":1,"description":"RNA, 5S ribosomal pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:43164]"}, {"versioned_ensembl_gene_id":"ENSG00000200890.1","gene_symbol":"RNA5SP99","gene_name":"RNA, 5S ribosomal pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:42897]","synonyms":"RN5S99","biotype":"rRNA","ncbi_id":"106478993","summary":null,"start":81496214,"end":81496327,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:42897]"}, {"versioned_ensembl_gene_id":"ENSG00000206710.1","gene_symbol":"RNU6-147P","gene_name":"RNA, U6 small nuclear 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:47110]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480556","summary":null,"start":49972106,"end":49972212,"strand":1,"description":"RNA, U6 small nuclear 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:47110]"}, {"versioned_ensembl_gene_id":"ENSG00000252947.1","gene_symbol":"SCARNA1","gene_name":"small Cajal body-specific RNA 1 [Source:HGNC Symbol;Acc:HGNC:32555]","synonyms":"ACA35","biotype":"scaRNA","ncbi_id":"677774","summary":null,"start":27834401,"end":27834566,"strand":1,"description":"small Cajal body-specific RNA 1 [Source:HGNC Symbol;Acc:HGNC:32555]"}, {"versioned_ensembl_gene_id":"ENSG00000241785.3","gene_symbol":"RN7SL390P","gene_name":"RNA, 7SL, cytoplasmic 390, pseudogene [Source:HGNC Symbol;Acc:HGNC:46406]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479366","summary":null,"start":54255627,"end":54255910,"strand":-1,"description":"RNA, 7SL, cytoplasmic 390, pseudogene [Source:HGNC Symbol;Acc:HGNC:46406]"}, {"versioned_ensembl_gene_id":"ENSG00000222920.1","gene_symbol":"RNA5SP29","gene_name":"RNA, 5S ribosomal pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42605]","synonyms":"RN5S29","biotype":"rRNA","ncbi_id":"100873361","summary":null,"start":51027747,"end":51027852,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42605]"}, {"versioned_ensembl_gene_id":"ENSG00000264910.2","gene_symbol":"RN7SL525P","gene_name":"RNA, 7SL, cytoplasmic 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:46541]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480516","summary":null,"start":58543299,"end":58543578,"strand":-1,"description":"RNA, 7SL, cytoplasmic 525, pseudogene [Source:HGNC Symbol;Acc:HGNC:46541]"}, {"versioned_ensembl_gene_id":"ENSG00000206921.1","gene_symbol":"RNU6-481P","gene_name":"RNA, U6 small nuclear 481, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000277965.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38711821,"end":38712103,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276601.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58785323,"end":58785608,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266747.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31445150,"end":31445248,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251936.1","gene_symbol":"RNA5SP249","gene_name":"RNA, 5S ribosomal pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:43149]","synonyms":"RN5S249","biotype":"rRNA","ncbi_id":"100873505","summary":null,"start":147849884,"end":147849982,"strand":1,"description":"RNA, 5S ribosomal pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:43149]"}, {"versioned_ensembl_gene_id":"ENSG00000206772.1","gene_symbol":"RNU6-44P","gene_name":"RNA, U6 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:34288]","synonyms":"RNU6-44","biotype":"snRNA","ncbi_id":"106478922","summary":null,"start":112352556,"end":112352662,"strand":-1,"description":"RNA, U6 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:34288]"}, {"versioned_ensembl_gene_id":"ENSG00000252297.1","gene_symbol":"RNU6-875P","gene_name":"RNA, U6 small nuclear 875, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000242559.3","gene_symbol":"RN7SL144P","gene_name":"RNA, 7SL, cytoplasmic 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:46160]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480960","summary":null,"start":41683168,"end":41683462,"strand":-1,"description":"RNA, 7SL, cytoplasmic 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:46160]"}, {"versioned_ensembl_gene_id":"ENSG00000265795.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28915634,"end":28915733,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200274.1","gene_symbol":"RNU4-32P","gene_name":"RNA, U4 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46968]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479572","summary":null,"start":109567975,"end":109568115,"strand":-1,"description":"RNA, U4 small nuclear 32, 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Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]","start":25041974,"end":25042040,"strand":1,"description":"small nucleolar RNA, C/D box 109A [Source:HGNC Symbol;Acc:HGNC:32773]"}, {"versioned_ensembl_gene_id":"ENSG00000252950.1","gene_symbol":"RNA5SP490","gene_name":"RNA, 5S ribosomal pseudogene 490 [Source:HGNC Symbol;Acc:HGNC:43390]","synonyms":"RN5S490","biotype":"rRNA","ncbi_id":"100873732","summary":null,"start":32563075,"end":32563210,"strand":1,"description":"RNA, 5S ribosomal pseudogene 490 [Source:HGNC Symbol;Acc:HGNC:43390]"}, {"versioned_ensembl_gene_id":"ENSG00000201048.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10674658,"end":10674768,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207013.1","gene_symbol":"RNU6-804P","gene_name":"RNA, U6 small nuclear 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:47767]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479921","summary":null,"start":86663144,"end":86663250,"strand":-1,"description":"RNA, U6 small nuclear 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:47767]"}, {"versioned_ensembl_gene_id":"ENSG00000252294.1","gene_symbol":"RNU6-589P","gene_name":"RNA, U6 small nuclear 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:47552]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481367","summary":null,"start":102678707,"end":102678813,"strand":-1,"description":"RNA, U6 small nuclear 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:47552]"}, {"versioned_ensembl_gene_id":"ENSG00000281766.2","gene_symbol":"RYBP","gene_name":"RING1 and YY1 binding protein [Source:NCBI gene;Acc:23429]","synonyms":"DEDAF,YEAF1,AAP1,DEDAF,APAP-1,AAP1,YEAF1","biotype":"protein_coding","ncbi_id":"23429","summary":null,"start":72378406,"end":72447301,"strand":-1,"description":"RING1 and YY1 binding protein [Source:NCBI gene;Acc:23429]"}, {"versioned_ensembl_gene_id":"ENSG00000265873.1","gene_symbol":"MIR4289","gene_name":"microRNA 4289 [Source:HGNC Symbol;Acc:HGNC:38278]","synonyms":"hsa-mir-4289","biotype":"miRNA","ncbi_id":"100423015","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88745836,"end":88745905,"strand":-1,"description":"microRNA 4289 [Source:HGNC Symbol;Acc:HGNC:38278]"}, {"versioned_ensembl_gene_id":"ENSG00000206602.1","gene_symbol":"SNORD58A","gene_name":"small nucleolar RNA, C/D box 58A [Source:HGNC Symbol;Acc:HGNC:10208]","synonyms":"U58a,RNU58A","biotype":"snoRNA","ncbi_id":"26791","summary":null,"start":49491283,"end":49491347,"strand":-1,"description":"small nucleolar RNA, C/D box 58A [Source:HGNC Symbol;Acc:HGNC:10208]"}, {"versioned_ensembl_gene_id":"ENSG00000221771.1","gene_symbol":"MIR1205","gene_name":"microRNA 1205 [Source:HGNC Symbol;Acc:HGNC:35271]","synonyms":"MIRN1205,hsa-mir-1205","biotype":"miRNA","ncbi_id":"100302161","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127960633,"end":127960695,"strand":1,"description":"microRNA 1205 [Source:HGNC Symbol;Acc:HGNC:35271]"}, {"versioned_ensembl_gene_id":"ENSG00000275069.1","gene_symbol":"GNAS-AS1_5","gene_name":"GNAS antisense RNA 1 conserved region 5 [Source:RFAM;Acc:RF02131]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58850783,"end":58850903,"strand":1,"description":"GNAS antisense RNA 1 conserved region 5 [Source:RFAM;Acc:RF02131]"}, {"versioned_ensembl_gene_id":"ENSG00000194717.4","gene_symbol":"MIR494","gene_name":"microRNA 494 [Source:HGNC Symbol;Acc:HGNC:32084]","synonyms":"MIRN494,hsa-mir-494","biotype":"miRNA","ncbi_id":"574452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101029634,"end":101029714,"strand":1,"description":"microRNA 494 [Source:HGNC Symbol;Acc:HGNC:32084]"}, {"versioned_ensembl_gene_id":"ENSG00000263974.2","gene_symbol":"RN7SL121P","gene_name":"RNA, 7SL, cytoplasmic 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:46137]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479265","summary":null,"start":2595019,"end":2595291,"strand":-1,"description":"RNA, 7SL, cytoplasmic 121, pseudogene [Source:HGNC Symbol;Acc:HGNC:46137]"}, {"versioned_ensembl_gene_id":"ENSG00000253119.1","gene_symbol":"HNRNPA3P7","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421357","summary":null,"start":154337471,"end":154338452,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48496]"}, {"versioned_ensembl_gene_id":"ENSG00000215372.6","gene_symbol":"ZNF705G","gene_name":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131980","summary":null,"start":7355517,"end":7385558,"strand":-1,"description":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]"}, {"versioned_ensembl_gene_id":"ENSG00000264483.1","gene_symbol":"MIR5008","gene_name":"microRNA 5008 [Source:HGNC Symbol;Acc:HGNC:43546]","synonyms":"hsa-mir-5008","biotype":"miRNA","ncbi_id":"100847072","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":227941590,"end":227941683,"strand":-1,"description":"microRNA 5008 [Source:HGNC Symbol;Acc:HGNC:43546]"}, {"versioned_ensembl_gene_id":"ENSG00000264747.1","gene_symbol":"MIR3924","gene_name":"microRNA 3924 [Source:HGNC Symbol;Acc:HGNC:38984]","synonyms":"hsa-mir-3924","biotype":"miRNA","ncbi_id":"100500834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57304479,"end":57304559,"strand":-1,"description":"microRNA 3924 [Source:HGNC Symbol;Acc:HGNC:38984]"}, {"versioned_ensembl_gene_id":"ENSG00000200755.1","gene_symbol":"RNA5SP68","gene_name":"RNA, 5S ribosomal pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:42845]","synonyms":"RN5S68","biotype":"rRNA","ncbi_id":"100873303","summary":null,"start":173969318,"end":173969436,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:42845]"}, {"versioned_ensembl_gene_id":"ENSG00000206870.1","gene_symbol":"RNU6-398P","gene_name":"RNA, U6 small nuclear 398, pseudogene [Source:HGNC Symbol;Acc:HGNC:47361]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479742","summary":null,"start":60974327,"end":60974435,"strand":1,"description":"RNA, U6 small nuclear 398, pseudogene [Source:HGNC Symbol;Acc:HGNC:47361]"}, {"versioned_ensembl_gene_id":"ENSG00000212413.1","gene_symbol":"RNU11-3P","gene_name":"RNA, U11 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:46943]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479562","summary":null,"start":103312436,"end":103312568,"strand":-1,"description":"RNA, U11 small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:46943]"}, {"versioned_ensembl_gene_id":"ENSG00000212219.1","gene_symbol":"RNU6-604P","gene_name":"RNA, U6 small nuclear 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:47567]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479833","summary":null,"start":151900275,"end":151900374,"strand":1,"description":"RNA, U6 small nuclear 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:47567]"}, {"versioned_ensembl_gene_id":"ENSG00000275283.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":14938852,"end":14938951,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201672.1","gene_symbol":"SNORD113-4","gene_name":"small nucleolar RNA, C/D box 113-4 [Source:HGNC Symbol;Acc:HGNC:32983]","synonyms":"14q(I-4)","biotype":"snoRNA","ncbi_id":"767564","summary":null,"start":100936491,"end":100936565,"strand":1,"description":"small nucleolar RNA, C/D box 113-4 [Source:HGNC Symbol;Acc:HGNC:32983]"}, {"versioned_ensembl_gene_id":"ENSG00000212409.1","gene_symbol":"RNY4P18","gene_name":"RNA, Ro-associated Y4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:34068]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379298","summary":null,"start":111097325,"end":111097413,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:34068]"}, {"versioned_ensembl_gene_id":"ENSG00000202273.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6212638,"end":6212740,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201789.1","gene_symbol":"RNU6-1071P","gene_name":"RNA, U6 small nuclear 1071, pseudogene [Source:HGNC Symbol;Acc:HGNC:48034]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481517","summary":null,"start":146288596,"end":146288696,"strand":1,"description":"RNA, U6 small nuclear 1071, pseudogene [Source:HGNC Symbol;Acc:HGNC:48034]"}, {"versioned_ensembl_gene_id":"ENSG00000266751.1","gene_symbol":"MIR3661","gene_name":"microRNA 3661 [Source:HGNC Symbol;Acc:HGNC:38892]","synonyms":"hsa-mir-3661","biotype":"miRNA","ncbi_id":"100500905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134225757,"end":134225852,"strand":1,"description":"microRNA 3661 [Source:HGNC Symbol;Acc:HGNC:38892]"}, {"versioned_ensembl_gene_id":"ENSG00000238750.1","gene_symbol":"RNU7-27P","gene_name":"RNA, U7 small nuclear 27 pseudogene [Source:HGNC Symbol;Acc:HGNC:34123]","synonyms":"U7.27","biotype":"snRNA","ncbi_id":"100147814","summary":null,"start":128344081,"end":128344142,"strand":1,"description":"RNA, U7 small nuclear 27 pseudogene [Source:HGNC Symbol;Acc:HGNC:34123]"}, {"versioned_ensembl_gene_id":"ENSG00000252660.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62935701,"end":62935802,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222686.1","gene_symbol":"RNU4-72P","gene_name":"RNA, U4 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:47008]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479591","summary":null,"start":85751581,"end":85751753,"strand":1,"description":"RNA, U4 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:47008]"}, {"versioned_ensembl_gene_id":"ENSG00000241789.3","gene_symbol":"RN7SL504P","gene_name":"RNA, 7SL, cytoplasmic 504, pseudogene [Source:HGNC Symbol;Acc:HGNC:46520]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480515","summary":null,"start":51872178,"end":51872464,"strand":1,"description":"RNA, 7SL, cytoplasmic 504, pseudogene [Source:HGNC Symbol;Acc:HGNC:46520]"}, {"versioned_ensembl_gene_id":"ENSG00000252417.1","gene_symbol":"RNU7-179P","gene_name":"RNA, U7 small nuclear 179 pseudogene [Source:HGNC Symbol;Acc:HGNC:45713]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479092","summary":null,"start":15608078,"end":15608145,"strand":-1,"description":"RNA, U7 small nuclear 179 pseudogene [Source:HGNC Symbol;Acc:HGNC:45713]"}, {"versioned_ensembl_gene_id":"ENSG00000266619.1","gene_symbol":"MIR4642","gene_name":"microRNA 4642 [Source:HGNC Symbol;Acc:HGNC:41865]","synonyms":"hsa-mir-4642","biotype":"miRNA","ncbi_id":"100616352","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44435641,"end":44435722,"strand":1,"description":"microRNA 4642 [Source:HGNC Symbol;Acc:HGNC:41865]"}, {"versioned_ensembl_gene_id":"ENSG00000199719.1","gene_symbol":"RN7SKP74","gene_name":"RNA, 7SK small nuclear pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:45798]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479127","summary":null,"start":18295143,"end":18295451,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:45798]"}, {"versioned_ensembl_gene_id":"ENSG00000263834.1","gene_symbol":"MIR4635","gene_name":"microRNA 4635 [Source:HGNC Symbol;Acc:HGNC:41748]","synonyms":"hsa-mir-4635","biotype":"miRNA","ncbi_id":"100616479","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1062896,"end":1062974,"strand":-1,"description":"microRNA 4635 [Source:HGNC Symbol;Acc:HGNC:41748]"}, {"versioned_ensembl_gene_id":"ENSG00000201544.1","gene_symbol":"SNORA16B","gene_name":"small nucleolar RNA, H/ACA box 16B [Source:HGNC Symbol;Acc:HGNC:32606]","synonyms":"U98b","biotype":"snoRNA","ncbi_id":"692157","summary":null,"start":212352816,"end":212352950,"strand":1,"description":"small nucleolar RNA, H/ACA box 16B [Source:HGNC Symbol;Acc:HGNC:32606]"}, {"versioned_ensembl_gene_id":"ENSG00000278333.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85613017,"end":85613186,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000284436.1","gene_symbol":"MIR6869","gene_name":"microRNA 6869 [Source:HGNC Symbol;Acc:HGNC:50056]","synonyms":"hsa-mir-6869","biotype":"miRNA","ncbi_id":"102465524","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1392900,"end":1392961,"strand":-1,"description":"microRNA 6869 [Source:HGNC Symbol;Acc:HGNC:50056]"}, {"versioned_ensembl_gene_id":"ENSG00000200108.1","gene_symbol":"RNU6-774P","gene_name":"RNA, U6 small nuclear 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:47737]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481425","summary":null,"start":84233657,"end":84233763,"strand":1,"description":"RNA, U6 small nuclear 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:47737]"}, {"versioned_ensembl_gene_id":"ENSG00000207734.1","gene_symbol":"MIR517A","gene_name":"microRNA 517a [Source:HGNC Symbol;Acc:HGNC:32111]","synonyms":"hsa-mir-517a,MIRN517A","biotype":"miRNA","ncbi_id":"574479","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53712268,"end":53712354,"strand":1,"description":"microRNA 517a [Source:HGNC Symbol;Acc:HGNC:32111]"}, {"versioned_ensembl_gene_id":"ENSG00000222663.1","gene_symbol":"RNU4-55P","gene_name":"RNA, U4 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46991]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481189","summary":null,"start":105824634,"end":105824770,"strand":1,"description":"RNA, U4 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46991]"}, {"versioned_ensembl_gene_id":"ENSG00000278670.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55019324,"end":55043883,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000252370.1","gene_symbol":"RNA5SP438","gene_name":"RNA, 5S ribosomal pseudogene 438 [Source:HGNC Symbol;Acc:HGNC:43338]","synonyms":"RN5S438","biotype":"rRNA","ncbi_id":"100873687","summary":null,"start":34120056,"end":34120167,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 438 [Source:HGNC Symbol;Acc:HGNC:43338]"}, {"versioned_ensembl_gene_id":"ENSG00000263638.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31747708,"end":31747810,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000266195.2","gene_symbol":"RN7SL163P","gene_name":"RNA, 7SL, cytoplasmic 163, pseudogene [Source:HGNC Symbol;Acc:HGNC:46179]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479280","summary":null,"start":17506453,"end":17506728,"strand":1,"description":"RNA, 7SL, cytoplasmic 163, pseudogene [Source:HGNC Symbol;Acc:HGNC:46179]"}, {"versioned_ensembl_gene_id":"ENSG00000242256.3","gene_symbol":"RN7SL57P","gene_name":"RNA, 7SL, cytoplasmic 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46073]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480484","summary":null,"start":112242550,"end":112242839,"strand":-1,"description":"RNA, 7SL, cytoplasmic 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46073]"}, {"versioned_ensembl_gene_id":"ENSG00000252758.1","gene_symbol":"RNU6-445P","gene_name":"RNA, U6 small nuclear 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:47408]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479763","summary":null,"start":74857675,"end":74857781,"strand":1,"description":"RNA, U6 small nuclear 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:47408]"}, {"versioned_ensembl_gene_id":"ENSG00000207775.1","gene_symbol":"MIR548A1","gene_name":"microRNA 548a-1 [Source:HGNC Symbol;Acc:HGNC:32796]","synonyms":"MIRN548A1,hsa-mir-548a-1","biotype":"miRNA","ncbi_id":"693125","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18571784,"end":18571880,"strand":1,"description":"microRNA 548a-1 [Source:HGNC Symbol;Acc:HGNC:32796]"}, {"versioned_ensembl_gene_id":"ENSG00000229005.2","gene_symbol":"HNF4A-AS1","gene_name":"HNF4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49505]","synonyms":"uc002xlx","biotype":"antisense_RNA","ncbi_id":"101927219","summary":null,"start":44372746,"end":44395706,"strand":-1,"description":"HNF4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49505]"}, {"versioned_ensembl_gene_id":"ENSG00000229415.9","gene_symbol":"SFTA3","gene_name":"surfactant associated 3 [Source:HGNC Symbol;Acc:HGNC:18387]","synonyms":"SP-H,SFTPH,NANCI,SFTPH,NANCI","biotype":"protein_coding","ncbi_id":"253970","summary":null,"start":36473288,"end":36513829,"strand":-1,"description":"surfactant associated 3 [Source:HGNC Symbol;Acc:HGNC:18387]"}, {"versioned_ensembl_gene_id":"ENSG00000207825.1","gene_symbol":"MIR519B","gene_name":"microRNA 519b [Source:HGNC Symbol;Acc:HGNC:32101]","synonyms":"MIRN519B,hsa-mir-519b","biotype":"miRNA","ncbi_id":"574469","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53695213,"end":53695293,"strand":1,"description":"microRNA 519b [Source:HGNC Symbol;Acc:HGNC:32101]"}, {"versioned_ensembl_gene_id":"ENSG00000207946.3","gene_symbol":"MIR516B1","gene_name":"microRNA 516b-1 [Source:HGNC Symbol;Acc:HGNC:32122]","synonyms":"MIRN516B1,MIRN516-4,hsa-mir-516b-1,hsa-mir-516-4","biotype":"miRNA","ncbi_id":"574490","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53736845,"end":53736934,"strand":1,"description":"microRNA 516b-1 [Source:HGNC Symbol;Acc:HGNC:32122]"}, {"versioned_ensembl_gene_id":"ENSG00000207942.2","gene_symbol":"MIR136","gene_name":"microRNA 136 [Source:HGNC Symbol;Acc:HGNC:31522]","synonyms":"MIRN136,hsa-mir-136","biotype":"miRNA","ncbi_id":"406927","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100884702,"end":100884783,"strand":1,"description":"microRNA 136 [Source:HGNC Symbol;Acc:HGNC:31522]"}, {"versioned_ensembl_gene_id":"ENSG00000207361.1","gene_symbol":"RNU6-178P","gene_name":"RNA, U6 small nuclear 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:47141]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479645","summary":null,"start":28416448,"end":28416551,"strand":1,"description":"RNA, U6 small nuclear 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:47141]"}, {"versioned_ensembl_gene_id":"ENSG00000252618.1","gene_symbol":"RNA5SP441","gene_name":"RNA, 5S ribosomal pseudogene 441 [Source:HGNC Symbol;Acc:HGNC:43341]","synonyms":"RN5S441","biotype":"rRNA","ncbi_id":"100873689","summary":null,"start":40374089,"end":40374176,"strand":1,"description":"RNA, 5S ribosomal pseudogene 441 [Source:HGNC Symbol;Acc:HGNC:43341]"}, {"versioned_ensembl_gene_id":"ENSG00000251748.1","gene_symbol":"RNU4ATAC11P","gene_name":"RNA, U4atac small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46897]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481158","summary":null,"start":33868540,"end":33868665,"strand":1,"description":"RNA, U4atac small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46897]"}, {"versioned_ensembl_gene_id":"ENSG00000239820.3","gene_symbol":"RN7SL213P","gene_name":"RNA, 7SL, cytoplasmic 213, pseudogene [Source:HGNC Symbol;Acc:HGNC:46229]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480979","summary":null,"start":67751228,"end":67751544,"strand":-1,"description":"RNA, 7SL, cytoplasmic 213, pseudogene [Source:HGNC Symbol;Acc:HGNC:46229]"}, {"versioned_ensembl_gene_id":"ENSG00000251952.1","gene_symbol":"RNU6-1219P","gene_name":"RNA, U6 small nuclear 1219, pseudogene [Source:HGNC Symbol;Acc:HGNC:48182]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480649","summary":null,"start":29191697,"end":29191808,"strand":-1,"description":"RNA, U6 small nuclear 1219, pseudogene [Source:HGNC Symbol;Acc:HGNC:48182]"}, {"versioned_ensembl_gene_id":"ENSG00000222428.1","gene_symbol":"RNA5SP231","gene_name":"RNA, 5S ribosomal pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:43131]","synonyms":"RN5S231","biotype":"rRNA","ncbi_id":"100873489","summary":null,"start":68723911,"end":68724048,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:43131]"}, {"versioned_ensembl_gene_id":"ENSG00000200680.1","gene_symbol":"SNORD115-4","gene_name":"small nucleolar RNA, C/D box 115-4 [Source:HGNC Symbol;Acc:HGNC:33023]","synonyms":"HBII-52-4","biotype":"snoRNA","ncbi_id":"100033441","summary":null,"start":25176832,"end":25176913,"strand":1,"description":"small nucleolar RNA, C/D box 115-4 [Source:HGNC Symbol;Acc:HGNC:33023]"}, {"versioned_ensembl_gene_id":"ENSG00000212455.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":18040606,"end":18040733,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000199562.1","gene_symbol":"RNU6-37P","gene_name":"RNA, U6 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:34281]","synonyms":"RNU6-37","biotype":"snRNA","ncbi_id":"106478920","summary":null,"start":10298966,"end":10299072,"strand":1,"description":"RNA, U6 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:34281]"}, {"versioned_ensembl_gene_id":"ENSG00000277415.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30053279,"end":30053354,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000249020.1","gene_symbol":"SNORA58","gene_name":"small nucleolar RNA, H/ACA box 58 [Source:HGNC Symbol;Acc:HGNC:32652]","synonyms":"SNORA58B,ACA58","biotype":"snoRNA","ncbi_id":"677836","summary":null,"start":131479097,"end":131479233,"strand":-1,"description":"small nucleolar RNA, H/ACA box 58 [Source:HGNC Symbol;Acc:HGNC:32652]"}, {"versioned_ensembl_gene_id":"ENSG00000277771.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49846456,"end":49846720,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000221187.1","gene_symbol":"MIR548M","gene_name":"microRNA 548m [Source:HGNC Symbol;Acc:HGNC:35331]","synonyms":"MIRN548M,hsa-mir-548m","biotype":"miRNA","ncbi_id":"100313772","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95063141,"end":95063226,"strand":-1,"description":"microRNA 548m [Source:HGNC Symbol;Acc:HGNC:35331]"}, {"versioned_ensembl_gene_id":"ENSG00000275752.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54264578,"end":54264680,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000159915.12","gene_symbol":"ZNF233","gene_name":"zinc finger protein 233 [Source:HGNC Symbol;Acc:HGNC:30946]","synonyms":"FLJ38032","biotype":"protein_coding","ncbi_id":"353355","summary":null,"start":44259880,"end":44275317,"strand":1,"description":"zinc finger protein 233 [Source:HGNC Symbol;Acc:HGNC:30946]"}, {"versioned_ensembl_gene_id":"ENSG00000207816.1","gene_symbol":"MIR124-2","gene_name":"microRNA 124-2 [Source:HGNC Symbol;Acc:HGNC:31503]","synonyms":"MIRN124A2,MIRN124-2,hsa-mir-124a-2,hsa-mir-124-2","biotype":"miRNA","ncbi_id":"406908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64379149,"end":64379257,"strand":1,"description":"microRNA 124-2 [Source:HGNC Symbol;Acc:HGNC:31503]"}, {"versioned_ensembl_gene_id":"ENSG00000263575.1","gene_symbol":"MIR4665","gene_name":"microRNA 4665 [Source:HGNC Symbol;Acc:HGNC:41696]","synonyms":"hsa-mir-4665","biotype":"miRNA","ncbi_id":"100616288","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6007826,"end":6007904,"strand":1,"description":"microRNA 4665 [Source:HGNC Symbol;Acc:HGNC:41696]"}, {"versioned_ensembl_gene_id":"ENSG00000263573.1","gene_symbol":"MIR4270","gene_name":"microRNA 4270 [Source:HGNC Symbol;Acc:HGNC:38377]","synonyms":"hsa-mir-4270","biotype":"miRNA","ncbi_id":"100422868","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15496239,"end":15496308,"strand":-1,"description":"microRNA 4270 [Source:HGNC Symbol;Acc:HGNC:38377]"}, {"versioned_ensembl_gene_id":"ENSG00000275803.1","gene_symbol":"RN7SL736P","gene_name":"RNA, 7SL, cytoplasmic 736, pseudogene [Source:HGNC Symbol;Acc:HGNC:46752]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080652","summary":null,"start":90293939,"end":90294207,"strand":1,"description":"RNA, 7SL, cytoplasmic 736, pseudogene [Source:HGNC Symbol;Acc:HGNC:46752]"}, {"versioned_ensembl_gene_id":"ENSG00000207987.1","gene_symbol":"MIR518E","gene_name":"microRNA 518e [Source:HGNC Symbol;Acc:HGNC:32119]","synonyms":"MIRN518E,hsa-mir-518e","biotype":"miRNA","ncbi_id":"574487","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53729838,"end":53729925,"strand":1,"description":"microRNA 518e [Source:HGNC Symbol;Acc:HGNC:32119]"}, {"versioned_ensembl_gene_id":"ENSG00000264089.1","gene_symbol":"MIR3681","gene_name":"microRNA 3681 [Source:HGNC Symbol;Acc:HGNC:38994]","synonyms":"hsa-mir-3681","biotype":"miRNA","ncbi_id":"100500884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12199130,"end":12199201,"strand":1,"description":"microRNA 3681 [Source:HGNC Symbol;Acc:HGNC:38994]"}, {"versioned_ensembl_gene_id":"ENSG00000276181.1","gene_symbol":"MIR6794","gene_name":"microRNA 6794 [Source:HGNC Symbol;Acc:HGNC:50117]","synonyms":"hsa-mir-6794","biotype":"miRNA","ncbi_id":"102466196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12852260,"end":12852327,"strand":1,"description":"microRNA 6794 [Source:HGNC Symbol;Acc:HGNC:50117]"}, {"versioned_ensembl_gene_id":"ENSG00000230076.1","gene_symbol":"RPL10P6","gene_name":"ribosomal protein L10 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285176","summary":null,"start":214847128,"end":214847445,"strand":1,"description":"ribosomal protein L10 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52343]"}, {"versioned_ensembl_gene_id":"ENSG00000184659.5","gene_symbol":"FOXD4L4","gene_name":"forkhead box D4 like 4 [Source:HGNC Symbol;Acc:HGNC:23762]","synonyms":"OTTHUMG00000013337,FOXD4L2,bA460E7.2,OTTHUMG00000066752","biotype":"protein_coding","ncbi_id":"349334","summary":null,"start":65736555,"end":65738784,"strand":1,"description":"forkhead box D4 like 4 [Source:HGNC Symbol;Acc:HGNC:23762]"}, {"versioned_ensembl_gene_id":"ENSG00000280103.1","gene_symbol":"AC007792.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3355554,"end":3355955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278098.1","gene_symbol":"MIR7973-1","gene_name":"microRNA 7973-1 [Source:HGNC Symbol;Acc:HGNC:50040]","synonyms":"hsa-mir-7973-1","biotype":"miRNA","ncbi_id":"102466250","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51314034,"end":51314109,"strand":1,"description":"microRNA 7973-1 [Source:HGNC Symbol;Acc:HGNC:50040]"}, {"versioned_ensembl_gene_id":"ENSG00000258577.1","gene_symbol":"SNRPGP1","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20033]","synonyms":"SNRPGP","biotype":"processed_pseudogene","ncbi_id":"326272","summary":null,"start":50571919,"end":50572140,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20033]"}, {"versioned_ensembl_gene_id":"ENSG00000283879.1","gene_symbol":"AC132825.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22519195,"end":22519504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255870.1","gene_symbol":"AP003170.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113789242,"end":113790027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283045.1","gene_symbol":"AC103703.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44486153,"end":44486815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250668.1","gene_symbol":"LINC02123","gene_name":"long intergenic non-protein coding RNA 2123 [Source:HGNC Symbol;Acc:HGNC:52980]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929261","summary":null,"start":7346986,"end":7347977,"strand":-1,"description":"long intergenic non-protein coding RNA 2123 [Source:HGNC Symbol;Acc:HGNC:52980]"}, {"versioned_ensembl_gene_id":"ENSG00000248775.1","gene_symbol":"AC091951.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7287924,"end":7288477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090612.20","gene_symbol":"ZNF268","gene_name":"zinc finger protein 268 [Source:HGNC Symbol;Acc:HGNC:13061]","synonyms":"HZF3","biotype":"protein_coding","ncbi_id":"10795","summary":null,"start":133181409,"end":133214831,"strand":1,"description":"zinc finger protein 268 [Source:HGNC Symbol;Acc:HGNC:13061]"}, {"versioned_ensembl_gene_id":"ENSG00000256825.4","gene_symbol":"AC026786.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":133130984,"end":133202369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130720.12","gene_symbol":"FIBCD1","gene_name":"fibrinogen C domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25922]","synonyms":"FLJ14810","biotype":"protein_coding","ncbi_id":"84929","summary":"FIBCD1 is a conserved type II transmembrane endocytic receptor that binds chitin and is located primarily in the intestinal brush border (Schlosser et al., 2009 [PubMed 19710473]).[supplied by OMIM, Apr 2010]","start":130902438,"end":130939286,"strand":-1,"description":"fibrinogen C domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25922]"}, {"versioned_ensembl_gene_id":"ENSG00000173914.11","gene_symbol":"RBM4B","gene_name":"RNA binding motif protein 4B [Source:HGNC Symbol;Acc:HGNC:28842]","synonyms":"ZCRB3B,ZCCHC21B,ZCCHC15,RBM4L,RBM30,MGC10871","biotype":"protein_coding","ncbi_id":"83759","summary":null,"start":66664998,"end":66677921,"strand":-1,"description":"RNA binding motif protein 4B [Source:HGNC Symbol;Acc:HGNC:28842]"}, {"versioned_ensembl_gene_id":"ENSG00000066027.11","gene_symbol":"PPP2R5A","gene_name":"protein phosphatase 2 regulatory subunit B'alpha [Source:HGNC Symbol;Acc:HGNC:9309]","synonyms":"B56alpha,B56A,PR61A","biotype":"protein_coding","ncbi_id":"5525","summary":"The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an alpha isoform of the regulatory subunit B56 subfamily. Alternative transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":212285537,"end":212361863,"strand":1,"description":"protein phosphatase 2 regulatory subunit B'alpha [Source:HGNC Symbol;Acc:HGNC:9309]"}, {"versioned_ensembl_gene_id":"ENSG00000184154.13","gene_symbol":"LRTOMT","gene_name":"leucine rich transmembrane and O-methyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:25033]","synonyms":"CFAP111,LRRC51,DFNB63,COMT2","biotype":"protein_coding","ncbi_id":"220074","summary":"This locus represents naturally occurring readthrough transcription between the neighboring LRRC51 (leucine-rich repeat containing 51) and TOMT (transmembrane O-methyltransferase) genes on chromosome 11. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. Multiple reports implicate mutations in this gene in nonsyndromic deafness.[provided by RefSeq, Feb 2021]","start":72080331,"end":72110782,"strand":1,"description":"leucine rich transmembrane and O-methyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:25033]"}, {"versioned_ensembl_gene_id":"ENSG00000165060.11","gene_symbol":"FXN","gene_name":"frataxin [Source:HGNC Symbol;Acc:HGNC:3951]","synonyms":"X25,FRDA,FARR,FA,CyaY","biotype":"protein_coding","ncbi_id":"2395","summary":"This nuclear gene encodes a mitochondrial protein which belongs to the FRATAXIN family. The protein functions in regulating mitochondrial iron transport and respiration. The expansion of intronic trinucleotide repeat GAA from 8-33 repeats to >90 repeats results in Friedreich ataxia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":69035259,"end":69100178,"strand":1,"description":"frataxin [Source:HGNC Symbol;Acc:HGNC:3951]"}, {"versioned_ensembl_gene_id":"ENSG00000127152.17","gene_symbol":"BCL11B","gene_name":"B-cell CLL/lymphoma 11B [Source:HGNC Symbol;Acc:HGNC:13222]","synonyms":"CTIP-2,ZNF856B,hRIT1-alpha,CTIP2","biotype":"protein_coding","ncbi_id":"64919","summary":"This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":99169287,"end":99271524,"strand":-1,"description":"B-cell CLL/lymphoma 11B [Source:HGNC Symbol;Acc:HGNC:13222]"}, {"versioned_ensembl_gene_id":"ENSG00000248930.1","gene_symbol":"AC020893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73020700,"end":73021279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251467.1","gene_symbol":"AC020893.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72996920,"end":72997642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265916.1","gene_symbol":"AC015818.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20532248,"end":20532881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278456.1","gene_symbol":"AC015712.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100888472,"end":100889106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273189.1","gene_symbol":"AC010619.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":49474586,"end":49487637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262098.1","gene_symbol":"AC127496.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81023545,"end":81025503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259579.1","gene_symbol":"AC087762.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100716249,"end":100828497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242199.1","gene_symbol":"AC022336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124733418,"end":124733754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083097.14","gene_symbol":"DOPEY1","gene_name":"dopey family member 1 [Source:HGNC Symbol;Acc:HGNC:21194]","synonyms":"KIAA1117,dJ202D23.2","biotype":"protein_coding","ncbi_id":"23033","summary":null,"start":83067666,"end":83171350,"strand":1,"description":"dopey family member 1 [Source:HGNC Symbol;Acc:HGNC:21194]"}, {"versioned_ensembl_gene_id":"ENSG00000165501.16","gene_symbol":"LRR1","gene_name":"leucine rich repeat protein 1 [Source:HGNC Symbol;Acc:HGNC:19742]","synonyms":"PPIL5,MGC20689,LRR-1","biotype":"protein_coding","ncbi_id":"122769","summary":"The protein encoded by this gene contains a leucine-rich repeat (LRR). It specifically interacts with TNFRSF9/4-1BB, a member of the tumor necrosis factor receptor (TNFR) superfamily. Overexpression of this gene suppresses the activation of NF-kappa B induced by TNFRSF9 or TNF receptor-associated factor 2 (TRAF2), which suggests that this protein is a negative regulator of TNFRSF9-mediated signaling cascades. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]","start":49598697,"end":49614672,"strand":1,"description":"leucine rich repeat protein 1 [Source:HGNC Symbol;Acc:HGNC:19742]"}, {"versioned_ensembl_gene_id":"ENSG00000281928.1","gene_symbol":"AC247036.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106207374,"end":106209342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013375.15","gene_symbol":"PGM3","gene_name":"phosphoglucomutase 3 [Source:HGNC Symbol;Acc:HGNC:8907]","synonyms":"PAGM,DKFZP434B187,AGM1","biotype":"protein_coding","ncbi_id":"5238","summary":"This gene encodes a member of the phosphohexose mutase family. The encoded protein mediates both glycogen formation and utilization by catalyzing the interconversion of glucose-1-phosphate and glucose-6-phosphate. A non-synonymous single nucleotide polymorphism in this gene may play a role in resistance to diabetic nephropathy and neuropathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":83161150,"end":83193936,"strand":-1,"description":"phosphoglucomutase 3 [Source:HGNC Symbol;Acc:HGNC:8907]"}, {"versioned_ensembl_gene_id":"ENSG00000260369.2","gene_symbol":"AC120024.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80453735,"end":80454729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258868.1","gene_symbol":"AL110505.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49057713,"end":49077505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107130.9","gene_symbol":"NCS1","gene_name":"neuronal calcium sensor 1 [Source:HGNC Symbol;Acc:HGNC:3953]","synonyms":"NCS-1,FREQ","biotype":"protein_coding","ncbi_id":"23413","summary":"This gene is a member of the neuronal calcium sensor gene family, which encode calcium-binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein-coupled receptor phosphorylation in a calcium-dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":130172578,"end":130237304,"strand":1,"description":"neuronal calcium sensor 1 [Source:HGNC Symbol;Acc:HGNC:3953]"}, {"versioned_ensembl_gene_id":"ENSG00000274137.2","gene_symbol":"MYOM2","gene_name":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9172","summary":"The giant protein titin, together with its associated proteins, interconnects the major structure of sarcomeres, the M bands and Z discs. The C-terminal end of the titin string extends into the M line, where it binds tightly to M-band constituents of apparent molecular masses of 190 kD and 165 kD. The predicted MYOM2 protein contains 1,465 amino acids. Like MYOM1, MYOM2 has a unique N-terminal domain followed by 12 repeat domains with strong homology to either fibronectin type III or immunoglobulin C2 domains. Protein sequence comparisons suggested that the MYOM2 protein and bovine M protein are identical. [provided by RefSeq, Jul 2008]","start":2044989,"end":2165303,"strand":1,"description":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]"}, {"versioned_ensembl_gene_id":"ENSG00000246394.7","gene_symbol":"AC073911.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133030389,"end":133037222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220804.8","gene_symbol":"LINC01881","gene_name":"long intergenic non-protein coding RNA 1881 [Source:HGNC Symbol;Acc:HGNC:52700]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728323","summary":null,"start":242088633,"end":242160153,"strand":1,"description":"long intergenic non-protein coding RNA 1881 [Source:HGNC Symbol;Acc:HGNC:52700]"}, {"versioned_ensembl_gene_id":"ENSG00000189423.11","gene_symbol":"USP32P3","gene_name":"ubiquitin specific peptidase 32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43576]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"347716","summary":null,"start":20415547,"end":20431008,"strand":1,"description":"ubiquitin specific peptidase 32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43576]"}, {"versioned_ensembl_gene_id":"ENSG00000224958.5","gene_symbol":"PGM5-AS1","gene_name":"PGM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44181]","synonyms":"FAM233A","biotype":"antisense_RNA","ncbi_id":"572558","summary":null,"start":68355189,"end":68357852,"strand":-1,"description":"PGM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44181]"}, {"versioned_ensembl_gene_id":"ENSG00000148358.19","gene_symbol":"GPR107","gene_name":"G protein-coupled receptor 107 [Source:HGNC Symbol;Acc:HGNC:17830]","synonyms":"RP11-88G17,LUSTR1,KIAA1624,FLJ20998","biotype":"protein_coding","ncbi_id":"57720","summary":null,"start":130053426,"end":130140169,"strand":1,"description":"G protein-coupled receptor 107 [Source:HGNC Symbol;Acc:HGNC:17830]"}, {"versioned_ensembl_gene_id":"ENSG00000233178.7","gene_symbol":"AL161457.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68393881,"end":68406500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273466.1","gene_symbol":"AC012510.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":218633256,"end":218634014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132716.18","gene_symbol":"DCAF8","gene_name":"DDB1 and CUL4 associated factor 8 [Source:HGNC Symbol;Acc:HGNC:24891]","synonyms":"WDR42A,H326,FLJ35857","biotype":"protein_coding","ncbi_id":"50717","summary":"This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2009]","start":160215715,"end":160262531,"strand":-1,"description":"DDB1 and CUL4 associated factor 8 [Source:HGNC Symbol;Acc:HGNC:24891]"}, {"versioned_ensembl_gene_id":"ENSG00000282191.1","gene_symbol":"AC125453.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2033484,"end":2039347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248371.5","gene_symbol":"LINC02056","gene_name":"long intergenic non-protein coding RNA 2056 [Source:HGNC Symbol;Acc:HGNC:52898]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102477328","summary":null,"start":72574120,"end":72660669,"strand":-1,"description":"long intergenic non-protein coding RNA 2056 [Source:HGNC Symbol;Acc:HGNC:52898]"}, {"versioned_ensembl_gene_id":"ENSG00000261120.1","gene_symbol":"AL133299.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59919423,"end":59920339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037757.13","gene_symbol":"MRI1","gene_name":"methylthioribose-1-phosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:28469]","synonyms":"mtnA,MRDI,MGC3207,Ypr118w","biotype":"protein_coding","ncbi_id":"84245","summary":"This enzyme functions in the methionine salvage pathway by catalyzing the interconversion of methylthioribose-1-phosphate and methythioribulose-1-phosphate. Elevated expression of the encoded protein is associated with metastatic melanoma and this protein promotes melanoma cell invasion independent of its enzymatic activity. Mutations in this gene may be associated with vanishing white matter disease (VMWD). [provided by RefSeq, Jul 2016]","start":13764532,"end":13774282,"strand":1,"description":"methylthioribose-1-phosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:28469]"}, {"versioned_ensembl_gene_id":"ENSG00000150779.11","gene_symbol":"TIMM8B","gene_name":"translocase of inner mitochondrial membrane 8 homolog B [Source:HGNC Symbol;Acc:HGNC:11818]","synonyms":"TIM8B,MGC117373,MGC102866,FLJ21744,DDP2","biotype":"protein_coding","ncbi_id":"26521","summary":"This gene encodes a member of a well-conserved family of proteins with similarity to yeast Tim mitochondrial import proteins. This gene is encoded by a nuclear gene and is transported into the intermembrane space of the mitochondrion. When formed into complexes, these proteins guide membrane-spanning proteins across the mitochondrial intermembrane space before they are added into the mitochondrial inner membrane. This gene is adjacent to succinate dehydrogenase, subunit D (SDHD), in which mutations have been found in affected members of families with hereditary paraganglioma.[provided by RefSeq, Aug 2009]","start":112084800,"end":112086798,"strand":-1,"description":"translocase of inner mitochondrial membrane 8 homolog B [Source:HGNC Symbol;Acc:HGNC:11818]"}, {"versioned_ensembl_gene_id":"ENSG00000099341.11","gene_symbol":"PSMD8","gene_name":"proteasome 26S subunit, non-ATPase 8 [Source:HGNC Symbol;Acc:HGNC:9566]","synonyms":"p31,Nin1p,HYPF,HIP6,S14,Rpn12","biotype":"protein_coding","ncbi_id":"5714","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. A pseudogene has been identified on chromosome 1. [provided by RefSeq, Jul 2008]","start":38374536,"end":38383824,"strand":1,"description":"proteasome 26S subunit, non-ATPase 8 [Source:HGNC Symbol;Acc:HGNC:9566]"}, {"versioned_ensembl_gene_id":"ENSG00000274305.4","gene_symbol":"LENG8","gene_name":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]","synonyms":"pp13842,MGC40108,KIAA1932","biotype":"protein_coding","ncbi_id":"114823","summary":null,"start":54379038,"end":54392337,"strand":1,"description":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]"}, {"versioned_ensembl_gene_id":"ENSG00000258605.1","gene_symbol":"DYNLL1P2","gene_name":"dynein light chain LC8-type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20724]","synonyms":"DNCL1P2","biotype":"processed_pseudogene","ncbi_id":"731308","summary":null,"start":81412970,"end":81413239,"strand":1,"description":"dynein light chain LC8-type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20724]"}, {"versioned_ensembl_gene_id":"ENSG00000204370.9","gene_symbol":"SDHD","gene_name":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]","synonyms":"cybS,PGL1,PGL","biotype":"protein_coding","ncbi_id":"6392","summary":"This gene encodes a member of complex II of the respiratory chain, which is responsible for the oxidation of succinate. The encoded protein is one of two integral membrane proteins anchoring the complex to the matrix side of the mitochondrial inner membrane. Mutations in this gene are associated with the formation of tumors, including hereditary paraganglioma. Transmission of disease occurs almost exclusively through the paternal allele, suggesting that this locus may be maternally imprinted. There are pseudogenes for this gene on chromosomes 1, 2, 3, 7, and 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":112086773,"end":112120013,"strand":1,"description":"succinate dehydrogenase complex subunit D [Source:HGNC Symbol;Acc:HGNC:10683]"}, {"versioned_ensembl_gene_id":"ENSG00000214264.4","gene_symbol":"KCTD9P4","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422242","summary":null,"start":112180773,"end":112183191,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49913]"}, {"versioned_ensembl_gene_id":"ENSG00000101331.15","gene_symbol":"CCM2L","gene_name":"CCM2 like scaffolding protein [Source:HGNC Symbol;Acc:HGNC:16153]","synonyms":"dJ310O13.5,C20orf160","biotype":"protein_coding","ncbi_id":"140706","summary":null,"start":32010450,"end":32032180,"strand":1,"description":"CCM2 like scaffolding protein [Source:HGNC Symbol;Acc:HGNC:16153]"}, {"versioned_ensembl_gene_id":"ENSG00000263494.1","gene_symbol":"AC004702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20185082,"end":20322973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173918.14","gene_symbol":"C1QTNF1","gene_name":"C1q and TNF related 1 [Source:HGNC Symbol;Acc:HGNC:14324]","synonyms":"FLJ90694,CTRP1,ZSIG37,GIP","biotype":"protein_coding","ncbi_id":"114897","summary":null,"start":79022814,"end":79049788,"strand":1,"description":"C1q and TNF related 1 [Source:HGNC Symbol;Acc:HGNC:14324]"}, {"versioned_ensembl_gene_id":"ENSG00000254638.1","gene_symbol":"AP002884.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112165197,"end":112172606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136827.11","gene_symbol":"TOR1A","gene_name":"torsin family 1 member A [Source:HGNC Symbol;Acc:HGNC:3098]","synonyms":"DYT1,DQ2","biotype":"protein_coding","ncbi_id":"1861","summary":"The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family and is expressed prominently in the substantia nigra pars compacta. Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1. [provided by RefSeq, Jul 2008]","start":129812944,"end":129824134,"strand":-1,"description":"torsin family 1 member A [Source:HGNC Symbol;Acc:HGNC:3098]"}, {"versioned_ensembl_gene_id":"ENSG00000254293.1","gene_symbol":"AC026688.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154483917,"end":154486150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262075.3","gene_symbol":"DKFZP434A062","gene_name":"uncharacterized LOC26102 [Source:NCBI gene;Acc:26102]","synonyms":null,"biotype":"lincRNA","ncbi_id":"26102","summary":null,"start":136322303,"end":136327323,"strand":-1,"description":"uncharacterized LOC26102 [Source:NCBI gene;Acc:26102]"}, {"versioned_ensembl_gene_id":"ENSG00000259381.2","gene_symbol":"AC090695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100645434,"end":100646655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156345.17","gene_symbol":"CDK20","gene_name":"cyclin dependent kinase 20 [Source:HGNC Symbol;Acc:HGNC:21420]","synonyms":"p42,CCRK","biotype":"protein_coding","ncbi_id":"23552","summary":"The protein encoded by this gene contains a kinase domain most closely related to the cyclin-dependent protein kinases. The encoded kinase may activate cyclin-dependent kinase 2 and is involved in cell growth. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Dec 2009]","start":87966441,"end":87974753,"strand":-1,"description":"cyclin dependent kinase 20 [Source:HGNC Symbol;Acc:HGNC:21420]"}, {"versioned_ensembl_gene_id":"ENSG00000226355.1","gene_symbol":"AL353803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129438216,"end":129439118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267624.1","gene_symbol":"AC087645.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78211618,"end":78211908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284625.1","gene_symbol":"AP000867.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71639551,"end":71639769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126790.11","gene_symbol":"L3HYPDH","gene_name":"trans-L-3-hydroxyproline dehydratase [Source:HGNC Symbol;Acc:HGNC:20488]","synonyms":"C14orf149,FLJ25436","biotype":"protein_coding","ncbi_id":"112849","summary":"The protein encoded by this gene is a dehydratase that converts trans-3-hydroxy-L-proline to delta(1)-pyrroline-2-carboxylate. This enzyme may function to degrade dietary proteins that contain trans-3-hydroxy-L-proline as well as other proteins such as collagen IV. The encoded protein can be converted to an epimerase by changing a threonine to a cysteine at a catalytic site. [provided by RefSeq, Sep 2016]","start":59460363,"end":59484430,"strand":-1,"description":"trans-L-3-hydroxyproline dehydratase [Source:HGNC Symbol;Acc:HGNC:20488]"}, {"versioned_ensembl_gene_id":"ENSG00000254975.1","gene_symbol":"AP001189.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76675079,"end":76703195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136856.17","gene_symbol":"SLC2A8","gene_name":"solute carrier family 2 member 8 [Source:HGNC Symbol;Acc:HGNC:13812]","synonyms":"GLUTX1,GLUT8","biotype":"protein_coding","ncbi_id":"29988","summary":"This gene belongs to the solute carrier 2A family, which includes intracellular glucose transporters. Based on sequence comparison, the glucose transporters are grouped into three classes and this gene is a member of class II. The encoded protein, like other members of the family, contains several conserved residues and motifs and 12 transmembrane domains with both amino and carboxyl ends being on the cytosolic side of the membrane. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":127397138,"end":127408424,"strand":1,"description":"solute carrier family 2 member 8 [Source:HGNC Symbol;Acc:HGNC:13812]"}, {"versioned_ensembl_gene_id":"ENSG00000215795.2","gene_symbol":"AL390728.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247183813,"end":247185482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255605.1","gene_symbol":"AP000820.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95698086,"end":95700623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076356.6","gene_symbol":"PLXNA2","gene_name":"plexin A2 [Source:HGNC Symbol;Acc:HGNC:9100]","synonyms":"PLXN2,OCT,KIAA0463,FLJ30634,FLJ11751","biotype":"protein_coding","ncbi_id":"5362","summary":"This gene encodes a member of the plexin-A family of semaphorin co-receptors. Semaphorins are a large family of secreted or membrane-bound proteins that mediate repulsive effects on axon pathfinding during nervous system development. A subset of semaphorins are recognized by plexin-A/neuropilin transmembrane receptor complexes, triggering a cellular signal transduction cascade that leads to axon repulsion. This plexin-A family member is thought to transduce signals from semaphorin-3A and -3C. [provided by RefSeq, Jul 2008]","start":208022242,"end":208244320,"strand":-1,"description":"plexin A2 [Source:HGNC Symbol;Acc:HGNC:9100]"}, {"versioned_ensembl_gene_id":"ENSG00000261314.1","gene_symbol":"AC105275.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":211583015,"end":211583725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249387.1","gene_symbol":"KRTAP5-14P","gene_name":"keratin associated protein 5-14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23608]","synonyms":"KRTAP5P2,KRTAP5.P2","biotype":"processed_pseudogene","ncbi_id":"387276","summary":null,"start":71579728,"end":71579848,"strand":-1,"description":"keratin associated protein 5-14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23608]"}, {"versioned_ensembl_gene_id":"ENSG00000184055.4","gene_symbol":"OR7E87P","gene_name":"olfactory receptor family 7 subfamily E member 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:14709]","synonyms":"OR11-9,OR7F3P,OR7E3P","biotype":"unprocessed_pseudogene","ncbi_id":"8586","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71593454,"end":71594382,"strand":1,"description":"olfactory receptor family 7 subfamily E member 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:14709]"}, {"versioned_ensembl_gene_id":"ENSG00000283205.1","gene_symbol":"AL353572.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":87956214,"end":87956883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224366.1","gene_symbol":"AC243964.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44570304,"end":44570564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248903.1","gene_symbol":"AP000867.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71568680,"end":71568934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236823.1","gene_symbol":"AL035691.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159899186,"end":159902510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258065.1","gene_symbol":"AL122126.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28857384,"end":28858701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167895.14","gene_symbol":"TMC8","gene_name":"transmembrane channel like 8 [Source:HGNC Symbol;Acc:HGNC:20474]","synonyms":"EVER2,EVIN2","biotype":"protein_coding","ncbi_id":"147138","summary":"Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 8 predicted transmembrane domains and 3 leucine zipper motifs. [provided by RefSeq, Jul 2008]","start":78130770,"end":78142968,"strand":1,"description":"transmembrane channel like 8 [Source:HGNC Symbol;Acc:HGNC:20474]"}, {"versioned_ensembl_gene_id":"ENSG00000266998.1","gene_symbol":"AC111182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77373818,"end":77377236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267263.1","gene_symbol":"AC111170.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":77469068,"end":77471045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145715.14","gene_symbol":"RASA1","gene_name":"RAS p21 protein activator 1 [Source:HGNC Symbol;Acc:HGNC:9871]","synonyms":"p120,GAP,CM-AVM,RASA,p120RASGAP,p120GAP","biotype":"protein_coding","ncbi_id":"5921","summary":"The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012]","start":87267888,"end":87391931,"strand":1,"description":"RAS p21 protein activator 1 [Source:HGNC Symbol;Acc:HGNC:9871]"}, {"versioned_ensembl_gene_id":"ENSG00000153363.12","gene_symbol":"LINC00467","gene_name":"long intergenic non-protein coding RNA 467 [Source:HGNC Symbol;Acc:HGNC:28227]","synonyms":"MGC14801,C1orf97","biotype":"lincRNA","ncbi_id":"84791","summary":null,"start":211382803,"end":211435333,"strand":1,"description":"long intergenic non-protein coding RNA 467 [Source:HGNC Symbol;Acc:HGNC:28227]"}, {"versioned_ensembl_gene_id":"ENSG00000180884.9","gene_symbol":"ZNF792","gene_name":"zinc finger protein 792 [Source:HGNC Symbol;Acc:HGNC:24751]","synonyms":"FLJ38451","biotype":"protein_coding","ncbi_id":"126375","summary":null,"start":34956354,"end":34964049,"strand":-1,"description":"zinc finger protein 792 [Source:HGNC Symbol;Acc:HGNC:24751]"}, {"versioned_ensembl_gene_id":"ENSG00000178464.6","gene_symbol":"RPL10P16","gene_name":"ribosomal protein L10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36882]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284393","summary":null,"start":12643275,"end":12643919,"strand":-1,"description":"ribosomal protein L10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36882]"}, {"versioned_ensembl_gene_id":"ENSG00000168701.18","gene_symbol":"TMEM208","gene_name":"transmembrane protein 208 [Source:HGNC Symbol;Acc:HGNC:25015]","synonyms":"HSPC171","biotype":"protein_coding","ncbi_id":"29100","summary":"This gene encodes a highly conserved protein which is localized in the endoplasmic reticulum (ER). The protein is linked to autophagy and ER stress. Knockdown of this gene increased autophagy and triggered ER stress. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":67227103,"end":67229278,"strand":1,"description":"transmembrane protein 208 [Source:HGNC Symbol;Acc:HGNC:25015]"}, {"versioned_ensembl_gene_id":"ENSG00000230114.1","gene_symbol":"AL590432.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49257411,"end":49269285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215887.5","gene_symbol":"ZNF859P","gene_name":"zinc finger protein 859, pseudogene [Source:HGNC Symbol;Acc:HGNC:34507]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100507490","summary":null,"start":49841821,"end":49846400,"strand":1,"description":"zinc finger protein 859, pseudogene [Source:HGNC Symbol;Acc:HGNC:34507]"}, {"versioned_ensembl_gene_id":"ENSG00000256779.2","gene_symbol":"AP002383.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":95037482,"end":95039811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138813.9","gene_symbol":"C4orf17","gene_name":"chromosome 4 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:25274]","synonyms":"DKFZP434G072","biotype":"protein_coding","ncbi_id":"84103","summary":null,"start":99511004,"end":99542303,"strand":1,"description":"chromosome 4 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:25274]"}, {"versioned_ensembl_gene_id":"ENSG00000265908.1","gene_symbol":"AC024267.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28944796,"end":28945394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258729.2","gene_symbol":"AL355102.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96275046,"end":96276723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223551.1","gene_symbol":"TMSB4XP4","gene_name":"thymosin beta 4, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11886]","synonyms":"TMSL4","biotype":"processed_pseudogene","ncbi_id":"7118","summary":null,"start":128342153,"end":128342770,"strand":1,"description":"thymosin beta 4, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11886]"}, {"versioned_ensembl_gene_id":"ENSG00000260877.2","gene_symbol":"AP005233.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69371463,"end":69372512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224012.3","gene_symbol":"AC116917.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163709210,"end":163709514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249153.1","gene_symbol":"AC026414.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85848502,"end":85849199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250359.1","gene_symbol":"PTP4A1P4","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129564","summary":null,"start":86087526,"end":86087847,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41931]"}, {"versioned_ensembl_gene_id":"ENSG00000241965.2","gene_symbol":"RPS2P25","gene_name":"ribosomal protein S2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270913","summary":null,"start":85762559,"end":85763138,"strand":1,"description":"ribosomal protein S2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36410]"}, {"versioned_ensembl_gene_id":"ENSG00000250874.1","gene_symbol":"AC010595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85663232,"end":85664684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170476.15","gene_symbol":"MZB1","gene_name":"marginal zone B and B1 cell specific protein [Source:HGNC Symbol;Acc:HGNC:30125]","synonyms":"pERp1,PACAP,MGC29506,MEDA-7,HSPC190","biotype":"protein_coding","ncbi_id":"51237","summary":null,"start":139387480,"end":139390081,"strand":-1,"description":"marginal zone B and B1 cell specific protein [Source:HGNC Symbol;Acc:HGNC:30125]"}, {"versioned_ensembl_gene_id":"ENSG00000267168.1","gene_symbol":"AC005837.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76732978,"end":76738522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248667.1","gene_symbol":"AC010486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85420028,"end":85420451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275547.1","gene_symbol":"AC010632.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37024886,"end":37025254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231555.4","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31809921,"end":31812441,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000076944.15","gene_symbol":"STXBP2","gene_name":"syntaxin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11445]","synonyms":"UNC18B,Hunc18b","biotype":"protein_coding","ncbi_id":"6813","summary":"This gene encodes a member of the STXBP/unc-18/SEC1 family. The encoded protein is involved in intracellular trafficking, control of SNARE (soluble NSF attachment protein receptor) complex assembly, and the release of cytotoxic granules by natural killer cells. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2013]","start":7636881,"end":7647873,"strand":1,"description":"syntaxin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11445]"}, {"versioned_ensembl_gene_id":"ENSG00000204547.7","gene_symbol":"DEFB122","gene_name":"defensin beta 122 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18102]","synonyms":"DEFB122P,DEFB-22","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"245935","summary":null,"start":31421436,"end":31429180,"strand":-1,"description":"defensin beta 122 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18102]"}, {"versioned_ensembl_gene_id":"ENSG00000110395.6","gene_symbol":"CBL","gene_name":"Cbl proto-oncogene [Source:HGNC Symbol;Acc:HGNC:1541]","synonyms":"RNF55,CBL2,c-Cbl","biotype":"protein_coding","ncbi_id":"867","summary":"This gene is a proto-oncogene that encodes a RING finger E3 ubiquitin ligase. The encoded protein is one of the enzymes required for targeting substrates for degradation by the proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder. [provided by RefSeq, Jul 2016]","start":119206276,"end":119313926,"strand":1,"description":"Cbl proto-oncogene [Source:HGNC Symbol;Acc:HGNC:1541]"}, {"versioned_ensembl_gene_id":"ENSG00000260676.5","gene_symbol":"LINC01541","gene_name":"long intergenic non-protein coding RNA 1541 [Source:HGNC Symbol;Acc:HGNC:51309]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505776","summary":null,"start":71519962,"end":71578956,"strand":-1,"description":"long intergenic non-protein coding RNA 1541 [Source:HGNC Symbol;Acc:HGNC:51309]"}, {"versioned_ensembl_gene_id":"ENSG00000257057.2","gene_symbol":"C11orf97","gene_name":"chromosome 11 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:49544]","synonyms":"LINC01171","biotype":"protein_coding","ncbi_id":"643037","summary":null,"start":94512432,"end":94532123,"strand":1,"description":"chromosome 11 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:49544]"}, {"versioned_ensembl_gene_id":"ENSG00000270281.1","gene_symbol":"AC020910.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34779412,"end":34780021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144791.9","gene_symbol":"LIMD1","gene_name":"LIM domains containing 1 [Source:HGNC Symbol;Acc:HGNC:6612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8994","summary":null,"start":45555394,"end":45686338,"strand":1,"description":"LIM domains containing 1 [Source:HGNC Symbol;Acc:HGNC:6612]"}, {"versioned_ensembl_gene_id":"ENSG00000177350.6","gene_symbol":"RPL13AP3","gene_name":"ribosomal protein L13a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23539]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645683","summary":null,"start":55766177,"end":55767717,"strand":1,"description":"ribosomal protein L13a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23539]"}, {"versioned_ensembl_gene_id":"ENSG00000229000.1","gene_symbol":"SEPT7P8","gene_name":"septin 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418735","summary":null,"start":53772506,"end":53773280,"strand":-1,"description":"septin 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38044]"}, {"versioned_ensembl_gene_id":"ENSG00000134874.17","gene_symbol":"DZIP1","gene_name":"DAZ interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:20908]","synonyms":"KIAA0996,DZIP","biotype":"protein_coding","ncbi_id":"22873","summary":null,"start":95578202,"end":95644703,"strand":-1,"description":"DAZ interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:20908]"}, {"versioned_ensembl_gene_id":"ENSG00000281990.1","gene_symbol":"AC245369.4","gene_name":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106737110,"end":106737547,"strand":-1,"description":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]"}, {"versioned_ensembl_gene_id":"ENSG00000237589.1","gene_symbol":"HMGN1P32","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874465","summary":null,"start":53767971,"end":53768553,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39376]"}, {"versioned_ensembl_gene_id":"ENSG00000223506.2","gene_symbol":"SLC20A1P1","gene_name":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192127","summary":null,"start":106683395,"end":106684350,"strand":-1,"description":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]"}, {"versioned_ensembl_gene_id":"ENSG00000234475.5","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31797650,"end":31800132,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000154529.14","gene_symbol":"CNTNAP3B","gene_name":"contactin associated protein like 3B [Source:HGNC Symbol;Acc:HGNC:32035]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728577","summary":null,"start":41890314,"end":42129510,"strand":-1,"description":"contactin associated protein like 3B [Source:HGNC Symbol;Acc:HGNC:32035]"}, {"versioned_ensembl_gene_id":"ENSG00000276808.1","gene_symbol":"AC245128.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250013.1","gene_symbol":"AC093286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83875166,"end":83875821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269755.1","gene_symbol":"AC008758.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12433103,"end":12484816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272491.1","gene_symbol":"AL109659.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48227888,"end":48229561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278239.1","gene_symbol":"AC243967.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41833686,"end":41835950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249709.7","gene_symbol":"ZNF564","gene_name":"zinc finger protein 564 [Source:HGNC Symbol;Acc:HGNC:31106]","synonyms":"MGC26914","biotype":"protein_coding","ncbi_id":"163050","summary":null,"start":12525370,"end":12551542,"strand":-1,"description":"zinc finger protein 564 [Source:HGNC Symbol;Acc:HGNC:31106]"}, {"versioned_ensembl_gene_id":"ENSG00000234003.1","gene_symbol":"MTATP6P27","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52183]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075204","summary":null,"start":12506249,"end":12508030,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52183]"}, {"versioned_ensembl_gene_id":"ENSG00000168092.13","gene_symbol":"PAFAH1B2","gene_name":"platelet activating factor acetylhydrolase 1b catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:8575]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5049","summary":"Platelet-activating factor acetylhydrolase (PAFAH) inactivates platelet-activating factor (PAF) into acetate and LYSO-PAF. This gene encodes the beta subunit of PAFAH, the other subunits are alpha and gamma. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jan 2014]","start":117144267,"end":117176894,"strand":1,"description":"platelet activating factor acetylhydrolase 1b catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:8575]"}, {"versioned_ensembl_gene_id":"ENSG00000268744.1","gene_symbol":"AC008758.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12379189,"end":12401274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278318.4","gene_symbol":"ZNF229","gene_name":"zinc finger protein 229 [Source:HGNC Symbol;Acc:HGNC:13022]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7772","summary":null,"start":44417519,"end":44448578,"strand":-1,"description":"zinc finger protein 229 [Source:HGNC Symbol;Acc:HGNC:13022]"}, {"versioned_ensembl_gene_id":"ENSG00000261801.5","gene_symbol":"LOXL1-AS1","gene_name":"LOXL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44169]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287616","summary":null,"start":73908071,"end":73928248,"strand":-1,"description":"LOXL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44169]"}, {"versioned_ensembl_gene_id":"ENSG00000223568.1","gene_symbol":"RPL3P11","gene_name":"ribosomal protein L3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35521]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131893","summary":null,"start":14040716,"end":14041861,"strand":-1,"description":"ribosomal protein L3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35521]"}, {"versioned_ensembl_gene_id":"ENSG00000254678.1","gene_symbol":"AP005018.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117143891,"end":117144191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188033.9","gene_symbol":"ZNF490","gene_name":"zinc finger protein 490 [Source:HGNC Symbol;Acc:HGNC:23705]","synonyms":"KIAA1198","biotype":"protein_coding","ncbi_id":"57474","summary":null,"start":12577961,"end":12640098,"strand":-1,"description":"zinc finger protein 490 [Source:HGNC Symbol;Acc:HGNC:23705]"}, {"versioned_ensembl_gene_id":"ENSG00000261430.1","gene_symbol":"AL031600.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1467673,"end":1472684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175931.12","gene_symbol":"UBE2O","gene_name":"ubiquitin conjugating enzyme E2 O [Source:HGNC Symbol;Acc:HGNC:29554]","synonyms":"E2-230K","biotype":"protein_coding","ncbi_id":"63893","summary":null,"start":76389451,"end":76453206,"strand":-1,"description":"ubiquitin conjugating enzyme E2 O [Source:HGNC Symbol;Acc:HGNC:29554]"}, {"versioned_ensembl_gene_id":"ENSG00000231361.1","gene_symbol":"RPS29P23","gene_name":"ribosomal protein S29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271588","summary":null,"start":12373609,"end":12373731,"strand":1,"description":"ribosomal protein S29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35779]"}, {"versioned_ensembl_gene_id":"ENSG00000244468.1","gene_symbol":"AC093001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149284782,"end":149333653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107147.12","gene_symbol":"KCNT1","gene_name":"potassium sodium-activated channel subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:18865]","synonyms":"Slo2.2,SLACK,KIAA1422,KCa4.1","biotype":"protein_coding","ncbi_id":"57582","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":135702185,"end":135795508,"strand":1,"description":"potassium sodium-activated channel subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:18865]"}, {"versioned_ensembl_gene_id":"ENSG00000244345.1","gene_symbol":"AC104435.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72504806,"end":72550552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101280.7","gene_symbol":"ANGPT4","gene_name":"angiopoietin 4 [Source:HGNC Symbol;Acc:HGNC:487]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51378","summary":"Angiopoietins are proteins with important roles in vascular development and angiogenesis. All angiopoietins bind with similar affinity to an endothelial cell-specific tyrosine-protein kinase receptor. The mechanism by which they contribute to angiogenesis is thought to involve regulation of endothelial cell interactions with supporting perivascular cells. The protein encoded by this gene functions as an agonist and is an angiopoietin. [provided by RefSeq, Jul 2008]","start":869899,"end":916317,"strand":-1,"description":"angiopoietin 4 [Source:HGNC Symbol;Acc:HGNC:487]"}, {"versioned_ensembl_gene_id":"ENSG00000225137.1","gene_symbol":"DYNC1I2P1","gene_name":"dynein cytoplasmic 1 intermediate chain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728532","summary":null,"start":50264978,"end":50266815,"strand":1,"description":"dynein cytoplasmic 1 intermediate chain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45012]"}, {"versioned_ensembl_gene_id":"ENSG00000211972.2","gene_symbol":"IGHV3-66","gene_name":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28412","summary":null,"start":106675017,"end":106675544,"strand":-1,"description":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]"}, {"versioned_ensembl_gene_id":"ENSG00000086548.8","gene_symbol":"CEACAM6","gene_name":"carcinoembryonic antigen related cell adhesion molecule 6 [Source:HGNC Symbol;Acc:HGNC:1818]","synonyms":"NCA,CD66c","biotype":"protein_coding","ncbi_id":"4680","summary":"This gene encodes a protein that belongs to the carcinoembryonic antigen (CEA) family whose members are glycosyl phosphatidyl inositol (GPI) anchored cell surface glycoproteins. Members of this family play a role in cell adhesion and are widely used as tumor markers in serum immunoassay determinations of carcinoma. This gene affects the sensitivity of tumor cells to adenovirus infection. The protein encoded by this gene acts as a receptor for adherent-invasive E. coli adhesion to the surface of ileal epithelial cells in patients with Crohn's disease. This gene is clustered with genes and pseudogenes of the cell adhesion molecules subgroup of the CEA family on chromosome 19. [provided by RefSeq, Apr 2014]","start":41750977,"end":41772208,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 6 [Source:HGNC Symbol;Acc:HGNC:1818]"}, {"versioned_ensembl_gene_id":"ENSG00000279561.2","gene_symbol":"AL845472.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41269916,"end":41273997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158710.14","gene_symbol":"TAGLN2","gene_name":"transgelin 2 [Source:HGNC Symbol;Acc:HGNC:11554]","synonyms":"KIAA0120,HA1756","biotype":"protein_coding","ncbi_id":"8407","summary":"The protein encoded by this gene is similar to the protein transgelin, which is one of the earliest markers of differentiated smooth muscle. The specific function of this protein has not yet been determined, although it is thought to be a tumor suppressor. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":159918107,"end":159925732,"strand":-1,"description":"transgelin 2 [Source:HGNC Symbol;Acc:HGNC:11554]"}, {"versioned_ensembl_gene_id":"ENSG00000196290.14","gene_symbol":"NIF3L1","gene_name":"NGG1 interacting factor 3 like 1 [Source:HGNC Symbol;Acc:HGNC:13390]","synonyms":"ALS2CR1,MDS015,CALS-7","biotype":"protein_coding","ncbi_id":"60491","summary":null,"start":200889327,"end":200903930,"strand":1,"description":"NGG1 interacting factor 3 like 1 [Source:HGNC Symbol;Acc:HGNC:13390]"}, {"versioned_ensembl_gene_id":"ENSG00000100302.6","gene_symbol":"RASD2","gene_name":"RASD family member 2 [Source:HGNC Symbol;Acc:HGNC:18229]","synonyms":"TEM2,Rhes,MGC:4834","biotype":"protein_coding","ncbi_id":"23551","summary":"This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients. [provided by RefSeq, Jan 2016]","start":35540868,"end":35554001,"strand":1,"description":"RASD family member 2 [Source:HGNC Symbol;Acc:HGNC:18229]"}, {"versioned_ensembl_gene_id":"ENSG00000273044.1","gene_symbol":"AL022334.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35526932,"end":35527415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233388.2","gene_symbol":"AL022334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35501861,"end":35503586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276807.1","gene_symbol":"AC022188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73730048,"end":73731711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229112.1","gene_symbol":"AL356583.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246528562,"end":246528841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167110.17","gene_symbol":"GOLGA2","gene_name":"golgin A2 [Source:HGNC Symbol;Acc:HGNC:4425]","synonyms":"golgin-95,GM130","biotype":"protein_coding","ncbi_id":"2801","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This encoded protein has been postulated to play roles in the stacking of Golgi cisternae and in vesicular transport. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of these variants has not been determined. [provided by RefSeq, Feb 2010]","start":128255829,"end":128275995,"strand":-1,"description":"golgin A2 [Source:HGNC Symbol;Acc:HGNC:4425]"}, {"versioned_ensembl_gene_id":"ENSG00000279355.1","gene_symbol":"AGPAT4-IT1","gene_name":"AGPAT4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:20988]","synonyms":"NCRNA00241,FLJ23112,C6orf59","biotype":"TEC","ncbi_id":"79992","summary":null,"start":161160105,"end":161161982,"strand":-1,"description":"AGPAT4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:20988]"}, {"versioned_ensembl_gene_id":"ENSG00000241130.1","gene_symbol":"AC012100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50798670,"end":50798951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232403.1","gene_symbol":"AC009501.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63108118,"end":63108429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277531.2","gene_symbol":"PNMA8C","gene_name":"paraneoplastic Ma antigen family member 8C [Source:HGNC Symbol;Acc:HGNC:53427]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46424697,"end":46428951,"strand":-1,"description":"paraneoplastic Ma antigen family member 8C [Source:HGNC Symbol;Acc:HGNC:53427]"}, {"versioned_ensembl_gene_id":"ENSG00000167880.7","gene_symbol":"EVPL","gene_name":"envoplakin [Source:HGNC Symbol;Acc:HGNC:3503]","synonyms":"EVPK","biotype":"protein_coding","ncbi_id":"2125","summary":"This gene encodes a member of the plakin family of proteins that forms a component of desmosomes and the epidermal cornified envelope. This gene is located in the tylosis oesophageal cancer locus on chromosome 17q25, and its deletion is associated with both familial and sporadic forms of oesophageal squamous cell carcinoma. Patients suffering from the autoimmune mucocutaneous disorder, paraneoplastic pemphigus, develop antibodies against the encoded protein. [provided by RefSeq, Jul 2016]","start":76004502,"end":76027452,"strand":-1,"description":"envoplakin [Source:HGNC Symbol;Acc:HGNC:3503]"}, {"versioned_ensembl_gene_id":"ENSG00000263045.1","gene_symbol":"AC090286.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18986148,"end":18986334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236451.2","gene_symbol":"AC067956.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220450679,"end":220704566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239498.1","gene_symbol":"AC019211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220105656,"end":220450778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136546.13","gene_symbol":"SCN7A","gene_name":"sodium voltage-gated channel alpha subunit 7 [Source:HGNC Symbol;Acc:HGNC:10594]","synonyms":"SCN6A,Nav2.2,Nav2.1,NaG","biotype":"protein_coding","ncbi_id":"6332","summary":"This gene encodes one of the many voltage-gated sodium channel proteins. For proper functioning of neurons and muscles during action potentials, voltage-gated sodium channels direct sodium ion diffusion for membrane depolarization. This sodium channel protein has some atypical characteristics; the similarity between the human and mouse proteins is lower compared to other orthologous sodium channel pairs. Also, the S4 segments, which sense voltage changes, have fewer positive charged residues that in other sodium channels; domain 4 has fewer arginine and lysine residues compared to other sodium channel proteins. Several alternatively spliced transcript variants exist, but the full-length natures of all of them remain unknown. [provided by RefSeq, Dec 2011]","start":166403573,"end":166494247,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 7 [Source:HGNC Symbol;Acc:HGNC:10594]"}, {"versioned_ensembl_gene_id":"ENSG00000283657.1","gene_symbol":"AC074101.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":166414489,"end":166414729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211951.2","gene_symbol":"IGHV2-26","gene_name":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28455","summary":null,"start":106301396,"end":106301862,"strand":-1,"description":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]"}, {"versioned_ensembl_gene_id":"ENSG00000279359.1","gene_symbol":"AL359195.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80249710,"end":80254121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181333.11","gene_symbol":"HEPHL1","gene_name":"hephaestin like 1 [Source:HGNC Symbol;Acc:HGNC:30477]","synonyms":"DKFZp686F22190","biotype":"protein_coding","ncbi_id":"341208","summary":null,"start":94021361,"end":94113751,"strand":1,"description":"hephaestin like 1 [Source:HGNC Symbol;Acc:HGNC:30477]"}, {"versioned_ensembl_gene_id":"ENSG00000151893.14","gene_symbol":"CACUL1","gene_name":"CDK2 associated cullin domain 1 [Source:HGNC Symbol;Acc:HGNC:23727]","synonyms":"MGC33215,FLJ40409,CAC1,C10orf46","biotype":"protein_coding","ncbi_id":"143384","summary":null,"start":118674167,"end":118755249,"strand":-1,"description":"CDK2 associated cullin domain 1 [Source:HGNC Symbol;Acc:HGNC:23727]"}, {"versioned_ensembl_gene_id":"ENSG00000234382.2","gene_symbol":"AL513174.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80233664,"end":80245367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224842.2","gene_symbol":"AL161908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126589594,"end":126613700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170837.2","gene_symbol":"GPR27","gene_name":"G protein-coupled receptor 27 [Source:HGNC Symbol;Acc:HGNC:4482]","synonyms":"SREB1","biotype":"protein_coding","ncbi_id":"2850","summary":"GPR27 is a member of the G protein-coupled receptors (GPCRs), a large family of receptors that have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli such as neurotransmitters, hormones, or light induces an intracellular signaling cascade mediated by heterotrimeric GTP-binding proteins, or G proteins.[supplied by OMIM, May 2010]","start":71754050,"end":71756496,"strand":1,"description":"G protein-coupled receptor 27 [Source:HGNC Symbol;Acc:HGNC:4482]"}, {"versioned_ensembl_gene_id":"ENSG00000247867.2","gene_symbol":"AP001922.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75758455,"end":75768647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152582.13","gene_symbol":"SPEF2","gene_name":"sperm flagellar 2 [Source:HGNC Symbol;Acc:HGNC:26293]","synonyms":"KPL2,FLJ23577,CT122","biotype":"protein_coding","ncbi_id":"79925","summary":null,"start":35617844,"end":35814611,"strand":1,"description":"sperm flagellar 2 [Source:HGNC Symbol;Acc:HGNC:26293]"}, {"versioned_ensembl_gene_id":"ENSG00000253248.5","gene_symbol":"AC079098.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136047021,"end":136166122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149636.15","gene_symbol":"DSN1","gene_name":"DSN1 homolog, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16165]","synonyms":"C20orf172,MIS13,KNL3,hKNL-3,dJ469A13.2","biotype":"protein_coding","ncbi_id":"79980","summary":"This gene encodes a kinetochore protein that functions as part of the minichromosome instability-12 centromere complex. The encoded protein is required for proper kinetochore assembly and progression through the cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009]","start":36751791,"end":36773818,"strand":-1,"description":"DSN1 homolog, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16165]"}, {"versioned_ensembl_gene_id":"ENSG00000272444.1","gene_symbol":"AL118558.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101952416,"end":101953063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267254.5","gene_symbol":"ZNF790-AS1","gene_name":"ZNF790 antisense RNA 1 [Source:NCBI gene;Acc:284408]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"284408","summary":null,"start":36797518,"end":36828115,"strand":1,"description":"ZNF790 antisense RNA 1 [Source:NCBI gene;Acc:284408]"}, {"versioned_ensembl_gene_id":"ENSG00000254150.1","gene_symbol":"AC087664.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59557528,"end":59557855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205057.4","gene_symbol":"CLLU1OS","gene_name":"chronic lymphocytic leukemia up-regulated 1 opposite strand [Source:HGNC Symbol;Acc:HGNC:24070]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574016","summary":null,"start":92420094,"end":92428148,"strand":-1,"description":"chronic lymphocytic leukemia up-regulated 1 opposite strand [Source:HGNC Symbol;Acc:HGNC:24070]"}, {"versioned_ensembl_gene_id":"ENSG00000143125.5","gene_symbol":"PROK1","gene_name":"prokineticin 1 [Source:HGNC Symbol;Acc:HGNC:18454]","synonyms":"PRK1,PK1,EGVEGF","biotype":"protein_coding","ncbi_id":"84432","summary":"The protein encoded by this gene induces proliferation, migration, and fenestration (the formation of membrane discontinuities) in capillary endothelial cells derived from endocrine glands. It has little or no effect on a variety of other endothelial and non-endothelial cell types. Its expression is restricted to the steroidogenic glands (ovary, testis, adrenal, and placenta), is induced by hypoxia, and often complementary to the expression of vascular endothelial growth factor (VEGF), suggesting that these molecules function in a coordinated manner. [provided by RefSeq, Sep 2011]","start":110451200,"end":110457354,"strand":1,"description":"prokineticin 1 [Source:HGNC Symbol;Acc:HGNC:18454]"}, {"versioned_ensembl_gene_id":"ENSG00000138600.9","gene_symbol":"SPPL2A","gene_name":"signal peptide peptidase like 2A [Source:HGNC Symbol;Acc:HGNC:30227]","synonyms":"PSL2,IMP3","biotype":"protein_coding","ncbi_id":"84888","summary":"This gene encodes a member of the GXGD family of aspartic proteases, which are transmembrane proteins with two conserved catalytic motifs localized within the membrane-spanning regions, as well as a member of the signal peptide peptidase-like protease (SPPL) family. This protein is expressed in all major adult human tissues and localizes to late endosomal compartments and lysosomal membranes. A pseudogene of this gene also lies on chromosome 15. [provided by RefSeq, Feb 2012]","start":50702266,"end":50765808,"strand":-1,"description":"signal peptide peptidase like 2A [Source:HGNC Symbol;Acc:HGNC:30227]"}, {"versioned_ensembl_gene_id":"ENSG00000271201.1","gene_symbol":"AC247036.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106206603,"end":106208571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171806.11","gene_symbol":"METTL18","gene_name":"methyltransferase like 18 [Source:HGNC Symbol;Acc:HGNC:28793]","synonyms":"MGC9084,HPM1,C1orf156,AsTP2","biotype":"protein_coding","ncbi_id":"92342","summary":null,"start":169792529,"end":169794966,"strand":-1,"description":"methyltransferase like 18 [Source:HGNC Symbol;Acc:HGNC:28793]"}, {"versioned_ensembl_gene_id":"ENSG00000271795.1","gene_symbol":"AC011337.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151509453,"end":151512769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124089.4","gene_symbol":"MC3R","gene_name":"melanocortin 3 receptor [Source:HGNC Symbol;Acc:HGNC:6931]","synonyms":"MC3","biotype":"protein_coding","ncbi_id":"4159","summary":"This gene encodes a G-protein-coupled receptor for melanocyte-stimulating hormone and adrenocorticotropic hormone that is expressed in tissues other than the adrenal cortex and melanocytes. This gene maps to the same region as the locus for benign neonatal epilepsy. Mice deficient for this gene have increased fat mass despite decreased food intake, suggesting a role for this gene product in the regulation of energy homeostasis. Mutations in this gene are associated with a susceptibility to obesity in humans. [provided by RefSeq, Jul 2008]","start":56248732,"end":56249815,"strand":1,"description":"melanocortin 3 receptor [Source:HGNC Symbol;Acc:HGNC:6931]"}, {"versioned_ensembl_gene_id":"ENSG00000152380.9","gene_symbol":"FAM151B","gene_name":"family with sequence similarity 151 member B [Source:HGNC Symbol;Acc:HGNC:33716]","synonyms":"UNQ9217","biotype":"protein_coding","ncbi_id":"167555","summary":null,"start":80487969,"end":80542563,"strand":1,"description":"family with sequence similarity 151 member B [Source:HGNC Symbol;Acc:HGNC:33716]"}, {"versioned_ensembl_gene_id":"ENSG00000174677.4","gene_symbol":"VN1R6P","gene_name":"vomeronasal 1 receptor 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:13712]","synonyms":"ZVNR2,ZVNH2,VNR19I2","biotype":"unitary_pseudogene","ncbi_id":"653753","summary":null,"start":53315137,"end":53316043,"strand":1,"description":"vomeronasal 1 receptor 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:13712]"}, {"versioned_ensembl_gene_id":"ENSG00000269118.1","gene_symbol":"FAM90A28P","gene_name":"family with sequence similarity 90 member A28, pseudogene [Source:HGNC Symbol;Acc:HGNC:43747]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100128254","summary":null,"start":53299051,"end":53308644,"strand":-1,"description":"family with sequence similarity 90 member A28, pseudogene [Source:HGNC Symbol;Acc:HGNC:43747]"}, {"versioned_ensembl_gene_id":"ENSG00000132475.10","gene_symbol":"H3F3B","gene_name":"H3 histone family member 3B [Source:HGNC Symbol;Acc:HGNC:4765]","synonyms":"H3.3B","biotype":"protein_coding","ncbi_id":"3021","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene contains introns and its mRNA is polyadenylated, unlike most histone genes. The protein encoded by this gene is a replication-independent histone that is a member of the histone H3 family. Pseudogenes of this gene have been identified on the X chromosome, and on chromosomes 5, 13 and 17. [provided by RefSeq, Oct 2015]","start":75776434,"end":75785893,"strand":-1,"description":"H3 histone family member 3B [Source:HGNC Symbol;Acc:HGNC:4765]"}, {"versioned_ensembl_gene_id":"ENSG00000054803.3","gene_symbol":"CBLN4","gene_name":"cerebellin 4 precursor [Source:HGNC Symbol;Acc:HGNC:16231]","synonyms":"dJ885A10.1,CBLNL1","biotype":"protein_coding","ncbi_id":"140689","summary":"This gene encodes a member of a family of small secreted proteins containing C1Q domains. Members of this family are involved in regulation of neurexin signalling during synapse development. The mouse homolog of the protein encoded by this gene competes with netrin to bind to the deleted in colorectal cancer receptor. [provided by RefSeq, Aug 2012]","start":55997440,"end":56005472,"strand":-1,"description":"cerebellin 4 precursor [Source:HGNC Symbol;Acc:HGNC:16231]"}, {"versioned_ensembl_gene_id":"ENSG00000282639.1","gene_symbol":"AC247036.4","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106088122,"end":106088573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253387.1","gene_symbol":"IGHVIII-5-1","gene_name":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]","synonyms":"IGHV(III)-5-1","biotype":"IG_V_pseudogene","ncbi_id":"28354","summary":null,"start":106039666,"end":106039764,"strand":-1,"description":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]"}, {"versioned_ensembl_gene_id":"ENSG00000279036.1","gene_symbol":"AC015656.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49494223,"end":49497800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257458.1","gene_symbol":"AC069437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98931682,"end":98976656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118137.9","gene_symbol":"APOA1","gene_name":"apolipoprotein A1 [Source:HGNC Symbol;Acc:HGNC:600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"335","summary":"This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein. [provided by RefSeq, Dec 2015]","start":116835751,"end":116837950,"strand":-1,"description":"apolipoprotein A1 [Source:HGNC Symbol;Acc:HGNC:600]"}, {"versioned_ensembl_gene_id":"ENSG00000236341.1","gene_symbol":"AL161740.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56963886,"end":56996757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112276.13","gene_symbol":"BVES","gene_name":"blood vessel epicardial substance [Source:HGNC Symbol;Acc:HGNC:1152]","synonyms":"POPDC1,POP1,HBVES","biotype":"protein_coding","ncbi_id":"11149","summary":"This gene encodes a member of the POP family of proteins containing three putative transmembrane domains. This gene is expressed in cardiac and skeletal muscle and may play an important role in development of these tissues. The mouse ortholog may be involved in the regeneration of adult skeletal muscle and may act as a cell adhesion molecule in coronary vasculogenesis. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":105096822,"end":105137174,"strand":-1,"description":"blood vessel epicardial substance [Source:HGNC Symbol;Acc:HGNC:1152]"}, {"versioned_ensembl_gene_id":"ENSG00000284629.1","gene_symbol":"AC097662.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227387683,"end":227387949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226759.7","gene_symbol":"DAB1-AS1","gene_name":"DAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49443]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926890","summary":null,"start":57860532,"end":57880905,"strand":1,"description":"DAB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49443]"}, {"versioned_ensembl_gene_id":"ENSG00000206516.10","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457053,"end":29464201,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000122359.17","gene_symbol":"ANXA11","gene_name":"annexin A11 [Source:HGNC Symbol;Acc:HGNC:535]","synonyms":"ANX11","biotype":"protein_coding","ncbi_id":"311","summary":"This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]","start":80150889,"end":80205572,"strand":-1,"description":"annexin A11 [Source:HGNC Symbol;Acc:HGNC:535]"}, {"versioned_ensembl_gene_id":"ENSG00000275637.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54906192,"end":54910107,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000225884.2","gene_symbol":"AC098872.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":191793425,"end":191820250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174307.6","gene_symbol":"PHLDA3","gene_name":"pleckstrin homology like domain family A member 3 [Source:HGNC Symbol;Acc:HGNC:8934]","synonyms":"TIH1","biotype":"protein_coding","ncbi_id":"23612","summary":null,"start":201464383,"end":201469237,"strand":-1,"description":"pleckstrin homology like domain family A member 3 [Source:HGNC Symbol;Acc:HGNC:8934]"}, {"versioned_ensembl_gene_id":"ENSG00000168243.10","gene_symbol":"GNG4","gene_name":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2786","summary":null,"start":235547687,"end":235650754,"strand":-1,"description":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]"}, {"versioned_ensembl_gene_id":"ENSG00000179889.18","gene_symbol":"PDXDC1","gene_name":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]","synonyms":"KIAA0251,KIAA0251","biotype":"protein_coding","ncbi_id":"23042","summary":null,"start":14974591,"end":15139339,"strand":1,"description":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]"}, {"versioned_ensembl_gene_id":"ENSG00000235700.1","gene_symbol":"CYCSP52","gene_name":"cytochrome c, somatic pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:24393]","synonyms":"HC6,HCP2","biotype":"processed_pseudogene","ncbi_id":"360155","summary":null,"start":157128362,"end":157128671,"strand":1,"description":"cytochrome c, somatic pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:24393]"}, {"versioned_ensembl_gene_id":"ENSG00000253838.1","gene_symbol":"AC007991.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39914229,"end":39915721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242683.1","gene_symbol":"RPL12P21","gene_name":"ribosomal protein L12 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36845]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270921","summary":null,"start":139035148,"end":139035987,"strand":-1,"description":"ribosomal protein L12 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36845]"}, {"versioned_ensembl_gene_id":"ENSG00000109265.13","gene_symbol":"KIAA1211","gene_name":"KIAA1211 [Source:HGNC Symbol;Acc:HGNC:29219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57482","summary":null,"start":56049073,"end":56328625,"strand":1,"description":"KIAA1211 [Source:HGNC Symbol;Acc:HGNC:29219]"}, {"versioned_ensembl_gene_id":"ENSG00000230773.6","gene_symbol":"AC092650.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47941696,"end":48240983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223973.2","gene_symbol":"AC068491.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":111383752,"end":111384992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233599.8","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30208315,"end":30217805,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000249087.6","gene_symbol":"ZNF436-AS1","gene_name":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]","synonyms":"FLJ90508,C1orf213","biotype":"antisense_RNA","ncbi_id":"148898","summary":null,"start":23368997,"end":23371839,"strand":1,"description":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]"}, {"versioned_ensembl_gene_id":"ENSG00000273312.2","gene_symbol":"AL121749.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35604485,"end":35608153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273880.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54716322,"end":54720285,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000186815.12","gene_symbol":"TPCN1","gene_name":"two pore segment channel 1 [Source:HGNC Symbol;Acc:HGNC:18182]","synonyms":"TPC1,KIAA1169,FLJ20612","biotype":"protein_coding","ncbi_id":"53373","summary":"Voltage-gated Ca(2+) and Na+ channels have 4 homologous domains, each containing 6 transmembrane segments, S1 to S6. TPCN1 is similar to these channels, but it has only 2 domains containing S1 to S6 (Ishibashi et al., 2000 [PubMed 10753632]).[supplied by OMIM, Mar 2008]","start":113221050,"end":113298585,"strand":1,"description":"two pore segment channel 1 [Source:HGNC Symbol;Acc:HGNC:18182]"}, {"versioned_ensembl_gene_id":"ENSG00000213558.3","gene_symbol":"HMGN2P32","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39403]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874473","summary":null,"start":107458038,"end":107458306,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39403]"}, {"versioned_ensembl_gene_id":"ENSG00000172269.18","gene_symbol":"DPAGT1","gene_name":"dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:2995]","synonyms":"CDG-Ij,ALG7,GPT,DPAGT2,DPAGT,DGPT,D11S366","biotype":"protein_coding","ncbi_id":"1798","summary":"The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme. [provided by RefSeq, Jul 2008]","start":119096503,"end":119108331,"strand":-1,"description":"dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:2995]"}, {"versioned_ensembl_gene_id":"ENSG00000185271.7","gene_symbol":"KLHL33","gene_name":"kelch like family member 33 [Source:HGNC Symbol;Acc:HGNC:31952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123103","summary":null,"start":20425870,"end":20435811,"strand":-1,"description":"kelch like family member 33 [Source:HGNC Symbol;Acc:HGNC:31952]"}, {"versioned_ensembl_gene_id":"ENSG00000034693.14","gene_symbol":"PEX3","gene_name":"peroxisomal biogenesis factor 3 [Source:HGNC Symbol;Acc:HGNC:8858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8504","summary":"The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]","start":143450807,"end":143490010,"strand":1,"description":"peroxisomal biogenesis factor 3 [Source:HGNC Symbol;Acc:HGNC:8858]"}, {"versioned_ensembl_gene_id":"ENSG00000268606.5","gene_symbol":"MAGEA2","gene_name":"MAGE family member A2 [Source:HGNC Symbol;Acc:HGNC:6800]","synonyms":"MAGEA2A,MAGE2,CT1.2","biotype":"protein_coding","ncbi_id":"4101","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. Alternatively spliced transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":152749863,"end":152753884,"strand":-1,"description":"MAGE family member A2 [Source:HGNC Symbol;Acc:HGNC:6800]"}, {"versioned_ensembl_gene_id":"ENSG00000259140.2","gene_symbol":"AL049839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94674877,"end":94675829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235198.1","gene_symbol":"AC005871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117562084,"end":117572457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181513.14","gene_symbol":"ACBD4","gene_name":"acyl-CoA binding domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23337]","synonyms":"FLJ13322","biotype":"protein_coding","ncbi_id":"79777","summary":"This gene encodes a member of the acyl-coenzyme A binding domain containing protein family. All family members contain the conserved acyl-Coenzyme A binding domain, which binds acyl-CoA thiol esters. They are thought to play roles in acyl-CoA dependent lipid metabolism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":45132600,"end":45144181,"strand":1,"description":"acyl-CoA binding domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23337]"}, {"versioned_ensembl_gene_id":"ENSG00000225370.1","gene_symbol":"AC243962.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54671231,"end":54672591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250302.1","gene_symbol":"LINC01618","gene_name":"long intergenic non-protein coding RNA 1618 [Source:HGNC Symbol;Acc:HGNC:27195]","synonyms":"LOC152578","biotype":"lincRNA","ncbi_id":"152578","summary":null,"start":52789994,"end":52815464,"strand":1,"description":"long intergenic non-protein coding RNA 1618 [Source:HGNC Symbol;Acc:HGNC:27195]"}, {"versioned_ensembl_gene_id":"ENSG00000248423.1","gene_symbol":"AC100850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15688914,"end":15689562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254042.1","gene_symbol":"AC011365.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168706567,"end":168720884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073350.13","gene_symbol":"LLGL2","gene_name":"LLGL2, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6629]","synonyms":"Hugl-2,HGL","biotype":"protein_coding","ncbi_id":"3993","summary":"The lethal (2) giant larvae protein of Drosophila plays a role in asymmetric cell division, epithelial cell polarity, and cell migration. This human gene encodes a protein similar to lethal (2) giant larvae of Drosophila. In fly, the protein's ability to localize cell fate determinants is regulated by the atypical protein kinase C (aPKC). In human, this protein interacts with aPKC-containing complexes and is cortically localized in mitotic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":75525080,"end":75575208,"strand":1,"description":"LLGL2, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6629]"}, {"versioned_ensembl_gene_id":"ENSG00000181609.5","gene_symbol":"OR52D1","gene_name":"olfactory receptor family 52 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15212]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5488685,"end":5489749,"strand":1,"description":"olfactory receptor family 52 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15212]"}, {"versioned_ensembl_gene_id":"ENSG00000276409.4","gene_symbol":"CCL14","gene_name":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]","synonyms":"NCC-2,MCIF,HCC-3,HCC-1,CKb1,SCYL2,SCYA14","biotype":"protein_coding","ncbi_id":"6358","summary":"This gene, chemokine (C-C motif) ligand 14, is one of several CC cytokine genes clustered on 17q11.2. The CC cytokines are secreted proteins characterized by two adjacent cysteines. The cytokine encoded by this gene induces changes in intracellular calcium concentration and enzyme release in monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Read-through transcripts are also expressed that include exons from the upstream cytokine gene, chemokine (C-C motif) ligand 15, and are represented as GeneID: 348249. [provided by RefSeq, Dec 2009]","start":35983291,"end":35987004,"strand":-1,"description":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]"}, {"versioned_ensembl_gene_id":"ENSG00000175520.8","gene_symbol":"UBQLN3","gene_name":"ubiquilin 3 [Source:HGNC Symbol;Acc:HGNC:12510]","synonyms":"TUP-1","biotype":"protein_coding","ncbi_id":"50613","summary":"This gene encodes a ubiquitin-like protein (ubiquilin) that shares a high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain an N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically associate with both proteasomes and ubiquitin ligases, and are thus thought to functionally link the ubiquitination machinery to the proteasome to affect in vivo protein degradation. This gene is specifically expressed in the testis. It has been suggested that this gene may regulate cell-cycle progression during spermatogenesis, however, it has been shown that the ortholgous mouse gene is dispensable for embryonic development and spermatogenesis. [provided by RefSeq, Nov 2016]","start":5507300,"end":5509985,"strand":-1,"description":"ubiquilin 3 [Source:HGNC Symbol;Acc:HGNC:12510]"}, {"versioned_ensembl_gene_id":"ENSG00000167359.8","gene_symbol":"OR51I1","gene_name":"olfactory receptor family 51 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390063","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5440570,"end":5441514,"strand":-1,"description":"olfactory receptor family 51 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15200]"}, {"versioned_ensembl_gene_id":"ENSG00000279012.2","gene_symbol":"OR51B2","gene_name":"olfactory receptor family 51 subfamily B member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14703]","synonyms":"OR51B1P","biotype":"polymorphic_pseudogene","ncbi_id":"79345","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":5323359,"end":5324297,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14703]"}, {"versioned_ensembl_gene_id":"ENSG00000278492.1","gene_symbol":"AC006213.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43978376,"end":43978663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008226.19","gene_symbol":"DLEC1","gene_name":"deleted in lung and esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:2899]","synonyms":"DLC1,CFAP81","biotype":"protein_coding","ncbi_id":"9940","summary":"The cytogenetic location of this gene is 3p21.3, and it is located in a region that is commonly deleted in a variety of malignancies. Down-regulation of this gene has been observed in several human cancers including lung, esophageal, renal tumors, and head and neck squamous cell carcinoma. In some cases, reduced expression of this gene in tumor cells is a result of aberrant promoter methylation. Several alternatively spliced transcripts have been observed that contain disrupted coding regions and likely encode nonfunctional proteins.[provided by RefSeq, Mar 2016]","start":38039205,"end":38124025,"strand":1,"description":"deleted in lung and esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:2899]"}, {"versioned_ensembl_gene_id":"ENSG00000168930.13","gene_symbol":"TRIM49","gene_name":"tripartite motif containing 49 [Source:HGNC Symbol;Acc:HGNC:13431]","synonyms":"TRIM49A,RNF18","biotype":"protein_coding","ncbi_id":"57093","summary":"The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This gene has been found to be preferentially expressed in testis. Related pseudogenes and gene duplicates have also been identified on chromosome 11. [provided by RefSeq, Aug 2010]","start":89797655,"end":89808575,"strand":-1,"description":"tripartite motif containing 49 [Source:HGNC Symbol;Acc:HGNC:13431]"}, {"versioned_ensembl_gene_id":"ENSG00000255162.1","gene_symbol":"AP004833.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89785945,"end":89787838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243716.10","gene_symbol":"NPIPB5","gene_name":"nuclear pore complex interacting protein family member B5 [Source:HGNC Symbol;Acc:HGNC:37233]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132247","summary":null,"start":22479121,"end":22536521,"strand":1,"description":"nuclear pore complex interacting protein family member B5 [Source:HGNC Symbol;Acc:HGNC:37233]"}, {"versioned_ensembl_gene_id":"ENSG00000275485.1","gene_symbol":"AL512652.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":20768876,"end":20769375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233835.1","gene_symbol":"AL132875.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79871873,"end":79874610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254411.1","gene_symbol":"AP002512.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56495760,"end":56496412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232034.1","gene_symbol":"AC092168.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":100822661,"end":100847220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273510.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769838,"end":54784324,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000278177.1","gene_symbol":"AL354811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93226612,"end":93227317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256995.6","gene_symbol":"AC084816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22699859,"end":23174125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256923.1","gene_symbol":"AC084819.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22742582,"end":22743091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170356.9","gene_symbol":"OR2A20P","gene_name":"olfactory receptor family 2 subfamily A member 20 pseudogene [Source:NCBI gene;Acc:401428]","synonyms":"OR2A20","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401428","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144250045,"end":144256244,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 20 pseudogene [Source:NCBI gene;Acc:401428]"}, {"versioned_ensembl_gene_id":"ENSG00000164399.4","gene_symbol":"IL3","gene_name":"interleukin 3 [Source:HGNC Symbol;Acc:HGNC:6011]","synonyms":"MULTI-CSF,MGC79399,MGC79398,MCGF,IL-3","biotype":"protein_coding","ncbi_id":"3562","summary":"The protein encoded by this gene is a potent growth promoting cytokine. This cytokine is capable of supporting the proliferation of a broad range of hematopoietic cell types. It is involved in a variety of cell activities such as cell growth, differentiation and apoptosis. This cytokine has been shown to also possess neurotrophic activity, and it may be associated with neurologic disorders. [provided by RefSeq, Jul 2008]","start":132060529,"end":132063204,"strand":1,"description":"interleukin 3 [Source:HGNC Symbol;Acc:HGNC:6011]"}, {"versioned_ensembl_gene_id":"ENSG00000257809.1","gene_symbol":"AC034102.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56150796,"end":56158220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226046.1","gene_symbol":"AP1S2P1","gene_name":"adaptor related protein complex 1 sigma 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480305","summary":null,"start":97437518,"end":97437896,"strand":1,"description":"adaptor related protein complex 1 sigma 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50752]"}, {"versioned_ensembl_gene_id":"ENSG00000131480.8","gene_symbol":"AOC2","gene_name":"amine oxidase, copper containing 2 [Source:HGNC Symbol;Acc:HGNC:549]","synonyms":"RAO,DAO2","biotype":"protein_coding","ncbi_id":"314","summary":"Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":42844600,"end":42850707,"strand":1,"description":"amine oxidase, copper containing 2 [Source:HGNC Symbol;Acc:HGNC:549]"}, {"versioned_ensembl_gene_id":"ENSG00000253424.1","gene_symbol":"AC025437.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158256137,"end":158258436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277556.1","gene_symbol":"OR13C5","gene_name":"olfactory receptor family 13 subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:15100]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138799","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104598457,"end":104599413,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:15100]"}, {"versioned_ensembl_gene_id":"ENSG00000277087.1","gene_symbol":"AL121890.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5045761,"end":5046276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259146.3","gene_symbol":"AC005476.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71292729,"end":71321814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275106.1","gene_symbol":"AC025594.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":128952527,"end":128953316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277490.1","gene_symbol":"BX664608.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66879454,"end":66879940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153485.5","gene_symbol":"TMEM251","gene_name":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]","synonyms":"DKFZP564F1123,C14orf109","biotype":"protein_coding","ncbi_id":"26175","summary":null,"start":93184951,"end":93187089,"strand":1,"description":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]"}, {"versioned_ensembl_gene_id":"ENSG00000228237.5","gene_symbol":"EFCAB14-AS1","gene_name":"EFCAB14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44108]","synonyms":"KIAA0494-AS1","biotype":"antisense_RNA","ncbi_id":"100130197","summary":null,"start":46674036,"end":46692098,"strand":1,"description":"EFCAB14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44108]"}, {"versioned_ensembl_gene_id":"ENSG00000229115.1","gene_symbol":"AL390774.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123759220,"end":123759775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230536.1","gene_symbol":"AL360268.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128090969,"end":128094457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234771.3","gene_symbol":"SLC25A25-AS1","gene_name":"SLC25A25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27844]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289019","summary":null,"start":128108581,"end":128118693,"strand":-1,"description":"SLC25A25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27844]"}, {"versioned_ensembl_gene_id":"ENSG00000265298.1","gene_symbol":"AC132812.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64750420,"end":64751311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130165.10","gene_symbol":"ELOF1","gene_name":"elongation factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:28691]","synonyms":"MGC4549,ELF1","biotype":"protein_coding","ncbi_id":"84337","summary":null,"start":11551147,"end":11559236,"strand":-1,"description":"elongation factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:28691]"}, {"versioned_ensembl_gene_id":"ENSG00000227706.3","gene_symbol":"AL713998.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67887646,"end":67889339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256551.1","gene_symbol":"LINC02369","gene_name":"long intergenic non-protein coding RNA 2369 [Source:HGNC Symbol;Acc:HGNC:53292]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996679","summary":null,"start":128086985,"end":128118132,"strand":-1,"description":"long intergenic non-protein coding RNA 2369 [Source:HGNC Symbol;Acc:HGNC:53292]"}, {"versioned_ensembl_gene_id":"ENSG00000186152.6","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000139613.11","gene_symbol":"SMARCC2","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2 [Source:HGNC Symbol;Acc:HGNC:11105]","synonyms":"BAF170,Rsc8,CRACC2","biotype":"protein_coding","ncbi_id":"6601","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and contains a predicted leucine zipper motif typical of many transcription factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56162983,"end":56189567,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2 [Source:HGNC Symbol;Acc:HGNC:11105]"}, {"versioned_ensembl_gene_id":"ENSG00000231128.5","gene_symbol":"AL137856.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113812379,"end":113829171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235448.1","gene_symbol":"LURAP1L-AS1","gene_name":"LURAP1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49761]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929467","summary":null,"start":12700100,"end":12814345,"strand":-1,"description":"LURAP1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49761]"}, {"versioned_ensembl_gene_id":"ENSG00000134852.14","gene_symbol":"CLOCK","gene_name":"clock circadian regulator [Source:HGNC Symbol;Acc:HGNC:2082]","synonyms":"KIAA0334,KAT13D,bHLHe8","biotype":"protein_coding","ncbi_id":"9575","summary":"The protein encoded by this gene plays a central role in the regulation of circadian rhythms. The protein encodes a transcription factor of the basic helix-loop-helix (bHLH) family and contains DNA binding histone acetyltransferase activity. The encoded protein forms a heterodimer with ARNTL (BMAL1) that binds E-box enhancer elements upstream of Period (PER1, PER2, PER3) and Cryptochrome (CRY1, CRY2) genes and activates transcription of these genes. PER and CRY proteins heterodimerize and repress their own transcription by interacting in a feedback loop with CLOCK/ARNTL complexes. Polymorphisms in this gene may be associated with behavioral changes in certain populations and with obesity and metabolic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":55427903,"end":55547138,"strand":-1,"description":"clock circadian regulator [Source:HGNC Symbol;Acc:HGNC:2082]"}, {"versioned_ensembl_gene_id":"ENSG00000140463.13","gene_symbol":"BBS4","gene_name":"Bardet-Biedl syndrome 4 [Source:HGNC Symbol;Acc:HGNC:969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"585","summary":"This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein \"BBSome\" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":72686179,"end":72738476,"strand":1,"description":"Bardet-Biedl syndrome 4 [Source:HGNC Symbol;Acc:HGNC:969]"}, {"versioned_ensembl_gene_id":"ENSG00000237541.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32741342,"end":32747215,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000259881.1","gene_symbol":"AC092384.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88881038,"end":88887136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232748.3","gene_symbol":"AC135050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31056460,"end":31062803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169242.11","gene_symbol":"EFNA1","gene_name":"ephrin A1 [Source:HGNC Symbol;Acc:HGNC:3221]","synonyms":"TNFAIP4,LERK1,EPLG1,ECKLG","biotype":"protein_coding","ncbi_id":"1942","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNA class ephrin which binds to the EPHA2, EPHA4, EPHA5, EPHA6, and EPHA7 receptors. Two transcript variants that encode different isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":155127460,"end":155134857,"strand":1,"description":"ephrin A1 [Source:HGNC Symbol;Acc:HGNC:3221]"}, {"versioned_ensembl_gene_id":"ENSG00000127418.14","gene_symbol":"FGFRL1","gene_name":"fibroblast growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:3693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53834","summary":"The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. A marked difference between this gene product and the other family members is its lack of a cytoplasmic tyrosine kinase domain. The result is a transmembrane receptor that could interact with other family members and potentially inhibit signaling. Multiple alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":1009936,"end":1026897,"strand":1,"description":"fibroblast growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:3693]"}, {"versioned_ensembl_gene_id":"ENSG00000280500.1","gene_symbol":"ELMO2P1","gene_name":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729894","summary":null,"start":23086215,"end":23124800,"strand":1,"description":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]"}, {"versioned_ensembl_gene_id":"ENSG00000226721.2","gene_symbol":"EEF1DP2","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33523]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442429","summary":null,"start":92836826,"end":92837668,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33523]"}, {"versioned_ensembl_gene_id":"ENSG00000259912.1","gene_symbol":"AC023813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48620319,"end":48622033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259565.2","gene_symbol":"KRT8P23","gene_name":"keratin 8 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390610","summary":null,"start":76979245,"end":76980451,"strand":-1,"description":"keratin 8 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33375]"}, {"versioned_ensembl_gene_id":"ENSG00000186008.7","gene_symbol":"RPS4XP21","gene_name":"ribosomal protein S4X pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36228]","synonyms":"RPS4P21","biotype":"processed_pseudogene","ncbi_id":"126235","summary":null,"start":34092561,"end":34093310,"strand":-1,"description":"ribosomal protein S4X pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36228]"}, {"versioned_ensembl_gene_id":"ENSG00000261267.1","gene_symbol":"AC026470.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48559661,"end":48587403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243364.7","gene_symbol":"EFNA4","gene_name":"ephrin A4 [Source:HGNC Symbol;Acc:HGNC:3224]","synonyms":"LERK4,EPLG4","biotype":"protein_coding","ncbi_id":"1945","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNA class ephrin. Three transcript variants that encode distinct proteins have been identified. [provided by RefSeq, Jul 2008]","start":155063731,"end":155069553,"strand":1,"description":"ephrin A4 [Source:HGNC Symbol;Acc:HGNC:3224]"}, {"versioned_ensembl_gene_id":"ENSG00000259153.1","gene_symbol":"AC004816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70810205,"end":70815403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165168.7","gene_symbol":"CYBB","gene_name":"cytochrome b-245 beta chain [Source:HGNC Symbol;Acc:HGNC:2578]","synonyms":"NOX2,GP91-PHOX,CGD","biotype":"protein_coding","ncbi_id":"1536","summary":"Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain. It has been proposed as a primary component of the microbicidal oxidase system of phagocytes. CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte NADPH oxidase; neutrophils are able to phagocytize bacteria but cannot kill them in the phagocytic vacuoles. The cause of the killing defect is an inability to increase the cell's respiration and consequent failure to deliver activated oxygen into the phagocytic vacuole. [provided by RefSeq, Jul 2008]","start":37780011,"end":37813461,"strand":1,"description":"cytochrome b-245 beta chain [Source:HGNC Symbol;Acc:HGNC:2578]"}, {"versioned_ensembl_gene_id":"ENSG00000170290.3","gene_symbol":"SLN","gene_name":"sarcolipin [Source:HGNC Symbol;Acc:HGNC:11089]","synonyms":"MGC125855,MGC125854,MGC12301","biotype":"protein_coding","ncbi_id":"6588","summary":"Sarcoplasmic reticulum Ca(2+)-ATPases are transmembrane proteins that catalyze the ATP-dependent transport of Ca(2+) from the cytosol into the lumen of the sarcoplasmic reticulum in muscle cells. This gene encodes a small proteolipid that regulates several sarcoplasmic reticulum Ca(2+)-ATPases. The transmembrane protein interacts with Ca(2+)-ATPases and reduces the accumulation of Ca(2+) in the sarcoplasmic reticulum without affecting the rate of ATP hydrolysis. [provided by RefSeq, Jul 2008]","start":107707378,"end":107719693,"strand":-1,"description":"sarcolipin [Source:HGNC Symbol;Acc:HGNC:11089]"}, {"versioned_ensembl_gene_id":"ENSG00000258532.1","gene_symbol":"LINC02305","gene_name":"long intergenic non-protein coding RNA 2305 [Source:HGNC Symbol;Acc:HGNC:53224]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724338","summary":null,"start":83906872,"end":83915050,"strand":-1,"description":"long intergenic non-protein coding RNA 2305 [Source:HGNC Symbol;Acc:HGNC:53224]"}, {"versioned_ensembl_gene_id":"ENSG00000223766.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"Em:AB014077.1,CAT56,Em:AB023052.2","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30601522,"end":30608359,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000188394.6","gene_symbol":"GPR21","gene_name":"G protein-coupled receptor 21 [Source:HGNC Symbol;Acc:HGNC:4476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2844","summary":"This gene encodes a member of the G-protein-coupled receptor 1 family. G-protein coupled receptors are membrane proteins which activate signaling cascades as a response to extracellular stress. The encoded protein activates a Gq signal transduction pathway which mobilizes calcium. [provided by RefSeq, Nov 2012]","start":123034527,"end":123035696,"strand":1,"description":"G protein-coupled receptor 21 [Source:HGNC Symbol;Acc:HGNC:4476]"}, {"versioned_ensembl_gene_id":"ENSG00000136404.15","gene_symbol":"TM6SF1","gene_name":"transmembrane 6 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53346","summary":null,"start":83107407,"end":83144854,"strand":1,"description":"transmembrane 6 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11860]"}, {"versioned_ensembl_gene_id":"ENSG00000237314.2","gene_symbol":"RPL12P39","gene_name":"ribosomal protein L12 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:35976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271410","summary":null,"start":64072158,"end":64072653,"strand":1,"description":"ribosomal protein L12 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:35976]"}, {"versioned_ensembl_gene_id":"ENSG00000173276.13","gene_symbol":"ZBTB21","gene_name":"zinc finger and BTB domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13083]","synonyms":"ZNF295,KIAA1227","biotype":"protein_coding","ncbi_id":"49854","summary":null,"start":41986831,"end":42010387,"strand":-1,"description":"zinc finger and BTB domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13083]"}, {"versioned_ensembl_gene_id":"ENSG00000234062.7","gene_symbol":"AL390879.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":136909395,"end":137021630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225078.2","gene_symbol":"AL365338.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123061845,"end":123063312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235778.1","gene_symbol":"AC130360.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7341826,"end":7342942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205424.1","gene_symbol":"AL592528.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45827961,"end":45836419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249446.2","gene_symbol":"TRAJ60","gene_name":"T-cell receptor alpha joining 60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12093]","synonyms":null,"biotype":"TR_J_pseudogene","ncbi_id":"28695","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22476306,"end":22476362,"strand":1,"description":"T-cell receptor alpha joining 60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12093]"}, {"versioned_ensembl_gene_id":"ENSG00000274959.1","gene_symbol":"SPDYE13P","gene_name":"speedy/RINGO cell cycle regulator family member E13, pseudogene [Source:HGNC Symbol;Acc:HGNC:51509]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105180390","summary":null,"start":75281267,"end":75287118,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E13, pseudogene [Source:HGNC Symbol;Acc:HGNC:51509]"}, {"versioned_ensembl_gene_id":"ENSG00000270137.1","gene_symbol":"AF230666.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":132826179,"end":132826903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278313.1","gene_symbol":"AC100827.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72604399,"end":72605008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165355.7","gene_symbol":"FBXO33","gene_name":"F-box protein 33 [Source:HGNC Symbol;Acc:HGNC:19833]","synonyms":"Fbx33","biotype":"protein_coding","ncbi_id":"254170","summary":"This locus represents an member of the F-box gene family. The encoded protein contains an F-box motif and a domain that might form a structure similar to a leucine-rich repeat found in placental RNAse inhibitor. This locus may be associated with copy number variation of UGT2B17 (GeneID 7367), which has been associated with susceptibility to osteoporosis.[provided by RefSeq, Sep 2010]","start":39397669,"end":39432500,"strand":-1,"description":"F-box protein 33 [Source:HGNC Symbol;Acc:HGNC:19833]"}, {"versioned_ensembl_gene_id":"ENSG00000227329.2","gene_symbol":"AL139396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53164391,"end":53164557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103319.11","gene_symbol":"EEF2K","gene_name":"eukaryotic elongation factor 2 kinase [Source:HGNC Symbol;Acc:HGNC:24615]","synonyms":"eEF-2K","biotype":"protein_coding","ncbi_id":"29904","summary":"This gene encodes a highly conserved protein kinase in the calmodulin-mediated signaling pathway that links activation of cell surface receptors to cell division. This kinase is involved in the regulation of protein synthesis. It phosphorylates eukaryotic elongation factor 2 (EEF2) and thus inhibits the EEF2 function. The activity of this kinase is increased in many cancers and may be a valid target for anti-cancer treatment. [provided by RefSeq, Jul 2008]","start":22206282,"end":22288732,"strand":1,"description":"eukaryotic elongation factor 2 kinase [Source:HGNC Symbol;Acc:HGNC:24615]"}, {"versioned_ensembl_gene_id":"ENSG00000211829.9","gene_symbol":"TRDC","gene_name":"T-cell receptor delta constant [Source:HGNC Symbol;Acc:HGNC:12253]","synonyms":null,"biotype":"TR_C_gene","ncbi_id":"28526","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22462932,"end":22465787,"strand":1,"description":"T-cell receptor delta constant [Source:HGNC Symbol;Acc:HGNC:12253]"}, {"versioned_ensembl_gene_id":"ENSG00000211827.1","gene_symbol":"TRDJ2","gene_name":"T-cell receptor delta joining 2 [Source:HGNC Symbol;Acc:HGNC:12258]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28521","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22456689,"end":22456742,"strand":1,"description":"T-cell receptor delta joining 2 [Source:HGNC Symbol;Acc:HGNC:12258]"}, {"versioned_ensembl_gene_id":"ENSG00000259042.2","gene_symbol":"AC244502.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22417836,"end":22418657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237444.1","gene_symbol":"AP001342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25031005,"end":25031529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237235.2","gene_symbol":"TRDD2","gene_name":"T-cell receptor delta diversity 2 [Source:HGNC Symbol;Acc:HGNC:12255]","synonyms":null,"biotype":"TR_D_gene","ncbi_id":"28524","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22439007,"end":22439015,"strand":1,"description":"T-cell receptor delta diversity 2 [Source:HGNC Symbol;Acc:HGNC:12255]"}, {"versioned_ensembl_gene_id":"ENSG00000184916.8","gene_symbol":"JAG2","gene_name":"jagged 2 [Source:HGNC Symbol;Acc:HGNC:6189]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3714","summary":"The Notch signaling pathway is an intercellular signaling mechanism that is essential for proper embryonic development. Members of the Notch gene family encode transmembrane receptors that are critical for various cell fate decisions. The protein encoded by this gene is one of several ligands that activate Notch and related receptors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":105140981,"end":105168824,"strand":-1,"description":"jagged 2 [Source:HGNC Symbol;Acc:HGNC:6189]"}, {"versioned_ensembl_gene_id":"ENSG00000251111.2","gene_symbol":"FCF1P8","gene_name":"FCF1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422531","summary":null,"start":55351812,"end":55352408,"strand":-1,"description":"FCF1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44620]"}, {"versioned_ensembl_gene_id":"ENSG00000117419.14","gene_symbol":"ERI3","gene_name":"ERI1 exoribonuclease family member 3 [Source:HGNC Symbol;Acc:HGNC:17276]","synonyms":"PRNPIP,PINT1,FLJ22943","biotype":"protein_coding","ncbi_id":"79033","summary":null,"start":44221070,"end":44355260,"strand":-1,"description":"ERI1 exoribonuclease family member 3 [Source:HGNC Symbol;Acc:HGNC:17276]"}, {"versioned_ensembl_gene_id":"ENSG00000271398.1","gene_symbol":"AL353622.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28247144,"end":28247568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279433.1","gene_symbol":"AC018529.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77108284,"end":77110537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197712.11","gene_symbol":"FAM114A1","gene_name":"family with sequence similarity 114 member A1 [Source:HGNC Symbol;Acc:HGNC:25087]","synonyms":"Noxp20","biotype":"protein_coding","ncbi_id":"92689","summary":"The protein encoded by this gene belongs to the FAM114 family and may play a role in neuronal cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":38867677,"end":38945739,"strand":1,"description":"family with sequence similarity 114 member A1 [Source:HGNC Symbol;Acc:HGNC:25087]"}, {"versioned_ensembl_gene_id":"ENSG00000274447.1","gene_symbol":"AC005790.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5294247,"end":5294696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198373.12","gene_symbol":"WWP2","gene_name":"WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16804]","synonyms":"AIP2","biotype":"protein_coding","ncbi_id":"11060","summary":"This gene encodes a member of the Nedd4 family of E3 ligases, which play an important role in protein ubiquitination. The encoded protein contains four WW domains and may play a role in multiple processes including chondrogenesis and the regulation of oncogenic signaling pathways via interactions with Smad proteins and the tumor suppressor PTEN. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 10. [provided by RefSeq, Jul 2012]","start":69762306,"end":69941741,"strand":1,"description":"WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16804]"}, {"versioned_ensembl_gene_id":"ENSG00000238035.8","gene_symbol":"AC138035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181306502,"end":181324685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279064.1","gene_symbol":"FP236315.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5707004,"end":5709456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183283.15","gene_symbol":"DAZAP2","gene_name":"DAZ associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2684]","synonyms":"KIAA0058","biotype":"protein_coding","ncbi_id":"9802","summary":"This gene encodes a proline-rich protein which interacts with the deleted in azoospermia (DAZ) and the deleted in azoospermia-like gene through the DAZ-like repeats. This protein also interacts with the transforming growth factor-beta signaling molecule SARA (Smad anchor for receptor activation), eukaryotic initiation factor 4G, and an E3 ubiquitinase that regulates its stability in splicing factor containing nuclear speckles. The encoded protein may function in various biological and pathological processes including spermatogenesis, cell signaling and transcription regulation, formation of stress granules during translation arrest, RNA splicing, and pathogenesis of multiple myeloma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":51238292,"end":51271362,"strand":1,"description":"DAZ associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2684]"}, {"versioned_ensembl_gene_id":"ENSG00000213073.4","gene_symbol":"AL353625.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":160093082,"end":160096212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183484.11","gene_symbol":"GPR132","gene_name":"G protein-coupled receptor 132 [Source:HGNC Symbol;Acc:HGNC:17482]","synonyms":"G2A","biotype":"protein_coding","ncbi_id":"29933","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor (GPCR) superfamily. The receptors are seven-pass transmembrane proteins that respond to extracellular cues and activate intracellular signal transduction pathways. This protein was reported to be a receptor for lysophosphatidylcholine action, but PubMedID: 15653487 retracts this finding and instead suggests this protein to be an effector of lysophosphatidylcholine action. This protein may have proton-sensing activity and may be a receptor for oxidized free fatty acids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":105049389,"end":105065445,"strand":-1,"description":"G protein-coupled receptor 132 [Source:HGNC Symbol;Acc:HGNC:17482]"}, {"versioned_ensembl_gene_id":"ENSG00000132581.9","gene_symbol":"SDF2","gene_name":"stromal cell derived factor 2 [Source:HGNC Symbol;Acc:HGNC:10675]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6388","summary":"The protein encoded by this gene is believed to be a secretory protein. It has regions of similarity to hydrophilic segments of yeast mannosyltransferases. Its expression is ubiquitous and the gene appears to be relatively conserved among mammals. Alternate splicing results in both coding and non-coding variants. A pseudogene of this gene is located on chromosome 15. [provided by RefSeq, Dec 2011]","start":28648356,"end":28662189,"strand":-1,"description":"stromal cell derived factor 2 [Source:HGNC Symbol;Acc:HGNC:10675]"}, {"versioned_ensembl_gene_id":"ENSG00000220744.1","gene_symbol":"RPL5P18","gene_name":"ribosomal protein L5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389428","summary":null,"start":127362513,"end":127363403,"strand":1,"description":"ribosomal protein L5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36640]"}, {"versioned_ensembl_gene_id":"ENSG00000230798.5","gene_symbol":"FOXD3-AS1","gene_name":"FOXD3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40241]","synonyms":"pasFOXD3","biotype":"antisense_RNA","ncbi_id":"100996301","summary":null,"start":63320884,"end":63324441,"strand":-1,"description":"FOXD3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40241]"}, {"versioned_ensembl_gene_id":"ENSG00000236467.8","gene_symbol":"KCNMA1-AS1","gene_name":"KCNMA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51213]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929328","summary":null,"start":76888044,"end":76980624,"strand":1,"description":"KCNMA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51213]"}, {"versioned_ensembl_gene_id":"ENSG00000215482.3","gene_symbol":"CALM2P3","gene_name":"calmodulin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"807","summary":null,"start":41170700,"end":41171148,"strand":-1,"description":"calmodulin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1448]"}, {"versioned_ensembl_gene_id":"ENSG00000137142.4","gene_symbol":"IGFBPL1","gene_name":"insulin like growth factor binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:20081]","synonyms":"bA113O24.1","biotype":"protein_coding","ncbi_id":"347252","summary":null,"start":38408994,"end":38424447,"strand":-1,"description":"insulin like growth factor binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:20081]"}, {"versioned_ensembl_gene_id":"ENSG00000266549.1","gene_symbol":"AC023575.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26952201,"end":26952558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184515.10","gene_symbol":"BEX5","gene_name":"brain expressed X-linked 5 [Source:HGNC Symbol;Acc:HGNC:27990]","synonyms":"NGFRAP1L1","biotype":"protein_coding","ncbi_id":"340542","summary":null,"start":102153708,"end":102156057,"strand":-1,"description":"brain expressed X-linked 5 [Source:HGNC Symbol;Acc:HGNC:27990]"}, {"versioned_ensembl_gene_id":"ENSG00000231683.6","gene_symbol":"AL033397.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53561289,"end":53617171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254063.2","gene_symbol":"DUXAP2","gene_name":"double homeobox A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32181]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"503631","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":101366417,"end":101367005,"strand":-1,"description":"double homeobox A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32181]"}, {"versioned_ensembl_gene_id":"ENSG00000251488.1","gene_symbol":"AC115622.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132836772,"end":132981677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143954.12","gene_symbol":"REG3G","gene_name":"regenerating family member 3 gamma [Source:HGNC Symbol;Acc:HGNC:29595]","synonyms":"UNQ429,PAP1B,LPPM429","biotype":"protein_coding","ncbi_id":"130120","summary":"This gene encodes a member of the regenerating islet-derived genes (REG)3 protein family. These proteins are secreted, C-type lectins with a carbohydrate recognition domain and N-terminal signal peptide. The protein encoded by this gene is an antimicrobial lectin with activity against Gram-positive bacteria. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Nov 2014]","start":79025686,"end":79028505,"strand":1,"description":"regenerating family member 3 gamma [Source:HGNC Symbol;Acc:HGNC:29595]"}, {"versioned_ensembl_gene_id":"ENSG00000255336.1","gene_symbol":"AP003181.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":105246880,"end":105247060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253942.1","gene_symbol":"AP001330.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101223941,"end":101224573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279936.1","gene_symbol":"AC008806.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37401404,"end":37403846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129946.10","gene_symbol":"SHC2","gene_name":"SHC adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:29869]","synonyms":"SLI,SHCB,SCK","biotype":"protein_coding","ncbi_id":"25759","summary":null,"start":416583,"end":460996,"strand":-1,"description":"SHC adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:29869]"}, {"versioned_ensembl_gene_id":"ENSG00000232790.2","gene_symbol":"LINC01162","gene_name":"long intergenic non-protein coding RNA 1162 [Source:HGNC Symbol;Acc:HGNC:49528]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355138","summary":null,"start":20835431,"end":21023148,"strand":1,"description":"long intergenic non-protein coding RNA 1162 [Source:HGNC Symbol;Acc:HGNC:49528]"}, {"versioned_ensembl_gene_id":"ENSG00000234839.1","gene_symbol":"RPS26P30","gene_name":"ribosomal protein S26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35574]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271111","summary":null,"start":20843627,"end":20843961,"strand":1,"description":"ribosomal protein S26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35574]"}, {"versioned_ensembl_gene_id":"ENSG00000227411.1","gene_symbol":"BAATP1","gene_name":"bile acid-CoA: amino acid N-acyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34504]","synonyms":"ACNATP","biotype":"unitary_pseudogene","ncbi_id":"347275","summary":null,"start":101334084,"end":101339347,"strand":-1,"description":"bile acid-CoA: amino acid N-acyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34504]"}, {"versioned_ensembl_gene_id":"ENSG00000260517.3","gene_symbol":"AC009093.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29139661,"end":29216706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130368.5","gene_symbol":"MAS1","gene_name":"MAS1 proto-oncogene, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:6899]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4142","summary":"This gene encodes a class I seven-transmembrane G-protein-coupled receptor. The encoded protein is a receptor for angiotensin-(1-7) and preferentially couples to the Gq protein, activating the phospholipase C signaling pathway. The encoded protein may play a role in multiple processes including hypotension, smooth muscle relaxation and cardioprotection by mediating the effects of angiotensin-(1-7). [provided by RefSeq, May 2012]","start":159906690,"end":159916530,"strand":1,"description":"MAS1 proto-oncogene, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:6899]"}, {"versioned_ensembl_gene_id":"ENSG00000083457.11","gene_symbol":"ITGAE","gene_name":"integrin subunit alpha E [Source:HGNC Symbol;Acc:HGNC:6147]","synonyms":"HUMINAE,CD103","biotype":"protein_coding","ncbi_id":"3682","summary":"Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This gene encodes an I-domain-containing alpha integrin that undergoes post-translational cleavage in the extracellular domain, yielding disulfide-linked heavy and light chains. In combination with the beta 7 integrin, this protein forms the E-cadherin binding integrin known as the human mucosal lymphocyte-1 antigen. This protein is preferentially expressed in human intestinal intraepithelial lymphocytes (IEL), and in addition to a role in adhesion, it may serve as an accessory molecule for IEL activation. [provided by RefSeq, Jul 2008]","start":3714628,"end":3801243,"strand":-1,"description":"integrin subunit alpha E [Source:HGNC Symbol;Acc:HGNC:6147]"}, {"versioned_ensembl_gene_id":"ENSG00000280257.1","gene_symbol":"AC007741.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":65790039,"end":65793533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113300.11","gene_symbol":"CNOT6","gene_name":"CCR4-NOT transcription complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14099]","synonyms":"KIAA1194,Ccr4a,CCR4","biotype":"protein_coding","ncbi_id":"57472","summary":"This gene encodes the catalytic component of the CCR4-NOT core transcriptional regulation complex. The encoded protein has a 3'-5' RNase activity and prefers polyadenylated substrates. The CCR4-NOT complex plays a role in many cellular processes, including miRNA-mediated repression, mRNA degradation, and transcriptional regulation. [provided by RefSeq, Dec 2014]","start":180494412,"end":180578405,"strand":1,"description":"CCR4-NOT transcription complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14099]"}, {"versioned_ensembl_gene_id":"ENSG00000255172.2","gene_symbol":"OR5AM1P","gene_name":"olfactory receptor family 5 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15254]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81226","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56619779,"end":56620810,"strand":-1,"description":"olfactory receptor family 5 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15254]"}, {"versioned_ensembl_gene_id":"ENSG00000249463.1","gene_symbol":"AC096711.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132027175,"end":132028434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108439.10","gene_symbol":"PNPO","gene_name":"pyridoxamine 5'-phosphate oxidase [Source:HGNC Symbol;Acc:HGNC:30260]","synonyms":"PDXPO","biotype":"protein_coding","ncbi_id":"55163","summary":"The enzyme encoded by this gene catalyzes the terminal, rate-limiting step in the synthesis of pyridoxal 5'-phosphate, also known as vitamin B6. Vitamin B6 is a required co-factor for enzymes involved in both homocysteine metabolism and synthesis of neurotransmitters such as catecholamine. Mutations in this gene result in pyridoxamine 5'-phosphate oxidase (PNPO) deficiency, a form of neonatal epileptic encephalopathy. [provided by RefSeq, Oct 2008]","start":47941506,"end":47949308,"strand":1,"description":"pyridoxamine 5'-phosphate oxidase [Source:HGNC Symbol;Acc:HGNC:30260]"}, {"versioned_ensembl_gene_id":"ENSG00000251598.1","gene_symbol":"AC096711.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132004810,"end":132124031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238265.1","gene_symbol":"LINC00317","gene_name":"long intergenic non-protein coding RNA 317 [Source:HGNC Symbol;Acc:HGNC:23126]","synonyms":"NCRNA00317,C21orf117,PRED89","biotype":"lincRNA","ncbi_id":"378828","summary":null,"start":21723293,"end":21737319,"strand":-1,"description":"long intergenic non-protein coding RNA 317 [Source:HGNC Symbol;Acc:HGNC:23126]"}, {"versioned_ensembl_gene_id":"ENSG00000237527.1","gene_symbol":"AF241725.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21655038,"end":21686329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283000.1","gene_symbol":"AL392046.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34969909,"end":34975578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135241.16","gene_symbol":"PNPLA8","gene_name":"patatin like phospholipase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28900]","synonyms":"iPLA2gamma,IPLA2G,IPLA2-2","biotype":"protein_coding","ncbi_id":"50640","summary":"This gene encodes a member of the patatin-like phospholipase domain containing protein family. Members of this family are phospholipases which catalyze the cleavage of fatty acids from membrane phospholipids. The product of this gene is a calcium-independent phospholipase. Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2015]","start":108470422,"end":108569666,"strand":-1,"description":"patatin like phospholipase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28900]"}, {"versioned_ensembl_gene_id":"ENSG00000204110.6","gene_symbol":"LINC02520","gene_name":"long intergenic non-protein coding RNA 2520 [Source:HGNC Symbol;Acc:HGNC:53511]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505530","summary":null,"start":37507348,"end":37535616,"strand":1,"description":"long intergenic non-protein coding RNA 2520 [Source:HGNC Symbol;Acc:HGNC:53511]"}, {"versioned_ensembl_gene_id":"ENSG00000225553.7","gene_symbol":"PHF1","gene_name":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]","synonyms":"MTF2L2,TDRD19C,PCL1","biotype":"protein_coding","ncbi_id":"5252","summary":"This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":33550562,"end":33556643,"strand":1,"description":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]"}, {"versioned_ensembl_gene_id":"ENSG00000231048.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"B144,LST-1,D6S49E","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31625572,"end":31628357,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000250844.2","gene_symbol":"USP17L18","gene_name":"ubiquitin specific peptidase 17-like family member 18 [Source:HGNC Symbol;Acc:HGNC:44446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287364","summary":null,"start":9248630,"end":9250581,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 18 [Source:HGNC Symbol;Acc:HGNC:44446]"}, {"versioned_ensembl_gene_id":"ENSG00000140022.9","gene_symbol":"STON2","gene_name":"stonin 2 [Source:HGNC Symbol;Acc:HGNC:30652]","synonyms":"STN2,STNB2","biotype":"protein_coding","ncbi_id":"85439","summary":"This gene encodes a protein which is a membrane protein involved in regulating endocytotic complexes. The protein product is described as one of the clathrin-associated sorting proteins, adaptor molecules which ensure specific proteins are internalized. The encoded protein has also been shown to participate in synaptic vesicle recycling through interaction with synaptotagmin 1 required for neurotransmission. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":81260656,"end":81436465,"strand":-1,"description":"stonin 2 [Source:HGNC Symbol;Acc:HGNC:30652]"}, {"versioned_ensembl_gene_id":"ENSG00000251010.1","gene_symbol":"AC097372.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146241806,"end":146243669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253114.2","gene_symbol":"AC090151.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54696398,"end":54697127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177455.12","gene_symbol":"CD19","gene_name":"CD19 molecule [Source:HGNC Symbol;Acc:HGNC:1633]","synonyms":null,"biotype":"protein_coding","ncbi_id":"930","summary":"This gene encodes a member of the immunoglobulin gene superfamily. Expression of this cell surface protein is restricted to B cell lymphocytes. This protein is a reliable marker for pre-B cells but its expression diminishes during terminal B cell differentiation in antibody secreting plasma cells. The protein has two N-terminal extracellular Ig-like domains separated by a non-Ig-like domain, a hydrophobic transmembrane domain, and a large C-terminal cytoplasmic domain. This protein forms a complex with several membrane proteins including complement receptor type 2 (CD21) and tetraspanin (CD81) and this complex reduces the threshold for antigen-initiated B cell activation. Activation of this B-cell antigen receptor complex activates the phosphatidylinositol 3-kinase signalling pathway and the subsequent release of intracellular stores of calcium ions. This protein is a target of chimeric antigen receptor (CAR) T-cells used in the treatment of lymphoblastic leukemia. Mutations in this gene are associated with the disease common variable immunodeficiency 3 (CVID3) which results in a failure of B-cell differentiation and impaired secretion of immunoglobulins. CVID3 is characterized by hypogammaglobulinemia, an inability to mount an antibody response to antigen, and recurrent bacterial infections. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2020]","start":28931939,"end":28939346,"strand":1,"description":"CD19 molecule [Source:HGNC Symbol;Acc:HGNC:1633]"}, {"versioned_ensembl_gene_id":"ENSG00000260442.5","gene_symbol":"ATP2A1-AS1","gene_name":"ATP2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51370]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289092","summary":null,"start":28878957,"end":28879920,"strand":-1,"description":"ATP2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51370]"}, {"versioned_ensembl_gene_id":"ENSG00000143799.12","gene_symbol":"PARP1","gene_name":"poly(ADP-ribose) polymerase 1 [Source:HGNC Symbol;Acc:HGNC:270]","synonyms":"PARP,ADPRT,PPOL","biotype":"protein_coding","ncbi_id":"142","summary":"This gene encodes a chromatin-associated enzyme, poly(ADP-ribosyl)transferase, which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation, proliferation, and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition, this enzyme may be the site of mutation in Fanconi anemia, and may participate in the pathophysiology of type I diabetes. [provided by RefSeq, Jul 2008]","start":226360691,"end":226408079,"strand":-1,"description":"poly(ADP-ribose) polymerase 1 [Source:HGNC Symbol;Acc:HGNC:270]"}, {"versioned_ensembl_gene_id":"ENSG00000103742.11","gene_symbol":"IGDCC4","gene_name":"immunoglobulin superfamily DCC subclass member 4 [Source:HGNC Symbol;Acc:HGNC:13770]","synonyms":"NOPE,LOC57722","biotype":"protein_coding","ncbi_id":"57722","summary":null,"start":65381464,"end":65423072,"strand":-1,"description":"immunoglobulin superfamily DCC subclass member 4 [Source:HGNC Symbol;Acc:HGNC:13770]"}, {"versioned_ensembl_gene_id":"ENSG00000100599.15","gene_symbol":"RIN3","gene_name":"Ras and Rab interactor 3 [Source:HGNC Symbol;Acc:HGNC:18751]","synonyms":"FLJ22439","biotype":"protein_coding","ncbi_id":"79890","summary":"Summary: This protein encoded by this gene is a member of the RIN family of Ras interaction-interference proteins, which are binding partners to the RAB5 small GTPases. The protein functions as a guanine nucleotide exchange for RAB5B and RAB31. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":92513774,"end":92688994,"strand":1,"description":"Ras and Rab interactor 3 [Source:HGNC Symbol;Acc:HGNC:18751]"}, {"versioned_ensembl_gene_id":"ENSG00000204687.4","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"MAS-L,dJ994E9.2,MRG","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486697,"end":29487956,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000229867.1","gene_symbol":"STEAP3-AS1","gene_name":"STEAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41053]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874111","summary":null,"start":119244422,"end":119249071,"strand":-1,"description":"STEAP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41053]"}, {"versioned_ensembl_gene_id":"ENSG00000275629.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"cl-5,nkat4b,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54849620,"end":54866390,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000249104.2","gene_symbol":"USP17L17","gene_name":"ubiquitin specific peptidase 17-like family member 17 [Source:HGNC Symbol;Acc:HGNC:44445]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287327","summary":null,"start":9243879,"end":9245830,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 17 [Source:HGNC Symbol;Acc:HGNC:44445]"}, {"versioned_ensembl_gene_id":"ENSG00000168765.16","gene_symbol":"GSTM4","gene_name":"glutathione S-transferase mu 4 [Source:HGNC Symbol;Acc:HGNC:4636]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2948","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. Multiple transcript variants, each encoding a distinct protein isoform, have been identified. [provided by RefSeq, Jul 2008]","start":109656081,"end":109674836,"strand":1,"description":"glutathione S-transferase mu 4 [Source:HGNC Symbol;Acc:HGNC:4636]"}, {"versioned_ensembl_gene_id":"ENSG00000178585.14","gene_symbol":"CTNNBIP1","gene_name":"catenin beta interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16913]","synonyms":"MGC15093,ICAT","biotype":"protein_coding","ncbi_id":"56998","summary":"The protein encoded by this gene binds CTNNB1 and prevents interaction between CTNNB1 and TCF family members. The encoded protein is a negative regulator of the Wnt signaling pathway. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":9848276,"end":9910336,"strand":-1,"description":"catenin beta interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16913]"}, {"versioned_ensembl_gene_id":"ENSG00000276631.1","gene_symbol":"AC007786.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29222542,"end":29223137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000026559.13","gene_symbol":"KCNG1","gene_name":"potassium voltage-gated channel modifier subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:6248]","synonyms":"KCNG,K13,Kv6.1,kH2","biotype":"protein_coding","ncbi_id":"3755","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This gene is abundantly expressed in skeletal muscle. Multiple alternatively spliced transcript variants have been found in normal and cancerous tissues. [provided by RefSeq, Jul 2008]","start":51003656,"end":51023129,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:6248]"}, {"versioned_ensembl_gene_id":"ENSG00000223569.6","gene_symbol":"USP17L15","gene_name":"ubiquitin specific peptidase 17-like family member 15 [Source:HGNC Symbol;Acc:HGNC:44443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288520","summary":null,"start":9234385,"end":9236334,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 15 [Source:HGNC Symbol;Acc:HGNC:44443]"}, {"versioned_ensembl_gene_id":"ENSG00000256763.1","gene_symbol":"LINC02467","gene_name":"long intergenic non-protein coding RNA 2467 [Source:HGNC Symbol;Acc:HGNC:53404]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984446","summary":null,"start":126168235,"end":126171666,"strand":1,"description":"long intergenic non-protein coding RNA 2467 [Source:HGNC Symbol;Acc:HGNC:53404]"}, {"versioned_ensembl_gene_id":"ENSG00000223356.1","gene_symbol":"AL590666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156712212,"end":156713174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234877.2","gene_symbol":"AC092660.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78597911,"end":78599406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166349.9","gene_symbol":"RAG1","gene_name":"recombination activating 1 [Source:HGNC Symbol;Acc:HGNC:9831]","synonyms":"RNF74,MGC43321","biotype":"protein_coding","ncbi_id":"5896","summary":"The protein encoded by this gene is involved in activation of immunoglobulin V-D-J recombination. The encoded protein is involved in recognition of the DNA substrate, but stable binding and cleavage activity also requires RAG2. Defects in this gene can be the cause of several diseases. [provided by RefSeq, Jul 2008]","start":36510709,"end":36593156,"strand":1,"description":"recombination activating 1 [Source:HGNC Symbol;Acc:HGNC:9831]"}, {"versioned_ensembl_gene_id":"ENSG00000270470.1","gene_symbol":"AC064872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78437850,"end":78438921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226898.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555714,"end":29560028,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000203668.2","gene_symbol":"CHML","gene_name":"CHM like, Rab escort protein 2 [Source:HGNC Symbol;Acc:HGNC:1941]","synonyms":"REP-2","biotype":"protein_coding","ncbi_id":"1122","summary":"The product of the CHML gene supports geranylgeranylation of most Rab proteins and may substitute for REP-1 in tissues other than retina. CHML is localized close to the gene for Usher syndrome type II. [provided by RefSeq, Jul 2008]","start":241628853,"end":241640254,"strand":-1,"description":"CHM like, Rab escort protein 2 [Source:HGNC Symbol;Acc:HGNC:1941]"}, {"versioned_ensembl_gene_id":"ENSG00000270765.5","gene_symbol":"GAS2L2","gene_name":"growth arrest specific 2 like 2 [Source:HGNC Symbol;Acc:HGNC:24846]","synonyms":"GAR17","biotype":"protein_coding","ncbi_id":"246176","summary":"The protein encoded by this gene appears to crosslink microtubules and microfilaments and may be part of the cytoskeleton. This gene is mainly expressed in skeletal muscle. [provided by RefSeq, Jul 2011]","start":35744511,"end":35752878,"strand":-1,"description":"growth arrest specific 2 like 2 [Source:HGNC Symbol;Acc:HGNC:24846]"}, {"versioned_ensembl_gene_id":"ENSG00000232399.3","gene_symbol":"USP17L13","gene_name":"ubiquitin specific peptidase 17-like family member 13 [Source:HGNC Symbol;Acc:HGNC:44441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287238","summary":null,"start":9224896,"end":9226847,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 13 [Source:HGNC Symbol;Acc:HGNC:44441]"}, {"versioned_ensembl_gene_id":"ENSG00000227551.1","gene_symbol":"USP17L12","gene_name":"ubiquitin specific peptidase 17-like family member 12 [Source:HGNC Symbol;Acc:HGNC:44440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287205","summary":null,"start":9220152,"end":9221744,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 12 [Source:HGNC Symbol;Acc:HGNC:44440]"}, {"versioned_ensembl_gene_id":"ENSG00000142227.10","gene_symbol":"EMP3","gene_name":"epithelial membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3335]","synonyms":"YMP","biotype":"protein_coding","ncbi_id":"2014","summary":"The protein encoded by this gene belongs to the PMP-22/EMP/MP20 family of proteins. The protein contains four transmembrane domains and two N-linked glycosylation sites. It is thought to be involved in cell proliferation, cell-cell interactions and function as a tumor suppressor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":48321509,"end":48330553,"strand":1,"description":"epithelial membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3335]"}, {"versioned_ensembl_gene_id":"ENSG00000214429.3","gene_symbol":"CYCSP6","gene_name":"cytochrome c, somatic pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24421]","synonyms":"HCP6","biotype":"processed_pseudogene","ncbi_id":"360159","summary":null,"start":78412793,"end":78413094,"strand":-1,"description":"cytochrome c, somatic pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:24421]"}, {"versioned_ensembl_gene_id":"ENSG00000148019.12","gene_symbol":"CEP78","gene_name":"centrosomal protein 78 [Source:HGNC Symbol;Acc:HGNC:25740]","synonyms":"FLJ12643,C9orf81","biotype":"protein_coding","ncbi_id":"84131","summary":"This gene encodes a centrosomal protein that is both required for the regulation of centrosome-related events during the cell cycle, and required for ciliogenesis. The encoded protein has an N-terminal leucine-rich repeat (LRR) domain with six consecutive LRR repeats, and a C-terminal coiled-coil domain. It interacts with the N-terminal catalytic domain of polo-like kinase 4 (PLK4) and colocalizes with PLK4 to the distal end of the centriole. Naturally occurring mutations in this gene cause defects in primary cilia that result in retinal degeneration and sensorineural hearing loss which are associated with cone-rod degeneration disease as well as Usher syndrome. Low expression of this gene is associated with poor prognosis of colorectal cancer patients. [provided by RefSeq, Mar 2017]","start":78236062,"end":78279690,"strand":1,"description":"centrosomal protein 78 [Source:HGNC Symbol;Acc:HGNC:25740]"}, {"versioned_ensembl_gene_id":"ENSG00000233136.2","gene_symbol":"USP17L11","gene_name":"ubiquitin specific peptidase 17-like family member 11 [Source:HGNC Symbol;Acc:HGNC:44439]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287178","summary":null,"start":9215405,"end":9217356,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 11 [Source:HGNC Symbol;Acc:HGNC:44439]"}, {"versioned_ensembl_gene_id":"ENSG00000232376.4","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"dJ570F3.6,APT,LYPLA2L","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33294377,"end":33295072,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000232653.8","gene_symbol":"GOLGA8N","gene_name":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643699","summary":null,"start":32593456,"end":32607310,"strand":1,"description":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]"}, {"versioned_ensembl_gene_id":"ENSG00000276724.1","gene_symbol":"AC123768.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32583612,"end":32584312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249416.2","gene_symbol":"AC107393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131768233,"end":131768578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250102.5","gene_symbol":"LINC02377","gene_name":"long intergenic non-protein coding RNA 2377 [Source:HGNC Symbol;Acc:HGNC:53300]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377424","summary":null,"start":131380013,"end":131541397,"strand":1,"description":"long intergenic non-protein coding RNA 2377 [Source:HGNC Symbol;Acc:HGNC:53300]"}, {"versioned_ensembl_gene_id":"ENSG00000225797.2","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464596,"end":29469806,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000223509.8","gene_symbol":"AC135983.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32519848,"end":32536926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272410.5","gene_symbol":"AC022384.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10249372,"end":10285796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271447.5","gene_symbol":"MMP28","gene_name":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]","synonyms":"EPILYSIN,MMP-28,MMP-25,MM28","biotype":"protein_coding","ncbi_id":"79148","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction and tissue remodeling, and disease processes, such as asthma and metastasis. This gene encodes a secreted enzyme that degrades casein. Its expression pattern suggests that it plays a role in tissue homeostasis and in wound repair. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":35756249,"end":35795707,"strand":-1,"description":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]"}, {"versioned_ensembl_gene_id":"ENSG00000088320.3","gene_symbol":"REM1","gene_name":"RRAD and GEM like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:15922]","synonyms":"REM,GES","biotype":"protein_coding","ncbi_id":"28954","summary":"The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells. [provided by RefSeq, Jul 2008]","start":31475293,"end":31484905,"strand":1,"description":"RRAD and GEM like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:15922]"}, {"versioned_ensembl_gene_id":"ENSG00000144061.12","gene_symbol":"NPHP1","gene_name":"nephrocystin 1 [Source:HGNC Symbol;Acc:HGNC:7905]","synonyms":"SLSN1,NPH1,JBTS4","biotype":"protein_coding","ncbi_id":"4867","summary":"This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":110122311,"end":110205066,"strand":-1,"description":"nephrocystin 1 [Source:HGNC Symbol;Acc:HGNC:7905]"}, {"versioned_ensembl_gene_id":"ENSG00000082898.16","gene_symbol":"XPO1","gene_name":"exportin 1 [Source:HGNC Symbol;Acc:HGNC:12825]","synonyms":"emb,CRM1","biotype":"protein_coding","ncbi_id":"7514","summary":"This cell-cycle-regulated gene encodes a protein that mediates leucine-rich nuclear export signal (NES)-dependent protein transport. The protein specifically inhibits the nuclear export of Rev and U snRNAs. It is involved in the control of several cellular processes by controlling the localization of cyclin B, MPAK, and MAPKAP kinase 2. This protein also regulates NFAT and AP-1. [provided by RefSeq, Jan 2015]","start":61477849,"end":61538626,"strand":-1,"description":"exportin 1 [Source:HGNC Symbol;Acc:HGNC:12825]"}, {"versioned_ensembl_gene_id":"ENSG00000229143.1","gene_symbol":"AC009480.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147810346,"end":147810777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278613.4","gene_symbol":"NAIP","gene_name":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]","synonyms":"NLRB1,BIRC1","biotype":"protein_coding","ncbi_id":"4671","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length; additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":69602550,"end":69659159,"strand":1,"description":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]"}, {"versioned_ensembl_gene_id":"ENSG00000175097.7","gene_symbol":"RAG2","gene_name":"recombination activating 2 [Source:HGNC Symbol;Acc:HGNC:9832]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5897","summary":"This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008]","start":36575574,"end":36598279,"strand":-1,"description":"recombination activating 2 [Source:HGNC Symbol;Acc:HGNC:9832]"}, {"versioned_ensembl_gene_id":"ENSG00000084710.13","gene_symbol":"EFR3B","gene_name":"EFR3 homolog B [Source:HGNC Symbol;Acc:HGNC:29155]","synonyms":"KIAA0953,FLJ37871","biotype":"protein_coding","ncbi_id":"22979","summary":null,"start":25042130,"end":25159137,"strand":1,"description":"EFR3 homolog B [Source:HGNC Symbol;Acc:HGNC:29155]"}, {"versioned_ensembl_gene_id":"ENSG00000180424.6","gene_symbol":"DEFB123","gene_name":"defensin beta 123 [Source:HGNC Symbol;Acc:HGNC:18103]","synonyms":"DEFB-23","biotype":"protein_coding","ncbi_id":"245936","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the host immunologic response to invading microorganisms. This antimicrobial protein is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20q11.1. Two transcript variants, one protein-coding and the other not, have been found for this gene. [provided by RefSeq, Nov 2014]","start":31440519,"end":31450257,"strand":1,"description":"defensin beta 123 [Source:HGNC Symbol;Acc:HGNC:18103]"}, {"versioned_ensembl_gene_id":"ENSG00000237440.8","gene_symbol":"ZNF737","gene_name":"zinc finger protein 737 [Source:HGNC Symbol;Acc:HGNC:32468]","synonyms":"ZNF102","biotype":"protein_coding","ncbi_id":"100129842","summary":null,"start":20535825,"end":20565809,"strand":-1,"description":"zinc finger protein 737 [Source:HGNC Symbol;Acc:HGNC:32468]"}, {"versioned_ensembl_gene_id":"ENSG00000103266.10","gene_symbol":"STUB1","gene_name":"STIP1 homology and U-box containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11427]","synonyms":"UBOX1,SDCCAG7,NY-CO-7,HSPABP2,CHIP","biotype":"protein_coding","ncbi_id":"10273","summary":"This gene encodes a protein containing tetratricopeptide repeat and a U-box that functions as a ubiquitin ligase/cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA polymerase beta (Polb), among other targets. Mutations in this gene cause spinocerebellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2. [provided by RefSeq, Jun 2014]","start":680224,"end":682870,"strand":1,"description":"STIP1 homology and U-box containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11427]"}, {"versioned_ensembl_gene_id":"ENSG00000269043.1","gene_symbol":"AC008554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20432552,"end":20528615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268272.1","gene_symbol":"VN1R78P","gene_name":"vomeronasal 1 receptor 78 pseudogene [Source:HGNC Symbol;Acc:HGNC:37399]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312823","summary":null,"start":20583084,"end":20583647,"strand":-1,"description":"vomeronasal 1 receptor 78 pseudogene [Source:HGNC Symbol;Acc:HGNC:37399]"}, {"versioned_ensembl_gene_id":"ENSG00000214825.2","gene_symbol":"EI24P3","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131881","summary":null,"start":44524744,"end":44525805,"strand":-1,"description":"EI24, autophagy associated transmembrane protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44588]"}, {"versioned_ensembl_gene_id":"ENSG00000092020.10","gene_symbol":"PPP2R3C","gene_name":"protein phosphatase 2 regulatory subunit B''gamma [Source:HGNC Symbol;Acc:HGNC:17485]","synonyms":"G5PR,G4-1,FLJ20644,C14orf10","biotype":"protein_coding","ncbi_id":"55012","summary":"This gene encodes a regulatory subunit of the serine/threonine phosphatase, protein phosphatase 2. This protein is localized to both nuclear and cytoplasmic regions depending on cell cycle phase. Homozygous conditional knockout mice for this gene exhibit reduced numbers and impaired proliferation of immune system B cells. This protein may regulate the expression of the P-glycoprotein ATP-binding cassette transporter through its phosphatase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":35085467,"end":35122517,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B''gamma [Source:HGNC Symbol;Acc:HGNC:17485]"}, {"versioned_ensembl_gene_id":"ENSG00000069966.18","gene_symbol":"GNB5","gene_name":"G protein subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:4401]","synonyms":"GB5","biotype":"protein_coding","ncbi_id":"10681","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. Alternatively spliced transcript variants encoding different isoforms exist. [provided by RefSeq, Jul 2008]","start":52115105,"end":52191369,"strand":-1,"description":"G protein subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:4401]"}, {"versioned_ensembl_gene_id":"ENSG00000280331.1","gene_symbol":"AC061999.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36510361,"end":36510537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239671.1","gene_symbol":"AC100793.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42714299,"end":42714643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259709.1","gene_symbol":"AC023906.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52124561,"end":52140246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259327.1","gene_symbol":"AC023906.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52116574,"end":52122131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117009.11","gene_symbol":"KMO","gene_name":"kynurenine 3-monooxygenase [Source:HGNC Symbol;Acc:HGNC:6381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8564","summary":"This gene encodes a mitochondrion outer membrane protein that catalyzes the hydroxylation of L-tryptophan metabolite, L-kynurenine, to form L-3-hydroxykynurenine. Studies in yeast identified this gene as a therapeutic target for Huntington disease. [provided by RefSeq, Oct 2011]","start":241532134,"end":241595642,"strand":1,"description":"kynurenine 3-monooxygenase [Source:HGNC Symbol;Acc:HGNC:6381]"}, {"versioned_ensembl_gene_id":"ENSG00000244527.1","gene_symbol":"AC022795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21119182,"end":21119661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229117.8","gene_symbol":"RPL41","gene_name":"ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:10354]","synonyms":"L41","biotype":"protein_coding","ncbi_id":"6171","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which shares sequence similarity with the yeast ribosomal protein YL41, belongs to the L41E family of ribosomal proteins. It is located in the cytoplasm. The protein can interact with the beta subunit of protein kinase CKII and can stimulate the phosphorylation of DNA topoisomerase II-alpha by CKII. Two alternative splice variants have been identified, both encoding the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":56116586,"end":56117943,"strand":1,"description":"ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:10354]"}, {"versioned_ensembl_gene_id":"ENSG00000225026.1","gene_symbol":"AC091492.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12328003,"end":12328274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233605.2","gene_symbol":"LINC01851","gene_name":"long intergenic non-protein coding RNA 1851 [Source:HGNC Symbol;Acc:HGNC:52667]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927926","summary":null,"start":77915934,"end":77918011,"strand":1,"description":"long intergenic non-protein coding RNA 1851 [Source:HGNC Symbol;Acc:HGNC:52667]"}, {"versioned_ensembl_gene_id":"ENSG00000260920.2","gene_symbol":"AL031985.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":40464319,"end":40466767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250456.1","gene_symbol":"LINC02260","gene_name":"long intergenic non-protein coding RNA 2260 [Source:HGNC Symbol;Acc:HGNC:27956]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339978","summary":null,"start":54603211,"end":54607131,"strand":-1,"description":"long intergenic non-protein coding RNA 2260 [Source:HGNC Symbol;Acc:HGNC:27956]"}, {"versioned_ensembl_gene_id":"ENSG00000251264.1","gene_symbol":"AC098868.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54440502,"end":54446723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229924.3","gene_symbol":"FAM90A26","gene_name":"family with sequence similarity 90 member A26 [Source:HGNC Symbol;Acc:HGNC:43746]","synonyms":"FAM90A26P","biotype":"protein_coding","ncbi_id":"100287045","summary":null,"start":9170409,"end":9176730,"strand":1,"description":"family with sequence similarity 90 member A26 [Source:HGNC Symbol;Acc:HGNC:43746]"}, {"versioned_ensembl_gene_id":"ENSG00000137878.16","gene_symbol":"GCOM1","gene_name":"GRINL1A complex locus 1 [Source:HGNC Symbol;Acc:HGNC:26424]","synonyms":"MYZAP-POLR2M,GRINL1A,FLJ30973","biotype":"protein_coding","ncbi_id":"145781","summary":"This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]","start":57591908,"end":57714745,"strand":1,"description":"GRINL1A complex locus 1 [Source:HGNC Symbol;Acc:HGNC:26424]"}, {"versioned_ensembl_gene_id":"ENSG00000269885.1","gene_symbol":"VN1R79P","gene_name":"vomeronasal 1 receptor 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:37400]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312824","summary":null,"start":20758440,"end":20758952,"strand":1,"description":"vomeronasal 1 receptor 79 pseudogene [Source:HGNC Symbol;Acc:HGNC:37400]"}, {"versioned_ensembl_gene_id":"ENSG00000237725.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"OR2I3P,HS6M1-14,OR2I2,OR2I4P,OR2I1","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29553169,"end":29554116,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000269110.1","gene_symbol":"AC010636.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20553792,"end":20661583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269040.1","gene_symbol":"BNIP3P24","gene_name":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421698","summary":null,"start":20784596,"end":20785152,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]"}, {"versioned_ensembl_gene_id":"ENSG00000233030.2","gene_symbol":"AC243772.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149785659,"end":149793020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164081.12","gene_symbol":"TEX264","gene_name":"testis expressed 264 [Source:HGNC Symbol;Acc:HGNC:30247]","synonyms":"ZSIG11,FLJ13935","biotype":"protein_coding","ncbi_id":"51368","summary":null,"start":51662693,"end":51704323,"strand":1,"description":"testis expressed 264 [Source:HGNC Symbol;Acc:HGNC:30247]"}, {"versioned_ensembl_gene_id":"ENSG00000083896.12","gene_symbol":"YTHDC1","gene_name":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]","synonyms":"YT521-B,YT521,KIAA1966","biotype":"protein_coding","ncbi_id":"91746","summary":null,"start":68310387,"end":68350089,"strand":-1,"description":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]"}, {"versioned_ensembl_gene_id":"ENSG00000253960.1","gene_symbol":"AC016885.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93215925,"end":93234878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269373.1","gene_symbol":"AC008739.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20838515,"end":20847417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251638.1","gene_symbol":"AC006390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24768049,"end":24768331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280171.1","gene_symbol":"AC010329.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20674923,"end":20696533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177306.4","gene_symbol":"OR7E125P","gene_name":"olfactory receptor family 7 subfamily E member 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:15098]","synonyms":"PJCG6","biotype":"unprocessed_pseudogene","ncbi_id":"389616","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7246726,"end":7247571,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:15098]"}, {"versioned_ensembl_gene_id":"ENSG00000268461.2","gene_symbol":"AC078899.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20389658,"end":20390689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144119.3","gene_symbol":"C1QL2","gene_name":"complement C1q like 2 [Source:HGNC Symbol;Acc:HGNC:24181]","synonyms":"CTRP10,C1QTNF10","biotype":"protein_coding","ncbi_id":"165257","summary":null,"start":119156243,"end":119158889,"strand":-1,"description":"complement C1q like 2 [Source:HGNC Symbol;Acc:HGNC:24181]"}, {"versioned_ensembl_gene_id":"ENSG00000105974.11","gene_symbol":"CAV1","gene_name":"caveolin 1 [Source:HGNC Symbol;Acc:HGNC:1527]","synonyms":"CAV","biotype":"protein_coding","ncbi_id":"857","summary":"The scaffolding protein encoded by this gene is the main component of the caveolae plasma membranes found in most cell types. The protein links integrin subunits to the tyrosine kinase FYN, an initiating step in coupling integrins to the Ras-ERK pathway and promoting cell cycle progression. The gene is a tumor suppressor gene candidate and a negative regulator of the Ras-p42/44 mitogen-activated kinase cascade. Caveolin 1 and caveolin 2 are located next to each other on chromosome 7 and express colocalizing proteins that form a stable hetero-oligomeric complex. Mutations in this gene have been associated with Berardinelli-Seip congenital lipodystrophy. Alternatively spliced transcripts encode alpha and beta isoforms of caveolin 1.[provided by RefSeq, Mar 2010]","start":116524785,"end":116561184,"strand":1,"description":"caveolin 1 [Source:HGNC Symbol;Acc:HGNC:1527]"}, {"versioned_ensembl_gene_id":"ENSG00000150337.13","gene_symbol":"FCGR1A","gene_name":"Fc fragment of IgG receptor Ia [Source:HGNC Symbol;Acc:HGNC:3613]","synonyms":"CD64,CD64A","biotype":"protein_coding","ncbi_id":"2209","summary":"This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1. [provided by RefSeq, Jul 2008]","start":149782671,"end":149792518,"strand":1,"description":"Fc fragment of IgG receptor Ia [Source:HGNC Symbol;Acc:HGNC:3613]"}, {"versioned_ensembl_gene_id":"ENSG00000116209.11","gene_symbol":"TMEM59","gene_name":"transmembrane protein 59 [Source:HGNC Symbol;Acc:HGNC:1239]","synonyms":"HSPC001,C1orf8","biotype":"protein_coding","ncbi_id":"9528","summary":"This gene encodes a protein shown to regulate autophagy in response to bacterial infection. This protein may also regulate the retention of amyloid precursor protein (APP) in the Golgi apparatus through its control of APP glycosylation. Overexpression of this protein has been found to promote apoptosis in a glioma cell line. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":54026681,"end":54053504,"strand":-1,"description":"transmembrane protein 59 [Source:HGNC Symbol;Acc:HGNC:1239]"}, {"versioned_ensembl_gene_id":"ENSG00000247911.3","gene_symbol":"HMGN1P12","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480725","summary":null,"start":71537652,"end":71537846,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]"}, {"versioned_ensembl_gene_id":"ENSG00000280378.1","gene_symbol":"AL353898.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":54033126,"end":54034880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257246.1","gene_symbol":"PHBP19","gene_name":"prohibitin pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"494150","summary":null,"start":51124628,"end":51125381,"strand":-1,"description":"prohibitin pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51552]"}, {"versioned_ensembl_gene_id":"ENSG00000100890.15","gene_symbol":"KIAA0391","gene_name":"KIAA0391 [Source:HGNC Symbol;Acc:HGNC:19958]","synonyms":"PRORP,MRPP3","biotype":"protein_coding","ncbi_id":"9692","summary":null,"start":35121846,"end":35277614,"strand":1,"description":"KIAA0391 [Source:HGNC Symbol;Acc:HGNC:19958]"}, {"versioned_ensembl_gene_id":"ENSG00000162843.17","gene_symbol":"WDR64","gene_name":"WD repeat domain 64 [Source:HGNC Symbol;Acc:HGNC:26570]","synonyms":"FLJ32978","biotype":"protein_coding","ncbi_id":"128025","summary":null,"start":241652278,"end":241802133,"strand":1,"description":"WD repeat domain 64 [Source:HGNC Symbol;Acc:HGNC:26570]"}, {"versioned_ensembl_gene_id":"ENSG00000262227.1","gene_symbol":"AC004771.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4987706,"end":4988446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278595.1","gene_symbol":"AL133396.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4761300,"end":4761696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259090.1","gene_symbol":"AL121594.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35157904,"end":35159099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114948.12","gene_symbol":"ADAM23","gene_name":"ADAM metallopeptidase domain 23 [Source:HGNC Symbol;Acc:HGNC:202]","synonyms":"MDC3","biotype":"protein_coding","ncbi_id":"8745","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. It is reported that inactivation of this gene is associated with tumorigenesis in human cancers. [provided by RefSeq, May 2013]","start":206443539,"end":206621130,"strand":1,"description":"ADAM metallopeptidase domain 23 [Source:HGNC Symbol;Acc:HGNC:202]"}, {"versioned_ensembl_gene_id":"ENSG00000240392.1","gene_symbol":"AL121594.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35262462,"end":35263036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184905.8","gene_symbol":"TCEAL2","gene_name":"transcription elongation factor A like 2 [Source:HGNC Symbol;Acc:HGNC:29818]","synonyms":"WEX1,MY0876G05,my048","biotype":"protein_coding","ncbi_id":"140597","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. [provided by RefSeq, Jul 2008]","start":102125688,"end":102127711,"strand":1,"description":"transcription elongation factor A like 2 [Source:HGNC Symbol;Acc:HGNC:29818]"}, {"versioned_ensembl_gene_id":"ENSG00000262429.1","gene_symbol":"AC004771.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4967995,"end":4968822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234503.1","gene_symbol":"AP000550.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21177892,"end":21179875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125703.14","gene_symbol":"ATG4C","gene_name":"autophagy related 4C cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16040]","synonyms":"FLJ14867,AUTL3,AUTL1,APG4C","biotype":"protein_coding","ncbi_id":"84938","summary":"Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Alternate transcriptional splice variants, encoding the same protein, have been characterized. [provided by RefSeq, Jul 2008]","start":62784135,"end":62865513,"strand":1,"description":"autophagy related 4C cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16040]"}, {"versioned_ensembl_gene_id":"ENSG00000205579.3","gene_symbol":"DYNLL1P1","gene_name":"dynein light chain LC8-type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20723]","synonyms":"DNCL1P1","biotype":"processed_pseudogene","ncbi_id":"246720","summary":null,"start":81246295,"end":81246563,"strand":-1,"description":"dynein light chain LC8-type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20723]"}, {"versioned_ensembl_gene_id":"ENSG00000197632.8","gene_symbol":"SERPINB2","gene_name":"serpin family B member 2 [Source:HGNC Symbol;Acc:HGNC:8584]","synonyms":"HsT1201,PLANH2,PAI2","biotype":"protein_coding","ncbi_id":"5055","summary":null,"start":63871692,"end":63903890,"strand":1,"description":"serpin family B member 2 [Source:HGNC Symbol;Acc:HGNC:8584]"}, {"versioned_ensembl_gene_id":"ENSG00000270871.1","gene_symbol":"AC015849.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35816717,"end":35830293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274082.1","gene_symbol":"AC245128.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254834.4","gene_symbol":"OR5M10","gene_name":"olfactory receptor family 5 subfamily M member 10 [Source:HGNC Symbol;Acc:HGNC:15290]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390167","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56576736,"end":56577787,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 10 [Source:HGNC Symbol;Acc:HGNC:15290]"}, {"versioned_ensembl_gene_id":"ENSG00000255223.4","gene_symbol":"OR5M11","gene_name":"olfactory receptor family 5 subfamily M member 11 [Source:HGNC Symbol;Acc:HGNC:15291]","synonyms":"OR11-199","biotype":"protein_coding","ncbi_id":"219487","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56542262,"end":56543281,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 11 [Source:HGNC Symbol;Acc:HGNC:15291]"}, {"versioned_ensembl_gene_id":"ENSG00000234502.2","gene_symbol":"FYTTD1P1","gene_name":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128665","summary":null,"start":101375344,"end":101376603,"strand":-1,"description":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]"}, {"versioned_ensembl_gene_id":"ENSG00000228400.1","gene_symbol":"AC079154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124016858,"end":124025173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250503.1","gene_symbol":"AC093831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130881027,"end":130885641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280059.1","gene_symbol":"AC093831.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130808507,"end":130811933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188343.12","gene_symbol":"FAM92A","gene_name":"family with sequence similarity 92 member A [Source:HGNC Symbol;Acc:HGNC:30452]","synonyms":"FLJ38979,FAM92A1","biotype":"protein_coding","ncbi_id":"137392","summary":null,"start":93698561,"end":93731527,"strand":1,"description":"family with sequence similarity 92 member A [Source:HGNC Symbol;Acc:HGNC:30452]"}, {"versioned_ensembl_gene_id":"ENSG00000249018.2","gene_symbol":"GAPDHP56","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:38562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421232","summary":null,"start":130503357,"end":130504344,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:38562]"}, {"versioned_ensembl_gene_id":"ENSG00000253854.1","gene_symbol":"AC010834.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93719574,"end":93721167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269586.7","gene_symbol":"CT45A10","gene_name":"cancer/testis antigen family 45 member A10 [Source:HGNC Symbol;Acc:HGNC:51263]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723631","summary":null,"start":135881063,"end":135889086,"strand":-1,"description":"cancer/testis antigen family 45 member A10 [Source:HGNC Symbol;Acc:HGNC:51263]"}, {"versioned_ensembl_gene_id":"ENSG00000235020.4","gene_symbol":"AL390783.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18206127,"end":18261194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118402.5","gene_symbol":"ELOVL4","gene_name":"ELOVL fatty acid elongase 4 [Source:HGNC Symbol;Acc:HGNC:14415]","synonyms":"STGD3,STGD2,SCA34,CT118","biotype":"protein_coding","ncbi_id":"6785","summary":"This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul 2008]","start":79914812,"end":79947580,"strand":-1,"description":"ELOVL fatty acid elongase 4 [Source:HGNC Symbol;Acc:HGNC:14415]"}, {"versioned_ensembl_gene_id":"ENSG00000148053.15","gene_symbol":"NTRK2","gene_name":"neurotrophic receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:8032]","synonyms":"TRKB","biotype":"protein_coding","ncbi_id":"4915","summary":"This gene encodes a member of the neurotrophic tyrosine receptor kinase (NTRK) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. Signalling through this kinase leads to cell differentiation. Mutations in this gene have been associated with obesity and mood disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":84668551,"end":85027070,"strand":1,"description":"neurotrophic receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:8032]"}, {"versioned_ensembl_gene_id":"ENSG00000254603.1","gene_symbol":"OR5M6P","gene_name":"olfactory receptor family 5 subfamily M member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14814]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79512","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56512235,"end":56513171,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14814]"}, {"versioned_ensembl_gene_id":"ENSG00000110721.11","gene_symbol":"CHKA","gene_name":"choline kinase alpha [Source:HGNC Symbol;Acc:HGNC:1937]","synonyms":"CKI,CHK","biotype":"protein_coding","ncbi_id":"1119","summary":"The major pathway for the biosynthesis of phosphatidylcholine occurs via the CDP-choline pathway. The protein encoded by this gene is the initial enzyme in the sequence and may play a regulatory role. The encoded protein also catalyzes the phosphorylation of ethanolamine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68052859,"end":68121444,"strand":-1,"description":"choline kinase alpha [Source:HGNC Symbol;Acc:HGNC:1937]"}, {"versioned_ensembl_gene_id":"ENSG00000231071.1","gene_symbol":"AL133396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4735669,"end":4736673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270946.5","gene_symbol":"CT45A9","gene_name":"cancer/testis antigen family 45 member A9 [Source:HGNC Symbol;Acc:HGNC:51262]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723680","summary":null,"start":135863776,"end":135871812,"strand":-1,"description":"cancer/testis antigen family 45 member A9 [Source:HGNC Symbol;Acc:HGNC:51262]"}, {"versioned_ensembl_gene_id":"ENSG00000255031.5","gene_symbol":"AP002807.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68050740,"end":68053762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188004.9","gene_symbol":"SNHG28","gene_name":"small nucleolar RNA host gene 28 [Source:HGNC Symbol;Acc:HGNC:27647]","synonyms":"VSIG8-OT1,FLJ39187,C1orf204","biotype":"protein_coding","ncbi_id":"284677","summary":null,"start":159834474,"end":159855347,"strand":-1,"description":"small nucleolar RNA host gene 28 [Source:HGNC Symbol;Acc:HGNC:27647]"}, {"versioned_ensembl_gene_id":"ENSG00000253722.1","gene_symbol":"AC010834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93733216,"end":93734022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253781.1","gene_symbol":"ZNF317P1","gene_name":"zinc finger protein 317 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288659","summary":null,"start":93646066,"end":93647092,"strand":1,"description":"zinc finger protein 317 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31062]"}, {"versioned_ensembl_gene_id":"ENSG00000056586.15","gene_symbol":"RC3H2","gene_name":"ring finger and CCCH-type domains 2 [Source:HGNC Symbol;Acc:HGNC:21461]","synonyms":"RNF164,MNAB,FLJ20713,FLJ20301","biotype":"protein_coding","ncbi_id":"54542","summary":null,"start":122844556,"end":122905341,"strand":-1,"description":"ring finger and CCCH-type domains 2 [Source:HGNC Symbol;Acc:HGNC:21461]"}, {"versioned_ensembl_gene_id":"ENSG00000276074.1","gene_symbol":"SOX2OT_exon1","gene_name":"SOX2 overlapping transcript exon 1 [Source:RFAM;Acc:RF01951]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":181610498,"end":181610729,"strand":1,"description":"SOX2 overlapping transcript exon 1 [Source:RFAM;Acc:RF01951]"}, {"versioned_ensembl_gene_id":"ENSG00000108799.12","gene_symbol":"EZH1","gene_name":"enhancer of zeste 1 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3526]","synonyms":"KMT6B,KIAA0388","biotype":"protein_coding","ncbi_id":"2145","summary":"EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008 [PubMed 19026780]).[supplied by OMIM, Mar 2009]","start":42700275,"end":42745049,"strand":-1,"description":"enhancer of zeste 1 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3526]"}, {"versioned_ensembl_gene_id":"ENSG00000241058.3","gene_symbol":"NSUN6","gene_name":"NOP2/Sun RNA methyltransferase family member 6 [Source:HGNC Symbol;Acc:HGNC:23529]","synonyms":"NOPD1,FLJ23743,ARL5B-AS1","biotype":"protein_coding","ncbi_id":"221078","summary":null,"start":18545561,"end":18659285,"strand":-1,"description":"NOP2/Sun RNA methyltransferase family member 6 [Source:HGNC Symbol;Acc:HGNC:23529]"}, {"versioned_ensembl_gene_id":"ENSG00000163380.15","gene_symbol":"LMOD3","gene_name":"leiomodin 3 [Source:HGNC Symbol;Acc:HGNC:6649]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56203","summary":"The protein encoded by this gene is a member of the leiomodin family of proteins. This protein contains three actin-binding domains, a tropomyosin domain, a leucine-rich repeat domain, and a Wiskott-Aldrich syndrome protein homology 2 domain (WH2). Localization of this protein to the pointed ends of thin filaments has been observed, and there is evidence that this protein acts as a catalyst of actin nucleation, and is important to the organization of sarcomeric thin filaments in skeletal muscles. Mutations in this gene have been associated as one cause of Nemaline myopathy, as other genes have also been linked to this disorder. Nemaline myopathy is a disorder characterized by nonprogressive generalized muscle weakness and protein inclusions (nemaline bodies) in skeletal myofibers. Patients with mutations in this gene often present with a severe congenital form of the disorder. [provided by RefSeq, Jan 2015]","start":69106872,"end":69123032,"strand":-1,"description":"leiomodin 3 [Source:HGNC Symbol;Acc:HGNC:6649]"}, {"versioned_ensembl_gene_id":"ENSG00000273696.4","gene_symbol":"CT45A7","gene_name":"cancer/testis antigen family 45 member A7 [Source:HGNC Symbol;Acc:HGNC:51260]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060211","summary":null,"start":135829247,"end":135837268,"strand":-1,"description":"cancer/testis antigen family 45 member A7 [Source:HGNC Symbol;Acc:HGNC:51260]"}, {"versioned_ensembl_gene_id":"ENSG00000254902.1","gene_symbol":"ANO1-AS1","gene_name":"ANO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40016]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873981","summary":null,"start":70187788,"end":70188509,"strand":-1,"description":"ANO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40016]"}, {"versioned_ensembl_gene_id":"ENSG00000227738.1","gene_symbol":"AC092646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123762171,"end":123763071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260851.6","gene_symbol":"AC010542.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66469812,"end":66517312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267868.1","gene_symbol":"AL356740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112964835,"end":112966131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225313.5","gene_symbol":"AL513327.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33307348,"end":33349245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271449.7","gene_symbol":"CT45A2","gene_name":"cancer/testis antigen family 45 member A2 [Source:HGNC Symbol;Acc:HGNC:28400]","synonyms":"CT45.2,CT45-2","biotype":"protein_coding","ncbi_id":"728911","summary":"This gene represents one of a cluster of several similar genes located on the q arm of chromosome X. The genes in this cluster encode members of the cancer/testis (CT) family of antigens, and are distinct from other CT antigens. These antigens are thought to be novel therapeutic targets for human cancers. [provided by RefSeq, Apr 2014]","start":135811668,"end":135820012,"strand":-1,"description":"cancer/testis antigen family 45 member A2 [Source:HGNC Symbol;Acc:HGNC:28400]"}, {"versioned_ensembl_gene_id":"ENSG00000171864.4","gene_symbol":"PRND","gene_name":"prion like protein doppel [Source:HGNC Symbol;Acc:HGNC:15748]","synonyms":"PrPLP,DPL,DOPPEL,dJ1068H6.4","biotype":"protein_coding","ncbi_id":"23627","summary":"This gene is found on chromosome 20, approximately 20 kbp downstream of the gene encoding cellular prion protein, to which it is biochemically and structurally similar. The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that is found predominantly in testis. Mutations in this gene may lead to neurological disorders. [provided by RefSeq, Jul 2008]","start":4721910,"end":4728460,"strand":1,"description":"prion like protein doppel [Source:HGNC Symbol;Acc:HGNC:15748]"}, {"versioned_ensembl_gene_id":"ENSG00000125877.12","gene_symbol":"ITPA","gene_name":"inosine triphosphatase [Source:HGNC Symbol;Acc:HGNC:6176]","synonyms":"HLC14-06-P,dJ794I6.3,C20orf37","biotype":"protein_coding","ncbi_id":"3704","summary":"This gene encodes an inosine triphosphate pyrophosphohydrolase. The encoded protein hydrolyzes inosine triphosphate and deoxyinosine triphosphate to the monophosphate nucleotide and diphosphate. This protein, which is a member of the HAM1 NTPase protein family, is found in the cytoplasm and acts as a homodimer. Defects in the encoded protein can result in inosine triphosphate pyrophosphorylase deficiency which causes an accumulation of ITP in red blood cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":3208868,"end":3223870,"strand":1,"description":"inosine triphosphatase [Source:HGNC Symbol;Acc:HGNC:6176]"}, {"versioned_ensembl_gene_id":"ENSG00000257524.5","gene_symbol":"AL157935.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":127867864,"end":127886787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254912.2","gene_symbol":"AC135983.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32494003,"end":32500346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277147.4","gene_symbol":"LINC00869","gene_name":"long intergenic non-protein coding RNA 869 [Source:HGNC Symbol;Acc:HGNC:29050]","synonyms":"KIAA0493","biotype":"lincRNA","ncbi_id":"57234","summary":null,"start":149606334,"end":149679523,"strand":1,"description":"long intergenic non-protein coding RNA 869 [Source:HGNC Symbol;Acc:HGNC:29050]"}, {"versioned_ensembl_gene_id":"ENSG00000261375.1","gene_symbol":"AC135983.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32489267,"end":32491586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261519.3","gene_symbol":"AC010542.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66549280,"end":66551189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280113.2","gene_symbol":"AL357140.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":9826289,"end":9828271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283787.1","gene_symbol":"AC051649.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1888577,"end":1891895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158985.13","gene_symbol":"CDC42SE2","gene_name":"CDC42 small effector 2 [Source:HGNC Symbol;Acc:HGNC:18547]","synonyms":"SPEC2,FLJ21967","biotype":"protein_coding","ncbi_id":"56990","summary":null,"start":131245493,"end":131398447,"strand":1,"description":"CDC42 small effector 2 [Source:HGNC Symbol;Acc:HGNC:18547]"}, {"versioned_ensembl_gene_id":"ENSG00000279370.1","gene_symbol":"AC004777.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131261321,"end":131261607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270789.1","gene_symbol":"AC135983.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32461666,"end":32461809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100902.10","gene_symbol":"PSMA6","gene_name":"proteasome subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:9535]","synonyms":"PROS27,p27K,MGC23846,MGC2333,MGC22756,IOTA","biotype":"protein_coding","ncbi_id":"5687","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Multiple transcript variants encoding several different isoforms have been found for this gene. A pseudogene has been identified on the Y chromosome. [provided by RefSeq, Aug 2013]","start":35278633,"end":35317493,"strand":1,"description":"proteasome subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:9535]"}, {"versioned_ensembl_gene_id":"ENSG00000261656.5","gene_symbol":"BEAN1-AS1","gene_name":"BEAN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51114]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927726","summary":null,"start":66469796,"end":66481230,"strand":-1,"description":"BEAN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51114]"}, {"versioned_ensembl_gene_id":"ENSG00000174498.13","gene_symbol":"IGDCC3","gene_name":"immunoglobulin superfamily DCC subclass member 3 [Source:HGNC Symbol;Acc:HGNC:9700]","synonyms":"PUNC,HsT18880","biotype":"protein_coding","ncbi_id":"9543","summary":null,"start":65327127,"end":65378040,"strand":-1,"description":"immunoglobulin superfamily DCC subclass member 3 [Source:HGNC Symbol;Acc:HGNC:9700]"}, {"versioned_ensembl_gene_id":"ENSG00000220918.1","gene_symbol":"AL132875.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79854684,"end":79855632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257337.6","gene_symbol":"AC068888.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53014596,"end":53054438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270115.1","gene_symbol":"AL513327.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33261212,"end":33261680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264023.1","gene_symbol":"AC068418.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21457434,"end":21458989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165178.9","gene_symbol":"NCF1C","gene_name":"neutrophil cytosolic factor 1C pseudogene [Source:HGNC Symbol;Acc:HGNC:32523]","synonyms":"SH3PXD1C","biotype":"unprocessed_pseudogene","ncbi_id":"654817","summary":"The neutrophil cytosolic factor 1 (NCF1) gene encodes the 47 kDa cytosolic subunit of neutrophil NADPH oxidase, which produces superoxide anion. The NCF1 gene is located in close proximity to two highly similar, multi-exon pseudogenes at chromosome 7q11.23, corresponding to this gene record and GeneID:654816. The two pseudogenes contain a dinucleotide deletion (delta-GT) in exon 2 that results in a frameshift and truncation of the open reading frame, and neither pseudogene is likely to express a protein. Recombination events between the pseudogenes and the functional NCF1 gene can inactivate the NCF1 gene and result in chronic granulomatous disease. [provided by RefSeq, Nov 2009]","start":75156639,"end":75172044,"strand":-1,"description":"neutrophil cytosolic factor 1C pseudogene [Source:HGNC Symbol;Acc:HGNC:32523]"}, {"versioned_ensembl_gene_id":"ENSG00000250268.3","gene_symbol":"ALG1L14P","gene_name":"asparagine-linked glycosylation 1-like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44383]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996649","summary":null,"start":9166297,"end":9170270,"strand":-1,"description":"asparagine-linked glycosylation 1-like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44383]"}, {"versioned_ensembl_gene_id":"ENSG00000230968.1","gene_symbol":"AC084149.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77672215,"end":77673792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263464.2","gene_symbol":"PPIAL4C","gene_name":"peptidylprolyl isomerase A like 4C [Source:HGNC Symbol;Acc:HGNC:33995]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653598","summary":null,"start":149583865,"end":149584464,"strand":1,"description":"peptidylprolyl isomerase A like 4C [Source:HGNC Symbol;Acc:HGNC:33995]"}, {"versioned_ensembl_gene_id":"ENSG00000271392.1","gene_symbol":"AC006237.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35757199,"end":35758325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238100.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33073573,"end":33076557,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000050748.17","gene_symbol":"MAPK9","gene_name":"mitogen-activated protein kinase 9 [Source:HGNC Symbol;Acc:HGNC:6886]","synonyms":"SAPK,PRKM9,p54a,JNK2","biotype":"protein_coding","ncbi_id":"5601","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase targets specific transcription factors, and thus mediates immediate-early gene expression in response to various cell stimuli. It is most closely related to MAPK8, both of which are involved in UV radiation induced apoptosis, thought to be related to the cytochrome c-mediated cell death pathway. This gene and MAPK8 are also known as c-Jun N-terminal kinases. This kinase blocks the ubiquitination of tumor suppressor p53, and thus it increases the stability of p53 in nonstressed cells. Studies of this gene's mouse counterpart suggest a key role in T-cell differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Sep 2008]","start":180233143,"end":180292099,"strand":-1,"description":"mitogen-activated protein kinase 9 [Source:HGNC Symbol;Acc:HGNC:6886]"}, {"versioned_ensembl_gene_id":"ENSG00000237856.1","gene_symbol":"AC062020.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123065321,"end":123067722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171236.9","gene_symbol":"LRG1","gene_name":"leucine rich alpha-2-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:29480]","synonyms":"LRG","biotype":"protein_coding","ncbi_id":"116844","summary":"The leucine-rich repeat (LRR) family of proteins, including LRG1, have been shown to be involved in protein-protein interaction, signal transduction, and cell adhesion and development. LRG1 is expressed during granulocyte differentiation (O'Donnell et al., 2002 [PubMed 12223515]).[supplied by OMIM, Mar 2008]","start":4536409,"end":4540474,"strand":-1,"description":"leucine rich alpha-2-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:29480]"}, {"versioned_ensembl_gene_id":"ENSG00000162517.12","gene_symbol":"PEF1","gene_name":"penta-EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30009]","synonyms":"PEF1A","biotype":"protein_coding","ncbi_id":"553115","summary":"This gene encodes a calcium-binding protein belonging to the penta-EF-hand protein family. The encoded protein has been shown to form a heterodimer with the programmed cell death 6 gene product and may modulate its function in Ca(2+) signaling. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 1.[provided by RefSeq, May 2010]","start":31629862,"end":31644896,"strand":-1,"description":"penta-EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30009]"}, {"versioned_ensembl_gene_id":"ENSG00000213431.4","gene_symbol":"AC080014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100910975,"end":100912175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158714.10","gene_symbol":"SLAMF8","gene_name":"SLAM family member 8 [Source:HGNC Symbol;Acc:HGNC:21391]","synonyms":"CD353,BLAME,SBBI42","biotype":"protein_coding","ncbi_id":"56833","summary":"This gene encodes a member of the CD2 family of cell surface proteins involved in lymphocyte activation. These proteins are characterized by Ig domains. This protein is expressed in lymphoid tissues, and studies of a similar protein in mouse suggest that it may function during B cell lineage commitment. The gene is found in a region of chromosome 1 containing many CD2 genes. [provided by RefSeq, Jul 2008]","start":159826750,"end":159837249,"strand":1,"description":"SLAM family member 8 [Source:HGNC Symbol;Acc:HGNC:21391]"}, {"versioned_ensembl_gene_id":"ENSG00000259621.1","gene_symbol":"AC069029.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98880659,"end":98893535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279067.1","gene_symbol":"AC002540.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96118647,"end":96119995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279135.1","gene_symbol":"AL512652.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20712431,"end":20714146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229721.3","gene_symbol":"AC104115.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180226378,"end":180227000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284677.1","gene_symbol":"AL031985.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40436199,"end":40450039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278291.1","gene_symbol":"AL161772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20699307,"end":20703718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235790.7","gene_symbol":"AC114488.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31644049,"end":31660162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267385.1","gene_symbol":"AC011498.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4528427,"end":4540067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183571.10","gene_symbol":"PGPEP1L","gene_name":"pyroglutamyl-peptidase I-like [Source:HGNC Symbol;Acc:HGNC:27080]","synonyms":null,"biotype":"protein_coding","ncbi_id":"145814","summary":null,"start":98968230,"end":99007795,"strand":-1,"description":"pyroglutamyl-peptidase I-like [Source:HGNC Symbol;Acc:HGNC:27080]"}, {"versioned_ensembl_gene_id":"ENSG00000150456.10","gene_symbol":"EEF1AKMT1","gene_name":"EEF1A lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27351]","synonyms":"N6AMT2","biotype":"protein_coding","ncbi_id":"221143","summary":null,"start":20728731,"end":20773958,"strand":-1,"description":"EEF1A lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27351]"}, {"versioned_ensembl_gene_id":"ENSG00000256342.1","gene_symbol":"LINC02359","gene_name":"long intergenic non-protein coding RNA 2359 [Source:HGNC Symbol;Acc:HGNC:53280]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927464","summary":null,"start":126095992,"end":126103935,"strand":1,"description":"long intergenic non-protein coding RNA 2359 [Source:HGNC Symbol;Acc:HGNC:53280]"}, {"versioned_ensembl_gene_id":"ENSG00000121764.11","gene_symbol":"HCRTR1","gene_name":"hypocretin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4848]","synonyms":"OX1R","biotype":"protein_coding","ncbi_id":"3061","summary":"The protein encoded by this gene is a G-protein coupled receptor involved in the regulation of feeding behavior. The encoded protein selectively binds the hypothalamic neuropeptide orexin A. A related gene (HCRTR2) encodes a G-protein coupled receptor that binds orexin A and orexin B. [provided by RefSeq, Jan 2009]","start":31617686,"end":31632518,"strand":1,"description":"hypocretin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4848]"}, {"versioned_ensembl_gene_id":"ENSG00000220515.2","gene_symbol":"PGAM1P10","gene_name":"phosphoglycerate mutase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420633","summary":null,"start":73055097,"end":73055857,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42457]"}, {"versioned_ensembl_gene_id":"ENSG00000172458.4","gene_symbol":"IL17D","gene_name":"interleukin 17D [Source:HGNC Symbol;Acc:HGNC:5984]","synonyms":"IL27,IL-27,IL-22,IL-17D,FLJ30846","biotype":"protein_coding","ncbi_id":"53342","summary":"The protein encoded by this gene is a cytokine that shares the sequence similarity with IL17. The treatment of endothelial cells with this cytokine has been shown to stimulate the production of other cytokines including IL6, IL8 and CSF2/ GM-CSF. The increased expression of IL8 induced by this cytokine was found to be NF-kappa B-dependent. [provided by RefSeq, Jul 2008]","start":20702127,"end":20723098,"strand":1,"description":"interleukin 17D [Source:HGNC Symbol;Acc:HGNC:5984]"}, {"versioned_ensembl_gene_id":"ENSG00000176268.5","gene_symbol":"CYCSP34","gene_name":"cytochrome c, somatic pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:24408]","synonyms":"HCP34","biotype":"processed_pseudogene","ncbi_id":"360182","summary":null,"start":40863599,"end":40863902,"strand":-1,"description":"cytochrome c, somatic pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:24408]"}, {"versioned_ensembl_gene_id":"ENSG00000089280.18","gene_symbol":"FUS","gene_name":"FUS RNA binding protein [Source:HGNC Symbol;Acc:HGNC:4010]","synonyms":"HNRNPP2,hnRNP-P2,FUS1,ALS6,TLS","biotype":"protein_coding","ncbi_id":"2521","summary":"This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6. [provided by RefSeq, Sep 2009]","start":31180110,"end":31194871,"strand":1,"description":"FUS RNA binding protein [Source:HGNC Symbol;Acc:HGNC:4010]"}, {"versioned_ensembl_gene_id":"ENSG00000233425.1","gene_symbol":"KRT18P67","gene_name":"keratin 18 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631239","summary":null,"start":122837557,"end":122838820,"strand":1,"description":"keratin 18 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48894]"}, {"versioned_ensembl_gene_id":"ENSG00000168852.12","gene_symbol":"TPTE2P5","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42356]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100616668","summary":null,"start":40822296,"end":40921749,"strand":-1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42356]"}, {"versioned_ensembl_gene_id":"ENSG00000106992.17","gene_symbol":"AK1","gene_name":"adenylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:361]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203","summary":"This gene encodes an adenylate kinase enzyme involved in energy metabolism and homeostasis of cellular adenine nucleotide ratios in different intracellular compartments. This gene is highly expressed in skeletal muscle, brain and erythrocytes. Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":127866480,"end":127877743,"strand":-1,"description":"adenylate kinase 1 [Source:HGNC Symbol;Acc:HGNC:361]"}, {"versioned_ensembl_gene_id":"ENSG00000226887.7","gene_symbol":"ERVMER34-1","gene_name":"endogenous retrovirus group MER34 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:42970]","synonyms":"envMER34","biotype":"protein_coding","ncbi_id":"100288413","summary":null,"start":52722618,"end":52751640,"strand":-1,"description":"endogenous retrovirus group MER34 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:42970]"}, {"versioned_ensembl_gene_id":"ENSG00000164363.9","gene_symbol":"SLC6A18","gene_name":"solute carrier family 6 member 18 [Source:HGNC Symbol;Acc:HGNC:26441]","synonyms":"Xtrp2,FLJ31236","biotype":"protein_coding","ncbi_id":"348932","summary":"The SLC6 family of proteins, which includes SLC6A18, act as specific transporters for neurotransmitters, amino acids, and osmolytes like betaine, taurine, and creatine. SLC6 proteins are sodium cotransporters that derive the energy for solute transport from the electrochemical gradient for sodium ions (Hoglund et al., 2005 [PubMed 16125675]).[supplied by OMIM, Apr 2010]","start":1225355,"end":1246189,"strand":1,"description":"solute carrier family 6 member 18 [Source:HGNC Symbol;Acc:HGNC:26441]"}, {"versioned_ensembl_gene_id":"ENSG00000249238.1","gene_symbol":"BCL9P1","gene_name":"B-cell CLL/lymphoma 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51328]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419324","summary":null,"start":67636382,"end":67638942,"strand":1,"description":"B-cell CLL/lymphoma 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51328]"}, {"versioned_ensembl_gene_id":"ENSG00000104043.14","gene_symbol":"ATP8B4","gene_name":"ATPase phospholipid transporting 8B4 (putative) [Source:HGNC Symbol;Acc:HGNC:13536]","synonyms":"KIAA1939,ATPIM","biotype":"protein_coding","ncbi_id":"79895","summary":"This gene encodes a member of the cation transport ATPase (P-type) family and type IV subfamily. The encoded protein is involved in phospholipid transport in the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":49858238,"end":50182817,"strand":-1,"description":"ATPase phospholipid transporting 8B4 (putative) [Source:HGNC Symbol;Acc:HGNC:13536]"}, {"versioned_ensembl_gene_id":"ENSG00000146090.15","gene_symbol":"RASGEF1C","gene_name":"RasGEF domain family member 1C [Source:HGNC Symbol;Acc:HGNC:27400]","synonyms":"FLJ35841","biotype":"protein_coding","ncbi_id":"255426","summary":null,"start":180100791,"end":180209153,"strand":-1,"description":"RasGEF domain family member 1C [Source:HGNC Symbol;Acc:HGNC:27400]"}, {"versioned_ensembl_gene_id":"ENSG00000254752.2","gene_symbol":"OR5M2P","gene_name":"olfactory receptor family 5 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14803]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79523","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56476287,"end":56484839,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14803]"}, {"versioned_ensembl_gene_id":"ENSG00000249364.5","gene_symbol":"AC112206.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67379378,"end":67805238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223769.3","gene_symbol":"CR388393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489201,"end":29489606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249767.1","gene_symbol":"ENPP7P10","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48693]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421805","summary":null,"start":9079023,"end":9141608,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48693]"}, {"versioned_ensembl_gene_id":"ENSG00000248877.2","gene_symbol":"PGBD4P4","gene_name":"piggyBac transposable element derived 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421146","summary":null,"start":130494673,"end":130495285,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44076]"}, {"versioned_ensembl_gene_id":"ENSG00000251326.1","gene_symbol":"LINC02479","gene_name":"long intergenic non-protein coding RNA 2479 [Source:HGNC Symbol;Acc:HGNC:53453]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377420","summary":null,"start":130376229,"end":130386371,"strand":1,"description":"long intergenic non-protein coding RNA 2479 [Source:HGNC Symbol;Acc:HGNC:53453]"}, {"versioned_ensembl_gene_id":"ENSG00000279311.1","gene_symbol":"AC092999.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":158869898,"end":158871821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167778.8","gene_symbol":"SPRYD3","gene_name":"SPRY domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25920]","synonyms":"FLJ14800","biotype":"protein_coding","ncbi_id":"84926","summary":null,"start":53064316,"end":53079420,"strand":-1,"description":"SPRY domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25920]"}, {"versioned_ensembl_gene_id":"ENSG00000250342.1","gene_symbol":"SNRPCP16","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480291","summary":null,"start":9051842,"end":9052051,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49831]"}, {"versioned_ensembl_gene_id":"ENSG00000278965.1","gene_symbol":"AC122713.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":180078357,"end":180081691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239870.1","gene_symbol":"AC112206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67608654,"end":67609130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242979.1","gene_symbol":"AC010285.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179933805,"end":179934196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278022.1","gene_symbol":"AC118658.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":98660210,"end":98660668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284636.1","gene_symbol":"AC073648.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9000841,"end":9001058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259475.1","gene_symbol":"AC036108.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98954149,"end":99105824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140006.11","gene_symbol":"WDR89","gene_name":"WD repeat domain 89 [Source:HGNC Symbol;Acc:HGNC:20489]","synonyms":"MGC9907,C14orf150","biotype":"protein_coding","ncbi_id":"112840","summary":null,"start":63597039,"end":63641861,"strand":-1,"description":"WD repeat domain 89 [Source:HGNC Symbol;Acc:HGNC:20489]"}, {"versioned_ensembl_gene_id":"ENSG00000166275.15","gene_symbol":"BORCS7","gene_name":"BLOC-1 related complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:23516]","synonyms":"FLJ40752,C10orf32","biotype":"protein_coding","ncbi_id":"119032","summary":null,"start":102854223,"end":102864961,"strand":1,"description":"BLOC-1 related complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:23516]"}, {"versioned_ensembl_gene_id":"ENSG00000136940.13","gene_symbol":"PDCL","gene_name":"phosducin like [Source:HGNC Symbol;Acc:HGNC:8770]","synonyms":"PhLP,DKFZp564M1863","biotype":"protein_coding","ncbi_id":"5082","summary":"Phosducin-like protein is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin, a phosphoprotein expressed in retina and pineal gland. Both phosducin-like protein and phosphoducin have been shown to regulate G-protein signaling by binding to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008]","start":122798389,"end":122828631,"strand":-1,"description":"phosducin like [Source:HGNC Symbol;Acc:HGNC:8770]"}, {"versioned_ensembl_gene_id":"ENSG00000169668.11","gene_symbol":"BCRP2","gene_name":"breakpoint cluster region pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1015]","synonyms":"BCR2,BCR-2,BCRL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400892","summary":null,"start":21103016,"end":21122285,"strand":1,"description":"breakpoint cluster region pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1015]"}, {"versioned_ensembl_gene_id":"ENSG00000282367.1","gene_symbol":"PTDSS2","gene_name":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]","synonyms":"PSS2","biotype":"protein_coding","ncbi_id":"81490","summary":"The protein encoded by this gene catalyzes the conversion of phosphatidylethanolamine to phosphatidylserine, a structural membrane phospholipid that functions in cell signaling, blood coagulation, and apoptosis. The encoded enzyme also has a high affinity for docosahexaenoic acid (DHA) and can use it to make DHA-containing phosphatidylserine. [provided by RefSeq, Jul 2016]","start":473895,"end":491399,"strand":1,"description":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]"}, {"versioned_ensembl_gene_id":"ENSG00000173334.3","gene_symbol":"TRIB1","gene_name":"tribbles pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:16891]","synonyms":"C8FW,TRB1,GIG2","biotype":"protein_coding","ncbi_id":"10221","summary":null,"start":125430321,"end":125438405,"strand":1,"description":"tribbles pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:16891]"}, {"versioned_ensembl_gene_id":"ENSG00000250405.2","gene_symbol":"AC113367.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130994253,"end":130996164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112078.13","gene_symbol":"KCTD20","gene_name":"potassium channel tetramerization domain containing 20 [Source:HGNC Symbol;Acc:HGNC:21052]","synonyms":"MGC14254,dJ108K11.3,C6orf69","biotype":"protein_coding","ncbi_id":"222658","summary":null,"start":36442767,"end":36491143,"strand":1,"description":"potassium channel tetramerization domain containing 20 [Source:HGNC Symbol;Acc:HGNC:21052]"}, {"versioned_ensembl_gene_id":"ENSG00000282669.1","gene_symbol":"AK3P2","gene_name":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]","synonyms":"HsT26053","biotype":"processed_pseudogene","ncbi_id":"100419074","summary":null,"start":143057059,"end":143057816,"strand":-1,"description":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]"}, {"versioned_ensembl_gene_id":"ENSG00000165202.3","gene_symbol":"OR1Q1","gene_name":"olfactory receptor family 1 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:8223]","synonyms":"OR1Q3,OR1Q2,HSTPCR106,TPCR106,OST226OR9-A,OST226,OR9-A","biotype":"protein_coding","ncbi_id":"158131","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122614738,"end":122615682,"strand":1,"description":"olfactory receptor family 1 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:8223]"}, {"versioned_ensembl_gene_id":"ENSG00000148814.17","gene_symbol":"LRRC27","gene_name":"leucine rich repeat containing 27 [Source:HGNC Symbol;Acc:HGNC:29346]","synonyms":"KIAA1674","biotype":"protein_coding","ncbi_id":"80313","summary":null,"start":132332154,"end":132379918,"strand":1,"description":"leucine rich repeat containing 27 [Source:HGNC Symbol;Acc:HGNC:29346]"}, {"versioned_ensembl_gene_id":"ENSG00000231919.1","gene_symbol":"BX908738.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215243,"end":29216186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231626.1","gene_symbol":"AC013402.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104580821,"end":104581890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136319.11","gene_symbol":"TTC5","gene_name":"tetratricopeptide repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:19274]","synonyms":"Strap","biotype":"protein_coding","ncbi_id":"91875","summary":null,"start":20256558,"end":20305994,"strand":-1,"description":"tetratricopeptide repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:19274]"}, {"versioned_ensembl_gene_id":"ENSG00000225441.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100915,"end":29101853,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000251195.1","gene_symbol":"AC105417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129177386,"end":129179094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259931.2","gene_symbol":"AC105036.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75512770,"end":75513040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162391.11","gene_symbol":"FAM151A","gene_name":"family with sequence similarity 151 member A [Source:HGNC Symbol;Acc:HGNC:25032]","synonyms":"MGC27169,C1orf179","biotype":"protein_coding","ncbi_id":"338094","summary":null,"start":54609182,"end":54623556,"strand":-1,"description":"family with sequence similarity 151 member A [Source:HGNC Symbol;Acc:HGNC:25032]"}, {"versioned_ensembl_gene_id":"ENSG00000261708.1","gene_symbol":"DNM1P32","gene_name":"dynamin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35179]","synonyms":"DNM1DN4@,DNM1DN4-5","biotype":"unprocessed_pseudogene","ncbi_id":"100132100","summary":null,"start":32436503,"end":32439767,"strand":1,"description":"dynamin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35179]"}, {"versioned_ensembl_gene_id":"ENSG00000248866.1","gene_symbol":"USP46-AS1","gene_name":"USP46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43991]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643783","summary":null,"start":52659406,"end":52661668,"strand":1,"description":"USP46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43991]"}, {"versioned_ensembl_gene_id":"ENSG00000154874.15","gene_symbol":"CCDC144B","gene_name":"coiled-coil domain containing 144B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26704]","synonyms":"FLJ36492","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284047","summary":null,"start":18537800,"end":18625617,"strand":-1,"description":"coiled-coil domain containing 144B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26704]"}, {"versioned_ensembl_gene_id":"ENSG00000227077.3","gene_symbol":"AC107983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18572752,"end":18572961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243925.1","gene_symbol":"AC091021.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26098839,"end":26099226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198369.9","gene_symbol":"SPRED2","gene_name":"sprouty related EVH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17722]","synonyms":"Spred-2,FLJ31917,FLJ21897","biotype":"protein_coding","ncbi_id":"200734","summary":"SPRED2 is a member of the Sprouty (see SPRY1; MIM 602465)/SPRED family of proteins that regulate growth factor-induced activation of the MAP kinase cascade (see MAPK1; MIM 176948) (Nonami et al., 2004 [PubMed 15465815]).[supplied by OMIM, Mar 2008]","start":65310851,"end":65432637,"strand":-1,"description":"sprouty related EVH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17722]"}, {"versioned_ensembl_gene_id":"ENSG00000212717.3","gene_symbol":"DEFB117","gene_name":"defensin beta 117 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18098]","synonyms":"DEFB-17","biotype":"processed_pseudogene","ncbi_id":"245931","summary":null,"start":31360790,"end":31360930,"strand":1,"description":"defensin beta 117 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18098]"}, {"versioned_ensembl_gene_id":"ENSG00000277881.1","gene_symbol":"AL645927.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29450210,"end":29450558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000054965.10","gene_symbol":"FAM168A","gene_name":"family with sequence similarity 168 member A [Source:HGNC Symbol;Acc:HGNC:28999]","synonyms":"TCRP1,KIAA0280","biotype":"protein_coding","ncbi_id":"23201","summary":null,"start":73400487,"end":73598189,"strand":-1,"description":"family with sequence similarity 168 member A [Source:HGNC Symbol;Acc:HGNC:28999]"}, {"versioned_ensembl_gene_id":"ENSG00000256148.1","gene_symbol":"AP000763.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73510658,"end":73510820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130592.15","gene_symbol":"LSP1","gene_name":"lymphocyte-specific protein 1 [Source:HGNC Symbol;Acc:HGNC:6707]","synonyms":"WP34","biotype":"protein_coding","ncbi_id":"4046","summary":"This gene encodes an intracellular F-actin binding protein. The protein is expressed in lymphocytes, neutrophils, macrophages, and endothelium and may regulate neutrophil motility, adhesion to fibrinogen matrix proteins, and transendothelial migration. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":1852970,"end":1892267,"strand":1,"description":"lymphocyte-specific protein 1 [Source:HGNC Symbol;Acc:HGNC:6707]"}, {"versioned_ensembl_gene_id":"ENSG00000254619.1","gene_symbol":"AC113192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33810145,"end":33811178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255169.1","gene_symbol":"AC113192.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33804768,"end":33805641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254102.1","gene_symbol":"AC090136.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64574306,"end":64581888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255161.1","gene_symbol":"AC113192.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33787054,"end":33787795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255272.1","gene_symbol":"AC113192.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33776188,"end":33779495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262011.1","gene_symbol":"AC003009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13331368,"end":13332583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130159.13","gene_symbol":"ECSIT","gene_name":"ECSIT signalling integrator [Source:HGNC Symbol;Acc:HGNC:29548]","synonyms":"SITPEC","biotype":"protein_coding","ncbi_id":"51295","summary":null,"start":11505916,"end":11529174,"strand":-1,"description":"ECSIT signalling integrator [Source:HGNC Symbol;Acc:HGNC:29548]"}, {"versioned_ensembl_gene_id":"ENSG00000180316.12","gene_symbol":"PNPLA1","gene_name":"patatin like phospholipase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21246]","synonyms":"FLJ38755,dJ50J22.1","biotype":"protein_coding","ncbi_id":"285848","summary":"The protein encoded by this gene belongs to the patatin-like phospholipase (PNPLA) family, which is characterized by the presence of a highly conserved patatin domain. PNPLA family members have diverse lipolytic and acyltransferase activities, and are key elements in lipid metabolism. While other members of this family have been well characterized, the function of this gene remained an enigma. However, recent studies show that this gene is expressed in the skin epidermal keratinocytes, and has a role in glycerophospholipid metabolism in the cutaneous barrier. Consistent with these observations, mutations in this gene are associated with ichthyosis in human (autosomal recessive congenital ichthyoses, ARCI) and dog. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":36243203,"end":36312229,"strand":1,"description":"patatin like phospholipase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21246]"}, {"versioned_ensembl_gene_id":"ENSG00000279083.1","gene_symbol":"AL160274.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35360540,"end":35362054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130811.11","gene_symbol":"EIF3G","gene_name":"eukaryotic translation initiation factor 3 subunit G [Source:HGNC Symbol;Acc:HGNC:3274]","synonyms":"EIF3S4,eIF3g,eIF3-p44,eIF3-delta","biotype":"protein_coding","ncbi_id":"8666","summary":"This gene encodes a core subunit of the eukaryotic translation initiation factor 3 (eIF3) complex, which is required for initiation of protein translation. An N-terminal caspase cleavage product of the encoded protein may stimulate degradation of DNA. A mutation in this gene is associated with narcolepsy. [provided by RefSeq, Jul 2016]","start":10115017,"end":10119918,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit G [Source:HGNC Symbol;Acc:HGNC:3274]"}, {"versioned_ensembl_gene_id":"ENSG00000232383.1","gene_symbol":"AC010677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26276195,"end":26276606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237462.10","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RNF76,RFP","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28914742,"end":28923955,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000273200.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859590,"end":28863315,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000226979.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31572054,"end":31574324,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000262651.1","gene_symbol":"AL513043.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63612761,"end":63612903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235812.4","gene_symbol":"ADAM21P1","gene_name":"ADAM metallopeptidase domain 21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19822]","synonyms":"ADAM21P","biotype":"transcribed_processed_pseudogene","ncbi_id":"145241","summary":null,"start":70245491,"end":70247801,"strand":-1,"description":"ADAM metallopeptidase domain 21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19822]"}, {"versioned_ensembl_gene_id":"ENSG00000223708.1","gene_symbol":"AL645935.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29931616,"end":29932608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255063.1","gene_symbol":"AP001646.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82805354,"end":82806509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215246.5","gene_symbol":"AC116351.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":987180,"end":997308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267359.1","gene_symbol":"AC015911.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35553205,"end":35554767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230172.1","gene_symbol":"AC090957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14764952,"end":14767440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079277.19","gene_symbol":"MKNK1","gene_name":"MAP kinase interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:7110]","synonyms":"MNK1","biotype":"protein_coding","ncbi_id":"8569","summary":"This gene encodes a Ser/Thr protein kinase that interacts with, and is activated by ERK1 and p38 mitogen-activated protein kinases, and thus may play a role in the response to environmental stress and cytokines. This kinase may also regulate transcription by phosphorylating eIF4E via interaction with the C-terminal region of eIF4G. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2012]","start":46557408,"end":46616843,"strand":-1,"description":"MAP kinase interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:7110]"}, {"versioned_ensembl_gene_id":"ENSG00000132254.12","gene_symbol":"ARFIP2","gene_name":"ADP ribosylation factor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17160]","synonyms":"POR1","biotype":"protein_coding","ncbi_id":"23647","summary":null,"start":6474683,"end":6481479,"strand":-1,"description":"ADP ribosylation factor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17160]"}, {"versioned_ensembl_gene_id":"ENSG00000177776.8","gene_symbol":"AC005519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74377818,"end":74378418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269956.1","gene_symbol":"MKNK1-AS1","gene_name":"MKNK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44129]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507423","summary":null,"start":46538696,"end":46570255,"strand":1,"description":"MKNK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44129]"}, {"versioned_ensembl_gene_id":"ENSG00000248647.2","gene_symbol":"AC012613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149163955,"end":149276776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276110.1","gene_symbol":"AC242988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150255095,"end":150257286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213262.3","gene_symbol":"VDAC2P3","gene_name":"voltage dependent anion channel 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401959","summary":null,"start":117640812,"end":117641639,"strand":-1,"description":"voltage dependent anion channel 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51931]"}, {"versioned_ensembl_gene_id":"ENSG00000249494.5","gene_symbol":"AC008629.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119006347,"end":119070890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229995.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"352967","summary":null,"start":29806254,"end":29806385,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000224253.1","gene_symbol":"AL669813.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29742254,"end":29742478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237395.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29960309,"end":29961971,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000274105.1","gene_symbol":"AC084824.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32728169,"end":32729024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170426.1","gene_symbol":"SDR9C7","gene_name":"short chain dehydrogenase/reductase family 9C member 7 [Source:HGNC Symbol;Acc:HGNC:29958]","synonyms":"SDR-O,RDHS","biotype":"protein_coding","ncbi_id":"121214","summary":"This gene encodes a protein with similarity to the short-chain dehydrogenase/reductase (SDR) family but has not been shown to have retinoid or dehydrogenase activities. [provided by RefSeq, Apr 2010]","start":56923154,"end":56934405,"strand":-1,"description":"short chain dehydrogenase/reductase family 9C member 7 [Source:HGNC Symbol;Acc:HGNC:29958]"}, {"versioned_ensembl_gene_id":"ENSG00000226755.2","gene_symbol":"VPS25P1","gene_name":"VPS25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44250]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441899","summary":null,"start":117549415,"end":117549922,"strand":1,"description":"VPS25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44250]"}, {"versioned_ensembl_gene_id":"ENSG00000269296.1","gene_symbol":"AC005614.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40090754,"end":40094406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260293.2","gene_symbol":"AC106820.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2476558,"end":2482173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273326.1","gene_symbol":"TAS2R7","gene_name":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]","synonyms":"TRB4,T2R7","biotype":"protein_coding","ncbi_id":"50837","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10801532,"end":10802627,"strand":-1,"description":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]"}, {"versioned_ensembl_gene_id":"ENSG00000238022.1","gene_symbol":"AL390730.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165215980,"end":165219104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225032.5","gene_symbol":"AL162586.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127816066,"end":127822520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219992.2","gene_symbol":"AL391422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3754099,"end":3754840,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261532.1","gene_symbol":"AC009065.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2211997,"end":2212863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259320.1","gene_symbol":"AC022523.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98122563,"end":98131607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259199.1","gene_symbol":"AC022523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98046667,"end":98293177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206291.10","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":32993608,"end":33009820,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000203618.5","gene_symbol":"GP1BB","gene_name":"glycoprotein Ib platelet beta subunit [Source:HGNC Symbol;Acc:HGNC:4440]","synonyms":"GPIbbeta,CD42c","biotype":"protein_coding","ncbi_id":"2812","summary":"Platelet glycoprotein Ib (GPIb) is a heterodimeric transmembrane protein consisting of a disulfide-linked 140 kD alpha chain and 22 kD beta chain. It is part of the GPIb-V-IX system that constitutes the receptor for von Willebrand factor (VWF), and mediates platelet adhesion in the arterial circulation. GPIb alpha chain provides the VWF binding site, and GPIb beta contributes to surface expression of the receptor and participates in transmembrane signaling through phosphorylation of its intracellular domain. Mutations in the GPIb beta subunit have been associated with Bernard-Soulier syndrome, velocardiofacial syndrome and giant platelet disorder. The 206 amino acid precursor of GPIb beta is synthesized from a 1.0 kb mRNA expressed in plateletes and megakaryocytes. A 411 amino acid protein arising from a longer, unspliced transcript in endothelial cells has been described; however, the authenticity of this product has been questioned. Yet another less abundant GPIb beta mRNA species of 3.5 kb, expressed in nonhematopoietic tissues such as endothelium, brain and heart, was shown to result from inefficient usage of a non-consensus polyA signal in the neighboring upstream gene (SEPT5, septin 5). In the absence of polyadenylation from its own imperfect site, the SEPT5 gene produces read-through transcripts that use the consensus polyA signal of this gene. [provided by RefSeq, Dec 2010]","start":19722945,"end":19724771,"strand":1,"description":"glycoprotein Ib platelet beta subunit [Source:HGNC Symbol;Acc:HGNC:4440]"}, {"versioned_ensembl_gene_id":"ENSG00000249547.1","gene_symbol":"AC092440.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23234625,"end":23285573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279642.1","gene_symbol":"AL023973.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44486295,"end":44486914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196312.12","gene_symbol":"MFSD14C","gene_name":"major facilitator superfamily domain containing 14C [Source:HGNC Symbol;Acc:HGNC:23672]","synonyms":"MGC12945,HIATL2","biotype":"protein_coding","ncbi_id":"84278","summary":null,"start":96897917,"end":97013708,"strand":-1,"description":"major facilitator superfamily domain containing 14C [Source:HGNC Symbol;Acc:HGNC:23672]"}, {"versioned_ensembl_gene_id":"ENSG00000233519.1","gene_symbol":"AL590490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240400671,"end":240401123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186124.4","gene_symbol":"OR9M1P","gene_name":"olfactory receptor family 9 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15327]","synonyms":"OR5BG1P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81153","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55850347,"end":55858547,"strand":1,"description":"olfactory receptor family 9 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15327]"}, {"versioned_ensembl_gene_id":"ENSG00000256966.6","gene_symbol":"AL513165.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37512547,"end":37592469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234123.1","gene_symbol":"RHBDF1P1","gene_name":"RHBDF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44499]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"131973","summary":null,"start":14572852,"end":14574792,"strand":-1,"description":"RHBDF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44499]"}, {"versioned_ensembl_gene_id":"ENSG00000279240.1","gene_symbol":"AC063980.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136376348,"end":136397042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260991.2","gene_symbol":"AC120498.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1280161,"end":1280544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231755.1","gene_symbol":"CHODL-AS1","gene_name":"CHODL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1279]","synonyms":"NCRNA00157,C21orf39","biotype":"lincRNA","ncbi_id":"54075","summary":null,"start":17835016,"end":17885608,"strand":-1,"description":"CHODL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1279]"}, {"versioned_ensembl_gene_id":"ENSG00000254457.2","gene_symbol":"OR5D2P","gene_name":"olfactory receptor family 5 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8335]","synonyms":"OR11-7a,OR8-125,OR5D9P,OR5D8P,OR5D7P,OR5D6P,OR5D5P,OR5D1P,OR5D12P,OR5D12,OR5D11P,OR5D11,OR5D10P,R5D9P,OR18-44,OR912-94,OR18-43,OR912-91,OR18-42,OR912-47,OR18-17,OR8-127","biotype":"unprocessed_pseudogene","ncbi_id":"8595","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55714799,"end":55715709,"strand":1,"description":"olfactory receptor family 5 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8335]"}, {"versioned_ensembl_gene_id":"ENSG00000279704.1","gene_symbol":"AC148477.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132351855,"end":132352322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126264.9","gene_symbol":"HCST","gene_name":"hematopoietic cell signal transducer [Source:HGNC Symbol;Acc:HGNC:16977]","synonyms":"DAP10,PIK3AP,KAP10,DKFZP586C1522","biotype":"protein_coding","ncbi_id":"10870","summary":"This gene encodes a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part of the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. As part of this receptor complex, this protein may activate phosphatidylinositol 3-kinase dependent signaling pathways through its intracytoplasmic YxxM motif. This receptor complex may have a role in cell survival and proliferation by activation of NK and T cell responses. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":35902480,"end":35904377,"strand":1,"description":"hematopoietic cell signal transducer [Source:HGNC Symbol;Acc:HGNC:16977]"}, {"versioned_ensembl_gene_id":"ENSG00000188385.11","gene_symbol":"JAKMIP3","gene_name":"Janus kinase and microtubule interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23523]","synonyms":"NECC2,KIAA4091,FLJ37857,C10orf39,C10orf14,bA140A10.5","biotype":"protein_coding","ncbi_id":"282973","summary":null,"start":132104671,"end":132184809,"strand":1,"description":"Janus kinase and microtubule interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23523]"}, {"versioned_ensembl_gene_id":"ENSG00000244327.1","gene_symbol":"AC109992.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":142465315,"end":142472337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230266.1","gene_symbol":"XXYLT1-AS2","gene_name":"XXYLT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41154]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410543","summary":null,"start":195147871,"end":195152790,"strand":1,"description":"XXYLT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41154]"}, {"versioned_ensembl_gene_id":"ENSG00000218713.1","gene_symbol":"AL512378.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53206598,"end":53208697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224083.1","gene_symbol":"MTCO1P11","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52013]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075264","summary":null,"start":5096666,"end":5098193,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52013]"}, {"versioned_ensembl_gene_id":"ENSG00000267711.1","gene_symbol":"AC060766.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35400878,"end":35403006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267315.1","gene_symbol":"AC060766.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35377416,"end":35377678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159640.15","gene_symbol":"ACE","gene_name":"angiotensin I converting enzyme [Source:HGNC Symbol;Acc:HGNC:2707]","synonyms":"DCP1,CD143,ACE1","biotype":"protein_coding","ncbi_id":"1636","summary":"This gene encodes an enzyme involved in blood pressure regulation and electrolyte balance. It catalyzes the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance. This angiotensin converting enzyme (ACE) also inactivates the vasodilator protein, bradykinin. Accordingly, the encoded enzyme increases blood pressure and is a drug target of ACE inhibitors, which are often prescribed to reduce blood pressure. This enzyme additionally plays a role in fertility through its ability to cleave and release GPI-anchored membrane proteins in spermatozoa. Many studies have associated the presence or absence of a 287 bp Alu repeat element in this gene with the levels of circulating enzyme. This polymorphism, as well as mutations in this gene, have been implicated in a wide variety of diseases including cardiovascular pathophysiologies, psoriasis, renal disease, stroke, and Alzheimer's disease. Regulation of the homologous ACE2 gene may be involved in progression of disease caused by several human coronaviruses, including SARS-CoV and SARS-CoV-2. Alternative splicing results in multiple transcript variants encoding both somatic (sACE) and male-specific testicular (tACE) isoforms. [provided by RefSeq, Sep 2020]","start":63477061,"end":63498380,"strand":1,"description":"angiotensin I converting enzyme [Source:HGNC Symbol;Acc:HGNC:2707]"}, {"versioned_ensembl_gene_id":"ENSG00000128699.13","gene_symbol":"ORMDL1","gene_name":"ORMDL sphingolipid biosynthesis regulator 1 [Source:HGNC Symbol;Acc:HGNC:16036]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94101","summary":null,"start":189770323,"end":189784371,"strand":-1,"description":"ORMDL sphingolipid biosynthesis regulator 1 [Source:HGNC Symbol;Acc:HGNC:16036]"}, {"versioned_ensembl_gene_id":"ENSG00000109189.12","gene_symbol":"USP46","gene_name":"ubiquitin specific peptidase 46 [Source:HGNC Symbol;Acc:HGNC:20075]","synonyms":"FLJ12552","biotype":"protein_coding","ncbi_id":"64854","summary":"Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP46 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Jun 2009]","start":52590972,"end":52659335,"strand":-1,"description":"ubiquitin specific peptidase 46 [Source:HGNC Symbol;Acc:HGNC:20075]"}, {"versioned_ensembl_gene_id":"ENSG00000228979.4","gene_symbol":"AC113554.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63471604,"end":63472093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237281.1","gene_symbol":"CATIP-AS2","gene_name":"CATIP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41079]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103689911","summary":null,"start":218326889,"end":218357966,"strand":-1,"description":"CATIP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41079]"}, {"versioned_ensembl_gene_id":"ENSG00000270673.1","gene_symbol":"YTHDF3-AS1","gene_name":"YTHDF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48728]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101410533","summary":null,"start":63167725,"end":63168442,"strand":-1,"description":"YTHDF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48728]"}, {"versioned_ensembl_gene_id":"ENSG00000158560.14","gene_symbol":"DYNC1I1","gene_name":"dynein cytoplasmic 1 intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2963]","synonyms":"DNCIC1,DNCI1","biotype":"protein_coding","ncbi_id":"1780","summary":null,"start":95772506,"end":96110322,"strand":1,"description":"dynein cytoplasmic 1 intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2963]"}, {"versioned_ensembl_gene_id":"ENSG00000266718.1","gene_symbol":"AC079336.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32495536,"end":32499333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105483.17","gene_symbol":"CARD8","gene_name":"caspase recruitment domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17057]","synonyms":"CARDINAL,TUCAN,NDPP,KIAA0955,Dakar","biotype":"protein_coding","ncbi_id":"22900","summary":"The protein encoded by this gene belongs to the caspase recruitment domain (CARD)-containing family of proteins, which are involved in pathways leading to activation of caspases or nuclear factor kappa-B (NFKB). This protein may be a component of the inflammasome, a protein complex that plays a role in the activation of proinflammatory caspases. It is thought that this protein acts as an adaptor molecule that negatively regulates NFKB activation, CASP1-dependent IL1B secretion, and apoptosis. Polymorphisms in this gene may be associated with a susceptibility to rheumatoid arthritis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]","start":48180770,"end":48255946,"strand":-1,"description":"caspase recruitment domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17057]"}, {"versioned_ensembl_gene_id":"ENSG00000228245.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31533053,"end":31533887,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000227632.2","gene_symbol":"AC018804.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130202312,"end":130212628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248351.1","gene_symbol":"HSPD1P18","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35136]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100359397","summary":null,"start":136381268,"end":136381511,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35136]"}, {"versioned_ensembl_gene_id":"ENSG00000226758.1","gene_symbol":"DISC1-IT1","gene_name":"DISC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41325]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"104472714","summary":null,"start":231925834,"end":231945233,"strand":1,"description":"DISC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41325]"}, {"versioned_ensembl_gene_id":"ENSG00000179840.5","gene_symbol":"PIK3CD-AS1","gene_name":"PIK3CD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32346]","synonyms":"C1orf200","biotype":"antisense_RNA","ncbi_id":"644997","summary":null,"start":9652610,"end":9654586,"strand":-1,"description":"PIK3CD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32346]"}, {"versioned_ensembl_gene_id":"ENSG00000107815.7","gene_symbol":"TWNK","gene_name":"twinkle mtDNA helicase [Source:HGNC Symbol;Acc:HGNC:1160]","synonyms":"TWINL,TWINKLE,PEO1,PEO,IOSCA,FLJ21832,C10orf2","biotype":"protein_coding","ncbi_id":"56652","summary":"This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009]","start":100987367,"end":100994401,"strand":1,"description":"twinkle mtDNA helicase [Source:HGNC Symbol;Acc:HGNC:1160]"}, {"versioned_ensembl_gene_id":"ENSG00000224070.1","gene_symbol":"HMGN1P6","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874430","summary":null,"start":206259628,"end":206259918,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]"}, {"versioned_ensembl_gene_id":"ENSG00000104892.16","gene_symbol":"KLC3","gene_name":"kinesin light chain 3 [Source:HGNC Symbol;Acc:HGNC:20717]","synonyms":"KNS2B,KLCt,KLC2L","biotype":"protein_coding","ncbi_id":"147700","summary":"This gene encodes a member of the kinesin light chain gene family. Kinesins are molecular motors involved in the transport of cargo along microtubules, and are composed of two kinesin heavy chain (KHC) and two kinesin light chain (KLC) molecules. KLCs are thought to typically be involved in binding cargo and regulating kinesin activity. In the rat, a protein similar to this gene product is expressed in post-meiotic spermatids, where it associates with structural components of sperm tails and mitochondria. [provided by RefSeq, Jul 2008]","start":45333434,"end":45351520,"strand":1,"description":"kinesin light chain 3 [Source:HGNC Symbol;Acc:HGNC:20717]"}, {"versioned_ensembl_gene_id":"ENSG00000155269.11","gene_symbol":"GPR78","gene_name":"G protein-coupled receptor 78 [Source:HGNC Symbol;Acc:HGNC:4528]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27201","summary":"The protein encoded by this gene belongs to the G protein-coupled receptor family, which contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. This is an orphan receptor, which displays significant level of constitutive activity. Association analysis shows preliminary evidence for the involvement of this gene in susceptibility to bipolar affective disorder and schizophrenia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2011]","start":8558725,"end":8619761,"strand":1,"description":"G protein-coupled receptor 78 [Source:HGNC Symbol;Acc:HGNC:4528]"}, {"versioned_ensembl_gene_id":"ENSG00000176658.16","gene_symbol":"MYO1D","gene_name":"myosin ID [Source:HGNC Symbol;Acc:HGNC:7598]","synonyms":"PPP1R108,myr4,KIAA0727","biotype":"protein_coding","ncbi_id":"4642","summary":null,"start":32492522,"end":32877177,"strand":-1,"description":"myosin ID [Source:HGNC Symbol;Acc:HGNC:7598]"}, {"versioned_ensembl_gene_id":"ENSG00000281379.2","gene_symbol":"SEPT14P19","gene_name":"septin 14 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51707]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107105271","summary":null,"start":186373,"end":195696,"strand":-1,"description":"septin 14 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51707]"}, {"versioned_ensembl_gene_id":"ENSG00000235683.1","gene_symbol":"AC018442.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99695957,"end":99698017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268222.1","gene_symbol":"EEF1A1P7","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3202]","synonyms":"EEF1AL5","biotype":"processed_pseudogene","ncbi_id":"390924","summary":null,"start":35382172,"end":35384052,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3202]"}, {"versioned_ensembl_gene_id":"ENSG00000276993.1","gene_symbol":"AC116003.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75387056,"end":75387596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232332.1","gene_symbol":"AC233982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76029895,"end":76030330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231924.9","gene_symbol":"PSG1","gene_name":"pregnancy specific beta-1-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:9514]","synonyms":"PBG1,CD66f,PSGGA,PSBG1","biotype":"protein_coding","ncbi_id":"5669","summary":"The human placenta is a multihormonal endocrine organ that produces hormones, enzymes, and other molecules that support fetal survival and development. Pregnancy-specific beta-1-glycoprotein (PSBG, PSG) is a major product of the syncytiotrophoblast, reaching concentrations of 100 to 290 mg/l at term in the serum of pregnant women (Horne et al., 1976 [PubMed 971765]). PSG is a member of the immunoglobulin (Ig) superfamily (Watanabe and Chou, 1988 [PubMed 3257488]; Streydio et al., 1988 [PubMed 3260773]).[supplied by OMIM, Oct 2009]","start":42866464,"end":42879822,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:9514]"}, {"versioned_ensembl_gene_id":"ENSG00000223753.2","gene_symbol":"AC234775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101683780,"end":101684449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267641.1","gene_symbol":"BNIP3P16","gene_name":"BCL2 interacting protein 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480418","summary":null,"start":20175013,"end":20177063,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49696]"}, {"versioned_ensembl_gene_id":"ENSG00000272848.1","gene_symbol":"AL009176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169426420,"end":169427069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236778.7","gene_symbol":"INTS6-AS1","gene_name":"INTS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42691]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507398","summary":null,"start":51452367,"end":51552364,"strand":1,"description":"INTS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42691]"}, {"versioned_ensembl_gene_id":"ENSG00000255345.1","gene_symbol":"AP002957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79092848,"end":79098003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095917.13","gene_symbol":"TPSD1","gene_name":"tryptase delta 1 [Source:HGNC Symbol;Acc:HGNC:14118]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23430","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. Although this gene may be an exception, most of the tryptase genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. This gene was once considered to be a pseudogene, although it is now believed to be a functional gene that encodes a protein. [provided by RefSeq, Jul 2008]","start":1256059,"end":1258998,"strand":1,"description":"tryptase delta 1 [Source:HGNC Symbol;Acc:HGNC:14118]"}, {"versioned_ensembl_gene_id":"ENSG00000260182.1","gene_symbol":"AC120498.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1257339,"end":1258074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234572.1","gene_symbol":"LINC01800","gene_name":"long intergenic non-protein coding RNA 1800 [Source:HGNC Symbol;Acc:HGNC:52590]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927438","summary":null,"start":64846130,"end":64863626,"strand":-1,"description":"long intergenic non-protein coding RNA 1800 [Source:HGNC Symbol;Acc:HGNC:52590]"}, {"versioned_ensembl_gene_id":"ENSG00000231697.3","gene_symbol":"NANOGP5","gene_name":"Nanog homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23103]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"414133","summary":null,"start":100175178,"end":100176054,"strand":1,"description":"Nanog homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23103]"}, {"versioned_ensembl_gene_id":"ENSG00000216687.2","gene_symbol":"AL390237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58071720,"end":58073134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226794.1","gene_symbol":"MTND1P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873339","summary":null,"start":69595487,"end":69596436,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42069]"}, {"versioned_ensembl_gene_id":"ENSG00000229659.1","gene_symbol":"RPL26P6","gene_name":"ribosomal protein L26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131526","summary":null,"start":73422259,"end":73422696,"strand":-1,"description":"ribosomal protein L26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34023]"}, {"versioned_ensembl_gene_id":"ENSG00000253297.1","gene_symbol":"AC008627.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":148644687,"end":148646390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254686.2","gene_symbol":"AL138812.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35656694,"end":35661339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128656.13","gene_symbol":"CHN1","gene_name":"chimerin 1 [Source:HGNC Symbol;Acc:HGNC:1943]","synonyms":"CHN,ARHGAP2,RhoGAP2,n-chimerin,DURS2","biotype":"protein_coding","ncbi_id":"1123","summary":"This gene encodes GTPase-activating protein for ras-related p21-rac and a phorbol ester receptor. It is predominantly expressed in neurons, and plays an important role in neuronal signal-transduction mechanisms. Mutations in this gene are associated with Duane's retraction syndrome 2 (DURS2). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]","start":174799363,"end":175005369,"strand":-1,"description":"chimerin 1 [Source:HGNC Symbol;Acc:HGNC:1943]"}, {"versioned_ensembl_gene_id":"ENSG00000166343.9","gene_symbol":"MSS51","gene_name":"MSS51 mitochondrial translational activator [Source:HGNC Symbol;Acc:HGNC:21000]","synonyms":"ZMYND17,FLJ39565","biotype":"protein_coding","ncbi_id":"118490","summary":null,"start":73423579,"end":73433561,"strand":-1,"description":"MSS51 mitochondrial translational activator [Source:HGNC Symbol;Acc:HGNC:21000]"}, {"versioned_ensembl_gene_id":"ENSG00000117450.13","gene_symbol":"PRDX1","gene_name":"peroxiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:9352]","synonyms":"PAGA,NKEFA","biotype":"protein_coding","ncbi_id":"5052","summary":"This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of CD8(+) T-cells. This protein may have a proliferative effect and play a role in cancer development or progression. Four transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jan 2011]","start":45511036,"end":45523047,"strand":-1,"description":"peroxiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:9352]"}, {"versioned_ensembl_gene_id":"ENSG00000235294.1","gene_symbol":"RPL7AP25","gene_name":"ribosomal protein L7a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271042","summary":null,"start":181505075,"end":181505879,"strand":-1,"description":"ribosomal protein L7a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36714]"}, {"versioned_ensembl_gene_id":"ENSG00000171224.8","gene_symbol":"C10orf35","gene_name":"chromosome 10 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:23519]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219738","summary":null,"start":69630251,"end":69633599,"strand":1,"description":"chromosome 10 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:23519]"}, {"versioned_ensembl_gene_id":"ENSG00000237806.1","gene_symbol":"FAUP2","gene_name":"FAU, ubiquitin like and ribosomal protein S30 fusion pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36535]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271125","summary":null,"start":181242345,"end":181242901,"strand":-1,"description":"FAU, ubiquitin like and ribosomal protein S30 fusion pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36535]"}, {"versioned_ensembl_gene_id":"ENSG00000185897.6","gene_symbol":"FFAR3","gene_name":"free fatty acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:4499]","synonyms":"GPR41,FFA3R","biotype":"protein_coding","ncbi_id":"2865","summary":null,"start":35358460,"end":35360485,"strand":1,"description":"free fatty acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:4499]"}, {"versioned_ensembl_gene_id":"ENSG00000251261.4","gene_symbol":"OR7H2P","gene_name":"olfactory receptor family 7 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31314]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403301","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101816475,"end":101816780,"strand":-1,"description":"olfactory receptor family 7 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31314]"}, {"versioned_ensembl_gene_id":"ENSG00000150907.7","gene_symbol":"FOXO1","gene_name":"forkhead box O1 [Source:HGNC Symbol;Acc:HGNC:3819]","synonyms":"FOXO1A,FKHR,FKH1","biotype":"protein_coding","ncbi_id":"2308","summary":"This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma. [provided by RefSeq, Jul 2008]","start":40469953,"end":40666597,"strand":-1,"description":"forkhead box O1 [Source:HGNC Symbol;Acc:HGNC:3819]"}, {"versioned_ensembl_gene_id":"ENSG00000241231.1","gene_symbol":"AC022294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181421058,"end":181442486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267364.1","gene_symbol":"AC022706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35313502,"end":35324900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230570.1","gene_symbol":"AL139095.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7340854,"end":7342056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249495.1","gene_symbol":"AC117525.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101976296,"end":101976798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242808.7","gene_symbol":"SOX2-OT","gene_name":"SOX2 overlapping transcript [Source:HGNC Symbol;Acc:HGNC:20209]","synonyms":"SOX2OT,NCRNA00043,DKFZp761J1324","biotype":"sense_overlapping","ncbi_id":"347689","summary":"This gene produces alternatively spliced long non-coding RNAs. These RNAs were observed to be upregulated in tumor cells and positively correlated to expression of the SRY-box 2 gene. Overexpression of these transcripts may promote cell proliferation. [provided by RefSeq, Dec 2017]","start":180989770,"end":181836880,"strand":1,"description":"SOX2 overlapping transcript [Source:HGNC Symbol;Acc:HGNC:20209]"}, {"versioned_ensembl_gene_id":"ENSG00000267271.1","gene_symbol":"AC060766.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35344231,"end":35344564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166326.6","gene_symbol":"TRIM44","gene_name":"tripartite motif containing 44 [Source:HGNC Symbol;Acc:HGNC:19016]","synonyms":"MC7,DIPB","biotype":"protein_coding","ncbi_id":"54765","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, namely a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]","start":35662805,"end":35818007,"strand":1,"description":"tripartite motif containing 44 [Source:HGNC Symbol;Acc:HGNC:19016]"}, {"versioned_ensembl_gene_id":"ENSG00000169040.14","gene_symbol":"PMCHL2","gene_name":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5370","summary":null,"start":71375786,"end":71385993,"strand":1,"description":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]"}, {"versioned_ensembl_gene_id":"ENSG00000206190.11","gene_symbol":"ATP10A","gene_name":"ATPase phospholipid transporting 10A (putative) [Source:HGNC Symbol;Acc:HGNC:13542]","synonyms":"KIAA0566,ATPVC,ATPVA,ATP10C","biotype":"protein_coding","ncbi_id":"57194","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'. [provided by RefSeq, Jul 2008]","start":25677273,"end":25865172,"strand":-1,"description":"ATPase phospholipid transporting 10A (putative) [Source:HGNC Symbol;Acc:HGNC:13542]"}, {"versioned_ensembl_gene_id":"ENSG00000110046.12","gene_symbol":"ATG2A","gene_name":"autophagy related 2A [Source:HGNC Symbol;Acc:HGNC:29028]","synonyms":"KIAA0404","biotype":"protein_coding","ncbi_id":"23130","summary":null,"start":64894546,"end":64917248,"strand":-1,"description":"autophagy related 2A [Source:HGNC Symbol;Acc:HGNC:29028]"}, {"versioned_ensembl_gene_id":"ENSG00000164074.14","gene_symbol":"ABHD18","gene_name":"abhydrolase domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26111]","synonyms":"FLJ21106,C4orf29","biotype":"protein_coding","ncbi_id":"80167","summary":null,"start":127965306,"end":128039711,"strand":1,"description":"abhydrolase domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26111]"}, {"versioned_ensembl_gene_id":"ENSG00000230710.1","gene_symbol":"LINC00332","gene_name":"long intergenic non-protein coding RNA 332 [Source:HGNC Symbol;Acc:HGNC:42049]","synonyms":"NCRNA00332","biotype":"lincRNA","ncbi_id":"100874127","summary":null,"start":40181809,"end":40189028,"strand":1,"description":"long intergenic non-protein coding RNA 332 [Source:HGNC Symbol;Acc:HGNC:42049]"}, {"versioned_ensembl_gene_id":"ENSG00000165410.14","gene_symbol":"CFL2","gene_name":"cofilin 2 [Source:HGNC Symbol;Acc:HGNC:1875]","synonyms":"NEM7","biotype":"protein_coding","ncbi_id":"1073","summary":"This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH-dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":34706769,"end":34714823,"strand":-1,"description":"cofilin 2 [Source:HGNC Symbol;Acc:HGNC:1875]"}, {"versioned_ensembl_gene_id":"ENSG00000229456.1","gene_symbol":"RLIMP1","gene_name":"ring finger protein, LIM domain interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39682]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533695","summary":null,"start":40618738,"end":40621348,"strand":1,"description":"ring finger protein, LIM domain interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39682]"}, {"versioned_ensembl_gene_id":"ENSG00000227791.3","gene_symbol":"AC007365.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64665607,"end":64666064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280332.1","gene_symbol":"AC020917.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16356329,"end":16358327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143502.14","gene_symbol":"SUSD4","gene_name":"sushi domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25470]","synonyms":"FLJ10052","biotype":"protein_coding","ncbi_id":"55061","summary":null,"start":223220819,"end":223364202,"strand":-1,"description":"sushi domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25470]"}, {"versioned_ensembl_gene_id":"ENSG00000179833.4","gene_symbol":"SERTAD2","gene_name":"SERTA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30784]","synonyms":"TRIP-Br2,Sei-2,KIAA0127","biotype":"protein_coding","ncbi_id":"9792","summary":null,"start":64631621,"end":64751005,"strand":-1,"description":"SERTA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30784]"}, {"versioned_ensembl_gene_id":"ENSG00000253985.1","gene_symbol":"AC145141.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71372676,"end":71374898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249981.1","gene_symbol":"AC145141.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71445616,"end":71446569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225048.1","gene_symbol":"CR759835.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026690,"end":29027617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127527.13","gene_symbol":"EPS15L1","gene_name":"epidermal growth factor receptor pathway substrate 15 like 1 [Source:HGNC Symbol;Acc:HGNC:24634]","synonyms":"eps15R","biotype":"protein_coding","ncbi_id":"58513","summary":null,"start":16355239,"end":16472085,"strand":-1,"description":"epidermal growth factor receptor pathway substrate 15 like 1 [Source:HGNC Symbol;Acc:HGNC:24634]"}, {"versioned_ensembl_gene_id":"ENSG00000250387.2","gene_symbol":"LINC02197","gene_name":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724392","summary":null,"start":71351855,"end":71446342,"strand":-1,"description":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]"}, {"versioned_ensembl_gene_id":"ENSG00000260172.1","gene_symbol":"LINC01413","gene_name":"long intergenic non-protein coding RNA 1413 [Source:HGNC Symbol;Acc:HGNC:50705]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928611","summary":null,"start":57319138,"end":57323908,"strand":1,"description":"long intergenic non-protein coding RNA 1413 [Source:HGNC Symbol;Acc:HGNC:50705]"}, {"versioned_ensembl_gene_id":"ENSG00000280670.2","gene_symbol":"CCDC163","gene_name":"coiled-coil domain containing 163 [Source:HGNC Symbol;Acc:HGNC:27003]","synonyms":"LOC126661,CCDC163P,C1orf231","biotype":"protein_coding","ncbi_id":"126661","summary":null,"start":45493866,"end":45500079,"strand":-1,"description":"coiled-coil domain containing 163 [Source:HGNC Symbol;Acc:HGNC:27003]"}, {"versioned_ensembl_gene_id":"ENSG00000224272.2","gene_symbol":"AC131097.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241808312,"end":241812016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226756.1","gene_symbol":"AC007365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64644612,"end":64646698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152086.8","gene_symbol":"TUBA3E","gene_name":"tubulin alpha 3e [Source:HGNC Symbol;Acc:HGNC:20765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"112714","summary":"Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulin. The genes encoding these microtubule constituents are part of the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. This gene encodes an alpha tubulin that highly conserved among species. A missense mutation in this gene has been potentially linked to microlissencephaly and global developmental delay. [provided by RefSeq, Jul 2016]","start":130191743,"end":130198461,"strand":-1,"description":"tubulin alpha 3e [Source:HGNC Symbol;Acc:HGNC:20765]"}, {"versioned_ensembl_gene_id":"ENSG00000161011.19","gene_symbol":"SQSTM1","gene_name":"sequestosome 1 [Source:HGNC Symbol;Acc:HGNC:11280]","synonyms":"PDB3,p62B,p62,p60,OSIL,A170","biotype":"protein_coding","ncbi_id":"8878","summary":"This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]","start":179806398,"end":179838078,"strand":1,"description":"sequestosome 1 [Source:HGNC Symbol;Acc:HGNC:11280]"}, {"versioned_ensembl_gene_id":"ENSG00000260870.1","gene_symbol":"NDUFB10P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52272]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128711","summary":null,"start":57325472,"end":57326447,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52272]"}, {"versioned_ensembl_gene_id":"ENSG00000262497.1","gene_symbol":"FAM187B2P","gene_name":"family with sequence similarity 187 member B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49213]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421621","summary":null,"start":35232291,"end":35233003,"strand":-1,"description":"family with sequence similarity 187 member B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49213]"}, {"versioned_ensembl_gene_id":"ENSG00000237089.2","gene_symbol":"PCNPP4","gene_name":"PEST containing nuclear protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874220","summary":null,"start":75537547,"end":75538702,"strand":-1,"description":"PEST containing nuclear protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41976]"}, {"versioned_ensembl_gene_id":"ENSG00000273113.1","gene_symbol":"AC133528.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241581922,"end":241582726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215023.2","gene_symbol":"AC131097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241800916,"end":241801907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224775.2","gene_symbol":"BRAFP1","gene_name":"BRAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18615]","synonyms":"BRAFPS2,BRAF2","biotype":"unprocessed_pseudogene","ncbi_id":"286494","summary":null,"start":75582676,"end":75585506,"strand":1,"description":"BRAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18615]"}, {"versioned_ensembl_gene_id":"ENSG00000204099.11","gene_symbol":"NEU4","gene_name":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]","synonyms":null,"biotype":"protein_coding","ncbi_id":"129807","summary":"The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2009]","start":241808825,"end":241817413,"strand":1,"description":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]"}, {"versioned_ensembl_gene_id":"ENSG00000170324.20","gene_symbol":"FRMPD2","gene_name":"FERM and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28572]","synonyms":"PDZK5C,PDZD5C,MGC35285","biotype":"protein_coding","ncbi_id":"143162","summary":"This gene encodes a peripheral membrane protein and is located in a region of chromosome 10q that contains a segmental duplication. This copy of the gene is full-length and is in the telomeric duplicated region. Two other more centromerically proximal copies of the gene are partial and may represent pseudogenes. This full-length gene appears to function in the establishment and maintenance of cell polarization. The protein is recruited to cell-cell junctions in an E-cadherin-dependent manner, and is selectively localized at the basolateral membrane in polarized epithelial cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2009]","start":48153088,"end":48274870,"strand":-1,"description":"FERM and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28572]"}, {"versioned_ensembl_gene_id":"ENSG00000235645.2","gene_symbol":"AL450311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69684899,"end":69692452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186082.9","gene_symbol":"KRT18P14","gene_name":"keratin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6433]","synonyms":"KRT18L4","biotype":"processed_pseudogene","ncbi_id":"119722","summary":null,"start":35860249,"end":35861498,"strand":-1,"description":"keratin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6433]"}, {"versioned_ensembl_gene_id":"ENSG00000254919.1","gene_symbol":"AC090692.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35915051,"end":35918739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250928.1","gene_symbol":"AC008629.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119011471,"end":119012056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261678.2","gene_symbol":"SCRT1","gene_name":"scratch family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:15950]","synonyms":"ZNF898,DKFZp547F072","biotype":"protein_coding","ncbi_id":"83482","summary":"This gene encodes a C2H2-type zinc finger transcriptional repressor that binds to E-box motifs. The encoded protein may promote neural differention and may be involved in cancers with neuroendocrine features. [provided by RefSeq, Jul 2013]","start":144330565,"end":144336281,"strand":-1,"description":"scratch family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:15950]"}, {"versioned_ensembl_gene_id":"ENSG00000135722.8","gene_symbol":"FBXL8","gene_name":"F-box and leucine rich repeat protein 8 [Source:HGNC Symbol;Acc:HGNC:17875]","synonyms":"Fbl8","biotype":"protein_coding","ncbi_id":"55336","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class. It shares 78% sequence identity with the mouse protein. [provided by RefSeq, Jul 2008]","start":67159931,"end":67164570,"strand":1,"description":"F-box and leucine rich repeat protein 8 [Source:HGNC Symbol;Acc:HGNC:17875]"}, {"versioned_ensembl_gene_id":"ENSG00000250678.1","gene_symbol":"AC008629.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119010060,"end":119010542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248979.2","gene_symbol":"LAMTOR3P2","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874516","summary":null,"start":119132651,"end":119132882,"strand":-1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39727]"}, {"versioned_ensembl_gene_id":"ENSG00000230469.1","gene_symbol":"RPL5P26","gene_name":"ribosomal protein L5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36247]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271206","summary":null,"start":69778962,"end":69779838,"strand":1,"description":"ribosomal protein L5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36247]"}, {"versioned_ensembl_gene_id":"ENSG00000226194.5","gene_symbol":"LINC02519","gene_name":"long intergenic non-protein coding RNA 2519 [Source:HGNC Symbol;Acc:HGNC:53510]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378147","summary":null,"start":169369998,"end":169388385,"strand":-1,"description":"long intergenic non-protein coding RNA 2519 [Source:HGNC Symbol;Acc:HGNC:53510]"}, {"versioned_ensembl_gene_id":"ENSG00000196275.13","gene_symbol":"GTF2IRD2","gene_name":"GTF2I repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30775]","synonyms":"GTF2IRD2A,FLJ37938","biotype":"protein_coding","ncbi_id":"84163","summary":"This gene is one of several closely related genes on chromosome 7 encoding proteins containing helix-loop-helix motifs. These proteins may function as regulators of transcription. The encoded protein is unique in that its C-terminus is derived from CHARLIE8 transposable element sequence. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, and loss of this locus may contribute to the cognitive phenotypes observed in this disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":74796144,"end":74851551,"strand":-1,"description":"GTF2I repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30775]"}, {"versioned_ensembl_gene_id":"ENSG00000230756.1","gene_symbol":"RHOQP3","gene_name":"ras homolog family member Q pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37837]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284988","summary":null,"start":130212870,"end":130213490,"strand":-1,"description":"ras homolog family member Q pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37837]"}, {"versioned_ensembl_gene_id":"ENSG00000274423.1","gene_symbol":"AC242843.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149345661,"end":149357612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213225.7","gene_symbol":"NOC2LP1","gene_name":"NOC2 like nucleolar associated transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52285]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"643276","summary":null,"start":130229379,"end":130232106,"strand":1,"description":"NOC2 like nucleolar associated transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52285]"}, {"versioned_ensembl_gene_id":"ENSG00000140396.12","gene_symbol":"NCOA2","gene_name":"nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:7669]","synonyms":"TIF2,NCoA-2,KAT13C,GRIP1,bHLHe75","biotype":"protein_coding","ncbi_id":"10499","summary":"The protein encoded by this gene functions as a transcriptional coactivator for nuclear hormone receptors, including steroid, thyroid, retinoid, and vitamin D receptors. The encoded protein acts as an intermediary factor for the ligand-dependent activity of these nuclear receptors, which regulate their target genes upon binding of cognate response elements. This gene has been found to be involved in translocations that result in fusions with other genes in various cancers, including the lysine acetyltransferase 6A (KAT6A) gene in acute myeloid leukemia, the ETS variant 6 (ETV6) gene in acute lymphoblastic leukemia, and the hes related family bHLH transcription factor with YRPW motif 1 (HEY1) gene in mesenchymal chondrosarcoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":70109762,"end":70403805,"strand":-1,"description":"nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:7669]"}, {"versioned_ensembl_gene_id":"ENSG00000225415.2","gene_symbol":"CCRL1P1","gene_name":"C-C motif chemokine receptor like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21142]","synonyms":"dJ509I19.4,CCRL1P","biotype":"processed_pseudogene","ncbi_id":"285737","summary":null,"start":138822747,"end":138823799,"strand":1,"description":"C-C motif chemokine receptor like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21142]"}, {"versioned_ensembl_gene_id":"ENSG00000253197.5","gene_symbol":"AC117834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92882984,"end":92965645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273819.1","gene_symbol":"ENPP7P7","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48690]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421859","summary":null,"start":67812557,"end":67873367,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48690]"}, {"versioned_ensembl_gene_id":"ENSG00000251347.2","gene_symbol":"IRF5P1","gene_name":"interferon regulatory factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41981]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420406","summary":null,"start":92972575,"end":92974738,"strand":1,"description":"interferon regulatory factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41981]"}, {"versioned_ensembl_gene_id":"ENSG00000254792.1","gene_symbol":"AP003716.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67840942,"end":67841049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276377.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22431917,"end":22432206,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199683.1","gene_symbol":"RN7SKP185","gene_name":"RNA, 7SK small nuclear pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:45909]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479178","summary":null,"start":37975156,"end":37975481,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:45909]"}, {"versioned_ensembl_gene_id":"ENSG00000239129.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29883006,"end":29883109,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000252594.1","gene_symbol":"RNU6-656P","gene_name":"RNA, U6 small nuclear 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:47619]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479857","summary":null,"start":46831050,"end":46831156,"strand":1,"description":"RNA, U6 small nuclear 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:47619]"}, {"versioned_ensembl_gene_id":"ENSG00000274359.1","gene_symbol":"AC012314.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221633.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":109018909,"end":109019116,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000276134.1","gene_symbol":"RN7SKP117","gene_name":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479147","summary":null,"start":125350868,"end":125351131,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]"}, {"versioned_ensembl_gene_id":"ENSG00000202537.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":86347062,"end":86347195,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000207433.1","gene_symbol":"RNU6-246P","gene_name":"RNA, U6 small nuclear 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:47209]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481884","summary":null,"start":15544188,"end":15544294,"strand":1,"description":"RNA, U6 small nuclear 246, pseudogene [Source:HGNC Symbol;Acc:HGNC:47209]"}, {"versioned_ensembl_gene_id":"ENSG00000199536.1","gene_symbol":"RNU6-315P","gene_name":"RNA, U6 small nuclear 315, pseudogene [Source:HGNC Symbol;Acc:HGNC:47278]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479707","summary":null,"start":170149845,"end":170149951,"strand":1,"description":"RNA, U6 small nuclear 315, pseudogene [Source:HGNC Symbol;Acc:HGNC:47278]"}, {"versioned_ensembl_gene_id":"ENSG00000202193.1","gene_symbol":"RNA5SP427","gene_name":"RNA, 5S ribosomal pseudogene 427 [Source:HGNC Symbol;Acc:HGNC:43327]","synonyms":"RN5S427","biotype":"rRNA","ncbi_id":"100873678","summary":null,"start":53337453,"end":53337571,"strand":1,"description":"RNA, 5S ribosomal pseudogene 427 [Source:HGNC Symbol;Acc:HGNC:43327]"}, {"versioned_ensembl_gene_id":"ENSG00000278773.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30061080,"end":30061183,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000202177.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101955077,"end":101955185,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207245.1","gene_symbol":"SNORD116-29","gene_name":"small nucleolar RNA, C/D box 116-29 [Source:HGNC Symbol;Acc:HGNC:33348]","synonyms":"HBII-85-29","biotype":"snoRNA","ncbi_id":"100033821","summary":null,"start":25106521,"end":25106603,"strand":1,"description":"small nucleolar RNA, C/D box 116-29 [Source:HGNC Symbol;Acc:HGNC:33348]"}, {"versioned_ensembl_gene_id":"ENSG00000280549.1","gene_symbol":"PADI3","gene_name":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]","synonyms":"PDI3","biotype":"protein_coding","ncbi_id":"51702","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type III enzyme modulates hair structural proteins, such as filaggrin in the hair follicle and trichohyalin in the inner root sheath, during hair follicle formation. Together with the type I enzyme, this enzyme may also play a role in terminal differentiation of the epidermis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17249098,"end":17284233,"strand":1,"description":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]"}, {"versioned_ensembl_gene_id":"ENSG00000252714.1","gene_symbol":"RNA5SP392","gene_name":"RNA, 5S ribosomal pseudogene 392 [Source:HGNC Symbol;Acc:HGNC:43292]","synonyms":"RN5S392","biotype":"rRNA","ncbi_id":"100873645","summary":null,"start":40331537,"end":40331648,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 392 [Source:HGNC Symbol;Acc:HGNC:43292]"}, {"versioned_ensembl_gene_id":"ENSG00000263597.1","gene_symbol":"MIR3936","gene_name":"microRNA 3936 [Source:HGNC Symbol;Acc:HGNC:38947]","synonyms":"hsa-mir-3936","biotype":"miRNA","ncbi_id":"100500865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132365490,"end":132365599,"strand":-1,"description":"microRNA 3936 [Source:HGNC Symbol;Acc:HGNC:38947]"}, {"versioned_ensembl_gene_id":"ENSG00000222094.1","gene_symbol":"RNU2-65P","gene_name":"RNA, U2 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48558]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480226","summary":null,"start":72045183,"end":72045367,"strand":1,"description":"RNA, U2 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48558]"}, {"versioned_ensembl_gene_id":"ENSG00000200626.1","gene_symbol":"RNA5SP325","gene_name":"RNA, 5S ribosomal pseudogene 325 [Source:HGNC Symbol;Acc:HGNC:43225]","synonyms":"RN5S325","biotype":"rRNA","ncbi_id":"100873591","summary":null,"start":106970021,"end":106970150,"strand":1,"description":"RNA, 5S ribosomal pseudogene 325 [Source:HGNC Symbol;Acc:HGNC:43225]"}, {"versioned_ensembl_gene_id":"ENSG00000202495.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50171197,"end":50171297,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212136.1","gene_symbol":"RNU6-696P","gene_name":"RNA, U6 small nuclear 696, pseudogene [Source:HGNC Symbol;Acc:HGNC:47659]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479873","summary":null,"start":37045530,"end":37045636,"strand":1,"description":"RNA, U6 small nuclear 696, pseudogene [Source:HGNC Symbol;Acc:HGNC:47659]"}, {"versioned_ensembl_gene_id":"ENSG00000222940.1","gene_symbol":"RNU6-370P","gene_name":"RNA, U6 small nuclear 370, pseudogene [Source:HGNC Symbol;Acc:HGNC:47333]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481295","summary":null,"start":24045835,"end":24045938,"strand":1,"description":"RNA, U6 small nuclear 370, pseudogene [Source:HGNC Symbol;Acc:HGNC:47333]"}, {"versioned_ensembl_gene_id":"ENSG00000264788.1","gene_symbol":"MIR3148","gene_name":"microRNA 3148 [Source:HGNC Symbol;Acc:HGNC:38215]","synonyms":"hsa-mir-3148","biotype":"miRNA","ncbi_id":"100422876","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29957272,"end":29957348,"strand":-1,"description":"microRNA 3148 [Source:HGNC Symbol;Acc:HGNC:38215]"}, {"versioned_ensembl_gene_id":"ENSG00000252637.1","gene_symbol":"RNA5SP268","gene_name":"RNA, 5S ribosomal pseudogene 268 [Source:HGNC Symbol;Acc:HGNC:43168]","synonyms":"RN5S268","biotype":"rRNA","ncbi_id":"100873521","summary":null,"start":67099302,"end":67099425,"strand":1,"description":"RNA, 5S ribosomal pseudogene 268 [Source:HGNC Symbol;Acc:HGNC:43168]"}, {"versioned_ensembl_gene_id":"ENSG00000283792.1","gene_symbol":"MIR4453","gene_name":"microRNA 4453 [Source:HGNC Symbol;Acc:HGNC:41892]","synonyms":"hsa-mir-4453","biotype":"miRNA","ncbi_id":"100616193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152536428,"end":152536516,"strand":1,"description":"microRNA 4453 [Source:HGNC Symbol;Acc:HGNC:41892]"}, {"versioned_ensembl_gene_id":"ENSG00000199673.1","gene_symbol":"SNORD16","gene_name":"small nucleolar RNA, C/D box 16 [Source:HGNC Symbol;Acc:HGNC:32712]","synonyms":"U16","biotype":"snoRNA","ncbi_id":"595097","summary":null,"start":66502812,"end":66502910,"strand":-1,"description":"small nucleolar RNA, C/D box 16 [Source:HGNC Symbol;Acc:HGNC:32712]"}, {"versioned_ensembl_gene_id":"ENSG00000207274.1","gene_symbol":"SNORA70I","gene_name":"small nucleolar RNA, H/ACA box 70I [Source:HGNC Symbol;Acc:HGNC:52215]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617008","summary":null,"start":214846947,"end":214847081,"strand":1,"description":"small nucleolar RNA, H/ACA box 70I [Source:HGNC Symbol;Acc:HGNC:52215]"}, {"versioned_ensembl_gene_id":"ENSG00000277999.1","gene_symbol":"AC009093.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29272220,"end":29272772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238242.1","gene_symbol":"AC097066.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60114875,"end":60149679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222854.1","gene_symbol":"RNA5SP59","gene_name":"RNA, 5S ribosomal pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:42836]","synonyms":"RN5S59","biotype":"rRNA","ncbi_id":"106480357","summary":null,"start":144701050,"end":144701159,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:42836]"}, {"versioned_ensembl_gene_id":"ENSG00000276031.1","gene_symbol":"RN7SL197P","gene_name":"RNA, 7SL, cytoplasmic 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:46213]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480975","summary":null,"start":49721949,"end":49722247,"strand":1,"description":"RNA, 7SL, cytoplasmic 197, pseudogene [Source:HGNC Symbol;Acc:HGNC:46213]"}, {"versioned_ensembl_gene_id":"ENSG00000274062.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43284139,"end":43284329,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000238387.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":9578028,"end":9578131,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000266515.1","gene_symbol":"MIR4452","gene_name":"microRNA 4452 [Source:HGNC Symbol;Acc:HGNC:41539]","synonyms":"hsa-mir-4452","biotype":"miRNA","ncbi_id":"100616463","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86542482,"end":86542552,"strand":-1,"description":"microRNA 4452 [Source:HGNC Symbol;Acc:HGNC:41539]"}, {"versioned_ensembl_gene_id":"ENSG00000273882.1","gene_symbol":"MIR8066","gene_name":"microRNA 8066 [Source:HGNC Symbol;Acc:HGNC:50043]","synonyms":"hsa-mir-8066","biotype":"miRNA","ncbi_id":"102465868","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101240795,"end":101240872,"strand":-1,"description":"microRNA 8066 [Source:HGNC Symbol;Acc:HGNC:50043]"}, {"versioned_ensembl_gene_id":"ENSG00000276700.1","gene_symbol":"RNA5-8S5","gene_name":"RNA, 5.8S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:37660]","synonyms":"RN5-8S1","biotype":"rRNA","ncbi_id":"110255170","summary":null,"start":128877,"end":129029,"strand":1,"description":"RNA, 5.8S ribosomal 5 [Source:HGNC Symbol;Acc:HGNC:37660]"}, {"versioned_ensembl_gene_id":"ENSG00000239249.3","gene_symbol":"RN7SL757P","gene_name":"RNA, 7SL, cytoplasmic 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:46773]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480530","summary":null,"start":28056153,"end":28056453,"strand":-1,"description":"RNA, 7SL, cytoplasmic 757, pseudogene [Source:HGNC Symbol;Acc:HGNC:46773]"}, {"versioned_ensembl_gene_id":"ENSG00000201363.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44344839,"end":44344933,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199732.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96309221,"end":96309322,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207281.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40339059,"end":40339164,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263367.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31127920,"end":31128019,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207552.1","gene_symbol":"MIR633","gene_name":"microRNA 633 [Source:HGNC Symbol;Acc:HGNC:32889]","synonyms":"MIRN633,hsa-mir-633","biotype":"miRNA","ncbi_id":"693218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62944215,"end":62944312,"strand":1,"description":"microRNA 633 [Source:HGNC Symbol;Acc:HGNC:32889]"}, {"versioned_ensembl_gene_id":"ENSG00000278055.1","gene_symbol":"MESTIT1_2","gene_name":"MEST intronic transcript 1, antisense RNA conserved region 2 [Source:RFAM;Acc:RF02149]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130488304,"end":130488538,"strand":1,"description":"MEST intronic transcript 1, antisense RNA conserved region 2 [Source:RFAM;Acc:RF02149]"}, {"versioned_ensembl_gene_id":"ENSG00000201176.1","gene_symbol":"RNU6-853P","gene_name":"RNA, U6 small nuclear 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:47816]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479943","summary":null,"start":168885355,"end":168885461,"strand":1,"description":"RNA, U6 small nuclear 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:47816]"}, {"versioned_ensembl_gene_id":"ENSG00000202092.1","gene_symbol":"RNA5SP190","gene_name":"RNA, 5S ribosomal pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:43090]","synonyms":"RN5S190","biotype":"rRNA","ncbi_id":"100873452","summary":null,"start":119445716,"end":119445833,"strand":1,"description":"RNA, 5S ribosomal pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:43090]"}, {"versioned_ensembl_gene_id":"ENSG00000281311.1","gene_symbol":"SNORA50","gene_name":"Small nucleolar RNA SNORA50 [Source:RFAM;Acc:RF00407]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64146337,"end":64146471,"strand":1,"description":"Small nucleolar RNA SNORA50 [Source:RFAM;Acc:RF00407]"}, {"versioned_ensembl_gene_id":"ENSG00000200227.1","gene_symbol":"RNA5SP197","gene_name":"RNA, 5S ribosomal pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:43097]","synonyms":"RN5S197","biotype":"rRNA","ncbi_id":"100873459","summary":null,"start":151477459,"end":151477577,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:43097]"}, {"versioned_ensembl_gene_id":"ENSG00000222659.1","gene_symbol":"RNU2-8P","gene_name":"RNA, U2 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48501]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480200","summary":null,"start":121580332,"end":121580521,"strand":-1,"description":"RNA, U2 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:48501]"}, {"versioned_ensembl_gene_id":"ENSG00000238908.1","gene_symbol":"RNA5SP484","gene_name":"RNA, 5S ribosomal pseudogene 484 [Source:HGNC Symbol;Acc:HGNC:43384]","synonyms":"RN5S484","biotype":"rRNA","ncbi_id":"100873726","summary":null,"start":40854119,"end":40854229,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 484 [Source:HGNC Symbol;Acc:HGNC:43384]"}, {"versioned_ensembl_gene_id":"ENSG00000276132.1","gene_symbol":"snoZ278","gene_name":"Small nucleolar RNA Z278 [Source:RFAM;Acc:RF00201]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29375114,"end":29375225,"strand":1,"description":"Small nucleolar RNA Z278 [Source:RFAM;Acc:RF00201]"}, {"versioned_ensembl_gene_id":"ENSG00000212269.1","gene_symbol":"RNU6-788P","gene_name":"RNA, U6 small nuclear 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:47751]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480609","summary":null,"start":23641489,"end":23641592,"strand":-1,"description":"RNA, U6 small nuclear 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:47751]"}, {"versioned_ensembl_gene_id":"ENSG00000276055.1","gene_symbol":"CLRN1-AS1","gene_name":"CLRN1 antisense RNA 1 conserved region [Source:RFAM;Acc:RF02089]","synonyms":"UCRP,CLRN1OS","biotype":"misc_RNA","ncbi_id":"116933","summary":null,"start":151079506,"end":151079584,"strand":1,"description":"CLRN1 antisense RNA 1 conserved region [Source:RFAM;Acc:RF02089]"}, {"versioned_ensembl_gene_id":"ENSG00000201737.1","gene_symbol":"RNU1-133P","gene_name":"RNA, U1 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48475]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481631","summary":null,"start":200775584,"end":200775750,"strand":1,"description":"RNA, U1 small nuclear 133, pseudogene [Source:HGNC Symbol;Acc:HGNC:48475]"}, {"versioned_ensembl_gene_id":"ENSG00000263600.1","gene_symbol":"MIR3915","gene_name":"microRNA 3915 [Source:HGNC Symbol;Acc:HGNC:38955]","synonyms":"hsa-mir-3915","biotype":"miRNA","ncbi_id":"100500915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32583656,"end":32583752,"strand":-1,"description":"microRNA 3915 [Source:HGNC Symbol;Acc:HGNC:38955]"}, {"versioned_ensembl_gene_id":"ENSG00000263861.1","gene_symbol":"MIR3927","gene_name":"microRNA 3927 [Source:HGNC Symbol;Acc:HGNC:38901]","synonyms":"hsa-mir-3927","biotype":"miRNA","ncbi_id":"100500898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109511475,"end":109511545,"strand":-1,"description":"microRNA 3927 [Source:HGNC Symbol;Acc:HGNC:38901]"}, {"versioned_ensembl_gene_id":"ENSG00000265942.2","gene_symbol":"RN7SL577P","gene_name":"RNA, 7SL, cytoplasmic 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:46593]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481080","summary":null,"start":49042341,"end":49042643,"strand":-1,"description":"RNA, 7SL, cytoplasmic 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:46593]"}, {"versioned_ensembl_gene_id":"ENSG00000265507.1","gene_symbol":"MIR4435-1","gene_name":"microRNA 4435-1 [Source:HGNC Symbol;Acc:HGNC:41713]","synonyms":"hsa-mir-4435-1","biotype":"miRNA","ncbi_id":"100616499","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87629755,"end":87629834,"strand":1,"description":"microRNA 4435-1 [Source:HGNC Symbol;Acc:HGNC:41713]"}, {"versioned_ensembl_gene_id":"ENSG00000199912.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7800361,"end":7800467,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211591.1","gene_symbol":"MIR762","gene_name":"microRNA 762 [Source:HGNC Symbol;Acc:HGNC:37303]","synonyms":"hsa-mir-762","biotype":"miRNA","ncbi_id":"100313837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30893903,"end":30893985,"strand":1,"description":"microRNA 762 [Source:HGNC Symbol;Acc:HGNC:37303]"}, {"versioned_ensembl_gene_id":"ENSG00000263581.1","gene_symbol":"MIR548X2","gene_name":"microRNA 548x-2 [Source:HGNC Symbol;Acc:HGNC:41734]","synonyms":"hsa-mir-548x-2","biotype":"miRNA","ncbi_id":"100616302","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65966330,"end":65966429,"strand":-1,"description":"microRNA 548x-2 [Source:HGNC Symbol;Acc:HGNC:41734]"}, {"versioned_ensembl_gene_id":"ENSG00000281434.2","gene_symbol":"NDUFA10","gene_name":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]","synonyms":"CI-42k","biotype":"protein_coding","ncbi_id":"4705","summary":"The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]","start":239892456,"end":240025408,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]"}, {"versioned_ensembl_gene_id":"ENSG00000200829.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20480844,"end":20480955,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222790.1","gene_symbol":"RNU4-14P","gene_name":"RNA, U4 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46950]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481176","summary":null,"start":140397323,"end":140397444,"strand":-1,"description":"RNA, U4 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46950]"}, {"versioned_ensembl_gene_id":"ENSG00000200975.1","gene_symbol":"RNU1-7P","gene_name":"RNA, U1 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:48306]","synonyms":"RNU1-7","biotype":"snRNA","ncbi_id":"106481952","summary":null,"start":8206434,"end":8206597,"strand":-1,"description":"RNA, U1 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:48306]"}, {"versioned_ensembl_gene_id":"ENSG00000212382.1","gene_symbol":"RNU6-159P","gene_name":"RNA, U6 small nuclear 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:47122]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480557","summary":null,"start":27863251,"end":27863356,"strand":1,"description":"RNA, U6 small nuclear 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:47122]"}, {"versioned_ensembl_gene_id":"ENSG00000251823.2","gene_symbol":"RNA5SP162","gene_name":"RNA, 5S ribosomal pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:43062]","synonyms":"RN5S162","biotype":"rRNA","ncbi_id":"100873427","summary":null,"start":228558296,"end":228558339,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:43062]"}, {"versioned_ensembl_gene_id":"ENSG00000284035.1","gene_symbol":"MIR5187","gene_name":"microRNA 5187 [Source:HGNC Symbol;Acc:HGNC:43523]","synonyms":"hsa-mir-5187","biotype":"miRNA","ncbi_id":"100847090","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":161227186,"end":161227261,"strand":1,"description":"microRNA 5187 [Source:HGNC Symbol;Acc:HGNC:43523]"}, {"versioned_ensembl_gene_id":"ENSG00000212446.1","gene_symbol":"RNU6-131P","gene_name":"RNA, U6 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:47094]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479624","summary":null,"start":44135883,"end":44135989,"strand":-1,"description":"RNA, U6 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:47094]"}, {"versioned_ensembl_gene_id":"ENSG00000274589.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18538885,"end":18539189,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253602.2","gene_symbol":"RN7SL260P","gene_name":"RNA, 7SL, cytoplasmic 260, pseudogene [Source:HGNC Symbol;Acc:HGNC:46276]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480497","summary":null,"start":142247585,"end":142247866,"strand":-1,"description":"RNA, 7SL, cytoplasmic 260, pseudogene [Source:HGNC Symbol;Acc:HGNC:46276]"}, {"versioned_ensembl_gene_id":"ENSG00000200764.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":207687960,"end":207688059,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221300.1","gene_symbol":"SNORD75","gene_name":"Small nucleolar RNA SNORD75 [Source:RFAM;Acc:RF00612]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692195","summary":null,"start":42440377,"end":42440436,"strand":1,"description":"Small nucleolar RNA SNORD75 [Source:RFAM;Acc:RF00612]"}, {"versioned_ensembl_gene_id":"ENSG00000283499.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":48109353,"end":48109410,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000274500.1","gene_symbol":"MESTIT1_3","gene_name":"MEST intronic transcript 1, antisense RNA conserved region 3 [Source:RFAM;Acc:RF02150]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130489868,"end":130489966,"strand":1,"description":"MEST intronic transcript 1, antisense RNA conserved region 3 [Source:RFAM;Acc:RF02150]"}, {"versioned_ensembl_gene_id":"ENSG00000200756.1","gene_symbol":"RNU6-236P","gene_name":"RNA, U6 small nuclear 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:47199]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481252","summary":null,"start":139717985,"end":139718090,"strand":-1,"description":"RNA, U6 small nuclear 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:47199]"}, {"versioned_ensembl_gene_id":"ENSG00000202335.1","gene_symbol":"SNORD50","gene_name":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":110496352,"end":110496421,"strand":-1,"description":"Small nucleolar RNA SNORD50 [Source:RFAM;Acc:RF00278]"}, {"versioned_ensembl_gene_id":"ENSG00000277660.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":90796,"end":90899,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000265558.1","gene_symbol":"MIR3918","gene_name":"microRNA 3918 [Source:HGNC Symbol;Acc:HGNC:38919]","synonyms":"hsa-mir-3918","biotype":"miRNA","ncbi_id":"100500851","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":158764661,"end":158764753,"strand":-1,"description":"microRNA 3918 [Source:HGNC Symbol;Acc:HGNC:38919]"}, {"versioned_ensembl_gene_id":"ENSG00000278049.1","gene_symbol":"ZNRD1-AS1_1","gene_name":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30031073,"end":30031140,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]"}, {"versioned_ensembl_gene_id":"ENSG00000251866.1","gene_symbol":"SCARNA21B","gene_name":"small Cajal body-specific RNA 21B [Source:HGNC Symbol;Acc:HGNC:52237]","synonyms":null,"biotype":"scaRNA","ncbi_id":"107397391","summary":null,"start":15542165,"end":15542304,"strand":1,"description":"small Cajal body-specific RNA 21B [Source:HGNC Symbol;Acc:HGNC:52237]"}, {"versioned_ensembl_gene_id":"ENSG00000266297.1","gene_symbol":"MIR744","gene_name":"microRNA 744 [Source:HGNC Symbol;Acc:HGNC:33658]","synonyms":"MIRN744,hsa-mir-744","biotype":"miRNA","ncbi_id":"100126313","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12081899,"end":12081996,"strand":1,"description":"microRNA 744 [Source:HGNC Symbol;Acc:HGNC:33658]"}, {"versioned_ensembl_gene_id":"ENSG00000207615.3","gene_symbol":"MIR515-2","gene_name":"microRNA 515-2 [Source:HGNC Symbol;Acc:HGNC:32097]","synonyms":"MIRN515-2,hsa-mir-515-2","biotype":"miRNA","ncbi_id":"574465","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53685009,"end":53685091,"strand":1,"description":"microRNA 515-2 [Source:HGNC Symbol;Acc:HGNC:32097]"}, {"versioned_ensembl_gene_id":"ENSG00000222419.1","gene_symbol":"RNA5SP511","gene_name":"RNA, 5S ribosomal pseudogene 511 [Source:HGNC Symbol;Acc:HGNC:43411]","synonyms":"RN5S511","biotype":"rRNA","ncbi_id":"100873562","summary":null,"start":103850797,"end":103850911,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 511 [Source:HGNC Symbol;Acc:HGNC:43411]"}, {"versioned_ensembl_gene_id":"ENSG00000244642.3","gene_symbol":"RN7SL396P","gene_name":"RNA, 7SL, cytoplasmic 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:46412]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479368","summary":null,"start":119862662,"end":119862956,"strand":1,"description":"RNA, 7SL, cytoplasmic 396, pseudogene [Source:HGNC Symbol;Acc:HGNC:46412]"}, {"versioned_ensembl_gene_id":"ENSG00000207383.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112579484,"end":112579584,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000231756.1","gene_symbol":"AL449983.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16473188,"end":16476237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283813.1","gene_symbol":"MIR4485","gene_name":"microRNA 4485 [Source:HGNC Symbol;Acc:HGNC:41628]","synonyms":"hsa-mir-4485","biotype":"miRNA","ncbi_id":"100616263","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10508270,"end":10508326,"strand":-1,"description":"microRNA 4485 [Source:HGNC Symbol;Acc:HGNC:41628]"}, {"versioned_ensembl_gene_id":"ENSG00000199701.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":94713715,"end":94713812,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222701.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30471587,"end":30471703,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251858.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":41594463,"end":41594591,"strand":1,"description":"Small nucleolar RNA 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Symbol;Acc:HGNC:23412]","synonyms":"LCN1L1,bA430N14.2","biotype":"unprocessed_pseudogene","ncbi_id":"286310","summary":null,"start":133224905,"end":133228591,"strand":-1,"description":"lipocalin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23412]"}, {"versioned_ensembl_gene_id":"ENSG00000241834.3","gene_symbol":"RN7SL149P","gene_name":"RNA, 7SL, cytoplasmic 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:46165]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480961","summary":null,"start":41840059,"end":41840339,"strand":-1,"description":"RNA, 7SL, cytoplasmic 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:46165]"}, {"versioned_ensembl_gene_id":"ENSG00000201984.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29139283,"end":29139384,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242985.3","gene_symbol":"RN7SL50P","gene_name":"RNA, 7SL, 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{"versioned_ensembl_gene_id":"ENSG00000284357.1","gene_symbol":"MIR34A","gene_name":"microRNA 34a [Source:HGNC Symbol;Acc:HGNC:31635]","synonyms":"MIRN34A,hsa-mir-34a","biotype":"miRNA","ncbi_id":"407040","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. This miRNA is a member of the highly conserved miR-34 family. This miRNA functions as a tumor suppressor and dysregulation or loss of the host gene from which this miRNA is processed is associated with cancer progression in numerous cell types. [provided by RefSeq, Sep 2015]","start":9151668,"end":9151777,"strand":-1,"description":"microRNA 34a [Source:HGNC Symbol;Acc:HGNC:31635]"}, {"versioned_ensembl_gene_id":"ENSG00000212529.1","gene_symbol":"SNORA57","gene_name":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]","synonyms":"U99","biotype":"snoRNA","ncbi_id":"692158","summary":null,"start":172252334,"end":172252478,"strand":-1,"description":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]"}, {"versioned_ensembl_gene_id":"ENSG00000253078.1","gene_symbol":"RNU6-1116P","gene_name":"RNA, U6 small nuclear 1116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48079]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480057","summary":null,"start":37435510,"end":37435608,"strand":-1,"description":"RNA, U6 small nuclear 1116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48079]"}, {"versioned_ensembl_gene_id":"ENSG00000222733.1","gene_symbol":"RNY4P29","gene_name":"RNA, Ro-associated Y4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42497]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873823","summary":null,"start":58527655,"end":58527751,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42497]"}, {"versioned_ensembl_gene_id":"ENSG00000201361.1","gene_symbol":"RNA5SP433","gene_name":"RNA, 5S ribosomal pseudogene 433 [Source:HGNC Symbol;Acc:HGNC:43333]","synonyms":"RN5S433","biotype":"rRNA","ncbi_id":"100873683","summary":null,"start":84262815,"end":84262928,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 433 [Source:HGNC Symbol;Acc:HGNC:43333]"}, {"versioned_ensembl_gene_id":"ENSG00000242201.3","gene_symbol":"RN7SL215P","gene_name":"RNA, 7SL, cytoplasmic 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:46231]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480980","summary":null,"start":194145674,"end":194145971,"strand":1,"description":"RNA, 7SL, cytoplasmic 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:46231]"}, {"versioned_ensembl_gene_id":"ENSG00000201393.1","gene_symbol":"SNORA71","gene_name":"Small nucleolar RNA SNORA71 [Source:RFAM;Acc:RF00056]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":78367507,"end":78367623,"strand":1,"description":"Small nucleolar RNA SNORA71 [Source:RFAM;Acc:RF00056]"}, {"versioned_ensembl_gene_id":"ENSG00000251704.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":16199203,"end":16199295,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000222998.1","gene_symbol":"RN7SKP259","gene_name":"RNA, 7SK small nuclear pseudogene 259 [Source:HGNC Symbol;Acc:HGNC:45983]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481751","summary":null,"start":57451690,"end":57452022,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 259 [Source:HGNC Symbol;Acc:HGNC:45983]"}, {"versioned_ensembl_gene_id":"ENSG00000265125.5","gene_symbol":"AC011824.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33565764,"end":33624122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183154.1","gene_symbol":"AC138356.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37734761,"end":37737426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207076.1","gene_symbol":"RNU6-1113P","gene_name":"RNA, U6 small nuclear 1113, pseudogene [Source:HGNC Symbol;Acc:HGNC:48076]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480056","summary":null,"start":43474186,"end":43474292,"strand":1,"description":"RNA, U6 small nuclear 1113, pseudogene [Source:HGNC Symbol;Acc:HGNC:48076]"}, {"versioned_ensembl_gene_id":"ENSG00000274703.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000251843.1","gene_symbol":"RNU6-803P","gene_name":"RNA, U6 small nuclear 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:47766]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481434","summary":null,"start":53719064,"end":53719165,"strand":-1,"description":"RNA, U6 small nuclear 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:47766]"}, {"versioned_ensembl_gene_id":"ENSG00000198972.3","gene_symbol":"MIRLET7E","gene_name":"microRNA let-7e [Source:HGNC Symbol;Acc:HGNC:31482]","synonyms":"MIRNLET7E,hsa-let-7e","biotype":"miRNA","ncbi_id":"406887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51692786,"end":51692864,"strand":1,"description":"microRNA let-7e [Source:HGNC Symbol;Acc:HGNC:31482]"}, {"versioned_ensembl_gene_id":"ENSG00000284094.1","gene_symbol":"MIR6073","gene_name":"microRNA 6073 [Source:HGNC Symbol;Acc:HGNC:50128]","synonyms":"hsa-mir-6073","biotype":"miRNA","ncbi_id":"102464826","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15969533,"end":15969621,"strand":-1,"description":"microRNA 6073 [Source:HGNC Symbol;Acc:HGNC:50128]"}, {"versioned_ensembl_gene_id":"ENSG00000202431.1","gene_symbol":"RNU6-438P","gene_name":"RNA, U6 small nuclear 438, pseudogene [Source:HGNC Symbol;Acc:HGNC:47401]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479760","summary":null,"start":34297496,"end":34297598,"strand":-1,"description":"RNA, U6 small nuclear 438, pseudogene [Source:HGNC Symbol;Acc:HGNC:47401]"}, {"versioned_ensembl_gene_id":"ENSG00000222511.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8796571,"end":8796673,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207271.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36626015,"end":36626138,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266760.1","gene_symbol":"MIR4464","gene_name":"microRNA 4464 [Source:HGNC Symbol;Acc:HGNC:41528]","synonyms":"hsa-mir-4464","biotype":"miRNA","ncbi_id":"100616109","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90312742,"end":90312833,"strand":1,"description":"microRNA 4464 [Source:HGNC Symbol;Acc:HGNC:41528]"}, {"versioned_ensembl_gene_id":"ENSG00000221332.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":75398860,"end":75399067,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000202191.1","gene_symbol":"SNORD113-1","gene_name":"small nucleolar RNA, C/D box 113-1 [Source:HGNC Symbol;Acc:HGNC:32980]","synonyms":"14q(I-1)","biotype":"snoRNA","ncbi_id":"767561","summary":"Small nucleolar RNAs (snoRNAs), like SNORD113-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD113-1 is 1 of 9 tandem SNORD113 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":100924824,"end":100924892,"strand":1,"description":"small nucleolar RNA, C/D box 113-1 [Source:HGNC Symbol;Acc:HGNC:32980]"}, {"versioned_ensembl_gene_id":"ENSG00000240203.3","gene_symbol":"RN7SL567P","gene_name":"RNA, 7SL, cytoplasmic 567, pseudogene [Source:HGNC Symbol;Acc:HGNC:46583]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481976","summary":null,"start":42676189,"end":42676491,"strand":-1,"description":"RNA, 7SL, cytoplasmic 567, pseudogene [Source:HGNC Symbol;Acc:HGNC:46583]"}, {"versioned_ensembl_gene_id":"ENSG00000266291.1","gene_symbol":"MIR3180-3","gene_name":"microRNA 3180-3 [Source:HGNC Symbol;Acc:HGNC:38239]","synonyms":"hsa-mir-3180-3","biotype":"miRNA","ncbi_id":"100422836","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18402178,"end":18402271,"strand":-1,"description":"microRNA 3180-3 [Source:HGNC Symbol;Acc:HGNC:38239]"}, {"versioned_ensembl_gene_id":"ENSG00000225758.1","gene_symbol":"RPS17P17","gene_name":"ribosomal protein S17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271230","summary":null,"start":140470866,"end":140471274,"strand":-1,"description":"ribosomal protein S17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35647]"}, {"versioned_ensembl_gene_id":"ENSG00000272717.1","gene_symbol":"AC112236.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139556799,"end":139557643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235968.1","gene_symbol":"AC079112.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68023694,"end":68024766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216099.3","gene_symbol":"MIR889","gene_name":"microRNA 889 [Source:HGNC Symbol;Acc:HGNC:33651]","synonyms":"MIRN889,hsa-mir-889","biotype":"miRNA","ncbi_id":"100126345","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101047901,"end":101047979,"strand":1,"description":"microRNA 889 [Source:HGNC Symbol;Acc:HGNC:33651]"}, {"versioned_ensembl_gene_id":"ENSG00000222365.1","gene_symbol":"SNORD12B","gene_name":"small nucleolar RNA, C/D box 12B [Source:HGNC Symbol;Acc:HGNC:33573]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113393","summary":null,"start":49280319,"end":49280409,"strand":1,"description":"small nucleolar RNA, C/D box 12B [Source:HGNC Symbol;Acc:HGNC:33573]"}, {"versioned_ensembl_gene_id":"ENSG00000275669.1","gene_symbol":"MIR6744","gene_name":"microRNA 6744 [Source:HGNC Symbol;Acc:HGNC:50051]","synonyms":"hsa-mir-6744","biotype":"miRNA","ncbi_id":"102466725","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1256605,"end":1256670,"strand":1,"description":"microRNA 6744 [Source:HGNC Symbol;Acc:HGNC:50051]"}, {"versioned_ensembl_gene_id":"ENSG00000201527.1","gene_symbol":"RNA5SP478","gene_name":"RNA, 5S ribosomal pseudogene 478 [Source:HGNC Symbol;Acc:HGNC:43378]","synonyms":"RN5S478","biotype":"rRNA","ncbi_id":"100873720","summary":null,"start":23160857,"end":23160971,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 478 [Source:HGNC Symbol;Acc:HGNC:43378]"}, {"versioned_ensembl_gene_id":"ENSG00000195401.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68735720,"end":68735823,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212172.1","gene_symbol":"RNU1-149P","gene_name":"RNA, U1 small nuclear 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48491]","synonyms":null,"biotype":"snRNA","ncbi_id":"107048983","summary":null,"start":22195469,"end":22195629,"strand":-1,"description":"RNA, U1 small nuclear 149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48491]"}, {"versioned_ensembl_gene_id":"ENSG00000201016.1","gene_symbol":"RNU6-374P","gene_name":"RNA, U6 small nuclear 374, pseudogene [Source:HGNC Symbol;Acc:HGNC:47337]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481296","summary":null,"start":25701217,"end":25701324,"strand":-1,"description":"RNA, U6 small nuclear 374, pseudogene [Source:HGNC Symbol;Acc:HGNC:47337]"}, {"versioned_ensembl_gene_id":"ENSG00000200941.1","gene_symbol":"RNU6-694P","gene_name":"RNA, U6 small nuclear 694, pseudogene [Source:HGNC Symbol;Acc:HGNC:47657]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479872","summary":null,"start":4386410,"end":4386556,"strand":-1,"description":"RNA, U6 small nuclear 694, pseudogene [Source:HGNC Symbol;Acc:HGNC:47657]"}, {"versioned_ensembl_gene_id":"ENSG00000202060.1","gene_symbol":"RNA5SP455","gene_name":"RNA, 5S ribosomal pseudogene 455 [Source:HGNC Symbol;Acc:HGNC:43355]","synonyms":"RN5S455","biotype":"rRNA","ncbi_id":"100873700","summary":null,"start":44071583,"end":44071701,"strand":1,"description":"RNA, 5S ribosomal pseudogene 455 [Source:HGNC Symbol;Acc:HGNC:43355]"}, {"versioned_ensembl_gene_id":"ENSG00000239555.3","gene_symbol":"RN7SL841P","gene_name":"RNA, 7SL, cytoplasmic 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:46857]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481150","summary":null,"start":55291379,"end":55291675,"strand":-1,"description":"RNA, 7SL, cytoplasmic 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:46857]"}, {"versioned_ensembl_gene_id":"ENSG00000207431.2","gene_symbol":"RNU6-906P","gene_name":"RNA, U6 small nuclear 906, pseudogene [Source:HGNC Symbol;Acc:HGNC:47869]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481465","summary":null,"start":146639700,"end":146639769,"strand":1,"description":"RNA, U6 small nuclear 906, pseudogene [Source:HGNC Symbol;Acc:HGNC:47869]"}, {"versioned_ensembl_gene_id":"ENSG00000201701.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":32037526,"end":32037653,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000239398.3","gene_symbol":"RN7SL342P","gene_name":"RNA, 7SL, cytoplasmic 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:46358]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479349","summary":null,"start":59972914,"end":59973207,"strand":1,"description":"RNA, 7SL, cytoplasmic 342, pseudogene [Source:HGNC Symbol;Acc:HGNC:46358]"}, {"versioned_ensembl_gene_id":"ENSG00000200871.1","gene_symbol":"RNU6-810P","gene_name":"RNA, U6 small nuclear 810, pseudogene [Source:HGNC Symbol;Acc:HGNC:47773]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481437","summary":null,"start":29134014,"end":29134120,"strand":1,"description":"RNA, U6 small nuclear 810, pseudogene [Source:HGNC Symbol;Acc:HGNC:47773]"}, {"versioned_ensembl_gene_id":"ENSG00000266410.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33177507,"end":33177602,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275859.1","gene_symbol":"MIR6720","gene_name":"microRNA 6720 [Source:HGNC Symbol;Acc:HGNC:50032]","synonyms":"hsa-mir-6720","biotype":"miRNA","ncbi_id":"102466720","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1390314,"end":1390411,"strand":-1,"description":"microRNA 6720 [Source:HGNC Symbol;Acc:HGNC:50032]"}, {"versioned_ensembl_gene_id":"ENSG00000202350.1","gene_symbol":"RNU6-326P","gene_name":"RNA, U6 small nuclear 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:47289]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481282","summary":null,"start":45843634,"end":45843740,"strand":1,"description":"RNA, U6 small nuclear 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:47289]"}, {"versioned_ensembl_gene_id":"ENSG00000202225.1","gene_symbol":"RNA5SP240","gene_name":"RNA, 5S ribosomal pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:43140]","synonyms":"RN5S240","biotype":"rRNA","ncbi_id":"100873498","summary":null,"start":120981426,"end":120981553,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 240 [Source:HGNC Symbol;Acc:HGNC:43140]"}, {"versioned_ensembl_gene_id":"ENSG00000120265.16","gene_symbol":"PCMT1","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8728]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5110","summary":"This gene encodes a member of the type II class of protein carboxyl methyltransferase enzymes. The encoded enzyme plays a role in protein repair by recognizing and converting D-aspartyl and L-isoaspartyl residues resulting from spontaneous deamidation back to the normal L-aspartyl form. The encoded protein may play a protective role in the pathogenesis of Alzheimer's disease, and single nucleotide polymorphisms in this gene have been associated with spina bifida and premature ovarian failure. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":149749443,"end":149811420,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8728]"}, {"versioned_ensembl_gene_id":"ENSG00000234718.7","gene_symbol":"AC007161.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":7738524,"end":7742574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284332.1","gene_symbol":"MIR1302-2","gene_name":"microRNA 1302-2 [Source:HGNC Symbol;Acc:HGNC:35294]","synonyms":"MIRN1302-2,hsa-mir-1302-2","biotype":"miRNA","ncbi_id":"100302278","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30366,"end":30503,"strand":1,"description":"microRNA 1302-2 [Source:HGNC Symbol;Acc:HGNC:35294]"}, {"versioned_ensembl_gene_id":"ENSG00000212204.1","gene_symbol":"RNA5SP91","gene_name":"RNA, 5S ribosomal pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:42889]","synonyms":"RN5S91","biotype":"rRNA","ncbi_id":"100873324","summary":null,"start":33285769,"end":33285887,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:42889]"}, {"versioned_ensembl_gene_id":"ENSG00000202428.1","gene_symbol":"RNU6-108P","gene_name":"RNA, U6 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:47071]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481875","summary":null,"start":57536252,"end":57536358,"strand":-1,"description":"RNA, U6 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:47071]"}, {"versioned_ensembl_gene_id":"ENSG00000158615.8","gene_symbol":"PPP1R15B","gene_name":"protein phosphatase 1 regulatory subunit 15B [Source:HGNC Symbol;Acc:HGNC:14951]","synonyms":"FLJ14744","biotype":"protein_coding","ncbi_id":"84919","summary":"This gene encodes a protein phosphatase I-interacting protein that promotes the dephosphorylation of eukaryotic translation initiation factor 2A to regulate translation under conditions of cellular stress. The transcribed messenger RNA contains two upstream open reading frames (ORFs) that repress translation of the main protein coding ORF under normal conditions, while the protein coding ORF is expressed at high levels in response to stress. Continual translation of the mRNA under conditions of eukaryotic translation initiation factor 2A inactivation is thought to create a feedback loop for reactivation of the gene during recovery from stress. In addition, it has been shown that this protein plays a role in membrane traffic that is independent of translation and that it is required for exocytosis from erythroleukemia cells. Allelic variants of this gene are associated with microcephaly, short stature, and impaired glucose metabolism. [provided by RefSeq, Feb 2016]","start":204403387,"end":204411791,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 15B [Source:HGNC Symbol;Acc:HGNC:14951]"}, {"versioned_ensembl_gene_id":"ENSG00000213409.4","gene_symbol":"C1QBPP2","gene_name":"complement C1q binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422299","summary":null,"start":66761575,"end":66762399,"strand":-1,"description":"complement C1q binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51618]"}, {"versioned_ensembl_gene_id":"ENSG00000268677.1","gene_symbol":"AC011495.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49688853,"end":49690573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258504.2","gene_symbol":"AL157871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100291117,"end":100294656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258982.1","gene_symbol":"AL133523.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100207407,"end":100238555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107282.7","gene_symbol":"APBA1","gene_name":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]","synonyms":"D9S411E,X11,MINT1","biotype":"protein_coding","ncbi_id":"320","summary":"The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a putative vesicular trafficking protein in the brain that can form a complex with the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. [provided by RefSeq, Jul 2008]","start":69427530,"end":69672306,"strand":-1,"description":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]"}, {"versioned_ensembl_gene_id":"ENSG00000240518.2","gene_symbol":"AC116353.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140609085,"end":140609400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108039.17","gene_symbol":"XPNPEP1","gene_name":"X-prolyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:12822]","synonyms":"XPNPEP,XPNPEPL1,XPNPEPL","biotype":"protein_coding","ncbi_id":"7511","summary":"This gene encodes the cytosolic form of a metalloaminopeptidase that catalyzes the cleavage of the N-terminal amino acid adjacent to a proline residue. The gene product may play a role in degradation and maturation of tachykinins, neuropeptides, and peptide hormones. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009]","start":109864766,"end":109923553,"strand":-1,"description":"X-prolyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:12822]"}, {"versioned_ensembl_gene_id":"ENSG00000013306.15","gene_symbol":"SLC25A39","gene_name":"solute carrier family 25 member 39 [Source:HGNC Symbol;Acc:HGNC:24279]","synonyms":"FLJ22407,CGI-69","biotype":"protein_coding","ncbi_id":"51629","summary":"This gene encodes a member of the SLC25 transporter or mitochondrial carrier family of proteins. Members of this family are encoded by the nuclear genome while their protein products are usually embedded in the inner mitochondrial membrane and exhibit wide-ranging substrate specificity. Although the encoded protein is currently considered an orphan transporter, this protein is related to other carriers known to transport amino acids. This protein may play a role in iron homeostasis. [provided by RefSeq, Mar 2016]","start":44319625,"end":44324870,"strand":-1,"description":"solute carrier family 25 member 39 [Source:HGNC Symbol;Acc:HGNC:24279]"}, {"versioned_ensembl_gene_id":"ENSG00000283155.1","gene_symbol":"AC116353.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":140562443,"end":140592123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283602.1","gene_symbol":"AC116353.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":140569962,"end":140594570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251453.1","gene_symbol":"HAUS1P1","gene_name":"HAUS augmin like complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43760]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728921","summary":null,"start":140581504,"end":140582335,"strand":1,"description":"HAUS augmin like complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43760]"}, {"versioned_ensembl_gene_id":"ENSG00000197694.15","gene_symbol":"SPTAN1","gene_name":"spectrin alpha, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11273]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6709","summary":"Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles. Spectrins are composed of alpha and beta dimers that associate to form tetramers linked in a head-to-head arrangement. This gene encodes an alpha spectrin that is specifically expressed in nonerythrocytic cells. The encoded protein has been implicated in other cellular functions including DNA repair and cell cycle regulation. Mutations in this gene are the cause of early infantile epileptic encephalopathy-5. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]","start":128552558,"end":128633662,"strand":1,"description":"spectrin alpha, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11273]"}, {"versioned_ensembl_gene_id":"ENSG00000233436.7","gene_symbol":"BTBD18","gene_name":"BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:37214]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643376","summary":null,"start":57743514,"end":57751781,"strand":-1,"description":"BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:37214]"}, {"versioned_ensembl_gene_id":"ENSG00000143318.12","gene_symbol":"CASQ1","gene_name":"calsequestrin 1 [Source:HGNC Symbol;Acc:HGNC:1512]","synonyms":"PDIB1,CASQ","biotype":"protein_coding","ncbi_id":"844","summary":"This gene encodes the skeletal muscle specific member of the calsequestrin protein family. Calsequestrin functions as a luminal sarcoplasmic reticulum calcium sensor in both cardiac and skeletal muscle cells. This protein, also known as calmitine, functions as a calcium regulator in the mitochondria of skeletal muscle. This protein is absent in patients with Duchenne and Becker types of muscular dystrophy. [provided by RefSeq, Jun 2013]","start":160190556,"end":160201886,"strand":1,"description":"calsequestrin 1 [Source:HGNC Symbol;Acc:HGNC:1512]"}, {"versioned_ensembl_gene_id":"ENSG00000183979.7","gene_symbol":"NPB","gene_name":"neuropeptide B [Source:HGNC Symbol;Acc:HGNC:30099]","synonyms":"PPNPB,PPL7","biotype":"protein_coding","ncbi_id":"256933","summary":"This gene encodes a member of the neuropeptide B/W family of proteins and preproprotein that is proteolytically processed to generate multiple protein products. The encoded products include neuropeptide B-23 and a C-terminally extended form, neuropeptide B-29, which are characterized by an N-terminal brominated tryptophan amino acid. Both of the encoded peptides bind with higher affinity to neuropeptide B/W (NPB/W) receptor 1 compared to the related NPB/W receptor 2. These peptides may regulate feeding, pain perception, and stress in rodents. [provided by RefSeq, Jul 2015]","start":81900745,"end":81902905,"strand":1,"description":"neuropeptide B [Source:HGNC Symbol;Acc:HGNC:30099]"}, {"versioned_ensembl_gene_id":"ENSG00000164331.9","gene_symbol":"ANKRA2","gene_name":"ankyrin repeat family A member 2 [Source:HGNC Symbol;Acc:HGNC:13208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57763","summary":null,"start":73552335,"end":73565686,"strand":-1,"description":"ankyrin repeat family A member 2 [Source:HGNC Symbol;Acc:HGNC:13208]"}, {"versioned_ensembl_gene_id":"ENSG00000227417.3","gene_symbol":"AC114402.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203805621,"end":203806263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243250.1","gene_symbol":"AP002884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112235371,"end":112236025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234648.1","gene_symbol":"AL162151.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98973314,"end":98973471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259119.1","gene_symbol":"AL132796.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98925137,"end":98927805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188783.5","gene_symbol":"PRELP","gene_name":"proline and arginine rich end leucine rich repeat protein [Source:HGNC Symbol;Acc:HGNC:9357]","synonyms":"SLRR2A,prolargin","biotype":"protein_coding","ncbi_id":"5549","summary":"The protein encoded by this gene is a leucine-rich repeat protein present in connective tissue extracellular matrix. This protein functions as a molecule anchoring basement membranes to the underlying connective tissue. This protein has been shown to bind type I collagen to basement membranes and type II collagen to cartilage. It also binds the basement membrane heparan sulfate proteoglycan perlecan. This protein is suggested to be involved in the pathogenesis of Hutchinson-Gilford progeria (HGP), which is reported to lack the binding of collagen in basement membranes and cartilage. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":203475828,"end":203491352,"strand":1,"description":"proline and arginine rich end leucine rich repeat protein [Source:HGNC Symbol;Acc:HGNC:9357]"}, {"versioned_ensembl_gene_id":"ENSG00000224160.1","gene_symbol":"CICP10","gene_name":"capicua transcriptional repressor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462787","summary":null,"start":242119856,"end":242120053,"strand":-1,"description":"capicua transcriptional repressor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37901]"}, {"versioned_ensembl_gene_id":"ENSG00000255807.1","gene_symbol":"PTP4A1P2","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499563","summary":null,"start":133033503,"end":133033956,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41929]"}, {"versioned_ensembl_gene_id":"ENSG00000259535.1","gene_symbol":"RPL21P12","gene_name":"ribosomal protein L21 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:19810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122409","summary":null,"start":103148597,"end":103149408,"strand":1,"description":"ribosomal protein L21 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:19810]"}, {"versioned_ensembl_gene_id":"ENSG00000139915.19","gene_symbol":"MDGA2","gene_name":"MAM domain containing glycosylphosphatidylinositol anchor 2 [Source:HGNC Symbol;Acc:HGNC:19835]","synonyms":"MAMDC1","biotype":"protein_coding","ncbi_id":"161357","summary":null,"start":46840092,"end":47674954,"strand":-1,"description":"MAM domain containing glycosylphosphatidylinositol anchor 2 [Source:HGNC Symbol;Acc:HGNC:19835]"}, {"versioned_ensembl_gene_id":"ENSG00000280119.1","gene_symbol":"AC093642.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":242001209,"end":242006013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237940.3","gene_symbol":"LINC01238","gene_name":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]","synonyms":"FLJ40615,FLJ40615","biotype":"lincRNA","ncbi_id":"102723927","summary":null,"start":241970683,"end":241977276,"strand":1,"description":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]"}, {"versioned_ensembl_gene_id":"ENSG00000226423.1","gene_symbol":"AC093642.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242025183,"end":242026176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240083.2","gene_symbol":"RPS3AP22","gene_name":"ribosomal protein S3a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36573]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130786","summary":null,"start":88381957,"end":88382725,"strand":1,"description":"ribosomal protein S3a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36573]"}, {"versioned_ensembl_gene_id":"ENSG00000250156.3","gene_symbol":"LINC02060","gene_name":"long intergenic non-protein coding RNA 2060 [Source:HGNC Symbol;Acc:HGNC:52904]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546226","summary":null,"start":88408982,"end":88439090,"strand":-1,"description":"long intergenic non-protein coding RNA 2060 [Source:HGNC Symbol;Acc:HGNC:52904]"}, {"versioned_ensembl_gene_id":"ENSG00000279259.1","gene_symbol":"AC087741.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80147250,"end":80148596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230684.1","gene_symbol":"AL158207.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129933536,"end":129936541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185215.8","gene_symbol":"TNFAIP2","gene_name":"TNF alpha induced protein 2 [Source:HGNC Symbol;Acc:HGNC:11895]","synonyms":"EXOC3L3,B94","biotype":"protein_coding","ncbi_id":"7127","summary":"This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. The expression of this gene was shown to be induced by retinoic acid in a cell line expressing a oncogenic version of the retinoic acid receptor alpha fusion protein, which suggested that this gene may be a retinoic acid target gene in acute promyelocytic leukemia. [provided by RefSeq, Jul 2008]","start":103123442,"end":103137439,"strand":1,"description":"TNF alpha induced protein 2 [Source:HGNC Symbol;Acc:HGNC:11895]"}, {"versioned_ensembl_gene_id":"ENSG00000186625.13","gene_symbol":"KATNA1","gene_name":"katanin catalytic subunit A1 [Source:HGNC Symbol;Acc:HGNC:6216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11104","summary":"Microtubules, polymers of alpha and beta tubulin subunits, form the mitotic spindle of a dividing cell and help to organize membranous organelles during interphase. Katanin is a heterodimer that consists of a 60 kDa ATPase (p60 subunit A 1) and an 80 kDa accessory protein (p80 subunit B 1). The p60 subunit acts to sever and disassemble microtubules, while the p80 subunit targets the enzyme to the centrosome. This gene encodes the p80 subunit. This protein is a member of the AAA family of ATPases. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2011]","start":149594873,"end":149648972,"strand":-1,"description":"katanin catalytic subunit A1 [Source:HGNC Symbol;Acc:HGNC:6216]"}, {"versioned_ensembl_gene_id":"ENSG00000258553.5","gene_symbol":"AL157911.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59969116,"end":60091783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258746.2","gene_symbol":"AL162632.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45502742,"end":45503140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225147.1","gene_symbol":"RPS12P10","gene_name":"ribosomal protein S12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35824]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271056","summary":null,"start":142566700,"end":142567076,"strand":1,"description":"ribosomal protein S12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35824]"}, {"versioned_ensembl_gene_id":"ENSG00000164151.11","gene_symbol":"ICE1","gene_name":"interactor of little elongation complex ELL subunit 1 [Source:HGNC Symbol;Acc:HGNC:29154]","synonyms":"KIAA0947","biotype":"protein_coding","ncbi_id":"23379","summary":null,"start":5420664,"end":5490234,"strand":1,"description":"interactor of little elongation complex ELL subunit 1 [Source:HGNC Symbol;Acc:HGNC:29154]"}, {"versioned_ensembl_gene_id":"ENSG00000173894.10","gene_symbol":"CBX2","gene_name":"chromobox 2 [Source:HGNC Symbol;Acc:HGNC:1552]","synonyms":"MGC10561,CDCA6","biotype":"protein_coding","ncbi_id":"84733","summary":"This gene encodes a component of the polycomb multiprotein complex, which is required to maintain the transcriptionally repressive state of many genes throughout development via chromatin remodeling and modification of histones. Disruption of this gene in mice results in male-to-female gonadal sex reversal. Mutations in this gene are also associated with gonadal dysgenesis in humans. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Mar 2010]","start":79778132,"end":79787983,"strand":1,"description":"chromobox 2 [Source:HGNC Symbol;Acc:HGNC:1552]"}, {"versioned_ensembl_gene_id":"ENSG00000241187.1","gene_symbol":"AC008379.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154729231,"end":154729694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055211.12","gene_symbol":"GINM1","gene_name":"glycoprotein integral membrane 1 [Source:HGNC Symbol;Acc:HGNC:21074]","synonyms":"dJ12G14.2,C6orf72","biotype":"protein_coding","ncbi_id":"116254","summary":null,"start":149566294,"end":149591748,"strand":1,"description":"glycoprotein integral membrane 1 [Source:HGNC Symbol;Acc:HGNC:21074]"}, {"versioned_ensembl_gene_id":"ENSG00000267890.1","gene_symbol":"AC010624.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50075123,"end":50075902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136816.15","gene_symbol":"TOR1B","gene_name":"torsin family 1 member B [Source:HGNC Symbol;Acc:HGNC:11995]","synonyms":"MGC4386,DQ1","biotype":"protein_coding","ncbi_id":"27348","summary":"The protein encoded by this gene is an ATPase found primarily in the endoplasmic reticulum and nuclear envelope. This gene has a highly-similar neighboring gene, TOR1A, that encodes a protein that is likely to interact in a complex with this protein. Finally, this protein may act as a chaperone and play a role in maintaining the integrity of the nuclear envelope and endoplasmic reticulum. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":129803153,"end":129811281,"strand":1,"description":"torsin family 1 member B [Source:HGNC Symbol;Acc:HGNC:11995]"}, {"versioned_ensembl_gene_id":"ENSG00000246640.1","gene_symbol":"PICART1","gene_name":"p53-inducible cancer-associated RNA transcript 1 [Source:NCBI gene;Acc:284080]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284080","summary":null,"start":50050349,"end":50055739,"strand":-1,"description":"p53-inducible cancer-associated RNA transcript 1 [Source:NCBI gene;Acc:284080]"}, {"versioned_ensembl_gene_id":"ENSG00000233909.1","gene_symbol":"UBE2V1P4","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44886]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724816","summary":null,"start":129791196,"end":129791837,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44886]"}, {"versioned_ensembl_gene_id":"ENSG00000228915.3","gene_symbol":"OR7E128P","gene_name":"olfactory receptor family 7 subfamily E member 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:15305]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81175","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71893410,"end":71894433,"strand":1,"description":"olfactory receptor family 7 subfamily E member 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:15305]"}, {"versioned_ensembl_gene_id":"ENSG00000275017.1","gene_symbol":"AL353748.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88391362,"end":88391832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250635.1","gene_symbol":"CXXC5-AS1","gene_name":"CXXC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53009]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139648999,"end":139649728,"strand":-1,"description":"CXXC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53009]"}, {"versioned_ensembl_gene_id":"ENSG00000069399.14","gene_symbol":"BCL3","gene_name":"B-cell CLL/lymphoma 3 [Source:HGNC Symbol;Acc:HGNC:998]","synonyms":"D19S37,BCL4","biotype":"protein_coding","ncbi_id":"602","summary":"This gene is a proto-oncogene candidate. It is identified by its translocation into the immunoglobulin alpha-locus in some cases of B-cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co-activator that activates through its association with NF-kappa B homodimers. The expression of this gene can be induced by NF-kappa B, which forms a part of the autoregulatory loop that controls the nuclear residence of p50 NF-kappa B. [provided by RefSeq, Jul 2008]","start":44747705,"end":44760044,"strand":1,"description":"B-cell CLL/lymphoma 3 [Source:HGNC Symbol;Acc:HGNC:998]"}, {"versioned_ensembl_gene_id":"ENSG00000217716.3","gene_symbol":"RPS10P3","gene_name":"ribosomal protein S10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158104","summary":null,"start":88016300,"end":88016793,"strand":1,"description":"ribosomal protein S10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23684]"}, {"versioned_ensembl_gene_id":"ENSG00000261578.1","gene_symbol":"AP003119.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":76800364,"end":76804555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229258.5","gene_symbol":"AL445488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":211829846,"end":211853703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248671.7","gene_symbol":"ALG1L9P","gene_name":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:NCBI gene;Acc:285407]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285407","summary":null,"start":71794363,"end":71818238,"strand":-1,"description":"asparagine-linked glycosylation 1-like 9, pseudogene [Source:NCBI gene;Acc:285407]"}, {"versioned_ensembl_gene_id":"ENSG00000213585.10","gene_symbol":"VDAC1","gene_name":"voltage dependent anion channel 1 [Source:HGNC Symbol;Acc:HGNC:12669]","synonyms":"PORIN,MGC111064","biotype":"protein_coding","ncbi_id":"7416","summary":"This gene encodes a voltage-dependent anion channel protein that is a major component of the outer mitochondrial membrane. The encoded protein facilitates the exchange of metabolites and ions across the outer mitochondrial membrane and may regulate mitochondrial functions. This protein also forms channels in the plasma membrane and may be involved in transmembrane electron transport. Alternate splicing results in multiple transcript variants. Multiple pseudogenes of this gene are found on chromosomes 1, 2 3, 6, 9, 12, X and Y.[provided by RefSeq, Sep 2010]","start":133971915,"end":134005133,"strand":-1,"description":"voltage dependent anion channel 1 [Source:HGNC Symbol;Acc:HGNC:12669]"}, {"versioned_ensembl_gene_id":"ENSG00000152254.10","gene_symbol":"G6PC2","gene_name":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]","synonyms":"IGRP","biotype":"protein_coding","ncbi_id":"57818","summary":"This gene encodes an enzyme belonging to the glucose-6-phosphatase catalytic subunit family. These enzymes are part of a multicomponent integral membrane system that catalyzes the hydrolysis of glucose-6-phosphate, the terminal step in gluconeogenic and glycogenolytic pathways, allowing the release of glucose into the bloodstream. The family member encoded by this gene is found in pancreatic islets and does not exhibit phosphohydrolase activity, but it is a major target of cell-mediated autoimmunity in diabetes. Several alternatively spliced transcript variants of this gene have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":168901240,"end":168910000,"strand":1,"description":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]"}, {"versioned_ensembl_gene_id":"ENSG00000223776.5","gene_symbol":"LGALS8-AS1","gene_name":"LGALS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40340]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287902","summary":null,"start":236523052,"end":236524508,"strand":-1,"description":"LGALS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40340]"}, {"versioned_ensembl_gene_id":"ENSG00000273058.2","gene_symbol":"AL359921.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":236536162,"end":236536704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269091.5","gene_symbol":"AC010624.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50043196,"end":50051062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183077.15","gene_symbol":"AFMID","gene_name":"arylformamidase [Source:HGNC Symbol;Acc:HGNC:20910]","synonyms":"DKFZp686F03259,KF","biotype":"protein_coding","ncbi_id":"125061","summary":null,"start":78187317,"end":78207701,"strand":1,"description":"arylformamidase [Source:HGNC Symbol;Acc:HGNC:20910]"}, {"versioned_ensembl_gene_id":"ENSG00000278311.4","gene_symbol":"GGNBP2","gene_name":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]","synonyms":"ZNF403,ZFP403,LZK1,FLJ22561,FLJ21230,DIF3,DIF-3","biotype":"protein_coding","ncbi_id":"79893","summary":null,"start":36544888,"end":36589848,"strand":1,"description":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]"}, {"versioned_ensembl_gene_id":"ENSG00000198873.11","gene_symbol":"GRK5","gene_name":"G protein-coupled receptor kinase 5 [Source:HGNC Symbol;Acc:HGNC:4544]","synonyms":"GPRK5","biotype":"protein_coding","ncbi_id":"2869","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. It has also been shown to play a role in regulating the motility of polymorphonuclear leukocytes (PMNs). [provided by RefSeq, Jul 2008]","start":119207589,"end":119459742,"strand":1,"description":"G protein-coupled receptor kinase 5 [Source:HGNC Symbol;Acc:HGNC:4544]"}, {"versioned_ensembl_gene_id":"ENSG00000268041.2","gene_symbol":"AC010616.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41907705,"end":41928516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271109.1","gene_symbol":"AC008555.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34849278,"end":34860576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269086.2","gene_symbol":"AC008555.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34837889,"end":34855304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229795.2","gene_symbol":"RPS21P1","gene_name":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271090","summary":null,"start":235432985,"end":235433231,"strand":1,"description":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]"}, {"versioned_ensembl_gene_id":"ENSG00000235495.1","gene_symbol":"AC007422.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67565604,"end":67684077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235718.8","gene_symbol":"MFRP","gene_name":"membrane frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:18121]","synonyms":"C1QTNF5,rd6,NNO2,FLJ30570","biotype":"protein_coding","ncbi_id":"83552","summary":"This gene encodes a member of the frizzled-related protein family. The encoded protein plays an important role in eye development and mutations in this gene have been associated with nanophthalmos, posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc drusen. The protein is encoded by a bicistronic transcript which also encodes C1q and tumor necrosis factor related protein 5 (C1QTNF5). [provided by RefSeq, Jun 2013]","start":119338942,"end":119346673,"strand":-1,"description":"membrane frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:18121]"}, {"versioned_ensembl_gene_id":"ENSG00000238259.1","gene_symbol":"AC067940.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168231921,"end":168232220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248736.1","gene_symbol":"AC112192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2965006,"end":2967628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248137.1","gene_symbol":"AC094105.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2831021,"end":2835139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219702.1","gene_symbol":"AL078599.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81764211,"end":81764503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232939.1","gene_symbol":"AL158829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109760360,"end":109772043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228053.1","gene_symbol":"AL158823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110024881,"end":110025358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258678.1","gene_symbol":"LINC02317","gene_name":"long intergenic non-protein coding RNA 2317 [Source:HGNC Symbol;Acc:HGNC:53236]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101930294","summary":null,"start":90452063,"end":90455117,"strand":-1,"description":"long intergenic non-protein coding RNA 2317 [Source:HGNC Symbol;Acc:HGNC:53236]"}, {"versioned_ensembl_gene_id":"ENSG00000179820.15","gene_symbol":"MYADM","gene_name":"myeloid associated differentiation marker [Source:HGNC Symbol;Acc:HGNC:7544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91663","summary":null,"start":53866223,"end":53876437,"strand":1,"description":"myeloid associated differentiation marker [Source:HGNC Symbol;Acc:HGNC:7544]"}, {"versioned_ensembl_gene_id":"ENSG00000150316.11","gene_symbol":"CWC15","gene_name":"CWC15 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:26939]","synonyms":"HSPC148,Cwf15,C11orf5,AD002","biotype":"protein_coding","ncbi_id":"51503","summary":null,"start":94962622,"end":94973612,"strand":-1,"description":"CWC15 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:26939]"}, {"versioned_ensembl_gene_id":"ENSG00000255774.1","gene_symbol":"AP000439.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69477133,"end":69479940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255606.1","gene_symbol":"AP000439.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69438365,"end":69444743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259133.5","gene_symbol":"AL161757.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56648965,"end":56730535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253600.1","gene_symbol":"AC008446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164601002,"end":164601452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273777.4","gene_symbol":"CEACAM20","gene_name":"carcinoembryonic antigen related cell adhesion molecule 20 [Source:HGNC Symbol;Acc:HGNC:24879]","synonyms":"UNQ9366","biotype":"protein_coding","ncbi_id":"125931","summary":null,"start":44501677,"end":44529788,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 20 [Source:HGNC Symbol;Acc:HGNC:24879]"}, {"versioned_ensembl_gene_id":"ENSG00000119720.17","gene_symbol":"NRDE2","gene_name":"NRDE-2, necessary for RNA interference, domain containing [Source:HGNC Symbol;Acc:HGNC:20186]","synonyms":"FLJ14051,C14orf102","biotype":"protein_coding","ncbi_id":"55051","summary":null,"start":90267856,"end":90332137,"strand":-1,"description":"NRDE-2, necessary for RNA interference, domain containing [Source:HGNC Symbol;Acc:HGNC:20186]"}, {"versioned_ensembl_gene_id":"ENSG00000056558.10","gene_symbol":"TRAF1","gene_name":"TNF receptor associated factor 1 [Source:HGNC Symbol;Acc:HGNC:12031]","synonyms":"EBI6","biotype":"protein_coding","ncbi_id":"7185","summary":"The protein encoded by this gene is a member of the TNF receptor (TNFR) associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from various receptors of the TNFR superfamily. This protein and TRAF2 form a heterodimeric complex, which is required for TNF-alpha-mediated activation of MAPK8/JNK and NF-kappaB. The protein complex formed by this protein and TRAF2 also interacts with inhibitor-of-apoptosis proteins (IAPs), and thus mediates the anti-apoptotic signals from TNF receptors. The expression of this protein can be induced by Epstein-Barr virus (EBV). EBV infection membrane protein 1 (LMP1) is found to interact with this and other TRAF proteins; this interaction is thought to link LMP1-mediated B lymphocyte transformation to the signal transduction from TNFR family receptors. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":120902393,"end":120929173,"strand":-1,"description":"TNF receptor associated factor 1 [Source:HGNC Symbol;Acc:HGNC:12031]"}, {"versioned_ensembl_gene_id":"ENSG00000270506.1","gene_symbol":"AC021646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93035261,"end":93035744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257746.1","gene_symbol":"AC138123.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93090522,"end":93107600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258171.1","gene_symbol":"LINC02412","gene_name":"long intergenic non-protein coding RNA 2412 [Source:HGNC Symbol;Acc:HGNC:53341]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724933","summary":null,"start":93174366,"end":93181832,"strand":1,"description":"long intergenic non-protein coding RNA 2412 [Source:HGNC Symbol;Acc:HGNC:53341]"}, {"versioned_ensembl_gene_id":"ENSG00000172927.7","gene_symbol":"MYEOV","gene_name":"myeloma overexpressed [Source:HGNC Symbol;Acc:HGNC:7563]","synonyms":"OCIM","biotype":"protein_coding","ncbi_id":"26579","summary":null,"start":69294138,"end":69367726,"strand":1,"description":"myeloma overexpressed [Source:HGNC Symbol;Acc:HGNC:7563]"}, {"versioned_ensembl_gene_id":"ENSG00000249842.1","gene_symbol":"AC010486.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85446974,"end":85447758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213275.2","gene_symbol":"IFITM9P","gene_name":"interferon induced transmembrane protein 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33972]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390218","summary":null,"start":69303412,"end":69303807,"strand":-1,"description":"interferon induced transmembrane protein 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33972]"}, {"versioned_ensembl_gene_id":"ENSG00000249023.1","gene_symbol":"AC010486.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85429702,"end":85430184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236900.1","gene_symbol":"TIMM9P1","gene_name":"TIMM9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862726","summary":null,"start":74344550,"end":74344805,"strand":-1,"description":"TIMM9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39928]"}, {"versioned_ensembl_gene_id":"ENSG00000256469.1","gene_symbol":"AP002383.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94874052,"end":94925521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204427.11","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"BAT5,NG26,D6S82E","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31686949,"end":31703444,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000279222.1","gene_symbol":"AC025183.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1858409,"end":1859890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250417.1","gene_symbol":"LINC02116","gene_name":"long intergenic non-protein coding RNA 2116 [Source:HGNC Symbol;Acc:HGNC:52971]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929034","summary":null,"start":1855970,"end":1856568,"strand":-1,"description":"long intergenic non-protein coding RNA 2116 [Source:HGNC Symbol;Acc:HGNC:52971]"}, {"versioned_ensembl_gene_id":"ENSG00000156110.13","gene_symbol":"ADK","gene_name":"adenosine kinase [Source:HGNC Symbol;Acc:HGNC:257]","synonyms":"AK","biotype":"protein_coding","ncbi_id":"132","summary":"This gene an enzyme which catalyzes the transfer of the gamma-phosphate from ATP to adenosine, thereby serving as a regulator of concentrations of both extracellular adenosine and intracellular adenine nucleotides. Adenosine has widespread effects on the cardiovascular, nervous, respiratory, and immune systems and inhibitors of the enzyme could play an important pharmacological role in increasing intravascular adenosine concentrations and acting as anti-inflammatory agents. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":74151185,"end":74709303,"strand":1,"description":"adenosine kinase [Source:HGNC Symbol;Acc:HGNC:257]"}, {"versioned_ensembl_gene_id":"ENSG00000264940.4","gene_symbol":"SNORD3C","gene_name":"small nucleolar RNA, C/D box 3C [Source:HGNC Symbol;Acc:HGNC:33191]","synonyms":"U3-3,RNU3-3","biotype":"snoRNA","ncbi_id":"780853","summary":null,"start":19189665,"end":19190245,"strand":-1,"description":"small nucleolar RNA, C/D box 3C [Source:HGNC Symbol;Acc:HGNC:33191]"}, {"versioned_ensembl_gene_id":"ENSG00000273755.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713341,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000196371.3","gene_symbol":"FUT4","gene_name":"fucosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4015]","synonyms":"FUC-TIV,FCT3A,ELFT,CD15","biotype":"protein_coding","ncbi_id":"2526","summary":"The product of this gene transfers fucose to N-acetyllactosamine polysaccharides to generate fucosylated carbohydrate structures. It catalyzes the synthesis of the non-sialylated antigen, Lewis x (CD15). [provided by RefSeq, Jan 2009]","start":94543840,"end":94549898,"strand":1,"description":"fucosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4015]"}, {"versioned_ensembl_gene_id":"ENSG00000217231.2","gene_symbol":"AL109755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144036618,"end":144037704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254134.1","gene_symbol":"IGHVII-74-1","gene_name":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]","synonyms":"IGHV(II)-74-1","biotype":"IG_V_pseudogene","ncbi_id":"28357","summary":null,"start":106821174,"end":106821414,"strand":-1,"description":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]"}, {"versioned_ensembl_gene_id":"ENSG00000270419.1","gene_symbol":"CAHM","gene_name":"colon adenocarcinoma hypermethylated (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:42860]","synonyms":"LINC00468","biotype":"lincRNA","ncbi_id":"100526820","summary":null,"start":163413065,"end":163413960,"strand":-1,"description":"colon adenocarcinoma hypermethylated (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:42860]"}, {"versioned_ensembl_gene_id":"ENSG00000231635.1","gene_symbol":"ATP5BP1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:831]","synonyms":"ATPSBL1,ATPMBL1,ATP5BL1","biotype":"processed_pseudogene","ncbi_id":"507","summary":null,"start":98206151,"end":98207724,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:831]"}, {"versioned_ensembl_gene_id":"ENSG00000269877.3","gene_symbol":"AC008753.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53787597,"end":53788169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259868.2","gene_symbol":"AL163952.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55896547,"end":55962970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280411.1","gene_symbol":"AC245369.3","gene_name":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106762092,"end":106762588,"strand":-1,"description":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]"}, {"versioned_ensembl_gene_id":"ENSG00000272386.1","gene_symbol":"AC015802.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":76551352,"end":76551750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011347.9","gene_symbol":"SYT7","gene_name":"synaptotagmin 7 [Source:HGNC Symbol;Acc:HGNC:11514]","synonyms":"SYT-VII,PCANAP7,MGC150517,IPCA-7","biotype":"protein_coding","ncbi_id":"9066","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. A similar protein in rodents mediates hormone secretion and lysosome exocytosis. In humans, expression of this gene has been associated with prostate cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":61515313,"end":61581148,"strand":-1,"description":"synaptotagmin 7 [Source:HGNC Symbol;Acc:HGNC:11514]"}, {"versioned_ensembl_gene_id":"ENSG00000230321.1","gene_symbol":"MTCO2P27","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52156]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075291","summary":null,"start":12504905,"end":12505976,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52156]"}, {"versioned_ensembl_gene_id":"ENSG00000137492.7","gene_symbol":"THAP12","gene_name":"THAP domain containing 12 [Source:HGNC Symbol;Acc:HGNC:9440]","synonyms":"THAP0,PRKRIR,P52rIPK,DAP4","biotype":"protein_coding","ncbi_id":"5612","summary":null,"start":76349956,"end":76380971,"strand":-1,"description":"THAP domain containing 12 [Source:HGNC Symbol;Acc:HGNC:9440]"}, {"versioned_ensembl_gene_id":"ENSG00000189152.10","gene_symbol":"GRAPL","gene_name":"GRB2 related adaptor protein like [Source:HGNC Symbol;Acc:HGNC:37240]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400581","summary":null,"start":19127469,"end":19159176,"strand":1,"description":"GRB2 related adaptor protein like [Source:HGNC Symbol;Acc:HGNC:37240]"}, {"versioned_ensembl_gene_id":"ENSG00000005102.12","gene_symbol":"MEOX1","gene_name":"mesenchyme homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7013]","synonyms":"MOX1","biotype":"protein_coding","ncbi_id":"4222","summary":"This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":43640388,"end":43661954,"strand":-1,"description":"mesenchyme homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7013]"}, {"versioned_ensembl_gene_id":"ENSG00000062370.16","gene_symbol":"ZNF112","gene_name":"zinc finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12892]","synonyms":"ZNF228,ZFP112","biotype":"protein_coding","ncbi_id":"7771","summary":null,"start":44326555,"end":44367217,"strand":-1,"description":"zinc finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12892]"}, {"versioned_ensembl_gene_id":"ENSG00000129673.9","gene_symbol":"AANAT","gene_name":"aralkylamine N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:19]","synonyms":"SNAT","biotype":"protein_coding","ncbi_id":"15","summary":"The protein encoded by this gene belongs to the acetyltransferase superfamily. It is the penultimate enzyme in melatonin synthesis and controls the night/day rhythm in melatonin production in the vertebrate pineal gland. Melatonin is essential for the function of the circadian clock that influences activity and sleep. This enzyme is regulated by cAMP-dependent phosphorylation that promotes its interaction with 14-3-3 proteins and thus protects the enzyme against proteasomal degradation. This gene may contribute to numerous genetic diseases such as delayed sleep phase syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":76453351,"end":76470117,"strand":1,"description":"aralkylamine N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:19]"}, {"versioned_ensembl_gene_id":"ENSG00000268994.3","gene_symbol":"FAM236B","gene_name":"family with sequence similarity 236 member B [Source:HGNC Symbol;Acc:HGNC:52640]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132304","summary":null,"start":72781865,"end":72782660,"strand":-1,"description":"family with sequence similarity 236 member B [Source:HGNC Symbol;Acc:HGNC:52640]"}, {"versioned_ensembl_gene_id":"ENSG00000241537.1","gene_symbol":"AC134050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72772539,"end":72773471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187621.14","gene_symbol":"TCL6","gene_name":"T-cell leukemia/lymphoma 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13463]","synonyms":"TNG2,TNG1,TCL6e1","biotype":"processed_transcript","ncbi_id":"27004","summary":null,"start":95650498,"end":95679833,"strand":1,"description":"T-cell leukemia/lymphoma 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13463]"}, {"versioned_ensembl_gene_id":"ENSG00000227217.1","gene_symbol":"AL356276.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157691762,"end":157696459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258661.1","gene_symbol":"AL079303.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36647083,"end":36658801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129250.11","gene_symbol":"KIF1C","gene_name":"kinesin family member 1C [Source:HGNC Symbol;Acc:HGNC:6317]","synonyms":"SPAX2,SAX2,SPG58","biotype":"protein_coding","ncbi_id":"10749","summary":"The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]","start":4997948,"end":5028401,"strand":1,"description":"kinesin family member 1C [Source:HGNC Symbol;Acc:HGNC:6317]"}, {"versioned_ensembl_gene_id":"ENSG00000227495.1","gene_symbol":"AC004771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5019214,"end":5020093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258708.1","gene_symbol":"SLC25A21-AS1","gene_name":"SLC25A21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44298]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129794","summary":null,"start":37171888,"end":37173811,"strand":1,"description":"SLC25A21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44298]"}, {"versioned_ensembl_gene_id":"ENSG00000230104.1","gene_symbol":"AC018712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172674212,"end":172674898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248126.1","gene_symbol":"AC091849.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1598127,"end":1598247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230769.1","gene_symbol":"Z98048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40788777,"end":40789267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085552.16","gene_symbol":"IGSF9","gene_name":"immunoglobulin superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:18132]","synonyms":"Nrt1,KIAA1355,IGSF9A","biotype":"protein_coding","ncbi_id":"57549","summary":null,"start":159927039,"end":159945604,"strand":-1,"description":"immunoglobulin superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:18132]"}, {"versioned_ensembl_gene_id":"ENSG00000253742.1","gene_symbol":"IGHV3-60","gene_name":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28417","summary":null,"start":106631197,"end":106631653,"strand":-1,"description":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]"}, {"versioned_ensembl_gene_id":"ENSG00000236783.1","gene_symbol":"RPS15AP27","gene_name":"ribosomal protein S15a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271613","summary":null,"start":107963703,"end":107964045,"strand":-1,"description":"ribosomal protein S15a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37011]"}, {"versioned_ensembl_gene_id":"ENSG00000260097.2","gene_symbol":"SPDYE6","gene_name":"speedy/RINGO cell cycle regulator family member E6 [Source:HGNC Symbol;Acc:HGNC:35465]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729597","summary":"This gene encodes a cell cycle regulatory protein which plays an important role in cell cycle progression by binding and activating cyclin-dependent kinases. The encoded protein belongs to a family of cyclin-dependent kinase regulators that contain a speedy box domain which is required for cyclin-dependent kinase activation. [provided by RefSeq, Jul 2017]","start":102347206,"end":102356444,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E6 [Source:HGNC Symbol;Acc:HGNC:35465]"}, {"versioned_ensembl_gene_id":"ENSG00000143951.15","gene_symbol":"WDPCP","gene_name":"WD repeat containing planar cell polarity effector [Source:HGNC Symbol;Acc:HGNC:28027]","synonyms":"hFrtz,fritz,C2orf86,BBS15","biotype":"protein_coding","ncbi_id":"51057","summary":"This gene encodes a cytoplasmic WD40 repeat protein. A similar gene in frogs encodes a planar cell polarity protein that plays a critical role in collective cell movement and ciliogenesis by mediating septin localization. Mutations in this gene are associated with Bardet-Biedl syndrome 15 and may also play a role in Meckel-Gruber syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":63121383,"end":63827843,"strand":-1,"description":"WD repeat containing planar cell polarity effector [Source:HGNC Symbol;Acc:HGNC:28027]"}, {"versioned_ensembl_gene_id":"ENSG00000249693.2","gene_symbol":"THEGL","gene_name":"theg spermatid protein like [Source:HGNC Symbol;Acc:HGNC:43771]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506564","summary":null,"start":56530609,"end":56603507,"strand":1,"description":"theg spermatid protein like [Source:HGNC Symbol;Acc:HGNC:43771]"}, {"versioned_ensembl_gene_id":"ENSG00000253808.1","gene_symbol":"IGHVII-46-1","gene_name":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]","synonyms":"IGHV(II)-46-1","biotype":"IG_V_pseudogene","ncbi_id":"28365","summary":null,"start":106515818,"end":106515854,"strand":-1,"description":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]"}, {"versioned_ensembl_gene_id":"ENSG00000177556.11","gene_symbol":"ATOX1","gene_name":"antioxidant 1 copper chaperone [Source:HGNC Symbol;Acc:HGNC:798]","synonyms":"HAH1","biotype":"protein_coding","ncbi_id":"475","summary":"This gene encodes a copper chaperone that plays a role in copper homeostasis by binding and transporting cytosolic copper to ATPase proteins in the trans-Golgi network for later incorporation to the ceruloplasmin. This protein also functions as an antioxidant against superoxide and hydrogen peroxide, and therefore, may play a significant role in cancer carcinogenesis. Because of its cytogenetic location, this gene represents a candidate gene for 5q-syndrome. [provided by RefSeq, Jul 2008]","start":151742316,"end":151772532,"strand":-1,"description":"antioxidant 1 copper chaperone [Source:HGNC Symbol;Acc:HGNC:798]"}, {"versioned_ensembl_gene_id":"ENSG00000279908.1","gene_symbol":"AC026748.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1383159,"end":1386409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150403.17","gene_symbol":"TMCO3","gene_name":"transmembrane and coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:20329]","synonyms":"FLJ20623,C13orf11","biotype":"protein_coding","ncbi_id":"55002","summary":"This gene encodes a member of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Members of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular membranes. Mutations in this gene have been identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract. [provided by RefSeq, Mar 2017]","start":113490995,"end":113554590,"strand":1,"description":"transmembrane and coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:20329]"}, {"versioned_ensembl_gene_id":"ENSG00000095321.16","gene_symbol":"CRAT","gene_name":"carnitine O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2342]","synonyms":"CAT1","biotype":"protein_coding","ncbi_id":"1384","summary":"This gene encodes carnitine O-acetyltransferase, a member of the carnitine acyltransferase family and a key metabolic pathway enzyme which plays an important role in energy homeostasis and fat metabolism. This enzyme catalyzes the reversible transfer of acyl groups from an acyl-CoA thioester to carnitine and regulates the ratio of acyl-CoA/CoA. It is found in both the mitochondria and the peroxisome. Alternative splicing results in transcript variants encoding different isoforms that may localize to different subcellular compartments. [provided by RefSeq, Oct 2016]","start":129094810,"end":129111189,"strand":-1,"description":"carnitine O-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:2342]"}, {"versioned_ensembl_gene_id":"ENSG00000234055.1","gene_symbol":"AL158151.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129097854,"end":129100266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143473.12","gene_symbol":"KCNH1","gene_name":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]","synonyms":"Kv10.1,h-eag,eag1,eag","biotype":"protein_coding","ncbi_id":"3756","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit of a voltage-gated non-inactivating delayed rectifier potassium channel. It is activated at the onset of myoblast differentiation. The gene is highly expressed in brain and in myoblasts. Overexpression of the gene may confer a growth advantage to cancer cells and favor tumor cell proliferation. Alternative splicing of this gene results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":210676823,"end":211134180,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]"}, {"versioned_ensembl_gene_id":"ENSG00000249400.1","gene_symbol":"HMGB3P17","gene_name":"high mobility group box 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39309]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419948","summary":null,"start":123468781,"end":123469429,"strand":-1,"description":"high mobility group box 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39309]"}, {"versioned_ensembl_gene_id":"ENSG00000255083.2","gene_symbol":"OR5AK1P","gene_name":"olfactory receptor family 5 subfamily AK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15250]","synonyms":"OR5AK5P","biotype":"unprocessed_pseudogene","ncbi_id":"81230","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57018100,"end":57019021,"strand":1,"description":"olfactory receptor family 5 subfamily AK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15250]"}, {"versioned_ensembl_gene_id":"ENSG00000229737.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"BPG126D10.10,OTTHUMG00000086663","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577378,"end":29577667,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000255293.1","gene_symbol":"WIZP1","gene_name":"widely interspaced zinc finger motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645598","summary":null,"start":23403805,"end":23406103,"strand":1,"description":"widely interspaced zinc finger motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51696]"}, {"versioned_ensembl_gene_id":"ENSG00000271491.1","gene_symbol":"AC100767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23370116,"end":23377644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231871.5","gene_symbol":"IPO9-AS1","gene_name":"IPO9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40892]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873949","summary":null,"start":201688259,"end":201829559,"strand":-1,"description":"IPO9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40892]"}, {"versioned_ensembl_gene_id":"ENSG00000241701.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30223924,"end":30315930,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000254768.5","gene_symbol":"AC104009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22283730,"end":22338245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253915.1","gene_symbol":"AC104371.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135625185,"end":135625981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228547.5","gene_symbol":"OR7E26P","gene_name":"olfactory receptor family 7 subfamily E member 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:8398]","synonyms":"OR912-95,OR7E70P,OR7E69P,OR7E68P,OR7E67P,OR1-73,OR1-72,OR1-51","biotype":"unprocessed_pseudogene","ncbi_id":"401637","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14999050,"end":15000055,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 26 pseudogene [Source:HGNC Symbol;Acc:HGNC:8398]"}, {"versioned_ensembl_gene_id":"ENSG00000278797.1","gene_symbol":"AC011551.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46533669,"end":46534351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254203.1","gene_symbol":"IGHVII-33-1","gene_name":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]","synonyms":"IGHV(II)-33-1","biotype":"IG_V_pseudogene","ncbi_id":"28369","summary":null,"start":106367385,"end":106367664,"strand":-1,"description":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]"}, {"versioned_ensembl_gene_id":"ENSG00000211955.2","gene_symbol":"IGHV3-33","gene_name":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28434","summary":null,"start":106359793,"end":106360324,"strand":-1,"description":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]"}, {"versioned_ensembl_gene_id":"ENSG00000270474.2","gene_symbol":"IGHV3-29","gene_name":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28440","summary":null,"start":106356145,"end":106356591,"strand":-1,"description":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]"}, {"versioned_ensembl_gene_id":"ENSG00000233613.5","gene_symbol":"DCUN1D2-AS","gene_name":"DCUN1D2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:39889]","synonyms":"DCUN1D2-AS2","biotype":"antisense_RNA","ncbi_id":"100874229","summary":null,"start":113468901,"end":113476135,"strand":1,"description":"DCUN1D2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:39889]"}, {"versioned_ensembl_gene_id":"ENSG00000224566.2","gene_symbol":"FAM96AP2","gene_name":"family with sequence similarity 96 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391174","summary":null,"start":228114997,"end":228115473,"strand":-1,"description":"family with sequence similarity 96 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43862]"}, {"versioned_ensembl_gene_id":"ENSG00000249992.1","gene_symbol":"TMEM158","gene_name":"transmembrane protein 158 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30293]","synonyms":"RIS1,p40BBp","biotype":"protein_coding","ncbi_id":"25907","summary":"Constitutive activation of the Ras pathway triggers an irreversible proliferation arrest reminiscent of replicative senescence. Transcription of this gene is upregulated in response to activation of the Ras pathway, but not under other conditions that induce senescence. The encoded protein is similar to a rat cell surface receptor proposed to function in a neuronal survival pathway. An allelic polymorphism in this gene results in both functional and non-functional (frameshifted) alleles; the reference genome represents the functional allele. [provided by RefSeq, Jul 2015]","start":45224466,"end":45226278,"strand":-1,"description":"transmembrane protein 158 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30293]"}, {"versioned_ensembl_gene_id":"ENSG00000233314.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30059208,"end":30062832,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000224094.1","gene_symbol":"RPS24P8","gene_name":"ribosomal protein S24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216336","summary":null,"start":45159774,"end":45160175,"strand":-1,"description":"ribosomal protein S24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37016]"}, {"versioned_ensembl_gene_id":"ENSG00000257949.6","gene_symbol":"TEN1","gene_name":"TEN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:37242]","synonyms":"FLJ39785,C17orf106","biotype":"protein_coding","ncbi_id":"100134934","summary":"C17ORF106, or TEN1, appears to function in a telomere-associated complex with STN1 (OBFC1; MIM 613128) and CTC1 (C17ORF68; MIM 613129) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009]","start":75979220,"end":76000586,"strand":1,"description":"TEN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:37242]"}, {"versioned_ensembl_gene_id":"ENSG00000276210.2","gene_symbol":"LINC00226","gene_name":"long intergenic non-protein coding RNA 226 [Source:HGNC Symbol;Acc:HGNC:20168]","synonyms":"C14orf97,NCRNA00226","biotype":"lincRNA","ncbi_id":"338004","summary":null,"start":106287674,"end":106288828,"strand":1,"description":"long intergenic non-protein coding RNA 226 [Source:HGNC Symbol;Acc:HGNC:20168]"}, {"versioned_ensembl_gene_id":"ENSG00000204950.3","gene_symbol":"LRRC10B","gene_name":"leucine rich repeat containing 10B [Source:HGNC Symbol;Acc:HGNC:37215]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390205","summary":null,"start":61508800,"end":61511018,"strand":1,"description":"leucine rich repeat containing 10B [Source:HGNC Symbol;Acc:HGNC:37215]"}, {"versioned_ensembl_gene_id":"ENSG00000204338.8","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21A,P450c21A,CYP21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":32005636,"end":32008451,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000215424.9","gene_symbol":"MCM3AP-AS1","gene_name":"MCM3AP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16417]","synonyms":"NCRNA00031,MCM3APAS,MCM3AP-AS,FLJ10508,C21orf85","biotype":"antisense_RNA","ncbi_id":"114044","summary":null,"start":46229217,"end":46259390,"strand":1,"description":"MCM3AP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16417]"}, {"versioned_ensembl_gene_id":"ENSG00000228137.1","gene_symbol":"AP001469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46246890,"end":46247682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226984.1","gene_symbol":"AL035410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114459934,"end":114460360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154025.15","gene_symbol":"SLC5A10","gene_name":"solute carrier family 5 member 10 [Source:HGNC Symbol;Acc:HGNC:23155]","synonyms":"SGLT5","biotype":"protein_coding","ncbi_id":"125206","summary":"This gene is a member of the sodium/glucose transporter family. Members of this family are sodium-dependent transporters and can be divided into two subfamilies based on sequence homology, one that co-transports sugars and the second that transports molecules such as ascorbate, choline, iodide, lipoate, monocaroboxylates, and pantothenate. The protein encoded by this gene has the highest affinity for mannose and has been reported to be most highly expressed in the kidney. This protein may function as a kidney-specific, sodium-dependent mannose and fructose co-transporter. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":18950345,"end":19022595,"strand":1,"description":"solute carrier family 5 member 10 [Source:HGNC Symbol;Acc:HGNC:23155]"}, {"versioned_ensembl_gene_id":"ENSG00000230603.1","gene_symbol":"AC011753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109665209,"end":109665742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225975.6","gene_symbol":"LINC01534","gene_name":"long intergenic non-protein coding RNA 1534 [Source:HGNC Symbol;Acc:HGNC:51281]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927621","summary":null,"start":36685440,"end":36687449,"strand":-1,"description":"long intergenic non-protein coding RNA 1534 [Source:HGNC Symbol;Acc:HGNC:51281]"}, {"versioned_ensembl_gene_id":"ENSG00000086758.15","gene_symbol":"HUWE1","gene_name":"HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:30892]","synonyms":"UREB1,KIAA0312,Ib772","biotype":"protein_coding","ncbi_id":"10075","summary":"This gene encodes a protein containing a C-terminal HECT (E6AP type E3 ubiquitin protein ligase) domain that functions as an E3 ubiquitin ligase. The encoded protein is required for the ubiquitination and subsequent degradation of the anti-apoptotic protein Mcl1 (myeloid cell leukemia sequence 1 (BCL2-related)). This protein also ubiquitinates the p53 tumor suppressor, core histones, and DNA polymerase beta. Mutations in this gene are associated with Turner type X-linked syndromic cognitive disability. [provided by RefSeq, Aug 2013]","start":53532096,"end":53686729,"strand":-1,"description":"HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:30892]"}, {"versioned_ensembl_gene_id":"ENSG00000101986.11","gene_symbol":"ABCD1","gene_name":"ATP binding cassette subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:61]","synonyms":"AMN,ALDP,ALD,adrenoleukodystrophy","biotype":"protein_coding","ncbi_id":"215","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system. [provided by RefSeq, Jul 2008]","start":153724868,"end":153744762,"strand":1,"description":"ATP binding cassette subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:61]"}, {"versioned_ensembl_gene_id":"ENSG00000276070.4","gene_symbol":"CCL4L2","gene_name":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9560","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this family member is similar to the chemokine (C-C motif) ligand 4 product, which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals, where most individuals have one to five copies. This gene copy contains a non-consensus splice acceptor site at the 3' terminal exon found in other highly similar gene copies, and it thus uses other alternative splice sites for the 3' terminal exon, resulting in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36210924,"end":36212878,"strand":1,"description":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]"}, {"versioned_ensembl_gene_id":"ENSG00000119328.11","gene_symbol":"FAM206A","gene_name":"family with sequence similarity 206 member A [Source:HGNC Symbol;Acc:HGNC:1364]","synonyms":"C9orf6,Simiate,FLJ20457,CG-8","biotype":"protein_coding","ncbi_id":"54942","summary":null,"start":108934181,"end":108950744,"strand":1,"description":"family with sequence similarity 206 member A [Source:HGNC Symbol;Acc:HGNC:1364]"}, {"versioned_ensembl_gene_id":"ENSG00000122861.15","gene_symbol":"PLAU","gene_name":"plasminogen activator, urokinase [Source:HGNC Symbol;Acc:HGNC:9052]","synonyms":"UPA,URK","biotype":"protein_coding","ncbi_id":"5328","summary":"This gene encodes a secreted serine protease that converts plasminogen to plasmin. The encoded preproprotein is proteolytically processed to generate A and B polypeptide chains. These chains associate via a single disulfide bond to form the catalytically inactive high molecular weight urokinase-type plasminogen activator (HMW-uPA). HMW-uPA can be further processed into the catalytically active low molecular weight urokinase-type plasminogen activator (LMW-uPA). This low molecular weight form does not bind to the urokinase-type plasminogen activator receptor. Mutations in this gene may be associated with Quebec platelet disorder and late-onset Alzheimer's disease. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":73909177,"end":73917497,"strand":1,"description":"plasminogen activator, urokinase [Source:HGNC Symbol;Acc:HGNC:9052]"}, {"versioned_ensembl_gene_id":"ENSG00000255428.1","gene_symbol":"AP002008.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":111414242,"end":111418186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250706.1","gene_symbol":"AC079340.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152146385,"end":152178573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274572.1","gene_symbol":"ZYXP1","gene_name":"zyxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51695]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480342","summary":null,"start":137424904,"end":137425021,"strand":-1,"description":"zyxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51695]"}, {"versioned_ensembl_gene_id":"ENSG00000253879.1","gene_symbol":"AC087664.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59601378,"end":59613775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204152.10","gene_symbol":"TIMM23B","gene_name":"translocase of inner mitochondrial membrane 23 homolog B [Source:HGNC Symbol;Acc:HGNC:23581]","synonyms":"bA592B15.7","biotype":"protein_coding","ncbi_id":"100652748","summary":null,"start":49942033,"end":49974850,"strand":1,"description":"translocase of inner mitochondrial membrane 23 homolog B [Source:HGNC Symbol;Acc:HGNC:23581]"}, {"versioned_ensembl_gene_id":"ENSG00000253883.1","gene_symbol":"IGHV3-19","gene_name":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28446","summary":null,"start":106196700,"end":106196990,"strand":-1,"description":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]"}, {"versioned_ensembl_gene_id":"ENSG00000211945.2","gene_symbol":"IGHV1-18","gene_name":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28468","summary":null,"start":106184901,"end":106185394,"strand":-1,"description":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]"}, {"versioned_ensembl_gene_id":"ENSG00000148343.18","gene_symbol":"MIGA2","gene_name":"mitoguardin 2 [Source:HGNC Symbol;Acc:HGNC:23621]","synonyms":"FLJ14596,FLJ00199,FAM73B,C9orf54","biotype":"protein_coding","ncbi_id":"84895","summary":null,"start":129036621,"end":129072082,"strand":1,"description":"mitoguardin 2 [Source:HGNC Symbol;Acc:HGNC:23621]"}, {"versioned_ensembl_gene_id":"ENSG00000235594.1","gene_symbol":"AL139824.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56267872,"end":56269231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242706.2","gene_symbol":"RPS27AP9","gene_name":"ribosomal protein S27a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271376","summary":null,"start":80498534,"end":80498971,"strand":-1,"description":"ribosomal protein S27a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35630]"}, {"versioned_ensembl_gene_id":"ENSG00000226389.3","gene_symbol":"MAPK6PS6","gene_name":"mitogen-activated protein kinase 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"282967","summary":null,"start":49771841,"end":49773299,"strand":1,"description":"mitogen-activated protein kinase 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18978]"}, {"versioned_ensembl_gene_id":"ENSG00000204856.11","gene_symbol":"FAM216A","gene_name":"family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]","synonyms":"HSU79274,C12orf24","biotype":"protein_coding","ncbi_id":"29902","summary":null,"start":110468364,"end":110490385,"strand":1,"description":"family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]"}, {"versioned_ensembl_gene_id":"ENSG00000103365.15","gene_symbol":"GGA2","gene_name":"golgi associated, gamma adaptin ear containing, ARF binding protein 2 [Source:HGNC Symbol;Acc:HGNC:16064]","synonyms":"VEAR,KIAA1080","biotype":"protein_coding","ncbi_id":"23062","summary":"This gene encodes a member of the Golgi-localized, gamma adaptin ear-containing, ARF-binding (GGA) family. This family includes ubiquitous coat proteins that regulate the trafficking of proteins between the trans-Golgi network and the lysosome. These proteins share an amino-terminal VHS domain which mediates sorting of the mannose 6-phosphate receptors at the trans-Golgi network. They also contain a carboxy-terminal region with homology to the ear domain of gamma-adaptins. This family member may play a significant role in cargo molecules regulation and clathrin-coated vesicle assembly. [provided by RefSeq, Jul 2008]","start":23463542,"end":23521995,"strand":-1,"description":"golgi associated, gamma adaptin ear containing, ARF binding protein 2 [Source:HGNC Symbol;Acc:HGNC:16064]"}, {"versioned_ensembl_gene_id":"ENSG00000197444.9","gene_symbol":"OGDHL","gene_name":"oxoglutarate dehydrogenase like [Source:HGNC Symbol;Acc:HGNC:25590]","synonyms":"FLJ10851","biotype":"protein_coding","ncbi_id":"55753","summary":"The protein encoded by this gene is similar to oxoglutarate dehydrogenase (OGDH) of the OGDH complex, which degrades glucose and glutamate. This gene encodes several isoforms, including some that appear to localize to mitochondria. The encoded protein down-regulates the AKT signaling cascade and can suppress the growth of cervical cancer cells. [provided by RefSeq, Dec 2016]","start":49734643,"end":49762379,"strand":-1,"description":"oxoglutarate dehydrogenase like [Source:HGNC Symbol;Acc:HGNC:25590]"}, {"versioned_ensembl_gene_id":"ENSG00000270890.1","gene_symbol":"AL049844.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143858062,"end":143858689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229529.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"HLA-75,dJ377H14.4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29788968,"end":29795307,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000274259.2","gene_symbol":"AL662799.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33437363,"end":33454453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099869.7","gene_symbol":"IGF2-AS","gene_name":"IGF2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:14062]","synonyms":"PEG8,IGF2AS,IGF2-AS1","biotype":"antisense_RNA","ncbi_id":"51214","summary":"This gene is expressed in antisense to the insulin-like growth factor 2 (IGF2) gene and is imprinted and paternally expressed. It is thought to be non-coding because the putative protein is not conserved and translation is predicted to trigger nonsense mediated decay (NMD). Transcripts from this gene are produced in tumors and may function to suppress cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":2140501,"end":2148666,"strand":1,"description":"IGF2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:14062]"}, {"versioned_ensembl_gene_id":"ENSG00000251627.1","gene_symbol":"AC010395.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110983563,"end":110984466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110245.11","gene_symbol":"APOC3","gene_name":"apolipoprotein C3 [Source:HGNC Symbol;Acc:HGNC:610]","synonyms":null,"biotype":"protein_coding","ncbi_id":"345","summary":"This gene encodes a protein component of triglyceride (TG)-rich lipoproteins (TRLs) including very low density lipoproteins (VLDL), high density lipoproteins (HDL) and chylomicrons. The encoded protein plays a role in role in the metabolism of these TRLs through multiple modes. This protein has been shown to promote the secretion of VLDL1, inhibit lipoprotein lipase enzyme activity, and delay catabolism of TRL remnants. Mutations in this gene are associated with low plasma triglyceride levels and reduced risk of ischemic cardiovascular disease, and hyperalphalipoproteinemia, which is characterized by elevated levels of high density lipoprotein (HDL) and HDL cholesterol in human patients. This gene and other related genes comprise an apolipoprotein gene cluster on chromosome 11. [provided by RefSeq, Sep 2017]","start":116829706,"end":116833072,"strand":1,"description":"apolipoprotein C3 [Source:HGNC Symbol;Acc:HGNC:610]"}, {"versioned_ensembl_gene_id":"ENSG00000256725.1","gene_symbol":"AC095350.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130628316,"end":130716281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226605.1","gene_symbol":"AC092567.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62826064,"end":62858438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224583.1","gene_symbol":"AL356277.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74642384,"end":74652002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248449.2","gene_symbol":"PCDHGB8P","gene_name":"protocadherin gamma subfamily B, 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8715]","synonyms":"PCDH-PSI3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"56120","summary":null,"start":141426286,"end":141429158,"strand":1,"description":"protocadherin gamma subfamily B, 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8715]"}, {"versioned_ensembl_gene_id":"ENSG00000259964.6","gene_symbol":"THSD4-AS1","gene_name":"THSD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51420]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929196","summary":null,"start":71147650,"end":71189042,"strand":-1,"description":"THSD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51420]"}, {"versioned_ensembl_gene_id":"ENSG00000177369.8","gene_symbol":"FLJ40194","gene_name":"uncharacterized FLJ40194 [Source:NCBI gene;Acc:124871]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"124871","summary":null,"start":49248239,"end":49258662,"strand":1,"description":"uncharacterized FLJ40194 [Source:NCBI gene;Acc:124871]"}, {"versioned_ensembl_gene_id":"ENSG00000132591.11","gene_symbol":"ERAL1","gene_name":"Era like 12S mitochondrial rRNA chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3424]","synonyms":"HERA-B","biotype":"protein_coding","ncbi_id":"26284","summary":"The protein encoded by this gene is a GTPase that localizes to the mitochondrion. The encoded protein binds to the 3' terminal stem loop of 12S mitochondrial rRNA and is required for proper assembly of the 28S small mitochondrial ribosomal subunit. Deletion of this gene has been shown to cause mitochondrial dysfunction, growth retardation, and apoptosis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":28854938,"end":28861067,"strand":1,"description":"Era like 12S mitochondrial rRNA chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3424]"}, {"versioned_ensembl_gene_id":"ENSG00000243063.1","gene_symbol":"IGKV3-7","gene_name":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28915","summary":null,"start":88978468,"end":88979081,"strand":-1,"description":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]"}, {"versioned_ensembl_gene_id":"ENSG00000240350.2","gene_symbol":"AC017002.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111491273,"end":111570974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269288.1","gene_symbol":"AC092070.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53240675,"end":53241913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229118.1","gene_symbol":"AC068491.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111265283,"end":111279880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181616.9","gene_symbol":"OR52H1","gene_name":"olfactory receptor family 52 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390067","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5544489,"end":5548533,"strand":-1,"description":"olfactory receptor family 52 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:15218]"}, {"versioned_ensembl_gene_id":"ENSG00000177283.7","gene_symbol":"FZD8","gene_name":"frizzled class receptor 8 [Source:HGNC Symbol;Acc:HGNC:4046]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8325","summary":"This intronless gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This gene is highly expressed in two human cancer cell lines, indicating that it may play a role in several types of cancer. The crystal structure of the extracellular cysteine-rich domain of a similar mouse protein has been determined. [provided by RefSeq, Jul 2008]","start":35638249,"end":35642278,"strand":-1,"description":"frizzled class receptor 8 [Source:HGNC Symbol;Acc:HGNC:4046]"}, {"versioned_ensembl_gene_id":"ENSG00000183723.12","gene_symbol":"CMTM4","gene_name":"CKLF like MARVEL transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19175]","synonyms":"CKLFSF4","biotype":"protein_coding","ncbi_id":"146223","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":66614750,"end":66696707,"strand":-1,"description":"CKLF like MARVEL transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19175]"}, {"versioned_ensembl_gene_id":"ENSG00000198398.2","gene_symbol":"TMEM207","gene_name":"transmembrane protein 207 [Source:HGNC Symbol;Acc:HGNC:33705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"131920","summary":null,"start":190428655,"end":190449876,"strand":-1,"description":"transmembrane protein 207 [Source:HGNC Symbol;Acc:HGNC:33705]"}, {"versioned_ensembl_gene_id":"ENSG00000248553.1","gene_symbol":"OR52H2P","gene_name":"olfactory receptor family 52 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15219]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"81261","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5551662,"end":5552563,"strand":-1,"description":"olfactory receptor family 52 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15219]"}, {"versioned_ensembl_gene_id":"ENSG00000269001.2","gene_symbol":"AC092070.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53197111,"end":53214522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161558.10","gene_symbol":"TMEM143","gene_name":"transmembrane protein 143 [Source:HGNC Symbol;Acc:HGNC:25603]","synonyms":"FLJ10922","biotype":"protein_coding","ncbi_id":"55260","summary":null,"start":48332356,"end":48364237,"strand":-1,"description":"transmembrane protein 143 [Source:HGNC Symbol;Acc:HGNC:25603]"}, {"versioned_ensembl_gene_id":"ENSG00000160182.2","gene_symbol":"TFF1","gene_name":"trefoil factor 1 [Source:HGNC Symbol;Acc:HGNC:11755]","synonyms":"pS2,pNR-2,HPS2,HP1.A,D21S21,BCEI","biotype":"protein_coding","ncbi_id":"7031","summary":"Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer, and affect healing of the epithelium. This gene, which is expressed in the gastric mucosa, has also been studied because of its expression in human tumors. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21. [provided by RefSeq, Jul 2008]","start":42362282,"end":42366594,"strand":-1,"description":"trefoil factor 1 [Source:HGNC Symbol;Acc:HGNC:11755]"}, {"versioned_ensembl_gene_id":"ENSG00000205038.11","gene_symbol":"PKHD1L1","gene_name":"PKHD1 like 1 [Source:HGNC Symbol;Acc:HGNC:20313]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93035","summary":null,"start":109362477,"end":109530330,"strand":1,"description":"PKHD1 like 1 [Source:HGNC Symbol;Acc:HGNC:20313]"}, {"versioned_ensembl_gene_id":"ENSG00000187483.9","gene_symbol":"SERPINA13P","gene_name":"serpin family A member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:30909]","synonyms":"UNQ6121,SERPINA13","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388007","summary":null,"start":94640725,"end":94646994,"strand":1,"description":"serpin family A member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:30909]"}, {"versioned_ensembl_gene_id":"ENSG00000258805.1","gene_symbol":"ADIPOR1P2","gene_name":"adiponectin receptor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44911]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390503","summary":null,"start":94633705,"end":94634524,"strand":1,"description":"adiponectin receptor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44911]"}, {"versioned_ensembl_gene_id":"ENSG00000248569.1","gene_symbol":"AC026410.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80351021,"end":80351956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227087.4","gene_symbol":"RBMX2P5","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391804","summary":null,"start":80331573,"end":80332541,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39927]"}, {"versioned_ensembl_gene_id":"ENSG00000283251.1","gene_symbol":"AC008687.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49056088,"end":49058761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268108.1","gene_symbol":"AC008687.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49060613,"end":49061132,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247373.3","gene_symbol":"AC055713.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123575891,"end":123585115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267091.1","gene_symbol":"CTBP2P7","gene_name":"C-terminal binding protein 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45199]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401914","summary":null,"start":36496916,"end":36498159,"strand":-1,"description":"C-terminal binding protein 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45199]"}, {"versioned_ensembl_gene_id":"ENSG00000265474.1","gene_symbol":"AC010761.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28745569,"end":28747652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265840.1","gene_symbol":"AC010761.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28749731,"end":28750079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275688.4","gene_symbol":"CCL15-CCL14","gene_name":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]","synonyms":null,"biotype":"protein_coding","ncbi_id":"348249","summary":"A cluster of CC chemokine genes exists on chromosome 17q11.2. The CC chemokines are secreted proteins characterized by two adjacent cysteines. The genes chemokine (C-C motif) ligand 14 and chemokine (C-C motif) ligand 15 are adjacent loci and express read-through transcripts spanning both loci. The read-through transcripts were originally interpreted as bicistronic transcripts, but they are represented as non-coding because they are candidates for nonsense-mediated mRNA decay (NMD). [provided by RefSeq, Dec 2009]","start":35983656,"end":36001621,"strand":-1,"description":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]"}, {"versioned_ensembl_gene_id":"ENSG00000278079.6","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816470,"end":54830813,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000230484.2","gene_symbol":"OR51A10P","gene_name":"olfactory receptor family 51 subfamily A member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:15185]","synonyms":"OR51A13,OR51A11P","biotype":"unitary_pseudogene","ncbi_id":"81295","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5468486,"end":5469422,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:15185]"}, {"versioned_ensembl_gene_id":"ENSG00000113790.10","gene_symbol":"EHHADH","gene_name":"enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3247]","synonyms":"ECHD","biotype":"protein_coding","ncbi_id":"1962","summary":"The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":185190624,"end":185281990,"strand":-1,"description":"enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3247]"}, {"versioned_ensembl_gene_id":"ENSG00000076604.14","gene_symbol":"TRAF4","gene_name":"TNF receptor associated factor 4 [Source:HGNC Symbol;Acc:HGNC:12034]","synonyms":"CART1,RNF83,MLN62","biotype":"protein_coding","ncbi_id":"9618","summary":"This gene encodes a member of the TNF receptor associated factor (TRAF) family. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. The encoded protein has been shown to interact with neurotrophin receptor, p75 (NTR/NTSR1), and negatively regulate NTR induced cell death and NF-kappa B activation. This protein has been found to bind to p47phox, a cytosolic regulatory factor included in a multi-protein complex known as NAD(P)H oxidase. This protein thus, is thought to be involved in the oxidative activation of MAPK8/JNK. Alternatively spliced transcript variants have been observed but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]","start":28743984,"end":28750958,"strand":1,"description":"TNF receptor associated factor 4 [Source:HGNC Symbol;Acc:HGNC:12034]"}, {"versioned_ensembl_gene_id":"ENSG00000109787.12","gene_symbol":"KLF3","gene_name":"Kruppel like factor 3 [Source:HGNC Symbol;Acc:HGNC:16516]","synonyms":"BKLF","biotype":"protein_coding","ncbi_id":"51274","summary":null,"start":38664196,"end":38701042,"strand":1,"description":"Kruppel like factor 3 [Source:HGNC Symbol;Acc:HGNC:16516]"}, {"versioned_ensembl_gene_id":"ENSG00000144451.18","gene_symbol":"SPAG16","gene_name":"sperm associated antigen 16 [Source:HGNC Symbol;Acc:HGNC:23225]","synonyms":"WDR29,PF20,FLJ22724,DKFZp666P1710","biotype":"protein_coding","ncbi_id":"79582","summary":"Cilia and flagella are comprised of a microtubular backbone, the axoneme, which is organized by the basal body and surrounded by plasma membrane. SPAG16 encodes 2 major proteins that associate with the axoneme of sperm tail and the nucleus of postmeiotic germ cells, respectively (Zhang et al., 2007 [PubMed 17699735]).[supplied by OMIM, Jul 2008]","start":213284379,"end":214410501,"strand":1,"description":"sperm associated antigen 16 [Source:HGNC Symbol;Acc:HGNC:23225]"}, {"versioned_ensembl_gene_id":"ENSG00000213917.2","gene_symbol":"RPL5P8","gene_name":"ribosomal protein L5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130523","summary":null,"start":214280638,"end":214281452,"strand":-1,"description":"ribosomal protein L5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36290]"}, {"versioned_ensembl_gene_id":"ENSG00000187068.2","gene_symbol":"C3orf70","gene_name":"chromosome 3 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33731]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285382","summary":null,"start":185078050,"end":185153014,"strand":-1,"description":"chromosome 3 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33731]"}, {"versioned_ensembl_gene_id":"ENSG00000232849.1","gene_symbol":"LINC00363","gene_name":"long intergenic non-protein coding RNA 363 [Source:HGNC Symbol;Acc:HGNC:42684]","synonyms":"TCONS_00021586","biotype":"lincRNA","ncbi_id":"104326053","summary":null,"start":93056657,"end":93057926,"strand":1,"description":"long intergenic non-protein coding RNA 363 [Source:HGNC Symbol;Acc:HGNC:42684]"}, {"versioned_ensembl_gene_id":"ENSG00000267099.1","gene_symbol":"NTF6G","gene_name":"neurotrophin 6 gamma (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8027]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"4912","summary":null,"start":49029726,"end":49030341,"strand":1,"description":"neurotrophin 6 gamma (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8027]"}, {"versioned_ensembl_gene_id":"ENSG00000168214.20","gene_symbol":"RBPJ","gene_name":"recombination signal binding protein for immunoglobulin kappa J region [Source:HGNC Symbol;Acc:HGNC:5724]","synonyms":"SUH,RBPSUH,RBPJK,RBP-J,KBF2,IGKJRB1,IGKJRB,CBF1","biotype":"protein_coding","ncbi_id":"3516","summary":"The protein encoded by this gene is a transcriptional regulator important in the Notch signaling pathway. The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins. It is thought to function by recruiting chromatin remodeling complexes containing histone deacetylase or histone acetylase proteins to Notch signaling pathway genes. Several transcript variants encoding different isoforms have been found for this gene, and several pseudogenes of this gene exist on chromosome 9. [provided by RefSeq, Oct 2013]","start":26163455,"end":26435131,"strand":1,"description":"recombination signal binding protein for immunoglobulin kappa J region [Source:HGNC Symbol;Acc:HGNC:5724]"}, {"versioned_ensembl_gene_id":"ENSG00000186017.14","gene_symbol":"ZNF566","gene_name":"zinc finger protein 566 [Source:HGNC Symbol;Acc:HGNC:25919]","synonyms":"MGC12515,FLJ14779","biotype":"protein_coding","ncbi_id":"84924","summary":null,"start":36445119,"end":36489902,"strand":-1,"description":"zinc finger protein 566 [Source:HGNC Symbol;Acc:HGNC:25919]"}, {"versioned_ensembl_gene_id":"ENSG00000233607.1","gene_symbol":"LINC01392","gene_name":"long intergenic non-protein coding RNA 1392 [Source:HGNC Symbol;Acc:HGNC:50668]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355291","summary":null,"start":115061537,"end":115231355,"strand":-1,"description":"long intergenic non-protein coding RNA 1392 [Source:HGNC Symbol;Acc:HGNC:50668]"}, {"versioned_ensembl_gene_id":"ENSG00000277748.1","gene_symbol":"AC006262.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46249394,"end":46250163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184293.7","gene_symbol":"CLECL1","gene_name":"C-type lectin like 1 [Source:HGNC Symbol;Acc:HGNC:24462]","synonyms":"DCAL1","biotype":"protein_coding","ncbi_id":"160365","summary":"This gene encodes a type II transmembrane, C-type lectin-like protein that is highly expressed on dendritic and B cells. This protein may act as a T-cell costimulatory molecule that enhances interleukin-4 production, and maybe involved in the regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":9715860,"end":9733299,"strand":-1,"description":"C-type lectin like 1 [Source:HGNC Symbol;Acc:HGNC:24462]"}, {"versioned_ensembl_gene_id":"ENSG00000232174.3","gene_symbol":"AC113340.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138620329,"end":138620964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105393.15","gene_symbol":"BABAM1","gene_name":"BRISC and BRCA1 A complex member 1 [Source:HGNC Symbol;Acc:HGNC:25008]","synonyms":"NBA1,MERIT40,HSPC142,FLJ20571,C19orf62","biotype":"protein_coding","ncbi_id":"29086","summary":null,"start":17267350,"end":17281249,"strand":1,"description":"BRISC and BRCA1 A complex member 1 [Source:HGNC Symbol;Acc:HGNC:25008]"}, {"versioned_ensembl_gene_id":"ENSG00000124172.9","gene_symbol":"ATP5E","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit [Source:HGNC Symbol;Acc:HGNC:838]","synonyms":null,"biotype":"protein_coding","ncbi_id":"514","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the epsilon subunit of the catalytic core. Two pseudogenes of this gene are located on chromosomes 4 and 13. Read-through transcripts that include exons from this gene are expressed from the upstream gene SLMO2.[provided by RefSeq, Mar 2011]","start":59025467,"end":59032382,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit [Source:HGNC Symbol;Acc:HGNC:838]"}, {"versioned_ensembl_gene_id":"ENSG00000005812.10","gene_symbol":"FBXL3","gene_name":"F-box and leucine rich repeat protein 3 [Source:HGNC Symbol;Acc:HGNC:13599]","synonyms":"FBXL3A,FBL3A,FBL3","biotype":"protein_coding","ncbi_id":"26224","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats and is localized in the nucleus. [provided by RefSeq, Jul 2008]","start":76992598,"end":77027195,"strand":-1,"description":"F-box and leucine rich repeat protein 3 [Source:HGNC Symbol;Acc:HGNC:13599]"}, {"versioned_ensembl_gene_id":"ENSG00000095906.16","gene_symbol":"NUBP2","gene_name":"nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8042]","synonyms":"CFD1","biotype":"protein_coding","ncbi_id":"10101","summary":"This gene encodes an adenosine triphosphate (ATP) and metal-binding protein that is required for the assembly of cyotosolic iron-sulfur proteins. The encoded protein functions in a heterotetramer with nucleotide-binding protein 1 (NUBP1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2013]","start":1782901,"end":1789191,"strand":1,"description":"nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8042]"}, {"versioned_ensembl_gene_id":"ENSG00000165650.11","gene_symbol":"PDZD8","gene_name":"PDZ domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26974]","synonyms":"PDZK8,FLJ34427,bA129M16.2","biotype":"protein_coding","ncbi_id":"118987","summary":null,"start":117277274,"end":117375467,"strand":-1,"description":"PDZ domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26974]"}, {"versioned_ensembl_gene_id":"ENSG00000065371.17","gene_symbol":"ROPN1","gene_name":"rhophilin associated tail protein 1 [Source:HGNC Symbol;Acc:HGNC:17692]","synonyms":"ropporin,ROPN1A,ODF6,CT91","biotype":"protein_coding","ncbi_id":"54763","summary":"The protein encoded by this gene is found in the fibrous sheath of spermatazoa, where it interacts with rhophilin, a Rho GTPase binding protein. The encoded protein also can bind an A-kinase anchoring protein (AKAP110) and a calcium-binding tyrosine phosphorylation-regulated protein (CABYR). This protein may be involved in sperm motility and has been shown to be a cancer-testis antigen in hematologic malignancies. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":123968521,"end":123992178,"strand":-1,"description":"rhophilin associated tail protein 1 [Source:HGNC Symbol;Acc:HGNC:17692]"}, {"versioned_ensembl_gene_id":"ENSG00000264595.1","gene_symbol":"AC103808.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76227990,"end":76233387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229988.1","gene_symbol":"HBBP1","gene_name":"hemoglobin subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4828]","synonyms":"HBHP,HBH1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3044","summary":null,"start":5241954,"end":5243537,"strand":-1,"description":"hemoglobin subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4828]"}, {"versioned_ensembl_gene_id":"ENSG00000268964.1","gene_symbol":"ERVV-2","gene_name":"endogenous retrovirus group V member 2, envelope [Source:HGNC Symbol;Acc:HGNC:39051]","synonyms":"ENVV2","biotype":"protein_coding","ncbi_id":"100271846","summary":"Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on human chromosome 19 that has inactivating mutations in the gag and pol genes. This envelope glycoprotein gene appears to have been selectively preserved. The gene's protein product is expressed in the placenta and acts as a syncytin in Old World monkeys, but has lost the fusogenic activity in humans and other primate lineages. [provided by RefSeq, Jun 2015]","start":53044738,"end":53051076,"strand":1,"description":"endogenous retrovirus group V member 2, envelope [Source:HGNC Symbol;Acc:HGNC:39051]"}, {"versioned_ensembl_gene_id":"ENSG00000264444.1","gene_symbol":"AC096708.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68866517,"end":68867028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267757.4","gene_symbol":"EML2-AS1","gene_name":"EML2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48331]","synonyms":"C19orf83","biotype":"processed_transcript","ncbi_id":"100287177","summary":null,"start":45641494,"end":45642840,"strand":1,"description":"EML2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48331]"}, {"versioned_ensembl_gene_id":"ENSG00000273485.1","gene_symbol":"AL139339.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103450196,"end":103450852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269480.1","gene_symbol":"AC020913.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17207138,"end":17208010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226115.1","gene_symbol":"AP001476.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46056516,"end":46057567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242866.9","gene_symbol":"STRC","gene_name":"stereocilin [Source:HGNC Symbol;Acc:HGNC:16035]","synonyms":"DFNB16","biotype":"protein_coding","ncbi_id":"161497","summary":"This gene encodes a protein that is associated with the hair bundle of the sensory hair cells in the inner ear. The hair bundle is composed of stiff microvilli called stereocilia and is involved with mechanoreception of sound waves. This gene is part of a tandem duplication on chromosome 15; the second copy is a pseudogene. Mutations in this gene cause autosomal recessive non-syndromic deafness. [provided by RefSeq, Jul 2008]","start":43599398,"end":43618800,"strand":-1,"description":"stereocilin [Source:HGNC Symbol;Acc:HGNC:16035]"}, {"versioned_ensembl_gene_id":"ENSG00000125788.5","gene_symbol":"DEFB126","gene_name":"defensin beta 126 [Source:HGNC Symbol;Acc:HGNC:15900]","synonyms":"DEFB-26,C20orf8,bA530N10.1","biotype":"protein_coding","ncbi_id":"81623","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. The encoded protein is highly similar to an epididymal-specific secretory protein (ESP13.2) from cynomolgus monkey. Mutation of this gene is associated with impaired sperm function. [provided by RefSeq, Nov 2014]","start":142369,"end":145751,"strand":1,"description":"defensin beta 126 [Source:HGNC Symbol;Acc:HGNC:15900]"}, {"versioned_ensembl_gene_id":"ENSG00000253326.2","gene_symbol":"AL606534.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":243054861,"end":243056394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215800.2","gene_symbol":"RSL24D1P4","gene_name":"ribosomal L24 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37884]","synonyms":"RSL24D1P19","biotype":"processed_pseudogene","ncbi_id":"391183","summary":null,"start":242772620,"end":242773103,"strand":1,"description":"ribosomal L24 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37884]"}, {"versioned_ensembl_gene_id":"ENSG00000234484.1","gene_symbol":"AL032821.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132752675,"end":132753951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227000.2","gene_symbol":"HSPD1P14","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35143]","synonyms":"HSPD1-17P","biotype":"processed_pseudogene","ncbi_id":"100287140","summary":null,"start":33838523,"end":33840140,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35143]"}, {"versioned_ensembl_gene_id":"ENSG00000258584.1","gene_symbol":"FAM181A-AS1","gene_name":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]","synonyms":"C14orf86","biotype":"antisense_RNA","ncbi_id":"283592","summary":null,"start":93904730,"end":93927066,"strand":-1,"description":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]"}, {"versioned_ensembl_gene_id":"ENSG00000259792.1","gene_symbol":"AC104758.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77993405,"end":77995289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231859.1","gene_symbol":"AC079781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97906429,"end":97906822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258872.2","gene_symbol":"FDPSP3","gene_name":"farnesyl diphosphate synthase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3634]","synonyms":"FPSL3,FDPSL3","biotype":"transcribed_processed_pseudogene","ncbi_id":"2227","summary":null,"start":54884849,"end":54886213,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3634]"}, {"versioned_ensembl_gene_id":"ENSG00000231543.9","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31879966,"end":31927861,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000267405.1","gene_symbol":"AC005180.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44794747,"end":44797783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177234.7","gene_symbol":"LINC01561","gene_name":"long intergenic non-protein coding RNA 1561 [Source:HGNC Symbol;Acc:HGNC:31365]","synonyms":"FLJ37402,Em:AC023282.2,C10orf85","biotype":"lincRNA","ncbi_id":"404216","summary":null,"start":120597949,"end":120600124,"strand":1,"description":"long intergenic non-protein coding RNA 1561 [Source:HGNC Symbol;Acc:HGNC:31365]"}, {"versioned_ensembl_gene_id":"ENSG00000267505.1","gene_symbol":"AC005180.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44793199,"end":44794474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100351.16","gene_symbol":"GRAP2","gene_name":"GRB2-related adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:4563]","synonyms":"Mona,Grf40,GrbX,GRBLG,GADS","biotype":"protein_coding","ncbi_id":"9402","summary":"This gene encodes a member of the GRB2/Sem5/Drk family. This member is an adaptor-like protein involved in leukocyte-specific protein-tyrosine kinase signaling. Like its related family member, GRB2-related adaptor protein (GRAP), this protein contains an SH2 domain flanked by two SH3 domains. This protein interacts with other proteins, such as GRB2-associated binding protein 1 (GAB1) and the SLP-76 leukocyte protein (LCP2), through its SH3 domains. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":39901082,"end":39973721,"strand":1,"description":"GRB2-related adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:4563]"}, {"versioned_ensembl_gene_id":"ENSG00000049883.14","gene_symbol":"PTCD2","gene_name":"pentatricopeptide repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:25734]","synonyms":"FLJ12598","biotype":"protein_coding","ncbi_id":"79810","summary":null,"start":72320367,"end":72368395,"strand":1,"description":"pentatricopeptide repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:25734]"}, {"versioned_ensembl_gene_id":"ENSG00000268734.1","gene_symbol":"AC245128.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54890673,"end":54891420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226533.1","gene_symbol":"BTBD9-AS1","gene_name":"BTBD9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40959]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929425","summary":null,"start":38481692,"end":38482531,"strand":1,"description":"BTBD9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40959]"}, {"versioned_ensembl_gene_id":"ENSG00000171451.13","gene_symbol":"DSEL","gene_name":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]","synonyms":"FLJ11477,DE-epi2,C18orf4,NCAG1","biotype":"protein_coding","ncbi_id":"92126","summary":null,"start":67506582,"end":67516980,"strand":-1,"description":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]"}, {"versioned_ensembl_gene_id":"ENSG00000265533.1","gene_symbol":"AC114689.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67516546,"end":67899619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224446.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529354,"end":29533502,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000230791.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31576870,"end":31579655,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000173966.7","gene_symbol":"AC095040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53575713,"end":53576387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177051.5","gene_symbol":"FBXO46","gene_name":"F-box protein 46 [Source:HGNC Symbol;Acc:HGNC:25069]","synonyms":"FBXO34L,Fbx46,20D7-FC4","biotype":"protein_coding","ncbi_id":"23403","summary":"Members of the F-box protein family, such as FBXO46, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":45710629,"end":45730904,"strand":-1,"description":"F-box protein 46 [Source:HGNC Symbol;Acc:HGNC:25069]"}, {"versioned_ensembl_gene_id":"ENSG00000266707.1","gene_symbol":"AC006120.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66197693,"end":66198238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164400.5","gene_symbol":"CSF2","gene_name":"colony stimulating factor 2 [Source:HGNC Symbol;Acc:HGNC:2434]","synonyms":"GMCSF,GM-CSF","biotype":"protein_coding","ncbi_id":"1437","summary":"The protein encoded by this gene is a cytokine that controls the production, differentiation, and function of granulocytes and macrophages. The active form of the protein is found extracellularly as a homodimer. This gene has been localized to a cluster of related genes at chromosome region 5q31, which is known to be associated with interstitial deletions in the 5q- syndrome and acute myelogenous leukemia. Other genes in the cluster include those encoding interleukins 4, 5, and 13. This gene plays a role in promoting tissue inflammation. Elevated levels of cytokines, including the one produced by this gene, have been detected in SARS-CoV-2 infected patients that develop acute respiratory distress syndrome. Mice deficient in this gene or its receptor develop pulmonary alveolar proteinosis. [provided by RefSeq, Aug 2020]","start":132073790,"end":132076170,"strand":1,"description":"colony stimulating factor 2 [Source:HGNC Symbol;Acc:HGNC:2434]"}, {"versioned_ensembl_gene_id":"ENSG00000224475.1","gene_symbol":"AC073900.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97200708,"end":97201483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135144.7","gene_symbol":"DTX1","gene_name":"deltex E3 ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:3060]","synonyms":"hDx-1","biotype":"protein_coding","ncbi_id":"1840","summary":"Studies in Drosophila have identified this gene as encoding a positive regulator of the Notch-signaling pathway. The human gene encodes a protein of unknown function; however, it may play a role in basic helix-loop-helix transcription factor activity. [provided by RefSeq, Jul 2008]","start":113056709,"end":113098028,"strand":1,"description":"deltex E3 ubiquitin ligase 1 [Source:HGNC Symbol;Acc:HGNC:3060]"}, {"versioned_ensembl_gene_id":"ENSG00000265142.8","gene_symbol":"MIR133A1HG","gene_name":"MIR133A1 host gene [Source:HGNC Symbol;Acc:HGNC:49594]","synonyms":"MIR1-2HG","biotype":"antisense_RNA","ncbi_id":"102723167","summary":null,"start":21825487,"end":21831410,"strand":-1,"description":"MIR133A1 host gene [Source:HGNC Symbol;Acc:HGNC:49594]"}, {"versioned_ensembl_gene_id":"ENSG00000129244.8","gene_symbol":"ATP1B2","gene_name":"ATPase Na+/K+ transporting subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:805]","synonyms":"AMOG","biotype":"protein_coding","ncbi_id":"482","summary":"The protein encoded by this gene belongs to the family of Na+/K+ and H+/K+ ATPases beta chain proteins, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The beta subunit regulates, through assembly of alpha/beta heterodimers, the number of sodium pumps transported to the plasma membrane. The glycoprotein subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes a beta 2 subunit. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":7646627,"end":7657768,"strand":1,"description":"ATPase Na+/K+ transporting subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:805]"}, {"versioned_ensembl_gene_id":"ENSG00000280019.1","gene_symbol":"CU633906.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6272135,"end":6276532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275552.1","gene_symbol":"AC243965.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22595808,"end":22598946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159658.10","gene_symbol":"EFCAB14","gene_name":"EF-hand calcium binding domain 14 [Source:HGNC Symbol;Acc:HGNC:29051]","synonyms":"KIAA0494","biotype":"protein_coding","ncbi_id":"9813","summary":null,"start":46675159,"end":46719064,"strand":-1,"description":"EF-hand calcium binding domain 14 [Source:HGNC Symbol;Acc:HGNC:29051]"}, {"versioned_ensembl_gene_id":"ENSG00000277171.1","gene_symbol":"AC010975.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":79547151,"end":79548128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162951.10","gene_symbol":"LRRTM1","gene_name":"leucine rich repeat transmembrane neuronal 1 [Source:HGNC Symbol;Acc:HGNC:19408]","synonyms":"FLJ32082","biotype":"protein_coding","ncbi_id":"347730","summary":null,"start":80288351,"end":80304749,"strand":-1,"description":"leucine rich repeat transmembrane neuronal 1 [Source:HGNC Symbol;Acc:HGNC:19408]"}, {"versioned_ensembl_gene_id":"ENSG00000242473.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755023,"end":54767371,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000221957.8","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832676,"end":54848569,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000281354.1","gene_symbol":"AP000350.13","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23856427,"end":23857039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166049.10","gene_symbol":"PASD1","gene_name":"PAS domain containing repressor 1 [Source:HGNC Symbol;Acc:HGNC:20686]","synonyms":"CT63","biotype":"protein_coding","ncbi_id":"139135","summary":"This gene encodes a protein that is thought to function as a transcription factor. The protein is a cancer-associated antigen that can stimulate autologous T-cell responses, and it is therefore considered to be a potential immunotherapeutic target for the treatment of various hematopoietic malignancies, including diffuse large B-cell lymphoma. [provided by RefSeq, May 2010]","start":151563622,"end":151676739,"strand":1,"description":"PAS domain containing repressor 1 [Source:HGNC Symbol;Acc:HGNC:20686]"}, {"versioned_ensembl_gene_id":"ENSG00000284658.1","gene_symbol":"AL513478.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66204896,"end":66208833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092841.18","gene_symbol":"MYL6","gene_name":"myosin light chain 6 [Source:HGNC Symbol;Acc:HGNC:7587]","synonyms":"MLC3NM,MLC1SM,ESMLC","biotype":"protein_coding","ncbi_id":"4637","summary":"Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain that is expressed in smooth muscle and non-muscle tissues. Genomic sequences representing several pseudogenes have been described and two transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":56158161,"end":56163496,"strand":1,"description":"myosin light chain 6 [Source:HGNC Symbol;Acc:HGNC:7587]"}, {"versioned_ensembl_gene_id":"ENSG00000284611.1","gene_symbol":"AL513478.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66182326,"end":66188451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259828.1","gene_symbol":"AL355596.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141447011,"end":141451006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179476.7","gene_symbol":"C14orf28","gene_name":"chromosome 14 open reading frame 28 [Source:HGNC Symbol;Acc:HGNC:19834]","synonyms":"DRIP-1","biotype":"protein_coding","ncbi_id":"122525","summary":null,"start":44897295,"end":44907257,"strand":1,"description":"chromosome 14 open reading frame 28 [Source:HGNC Symbol;Acc:HGNC:19834]"}, {"versioned_ensembl_gene_id":"ENSG00000234147.1","gene_symbol":"AL035446.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140845958,"end":140852924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148204.11","gene_symbol":"CRB2","gene_name":"crumbs 2, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:18688]","synonyms":"FLJ38464,FLJ16786","biotype":"protein_coding","ncbi_id":"286204","summary":"This gene encodes a member of a family of proteins that are components of the Crumbs cell polarity complex. In mammals, members of this family are thought to play a role in many cellular processes in early embryonic development. A similar protein in Drosophila determines apicobasal polarity in embryonic epithelial cells. Mutations in this gene are associated with focal segmental glomerulosclerosis 9, and with ventriculomegaly with cystic kidney disease. [provided by RefSeq, Aug 2016]","start":123356170,"end":123380324,"strand":1,"description":"crumbs 2, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:18688]"}, {"versioned_ensembl_gene_id":"ENSG00000214176.9","gene_symbol":"PLEKHM1P1","gene_name":"pleckstrin homology and RUN domain containing M1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35411]","synonyms":"PLEKHM1P,LOC440456","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440456","summary":null,"start":64779259,"end":64837154,"strand":-1,"description":"pleckstrin homology and RUN domain containing M1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35411]"}, {"versioned_ensembl_gene_id":"ENSG00000170786.12","gene_symbol":"SDR16C5","gene_name":"short chain dehydrogenase/reductase family 16C member 5 [Source:HGNC Symbol;Acc:HGNC:30311]","synonyms":"RDHE2,RDH-E2,EPHD-2","biotype":"protein_coding","ncbi_id":"195814","summary":"This gene encodes a member of the short-chain alcohol dehydrogenase/reductase superfamily of proteins and is involved in the oxidation of retinol to retinaldehyde. The encoded protein is associated with the endoplasmic reticulum and is predicted to contain three transmembrane helices, suggesting that it is an integral membrane protein. It recognizes all-trans-retinol and all-trans-retinaldehyde as substrates and exhibits a strong preference for NAD(+)/NADH as cofactors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":56300010,"end":56320776,"strand":-1,"description":"short chain dehydrogenase/reductase family 16C member 5 [Source:HGNC Symbol;Acc:HGNC:30311]"}, {"versioned_ensembl_gene_id":"ENSG00000119522.16","gene_symbol":"DENND1A","gene_name":"DENN domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29324]","synonyms":"KIAA1608,FLJ21129,FAM31A","biotype":"protein_coding","ncbi_id":"57706","summary":"Clathrin (see MIM 118955)-mediated endocytosis is a major mechanism for internalization of proteins and lipids. Members of the connecdenn family, such as DENND1A, function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2; see MIM 601024). Thus, connecdenns link RAB35 activation with the clathrin machinery (Marat and McPherson, 2010 [PubMed 20154091]).[supplied by OMIM, Nov 2010]","start":123379654,"end":123930152,"strand":-1,"description":"DENN domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29324]"}, {"versioned_ensembl_gene_id":"ENSG00000171159.4","gene_symbol":"C9orf16","gene_name":"chromosome 9 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:17823]","synonyms":"MGC4639,FLJ12823,EST00098","biotype":"protein_coding","ncbi_id":"79095","summary":null,"start":128160260,"end":128163928,"strand":1,"description":"chromosome 9 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:17823]"}, {"versioned_ensembl_gene_id":"ENSG00000211875.1","gene_symbol":"TRAJ14","gene_name":"T-cell receptor alpha joining 14 [Source:HGNC Symbol;Acc:HGNC:12042]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28741","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22530327,"end":22530378,"strand":1,"description":"T-cell receptor alpha joining 14 [Source:HGNC Symbol;Acc:HGNC:12042]"}, {"versioned_ensembl_gene_id":"ENSG00000174684.6","gene_symbol":"B4GAT1","gene_name":"beta-1,4-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15685]","synonyms":"iGNT,iGAT,BETA3GNTI,B3GNT6,B3GNT1,B3GN-T1","biotype":"protein_coding","ncbi_id":"11041","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II transmembrane protein. It is essential for the synthesis of poly-N-acetyllactosamine, a determinant for the blood group i antigen. [provided by RefSeq, Jul 2008]","start":66345372,"end":66347692,"strand":-1,"description":"beta-1,4-glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15685]"}, {"versioned_ensembl_gene_id":"ENSG00000258633.1","gene_symbol":"AL049870.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44876874,"end":44897077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198719.8","gene_symbol":"DLL1","gene_name":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28514","summary":" DLL1 is a human homolog of the Notch Delta ligand and is a member of the delta/serrate/jagged family. It plays a role in mediating cell fate decisions during hematopoiesis. It may play a role in cell-to-cell communication. [provided by RefSeq, Jul 2008]","start":170282206,"end":170306565,"strand":-1,"description":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]"}, {"versioned_ensembl_gene_id":"ENSG00000196696.12","gene_symbol":"PDXDC2P-NPIPB14P","gene_name":"nuclear pore complex-interacting protein [Source:NCBI gene;Acc:283970]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283970","summary":"This locus represents naturally-occurring readthrough transcription between two pseudogenes, PDXDC2P (pyridoxal dependent decarboxylase domain containing 2, pseudogene) and NPIPB14P (nuclear pore complex interacting protein family, member B14, pseudogene). The individual pseudogene loci are not curated as transcribed regions. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Feb 2017]","start":69976297,"end":70065948,"strand":-1,"description":"nuclear pore complex-interacting protein [Source:NCBI gene;Acc:283970]"}, {"versioned_ensembl_gene_id":"ENSG00000226232.8","gene_symbol":"NPIPB14P","gene_name":"nuclear pore complex interacting protein family member B14, pseudogene [Source:HGNC Symbol;Acc:HGNC:41990]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"109729168","summary":null,"start":69976388,"end":69996188,"strand":-1,"description":"nuclear pore complex interacting protein family member B14, pseudogene [Source:HGNC Symbol;Acc:HGNC:41990]"}, {"versioned_ensembl_gene_id":"ENSG00000228208.6","gene_symbol":"C1orf143","gene_name":"chromosome 1 open reading frame 143 [Source:HGNC Symbol;Acc:HGNC:32045]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440714","summary":null,"start":218510096,"end":218525978,"strand":1,"description":"chromosome 1 open reading frame 143 [Source:HGNC Symbol;Acc:HGNC:32045]"}, {"versioned_ensembl_gene_id":"ENSG00000167397.14","gene_symbol":"VKORC1","gene_name":"vitamin K epoxide reductase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23663]","synonyms":"VKCFD2","biotype":"protein_coding","ncbi_id":"79001","summary":"This gene encodes the catalytic subunit of the vitamin K epoxide reductase complex, which is responsible for the reduction of inactive vitamin K 2,3-epoxide to active vitamin K in the endoplasmic reticulum membrane. Vitamin K is a required co-factor for carboxylation of glutamic acid residues by vitamin K-dependent gamma-carboxylase in blood-clotting enzymes. Allelic variation in this gene is associated with vitamin k-dependent clotting factors combined deficiency of 2, and increased resistance or sensitivity to warfarin, an inhibitor of vitamin K epoxide reductase. Pseudogenes of this gene are located on chromosomes 1 and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":31090842,"end":31095980,"strand":-1,"description":"vitamin K epoxide reductase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23663]"}, {"versioned_ensembl_gene_id":"ENSG00000082153.17","gene_symbol":"BZW1","gene_name":"basic leucine zipper and W2 domains 1 [Source:HGNC Symbol;Acc:HGNC:18380]","synonyms":"KIAA0005,BZAP45","biotype":"protein_coding","ncbi_id":"9689","summary":null,"start":200810594,"end":200827338,"strand":1,"description":"basic leucine zipper and W2 domains 1 [Source:HGNC Symbol;Acc:HGNC:18380]"}, {"versioned_ensembl_gene_id":"ENSG00000176473.13","gene_symbol":"WDR25","gene_name":"WD repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:21064]","synonyms":"MGC4645,C14orf67","biotype":"protein_coding","ncbi_id":"79446","summary":"This gene encodes a protein containing 7 WD repeats. WD repeats are approximately 30 to 40-amino acid domains containing several conserved residues, typically having a Tryptophan-Aspartic acid dipeptide (WD) at the C-terminal end. WD domains are involved in protein-protein interactions in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":100376418,"end":100530303,"strand":1,"description":"WD repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:21064]"}, {"versioned_ensembl_gene_id":"ENSG00000264131.1","gene_symbol":"AC007631.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65186159,"end":65187018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145216.15","gene_symbol":"FIP1L1","gene_name":"factor interacting with PAPOLA and CPSF1 [Source:HGNC Symbol;Acc:HGNC:19124]","synonyms":"FIP1,DKFZp586K0717","biotype":"protein_coding","ncbi_id":"81608","summary":"This gene encodes a subunit of the CPSF (cleavage and polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), binds to U-rich sequences of pre-mRNA and stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-binding site and its C-terminus an RNA-binding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 and PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion and chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhibitors. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":53377643,"end":53460861,"strand":1,"description":"factor interacting with PAPOLA and CPSF1 [Source:HGNC Symbol;Acc:HGNC:19124]"}, {"versioned_ensembl_gene_id":"ENSG00000274364.1","gene_symbol":"AL110115.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31535263,"end":31535626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230613.1","gene_symbol":"HM13-AS1","gene_name":"HM13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41940]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874042","summary":null,"start":31567707,"end":31573263,"strand":-1,"description":"HM13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41940]"}, {"versioned_ensembl_gene_id":"ENSG00000280179.1","gene_symbol":"CU639417.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6084364,"end":6091407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095794.19","gene_symbol":"CREM","gene_name":"cAMP responsive element modulator [Source:HGNC Symbol;Acc:HGNC:2352]","synonyms":"hCREM-2","biotype":"protein_coding","ncbi_id":"1390","summary":"This gene encodes a bZIP transcription factor that binds to the cAMP responsive element found in many viral and cellular promoters. It is an important component of cAMP-mediated signal transduction during the spermatogenetic cycle, as well as other complex processes. Alternative promoter and translation initiation site usage allows this gene to exert spatial and temporal specificity to cAMP responsiveness. Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene, with some of them functioning as activators and some as repressors of transcription. [provided by RefSeq, Jul 2008]","start":35126791,"end":35212958,"strand":1,"description":"cAMP responsive element modulator [Source:HGNC Symbol;Acc:HGNC:2352]"}, {"versioned_ensembl_gene_id":"ENSG00000280095.1","gene_symbol":"CU639417.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6081193,"end":6082585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259503.1","gene_symbol":"AC048383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70321576,"end":70326742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233343.1","gene_symbol":"ATP6V1G1P4","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37671]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462843","summary":null,"start":35158306,"end":35158640,"strand":1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37671]"}, {"versioned_ensembl_gene_id":"ENSG00000104907.12","gene_symbol":"TRMT1","gene_name":"tRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25980]","synonyms":"TRM1,FLJ20244","biotype":"protein_coding","ncbi_id":"55621","summary":"This gene encodes a tRNA-modifying enzyme that acts as a dimethyltransferase, modifying a single guanine residue at position 26 of the tRNA. The encoded enzyme has both mono- and dimethylase activity when exogenously expressed, and uses S-adenosyl methionine as a methyl donor. The C-terminal region of the encoded protein has both a zinc finger motif, and an arginine/proline-rich region. Mutations in this gene have been implicated in autosomal recessive intellectual disorder (ARID). Alternative splicing results in multiple transcript variants encoding different isoforms. There is a pseudogene of this gene on the X chromosome. [provided by RefSeq, May 2017]","start":13104902,"end":13117567,"strand":-1,"description":"tRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25980]"}, {"versioned_ensembl_gene_id":"ENSG00000267180.1","gene_symbol":"AC007136.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":2030853,"end":2031051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267283.1","gene_symbol":"AC005306.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1989401,"end":1990370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279248.1","gene_symbol":"AP003400.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89533645,"end":89534043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269980.1","gene_symbol":"AC068768.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123262060,"end":123262402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237187.8","gene_symbol":"NR2F1-AS1","gene_name":"NR2F1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48622]","synonyms":"FLJ42709","biotype":"antisense_RNA","ncbi_id":"441094","summary":null,"start":93409359,"end":93585648,"strand":-1,"description":"NR2F1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48622]"}, {"versioned_ensembl_gene_id":"ENSG00000232667.10","gene_symbol":"AC004862.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80312574,"end":80391474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148297.15","gene_symbol":"MED22","gene_name":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]","synonyms":"SRB6,Med24,SURF5","biotype":"protein_coding","ncbi_id":"6837","summary":"This gene encodes a protein component of the mediator complex, which functions in the regulation of transcription by bridging interactions between gene-specific regulatory factors, RNA polymerase II, and general transcription factors. Alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2013]","start":133338323,"end":133348131,"strand":-1,"description":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]"}, {"versioned_ensembl_gene_id":"ENSG00000235976.2","gene_symbol":"Z80107.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101989481,"end":101989872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267374.1","gene_symbol":"AC016205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39206924,"end":39800318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157796.17","gene_symbol":"WDR19","gene_name":"WD repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:18340]","synonyms":"Pwdmp,Oseg6,ORF26,NPHP13,KIAA1638,IFT144,FLJ23127,DYF-2","biotype":"protein_coding","ncbi_id":"57728","summary":"The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":39182404,"end":39285810,"strand":1,"description":"WD repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:18340]"}, {"versioned_ensembl_gene_id":"ENSG00000280024.1","gene_symbol":"AC048347.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127372243,"end":127372669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279952.1","gene_symbol":"AC068787.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127462507,"end":127463197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214415.3","gene_symbol":"GNAT3","gene_name":"G protein subunit alpha transducin 3 [Source:HGNC Symbol;Acc:HGNC:22800]","synonyms":"gustducin,GDCA","biotype":"protein_coding","ncbi_id":"346562","summary":"Sweet, bitter, and umami tastes are transmitted from taste receptors by a specific guanine nucleotide binding protein. The protein encoded by this gene is the alpha subunit of this heterotrimeric G protein, which is found not only in the oral epithelium but also in gut tissues. Variations in this gene have been linked to metabolic syndrome. [provided by RefSeq, Dec 2015]","start":80458671,"end":80512020,"strand":-1,"description":"G protein subunit alpha transducin 3 [Source:HGNC Symbol;Acc:HGNC:22800]"}, {"versioned_ensembl_gene_id":"ENSG00000258283.1","gene_symbol":"AC011603.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48995150,"end":48996334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175745.11","gene_symbol":"NR2F1","gene_name":"nuclear receptor subfamily 2 group F member 1 [Source:HGNC Symbol;Acc:HGNC:7975]","synonyms":"COUP-TFI,TFCOUP1,TCFCOUP1,SVP44,ERBAL3,EAR-3","biotype":"protein_coding","ncbi_id":"7025","summary":"The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator. The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats. Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS). [provided by RefSeq, Apr 2014]","start":93583337,"end":93594615,"strand":1,"description":"nuclear receptor subfamily 2 group F member 1 [Source:HGNC Symbol;Acc:HGNC:7975]"}, {"versioned_ensembl_gene_id":"ENSG00000257913.2","gene_symbol":"DDN-AS1","gene_name":"DDN and PRKAG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53464]","synonyms":"CAT1507","biotype":"antisense_RNA","ncbi_id":"105369758","summary":null,"start":48998367,"end":49019235,"strand":1,"description":"DDN and PRKAG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53464]"}, {"versioned_ensembl_gene_id":"ENSG00000226625.1","gene_symbol":"RBM17P1","gene_name":"RNA binding motif protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133330","summary":null,"start":39154075,"end":39155479,"strand":1,"description":"RNA binding motif protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50366]"}, {"versioned_ensembl_gene_id":"ENSG00000232629.8","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32756098,"end":32763534,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000214298.3","gene_symbol":"MRPS21P6","gene_name":"mitochondrial ribosomal protein S21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29753]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359770","summary":null,"start":125166677,"end":125166937,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29753]"}, {"versioned_ensembl_gene_id":"ENSG00000241907.1","gene_symbol":"RPS20P4","gene_name":"ribosomal protein S20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10407]","synonyms":"RPS20B","biotype":"processed_pseudogene","ncbi_id":"6226","summary":null,"start":150021567,"end":150021921,"strand":-1,"description":"ribosomal protein S20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10407]"}, {"versioned_ensembl_gene_id":"ENSG00000135956.8","gene_symbol":"TMEM127","gene_name":"transmembrane protein 127 [Source:HGNC Symbol;Acc:HGNC:26038]","synonyms":"FLJ22257,FLJ20507","biotype":"protein_coding","ncbi_id":"55654","summary":"This gene encodes a transmembrane protein with 3 predicted transmembrane domains. The protein is associated with a subpopulation of vesicular organelles corresponding to early endosomal structures, with the Golgi, and with lysosomes, and may participate in protein trafficking between these structures. Mutations in this gene and several other genes cause pheochromocytomas. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Aug 2010]","start":96248516,"end":96265994,"strand":-1,"description":"transmembrane protein 127 [Source:HGNC Symbol;Acc:HGNC:26038]"}, {"versioned_ensembl_gene_id":"ENSG00000211858.1","gene_symbol":"TRAJ31","gene_name":"T-cell receptor alpha joining 31 [Source:HGNC Symbol;Acc:HGNC:12061]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28724","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22510968,"end":22511024,"strand":1,"description":"T-cell receptor alpha joining 31 [Source:HGNC Symbol;Acc:HGNC:12061]"}, {"versioned_ensembl_gene_id":"ENSG00000177202.2","gene_symbol":"SPACA4","gene_name":"sperm acrosome associated 4 [Source:HGNC Symbol;Acc:HGNC:16441]","synonyms":"SAMP14","biotype":"protein_coding","ncbi_id":"171169","summary":null,"start":48606743,"end":48607714,"strand":1,"description":"sperm acrosome associated 4 [Source:HGNC Symbol;Acc:HGNC:16441]"}, {"versioned_ensembl_gene_id":"ENSG00000256358.1","gene_symbol":"AC016489.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64308316,"end":64308690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227297.1","gene_symbol":"AL035541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57599695,"end":57601200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211857.1","gene_symbol":"TRAJ32","gene_name":"T-cell receptor alpha joining 32 [Source:HGNC Symbol;Acc:HGNC:12062]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28723","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22509341,"end":22509406,"strand":1,"description":"T-cell receptor alpha joining 32 [Source:HGNC Symbol;Acc:HGNC:12062]"}, {"versioned_ensembl_gene_id":"ENSG00000226167.1","gene_symbol":"AP4B1-AS1","gene_name":"AP4B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44114]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287722","summary":null,"start":113856635,"end":113901237,"strand":1,"description":"AP4B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44114]"}, {"versioned_ensembl_gene_id":"ENSG00000106078.17","gene_symbol":"COBL","gene_name":"cordon-bleu WH2 repeat protein [Source:HGNC Symbol;Acc:HGNC:22199]","synonyms":"KIAA0633","biotype":"protein_coding","ncbi_id":"23242","summary":"This gene encodes a protein that contains WH2 domains (WASP, Wiskott-Aldrich syndrome protein, homology domain-2) that interact with actin. The encoded actin regulator protein is required for growth and assembly of brush border microvilli that play a role in maintaining intestinal homeostasis. A similar protein in mouse functions in midbrain neural tube closure. A pseudogene of this gene is located on chromosome X. [provided by RefSeq, Oct 2016]","start":51016212,"end":51316818,"strand":-1,"description":"cordon-bleu WH2 repeat protein [Source:HGNC Symbol;Acc:HGNC:22199]"}, {"versioned_ensembl_gene_id":"ENSG00000258807.5","gene_symbol":"AL359237.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87710419,"end":87872291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228204.2","gene_symbol":"AC004830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50866747,"end":51022990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135778.11","gene_symbol":"NTPCR","gene_name":"nucleoside-triphosphatase, cancer-related [Source:HGNC Symbol;Acc:HGNC:28204]","synonyms":"C1orf57,MGC13186,HCR-NTPase","biotype":"protein_coding","ncbi_id":"84284","summary":"The protein encoded by this gene is a non-specific nucleoside triphosphatase that is slow-acting in vitro. This gene is overexpressed in many tumor tissues, and while it is not essential for the cell, overexpression is cytotoxic. However, the cytotoxicity is not related to its triphosphatase activity. [provided by RefSeq, Jul 2016]","start":232950605,"end":232983882,"strand":1,"description":"nucleoside-triphosphatase, cancer-related [Source:HGNC Symbol;Acc:HGNC:28204]"}, {"versioned_ensembl_gene_id":"ENSG00000231940.1","gene_symbol":"RPS7P3","gene_name":"ribosomal protein S7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440732","summary":null,"start":233288868,"end":233289447,"strand":-1,"description":"ribosomal protein S7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36518]"}, {"versioned_ensembl_gene_id":"ENSG00000008196.12","gene_symbol":"TFAP2B","gene_name":"transcription factor AP-2 beta [Source:HGNC Symbol;Acc:HGNC:11743]","synonyms":"AP2-B","biotype":"protein_coding","ncbi_id":"7021","summary":"This gene encodes a member of the AP-2 family of transcription factors. AP-2 proteins form homo- or hetero-dimers with other AP-2 family members and bind specific DNA sequences. They are thought to stimulate cell proliferation and suppress terminal differentiation of specific cell types during embryonic development. Specific AP-2 family members differ in their expression patterns and binding affinity for different promoters. This protein functions as both a transcriptional activator and repressor. Mutations in this gene result in autosomal dominant Char syndrome, suggesting that this gene functions in the differentiation of neural crest cell derivatives. [provided by RefSeq, Jul 2008]","start":50818723,"end":50847613,"strand":1,"description":"transcription factor AP-2 beta [Source:HGNC Symbol;Acc:HGNC:11743]"}, {"versioned_ensembl_gene_id":"ENSG00000165915.13","gene_symbol":"SLC39A13","gene_name":"solute carrier family 39 member 13 [Source:HGNC Symbol;Acc:HGNC:20859]","synonyms":"FLJ25785","biotype":"protein_coding","ncbi_id":"91252","summary":"This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome. Alternate transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":47407132,"end":47416501,"strand":1,"description":"solute carrier family 39 member 13 [Source:HGNC Symbol;Acc:HGNC:20859]"}, {"versioned_ensembl_gene_id":"ENSG00000270361.1","gene_symbol":"AL451085.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154937370,"end":154938059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279610.1","gene_symbol":"C20orf181","gene_name":"chromosome 20 open reading frame 181 [Source:HGNC Symbol;Acc:HGNC:16174]","synonyms":"dJ824A14.1","biotype":"TEC","ncbi_id":"100128998","summary":null,"start":63843436,"end":63843915,"strand":-1,"description":"chromosome 20 open reading frame 181 [Source:HGNC Symbol;Acc:HGNC:16174]"}, {"versioned_ensembl_gene_id":"ENSG00000263412.1","gene_symbol":"AC004477.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48045141,"end":48048073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270554.1","gene_symbol":"AC069431.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182843521,"end":182844619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213448.3","gene_symbol":"RPS23P2","gene_name":"ribosomal protein S23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36568]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391701","summary":null,"start":137448087,"end":137448501,"strand":1,"description":"ribosomal protein S23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36568]"}, {"versioned_ensembl_gene_id":"ENSG00000255121.2","gene_symbol":"AP003392.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118994824,"end":118998004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153714.5","gene_symbol":"LURAP1L","gene_name":"leucine rich adaptor protein 1 like [Source:HGNC Symbol;Acc:HGNC:31452]","synonyms":"MGC46502,FLJ38505,C9orf150,bA3L8.2","biotype":"protein_coding","ncbi_id":"286343","summary":null,"start":12775021,"end":12822131,"strand":1,"description":"leucine rich adaptor protein 1 like [Source:HGNC Symbol;Acc:HGNC:31452]"}, {"versioned_ensembl_gene_id":"ENSG00000256525.6","gene_symbol":"POLG2","gene_name":"DNA polymerase gamma 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9180]","synonyms":"MTPOLB,HP55","biotype":"protein_coding","ncbi_id":"11232","summary":"This gene encodes the processivity subunit of the mitochondrial DNA polymerase gamma. The encoded protein forms a heterotrimer containing one catalytic subunit and two processivity subunits. This protein enhances DNA binding and promotes processive DNA synthesis. Mutations in this gene result in autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions.[provided by RefSeq, Sep 2009]","start":64477785,"end":64497036,"strand":-1,"description":"DNA polymerase gamma 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9180]"}, {"versioned_ensembl_gene_id":"ENSG00000228085.1","gene_symbol":"AC009296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50843578,"end":50843732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272969.1","gene_symbol":"AC024243.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55547112,"end":55547889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242280.1","gene_symbol":"SLC16A1P1","gene_name":"SLC16A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422547","summary":null,"start":143985142,"end":143986651,"strand":1,"description":"SLC16A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48931]"}, {"versioned_ensembl_gene_id":"ENSG00000251567.5","gene_symbol":"AC018680.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136118675,"end":136395471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082213.17","gene_symbol":"C5orf22","gene_name":"chromosome 5 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:25639]","synonyms":"FLJ11193","biotype":"protein_coding","ncbi_id":"55322","summary":null,"start":31532266,"end":31555058,"strand":1,"description":"chromosome 5 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:25639]"}, {"versioned_ensembl_gene_id":"ENSG00000276699.1","gene_symbol":"TRAJ36","gene_name":"T-cell receptor alpha joining 36 [Source:HGNC Symbol;Acc:HGNC:12066]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28719","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22505110,"end":22505167,"strand":1,"description":"T-cell receptor alpha joining 36 [Source:HGNC Symbol;Acc:HGNC:12066]"}, {"versioned_ensembl_gene_id":"ENSG00000272801.1","gene_symbol":"AC004080.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27147366,"end":27152598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146147.14","gene_symbol":"MLIP","gene_name":"muscular LMNA interacting protein [Source:HGNC Symbol;Acc:HGNC:21355]","synonyms":"MGC18257,CIP,C6orf142","biotype":"protein_coding","ncbi_id":"90523","summary":null,"start":53929982,"end":54266280,"strand":1,"description":"muscular LMNA interacting protein [Source:HGNC Symbol;Acc:HGNC:21355]"}, {"versioned_ensembl_gene_id":"ENSG00000224221.1","gene_symbol":"AC019205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73391038,"end":73391767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232175.1","gene_symbol":"AL122003.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":232917235,"end":232918018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164796.17","gene_symbol":"CSMD3","gene_name":"CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:HGNC:19291]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114788","summary":null,"start":112222928,"end":113437099,"strand":-1,"description":"CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:HGNC:19291]"}, {"versioned_ensembl_gene_id":"ENSG00000229214.1","gene_symbol":"LINC00242","gene_name":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]","synonyms":"dJ266L20.5,C6orf122,NCRNA00242,FLJ31451","biotype":"lincRNA","ncbi_id":"401288","summary":null,"start":169788790,"end":169798825,"strand":-1,"description":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]"}, {"versioned_ensembl_gene_id":"ENSG00000236996.1","gene_symbol":"MLIP-IT1","gene_name":"MLIP intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41461]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874282","summary":null,"start":53998890,"end":54007152,"strand":1,"description":"MLIP intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41461]"}, {"versioned_ensembl_gene_id":"ENSG00000106006.6","gene_symbol":"HOXA6","gene_name":"homeobox A6 [Source:HGNC Symbol;Acc:HGNC:5107]","synonyms":"HOX1B,HOX1","biotype":"protein_coding","ncbi_id":"3203","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":27145396,"end":27150603,"strand":-1,"description":"homeobox A6 [Source:HGNC Symbol;Acc:HGNC:5107]"}, {"versioned_ensembl_gene_id":"ENSG00000258730.1","gene_symbol":"ITPK1-AS1","gene_name":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]","synonyms":"C14orf85,NCRNA00203,ITPK1AS,ITPK1-AS","biotype":"antisense_RNA","ncbi_id":"319085","summary":null,"start":93067452,"end":93072152,"strand":1,"description":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]"}, {"versioned_ensembl_gene_id":"ENSG00000271605.5","gene_symbol":"MILR1","gene_name":"mast cell immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:27570]","synonyms":"MCA-32,C17orf60,Allergin-1","biotype":"protein_coding","ncbi_id":"284021","summary":null,"start":64449037,"end":64468643,"strand":1,"description":"mast cell immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:27570]"}, {"versioned_ensembl_gene_id":"ENSG00000197818.11","gene_symbol":"SLC9A8","gene_name":"solute carrier family 9 member A8 [Source:HGNC Symbol;Acc:HGNC:20728]","synonyms":"NHE8,KIAA0939","biotype":"protein_coding","ncbi_id":"23315","summary":"Sodium-hydrogen exchangers (NHEs), such as SLC9A8, are integral transmembrane proteins that exchange extracellular Na+ for intracellular H+. NHEs have multiple functions, including intracellular pH homeostasis, cell volume regulation, and electroneutral NaCl absorption in epithelia (Xu et al., 2008 [PubMed 18209477]).[supplied by OMIM, Apr 2009]","start":49812713,"end":49892242,"strand":1,"description":"solute carrier family 9 member A8 [Source:HGNC Symbol;Acc:HGNC:20728]"}, {"versioned_ensembl_gene_id":"ENSG00000273433.1","gene_symbol":"AC004080.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27128969,"end":27152561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269486.2","gene_symbol":"AC011455.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38935297,"end":38938632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122592.7","gene_symbol":"HOXA7","gene_name":"homeobox A7 [Source:HGNC Symbol;Acc:HGNC:5108]","synonyms":"HOX1A,HOX1","biotype":"protein_coding","ncbi_id":"3204","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. For example, the encoded protein represses the transcription of differentiation-specific genes during keratinocyte proliferation, but this repression is then overcome by differentiation signals. This gene is highly similar to the antennapedia (Antp) gene of Drosophila. [provided by RefSeq, Jul 2008]","start":27153716,"end":27157936,"strand":-1,"description":"homeobox A7 [Source:HGNC Symbol;Acc:HGNC:5108]"}, {"versioned_ensembl_gene_id":"ENSG00000213424.8","gene_symbol":"KRT222","gene_name":"keratin 222 [Source:HGNC Symbol;Acc:HGNC:28695]","synonyms":"MGC45562,KRT222P,KA21","biotype":"protein_coding","ncbi_id":"125113","summary":null,"start":40654665,"end":40665181,"strand":-1,"description":"keratin 222 [Source:HGNC Symbol;Acc:HGNC:28695]"}, {"versioned_ensembl_gene_id":"ENSG00000164334.15","gene_symbol":"FAM170A","gene_name":"family with sequence similarity 170 member A [Source:HGNC Symbol;Acc:HGNC:27963]","synonyms":"ZNFD","biotype":"protein_coding","ncbi_id":"340069","summary":null,"start":119629559,"end":119635822,"strand":1,"description":"family with sequence similarity 170 member A [Source:HGNC Symbol;Acc:HGNC:27963]"}, {"versioned_ensembl_gene_id":"ENSG00000213663.4","gene_symbol":"AC010409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119547131,"end":119547606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105523.3","gene_symbol":"FAM83E","gene_name":"family with sequence similarity 83 member E [Source:HGNC Symbol;Acc:HGNC:25972]","synonyms":"FLJ20200","biotype":"protein_coding","ncbi_id":"54854","summary":null,"start":48600810,"end":48614854,"strand":-1,"description":"family with sequence similarity 83 member E [Source:HGNC Symbol;Acc:HGNC:25972]"}, {"versioned_ensembl_gene_id":"ENSG00000105538.9","gene_symbol":"RASIP1","gene_name":"Ras interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24716]","synonyms":"FLJ20401,RAIN","biotype":"protein_coding","ncbi_id":"54922","summary":null,"start":48720587,"end":48740721,"strand":-1,"description":"Ras interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24716]"}, {"versioned_ensembl_gene_id":"ENSG00000080007.7","gene_symbol":"DDX43","gene_name":"DEAD-box helicase 43 [Source:HGNC Symbol;Acc:HGNC:18677]","synonyms":"CT13,HAGE,DKFZp434H2114","biotype":"protein_coding","ncbi_id":"55510","summary":" The protein encoded by this gene is an ATP-dependent RNA helicase in the DEAD-box family and displays tumor-specific expression. [provided by RefSeq, Jul 2008]","start":73394748,"end":73417569,"strand":1,"description":"DEAD-box helicase 43 [Source:HGNC Symbol;Acc:HGNC:18677]"}, {"versioned_ensembl_gene_id":"ENSG00000232022.7","gene_symbol":"FAAHP1","gene_name":"fatty acid amide hydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50679]","synonyms":"LINC00505","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729041","summary":null,"start":46432129,"end":46482493,"strand":1,"description":"fatty acid amide hydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50679]"}, {"versioned_ensembl_gene_id":"ENSG00000232855.6","gene_symbol":"AF165147.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28439346,"end":28674848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100225.17","gene_symbol":"FBXO7","gene_name":"F-box protein 7 [Source:HGNC Symbol;Acc:HGNC:13586]","synonyms":"PARK15,FBX7,Fbx","biotype":"protein_coding","ncbi_id":"25793","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it may play a role in regulation of hematopoiesis. Alternatively spliced transcript variants of this gene have been identified with the full-length natures of only some variants being determined. [provided by RefSeq, Jul 2008]","start":32474676,"end":32498829,"strand":1,"description":"F-box protein 7 [Source:HGNC Symbol;Acc:HGNC:13586]"}, {"versioned_ensembl_gene_id":"ENSG00000160695.14","gene_symbol":"VPS11","gene_name":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]","synonyms":"RNF108,PEP5","biotype":"protein_coding","ncbi_id":"55823","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps11 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":119067692,"end":119081978,"strand":1,"description":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]"}, {"versioned_ensembl_gene_id":"ENSG00000166167.17","gene_symbol":"BTRC","gene_name":"beta-transducin repeat containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:1144]","synonyms":"Fwd1,FBXW1A,bTrCP1,bTrCP,betaTrCP,beta-TrCP1","biotype":"protein_coding","ncbi_id":"8945","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbws class; in addition to an F-box, this protein contains multiple WD-40 repeats. The encoded protein mediates degradation of CD4 via its interaction with HIV-1 Vpu. It has also been shown to ubiquitinate phosphorylated NFKBIA (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha), targeting it for degradation and thus activating nuclear factor kappa-B. Alternatively spliced transcript variants have been described. A related pseudogene exists in chromosome 6. [provided by RefSeq, Mar 2012]","start":101354033,"end":101557321,"strand":1,"description":"beta-transducin repeat containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:1144]"}, {"versioned_ensembl_gene_id":"ENSG00000058063.15","gene_symbol":"ATP11B","gene_name":"ATPase phospholipid transporting 11B (putative) [Source:HGNC Symbol;Acc:HGNC:13553]","synonyms":"KIAA0956,ATPIR,ATPIF","biotype":"protein_coding","ncbi_id":"23200","summary":"P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005]","start":182793500,"end":182921635,"strand":1,"description":"ATPase phospholipid transporting 11B (putative) [Source:HGNC Symbol;Acc:HGNC:13553]"}, {"versioned_ensembl_gene_id":"ENSG00000243468.5","gene_symbol":"INGX","gene_name":"inhibitor of growth family, X-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:6064]","synonyms":"ING2,ING1-like","biotype":"transcribed_processed_pseudogene","ncbi_id":"27160","summary":null,"start":71491682,"end":71492928,"strand":-1,"description":"inhibitor of growth family, X-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:6064]"}, {"versioned_ensembl_gene_id":"ENSG00000213018.2","gene_symbol":"AL590762.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71420083,"end":71420514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248884.1","gene_symbol":"AC010280.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68430427,"end":68434481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271751.1","gene_symbol":"AP003392.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119065263,"end":119065677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181418.7","gene_symbol":"DDN","gene_name":"dendrin [Source:HGNC Symbol;Acc:HGNC:24458]","synonyms":"KIAA0749","biotype":"protein_coding","ncbi_id":"23109","summary":null,"start":48995149,"end":48999309,"strand":-1,"description":"dendrin [Source:HGNC Symbol;Acc:HGNC:24458]"}, {"versioned_ensembl_gene_id":"ENSG00000160131.13","gene_symbol":"VMA21","gene_name":"VMA21, vacuolar ATPase assembly factor [Source:HGNC Symbol;Acc:HGNC:22082]","synonyms":"XMEA,MEAX","biotype":"protein_coding","ncbi_id":"203547","summary":"This gene encodes a chaperone for assembly of lysosomal vacuolar ATPase.[provided by RefSeq, Jul 2012]","start":151396515,"end":151409364,"strand":1,"description":"VMA21, vacuolar ATPase assembly factor [Source:HGNC Symbol;Acc:HGNC:22082]"}, {"versioned_ensembl_gene_id":"ENSG00000226766.1","gene_symbol":"FABP7P1","gene_name":"fatty acid binding protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506953","summary":null,"start":243624666,"end":243625056,"strand":-1,"description":"fatty acid binding protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41951]"}, {"versioned_ensembl_gene_id":"ENSG00000101294.16","gene_symbol":"HM13","gene_name":"histocompatibility minor 13 [Source:HGNC Symbol;Acc:HGNC:16435]","synonyms":"IMP1,H13,dJ324O17.1,SPPL1,SPP,PSL3,PSENL3,IMPAS","biotype":"protein_coding","ncbi_id":"81502","summary":"The protein encoded by this gene, which localizes to the endoplasmic reticulum, catalyzes intramembrane proteolysis of some signal peptides after they have been cleaved from a preprotein. This activity is required to generate signal sequence-derived human lymphocyte antigen-E epitopes that are recognized by the immune system, and to process hepatitis C virus core protein. The encoded protein is an integral membrane protein with sequence motifs characteristic of the presenilin-type aspartic proteases. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31514428,"end":31577923,"strand":1,"description":"histocompatibility minor 13 [Source:HGNC Symbol;Acc:HGNC:16435]"}, {"versioned_ensembl_gene_id":"ENSG00000235262.1","gene_symbol":"KDM5C-IT1","gene_name":"KDM5C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41384]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874299","summary":null,"start":53212408,"end":53214679,"strand":-1,"description":"KDM5C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41384]"}, {"versioned_ensembl_gene_id":"ENSG00000152402.10","gene_symbol":"GUCY1A2","gene_name":"guanylate cyclase 1 soluble subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4684]","synonyms":"GUC1A2,GC-SA2","biotype":"protein_coding","ncbi_id":"2977","summary":"Soluble guanylate cyclases are heterodimeric proteins that catalyze the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. The protein encoded by this gene is an alpha subunit of this complex and it interacts with a beta subunit to form the guanylate cyclase enzyme, which is activated by nitric oxide. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":106674012,"end":107018524,"strand":-1,"description":"guanylate cyclase 1 soluble subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4684]"}, {"versioned_ensembl_gene_id":"ENSG00000102195.9","gene_symbol":"GPR50","gene_name":"G protein-coupled receptor 50 [Source:HGNC Symbol;Acc:HGNC:4506]","synonyms":"Mel1c,H9","biotype":"protein_coding","ncbi_id":"9248","summary":"This gene product belongs to the G-protein coupled receptor 1 family. Even though this protein shares similarity with the melatonin receptors, it does not bind melatonin, however, it inhibits melatonin receptor 1A function through heterodimerization. Polymorphic variants of this gene have been associated with bipolar affective disorder in women. [provided by RefSeq, Jan 2010]","start":151176653,"end":151181465,"strand":1,"description":"G protein-coupled receptor 50 [Source:HGNC Symbol;Acc:HGNC:4506]"}, {"versioned_ensembl_gene_id":"ENSG00000202259.1","gene_symbol":"RNU6-1318P","gene_name":"RNA, U6 small nuclear 1318, pseudogene [Source:HGNC Symbol;Acc:HGNC:48281]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480141","summary":null,"start":100000637,"end":100000739,"strand":-1,"description":"RNA, U6 small nuclear 1318, pseudogene [Source:HGNC Symbol;Acc:HGNC:48281]"}, {"versioned_ensembl_gene_id":"ENSG00000211850.1","gene_symbol":"TRAJ39","gene_name":"T-cell receptor alpha joining 39 [Source:HGNC Symbol;Acc:HGNC:12069]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28716","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22501601,"end":22501663,"strand":1,"description":"T-cell receptor alpha joining 39 [Source:HGNC Symbol;Acc:HGNC:12069]"}, {"versioned_ensembl_gene_id":"ENSG00000211849.1","gene_symbol":"TRAJ40","gene_name":"T-cell receptor alpha joining 40 [Source:HGNC Symbol;Acc:HGNC:12071]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28715","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22499689,"end":22499749,"strand":1,"description":"T-cell receptor alpha joining 40 [Source:HGNC Symbol;Acc:HGNC:12071]"}, {"versioned_ensembl_gene_id":"ENSG00000250813.1","gene_symbol":"SERF1AP1","gene_name":"small EDRK-rich factor 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44061]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131921","summary":null,"start":137301001,"end":137301187,"strand":-1,"description":"small EDRK-rich factor 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44061]"}, {"versioned_ensembl_gene_id":"ENSG00000152034.10","gene_symbol":"MCHR2","gene_name":"melanin concentrating hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:20867]","synonyms":"SLT,MCH2R,MCH2,GPR145","biotype":"protein_coding","ncbi_id":"84539","summary":null,"start":99919910,"end":99994247,"strand":-1,"description":"melanin concentrating hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:20867]"}, {"versioned_ensembl_gene_id":"ENSG00000172985.10","gene_symbol":"SH3RF3","gene_name":"SH3 domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:24699]","synonyms":"SH3MD4,POSH2,FLJ00204","biotype":"protein_coding","ncbi_id":"344558","summary":null,"start":109129348,"end":109504632,"strand":1,"description":"SH3 domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:24699]"}, {"versioned_ensembl_gene_id":"ENSG00000254463.1","gene_symbol":"AC087276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43466392,"end":43466871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254907.1","gene_symbol":"AC087276.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43328748,"end":43359296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000097021.19","gene_symbol":"ACOT7","gene_name":"acyl-CoA thioesterase 7 [Source:HGNC Symbol;Acc:HGNC:24157]","synonyms":"MGC1126,LACH1,hBACH,CTE-II,BACH,ACT,ACH1","biotype":"protein_coding","ncbi_id":"11332","summary":"This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008]","start":6264269,"end":6394391,"strand":-1,"description":"acyl-CoA thioesterase 7 [Source:HGNC Symbol;Acc:HGNC:24157]"}, {"versioned_ensembl_gene_id":"ENSG00000254661.2","gene_symbol":"AC009869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15910957,"end":15927443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219257.2","gene_symbol":"NPM1P38","gene_name":"nucleophosmin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45217]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128985","summary":null,"start":100050372,"end":100051236,"strand":-1,"description":"nucleophosmin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:45217]"}, {"versioned_ensembl_gene_id":"ENSG00000276701.2","gene_symbol":"MIF","gene_name":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]","synonyms":"GLIF,GIF","biotype":"protein_coding","ncbi_id":"4282","summary":"This gene encodes a lymphokine involved in cell-mediated immunity, immunoregulation, and inflammation. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. This lymphokine and the JAB1 protein form a complex in the cytosol near the peripheral plasma membrane, which may indicate an additional role in integrin signaling pathways. [provided by RefSeq, Jul 2008]","start":23894004,"end":23895227,"strand":1,"description":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]"}, {"versioned_ensembl_gene_id":"ENSG00000273377.1","gene_symbol":"AC004853.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143980905,"end":143981820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254695.1","gene_symbol":"AC087379.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15643885,"end":15705368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106829.18","gene_symbol":"TLE4","gene_name":"transducin like enhancer of split 4 [Source:HGNC Symbol;Acc:HGNC:11840]","synonyms":"GRG4,ESG,E(spI)","biotype":"protein_coding","ncbi_id":"7091","summary":null,"start":79571773,"end":79726882,"strand":1,"description":"transducin like enhancer of split 4 [Source:HGNC Symbol;Acc:HGNC:11840]"}, {"versioned_ensembl_gene_id":"ENSG00000203908.3","gene_symbol":"KHDC3L","gene_name":"KH domain containing 3 like, subcortical maternal complex member [Source:HGNC Symbol;Acc:HGNC:33699]","synonyms":"ECAT1,C6orf221","biotype":"protein_coding","ncbi_id":"154288","summary":"The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011]","start":73362677,"end":73364171,"strand":1,"description":"KH domain containing 3 like, subcortical maternal complex member [Source:HGNC Symbol;Acc:HGNC:33699]"}, {"versioned_ensembl_gene_id":"ENSG00000269667.1","gene_symbol":"AC092723.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85981750,"end":85984723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158201.9","gene_symbol":"ABHD3","gene_name":"abhydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18718]","synonyms":"LABH3","biotype":"protein_coding","ncbi_id":"171586","summary":"This gene encodes a protein containing an alpha/beta hydrolase fold, which is a catalytic domain found in a very wide range of enzymes. The function of this protein has not been determined. [provided by RefSeq, Jul 2008]","start":21650897,"end":21704805,"strand":-1,"description":"abhydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18718]"}, {"versioned_ensembl_gene_id":"ENSG00000132915.10","gene_symbol":"PDE6A","gene_name":"phosphodiesterase 6A [Source:HGNC Symbol;Acc:HGNC:8785]","synonyms":"RP43,PDEA","biotype":"protein_coding","ncbi_id":"5145","summary":"This gene encodes the cyclic-GMP (cGMP)-specific phosphodiesterase 6A alpha subunit, expressed in cells of the retinal rod outer segment. The phosphodiesterase 6 holoenzyme is a heterotrimer composed of an alpha, beta, and two gamma subunits. cGMP is an important regulator of rod cell membrane current, and its dynamic concentration is established by phosphodiesterase 6A cGMP hydrolysis and guanylate cyclase cGMP synthesis. The protein is a subunit of a key phototransduction enzyme and participates in processes of transmission and amplification of the visual signal. Mutations in this gene have been identified as one cause of autosomal recessive retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":149857955,"end":149944793,"strand":-1,"description":"phosphodiesterase 6A [Source:HGNC Symbol;Acc:HGNC:8785]"}, {"versioned_ensembl_gene_id":"ENSG00000270916.1","gene_symbol":"RPL12P50","gene_name":"ribosomal protein L12 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:51942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075212","summary":null,"start":151023607,"end":151023722,"strand":-1,"description":"ribosomal protein L12 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:51942]"}, {"versioned_ensembl_gene_id":"ENSG00000254146.1","gene_symbol":"HMGB1P46","gene_name":"high mobility group box 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39279]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419978","summary":null,"start":107173200,"end":107173809,"strand":-1,"description":"high mobility group box 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39279]"}, {"versioned_ensembl_gene_id":"ENSG00000218521.1","gene_symbol":"AL589655.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38002832,"end":38003313,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143321.18","gene_symbol":"HDGF","gene_name":"heparin binding growth factor [Source:HGNC Symbol;Acc:HGNC:4856]","synonyms":"HMG1L2","biotype":"protein_coding","ncbi_id":"3068","summary":"This gene encodes a member of the hepatoma-derived growth factor family. The encoded protein has mitogenic and DNA-binding activity and may play a role in cellular proliferation and differentiation. High levels of expression of this gene enhance the growth of many tumors. This gene was thought initially to be located on chromosome X; however, that location has been determined to correspond to a related pseudogene. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2016]","start":156742107,"end":156766925,"strand":-1,"description":"heparin binding growth factor [Source:HGNC Symbol;Acc:HGNC:4856]"}, {"versioned_ensembl_gene_id":"ENSG00000214252.4","gene_symbol":"AZGP1P2","gene_name":"alpha-2-glycoprotein 1, zinc-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:912]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401393","summary":null,"start":101287482,"end":101289771,"strand":-1,"description":"alpha-2-glycoprotein 1, zinc-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:912]"}, {"versioned_ensembl_gene_id":"ENSG00000278683.1","gene_symbol":"AC006329.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101273322,"end":101273715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140287.10","gene_symbol":"HDC","gene_name":"histidine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3067","summary":"This gene encodes a member of the group II decarboxylase family and forms a homodimer that converts L-histidine to histamine in a pyridoxal phosphate dependent manner. Histamine regulates several physiologic processes, including neurotransmission, gastric acid secretion,inflamation, and smooth muscle tone.[provided by RefSeq, Aug 2010]","start":50241947,"end":50266026,"strand":-1,"description":"histidine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4855]"}, {"versioned_ensembl_gene_id":"ENSG00000183311.16","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30709720,"end":30714946,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000132465.10","gene_symbol":"JCHAIN","gene_name":"joining chain of multimeric IgA and IgM [Source:HGNC Symbol;Acc:HGNC:5713]","synonyms":"JCH,IGJ,IGCJ","biotype":"protein_coding","ncbi_id":"3512","summary":null,"start":70655541,"end":70681817,"strand":-1,"description":"joining chain of multimeric IgA and IgM [Source:HGNC Symbol;Acc:HGNC:5713]"}, {"versioned_ensembl_gene_id":"ENSG00000259019.1","gene_symbol":"EIF4BP1","gene_name":"eukaryotic translation initiation factor 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19929]","synonyms":"EIF4BP","biotype":"transcribed_processed_pseudogene","ncbi_id":"319118","summary":null,"start":44077534,"end":44077884,"strand":-1,"description":"eukaryotic translation initiation factor 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19929]"}, {"versioned_ensembl_gene_id":"ENSG00000259137.1","gene_symbol":"AL109766.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44120210,"end":44120761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259148.1","gene_symbol":"YWHAZP1","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19938]","synonyms":"YWHAZP","biotype":"processed_pseudogene","ncbi_id":"319120","summary":null,"start":44290997,"end":44291718,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19938]"}, {"versioned_ensembl_gene_id":"ENSG00000276257.1","gene_symbol":"AL513478.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66084804,"end":66085031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259028.1","gene_symbol":"AL135746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87568181,"end":87569399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258958.1","gene_symbol":"AL157688.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87323753,"end":87332390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100532.11","gene_symbol":"CGRRF1","gene_name":"cell growth regulator with ring finger domain 1 [Source:HGNC Symbol;Acc:HGNC:15528]","synonyms":"RNF197,CGR19","biotype":"protein_coding","ncbi_id":"10668","summary":null,"start":54509812,"end":54539309,"strand":1,"description":"cell growth regulator with ring finger domain 1 [Source:HGNC Symbol;Acc:HGNC:15528]"}, {"versioned_ensembl_gene_id":"ENSG00000258804.1","gene_symbol":"LINC01148","gene_name":"long intergenic non-protein coding RNA 1148 [Source:HGNC Symbol;Acc:HGNC:27507]","synonyms":"LOC283585","biotype":"lincRNA","ncbi_id":"283585","summary":null,"start":86905778,"end":86922755,"strand":1,"description":"long intergenic non-protein coding RNA 1148 [Source:HGNC Symbol;Acc:HGNC:27507]"}, {"versioned_ensembl_gene_id":"ENSG00000258994.1","gene_symbol":"LINC02309","gene_name":"long intergenic non-protein coding RNA 2309 [Source:HGNC Symbol;Acc:HGNC:53228]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370607","summary":null,"start":86332376,"end":86401285,"strand":1,"description":"long intergenic non-protein coding RNA 2309 [Source:HGNC Symbol;Acc:HGNC:53228]"}, {"versioned_ensembl_gene_id":"ENSG00000136908.17","gene_symbol":"DPM2","gene_name":"dolichyl-phosphate mannosyltransferase subunit 2, regulatory [Source:HGNC Symbol;Acc:HGNC:3006]","synonyms":"MGC111193,MGC21559","biotype":"protein_coding","ncbi_id":"8818","summary":"Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. The protein encoded by this gene is a hydrophobic protein that contains 2 predicted transmembrane domains and a putative ER localization signal near the C terminus. This protein associates with DPM1 in vivo and is required for the ER localization and stable expression of DPM1 and also enhances the binding of dolichol-phosphate to DPM1. [provided by RefSeq, Jul 2008]","start":127935099,"end":127938484,"strand":-1,"description":"dolichyl-phosphate mannosyltransferase subunit 2, regulatory [Source:HGNC Symbol;Acc:HGNC:3006]"}, {"versioned_ensembl_gene_id":"ENSG00000225125.2","gene_symbol":"RANP4","gene_name":"RAN, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39859]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130621","summary":null,"start":136807223,"end":136807877,"strand":-1,"description":"RAN, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39859]"}, {"versioned_ensembl_gene_id":"ENSG00000253877.5","gene_symbol":"LINC01608","gene_name":"long intergenic non-protein coding RNA 1608 [Source:HGNC Symbol;Acc:HGNC:51662]","synonyms":"TCONS_00015136","biotype":"lincRNA","ncbi_id":"101927459","summary":null,"start":110937690,"end":111027433,"strand":-1,"description":"long intergenic non-protein coding RNA 1608 [Source:HGNC Symbol;Acc:HGNC:51662]"}, {"versioned_ensembl_gene_id":"ENSG00000270105.1","gene_symbol":"AC136475.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":322186,"end":322727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124193.14","gene_symbol":"SRSF6","gene_name":"serine and arginine rich splicing factor 6 [Source:HGNC Symbol;Acc:HGNC:10788]","synonyms":"SRP55,SFRS6,B52","biotype":"protein_coding","ncbi_id":"6431","summary":"The protein encoded by this gene is involved in mRNA splicing and may play a role in the determination of alternative splicing. The encoded nuclear protein belongs to the splicing factor SR family and has been shown to bind with and modulate another member of the family, SFRS12. Alternative splicing results in multiple transcript variants. In addition, two pseudogenes, one on chromosome 17 and the other on the X chromosome, have been found for this gene.[provided by RefSeq, Sep 2010]","start":43457928,"end":43464247,"strand":1,"description":"serine and arginine rich splicing factor 6 [Source:HGNC Symbol;Acc:HGNC:10788]"}, {"versioned_ensembl_gene_id":"ENSG00000236799.1","gene_symbol":"AL355340.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114994657,"end":114996593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117020.16","gene_symbol":"AKT3","gene_name":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]","synonyms":"RAC-gamma,PRKBG,PKBG","biotype":"protein_coding","ncbi_id":"10000","summary":"The protein encoded by this gene is a member of the AKT, also called PKB, serine/threonine protein kinase family. AKT kinases are known to be regulators of cell signaling in response to insulin and growth factors. They are involved in a wide variety of biological processes including cell proliferation, differentiation, apoptosis, tumorigenesis, as well as glycogen synthesis and glucose uptake. This kinase has been shown to be stimulated by platelet-derived growth factor (PDGF), insulin, and insulin-like growth factor 1 (IGF1). Alternatively splice transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":243488233,"end":243851079,"strand":-1,"description":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]"}, {"versioned_ensembl_gene_id":"ENSG00000268614.1","gene_symbol":"AC008878.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7533595,"end":7540059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143294.14","gene_symbol":"PRCC","gene_name":"papillary renal cell carcinoma (translocation-associated) [Source:HGNC Symbol;Acc:HGNC:9343]","synonyms":"RCCP1","biotype":"protein_coding","ncbi_id":"5546","summary":"This gene encodes a protein that may play a role in pre-mRNA splicing. Chromosomal translocations (X;1)(p11;q21) that result in fusion of this gene to TFE3 (GeneID 7030) have been associated with papillary renal cell carcinoma. A PRCC-TFE3 fusion protein is expressed in affected carcinomas and is likely associated with altered gene transactivation. This fusion protein has also been associated with disruption of the cell cycle.[provided by RefSeq, Aug 2010]","start":156750610,"end":156800817,"strand":1,"description":"papillary renal cell carcinoma (translocation-associated) [Source:HGNC Symbol;Acc:HGNC:9343]"}, {"versioned_ensembl_gene_id":"ENSG00000092969.11","gene_symbol":"TGFB2","gene_name":"transforming growth factor beta 2 [Source:HGNC Symbol;Acc:HGNC:11768]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7042","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGF-beta family members. Disruption of the TGF-beta/SMAD pathway has been implicated in a variety of human cancers. A chromosomal translocation that includes this gene is associated with Peters' anomaly, a congenital defect of the anterior chamber of the eye. Mutations in this gene may be associated with Loeys-Dietz syndrome. This gene encodes multiple isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]","start":218346235,"end":218444619,"strand":1,"description":"transforming growth factor beta 2 [Source:HGNC Symbol;Acc:HGNC:11768]"}, {"versioned_ensembl_gene_id":"ENSG00000223389.1","gene_symbol":"SDCBP2P1","gene_name":"syndecan binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44685]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480801","summary":null,"start":73322837,"end":73323450,"strand":1,"description":"syndecan binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44685]"}, {"versioned_ensembl_gene_id":"ENSG00000228890.1","gene_symbol":"TTTY21","gene_name":"testis-specific transcript, Y-linked 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18845]","synonyms":"NCRNA00146","biotype":"lincRNA","ncbi_id":"252953","summary":null,"start":9717653,"end":9721296,"strand":-1,"description":"testis-specific transcript, Y-linked 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18845]"}, {"versioned_ensembl_gene_id":"ENSG00000259986.1","gene_symbol":"AC103876.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83179182,"end":83439445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235531.9","gene_symbol":"MSC-AS1","gene_name":"MSC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48724]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132891","summary":null,"start":71828167,"end":72118393,"strand":1,"description":"MSC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48724]"}, {"versioned_ensembl_gene_id":"ENSG00000241607.1","gene_symbol":"AC245096.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37441523,"end":37442068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102921.7","gene_symbol":"N4BP1","gene_name":"NEDD4 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29850]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9683","summary":null,"start":48538726,"end":48620148,"strand":-1,"description":"NEDD4 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29850]"}, {"versioned_ensembl_gene_id":"ENSG00000105697.7","gene_symbol":"HAMP","gene_name":"hepcidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:15598]","synonyms":"LEAP1,LEAP-1,HFE2B,HEPC","biotype":"protein_coding","ncbi_id":"57817","summary":"The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity against bacteria and fungi. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Oct 2014]","start":35280716,"end":35285143,"strand":1,"description":"hepcidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:15598]"}, {"versioned_ensembl_gene_id":"ENSG00000259044.1","gene_symbol":"AL357172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85202849,"end":85239474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243696.4","gene_symbol":"AC006254.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52813282,"end":52835729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160633.12","gene_symbol":"SAFB","gene_name":"scaffold attachment factor B [Source:HGNC Symbol;Acc:HGNC:10520]","synonyms":"SAFB1,HET","biotype":"protein_coding","ncbi_id":"6294","summary":"This gene encodes a DNA-binding protein which has high specificity for scaffold or matrix attachment region DNA elements (S/MAR DNA). This protein is thought to be involved in attaching the base of chromatin loops to the nuclear matrix but there is conflicting evidence as to whether this protein is a component of chromatin or a nuclear matrix protein. Scaffold attachment factors are a specific subset of nuclear matrix proteins (NMP) that specifically bind to S/MAR. The encoded protein is thought to serve as a molecular base to assemble a 'transcriptosome complex' in the vicinity of actively transcribed genes. It is involved in the regulation of heat shock protein 27 transcription, can act as an estrogen receptor co-repressor and is a candidate for breast tumorigenesis. This gene is arranged head-to-head with a similar gene whose product has the same functions. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]","start":5623035,"end":5668478,"strand":1,"description":"scaffold attachment factor B [Source:HGNC Symbol;Acc:HGNC:10520]"}, {"versioned_ensembl_gene_id":"ENSG00000227988.1","gene_symbol":"TDGF1P1","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421177","summary":null,"start":38395369,"end":38395895,"strand":-1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42350]"}, {"versioned_ensembl_gene_id":"ENSG00000254241.1","gene_symbol":"MTCO1P47","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:52112]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075284","summary":null,"start":110933263,"end":110934533,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:52112]"}, {"versioned_ensembl_gene_id":"ENSG00000036565.14","gene_symbol":"SLC18A1","gene_name":"solute carrier family 18 member A1 [Source:HGNC Symbol;Acc:HGNC:10934]","synonyms":"CGAT,VMAT1,VAT1","biotype":"protein_coding","ncbi_id":"6570","summary":"The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]","start":20144855,"end":20183206,"strand":-1,"description":"solute carrier family 18 member A1 [Source:HGNC Symbol;Acc:HGNC:10934]"}, {"versioned_ensembl_gene_id":"ENSG00000008197.4","gene_symbol":"TFAP2D","gene_name":"transcription factor AP-2 delta [Source:HGNC Symbol;Acc:HGNC:15581]","synonyms":"TFAP2BL1","biotype":"protein_coding","ncbi_id":"83741","summary":null,"start":50713828,"end":50772988,"strand":1,"description":"transcription factor AP-2 delta [Source:HGNC Symbol;Acc:HGNC:15581]"}, {"versioned_ensembl_gene_id":"ENSG00000255923.1","gene_symbol":"AC078878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126864465,"end":126865422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229321.1","gene_symbol":"AC008269.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206866795,"end":206868289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227899.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30692588,"end":30702703,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000212930.3","gene_symbol":"AC093281.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91223419,"end":91223967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174744.13","gene_symbol":"BRMS1","gene_name":"breast cancer metastasis suppressor 1 [Source:HGNC Symbol;Acc:HGNC:17262]","synonyms":"DKFZP564A063","biotype":"protein_coding","ncbi_id":"25855","summary":"This gene reduces the metastatic potential, but not the tumorogenicity, of human breast cancer and melanoma cell lines. The protein encoded by this gene localizes primarily to the nucleus and is a component of the mSin3a family of histone deacetylase complexes (HDAC). The protein contains two coiled-coil motifs and several imperfect leucine zipper motifs. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":66337333,"end":66345125,"strand":-1,"description":"breast cancer metastasis suppressor 1 [Source:HGNC Symbol;Acc:HGNC:17262]"}, {"versioned_ensembl_gene_id":"ENSG00000261244.1","gene_symbol":"AC104758.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77916522,"end":77922019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110375.2","gene_symbol":"UPK2","gene_name":"uroplakin 2 [Source:HGNC Symbol;Acc:HGNC:12579]","synonyms":"UPII,UP2,MGC138598","biotype":"protein_coding","ncbi_id":"7379","summary":"This gene encodes one of the proteins of the highly conserved urothelium-specific integral membrane proteins of the asymmetric unit membrane which forms urothelium apical plaques in mammals. The asymmetric unit membrane is believed to strengthen the urothelium by preventing cell rupture during bladder distention. The encoded protein is expressed in the peripheral blood of bladder cancer patients with transitional cell carcinomas.[provided by RefSeq, Sep 2009]","start":118925164,"end":118958559,"strand":1,"description":"uroplakin 2 [Source:HGNC Symbol;Acc:HGNC:12579]"}, {"versioned_ensembl_gene_id":"ENSG00000254756.1","gene_symbol":"AP001107.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66334494,"end":66339875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279108.1","gene_symbol":"AC008537.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40840159,"end":40842039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275489.1","gene_symbol":"C17orf98","gene_name":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]","synonyms":"LOC388381","biotype":"protein_coding","ncbi_id":"388381","summary":null,"start":38835088,"end":38841455,"strand":-1,"description":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]"}, {"versioned_ensembl_gene_id":"ENSG00000188886.3","gene_symbol":"ASTL","gene_name":"astacin like metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:31704]","synonyms":"SAS1B,ovastacin","biotype":"protein_coding","ncbi_id":"431705","summary":null,"start":96123850,"end":96138436,"strand":-1,"description":"astacin like metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:31704]"}, {"versioned_ensembl_gene_id":"ENSG00000198420.9","gene_symbol":"TCAF1","gene_name":"TRPM8 channel associated factor 1 [Source:HGNC Symbol;Acc:HGNC:22201]","synonyms":"FAM115A,KIAA0738","biotype":"protein_coding","ncbi_id":"9747","summary":null,"start":143851375,"end":143902198,"strand":-1,"description":"TRPM8 channel associated factor 1 [Source:HGNC Symbol;Acc:HGNC:22201]"}, {"versioned_ensembl_gene_id":"ENSG00000235801.1","gene_symbol":"BX927220.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30560894,"end":30563845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254914.1","gene_symbol":"AC109810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42939775,"end":42939998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267751.5","gene_symbol":"AC009005.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":567210,"end":572228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198816.6","gene_symbol":"ZNF358","gene_name":"zinc finger protein 358 [Source:HGNC Symbol;Acc:HGNC:16838]","synonyms":"ZFEND,FLJ10390","biotype":"protein_coding","ncbi_id":"140467","summary":null,"start":7515292,"end":7521026,"strand":1,"description":"zinc finger protein 358 [Source:HGNC Symbol;Acc:HGNC:16838]"}, {"versioned_ensembl_gene_id":"ENSG00000226819.1","gene_symbol":"MEIS1-AS3","gene_name":"MEIS1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40369]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"730198","summary":null,"start":66426735,"end":66433470,"strand":-1,"description":"MEIS1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40369]"}, {"versioned_ensembl_gene_id":"ENSG00000230379.5","gene_symbol":"AP000146.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24938431,"end":24992817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211835.1","gene_symbol":"TRAJ56","gene_name":"T-cell receptor alpha joining 56 [Source:HGNC Symbol;Acc:HGNC:12088]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28699","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22479521,"end":22479582,"strand":1,"description":"T-cell receptor alpha joining 56 [Source:HGNC Symbol;Acc:HGNC:12088]"}, {"versioned_ensembl_gene_id":"ENSG00000130772.13","gene_symbol":"MED18","gene_name":"mediator complex subunit 18 [Source:HGNC Symbol;Acc:HGNC:25944]","synonyms":"p28b,FLJ20045,SRB5","biotype":"protein_coding","ncbi_id":"54797","summary":"MED18 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008]","start":28329002,"end":28335967,"strand":1,"description":"mediator complex subunit 18 [Source:HGNC Symbol;Acc:HGNC:25944]"}, {"versioned_ensembl_gene_id":"ENSG00000235619.1","gene_symbol":"RPL36AP33","gene_name":"ribosomal protein L36a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36475]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100191039","summary":null,"start":35507564,"end":35507873,"strand":1,"description":"ribosomal protein L36a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36475]"}, {"versioned_ensembl_gene_id":"ENSG00000271182.1","gene_symbol":"AC123912.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21634833,"end":21635175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266184.1","gene_symbol":"AC018371.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26831520,"end":26832432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263846.1","gene_symbol":"CIAPIN1P","gene_name":"cytokine induced apoptosis inhibitor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31087]","synonyms":"HsT2384","biotype":"processed_pseudogene","ncbi_id":"728599","summary":null,"start":26599408,"end":26600338,"strand":1,"description":"cytokine induced apoptosis inhibitor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31087]"}, {"versioned_ensembl_gene_id":"ENSG00000228370.1","gene_symbol":"BX927133.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497042,"end":29510088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184903.9","gene_symbol":"IMMP2L","gene_name":"inner mitochondrial membrane peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:14598]","synonyms":"IMMP2L-IT1,IMP2","biotype":"protein_coding","ncbi_id":"83943","summary":"This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for this gene. [provided by RefSeq, Sep 2011]","start":110663051,"end":111562517,"strand":-1,"description":"inner mitochondrial membrane peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:14598]"}, {"versioned_ensembl_gene_id":"ENSG00000124772.11","gene_symbol":"CPNE5","gene_name":"copine 5 [Source:HGNC Symbol;Acc:HGNC:2318]","synonyms":"KIAA1599,CPN5,COPN5","biotype":"protein_coding","ncbi_id":"57699","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene is one of several genes that encode a calcium-dependent protein containing two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. More variants may exist, but their full-length natures could not be determined. [provided by RefSeq, Sep 2015]","start":36740775,"end":36840002,"strand":-1,"description":"copine 5 [Source:HGNC Symbol;Acc:HGNC:2318]"}, {"versioned_ensembl_gene_id":"ENSG00000259035.1","gene_symbol":"AL355838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81741002,"end":82030349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173114.12","gene_symbol":"LRRN3","gene_name":"leucine rich repeat neuronal 3 [Source:HGNC Symbol;Acc:HGNC:17200]","synonyms":"NLRR3,FLJ11129,FIGLER5","biotype":"protein_coding","ncbi_id":"54674","summary":null,"start":111091006,"end":111125454,"strand":1,"description":"leucine rich repeat neuronal 3 [Source:HGNC Symbol;Acc:HGNC:17200]"}, {"versioned_ensembl_gene_id":"ENSG00000230178.1","gene_symbol":"OR4F3","gene_name":"olfactory receptor family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:8300]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26683","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":181367268,"end":181368262,"strand":1,"description":"olfactory receptor family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:8300]"}, {"versioned_ensembl_gene_id":"ENSG00000241723.1","gene_symbol":"AC074276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158275809,"end":158276421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197771.12","gene_symbol":"MCMBP","gene_name":"minichromosome maintenance complex binding protein [Source:HGNC Symbol;Acc:HGNC:25782]","synonyms":"C10orf119,MCM-BP,FLJ13081","biotype":"protein_coding","ncbi_id":"79892","summary":"This gene encodes a protein which is a component of the hexameric minichromosome maintenance (MCM) complex which regulates initiation and elongation of DNA. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":119829404,"end":119892556,"strand":-1,"description":"minichromosome maintenance complex binding protein [Source:HGNC Symbol;Acc:HGNC:25782]"}, {"versioned_ensembl_gene_id":"ENSG00000093134.14","gene_symbol":"VNN3","gene_name":"vanin 3 [Source:HGNC Symbol;Acc:HGNC:16431]","synonyms":"HSA238982","biotype":"protein_coding","ncbi_id":"55350","summary":"This gene is the central gene in a cluster of three vanin genes on chromosome 6q23-q24. Extensive alternative splicing has been described; the two most common variants are represented as RefSeqs. [provided by RefSeq, Apr 2014]","start":132722787,"end":132734765,"strand":-1,"description":"vanin 3 [Source:HGNC Symbol;Acc:HGNC:16431]"}, {"versioned_ensembl_gene_id":"ENSG00000251291.1","gene_symbol":"LINC02462","gene_name":"long intergenic non-protein coding RNA 2462 [Source:HGNC Symbol;Acc:HGNC:53399]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377434","summary":null,"start":134423867,"end":134457852,"strand":1,"description":"long intergenic non-protein coding RNA 2462 [Source:HGNC Symbol;Acc:HGNC:53399]"}, {"versioned_ensembl_gene_id":"ENSG00000226571.1","gene_symbol":"AL158850.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139271362,"end":139287307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228614.1","gene_symbol":"AL513211.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53790875,"end":53794274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211819.3","gene_symbol":"TRAV40","gene_name":"T-cell receptor alpha variable 40 [Source:HGNC Symbol;Acc:HGNC:12141]","synonyms":"TCRAV40S1,TCRAV31S1","biotype":"TR_V_gene","ncbi_id":"28641","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22314490,"end":22314919,"strand":1,"description":"T-cell receptor alpha variable 40 [Source:HGNC Symbol;Acc:HGNC:12141]"}, {"versioned_ensembl_gene_id":"ENSG00000180872.4","gene_symbol":"DEFB112","gene_name":"defensin beta 112 [Source:HGNC Symbol;Acc:HGNC:18093]","synonyms":"DEFB-12","biotype":"protein_coding","ncbi_id":"245915","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":50043575,"end":50048651,"strand":-1,"description":"defensin beta 112 [Source:HGNC Symbol;Acc:HGNC:18093]"}, {"versioned_ensembl_gene_id":"ENSG00000163376.11","gene_symbol":"KBTBD8","gene_name":"kelch repeat and BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:30691]","synonyms":"TA-KRP,KIAA1842","biotype":"protein_coding","ncbi_id":"84541","summary":null,"start":66998307,"end":67011210,"strand":1,"description":"kelch repeat and BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:30691]"}, {"versioned_ensembl_gene_id":"ENSG00000270300.2","gene_symbol":"PHACTR2P1","gene_name":"phosphatase and actin regulator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49488]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100533676","summary":null,"start":119793589,"end":119816642,"strand":-1,"description":"phosphatase and actin regulator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49488]"}, {"versioned_ensembl_gene_id":"ENSG00000280381.1","gene_symbol":"AC026362.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123087256,"end":123092821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248401.2","gene_symbol":"AC114781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83247179,"end":83248206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238273.3","gene_symbol":"AC108058.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105363038,"end":105378839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235491.1","gene_symbol":"LINC01889","gene_name":"long intergenic non-protein coding RNA 1889 [Source:HGNC Symbol;Acc:HGNC:52708]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373597","summary":null,"start":125710969,"end":125765842,"strand":1,"description":"long intergenic non-protein coding RNA 1889 [Source:HGNC Symbol;Acc:HGNC:52708]"}, {"versioned_ensembl_gene_id":"ENSG00000280402.1","gene_symbol":"AC093525.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2578395,"end":2579963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226965.1","gene_symbol":"AC092167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110432239,"end":110534754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278330.1","gene_symbol":"AC018529.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77112602,"end":77115726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278424.1","gene_symbol":"AC073114.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110215891,"end":110216380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232199.1","gene_symbol":"RPL3P8","gene_name":"ribosomal protein L3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646620","summary":null,"start":109998434,"end":109999624,"strand":-1,"description":"ribosomal protein L3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35498]"}, {"versioned_ensembl_gene_id":"ENSG00000251661.3","gene_symbol":"AC136475.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":318640,"end":325631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281787.1","gene_symbol":"AF250324.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189790922,"end":189906229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204356.13","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"RDP,NELF-E,RDBP,D6S45,RD","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31952087,"end":31959110,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000109111.14","gene_symbol":"SUPT6H","gene_name":"SPT6 homolog, histone chaperone [Source:HGNC Symbol;Acc:HGNC:11470]","synonyms":"SPT6H,KIAA0162","biotype":"protein_coding","ncbi_id":"6830","summary":null,"start":28662091,"end":28702684,"strand":1,"description":"SPT6 homolog, histone chaperone [Source:HGNC Symbol;Acc:HGNC:11470]"}, {"versioned_ensembl_gene_id":"ENSG00000282675.1","gene_symbol":"AC245078.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11155045,"end":11155955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240827.1","gene_symbol":"AC021660.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98620065,"end":98620618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203685.9","gene_symbol":"STUM","gene_name":"stum, mechanosensory transduction mediator homolog [Source:HGNC Symbol;Acc:HGNC:30491]","synonyms":"DKFZp761P211,C1orf95","biotype":"protein_coding","ncbi_id":"375057","summary":null,"start":226548800,"end":226609214,"strand":1,"description":"stum, mechanosensory transduction mediator homolog [Source:HGNC Symbol;Acc:HGNC:30491]"}, {"versioned_ensembl_gene_id":"ENSG00000106927.11","gene_symbol":"AMBP","gene_name":"alpha-1-microglobulin/bikunin precursor [Source:HGNC Symbol;Acc:HGNC:453]","synonyms":"UTI,ITILC,ITIL,ITI,IATIL,HI30,HCP,EDC1","biotype":"protein_coding","ncbi_id":"259","summary":"This gene encodes a complex glycoprotein secreted in plasma. The precursor is proteolytically processed into distinct functioning proteins: alpha-1-microglobulin, which belongs to the superfamily of lipocalin transport proteins and may play a role in the regulation of inflammatory processes, and bikunin, which is a urinary trypsin inhibitor belonging to the superfamily of Kunitz-type protease inhibitors and plays an important role in many physiological and pathological processes. This gene is located on chromosome 9 in a cluster of lipocalin genes. [provided by RefSeq, Jul 2008]","start":114060127,"end":114078472,"strand":-1,"description":"alpha-1-microglobulin/bikunin precursor [Source:HGNC Symbol;Acc:HGNC:453]"}, {"versioned_ensembl_gene_id":"ENSG00000138336.8","gene_symbol":"TET1","gene_name":"tet methylcytosine dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:29484]","synonyms":"LCX,KIAA1676,CXXC6,bA119F7.1","biotype":"protein_coding","ncbi_id":"80312","summary":"DNA methylation is an epigenetic mechanism that is important for controlling gene expression. The protein encoded by this gene is a demethylase that belongs to the TET (ten-eleven translocation) family. Members of the TET protein family play a role in the DNA methylation process and gene activation. [provided by RefSeq, Sep 2015]","start":68560656,"end":68694482,"strand":1,"description":"tet methylcytosine dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:29484]"}, {"versioned_ensembl_gene_id":"ENSG00000105698.15","gene_symbol":"USF2","gene_name":"upstream transcription factor 2, c-fos interacting [Source:HGNC Symbol;Acc:HGNC:12594]","synonyms":"FIP,bHLHb12","biotype":"protein_coding","ncbi_id":"7392","summary":"This gene encodes a member of the basic helix-loop-helix leucine zipper family of transcription factors. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs and is involved in regulating multiple cellular processes. [provided by RefSeq, Mar 2016]","start":35268978,"end":35279821,"strand":1,"description":"upstream transcription factor 2, c-fos interacting [Source:HGNC Symbol;Acc:HGNC:12594]"}, {"versioned_ensembl_gene_id":"ENSG00000105492.15","gene_symbol":"SIGLEC6","gene_name":"sialic acid binding Ig like lectin 6 [Source:HGNC Symbol;Acc:HGNC:10875]","synonyms":"SIGLEC-6,OB-BP1,CD33L1,CD33L,CD327","biotype":"protein_coding","ncbi_id":"946","summary":"This gene encodes a member of the SIGLEC (sialic acid binding immunoglobulin-like lectin) family of proteins. The encoded transmembrane receptor binds sialyl-TN glycans and leptin. Placental expression of the encoded protein is upregulated in preeclampsia. [provided by RefSeq, Jul 2016]","start":51519525,"end":51531856,"strand":-1,"description":"sialic acid binding Ig like lectin 6 [Source:HGNC Symbol;Acc:HGNC:10875]"}, {"versioned_ensembl_gene_id":"ENSG00000244470.2","gene_symbol":"AC105918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104886118,"end":104886955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185614.4","gene_symbol":"FAM212A","gene_name":"family with sequence similarity 212 member A [Source:HGNC Symbol;Acc:HGNC:32480]","synonyms":"INKA1,C3orf54","biotype":"protein_coding","ncbi_id":"389119","summary":null,"start":49803254,"end":49805030,"strand":1,"description":"family with sequence similarity 212 member A [Source:HGNC Symbol;Acc:HGNC:32480]"}, {"versioned_ensembl_gene_id":"ENSG00000269405.6","gene_symbol":"NXF2","gene_name":"nuclear RNA export factor 2 [Source:HGNC Symbol;Acc:HGNC:8072]","synonyms":"TAPL-2,CT39","biotype":"protein_coding","ncbi_id":"56001","summary":"This gene encodes a member of a family of nuclear RNA export proteins. The encoded protein is associated with the nuclear envelope and aids in the export of mRNAs. There is a closely related paralog of this gene located adjacent on chromosome X and on the opposite strand. [provided by RefSeq, Aug 2013]","start":102247161,"end":102326719,"strand":1,"description":"nuclear RNA export factor 2 [Source:HGNC Symbol;Acc:HGNC:8072]"}, {"versioned_ensembl_gene_id":"ENSG00000273746.1","gene_symbol":"AC234791.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102259043,"end":102261692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136160.14","gene_symbol":"EDNRB","gene_name":"endothelin receptor type B [Source:HGNC Symbol;Acc:HGNC:3180]","synonyms":"HSCR2,HSCR,ETB","biotype":"protein_coding","ncbi_id":"1910","summary":"The protein encoded by this gene is a G protein-coupled receptor which activates a phosphatidylinositol-calcium second messenger system. Its ligand, endothelin, consists of a family of three potent vasoactive peptides: ET1, ET2, and ET3. Studies suggest that the multigenic disorder, Hirschsprung disease type 2, is due to mutations in the endothelin receptor type B gene. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":77895481,"end":77919768,"strand":-1,"description":"endothelin receptor type B [Source:HGNC Symbol;Acc:HGNC:3180]"}, {"versioned_ensembl_gene_id":"ENSG00000226148.1","gene_symbol":"SLC25A39P1","gene_name":"solute carrier family 25 member 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43859]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420877","summary":null,"start":202796030,"end":202797094,"strand":1,"description":"solute carrier family 25 member 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43859]"}, {"versioned_ensembl_gene_id":"ENSG00000249614.1","gene_symbol":"LINC02503","gene_name":"long intergenic non-protein coding RNA 2503 [Source:HGNC Symbol;Acc:HGNC:53492]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377349","summary":null,"start":103961616,"end":104036923,"strand":1,"description":"long intergenic non-protein coding RNA 2503 [Source:HGNC Symbol;Acc:HGNC:53492]"}, {"versioned_ensembl_gene_id":"ENSG00000271723.5","gene_symbol":"MROH7-TTC4","gene_name":"MROH7-TTC4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527960","summary":"This locus represents naturally occurring read-through transcription between the neighboring MROH7 (maestro heat-like repeat family member 7) and TTC4 (tetratricopeptide repeat domain 4) genes. Alternative splicing results in multiple transcript variants, which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to produce protein products. [provided by RefSeq, Aug 2013]","start":54641786,"end":54742308,"strand":1,"description":"MROH7-TTC4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49180]"}, {"versioned_ensembl_gene_id":"ENSG00000147274.14","gene_symbol":"RBMX","gene_name":"RNA binding motif protein, X-linked [Source:HGNC Symbol;Acc:HGNC:9910]","synonyms":"RNMX,HNRNPG,hnRNP-G","biotype":"protein_coding","ncbi_id":"27316","summary":"This gene belongs to the RBMY gene family which includes candidate Y chromosome spermatogenesis genes. This gene, an active X chromosome homolog of the Y chromosome RBMY gene, is widely expressed whereas the RBMY gene evolved a male-specific function in spermatogenesis. Pseudogenes of this gene, found on chromosomes 1, 4, 9, 11, and 6, were likely derived by retrotransposition from the original gene. Alternatively spliced transcript variants encoding different isoforms have been identified. A snoRNA gene (SNORD61) is found in one of its introns. [provided by RefSeq, Sep 2009]","start":136848004,"end":136880764,"strand":-1,"description":"RNA binding motif protein, X-linked [Source:HGNC Symbol;Acc:HGNC:9910]"}, {"versioned_ensembl_gene_id":"ENSG00000221093.1","gene_symbol":"SNORA3","gene_name":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56121242,"end":56121352,"strand":-1,"description":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]"}, {"versioned_ensembl_gene_id":"ENSG00000104522.15","gene_symbol":"TSTA3","gene_name":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]","synonyms":"SDR4E1,P35B,FX","biotype":"protein_coding","ncbi_id":"7264","summary":"Tissue specific transplantation antigen P35B is a NADP(H)-binding protein. It catalyze the two-step epimerase and the reductase reactions in GDP-D-mannose metabolism, converting GDP-4-keto-6-D-deoxymannose to GDP-L-fucose. GDP-L-fucose is the substrate of several fucosyltransferases involved in the expression of many glycoconjugates, including blood group ABH antigens and developmental adhesion antigens. Mutations in this gene may cause leukocyte adhesion deficiency, type II. [provided by RefSeq, Jul 2008]","start":143612618,"end":143618048,"strand":-1,"description":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]"}, {"versioned_ensembl_gene_id":"ENSG00000139668.8","gene_symbol":"WDFY2","gene_name":"WD repeat and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20482]","synonyms":"ZFYVE22","biotype":"protein_coding","ncbi_id":"115825","summary":"This gene encodes a protein that contains two WD domains and an FYVE zinc finger region. The function of this gene is unknown. An alternatively spliced transcript variant of this gene may exist. [provided by RefSeq, Jul 2008]","start":51584455,"end":51767707,"strand":1,"description":"WD repeat and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20482]"}, {"versioned_ensembl_gene_id":"ENSG00000228577.1","gene_symbol":"AC010731.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206606497,"end":206609812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196388.8","gene_symbol":"INCA1","gene_name":"inhibitor of CDK, cyclin A1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:32224]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388324","summary":null,"start":4988130,"end":4997610,"strand":-1,"description":"inhibitor of CDK, cyclin A1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:32224]"}, {"versioned_ensembl_gene_id":"ENSG00000181392.14","gene_symbol":"SYNE4","gene_name":"spectrin repeat containing nuclear envelope family member 4 [Source:HGNC Symbol;Acc:HGNC:26703]","synonyms":"Nesprin-4,Nesp4,FLJ36445,DFNB76,C19orf46","biotype":"protein_coding","ncbi_id":"163183","summary":"This gene is a member of the nesprin family of genes, that encode KASH (Klarsicht, Anc-1, Syne Homology) domain-containing proteins. In addition to the KASH domain, this protein also contains a coiled-coil and leucine zipper region, a spectrin repeat, and a kinesin-1 binding region. This protein localizes to the outer nuclear membrane, and is part of the linker of nucleoskeleton and cytoskeleton (LINC) complex in the nuclear envelope. LINC complexes are formed by SUN (Sad1, UNC-84)-KASH pairs, and are thought to mechanically couple nuclear components to the cytoskeleton. Mutations in this gene have been associated with progressive high-frequency hearing loss. The absence of this protein in mice also caused hearing loss, and changes in hair cell morphology in the ears. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":36003307,"end":36008793,"strand":-1,"description":"spectrin repeat containing nuclear envelope family member 4 [Source:HGNC Symbol;Acc:HGNC:26703]"}, {"versioned_ensembl_gene_id":"ENSG00000168062.9","gene_symbol":"BATF2","gene_name":"basic leucine zipper ATF-like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:25163]","synonyms":"MGC20410","biotype":"protein_coding","ncbi_id":"116071","summary":null,"start":64987943,"end":64997045,"strand":-1,"description":"basic leucine zipper ATF-like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:25163]"}, {"versioned_ensembl_gene_id":"ENSG00000270647.5","gene_symbol":"TAF15","gene_name":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]","synonyms":"TAF2N,RBP56,Npl3,hTAFII68","biotype":"protein_coding","ncbi_id":"8148","summary":"This gene encodes a member of the TET family of RNA-binding proteins. The encoded protein plays a role in RNA polymerase II gene transcription as a component of a distinct subset of multi-subunit transcription initiation factor TFIID complexes. Translocations involving this gene play a role in acute leukemia and extraskeletal myxoid chondrosarcoma, and mutations in this gene may play a role in amyotrophic lateral sclerosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":35713791,"end":35864615,"strand":1,"description":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]"}, {"versioned_ensembl_gene_id":"ENSG00000276294.1","gene_symbol":"AC078899.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20330121,"end":20331517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271638.1","gene_symbol":"BNIP3P19","gene_name":"BCL2 interacting protein 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480281","summary":null,"start":20323992,"end":20324568,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49699]"}, {"versioned_ensembl_gene_id":"ENSG00000271583.1","gene_symbol":"AC103881.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146833501,"end":146834038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233246.1","gene_symbol":"AL513327.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33350352,"end":33363245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198526.7","gene_symbol":"PABPC1P2","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8559]","synonyms":"PABP4,PABP2,PABPCP4,PABPCP2","biotype":"processed_pseudogene","ncbi_id":"728773","summary":null,"start":146587506,"end":146589310,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8559]"}, {"versioned_ensembl_gene_id":"ENSG00000223459.5","gene_symbol":"TCAF1P1","gene_name":"TRPM8 channel associated factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33604]","synonyms":"FAM115B","biotype":"unprocessed_pseudogene","ncbi_id":"653199","summary":null,"start":143598040,"end":143604839,"strand":1,"description":"TRPM8 channel associated factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33604]"}, {"versioned_ensembl_gene_id":"ENSG00000264019.1","gene_symbol":"AC018521.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47946802,"end":47948275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230162.1","gene_symbol":"CT45A11P","gene_name":"cancer/testis antigen family 45 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:51336]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129813","summary":null,"start":135942478,"end":135947139,"strand":-1,"description":"cancer/testis antigen family 45 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:51336]"}, {"versioned_ensembl_gene_id":"ENSG00000167183.2","gene_symbol":"PRR15L","gene_name":"proline rich 15 like [Source:HGNC Symbol;Acc:HGNC:28149]","synonyms":"ATAD4,MGC11242","biotype":"protein_coding","ncbi_id":"79170","summary":null,"start":47951967,"end":47957878,"strand":-1,"description":"proline rich 15 like [Source:HGNC Symbol;Acc:HGNC:28149]"}, {"versioned_ensembl_gene_id":"ENSG00000136897.7","gene_symbol":"MRPL50","gene_name":"mitochondrial ribosomal protein L50 [Source:HGNC Symbol;Acc:HGNC:16654]","synonyms":"MRP-L50,FLJ20493","biotype":"protein_coding","ncbi_id":"54534","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a putative 39S subunit protein and belongs to the L47P ribosomal protein family. Pseudogenes corresponding to this gene are found on chromosomes 2p, 2q, 5p, and 10q. [provided by RefSeq, Jul 2008]","start":101387633,"end":101398614,"strand":-1,"description":"mitochondrial ribosomal protein L50 [Source:HGNC Symbol;Acc:HGNC:16654]"}, {"versioned_ensembl_gene_id":"ENSG00000185701.7","gene_symbol":"OR5M5P","gene_name":"olfactory receptor family 5 subfamily M member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14810]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390166","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56526568,"end":56527503,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14810]"}, {"versioned_ensembl_gene_id":"ENSG00000271366.1","gene_symbol":"AC002128.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35251440,"end":35253639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272915.1","gene_symbol":"AC018635.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128264526,"end":128264889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255790.5","gene_symbol":"AC078950.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11399381,"end":11486678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181371.4","gene_symbol":"OR5M8","gene_name":"olfactory receptor family 5 subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:14846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219484","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56490349,"end":56491395,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:14846]"}, {"versioned_ensembl_gene_id":"ENSG00000235357.1","gene_symbol":"LINC01621","gene_name":"long intergenic non-protein coding RNA 1621 [Source:HGNC Symbol;Acc:HGNC:14109]","synonyms":"C6orf7","biotype":"lincRNA","ncbi_id":"89758","summary":null,"start":79803583,"end":79807225,"strand":-1,"description":"long intergenic non-protein coding RNA 1621 [Source:HGNC Symbol;Acc:HGNC:14109]"}, {"versioned_ensembl_gene_id":"ENSG00000091483.6","gene_symbol":"FH","gene_name":"fumarate hydratase [Source:HGNC Symbol;Acc:HGNC:3700]","synonyms":"fumarase","biotype":"protein_coding","ncbi_id":"2271","summary":"The protein encoded by this gene is an enzymatic component of the tricarboxylic acid (TCA) cycle, or Krebs cycle, and catalyzes the formation of L-malate from fumarate. It exists in both a cytosolic form and an N-terminal extended form, differing only in the translation start site used. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension generates the same form as in the cytoplasm. It is similar to some thermostable class II fumarases and functions as a homotetramer. Mutations in this gene can cause fumarase deficiency and lead to progressive encephalopathy. [provided by RefSeq, Jul 2008]","start":241497603,"end":241519761,"strand":-1,"description":"fumarate hydratase [Source:HGNC Symbol;Acc:HGNC:3700]"}, {"versioned_ensembl_gene_id":"ENSG00000258625.2","gene_symbol":"OR11H5P","gene_name":"olfactory receptor family 11 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15348]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390440","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20204606,"end":20210498,"strand":1,"description":"olfactory receptor family 11 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15348]"}, {"versioned_ensembl_gene_id":"ENSG00000180828.2","gene_symbol":"BHLHE22","gene_name":"basic helix-loop-helix family member e22 [Source:HGNC Symbol;Acc:HGNC:11963]","synonyms":"BHLHB5,Beta3,TNRC20,CAGL85,bHLHe22","biotype":"protein_coding","ncbi_id":"27319","summary":"This gene encodes a protein that belongs to the basic helix-loop-helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis. [provided by RefSeq, Oct 2016]","start":64580367,"end":64583628,"strand":1,"description":"basic helix-loop-helix family member e22 [Source:HGNC Symbol;Acc:HGNC:11963]"}, {"versioned_ensembl_gene_id":"ENSG00000243729.4","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29353749,"end":29431967,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000234347.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425439,"end":29457001,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000255441.1","gene_symbol":"AC008750.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51415724,"end":51417425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233206.1","gene_symbol":"RPS3AP1","gene_name":"ribosomal protein S3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10422]","synonyms":"RPS3AP","biotype":"processed_pseudogene","ncbi_id":"101241875","summary":null,"start":20430443,"end":20430762,"strand":-1,"description":"ribosomal protein S3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10422]"}, {"versioned_ensembl_gene_id":"ENSG00000206280.7","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"fru,ZNF297,BING1,ZBTB22A,fruitless,ZNF297A","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33243252,"end":33246776,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000262366.1","gene_symbol":"NDUFA3P6","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479052","summary":null,"start":31174573,"end":31174822,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45055]"}, {"versioned_ensembl_gene_id":"ENSG00000234439.1","gene_symbol":"KRT18P2","gene_name":"keratin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6435]","synonyms":"OTTHUMG00000078062","biotype":"processed_pseudogene","ncbi_id":"54044","summary":null,"start":20424949,"end":20426206,"strand":-1,"description":"keratin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6435]"}, {"versioned_ensembl_gene_id":"ENSG00000233676.2","gene_symbol":"FDPSP6","gene_name":"farnesyl diphosphate synthase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3637]","synonyms":"FDPSP","biotype":"processed_pseudogene","ncbi_id":"54051","summary":null,"start":20388334,"end":20388845,"strand":1,"description":"farnesyl diphosphate synthase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3637]"}, {"versioned_ensembl_gene_id":"ENSG00000229953.1","gene_symbol":"AL590666.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156646507,"end":156661424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235482.1","gene_symbol":"RPL21P135","gene_name":"ribosomal protein L21 pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:44539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419391","summary":null,"start":37748110,"end":37748900,"strand":1,"description":"ribosomal protein L21 pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:44539]"}, {"versioned_ensembl_gene_id":"ENSG00000253737.1","gene_symbol":"AP003469.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101139665,"end":101140929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226856.5","gene_symbol":"AC093901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118132128,"end":118186386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207112.1","gene_symbol":"SNORA25","gene_name":"small nucleolar RNA, H/ACA box 25 [Source:HGNC Symbol;Acc:HGNC:32615]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":93730513,"end":93730646,"strand":-1,"description":"small nucleolar RNA, H/ACA box 25 [Source:HGNC Symbol;Acc:HGNC:32615]"}, {"versioned_ensembl_gene_id":"ENSG00000223448.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31620003,"end":31621970,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000231584.8","gene_symbol":"FAHD2CP","gene_name":"fumarylacetoacetate hydrolase domain containing 2C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44135]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729234","summary":null,"start":96010551,"end":96023380,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 2C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44135]"}, {"versioned_ensembl_gene_id":"ENSG00000224233.1","gene_symbol":"AL645937.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181510,"end":29182445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065183.15","gene_symbol":"WDR3","gene_name":"WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12755]","synonyms":"UTP12,FLJ12796,DIP2","biotype":"protein_coding","ncbi_id":"10885","summary":"This gene encodes a nuclear protein containing 10 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, which usually include a trp-asp at the C-terminal end. Proteins belonging to the WD repeat family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]","start":117929720,"end":117966542,"strand":1,"description":"WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12755]"}, {"versioned_ensembl_gene_id":"ENSG00000185873.7","gene_symbol":"TMPRSS11B","gene_name":"transmembrane protease, serine 11B [Source:HGNC Symbol;Acc:HGNC:25398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132724","summary":null,"start":68226653,"end":68245720,"strand":-1,"description":"transmembrane protease, serine 11B [Source:HGNC Symbol;Acc:HGNC:25398]"}, {"versioned_ensembl_gene_id":"ENSG00000205718.9","gene_symbol":"MBD3L4","gene_name":"methyl-CpG binding domain protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:37206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653656","summary":"This gene encodes a member of a family of proteins that are related to methyl-CpG-binding proteins but lack the methyl-CpG binding domain. There is no definitive support for transcription of this locus, and the transcript structure is inferred from other family members. [provided by RefSeq, Aug 2009]","start":7037748,"end":7040179,"strand":-1,"description":"methyl-CpG binding domain protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:37206]"}, {"versioned_ensembl_gene_id":"ENSG00000260395.1","gene_symbol":"AC092119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21998310,"end":21999656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273040.1","gene_symbol":"BX908720.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837838,"end":28838975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241880.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29720644,"end":29721114,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000270610.1","gene_symbol":"AL160191.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70234495,"end":70235095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182365.4","gene_symbol":"OR5F2P","gene_name":"olfactory receptor family 5 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15286]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56015017,"end":56015957,"strand":-1,"description":"olfactory receptor family 5 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15286]"}, {"versioned_ensembl_gene_id":"ENSG00000251686.1","gene_symbol":"OR10J8P","gene_name":"olfactory receptor family 10 subfamily J member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:19638]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"343409","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159366161,"end":159367089,"strand":1,"description":"olfactory receptor family 10 subfamily J member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:19638]"}, {"versioned_ensembl_gene_id":"ENSG00000167965.17","gene_symbol":"MLST8","gene_name":"MTOR associated protein, LST8 homolog [Source:HGNC Symbol;Acc:HGNC:24825]","synonyms":"Pop3,Lst8,GBL,GbetaL","biotype":"protein_coding","ncbi_id":"64223","summary":null,"start":2204248,"end":2209416,"strand":1,"description":"MTOR associated protein, LST8 homolog [Source:HGNC Symbol;Acc:HGNC:24825]"}, {"versioned_ensembl_gene_id":"ENSG00000258816.1","gene_symbol":"AC121758.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56855694,"end":56855886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231934.1","gene_symbol":"LINC01598","gene_name":"long intergenic non-protein coding RNA 1598 [Source:HGNC Symbol;Acc:HGNC:51597]","synonyms":"TCONS_00028363","biotype":"antisense_RNA","ncbi_id":"105379478","summary":null,"start":30323812,"end":30361730,"strand":-1,"description":"long intergenic non-protein coding RNA 1598 [Source:HGNC Symbol;Acc:HGNC:51597]"}, {"versioned_ensembl_gene_id":"ENSG00000255273.1","gene_symbol":"AF238378.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7082971,"end":7083328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253321.1","gene_symbol":"AC099554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90353037,"end":90356609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204555.3","gene_symbol":"CFTRP3","gene_name":"cystic fibrosis transmembrane conductance regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481718","summary":null,"start":30214765,"end":30214976,"strand":-1,"description":"cystic fibrosis transmembrane conductance regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51352]"}, {"versioned_ensembl_gene_id":"ENSG00000227206.1","gene_symbol":"AL645937.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29124210,"end":29128908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197587.10","gene_symbol":"DMBX1","gene_name":"diencephalon/mesencephalon homeobox 1 [Source:HGNC Symbol;Acc:HGNC:19026]","synonyms":"PAXB,OTX3","biotype":"protein_coding","ncbi_id":"127343","summary":"This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":46506996,"end":46514226,"strand":1,"description":"diencephalon/mesencephalon homeobox 1 [Source:HGNC Symbol;Acc:HGNC:19026]"}, {"versioned_ensembl_gene_id":"ENSG00000100678.18","gene_symbol":"SLC8A3","gene_name":"solute carrier family 8 member A3 [Source:HGNC Symbol;Acc:HGNC:11070]","synonyms":"NCX3","biotype":"protein_coding","ncbi_id":"6547","summary":"This gene encodes a member of the sodium/calcium exchanger integral membrane protein family. Na+/Ca2+ exchange proteins are involved in maintaining Ca2+ homeostasis in a wide variety of cell types. The protein is regulated by intracellular calcium ions and is found in both the plasma membrane and intracellular organellar membranes, where exchange of Na+ for Ca2+ occurs in an electrogenic manner. Alternative splicing has been observed for this gene and multiple variants have been described. [provided by RefSeq, Aug 2013]","start":70044217,"end":70189070,"strand":-1,"description":"solute carrier family 8 member A3 [Source:HGNC Symbol;Acc:HGNC:11070]"}, {"versioned_ensembl_gene_id":"ENSG00000250756.1","gene_symbol":"AC018645.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32788334,"end":32788442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142910.15","gene_symbol":"TINAGL1","gene_name":"tubulointerstitial nephritis antigen like 1 [Source:HGNC Symbol;Acc:HGNC:19168]","synonyms":"TINAGRP,P3ECSL,LIECG3,LCN7,ARG1","biotype":"protein_coding","ncbi_id":"64129","summary":"The protein encoded by this gene is similar in sequence to tubulointerstitial nephritis antigen, a secreted glycoprotein that is recognized by antibodies in some types of immune-related tubulointerstitial nephritis. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":31576485,"end":31587686,"strand":1,"description":"tubulointerstitial nephritis antigen like 1 [Source:HGNC Symbol;Acc:HGNC:19168]"}, {"versioned_ensembl_gene_id":"ENSG00000274110.4","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54283996,"end":54300924,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000136144.11","gene_symbol":"RCBTB1","gene_name":"RCC1 and BTB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:18243]","synonyms":"FLJ10716,CLLL7,CLLD7","biotype":"protein_coding","ncbi_id":"55213","summary":"This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies. [provided by RefSeq, Jul 2008]","start":49531946,"end":49585583,"strand":-1,"description":"RCC1 and BTB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:18243]"}, {"versioned_ensembl_gene_id":"ENSG00000198225.5","gene_symbol":"FKBP1C","gene_name":"FK506 binding protein 1C [Source:HGNC Symbol;Acc:HGNC:21376]","synonyms":"bA184C23.2","biotype":"protein_coding","ncbi_id":"642489","summary":null,"start":63211446,"end":63213024,"strand":1,"description":"FK506 binding protein 1C [Source:HGNC Symbol;Acc:HGNC:21376]"}, {"versioned_ensembl_gene_id":"ENSG00000269069.1","gene_symbol":"AC007842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40023384,"end":40025502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204702.5","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"polymorphic_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29099657,"end":29102701,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000136531.15","gene_symbol":"SCN2A","gene_name":"sodium voltage-gated channel alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:10588]","synonyms":"SCN2A2,SCN2A1,Nav1.2,HBSCII,HBSCI","biotype":"protein_coding","ncbi_id":"6326","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with four repeat domains, each of which is composed of six membrane-spanning segments, and one or more regulatory beta subunits. Voltage-gated sodium channels function in the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. Allelic variants of this gene are associated with seizure disorders and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":165194993,"end":165392310,"strand":1,"description":"sodium voltage-gated channel alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:10588]"}, {"versioned_ensembl_gene_id":"ENSG00000282911.1","gene_symbol":"ABBA01031663.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29448517,"end":29449306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171853.15","gene_symbol":"TRAPPC12","gene_name":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]","synonyms":"TTC15,TTC-15,CGI-87","biotype":"protein_coding","ncbi_id":"51112","summary":null,"start":3379675,"end":3485094,"strand":1,"description":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]"}, {"versioned_ensembl_gene_id":"ENSG00000032742.17","gene_symbol":"IFT88","gene_name":"intraflagellar transport 88 [Source:HGNC Symbol;Acc:HGNC:20606]","synonyms":"TTC10,Tg737,MGC26259,hTg737,D13S1056E","biotype":"protein_coding","ncbi_id":"8100","summary":"This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2017]","start":20567069,"end":20691437,"strand":1,"description":"intraflagellar transport 88 [Source:HGNC Symbol;Acc:HGNC:20606]"}, {"versioned_ensembl_gene_id":"ENSG00000183648.9","gene_symbol":"NDUFB1","gene_name":"NADH:ubiquinone oxidoreductase subunit B1 [Source:HGNC Symbol;Acc:HGNC:7695]","synonyms":"MNLL,CI-MNLL","biotype":"protein_coding","ncbi_id":"4707","summary":null,"start":92116122,"end":92121917,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B1 [Source:HGNC Symbol;Acc:HGNC:7695]"}, {"versioned_ensembl_gene_id":"ENSG00000171100.14","gene_symbol":"MTM1","gene_name":"myotubularin 1 [Source:HGNC Symbol;Acc:HGNC:7448]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4534","summary":"This gene encodes a dual-specificity phosphatase that acts on both phosphotyrosine and phosphoserine. It is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy. [provided by RefSeq, Jul 2008]","start":150568619,"end":150673322,"strand":1,"description":"myotubularin 1 [Source:HGNC Symbol;Acc:HGNC:7448]"}, {"versioned_ensembl_gene_id":"ENSG00000256625.1","gene_symbol":"AC092747.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27121910,"end":27147664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256226.1","gene_symbol":"AC092747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27105151,"end":27161393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223963.2","gene_symbol":"THAP12P8","gene_name":"THAP domain containing 12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39572]","synonyms":"PRKRIRP8","biotype":"processed_pseudogene","ncbi_id":"645939","summary":null,"start":240769420,"end":240771534,"strand":-1,"description":"THAP domain containing 12 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39572]"}, {"versioned_ensembl_gene_id":"ENSG00000255183.1","gene_symbol":"AP000756.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87718354,"end":87719411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258719.1","gene_symbol":"AC009396.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78695321,"end":78698122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258662.1","gene_symbol":"AC022469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79246668,"end":79249023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228927.10","gene_symbol":"TSPY3","gene_name":"testis specific protein, Y-linked 3 [Source:HGNC Symbol;Acc:HGNC:33876]","synonyms":"CT78","biotype":"protein_coding","ncbi_id":"728137","summary":null,"start":9398421,"end":9401223,"strand":1,"description":"testis specific protein, Y-linked 3 [Source:HGNC Symbol;Acc:HGNC:33876]"}, {"versioned_ensembl_gene_id":"ENSG00000223694.1","gene_symbol":"ADH5P3","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22991]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131810","summary":null,"start":240170155,"end":240171291,"strand":1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22991]"}, {"versioned_ensembl_gene_id":"ENSG00000267412.1","gene_symbol":"AC092068.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2610155,"end":2611862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147912.12","gene_symbol":"FBXO10","gene_name":"F-box protein 10 [Source:HGNC Symbol;Acc:HGNC:13589]","synonyms":"FBX10","biotype":"protein_coding","ncbi_id":"26267","summary":"Members of the F-box protein family, such as FBXO10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":37510892,"end":37576349,"strand":-1,"description":"F-box protein 10 [Source:HGNC Symbol;Acc:HGNC:13589]"}, {"versioned_ensembl_gene_id":"ENSG00000269021.1","gene_symbol":"AC063977.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51280862,"end":51283022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242071.3","gene_symbol":"RPL7AP6","gene_name":"ribosomal protein L7a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326310","summary":null,"start":69885340,"end":69886140,"strand":-1,"description":"ribosomal protein L7a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19785]"}, {"versioned_ensembl_gene_id":"ENSG00000272411.1","gene_symbol":"AC116312.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148970340,"end":148970653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215127.6","gene_symbol":"SYT14P1","gene_name":"synaptotagmin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33429]","synonyms":"SYTDEP,SYT14L,CHR415SYT","biotype":"transcribed_processed_pseudogene","ncbi_id":"401135","summary":null,"start":68061822,"end":68063269,"strand":-1,"description":"synaptotagmin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33429]"}, {"versioned_ensembl_gene_id":"ENSG00000227730.2","gene_symbol":"MTND6P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39468]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480427","summary":null,"start":5091093,"end":5091604,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39468]"}, {"versioned_ensembl_gene_id":"ENSG00000213088.9","gene_symbol":"ACKR1","gene_name":"atypical chemokine receptor 1 (Duffy blood group) [Source:HGNC Symbol;Acc:HGNC:4035]","synonyms":"GPD,FY,Dfy,DARC,CD234,CCBP1","biotype":"protein_coding","ncbi_id":"2532","summary":"The protein encoded by this gene is a glycosylated membrane protein and a non-specific receptor for several chemokines. The encoded protein is the receptor for the human malarial parasites Plasmodium vivax and Plasmodium knowlesi. Polymorphisms in this gene are the basis of the Duffy blood group system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":159203307,"end":159206500,"strand":1,"description":"atypical chemokine receptor 1 (Duffy blood group) [Source:HGNC Symbol;Acc:HGNC:4035]"}, {"versioned_ensembl_gene_id":"ENSG00000206487.11","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30636534,"end":30642598,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000254566.1","gene_symbol":"AC087277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36321158,"end":36323440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226841.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31519466,"end":31520981,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000264301.1","gene_symbol":"LINC01444","gene_name":"long intergenic non-protein coding RNA 1444 [Source:HGNC Symbol;Acc:HGNC:50769]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927642","summary":null,"start":14969001,"end":14970468,"strand":-1,"description":"long intergenic non-protein coding RNA 1444 [Source:HGNC Symbol;Acc:HGNC:50769]"}, {"versioned_ensembl_gene_id":"ENSG00000264061.1","gene_symbol":"FGF7P1","gene_name":"fibroblast growth factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21455]","synonyms":"HsT283","biotype":"unprocessed_pseudogene","ncbi_id":"387559","summary":null,"start":14888709,"end":14890086,"strand":-1,"description":"fibroblast growth factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21455]"}, {"versioned_ensembl_gene_id":"ENSG00000226538.1","gene_symbol":"RPL35AP4","gene_name":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]","synonyms":"BPG294E21.7,OTTHUMG00000140156","biotype":"processed_pseudogene","ncbi_id":"100048922","summary":null,"start":33529535,"end":33529636,"strand":-1,"description":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]"}, {"versioned_ensembl_gene_id":"ENSG00000229396.1","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"processed_transcript","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33469139,"end":33469421,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000079313.13","gene_symbol":"REXO1","gene_name":"RNA exonuclease 1 homolog [Source:HGNC Symbol;Acc:HGNC:24616]","synonyms":"TCEB3BP1,KIAA1138,EloA-BP1","biotype":"protein_coding","ncbi_id":"57455","summary":null,"start":1815246,"end":1848463,"strand":-1,"description":"RNA exonuclease 1 homolog [Source:HGNC Symbol;Acc:HGNC:24616]"}, {"versioned_ensembl_gene_id":"ENSG00000230580.1","gene_symbol":"AC021016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":218354075,"end":218354572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136147.17","gene_symbol":"PHF11","gene_name":"PHD finger protein 11 [Source:HGNC Symbol;Acc:HGNC:17024]","synonyms":"NY-REN-34,IGER,BCAP","biotype":"protein_coding","ncbi_id":"51131","summary":"This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":49495610,"end":49528987,"strand":1,"description":"PHD finger protein 11 [Source:HGNC Symbol;Acc:HGNC:17024]"}, {"versioned_ensembl_gene_id":"ENSG00000225007.1","gene_symbol":"AC000067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19667023,"end":19667555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279919.1","gene_symbol":"AC068880.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19277284,"end":19277573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250571.6","gene_symbol":"GLI4","gene_name":"GLI family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:4320]","synonyms":"HKR4,ZNF928","biotype":"protein_coding","ncbi_id":"2738","summary":null,"start":143267433,"end":143276931,"strand":1,"description":"GLI family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:4320]"}, {"versioned_ensembl_gene_id":"ENSG00000225094.3","gene_symbol":"SETP20","gene_name":"SET pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42939]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389217","summary":null,"start":109553243,"end":109554094,"strand":-1,"description":"SET pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42939]"}, {"versioned_ensembl_gene_id":"ENSG00000077254.14","gene_symbol":"USP33","gene_name":"ubiquitin specific peptidase 33 [Source:HGNC Symbol;Acc:HGNC:20059]","synonyms":"VDU1,KIAA1097","biotype":"protein_coding","ncbi_id":"23032","summary":"This gene encodes a deubiquinating enzyme important in a variety of processes, including Slit-dependent cell migration and beta-2 adrenergic receptor signaling. The protein is negatively regulated through ubiquitination by von Hippel-Lindau tumor protein (VHL). Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]","start":77695987,"end":77759852,"strand":-1,"description":"ubiquitin specific peptidase 33 [Source:HGNC Symbol;Acc:HGNC:20059]"}, {"versioned_ensembl_gene_id":"ENSG00000261505.1","gene_symbol":"AL031714.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1317891,"end":1322845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250754.5","gene_symbol":"LINC02436","gene_name":"long intergenic non-protein coding RNA 2436 [Source:HGNC Symbol;Acc:HGNC:53368]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928877","summary":null,"start":185051896,"end":185107248,"strand":1,"description":"long intergenic non-protein coding RNA 2436 [Source:HGNC Symbol;Acc:HGNC:53368]"}, {"versioned_ensembl_gene_id":"ENSG00000244692.3","gene_symbol":"RN7SL724P","gene_name":"RNA, 7SL, cytoplasmic 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:46740]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479487","summary":null,"start":139609669,"end":139609939,"strand":-1,"description":"RNA, 7SL, cytoplasmic 724, pseudogene [Source:HGNC Symbol;Acc:HGNC:46740]"}, {"versioned_ensembl_gene_id":"ENSG00000241604.3","gene_symbol":"RN7SL340P","gene_name":"RNA, 7SL, cytoplasmic 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:46356]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481016","summary":null,"start":29233090,"end":29233385,"strand":-1,"description":"RNA, 7SL, cytoplasmic 340, pseudogene [Source:HGNC Symbol;Acc:HGNC:46356]"}, {"versioned_ensembl_gene_id":"ENSG00000170421.12","gene_symbol":"KRT8","gene_name":"keratin 8 [Source:HGNC Symbol;Acc:HGNC:6446]","synonyms":"KO,K8,K2C8,CYK8,CK8,CARD2","biotype":"protein_coding","ncbi_id":"3856","summary":"This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":52897187,"end":52949954,"strand":-1,"description":"keratin 8 [Source:HGNC Symbol;Acc:HGNC:6446]"}, {"versioned_ensembl_gene_id":"ENSG00000171307.18","gene_symbol":"ZDHHC16","gene_name":"zinc finger DHHC-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20714]","synonyms":"APH2","biotype":"protein_coding","ncbi_id":"84287","summary":null,"start":97446131,"end":97457370,"strand":1,"description":"zinc finger DHHC-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20714]"}, {"versioned_ensembl_gene_id":"ENSG00000254544.1","gene_symbol":"PCNAP4","gene_name":"proliferating cell nuclear antigen pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390102","summary":null,"start":19274540,"end":19275269,"strand":-1,"description":"proliferating cell nuclear antigen pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43737]"}, {"versioned_ensembl_gene_id":"ENSG00000268336.1","gene_symbol":"SIGLEC20P","gene_name":"sialic acid binding Ig like lectin 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:15609]","synonyms":"SIGLECP4","biotype":"unprocessed_pseudogene","ncbi_id":"114192","summary":null,"start":51184905,"end":51190809,"strand":1,"description":"sialic acid binding Ig like lectin 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:15609]"}, {"versioned_ensembl_gene_id":"ENSG00000132763.14","gene_symbol":"MMACHC","gene_name":"methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria [Source:HGNC Symbol;Acc:HGNC:24525]","synonyms":"DKFZP564I122,cblC","biotype":"protein_coding","ncbi_id":"25974","summary":"The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009]","start":45500053,"end":45513382,"strand":1,"description":"methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria [Source:HGNC Symbol;Acc:HGNC:24525]"}, {"versioned_ensembl_gene_id":"ENSG00000149256.15","gene_symbol":"TENM4","gene_name":"teneurin transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:29945]","synonyms":"Ten-M4,ODZ4,KIAA1302","biotype":"protein_coding","ncbi_id":"26011","summary":"The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5. [provided by RefSeq, Oct 2016]","start":78652831,"end":79440948,"strand":-1,"description":"teneurin transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:29945]"}, {"versioned_ensembl_gene_id":"ENSG00000254672.1","gene_symbol":"AL136146.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35967010,"end":35968676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171608.15","gene_symbol":"PIK3CD","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta [Source:HGNC Symbol;Acc:HGNC:8977]","synonyms":"p110D","biotype":"protein_coding","ncbi_id":"5293","summary":"Phosphoinositide 3-kinases (PI3Ks) phosphorylate inositol lipids and are involved in the immune response. The protein encoded by this gene is a class I PI3K found primarily in leukocytes. Like other class I PI3Ks (p110-alpha p110-beta, and p110-gamma), the encoded protein binds p85 adapter proteins and GTP-bound RAS. However, unlike the other class I PI3Ks, this protein phosphorylates itself, not p85 protein.[provided by RefSeq, Jul 2010]","start":9651732,"end":9729114,"strand":1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta [Source:HGNC Symbol;Acc:HGNC:8977]"}, {"versioned_ensembl_gene_id":"ENSG00000227509.1","gene_symbol":"LINC01839","gene_name":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]","synonyms":"EIF2B5-IT1","biotype":"lincRNA","ncbi_id":"105374251","summary":null,"start":184505113,"end":184508399,"strand":1,"description":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]"}, {"versioned_ensembl_gene_id":"ENSG00000239650.4","gene_symbol":"GUSBP4","gene_name":"glucuronidase, beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18220]","synonyms":"SMA3-L,GUSBL2,FLJ13549,C6orf216,SMAC3L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375513","summary":null,"start":57919784,"end":57930291,"strand":-1,"description":"glucuronidase, beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18220]"}, {"versioned_ensembl_gene_id":"ENSG00000135766.8","gene_symbol":"EGLN1","gene_name":"egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]","synonyms":"ZMYND6,SM-20,PHD2,HIFPH2,C1orf12","biotype":"protein_coding","ncbi_id":"54583","summary":"The protein encoded by this gene catalyzes the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins. HIF is a transcriptional complex that plays a central role in mammalian oxygen homeostasis. This protein functions as a cellular oxygen sensor, and under normal oxygen concentration, modification by prolyl hydroxylation is a key regulatory event that targets HIF subunits for proteasomal destruction via the von Hippel-Lindau ubiquitylation complex. Mutations in this gene are associated with erythrocytosis familial type 3 (ECYT3). [provided by RefSeq, Nov 2009]","start":231363751,"end":231425044,"strand":-1,"description":"egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]"}, {"versioned_ensembl_gene_id":"ENSG00000213032.3","gene_symbol":"NDUFA3P3","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644482","summary":null,"start":225964179,"end":225964428,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45052]"}, {"versioned_ensembl_gene_id":"ENSG00000282620.1","gene_symbol":"MAPT-IT1","gene_name":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100130148","summary":null,"start":45907408,"end":45910423,"strand":1,"description":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]"}, {"versioned_ensembl_gene_id":"ENSG00000143416.20","gene_symbol":"SELENBP1","gene_name":"selenium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10719]","synonyms":"LPSB,hSP56,hSBP","biotype":"protein_coding","ncbi_id":"8991","summary":"This gene encodes a member of the selenium-binding protein family. Selenium is an essential nutrient that exhibits potent anticarcinogenic properties, and deficiency of selenium may cause certain neurologic diseases. The effects of selenium in preventing cancer and neurologic diseases may be mediated by selenium-binding proteins, and decreased expression of this gene may be associated with several types of cancer. The encoded protein may play a selenium-dependent role in ubiquitination/deubiquitination-mediated protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]","start":151364302,"end":151372733,"strand":-1,"description":"selenium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10719]"}, {"versioned_ensembl_gene_id":"ENSG00000185942.11","gene_symbol":"NKAIN3","gene_name":"sodium/potassium transporting ATPase interacting 3 [Source:HGNC Symbol;Acc:HGNC:26829]","synonyms":"FLJ39630,FAM77D","biotype":"protein_coding","ncbi_id":"286183","summary":"NKAIN3 is a member of a family of mammalian proteins (see NKAIN1; MIM 612871) with similarity to Drosophila Nkain (Gorokhova et al., 2007 [PubMed 17606467]).[supplied by OMIM, Jun 2009]","start":62248591,"end":62999652,"strand":1,"description":"sodium/potassium transporting ATPase interacting 3 [Source:HGNC Symbol;Acc:HGNC:26829]"}, {"versioned_ensembl_gene_id":"ENSG00000233122.2","gene_symbol":"CTAGE7P","gene_name":"CTAGE family member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:25111]","synonyms":"MGC33437,CTAGEP,CTAGE7,bA500G10.2,rcCTAGE5","biotype":"processed_pseudogene","ncbi_id":"119437","summary":null,"start":130106046,"end":130108481,"strand":1,"description":"CTAGE family member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:25111]"}, {"versioned_ensembl_gene_id":"ENSG00000137266.14","gene_symbol":"SLC22A23","gene_name":"solute carrier family 22 member 23 [Source:HGNC Symbol;Acc:HGNC:21106]","synonyms":"FLJ22174,C6orf85","biotype":"protein_coding","ncbi_id":"63027","summary":"SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]","start":3268962,"end":3457022,"strand":-1,"description":"solute carrier family 22 member 23 [Source:HGNC Symbol;Acc:HGNC:21106]"}, {"versioned_ensembl_gene_id":"ENSG00000263501.1","gene_symbol":"AC005828.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63305262,"end":63313521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240015.2","gene_symbol":"AC084024.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38123274,"end":38124651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131470.14","gene_symbol":"PSMC3IP","gene_name":"PSMC3 interacting protein [Source:HGNC Symbol;Acc:HGNC:17928]","synonyms":"TBPIP,HUMGT198A,Hop2,GT198","biotype":"protein_coding","ncbi_id":"29893","summary":"This gene encodes a protein that functions in meiotic recombination. It is a subunit of the PSMC3IP/MND1 complex, which interacts with PSMC3/TBP1 to stimulate DMC1- and RAD51-mediated strand exchange during meiosis. The protein encoded by this gene can also co-activate ligand-driven transcription mediated by estrogen, androgen, glucocorticoid, progesterone, and thyroid nuclear receptors. Mutations in this gene cause XX female gonadal dysgenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":42572315,"end":42577831,"strand":-1,"description":"PSMC3 interacting protein [Source:HGNC Symbol;Acc:HGNC:17928]"}, {"versioned_ensembl_gene_id":"ENSG00000141622.13","gene_symbol":"RNF165","gene_name":"ring finger protein 165 [Source:HGNC Symbol;Acc:HGNC:31696]","synonyms":"RNF111L2,ARKL2","biotype":"protein_coding","ncbi_id":"494470","summary":"Encoded in regions involved in pericentric inversions in patients with bipolar affective disorder. [provided by RefSeq, Jul 2008]","start":46326809,"end":46463140,"strand":1,"description":"ring finger protein 165 [Source:HGNC Symbol;Acc:HGNC:31696]"}, {"versioned_ensembl_gene_id":"ENSG00000264907.1","gene_symbol":"PRELID3BP3","gene_name":"PRELI domain containing 3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49065]","synonyms":"SLMO2P3","biotype":"processed_pseudogene","ncbi_id":"100128712","summary":null,"start":62841101,"end":62841645,"strand":1,"description":"PRELI domain containing 3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49065]"}, {"versioned_ensembl_gene_id":"ENSG00000188807.12","gene_symbol":"TMEM201","gene_name":"transmembrane protein 201 [Source:HGNC Symbol;Acc:HGNC:33719]","synonyms":"SAMP1,RP13-15M17.2,NET5,Ima1","biotype":"protein_coding","ncbi_id":"199953","summary":null,"start":9588922,"end":9614873,"strand":1,"description":"transmembrane protein 201 [Source:HGNC Symbol;Acc:HGNC:33719]"}, {"versioned_ensembl_gene_id":"ENSG00000216412.4","gene_symbol":"RPL12P2","gene_name":"ribosomal protein L12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16070]","synonyms":"dJ441G21.1","biotype":"processed_pseudogene","ncbi_id":"646875","summary":null,"start":37091314,"end":37091806,"strand":1,"description":"ribosomal protein L12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16070]"}, {"versioned_ensembl_gene_id":"ENSG00000149091.15","gene_symbol":"DGKZ","gene_name":"diacylglycerol kinase zeta [Source:HGNC Symbol;Acc:HGNC:2857]","synonyms":"DGK-ZETA,DAGK6,DAGK5,hDGKzeta","biotype":"protein_coding","ncbi_id":"8525","summary":"The protein encoded by this gene belongs to the eukaryotic diacylglycerol kinase family. It may attenuate protein kinase C activity by regulating diacylglycerol levels in intracellular signaling cascade and signal transduction. Alternative splicing occurs at this locus and multiple transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Nov 2010]","start":46332905,"end":46380554,"strand":1,"description":"diacylglycerol kinase zeta [Source:HGNC Symbol;Acc:HGNC:2857]"}, {"versioned_ensembl_gene_id":"ENSG00000188818.12","gene_symbol":"ZDHHC11","gene_name":"zinc finger DHHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:19158]","synonyms":"ZNF399,FLJ13153","biotype":"protein_coding","ncbi_id":"79844","summary":null,"start":795606,"end":850986,"strand":-1,"description":"zinc finger DHHC-type containing 11 [Source:HGNC Symbol;Acc:HGNC:19158]"}, {"versioned_ensembl_gene_id":"ENSG00000237320.2","gene_symbol":"AC019064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34998273,"end":35000160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005238.19","gene_symbol":"FAM214B","gene_name":"family with sequence similarity 214 member B [Source:HGNC Symbol;Acc:HGNC:25666]","synonyms":"KIAA1539,FLJ11560,bA182N22.6","biotype":"protein_coding","ncbi_id":"80256","summary":null,"start":35104112,"end":35116341,"strand":-1,"description":"family with sequence similarity 214 member B [Source:HGNC Symbol;Acc:HGNC:25666]"}, {"versioned_ensembl_gene_id":"ENSG00000258913.1","gene_symbol":"C14orf144","gene_name":"chromosome 14 open reading frame 144 [Source:NCBI gene;Acc:145195]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145195","summary":null,"start":104223584,"end":104288069,"strand":1,"description":"chromosome 14 open reading frame 144 [Source:NCBI gene;Acc:145195]"}, {"versioned_ensembl_gene_id":"ENSG00000106993.11","gene_symbol":"CDC37L1","gene_name":"cell division cycle 37 like 1 [Source:HGNC Symbol;Acc:HGNC:17179]","synonyms":"HARC,FLJ20639,CDC37B","biotype":"protein_coding","ncbi_id":"55664","summary":"CDC37L1 is a cytoplasmic phosphoprotein that exists in complex with HSP90 (HSPCA; MIM 140571) as well as several other proteins involved in HSP90-mediated protein folding (Scholz et al., 2001 [PubMed 11413142]).[supplied by OMIM, Mar 2008]","start":4679559,"end":4708398,"strand":1,"description":"cell division cycle 37 like 1 [Source:HGNC Symbol;Acc:HGNC:17179]"}, {"versioned_ensembl_gene_id":"ENSG00000107438.8","gene_symbol":"PDLIM1","gene_name":"PDZ and LIM domain 1 [Source:HGNC Symbol;Acc:HGNC:2067]","synonyms":"hCLIM1,CLP36,CLP-36,CLIM1","biotype":"protein_coding","ncbi_id":"9124","summary":"This gene encodes a member of the enigma protein family. The protein contains two protein interacting domains, a PDZ domain at the amino terminal end and one to three LIM domains at the carboxyl terminal. It is a cytoplasmic protein associated with the cytoskeleton. The protein may function as an adapter to bring other LIM-interacting proteins to the cytoskeleton. Pseudogenes associated with this gene are located on chromosomes 3, 14 and 17. [provided by RefSeq, Oct 2012]","start":95237572,"end":95291024,"strand":-1,"description":"PDZ and LIM domain 1 [Source:HGNC Symbol;Acc:HGNC:2067]"}, {"versioned_ensembl_gene_id":"ENSG00000229110.1","gene_symbol":"AC006355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79124739,"end":79125750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226230.1","gene_symbol":"AC007237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78486530,"end":78487028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257675.1","gene_symbol":"BTBD10P1","gene_name":"BTB domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128678","summary":null,"start":52748776,"end":52750127,"strand":1,"description":"BTB domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51540]"}, {"versioned_ensembl_gene_id":"ENSG00000146618.3","gene_symbol":"FERD3L","gene_name":"Fer3 like bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:16660]","synonyms":"NATO3,N-TWIST,bHLHa31","biotype":"protein_coding","ncbi_id":"222894","summary":null,"start":19144782,"end":19145421,"strand":-1,"description":"Fer3 like bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:16660]"}, {"versioned_ensembl_gene_id":"ENSG00000108599.14","gene_symbol":"AKAP10","gene_name":"A-kinase anchoring protein 10 [Source:HGNC Symbol;Acc:HGNC:368]","synonyms":"PRKA10,MGC9414,D-AKAP2","biotype":"protein_coding","ncbi_id":"11216","summary":"This gene encodes a member of the A-kinase anchor protein family. A-kinase anchor proteins bind to the regulatory subunits of protein kinase A (PKA) and confine the holoenzyme to discrete locations within the cell. The encoded protein is localized to mitochondria and interacts with both the type I and type II regulatory subunits of PKA. Polymorphisms in this gene may be associated with increased risk of arrhythmias and sudden cardiac death. [provided by RefSeq, May 2012]","start":19904302,"end":19978343,"strand":-1,"description":"A-kinase anchoring protein 10 [Source:HGNC Symbol;Acc:HGNC:368]"}, {"versioned_ensembl_gene_id":"ENSG00000236536.1","gene_symbol":"AC003986.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19119933,"end":19121916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255078.1","gene_symbol":"OR4A6P","gene_name":"olfactory receptor family 4 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15163]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390131","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54724847,"end":54725816,"strand":1,"description":"olfactory receptor family 4 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15163]"}, {"versioned_ensembl_gene_id":"ENSG00000125484.11","gene_symbol":"GTF3C4","gene_name":"general transcription factor IIIC subunit 4 [Source:HGNC Symbol;Acc:HGNC:4667]","synonyms":"TFIIIC90,KAT12","biotype":"protein_coding","ncbi_id":"9329","summary":null,"start":132670035,"end":132694955,"strand":1,"description":"general transcription factor IIIC subunit 4 [Source:HGNC Symbol;Acc:HGNC:4667]"}, {"versioned_ensembl_gene_id":"ENSG00000274100.1","gene_symbol":"AL627230.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67721884,"end":67722094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280693.2","gene_symbol":"SH3PXD2A-AS1","gene_name":"SH3PXD2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45242]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505839","summary":null,"start":103745966,"end":103755423,"strand":1,"description":"SH3PXD2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45242]"}, {"versioned_ensembl_gene_id":"ENSG00000243548.3","gene_symbol":"RN7SL101P","gene_name":"RNA, 7SL, cytoplasmic 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:46117]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479260","summary":null,"start":28711198,"end":28711476,"strand":1,"description":"RNA, 7SL, cytoplasmic 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:46117]"}, {"versioned_ensembl_gene_id":"ENSG00000227025.1","gene_symbol":"CR388205.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29996063,"end":29997058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008324.11","gene_symbol":"SS18L2","gene_name":"SS18 like 2 [Source:HGNC Symbol;Acc:HGNC:15593]","synonyms":"KIAA-iso","biotype":"protein_coding","ncbi_id":"51188","summary":"Synovial sarcomas occur most frequently in the extremities around large joints. More than 90% of cases have a recurrent and specific chromosomal translocation, t(X;18)(p11.2;q11.2), in which the 5-prime end of the SS18 gene (MIM 600192) is fused in-frame to the 3-prime end of the SSX1 (MIM 312820), SSX2 (MIM 300192), or SSX4 (MIM 300326) gene. The SS18L2 gene is homologous to SS18.[supplied by OMIM, Jul 2002]","start":42581840,"end":42595114,"strand":1,"description":"SS18 like 2 [Source:HGNC Symbol;Acc:HGNC:15593]"}, {"versioned_ensembl_gene_id":"ENSG00000081377.16","gene_symbol":"CDC14B","gene_name":"cell division cycle 14B [Source:HGNC Symbol;Acc:HGNC:1719]","synonyms":"hCDC14B,CDC14B3,Cdc14B2,Cdc14B1","biotype":"protein_coding","ncbi_id":"8555","summary":"The protein encoded by this gene is a member of the dual specificity protein tyrosine phosphatase family. This protein is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit of cell mitosis and initiation of DNA replication, which suggests the role in cell cycle control. This protein has been shown to interact with and dephosphorylates tumor suppressor protein p53, and is thought to regulate the function of p53. Alternative splice of this gene results in 3 transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":96490241,"end":96619830,"strand":-1,"description":"cell division cycle 14B [Source:HGNC Symbol;Acc:HGNC:1719]"}, {"versioned_ensembl_gene_id":"ENSG00000262721.1","gene_symbol":"AC135048.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":30875766,"end":30895216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232407.3","gene_symbol":"AC104164.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60690225,"end":60690719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205784.2","gene_symbol":"ARRDC5","gene_name":"arrestin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:31407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645432","summary":null,"start":4890437,"end":4902867,"strand":-1,"description":"arrestin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:31407]"}, {"versioned_ensembl_gene_id":"ENSG00000229661.1","gene_symbol":"BUD31P2","gene_name":"BUD31 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480332","summary":null,"start":75201491,"end":75201790,"strand":1,"description":"BUD31 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51562]"}, {"versioned_ensembl_gene_id":"ENSG00000203760.8","gene_symbol":"CENPW","gene_name":"centromere protein W [Source:HGNC Symbol;Acc:HGNC:21488]","synonyms":"CUG2,C6orf173","biotype":"protein_coding","ncbi_id":"387103","summary":null,"start":126340174,"end":126348875,"strand":1,"description":"centromere protein W [Source:HGNC Symbol;Acc:HGNC:21488]"}, {"versioned_ensembl_gene_id":"ENSG00000224584.2","gene_symbol":"UBE2V1P13","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52411]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505982","summary":null,"start":214612960,"end":214613398,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52411]"}, {"versioned_ensembl_gene_id":"ENSG00000077157.21","gene_symbol":"PPP1R12B","gene_name":"protein phosphatase 1 regulatory subunit 12B [Source:HGNC Symbol;Acc:HGNC:7619]","synonyms":"PP1bp55,MYPT2,MGC87886,MGC131980","biotype":"protein_coding","ncbi_id":"4660","summary":"Myosin phosphatase is a protein complex comprised of three subunits: a catalytic subunit (PP1c-delta, protein phosphatase 1, catalytic subunit delta), a large regulatory subunit (MYPT, myosin phosphatase target) and small regulatory subunit (sm-M20). Two isoforms of MYPT have been isolated--MYPT1 and MYPT2, the first of which is widely expressed, and the second of which may be specific to heart, skeletal muscle, and brain. Each of the MYPT isoforms functions to bind PP1c-delta and increase phosphatase activity. This locus encodes both MYTP2 and M20. Alternatively spliced transcript variants encoding different isoforms have been identified. Related pseudogenes have been defined on the Y chromosome. [provided by RefSeq, Oct 2011]","start":202348699,"end":202592706,"strand":1,"description":"protein phosphatase 1 regulatory subunit 12B [Source:HGNC Symbol;Acc:HGNC:7619]"}, {"versioned_ensembl_gene_id":"ENSG00000278735.1","gene_symbol":"AL627230.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67718821,"end":67719022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224263.1","gene_symbol":"CYCSP12","gene_name":"cytochrome c, somatic pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24386]","synonyms":"HCP13,HCP12,CYCSP13","biotype":"processed_pseudogene","ncbi_id":"360168","summary":null,"start":11878830,"end":11879129,"strand":-1,"description":"cytochrome c, somatic pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24386]"}, {"versioned_ensembl_gene_id":"ENSG00000254565.1","gene_symbol":"MTND2P26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42127]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873349","summary":null,"start":103406213,"end":103407241,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42127]"}, {"versioned_ensembl_gene_id":"ENSG00000243167.1","gene_symbol":"RPS10P28","gene_name":"ribosomal protein S10 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35511]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132372","summary":null,"start":42670005,"end":42670816,"strand":1,"description":"ribosomal protein S10 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35511]"}, {"versioned_ensembl_gene_id":"ENSG00000224546.2","gene_symbol":"EIF4BP3","gene_name":"eukaryotic translation initiation factor 4B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128771","summary":null,"start":96146007,"end":96147856,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37936]"}, {"versioned_ensembl_gene_id":"ENSG00000236525.1","gene_symbol":"AC007278.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":102433957,"end":102435340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176695.7","gene_symbol":"OR4F17","gene_name":"olfactory receptor family 4 subfamily F member 17 [Source:HGNC Symbol;Acc:HGNC:15381]","synonyms":"OR4F19,OR4F18,OR4F11P","biotype":"protein_coding","ncbi_id":"81099","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":107104,"end":117102,"strand":1,"description":"olfactory receptor family 4 subfamily F member 17 [Source:HGNC Symbol;Acc:HGNC:15381]"}, {"versioned_ensembl_gene_id":"ENSG00000223932.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31700683,"end":31705737,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000115607.9","gene_symbol":"IL18RAP","gene_name":"interleukin 18 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5989]","synonyms":"CD218b,AcPL","biotype":"protein_coding","ncbi_id":"8807","summary":"The protein encoded by this gene is an accessory subunit of the heterodimeric receptor for interleukin 18 (IL18), a proinflammatory cytokine involved in inducing cell-mediated immunity. This protein enhances the IL18-binding activity of the IL18 receptor and plays a role in signaling by IL18. Mutations in this gene are associated with Crohn's disease and inflammatory bowel disease, and susceptibility to celiac disease and leprosy. Alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]","start":102418689,"end":102452565,"strand":1,"description":"interleukin 18 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5989]"}, {"versioned_ensembl_gene_id":"ENSG00000243295.1","gene_symbol":"AC114400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59065150,"end":59119509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243903.1","gene_symbol":"AC138057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59380024,"end":59388704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242545.1","gene_symbol":"AC126121.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59464330,"end":59510678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201354.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140609847,"end":140609955,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238594.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":150164584,"end":150164686,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000152104.11","gene_symbol":"PTPN14","gene_name":"protein tyrosine phosphatase, non-receptor type 14 [Source:HGNC Symbol;Acc:HGNC:9647]","synonyms":"PEZ","biotype":"protein_coding","ncbi_id":"5784","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N-terminal noncatalytic domain similar to that of band 4.1 superfamily cytoskeleton-associated proteins, which suggested the membrane or cytoskeleton localization of this protein. It appears to regulate lymphatic development in mammals, and a loss of function mutation has been found in a kindred with a lymphedema-choanal atresia. [provided by RefSeq, Sep 2010]","start":214348696,"end":214552449,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 14 [Source:HGNC Symbol;Acc:HGNC:9647]"}, {"versioned_ensembl_gene_id":"ENSG00000163660.11","gene_symbol":"CCNL1","gene_name":"cyclin L1 [Source:HGNC Symbol;Acc:HGNC:20569]","synonyms":"ania-6a","biotype":"protein_coding","ncbi_id":"57018","summary":null,"start":157146508,"end":157160760,"strand":-1,"description":"cyclin L1 [Source:HGNC Symbol;Acc:HGNC:20569]"}, {"versioned_ensembl_gene_id":"ENSG00000241804.1","gene_symbol":"AC126121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59535863,"end":59536415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255042.3","gene_symbol":"AC109635.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50279828,"end":50298452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278643.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11033727,"end":11033912,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000202137.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":201808681,"end":201808782,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206973.1","gene_symbol":"RNU6-1145P","gene_name":"RNA, U6 small nuclear 1145, pseudogene [Source:HGNC Symbol;Acc:HGNC:48108]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481541","summary":null,"start":61605616,"end":61605722,"strand":1,"description":"RNA, U6 small nuclear 1145, pseudogene [Source:HGNC Symbol;Acc:HGNC:48108]"}, {"versioned_ensembl_gene_id":"ENSG00000275868.1","gene_symbol":"MIR8054","gene_name":"microRNA 8054 [Source:HGNC Symbol;Acc:HGNC:50177]","synonyms":"hsa-mir-8054","biotype":"miRNA","ncbi_id":"102465860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23419105,"end":23419190,"strand":-1,"description":"microRNA 8054 [Source:HGNC Symbol;Acc:HGNC:50177]"}, {"versioned_ensembl_gene_id":"ENSG00000200419.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45591984,"end":45592085,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207624.1","gene_symbol":"MIR194-1","gene_name":"microRNA 194-1 [Source:HGNC Symbol;Acc:HGNC:31564]","synonyms":"MIRN194-1,hsa-mir-194-1","biotype":"miRNA","ncbi_id":"406969","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":220118157,"end":220118241,"strand":-1,"description":"microRNA 194-1 [Source:HGNC Symbol;Acc:HGNC:31564]"}, {"versioned_ensembl_gene_id":"ENSG00000265291.1","gene_symbol":"MIR4710","gene_name":"microRNA 4710 [Source:HGNC Symbol;Acc:HGNC:41727]","synonyms":"hsa-mir-4710","biotype":"miRNA","ncbi_id":"100616300","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104677694,"end":104677749,"strand":-1,"description":"microRNA 4710 [Source:HGNC Symbol;Acc:HGNC:41727]"}, {"versioned_ensembl_gene_id":"ENSG00000222472.1","gene_symbol":"RN7SKP7","gene_name":"RNA, 7SK small nuclear pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42625]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873851","summary":null,"start":96949249,"end":96949533,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42625]"}, {"versioned_ensembl_gene_id":"ENSG00000202199.1","gene_symbol":"RNU1-115P","gene_name":"RNA, U1 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48457]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480188","summary":null,"start":133238657,"end":133238816,"strand":-1,"description":"RNA, U1 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48457]"}, {"versioned_ensembl_gene_id":"ENSG00000207622.1","gene_symbol":"MIR619","gene_name":"microRNA 619 [Source:HGNC Symbol;Acc:HGNC:32875]","synonyms":"MIRN619,hsa-mir-619","biotype":"miRNA","ncbi_id":"693204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":108836908,"end":108837006,"strand":-1,"description":"microRNA 619 [Source:HGNC Symbol;Acc:HGNC:32875]"}, {"versioned_ensembl_gene_id":"ENSG00000276398.1","gene_symbol":"RMST_9","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 9 [Source:RFAM;Acc:RF01970]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97560856,"end":97561048,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 9 [Source:RFAM;Acc:RF01970]"}, {"versioned_ensembl_gene_id":"ENSG00000212425.1","gene_symbol":"RNA5SP105","gene_name":"RNA, 5S ribosomal pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:42903]","synonyms":"RN5S105","biotype":"rRNA","ncbi_id":"100873376","summary":null,"start":137512098,"end":137512210,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:42903]"}, {"versioned_ensembl_gene_id":"ENSG00000238924.2","gene_symbol":"RNU7-82P","gene_name":"RNA, U7 small nuclear 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:34178]","synonyms":"U7.82,RNU7-163P","biotype":"snRNA","ncbi_id":"100151679","summary":null,"start":163470205,"end":163470266,"strand":-1,"description":"RNA, U7 small nuclear 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:34178]"}, {"versioned_ensembl_gene_id":"ENSG00000258101.2","gene_symbol":"AC010173.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49232790,"end":49264756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283818.1","gene_symbol":"MIR7844","gene_name":"microRNA 7844 [Source:HGNC Symbol;Acc:HGNC:50044]","synonyms":"hsa-mir-7844","biotype":"miRNA","ncbi_id":"102465834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94571231,"end":94571352,"strand":-1,"description":"microRNA 7844 [Source:HGNC Symbol;Acc:HGNC:50044]"}, {"versioned_ensembl_gene_id":"ENSG00000201270.1","gene_symbol":"RNU6-755P","gene_name":"RNA, U6 small nuclear 755, pseudogene [Source:HGNC Symbol;Acc:HGNC:47718]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481915","summary":null,"start":164980035,"end":164980137,"strand":-1,"description":"RNA, U6 small nuclear 755, pseudogene [Source:HGNC Symbol;Acc:HGNC:47718]"}, {"versioned_ensembl_gene_id":"ENSG00000201595.1","gene_symbol":"RNA5SP132","gene_name":"RNA, 5S ribosomal pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:43032]","synonyms":"RN5S132","biotype":"rRNA","ncbi_id":"100873401","summary":null,"start":51694465,"end":51694582,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:43032]"}, {"versioned_ensembl_gene_id":"ENSG00000221638.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":75627950,"end":75628168,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000284416.1","gene_symbol":"MIR1908","gene_name":"microRNA 1908 [Source:HGNC Symbol;Acc:HGNC:35392]","synonyms":"MIRN1908,hsa-mir-1908","biotype":"miRNA","ncbi_id":"100302263","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61815161,"end":61815240,"strand":-1,"description":"microRNA 1908 [Source:HGNC Symbol;Acc:HGNC:35392]"}, {"versioned_ensembl_gene_id":"ENSG00000265407.1","gene_symbol":"MIR4324","gene_name":"microRNA 4324 [Source:HGNC Symbol;Acc:HGNC:38392]","synonyms":"hsa-mir-4324","biotype":"miRNA","ncbi_id":"100422979","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49308797,"end":49308868,"strand":-1,"description":"microRNA 4324 [Source:HGNC Symbol;Acc:HGNC:38392]"}, {"versioned_ensembl_gene_id":"ENSG00000201309.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":134283092,"end":134283193,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281859.1","gene_symbol":"SNORD38B","gene_name":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]","synonyms":"U38B,RNU38B,U38B,RNU38B","biotype":"snoRNA","ncbi_id":"94163","summary":null,"start":44778390,"end":44778458,"strand":1,"description":"small nucleolar RNA, C/D box 38B [Source:HGNC Symbol;Acc:HGNC:30356]"}, {"versioned_ensembl_gene_id":"ENSG00000200256.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75835215,"end":75835323,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251750.1","gene_symbol":"RNU5F-8P","gene_name":"RNA, U5F small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42531]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873839","summary":null,"start":240653367,"end":240653477,"strand":1,"description":"RNA, U5F small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42531]"}, {"versioned_ensembl_gene_id":"ENSG00000273829.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50054143,"end":50054430,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000239039.1","gene_symbol":"SNORD13","gene_name":"small nucleolar RNA, C/D box 13 [Source:HGNC Symbol;Acc:HGNC:32711]","synonyms":"U13,SNORD13A,RNU13","biotype":"snoRNA","ncbi_id":"692084","summary":null,"start":33513475,"end":33513578,"strand":1,"description":"small nucleolar RNA, C/D box 13 [Source:HGNC Symbol;Acc:HGNC:32711]"}, {"versioned_ensembl_gene_id":"ENSG00000202360.1","gene_symbol":"RN7SKP249","gene_name":"RNA, 7SK small nuclear pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:45973]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480910","summary":null,"start":101137959,"end":101138313,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 249 [Source:HGNC Symbol;Acc:HGNC:45973]"}, {"versioned_ensembl_gene_id":"ENSG00000200719.1","gene_symbol":"RNA5SP260","gene_name":"RNA, 5S ribosomal pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:43160]","synonyms":"RN5S260","biotype":"rRNA","ncbi_id":"100873514","summary":null,"start":29048494,"end":29048604,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:43160]"}, {"versioned_ensembl_gene_id":"ENSG00000251998.1","gene_symbol":"RNU6-168P","gene_name":"RNA, U6 small nuclear 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:47131]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479640","summary":null,"start":163796065,"end":163796165,"strand":-1,"description":"RNA, U6 small nuclear 168, pseudogene [Source:HGNC Symbol;Acc:HGNC:47131]"}, {"versioned_ensembl_gene_id":"ENSG00000278257.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000199362.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75837544,"end":75837645,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252914.1","gene_symbol":"RNU6-789P","gene_name":"RNA, U6 small nuclear 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:47752]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479915","summary":null,"start":136721394,"end":136721495,"strand":-1,"description":"RNA, U6 small nuclear 789, pseudogene [Source:HGNC Symbol;Acc:HGNC:47752]"}, {"versioned_ensembl_gene_id":"ENSG00000199567.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":86019608,"end":86019715,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273866.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37578669,"end":37578922,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199631.1","gene_symbol":"SNORD33","gene_name":"small nucleolar RNA, C/D box 33 [Source:HGNC Symbol;Acc:HGNC:10160]","synonyms":"U33,RNU33","biotype":"snoRNA","ncbi_id":"26818","summary":null,"start":49490615,"end":49490699,"strand":1,"description":"small nucleolar RNA, C/D box 33 [Source:HGNC Symbol;Acc:HGNC:10160]"}, {"versioned_ensembl_gene_id":"ENSG00000212516.1","gene_symbol":"RNU6-1268P","gene_name":"RNA, U6 small nuclear 1268, pseudogene [Source:HGNC Symbol;Acc:HGNC:48231]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480654","summary":null,"start":19422815,"end":19422921,"strand":-1,"description":"RNA, U6 small nuclear 1268, pseudogene [Source:HGNC Symbol;Acc:HGNC:48231]"}, {"versioned_ensembl_gene_id":"ENSG00000253063.1","gene_symbol":"RNU6-494P","gene_name":"RNA, U6 small nuclear 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:47457]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479785","summary":null,"start":32477382,"end":32477471,"strand":-1,"description":"RNA, U6 small nuclear 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:47457]"}, {"versioned_ensembl_gene_id":"ENSG00000273715.4","gene_symbol":"AC138827.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70150924,"end":70167868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238705.1","gene_symbol":"MIR1976","gene_name":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]","synonyms":"hsa-mir-1976","biotype":"miRNA","ncbi_id":"100302190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26554542,"end":26554593,"strand":1,"description":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]"}, {"versioned_ensembl_gene_id":"ENSG00000200526.1","gene_symbol":"RNY4P14","gene_name":"RNA, Ro-associated Y4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:34064]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379584","summary":null,"start":39785415,"end":39785510,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:34064]"}, {"versioned_ensembl_gene_id":"ENSG00000200986.1","gene_symbol":"RNU6-819P","gene_name":"RNA, U6 small nuclear 819, pseudogene [Source:HGNC Symbol;Acc:HGNC:47782]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479928","summary":null,"start":47131781,"end":47131887,"strand":-1,"description":"RNA, U6 small nuclear 819, pseudogene [Source:HGNC Symbol;Acc:HGNC:47782]"}, {"versioned_ensembl_gene_id":"ENSG00000212221.1","gene_symbol":"RNU6-220P","gene_name":"RNA, U6 small nuclear 220, pseudogene [Source:HGNC Symbol;Acc:HGNC:47183]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481247","summary":null,"start":143350172,"end":143350278,"strand":1,"description":"RNA, U6 small nuclear 220, pseudogene [Source:HGNC Symbol;Acc:HGNC:47183]"}, {"versioned_ensembl_gene_id":"ENSG00000201331.1","gene_symbol":"SNORD115-23","gene_name":"small nucleolar RNA, C/D box 115-23 [Source:HGNC Symbol;Acc:HGNC:33042]","synonyms":"HBII-52-23","biotype":"snoRNA","ncbi_id":"100033800","summary":null,"start":25211796,"end":25211877,"strand":1,"description":"small nucleolar RNA, C/D box 115-23 [Source:HGNC Symbol;Acc:HGNC:33042]"}, {"versioned_ensembl_gene_id":"ENSG00000239189.1","gene_symbol":"RNU6-634P","gene_name":"RNA, U6 small nuclear 634, pseudogene [Source:HGNC Symbol;Acc:HGNC:47597]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479847","summary":null,"start":55499950,"end":55500055,"strand":1,"description":"RNA, U6 small nuclear 634, pseudogene [Source:HGNC Symbol;Acc:HGNC:47597]"}, {"versioned_ensembl_gene_id":"ENSG00000272230.1","gene_symbol":"MIR3666","gene_name":"microRNA 3666 [Source:HGNC Symbol;Acc:HGNC:38940]","synonyms":"hsa-mir-3666","biotype":"miRNA","ncbi_id":"100500896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114653345,"end":114653455,"strand":1,"description":"microRNA 3666 [Source:HGNC Symbol;Acc:HGNC:38940]"}, {"versioned_ensembl_gene_id":"ENSG00000274848.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30816030,"end":30816302,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275455.1","gene_symbol":"MIR7852","gene_name":"microRNA 7852 [Source:HGNC Symbol;Acc:HGNC:50201]","synonyms":"hsa-mir-7852","biotype":"miRNA","ncbi_id":"102465839","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":107897223,"end":107897304,"strand":1,"description":"microRNA 7852 [Source:HGNC Symbol;Acc:HGNC:50201]"}, {"versioned_ensembl_gene_id":"ENSG00000275502.1","gene_symbol":"DAOA-AS1_2","gene_name":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105462302,"end":105462505,"strand":1,"description":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]"}, {"versioned_ensembl_gene_id":"ENSG00000207941.1","gene_symbol":"MIR552","gene_name":"microRNA 552 [Source:HGNC Symbol;Acc:HGNC:32808]","synonyms":"MIRN552,hsa-mir-552","biotype":"miRNA","ncbi_id":"693137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34669599,"end":34669694,"strand":-1,"description":"microRNA 552 [Source:HGNC Symbol;Acc:HGNC:32808]"}, {"versioned_ensembl_gene_id":"ENSG00000238584.1","gene_symbol":"RNU7-167P","gene_name":"RNA, U7 small nuclear 167 pseudogene [Source:HGNC Symbol;Acc:HGNC:45701]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479088","summary":null,"start":35249772,"end":35249833,"strand":1,"description":"RNA, U7 small nuclear 167 pseudogene [Source:HGNC Symbol;Acc:HGNC:45701]"}, {"versioned_ensembl_gene_id":"ENSG00000207938.1","gene_symbol":"MIR511","gene_name":"microRNA 511 [Source:HGNC Symbol;Acc:HGNC:32077]","synonyms":"hsa-mir-511-2,hsa-mir-511-1,MIRN511-2,MIRN511-1,MIR511-2,MIR511-1","biotype":"miRNA","ncbi_id":"574445","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17845107,"end":17845193,"strand":1,"description":"microRNA 511 [Source:HGNC Symbol;Acc:HGNC:32077]"}, {"versioned_ensembl_gene_id":"ENSG00000269167.1","gene_symbol":"CR753845.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31988350,"end":31989286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269651.1","gene_symbol":"AC022146.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8173272,"end":8175567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284029.1","gene_symbol":"MIR6805","gene_name":"microRNA 6805 [Source:HGNC Symbol;Acc:HGNC:50215]","synonyms":"hsa-mir-6805","biotype":"miRNA","ncbi_id":"102465483","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55388181,"end":55388242,"strand":1,"description":"microRNA 6805 [Source:HGNC Symbol;Acc:HGNC:50215]"}, {"versioned_ensembl_gene_id":"ENSG00000276532.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18605054,"end":18605356,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000221065.1","gene_symbol":"MIR1233-2","gene_name":"microRNA 1233-2 [Source:HGNC Symbol;Acc:HGNC:38277]","synonyms":"hsa-mir-1233-2","biotype":"miRNA","ncbi_id":"100422845","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34528290,"end":34528371,"strand":-1,"description":"microRNA 1233-2 [Source:HGNC Symbol;Acc:HGNC:38277]"}, {"versioned_ensembl_gene_id":"ENSG00000274621.1","gene_symbol":"MIR6867","gene_name":"microRNA 6867 [Source:HGNC Symbol;Acc:HGNC:50134]","synonyms":"hsa-mir-6867","biotype":"miRNA","ncbi_id":"102465523","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40193597,"end":40193663,"strand":1,"description":"microRNA 6867 [Source:HGNC Symbol;Acc:HGNC:50134]"}, {"versioned_ensembl_gene_id":"ENSG00000275399.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"CLR19.9,NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54972989,"end":55008845,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000266072.1","gene_symbol":"MIR5693","gene_name":"microRNA 5693 [Source:HGNC Symbol;Acc:HGNC:43499]","synonyms":"hsa-mir-5693","biotype":"miRNA","ncbi_id":"100847003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51348567,"end":51348639,"strand":-1,"description":"microRNA 5693 [Source:HGNC Symbol;Acc:HGNC:43499]"}, {"versioned_ensembl_gene_id":"ENSG00000264501.2","gene_symbol":"RN7SL731P","gene_name":"RNA, 7SL, cytoplasmic 731, pseudogene [Source:HGNC Symbol;Acc:HGNC:46747]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107048981","summary":null,"start":10306465,"end":10306757,"strand":1,"description":"RNA, 7SL, cytoplasmic 731, pseudogene [Source:HGNC Symbol;Acc:HGNC:46747]"}, {"versioned_ensembl_gene_id":"ENSG00000278365.1","gene_symbol":"AC012314.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238789.1","gene_symbol":"RNU7-152P","gene_name":"RNA, U7 small nuclear 152 pseudogene [Source:HGNC Symbol;Acc:HGNC:45686]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479081","summary":null,"start":155654963,"end":155655026,"strand":-1,"description":"RNA, U7 small nuclear 152 pseudogene [Source:HGNC Symbol;Acc:HGNC:45686]"}, {"versioned_ensembl_gene_id":"ENSG00000207205.1","gene_symbol":"RNVU1-15","gene_name":"RNA, variant U1 small nuclear 15 [Source:HGNC Symbol;Acc:HGNC:48320]","synonyms":"RNU1-121,vU1.16,vU1.15,RNVU1-16,RNU1-66","biotype":"snRNA","ncbi_id":"101954267","summary":null,"start":144412576,"end":144412740,"strand":1,"description":"RNA, variant U1 small nuclear 15 [Source:HGNC Symbol;Acc:HGNC:48320]"}, {"versioned_ensembl_gene_id":"ENSG00000277578.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":84642487,"end":84642763,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202035.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73403788,"end":73403889,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199803.1","gene_symbol":"RNU6-1159P","gene_name":"RNA, U6 small nuclear 1159, pseudogene [Source:HGNC Symbol;Acc:HGNC:48122]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481939","summary":null,"start":15021553,"end":15021659,"strand":-1,"description":"RNA, U6 small nuclear 1159, pseudogene [Source:HGNC Symbol;Acc:HGNC:48122]"}, {"versioned_ensembl_gene_id":"ENSG00000222796.1","gene_symbol":"RNU6-383P","gene_name":"RNA, U6 small nuclear 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:47346]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479736","summary":null,"start":150955494,"end":150955587,"strand":-1,"description":"RNA, U6 small nuclear 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:47346]"}, {"versioned_ensembl_gene_id":"ENSG00000159335.15","gene_symbol":"PTMS","gene_name":"parathymosin [Source:HGNC Symbol;Acc:HGNC:9629]","synonyms":"ParaT","biotype":"protein_coding","ncbi_id":"5763","summary":null,"start":6765516,"end":6770952,"strand":1,"description":"parathymosin [Source:HGNC Symbol;Acc:HGNC:9629]"}, {"versioned_ensembl_gene_id":"ENSG00000198976.1","gene_symbol":"MIR429","gene_name":"microRNA 429 [Source:HGNC Symbol;Acc:HGNC:13784]","synonyms":"MIRN429,hsa-mir-429","biotype":"miRNA","ncbi_id":"554210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1169005,"end":1169087,"strand":1,"description":"microRNA 429 [Source:HGNC Symbol;Acc:HGNC:13784]"}, {"versioned_ensembl_gene_id":"ENSG00000274293.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38150050,"end":38150138,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000200587.1","gene_symbol":"RNA5SP514","gene_name":"RNA, 5S ribosomal pseudogene 514 [Source:HGNC Symbol;Acc:HGNC:43414]","synonyms":"RN5S514","biotype":"rRNA","ncbi_id":"100873565","summary":null,"start":131938846,"end":131938956,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 514 [Source:HGNC Symbol;Acc:HGNC:43414]"}, {"versioned_ensembl_gene_id":"ENSG00000212545.1","gene_symbol":"RNU6-337P","gene_name":"RNA, U6 small nuclear 337, pseudogene [Source:HGNC Symbol;Acc:HGNC:47300]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479716","summary":null,"start":79030240,"end":79030345,"strand":1,"description":"RNA, U6 small nuclear 337, pseudogene [Source:HGNC Symbol;Acc:HGNC:47300]"}, {"versioned_ensembl_gene_id":"ENSG00000199712.1","gene_symbol":"SNORD115-2","gene_name":"small nucleolar RNA, C/D box 115-2 [Source:HGNC Symbol;Acc:HGNC:33021]","synonyms":"HBII-52-2","biotype":"snoRNA","ncbi_id":"100033437","summary":null,"start":25172635,"end":25172716,"strand":1,"description":"small nucleolar RNA, C/D box 115-2 [Source:HGNC Symbol;Acc:HGNC:33021]"}, {"versioned_ensembl_gene_id":"ENSG00000222202.1","gene_symbol":"RNU4-26P","gene_name":"RNA, U4 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46962]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479569","summary":null,"start":20418321,"end":20418427,"strand":1,"description":"RNA, U4 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46962]"}, {"versioned_ensembl_gene_id":"ENSG00000221533.1","gene_symbol":"MIR1184-1","gene_name":"microRNA 1184-1 [Source:HGNC Symbol;Acc:HGNC:35265]","synonyms":"MIRN1184,MIR1184,hsa-mir-1184","biotype":"miRNA","ncbi_id":"100302111","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154887360,"end":154887458,"strand":-1,"description":"microRNA 1184-1 [Source:HGNC Symbol;Acc:HGNC:35265]"}, {"versioned_ensembl_gene_id":"ENSG00000265347.1","gene_symbol":"MIR4291","gene_name":"microRNA 4291 [Source:HGNC Symbol;Acc:HGNC:38267]","synonyms":"hsa-mir-4291","biotype":"miRNA","ncbi_id":"100422927","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93819357,"end":93819421,"strand":1,"description":"microRNA 4291 [Source:HGNC Symbol;Acc:HGNC:38267]"}, {"versioned_ensembl_gene_id":"ENSG00000263790.1","gene_symbol":"MIR4473","gene_name":"microRNA 4473 [Source:HGNC Symbol;Acc:HGNC:41540]","synonyms":"hsa-mir-4473","biotype":"miRNA","ncbi_id":"100616229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20411148,"end":20411238,"strand":-1,"description":"microRNA 4473 [Source:HGNC Symbol;Acc:HGNC:41540]"}, {"versioned_ensembl_gene_id":"ENSG00000223259.1","gene_symbol":"RNA5SP508","gene_name":"RNA, 5S ribosomal pseudogene 508 [Source:HGNC Symbol;Acc:HGNC:43408]","synonyms":"RN5S508","biotype":"rRNA","ncbi_id":"100873559","summary":null,"start":76655009,"end":76655127,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 508 [Source:HGNC Symbol;Acc:HGNC:43408]"}, {"versioned_ensembl_gene_id":"ENSG00000202308.1","gene_symbol":"RNU6-996P","gene_name":"RNA, U6 small nuclear 996, pseudogene [Source:HGNC Symbol;Acc:HGNC:47959]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481928","summary":null,"start":107663140,"end":107663246,"strand":-1,"description":"RNA, U6 small nuclear 996, pseudogene [Source:HGNC Symbol;Acc:HGNC:47959]"}, {"versioned_ensembl_gene_id":"ENSG00000274740.1","gene_symbol":"AC013791.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2871437,"end":2871498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221063.3","gene_symbol":"MIR1296","gene_name":"microRNA 1296 [Source:HGNC Symbol;Acc:HGNC:35249]","synonyms":"MIRN1296,hsa-mir-1296","biotype":"miRNA","ncbi_id":"100302150","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63372957,"end":63373048,"strand":-1,"description":"microRNA 1296 [Source:HGNC Symbol;Acc:HGNC:35249]"}, {"versioned_ensembl_gene_id":"ENSG00000199936.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85460144,"end":85460252,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200279.1","gene_symbol":"SNORD114-10","gene_name":"small nucleolar RNA, C/D box 114-10 [Source:HGNC Symbol;Acc:HGNC:32998]","synonyms":"14q(II-10)","biotype":"snoRNA","ncbi_id":"767588","summary":null,"start":100967052,"end":100967123,"strand":1,"description":"small nucleolar RNA, C/D box 114-10 [Source:HGNC Symbol;Acc:HGNC:32998]"}, {"versioned_ensembl_gene_id":"ENSG00000265919.1","gene_symbol":"MIR4280","gene_name":"microRNA 4280 [Source:HGNC Symbol;Acc:HGNC:38334]","synonyms":"hsa-mir-4280","biotype":"miRNA","ncbi_id":"100422887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87114879,"end":87114954,"strand":-1,"description":"microRNA 4280 [Source:HGNC Symbol;Acc:HGNC:38334]"}, {"versioned_ensembl_gene_id":"ENSG00000207784.3","gene_symbol":"MIR542","gene_name":"microRNA 542 [Source:HGNC Symbol;Acc:HGNC:32534]","synonyms":"MIRN542,hsa-mir-542","biotype":"miRNA","ncbi_id":"664617","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134541341,"end":134541437,"strand":-1,"description":"microRNA 542 [Source:HGNC Symbol;Acc:HGNC:32534]"}, {"versioned_ensembl_gene_id":"ENSG00000252658.1","gene_symbol":"RNU6-786P","gene_name":"RNA, U6 small nuclear 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:47749]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481429","summary":null,"start":157934168,"end":157934257,"strand":1,"description":"RNA, U6 small nuclear 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:47749]"}, {"versioned_ensembl_gene_id":"ENSG00000274306.1","gene_symbol":"MIR5088","gene_name":"microRNA 5088 [Source:HGNC Symbol;Acc:HGNC:43489]","synonyms":"hsa-mir-5088","biotype":"miRNA","ncbi_id":"100847074","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49682117,"end":49682195,"strand":1,"description":"microRNA 5088 [Source:HGNC Symbol;Acc:HGNC:43489]"}, {"versioned_ensembl_gene_id":"ENSG00000252970.1","gene_symbol":"RNA5SP159","gene_name":"RNA, 5S ribosomal pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:43059]","synonyms":"RN5S159","biotype":"rRNA","ncbi_id":"100873425","summary":null,"start":39936753,"end":39936855,"strand":1,"description":"RNA, 5S ribosomal pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:43059]"}, {"versioned_ensembl_gene_id":"ENSG00000283152.1","gene_symbol":"MIR3120","gene_name":"microRNA 3120 [Source:HGNC Symbol;Acc:HGNC:38295]","synonyms":"hsa-mir-3120","biotype":"miRNA","ncbi_id":"100422882","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":172138808,"end":172138888,"strand":1,"description":"microRNA 3120 [Source:HGNC Symbol;Acc:HGNC:38295]"}, {"versioned_ensembl_gene_id":"ENSG00000264803.1","gene_symbol":"MIR378C","gene_name":"microRNA 378c [Source:HGNC Symbol;Acc:HGNC:38374]","synonyms":"hsa-mir-378c","biotype":"miRNA","ncbi_id":"100422867","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130962588,"end":130962668,"strand":-1,"description":"microRNA 378c [Source:HGNC Symbol;Acc:HGNC:38374]"}, {"versioned_ensembl_gene_id":"ENSG00000201517.1","gene_symbol":"RNU6-707P","gene_name":"RNA, U6 small nuclear 707, pseudogene [Source:HGNC Symbol;Acc:HGNC:47670]","synonyms":null,"biotype":"snRNA","ncbi_id":"107075318","summary":null,"start":48153980,"end":48154074,"strand":-1,"description":"RNA, U6 small nuclear 707, pseudogene [Source:HGNC Symbol;Acc:HGNC:47670]"}, {"versioned_ensembl_gene_id":"ENSG00000221662.1","gene_symbol":"MIR1290","gene_name":"microRNA 1290 [Source:HGNC Symbol;Acc:HGNC:35283]","synonyms":"MIRN1290,hsa-mir-1290","biotype":"miRNA","ncbi_id":"100302276","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18897071,"end":18897148,"strand":-1,"description":"microRNA 1290 [Source:HGNC Symbol;Acc:HGNC:35283]"}, {"versioned_ensembl_gene_id":"ENSG00000109762.15","gene_symbol":"SNX25","gene_name":"sorting nexin 25 [Source:HGNC Symbol;Acc:HGNC:21883]","synonyms":"SBBI31","biotype":"protein_coding","ncbi_id":"83891","summary":null,"start":185204237,"end":185370185,"strand":1,"description":"sorting nexin 25 [Source:HGNC Symbol;Acc:HGNC:21883]"}, {"versioned_ensembl_gene_id":"ENSG00000278378.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000252721.1","gene_symbol":"RNU6-798P","gene_name":"RNA, U6 small nuclear 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:47761]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479919","summary":null,"start":97192923,"end":97193025,"strand":-1,"description":"RNA, U6 small nuclear 798, pseudogene [Source:HGNC Symbol;Acc:HGNC:47761]"}, {"versioned_ensembl_gene_id":"ENSG00000265281.1","gene_symbol":"MIR3935","gene_name":"microRNA 3935 [Source:HGNC Symbol;Acc:HGNC:38918]","synonyms":"hsa-mir-3935","biotype":"miRNA","ncbi_id":"100500891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56245520,"end":56245623,"strand":1,"description":"microRNA 3935 [Source:HGNC Symbol;Acc:HGNC:38918]"}, {"versioned_ensembl_gene_id":"ENSG00000273657.1","gene_symbol":"MIR6792","gene_name":"microRNA 6792 [Source:HGNC Symbol;Acc:HGNC:50054]","synonyms":"hsa-mir-6792","biotype":"miRNA","ncbi_id":"102465475","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7617439,"end":7617505,"strand":1,"description":"microRNA 6792 [Source:HGNC Symbol;Acc:HGNC:50054]"}, {"versioned_ensembl_gene_id":"ENSG00000284246.1","gene_symbol":"MIR6716","gene_name":"microRNA 6716 [Source:HGNC Symbol;Acc:HGNC:50048]","synonyms":"hsa-mir-6716","biotype":"miRNA","ncbi_id":"102466719","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":118644000,"end":118644079,"strand":1,"description":"microRNA 6716 [Source:HGNC Symbol;Acc:HGNC:50048]"}, {"versioned_ensembl_gene_id":"ENSG00000277580.1","gene_symbol":"RNU6-747P","gene_name":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480399","summary":null,"start":243081156,"end":243081259,"strand":-1,"description":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]"}, {"versioned_ensembl_gene_id":"ENSG00000276839.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":182576772,"end":182577040,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222389.1","gene_symbol":"RNU2-28P","gene_name":"RNA, U2 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:48521]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480670","summary":null,"start":81509476,"end":81509664,"strand":1,"description":"RNA, U2 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:48521]"}, {"versioned_ensembl_gene_id":"ENSG00000275134.1","gene_symbol":"MEG8_2","gene_name":"Maternally expressed 8 exon 2 [Source:RFAM;Acc:RF02146]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100898958,"end":100899079,"strand":1,"description":"Maternally expressed 8 exon 2 [Source:RFAM;Acc:RF02146]"}, {"versioned_ensembl_gene_id":"ENSG00000252143.1","gene_symbol":"SCARNA17","gene_name":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]","synonyms":"U91,mgU12-22/U4-8","biotype":"scaRNA","ncbi_id":"677769","summary":null,"start":21544897,"end":21545039,"strand":1,"description":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]"}, {"versioned_ensembl_gene_id":"ENSG00000206620.1","gene_symbol":"SNORD45C","gene_name":"small nucleolar RNA, C/D box 45C [Source:HGNC Symbol;Acc:HGNC:32720]","synonyms":"U45C","biotype":"snoRNA","ncbi_id":"692085","summary":null,"start":75787072,"end":75787150,"strand":1,"description":"small nucleolar RNA, C/D box 45C [Source:HGNC Symbol;Acc:HGNC:32720]"}, {"versioned_ensembl_gene_id":"ENSG00000200113.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":37419628,"end":37419767,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000277467.1","gene_symbol":"RN7SL628P","gene_name":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479451","summary":null,"start":30612724,"end":30612960,"strand":1,"description":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]"}, {"versioned_ensembl_gene_id":"ENSG00000221025.1","gene_symbol":"MIR1250","gene_name":"microRNA 1250 [Source:HGNC Symbol;Acc:HGNC:35316]","synonyms":"MIRN1250,hsa-mir-1250","biotype":"miRNA","ncbi_id":"100302229","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81133196,"end":81133308,"strand":-1,"description":"microRNA 1250 [Source:HGNC Symbol;Acc:HGNC:35316]"}, {"versioned_ensembl_gene_id":"ENSG00000207442.1","gene_symbol":"SNORD116-6","gene_name":"small nucleolar RNA, C/D box 116-6 [Source:HGNC Symbol;Acc:HGNC:33072]","synonyms":"HBII-85-6","biotype":"snoRNA","ncbi_id":"100033418","summary":null,"start":25065026,"end":25065121,"strand":1,"description":"small nucleolar RNA, C/D box 116-6 [Source:HGNC Symbol;Acc:HGNC:33072]"}, {"versioned_ensembl_gene_id":"ENSG00000241739.1","gene_symbol":"AC010469.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31840492,"end":31840971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274340.1","gene_symbol":"AC032011.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62387327,"end":62388875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266655.1","gene_symbol":"MIR3908","gene_name":"microRNA 3908 [Source:HGNC Symbol;Acc:HGNC:38991]","synonyms":"hsa-mir-3908","biotype":"miRNA","ncbi_id":"100500909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123536409,"end":123536534,"strand":1,"description":"microRNA 3908 [Source:HGNC Symbol;Acc:HGNC:38991]"}, {"versioned_ensembl_gene_id":"ENSG00000273500.1","gene_symbol":"MIR6129","gene_name":"microRNA 6129 [Source:HGNC Symbol;Acc:HGNC:50220]","synonyms":"hsa-mir-6129","biotype":"miRNA","ncbi_id":"102465137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49288346,"end":49288454,"strand":-1,"description":"microRNA 6129 [Source:HGNC Symbol;Acc:HGNC:50220]"}, {"versioned_ensembl_gene_id":"ENSG00000274988.1","gene_symbol":"MIR6876","gene_name":"microRNA 6876 [Source:HGNC Symbol;Acc:HGNC:50181]","synonyms":"hsa-mir-6876","biotype":"miRNA","ncbi_id":"102465527","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25345402,"end":25345474,"strand":1,"description":"microRNA 6876 [Source:HGNC Symbol;Acc:HGNC:50181]"}, {"versioned_ensembl_gene_id":"ENSG00000199085.3","gene_symbol":"MIR148A","gene_name":"microRNA 148a [Source:HGNC Symbol;Acc:HGNC:31535]","synonyms":"MIRN148A,MIRN148,hsa-mir-148a,hsa-mir-148","biotype":"miRNA","ncbi_id":"406940","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25949919,"end":25949986,"strand":-1,"description":"microRNA 148a [Source:HGNC Symbol;Acc:HGNC:31535]"}, {"versioned_ensembl_gene_id":"ENSG00000240183.3","gene_symbol":"RN7SL297P","gene_name":"RNA, 7SL, cytoplasmic 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:46313]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479330","summary":null,"start":111930175,"end":111930467,"strand":1,"description":"RNA, 7SL, cytoplasmic 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:46313]"}, {"versioned_ensembl_gene_id":"ENSG00000265527.1","gene_symbol":"MIR5690","gene_name":"microRNA 5690 [Source:HGNC Symbol;Acc:HGNC:43490]","synonyms":"hsa-mir-5690","biotype":"miRNA","ncbi_id":"100847048","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35664717,"end":35664789,"strand":-1,"description":"microRNA 5690 [Source:HGNC Symbol;Acc:HGNC:43490]"}, {"versioned_ensembl_gene_id":"ENSG00000221737.1","gene_symbol":"MIR548I1","gene_name":"microRNA 548i-1 [Source:HGNC Symbol;Acc:HGNC:35352]","synonyms":"MIRN548I1,hsa-mir-548i-1","biotype":"miRNA","ncbi_id":"100302204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125790404,"end":125790552,"strand":-1,"description":"microRNA 548i-1 [Source:HGNC Symbol;Acc:HGNC:35352]"}, {"versioned_ensembl_gene_id":"ENSG00000278525.1","gene_symbol":"RN7SL607P","gene_name":"RNA, 7SL, cytoplasmic 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:46623]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481088","summary":null,"start":20738433,"end":20738731,"strand":-1,"description":"RNA, 7SL, cytoplasmic 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:46623]"}, {"versioned_ensembl_gene_id":"ENSG00000252620.1","gene_symbol":"RNU6ATAC24P","gene_name":"RNA, U6atac small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:46923]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479554","summary":null,"start":195523087,"end":195523221,"strand":-1,"description":"RNA, U6atac small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:46923]"}, {"versioned_ensembl_gene_id":"ENSG00000267379.1","gene_symbol":"AC008569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14402717,"end":14408723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270830.1","gene_symbol":"AC022441.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50903608,"end":50903743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283513.1","gene_symbol":"MIR941-3","gene_name":"microRNA 941-3 [Source:HGNC Symbol;Acc:HGNC:33686]","synonyms":"MIRN941-3,hsa-mir-941-3","biotype":"miRNA","ncbi_id":"100126352","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919561,"end":63919632,"strand":1,"description":"microRNA 941-3 [Source:HGNC Symbol;Acc:HGNC:33686]"}, {"versioned_ensembl_gene_id":"ENSG00000199017.2","gene_symbol":"MIR1-1","gene_name":"microRNA 1-1 [Source:HGNC Symbol;Acc:HGNC:31499]","synonyms":"MIRN1-1,hsa-mir-1-1","biotype":"miRNA","ncbi_id":"406904","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62554306,"end":62554376,"strand":1,"description":"microRNA 1-1 [Source:HGNC Symbol;Acc:HGNC:31499]"}, {"versioned_ensembl_gene_id":"ENSG00000284331.1","gene_symbol":"MIR4741","gene_name":"microRNA 4741 [Source:HGNC Symbol;Acc:HGNC:41661]","synonyms":"hsa-mir-4741","biotype":"miRNA","ncbi_id":"100616139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22933349,"end":22933438,"strand":1,"description":"microRNA 4741 [Source:HGNC Symbol;Acc:HGNC:41661]"}, {"versioned_ensembl_gene_id":"ENSG00000264722.1","gene_symbol":"MIR3670-2","gene_name":"microRNA 3670-2 [Source:HGNC Symbol;Acc:HGNC:43460]","synonyms":"hsa-mir-3670-2","biotype":"miRNA","ncbi_id":"100846994","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16306370,"end":16306434,"strand":1,"description":"microRNA 3670-2 [Source:HGNC Symbol;Acc:HGNC:43460]"}, {"versioned_ensembl_gene_id":"ENSG00000200060.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108738484,"end":108738604,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207742.3","gene_symbol":"MIR487A","gene_name":"microRNA 487a [Source:HGNC Symbol;Acc:HGNC:32343]","synonyms":"MIRN487A,MIRN487,hsa-mir-487a,hsa-mir-487","biotype":"miRNA","ncbi_id":"619555","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101052446,"end":101052525,"strand":1,"description":"microRNA 487a [Source:HGNC Symbol;Acc:HGNC:32343]"}, {"versioned_ensembl_gene_id":"ENSG00000207244.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":8961575,"end":8961708,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000252734.1","gene_symbol":"RNU6-980P","gene_name":"RNA, U6 small nuclear 980, pseudogene [Source:HGNC Symbol;Acc:HGNC:47943]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481489","summary":null,"start":53732981,"end":53733083,"strand":-1,"description":"RNA, U6 small nuclear 980, pseudogene [Source:HGNC Symbol;Acc:HGNC:47943]"}, {"versioned_ensembl_gene_id":"ENSG00000200028.1","gene_symbol":"RNA5SP98","gene_name":"RNA, 5S ribosomal pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:42896]","synonyms":"RN5S98","biotype":"rRNA","ncbi_id":"100873331","summary":null,"start":76772909,"end":76773045,"strand":1,"description":"RNA, 5S ribosomal pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:42896]"}, {"versioned_ensembl_gene_id":"ENSG00000252597.1","gene_symbol":"RNU7-137P","gene_name":"RNA, U7 small nuclear 137 pseudogene [Source:HGNC Symbol;Acc:HGNC:45671]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480821","summary":null,"start":18095571,"end":18095632,"strand":-1,"description":"RNA, U7 small nuclear 137 pseudogene [Source:HGNC Symbol;Acc:HGNC:45671]"}, {"versioned_ensembl_gene_id":"ENSG00000240302.3","gene_symbol":"RN7SL717P","gene_name":"RNA, 7SL, cytoplasmic 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:46733]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481118","summary":null,"start":199901081,"end":199901377,"strand":-1,"description":"RNA, 7SL, cytoplasmic 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:46733]"}, {"versioned_ensembl_gene_id":"ENSG00000202283.1","gene_symbol":"SNORA33","gene_name":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]","synonyms":"ACA33","biotype":"snoRNA","ncbi_id":"594839","summary":null,"start":103583135,"end":103583268,"strand":1,"description":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]"}, {"versioned_ensembl_gene_id":"ENSG00000199570.1","gene_symbol":"RNU6-228P","gene_name":"RNA, U6 small nuclear 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:47191]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479668","summary":null,"start":14352320,"end":14352425,"strand":1,"description":"RNA, U6 small nuclear 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:47191]"}, {"versioned_ensembl_gene_id":"ENSG00000207174.1","gene_symbol":"SNORD116-15","gene_name":"small nucleolar RNA, C/D box 116-15 [Source:HGNC Symbol;Acc:HGNC:33081]","synonyms":"HBII-85-15","biotype":"snoRNA","ncbi_id":"100033427","summary":null,"start":25081287,"end":25081378,"strand":1,"description":"small nucleolar RNA, C/D box 116-15 [Source:HGNC Symbol;Acc:HGNC:33081]"}, {"versioned_ensembl_gene_id":"ENSG00000200168.1","gene_symbol":"RNA5SP350","gene_name":"RNA, 5S ribosomal pseudogene 350 [Source:HGNC Symbol;Acc:HGNC:43250]","synonyms":"RN5S350","biotype":"rRNA","ncbi_id":"106481794","summary":null,"start":111040098,"end":111040208,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 350 [Source:HGNC Symbol;Acc:HGNC:43250]"}, {"versioned_ensembl_gene_id":"ENSG00000277613.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":90796,"end":90899,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201931.1","gene_symbol":"RNA5SP172","gene_name":"RNA, 5S ribosomal pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:43072]","synonyms":"RN5S172","biotype":"rRNA","ncbi_id":"106478997","summary":null,"start":177457111,"end":177457228,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:43072]"}, {"versioned_ensembl_gene_id":"ENSG00000283238.1","gene_symbol":"MIR1245B","gene_name":"microRNA 1245b [Source:HGNC Symbol;Acc:HGNC:41794]","synonyms":"hsa-mir-1245b","biotype":"miRNA","ncbi_id":"100616324","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188978093,"end":188978161,"strand":-1,"description":"microRNA 1245b [Source:HGNC Symbol;Acc:HGNC:41794]"}, {"versioned_ensembl_gene_id":"ENSG00000207713.3","gene_symbol":"MIR200C","gene_name":"microRNA 200c [Source:HGNC Symbol;Acc:HGNC:31580]","synonyms":"MIRN200C,hsa-mir-200c","biotype":"miRNA","ncbi_id":"406985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6963699,"end":6963766,"strand":1,"description":"microRNA 200c [Source:HGNC Symbol;Acc:HGNC:31580]"}, {"versioned_ensembl_gene_id":"ENSG00000278573.1","gene_symbol":"AC007325.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":59711,"end":60316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222338.1","gene_symbol":"RNU6-174P","gene_name":"RNA, U6 small nuclear 174, pseudogene [Source:HGNC Symbol;Acc:HGNC:47137]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481231","summary":null,"start":3726222,"end":3726327,"strand":-1,"description":"RNA, U6 small nuclear 174, pseudogene [Source:HGNC Symbol;Acc:HGNC:47137]"}, {"versioned_ensembl_gene_id":"ENSG00000200388.1","gene_symbol":"RNU6-618P","gene_name":"RNA, U6 small nuclear 618, pseudogene [Source:HGNC Symbol;Acc:HGNC:47581]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481376","summary":null,"start":31396390,"end":31396501,"strand":1,"description":"RNA, U6 small nuclear 618, pseudogene [Source:HGNC Symbol;Acc:HGNC:47581]"}, {"versioned_ensembl_gene_id":"ENSG00000212265.1","gene_symbol":"RNA5SP185","gene_name":"RNA, 5S ribosomal pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:43085]","synonyms":"RN5S185","biotype":"rRNA","ncbi_id":"100873447","summary":null,"start":56260333,"end":56260446,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 185 [Source:HGNC Symbol;Acc:HGNC:43085]"}, {"versioned_ensembl_gene_id":"ENSG00000252086.1","gene_symbol":"RNA5SP76","gene_name":"RNA, 5S ribosomal pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:42853]","synonyms":"RN5S76","biotype":"rRNA","ncbi_id":"100873310","summary":null,"start":219761789,"end":219761875,"strand":1,"description":"RNA, 5S ribosomal pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:42853]"}, {"versioned_ensembl_gene_id":"ENSG00000207131.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87826173,"end":87826285,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223208.1","gene_symbol":"RNU6-1217P","gene_name":"RNA, U6 small nuclear 1217, pseudogene [Source:HGNC Symbol;Acc:HGNC:48180]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481564","summary":null,"start":119434005,"end":119434108,"strand":-1,"description":"RNA, U6 small nuclear 1217, pseudogene [Source:HGNC Symbol;Acc:HGNC:48180]"}, {"versioned_ensembl_gene_id":"ENSG00000207206.1","gene_symbol":"RNU6-1035P","gene_name":"RNA, U6 small nuclear 1035, pseudogene [Source:HGNC Symbol;Acc:HGNC:47998]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481507","summary":null,"start":81725243,"end":81725349,"strand":-1,"description":"RNA, U6 small nuclear 1035, pseudogene [Source:HGNC Symbol;Acc:HGNC:47998]"}, {"versioned_ensembl_gene_id":"ENSG00000240584.3","gene_symbol":"RN7SL547P","gene_name":"RNA, 7SL, cytoplasmic 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:46563]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479421","summary":null,"start":7633562,"end":7633851,"strand":-1,"description":"RNA, 7SL, cytoplasmic 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:46563]"}, {"versioned_ensembl_gene_id":"ENSG00000265820.1","gene_symbol":"MIR3177","gene_name":"microRNA 3177 [Source:HGNC Symbol;Acc:HGNC:38364]","synonyms":"hsa-mir-3177","biotype":"miRNA","ncbi_id":"100423012","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1734985,"end":1735066,"strand":1,"description":"microRNA 3177 [Source:HGNC Symbol;Acc:HGNC:38364]"}, {"versioned_ensembl_gene_id":"ENSG00000221801.1","gene_symbol":"MIR548H2","gene_name":"microRNA 548h-2 [Source:HGNC Symbol;Acc:HGNC:35343]","synonyms":"MIRN548H2,hsa-mir-548h-2","biotype":"miRNA","ncbi_id":"100313773","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11306440,"end":11306527,"strand":-1,"description":"microRNA 548h-2 [Source:HGNC Symbol;Acc:HGNC:35343]"}, {"versioned_ensembl_gene_id":"ENSG00000252167.1","gene_symbol":"RNA5SP287","gene_name":"RNA, 5S ribosomal pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:43187]","synonyms":"RN5S287","biotype":"rRNA","ncbi_id":"100873540","summary":null,"start":81885496,"end":81885598,"strand":1,"description":"RNA, 5S ribosomal pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:43187]"}, {"versioned_ensembl_gene_id":"ENSG00000252277.1","gene_symbol":"SNORD116-30","gene_name":"small nucleolar RNA, C/D box 116-30 [Source:HGNC Symbol;Acc:HGNC:42797]","synonyms":"HBII-85-30","biotype":"snoRNA","ncbi_id":"100873856","summary":null,"start":25108268,"end":25108352,"strand":1,"description":"small nucleolar RNA, C/D box 116-30 [Source:HGNC Symbol;Acc:HGNC:42797]"}, {"versioned_ensembl_gene_id":"ENSG00000263941.2","gene_symbol":"RN7SL32P","gene_name":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480930","summary":null,"start":233205199,"end":233205479,"strand":1,"description":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]"}, {"versioned_ensembl_gene_id":"ENSG00000266423.1","gene_symbol":"MIR3163","gene_name":"microRNA 3163 [Source:HGNC Symbol;Acc:HGNC:38209]","synonyms":"hsa-mir-3163","biotype":"miRNA","ncbi_id":"100423029","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66934434,"end":66934506,"strand":-1,"description":"microRNA 3163 [Source:HGNC Symbol;Acc:HGNC:38209]"}, {"versioned_ensembl_gene_id":"ENSG00000222248.1","gene_symbol":"RNA5SP201","gene_name":"RNA, 5S ribosomal pseudogene 201 [Source:HGNC Symbol;Acc:HGNC:43101]","synonyms":"RN5S201","biotype":"rRNA","ncbi_id":"100873462","summary":null,"start":3088686,"end":3088809,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 201 [Source:HGNC Symbol;Acc:HGNC:43101]"}, {"versioned_ensembl_gene_id":"ENSG00000276323.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,amida,FB1,FB1,INO80F,INO80F","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000251958.1","gene_symbol":"RNU6-1102P","gene_name":"RNA, U6 small nuclear 1102, pseudogene 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[Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202014.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48153434,"end":48153535,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207003.1","gene_symbol":"RNU6-611P","gene_name":"RNA, U6 small nuclear 611, pseudogene [Source:HGNC Symbol;Acc:HGNC:47574]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479836","summary":null,"start":45047458,"end":45047561,"strand":1,"description":"RNA, U6 small nuclear 611, pseudogene [Source:HGNC Symbol;Acc:HGNC:47574]"}, {"versioned_ensembl_gene_id":"ENSG00000266569.2","gene_symbol":"RN7SL377P","gene_name":"RNA, 7SL, cytoplasmic 377, pseudogene [Source:HGNC Symbol;Acc:HGNC:46393]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479360","summary":null,"start":72822894,"end":72823171,"strand":-1,"description":"RNA, 7SL, cytoplasmic 377, 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{"versioned_ensembl_gene_id":"ENSG00000200759.1","gene_symbol":"RNU6-884P","gene_name":"RNA, U6 small nuclear 884, pseudogene [Source:HGNC Symbol;Acc:HGNC:47847]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479957","summary":null,"start":151022746,"end":151022852,"strand":-1,"description":"RNA, U6 small nuclear 884, pseudogene [Source:HGNC Symbol;Acc:HGNC:47847]"}, {"versioned_ensembl_gene_id":"ENSG00000277551.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54913656,"end":54913762,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000243352.3","gene_symbol":"RN7SL8P","gene_name":"RNA, 7SL, cytoplasmic 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:10043]","synonyms":"RN7SLP5,RN7SL433P,7L63","biotype":"misc_RNA","ncbi_id":"6034","summary":null,"start":104911928,"end":104912193,"strand":1,"description":"RNA, 7SL, 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147272335,"end":147272408,"strand":-1,"description":"microRNA 510 [Source:HGNC Symbol;Acc:HGNC:32147]"}, {"versioned_ensembl_gene_id":"ENSG00000206693.1","gene_symbol":"SNORA56","gene_name":"small nucleolar RNA, H/ACA box 56 [Source:HGNC Symbol;Acc:HGNC:32650]","synonyms":"ACA56","biotype":"snoRNA","ncbi_id":"677835","summary":"Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009]","start":154774998,"end":154775126,"strand":1,"description":"small nucleolar RNA, H/ACA box 56 [Source:HGNC Symbol;Acc:HGNC:32650]"}, {"versioned_ensembl_gene_id":"ENSG00000234353.2","gene_symbol":"AP000346.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23638492,"end":23640762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267195.1","gene_symbol":"MIR212","gene_name":"microRNA 212 [Source:HGNC Symbol;Acc:HGNC:31589]","synonyms":"MIRN212,hsa-mir-212","biotype":"miRNA","ncbi_id":"406994","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2050271,"end":2050380,"strand":-1,"description":"microRNA 212 [Source:HGNC Symbol;Acc:HGNC:31589]"}, {"versioned_ensembl_gene_id":"ENSG00000207996.1","gene_symbol":"MIR301A","gene_name":"microRNA 301a [Source:HGNC Symbol;Acc:HGNC:31622]","synonyms":"MIRN301A,MIRN301,hsa-mir-301a,hsa-mir-301","biotype":"miRNA","ncbi_id":"407027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59151136,"end":59151221,"strand":-1,"description":"microRNA 301a [Source:HGNC Symbol;Acc:HGNC:31622]"}, {"versioned_ensembl_gene_id":"ENSG00000252397.1","gene_symbol":"RNU5A-4P","gene_name":"RNA, U5A small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42521]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873870","summary":null,"start":33829539,"end":33829649,"strand":-1,"description":"RNA, U5A small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42521]"}, {"versioned_ensembl_gene_id":"ENSG00000207468.1","gene_symbol":"SNORA19","gene_name":"small nucleolar RNA, H/ACA box 19 [Source:HGNC Symbol;Acc:HGNC:32609]","synonyms":"ACA19","biotype":"snoRNA","ncbi_id":"641451","summary":null,"start":119060011,"end":119060138,"strand":-1,"description":"small nucleolar RNA, H/ACA box 19 [Source:HGNC Symbol;Acc:HGNC:32609]"}, {"versioned_ensembl_gene_id":"ENSG00000244532.1","gene_symbol":"RN7SL380P","gene_name":"RNA, 7SL, cytoplasmic 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:46396]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479361","summary":null,"start":6783854,"end":6784161,"strand":-1,"description":"RNA, 7SL, cytoplasmic 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:46396]"}, {"versioned_ensembl_gene_id":"ENSG00000252983.1","gene_symbol":"RNU7-35P","gene_name":"RNA, U7 small nuclear 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:34131]","synonyms":"U7.35","biotype":"snRNA","ncbi_id":"100147822","summary":null,"start":43194421,"end":43194482,"strand":1,"description":"RNA, U7 small nuclear 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:34131]"}, {"versioned_ensembl_gene_id":"ENSG00000220986.1","gene_symbol":"SNORA50D","gene_name":"small nucleolar RNA, H/ACA box 50D [Source:HGNC Symbol;Acc:HGNC:50433]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616958","summary":null,"start":69160806,"end":69160939,"strand":1,"description":"small nucleolar RNA, H/ACA box 50D [Source:HGNC Symbol;Acc:HGNC:50433]"}, {"versioned_ensembl_gene_id":"ENSG00000253059.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":35756327,"end":35756463,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000284197.1","gene_symbol":"MIR658","gene_name":"microRNA 658 [Source:HGNC Symbol;Acc:HGNC:32914]","synonyms":"hsa-mir-658,MIRN658","biotype":"miRNA","ncbi_id":"724028","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37844272,"end":37844371,"strand":-1,"description":"microRNA 658 [Source:HGNC Symbol;Acc:HGNC:32914]"}, {"versioned_ensembl_gene_id":"ENSG00000207654.4","gene_symbol":"MIR128-1","gene_name":"microRNA 128-1 [Source:HGNC Symbol;Acc:HGNC:31510]","synonyms":"MIRN128A,MIRN128-1,hsa-mir-128a,hsa-mir-128-1","biotype":"miRNA","ncbi_id":"406915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":135665397,"end":135665478,"strand":1,"description":"microRNA 128-1 [Source:HGNC Symbol;Acc:HGNC:31510]"}, {"versioned_ensembl_gene_id":"ENSG00000278818.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55285227,"end":55285558,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212229.1","gene_symbol":"SNORD65","gene_name":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]","synonyms":"SNORD65A,HBII-135","biotype":"snoRNA","ncbi_id":"692106","summary":null,"start":67210408,"end":67210480,"strand":-1,"description":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]"}, {"versioned_ensembl_gene_id":"ENSG00000277698.1","gene_symbol":"MIR6770-2","gene_name":"microRNA 6770-2 [Source:HGNC Symbol;Acc:HGNC:50115]","synonyms":"hsa-mir-6770-2","biotype":"miRNA","ncbi_id":"102465908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16329305,"end":16329364,"strand":1,"description":"microRNA 6770-2 [Source:HGNC Symbol;Acc:HGNC:50115]"}, {"versioned_ensembl_gene_id":"ENSG00000202275.1","gene_symbol":"SNORD51","gene_name":"Small nucleolar RNA SNORD51 [Source:RFAM;Acc:RF00280]","synonyms":"U51,RNU51","biotype":"snoRNA","ncbi_id":"26798","summary":null,"start":103797272,"end":103797348,"strand":-1,"description":"Small nucleolar RNA SNORD51 [Source:RFAM;Acc:RF00280]"}, {"versioned_ensembl_gene_id":"ENSG00000274953.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000283705.1","gene_symbol":"MIR92A1","gene_name":"microRNA 92a-1 [Source:HGNC Symbol;Acc:HGNC:31643]","synonyms":"MIRN92A1,MIRN92-1,hsa-mir-92a-1,hsa-mir-92-1","biotype":"miRNA","ncbi_id":"407048","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91351314,"end":91351391,"strand":1,"description":"microRNA 92a-1 [Source:HGNC Symbol;Acc:HGNC:31643]"}, {"versioned_ensembl_gene_id":"ENSG00000206697.1","gene_symbol":"RNY1P8","gene_name":"RNA, Ro-associated Y1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42485]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873807","summary":null,"start":73227147,"end":73227260,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42485]"}, {"versioned_ensembl_gene_id":"ENSG00000200530.1","gene_symbol":"SNORD35B","gene_name":"small nucleolar RNA, C/D box 35B [Source:HGNC Symbol;Acc:HGNC:17365]","synonyms":"U35B,RNU35B","biotype":"snoRNA","ncbi_id":"84546","summary":null,"start":49497720,"end":49497806,"strand":1,"description":"small nucleolar RNA, C/D box 35B [Source:HGNC Symbol;Acc:HGNC:17365]"}, {"versioned_ensembl_gene_id":"ENSG00000212100.2","gene_symbol":"MIR764","gene_name":"microRNA 764 [Source:HGNC Symbol;Acc:HGNC:37306]","synonyms":"hsa-mir-764","biotype":"miRNA","ncbi_id":"100313838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114639435,"end":114639519,"strand":1,"description":"microRNA 764 [Source:HGNC Symbol;Acc:HGNC:37306]"}, {"versioned_ensembl_gene_id":"ENSG00000206609.1","gene_symbol":"SNORD116-11","gene_name":"small nucleolar RNA, C/D box 116-11 [Source:HGNC Symbol;Acc:HGNC:33077]","synonyms":"HBII-85-11","biotype":"snoRNA","ncbi_id":"100033423","summary":null,"start":25075929,"end":25076020,"strand":1,"description":"small nucleolar RNA, C/D box 116-11 [Source:HGNC Symbol;Acc:HGNC:33077]"}, {"versioned_ensembl_gene_id":"ENSG00000199664.1","gene_symbol":"RNU6-1266P","gene_name":"RNA, U6 small nuclear 1266, pseudogene [Source:HGNC Symbol;Acc:HGNC:48229]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480118","summary":null,"start":77776951,"end":77777055,"strand":-1,"description":"RNA, U6 small nuclear 1266, pseudogene [Source:HGNC Symbol;Acc:HGNC:48229]"}, {"versioned_ensembl_gene_id":"ENSG00000201744.1","gene_symbol":"RNU6-34P","gene_name":"RNA, U6 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:34278]","synonyms":"RNU6-34","biotype":"snRNA","ncbi_id":"100873749","summary":null,"start":96152297,"end":96152403,"strand":-1,"description":"RNA, U6 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:34278]"}, {"versioned_ensembl_gene_id":"ENSG00000212329.1","gene_symbol":"RNU6-316P","gene_name":"RNA, U6 small nuclear 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:47279]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481279","summary":null,"start":14190700,"end":14190806,"strand":1,"description":"RNA, U6 small nuclear 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:47279]"}, {"versioned_ensembl_gene_id":"ENSG00000201644.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75662120,"end":75662213,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278261.1","gene_symbol":"SNORD1A","gene_name":"small nucleolar RNA, C/D box 1A [Source:HGNC Symbol;Acc:HGNC:32556]","synonyms":"snR38A,R38A","biotype":"snoRNA","ncbi_id":"677848","summary":null,"start":76561634,"end":76561705,"strand":1,"description":"small nucleolar RNA, C/D box 1A [Source:HGNC Symbol;Acc:HGNC:32556]"}, {"versioned_ensembl_gene_id":"ENSG00000212580.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":49888868,"end":49888986,"strand":-1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000241175.3","gene_symbol":"RN7SL494P","gene_name":"RNA, 7SL, cytoplasmic 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:46510]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481057","summary":null,"start":50244628,"end":50244931,"strand":-1,"description":"RNA, 7SL, cytoplasmic 494, pseudogene [Source:HGNC Symbol;Acc:HGNC:46510]"}, {"versioned_ensembl_gene_id":"ENSG00000273932.1","gene_symbol":"MIR6877","gene_name":"microRNA 6877 [Source:HGNC Symbol;Acc:HGNC:50205]","synonyms":"hsa-mir-6877","biotype":"miRNA","ncbi_id":"102465528","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133051996,"end":133052059,"strand":1,"description":"microRNA 6877 [Source:HGNC Symbol;Acc:HGNC:50205]"}, {"versioned_ensembl_gene_id":"ENSG00000266035.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32036120,"end":32036240,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222874.1","gene_symbol":"RN7SKP33","gene_name":"RNA, 7SK small nuclear pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45757]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480843","summary":null,"start":46859333,"end":46859672,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45757]"}, {"versioned_ensembl_gene_id":"ENSG00000251752.1","gene_symbol":"RNU4-29P","gene_name":"RNA, U4 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:46965]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481181","summary":null,"start":83275941,"end":83276114,"strand":1,"description":"RNA, U4 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:46965]"}, {"versioned_ensembl_gene_id":"ENSG00000252953.1","gene_symbol":"RNU6-232P","gene_name":"RNA, U6 small nuclear 232, pseudogene [Source:HGNC Symbol;Acc:HGNC:47195]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480388","summary":null,"start":125388934,"end":125388997,"strand":1,"description":"RNA, U6 small nuclear 232, pseudogene [Source:HGNC Symbol;Acc:HGNC:47195]"}, {"versioned_ensembl_gene_id":"ENSG00000200393.1","gene_symbol":"RNU6-698P","gene_name":"RNA, U6 small nuclear 698, pseudogene [Source:HGNC Symbol;Acc:HGNC:47661]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481401","summary":null,"start":53653685,"end":53653791,"strand":1,"description":"RNA, U6 small nuclear 698, pseudogene [Source:HGNC Symbol;Acc:HGNC:47661]"}, {"versioned_ensembl_gene_id":"ENSG00000275222.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8998849,"end":8999100,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222971.1","gene_symbol":"RNA5SP222","gene_name":"RNA, 5S ribosomal pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:43122]","synonyms":"RN5S222","biotype":"rRNA","ncbi_id":"100873481","summary":null,"start":146340420,"end":146340524,"strand":1,"description":"RNA, 5S ribosomal pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:43122]"}, {"versioned_ensembl_gene_id":"ENSG00000277295.1","gene_symbol":"RN7SL489P","gene_name":"RNA, 7SL, cytoplasmic 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:46505]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481056","summary":null,"start":75268430,"end":75268652,"strand":1,"description":"RNA, 7SL, cytoplasmic 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:46505]"}, {"versioned_ensembl_gene_id":"ENSG00000251841.1","gene_symbol":"RNU6-1334P","gene_name":"RNA, U6 small nuclear 1334, pseudogene [Source:HGNC Symbol;Acc:HGNC:48297]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480148","summary":null,"start":2784749,"end":2784853,"strand":1,"description":"RNA, U6 small nuclear 1334, pseudogene [Source:HGNC Symbol;Acc:HGNC:48297]"}, {"versioned_ensembl_gene_id":"ENSG00000207227.1","gene_symbol":"RNU6-900P","gene_name":"RNA, U6 small nuclear 900, pseudogene [Source:HGNC Symbol;Acc:HGNC:47863]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481463","summary":null,"start":37891347,"end":37891448,"strand":1,"description":"RNA, U6 small nuclear 900, pseudogene [Source:HGNC Symbol;Acc:HGNC:47863]"}, {"versioned_ensembl_gene_id":"ENSG00000207222.1","gene_symbol":"RNU6-456P","gene_name":"RNA, U6 small nuclear 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:47419]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481323","summary":null,"start":134500178,"end":134500284,"strand":-1,"description":"RNA, U6 small nuclear 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:47419]"}, {"versioned_ensembl_gene_id":"ENSG00000263755.2","gene_symbol":"RN7SL498P","gene_name":"RNA, 7SL, cytoplasmic 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:46514]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479405","summary":null,"start":6001733,"end":6002030,"strand":1,"description":"RNA, 7SL, cytoplasmic 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:46514]"}, {"versioned_ensembl_gene_id":"ENSG00000264349.1","gene_symbol":"MIR4258","gene_name":"microRNA 4258 [Source:HGNC Symbol;Acc:HGNC:38281]","synonyms":"hsa-mir-4258","biotype":"miRNA","ncbi_id":"100423020","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154975693,"end":154975783,"strand":1,"description":"microRNA 4258 [Source:HGNC Symbol;Acc:HGNC:38281]"}, {"versioned_ensembl_gene_id":"ENSG00000221059.1","gene_symbol":"RNU6ATAC6P","gene_name":"RNA, U6atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46905]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479545","summary":null,"start":87910220,"end":87910345,"strand":1,"description":"RNA, U6atac small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:46905]"}, {"versioned_ensembl_gene_id":"ENSG00000252243.1","gene_symbol":"RNU6-412P","gene_name":"RNA, U6 small nuclear 412, pseudogene [Source:HGNC Symbol;Acc:HGNC:47375]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481308","summary":null,"start":46531237,"end":46531342,"strand":-1,"description":"RNA, U6 small nuclear 412, pseudogene [Source:HGNC Symbol;Acc:HGNC:47375]"}, {"versioned_ensembl_gene_id":"ENSG00000251997.1","gene_symbol":"RNA5SP458","gene_name":"RNA, 5S ribosomal pseudogene 458 [Source:HGNC Symbol;Acc:HGNC:43358]","synonyms":"RN5S458","biotype":"rRNA","ncbi_id":"106479016","summary":null,"start":50319002,"end":50319120,"strand":1,"description":"RNA, 5S ribosomal pseudogene 458 [Source:HGNC Symbol;Acc:HGNC:43358]"}, {"versioned_ensembl_gene_id":"ENSG00000200648.1","gene_symbol":"RNU6-226P","gene_name":"RNA, U6 small nuclear 226, pseudogene [Source:HGNC Symbol;Acc:HGNC:47189]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481249","summary":null,"start":175703898,"end":175704004,"strand":1,"description":"RNA, U6 small nuclear 226, pseudogene [Source:HGNC Symbol;Acc:HGNC:47189]"}, {"versioned_ensembl_gene_id":"ENSG00000263881.1","gene_symbol":"MIR4436B2","gene_name":"microRNA 4436b-2 [Source:HGNC Symbol;Acc:HGNC:43451]","synonyms":"hsa-mir-4436b-2","biotype":"miRNA","ncbi_id":"100847033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110284853,"end":110284943,"strand":1,"description":"microRNA 4436b-2 [Source:HGNC Symbol;Acc:HGNC:43451]"}, {"versioned_ensembl_gene_id":"ENSG00000252334.1","gene_symbol":"RNU6-1337P","gene_name":"RNA, U6 small nuclear 1337, pseudogene [Source:HGNC Symbol;Acc:HGNC:48300]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481602","summary":null,"start":58483749,"end":58483843,"strand":-1,"description":"RNA, U6 small nuclear 1337, pseudogene [Source:HGNC Symbol;Acc:HGNC:48300]"}, {"versioned_ensembl_gene_id":"ENSG00000263527.1","gene_symbol":"MIR4526","gene_name":"microRNA 4526 [Source:HGNC Symbol;Acc:HGNC:41618]","synonyms":"hsa-mir-4526","biotype":"miRNA","ncbi_id":"100616130","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13611114,"end":13611200,"strand":1,"description":"microRNA 4526 [Source:HGNC Symbol;Acc:HGNC:41618]"}, {"versioned_ensembl_gene_id":"ENSG00000207599.1","gene_symbol":"MIR520E","gene_name":"microRNA 520e [Source:HGNC Symbol;Acc:HGNC:32093]","synonyms":"MIRN520E,hsa-mir-520e","biotype":"miRNA","ncbi_id":"574461","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53675711,"end":53675797,"strand":1,"description":"microRNA 520e [Source:HGNC Symbol;Acc:HGNC:32093]"}, {"versioned_ensembl_gene_id":"ENSG00000119950.20","gene_symbol":"MXI1","gene_name":"MAX interactor 1, dimerization protein [Source:HGNC Symbol;Acc:HGNC:7534]","synonyms":"MXI,MXD2,MAD2,bHLHc11","biotype":"protein_coding","ncbi_id":"4601","summary":"Expression of the c-myc gene, which produces an oncogenic transcription factor, is tightly regulated in normal cells but is frequently deregulated in human cancers. The protein encoded by this gene is a transcriptional repressor thought to negatively regulate MYC function, and is therefore a potential tumor suppressor. This protein inhibits the transcriptional activity of MYC by competing for MAX, another basic helix-loop-helix protein that binds to MYC and is required for its function. Defects in this gene are frequently found in patients with prostate tumors. Three alternatively spliced transcripts encoding different isoforms have been described. Additional alternatively spliced transcripts may exist but the products of these transcripts have not been verified experimentally. [provided by RefSeq, Jul 2008]","start":110207605,"end":110287365,"strand":1,"description":"MAX interactor 1, dimerization protein [Source:HGNC Symbol;Acc:HGNC:7534]"}, {"versioned_ensembl_gene_id":"ENSG00000275101.1","gene_symbol":"MIR6766","gene_name":"microRNA 6766 [Source:HGNC Symbol;Acc:HGNC:49941]","synonyms":"hsa-mir-6766","biotype":"miRNA","ncbi_id":"102466983","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89326739,"end":89326810,"strand":-1,"description":"microRNA 6766 [Source:HGNC Symbol;Acc:HGNC:49941]"}, {"versioned_ensembl_gene_id":"ENSG00000199781.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":232828653,"end":232828751,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284204.1","gene_symbol":"MIR19A","gene_name":"microRNA 19a [Source:HGNC Symbol;Acc:HGNC:31574]","synonyms":"hsa-mir-19a,MIRN19A","biotype":"miRNA","ncbi_id":"406979","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91350891,"end":91350972,"strand":1,"description":"microRNA 19a [Source:HGNC Symbol;Acc:HGNC:31574]"}, {"versioned_ensembl_gene_id":"ENSG00000211581.1","gene_symbol":"MIR765","gene_name":"microRNA 765 [Source:HGNC Symbol;Acc:HGNC:33141]","synonyms":"MIRN765,hsa-mir-765","biotype":"miRNA","ncbi_id":"768220","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":156936131,"end":156936244,"strand":-1,"description":"microRNA 765 [Source:HGNC Symbol;Acc:HGNC:33141]"}, {"versioned_ensembl_gene_id":"ENSG00000207306.1","gene_symbol":"RNU6-1152P","gene_name":"RNA, U6 small nuclear 1152, pseudogene [Source:HGNC Symbol;Acc:HGNC:48115]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480073","summary":null,"start":48196680,"end":48196786,"strand":-1,"description":"RNA, U6 small nuclear 1152, pseudogene [Source:HGNC Symbol;Acc:HGNC:48115]"}, {"versioned_ensembl_gene_id":"ENSG00000200261.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112169286,"end":112169397,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274170.1","gene_symbol":"RFPL3-AS1_2","gene_name":"RFPL3 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02172]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32368497,"end":32368567,"strand":1,"description":"RFPL3 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02172]"}, {"versioned_ensembl_gene_id":"ENSG00000263968.2","gene_symbol":"RN7SL381P","gene_name":"RNA, 7SL, cytoplasmic 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:46397]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479362","summary":null,"start":85659378,"end":85659675,"strand":1,"description":"RNA, 7SL, cytoplasmic 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:46397]"}, {"versioned_ensembl_gene_id":"ENSG00000252255.1","gene_symbol":"RNU2-35P","gene_name":"RNA, U2 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48528]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480212","summary":null,"start":125649746,"end":125649887,"strand":1,"description":"RNA, U2 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48528]"}, {"versioned_ensembl_gene_id":"ENSG00000281707.1","gene_symbol":"AC099669.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44528955,"end":44529391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244218.3","gene_symbol":"RN7SL81P","gene_name":"RNA, 7SL, cytoplasmic 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:46097]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479253","summary":null,"start":128761338,"end":128761598,"strand":1,"description":"RNA, 7SL, cytoplasmic 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:46097]"}, {"versioned_ensembl_gene_id":"ENSG00000278519.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000260682.3","gene_symbol":"RN7SKP176","gene_name":"RNA, 7SK small nuclear pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:45900]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106635536","summary":null,"start":81961926,"end":81962243,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:45900]"}, {"versioned_ensembl_gene_id":"ENSG00000201816.1","gene_symbol":"SNORA73","gene_name":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56079394,"end":56079594,"strand":-1,"description":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]"}, {"versioned_ensembl_gene_id":"ENSG00000199378.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100021804,"end":100021906,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207317.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140019492,"end":140019592,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222544.1","gene_symbol":"RNU6-735P","gene_name":"RNA, U6 small nuclear 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:47698]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481412","summary":null,"start":95438737,"end":95438843,"strand":-1,"description":"RNA, U6 small nuclear 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:47698]"}, {"versioned_ensembl_gene_id":"ENSG00000207121.1","gene_symbol":"RNU6-1230P","gene_name":"RNA, U6 small nuclear 1230, pseudogene [Source:HGNC Symbol;Acc:HGNC:48193]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481944","summary":null,"start":149934376,"end":149934483,"strand":1,"description":"RNA, U6 small nuclear 1230, pseudogene [Source:HGNC Symbol;Acc:HGNC:48193]"}, {"versioned_ensembl_gene_id":"ENSG00000238561.1","gene_symbol":"RNU6ATAC28P","gene_name":"RNA, U6atac small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46927]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479555","summary":null,"start":83750384,"end":83750501,"strand":1,"description":"RNA, U6atac small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46927]"}, {"versioned_ensembl_gene_id":"ENSG00000265633.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30942815,"end":30943117,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000267169.1","gene_symbol":"AC022098.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14137179,"end":14171267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215217.6","gene_symbol":"C5orf49","gene_name":"chromosome 5 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:27028]","synonyms":"LOC134121","biotype":"protein_coding","ncbi_id":"134121","summary":null,"start":7830378,"end":7851490,"strand":-1,"description":"chromosome 5 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:27028]"}, {"versioned_ensembl_gene_id":"ENSG00000262815.1","gene_symbol":"AC087501.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9464742,"end":9467422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264974.1","gene_symbol":"MIR4789","gene_name":"microRNA 4789 [Source:HGNC Symbol;Acc:HGNC:41719]","synonyms":"hsa-mir-4789","biotype":"miRNA","ncbi_id":"100616395","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":175369540,"end":175369621,"strand":1,"description":"microRNA 4789 [Source:HGNC Symbol;Acc:HGNC:41719]"}, {"versioned_ensembl_gene_id":"ENSG00000200486.1","gene_symbol":"SNORD115-11","gene_name":"small nucleolar RNA, C/D box 115-11 [Source:HGNC Symbol;Acc:HGNC:33030]","synonyms":"HBII-52-11","biotype":"snoRNA","ncbi_id":"100033448","summary":null,"start":25189414,"end":25189495,"strand":1,"description":"small nucleolar RNA, C/D box 115-11 [Source:HGNC Symbol;Acc:HGNC:33030]"}, {"versioned_ensembl_gene_id":"ENSG00000252556.1","gene_symbol":"RNU6-256P","gene_name":"RNA, U6 small nuclear 256, pseudogene [Source:HGNC Symbol;Acc:HGNC:47219]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479680","summary":null,"start":122004355,"end":122004451,"strand":1,"description":"RNA, U6 small nuclear 256, pseudogene [Source:HGNC Symbol;Acc:HGNC:47219]"}, {"versioned_ensembl_gene_id":"ENSG00000200706.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":38207274,"end":38207345,"strand":1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000252856.1","gene_symbol":"RNA5SP503","gene_name":"RNA, 5S ribosomal pseudogene 503 [Source:HGNC Symbol;Acc:HGNC:43403]","synonyms":"RN5S503","biotype":"rRNA","ncbi_id":"100873554","summary":null,"start":48206258,"end":48206374,"strand":1,"description":"RNA, 5S ribosomal pseudogene 503 [Source:HGNC Symbol;Acc:HGNC:43403]"}, {"versioned_ensembl_gene_id":"ENSG00000207930.1","gene_symbol":"MIR603","gene_name":"microRNA 603 [Source:HGNC Symbol;Acc:HGNC:32859]","synonyms":"MIRN603,hsa-mir-603","biotype":"miRNA","ncbi_id":"693188","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24275685,"end":24275781,"strand":1,"description":"microRNA 603 [Source:HGNC Symbol;Acc:HGNC:32859]"}, {"versioned_ensembl_gene_id":"ENSG00000252082.1","gene_symbol":"RNU6-547P","gene_name":"RNA, U6 small nuclear 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:47510]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481902","summary":null,"start":172703124,"end":172703225,"strand":1,"description":"RNA, U6 small nuclear 547, pseudogene [Source:HGNC Symbol;Acc:HGNC:47510]"}, {"versioned_ensembl_gene_id":"ENSG00000221125.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":49949316,"end":49949527,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000278764.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46266690,"end":46266971,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277668.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130603461,"end":130603724,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200407.1","gene_symbol":"RNU6-1169P","gene_name":"RNA, U6 small nuclear 1169, pseudogene [Source:HGNC Symbol;Acc:HGNC:48132]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480080","summary":null,"start":41448742,"end":41448844,"strand":-1,"description":"RNA, U6 small nuclear 1169, pseudogene [Source:HGNC Symbol;Acc:HGNC:48132]"}, {"versioned_ensembl_gene_id":"ENSG00000201135.1","gene_symbol":"RNU6-777P","gene_name":"RNA, U6 small nuclear 777, pseudogene [Source:HGNC Symbol;Acc:HGNC:47740]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481426","summary":null,"start":12077881,"end":12077984,"strand":-1,"description":"RNA, U6 small nuclear 777, pseudogene [Source:HGNC Symbol;Acc:HGNC:47740]"}, {"versioned_ensembl_gene_id":"ENSG00000201291.1","gene_symbol":"RNU1-34P","gene_name":"RNA, U1 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:48376]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481607","summary":null,"start":75473738,"end":75473894,"strand":-1,"description":"RNA, U1 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:48376]"}, {"versioned_ensembl_gene_id":"ENSG00000251917.1","gene_symbol":"RNU1-86P","gene_name":"RNA, U1 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:48428]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480666","summary":null,"start":23946618,"end":23946771,"strand":-1,"description":"RNA, U1 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:48428]"}, {"versioned_ensembl_gene_id":"ENSG00000281808.1","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":136726748,"end":136726879,"strand":-1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000252361.1","gene_symbol":"RNU6-118P","gene_name":"RNA, U6 small nuclear 118, pseudogene [Source:HGNC Symbol;Acc:HGNC:47081]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479618","summary":null,"start":62815966,"end":62816067,"strand":-1,"description":"RNA, U6 small nuclear 118, pseudogene [Source:HGNC Symbol;Acc:HGNC:47081]"}, {"versioned_ensembl_gene_id":"ENSG00000267723.1","gene_symbol":"AC011509.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14254189,"end":14293205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266913.1","gene_symbol":"LINC01841","gene_name":"long intergenic non-protein coding RNA 1841 [Source:HGNC Symbol;Acc:HGNC:52655]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372288","summary":null,"start":14305458,"end":14370196,"strand":-1,"description":"long intergenic non-protein coding RNA 1841 [Source:HGNC Symbol;Acc:HGNC:52655]"}, {"versioned_ensembl_gene_id":"ENSG00000267406.1","gene_symbol":"AC011509.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14267807,"end":14269377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262961.1","gene_symbol":"AC006236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5730289,"end":5731085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255919.1","gene_symbol":"AC226150.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133217210,"end":133217675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072071.16","gene_symbol":"ADGRL1","gene_name":"adhesion G protein-coupled receptor L1 [Source:HGNC Symbol;Acc:HGNC:20973]","synonyms":"LPHN1,LEC2,KIAA0821,CIRL1","biotype":"protein_coding","ncbi_id":"22859","summary":"This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/calcitonin family of GPCRs) being non-covalently bound at the cell membrane. Latrophilin-1 has been shown to recruit the neurotoxin from black widow spider venom, alpha-latrotoxin, to the synapse plasma membrane. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]","start":14147743,"end":14206187,"strand":-1,"description":"adhesion G protein-coupled receptor L1 [Source:HGNC Symbol;Acc:HGNC:20973]"}, {"versioned_ensembl_gene_id":"ENSG00000165799.4","gene_symbol":"RNASE7","gene_name":"ribonuclease A family member 7 [Source:HGNC Symbol;Acc:HGNC:19278]","synonyms":"RAE1","biotype":"protein_coding","ncbi_id":"84659","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family, a subset of the ribonuclease A superfamily. The protein has broad-spectrum antimicrobial activity against bacteria and fungi. [provided by RefSeq, Oct 2014]","start":21042226,"end":21044234,"strand":1,"description":"ribonuclease A family member 7 [Source:HGNC Symbol;Acc:HGNC:19278]"}, {"versioned_ensembl_gene_id":"ENSG00000258604.1","gene_symbol":"AL161668.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21024172,"end":21029271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255472.1","gene_symbol":"AL161668.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21032818,"end":21033895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232086.1","gene_symbol":"AL159990.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70708047,"end":70712863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265453.1","gene_symbol":"AC026254.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27281094,"end":27281415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049860.13","gene_symbol":"HEXB","gene_name":"hexosaminidase subunit beta [Source:HGNC Symbol;Acc:HGNC:4879]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3074","summary":"Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":74640023,"end":74722647,"strand":1,"description":"hexosaminidase subunit beta [Source:HGNC Symbol;Acc:HGNC:4879]"}, {"versioned_ensembl_gene_id":"ENSG00000257070.1","gene_symbol":"AP003170.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113769660,"end":113769994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256603.1","gene_symbol":"AP003170.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113770393,"end":113771691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243353.1","gene_symbol":"RPS29P19","gene_name":"ribosomal protein S29 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271383","summary":null,"start":113751116,"end":113751286,"strand":-1,"description":"ribosomal protein S29 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36118]"}, {"versioned_ensembl_gene_id":"ENSG00000133056.13","gene_symbol":"PIK3C2B","gene_name":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta [Source:HGNC Symbol;Acc:HGNC:8972]","synonyms":"PI3K-C2beta,C2-PI3K","biotype":"protein_coding","ncbi_id":"5287","summary":"The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. The PI3-kinase activity of this protein is sensitive to low nanomolar levels of the inhibitor wortmanin. The C2 domain of this protein was shown to bind phospholipids but not Ca2+, which suggests that this enzyme may function in a calcium-independent manner. [provided by RefSeq, Jul 2008]","start":204422628,"end":204494724,"strand":-1,"description":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta [Source:HGNC Symbol;Acc:HGNC:8972]"}, {"versioned_ensembl_gene_id":"ENSG00000251041.1","gene_symbol":"AC106732.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74321631,"end":74340152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250446.1","gene_symbol":"LINC01332","gene_name":"long intergenic non-protein coding RNA 1332 [Source:HGNC Symbol;Acc:HGNC:50540]","synonyms":"TCONS_00009701","biotype":"lincRNA","ncbi_id":"106144530","summary":null,"start":74327995,"end":74334766,"strand":-1,"description":"long intergenic non-protein coding RNA 1332 [Source:HGNC Symbol;Acc:HGNC:50540]"}, {"versioned_ensembl_gene_id":"ENSG00000248942.1","gene_symbol":"LINC01335","gene_name":"long intergenic non-protein coding RNA 1335 [Source:HGNC Symbol;Acc:HGNC:50542]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102503429","summary":null,"start":74306410,"end":74308325,"strand":-1,"description":"long intergenic non-protein coding RNA 1335 [Source:HGNC Symbol;Acc:HGNC:50542]"}, {"versioned_ensembl_gene_id":"ENSG00000265265.1","gene_symbol":"AC233702.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21519514,"end":21521269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254984.1","gene_symbol":"FTLP6","gene_name":"ferritin light chain pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37954]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462788","summary":null,"start":66771246,"end":66771667,"strand":-1,"description":"ferritin light chain pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37954]"}, {"versioned_ensembl_gene_id":"ENSG00000219133.2","gene_symbol":"AL592114.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204346776,"end":204347258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204706.14","gene_symbol":"MAMDC2-AS1","gene_name":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507244","summary":null,"start":70033921,"end":70175888,"strand":-1,"description":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]"}, {"versioned_ensembl_gene_id":"ENSG00000170498.8","gene_symbol":"KISS1","gene_name":"KiSS-1 metastasis-suppressor [Source:HGNC Symbol;Acc:HGNC:6341]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3814","summary":"This gene is a metastasis suppressor gene that suppresses metastases of melanomas and breast carcinomas without affecting tumorigenicity. The encoded protein may inhibit chemotaxis and invasion and thereby attenuate metastasis in malignant melanomas. Studies suggest a putative role in the regulation of events downstream of cell-matrix adhesion, perhaps involving cytoskeletal reorganization. A protein product of this gene, kisspeptin, stimulates gonadotropin-releasing hormone (GnRH)-induced gonadotropin secretion and regulates the pubertal activation of GnRH nuerons. A polymorphism in the terminal exon of this mRNA results in two protein isoforms. An adenosine present at the polymorphic site represents the third position in a stop codon. When the adenosine is absent, a downstream stop codon is utilized and the encoded protein extends for an additional seven amino acid residues. [provided by RefSeq, Mar 2012]","start":204190341,"end":204196486,"strand":-1,"description":"KiSS-1 metastasis-suppressor [Source:HGNC Symbol;Acc:HGNC:6341]"}, {"versioned_ensembl_gene_id":"ENSG00000166682.10","gene_symbol":"TMPRSS5","gene_name":"transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]","synonyms":"MGC148044,MGC141886","biotype":"protein_coding","ncbi_id":"80975","summary":"This gene encodes a protein that belongs to the serine protease family. Serine proteases are known to be involved in many physiological and pathological processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":113687550,"end":113706373,"strand":-1,"description":"transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]"}, {"versioned_ensembl_gene_id":"ENSG00000131495.8","gene_symbol":"NDUFA2","gene_name":"NADH:ubiquinone oxidoreductase subunit A2 [Source:HGNC Symbol;Acc:HGNC:7685]","synonyms":"B8","biotype":"protein_coding","ncbi_id":"4695","summary":"The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":140638740,"end":140647785,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A2 [Source:HGNC Symbol;Acc:HGNC:7685]"}, {"versioned_ensembl_gene_id":"ENSG00000214944.9","gene_symbol":"ARHGEF28","gene_name":"Rho guanine nucleotide exchange factor 28 [Source:HGNC Symbol;Acc:HGNC:30322]","synonyms":"RIP2,RGNEF,p190RhoGEF","biotype":"protein_coding","ncbi_id":"64283","summary":"This gene encodes a member of the Rho guanine nucleotide exchange factor family. The encoded protein interacts with low molecular weight neurofilament mRNA and may be involved in the formation of amyotrophic lateral sclerosis neurofilament aggregates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":73626158,"end":73941993,"strand":1,"description":"Rho guanine nucleotide exchange factor 28 [Source:HGNC Symbol;Acc:HGNC:30322]"}, {"versioned_ensembl_gene_id":"ENSG00000126461.14","gene_symbol":"SCAF1","gene_name":"SR-related CTD associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30403]","synonyms":"SR-A1,FLJ00034","biotype":"protein_coding","ncbi_id":"58506","summary":null,"start":49642125,"end":49658642,"strand":1,"description":"SR-related CTD associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30403]"}, {"versioned_ensembl_gene_id":"ENSG00000251365.1","gene_symbol":"AC122710.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6765891,"end":6771953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188032.9","gene_symbol":"C19orf67","gene_name":"chromosome 19 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:34354]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646457","summary":null,"start":14081619,"end":14085875,"strand":-1,"description":"chromosome 19 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:34354]"}, {"versioned_ensembl_gene_id":"ENSG00000243388.1","gene_symbol":"RPL3P3","gene_name":"ribosomal protein L3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23550]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645798","summary":null,"start":56978409,"end":56979621,"strand":1,"description":"ribosomal protein L3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23550]"}, {"versioned_ensembl_gene_id":"ENSG00000269846.1","gene_symbol":"AL136172.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37095785,"end":37097178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260912.1","gene_symbol":"AL158206.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":19453209,"end":19455173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188710.2","gene_symbol":"QRFP","gene_name":"pyroglutamylated RFamide peptide [Source:HGNC Symbol;Acc:HGNC:29982]","synonyms":"P518,26RFa","biotype":"protein_coding","ncbi_id":"347148","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. The encoded products are members of the RFamide family of neuropeptides, characterized by their common protein C-terminus consisting of an arginine (R) and an amidated phenylalanine (F). These products include the neuropeptides 26RFa and the N-terminally extended form, 43RFa. Both of these neuropeptides bind to the pyroglutamylated RFamide peptide receptor (QRFPR) and may regulate blood pressure, reproduction and food intake in rodents. [provided by RefSeq, Jul 2015]","start":130892702,"end":130896812,"strand":-1,"description":"pyroglutamylated RFamide peptide [Source:HGNC Symbol;Acc:HGNC:29982]"}, {"versioned_ensembl_gene_id":"ENSG00000234915.1","gene_symbol":"AL360091.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":212299495,"end":212331713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230063.1","gene_symbol":"AL360091.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":212297448,"end":212299579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126460.10","gene_symbol":"PRRG2","gene_name":"proline rich and Gla domain 2 [Source:HGNC Symbol;Acc:HGNC:9470]","synonyms":"PRGP2","biotype":"protein_coding","ncbi_id":"5639","summary":"The protein encoded by this gene is a single-pass transmembrane protein containing an N-terminal gamma-carboxyglutamic acid (Gla) domain and tandem Pro/Leu-Pro-Xaa-Tyr (PY) motifs at its C-terminal end. The Gla domain is exposed on the cell surface while the PY motifs are cytoplasmic. The PY motifs of the encoded protein have been shown to interact with YAP1, a WW domain-containing protein. Therefore, it is thought that the encoded protein may be part of a signal transduction pathway. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":49580646,"end":49591015,"strand":1,"description":"proline rich and Gla domain 2 [Source:HGNC Symbol;Acc:HGNC:9470]"}, {"versioned_ensembl_gene_id":"ENSG00000205476.8","gene_symbol":"CCDC85C","gene_name":"coiled-coil domain containing 85C [Source:HGNC Symbol;Acc:HGNC:35459]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317762","summary":null,"start":99500180,"end":99604026,"strand":-1,"description":"coiled-coil domain containing 85C [Source:HGNC Symbol;Acc:HGNC:35459]"}, {"versioned_ensembl_gene_id":"ENSG00000137496.17","gene_symbol":"IL18BP","gene_name":"interleukin 18 binding protein [Source:HGNC Symbol;Acc:HGNC:5987]","synonyms":"IL18BPa","biotype":"protein_coding","ncbi_id":"10068","summary":"The protein encoded by this gene functions as an inhibitor of the proinflammatory cytokine, IL18. It binds IL18, prevents the binding of IL18 to its receptor, and thus inhibits IL18-induced IFN-gamma production, resulting in reduced T-helper type 1 immune responses. This protein is constitutively expressed and secreted in mononuclear cells. Elevated level of this protein is detected in the intestinal tissues of patients with Crohn's disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":71998541,"end":72005715,"strand":1,"description":"interleukin 18 binding protein [Source:HGNC Symbol;Acc:HGNC:5987]"}, {"versioned_ensembl_gene_id":"ENSG00000108018.15","gene_symbol":"SORCS1","gene_name":"sortilin related VPS10 domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:16697]","synonyms":"sorCS1","biotype":"protein_coding","ncbi_id":"114815","summary":"This gene encodes one family member of vacuolar protein sorting 10 (VPS10) domain-containing receptor proteins. The VPS10 domain name comes from the yeast carboxypeptidase Y sorting receptor Vps10 protein. Members of this gene family are large with many exons but the CDS lengths are usually less than 3700 nt. Very large introns typically separate the exons encoding the VPS10 domain; the remaining exons are separated by much smaller-sized introns. These genes are strongly expressed in the central nervous system. Two of the five family members (sortilin and sortilin-related receptor) are synthesized as preproproteins; it is not yet known if this encoded protein is also a preproprotein. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":106573663,"end":107164534,"strand":-1,"description":"sortilin related VPS10 domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:16697]"}, {"versioned_ensembl_gene_id":"ENSG00000186765.11","gene_symbol":"FSCN2","gene_name":"fascin actin-bundling protein 2, retinal [Source:HGNC Symbol;Acc:HGNC:3960]","synonyms":"RP30,RFSN","biotype":"protein_coding","ncbi_id":"25794","summary":"This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":81528396,"end":81537130,"strand":1,"description":"fascin actin-bundling protein 2, retinal [Source:HGNC Symbol;Acc:HGNC:3960]"}, {"versioned_ensembl_gene_id":"ENSG00000247993.2","gene_symbol":"FOXD1-AS1","gene_name":"FOXD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50658]","synonyms":"TCONS_00009423","biotype":"lincRNA","ncbi_id":"106144539","summary":null,"start":73446357,"end":73446984,"strand":1,"description":"FOXD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50658]"}, {"versioned_ensembl_gene_id":"ENSG00000267394.1","gene_symbol":"AC004596.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44198882,"end":44216565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260793.2","gene_symbol":"AC003102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44221401,"end":44223710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267080.5","gene_symbol":"ASB16-AS1","gene_name":"ASB16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25442]","synonyms":"DKFZp762C2414,C17orf65","biotype":"antisense_RNA","ncbi_id":"339201","summary":null,"start":44175973,"end":44186717,"strand":-1,"description":"ASB16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25442]"}, {"versioned_ensembl_gene_id":"ENSG00000120306.9","gene_symbol":"CYSTM1","gene_name":"cysteine rich transmembrane module containing 1 [Source:HGNC Symbol;Acc:HGNC:30239]","synonyms":"ORF1-FL49,C5orf32","biotype":"protein_coding","ncbi_id":"84418","summary":null,"start":140174642,"end":140282052,"strand":1,"description":"cysteine rich transmembrane module containing 1 [Source:HGNC Symbol;Acc:HGNC:30239]"}, {"versioned_ensembl_gene_id":"ENSG00000137731.13","gene_symbol":"FXYD2","gene_name":"FXYD domain containing ion transport regulator 2 [Source:HGNC Symbol;Acc:HGNC:4026]","synonyms":"MGC12372,HOMG2,ATP1G1","biotype":"protein_coding","ncbi_id":"486","summary":"This gene encodes a member of the FXYD family of transmembrane proteins. This particular protein encodes the sodium/potassium-transporting ATPase subunit gamma. Mutations in this gene have been associated with Renal Hypomagnesemia-2. Alternatively spliced transcript variants have been described. Read-through transcripts have been observed between this locus and the upstream FXYD domain-containing ion transport regulator 6 (FXYD6, GeneID 53826) locus.[provided by RefSeq, Feb 2011]","start":117800844,"end":117828698,"strand":-1,"description":"FXYD domain containing ion transport regulator 2 [Source:HGNC Symbol;Acc:HGNC:4026]"}, {"versioned_ensembl_gene_id":"ENSG00000262833.1","gene_symbol":"AC016245.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80801640,"end":80805632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236733.1","gene_symbol":"AL354794.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68822403,"end":68843275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090554.12","gene_symbol":"FLT3LG","gene_name":"fms related tyrosine kinase 3 ligand [Source:HGNC Symbol;Acc:HGNC:3766]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2323","summary":"Dendritic cells (DCs) provide the key link between innate and adaptive immunity by recognizing pathogens and priming pathogen-specific immune responses. FLT3LG controls the development of DCs and is particularly important for plasmacytoid DCs and CD8 (see MIM 186910)-positive classical DCs and their CD103 (ITGAE; MIM 604682)-positive tissue counterparts (summary by Sathaliyawala et al., 2010 [PubMed 20933441]).[supplied by OMIM, Jan 2011]","start":49474207,"end":49486231,"strand":1,"description":"fms related tyrosine kinase 3 ligand [Source:HGNC Symbol;Acc:HGNC:3766]"}, {"versioned_ensembl_gene_id":"ENSG00000177103.13","gene_symbol":"DSCAML1","gene_name":"DS cell adhesion molecule like 1 [Source:HGNC Symbol;Acc:HGNC:14656]","synonyms":"KIAA1132","biotype":"protein_coding","ncbi_id":"57453","summary":"The protein encoded by this gene is a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016]","start":117427773,"end":117817525,"strand":-1,"description":"DS cell adhesion molecule like 1 [Source:HGNC Symbol;Acc:HGNC:14656]"}, {"versioned_ensembl_gene_id":"ENSG00000165914.14","gene_symbol":"TTC7B","gene_name":"tetratricopeptide repeat domain 7B [Source:HGNC Symbol;Acc:HGNC:19858]","synonyms":"TTC7L1","biotype":"protein_coding","ncbi_id":"145567","summary":null,"start":90524564,"end":90816479,"strand":-1,"description":"tetratricopeptide repeat domain 7B [Source:HGNC Symbol;Acc:HGNC:19858]"}, {"versioned_ensembl_gene_id":"ENSG00000141564.13","gene_symbol":"RPTOR","gene_name":"regulatory associated protein of MTOR complex 1 [Source:HGNC Symbol;Acc:HGNC:30287]","synonyms":"KIAA1303,raptor,Mip1,KOG1","biotype":"protein_coding","ncbi_id":"57521","summary":"This gene encodes a component of a signaling pathway that regulates cell growth in response to nutrient and insulin levels. The encoded protein forms a stoichiometric complex with the mTOR kinase, and also associates with eukaryotic initiation factor 4E-binding protein-1 and ribosomal protein S6 kinase. The protein positively regulates the downstream effector ribosomal protein S6 kinase, and negatively regulates the mTOR kinase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":80544819,"end":80966371,"strand":1,"description":"regulatory associated protein of MTOR complex 1 [Source:HGNC Symbol;Acc:HGNC:30287]"}, {"versioned_ensembl_gene_id":"ENSG00000266925.1","gene_symbol":"AC015818.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20507413,"end":20508931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279588.2","gene_symbol":"AC087762.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":100782417,"end":100786189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198040.10","gene_symbol":"ZNF84","gene_name":"zinc finger protein 84 [Source:HGNC Symbol;Acc:HGNC:13159]","synonyms":"HPF2","biotype":"protein_coding","ncbi_id":"7637","summary":null,"start":133037292,"end":133063304,"strand":1,"description":"zinc finger protein 84 [Source:HGNC Symbol;Acc:HGNC:13159]"}, {"versioned_ensembl_gene_id":"ENSG00000242837.1","gene_symbol":"RPL21P13","gene_name":"ribosomal protein L21 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:19812]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319144","summary":null,"start":103241492,"end":103241972,"strand":1,"description":"ribosomal protein L21 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:19812]"}, {"versioned_ensembl_gene_id":"ENSG00000187742.14","gene_symbol":"SECISBP2","gene_name":"SECIS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30972]","synonyms":"SBP2","biotype":"protein_coding","ncbi_id":"79048","summary":"The protein encoded by this gene is one of the essential components of the machinery involved in co-translational insertion of selenocysteine (Sec) into selenoproteins. Sec is encoded by the UGA codon, which normally signals translation termination. The recoding of UGA as Sec codon requires a Sec insertion sequence (SECIS) element; present in the 3' untranslated regions of eukaryotic selenoprotein mRNAs. This protein specifically binds to the SECIS element, which is stimulated by a Sec-specific translation elongation factor. Mutations in this gene have been associated with reduction in enzymatic activity of type II iodothyronine deiodinase (a selenoprotein) and abnormal thyroid hormone metabolism. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]","start":89318506,"end":89359662,"strand":1,"description":"SECIS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30972]"}, {"versioned_ensembl_gene_id":"ENSG00000146242.8","gene_symbol":"TPBG","gene_name":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]","synonyms":"5T4-AG,5T4","biotype":"protein_coding","ncbi_id":"7162","summary":"This gene encodes a leucine-rich transmembrane glycoprotein that may be involved in cell adhesion. The encoded protein is an oncofetal antigen that is specific to trophoblast cells. In adults this protein is highly expressed in many tumor cells and is associated with poor clinical outcome in numerous cancers. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]","start":82363206,"end":82370828,"strand":1,"description":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]"}, {"versioned_ensembl_gene_id":"ENSG00000250490.1","gene_symbol":"LINC02145","gene_name":"long intergenic non-protein coding RNA 2145 [Source:HGNC Symbol;Acc:HGNC:53005]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401172","summary":null,"start":6310441,"end":6339884,"strand":-1,"description":"long intergenic non-protein coding RNA 2145 [Source:HGNC Symbol;Acc:HGNC:53005]"}, {"versioned_ensembl_gene_id":"ENSG00000101336.13","gene_symbol":"HCK","gene_name":"HCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4840]","synonyms":"JTK9","biotype":"protein_coding","ncbi_id":"3055","summary":"The protein encoded by this gene is a member of the Src family of tyrosine kinases. This protein is primarily hemopoietic, particularly in cells of the myeloid and B-lymphoid lineages. It may help couple the Fc receptor to the activation of the respiratory burst. In addition, it may play a role in neutrophil migration and in the degranulation of neutrophils. Multiple isoforms with different subcellular distributions are produced due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) codon. [provided by RefSeq, Feb 2010]","start":32052188,"end":32101856,"strand":1,"description":"HCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4840]"}, {"versioned_ensembl_gene_id":"ENSG00000271904.1","gene_symbol":"AC091826.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88433892,"end":88498697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248172.1","gene_symbol":"AC009720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49996889,"end":50016844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143476.17","gene_symbol":"DTL","gene_name":"denticleless E3 ubiquitin protein ligase homolog [Source:HGNC Symbol;Acc:HGNC:30288]","synonyms":"RAMP,L2DTL,DCAF2,CDT2","biotype":"protein_coding","ncbi_id":"51514","summary":null,"start":212035553,"end":212107400,"strand":1,"description":"denticleless E3 ubiquitin protein ligase homolog [Source:HGNC Symbol;Acc:HGNC:30288]"}, {"versioned_ensembl_gene_id":"ENSG00000148344.10","gene_symbol":"PTGES","gene_name":"prostaglandin E synthase [Source:HGNC Symbol;Acc:HGNC:9599]","synonyms":"MGST1L1,MGST1-L1,MGST-IV,TP53I12,PIG12","biotype":"protein_coding","ncbi_id":"9536","summary":"The protein encoded by this gene is a glutathione-dependent prostaglandin E synthase. The expression of this gene has been shown to be induced by proinflammatory cytokine interleukin 1 beta (IL1B). Its expression can also be induced by tumor suppressor protein TP53, and may be involved in TP53 induced apoptosis. Knockout studies in mice suggest that this gene may contribute to the pathogenesis of collagen-induced arthritis and mediate acute pain during inflammatory responses. [provided by RefSeq, Jul 2008]","start":129738331,"end":129753047,"strand":-1,"description":"prostaglandin E synthase [Source:HGNC Symbol;Acc:HGNC:9599]"}, {"versioned_ensembl_gene_id":"ENSG00000260220.6","gene_symbol":"CCDC187","gene_name":"coiled-coil domain containing 187 [Source:HGNC Symbol;Acc:HGNC:30942]","synonyms":"MGC50722","biotype":"protein_coding","ncbi_id":"399693","summary":null,"start":136249971,"end":136306901,"strand":-1,"description":"coiled-coil domain containing 187 [Source:HGNC Symbol;Acc:HGNC:30942]"}, {"versioned_ensembl_gene_id":"ENSG00000279813.1","gene_symbol":"CR392000.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":136249978,"end":136251205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254593.1","gene_symbol":"OR7E126P","gene_name":"olfactory receptor family 7 subfamily E member 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:15304]","synonyms":"OR11-1,hg500","biotype":"unprocessed_pseudogene","ncbi_id":"81176","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71903194,"end":71904081,"strand":1,"description":"olfactory receptor family 7 subfamily E member 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:15304]"}, {"versioned_ensembl_gene_id":"ENSG00000167157.10","gene_symbol":"PRRX2","gene_name":"paired related homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21338]","synonyms":"PRX2,PMX2","biotype":"protein_coding","ncbi_id":"51450","summary":"The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins. Expression is localized to proliferating fetal fibroblasts and the developing dermal layer, with downregulated expression in adult skin. Increases in expression of this gene during fetal but not adult wound healing suggest a possible role in mechanisms that control mammalian dermal regeneration and prevent formation of scar response to wounding. The expression patterns provide evidence consistent with a role in fetal skin development and a possible role in cellular proliferation. [provided by RefSeq, Jul 2008]","start":129665641,"end":129722674,"strand":1,"description":"paired related homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21338]"}, {"versioned_ensembl_gene_id":"ENSG00000213315.5","gene_symbol":"AL122020.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90766531,"end":90766989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227987.1","gene_symbol":"AC092675.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":98346995,"end":98351140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251066.1","gene_symbol":"AC026700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85549409,"end":85549952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272696.1","gene_symbol":"AL359091.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128316337,"end":128316909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153832.11","gene_symbol":"FBXO36","gene_name":"F-box protein 36 [Source:HGNC Symbol;Acc:HGNC:27020]","synonyms":"FLJ37592,Fbx36","biotype":"protein_coding","ncbi_id":"130888","summary":"Members of the F-box protein family, such as FBXO36, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":229922302,"end":230013109,"strand":1,"description":"F-box protein 36 [Source:HGNC Symbol;Acc:HGNC:27020]"}, {"versioned_ensembl_gene_id":"ENSG00000236024.1","gene_symbol":"PRRX2-AS1","gene_name":"PRRX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50684]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929437","summary":null,"start":129712896,"end":129718635,"strand":-1,"description":"PRRX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50684]"}, {"versioned_ensembl_gene_id":"ENSG00000165661.16","gene_symbol":"QSOX2","gene_name":"quiescin sulfhydryl oxidase 2 [Source:HGNC Symbol;Acc:HGNC:30249]","synonyms":"SOXN,QSCN6L1,DKFZp762A2013","biotype":"protein_coding","ncbi_id":"169714","summary":"QSOX2 is a member of the sulfhydryl oxidase/quiescin-6 (Q6) family (QSOX1; MIM 603120) that regulates the sensitization of neuroblastoma cells for IFN-gamma (IFNG; MIM 147570)-induced cell death (Wittke et al., 2003 [PubMed 14633699]).[supplied by OMIM, Jun 2009]","start":136206333,"end":136245841,"strand":-1,"description":"quiescin sulfhydryl oxidase 2 [Source:HGNC Symbol;Acc:HGNC:30249]"}, {"versioned_ensembl_gene_id":"ENSG00000107187.15","gene_symbol":"LHX3","gene_name":"LIM homeobox 3 [Source:HGNC Symbol;Acc:HGNC:6595]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8022","summary":"This gene encodes a member of a large family of proteins which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene cause combined pituitary hormone deficiency 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":136196250,"end":136205109,"strand":-1,"description":"LIM homeobox 3 [Source:HGNC Symbol;Acc:HGNC:6595]"}, {"versioned_ensembl_gene_id":"ENSG00000249689.1","gene_symbol":"AC138517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139492538,"end":139493105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232347.1","gene_symbol":"AL390728.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":247210691,"end":247241823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233901.5","gene_symbol":"LINC01503","gene_name":"long intergenic non-protein coding RNA 1503 [Source:HGNC Symbol;Acc:HGNC:51184]","synonyms":"lnc-PPP2R4-5","biotype":"lincRNA","ncbi_id":"100506119","summary":null,"start":129332300,"end":129359538,"strand":1,"description":"long intergenic non-protein coding RNA 1503 [Source:HGNC Symbol;Acc:HGNC:51184]"}, {"versioned_ensembl_gene_id":"ENSG00000241084.1","gene_symbol":"AL161785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129259062,"end":129261581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235007.2","gene_symbol":"AL161785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129258354,"end":129259846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263873.1","gene_symbol":"AP003396.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":119417951,"end":119419114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244062.1","gene_symbol":"AC080128.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133760300,"end":133762363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130348.11","gene_symbol":"QRSL1","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 [Source:HGNC Symbol;Acc:HGNC:21020]","synonyms":"GatA,FLJ13447,FLJ12189,FLJ10989,DKFZP564C1278","biotype":"protein_coding","ncbi_id":"55278","summary":null,"start":106629578,"end":106668417,"strand":1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 [Source:HGNC Symbol;Acc:HGNC:21020]"}, {"versioned_ensembl_gene_id":"ENSG00000181619.11","gene_symbol":"GPR135","gene_name":"G protein-coupled receptor 135 [Source:HGNC Symbol;Acc:HGNC:19991]","synonyms":"PAFR,HUMNPIIY20","biotype":"protein_coding","ncbi_id":"64582","summary":null,"start":59429022,"end":59465342,"strand":-1,"description":"G protein-coupled receptor 135 [Source:HGNC Symbol;Acc:HGNC:19991]"}, {"versioned_ensembl_gene_id":"ENSG00000258782.3","gene_symbol":"AL121694.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":59479274,"end":59525437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151838.11","gene_symbol":"CCDC175","gene_name":"coiled-coil domain containing 175 [Source:HGNC Symbol;Acc:HGNC:19847]","synonyms":"C14orf38","biotype":"protein_coding","ncbi_id":"729665","summary":null,"start":59504539,"end":59576831,"strand":-1,"description":"coiled-coil domain containing 175 [Source:HGNC Symbol;Acc:HGNC:19847]"}, {"versioned_ensembl_gene_id":"ENSG00000273891.1","gene_symbol":"AL731566.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121965764,"end":121967700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204571.6","gene_symbol":"KRTAP5-11","gene_name":"keratin associated protein 5-11 [Source:HGNC Symbol;Acc:HGNC:23606]","synonyms":"KRTAP5.11,KRTAP5-6","biotype":"protein_coding","ncbi_id":"440051","summary":null,"start":71579714,"end":71603353,"strand":-1,"description":"keratin associated protein 5-11 [Source:HGNC Symbol;Acc:HGNC:23606]"}, {"versioned_ensembl_gene_id":"ENSG00000073008.14","gene_symbol":"PVR","gene_name":"poliovirus receptor [Source:HGNC Symbol;Acc:HGNC:9705]","synonyms":"Tage4,PVS,NECL5,Necl-5,HVED,CD155","biotype":"protein_coding","ncbi_id":"5817","summary":"The protein encoded by this gene is a transmembrane glycoprotein belonging to the immunoglobulin superfamily. The external domain mediates cell attachment to the extracellular matrix molecule vitronectin, while its intracellular domain interacts with the dynein light chain Tctex-1/DYNLT1. The gene is specific to the primate lineage, and serves as a cellular receptor for poliovirus in the first step of poliovirus replication. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":44643798,"end":44663583,"strand":1,"description":"poliovirus receptor [Source:HGNC Symbol;Acc:HGNC:9705]"}, {"versioned_ensembl_gene_id":"ENSG00000276206.1","gene_symbol":"AC012314.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54031412,"end":54031504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163781.12","gene_symbol":"TOPBP1","gene_name":"topoisomerase (DNA) II binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17008]","synonyms":"TOP2BP1,KIAA0259","biotype":"protein_coding","ncbi_id":"11073","summary":"This gene encodes a binding protein which interacts with the C-terminal region of topoisomerase II beta. This interaction suggests a supportive role for this protein in the catalytic reactions of topoisomerase II beta through transient breakages of DNA strands. [provided by RefSeq, Jul 2008]","start":133598175,"end":133661893,"strand":-1,"description":"topoisomerase (DNA) II binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17008]"}, {"versioned_ensembl_gene_id":"ENSG00000249994.1","gene_symbol":"AC025187.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4033713,"end":4041764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255191.1","gene_symbol":"AP003555.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69985876,"end":70015815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186895.2","gene_symbol":"FGF3","gene_name":"fibroblast growth factor 3 [Source:HGNC Symbol;Acc:HGNC:3681]","synonyms":"INT2,HBGF-3","biotype":"protein_coding","ncbi_id":"2248","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its similarity with mouse fgf3/int-2, a proto-oncogene activated in virally induced mammary tumors in the mouse. Frequent amplification of this gene has been found in human tumors, which may be important for neoplastic transformation and tumor progression. Studies of the similar genes in mouse and chicken suggested the role in inner ear formation. [provided by RefSeq, Jul 2008]","start":69810224,"end":69819024,"strand":-1,"description":"fibroblast growth factor 3 [Source:HGNC Symbol;Acc:HGNC:3681]"}, {"versioned_ensembl_gene_id":"ENSG00000260348.1","gene_symbol":"AP007216.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69909184,"end":69910994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245552.6","gene_symbol":"AP000787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95150539,"end":95234104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186451.1","gene_symbol":"SPATA12","gene_name":"spermatogenesis associated 12 [Source:HGNC Symbol;Acc:HGNC:23221]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353324","summary":"This gene is expressed primarily in testis and may play a role in testicular development and spermatogenesis. The encoded protein may be upregulated in response to ultraviolet-C radiation. [provided by RefSeq, Dec 2015]","start":57060441,"end":57075432,"strand":1,"description":"spermatogenesis associated 12 [Source:HGNC Symbol;Acc:HGNC:23221]"}, {"versioned_ensembl_gene_id":"ENSG00000248477.6","gene_symbol":"AC139495.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69607099,"end":69624049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111962.7","gene_symbol":"UST","gene_name":"uronyl 2-sulfotransferase [Source:HGNC Symbol;Acc:HGNC:17223]","synonyms":"2OST","biotype":"protein_coding","ncbi_id":"10090","summary":"Uronyl 2-sulfotransferase transfers sulfate to the 2-position of uronyl residues, such as iduronyl residues in dermatan sulfate and glucuronyl residues in chondroitin sulfate (Kobayashi et al., 1999 [PubMed 10187838]).[supplied by OMIM, Mar 2008]","start":148747328,"end":149076990,"strand":1,"description":"uronyl 2-sulfotransferase [Source:HGNC Symbol;Acc:HGNC:17223]"}, {"versioned_ensembl_gene_id":"ENSG00000259136.1","gene_symbol":"AL137100.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57044646,"end":57044960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182544.8","gene_symbol":"MFSD5","gene_name":"major facilitator superfamily domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28156]","synonyms":"MGC11308","biotype":"protein_coding","ncbi_id":"84975","summary":null,"start":53251251,"end":53254405,"strand":1,"description":"major facilitator superfamily domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28156]"}, {"versioned_ensembl_gene_id":"ENSG00000248107.1","gene_symbol":"LINC02039","gene_name":"long intergenic non-protein coding RNA 2039 [Source:HGNC Symbol;Acc:HGNC:52879]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546228","summary":null,"start":126179577,"end":126193850,"strand":1,"description":"long intergenic non-protein coding RNA 2039 [Source:HGNC Symbol;Acc:HGNC:52879]"}, {"versioned_ensembl_gene_id":"ENSG00000269037.1","gene_symbol":"LINC01838","gene_name":"long intergenic non-protein coding RNA 1838 [Source:HGNC Symbol;Acc:HGNC:52654]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652911","summary":null,"start":34905315,"end":34908188,"strand":1,"description":"long intergenic non-protein coding RNA 1838 [Source:HGNC Symbol;Acc:HGNC:52654]"}, {"versioned_ensembl_gene_id":"ENSG00000262495.1","gene_symbol":"AC012146.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5060356,"end":5062123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152315.4","gene_symbol":"KCNK13","gene_name":"potassium two pore domain channel subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:6275]","synonyms":"K2p13.1,THIK1,THIK-1","biotype":"protein_coding","ncbi_id":"56659","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a potassium channel containing two pore-forming domains. This protein is an open channel that can be stimulated by arachidonic acid and inhibited by the anesthetic halothane. [provided by RefSeq, Jul 2013]","start":90061765,"end":90185857,"strand":1,"description":"potassium two pore domain channel subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:6275]"}, {"versioned_ensembl_gene_id":"ENSG00000197822.10","gene_symbol":"OCLN","gene_name":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]","synonyms":"PPP1R115","biotype":"protein_coding","ncbi_id":"100506658","summary":"This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]","start":69492292,"end":69558104,"strand":1,"description":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]"}, {"versioned_ensembl_gene_id":"ENSG00000255947.1","gene_symbol":"AP002754.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61654665,"end":61655702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197380.10","gene_symbol":"DACT3","gene_name":"dishevelled binding antagonist of beta catenin 3 [Source:HGNC Symbol;Acc:HGNC:30745]","synonyms":"RRR1,MGC15476,DAPPER3","biotype":"protein_coding","ncbi_id":"147906","summary":null,"start":46647612,"end":46661138,"strand":-1,"description":"dishevelled binding antagonist of beta catenin 3 [Source:HGNC Symbol;Acc:HGNC:30745]"}, {"versioned_ensembl_gene_id":"ENSG00000122378.13","gene_symbol":"FAM213A","gene_name":"family with sequence similarity 213 member A [Source:HGNC Symbol;Acc:HGNC:28651]","synonyms":"PAMM,MGC4248,C10orf58,Adrx","biotype":"protein_coding","ncbi_id":"84293","summary":null,"start":80407829,"end":80437115,"strand":1,"description":"family with sequence similarity 213 member A [Source:HGNC Symbol;Acc:HGNC:28651]"}, {"versioned_ensembl_gene_id":"ENSG00000277382.1","gene_symbol":"AC005837.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76709760,"end":76710045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095203.14","gene_symbol":"EPB41L4B","gene_name":"erythrocyte membrane protein band 4.1 like 4B [Source:HGNC Symbol;Acc:HGNC:19818]","synonyms":"EHM2","biotype":"protein_coding","ncbi_id":"54566","summary":null,"start":109171975,"end":109320964,"strand":-1,"description":"erythrocyte membrane protein band 4.1 like 4B [Source:HGNC Symbol;Acc:HGNC:19818]"}, {"versioned_ensembl_gene_id":"ENSG00000277176.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54831023,"end":54842954,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000213954.3","gene_symbol":"ATP5HP3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"138864","summary":null,"start":14068932,"end":14069417,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49625]"}, {"versioned_ensembl_gene_id":"ENSG00000270175.1","gene_symbol":"AC023509.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53500162,"end":53500936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284725.1","gene_symbol":"AC093762.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227724440,"end":227724757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163092.19","gene_symbol":"XIRP2","gene_name":"xin actin binding repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14303]","synonyms":"CMYA3","biotype":"protein_coding","ncbi_id":"129446","summary":null,"start":166888487,"end":167259753,"strand":1,"description":"xin actin binding repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14303]"}, {"versioned_ensembl_gene_id":"ENSG00000269119.1","gene_symbol":"HNRNPA1P52","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:48782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645001","summary":null,"start":41829692,"end":41830938,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:48782]"}, {"versioned_ensembl_gene_id":"ENSG00000267173.1","gene_symbol":"AC245748.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":44329695,"end":44401608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254933.1","gene_symbol":"AP000785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76190725,"end":76195071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057657.15","gene_symbol":"PRDM1","gene_name":"PR/SET domain 1 [Source:HGNC Symbol;Acc:HGNC:9346]","synonyms":"PRDI-BF1,BLIMP1","biotype":"protein_coding","ncbi_id":"639","summary":"This gene encodes a protein that acts as a repressor of beta-interferon gene expression. The protein binds specifically to the PRDI (positive regulatory domain I element) of the beta-IFN gene promoter. Transcription of this gene increases upon virus induction. Two alternatively spliced transcript variants that encode different isoforms have been reported. [provided by RefSeq, Jul 2008]","start":106086320,"end":106109939,"strand":1,"description":"PR/SET domain 1 [Source:HGNC Symbol;Acc:HGNC:9346]"}, {"versioned_ensembl_gene_id":"ENSG00000248600.1","gene_symbol":"AC025465.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124455373,"end":124460098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198342.9","gene_symbol":"ZNF442","gene_name":"zinc finger protein 442 [Source:HGNC Symbol;Acc:HGNC:20877]","synonyms":"FLJ14356","biotype":"protein_coding","ncbi_id":"79973","summary":null,"start":12345949,"end":12365905,"strand":-1,"description":"zinc finger protein 442 [Source:HGNC Symbol;Acc:HGNC:20877]"}, {"versioned_ensembl_gene_id":"ENSG00000267518.1","gene_symbol":"AC090699.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76345761,"end":76346081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228157.4","gene_symbol":"AC007952.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19092974,"end":19096837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237523.1","gene_symbol":"LINC00857","gene_name":"long intergenic non-protein coding RNA 857 [Source:HGNC Symbol;Acc:HGNC:45114]","synonyms":null,"biotype":"lincRNA","ncbi_id":"439990","summary":null,"start":80207710,"end":80219657,"strand":1,"description":"long intergenic non-protein coding RNA 857 [Source:HGNC Symbol;Acc:HGNC:45114]"}, {"versioned_ensembl_gene_id":"ENSG00000161594.6","gene_symbol":"KLHL10","gene_name":"kelch like family member 10 [Source:HGNC Symbol;Acc:HGNC:18829]","synonyms":"FLJ32662","biotype":"protein_coding","ncbi_id":"317719","summary":"The protein encoded by this gene belongs to the kelch repeat-containing family, and contains an N-terminal BTB/POZ domain a BACK domain and six C-terminal kelch repeats. Kelch domains are thought to form a four stranded beta-sheet blade structure that can fold into a beta-propeller domain when multiple kelch repeats are found together. Mutations in this gene have been associated with oligozoospermia in some infertile males. [provided by RefSeq, Jul 2016]","start":41835685,"end":41848384,"strand":1,"description":"kelch like family member 10 [Source:HGNC Symbol;Acc:HGNC:18829]"}, {"versioned_ensembl_gene_id":"ENSG00000250862.1","gene_symbol":"HMGB1P29","gene_name":"high mobility group box 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39120]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873892","summary":null,"start":124220579,"end":124221077,"strand":-1,"description":"high mobility group box 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39120]"}, {"versioned_ensembl_gene_id":"ENSG00000251421.2","gene_symbol":"AC016556.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124395603,"end":124400655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175093.4","gene_symbol":"SPSB4","gene_name":"splA/ryanodine receptor domain and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:30630]","synonyms":"SSB-4","biotype":"protein_coding","ncbi_id":"92369","summary":null,"start":141051402,"end":141148611,"strand":1,"description":"splA/ryanodine receptor domain and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:30630]"}, {"versioned_ensembl_gene_id":"ENSG00000266258.1","gene_symbol":"LINC01909","gene_name":"long intergenic non-protein coding RNA 1909 [Source:HGNC Symbol;Acc:HGNC:52728]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927481","summary":null,"start":70335439,"end":70352459,"strand":1,"description":"long intergenic non-protein coding RNA 1909 [Source:HGNC Symbol;Acc:HGNC:52728]"}, {"versioned_ensembl_gene_id":"ENSG00000231944.1","gene_symbol":"PHKA1-AS1","gene_name":"PHKA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40446]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928259","summary":null,"start":72688950,"end":72712348,"strand":1,"description":"PHKA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40446]"}, {"versioned_ensembl_gene_id":"ENSG00000268683.1","gene_symbol":"AC020910.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34638122,"end":34640689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152749.7","gene_symbol":"GPR180","gene_name":"G protein-coupled receptor 180 [Source:HGNC Symbol;Acc:HGNC:28899]","synonyms":"ITR","biotype":"protein_coding","ncbi_id":"160897","summary":"This gene encodes a protein that is a member of the G protein-coupled receptor superfamily. This protein is produced predominantly in vascular smooth muscle cells and may play an important role in the regulation of vascular remodeling. [provided by RefSeq, Jul 2008]","start":94601903,"end":94634645,"strand":1,"description":"G protein-coupled receptor 180 [Source:HGNC Symbol;Acc:HGNC:28899]"}, {"versioned_ensembl_gene_id":"ENSG00000241356.1","gene_symbol":"OR5G3","gene_name":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]","synonyms":"OR5G6P,OR5G3P","biotype":"polymorphic_pseudogene","ncbi_id":"81193","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56819576,"end":56820504,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]"}, {"versioned_ensembl_gene_id":"ENSG00000253149.3","gene_symbol":"AC245166.1","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106329432,"end":106329684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147654.14","gene_symbol":"EBAG9","gene_name":"estrogen receptor binding site associated, antigen, 9 [Source:HGNC Symbol;Acc:HGNC:3123]","synonyms":"RCAS1,EB9","biotype":"protein_coding","ncbi_id":"9166","summary":"This gene was identified as an estrogen-responsive gene. Regulation of transcription by estrogen is mediated by estrogen receptor, which binds to the estrogen-responsive element found in the 5'-flanking region of this gene. The encoded protein is a tumor-associated antigen that is expressed at high frequency in a variety of cancers. Alternate splicing results in multiple transcript variants. A pseudogene of this gene has been defined on chromosome 10. [provided by RefSeq, Jul 2013]","start":109539711,"end":109565996,"strand":1,"description":"estrogen receptor binding site associated, antigen, 9 [Source:HGNC Symbol;Acc:HGNC:3123]"}, {"versioned_ensembl_gene_id":"ENSG00000233707.3","gene_symbol":"RPL22P11","gene_name":"ribosomal protein L22 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35603]","synonyms":"RPL22P15","biotype":"processed_pseudogene","ncbi_id":"402100","summary":null,"start":109737139,"end":109737523,"strand":-1,"description":"ribosomal protein L22 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35603]"}, {"versioned_ensembl_gene_id":"ENSG00000250539.1","gene_symbol":"KRT8P33","gene_name":"keratin 8 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418737","summary":null,"start":123400922,"end":123402344,"strand":-1,"description":"keratin 8 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39867]"}, {"versioned_ensembl_gene_id":"ENSG00000151224.12","gene_symbol":"MAT1A","gene_name":"methionine adenosyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:6903]","synonyms":"SAMS1,SAMS,MATA1,MAT","biotype":"protein_coding","ncbi_id":"4143","summary":"This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency. [provided by RefSeq, Jul 2008]","start":80271820,"end":80289684,"strand":-1,"description":"methionine adenosyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:6903]"}, {"versioned_ensembl_gene_id":"ENSG00000255255.1","gene_symbol":"PPP1R1AP1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16316]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"94304","summary":null,"start":75911204,"end":75911628,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16316]"}, {"versioned_ensembl_gene_id":"ENSG00000255081.1","gene_symbol":"AP003168.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75914201,"end":75915213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235096.2","gene_symbol":"AC118555.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":246025897,"end":246035603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225222.2","gene_symbol":"CHCHD4P5","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479039","summary":null,"start":246178778,"end":246179204,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44493]"}, {"versioned_ensembl_gene_id":"ENSG00000284631.1","gene_symbol":"AC064853.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227616998,"end":227618655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175906.4","gene_symbol":"ARL4D","gene_name":"ADP ribosylation factor like GTPase 4D [Source:HGNC Symbol;Acc:HGNC:656]","synonyms":"ARF4L","biotype":"protein_coding","ncbi_id":"379","summary":"ADP-ribosylation factor 4D is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4D is closely similar to ARL4A and ARL4C and each has a nuclear localization signal and an unusually high guanine nucleotide exchange rate. This protein may play a role in membrane-associated intracellular trafficking. [provided by RefSeq, Jul 2021]","start":43398959,"end":43401137,"strand":1,"description":"ADP ribosylation factor like GTPase 4D [Source:HGNC Symbol;Acc:HGNC:656]"}, {"versioned_ensembl_gene_id":"ENSG00000244630.2","gene_symbol":"AC022493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80855507,"end":80855843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240973.1","gene_symbol":"AC093714.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115679345,"end":115682618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188825.13","gene_symbol":"LINC00910","gene_name":"long intergenic non-protein coding RNA 910 [Source:HGNC Symbol;Acc:HGNC:44361]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100130581","summary":null,"start":43369845,"end":43389199,"strand":-1,"description":"long intergenic non-protein coding RNA 910 [Source:HGNC Symbol;Acc:HGNC:44361]"}, {"versioned_ensembl_gene_id":"ENSG00000188878.19","gene_symbol":"FBF1","gene_name":"Fas binding factor 1 [Source:HGNC Symbol;Acc:HGNC:24674]","synonyms":"KIAA1863,FLJ00103,FBF-1,ALB","biotype":"protein_coding","ncbi_id":"85302","summary":null,"start":75909574,"end":75941140,"strand":-1,"description":"Fas binding factor 1 [Source:HGNC Symbol;Acc:HGNC:24674]"}, {"versioned_ensembl_gene_id":"ENSG00000242072.1","gene_symbol":"AC092590.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115647461,"end":115676329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132481.6","gene_symbol":"TRIM47","gene_name":"tripartite motif containing 47 [Source:HGNC Symbol;Acc:HGNC:19020]","synonyms":"RNF100,GOA","biotype":"protein_coding","ncbi_id":"91107","summary":null,"start":75874161,"end":75878575,"strand":-1,"description":"tripartite motif containing 47 [Source:HGNC Symbol;Acc:HGNC:19020]"}, {"versioned_ensembl_gene_id":"ENSG00000248969.1","gene_symbol":"AC137810.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35678484,"end":35827018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138376.10","gene_symbol":"BARD1","gene_name":"BRCA1 associated RING domain 1 [Source:HGNC Symbol;Acc:HGNC:952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"580","summary":"This gene encodes a protein which interacts with the N-terminal region of BRCA1. In addition to its ability to bind BRCA1 in vivo and in vitro, it shares homology with the 2 most conserved regions of BRCA1: the N-terminal RING motif and the C-terminal BRCT domain. The RING motif is a cysteine-rich sequence found in a variety of proteins that regulate cell growth, including the products of tumor suppressor genes and dominant protooncogenes. This protein also contains 3 tandem ankyrin repeats. The BARD1/BRCA1 interaction is disrupted by tumorigenic amino acid substitutions in BRCA1, implying that the formation of a stable complex between these proteins may be an essential aspect of BRCA1 tumor suppression. This protein may be the target of oncogenic mutations in breast or ovarian cancer. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":214725646,"end":214809711,"strand":-1,"description":"BRCA1 associated RING domain 1 [Source:HGNC Symbol;Acc:HGNC:952]"}, {"versioned_ensembl_gene_id":"ENSG00000080166.15","gene_symbol":"DCT","gene_name":"dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2709]","synonyms":"TYRP2","biotype":"protein_coding","ncbi_id":"1638","summary":null,"start":94436808,"end":94479682,"strand":-1,"description":"dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2709]"}, {"versioned_ensembl_gene_id":"ENSG00000143669.13","gene_symbol":"LYST","gene_name":"lysosomal trafficking regulator [Source:HGNC Symbol;Acc:HGNC:1968]","synonyms":"CHS,CHS1","biotype":"protein_coding","ncbi_id":"1130","summary":"This gene encodes a protein that regulates intracellular protein trafficking in endosomes, and may be involved in pigmentation. Mutations in this gene are associated with Chediak-Higashi syndrome, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants, though the full-length nature of some of these variants has not been determined. [provided by RefSeq, Apr 2013]","start":235661041,"end":235883640,"strand":-1,"description":"lysosomal trafficking regulator [Source:HGNC Symbol;Acc:HGNC:1968]"}, {"versioned_ensembl_gene_id":"ENSG00000268810.1","gene_symbol":"AC007193.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46382492,"end":46383169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235674.2","gene_symbol":"LDHAP2","gene_name":"lactate dehydrogenase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6537]","synonyms":"LDHAL2","biotype":"processed_pseudogene","ncbi_id":"100190799","summary":null,"start":235738005,"end":235738989,"strand":1,"description":"lactate dehydrogenase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6537]"}, {"versioned_ensembl_gene_id":"ENSG00000277596.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54727609,"end":54736462,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000238194.1","gene_symbol":"AL121908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59626464,"end":59628289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245954.6","gene_symbol":"LINC02273","gene_name":"long intergenic non-protein coding RNA 2273 [Source:HGNC Symbol;Acc:HGNC:53188]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996286","summary":null,"start":152100754,"end":152104720,"strand":1,"description":"long intergenic non-protein coding RNA 2273 [Source:HGNC Symbol;Acc:HGNC:53188]"}, {"versioned_ensembl_gene_id":"ENSG00000254101.5","gene_symbol":"LINC02055","gene_name":"long intergenic non-protein coding RNA 2055 [Source:HGNC Symbol;Acc:HGNC:52895]","synonyms":"RP1130-1","biotype":"lincRNA","ncbi_id":"107986980","summary":null,"start":136530798,"end":136984935,"strand":1,"description":"long intergenic non-protein coding RNA 2055 [Source:HGNC Symbol;Acc:HGNC:52895]"}, {"versioned_ensembl_gene_id":"ENSG00000230166.1","gene_symbol":"RPL35AP24","gene_name":"ribosomal protein L35a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271631","summary":null,"start":49909613,"end":49909942,"strand":1,"description":"ribosomal protein L35a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35544]"}, {"versioned_ensembl_gene_id":"ENSG00000144583.4","gene_symbol":"MARCH4","gene_name":"membrane associated ring-CH-type finger 4 [Source:HGNC Symbol;Acc:HGNC:29269]","synonyms":"RNF174,MARCH-IV,KIAA1399","biotype":"protein_coding","ncbi_id":"57574","summary":"MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010]","start":216257865,"end":216372027,"strand":-1,"description":"membrane associated ring-CH-type finger 4 [Source:HGNC Symbol;Acc:HGNC:29269]"}, {"versioned_ensembl_gene_id":"ENSG00000238224.1","gene_symbol":"AC104462.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":245614773,"end":245615145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231612.1","gene_symbol":"AC104462.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":245673732,"end":245676478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230504.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824881,"end":29825861,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000181090.20","gene_symbol":"EHMT1","gene_name":"euchromatic histone lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24650]","synonyms":"KMT1D,KIAA1876,FLJ12879,Eu-HMTase1,bA188C12.1","biotype":"protein_coding","ncbi_id":"79813","summary":"The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":137618963,"end":137870016,"strand":1,"description":"euchromatic histone lysine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24650]"}, {"versioned_ensembl_gene_id":"ENSG00000232139.5","gene_symbol":"LINC00867","gene_name":"long intergenic non-protein coding RNA 867 [Source:HGNC Symbol;Acc:HGNC:45265]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506126","summary":null,"start":118357108,"end":118365103,"strand":1,"description":"long intergenic non-protein coding RNA 867 [Source:HGNC Symbol;Acc:HGNC:45265]"}, {"versioned_ensembl_gene_id":"ENSG00000234773.7","gene_symbol":"AC012618.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12195015,"end":12237767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279790.1","gene_symbol":"AL590552.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73971346,"end":73973115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253497.1","gene_symbol":"IGKV1-13","gene_name":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28939","summary":null,"start":89045995,"end":89046466,"strand":-1,"description":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]"}, {"versioned_ensembl_gene_id":"ENSG00000242953.1","gene_symbol":"AC139453.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75395404,"end":75395536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160349.9","gene_symbol":"LCN1","gene_name":"lipocalin 1 [Source:HGNC Symbol;Acc:HGNC:6525]","synonyms":"VEGP,TP,TLC,PMFA,MGC71975","biotype":"protein_coding","ncbi_id":"3933","summary":"This gene encodes a member of the lipocalin family of small secretory proteins. Lipocalins are extracellular transport proteins that bind to a variety of hydrophobic ligands. The encoded protein is the primary lipid binding protein in tears and is overproduced in response to multiple stimuli including infection and stress. The encoded protein may be a marker for chromosome aneuploidy as well as an autoantigen in Sjogren's syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and two pseudogenes of this gene are also located on the long arm of chromosome 9. [provided by RefSeq, Nov 2011]","start":135521438,"end":135526532,"strand":1,"description":"lipocalin 1 [Source:HGNC Symbol;Acc:HGNC:6525]"}, {"versioned_ensembl_gene_id":"ENSG00000274379.1","gene_symbol":"AL121612.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94918253,"end":94918734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240914.1","gene_symbol":"AL121612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94800849,"end":94801463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223572.9","gene_symbol":"CKMT1A","gene_name":"creatine kinase, mitochondrial 1A [Source:HGNC Symbol;Acc:HGNC:31736]","synonyms":"CKMT1","biotype":"protein_coding","ncbi_id":"548596","summary":"Mitochondrial creatine (MtCK) kinase is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine. It belongs to the creatine kinase isoenzyme family. It exists as two isoenzymes, sarcomeric MtCK and ubiquitous MtCK, encoded by separate genes. Mitochondrial creatine kinase occurs in two different oligomeric forms: dimers and octamers, in contrast to the exclusively dimeric cytosolic creatine kinase isoenzymes. Many malignant cancers with poor prognosis have shown overexpression of ubiquitous mitochondrial creatine kinase; this may be related to high energy turnover and failure to eliminate cancer cells via apoptosis. Ubiquitous mitochondrial creatine kinase has 80% homology with the coding exons of sarcomeric mitochondrial creatine kinase. Two genes located near each other on chromosome 15 have been identified which encode identical mitochondrial creatine kinase proteins. [provided by RefSeq, Jul 2008]","start":43692886,"end":43699222,"strand":1,"description":"creatine kinase, mitochondrial 1A [Source:HGNC Symbol;Acc:HGNC:31736]"}, {"versioned_ensembl_gene_id":"ENSG00000235354.1","gene_symbol":"RPS29P16","gene_name":"ribosomal protein S29 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132499","summary":null,"start":103348601,"end":103348771,"strand":1,"description":"ribosomal protein S29 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35560]"}, {"versioned_ensembl_gene_id":"ENSG00000243466.1","gene_symbol":"IGKV1-5","gene_name":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28299","summary":null,"start":88947301,"end":88947957,"strand":-1,"description":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]"}, {"versioned_ensembl_gene_id":"ENSG00000137727.12","gene_symbol":"ARHGAP20","gene_name":"Rho GTPase activating protein 20 [Source:HGNC Symbol;Acc:HGNC:18357]","synonyms":"KIAA1391","biotype":"protein_coding","ncbi_id":"57569","summary":"The protein encoded by this gene is an activator of RHO-type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth. [provided by RefSeq, Sep 2016]","start":110577042,"end":110713189,"strand":-1,"description":"Rho GTPase activating protein 20 [Source:HGNC Symbol;Acc:HGNC:18357]"}, {"versioned_ensembl_gene_id":"ENSG00000154227.13","gene_symbol":"CERS3","gene_name":"ceramide synthase 3 [Source:HGNC Symbol;Acc:HGNC:23752]","synonyms":"MGC27091,LASS3","biotype":"protein_coding","ncbi_id":"204219","summary":"This gene is a member of the ceramide synthase family of genes. The ceramide synthase enzymes regulate sphingolipid synthesis by catalyzing the formation of ceramides from sphingoid base and acyl-coA substrates. This family member is involved in the synthesis of ceramides with ultra-long-chain acyl moieties (ULC-Cers), important to the epidermis in its role in creating a protective barrier from the environment. The protein encoded by this gene has also been implicated in modification of the lipid structures required for spermatogenesis. Mutations in this gene have been associated with male fertility defects, and epidermal defects, including ichthyosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":100400395,"end":100544995,"strand":-1,"description":"ceramide synthase 3 [Source:HGNC Symbol;Acc:HGNC:23752]"}, {"versioned_ensembl_gene_id":"ENSG00000225136.1","gene_symbol":"PGBD4P5","gene_name":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421123","summary":null,"start":88922328,"end":88922753,"strand":-1,"description":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]"}, {"versioned_ensembl_gene_id":"ENSG00000197794.2","gene_symbol":"IGKV7-3","gene_name":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28905","summary":null,"start":88915081,"end":88915378,"strand":-1,"description":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]"}, {"versioned_ensembl_gene_id":"ENSG00000259887.1","gene_symbol":"AC068987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51848223,"end":51852729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113520.10","gene_symbol":"IL4","gene_name":"interleukin 4 [Source:HGNC Symbol;Acc:HGNC:6014]","synonyms":"BSF1,BCGF1,BCGF-1,MGC79402,IL-4","biotype":"protein_coding","ncbi_id":"3565","summary":"The protein encoded by this gene is a pleiotropic cytokine produced by activated T cells. This cytokine is a ligand for interleukin 4 receptor. The interleukin 4 receptor also binds to IL13, which may contribute to many overlapping functions of this cytokine and IL13. STAT6, a signal transducer and activator of transcription, has been shown to play a central role in mediating the immune regulatory signal of this cytokine. This gene, IL3, IL5, IL13, and CSF2 form a cytokine gene cluster on chromosome 5q, with this gene particularly close to IL13. This gene, IL13 and IL5 are found to be regulated coordinately by several long-range regulatory elements in an over 120 kilobase range on the chromosome. IL4 is considered an important cytokine for tissue repair, counterbalancing the effects of proinflammatory type 1 cytokines, however, it also promotes allergic airway inflammation. Moreover, IL-4, a type 2 cytokine, mediates and regulates a variety of human host responses such as allergic, anti-parasitic, wound healing, and acute inflammation. This cytokine has been reported to promote resolution of neutrophil-mediated acute lung injury. In an allergic response, IL-4 has an essential role in the production of allergen-specific immunoglobin (Ig) E. This pro-inflammatory cytokine has been observed to be increased in COVID-19 (Coronavirus disease 2019) patients, but is not necessarily associated with severe COVID-19 pathology. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Aug 2020]","start":132673986,"end":132682676,"strand":1,"description":"interleukin 4 [Source:HGNC Symbol;Acc:HGNC:6014]"}, {"versioned_ensembl_gene_id":"ENSG00000250886.1","gene_symbol":"AC010368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35081223,"end":35081992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163347.5","gene_symbol":"CLDN1","gene_name":"claudin 1 [Source:HGNC Symbol;Acc:HGNC:2032]","synonyms":"SEMP1,ILVASC","biotype":"protein_coding","ncbi_id":"9076","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome. [provided by RefSeq, Jul 2008]","start":190305701,"end":190322475,"strand":-1,"description":"claudin 1 [Source:HGNC Symbol;Acc:HGNC:2032]"}, {"versioned_ensembl_gene_id":"ENSG00000070081.15","gene_symbol":"NUCB2","gene_name":"nucleobindin 2 [Source:HGNC Symbol;Acc:HGNC:8044]","synonyms":"NEFA","biotype":"protein_coding","ncbi_id":"4925","summary":"This gene encodes a protein with a suggested role in calcium level maintenance, eating regulation in the hypothalamus, and release of tumor necrosis factor from vascular endothelial cells. This protein binds calcium and has EF-folding domains. [provided by RefSeq, Oct 2011]","start":17208153,"end":17349974,"strand":1,"description":"nucleobindin 2 [Source:HGNC Symbol;Acc:HGNC:8044]"}, {"versioned_ensembl_gene_id":"ENSG00000187747.2","gene_symbol":"OR52B6","gene_name":"olfactory receptor family 52 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:15211]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340980","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5580877,"end":5581884,"strand":1,"description":"olfactory receptor family 52 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:15211]"}, {"versioned_ensembl_gene_id":"ENSG00000225531.1","gene_symbol":"AL807761.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107116829,"end":107117557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226047.1","gene_symbol":"AL807761.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107117459,"end":107121705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234604.2","gene_symbol":"AL021068.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169474060,"end":169474159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269307.1","gene_symbol":"AC010463.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17267418,"end":17282966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118242.15","gene_symbol":"MREG","gene_name":"melanoregulin [Source:HGNC Symbol;Acc:HGNC:25478]","synonyms":"WDT2,FLJ10116,DSU","biotype":"protein_coding","ncbi_id":"55686","summary":null,"start":215942805,"end":216034096,"strand":-1,"description":"melanoregulin [Source:HGNC Symbol;Acc:HGNC:25478]"}, {"versioned_ensembl_gene_id":"ENSG00000237937.5","gene_symbol":"AP000770.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116639422,"end":116658252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281183.1","gene_symbol":"NPTN-IT1","gene_name":"NPTN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:45091]","synonyms":"lncRNA-LET","biotype":"sense_intronic","ncbi_id":"101241892","summary":null,"start":73567012,"end":73569294,"strand":-1,"description":"NPTN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:45091]"}, {"versioned_ensembl_gene_id":"ENSG00000115425.13","gene_symbol":"PECR","gene_name":"peroxisomal trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:18281]","synonyms":"TERP,SDR29C1,HSA250303","biotype":"protein_coding","ncbi_id":"55825","summary":null,"start":215996329,"end":216082955,"strand":-1,"description":"peroxisomal trans-2-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:18281]"}, {"versioned_ensembl_gene_id":"ENSG00000260254.1","gene_symbol":"AP000997.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115638563,"end":115646962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060971.17","gene_symbol":"ACAA1","gene_name":"acetyl-CoA acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:82]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30","summary":"This gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":38103129,"end":38137242,"strand":-1,"description":"acetyl-CoA acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:82]"}, {"versioned_ensembl_gene_id":"ENSG00000085511.19","gene_symbol":"MAP3K4","gene_name":"mitogen-activated protein kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6856]","synonyms":"MTK1,MEKK4,MAPKKK4,KIAA0213","biotype":"protein_coding","ncbi_id":"4216","summary":"The central core of each mitogen-activated protein kinase (MAPK) pathway is a conserved cascade of 3 protein kinases: an activated MAPK kinase kinase (MAPKKK) phosphorylates and activates a specific MAPK kinase (MAPKK), which then activates a specific MAPK. While the ERK MAPKs are activated by mitogenic stimulation, the CSBP2 and JNK MAPKs are activated by environmental stresses such as osmotic shock, UV irradiation, wound stress, and inflammatory factors. This gene encodes a MAPKKK, the MEKK4 protein, also called MTK1. This protein contains a protein kinase catalytic domain at the C terminus. The N-terminal nonkinase domain may contain a regulatory domain. Expression of MEKK4 in mammalian cells activated the CSBP2 and JNK MAPK pathways, but not the ERK pathway. In vitro kinase studies indicated that recombinant MEKK4 can specifically phosphorylate and activate PRKMK6 and SERK1, MAPKKs that activate CSBP2 and JNK, respectively but cannot phosphorylate PRKMK1, an MAPKK that activates ERKs. MEKK4 is a major mediator of environmental stresses that activate the CSBP2 MAPK pathway, and a minor mediator of the JNK pathway. Several alternatively spliced transcripts encoding distinct isoforms have been described. [provided by RefSeq, May 2014]","start":160991727,"end":161117385,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6856]"}, {"versioned_ensembl_gene_id":"ENSG00000124459.11","gene_symbol":"ZNF45","gene_name":"zinc finger protein 45 [Source:HGNC Symbol;Acc:HGNC:13111]","synonyms":"ZNF13","biotype":"protein_coding","ncbi_id":"7596","summary":null,"start":43912629,"end":43935278,"strand":-1,"description":"zinc finger protein 45 [Source:HGNC Symbol;Acc:HGNC:13111]"}, {"versioned_ensembl_gene_id":"ENSG00000164300.16","gene_symbol":"SERINC5","gene_name":"serine incorporator 5 [Source:HGNC Symbol;Acc:HGNC:18825]","synonyms":"TPO1,C5orf12","biotype":"protein_coding","ncbi_id":"256987","summary":null,"start":80111651,"end":80256079,"strand":-1,"description":"serine incorporator 5 [Source:HGNC Symbol;Acc:HGNC:18825]"}, {"versioned_ensembl_gene_id":"ENSG00000120327.6","gene_symbol":"PCDHB14","gene_name":"protocadherin beta 14 [Source:HGNC Symbol;Acc:HGNC:8685]","synonyms":"PCDH-BETA14","biotype":"protein_coding","ncbi_id":"56122","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141222932,"end":141227759,"strand":1,"description":"protocadherin beta 14 [Source:HGNC Symbol;Acc:HGNC:8685]"}, {"versioned_ensembl_gene_id":"ENSG00000230026.2","gene_symbol":"AL357556.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235361153,"end":235362540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255555.1","gene_symbol":"AP000857.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84936689,"end":84955705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254787.1","gene_symbol":"AP001825.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84720826,"end":84800701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255689.1","gene_symbol":"AP003174.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115582297,"end":115600339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125454.11","gene_symbol":"SLC25A19","gene_name":"solute carrier family 25 member 19 [Source:HGNC Symbol;Acc:HGNC:14409]","synonyms":"TPC,MUP1,MCPHA,DNC","biotype":"protein_coding","ncbi_id":"60386","summary":"This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":75272981,"end":75289510,"strand":-1,"description":"solute carrier family 25 member 19 [Source:HGNC Symbol;Acc:HGNC:14409]"}, {"versioned_ensembl_gene_id":"ENSG00000269729.1","gene_symbol":"AC006262.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46163893,"end":46180647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268621.5","gene_symbol":"IGFL2-AS1","gene_name":"IGFL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52559]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645553","summary":null,"start":46189166,"end":46203083,"strand":-1,"description":"IGFL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52559]"}, {"versioned_ensembl_gene_id":"ENSG00000242970.2","gene_symbol":"AC068522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58588420,"end":58588764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235541.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969118,"end":28970448,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000279935.1","gene_symbol":"AL353611.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134992958,"end":134995854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258203.5","gene_symbol":"AC004801.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48005277,"end":48011227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146006.7","gene_symbol":"LRRTM2","gene_name":"leucine rich repeat transmembrane neuronal 2 [Source:HGNC Symbol;Acc:HGNC:19409]","synonyms":"KIAA0416","biotype":"protein_coding","ncbi_id":"26045","summary":null,"start":138868923,"end":138875368,"strand":-1,"description":"leucine rich repeat transmembrane neuronal 2 [Source:HGNC Symbol;Acc:HGNC:19409]"}, {"versioned_ensembl_gene_id":"ENSG00000188425.3","gene_symbol":"NANOS2","gene_name":"nanos C2HC-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23292]","synonyms":"ZC2HC12B,NOS2","biotype":"protein_coding","ncbi_id":"339345","summary":null,"start":45913214,"end":45914870,"strand":-1,"description":"nanos C2HC-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23292]"}, {"versioned_ensembl_gene_id":"ENSG00000170604.4","gene_symbol":"IRF2BP1","gene_name":"interferon regulatory factor 2 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21728]","synonyms":"DKFZP434M154,IRF-2BP1","biotype":"protein_coding","ncbi_id":"26145","summary":null,"start":45883607,"end":45886170,"strand":-1,"description":"interferon regulatory factor 2 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21728]"}, {"versioned_ensembl_gene_id":"ENSG00000268204.1","gene_symbol":"AC008763.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7633766,"end":7636990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141756.18","gene_symbol":"FKBP10","gene_name":"FK506 binding protein 10 [Source:HGNC Symbol;Acc:HGNC:18169]","synonyms":"hFKBP65,FLJ23833,FLJ22041,FLJ20683,FKBP6","biotype":"protein_coding","ncbi_id":"60681","summary":"The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This protein localizes to the endoplasmic reticulum and acts as a molecular chaperone. Alternatively spliced variants encoding different isoforms have been reported, but their biological validity has not been determined.[provided by RefSeq, Nov 2009]","start":41812680,"end":41823217,"strand":1,"description":"FK506 binding protein 10 [Source:HGNC Symbol;Acc:HGNC:18169]"}, {"versioned_ensembl_gene_id":"ENSG00000042304.11","gene_symbol":"C2orf83","gene_name":"chromosome 2 open reading frame 83 [Source:HGNC Symbol;Acc:HGNC:25344]","synonyms":"DKFZp547H025","biotype":"protein_coding","ncbi_id":"56918","summary":null,"start":227610090,"end":227648606,"strand":-1,"description":"chromosome 2 open reading frame 83 [Source:HGNC Symbol;Acc:HGNC:25344]"}, {"versioned_ensembl_gene_id":"ENSG00000279825.1","gene_symbol":"AC003957.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19030857,"end":19033529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269800.1","gene_symbol":"PLEKHA3P1","gene_name":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]","synonyms":"PLEKHA3P","biotype":"processed_pseudogene","ncbi_id":"91405","summary":null,"start":41521043,"end":41521989,"strand":-1,"description":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]"}, {"versioned_ensembl_gene_id":"ENSG00000188522.14","gene_symbol":"FAM83G","gene_name":"family with sequence similarity 83 member G [Source:HGNC Symbol;Acc:HGNC:32554]","synonyms":"PAWS1,FLJ41564","biotype":"protein_coding","ncbi_id":"644815","summary":null,"start":18968789,"end":19004804,"strand":-1,"description":"family with sequence similarity 83 member G [Source:HGNC Symbol;Acc:HGNC:32554]"}, {"versioned_ensembl_gene_id":"ENSG00000274933.5","gene_symbol":"TBC1D3I","gene_name":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724862","summary":null,"start":36253456,"end":36264553,"strand":-1,"description":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]"}, {"versioned_ensembl_gene_id":"ENSG00000196666.4","gene_symbol":"FAM180B","gene_name":"family with sequence similarity 180 member B [Source:HGNC Symbol;Acc:HGNC:34451]","synonyms":"LOC399888","biotype":"protein_coding","ncbi_id":"399888","summary":null,"start":47586693,"end":47589194,"strand":1,"description":"family with sequence similarity 180 member B [Source:HGNC Symbol;Acc:HGNC:34451]"}, {"versioned_ensembl_gene_id":"ENSG00000249715.11","gene_symbol":"FER1L5","gene_name":"fer-1 like family member 5 [Source:HGNC Symbol;Acc:HGNC:19044]","synonyms":"DKFZp434I0121","biotype":"protein_coding","ncbi_id":"90342","summary":null,"start":96642737,"end":96704887,"strand":1,"description":"fer-1 like family member 5 [Source:HGNC Symbol;Acc:HGNC:19044]"}, {"versioned_ensembl_gene_id":"ENSG00000251366.1","gene_symbol":"DBIP2","gene_name":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2691]","synonyms":"DBIL1","biotype":"processed_pseudogene","ncbi_id":"1623","summary":null,"start":80603383,"end":80603644,"strand":-1,"description":"diazepam binding inhibitor, acyl-CoA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2691]"}, {"versioned_ensembl_gene_id":"ENSG00000278395.1","gene_symbol":"AC243829.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36241701,"end":36241806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278097.1","gene_symbol":"AC243829.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36225246,"end":36226807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253665.1","gene_symbol":"AC022733.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40114651,"end":40127468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103356.15","gene_symbol":"EARS2","gene_name":"glutamyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29419]","synonyms":"MSE1,KIAA1970","biotype":"protein_coding","ncbi_id":"124454","summary":"This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of glutamate to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 12 (COXPD12). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":23522014,"end":23557731,"strand":-1,"description":"glutamyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29419]"}, {"versioned_ensembl_gene_id":"ENSG00000124098.9","gene_symbol":"FAM210B","gene_name":"family with sequence similarity 210 member B [Source:HGNC Symbol;Acc:HGNC:16102]","synonyms":"DKFZP434A1114,dJ1167H4.1,C20orf108","biotype":"protein_coding","ncbi_id":"116151","summary":null,"start":56358915,"end":56368663,"strand":1,"description":"family with sequence similarity 210 member B [Source:HGNC Symbol;Acc:HGNC:16102]"}, {"versioned_ensembl_gene_id":"ENSG00000114982.17","gene_symbol":"KANSL3","gene_name":"KAT8 regulatory NSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25473]","synonyms":"Rcd1,NSL3,KIAA1310,FLJ10081","biotype":"protein_coding","ncbi_id":"55683","summary":null,"start":96593170,"end":96642787,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25473]"}, {"versioned_ensembl_gene_id":"ENSG00000253839.1","gene_symbol":"AC013546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136489448,"end":136529876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061455.10","gene_symbol":"PRDM6","gene_name":"PR/SET domain 6 [Source:HGNC Symbol;Acc:HGNC:9350]","synonyms":"PRISM,KMT8C","biotype":"protein_coding","ncbi_id":"93166","summary":"The protein encoded by this gene is a transcriptional repressor and a member of the PRDM family. Family members contain a PR domain and multiple zinc-finger domains. The encoded protein is involved in regulation of vascular smooth muscle cells (VSMC) contractile proteins. Mutations in this gene result in patent ductus arteriosus 3 (PDA3). [provided by RefSeq, Apr 2017]","start":123089121,"end":123194266,"strand":1,"description":"PR/SET domain 6 [Source:HGNC Symbol;Acc:HGNC:9350]"}, {"versioned_ensembl_gene_id":"ENSG00000276434.1","gene_symbol":"AL136221.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113339450,"end":113339958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233581.1","gene_symbol":"AC069155.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216303325,"end":216321737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230843.1","gene_symbol":"AL139824.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56295967,"end":56299160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234750.1","gene_symbol":"AC012618.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12284337,"end":12285185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260804.3","gene_symbol":"LINC01963","gene_name":"long intergenic non-protein coding RNA 1963 [Source:HGNC Symbol;Acc:HGNC:25283]","synonyms":"DKFZp434H1419","biotype":"lincRNA","ncbi_id":"150967","summary":null,"start":216217045,"end":216220192,"strand":1,"description":"long intergenic non-protein coding RNA 1963 [Source:HGNC Symbol;Acc:HGNC:25283]"}, {"versioned_ensembl_gene_id":"ENSG00000274563.1","gene_symbol":"GU182343.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54766539,"end":54781397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186834.3","gene_symbol":"HEXIM1","gene_name":"hexamethylene bisacetamide inducible 1 [Source:HGNC Symbol;Acc:HGNC:24953]","synonyms":"MAQ1,HIS1,EDG1,CLP-1","biotype":"protein_coding","ncbi_id":"10614","summary":"Expression of this gene is induced by hexamethylene-bis-acetamide in vascular smooth muscle cells. This gene has no introns. [provided by RefSeq, Jul 2008]","start":45148502,"end":45152101,"strand":1,"description":"hexamethylene bisacetamide inducible 1 [Source:HGNC Symbol;Acc:HGNC:24953]"}, {"versioned_ensembl_gene_id":"ENSG00000272102.1","gene_symbol":"AL133406.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105273220,"end":105273760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249290.5","gene_symbol":"AC010181.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140449435,"end":140460351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248991.1","gene_symbol":"AC097375.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151919468,"end":151943933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232895.2","gene_symbol":"AL121999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114206427,"end":114262278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253957.1","gene_symbol":"IGHV3-22","gene_name":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28443","summary":null,"start":106257762,"end":106258223,"strand":-1,"description":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]"}, {"versioned_ensembl_gene_id":"ENSG00000211923.1","gene_symbol":"IGHD3-10","gene_name":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]","synonyms":"DXP'1,IGHD310","biotype":"IG_D_gene","ncbi_id":"28499","summary":null,"start":105904497,"end":105904527,"strand":-1,"description":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]"}, {"versioned_ensembl_gene_id":"ENSG00000160336.14","gene_symbol":"ZNF761","gene_name":"zinc finger protein 761 [Source:HGNC Symbol;Acc:HGNC:23179]","synonyms":"KIAA2033,FLJ35333,FLJ16231","biotype":"protein_coding","ncbi_id":"388561","summary":null,"start":53431993,"end":53458261,"strand":1,"description":"zinc finger protein 761 [Source:HGNC Symbol;Acc:HGNC:23179]"}, {"versioned_ensembl_gene_id":"ENSG00000167004.12","gene_symbol":"PDIA3","gene_name":"protein disulfide isomerase family A member 3 [Source:HGNC Symbol;Acc:HGNC:4606]","synonyms":"PI-PLC,P58,HsT17083,GRP58,GRP57,ERp61,ERp60,ERp57","biotype":"protein_coding","ncbi_id":"2923","summary":"This gene encodes a protein of the endoplasmic reticulum that interacts with lectin chaperones calreticulin and calnexin to modulate folding of newly synthesized glycoproteins. The protein was once thought to be a phospholipase; however, it has been demonstrated that the protein actually has protein disulfide isomerase activity. It is thought that complexes of lectins and this protein mediate protein folding by promoting formation of disulfide bonds in their glycoprotein substrates. This protein also functions as a molecular chaperone that prevents the formation of protein aggregates. [provided by RefSeq, Dec 2016]","start":43746392,"end":43773279,"strand":1,"description":"protein disulfide isomerase family A member 3 [Source:HGNC Symbol;Acc:HGNC:4606]"}, {"versioned_ensembl_gene_id":"ENSG00000211947.2","gene_symbol":"IGHV3-21","gene_name":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28444","summary":null,"start":106235064,"end":106235594,"strand":-1,"description":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]"}, {"versioned_ensembl_gene_id":"ENSG00000249906.1","gene_symbol":"AC006487.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49505657,"end":49574064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180219.1","gene_symbol":"FAM71C","gene_name":"family with sequence similarity 71 member C [Source:HGNC Symbol;Acc:HGNC:28594]","synonyms":"MGC39520","biotype":"protein_coding","ncbi_id":"196472","summary":null,"start":99647753,"end":99650046,"strand":1,"description":"family with sequence similarity 71 member C [Source:HGNC Symbol;Acc:HGNC:28594]"}, {"versioned_ensembl_gene_id":"ENSG00000205771.6","gene_symbol":"CATSPER2P1","gene_name":"cation channel sperm associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31054]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440278","summary":"Catsper genes belong to a family of putative cation channels that are specific to spermatozoa and localize to the flagellum. This gene is part of a tandem repeat on chromosome 15q15; this copy of the gene is thought to be a pseudogene. [provided by RefSeq, Oct 2008]","start":43726918,"end":43747094,"strand":-1,"description":"cation channel sperm associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31054]"}, {"versioned_ensembl_gene_id":"ENSG00000230048.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"NG37,G7c,C6orf27","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31747771,"end":31759475,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000064300.8","gene_symbol":"NGFR","gene_name":"nerve growth factor receptor [Source:HGNC Symbol;Acc:HGNC:7809]","synonyms":"TNFRSF16,p75NTR,CD271","biotype":"protein_coding","ncbi_id":"4804","summary":"Nerve growth factor receptor contains an extracellular domain containing four 40-amino acid repeats with 6 cysteine residues at conserved positions followed by a serine/threonine-rich region, a single transmembrane domain, and a 155-amino acid cytoplasmic domain. The cysteine-rich region contains the nerve growth factor binding domain. [provided by RefSeq, Jul 2008]","start":49495293,"end":49515017,"strand":1,"description":"nerve growth factor receptor [Source:HGNC Symbol;Acc:HGNC:7809]"}, {"versioned_ensembl_gene_id":"ENSG00000163518.10","gene_symbol":"FCRL4","gene_name":"Fc receptor like 4 [Source:HGNC Symbol;Acc:HGNC:18507]","synonyms":"IRTA1,IGFP2,FCRH4,CD307d","biotype":"protein_coding","ncbi_id":"83417","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein has four extracellular C2-type immunoglobulin domains, a transmembrane domain and a cytoplasmic domain that contains three immune-receptor tyrosine-based inhibitory motifs. This protein may play a role in the function of memory B-cells in the epithelia. Aberrations in the chromosomal region encoding this gene are associated with non-Hodgkin lymphoma and multiple myeloma. [provided by RefSeq, Apr 2009]","start":157573749,"end":157598080,"strand":-1,"description":"Fc receptor like 4 [Source:HGNC Symbol;Acc:HGNC:18507]"}, {"versioned_ensembl_gene_id":"ENSG00000171357.5","gene_symbol":"LURAP1","gene_name":"leucine rich adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:32327]","synonyms":"LRAP35a,FLJ25163,C1orf190","biotype":"protein_coding","ncbi_id":"541468","summary":null,"start":46203334,"end":46221261,"strand":1,"description":"leucine rich adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:32327]"}, {"versioned_ensembl_gene_id":"ENSG00000245261.1","gene_symbol":"AL133375.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43213801,"end":43223860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132740.8","gene_symbol":"IGHMBP2","gene_name":"immunoglobulin mu binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5542]","synonyms":"HMN6,HCSA,CMT2S,CATF1,ZFAND7,SMUBP2,SMARD1","biotype":"protein_coding","ncbi_id":"3508","summary":"This gene encodes a helicase superfamily member that binds a specific DNA sequence from the immunoglobulin mu chain switch region. Mutations in this gene lead to spinal muscle atrophy with respiratory distress type 1. [provided by RefSeq, Jul 2008]","start":68903842,"end":68940602,"strand":1,"description":"immunoglobulin mu binding protein 2 [Source:HGNC Symbol;Acc:HGNC:5542]"}, {"versioned_ensembl_gene_id":"ENSG00000225129.1","gene_symbol":"AL035250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59352195,"end":59357774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147099.19","gene_symbol":"HDAC8","gene_name":"histone deacetylase 8 [Source:HGNC Symbol;Acc:HGNC:13315]","synonyms":"WTS,RPD3,MRXS6,HDACL1","biotype":"protein_coding","ncbi_id":"55869","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class I of the histone deacetylase family. It catalyzes the deacetylation of lysine residues in the histone N-terminal tails and represses transcription in large multiprotein complexes with transcriptional co-repressors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":72329516,"end":72573103,"strand":-1,"description":"histone deacetylase 8 [Source:HGNC Symbol;Acc:HGNC:13315]"}, {"versioned_ensembl_gene_id":"ENSG00000172350.9","gene_symbol":"ABCG4","gene_name":"ATP binding cassette subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:13884]","synonyms":"WHITE2","biotype":"protein_coding","ncbi_id":"64137","summary":"The protein encoded by this gene is a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). The encoded protein is a member of the White subfamily and plays an important role in cellular cholesterol homeostasis. This protein functions as either a homodimer or as a heterodimer with another ABC subfamily protein such as ABCG1. [provided by RefSeq, Jan 2017]","start":119149012,"end":119162653,"strand":1,"description":"ATP binding cassette subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:13884]"}, {"versioned_ensembl_gene_id":"ENSG00000164402.13","gene_symbol":"SEPT8","gene_name":"septin 8 [Source:HGNC Symbol;Acc:HGNC:16511]","synonyms":"SEP2,KIAA0202","biotype":"protein_coding","ncbi_id":"23176","summary":"This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":132750817,"end":132807241,"strand":-1,"description":"septin 8 [Source:HGNC Symbol;Acc:HGNC:16511]"}, {"versioned_ensembl_gene_id":"ENSG00000085871.8","gene_symbol":"MGST2","gene_name":"microsomal glutathione S-transferase 2 [Source:HGNC Symbol;Acc:HGNC:7063]","synonyms":"MGST-II","biotype":"protein_coding","ncbi_id":"4258","summary":"The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family consists of six human proteins, several of which are involved in the production of leukotrienes and prostaglandin E, important mediators of inflammation. This gene encodes a protein which catalyzes the conjugation of leukotriene A4 and reduced glutathione to produce leukotriene C4. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2011]","start":139665768,"end":139740745,"strand":1,"description":"microsomal glutathione S-transferase 2 [Source:HGNC Symbol;Acc:HGNC:7063]"}, {"versioned_ensembl_gene_id":"ENSG00000211918.1","gene_symbol":"IGHD2-15","gene_name":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]","synonyms":"IGHD215,D2","biotype":"IG_D_gene","ncbi_id":"28503","summary":null,"start":105897957,"end":105897987,"strand":-1,"description":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]"}, {"versioned_ensembl_gene_id":"ENSG00000276044.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54833799,"end":54844782,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000254048.1","gene_symbol":"AC105150.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58991720,"end":58992938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227326.2","gene_symbol":"BX005428.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800695,"end":29801491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085998.13","gene_symbol":"POMGNT1","gene_name":"protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Source:HGNC Symbol;Acc:HGNC:19139]","synonyms":"MGAT1.2,MEB,LGMD2O,FLJ20277","biotype":"protein_coding","ncbi_id":"55624","summary":"This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":46188682,"end":46220305,"strand":-1,"description":"protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Source:HGNC Symbol;Acc:HGNC:19139]"}, {"versioned_ensembl_gene_id":"ENSG00000124780.13","gene_symbol":"KCNK17","gene_name":"potassium two pore domain channel subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:14465]","synonyms":"TALK-2,K2p17.1,TASK4,TASK-4,TALK2","biotype":"protein_coding","ncbi_id":"89822","summary":"The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is activated at alkaline pH. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":39299001,"end":39314553,"strand":-1,"description":"potassium two pore domain channel subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:14465]"}, {"versioned_ensembl_gene_id":"ENSG00000100697.14","gene_symbol":"DICER1","gene_name":"dicer 1, ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17098]","synonyms":"MNG1,KIAA0928,K12H4.8-LIKE,HERNA,Dicer","biotype":"protein_coding","ncbi_id":"23405","summary":"This gene encodes a protein possessing an RNA helicase motif containing a DEXH box in its amino terminus and an RNA motif in the carboxy terminus. The encoded protein functions as a ribonuclease and is required by the RNA interference and small temporal RNA (stRNA) pathways to produce the active small RNA component that represses gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":95086228,"end":95158010,"strand":-1,"description":"dicer 1, ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17098]"}, {"versioned_ensembl_gene_id":"ENSG00000260221.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797915,"end":29799945,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000149179.13","gene_symbol":"C11orf49","gene_name":"chromosome 11 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28720]","synonyms":"MGC4707,FLJ22210","biotype":"protein_coding","ncbi_id":"79096","summary":null,"start":46936689,"end":47164385,"strand":1,"description":"chromosome 11 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28720]"}, {"versioned_ensembl_gene_id":"ENSG00000139890.9","gene_symbol":"REM2","gene_name":"RRAD and GEM like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:20248]","synonyms":"FLJ38964","biotype":"protein_coding","ncbi_id":"161253","summary":null,"start":22883165,"end":22887686,"strand":1,"description":"RRAD and GEM like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:20248]"}, {"versioned_ensembl_gene_id":"ENSG00000100292.16","gene_symbol":"HMOX1","gene_name":"heme oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:5013]","synonyms":"HO-1,bK286B10","biotype":"protein_coding","ncbi_id":"3162","summary":"Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. [provided by RefSeq, Jul 2008]","start":35380361,"end":35394214,"strand":1,"description":"heme oxygenase 1 [Source:HGNC Symbol;Acc:HGNC:5013]"}, {"versioned_ensembl_gene_id":"ENSG00000282041.1","gene_symbol":"Z82244.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35376422,"end":35377261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116350.16","gene_symbol":"SRSF4","gene_name":"serine and arginine rich splicing factor 4 [Source:HGNC Symbol;Acc:HGNC:10786]","synonyms":"SRP75,SFRS4","biotype":"protein_coding","ncbi_id":"6429","summary":"This gene encodes a member of the arginine/serine-rich splicing factor family. The encoded protein likely functions in mRNA processing. [provided by RefSeq, Feb 2009]","start":29147743,"end":29181987,"strand":-1,"description":"serine and arginine rich splicing factor 4 [Source:HGNC Symbol;Acc:HGNC:10786]"}, {"versioned_ensembl_gene_id":"ENSG00000111450.13","gene_symbol":"STX2","gene_name":"syntaxin 2 [Source:HGNC Symbol;Acc:HGNC:3403]","synonyms":"STX2C,STX2B,STX2A,EPM,EPIM","biotype":"protein_coding","ncbi_id":"2054","summary":"The product of this gene belongs to the syntaxin/epimorphin family of proteins. The syntaxins are a large protein family implicated in the targeting and fusion of intracellular transport vesicles. The product of this gene regulates epithelial-mesenchymal interactions and epithelial cell morphogenesis and activation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":130789600,"end":130839266,"strand":-1,"description":"syntaxin 2 [Source:HGNC Symbol;Acc:HGNC:3403]"}, {"versioned_ensembl_gene_id":"ENSG00000157426.13","gene_symbol":"AASDH","gene_name":"aminoadipate-semialdehyde dehydrogenase [Source:HGNC Symbol;Acc:HGNC:23993]","synonyms":"NRPS998,LYS2,ACSF4","biotype":"protein_coding","ncbi_id":"132949","summary":"This gene encodes a member of the non-ribosome peptide syntesase (NRPS) enzyme family. The encoded protein contains an AMP-binding domain, PP-binding (phosphopantetheine, or pantetheine 4'phosphate-binding) domain and the Pyrrolo-quinoline quinon (PQQ) binding domain. The protein is expressed in several adult tissues. [provided by RefSeq, Apr 2016]","start":56338287,"end":56387508,"strand":-1,"description":"aminoadipate-semialdehyde dehydrogenase [Source:HGNC Symbol;Acc:HGNC:23993]"}, {"versioned_ensembl_gene_id":"ENSG00000147400.8","gene_symbol":"CETN2","gene_name":"centrin 2 [Source:HGNC Symbol;Acc:HGNC:1867]","synonyms":"CEN2,CALT","biotype":"protein_coding","ncbi_id":"1069","summary":" Caltractin belongs to a family of calcium-binding proteins and is a structural component of the centrosome. The high level of conservation from algae to humans and its association with the centrosome suggested that caltractin plays a fundamental role in the structure and function of the microtubule-organizing center, possibly required for the proper duplication and segregation of the centrosome. [provided by RefSeq, Jul 2008]","start":152826973,"end":152830777,"strand":-1,"description":"centrin 2 [Source:HGNC Symbol;Acc:HGNC:1867]"}, {"versioned_ensembl_gene_id":"ENSG00000148935.10","gene_symbol":"GAS2","gene_name":"growth arrest specific 2 [Source:HGNC Symbol;Acc:HGNC:4167]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2620","summary":"The protein encoded by this gene is a caspase-3 substrate that plays a role in regulating microfilament and cell shape changes during apoptosis. It can also modulate cell susceptibility to p53-dependent apoptosis by inhibiting calpain activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2017]","start":22625642,"end":22813055,"strand":1,"description":"growth arrest specific 2 [Source:HGNC Symbol;Acc:HGNC:4167]"}, {"versioned_ensembl_gene_id":"ENSG00000112419.14","gene_symbol":"PHACTR2","gene_name":"phosphatase and actin regulator 2 [Source:HGNC Symbol;Acc:HGNC:20956]","synonyms":"KIAA0680,C6orf56","biotype":"protein_coding","ncbi_id":"9749","summary":null,"start":143536845,"end":143831185,"strand":1,"description":"phosphatase and actin regulator 2 [Source:HGNC Symbol;Acc:HGNC:20956]"}, {"versioned_ensembl_gene_id":"ENSG00000126261.12","gene_symbol":"UBA2","gene_name":"ubiquitin like modifier activating enzyme 2 [Source:HGNC Symbol;Acc:HGNC:30661]","synonyms":"SAE2,HRIHFB2115,FLJ13058,ARX","biotype":"protein_coding","ncbi_id":"10054","summary":"Posttranslational modification of proteins by the addition of the small protein SUMO (see SUMO1; MIM 601912), or sumoylation, regulates protein structure and intracellular localization. SAE1 (MIM 613294) and UBA2 form a heterodimer that functions as a SUMO-activating enzyme for the sumoylation of proteins (Okuma et al., 1999 [PubMed 9920803]).[supplied by OMIM, Mar 2010]","start":34428352,"end":34471251,"strand":1,"description":"ubiquitin like modifier activating enzyme 2 [Source:HGNC Symbol;Acc:HGNC:30661]"}, {"versioned_ensembl_gene_id":"ENSG00000135521.8","gene_symbol":"LTV1","gene_name":"LTV1 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:21173]","synonyms":"FLJ14909,dJ468K18.4,C6orf93","biotype":"protein_coding","ncbi_id":"84946","summary":null,"start":143843344,"end":143863812,"strand":1,"description":"LTV1 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:21173]"}, {"versioned_ensembl_gene_id":"ENSG00000235166.7","gene_symbol":"LINC01440","gene_name":"long intergenic non-protein coding RNA 1440 [Source:HGNC Symbol;Acc:HGNC:50762]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723578","summary":null,"start":55408898,"end":55482777,"strand":1,"description":"long intergenic non-protein coding RNA 1440 [Source:HGNC Symbol;Acc:HGNC:50762]"}, {"versioned_ensembl_gene_id":"ENSG00000185896.10","gene_symbol":"LAMP1","gene_name":"lysosomal associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6499]","synonyms":"CD107a","biotype":"protein_coding","ncbi_id":"3916","summary":"The protein encoded by this gene is a member of a family of membrane glycoproteins. This glycoprotein provides selectins with carbohydrate ligands. It may also play a role in tumor cell metastasis. [provided by RefSeq, Jul 2008]","start":113297241,"end":113323672,"strand":1,"description":"lysosomal associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6499]"}, {"versioned_ensembl_gene_id":"ENSG00000140025.15","gene_symbol":"EFCAB11","gene_name":"EF-hand calcium binding domain 11 [Source:HGNC Symbol;Acc:HGNC:20357]","synonyms":"C14orf143","biotype":"protein_coding","ncbi_id":"90141","summary":null,"start":89794669,"end":89954777,"strand":-1,"description":"EF-hand calcium binding domain 11 [Source:HGNC Symbol;Acc:HGNC:20357]"}, {"versioned_ensembl_gene_id":"ENSG00000124205.15","gene_symbol":"EDN3","gene_name":"endothelin 3 [Source:HGNC Symbol;Acc:HGNC:3178]","synonyms":"ET3","biotype":"protein_coding","ncbi_id":"1908","summary":"The protein encoded by this gene is a member of the endothelin family. Endothelins are endothelium-derived vasoactive peptides involved in a variety of biological functions. The active form of this protein is a 21 amino acid peptide processed from the precursor protein. The active peptide is a ligand for endothelin receptor type B (EDNRB). The interaction of this endothelin with EDNRB is essential for development of neural crest-derived cell lineages, such as melanocytes and enteric neurons. Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":59300427,"end":59325992,"strand":1,"description":"endothelin 3 [Source:HGNC Symbol;Acc:HGNC:3178]"}, {"versioned_ensembl_gene_id":"ENSG00000277801.1","gene_symbol":"AL138478.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89156743,"end":89157574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133265.10","gene_symbol":"HSPBP1","gene_name":"HSPA (Hsp70) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24989]","synonyms":"FES1,HspBP1","biotype":"protein_coding","ncbi_id":"23640","summary":null,"start":55262231,"end":55280381,"strand":-1,"description":"HSPA (Hsp70) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24989]"}, {"versioned_ensembl_gene_id":"ENSG00000256660.5","gene_symbol":"CLEC12B","gene_name":"C-type lectin domain family 12 member B [Source:HGNC Symbol;Acc:HGNC:31966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387837","summary":null,"start":10010627,"end":10018619,"strand":1,"description":"C-type lectin domain family 12 member B [Source:HGNC Symbol;Acc:HGNC:31966]"}, {"versioned_ensembl_gene_id":"ENSG00000259053.1","gene_symbol":"AL137230.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":89412312,"end":89954659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259151.2","gene_symbol":"CAP2P1","gene_name":"cyclase associated actin cytoskeleton regulatory protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20142]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"353163","summary":null,"start":89290205,"end":89291594,"strand":-1,"description":"cyclase associated actin cytoskeleton regulatory protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20142]"}, {"versioned_ensembl_gene_id":"ENSG00000255434.1","gene_symbol":"AP001922.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75596144,"end":75597270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271494.1","gene_symbol":"AC034205.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151380341,"end":151382381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258792.4","gene_symbol":"AL137230.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89628921,"end":89642671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246090.6","gene_symbol":"AP002026.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99088857,"end":99301356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249065.2","gene_symbol":"PCNAP1","gene_name":"proliferating cell nuclear antigen pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8732]","synonyms":"p1PCNA","biotype":"transcribed_processed_pseudogene","ncbi_id":"359806","summary":null,"start":99160514,"end":99161645,"strand":-1,"description":"proliferating cell nuclear antigen pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8732]"}, {"versioned_ensembl_gene_id":"ENSG00000144747.15","gene_symbol":"TMF1","gene_name":"TATA element modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:11870]","synonyms":"TMF,ARA160","biotype":"protein_coding","ncbi_id":"7110","summary":null,"start":69019827,"end":69052303,"strand":-1,"description":"TATA element modulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:11870]"}, {"versioned_ensembl_gene_id":"ENSG00000213777.5","gene_symbol":"AC011487.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53503392,"end":53512687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274892.1","gene_symbol":"AC011487.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53512092,"end":53512616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144339.11","gene_symbol":"TMEFF2","gene_name":"transmembrane protein with EGF like and two follistatin like domains 2 [Source:HGNC Symbol;Acc:HGNC:11867]","synonyms":"TR,TPEF,TENB2,HPP1,CT120.2","biotype":"protein_coding","ncbi_id":"23671","summary":"This gene encodes a member of the tomoregulin family of transmembrane proteins. This protein has been shown to function as both an oncogene and a tumor suppressor depending on the cellular context and may regulate prostate cancer cell invasion. Multiple soluble forms of this protein have been identified that arise from both an alternative splice variant and ectodomain shedding. Additionally, this gene has been found to be hypermethylated in multiple cancer types. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":191949043,"end":192195709,"strand":-1,"description":"transmembrane protein with EGF like and two follistatin like domains 2 [Source:HGNC Symbol;Acc:HGNC:11867]"}, {"versioned_ensembl_gene_id":"ENSG00000148156.7","gene_symbol":"ACTL7B","gene_name":"actin like 7B [Source:HGNC Symbol;Acc:HGNC:162]","synonyms":"Tact1","biotype":"protein_coding","ncbi_id":"10880","summary":"The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":108854589,"end":108856967,"strand":-1,"description":"actin like 7B [Source:HGNC Symbol;Acc:HGNC:162]"}, {"versioned_ensembl_gene_id":"ENSG00000259216.2","gene_symbol":"AC084757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48725338,"end":48725827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259700.3","gene_symbol":"AC012379.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48810701,"end":48811909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204007.6","gene_symbol":"GLT6D1","gene_name":"glycosyltransferase 6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23671]","synonyms":"GLTDC1","biotype":"protein_coding","ncbi_id":"360203","summary":"The GT6 glycosyltransferases gene family, which includes the ABO blood group (ABO; MIM 110300) and GLT6D1, shows a complex evolution pattern, with multiple events of gain and loss in different mammal species. In humans, the ABO gene is considered the sole functional member, although the O allele is null and is fixed in certain populations (summary by Casals et al. (2009) [PubMed 19218399]).[supplied by OMIM, Jan 2011]","start":135623656,"end":135639540,"strand":-1,"description":"glycosyltransferase 6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23671]"}, {"versioned_ensembl_gene_id":"ENSG00000168497.4","gene_symbol":"CAVIN2","gene_name":"caveolae associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10690]","synonyms":"SDR,SDPR,PS-p68,cavin-2","biotype":"protein_coding","ncbi_id":"8436","summary":"This gene encodes a calcium-independent phospholipid-binding protein whose expression increases in serum-starved cells. This protein is a substrate for protein kinase C (PKC) phosphorylation and recruits polymerase I and transcript release factor (PTRF) to caveolae. Removal of this protein causes caveolae loss and its over-expression results in caveolae deformation and membrane tubulation.[provided by RefSeq, Sep 2009]","start":191834302,"end":191847255,"strand":-1,"description":"caveolae associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10690]"}, {"versioned_ensembl_gene_id":"ENSG00000231678.2","gene_symbol":"AL358779.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108701370,"end":108703092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169253.3","gene_symbol":"AL669983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108626833,"end":108627150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233655.1","gene_symbol":"IGHD4-4","gene_name":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]","synonyms":"IGHD44,DA4","biotype":"IG_D_gene","ncbi_id":"28496","summary":null,"start":105913222,"end":105913237,"strand":-1,"description":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]"}, {"versioned_ensembl_gene_id":"ENSG00000236543.2","gene_symbol":"AL354761.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":135604345,"end":135618952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228131.1","gene_symbol":"IGHD6-6","gene_name":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]","synonyms":"IGHD66,D(N4)","biotype":"IG_D_gene","ncbi_id":"28488","summary":null,"start":105910410,"end":105910427,"strand":-1,"description":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]"}, {"versioned_ensembl_gene_id":"ENSG00000233766.7","gene_symbol":"AC098617.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":191846539,"end":192044525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132429.9","gene_symbol":"POPDC3","gene_name":"popeye domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17649]","synonyms":"MGC22671,bA355M14.1,POP3","biotype":"protein_coding","ncbi_id":"64208","summary":"This gene encodes a member of the POP family of proteins containing three putative transmembrane domains. This gene is expressed in cardiac and skeletal muscle and may play an important role in these tissues during development. Alternatively spliced transcript variants have been found. [provided by RefSeq, Nov 2008]","start":105158280,"end":105179995,"strand":-1,"description":"popeye domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17649]"}, {"versioned_ensembl_gene_id":"ENSG00000277632.1","gene_symbol":"CCL3","gene_name":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]","synonyms":"SCYA3,MIP-1-alpha,LD78ALPHA,G0S19-1","biotype":"protein_coding","ncbi_id":"6348","summary":"This locus represents a small inducible cytokine. The encoded protein, also known as macrophage inflammatory protein 1 alpha, plays a role in inflammatory responses through binding to the receptors CCR1, CCR4 and CCR5. Polymorphisms at this locus may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1.[provided by RefSeq, Sep 2010]","start":36088256,"end":36090169,"strand":-1,"description":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]"}, {"versioned_ensembl_gene_id":"ENSG00000132470.13","gene_symbol":"ITGB4","gene_name":"integrin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6158]","synonyms":"CD104","biotype":"protein_coding","ncbi_id":"3691","summary":"Integrins are heterodimers comprised of alpha and beta subunits, that are noncovalently associated transmembrane glycoprotein receptors. Different combinations of alpha and beta polypeptides form complexes that vary in their ligand-binding specificities. Integrins mediate cell-matrix or cell-cell adhesion, and transduced signals that regulate gene expression and cell growth. This gene encodes the integrin beta 4 subunit, a receptor for the laminins. This subunit tends to associate with alpha 6 subunit and is likely to play a pivotal role in the biology of invasive carcinoma. Mutations in this gene are associated with epidermolysis bullosa with pyloric atresia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75721328,"end":75757818,"strand":1,"description":"integrin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6158]"}, {"versioned_ensembl_gene_id":"ENSG00000166763.7","gene_symbol":"STRCP1","gene_name":"stereocilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33915]","synonyms":"STRCP","biotype":"unprocessed_pseudogene","ncbi_id":"554225","summary":null,"start":43699488,"end":43718184,"strand":-1,"description":"stereocilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33915]"}, {"versioned_ensembl_gene_id":"ENSG00000237339.5","gene_symbol":"LINC01502","gene_name":"long intergenic non-protein coding RNA 1502 [Source:HGNC Symbol;Acc:HGNC:51183]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100130954","summary":null,"start":135574935,"end":135587112,"strand":1,"description":"long intergenic non-protein coding RNA 1502 [Source:HGNC Symbol;Acc:HGNC:51183]"}, {"versioned_ensembl_gene_id":"ENSG00000229887.4","gene_symbol":"HNRNPA1P6","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5032]","synonyms":"HNRPA1L,HNRNPA1L1,HNRNPA1L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729423","summary":null,"start":58047889,"end":58049335,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5032]"}, {"versioned_ensembl_gene_id":"ENSG00000277089.4","gene_symbol":"AC243829.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36072866,"end":36090134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261118.1","gene_symbol":"AC092123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89492017,"end":89504460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225231.1","gene_symbol":"LINC02470","gene_name":"long intergenic non-protein coding RNA 2470 [Source:HGNC Symbol;Acc:HGNC:53409]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506159","summary":null,"start":9936579,"end":9943495,"strand":-1,"description":"long intergenic non-protein coding RNA 2470 [Source:HGNC Symbol;Acc:HGNC:53409]"}, {"versioned_ensembl_gene_id":"ENSG00000261517.1","gene_symbol":"LINC00558","gene_name":"long intergenic non-protein coding RNA 558 [Source:HGNC Symbol;Acc:HGNC:43702]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861552","summary":null,"start":53815419,"end":53876119,"strand":1,"description":"long intergenic non-protein coding RNA 558 [Source:HGNC Symbol;Acc:HGNC:43702]"}, {"versioned_ensembl_gene_id":"ENSG00000198346.10","gene_symbol":"ZNF813","gene_name":"zinc finger protein 813 [Source:HGNC Symbol;Acc:HGNC:33257]","synonyms":"FLJ16542","biotype":"protein_coding","ncbi_id":"126017","summary":null,"start":53467735,"end":53496255,"strand":1,"description":"zinc finger protein 813 [Source:HGNC Symbol;Acc:HGNC:33257]"}, {"versioned_ensembl_gene_id":"ENSG00000255357.1","gene_symbol":"AC055878.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22492112,"end":22502846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230936.1","gene_symbol":"AC073347.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55342316,"end":55344958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242076.2","gene_symbol":"IGKV1-33","gene_name":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]","synonyms":"IGKV133,O18","biotype":"IG_V_gene","ncbi_id":"28933","summary":null,"start":89266494,"end":89268506,"strand":-1,"description":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]"}, {"versioned_ensembl_gene_id":"ENSG00000241434.1","gene_symbol":"AC022137.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53495887,"end":53496037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255323.5","gene_symbol":"LINC01495","gene_name":"long intergenic non-protein coding RNA 1495 [Source:HGNC Symbol;Acc:HGNC:51161]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723378","summary":null,"start":22445688,"end":22492019,"strand":-1,"description":"long intergenic non-protein coding RNA 1495 [Source:HGNC Symbol;Acc:HGNC:51161]"}, {"versioned_ensembl_gene_id":"ENSG00000198099.8","gene_symbol":"ADH4","gene_name":"alcohol dehydrogenase 4 (class II), pi polypeptide [Source:HGNC Symbol;Acc:HGNC:252]","synonyms":"ADH-2","biotype":"protein_coding","ncbi_id":"127","summary":"This gene encodes class II alcohol dehydrogenase 4 pi subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class II alcohol dehydrogenase is a homodimer composed of 2 pi subunits. It exhibits a high activity for oxidation of long-chain aliphatic alcohols and aromatic alcohols and is less sensitive to pyrazole. This gene is localized to chromosome 4 in the cluster of alcohol dehydrogenase genes. [provided by RefSeq, Jul 2008]","start":99123657,"end":99157792,"strand":-1,"description":"alcohol dehydrogenase 4 (class II), pi polypeptide [Source:HGNC Symbol;Acc:HGNC:252]"}, {"versioned_ensembl_gene_id":"ENSG00000252128.1","gene_symbol":"SNORD27","gene_name":"Small nucleolar RNA SNORD27 [Source:RFAM;Acc:RF00086]","synonyms":"U27,RNU27","biotype":"snoRNA","ncbi_id":"9301","summary":null,"start":21139886,"end":21139957,"strand":-1,"description":"Small nucleolar RNA SNORD27 [Source:RFAM;Acc:RF00086]"}, {"versioned_ensembl_gene_id":"ENSG00000227234.1","gene_symbol":"SPANXB1","gene_name":"SPANX family member B1 [Source:HGNC Symbol;Acc:HGNC:14329]","synonyms":"SPANXF2,SPANXF1,SPANXB2,CT11.2","biotype":"protein_coding","ncbi_id":"728695","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular family member contains an additional 18 nucleotides in its coding region compared to the other family members in the same gene cluster. This family member is also subject to gene copy number variation. Although the protein encoded by this gene contains consensus nuclear localization signals, the major site for subcellular localization of expressed protein is in the cytoplasmic droplets of ejaculated spermatozoa. This protein provides a biochemical marker for studying the unique structures in spermatazoa, while attempting to further define its role in spermatogenesis. [provided by RefSeq, Apr 2014]","start":141002591,"end":141003706,"strand":1,"description":"SPANX family member B1 [Source:HGNC Symbol;Acc:HGNC:14329]"}, {"versioned_ensembl_gene_id":"ENSG00000134955.11","gene_symbol":"SLC37A2","gene_name":"solute carrier family 37 member 2 [Source:HGNC Symbol;Acc:HGNC:20644]","synonyms":"FLJ00171","biotype":"protein_coding","ncbi_id":"219855","summary":null,"start":125063067,"end":125090312,"strand":1,"description":"solute carrier family 37 member 2 [Source:HGNC Symbol;Acc:HGNC:20644]"}, {"versioned_ensembl_gene_id":"ENSG00000122406.12","gene_symbol":"RPL5","gene_name":"ribosomal protein L5 [Source:HGNC Symbol;Acc:HGNC:10360]","synonyms":"PPP1R135,L5","biotype":"protein_coding","ncbi_id":"6125","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18P family of ribosomal proteins and component of the 60S subunit. The encoded protein binds 5S rRNA to form a stable complex called the 5S ribonucleoprotein particle (RNP), which is necessary for the transport of nonribosome-associated cytoplasmic 5S rRNA to the nucleolus for assembly into ribosomes. The encoded protein may also function to inhibit tumorigenesis through the activation of downstream tumor suppressors and the downregulation of oncoprotein expression. Mutations in this gene have been identified in patients with Diamond-Blackfan Anemia (DBA). This gene is co-transcribed with the small nucleolar RNA gene U21, which is located in its fifth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. [provided by RefSeq, Mar 2017]","start":92832025,"end":92841924,"strand":1,"description":"ribosomal protein L5 [Source:HGNC Symbol;Acc:HGNC:10360]"}, {"versioned_ensembl_gene_id":"ENSG00000273919.1","gene_symbol":"AL450423.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53345211,"end":53410880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229269.1","gene_symbol":"AL451048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140931738,"end":140997448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213557.4","gene_symbol":"AC068050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108040213,"end":108040592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163394.5","gene_symbol":"CCKAR","gene_name":"cholecystokinin A receptor [Source:HGNC Symbol;Acc:HGNC:1570]","synonyms":null,"biotype":"protein_coding","ncbi_id":"886","summary":"This gene encodes a G-protein coupled receptor that binds non-sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine. [provided by RefSeq, Jul 2008]","start":26481400,"end":26490462,"strand":-1,"description":"cholecystokinin A receptor [Source:HGNC Symbol;Acc:HGNC:1570]"}, {"versioned_ensembl_gene_id":"ENSG00000231616.8","gene_symbol":"AL354733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83831586,"end":83868532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231293.1","gene_symbol":"RPL36AP6","gene_name":"ribosomal protein L36a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23365]","synonyms":"bA380I20.1","biotype":"processed_pseudogene","ncbi_id":"641556","summary":null,"start":107834509,"end":107834829,"strand":-1,"description":"ribosomal protein L36a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23365]"}, {"versioned_ensembl_gene_id":"ENSG00000177380.13","gene_symbol":"PPFIA3","gene_name":"PTPRF interacting protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:9247]","synonyms":"MGC126569,MGC126567,LPNA3,KIAA0654","biotype":"protein_coding","ncbi_id":"8541","summary":"The protein encoded by this gene is a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. Liprins interact with members of LAR family of transmembrane protein tyrosine phosphatases, which are known to be important for axon guidance and mammary gland development. Liprin family protein has been shown to localize phosphatase LAR to cell focal adhesions and may be involved in the molecular organization of presynaptic active zones. [provided by RefSeq, Jul 2008]","start":49119389,"end":49151026,"strand":1,"description":"PTPRF interacting protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:9247]"}, {"versioned_ensembl_gene_id":"ENSG00000225510.2","gene_symbol":"PCDH8P1","gene_name":"protocadherin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39937]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100133285","summary":null,"start":53199981,"end":53202753,"strand":1,"description":"protocadherin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39937]"}, {"versioned_ensembl_gene_id":"ENSG00000243238.1","gene_symbol":"IGKV2-30","gene_name":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28919","summary":null,"start":89244781,"end":89245596,"strand":-1,"description":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]"}, {"versioned_ensembl_gene_id":"ENSG00000248725.3","gene_symbol":"AC097488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85246157,"end":85246912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226499.1","gene_symbol":"AL136380.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44843921,"end":44844082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162600.11","gene_symbol":"OMA1","gene_name":"OMA1 zinc metallopeptidase [Source:HGNC Symbol;Acc:HGNC:29661]","synonyms":"ZMPOMA1,YKR087C,MPRP-1,FLJ33782","biotype":"protein_coding","ncbi_id":"115209","summary":null,"start":58415384,"end":58546802,"strand":-1,"description":"OMA1 zinc metallopeptidase [Source:HGNC Symbol;Acc:HGNC:29661]"}, {"versioned_ensembl_gene_id":"ENSG00000130427.2","gene_symbol":"EPO","gene_name":"erythropoietin [Source:HGNC Symbol;Acc:HGNC:3415]","synonyms":"EP","biotype":"protein_coding","ncbi_id":"2056","summary":"This gene encodes a secreted, glycosylated cytokine composed of four alpha helical bundles. The encoded protein is mainly synthesized in the kidney, secreted into the blood plasma, and binds to the erythropoietin receptor to promote red blood cell production, or erythropoiesis, in the bone marrow. Expression of this gene is upregulated under hypoxic conditions, in turn leading to increased erythropoiesis and enhanced oxygen-carrying capacity of the blood. Expression of this gene has also been observed in brain and in the eye, and elevated expression levels have been observed in diabetic retinopathy and ocular hypertension. Recombinant forms of the encoded protein exhibit neuroprotective activity against a variety of potential brain injuries, as well as antiapoptotic functions in several tissue types, and have been used in the treatment of anemia and to enhance the efficacy of cancer therapies. [provided by RefSeq, Aug 2017]","start":100720800,"end":100723700,"strand":1,"description":"erythropoietin [Source:HGNC Symbol;Acc:HGNC:3415]"}, {"versioned_ensembl_gene_id":"ENSG00000172273.12","gene_symbol":"HINFP","gene_name":"histone H4 transcription factor [Source:HGNC Symbol;Acc:HGNC:17850]","synonyms":"MIZF,HiNF-P,DKFZP434F162,ZNF743","biotype":"protein_coding","ncbi_id":"25988","summary":"This gene encodes a transcription factor that interacts with methyl-CpG-binding protein-2 (MBD2), a component of the MeCP1 histone deacetylase (HDAC) complex, and plays a role in DNA methylation and transcription repression. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Aug 2011]","start":119121587,"end":119136044,"strand":1,"description":"histone H4 transcription factor [Source:HGNC Symbol;Acc:HGNC:17850]"}, {"versioned_ensembl_gene_id":"ENSG00000270202.1","gene_symbol":"AP003973.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111107060,"end":111107750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188599.17","gene_symbol":"NPIPP1","gene_name":"nuclear pore complex interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35407]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100874381","summary":null,"start":15104312,"end":15123498,"strand":-1,"description":"nuclear pore complex interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35407]"}, {"versioned_ensembl_gene_id":"ENSG00000259670.1","gene_symbol":"AC012379.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48783190,"end":48784121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281508.1","gene_symbol":"CDR1","gene_name":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]","synonyms":"CDR,CDR62A,CDR34,CDR,CDR62A,CDR34","biotype":"antisense_RNA","ncbi_id":"1038","summary":"Autoantibodies directed against the protein encoded by this intronless gene have been found in some patients with paraneoplastic cerebellar degeneration. The encoded protein contains several hexapeptide repeats. [provided by RefSeq, Jan 2010]","start":140783176,"end":140784660,"strand":1,"description":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]"}, {"versioned_ensembl_gene_id":"ENSG00000184258.6","gene_symbol":"CDR1","gene_name":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]","synonyms":"CDR,CDR62A,CDR34,CDR,CDR62A,CDR34","biotype":"protein_coding","ncbi_id":"1038","summary":"Autoantibodies directed against the protein encoded by this intronless gene have been found in some patients with paraneoplastic cerebellar degeneration. The encoded protein contains several hexapeptide repeats. [provided by RefSeq, Jan 2010]","start":140782405,"end":140784871,"strand":-1,"description":"cerebellar degeneration related protein 1 [Source:HGNC Symbol;Acc:HGNC:1798]"}, {"versioned_ensembl_gene_id":"ENSG00000279325.1","gene_symbol":"AL136359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53193667,"end":53198540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255149.1","gene_symbol":"AP002963.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110876994,"end":110877177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237092.1","gene_symbol":"LINC01065","gene_name":"long intergenic non-protein coding RNA 1065 [Source:HGNC Symbol;Acc:HGNC:49103]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723875","summary":null,"start":53146539,"end":53151808,"strand":-1,"description":"long intergenic non-protein coding RNA 1065 [Source:HGNC Symbol;Acc:HGNC:49103]"}, {"versioned_ensembl_gene_id":"ENSG00000233497.4","gene_symbol":"HNRNPA1P60","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48790]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"120364","summary":null,"start":110788026,"end":110788976,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48790]"}, {"versioned_ensembl_gene_id":"ENSG00000254098.1","gene_symbol":"IGKV2-26","gene_name":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28922","summary":null,"start":89196096,"end":89196829,"strand":-1,"description":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]"}, {"versioned_ensembl_gene_id":"ENSG00000253202.1","gene_symbol":"IGKV3-25","gene_name":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28911","summary":null,"start":89192500,"end":89192752,"strand":-1,"description":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]"}, {"versioned_ensembl_gene_id":"ENSG00000172336.4","gene_symbol":"POP7","gene_name":"POP7 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:19949]","synonyms":"RPP20,RPP2","biotype":"protein_coding","ncbi_id":"10248","summary":null,"start":100706053,"end":100707495,"strand":1,"description":"POP7 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:19949]"}, {"versioned_ensembl_gene_id":"ENSG00000189042.13","gene_symbol":"ZNF567","gene_name":"zinc finger protein 567 [Source:HGNC Symbol;Acc:HGNC:28696]","synonyms":"MGC45586","biotype":"protein_coding","ncbi_id":"163081","summary":null,"start":36687612,"end":36727701,"strand":1,"description":"zinc finger protein 567 [Source:HGNC Symbol;Acc:HGNC:28696]"}, {"versioned_ensembl_gene_id":"ENSG00000206517.12","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425381,"end":29456943,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000241294.1","gene_symbol":"IGKV2-24","gene_name":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28923","summary":null,"start":89176328,"end":89177160,"strand":-1,"description":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]"}, {"versioned_ensembl_gene_id":"ENSG00000230668.1","gene_symbol":"AL844175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140681106,"end":140687705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197912.14","gene_symbol":"SPG7","gene_name":"SPG7, paraplegin matrix AAA peptidase subunit [Source:HGNC Symbol;Acc:HGNC:11237]","synonyms":"SPG5C,CMAR,CAR","biotype":"protein_coding","ncbi_id":"6687","summary":"This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]","start":89490917,"end":89557768,"strand":1,"description":"SPG7, paraplegin matrix AAA peptidase subunit [Source:HGNC Symbol;Acc:HGNC:11237]"}, {"versioned_ensembl_gene_id":"ENSG00000274627.1","gene_symbol":"AC092123.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89516797,"end":89522217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196083.9","gene_symbol":"IL1RAP","gene_name":"interleukin 1 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5995]","synonyms":"IL1R3,IL-1RAcP,C3orf13","biotype":"protein_coding","ncbi_id":"3556","summary":"This gene encodes a component of the interleukin 1 receptor complex, which initiates signalling events that result in the activation of interleukin 1-responsive genes. Alternative splicing of this gene results in membrane-bound and soluble isoforms differing in their C-terminus. The ratio of soluble to membrane-bound forms increases during acute-phase induction or stress. [provided by RefSeq, Jul 2018]","start":190514051,"end":190659750,"strand":1,"description":"interleukin 1 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:5995]"}, {"versioned_ensembl_gene_id":"ENSG00000273370.1","gene_symbol":"AC108747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":190659216,"end":190659750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186335.8","gene_symbol":"SLC36A2","gene_name":"solute carrier family 36 member 2 [Source:HGNC Symbol;Acc:HGNC:18762]","synonyms":"tramdorin,TRAMD1,PAT2","biotype":"protein_coding","ncbi_id":"153201","summary":"This gene encodes a pH-dependent proton-coupled amino acid transporter that belongs to the amino acid auxin permease 1 protein family. The encoded protein primarily transports small amino acids such as glycine, alanine and proline. Mutations in this gene are associated with iminoglycinuria and hyperglycinuria. [provided by RefSeq, Sep 2010]","start":151314978,"end":151347590,"strand":-1,"description":"solute carrier family 36 member 2 [Source:HGNC Symbol;Acc:HGNC:18762]"}, {"versioned_ensembl_gene_id":"ENSG00000114854.7","gene_symbol":"TNNC1","gene_name":"troponin C1, slow skeletal and cardiac type [Source:HGNC Symbol;Acc:HGNC:11943]","synonyms":"TNNC","biotype":"protein_coding","ncbi_id":"7134","summary":"Troponin is a central regulatory protein of striated muscle contraction, and together with tropomyosin, is located on the actin filament. Troponin consists of 3 subunits: TnI, which is the inhibitor of actomyosin ATPase; TnT, which contains the binding site for tropomyosin; and TnC, the protein encoded by this gene. The binding of calcium to TnC abolishes the inhibitory action of TnI, thus allowing the interaction of actin with myosin, the hydrolysis of ATP, and the generation of tension. Mutations in this gene are associated with cardiomyopathy dilated type 1Z. [provided by RefSeq, Oct 2008]","start":52451102,"end":52454070,"strand":-1,"description":"troponin C1, slow skeletal and cardiac type [Source:HGNC Symbol;Acc:HGNC:11943]"}, {"versioned_ensembl_gene_id":"ENSG00000228615.1","gene_symbol":"AC093166.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111742586,"end":111744662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227842.1","gene_symbol":"AC093166.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111717508,"end":111717837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211920.1","gene_symbol":"IGHD6-13","gene_name":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]","synonyms":"IGHD613,DN1","biotype":"IG_D_gene","ncbi_id":"28487","summary":null,"start":105901142,"end":105901162,"strand":-1,"description":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]"}, {"versioned_ensembl_gene_id":"ENSG00000227108.1","gene_symbol":"IGHD1-14","gene_name":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]","synonyms":"IGHD114,DM2","biotype":"IG_D_gene","ncbi_id":"28508","summary":null,"start":105900638,"end":105900654,"strand":-1,"description":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]"}, {"versioned_ensembl_gene_id":"ENSG00000278234.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":150241777,"end":150241860,"strand":1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000241015.2","gene_symbol":"TPM3P9","gene_name":"tropomyosin 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44142]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"147804","summary":null,"start":53431984,"end":53444670,"strand":1,"description":"tropomyosin 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44142]"}, {"versioned_ensembl_gene_id":"ENSG00000182154.7","gene_symbol":"MRPL41","gene_name":"mitochondrial ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:14492]","synonyms":"RPML27,PIG3,MRPL27,MRP-L27,BMRP","biotype":"protein_coding","ncbi_id":"64975","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the YmL27 ribosomal protein family. [provided by RefSeq, Jul 2008]","start":137551199,"end":137552555,"strand":1,"description":"mitochondrial ribosomal protein L41 [Source:HGNC Symbol;Acc:HGNC:14492]"}, {"versioned_ensembl_gene_id":"ENSG00000172460.16","gene_symbol":"PRSS30P","gene_name":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]","synonyms":"TMPRSS8P,TMPRSS8,MGC5228,Disp","biotype":"transcribed_unitary_pseudogene","ncbi_id":"124221","summary":null,"start":2839568,"end":2842744,"strand":-1,"description":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]"}, {"versioned_ensembl_gene_id":"ENSG00000211915.1","gene_symbol":"IGHD5-18","gene_name":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]","synonyms":"IGHD518","biotype":"IG_D_gene","ncbi_id":"28490","summary":null,"start":105893542,"end":105893561,"strand":-1,"description":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]"}, {"versioned_ensembl_gene_id":"ENSG00000237020.1","gene_symbol":"IGHD1-20","gene_name":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]","synonyms":"IGHD120","biotype":"IG_D_gene","ncbi_id":"28507","summary":null,"start":105891191,"end":105891207,"strand":-1,"description":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]"}, {"versioned_ensembl_gene_id":"ENSG00000211914.1","gene_symbol":"IGHD6-19","gene_name":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]","synonyms":"IGHD619","biotype":"IG_D_gene","ncbi_id":"28486","summary":null,"start":105891699,"end":105891719,"strand":-1,"description":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]"}, {"versioned_ensembl_gene_id":"ENSG00000227800.1","gene_symbol":"IGHD4-17","gene_name":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]","synonyms":"IGHD417","biotype":"IG_D_gene","ncbi_id":"28494","summary":null,"start":105894508,"end":105894523,"strand":-1,"description":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]"}, {"versioned_ensembl_gene_id":"ENSG00000107833.10","gene_symbol":"NPM3","gene_name":"nucleophosmin/nucleoplasmin 3 [Source:HGNC Symbol;Acc:HGNC:7931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10360","summary":"The protein encoded by this gene is related to the nuclear chaperone phosphoproteins, nucleoplasmin and nucleophosmin. This protein is strongly expressed in diverse cell types where it localizes primarily to the nucleus. Based on its similarity to nucleoplasmin and nucleophosmin, this protein likely functions as a molecular chaperone in the cell nucleus. [provided by RefSeq, Oct 2008]","start":101781325,"end":101783413,"strand":-1,"description":"nucleophosmin/nucleoplasmin 3 [Source:HGNC Symbol;Acc:HGNC:7931]"}, {"versioned_ensembl_gene_id":"ENSG00000244620.1","gene_symbol":"AC246787.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105890084,"end":105896577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279953.1","gene_symbol":"AC117503.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123649068,"end":123650485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224818.1","gene_symbol":"AC096677.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":201464383,"end":201465146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260558.1","gene_symbol":"AC018557.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66738263,"end":66739326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246777.1","gene_symbol":"AC044802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66751752,"end":66754740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162078.11","gene_symbol":"ZG16B","gene_name":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]","synonyms":"PRO1567,JCLN2,HRPE773","biotype":"protein_coding","ncbi_id":"124220","summary":null,"start":2830169,"end":2839585,"strand":1,"description":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]"}, {"versioned_ensembl_gene_id":"ENSG00000260465.1","gene_symbol":"AC018557.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66720897,"end":66731785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168955.3","gene_symbol":"TM4SF20","gene_name":"transmembrane 4 L six family member 20 [Source:HGNC Symbol;Acc:HGNC:26230]","synonyms":"TCCE518,FLJ22800","biotype":"protein_coding","ncbi_id":"79853","summary":"The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016]","start":227362156,"end":227381995,"strand":-1,"description":"transmembrane 4 L six family member 20 [Source:HGNC Symbol;Acc:HGNC:26230]"}, {"versioned_ensembl_gene_id":"ENSG00000243492.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLA-92,HLAL,HLA92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30249483,"end":30256765,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000112167.9","gene_symbol":"SAYSD1","gene_name":"SAYSVFN motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21025]","synonyms":"FLJ11101,C6orf64","biotype":"protein_coding","ncbi_id":"55776","summary":null,"start":39104064,"end":39115189,"strand":-1,"description":"SAYSVFN motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21025]"}, {"versioned_ensembl_gene_id":"ENSG00000203809.6","gene_symbol":"LIN28B-AS1","gene_name":"LIN28B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21553]","synonyms":"LINC00577,dJ439I14.1,C6orf220","biotype":"lincRNA","ncbi_id":"100113403","summary":null,"start":104864464,"end":104941447,"strand":-1,"description":"LIN28B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21553]"}, {"versioned_ensembl_gene_id":"ENSG00000111364.15","gene_symbol":"DDX55","gene_name":"DEAD-box helicase 55 [Source:HGNC Symbol;Acc:HGNC:20085]","synonyms":"KIAA1595","biotype":"protein_coding","ncbi_id":"57696","summary":"This gene encodes a member of protein family containing a characteristic Asp-Glu-Ala-Asp (DEAD) motif. These proteins are putative RNA helicases, and may be involved in a range of nuclear processes including translational initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Multiple alternatively spliced transcript variants have been found for this gene. Pseudogenes have been identified on chromosomes 1 and 12. [provided by RefSeq, Feb 2016]","start":123602077,"end":123620941,"strand":1,"description":"DEAD-box helicase 55 [Source:HGNC Symbol;Acc:HGNC:20085]"}, {"versioned_ensembl_gene_id":"ENSG00000276570.1","gene_symbol":"AC010327.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55227219,"end":55230279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241863.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30319108,"end":30336684,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000211911.1","gene_symbol":"IGHD3-22","gene_name":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]","synonyms":"IGHD322","biotype":"IG_D_gene","ncbi_id":"28497","summary":null,"start":105886031,"end":105886061,"strand":-1,"description":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]"}, {"versioned_ensembl_gene_id":"ENSG00000148513.17","gene_symbol":"ANKRD30A","gene_name":"ankyrin repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:17234]","synonyms":"NY-BR-1","biotype":"protein_coding","ncbi_id":"91074","summary":"This gene encodes a DNA-binding transcription factor that is uniquely expressed in mammary epithelium and the testis. Altered expression levels have been associated with breast cancer progression. [provided by RefSeq, Nov 2016]","start":37125788,"end":37384111,"strand":1,"description":"ankyrin repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:17234]"}, {"versioned_ensembl_gene_id":"ENSG00000276071.1","gene_symbol":"AC074138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36668102,"end":36669404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186334.9","gene_symbol":"SLC36A3","gene_name":"solute carrier family 36 member 3 [Source:HGNC Symbol;Acc:HGNC:19659]","synonyms":"tramdorin2,TRAMD2,PAT3","biotype":"protein_coding","ncbi_id":"285641","summary":null,"start":151276762,"end":151303766,"strand":-1,"description":"solute carrier family 36 member 3 [Source:HGNC Symbol;Acc:HGNC:19659]"}, {"versioned_ensembl_gene_id":"ENSG00000259469.1","gene_symbol":"AC084757.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48729080,"end":48729844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228894.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ31598,FLJ25550,Em:AB014087.1","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30280607,"end":30316946,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000225825.1","gene_symbol":"IGHD6-25","gene_name":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]","synonyms":"IGHD625","biotype":"IG_D_gene","ncbi_id":"28485","summary":null,"start":105881539,"end":105881556,"strand":-1,"description":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]"}, {"versioned_ensembl_gene_id":"ENSG00000134595.8","gene_symbol":"SOX3","gene_name":"SRY-box 3 [Source:HGNC Symbol;Acc:HGNC:11199]","synonyms":"PHP","biotype":"protein_coding","ncbi_id":"6658","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked cognitive disability with growth hormone deficiency. [provided by RefSeq, Jul 2008]","start":140502985,"end":140505116,"strand":-1,"description":"SRY-box 3 [Source:HGNC Symbol;Acc:HGNC:11199]"}, {"versioned_ensembl_gene_id":"ENSG00000227335.1","gene_symbol":"IGHJ1P","gene_name":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]","synonyms":"Jpsi1","biotype":"IG_J_pseudogene","ncbi_id":"28482","summary":null,"start":105865624,"end":105865678,"strand":-1,"description":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]"}, {"versioned_ensembl_gene_id":"ENSG00000236597.1","gene_symbol":"IGHD7-27","gene_name":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]","synonyms":"IGHD727,DHQ52","biotype":"IG_D_gene","ncbi_id":"28484","summary":null,"start":105865551,"end":105865561,"strand":-1,"description":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]"}, {"versioned_ensembl_gene_id":"ENSG00000240041.1","gene_symbol":"IGHJ4","gene_name":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28477","summary":null,"start":105864215,"end":105864260,"strand":-1,"description":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]"}, {"versioned_ensembl_gene_id":"ENSG00000161526.14","gene_symbol":"SAP30BP","gene_name":"SAP30 binding protein [Source:HGNC Symbol;Acc:HGNC:30785]","synonyms":"HTRP,HTRG,HCNGP","biotype":"protein_coding","ncbi_id":"29115","summary":null,"start":75667116,"end":75708062,"strand":1,"description":"SAP30 binding protein [Source:HGNC Symbol;Acc:HGNC:30785]"}, {"versioned_ensembl_gene_id":"ENSG00000101079.20","gene_symbol":"NDRG3","gene_name":"NDRG family member 3 [Source:HGNC Symbol;Acc:HGNC:14462]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57446","summary":null,"start":36651766,"end":36746078,"strand":-1,"description":"NDRG family member 3 [Source:HGNC Symbol;Acc:HGNC:14462]"}, {"versioned_ensembl_gene_id":"ENSG00000229944.3","gene_symbol":"EIF4EP2","gene_name":"eukaryotic translation initiation factor 4E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131693","summary":null,"start":49424269,"end":49424922,"strand":-1,"description":"eukaryotic translation initiation factor 4E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32428]"}, {"versioned_ensembl_gene_id":"ENSG00000186244.7","gene_symbol":"AC091180.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49400429,"end":49400800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262039.1","gene_symbol":"AC091180.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49370740,"end":49476988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249302.2","gene_symbol":"FTH1P24","gene_name":"ferritin heavy chain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37642]","synonyms":"FTHL24","biotype":"processed_pseudogene","ncbi_id":"100462797","summary":null,"start":139546266,"end":139546727,"strand":1,"description":"ferritin heavy chain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37642]"}, {"versioned_ensembl_gene_id":"ENSG00000174175.16","gene_symbol":"SELP","gene_name":"selectin P [Source:HGNC Symbol;Acc:HGNC:10721]","synonyms":"PSEL,PADGEM,GRMP,GMP140,CD62P,CD62","biotype":"protein_coding","ncbi_id":"6403","summary":"This gene encodes a 140 kDa protein that is stored in the alpha-granules of platelets and Weibel-Palade bodies of endothelial cells. This protein redistributes to the plasma membrane during platelet activation and degranulation and mediates the interaction of activated endothelial cells or platelets with leukocytes. The membrane protein is a calcium-dependent receptor that binds to sialylated forms of Lewis blood group carbohydrate antigens on neutrophils and monocytes. Alternative splice variants may occur but are not well documented. [provided by RefSeq, Jul 2008]","start":169588849,"end":169630193,"strand":-1,"description":"selectin P [Source:HGNC Symbol;Acc:HGNC:10721]"}, {"versioned_ensembl_gene_id":"ENSG00000134987.11","gene_symbol":"WDR36","gene_name":"WD repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:30696]","synonyms":"UTP21,TA-WDRP,GLC1G","biotype":"protein_coding","ncbi_id":"134430","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Mutations in this gene have been associated with adult-onset primary open-angle glaucoma (POAG). [provided by RefSeq, Jul 2008]","start":111091716,"end":111130502,"strand":1,"description":"WD repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:30696]"}, {"versioned_ensembl_gene_id":"ENSG00000244703.3","gene_symbol":"CD46P1","gene_name":"CD46 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6959]","synonyms":"MCPL,CD46P","biotype":"unprocessed_pseudogene","ncbi_id":"4182","summary":null,"start":207645234,"end":207657410,"strand":1,"description":"CD46 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6959]"}, {"versioned_ensembl_gene_id":"ENSG00000259161.2","gene_symbol":"AL137779.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101843394,"end":101844122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259088.1","gene_symbol":"AL137779.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101796555,"end":101810321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120725.12","gene_symbol":"SIL1","gene_name":"SIL1 nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:24624]","synonyms":"ULG5,MSS,BAP","biotype":"protein_coding","ncbi_id":"64374","summary":"This gene encodes a resident endoplasmic reticulum (ER), N-linked glycoprotein with an N-terminal ER targeting sequence, 2 putative N-glycosylation sites, and a C-terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco-Sjogren syndrome. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":138946720,"end":139293557,"strand":-1,"description":"SIL1 nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:24624]"}, {"versioned_ensembl_gene_id":"ENSG00000236478.2","gene_symbol":"AC012513.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":216174896,"end":216176032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188393.8","gene_symbol":"CLEC2A","gene_name":"C-type lectin domain family 2 member A [Source:HGNC Symbol;Acc:HGNC:24191]","synonyms":"INPE5792,UNQ5792,PILAR,KACL","biotype":"protein_coding","ncbi_id":"387836","summary":"CLEC2A belongs to the CLEC2 family of activation-induced, natural killer gene complex-encoded C-type lectin-like receptors (Spreu et al., 2007 [PubMed 18046548]).[supplied by OMIM, May 2008]","start":9898673,"end":9932381,"strand":-1,"description":"C-type lectin domain family 2 member A [Source:HGNC Symbol;Acc:HGNC:24191]"}, {"versioned_ensembl_gene_id":"ENSG00000239951.1","gene_symbol":"IGKV3-20","gene_name":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28912","summary":null,"start":89142574,"end":89143160,"strand":-1,"description":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]"}, {"versioned_ensembl_gene_id":"ENSG00000157227.12","gene_symbol":"MMP14","gene_name":"matrix metallopeptidase 14 [Source:HGNC Symbol;Acc:HGNC:7160]","synonyms":"MT1-MMP","biotype":"protein_coding","ncbi_id":"4323","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily; each member of this subfamily contains a potential transmembrane domain suggesting that these proteins are expressed at the cell surface rather than secreted. This protein activates MMP2 protein, and this activity may be involved in tumor invasion. [provided by RefSeq, Jul 2008]","start":22836557,"end":22849027,"strand":1,"description":"matrix metallopeptidase 14 [Source:HGNC Symbol;Acc:HGNC:7160]"}, {"versioned_ensembl_gene_id":"ENSG00000197808.11","gene_symbol":"ZNF461","gene_name":"zinc finger protein 461 [Source:HGNC Symbol;Acc:HGNC:21629]","synonyms":"MGC33911,GIOT-1","biotype":"protein_coding","ncbi_id":"92283","summary":null,"start":36637192,"end":36666853,"strand":-1,"description":"zinc finger protein 461 [Source:HGNC Symbol;Acc:HGNC:21629]"}, {"versioned_ensembl_gene_id":"ENSG00000239912.1","gene_symbol":"RPL39P36","gene_name":"ribosomal protein L39 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271526","summary":null,"start":53413190,"end":53413345,"strand":1,"description":"ribosomal protein L39 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36076]"}, {"versioned_ensembl_gene_id":"ENSG00000224994.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30316275,"end":30333529,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000136861.17","gene_symbol":"CDK5RAP2","gene_name":"CDK5 regulatory subunit associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18672]","synonyms":"CEP215,C48,MCPH3,FLJ10867","biotype":"protein_coding","ncbi_id":"55755","summary":"This gene encodes a regulator of CDK5 (cyclin-dependent kinase 5) activity. The protein encoded by this gene is localized to the centrosome and Golgi complex, interacts with CDK5R1 and pericentrin (PCNT), plays a role in centriole engagement and microtubule nucleation, and has been linked to primary microcephaly and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":120388869,"end":120580170,"strand":-1,"description":"CDK5 regulatory subunit associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18672]"}, {"versioned_ensembl_gene_id":"ENSG00000248428.1","gene_symbol":"AC010395.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110970951,"end":111008899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274736.4","gene_symbol":"CCL23","gene_name":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]","synonyms":"SCYA23,MPIF-1,MIP-3,CKb8,Ckb-8","biotype":"protein_coding","ncbi_id":"6368","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, displays chemotactic activity on resting T lymphocytes and monocytes, lower activity on neutrophils and no activity on activated T lymphocytes. The protein is also a strong suppressor of colony formation by a multipotential hematopoietic progenitor cell line. In addition, the product of this gene is a potent agonist of the chemokine (C-C motif) receptor 1. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":36013056,"end":36017968,"strand":-1,"description":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]"}, {"versioned_ensembl_gene_id":"ENSG00000278690.1","gene_symbol":"AC244100.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36012504,"end":36012891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079246.15","gene_symbol":"XRCC5","gene_name":"X-ray repair cross complementing 5 [Source:HGNC Symbol;Acc:HGNC:12833]","synonyms":"KUB2,Ku86,KU80,KARP-1","biotype":"protein_coding","ncbi_id":"7520","summary":"The protein encoded by this gene is the 80-kilodalton subunit of the Ku heterodimer protein which is also known as ATP-dependant DNA helicase II or DNA repair protein XRCC5. Ku is the DNA-binding component of the DNA-dependent protein kinase, and it functions together with the DNA ligase IV-XRCC4 complex in the repair of DNA double-strand break by non-homologous end joining and the completion of V(D)J recombination events. This gene functionally complements Chinese hamster xrs-6, a mutant defective in DNA double-strand break repair and in ability to undergo V(D)J recombination. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008]","start":216107464,"end":216206303,"strand":1,"description":"X-ray repair cross complementing 5 [Source:HGNC Symbol;Acc:HGNC:12833]"}, {"versioned_ensembl_gene_id":"ENSG00000117425.13","gene_symbol":"PTCH2","gene_name":"patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8643","summary":"This gene encodes a transmembrane receptor of the patched gene family. The encoded protein may function as a tumor suppressor in the hedgehog signaling pathway. Alterations in this gene have been associated with nevoid basal cell carcinoma syndrome, basal cell carcinoma, medulloblastoma, and susceptibility to congenital macrostomia. Alternatively spliced transcript variants have been described.[provided by RefSeq, Oct 2009]","start":44819844,"end":44843063,"strand":-1,"description":"patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]"}, {"versioned_ensembl_gene_id":"ENSG00000170615.14","gene_symbol":"SLC26A5","gene_name":"solute carrier family 26 member 5 [Source:HGNC Symbol;Acc:HGNC:9359]","synonyms":"PRES,DFNB61","biotype":"protein_coding","ncbi_id":"375611","summary":"This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]","start":103352730,"end":103446177,"strand":-1,"description":"solute carrier family 26 member 5 [Source:HGNC Symbol;Acc:HGNC:9359]"}, {"versioned_ensembl_gene_id":"ENSG00000166164.15","gene_symbol":"BRD7","gene_name":"bromodomain containing 7 [Source:HGNC Symbol;Acc:HGNC:14310]","synonyms":"CELTIX1,BP75","biotype":"protein_coding","ncbi_id":"29117","summary":"This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":50313487,"end":50368934,"strand":-1,"description":"bromodomain containing 7 [Source:HGNC Symbol;Acc:HGNC:14310]"}, {"versioned_ensembl_gene_id":"ENSG00000136826.14","gene_symbol":"KLF4","gene_name":"Kruppel like factor 4 [Source:HGNC Symbol;Acc:HGNC:6348]","synonyms":"GKLF,EZF","biotype":"protein_coding","ncbi_id":"9314","summary":"This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is required for normal development of the barrier function of skin. The encoded protein is thought to control the G1-to-S transition of the cell cycle following DNA damage by mediating the tumor suppressor gene p53. Mice lacking this gene have a normal appearance but lose weight rapidly, and die shortly after birth due to fluid evaporation resulting from compromised epidermal barrier function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":107484852,"end":107490482,"strand":-1,"description":"Kruppel like factor 4 [Source:HGNC Symbol;Acc:HGNC:6348]"}, {"versioned_ensembl_gene_id":"ENSG00000256343.7","gene_symbol":"AC095350.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130651371,"end":130669233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236267.1","gene_symbol":"AP006216.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116813204,"end":116814003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224942.1","gene_symbol":"AL137014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140397062,"end":140398311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203666.12","gene_symbol":"EFCAB2","gene_name":"EF-hand calcium binding domain 2 [Source:HGNC Symbol;Acc:HGNC:28166]","synonyms":"MGC12458,DRC8,CFAP200","biotype":"protein_coding","ncbi_id":"84288","summary":"The gene encodes a protein that contains two EF-hand calcium-binding domains although its function has yet to be determined. Alternatively spliced transcripts have been observed. [provided by RefSeq, Mar 2014]","start":244969705,"end":245127164,"strand":1,"description":"EF-hand calcium binding domain 2 [Source:HGNC Symbol;Acc:HGNC:28166]"}, {"versioned_ensembl_gene_id":"ENSG00000237162.1","gene_symbol":"AC007098.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62939916,"end":62940282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271736.1","gene_symbol":"AL138900.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157280716,"end":157283068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228239.1","gene_symbol":"AL138900.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157232231,"end":157237136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284592.1","gene_symbol":"AL357143.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157203604,"end":157205062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108469.14","gene_symbol":"RECQL5","gene_name":"RecQ like helicase 5 [Source:HGNC Symbol;Acc:HGNC:9950]","synonyms":"RecQ5,FLJ90603","biotype":"protein_coding","ncbi_id":"9400","summary":"The protein encoded by this gene is a helicase that is important for genome stability. The encoded protein also prevents aberrant homologous recombination by displacing RAD51 from ssDNA. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":75626845,"end":75667189,"strand":-1,"description":"RecQ like helicase 5 [Source:HGNC Symbol;Acc:HGNC:9950]"}, {"versioned_ensembl_gene_id":"ENSG00000217178.1","gene_symbol":"AL357563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74282266,"end":74282660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229582.3","gene_symbol":"AL358074.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":125743754,"end":125746552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143382.14","gene_symbol":"ADAMTSL4","gene_name":"ADAMTS like 4 [Source:HGNC Symbol;Acc:HGNC:19706]","synonyms":"TSRC1,DKFZP434K1772","biotype":"protein_coding","ncbi_id":"54507","summary":"This gene is a member of ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs)-like gene family and encodes a protein with seven thrombospondin type 1 repeats. The thrombospondin type 1 repeat domain is found in many proteins with diverse biological functions including cellular adhesion, angiogenesis, and patterning of the developing nervous system. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Sep 2014]","start":150549369,"end":150560937,"strand":1,"description":"ADAMTS like 4 [Source:HGNC Symbol;Acc:HGNC:19706]"}, {"versioned_ensembl_gene_id":"ENSG00000253159.2","gene_symbol":"PCDHGA12","gene_name":"protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:HGNC:8699]","synonyms":"PCDH-GAMMA-A12,KIAA0588,FIB3,CDH21","biotype":"protein_coding","ncbi_id":"26025","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141430589,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:HGNC:8699]"}, {"versioned_ensembl_gene_id":"ENSG00000218483.1","gene_symbol":"AL356277.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74610449,"end":74610715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227236.2","gene_symbol":"AL583844.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235614674,"end":235616397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264270.1","gene_symbol":"AC087749.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75683543,"end":75684799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223786.1","gene_symbol":"AL357507.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74069451,"end":74690727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253305.2","gene_symbol":"PCDHGB6","gene_name":"protocadherin gamma subfamily B, 6 [Source:HGNC Symbol;Acc:HGNC:8713]","synonyms":"PCDH-GAMMA-B6","biotype":"protein_coding","ncbi_id":"56100","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141408021,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 6 [Source:HGNC Symbol;Acc:HGNC:8713]"}, {"versioned_ensembl_gene_id":"ENSG00000264829.1","gene_symbol":"AC087749.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75679474,"end":75679967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262209.2","gene_symbol":"PCDHGB3","gene_name":"protocadherin gamma subfamily B, 3 [Source:HGNC Symbol;Acc:HGNC:8710]","synonyms":"PCDH-GAMMA-B3","biotype":"protein_coding","ncbi_id":"56102","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141370264,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 3 [Source:HGNC Symbol;Acc:HGNC:8710]"}, {"versioned_ensembl_gene_id":"ENSG00000143384.12","gene_symbol":"MCL1","gene_name":"MCL1, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:6943]","synonyms":"Mcl-1,BCL2L3","biotype":"protein_coding","ncbi_id":"4170","summary":"This gene encodes an anti-apoptotic protein, which is a member of the Bcl-2 family. Alternative splicing results in multiple transcript variants. The longest gene product (isoform 1) enhances cell survival by inhibiting apoptosis while the alternatively spliced shorter gene products (isoform 2 and isoform 3) promote apoptosis and are death-inducing. [provided by RefSeq, Oct 2010]","start":150574551,"end":150579738,"strand":-1,"description":"MCL1, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:6943]"}, {"versioned_ensembl_gene_id":"ENSG00000235761.2","gene_symbol":"MTCO3P46","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075293","summary":null,"start":235542159,"end":235542390,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]"}, {"versioned_ensembl_gene_id":"ENSG00000203804.4","gene_symbol":"ADAMTSL4-AS1","gene_name":"ADAMTSL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32041]","synonyms":"FLJ45786,C1orf138","biotype":"processed_transcript","ncbi_id":"574406","summary":null,"start":150560202,"end":150574552,"strand":-1,"description":"ADAMTSL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32041]"}, {"versioned_ensembl_gene_id":"ENSG00000234836.7","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"IRT-1,AIF-1,IBA1,Em:AF129756.17","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31597358,"end":31599195,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000224392.1","gene_symbol":"AL935156.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229258,"end":29230188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276399.1","gene_symbol":"FLJ36000","gene_name":"uncharacterized FLJ36000 [Source:NCBI gene;Acc:284124]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284124","summary":null,"start":22406019,"end":22413744,"strand":1,"description":"uncharacterized FLJ36000 [Source:NCBI gene;Acc:284124]"}, {"versioned_ensembl_gene_id":"ENSG00000261934.2","gene_symbol":"PCDHGA9","gene_name":"protocadherin gamma subfamily A, 9 [Source:HGNC Symbol;Acc:HGNC:8707]","synonyms":"PCDH-GAMMA-A9","biotype":"protein_coding","ncbi_id":"56107","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141402932,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 9 [Source:HGNC Symbol;Acc:HGNC:8707]"}, {"versioned_ensembl_gene_id":"ENSG00000122136.13","gene_symbol":"OBP2A","gene_name":"odorant binding protein 2A [Source:HGNC Symbol;Acc:HGNC:23380]","synonyms":"OBP,LCN13,hOBPIIa","biotype":"protein_coding","ncbi_id":"29991","summary":"This gene encodes a small extracellular protein belonging to the lipocalin superfamily. The protein is thought to transport small, hydrophobic, volatile molecules or odorants through the nasal mucus to olfactory receptors, and may also function as a scavenger of highly concentrated or toxic odors. The protein is expressed as a monomer in the nasal mucus, and can bind diverse types of odorants with a higher affinity for aldehydes and fatty acids. This gene and a highly similar family member are located in a cluster of lipocalin genes on chromosome 9. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":135546139,"end":135549969,"strand":1,"description":"odorant binding protein 2A [Source:HGNC Symbol;Acc:HGNC:23380]"}, {"versioned_ensembl_gene_id":"ENSG00000152942.18","gene_symbol":"RAD17","gene_name":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]","synonyms":"RAD17Sp,CCYC,Rad24","biotype":"protein_coding","ncbi_id":"5884","summary":"The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This protein shares strong similarity with DNA replication factor C (RFC), and can form a complex with RFCs. This protein binds to chromatin prior to DNA damage and is phosphorylated by the checkpoint kinase ATR following damage. This protein recruits the RAD1-RAD9-HUS1 checkpoint protein complex onto chromatin after DNA damage, which may be required for its phosphorylation. The phosphorylation of this protein is required for the DNA-damage-induced cell cycle G2 arrest, and is thought to be a critical early event during checkpoint signaling in DNA-damaged cells. Multiple alternatively spliced transcript variants of this gene, which encode four distinct protein isoforms, have been reported. Two pseudogenes, located on chromosomes 7 and 13, have been identified. [provided by RefSeq, Jul 2013]","start":69369293,"end":69414801,"strand":1,"description":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]"}, {"versioned_ensembl_gene_id":"ENSG00000101266.17","gene_symbol":"CSNK2A1","gene_name":"casein kinase 2 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2457]","synonyms":"Cka2,Cka1","biotype":"protein_coding","ncbi_id":"1457","summary":"Casein kinase II is a serine/threonine protein kinase that phosphorylates acidic proteins such as casein. It is involved in various cellular processes, including cell cycle control, apoptosis, and circadian rhythm. The kinase exists as a tetramer and is composed of an alpha, an alpha-prime, and two beta subunits. The alpha subunits contain the catalytic activity while the beta subunits undergo autophosphorylation. The protein encoded by this gene represents the alpha subunit. Multiple transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Apr 2018]","start":473591,"end":543821,"strand":-1,"description":"casein kinase 2 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2457]"}, {"versioned_ensembl_gene_id":"ENSG00000254122.2","gene_symbol":"PCDHGB7","gene_name":"protocadherin gamma subfamily B, 7 [Source:HGNC Symbol;Acc:HGNC:8714]","synonyms":"PCDH-GAMMA-B7,ME6","biotype":"protein_coding","ncbi_id":"56099","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141417645,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 7 [Source:HGNC Symbol;Acc:HGNC:8714]"}, {"versioned_ensembl_gene_id":"ENSG00000280026.1","gene_symbol":"AC005618.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141350109,"end":141350662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253485.2","gene_symbol":"PCDHGA5","gene_name":"protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:HGNC:8703]","synonyms":"PCDH-GAMMA-A5,ME3,CDH-GAMMA-A5","biotype":"protein_coding","ncbi_id":"56110","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141364232,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:HGNC:8703]"}, {"versioned_ensembl_gene_id":"ENSG00000203326.11","gene_symbol":"ZNF525","gene_name":"zinc finger protein 525 [Source:HGNC Symbol;Acc:HGNC:29423]","synonyms":"KIAA1979","biotype":"protein_coding","ncbi_id":"170958","summary":null,"start":53365693,"end":53392217,"strand":1,"description":"zinc finger protein 525 [Source:HGNC Symbol;Acc:HGNC:29423]"}, {"versioned_ensembl_gene_id":"ENSG00000146830.9","gene_symbol":"GIGYF1","gene_name":"GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:HGNC:9126]","synonyms":"GYF1,PERQ1","biotype":"protein_coding","ncbi_id":"64599","summary":"This gene encodes a member of the gyf family of adaptor proteins. The encoded protein contains a gyf protein interaction domain. It binds growth factor receptor bound 10, another adaptor protein that binds activated insulin-like growth factor 1 and insulin receptors and regulates receptor signaling. [provided by RefSeq, Apr 2017]","start":100679507,"end":100689448,"strand":-1,"description":"GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:HGNC:9126]"}, {"versioned_ensembl_gene_id":"ENSG00000271401.1","gene_symbol":"AC010680.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178644717,"end":178645179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283127.1","gene_symbol":"AF146191.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189979902,"end":189982379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000039319.16","gene_symbol":"ZFYVE16","gene_name":"zinc finger FYVE-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20756]","synonyms":"PPP1R69,KIAA0305","biotype":"protein_coding","ncbi_id":"9765","summary":"This gene encodes an endosomal protein that belongs to the FYVE zinc finger family of proteins. The encoded protein is thought to regulate membrane trafficking in the endosome. This protein functions as a scaffold protein in the transforming growth factor-beta signaling pathway and is involved in positive and negative feedback regulation of the bone morphogenetic protein signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":80408013,"end":80479350,"strand":1,"description":"zinc finger FYVE-type containing 16 [Source:HGNC Symbol;Acc:HGNC:20756]"}, {"versioned_ensembl_gene_id":"ENSG00000258515.1","gene_symbol":"AL355075.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20451305,"end":20451918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231110.1","gene_symbol":"FO393408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140216035,"end":140216804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081853.14","gene_symbol":"PCDHGA2","gene_name":"protocadherin gamma subfamily A, 2 [Source:HGNC Symbol;Acc:HGNC:8700]","synonyms":"PCDH-GAMMA-A2","biotype":"protein_coding","ncbi_id":"56113","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141338760,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 2 [Source:HGNC Symbol;Acc:HGNC:8700]"}, {"versioned_ensembl_gene_id":"ENSG00000232714.1","gene_symbol":"MTND3P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873185","summary":null,"start":235541759,"end":235542097,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]"}, {"versioned_ensembl_gene_id":"ENSG00000161057.11","gene_symbol":"PSMC2","gene_name":"proteasome 26S subunit, ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9548]","synonyms":"S7,Nbla10058,MSS1","biotype":"protein_coding","ncbi_id":"5701","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. This subunit has been shown to interact with several of the basal transcription factors so, in addition to participation in proteasome functions, this subunit may participate in the regulation of transcription. This subunit may also compete with PSMC3 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2011]","start":103344254,"end":103369395,"strand":1,"description":"proteasome 26S subunit, ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9548]"}, {"versioned_ensembl_gene_id":"ENSG00000233506.2","gene_symbol":"AL929561.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137868,"end":29138804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256064.1","gene_symbol":"AC063926.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130419535,"end":130421019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196417.12","gene_symbol":"ZNF765","gene_name":"zinc finger protein 765 [Source:HGNC Symbol;Acc:HGNC:25092]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91661","summary":null,"start":53389793,"end":53430413,"strand":1,"description":"zinc finger protein 765 [Source:HGNC Symbol;Acc:HGNC:25092]"}, {"versioned_ensembl_gene_id":"ENSG00000240382.3","gene_symbol":"IGKV1-17","gene_name":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]","synonyms":"IGKV117,A30","biotype":"IG_V_gene","ncbi_id":"28937","summary":null,"start":89117342,"end":89117844,"strand":-1,"description":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]"}, {"versioned_ensembl_gene_id":"ENSG00000237643.1","gene_symbol":"AL365226.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70394887,"end":70399417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254473.1","gene_symbol":"AL354920.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83707594,"end":83713378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230707.1","gene_symbol":"AL589987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140091743,"end":140092561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187889.12","gene_symbol":"FYB2","gene_name":"FYN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:27295]","synonyms":"RP4-758N20.2,FLJ43208,C1orf168,ARAP","biotype":"protein_coding","ncbi_id":"199920","summary":null,"start":56718804,"end":56819696,"strand":-1,"description":"FYN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:27295]"}, {"versioned_ensembl_gene_id":"ENSG00000240864.3","gene_symbol":"IGKV1-16","gene_name":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]","synonyms":"L1,IGKV116","biotype":"IG_V_gene","ncbi_id":"28938","summary":null,"start":89099859,"end":89100361,"strand":-1,"description":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]"}, {"versioned_ensembl_gene_id":"ENSG00000254372.1","gene_symbol":"AC040914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135455865,"end":135456952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240764.3","gene_symbol":"PCDHGC5","gene_name":"protocadherin gamma subfamily C, 5 [Source:HGNC Symbol;Acc:HGNC:8718]","synonyms":"PCDH-GAMMA-C5","biotype":"protein_coding","ncbi_id":"56097","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141489121,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily C, 5 [Source:HGNC Symbol;Acc:HGNC:8718]"}, {"versioned_ensembl_gene_id":"ENSG00000250684.4","gene_symbol":"ADI1P2","gene_name":"acireductone dioxygenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288971","summary":null,"start":102688317,"end":102688906,"strand":-1,"description":"acireductone dioxygenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52340]"}, {"versioned_ensembl_gene_id":"ENSG00000233145.1","gene_symbol":"AL589987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140017268,"end":140018037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163900.10","gene_symbol":"TMEM41A","gene_name":"transmembrane protein 41A [Source:HGNC Symbol;Acc:HGNC:30544]","synonyms":"MGC15397","biotype":"protein_coding","ncbi_id":"90407","summary":null,"start":185476496,"end":185499057,"strand":-1,"description":"transmembrane protein 41A [Source:HGNC Symbol;Acc:HGNC:30544]"}, {"versioned_ensembl_gene_id":"ENSG00000212215.1","gene_symbol":"RNU6-913P","gene_name":"RNA, U6 small nuclear 913, pseudogene [Source:HGNC Symbol;Acc:HGNC:47876]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481467","summary":null,"start":61664145,"end":61664239,"strand":-1,"description":"RNA, U6 small nuclear 913, pseudogene [Source:HGNC Symbol;Acc:HGNC:47876]"}, {"versioned_ensembl_gene_id":"ENSG00000265735.2","gene_symbol":"RN7SL5P","gene_name":"RNA, 7SL, cytoplasmic 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10040]","synonyms":"RN7SLP2,RN7SL249P,7LEM1","biotype":"misc_RNA","ncbi_id":"6031","summary":null,"start":9442060,"end":9442380,"strand":1,"description":"RNA, 7SL, cytoplasmic 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10040]"}, {"versioned_ensembl_gene_id":"ENSG00000112164.5","gene_symbol":"GLP1R","gene_name":"glucagon like peptide 1 receptor [Source:HGNC Symbol;Acc:HGNC:4324]","synonyms":"GLP-1R","biotype":"protein_coding","ncbi_id":"2740","summary":"This gene encodes a 7-transmembrane protein that functions as a receptor for glucagon-like peptide 1 (GLP-1) hormone, which stimulates glucose-induced insulin secretion. This receptor, which functions at the cell surface, becomes internalized in response to GLP-1 and GLP-1 analogs, and it plays an important role in the signaling cascades leading to insulin secretion. It also displays neuroprotective effects in animal models. Polymorphisms in this gene are associated with diabetes. The protein is an important drug target for the treatment of type 2 diabetes and stroke. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":39048798,"end":39087743,"strand":1,"description":"glucagon like peptide 1 receptor [Source:HGNC Symbol;Acc:HGNC:4324]"}, {"versioned_ensembl_gene_id":"ENSG00000260586.1","gene_symbol":"AC064799.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71342324,"end":71348471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278408.1","gene_symbol":"AC108861.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71547280,"end":71549832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120868.13","gene_symbol":"APAF1","gene_name":"apoptotic peptidase activating factor 1 [Source:HGNC Symbol;Acc:HGNC:576]","synonyms":"CED4,APAF-1","biotype":"protein_coding","ncbi_id":"317","summary":"This gene encodes a cytoplasmic protein that initiates apoptosis. This protein contains several copies of the WD-40 domain, a caspase recruitment domain (CARD), and an ATPase domain (NB-ARC). Upon binding cytochrome c and dATP, this protein forms an oligomeric apoptosome. The apoptosome binds and cleaves caspase 9 preproprotein, releasing its mature, activated form. Activated caspase 9 stimulates the subsequent caspase cascade that commits the cell to apoptosis. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":98645141,"end":98735433,"strand":1,"description":"apoptotic peptidase activating factor 1 [Source:HGNC Symbol;Acc:HGNC:576]"}, {"versioned_ensembl_gene_id":"ENSG00000233533.1","gene_symbol":"MKNK2P1","gene_name":"MAP kinase interacting serine/threonine kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389948","summary":null,"start":36944111,"end":36944738,"strand":-1,"description":"MAP kinase interacting serine/threonine kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44970]"}, {"versioned_ensembl_gene_id":"ENSG00000225362.8","gene_symbol":"CT62","gene_name":"cancer/testis antigen 62 [Source:HGNC Symbol;Acc:HGNC:27286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"196993","summary":null,"start":71110244,"end":71115494,"strand":-1,"description":"cancer/testis antigen 62 [Source:HGNC Symbol;Acc:HGNC:27286]"}, {"versioned_ensembl_gene_id":"ENSG00000260625.2","gene_symbol":"AC026471.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31508471,"end":31509256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259781.1","gene_symbol":"HMGB1P6","gene_name":"high mobility group box 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:4998]","synonyms":"HMGB1L6,HMG1L6","biotype":"processed_pseudogene","ncbi_id":"645292","summary":null,"start":71164770,"end":71165415,"strand":-1,"description":"high mobility group box 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:4998]"}, {"versioned_ensembl_gene_id":"ENSG00000212664.5","gene_symbol":"AC064799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71341158,"end":71341712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135018.13","gene_symbol":"UBQLN1","gene_name":"ubiquilin 1 [Source:HGNC Symbol;Acc:HGNC:12508]","synonyms":"DA41,XDRP1,PLIC-1,DSK2","biotype":"protein_coding","ncbi_id":"29979","summary":"This gene encodes an ubiquitin-like protein (ubiquilin) that shares a high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain an N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically associate with both proteasomes and ubiquitin ligases, and thus are thought to functionally link the ubiquitination machinery to the proteasome to affect in vivo protein degradation. This ubiquilin has also been shown to modulate accumulation of presenilin proteins, and it is found in lesions associated with Alzheimer's and Parkinson's disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":83659963,"end":83708203,"strand":-1,"description":"ubiquilin 1 [Source:HGNC Symbol;Acc:HGNC:12508]"}, {"versioned_ensembl_gene_id":"ENSG00000105819.13","gene_symbol":"PMPCB","gene_name":"peptidase, mitochondrial processing beta subunit [Source:HGNC Symbol;Acc:HGNC:9119]","synonyms":"MPPP52,MPPB","biotype":"protein_coding","ncbi_id":"9512","summary":"This gene is a member of the peptidase M16 family and encodes a protein with a zinc-binding motif. This protein is located in the mitochondrial matrix and catalyzes the cleavage of the leader peptides of precursor proteins newly imported into the mitochondria, though it only functions as part of a heterodimeric complex. [provided by RefSeq, Jul 2008]","start":103297422,"end":103329511,"strand":1,"description":"peptidase, mitochondrial processing beta subunit [Source:HGNC Symbol;Acc:HGNC:9119]"}, {"versioned_ensembl_gene_id":"ENSG00000117036.11","gene_symbol":"ETV3","gene_name":"ETS variant 3 [Source:HGNC Symbol;Acc:HGNC:3492]","synonyms":"PE-1","biotype":"protein_coding","ncbi_id":"2117","summary":null,"start":157121191,"end":157138474,"strand":-1,"description":"ETS variant 3 [Source:HGNC Symbol;Acc:HGNC:3492]"}, {"versioned_ensembl_gene_id":"ENSG00000243053.2","gene_symbol":"RPL31P58","gene_name":"ribosomal protein L31 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:35862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271485","summary":null,"start":28802444,"end":28802822,"strand":1,"description":"ribosomal protein L31 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:35862]"}, {"versioned_ensembl_gene_id":"ENSG00000115504.14","gene_symbol":"EHBP1","gene_name":"EH domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29144]","synonyms":"NACSIN,KIAA0903","biotype":"protein_coding","ncbi_id":"23301","summary":"This gene encodes an Eps15 homology domain binding protein. The encoded protein may play a role in endocytic trafficking. A single nucleotide polymorphism in this gene is associated with an aggressive form of prostate cancer. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":62673851,"end":63046487,"strand":1,"description":"EH domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29144]"}, {"versioned_ensembl_gene_id":"ENSG00000250324.2","gene_symbol":"MRPL22P1","gene_name":"mitochondrial ribosomal protein L22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29700]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359738","summary":null,"start":56320719,"end":56321334,"strand":-1,"description":"mitochondrial ribosomal protein L22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29700]"}, {"versioned_ensembl_gene_id":"ENSG00000253953.2","gene_symbol":"PCDHGB4","gene_name":"protocadherin gamma subfamily B, 4 [Source:HGNC Symbol;Acc:HGNC:8711]","synonyms":"PCDH-GAMMA-B4,FIB2,CDH20","biotype":"protein_coding","ncbi_id":"8641","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. This particular family member is expressed in fibroblasts and is thought to play a role in wound healing in response to injury. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141387698,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 4 [Source:HGNC Symbol;Acc:HGNC:8711]"}, {"versioned_ensembl_gene_id":"ENSG00000231609.5","gene_symbol":"AC009501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63043922,"end":63048640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233118.2","gene_symbol":"UBE2V1P8","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724706","summary":null,"start":40942251,"end":40942515,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44893]"}, {"versioned_ensembl_gene_id":"ENSG00000238959.1","gene_symbol":"RNU7-19P","gene_name":"RNA, U7 small nuclear 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:34115]","synonyms":"U7.19","biotype":"snRNA","ncbi_id":"100147767","summary":null,"start":73027808,"end":73027873,"strand":1,"description":"RNA, U7 small nuclear 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:34115]"}, {"versioned_ensembl_gene_id":"ENSG00000265706.1","gene_symbol":"SNORD53B","gene_name":"small nucleolar RNA, C/D box 53B [Source:HGNC Symbol;Acc:HGNC:52229]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617012","summary":null,"start":28927983,"end":28928060,"strand":1,"description":"small nucleolar RNA, C/D box 53B [Source:HGNC Symbol;Acc:HGNC:52229]"}, {"versioned_ensembl_gene_id":"ENSG00000206523.3","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"dJ80I19.2,OR2J1P,hs6M1-4,OR6-5","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100937,"end":29101875,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000206524.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR6-4,OR2B3P","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086195,"end":29087300,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000254083.5","gene_symbol":"LINC01591","gene_name":"long intergenic non-protein coding RNA 1591 [Source:HGNC Symbol;Acc:HGNC:27819]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286094","summary":null,"start":135234131,"end":135299719,"strand":1,"description":"long intergenic non-protein coding RNA 1591 [Source:HGNC Symbol;Acc:HGNC:27819]"}, {"versioned_ensembl_gene_id":"ENSG00000251218.1","gene_symbol":"AC103764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134849935,"end":134881899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124440.15","gene_symbol":"HIF3A","gene_name":"hypoxia inducible factor 3 alpha subunit [Source:HGNC Symbol;Acc:HGNC:15825]","synonyms":"PASD7,MOP7,IPAS,bHLHe17","biotype":"protein_coding","ncbi_id":"64344","summary":"The protein encoded by this gene is the alpha-3 subunit of one of several alpha/beta-subunit heterodimeric transcription factors that regulate many adaptive responses to low oxygen tension (hypoxia). The alpha-3 subunit lacks the transactivation domain found in factors containing either the alpha-1 or alpha-2 subunits. It is thought that factors containing the alpha-3 subunit are negative regulators of hypoxia-inducible gene expression. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2011]","start":46297046,"end":46343433,"strand":1,"description":"hypoxia inducible factor 3 alpha subunit [Source:HGNC Symbol;Acc:HGNC:15825]"}, {"versioned_ensembl_gene_id":"ENSG00000253433.1","gene_symbol":"NCRNA00250","gene_name":"non-protein coding RNA 250 [Source:NCBI gene;Acc:552853]","synonyms":"C8orf24","biotype":"lincRNA","ncbi_id":"552853","summary":null,"start":134838069,"end":134842637,"strand":1,"description":"non-protein coding RNA 250 [Source:NCBI gene;Acc:552853]"}, {"versioned_ensembl_gene_id":"ENSG00000269124.1","gene_symbol":"AC007193.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46320197,"end":46340004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140688.16","gene_symbol":"C16orf58","gene_name":"chromosome 16 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:25848]","synonyms":"FLJ13868","biotype":"protein_coding","ncbi_id":"64755","summary":"This gene encodes a putative transmembrane protein containing a conserved DUF647 domain that may be involved in protein-protein interaction. The encoded protein is related to a plant protein that participates in ultraviolet B light-sensing during root morphogenesis. [provided by RefSeq, Feb 2013]","start":31489471,"end":31509309,"strand":-1,"description":"chromosome 16 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:25848]"}, {"versioned_ensembl_gene_id":"ENSG00000240053.8","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31670167,"end":31673776,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000229638.1","gene_symbol":"RPL4P4","gene_name":"ribosomal protein L4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647276","summary":null,"start":185417495,"end":185418778,"strand":-1,"description":"ribosomal protein L4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36179]"}, {"versioned_ensembl_gene_id":"ENSG00000271045.1","gene_symbol":"NDUFB9P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075233","summary":null,"start":69349936,"end":69350445,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]"}, {"versioned_ensembl_gene_id":"ENSG00000253265.1","gene_symbol":"IGKV2-14","gene_name":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28927","summary":null,"start":89078010,"end":89078784,"strand":-1,"description":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]"}, {"versioned_ensembl_gene_id":"ENSG00000173065.13","gene_symbol":"FAM222B","gene_name":"family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]","synonyms":"FLJ10700,C17orf63","biotype":"protein_coding","ncbi_id":"55731","summary":null,"start":28755978,"end":28855232,"strand":-1,"description":"family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]"}, {"versioned_ensembl_gene_id":"ENSG00000203933.2","gene_symbol":"CXorf66","gene_name":"chromosome X open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33743]","synonyms":"SGPX,RP11-35F15.2","biotype":"protein_coding","ncbi_id":"347487","summary":"The protein encoded by this gene is predicted to be a type I membrane protein, however, its exact function is not known. [provided by RefSeq, Sep 2009]","start":139955725,"end":139965520,"strand":-1,"description":"chromosome X open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33743]"}, {"versioned_ensembl_gene_id":"ENSG00000253939.1","gene_symbol":"AC007991.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39903775,"end":39995248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258021.1","gene_symbol":"AC025259.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51900565,"end":51901336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240184.6","gene_symbol":"PCDHGC3","gene_name":"protocadherin gamma subfamily C, 3 [Source:HGNC Symbol;Acc:HGNC:8716]","synonyms":"PCDH2,PCDH-GAMMA-C3,PC43,PC-43","biotype":"protein_coding","ncbi_id":"5098","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141475947,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily C, 3 [Source:HGNC Symbol;Acc:HGNC:8716]"}, {"versioned_ensembl_gene_id":"ENSG00000265402.1","gene_symbol":"AC011260.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51612639,"end":51613110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113327.16","gene_symbol":"GABRG2","gene_name":"gamma-aminobutyric acid type A receptor gamma2 subunit [Source:HGNC Symbol;Acc:HGNC:4087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2566","summary":"This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammlian brain, where it acts at GABA-A receptors, which are ligand-gated chloride channels. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene have been associated with epilepsy and febrile seizures. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":162000057,"end":162162977,"strand":1,"description":"gamma-aminobutyric acid type A receptor gamma2 subunit [Source:HGNC Symbol;Acc:HGNC:4087]"}, {"versioned_ensembl_gene_id":"ENSG00000228404.1","gene_symbol":"AP001468.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46185079,"end":46188941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232683.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31593261,"end":31593534,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000136110.12","gene_symbol":"CNMD","gene_name":"chondromodulin [Source:HGNC Symbol;Acc:HGNC:17005]","synonyms":"MYETS1,LECT1,CHM1,CHM-I,BRICD3","biotype":"protein_coding","ncbi_id":"11061","summary":"This gene encodes a glycosylated transmembrane protein that is cleaved to form a mature, secreted protein. The N-terminus of the precursor protein shares characteristics with other surfactant proteins and is sometimes called chondrosurfactant protein although no biological activity has yet been defined for it. The C-terminus of the precursor protein contains a 25 kDa mature protein called leukocyte cell-derived chemotaxin-1 or chondromodulin-1. The mature protein promotes chondrocyte growth and inhibits angiogenesis. This gene is expressed in the avascular zone of prehypertrophic cartilage and its expression decreases during chondrocyte hypertrophy and vascular invasion. The mature protein likely plays a role in endochondral bone development by permitting cartilaginous anlagen to be vascularized and replaced by bone. It may be involved also in the broad control of tissue vascularization during development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":52703264,"end":52739812,"strand":-1,"description":"chondromodulin [Source:HGNC Symbol;Acc:HGNC:17005]"}, {"versioned_ensembl_gene_id":"ENSG00000242276.2","gene_symbol":"RPL5P3","gene_name":"ribosomal protein L5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31034]","synonyms":"HsT18216","biotype":"processed_pseudogene","ncbi_id":"400385","summary":null,"start":71063101,"end":71063989,"strand":-1,"description":"ribosomal protein L5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31034]"}, {"versioned_ensembl_gene_id":"ENSG00000276634.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54762712,"end":54778593,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000162409.10","gene_symbol":"PRKAA2","gene_name":"protein kinase AMP-activated catalytic subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9377]","synonyms":"PRKAA,AMPKa2,AMPK","biotype":"protein_coding","ncbi_id":"5563","summary":"The protein encoded by this gene is a catalytic subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. Studies of the mouse counterpart suggest that this catalytic subunit may control whole-body insulin sensitivity and is necessary for maintaining myocardial energy homeostasis during ischemia. [provided by RefSeq, Jul 2008]","start":56645322,"end":56715335,"strand":1,"description":"protein kinase AMP-activated catalytic subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9377]"}, {"versioned_ensembl_gene_id":"ENSG00000107831.12","gene_symbol":"FGF8","gene_name":"fibroblast growth factor 8 [Source:HGNC Symbol;Acc:HGNC:3686]","synonyms":"AIGF","biotype":"protein_coding","ncbi_id":"2253","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008]","start":101770130,"end":101780369,"strand":-1,"description":"fibroblast growth factor 8 [Source:HGNC Symbol;Acc:HGNC:3686]"}, {"versioned_ensembl_gene_id":"ENSG00000274926.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54699775,"end":54714233,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000162910.18","gene_symbol":"MRPL55","gene_name":"mitochondrial ribosomal protein L55 [Source:HGNC Symbol;Acc:HGNC:16686]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128308","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Multiple transcript variants encoding two different isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":228106679,"end":228109312,"strand":-1,"description":"mitochondrial ribosomal protein L55 [Source:HGNC Symbol;Acc:HGNC:16686]"}, {"versioned_ensembl_gene_id":"ENSG00000238077.1","gene_symbol":"NMNAT1P3","gene_name":"NMNAT1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391603","summary":null,"start":190166764,"end":190167651,"strand":1,"description":"NMNAT1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49165]"}, {"versioned_ensembl_gene_id":"ENSG00000277924.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"cl-6,nkat2,nkat2a,nkat2b,p58,CD158B2","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54668491,"end":54683019,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000104852.14","gene_symbol":"SNRNP70","gene_name":"small nuclear ribonucleoprotein U1 subunit 70 [Source:HGNC Symbol;Acc:HGNC:11150]","synonyms":"RPU1,RNPU1Z,U1-70K,SNRP70,Snp1","biotype":"protein_coding","ncbi_id":"6625","summary":null,"start":49085419,"end":49108605,"strand":1,"description":"small nuclear ribonucleoprotein U1 subunit 70 [Source:HGNC Symbol;Acc:HGNC:11150]"}, {"versioned_ensembl_gene_id":"ENSG00000230157.1","gene_symbol":"ATP5G1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]","synonyms":"ATP5GP3","biotype":"processed_pseudogene","ncbi_id":"319136","summary":null,"start":105536861,"end":105537239,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]"}, {"versioned_ensembl_gene_id":"ENSG00000277795.1","gene_symbol":"AC244517.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141259235,"end":141261364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258114.1","gene_symbol":"AC005871.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117425194,"end":117490419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250299.5","gene_symbol":"MRPS31P4","gene_name":"mitochondrial ribosomal protein S31 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42649]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100885866","summary":null,"start":52600119,"end":52637446,"strand":1,"description":"mitochondrial ribosomal protein S31 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42649]"}, {"versioned_ensembl_gene_id":"ENSG00000163931.15","gene_symbol":"TKT","gene_name":"transketolase [Source:HGNC Symbol;Acc:HGNC:11834]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7086","summary":"This gene encodes a thiamine-dependent enzyme which plays a role in the channeling of excess sugar phosphates to glycolysis in the pentose phosphate pathway. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]","start":53224707,"end":53256052,"strand":-1,"description":"transketolase [Source:HGNC Symbol;Acc:HGNC:11834]"}, {"versioned_ensembl_gene_id":"ENSG00000224257.1","gene_symbol":"VWC2L-IT1","gene_name":"VWC2L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41508]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100885780","summary":null,"start":214510196,"end":214536890,"strand":1,"description":"VWC2L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41508]"}, {"versioned_ensembl_gene_id":"ENSG00000177728.16","gene_symbol":"TMEM94","gene_name":"transmembrane protein 94 [Source:HGNC Symbol;Acc:HGNC:28983]","synonyms":"KIAA0195","biotype":"protein_coding","ncbi_id":"9772","summary":null,"start":75441159,"end":75500090,"strand":1,"description":"transmembrane protein 94 [Source:HGNC Symbol;Acc:HGNC:28983]"}, {"versioned_ensembl_gene_id":"ENSG00000132749.10","gene_symbol":"TESMIN","gene_name":"testis expressed metallothionein like protein [Source:HGNC Symbol;Acc:HGNC:7446]","synonyms":"MTL5,CXCDC2","biotype":"protein_coding","ncbi_id":"9633","summary":"Metallothionein proteins are highly conserved low-molecular-weight cysteine-rich proteins that are induced by and bind to heavy metal ions and have no enzymatic activity. They may play a central role in the regulation of cell growth and differentiation and are involved in spermatogenesis. This gene encodes a metallothionein-like protein which has been shown to be expressed differentially in mouse testis and ovary. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68707440,"end":68751564,"strand":-1,"description":"testis expressed metallothionein like protein [Source:HGNC Symbol;Acc:HGNC:7446]"}, {"versioned_ensembl_gene_id":"ENSG00000011304.19","gene_symbol":"PTBP1","gene_name":"polypyrimidine tract binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9583]","synonyms":"PTB4,PTB3,PTB2,PTB-1,PTB,pPTB,HNRPI,HNRNP-I","biotype":"protein_coding","ncbi_id":"5725","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA-binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has four repeats of quasi-RNA recognition motif (RRM) domains that bind RNAs. This protein binds to the intronic polypyrimidine tracts that requires pre-mRNA splicing and acts via the protein degradation ubiquitin-proteasome pathway. It may also promote the binding of U2 snRNP to pre-mRNAs. This protein is localized in the nucleoplasm and it is also detected in the perinucleolar structure. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":797075,"end":812327,"strand":1,"description":"polypyrimidine tract binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9583]"}, {"versioned_ensembl_gene_id":"ENSG00000183305.13","gene_symbol":"MAGEA2B","gene_name":"MAGE family member A2B [Source:HGNC Symbol;Acc:HGNC:19340]","synonyms":"MGC16973,MAGEA2b,MAGEA2,MAGE2","biotype":"protein_coding","ncbi_id":"266740","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. [provided by RefSeq, Jul 2008]","start":152714586,"end":152718607,"strand":1,"description":"MAGE family member A2B [Source:HGNC Symbol;Acc:HGNC:19340]"}, {"versioned_ensembl_gene_id":"ENSG00000201031.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":149094353,"end":149094462,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000172590.18","gene_symbol":"MRPL52","gene_name":"mitochondrial ribosomal protein L52 [Source:HGNC Symbol;Acc:HGNC:16655]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122704","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which has no bacterial homolog. Multiple transcript variants encoding different protein isoforms were identified through sequence analysis. [provided by RefSeq, Jul 2008]","start":22829879,"end":22835037,"strand":1,"description":"mitochondrial ribosomal protein L52 [Source:HGNC Symbol;Acc:HGNC:16655]"}, {"versioned_ensembl_gene_id":"ENSG00000213062.4","gene_symbol":"AL021068.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169486076,"end":169486986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183324.10","gene_symbol":"REC114","gene_name":"REC114 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:25065]","synonyms":"LOC283677,FLJ44083,FLJ36860,FLJ27520,CT147,C15orf60","biotype":"protein_coding","ncbi_id":"283677","summary":"The protein encoded by this gene is orthologous to the mouse meiotic recombination protein REC114, which is involved in DNA double-strand break formation during meiosis. The encoded protein is conserved in most eukaryotes and was first discovered and characterized in yeast. [provided by RefSeq, Feb 2017]","start":73443158,"end":73560014,"strand":1,"description":"REC114 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:25065]"}, {"versioned_ensembl_gene_id":"ENSG00000113212.6","gene_symbol":"PCDHB7","gene_name":"protocadherin beta 7 [Source:HGNC Symbol;Acc:HGNC:8692]","synonyms":"PCDH-BETA7","biotype":"protein_coding","ncbi_id":"56129","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. The transcript for this particular family member uses more than one polyadenylation site. [provided by RefSeq, Jul 2008]","start":141172619,"end":141176383,"strand":1,"description":"protocadherin beta 7 [Source:HGNC Symbol;Acc:HGNC:8692]"}, {"versioned_ensembl_gene_id":"ENSG00000113211.5","gene_symbol":"PCDHB6","gene_name":"protocadherin beta 6 [Source:HGNC Symbol;Acc:HGNC:8691]","synonyms":"PCDH-BETA6","biotype":"protein_coding","ncbi_id":"56130","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. Unlike the alpha and gamma clusters, the transcripts from these genes do not share common 3' exons. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell neural connections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":141150022,"end":141153287,"strand":1,"description":"protocadherin beta 6 [Source:HGNC Symbol;Acc:HGNC:8691]"}, {"versioned_ensembl_gene_id":"ENSG00000125445.10","gene_symbol":"MRPS7","gene_name":"mitochondrial ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:14499]","synonyms":"RPMS7,RP-S7,MRP-S","biotype":"protein_coding","ncbi_id":"51081","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. In the prokaryotic ribosome, the comparable protein is thought to play an essential role in organizing the 3' domain of the 16 S rRNA in the vicinity of the P- and A-sites. Pseudogenes corresponding to this gene are found on chromosomes 8p and 12p. [provided by RefSeq, Jul 2008]","start":75261674,"end":75266373,"strand":1,"description":"mitochondrial ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:14499]"}, {"versioned_ensembl_gene_id":"ENSG00000206526.2","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"dJ25J6.5,C6orf100","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28943865,"end":28944525,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000270562.1","gene_symbol":"AC097634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71584943,"end":71587409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268053.1","gene_symbol":"AC007785.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46111079,"end":46113863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220913.1","gene_symbol":"AL391361.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160905770,"end":160913638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277855.1","gene_symbol":"AC097634.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71581721,"end":71628558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186952.14","gene_symbol":"TMEM232","gene_name":"transmembrane protein 232 [Source:HGNC Symbol;Acc:HGNC:37270]","synonyms":"FLJ43080","biotype":"protein_coding","ncbi_id":"642987","summary":null,"start":110289233,"end":110738956,"strand":-1,"description":"transmembrane protein 232 [Source:HGNC Symbol;Acc:HGNC:37270]"}, {"versioned_ensembl_gene_id":"ENSG00000242094.1","gene_symbol":"FOXP1-IT1","gene_name":"FOXP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41335]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506815","summary":null,"start":71570255,"end":71574457,"strand":-1,"description":"FOXP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41335]"}, {"versioned_ensembl_gene_id":"ENSG00000175283.7","gene_symbol":"DOLK","gene_name":"dolichol kinase [Source:HGNC Symbol;Acc:HGNC:23406]","synonyms":"TMEM15,KIAA1094,DK1","biotype":"protein_coding","ncbi_id":"22845","summary":"The protein encoded by this gene catalyzes the CTP-mediated phosphorylation of dolichol, and is involved in the synthesis of Dol-P-Man, which is an essential glycosyl carrier lipid for C- and O-mannosylation, N- and O-linked glycosylation of proteins, and for the biosynthesis of glycosyl phosphatidylinositol anchors in endoplasmic reticulum. Mutations in this gene are associated with dolichol kinase deficiency.[provided by RefSeq, Apr 2010]","start":128945530,"end":128947619,"strand":-1,"description":"dolichol kinase [Source:HGNC Symbol;Acc:HGNC:23406]"}, {"versioned_ensembl_gene_id":"ENSG00000164024.11","gene_symbol":"METAP1","gene_name":"methionyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:15789]","synonyms":"MetAP1A,MAP1A,KIAA0094","biotype":"protein_coding","ncbi_id":"23173","summary":null,"start":98995620,"end":99062813,"strand":1,"description":"methionyl aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:15789]"}, {"versioned_ensembl_gene_id":"ENSG00000213305.3","gene_symbol":"HNRNPCP6","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421794","summary":null,"start":85020785,"end":85021655,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48817]"}, {"versioned_ensembl_gene_id":"ENSG00000114115.9","gene_symbol":"RBP1","gene_name":"retinol binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9919]","synonyms":"CRBP1,CRBP,CRABP-I,RBPC,CRBPI","biotype":"protein_coding","ncbi_id":"5947","summary":"This gene encodes the carrier protein involved in the transport of retinol (vitamin A alcohol) from the liver storage site to peripheral tissue. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":139517434,"end":139539829,"strand":-1,"description":"retinol binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9919]"}, {"versioned_ensembl_gene_id":"ENSG00000139329.4","gene_symbol":"LUM","gene_name":"lumican [Source:HGNC Symbol;Acc:HGNC:6724]","synonyms":"SLRR2D,LDC","biotype":"protein_coding","ncbi_id":"4060","summary":"This gene encodes a member of the small leucine-rich proteoglycan (SLRP) family that includes decorin, biglycan, fibromodulin, keratocan, epiphycan, and osteoglycin. In these bifunctional molecules, the protein moiety binds collagen fibrils and the highly charged hydrophilic glycosaminoglycans regulate interfibrillar spacings. Lumican is the major keratan sulfate proteoglycan of the cornea but is also distributed in interstitial collagenous matrices throughout the body. Lumican may regulate collagen fibril organization and circumferential growth, corneal transparency, and epithelial cell migration and tissue repair. [provided by RefSeq, Jul 2008]","start":91102629,"end":91111831,"strand":-1,"description":"lumican [Source:HGNC Symbol;Acc:HGNC:6724]"}, {"versioned_ensembl_gene_id":"ENSG00000218213.1","gene_symbol":"FTH1P26","gene_name":"ferritin heavy chain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37644]","synonyms":"FTHL26","biotype":"processed_pseudogene","ncbi_id":"100420303","summary":null,"start":133676729,"end":133677429,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37644]"}, {"versioned_ensembl_gene_id":"ENSG00000088356.5","gene_symbol":"PDRG1","gene_name":"p53 and DNA damage regulated 1 [Source:HGNC Symbol;Acc:HGNC:16119]","synonyms":"dJ310O13.3,C20orf126","biotype":"protein_coding","ncbi_id":"81572","summary":null,"start":31944342,"end":31952092,"strand":-1,"description":"p53 and DNA damage regulated 1 [Source:HGNC Symbol;Acc:HGNC:16119]"}, {"versioned_ensembl_gene_id":"ENSG00000254106.1","gene_symbol":"LINC01848","gene_name":"long intergenic non-protein coding RNA 1848 [Source:HGNC Symbol;Acc:HGNC:52663]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289673","summary":null,"start":109883182,"end":109884751,"strand":1,"description":"long intergenic non-protein coding RNA 1848 [Source:HGNC Symbol;Acc:HGNC:52663]"}, {"versioned_ensembl_gene_id":"ENSG00000114113.6","gene_symbol":"RBP2","gene_name":"retinol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9920]","synonyms":"RBPC2,CRBPII,CRBP2,CRABP-II","biotype":"protein_coding","ncbi_id":"5948","summary":"This gene encodes an abundant protein present in the small intestinal epithelium. It is thought to participate in the uptake and/or intracellular metabolism of vitamin A. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. This protein may also modulate the supply of retinoic acid to the nuclei of endometrial cells during the menstrual cycle. [provided by RefSeq, Aug 2015]","start":139452884,"end":139480747,"strand":-1,"description":"retinol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9920]"}, {"versioned_ensembl_gene_id":"ENSG00000118526.6","gene_symbol":"TCF21","gene_name":"transcription factor 21 [Source:HGNC Symbol;Acc:HGNC:11632]","synonyms":"POD1,bHLHa23","biotype":"protein_coding","ncbi_id":"6943","summary":"TCF21 encodes a transcription factor of the basic helix-loop-helix family. The TCF21 product is mesoderm specific, and expressed in embryonic epicardium, mesenchyme-derived tissues of lung, gut, gonad, and both mesenchymal and glomerular epithelial cells in the kidney. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":133889138,"end":133895553,"strand":1,"description":"transcription factor 21 [Source:HGNC Symbol;Acc:HGNC:11632]"}, {"versioned_ensembl_gene_id":"ENSG00000125207.7","gene_symbol":"PIWIL1","gene_name":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]","synonyms":"PIWI,HIWI,CT80.1","biotype":"protein_coding","ncbi_id":"9271","summary":"This gene encodes a member of the PIWI subfamily of Argonaute proteins, evolutionarily conserved proteins containing both PAZ and Piwi motifs that play important roles in stem cell self-renewal, RNA silencing, and translational regulation in diverse organisms. The encoded protein may play a role as an intrinsic regulator of the self-renewal capacity of germline and hematopoietic stem cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":130337887,"end":130372637,"strand":1,"description":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]"}, {"versioned_ensembl_gene_id":"ENSG00000130635.15","gene_symbol":"COL5A1","gene_name":"collagen type V alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2209]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1289","summary":"This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":134641774,"end":134844843,"strand":1,"description":"collagen type V alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2209]"}, {"versioned_ensembl_gene_id":"ENSG00000239991.1","gene_symbol":"AC092059.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55166910,"end":55175732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140931.19","gene_symbol":"CMTM3","gene_name":"CKLF like MARVEL transmembrane domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19174]","synonyms":"FLJ31762,CKLFSF3,BNAS2","biotype":"protein_coding","ncbi_id":"123920","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants containing different 5' UTRs, but encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":66603874,"end":66613892,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19174]"}, {"versioned_ensembl_gene_id":"ENSG00000269352.1","gene_symbol":"PTOV1-AS2","gene_name":"PTOV1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51284]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928378","summary":null,"start":49856970,"end":49859289,"strand":-1,"description":"PTOV1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51284]"}, {"versioned_ensembl_gene_id":"ENSG00000267053.6","gene_symbol":"AC012617.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36304580,"end":36312668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259219.1","gene_symbol":"AC084855.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99976481,"end":99980774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272907.1","gene_symbol":"AL844539.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837857,"end":28838994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042429.11","gene_symbol":"MED17","gene_name":"mediator complex subunit 17 [Source:HGNC Symbol;Acc:HGNC:2375]","synonyms":"TRAP80,SRB4,DRIP80,CRSP77,CRSP6","biotype":"protein_coding","ncbi_id":"9440","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008]","start":93784227,"end":93814963,"strand":1,"description":"mediator complex subunit 17 [Source:HGNC Symbol;Acc:HGNC:2375]"}, {"versioned_ensembl_gene_id":"ENSG00000162775.14","gene_symbol":"RBM15","gene_name":"RNA binding motif protein 15 [Source:HGNC Symbol;Acc:HGNC:14959]","synonyms":"OTT1,OTT","biotype":"protein_coding","ncbi_id":"64783","summary":"Members of the SPEN (Split-end) family of proteins, including RBM15, have repressor function in several signaling pathways and may bind to RNA through interaction with spliceosome components (Hiriart et al., 2005 [PubMed 16129689]).[supplied by OMIM, Feb 2009]","start":110338506,"end":110346681,"strand":1,"description":"RNA binding motif protein 15 [Source:HGNC Symbol;Acc:HGNC:14959]"}, {"versioned_ensembl_gene_id":"ENSG00000235458.1","gene_symbol":"CR753818.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745766,"end":29745990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258469.1","gene_symbol":"CHMP4BP1","gene_name":"charged multivesicular body protein 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100307126","summary":null,"start":55298644,"end":55299231,"strand":1,"description":"charged multivesicular body protein 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43616]"}, {"versioned_ensembl_gene_id":"ENSG00000283412.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":87648489,"end":87648549,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000254715.3","gene_symbol":"OR7E154P","gene_name":"olfactory receptor family 7 subfamily E member 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:31309]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403296","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7705182,"end":7706113,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:31309]"}, {"versioned_ensembl_gene_id":"ENSG00000196357.11","gene_symbol":"ZNF565","gene_name":"zinc finger protein 565 [Source:HGNC Symbol;Acc:HGNC:26726]","synonyms":"FLJ36991","biotype":"protein_coding","ncbi_id":"147929","summary":null,"start":36182060,"end":36246257,"strand":-1,"description":"zinc finger protein 565 [Source:HGNC Symbol;Acc:HGNC:26726]"}, {"versioned_ensembl_gene_id":"ENSG00000179862.6","gene_symbol":"CITED4","gene_name":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4 [Source:HGNC Symbol;Acc:HGNC:18696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163732","summary":"The protein encoded by this intronless gene belongs to the CITED family of transcriptional coactivators that bind to several proteins, including CREB-binding protein (CBP) and p300, via a conserved 32 aa C-terminal motif, and regulate gene transcription. This protein also interacts with transcription factor AP2 (TFAP2), and thus may function as a co-activator for TFAP2. Hypermethylation and transcriptional downregulation of this gene has been observed in oligodendroglial tumors with deletions of chromosomal arms 1p and 19q, and associated with longer recurrence-free and overall survival of patients with oligodendroglial tumors. [provided by RefSeq, Aug 2011]","start":40861051,"end":40862366,"strand":-1,"description":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4 [Source:HGNC Symbol;Acc:HGNC:18696]"}, {"versioned_ensembl_gene_id":"ENSG00000218586.3","gene_symbol":"AC006971.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54933699,"end":54938184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187800.13","gene_symbol":"PEAR1","gene_name":"platelet endothelial aggregation receptor 1 [Source:HGNC Symbol;Acc:HGNC:33631]","synonyms":"MEGF12,JEDI,FLJ00193","biotype":"protein_coding","ncbi_id":"375033","summary":"PEAR1 is a platelet receptor that signals upon the formation of platelet-platelet contacts independent of platelet activation and secondary to platelet aggregation (Nanda et al., 2005 [PubMed 15851471]).[supplied by OMIM, Mar 2008]","start":156893698,"end":156916434,"strand":1,"description":"platelet endothelial aggregation receptor 1 [Source:HGNC Symbol;Acc:HGNC:33631]"}, {"versioned_ensembl_gene_id":"ENSG00000249995.1","gene_symbol":"ECM1P2","gene_name":"extracellular matrix protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481698","summary":null,"start":12639086,"end":12641009,"strand":1,"description":"extracellular matrix protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49737]"}, {"versioned_ensembl_gene_id":"ENSG00000223852.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672345,"end":29681055,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000229254.1","gene_symbol":"OR8C1P","gene_name":"olfactory receptor family 8 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8478]","synonyms":"OR912-45,OR912-106,OR8C4P,OR8C3P,OR11-175","biotype":"unprocessed_pseudogene","ncbi_id":"8580","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124376877,"end":124377801,"strand":-1,"description":"olfactory receptor family 8 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8478]"}, {"versioned_ensembl_gene_id":"ENSG00000144115.16","gene_symbol":"THNSL2","gene_name":"threonine synthase like 2 [Source:HGNC Symbol;Acc:HGNC:25602]","synonyms":"TSH2,SOFAT,FLJ10916","biotype":"protein_coding","ncbi_id":"55258","summary":"This gene encodes a threonine synthase-like protein. A similar enzyme in mouse can catalyze the degradation of O-phospho-homoserine to a-ketobutyrate, phosphate, and ammonia. This protein also has phospho-lyase activity on both gamma and beta phosphorylated substrates. In mouse an alternatively spliced form of this protein has been shown to act as a cytokine and can induce the production of the inflammatory cytokine IL6 in osteoblasts. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":88170295,"end":88186636,"strand":1,"description":"threonine synthase like 2 [Source:HGNC Symbol;Acc:HGNC:25602]"}, {"versioned_ensembl_gene_id":"ENSG00000198633.10","gene_symbol":"ZNF534","gene_name":"zinc finger protein 534 [Source:HGNC Symbol;Acc:HGNC:26337]","synonyms":"KRBO3,FLJ25344","biotype":"protein_coding","ncbi_id":"147658","summary":null,"start":52429187,"end":52452315,"strand":1,"description":"zinc finger protein 534 [Source:HGNC Symbol;Acc:HGNC:26337]"}, {"versioned_ensembl_gene_id":"ENSG00000205495.1","gene_symbol":"OR52J3","gene_name":"olfactory receptor family 52 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14799]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119679","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5046526,"end":5047461,"strand":1,"description":"olfactory receptor family 52 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14799]"}, {"versioned_ensembl_gene_id":"ENSG00000254364.1","gene_symbol":"AP000424.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100492528,"end":100493713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235485.1","gene_symbol":"AL021877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34589085,"end":34591278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237770.2","gene_symbol":"SPATA31D2P","gene_name":"SPATA31 subfamily D member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38607]","synonyms":"FAM75D2P","biotype":"unprocessed_pseudogene","ncbi_id":"100130636","summary":null,"start":81966564,"end":81972130,"strand":1,"description":"SPATA31 subfamily D member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38607]"}, {"versioned_ensembl_gene_id":"ENSG00000126787.12","gene_symbol":"DLGAP5","gene_name":"DLG associated protein 5 [Source:HGNC Symbol;Acc:HGNC:16864]","synonyms":"KIAA0008,HURP,DLG7,DLG1","biotype":"protein_coding","ncbi_id":"9787","summary":null,"start":55148112,"end":55191678,"strand":-1,"description":"DLG associated protein 5 [Source:HGNC Symbol;Acc:HGNC:16864]"}, {"versioned_ensembl_gene_id":"ENSG00000265289.1","gene_symbol":"AC104996.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30059339,"end":30065677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223458.2","gene_symbol":"LMO7DN-IT1","gene_name":"LMO7DN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49790]","synonyms":"TCONS_00021569,C13orf45-IT1","biotype":"sense_intronic","ncbi_id":"104326189","summary":null,"start":75876886,"end":75881127,"strand":1,"description":"LMO7DN intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49790]"}, {"versioned_ensembl_gene_id":"ENSG00000261535.1","gene_symbol":"AC005086.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102153355,"end":102154463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177338.13","gene_symbol":"LINC00469","gene_name":"long intergenic non-protein coding RNA 469 [Source:HGNC Symbol;Acc:HGNC:26863]","synonyms":"C17orf54,FLJ40319","biotype":"lincRNA","ncbi_id":"283982","summary":null,"start":73750330,"end":73828520,"strand":-1,"description":"long intergenic non-protein coding RNA 469 [Source:HGNC Symbol;Acc:HGNC:26863]"}, {"versioned_ensembl_gene_id":"ENSG00000176884.14","gene_symbol":"GRIN1","gene_name":"glutamate ionotropic receptor NMDA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4584]","synonyms":"NMDAR1,GluN1","biotype":"protein_coding","ncbi_id":"2902","summary":"The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]","start":137138390,"end":137168762,"strand":1,"description":"glutamate ionotropic receptor NMDA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4584]"}, {"versioned_ensembl_gene_id":"ENSG00000186150.4","gene_symbol":"UBL4B","gene_name":"ubiquitin like 4B [Source:HGNC Symbol;Acc:HGNC:32309]","synonyms":"FLJ25690","biotype":"protein_coding","ncbi_id":"164153","summary":null,"start":110112468,"end":110113945,"strand":1,"description":"ubiquitin like 4B [Source:HGNC Symbol;Acc:HGNC:32309]"}, {"versioned_ensembl_gene_id":"ENSG00000259744.1","gene_symbol":"AC009269.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70848883,"end":70849770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143816.7","gene_symbol":"WNT9A","gene_name":"Wnt family member 9A [Source:HGNC Symbol;Acc:HGNC:12778]","synonyms":"WNT14","biotype":"protein_coding","ncbi_id":"7483","summary":"The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is expressed in gastric cancer cell lines. The protein encoded by this gene shows 75% amino acid identity to chicken Wnt14, which has been shown to play a central role in initiating synovial joint formation in the chick limb. This gene is clustered with another family member, WNT3A, in the chromosome 1q42 region. [provided by RefSeq, Jul 2008]","start":227918656,"end":227947898,"strand":-1,"description":"Wnt family member 9A [Source:HGNC Symbol;Acc:HGNC:12778]"}, {"versioned_ensembl_gene_id":"ENSG00000224346.1","gene_symbol":"BICD1P1","gene_name":"BICD cargo adaptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391472","summary":null,"start":200844240,"end":200845461,"strand":1,"description":"BICD cargo adaptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51374]"}, {"versioned_ensembl_gene_id":"ENSG00000260031.1","gene_symbol":"RPL10P14","gene_name":"ribosomal protein L10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390729","summary":null,"start":50151280,"end":50151577,"strand":-1,"description":"ribosomal protein L10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43897]"}, {"versioned_ensembl_gene_id":"ENSG00000226416.1","gene_symbol":"MRPL23-AS1","gene_name":"MRPL23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42812]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100133545","summary":null,"start":1983237,"end":1989920,"strand":-1,"description":"MRPL23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42812]"}, {"versioned_ensembl_gene_id":"ENSG00000239886.5","gene_symbol":"KRTAP9-2","gene_name":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]","synonyms":"KAP9.2","biotype":"protein_coding","ncbi_id":"83899","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41226648,"end":41227652,"strand":1,"description":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]"}, {"versioned_ensembl_gene_id":"ENSG00000237950.1","gene_symbol":"AL357079.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43944370,"end":43946551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183148.6","gene_symbol":"ANKRD20A2","gene_name":"ankyrin repeat domain 20 family member A2 [Source:HGNC Symbol;Acc:HGNC:31979]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441430","summary":null,"start":40223285,"end":40266392,"strand":1,"description":"ankyrin repeat domain 20 family member A2 [Source:HGNC Symbol;Acc:HGNC:31979]"}, {"versioned_ensembl_gene_id":"ENSG00000223839.7","gene_symbol":"FAM95B1","gene_name":"family with sequence similarity 95 member B1 [Source:HGNC Symbol;Acc:HGNC:32318]","synonyms":"DKFZp686P0734","biotype":"lincRNA","ncbi_id":"100133036","summary":null,"start":40321299,"end":40329221,"strand":1,"description":"family with sequence similarity 95 member B1 [Source:HGNC Symbol;Acc:HGNC:32318]"}, {"versioned_ensembl_gene_id":"ENSG00000162402.13","gene_symbol":"USP24","gene_name":"ubiquitin specific peptidase 24 [Source:HGNC Symbol;Acc:HGNC:12623]","synonyms":"KIAA1057","biotype":"protein_coding","ncbi_id":"23358","summary":"Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP24 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Mar 2008]","start":55066359,"end":55215113,"strand":-1,"description":"ubiquitin specific peptidase 24 [Source:HGNC Symbol;Acc:HGNC:12623]"}, {"versioned_ensembl_gene_id":"ENSG00000254313.1","gene_symbol":"AC090821.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133786093,"end":133786268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172086.7","gene_symbol":"KRCC1","gene_name":"lysine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28039]","synonyms":"FLJ22333","biotype":"protein_coding","ncbi_id":"51315","summary":null,"start":88027205,"end":88055729,"strand":-1,"description":"lysine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28039]"}, {"versioned_ensembl_gene_id":"ENSG00000260973.1","gene_symbol":"AC009021.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22610531,"end":22612196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165606.8","gene_symbol":"DRGX","gene_name":"dorsal root ganglia homeobox [Source:HGNC Symbol;Acc:HGNC:21536]","synonyms":"PRRXL1,DRG11","biotype":"protein_coding","ncbi_id":"644168","summary":null,"start":49364181,"end":49396016,"strand":-1,"description":"dorsal root ganglia homeobox [Source:HGNC Symbol;Acc:HGNC:21536]"}, {"versioned_ensembl_gene_id":"ENSG00000232447.1","gene_symbol":"MTND5P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42034]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873210","summary":null,"start":84521725,"end":84523915,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42034]"}, {"versioned_ensembl_gene_id":"ENSG00000233349.1","gene_symbol":"LINC00333","gene_name":"long intergenic non-protein coding RNA 333 [Source:HGNC Symbol;Acc:HGNC:42050]","synonyms":"NCRNA00333","biotype":"lincRNA","ncbi_id":"100874128","summary":null,"start":84562364,"end":84563236,"strand":1,"description":"long intergenic non-protein coding RNA 333 [Source:HGNC Symbol;Acc:HGNC:42050]"}, {"versioned_ensembl_gene_id":"ENSG00000228597.1","gene_symbol":"MTND4P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873211","summary":null,"start":84520103,"end":84521568,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42035]"}, {"versioned_ensembl_gene_id":"ENSG00000164951.15","gene_symbol":"PDP1","gene_name":"pyruvate dehyrogenase phosphatase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:9279]","synonyms":"PPM2C,PPM2A,PDP,PDH","biotype":"protein_coding","ncbi_id":"54704","summary":"Pyruvate dehydrogenase (E1) is one of the three components (E1, E2, and E3) of the large pyruvate dehydrogenase complex. Pyruvate dehydrogenase kinases catalyze phosphorylation of serine residues of E1 to inactivate the E1 component and inhibit the complex. Pyruvate dehydrogenase phosphatases catalyze the dephosphorylation and activation of the E1 component to reverse the effects of pyruvate dehydrogenase kinases. Pyruvate dehydrogenase phosphatase is a heterodimer consisting of catalytic and regulatory subunits. Two catalytic subunits have been reported; one is predominantly expressed in skeletal muscle and another one is is much more abundant in the liver. The catalytic subunit, encoded by this gene, is the former, and belongs to the protein phosphatase 2C (PP2C) superfamily. Along with the pyruvate dehydrogenase complex and pyruvate dehydrogenase kinases, this enzyme is located in the mitochondrial matrix. Mutation in this gene causes pyruvate dehydrogenase phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Jun 2009]","start":93857807,"end":93926066,"strand":1,"description":"pyruvate dehyrogenase phosphatase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:9279]"}, {"versioned_ensembl_gene_id":"ENSG00000215244.2","gene_symbol":"AL137145.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6277687,"end":6335982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271196.1","gene_symbol":"AC113403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138454540,"end":138454732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234485.5","gene_symbol":"OR7E46P","gene_name":"olfactory receptor family 7 subfamily E member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:8420]","synonyms":"OST379,MCEEP","biotype":"unprocessed_pseudogene","ncbi_id":"402077","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71037685,"end":71038703,"strand":1,"description":"olfactory receptor family 7 subfamily E member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:8420]"}, {"versioned_ensembl_gene_id":"ENSG00000273473.1","gene_symbol":"BX649601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134168769,"end":134169340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187048.12","gene_symbol":"CYP4A11","gene_name":"cytochrome P450 family 4 subfamily A member 11 [Source:HGNC Symbol;Acc:HGNC:2642]","synonyms":"CYP4AII,CYP4A2","biotype":"protein_coding","ncbi_id":"1579","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates medium-chain fatty acids such as laurate and myristate. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":46929177,"end":46941484,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 11 [Source:HGNC Symbol;Acc:HGNC:2642]"}, {"versioned_ensembl_gene_id":"ENSG00000197984.4","gene_symbol":"OR51A8P","gene_name":"olfactory receptor family 51 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15189]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401662","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4830175,"end":4833072,"strand":1,"description":"olfactory receptor family 51 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15189]"}, {"versioned_ensembl_gene_id":"ENSG00000227023.1","gene_symbol":"OR51A3P","gene_name":"olfactory receptor family 51 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14794]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79532","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4937371,"end":4938294,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14794]"}, {"versioned_ensembl_gene_id":"ENSG00000133193.12","gene_symbol":"FAM104A","gene_name":"family with sequence similarity 104 member A [Source:HGNC Symbol;Acc:HGNC:25918]","synonyms":"FLJ14775","biotype":"protein_coding","ncbi_id":"84923","summary":null,"start":73207353,"end":73236753,"strand":-1,"description":"family with sequence similarity 104 member A [Source:HGNC Symbol;Acc:HGNC:25918]"}, {"versioned_ensembl_gene_id":"ENSG00000187021.14","gene_symbol":"PNLIPRP1","gene_name":"pancreatic lipase related protein 1 [Source:HGNC Symbol;Acc:HGNC:9156]","synonyms":"PLRP1","biotype":"protein_coding","ncbi_id":"5407","summary":null,"start":116590385,"end":116609175,"strand":1,"description":"pancreatic lipase related protein 1 [Source:HGNC Symbol;Acc:HGNC:9156]"}, {"versioned_ensembl_gene_id":"ENSG00000243232.4","gene_symbol":"PCDHAC2","gene_name":"protocadherin alpha subfamily C, 2 [Source:HGNC Symbol;Acc:HGNC:8677]","synonyms":"PCDH-ALPHA-C2","biotype":"protein_coding","ncbi_id":"56134","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140966235,"end":141012344,"strand":1,"description":"protocadherin alpha subfamily C, 2 [Source:HGNC Symbol;Acc:HGNC:8677]"}, {"versioned_ensembl_gene_id":"ENSG00000168710.17","gene_symbol":"AHCYL1","gene_name":"adenosylhomocysteinase like 1 [Source:HGNC Symbol;Acc:HGNC:344]","synonyms":"XPVKONA,PPP1R78,IRBIT","biotype":"protein_coding","ncbi_id":"10768","summary":"The protein encoded by this gene interacts with inositol 1,4,5-trisphosphate receptor, type 1 and may be involved in the conversion of S-adenosyl-L-homocysteine to L-homocysteine and adenosine. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":109984686,"end":110023741,"strand":1,"description":"adenosylhomocysteinase like 1 [Source:HGNC Symbol;Acc:HGNC:344]"}, {"versioned_ensembl_gene_id":"ENSG00000104517.12","gene_symbol":"UBR5","gene_name":"ubiquitin protein ligase E3 component n-recognin 5 [Source:HGNC Symbol;Acc:HGNC:16806]","synonyms":"KIAA0896,HYD,EDD1,EDD,DD5","biotype":"protein_coding","ncbi_id":"51366","summary":"This gene encodes a progestin-induced protein, which belongs to the HECT (homology to E6-AP carboxyl terminus) family. The HECT family proteins function as E3 ubiquitin-protein ligases, targeting specific proteins for ubiquitin-mediated proteolysis. This gene is localized to chromosome 8q22 which is disrupted in a variety of cancers. This gene potentially has a role in regulation of cell proliferation or differentiation. [provided by RefSeq, Jul 2008]","start":102253012,"end":102412841,"strand":-1,"description":"ubiquitin protein ligase E3 component n-recognin 5 [Source:HGNC Symbol;Acc:HGNC:16806]"}, {"versioned_ensembl_gene_id":"ENSG00000274294.1","gene_symbol":"AC015660.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99416584,"end":99417204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235831.6","gene_symbol":"BHLHE40-AS1","gene_name":"BHLHE40 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44471]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507582","summary":null,"start":4896809,"end":4979961,"strand":-1,"description":"BHLHE40 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44471]"}, {"versioned_ensembl_gene_id":"ENSG00000227171.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"HZFw1,LIRF","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30060156,"end":30065777,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000275154.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":91714915,"end":91715130,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000147206.16","gene_symbol":"NXF3","gene_name":"nuclear RNA export factor 3 [Source:HGNC Symbol;Acc:HGNC:8073]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56000","summary":"This gene is one member of a family of nuclear RNA export factor genes. Common domain features of this family are a noncanonical RNP-type RNA-binding domain (RBD), 4 leucine-rich repeats (LRRs), a nuclear transport factor 2 (NTF2)-like domain that allows heterodimerization with NTF2-related export protein-1 (NXT1), and a ubiquitin-associated domain that mediates interactions with nucleoporins. The LRRs and NTF2-like domains are required for export activity. Alternative splicing seems to be a common mechanism in this gene family. The encoded protein of this gene has shortened LRR and ubiquitin-associated domains and its RDB is unable to bind RNA. It is located in the nucleoplasm but is not associated with either the nuclear envelope or the nucleolus. [provided by RefSeq, Jul 2008]","start":103075810,"end":103093125,"strand":-1,"description":"nuclear RNA export factor 3 [Source:HGNC Symbol;Acc:HGNC:8073]"}, {"versioned_ensembl_gene_id":"ENSG00000232159.3","gene_symbol":"RAB9BP1","gene_name":"RAB9B, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9793]","synonyms":"RAB9P1","biotype":"processed_pseudogene","ncbi_id":"9366","summary":null,"start":105099473,"end":105100098,"strand":1,"description":"RAB9B, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9793]"}, {"versioned_ensembl_gene_id":"ENSG00000227971.1","gene_symbol":"AC078809.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189645327,"end":189645466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215788.9","gene_symbol":"TNFRSF25","gene_name":"TNF receptor superfamily member 25 [Source:HGNC Symbol;Acc:HGNC:11910]","synonyms":"TNFRSF12,LARD,DR3,DDR3,APO-3,WSL-LR,WSL-1,TRAMP,TR3","biotype":"protein_coding","ncbi_id":"8718","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed preferentially in the tissues enriched in lymphocytes, and it may play a role in regulating lymphocyte homeostasis. This receptor has been shown to stimulate NF-kappa B activity and regulate cell apoptosis. The signal transduction of this receptor is mediated by various death domain containing adaptor proteins. Knockout studies in mice suggested the role of this gene in the removal of self-reactive T cells in the thymus. Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported, most of which are potentially secreted molecules. The alternative splicing of this gene in B and T cells encounters a programmed change upon T-cell activation, which predominantly produces full-length, membrane bound isoforms, and is thought to be involved in controlling lymphocyte proliferation induced by T-cell activation. [provided by RefSeq, Jul 2008]","start":6461151,"end":6466195,"strand":-1,"description":"TNF receptor superfamily member 25 [Source:HGNC Symbol;Acc:HGNC:11910]"}, {"versioned_ensembl_gene_id":"ENSG00000231222.1","gene_symbol":"ARF4P4","gene_name":"ADP ribosylation factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129023","summary":null,"start":80888348,"end":80888867,"strand":1,"description":"ADP ribosylation factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37628]"}, {"versioned_ensembl_gene_id":"ENSG00000185559.13","gene_symbol":"DLK1","gene_name":"delta like non-canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2907]","synonyms":"ZOG,Pref-1,pG2,FA1,Delta1","biotype":"protein_coding","ncbi_id":"8788","summary":"This gene encodes a transmembrane protein that contains multiple epidermal growth factor repeats that functions as a regulator of cell growth. The encoded protein is involved in the differentiation of several cell types including adipocytes. This gene is located in a region of chromosome 14 frequently showing unparental disomy, and is imprinted and expressed from the paternal allele. A single nucleotide variant in this gene is associated with child and adolescent obesity and shows polar overdominance, where heterozygotes carrying an active paternal allele express the phenotype, while mutant homozygotes are normal. [provided by RefSeq, Nov 2015]","start":100725705,"end":100738224,"strand":1,"description":"delta like non-canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2907]"}, {"versioned_ensembl_gene_id":"ENSG00000253564.1","gene_symbol":"AC100823.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73215929,"end":73216627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237898.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.7,dJ25J6.6,HCG16","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28987124,"end":28988405,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000197674.6","gene_symbol":"OR51C1P","gene_name":"olfactory receptor family 51 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15191]","synonyms":"OST734,OR51C3P,OR51C2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401661","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4690423,"end":4697831,"strand":-1,"description":"olfactory receptor family 51 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15191]"}, {"versioned_ensembl_gene_id":"ENSG00000221900.5","gene_symbol":"POM121L12","gene_name":"POM121 transmembrane nucleoporin like 12 [Source:HGNC Symbol;Acc:HGNC:25369]","synonyms":"DKFZp564N2472","biotype":"protein_coding","ncbi_id":"285877","summary":null,"start":53035642,"end":53036924,"strand":1,"description":"POM121 transmembrane nucleoporin like 12 [Source:HGNC Symbol;Acc:HGNC:25369]"}, {"versioned_ensembl_gene_id":"ENSG00000230257.2","gene_symbol":"NFE4","gene_name":"nuclear factor, erythroid 4 [Source:HGNC Symbol;Acc:HGNC:29902]","synonyms":"NF-E4","biotype":"protein_coding","ncbi_id":"58160","summary":"The erythroid-specific protein encoded by this gene, and the ubiquitous transcription factor CP2, form the stage selector protein (SSP) complex, which is involved in preferential expression of the gamma-globin genes in fetal erythroid cells. Alternate use of an in-frame upstream non-AUG (CUG) translation initiation codon, and a downstream AUG codon, results in two isoforms. While the long isoform (22 kDa) acts as an activator, the short isoform (14 kDa) has been shown to repress gamma-globin gene expression. This gene is located in an intron of the FBXL13 gene on the opposite strand. [provided by RefSeq, Jul 2008]","start":102973437,"end":102988856,"strand":1,"description":"nuclear factor, erythroid 4 [Source:HGNC Symbol;Acc:HGNC:29902]"}, {"versioned_ensembl_gene_id":"ENSG00000267361.1","gene_symbol":"AC005495.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69094289,"end":69095499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115484.14","gene_symbol":"CCT4","gene_name":"chaperonin containing TCP1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:1617]","synonyms":"Cctd","biotype":"protein_coding","ncbi_id":"10575","summary":"The chaperonin containing TCP1 (MIM 186980) complex (CCT), also called the TCP1 ring complex, consists of 2 back-to-back rings, each containing 8 unique but homologous subunits, such as CCT4. CCT assists the folding of newly translated polypeptide substrates through multiple rounds of ATP-driven release and rebinding of partially folded intermediate forms. Substrates of CCT include the cytoskeletal proteins actin (see MIM 102560) and tubulin (see MIM 191130), as well as alpha-transducin (MIM 139330) (Won et al., 1998 [PubMed 9819444]).[supplied by OMIM, Mar 2008]","start":61868089,"end":61888804,"strand":-1,"description":"chaperonin containing TCP1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:1617]"}, {"versioned_ensembl_gene_id":"ENSG00000241172.3","gene_symbol":"RN7SL70P","gene_name":"RNA, 7SL, cytoplasmic 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:46086]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479249","summary":null,"start":18957957,"end":18958258,"strand":-1,"description":"RNA, 7SL, cytoplasmic 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:46086]"}, {"versioned_ensembl_gene_id":"ENSG00000207014.1","gene_symbol":"SNORD116-3","gene_name":"small nucleolar RNA, C/D box 116-3 [Source:HGNC Symbol;Acc:HGNC:33069]","synonyms":"HBII-85-3","biotype":"snoRNA","ncbi_id":"100033415","summary":null,"start":25056860,"end":25056954,"strand":1,"description":"small nucleolar RNA, C/D box 116-3 [Source:HGNC Symbol;Acc:HGNC:33069]"}, {"versioned_ensembl_gene_id":"ENSG00000277464.1","gene_symbol":"RN7SL286P","gene_name":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479327","summary":null,"start":32602121,"end":32602411,"strand":1,"description":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]"}, {"versioned_ensembl_gene_id":"ENSG00000139549.2","gene_symbol":"DHH","gene_name":"desert hedgehog [Source:HGNC Symbol;Acc:HGNC:2865]","synonyms":"HHG-3,MGC35145","biotype":"protein_coding","ncbi_id":"50846","summary":"This gene encodes a member of the hedgehog family. The hedgehog gene family encodes signaling molecules that play an important role in regulating morphogenesis. This protein is predicted to be made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the organism. Defects in this protein have been associated with partial gonadal dysgenesis (PGD) accompanied by minifascicular polyneuropathy. This protein may be involved in both male gonadal differentiation and perineurial development. [provided by RefSeq, May 2010]","start":49089421,"end":49094819,"strand":-1,"description":"desert hedgehog [Source:HGNC Symbol;Acc:HGNC:2865]"}, {"versioned_ensembl_gene_id":"ENSG00000284438.1","gene_symbol":"AC018793.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4338660,"end":4339244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284546.1","gene_symbol":"AC018793.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4329865,"end":4330449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257292.2","gene_symbol":"AC117372.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38205098,"end":38206009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272688.1","gene_symbol":"AP005329.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3246401,"end":3247086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227189.2","gene_symbol":"AC092535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1151372,"end":1153701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257173.1","gene_symbol":"AK6P2","gene_name":"adenylate kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51679]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128817","summary":null,"start":38078529,"end":38078999,"strand":-1,"description":"adenylate kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51679]"}, {"versioned_ensembl_gene_id":"ENSG00000182986.12","gene_symbol":"ZNF320","gene_name":"zinc finger protein 320 [Source:HGNC Symbol;Acc:HGNC:13842]","synonyms":"ZFPL,DKFZp686G16228","biotype":"protein_coding","ncbi_id":"162967","summary":"ZNF320 encodes a Kruppel-like zinc finger protein. Members of this protein family are involved in activation or repression of transcription.[supplied by OMIM, Jul 2002]","start":52863790,"end":52897693,"strand":-1,"description":"zinc finger protein 320 [Source:HGNC Symbol;Acc:HGNC:13842]"}, {"versioned_ensembl_gene_id":"ENSG00000255875.2","gene_symbol":"AC008813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52809824,"end":52810708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256338.2","gene_symbol":"RPL41P2","gene_name":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"22970","summary":null,"start":28315651,"end":28316059,"strand":1,"description":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]"}, {"versioned_ensembl_gene_id":"ENSG00000068885.14","gene_symbol":"IFT80","gene_name":"intraflagellar transport 80 [Source:HGNC Symbol;Acc:HGNC:29262]","synonyms":"WDR56,KIAA1374","biotype":"protein_coding","ncbi_id":"57560","summary":"The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]","start":160256986,"end":160399880,"strand":-1,"description":"intraflagellar transport 80 [Source:HGNC Symbol;Acc:HGNC:29262]"}, {"versioned_ensembl_gene_id":"ENSG00000273348.1","gene_symbol":"AC027449.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22347846,"end":22348252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050438.16","gene_symbol":"SLC4A8","gene_name":"solute carrier family 4 member 8 [Source:HGNC Symbol;Acc:HGNC:11034]","synonyms":"NBC3","biotype":"protein_coding","ncbi_id":"9498","summary":"The protein encoded by this gene is a membrane protein that functions to transport sodium and bicarbonate ions across the cell membrane. The encoded protein is important for pH regulation in neurons. The activity of this protein can be inhibited by 4,4'-Di-isothiocyanatostilbene-2,2'-disulfonic acid (DIDS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":51391317,"end":51515763,"strand":1,"description":"solute carrier family 4 member 8 [Source:HGNC Symbol;Acc:HGNC:11034]"}, {"versioned_ensembl_gene_id":"ENSG00000147601.13","gene_symbol":"TERF1","gene_name":"telomeric repeat binding factor 1 [Source:HGNC Symbol;Acc:HGNC:11728]","synonyms":"TRF1,TRF,TRBF1,PIN2","biotype":"protein_coding","ncbi_id":"7013","summary":"This gene encodes a telomere specific protein which is a component of the telomere nucleoprotein complex. This protein is present at telomeres throughout the cell cycle and functions as an inhibitor of telomerase, acting in cis to limit the elongation of individual chromosome ends. The protein structure contains a C-terminal Myb motif, a dimerization domain near its N-terminus and an acidic N-terminus. Two transcripts of this gene are alternatively spliced products. [provided by RefSeq, Jul 2008]","start":73008864,"end":73048122,"strand":1,"description":"telomeric repeat binding factor 1 [Source:HGNC Symbol;Acc:HGNC:11728]"}, {"versioned_ensembl_gene_id":"ENSG00000278193.1","gene_symbol":"AC013562.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72660584,"end":72661470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229612.1","gene_symbol":"SUMO1P2","gene_name":"SUMO1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"474337","summary":null,"start":168898136,"end":168898439,"strand":1,"description":"SUMO1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33149]"}, {"versioned_ensembl_gene_id":"ENSG00000274235.1","gene_symbol":"AC022106.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":150950109,"end":150952460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174547.13","gene_symbol":"MRPL11","gene_name":"mitochondrial ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:14042]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65003","summary":"This nuclear gene encodes a 39S subunit component of the mitochondial ribosome. Alternative splicing results in multiple transcript variants. Pseudogenes for this gene are found on chromosomes 5 and 12. [provided by RefSeq, May 2014]","start":66435075,"end":66466738,"strand":-1,"description":"mitochondrial ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:14042]"}, {"versioned_ensembl_gene_id":"ENSG00000068079.7","gene_symbol":"IFI35","gene_name":"interferon induced protein 35 [Source:HGNC Symbol;Acc:HGNC:5399]","synonyms":"IFP35","biotype":"protein_coding","ncbi_id":"3430","summary":null,"start":43006725,"end":43014456,"strand":1,"description":"interferon induced protein 35 [Source:HGNC Symbol;Acc:HGNC:5399]"}, {"versioned_ensembl_gene_id":"ENSG00000070886.11","gene_symbol":"EPHA8","gene_name":"EPH receptor A8 [Source:HGNC Symbol;Acc:HGNC:3391]","synonyms":"Hek3,EEK","biotype":"protein_coding","ncbi_id":"2046","summary":"This gene encodes a member of the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. The protein encoded by this gene functions as a receptor for ephrin A2, A3 and A5 and plays a role in short-range contact-mediated axonal guidance during development of the mammalian nervous system. [provided by RefSeq, Jul 2008]","start":22563564,"end":22603594,"strand":1,"description":"EPH receptor A8 [Source:HGNC Symbol;Acc:HGNC:3391]"}, {"versioned_ensembl_gene_id":"ENSG00000176472.10","gene_symbol":"ZNF575","gene_name":"zinc finger protein 575 [Source:HGNC Symbol;Acc:HGNC:27606]","synonyms":"FLJ32567","biotype":"protein_coding","ncbi_id":"284346","summary":null,"start":43525497,"end":43536130,"strand":1,"description":"zinc finger protein 575 [Source:HGNC Symbol;Acc:HGNC:27606]"}, {"versioned_ensembl_gene_id":"ENSG00000197619.13","gene_symbol":"ZNF615","gene_name":"zinc finger protein 615 [Source:HGNC Symbol;Acc:HGNC:24740]","synonyms":"FLJ33710","biotype":"protein_coding","ncbi_id":"284370","summary":null,"start":51991332,"end":52008230,"strand":-1,"description":"zinc finger protein 615 [Source:HGNC Symbol;Acc:HGNC:24740]"}, {"versioned_ensembl_gene_id":"ENSG00000255234.5","gene_symbol":"AP000446.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83286128,"end":83423516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267472.1","gene_symbol":"AC005332.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68198921,"end":68199596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257316.1","gene_symbol":"AC087311.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32985838,"end":32987070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253116.1","gene_symbol":"AC027698.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58091442,"end":58106294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204450.7","gene_symbol":"TRIM64","gene_name":"tripartite motif containing 64 [Source:HGNC Symbol;Acc:HGNC:14663]","synonyms":"TRIM64A,C11orf28","biotype":"protein_coding","ncbi_id":"120146","summary":null,"start":89968502,"end":89975228,"strand":1,"description":"tripartite motif containing 64 [Source:HGNC Symbol;Acc:HGNC:14663]"}, {"versioned_ensembl_gene_id":"ENSG00000235455.1","gene_symbol":"IQCF5-AS1","gene_name":"IQCF5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41297]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928999","summary":null,"start":51873596,"end":51875767,"strand":1,"description":"IQCF5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41297]"}, {"versioned_ensembl_gene_id":"ENSG00000053900.10","gene_symbol":"ANAPC4","gene_name":"anaphase promoting complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:19990]","synonyms":"APC4","biotype":"protein_coding","ncbi_id":"29945","summary":"A large protein complex, termed the anaphase-promoting complex (APC), or the cyclosome, promotes metaphase-anaphase transition by ubiquitinating its specific substrates such as mitotic cyclins and anaphase inhibitor, which are subsequently degraded by the 26S proteasome. Biochemical studies have shown that the vertebrate APC contains eight subunits. The composition of the APC is highly conserved in organisms from yeast to humans. The exact function of this gene product is not known. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":25377213,"end":25418498,"strand":1,"description":"anaphase promoting complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:19990]"}, {"versioned_ensembl_gene_id":"ENSG00000219085.1","gene_symbol":"NPM1P37","gene_name":"nucleophosmin 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45216]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422261","summary":null,"start":69705287,"end":69706160,"strand":-1,"description":"nucleophosmin 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45216]"}, {"versioned_ensembl_gene_id":"ENSG00000269825.1","gene_symbol":"AC022150.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52650437,"end":52653284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093010.13","gene_symbol":"COMT","gene_name":"catechol-O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:2228]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1312","summary":"Catechol-O-methyltransferase catalyzes the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine. This O-methylation results in one of the major degradative pathways of the catecholamine transmitters. In addition to its role in the metabolism of endogenous substances, COMT is important in the metabolism of catechol drugs used in the treatment of hypertension, asthma, and Parkinson disease. COMT is found in two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). The differences between S-COMT and MB-COMT reside within the N-termini. Several transcript variants are formed through the use of alternative translation initiation sites and promoters. [provided by RefSeq, Sep 2008]","start":19941607,"end":19969975,"strand":1,"description":"catechol-O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:2228]"}, {"versioned_ensembl_gene_id":"ENSG00000136931.9","gene_symbol":"NR5A1","gene_name":"nuclear receptor subfamily 5 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7983]","synonyms":"SF-1,hSF-1,FTZF1,FTZ1,ELP,AD4BP","biotype":"protein_coding","ncbi_id":"2516","summary":"The protein encoded by this gene is a transcriptional activator involved in sex determination. The encoded protein binds DNA as a monomer. Defects in this gene are a cause of XY sex reversal with or without adrenal failure as well as adrenocortical insufficiency without ovarian defect. [provided by RefSeq, Jul 2008]","start":124481236,"end":124507430,"strand":-1,"description":"nuclear receptor subfamily 5 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7983]"}, {"versioned_ensembl_gene_id":"ENSG00000223833.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31579641,"end":31583730,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000063180.8","gene_symbol":"CA11","gene_name":"carbonic anhydrase 11 [Source:HGNC Symbol;Acc:HGNC:1370]","synonyms":"CARPX1,CARP2","biotype":"protein_coding","ncbi_id":"770","summary":" Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA XI is likely a secreted protein, however, radical changes at active site residues completely conserved in CA isozymes with catalytic activity, make it unlikely that it has carbonic anhydrase activity. It shares properties in common with two other acatalytic CA isoforms, CA VIII and CA X. CA XI is most abundantly expressed in brain, and may play a general role in the central nervous system. [provided by RefSeq, Jul 2008]","start":48637942,"end":48646312,"strand":-1,"description":"carbonic anhydrase 11 [Source:HGNC Symbol;Acc:HGNC:1370]"}, {"versioned_ensembl_gene_id":"ENSG00000188383.8","gene_symbol":"GPAT2P2","gene_name":"glycerol-3-phosphate acyltransferase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52331]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653924","summary":null,"start":97081098,"end":97083249,"strand":1,"description":"glycerol-3-phosphate acyltransferase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52331]"}, {"versioned_ensembl_gene_id":"ENSG00000270983.1","gene_symbol":"AL589674.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142062717,"end":142063053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262445.3","gene_symbol":"AC099684.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1995614,"end":2003671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204670.7","gene_symbol":"IGKV1OR2-3","gene_name":"immunoglobulin kappa variable 1/OR2-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5769]","synonyms":"IGKV1/OR2-3","biotype":"IG_V_pseudogene","ncbi_id":"28866","summary":null,"start":97060128,"end":97060415,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5769]"}, {"versioned_ensembl_gene_id":"ENSG00000236476.2","gene_symbol":"AL593856.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46742329,"end":46743133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065809.13","gene_symbol":"FAM107B","gene_name":"family with sequence similarity 107 member B [Source:HGNC Symbol;Acc:HGNC:23726]","synonyms":"FLJ45505,C10orf45,MGC11034,HITS","biotype":"protein_coding","ncbi_id":"83641","summary":null,"start":14518557,"end":14774897,"strand":-1,"description":"family with sequence similarity 107 member B [Source:HGNC Symbol;Acc:HGNC:23726]"}, {"versioned_ensembl_gene_id":"ENSG00000131471.6","gene_symbol":"AOC3","gene_name":"amine oxidase, copper containing 3 [Source:HGNC Symbol;Acc:HGNC:550]","synonyms":"VAP1,VAP-1,HPAO","biotype":"protein_coding","ncbi_id":"8639","summary":"This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor. The encoded protein is localized to the cell surface, has adhesive properties as well as monoamine oxidase activity, and may be involved in leukocyte trafficking. Alterations in levels of the encoded protein may be associated with many diseases, including diabetes mellitus. A pseudogene of this gene has been described and is located approximately 9-kb downstream on the same chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":42851184,"end":42858130,"strand":1,"description":"amine oxidase, copper containing 3 [Source:HGNC Symbol;Acc:HGNC:550]"}, {"versioned_ensembl_gene_id":"ENSG00000278903.3","gene_symbol":"CU633906.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6318434,"end":6360415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250111.3","gene_symbol":"AC107982.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18835707,"end":18842364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273634.1","gene_symbol":"AC079395.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97008368,"end":97009104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254310.1","gene_symbol":"AC025755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78753596,"end":78753873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248134.1","gene_symbol":"AC079395.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97018343,"end":97018604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254170.1","gene_symbol":"AC008802.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78708734,"end":78716082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264273.1","gene_symbol":"AC107982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18859354,"end":18861466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206948.1","gene_symbol":"SNORA36A","gene_name":"small nucleolar RNA, H/ACA box 36A [Source:HGNC Symbol;Acc:HGNC:32628]","synonyms":"ACA36","biotype":"snoRNA","ncbi_id":"677817","summary":"Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residues U105 and U1244 of 18S rRNA. [provided by RefSeq, Feb 2009]","start":154768528,"end":154768659,"strand":1,"description":"small nucleolar RNA, H/ACA box 36A [Source:HGNC Symbol;Acc:HGNC:32628]"}, {"versioned_ensembl_gene_id":"ENSG00000239967.1","gene_symbol":"OR2A41P","gene_name":"olfactory receptor family 2 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31246]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403234","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144077721,"end":144077825,"strand":1,"description":"olfactory receptor family 2 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31246]"}, {"versioned_ensembl_gene_id":"ENSG00000135905.18","gene_symbol":"DOCK10","gene_name":"dedicator of cytokinesis 10 [Source:HGNC Symbol;Acc:HGNC:23479]","synonyms":"ZIZ3,KIAA0694","biotype":"protein_coding","ncbi_id":"55619","summary":"This gene encodes a member of the dedicator of cytokinesis protein family. Members of this family are guanosine nucleotide exchange factors for Rho GTPases and defined by the presence of conserved DOCK-homology regions. The encoded protein belongs to the D (or Zizimin) subfamily of DOCK proteins, which also contain an N-terminal pleckstrin homology domain. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2014]","start":224765090,"end":225042445,"strand":-1,"description":"dedicator of cytokinesis 10 [Source:HGNC Symbol;Acc:HGNC:23479]"}, {"versioned_ensembl_gene_id":"ENSG00000186431.18","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874248,"end":54890472,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000144188.9","gene_symbol":"TRIM43CP","gene_name":"tripartite motif containing 43C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43981]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643445","summary":null,"start":97025981,"end":97031636,"strand":-1,"description":"tripartite motif containing 43C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43981]"}, {"versioned_ensembl_gene_id":"ENSG00000215154.6","gene_symbol":"AC141586.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":2603350,"end":2630494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248909.1","gene_symbol":"HMGB1P21","gene_name":"high mobility group box 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39106]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419947","summary":null,"start":78644265,"end":78644845,"strand":-1,"description":"high mobility group box 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39106]"}, {"versioned_ensembl_gene_id":"ENSG00000006128.11","gene_symbol":"TAC1","gene_name":"tachykinin precursor 1 [Source:HGNC Symbol;Acc:HGNC:11517]","synonyms":"TAC2,NPK,NKNA","biotype":"protein_coding","ncbi_id":"6863","summary":"This gene encodes four products of the tachykinin peptide hormone family, substance P and neurokinin A, as well as the related peptides, neuropeptide K and neuropeptide gamma. These hormones are thought to function as neurotransmitters which interact with nerve receptors and smooth muscle cells. They are known to induce behavioral responses and function as vasodilators and secretagogues. Substance P is an antimicrobial peptide with antibacterial and antifungal properties. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":97731908,"end":97740472,"strand":1,"description":"tachykinin precursor 1 [Source:HGNC Symbol;Acc:HGNC:11517]"}, {"versioned_ensembl_gene_id":"ENSG00000230343.1","gene_symbol":"AC018892.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97034442,"end":97034706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224552.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"NG26,D6S82E,BAT5","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31726403,"end":31742871,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000236847.1","gene_symbol":"AC018892.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97035461,"end":97037549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270748.1","gene_symbol":"IGKV2OR2-1","gene_name":"immunoglobulin kappa variable 2/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5805]","synonyms":"IGKV2OR2-1A,IGKV2/OR2-1A,IGKV2/OR2-1","biotype":"IG_V_pseudogene","ncbi_id":"28861","summary":null,"start":97046588,"end":97046891,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5805]"}, {"versioned_ensembl_gene_id":"ENSG00000215444.2","gene_symbol":"AL138807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51734533,"end":51735067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205918.9","gene_symbol":"PDPK2P","gene_name":"3-phosphoinositide dependent protein kinase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653650","summary":null,"start":2616121,"end":2643296,"strand":-1,"description":"3-phosphoinositide dependent protein kinase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49897]"}, {"versioned_ensembl_gene_id":"ENSG00000168646.12","gene_symbol":"AXIN2","gene_name":"axin 2 [Source:HGNC Symbol;Acc:HGNC:904]","synonyms":"MGC126582,DKFZp781B0869","biotype":"protein_coding","ncbi_id":"8313","summary":"The Axin-related protein, Axin2, presumably plays an important role in the regulation of the stability of beta-catenin in the Wnt signaling pathway, like its rodent homologs, mouse conductin/rat axil. In mouse, conductin organizes a multiprotein complex of APC (adenomatous polyposis of the colon), beta-catenin, glycogen synthase kinase 3-beta, and conductin, which leads to the degradation of beta-catenin. Apparently, the deregulation of beta-catenin is an important event in the genesis of a number of malignancies. The AXIN2 gene has been mapped to 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Mutations in this gene have been associated with colorectal cancer with defective mismatch repair. [provided by RefSeq, Jul 2008]","start":65528563,"end":65561647,"strand":-1,"description":"axin 2 [Source:HGNC Symbol;Acc:HGNC:904]"}, {"versioned_ensembl_gene_id":"ENSG00000114268.11","gene_symbol":"PFKFB4","gene_name":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 [Source:HGNC Symbol;Acc:HGNC:8875]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5210","summary":"The protein encoded by this gene is one of four bifunctional kinase/phosphatases that regulate the concentration of the glycolytic byproduct fructose-2,6-bisphosphate (F2,6BP). The encoded protein is highly expressed in cancer cells and is induced by hypoxia. This protein is essential to the survival of cancer cells under conditions of hypoxia, because it increases the amount of F2,6BP and ATP at a time when the cell cannot produce much of them. This finding suggests that this protein may be a good target for disruption in cancer cells, hopefully imperiling their survival. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":48517684,"end":48562015,"strand":-1,"description":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 [Source:HGNC Symbol;Acc:HGNC:8875]"}, {"versioned_ensembl_gene_id":"ENSG00000248563.1","gene_symbol":"RPSAP2","gene_name":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]","synonyms":"LAMR1P2,bA60E24.1","biotype":"processed_pseudogene","ncbi_id":"442181","summary":null,"start":28732818,"end":28733705,"strand":1,"description":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]"}, {"versioned_ensembl_gene_id":"ENSG00000200040.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75928513,"end":75928625,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000198400.11","gene_symbol":"NTRK1","gene_name":"neurotrophic receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:8031]","synonyms":"MTC,TRKA,TRK","biotype":"protein_coding","ncbi_id":"4914","summary":"This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, cognitive disability and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date. [provided by RefSeq, Jul 2008]","start":156815640,"end":156881850,"strand":1,"description":"neurotrophic receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:8031]"}, {"versioned_ensembl_gene_id":"ENSG00000272678.1","gene_symbol":"AC112503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123283593,"end":123283983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011478.11","gene_symbol":"QPCTL","gene_name":"glutaminyl-peptide cyclotransferase like [Source:HGNC Symbol;Acc:HGNC:25952]","synonyms":"FLJ20084","biotype":"protein_coding","ncbi_id":"54814","summary":null,"start":45692483,"end":45703989,"strand":1,"description":"glutaminyl-peptide cyclotransferase like [Source:HGNC Symbol;Acc:HGNC:25952]"}, {"versioned_ensembl_gene_id":"ENSG00000135298.13","gene_symbol":"ADGRB3","gene_name":"adhesion G protein-coupled receptor B3 [Source:HGNC Symbol;Acc:HGNC:945]","synonyms":"KIAA0550,BAI3","biotype":"protein_coding","ncbi_id":"577","summary":"This p53-target gene encodes a brain-specific angiogenesis inhibitor, a seven-span transmembrane protein, and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities, and may also play a role in angiogenesis. [provided by RefSeq, Jul 2008]","start":68635367,"end":69389511,"strand":1,"description":"adhesion G protein-coupled receptor B3 [Source:HGNC Symbol;Acc:HGNC:945]"}, {"versioned_ensembl_gene_id":"ENSG00000173175.14","gene_symbol":"ADCY5","gene_name":"adenylate cyclase 5 [Source:HGNC Symbol;Acc:HGNC:236]","synonyms":"AC5","biotype":"protein_coding","ncbi_id":"111","summary":"This gene encodes a member of the membrane-bound adenylyl cyclase enzymes. Adenylyl cyclases mediate G protein-coupled receptor signaling through the synthesis of the second messenger cAMP. Activity of the encoded protein is stimulated by the Gs alpha subunit of G protein-coupled receptors and is inhibited by protein kinase A, calcium and Gi alpha subunits. Single nucleotide polymorphisms in this gene may be associated with low birth weight and type 2 diabetes. Alternatively spliced transcript variants that encode different isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":123282296,"end":123449758,"strand":-1,"description":"adenylate cyclase 5 [Source:HGNC Symbol;Acc:HGNC:236]"}, {"versioned_ensembl_gene_id":"ENSG00000279057.1","gene_symbol":"AC141586.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2620222,"end":2621794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137486.16","gene_symbol":"ARRB1","gene_name":"arrestin beta 1 [Source:HGNC Symbol;Acc:HGNC:711]","synonyms":"ARR1","biotype":"protein_coding","ncbi_id":"408","summary":"Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. Arrestin beta 1 is a cytosolic protein and acts as a cofactor in the beta-adrenergic receptor kinase (BARK) mediated desensitization of beta-adrenergic receptors. Besides the central nervous system, it is expressed at high levels in peripheral blood leukocytes, and thus the BARK/beta-arrestin system is believed to play a major role in regulating receptor-mediated immune functions. Alternatively spliced transcripts encoding different isoforms of arrestin beta 1 have been described. [provided by RefSeq, Jan 2011]","start":75264182,"end":75351705,"strand":-1,"description":"arrestin beta 1 [Source:HGNC Symbol;Acc:HGNC:711]"}, {"versioned_ensembl_gene_id":"ENSG00000107518.16","gene_symbol":"ATRNL1","gene_name":"attractin like 1 [Source:HGNC Symbol;Acc:HGNC:29063]","synonyms":"KIAA0534,FLJ45344,ALP","biotype":"protein_coding","ncbi_id":"26033","summary":null,"start":115093365,"end":115948992,"strand":1,"description":"attractin like 1 [Source:HGNC Symbol;Acc:HGNC:29063]"}, {"versioned_ensembl_gene_id":"ENSG00000226065.1","gene_symbol":"ZBTB45P2","gene_name":"zinc finger and BTB domain containing 45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49228]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729248","summary":null,"start":110383112,"end":110384642,"strand":1,"description":"zinc finger and BTB domain containing 45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49228]"}, {"versioned_ensembl_gene_id":"ENSG00000119335.16","gene_symbol":"SET","gene_name":"SET nuclear proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10760]","synonyms":"PHAPII,IPP2A2,2PP2A","biotype":"protein_coding","ncbi_id":"6418","summary":"The protein encoded by this gene inhibits acetylation of nucleosomes, especially histone H4, by histone acetylases (HAT). This inhibition is most likely accomplished by masking histone lysines from being acetylated, and the consequence is to silence HAT-dependent transcription. The encoded protein is part of a complex localized to the endoplasmic reticulum but is found in the nucleus and inhibits apoptosis following attack by cytotoxic T lymphocytes. This protein can also enhance DNA replication of the adenovirus genome. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":128683424,"end":128696400,"strand":1,"description":"SET nuclear proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10760]"}, {"versioned_ensembl_gene_id":"ENSG00000143375.14","gene_symbol":"CGN","gene_name":"cingulin [Source:HGNC Symbol;Acc:HGNC:17429]","synonyms":"KIAA1319","biotype":"protein_coding","ncbi_id":"57530","summary":null,"start":151510510,"end":151538692,"strand":1,"description":"cingulin [Source:HGNC Symbol;Acc:HGNC:17429]"}, {"versioned_ensembl_gene_id":"ENSG00000175772.10","gene_symbol":"LINC01106","gene_name":"long intergenic non-protein coding RNA 1106 [Source:HGNC Symbol;Acc:HGNC:26769]","synonyms":"FLJ38359","biotype":"lincRNA","ncbi_id":"151009","summary":null,"start":110375138,"end":110384442,"strand":-1,"description":"long intergenic non-protein coding RNA 1106 [Source:HGNC Symbol;Acc:HGNC:26769]"}, {"versioned_ensembl_gene_id":"ENSG00000182578.13","gene_symbol":"CSF1R","gene_name":"colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:2433]","synonyms":"FMS,CSFR,CD115,C-FMS","biotype":"protein_coding","ncbi_id":"1436","summary":"The protein encoded by this gene is the receptor for colony stimulating factor 1, a cytokine which controls the production, differentiation, and function of macrophages. This receptor mediates most if not all of the biological effects of this cytokine. Ligand binding activates the receptor kinase through a process of oligomerization and transphosphorylation. The encoded protein is a tyrosine kinase transmembrane receptor and member of the CSF1/PDGF receptor family of tyrosine-protein kinases. Mutations in this gene have been associated with a predisposition to myeloid malignancy. The first intron of this gene contains a transcriptionally inactive ribosomal protein L7 processed pseudogene oriented in the opposite direction. Alternative splicing results in multiple transcript variants. Expression of a splice variant from an LTR promoter has been found in Hodgkin lymphoma (HL), HL cell lines and anaplastic large cell lymphoma. [provided by RefSeq, Mar 2017]","start":150053291,"end":150113372,"strand":-1,"description":"colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:2433]"}, {"versioned_ensembl_gene_id":"ENSG00000214646.8","gene_symbol":"AC104758.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":77941442,"end":77944582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241499.1","gene_symbol":"AL132838.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93244010,"end":93244323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011114.14","gene_symbol":"BTBD7","gene_name":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]","synonyms":"FUP1,FLJ10648","biotype":"protein_coding","ncbi_id":"55727","summary":null,"start":93237550,"end":93333092,"strand":-1,"description":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]"}, {"versioned_ensembl_gene_id":"ENSG00000139746.15","gene_symbol":"RBM26","gene_name":"RNA binding motif protein 26 [Source:HGNC Symbol;Acc:HGNC:20327]","synonyms":"ZC3H17,SE70-2,PRO1777,PPP1R132,FLJ20957,C13orf10,ARRS2","biotype":"protein_coding","ncbi_id":"64062","summary":null,"start":79311824,"end":79406477,"strand":-1,"description":"RNA binding motif protein 26 [Source:HGNC Symbol;Acc:HGNC:20327]"}, {"versioned_ensembl_gene_id":"ENSG00000204745.3","gene_symbol":"AC083899.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87125390,"end":87196647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261403.1","gene_symbol":"AC104758.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77954075,"end":77963654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223306.2","gene_symbol":"RNU6-1304P","gene_name":"RNA, U6 small nuclear 1304, pseudogene [Source:HGNC Symbol;Acc:HGNC:48267]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480135","summary":null,"start":225741275,"end":225741380,"strand":1,"description":"RNA, U6 small nuclear 1304, pseudogene [Source:HGNC Symbol;Acc:HGNC:48267]"}, {"versioned_ensembl_gene_id":"ENSG00000274967.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53290640,"end":53290751,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000169896.16","gene_symbol":"ITGAM","gene_name":"integrin subunit alpha M [Source:HGNC Symbol;Acc:HGNC:6149]","synonyms":"MAC-1,CR3A,CD11B","biotype":"protein_coding","ncbi_id":"3684","summary":"This gene encodes the integrin alpha M chain. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as macrophage receptor 1 ('Mac-1'), or inactivated-C3b (iC3b) receptor 3 ('CR3'). The alpha M beta 2 integrin is important in the adherence of neutrophils and monocytes to stimulated endothelium, and also in the phagocytosis of complement coated particles. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":31259990,"end":31332892,"strand":1,"description":"integrin subunit alpha M [Source:HGNC Symbol;Acc:HGNC:6149]"}, {"versioned_ensembl_gene_id":"ENSG00000169733.11","gene_symbol":"RFNG","gene_name":"RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:9974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5986","summary":null,"start":82047902,"end":82051831,"strand":-1,"description":"RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:9974]"}, {"versioned_ensembl_gene_id":"ENSG00000226143.1","gene_symbol":"Z98752.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43549389,"end":43550949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234271.1","gene_symbol":"Z98752.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43523261,"end":43523572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125743.10","gene_symbol":"SNRPD2","gene_name":"small nuclear ribonucleoprotein D2 polypeptide [Source:HGNC Symbol;Acc:HGNC:11159]","synonyms":"SNRPD1,Sm-D2","biotype":"protein_coding","ncbi_id":"6633","summary":"The protein encoded by this gene belongs to the small nuclear ribonucleoprotein core protein family. It is required for pre-mRNA splicing and small nuclear ribonucleoprotein biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":45687454,"end":45692569,"strand":-1,"description":"small nuclear ribonucleoprotein D2 polypeptide [Source:HGNC Symbol;Acc:HGNC:11159]"}, {"versioned_ensembl_gene_id":"ENSG00000277611.1","gene_symbol":"Z98752.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43540171,"end":43569498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258131.1","gene_symbol":"AC007656.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96985656,"end":97185609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279190.1","gene_symbol":"AC007656.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97150081,"end":97154627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184414.2","gene_symbol":"IRS3P","gene_name":"insulin receptor substrate 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:6127]","synonyms":"IRS3L","biotype":"processed_pseudogene","ncbi_id":"442338","summary":null,"start":100570131,"end":100571136,"strand":1,"description":"insulin receptor substrate 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:6127]"}, {"versioned_ensembl_gene_id":"ENSG00000257470.1","gene_symbol":"AC013417.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97024021,"end":97051129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172977.12","gene_symbol":"KAT5","gene_name":"lysine acetyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:5275]","synonyms":"ZC2HC5,TIP60,PLIP,HTATIP1,HTATIP,ESA1,cPLA2","biotype":"protein_coding","ncbi_id":"10524","summary":"The protein encoded by this gene belongs to the MYST family of histone acetyl transferases (HATs) and was originally isolated as an HIV-1 TAT-interactive protein. HATs play important roles in regulating chromatin remodeling, transcription and other nuclear processes by acetylating histone and nonhistone proteins. This protein is a histone acetylase that has a role in DNA repair and apoptosis and is thought to play an important role in signal transduction. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":65711996,"end":65719604,"strand":1,"description":"lysine acetyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:5275]"}, {"versioned_ensembl_gene_id":"ENSG00000266076.1","gene_symbol":"AC004805.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":65538102,"end":65641033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271587.1","gene_symbol":"AC004805.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65644308,"end":65644617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270870.1","gene_symbol":"AC004805.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65654914,"end":65655395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154240.16","gene_symbol":"CEP112","gene_name":"centrosomal protein 112 [Source:HGNC Symbol;Acc:HGNC:28514]","synonyms":"MGC33887,CCDC46","biotype":"protein_coding","ncbi_id":"201134","summary":"This gene encodes a coiled-coil domain containing protein that belongs to the cell division control protein 42 effector protein family. In neurons, it localizes to the cytoplasm of dendrites and is also enriched in the nucleus where it interacts with the RNA polymerase III transcriptional repressor Maf1 to regulate gamma-aminobutyric acid A receptor surface expression. In addition, the protein has been identified as a component of the human centrosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":65635538,"end":66192084,"strand":-1,"description":"centrosomal protein 112 [Source:HGNC Symbol;Acc:HGNC:28514]"}, {"versioned_ensembl_gene_id":"ENSG00000271074.1","gene_symbol":"AC012491.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211104934,"end":211105732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231017.1","gene_symbol":"AC013404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211298941,"end":211299189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187098.14","gene_symbol":"MITF","gene_name":"melanogenesis associated transcription factor [Source:HGNC Symbol;Acc:HGNC:7105]","synonyms":"WS2A,WS2,MI,bHLHe32","biotype":"protein_coding","ncbi_id":"4286","summary":"The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]","start":69739435,"end":69968337,"strand":1,"description":"melanogenesis associated transcription factor [Source:HGNC Symbol;Acc:HGNC:7105]"}, {"versioned_ensembl_gene_id":"ENSG00000233623.2","gene_symbol":"PGAM1P11","gene_name":"phosphoglycerate mutase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42464]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420660","summary":null,"start":10058671,"end":10059648,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42464]"}, {"versioned_ensembl_gene_id":"ENSG00000130939.18","gene_symbol":"UBE4B","gene_name":"ubiquitination factor E4B [Source:HGNC Symbol;Acc:HGNC:12500]","synonyms":"UFD2,UBOX3,KIAA0684,E4","biotype":"protein_coding","ncbi_id":"10277","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes an additional conjugation factor, E4, which is involved in multiubiquitin chain assembly. This gene is also the strongest candidate in the neuroblastoma tumor suppressor genes. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":10032832,"end":10181239,"strand":1,"description":"ubiquitination factor E4B [Source:HGNC Symbol;Acc:HGNC:12500]"}, {"versioned_ensembl_gene_id":"ENSG00000262950.1","gene_symbol":"AC007861.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49442910,"end":49454078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180264.11","gene_symbol":"ADGRD2","gene_name":"adhesion G protein-coupled receptor D2 [Source:HGNC Symbol;Acc:HGNC:18651]","synonyms":"PGR24,GPR144","biotype":"protein_coding","ncbi_id":"347088","summary":null,"start":124451425,"end":124478589,"strand":1,"description":"adhesion G protein-coupled receptor D2 [Source:HGNC Symbol;Acc:HGNC:18651]"}, {"versioned_ensembl_gene_id":"ENSG00000237032.1","gene_symbol":"RPSAP7","gene_name":"ribosomal protein SA pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31461]","synonyms":"LAMR1P7","biotype":"processed_pseudogene","ncbi_id":"654506","summary":null,"start":14723171,"end":14724055,"strand":-1,"description":"ribosomal protein SA pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31461]"}, {"versioned_ensembl_gene_id":"ENSG00000253848.1","gene_symbol":"AC010834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93741193,"end":93744534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207234.1","gene_symbol":"RNU6-125P","gene_name":"RNA, U6 small nuclear 125, pseudogene [Source:HGNC Symbol;Acc:HGNC:47088]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479621","summary":null,"start":88816779,"end":88816885,"strand":1,"description":"RNA, U6 small nuclear 125, pseudogene [Source:HGNC Symbol;Acc:HGNC:47088]"}, {"versioned_ensembl_gene_id":"ENSG00000277615.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000265602.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30122351,"end":30122511,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000202071.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":66003839,"end":66003940,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264370.1","gene_symbol":"MIR3125","gene_name":"microRNA 3125 [Source:HGNC Symbol;Acc:HGNC:38219]","synonyms":"hsa-mir-3125","biotype":"miRNA","ncbi_id":"100422986","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12737367,"end":12737444,"strand":1,"description":"microRNA 3125 [Source:HGNC Symbol;Acc:HGNC:38219]"}, {"versioned_ensembl_gene_id":"ENSG00000252795.1","gene_symbol":"RNU6-56P","gene_name":"RNA, U6 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:42546]","synonyms":"RNU6-56","biotype":"snRNA","ncbi_id":"100873764","summary":null,"start":38779424,"end":38779516,"strand":1,"description":"RNA, U6 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:42546]"}, {"versioned_ensembl_gene_id":"ENSG00000201725.1","gene_symbol":"RNU6-304P","gene_name":"RNA, U6 small nuclear 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:47267]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481275","summary":null,"start":8883427,"end":8883533,"strand":-1,"description":"RNA, U6 small nuclear 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:47267]"}, {"versioned_ensembl_gene_id":"ENSG00000222069.1","gene_symbol":"RN7SKP285","gene_name":"RNA, 7SK small nuclear pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:46009]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480920","summary":null,"start":103523562,"end":103523879,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:46009]"}, {"versioned_ensembl_gene_id":"ENSG00000252017.1","gene_symbol":"RNU6-1194P","gene_name":"RNA, U6 small nuclear 1194, pseudogene [Source:HGNC Symbol;Acc:HGNC:48157]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481557","summary":null,"start":282689,"end":282792,"strand":-1,"description":"RNA, U6 small nuclear 1194, pseudogene [Source:HGNC Symbol;Acc:HGNC:48157]"}, {"versioned_ensembl_gene_id":"ENSG00000275229.1","gene_symbol":"RNU1-68P","gene_name":"RNA, U1 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48410]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481615","summary":null,"start":149700151,"end":149700296,"strand":-1,"description":"RNA, U1 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:48410]"}, {"versioned_ensembl_gene_id":"ENSG00000212485.1","gene_symbol":"RNU6-1197P","gene_name":"RNA, U6 small nuclear 1197, pseudogene [Source:HGNC Symbol;Acc:HGNC:48160]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481558","summary":null,"start":74079537,"end":74079643,"strand":1,"description":"RNA, U6 small nuclear 1197, pseudogene [Source:HGNC Symbol;Acc:HGNC:48160]"}, {"versioned_ensembl_gene_id":"ENSG00000251889.1","gene_symbol":"RNU4-49P","gene_name":"RNA, U4 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:46985]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481187","summary":null,"start":48340687,"end":48340826,"strand":-1,"description":"RNA, U4 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:46985]"}, {"versioned_ensembl_gene_id":"ENSG00000284216.1","gene_symbol":"MIR1909","gene_name":"microRNA 1909 [Source:HGNC Symbol;Acc:HGNC:35393]","synonyms":"MIRN1909,hsa-mir-1909","biotype":"miRNA","ncbi_id":"100302210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1816159,"end":1816238,"strand":-1,"description":"microRNA 1909 [Source:HGNC Symbol;Acc:HGNC:35393]"}, {"versioned_ensembl_gene_id":"ENSG00000266178.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30922332,"end":30922420,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284595.1","gene_symbol":"MIR6785","gene_name":"microRNA 6785 [Source:HGNC Symbol;Acc:HGNC:50206]","synonyms":"hsa-mir-6785","biotype":"miRNA","ncbi_id":"102466911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75498548,"end":75498628,"strand":1,"description":"microRNA 6785 [Source:HGNC Symbol;Acc:HGNC:50206]"}, {"versioned_ensembl_gene_id":"ENSG00000201241.1","gene_symbol":"RNU6-978P","gene_name":"RNA, U6 small nuclear 978, pseudogene [Source:HGNC Symbol;Acc:HGNC:47941]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479998","summary":null,"start":19883614,"end":19883716,"strand":1,"description":"RNA, U6 small nuclear 978, pseudogene [Source:HGNC Symbol;Acc:HGNC:47941]"}, {"versioned_ensembl_gene_id":"ENSG00000207839.1","gene_symbol":"MIR33B","gene_name":"microRNA 33b [Source:HGNC Symbol;Acc:HGNC:32791]","synonyms":"MIRN33B,hsa-mir-33b","biotype":"miRNA","ncbi_id":"693120","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17813836,"end":17813931,"strand":-1,"description":"microRNA 33b [Source:HGNC Symbol;Acc:HGNC:32791]"}, {"versioned_ensembl_gene_id":"ENSG00000206776.1","gene_symbol":"SNORA32","gene_name":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":119388348,"end":119388469,"strand":1,"description":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]"}, {"versioned_ensembl_gene_id":"ENSG00000212618.1","gene_symbol":"snoMBII-202","gene_name":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":18943999,"end":18944073,"strand":1,"description":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]"}, {"versioned_ensembl_gene_id":"ENSG00000276664.1","gene_symbol":"TUG1_1","gene_name":"Taurine upregulated gene 1 conserved region 1 [Source:RFAM;Acc:RF01882]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30971005,"end":30971149,"strand":1,"description":"Taurine upregulated gene 1 conserved region 1 [Source:RFAM;Acc:RF01882]"}, {"versioned_ensembl_gene_id":"ENSG00000199454.1","gene_symbol":"RNA5SP388","gene_name":"RNA, 5S ribosomal pseudogene 388 [Source:HGNC Symbol;Acc:HGNC:43288]","synonyms":"RN5S388","biotype":"rRNA","ncbi_id":"100873642","summary":null,"start":78177803,"end":78177921,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 388 [Source:HGNC Symbol;Acc:HGNC:43288]"}, {"versioned_ensembl_gene_id":"ENSG00000251767.1","gene_symbol":"RNU7-8P","gene_name":"RNA, U7 small nuclear 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:34104]","synonyms":"U7.8,RNU7-139P","biotype":"snRNA","ncbi_id":"100147756","summary":null,"start":77420325,"end":77420386,"strand":1,"description":"RNA, U7 small nuclear 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:34104]"}, {"versioned_ensembl_gene_id":"ENSG00000284494.1","gene_symbol":"AC270306.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179455294,"end":179455974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277014.1","gene_symbol":"MIR3179-4","gene_name":"microRNA 3179-4 [Source:HGNC Symbol;Acc:HGNC:50838]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504729","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18494493,"end":18494576,"strand":-1,"description":"microRNA 3179-4 [Source:HGNC Symbol;Acc:HGNC:50838]"}, {"versioned_ensembl_gene_id":"ENSG00000284532.1","gene_symbol":"MIR4723","gene_name":"microRNA 4723 [Source:HGNC Symbol;Acc:HGNC:41660]","synonyms":"hsa-mir-4723","biotype":"miRNA","ncbi_id":"100616388","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28360654,"end":28360734,"strand":1,"description":"microRNA 4723 [Source:HGNC Symbol;Acc:HGNC:41660]"}, {"versioned_ensembl_gene_id":"ENSG00000284344.1","gene_symbol":"MIR2117","gene_name":"microRNA 2117 [Source:HGNC Symbol;Acc:HGNC:37311]","synonyms":"hsa-mir-2117","biotype":"miRNA","ncbi_id":"100313779","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43444806,"end":43444885,"strand":1,"description":"microRNA 2117 [Source:HGNC Symbol;Acc:HGNC:37311]"}, {"versioned_ensembl_gene_id":"ENSG00000275451.1","gene_symbol":"MIR6085","gene_name":"microRNA 6085 [Source:HGNC Symbol;Acc:HGNC:50002]","synonyms":"hsa-mir-6085","biotype":"miRNA","ncbi_id":"102464834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62343029,"end":62343138,"strand":1,"description":"microRNA 6085 [Source:HGNC Symbol;Acc:HGNC:50002]"}, {"versioned_ensembl_gene_id":"ENSG00000199652.2","gene_symbol":"RNU1-35P","gene_name":"RNA, U1 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48377]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480157","summary":null,"start":135742343,"end":135742495,"strand":-1,"description":"RNA, U1 small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:48377]"}, {"versioned_ensembl_gene_id":"ENSG00000275633.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":54684540,"end":54709099,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000211579.2","gene_symbol":"MIR759","gene_name":"microRNA 759 [Source:HGNC Symbol;Acc:HGNC:37307]","synonyms":"hsa-mir-759","biotype":"miRNA","ncbi_id":"100313778","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52810050,"end":52810140,"strand":1,"description":"microRNA 759 [Source:HGNC Symbol;Acc:HGNC:37307]"}, {"versioned_ensembl_gene_id":"ENSG00000201221.1","gene_symbol":"RNU4-40P","gene_name":"RNA, U4 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46976]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479576","summary":null,"start":35887659,"end":35887801,"strand":1,"description":"RNA, U4 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46976]"}, {"versioned_ensembl_gene_id":"ENSG00000252428.1","gene_symbol":"RNA5SP285","gene_name":"RNA, 5S ribosomal pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:43185]","synonyms":"RN5S285","biotype":"rRNA","ncbi_id":"100873538","summary":null,"start":72299720,"end":72299838,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 285 [Source:HGNC Symbol;Acc:HGNC:43185]"}, {"versioned_ensembl_gene_id":"ENSG00000275524.1","gene_symbol":"SNORD115-26","gene_name":"small nucleolar RNA, C/D box 115-26 [Source:HGNC Symbol;Acc:HGNC:33045]","synonyms":"HBII-52-26","biotype":"snoRNA","ncbi_id":"100033802","summary":null,"start":25218617,"end":25218698,"strand":1,"description":"small nucleolar RNA, C/D box 115-26 [Source:HGNC Symbol;Acc:HGNC:33045]"}, {"versioned_ensembl_gene_id":"ENSG00000252739.1","gene_symbol":"RNU7-151P","gene_name":"RNA, U7 small nuclear 151 pseudogene [Source:HGNC Symbol;Acc:HGNC:45685]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480824","summary":null,"start":102837047,"end":102837099,"strand":-1,"description":"RNA, U7 small nuclear 151 pseudogene [Source:HGNC Symbol;Acc:HGNC:45685]"}, {"versioned_ensembl_gene_id":"ENSG00000284222.1","gene_symbol":"AC113189.11","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7439159,"end":7443327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283591.1","gene_symbol":"MIR4430","gene_name":"microRNA 4430 [Source:HGNC Symbol;Acc:HGNC:41646]","synonyms":"hsa-mir-4430","biotype":"miRNA","ncbi_id":"100616136","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33418516,"end":33418564,"strand":1,"description":"microRNA 4430 [Source:HGNC Symbol;Acc:HGNC:41646]"}, {"versioned_ensembl_gene_id":"ENSG00000206659.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":175022479,"end":175022580,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200237.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":9819954,"end":9820094,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000278036.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":27315120,"end":27315226,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200693.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":63651296,"end":63651499,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000212505.1","gene_symbol":"RNA5SP299","gene_name":"RNA, 5S ribosomal pseudogene 299 [Source:HGNC Symbol;Acc:HGNC:43199]","synonyms":"RN5S299","biotype":"rRNA","ncbi_id":"100873574","summary":null,"start":8656716,"end":8656831,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 299 [Source:HGNC Symbol;Acc:HGNC:43199]"}, {"versioned_ensembl_gene_id":"ENSG00000276753.1","gene_symbol":"MIR6821","gene_name":"microRNA 6821 [Source:HGNC Symbol;Acc:HGNC:49980]","synonyms":"hsa-mir-6821","biotype":"miRNA","ncbi_id":"102465493","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49962866,"end":49962939,"strand":1,"description":"microRNA 6821 [Source:HGNC Symbol;Acc:HGNC:49980]"}, {"versioned_ensembl_gene_id":"ENSG00000239964.3","gene_symbol":"RN7SL748P","gene_name":"RNA, 7SL, cytoplasmic 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:46764]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481125","summary":null,"start":36522191,"end":36522501,"strand":1,"description":"RNA, 7SL, cytoplasmic 748, pseudogene [Source:HGNC Symbol;Acc:HGNC:46764]"}, {"versioned_ensembl_gene_id":"ENSG00000223224.1","gene_symbol":"SNORD71","gene_name":"small nucleolar RNA, C/D box 71 [Source:HGNC Symbol;Acc:HGNC:32732]","synonyms":"MIRN768,hsa-mir-768,HBII-239","biotype":"snoRNA","ncbi_id":"692111","summary":null,"start":71758402,"end":71758487,"strand":-1,"description":"small nucleolar RNA, C/D box 71 [Source:HGNC Symbol;Acc:HGNC:32732]"}, {"versioned_ensembl_gene_id":"ENSG00000284140.1","gene_symbol":"MIR3618","gene_name":"microRNA 3618 [Source:HGNC Symbol;Acc:HGNC:38937]","synonyms":"hsa-mir-3618","biotype":"miRNA","ncbi_id":"100500860","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20085746,"end":20085833,"strand":1,"description":"microRNA 3618 [Source:HGNC Symbol;Acc:HGNC:38937]"}, {"versioned_ensembl_gene_id":"ENSG00000284261.1","gene_symbol":"MIR4657","gene_name":"microRNA 4657 [Source:HGNC Symbol;Acc:HGNC:41706]","synonyms":"hsa-mir-4657","biotype":"miRNA","ncbi_id":"100616393","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44881748,"end":44881800,"strand":-1,"description":"microRNA 4657 [Source:HGNC Symbol;Acc:HGNC:41706]"}, {"versioned_ensembl_gene_id":"ENSG00000207771.1","gene_symbol":"MIR550A1","gene_name":"microRNA 550a-1 [Source:HGNC Symbol;Acc:HGNC:32804]","synonyms":"MIRN550-1,MIR550-1,hsa-mir-550-1","biotype":"miRNA","ncbi_id":"693133","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30289794,"end":30289890,"strand":1,"description":"microRNA 550a-1 [Source:HGNC Symbol;Acc:HGNC:32804]"}, {"versioned_ensembl_gene_id":"ENSG00000254172.1","gene_symbol":"RNU5A-3P","gene_name":"RNA, U5A small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42519]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873831","summary":null,"start":30643689,"end":30643802,"strand":1,"description":"RNA, U5A small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42519]"}, {"versioned_ensembl_gene_id":"ENSG00000199924.1","gene_symbol":"RNU6-1252P","gene_name":"RNA, U6 small nuclear 1252, pseudogene [Source:HGNC Symbol;Acc:HGNC:48215]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480113","summary":null,"start":52494849,"end":52494952,"strand":1,"description":"RNA, U6 small nuclear 1252, pseudogene [Source:HGNC Symbol;Acc:HGNC:48215]"}, {"versioned_ensembl_gene_id":"ENSG00000207142.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42454720,"end":42454821,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222376.1","gene_symbol":"RN7SKP152","gene_name":"RNA, 7SK small nuclear pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:45876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479163","summary":null,"start":166180652,"end":166180966,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:45876]"}, {"versioned_ensembl_gene_id":"ENSG00000222997.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130505106,"end":130505201,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252484.1","gene_symbol":"RN7SKP49","gene_name":"RNA, 7SK small nuclear pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45773]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480848","summary":null,"start":224107282,"end":224107541,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45773]"}, {"versioned_ensembl_gene_id":"ENSG00000242251.3","gene_symbol":"RN7SL20P","gene_name":"RNA, 7SL, cytoplasmic 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46036]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479232","summary":null,"start":31757202,"end":31757498,"strand":1,"description":"RNA, 7SL, cytoplasmic 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46036]"}, {"versioned_ensembl_gene_id":"ENSG00000211574.1","gene_symbol":"MIR770","gene_name":"microRNA 770 [Source:HGNC Symbol;Acc:HGNC:33143]","synonyms":"MIRN770,hsa-mir-770","biotype":"miRNA","ncbi_id":"768222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100852390,"end":100852487,"strand":1,"description":"microRNA 770 [Source:HGNC Symbol;Acc:HGNC:33143]"}, {"versioned_ensembl_gene_id":"ENSG00000283561.1","gene_symbol":"MIR376A2","gene_name":"microRNA 376a-2 [Source:HGNC Symbol;Acc:HGNC:32532]","synonyms":"MIRN376A2,hsa-mir-376a-2","biotype":"miRNA","ncbi_id":"664615","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101040069,"end":101040148,"strand":1,"description":"microRNA 376a-2 [Source:HGNC Symbol;Acc:HGNC:32532]"}, {"versioned_ensembl_gene_id":"ENSG00000221461.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":123180310,"end":123180525,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000242381.3","gene_symbol":"RN7SL741P","gene_name":"RNA, 7SL, cytoplasmic 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:46757]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481124","summary":null,"start":25944478,"end":25944766,"strand":1,"description":"RNA, 7SL, cytoplasmic 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:46757]"}, {"versioned_ensembl_gene_id":"ENSG00000276295.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153721328,"end":153721625,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000243847.3","gene_symbol":"RN7SL610P","gene_name":"RNA, 7SL, cytoplasmic 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:46626]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479444","summary":null,"start":23996795,"end":23997085,"strand":-1,"description":"RNA, 7SL, cytoplasmic 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:46626]"}, {"versioned_ensembl_gene_id":"ENSG00000252373.1","gene_symbol":"RNU6-358P","gene_name":"RNA, U6 small nuclear 358, pseudogene [Source:HGNC Symbol;Acc:HGNC:47321]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481291","summary":null,"start":31820564,"end":31820638,"strand":-1,"description":"RNA, U6 small nuclear 358, pseudogene [Source:HGNC Symbol;Acc:HGNC:47321]"}, {"versioned_ensembl_gene_id":"ENSG00000223258.1","gene_symbol":"RNU6-575P","gene_name":"RNA, U6 small nuclear 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:47538]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481363","summary":null,"start":43207762,"end":43207866,"strand":-1,"description":"RNA, U6 small nuclear 575, pseudogene [Source:HGNC Symbol;Acc:HGNC:47538]"}, {"versioned_ensembl_gene_id":"ENSG00000274006.1","gene_symbol":"DLG2-AS1_1","gene_name":"DLG2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02112]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":84887207,"end":84887419,"strand":1,"description":"DLG2 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02112]"}, {"versioned_ensembl_gene_id":"ENSG00000252685.1","gene_symbol":"RNU6-928P","gene_name":"RNA, U6 small nuclear 928, pseudogene [Source:HGNC Symbol;Acc:HGNC:47891]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479977","summary":null,"start":66638271,"end":66638374,"strand":1,"description":"RNA, U6 small nuclear 928, pseudogene [Source:HGNC Symbol;Acc:HGNC:47891]"}, {"versioned_ensembl_gene_id":"ENSG00000252003.1","gene_symbol":"RNU7-154P","gene_name":"RNA, U7 small nuclear 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:45688]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481802","summary":null,"start":122081720,"end":122081781,"strand":1,"description":"RNA, U7 small nuclear 154 pseudogene [Source:HGNC Symbol;Acc:HGNC:45688]"}, {"versioned_ensembl_gene_id":"ENSG00000223109.1","gene_symbol":"MIR1538","gene_name":"microRNA 1538 [Source:HGNC Symbol;Acc:HGNC:35382]","synonyms":"MIRN1538,hsa-mir-1538","biotype":"miRNA","ncbi_id":"100302119","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69565808,"end":69565868,"strand":-1,"description":"microRNA 1538 [Source:HGNC Symbol;Acc:HGNC:35382]"}, {"versioned_ensembl_gene_id":"ENSG00000266417.1","gene_symbol":"MIR4424","gene_name":"microRNA 4424 [Source:HGNC Symbol;Acc:HGNC:41805]","synonyms":"hsa-mir-4424","biotype":"miRNA","ncbi_id":"100616328","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":178677749,"end":178677834,"strand":1,"description":"microRNA 4424 [Source:HGNC Symbol;Acc:HGNC:41805]"}, {"versioned_ensembl_gene_id":"ENSG00000265881.1","gene_symbol":"PDLIM1P2","gene_name":"PDZ and LIM domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48945]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419426","summary":null,"start":21444833,"end":21445439,"strand":-1,"description":"PDZ and LIM domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48945]"}, {"versioned_ensembl_gene_id":"ENSG00000243888.1","gene_symbol":"AL355140.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":69428248,"end":69428721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274314.1","gene_symbol":"MIR6749","gene_name":"microRNA 6749 [Source:HGNC Symbol;Acc:HGNC:50087]","synonyms":"hsa-mir-6749","biotype":"miRNA","ncbi_id":"102466727","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64902387,"end":64902455,"strand":-1,"description":"microRNA 6749 [Source:HGNC Symbol;Acc:HGNC:50087]"}, {"versioned_ensembl_gene_id":"ENSG00000265172.1","gene_symbol":"MIR4262","gene_name":"microRNA 4262 [Source:HGNC Symbol;Acc:HGNC:38308]","synonyms":"hsa-mir-4262","biotype":"miRNA","ncbi_id":"100422996","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11836933,"end":11836986,"strand":-1,"description":"microRNA 4262 [Source:HGNC Symbol;Acc:HGNC:38308]"}, {"versioned_ensembl_gene_id":"ENSG00000211513.5","gene_symbol":"MIR320E","gene_name":"microRNA 320e [Source:HGNC Symbol;Acc:HGNC:38230]","synonyms":"hsa-mir-320e","biotype":"miRNA","ncbi_id":"100422913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46709293,"end":46709345,"strand":-1,"description":"microRNA 320e [Source:HGNC Symbol;Acc:HGNC:38230]"}, {"versioned_ensembl_gene_id":"ENSG00000266081.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32572064,"end":32572207,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000278701.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20340743,"end":20341045,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000251757.1","gene_symbol":"RNU6-848P","gene_name":"RNA, U6 small nuclear 848, pseudogene [Source:HGNC Symbol;Acc:HGNC:47811]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479941","summary":null,"start":130622838,"end":130622944,"strand":1,"description":"RNA, U6 small nuclear 848, pseudogene [Source:HGNC Symbol;Acc:HGNC:47811]"}, {"versioned_ensembl_gene_id":"ENSG00000243059.3","gene_symbol":"RN7SL400P","gene_name":"RNA, 7SL, cytoplasmic 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:46416]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481033","summary":null,"start":21102843,"end":21103138,"strand":-1,"description":"RNA, 7SL, cytoplasmic 400, pseudogene [Source:HGNC Symbol;Acc:HGNC:46416]"}, {"versioned_ensembl_gene_id":"ENSG00000208005.1","gene_symbol":"MIR503","gene_name":"microRNA 503 [Source:HGNC Symbol;Acc:HGNC:32138]","synonyms":"MIRN503,hsa-mir-503","biotype":"miRNA","ncbi_id":"574506","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134546328,"end":134546398,"strand":-1,"description":"microRNA 503 [Source:HGNC Symbol;Acc:HGNC:32138]"}, {"versioned_ensembl_gene_id":"ENSG00000252931.1","gene_symbol":"RNU6-231P","gene_name":"RNA, U6 small nuclear 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:47194]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481251","summary":null,"start":85821855,"end":85821957,"strand":1,"description":"RNA, U6 small nuclear 231, pseudogene [Source:HGNC Symbol;Acc:HGNC:47194]"}, {"versioned_ensembl_gene_id":"ENSG00000238311.1","gene_symbol":"SNORD13E","gene_name":"small nucleolar RNA, C/D box 13E [Source:HGNC Symbol;Acc:HGNC:52254]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617020","summary":null,"start":65696833,"end":65696936,"strand":-1,"description":"small nucleolar RNA, C/D box 13E [Source:HGNC Symbol;Acc:HGNC:52254]"}, {"versioned_ensembl_gene_id":"ENSG00000201610.1","gene_symbol":"RNA5SP84","gene_name":"RNA, 5S ribosomal pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:42882]","synonyms":"RN5S84","biotype":"rRNA","ncbi_id":"100873317","summary":null,"start":11517397,"end":11517503,"strand":1,"description":"RNA, 5S ribosomal pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:42882]"}, {"versioned_ensembl_gene_id":"ENSG00000274072.1","gene_symbol":"mascRNA-menRNA","gene_name":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":65506117,"end":65506173,"strand":1,"description":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]"}, {"versioned_ensembl_gene_id":"ENSG00000201679.1","gene_symbol":"SNORD115-15","gene_name":"small nucleolar RNA, C/D box 115-15 [Source:HGNC Symbol;Acc:HGNC:33034]","synonyms":"HBII-52-15","biotype":"snoRNA","ncbi_id":"100033453","summary":null,"start":25197576,"end":25197656,"strand":1,"description":"small nucleolar RNA, C/D box 115-15 [Source:HGNC Symbol;Acc:HGNC:33034]"}, {"versioned_ensembl_gene_id":"ENSG00000252192.1","gene_symbol":"SNORA9","gene_name":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]","synonyms":"ACA9,SNORA9A","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":122492113,"end":122492241,"strand":-1,"description":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]"}, {"versioned_ensembl_gene_id":"ENSG00000184084.7","gene_symbol":"AC091868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73803296,"end":73803599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256757.1","gene_symbol":"AP002840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113405321,"end":113412117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149295.13","gene_symbol":"DRD2","gene_name":"dopamine receptor D2 [Source:HGNC Symbol;Acc:HGNC:3023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1813","summary":"This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq, Jul 2008]","start":113409615,"end":113475691,"strand":-1,"description":"dopamine receptor D2 [Source:HGNC Symbol;Acc:HGNC:3023]"}, {"versioned_ensembl_gene_id":"ENSG00000242888.1","gene_symbol":"AL133368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99974336,"end":99975149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264060.1","gene_symbol":"MIR4316","gene_name":"microRNA 4316 [Source:HGNC Symbol;Acc:HGNC:38306]","synonyms":"hsa-mir-4316","biotype":"miRNA","ncbi_id":"100422851","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77396984,"end":77397054,"strand":-1,"description":"microRNA 4316 [Source:HGNC Symbol;Acc:HGNC:38306]"}, {"versioned_ensembl_gene_id":"ENSG00000264566.3","gene_symbol":"MIR23C","gene_name":"microRNA 23c [Source:HGNC Symbol;Acc:HGNC:38913]","synonyms":"hsa-mir-23c","biotype":"miRNA","ncbi_id":"100500809","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20017088,"end":20017187,"strand":-1,"description":"microRNA 23c [Source:HGNC Symbol;Acc:HGNC:38913]"}, {"versioned_ensembl_gene_id":"ENSG00000199133.3","gene_symbol":"MIRLET7D","gene_name":"microRNA let-7d [Source:HGNC Symbol;Acc:HGNC:31481]","synonyms":"MIRNLET7D,hsa-let-7d","biotype":"miRNA","ncbi_id":"406886","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94178834,"end":94178920,"strand":1,"description":"microRNA let-7d [Source:HGNC Symbol;Acc:HGNC:31481]"}, {"versioned_ensembl_gene_id":"ENSG00000200377.1","gene_symbol":"SNORD56","gene_name":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]","synonyms":"U56,RNU56","biotype":"snoRNA","ncbi_id":"26793","summary":null,"start":153446813,"end":153446883,"strand":-1,"description":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]"}, {"versioned_ensembl_gene_id":"ENSG00000283609.1","gene_symbol":"MIR4662A","gene_name":"microRNA 4662a [Source:HGNC Symbol;Acc:HGNC:41826]","synonyms":"hsa-mir-4662a","biotype":"miRNA","ncbi_id":"100616221","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124821985,"end":124822051,"strand":1,"description":"microRNA 4662a [Source:HGNC Symbol;Acc:HGNC:41826]"}, {"versioned_ensembl_gene_id":"ENSG00000253047.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":150600539,"end":150600659,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000199360.1","gene_symbol":"RNU6-1115P","gene_name":"RNA, U6 small nuclear 1115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48078]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480639","summary":null,"start":110856417,"end":110856522,"strand":1,"description":"RNA, U6 small nuclear 1115, pseudogene [Source:HGNC Symbol;Acc:HGNC:48078]"}, {"versioned_ensembl_gene_id":"ENSG00000265278.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31653519,"end":31653632,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207053.1","gene_symbol":"RNU6-937P","gene_name":"RNA, U6 small nuclear 937, pseudogene [Source:HGNC Symbol;Acc:HGNC:47900]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479980","summary":null,"start":35928570,"end":35928675,"strand":-1,"description":"RNA, U6 small nuclear 937, pseudogene [Source:HGNC Symbol;Acc:HGNC:47900]"}, {"versioned_ensembl_gene_id":"ENSG00000223131.1","gene_symbol":"RNA5SP304","gene_name":"RNA, 5S ribosomal pseudogene 304 [Source:HGNC Symbol;Acc:HGNC:43204]","synonyms":"RN5S304","biotype":"rRNA","ncbi_id":"100873578","summary":null,"start":22997255,"end":22997358,"strand":1,"description":"RNA, 5S ribosomal pseudogene 304 [Source:HGNC Symbol;Acc:HGNC:43204]"}, {"versioned_ensembl_gene_id":"ENSG00000252157.1","gene_symbol":"RNU6-479P","gene_name":"RNA, U6 small nuclear 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:47442]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481331","summary":null,"start":183653572,"end":183653676,"strand":-1,"description":"RNA, U6 small nuclear 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:47442]"}, {"versioned_ensembl_gene_id":"ENSG00000201954.1","gene_symbol":"RNU6-673P","gene_name":"RNA, U6 small nuclear 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:47636]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481394","summary":null,"start":76260800,"end":76260903,"strand":-1,"description":"RNA, U6 small nuclear 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:47636]"}, {"versioned_ensembl_gene_id":"ENSG00000222413.1","gene_symbol":"RN7SKP125","gene_name":"RNA, 7SK small nuclear pseudogene 125 [Source:HGNC Symbol;Acc:HGNC:45849]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479150","summary":null,"start":117276985,"end":117277286,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 125 [Source:HGNC Symbol;Acc:HGNC:45849]"}, {"versioned_ensembl_gene_id":"ENSG00000252759.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":200863152,"end":200863247,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276275.1","gene_symbol":"SNORD5","gene_name":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]","synonyms":"mgh28S-2410","biotype":"snoRNA","ncbi_id":"692072","summary":null,"start":141453377,"end":141453451,"strand":1,"description":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]"}, {"versioned_ensembl_gene_id":"ENSG00000168350.7","gene_symbol":"DEGS2","gene_name":"delta 4-desaturase, sphingolipid 2 [Source:HGNC Symbol;Acc:HGNC:20113]","synonyms":"FADS8,DES2,C14orf66","biotype":"protein_coding","ncbi_id":"123099","summary":"This gene encodes a bifunctional enzyme that is involved in the biosynthesis of phytosphingolipids in human skin and in other phytosphingolipid-containing tissues. This enzyme can act as a sphingolipid delta(4)-desaturase, and also as a sphingolipid C4-hydroxylase. [provided by RefSeq, Oct 2008]","start":100143957,"end":100160163,"strand":-1,"description":"delta 4-desaturase, sphingolipid 2 [Source:HGNC Symbol;Acc:HGNC:20113]"}, {"versioned_ensembl_gene_id":"ENSG00000272071.1","gene_symbol":"AC122710.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6779458,"end":6779998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185269.11","gene_symbol":"NOTUM","gene_name":"NOTUM, palmitoleoyl-protein carboxylesterase [Source:HGNC Symbol;Acc:HGNC:27106]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147111","summary":null,"start":81952507,"end":81961840,"strand":-1,"description":"NOTUM, palmitoleoyl-protein carboxylesterase [Source:HGNC Symbol;Acc:HGNC:27106]"}, {"versioned_ensembl_gene_id":"ENSG00000284149.1","gene_symbol":"MIR4784","gene_name":"microRNA 4784 [Source:HGNC Symbol;Acc:HGNC:41580]","synonyms":"hsa-mir-4784","biotype":"miRNA","ncbi_id":"100616378","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":131491160,"end":131491236,"strand":-1,"description":"microRNA 4784 [Source:HGNC Symbol;Acc:HGNC:41580]"}, {"versioned_ensembl_gene_id":"ENSG00000264864.1","gene_symbol":"MIR3613","gene_name":"microRNA 3613 [Source:HGNC Symbol;Acc:HGNC:38964]","synonyms":"hsa-mir-3613","biotype":"miRNA","ncbi_id":"100500908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49996415,"end":49996501,"strand":-1,"description":"microRNA 3613 [Source:HGNC Symbol;Acc:HGNC:38964]"}, {"versioned_ensembl_gene_id":"ENSG00000238302.1","gene_symbol":"RNU7-120P","gene_name":"RNA, U7 small nuclear 120 pseudogene [Source:HGNC Symbol;Acc:HGNC:45654]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480817","summary":null,"start":89282223,"end":89282285,"strand":-1,"description":"RNA, U7 small nuclear 120 pseudogene [Source:HGNC Symbol;Acc:HGNC:45654]"}, {"versioned_ensembl_gene_id":"ENSG00000272025.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":65158662,"end":65158860,"strand":1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000200325.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30309015,"end":30309126,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241291.3","gene_symbol":"RN7SL791P","gene_name":"RNA, 7SL, cytoplasmic 791, pseudogene [Source:HGNC Symbol;Acc:HGNC:46807]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481860","summary":null,"start":146656401,"end":146656695,"strand":-1,"description":"RNA, 7SL, cytoplasmic 791, pseudogene [Source:HGNC Symbol;Acc:HGNC:46807]"}, {"versioned_ensembl_gene_id":"ENSG00000206878.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":228652436,"end":228652560,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000206680.1","gene_symbol":"SNORD21","gene_name":"small nucleolar RNA, C/D box 21 [Source:HGNC Symbol;Acc:HGNC:10144]","synonyms":"U21,RNU21","biotype":"snoRNA","ncbi_id":"6083","summary":"This gene encodes a small nucleolar RNA (snoRNA) that may be involved in biogenesis of the large (28S) ribosomal subunit. This gene is found within an intron of the RPL5 gene. [provided by RefSeq, Mar 2009]","start":92837289,"end":92837383,"strand":1,"description":"small nucleolar RNA, C/D box 21 [Source:HGNC Symbol;Acc:HGNC:10144]"}, {"versioned_ensembl_gene_id":"ENSG00000207600.3","gene_symbol":"MIR598","gene_name":"microRNA 598 [Source:HGNC Symbol;Acc:HGNC:32854]","synonyms":"MIRN598,hsa-mir-598","biotype":"miRNA","ncbi_id":"693183","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11035206,"end":11035302,"strand":-1,"description":"microRNA 598 [Source:HGNC Symbol;Acc:HGNC:32854]"}, {"versioned_ensembl_gene_id":"ENSG00000266618.1","gene_symbol":"MIR4742","gene_name":"microRNA 4742 [Source:HGNC Symbol;Acc:HGNC:41565]","synonyms":"hsa-mir-4742","biotype":"miRNA","ncbi_id":"100616468","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":224398227,"end":224398311,"strand":-1,"description":"microRNA 4742 [Source:HGNC Symbol;Acc:HGNC:41565]"}, {"versioned_ensembl_gene_id":"ENSG00000263511.1","gene_symbol":"MIR5699","gene_name":"microRNA 5699 [Source:HGNC Symbol;Acc:HGNC:43456]","synonyms":"hsa-mir-5699","biotype":"miRNA","ncbi_id":"100847086","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":641689,"end":641778,"strand":-1,"description":"microRNA 5699 [Source:HGNC Symbol;Acc:HGNC:43456]"}, {"versioned_ensembl_gene_id":"ENSG00000185105.5","gene_symbol":"MYADML2","gene_name":"myeloid associated differentiation marker like 2 [Source:HGNC Symbol;Acc:HGNC:34548]","synonyms":"LOC255275","biotype":"protein_coding","ncbi_id":"255275","summary":null,"start":81939645,"end":81947233,"strand":-1,"description":"myeloid associated differentiation marker like 2 [Source:HGNC Symbol;Acc:HGNC:34548]"}, {"versioned_ensembl_gene_id":"ENSG00000167842.15","gene_symbol":"MIS12","gene_name":"MIS12, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24967]","synonyms":"MTW1,MGC2488,KNTC2AP,hMIS12","biotype":"protein_coding","ncbi_id":"79003","summary":null,"start":5486285,"end":5490814,"strand":1,"description":"MIS12, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24967]"}, {"versioned_ensembl_gene_id":"ENSG00000275091.1","gene_symbol":"AC022098.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14006422,"end":14006773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277817.1","gene_symbol":"MIR6738","gene_name":"microRNA 6738 [Source:HGNC Symbol;Acc:HGNC:49939]","synonyms":"hsa-mir-6738","biotype":"miRNA","ncbi_id":"102465442","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155951273,"end":155951336,"strand":-1,"description":"microRNA 6738 [Source:HGNC Symbol;Acc:HGNC:49939]"}, {"versioned_ensembl_gene_id":"ENSG00000266144.1","gene_symbol":"MIR4654","gene_name":"microRNA 4654 [Source:HGNC Symbol;Acc:HGNC:41643]","synonyms":"hsa-mir-4654","biotype":"miRNA","ncbi_id":"100616386","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":162157107,"end":162157182,"strand":1,"description":"microRNA 4654 [Source:HGNC Symbol;Acc:HGNC:41643]"}, {"versioned_ensembl_gene_id":"ENSG00000284247.1","gene_symbol":"MIR2682","gene_name":"microRNA 2682 [Source:HGNC Symbol;Acc:HGNC:41688]","synonyms":"hsa-mir-2682","biotype":"miRNA","ncbi_id":"100616452","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98045242,"end":98045351,"strand":-1,"description":"microRNA 2682 [Source:HGNC Symbol;Acc:HGNC:41688]"}, {"versioned_ensembl_gene_id":"ENSG00000266110.1","gene_symbol":"MIR4423","gene_name":"microRNA 4423 [Source:HGNC Symbol;Acc:HGNC:41784]","synonyms":"hsa-mir-4423","biotype":"miRNA","ncbi_id":"100616481","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85133794,"end":85133873,"strand":1,"description":"microRNA 4423 [Source:HGNC Symbol;Acc:HGNC:41784]"}, {"versioned_ensembl_gene_id":"ENSG00000222370.1","gene_symbol":"SNORA36B","gene_name":"small nucleolar RNA, H/ACA box 36B [Source:HGNC Symbol;Acc:HGNC:32629]","synonyms":"ACA36b","biotype":"snoRNA","ncbi_id":"677818","summary":null,"start":220200546,"end":220200676,"strand":-1,"description":"small nucleolar RNA, H/ACA box 36B [Source:HGNC Symbol;Acc:HGNC:32629]"}, {"versioned_ensembl_gene_id":"ENSG00000251728.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140094697,"end":140094792,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206603.1","gene_symbol":"SNORA22B","gene_name":"small nucleolar RNA, H/ACA box 22B [Source:HGNC Symbol;Acc:HGNC:52196]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616964","summary":null,"start":56055365,"end":56055502,"strand":1,"description":"small nucleolar RNA, H/ACA box 22B [Source:HGNC Symbol;Acc:HGNC:52196]"}, {"versioned_ensembl_gene_id":"ENSG00000265421.1","gene_symbol":"MIR4459","gene_name":"microRNA 4459 [Source:HGNC Symbol;Acc:HGNC:41551]","synonyms":"hsa-mir-4459","biotype":"miRNA","ncbi_id":"100616233","summary":"This record was withdrawn by miRBase.","start":54075518,"end":54075583,"strand":-1,"description":"microRNA 4459 [Source:HGNC Symbol;Acc:HGNC:41551]"}, {"versioned_ensembl_gene_id":"ENSG00000273839.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28500089,"end":28500346,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252108.1","gene_symbol":"RNU6-1232P","gene_name":"RNA, U6 small nuclear 1232, pseudogene [Source:HGNC Symbol;Acc:HGNC:48195]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480105","summary":null,"start":68159061,"end":68159146,"strand":-1,"description":"RNA, U6 small nuclear 1232, pseudogene [Source:HGNC Symbol;Acc:HGNC:48195]"}, {"versioned_ensembl_gene_id":"ENSG00000275304.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54539846,"end":54539952,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283950.1","gene_symbol":"MIR6791","gene_name":"microRNA 6791 [Source:HGNC Symbol;Acc:HGNC:50097]","synonyms":"hsa-mir-6791","biotype":"miRNA","ncbi_id":"102465474","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6736712,"end":6736778,"strand":-1,"description":"microRNA 6791 [Source:HGNC Symbol;Acc:HGNC:50097]"}, {"versioned_ensembl_gene_id":"ENSG00000072849.10","gene_symbol":"DERL2","gene_name":"derlin 2 [Source:HGNC Symbol;Acc:HGNC:17943]","synonyms":"FLANa,F-LANa,F-LAN-1,derlin-2,CGI-101","biotype":"protein_coding","ncbi_id":"51009","summary":"Proteins that are unfolded or misfolded in the endoplasmic reticulum (ER) must be refolded or degraded to maintain the homeostasis of the ER. DERL2 is involved in the degradation of misfolded glycoproteins in the ER (Oda et al., 2006 [PubMed 16449189]).[supplied by OMIM, Mar 2008]","start":5471251,"end":5486811,"strand":-1,"description":"derlin 2 [Source:HGNC Symbol;Acc:HGNC:17943]"}, {"versioned_ensembl_gene_id":"ENSG00000202146.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":54099191,"end":54099302,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277533.1","gene_symbol":"MIR8077","gene_name":"microRNA 8077 [Source:HGNC Symbol;Acc:HGNC:50266]","synonyms":"hsa-mir-8077","biotype":"miRNA","ncbi_id":"102465875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42351131,"end":42351205,"strand":1,"description":"microRNA 8077 [Source:HGNC Symbol;Acc:HGNC:50266]"}, {"versioned_ensembl_gene_id":"ENSG00000264468.1","gene_symbol":"MIR4520-1","gene_name":"microRNA 4520-1 [Source:HGNC Symbol;Acc:HGNC:41775]","synonyms":"MIR4520A,hsa-mir-4520a","biotype":"miRNA","ncbi_id":"100616401","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6655440,"end":6655509,"strand":-1,"description":"microRNA 4520-1 [Source:HGNC Symbol;Acc:HGNC:41775]"}, {"versioned_ensembl_gene_id":"ENSG00000208001.1","gene_symbol":"MIR431","gene_name":"microRNA 431 [Source:HGNC Symbol;Acc:HGNC:32027]","synonyms":"MIRN431,hsa-mir-431","biotype":"miRNA","ncbi_id":"574038","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100881007,"end":100881120,"strand":1,"description":"microRNA 431 [Source:HGNC Symbol;Acc:HGNC:32027]"}, {"versioned_ensembl_gene_id":"ENSG00000263643.1","gene_symbol":"MIR4515","gene_name":"microRNA 4515 [Source:HGNC Symbol;Acc:HGNC:41800]","synonyms":"hsa-mir-4515","biotype":"miRNA","ncbi_id":"100616404","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":83067335,"end":83067415,"strand":1,"description":"microRNA 4515 [Source:HGNC Symbol;Acc:HGNC:41800]"}, {"versioned_ensembl_gene_id":"ENSG00000276873.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39171462,"end":39171560,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000278038.1","gene_symbol":"MIR6076","gene_name":"microRNA 6076 [Source:HGNC Symbol;Acc:HGNC:50232]","synonyms":"hsa-mir-6076","biotype":"miRNA","ncbi_id":"102464828","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49966399,"end":49966511,"strand":1,"description":"microRNA 6076 [Source:HGNC Symbol;Acc:HGNC:50232]"}, {"versioned_ensembl_gene_id":"ENSG00000265793.1","gene_symbol":"MIR3118-4","gene_name":"microRNA 3118-4 [Source:HGNC Symbol;Acc:HGNC:38287]","synonyms":"hsa-mir-3118-4","biotype":"miRNA","ncbi_id":"100422935","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21843750,"end":21843824,"strand":1,"description":"microRNA 3118-4 [Source:HGNC Symbol;Acc:HGNC:38287]"}, {"versioned_ensembl_gene_id":"ENSG00000171136.6","gene_symbol":"RLN3","gene_name":"relaxin 3 [Source:HGNC Symbol;Acc:HGNC:17135]","synonyms":"ZINS4,RXN3,H3","biotype":"protein_coding","ncbi_id":"117579","summary":"This gene encodes a member of the relaxin family of insulin-like hormones that is expressed predominantly in the brain and plays a role in physiological processes such as stress, memory and appetite regulation. The encoded protein is a precursor that is proteolytically processed to generate a heterodimeric mature form consisting A and B chains interlinked by disulfide bonds. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2015]","start":14028148,"end":14031042,"strand":1,"description":"relaxin 3 [Source:HGNC Symbol;Acc:HGNC:17135]"}, {"versioned_ensembl_gene_id":"ENSG00000284115.1","gene_symbol":"AC113189.10","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7439506,"end":7445966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266174.1","gene_symbol":"MIR4666A","gene_name":"microRNA 4666a [Source:HGNC Symbol;Acc:HGNC:41750]","synonyms":"MIR4666,hsa-mir-4666","biotype":"miRNA","ncbi_id":"100616308","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":228462074,"end":228462152,"strand":1,"description":"microRNA 4666a [Source:HGNC Symbol;Acc:HGNC:41750]"}, {"versioned_ensembl_gene_id":"ENSG00000275635.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":23137805,"end":23137864,"strand":-1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000243103.3","gene_symbol":"RN7SL452P","gene_name":"RNA, 7SL, cytoplasmic 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:46468]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479387","summary":null,"start":50637691,"end":50637981,"strand":-1,"description":"RNA, 7SL, cytoplasmic 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:46468]"}, {"versioned_ensembl_gene_id":"ENSG00000212546.1","gene_symbol":"RNU6-995P","gene_name":"RNA, U6 small nuclear 995, pseudogene [Source:HGNC Symbol;Acc:HGNC:47958]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481494","summary":null,"start":80936434,"end":80936540,"strand":1,"description":"RNA, U6 small nuclear 995, pseudogene [Source:HGNC Symbol;Acc:HGNC:47958]"}, {"versioned_ensembl_gene_id":"ENSG00000201413.1","gene_symbol":"RNA5SP141","gene_name":"RNA, 5S ribosomal pseudogene 141 [Source:HGNC Symbol;Acc:HGNC:43041]","synonyms":"RN5S141","biotype":"rRNA","ncbi_id":"100873408","summary":null,"start":134783436,"end":134783555,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 141 [Source:HGNC Symbol;Acc:HGNC:43041]"}, {"versioned_ensembl_gene_id":"ENSG00000242236.2","gene_symbol":"RN7SL594P","gene_name":"RNA, 7SL, cytoplasmic 594, pseudogene [Source:HGNC Symbol;Acc:HGNC:46610]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479439","summary":null,"start":25654595,"end":25654881,"strand":-1,"description":"RNA, 7SL, cytoplasmic 594, pseudogene [Source:HGNC Symbol;Acc:HGNC:46610]"}, {"versioned_ensembl_gene_id":"ENSG00000207416.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36986739,"end":36986851,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284363.1","gene_symbol":"MIR224","gene_name":"microRNA 224 [Source:HGNC Symbol;Acc:HGNC:31604]","synonyms":"MIRN224,hsa-mir-224","biotype":"miRNA","ncbi_id":"407009","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151958578,"end":151958658,"strand":-1,"description":"microRNA 224 [Source:HGNC Symbol;Acc:HGNC:31604]"}, {"versioned_ensembl_gene_id":"ENSG00000278527.1","gene_symbol":"SNORD22","gene_name":"Small nucleolar RNA SNORD22 [Source:RFAM;Acc:RF00099]","synonyms":"RNU22,U22","biotype":"snoRNA","ncbi_id":"9304","summary":null,"start":62854161,"end":62854285,"strand":-1,"description":"Small nucleolar RNA SNORD22 [Source:RFAM;Acc:RF00099]"}, {"versioned_ensembl_gene_id":"ENSG00000284157.1","gene_symbol":"MIR106A","gene_name":"microRNA 106a [Source:HGNC Symbol;Acc:HGNC:31494]","synonyms":"MIRN106A,hsa-mir-106a","biotype":"miRNA","ncbi_id":"406899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134170198,"end":134170278,"strand":-1,"description":"microRNA 106a [Source:HGNC Symbol;Acc:HGNC:31494]"}, {"versioned_ensembl_gene_id":"ENSG00000275335.1","gene_symbol":"MIR8088","gene_name":"microRNA 8088 [Source:HGNC Symbol;Acc:HGNC:50167]","synonyms":"hsa-mir-8088","biotype":"miRNA","ncbi_id":"102466880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52336557,"end":52336642,"strand":-1,"description":"microRNA 8088 [Source:HGNC Symbol;Acc:HGNC:50167]"}, {"versioned_ensembl_gene_id":"ENSG00000207587.1","gene_symbol":"MIR544A","gene_name":"microRNA 544a [Source:HGNC Symbol;Acc:HGNC:32530]","synonyms":"MIRN544,MIR544,hsa-mir-544","biotype":"miRNA","ncbi_id":"664613","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101048658,"end":101048748,"strand":1,"description":"microRNA 544a [Source:HGNC Symbol;Acc:HGNC:32530]"}, {"versioned_ensembl_gene_id":"ENSG00000276421.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"PRP31,hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000266016.3","gene_symbol":"MIR548Z","gene_name":"microRNA 548z [Source:HGNC Symbol;Acc:HGNC:38929]","synonyms":"hsa-mir-548z","biotype":"miRNA","ncbi_id":"100500856","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64622509,"end":64622605,"strand":-1,"description":"microRNA 548z [Source:HGNC Symbol;Acc:HGNC:38929]"}, {"versioned_ensembl_gene_id":"ENSG00000279724.1","gene_symbol":"AC005086.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":102188599,"end":102188828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146250.6","gene_symbol":"PRSS35","gene_name":"protease, serine 35 [Source:HGNC Symbol;Acc:HGNC:21387]","synonyms":"MGC46520,dJ223E3.1,C6orf158","biotype":"protein_coding","ncbi_id":"167681","summary":null,"start":83512538,"end":83525704,"strand":1,"description":"protease, serine 35 [Source:HGNC Symbol;Acc:HGNC:21387]"}, {"versioned_ensembl_gene_id":"ENSG00000173156.6","gene_symbol":"RHOD","gene_name":"ras homolog family member D [Source:HGNC Symbol;Acc:HGNC:670]","synonyms":"RhoHP1,RhoD,Rho,ARHD","biotype":"protein_coding","ncbi_id":"29984","summary":"Ras homolog, or Rho, proteins interact with protein kinases and may serve as targets for activated GTPase. They play a critical role in muscle differentiation. The protein encoded by this gene binds GTP and is a member of the small GTPase superfamily. It is involved in endosome dynamics and reorganization of the actin cytoskeleton, and it may coordinate membrane transport with the function of the cytoskeleton. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":67056818,"end":67072013,"strand":1,"description":"ras homolog family member D [Source:HGNC Symbol;Acc:HGNC:670]"}, {"versioned_ensembl_gene_id":"ENSG00000124279.11","gene_symbol":"FASTKD3","gene_name":"FAST kinase domains 3 [Source:HGNC Symbol;Acc:HGNC:28758]","synonyms":"MGC5297,FLJ23274","biotype":"protein_coding","ncbi_id":"79072","summary":"This gene encodes a member of a small family of Fas-activated serine/threonine kinase domain (FASTKD) containing proteins that share an amino terminal mitochondrial targeting domain and multiple carboxy terminal FAST domains as well as a putative RNA-binding RAP domain. The members of this family are ubiquitously expressed and are generally most abundant in mitochondria-enriched tissues such as heart, skeletal muscle and brown-adipose tissue. Some members of this protein family may play a role in apoptosis. The protein encoded by this gene interacts with components of the mitochondrial respiratory and translation networks. A pseudogene of this gene is also present on chromosome 5. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":7859159,"end":7869037,"strand":-1,"description":"FAST kinase domains 3 [Source:HGNC Symbol;Acc:HGNC:28758]"}, {"versioned_ensembl_gene_id":"ENSG00000223783.1","gene_symbol":"LINC01983","gene_name":"long intergenic non-protein coding RNA 1983 [Source:HGNC Symbol;Acc:HGNC:52813]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929697","summary":null,"start":195836193,"end":195860404,"strand":-1,"description":"long intergenic non-protein coding RNA 1983 [Source:HGNC Symbol;Acc:HGNC:52813]"}, {"versioned_ensembl_gene_id":"ENSG00000124275.14","gene_symbol":"MTRR","gene_name":"5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Source:HGNC Symbol;Acc:HGNC:7473]","synonyms":"cblE","biotype":"protein_coding","ncbi_id":"4552","summary":"This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":7851186,"end":7906025,"strand":1,"description":"5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Source:HGNC Symbol;Acc:HGNC:7473]"}, {"versioned_ensembl_gene_id":"ENSG00000282980.1","gene_symbol":"AC055839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5512040,"end":5512537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091592.15","gene_symbol":"NLRP1","gene_name":"NLR family pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14374]","synonyms":"NALP1,NAC,KIAA0926,DKFZp586O1822,DEFCAP,CLR17.1,CARD7,VAMAS1,SLEV1","biotype":"protein_coding","ncbi_id":"22861","summary":"This gene encodes a member of the Ced-4 family of apoptosis proteins. Ced-family members contain a caspase recruitment domain (CARD) and are known to be key mediators of programmed cell death. The encoded protein contains a distinct N-terminal pyrin-like motif, which is possibly involved in protein-protein interactions. This protein interacts strongly with caspase 2 and weakly with caspase 9. Overexpression of this gene was demonstrated to induce apoptosis in cells. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":5499427,"end":5619424,"strand":-1,"description":"NLR family pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14374]"}, {"versioned_ensembl_gene_id":"ENSG00000198625.12","gene_symbol":"MDM4","gene_name":"MDM4, p53 regulator [Source:HGNC Symbol;Acc:HGNC:6974]","synonyms":"MDMX,HDMX","biotype":"protein_coding","ncbi_id":"4194","summary":"This gene encodes a nuclear protein that contains a p53 binding domain at the N-terminus and a RING finger domain at the C-terminus, and shows structural similarity to p53-binding protein MDM2. Both proteins bind the p53 tumor suppressor protein and inhibit its activity, and have been shown to be overexpressed in a variety of human cancers. However, unlike MDM2 which degrades p53, this protein inhibits p53 by binding its transcriptional activation domain. This protein also interacts with MDM2 protein via the RING finger domain, and inhibits the latter's degradation. So this protein can reverse MDM2-targeted degradation of p53, while maintaining suppression of p53 transactivation and apoptotic functions. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2011]","start":204516379,"end":204558120,"strand":1,"description":"MDM4, p53 regulator [Source:HGNC Symbol;Acc:HGNC:6974]"}, {"versioned_ensembl_gene_id":"ENSG00000264811.1","gene_symbol":"AC138761.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22299134,"end":22299467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257101.1","gene_symbol":"LRRC37A13P","gene_name":"leucine rich repeat containing 37 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:43817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479024","summary":null,"start":113791466,"end":113791752,"strand":1,"description":"leucine rich repeat containing 37 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:43817]"}, {"versioned_ensembl_gene_id":"ENSG00000126457.21","gene_symbol":"PRMT1","gene_name":"protein arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5187]","synonyms":"HRMT1L2,HCP1,ANM1","biotype":"protein_coding","ncbi_id":"3276","summary":"This gene encodes a member of the protein arginine N-methyltransferase (PRMT) family. Post-translational modification of target proteins by PRMTs plays an important regulatory role in many biological processes, whereby PRMTs methylate arginine residues by transferring methyl groups from S-adenosyl-L-methionine to terminal guanidino nitrogen atoms. The encoded protein is a type I PRMT and is responsible for the majority of cellular arginine methylation activity. Increased expression of this gene may play a role in many types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2011]","start":49675786,"end":49689029,"strand":1,"description":"protein arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5187]"}, {"versioned_ensembl_gene_id":"ENSG00000265043.1","gene_symbol":"AC068418.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21456513,"end":21460215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183010.16","gene_symbol":"PYCR1","gene_name":"pyrroline-5-carboxylate reductase 1 [Source:HGNC Symbol;Acc:HGNC:9721]","synonyms":"P5C","biotype":"protein_coding","ncbi_id":"5831","summary":"This gene encodes an enzyme that catalyzes the NAD(P)H-dependent conversion of pyrroline-5-carboxylate to proline. This enzyme may also play a physiologic role in the generation of NADP(+) in some cell types. The protein forms a homopolymer and localizes to the mitochondrion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":81932384,"end":81942412,"strand":-1,"description":"pyrroline-5-carboxylate reductase 1 [Source:HGNC Symbol;Acc:HGNC:9721]"}, {"versioned_ensembl_gene_id":"ENSG00000197063.10","gene_symbol":"MAFG","gene_name":"MAF bZIP transcription factor G [Source:HGNC Symbol;Acc:HGNC:6781]","synonyms":"MGC20149,MGC13090","biotype":"protein_coding","ncbi_id":"4097","summary":"Globin gene expression is regulated through nuclear factor erythroid-2 (NFE2) elements located in enhancer-like locus control regions positioned many kb upstream of alpha- and beta-gene clusters (summarized by Blank et al., 1997 [PubMed 9166829]). NFE2 DNA-binding activity consists of a heterodimer containing a ubiquitous small Maf protein (MafF, MIM 604877; MafG; or MafK, MIM 600197) and the tissue-restricted protein p45 NFE2 (MIM 601490). Both subunits are members of the activator protein-1-like superfamily of basic leucine zipper (bZIP) proteins (see MIM 165160).[supplied by OMIM, Mar 2010]","start":81918270,"end":81927714,"strand":-1,"description":"MAF bZIP transcription factor G [Source:HGNC Symbol;Acc:HGNC:6781]"}, {"versioned_ensembl_gene_id":"ENSG00000004939.13","gene_symbol":"SLC4A1","gene_name":"solute carrier family 4 member 1 (Diego blood group) [Source:HGNC Symbol;Acc:HGNC:11027]","synonyms":"FR,EPB3,DI,CD233,AE1,WR,WD,SW,RTA1A","biotype":"protein_coding","ncbi_id":"6521","summary":"The protein encoded by this gene is part of the anion exchanger (AE) family and is expressed in the erythrocyte plasma membrane, where it functions as a chloride/bicarbonate exchanger involved in carbon dioxide transport from tissues to lungs. The protein comprises two domains that are structurally and functionally distinct. The N-terminal 40kDa domain is located in the cytoplasm and acts as an attachment site for the red cell skeleton by binding ankyrin. The glycosylated C-terminal membrane-associated domain contains 12-14 membrane spanning segments and carries out the stilbene disulphonate-sensitive exchange transport of anions. The cytoplasmic tail at the extreme C-terminus of the membrane domain binds carbonic anhydrase II. The encoded protein associates with the red cell membrane protein glycophorin A and this association promotes the correct folding and translocation of the exchanger. This protein is predominantly dimeric but forms tetramers in the presence of ankyrin. Many mutations in this gene are known in man, and these mutations can lead to two types of disease: destabilization of red cell membrane leading to hereditary spherocytosis, and defective kidney acid secretion leading to distal renal tubular acidosis. Other mutations that do not give rise to disease result in novel blood group antigens, which form the Diego blood group system. Southeast Asian ovalocytosis (SAO, Melanesian ovalocytosis) results from the heterozygous presence of a deletion in the encoded protein and is common in areas where Plasmodium falciparum malaria is endemic. One null mutation in this gene is known, resulting in very severe anemia and nephrocalcinosis. [provided by RefSeq, Jul 2008]","start":44248385,"end":44268141,"strand":-1,"description":"solute carrier family 4 member 1 (Diego blood group) [Source:HGNC Symbol;Acc:HGNC:11027]"}, {"versioned_ensembl_gene_id":"ENSG00000267691.1","gene_symbol":"AC003102.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44228760,"end":44230228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258400.1","gene_symbol":"AL591767.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49707667,"end":49708792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197776.7","gene_symbol":"KLHDC1","gene_name":"kelch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19836]","synonyms":"MST025","biotype":"protein_coding","ncbi_id":"122773","summary":null,"start":49693105,"end":49753152,"strand":1,"description":"kelch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19836]"}, {"versioned_ensembl_gene_id":"ENSG00000104870.12","gene_symbol":"FCGRT","gene_name":"Fc fragment of IgG receptor and transporter [Source:HGNC Symbol;Acc:HGNC:3621]","synonyms":"alpha-chain,FCRN","biotype":"protein_coding","ncbi_id":"2217","summary":"This gene encodes a receptor that binds the Fc region of monomeric immunoglobulin G. The encoded protein transfers immunoglobulin G antibodies from mother to fetus across the placenta. This protein also binds immunoglobulin G to protect the antibody from degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":49506816,"end":49526333,"strand":1,"description":"Fc fragment of IgG receptor and transporter [Source:HGNC Symbol;Acc:HGNC:3621]"}, {"versioned_ensembl_gene_id":"ENSG00000224797.1","gene_symbol":"AL359092.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130724786,"end":130725050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249605.1","gene_symbol":"AC008652.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":144369334,"end":144385310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266074.8","gene_symbol":"BAHCC1","gene_name":"BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29279]","synonyms":"KIAA1447,BAHD2","biotype":"protein_coding","ncbi_id":"57597","summary":null,"start":81395475,"end":81466332,"strand":1,"description":"BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29279]"}, {"versioned_ensembl_gene_id":"ENSG00000274833.1","gene_symbol":"AC110285.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81387415,"end":81387766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258462.2","gene_symbol":"AL591767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49681302,"end":49681886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249637.1","gene_symbol":"AC008438.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140370891,"end":140401367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113580.14","gene_symbol":"NR3C1","gene_name":"nuclear receptor subfamily 3 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7978]","synonyms":"GRL,GR","biotype":"protein_coding","ncbi_id":"2908","summary":"This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors. This receptor is typically found in the cytoplasm, but upon ligand binding, is transported into the nucleus. It is involved in inflammatory responses, cellular proliferation, and differentiation in target tissues. Mutations in this gene are associated with generalized glucocorticoid resistance. Alternative splicing of this gene results in transcript variants encoding either the same or different isoforms. Additional isoforms resulting from the use of alternate in-frame translation initiation sites have also been described, and shown to be functional, displaying diverse cytoplasm-to-nucleus trafficking patterns and distinct transcriptional activities (PMID:15866175). [provided by RefSeq, Feb 2011]","start":143277931,"end":143435512,"strand":-1,"description":"nuclear receptor subfamily 3 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7978]"}, {"versioned_ensembl_gene_id":"ENSG00000148357.16","gene_symbol":"HMCN2","gene_name":"hemicentin 2 [Source:HGNC Symbol;Acc:HGNC:21293]","synonyms":"FLJ23816,DKFZp434P0216","biotype":"protein_coding","ncbi_id":"256158","summary":null,"start":130265882,"end":130434123,"strand":1,"description":"hemicentin 2 [Source:HGNC Symbol;Acc:HGNC:21293]"}, {"versioned_ensembl_gene_id":"ENSG00000131023.12","gene_symbol":"LATS1","gene_name":"large tumor suppressor kinase 1 [Source:HGNC Symbol;Acc:HGNC:6514]","synonyms":"WARTS","biotype":"protein_coding","ncbi_id":"9113","summary":"The protein encoded by this gene is a putative serine/threonine kinase that localizes to the mitotic apparatus and complexes with cell cycle controller CDC2 kinase in early mitosis. The protein is phosphorylated in a cell-cycle dependent manner, with late prophase phosphorylation remaining through metaphase. The N-terminal region of the protein binds CDC2 to form a complex showing reduced H1 histone kinase activity, indicating a role as a negative regulator of CDC2/cyclin A. In addition, the C-terminal kinase domain binds to its own N-terminal region, suggesting potential negative regulation through interference with complex formation via intramolecular binding. Biochemical and genetic data suggest a role as a tumor suppressor. This is supported by studies in knockout mice showing development of soft-tissue sarcomas, ovarian stromal cell tumors and a high sensitivity to carcinogenic treatments. [provided by RefSeq, Apr 2017]","start":149658153,"end":149718256,"strand":-1,"description":"large tumor suppressor kinase 1 [Source:HGNC Symbol;Acc:HGNC:6514]"}, {"versioned_ensembl_gene_id":"ENSG00000106771.12","gene_symbol":"TMEM245","gene_name":"transmembrane protein 245 [Source:HGNC Symbol;Acc:HGNC:1363]","synonyms":"CG-2,C9orf5","biotype":"protein_coding","ncbi_id":"23731","summary":null,"start":109015152,"end":109119945,"strand":-1,"description":"transmembrane protein 245 [Source:HGNC Symbol;Acc:HGNC:1363]"}, {"versioned_ensembl_gene_id":"ENSG00000113068.9","gene_symbol":"PFDN1","gene_name":"prefoldin subunit 1 [Source:HGNC Symbol;Acc:HGNC:8866]","synonyms":"PFD1","biotype":"protein_coding","ncbi_id":"5201","summary":"This gene encodes a member of the prefoldin beta subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. [provided by RefSeq, Jul 2008]","start":140245039,"end":140303121,"strand":-1,"description":"prefoldin subunit 1 [Source:HGNC Symbol;Acc:HGNC:8866]"}, {"versioned_ensembl_gene_id":"ENSG00000230339.2","gene_symbol":"AC015818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20554137,"end":20554380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188770.9","gene_symbol":"OPTC","gene_name":"opticin [Source:HGNC Symbol;Acc:HGNC:8158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26254","summary":"Opticin belongs to class III of the small leucine-rich repeat protein (SLRP) family. Members of this family are typically associated with the extracellular matrix. Opticin is present in significant quantities in the vitreous of the eye and also localizes to the cornea, iris, ciliary body, optic nerve, choroid, retina, and fetal liver. Opticin may noncovalently bind collagen fibrils and regulate fibril morphology, spacing, and organization. The opticin gene is mapped to a region of chromosome 1 that is associated with the inherited eye diseases age-related macular degeneration (AMD) and posterior column ataxia with retinosa pigmentosa (AXPC1). [provided by RefSeq, Jul 2008]","start":203494143,"end":203508864,"strand":1,"description":"opticin [Source:HGNC Symbol;Acc:HGNC:8158]"}, {"versioned_ensembl_gene_id":"ENSG00000250069.1","gene_symbol":"AC011379.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":140200163,"end":140203187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254363.6","gene_symbol":"AC011379.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":140157319,"end":140173051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272081.1","gene_symbol":"AC008972.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72955206,"end":72955699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269469.1","gene_symbol":"AC010619.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49462752,"end":49486231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229983.1","gene_symbol":"AL606468.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212168207,"end":212190259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187866.8","gene_symbol":"FAM122A","gene_name":"family with sequence similarity 122A [Source:HGNC Symbol;Acc:HGNC:23490]","synonyms":"MGC17347,C9orf42","biotype":"protein_coding","ncbi_id":"116224","summary":null,"start":68780034,"end":68784608,"strand":1,"description":"family with sequence similarity 122A [Source:HGNC Symbol;Acc:HGNC:23490]"}, {"versioned_ensembl_gene_id":"ENSG00000013392.7","gene_symbol":"RWDD2A","gene_name":"RWD domain containing 2A [Source:HGNC Symbol;Acc:HGNC:21385]","synonyms":"RWDD2,MGC13523,dJ747H23.2","biotype":"protein_coding","ncbi_id":"112611","summary":null,"start":83193379,"end":83198932,"strand":1,"description":"RWD domain containing 2A [Source:HGNC Symbol;Acc:HGNC:21385]"}, {"versioned_ensembl_gene_id":"ENSG00000262313.1","gene_symbol":"AC127496.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80940418,"end":80942033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104872.10","gene_symbol":"PIH1D1","gene_name":"PIH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26075]","synonyms":"NOP17,FLJ20643","biotype":"protein_coding","ncbi_id":"55011","summary":null,"start":49446298,"end":49453497,"strand":-1,"description":"PIH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26075]"}, {"versioned_ensembl_gene_id":"ENSG00000259586.1","gene_symbol":"AC015712.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100846604,"end":100846767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213741.9","gene_symbol":"RPS29","gene_name":"ribosomal protein S29 [Source:HGNC Symbol;Acc:HGNC:10419]","synonyms":"S29","biotype":"protein_coding","ncbi_id":"6235","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit and a member of the S14P family of ribosomal proteins. The protein, which contains a C2-C2 zinc finger-like domain that can bind to zinc, can enhance the tumor suppressor activity of Ras-related protein 1A (KREV1). It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2013]","start":49570984,"end":49599164,"strand":-1,"description":"ribosomal protein S29 [Source:HGNC Symbol;Acc:HGNC:10419]"}, {"versioned_ensembl_gene_id":"ENSG00000278009.1","gene_symbol":"AL139099.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49601011,"end":49601124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114491.13","gene_symbol":"UMPS","gene_name":"uridine monophosphate synthetase [Source:HGNC Symbol;Acc:HGNC:12563]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7372","summary":"This gene encodes a uridine 5'-monophosphate synthase. The encoded protein is a bifunctional enzyme that catalyzes the final two steps of the de novo pyrimidine biosynthetic pathway. The first reaction is carried out by the N-terminal enzyme orotate phosphoribosyltransferase which converts orotic acid to orotidine-5'-monophosphate. The terminal reaction is carried out by the C-terminal enzyme OMP decarboxylase which converts orotidine-5'-monophosphate to uridine monophosphate. Defects in this gene are the cause of hereditary orotic aciduria. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":124730366,"end":124749273,"strand":1,"description":"uridine monophosphate synthetase [Source:HGNC Symbol;Acc:HGNC:12563]"}, {"versioned_ensembl_gene_id":"ENSG00000145819.15","gene_symbol":"ARHGAP26","gene_name":"Rho GTPase activating protein 26 [Source:HGNC Symbol;Acc:HGNC:17073]","synonyms":"OPHN1L1,OPHN1L,KIAA0621,GRAF","biotype":"protein_coding","ncbi_id":"23092","summary":"Interaction of a cell with the extracellular matrix triggers integrin cell surface receptors to begin signaling cascades that regulate the organization of the actin-cytoskeleton. One of the proteins involved in these cascades is focal adhesion kinase. The protein encoded by this gene is a GTPase activating protein that binds to focal adhesion kinase and mediates the activity of the GTP binding proteins RhoA and Cdc42. Defects in this gene are a cause of juvenile myelomonocytic leukemia (JMML). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2017]","start":142770384,"end":143229011,"strand":1,"description":"Rho GTPase activating protein 26 [Source:HGNC Symbol;Acc:HGNC:17073]"}, {"versioned_ensembl_gene_id":"ENSG00000250056.5","gene_symbol":"LINC01018","gene_name":"long intergenic non-protein coding RNA 1018 [Source:HGNC Symbol;Acc:HGNC:27394]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255167","summary":null,"start":6582136,"end":6588499,"strand":1,"description":"long intergenic non-protein coding RNA 1018 [Source:HGNC Symbol;Acc:HGNC:27394]"}, {"versioned_ensembl_gene_id":"ENSG00000262580.5","gene_symbol":"AC087741.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80200673,"end":80205949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271230.1","gene_symbol":"AC027334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6532891,"end":6533200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225864.1","gene_symbol":"AL645939.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29722981,"end":29723971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141570.10","gene_symbol":"CBX8","gene_name":"chromobox 8 [Source:HGNC Symbol;Acc:HGNC:15962]","synonyms":"RC1,PC3,HPC3","biotype":"protein_coding","ncbi_id":"57332","summary":null,"start":79792132,"end":79801683,"strand":-1,"description":"chromobox 8 [Source:HGNC Symbol;Acc:HGNC:15962]"}, {"versioned_ensembl_gene_id":"ENSG00000250347.1","gene_symbol":"AC005740.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142036707,"end":142037125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231534.1","gene_symbol":"FBXO36-IT1","gene_name":"FBXO36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41489]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874344","summary":null,"start":229942728,"end":229945137,"strand":1,"description":"FBXO36 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41489]"}, {"versioned_ensembl_gene_id":"ENSG00000227638.2","gene_symbol":"HNRNPA1P14","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39132]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421351","summary":null,"start":88410529,"end":88411463,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39132]"}, {"versioned_ensembl_gene_id":"ENSG00000152253.8","gene_symbol":"SPC25","gene_name":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]","synonyms":"AD024,SPBC25,MGC22228","biotype":"protein_coding","ncbi_id":"57405","summary":"This gene encodes a protein that may be involved in kinetochore-microtubule interaction and spindle checkpoint activity. [provided by RefSeq, Jul 2008]","start":168834132,"end":168913371,"strand":-1,"description":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]"}, {"versioned_ensembl_gene_id":"ENSG00000276182.1","gene_symbol":"AL163051.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":96537170,"end":96537904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258601.1","gene_symbol":"AL162464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36808871,"end":36828729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116977.18","gene_symbol":"LGALS8","gene_name":"galectin 8 [Source:HGNC Symbol;Acc:HGNC:6569]","synonyms":"PCTA-1","biotype":"protein_coding","ncbi_id":"3964","summary":"This gene encodes a member of the galectin family. Galectins are beta-galactoside-binding animal lectins with conserved carbohydrate recognition domains. The galectins have been implicated in many essential functions including development, differentiation, cell-cell adhesion, cell-matrix interaction, growth regulation, apoptosis, and RNA splicing. This gene is widely expressed in tumoral tissues and seems to be involved in integrin-like cell interactions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":236518000,"end":236552981,"strand":1,"description":"galectin 8 [Source:HGNC Symbol;Acc:HGNC:6569]"}, {"versioned_ensembl_gene_id":"ENSG00000261266.2","gene_symbol":"AC008870.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23687049,"end":23687689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228485.1","gene_symbol":"GRK5-IT1","gene_name":"GRK5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49478]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"101927868","summary":null,"start":119208531,"end":119211760,"strand":1,"description":"GRK5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:49478]"}, {"versioned_ensembl_gene_id":"ENSG00000248385.7","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069895,"end":54081365,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000167123.18","gene_symbol":"CERCAM","gene_name":"cerebral endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:23723]","synonyms":"GLT25D3,CerCAM,CEECAM1","biotype":"protein_coding","ncbi_id":"51148","summary":null,"start":128411751,"end":128437351,"strand":1,"description":"cerebral endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:23723]"}, {"versioned_ensembl_gene_id":"ENSG00000258301.3","gene_symbol":"VASH1-AS1","gene_name":"VASH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53215]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506603","summary":null,"start":76781733,"end":76786724,"strand":-1,"description":"VASH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53215]"}, {"versioned_ensembl_gene_id":"ENSG00000254997.3","gene_symbol":"KRTAP5-9","gene_name":"keratin associated protein 5-9 [Source:HGNC Symbol;Acc:HGNC:23604]","synonyms":"KRTAP5.9,KRTAP5-1,KRN1","biotype":"protein_coding","ncbi_id":"3846","summary":null,"start":71548418,"end":71549553,"strand":1,"description":"keratin associated protein 5-9 [Source:HGNC Symbol;Acc:HGNC:23604]"}, {"versioned_ensembl_gene_id":"ENSG00000186567.12","gene_symbol":"CEACAM19","gene_name":"carcinoembryonic antigen related cell adhesion molecule 19 [Source:HGNC Symbol;Acc:HGNC:31951]","synonyms":"CEAL1","biotype":"protein_coding","ncbi_id":"56971","summary":null,"start":44662278,"end":44684359,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 19 [Source:HGNC Symbol;Acc:HGNC:31951]"}, {"versioned_ensembl_gene_id":"ENSG00000272367.1","gene_symbol":"AC018754.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87376256,"end":87377180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100592.15","gene_symbol":"DAAM1","gene_name":"dishevelled associated activator of morphogenesis 1 [Source:HGNC Symbol;Acc:HGNC:18142]","synonyms":"KIAA0666","biotype":"protein_coding","ncbi_id":"23002","summary":"Cell motility, adhesion, cytokinesis, and other functions of the cell cortex are mediated by reorganization of the actin cytoskeleton and several formin homology (FH) proteins have been associated with these processes. The protein encoded by this gene contains two FH domains and belongs to a novel FH protein subfamily implicated in cell polarity. A key regulator of cytoskeletal architecture, the small GTPase Rho, is activated during development by Wnt/Fz signaling to control cell polarity and movement. The protein encoded by this gene is thought to function as a scaffolding protein for the Wnt-induced assembly of a disheveled (Dvl)-Rho complex. This protein also promotes the nucleation and elongation of new actin filaments and regulates cell growth through the stabilization of microtubules. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2012]","start":59188646,"end":59371405,"strand":1,"description":"dishevelled associated activator of morphogenesis 1 [Source:HGNC Symbol;Acc:HGNC:18142]"}, {"versioned_ensembl_gene_id":"ENSG00000184640.17","gene_symbol":"SEPT9","gene_name":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]","synonyms":"MSF1,MSF,KIAA0991,AF17q25,SeptD1,PNUTL4","biotype":"protein_coding","ncbi_id":"10801","summary":"This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]","start":77280569,"end":77500596,"strand":1,"description":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]"}, {"versioned_ensembl_gene_id":"ENSG00000108852.14","gene_symbol":"MPP2","gene_name":"membrane palmitoylated protein 2 [Source:HGNC Symbol;Acc:HGNC:7220]","synonyms":"DLG2,DKFZp761D0712","biotype":"protein_coding","ncbi_id":"4355","summary":" Palmitoylated membrane protein 2 is a member of a family of membrane-associated proteins termed MAGUKs (membrane-associated guanylate kinase homologs). MAGUKs interact with the cytoskeleton and regulate cell proliferation, signaling pathways, and intracellular junctions. Palmitoylated membrane protein 2 contains a conserved sequence, called the SH3 (src homology 3) motif, found in several other proteins that associate with the cytoskeleton and are suspected to play important roles in signal transduction. [provided by RefSeq, Jul 2008]","start":43875357,"end":43909711,"strand":-1,"description":"membrane palmitoylated protein 2 [Source:HGNC Symbol;Acc:HGNC:7220]"}, {"versioned_ensembl_gene_id":"ENSG00000262881.1","gene_symbol":"CR936218.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45907670,"end":45910779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124920.13","gene_symbol":"MYRF","gene_name":"myelin regulatory factor [Source:HGNC Symbol;Acc:HGNC:1181]","synonyms":"pqn-47,Ndt80,MRF,C11orf9","biotype":"protein_coding","ncbi_id":"745","summary":"This gene encodes a transcription factor that is required for central nervous system myelination and may regulate oligodendrocyte differentiation. It is thought to act by increasing the expression of genes that effect myelin production but may also directly promote myelin gene expression. Loss of a similar gene in mouse models results in severe demyelination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":61752642,"end":61788518,"strand":1,"description":"myelin regulatory factor [Source:HGNC Symbol;Acc:HGNC:1181]"}, {"versioned_ensembl_gene_id":"ENSG00000164761.8","gene_symbol":"TNFRSF11B","gene_name":"TNF receptor superfamily member 11b [Source:HGNC Symbol;Acc:HGNC:11909]","synonyms":"TR1,OPG,OCIF","biotype":"protein_coding","ncbi_id":"4982","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein is an osteoblast-secreted decoy receptor that functions as a negative regulator of bone resorption. This protein specifically binds to its ligand, osteoprotegerin ligand, both of which are key extracellular regulators of osteoclast development. Studies of the mouse counterpart also suggest that this protein and its ligand play a role in lymph-node organogenesis and vascular calcification. Alternatively spliced transcript variants of this gene have been reported, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":118923557,"end":118952200,"strand":-1,"description":"TNF receptor superfamily member 11b [Source:HGNC Symbol;Acc:HGNC:11909]"}, {"versioned_ensembl_gene_id":"ENSG00000232514.1","gene_symbol":"AL356968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48497263,"end":48497736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254979.5","gene_symbol":"AP000781.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57387365,"end":57424059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205835.8","gene_symbol":"GMNC","gene_name":"geminin coiled-coil domain containing [Source:HGNC Symbol;Acc:HGNC:40049]","synonyms":"GEMC1","biotype":"protein_coding","ncbi_id":"647309","summary":null,"start":190852877,"end":190892429,"strand":-1,"description":"geminin coiled-coil domain containing [Source:HGNC Symbol;Acc:HGNC:40049]"}, {"versioned_ensembl_gene_id":"ENSG00000234848.1","gene_symbol":"AC008758.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12450935,"end":12460705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236483.1","gene_symbol":"MTND2P40","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52084]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075280","summary":null,"start":12502675,"end":12504106,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52084]"}, {"versioned_ensembl_gene_id":"ENSG00000214147.2","gene_symbol":"AC092952.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190830965,"end":190832173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235401.1","gene_symbol":"AL935156.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215267,"end":29216210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218297.2","gene_symbol":"AL935156.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181515,"end":29182450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227334.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30341216,"end":30341350,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000255289.1","gene_symbol":"AC068389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60660820,"end":60664530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229267.2","gene_symbol":"AC016708.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":214810229,"end":214963274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107581.12","gene_symbol":"EIF3A","gene_name":"eukaryotic translation initiation factor 3 subunit A [Source:HGNC Symbol;Acc:HGNC:3271]","synonyms":"TIF32,KIAA0139,EIF3S10,eIF3a,eIF3-theta,eIF3-p170,EIF3","biotype":"protein_coding","ncbi_id":"8661","summary":null,"start":119033670,"end":119080823,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit A [Source:HGNC Symbol;Acc:HGNC:3271]"}, {"versioned_ensembl_gene_id":"ENSG00000167642.12","gene_symbol":"SPINT2","gene_name":"serine peptidase inhibitor, Kunitz type 2 [Source:HGNC Symbol;Acc:HGNC:11247]","synonyms":"Kop,HAI-2","biotype":"protein_coding","ncbi_id":"10653","summary":"This gene encodes a transmembrane protein with two extracellular Kunitz domains that inhibits a variety of serine proteases. The protein inhibits HGF activator which prevents the formation of active hepatocyte growth factor. This gene is a putative tumor suppressor, and mutations in this gene result in congenital sodium diarrhea. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":38244035,"end":38292614,"strand":1,"description":"serine peptidase inhibitor, Kunitz type 2 [Source:HGNC Symbol;Acc:HGNC:11247]"}, {"versioned_ensembl_gene_id":"ENSG00000149136.8","gene_symbol":"SSRP1","gene_name":"structure specific recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:11327]","synonyms":"FACT80","biotype":"protein_coding","ncbi_id":"6749","summary":"The protein encoded by this gene is a subunit of a heterodimer that, along with SUPT16H, forms chromatin transcriptional elongation factor FACT. FACT interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT and cisplatin-damaged DNA may be crucial to the anticancer mechanism of cisplatin. This encoded protein contains a high mobility group box which most likely constitutes the structure recognition element for cisplatin-modified DNA. This protein also functions as a co-activator of the transcriptional activator p63. An alternatively spliced transcript variant of this gene has been described, but its full-length nature is not known. [provided by RefSeq, Jul 2008]","start":57325985,"end":57335877,"strand":-1,"description":"structure specific recognition protein 1 [Source:HGNC Symbol;Acc:HGNC:11327]"}, {"versioned_ensembl_gene_id":"ENSG00000128563.13","gene_symbol":"PRKRIP1","gene_name":"PRKR interacting protein 1 (IL11 inducible) [Source:HGNC Symbol;Acc:HGNC:21894]","synonyms":"KRBOX3,FLJ13902,C114","biotype":"protein_coding","ncbi_id":"79706","summary":null,"start":102363872,"end":102426676,"strand":1,"description":"PRKR interacting protein 1 (IL11 inducible) [Source:HGNC Symbol;Acc:HGNC:21894]"}, {"versioned_ensembl_gene_id":"ENSG00000247077.6","gene_symbol":"PGAM5","gene_name":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Source:HGNC Symbol;Acc:HGNC:28763]","synonyms":"MGC5352,BXLBv68","biotype":"protein_coding","ncbi_id":"192111","summary":null,"start":132710819,"end":132722734,"strand":1,"description":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Source:HGNC Symbol;Acc:HGNC:28763]"}, {"versioned_ensembl_gene_id":"ENSG00000167139.8","gene_symbol":"TBC1D21","gene_name":"TBC1 domain family member 21 [Source:HGNC Symbol;Acc:HGNC:28536]","synonyms":"MgcRabGAP,MGC34741","biotype":"protein_coding","ncbi_id":"161514","summary":null,"start":73873608,"end":73889214,"strand":1,"description":"TBC1 domain family member 21 [Source:HGNC Symbol;Acc:HGNC:28536]"}, {"versioned_ensembl_gene_id":"ENSG00000211964.3","gene_symbol":"IGHV3-48","gene_name":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28424","summary":null,"start":106537810,"end":106538344,"strand":-1,"description":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]"}, {"versioned_ensembl_gene_id":"ENSG00000211965.4","gene_symbol":"IGHV3-49","gene_name":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28423","summary":null,"start":106556936,"end":106557477,"strand":-1,"description":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]"}, {"versioned_ensembl_gene_id":"ENSG00000145348.16","gene_symbol":"TBCK","gene_name":"TBC1 domain containing kinase [Source:HGNC Symbol;Acc:HGNC:28261]","synonyms":"MGC16169,HSPC302","biotype":"protein_coding","ncbi_id":"93627","summary":"This gene encodes a protein that contains a protein kinase domain, a Rhodanase-like domain and the Tre-2/Bub2/Cdc16 (TBC) domain. The encoded protein is thought to play a role in actin organization, cell growth and cell proliferation by regulating the mammalian target of the rapamycin (mTOR) signaling pathway. This protein may also be involved in the transcriptional regulation of the components of the mTOR complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":106041599,"end":106321495,"strand":-1,"description":"TBC1 domain containing kinase [Source:HGNC Symbol;Acc:HGNC:28261]"}, {"versioned_ensembl_gene_id":"ENSG00000253509.1","gene_symbol":"AC104393.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41275115,"end":41277003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105352.10","gene_symbol":"CEACAM4","gene_name":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]","synonyms":"CGM7","biotype":"protein_coding","ncbi_id":"1089","summary":null,"start":41618971,"end":41627074,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]"}, {"versioned_ensembl_gene_id":"ENSG00000171720.9","gene_symbol":"HDAC3","gene_name":"histone deacetylase 3 [Source:HGNC Symbol;Acc:HGNC:4854]","synonyms":"RPD3-2,RPD3,HD3","biotype":"protein_coding","ncbi_id":"8841","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to the histone deacetylase/acuc/apha family. It has histone deacetylase activity and represses transcription when tethered to a promoter. It may participate in the regulation of transcription through its binding with the zinc-finger transcription factor YY1. This protein can also down-regulate p53 function and thus modulate cell growth and apoptosis. This gene is regarded as a potential tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":141620876,"end":141636870,"strand":-1,"description":"histone deacetylase 3 [Source:HGNC Symbol;Acc:HGNC:4854]"}, {"versioned_ensembl_gene_id":"ENSG00000229291.1","gene_symbol":"AL139161.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235957879,"end":235971825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272676.1","gene_symbol":"AP001521.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57045091,"end":57045390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225858.1","gene_symbol":"BX295541.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72660470,"end":72660719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279430.1","gene_symbol":"AL590560.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":159910094,"end":159910554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235630.2","gene_symbol":"BX000688.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573828,"end":29574755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101276.14","gene_symbol":"SLC52A3","gene_name":"solute carrier family 52 member 3 [Source:HGNC Symbol;Acc:HGNC:16187]","synonyms":"RFVT3,hRFT2,C20orf54,bA371L19.1","biotype":"protein_coding","ncbi_id":"113278","summary":"This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]","start":760080,"end":776015,"strand":-1,"description":"solute carrier family 52 member 3 [Source:HGNC Symbol;Acc:HGNC:16187]"}, {"versioned_ensembl_gene_id":"ENSG00000260573.2","gene_symbol":"AC007493.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50407666,"end":50522638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227640.2","gene_symbol":"SOX21-AS1","gene_name":"SOX21 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39807]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507533","summary":null,"start":94712716,"end":94716246,"strand":1,"description":"SOX21 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39807]"}, {"versioned_ensembl_gene_id":"ENSG00000246225.6","gene_symbol":"AC006299.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22829380,"end":22945393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249210.1","gene_symbol":"GAPDHP38","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:37792]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729493","summary":null,"start":46558641,"end":46559642,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:37792]"}, {"versioned_ensembl_gene_id":"ENSG00000211956.2","gene_symbol":"IGHV4-34","gene_name":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28395","summary":null,"start":106373663,"end":106374145,"strand":-1,"description":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]"}, {"versioned_ensembl_gene_id":"ENSG00000248790.1","gene_symbol":"AC097103.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139466430,"end":139466795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255359.2","gene_symbol":"CCDC179","gene_name":"coiled-coil domain containing 179 [Source:HGNC Symbol;Acc:HGNC:44653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100500938","summary":null,"start":22846931,"end":22860426,"strand":-1,"description":"coiled-coil domain containing 179 [Source:HGNC Symbol;Acc:HGNC:44653]"}, {"versioned_ensembl_gene_id":"ENSG00000253440.1","gene_symbol":"IGHV3-33-2","gene_name":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28433","summary":null,"start":106369107,"end":106369546,"strand":-1,"description":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]"}, {"versioned_ensembl_gene_id":"ENSG00000196616.13","gene_symbol":"ADH1B","gene_name":"alcohol dehydrogenase 1B (class I), beta polypeptide [Source:HGNC Symbol;Acc:HGNC:250]","synonyms":"ADH2","biotype":"protein_coding","ncbi_id":"125","summary":"The protein encoded by this gene is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. This encoded protein, consisting of several homo- and heterodimers of alpha, beta, and gamma subunits, exhibits high activity for ethanol oxidation and plays a major role in ethanol catabolism. Three genes encoding alpha, beta and gamma subunits are tandemly organized in a genomic segment as a gene cluster. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":99304964,"end":99352760,"strand":-1,"description":"alcohol dehydrogenase 1B (class I), beta polypeptide [Source:HGNC Symbol;Acc:HGNC:250]"}, {"versioned_ensembl_gene_id":"ENSG00000235734.4","gene_symbol":"HMGN1P36","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728851","summary":null,"start":97827248,"end":97827545,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39380]"}, {"versioned_ensembl_gene_id":"ENSG00000160469.16","gene_symbol":"BRSK1","gene_name":"BR serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18994]","synonyms":"KIAA1811","biotype":"protein_coding","ncbi_id":"84446","summary":null,"start":55282072,"end":55312533,"strand":1,"description":"BR serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18994]"}, {"versioned_ensembl_gene_id":"ENSG00000249318.1","gene_symbol":"AC010468.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111265809,"end":111270089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139579.12","gene_symbol":"NABP2","gene_name":"nucleic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28412]","synonyms":"hSSB1,SSB1,SOSS-B1,OBFC2B,MGC2731","biotype":"protein_coding","ncbi_id":"79035","summary":"Single-stranded DNA (ssDNA)-binding proteins, such as OBFC2B, are ubiquitous and essential for a variety of DNA metabolic processes, including replication, recombination, and detection and repair of damage (Richard et al., 2008 [PubMed 18449195]).[supplied by OMIM, Jun 2008]","start":56222015,"end":56229854,"strand":1,"description":"nucleic acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28412]"}, {"versioned_ensembl_gene_id":"ENSG00000115085.13","gene_symbol":"ZAP70","gene_name":"zeta chain of T-cell receptor associated protein kinase 70 [Source:HGNC Symbol;Acc:HGNC:12858]","synonyms":"ZAP-70,STD,SRK","biotype":"protein_coding","ncbi_id":"7535","summary":"This gene encodes an enzyme belonging to the protein tyrosine kinase family, and it plays a role in T-cell development and lymphocyte activation. This enzyme, which is phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn. This enzyme is also essential for thymocyte development. Mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells. Two transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":97713560,"end":97739862,"strand":1,"description":"zeta chain of T-cell receptor associated protein kinase 70 [Source:HGNC Symbol;Acc:HGNC:12858]"}, {"versioned_ensembl_gene_id":"ENSG00000273881.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000115286.19","gene_symbol":"NDUFS7","gene_name":"NADH:ubiquinone oxidoreductase core subunit S7 [Source:HGNC Symbol;Acc:HGNC:7714]","synonyms":"PSST,FLJ46880,FLJ45860,CI-20","biotype":"protein_coding","ncbi_id":"374291","summary":"This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008]","start":1383527,"end":1395589,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S7 [Source:HGNC Symbol;Acc:HGNC:7714]"}, {"versioned_ensembl_gene_id":"ENSG00000283948.1","gene_symbol":"AC247036.7","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106170749,"end":106171052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257863.1","gene_symbol":"AC090049.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91901458,"end":91906187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206515.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"MAS-L,dJ994E9.2,MRG","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486639,"end":29487775,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000278345.1","gene_symbol":"GU182343.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54814919,"end":54820584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111231.8","gene_symbol":"GPN3","gene_name":"GPN-loop GTPase 3 [Source:HGNC Symbol;Acc:HGNC:30186]","synonyms":"MGC14560,ATPBD1C","biotype":"protein_coding","ncbi_id":"51184","summary":null,"start":110452484,"end":110469268,"strand":-1,"description":"GPN-loop GTPase 3 [Source:HGNC Symbol;Acc:HGNC:30186]"}, {"versioned_ensembl_gene_id":"ENSG00000198408.13","gene_symbol":"MGEA5","gene_name":"meningioma expressed antigen 5 (hyaluronidase) [Source:HGNC Symbol;Acc:HGNC:7056]","synonyms":"OGA,NCOAT,MEA5","biotype":"protein_coding","ncbi_id":"10724","summary":"The dynamic modification of cytoplasmic and nuclear proteins by O-linked N-acetylglucosamine (O-GlcNAc) addition and removal on serine and threonine residues is catalyzed by OGT (MIM 300255), which adds O-GlcNAc, and MGEA5, a glycosidase that removes O-GlcNAc modifications (Gao et al., 2001 [PubMed 11148210]).[supplied by OMIM, Mar 2008]","start":101784443,"end":101818465,"strand":-1,"description":"meningioma expressed antigen 5 (hyaluronidase) [Source:HGNC Symbol;Acc:HGNC:7056]"}, {"versioned_ensembl_gene_id":"ENSG00000160584.15","gene_symbol":"SIK3","gene_name":"SIK family kinase 3 [Source:HGNC Symbol;Acc:HGNC:29165]","synonyms":"QSK,L19,KIAA0999,FLJ12240","biotype":"protein_coding","ncbi_id":"23387","summary":null,"start":116843402,"end":117098437,"strand":-1,"description":"SIK family kinase 3 [Source:HGNC Symbol;Acc:HGNC:29165]"}, {"versioned_ensembl_gene_id":"ENSG00000276775.1","gene_symbol":"IGHV4-4","gene_name":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28401","summary":null,"start":106011922,"end":106012420,"strand":-1,"description":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]"}, {"versioned_ensembl_gene_id":"ENSG00000185834.10","gene_symbol":"RPL12P4","gene_name":"ribosomal protein L12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16587]","synonyms":"dJ800C24.1","biotype":"processed_pseudogene","ncbi_id":"116149","summary":null,"start":55074644,"end":55075140,"strand":1,"description":"ribosomal protein L12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16587]"}, {"versioned_ensembl_gene_id":"ENSG00000235038.1","gene_symbol":"AL445193.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58060139,"end":58080274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159176.13","gene_symbol":"CSRP1","gene_name":"cysteine and glycine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2469]","synonyms":"D1S181E,CYRP,CSRP","biotype":"protein_coding","ncbi_id":"1465","summary":"This gene encodes a member of the cysteine-rich protein (CSRP) family. This gene family includes a group of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this gene product occurs in proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2010]","start":201483530,"end":201509456,"strand":-1,"description":"cysteine and glycine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2469]"}, {"versioned_ensembl_gene_id":"ENSG00000230030.1","gene_symbol":"AL353742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108252154,"end":108254820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206646.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68361075,"end":68361187,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000211928.1","gene_symbol":"IGHD5-5","gene_name":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]","synonyms":"IGHD55,DK4","biotype":"IG_D_gene","ncbi_id":"28492","summary":null,"start":105912257,"end":105912276,"strand":-1,"description":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]"}, {"versioned_ensembl_gene_id":"ENSG00000211925.1","gene_symbol":"IGHD2-8","gene_name":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]","synonyms":"IGHD28,DLR1","biotype":"IG_D_gene","ncbi_id":"28504","summary":null,"start":105907211,"end":105907241,"strand":-1,"description":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]"}, {"versioned_ensembl_gene_id":"ENSG00000272663.1","gene_symbol":"AC093635.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48440043,"end":48440597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165669.13","gene_symbol":"FAM204A","gene_name":"family with sequence similarity 204 member A [Source:HGNC Symbol;Acc:HGNC:25794]","synonyms":"FLJ13188,C10orf84,bA319I23.1","biotype":"protein_coding","ncbi_id":"63877","summary":null,"start":118297930,"end":118342328,"strand":-1,"description":"family with sequence similarity 204 member A [Source:HGNC Symbol;Acc:HGNC:25794]"}, {"versioned_ensembl_gene_id":"ENSG00000187772.7","gene_symbol":"LIN28B","gene_name":"lin-28 homolog B [Source:HGNC Symbol;Acc:HGNC:32207]","synonyms":"FLJ16517,CSDD2","biotype":"protein_coding","ncbi_id":"389421","summary":"The protein encoded by this gene belongs to the lin-28 family, which is characterized by the presence of a cold-shock domain and a pair of CCHC zinc finger domains. This gene is highly expressed in testis, fetal liver, placenta, and in primary human tumors and cancer cell lines. It is negatively regulated by microRNAs that target sites in the 3' UTR, and overexpression of this gene in primary tumors is linked to the repression of let-7 family of microRNAs and derepression of let-7 targets, which facilitates cellular transformation. [provided by RefSeq, Jun 2012]","start":104936616,"end":105083332,"strand":1,"description":"lin-28 homolog B [Source:HGNC Symbol;Acc:HGNC:32207]"}, {"versioned_ensembl_gene_id":"ENSG00000180089.5","gene_symbol":"TMEM86B","gene_name":"transmembrane protein 86B [Source:HGNC Symbol;Acc:HGNC:28448]","synonyms":"MGC30208","biotype":"protein_coding","ncbi_id":"255043","summary":null,"start":55226639,"end":55229264,"strand":-1,"description":"transmembrane protein 86B [Source:HGNC Symbol;Acc:HGNC:28448]"}, {"versioned_ensembl_gene_id":"ENSG00000253613.2","gene_symbol":"AC008572.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111076921,"end":111092115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145777.14","gene_symbol":"TSLP","gene_name":"thymic stromal lymphopoietin [Source:HGNC Symbol;Acc:HGNC:30743]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85480","summary":"This gene encodes a hemopoietic cytokine proposed to signal through a heterodimeric receptor complex composed of the thymic stromal lymphopoietin receptor and the IL-7R alpha chain. It mainly impacts myeloid cells and induces the release of T cell-attracting chemokines from monocytes and enhances the maturation of CD11c(+) dendritic cells. The protein promotes T helper type 2 (TH2) cell responses that are associated with immunity in various inflammatory diseases, including asthma, allergic inflammation and chronic obstructive pulmonary disease. The protein is therefore considered a potential therapeutic target for the treatment of such diseases. In addition, the shorter (predominant) isoform is an antimicrobial protein, displaying antibacterial and antifungal activity against B. cereus, E. coli, E. faecalis, S. mitis, S. epidermidis, and C. albicans. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":111070062,"end":111078024,"strand":1,"description":"thymic stromal lymphopoietin [Source:HGNC Symbol;Acc:HGNC:30743]"}, {"versioned_ensembl_gene_id":"ENSG00000197345.12","gene_symbol":"MRPL21","gene_name":"mitochondrial ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:14479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219927","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Multiple transcript variants encoding different isoforms were identified through sequence analysis although some may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Jul 2008]","start":68891276,"end":68903835,"strand":-1,"description":"mitochondrial ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:14479]"}, {"versioned_ensembl_gene_id":"ENSG00000211904.2","gene_symbol":"IGHJ2","gene_name":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28481","summary":null,"start":105865199,"end":105865250,"strand":-1,"description":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]"}, {"versioned_ensembl_gene_id":"ENSG00000211905.1","gene_symbol":"IGHJ1","gene_name":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28483","summary":null,"start":105865407,"end":105865458,"strand":-1,"description":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]"}, {"versioned_ensembl_gene_id":"ENSG00000280776.1","gene_symbol":"AC021079.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161910252,"end":162001196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272195.1","gene_symbol":"AL356512.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":244969350,"end":244971088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189129.13","gene_symbol":"PLAC9","gene_name":"placenta specific 9 [Source:HGNC Symbol;Acc:HGNC:19255]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219348","summary":null,"start":80131682,"end":80145359,"strand":1,"description":"placenta specific 9 [Source:HGNC Symbol;Acc:HGNC:19255]"}, {"versioned_ensembl_gene_id":"ENSG00000254647.6","gene_symbol":"INS","gene_name":"insulin [Source:HGNC Symbol;Acc:HGNC:6081]","synonyms":"IDDM2,IDDM1","biotype":"protein_coding","ncbi_id":"3630","summary":"This gene encodes insulin, a peptide hormone that plays a vital role in the regulation of carbohydrate and lipid metabolism. After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified, including insulin-dependent diabetes mellitus, permanent neonatal diabetes diabetes mellitus, maturity-onset diabetes of the young type 10 and hyperproinsulinemia. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region. [provided by RefSeq, May 2020]","start":2159779,"end":2161341,"strand":-1,"description":"insulin [Source:HGNC Symbol;Acc:HGNC:6081]"}, {"versioned_ensembl_gene_id":"ENSG00000229961.2","gene_symbol":"AL357143.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":157171116,"end":157191963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092094.10","gene_symbol":"OSGEP","gene_name":"O-sialoglycoprotein endopeptidase [Source:HGNC Symbol;Acc:HGNC:18028]","synonyms":"TCS3,PRSMG1,OSGEP1,KAE1,GCPL1","biotype":"protein_coding","ncbi_id":"55644","summary":null,"start":20446411,"end":20455105,"strand":-1,"description":"O-sialoglycoprotein endopeptidase [Source:HGNC Symbol;Acc:HGNC:18028]"}, {"versioned_ensembl_gene_id":"ENSG00000273841.4","gene_symbol":"TAF9","gene_name":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]","synonyms":"MGC5067,MGC3647,MGC1603,CGI-137,TAFIID32,AD-004,TAFII32,TAFII31,TAF2G","biotype":"protein_coding","ncbi_id":"6880","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the smaller subunits of TFIID that binds to the basal transcription factor GTF2B as well as to several transcriptional activators such as p53 and VP16. In human, TAF9 and AK6 (GeneID: 102157402) are two distinct genes that share 5' exons. A similar but distinct gene (TAF9L) has been found on the X chromosome and a pseudogene has been identified on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":69364743,"end":69370013,"strand":-1,"description":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]"}, {"versioned_ensembl_gene_id":"ENSG00000231582.2","gene_symbol":"MTND4LP21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075306","summary":null,"start":235541412,"end":235541706,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]"}, {"versioned_ensembl_gene_id":"ENSG00000267144.1","gene_symbol":"AC067968.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44023604,"end":44025262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010319.6","gene_symbol":"SEMA3G","gene_name":"semaphorin 3G [Source:HGNC Symbol;Acc:HGNC:30400]","synonyms":"sem2,FLJ00014","biotype":"protein_coding","ncbi_id":"56920","summary":"The transcription of this gene is activated by PPAR-gamma, and the resulting protein product plays a role in endothelial cell migration. Expression of this gene also inhibits tumor cell migration and invasion. [provided by RefSeq, Jul 2016]","start":52433053,"end":52445085,"strand":-1,"description":"semaphorin 3G [Source:HGNC Symbol;Acc:HGNC:30400]"}, {"versioned_ensembl_gene_id":"ENSG00000229644.6","gene_symbol":"NAMPTP1","gene_name":"nicotinamide phosphoribosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17633]","synonyms":"PBEF2,NAMPTL,bA92J19.4","biotype":"processed_pseudogene","ncbi_id":"646309","summary":null,"start":36521721,"end":36524234,"strand":-1,"description":"nicotinamide phosphoribosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17633]"}, {"versioned_ensembl_gene_id":"ENSG00000260740.2","gene_symbol":"AC026471.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31487370,"end":31488492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110852.4","gene_symbol":"CLEC2B","gene_name":"C-type lectin domain family 2 member B [Source:HGNC Symbol;Acc:HGNC:2053]","synonyms":"HP10085,CLECSF2,AICL","biotype":"protein_coding","ncbi_id":"9976","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell activation antigen. An alternative splice variant has been described but its full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":9852984,"end":9870136,"strand":-1,"description":"C-type lectin domain family 2 member B [Source:HGNC Symbol;Acc:HGNC:2053]"}, {"versioned_ensembl_gene_id":"ENSG00000271420.1","gene_symbol":"AL109936.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23378380,"end":23379029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253537.2","gene_symbol":"PCDHGA7","gene_name":"protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:HGNC:8705]","synonyms":"PCDH-GAMMA-A7","biotype":"protein_coding","ncbi_id":"56108","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141382739,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:HGNC:8705]"}, {"versioned_ensembl_gene_id":"ENSG00000226473.2","gene_symbol":"AC079807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47939738,"end":47940218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272456.1","gene_symbol":"AC087045.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134722947,"end":134723949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220556.4","gene_symbol":"AL035690.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39039603,"end":39039985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167612.12","gene_symbol":"ANKRD33","gene_name":"ankyrin repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:13788]","synonyms":"PANKY,DKFZp686O1689,C12orf7","biotype":"protein_coding","ncbi_id":"341405","summary":null,"start":51887960,"end":51891664,"strand":1,"description":"ankyrin repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:13788]"}, {"versioned_ensembl_gene_id":"ENSG00000173868.11","gene_symbol":"PHOSPHO1","gene_name":"phosphoethanolamine/phosphocholine phosphatase [Source:HGNC Symbol;Acc:HGNC:16815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"162466","summary":null,"start":49223362,"end":49230766,"strand":-1,"description":"phosphoethanolamine/phosphocholine phosphatase [Source:HGNC Symbol;Acc:HGNC:16815]"}, {"versioned_ensembl_gene_id":"ENSG00000227475.1","gene_symbol":"AL355300.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36089086,"end":36089389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235195.1","gene_symbol":"AL929561.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071811,"end":29072586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275545.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54746462,"end":54760779,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000211891.6","gene_symbol":"IGHE","gene_name":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3497","summary":null,"start":105597691,"end":105601728,"strand":-1,"description":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]"}, {"versioned_ensembl_gene_id":"ENSG00000233527.8","gene_symbol":"ZNF529-AS1","gene_name":"ZNF529 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51275]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927599","summary":null,"start":36573070,"end":36594708,"strand":1,"description":"ZNF529 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51275]"}, {"versioned_ensembl_gene_id":"ENSG00000161298.17","gene_symbol":"ZNF382","gene_name":"zinc finger protein 382 [Source:HGNC Symbol;Acc:HGNC:17409]","synonyms":"KS1,FLJ14686","biotype":"protein_coding","ncbi_id":"84911","summary":"This gene encodes a KRAB domain zinc finger transcription factor (KZNF). KZNFs play critical roles in the regulation of many cellular processes including differentiation, proliferation and apoptosis. The encoded protein inhibits activating protein 1 (AP-1) and nuclear factor kappa-B (NF-kB) signaling and may function as a tumor suppressor in multiple carcinomas. This gene is found in a cluster with other zinc finger protein genes on the long arm of chromosome 19, and alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":36604817,"end":36634113,"strand":1,"description":"zinc finger protein 382 [Source:HGNC Symbol;Acc:HGNC:17409]"}, {"versioned_ensembl_gene_id":"ENSG00000240724.2","gene_symbol":"AP002852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102503753,"end":102504137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271612.1","gene_symbol":"HSPE1P14","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481674","summary":null,"start":102451763,"end":102452483,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49333]"}, {"versioned_ensembl_gene_id":"ENSG00000207403.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121378797,"end":121378898,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000259004.1","gene_symbol":"LINC02285","gene_name":"long intergenic non-protein coding RNA 2285 [Source:HGNC Symbol;Acc:HGNC:53202]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929422","summary":null,"start":101120856,"end":101123542,"strand":1,"description":"long intergenic non-protein coding RNA 2285 [Source:HGNC Symbol;Acc:HGNC:53202]"}, {"versioned_ensembl_gene_id":"ENSG00000223547.9","gene_symbol":"ZNF844","gene_name":"zinc finger protein 844 [Source:HGNC Symbol;Acc:HGNC:25932]","synonyms":"FLJ14959","biotype":"protein_coding","ncbi_id":"284391","summary":null,"start":12064699,"end":12081565,"strand":1,"description":"zinc finger protein 844 [Source:HGNC Symbol;Acc:HGNC:25932]"}, {"versioned_ensembl_gene_id":"ENSG00000204920.10","gene_symbol":"ZNF155","gene_name":"zinc finger protein 155 [Source:HGNC Symbol;Acc:HGNC:12940]","synonyms":"pHZ-96","biotype":"protein_coding","ncbi_id":"7711","summary":null,"start":43967862,"end":43998325,"strand":1,"description":"zinc finger protein 155 [Source:HGNC Symbol;Acc:HGNC:12940]"}, {"versioned_ensembl_gene_id":"ENSG00000277560.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786463,"end":54790318,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000223358.5","gene_symbol":"EHHADH-AS1","gene_name":"EHHADH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44133]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"339926","summary":null,"start":185162871,"end":185191955,"strand":1,"description":"EHHADH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44133]"}, {"versioned_ensembl_gene_id":"ENSG00000183251.4","gene_symbol":"OR51B4","gene_name":"olfactory receptor family 51 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:14708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79339","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5301014,"end":5301946,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:14708]"}, {"versioned_ensembl_gene_id":"ENSG00000251173.1","gene_symbol":"UCHL1-AS1","gene_name":"UCHL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40600]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410542","summary":null,"start":41220074,"end":41256727,"strand":-1,"description":"UCHL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40600]"}, {"versioned_ensembl_gene_id":"ENSG00000154134.14","gene_symbol":"ROBO3","gene_name":"roundabout guidance receptor 3 [Source:HGNC Symbol;Acc:HGNC:13433]","synonyms":"RBIG1,HGPS,HGPPS,FLJ21044","biotype":"protein_coding","ncbi_id":"64221","summary":"This gene is a member of the Roundabout (ROBO) gene family that controls neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are a subfamily of the immunoglobulin transmembrane receptor superfamily. SLIT proteins 1-3, a family of secreted chemorepellants, are ligands for ROBO proteins and SLIT/ROBO interactions regulate myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, and vasculogenesis in addition to neurogenesis. This gene, ROBO3, has a putative extracellular domain with five immunoglobulin (Ig)-like loops and three fibronectin (Fn) type III motifs, a transmembrane segment, and a cytoplasmic tail with three conserved signaling motifs: CC0, CC2, and CC3 (CC for conserved cytoplasmic). Unlike other ROBO family members, ROBO3 lacks motif CC1. The ROBO3 gene regulates axonal navigation at the ventral midline of the neural tube. In mouse, loss of Robo3 results in a complete failure of commissural axons to cross the midline throughout the spinal cord and the hindbrain. Mutations ROBO3 result in horizontal gaze palsy with progressive scoliosis (HGPPS); an autosomal recessive disorder characterized by congenital absence of horizontal gaze, progressive scoliosis, and failure of the corticospinal and somatosensory axon tracts to cross the midline in the medulla. [provided by RefSeq, May 2019]","start":124865386,"end":124881470,"strand":1,"description":"roundabout guidance receptor 3 [Source:HGNC Symbol;Acc:HGNC:13433]"}, {"versioned_ensembl_gene_id":"ENSG00000218459.1","gene_symbol":"AL121972.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73618346,"end":73618597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137710.14","gene_symbol":"RDX","gene_name":"radixin [Source:HGNC Symbol;Acc:HGNC:9944]","synonyms":"DFNB24","biotype":"protein_coding","ncbi_id":"5962","summary":"Radixin is a cytoskeletal protein that may be important in linking actin to the plasma membrane. It is highly similar in sequence to both ezrin and moesin. The radixin gene has been localized by fluorescence in situ hybridization to 11q23. A truncated version representing a pseudogene (RDXP2) was assigned to Xp21.3. Another pseudogene that seemed to lack introns (RDXP1) was mapped to 11p by Southern and PCR analyses. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":110174880,"end":110296722,"strand":-1,"description":"radixin [Source:HGNC Symbol;Acc:HGNC:9944]"}, {"versioned_ensembl_gene_id":"ENSG00000270780.1","gene_symbol":"AL591742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114001433,"end":114002235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185515.14","gene_symbol":"BRCC3","gene_name":"BRCA1/BRCA2-containing complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24185]","synonyms":"CXorf53,C6.1A,BRCC36","biotype":"protein_coding","ncbi_id":"79184","summary":"This gene encodes a subunit of the BRCA1-BRCA2-containing complex (BRCC), which is an E3 ubiquitin ligase. This complex plays a role in the DNA damage response, where it is responsible for the stable accumulation of BRCA1 at DNA break sites. The component encoded by this gene can specifically cleave Lys 63-linked polyubiquitin chains, and it regulates the abundance of these polyubiquitin chains in chromatin. The loss of this gene results in abnormal angiogenesis and is associated with syndromic moyamoya, a cerebrovascular angiopathy. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jun 2011]","start":155071420,"end":155123074,"strand":1,"description":"BRCA1/BRCA2-containing complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24185]"}, {"versioned_ensembl_gene_id":"ENSG00000235572.1","gene_symbol":"AL353615.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135352684,"end":135354220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279771.1","gene_symbol":"AP000997.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":115659168,"end":115661417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227958.1","gene_symbol":"AL390778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135204722,"end":135237597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225100.2","gene_symbol":"DPY19L2P5","gene_name":"DPY19L2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480421","summary":null,"start":79982910,"end":79983240,"strand":-1,"description":"DPY19L2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51620]"}, {"versioned_ensembl_gene_id":"ENSG00000188486.3","gene_symbol":"H2AFX","gene_name":"H2A histone family member X [Source:HGNC Symbol;Acc:HGNC:4739]","synonyms":"H2AX","biotype":"protein_coding","ncbi_id":"3014","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the histone H2A family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif. [provided by RefSeq, Oct 2015]","start":119093854,"end":119095467,"strand":-1,"description":"H2A histone family member X [Source:HGNC Symbol;Acc:HGNC:4739]"}, {"versioned_ensembl_gene_id":"ENSG00000187609.15","gene_symbol":"EXD3","gene_name":"exonuclease 3'-5' domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26023]","synonyms":"FLJ20433,mut-7,LOC54932","biotype":"protein_coding","ncbi_id":"54932","summary":null,"start":137306896,"end":137423262,"strand":-1,"description":"exonuclease 3'-5' domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26023]"}, {"versioned_ensembl_gene_id":"ENSG00000267019.1","gene_symbol":"NTF6A","gene_name":"neurotrophin 6 alpha (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8025]","synonyms":"PSI-NT4,NTF6,NTF5P","biotype":"unprocessed_pseudogene","ncbi_id":"4910","summary":null,"start":49025461,"end":49026020,"strand":-1,"description":"neurotrophin 6 alpha (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8025]"}, {"versioned_ensembl_gene_id":"ENSG00000163121.9","gene_symbol":"NEURL3","gene_name":"neuralized E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:25162]","synonyms":"LOC93082,Lincr","biotype":"protein_coding","ncbi_id":"93082","summary":null,"start":96497643,"end":96508109,"strand":-1,"description":"neuralized E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:25162]"}, {"versioned_ensembl_gene_id":"ENSG00000160117.14","gene_symbol":"ANKLE1","gene_name":"ankyrin repeat and LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26812]","synonyms":"LEMD6,FLJ39369,ANKRD41","biotype":"protein_coding","ncbi_id":"126549","summary":null,"start":17281645,"end":17287646,"strand":1,"description":"ankyrin repeat and LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26812]"}, {"versioned_ensembl_gene_id":"ENSG00000267335.2","gene_symbol":"AC008687.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49022953,"end":49036895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280029.3","gene_symbol":"AC244517.11","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141136683,"end":141245380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272108.1","gene_symbol":"AC244517.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141118680,"end":141120765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280336.1","gene_symbol":"AC244517.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141168231,"end":141168893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187372.11","gene_symbol":"PCDHB13","gene_name":"protocadherin beta 13 [Source:HGNC Symbol;Acc:HGNC:8684]","synonyms":"PCDH-BETA13","biotype":"protein_coding","ncbi_id":"56123","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141213919,"end":141218979,"strand":1,"description":"protocadherin beta 13 [Source:HGNC Symbol;Acc:HGNC:8684]"}, {"versioned_ensembl_gene_id":"ENSG00000196136.17","gene_symbol":"SERPINA3","gene_name":"serpin family A member 3 [Source:HGNC Symbol;Acc:HGNC:16]","synonyms":"ACT,AACT","biotype":"protein_coding","ncbi_id":"12","summary":"The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. Polymorphisms in this protein appear to be tissue specific and influence protease targeting. Variations in this protein's sequence have been implicated in Alzheimer's disease, and deficiency of this protein has been associated with liver disease. Mutations have been identified in patients with Parkinson disease and chronic obstructive pulmonary disease. [provided by RefSeq, Jun 2020]","start":94612377,"end":94624055,"strand":1,"description":"serpin family A member 3 [Source:HGNC Symbol;Acc:HGNC:16]"}, {"versioned_ensembl_gene_id":"ENSG00000168434.12","gene_symbol":"COG7","gene_name":"component of oligomeric golgi complex 7 [Source:HGNC Symbol;Acc:HGNC:18622]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91949","summary":"The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]","start":23388493,"end":23453180,"strand":-1,"description":"component of oligomeric golgi complex 7 [Source:HGNC Symbol;Acc:HGNC:18622]"}, {"versioned_ensembl_gene_id":"ENSG00000276447.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54626866,"end":54631219,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000236403.1","gene_symbol":"AL353611.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134937151,"end":134943195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257286.1","gene_symbol":"AC089999.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113185624,"end":113192161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241721.1","gene_symbol":"SUMO1P1","gene_name":"SUMO1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33148]","synonyms":"UBL6,UBL2,PIC1L","biotype":"processed_pseudogene","ncbi_id":"391257","summary":null,"start":53875252,"end":53875557,"strand":-1,"description":"SUMO1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33148]"}, {"versioned_ensembl_gene_id":"ENSG00000171403.9","gene_symbol":"KRT9","gene_name":"keratin 9 [Source:HGNC Symbol;Acc:HGNC:6447]","synonyms":"K9,EPPK,CK-9","biotype":"protein_coding","ncbi_id":"3857","summary":"This gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma. [provided by RefSeq, Jul 2008]","start":41565841,"end":41572058,"strand":-1,"description":"keratin 9 [Source:HGNC Symbol;Acc:HGNC:6447]"}, {"versioned_ensembl_gene_id":"ENSG00000276960.1","gene_symbol":"AL109933.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160755398,"end":160757518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206476.13","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"G7a,VARS2L,DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30897815,"end":30916043,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000114861.18","gene_symbol":"FOXP1","gene_name":"forkhead box P1 [Source:HGNC Symbol;Acc:HGNC:3823]","synonyms":"hFKH1B,12CC4,QRF1,HSPC215","biotype":"protein_coding","ncbi_id":"27086","summary":"This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":70954693,"end":71583989,"strand":-1,"description":"forkhead box P1 [Source:HGNC Symbol;Acc:HGNC:3823]"}, {"versioned_ensembl_gene_id":"ENSG00000254713.2","gene_symbol":"HNRNPA1P72","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:48802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480236","summary":null,"start":84545131,"end":84546846,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:48802]"}, {"versioned_ensembl_gene_id":"ENSG00000224980.1","gene_symbol":"RPL23AP85","gene_name":"ribosomal protein L23a pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:51576]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419650","summary":null,"start":56585612,"end":56586242,"strand":-1,"description":"ribosomal protein L23a pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:51576]"}, {"versioned_ensembl_gene_id":"ENSG00000229297.1","gene_symbol":"AL451140.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106584142,"end":106591952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125450.10","gene_symbol":"NUP85","gene_name":"nucleoporin 85 [Source:HGNC Symbol;Acc:HGNC:8734]","synonyms":"NUP75,FLJ12549","biotype":"protein_coding","ncbi_id":"79902","summary":"This gene encodes a protein component of the Nup107-160 subunit of the nuclear pore complex. Nuclear pore complexes are embedded in the nuclear envelope and promote bidirectional transport of macromolecules between the cytoplasm and nucleus. The encoded protein can also bind to the C-terminus of chemokine (C-C motif) receptor 2 (CCR2) and promote chemotaxis of monocytes, thereby participating in the inflammatory response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":75205659,"end":75235758,"strand":1,"description":"nucleoporin 85 [Source:HGNC Symbol;Acc:HGNC:8734]"}, {"versioned_ensembl_gene_id":"ENSG00000254798.1","gene_symbol":"AP001981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109907004,"end":109907741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226857.1","gene_symbol":"DUTP3","gene_name":"deoxyuridine triphosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39516]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100861485","summary":null,"start":147146342,"end":147146756,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39516]"}, {"versioned_ensembl_gene_id":"ENSG00000205683.11","gene_symbol":"DPF3","gene_name":"double PHD fingers 3 [Source:HGNC Symbol;Acc:HGNC:17427]","synonyms":"FLJ14079,Cerd4,cer-d4,BAF45c","biotype":"protein_coding","ncbi_id":"8110","summary":"This gene encodes a member of the D4 protein family. The encoded protein is a transcription regulator that binds acetylated histones and is a component of the BAF chromatin remodeling complex. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":72619296,"end":72894116,"strand":-1,"description":"double PHD fingers 3 [Source:HGNC Symbol;Acc:HGNC:17427]"}, {"versioned_ensembl_gene_id":"ENSG00000279342.2","gene_symbol":"AP000866.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":124789240,"end":124792818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232391.1","gene_symbol":"RANP2","gene_name":"RAN, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39857]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874191","summary":null,"start":147167344,"end":147167572,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39857]"}, {"versioned_ensembl_gene_id":"ENSG00000254941.1","gene_symbol":"AP000866.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124807822,"end":124808269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230190.1","gene_symbol":"AC005518.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":147671711,"end":147673143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224699.8","gene_symbol":"LAMTOR5-AS1","gene_name":"LAMTOR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40823]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101410535","summary":null,"start":110347116,"end":110443817,"strand":1,"description":"LAMTOR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40823]"}, {"versioned_ensembl_gene_id":"ENSG00000228102.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29748203,"end":29748623,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000260686.1","gene_symbol":"AC008669.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":122832356,"end":122834533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280077.1","gene_symbol":"AL353763.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41012231,"end":41014133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274427.1","gene_symbol":"AC145423.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123515275,"end":123515513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227150.1","gene_symbol":"AL669970.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134552738,"end":134553897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184209.14","gene_symbol":"SNRNP35","gene_name":"small nuclear ribonucleoprotein U11/U12 subunit 35 [Source:HGNC Symbol;Acc:HGNC:30852]","synonyms":"U1SNRNPBP","biotype":"protein_coding","ncbi_id":"11066","summary":"The protein encoded by this gene is a homolog of the U1-snRNP binding protein. The N-terminal half contains a RNA recognition motif and the C-terminal half is rich in Arg/Asp and Arg/Glu dipeptides, which is a characteristic of a variety of splicing factors. This protein is a component of the U11/U12 small nuclear ribonucleoproteins (snRNP) that form part of the U12-type spliceosome. Alternative splicing results in multiple transcript variants encoding two distinct isoforms and representing a non-protein coding variant. [provided by RefSeq, Aug 2013]","start":123457641,"end":123473154,"strand":1,"description":"small nuclear ribonucleoprotein U11/U12 subunit 35 [Source:HGNC Symbol;Acc:HGNC:30852]"}, {"versioned_ensembl_gene_id":"ENSG00000188986.6","gene_symbol":"NELFB","gene_name":"negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]","synonyms":"NELF-B,KIAA1182,COBRA1","biotype":"protein_coding","ncbi_id":"25920","summary":"NELFB is a subunit of negative elongation factor (NELF), which also includes NELFA (WHSC2; MIM 606026), either NELFC or NELFD (TH1L; MIM 605297), and NELFE (RDBP; MIM 154040). NELF acts with DRB sensitivity-inducing factor (DSIF), a heterodimer of SPT4 (SUPT4H1; MIM 603555) and SPT5 (SUPT5H; MIM 602102), to cause transcriptional pausing of RNA polymerase II (see MIM 180660) (Narita et al., 2003 [PubMed 12612062]).[supplied by OMIM, Mar 2008]","start":137255173,"end":137273546,"strand":1,"description":"negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]"}, {"versioned_ensembl_gene_id":"ENSG00000162148.10","gene_symbol":"PPP1R32","gene_name":"protein phosphatase 1 regulatory subunit 32 [Source:HGNC Symbol;Acc:HGNC:28869]","synonyms":"IIIG9,FLJ32771,C11orf66","biotype":"protein_coding","ncbi_id":"220004","summary":null,"start":61481120,"end":61490931,"strand":1,"description":"protein phosphatase 1 regulatory subunit 32 [Source:HGNC Symbol;Acc:HGNC:28869]"}, {"versioned_ensembl_gene_id":"ENSG00000250073.2","gene_symbol":"AP000866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124759129,"end":124765936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277778.2","gene_symbol":"PGM5P2","gene_name":"phosphoglucomutase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18965]","synonyms":"AK096159","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"595135","summary":null,"start":41006999,"end":41074617,"strand":-1,"description":"phosphoglucomutase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18965]"}, {"versioned_ensembl_gene_id":"ENSG00000152256.13","gene_symbol":"PDK1","gene_name":"pyruvate dehydrogenase kinase 1 [Source:HGNC Symbol;Acc:HGNC:8809]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5163","summary":"Pyruvate dehydrogenase (PDH) is a mitochondrial multienzyme complex that catalyzes the oxidative decarboxylation of pyruvate and is one of the major enzymes responsible for the regulation of homeostasis of carbohydrate fuels in mammals. The enzymatic activity is regulated by a phosphorylation/dephosphorylation cycle. Phosphorylation of PDH by a specific pyruvate dehydrogenase kinase (PDK) results in inactivation. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2013]","start":172555373,"end":172608669,"strand":1,"description":"pyruvate dehydrogenase kinase 1 [Source:HGNC Symbol;Acc:HGNC:8809]"}, {"versioned_ensembl_gene_id":"ENSG00000273301.1","gene_symbol":"AC016717.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":225698514,"end":225703654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230667.5","gene_symbol":"SETSIP","gene_name":"SET-like protein [Source:HGNC Symbol;Acc:HGNC:42937]","synonyms":"SETP18","biotype":"protein_coding","ncbi_id":"646817","summary":null,"start":92074533,"end":92075441,"strand":-1,"description":"SET-like protein [Source:HGNC Symbol;Acc:HGNC:42937]"}, {"versioned_ensembl_gene_id":"ENSG00000215833.3","gene_symbol":"QRSL1P1","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43667]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730016","summary":null,"start":168449672,"end":168451211,"strand":-1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43667]"}, {"versioned_ensembl_gene_id":"ENSG00000126216.13","gene_symbol":"TUBGCP3","gene_name":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]","synonyms":"GCP3,Spc98p,SPBC98","biotype":"protein_coding","ncbi_id":"10426","summary":null,"start":112485005,"end":112588167,"strand":-1,"description":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]"}, {"versioned_ensembl_gene_id":"ENSG00000256683.6","gene_symbol":"ZNF350","gene_name":"zinc finger protein 350 [Source:HGNC Symbol;Acc:HGNC:16656]","synonyms":"ZFQR,ZBRK1","biotype":"protein_coding","ncbi_id":"59348","summary":null,"start":51964343,"end":51986856,"strand":-1,"description":"zinc finger protein 350 [Source:HGNC Symbol;Acc:HGNC:16656]"}, {"versioned_ensembl_gene_id":"ENSG00000259021.2","gene_symbol":"TPRX1P1","gene_name":"tetrapeptide repeat homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503628","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the TPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":79499666,"end":79499984,"strand":-1,"description":"tetrapeptide repeat homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32176]"}, {"versioned_ensembl_gene_id":"ENSG00000159166.13","gene_symbol":"LAD1","gene_name":"ladinin 1 [Source:HGNC Symbol;Acc:HGNC:6472]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3898","summary":"The protein encoded by this gene may be an anchoring filament that is a component of basement membranes. It may contribute to the stability of the association of the epithelial layers with the underlying mesenchyme. [provided by RefSeq, Jul 2008]","start":201373244,"end":201399915,"strand":-1,"description":"ladinin 1 [Source:HGNC Symbol;Acc:HGNC:6472]"}, {"versioned_ensembl_gene_id":"ENSG00000227722.2","gene_symbol":"AL022100.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":168317497,"end":168376876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276092.1","gene_symbol":"AC040896.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68721082,"end":68721560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165424.6","gene_symbol":"ZCCHC24","gene_name":"zinc finger CCHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:26911]","synonyms":"Z3CXXC8,FLJ90798,C10orf56","biotype":"protein_coding","ncbi_id":"219654","summary":null,"start":79382325,"end":79445627,"strand":-1,"description":"zinc finger CCHC-type containing 24 [Source:HGNC Symbol;Acc:HGNC:26911]"}, {"versioned_ensembl_gene_id":"ENSG00000235426.2","gene_symbol":"AL133481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79382328,"end":79409274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182645.5","gene_symbol":"CCDC172","gene_name":"coiled-coil domain containing 172 [Source:HGNC Symbol;Acc:HGNC:30524]","synonyms":"MGC35062,C10orf96","biotype":"protein_coding","ncbi_id":"374355","summary":null,"start":116324428,"end":116380029,"strand":1,"description":"coiled-coil domain containing 172 [Source:HGNC Symbol;Acc:HGNC:30524]"}, {"versioned_ensembl_gene_id":"ENSG00000235213.1","gene_symbol":"OR6E1P","gene_name":"olfactory receptor family 6 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14739]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79323","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22702143,"end":22703065,"strand":1,"description":"olfactory receptor family 6 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14739]"}, {"versioned_ensembl_gene_id":"ENSG00000107954.10","gene_symbol":"NEURL1","gene_name":"neuralized E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:7761]","synonyms":"h-neu,RNF67,NEURL,neu-1","biotype":"protein_coding","ncbi_id":"9148","summary":null,"start":103493979,"end":103592552,"strand":1,"description":"neuralized E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:7761]"}, {"versioned_ensembl_gene_id":"ENSG00000163933.9","gene_symbol":"RFT1","gene_name":"RFT1 homolog [Source:HGNC Symbol;Acc:HGNC:30220]","synonyms":"CDG1N","biotype":"protein_coding","ncbi_id":"91869","summary":"This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]","start":53088483,"end":53130462,"strand":-1,"description":"RFT1 homolog [Source:HGNC Symbol;Acc:HGNC:30220]"}, {"versioned_ensembl_gene_id":"ENSG00000159202.17","gene_symbol":"UBE2Z","gene_name":"ubiquitin conjugating enzyme E2 Z [Source:HGNC Symbol;Acc:HGNC:25847]","synonyms":"USE1,FLJ13855","biotype":"protein_coding","ncbi_id":"65264","summary":"This gene encodes an enzyme which ubiquitinates proteins which participate in signaling pathways and apoptosis. [provided by RefSeq, Feb 2012]","start":48908369,"end":48929056,"strand":1,"description":"ubiquitin conjugating enzyme E2 Z [Source:HGNC Symbol;Acc:HGNC:25847]"}, {"versioned_ensembl_gene_id":"ENSG00000196704.11","gene_symbol":"AMZ2","gene_name":"archaelysin family metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:28041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51321","summary":"The protein encoded by this gene is a zinc metalloprotease that displays some activity against angiotensin-3. The encoded protein is inhibited by the aminopeptidase inhibitor amastatin, as well as by the general inhibitors o-phenanthroline and batimastat. Defects in this gene may be associated with lung tumorigenesis. [provided by RefSeq, Oct 2016]","start":68247574,"end":68257164,"strand":1,"description":"archaelysin family metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:28041]"}, {"versioned_ensembl_gene_id":"ENSG00000183128.7","gene_symbol":"CALHM3","gene_name":"calcium homeostasis modulator 3 [Source:HGNC Symbol;Acc:HGNC:23458]","synonyms":"FAM26A,bA225H22.7","biotype":"protein_coding","ncbi_id":"119395","summary":null,"start":103472804,"end":103479240,"strand":-1,"description":"calcium homeostasis modulator 3 [Source:HGNC Symbol;Acc:HGNC:23458]"}, {"versioned_ensembl_gene_id":"ENSG00000131095.12","gene_symbol":"GFAP","gene_name":"glial fibrillary acidic protein [Source:HGNC Symbol;Acc:HGNC:4235]","synonyms":"FLJ45472","biotype":"protein_coding","ncbi_id":"2670","summary":"This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":44903161,"end":44916937,"strand":-1,"description":"glial fibrillary acidic protein [Source:HGNC Symbol;Acc:HGNC:4235]"}, {"versioned_ensembl_gene_id":"ENSG00000185933.6","gene_symbol":"CALHM1","gene_name":"calcium homeostasis modulator 1 [Source:HGNC Symbol;Acc:HGNC:23494]","synonyms":"FAM26C","biotype":"protein_coding","ncbi_id":"255022","summary":"This gene encodes a calcium channel that plays a role in processing of amyloid-beta precursor protein. A polymorphism at this locus has been reported to be associated with susceptibility to late-onset Alzheimer's disease in some populations, but the pathogenicity of this polymorphism is unclear.[provided by RefSeq, Mar 2010]","start":103453387,"end":103458888,"strand":-1,"description":"calcium homeostasis modulator 1 [Source:HGNC Symbol;Acc:HGNC:23494]"}, {"versioned_ensembl_gene_id":"ENSG00000214447.4","gene_symbol":"FAM187A","gene_name":"family with sequence similarity 187 member A [Source:HGNC Symbol;Acc:HGNC:35153]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528020","summary":null,"start":44899712,"end":44905390,"strand":1,"description":"family with sequence similarity 187 member A [Source:HGNC Symbol;Acc:HGNC:35153]"}, {"versioned_ensembl_gene_id":"ENSG00000274712.1","gene_symbol":"AC005332.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68205489,"end":68207493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267731.1","gene_symbol":"AC005332.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68189884,"end":68192802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120733.13","gene_symbol":"KDM3B","gene_name":"lysine demethylase 3B [Source:HGNC Symbol;Acc:HGNC:1337]","synonyms":"NET22,KIAA1082,JMJD1B,C5orf7","biotype":"protein_coding","ncbi_id":"51780","summary":null,"start":138352596,"end":138437028,"strand":1,"description":"lysine demethylase 3B [Source:HGNC Symbol;Acc:HGNC:1337]"}, {"versioned_ensembl_gene_id":"ENSG00000267708.1","gene_symbol":"AC005332.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68152776,"end":68159043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163935.13","gene_symbol":"SFMBT1","gene_name":"Scm-like with four mbt domains 1 [Source:HGNC Symbol;Acc:HGNC:20255]","synonyms":"SFMBT,RU1,DKFZp434L243","biotype":"protein_coding","ncbi_id":"51460","summary":"This gene shares high similarity with the Drosophila Scm (sex comb on midleg) gene. It encodes a protein which contains four malignant brain tumor repeat (mbt) domains and may be involved in antigen recognition. [provided by RefSeq, Jun 2012]","start":52903572,"end":53046750,"strand":-1,"description":"Scm-like with four mbt domains 1 [Source:HGNC Symbol;Acc:HGNC:20255]"}, {"versioned_ensembl_gene_id":"ENSG00000267352.1","gene_symbol":"AC005332.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68134675,"end":68135604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174576.9","gene_symbol":"NPAS4","gene_name":"neuronal PAS domain protein 4 [Source:HGNC Symbol;Acc:HGNC:18983]","synonyms":"PASD10,NXF,Le-PAS,bHLHe79","biotype":"protein_coding","ncbi_id":"266743","summary":"NXF is a member of the basic helix-loop-helix-PER (MIM 602260)-ARNT (MIM 126110)-SIM (see SIM2; MIM 600892) (bHLH-PAS) class of transcriptional regulators, which are involved in a wide range of physiologic and developmental events (Ooe et al., 2004 [PubMed 14701734]).[supplied by OMIM, Mar 2008]","start":66421004,"end":66426707,"strand":1,"description":"neuronal PAS domain protein 4 [Source:HGNC Symbol;Acc:HGNC:18983]"}, {"versioned_ensembl_gene_id":"ENSG00000277476.1","gene_symbol":"AC005332.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68133201,"end":68135935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242142.1","gene_symbol":"SERBP1P3","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"553148","summary":null,"start":53064283,"end":53065091,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44630]"}, {"versioned_ensembl_gene_id":"ENSG00000280417.1","gene_symbol":"AC096887.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53046166,"end":53048122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238797.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39441665,"end":39441764,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280721.1","gene_symbol":"LINC01943","gene_name":"long intergenic non-protein coding RNA 1943 [Source:HGNC Symbol;Acc:HGNC:52767]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928173","summary":null,"start":87439523,"end":87459044,"strand":-1,"description":"long intergenic non-protein coding RNA 1943 [Source:HGNC Symbol;Acc:HGNC:52767]"}, {"versioned_ensembl_gene_id":"ENSG00000138777.19","gene_symbol":"PPA2","gene_name":"pyrophosphatase (inorganic) 2 [Source:HGNC Symbol;Acc:HGNC:28883]","synonyms":"FLJ20459","biotype":"protein_coding","ncbi_id":"27068","summary":"The protein encoded by this gene is localized to the mitochondrion, is highly similar to members of the inorganic pyrophosphatase (PPase) family, and contains the signature sequence essential for the catalytic activity of PPase. PPases catalyze the hydrolysis of pyrophosphate to inorganic phosphate, which is important for the phosphate metabolism of cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":105369077,"end":105474081,"strand":-1,"description":"pyrophosphatase (inorganic) 2 [Source:HGNC Symbol;Acc:HGNC:28883]"}, {"versioned_ensembl_gene_id":"ENSG00000272305.5","gene_symbol":"AC096887.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52969119,"end":53099453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276348.1","gene_symbol":"AL353770.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66979132,"end":66988373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267023.5","gene_symbol":"LRRC37A16P","gene_name":"leucine rich repeat containing 37 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:43820]","synonyms":"LRRC37C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"651250","summary":null,"start":68125777,"end":68152468,"strand":-1,"description":"leucine rich repeat containing 37 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:43820]"}, {"versioned_ensembl_gene_id":"ENSG00000264012.1","gene_symbol":"AC091588.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22175465,"end":22176662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224881.1","gene_symbol":"AC068279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87379880,"end":87380767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165480.15","gene_symbol":"SKA3","gene_name":"spindle and kinetochore associated complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20262]","synonyms":"RAMA1,MGC4832,C13orf3","biotype":"protein_coding","ncbi_id":"221150","summary":"This gene encodes a component of the spindle and kinetochore-associated protein complex that regulates microtubule attachment to the kinetochores during mitosis. The encoded protein localizes to the outer kinetechore and may be required for normal chromosome segregation and cell division. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":21153595,"end":21176602,"strand":-1,"description":"spindle and kinetochore associated complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20262]"}, {"versioned_ensembl_gene_id":"ENSG00000213385.3","gene_symbol":"AC105052.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102755146,"end":102755939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173141.4","gene_symbol":"MRPL57","gene_name":"mitochondrial ribosomal protein L57 [Source:HGNC Symbol;Acc:HGNC:14514]","synonyms":"MRP63","biotype":"protein_coding","ncbi_id":"78988","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a protein which belongs to an undetermined ribosomal subunit and which seems to be specific to animal mitoribosomes. Pseudogenes corresponding to this gene are found on chromosomes 1p, 1q, 3p, 5q, 8q, 14q, and Y. [provided by RefSeq, Jul 2008]","start":21176645,"end":21179084,"strand":1,"description":"mitochondrial ribosomal protein L57 [Source:HGNC Symbol;Acc:HGNC:14514]"}, {"versioned_ensembl_gene_id":"ENSG00000265055.1","gene_symbol":"AC145343.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68096046,"end":68101474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275969.2","gene_symbol":"SPATA31A3","gene_name":"SPATA31 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:32003]","synonyms":"DKFZp434B204,OTTHUMG00000013164,FAM75A3","biotype":"protein_coding","ncbi_id":"727830","summary":null,"start":66986304,"end":66992583,"strand":-1,"description":"SPATA31 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:32003]"}, {"versioned_ensembl_gene_id":"ENSG00000244640.1","gene_symbol":"AC096922.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68633706,"end":68634356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131381.12","gene_symbol":"RBSN","gene_name":"rabenosyn, RAB effector [Source:HGNC Symbol;Acc:HGNC:20759]","synonyms":"ZFYVE20","biotype":"protein_coding","ncbi_id":"64145","summary":"This gene encodes a protein that belongs to the FYVE zinc finger family of proteins. The encoded protein interacts with Ras-related proteins that regulate membrane trafficking. A missense mutation in this gene is associated with a defect in the early endocytic pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":15070073,"end":15099163,"strand":-1,"description":"rabenosyn, RAB effector [Source:HGNC Symbol;Acc:HGNC:20759]"}, {"versioned_ensembl_gene_id":"ENSG00000274355.1","gene_symbol":"FAM74A3","gene_name":"family with sequence similarity 74 member A3 [Source:HGNC Symbol;Acc:HGNC:32031]","synonyms":"OTTHUMG00000067149","biotype":"transcribed_processed_pseudogene","ncbi_id":"728495","summary":null,"start":66976520,"end":66976991,"strand":-1,"description":"family with sequence similarity 74 member A3 [Source:HGNC Symbol;Acc:HGNC:32031]"}, {"versioned_ensembl_gene_id":"ENSG00000110975.8","gene_symbol":"SYT10","gene_name":"synaptotagmin 10 [Source:HGNC Symbol;Acc:HGNC:19266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341359","summary":null,"start":33374238,"end":33439819,"strand":-1,"description":"synaptotagmin 10 [Source:HGNC Symbol;Acc:HGNC:19266]"}, {"versioned_ensembl_gene_id":"ENSG00000255794.7","gene_symbol":"RMST","gene_name":"rhabdomyosarcoma 2 associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29893]","synonyms":"NCRNA00054,NCRMS,LINC00054","biotype":"processed_transcript","ncbi_id":"196475","summary":"This gene produces a long non-coding RNA that functions in neurogenesis by aiding in the association of Sox2 transcription factor to its target promoters. [provided by RefSeq, Dec 2017]","start":97430884,"end":97598415,"strand":1,"description":"rhabdomyosarcoma 2 associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29893]"}, {"versioned_ensembl_gene_id":"ENSG00000007520.3","gene_symbol":"TSR3","gene_name":"TSR3, acp transferase ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:14175]","synonyms":"MGC24381,C16orf42","biotype":"protein_coding","ncbi_id":"115939","summary":null,"start":1349240,"end":1351911,"strand":-1,"description":"TSR3, acp transferase ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:14175]"}, {"versioned_ensembl_gene_id":"ENSG00000177189.12","gene_symbol":"RPS6KA3","gene_name":"ribosomal protein S6 kinase A3 [Source:HGNC Symbol;Acc:HGNC:10432]","synonyms":"RSK2,RSK,MRX19,HU-3,CLS","biotype":"protein_coding","ncbi_id":"6197","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Mutations in this gene have been associated with Coffin-Lowry syndrome (CLS). [provided by RefSeq, Jul 2008]","start":20149911,"end":20267100,"strand":-1,"description":"ribosomal protein S6 kinase A3 [Source:HGNC Symbol;Acc:HGNC:10432]"}, {"versioned_ensembl_gene_id":"ENSG00000273584.1","gene_symbol":"AC096708.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68908048,"end":68908599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204849.7","gene_symbol":"SPATA31A1","gene_name":"SPATA31 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:23394]","synonyms":"SPATA31A2,FAM75A2,FAM75A1,DKFZP434B204,C9orf36A,C9orf36","biotype":"protein_coding","ncbi_id":"647060","summary":null,"start":39355669,"end":39361959,"strand":1,"description":"SPATA31 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:23394]"}, {"versioned_ensembl_gene_id":"ENSG00000223730.1","gene_symbol":"Z83838.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":44901547,"end":44902471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233228.1","gene_symbol":"LPCAT2BP","gene_name":"lysophosphatidylcholine acyltransferase 2b, pseudogene [Source:HGNC Symbol;Acc:HGNC:38003]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100128094","summary":null,"start":92066306,"end":92067839,"strand":1,"description":"lysophosphatidylcholine acyltransferase 2b, pseudogene [Source:HGNC Symbol;Acc:HGNC:38003]"}, {"versioned_ensembl_gene_id":"ENSG00000277350.1","gene_symbol":"AL353770.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66942703,"end":66952344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227054.1","gene_symbol":"FDX1P2","gene_name":"ferredoxin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3641]","synonyms":"FDXP2","biotype":"processed_pseudogene","ncbi_id":"2216","summary":null,"start":25692180,"end":25692554,"strand":1,"description":"ferredoxin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3641]"}, {"versioned_ensembl_gene_id":"ENSG00000188186.10","gene_symbol":"LAMTOR4","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 [Source:HGNC Symbol;Acc:HGNC:33772]","synonyms":"C7orf59","biotype":"protein_coding","ncbi_id":"389541","summary":null,"start":100148907,"end":100155944,"strand":1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 [Source:HGNC Symbol;Acc:HGNC:33772]"}, {"versioned_ensembl_gene_id":"ENSG00000143178.12","gene_symbol":"TBX19","gene_name":"T-box 19 [Source:HGNC Symbol;Acc:HGNC:11596]","synonyms":"TPIT,dj747L4.1","biotype":"protein_coding","ncbi_id":"9095","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq, Jul 2008]","start":168281040,"end":168314426,"strand":1,"description":"T-box 19 [Source:HGNC Symbol;Acc:HGNC:11596]"}, {"versioned_ensembl_gene_id":"ENSG00000269066.1","gene_symbol":"AC020908.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17095418,"end":17099307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138172.10","gene_symbol":"CALHM2","gene_name":"calcium homeostasis modulator 2 [Source:HGNC Symbol;Acc:HGNC:23493]","synonyms":"FAM26B","biotype":"protein_coding","ncbi_id":"51063","summary":null,"start":103446786,"end":103452402,"strand":-1,"description":"calcium homeostasis modulator 2 [Source:HGNC Symbol;Acc:HGNC:23493]"}, {"versioned_ensembl_gene_id":"ENSG00000249829.2","gene_symbol":"AC016559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79191549,"end":79191747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163312.10","gene_symbol":"HELQ","gene_name":"helicase, POLQ like [Source:HGNC Symbol;Acc:HGNC:18536]","synonyms":"Hel308","biotype":"protein_coding","ncbi_id":"113510","summary":"HEL308 is a single-stranded DNA-dependent ATPase and DNA helicase (Marini and Wood, 2002 [PubMed 11751861]).[supplied by OMIM, Mar 2008]","start":83407343,"end":83455856,"strand":-1,"description":"helicase, POLQ like [Source:HGNC Symbol;Acc:HGNC:18536]"}, {"versioned_ensembl_gene_id":"ENSG00000254736.1","gene_symbol":"BRD9P1","gene_name":"bromodomain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51445]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481721","summary":null,"start":66389609,"end":66390168,"strand":1,"description":"bromodomain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51445]"}, {"versioned_ensembl_gene_id":"ENSG00000255305.1","gene_symbol":"AP004607.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89978540,"end":89980661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230985.9","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"VARS2L,DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30898953,"end":30917183,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000232406.6","gene_symbol":"AL121895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36148726,"end":36155760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227591.5","gene_symbol":"AL031316.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":209661364,"end":209724125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105559.11","gene_symbol":"PLEKHA4","gene_name":"pleckstrin homology domain containing A4 [Source:HGNC Symbol;Acc:HGNC:14339]","synonyms":"PEPP1","biotype":"protein_coding","ncbi_id":"57664","summary":"This gene encodes a pleckstrin homology (PH) domain-containing protein. The PH domain is found near the N-terminus and contains a putative phosphatidylinositol 3, 4, 5-triphosphate-binding motif (PPBM). Elevated expression of this gene has been observed in some melanomas. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017]","start":48837097,"end":48868632,"strand":-1,"description":"pleckstrin homology domain containing A4 [Source:HGNC Symbol;Acc:HGNC:14339]"}, {"versioned_ensembl_gene_id":"ENSG00000254655.1","gene_symbol":"AP004607.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89960422,"end":89960624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237524.8","gene_symbol":"TEX51","gene_name":"testis expressed 51 [Source:HGNC Symbol;Acc:HGNC:52387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101929926","summary":null,"start":126898882,"end":126902097,"strand":1,"description":"testis expressed 51 [Source:HGNC Symbol;Acc:HGNC:52387]"}, {"versioned_ensembl_gene_id":"ENSG00000172031.6","gene_symbol":"EPHX4","gene_name":"epoxide hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:23758]","synonyms":"FLJ90341,EPHXRP,ABHD7","biotype":"protein_coding","ncbi_id":"253152","summary":null,"start":92029982,"end":92063536,"strand":1,"description":"epoxide hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:23758]"}, {"versioned_ensembl_gene_id":"ENSG00000265758.1","gene_symbol":"LINC01900","gene_name":"long intergenic non-protein coding RNA 1900 [Source:HGNC Symbol;Acc:HGNC:52719]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724208","summary":null,"start":21981121,"end":22051159,"strand":1,"description":"long intergenic non-protein coding RNA 1900 [Source:HGNC Symbol;Acc:HGNC:52719]"}, {"versioned_ensembl_gene_id":"ENSG00000264289.1","gene_symbol":"AC103987.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21914369,"end":21914660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117594.9","gene_symbol":"HSD11B1","gene_name":"hydroxysteroid 11-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5208]","synonyms":"SDR26C1,HSD11B,HSD11","biotype":"protein_coding","ncbi_id":"3290","summary":"The protein encoded by this gene is a microsomal enzyme that catalyzes the conversion of the stress hormone cortisol to the inactive metabolite cortisone. In addition, the encoded protein can catalyze the reverse reaction, the conversion of cortisone to cortisol. Too much cortisol can lead to central obesity, and a particular variation in this gene has been associated with obesity and insulin resistance in children. Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency. Alternate splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, May 2011]","start":209686178,"end":209734950,"strand":1,"description":"hydroxysteroid 11-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5208]"}, {"versioned_ensembl_gene_id":"ENSG00000273123.1","gene_symbol":"AC020634.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123715851,"end":123716399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184887.13","gene_symbol":"BTBD6","gene_name":"BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19897]","synonyms":"BDPL","biotype":"protein_coding","ncbi_id":"90135","summary":null,"start":105248490,"end":105251093,"strand":1,"description":"BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19897]"}, {"versioned_ensembl_gene_id":"ENSG00000250174.5","gene_symbol":"MYLK-AS2","gene_name":"MYLK antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40387]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873940","summary":null,"start":123689644,"end":123692407,"strand":1,"description":"MYLK antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40387]"}, {"versioned_ensembl_gene_id":"ENSG00000242085.1","gene_symbol":"AL928654.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105374618,"end":105374971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078399.17","gene_symbol":"HOXA9","gene_name":"homeobox A9 [Source:HGNC Symbol;Acc:HGNC:5109]","synonyms":"HOX1G,HOX1","biotype":"protein_coding","ncbi_id":"3205","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis. Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene.[provided by RefSeq, Mar 2011]","start":27162435,"end":27175180,"strand":-1,"description":"homeobox A9 [Source:HGNC Symbol;Acc:HGNC:5109]"}, {"versioned_ensembl_gene_id":"ENSG00000261202.1","gene_symbol":"Z83847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40043068,"end":40044530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175699.14","gene_symbol":"CCDC197","gene_name":"coiled-coil domain containing 197 [Source:HGNC Symbol;Acc:HGNC:19860]","synonyms":"c14_5713,C14orf48,LINC00521,C14orf48,LINC00521","biotype":"protein_coding","ncbi_id":"256369","summary":null,"start":93987225,"end":94008863,"strand":1,"description":"coiled-coil domain containing 197 [Source:HGNC Symbol;Acc:HGNC:19860]"}, {"versioned_ensembl_gene_id":"ENSG00000214681.3","gene_symbol":"IQCF5","gene_name":"IQ motif containing F5 [Source:HGNC Symbol;Acc:HGNC:35159]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389124","summary":null,"start":51873721,"end":51875584,"strand":-1,"description":"IQ motif containing F5 [Source:HGNC Symbol;Acc:HGNC:35159]"}, {"versioned_ensembl_gene_id":"ENSG00000184345.4","gene_symbol":"IQCF2","gene_name":"IQ motif containing F2 [Source:HGNC Symbol;Acc:HGNC:31815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389123","summary":null,"start":51861629,"end":51863424,"strand":1,"description":"IQ motif containing F2 [Source:HGNC Symbol;Acc:HGNC:31815]"}, {"versioned_ensembl_gene_id":"ENSG00000214686.4","gene_symbol":"IQCF6","gene_name":"IQ motif containing F6 [Source:HGNC Symbol;Acc:HGNC:35158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440956","summary":null,"start":51778561,"end":51779187,"strand":-1,"description":"IQ motif containing F6 [Source:HGNC Symbol;Acc:HGNC:35158]"}, {"versioned_ensembl_gene_id":"ENSG00000241534.9","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31927837,"end":31934271,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000278011.1","gene_symbol":"AC024941.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88601862,"end":88602195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233767.1","gene_symbol":"PSMA6P3","gene_name":"proteasome subunit alpha 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874510","summary":null,"start":46072085,"end":46072248,"strand":-1,"description":"proteasome subunit alpha 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39608]"}, {"versioned_ensembl_gene_id":"ENSG00000088782.4","gene_symbol":"DEFB127","gene_name":"defensin beta 127 [Source:HGNC Symbol;Acc:HGNC:16206]","synonyms":"DEF-27,C20orf73,bA530N10.2","biotype":"protein_coding","ncbi_id":"140850","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":157470,"end":159163,"strand":1,"description":"defensin beta 127 [Source:HGNC Symbol;Acc:HGNC:16206]"}, {"versioned_ensembl_gene_id":"ENSG00000228235.1","gene_symbol":"AP001476.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46052596,"end":46053105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227165.7","gene_symbol":"WDR11-AS1","gene_name":"WDR11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27437]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283089","summary":null,"start":120761812,"end":120851345,"strand":-1,"description":"WDR11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27437]"}, {"versioned_ensembl_gene_id":"ENSG00000224413.1","gene_symbol":"AP001476.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46037052,"end":46039807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253293.4","gene_symbol":"HOXA10","gene_name":"homeobox A10 [Source:HGNC Symbol;Acc:HGNC:5100]","synonyms":"HOX1H,HOX1","biotype":"protein_coding","ncbi_id":"3206","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor that may regulate gene expression, morphogenesis, and differentiation. More specifically, it may function in fertility, embryo viability, and regulation of hematopoietic lineage commitment. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the downstream homeobox A9 (HOXA9) gene. [provided by RefSeq, Mar 2011]","start":27170591,"end":27180261,"strand":-1,"description":"homeobox A10 [Source:HGNC Symbol;Acc:HGNC:5100]"}, {"versioned_ensembl_gene_id":"ENSG00000253322.1","gene_symbol":"AC104051.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57594166,"end":57805029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253821.1","gene_symbol":"AC090796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57492884,"end":57591559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169710.8","gene_symbol":"FASN","gene_name":"fatty acid synthase [Source:HGNC Symbol;Acc:HGNC:3594]","synonyms":"SDR27X1,FAS","biotype":"protein_coding","ncbi_id":"2194","summary":"The enzyme encoded by this gene is a multifunctional protein. Its main function is to catalyze the synthesis of palmitate from acetyl-CoA and malonyl-CoA, in the presence of NADPH, into long-chain saturated fatty acids. In some cancer cell lines, this protein has been found to be fused with estrogen receptor-alpha (ER-alpha), in which the N-terminus of FAS is fused in-frame with the C-terminus of ER-alpha. [provided by RefSeq, Jul 2008]","start":82078333,"end":82098332,"strand":-1,"description":"fatty acid synthase [Source:HGNC Symbol;Acc:HGNC:3594]"}, {"versioned_ensembl_gene_id":"ENSG00000056487.15","gene_symbol":"PHF21B","gene_name":"PHD finger protein 21B [Source:HGNC Symbol;Acc:HGNC:25161]","synonyms":"PHF4,FLJ34161,BHC80L","biotype":"protein_coding","ncbi_id":"112885","summary":null,"start":44881162,"end":45009999,"strand":-1,"description":"PHD finger protein 21B [Source:HGNC Symbol;Acc:HGNC:25161]"}, {"versioned_ensembl_gene_id":"ENSG00000215480.4","gene_symbol":"OR7E37P","gene_name":"olfactory receptor family 7 subfamily E member 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:8410]","synonyms":"hg533","biotype":"unprocessed_pseudogene","ncbi_id":"100506759","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Mar 2011]","start":41442770,"end":41443666,"strand":1,"description":"olfactory receptor family 7 subfamily E member 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:8410]"}, {"versioned_ensembl_gene_id":"ENSG00000227211.2","gene_symbol":"AL035551.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102615473,"end":102615820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261143.1","gene_symbol":"ADAMTS7P3","gene_name":"ADAMTS7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49409]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400406","summary":null,"start":77976042,"end":77993057,"strand":1,"description":"ADAMTS7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49409]"}, {"versioned_ensembl_gene_id":"ENSG00000235005.1","gene_symbol":"AL450468.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109884176,"end":109886264,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109854.13","gene_symbol":"HTATIP2","gene_name":"HIV-1 Tat interactive protein 2 [Source:HGNC Symbol;Acc:HGNC:16637]","synonyms":"TIP30,SDR44U1,FLJ26963,CC3","biotype":"protein_coding","ncbi_id":"10553","summary":null,"start":20363685,"end":20383783,"strand":1,"description":"HIV-1 Tat interactive protein 2 [Source:HGNC Symbol;Acc:HGNC:16637]"}, {"versioned_ensembl_gene_id":"ENSG00000228420.1","gene_symbol":"LINC01768","gene_name":"long intergenic non-protein coding RNA 1768 [Source:HGNC Symbol;Acc:HGNC:52558]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985167","summary":null,"start":109828355,"end":109871436,"strand":1,"description":"long intergenic non-protein coding RNA 1768 [Source:HGNC Symbol;Acc:HGNC:52558]"}, {"versioned_ensembl_gene_id":"ENSG00000242318.1","gene_symbol":"AC058823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98409290,"end":98409763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257920.1","gene_symbol":"LINC02409","gene_name":"long intergenic non-protein coding RNA 2409 [Source:HGNC Symbol;Acc:HGNC:53338]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369929","summary":null,"start":97272692,"end":97276209,"strand":-1,"description":"long intergenic non-protein coding RNA 2409 [Source:HGNC Symbol;Acc:HGNC:53338]"}, {"versioned_ensembl_gene_id":"ENSG00000254558.1","gene_symbol":"AP005435.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89863848,"end":89865550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204455.7","gene_symbol":"TRIM51BP","gene_name":"tripartite motif-containing 51B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37145]","synonyms":"SPRYD5P1,SPRYD5P","biotype":"unprocessed_pseudogene","ncbi_id":"399937","summary":null,"start":89854953,"end":89862893,"strand":1,"description":"tripartite motif-containing 51B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37145]"}, {"versioned_ensembl_gene_id":"ENSG00000139610.1","gene_symbol":"CELA1","gene_name":"chymotrypsin like elastase family member 1 [Source:HGNC Symbol;Acc:HGNC:3308]","synonyms":"ELA1","biotype":"protein_coding","ncbi_id":"1990","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Unlike other elastases, pancreatic elastase 1 is not expressed in the pancreas. To date, elastase 1 expression has only been detected in skin keratinocytes. Clinical literature that describes human elastase 1 activity in the pancreas or fecal material is actually referring to chymotrypsin-like elastase family, member 3B. [provided by RefSeq, May 2009]","start":51328443,"end":51346679,"strand":-1,"description":"chymotrypsin like elastase family member 1 [Source:HGNC Symbol;Acc:HGNC:3308]"}, {"versioned_ensembl_gene_id":"ENSG00000154727.10","gene_symbol":"GABPA","gene_name":"GA binding protein transcription factor alpha subunit [Source:HGNC Symbol;Acc:HGNC:4071]","synonyms":"NRF2A,NRF2,NFT2,E4TF1A,E4TF1-60","biotype":"protein_coding","ncbi_id":"2551","summary":"This gene encodes one of three GA-binding protein transcription factor subunits which functions as a DNA-binding subunit. Since this subunit shares identity with a subunit encoding the nuclear respiratory factor 2 gene, it is likely involved in activation of cytochrome oxidase expression and nuclear control of mitochondrial function. This subunit also shares identity with a subunit constituting the transcription factor E4TF1, responsible for expression of the adenovirus E4 gene. Because of its chromosomal localization and ability to form heterodimers with other polypeptides, this gene may play a role in the Down Syndrome phenotype. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2010]","start":25734570,"end":25772460,"strand":1,"description":"GA binding protein transcription factor alpha subunit [Source:HGNC Symbol;Acc:HGNC:4071]"}, {"versioned_ensembl_gene_id":"ENSG00000161243.8","gene_symbol":"FBXO27","gene_name":"F-box protein 27 [Source:HGNC Symbol;Acc:HGNC:18753]","synonyms":"Fbx27,Fbg5","biotype":"protein_coding","ncbi_id":"126433","summary":"Members of the F-box protein family, such as FBXO27, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":38990714,"end":39032785,"strand":-1,"description":"F-box protein 27 [Source:HGNC Symbol;Acc:HGNC:18753]"}, {"versioned_ensembl_gene_id":"ENSG00000275155.1","gene_symbol":"AC027348.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49847018,"end":49847632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278455.1","gene_symbol":"AL606534.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":243049782,"end":243051619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234116.1","gene_symbol":"AL606534.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":243005845,"end":243007468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166013.11","gene_symbol":"TRIM53BP","gene_name":"tripartite motif containing 53B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37144]","synonyms":"TRIM80P,TRIM53L,TRIM53B","biotype":"unprocessed_pseudogene","ncbi_id":"642425","summary":null,"start":89841997,"end":89850970,"strand":1,"description":"tripartite motif containing 53B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37144]"}, {"versioned_ensembl_gene_id":"ENSG00000230199.1","gene_symbol":"AL603825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242975005,"end":242975084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277704.1","gene_symbol":"AL445675.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242890247,"end":242890803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266858.1","gene_symbol":"RPSAP67","gene_name":"ribosomal protein SA pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:51918]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075111","summary":null,"start":67774591,"end":67777324,"strand":-1,"description":"ribosomal protein SA pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:51918]"}, {"versioned_ensembl_gene_id":"ENSG00000250946.2","gene_symbol":"AP004833.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89820082,"end":89826922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179456.10","gene_symbol":"ZBTB18","gene_name":"zinc finger and BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:13030]","synonyms":"ZNF238,TAZ-1,RP58,C2H2-171","biotype":"protein_coding","ncbi_id":"10472","summary":"This gene encodes a C2H2-type zinc finger protein which acts a transcriptional repressor of genes involved in neuronal development. The encoded protein recognizes a specific sequence motif and recruits components of chromatin to target genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":244048939,"end":244057476,"strand":1,"description":"zinc finger and BTB domain containing 18 [Source:HGNC Symbol;Acc:HGNC:13030]"}, {"versioned_ensembl_gene_id":"ENSG00000100628.11","gene_symbol":"ASB2","gene_name":"ankyrin repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:16012]","synonyms":"ASB-2","biotype":"protein_coding","ncbi_id":"51676","summary":"This gene encodes a member of the ankyrin repeat and SOCS box-containing (ASB) protein family. These proteins play a role in protein degradation by coupling suppressor of cytokine signalling (SOCS) proteins with the elongin BC complex. The encoded protein is a subunit of a multimeric E3 ubiquitin ligase complex that mediates the degradation of actin-binding proteins. This gene plays a role in retinoic acid-induced growth inhibition and differentiation of myeloid leukemia cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":93934153,"end":93976791,"strand":-1,"description":"ankyrin repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:16012]"}, {"versioned_ensembl_gene_id":"ENSG00000137494.13","gene_symbol":"ANKRD42","gene_name":"ankyrin repeat domain 42 [Source:HGNC Symbol;Acc:HGNC:26752]","synonyms":"SARP,PPP1R79,FLJ37874","biotype":"protein_coding","ncbi_id":"338699","summary":null,"start":83193739,"end":83260694,"strand":1,"description":"ankyrin repeat domain 42 [Source:HGNC Symbol;Acc:HGNC:26752]"}, {"versioned_ensembl_gene_id":"ENSG00000241020.1","gene_symbol":"AP000873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83213005,"end":83213404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167202.11","gene_symbol":"TBC1D2B","gene_name":"TBC1 domain family member 2B [Source:HGNC Symbol;Acc:HGNC:29183]","synonyms":"KIAA1055","biotype":"protein_coding","ncbi_id":"23102","summary":null,"start":77984036,"end":78077724,"strand":-1,"description":"TBC1 domain family member 2B [Source:HGNC Symbol;Acc:HGNC:29183]"}, {"versioned_ensembl_gene_id":"ENSG00000131979.18","gene_symbol":"GCH1","gene_name":"GTP cyclohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:4193]","synonyms":"DYT5,DYT14,GTPCH1,GCH,DYT5a","biotype":"protein_coding","ncbi_id":"2643","summary":"This gene encodes a member of the GTP cyclohydrolase family. The encoded protein is the first and rate-limiting enzyme in tetrahydrobiopterin (BH4) biosynthesis, catalyzing the conversion of GTP into 7,8-dihydroneopterin triphosphate. BH4 is an essential cofactor required by aromatic amino acid hydroxylases as well as nitric oxide synthases. Mutations in this gene are associated with malignant hyperphenylalaninemia and dopa-responsive dystonia. Several alternatively spliced transcript variants encoding different isoforms have been described; however, not all variants give rise to a functional enzyme. [provided by RefSeq, Jul 2008]","start":54842008,"end":54902852,"strand":-1,"description":"GTP cyclohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:4193]"}, {"versioned_ensembl_gene_id":"ENSG00000130935.9","gene_symbol":"NOL11","gene_name":"nucleolar protein 11 [Source:HGNC Symbol;Acc:HGNC:24557]","synonyms":"DKFZP586L0724","biotype":"protein_coding","ncbi_id":"25926","summary":null,"start":67717833,"end":67744531,"strand":1,"description":"nucleolar protein 11 [Source:HGNC Symbol;Acc:HGNC:24557]"}, {"versioned_ensembl_gene_id":"ENSG00000247228.2","gene_symbol":"AC009060.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70156340,"end":70173448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147162.13","gene_symbol":"OGT","gene_name":"O-linked N-acetylglucosamine (GlcNAc) transferase [Source:HGNC Symbol;Acc:HGNC:8127]","synonyms":"OGT1,O-GLCNAC,MGC22921,HRNT1,FLJ23071","biotype":"protein_coding","ncbi_id":"8473","summary":"This gene encodes a glycosyltransferase that catalyzes the addition of a single N-acetylglucosamine in O-glycosidic linkage to serine or threonine residues. Since both phosphorylation and glycosylation compete for similar serine or threonine residues, the two processes may compete for sites, or they may alter the substrate specificity of nearby sites by steric or electrostatic effects. The protein contains multiple tetratricopeptide repeats that are required for optimal recognition of substrates. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":71533083,"end":71575897,"strand":1,"description":"O-linked N-acetylglucosamine (GlcNAc) transferase [Source:HGNC Symbol;Acc:HGNC:8127]"}, {"versioned_ensembl_gene_id":"ENSG00000154721.14","gene_symbol":"JAM2","gene_name":"junctional adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:14686]","synonyms":"VE-JAM,JAMB,JAM-B,CD322,C21orf43","biotype":"protein_coding","ncbi_id":"58494","summary":"This gene belongs to the immunoglobulin superfamily, and the junctional adhesion molecule (JAM) family. The protein encoded by this gene is a type I membrane protein that is localized at the tight junctions of both epithelial and endothelial cells. It acts as an adhesive ligand for interacting with a variety of immune cell types, and may play a role in lymphocyte homing to secondary lymphoid organs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2012]","start":25639272,"end":25717562,"strand":1,"description":"junctional adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:14686]"}, {"versioned_ensembl_gene_id":"ENSG00000260089.2","gene_symbol":"ADAM3B","gene_name":"ADAM metallopeptidase domain 3B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:210]","synonyms":"CYRN2","biotype":"processed_pseudogene","ncbi_id":"1596","summary":null,"start":49517762,"end":49518601,"strand":-1,"description":"ADAM metallopeptidase domain 3B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:210]"}, {"versioned_ensembl_gene_id":"ENSG00000113048.16","gene_symbol":"MRPS27","gene_name":"mitochondrial ribosomal protein S27 [Source:HGNC Symbol;Acc:HGNC:14512]","synonyms":"KIAA0264","biotype":"protein_coding","ncbi_id":"23107","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that may be a functional partner of the death associated protein 3 (DAP3). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2013]","start":72219409,"end":72320646,"strand":-1,"description":"mitochondrial ribosomal protein S27 [Source:HGNC Symbol;Acc:HGNC:14512]"}, {"versioned_ensembl_gene_id":"ENSG00000234852.2","gene_symbol":"ZBTB12","gene_name":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]","synonyms":"C6orf46,NG35,G10,D6S59E","biotype":"protein_coding","ncbi_id":"221527","summary":null,"start":31881788,"end":31884173,"strand":-1,"description":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]"}, {"versioned_ensembl_gene_id":"ENSG00000257207.5","gene_symbol":"AC112229.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":110402934,"end":110473075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261623.1","gene_symbol":"LINC02179","gene_name":"long intergenic non-protein coding RNA 2179 [Source:HGNC Symbol;Acc:HGNC:53041]","synonyms":"RP11-189E14.4","biotype":"lincRNA","ncbi_id":"101927228","summary":null,"start":49466106,"end":49469875,"strand":1,"description":"long intergenic non-protein coding RNA 2179 [Source:HGNC Symbol;Acc:HGNC:53041]"}, {"versioned_ensembl_gene_id":"ENSG00000065534.18","gene_symbol":"MYLK","gene_name":"myosin light chain kinase [Source:HGNC Symbol;Acc:HGNC:7590]","synonyms":"smMLCK,MYLK1,MLCK1,MLCK","biotype":"protein_coding","ncbi_id":"4638","summary":"This gene, a muscle member of the immunoglobulin gene superfamily, encodes myosin light chain kinase which is a calcium/calmodulin dependent enzyme. This kinase phosphorylates myosin regulatory light chains to facilitate myosin interaction with actin filaments to produce contractile activity. This gene encodes both smooth muscle and nonmuscle isoforms. In addition, using a separate promoter in an intron in the 3' region, it encodes telokin, a small protein identical in sequence to the C-terminus of myosin light chain kinase, that is independently expressed in smooth muscle and functions to stabilize unphosphorylated myosin filaments. A pseudogene is located on the p arm of chromosome 3. Four transcript variants that produce four isoforms of the calcium/calmodulin dependent enzyme have been identified as well as two transcripts that produce two isoforms of telokin. Additional variants have been identified but lack full length transcripts. [provided by RefSeq, Jul 2008]","start":123610049,"end":123884331,"strand":-1,"description":"myosin light chain kinase [Source:HGNC Symbol;Acc:HGNC:7590]"}, {"versioned_ensembl_gene_id":"ENSG00000226576.1","gene_symbol":"AC060234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48984564,"end":49018897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230596.3","gene_symbol":"GPAA1P2","gene_name":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51484]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106481722","summary":null,"start":110386377,"end":110388163,"strand":-1,"description":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51484]"}, {"versioned_ensembl_gene_id":"ENSG00000060303.5","gene_symbol":"RPS17P5","gene_name":"ribosomal protein S17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:21352]","synonyms":"RPS17L4,dJ753D5.2","biotype":"processed_pseudogene","ncbi_id":"442216","summary":null,"start":50857255,"end":50857662,"strand":-1,"description":"ribosomal protein S17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:21352]"}, {"versioned_ensembl_gene_id":"ENSG00000169718.17","gene_symbol":"DUS1L","gene_name":"dihydrouridine synthase 1 like [Source:HGNC Symbol;Acc:HGNC:30086]","synonyms":"PP3111,DUS1","biotype":"protein_coding","ncbi_id":"64118","summary":null,"start":82057506,"end":82065887,"strand":-1,"description":"dihydrouridine synthase 1 like [Source:HGNC Symbol;Acc:HGNC:30086]"}, {"versioned_ensembl_gene_id":"ENSG00000154217.14","gene_symbol":"PITPNC1","gene_name":"phosphatidylinositol transfer protein, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:21045]","synonyms":"RDGBB1,RDGBB,RDGB-BETA","biotype":"protein_coding","ncbi_id":"26207","summary":"This gene encodes a member of the phosphatidylinositol transfer protein family. The encoded cytoplasmic protein plays a role in multiple processes including cell signaling and lipid metabolism by facilitating the transfer of phosphatidylinositol between membrane compartments. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, May 2012]","start":67377281,"end":67697261,"strand":1,"description":"phosphatidylinositol transfer protein, cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:21045]"}, {"versioned_ensembl_gene_id":"ENSG00000213785.3","gene_symbol":"AKR1B1P3","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:422]","synonyms":"ALDRL3","biotype":"processed_pseudogene","ncbi_id":"729347","summary":null,"start":16484084,"end":16484671,"strand":-1,"description":"aldo-keto reductase family 1 member B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:422]"}, {"versioned_ensembl_gene_id":"ENSG00000254878.1","gene_symbol":"AC103794.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16023190,"end":16031515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149308.16","gene_symbol":"NPAT","gene_name":"nuclear protein, coactivator of histone transcription [Source:HGNC Symbol;Acc:HGNC:7896]","synonyms":"p220,E14","biotype":"protein_coding","ncbi_id":"4863","summary":null,"start":108157215,"end":108222642,"strand":-1,"description":"nuclear protein, coactivator of histone transcription [Source:HGNC Symbol;Acc:HGNC:7896]"}, {"versioned_ensembl_gene_id":"ENSG00000249353.2","gene_symbol":"NPM1P27","gene_name":"nucleophosmin 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:45206]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422243","summary":null,"start":93682838,"end":93683667,"strand":-1,"description":"nucleophosmin 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:45206]"}, {"versioned_ensembl_gene_id":"ENSG00000165633.12","gene_symbol":"VSTM4","gene_name":"V-set and transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26470]","synonyms":"FLJ31737,C10orf72","biotype":"protein_coding","ncbi_id":"196740","summary":null,"start":49014245,"end":49115509,"strand":-1,"description":"V-set and transmembrane domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26470]"}, {"versioned_ensembl_gene_id":"ENSG00000120008.15","gene_symbol":"WDR11","gene_name":"WD repeat domain 11 [Source:HGNC Symbol;Acc:HGNC:13831]","synonyms":"WDR15,SRI1,KIAA1351,HH14,FLJ10506,DR11,BRWD2","biotype":"protein_coding","ncbi_id":"55717","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is located in the chromosome 10q25-26 region, which is frequently deleted in gliomas and tumors of other tissues, and is disrupted by the t(10;19) translocation rearrangement in glioblastoma cells. The gene location suggests that it is a candidate gene for the tumor suppressor locus. [provided by RefSeq, Jul 2008]","start":120851175,"end":120909524,"strand":1,"description":"WD repeat domain 11 [Source:HGNC Symbol;Acc:HGNC:13831]"}, {"versioned_ensembl_gene_id":"ENSG00000146826.16","gene_symbol":"C7orf43","gene_name":"chromosome 7 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:25604]","synonyms":"FLJ10925","biotype":"protein_coding","ncbi_id":"55262","summary":null,"start":100154420,"end":100158715,"strand":-1,"description":"chromosome 7 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:25604]"}, {"versioned_ensembl_gene_id":"ENSG00000264697.1","gene_symbol":"AC067819.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68527970,"end":68528123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090857.13","gene_symbol":"PDPR","gene_name":"pyruvate dehydrogenase phosphatase regulatory subunit [Source:HGNC Symbol;Acc:HGNC:30264]","synonyms":"PDP3","biotype":"protein_coding","ncbi_id":"55066","summary":"Pyruvate dehydrogenase complex (PDC) catalyzes the oxidative decarboxylation of pyruvate and links glycolysis to the tricarboxylic acid cycle and fatty acid synthesis. The dephosphorylation and reactivation of PDC is catalyzed by pyruvate dehydrogenase phosphatase (PDP). The dimeric PDP has a catalytic subunit and a regulatory subunit. This gene encodes the FAD-containing regulatory subunit of PDP. The encoded protein acts to decrease the sensitivity of the PDP catalytic subunit to magnesium ions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]","start":70113626,"end":70162537,"strand":1,"description":"pyruvate dehydrogenase phosphatase regulatory subunit [Source:HGNC Symbol;Acc:HGNC:30264]"}, {"versioned_ensembl_gene_id":"ENSG00000253797.2","gene_symbol":"UTP14C","gene_name":"UTP14C, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:20321]","synonyms":"KIAA0266,2700066J21Rik","biotype":"protein_coding","ncbi_id":"9724","summary":null,"start":52024691,"end":52033600,"strand":1,"description":"UTP14C, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:20321]"}, {"versioned_ensembl_gene_id":"ENSG00000263567.1","gene_symbol":"AC007923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31762440,"end":31769048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110693.17","gene_symbol":"SOX6","gene_name":"SRY-box 6 [Source:HGNC Symbol;Acc:HGNC:16421]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55553","summary":"This gene encodes a member of the D subfamily of sex determining region y-related transcription factors that are characterized by a conserved DNA-binding domain termed the high mobility group box and by their ability to bind the minor groove of DNA. The encoded protein is a transcriptional activator that is required for normal development of the central nervous system, chondrogenesis and maintenance of cardiac and skeletal muscle cells. The encoded protein interacts with other family members to cooperatively activate gene expression. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]","start":15966449,"end":16739591,"strand":-1,"description":"SRY-box 6 [Source:HGNC Symbol;Acc:HGNC:16421]"}, {"versioned_ensembl_gene_id":"ENSG00000266448.1","gene_symbol":"AC007923.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31709568,"end":31709859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138698.14","gene_symbol":"RAP1GDS1","gene_name":"Rap1 GTPase-GDP dissociation stimulator 1 [Source:HGNC Symbol;Acc:HGNC:9859]","synonyms":"SmgGDS","biotype":"protein_coding","ncbi_id":"5910","summary":"The smg GDP dissociation stimulator (smgGDS) protein is a stimulatory GDP/GTP exchange protein with GTPase activity (Riess et al., 1993 [PubMed 8262526]).[supplied by OMIM, Feb 2010]","start":98261384,"end":98443861,"strand":1,"description":"Rap1 GTPase-GDP dissociation stimulator 1 [Source:HGNC Symbol;Acc:HGNC:9859]"}, {"versioned_ensembl_gene_id":"ENSG00000264869.1","gene_symbol":"AC068112.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68102116,"end":68114377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233006.6","gene_symbol":"MIR3936HG","gene_name":"MIR3936 host gene [Source:HGNC Symbol;Acc:HGNC:40538]","synonyms":"SLC22A5-AS1,LOC553103","biotype":"processed_transcript","ncbi_id":"553103","summary":null,"start":132311285,"end":132369916,"strand":-1,"description":"MIR3936 host gene [Source:HGNC Symbol;Acc:HGNC:40538]"}, {"versioned_ensembl_gene_id":"ENSG00000229831.2","gene_symbol":"AC108039.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61820208,"end":61820566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116584.17","gene_symbol":"ARHGEF2","gene_name":"Rho/Rac guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:682]","synonyms":"P40,LFP40,KIAA0651,GEF-H1","biotype":"protein_coding","ncbi_id":"9181","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form complex with G proteins and stimulate rho-dependent signals. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Jun 2009]","start":155946851,"end":156007070,"strand":-1,"description":"Rho/Rac guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:682]"}, {"versioned_ensembl_gene_id":"ENSG00000253710.2","gene_symbol":"ALG11","gene_name":"ALG11, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:32456]","synonyms":"KIAA0266,CDG1P","biotype":"protein_coding","ncbi_id":"440138","summary":"This gene encodes a GDP-Man:Man3GlcNAc2-PP-dolichol-alpha1,2-mannosyltransferase which is localized to the cytosolic side of the endoplasmic reticulum (ER) and catalyzes the transfer of the fourth and fifth mannose residue from GDP-mannose (GDP-Man) to Man3GlcNAc2-PP-dolichol and Man4GlcNAc2-PP-dolichol resulting in the production of Man5GlcNAc2-PP-dolichol. Mutations in this gene are associated with congenital disorder of glycosylation type Ip (CDGIP). This gene overlaps but is distinct from the UTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast) gene. A pseudogene of the GDP-Man:Man3GlcNAc2-PP-dolichol-alpha1,2-mannosyltransferase has been identified on chromosome 19. [provided by RefSeq, Aug 2010]","start":52012398,"end":52029664,"strand":1,"description":"ALG11, alpha-1,2-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:32456]"}, {"versioned_ensembl_gene_id":"ENSG00000278546.1","gene_symbol":"AC003101.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31560132,"end":31560573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227361.1","gene_symbol":"RPS24P7","gene_name":"ribosomal protein S24 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216342","summary":null,"start":61803143,"end":61803388,"strand":1,"description":"ribosomal protein S24 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35737]"}, {"versioned_ensembl_gene_id":"ENSG00000224276.1","gene_symbol":"AL355388.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155991390,"end":156001787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251142.1","gene_symbol":"AC025674.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57240057,"end":57240541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237714.1","gene_symbol":"P4HA2-AS1","gene_name":"P4HA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43560]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861518","summary":null,"start":132184876,"end":132192808,"strand":1,"description":"P4HA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43560]"}, {"versioned_ensembl_gene_id":"ENSG00000253301.5","gene_symbol":"LINC01606","gene_name":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]","synonyms":"TCONS_l2_00027778","biotype":"lincRNA","ncbi_id":"100507651","summary":null,"start":57142689,"end":57240298,"strand":1,"description":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]"}, {"versioned_ensembl_gene_id":"ENSG00000233999.3","gene_symbol":"IGKV3OR2-268","gene_name":"immunoglobulin kappa variable 3/OR2-268 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5830]","synonyms":"IGKV3OR2-268A,IGKV3/OR2-268A,IGKV3/OR2-268,IGKV268","biotype":"IG_V_gene","ncbi_id":"3523","summary":null,"start":87338511,"end":87339035,"strand":1,"description":"immunoglobulin kappa variable 3/OR2-268 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5830]"}, {"versioned_ensembl_gene_id":"ENSG00000271097.1","gene_symbol":"AC083899.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87301658,"end":87302251,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263110.1","gene_symbol":"AC007861.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49454229,"end":49457269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233706.1","gene_symbol":"AL353689.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":226992140,"end":226993206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121904.17","gene_symbol":"CSMD2","gene_name":"CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:HGNC:19290]","synonyms":"KIAA1884","biotype":"protein_coding","ncbi_id":"114784","summary":"The protein encoded by this gene is thought to be involved in the control of complement cascade of the immune system. Defects in this gene have been associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided by RefSeq, Jan 2020]","start":33513999,"end":34165842,"strand":-1,"description":"CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:HGNC:19290]"}, {"versioned_ensembl_gene_id":"ENSG00000110696.9","gene_symbol":"C11orf58","gene_name":"chromosome 11 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:16990]","synonyms":"SMAP","biotype":"protein_coding","ncbi_id":"10944","summary":null,"start":16613132,"end":16756881,"strand":1,"description":"chromosome 11 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:16990]"}, {"versioned_ensembl_gene_id":"ENSG00000277773.4","gene_symbol":"SMN2","gene_name":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]","synonyms":"GEMIN1,BCD541,TDRD16B,SMNC","biotype":"protein_coding","ncbi_id":"6607","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Sep 2008]","start":69673667,"end":69702549,"strand":-1,"description":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]"}, {"versioned_ensembl_gene_id":"ENSG00000226085.3","gene_symbol":"UQCRFS1P1","gene_name":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12588]","synonyms":"UQCRFSL1","biotype":"processed_pseudogene","ncbi_id":"100128525","summary":null,"start":39875289,"end":39876108,"strand":1,"description":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12588]"}, {"versioned_ensembl_gene_id":"ENSG00000224927.2","gene_symbol":"NDUFA5P10","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724853","summary":null,"start":109810642,"end":109810998,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48852]"}, {"versioned_ensembl_gene_id":"ENSG00000266922.1","gene_symbol":"AC008543.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11725961,"end":11730783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248664.1","gene_symbol":"AC010273.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69113112,"end":69136394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265097.1","gene_symbol":"RBM22P1","gene_name":"RNA binding motif protein 22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31466]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400645","summary":null,"start":27418884,"end":27420435,"strand":-1,"description":"RNA binding motif protein 22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31466]"}, {"versioned_ensembl_gene_id":"ENSG00000244329.1","gene_symbol":"AC021382.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27355406,"end":27355764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132467.3","gene_symbol":"UTP3","gene_name":"UTP3, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24477]","synonyms":"SAS10,FLJ23256,DKFZp761F222,CRLZ1","biotype":"protein_coding","ncbi_id":"57050","summary":null,"start":70688479,"end":70690551,"strand":1,"description":"UTP3, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24477]"}, {"versioned_ensembl_gene_id":"ENSG00000176531.10","gene_symbol":"PHLDB3","gene_name":"pleckstrin homology like domain family B member 3 [Source:HGNC Symbol;Acc:HGNC:30499]","synonyms":"FLJ40193","biotype":"protein_coding","ncbi_id":"653583","summary":null,"start":43474954,"end":43504935,"strand":-1,"description":"pleckstrin homology like domain family B member 3 [Source:HGNC Symbol;Acc:HGNC:30499]"}, {"versioned_ensembl_gene_id":"ENSG00000166736.11","gene_symbol":"HTR3A","gene_name":"5-hydroxytryptamine receptor 3A [Source:HGNC Symbol;Acc:HGNC:5297]","synonyms":"HTR3,5-HT3R,5-HT3A","biotype":"protein_coding","ncbi_id":"3359","summary":"The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit A of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor causes fast, depolarizing responses in neurons after activation. It appears that the heteromeric combination of A and B subunits is necessary to provide the full functional features of this receptor, since either subunit alone results in receptors with very low conductance and response amplitude. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":113974881,"end":113990313,"strand":1,"description":"5-hydroxytryptamine receptor 3A [Source:HGNC Symbol;Acc:HGNC:5297]"}, {"versioned_ensembl_gene_id":"ENSG00000149311.18","gene_symbol":"ATM","gene_name":"ATM serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:795]","synonyms":"TELO1,TEL1,ATDC,ATD,ATC,ATA","biotype":"protein_coding","ncbi_id":"472","summary":"The protein encoded by this gene belongs to the PI3/PI4-kinase family. This protein is an important cell cycle checkpoint kinase that phosphorylates; thus, it functions as a regulator of a wide variety of downstream proteins, including tumor suppressor proteins p53 and BRCA1, checkpoint kinase CHK2, checkpoint proteins RAD17 and RAD9, and DNA repair protein NBS1. This protein and the closely related kinase ATR are thought to be master controllers of cell cycle checkpoint signaling pathways that are required for cell response to DNA damage and for genome stability. Mutations in this gene are associated with ataxia telangiectasia, an autosomal recessive disorder. [provided by RefSeq, Aug 2010]","start":108222484,"end":108369102,"strand":1,"description":"ATM serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:795]"}, {"versioned_ensembl_gene_id":"ENSG00000226744.1","gene_symbol":"AC005326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97870167,"end":97870289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232097.1","gene_symbol":"AC079781.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97938439,"end":97938794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243554.1","gene_symbol":"AC004967.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97969005,"end":97972254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240568.1","gene_symbol":"AC107626.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68192398,"end":68192580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231812.1","gene_symbol":"SNRPCP9","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49824]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310853","summary":null,"start":97885868,"end":97886074,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49824]"}, {"versioned_ensembl_gene_id":"ENSG00000224075.1","gene_symbol":"TTTY22","gene_name":"testis-specific transcript, Y-linked 22 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18846]","synonyms":"NCRNA00147","biotype":"lincRNA","ncbi_id":"252954","summary":null,"start":9801153,"end":9813245,"strand":1,"description":"testis-specific transcript, Y-linked 22 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18846]"}, {"versioned_ensembl_gene_id":"ENSG00000284707.1","gene_symbol":"AC079781.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":97851688,"end":97972985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197375.12","gene_symbol":"SLC22A5","gene_name":"solute carrier family 22 member 5 [Source:HGNC Symbol;Acc:HGNC:10969]","synonyms":"SCD,OCTN2,CDSP","biotype":"protein_coding","ncbi_id":"6584","summary":"Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":132369752,"end":132395614,"strand":1,"description":"solute carrier family 22 member 5 [Source:HGNC Symbol;Acc:HGNC:10969]"}, {"versioned_ensembl_gene_id":"ENSG00000284627.1","gene_symbol":"AC079781.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97928082,"end":97928300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282326.1","gene_symbol":"TRBV12-2","gene_name":"T-cell receptor beta variable 12-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12184]","synonyms":"TRBV122,TCRBV8S5P,TCRBV12S2","biotype":"TR_V_pseudogene","ncbi_id":"28578","summary":null,"start":142462583,"end":142463025,"strand":1,"description":"T-cell receptor beta variable 12-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12184]"}, {"versioned_ensembl_gene_id":"ENSG00000213908.4","gene_symbol":"CYP2A7P1","gene_name":"cytochrome P450 family 2 subfamily A member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2612]","synonyms":"CYP2A7PT,CYP2A18PN","biotype":"unprocessed_pseudogene","ncbi_id":"1550","summary":null,"start":41024268,"end":41027720,"strand":-1,"description":"cytochrome P450 family 2 subfamily A member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2612]"}, {"versioned_ensembl_gene_id":"ENSG00000233826.1","gene_symbol":"BX119924.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28838582,"end":28839719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219881.1","gene_symbol":"GAPDHP42","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:37799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240707","summary":null,"start":69745871,"end":69746851,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:37799]"}, {"versioned_ensembl_gene_id":"ENSG00000183662.10","gene_symbol":"FAM19A1","gene_name":"family with sequence similarity 19 member A1, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21587]","synonyms":"TAFA1,TAFA-1","biotype":"protein_coding","ncbi_id":"407738","summary":"This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines that act as regulators of immune and nervous cells. [provided by RefSeq, Jul 2008]","start":68004216,"end":68545625,"strand":1,"description":"family with sequence similarity 19 member A1, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21587]"}, {"versioned_ensembl_gene_id":"ENSG00000203907.9","gene_symbol":"OOEP","gene_name":"oocyte expressed protein [Source:HGNC Symbol;Acc:HGNC:21382]","synonyms":"C6orf156,KHDC2,Em:AC019205.2","biotype":"protein_coding","ncbi_id":"441161","summary":null,"start":73368555,"end":73395133,"strand":-1,"description":"oocyte expressed protein [Source:HGNC Symbol;Acc:HGNC:21382]"}, {"versioned_ensembl_gene_id":"ENSG00000265656.1","gene_symbol":"AC106037.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21673628,"end":21682561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198265.11","gene_symbol":"HELZ","gene_name":"helicase with zinc finger [Source:HGNC Symbol;Acc:HGNC:16878]","synonyms":"DHRC,KIAA0054,HUMORF5","biotype":"protein_coding","ncbi_id":"9931","summary":"HELZ is a member of the superfamily I class of RNA helicases. RNA helicases alter the conformation of RNA by unwinding double-stranded regions, thereby altering the biologic activity of the RNA molecule and regulating access to other proteins (Wagner et al., 1999 [PubMed 10471385]).[supplied by OMIM, Mar 2008]","start":67070438,"end":67245989,"strand":-1,"description":"helicase with zinc finger [Source:HGNC Symbol;Acc:HGNC:16878]"}, {"versioned_ensembl_gene_id":"ENSG00000222019.7","gene_symbol":"URAHP","gene_name":"urate (hydroxyiso-) hydrolase, pseudogene [Source:HGNC Symbol;Acc:HGNC:43695]","synonyms":"URAH","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100130015","summary":null,"start":90039761,"end":90047773,"strand":-1,"description":"urate (hydroxyiso-) hydrolase, pseudogene [Source:HGNC Symbol;Acc:HGNC:43695]"}, {"versioned_ensembl_gene_id":"ENSG00000266473.1","gene_symbol":"AC007448.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67244837,"end":67245806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197332.8","gene_symbol":"AC008543.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11639776,"end":11686569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275009.2","gene_symbol":"GOLGA6L1","gene_name":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283767","summary":null,"start":23131736,"end":23140290,"strand":-1,"description":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]"}, {"versioned_ensembl_gene_id":"ENSG00000274272.1","gene_symbol":"AC069281.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":100572232,"end":100578700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244040.5","gene_symbol":"IL12A-AS1","gene_name":"IL12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49094]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928376","summary":null,"start":159913400,"end":160225299,"strand":-1,"description":"IL12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49094]"}, {"versioned_ensembl_gene_id":"ENSG00000229433.1","gene_symbol":"LINC02069","gene_name":"long intergenic non-protein coding RNA 2069 [Source:HGNC Symbol;Acc:HGNC:52915]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928992","summary":null,"start":184756389,"end":184773155,"strand":-1,"description":"long intergenic non-protein coding RNA 2069 [Source:HGNC Symbol;Acc:HGNC:52915]"}, {"versioned_ensembl_gene_id":"ENSG00000272970.1","gene_symbol":"AC107294.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184734075,"end":184738949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089505.17","gene_symbol":"CMTM1","gene_name":"CKLF like MARVEL transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19172]","synonyms":"CKLFSF1,CKLFH1a,CKLFH","biotype":"protein_coding","ncbi_id":"113540","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. The protein encoded by this gene may play an important role in testicular development. Alternatively spliced transcript variants encoding different isoforms have been identified. Naturally occurring read-through transcription occurs between this locus and the neighboring locus CKLF (chemokine-like factor).[provided by RefSeq, Feb 2011]","start":66566393,"end":66579137,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19172]"}, {"versioned_ensembl_gene_id":"ENSG00000241316.6","gene_symbol":"SUCLG2-AS1","gene_name":"SUCLG2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49643]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927111","summary":null,"start":67654697,"end":67947713,"strand":1,"description":"SUCLG2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49643]"}, {"versioned_ensembl_gene_id":"ENSG00000282436.1","gene_symbol":"TRBV11-2","gene_name":"T-cell receptor beta variable 11-2 [Source:HGNC Symbol;Acc:HGNC:12181]","synonyms":"TRBV112,TCRBV21S3A2N2T,TCRBV11S2","biotype":"lincRNA","ncbi_id":"28581","summary":null,"start":142455594,"end":142456093,"strand":1,"description":"T-cell receptor beta variable 11-2 [Source:HGNC Symbol;Acc:HGNC:12181]"}, {"versioned_ensembl_gene_id":"ENSG00000142973.13","gene_symbol":"CYP4B1","gene_name":"cytochrome P450 family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2644]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1580","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. In rodents, the homologous protein has been shown to metabolize certain carcinogens; however, the specific function of the human protein has not been determined. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":46757838,"end":46819413,"strand":1,"description":"cytochrome P450 family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2644]"}, {"versioned_ensembl_gene_id":"ENSG00000003249.13","gene_symbol":"DBNDD1","gene_name":"dysbindin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28455]","synonyms":"MGC3101,FLJ12582","biotype":"protein_coding","ncbi_id":"79007","summary":null,"start":90004865,"end":90020128,"strand":-1,"description":"dysbindin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28455]"}, {"versioned_ensembl_gene_id":"ENSG00000243896.4","gene_symbol":"OR2A7","gene_name":"olfactory receptor family 2 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:8234]","synonyms":"HSDJ0798C17","biotype":"protein_coding","ncbi_id":"401427","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144257663,"end":144264792,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:8234]"}, {"versioned_ensembl_gene_id":"ENSG00000232871.8","gene_symbol":"SEC1P","gene_name":"secretory blood group 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:44149]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"653677","summary":null,"start":48638071,"end":48682245,"strand":1,"description":"secretory blood group 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:44149]"}, {"versioned_ensembl_gene_id":"ENSG00000254429.1","gene_symbol":"AP001972.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75260127,"end":75261025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264054.1","gene_symbol":"AC113195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67137611,"end":67137751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163807.5","gene_symbol":"KIAA1143","gene_name":"KIAA1143 [Source:HGNC Symbol;Acc:HGNC:29198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57456","summary":null,"start":44737661,"end":44761662,"strand":-1,"description":"KIAA1143 [Source:HGNC Symbol;Acc:HGNC:29198]"}, {"versioned_ensembl_gene_id":"ENSG00000020577.13","gene_symbol":"SAMD4A","gene_name":"sterile alpha motif domain containing 4A [Source:HGNC Symbol;Acc:HGNC:23023]","synonyms":"SMG,Smaug,SAMD4,KIAA1053,hSmaug1,DKFZP434H0350,SMGA","biotype":"protein_coding","ncbi_id":"23034","summary":"Sterile alpha motifs (SAMs) in proteins such as SAMD4A are part of an RNA-binding domain that functions as a posttranscriptional regulator by binding to an RNA sequence motif known as the Smaug recognition element, which was named after the Drosophila Smaug protein (Baez and Boccaccio, 2005 [PubMed 16221671]).[supplied by OMIM, Mar 2008]","start":54567097,"end":54793315,"strand":1,"description":"sterile alpha motif domain containing 4A [Source:HGNC Symbol;Acc:HGNC:23023]"}, {"versioned_ensembl_gene_id":"ENSG00000110675.12","gene_symbol":"ELMOD1","gene_name":"ELMO domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25334]","synonyms":"DKFZp547C176","biotype":"protein_coding","ncbi_id":"55531","summary":null,"start":107591091,"end":107666779,"strand":1,"description":"ELMO domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25334]"}, {"versioned_ensembl_gene_id":"ENSG00000261003.1","gene_symbol":"AL008628.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":170414139,"end":170419325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263520.1","gene_symbol":"LINC02563","gene_name":"long intergenic non-protein coding RNA 2563 [Source:HGNC Symbol;Acc:HGNC:52923]","synonyms":"CRAT40","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65457541,"end":65458408,"strand":1,"description":"long intergenic non-protein coding RNA 2563 [Source:HGNC Symbol;Acc:HGNC:52923]"}, {"versioned_ensembl_gene_id":"ENSG00000131351.14","gene_symbol":"HAUS8","gene_name":"HAUS augmin like complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:30532]","synonyms":"MGC20533,HICE1,NY-SAR-48","biotype":"protein_coding","ncbi_id":"93323","summary":"HAUS8 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]","start":17049729,"end":17075625,"strand":-1,"description":"HAUS augmin like complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:30532]"}, {"versioned_ensembl_gene_id":"ENSG00000254438.1","gene_symbol":"AC022240.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13921450,"end":13924863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265351.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32328397,"end":32328503,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000240403.5","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"cl-5,nkat4b,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850443,"end":54867207,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000250930.5","gene_symbol":"LNX1-AS1","gene_name":"LNX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40345]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873939","summary":null,"start":53496400,"end":53549578,"strand":1,"description":"LNX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40345]"}, {"versioned_ensembl_gene_id":"ENSG00000228021.7","gene_symbol":"AL158835.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":125683229,"end":125709677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259907.1","gene_symbol":"AC004817.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71181456,"end":71182106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119682.16","gene_symbol":"AREL1","gene_name":"apoptosis resistant E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:20363]","synonyms":"KIAA0317,FIEL1","biotype":"protein_coding","ncbi_id":"9870","summary":null,"start":74653437,"end":74713115,"strand":-1,"description":"apoptosis resistant E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:20363]"}, {"versioned_ensembl_gene_id":"ENSG00000154188.9","gene_symbol":"ANGPT1","gene_name":"angiopoietin 1 [Source:HGNC Symbol;Acc:HGNC:484]","synonyms":"KIAA0003,Ang1","biotype":"protein_coding","ncbi_id":"284","summary":"This gene encodes a secreted glycoprotein that belongs to the angiopoietin family. Members of this family play important roles in vascular development and angiogenesis. All angiopoietins bind with similar affinity to an endothelial cell-specific tyrosine-protein kinase receptor. The protein encoded by this gene is a secreted glycoprotein that activates the receptor by inducing its tyrosine phosphorylation. It plays a critical role in mediating reciprocal interactions between the endothelium and surrounding matrix and mesenchyme and inhibits endothelial permeability. The protein also contributes to blood vessel maturation and stability, and may be involved in early development of the heart. Mutations in this gene are associated with hereditary angioedema. [provided by RefSeq, Aug 2020]","start":107249482,"end":107498055,"strand":-1,"description":"angiopoietin 1 [Source:HGNC Symbol;Acc:HGNC:484]"}, {"versioned_ensembl_gene_id":"ENSG00000256643.1","gene_symbol":"LINC02441","gene_name":"long intergenic non-protein coding RNA 2441 [Source:HGNC Symbol;Acc:HGNC:53373]","synonyms":"CRAT8","biotype":"lincRNA","ncbi_id":"105370070","summary":null,"start":128023788,"end":128027166,"strand":-1,"description":"long intergenic non-protein coding RNA 2441 [Source:HGNC Symbol;Acc:HGNC:53373]"}, {"versioned_ensembl_gene_id":"ENSG00000229314.5","gene_symbol":"ORM1","gene_name":"orosomucoid 1 [Source:HGNC Symbol;Acc:HGNC:8498]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5004","summary":"This gene encodes a key acute phase plasma protein. Because of its increase due to acute inflammation, this protein is classified as an acute-phase reactant. The specific function of this protein has not yet been determined; however, it may be involved in aspects of immunosuppression. [provided by RefSeq, Jul 2008]","start":114323056,"end":114326475,"strand":1,"description":"orosomucoid 1 [Source:HGNC Symbol;Acc:HGNC:8498]"}, {"versioned_ensembl_gene_id":"ENSG00000164087.7","gene_symbol":"POC1A","gene_name":"POC1 centriolar protein A [Source:HGNC Symbol;Acc:HGNC:24488]","synonyms":"WDR51A,DKFZP434C245","biotype":"protein_coding","ncbi_id":"25886","summary":"POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutations in this gene result in short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT) syndrome. [provided by RefSeq, Sep 2012]","start":52075253,"end":52154690,"strand":-1,"description":"POC1 centriolar protein A [Source:HGNC Symbol;Acc:HGNC:24488]"}, {"versioned_ensembl_gene_id":"ENSG00000256971.1","gene_symbol":"LINC00508","gene_name":"long intergenic non-protein coding RNA 508 [Source:HGNC Symbol;Acc:HGNC:43559]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104472718","summary":null,"start":127940595,"end":127950160,"strand":-1,"description":"long intergenic non-protein coding RNA 508 [Source:HGNC Symbol;Acc:HGNC:43559]"}, {"versioned_ensembl_gene_id":"ENSG00000259232.2","gene_symbol":"AC105129.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65475318,"end":65475614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256371.1","gene_symbol":"LRRC34P1","gene_name":"leucine rich repeat containing 34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49887]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288378","summary":null,"start":22573425,"end":22575105,"strand":1,"description":"leucine rich repeat containing 34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49887]"}, {"versioned_ensembl_gene_id":"ENSG00000235805.1","gene_symbol":"SOCS5P3","gene_name":"suppressor of cytokine signaling 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44599]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127945","summary":null,"start":44709311,"end":44710886,"strand":-1,"description":"suppressor of cytokine signaling 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44599]"}, {"versioned_ensembl_gene_id":"ENSG00000234376.4","gene_symbol":"UBTFL2","gene_name":"upstream binding transcription factor, RNA polymerase I-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35169]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"120126","summary":null,"start":89752785,"end":89753975,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35169]"}, {"versioned_ensembl_gene_id":"ENSG00000145725.19","gene_symbol":"PPIP5K2","gene_name":"diphosphoinositol pentakisphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:29035]","synonyms":"VIP2,KIAA0433,HISPPD1,CFAP160","biotype":"protein_coding","ncbi_id":"23262","summary":"This gene encodes a member of the histidine acid phosphatase family of proteins. Despite containing a histidine acid phosphatase domain, the encoded protein functions as an inositol pyrophosphate kinase, and is thought to lack phosphatase activity. This kinase activity is the mechanism by which the encoded protein synthesizes high-energy inositol pyrophosphates, which act as signaling molecules that regulate cellular homeostasis and other processes. This gene may be associated with autism spectrum disorder in human patients. [provided by RefSeq, Sep 2016]","start":103120149,"end":103212799,"strand":1,"description":"diphosphoinositol pentakisphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:29035]"}, {"versioned_ensembl_gene_id":"ENSG00000257074.3","gene_symbol":"RPL29P33","gene_name":"ribosomal protein L29 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401911","summary":null,"start":34296277,"end":34296592,"strand":-1,"description":"ribosomal protein L29 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36923]"}, {"versioned_ensembl_gene_id":"ENSG00000258521.1","gene_symbol":"AL157871.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100339832,"end":100340554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260009.1","gene_symbol":"LINC02130","gene_name":"long intergenic non-protein coding RNA 2130 [Source:HGNC Symbol;Acc:HGNC:52989]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105447648","summary":null,"start":14363109,"end":14370266,"strand":-1,"description":"long intergenic non-protein coding RNA 2130 [Source:HGNC Symbol;Acc:HGNC:52989]"}, {"versioned_ensembl_gene_id":"ENSG00000182264.8","gene_symbol":"IZUMO1","gene_name":"izumo sperm-egg fusion 1 [Source:HGNC Symbol;Acc:HGNC:28539]","synonyms":"OBF,MGC34799,IZUMO","biotype":"protein_coding","ncbi_id":"284359","summary":"The sperm-specific protein Izumo, named for a Japanese shrine dedicated to marriage, is essential for sperm-egg plasma membrane binding and fusion (Inoue et al., 2005 [PubMed 15759005]).[supplied by OMIM, Mar 2008]","start":48740852,"end":48746909,"strand":-1,"description":"izumo sperm-egg fusion 1 [Source:HGNC Symbol;Acc:HGNC:28539]"}, {"versioned_ensembl_gene_id":"ENSG00000259252.1","gene_symbol":"AC026583.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70195638,"end":70198509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255429.1","gene_symbol":"AP003400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89546637,"end":89589611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280191.3","gene_symbol":"LINC01669","gene_name":"long intergenic non-protein coding RNA 1669 [Source:HGNC Symbol;Acc:HGNC:52457]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724354","summary":null,"start":6060340,"end":6076305,"strand":1,"description":"long intergenic non-protein coding RNA 1669 [Source:HGNC Symbol;Acc:HGNC:52457]"}, {"versioned_ensembl_gene_id":"ENSG00000233711.1","gene_symbol":"EIF4EBP2P1","gene_name":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16596]","synonyms":"EIF4EBP2P,dJ862K6.3","biotype":"processed_pseudogene","ncbi_id":"170510","summary":null,"start":43423196,"end":43423538,"strand":-1,"description":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16596]"}, {"versioned_ensembl_gene_id":"ENSG00000170445.12","gene_symbol":"HARS","gene_name":"histidyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:4816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3035","summary":"Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is a cytoplasmic enzyme which belongs to the class II family of aminoacyl-tRNA synthetases. The enzyme is responsible for the synthesis of histidyl-transfer RNA, which is essential for the incorporation of histidine into proteins. The gene is located in a head-to-head orientation with HARSL on chromosome five, where the homologous genes share a bidirectional promoter. The gene product is a frequent target of autoantibodies in the human autoimmune disease polymyositis/dermatomyositis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":140673173,"end":140692024,"strand":-1,"description":"histidyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:4816]"}, {"versioned_ensembl_gene_id":"ENSG00000276536.4","gene_symbol":"HRAS","gene_name":"HRas proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:5173]","synonyms":"HRAS1","biotype":"protein_coding","ncbi_id":"3265","summary":"This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, cognitive disability, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":532242,"end":537287,"strand":-1,"description":"HRas proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:5173]"}, {"versioned_ensembl_gene_id":"ENSG00000225058.1","gene_symbol":"AC092941.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187997422,"end":188003990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166503.8","gene_symbol":"HDGFL3","gene_name":"HDGF like 3 [Source:HGNC Symbol;Acc:HGNC:24937]","synonyms":"HRP-3,Hdgfrp3","biotype":"protein_coding","ncbi_id":"50810","summary":null,"start":83112738,"end":83208018,"strand":-1,"description":"HDGF like 3 [Source:HGNC Symbol;Acc:HGNC:24937]"}, {"versioned_ensembl_gene_id":"ENSG00000236824.2","gene_symbol":"BCYRN1","gene_name":"brain cytoplasmic RNA 1 [Source:HGNC Symbol;Acc:HGNC:1022]","synonyms":"NCRNA00004,LINC00004,BC200a,BC200","biotype":"scRNA","ncbi_id":"618","summary":"This gene, which encodes a neural small non-messenger RNA, is a member of the family of interspersed repetitive DNA, and its product represents an example of a primate tissue-specific RNA polymerase III transcript. The RNA sequence is divided into three domains: a 5' portion homologous to the Alu Lm, a central adenosine-rich region, and the terminal 43-nt nonrepetitive domain. It is believed that this gene was retropositionally generated and recruited into a function regulating dendritic protein biosynthesis. At least two pseudogenes of this gene have been identified. [provided by RefSeq, Jul 2008]","start":47335315,"end":47335514,"strand":1,"description":"brain cytoplasmic RNA 1 [Source:HGNC Symbol;Acc:HGNC:1022]"}, {"versioned_ensembl_gene_id":"ENSG00000256286.1","gene_symbol":"AC078878.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126874821,"end":126876232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233007.1","gene_symbol":"UBTFL11","gene_name":"upstream binding transcription factor, RNA polymerase I-like 11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50288]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442446","summary":null,"start":38531923,"end":38534174,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50288]"}, {"versioned_ensembl_gene_id":"ENSG00000226899.1","gene_symbol":"AL731577.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124945204,"end":124946432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226223.1","gene_symbol":"TSPY16P","gene_name":"testis specific protein, Y-linked 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:37712]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"727969","summary":null,"start":9640249,"end":9640716,"strand":-1,"description":"testis specific protein, Y-linked 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:37712]"}, {"versioned_ensembl_gene_id":"ENSG00000214142.2","gene_symbol":"RPL7P60","gene_name":"ribosomal protein L7 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:49216]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289264","summary":null,"start":100139629,"end":100140682,"strand":-1,"description":"ribosomal protein L7 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:49216]"}, {"versioned_ensembl_gene_id":"ENSG00000254478.1","gene_symbol":"AP004609.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118821895,"end":118822084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186235.10","gene_symbol":"AC016757.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":238224552,"end":238231677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175029.16","gene_symbol":"CTBP2","gene_name":"C-terminal binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2495]","synonyms":"ribeye","biotype":"protein_coding","ncbi_id":"1488","summary":"This gene produces alternative transcripts encoding two distinct proteins. One protein is a transcriptional repressor, while the other isoform is a major component of specialized synapses known as synaptic ribbons. Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases. A portion of the 3' untranslated region was used to map this gene to chromosome 21q21.3; however, it was noted that similar loci elsewhere in the genome are likely. Blast analysis shows that this gene is present on chromosome 10. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]","start":124984317,"end":125161170,"strand":-1,"description":"C-terminal binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2495]"}, {"versioned_ensembl_gene_id":"ENSG00000143314.12","gene_symbol":"MRPL24","gene_name":"mitochondrial ribosomal protein L24 [Source:HGNC Symbol;Acc:HGNC:14037]","synonyms":"MRP-L18","biotype":"protein_coding","ncbi_id":"79590","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which is more than twice the size of its E.coli counterpart (EcoL24). Sequence analysis identified two transcript variants that encode the same protein. [provided by RefSeq, Jul 2008]","start":156737303,"end":156741590,"strand":-1,"description":"mitochondrial ribosomal protein L24 [Source:HGNC Symbol;Acc:HGNC:14037]"}, {"versioned_ensembl_gene_id":"ENSG00000254436.1","gene_symbol":"AP000648.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90098421,"end":90098817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198723.10","gene_symbol":"TEX45","gene_name":"testis expressed 45 [Source:HGNC Symbol;Acc:HGNC:24745]","synonyms":"C19orf45,FLJ35784","biotype":"protein_coding","ncbi_id":"374877","summary":null,"start":7492976,"end":7508450,"strand":1,"description":"testis expressed 45 [Source:HGNC Symbol;Acc:HGNC:24745]"}, {"versioned_ensembl_gene_id":"ENSG00000131732.11","gene_symbol":"ZCCHC9","gene_name":"zinc finger CCHC-type containing 9 [Source:HGNC Symbol;Acc:HGNC:25424]","synonyms":"PPP1R41,DKFZp761J139","biotype":"protein_coding","ncbi_id":"84240","summary":null,"start":81301590,"end":81313297,"strand":1,"description":"zinc finger CCHC-type containing 9 [Source:HGNC Symbol;Acc:HGNC:25424]"}, {"versioned_ensembl_gene_id":"ENSG00000261423.1","gene_symbol":"TMEM202-AS1","gene_name":"TMEM202 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53265]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370888","summary":null,"start":72407778,"end":72475168,"strand":-1,"description":"TMEM202 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53265]"}, {"versioned_ensembl_gene_id":"ENSG00000131626.16","gene_symbol":"PPFIA1","gene_name":"PTPRF interacting protein alpha 1 [Source:HGNC Symbol;Acc:HGNC:9245]","synonyms":"LIPRIN,LIP.1","biotype":"protein_coding","ncbi_id":"8500","summary":"The protein encoded by this gene is a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. Liprins interact with members of LAR family of transmembrane protein tyrosine phosphatases, which are known to be important for axon guidance and mammary gland development. This protein binds to the intracellular membrane-distal phosphatase domain of tyrosine phosphatase LAR, and appears to localize LAR to cell focal adhesions. This interaction may regulate the disassembly of focal adhesion and thus help orchestrate cell-matrix interactions. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":70270700,"end":70384403,"strand":1,"description":"PTPRF interacting protein alpha 1 [Source:HGNC Symbol;Acc:HGNC:9245]"}, {"versioned_ensembl_gene_id":"ENSG00000013293.5","gene_symbol":"SLC7A14","gene_name":"solute carrier family 7 member 14 [Source:HGNC Symbol;Acc:HGNC:29326]","synonyms":"PPP1R142,KIAA1613","biotype":"protein_coding","ncbi_id":"57709","summary":"This gene is predicted to encode a glycosylated, cationic amino acid transporter protein with 14 transmembrane domains. This gene is primarily expressed in skin fibroblasts, neural tissue, and primary endothelial cells and its protein is predicted to mediate lysosomal uptake of cationic amino acids. Mutations in this gene are associated with autosomal recessive retinitis pigmentosa. In mice, this gene is expressed in the photoreceptor layer of the retina where its expression increases over the course of retinal development and persists in the mature retina. [provided by RefSeq, Apr 2014]","start":170459584,"end":170586074,"strand":-1,"description":"solute carrier family 7 member 14 [Source:HGNC Symbol;Acc:HGNC:29326]"}, {"versioned_ensembl_gene_id":"ENSG00000185955.4","gene_symbol":"C7orf61","gene_name":"chromosome 7 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:22135]","synonyms":"IMAGE:4839025","biotype":"protein_coding","ncbi_id":"402573","summary":null,"start":100456615,"end":100464271,"strand":-1,"description":"chromosome 7 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:22135]"}, {"versioned_ensembl_gene_id":"ENSG00000229911.2","gene_symbol":"AL139148.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118712999,"end":118713678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013297.10","gene_symbol":"CLDN11","gene_name":"claudin 11 [Source:HGNC Symbol;Acc:HGNC:8514]","synonyms":"OTM,OSP","biotype":"protein_coding","ncbi_id":"5010","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]","start":170418865,"end":170860380,"strand":1,"description":"claudin 11 [Source:HGNC Symbol;Acc:HGNC:8514]"}, {"versioned_ensembl_gene_id":"ENSG00000261317.1","gene_symbol":"AC092143.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89969791,"end":89972544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174807.3","gene_symbol":"CD248","gene_name":"CD248 molecule [Source:HGNC Symbol;Acc:HGNC:18219]","synonyms":"TEM1,CD164L1","biotype":"protein_coding","ncbi_id":"57124","summary":null,"start":66314487,"end":66317044,"strand":-1,"description":"CD248 molecule [Source:HGNC Symbol;Acc:HGNC:18219]"}, {"versioned_ensembl_gene_id":"ENSG00000103023.11","gene_symbol":"PRSS54","gene_name":"protease, serine 54 [Source:HGNC Symbol;Acc:HGNC:26336]","synonyms":"KLKBL4,FLJ25339,CT67","biotype":"protein_coding","ncbi_id":"221191","summary":"This gene encodes a putative serine-type endopeptidase containing the peptidase S1 domain. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":58279997,"end":58295047,"strand":-1,"description":"protease, serine 54 [Source:HGNC Symbol;Acc:HGNC:26336]"}, {"versioned_ensembl_gene_id":"ENSG00000274525.1","gene_symbol":"AC008443.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":181291673,"end":181295572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273837.1","gene_symbol":"AC018755.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51639478,"end":51639931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133985.2","gene_symbol":"TTC9","gene_name":"tetratricopeptide repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20267]","synonyms":"TTC9A,KIAA0227","biotype":"protein_coding","ncbi_id":"23508","summary":"This gene encodes a protein that contains three tetratricopeptide repeats. The gene has been shown to be hormonally regulated in breast cancer cells and may play a role in cancer cell invasion and metastasis. [provided by RefSeq, Mar 2009]","start":70641787,"end":70675360,"strand":1,"description":"tetratricopeptide repeat domain 9 [Source:HGNC Symbol;Acc:HGNC:20267]"}, {"versioned_ensembl_gene_id":"ENSG00000198812.4","gene_symbol":"LRRC10","gene_name":"leucine rich repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:20264]","synonyms":"LRRC10A,HRLRRP","biotype":"protein_coding","ncbi_id":"376132","summary":null,"start":69608564,"end":69611162,"strand":-1,"description":"leucine rich repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:20264]"}, {"versioned_ensembl_gene_id":"ENSG00000275181.2","gene_symbol":"GPR20","gene_name":"G protein-coupled receptor 20 [Source:HGNC Symbol;Acc:HGNC:4475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2843","summary":null,"start":141356500,"end":141367267,"strand":-1,"description":"G protein-coupled receptor 20 [Source:HGNC Symbol;Acc:HGNC:4475]"}, {"versioned_ensembl_gene_id":"ENSG00000176124.11","gene_symbol":"DLEU1","gene_name":"deleted in lymphocytic leukemia 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13747]","synonyms":"XTP6,NCRNA00021,LINC00021,LEU1,DLB1,BCMS1,BCMS","biotype":"processed_transcript","ncbi_id":"10301","summary":null,"start":50082171,"end":50723236,"strand":1,"description":"deleted in lymphocytic leukemia 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13747]"}, {"versioned_ensembl_gene_id":"ENSG00000271386.1","gene_symbol":"SRGNP1","gene_name":"serglycin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480246","summary":null,"start":78285838,"end":78286288,"strand":1,"description":"serglycin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49107]"}, {"versioned_ensembl_gene_id":"ENSG00000138696.10","gene_symbol":"BMPR1B","gene_name":"bone morphogenetic protein receptor type 1B [Source:HGNC Symbol;Acc:HGNC:1077]","synonyms":"CDw293,ALK6","biotype":"protein_coding","ncbi_id":"658","summary":"This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":94757968,"end":95158448,"strand":1,"description":"bone morphogenetic protein receptor type 1B [Source:HGNC Symbol;Acc:HGNC:1077]"}, {"versioned_ensembl_gene_id":"ENSG00000180479.13","gene_symbol":"ZNF571","gene_name":"zinc finger protein 571 [Source:HGNC Symbol;Acc:HGNC:25000]","synonyms":"HSPC059","biotype":"protein_coding","ncbi_id":"51276","summary":null,"start":37554782,"end":37594790,"strand":-1,"description":"zinc finger protein 571 [Source:HGNC Symbol;Acc:HGNC:25000]"}, {"versioned_ensembl_gene_id":"ENSG00000253103.1","gene_symbol":"LINC01609","gene_name":"long intergenic non-protein coding RNA 1609 [Source:HGNC Symbol;Acc:HGNC:51663]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927487","summary":null,"start":111098961,"end":111236203,"strand":-1,"description":"long intergenic non-protein coding RNA 1609 [Source:HGNC Symbol;Acc:HGNC:51663]"}, {"versioned_ensembl_gene_id":"ENSG00000198471.1","gene_symbol":"RTP2","gene_name":"receptor transporter protein 2 [Source:HGNC Symbol;Acc:HGNC:32486]","synonyms":"MGC78665,Z3CXXC2","biotype":"protein_coding","ncbi_id":"344892","summary":null,"start":187698259,"end":187702557,"strand":-1,"description":"receptor transporter protein 2 [Source:HGNC Symbol;Acc:HGNC:32486]"}, {"versioned_ensembl_gene_id":"ENSG00000279484.1","gene_symbol":"KLHL30-AS1","gene_name":"KLHL30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31018]","synonyms":"C2orf19","biotype":"TEC","ncbi_id":"394261","summary":null,"start":238152889,"end":238155994,"strand":-1,"description":"KLHL30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31018]"}, {"versioned_ensembl_gene_id":"ENSG00000227069.1","gene_symbol":"CNN2P2","gene_name":"calponin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39527]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642888","summary":null,"start":40346144,"end":40347052,"strand":-1,"description":"calponin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39527]"}, {"versioned_ensembl_gene_id":"ENSG00000242512.8","gene_symbol":"LINC01206","gene_name":"long intergenic non-protein coding RNA 1206 [Source:HGNC Symbol;Acc:HGNC:49637]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996490","summary":null,"start":181952343,"end":182010678,"strand":1,"description":"long intergenic non-protein coding RNA 1206 [Source:HGNC Symbol;Acc:HGNC:49637]"}, {"versioned_ensembl_gene_id":"ENSG00000213465.7","gene_symbol":"ARL2","gene_name":"ADP ribosylation factor like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:693]","synonyms":"ARFL2","biotype":"protein_coding","ncbi_id":"402","summary":"This gene encodes a small GTP-binding protein of the RAS superfamily which functions as an ADP-ribosylation factor (ARF). The encoded protein is one of a functionally distinct group of ARF-like genes. [provided by RefSeq, Jul 2008]","start":65014113,"end":65022184,"strand":1,"description":"ADP ribosylation factor like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:693]"}, {"versioned_ensembl_gene_id":"ENSG00000270775.1","gene_symbol":"AP000436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65025390,"end":65026515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214216.10","gene_symbol":"IQCJ","gene_name":"IQ motif containing J [Source:HGNC Symbol;Acc:HGNC:32406]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654502","summary":null,"start":158962928,"end":159266307,"strand":1,"description":"IQ motif containing J [Source:HGNC Symbol;Acc:HGNC:32406]"}, {"versioned_ensembl_gene_id":"ENSG00000237979.1","gene_symbol":"AC007389.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65500993,"end":65502138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271072.1","gene_symbol":"PHBP20","gene_name":"prohibitin pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130579","summary":null,"start":72450657,"end":72451474,"strand":1,"description":"prohibitin pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51553]"}, {"versioned_ensembl_gene_id":"ENSG00000227902.2","gene_symbol":"AC062032.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146879909,"end":146898218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229593.1","gene_symbol":"SUCLA2P3","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38103]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421648","summary":null,"start":25079901,"end":25081689,"strand":-1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38103]"}, {"versioned_ensembl_gene_id":"ENSG00000277509.1","gene_symbol":"AC099669.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44528955,"end":44529391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203814.6","gene_symbol":"HIST2H2BF","gene_name":"histone cluster 2 H2B family member f [Source:HGNC Symbol;Acc:HGNC:24700]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440689","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-dependent histone that is a member of the histone H2B family and is found in a histone cluster on chromosome 1. [provided by RefSeq, Aug 2015]","start":149782689,"end":149812373,"strand":-1,"description":"histone cluster 2 H2B family member f [Source:HGNC Symbol;Acc:HGNC:24700]"}, {"versioned_ensembl_gene_id":"ENSG00000226500.2","gene_symbol":"AC243772.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149754301,"end":149754710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244540.2","gene_symbol":"AC087884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51106817,"end":51107144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162063.12","gene_symbol":"CCNF","gene_name":"cyclin F [Source:HGNC Symbol;Acc:HGNC:1591]","synonyms":"FBXO1,FBX1","biotype":"protein_coding","ncbi_id":"899","summary":"This gene encodes a member of the cyclin family. Cyclins are important regulators of cell cycle transitions through their ability to bind and activate cyclin-dependent protein kinases. This member also belongs to the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it was one of the first proteins in which the F-box motif was identified. [provided by RefSeq, Jul 2008]","start":2429394,"end":2458854,"strand":1,"description":"cyclin F [Source:HGNC Symbol;Acc:HGNC:1591]"}, {"versioned_ensembl_gene_id":"ENSG00000110719.9","gene_symbol":"TCIRG1","gene_name":"T-cell immune regulator 1, ATPase H+ transporting V0 subunit a3 [Source:HGNC Symbol;Acc:HGNC:11647]","synonyms":"OC116,OC-116,ATP6V0A3,ATP6N1C,Atp6i,a3,TIRC7","biotype":"protein_coding","ncbi_id":"10312","summary":"This gene encodes a subunit of a large protein complex known as a vacuolar H+-ATPase (V-ATPase). The protein complex acts as a pump to move protons across the membrane. This movement of protons helps regulate the pH of cells and their surrounding environment. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor-mediated endocytosis. V-ATPase is comprised of a cytosolic V1 domain and a transmembrane V0 domain. Alternative splicing results in multiple transcript variants. Mutations in this gene are associated with infantile malignant osteopetrosis. [provided by RefSeq, May 2017]","start":68039016,"end":68050895,"strand":1,"description":"T-cell immune regulator 1, ATPase H+ transporting V0 subunit a3 [Source:HGNC Symbol;Acc:HGNC:11647]"}, {"versioned_ensembl_gene_id":"ENSG00000256029.5","gene_symbol":"AL590560.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":159857900,"end":159873053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250640.2","gene_symbol":"AC090835.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14987671,"end":14988694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255043.1","gene_symbol":"NAV2-AS5","gene_name":"NAV2 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:40740]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874012","summary":null,"start":19502672,"end":19507229,"strand":-1,"description":"NAV2 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:40740]"}, {"versioned_ensembl_gene_id":"ENSG00000230416.3","gene_symbol":"OR5M4P","gene_name":"olfactory receptor family 5 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14808]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79518","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56448668,"end":56449592,"strand":1,"description":"olfactory receptor family 5 subfamily M member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14808]"}, {"versioned_ensembl_gene_id":"ENSG00000279961.2","gene_symbol":"OR5R1","gene_name":"olfactory receptor family 5 subfamily R member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14841]","synonyms":"OR5R1P","biotype":"polymorphic_pseudogene","ncbi_id":"219479","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":56417258,"end":56418232,"strand":-1,"description":"olfactory receptor family 5 subfamily R member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14841]"}, {"versioned_ensembl_gene_id":"ENSG00000229889.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29474955,"end":29476001,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000272987.1","gene_symbol":"AP002512.3","gene_name":null,"synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":null,"summary":null,"start":56412696,"end":56413680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154611.14","gene_symbol":"PSMA8","gene_name":"proteasome subunit alpha 8 [Source:HGNC Symbol;Acc:HGNC:22985]","synonyms":"PSMA7L,MGC26605","biotype":"protein_coding","ncbi_id":"143471","summary":null,"start":26133852,"end":26193355,"strand":1,"description":"proteasome subunit alpha 8 [Source:HGNC Symbol;Acc:HGNC:22985]"}, {"versioned_ensembl_gene_id":"ENSG00000273018.5","gene_symbol":"AC107983.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18511221,"end":18551705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279462.1","gene_symbol":"AC093028.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125300936,"end":125301917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158186.12","gene_symbol":"MRAS","gene_name":"muscle RAS oncogene homolog [Source:HGNC Symbol;Acc:HGNC:7227]","synonyms":"RRAS3,R-RAS3,M-RAs","biotype":"protein_coding","ncbi_id":"22808","summary":"This gene encodes a member of the Ras family of small GTPases. These membrane-associated proteins function as signal transducers in multiple processes including cell growth and differentiation, and dysregulation of Ras signaling has been associated with many types of cancer. The encoded protein may play a role in the tumor necrosis factor-alpha and MAP kinase signaling pathways. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":138347648,"end":138405534,"strand":1,"description":"muscle RAS oncogene homolog [Source:HGNC Symbol;Acc:HGNC:7227]"}, {"versioned_ensembl_gene_id":"ENSG00000065154.11","gene_symbol":"OAT","gene_name":"ornithine aminotransferase [Source:HGNC Symbol;Acc:HGNC:8091]","synonyms":"HOGA","biotype":"protein_coding","ncbi_id":"4942","summary":"This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome. [provided by RefSeq, Jan 2010]","start":124397303,"end":124418976,"strand":-1,"description":"ornithine aminotransferase [Source:HGNC Symbol;Acc:HGNC:8091]"}, {"versioned_ensembl_gene_id":"ENSG00000241318.3","gene_symbol":"WDR82P2","gene_name":"WD repeat domain 82 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33513]","synonyms":"WDR82C","biotype":"processed_pseudogene","ncbi_id":"441891","summary":null,"start":91534666,"end":91535593,"strand":-1,"description":"WD repeat domain 82 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33513]"}, {"versioned_ensembl_gene_id":"ENSG00000227599.1","gene_symbol":"AL031676.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42968743,"end":42971492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144063.3","gene_symbol":"MALL","gene_name":"mal, T-cell differentiation protein like [Source:HGNC Symbol;Acc:HGNC:6818]","synonyms":"BENE","biotype":"protein_coding","ncbi_id":"7851","summary":"This gene encodes an element of the machinery for raft-mediated trafficking in endothelial cells. The encoded protein, a member of the MAL proteolipid family, predominantly localizes in glycolipid- and cholesterol-enriched membrane (GEM) rafts. It interacts with caveolin-1. [provided by RefSeq, Jul 2008]","start":110083870,"end":110116566,"strand":-1,"description":"mal, T-cell differentiation protein like [Source:HGNC Symbol;Acc:HGNC:6818]"}, {"versioned_ensembl_gene_id":"ENSG00000269050.1","gene_symbol":"AC011455.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38870159,"end":38873763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255133.1","gene_symbol":"AC113192.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33814877,"end":33822095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229730.2","gene_symbol":"AC013268.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110012265,"end":110012601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112739.16","gene_symbol":"PRPF4B","gene_name":"pre-mRNA processing factor 4B [Source:HGNC Symbol;Acc:HGNC:17346]","synonyms":"KIAA0536,Prp4,PR4H","biotype":"protein_coding","ncbi_id":"8899","summary":"Pre-mRNA splicing occurs in two sequential transesterification steps, and the protein encoded by this gene is thought to be involved in pre-mRNA splicing and in signal transduction. This protein belongs to a kinase family that includes serine/arginine-rich protein-specific kinases and cyclin-dependent kinases (CDKs). This protein is regarded as a CDK-like kinase (Clk) with homology to mitogen-activated protein kinases (MAPKs). [provided by RefSeq, Jul 2008]","start":4021267,"end":4064983,"strand":1,"description":"pre-mRNA processing factor 4B [Source:HGNC Symbol;Acc:HGNC:17346]"}, {"versioned_ensembl_gene_id":"ENSG00000181693.8","gene_symbol":"OR8H1","gene_name":"olfactory receptor family 8 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14824]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219469","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56288462,"end":56292254,"strand":-1,"description":"olfactory receptor family 8 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14824]"}, {"versioned_ensembl_gene_id":"ENSG00000113448.18","gene_symbol":"PDE4D","gene_name":"phosphodiesterase 4D [Source:HGNC Symbol;Acc:HGNC:8783]","synonyms":"DPDE3","biotype":"protein_coding","ncbi_id":"5144","summary":"This gene encodes one of four mammalian counterparts to the fruit fly 'dunce' gene. The encoded protein has 3',5'-cyclic-AMP phosphodiesterase activity and degrades cAMP, which acts as a signal transduction molecule in multiple cell types. This gene uses different promoters to generate multiple alternatively spliced transcript variants that encode functional proteins.[provided by RefSeq, Sep 2009]","start":58969038,"end":60522120,"strand":-1,"description":"phosphodiesterase 4D [Source:HGNC Symbol;Acc:HGNC:8783]"}, {"versioned_ensembl_gene_id":"ENSG00000258915.1","gene_symbol":"BHLHB9P1","gene_name":"basic helix-loop-helix family member b9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100431177","summary":null,"start":80981988,"end":80983638,"strand":1,"description":"basic helix-loop-helix family member b9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51373]"}, {"versioned_ensembl_gene_id":"ENSG00000174957.1","gene_symbol":"OR5J2","gene_name":"olfactory receptor family 5 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:19612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282775","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56176618,"end":56177556,"strand":1,"description":"olfactory receptor family 5 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:19612]"}, {"versioned_ensembl_gene_id":"ENSG00000238074.5","gene_symbol":"TSPY9P","gene_name":"testis specific protein, Y-linked 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:37472]","synonyms":"TSPY9","biotype":"unprocessed_pseudogene","ncbi_id":"728132","summary":null,"start":9487313,"end":9489893,"strand":1,"description":"testis specific protein, Y-linked 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:37472]"}, {"versioned_ensembl_gene_id":"ENSG00000269951.1","gene_symbol":"AC090181.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":77067654,"end":77068325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232781.1","gene_symbol":"BX927167.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026645,"end":29027572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204482.10","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31586124,"end":31588909,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000252364.1","gene_symbol":"RNA5SP360","gene_name":"RNA, 5S ribosomal pseudogene 360 [Source:HGNC Symbol;Acc:HGNC:43260]","synonyms":"RN5S360","biotype":"rRNA","ncbi_id":"100873619","summary":null,"start":41658676,"end":41658793,"strand":1,"description":"RNA, 5S ribosomal pseudogene 360 [Source:HGNC Symbol;Acc:HGNC:43260]"}, {"versioned_ensembl_gene_id":"ENSG00000265460.6","gene_symbol":"AC015910.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":39238466,"end":39250818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000051108.14","gene_symbol":"HERPUD1","gene_name":"homocysteine inducible ER protein with ubiquitin like domain 1 [Source:HGNC Symbol;Acc:HGNC:13744]","synonyms":"SUP,Mif1,KIAA0025,HERP","biotype":"protein_coding","ncbi_id":"9709","summary":"The accumulation of unfolded proteins in the endoplasmic reticulum (ER) triggers the ER stress response. This response includes the inhibition of translation to prevent further accumulation of unfolded proteins, the increased expression of proteins involved in polypeptide folding, known as the unfolded protein response (UPR), and the destruction of misfolded proteins by the ER-associated protein degradation (ERAD) system. This gene may play a role in both UPR and ERAD. Its expression is induced by UPR and it has an ER stress response element in its promoter region while the encoded protein has an N-terminal ubiquitin-like domain which may interact with the ERAD system. This protein has been shown to interact with presenilin proteins and to increase the level of amyloid-beta protein following its overexpression. Alternative splicing of this gene produces multiple transcript variants encoding different isoforms. The full-length nature of all transcript variants has not been determined. [provided by RefSeq, Jan 2013]","start":56932048,"end":56944863,"strand":1,"description":"homocysteine inducible ER protein with ubiquitin like domain 1 [Source:HGNC Symbol;Acc:HGNC:13744]"}, {"versioned_ensembl_gene_id":"ENSG00000223912.1","gene_symbol":"EEF1A1P36","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421820","summary":null,"start":132271982,"end":132273332,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37914]"}, {"versioned_ensembl_gene_id":"ENSG00000232120.1","gene_symbol":"AL357375.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64377795,"end":64412779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225482.1","gene_symbol":"RPS6P14","gene_name":"ribosomal protein S6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36738]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131396","summary":null,"start":48292699,"end":48293417,"strand":1,"description":"ribosomal protein S6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36738]"}, {"versioned_ensembl_gene_id":"ENSG00000283684.1","gene_symbol":"AC013268.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":109937438,"end":109985124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284337.1","gene_symbol":"AC013271.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":109898432,"end":109968557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132703.3","gene_symbol":"APCS","gene_name":"amyloid P component, serum [Source:HGNC Symbol;Acc:HGNC:584]","synonyms":"SAP,PTX2,MGC88159","biotype":"protein_coding","ncbi_id":"325","summary":"The protein encoded by this gene is a glycoprotein, belonging to the pentraxin family of proteins, which has a characteristic pentameric organization. These family members have considerable sequence homology which is thought to be the result of gene duplication. The binding of the encoded protein to proteins in the pathological amyloid cross-beta fold suggests its possible role as a chaperone. This protein is also thought to control the degradation of chromatin. It has been demonstrated that this protein binds to apoptotic cells at an early stage, which raises the possibility that it is involved in dealing with apoptotic cells in vivo. [provided by RefSeq, Sep 2008]","start":159587825,"end":159588865,"strand":1,"description":"amyloid P component, serum [Source:HGNC Symbol;Acc:HGNC:584]"}, {"versioned_ensembl_gene_id":"ENSG00000275445.1","gene_symbol":"AC092119.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22007480,"end":22008062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185716.11","gene_symbol":"C16orf52","gene_name":"chromosome 16 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:27087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730094","summary":null,"start":22007638,"end":22087534,"strand":1,"description":"chromosome 16 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:27087]"}, {"versioned_ensembl_gene_id":"ENSG00000081026.18","gene_symbol":"MAGI3","gene_name":"membrane associated guanylate kinase, WW and PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29647]","synonyms":"MAGI-3","biotype":"protein_coding","ncbi_id":"260425","summary":null,"start":113390749,"end":113685923,"strand":1,"description":"membrane associated guanylate kinase, WW and PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29647]"}, {"versioned_ensembl_gene_id":"ENSG00000182901.16","gene_symbol":"RGS7","gene_name":"regulator of G protein signaling 7 [Source:HGNC Symbol;Acc:HGNC:10003]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6000","summary":null,"start":240775515,"end":241357230,"strand":-1,"description":"regulator of G protein signaling 7 [Source:HGNC Symbol;Acc:HGNC:10003]"}, {"versioned_ensembl_gene_id":"ENSG00000248639.2","gene_symbol":"AC098799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68293127,"end":68294364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261087.1","gene_symbol":"AP003469.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101166805,"end":101169629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160714.9","gene_symbol":"UBE2Q1","gene_name":"ubiquitin conjugating enzyme E2 Q1 [Source:HGNC Symbol;Acc:HGNC:15698]","synonyms":"UBE2Q,PRO3094,NICE-5","biotype":"protein_coding","ncbi_id":"55585","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s), and ubiquitin-protein ligases (E3s). This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein is 98% identical to the mouse counterpart. [provided by RefSeq, Jul 2008]","start":154548577,"end":154559028,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q1 [Source:HGNC Symbol;Acc:HGNC:15698]"}, {"versioned_ensembl_gene_id":"ENSG00000229780.1","gene_symbol":"UBE2Q1-AS1","gene_name":"UBE2Q1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40722]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874097","summary":null,"start":154553609,"end":154555017,"strand":1,"description":"UBE2Q1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40722]"}, {"versioned_ensembl_gene_id":"ENSG00000238037.1","gene_symbol":"OOSP1P1","gene_name":"oocyte secreted protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49240]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480251","summary":null,"start":44155028,"end":44155301,"strand":-1,"description":"oocyte secreted protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49240]"}, {"versioned_ensembl_gene_id":"ENSG00000170835.14","gene_symbol":"CEL","gene_name":"carboxyl ester lipase [Source:HGNC Symbol;Acc:HGNC:1848]","synonyms":"MODY8,BSSL","biotype":"protein_coding","ncbi_id":"1056","summary":"The protein encoded by this gene is a glycoprotein secreted from the pancreas into the digestive tract and from the lactating mammary gland into human milk. The physiological role of this protein is in cholesterol and lipid-soluble vitamin ester hydrolysis and absorption. This encoded protein promotes large chylomicron production in the intestine. Also its presence in plasma suggests its interactions with cholesterol and oxidized lipoproteins to modulate the progression of atherosclerosis. In pancreatic tumoral cells, this encoded protein is thought to be sequestrated within the Golgi compartment and is probably not secreted. This gene contains a variable number of tandem repeat (VNTR) polymorphism in the coding region that may influence the function of the encoded protein. [provided by RefSeq, Jul 2008]","start":133061978,"end":133071861,"strand":1,"description":"carboxyl ester lipase [Source:HGNC Symbol;Acc:HGNC:1848]"}, {"versioned_ensembl_gene_id":"ENSG00000187848.12","gene_symbol":"P2RX2","gene_name":"purinergic receptor P2X 2 [Source:HGNC Symbol;Acc:HGNC:15459]","synonyms":"P2X2,DFNA41","biotype":"protein_coding","ncbi_id":"22953","summary":"The product of this gene belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel. Binding to ATP mediates synaptic transmission between neurons and from neurons to smooth muscle. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Aug 2013]","start":132618780,"end":132622386,"strand":1,"description":"purinergic receptor P2X 2 [Source:HGNC Symbol;Acc:HGNC:15459]"}, {"versioned_ensembl_gene_id":"ENSG00000136877.14","gene_symbol":"FPGS","gene_name":"folylpolyglutamate synthase [Source:HGNC Symbol;Acc:HGNC:3824]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2356","summary":"This gene encodes the folylpolyglutamate synthetase enzyme. This enzyme has a central role in establishing and maintaining both cytosolic and mitochondrial folylpolyglutamate concentrations and, therefore, is essential for folate homeostasis and the survival of proliferating cells. This enzyme catalyzes the ATP-dependent addition of glutamate moieties to folate and folate derivatives. Alternative splicing results in transcript variants encoding different isoforms. [provided by RefSeq, Jan 2014]","start":127794597,"end":127814327,"strand":1,"description":"folylpolyglutamate synthase [Source:HGNC Symbol;Acc:HGNC:3824]"}, {"versioned_ensembl_gene_id":"ENSG00000244380.1","gene_symbol":"AC134772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48440352,"end":48446656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130956.13","gene_symbol":"HABP4","gene_name":"hyaluronan binding protein 4 [Source:HGNC Symbol;Acc:HGNC:17062]","synonyms":"SERBP1L,IHABP4","biotype":"protein_coding","ncbi_id":"22927","summary":null,"start":96450201,"end":96491336,"strand":1,"description":"hyaluronan binding protein 4 [Source:HGNC Symbol;Acc:HGNC:17062]"}, {"versioned_ensembl_gene_id":"ENSG00000116251.9","gene_symbol":"RPL22","gene_name":"ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:10315]","synonyms":"EAP,L22","biotype":"protein_coding","ncbi_id":"6146","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a cytoplasmic ribosomal protein that is a component of the 60S subunit. The protein belongs to the L22E family of ribosomal proteins. Its initiating methionine residue is post-translationally removed. The protein can bind specifically to Epstein-Barr virus-encoded RNAs (EBERs) 1 and 2. The mouse protein has been shown to be capable of binding to heparin. Transcript variants utilizing alternative polyA signals exist. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. It was previously thought that this gene mapped to 3q26 and that it was fused to the acute myeloid leukemia 1 (AML1) gene located at 21q22 in some therapy-related myelodysplastic syndrome patients with 3;21 translocations; however, these fusions actually involve a ribosomal protein L22 pseudogene located at 3q26, and this gene actually maps to 1p36.3-p36.2. [provided by RefSeq, Jul 2008]","start":6181269,"end":6209389,"strand":-1,"description":"ribosomal protein L22 [Source:HGNC Symbol;Acc:HGNC:10315]"}, {"versioned_ensembl_gene_id":"ENSG00000271890.1","gene_symbol":"OR10AE1P","gene_name":"olfactory receptor family 10 subfamily AE member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14990]","synonyms":"OR10AE2P","biotype":"unprocessed_pseudogene","ncbi_id":"81486","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159581620,"end":159582648,"strand":-1,"description":"olfactory receptor family 10 subfamily AE member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14990]"}, {"versioned_ensembl_gene_id":"ENSG00000271486.1","gene_symbol":"AP000403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19620695,"end":19621545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277597.1","gene_symbol":"AC130343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1684726,"end":1685151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271136.1","gene_symbol":"AL592504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34516920,"end":34517358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234681.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29821066,"end":29822046,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000231100.1","gene_symbol":"AL606752.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":159557368,"end":159558200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227704.1","gene_symbol":"AL354892.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169725504,"end":169738992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149735.6","gene_symbol":"GPHA2","gene_name":"glycoprotein hormone alpha 2 [Source:HGNC Symbol;Acc:HGNC:18054]","synonyms":"ZSIG51,MGC126572,GPA2,A2","biotype":"protein_coding","ncbi_id":"170589","summary":"GPHA2 is a cystine knot-forming polypeptide and a subunit of the dimeric glycoprotein hormone family (Hsu et al., 2002 [PubMed 12089349]).[supplied by OMIM, Mar 2008]","start":64934471,"end":64935888,"strand":-1,"description":"glycoprotein hormone alpha 2 [Source:HGNC Symbol;Acc:HGNC:18054]"}, {"versioned_ensembl_gene_id":"ENSG00000171872.4","gene_symbol":"KLF17","gene_name":"Kruppel like factor 17 [Source:HGNC Symbol;Acc:HGNC:18830]","synonyms":"FLJ40160,ZNF393,Zfp393","biotype":"protein_coding","ncbi_id":"128209","summary":null,"start":44118850,"end":44135140,"strand":1,"description":"Kruppel like factor 17 [Source:HGNC Symbol;Acc:HGNC:18830]"}, {"versioned_ensembl_gene_id":"ENSG00000007541.16","gene_symbol":"PIGQ","gene_name":"phosphatidylinositol glycan anchor biosynthesis class Q [Source:HGNC Symbol;Acc:HGNC:14135]","synonyms":"hGPI1,GPI1","biotype":"protein_coding","ncbi_id":"9091","summary":"This gene is involved in the first step in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This gene encodes a N-acetylglucosaminyl transferase component that is part of the complex that catalyzes transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":566995,"end":584136,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class Q [Source:HGNC Symbol;Acc:HGNC:14135]"}, {"versioned_ensembl_gene_id":"ENSG00000234819.1","gene_symbol":"AL353705.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78219120,"end":78219357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231922.1","gene_symbol":"AL138479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53917270,"end":53917753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258992.6","gene_symbol":"TSPY1","gene_name":"testis specific protein, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:12381]","synonyms":"TSPY,CT78","biotype":"protein_coding","ncbi_id":"7258","summary":"The protein encoded by this gene is found only in testicular tissue and may be involved in spermatogenesis. Many functional paralogs and pseudogenes of this gene are present in a cluster in humans, but only a single, nonfunctional orthologous gene is found in mouse. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":9466955,"end":9469748,"strand":1,"description":"testis specific protein, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:12381]"}, {"versioned_ensembl_gene_id":"ENSG00000236866.5","gene_symbol":"AL157902.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117596832,"end":117605770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272248.1","gene_symbol":"AL138831.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4018713,"end":4019202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205236.6","gene_symbol":"AC105052.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":102582523,"end":102642869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257511.1","gene_symbol":"AC084824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32726383,"end":32727387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254794.1","gene_symbol":"AP000676.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87917948,"end":87917999,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284620.1","gene_symbol":"AF228730.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7092102,"end":7187299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273536.1","gene_symbol":"AC121758.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56840973,"end":56841273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235113.1","gene_symbol":"AL161932.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32109861,"end":32111666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234335.1","gene_symbol":"RPS4XP11","gene_name":"ribosomal protein S4X pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37013]","synonyms":"RPS4P11","biotype":"processed_pseudogene","ncbi_id":"441550","summary":null,"start":32102522,"end":32103293,"strand":-1,"description":"ribosomal protein S4X pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37013]"}, {"versioned_ensembl_gene_id":"ENSG00000260604.2","gene_symbol":"AL590004.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3904920,"end":3911979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248257.7","gene_symbol":"PSG10P","gene_name":"pregnancy specific beta-1-glycoprotein 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:9515]","synonyms":"PSG12,PSG10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653492","summary":"The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":42839368,"end":42855718,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:9515]"}, {"versioned_ensembl_gene_id":"ENSG00000247950.6","gene_symbol":"SEC24B-AS1","gene_name":"SEC24B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44003]","synonyms":"1/2-SBSRNA4","biotype":"antisense_RNA","ncbi_id":"100533182","summary":"This lncRNA contains a single Alu element which, along with 1/2-sbsRNA3, appears to target the 3' UTR Alu element in MTAP. Downregulation of the RNA appears to up-regulate the target. [provided by RefSeq, Feb 2011]","start":109347475,"end":109433817,"strand":-1,"description":"SEC24B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44003]"}, {"versioned_ensembl_gene_id":"ENSG00000272755.1","gene_symbol":"AC245297.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149264252,"end":149264816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235710.4","gene_symbol":"AL109810.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":231184098,"end":231187627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231625.4","gene_symbol":"AC115989.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19615789,"end":19633825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186474.15","gene_symbol":"KLK12","gene_name":"kallikrein related peptidase 12 [Source:HGNC Symbol;Acc:HGNC:6360]","synonyms":"KLK-L5","biotype":"protein_coding","ncbi_id":"43849","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Alternate splicing of this gene results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":51029092,"end":51035230,"strand":-1,"description":"kallikrein related peptidase 12 [Source:HGNC Symbol;Acc:HGNC:6360]"}, {"versioned_ensembl_gene_id":"ENSG00000232622.1","gene_symbol":"AC114482.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84636158,"end":84637106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250820.1","gene_symbol":"AC138965.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":175906939,"end":175958538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196550.10","gene_symbol":"FAM72A","gene_name":"family with sequence similarity 72 member A [Source:HGNC Symbol;Acc:HGNC:24044]","synonyms":"UGENE,RP11-312O7.1,MGC57827,LMPIP","biotype":"protein_coding","ncbi_id":"729533","summary":null,"start":206186179,"end":206204414,"strand":-1,"description":"family with sequence similarity 72 member A [Source:HGNC Symbol;Acc:HGNC:24044]"}, {"versioned_ensembl_gene_id":"ENSG00000276523.1","gene_symbol":"AC025287.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75572185,"end":75572685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135702.14","gene_symbol":"CHST5","gene_name":"carbohydrate sulfotransferase 5 [Source:HGNC Symbol;Acc:HGNC:1973]","synonyms":"I-GLCNAC-6-ST,FLJ22167","biotype":"protein_coding","ncbi_id":"23563","summary":"The protein encoded by this gene belongs to the Gal/GalNAc/GlcNAc 6-O-sulfotransferase (GST) family, members of which catalyze the transfer of sulfate to position 6 of galactose (Gal), N-acetylgalactosamine (GalNAc), or N-acetylglucosamine (GlcNAc) residues within proteoglycans, and sulfation of O-linked sugars of mucin-type acceptors. Carbohydrate sulfation plays a critical role in many biologic processes. This gene is predominantly expressed in colon and small intestine. [provided by RefSeq, Aug 2011]","start":75528535,"end":75535247,"strand":-1,"description":"carbohydrate sulfotransferase 5 [Source:HGNC Symbol;Acc:HGNC:1973]"}, {"versioned_ensembl_gene_id":"ENSG00000250039.3","gene_symbol":"AC096719.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21949015,"end":22330330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259992.1","gene_symbol":"AC025287.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75541399,"end":75608445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264187.1","gene_symbol":"AC055811.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17202649,"end":17237185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204070.9","gene_symbol":"SYS1","gene_name":"SYS1, golgi trafficking protein [Source:HGNC Symbol;Acc:HGNC:16162]","synonyms":"dJ453C12.4,C20orf169","biotype":"protein_coding","ncbi_id":"90196","summary":"SYS1 forms a complex with ADP-ribosylation factor-related protein ARFRP1 (MIM 604699) and targets ARFRP1 to the Golgi apparatus (Behnia et al., 2004 [PubMed 15077113]).[supplied by OMIM, Aug 2009]","start":45361937,"end":45376798,"strand":1,"description":"SYS1, golgi trafficking protein [Source:HGNC Symbol;Acc:HGNC:16162]"}, {"versioned_ensembl_gene_id":"ENSG00000262583.1","gene_symbol":"AC009163.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75499788,"end":75516280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237610.1","gene_symbol":"OR4C50P","gene_name":"olfactory receptor family 4 subfamily C member 50 pseudogene [Source:HGNC Symbol;Acc:HGNC:31274]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"256190","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54591480,"end":54592409,"strand":1,"description":"olfactory receptor family 4 subfamily C member 50 pseudogene [Source:HGNC Symbol;Acc:HGNC:31274]"}, {"versioned_ensembl_gene_id":"ENSG00000234026.1","gene_symbol":"AL157834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95228243,"end":95231144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214883.4","gene_symbol":"AC024405.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50409042,"end":50422316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250949.1","gene_symbol":"AC093534.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117031200,"end":117038569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108510.9","gene_symbol":"MED13","gene_name":"mediator complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:22474]","synonyms":"TRAP240,THRAP1,KIAA0593","biotype":"protein_coding","ncbi_id":"9969","summary":"This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, possibly by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. The product of this gene is proposed to form a sub-complex with MED12, cyclin C, and CDK8 that can negatively regulate transactivation by mediator. [provided by RefSeq, Jul 2008]","start":61942605,"end":62065282,"strand":-1,"description":"mediator complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:22474]"}, {"versioned_ensembl_gene_id":"ENSG00000214856.11","gene_symbol":"KRT16P1","gene_name":"keratin 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6420]","synonyms":"KRT14P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729252","summary":null,"start":18432051,"end":18442895,"strand":1,"description":"keratin 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6420]"}, {"versioned_ensembl_gene_id":"ENSG00000206245.11","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32332098,"end":32411315,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000074966.10","gene_symbol":"TXK","gene_name":"TXK tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12434]","synonyms":"TKL,RLK,PTK4,PSCTK5,BTKL","biotype":"protein_coding","ncbi_id":"7294","summary":null,"start":48066393,"end":48134256,"strand":-1,"description":"TXK tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12434]"}, {"versioned_ensembl_gene_id":"ENSG00000227163.2","gene_symbol":"AL139220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44087958,"end":44088477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255442.1","gene_symbol":"AC109635.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50170156,"end":50190441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248287.1","gene_symbol":"SCGB1D5P","gene_name":"secretoglobin family 1D member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42735]","synonyms":"SCGB1D1P1","biotype":"processed_pseudogene","ncbi_id":"100874258","summary":null,"start":165517255,"end":165517501,"strand":-1,"description":"secretoglobin family 1D member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42735]"}, {"versioned_ensembl_gene_id":"ENSG00000248489.1","gene_symbol":"LINC02062","gene_name":"long intergenic non-protein coding RNA 2062 [Source:HGNC Symbol;Acc:HGNC:52907]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724810","summary":null,"start":98929171,"end":98995013,"strand":1,"description":"long intergenic non-protein coding RNA 2062 [Source:HGNC Symbol;Acc:HGNC:52907]"}, {"versioned_ensembl_gene_id":"ENSG00000233823.1","gene_symbol":"AL356311.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151813276,"end":151814179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260595.1","gene_symbol":"OR4C49P","gene_name":"olfactory receptor family 4 subfamily C member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31273]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403260","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":50053410,"end":50054309,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31273]"}, {"versioned_ensembl_gene_id":"ENSG00000116212.14","gene_symbol":"LRRC42","gene_name":"leucine rich repeat containing 42 [Source:HGNC Symbol;Acc:HGNC:28792]","synonyms":"MGC8974","biotype":"protein_coding","ncbi_id":"115353","summary":null,"start":53946077,"end":53968168,"strand":1,"description":"leucine rich repeat containing 42 [Source:HGNC Symbol;Acc:HGNC:28792]"}, {"versioned_ensembl_gene_id":"ENSG00000242165.3","gene_symbol":"RN7SL222P","gene_name":"RNA, 7SL, cytoplasmic 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:46238]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481831","summary":null,"start":100641975,"end":100642273,"strand":-1,"description":"RNA, 7SL, cytoplasmic 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:46238]"}, {"versioned_ensembl_gene_id":"ENSG00000258817.1","gene_symbol":"OR4C13","gene_name":"olfactory receptor family 4 subfamily C member 13 [Source:HGNC Symbol;Acc:HGNC:15169]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283092","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49952391,"end":49953419,"strand":1,"description":"olfactory receptor family 4 subfamily C member 13 [Source:HGNC Symbol;Acc:HGNC:15169]"}, {"versioned_ensembl_gene_id":"ENSG00000231715.1","gene_symbol":"COX6CP2","gene_name":"cytochrome c oxidase subunit 6C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16600]","synonyms":"dJ894K16.1","biotype":"processed_pseudogene","ncbi_id":"170504","summary":null,"start":50479767,"end":50479991,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16600]"}, {"versioned_ensembl_gene_id":"ENSG00000116514.16","gene_symbol":"RNF19B","gene_name":"ring finger protein 19B [Source:HGNC Symbol;Acc:HGNC:26886]","synonyms":"IBRDC3,FLJ90005","biotype":"protein_coding","ncbi_id":"127544","summary":"This gene encodes a multi-pass membrane protein containing two RING-type and one IBR-type zinc finger motifs. The encoded protin is an E3 ubiquitin-protein ligase that plays a role in the cytotoxic effects of natural killer (NK) cells. Alternative splicing results in multiple transcript variants. There are pseudogenes for this gene on chromosomes X and Y in a possible pseudoautosomal region. [provided by RefSeq, Jul 2014]","start":32936445,"end":32964685,"strand":-1,"description":"ring finger protein 19B [Source:HGNC Symbol;Acc:HGNC:26886]"}, {"versioned_ensembl_gene_id":"ENSG00000092421.16","gene_symbol":"SEMA6A","gene_name":"semaphorin 6A [Source:HGNC Symbol;Acc:HGNC:10738]","synonyms":"SEMAQ,SEMA6A1,SEMA,KIAA1368,HT018","biotype":"protein_coding","ncbi_id":"57556","summary":"The transmembrane semaphorin SEMA6A is expressed in developing neural tissue and is required for proper development of the thalamocortical projection (Leighton et al., 2001 [PubMed 11242070]).[supplied by OMIM, Feb 2011]","start":116443616,"end":116574934,"strand":-1,"description":"semaphorin 6A [Source:HGNC Symbol;Acc:HGNC:10738]"}, {"versioned_ensembl_gene_id":"ENSG00000273240.1","gene_symbol":"AC013468.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":189763859,"end":189764456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233564.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"CAT56,Em:AB023052.2,Em:AB014077.1","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30635339,"end":30642176,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000204072.3","gene_symbol":"ARMCX7P","gene_name":"armadillo repeat containing, X-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:49917]","synonyms":"GASP10ps,ARMCX6-ps","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653354","summary":null,"start":101597510,"end":101598671,"strand":1,"description":"armadillo repeat containing, X-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:49917]"}, {"versioned_ensembl_gene_id":"ENSG00000100632.10","gene_symbol":"ERH","gene_name":"ERH, mRNA splicing and mitosis factor [Source:HGNC Symbol;Acc:HGNC:3447]","synonyms":"DROER","biotype":"protein_coding","ncbi_id":"2079","summary":null,"start":69380123,"end":69398627,"strand":-1,"description":"ERH, mRNA splicing and mitosis factor [Source:HGNC Symbol;Acc:HGNC:3447]"}, {"versioned_ensembl_gene_id":"ENSG00000254847.1","gene_symbol":"AC009806.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12538083,"end":12540967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237672.1","gene_symbol":"KRR1P1","gene_name":"KRR1, small subunit processome component homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39580]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422486","summary":null,"start":20070250,"end":20072136,"strand":-1,"description":"KRR1, small subunit processome component homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39580]"}, {"versioned_ensembl_gene_id":"ENSG00000278761.1","gene_symbol":"DUX4L11","gene_name":"double homeobox 4 like 11 [Source:HGNC Symbol;Acc:HGNC:38687]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"399839","summary":null,"start":133746641,"end":133747907,"strand":1,"description":"double homeobox 4 like 11 [Source:HGNC Symbol;Acc:HGNC:38687]"}, {"versioned_ensembl_gene_id":"ENSG00000187240.13","gene_symbol":"DYNC2H1","gene_name":"dynein cytoplasmic 2 heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2962]","synonyms":"hdhc11,DYH1B,DNCH2,DHC2,DHC1b","biotype":"protein_coding","ncbi_id":"79659","summary":"This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010]","start":103109431,"end":103479863,"strand":1,"description":"dynein cytoplasmic 2 heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2962]"}, {"versioned_ensembl_gene_id":"ENSG00000196358.10","gene_symbol":"NTNG2","gene_name":"netrin G2 [Source:HGNC Symbol;Acc:HGNC:14288]","synonyms":"NTNG1,Lmnt2,KIAA1857","biotype":"protein_coding","ncbi_id":"84628","summary":null,"start":132161676,"end":132244534,"strand":1,"description":"netrin G2 [Source:HGNC Symbol;Acc:HGNC:14288]"}, {"versioned_ensembl_gene_id":"ENSG00000115602.16","gene_symbol":"IL1RL1","gene_name":"interleukin 1 receptor like 1 [Source:HGNC Symbol;Acc:HGNC:5998]","synonyms":"T1,ST2V,ST2L,ST2,IL33R,FIT-1,DER4","biotype":"protein_coding","ncbi_id":"9173","summary":"The protein encoded by this gene is a member of the interleukin 1 receptor family. Studies of the similar gene in mouse suggested that this receptor can be induced by proinflammatory stimuli, and may be involved in the function of helper T cells. This gene, interleukin 1 receptor, type I (IL1R1), interleukin 1 receptor, type II (IL1R2) and interleukin 1 receptor-like 2 (IL1RL2) form a cytokine receptor gene cluster in a region mapped to chromosome 2q12. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":102311502,"end":102352037,"strand":1,"description":"interleukin 1 receptor like 1 [Source:HGNC Symbol;Acc:HGNC:5998]"}, {"versioned_ensembl_gene_id":"ENSG00000256569.1","gene_symbol":"AC069234.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120721507,"end":120723639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175970.10","gene_symbol":"UNC119B","gene_name":"unc-119 lipid binding chaperone B [Source:HGNC Symbol;Acc:HGNC:16488]","synonyms":"POC7B,MGC5139","biotype":"protein_coding","ncbi_id":"84747","summary":null,"start":120710435,"end":120723640,"strand":1,"description":"unc-119 lipid binding chaperone B [Source:HGNC Symbol;Acc:HGNC:16488]"}, {"versioned_ensembl_gene_id":"ENSG00000173404.4","gene_symbol":"INSM1","gene_name":"INSM transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:6090]","synonyms":"IA1,IA-1","biotype":"protein_coding","ncbi_id":"3642","summary":"Insulinoma-associated 1 (INSM1) gene is intronless and encodes a protein containing both a zinc finger DNA-binding domain and a putative prohormone domain. This gene is a sensitive marker for neuroendocrine differentiation of human lung tumors. [provided by RefSeq, Jul 2008]","start":20368121,"end":20370949,"strand":1,"description":"INSM transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:6090]"}, {"versioned_ensembl_gene_id":"ENSG00000246774.1","gene_symbol":"ZCCHC23","gene_name":"zinc finger CCHC-type containing 23 [Source:HGNC Symbol;Acc:HGNC:32963]","synonyms":"FLJ45231","biotype":"lincRNA","ncbi_id":"645078","summary":null,"start":109303035,"end":109316135,"strand":1,"description":"zinc finger CCHC-type containing 23 [Source:HGNC Symbol;Acc:HGNC:32963]"}, {"versioned_ensembl_gene_id":"ENSG00000134900.11","gene_symbol":"TPP2","gene_name":"tripeptidyl peptidase 2 [Source:HGNC Symbol;Acc:HGNC:12016]","synonyms":"TPPII","biotype":"protein_coding","ncbi_id":"7174","summary":"This gene encodes a mammalian peptidase that, at neutral pH, removes tripeptides from the N terminus of longer peptides. The protein has a specialized function that is essential for some MHC class I antigen presentation. The protein is a high molecular mass serine exopeptidase; the amino acid sequence surrounding the serine residue at the active site is similar to the peptidases of the subtilisin class rather than the trypsin class. [provided by RefSeq, Jul 2008]","start":102597003,"end":102679958,"strand":1,"description":"tripeptidyl peptidase 2 [Source:HGNC Symbol;Acc:HGNC:12016]"}, {"versioned_ensembl_gene_id":"ENSG00000101596.14","gene_symbol":"SMCHD1","gene_name":"structural maintenance of chromosomes flexible hinge domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29090]","synonyms":"KIAA0650,FSHD2","biotype":"protein_coding","ncbi_id":"23347","summary":"This gene encodes a protein which contains a hinge region domain found in members of the SMC (structural maintenance of chromosomes) protein family. [provided by RefSeq, Dec 2011]","start":2655738,"end":2805017,"strand":1,"description":"structural maintenance of chromosomes flexible hinge domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29090]"}, {"versioned_ensembl_gene_id":"ENSG00000083535.15","gene_symbol":"PIBF1","gene_name":"progesterone immunomodulatory binding factor 1 [Source:HGNC Symbol;Acc:HGNC:23352]","synonyms":"CEP90,C13orf24","biotype":"protein_coding","ncbi_id":"10464","summary":"This gene encodes a protein that is induced by the steroid hormone progesterone and plays a role in the maintenance of pregnancy. The encoded protein regulates multiple facets of the immune system to promote normal pregnancy including cytokine synthesis, natural killer (NK) cell activity, and arachidonic acid metabolism. Low serum levels of this protein have been associated with spontaneous pre-term labor in humans. This protein may promote the proliferation, migration and invasion of glioma. [provided by RefSeq, Mar 2017]","start":72782059,"end":73016461,"strand":1,"description":"progesterone immunomodulatory binding factor 1 [Source:HGNC Symbol;Acc:HGNC:23352]"}, {"versioned_ensembl_gene_id":"ENSG00000198626.15","gene_symbol":"RYR2","gene_name":"ryanodine receptor 2 [Source:HGNC Symbol;Acc:HGNC:10484]","synonyms":"VTSIP,ARVD2,ARVC2","biotype":"protein_coding","ncbi_id":"6262","summary":"This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia. [provided by RefSeq, Jul 2008]","start":237042205,"end":237833988,"strand":1,"description":"ryanodine receptor 2 [Source:HGNC Symbol;Acc:HGNC:10484]"}, {"versioned_ensembl_gene_id":"ENSG00000282591.1","gene_symbol":"FAM138F","gene_name":"family with sequence similarity 138 member F [Source:HGNC Symbol;Acc:HGNC:33581]","synonyms":"F379","biotype":"lincRNA","ncbi_id":"641702","summary":null,"start":76163,"end":77686,"strand":-1,"description":"family with sequence similarity 138 member F [Source:HGNC Symbol;Acc:HGNC:33581]"}, {"versioned_ensembl_gene_id":"ENSG00000282807.3","gene_symbol":"AC008993.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71778,"end":72718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118855.18","gene_symbol":"MFSD1","gene_name":"major facilitator superfamily domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25874]","synonyms":"FLJ14153,UG0581B09","biotype":"protein_coding","ncbi_id":"64747","summary":null,"start":158732198,"end":158829719,"strand":1,"description":"major facilitator superfamily domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25874]"}, {"versioned_ensembl_gene_id":"ENSG00000272247.1","gene_symbol":"AC080013.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158801257,"end":158801935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253484.1","gene_symbol":"AC113145.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49817586,"end":49820944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256994.1","gene_symbol":"LINC02378","gene_name":"long intergenic non-protein coding RNA 2378 [Source:HGNC Symbol;Acc:HGNC:53301]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369678","summary":null,"start":17509353,"end":17589992,"strand":-1,"description":"long intergenic non-protein coding RNA 2378 [Source:HGNC Symbol;Acc:HGNC:53301]"}, {"versioned_ensembl_gene_id":"ENSG00000256389.1","gene_symbol":"AC087321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17589257,"end":17615463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121741.16","gene_symbol":"ZMYM2","gene_name":"zinc finger MYM-type containing 2 [Source:HGNC Symbol;Acc:HGNC:12989]","synonyms":"ZNF198,RAMP,MYM,FIM","biotype":"protein_coding","ncbi_id":"7750","summary":"The protein encoded by this gene is a zinc finger protein that may act as a transcription factor. The encoded protein may be part of a BHC histone deacetylase complex. Translocation of this gene with the fibroblast growth factor receptor-1 gene (FGFR1) results in a fusion gene, which may be a cause of stem cell leukemia lymphoma syndrome (SCLL). Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]","start":19958670,"end":20091829,"strand":1,"description":"zinc finger MYM-type containing 2 [Source:HGNC Symbol;Acc:HGNC:12989]"}, {"versioned_ensembl_gene_id":"ENSG00000157653.11","gene_symbol":"C9orf43","gene_name":"chromosome 9 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:23570]","synonyms":"MGC17358","biotype":"protein_coding","ncbi_id":"257169","summary":null,"start":113410054,"end":113429684,"strand":1,"description":"chromosome 9 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:23570]"}, {"versioned_ensembl_gene_id":"ENSG00000108786.10","gene_symbol":"HSD17B1","gene_name":"hydroxysteroid 17-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5210]","synonyms":"SDR28C1,MGC138140,HSD17,EDHB17,EDH17B2","biotype":"protein_coding","ncbi_id":"3292","summary":"This gene encodes a member of the 17beta-hydroxysteroid dehydrogenase family of short-chain dehydrogenases/reductases. It has a dual function in estrogen activation and androgen inactivation and plays a major role in establishing the estrogen E2 concentration gradient between serum and peripheral tissues. The encoded protein catalyzes the last step in estrogen activation, using NADPH to convert estrogens E1 and E2 and androgens like 4-androstenedione, to testosterone. It has an N-terminal short-chain dehydrogenase domain with a cofactor binding site, and a narrow, hydrophobic C-terminal domain with a steroid substrate binding site. This gene is expressed primarily in the placenta and ovarian granulosa cells, and to a lesser extent, in the endometrium, adipose tissue, and prostate. Polymorphisms in this gene have been linked to breast and prostate cancer. A pseudogene of this gene has been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":42549214,"end":42555213,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:5210]"}, {"versioned_ensembl_gene_id":"ENSG00000236273.1","gene_symbol":"BX927320.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31567594,"end":31568173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280239.1","gene_symbol":"AC011498.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4448810,"end":4450836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224478.1","gene_symbol":"AL356417.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159107791,"end":159116053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260260.1","gene_symbol":"SNHG19","gene_name":"small nucleolar RNA host gene 19 [Source:HGNC Symbol;Acc:HGNC:49574]","synonyms":"SNORD60HG","biotype":"lincRNA","ncbi_id":"100507303","summary":null,"start":2154797,"end":2155358,"strand":-1,"description":"small nucleolar RNA host gene 19 [Source:HGNC Symbol;Acc:HGNC:49574]"}, {"versioned_ensembl_gene_id":"ENSG00000119812.18","gene_symbol":"FAM98A","gene_name":"family with sequence similarity 98 member A [Source:HGNC Symbol;Acc:HGNC:24520]","synonyms":"DKFZP564F0522","biotype":"protein_coding","ncbi_id":"25940","summary":null,"start":33583658,"end":33599382,"strand":-1,"description":"family with sequence similarity 98 member A [Source:HGNC Symbol;Acc:HGNC:24520]"}, {"versioned_ensembl_gene_id":"ENSG00000156398.12","gene_symbol":"SFXN2","gene_name":"sideroflexin 2 [Source:HGNC Symbol;Acc:HGNC:16086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"118980","summary":null,"start":102714538,"end":102743492,"strand":1,"description":"sideroflexin 2 [Source:HGNC Symbol;Acc:HGNC:16086]"}, {"versioned_ensembl_gene_id":"ENSG00000279352.1","gene_symbol":"AC006557.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":14010054,"end":14010917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224599.1","gene_symbol":"BMS1P12","gene_name":"BMS1, ribosome biogenesis factor pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49157]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644684","summary":null,"start":65189995,"end":65193610,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49157]"}, {"versioned_ensembl_gene_id":"ENSG00000243779.1","gene_symbol":"AP001086.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13919603,"end":13919923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105392.15","gene_symbol":"CRX","gene_name":"cone-rod homeobox [Source:HGNC Symbol;Acc:HGNC:2383]","synonyms":"OTX3,LCA7,CRD,CORD2","biotype":"protein_coding","ncbi_id":"1406","summary":"The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":47819779,"end":47843330,"strand":1,"description":"cone-rod homeobox [Source:HGNC Symbol;Acc:HGNC:2383]"}, {"versioned_ensembl_gene_id":"ENSG00000109971.13","gene_symbol":"HSPA8","gene_name":"heat shock protein family A (Hsp70) member 8 [Source:HGNC Symbol;Acc:HGNC:5241]","synonyms":"HSPA10,HSP73,HSC71,HSC70","biotype":"protein_coding","ncbi_id":"3312","summary":"This gene encodes a member of the heat shock protein 70 family, which contains both heat-inducible and constitutively expressed members. This protein belongs to the latter group, which are also referred to as heat-shock cognate proteins. It functions as a chaperone, and binds to nascent polypeptides to facilitate correct folding. It also functions as an ATPase in the disassembly of clathrin-coated vesicles during transport of membrane components through the cell. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":123057489,"end":123063230,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 [Source:HGNC Symbol;Acc:HGNC:5241]"}, {"versioned_ensembl_gene_id":"ENSG00000111145.7","gene_symbol":"ELK3","gene_name":"ELK3, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3325]","synonyms":"SAP2,NET,ERP","biotype":"protein_coding","ncbi_id":"2004","summary":"This gene encodes a member of the ETS-domain transcription factor family and the ternary complex factor (TCF) subfamily. Proteins in this subfamily regulate transcription when recruited by serum response factor to bind to serum response elements. This protein is activated by signal-induced phosphorylation; studies in rodents suggest that it is a transcriptional inhibitor in the absence of Ras, but activates transcription when Ras is present. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":96194382,"end":96269835,"strand":1,"description":"ELK3, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3325]"}, {"versioned_ensembl_gene_id":"ENSG00000274351.1","gene_symbol":"AL137000.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49232874,"end":49234399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274460.1","gene_symbol":"AC092119.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":21950218,"end":21951708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102539.5","gene_symbol":"MLNR","gene_name":"motilin receptor [Source:HGNC Symbol;Acc:HGNC:4495]","synonyms":"GPR38","biotype":"protein_coding","ncbi_id":"2862","summary":"Motilin is a 22 amino acid peptide hormone expressed throughout the gastrointestinal (GI) tract. The protein encoded by this gene is a motilin receptor which is a member of the G-protein coupled receptor 1 family. This member is a multi-pass transmembrane protein, and is an important therapeutic target for the treatment of hypomotility disorders. [provided by RefSeq, Aug 2011]","start":49220338,"end":49222377,"strand":1,"description":"motilin receptor [Source:HGNC Symbol;Acc:HGNC:4495]"}, {"versioned_ensembl_gene_id":"ENSG00000257700.1","gene_symbol":"AC055716.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52692605,"end":52696788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112159.11","gene_symbol":"MDN1","gene_name":"midasin AAA ATPase 1 [Source:HGNC Symbol;Acc:HGNC:18302]","synonyms":"Rea1,KIAA0301","biotype":"protein_coding","ncbi_id":"23195","summary":null,"start":89642499,"end":89819723,"strand":-1,"description":"midasin AAA ATPase 1 [Source:HGNC Symbol;Acc:HGNC:18302]"}, {"versioned_ensembl_gene_id":"ENSG00000217653.1","gene_symbol":"AL353692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89814709,"end":89815463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228124.1","gene_symbol":"AL096678.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89673469,"end":89675783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136848.16","gene_symbol":"DAB2IP","gene_name":"DAB2 interacting protein [Source:HGNC Symbol;Acc:HGNC:17294]","synonyms":"KIAA1743,DIP1/2,AIP1,AF9Q34","biotype":"protein_coding","ncbi_id":"153090","summary":"DAB2IP is a Ras (MIM 190020) GTPase-activating protein (GAP) that acts as a tumor suppressor. The DAB2IP gene is inactivated by methylation in prostate and breast cancers (Yano et al., 2005 [PubMed 15386433]).[supplied by OMIM, May 2010]","start":121567057,"end":121785530,"strand":1,"description":"DAB2 interacting protein [Source:HGNC Symbol;Acc:HGNC:17294]"}, {"versioned_ensembl_gene_id":"ENSG00000220871.1","gene_symbol":"DNAJC19P6","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861449","summary":null,"start":89797598,"end":89797877,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45069]"}, {"versioned_ensembl_gene_id":"ENSG00000224730.1","gene_symbol":"LILRB1-AS1","gene_name":"LILRB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53114]","synonyms":"AC009892.10","biotype":"antisense_RNA","ncbi_id":"109729136","summary":null,"start":54635722,"end":54638892,"strand":-1,"description":"LILRB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53114]"}, {"versioned_ensembl_gene_id":"ENSG00000229854.1","gene_symbol":"AL357936.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121574891,"end":121576214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270039.1","gene_symbol":"AC025165.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57803838,"end":57804415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231738.10","gene_symbol":"TSPAN19","gene_name":"tetraspanin 19 [Source:HGNC Symbol;Acc:HGNC:31886]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144448","summary":null,"start":85014311,"end":85036277,"strand":-1,"description":"tetraspanin 19 [Source:HGNC Symbol;Acc:HGNC:31886]"}, {"versioned_ensembl_gene_id":"ENSG00000279138.1","gene_symbol":"AP002847.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":104478539,"end":104480783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119283.15","gene_symbol":"TRIM67","gene_name":"tripartite motif containing 67 [Source:HGNC Symbol;Acc:HGNC:31859]","synonyms":"TNL","biotype":"protein_coding","ncbi_id":"440730","summary":null,"start":231162112,"end":231221556,"strand":1,"description":"tripartite motif containing 67 [Source:HGNC Symbol;Acc:HGNC:31859]"}, {"versioned_ensembl_gene_id":"ENSG00000250897.2","gene_symbol":"HMGB3P15","gene_name":"high mobility group box 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39307]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644429","summary":null,"start":94195940,"end":94196513,"strand":-1,"description":"high mobility group box 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39307]"}, {"versioned_ensembl_gene_id":"ENSG00000168079.16","gene_symbol":"SCARA5","gene_name":"scavenger receptor class A member 5 [Source:HGNC Symbol;Acc:HGNC:28701]","synonyms":"NET33,MGC45780,FLJ23907","biotype":"protein_coding","ncbi_id":"286133","summary":null,"start":27869882,"end":27992727,"strand":-1,"description":"scavenger receptor class A member 5 [Source:HGNC Symbol;Acc:HGNC:28701]"}, {"versioned_ensembl_gene_id":"ENSG00000267978.5","gene_symbol":"MAGEA9B","gene_name":"MAGE family member A9B [Source:HGNC Symbol;Acc:HGNC:31909]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728269","summary":"MAGEA9B is a duplication of the MAGEA9 gene (MIM 300342) on chromosome Xq28. The 2 copies are separated by about 194 kb (Hartz, 2009).[supplied by OMIM, Mar 2009]","start":149581653,"end":149587453,"strand":-1,"description":"MAGE family member A9B [Source:HGNC Symbol;Acc:HGNC:31909]"}, {"versioned_ensembl_gene_id":"ENSG00000282542.1","gene_symbol":"AC008993.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68403,"end":69178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167671.11","gene_symbol":"UBXN6","gene_name":"UBX domain protein 6 [Source:HGNC Symbol;Acc:HGNC:14928]","synonyms":"UBXDC2,UBXD1","biotype":"protein_coding","ncbi_id":"80700","summary":null,"start":4444999,"end":4457822,"strand":-1,"description":"UBX domain protein 6 [Source:HGNC Symbol;Acc:HGNC:14928]"}, {"versioned_ensembl_gene_id":"ENSG00000267769.1","gene_symbol":"AC011498.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4454014,"end":4455286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278599.5","gene_symbol":"TBC1D3E","gene_name":"TBC1 domain family member 3E [Source:HGNC Symbol;Acc:HGNC:27071]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723859","summary":null,"start":38127951,"end":38138862,"strand":1,"description":"TBC1 domain family member 3E [Source:HGNC Symbol;Acc:HGNC:27071]"}, {"versioned_ensembl_gene_id":"ENSG00000267030.1","gene_symbol":"AC011498.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4447304,"end":4448217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248271.1","gene_symbol":"PGAM1P1","gene_name":"phosphoglycerate mutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130514","summary":null,"start":58161197,"end":58161752,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42448]"}, {"versioned_ensembl_gene_id":"ENSG00000248132.2","gene_symbol":"LINC02101","gene_name":"long intergenic non-protein coding RNA 2101 [Source:HGNC Symbol;Acc:HGNC:52956]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928569","summary":null,"start":58108082,"end":58122341,"strand":-1,"description":"long intergenic non-protein coding RNA 2101 [Source:HGNC Symbol;Acc:HGNC:52956]"}, {"versioned_ensembl_gene_id":"ENSG00000173928.2","gene_symbol":"SWSAP1","gene_name":"SWIM-type zinc finger 7 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:26638]","synonyms":"ZSWIM7AP1,SWS1AP1,FLJ35119,C19orf39","biotype":"protein_coding","ncbi_id":"126074","summary":null,"start":11374685,"end":11376951,"strand":1,"description":"SWIM-type zinc finger 7 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:26638]"}, {"versioned_ensembl_gene_id":"ENSG00000160563.13","gene_symbol":"MED27","gene_name":"mediator complex subunit 27 [Source:HGNC Symbol;Acc:HGNC:2377]","synonyms":"TRAP37,MED3,CRSP8,CRSP34","biotype":"protein_coding","ncbi_id":"9442","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2011]","start":131860107,"end":132079908,"strand":-1,"description":"mediator complex subunit 27 [Source:HGNC Symbol;Acc:HGNC:2377]"}, {"versioned_ensembl_gene_id":"ENSG00000243845.3","gene_symbol":"RN7SL30P","gene_name":"RNA, 7SL, cytoplasmic 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46046]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479235","summary":null,"start":125512902,"end":125513207,"strand":-1,"description":"RNA, 7SL, cytoplasmic 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:46046]"}, {"versioned_ensembl_gene_id":"ENSG00000202034.1","gene_symbol":"RNU6-399P","gene_name":"RNA, U6 small nuclear 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:47362]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481892","summary":null,"start":62545582,"end":62545679,"strand":-1,"description":"RNA, U6 small nuclear 399, pseudogene [Source:HGNC Symbol;Acc:HGNC:47362]"}, {"versioned_ensembl_gene_id":"ENSG00000274806.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":70194651,"end":70194830,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000167768.4","gene_symbol":"KRT1","gene_name":"keratin 1 [Source:HGNC Symbol;Acc:HGNC:6412]","synonyms":"KRT1A,EHK1","biotype":"protein_coding","ncbi_id":"3848","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the spinous and granular layers of the epidermis with family member KRT10 and mutations in these genes have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52674736,"end":52680407,"strand":-1,"description":"keratin 1 [Source:HGNC Symbol;Acc:HGNC:6412]"}, {"versioned_ensembl_gene_id":"ENSG00000261089.1","gene_symbol":"CDC37P2","gene_name":"cell division cycle 37 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35453]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647015","summary":null,"start":28413703,"end":28415018,"strand":1,"description":"cell division cycle 37 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35453]"}, {"versioned_ensembl_gene_id":"ENSG00000282491.1","gene_symbol":"AC243807.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45557439,"end":45574865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236687.1","gene_symbol":"AL160271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131816192,"end":131820988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213035.4","gene_symbol":"RPL23AP80","gene_name":"ribosomal protein L23a pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:36956]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390949","summary":null,"start":47794467,"end":47794890,"strand":-1,"description":"ribosomal protein L23a pseudogene 80 [Source:HGNC Symbol;Acc:HGNC:36956]"}, {"versioned_ensembl_gene_id":"ENSG00000228435.2","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"D6S53E,G4","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31640476,"end":31642950,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000237450.5","gene_symbol":"RPL23AP71","gene_name":"ribosomal protein L23a pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:36908]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644384","summary":null,"start":34485979,"end":34486447,"strand":1,"description":"ribosomal protein L23a pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:36908]"}, {"versioned_ensembl_gene_id":"ENSG00000239532.1","gene_symbol":"AC108022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37821361,"end":37821838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283653.1","gene_symbol":"AC091948.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148362777,"end":148372152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257408.2","gene_symbol":"AC092375.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21938865,"end":21944987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281842.2","gene_symbol":"MIR1291","gene_name":"microRNA 1291 [Source:HGNC Symbol;Acc:HGNC:35284]","synonyms":"MIRN1291,hsa-mir-1291","biotype":"miRNA","ncbi_id":"100302221","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48654444,"end":48654530,"strand":-1,"description":"microRNA 1291 [Source:HGNC Symbol;Acc:HGNC:35284]"}, {"versioned_ensembl_gene_id":"ENSG00000238420.1","gene_symbol":"RNU6-437P","gene_name":"RNA, U6 small nuclear 437, pseudogene [Source:HGNC Symbol;Acc:HGNC:47400]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479759","summary":null,"start":107930088,"end":107930182,"strand":1,"description":"RNA, U6 small nuclear 437, pseudogene [Source:HGNC Symbol;Acc:HGNC:47400]"}, {"versioned_ensembl_gene_id":"ENSG00000263540.1","gene_symbol":"MIR5582","gene_name":"microRNA 5582 [Source:HGNC Symbol;Acc:HGNC:43461]","synonyms":"hsa-mir-5582","biotype":"miRNA","ncbi_id":"100847020","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46753125,"end":46753192,"strand":-1,"description":"microRNA 5582 [Source:HGNC Symbol;Acc:HGNC:43461]"}, {"versioned_ensembl_gene_id":"ENSG00000252350.1","gene_symbol":"RPPH1-3P","gene_name":"ribonuclease P RNA component H1, 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:47030]","synonyms":null,"biotype":"ribozyme","ncbi_id":"106479602","summary":null,"start":156986372,"end":156986693,"strand":-1,"description":"ribonuclease P RNA component H1, 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:47030]"}, {"versioned_ensembl_gene_id":"ENSG00000264384.2","gene_symbol":"RN7SL431P","gene_name":"RNA, 7SL, cytoplasmic 431, pseudogene [Source:HGNC Symbol;Acc:HGNC:46447]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106866913","summary":null,"start":154166245,"end":154166549,"strand":-1,"description":"RNA, 7SL, cytoplasmic 431, pseudogene [Source:HGNC Symbol;Acc:HGNC:46447]"}, {"versioned_ensembl_gene_id":"ENSG00000281771.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67631019,"end":67631127,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272469.2","gene_symbol":"RN7SL760P","gene_name":"RNA, 7SL, cytoplasmic 760, pseudogene [Source:HGNC Symbol;Acc:HGNC:46776]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481129","summary":null,"start":73833773,"end":73834042,"strand":-1,"description":"RNA, 7SL, cytoplasmic 760, pseudogene [Source:HGNC Symbol;Acc:HGNC:46776]"}, {"versioned_ensembl_gene_id":"ENSG00000283876.1","gene_symbol":"MIR4260","gene_name":"microRNA 4260 [Source:HGNC Symbol;Acc:HGNC:38179]","synonyms":"hsa-mir-4260","biotype":"miRNA","ncbi_id":"100422894","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":209623444,"end":209623510,"strand":-1,"description":"microRNA 4260 [Source:HGNC Symbol;Acc:HGNC:38179]"}, {"versioned_ensembl_gene_id":"ENSG00000210181.1","gene_symbol":"RNU6ATAC4P","gene_name":"RNA, U6atac small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:34094]","synonyms":null,"biotype":"snRNA","ncbi_id":"100151687","summary":null,"start":36968191,"end":36968316,"strand":-1,"description":"RNA, U6atac small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:34094]"}, {"versioned_ensembl_gene_id":"ENSG00000252774.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":64342539,"end":64342698,"strand":1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000241144.3","gene_symbol":"RN7SL728P","gene_name":"RNA, 7SL, cytoplasmic 728, pseudogene [Source:HGNC Symbol;Acc:HGNC:46744]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481857","summary":null,"start":102348392,"end":102348691,"strand":-1,"description":"RNA, 7SL, cytoplasmic 728, pseudogene [Source:HGNC Symbol;Acc:HGNC:46744]"}, {"versioned_ensembl_gene_id":"ENSG00000202318.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6234345,"end":6234455,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276153.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38031608,"end":38031709,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277614.1","gene_symbol":"SCG5","gene_name":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]","synonyms":"SGNE1,7B2,SgV,SGNE1,7B2,SgV","biotype":"protein_coding","ncbi_id":"6447","summary":"This gene encodes a secreted chaperone protein that prevents the aggregation of other secreted proteins, including proteins that are associated with neurodegenerative and metabolic disease. The encoded protein may be best known for its role in the trafficking and activation of prohormone convertase PC2 (encoded by Gene ID: 5126). Phosphorylation of the encoded protein has been shown to have an inhibitory effect on its chaperone function. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32721966,"end":32777405,"strand":1,"description":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]"}, {"versioned_ensembl_gene_id":"ENSG00000201465.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":138187998,"end":138188129,"strand":-1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000222328.1","gene_symbol":"RNU2-2P","gene_name":"RNA, U2 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:10152]","synonyms":"U2,RNU2B,RNU2-2","biotype":"snRNA","ncbi_id":"26855","summary":null,"start":62841619,"end":62841809,"strand":-1,"description":"RNA, U2 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:10152]"}, {"versioned_ensembl_gene_id":"ENSG00000206598.1","gene_symbol":"RNU6-1286P","gene_name":"RNA, U6 small nuclear 1286, pseudogene [Source:HGNC Symbol;Acc:HGNC:48249]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481586","summary":null,"start":121354354,"end":121354460,"strand":1,"description":"RNA, U6 small nuclear 1286, pseudogene [Source:HGNC Symbol;Acc:HGNC:48249]"}, {"versioned_ensembl_gene_id":"ENSG00000199806.1","gene_symbol":"RNA5SP491","gene_name":"RNA, 5S ribosomal pseudogene 491 [Source:HGNC Symbol;Acc:HGNC:43391]","synonyms":"RN5S491","biotype":"rRNA","ncbi_id":"100873733","summary":null,"start":36851911,"end":36852028,"strand":1,"description":"RNA, 5S ribosomal pseudogene 491 [Source:HGNC Symbol;Acc:HGNC:43391]"}, {"versioned_ensembl_gene_id":"ENSG00000212608.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":53387713,"end":53387836,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000251965.1","gene_symbol":"RNA5SP208","gene_name":"RNA, 5S ribosomal pseudogene 208 [Source:HGNC Symbol;Acc:HGNC:43108]","synonyms":"RN5S208","biotype":"rRNA","ncbi_id":"100873468","summary":null,"start":67467231,"end":67467308,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 208 [Source:HGNC Symbol;Acc:HGNC:43108]"}, {"versioned_ensembl_gene_id":"ENSG00000244230.3","gene_symbol":"RN7SL151P","gene_name":"RNA, 7SL, cytoplasmic 151, pseudogene [Source:HGNC Symbol;Acc:HGNC:46167]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107075319","summary":null,"start":21699314,"end":21699596,"strand":1,"description":"RNA, 7SL, cytoplasmic 151, pseudogene [Source:HGNC Symbol;Acc:HGNC:46167]"}, {"versioned_ensembl_gene_id":"ENSG00000274091.1","gene_symbol":"SNORD1C","gene_name":"small nucleolar RNA, C/D box 1C [Source:HGNC Symbol;Acc:HGNC:32677]","synonyms":"snR38C,R38C","biotype":"snoRNA","ncbi_id":"677850","summary":null,"start":76558791,"end":76558868,"strand":1,"description":"small nucleolar RNA, C/D box 1C [Source:HGNC Symbol;Acc:HGNC:32677]"}, {"versioned_ensembl_gene_id":"ENSG00000280963.2","gene_symbol":"SERTAD4-AS1","gene_name":"SERTAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32019]","synonyms":"C1orf133","biotype":"antisense_RNA","ncbi_id":"574036","summary":null,"start":210231456,"end":210234047,"strand":-1,"description":"SERTAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32019]"}, {"versioned_ensembl_gene_id":"ENSG00000273554.4","gene_symbol":"AC136616.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1139577,"end":1147868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241226.3","gene_symbol":"RN7SL836P","gene_name":"RNA, 7SL, cytoplasmic 836, pseudogene [Source:HGNC Symbol;Acc:HGNC:46852]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481149","summary":null,"start":45651510,"end":45651805,"strand":1,"description":"RNA, 7SL, cytoplasmic 836, pseudogene [Source:HGNC Symbol;Acc:HGNC:46852]"}, {"versioned_ensembl_gene_id":"ENSG00000283337.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":102868421,"end":102868519,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000281430.1","gene_symbol":"LCN1P2","gene_name":"lipocalin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23680]","synonyms":"LCN1L2,bA244N20.11","biotype":"unprocessed_pseudogene","ncbi_id":"653163","summary":null,"start":133317942,"end":133318617,"strand":1,"description":"lipocalin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23680]"}, {"versioned_ensembl_gene_id":"ENSG00000238317.2","gene_symbol":"SNORD11","gene_name":"small nucleolar RNA, C/D box 11 [Source:HGNC Symbol;Acc:HGNC:32707]","synonyms":"HBII-95","biotype":"snoRNA","ncbi_id":"692058","summary":null,"start":202293051,"end":202293134,"strand":1,"description":"small nucleolar RNA, C/D box 11 [Source:HGNC Symbol;Acc:HGNC:32707]"}, {"versioned_ensembl_gene_id":"ENSG00000251985.1","gene_symbol":"RNU6-1161P","gene_name":"RNA, U6 small nuclear 1161, pseudogene [Source:HGNC Symbol;Acc:HGNC:48124]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480077","summary":null,"start":45624531,"end":45624632,"strand":-1,"description":"RNA, U6 small nuclear 1161, pseudogene [Source:HGNC Symbol;Acc:HGNC:48124]"}, {"versioned_ensembl_gene_id":"ENSG00000207757.1","gene_symbol":"MIR93","gene_name":"microRNA 93 [Source:HGNC Symbol;Acc:HGNC:31645]","synonyms":"MIRN93,hsa-mir-93","biotype":"miRNA","ncbi_id":"407050","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100093768,"end":100093847,"strand":-1,"description":"microRNA 93 [Source:HGNC Symbol;Acc:HGNC:31645]"}, {"versioned_ensembl_gene_id":"ENSG00000283616.1","gene_symbol":"MIR5683","gene_name":"microRNA 5683 [Source:HGNC Symbol;Acc:HGNC:43453]","synonyms":"hsa-mir-5683","biotype":"miRNA","ncbi_id":"100847034","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6169334,"end":6169409,"strand":1,"description":"microRNA 5683 [Source:HGNC Symbol;Acc:HGNC:43453]"}, {"versioned_ensembl_gene_id":"ENSG00000207739.1","gene_symbol":"MIR218-2","gene_name":"microRNA 218-2 [Source:HGNC Symbol;Acc:HGNC:31596]","synonyms":"MIRN218-2,hsa-mir-218-2","biotype":"miRNA","ncbi_id":"407001","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168768146,"end":168768255,"strand":-1,"description":"microRNA 218-2 [Source:HGNC Symbol;Acc:HGNC:31596]"}, {"versioned_ensembl_gene_id":"ENSG00000201036.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100979002,"end":100979090,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000199884.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":152284350,"end":152284460,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274626.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000272543.1","gene_symbol":"MIR4787","gene_name":"microRNA 4787 [Source:HGNC Symbol;Acc:HGNC:41653]","synonyms":"hsa-mir-4787","biotype":"miRNA","ncbi_id":"100616138","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50675080,"end":50675163,"strand":1,"description":"microRNA 4787 [Source:HGNC Symbol;Acc:HGNC:41653]"}, {"versioned_ensembl_gene_id":"ENSG00000266012.1","gene_symbol":"MIR4764","gene_name":"microRNA 4764 [Source:HGNC Symbol;Acc:HGNC:41714]","synonyms":"hsa-mir-4764","biotype":"miRNA","ncbi_id":"100616295","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33436582,"end":33436669,"strand":-1,"description":"microRNA 4764 [Source:HGNC Symbol;Acc:HGNC:41714]"}, {"versioned_ensembl_gene_id":"ENSG00000212586.1","gene_symbol":"SNORA8","gene_name":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]","synonyms":"ACA8","biotype":"snoRNA","ncbi_id":"654320","summary":null,"start":38822307,"end":38822404,"strand":-1,"description":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]"}, {"versioned_ensembl_gene_id":"ENSG00000264090.1","gene_symbol":"MIR4666B","gene_name":"microRNA 4666b [Source:HGNC Symbol;Acc:HGNC:43486]","synonyms":"hsa-mir-4666b","biotype":"miRNA","ncbi_id":"100847047","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29574278,"end":29574358,"strand":1,"description":"microRNA 4666b [Source:HGNC Symbol;Acc:HGNC:43486]"}, {"versioned_ensembl_gene_id":"ENSG00000265284.1","gene_symbol":"MIR4770","gene_name":"microRNA 4770 [Source:HGNC Symbol;Acc:HGNC:41542]","synonyms":"hsa-mir-4770","biotype":"miRNA","ncbi_id":"100616373","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6383906,"end":6383963,"strand":-1,"description":"microRNA 4770 [Source:HGNC Symbol;Acc:HGNC:41542]"}, {"versioned_ensembl_gene_id":"ENSG00000283710.1","gene_symbol":"MIR1204","gene_name":"microRNA 1204 [Source:HGNC Symbol;Acc:HGNC:37059]","synonyms":"hsa-mir-1204","biotype":"miRNA","ncbi_id":"100302185","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127795962,"end":127796028,"strand":1,"description":"microRNA 1204 [Source:HGNC Symbol;Acc:HGNC:37059]"}, {"versioned_ensembl_gene_id":"ENSG00000206811.1","gene_symbol":"SNORA10","gene_name":"small nucleolar RNA, H/ACA box 10 [Source:HGNC Symbol;Acc:HGNC:32598]","synonyms":"SNORA10A,ACA10","biotype":"snoRNA","ncbi_id":"574042","summary":null,"start":1962334,"end":1962466,"strand":-1,"description":"small nucleolar RNA, H/ACA box 10 [Source:HGNC Symbol;Acc:HGNC:32598]"}, {"versioned_ensembl_gene_id":"ENSG00000275856.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30058115,"end":30058190,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000222792.1","gene_symbol":"RNU6-860P","gene_name":"RNA, U6 small nuclear 860, pseudogene [Source:HGNC Symbol;Acc:HGNC:47823]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479946","summary":null,"start":198196746,"end":198196849,"strand":1,"description":"RNA, U6 small nuclear 860, pseudogene [Source:HGNC Symbol;Acc:HGNC:47823]"}, {"versioned_ensembl_gene_id":"ENSG00000280496.1","gene_symbol":"SNORA17B","gene_name":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]","synonyms":"SNORA43,ACA43,SNORA43,ACA43","biotype":"snoRNA","ncbi_id":"677824","summary":null,"start":136726104,"end":136726239,"strand":-1,"description":"small nucleolar RNA, H/ACA box 17B [Source:HGNC Symbol;Acc:HGNC:32636]"}, {"versioned_ensembl_gene_id":"ENSG00000221421.1","gene_symbol":"MIR1283-1","gene_name":"microRNA 1283-1 [Source:HGNC Symbol;Acc:HGNC:35255]","synonyms":"MIRN1283-1,hsa-mir-1283-1","biotype":"miRNA","ncbi_id":"100302265","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53688481,"end":53688567,"strand":1,"description":"microRNA 1283-1 [Source:HGNC Symbol;Acc:HGNC:35255]"}, {"versioned_ensembl_gene_id":"ENSG00000207093.1","gene_symbol":"SNORD116-8","gene_name":"small nucleolar RNA, C/D box 116-8 [Source:HGNC Symbol;Acc:HGNC:33074]","synonyms":"HBII-85-8","biotype":"snoRNA","ncbi_id":"100033420","summary":null,"start":25070432,"end":25070526,"strand":1,"description":"small nucleolar RNA, C/D box 116-8 [Source:HGNC Symbol;Acc:HGNC:33074]"}, {"versioned_ensembl_gene_id":"ENSG00000274206.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96938923,"end":96939203,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283575.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":180758722,"end":180758817,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000264358.1","gene_symbol":"MIR3122","gene_name":"microRNA 3122 [Source:HGNC Symbol;Acc:HGNC:38320]","synonyms":"hsa-mir-3122","biotype":"miRNA","ncbi_id":"100422947","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":212077613,"end":212077685,"strand":1,"description":"microRNA 3122 [Source:HGNC Symbol;Acc:HGNC:38320]"}, {"versioned_ensembl_gene_id":"ENSG00000284163.1","gene_symbol":"MIR3620","gene_name":"microRNA 3620 [Source:HGNC Symbol;Acc:HGNC:38917]","synonyms":"hsa-mir-3620","biotype":"miRNA","ncbi_id":"100500810","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":228097263,"end":228097341,"strand":1,"description":"microRNA 3620 [Source:HGNC Symbol;Acc:HGNC:38917]"}, {"versioned_ensembl_gene_id":"ENSG00000253088.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":152402780,"end":152402893,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207738.1","gene_symbol":"MIR520C","gene_name":"microRNA 520c [Source:HGNC Symbol;Acc:HGNC:32108]","synonyms":"MIRN520C,hsa-mir-520c","biotype":"miRNA","ncbi_id":"574476","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53707453,"end":53707539,"strand":1,"description":"microRNA 520c [Source:HGNC Symbol;Acc:HGNC:32108]"}, {"versioned_ensembl_gene_id":"ENSG00000274747.1","gene_symbol":"RN7SL627P","gene_name":"RNA, 7SL, cytoplasmic 627, pseudogene [Source:HGNC Symbol;Acc:HGNC:46643]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481093","summary":null,"start":18840618,"end":18840920,"strand":1,"description":"RNA, 7SL, cytoplasmic 627, pseudogene [Source:HGNC Symbol;Acc:HGNC:46643]"}, {"versioned_ensembl_gene_id":"ENSG00000276145.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000265991.1","gene_symbol":"MIR4519","gene_name":"microRNA 4519 [Source:HGNC Symbol;Acc:HGNC:41544]","synonyms":"hsa-mir-4519","biotype":"miRNA","ncbi_id":"100616231","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30875266,"end":30875323,"strand":-1,"description":"microRNA 4519 [Source:HGNC Symbol;Acc:HGNC:41544]"}, {"versioned_ensembl_gene_id":"ENSG00000223220.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":70780914,"end":70781008,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264866.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28977461,"end":28977759,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207366.1","gene_symbol":"RNU6-297P","gene_name":"RNA, U6 small nuclear 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:47260]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479699","summary":null,"start":48341226,"end":48341332,"strand":-1,"description":"RNA, U6 small nuclear 297, pseudogene [Source:HGNC Symbol;Acc:HGNC:47260]"}, {"versioned_ensembl_gene_id":"ENSG00000264850.1","gene_symbol":"MIR4310","gene_name":"microRNA 4310 [Source:HGNC Symbol;Acc:HGNC:38383]","synonyms":"hsa-mir-4310","biotype":"miRNA","ncbi_id":"100423013","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41866495,"end":41866551,"strand":-1,"description":"microRNA 4310 [Source:HGNC Symbol;Acc:HGNC:38383]"}, {"versioned_ensembl_gene_id":"ENSG00000263693.1","gene_symbol":"MIR3161","gene_name":"microRNA 3161 [Source:HGNC Symbol;Acc:HGNC:38285]","synonyms":"hsa-mir-3161","biotype":"miRNA","ncbi_id":"100423000","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48096782,"end":48096858,"strand":1,"description":"microRNA 3161 [Source:HGNC Symbol;Acc:HGNC:38285]"}, {"versioned_ensembl_gene_id":"ENSG00000274175.1","gene_symbol":"AC133551.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17234,"end":19833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207776.1","gene_symbol":"MIR551A","gene_name":"microRNA 551a [Source:HGNC Symbol;Acc:HGNC:32806]","synonyms":"MIRN551A,hsa-mir-551a","biotype":"miRNA","ncbi_id":"693135","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3560695,"end":3560790,"strand":-1,"description":"microRNA 551a [Source:HGNC Symbol;Acc:HGNC:32806]"}, {"versioned_ensembl_gene_id":"ENSG00000251935.1","gene_symbol":"RN7SKP179","gene_name":"RNA, 7SK small nuclear pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:45903]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481815","summary":null,"start":190553264,"end":190553480,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 179 [Source:HGNC Symbol;Acc:HGNC:45903]"}, {"versioned_ensembl_gene_id":"ENSG00000201300.1","gene_symbol":"SNORD115-27","gene_name":"small nucleolar RNA, C/D box 115-27 [Source:HGNC Symbol;Acc:HGNC:33046]","synonyms":"HBII-52-27","biotype":"snoRNA","ncbi_id":"100036564","summary":null,"start":25220497,"end":25220578,"strand":1,"description":"small nucleolar RNA, C/D box 115-27 [Source:HGNC Symbol;Acc:HGNC:33046]"}, {"versioned_ensembl_gene_id":"ENSG00000199286.1","gene_symbol":"RNU6-1094P","gene_name":"RNA, U6 small nuclear 1094, pseudogene [Source:HGNC Symbol;Acc:HGNC:48057]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480047","summary":null,"start":96608814,"end":96608917,"strand":-1,"description":"RNA, U6 small nuclear 1094, pseudogene [Source:HGNC Symbol;Acc:HGNC:48057]"}, {"versioned_ensembl_gene_id":"ENSG00000242860.3","gene_symbol":"RN7SL180P","gene_name":"RNA, 7SL, cytoplasmic 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:46196]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480970","summary":null,"start":62072448,"end":62072741,"strand":1,"description":"RNA, 7SL, cytoplasmic 180, pseudogene [Source:HGNC Symbol;Acc:HGNC:46196]"}, {"versioned_ensembl_gene_id":"ENSG00000278421.1","gene_symbol":"FTX_1","gene_name":"FTX transcript, XIST regulator conserved region 1 [Source:RFAM;Acc:RF02119]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74274341,"end":74274411,"strand":1,"description":"FTX transcript, XIST regulator conserved region 1 [Source:RFAM;Acc:RF02119]"}, {"versioned_ensembl_gene_id":"ENSG00000206964.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55286018,"end":55286128,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252214.1","gene_symbol":"RNU6-542P","gene_name":"RNA, U6 small nuclear 542, pseudogene [Source:HGNC Symbol;Acc:HGNC:47505]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480588","summary":null,"start":74319399,"end":74319501,"strand":1,"description":"RNA, U6 small nuclear 542, pseudogene [Source:HGNC Symbol;Acc:HGNC:47505]"}, {"versioned_ensembl_gene_id":"ENSG00000206625.1","gene_symbol":"RNU6-1","gene_name":"RNA, U6 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10227]","synonyms":"U6-1,U6,RNU6A","biotype":"snRNA","ncbi_id":"26827","summary":null,"start":67839939,"end":67840045,"strand":-1,"description":"RNA, U6 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10227]"}, {"versioned_ensembl_gene_id":"ENSG00000275128.1","gene_symbol":"RN7SL203P","gene_name":"RNA, 7SL, cytoplasmic 203, pseudogene [Source:HGNC Symbol;Acc:HGNC:46219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479296","summary":null,"start":70480192,"end":70480487,"strand":-1,"description":"RNA, 7SL, cytoplasmic 203, pseudogene [Source:HGNC Symbol;Acc:HGNC:46219]"}, {"versioned_ensembl_gene_id":"ENSG00000266794.2","gene_symbol":"RN7SL7P","gene_name":"RNA, 7SL, cytoplasmic 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:10042]","synonyms":"RN7SLP4,RN7SL27P,7L23","biotype":"misc_RNA","ncbi_id":"6033","summary":null,"start":92971002,"end":92971299,"strand":-1,"description":"RNA, 7SL, cytoplasmic 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:10042]"}, {"versioned_ensembl_gene_id":"ENSG00000200338.1","gene_symbol":"RNU1-49P","gene_name":"RNA, U1 small nuclear 49, pseudogene [Source:HGNC 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[provided by RefSeq, Sep 2009]","start":20528275,"end":20528384,"strand":1,"description":"microRNA 218-1 [Source:HGNC Symbol;Acc:HGNC:31595]"}, {"versioned_ensembl_gene_id":"ENSG00000240294.2","gene_symbol":"RN7SKP241","gene_name":"RNA, 7SK small nuclear pseudogene 241 [Source:HGNC Symbol;Acc:HGNC:45965]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107063536","summary":null,"start":24908522,"end":24908812,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 241 [Source:HGNC Symbol;Acc:HGNC:45965]"}, {"versioned_ensembl_gene_id":"ENSG00000202566.4","gene_symbol":"MIR421","gene_name":"microRNA 421 [Source:HGNC Symbol;Acc:HGNC:32793]","synonyms":"MIRN421,hsa-mir-421","biotype":"miRNA","ncbi_id":"693122","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74218377,"end":74218461,"strand":-1,"description":"microRNA 421 [Source:HGNC Symbol;Acc:HGNC:32793]"}, {"versioned_ensembl_gene_id":"ENSG00000207192.1","gene_symbol":"RNU6-649P","gene_name":"RNA, U6 small nuclear 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:47612]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479854","summary":null,"start":4945277,"end":4945383,"strand":1,"description":"RNA, U6 small nuclear 649, pseudogene [Source:HGNC Symbol;Acc:HGNC:47612]"}, {"versioned_ensembl_gene_id":"ENSG00000252993.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":92076242,"end":92076365,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000283523.1","gene_symbol":"MIR3926-2","gene_name":"microRNA 3926-2 [Source:HGNC Symbol;Acc:HGNC:38883]","synonyms":"hsa-mir-3926-2","biotype":"miRNA","ncbi_id":"100500838","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12727237,"end":12727299,"strand":1,"description":"microRNA 3926-2 [Source:HGNC Symbol;Acc:HGNC:38883]"}, {"versioned_ensembl_gene_id":"ENSG00000222800.1","gene_symbol":"RNU2-62P","gene_name":"RNA, U2 small nuclear 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:48555]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480224","summary":null,"start":27109790,"end":27109980,"strand":-1,"description":"RNA, U2 small nuclear 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:48555]"}, {"versioned_ensembl_gene_id":"ENSG00000252200.1","gene_symbol":"snoZ6","gene_name":"Z6 small nucleolar RNA [Source:RFAM;Acc:RF00285]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":44725984,"end":44726058,"strand":-1,"description":"Z6 small nucleolar RNA [Source:RFAM;Acc:RF00285]"}, {"versioned_ensembl_gene_id":"ENSG00000265903.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30854117,"end":30854419,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000264536.1","gene_symbol":"MIR5706","gene_name":"microRNA 5706 [Source:HGNC Symbol;Acc:HGNC:43500]","synonyms":"hsa-mir-5706","biotype":"miRNA","ncbi_id":"100847085","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119154637,"end":119154716,"strand":1,"description":"microRNA 5706 [Source:HGNC Symbol;Acc:HGNC:43500]"}, {"versioned_ensembl_gene_id":"ENSG00000221265.1","gene_symbol":"MIR1255A","gene_name":"microRNA 1255a [Source:HGNC Symbol;Acc:HGNC:35320]","synonyms":"MIRN1255A,hsa-mir-1255a","biotype":"miRNA","ncbi_id":"100302193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101330302,"end":101330414,"strand":-1,"description":"microRNA 1255a [Source:HGNC Symbol;Acc:HGNC:35320]"}, {"versioned_ensembl_gene_id":"ENSG00000206947.1","gene_symbol":"SNORA20B","gene_name":"small nucleolar RNA, H/ACA box 20B [Source:HGNC Symbol;Acc:HGNC:52194]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616963","summary":null,"start":39329003,"end":39329134,"strand":-1,"description":"small nucleolar RNA, H/ACA box 20B [Source:HGNC Symbol;Acc:HGNC:52194]"}, {"versioned_ensembl_gene_id":"ENSG00000274552.1","gene_symbol":"MIR6889","gene_name":"microRNA 6889 [Source:HGNC Symbol;Acc:HGNC:50014]","synonyms":"hsa-mir-6889","biotype":"miRNA","ncbi_id":"102466758","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41252992,"end":41253050,"strand":-1,"description":"microRNA 6889 [Source:HGNC Symbol;Acc:HGNC:50014]"}, {"versioned_ensembl_gene_id":"ENSG00000201658.1","gene_symbol":"RNU6-283P","gene_name":"RNA, U6 small nuclear 283, pseudogene [Source:HGNC Symbol;Acc:HGNC:47246]","synonyms":"RNU6-683P","biotype":"snRNA","ncbi_id":"106479692","summary":null,"start":31370134,"end":31370240,"strand":1,"description":"RNA, U6 small nuclear 283, pseudogene [Source:HGNC Symbol;Acc:HGNC:47246]"}, {"versioned_ensembl_gene_id":"ENSG00000280636.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":179934401,"end":179934538,"strand":-1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000212282.1","gene_symbol":"RNU6-578P","gene_name":"RNA, U6 small nuclear 578, pseudogene [Source:HGNC Symbol;Acc:HGNC:47541]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481904","summary":null,"start":12312588,"end":12312690,"strand":1,"description":"RNA, U6 small nuclear 578, pseudogene [Source:HGNC Symbol;Acc:HGNC:47541]"}, {"versioned_ensembl_gene_id":"ENSG00000263512.1","gene_symbol":"MIR4311","gene_name":"microRNA 4311 [Source:HGNC Symbol;Acc:HGNC:38207]","synonyms":"hsa-mir-4311","biotype":"miRNA","ncbi_id":"100422905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66040233,"end":66040332,"strand":1,"description":"microRNA 4311 [Source:HGNC Symbol;Acc:HGNC:38207]"}, {"versioned_ensembl_gene_id":"ENSG00000263453.1","gene_symbol":"MIR4532","gene_name":"microRNA 4532 [Source:HGNC Symbol;Acc:HGNC:41869]","synonyms":"hsa-mir-4532","biotype":"miRNA","ncbi_id":"100616353","summary":"This record was withdrawn by miRBase.","start":57895394,"end":57895444,"strand":1,"description":"microRNA 4532 [Source:HGNC Symbol;Acc:HGNC:41869]"}, {"versioned_ensembl_gene_id":"ENSG00000212303.1","gene_symbol":"RNU6-1154P","gene_name":"RNA, U6 small nuclear 1154, pseudogene [Source:HGNC Symbol;Acc:HGNC:48117]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480074","summary":null,"start":135665599,"end":135665702,"strand":-1,"description":"RNA, U6 small nuclear 1154, pseudogene [Source:HGNC Symbol;Acc:HGNC:48117]"}, {"versioned_ensembl_gene_id":"ENSG00000264793.1","gene_symbol":"MIR4771-1","gene_name":"microRNA 4771-1 [Source:HGNC Symbol;Acc:HGNC:41901]","synonyms":"hsa-mir-4771-1","biotype":"miRNA","ncbi_id":"100616370","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87194786,"end":87194859,"strand":1,"description":"microRNA 4771-1 [Source:HGNC Symbol;Acc:HGNC:41901]"}, {"versioned_ensembl_gene_id":"ENSG00000207712.1","gene_symbol":"MIR627","gene_name":"microRNA 627 [Source:HGNC Symbol;Acc:HGNC:32883]","synonyms":"MIRN627,hsa-mir-627","biotype":"miRNA","ncbi_id":"693212","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42199570,"end":42199666,"strand":-1,"description":"microRNA 627 [Source:HGNC Symbol;Acc:HGNC:32883]"}, {"versioned_ensembl_gene_id":"ENSG00000202517.1","gene_symbol":"SNORA64","gene_name":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]","synonyms":"RNU64,U64","biotype":"snoRNA","ncbi_id":"26784","summary":null,"start":40238608,"end":40238741,"strand":1,"description":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]"}, {"versioned_ensembl_gene_id":"ENSG00000199077.3","gene_symbol":"MIR129-2","gene_name":"microRNA 129-2 [Source:HGNC Symbol;Acc:HGNC:31513]","synonyms":"MIRN129-2,hsa-mir-129-2","biotype":"miRNA","ncbi_id":"406918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43581394,"end":43581483,"strand":1,"description":"microRNA 129-2 [Source:HGNC Symbol;Acc:HGNC:31513]"}, {"versioned_ensembl_gene_id":"ENSG00000277521.1","gene_symbol":"MIR8078","gene_name":"microRNA 8078 [Source:HGNC Symbol;Acc:HGNC:50102]","synonyms":"hsa-mir-8078","biotype":"miRNA","ncbi_id":"102466878","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112256,"end":112339,"strand":-1,"description":"microRNA 8078 [Source:HGNC Symbol;Acc:HGNC:50102]"}, {"versioned_ensembl_gene_id":"ENSG00000251850.1","gene_symbol":"RNA5SP96","gene_name":"RNA, 5S ribosomal pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:42894]","synonyms":"RN5S96","biotype":"rRNA","ncbi_id":"100873329","summary":null,"start":69181897,"end":69182003,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:42894]"}, {"versioned_ensembl_gene_id":"ENSG00000206777.1","gene_symbol":"RNU6-637P","gene_name":"RNA, U6 small nuclear 637, pseudogene [Source:HGNC Symbol;Acc:HGNC:47600]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479848","summary":null,"start":169720187,"end":169720293,"strand":-1,"description":"RNA, U6 small nuclear 637, pseudogene [Source:HGNC Symbol;Acc:HGNC:47600]"}, {"versioned_ensembl_gene_id":"ENSG00000266327.1","gene_symbol":"MIR4503","gene_name":"microRNA 4503 [Source:HGNC Symbol;Acc:HGNC:41675]","synonyms":"hsa-mir-4503","biotype":"miRNA","ncbi_id":"100616280","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36952309,"end":36952391,"strand":-1,"description":"microRNA 4503 [Source:HGNC Symbol;Acc:HGNC:41675]"}, {"versioned_ensembl_gene_id":"ENSG00000280454.1","gene_symbol":"AC007347.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":54114697,"end":54114878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283326.1","gene_symbol":"MIR6860","gene_name":"microRNA 6860 [Source:HGNC Symbol;Acc:HGNC:50086]","synonyms":"hsa-mir-6860","biotype":"miRNA","ncbi_id":"102465518","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67045643,"end":67045708,"strand":1,"description":"microRNA 6860 [Source:HGNC Symbol;Acc:HGNC:50086]"}, {"versioned_ensembl_gene_id":"ENSG00000284155.1","gene_symbol":"MIR194-2","gene_name":"microRNA 194-2 [Source:HGNC Symbol;Acc:HGNC:31565]","synonyms":"MIRN194-2,hsa-mir-194-2","biotype":"miRNA","ncbi_id":"406970","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64891355,"end":64891439,"strand":-1,"description":"microRNA 194-2 [Source:HGNC Symbol;Acc:HGNC:31565]"}, {"versioned_ensembl_gene_id":"ENSG00000283676.1","gene_symbol":"MIR5087","gene_name":"microRNA 5087 [Source:HGNC Symbol;Acc:HGNC:43480]","synonyms":"hsa-mir-5087","biotype":"miRNA","ncbi_id":"100847044","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":148334479,"end":148334554,"strand":-1,"description":"microRNA 5087 [Source:HGNC Symbol;Acc:HGNC:43480]"}, {"versioned_ensembl_gene_id":"ENSG00000238745.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":138623479,"end":138623582,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000212558.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":10090205,"end":10090319,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000207163.1","gene_symbol":"RNU6-905P","gene_name":"RNA, U6 small nuclear 905, pseudogene [Source:HGNC Symbol;Acc:HGNC:47868]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479967","summary":null,"start":14530982,"end":14531088,"strand":-1,"description":"RNA, U6 small nuclear 905, pseudogene [Source:HGNC Symbol;Acc:HGNC:47868]"}, {"versioned_ensembl_gene_id":"ENSG00000222255.1","gene_symbol":"RNU6-101P","gene_name":"RNA, U6 small nuclear 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:47064]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479611","summary":null,"start":101765406,"end":101765509,"strand":-1,"description":"RNA, U6 small nuclear 101, pseudogene [Source:HGNC Symbol;Acc:HGNC:47064]"}, {"versioned_ensembl_gene_id":"ENSG00000222558.1","gene_symbol":"RNU6-1064P","gene_name":"RNA, U6 small nuclear 1064, pseudogene [Source:HGNC Symbol;Acc:HGNC:48027]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481515","summary":null,"start":107797744,"end":107797847,"strand":-1,"description":"RNA, U6 small nuclear 1064, pseudogene [Source:HGNC Symbol;Acc:HGNC:48027]"}, {"versioned_ensembl_gene_id":"ENSG00000274623.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54940611,"end":54940717,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000223256.1","gene_symbol":"RNU6-785P","gene_name":"RNA, U6 small nuclear 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:47748]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479913","summary":null,"start":138259595,"end":138259698,"strand":1,"description":"RNA, U6 small nuclear 785, pseudogene [Source:HGNC Symbol;Acc:HGNC:47748]"}, {"versioned_ensembl_gene_id":"ENSG00000206790.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100257688,"end":100257790,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200087.1","gene_symbol":"SNORA73B","gene_name":"small nucleolar RNA, H/ACA box 73B [Source:HGNC Symbol;Acc:HGNC:10116]","synonyms":"U17B,RNU17B,RNU105A,E1c","biotype":"snoRNA","ncbi_id":"26768","summary":null,"start":28508559,"end":28508762,"strand":1,"description":"small nucleolar RNA, H/ACA box 73B [Source:HGNC Symbol;Acc:HGNC:10116]"}, {"versioned_ensembl_gene_id":"ENSG00000274862.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43277978,"end":43278168,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000207322.1","gene_symbol":"RNU1-89P","gene_name":"RNA, U1 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:48431]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480412","summary":null,"start":135995929,"end":135996092,"strand":-1,"description":"RNA, U1 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:48431]"}, {"versioned_ensembl_gene_id":"ENSG00000252393.1","gene_symbol":"RNU6-1004P","gene_name":"RNA, U6 small nuclear 1004, pseudogene [Source:HGNC Symbol;Acc:HGNC:47967]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480009","summary":null,"start":121604902,"end":121605012,"strand":1,"description":"RNA, U6 small nuclear 1004, pseudogene [Source:HGNC Symbol;Acc:HGNC:47967]"}, {"versioned_ensembl_gene_id":"ENSG00000202459.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":102695388,"end":102695495,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199442.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":247997000,"end":247997096,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283334.1","gene_symbol":"hsa-mir-4536-1","gene_name":"hsa-mir-4536-1 [Source:miRBase;Acc:MI0016906]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":55451495,"end":55451582,"strand":-1,"description":"hsa-mir-4536-1 [Source:miRBase;Acc:MI0016906]"}, {"versioned_ensembl_gene_id":"ENSG00000283775.1","gene_symbol":"MIR4329","gene_name":"microRNA 4329 [Source:HGNC Symbol;Acc:HGNC:38290]","synonyms":"hsa-mir-4329","biotype":"miRNA","ncbi_id":"100423009","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112780718,"end":112780788,"strand":-1,"description":"microRNA 4329 [Source:HGNC Symbol;Acc:HGNC:38290]"}, {"versioned_ensembl_gene_id":"ENSG00000284310.1","gene_symbol":"MIR939","gene_name":"microRNA 939 [Source:HGNC Symbol;Acc:HGNC:33682]","synonyms":"MIRN939,hsa-mir-939","biotype":"miRNA","ncbi_id":"100126351","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144394149,"end":144394230,"strand":-1,"description":"microRNA 939 [Source:HGNC Symbol;Acc:HGNC:33682]"}, {"versioned_ensembl_gene_id":"ENSG00000200091.1","gene_symbol":"RN7SKP163","gene_name":"RNA, 7SK small nuclear pseudogene 163 [Source:HGNC Symbol;Acc:HGNC:45887]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479168","summary":null,"start":75654970,"end":75655299,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 163 [Source:HGNC Symbol;Acc:HGNC:45887]"}, {"versioned_ensembl_gene_id":"ENSG00000200340.1","gene_symbol":"RNU1-105P","gene_name":"RNA, U1 small nuclear 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:48447]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480185","summary":null,"start":47823390,"end":47823550,"strand":1,"description":"RNA, U1 small nuclear 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:48447]"}, {"versioned_ensembl_gene_id":"ENSG00000206595.1","gene_symbol":"RNU6-877P","gene_name":"RNA, U6 small nuclear 877, pseudogene [Source:HGNC Symbol;Acc:HGNC:47840]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480617","summary":null,"start":51382308,"end":51382414,"strand":1,"description":"RNA, U6 small nuclear 877, pseudogene [Source:HGNC Symbol;Acc:HGNC:47840]"}, {"versioned_ensembl_gene_id":"ENSG00000266160.2","gene_symbol":"RN7SL612P","gene_name":"RNA, 7SL, cytoplasmic 612, pseudogene [Source:HGNC Symbol;Acc:HGNC:46628]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479445","summary":null,"start":156985755,"end":156986049,"strand":-1,"description":"RNA, 7SL, cytoplasmic 612, pseudogene [Source:HGNC Symbol;Acc:HGNC:46628]"}, {"versioned_ensembl_gene_id":"ENSG00000202157.1","gene_symbol":"RNU4-11P","gene_name":"RNA, U4 small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46947]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481175","summary":null,"start":83803554,"end":83803685,"strand":1,"description":"RNA, U4 small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46947]"}, {"versioned_ensembl_gene_id":"ENSG00000283673.1","gene_symbol":"MIR4531","gene_name":"microRNA 4531 [Source:HGNC Symbol;Acc:HGNC:41872]","synonyms":"hsa-mir-4531","biotype":"miRNA","ncbi_id":"100616355","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44653686,"end":44653732,"strand":-1,"description":"microRNA 4531 [Source:HGNC Symbol;Acc:HGNC:41872]"}, {"versioned_ensembl_gene_id":"ENSG00000273739.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":122136,"end":122225,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000284162.1","gene_symbol":"MIR4523","gene_name":"microRNA 4523 [Source:HGNC Symbol;Acc:HGNC:41583]","synonyms":"hsa-mir-4523","biotype":"miRNA","ncbi_id":"100616122","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29390662,"end":29390730,"strand":1,"description":"microRNA 4523 [Source:HGNC Symbol;Acc:HGNC:41583]"}, {"versioned_ensembl_gene_id":"ENSG00000284112.1","gene_symbol":"MIR195","gene_name":"microRNA 195 [Source:HGNC Symbol;Acc:HGNC:31566]","synonyms":"MIRN195,hsa-mir-195","biotype":"miRNA","ncbi_id":"406971","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7017615,"end":7017701,"strand":-1,"description":"microRNA 195 [Source:HGNC Symbol;Acc:HGNC:31566]"}, {"versioned_ensembl_gene_id":"ENSG00000200527.1","gene_symbol":"RNA5SP457","gene_name":"RNA, 5S ribosomal pseudogene 457 [Source:HGNC Symbol;Acc:HGNC:43357]","synonyms":"RN5S457","biotype":"rRNA","ncbi_id":"100873702","summary":null,"start":49946266,"end":49946389,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 457 [Source:HGNC Symbol;Acc:HGNC:43357]"}, {"versioned_ensembl_gene_id":"ENSG00000265776.1","gene_symbol":"MIR3670-3","gene_name":"microRNA 3670-3 [Source:HGNC Symbol;Acc:HGNC:50829]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504726","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18405698,"end":18405762,"strand":-1,"description":"microRNA 3670-3 [Source:HGNC Symbol;Acc:HGNC:50829]"}, {"versioned_ensembl_gene_id":"ENSG00000221520.1","gene_symbol":"MIR1285-1","gene_name":"microRNA 1285-1 [Source:HGNC Symbol;Acc:HGNC:35277]","synonyms":"MIRN1285-1,hsa-mir-1285-1","biotype":"miRNA","ncbi_id":"100302218","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":92204015,"end":92204098,"strand":-1,"description":"microRNA 1285-1 [Source:HGNC Symbol;Acc:HGNC:35277]"}, {"versioned_ensembl_gene_id":"ENSG00000265745.2","gene_symbol":"RN7SL375P","gene_name":"RNA, 7SL, cytoplasmic 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:46391]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479359","summary":null,"start":60034465,"end":60034762,"strand":-1,"description":"RNA, 7SL, cytoplasmic 375, pseudogene [Source:HGNC Symbol;Acc:HGNC:46391]"}, {"versioned_ensembl_gene_id":"ENSG00000252655.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":89650793,"end":89650903,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252644.1","gene_symbol":"RNU7-30P","gene_name":"RNA, U7 small nuclear 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:34126]","synonyms":"U7.30","biotype":"snRNA","ncbi_id":"100147817","summary":null,"start":91091077,"end":91091138,"strand":1,"description":"RNA, U7 small nuclear 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:34126]"}, {"versioned_ensembl_gene_id":"ENSG00000276352.2","gene_symbol":"MIR668","gene_name":"microRNA 668 [Source:HGNC Symbol;Acc:HGNC:33135]","synonyms":"MIRN668,hsa-mir-668","biotype":"miRNA","ncbi_id":"768214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101055258,"end":101055323,"strand":1,"description":"microRNA 668 [Source:HGNC Symbol;Acc:HGNC:33135]"}, {"versioned_ensembl_gene_id":"ENSG00000262776.1","gene_symbol":"RN7SKP65","gene_name":"RNA, 7SK small nuclear pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:45789]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479124","summary":null,"start":57977965,"end":57978277,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:45789]"}, {"versioned_ensembl_gene_id":"ENSG00000284008.1","gene_symbol":"MIR6511B1","gene_name":"microRNA 6511b-1 [Source:HGNC Symbol;Acc:HGNC:50228]","synonyms":"hsa-mir-6511b-1","biotype":"miRNA","ncbi_id":"102465429","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2106669,"end":2106753,"strand":-1,"description":"microRNA 6511b-1 [Source:HGNC Symbol;Acc:HGNC:50228]"}, {"versioned_ensembl_gene_id":"ENSG00000265322.1","gene_symbol":"MIR3118-2","gene_name":"microRNA 3118-2 [Source:HGNC Symbol;Acc:HGNC:38324]","synonyms":"hsa-mir-3118-2","biotype":"miRNA","ncbi_id":"100422949","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20832795,"end":20832869,"strand":1,"description":"microRNA 3118-2 [Source:HGNC Symbol;Acc:HGNC:38324]"}, {"versioned_ensembl_gene_id":"ENSG00000212609.1","gene_symbol":"RNU1-139P","gene_name":"RNA, U1 small nuclear 139, pseudogene [Source:HGNC Symbol;Acc:HGNC:48481]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480196","summary":null,"start":19345148,"end":19345312,"strand":1,"description":"RNA, U1 small nuclear 139, pseudogene [Source:HGNC Symbol;Acc:HGNC:48481]"}, {"versioned_ensembl_gene_id":"ENSG00000206866.1","gene_symbol":"RNU6-187P","gene_name":"RNA, U6 small nuclear 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:47150]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481880","summary":null,"start":176929985,"end":176930090,"strand":-1,"description":"RNA, U6 small nuclear 187, pseudogene [Source:HGNC Symbol;Acc:HGNC:47150]"}, {"versioned_ensembl_gene_id":"ENSG00000278267.1","gene_symbol":"MIR6859-1","gene_name":"microRNA 6859-1 [Source:HGNC Symbol;Acc:HGNC:50039]","synonyms":"hsa-mir-6859-1","biotype":"miRNA","ncbi_id":"102466751","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17369,"end":17436,"strand":-1,"description":"microRNA 6859-1 [Source:HGNC Symbol;Acc:HGNC:50039]"}, {"versioned_ensembl_gene_id":"ENSG00000276089.1","gene_symbol":"DLEU1_1","gene_name":"Deleted in lymphocytic leukemia 1 conserved region 1 [Source:RFAM;Acc:RF02103]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50082295,"end":50082484,"strand":1,"description":"Deleted in lymphocytic leukemia 1 conserved region 1 [Source:RFAM;Acc:RF02103]"}, {"versioned_ensembl_gene_id":"ENSG00000281159.1","gene_symbol":"SCARNA15","gene_name":"Small Cajal body specific RNA 15 [Source:RFAM;Acc:RF00426]","synonyms":"ACA45,ACA45","biotype":"scaRNA","ncbi_id":"677778","summary":null,"start":130929762,"end":130929883,"strand":-1,"description":"Small Cajal body specific RNA 15 [Source:RFAM;Acc:RF00426]"}, {"versioned_ensembl_gene_id":"ENSG00000277607.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000275531.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153700659,"end":153700956,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000206762.1","gene_symbol":"RNU6-418P","gene_name":"RNA, U6 small nuclear 418, pseudogene [Source:HGNC Symbol;Acc:HGNC:47381]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481310","summary":null,"start":205595041,"end":205595147,"strand":1,"description":"RNA, U6 small nuclear 418, pseudogene [Source:HGNC Symbol;Acc:HGNC:47381]"}, {"versioned_ensembl_gene_id":"ENSG00000241756.3","gene_symbol":"RN7SL83P","gene_name":"RNA, 7SL, cytoplasmic 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:46099]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479254","summary":null,"start":38531042,"end":38531338,"strand":-1,"description":"RNA, 7SL, cytoplasmic 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:46099]"}, {"versioned_ensembl_gene_id":"ENSG00000199204.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34001698,"end":34001799,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222460.1","gene_symbol":"RN7SKP271","gene_name":"RNA, 7SK small nuclear pseudogene 271 [Source:HGNC Symbol;Acc:HGNC:45995]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480916","summary":null,"start":35643143,"end":35643462,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 271 [Source:HGNC Symbol;Acc:HGNC:45995]"}, {"versioned_ensembl_gene_id":"ENSG00000239099.1","gene_symbol":"RNU7-23P","gene_name":"RNA, U7 small nuclear 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:34119]","synonyms":"U7.23","biotype":"snRNA","ncbi_id":"100147771","summary":null,"start":66919762,"end":66919823,"strand":1,"description":"RNA, U7 small nuclear 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:34119]"}, {"versioned_ensembl_gene_id":"ENSG00000278752.1","gene_symbol":"AL355301.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":98076361,"end":98076421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278397.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30047700,"end":30047775,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000251880.1","gene_symbol":"RNU7-75P","gene_name":"RNA, U7 small nuclear 75 pseudogene [Source:HGNC Symbol;Acc:HGNC:34171]","synonyms":"U7.75","biotype":"snRNA","ncbi_id":"100151672","summary":null,"start":37327135,"end":37327196,"strand":1,"description":"RNA, U7 small nuclear 75 pseudogene [Source:HGNC Symbol;Acc:HGNC:34171]"}, {"versioned_ensembl_gene_id":"ENSG00000221381.1","gene_symbol":"SNORD88B","gene_name":"small nucleolar RNA, C/D box 88B [Source:HGNC Symbol;Acc:HGNC:32748]","synonyms":"HBII-180B","biotype":"snoRNA","ncbi_id":"692203","summary":null,"start":50799032,"end":50799122,"strand":-1,"description":"small nucleolar RNA, C/D box 88B [Source:HGNC Symbol;Acc:HGNC:32748]"}, {"versioned_ensembl_gene_id":"ENSG00000266507.1","gene_symbol":"MIR4479","gene_name":"microRNA 4479 [Source:HGNC Symbol;Acc:HGNC:41767]","synonyms":"hsa-mir-4479","biotype":"miRNA","ncbi_id":"100616480","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136886733,"end":136886803,"strand":1,"description":"microRNA 4479 [Source:HGNC Symbol;Acc:HGNC:41767]"}, {"versioned_ensembl_gene_id":"ENSG00000206996.1","gene_symbol":"RNU6-842P","gene_name":"RNA, U6 small nuclear 842, pseudogene [Source:HGNC Symbol;Acc:HGNC:47805]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481447","summary":null,"start":13044350,"end":13044456,"strand":1,"description":"RNA, U6 small nuclear 842, pseudogene [Source:HGNC Symbol;Acc:HGNC:47805]"}, {"versioned_ensembl_gene_id":"ENSG00000264810.1","gene_symbol":"MIR4441","gene_name":"microRNA 4441 [Source:HGNC Symbol;Acc:HGNC:41728]","synonyms":"hsa-mir-4441","biotype":"miRNA","ncbi_id":"100616493","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239085827,"end":239085926,"strand":-1,"description":"microRNA 4441 [Source:HGNC Symbol;Acc:HGNC:41728]"}, {"versioned_ensembl_gene_id":"ENSG00000284159.1","gene_symbol":"MIR3940","gene_name":"microRNA 3940 [Source:HGNC Symbol;Acc:HGNC:38893]","synonyms":"hsa-mir-3940","biotype":"miRNA","ncbi_id":"100500888","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6416410,"end":6416511,"strand":-1,"description":"microRNA 3940 [Source:HGNC Symbol;Acc:HGNC:38893]"}, {"versioned_ensembl_gene_id":"ENSG00000206635.1","gene_symbol":"RNU6-1062P","gene_name":"RNA, U6 small nuclear 1062, pseudogene [Source:HGNC Symbol;Acc:HGNC:48025]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480634","summary":null,"start":151629324,"end":151629430,"strand":1,"description":"RNA, U6 small nuclear 1062, pseudogene [Source:HGNC Symbol;Acc:HGNC:48025]"}, {"versioned_ensembl_gene_id":"ENSG00000244294.3","gene_symbol":"RN7SL740P","gene_name":"RNA, 7SL, cytoplasmic 740, pseudogene [Source:HGNC Symbol;Acc:HGNC:46756]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479491","summary":null,"start":33918995,"end":33919338,"strand":-1,"description":"RNA, 7SL, cytoplasmic 740, pseudogene [Source:HGNC Symbol;Acc:HGNC:46756]"}, {"versioned_ensembl_gene_id":"ENSG00000201500.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA 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{"versioned_ensembl_gene_id":"ENSG00000238808.1","gene_symbol":"RNU7-102P","gene_name":"RNA, U7 small nuclear 102 pseudogene [Source:HGNC Symbol;Acc:HGNC:45636]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479064","summary":null,"start":69110513,"end":69110574,"strand":-1,"description":"RNA, U7 small nuclear 102 pseudogene [Source:HGNC Symbol;Acc:HGNC:45636]"}, {"versioned_ensembl_gene_id":"ENSG00000212168.1","gene_symbol":"SNORD78","gene_name":"Small nucleolar RNA SNORD78 [Source:RFAM;Acc:RF00592]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692198","summary":null,"start":57544535,"end":57544599,"strand":1,"description":"Small nucleolar RNA SNORD78 [Source:RFAM;Acc:RF00592]"}, {"versioned_ensembl_gene_id":"ENSG00000201271.1","gene_symbol":"RNU1-112P","gene_name":"RNA, U1 small nuclear 112, pseudogene [Source:HGNC Symbol;Acc:HGNC:48454]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480187","summary":null,"start":72740706,"end":72740869,"strand":-1,"description":"RNA, U1 small 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{"versioned_ensembl_gene_id":"ENSG00000265028.1","gene_symbol":"MIR4792","gene_name":"microRNA 4792 [Source:HGNC Symbol;Acc:HGNC:41577]","synonyms":"miR-4792,hsa-mir-4792","biotype":"miRNA","ncbi_id":"100616448","summary":"This record was withdrawn by miRBase.","start":24521362,"end":24521435,"strand":-1,"description":"microRNA 4792 [Source:HGNC Symbol;Acc:HGNC:41577]"}, {"versioned_ensembl_gene_id":"ENSG00000252467.1","gene_symbol":"RNU6-347P","gene_name":"RNA, U6 small nuclear 347, pseudogene [Source:HGNC Symbol;Acc:HGNC:47310]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479720","summary":null,"start":51902291,"end":51902395,"strand":1,"description":"RNA, U6 small nuclear 347, pseudogene [Source:HGNC Symbol;Acc:HGNC:47310]"}, {"versioned_ensembl_gene_id":"ENSG00000252995.1","gene_symbol":"RNU6-667P","gene_name":"RNA, U6 small nuclear 667, pseudogene [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2274620,"end":2274691,"strand":1,"description":"microRNA 4717 [Source:HGNC Symbol;Acc:HGNC:41571]"}, {"versioned_ensembl_gene_id":"ENSG00000278851.1","gene_symbol":"MIR6879","gene_name":"microRNA 6879 [Source:HGNC Symbol;Acc:HGNC:49957]","synonyms":"hsa-mir-6879","biotype":"miRNA","ncbi_id":"102466756","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65018505,"end":65018570,"strand":1,"description":"microRNA 6879 [Source:HGNC Symbol;Acc:HGNC:49957]"}, {"versioned_ensembl_gene_id":"ENSG00000238649.1","gene_symbol":"SNORD42A","gene_name":"small nucleolar RNA, C/D box 42A [Source:HGNC Symbol;Acc:HGNC:10180]","synonyms":"U42,RNU42A","biotype":"snoRNA","ncbi_id":"26809","summary":null,"start":28723429,"end":28723492,"strand":1,"description":"small nucleolar RNA, C/D box 42A [Source:HGNC Symbol;Acc:HGNC:10180]"}, {"versioned_ensembl_gene_id":"ENSG00000206759.1","gene_symbol":"RNU6-787P","gene_name":"RNA, U6 small nuclear 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:47750]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479914","summary":null,"start":66293114,"end":66293220,"strand":-1,"description":"RNA, U6 small nuclear 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:47750]"}, {"versioned_ensembl_gene_id":"ENSG00000239143.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85332895,"end":85332996,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200591.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32639951,"end":32640052,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222726.1","gene_symbol":"RNU2-7P","gene_name":"RNA, U2 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42505]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873824","summary":null,"start":20612161,"end":20612338,"strand":1,"description":"RNA, U2 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42505]"}, {"versioned_ensembl_gene_id":"ENSG00000284499.1","gene_symbol":"MIR363","gene_name":"microRNA 363 [Source:HGNC Symbol;Acc:HGNC:32023]","synonyms":"MIRN363,MIR-363,hsa-mir-363","biotype":"miRNA","ncbi_id":"574031","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134169378,"end":134169452,"strand":-1,"description":"microRNA 363 [Source:HGNC Symbol;Acc:HGNC:32023]"}, {"versioned_ensembl_gene_id":"ENSG00000223145.1","gene_symbol":"RN7SKP112","gene_name":"RNA, 7SK small nuclear pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:45836]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479145","summary":null,"start":7141227,"end":7141544,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:45836]"}, {"versioned_ensembl_gene_id":"ENSG00000238363.1","gene_symbol":"SNORA13","gene_name":"small nucleolar RNA, H/ACA box 13 [Source:HGNC Symbol;Acc:HGNC:32601]","synonyms":"ACA13","biotype":"snoRNA","ncbi_id":"654322","summary":null,"start":112161485,"end":112161617,"strand":1,"description":"small nucleolar RNA, H/ACA box 13 [Source:HGNC Symbol;Acc:HGNC:32601]"}, {"versioned_ensembl_gene_id":"ENSG00000263892.3","gene_symbol":"MIR4667","gene_name":"microRNA 4667 [Source:HGNC Symbol;Acc:HGNC:41723]","synonyms":"hsa-mir-4667","biotype":"miRNA","ncbi_id":"100616214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35608094,"end":35608159,"strand":1,"description":"microRNA 4667 [Source:HGNC Symbol;Acc:HGNC:41723]"}, {"versioned_ensembl_gene_id":"ENSG00000265828.1","gene_symbol":"MIR3939","gene_name":"microRNA 3939 [Source:HGNC Symbol;Acc:HGNC:38931]","synonyms":"hsa-mir-3939","biotype":"miRNA","ncbi_id":"100500857","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":166997807,"end":166997912,"strand":-1,"description":"microRNA 3939 [Source:HGNC Symbol;Acc:HGNC:38931]"}, {"versioned_ensembl_gene_id":"ENSG00000206958.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":88382772,"end":88382907,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000274606.1","gene_symbol":"ST7-OT4_4","gene_name":"ST7 overlapping transcript 4 conserved region 4 [Source:RFAM;Acc:RF02190]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116959593,"end":116959805,"strand":1,"description":"ST7 overlapping transcript 4 conserved region 4 [Source:RFAM;Acc:RF02190]"}, {"versioned_ensembl_gene_id":"ENSG00000262656.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":141733992,"end":141734156,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000266396.1","gene_symbol":"MIR4273","gene_name":"microRNA 4273 [Source:HGNC Symbol;Acc:HGNC:38339]","synonyms":"hsa-mir-4273","biotype":"miRNA","ncbi_id":"100422955","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75738280,"end":75738363,"strand":1,"description":"microRNA 4273 [Source:HGNC Symbol;Acc:HGNC:38339]"}, {"versioned_ensembl_gene_id":"ENSG00000276256.1","gene_symbol":"AC011043.1","gene_name":"Homo sapiens uncharacterized LOC389831 (LOC389831), transcript variant 3, mRNA. [Source:RefSeq mRNA;Acc:NM_001347681]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42939,"end":49164,"strand":-1,"description":"Homo sapiens uncharacterized LOC389831 (LOC389831), transcript variant 3, mRNA. [Source:RefSeq mRNA;Acc:NM_001347681]"}, {"versioned_ensembl_gene_id":"ENSG00000276082.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000275863.1","gene_symbol":"MIR7975","gene_name":"microRNA 7975 [Source:HGNC Symbol;Acc:HGNC:49967]","synonyms":"hsa-mir-7975","biotype":"miRNA","ncbi_id":"102466872","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55123225,"end":55123292,"strand":-1,"description":"microRNA 7975 [Source:HGNC Symbol;Acc:HGNC:49967]"}, {"versioned_ensembl_gene_id":"ENSG00000278089.1","gene_symbol":"SNORD115-7","gene_name":"small nucleolar RNA, C/D box 115-7 [Source:HGNC Symbol;Acc:HGNC:33026]","synonyms":"HBII-52-7","biotype":"snoRNA","ncbi_id":"100033444","summary":null,"start":25182385,"end":25182466,"strand":1,"description":"small nucleolar RNA, C/D box 115-7 [Source:HGNC Symbol;Acc:HGNC:33026]"}, {"versioned_ensembl_gene_id":"ENSG00000200294.1","gene_symbol":"SNORA36","gene_name":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":72180858,"end":72180989,"strand":1,"description":"Small nucleolar RNA SNORA36 family [Source:RFAM;Acc:RF00340]"}, {"versioned_ensembl_gene_id":"ENSG00000199069.3","gene_symbol":"MIR323A","gene_name":"microRNA 323a [Source:HGNC Symbol;Acc:HGNC:31766]","synonyms":"MIRN323,MIR323,hsa-mir-323","biotype":"miRNA","ncbi_id":"442897","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101025732,"end":101025817,"strand":1,"description":"microRNA 323a [Source:HGNC Symbol;Acc:HGNC:31766]"}, {"versioned_ensembl_gene_id":"ENSG00000265905.2","gene_symbol":"RN7SL96P","gene_name":"RNA, 7SL, cytoplasmic 96, pseudogene [Source:HGNC Symbol;Acc:HGNC:46112]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480486","summary":null,"start":38936876,"end":38937158,"strand":-1,"description":"RNA, 7SL, cytoplasmic 96, pseudogene [Source:HGNC Symbol;Acc:HGNC:46112]"}, {"versioned_ensembl_gene_id":"ENSG00000277187.1","gene_symbol":"RN7SL268P","gene_name":"RNA, 7SL, cytoplasmic 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:46284]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479319","summary":null,"start":23879493,"end":23879790,"strand":-1,"description":"RNA, 7SL, cytoplasmic 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:46284]"}, {"versioned_ensembl_gene_id":"ENSG00000212314.2","gene_symbol":"RNU6-1307P","gene_name":"RNA, U6 small nuclear 1307, pseudogene [Source:HGNC Symbol;Acc:HGNC:48270]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481593","summary":null,"start":54263951,"end":54264053,"strand":-1,"description":"RNA, U6 small nuclear 1307, pseudogene [Source:HGNC Symbol;Acc:HGNC:48270]"}, {"versioned_ensembl_gene_id":"ENSG00000212489.1","gene_symbol":"RNU6-1109P","gene_name":"RNA, U6 small nuclear 1109, pseudogene [Source:HGNC Symbol;Acc:HGNC:48072]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480054","summary":null,"start":190165417,"end":190165523,"strand":-1,"description":"RNA, U6 small nuclear 1109, pseudogene [Source:HGNC Symbol;Acc:HGNC:48072]"}, {"versioned_ensembl_gene_id":"ENSG00000206944.1","gene_symbol":"RNU6-708P","gene_name":"RNA, U6 small nuclear 708, pseudogene [Source:HGNC Symbol;Acc:HGNC:47671]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480602","summary":null,"start":48169784,"end":48169890,"strand":-1,"description":"RNA, U6 small nuclear 708, pseudogene [Source:HGNC Symbol;Acc:HGNC:47671]"}, {"versioned_ensembl_gene_id":"ENSG00000207820.1","gene_symbol":"MIR545","gene_name":"microRNA 545 [Source:HGNC Symbol;Acc:HGNC:32531]","synonyms":"MIRN545,hsa-mir-545","biotype":"miRNA","ncbi_id":"664614","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74287104,"end":74287209,"strand":-1,"description":"microRNA 545 [Source:HGNC Symbol;Acc:HGNC:32531]"}, {"versioned_ensembl_gene_id":"ENSG00000207323.1","gene_symbol":"RNU6-901P","gene_name":"RNA, U6 small nuclear 901, pseudogene [Source:HGNC Symbol;Acc:HGNC:47864]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479965","summary":null,"start":153471466,"end":153471571,"strand":-1,"description":"RNA, U6 small nuclear 901, pseudogene [Source:HGNC Symbol;Acc:HGNC:47864]"}, {"versioned_ensembl_gene_id":"ENSG00000206885.1","gene_symbol":"SNORA75","gene_name":"small nucleolar RNA, H/ACA box 75 [Source:HGNC Symbol;Acc:HGNC:32661]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":231455800,"end":231455936,"strand":-1,"description":"small nucleolar RNA, H/ACA box 75 [Source:HGNC Symbol;Acc:HGNC:32661]"}, {"versioned_ensembl_gene_id":"ENSG00000253020.2","gene_symbol":"RN7SKP40","gene_name":"RNA, 7SK small nuclear pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:45764]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479113","summary":null,"start":174631823,"end":174632064,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:45764]"}, {"versioned_ensembl_gene_id":"ENSG00000252542.1","gene_symbol":"SNORD36C","gene_name":"small nucleolar RNA, C/D box 36C [Source:HGNC Symbol;Acc:HGNC:10165]","synonyms":"U36c,RNU36C","biotype":"snoRNA","ncbi_id":"26813","summary":null,"start":133350847,"end":133350912,"strand":1,"description":"small nucleolar RNA, C/D box 36C [Source:HGNC Symbol;Acc:HGNC:10165]"}, {"versioned_ensembl_gene_id":"ENSG00000266761.1","gene_symbol":"MIR3194","gene_name":"microRNA 3194 [Source:HGNC Symbol;Acc:HGNC:38346]","synonyms":"hsa-mir-3194","biotype":"miRNA","ncbi_id":"100422889","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51452905,"end":51452977,"strand":-1,"description":"microRNA 3194 [Source:HGNC Symbol;Acc:HGNC:38346]"}, {"versioned_ensembl_gene_id":"ENSG00000212593.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":23441841,"end":23441921,"strand":1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000266431.1","gene_symbol":"MIR5580","gene_name":"microRNA 5580 [Source:HGNC Symbol;Acc:HGNC:43482]","synonyms":"hsa-mir-5580","biotype":"miRNA","ncbi_id":"100847076","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53948427,"end":53948484,"strand":-1,"description":"microRNA 5580 [Source:HGNC Symbol;Acc:HGNC:43482]"}, {"versioned_ensembl_gene_id":"ENSG00000274011.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":98115885,"end":98116135,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252237.1","gene_symbol":"RNU4-54P","gene_name":"RNA, U4 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:46990]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479583","summary":null,"start":28319335,"end":28319463,"strand":-1,"description":"RNA, U4 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:46990]"}, {"versioned_ensembl_gene_id":"ENSG00000221603.1","gene_symbol":"MIR1184-3","gene_name":"microRNA 1184-3 [Source:HGNC Symbol;Acc:HGNC:38389]","synonyms":"hsa-mir-1184-3","biotype":"miRNA","ncbi_id":"100422977","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155457517,"end":155457615,"strand":1,"description":"microRNA 1184-3 [Source:HGNC Symbol;Acc:HGNC:38389]"}, {"versioned_ensembl_gene_id":"ENSG00000216075.1","gene_symbol":"MIR890","gene_name":"microRNA 890 [Source:HGNC Symbol;Acc:HGNC:33644]","synonyms":"MIRN890,hsa-mir-890","biotype":"miRNA","ncbi_id":"100126303","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145994275,"end":145994351,"strand":-1,"description":"microRNA 890 [Source:HGNC Symbol;Acc:HGNC:33644]"}, {"versioned_ensembl_gene_id":"ENSG00000206754.1","gene_symbol":"SNORD101","gene_name":"small nucleolar RNA, C/D box 101 [Source:HGNC Symbol;Acc:HGNC:32764]","synonyms":"U101","biotype":"snoRNA","ncbi_id":"594837","summary":null,"start":132815307,"end":132815379,"strand":1,"description":"small nucleolar RNA, C/D box 101 [Source:HGNC Symbol;Acc:HGNC:32764]"}, {"versioned_ensembl_gene_id":"ENSG00000207870.1","gene_symbol":"MIR221","gene_name":"microRNA 221 [Source:HGNC Symbol;Acc:HGNC:31601]","synonyms":"MIRN221,hsa-mir-221","biotype":"miRNA","ncbi_id":"407006","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45746157,"end":45746266,"strand":-1,"description":"microRNA 221 [Source:HGNC Symbol;Acc:HGNC:31601]"}, {"versioned_ensembl_gene_id":"ENSG00000283857.1","gene_symbol":"MIR1247","gene_name":"microRNA 1247 [Source:HGNC Symbol;Acc:HGNC:35313]","synonyms":"MIRN1247,hsa-mir-1247","biotype":"miRNA","ncbi_id":"100302145","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101560287,"end":101560422,"strand":-1,"description":"microRNA 1247 [Source:HGNC Symbol;Acc:HGNC:35313]"}, {"versioned_ensembl_gene_id":"ENSG00000211563.4","gene_symbol":"MIR3065","gene_name":"microRNA 3065 [Source:HGNC Symbol;Acc:HGNC:38234]","synonyms":"hsa-mir-3065","biotype":"miRNA","ncbi_id":"100422915","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81125877,"end":81125955,"strand":1,"description":"microRNA 3065 [Source:HGNC Symbol;Acc:HGNC:38234]"}, {"versioned_ensembl_gene_id":"ENSG00000207952.1","gene_symbol":"MIR624","gene_name":"microRNA 624 [Source:HGNC Symbol;Acc:HGNC:32880]","synonyms":"MIRN624,hsa-mir-624","biotype":"miRNA","ncbi_id":"693209","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31014646,"end":31014742,"strand":-1,"description":"microRNA 624 [Source:HGNC Symbol;Acc:HGNC:32880]"}, {"versioned_ensembl_gene_id":"ENSG00000277269.1","gene_symbol":"MESTIT1_1","gene_name":"MEST intronic transcript 1, antisense RNA conserved region 1 [Source:RFAM;Acc:RF02148]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130487483,"end":130487622,"strand":1,"description":"MEST intronic transcript 1, antisense RNA conserved region 1 [Source:RFAM;Acc:RF02148]"}, {"versioned_ensembl_gene_id":"ENSG00000244034.3","gene_symbol":"RN7SL424P","gene_name":"RNA, 7SL, cytoplasmic 424, pseudogene [Source:HGNC Symbol;Acc:HGNC:46440]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480376","summary":null,"start":55063738,"end":55064026,"strand":1,"description":"RNA, 7SL, cytoplasmic 424, pseudogene [Source:HGNC Symbol;Acc:HGNC:46440]"}, {"versioned_ensembl_gene_id":"ENSG00000202429.1","gene_symbol":"RNU4-48P","gene_name":"RNA, U4 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:46984]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479580","summary":null,"start":127472234,"end":127472415,"strand":1,"description":"RNA, U4 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:46984]"}, {"versioned_ensembl_gene_id":"ENSG00000274617.1","gene_symbol":"RFPL3-AS1_1","gene_name":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32362972,"end":32363059,"strand":1,"description":"RFPL3 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02171]"}, {"versioned_ensembl_gene_id":"ENSG00000265872.1","gene_symbol":"MIR3689A","gene_name":"microRNA 3689a [Source:HGNC Symbol;Acc:HGNC:38904]","synonyms":"hsa-mir-3689a","biotype":"miRNA","ncbi_id":"100500846","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134849487,"end":134849564,"strand":-1,"description":"microRNA 3689a [Source:HGNC Symbol;Acc:HGNC:38904]"}, {"versioned_ensembl_gene_id":"ENSG00000208012.1","gene_symbol":"MIRLET7F2","gene_name":"microRNA let-7f-2 [Source:HGNC Symbol;Acc:HGNC:31484]","synonyms":"MIRNLET7F2,hsa-let-7f-2","biotype":"miRNA","ncbi_id":"406889","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53557192,"end":53557274,"strand":-1,"description":"microRNA let-7f-2 [Source:HGNC Symbol;Acc:HGNC:31484]"}, {"versioned_ensembl_gene_id":"ENSG00000199306.1","gene_symbol":"RNU6-858P","gene_name":"RNA, U6 small nuclear 858, pseudogene [Source:HGNC Symbol;Acc:HGNC:47821]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479945","summary":null,"start":197894507,"end":197894613,"strand":1,"description":"RNA, U6 small nuclear 858, pseudogene [Source:HGNC Symbol;Acc:HGNC:47821]"}, {"versioned_ensembl_gene_id":"ENSG00000200065.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32134738,"end":32134834,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276594.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30139580,"end":30139683,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000216001.3","gene_symbol":"MIR450B","gene_name":"microRNA 450b [Source:HGNC Symbol;Acc:HGNC:33642]","synonyms":"MIRN450B,hsa-mir-450b","biotype":"miRNA","ncbi_id":"100126302","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134540185,"end":134540262,"strand":-1,"description":"microRNA 450b [Source:HGNC Symbol;Acc:HGNC:33642]"}, {"versioned_ensembl_gene_id":"ENSG00000266128.2","gene_symbol":"RN7SL366P","gene_name":"RNA, 7SL, cytoplasmic 366, pseudogene [Source:HGNC Symbol;Acc:HGNC:46382]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481023","summary":null,"start":163840561,"end":163840852,"strand":1,"description":"RNA, 7SL, cytoplasmic 366, pseudogene [Source:HGNC Symbol;Acc:HGNC:46382]"}, {"versioned_ensembl_gene_id":"ENSG00000202021.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75325959,"end":75326060,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274770.1","gene_symbol":"MIR6128","gene_name":"microRNA 6128 [Source:HGNC Symbol;Acc:HGNC:50109]","synonyms":"hsa-mir-6128","biotype":"miRNA","ncbi_id":"102465135","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56743873,"end":56743981,"strand":1,"description":"microRNA 6128 [Source:HGNC Symbol;Acc:HGNC:50109]"}, {"versioned_ensembl_gene_id":"ENSG00000202237.1","gene_symbol":"RNU6-53P","gene_name":"RNA, U6 small nuclear 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:42543]","synonyms":"RNU6-53","biotype":"snRNA","ncbi_id":"100873762","summary":null,"start":28703702,"end":28703807,"strand":-1,"description":"RNA, U6 small nuclear 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:42543]"}, {"versioned_ensembl_gene_id":"ENSG00000212434.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":69692956,"end":69693155,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000201153.1","gene_symbol":"RNU6-371P","gene_name":"RNA, U6 small nuclear 371, pseudogene [Source:HGNC Symbol;Acc:HGNC:47334]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479731","summary":null,"start":62298149,"end":62298256,"strand":-1,"description":"RNA, U6 small nuclear 371, pseudogene [Source:HGNC Symbol;Acc:HGNC:47334]"}, {"versioned_ensembl_gene_id":"ENSG00000273544.1","gene_symbol":"SNORA44","gene_name":"small nucleolar RNA, H/ACA box 44 [Source:HGNC Symbol;Acc:HGNC:32637]","synonyms":"ACA44","biotype":"snoRNA","ncbi_id":"677825","summary":null,"start":28580381,"end":28580512,"strand":-1,"description":"small nucleolar RNA, H/ACA box 44 [Source:HGNC Symbol;Acc:HGNC:32637]"}, {"versioned_ensembl_gene_id":"ENSG00000199381.1","gene_symbol":"RNU6-79P","gene_name":"RNA, U6 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:42569]","synonyms":"RNU6-79","biotype":"snRNA","ncbi_id":"100873779","summary":null,"start":72881108,"end":72881214,"strand":-1,"description":"RNA, U6 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:42569]"}, {"versioned_ensembl_gene_id":"ENSG00000265926.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29582205,"end":29582288,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000207704.2","gene_symbol":"MIR548AA1","gene_name":"microRNA 548aa-1 [Source:HGNC Symbol;Acc:HGNC:38944]","synonyms":"hsa-mir-548aa-1","biotype":"miRNA","ncbi_id":"100500863","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123348034,"end":123348130,"strand":1,"description":"microRNA 548aa-1 [Source:HGNC Symbol;Acc:HGNC:38944]"}, {"versioned_ensembl_gene_id":"ENSG00000284054.1","gene_symbol":"MIR7112","gene_name":"microRNA 7112 [Source:HGNC Symbol;Acc:HGNC:50149]","synonyms":"MIR7112-2,MIR7112-1,hsa-mir-7112-2,hsa-mir-7112-1","biotype":"miRNA","ncbi_id":"102465906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144262673,"end":144262737,"strand":-1,"description":"microRNA 7112 [Source:HGNC Symbol;Acc:HGNC:50149]"}, {"versioned_ensembl_gene_id":"ENSG00000221754.1","gene_symbol":"MIR1260A","gene_name":"microRNA 1260a [Source:HGNC Symbol;Acc:HGNC:35325]","synonyms":"MIRN1260,MIR1260,hsa-mir-1260","biotype":"miRNA","ncbi_id":"100302236","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77266218,"end":77266290,"strand":1,"description":"microRNA 1260a [Source:HGNC Symbol;Acc:HGNC:35325]"}, {"versioned_ensembl_gene_id":"ENSG00000199020.3","gene_symbol":"MIR381","gene_name":"microRNA 381 [Source:HGNC Symbol;Acc:HGNC:31874]","synonyms":"MIRN381,hsa-mir-381","biotype":"miRNA","ncbi_id":"494330","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101045920,"end":101045994,"strand":1,"description":"microRNA 381 [Source:HGNC Symbol;Acc:HGNC:31874]"}, {"versioned_ensembl_gene_id":"ENSG00000201274.1","gene_symbol":"RNA5SP192","gene_name":"RNA, 5S ribosomal pseudogene 192 [Source:HGNC Symbol;Acc:HGNC:43092]","synonyms":"RN5S192","biotype":"rRNA","ncbi_id":"100873454","summary":null,"start":132848577,"end":132848696,"strand":1,"description":"RNA, 5S ribosomal pseudogene 192 [Source:HGNC Symbol;Acc:HGNC:43092]"}, {"versioned_ensembl_gene_id":"ENSG00000240750.3","gene_symbol":"RN7SL559P","gene_name":"RNA, 7SL, cytoplasmic 559, pseudogene [Source:HGNC Symbol;Acc:HGNC:46575]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481849","summary":null,"start":28031884,"end":28032180,"strand":-1,"description":"RNA, 7SL, cytoplasmic 559, pseudogene [Source:HGNC Symbol;Acc:HGNC:46575]"}, {"versioned_ensembl_gene_id":"ENSG00000276426.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":91844022,"end":91844116,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000283788.1","gene_symbol":"MIR936","gene_name":"microRNA 936 [Source:HGNC Symbol;Acc:HGNC:33679]","synonyms":"hsa-mir-936,MIRN936","biotype":"miRNA","ncbi_id":"100126326","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104048089,"end":104048186,"strand":-1,"description":"microRNA 936 [Source:HGNC Symbol;Acc:HGNC:33679]"}, {"versioned_ensembl_gene_id":"ENSG00000278604.1","gene_symbol":"RN7SL429P","gene_name":"RNA, 7SL, cytoplasmic 429, pseudogene [Source:HGNC Symbol;Acc:HGNC:46445]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479380","summary":null,"start":74072454,"end":74072676,"strand":-1,"description":"RNA, 7SL, cytoplasmic 429, pseudogene [Source:HGNC Symbol;Acc:HGNC:46445]"}, {"versioned_ensembl_gene_id":"ENSG00000222185.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100998467,"end":100998541,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000252138.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":7726841,"end":7726951,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000278324.1","gene_symbol":"PVT1_3","gene_name":"Pvt1 oncogene conserved region 3 [Source:RFAM;Acc:RF02166]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127890626,"end":127890720,"strand":1,"description":"Pvt1 oncogene conserved region 3 [Source:RFAM;Acc:RF02166]"}, {"versioned_ensembl_gene_id":"ENSG00000200394.1","gene_symbol":"SNORA38B","gene_name":"small nucleolar RNA, H/ACA box 38B [Source:HGNC Symbol;Acc:HGNC:33617]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124536","summary":null,"start":67740669,"end":67740799,"strand":1,"description":"small nucleolar RNA, H/ACA box 38B [Source:HGNC Symbol;Acc:HGNC:33617]"}, {"versioned_ensembl_gene_id":"ENSG00000265867.1","gene_symbol":"MIR4516","gene_name":"microRNA 4516 [Source:HGNC Symbol;Acc:HGNC:41617]","synonyms":"hsa-mir-4516","biotype":"miRNA","ncbi_id":"100616258","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2133119,"end":2133204,"strand":1,"description":"microRNA 4516 [Source:HGNC Symbol;Acc:HGNC:41617]"}, {"versioned_ensembl_gene_id":"ENSG00000277546.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":38556066,"end":38556187,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000280792.1","gene_symbol":"AC093802.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239734956,"end":239735538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252726.1","gene_symbol":"RNA5SP94","gene_name":"RNA, 5S ribosomal pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:42892]","synonyms":"RN5S94","biotype":"rRNA","ncbi_id":"100873327","summary":null,"start":59694762,"end":59694869,"strand":1,"description":"RNA, 5S ribosomal pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:42892]"}, {"versioned_ensembl_gene_id":"ENSG00000274708.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54882533,"end":54882639,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207151.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11116092,"end":11116193,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200462.1","gene_symbol":"RNU6-727P","gene_name":"RNA, U6 small nuclear 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:47690]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481409","summary":null,"start":87420341,"end":87420447,"strand":-1,"description":"RNA, U6 small nuclear 727, pseudogene [Source:HGNC Symbol;Acc:HGNC:47690]"}, {"versioned_ensembl_gene_id":"ENSG00000201786.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153266909,"end":153267010,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252948.1","gene_symbol":"RNU6-1314P","gene_name":"RNA, U6 small nuclear 1314, pseudogene [Source:HGNC Symbol;Acc:HGNC:48277]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481595","summary":null,"start":26360989,"end":26361092,"strand":1,"description":"RNA, U6 small nuclear 1314, pseudogene [Source:HGNC Symbol;Acc:HGNC:48277]"}, {"versioned_ensembl_gene_id":"ENSG00000212553.1","gene_symbol":"SNORD116","gene_name":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":39857135,"end":39857227,"strand":-1,"description":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]"}, {"versioned_ensembl_gene_id":"ENSG00000240847.3","gene_symbol":"RN7SL497P","gene_name":"RNA, 7SL, cytoplasmic 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:46513]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481846","summary":null,"start":41191965,"end":41192265,"strand":-1,"description":"RNA, 7SL, cytoplasmic 497, pseudogene [Source:HGNC Symbol;Acc:HGNC:46513]"}, {"versioned_ensembl_gene_id":"ENSG00000252019.1","gene_symbol":"RNU6ATAC9P","gene_name":"RNA, U6atac small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:46908]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479547","summary":null,"start":54859215,"end":54859330,"strand":1,"description":"RNA, U6atac small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:46908]"}, {"versioned_ensembl_gene_id":"ENSG00000252069.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":109744643,"end":109744749,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281156.1","gene_symbol":"MIR3651","gene_name":"microRNA 3651 [Source:HGNC Symbol;Acc:HGNC:38897]","synonyms":"hsa-mir-3651","biotype":"miRNA","ncbi_id":"100500918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":92292458,"end":92292547,"strand":-1,"description":"microRNA 3651 [Source:HGNC Symbol;Acc:HGNC:38897]"}, {"versioned_ensembl_gene_id":"ENSG00000264041.2","gene_symbol":"RN7SL670P","gene_name":"RNA, 7SL, cytoplasmic 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:46686]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481105","summary":null,"start":203259604,"end":203259897,"strand":1,"description":"RNA, 7SL, cytoplasmic 670, pseudogene [Source:HGNC Symbol;Acc:HGNC:46686]"}, {"versioned_ensembl_gene_id":"ENSG00000223245.1","gene_symbol":"RNU4-63P","gene_name":"RNA, U4 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46999]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479587","summary":null,"start":41871271,"end":41871388,"strand":1,"description":"RNA, U4 small nuclear 63, pseudogene [Source:HGNC Symbol;Acc:HGNC:46999]"}, {"versioned_ensembl_gene_id":"ENSG00000238713.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":145149537,"end":145149649,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199856.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":7995570,"end":7995785,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000240106.2","gene_symbol":"RN7SL146P","gene_name":"RNA, 7SL, cytoplasmic 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:46162]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481827","summary":null,"start":16539688,"end":16539984,"strand":-1,"description":"RNA, 7SL, cytoplasmic 146, pseudogene [Source:HGNC Symbol;Acc:HGNC:46162]"}, {"versioned_ensembl_gene_id":"ENSG00000264901.1","gene_symbol":"MIR3616","gene_name":"microRNA 3616 [Source:HGNC Symbol;Acc:HGNC:38943]","synonyms":"hsa-mir-3616","biotype":"miRNA","ncbi_id":"100500814","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47166967,"end":47167058,"strand":1,"description":"microRNA 3616 [Source:HGNC Symbol;Acc:HGNC:38943]"}, {"versioned_ensembl_gene_id":"ENSG00000281877.2","gene_symbol":"RPS6KA1","gene_name":"ribosomal protein S6 kinase A1 [Source:HGNC Symbol;Acc:HGNC:10430]","synonyms":"RSK,p90Rsk,HU-1,RSK1","biotype":"protein_coding","ncbi_id":"6195","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 nonidentical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":26529761,"end":26575030,"strand":1,"description":"ribosomal protein S6 kinase A1 [Source:HGNC Symbol;Acc:HGNC:10430]"}, {"versioned_ensembl_gene_id":"ENSG00000252725.1","gene_symbol":"RNU6-765P","gene_name":"RNA, U6 small nuclear 765, pseudogene [Source:HGNC Symbol;Acc:HGNC:47728]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479905","summary":null,"start":38680006,"end":38680104,"strand":1,"description":"RNA, U6 small nuclear 765, pseudogene [Source:HGNC Symbol;Acc:HGNC:47728]"}, {"versioned_ensembl_gene_id":"ENSG00000207130.1","gene_symbol":"SNORA24","gene_name":"Small nucleolar RNA SNORA24 [Source:RFAM;Acc:RF00399]","synonyms":"SNORA24A,ACA24","biotype":"snoRNA","ncbi_id":"677809","summary":null,"start":128714571,"end":128714705,"strand":-1,"description":"Small nucleolar RNA SNORA24 [Source:RFAM;Acc:RF00399]"}, {"versioned_ensembl_gene_id":"ENSG00000238372.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":101847256,"end":101847360,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000223327.1","gene_symbol":"RNU2-71P","gene_name":"RNA, U2 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:48564]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480228","summary":null,"start":80585585,"end":80585773,"strand":-1,"description":"RNA, U2 small nuclear 71, pseudogene [Source:HGNC Symbol;Acc:HGNC:48564]"}, {"versioned_ensembl_gene_id":"ENSG00000207255.1","gene_symbol":"RNU6-1117P","gene_name":"RNA, U6 small nuclear 1117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48080]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481532","summary":null,"start":35471605,"end":35471708,"strand":1,"description":"RNA, U6 small nuclear 1117, pseudogene [Source:HGNC Symbol;Acc:HGNC:48080]"}, {"versioned_ensembl_gene_id":"ENSG00000252479.1","gene_symbol":"RNA5SP309","gene_name":"RNA, 5S ribosomal pseudogene 309 [Source:HGNC Symbol;Acc:HGNC:43209]","synonyms":"RN5S309","biotype":"rRNA","ncbi_id":"100873583","summary":null,"start":31259599,"end":31259704,"strand":1,"description":"RNA, 5S ribosomal pseudogene 309 [Source:HGNC Symbol;Acc:HGNC:43209]"}, {"versioned_ensembl_gene_id":"ENSG00000275360.1","gene_symbol":"MIR6868","gene_name":"microRNA 6868 [Source:HGNC Symbol;Acc:HGNC:50096]","synonyms":"hsa-mir-6868","biotype":"miRNA","ncbi_id":"102466753","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76098019,"end":76098076,"strand":-1,"description":"microRNA 6868 [Source:HGNC Symbol;Acc:HGNC:50096]"}, {"versioned_ensembl_gene_id":"ENSG00000272458.1","gene_symbol":"MIR432","gene_name":"microRNA 432 [Source:HGNC Symbol;Acc:HGNC:32083]","synonyms":"MIRN432,hsa-mir-432","biotype":"miRNA","ncbi_id":"574451","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100884483,"end":100884576,"strand":1,"description":"microRNA 432 [Source:HGNC Symbol;Acc:HGNC:32083]"}, {"versioned_ensembl_gene_id":"ENSG00000276233.1","gene_symbol":"PART1_3","gene_name":"Prostate androgen-regulated transcript 1 conserved region 3 [Source:RFAM;Acc:RF02161]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":60546219,"end":60546349,"strand":1,"description":"Prostate androgen-regulated transcript 1 conserved region 3 [Source:RFAM;Acc:RF02161]"}, {"versioned_ensembl_gene_id":"ENSG00000266038.1","gene_symbol":"MIR4659A","gene_name":"microRNA 4659a [Source:HGNC Symbol;Acc:HGNC:41857]","synonyms":"hsa-mir-4659a","biotype":"miRNA","ncbi_id":"100616348","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6745164,"end":6745244,"strand":1,"description":"microRNA 4659a [Source:HGNC Symbol;Acc:HGNC:41857]"}, {"versioned_ensembl_gene_id":"ENSG00000277446.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10691538,"end":10691831,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252353.1","gene_symbol":"RNU7-25P","gene_name":"RNA, U7 small nuclear 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:34121]","synonyms":"U7.25","biotype":"snRNA","ncbi_id":"100147812","summary":null,"start":3093568,"end":3093629,"strand":1,"description":"RNA, U7 small nuclear 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:34121]"}, {"versioned_ensembl_gene_id":"ENSG00000206589.1","gene_symbol":"RNU6-354P","gene_name":"RNA, U6 small nuclear 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:47317]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481290","summary":null,"start":43734179,"end":43734285,"strand":-1,"description":"RNA, U6 small nuclear 354, pseudogene [Source:HGNC Symbol;Acc:HGNC:47317]"}, {"versioned_ensembl_gene_id":"ENSG00000276706.1","gene_symbol":"VIS1","gene_name":"Viral integration site 1 [Source:RFAM;Acc:RF01992]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"7435","summary":null,"start":144705217,"end":144705419,"strand":1,"description":"Viral integration site 1 [Source:RFAM;Acc:RF01992]"}, {"versioned_ensembl_gene_id":"ENSG00000207768.3","gene_symbol":"MIR188","gene_name":"microRNA 188 [Source:HGNC Symbol;Acc:HGNC:31559]","synonyms":"hsa-mir-188,MIRN188","biotype":"miRNA","ncbi_id":"406964","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50003503,"end":50003588,"strand":1,"description":"microRNA 188 [Source:HGNC Symbol;Acc:HGNC:31559]"}, {"versioned_ensembl_gene_id":"ENSG00000281780.1","gene_symbol":"snoZ196","gene_name":"Small nucleolar RNA Z196/R39/R59 family [Source:RFAM;Acc:RF00134]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":206161841,"end":206161929,"strand":1,"description":"Small nucleolar RNA Z196/R39/R59 family [Source:RFAM;Acc:RF00134]"}, {"versioned_ensembl_gene_id":"ENSG00000283858.1","gene_symbol":"MIR3674","gene_name":"microRNA 3674 [Source:HGNC Symbol;Acc:HGNC:38915]","synonyms":"hsa-mir-3674","biotype":"miRNA","ncbi_id":"100500912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1801125,"end":1801192,"strand":1,"description":"microRNA 3674 [Source:HGNC Symbol;Acc:HGNC:38915]"}, {"versioned_ensembl_gene_id":"ENSG00000265617.1","gene_symbol":"MIR548AG2","gene_name":"microRNA 548ag-2 [Source:HGNC Symbol;Acc:HGNC:41745]","synonyms":"hsa-mir-548ag-2","biotype":"miRNA","ncbi_id":"100616440","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60564562,"end":60564625,"strand":1,"description":"microRNA 548ag-2 [Source:HGNC Symbol;Acc:HGNC:41745]"}, {"versioned_ensembl_gene_id":"ENSG00000206983.1","gene_symbol":"RNU6-49P","gene_name":"RNA, U6 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:34293]","synonyms":"RNU6-49","biotype":"snRNA","ncbi_id":"106478923","summary":null,"start":37870109,"end":37870215,"strand":1,"description":"RNA, U6 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:34293]"}, {"versioned_ensembl_gene_id":"ENSG00000266852.2","gene_symbol":"MIR4482","gene_name":"microRNA 4482 [Source:HGNC Symbol;Acc:HGNC:41792]","synonyms":"MIR4482-1,hsa-mir-4482","biotype":"miRNA","ncbi_id":"100616323","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104268336,"end":104268405,"strand":-1,"description":"microRNA 4482 [Source:HGNC Symbol;Acc:HGNC:41792]"}, {"versioned_ensembl_gene_id":"ENSG00000206739.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":19045256,"end":19045367,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264377.1","gene_symbol":"MIR4671","gene_name":"microRNA 4671 [Source:HGNC Symbol;Acc:HGNC:41598]","synonyms":"hsa-mir-4671","biotype":"miRNA","ncbi_id":"100616380","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":234306467,"end":234306539,"strand":1,"description":"microRNA 4671 [Source:HGNC Symbol;Acc:HGNC:41598]"}, {"versioned_ensembl_gene_id":"ENSG00000207147.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":40513144,"end":40513279,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000212441.1","gene_symbol":"RNU6-1269P","gene_name":"RNA, U6 small nuclear 1269, pseudogene [Source:HGNC Symbol;Acc:HGNC:48232]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480119","summary":null,"start":40233923,"end":40234029,"strand":1,"description":"RNA, U6 small nuclear 1269, pseudogene [Source:HGNC Symbol;Acc:HGNC:48232]"}, {"versioned_ensembl_gene_id":"ENSG00000222363.1","gene_symbol":"RNU4-34P","gene_name":"RNA, U4 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46970]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480385","summary":null,"start":29388560,"end":29388683,"strand":1,"description":"RNA, U4 small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46970]"}, {"versioned_ensembl_gene_id":"ENSG00000275474.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55052029,"end":55070922,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000277722.1","gene_symbol":"AC012314.11","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000202398.1","gene_symbol":"RNU6-61P","gene_name":"RNA, U6 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:42551]","synonyms":"RNU6-61","biotype":"snRNA","ncbi_id":"106480435","summary":null,"start":80369426,"end":80369534,"strand":-1,"description":"RNA, U6 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:42551]"}, {"versioned_ensembl_gene_id":"ENSG00000263456.1","gene_symbol":"MIR5189","gene_name":"microRNA 5189 [Source:HGNC Symbol;Acc:HGNC:43515]","synonyms":"hsa-mir-5189","biotype":"miRNA","ncbi_id":"100847057","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88468918,"end":88469031,"strand":1,"description":"microRNA 5189 [Source:HGNC Symbol;Acc:HGNC:43515]"}, {"versioned_ensembl_gene_id":"ENSG00000278040.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75016681,"end":75016848,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000238709.1","gene_symbol":"RNU7-56P","gene_name":"RNA, U7 small nuclear 56 pseudogene [Source:HGNC Symbol;Acc:HGNC:34152]","synonyms":"U7.56","biotype":"snRNA","ncbi_id":"100151651","summary":null,"start":16767844,"end":16767905,"strand":1,"description":"RNA, U7 small nuclear 56 pseudogene [Source:HGNC Symbol;Acc:HGNC:34152]"}, {"versioned_ensembl_gene_id":"ENSG00000263890.1","gene_symbol":"MIR4303","gene_name":"microRNA 4303 [Source:HGNC Symbol;Acc:HGNC:38256]","synonyms":"hsa-mir-4303","biotype":"miRNA","ncbi_id":"100422924","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97995383,"end":97995448,"strand":-1,"description":"microRNA 4303 [Source:HGNC Symbol;Acc:HGNC:38256]"}, {"versioned_ensembl_gene_id":"ENSG00000266052.1","gene_symbol":"MIR4500","gene_name":"microRNA 4500 [Source:HGNC Symbol;Acc:HGNC:41853]","synonyms":"hsa-mir-4500","biotype":"miRNA","ncbi_id":"100616182","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87618665,"end":87618740,"strand":-1,"description":"microRNA 4500 [Source:HGNC Symbol;Acc:HGNC:41853]"}, {"versioned_ensembl_gene_id":"ENSG00000277846.1","gene_symbol":"SNORD30","gene_name":"small nucleolar RNA, C/D box 30 [Source:HGNC Symbol;Acc:HGNC:10157]","synonyms":"RNU30,U30","biotype":"snoRNA","ncbi_id":"9299","summary":null,"start":62853663,"end":62853732,"strand":-1,"description":"small nucleolar RNA, C/D box 30 [Source:HGNC Symbol;Acc:HGNC:10157]"}, {"versioned_ensembl_gene_id":"ENSG00000212258.1","gene_symbol":"RNA5SP176","gene_name":"RNA, 5S ribosomal pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:43076]","synonyms":"RN5S176","biotype":"rRNA","ncbi_id":"100873438","summary":null,"start":7047227,"end":7047336,"strand":1,"description":"RNA, 5S ribosomal pseudogene 176 [Source:HGNC Symbol;Acc:HGNC:43076]"}, {"versioned_ensembl_gene_id":"ENSG00000241568.3","gene_symbol":"RN7SL338P","gene_name":"RNA, 7SL, cytoplasmic 338, pseudogene [Source:HGNC Symbol;Acc:HGNC:46354]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479347","summary":null,"start":35049271,"end":35049563,"strand":1,"description":"RNA, 7SL, cytoplasmic 338, pseudogene [Source:HGNC Symbol;Acc:HGNC:46354]"}, {"versioned_ensembl_gene_id":"ENSG00000276489.1","gene_symbol":"MIR6829","gene_name":"microRNA 6829 [Source:HGNC Symbol;Acc:HGNC:50055]","synonyms":"hsa-mir-6829","biotype":"miRNA","ncbi_id":"102465977","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":195882329,"end":195882395,"strand":-1,"description":"microRNA 6829 [Source:HGNC Symbol;Acc:HGNC:50055]"}, {"versioned_ensembl_gene_id":"ENSG00000207944.1","gene_symbol":"MIR574","gene_name":"microRNA 574 [Source:HGNC Symbol;Acc:HGNC:32830]","synonyms":"MIRN574,hsa-mir-574","biotype":"miRNA","ncbi_id":"693159","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38868032,"end":38868127,"strand":1,"description":"microRNA 574 [Source:HGNC Symbol;Acc:HGNC:32830]"}, {"versioned_ensembl_gene_id":"ENSG00000170458.13","gene_symbol":"CD14","gene_name":"CD14 molecule [Source:HGNC Symbol;Acc:HGNC:1628]","synonyms":null,"biotype":"protein_coding","ncbi_id":"929","summary":"The protein encoded by this gene is a surface antigen that is preferentially expressed on monocytes/macrophages. It cooperates with other proteins to mediate the innate immune response to bacterial lipopolysaccharide, and to viruses. This gene has been identified as a target candidate in the treatment of SARS-CoV-2-infected patients to potentially lessen or inhibit a severe inflammatory response. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2020]","start":140631728,"end":140633701,"strand":-1,"description":"CD14 molecule [Source:HGNC Symbol;Acc:HGNC:1628]"}, {"versioned_ensembl_gene_id":"ENSG00000265598.1","gene_symbol":"MIR5707","gene_name":"microRNA 5707 [Source:HGNC Symbol;Acc:HGNC:43449]","synonyms":"hsa-mir-5707","biotype":"miRNA","ncbi_id":"100847032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":158591616,"end":158591696,"strand":1,"description":"microRNA 5707 [Source:HGNC Symbol;Acc:HGNC:43449]"}, {"versioned_ensembl_gene_id":"ENSG00000252116.1","gene_symbol":"RNU4ATAC4P","gene_name":"RNA, U4atac small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:46890]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479539","summary":null,"start":67267601,"end":67267726,"strand":-1,"description":"RNA, U4atac small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:46890]"}, {"versioned_ensembl_gene_id":"ENSG00000240502.2","gene_symbol":"RN7SL837P","gene_name":"RNA, 7SL, cytoplasmic 837, pseudogene [Source:HGNC Symbol;Acc:HGNC:46853]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480536","summary":null,"start":230894141,"end":230894427,"strand":1,"description":"RNA, 7SL, cytoplasmic 837, pseudogene [Source:HGNC Symbol;Acc:HGNC:46853]"}, {"versioned_ensembl_gene_id":"ENSG00000201155.1","gene_symbol":"RNU1-24P","gene_name":"RNA, U1 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:42504]","synonyms":"U1.41","biotype":"snRNA","ncbi_id":"100873865","summary":null,"start":101778884,"end":101779048,"strand":-1,"description":"RNA, U1 small nuclear 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:42504]"}, {"versioned_ensembl_gene_id":"ENSG00000206611.1","gene_symbol":"SNORD24","gene_name":"small nucleolar RNA, C/D box 24 [Source:HGNC Symbol;Acc:HGNC:10146]","synonyms":"U24,RNU24","biotype":"snoRNA","ncbi_id":"26820","summary":null,"start":133349396,"end":133349470,"strand":1,"description":"small nucleolar RNA, C/D box 24 [Source:HGNC Symbol;Acc:HGNC:10146]"}, {"versioned_ensembl_gene_id":"ENSG00000276610.1","gene_symbol":"SNORD64","gene_name":"small nucleolar RNA, C/D box 64 [Source:HGNC Symbol;Acc:HGNC:32725]","synonyms":"HBII-13","biotype":"snoRNA","ncbi_id":"347686","summary":"This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]","start":24985100,"end":24985166,"strand":1,"description":"small nucleolar RNA, C/D box 64 [Source:HGNC Symbol;Acc:HGNC:32725]"}, {"versioned_ensembl_gene_id":"ENSG00000252001.1","gene_symbol":"RNA5SP303","gene_name":"RNA, 5S ribosomal pseudogene 303 [Source:HGNC Symbol;Acc:HGNC:43203]","synonyms":"RN5S303","biotype":"rRNA","ncbi_id":"100873577","summary":null,"start":19633683,"end":19633812,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 303 [Source:HGNC Symbol;Acc:HGNC:43203]"}, {"versioned_ensembl_gene_id":"ENSG00000238456.1","gene_symbol":"RNU6-1014P","gene_name":"RNA, U6 small nuclear 1014, pseudogene [Source:HGNC Symbol;Acc:HGNC:47977]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480013","summary":null,"start":46660658,"end":46660760,"strand":1,"description":"RNA, U6 small nuclear 1014, pseudogene [Source:HGNC Symbol;Acc:HGNC:47977]"}, {"versioned_ensembl_gene_id":"ENSG00000221614.1","gene_symbol":"MIR1185-2","gene_name":"microRNA 1185-2 [Source:HGNC Symbol;Acc:HGNC:35254]","synonyms":"hsa-mir-1185-2,MIRN1185-2","biotype":"miRNA","ncbi_id":"100302209","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101044198,"end":101044283,"strand":1,"description":"microRNA 1185-2 [Source:HGNC Symbol;Acc:HGNC:35254]"}, {"versioned_ensembl_gene_id":"ENSG00000252355.1","gene_symbol":"RN7SKP287","gene_name":"RNA, 7SK small nuclear pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:46011]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480921","summary":null,"start":43435132,"end":43435397,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 287 [Source:HGNC Symbol;Acc:HGNC:46011]"}, {"versioned_ensembl_gene_id":"ENSG00000283840.1","gene_symbol":"MIR6764","gene_name":"microRNA 6764 [Source:HGNC Symbol;Acc:HGNC:49994]","synonyms":"hsa-mir-6764","biotype":"miRNA","ncbi_id":"102466730","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100277357,"end":100277417,"strand":1,"description":"microRNA 6764 [Source:HGNC Symbol;Acc:HGNC:49994]"}, {"versioned_ensembl_gene_id":"ENSG00000276383.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30051467,"end":30051570,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000222560.1","gene_symbol":"RNU4-43P","gene_name":"RNA, U4 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46979]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481185","summary":null,"start":26012889,"end":26013025,"strand":1,"description":"RNA, U4 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:46979]"}, {"versioned_ensembl_gene_id":"ENSG00000251744.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":139108430,"end":139108534,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000265272.2","gene_symbol":"RN7SL693P","gene_name":"RNA, 7SL, cytoplasmic 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:46709]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479477","summary":null,"start":58490797,"end":58491075,"strand":1,"description":"RNA, 7SL, cytoplasmic 693, pseudogene [Source:HGNC Symbol;Acc:HGNC:46709]"}, {"versioned_ensembl_gene_id":"ENSG00000275480.1","gene_symbol":"AC131055.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22567423,"end":22568713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264316.1","gene_symbol":"MTCO3P13","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52043]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075224","summary":null,"start":22530612,"end":22531392,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52043]"}, {"versioned_ensembl_gene_id":"ENSG00000100483.13","gene_symbol":"VCPKMT","gene_name":"valosin containing protein lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:20352]","synonyms":"VCP-KMT,METTL21D,C14orf138","biotype":"protein_coding","ncbi_id":"79609","summary":null,"start":50108632,"end":50116600,"strand":-1,"description":"valosin containing protein lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:20352]"}, {"versioned_ensembl_gene_id":"ENSG00000198887.8","gene_symbol":"SMC5","gene_name":"structural maintenance of chromosomes 5 [Source:HGNC Symbol;Acc:HGNC:20465]","synonyms":"SMC5L1,KIAA0594","biotype":"protein_coding","ncbi_id":"23137","summary":null,"start":70258962,"end":70354888,"strand":1,"description":"structural maintenance of chromosomes 5 [Source:HGNC Symbol;Acc:HGNC:20465]"}, {"versioned_ensembl_gene_id":"ENSG00000274421.1","gene_symbol":"AL162390.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70310875,"end":70312120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212719.10","gene_symbol":"C17orf51","gene_name":"chromosome 17 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:27904]","synonyms":"FLJ33618,FLJ31874,FLJ12977","biotype":"protein_coding","ncbi_id":"339263","summary":null,"start":21524790,"end":21574458,"strand":-1,"description":"chromosome 17 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:27904]"}, {"versioned_ensembl_gene_id":"ENSG00000244582.2","gene_symbol":"AC233702.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21504558,"end":21505059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173898.11","gene_symbol":"SPTBN2","gene_name":"spectrin beta, non-erythrocytic 2 [Source:HGNC Symbol;Acc:HGNC:11276]","synonyms":"SCA5","biotype":"protein_coding","ncbi_id":"6712","summary":"Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009]","start":66685248,"end":66729226,"strand":-1,"description":"spectrin beta, non-erythrocytic 2 [Source:HGNC Symbol;Acc:HGNC:11276]"}, {"versioned_ensembl_gene_id":"ENSG00000113141.17","gene_symbol":"IK","gene_name":"IK cytokine, down-regulator of HLA II [Source:HGNC Symbol;Acc:HGNC:5958]","synonyms":"RER,RED","biotype":"protein_coding","ncbi_id":"3550","summary":"The protein encoded by this gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. Its function is unknown. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2. [provided by RefSeq, Jul 2008]","start":140647058,"end":140662479,"strand":1,"description":"IK cytokine, down-regulator of HLA II [Source:HGNC Symbol;Acc:HGNC:5958]"}, {"versioned_ensembl_gene_id":"ENSG00000143845.14","gene_symbol":"ETNK2","gene_name":"ethanolamine kinase 2 [Source:HGNC Symbol;Acc:HGNC:25575]","synonyms":"EKI2,FLJ10761","biotype":"protein_coding","ncbi_id":"55224","summary":"The protein encoded by this gene is a member of choline/ethanolamine kinase family which catalyzes the first step of phosphatidylethanolamine (PtdEtn) biosynthesis via the cytidine diphosphate (CDP) ethanolamine pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":204131062,"end":204152003,"strand":-1,"description":"ethanolamine kinase 2 [Source:HGNC Symbol;Acc:HGNC:25575]"}, {"versioned_ensembl_gene_id":"ENSG00000074582.12","gene_symbol":"BCS1L","gene_name":"BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [Source:HGNC Symbol;Acc:HGNC:1020]","synonyms":"Hs.6719,h-BCS,BJS,BCS","biotype":"protein_coding","ncbi_id":"617","summary":"This gene encodes a homolog of the S. cerevisiae bcs1 protein which is involved in the assembly of complex III of the mitochondrial respiratory chain. The encoded protein does not contain a mitochondrial targeting sequence but experimental studies confirm that it is imported into mitochondria. Mutations in this gene are associated with mitochondrial complex III deficiency and the GRACILE syndrome. Several alternatively spliced transcripts encoding two different isoforms have been described. [provided by RefSeq, Jan 2016]","start":218658764,"end":218663443,"strand":1,"description":"BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [Source:HGNC Symbol;Acc:HGNC:1020]"}, {"versioned_ensembl_gene_id":"ENSG00000183684.7","gene_symbol":"ALYREF","gene_name":"Aly/REF export factor [Source:HGNC Symbol;Acc:HGNC:19071]","synonyms":"THOC4,REF,BEF,ALY/REF,ALY","biotype":"protein_coding","ncbi_id":"10189","summary":"The protein encoded by this gene is a heat stable, nuclear protein and functions as a molecular chaperone. It is thought to regulate dimerization, DNA binding, and transcriptional activity of basic region-leucine zipper (bZIP) proteins. [provided by RefSeq, Jul 2008]","start":81887844,"end":81891586,"strand":-1,"description":"Aly/REF export factor [Source:HGNC Symbol;Acc:HGNC:19071]"}, {"versioned_ensembl_gene_id":"ENSG00000255129.5","gene_symbol":"AP000880.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113278437,"end":113314437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109016.17","gene_symbol":"DHRS7B","gene_name":"dehydrogenase/reductase 7B [Source:HGNC Symbol;Acc:HGNC:24547]","synonyms":"SDR32C1,MGC8916,DKFZp566O084,CGI-93","biotype":"protein_coding","ncbi_id":"25979","summary":"This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]","start":21123364,"end":21193265,"strand":1,"description":"dehydrogenase/reductase 7B [Source:HGNC Symbol;Acc:HGNC:24547]"}, {"versioned_ensembl_gene_id":"ENSG00000248643.5","gene_symbol":"RBM14-RBM4","gene_name":"RBM14-RBM4 readthrough [Source:HGNC Symbol;Acc:HGNC:38840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526737","summary":"This locus represents naturally occurring read-through transcription between the neighboring RBM14 (RNA binding motif protein 14) and RBM4 (RNA binding motif protein 4) genes. Alternative splicing results in multiple transcript variants, one of which encodes a fusion protein that shares sequence identity with each individual gene product. This fusion protein contains RRM and zinc finger domains, and it functions to stimulate transcription in a hormone and receptor-dependent manner. [provided by RefSeq, Nov 2010]","start":66616626,"end":66646469,"strand":1,"description":"RBM14-RBM4 readthrough [Source:HGNC Symbol;Acc:HGNC:38840]"}, {"versioned_ensembl_gene_id":"ENSG00000142546.13","gene_symbol":"NOSIP","gene_name":"nitric oxide synthase interacting protein [Source:HGNC Symbol;Acc:HGNC:17946]","synonyms":"CGI-25","biotype":"protein_coding","ncbi_id":"51070","summary":"The protein encoded by this gene may modulate the activity and localization of nitric oxide synthase (endothelial and neuronal) and thus nitric oxide production. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Aug 2012]","start":49555711,"end":49590262,"strand":-1,"description":"nitric oxide synthase interacting protein [Source:HGNC Symbol;Acc:HGNC:17946]"}, {"versioned_ensembl_gene_id":"ENSG00000225338.1","gene_symbol":"RPL23AP18","gene_name":"ribosomal protein L23a pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36726]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728134","summary":null,"start":212309051,"end":212309518,"strand":-1,"description":"ribosomal protein L23a pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36726]"}, {"versioned_ensembl_gene_id":"ENSG00000239306.4","gene_symbol":"RBM14","gene_name":"RNA binding motif protein 14 [Source:HGNC Symbol;Acc:HGNC:14219]","synonyms":"SYTIP1,SIP,DKFZp779J0927,COAA","biotype":"protein_coding","ncbi_id":"10432","summary":"This gene encodes a ribonucleoprotein that functions as a general nuclear coactivator, and an RNA splicing modulator. This protein contains two RNA recognition motifs (RRM) at the N-terminus, and multiple hexapeptide repeat domain at the C-terminus that interacts with thyroid hormone receptor-binding protein (TRBP), and is required for transcription activation. Alternatively spliced transcript variants encoding different isoforms (with opposing effects on transcription) have been described for this gene. [provided by RefSeq, Oct 2011]","start":66616582,"end":66627347,"strand":1,"description":"RNA binding motif protein 14 [Source:HGNC Symbol;Acc:HGNC:14219]"}, {"versioned_ensembl_gene_id":"ENSG00000270333.1","gene_symbol":"AL390123.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109661814,"end":109662050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100612.13","gene_symbol":"DHRS7","gene_name":"dehydrogenase/reductase 7 [Source:HGNC Symbol;Acc:HGNC:21524]","synonyms":"SDR34C1,retDSR4","biotype":"protein_coding","ncbi_id":"51635","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family, which has over 46,000 members. Members in this family are enzymes that metabolize many different compounds, such as steroid hormones, prostaglandins, retinoids, lipids and xenobiotics. [provided by RefSeq, Apr 2016]","start":60144120,"end":60169856,"strand":-1,"description":"dehydrogenase/reductase 7 [Source:HGNC Symbol;Acc:HGNC:21524]"}, {"versioned_ensembl_gene_id":"ENSG00000203434.2","gene_symbol":"AL353740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108547975,"end":108561815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166165.12","gene_symbol":"CKB","gene_name":"creatine kinase B [Source:HGNC Symbol;Acc:HGNC:1991]","synonyms":"CKBB","biotype":"protein_coding","ncbi_id":"1152","summary":"The protein encoded by this gene is a cytoplasmic enzyme involved in energy homeostasis. The encoded protein reversibly catalyzes the transfer of phosphate between ATP and various phosphogens such as creatine phosphate. It acts as a homodimer in brain as well as in other tissues, and as a heterodimer with a similar muscle isozyme in heart. The encoded protein is a member of the ATP:guanido phosphotransferase protein family. A pseudogene of this gene has been characterized. [provided by RefSeq, Jul 2008]","start":103519659,"end":103523111,"strand":-1,"description":"creatine kinase B [Source:HGNC Symbol;Acc:HGNC:1991]"}, {"versioned_ensembl_gene_id":"ENSG00000277213.1","gene_symbol":"SDR42E1P2","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51833]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422346","summary":null,"start":42408526,"end":42409006,"strand":-1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51833]"}, {"versioned_ensembl_gene_id":"ENSG00000097007.17","gene_symbol":"ABL1","gene_name":"ABL proto-oncogene 1, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:76]","synonyms":"p150,JTK7,c-ABL,ABL","biotype":"protein_coding","ncbi_id":"25","summary":"This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA-binding activity that is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function. This gene has been found fused to a variety of translocation partner genes in various leukemias, most notably the t(9;22) translocation that results in a fusion with the 5' end of the breakpoint cluster region gene (BCR; MIM:151410). Alternative splicing of this gene results in two transcript variants, which contain alternative first exons that are spliced to the remaining common exons. [provided by RefSeq, Aug 2014]","start":130713946,"end":130887675,"strand":1,"description":"ABL proto-oncogene 1, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:76]"}, {"versioned_ensembl_gene_id":"ENSG00000130713.15","gene_symbol":"EXOSC2","gene_name":"exosome component 2 [Source:HGNC Symbol;Acc:HGNC:17097]","synonyms":"p7,hRrp4p,Rrp4p,RRP4","biotype":"protein_coding","ncbi_id":"23404","summary":null,"start":130693721,"end":130704894,"strand":1,"description":"exosome component 2 [Source:HGNC Symbol;Acc:HGNC:17097]"}, {"versioned_ensembl_gene_id":"ENSG00000227487.3","gene_symbol":"NCAM1-AS1","gene_name":"NCAM1 antisense RNA1 [Source:HGNC Symbol;Acc:HGNC:48675]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288346","summary":null,"start":113269532,"end":113273901,"strand":-1,"description":"NCAM1 antisense RNA1 [Source:HGNC Symbol;Acc:HGNC:48675]"}, {"versioned_ensembl_gene_id":"ENSG00000182676.4","gene_symbol":"PPP1R27","gene_name":"protein phosphatase 1 regulatory subunit 27 [Source:HGNC Symbol;Acc:HGNC:16813]","synonyms":"toonin,DYSFIP1","biotype":"protein_coding","ncbi_id":"116729","summary":null,"start":81833492,"end":81835050,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 27 [Source:HGNC Symbol;Acc:HGNC:16813]"}, {"versioned_ensembl_gene_id":"ENSG00000185504.16","gene_symbol":"FAAP100","gene_name":"Fanconi anemia core complex associated protein 100 [Source:HGNC Symbol;Acc:HGNC:26171]","synonyms":"FLJ22175,C17orf70","biotype":"protein_coding","ncbi_id":"80233","summary":"FAAP100 is a component of the Fanconi anemia (FA; MIM 277650) core complex and is required for core complex stability and FANCD2 (see MIM 227646) monoubiquitination (Ling et al., 2007 [PubMed 17396147]).[supplied by OMIM, Mar 2008]","start":81539885,"end":81553961,"strand":-1,"description":"Fanconi anemia core complex associated protein 100 [Source:HGNC Symbol;Acc:HGNC:26171]"}, {"versioned_ensembl_gene_id":"ENSG00000226981.2","gene_symbol":"ABHD17AP6","gene_name":"abhydrolase domain containing 17A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34044]","synonyms":"FAM108A7P","biotype":"unprocessed_pseudogene","ncbi_id":"644988","summary":null,"start":20814620,"end":20844257,"strand":1,"description":"abhydrolase domain containing 17A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34044]"}, {"versioned_ensembl_gene_id":"ENSG00000265790.1","gene_symbol":"AC090774.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20901939,"end":20902680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157111.12","gene_symbol":"TMEM171","gene_name":"transmembrane protein 171 [Source:HGNC Symbol;Acc:HGNC:27031]","synonyms":"PRP2","biotype":"protein_coding","ncbi_id":"134285","summary":null,"start":73120292,"end":73131817,"strand":1,"description":"transmembrane protein 171 [Source:HGNC Symbol;Acc:HGNC:27031]"}, {"versioned_ensembl_gene_id":"ENSG00000130244.12","gene_symbol":"FAM98C","gene_name":"family with sequence similarity 98 member C [Source:HGNC Symbol;Acc:HGNC:27119]","synonyms":"FLJ44669","biotype":"protein_coding","ncbi_id":"147965","summary":null,"start":38403135,"end":38409088,"strand":1,"description":"family with sequence similarity 98 member C [Source:HGNC Symbol;Acc:HGNC:27119]"}, {"versioned_ensembl_gene_id":"ENSG00000131400.7","gene_symbol":"NAPSA","gene_name":"napsin A aspartic peptidase [Source:HGNC Symbol;Acc:HGNC:13395]","synonyms":"KAP,NAPA,NAP1,Kdap","biotype":"protein_coding","ncbi_id":"9476","summary":"This gene encodes a member of the peptidase A1 family of aspartic proteases. The encoded preproprotein is proteolytically processed to generate an activation peptide and the mature protease. The activation peptides of aspartic proteinases function as inhibitors of the protease active site. These peptide segments, or pro-parts, are deemed important for correct folding, targeting, and control of the activation of aspartic proteinase zymogens. The encoded protease may play a role in the proteolytic processing of pulmonary surfactant protein B in the lung and may function in protein catabolism in the renal proximal tubules. This gene has been described as a marker for lung adenocarcinoma and renal cell carcinoma. [provided by RefSeq, Feb 2016]","start":50358477,"end":50365830,"strand":-1,"description":"napsin A aspartic peptidase [Source:HGNC Symbol;Acc:HGNC:13395]"}, {"versioned_ensembl_gene_id":"ENSG00000254844.4","gene_symbol":"AP000757.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117818443,"end":117821992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100749.7","gene_symbol":"VRK1","gene_name":"vaccinia related kinase 1 [Source:HGNC Symbol;Acc:HGNC:12718]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7443","summary":"This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. This gene is widely expressed in human tissues and has increased expression in actively dividing cells, such as those in testis, thymus, fetal liver, and carcinomas. Its protein localizes to the nucleus and has been shown to promote the stability and nuclear accumulation of a transcriptionally active p53 molecule and, in vitro, to phosphorylate Thr18 of p53 and reduce p53 ubiquitination. This gene, therefore, may regulate cell proliferation. This protein also phosphorylates histone, casein, and the transcription factors ATF2 (activating transcription factor 2) and c-JUN. [provided by RefSeq, Jul 2008]","start":96797304,"end":96931722,"strand":1,"description":"vaccinia related kinase 1 [Source:HGNC Symbol;Acc:HGNC:12718]"}, {"versioned_ensembl_gene_id":"ENSG00000270403.1","gene_symbol":"AP001554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117668483,"end":117668858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181409.11","gene_symbol":"AATK","gene_name":"apoptosis associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:21]","synonyms":"AATYK,PPP1R77,LMTK1,LMR1,KIAA0641,AATYK1","biotype":"protein_coding","ncbi_id":"9625","summary":"The protein encoded by this gene contains a tyrosine kinase domain at the N-terminus and a proline-rich domain at the C-terminus. This gene is induced during apoptosis, and expression of this gene may be a necessary pre-requisite for the induction of growth arrest and/or apoptosis of myeloid precursor cells. This gene has been shown to produce neuronal differentiation in a neuroblastoma cell line. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":81117295,"end":81166077,"strand":-1,"description":"apoptosis associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:21]"}, {"versioned_ensembl_gene_id":"ENSG00000267638.1","gene_symbol":"AC023855.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44115912,"end":44120595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271926.1","gene_symbol":"AC008972.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72953635,"end":72954274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184254.16","gene_symbol":"ALDH1A3","gene_name":"aldehyde dehydrogenase 1 family member A3 [Source:HGNC Symbol;Acc:HGNC:409]","synonyms":"ALDH6,RALDH3","biotype":"protein_coding","ncbi_id":"220","summary":"This gene encodes an aldehyde dehydrogenase enzyme that uses retinal as a substrate. Mutations in this gene have been associated with microphthalmia, isolated 8, and expression changes have also been detected in tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":100877714,"end":100916626,"strand":1,"description":"aldehyde dehydrogenase 1 family member A3 [Source:HGNC Symbol;Acc:HGNC:409]"}, {"versioned_ensembl_gene_id":"ENSG00000176108.9","gene_symbol":"CHMP6","gene_name":"charged multivesicular body protein 6 [Source:HGNC Symbol;Acc:HGNC:25675]","synonyms":"VPS20,FLJ11749","biotype":"protein_coding","ncbi_id":"79643","summary":"This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein family. Proteins in this family are part of the ESCRT-III (endosomal sorting complex required for transport III) which degrades surface receptors, and in biosynthesis of endosomes. [provided by RefSeq, Mar 2012]","start":80991598,"end":81009517,"strand":1,"description":"charged multivesicular body protein 6 [Source:HGNC Symbol;Acc:HGNC:25675]"}, {"versioned_ensembl_gene_id":"ENSG00000230088.1","gene_symbol":"KRT16P5","gene_name":"keratin 16 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"353196","summary":null,"start":20493634,"end":20494155,"strand":-1,"description":"keratin 16 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37810]"}, {"versioned_ensembl_gene_id":"ENSG00000229586.2","gene_symbol":"TNPO1P3","gene_name":"transportin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339257","summary":null,"start":20481330,"end":20483991,"strand":-1,"description":"transportin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50718]"}, {"versioned_ensembl_gene_id":"ENSG00000115556.13","gene_symbol":"PLCD4","gene_name":"phospholipase C delta 4 [Source:HGNC Symbol;Acc:HGNC:9062]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84812","summary":"This gene encodes a member of the delta class of phospholipase C enzymes. Phospholipase C enzymes play a critical role in many cellular processes by hydrolyzing phosphatidylinositol 4,5-bisphosphate into two intracellular second messengers, inositol 1,4,5-trisphosphate and diacylglycerol. Expression of this gene may be a marker for cancer. [provided by RefSeq, Jan 2011]","start":218607765,"end":218637184,"strand":1,"description":"phospholipase C delta 4 [Source:HGNC Symbol;Acc:HGNC:9062]"}, {"versioned_ensembl_gene_id":"ENSG00000117500.12","gene_symbol":"TMED5","gene_name":"transmembrane p24 trafficking protein 5 [Source:HGNC Symbol;Acc:HGNC:24251]","synonyms":"CGI-100,p24gamma2,p24g2","biotype":"protein_coding","ncbi_id":"50999","summary":null,"start":93149742,"end":93180728,"strand":-1,"description":"transmembrane p24 trafficking protein 5 [Source:HGNC Symbol;Acc:HGNC:24251]"}, {"versioned_ensembl_gene_id":"ENSG00000251613.3","gene_symbol":"AC063979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72687112,"end":72762727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187556.7","gene_symbol":"NANOS3","gene_name":"nanos C2HC-type zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:22048]","synonyms":"ZC2HC12C,NOS3,NANOS1L","biotype":"protein_coding","ncbi_id":"342977","summary":null,"start":13862063,"end":13880757,"strand":1,"description":"nanos C2HC-type zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:22048]"}, {"versioned_ensembl_gene_id":"ENSG00000184232.8","gene_symbol":"OAF","gene_name":"out at first homolog [Source:HGNC Symbol;Acc:HGNC:28752]","synonyms":"MGC52117","biotype":"protein_coding","ncbi_id":"220323","summary":null,"start":120210767,"end":120230332,"strand":1,"description":"out at first homolog [Source:HGNC Symbol;Acc:HGNC:28752]"}, {"versioned_ensembl_gene_id":"ENSG00000117505.12","gene_symbol":"DR1","gene_name":"down-regulator of transcription 1 [Source:HGNC Symbol;Acc:HGNC:3017]","synonyms":"NCB2,NC2B,NC2-BETA","biotype":"protein_coding","ncbi_id":"1810","summary":"This gene encodes a TBP- (TATA box-binding protein) associated phosphoprotein that represses both basal and activated levels of transcription. The encoded protein is phosphorylated in vivo and this phosphorylation affects its interaction with TBP. This protein contains a histone fold motif at the amino terminus, a TBP-binding domain, and a glutamine- and alanine-rich region. The binding of DR1 repressor complexes to TBP-promoter complexes may establish a mechanism in which an altered DNA conformation, together with the formation of higher order complexes, inhibits the assembly of the preinitiation complex and controls the rate of RNA polymerase II transcription. [provided by RefSeq, Jul 2008]","start":93345888,"end":93369498,"strand":1,"description":"down-regulator of transcription 1 [Source:HGNC Symbol;Acc:HGNC:3017]"}, {"versioned_ensembl_gene_id":"ENSG00000214922.9","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29726601,"end":29749049,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000228064.1","gene_symbol":"AC023469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150982506,"end":151003474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170279.2","gene_symbol":"C7orf33","gene_name":"chromosome 7 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:21724]","synonyms":null,"biotype":"protein_coding","ncbi_id":"202865","summary":null,"start":148590565,"end":148615860,"strand":1,"description":"chromosome 7 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:21724]"}, {"versioned_ensembl_gene_id":"ENSG00000222031.1","gene_symbol":"AC023469.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151001220,"end":151048774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238227.7","gene_symbol":"TMEM250","gene_name":"transmembrane protein 250 [Source:HGNC Symbol;Acc:HGNC:31009]","synonyms":"C9orf69,bA83N9.1","biotype":"protein_coding","ncbi_id":"90120","summary":null,"start":136114581,"end":136118863,"strand":-1,"description":"transmembrane protein 250 [Source:HGNC Symbol;Acc:HGNC:31009]"}, {"versioned_ensembl_gene_id":"ENSG00000196873.15","gene_symbol":"CBWD3","gene_name":"COBW domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18519]","synonyms":"bA561O23.1","biotype":"protein_coding","ncbi_id":"445571","summary":null,"start":68232003,"end":68300015,"strand":1,"description":"COBW domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18519]"}, {"versioned_ensembl_gene_id":"ENSG00000163072.15","gene_symbol":"NOSTRIN","gene_name":"nitric oxide synthase trafficking [Source:HGNC Symbol;Acc:HGNC:20203]","synonyms":"MGC20702","biotype":"protein_coding","ncbi_id":"115677","summary":"Nitric oxide (NO) is a potent mediator in biologic processes such as neurotransmission, inflammatory response, and vascular homeostasis. NOSTRIN binds the enzyme responsible for NO production, endothelial NO synthase (ENOS; MIM 163729), and triggers the translocation of ENOS from the plasma membrane to vesicle-like subcellular structures, thereby attenuating ENOS-dependent NO production.[supplied by OMIM, Apr 2004]","start":168786539,"end":168865514,"strand":1,"description":"nitric oxide synthase trafficking [Source:HGNC Symbol;Acc:HGNC:20203]"}, {"versioned_ensembl_gene_id":"ENSG00000167900.11","gene_symbol":"TK1","gene_name":"thymidine kinase 1 [Source:HGNC Symbol;Acc:HGNC:11830]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7083","summary":"The protein encoded by this gene is a cytosolic enzyme that catalyzes the addition of a gamma-phosphate group to thymidine. This creates dTMP and is the first step in the biosynthesis of dTTP, which is one component required for DNA replication. The encoded protein, whose levels fluctuate depending on the cell cycle stage, can act as a low activity dimer or a high activity tetramer. High levels of this protein have been used as a biomarker for diagnosing and categorizing many types of cancers. [provided by RefSeq, Oct 2016]","start":78174075,"end":78187233,"strand":-1,"description":"thymidine kinase 1 [Source:HGNC Symbol;Acc:HGNC:11830]"}, {"versioned_ensembl_gene_id":"ENSG00000235993.1","gene_symbol":"AC007559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":229701794,"end":229702148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187957.7","gene_symbol":"DNER","gene_name":"delta/notch like EGF repeat containing [Source:HGNC Symbol;Acc:HGNC:24456]","synonyms":"UNQ26,bet","biotype":"protein_coding","ncbi_id":"92737","summary":null,"start":229357629,"end":229714558,"strand":-1,"description":"delta/notch like EGF repeat containing [Source:HGNC Symbol;Acc:HGNC:24456]"}, {"versioned_ensembl_gene_id":"ENSG00000187997.11","gene_symbol":"C17orf99","gene_name":"chromosome 17 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:34490]","synonyms":"UNQ464,GLPG464","biotype":"protein_coding","ncbi_id":"100141515","summary":null,"start":78146353,"end":78166177,"strand":1,"description":"chromosome 17 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:34490]"}, {"versioned_ensembl_gene_id":"ENSG00000224014.1","gene_symbol":"AL390728.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247175256,"end":247175525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221953.5","gene_symbol":"C1orf229","gene_name":"chromosome 1 open reading frame 229 [Source:HGNC Symbol;Acc:HGNC:33759]","synonyms":"FLJ45717","biotype":"lincRNA","ncbi_id":"388759","summary":null,"start":247110160,"end":247112417,"strand":-1,"description":"chromosome 1 open reading frame 229 [Source:HGNC Symbol;Acc:HGNC:33759]"}, {"versioned_ensembl_gene_id":"ENSG00000269487.1","gene_symbol":"AC008635.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46728603,"end":46732700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179151.11","gene_symbol":"EDC3","gene_name":"enhancer of mRNA decapping 3 [Source:HGNC Symbol;Acc:HGNC:26114]","synonyms":"YJEFN2,YJDC,LSM16,hYjeF_N2-15q23,FLJ21128","biotype":"protein_coding","ncbi_id":"80153","summary":"This gene encodes a protein that is important in mRNA degradation. The encoded protein is a component of a decapping complex that promotes efficient removal of the monomethylguanosine (m7G) cap from mRNAs, as part of the 5' to 3' mRNA decay pathway. Mutations in this gene have been identified in human patients with an autosomal recessive form of intellectual disability. [provided by RefSeq, May 2017]","start":74630558,"end":74696292,"strand":-1,"description":"enhancer of mRNA decapping 3 [Source:HGNC Symbol;Acc:HGNC:26114]"}, {"versioned_ensembl_gene_id":"ENSG00000157654.17","gene_symbol":"PALM2-AKAP2","gene_name":"PALM2-AKAP2 readthrough [Source:HGNC Symbol;Acc:HGNC:33529]","synonyms":null,"biotype":"protein_coding","ncbi_id":"445815","summary":"This gene belongs to the paralemmin downstream gene (PDG) family defined in PMID:22855693. Paralemmin downstream genes may have evolved contiguously with the paralemmin genes and are associated with other paralemmin paralogs in humans and several other taxa. The gene encodes three distinct protein isoforms, the PALM2 isoform, the AKAP2 isoform and the PALM2-AKAP2 isoform. The biological significance of the PALM2-AKAP2 isoforms is yet unknown. Earlier, PALM2 and AKAP2 were annotated as separate genes and PALM2-AKAP2 was annotated as a readthrough gene. [provided by RefSeq, May 2019]","start":109780309,"end":110172512,"strand":1,"description":"PALM2-AKAP2 readthrough [Source:HGNC Symbol;Acc:HGNC:33529]"}, {"versioned_ensembl_gene_id":"ENSG00000248962.1","gene_symbol":"AC025773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4012708,"end":4013649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256441.1","gene_symbol":"AP001888.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69737298,"end":69738017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258592.1","gene_symbol":"AL391152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57066260,"end":57112660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260574.1","gene_symbol":"AL360157.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81969453,"end":81969539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224995.1","gene_symbol":"LINC01526","gene_name":"long intergenic non-protein coding RNA 1526 [Source:HGNC Symbol;Acc:HGNC:51265]","synonyms":"Lnc-FAM46A-1","biotype":"lincRNA","ncbi_id":"101928770","summary":null,"start":81813286,"end":81814157,"strand":-1,"description":"long intergenic non-protein coding RNA 1526 [Source:HGNC Symbol;Acc:HGNC:51265]"}, {"versioned_ensembl_gene_id":"ENSG00000231368.1","gene_symbol":"RPSAP40","gene_name":"ribosomal protein SA pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36828]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270917","summary":null,"start":148647707,"end":148648597,"strand":-1,"description":"ribosomal protein SA pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36828]"}, {"versioned_ensembl_gene_id":"ENSG00000279691.1","gene_symbol":"AC113410.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133052769,"end":133052971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277984.1","gene_symbol":"AP001264.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95057282,"end":95057984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124915.10","gene_symbol":"DKFZP434K028","gene_name":"uncharacterized LOC26070 [Source:NCBI gene;Acc:26070]","synonyms":null,"biotype":"lincRNA","ncbi_id":"26070","summary":null,"start":61746493,"end":61757655,"strand":-1,"description":"uncharacterized LOC26070 [Source:NCBI gene;Acc:26070]"}, {"versioned_ensembl_gene_id":"ENSG00000166197.16","gene_symbol":"NOLC1","gene_name":"nucleolar and coiled-body phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:15608]","synonyms":"P130,NOPP140,NOPP130,KIAA0035","biotype":"protein_coding","ncbi_id":"9221","summary":null,"start":102152176,"end":102163871,"strand":1,"description":"nucleolar and coiled-body phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:15608]"}, {"versioned_ensembl_gene_id":"ENSG00000149300.9","gene_symbol":"C11orf52","gene_name":"chromosome 11 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:30531]","synonyms":"MGC14839,FLJ25219","biotype":"protein_coding","ncbi_id":"91894","summary":null,"start":111918032,"end":111926872,"strand":1,"description":"chromosome 11 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:30531]"}, {"versioned_ensembl_gene_id":"ENSG00000185775.9","gene_symbol":"SPATA31A6","gene_name":"SPATA31 subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:32006]","synonyms":"OTTHUMG00000013224,FAM75A6","biotype":"protein_coding","ncbi_id":"389730","summary":null,"start":42183659,"end":42189882,"strand":1,"description":"SPATA31 subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:32006]"}, {"versioned_ensembl_gene_id":"ENSG00000220378.3","gene_symbol":"KRT8P42","gene_name":"keratin 8 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:39876]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418750","summary":null,"start":134296997,"end":134298695,"strand":-1,"description":"keratin 8 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:39876]"}, {"versioned_ensembl_gene_id":"ENSG00000188029.8","gene_symbol":"CTSL3P","gene_name":"cathepsin L family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33132]","synonyms":"HCTSL-s,CTSL3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"392360","summary":null,"start":87772453,"end":87786884,"strand":1,"description":"cathepsin L family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:33132]"}, {"versioned_ensembl_gene_id":"ENSG00000237747.1","gene_symbol":"AL160279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87741233,"end":87741953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242571.1","gene_symbol":"RPL21P11","gene_name":"ribosomal protein L21 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"157206","summary":null,"start":90366697,"end":90367179,"strand":-1,"description":"ribosomal protein L21 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19800]"}, {"versioned_ensembl_gene_id":"ENSG00000161905.12","gene_symbol":"ALOX15","gene_name":"arachidonate 15-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:433]","synonyms":"15-LOX-1","biotype":"protein_coding","ncbi_id":"246","summary":"This gene encodes a member of the lipoxygenase family of proteins. The encoded enzyme acts on various polyunsaturated fatty acid substrates to generate various bioactive lipid mediators such as eicosanoids, hepoxilins, lipoxins, and other molecules. The encoded enzyme and its reaction products have been shown to regulate inflammation and immunity. Multiple pseudogenes of this gene have been identified in the human genome. [provided by RefSeq, Aug 2017]","start":4630902,"end":4642294,"strand":-1,"description":"arachidonate 15-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:433]"}, {"versioned_ensembl_gene_id":"ENSG00000283594.1","gene_symbol":"FAM236C","gene_name":"family with sequence similarity 236 member C [Source:HGNC Symbol;Acc:HGNC:52641]","synonyms":null,"biotype":"protein_coding","ncbi_id":"109729126","summary":null,"start":72912615,"end":72913401,"strand":1,"description":"family with sequence similarity 236 member C [Source:HGNC Symbol;Acc:HGNC:52641]"}, {"versioned_ensembl_gene_id":"ENSG00000182492.15","gene_symbol":"BGN","gene_name":"biglycan [Source:HGNC Symbol;Acc:HGNC:1044]","synonyms":"SLRR1A,DSPG1","biotype":"protein_coding","ncbi_id":"633","summary":"This gene encodes a member of the small leucine-rich proteoglycan (SLRP) family of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein, which plays a role in bone growth, muscle development and regeneration, and collagen fibril assembly in multiple tissues. This protein may also regulate inflammation and innate immunity. Additionally, the encoded protein may contribute to atherosclerosis and aortic valve stenosis in human patients. This gene and the related gene decorin are thought to be the result of a gene duplication. [provided by RefSeq, Nov 2015]","start":153494939,"end":153509554,"strand":1,"description":"biglycan [Source:HGNC Symbol;Acc:HGNC:1044]"}, {"versioned_ensembl_gene_id":"ENSG00000179761.11","gene_symbol":"PIPOX","gene_name":"pipecolic acid and sarcosine oxidase [Source:HGNC Symbol;Acc:HGNC:17804]","synonyms":"LPIPOX","biotype":"protein_coding","ncbi_id":"51268","summary":null,"start":28950513,"end":29057220,"strand":1,"description":"pipecolic acid and sarcosine oxidase [Source:HGNC Symbol;Acc:HGNC:17804]"}, {"versioned_ensembl_gene_id":"ENSG00000263781.3","gene_symbol":"AC024619.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29021325,"end":29021640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258569.1","gene_symbol":"AC007376.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76710658,"end":76761388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226249.1","gene_symbol":"AL365271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147741434,"end":147743324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063015.19","gene_symbol":"SEZ6","gene_name":"seizure related 6 homolog [Source:HGNC Symbol;Acc:HGNC:15955]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124925","summary":"The protein encoded by this gene is thought to contain five cysteine-rich motifs that are similar to sushi domains, as well as two domains similar to the amino terminal half of the CUB (for complement C1r/C1s, Uegf, Bmp1) domain. Mutations in this gene have been associated with febrile seizures. [provided by RefSeq, Jul 2016]","start":28954901,"end":29006440,"strand":-1,"description":"seizure related 6 homolog [Source:HGNC Symbol;Acc:HGNC:15955]"}, {"versioned_ensembl_gene_id":"ENSG00000269815.1","gene_symbol":"AC010463.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17296196,"end":17296695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203727.3","gene_symbol":"SAMD5","gene_name":"sterile alpha motif domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21180]","synonyms":"dJ875H10.1","biotype":"protein_coding","ncbi_id":"389432","summary":null,"start":147508927,"end":147737547,"strand":1,"description":"sterile alpha motif domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21180]"}, {"versioned_ensembl_gene_id":"ENSG00000247400.3","gene_symbol":"DNAJC3-AS1","gene_name":"DNAJC3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39808]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289274","summary":null,"start":95648733,"end":95676925,"strand":-1,"description":"DNAJC3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39808]"}, {"versioned_ensembl_gene_id":"ENSG00000134255.13","gene_symbol":"CEPT1","gene_name":"choline/ethanolamine phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:24289]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10390","summary":"This gene codes for a choline/ethanolaminephosphotransferase, which functions in the synthesis of choline- or ethanolamine- containing phospholipids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":111139627,"end":111185102,"strand":1,"description":"choline/ethanolamine phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:24289]"}, {"versioned_ensembl_gene_id":"ENSG00000281641.2","gene_symbol":"SAMD12-AS1","gene_name":"SAMD12 antisense RNA 1 [Source:NCBI gene;Acc:552860]","synonyms":"NCRNA00252,C8orf26","biotype":"lincRNA","ncbi_id":"552860","summary":null,"start":118621001,"end":118858218,"strand":1,"description":"SAMD12 antisense RNA 1 [Source:NCBI gene;Acc:552860]"}, {"versioned_ensembl_gene_id":"ENSG00000127220.5","gene_symbol":"ABHD8","gene_name":"abhydrolase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23759]","synonyms":"MGC2512,MGC14280,FLJ11743","biotype":"protein_coding","ncbi_id":"79575","summary":"This gene is upstream of, and in a head-to-head orientation with the gene for the mitochondrial ribosomal protein L34. The predicted protein contains alpha/beta hydrolase fold and secretory lipase domains. [provided by RefSeq, Jul 2008]","start":17292131,"end":17310236,"strand":-1,"description":"abhydrolase domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23759]"}, {"versioned_ensembl_gene_id":"ENSG00000177570.13","gene_symbol":"SAMD12","gene_name":"sterile alpha motif domain containing 12 [Source:HGNC Symbol;Acc:HGNC:31750]","synonyms":"FLJ39458","biotype":"protein_coding","ncbi_id":"401474","summary":null,"start":118189459,"end":118621995,"strand":-1,"description":"sterile alpha motif domain containing 12 [Source:HGNC Symbol;Acc:HGNC:31750]"}, {"versioned_ensembl_gene_id":"ENSG00000253512.1","gene_symbol":"AC008562.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165782805,"end":165783134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253693.1","gene_symbol":"AC008415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165349030,"end":165778689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078795.16","gene_symbol":"PKD2L2","gene_name":"polycystin 2 like 2, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9012]","synonyms":"TRPP5","biotype":"protein_coding","ncbi_id":"27039","summary":null,"start":137887968,"end":137942747,"strand":1,"description":"polycystin 2 like 2, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9012]"}, {"versioned_ensembl_gene_id":"ENSG00000175470.18","gene_symbol":"PPP2R2D","gene_name":"protein phosphatase 2 regulatory subunit Bdelta [Source:HGNC Symbol;Acc:HGNC:23732]","synonyms":"MDS026,B55delta,B55D","biotype":"protein_coding","ncbi_id":"55844","summary":null,"start":131900644,"end":131959834,"strand":1,"description":"protein phosphatase 2 regulatory subunit Bdelta [Source:HGNC Symbol;Acc:HGNC:23732]"}, {"versioned_ensembl_gene_id":"ENSG00000205449.11","gene_symbol":"NBPF22P","gene_name":"NBPF member 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:28731]","synonyms":"MGC48637","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285622","summary":"This transcribed pseudogene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Jun 2013]","start":86282460,"end":86296463,"strand":1,"description":"NBPF member 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:28731]"}, {"versioned_ensembl_gene_id":"ENSG00000254066.1","gene_symbol":"LINC01938","gene_name":"long intergenic non-protein coding RNA 1938 [Source:HGNC Symbol;Acc:HGNC:52761]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377701","summary":null,"start":165220577,"end":165241752,"strand":-1,"description":"long intergenic non-protein coding RNA 1938 [Source:HGNC Symbol;Acc:HGNC:52761]"}, {"versioned_ensembl_gene_id":"ENSG00000130311.10","gene_symbol":"DDA1","gene_name":"DET1 and DDB1 associated 1 [Source:HGNC Symbol;Acc:HGNC:28360]","synonyms":"PCIA1,MGC2594,C19orf58","biotype":"protein_coding","ncbi_id":"79016","summary":null,"start":17309518,"end":17323301,"strand":1,"description":"DET1 and DDB1 associated 1 [Source:HGNC Symbol;Acc:HGNC:28360]"}, {"versioned_ensembl_gene_id":"ENSG00000280122.1","gene_symbol":"AC016168.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76966285,"end":76969530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267568.6","gene_symbol":"AC016168.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":76950317,"end":76969156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197483.9","gene_symbol":"ZNF628","gene_name":"zinc finger protein 628 [Source:HGNC Symbol;Acc:HGNC:28054]","synonyms":"Zfp628,ZEC","biotype":"protein_coding","ncbi_id":"89887","summary":"Zinc finger proteins (ZNFs), which bind nucleic acids, perform many key functions, the most important of which is regulating transcription. See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Mar 2008]","start":55476332,"end":55484487,"strand":1,"description":"zinc finger protein 628 [Source:HGNC Symbol;Acc:HGNC:28054]"}, {"versioned_ensembl_gene_id":"ENSG00000267521.1","gene_symbol":"AC016168.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76957023,"end":76958222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000022976.15","gene_symbol":"ZNF839","gene_name":"zinc finger protein 839 [Source:HGNC Symbol;Acc:HGNC:20345]","synonyms":"C14orf131","biotype":"protein_coding","ncbi_id":"55778","summary":null,"start":102317377,"end":102342702,"strand":1,"description":"zinc finger protein 839 [Source:HGNC Symbol;Acc:HGNC:20345]"}, {"versioned_ensembl_gene_id":"ENSG00000260111.1","gene_symbol":"AC012184.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70379457,"end":70399502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250327.1","gene_symbol":"RPSAP70","gene_name":"ribosomal protein SA pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:51923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105377595","summary":null,"start":186157896,"end":186158843,"strand":1,"description":"ribosomal protein SA pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:51923]"}, {"versioned_ensembl_gene_id":"ENSG00000196470.11","gene_symbol":"SIAH1","gene_name":"siah E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:10857]","synonyms":"hSIAH1","biotype":"protein_coding","ncbi_id":"6477","summary":"This gene encodes a protein that is a member of the seven in absentia homolog (SIAH) family. The protein is an E3 ligase and is involved in ubiquitination and proteasome-mediated degradation of specific proteins. The activity of this ubiquitin ligase has been implicated in the development of certain forms of Parkinson's disease, the regulation of the cellular response to hypoxia and induction of apoptosis. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized. [provided by RefSeq, Jul 2008]","start":48356364,"end":48448402,"strand":-1,"description":"siah E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:10857]"}, {"versioned_ensembl_gene_id":"ENSG00000230866.1","gene_symbol":"LINC02558","gene_name":"long intergenic non-protein coding RNA 2558 [Source:HGNC Symbol;Acc:HGNC:53597]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372999","summary":null,"start":31970823,"end":31973475,"strand":1,"description":"long intergenic non-protein coding RNA 2558 [Source:HGNC Symbol;Acc:HGNC:53597]"}, {"versioned_ensembl_gene_id":"ENSG00000277028.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724486,"end":54736500,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000254377.5","gene_symbol":"MIR124-2HG","gene_name":"MIR124-2 host gene [Source:HGNC Symbol;Acc:HGNC:48723]","synonyms":"LINC00966","biotype":"lincRNA","ncbi_id":"100130155","summary":null,"start":64373328,"end":64383787,"strand":1,"description":"MIR124-2 host gene [Source:HGNC Symbol;Acc:HGNC:48723]"}, {"versioned_ensembl_gene_id":"ENSG00000233236.1","gene_symbol":"AP001171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20256752,"end":20258820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229336.1","gene_symbol":"AP000568.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19739709,"end":19740150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213309.3","gene_symbol":"AL513043.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63615827,"end":63616361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250173.1","gene_symbol":"AC122719.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":979365,"end":981300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138071.13","gene_symbol":"ACTR2","gene_name":"ARP2 actin related protein 2 homolog [Source:HGNC Symbol;Acc:HGNC:169]","synonyms":"ARP2","biotype":"protein_coding","ncbi_id":"10097","summary":"The specific function of this gene has not yet been determined; however, the protein it encodes is known to be a major constituent of the ARP2/3 complex. This complex is located at the cell surface and is essential to cell shape and motility through lamellipodial actin assembly and protrusion. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":65227753,"end":65271253,"strand":1,"description":"ARP2 actin related protein 2 homolog [Source:HGNC Symbol;Acc:HGNC:169]"}, {"versioned_ensembl_gene_id":"ENSG00000226944.1","gene_symbol":"AL031847.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6204840,"end":6205780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248949.1","gene_symbol":"AC122719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":946315,"end":956520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236320.3","gene_symbol":"SLFN14","gene_name":"schlafen family member 14 [Source:HGNC Symbol;Acc:HGNC:32689]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342618","summary":"The protein encoded by this gene plays an important role in platelet formation and function. Defects in this gene are a cause of thrombocytopenia with excessive bleeding. [provided by RefSeq, Jul 2016]","start":35548125,"end":35558098,"strand":-1,"description":"schlafen family member 14 [Source:HGNC Symbol;Acc:HGNC:32689]"}, {"versioned_ensembl_gene_id":"ENSG00000227615.1","gene_symbol":"AP001324.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74745716,"end":74746114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224655.5","gene_symbol":"LINC01823","gene_name":"long intergenic non-protein coding RNA 1823 [Source:HGNC Symbol;Acc:HGNC:52628]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927801","summary":null,"start":121790444,"end":121796702,"strand":1,"description":"long intergenic non-protein coding RNA 1823 [Source:HGNC Symbol;Acc:HGNC:52628]"}, {"versioned_ensembl_gene_id":"ENSG00000272805.1","gene_symbol":"TAS2R10","gene_name":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]","synonyms":"T2R10,TRB2","biotype":"protein_coding","ncbi_id":"50839","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10825317,"end":10826358,"strand":-1,"description":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]"}, {"versioned_ensembl_gene_id":"ENSG00000261526.2","gene_symbol":"AC012615.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1874871,"end":1876169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267232.1","gene_symbol":"AC012615.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1875016,"end":1875992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154646.8","gene_symbol":"TMPRSS15","gene_name":"transmembrane protease, serine 15 [Source:HGNC Symbol;Acc:HGNC:9490]","synonyms":"PRSS7,MGC133046,ENTK","biotype":"protein_coding","ncbi_id":"5651","summary":"This gene encodes an enzyme that converts the pancreatic proenzyme trypsinogen to trypsin, which activates other proenzymes including chymotrypsinogen and procarboxypeptidases. The precursor protein is cleaved into two chains that form a heterodimer linked by a disulfide bond. This protein is a member of the trypsin family of peptidases. Mutations in this gene cause enterokinase deficiency, a malabsorption disorder characterized by diarrhea and failure to thrive. [provided by RefSeq, Jul 2008]","start":18269116,"end":18485879,"strand":-1,"description":"transmembrane protease, serine 15 [Source:HGNC Symbol;Acc:HGNC:9490]"}, {"versioned_ensembl_gene_id":"ENSG00000165805.9","gene_symbol":"C12orf50","gene_name":"chromosome 12 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:26665]","synonyms":"FLJ35821","biotype":"protein_coding","ncbi_id":"160419","summary":null,"start":87980035,"end":88034037,"strand":-1,"description":"chromosome 12 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:26665]"}, {"versioned_ensembl_gene_id":"ENSG00000267113.1","gene_symbol":"AF038458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35957121,"end":35957382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257256.1","gene_symbol":"AC008147.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50219604,"end":50229984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143401.14","gene_symbol":"ANP32E","gene_name":"acidic nuclear phosphoprotein 32 family member E [Source:HGNC Symbol;Acc:HGNC:16673]","synonyms":"MGC5350,LANPL,LANP-L","biotype":"protein_coding","ncbi_id":"81611","summary":null,"start":150218417,"end":150236156,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member E [Source:HGNC Symbol;Acc:HGNC:16673]"}, {"versioned_ensembl_gene_id":"ENSG00000124171.8","gene_symbol":"PARD6B","gene_name":"par-6 family cell polarity regulator beta [Source:HGNC Symbol;Acc:HGNC:16245]","synonyms":"PAR-6B","biotype":"protein_coding","ncbi_id":"84612","summary":"This gene is a member of the PAR6 family and encodes a protein with a PSD95/Discs-large/ZO1 (PDZ) domain, an OPR domain and a semi-Cdc42/Rac interactive binding (CRIB) domain. This cytoplasmic protein is involved in asymmetrical cell division and cell polarization processes as a member of a multi-protein complex. [provided by RefSeq, Jul 2008]","start":50731544,"end":50756795,"strand":1,"description":"par-6 family cell polarity regulator beta [Source:HGNC Symbol;Acc:HGNC:16245]"}, {"versioned_ensembl_gene_id":"ENSG00000253582.1","gene_symbol":"AC090579.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106520474,"end":106657548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162761.14","gene_symbol":"LMX1A","gene_name":"LIM homeobox transcription factor 1 alpha [Source:HGNC Symbol;Acc:HGNC:6653]","synonyms":"LMX1.1,LMX1","biotype":"protein_coding","ncbi_id":"4009","summary":"This gene encodes a homeodomain and LIM-domain containing protein. The encoded protein is a transcription factor that acts as a positive regulator of insulin gene transcription. This gene also plays a role in the development of dopamine producing neurons during embryogenesis. Mutations in this gene are associated with an increased risk of developing Parkinson's disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":165201867,"end":165356715,"strand":-1,"description":"LIM homeobox transcription factor 1 alpha [Source:HGNC Symbol;Acc:HGNC:6653]"}, {"versioned_ensembl_gene_id":"ENSG00000184207.8","gene_symbol":"PGP","gene_name":"phosphoglycolate phosphatase [Source:HGNC Symbol;Acc:HGNC:8909]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283871","summary":null,"start":2211997,"end":2214807,"strand":-1,"description":"phosphoglycolate phosphatase [Source:HGNC Symbol;Acc:HGNC:8909]"}, {"versioned_ensembl_gene_id":"ENSG00000259611.1","gene_symbol":"LINC01582","gene_name":"long intergenic non-protein coding RNA 1582 [Source:HGNC Symbol;Acc:HGNC:51416]","synonyms":"TCONS_00023827","biotype":"lincRNA","ncbi_id":"101927332","summary":null,"start":98085627,"end":98103712,"strand":-1,"description":"long intergenic non-protein coding RNA 1582 [Source:HGNC Symbol;Acc:HGNC:51416]"}, {"versioned_ensembl_gene_id":"ENSG00000011600.11","gene_symbol":"TYROBP","gene_name":"TYRO protein tyrosine kinase binding protein [Source:HGNC Symbol;Acc:HGNC:12449]","synonyms":"PLOSL,PLO-SL,KARAP,DAP12","biotype":"protein_coding","ncbi_id":"7305","summary":"This gene encodes a transmembrane signaling polypeptide which contains an immunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmic domain. The encoded protein may associate with the killer-cell inhibitory receptor (KIR) family of membrane glycoproteins and may act as an activating signal transduction element. This protein may bind zeta-chain (TCR) associated protein kinase 70kDa (ZAP-70) and spleen tyrosine kinase (SYK) and play a role in signal transduction, bone modeling, brain myelination, and inflammation. Mutations within this gene have been associated with polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease. Its putative receptor, triggering receptor expressed on myeloid cells 2 (TREM2), also causes PLOSL. Multiple alternative transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Mar 2010]","start":35904401,"end":35908295,"strand":-1,"description":"TYRO protein tyrosine kinase binding protein [Source:HGNC Symbol;Acc:HGNC:12449]"}, {"versioned_ensembl_gene_id":"ENSG00000216859.1","gene_symbol":"DHFRP5","gene_name":"dihydrofolate reductase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132056","summary":null,"start":62460940,"end":62461503,"strand":-1,"description":"dihydrofolate reductase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52355]"}, {"versioned_ensembl_gene_id":"ENSG00000217067.2","gene_symbol":"AL355375.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62547427,"end":62548272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265778.2","gene_symbol":"AC018413.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76491652,"end":76493918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235958.5","gene_symbol":"UBOX5-AS1","gene_name":"UBOX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44111]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100134015","summary":null,"start":3106913,"end":3150867,"strand":1,"description":"UBOX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44111]"}, {"versioned_ensembl_gene_id":"ENSG00000115137.11","gene_symbol":"DNAJC27","gene_name":"DnaJ heat shock protein family (Hsp40) member C27 [Source:HGNC Symbol;Acc:HGNC:30290]","synonyms":"RBJ,RabJS","biotype":"protein_coding","ncbi_id":"51277","summary":null,"start":24943636,"end":24972094,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C27 [Source:HGNC Symbol;Acc:HGNC:30290]"}, {"versioned_ensembl_gene_id":"ENSG00000237953.1","gene_symbol":"AC013267.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24968958,"end":24969224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113396.12","gene_symbol":"SLC27A6","gene_name":"solute carrier family 27 member 6 [Source:HGNC Symbol;Acc:HGNC:11000]","synonyms":"VLCS-H1,FATP6,FACVL2,ACSVL2","biotype":"protein_coding","ncbi_id":"28965","summary":"This gene encodes a member of the fatty acid transport protein family (FATP). FATPs are involved in the uptake of long-chain fatty acids and have unique expression patterns. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":128538013,"end":129033642,"strand":1,"description":"solute carrier family 27 member 6 [Source:HGNC Symbol;Acc:HGNC:11000]"}, {"versioned_ensembl_gene_id":"ENSG00000280062.1","gene_symbol":"AL031719.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1530715,"end":1533301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283123.1","gene_symbol":"RARRES2P11","gene_name":"retinoic acid receptor responder 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075248","summary":null,"start":29427400,"end":29427883,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51743]"}, {"versioned_ensembl_gene_id":"ENSG00000213003.3","gene_symbol":"BTF3P12","gene_name":"basic transcription factor 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:1127]","synonyms":"HUMBTFC,BTF3L2","biotype":"processed_pseudogene","ncbi_id":"652963","summary":"This locus represents a putative member of the BTF3 family of transcription factors. With no transcription yet documented, it is thought that this locus represents a pseudogene. [provided by RefSeq]","start":70273369,"end":70273837,"strand":1,"description":"basic transcription factor 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:1127]"}, {"versioned_ensembl_gene_id":"ENSG00000156049.6","gene_symbol":"GNA14","gene_name":"G protein subunit alpha 14 [Source:HGNC Symbol;Acc:HGNC:4382]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9630","summary":"This gene encodes a member of the guanine nucleotide-binding, or G protein family. G proteins are heterotrimers consisting of alpha, beta and gamma subunits. The encoded protein is a member of the alpha family of G proteins, more specifically the alpha q subfamily of G proteins. The encoded protein may play a role in pertussis-toxin resistant activation of phospholipase C-beta and its downstream effectors.[provided by RefSeq, Feb 2009]","start":77423079,"end":77648307,"strand":-1,"description":"G protein subunit alpha 14 [Source:HGNC Symbol;Acc:HGNC:4382]"}, {"versioned_ensembl_gene_id":"ENSG00000231373.1","gene_symbol":"GNA14-AS1","gene_name":"GNA14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50451]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927422","summary":null,"start":77456295,"end":77526697,"strand":1,"description":"GNA14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50451]"}, {"versioned_ensembl_gene_id":"ENSG00000172346.14","gene_symbol":"CSDC2","gene_name":"cold shock domain containing C2 [Source:HGNC Symbol;Acc:HGNC:30359]","synonyms":"PIPPin","biotype":"protein_coding","ncbi_id":"27254","summary":null,"start":41560763,"end":41577741,"strand":1,"description":"cold shock domain containing C2 [Source:HGNC Symbol;Acc:HGNC:30359]"}, {"versioned_ensembl_gene_id":"ENSG00000068650.18","gene_symbol":"ATP11A","gene_name":"ATPase phospholipid transporting 11A [Source:HGNC Symbol;Acc:HGNC:13552]","synonyms":"ATPIS,ATPIH,KIAA1021","biotype":"protein_coding","ncbi_id":"23250","summary":"The protein encoded by this gene is an integral membrane ATPase. The encoded protein is probably phosphorylated in its intermediate state and likely drives the transport of ions such as calcium across membranes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":112690329,"end":112887168,"strand":1,"description":"ATPase phospholipid transporting 11A [Source:HGNC Symbol;Acc:HGNC:13552]"}, {"versioned_ensembl_gene_id":"ENSG00000225914.1","gene_symbol":"AL671511.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32255711,"end":32265838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257855.1","gene_symbol":"AC126471.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85567878,"end":85568239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037042.8","gene_symbol":"TUBG2","gene_name":"tubulin gamma 2 [Source:HGNC Symbol;Acc:HGNC:12419]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27175","summary":null,"start":42659305,"end":42667006,"strand":1,"description":"tubulin gamma 2 [Source:HGNC Symbol;Acc:HGNC:12419]"}, {"versioned_ensembl_gene_id":"ENSG00000050426.15","gene_symbol":"LETMD1","gene_name":"LETM1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24241]","synonyms":"HCCR2,HCCR1,HCCR-2,HCCR-1,HCCR","biotype":"protein_coding","ncbi_id":"25875","summary":"This gene encodes a mitochondrial outer membrane protein. It has a potential role in tumorigenesis, which may result from negative regulation of the p53 tumor suppressor gene. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Aug 2011]","start":51047962,"end":51060424,"strand":1,"description":"LETM1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24241]"}, {"versioned_ensembl_gene_id":"ENSG00000185730.7","gene_symbol":"ZNF696","gene_name":"zinc finger protein 696 [Source:HGNC Symbol;Acc:HGNC:25872]","synonyms":"FLJ14129","biotype":"protein_coding","ncbi_id":"79943","summary":null,"start":143289676,"end":143298061,"strand":1,"description":"zinc finger protein 696 [Source:HGNC Symbol;Acc:HGNC:25872]"}, {"versioned_ensembl_gene_id":"ENSG00000250704.1","gene_symbol":"AC105343.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149956208,"end":149958572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267984.1","gene_symbol":"AC008750.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51345169,"end":51353293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233735.5","gene_symbol":"AL359918.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240177839,"end":240179644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234343.6","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31839844,"end":31845091,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000184990.12","gene_symbol":"SIVA1","gene_name":"SIVA1 apoptosis inducing factor [Source:HGNC Symbol;Acc:HGNC:17712]","synonyms":"Siva-2,Siva-1,SIVA,CD27BP","biotype":"protein_coding","ncbi_id":"10572","summary":"This gene encodes an E3 ubiquitin ligase that regulates cell cycle progression, cell proliferation and apoptosis. The N-terminus of this protein binds to the cytoplasmic tail of the CD27 antigen, a member of the tumor necrosis factor receptor (TNFR) superfamily. In response to UV radiation-induced DNA damage, this protein has been shown to mediate the ubiquitination of proliferating cell nuclear antigen (PCNA), an important step in translesion DNA synthesis. [provided by RefSeq, Sep 2018]","start":104753100,"end":104768494,"strand":1,"description":"SIVA1 apoptosis inducing factor [Source:HGNC Symbol;Acc:HGNC:17712]"}, {"versioned_ensembl_gene_id":"ENSG00000280287.1","gene_symbol":"AC131212.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132550729,"end":132554947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178947.8","gene_symbol":"SMIM10L2A","gene_name":"small integral membrane protein 10 like 2A [Source:HGNC Symbol;Acc:HGNC:34499]","synonyms":"NCRNA00086,MGC39606,LINC0086,LINC00086,LED","biotype":"protein_coding","ncbi_id":"399668","summary":"This gene encodes a highly conserved small protein that contains a conserved motif (DUF4560) and may function as an integral membrane protein. This transcript was also shown to associate with enhancer chromatin and therefore may also function as an RNA to regulate enhancers. [provided by RefSeq, Jan 2017]","start":135421943,"end":135428074,"strand":1,"description":"small integral membrane protein 10 like 2A [Source:HGNC Symbol;Acc:HGNC:34499]"}, {"versioned_ensembl_gene_id":"ENSG00000270510.1","gene_symbol":"AP000811.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87323709,"end":87324359,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182347.10","gene_symbol":"PDSS1P1","gene_name":"decaprenyl diphosphate synthase subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129248","summary":null,"start":5084999,"end":5086112,"strand":-1,"description":"decaprenyl diphosphate synthase subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49740]"}, {"versioned_ensembl_gene_id":"ENSG00000280150.1","gene_symbol":"AC148477.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132362810,"end":132363348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279946.1","gene_symbol":"AC244034.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":206541758,"end":206544892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234981.1","gene_symbol":"AC244034.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206528915,"end":206529706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229009.7","gene_symbol":"TMPRSS11GP","gene_name":"transmembrane protease, serine 11G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42983]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644759","summary":null,"start":67991684,"end":68015768,"strand":-1,"description":"transmembrane protease, serine 11G, pseudogene [Source:HGNC Symbol;Acc:HGNC:42983]"}, {"versioned_ensembl_gene_id":"ENSG00000248049.6","gene_symbol":"UBA6-AS1","gene_name":"UBA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49083]","synonyms":"LOC550112","biotype":"antisense_RNA","ncbi_id":"550112","summary":null,"start":67701280,"end":68080952,"strand":1,"description":"UBA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49083]"}, {"versioned_ensembl_gene_id":"ENSG00000270292.1","gene_symbol":"AC079880.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67725183,"end":67726395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249017.1","gene_symbol":"AC094108.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102500541,"end":102505670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074660.15","gene_symbol":"SCARF1","gene_name":"scavenger receptor class F member 1 [Source:HGNC Symbol;Acc:HGNC:16820]","synonyms":"SREC1,SREC,KIAA0149","biotype":"protein_coding","ncbi_id":"8578","summary":"The protein encoded by this gene is a scavenger receptor that is expressed in endothelial cells. It regulates the uptake of chemically modified low density lipoproteins, including acetylated low density lipoprotein (Ac-LDL), and it may be involved in atherogenesis. This gene is regulated by the transcription factors ZNF444/EZF-2 and SP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":1633858,"end":1645747,"strand":-1,"description":"scavenger receptor class F member 1 [Source:HGNC Symbol;Acc:HGNC:16820]"}, {"versioned_ensembl_gene_id":"ENSG00000267102.1","gene_symbol":"AC060766.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":35409602,"end":35410228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267648.1","gene_symbol":"AC060766.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":35406948,"end":35407818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267547.1","gene_symbol":"AC060766.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35403837,"end":35404373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240418.1","gene_symbol":"AC020917.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16412684,"end":16413576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267703.1","gene_symbol":"AC020917.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16440946,"end":16443584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182827.8","gene_symbol":"ACBD3","gene_name":"acyl-CoA binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15453]","synonyms":"PAP7,GOLPH1,GOCAP1,GCP60","biotype":"protein_coding","ncbi_id":"64746","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is involved in the maintenance of Golgi structure and function through its interaction with the integral membrane protein giantin. It may also be involved in the hormonal regulation of steroid formation. [provided by RefSeq, Jul 2008]","start":226144679,"end":226186730,"strand":-1,"description":"acyl-CoA binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15453]"}, {"versioned_ensembl_gene_id":"ENSG00000234478.1","gene_symbol":"ACBD3-AS1","gene_name":"ACBD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40701]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107985353","summary":null,"start":226148003,"end":226155071,"strand":1,"description":"ACBD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40701]"}, {"versioned_ensembl_gene_id":"ENSG00000138794.9","gene_symbol":"CASP6","gene_name":"caspase 6 [Source:HGNC Symbol;Acc:HGNC:1507]","synonyms":"MCH2","biotype":"protein_coding","ncbi_id":"839","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family of enzymes. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic acid residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein is processed by caspases 7, 8 and 10, and is thought to function as a downstream enzyme in the caspase activation cascade. Alternative splicing of this gene results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Oct 2015]","start":109688622,"end":109703583,"strand":-1,"description":"caspase 6 [Source:HGNC Symbol;Acc:HGNC:1507]"}, {"versioned_ensembl_gene_id":"ENSG00000162706.12","gene_symbol":"CADM3","gene_name":"cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:17601]","synonyms":"TSLL1,SynCAM3,NECL1,Necl-1,IGSF4B,FLJ10698,BIgR","biotype":"protein_coding","ncbi_id":"57863","summary":"The protein encoded by this gene is a calcium-independent cell-cell adhesion protein that can form homodimers or heterodimers with other nectin proteins. The encoded protein has both homophilic and heterophilic cell-cell adhesion activity. This gene is reported to be a tumor suppressor gene. [provided by RefSeq, Oct 2016]","start":159171609,"end":159203313,"strand":1,"description":"cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:17601]"}, {"versioned_ensembl_gene_id":"ENSG00000241105.1","gene_symbol":"AC022730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70506251,"end":70506818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230401.1","gene_symbol":"LINC01972","gene_name":"long intergenic non-protein coding RNA 1972 [Source:HGNC Symbol;Acc:HGNC:52798]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374293","summary":null,"start":194765238,"end":194768712,"strand":-1,"description":"long intergenic non-protein coding RNA 1972 [Source:HGNC Symbol;Acc:HGNC:52798]"}, {"versioned_ensembl_gene_id":"ENSG00000231978.2","gene_symbol":"AL590103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21768269,"end":21768575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146085.7","gene_symbol":"MUT","gene_name":"methylmalonyl-CoA mutase [Source:HGNC Symbol;Acc:HGNC:7526]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4594","summary":"This gene encodes the mitochondrial enzyme methylmalonyl Coenzyme A mutase. In humans, the product of this gene is a vitamin B12-dependent enzyme which catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA, while in other species this enzyme may have different functions. Mutations in this gene may lead to various types of methylmalonic aciduria. [provided by RefSeq, Jul 2008]","start":49430360,"end":49463191,"strand":-1,"description":"methylmalonyl-CoA mutase [Source:HGNC Symbol;Acc:HGNC:7526]"}, {"versioned_ensembl_gene_id":"ENSG00000176171.11","gene_symbol":"BNIP3","gene_name":"BCL2 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:1084]","synonyms":"Nip3","biotype":"protein_coding","ncbi_id":"664","summary":"This gene is encodes a mitochondrial protein that contains a BH3 domain and acts as a pro-apoptotic factor. The encoded protein interacts with anti-apoptotic proteins, including the E1B 19 kDa protein and Bcl2. This gene is silenced in tumors by DNA methylation. [provided by RefSeq, Dec 2014]","start":131966455,"end":131982013,"strand":-1,"description":"BCL2 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:1084]"}, {"versioned_ensembl_gene_id":"ENSG00000121769.7","gene_symbol":"FABP3","gene_name":"fatty acid binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3557]","synonyms":"O-FABP,MDGI,H-FABP,FABP11","biotype":"protein_coding","ncbi_id":"2170","summary":"The intracellular fatty acid-binding proteins (FABPs) belongs to a multigene family. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Fatty acid-binding protein 3 gene contains four exons and its function is to arrest growth of mammary epithelial cells. This gene is a candidate tumor suppressor gene for human breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":31365625,"end":31376850,"strand":-1,"description":"fatty acid binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3557]"}, {"versioned_ensembl_gene_id":"ENSG00000204363.4","gene_symbol":"SPANXN5","gene_name":"SPANX family member N5 [Source:HGNC Symbol;Acc:HGNC:33178]","synonyms":"SPANX-N5,CT11.10","biotype":"protein_coding","ncbi_id":"494197","summary":null,"start":52796144,"end":52798101,"strand":-1,"description":"SPANX family member N5 [Source:HGNC Symbol;Acc:HGNC:33178]"}, {"versioned_ensembl_gene_id":"ENSG00000270598.1","gene_symbol":"AL512343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226127178,"end":226127346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279781.1","gene_symbol":"AC079336.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32518322,"end":32518934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225518.2","gene_symbol":"LINC01703","gene_name":"long intergenic non-protein coding RNA 1703 [Source:HGNC Symbol;Acc:HGNC:52491]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373113","summary":null,"start":226083639,"end":226090292,"strand":1,"description":"long intergenic non-protein coding RNA 1703 [Source:HGNC Symbol;Acc:HGNC:52491]"}, {"versioned_ensembl_gene_id":"ENSG00000233268.3","gene_symbol":"AL691449.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9660828,"end":9662626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268652.1","gene_symbol":"AC063977.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51194118,"end":51195540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259556.2","gene_symbol":"AC090971.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51919073,"end":51930627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110237.3","gene_symbol":"ARHGEF17","gene_name":"Rho guanine nucleotide exchange factor 17 [Source:HGNC Symbol;Acc:HGNC:21726]","synonyms":"TEM4,p164-RhoGEF,KIAA0337","biotype":"protein_coding","ncbi_id":"9828","summary":null,"start":73308289,"end":73369091,"strand":1,"description":"Rho guanine nucleotide exchange factor 17 [Source:HGNC Symbol;Acc:HGNC:21726]"}, {"versioned_ensembl_gene_id":"ENSG00000224864.4","gene_symbol":"AC011447.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20125044,"end":20125484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267220.1","gene_symbol":"AC011447.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20131894,"end":20151908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106809.10","gene_symbol":"OGN","gene_name":"osteoglycin [Source:HGNC Symbol;Acc:HGNC:8126]","synonyms":"SLRR3A,OIF,mimecan","biotype":"protein_coding","ncbi_id":"4969","summary":"This gene encodes a member of the small leucine-rich proteoglycan (SLRP) family of proteins. The encoded protein induces ectopic bone formation in conjunction with transforming growth factor beta and may regulate osteoblast differentiation. High expression of the encoded protein may be associated with elevated heart left ventricular mass. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":92383967,"end":92404696,"strand":-1,"description":"osteoglycin [Source:HGNC Symbol;Acc:HGNC:8126]"}, {"versioned_ensembl_gene_id":"ENSG00000108187.15","gene_symbol":"PBLD","gene_name":"phenazine biosynthesis like protein domain containing [Source:HGNC Symbol;Acc:HGNC:23301]","synonyms":"MAWDBP,MAWBP,FLJ14767","biotype":"protein_coding","ncbi_id":"64081","summary":null,"start":68282660,"end":68333049,"strand":-1,"description":"phenazine biosynthesis like protein domain containing [Source:HGNC Symbol;Acc:HGNC:23301]"}, {"versioned_ensembl_gene_id":"ENSG00000198792.12","gene_symbol":"TMEM184B","gene_name":"transmembrane protein 184B [Source:HGNC Symbol;Acc:HGNC:1310]","synonyms":"HS5O6A,FM08,DKFZP586A1024,C22orf5","biotype":"protein_coding","ncbi_id":"25829","summary":null,"start":38219291,"end":38273034,"strand":-1,"description":"transmembrane protein 184B [Source:HGNC Symbol;Acc:HGNC:1310]"}, {"versioned_ensembl_gene_id":"ENSG00000196364.9","gene_symbol":"PRSS29P","gene_name":"protease, serine 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:17542]","synonyms":"Isp2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"123787","summary":null,"start":1260952,"end":1263845,"strand":-1,"description":"protease, serine 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:17542]"}, {"versioned_ensembl_gene_id":"ENSG00000235959.1","gene_symbol":"AC009237.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95640181,"end":95640604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231636.1","gene_symbol":"AGBL5-AS1","gene_name":"AGBL5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41133]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874031","summary":null,"start":27049683,"end":27050264,"strand":-1,"description":"AGBL5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41133]"}, {"versioned_ensembl_gene_id":"ENSG00000179981.9","gene_symbol":"TSHZ1","gene_name":"teashirt zinc finger homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10669]","synonyms":"TSH1,SDCCAG33,NY-CO-33","biotype":"protein_coding","ncbi_id":"10194","summary":"This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]","start":75210755,"end":75289950,"strand":1,"description":"teashirt zinc finger homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10669]"}, {"versioned_ensembl_gene_id":"ENSG00000242140.1","gene_symbol":"AC083904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181146233,"end":181146463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116254.17","gene_symbol":"CHD5","gene_name":"chromodomain helicase DNA binding protein 5 [Source:HGNC Symbol;Acc:HGNC:16816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26038","summary":"This gene encodes a member of the chromodomain helicase DNA-binding protein family. Members of this family are characterized by a chromodomain, a helicase ATP-binding domain and an additional functional domain. This gene encodes a neuron-specific protein that may function in chromatin remodeling and gene transcription. This gene is a potential tumor suppressor gene that may play a role in the development of neuroblastoma. [provided by RefSeq, Feb 2012]","start":6101793,"end":6180123,"strand":-1,"description":"chromodomain helicase DNA binding protein 5 [Source:HGNC Symbol;Acc:HGNC:16816]"}, {"versioned_ensembl_gene_id":"ENSG00000215105.4","gene_symbol":"TTC3P1","gene_name":"tetratricopeptide repeat domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23318]","synonyms":"TTC3L,RNF105L","biotype":"processed_pseudogene","ncbi_id":"286495","summary":null,"start":75740831,"end":75746911,"strand":-1,"description":"tetratricopeptide repeat domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23318]"}, {"versioned_ensembl_gene_id":"ENSG00000205133.11","gene_symbol":"TRIQK","gene_name":"triple QxxK/R motif containing [Source:HGNC Symbol;Acc:HGNC:27828]","synonyms":"PRO0845,LOC286144,DKFZp779L1068,C8orf83","biotype":"protein_coding","ncbi_id":"286144","summary":null,"start":92883530,"end":93017673,"strand":-1,"description":"triple QxxK/R motif containing [Source:HGNC Symbol;Acc:HGNC:27828]"}, {"versioned_ensembl_gene_id":"ENSG00000179241.12","gene_symbol":"LDLRAD3","gene_name":"low density lipoprotein receptor class A domain containing 3 [Source:HGNC Symbol;Acc:HGNC:27046]","synonyms":"LRAD3","biotype":"protein_coding","ncbi_id":"143458","summary":null,"start":35943981,"end":36232136,"strand":1,"description":"low density lipoprotein receptor class A domain containing 3 [Source:HGNC Symbol;Acc:HGNC:27046]"}, {"versioned_ensembl_gene_id":"ENSG00000119446.13","gene_symbol":"RBM18","gene_name":"RNA binding motif protein 18 [Source:HGNC Symbol;Acc:HGNC:28413]","synonyms":"MGC2734","biotype":"protein_coding","ncbi_id":"92400","summary":null,"start":122237624,"end":122264839,"strand":-1,"description":"RNA binding motif protein 18 [Source:HGNC Symbol;Acc:HGNC:28413]"}, {"versioned_ensembl_gene_id":"ENSG00000173930.8","gene_symbol":"SLCO4C1","gene_name":"solute carrier organic anion transporter family member 4C1 [Source:HGNC Symbol;Acc:HGNC:23612]","synonyms":"SLC21A20,OATPX,OATP4C1,OATP-H","biotype":"protein_coding","ncbi_id":"353189","summary":"SLCO4C1 belongs to the organic anion transporter (OATP) family. OATPs are involved in the membrane transport of bile acids, conjugated steroids, thyroid hormone, eicosanoids, peptides, and numerous drugs in many tissues (Mikkaichi et al., 2004 [PubMed 14993604]).[supplied by OMIM, Mar 2008]","start":102233986,"end":102296549,"strand":-1,"description":"solute carrier organic anion transporter family member 4C1 [Source:HGNC Symbol;Acc:HGNC:23612]"}, {"versioned_ensembl_gene_id":"ENSG00000179431.6","gene_symbol":"FJX1","gene_name":"four jointed box 1 [Source:HGNC Symbol;Acc:HGNC:17166]","synonyms":"FLJ25593,FLJ22416","biotype":"protein_coding","ncbi_id":"24147","summary":"The protein encoded by this gene is the human ortholog of mouse and Drosophila four-jointed gene product. The Drosophila protein is important for growth and differentiation of legs and wings, and for proper development of the eyes. The exact function of this gene in humans is not known. [provided by RefSeq, Jul 2008]","start":35618419,"end":35620868,"strand":1,"description":"four jointed box 1 [Source:HGNC Symbol;Acc:HGNC:17166]"}, {"versioned_ensembl_gene_id":"ENSG00000181449.3","gene_symbol":"SOX2","gene_name":"SRY-box 2 [Source:HGNC Symbol;Acc:HGNC:11195]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6657","summary":"This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008]","start":181711924,"end":181714436,"strand":1,"description":"SRY-box 2 [Source:HGNC Symbol;Acc:HGNC:11195]"}, {"versioned_ensembl_gene_id":"ENSG00000229719.5","gene_symbol":"MIR194-2HG","gene_name":"MIR194-2 host gene [Source:HGNC Symbol;Acc:HGNC:51946]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369343","summary":null,"start":64889560,"end":64893449,"strand":-1,"description":"MIR194-2 host gene [Source:HGNC Symbol;Acc:HGNC:51946]"}, {"versioned_ensembl_gene_id":"ENSG00000023318.7","gene_symbol":"ERP44","gene_name":"endoplasmic reticulum protein 44 [Source:HGNC Symbol;Acc:HGNC:18311]","synonyms":"TXNDC4,PDIA10,KIAA0573","biotype":"protein_coding","ncbi_id":"23071","summary":"This gene encodes a member of the protein disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins. It has an inferred N-terminal signal peptide, a catalytically active thioredoxin (TRX) domain, two TRX-like domains and a C-terminal ER-retention sequence. This protein functions as a pH-regulated chaperone of the secretory pathway and likely plays a role in protein quality control at the endoplasmic reticulum - Golgi interface. [provided by RefSeq, Dec 2016]","start":99979179,"end":100099040,"strand":-1,"description":"endoplasmic reticulum protein 44 [Source:HGNC Symbol;Acc:HGNC:18311]"}, {"versioned_ensembl_gene_id":"ENSG00000148187.17","gene_symbol":"MRRF","gene_name":"mitochondrial ribosome recycling factor [Source:HGNC Symbol;Acc:HGNC:7234]","synonyms":"RRF","biotype":"protein_coding","ncbi_id":"92399","summary":"This gene encodes a ribosome recycling factor, which is a component of the mitochondrial translational machinery. The encoded protein, along with mitochondrial elongation factor 2, functions in ribosomal recycling at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA. A pseudogene of this gene has been identified on chromosome X. [provided by RefSeq, Oct 2016]","start":122264603,"end":122331343,"strand":1,"description":"mitochondrial ribosome recycling factor [Source:HGNC Symbol;Acc:HGNC:7234]"}, {"versioned_ensembl_gene_id":"ENSG00000214435.7","gene_symbol":"AS3MT","gene_name":"arsenite methyltransferase [Source:HGNC Symbol;Acc:HGNC:17452]","synonyms":"CYT19","biotype":"protein_coding","ncbi_id":"57412","summary":"AS3MT catalyzes the transfer of a methyl group from S-adenosyl-L-methionine (AdoMet) to trivalent arsenical and may play a role in arsenic metabolism (Lin et al., 2002 [PubMed 11790780]).[supplied by OMIM, Mar 2008]","start":102869516,"end":102901899,"strand":1,"description":"arsenite methyltransferase [Source:HGNC Symbol;Acc:HGNC:17452]"}, {"versioned_ensembl_gene_id":"ENSG00000236937.2","gene_symbol":"PTGES3P4","gene_name":"prostaglandin E synthase 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43825]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480775","summary":null,"start":102845595,"end":102845950,"strand":1,"description":"prostaglandin E synthase 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43825]"}, {"versioned_ensembl_gene_id":"ENSG00000275046.1","gene_symbol":"AL603755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58386799,"end":58386961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235178.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994795,"end":29005326,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000278607.1","gene_symbol":"AC015819.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75070197,"end":75071091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234601.1","gene_symbol":"CHRM3-AS1","gene_name":"CHRM3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40150]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873984","summary":null,"start":239898016,"end":239899872,"strand":-1,"description":"CHRM3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40150]"}, {"versioned_ensembl_gene_id":"ENSG00000251332.1","gene_symbol":"AC021106.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37995494,"end":37996203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226445.1","gene_symbol":"BX322234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169213254,"end":169239565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268906.1","gene_symbol":"AC011473.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51030076,"end":51034335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283377.1","gene_symbol":"AL590396.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":237942698,"end":237943653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260083.1","gene_symbol":"MIR762HG","gene_name":"MIR762 host gene [Source:HGNC Symbol;Acc:HGNC:51386]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928736","summary":null,"start":30875222,"end":30895220,"strand":1,"description":"MIR762 host gene [Source:HGNC Symbol;Acc:HGNC:51386]"}, {"versioned_ensembl_gene_id":"ENSG00000126351.12","gene_symbol":"THRA","gene_name":"thyroid hormone receptor, alpha [Source:HGNC Symbol;Acc:HGNC:11796]","synonyms":"THRA3,THRA2,THRA1,NR1A1,ERBA1,ERBA,EAR-7.1/EAR-7.2,AR7","biotype":"protein_coding","ncbi_id":"7067","summary":"The protein encoded by this gene is a nuclear hormone receptor for triiodothyronine. It is one of the several receptors for thyroid hormone, and has been shown to mediate the biological activities of thyroid hormone. Knockout studies in mice suggest that the different receptors, while having certain extent of redundancy, may mediate different functions of thyroid hormone. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":40058290,"end":40093867,"strand":1,"description":"thyroid hormone receptor, alpha [Source:HGNC Symbol;Acc:HGNC:11796]"}, {"versioned_ensembl_gene_id":"ENSG00000236342.8","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"EST123147,ABC50","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30649829,"end":30675633,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000187790.10","gene_symbol":"FANCM","gene_name":"Fanconi anemia complementation group M [Source:HGNC Symbol;Acc:HGNC:23168]","synonyms":"KIAA1596,FAAP250","biotype":"protein_coding","ncbi_id":"57697","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":45135940,"end":45200890,"strand":1,"description":"Fanconi anemia complementation group M [Source:HGNC Symbol;Acc:HGNC:23168]"}, {"versioned_ensembl_gene_id":"ENSG00000254392.1","gene_symbol":"AC090539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50490795,"end":50491465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242294.6","gene_symbol":"STAG3L5P","gene_name":"stromal antigen 3-like 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:48896]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101735302","summary":null,"start":100336079,"end":100351900,"strand":1,"description":"stromal antigen 3-like 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:48896]"}, {"versioned_ensembl_gene_id":"ENSG00000260131.1","gene_symbol":"LINC00556","gene_name":"long intergenic non-protein coding RNA 556 [Source:HGNC Symbol;Acc:HGNC:43700]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861551","summary":null,"start":20181531,"end":20181942,"strand":1,"description":"long intergenic non-protein coding RNA 556 [Source:HGNC Symbol;Acc:HGNC:43700]"}, {"versioned_ensembl_gene_id":"ENSG00000230158.1","gene_symbol":"MTND1P28","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42077]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873215","summary":null,"start":117023918,"end":117024867,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42077]"}, {"versioned_ensembl_gene_id":"ENSG00000247570.2","gene_symbol":"SDCBPP2","gene_name":"syndecan binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129960","summary":null,"start":69942948,"end":69944648,"strand":1,"description":"syndecan binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44686]"}, {"versioned_ensembl_gene_id":"ENSG00000271667.1","gene_symbol":"AC104408.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116687218,"end":116687387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196098.2","gene_symbol":"OR5K4","gene_name":"olfactory receptor family 5 subfamily K member 4 [Source:HGNC Symbol;Acc:HGNC:31291]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403278","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98353854,"end":98354819,"strand":1,"description":"olfactory receptor family 5 subfamily K member 4 [Source:HGNC Symbol;Acc:HGNC:31291]"}, {"versioned_ensembl_gene_id":"ENSG00000235460.1","gene_symbol":"CR753651.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837878,"end":28839015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108518.7","gene_symbol":"PFN1","gene_name":"profilin 1 [Source:HGNC Symbol;Acc:HGNC:8881]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5216","summary":"This gene encodes a member of the profilin family of small actin-binding proteins. The encoded protein plays an important role in actin dynamics by regulating actin polymerization in response to extracellular signals. Deletion of this gene is associated with Miller-Dieker syndrome, and the encoded protein may also play a role in Huntington disease. Multiple pseudogenes of this gene are located on chromosome 1. [provided by RefSeq, Jul 2012]","start":4945652,"end":4949061,"strand":-1,"description":"profilin 1 [Source:HGNC Symbol;Acc:HGNC:8881]"}, {"versioned_ensembl_gene_id":"ENSG00000266865.6","gene_symbol":"AC138207.8","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31008497,"end":31093127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218730.1","gene_symbol":"AL117342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90116700,"end":90117105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122566.20","gene_symbol":"HNRNPA2B1","gene_name":"heterogeneous nuclear ribonucleoprotein A2/B1 [Source:HGNC Symbol;Acc:HGNC:5033]","synonyms":"HNRPA2B1","biotype":"protein_coding","ncbi_id":"3181","summary":"This gene belongs to the A/B subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two repeats of quasi-RRM domains that bind to RNAs. This gene has been described to generate two alternatively spliced transcript variants which encode different isoforms. [provided by RefSeq, Jul 2008]","start":26189927,"end":26201529,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A2/B1 [Source:HGNC Symbol;Acc:HGNC:5033]"}, {"versioned_ensembl_gene_id":"ENSG00000231322.5","gene_symbol":"RPL13AP17","gene_name":"ribosomal protein L13a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36167]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"399670","summary":null,"start":78347142,"end":78359458,"strand":1,"description":"ribosomal protein L13a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36167]"}, {"versioned_ensembl_gene_id":"ENSG00000222024.2","gene_symbol":"AC004945.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79353410,"end":79354392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280958.1","gene_symbol":"AC004808.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78170195,"end":78170915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271919.1","gene_symbol":"AC005828.7","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":63331984,"end":63332539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226797.1","gene_symbol":"AC005828.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63381231,"end":63414312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225122.1","gene_symbol":"AL603841.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":163422405,"end":163423164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260507.1","gene_symbol":"AC133919.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90105095,"end":90106316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230820.2","gene_symbol":"AC000362.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126980967,"end":126981778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279133.1","gene_symbol":"AC018628.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":62003700,"end":62007518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137177.19","gene_symbol":"KIF13A","gene_name":"kinesin family member 13A [Source:HGNC Symbol;Acc:HGNC:14566]","synonyms":"bA500C11.2","biotype":"protein_coding","ncbi_id":"63971","summary":"This gene encodes a member of the kinesin family of microtubule-based motor proteins that function in the positioning of endosomes. This family member can direct mannose-6-phosphate receptor-containing vesicles from the trans-Golgi network to the plasma membrane, and it is necessary for the steady-state distribution of late endosomes/lysosomes. It is also required for the translocation of FYVE-CENT and TTC19 from the centrosome to the midbody during cytokinesis, and it plays a role in melanosome maturation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":17759183,"end":17987623,"strand":-1,"description":"kinesin family member 13A [Source:HGNC Symbol;Acc:HGNC:14566]"}, {"versioned_ensembl_gene_id":"ENSG00000244585.1","gene_symbol":"RPL12P33","gene_name":"ribosomal protein L12 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643550","summary":null,"start":120916745,"end":120917236,"strand":1,"description":"ribosomal protein L12 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35696]"}, {"versioned_ensembl_gene_id":"ENSG00000227120.1","gene_symbol":"AC009238.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95436133,"end":95436556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118412.12","gene_symbol":"CASP8AP2","gene_name":"caspase 8 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:1510]","synonyms":"RIP25,KIAA1315,FLJ11208,FLASH,CED-4","biotype":"protein_coding","ncbi_id":"9994","summary":"This protein is highly similar to FLASH, a mouse apoptotic protein identified by its interaction with the death-effector domain (DED) of caspase 8. Studies of FLASH protein suggested that this protein may be a component of the death-inducing signaling complex that includes Fas receptor, Fas-binding adapter FADD, and caspase 8, and plays a regulatory role in Fas-mediated apoptosis. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Nov 2008]","start":89829894,"end":89874436,"strand":1,"description":"caspase 8 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:1510]"}, {"versioned_ensembl_gene_id":"ENSG00000220548.3","gene_symbol":"VIM2P","gene_name":"vimentin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:43891]","synonyms":"VIMP1,VIM2,RP11-162L10.1,lncRNA-CIR","biotype":"processed_pseudogene","ncbi_id":"100130535","summary":null,"start":126602356,"end":126603649,"strand":-1,"description":"vimentin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:43891]"}, {"versioned_ensembl_gene_id":"ENSG00000100647.7","gene_symbol":"SUSD6","gene_name":"sushi domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19956]","synonyms":"KIAA0247","biotype":"protein_coding","ncbi_id":"9766","summary":null,"start":69611596,"end":69715142,"strand":1,"description":"sushi domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19956]"}, {"versioned_ensembl_gene_id":"ENSG00000253420.1","gene_symbol":"AC103853.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105662352,"end":105685765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176022.4","gene_symbol":"B3GALT6","gene_name":"beta-1,3-galactosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:17978]","synonyms":"beta3GalT6","biotype":"protein_coding","ncbi_id":"126792","summary":"The enzyme encoded by this intronless gene is a beta-1,3-galactosyltransferase found in the medial Golgi apparatus, where it catalyzes the transfer of galactose from UDP-galactose to substrates containing a terminal beta-linked galactose moiety. The encoded enzyme has a particular affinity for galactose-beta-1,4-xylose found in the linker region of glycosamines. This enzyme is required for glycosaminoglycan synthesis. [provided by RefSeq, Jun 2013]","start":1232265,"end":1235041,"strand":1,"description":"beta-1,3-galactosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:17978]"}, {"versioned_ensembl_gene_id":"ENSG00000144749.13","gene_symbol":"LRIG1","gene_name":"leucine rich repeats and immunoglobulin like domains 1 [Source:HGNC Symbol;Acc:HGNC:17360]","synonyms":"LIG-1,DKFZP586O1624,LIG1","biotype":"protein_coding","ncbi_id":"26018","summary":null,"start":66378797,"end":66501263,"strand":-1,"description":"leucine rich repeats and immunoglobulin like domains 1 [Source:HGNC Symbol;Acc:HGNC:17360]"}, {"versioned_ensembl_gene_id":"ENSG00000253318.1","gene_symbol":"TMCC1P1","gene_name":"transmembrane and coiled-coil domain family 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31901]","synonyms":"TMCC1P","biotype":"processed_pseudogene","ncbi_id":"100128132","summary":null,"start":105194990,"end":105196969,"strand":-1,"description":"transmembrane and coiled-coil domain family 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31901]"}, {"versioned_ensembl_gene_id":"ENSG00000251003.7","gene_symbol":"ZFPM2-AS1","gene_name":"ZFPM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50698]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"102723356","summary":null,"start":105780246,"end":106060524,"strand":-1,"description":"ZFPM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50698]"}, {"versioned_ensembl_gene_id":"ENSG00000240433.4","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31709833,"end":31713000,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000115363.13","gene_symbol":"EVA1A","gene_name":"eva-1 homolog A, regulator of programmed cell death [Source:HGNC Symbol;Acc:HGNC:25816]","synonyms":"TMEM166,FLJ13391,FAM176A","biotype":"protein_coding","ncbi_id":"84141","summary":null,"start":75469302,"end":75569722,"strand":-1,"description":"eva-1 homolog A, regulator of programmed cell death [Source:HGNC Symbol;Acc:HGNC:25816]"}, {"versioned_ensembl_gene_id":"ENSG00000248928.1","gene_symbol":"AC008837.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99594880,"end":99595297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231793.5","gene_symbol":"DOC2GP","gene_name":"double C2 domain gamma pseudogene [Source:HGNC Symbol;Acc:HGNC:37962]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"390213","summary":null,"start":67612651,"end":67616257,"strand":-1,"description":"double C2 domain gamma pseudogene [Source:HGNC Symbol;Acc:HGNC:37962]"}, {"versioned_ensembl_gene_id":"ENSG00000255349.1","gene_symbol":"OR4A7P","gene_name":"olfactory receptor family 4 subfamily A member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15164]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81316","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54692450,"end":54693359,"strand":1,"description":"olfactory receptor family 4 subfamily A member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15164]"}, {"versioned_ensembl_gene_id":"ENSG00000274652.1","gene_symbol":"AL157817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51180178,"end":51180967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253630.1","gene_symbol":"AC026407.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157747504,"end":157747707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231897.1","gene_symbol":"MARK2P14","gene_name":"microtubule affinity regulating kinase 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44495]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631261","summary":null,"start":11906527,"end":11912313,"strand":1,"description":"microtubule affinity regulating kinase 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44495]"}, {"versioned_ensembl_gene_id":"ENSG00000261232.2","gene_symbol":"AC090751.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76472099,"end":76472365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135605.12","gene_symbol":"TEC","gene_name":"tec protein tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11719]","synonyms":"PSCTK4","biotype":"protein_coding","ncbi_id":"7006","summary":"The protein encoded by this gene belongs to the Tec family of non-receptor protein-tyrosine kinases containing a pleckstrin homology domain. Tec family kinases are involved in the intracellular signaling mechanisms of cytokine receptors, lymphocyte surface antigens, heterotrimeric G-protein coupled receptors, and integrin molecules. They are also key players in the regulation of the immune functions. Tec kinase is an integral component of T cell signaling and has a distinct role in T cell activation. This gene may be associated with myelodysplastic syndrome. [provided by RefSeq, Jul 2008]","start":48135783,"end":48269864,"strand":-1,"description":"tec protein tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11719]"}, {"versioned_ensembl_gene_id":"ENSG00000270188.1","gene_symbol":"MTRNR2L11","gene_name":"MT-RNR2-like 11 [Source:HGNC Symbol;Acc:HGNC:37168]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463489","summary":null,"start":237943724,"end":237945275,"strand":-1,"description":"MT-RNR2-like 11 [Source:HGNC Symbol;Acc:HGNC:37168]"}, {"versioned_ensembl_gene_id":"ENSG00000164051.13","gene_symbol":"CCDC51","gene_name":"coiled-coil domain containing 51 [Source:HGNC Symbol;Acc:HGNC:25714]","synonyms":"FLJ12436","biotype":"protein_coding","ncbi_id":"79714","summary":null,"start":48432164,"end":48440456,"strand":-1,"description":"coiled-coil domain containing 51 [Source:HGNC Symbol;Acc:HGNC:25714]"}, {"versioned_ensembl_gene_id":"ENSG00000278813.1","gene_symbol":"AC006133.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39726030,"end":39726775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251381.7","gene_symbol":"LINC00958","gene_name":"long intergenic non-protein coding RNA 958 [Source:HGNC Symbol;Acc:HGNC:48671]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506305","summary":null,"start":12961842,"end":12989548,"strand":-1,"description":"long intergenic non-protein coding RNA 958 [Source:HGNC Symbol;Acc:HGNC:48671]"}, {"versioned_ensembl_gene_id":"ENSG00000248365.3","gene_symbol":"POU5F1P7","gene_name":"POU class 5 homeobox 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33313]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100009669","summary":null,"start":98119191,"end":98119731,"strand":1,"description":"POU class 5 homeobox 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33313]"}, {"versioned_ensembl_gene_id":"ENSG00000135312.6","gene_symbol":"HTR1B","gene_name":"5-hydroxytryptamine receptor 1B [Source:HGNC Symbol;Acc:HGNC:5287]","synonyms":"HTR1D2,5-HT1DB,5-HT1B,S12","biotype":"protein_coding","ncbi_id":"3351","summary":"The protein encoded by this intronless gene is a G-protein coupled receptor for serotonin (5-hydroxytryptamine). Ligand binding activates second messengers that inhibit the activity of adenylate cyclase and manage the release of serotonin, dopamine, and acetylcholine in the brain. The encoded protein may be involved in several neuropsychiatric disorders and therefore is often a target of antidepressant and other psychotherapeutic drugs. [provided by RefSeq, Nov 2015]","start":77461753,"end":77463773,"strand":-1,"description":"5-hydroxytryptamine receptor 1B [Source:HGNC Symbol;Acc:HGNC:5287]"}, {"versioned_ensembl_gene_id":"ENSG00000231842.1","gene_symbol":"AC020559.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126177193,"end":126202239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253798.2","gene_symbol":"AC008694.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157682985,"end":157690878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213439.3","gene_symbol":"OR5AC1","gene_name":"olfactory receptor family 5 subfamily AC member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15047]","synonyms":"OR5AC1P","biotype":"polymorphic_pseudogene","ncbi_id":"81431","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":98064472,"end":98065396,"strand":1,"description":"olfactory receptor family 5 subfamily AC member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15047]"}, {"versioned_ensembl_gene_id":"ENSG00000117724.12","gene_symbol":"CENPF","gene_name":"centromere protein F [Source:HGNC Symbol;Acc:HGNC:1857]","synonyms":"hcp-1","biotype":"protein_coding","ncbi_id":"1063","summary":"This gene encodes a protein that associates with the centromere-kinetochore complex. The protein is a component of the nuclear matrix during the G2 phase of interphase. In late G2 the protein associates with the kinetochore and maintains this association through early anaphase. It localizes to the spindle midzone and the intracellular bridge in late anaphase and telophase, respectively, and is thought to be subsequently degraded. The localization of this protein suggests that it may play a role in chromosome segregation during mitotis. It is thought to form either a homodimer or heterodimer. Autoantibodies against this protein have been found in patients with cancer or graft versus host disease. [provided by RefSeq, Jul 2008]","start":214603195,"end":214664588,"strand":1,"description":"centromere protein F [Source:HGNC Symbol;Acc:HGNC:1857]"}, {"versioned_ensembl_gene_id":"ENSG00000213753.10","gene_symbol":"CENPBD1P1","gene_name":"CENPB DNA-binding domains containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28421]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"65996","summary":null,"start":58573503,"end":58599801,"strand":1,"description":"CENPB DNA-binding domains containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28421]"}, {"versioned_ensembl_gene_id":"ENSG00000166183.15","gene_symbol":"ASPG","gene_name":"asparaginase [Source:HGNC Symbol;Acc:HGNC:20123]","synonyms":"C14orf76","biotype":"protein_coding","ncbi_id":"374569","summary":null,"start":104085679,"end":104115581,"strand":1,"description":"asparaginase [Source:HGNC Symbol;Acc:HGNC:20123]"}, {"versioned_ensembl_gene_id":"ENSG00000276466.1","gene_symbol":"AC008984.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54328223,"end":54329236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244019.1","gene_symbol":"AC010234.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77545397,"end":77546266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116996.9","gene_symbol":"ZP4","gene_name":"zona pellucida glycoprotein 4 [Source:HGNC Symbol;Acc:HGNC:15770]","synonyms":"ZPB","biotype":"protein_coding","ncbi_id":"57829","summary":"The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed primarily of three or four glycoproteins with various functions during fertilization and preimplantation development. The nascent protein contains a N-terminal signal peptide sequence, a conserved ZP domain, a consensus furin cleavage site, and a C-terminal transmembrane domain. It is hypothesized that furin cleavage results in release of the mature protein from the plasma membrane for subsequent incorporation into the zona pellucida matrix. However, the requirement for furin cleavage in this process remains controversial based on mouse studies. Previously, this gene has been referred to as ZP1 or ZPB and thought to have similar functions as mouse Zp1. However, a human gene with higher similarity and chromosomal synteny to mouse Zp1 has been assigned the symbol ZP1 and this gene has been assigned the symbol ZP4. [provided by RefSeq, Jul 2008]","start":237877864,"end":237890922,"strand":-1,"description":"zona pellucida glycoprotein 4 [Source:HGNC Symbol;Acc:HGNC:15770]"}, {"versioned_ensembl_gene_id":"ENSG00000127837.9","gene_symbol":"AAMP","gene_name":"angio associated migratory cell protein [Source:HGNC Symbol;Acc:HGNC:18]","synonyms":null,"biotype":"protein_coding","ncbi_id":"14","summary":"The gene is a member of the immunoglobulin superfamily. The encoded protein is associated with angiogenesis, with potential roles in endothelial tube formation and the migration of endothelial cells. It may also regulate smooth muscle cell migration via the RhoA pathway. The encoded protein can bind to heparin and may mediate heparin-sensitive cell adhesion. [provided by RefSeq, Oct 2014]","start":218264123,"end":218270257,"strand":-1,"description":"angio associated migratory cell protein [Source:HGNC Symbol;Acc:HGNC:18]"}, {"versioned_ensembl_gene_id":"ENSG00000248821.1","gene_symbol":"AC009238.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95413456,"end":95414296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258559.2","gene_symbol":"AC005519.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":74289127,"end":74294425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146457.14","gene_symbol":"WTAP","gene_name":"WT1 associated protein [Source:HGNC Symbol;Acc:HGNC:16846]","synonyms":"Mum2,MGC3925,KIAA0105","biotype":"protein_coding","ncbi_id":"9589","summary":"The Wilms tumor suppressor gene WT1 appears to play a role in both transcriptional and posttranscriptional regulation of certain cellular genes. This gene encodes a WT1-associating protein, which is a ubiquitously expressed nuclear protein. Like WT1 protein, this protein is localized throughout the nucleoplasm as well as in speckles and partially colocalizes with splicing factors. Alternative splicing of this gene results in several transcript variants encoding three different isoforms. [provided by RefSeq, Jul 2012]","start":159725585,"end":159756319,"strand":1,"description":"WT1 associated protein [Source:HGNC Symbol;Acc:HGNC:16846]"}, {"versioned_ensembl_gene_id":"ENSG00000234519.1","gene_symbol":"AL109924.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169067818,"end":169069424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197826.11","gene_symbol":"C4orf22","gene_name":"chromosome 4 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:28554]","synonyms":null,"biotype":"protein_coding","ncbi_id":"255119","summary":null,"start":80335720,"end":80963756,"strand":1,"description":"chromosome 4 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:28554]"}, {"versioned_ensembl_gene_id":"ENSG00000254824.1","gene_symbol":"AP003461.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103409580,"end":103409657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235815.1","gene_symbol":"AL136099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168716606,"end":168723495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259093.1","gene_symbol":"AL137191.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63123033,"end":63128214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105198.10","gene_symbol":"LGALS13","gene_name":"galectin 13 [Source:HGNC Symbol;Acc:HGNC:15449]","synonyms":"PP13,PLAC8","biotype":"protein_coding","ncbi_id":"29124","summary":"Lysophospholipases are enzymes that act on biological membranes to regulate the multifunctional lysophospholipids. The protein encoded by this gene has lysophospholipase activity. It is composed of two identical subunits which are held together by disulfide bonds. This protein has structural similarity to several members of the beta-galactoside-binding S-type lectin family. [provided by RefSeq, Jul 2008]","start":39602501,"end":39607476,"strand":1,"description":"galectin 13 [Source:HGNC Symbol;Acc:HGNC:15449]"}, {"versioned_ensembl_gene_id":"ENSG00000215819.3","gene_symbol":"KRT18P12","gene_name":"keratin 18 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:33410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643471","summary":null,"start":214532195,"end":214533467,"strand":1,"description":"keratin 18 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:33410]"}, {"versioned_ensembl_gene_id":"ENSG00000228470.1","gene_symbol":"AL929236.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":214344172,"end":214357615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251391.4","gene_symbol":"AC113378.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66298468,"end":66322944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244593.1","gene_symbol":"AC025062.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18383274,"end":18383917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225194.2","gene_symbol":"LINC00092","gene_name":"long intergenic non-protein coding RNA 92 [Source:HGNC Symbol;Acc:HGNC:31408]","synonyms":"NCRNA00092,bA346B7.1","biotype":"lincRNA","ncbi_id":"100188953","summary":null,"start":96019732,"end":96027965,"strand":-1,"description":"long intergenic non-protein coding RNA 92 [Source:HGNC Symbol;Acc:HGNC:31408]"}, {"versioned_ensembl_gene_id":"ENSG00000275246.2","gene_symbol":"TLCD2","gene_name":"TLC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"727910","summary":null,"start":1702790,"end":1710438,"strand":-1,"description":"TLC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33522]"}, {"versioned_ensembl_gene_id":"ENSG00000282137.1","gene_symbol":"OR4G3P","gene_name":"olfactory receptor family 4 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8304]","synonyms":"OR4G5P,OR4G3,OLC-7501,OLC","biotype":"unprocessed_pseudogene","ncbi_id":"26679","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":94062,"end":94974,"strand":1,"description":"olfactory receptor family 4 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8304]"}, {"versioned_ensembl_gene_id":"ENSG00000236785.1","gene_symbol":"SDR42E1P5","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51832]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422339","summary":null,"start":102411243,"end":102412108,"strand":1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51832]"}, {"versioned_ensembl_gene_id":"ENSG00000178715.8","gene_symbol":"AL450998.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15828232,"end":15828669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112096.16","gene_symbol":"SOD2","gene_name":"superoxide dismutase 2 [Source:HGNC Symbol;Acc:HGNC:11180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6648","summary":"This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. [provided by RefSeq, Apr 2016]","start":159669057,"end":159762529,"strand":-1,"description":"superoxide dismutase 2 [Source:HGNC Symbol;Acc:HGNC:11180]"}, {"versioned_ensembl_gene_id":"ENSG00000273579.3","gene_symbol":"C22orf15","gene_name":"chromosome 22 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:15558]","synonyms":"N27C7-3,FLJ36561","biotype":"protein_coding","ncbi_id":"150248","summary":null,"start":23764087,"end":23765861,"strand":1,"description":"chromosome 22 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:15558]"}, {"versioned_ensembl_gene_id":"ENSG00000175773.12","gene_symbol":"AP002986.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130314993,"end":130403657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255358.1","gene_symbol":"AC019227.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130285023,"end":130285833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255220.1","gene_symbol":"DDX18P5","gene_name":"DEAD-box helicase 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646378","summary":null,"start":130295641,"end":130296946,"strand":1,"description":"DEAD-box helicase 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33968]"}, {"versioned_ensembl_gene_id":"ENSG00000255207.1","gene_symbol":"AL133399.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33450646,"end":33450943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243581.1","gene_symbol":"RPS29P25","gene_name":"ribosomal protein S29 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271590","summary":null,"start":39590981,"end":39591151,"strand":1,"description":"ribosomal protein S29 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35649]"}, {"versioned_ensembl_gene_id":"ENSG00000197734.8","gene_symbol":"C14orf178","gene_name":"chromosome 14 open reading frame 178 [Source:HGNC Symbol;Acc:HGNC:26385]","synonyms":"FLJ25976","biotype":"protein_coding","ncbi_id":"283579","summary":null,"start":77760830,"end":77769742,"strand":1,"description":"chromosome 14 open reading frame 178 [Source:HGNC Symbol;Acc:HGNC:26385]"}, {"versioned_ensembl_gene_id":"ENSG00000226193.1","gene_symbol":"AL049548.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152402398,"end":152404966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255199.2","gene_symbol":"GTF2IP11","gene_name":"general transcription factor IIi pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51724]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480346","summary":null,"start":50100892,"end":50102898,"strand":-1,"description":"general transcription factor IIi pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51724]"}, {"versioned_ensembl_gene_id":"ENSG00000160932.10","gene_symbol":"LY6E","gene_name":"lymphocyte antigen 6 family member E [Source:HGNC Symbol;Acc:HGNC:6727]","synonyms":"RIG-E,TSA-1,SCA-2","biotype":"protein_coding","ncbi_id":"4061","summary":null,"start":143017982,"end":143023832,"strand":1,"description":"lymphocyte antigen 6 family member E [Source:HGNC Symbol;Acc:HGNC:6727]"}, {"versioned_ensembl_gene_id":"ENSG00000228170.1","gene_symbol":"AL031963.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3138394,"end":3153062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188185.11","gene_symbol":"LINC00265","gene_name":"long intergenic non-protein coding RNA 265 [Source:HGNC Symbol;Acc:HGNC:28019]","synonyms":"NCRNA00265-1,NCRNA00265","biotype":"lincRNA","ncbi_id":"349114","summary":null,"start":39733632,"end":39793092,"strand":1,"description":"long intergenic non-protein coding RNA 265 [Source:HGNC Symbol;Acc:HGNC:28019]"}, {"versioned_ensembl_gene_id":"ENSG00000227729.3","gene_symbol":"RD3L","gene_name":"retinal degeneration 3-like [Source:HGNC Symbol;Acc:HGNC:40912]","synonyms":"TDRD9AS1,TDRD9-AS1","biotype":"protein_coding","ncbi_id":"647286","summary":null,"start":103940426,"end":103942308,"strand":-1,"description":"retinal degeneration 3-like [Source:HGNC Symbol;Acc:HGNC:40912]"}, {"versioned_ensembl_gene_id":"ENSG00000165283.15","gene_symbol":"STOML2","gene_name":"stomatin like 2 [Source:HGNC Symbol;Acc:HGNC:14559]","synonyms":"SLP-2,HSPC108","biotype":"protein_coding","ncbi_id":"30968","summary":null,"start":35099776,"end":35103195,"strand":-1,"description":"stomatin like 2 [Source:HGNC Symbol;Acc:HGNC:14559]"}, {"versioned_ensembl_gene_id":"ENSG00000251048.1","gene_symbol":"AC093871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18488062,"end":18489508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251144.1","gene_symbol":"AC113346.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174820027,"end":174826324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278790.1","gene_symbol":"DUX4L12","gene_name":"double homeobox 4 like 12 [Source:HGNC Symbol;Acc:HGNC:38671]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440014","summary":null,"start":133749950,"end":133751216,"strand":1,"description":"double homeobox 4 like 12 [Source:HGNC Symbol;Acc:HGNC:38671]"}, {"versioned_ensembl_gene_id":"ENSG00000237635.2","gene_symbol":"DUX4L29","gene_name":"double homeobox 4 like 29 [Source:HGNC Symbol;Acc:HGNC:51606]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481970","summary":null,"start":133740606,"end":133741284,"strand":1,"description":"double homeobox 4 like 29 [Source:HGNC Symbol;Acc:HGNC:51606]"}, {"versioned_ensembl_gene_id":"ENSG00000276964.1","gene_symbol":"DUX4L23","gene_name":"double homeobox 4 like 23 [Source:HGNC Symbol;Acc:HGNC:50804]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723472","summary":null,"start":133673749,"end":133675017,"strand":1,"description":"double homeobox 4 like 23 [Source:HGNC Symbol;Acc:HGNC:50804]"}, {"versioned_ensembl_gene_id":"ENSG00000263766.5","gene_symbol":"AC025682.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47603860,"end":47649420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154839.9","gene_symbol":"SKA1","gene_name":"spindle and kinetochore associated complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28109]","synonyms":"MGC10200,C18orf24","biotype":"protein_coding","ncbi_id":"220134","summary":null,"start":50374995,"end":50394173,"strand":1,"description":"spindle and kinetochore associated complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28109]"}, {"versioned_ensembl_gene_id":"ENSG00000233020.1","gene_symbol":"AL354872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70530526,"end":70531492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279277.1","gene_symbol":"AC012020.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108036718,"end":108038445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254472.1","gene_symbol":"OR4A49P","gene_name":"olfactory receptor family 4 subfamily A member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31268]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403255","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49915013,"end":49915644,"strand":-1,"description":"olfactory receptor family 4 subfamily A member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31268]"}, {"versioned_ensembl_gene_id":"ENSG00000279423.1","gene_symbol":"AL445363.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34541044,"end":34541714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279626.1","gene_symbol":"DUX4L28","gene_name":"double homeobox 4 like 28 [Source:HGNC Symbol;Acc:HGNC:51605]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481728","summary":null,"start":133664429,"end":133665106,"strand":1,"description":"double homeobox 4 like 28 [Source:HGNC Symbol;Acc:HGNC:51605]"}, {"versioned_ensembl_gene_id":"ENSG00000279059.1","gene_symbol":"AC007485.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":54956760,"end":54958426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134470.20","gene_symbol":"IL15RA","gene_name":"interleukin 15 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5978]","synonyms":"IL-15RA,CD215","biotype":"protein_coding","ncbi_id":"3601","summary":"This gene encodes a cytokine receptor that specifically binds interleukin 15 (IL15) with high affinity. The receptors of IL15 and IL2 share two subunits, IL2R beta and IL2R gamma. This forms the basis of many overlapping biological activities of IL15 and IL2. The protein encoded by this gene is structurally related to IL2R alpha, an additional IL2-specific alpha subunit necessary for high affinity IL2 binding. Unlike IL2RA, IL15RA is capable of binding IL15 with high affinity independent of other subunits, which suggests distinct roles between IL15 and IL2. This receptor is reported to enhance cell proliferation and expression of apoptosis inhibitor BCL2L1/BCL2-XL and BCL2. Multiple alternatively spliced transcript variants of this gene have been reported.[provided by RefSeq, Apr 2010]","start":5943639,"end":5978187,"strand":-1,"description":"interleukin 15 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5978]"}, {"versioned_ensembl_gene_id":"ENSG00000083520.14","gene_symbol":"DIS3","gene_name":"DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease [Source:HGNC Symbol;Acc:HGNC:20604]","synonyms":"RRP44,KIAA1008,EXOSC11,dis3p","biotype":"protein_coding","ncbi_id":"22894","summary":null,"start":72752169,"end":72782096,"strand":-1,"description":"DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease [Source:HGNC Symbol;Acc:HGNC:20604]"}, {"versioned_ensembl_gene_id":"ENSG00000236137.1","gene_symbol":"AL445231.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117025482,"end":117059490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206440.10","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"NFKBIL,IKBL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31537129,"end":31549080,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000109099.13","gene_symbol":"PMP22","gene_name":"peripheral myelin protein 22 [Source:HGNC Symbol;Acc:HGNC:9118]","synonyms":"GAS3,Sp110,HNPP","biotype":"protein_coding","ncbi_id":"5376","summary":"This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":15229777,"end":15265326,"strand":-1,"description":"peripheral myelin protein 22 [Source:HGNC Symbol;Acc:HGNC:9118]"}, {"versioned_ensembl_gene_id":"ENSG00000133606.10","gene_symbol":"MKRN1","gene_name":"makorin ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:7112]","synonyms":"RNF61","biotype":"protein_coding","ncbi_id":"23608","summary":"This gene encodes a protein that belongs to a novel class of zinc finger proteins. The encoded protein functions as a transcriptional co-regulator, and as an E3 ubiquitin ligase that promotes the ubiquitination and proteasomal degradation of target proteins. The protein encoded by this gene is thought to regulate RNA polymerase II-catalyzed transcription. Substrates for this protein's E3 ubiquitin ligase activity include the capsid protein of the West Nile virus and the catalytic subunit of the telomerase ribonucleoprotein. This protein controls cell cycle arrest and apoptosis by regulating p21, a cell cycle regulator, and the tumor suppressor protein p53. Pseudogenes of this gene are present on chromosomes 1, 3, 9, 12 and 20, and on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014]","start":140453040,"end":140479569,"strand":-1,"description":"makorin ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:7112]"}, {"versioned_ensembl_gene_id":"ENSG00000075891.21","gene_symbol":"PAX2","gene_name":"paired box 2 [Source:HGNC Symbol;Acc:HGNC:8616]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5076","summary":"PAX2 encodes paired box gene 2, one of many human homologues of the Drosophila melanogaster gene prd. The central feature of this transcription factor gene family is the conserved DNA-binding paired box domain. PAX2 is believed to be a target of transcriptional supression by the tumor suppressor gene WT1. Mutations within PAX2 have been shown to result in optic nerve colobomas and renal hypoplasia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":100735603,"end":100829941,"strand":1,"description":"paired box 2 [Source:HGNC Symbol;Acc:HGNC:8616]"}, {"versioned_ensembl_gene_id":"ENSG00000234057.1","gene_symbol":"CR936927.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30594716,"end":30597667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224417.2","gene_symbol":"AL606970.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":168298069,"end":168302114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115290.9","gene_symbol":"GRB14","gene_name":"growth factor receptor bound protein 14 [Source:HGNC Symbol;Acc:HGNC:4565]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2888","summary":"The product of this gene belongs to a small family of adapter proteins that are known to interact with a number of receptor tyrosine kinases and signaling molecules. This gene encodes a growth factor receptor-binding protein that interacts with insulin receptors and insulin-like growth-factor receptors. This protein likely has an inhibitory effect on receptor tyrosine kinase signaling and, in particular, on insulin receptor signaling. This gene may play a role in signaling pathways that regulate growth and metabolism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":164492812,"end":164621848,"strand":-1,"description":"growth factor receptor bound protein 14 [Source:HGNC Symbol;Acc:HGNC:4565]"}, {"versioned_ensembl_gene_id":"ENSG00000236946.2","gene_symbol":"HNRNPA1P70","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:48800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341333","summary":null,"start":68035767,"end":68036853,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:48800]"}, {"versioned_ensembl_gene_id":"ENSG00000250162.1","gene_symbol":"CSNK1A1P3","gene_name":"casein kinase 1 alpha 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38669]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526776","summary":null,"start":98833382,"end":98833711,"strand":1,"description":"casein kinase 1 alpha 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38669]"}, {"versioned_ensembl_gene_id":"ENSG00000230468.1","gene_symbol":"CLUHP5","gene_name":"clustered mitochondria homolog pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38471]","synonyms":"KIAA0664P5,KIAA0664L5","biotype":"unprocessed_pseudogene","ncbi_id":"100418745","summary":null,"start":133657235,"end":133660635,"strand":-1,"description":"clustered mitochondria homolog pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38471]"}, {"versioned_ensembl_gene_id":"ENSG00000223602.2","gene_symbol":"AC125634.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64878790,"end":64889063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271992.1","gene_symbol":"AL354872.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70445071,"end":70445536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103154.9","gene_symbol":"NECAB2","gene_name":"N-terminal EF-hand calcium binding protein 2 [Source:HGNC Symbol;Acc:HGNC:23746]","synonyms":"EFCBP2","biotype":"protein_coding","ncbi_id":"54550","summary":"The protein encoded by this gene is a neuronal calcium-binding protein that binds to and modulates the function of at least two receptors, adenosine A(2A) receptor and metabotropic glutamate receptor type 5. [provided by RefSeq, Jul 2016]","start":83968632,"end":84002776,"strand":1,"description":"N-terminal EF-hand calcium binding protein 2 [Source:HGNC Symbol;Acc:HGNC:23746]"}, {"versioned_ensembl_gene_id":"ENSG00000176783.14","gene_symbol":"RUFY1","gene_name":"RUN and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19760]","synonyms":"ZFYVE12,RABIP4,FLJ22251","biotype":"protein_coding","ncbi_id":"80230","summary":"This gene encodes a protein that contains a RUN domain and a FYVE-type zinc finger domain. The encoded protein binds to phosphatidylinositol-3-phosphate (PI3P) and plays a role in early endosomal trafficking, tethering and fusion through interactions with small GTPases including Rab4, Rab5 and Rab14. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":179550558,"end":179610026,"strand":1,"description":"RUN and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19760]"}, {"versioned_ensembl_gene_id":"ENSG00000255550.1","gene_symbol":"AP006587.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49854080,"end":49859402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147647.12","gene_symbol":"DPYS","gene_name":"dihydropyrimidinase [Source:HGNC Symbol;Acc:HGNC:3013]","synonyms":"DHPase","biotype":"protein_coding","ncbi_id":"1807","summary":"Dihydropyrimidinase catalyzes the conversion of 5,6-dihydrouracil to 3-ureidopropionate in pyrimidine metabolism. Dihydropyrimidinase is expressed at a high level in liver and kidney as a major 2.5-kb transcript and a minor 3.8-kb transcript. Defects in the DPYS gene are linked to dihydropyrimidinuria. [provided by RefSeq, Jul 2008]","start":104330324,"end":104467053,"strand":-1,"description":"dihydropyrimidinase [Source:HGNC Symbol;Acc:HGNC:3013]"}, {"versioned_ensembl_gene_id":"ENSG00000234406.1","gene_symbol":"AC004129.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25185623,"end":25188724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236534.1","gene_symbol":"H3F3BP1","gene_name":"H3 histone, family 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287087","summary":null,"start":71675067,"end":71675469,"strand":1,"description":"H3 histone, family 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42030]"}, {"versioned_ensembl_gene_id":"ENSG00000254011.1","gene_symbol":"AC011333.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":174173101,"end":174181814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145736.14","gene_symbol":"GTF2H2","gene_name":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]","synonyms":"TFIIH,T-BTF2P44,p44,BTF2P44,BTF2","biotype":"protein_coding","ncbi_id":"2966","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq, Jul 2008]","start":71032670,"end":71067689,"strand":-1,"description":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]"}, {"versioned_ensembl_gene_id":"ENSG00000273154.3","gene_symbol":"AL121845.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63708864,"end":63739103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274512.5","gene_symbol":"TBC1D3L","gene_name":"TBC1 domain family member 3L [Source:HGNC Symbol;Acc:HGNC:51246]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060376","summary":null,"start":37977972,"end":37989048,"strand":-1,"description":"TBC1 domain family member 3L [Source:HGNC Symbol;Acc:HGNC:51246]"}, {"versioned_ensembl_gene_id":"ENSG00000259620.1","gene_symbol":"AC016987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86938797,"end":86988426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255268.2","gene_symbol":"AC130364.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49824839,"end":49826724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000032389.12","gene_symbol":"EIPR1","gene_name":"EARP complex and GARP complex interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:12383]","synonyms":"TSSC1,EIPR-1","biotype":"protein_coding","ncbi_id":"7260","summary":"This gene has been reported in PMID 9403053 as one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. Alignment of this gene to genomic sequence data suggests that this gene resides on chromosome 2 rather than chromosome 11. [provided by RefSeq, Dec 2008]","start":3188925,"end":3377882,"strand":-1,"description":"EARP complex and GARP complex interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:12383]"}, {"versioned_ensembl_gene_id":"ENSG00000141985.9","gene_symbol":"SH3GL1","gene_name":"SH3 domain containing GRB2 like 1, endophilin A2 [Source:HGNC Symbol;Acc:HGNC:10830]","synonyms":"SH3D2B,MGC111371,EEN,CNSA1,SH3P8","biotype":"protein_coding","ncbi_id":"6455","summary":"This gene encodes a member of the endophilin family of Src homology 3 domain-containing proteins. The encoded protein is involved in endocytosis and may also play a role in the cell cycle. Overexpression of this gene may play a role in leukemogenesis, and the encoded protein has been implicated in acute myeloid leukemia as a fusion partner of the myeloid-lymphoid leukemia protein. Pseudogenes of this gene are located on the long arm of chromosomes 11 and 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":4360370,"end":4400547,"strand":-1,"description":"SH3 domain containing GRB2 like 1, endophilin A2 [Source:HGNC Symbol;Acc:HGNC:10830]"}, {"versioned_ensembl_gene_id":"ENSG00000253728.5","gene_symbol":"AC083841.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142834138,"end":142834940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197980.12","gene_symbol":"LEKR1","gene_name":"leucine, glutamate and lysine rich 1 [Source:HGNC Symbol;Acc:HGNC:33765]","synonyms":"FLJ16641","biotype":"protein_coding","ncbi_id":"389170","summary":null,"start":156825481,"end":157046129,"strand":1,"description":"leucine, glutamate and lysine rich 1 [Source:HGNC Symbol;Acc:HGNC:33765]"}, {"versioned_ensembl_gene_id":"ENSG00000277869.1","gene_symbol":"AL773524.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64498517,"end":64498745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271615.1","gene_symbol":"ACTG1P22","gene_name":"actin gamma 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51502]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100131953","summary":null,"start":57755428,"end":57766052,"strand":1,"description":"actin gamma 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51502]"}, {"versioned_ensembl_gene_id":"ENSG00000185056.9","gene_symbol":"C5orf47","gene_name":"chromosome 5 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:27026]","synonyms":"LOC133491","biotype":"protein_coding","ncbi_id":"133491","summary":null,"start":173973779,"end":174006140,"strand":1,"description":"chromosome 5 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:27026]"}, {"versioned_ensembl_gene_id":"ENSG00000233256.1","gene_symbol":"AL355870.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13415202,"end":13423133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234790.1","gene_symbol":"NUTF2P4","gene_name":"nuclear transport factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50453]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"128322","summary":null,"start":112748095,"end":112748475,"strand":1,"description":"nuclear transport factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50453]"}, {"versioned_ensembl_gene_id":"ENSG00000133657.14","gene_symbol":"ATP13A3","gene_name":"ATPase 13A3 [Source:HGNC Symbol;Acc:HGNC:24113]","synonyms":"AFURS1","biotype":"protein_coding","ncbi_id":"79572","summary":"ATP13A3 is a member of the P-type ATPase family of proteins that transport a variety of cations across membranes. Other P-type ATPases include ATP7B (MIM 606882) and ATP7A (MIM 300011).[supplied by OMIM, Aug 2008]","start":194402672,"end":194498364,"strand":-1,"description":"ATPase 13A3 [Source:HGNC Symbol;Acc:HGNC:24113]"}, {"versioned_ensembl_gene_id":"ENSG00000218793.1","gene_symbol":"AL049697.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87441165,"end":87442146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264028.2","gene_symbol":"RN7SL744P","gene_name":"RNA, 7SL, cytoplasmic 744, pseudogene [Source:HGNC Symbol;Acc:HGNC:46760]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479493","summary":null,"start":54344610,"end":54344876,"strand":1,"description":"RNA, 7SL, cytoplasmic 744, pseudogene [Source:HGNC Symbol;Acc:HGNC:46760]"}, {"versioned_ensembl_gene_id":"ENSG00000145794.16","gene_symbol":"MEGF10","gene_name":"multiple EGF like domains 10 [Source:HGNC Symbol;Acc:HGNC:29634]","synonyms":"KIAA1780","biotype":"protein_coding","ncbi_id":"84466","summary":"This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]","start":127290831,"end":127465737,"strand":1,"description":"multiple EGF like domains 10 [Source:HGNC Symbol;Acc:HGNC:29634]"}, {"versioned_ensembl_gene_id":"ENSG00000179520.10","gene_symbol":"SLC17A8","gene_name":"solute carrier family 17 member 8 [Source:HGNC Symbol;Acc:HGNC:20151]","synonyms":"VGLUT3,DFNA25","biotype":"protein_coding","ncbi_id":"246213","summary":"This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":100357079,"end":100422059,"strand":1,"description":"solute carrier family 17 member 8 [Source:HGNC Symbol;Acc:HGNC:20151]"}, {"versioned_ensembl_gene_id":"ENSG00000087116.14","gene_symbol":"ADAMTS2","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 2 [Source:HGNC Symbol;Acc:HGNC:218]","synonyms":"NPI,hPCPNI,ADAMTS-3,ADAM-TS2,PCINP","biotype":"protein_coding","ncbi_id":"9509","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":179110851,"end":179345430,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 2 [Source:HGNC Symbol;Acc:HGNC:218]"}, {"versioned_ensembl_gene_id":"ENSG00000167617.2","gene_symbol":"CDC42EP5","gene_name":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]","synonyms":"CEP5,Borg3","biotype":"protein_coding","ncbi_id":"148170","summary":"Cell division control protein 42 (CDC42), a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to CDC42 and regulate its function negatively. The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding. The protein may also play a role in septin organization and inducing pseudopodia formation in fibroblasts [provided by RefSeq, Jul 2013]","start":54465026,"end":54473264,"strand":-1,"description":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]"}, {"versioned_ensembl_gene_id":"ENSG00000132950.18","gene_symbol":"ZMYM5","gene_name":"zinc finger MYM-type containing 5 [Source:HGNC Symbol;Acc:HGNC:13029]","synonyms":"ZNF237,ZNF198L1,MYM","biotype":"protein_coding","ncbi_id":"9205","summary":null,"start":19823482,"end":19863636,"strand":-1,"description":"zinc finger MYM-type containing 5 [Source:HGNC Symbol;Acc:HGNC:13029]"}, {"versioned_ensembl_gene_id":"ENSG00000197329.11","gene_symbol":"PELI1","gene_name":"pellino E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:8827]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57162","summary":null,"start":64092652,"end":64144454,"strand":-1,"description":"pellino E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:8827]"}, {"versioned_ensembl_gene_id":"ENSG00000254496.1","gene_symbol":"CBX3P8","gene_name":"chromobox 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42880]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100286965","summary":null,"start":49406190,"end":49406714,"strand":1,"description":"chromobox 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42880]"}, {"versioned_ensembl_gene_id":"ENSG00000274501.1","gene_symbol":"AL121845.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63730072,"end":63730377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272321.1","gene_symbol":"AP003355.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98436669,"end":98439290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156486.7","gene_symbol":"KCNS2","gene_name":"potassium voltage-gated channel modifier subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:6301]","synonyms":"Kv9.2","biotype":"protein_coding","ncbi_id":"3788","summary":null,"start":98427022,"end":98432848,"strand":1,"description":"potassium voltage-gated channel modifier subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:6301]"}, {"versioned_ensembl_gene_id":"ENSG00000140320.11","gene_symbol":"BAHD1","gene_name":"bromo adjacent homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29153]","synonyms":"KIAA0945","biotype":"protein_coding","ncbi_id":"22893","summary":null,"start":40439721,"end":40468242,"strand":1,"description":"bromo adjacent homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29153]"}, {"versioned_ensembl_gene_id":"ENSG00000233854.1","gene_symbol":"POU6F2-AS2","gene_name":"POU6F2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:21887]","synonyms":"FLJ12971","biotype":"antisense_RNA","ncbi_id":"100689074","summary":null,"start":38984243,"end":39013551,"strand":-1,"description":"POU6F2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:21887]"}, {"versioned_ensembl_gene_id":"ENSG00000177054.13","gene_symbol":"ZDHHC13","gene_name":"zinc finger DHHC-type containing 13 [Source:HGNC Symbol;Acc:HGNC:18413]","synonyms":"FLJ10852,HIP14L,FLJ10941","biotype":"protein_coding","ncbi_id":"54503","summary":null,"start":19117099,"end":19176422,"strand":1,"description":"zinc finger DHHC-type containing 13 [Source:HGNC Symbol;Acc:HGNC:18413]"}, {"versioned_ensembl_gene_id":"ENSG00000278441.1","gene_symbol":"AC126915.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178842028,"end":178842235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228530.1","gene_symbol":"AL445687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199876978,"end":199877558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234114.8","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"HCR,C6orf18","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31134989,"end":31150760,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000049283.17","gene_symbol":"EPN3","gene_name":"epsin 3 [Source:HGNC Symbol;Acc:HGNC:18235]","synonyms":"MGC129899,FLJ20778","biotype":"protein_coding","ncbi_id":"55040","summary":null,"start":50532543,"end":50543750,"strand":1,"description":"epsin 3 [Source:HGNC Symbol;Acc:HGNC:18235]"}, {"versioned_ensembl_gene_id":"ENSG00000259417.2","gene_symbol":"CTXND1","gene_name":"cortexin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:50507]","synonyms":"LINC01314","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":80195484,"end":80252213,"strand":-1,"description":"cortexin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:50507]"}, {"versioned_ensembl_gene_id":"ENSG00000143061.17","gene_symbol":"IGSF3","gene_name":"immunoglobulin superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:5950]","synonyms":"V8,MGC117164,EWI-3","biotype":"protein_coding","ncbi_id":"3321","summary":"The protein encoded by this gene is an immunoglobulin-like membrane protein containing several V-type Ig-like domains. A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD). [provided by RefSeq, Jun 2016]","start":116574399,"end":116667755,"strand":-1,"description":"immunoglobulin superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:5950]"}, {"versioned_ensembl_gene_id":"ENSG00000227405.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31374124,"end":31374550,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000222496.1","gene_symbol":"RN7SKP200","gene_name":"RNA, 7SK small nuclear pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:45924]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480895","summary":null,"start":206221315,"end":206221634,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:45924]"}, {"versioned_ensembl_gene_id":"ENSG00000201916.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":20481158,"end":20481268,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000163564.14","gene_symbol":"PYHIN1","gene_name":"pyrin and HIN domain family member 1 [Source:HGNC Symbol;Acc:HGNC:28894]","synonyms":"MGC23885,IFIX","biotype":"protein_coding","ncbi_id":"149628","summary":"The protein encoded by this gene belongs to the HIN-200 family of interferon-inducible proteins that share a 200-amino acid signature motif at their C-termini. HIN200 proteins are primarily nuclear and are involved in transcriptional regulation of genes important for cell cycle control, differentiation, and apoptosis. Downregulation of this gene is associated with breast cancer. This protein acts as a tumor suppressor by promoting ubiquitination and subsequent degradation of MDM2, which leads to stabilization of p53/TP53. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":158930796,"end":158977054,"strand":1,"description":"pyrin and HIN domain family member 1 [Source:HGNC Symbol;Acc:HGNC:28894]"}, {"versioned_ensembl_gene_id":"ENSG00000250587.2","gene_symbol":"HPRT1P2","gene_name":"hypoxanthine phosphoribosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5160]","synonyms":"HPRTP2","biotype":"processed_pseudogene","ncbi_id":"3254","summary":null,"start":30248350,"end":30248893,"strand":1,"description":"hypoxanthine phosphoribosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5160]"}, {"versioned_ensembl_gene_id":"ENSG00000051523.10","gene_symbol":"CYBA","gene_name":"cytochrome b-245 alpha chain [Source:HGNC Symbol;Acc:HGNC:2577]","synonyms":"p22-PHOX","biotype":"protein_coding","ncbi_id":"1535","summary":"Cytochrome b is comprised of a light chain (alpha) and a heavy chain (beta). This gene encodes the light, alpha subunit which has been proposed as a primary component of the microbicidal oxidase system of phagocytes. Mutations in this gene are associated with autosomal recessive chronic granulomatous disease (CGD), that is characterized by the failure of activated phagocytes to generate superoxide, which is important for the microbicidal activity of these cells. [provided by RefSeq, Jul 2008]","start":88643283,"end":88651152,"strand":-1,"description":"cytochrome b-245 alpha chain [Source:HGNC Symbol;Acc:HGNC:2577]"}, {"versioned_ensembl_gene_id":"ENSG00000250221.1","gene_symbol":"KRT8P32","gene_name":"keratin 8 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289133","summary":null,"start":98392070,"end":98393530,"strand":-1,"description":"keratin 8 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39866]"}, {"versioned_ensembl_gene_id":"ENSG00000249257.1","gene_symbol":"AC097473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108773613,"end":108774020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249436.1","gene_symbol":"AC008780.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57614389,"end":57617431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250308.2","gene_symbol":"SALL4P1","gene_name":"spalt like transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419717","summary":null,"start":57422464,"end":57424391,"strand":1,"description":"spalt like transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39818]"}, {"versioned_ensembl_gene_id":"ENSG00000273319.1","gene_symbol":"AC058791.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130936464,"end":130939661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272720.1","gene_symbol":"AL022322.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38090127,"end":38091559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280056.1","gene_symbol":"AC097520.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92260367,"end":92260751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216813.1","gene_symbol":"AL358178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47562622,"end":47563018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258338.1","gene_symbol":"AC090680.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83171590,"end":83172740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100938.17","gene_symbol":"GMPR2","gene_name":"guanosine monophosphate reductase 2 [Source:HGNC Symbol;Acc:HGNC:4377]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51292","summary":"This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of guanosine monophosphate (GMP) to inosine monophosphate (IMP). The protein also functions in the re-utilization of free intracellular bases and purine nucleosides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":24232422,"end":24239242,"strand":1,"description":"guanosine monophosphate reductase 2 [Source:HGNC Symbol;Acc:HGNC:4377]"}, {"versioned_ensembl_gene_id":"ENSG00000249226.1","gene_symbol":"SUCLG2P4","gene_name":"succinate-CoA ligase GDP-forming beta subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43999]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130528","summary":null,"start":29001760,"end":29003357,"strand":1,"description":"succinate-CoA ligase GDP-forming beta subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43999]"}, {"versioned_ensembl_gene_id":"ENSG00000254211.5","gene_symbol":"LINC01485","gene_name":"long intergenic non-protein coding RNA 1485 [Source:HGNC Symbol;Acc:HGNC:51138]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928154","summary":null,"start":173786790,"end":173809039,"strand":-1,"description":"long intergenic non-protein coding RNA 1485 [Source:HGNC Symbol;Acc:HGNC:51138]"}, {"versioned_ensembl_gene_id":"ENSG00000254743.1","gene_symbol":"OR10V3P","gene_name":"olfactory receptor family 10 subfamily V member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15138]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81342","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59741325,"end":59742049,"strand":1,"description":"olfactory receptor family 10 subfamily V member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15138]"}, {"versioned_ensembl_gene_id":"ENSG00000253686.1","gene_symbol":"LINC01484","gene_name":"long intergenic non-protein coding RNA 1484 [Source:HGNC Symbol;Acc:HGNC:51136]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928136","summary":null,"start":173707614,"end":173746211,"strand":-1,"description":"long intergenic non-protein coding RNA 1484 [Source:HGNC Symbol;Acc:HGNC:51136]"}, {"versioned_ensembl_gene_id":"ENSG00000233192.7","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32781927,"end":32787758,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000253892.1","gene_symbol":"AC022915.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48657260,"end":48658894,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226400.2","gene_symbol":"AC010385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28927029,"end":28927284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167434.9","gene_symbol":"CA4","gene_name":"carbonic anhydrase 4 [Source:HGNC Symbol;Acc:HGNC:1375]","synonyms":"RP17,Car4,CAIV","biotype":"protein_coding","ncbi_id":"762","summary":"Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. This gene encodes a glycosylphosphatidyl-inositol-anchored membrane isozyme expressed on the luminal surfaces of pulmonary (and certain other) capillaries and proximal renal tubules. Its exact function is not known; however, it may have a role in inherited renal abnormalities of bicarbonate transport. [provided by RefSeq, Jul 2008]","start":60149936,"end":60170899,"strand":1,"description":"carbonic anhydrase 4 [Source:HGNC Symbol;Acc:HGNC:1375]"}, {"versioned_ensembl_gene_id":"ENSG00000269741.5","gene_symbol":"AC011473.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50996018,"end":51009581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267416.1","gene_symbol":"AC025048.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60079309,"end":60088695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261040.6","gene_symbol":"WFDC21P","gene_name":"WAP four-disulfide core domain 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:50357]","synonyms":"LOC645638,LNCDC,lnc-DC","biotype":"processed_transcript","ncbi_id":"645638","summary":null,"start":60083566,"end":60091885,"strand":-1,"description":"WAP four-disulfide core domain 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:50357]"}, {"versioned_ensembl_gene_id":"ENSG00000086065.13","gene_symbol":"CHMP5","gene_name":"charged multivesicular body protein 5 [Source:HGNC Symbol;Acc:HGNC:26942]","synonyms":"Vps60,SNF7DC2,HSPC177,CGI-34,C9orf83","biotype":"protein_coding","ncbi_id":"51510","summary":"CHMP5 belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":33264879,"end":33282069,"strand":1,"description":"charged multivesicular body protein 5 [Source:HGNC Symbol;Acc:HGNC:26942]"}, {"versioned_ensembl_gene_id":"ENSG00000112208.11","gene_symbol":"BAG2","gene_name":"BCL2 associated athanogene 2 [Source:HGNC Symbol;Acc:HGNC:938]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9532","summary":"BAG proteins compete with Hip for binding to the Hsc70/Hsp70 ATPase domain and promote substrate release. All the BAG proteins have an approximately 45-amino acid BAG domain near the C terminus but differ markedly in their N-terminal regions. The predicted BAG2 protein contains 211 amino acids. The BAG domains of BAG1, BAG2, and BAG3 interact specifically with the Hsc70 ATPase domain in vitro and in mammalian cells. All 3 proteins bind with high affinity to the ATPase domain of Hsc70 and inhibit its chaperone activity in a Hip-repressible manner. [provided by RefSeq, Jul 2008]","start":57172326,"end":57189833,"strand":1,"description":"BCL2 associated athanogene 2 [Source:HGNC Symbol;Acc:HGNC:938]"}, {"versioned_ensembl_gene_id":"ENSG00000164050.12","gene_symbol":"PLXNB1","gene_name":"plexin B1 [Source:HGNC Symbol;Acc:HGNC:9103]","synonyms":"SEP,PLXN5,KIAA0407","biotype":"protein_coding","ncbi_id":"5364","summary":null,"start":48403854,"end":48430051,"strand":-1,"description":"plexin B1 [Source:HGNC Symbol;Acc:HGNC:9103]"}, {"versioned_ensembl_gene_id":"ENSG00000129455.15","gene_symbol":"KLK8","gene_name":"kallikrein related peptidase 8 [Source:HGNC Symbol;Acc:HGNC:6369]","synonyms":"TADG14,PRSS19,ovasin,HNP,neuropsin","biotype":"protein_coding","ncbi_id":"11202","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in tandem in a gene cluster on chromosome 19. The encoded protein may be involved in proteolytic cascade in the skin and may serve as a biomarker for ovarian cancer. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":50996007,"end":51002711,"strand":-1,"description":"kallikrein related peptidase 8 [Source:HGNC Symbol;Acc:HGNC:6369]"}, {"versioned_ensembl_gene_id":"ENSG00000267879.1","gene_symbol":"AC011483.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50968210,"end":51012129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224131.1","gene_symbol":"CR318637.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31420428,"end":31421029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187840.4","gene_symbol":"EIF4EBP1","gene_name":"eukaryotic translation initiation factor 4E binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3288]","synonyms":"PHAS-I,4E-BP1","biotype":"protein_coding","ncbi_id":"1978","summary":"This gene encodes one member of a family of translation repressor proteins. The protein directly interacts with eukaryotic translation initiation factor 4E (eIF4E), which is a limiting component of the multisubunit complex that recruits 40S ribosomal subunits to the 5' end of mRNAs. Interaction of this protein with eIF4E inhibits complex assembly and represses translation. This protein is phosphorylated in response to various signals including UV irradiation and insulin signaling, resulting in its dissociation from eIF4E and activation of mRNA translation. [provided by RefSeq, Jul 2008]","start":38030341,"end":38060365,"strand":1,"description":"eukaryotic translation initiation factor 4E binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3288]"}, {"versioned_ensembl_gene_id":"ENSG00000154975.13","gene_symbol":"CA10","gene_name":"carbonic anhydrase 10 [Source:HGNC Symbol;Acc:HGNC:1369]","synonyms":"HUCEP-15,CARPX,CA-RPX","biotype":"protein_coding","ncbi_id":"56934","summary":"This gene encodes a protein that belongs to the carbonic anhydrase family of zinc metalloenzymes, which catalyze the reversible hydration of carbon dioxide in various biological processes. The protein encoded by this gene is an acatalytic member of the alpha-carbonic anhydrase subgroup, and it is thought to play a role in the central nervous system, especially in brain development. Multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":51630313,"end":52160017,"strand":-1,"description":"carbonic anhydrase 10 [Source:HGNC Symbol;Acc:HGNC:1369]"}, {"versioned_ensembl_gene_id":"ENSG00000240505.8","gene_symbol":"TNFRSF13B","gene_name":"TNF receptor superfamily member 13B [Source:HGNC Symbol;Acc:HGNC:18153]","synonyms":"TACI,IGAD2,CD267","biotype":"protein_coding","ncbi_id":"23495","summary":"The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":16929816,"end":16972118,"strand":-1,"description":"TNF receptor superfamily member 13B [Source:HGNC Symbol;Acc:HGNC:18153]"}, {"versioned_ensembl_gene_id":"ENSG00000251566.1","gene_symbol":"HMGB1P35","gene_name":"high mobility group box 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39175]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419950","summary":null,"start":77146568,"end":77147165,"strand":1,"description":"high mobility group box 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39175]"}, {"versioned_ensembl_gene_id":"ENSG00000128438.10","gene_symbol":"TBC1D27","gene_name":"TBC1 domain family member 27 [Source:HGNC Symbol;Acc:HGNC:28104]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"96597","summary":null,"start":16922915,"end":16934839,"strand":-1,"description":"TBC1 domain family member 27 [Source:HGNC Symbol;Acc:HGNC:28104]"}, {"versioned_ensembl_gene_id":"ENSG00000254164.1","gene_symbol":"AC008663.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173574938,"end":173576275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260306.1","gene_symbol":"AC092375.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21794095,"end":21795759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117713.18","gene_symbol":"ARID1A","gene_name":"AT-rich interaction domain 1A [Source:HGNC Symbol;Acc:HGNC:11110]","synonyms":"BAF250,B120,SMARCF1,P270,C1orf4,C10rf4,BAF250a","biotype":"protein_coding","ncbi_id":"8289","summary":"This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":26693236,"end":26782104,"strand":1,"description":"AT-rich interaction domain 1A [Source:HGNC Symbol;Acc:HGNC:11110]"}, {"versioned_ensembl_gene_id":"ENSG00000080224.17","gene_symbol":"EPHA6","gene_name":"EPH receptor A6 [Source:HGNC Symbol;Acc:HGNC:19296]","synonyms":"FLJ35246","biotype":"protein_coding","ncbi_id":"285220","summary":null,"start":96814581,"end":97752460,"strand":1,"description":"EPH receptor A6 [Source:HGNC Symbol;Acc:HGNC:19296]"}, {"versioned_ensembl_gene_id":"ENSG00000230571.2","gene_symbol":"AC113347.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26669346,"end":26669736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212373.1","gene_symbol":"RNA5SP171","gene_name":"RNA, 5S ribosomal pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:43071]","synonyms":"RN5S171","biotype":"rRNA","ncbi_id":"100873436","summary":null,"start":166918364,"end":166918478,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 171 [Source:HGNC Symbol;Acc:HGNC:43071]"}, {"versioned_ensembl_gene_id":"ENSG00000240439.3","gene_symbol":"RN7SL91P","gene_name":"RNA, 7SL, cytoplasmic 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:46107]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480946","summary":null,"start":25060649,"end":25060939,"strand":-1,"description":"RNA, 7SL, cytoplasmic 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:46107]"}, {"versioned_ensembl_gene_id":"ENSG00000179104.8","gene_symbol":"TMTC2","gene_name":"transmembrane and tetratricopeptide repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:25440]","synonyms":"DKFZp762A217","biotype":"protein_coding","ncbi_id":"160335","summary":"The protein encoded by this gene is an integral membrane protein localized to the endoplasmic reticulum (ER). The encoded protein contains many tetratricopeptide repeats, sequences known for being involved in protein-protein interactions. This protein binds both the calcium uptake pump SERCA2B and the carbohydrate-binding chaperone calnexin, and it appears to play a role in calcium homeostasis in the ER. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":82686880,"end":83134870,"strand":1,"description":"transmembrane and tetratricopeptide repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:25440]"}, {"versioned_ensembl_gene_id":"ENSG00000248426.1","gene_symbol":"AC113347.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26669711,"end":26669989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279881.1","gene_symbol":"AC041040.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48428143,"end":48431041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229247.2","gene_symbol":"AL627313.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26640377,"end":26640614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234042.1","gene_symbol":"AL591438.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63703065,"end":63703755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267475.1","gene_symbol":"AC008736.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32687089,"end":32691750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187653.11","gene_symbol":"TMSB4XP8","gene_name":"thymosin beta 4, X-linked pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:11885]","synonyms":"TMSL3","biotype":"processed_pseudogene","ncbi_id":"7117","summary":null,"start":90838903,"end":90839037,"strand":-1,"description":"thymosin beta 4, X-linked pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:11885]"}, {"versioned_ensembl_gene_id":"ENSG00000176200.1","gene_symbol":"OR4D11","gene_name":"olfactory receptor family 4 subfamily D member 11 [Source:HGNC Symbol;Acc:HGNC:15174]","synonyms":"OR4D11P","biotype":"protein_coding","ncbi_id":"219986","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59503576,"end":59504511,"strand":1,"description":"olfactory receptor family 4 subfamily D member 11 [Source:HGNC Symbol;Acc:HGNC:15174]"}, {"versioned_ensembl_gene_id":"ENSG00000167749.11","gene_symbol":"KLK4","gene_name":"kallikrein related peptidase 4 [Source:HGNC Symbol;Acc:HGNC:6365]","synonyms":"PSTS,PRSS17,KLK-L1,EMSP1,EMSP","biotype":"protein_coding","ncbi_id":"9622","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. In some tissues its expression is hormonally regulated. The expression pattern of a similar mouse protein in murine developing teeth supports a role for the protein in the degradation of enamel proteins. Several transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Dec 2014]","start":50906352,"end":50910738,"strand":-1,"description":"kallikrein related peptidase 4 [Source:HGNC Symbol;Acc:HGNC:6365]"}, {"versioned_ensembl_gene_id":"ENSG00000279419.1","gene_symbol":"AC004925.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124742312,"end":124745017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181322.13","gene_symbol":"NME9","gene_name":"NME/NM23 family member 9 [Source:HGNC Symbol;Acc:HGNC:21343]","synonyms":"TXNDC6,TXL-2,NM23-H9","biotype":"protein_coding","ncbi_id":"347736","summary":null,"start":138261437,"end":138329886,"strand":-1,"description":"NME/NM23 family member 9 [Source:HGNC Symbol;Acc:HGNC:21343]"}, {"versioned_ensembl_gene_id":"ENSG00000276841.1","gene_symbol":"AL445264.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70564267,"end":70564437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254466.2","gene_symbol":"OR4D10","gene_name":"olfactory receptor family 4 subfamily D member 10 [Source:HGNC Symbol;Acc:HGNC:15173]","synonyms":"OST711,OR4D10P","biotype":"protein_coding","ncbi_id":"390197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59473315,"end":59479361,"strand":1,"description":"olfactory receptor family 4 subfamily D member 10 [Source:HGNC Symbol;Acc:HGNC:15173]"}, {"versioned_ensembl_gene_id":"ENSG00000260997.1","gene_symbol":"AC004847.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":44958999,"end":44960909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273520.4","gene_symbol":"SPDYE8P","gene_name":"speedy/RINGO cell cycle regulator family member E8, pseudogene [Source:HGNC Symbol;Acc:HGNC:33771]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728524","summary":null,"start":73020338,"end":73029766,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E8, pseudogene [Source:HGNC Symbol;Acc:HGNC:33771]"}, {"versioned_ensembl_gene_id":"ENSG00000259165.1","gene_symbol":"AL391262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69083398,"end":69085389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256037.1","gene_symbol":"MRPL40P1","gene_name":"mitochondrial ribosomal protein L40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44532]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645328","summary":null,"start":67351436,"end":67352039,"strand":1,"description":"mitochondrial ribosomal protein L40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44532]"}, {"versioned_ensembl_gene_id":"ENSG00000260916.7","gene_symbol":"CCPG1","gene_name":"cell cycle progression 1 [Source:HGNC Symbol;Acc:HGNC:24227]","synonyms":"KIAA1254,CPR8","biotype":"protein_coding","ncbi_id":"9236","summary":null,"start":55340032,"end":55408510,"strand":-1,"description":"cell cycle progression 1 [Source:HGNC Symbol;Acc:HGNC:24227]"}, {"versioned_ensembl_gene_id":"ENSG00000267375.1","gene_symbol":"AC008649.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38683873,"end":38693606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148702.14","gene_symbol":"HABP2","gene_name":"hyaluronan binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4798]","synonyms":"PHBP,HGFAL,HABP,FSAP","biotype":"protein_coding","ncbi_id":"3026","summary":"This gene encodes a member of the peptidase S1 family of serine proteases. The encoded preproprotein is secreted by hepatocytes and proteolytically processed to generate heavy and light chains that form the mature heterodimer. Further autoproteolysis leads to smaller, inactive peptides. This extracellular protease binds hyaluronic acid and may play a role in the coagulation and fibrinolysis systems. Mutations in this gene are associated with nonmedullary thyroid cancer and susceptibility to venous thromboembolism. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":113550837,"end":113589602,"strand":1,"description":"hyaluronan binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4798]"}, {"versioned_ensembl_gene_id":"ENSG00000126091.19","gene_symbol":"ST3GAL3","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:10866]","synonyms":"SIAT6,MRT12","biotype":"protein_coding","ncbi_id":"6487","summary":"The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":43705824,"end":43931165,"strand":1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:10866]"}, {"versioned_ensembl_gene_id":"ENSG00000270722.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":145465617,"end":145465780,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000137976.7","gene_symbol":"DNASE2B","gene_name":"deoxyribonuclease 2 beta [Source:HGNC Symbol;Acc:HGNC:28875]","synonyms":"DLAD","biotype":"protein_coding","ncbi_id":"58511","summary":"The protein encoded by this gene shares considerable sequence similarity to, and is structurally related to DNase II. The latter is a well characterized endonuclease that catalyzes DNA hydrolysis in the absence of divalent cations at acidic pH. Unlike DNase II which is ubiquitously expressed, expression of this gene product is restricted to the salivary gland and lungs. The gene has been localized to chromosome 1p22.3 adjacent (and in opposite orientation) to the uricase pseudogene. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":84398532,"end":84415018,"strand":1,"description":"deoxyribonuclease 2 beta [Source:HGNC Symbol;Acc:HGNC:28875]"}, {"versioned_ensembl_gene_id":"ENSG00000233674.2","gene_symbol":"AL451062.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43743471,"end":43743741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248544.2","gene_symbol":"AC008676.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157375741,"end":157384950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123201.14","gene_symbol":"GUCY1B2","gene_name":"guanylate cyclase 1 soluble subunit beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4686]","synonyms":"GC-SB2","biotype":"transcribed_unitary_pseudogene","ncbi_id":"2974","summary":null,"start":50994511,"end":51080862,"strand":-1,"description":"guanylate cyclase 1 soluble subunit beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4686]"}, {"versioned_ensembl_gene_id":"ENSG00000261771.5","gene_symbol":"DNAAF4-CCPG1","gene_name":"DNAAF4-CCPG1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:43019]","synonyms":"DYX1C1-CCPG1","biotype":"processed_transcript","ncbi_id":"100533483","summary":"This locus represents naturally occurring read-through transcription between the neighboring dyslexia susceptibility 1 candidate 1 (DYX1C1) and cell cycle progression 1 (CCPG1) genes on chromosome 15. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":55355248,"end":55498360,"strand":-1,"description":"DNAAF4-CCPG1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:43019]"}, {"versioned_ensembl_gene_id":"ENSG00000276533.1","gene_symbol":"AC018926.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55288849,"end":55289346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118520.14","gene_symbol":"ARG1","gene_name":"arginase 1 [Source:HGNC Symbol;Acc:HGNC:663]","synonyms":null,"biotype":"protein_coding","ncbi_id":"383","summary":"Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":131573144,"end":131584332,"strand":1,"description":"arginase 1 [Source:HGNC Symbol;Acc:HGNC:663]"}, {"versioned_ensembl_gene_id":"ENSG00000278075.1","gene_symbol":"AC114341.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79900555,"end":79900903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231442.3","gene_symbol":"LARP1BP1","gene_name":"La ribonucleoprotein domain family member 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37097]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644578","summary":null,"start":63350114,"end":63351472,"strand":1,"description":"La ribonucleoprotein domain family member 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37097]"}, {"versioned_ensembl_gene_id":"ENSG00000269791.5","gene_symbol":"SSX4B","gene_name":"SSX family member 4B [Source:HGNC Symbol;Acc:HGNC:16880]","synonyms":"OTTHUMT00000056510","biotype":"protein_coding","ncbi_id":"548313","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. Chromosome Xp11 contains a segmental duplication resulting in two identical copies of synovial sarcoma, X breakpoint 4, SSX4 and SSX4B, in tail-to-tail orientation. This gene, SSX4B, represents the more centromeric copy. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":48402078,"end":48411910,"strand":-1,"description":"SSX family member 4B [Source:HGNC Symbol;Acc:HGNC:16880]"}, {"versioned_ensembl_gene_id":"ENSG00000135424.15","gene_symbol":"ITGA7","gene_name":"integrin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:6143]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3679","summary":"The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2009]","start":55684568,"end":55716043,"strand":-1,"description":"integrin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:6143]"}, {"versioned_ensembl_gene_id":"ENSG00000131263.12","gene_symbol":"RLIM","gene_name":"ring finger protein, LIM domain interacting [Source:HGNC Symbol;Acc:HGNC:13429]","synonyms":"RNF12,NY-REN-43,MGC15161","biotype":"protein_coding","ncbi_id":"51132","summary":"The protein encoded by this gene is a RING-H2 zinc finger protein. It has been shown to be an E3 ubiquitin protein ligase that targets LIM domain binding 1 (LDB1/CLIM), and causes proteasome-dependent degradation of LDB1. This protein and LDB1 are co-repressors of LHX1/LIM-1, a homeodomain transcription factor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2009]","start":74585217,"end":74614617,"strand":-1,"description":"ring finger protein, LIM domain interacting [Source:HGNC Symbol;Acc:HGNC:13429]"}, {"versioned_ensembl_gene_id":"ENSG00000068615.17","gene_symbol":"REEP1","gene_name":"receptor accessory protein 1 [Source:HGNC Symbol;Acc:HGNC:25786]","synonyms":"Yip2a,SPG31,FLJ13110,C2orf23","biotype":"protein_coding","ncbi_id":"65055","summary":"This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":86213993,"end":86338083,"strand":-1,"description":"receptor accessory protein 1 [Source:HGNC Symbol;Acc:HGNC:25786]"}, {"versioned_ensembl_gene_id":"ENSG00000248156.2","gene_symbol":"BTG4P1","gene_name":"BTG anti-proliferation factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480330","summary":null,"start":24786842,"end":24787024,"strand":-1,"description":"BTG anti-proliferation factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51544]"}, {"versioned_ensembl_gene_id":"ENSG00000226284.1","gene_symbol":"ARPC3P1","gene_name":"actin related protein 2/3 complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16092]","synonyms":"dJ470L14.3,ARPC3B","biotype":"processed_pseudogene","ncbi_id":"87171","summary":null,"start":49134480,"end":49135012,"strand":1,"description":"actin related protein 2/3 complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16092]"}, {"versioned_ensembl_gene_id":"ENSG00000123096.11","gene_symbol":"SSPN","gene_name":"sarcospan [Source:HGNC Symbol;Acc:HGNC:11322]","synonyms":"SPN2,SPN1,KRAG","biotype":"protein_coding","ncbi_id":"8082","summary":"This gene encodes a member of the dystrophin-glycoprotein complex (DGC). The DGC spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Two alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Oct 2008]","start":26121991,"end":26299290,"strand":1,"description":"sarcospan [Source:HGNC Symbol;Acc:HGNC:11322]"}, {"versioned_ensembl_gene_id":"ENSG00000135452.9","gene_symbol":"TSPAN31","gene_name":"tetraspanin 31 [Source:HGNC Symbol;Acc:HGNC:10539]","synonyms":"SAS","biotype":"protein_coding","ncbi_id":"6302","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is thought to be involved in growth-related cellular processes. This gene is associated with tumorigenesis and osteosarcoma. [provided by RefSeq, Jul 2008]","start":57738013,"end":57750211,"strand":1,"description":"tetraspanin 31 [Source:HGNC Symbol;Acc:HGNC:10539]"}, {"versioned_ensembl_gene_id":"ENSG00000276790.1","gene_symbol":"AC068234.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47279526,"end":47280047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255737.2","gene_symbol":"AGAP2-AS1","gene_name":"AGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48633]","synonyms":"PUNISHER,LOC100130776","biotype":"antisense_RNA","ncbi_id":"100130776","summary":null,"start":57726271,"end":57728356,"strand":1,"description":"AGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48633]"}, {"versioned_ensembl_gene_id":"ENSG00000234216.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32392216,"end":32393175,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000155066.15","gene_symbol":"PROM2","gene_name":"prominin 2 [Source:HGNC Symbol;Acc:HGNC:20685]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150696","summary":"This gene encodes a member of the prominin family of pentaspan membrane glycoproteins. The encoded protein localizes to basal epithelial cells and may be involved in the organization of plasma membrane microdomains. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":95274453,"end":95291308,"strand":1,"description":"prominin 2 [Source:HGNC Symbol;Acc:HGNC:20685]"}, {"versioned_ensembl_gene_id":"ENSG00000272462.2","gene_symbol":"U91328.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25992662,"end":26001775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138768.14","gene_symbol":"USO1","gene_name":"USO1 vesicle transport factor [Source:HGNC Symbol;Acc:HGNC:30904]","synonyms":"VDP,TAP,p115","biotype":"protein_coding","ncbi_id":"8615","summary":"The protein encoded by this gene is a peripheral membrane protein which recycles between the cytosol and the Golgi apparatus during interphase. It is regulated by phosphorylation: dephosphorylated protein associates with the Golgi membrane and dissociates from the membrane upon phosphorylation. Ras-associated protein 1 recruits this protein to coat protein complex II (COPII) vesicles during budding from the endoplasmic reticulum, where it interacts with a set of COPII vesicle-associated SNAREs to form a cis-SNARE complex that promotes targeting to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":75724593,"end":75814286,"strand":1,"description":"USO1 vesicle transport factor [Source:HGNC Symbol;Acc:HGNC:30904]"}, {"versioned_ensembl_gene_id":"ENSG00000112343.10","gene_symbol":"TRIM38","gene_name":"tripartite motif containing 38 [Source:HGNC Symbol;Acc:HGNC:10059]","synonyms":"RORET,RNF15","biotype":"protein_coding","ncbi_id":"10475","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The encoded protein contains a RING-type zinc finger, B box-type zinc finger and SPRY domain. The function of this protein has not been identified. A pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Jul 2012]","start":25962802,"end":25991226,"strand":1,"description":"tripartite motif containing 38 [Source:HGNC Symbol;Acc:HGNC:10059]"}, {"versioned_ensembl_gene_id":"ENSG00000231595.1","gene_symbol":"AC005224.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14210488,"end":14217922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224640.1","gene_symbol":"SRSF1P1","gene_name":"serine and arginine rich splicing factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39417]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128625","summary":null,"start":69408216,"end":69408735,"strand":-1,"description":"serine and arginine rich splicing factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39417]"}, {"versioned_ensembl_gene_id":"ENSG00000223450.1","gene_symbol":"AL590632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180000438,"end":180000808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100151.15","gene_symbol":"PICK1","gene_name":"protein interacting with PRKCA 1 [Source:HGNC Symbol;Acc:HGNC:9394]","synonyms":"dJ1039K5,PRKCABP,MGC15204","biotype":"protein_coding","ncbi_id":"9463","summary":"The protein encoded by this gene contains a PDZ domain, through which it interacts with protein kinase C, alpha (PRKCA). This protein may function as an adaptor that binds to and organizes the subcellular localization of a variety of membrane proteins. It has been shown to interact with multiple glutamate receptor subtypes, monoamine plasma membrane transporters, as well as non-voltage gated sodium channels, and may target PRKCA to these membrane proteins and thus regulate their distribution and function. This protein has also been found to act as an anchoring protein that specifically targets PRKCA to mitochondria in a ligand-specific manner. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":38056311,"end":38075701,"strand":1,"description":"protein interacting with PRKCA 1 [Source:HGNC Symbol;Acc:HGNC:9394]"}, {"versioned_ensembl_gene_id":"ENSG00000133816.13","gene_symbol":"MICAL2","gene_name":"microtubule associated monooxygenase, calponin and LIM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24693]","synonyms":"KIAA0750","biotype":"protein_coding","ncbi_id":"9645","summary":"The protein encoded by this gene is a monooxygenase that enhances depolymerization of F-actin and is therefore involved in cytoskeletal dynamics. The encoded protein is a regulator of the SRF signaling pathway. Increased expression of this gene has been associated with cancer progression and metastasis. [provided by RefSeq, Oct 2016]","start":12094008,"end":12263789,"strand":1,"description":"microtubule associated monooxygenase, calponin and LIM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24693]"}, {"versioned_ensembl_gene_id":"ENSG00000237534.1","gene_symbol":"LINC00383","gene_name":"long intergenic non-protein coding RNA 383 [Source:HGNC Symbol;Acc:HGNC:42710]","synonyms":"LINC00401","biotype":"lincRNA","ncbi_id":"103689913","summary":null,"start":69222346,"end":69292154,"strand":1,"description":"long intergenic non-protein coding RNA 383 [Source:HGNC Symbol;Acc:HGNC:42710]"}, {"versioned_ensembl_gene_id":"ENSG00000271287.1","gene_symbol":"BCRP9","gene_name":"breakpoint cluster region pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49113]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107126287","summary":null,"start":67790407,"end":67790794,"strand":1,"description":"breakpoint cluster region pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49113]"}, {"versioned_ensembl_gene_id":"ENSG00000235524.1","gene_symbol":"MTCO1P23","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52088]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075281","summary":null,"start":69591406,"end":69592931,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52088]"}, {"versioned_ensembl_gene_id":"ENSG00000231855.1","gene_symbol":"AL161935.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31628540,"end":31628599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160305.17","gene_symbol":"DIP2A","gene_name":"disco interacting protein 2 homolog A [Source:HGNC Symbol;Acc:HGNC:17217]","synonyms":"Dip2,C21orf106,KIAA0184","biotype":"protein_coding","ncbi_id":"23181","summary":"The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":46458899,"end":46569852,"strand":1,"description":"disco interacting protein 2 homolog A [Source:HGNC Symbol;Acc:HGNC:17217]"}, {"versioned_ensembl_gene_id":"ENSG00000205328.2","gene_symbol":"OR6C65","gene_name":"olfactory receptor family 6 subfamily C member 65 [Source:HGNC Symbol;Acc:HGNC:31295]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403282","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55400430,"end":55401505,"strand":1,"description":"olfactory receptor family 6 subfamily C member 65 [Source:HGNC Symbol;Acc:HGNC:31295]"}, {"versioned_ensembl_gene_id":"ENSG00000157625.15","gene_symbol":"TAB3","gene_name":"TGF-beta activated kinase 1 and MAP3K7 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:30681]","synonyms":"MAP3K7IP3","biotype":"protein_coding","ncbi_id":"257397","summary":"The product of this gene functions in the NF-kappaB signal transduction pathway. The encoded protein, and the similar and functionally redundant protein MAP3K7IP2/TAB2, forms a ternary complex with the protein kinase MAP3K7/TAK1 and either TRAF2 or TRAF6 in response to stimulation with the pro-inflammatory cytokines TNF or IL-1. Subsequent MAP3K7/TAK1 kinase activity triggers a signaling cascade leading to activation of the NF-kappaB transcription factor. The human genome contains a related pseudogene. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30827442,"end":30975084,"strand":-1,"description":"TGF-beta activated kinase 1 and MAP3K7 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:30681]"}, {"versioned_ensembl_gene_id":"ENSG00000248362.1","gene_symbol":"AC011352.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147886086,"end":147886878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136866.13","gene_symbol":"ZFP37","gene_name":"ZFP37 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12863]","synonyms":"ZNF906","biotype":"protein_coding","ncbi_id":"7539","summary":"This gene encodes a transcription factor that belongs to a large family of zinc finger proteins. A similar protein in mouse is thought to play a role in regulating the structures of the nucleolus and centromere in neurons. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":113038380,"end":113056759,"strand":-1,"description":"ZFP37 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12863]"}, {"versioned_ensembl_gene_id":"ENSG00000163328.13","gene_symbol":"GPR155","gene_name":"G protein-coupled receptor 155 [Source:HGNC Symbol;Acc:HGNC:22951]","synonyms":"PGR22,FLJ31819,DEPDC3,DEP.7","biotype":"protein_coding","ncbi_id":"151556","summary":null,"start":174431571,"end":174487094,"strand":-1,"description":"G protein-coupled receptor 155 [Source:HGNC Symbol;Acc:HGNC:22951]"}, {"versioned_ensembl_gene_id":"ENSG00000256238.1","gene_symbol":"SUPT16HP1","gene_name":"SPT16 homolog, facilitates chromatin remodeling subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31388]","synonyms":"SUPT16HP,bcm670","biotype":"processed_pseudogene","ncbi_id":"400011","summary":null,"start":16399274,"end":16402406,"strand":-1,"description":"SPT16 homolog, facilitates chromatin remodeling subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31388]"}, {"versioned_ensembl_gene_id":"ENSG00000256564.1","gene_symbol":"AC007552.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16567411,"end":16573940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079462.7","gene_symbol":"PAFAH1B3","gene_name":"platelet activating factor acetylhydrolase 1b catalytic subunit 3 [Source:HGNC Symbol;Acc:HGNC:8576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5050","summary":"This gene encodes an acetylhydrolase that catalyzes the removal of an acetyl group from the glycerol backbone of platelet-activating factor. The encoded enzyme is a subunit of the platelet-activating factor acetylhydrolase isoform 1B complex, which consists of the catalytic beta and gamma subunits and the regulatory alpha subunit. This complex functions in brain development. A translocation between this gene on chromosome 19 and the CDC-like kinase 2 gene on chromosome 1 has been observed, and was associated with cognitive disability, ataxia, and atrophy of the brain. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":42297033,"end":42303546,"strand":-1,"description":"platelet activating factor acetylhydrolase 1b catalytic subunit 3 [Source:HGNC Symbol;Acc:HGNC:8576]"}, {"versioned_ensembl_gene_id":"ENSG00000232816.1","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA70,HLA-70,HLAK","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29917230,"end":29920003,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000233852.1","gene_symbol":"AC005304.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13932720,"end":13940594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181894.14","gene_symbol":"ZNF329","gene_name":"zinc finger protein 329 [Source:HGNC Symbol;Acc:HGNC:14209]","synonyms":"FLJ12586","biotype":"protein_coding","ncbi_id":"79673","summary":null,"start":58126252,"end":58155110,"strand":-1,"description":"zinc finger protein 329 [Source:HGNC Symbol;Acc:HGNC:14209]"}, {"versioned_ensembl_gene_id":"ENSG00000174226.8","gene_symbol":"SNX31","gene_name":"sorting nexin 31 [Source:HGNC Symbol;Acc:HGNC:28605]","synonyms":"MGC39715","biotype":"protein_coding","ncbi_id":"169166","summary":null,"start":100572882,"end":100663415,"strand":-1,"description":"sorting nexin 31 [Source:HGNC Symbol;Acc:HGNC:28605]"}, {"versioned_ensembl_gene_id":"ENSG00000117707.15","gene_symbol":"PROX1","gene_name":"prospero homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9459]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5629","summary":"The protein encoded by this gene is a member of the homeobox transcription factor family. Members of this family contain a homeobox domain that consists of a 60-amino acid helix-turn-helix structure that binds DNA and RNA. The protein encoded by this gene is conserved across vertebrates and may play an essential role during development. Altered levels of this protein have been reported in cancers of different organs, such as colon, brain, blood, breast, pancreas, liver and esophagus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":213983181,"end":214041502,"strand":1,"description":"prospero homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9459]"}, {"versioned_ensembl_gene_id":"ENSG00000205312.8","gene_symbol":"KRT17P4","gene_name":"keratin 17 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50722]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339186","summary":null,"start":16847635,"end":16852777,"strand":-1,"description":"keratin 17 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50722]"}, {"versioned_ensembl_gene_id":"ENSG00000277443.2","gene_symbol":"MARCKS","gene_name":"myristoylated alanine rich protein kinase C substrate [Source:HGNC Symbol;Acc:HGNC:6759]","synonyms":"PKCSL,MACS,80K-L","biotype":"protein_coding","ncbi_id":"4082","summary":"The protein encoded by this gene is a substrate for protein kinase C. It is localized to the plasma membrane and is an actin filament crosslinking protein. Phosphorylation by protein kinase C or binding to calcium-calmodulin inhibits its association with actin and with the plasma membrane, leading to its presence in the cytoplasm. The protein is thought to be involved in cell motility, phagocytosis, membrane trafficking and mitogenesis. [provided by RefSeq, Jul 2008]","start":113857362,"end":113863471,"strand":1,"description":"myristoylated alanine rich protein kinase C substrate [Source:HGNC Symbol;Acc:HGNC:6759]"}, {"versioned_ensembl_gene_id":"ENSG00000112053.13","gene_symbol":"SLC26A8","gene_name":"solute carrier family 26 member 8 [Source:HGNC Symbol;Acc:HGNC:14468]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116369","summary":"This gene encodes a member of the SLC26 gene family of anion transporters. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. The expression of this gene appears to be restricted to spermatocytes. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2010]","start":35943514,"end":36024868,"strand":-1,"description":"solute carrier family 26 member 8 [Source:HGNC Symbol;Acc:HGNC:14468]"}, {"versioned_ensembl_gene_id":"ENSG00000267279.1","gene_symbol":"AC090409.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61585746,"end":61606916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260440.2","gene_symbol":"LINC01544","gene_name":"long intergenic non-protein coding RNA 1544 [Source:HGNC Symbol;Acc:HGNC:51312]","synonyms":"TCONS_00026194","biotype":"lincRNA","ncbi_id":"100996669","summary":null,"start":61748176,"end":61756646,"strand":1,"description":"long intergenic non-protein coding RNA 1544 [Source:HGNC Symbol;Acc:HGNC:51312]"}, {"versioned_ensembl_gene_id":"ENSG00000180279.6","gene_symbol":"LINC01869","gene_name":"long intergenic non-protein coding RNA 1869 [Source:HGNC Symbol;Acc:HGNC:25050]","synonyms":"MGC45922","biotype":"lincRNA","ncbi_id":"284365","summary":null,"start":50808874,"end":50818880,"strand":1,"description":"long intergenic non-protein coding RNA 1869 [Source:HGNC Symbol;Acc:HGNC:25050]"}, {"versioned_ensembl_gene_id":"ENSG00000250651.1","gene_symbol":"PABPC1P7","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37987]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128183","summary":null,"start":102896725,"end":102898237,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37987]"}, {"versioned_ensembl_gene_id":"ENSG00000280318.1","gene_symbol":"AC027309.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":172609094,"end":172609444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200801.1","gene_symbol":"SNORD115-28","gene_name":"small nucleolar RNA, C/D box 115-28 [Source:HGNC Symbol;Acc:HGNC:33047]","synonyms":"HBII-52-28","biotype":"snoRNA","ncbi_id":"100036565","summary":null,"start":25222348,"end":25222428,"strand":1,"description":"small nucleolar RNA, C/D box 115-28 [Source:HGNC Symbol;Acc:HGNC:33047]"}, {"versioned_ensembl_gene_id":"ENSG00000200070.1","gene_symbol":"RNU4-80P","gene_name":"RNA, U4 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:47016]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480386","summary":null,"start":59212648,"end":59212788,"strand":-1,"description":"RNA, U4 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:47016]"}, {"versioned_ensembl_gene_id":"ENSG00000164105.3","gene_symbol":"SAP30","gene_name":"Sin3A associated protein 30 [Source:HGNC Symbol;Acc:HGNC:10532]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8819","summary":"Histone acetylation plays a key role in the regulation of eukaryotic gene expression. Histone acetylation and deacetylation are catalyzed by multisubunit complexes. The protein encoded by this gene is a component of the histone deacetylase complex, which includes SIN3, SAP18, HDAC1, HDAC2, RbAp46, RbAp48, and other polypeptides. This complex is active in deacetylating core histone octamers, but inactive in deacetylating nucleosomal histones. A pseudogene of this gene is located on chromosome 3. [provided by RefSeq, Jul 2008]","start":173369969,"end":173377532,"strand":1,"description":"Sin3A associated protein 30 [Source:HGNC Symbol;Acc:HGNC:10532]"}, {"versioned_ensembl_gene_id":"ENSG00000168488.18","gene_symbol":"ATXN2L","gene_name":"ataxin 2 like [Source:HGNC Symbol;Acc:HGNC:31326]","synonyms":"A2lp,A2D","biotype":"protein_coding","ncbi_id":"11273","summary":"This gene encodes an ataxin type 2 related protein of unknown function. This protein is a member of the spinocerebellar ataxia (SCAs) family, which is associated with a complex group of neurodegenerative disorders. Several alternatively spliced transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":28823035,"end":28837237,"strand":1,"description":"ataxin 2 like [Source:HGNC Symbol;Acc:HGNC:31326]"}, {"versioned_ensembl_gene_id":"ENSG00000261488.1","gene_symbol":"AC128688.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112133423,"end":112135359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277587.1","gene_symbol":"AC008759.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9721903,"end":9722410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130540.13","gene_symbol":"SULT4A1","gene_name":"sulfotransferase family 4A member 1 [Source:HGNC Symbol;Acc:HGNC:14903]","synonyms":"SULTX3,hBR-STL-1","biotype":"protein_coding","ncbi_id":"25830","summary":"This gene encodes a member of the sulfotransferase family. The encoded protein is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizophrenia. [provided by RefSeq, Jul 2008]","start":43824509,"end":43862503,"strand":-1,"description":"sulfotransferase family 4A member 1 [Source:HGNC Symbol;Acc:HGNC:14903]"}, {"versioned_ensembl_gene_id":"ENSG00000237275.1","gene_symbol":"AL450023.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52687363,"end":52687633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113249.12","gene_symbol":"HAVCR1","gene_name":"hepatitis A virus cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:17866]","synonyms":"TIMD1,TIM1,TIM-1,KIM1,HAVCR-1,HAVCR,CD365","biotype":"protein_coding","ncbi_id":"26762","summary":"The protein encoded by this gene is a membrane receptor for both human hepatitis A virus (HHAV) and TIMD4. The encoded protein may be involved in the moderation of asthma and allergic diseases. The reference genome represents an allele that retains a MTTVP amino acid segment that confers protection against atopy in HHAV seropositive individuals. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4, 12 and 19. [provided by RefSeq, Apr 2015]","start":157029413,"end":157059119,"strand":-1,"description":"hepatitis A virus cellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:17866]"}, {"versioned_ensembl_gene_id":"ENSG00000231084.2","gene_symbol":"AL136133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185171335,"end":185171710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057468.6","gene_symbol":"MSH4","gene_name":"mutS homolog 4 [Source:HGNC Symbol;Acc:HGNC:7327]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4438","summary":"This gene encodes a member of the DNA mismatch repair mutS family. This member is a meiosis-specific protein that is not involved in DNA mismatch correction, but is required for reciprocal recombination and proper segregation of homologous chromosomes at meiosis I. This protein and MSH5 form a heterodimer which binds uniquely to a Holliday Junction and its developmental progenitor, thus provoking ADP-ATP exchange, and stabilizing the interaction between parental chromosomes during meiosis double-stranded break repair. [provided by RefSeq, Aug 2011]","start":75796882,"end":75913238,"strand":1,"description":"mutS homolog 4 [Source:HGNC Symbol;Acc:HGNC:7327]"}, {"versioned_ensembl_gene_id":"ENSG00000275866.1","gene_symbol":"AC016991.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8517364,"end":8517748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281803.1","gene_symbol":"AC136352.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21368518,"end":21370717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101109.11","gene_symbol":"STK4","gene_name":"serine/threonine kinase 4 [Source:HGNC Symbol;Acc:HGNC:11408]","synonyms":"YSK3,MST1,KRS2","biotype":"protein_coding","ncbi_id":"6789","summary":"The protein encoded by this gene is a cytoplasmic kinase that is structurally similar to the yeast Ste20p kinase, which acts upstream of the stress-induced mitogen-activated protein kinase cascade. The encoded protein can phosphorylate myelin basic protein and undergoes autophosphorylation. A caspase-cleaved fragment of the encoded protein has been shown to be capable of phosphorylating histone H2B. The particular phosphorylation catalyzed by this protein has been correlated with apoptosis, and it's possible that this protein induces the chromatin condensation observed in this process. [provided by RefSeq, Jul 2008]","start":44966474,"end":45079959,"strand":1,"description":"serine/threonine kinase 4 [Source:HGNC Symbol;Acc:HGNC:11408]"}, {"versioned_ensembl_gene_id":"ENSG00000167459.16","gene_symbol":"LINC00905","gene_name":"long intergenic non-protein coding RNA 905 [Source:HGNC Symbol;Acc:HGNC:26334]","synonyms":"FLJ25328","biotype":"processed_transcript","ncbi_id":"148231","summary":null,"start":16031307,"end":16042116,"strand":1,"description":"long intergenic non-protein coding RNA 905 [Source:HGNC Symbol;Acc:HGNC:26334]"}, {"versioned_ensembl_gene_id":"ENSG00000282107.1","gene_symbol":"TMEM255B","gene_name":"transmembrane protein 255B [Source:HGNC Symbol;Acc:HGNC:28297]","synonyms":"MGC20579,FAM70B","biotype":"protein_coding","ncbi_id":"348013","summary":null,"start":113760262,"end":113760337,"strand":1,"description":"transmembrane protein 255B [Source:HGNC Symbol;Acc:HGNC:28297]"}, {"versioned_ensembl_gene_id":"ENSG00000135698.9","gene_symbol":"MPHOSPH6","gene_name":"M-phase phosphoprotein 6 [Source:HGNC Symbol;Acc:HGNC:7214]","synonyms":"MPP6","biotype":"protein_coding","ncbi_id":"10200","summary":null,"start":82147798,"end":82170226,"strand":-1,"description":"M-phase phosphoprotein 6 [Source:HGNC Symbol;Acc:HGNC:7214]"}, {"versioned_ensembl_gene_id":"ENSG00000258989.1","gene_symbol":"AL355916.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61529128,"end":61657964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230781.1","gene_symbol":"Z83820.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":84973217,"end":84977829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276429.3","gene_symbol":"PLCH2","gene_name":"phospholipase C eta 2 [Source:HGNC Symbol;Acc:HGNC:29037]","synonyms":"PLCeta2,PLC-eta2,KIAA0450,RP3-395M20.1,PLCL4","biotype":"protein_coding","ncbi_id":"9651","summary":"PLCH2 is a member of the PLC-eta family of the phosphoinositide-specific phospholipase C (PLC) superfamily of enzymes that cleave PtdIns(4,5) P2 to generate second messengers inositol 1,4,5-trisphosphate and diacylglycerol (Zhou et al., 2005 [PubMed 16107206]).[supplied by OMIM, Jun 2009]","start":2467459,"end":2505530,"strand":1,"description":"phospholipase C eta 2 [Source:HGNC Symbol;Acc:HGNC:29037]"}, {"versioned_ensembl_gene_id":"ENSG00000272823.1","gene_symbol":"AL445423.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220828676,"end":220829211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213091.2","gene_symbol":"PHBP1","gene_name":"prohibitin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5246","summary":null,"start":150042546,"end":150043353,"strand":1,"description":"prohibitin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8913]"}, {"versioned_ensembl_gene_id":"ENSG00000254636.1","gene_symbol":"ARMS2","gene_name":"age-related maculopathy susceptibility 2 [Source:HGNC Symbol;Acc:HGNC:32685]","synonyms":"LOC387715,ARMD8","biotype":"protein_coding","ncbi_id":"387715","summary":"This gene encodes a small secreted protein specific to primates. This protein is a component of the choroidal extracellular matrix of the eye. Mutations in this gene are associated with age-related macular degeneration. [provided by RefSeq, Sep 2017]","start":122454653,"end":122457352,"strand":1,"description":"age-related maculopathy susceptibility 2 [Source:HGNC Symbol;Acc:HGNC:32685]"}, {"versioned_ensembl_gene_id":"ENSG00000219314.1","gene_symbol":"AL034372.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17381367,"end":17382120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196581.10","gene_symbol":"AJAP1","gene_name":"adherens junctions associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30801]","synonyms":"SHREW1,SHREW-1,MOT8","biotype":"protein_coding","ncbi_id":"55966","summary":null,"start":4654732,"end":4792534,"strand":1,"description":"adherens junctions associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30801]"}, {"versioned_ensembl_gene_id":"ENSG00000275219.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43296425,"end":43296615,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000264400.2","gene_symbol":"RN7SL491P","gene_name":"RNA, 7SL, cytoplasmic 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:46507]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480514","summary":null,"start":35414881,"end":35415149,"strand":-1,"description":"RNA, 7SL, cytoplasmic 491, pseudogene [Source:HGNC Symbol;Acc:HGNC:46507]"}, {"versioned_ensembl_gene_id":"ENSG00000166484.19","gene_symbol":"MAPK7","gene_name":"mitogen-activated protein kinase 7 [Source:HGNC Symbol;Acc:HGNC:6880]","synonyms":"PRKM7,ERK5,BMK1","biotype":"protein_coding","ncbi_id":"5598","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is specifically activated by mitogen-activated protein kinase kinase 5 (MAP2K5/MEK5). It is involved in the downstream signaling processes of various receptor molecules including receptor type kinases, and G protein-coupled receptors. In response to extracelluar signals, this kinase translocates to cell nucleus, where it regulates gene expression by phosphorylating, and activating different transcription factors. Four alternatively spliced transcript variants of this gene encoding two distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":19377721,"end":19383544,"strand":1,"description":"mitogen-activated protein kinase 7 [Source:HGNC Symbol;Acc:HGNC:6880]"}, {"versioned_ensembl_gene_id":"ENSG00000280607.1","gene_symbol":"AC009133.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29808679,"end":29812227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101236.16","gene_symbol":"RNF24","gene_name":"ring finger protein 24 [Source:HGNC Symbol;Acc:HGNC:13779]","synonyms":"G1L","biotype":"protein_coding","ncbi_id":"11237","summary":"This gene encodes an integral membrane protein that contains a RING-type zinc finger. The encoded protein may interact with multiple transient receptor potential cation channel subfamily C (TRPC) proteins and regulate the trafficking and insertion of these proteins into the plasma membrane. [provided by RefSeq, Mar 2016]","start":3927309,"end":4015582,"strand":-1,"description":"ring finger protein 24 [Source:HGNC Symbol;Acc:HGNC:13779]"}, {"versioned_ensembl_gene_id":"ENSG00000250493.2","gene_symbol":"AP004147.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120867933,"end":120894797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114670.13","gene_symbol":"NEK11","gene_name":"NIMA related kinase 11 [Source:HGNC Symbol;Acc:HGNC:18593]","synonyms":"FLJ23495","biotype":"protein_coding","ncbi_id":"79858","summary":"This gene encodes a member of the never in mitosis gene A family of kinases. The encoded protein localizes to the nucleoli, and may function with NEK2A in the S-phase checkpoint. The encoded protein appears to play roles in DNA replication and response to genotoxic stress. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2009]","start":131026850,"end":131350465,"strand":1,"description":"NIMA related kinase 11 [Source:HGNC Symbol;Acc:HGNC:18593]"}, {"versioned_ensembl_gene_id":"ENSG00000216966.1","gene_symbol":"AL353747.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167208631,"end":167208897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246082.2","gene_symbol":"NUDT16P1","gene_name":"nudix hydrolase 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27189]","synonyms":"NUDT16P,FLJ20525","biotype":"transcribed_unitary_pseudogene","ncbi_id":"152195","summary":null,"start":131361898,"end":131365122,"strand":1,"description":"nudix hydrolase 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27189]"}, {"versioned_ensembl_gene_id":"ENSG00000122515.14","gene_symbol":"ZMIZ2","gene_name":"zinc finger MIZ-type containing 2 [Source:HGNC Symbol;Acc:HGNC:22229]","synonyms":"ZIMP7,NET27,KIAA1886,hZIMP7,DKFZp761I2123","biotype":"protein_coding","ncbi_id":"83637","summary":"ZMIZ2 and ZMIZ1 (MIM 607159) are members of a PIAS (see MIM 603566)-like family of proteins that interact with nuclear hormone receptors. ZMIZ2 interacts with androgen receptor (AR; MIM 313700) and enhances AR-mediated transcription (Huang et al., 2005 [PubMed 16051670]).[supplied by OMIM, May 2010]","start":44748581,"end":44769881,"strand":1,"description":"zinc finger MIZ-type containing 2 [Source:HGNC Symbol;Acc:HGNC:22229]"}, {"versioned_ensembl_gene_id":"ENSG00000224752.1","gene_symbol":"VN1R21P","gene_name":"vomeronasal 1 receptor 21 pseudogene [Source:HGNC Symbol;Acc:HGNC:37336]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100128368","summary":null,"start":14089107,"end":14089871,"strand":-1,"description":"vomeronasal 1 receptor 21 pseudogene [Source:HGNC Symbol;Acc:HGNC:37336]"}, {"versioned_ensembl_gene_id":"ENSG00000280082.1","gene_symbol":"AF246928.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15346652,"end":15346738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178074.5","gene_symbol":"C2orf69","gene_name":"chromosome 2 open reading frame 69 [Source:HGNC Symbol;Acc:HGNC:26799]","synonyms":"FLJ38973","biotype":"protein_coding","ncbi_id":"205327","summary":null,"start":199911256,"end":199955935,"strand":1,"description":"chromosome 2 open reading frame 69 [Source:HGNC Symbol;Acc:HGNC:26799]"}, {"versioned_ensembl_gene_id":"ENSG00000276087.1","gene_symbol":"AC008073.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24124366,"end":24190436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205269.5","gene_symbol":"TMEM170B","gene_name":"transmembrane protein 170B [Source:HGNC Symbol;Acc:HGNC:34244]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100113407","summary":null,"start":11538278,"end":11583524,"strand":1,"description":"transmembrane protein 170B [Source:HGNC Symbol;Acc:HGNC:34244]"}, {"versioned_ensembl_gene_id":"ENSG00000110148.9","gene_symbol":"CCKBR","gene_name":"cholecystokinin B receptor [Source:HGNC Symbol;Acc:HGNC:1571]","synonyms":null,"biotype":"protein_coding","ncbi_id":"887","summary":"This gene encodes a G-protein coupled receptor for gastrin and cholecystokinin (CCK), regulatory peptides of the brain and gastrointestinal tract. This protein is a type B gastrin receptor, which has a high affinity for both sulfated and nonsulfated CCK analogs and is found principally in the central nervous system and the gastrointestinal tract. Alternative splicing results in multiple transcript variants. A misspliced transcript variant including an intron has been observed in cells from colorectal and pancreatic tumors. [provided by RefSeq, Dec 2015]","start":6259736,"end":6272127,"strand":1,"description":"cholecystokinin B receptor [Source:HGNC Symbol;Acc:HGNC:1571]"}, {"versioned_ensembl_gene_id":"ENSG00000251542.1","gene_symbol":"LINC01957","gene_name":"long intergenic non-protein coding RNA 1957 [Source:HGNC Symbol;Acc:HGNC:52783]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927059","summary":null,"start":114576041,"end":114579970,"strand":1,"description":"long intergenic non-protein coding RNA 1957 [Source:HGNC Symbol;Acc:HGNC:52783]"}, {"versioned_ensembl_gene_id":"ENSG00000246316.7","gene_symbol":"AC010230.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114488997,"end":114668410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226208.1","gene_symbol":"AL513285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70715933,"end":70720289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148400.9","gene_symbol":"NOTCH1","gene_name":"notch 1 [Source:HGNC Symbol;Acc:HGNC:7881]","synonyms":"TAN1","biotype":"protein_coding","ncbi_id":"4851","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016]","start":136494444,"end":136545862,"strand":-1,"description":"notch 1 [Source:HGNC Symbol;Acc:HGNC:7881]"}, {"versioned_ensembl_gene_id":"ENSG00000242753.1","gene_symbol":"AL445430.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11487226,"end":11515710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218020.3","gene_symbol":"THAP12P5","gene_name":"THAP domain containing 12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39569]","synonyms":"PRKRIRP5","biotype":"transcribed_processed_pseudogene","ncbi_id":"100129074","summary":null,"start":11514192,"end":11516466,"strand":1,"description":"THAP domain containing 12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39569]"}, {"versioned_ensembl_gene_id":"ENSG00000105223.19","gene_symbol":"PLD3","gene_name":"phospholipase D family member 3 [Source:HGNC Symbol;Acc:HGNC:17158]","synonyms":"HU-K4","biotype":"protein_coding","ncbi_id":"23646","summary":"This gene encodes a member of the phospholipase D (PLD) family of enzymes that catalyze the hydrolysis of membrane phospholipids. The encoded protein is a single-pass type II membrane protein and contains two PLD phosphodiesterase domains. This protein influences processing of amyloid-beta precursor protein. Mutations in this gene are associated with Alzheimer disease risk. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Apr 2014]","start":40348456,"end":40380439,"strand":1,"description":"phospholipase D family member 3 [Source:HGNC Symbol;Acc:HGNC:17158]"}, {"versioned_ensembl_gene_id":"ENSG00000279048.1","gene_symbol":"AC080080.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17940503,"end":17942922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168903.8","gene_symbol":"BTNL3","gene_name":"butyrophilin like 3 [Source:HGNC Symbol;Acc:HGNC:1143]","synonyms":"BTNLR,BTN9.1","biotype":"protein_coding","ncbi_id":"10917","summary":null,"start":180988845,"end":181006727,"strand":1,"description":"butyrophilin like 3 [Source:HGNC Symbol;Acc:HGNC:1143]"}, {"versioned_ensembl_gene_id":"ENSG00000134198.9","gene_symbol":"TSPAN2","gene_name":"tetraspanin 2 [Source:HGNC Symbol;Acc:HGNC:20659]","synonyms":"TSPAN-2,TSN2,FLJ12082","biotype":"protein_coding","ncbi_id":"10100","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":115048011,"end":115089500,"strand":-1,"description":"tetraspanin 2 [Source:HGNC Symbol;Acc:HGNC:20659]"}, {"versioned_ensembl_gene_id":"ENSG00000255333.1","gene_symbol":"AP000435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58354004,"end":58354499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270395.1","gene_symbol":"MREGP1","gene_name":"melanoregulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480304","summary":null,"start":31254361,"end":31254445,"strand":-1,"description":"melanoregulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50749]"}, {"versioned_ensembl_gene_id":"ENSG00000256079.1","gene_symbol":"AC092451.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25435581,"end":25436238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272642.1","gene_symbol":"AP003121.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127190769,"end":127223449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230442.5","gene_symbol":"AC006333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123584859,"end":123624957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197786.3","gene_symbol":"OR5B17","gene_name":"olfactory receptor family 5 subfamily B member 17 [Source:HGNC Symbol;Acc:HGNC:15267]","synonyms":"OR5B20P","biotype":"protein_coding","ncbi_id":"219965","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58358124,"end":58359069,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 17 [Source:HGNC Symbol;Acc:HGNC:15267]"}, {"versioned_ensembl_gene_id":"ENSG00000273409.2","gene_symbol":"AP003481.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127271029,"end":127337033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140365.15","gene_symbol":"COMMD4","gene_name":"COMM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26027]","synonyms":"FLJ20452","biotype":"protein_coding","ncbi_id":"54939","summary":null,"start":75335891,"end":75343224,"strand":1,"description":"COMM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26027]"}, {"versioned_ensembl_gene_id":"ENSG00000269466.2","gene_symbol":"AC233724.13","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17655129,"end":17655538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274832.1","gene_symbol":"AC233724.15","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17669283,"end":17669518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254591.1","gene_symbol":"AP003532.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127657568,"end":127657877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213540.3","gene_symbol":"AL359504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84085741,"end":84086233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233499.1","gene_symbol":"AP002345.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58365836,"end":58366763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275097.1","gene_symbol":"AC024940.5","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":31280422,"end":31280895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146809.12","gene_symbol":"ASB15","gene_name":"ankyrin repeat and SOCS box containing 15 [Source:HGNC Symbol;Acc:HGNC:19767]","synonyms":"FLJ43370","biotype":"protein_coding","ncbi_id":"142685","summary":"This gene encodes a member of the suppressor of cytokine signaling box superfamily. The proteins in this superfamily participate in the ubiquitin-proteasome system for the degradation of proteins in the cell cycle and signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":123567010,"end":123639481,"strand":1,"description":"ankyrin repeat and SOCS box containing 15 [Source:HGNC Symbol;Acc:HGNC:19767]"}, {"versioned_ensembl_gene_id":"ENSG00000256176.1","gene_symbol":"AC024940.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31311617,"end":31312029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277767.1","gene_symbol":"AL442128.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110916004,"end":110917827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241469.7","gene_symbol":"LINC00635","gene_name":"long intergenic non-protein coding RNA 635 [Source:HGNC Symbol;Acc:HGNC:27184]","synonyms":null,"biotype":"lincRNA","ncbi_id":"151658","summary":null,"start":107840228,"end":107882000,"strand":-1,"description":"long intergenic non-protein coding RNA 635 [Source:HGNC Symbol;Acc:HGNC:27184]"}, {"versioned_ensembl_gene_id":"ENSG00000250715.1","gene_symbol":"AC233724.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17670168,"end":17670571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236325.1","gene_symbol":"AC005300.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17192936,"end":17193308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139146.13","gene_symbol":"FAM60A","gene_name":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]","synonyms":"TERA,C12orf14","biotype":"protein_coding","ncbi_id":"58516","summary":null,"start":31280584,"end":31327058,"strand":-1,"description":"family with sequence similarity 60 member A [Source:HGNC Symbol;Acc:HGNC:30702]"}, {"versioned_ensembl_gene_id":"ENSG00000254612.2","gene_symbol":"AP001000.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127940913,"end":127941654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273408.1","gene_symbol":"AP002345.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58387583,"end":58388486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093072.15","gene_symbol":"ADA2","gene_name":"adenosine deaminase 2 [Source:HGNC Symbol;Acc:HGNC:1839]","synonyms":"IDGFL,CECR1,ADGF","biotype":"protein_coding","ncbi_id":"51816","summary":"This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":17178790,"end":17221989,"strand":-1,"description":"adenosine deaminase 2 [Source:HGNC Symbol;Acc:HGNC:1839]"}, {"versioned_ensembl_gene_id":"ENSG00000273415.1","gene_symbol":"AP000904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128180427,"end":128183554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142875.19","gene_symbol":"PRKACB","gene_name":"protein kinase cAMP-activated catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9381]","synonyms":"PKACb","biotype":"protein_coding","ncbi_id":"5567","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. The encoded protein is a catalytic subunit of cAMP (cyclic AMP)-dependent protein kinase, which mediates signalling though cAMP. cAMP signaling is important to a number of processes, including cell proliferaton and differentiation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2014]","start":84078062,"end":84238498,"strand":1,"description":"protein kinase cAMP-activated catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9381]"}, {"versioned_ensembl_gene_id":"ENSG00000172331.11","gene_symbol":"BPGM","gene_name":"bisphosphoglycerate mutase [Source:HGNC Symbol;Acc:HGNC:1093]","synonyms":null,"biotype":"protein_coding","ncbi_id":"669","summary":"2,3-diphosphoglycerate (2,3-DPG) is a small molecule found at high concentrations in red blood cells where it binds to and decreases the oxygen affinity of hemoglobin. This gene encodes a multifunctional enzyme that catalyzes 2,3-DPG synthesis via its synthetase activity, and 2,3-DPG degradation via its phosphatase activity. The enzyme also has phosphoglycerate phosphomutase activity. Deficiency of this enzyme increases the affinity of cells for oxygen. Mutations in this gene result in hemolytic anemia. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2009]","start":134646808,"end":134679813,"strand":1,"description":"bisphosphoglycerate mutase [Source:HGNC Symbol;Acc:HGNC:1093]"}, {"versioned_ensembl_gene_id":"ENSG00000216324.1","gene_symbol":"AL049697.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87425795,"end":87426088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272575.5","gene_symbol":"LINC02098","gene_name":"long intergenic non-protein coding RNA 2098 [Source:HGNC Symbol;Acc:HGNC:52950]","synonyms":"RP11-702B10.1","biotype":"lincRNA","ncbi_id":"105369564","summary":null,"start":128208829,"end":128241441,"strand":1,"description":"long intergenic non-protein coding RNA 2098 [Source:HGNC Symbol;Acc:HGNC:52950]"}, {"versioned_ensembl_gene_id":"ENSG00000218698.1","gene_symbol":"ST13P16","gene_name":"ST13, Hsp70 interacting protein pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38851]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422605","summary":null,"start":87444395,"end":87445175,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38851]"}, {"versioned_ensembl_gene_id":"ENSG00000256742.1","gene_symbol":"AC145422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121580792,"end":121593504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207696.1","gene_symbol":"MIR659","gene_name":"microRNA 659 [Source:HGNC Symbol;Acc:HGNC:32915]","synonyms":"MIRN659,hsa-mir-659","biotype":"miRNA","ncbi_id":"724029","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37847678,"end":37847774,"strand":-1,"description":"microRNA 659 [Source:HGNC Symbol;Acc:HGNC:32915]"}, {"versioned_ensembl_gene_id":"ENSG00000266109.1","gene_symbol":"MIR4440","gene_name":"microRNA 4440 [Source:HGNC Symbol;Acc:HGNC:41740]","synonyms":"hsa-mir-4440","biotype":"miRNA","ncbi_id":"100616397","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239068817,"end":239068914,"strand":-1,"description":"microRNA 4440 [Source:HGNC Symbol;Acc:HGNC:41740]"}, {"versioned_ensembl_gene_id":"ENSG00000207978.1","gene_symbol":"MIR154","gene_name":"microRNA 154 [Source:HGNC Symbol;Acc:HGNC:31541]","synonyms":"MIRN154,hsa-mir-154","biotype":"miRNA","ncbi_id":"406946","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101059755,"end":101059838,"strand":1,"description":"microRNA 154 [Source:HGNC Symbol;Acc:HGNC:31541]"}, {"versioned_ensembl_gene_id":"ENSG00000207813.1","gene_symbol":"MIR605","gene_name":"microRNA 605 [Source:HGNC Symbol;Acc:HGNC:32861]","synonyms":"MIRN605,hsa-mir-605","biotype":"miRNA","ncbi_id":"693190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51299573,"end":51299655,"strand":1,"description":"microRNA 605 [Source:HGNC Symbol;Acc:HGNC:32861]"}, {"versioned_ensembl_gene_id":"ENSG00000211575.3","gene_symbol":"MIR760","gene_name":"microRNA 760 [Source:HGNC Symbol;Acc:HGNC:33666]","synonyms":"MIRN760,hsa-mir-760","biotype":"miRNA","ncbi_id":"100126348","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93846832,"end":93846911,"strand":1,"description":"microRNA 760 [Source:HGNC Symbol;Acc:HGNC:33666]"}, {"versioned_ensembl_gene_id":"ENSG00000222452.1","gene_symbol":"RN7SKP59","gene_name":"RNA, 7SK small nuclear pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:45783]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479121","summary":null,"start":78165465,"end":78165778,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:45783]"}, {"versioned_ensembl_gene_id":"ENSG00000252046.1","gene_symbol":"RNU6-150P","gene_name":"RNA, U6 small nuclear 150, pseudogene [Source:HGNC Symbol;Acc:HGNC:47113]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479632","summary":null,"start":20993474,"end":20993568,"strand":-1,"description":"RNA, U6 small nuclear 150, pseudogene [Source:HGNC Symbol;Acc:HGNC:47113]"}, {"versioned_ensembl_gene_id":"ENSG00000222416.1","gene_symbol":"RNA5SP274","gene_name":"RNA, 5S ribosomal pseudogene 274 [Source:HGNC Symbol;Acc:HGNC:43174]","synonyms":"RN5S274","biotype":"rRNA","ncbi_id":"100873527","summary":null,"start":93441277,"end":93441384,"strand":1,"description":"RNA, 5S ribosomal pseudogene 274 [Source:HGNC Symbol;Acc:HGNC:43174]"}, {"versioned_ensembl_gene_id":"ENSG00000277005.1","gene_symbol":"AC006449.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38528620,"end":38528985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274716.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":179492076,"end":179492157,"strand":-1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000271254.6","gene_symbol":"AC240274.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4612,"end":29626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212319.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101628310,"end":101628406,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207512.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38505480,"end":38505581,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200806.1","gene_symbol":"RNA5SP275","gene_name":"RNA, 5S ribosomal pseudogene 275 [Source:HGNC Symbol;Acc:HGNC:43175]","synonyms":"RN5S275","biotype":"rRNA","ncbi_id":"100873528","summary":null,"start":107884494,"end":107884611,"strand":1,"description":"RNA, 5S ribosomal pseudogene 275 [Source:HGNC Symbol;Acc:HGNC:43175]"}, {"versioned_ensembl_gene_id":"ENSG00000201119.1","gene_symbol":"RNU1-33P","gene_name":"RNA, U1 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48375]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480156","summary":null,"start":145463238,"end":145463399,"strand":-1,"description":"RNA, U1 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:48375]"}, {"versioned_ensembl_gene_id":"ENSG00000222629.1","gene_symbol":"RNU2-42P","gene_name":"RNA, U2 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:48535]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481647","summary":null,"start":125890566,"end":125890678,"strand":-1,"description":"RNA, U2 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:48535]"}, {"versioned_ensembl_gene_id":"ENSG00000284147.1","gene_symbol":"MIR3150B","gene_name":"microRNA 3150b [Source:HGNC Symbol;Acc:HGNC:38938]","synonyms":"hsa-mir-3150b","biotype":"miRNA","ncbi_id":"100500907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95072911,"end":95072996,"strand":-1,"description":"microRNA 3150b [Source:HGNC Symbol;Acc:HGNC:38938]"}, {"versioned_ensembl_gene_id":"ENSG00000201549.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7784403,"end":7784511,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199151.3","gene_symbol":"MIR337","gene_name":"microRNA 337 [Source:HGNC Symbol;Acc:HGNC:31774]","synonyms":"MIRN337,hsa-mir-337","biotype":"miRNA","ncbi_id":"442905","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100874493,"end":100874585,"strand":1,"description":"microRNA 337 [Source:HGNC Symbol;Acc:HGNC:31774]"}, {"versioned_ensembl_gene_id":"ENSG00000280494.2","gene_symbol":"MIR7641-2","gene_name":"microRNA 7641-2 [Source:HGNC Symbol;Acc:HGNC:50214]","synonyms":"hsa-mir-7641-2","biotype":"miRNA","ncbi_id":"102465753","summary":"This record was withdrawn by miRBase.","start":75604209,"end":75604261,"strand":1,"description":"microRNA 7641-2 [Source:HGNC Symbol;Acc:HGNC:50214]"}, {"versioned_ensembl_gene_id":"ENSG00000274733.1","gene_symbol":"CR933783.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29064147,"end":29076673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200550.1","gene_symbol":"RNU6-137P","gene_name":"RNA, U6 small nuclear 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:47100]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481220","summary":null,"start":42712740,"end":42712847,"strand":1,"description":"RNA, U6 small nuclear 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:47100]"}, {"versioned_ensembl_gene_id":"ENSG00000252211.1","gene_symbol":"RNA5SP473","gene_name":"RNA, 5S ribosomal pseudogene 473 [Source:HGNC Symbol;Acc:HGNC:43373]","synonyms":"RN5S473","biotype":"rRNA","ncbi_id":"106479017","summary":null,"start":58363438,"end":58363562,"strand":1,"description":"RNA, 5S ribosomal pseudogene 473 [Source:HGNC Symbol;Acc:HGNC:43373]"}, {"versioned_ensembl_gene_id":"ENSG00000202144.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":19376774,"end":19376875,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000253090.2","gene_symbol":"SNORA73","gene_name":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":107985659,"end":107985773,"strand":-1,"description":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]"}, {"versioned_ensembl_gene_id":"ENSG00000199986.1","gene_symbol":"RNU6-486P","gene_name":"RNA, U6 small nuclear 486, pseudogene [Source:HGNC Symbol;Acc:HGNC:47449]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481898","summary":null,"start":180581057,"end":180581163,"strand":1,"description":"RNA, U6 small nuclear 486, pseudogene [Source:HGNC Symbol;Acc:HGNC:47449]"}, {"versioned_ensembl_gene_id":"ENSG00000265849.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31603330,"end":31603405,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000278028.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41672295,"end":41672406,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283618.1","gene_symbol":"Clostridiales-1","gene_name":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":30115845,"end":30115994,"strand":-1,"description":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]"}, {"versioned_ensembl_gene_id":"ENSG00000252053.1","gene_symbol":"RNU6-1101P","gene_name":"RNA, U6 small nuclear 1101, pseudogene [Source:HGNC Symbol;Acc:HGNC:48064]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480050","summary":null,"start":194533503,"end":194533583,"strand":-1,"description":"RNA, U6 small nuclear 1101, pseudogene [Source:HGNC Symbol;Acc:HGNC:48064]"}, {"versioned_ensembl_gene_id":"ENSG00000251934.1","gene_symbol":"RNU6-1143P","gene_name":"RNA, U6 small nuclear 1143, pseudogene [Source:HGNC Symbol;Acc:HGNC:48106]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480069","summary":null,"start":3714772,"end":3714875,"strand":-1,"description":"RNA, U6 small nuclear 1143, pseudogene [Source:HGNC Symbol;Acc:HGNC:48106]"}, {"versioned_ensembl_gene_id":"ENSG00000201145.1","gene_symbol":"RNA5SP175","gene_name":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]","synonyms":"RN5S175","biotype":"rRNA","ncbi_id":"106480758","summary":null,"start":190017696,"end":190017814,"strand":1,"description":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]"}, {"versioned_ensembl_gene_id":"ENSG00000202309.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39128826,"end":39128927,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283160.1","gene_symbol":"MIR4521","gene_name":"microRNA 4521 [Source:HGNC Symbol;Acc:HGNC:41813]","synonyms":"hsa-mir-4521","biotype":"miRNA","ncbi_id":"100616406","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8186945,"end":8187004,"strand":1,"description":"microRNA 4521 [Source:HGNC Symbol;Acc:HGNC:41813]"}, {"versioned_ensembl_gene_id":"ENSG00000207629.1","gene_symbol":"MIR526A1","gene_name":"microRNA 526a-1 [Source:HGNC Symbol;Acc:HGNC:32107]","synonyms":"MIRN526A1,MIRN526A-1,hsa-mir-526a-1","biotype":"miRNA","ncbi_id":"574475","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53706252,"end":53706336,"strand":1,"description":"microRNA 526a-1 [Source:HGNC Symbol;Acc:HGNC:32107]"}, {"versioned_ensembl_gene_id":"ENSG00000252985.1","gene_symbol":"SNORD116","gene_name":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":126426893,"end":126426970,"strand":1,"description":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]"}, {"versioned_ensembl_gene_id":"ENSG00000221411.1","gene_symbol":"MIR1227","gene_name":"microRNA 1227 [Source:HGNC Symbol;Acc:HGNC:33932]","synonyms":"MIRN1227,hsa-mir-1227","biotype":"miRNA","ncbi_id":"100302283","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2234062,"end":2234149,"strand":-1,"description":"microRNA 1227 [Source:HGNC Symbol;Acc:HGNC:33932]"}, {"versioned_ensembl_gene_id":"ENSG00000202070.1","gene_symbol":"RNU6-1175P","gene_name":"RNA, U6 small nuclear 1175, pseudogene [Source:HGNC Symbol;Acc:HGNC:48138]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480082","summary":null,"start":70075363,"end":70075469,"strand":1,"description":"RNA, U6 small nuclear 1175, pseudogene [Source:HGNC Symbol;Acc:HGNC:48138]"}, {"versioned_ensembl_gene_id":"ENSG00000284353.1","gene_symbol":"MIR142","gene_name":"microRNA 142 [Source:HGNC Symbol;Acc:HGNC:31529]","synonyms":"MIRN142,hsa-mir-142","biotype":"miRNA","ncbi_id":"406934","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58331232,"end":58331318,"strand":-1,"description":"microRNA 142 [Source:HGNC Symbol;Acc:HGNC:31529]"}, {"versioned_ensembl_gene_id":"ENSG00000212451.1","gene_symbol":"RNU11-4P","gene_name":"RNA, U11 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:46944]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481174","summary":null,"start":126671522,"end":126671654,"strand":1,"description":"RNA, U11 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:46944]"}, {"versioned_ensembl_gene_id":"ENSG00000206775.1","gene_symbol":"SNORD37","gene_name":"small nucleolar RNA, C/D box 37 [Source:HGNC Symbol;Acc:HGNC:10166]","synonyms":"RNU37,U37","biotype":"snoRNA","ncbi_id":"26812","summary":null,"start":3982507,"end":3982572,"strand":-1,"description":"small nucleolar RNA, C/D box 37 [Source:HGNC Symbol;Acc:HGNC:10166]"}, {"versioned_ensembl_gene_id":"ENSG00000238516.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28834722,"end":28834822,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274168.1","gene_symbol":"RN7SL585P","gene_name":"RNA, 7SL, cytoplasmic 585, pseudogene [Source:HGNC Symbol;Acc:HGNC:46601]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479436","summary":null,"start":94699223,"end":94699502,"strand":-1,"description":"RNA, 7SL, cytoplasmic 585, pseudogene [Source:HGNC Symbol;Acc:HGNC:46601]"}, {"versioned_ensembl_gene_id":"ENSG00000244732.3","gene_symbol":"RN7SL870P","gene_name":"RNA, 7SL, cytoplasmic 870, pseudogene [Source:HGNC Symbol;Acc:HGNC:46886]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481155","summary":null,"start":47560229,"end":47560524,"strand":-1,"description":"RNA, 7SL, cytoplasmic 870, pseudogene [Source:HGNC Symbol;Acc:HGNC:46886]"}, {"versioned_ensembl_gene_id":"ENSG00000201567.1","gene_symbol":"RNA5SP510","gene_name":"RNA, 5S ribosomal pseudogene 510 [Source:HGNC Symbol;Acc:HGNC:43410]","synonyms":"RN5S510","biotype":"rRNA","ncbi_id":"100873561","summary":null,"start":95582064,"end":95582162,"strand":1,"description":"RNA, 5S ribosomal pseudogene 510 [Source:HGNC Symbol;Acc:HGNC:43410]"}, {"versioned_ensembl_gene_id":"ENSG00000253072.1","gene_symbol":"snoMBII-202","gene_name":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15481808,"end":15481893,"strand":-1,"description":"Small nucleolar RNA MBII-202 [Source:RFAM;Acc:RF00324]"}, {"versioned_ensembl_gene_id":"ENSG00000202124.1","gene_symbol":"RNY4P3","gene_name":"RNA, Ro-associated Y4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10247]","synonyms":"hY4.F2","biotype":"misc_RNA","ncbi_id":"6089","summary":null,"start":50098264,"end":50098358,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10247]"}, {"versioned_ensembl_gene_id":"ENSG00000276197.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105287,"end":105376,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000200566.1","gene_symbol":"RNU5F-7P","gene_name":"RNA, U5F small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42524]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873834","summary":null,"start":15916189,"end":15916303,"strand":-1,"description":"RNA, U5F small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42524]"}, {"versioned_ensembl_gene_id":"ENSG00000238578.1","gene_symbol":"SNORD4A","gene_name":"small nucleolar RNA, C/D box 4A [Source:HGNC Symbol;Acc:HGNC:10097]","synonyms":"Z17A,RNU101A,mgh18S-121","biotype":"snoRNA","ncbi_id":"26773","summary":null,"start":28722582,"end":28722653,"strand":1,"description":"small nucleolar RNA, C/D box 4A [Source:HGNC Symbol;Acc:HGNC:10097]"}, {"versioned_ensembl_gene_id":"ENSG00000276886.4","gene_symbol":"GREM1","gene_name":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]","synonyms":"DAND2,DAND2,CRAC1,CRAC1,CKTSF1B1,HMPS,CKTSF1B1,HMPS,gremlin,gremlin,DRM,DRM","biotype":"protein_coding","ncbi_id":"26585","summary":"This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted glycosylated protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to relay the sonic hedgehog (SHH) signal from the polarizing region to the apical ectodermal ridge during limb bud outgrowth. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":32798311,"end":32814964,"strand":1,"description":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]"}, {"versioned_ensembl_gene_id":"ENSG00000252107.1","gene_symbol":"RNA5SP220","gene_name":"RNA, 5S ribosomal pseudogene 220 [Source:HGNC Symbol;Acc:HGNC:43120]","synonyms":"RN5S220","biotype":"rRNA","ncbi_id":"100873480","summary":null,"start":140158591,"end":140158694,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 220 [Source:HGNC Symbol;Acc:HGNC:43120]"}, {"versioned_ensembl_gene_id":"ENSG00000252045.1","gene_symbol":"SNORA33","gene_name":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]","synonyms":"ACA33","biotype":"snoRNA","ncbi_id":"594839","summary":null,"start":32538299,"end":32538434,"strand":1,"description":"Small nucleolar RNA SNORA33 [Source:RFAM;Acc:RF00438]"}, {"versioned_ensembl_gene_id":"ENSG00000200114.1","gene_symbol":"RNA5SP123","gene_name":"RNA, 5S ribosomal pseudogene 123 [Source:HGNC Symbol;Acc:HGNC:43023]","synonyms":"RN5S123","biotype":"rRNA","ncbi_id":"100873393","summary":null,"start":12511095,"end":12511213,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 123 [Source:HGNC Symbol;Acc:HGNC:43023]"}, {"versioned_ensembl_gene_id":"ENSG00000252882.1","gene_symbol":"RNU6-1137P","gene_name":"RNA, U6 small nuclear 1137, pseudogene [Source:HGNC Symbol;Acc:HGNC:48100]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480067","summary":null,"start":43395993,"end":43396091,"strand":-1,"description":"RNA, U6 small nuclear 1137, pseudogene [Source:HGNC Symbol;Acc:HGNC:48100]"}, {"versioned_ensembl_gene_id":"ENSG00000206785.1","gene_symbol":"SNORA15B-2","gene_name":"small nucleolar RNA, H/ACA box 15B-2 [Source:HGNC Symbol;Acc:HGNC:52192]","synonyms":"SNORA15C","biotype":"snoRNA","ncbi_id":"109617022","summary":null,"start":65760052,"end":65760186,"strand":1,"description":"small nucleolar RNA, H/ACA box 15B-2 [Source:HGNC Symbol;Acc:HGNC:52192]"}, {"versioned_ensembl_gene_id":"ENSG00000201071.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64111458,"end":64111569,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201675.1","gene_symbol":"SNORD32A","gene_name":"small nucleolar RNA, C/D box 32A [Source:HGNC Symbol;Acc:HGNC:10159]","synonyms":"U32A,U32,RNU32","biotype":"snoRNA","ncbi_id":"26819","summary":null,"start":49489965,"end":49490048,"strand":1,"description":"small nucleolar RNA, C/D box 32A [Source:HGNC Symbol;Acc:HGNC:10159]"}, {"versioned_ensembl_gene_id":"ENSG00000196458.10","gene_symbol":"ZNF605","gene_name":"zinc finger protein 605 [Source:HGNC Symbol;Acc:HGNC:28068]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100289635","summary":null,"start":132918308,"end":132956306,"strand":-1,"description":"zinc finger protein 605 [Source:HGNC Symbol;Acc:HGNC:28068]"}, {"versioned_ensembl_gene_id":"ENSG00000199015.4","gene_symbol":"MIR377","gene_name":"microRNA 377 [Source:HGNC Symbol;Acc:HGNC:31870]","synonyms":"MIRN377,hsa-mir-377","biotype":"miRNA","ncbi_id":"494326","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101062050,"end":101062118,"strand":1,"description":"microRNA 377 [Source:HGNC Symbol;Acc:HGNC:31870]"}, {"versioned_ensembl_gene_id":"ENSG00000265902.1","gene_symbol":"MIR4696","gene_name":"microRNA 4696 [Source:HGNC Symbol;Acc:HGNC:41780]","synonyms":"hsa-mir-4696","biotype":"miRNA","ncbi_id":"100616402","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74720268,"end":74720337,"strand":-1,"description":"microRNA 4696 [Source:HGNC Symbol;Acc:HGNC:41780]"}, {"versioned_ensembl_gene_id":"ENSG00000199968.1","gene_symbol":"SNORD115-19","gene_name":"small nucleolar RNA, C/D box 115-19 [Source:HGNC Symbol;Acc:HGNC:33038]","synonyms":"HBII-52-19","biotype":"snoRNA","ncbi_id":"100033458","summary":null,"start":25204357,"end":25204438,"strand":1,"description":"small nucleolar RNA, C/D box 115-19 [Source:HGNC Symbol;Acc:HGNC:33038]"}, {"versioned_ensembl_gene_id":"ENSG00000223136.1","gene_symbol":"RN7SKP207","gene_name":"RNA, 7SK small nuclear pseudogene 207 [Source:HGNC Symbol;Acc:HGNC:45931]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480897","summary":null,"start":29948828,"end":29949130,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 207 [Source:HGNC Symbol;Acc:HGNC:45931]"}, {"versioned_ensembl_gene_id":"ENSG00000212458.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":1118884,"end":1119013,"strand":1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000252864.1","gene_symbol":"RNA5SP278","gene_name":"RNA, 5S ribosomal pseudogene 278 [Source:HGNC Symbol;Acc:HGNC:43178]","synonyms":"RN5S278","biotype":"rRNA","ncbi_id":"100873531","summary":null,"start":140940562,"end":140940663,"strand":1,"description":"RNA, 5S ribosomal pseudogene 278 [Source:HGNC Symbol;Acc:HGNC:43178]"}, {"versioned_ensembl_gene_id":"ENSG00000207220.1","gene_symbol":"RNU1-57P","gene_name":"RNA, U1 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48399]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480166","summary":null,"start":113949917,"end":113950082,"strand":1,"description":"RNA, U1 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:48399]"}, {"versioned_ensembl_gene_id":"ENSG00000209702.1","gene_symbol":"SNORD41","gene_name":"small nucleolar RNA, C/D box 41 [Source:HGNC Symbol;Acc:HGNC:10179]","synonyms":"U41,RNU41","biotype":"snoRNA","ncbi_id":"26810","summary":null,"start":12706449,"end":12706518,"strand":-1,"description":"small nucleolar RNA, C/D box 41 [Source:HGNC Symbol;Acc:HGNC:10179]"}, {"versioned_ensembl_gene_id":"ENSG00000200041.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75181520,"end":75181621,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199809.1","gene_symbol":"RNA5SP374","gene_name":"RNA, 5S ribosomal pseudogene 374 [Source:HGNC Symbol;Acc:HGNC:43274]","synonyms":"RN5S374","biotype":"rRNA","ncbi_id":"100873632","summary":null,"start":118829681,"end":118829805,"strand":1,"description":"RNA, 5S ribosomal pseudogene 374 [Source:HGNC Symbol;Acc:HGNC:43274]"}, {"versioned_ensembl_gene_id":"ENSG00000201736.1","gene_symbol":"RNA5SP160","gene_name":"RNA, 5S ribosomal pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:43060]","synonyms":"RN5S160","biotype":"rRNA","ncbi_id":"100873426","summary":null,"start":40990154,"end":40990273,"strand":1,"description":"RNA, 5S ribosomal pseudogene 160 [Source:HGNC Symbol;Acc:HGNC:43060]"}, {"versioned_ensembl_gene_id":"ENSG00000240347.3","gene_symbol":"RN7SL35P","gene_name":"RNA, 7SL, cytoplasmic 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46051]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480931","summary":null,"start":80318253,"end":80318544,"strand":1,"description":"RNA, 7SL, cytoplasmic 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46051]"}, {"versioned_ensembl_gene_id":"ENSG00000207097.1","gene_symbol":"RNU6-614P","gene_name":"RNA, U6 small nuclear 614, pseudogene [Source:HGNC Symbol;Acc:HGNC:47577]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481375","summary":null,"start":13047583,"end":13047689,"strand":1,"description":"RNA, U6 small nuclear 614, pseudogene [Source:HGNC Symbol;Acc:HGNC:47577]"}, {"versioned_ensembl_gene_id":"ENSG00000201988.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30736304,"end":30736414,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238542.1","gene_symbol":"RNU7-104P","gene_name":"RNA, U7 small nuclear 104 pseudogene [Source:HGNC Symbol;Acc:HGNC:45638]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480448","summary":null,"start":178831371,"end":178831449,"strand":-1,"description":"RNA, U7 small nuclear 104 pseudogene [Source:HGNC Symbol;Acc:HGNC:45638]"}, {"versioned_ensembl_gene_id":"ENSG00000274484.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7474394,"end":7474494,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207000.1","gene_symbol":"RNU6-820P","gene_name":"RNA, U6 small nuclear 820, pseudogene [Source:HGNC Symbol;Acc:HGNC:47783]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479929","summary":null,"start":68935873,"end":68935979,"strand":-1,"description":"RNA, U6 small nuclear 820, pseudogene [Source:HGNC Symbol;Acc:HGNC:47783]"}, {"versioned_ensembl_gene_id":"ENSG00000281394.1","gene_symbol":"SCARNA4","gene_name":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]","synonyms":"ACA26,ACA26","biotype":"scaRNA","ncbi_id":"677771","summary":null,"start":155925958,"end":155926086,"strand":-1,"description":"small Cajal body-specific RNA 4 [Source:HGNC Symbol;Acc:HGNC:32560]"}, {"versioned_ensembl_gene_id":"ENSG00000207149.1","gene_symbol":"RNU6-465P","gene_name":"RNA, U6 small nuclear 465, pseudogene [Source:HGNC Symbol;Acc:HGNC:47428]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481326","summary":null,"start":120126974,"end":120127074,"strand":1,"description":"RNA, U6 small nuclear 465, pseudogene [Source:HGNC Symbol;Acc:HGNC:47428]"}, {"versioned_ensembl_gene_id":"ENSG00000207797.1","gene_symbol":"MIR187","gene_name":"microRNA 187 [Source:HGNC Symbol;Acc:HGNC:31558]","synonyms":"MIRN187,hsa-mir-187","biotype":"miRNA","ncbi_id":"406963","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35904818,"end":35904926,"strand":-1,"description":"microRNA 187 [Source:HGNC Symbol;Acc:HGNC:31558]"}, {"versioned_ensembl_gene_id":"ENSG00000212561.1","gene_symbol":"RNU6-381P","gene_name":"RNA, U6 small nuclear 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:47344]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480576","summary":null,"start":44066624,"end":44066731,"strand":-1,"description":"RNA, U6 small nuclear 381, pseudogene [Source:HGNC Symbol;Acc:HGNC:47344]"}, {"versioned_ensembl_gene_id":"ENSG00000280836.1","gene_symbol":"AL355480.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":45581219,"end":45581321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252652.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43331261,"end":43331356,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221753.1","gene_symbol":"MIR1273A","gene_name":"microRNA 1273a [Source:HGNC Symbol;Acc:HGNC:35340]","synonyms":"MIRN1273,MIR1273,hsa-mir-1273","biotype":"miRNA","ncbi_id":"100302165","summary":"This record was withdrawn by miRBase.","start":100023982,"end":100024084,"strand":-1,"description":"microRNA 1273a [Source:HGNC Symbol;Acc:HGNC:35340]"}, {"versioned_ensembl_gene_id":"ENSG00000264621.1","gene_symbol":"MIR5591","gene_name":"microRNA 5591 [Source:HGNC Symbol;Acc:HGNC:43531]","synonyms":"hsa-mir-5591","biotype":"miRNA","ncbi_id":"100847065","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39411910,"end":39411974,"strand":1,"description":"microRNA 5591 [Source:HGNC Symbol;Acc:HGNC:43531]"}, {"versioned_ensembl_gene_id":"ENSG00000206975.1","gene_symbol":"RNU6-13P","gene_name":"RNA, U6 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:34257]","synonyms":"RNU6-13","biotype":"snRNA","ncbi_id":"106480423","summary":null,"start":56917084,"end":56917190,"strand":1,"description":"RNA, U6 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:34257]"}, {"versioned_ensembl_gene_id":"ENSG00000202183.1","gene_symbol":"SNORA4","gene_name":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]","synonyms":"ACA4","biotype":"snoRNA","ncbi_id":"619568","summary":null,"start":82561201,"end":82561347,"strand":1,"description":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]"}, {"versioned_ensembl_gene_id":"ENSG00000207295.1","gene_symbol":"RNU6-851P","gene_name":"RNA, U6 small nuclear 851, pseudogene [Source:HGNC Symbol;Acc:HGNC:47814]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479942","summary":null,"start":38884560,"end":38884666,"strand":-1,"description":"RNA, U6 small nuclear 851, pseudogene [Source:HGNC Symbol;Acc:HGNC:47814]"}, {"versioned_ensembl_gene_id":"ENSG00000201009.1","gene_symbol":"SNORD46","gene_name":"Small nucleolar RNA SNORD46 [Source:RFAM;Acc:RF00218]","synonyms":"RNU46,RNU40,U46,U40","biotype":"snoRNA","ncbi_id":"94161","summary":null,"start":132753023,"end":132753126,"strand":1,"description":"Small nucleolar RNA SNORD46 [Source:RFAM;Acc:RF00218]"}, {"versioned_ensembl_gene_id":"ENSG00000275634.1","gene_symbol":"PART1_2","gene_name":"Prostate androgen-regulated transcript 1 conserved region 2 [Source:RFAM;Acc:RF02160]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":60488078,"end":60488327,"strand":1,"description":"Prostate androgen-regulated transcript 1 conserved region 2 [Source:RFAM;Acc:RF02160]"}, {"versioned_ensembl_gene_id":"ENSG00000206695.1","gene_symbol":"RNU6-442P","gene_name":"RNA, U6 small nuclear 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:47405]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479761","summary":null,"start":125900951,"end":125901054,"strand":1,"description":"RNA, U6 small nuclear 442, pseudogene [Source:HGNC Symbol;Acc:HGNC:47405]"}, {"versioned_ensembl_gene_id":"ENSG00000253049.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":3102913,"end":3103015,"strand":1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000275877.1","gene_symbol":"5_8S_rRNA","gene_name":"5.8S ribosomal RNA [Source:RFAM;Acc:RF00002]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":30484925,"end":30485076,"strand":-1,"description":"5.8S ribosomal RNA [Source:RFAM;Acc:RF00002]"}, {"versioned_ensembl_gene_id":"ENSG00000252101.2","gene_symbol":"RNU6-758P","gene_name":"RNA, U6 small nuclear 758, pseudogene [Source:HGNC Symbol;Acc:HGNC:47721]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481419","summary":null,"start":75286712,"end":75286800,"strand":-1,"description":"RNA, U6 small nuclear 758, pseudogene [Source:HGNC Symbol;Acc:HGNC:47721]"}, {"versioned_ensembl_gene_id":"ENSG00000277469.1","gene_symbol":"HOTTIP_3","gene_name":"HOXA transcript at the distal tip, conserved region 3 [Source:RFAM;Acc:RF02042]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27202302,"end":27202638,"strand":1,"description":"HOXA transcript at the distal tip, conserved region 3 [Source:RFAM;Acc:RF02042]"}, {"versioned_ensembl_gene_id":"ENSG00000263869.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32301118,"end":32301224,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200571.1","gene_symbol":"RNU6-1284P","gene_name":"RNA, U6 small nuclear 1284, pseudogene [Source:HGNC Symbol;Acc:HGNC:48247]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480126","summary":null,"start":136430084,"end":136430183,"strand":-1,"description":"RNA, U6 small nuclear 1284, pseudogene [Source:HGNC Symbol;Acc:HGNC:48247]"}, {"versioned_ensembl_gene_id":"ENSG00000264313.2","gene_symbol":"RN7SL644P","gene_name":"RNA, 7SL, cytoplasmic 644, pseudogene [Source:HGNC Symbol;Acc:HGNC:46660]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481853","summary":null,"start":92659044,"end":92659302,"strand":1,"description":"RNA, 7SL, cytoplasmic 644, pseudogene [Source:HGNC Symbol;Acc:HGNC:46660]"}, {"versioned_ensembl_gene_id":"ENSG00000207763.1","gene_symbol":"MIR617","gene_name":"microRNA 617 [Source:HGNC Symbol;Acc:HGNC:32873]","synonyms":"MIRN617,hsa-mir-617","biotype":"miRNA","ncbi_id":"693202","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80832533,"end":80832629,"strand":-1,"description":"microRNA 617 [Source:HGNC Symbol;Acc:HGNC:32873]"}, {"versioned_ensembl_gene_id":"ENSG00000264110.1","gene_symbol":"MIR4300","gene_name":"microRNA 4300 [Source:HGNC Symbol;Acc:HGNC:38184]","synonyms":"hsa-mir-4300","biotype":"miRNA","ncbi_id":"100422823","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81890741,"end":81890836,"strand":-1,"description":"microRNA 4300 [Source:HGNC Symbol;Acc:HGNC:38184]"}, {"versioned_ensembl_gene_id":"ENSG00000265738.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31739567,"end":31739680,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278034.1","gene_symbol":"MIR6731","gene_name":"microRNA 6731 [Source:HGNC Symbol;Acc:HGNC:50036]","synonyms":"hsa-mir-6731","biotype":"miRNA","ncbi_id":"102465437","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24919345,"end":24919416,"strand":-1,"description":"microRNA 6731 [Source:HGNC Symbol;Acc:HGNC:50036]"}, {"versioned_ensembl_gene_id":"ENSG00000241550.3","gene_symbol":"RN7SL41P","gene_name":"RNA, 7SL, cytoplasmic 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:46057]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480933","summary":null,"start":80204606,"end":80204902,"strand":1,"description":"RNA, 7SL, cytoplasmic 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:46057]"}, {"versioned_ensembl_gene_id":"ENSG00000265181.1","gene_symbol":"MIR4674","gene_name":"microRNA 4674 [Source:HGNC Symbol;Acc:HGNC:41729]","synonyms":"hsa-mir-4674","biotype":"miRNA","ncbi_id":"100616301","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136546173,"end":136546259,"strand":-1,"description":"microRNA 4674 [Source:HGNC Symbol;Acc:HGNC:41729]"}, {"versioned_ensembl_gene_id":"ENSG00000265565.1","gene_symbol":"MIR3143","gene_name":"microRNA 3143 [Source:HGNC Symbol;Acc:HGNC:38284]","synonyms":"hsa-mir-3143","biotype":"miRNA","ncbi_id":"100422934","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27147626,"end":27147688,"strand":1,"description":"microRNA 3143 [Source:HGNC Symbol;Acc:HGNC:38284]"}, {"versioned_ensembl_gene_id":"ENSG00000275165.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,SEN34L,LENG5,LENG5,SEN34,SEN34","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190866,"end":54195141,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000207869.1","gene_symbol":"MIR498","gene_name":"microRNA 498 [Source:HGNC Symbol;Acc:HGNC:32092]","synonyms":"MIRN498,hsa-mir-498","biotype":"miRNA","ncbi_id":"574460","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53674197,"end":53674320,"strand":1,"description":"microRNA 498 [Source:HGNC Symbol;Acc:HGNC:32092]"}, {"versioned_ensembl_gene_id":"ENSG00000216031.1","gene_symbol":"MIR298","gene_name":"microRNA 298 [Source:HGNC Symbol;Acc:HGNC:33634]","synonyms":"MIRN298,hsa-mir-298","biotype":"miRNA","ncbi_id":"100126296","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58818226,"end":58818313,"strand":-1,"description":"microRNA 298 [Source:HGNC Symbol;Acc:HGNC:33634]"}, {"versioned_ensembl_gene_id":"ENSG00000251715.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":72460519,"end":72460601,"strand":-1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000239182.1","gene_symbol":"SNORA35","gene_name":"Small nucleolar RNA SNORA35 [Source:RFAM;Acc:RF00566]","synonyms":"SNORA35A,HBI-36","biotype":"snoRNA","ncbi_id":"677816","summary":null,"start":118738055,"end":118738182,"strand":1,"description":"Small nucleolar RNA SNORA35 [Source:RFAM;Acc:RF00566]"}, {"versioned_ensembl_gene_id":"ENSG00000266640.1","gene_symbol":"MIR4754","gene_name":"microRNA 4754 [Source:HGNC Symbol;Acc:HGNC:41786]","synonyms":"hsa-mir-4754","biotype":"miRNA","ncbi_id":"100616168","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58386770,"end":58386858,"strand":-1,"description":"microRNA 4754 [Source:HGNC Symbol;Acc:HGNC:41786]"}, {"versioned_ensembl_gene_id":"ENSG00000199990.1","gene_symbol":"VTRNA1-1","gene_name":"vault RNA 1-1 [Source:HGNC Symbol;Acc:HGNC:12654]","synonyms":"vtRNA1-1,vRNA,VR1,VAULTRC1,HVG1,hvg-1","biotype":"misc_RNA","ncbi_id":"56664","summary":"Vaults are large cytoplasmic ribonucleoproteins of about 13 MD. They are composed of a major vault protein, MVP (MIM 605088), 2 minor vault proteins, TEP1 (MIM 601686) and PARP4 (MIM 607519), and a nontranslated RNA component, VTRNA1-1 (Kickhoefer et al., 1999 [PubMed 10551828]).[supplied by OMIM, Mar 2009]","start":140711275,"end":140711373,"strand":1,"description":"vault RNA 1-1 [Source:HGNC Symbol;Acc:HGNC:12654]"}, {"versioned_ensembl_gene_id":"ENSG00000252984.1","gene_symbol":"RNU6-844P","gene_name":"RNA, U6 small nuclear 844, pseudogene [Source:HGNC Symbol;Acc:HGNC:47807]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479939","summary":null,"start":57405074,"end":57405175,"strand":-1,"description":"RNA, U6 small nuclear 844, pseudogene [Source:HGNC Symbol;Acc:HGNC:47807]"}, {"versioned_ensembl_gene_id":"ENSG00000235253.1","gene_symbol":"AC010240.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132942932,"end":132945050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284118.1","gene_symbol":"MIR4707","gene_name":"microRNA 4707 [Source:HGNC Symbol;Acc:HGNC:41531]","synonyms":"hsa-mir-4707","biotype":"miRNA","ncbi_id":"100616424","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22956950,"end":22957029,"strand":-1,"description":"microRNA 4707 [Source:HGNC Symbol;Acc:HGNC:41531]"}, {"versioned_ensembl_gene_id":"ENSG00000274651.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31,PRP31","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000274697.1","gene_symbol":"MIR6761","gene_name":"microRNA 6761 [Source:HGNC Symbol;Acc:HGNC:49949]","synonyms":"hsa-mir-6761","biotype":"miRNA","ncbi_id":"102465456","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111799834,"end":111799905,"strand":1,"description":"microRNA 6761 [Source:HGNC Symbol;Acc:HGNC:49949]"}, {"versioned_ensembl_gene_id":"ENSG00000252363.1","gene_symbol":"RNU7-43P","gene_name":"RNA, U7 small nuclear 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:34139]","synonyms":"U7.43,RNU7-118P","biotype":"snRNA","ncbi_id":"100147830","summary":null,"start":8511125,"end":8511188,"strand":1,"description":"RNA, U7 small nuclear 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:34139]"}, {"versioned_ensembl_gene_id":"ENSG00000222107.1","gene_symbol":"RN7SKP117","gene_name":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479147","summary":null,"start":125350868,"end":125351131,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:45841]"}, {"versioned_ensembl_gene_id":"ENSG00000200179.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36203347,"end":36203459,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277583.1","gene_symbol":"ST7-AS1_2","gene_name":"ST7 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02180]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116953214,"end":116953324,"strand":1,"description":"ST7 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02180]"}, {"versioned_ensembl_gene_id":"ENSG00000264610.1","gene_symbol":"MIR4685","gene_name":"microRNA 4685 [Source:HGNC Symbol;Acc:HGNC:41802]","synonyms":"hsa-mir-4685","biotype":"miRNA","ncbi_id":"100616482","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98431292,"end":98431360,"strand":-1,"description":"microRNA 4685 [Source:HGNC Symbol;Acc:HGNC:41802]"}, {"versioned_ensembl_gene_id":"ENSG00000206850.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130906838,"end":130906949,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222251.1","gene_symbol":"RNA5SP95","gene_name":"RNA, 5S ribosomal pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:42893]","synonyms":"RN5S95","biotype":"rRNA","ncbi_id":"100873328","summary":null,"start":60998752,"end":60998888,"strand":1,"description":"RNA, 5S ribosomal pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:42893]"}, {"versioned_ensembl_gene_id":"ENSG00000239184.1","gene_symbol":"RNA5SP269","gene_name":"RNA, 5S ribosomal pseudogene 269 [Source:HGNC Symbol;Acc:HGNC:43169]","synonyms":"RN5S269","biotype":"rRNA","ncbi_id":"100873522","summary":null,"start":68695643,"end":68695779,"strand":1,"description":"RNA, 5S ribosomal pseudogene 269 [Source:HGNC Symbol;Acc:HGNC:43169]"}, {"versioned_ensembl_gene_id":"ENSG00000201876.1","gene_symbol":"RNA5SP97","gene_name":"RNA, 5S ribosomal pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:42895]","synonyms":"RN5S97","biotype":"rRNA","ncbi_id":"100873330","summary":null,"start":73968123,"end":73968206,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:42895]"}, {"versioned_ensembl_gene_id":"ENSG00000201134.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":151841736,"end":151841837,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201247.1","gene_symbol":"SNORD114-13","gene_name":"small nucleolar RNA, C/D box 114-13 [Source:HGNC Symbol;Acc:HGNC:33001]","synonyms":"14q(II-13)","biotype":"snoRNA","ncbi_id":"767591","summary":null,"start":100969879,"end":100969952,"strand":1,"description":"small nucleolar RNA, C/D box 114-13 [Source:HGNC Symbol;Acc:HGNC:33001]"}, {"versioned_ensembl_gene_id":"ENSG00000243856.3","gene_symbol":"RN7SL551P","gene_name":"RNA, 7SL, cytoplasmic 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:46567]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479422","summary":null,"start":74227506,"end":74227803,"strand":1,"description":"RNA, 7SL, cytoplasmic 551, pseudogene [Source:HGNC Symbol;Acc:HGNC:46567]"}, {"versioned_ensembl_gene_id":"ENSG00000252990.1","gene_symbol":"RNU1-54P","gene_name":"RNA, U1 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:48396]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481611","summary":null,"start":39620345,"end":39620464,"strand":-1,"description":"RNA, U1 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:48396]"}, {"versioned_ensembl_gene_id":"ENSG00000264519.2","gene_symbol":"RN7SL596P","gene_name":"RNA, 7SL, cytoplasmic 596, pseudogene [Source:HGNC Symbol;Acc:HGNC:46612]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481085","summary":null,"start":63797784,"end":63798071,"strand":-1,"description":"RNA, 7SL, cytoplasmic 596, pseudogene [Source:HGNC Symbol;Acc:HGNC:46612]"}, {"versioned_ensembl_gene_id":"ENSG00000200976.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29758758,"end":29758859,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199303.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99642237,"end":99642347,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263474.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31161534,"end":31161633,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000206937.1","gene_symbol":"SNORA70B","gene_name":"small nucleolar RNA, H/ACA box 70B [Source:HGNC Symbol;Acc:HGNC:33618]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124537","summary":null,"start":61417244,"end":61417378,"strand":-1,"description":"small nucleolar RNA, H/ACA box 70B [Source:HGNC Symbol;Acc:HGNC:33618]"}, {"versioned_ensembl_gene_id":"ENSG00000206756.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74551392,"end":74551493,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252603.1","gene_symbol":"RNU6ATAC22P","gene_name":"RNA, U6atac small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46921]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479553","summary":null,"start":41722043,"end":41722131,"strand":-1,"description":"RNA, U6atac small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46921]"}, {"versioned_ensembl_gene_id":"ENSG00000275449.1","gene_symbol":"MIR6859-3","gene_name":"microRNA 6859-3 [Source:HGNC Symbol;Acc:HGNC:50248]","synonyms":"hsa-mir-6859-3","biotype":"miRNA","ncbi_id":"102465910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101973524,"end":101973591,"strand":1,"description":"microRNA 6859-3 [Source:HGNC Symbol;Acc:HGNC:50248]"}, {"versioned_ensembl_gene_id":"ENSG00000252421.1","gene_symbol":"RNU6-1069P","gene_name":"RNA, U6 small nuclear 1069, pseudogene [Source:HGNC Symbol;Acc:HGNC:48032]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480036","summary":null,"start":31802958,"end":31803090,"strand":-1,"description":"RNA, U6 small nuclear 1069, pseudogene [Source:HGNC Symbol;Acc:HGNC:48032]"}, {"versioned_ensembl_gene_id":"ENSG00000277740.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69851148,"end":69851436,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207578.1","gene_symbol":"MIR583","gene_name":"microRNA 583 [Source:HGNC Symbol;Acc:HGNC:32839]","synonyms":"MIRN583,hsa-mir-583","biotype":"miRNA","ncbi_id":"693168","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96079138,"end":96079212,"strand":1,"description":"microRNA 583 [Source:HGNC Symbol;Acc:HGNC:32839]"}, {"versioned_ensembl_gene_id":"ENSG00000264607.1","gene_symbol":"MIR3173","gene_name":"microRNA 3173 [Source:HGNC Symbol;Acc:HGNC:38174]","synonyms":"hsa-mir-3173","biotype":"miRNA","ncbi_id":"100422981","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95137919,"end":95137986,"strand":-1,"description":"microRNA 3173 [Source:HGNC Symbol;Acc:HGNC:38174]"}, {"versioned_ensembl_gene_id":"ENSG00000238493.1","gene_symbol":"RNU6-221P","gene_name":"RNA, U6 small nuclear 221, pseudogene [Source:HGNC Symbol;Acc:HGNC:47184]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480561","summary":null,"start":55456106,"end":55456204,"strand":-1,"description":"RNA, U6 small nuclear 221, pseudogene [Source:HGNC Symbol;Acc:HGNC:47184]"}, {"versioned_ensembl_gene_id":"ENSG00000264200.1","gene_symbol":"MIR4693","gene_name":"microRNA 4693 [Source:HGNC Symbol;Acc:HGNC:41818]","synonyms":"hsa-mir-4693","biotype":"miRNA","ncbi_id":"100616457","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103849906,"end":103849980,"strand":1,"description":"microRNA 4693 [Source:HGNC Symbol;Acc:HGNC:41818]"}, {"versioned_ensembl_gene_id":"ENSG00000265653.1","gene_symbol":"MIR548AK","gene_name":"microRNA 548ak [Source:HGNC Symbol;Acc:HGNC:41893]","synonyms":"hsa-mir-548ak","biotype":"miRNA","ncbi_id":"100616488","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12130760,"end":12130816,"strand":-1,"description":"microRNA 548ak [Source:HGNC Symbol;Acc:HGNC:41893]"}, {"versioned_ensembl_gene_id":"ENSG00000201881.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72654165,"end":72654276,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201355.1","gene_symbol":"RNA5S14","gene_name":"RNA, 5S ribosomal 14 [Source:HGNC Symbol;Acc:HGNC:34375]","synonyms":"RN5S14","biotype":"rRNA","ncbi_id":"100169765","summary":null,"start":228639337,"end":228639455,"strand":-1,"description":"RNA, 5S ribosomal 14 [Source:HGNC Symbol;Acc:HGNC:34375]"}, {"versioned_ensembl_gene_id":"ENSG00000271817.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":158700691,"end":158700909,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252458.1","gene_symbol":"SNORA68","gene_name":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]","synonyms":"SNORA68A,U68,RNU68","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":159230194,"end":159230322,"strand":1,"description":"Small nucleolar RNA SNORA68 [Source:RFAM;Acc:RF00263]"}, {"versioned_ensembl_gene_id":"ENSG00000252599.1","gene_symbol":"RNU6-566P","gene_name":"RNA, U6 small nuclear 566, pseudogene [Source:HGNC Symbol;Acc:HGNC:47529]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481903","summary":null,"start":44154789,"end":44154895,"strand":-1,"description":"RNA, U6 small nuclear 566, pseudogene [Source:HGNC Symbol;Acc:HGNC:47529]"}, {"versioned_ensembl_gene_id":"ENSG00000252750.1","gene_symbol":"RNU7-70P","gene_name":"RNA, U7 small nuclear 70 pseudogene [Source:HGNC Symbol;Acc:HGNC:34166]","synonyms":"U7.70","biotype":"snRNA","ncbi_id":"100151667","summary":null,"start":112634719,"end":112634784,"strand":-1,"description":"RNA, U7 small nuclear 70 pseudogene [Source:HGNC Symbol;Acc:HGNC:34166]"}, {"versioned_ensembl_gene_id":"ENSG00000224681.1","gene_symbol":"BX664727.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40332995,"end":40333460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201014.1","gene_symbol":"RNA5SP232","gene_name":"RNA, 5S ribosomal pseudogene 232 [Source:HGNC Symbol;Acc:HGNC:43132]","synonyms":"RN5S232","biotype":"rRNA","ncbi_id":"100873490","summary":null,"start":71913738,"end":71913856,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 232 [Source:HGNC Symbol;Acc:HGNC:43132]"}, {"versioned_ensembl_gene_id":"ENSG00000252223.1","gene_symbol":"RNU6-1049P","gene_name":"RNA, U6 small nuclear 1049, pseudogene [Source:HGNC Symbol;Acc:HGNC:48012]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481779","summary":null,"start":130109204,"end":130109310,"strand":-1,"description":"RNA, U6 small nuclear 1049, pseudogene [Source:HGNC Symbol;Acc:HGNC:48012]"}, {"versioned_ensembl_gene_id":"ENSG00000207582.1","gene_symbol":"MIR30B","gene_name":"microRNA 30b [Source:HGNC Symbol;Acc:HGNC:31625]","synonyms":"MIRN30B,hsa-mir-30b","biotype":"miRNA","ncbi_id":"407030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134800520,"end":134800607,"strand":-1,"description":"microRNA 30b [Source:HGNC Symbol;Acc:HGNC:31625]"}, {"versioned_ensembl_gene_id":"ENSG00000207047.2","gene_symbol":"SNORD51","gene_name":"small nucleolar RNA, C/D box 51 [Source:HGNC Symbol;Acc:HGNC:10201]","synonyms":"RNU51,U51","biotype":"snoRNA","ncbi_id":"26798","summary":null,"start":206161878,"end":206161957,"strand":1,"description":"small nucleolar RNA, C/D box 51 [Source:HGNC Symbol;Acc:HGNC:10201]"}, {"versioned_ensembl_gene_id":"ENSG00000265813.2","gene_symbol":"RN7SL300P","gene_name":"RNA, 7SL, cytoplasmic 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:46316]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481004","summary":null,"start":153199700,"end":153200017,"strand":-1,"description":"RNA, 7SL, cytoplasmic 300, pseudogene [Source:HGNC Symbol;Acc:HGNC:46316]"}, {"versioned_ensembl_gene_id":"ENSG00000222826.1","gene_symbol":"RN7SKP286","gene_name":"RNA, 7SK small nuclear pseudogene 286 [Source:HGNC Symbol;Acc:HGNC:46010]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481822","summary":null,"start":138863597,"end":138863895,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 286 [Source:HGNC Symbol;Acc:HGNC:46010]"}, {"versioned_ensembl_gene_id":"ENSG00000263625.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31612723,"end":31612798,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000283296.1","gene_symbol":"MIR4256","gene_name":"microRNA 4256 [Source:HGNC Symbol;Acc:HGNC:38388]","synonyms":"hsa-mir-4256","biotype":"miRNA","ncbi_id":"100422976","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112461770,"end":112461833,"strand":-1,"description":"microRNA 4256 [Source:HGNC Symbol;Acc:HGNC:38388]"}, {"versioned_ensembl_gene_id":"ENSG00000240490.3","gene_symbol":"RN7SL277P","gene_name":"RNA, 7SL, cytoplasmic 277, pseudogene [Source:HGNC Symbol;Acc:HGNC:46293]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479323","summary":null,"start":19424384,"end":19424671,"strand":1,"description":"RNA, 7SL, cytoplasmic 277, pseudogene [Source:HGNC Symbol;Acc:HGNC:46293]"}, {"versioned_ensembl_gene_id":"ENSG00000200677.1","gene_symbol":"SNORD18","gene_name":"Small nucleolar RNA SNORD18 [Source:RFAM;Acc:RF00093]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":90755243,"end":90755312,"strand":-1,"description":"Small nucleolar RNA SNORD18 [Source:RFAM;Acc:RF00093]"}, {"versioned_ensembl_gene_id":"ENSG00000252096.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":4868984,"end":4869118,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000251821.1","gene_symbol":"RNU6-583P","gene_name":"RNA, U6 small nuclear 583, pseudogene [Source:HGNC Symbol;Acc:HGNC:47546]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479824","summary":null,"start":127891991,"end":127892082,"strand":1,"description":"RNA, U6 small nuclear 583, pseudogene [Source:HGNC Symbol;Acc:HGNC:47546]"}, {"versioned_ensembl_gene_id":"ENSG00000250889.2","gene_symbol":"LINC01336","gene_name":"long intergenic non-protein coding RNA 1336 [Source:HGNC Symbol;Acc:HGNC:50543]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104326191","summary":null,"start":75047719,"end":75052843,"strand":-1,"description":"long intergenic non-protein coding RNA 1336 [Source:HGNC Symbol;Acc:HGNC:50543]"}, {"versioned_ensembl_gene_id":"ENSG00000266433.6","gene_symbol":"TBC1D3P5","gene_name":"TBC1 domain family member 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43567]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440419","summary":null,"start":27417690,"end":27431623,"strand":1,"description":"TBC1 domain family member 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43567]"}, {"versioned_ensembl_gene_id":"ENSG00000173431.2","gene_symbol":"RNASE8","gene_name":"ribonuclease A family member 8 [Source:HGNC Symbol;Acc:HGNC:19277]","synonyms":"RAE2","biotype":"protein_coding","ncbi_id":"122665","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family, a subset of the ribonuclease A superfamily. The protein is expressed prominently in the placenta and exhibits antimicrobial activity against pathogenic bacteria and fungi. [provided by RefSeq, Oct 2014]","start":21057822,"end":21058455,"strand":1,"description":"ribonuclease A family member 8 [Source:HGNC Symbol;Acc:HGNC:19277]"}, {"versioned_ensembl_gene_id":"ENSG00000266529.1","gene_symbol":"MTCYBP13","gene_name":"mitochondrially encoded cytochrome b pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51975]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075129","summary":null,"start":22519617,"end":22520709,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51975]"}, {"versioned_ensembl_gene_id":"ENSG00000214900.9","gene_symbol":"LINC01588","gene_name":"long intergenic non-protein coding RNA 1588 [Source:HGNC Symbol;Acc:HGNC:27503]","synonyms":"C14orf182","biotype":"lincRNA","ncbi_id":"283551","summary":null,"start":49927571,"end":50092643,"strand":-1,"description":"long intergenic non-protein coding RNA 1588 [Source:HGNC Symbol;Acc:HGNC:27503]"}, {"versioned_ensembl_gene_id":"ENSG00000264617.1","gene_symbol":"AC233702.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21655843,"end":21657633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228607.2","gene_symbol":"CLDN25","gene_name":"claudin 25 [Source:HGNC Symbol;Acc:HGNC:37218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644672","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. [provided by RefSeq, Jun 2010]","start":113779747,"end":113780500,"strand":1,"description":"claudin 25 [Source:HGNC Symbol;Acc:HGNC:37218]"}, {"versioned_ensembl_gene_id":"ENSG00000256167.1","gene_symbol":"ATF4P4","gene_name":"activating transcription factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:787]","synonyms":"ATF4B","biotype":"transcribed_processed_pseudogene","ncbi_id":"100127952","summary":null,"start":113789231,"end":113791366,"strand":1,"description":"activating transcription factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:787]"}, {"versioned_ensembl_gene_id":"ENSG00000226330.1","gene_symbol":"AL606489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204377850,"end":204435846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159713.10","gene_symbol":"TPPP3","gene_name":"tubulin polymerization promoting protein family member 3 [Source:HGNC Symbol;Acc:HGNC:24162]","synonyms":"p25gamma,p20,CGI-38","biotype":"protein_coding","ncbi_id":"51673","summary":null,"start":67389809,"end":67393535,"strand":-1,"description":"tubulin polymerization promoting protein family member 3 [Source:HGNC Symbol;Acc:HGNC:24162]"}, {"versioned_ensembl_gene_id":"ENSG00000235082.2","gene_symbol":"SUMO1P3","gene_name":"SUMO1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"474338","summary":null,"start":160317403,"end":160317706,"strand":1,"description":"SUMO1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33150]"}, {"versioned_ensembl_gene_id":"ENSG00000237379.1","gene_symbol":"CBX1P3","gene_name":"chromobox 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38657]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128723","summary":null,"start":203954640,"end":203955780,"strand":1,"description":"chromobox 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38657]"}, {"versioned_ensembl_gene_id":"ENSG00000232917.5","gene_symbol":"HSPE1P6","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49325]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480254","summary":null,"start":203903723,"end":203904013,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49325]"}, {"versioned_ensembl_gene_id":"ENSG00000249429.1","gene_symbol":"AC016598.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143489855,"end":143531350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110200.8","gene_symbol":"ANAPC15","gene_name":"anaphase promoting complex subunit 15 [Source:HGNC Symbol;Acc:HGNC:24531]","synonyms":"HSPC020,DKFZP564M082,C11orf51,APC15","biotype":"protein_coding","ncbi_id":"25906","summary":null,"start":72106378,"end":72112780,"strand":-1,"description":"anaphase promoting complex subunit 15 [Source:HGNC Symbol;Acc:HGNC:24531]"}, {"versioned_ensembl_gene_id":"ENSG00000090061.17","gene_symbol":"CCNK","gene_name":"cyclin K [Source:HGNC Symbol;Acc:HGNC:1596]","synonyms":"CPR4","biotype":"protein_coding","ncbi_id":"8812","summary":"The protein encoded by this gene is a member of the transcription cyclin family. These cyclins may regulate transcription through their association with and activation of cyclin-dependent kinases (CDK) that phosphorylate the C-terminal domain (CTD) of the large subunit of RNA polymerase II. This gene product may play a dual role in regulating CDK and RNA polymerase II activities. [provided by RefSeq, Jul 2008]","start":99481169,"end":99535044,"strand":1,"description":"cyclin K [Source:HGNC Symbol;Acc:HGNC:1596]"}, {"versioned_ensembl_gene_id":"ENSG00000182612.10","gene_symbol":"TSPAN10","gene_name":"tetraspanin 10 [Source:HGNC Symbol;Acc:HGNC:29942]","synonyms":"OCSP","biotype":"protein_coding","ncbi_id":"83882","summary":null,"start":81637171,"end":81648749,"strand":1,"description":"tetraspanin 10 [Source:HGNC Symbol;Acc:HGNC:29942]"}, {"versioned_ensembl_gene_id":"ENSG00000213234.4","gene_symbol":"ST13P10","gene_name":"ST13, Hsp70 interacting protein pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38745]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399950","summary":null,"start":112267290,"end":112268371,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38745]"}, {"versioned_ensembl_gene_id":"ENSG00000266369.1","gene_symbol":"AC090774.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20855946,"end":20857317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156395.12","gene_symbol":"SORCS3","gene_name":"sortilin related VPS10 domain containing receptor 3 [Source:HGNC Symbol;Acc:HGNC:16699]","synonyms":"SORCS,KIAA1059","biotype":"protein_coding","ncbi_id":"22986","summary":"This gene encodes a type-I receptor transmembrane protein that is a member of the vacuolar protein sorting 10 receptor family. Proteins of this family are defined by a vacuolar protein sorting 10 domain at the N-terminus. The N-terminal segment of this domain has a consensus motif for proprotein convertase processing, and the C-terminal segment of this domain is characterized by ten conserved cysteine residues. The vacuolar protein sorting 10 domain is followed by a leucine-rich segment, a transmembrane domain, and a short C-terminal cytoplasmic domain that interacts with adaptor molecules. The transcript is expressed at high levels in the brain, and candidate gene studies suggest that genetic variation in this gene is associated with Alzheimer's disease. Consistent with this observation, knockdown of the gene in cell culture results in an increase in amyloid precursor protein processing. [provided by RefSeq, Dec 2014]","start":104641101,"end":105265235,"strand":1,"description":"sortilin related VPS10 domain containing receptor 3 [Source:HGNC Symbol;Acc:HGNC:16699]"}, {"versioned_ensembl_gene_id":"ENSG00000228395.1","gene_symbol":"AL356481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128528901,"end":128552410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168591.15","gene_symbol":"TMUB2","gene_name":"transmembrane and ubiquitin like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28459]","synonyms":"MGC3123","biotype":"protein_coding","ncbi_id":"79089","summary":null,"start":44186970,"end":44191731,"strand":1,"description":"transmembrane and ubiquitin like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28459]"}, {"versioned_ensembl_gene_id":"ENSG00000159388.5","gene_symbol":"BTG2","gene_name":"BTG anti-proliferation factor 2 [Source:HGNC Symbol;Acc:HGNC:1131]","synonyms":"TIS21,PC3,MGC126064,MGC126063,APRO1","biotype":"protein_coding","ncbi_id":"7832","summary":"The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein is involved in the regulation of the G1/S transition of the cell cycle. [provided by RefSeq, Jul 2008]","start":203305491,"end":203309602,"strand":1,"description":"BTG anti-proliferation factor 2 [Source:HGNC Symbol;Acc:HGNC:1131]"}, {"versioned_ensembl_gene_id":"ENSG00000236998.2","gene_symbol":"AL354794.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68788307,"end":68789670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154237.12","gene_symbol":"LRRK1","gene_name":"leucine rich repeat kinase 1 [Source:HGNC Symbol;Acc:HGNC:18608]","synonyms":"Roco1,RIPK6,KIAA1790,FLJ23119","biotype":"protein_coding","ncbi_id":"79705","summary":"This gene encodes a multi-domain protein that is a leucine-rich repeat kinase and a GDP/GTP binding protein. The encoded protein is thought to play a role in the regulation of bone mass. Mice lacking a similar gene showed severe osteopetrosis, increased bone mineralization and decreased bone resorption. [provided by RefSeq, Jan 2017]","start":100919215,"end":101078254,"strand":1,"description":"leucine rich repeat kinase 1 [Source:HGNC Symbol;Acc:HGNC:18608]"}, {"versioned_ensembl_gene_id":"ENSG00000107242.17","gene_symbol":"PIP5K1B","gene_name":"phosphatidylinositol-4-phosphate 5-kinase type 1 beta [Source:HGNC Symbol;Acc:HGNC:8995]","synonyms":"STM7,MSS4","biotype":"protein_coding","ncbi_id":"8395","summary":null,"start":68705414,"end":69009176,"strand":1,"description":"phosphatidylinositol-4-phosphate 5-kinase type 1 beta [Source:HGNC Symbol;Acc:HGNC:8995]"}, {"versioned_ensembl_gene_id":"ENSG00000258568.1","gene_symbol":"RHOQP1","gene_name":"ras homolog family member Q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20003]","synonyms":"RHOQP,ARHQP","biotype":"processed_pseudogene","ncbi_id":"319093","summary":null,"start":49599994,"end":49600572,"strand":1,"description":"ras homolog family member Q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20003]"}, {"versioned_ensembl_gene_id":"ENSG00000258639.1","gene_symbol":"AL359212.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48045481,"end":48046216,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244528.1","gene_symbol":"SEPT14P2","gene_name":"septin 14 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107105263","summary":null,"start":242122287,"end":242122469,"strand":1,"description":"septin 14 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51686]"}, {"versioned_ensembl_gene_id":"ENSG00000141349.8","gene_symbol":"G6PC3","gene_name":"glucose-6-phosphatase catalytic subunit 3 [Source:HGNC Symbol;Acc:HGNC:24861]","synonyms":"UGRP","biotype":"protein_coding","ncbi_id":"92579","summary":"This gene encodes the catalytic subunit of glucose-6-phosphatase (G6Pase). G6Pase is located in the endoplasmic reticulum (ER) and catalyzes the hydrolysis of glucose-6-phosphate to glucose and phosphate in the last step of the gluconeogenic and glycogenolytic pathways. Mutations in this gene result in autosomal recessive severe congenital neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":44070735,"end":44076344,"strand":1,"description":"glucose-6-phosphatase catalytic subunit 3 [Source:HGNC Symbol;Acc:HGNC:24861]"}, {"versioned_ensembl_gene_id":"ENSG00000261186.2","gene_symbol":"LINC01238","gene_name":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]","synonyms":"FLJ40615,FLJ40615","biotype":"antisense_RNA","ncbi_id":"102723927","summary":null,"start":242087351,"end":242088457,"strand":-1,"description":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]"}, {"versioned_ensembl_gene_id":"ENSG00000237911.2","gene_symbol":"SRP68P3","gene_name":"signal recognition particle 68 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30428]","synonyms":"SRPSMCR","biotype":"unprocessed_pseudogene","ncbi_id":"347717","summary":null,"start":20415792,"end":20416697,"strand":-1,"description":"signal recognition particle 68 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30428]"}, {"versioned_ensembl_gene_id":"ENSG00000225337.1","gene_symbol":"AL353608.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68307393,"end":68308445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234394.8","gene_symbol":"AL353608.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68306528,"end":68330626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154330.12","gene_symbol":"PGM5","gene_name":"phosphoglucomutase 5 [Source:HGNC Symbol;Acc:HGNC:8908]","synonyms":"PGMRP","biotype":"protein_coding","ncbi_id":"5239","summary":"Phosphoglucomutases (EC 5.2.2.2.), such as PGM5, are phosphotransferases involved in interconversion of glucose-1-phosphate and glucose-6-phosphate. PGM activity is essential in formation of carbohydrates from glucose-6-phosphate and in formation of glucose-6-phosphate from galactose and glycogen (Edwards et al., 1995 [PubMed 8586438]).[supplied by OMIM, Mar 2008]","start":68328308,"end":68531061,"strand":1,"description":"phosphoglucomutase 5 [Source:HGNC Symbol;Acc:HGNC:8908]"}, {"versioned_ensembl_gene_id":"ENSG00000229019.1","gene_symbol":"AL161457.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68426843,"end":68429369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188735.12","gene_symbol":"TMEM120B","gene_name":"transmembrane protein 120B [Source:HGNC Symbol;Acc:HGNC:32008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144404","summary":null,"start":121712752,"end":121783001,"strand":1,"description":"transmembrane protein 120B [Source:HGNC Symbol;Acc:HGNC:32008]"}, {"versioned_ensembl_gene_id":"ENSG00000259525.1","gene_symbol":"GCSHP2","gene_name":"glycine cleavage system protein H pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288298","summary":null,"start":103184204,"end":103185039,"strand":1,"description":"glycine cleavage system protein H pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43927]"}, {"versioned_ensembl_gene_id":"ENSG00000133048.12","gene_symbol":"CHI3L1","gene_name":"chitinase 3 like 1 [Source:HGNC Symbol;Acc:HGNC:1932]","synonyms":"YKL40,GP39","biotype":"protein_coding","ncbi_id":"1116","summary":"Chitinases catalyze the hydrolysis of chitin, which is an abundant glycopolymer found in insect exoskeletons and fungal cell walls. The glycoside hydrolase 18 family of chitinases includes eight human family members. This gene encodes a glycoprotein member of the glycosyl hydrolase 18 family. The protein lacks chitinase activity and is secreted by activated macrophages, chondrocytes, neutrophils and synovial cells. The protein is thought to play a role in the process of inflammation and tissue remodeling. [provided by RefSeq, Sep 2009]","start":203178931,"end":203186749,"strand":-1,"description":"chitinase 3 like 1 [Source:HGNC Symbol;Acc:HGNC:1932]"}, {"versioned_ensembl_gene_id":"ENSG00000187559.5","gene_symbol":"FOXD4L3","gene_name":"forkhead box D4 like 3 [Source:HGNC Symbol;Acc:HGNC:18523]","synonyms":"OTTHUMG00000019959,FOXD6","biotype":"protein_coding","ncbi_id":"286380","summary":null,"start":68302867,"end":68304905,"strand":1,"description":"forkhead box D4 like 3 [Source:HGNC Symbol;Acc:HGNC:18523]"}, {"versioned_ensembl_gene_id":"ENSG00000220091.2","gene_symbol":"LAP3P1","gene_name":"leucine aminopeptidase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873864","summary":null,"start":82924829,"end":82925122,"strand":-1,"description":"leucine aminopeptidase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42364]"}, {"versioned_ensembl_gene_id":"ENSG00000227215.1","gene_symbol":"AL355613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82932601,"end":82938677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122483.17","gene_symbol":"CCDC18","gene_name":"coiled-coil domain containing 18 [Source:HGNC Symbol;Acc:HGNC:30370]","synonyms":"NY-SAR-41","biotype":"protein_coding","ncbi_id":"343099","summary":null,"start":93179919,"end":93278730,"strand":1,"description":"coiled-coil domain containing 18 [Source:HGNC Symbol;Acc:HGNC:30370]"}, {"versioned_ensembl_gene_id":"ENSG00000105617.3","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54155161,"end":54159882,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000188508.10","gene_symbol":"KRTDAP","gene_name":"keratinocyte differentiation associated protein [Source:HGNC Symbol;Acc:HGNC:16313]","synonyms":"UNQ467,KDAP","biotype":"protein_coding","ncbi_id":"388533","summary":"This gene encodes a protein which may function in the regulation of keratinocyte differentiation and maintenance of stratified epithelia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":35487324,"end":35495558,"strand":-1,"description":"keratinocyte differentiation associated protein [Source:HGNC Symbol;Acc:HGNC:16313]"}, {"versioned_ensembl_gene_id":"ENSG00000187678.8","gene_symbol":"SPRY4","gene_name":"sprouty RTK signaling antagonist 4 [Source:HGNC Symbol;Acc:HGNC:15533]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81848","summary":"This gene encodes a member of a family of cysteine- and proline-rich proteins. The encoded protein is an inhibitor of the receptor-transduced mitogen-activated protein kinase (MAPK) signaling pathway. Activity of this protein impairs the formation of active GTP-RAS. Nucleotide variation in this gene has been associated with hypogonadotropic hypogonadism 17 with or without anosmia. Alternative splicing results in a multiple transcript variants. [provided by RefSeq, Jun 2014]","start":142310427,"end":142326455,"strand":-1,"description":"sprouty RTK signaling antagonist 4 [Source:HGNC Symbol;Acc:HGNC:15533]"}, {"versioned_ensembl_gene_id":"ENSG00000225951.1","gene_symbol":"ODF2-AS1","gene_name":"ODF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49461]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107080620","summary":null,"start":128468957,"end":128473012,"strand":-1,"description":"ODF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49461]"}, {"versioned_ensembl_gene_id":"ENSG00000262585.1","gene_symbol":"LINC01979","gene_name":"long intergenic non-protein coding RNA 1979 [Source:HGNC Symbol;Acc:HGNC:52807]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928766","summary":null,"start":79915252,"end":79926725,"strand":-1,"description":"long intergenic non-protein coding RNA 1979 [Source:HGNC Symbol;Acc:HGNC:52807]"}, {"versioned_ensembl_gene_id":"ENSG00000267582.1","gene_symbol":"AC020916.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13796574,"end":13796933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141582.14","gene_symbol":"CBX4","gene_name":"chromobox 4 [Source:HGNC Symbol;Acc:HGNC:1554]","synonyms":"PC2,NBP16,hPC2","biotype":"protein_coding","ncbi_id":"8535","summary":null,"start":79833156,"end":79839429,"strand":-1,"description":"chromobox 4 [Source:HGNC Symbol;Acc:HGNC:1554]"}, {"versioned_ensembl_gene_id":"ENSG00000233214.1","gene_symbol":"AC002511.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35424062,"end":35424652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240371.1","gene_symbol":"RPS4XP13","gene_name":"ribosomal protein S4X pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36522]","synonyms":"RPS4P13","biotype":"processed_pseudogene","ncbi_id":"390183","summary":null,"start":57576292,"end":57577080,"strand":-1,"description":"ribosomal protein S4X pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36522]"}, {"versioned_ensembl_gene_id":"ENSG00000267719.1","gene_symbol":"LINC02078","gene_name":"long intergenic non-protein coding RNA 2078 [Source:HGNC Symbol;Acc:HGNC:52926]","synonyms":"HP09025","biotype":"lincRNA","ncbi_id":"100652929","summary":null,"start":79707266,"end":79712317,"strand":1,"description":"long intergenic non-protein coding RNA 2078 [Source:HGNC Symbol;Acc:HGNC:52926]"}, {"versioned_ensembl_gene_id":"ENSG00000187796.14","gene_symbol":"CARD9","gene_name":"caspase recruitment domain family member 9 [Source:HGNC Symbol;Acc:HGNC:16391]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64170","summary":"The protein encoded by this gene is a member of the CARD protein family, which is defined by the presence of a characteristic caspase-associated recruitment domain (CARD). CARD is a protein interaction domain known to participate in activation or suppression of CARD containing members of the caspase family, and thus plays an important regulatory role in cell apoptosis. This protein was identified by its selective association with the CARD domain of BCL10, a postive regulator of apoptosis and NF-kappaB activation, and is thought to function as a molecular scaffold for the assembly of a BCL10 signaling complex that activates NF-kappaB. Several alternatively spliced transcript variants have been observed, but their full-length nature is not clearly defined. [provided by RefSeq, Jul 2008]","start":136361903,"end":136373681,"strand":-1,"description":"caspase recruitment domain family member 9 [Source:HGNC Symbol;Acc:HGNC:16391]"}, {"versioned_ensembl_gene_id":"ENSG00000213221.4","gene_symbol":"DNLZ","gene_name":"DNL-type zinc finger [Source:HGNC Symbol;Acc:HGNC:33879]","synonyms":"ZIM17,TIMM15,RP11-413M3.2,HEP,C9orf151,bA413M3.2","biotype":"protein_coding","ncbi_id":"728489","summary":null,"start":136359480,"end":136363789,"strand":-1,"description":"DNL-type zinc finger [Source:HGNC Symbol;Acc:HGNC:33879]"}, {"versioned_ensembl_gene_id":"ENSG00000271025.1","gene_symbol":"AP000907.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112036627,"end":112036863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259205.2","gene_symbol":"PRKXP1","gene_name":"protein kinase, X-linked, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441733","summary":null,"start":100553529,"end":100558954,"strand":-1,"description":"protein kinase, X-linked, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9442]"}, {"versioned_ensembl_gene_id":"ENSG00000064886.13","gene_symbol":"CHI3L2","gene_name":"chitinase 3 like 2 [Source:HGNC Symbol;Acc:HGNC:1933]","synonyms":"YKL39,YKL-39","biotype":"protein_coding","ncbi_id":"1117","summary":"The protein encoded by this gene is similar to bacterial chitinases but lacks chitinase activity. The encoded protein is secreted and is involved in cartilage biogenesis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":111200771,"end":111243440,"strand":1,"description":"chitinase 3 like 2 [Source:HGNC Symbol;Acc:HGNC:1933]"}, {"versioned_ensembl_gene_id":"ENSG00000270127.2","gene_symbol":"AC027020.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100547765,"end":100550153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229288.1","gene_symbol":"AL451142.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88187735,"end":88190202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226327.3","gene_symbol":"RPSAP49","gene_name":"ribosomal protein SA pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401537","summary":null,"start":88324454,"end":88325339,"strand":1,"description":"ribosomal protein SA pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35660]"}, {"versioned_ensembl_gene_id":"ENSG00000261514.1","gene_symbol":"LINC01976","gene_name":"long intergenic non-protein coding RNA 1976 [Source:HGNC Symbol;Acc:HGNC:52803]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107546764","summary":null,"start":43938363,"end":43938959,"strand":1,"description":"long intergenic non-protein coding RNA 1976 [Source:HGNC Symbol;Acc:HGNC:52803]"}, {"versioned_ensembl_gene_id":"ENSG00000237743.3","gene_symbol":"FBP2P1","gene_name":"fructose-1,6-bisphosphatase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49924]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100420269","summary":null,"start":87810642,"end":87837225,"strand":-1,"description":"fructose-1,6-bisphosphatase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49924]"}, {"versioned_ensembl_gene_id":"ENSG00000283367.1","gene_symbol":"Clostridiales-1","gene_name":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":91356755,"end":91356914,"strand":1,"description":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]"}, {"versioned_ensembl_gene_id":"ENSG00000153827.13","gene_symbol":"TRIP12","gene_name":"thyroid hormone receptor interactor 12 [Source:HGNC Symbol;Acc:HGNC:12306]","synonyms":"KIAA0045","biotype":"protein_coding","ncbi_id":"9320","summary":"The protein encoded by this gene is an E3 ubiquitin-protein ligase involved in the degradation of the p19ARF/ARF isoform of CDKN2A, a tumor suppressor. The encoded protein also plays a role in the DNA damage response by regulating the stability of USP7, which regulates tumor suppressor p53. [provided by RefSeq, Jan 2017]","start":229763838,"end":229923239,"strand":-1,"description":"thyroid hormone receptor interactor 12 [Source:HGNC Symbol;Acc:HGNC:12306]"}, {"versioned_ensembl_gene_id":"ENSG00000148411.7","gene_symbol":"NACC2","gene_name":"NACC family member 2 [Source:HGNC Symbol;Acc:HGNC:23846]","synonyms":"MGC23427,BTBD31,BTBD14A,BEND9","biotype":"protein_coding","ncbi_id":"138151","summary":null,"start":136006537,"end":136095285,"strand":-1,"description":"NACC family member 2 [Source:HGNC Symbol;Acc:HGNC:23846]"}, {"versioned_ensembl_gene_id":"ENSG00000105618.13","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31,PRP31,hPrp31,hPrp31,RP11","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115410,"end":54131719,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000236049.1","gene_symbol":"LINC01920","gene_name":"long intergenic non-protein coding RNA 1920 [Source:HGNC Symbol;Acc:HGNC:52738]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929260","summary":null,"start":150552532,"end":150572221,"strand":-1,"description":"long intergenic non-protein coding RNA 1920 [Source:HGNC Symbol;Acc:HGNC:52738]"}, {"versioned_ensembl_gene_id":"ENSG00000261583.1","gene_symbol":"AC012317.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23711990,"end":23712793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225924.2","gene_symbol":"TAB2-AS1","gene_name":"TAB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53508]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378049","summary":null,"start":149243299,"end":149257551,"strand":-1,"description":"TAB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53508]"}, {"versioned_ensembl_gene_id":"ENSG00000185352.8","gene_symbol":"HS6ST3","gene_name":"heparan sulfate 6-O-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:19134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"266722","summary":"Heparan sulfate (HS) sulfotransferases, such as HS6ST3, modify HS to generate structures required for interactions between HS and a variety of proteins. These interactions are implicated in proliferation and differentiation, adhesion, migration, inflammation, blood coagulation, and other diverse processes (Habuchi et al., 2000 [PubMed 10644753]).[supplied by OMIM, Mar 2008]","start":96090839,"end":96839562,"strand":1,"description":"heparan sulfate 6-O-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:19134]"}, {"versioned_ensembl_gene_id":"ENSG00000228408.6","gene_symbol":"AL031056.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149217926,"end":149245554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283608.1","gene_symbol":"AL031056.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149246095,"end":149255415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279118.1","gene_symbol":"AC093535.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126496279,"end":126498604,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245275.7","gene_symbol":"SAP30L-AS1","gene_name":"SAP30L antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26760]","synonyms":"GALNT10-AS1,FLJ38109","biotype":"antisense_RNA","ncbi_id":"386627","summary":null,"start":154329437,"end":154445850,"strand":-1,"description":"SAP30L antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26760]"}, {"versioned_ensembl_gene_id":"ENSG00000255479.1","gene_symbol":"AP001189.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76625462,"end":76626834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175221.14","gene_symbol":"MED16","gene_name":"mediator complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:17556]","synonyms":"THRAP5,DRIP92,TRAP95","biotype":"protein_coding","ncbi_id":"10025","summary":null,"start":867630,"end":893218,"strand":-1,"description":"mediator complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:17556]"}, {"versioned_ensembl_gene_id":"ENSG00000250579.1","gene_symbol":"AC022424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5132780,"end":5140054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254755.1","gene_symbol":"AP001189.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76591023,"end":76591211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179335.18","gene_symbol":"CLK3","gene_name":"CDC like kinase 3 [Source:HGNC Symbol;Acc:HGNC:2071]","synonyms":"clk3","biotype":"protein_coding","ncbi_id":"1198","summary":"This gene encodes a protein belonging to the serine/threonine type protein kinase family. This protein is a nuclear dual-specificity kinase that regulates the intranuclear distribution of the serine/arginine-rich (SR) family of splicing factors. Two transcript variants encoding different isoforms have been found for this gene. Related pseudogenes are located on chromosomes 1 and 9. [provided by RefSeq, Jul 2008]","start":74598500,"end":74645414,"strand":1,"description":"CDC like kinase 3 [Source:HGNC Symbol;Acc:HGNC:2071]"}, {"versioned_ensembl_gene_id":"ENSG00000238137.2","gene_symbol":"ARPC3P2","gene_name":"actin related protein 2/3 complex subunit 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39431]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391160","summary":null,"start":211442274,"end":211442806,"strand":1,"description":"actin related protein 2/3 complex subunit 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39431]"}, {"versioned_ensembl_gene_id":"ENSG00000234861.2","gene_symbol":"ATP5A1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:827]","synonyms":"ATP5A1P5,ATP5AP1,ATP5AL1,ATP5A1P6","biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42410830,"end":42412150,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:827]"}, {"versioned_ensembl_gene_id":"ENSG00000226686.7","gene_symbol":"LINC01535","gene_name":"long intergenic non-protein coding RNA 1535 [Source:HGNC Symbol;Acc:HGNC:51282]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927667","summary":null,"start":37251912,"end":37265535,"strand":1,"description":"long intergenic non-protein coding RNA 1535 [Source:HGNC Symbol;Acc:HGNC:51282]"}, {"versioned_ensembl_gene_id":"ENSG00000270166.1","gene_symbol":"AL390838.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84078584,"end":84078857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080839.11","gene_symbol":"RBL1","gene_name":"RB transcriptional corepressor like 1 [Source:HGNC Symbol;Acc:HGNC:9893]","synonyms":"PRB1,p107,cp107","biotype":"protein_coding","ncbi_id":"5933","summary":"The protein encoded by this gene is similar in sequence and possibly function to the product of the retinoblastoma 1 (RB1) gene. The RB1 gene product is a tumor suppressor protein that appears to be involved in cell cycle regulation, as it is phosphorylated in the S to M phase transition and is dephosphorylated in the G1 phase of the cell cycle. Both the RB1 protein and the product of this gene can form a complex with adenovirus E1A protein and SV40 large T-antigen, with the SV40 large T-antigen binding only to the unphosphorylated form of each protein. In addition, both proteins can inhibit the transcription of cell cycle genes containing E2F binding sites in their promoters. Due to the sequence and biochemical similarities with the RB1 protein, it is thought that the protein encoded by this gene may also be a tumor suppressor. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":36996349,"end":37095995,"strand":-1,"description":"RB transcriptional corepressor like 1 [Source:HGNC Symbol;Acc:HGNC:9893]"}, {"versioned_ensembl_gene_id":"ENSG00000186493.11","gene_symbol":"C5orf38","gene_name":"chromosome 5 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:24226]","synonyms":"IRX2NB,CEI","biotype":"protein_coding","ncbi_id":"153571","summary":null,"start":2752131,"end":2755397,"strand":1,"description":"chromosome 5 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:24226]"}, {"versioned_ensembl_gene_id":"ENSG00000005075.15","gene_symbol":"POLR2J","gene_name":"RNA polymerase II subunit J [Source:HGNC Symbol;Acc:HGNC:9197]","synonyms":"RPB11m,RPB11A,RPB11,POLR2J1,hRPB14","biotype":"protein_coding","ncbi_id":"5439","summary":"This gene encodes a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene exists as a heterodimer with another polymerase subunit; together they form a core subassembly unit of the polymerase. Two similar genes are located nearby on chromosome 7q22.1 and a pseudogene is found on chromosome 7p13. [provided by RefSeq, Jul 2008]","start":102473118,"end":102478907,"strand":-1,"description":"RNA polymerase II subunit J [Source:HGNC Symbol;Acc:HGNC:9197]"}, {"versioned_ensembl_gene_id":"ENSG00000265964.1","gene_symbol":"AC217774.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45733353,"end":45734669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279685.2","gene_symbol":"MAPT-IT1","gene_name":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100130148","summary":null,"start":45895783,"end":45898798,"strand":1,"description":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]"}, {"versioned_ensembl_gene_id":"ENSG00000239986.2","gene_symbol":"AL445584.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42196333,"end":42196662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276703.1","gene_symbol":"RPS29P32","gene_name":"ribosomal protein S29 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52365]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729158","summary":null,"start":134211450,"end":134211527,"strand":1,"description":"ribosomal protein S29 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52365]"}, {"versioned_ensembl_gene_id":"ENSG00000244471.5","gene_symbol":"AL137058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52488993,"end":52499305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251450.1","gene_symbol":"RASGRF2-AS1","gene_name":"RASGRF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40499]","synonyms":"CTC-459I6.1","biotype":"antisense_RNA","ncbi_id":"102524628","summary":null,"start":80947697,"end":80960907,"strand":-1,"description":"RASGRF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40499]"}, {"versioned_ensembl_gene_id":"ENSG00000249772.1","gene_symbol":"AC026427.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81113385,"end":81114852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224250.1","gene_symbol":"AC025947.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121736303,"end":121739730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223540.1","gene_symbol":"RPS15AP5","gene_name":"ribosomal protein S15a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23743]","synonyms":"Em:AC025947.3","biotype":"processed_pseudogene","ncbi_id":"414230","summary":null,"start":121713607,"end":121713994,"strand":1,"description":"ribosomal protein S15a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23743]"}, {"versioned_ensembl_gene_id":"ENSG00000259789.1","gene_symbol":"AL096869.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90489012,"end":90491637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181705.2","gene_symbol":"AL596028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80499196,"end":80499392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259757.1","gene_symbol":"AC091891.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2736662,"end":2737759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280022.1","gene_symbol":"AC126544.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45592621,"end":45593369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263503.1","gene_symbol":"MAPK8IP1P2","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52402]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644172","summary":null,"start":45600869,"end":45602340,"strand":-1,"description":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52402]"}, {"versioned_ensembl_gene_id":"ENSG00000276809.1","gene_symbol":"AL138955.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":95744726,"end":95745765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102580.14","gene_symbol":"DNAJC3","gene_name":"DnaJ heat shock protein family (Hsp40) member C3 [Source:HGNC Symbol;Acc:HGNC:9439]","synonyms":"PRKRI,P58IPK,P58,HP58,ERdj6","biotype":"protein_coding","ncbi_id":"5611","summary":"This gene encodes a protein with multiple tetratricopeptide repeat (TPR) motifs as well as the highly conserved J domain found in DNAJ chaperone family members. It is a member of the tetratricopeptide repeat family of proteins and acts as an inhibitor of the interferon-induced, dsRNA-activated protein kinase (PKR). [provided by RefSeq, Jul 2010]","start":95677139,"end":95794989,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C3 [Source:HGNC Symbol;Acc:HGNC:9439]"}, {"versioned_ensembl_gene_id":"ENSG00000163915.7","gene_symbol":"IGF2BP2-AS1","gene_name":"IGF2BP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32674]","synonyms":"FLJ32900,C3orf65","biotype":"antisense_RNA","ncbi_id":"646600","summary":null,"start":185712528,"end":185729787,"strand":1,"description":"IGF2BP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32674]"}, {"versioned_ensembl_gene_id":"ENSG00000229369.1","gene_symbol":"AL450263.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127300093,"end":127300982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172890.11","gene_symbol":"NADSYN1","gene_name":"NAD synthetase 1 [Source:HGNC Symbol;Acc:HGNC:29832]","synonyms":"FLJ10631","biotype":"protein_coding","ncbi_id":"55191","summary":"Nicotinamide adenine dinucleotide (NAD) is a coenzyme in metabolic redox reactions, a precursor for several cell signaling molecules, and a substrate for protein posttranslational modifications. NAD synthetase (EC 6.3.5.1) catalyzes the final step in the biosynthesis of NAD from nicotinic acid adenine dinucleotide (NaAD).[supplied by OMIM, Apr 2004]","start":71453109,"end":71524107,"strand":1,"description":"NAD synthetase 1 [Source:HGNC Symbol;Acc:HGNC:29832]"}, {"versioned_ensembl_gene_id":"ENSG00000187550.8","gene_symbol":"SBK2","gene_name":"SH3 domain binding kinase family member 2 [Source:HGNC Symbol;Acc:HGNC:34416]","synonyms":"SGK069","biotype":"protein_coding","ncbi_id":"646643","summary":null,"start":55529733,"end":55537089,"strand":-1,"description":"SH3 domain binding kinase family member 2 [Source:HGNC Symbol;Acc:HGNC:34416]"}, {"versioned_ensembl_gene_id":"ENSG00000258788.3","gene_symbol":"CKS1BP1","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20004]","synonyms":"CKS1BP","biotype":"processed_pseudogene","ncbi_id":"317780","summary":null,"start":96223108,"end":96223347,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20004]"}, {"versioned_ensembl_gene_id":"ENSG00000179954.15","gene_symbol":"SSC5D","gene_name":"scavenger receptor cysteine rich family member with 5 domains [Source:HGNC Symbol;Acc:HGNC:26641]","synonyms":"S5D-SRCRB,FLJ35258","biotype":"protein_coding","ncbi_id":"284297","summary":null,"start":55488404,"end":55519098,"strand":1,"description":"scavenger receptor cysteine rich family member with 5 domains [Source:HGNC Symbol;Acc:HGNC:26641]"}, {"versioned_ensembl_gene_id":"ENSG00000100721.10","gene_symbol":"TCL1A","gene_name":"T-cell leukemia/lymphoma 1A [Source:HGNC Symbol;Acc:HGNC:11648]","synonyms":"TCL1","biotype":"protein_coding","ncbi_id":"8115","summary":"Overexpression of the TCL1 gene in humans has been implicated in the development of mature T cell leukemia, in which chromosomal rearrangements bring the TCL1 gene in close proximity to the T-cell antigen receptor (TCR)-alpha (MIM 186880) or TCR-beta (MIM 186930) regulatory elements (summarized by Virgilio et al., 1998 [PubMed 9520462]). In normal T cells TCL1 is expressed in CD4-/CD8- cells, but not in cells at later stages of differentiation. TCL1 functions as a coactivator of the cell survival kinase AKT (MIM 164730) (Laine et al., 2000 [PubMed 10983986]).[supplied by OMIM, Jul 2010]","start":95709967,"end":95714196,"strand":-1,"description":"T-cell leukemia/lymphoma 1A [Source:HGNC Symbol;Acc:HGNC:11648]"}, {"versioned_ensembl_gene_id":"ENSG00000161547.16","gene_symbol":"SRSF2","gene_name":"serine and arginine rich splicing factor 2 [Source:HGNC Symbol;Acc:HGNC:10783]","synonyms":"SC-35,PR264,SFRS2A,SFRS2,SC35","biotype":"protein_coding","ncbi_id":"6427","summary":"The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two transcript variants encoding the same protein and one non-coding transcript variant have been found for this gene. In addition, a pseudogene of this gene has been found on chromosome 11. [provided by RefSeq, Sep 2010]","start":76734115,"end":76737374,"strand":-1,"description":"serine and arginine rich splicing factor 2 [Source:HGNC Symbol;Acc:HGNC:10783]"}, {"versioned_ensembl_gene_id":"ENSG00000076706.16","gene_symbol":"MCAM","gene_name":"melanoma cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:6934]","synonyms":"MUC18,CD146","biotype":"protein_coding","ncbi_id":"4162","summary":null,"start":119308529,"end":119321521,"strand":-1,"description":"melanoma cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:6934]"}, {"versioned_ensembl_gene_id":"ENSG00000164176.12","gene_symbol":"EDIL3","gene_name":"EGF like repeats and discoidin domains 3 [Source:HGNC Symbol;Acc:HGNC:3173]","synonyms":"DEL1","biotype":"protein_coding","ncbi_id":"10085","summary":"The protein encoded by this gene is an integrin ligand. It plays an important role in mediating angiogenesis and may be important in vessel wall remodeling and development. It also influences endothelial cell behavior. [provided by RefSeq, Jul 2008]","start":83940554,"end":84384793,"strand":-1,"description":"EGF like repeats and discoidin domains 3 [Source:HGNC Symbol;Acc:HGNC:3173]"}, {"versioned_ensembl_gene_id":"ENSG00000249904.1","gene_symbol":"AC010587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125886285,"end":125886753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063854.12","gene_symbol":"HAGH","gene_name":"hydroxyacylglutathione hydrolase [Source:HGNC Symbol;Acc:HGNC:4805]","synonyms":"HAGH1,GLXII,GLO2","biotype":"protein_coding","ncbi_id":"3029","summary":"The enzyme encoded by this gene is classified as a thiolesterase and is responsible for the hydrolysis of S-lactoyl-glutathione to reduced glutathione and D-lactate. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":1795620,"end":1827194,"strand":-1,"description":"hydroxyacylglutathione hydrolase [Source:HGNC Symbol;Acc:HGNC:4805]"}, {"versioned_ensembl_gene_id":"ENSG00000189420.8","gene_symbol":"ZFP92","gene_name":"ZFP92 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12865]","synonyms":"ZNF897","biotype":"protein_coding","ncbi_id":"139735","summary":null,"start":153418322,"end":153426481,"strand":1,"description":"ZFP92 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12865]"}, {"versioned_ensembl_gene_id":"ENSG00000219928.2","gene_symbol":"AL161787.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87525302,"end":87525475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281608.1","gene_symbol":"AC109471.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125325350,"end":125367734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280163.1","gene_symbol":"AC040160.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67205175,"end":67206849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250641.1","gene_symbol":"AL662899.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31706904,"end":31717918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180787.5","gene_symbol":"ZFP3","gene_name":"ZFP3 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12861]","synonyms":"ZNF752,FLJ30726","biotype":"protein_coding","ncbi_id":"124961","summary":null,"start":5078248,"end":5096374,"strand":1,"description":"ZFP3 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:12861]"}, {"versioned_ensembl_gene_id":"ENSG00000204424.9","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"G6f,NG32,C6orf21,LY6G6D","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31706885,"end":31710595,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000238150.1","gene_symbol":"AC008753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53775599,"end":53775882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253703.2","gene_symbol":"IGHV1-68","gene_name":"immunoglobulin heavy variable 1-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5557]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28462","summary":null,"start":106703846,"end":106704286,"strand":-1,"description":"immunoglobulin heavy variable 1-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5557]"}, {"versioned_ensembl_gene_id":"ENSG00000265698.1","gene_symbol":"LARP7P3","gene_name":"La ribonucleoprotein domain family member 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481700","summary":null,"start":70412055,"end":70412391,"strand":1,"description":"La ribonucleoprotein domain family member 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49765]"}, {"versioned_ensembl_gene_id":"ENSG00000160856.20","gene_symbol":"FCRL3","gene_name":"Fc receptor like 3 [Source:HGNC Symbol;Acc:HGNC:18506]","synonyms":"IFGP3,FCRH3,CD307c,SPAP2e,SPAP2d,SPAP2c,SPAP2b,SPAP2a,SPAP2,IRTA3","biotype":"protein_coding","ncbi_id":"115352","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains immunoreceptor-tyrosine activation motifs and immunoreceptor-tyrosine inhibitory motifs in its cytoplasmic domain and may play a role in regulation of the immune system. Mutations in this gene have been associated with rheumatoid arthritis, autoimmune thyroid disease, and systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":157674321,"end":157700857,"strand":-1,"description":"Fc receptor like 3 [Source:HGNC Symbol;Acc:HGNC:18506]"}, {"versioned_ensembl_gene_id":"ENSG00000101282.8","gene_symbol":"RSPO4","gene_name":"R-spondin 4 [Source:HGNC Symbol;Acc:HGNC:16175]","synonyms":"dJ824F16.3,C20orf182","biotype":"protein_coding","ncbi_id":"343637","summary":"This gene encodes a member of the R-spondin family of proteins that share a common domain organization consisting of a signal peptide, cysteine-rich/furin-like domain, thrombospondin domain and a C-terminal basic region. The encoded protein may be involved in activation of Wnt/beta-catenin signaling pathways. Mutations in this gene are associated with anonychia congenital. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]","start":958452,"end":1002264,"strand":-1,"description":"R-spondin 4 [Source:HGNC Symbol;Acc:HGNC:16175]"}, {"versioned_ensembl_gene_id":"ENSG00000213231.12","gene_symbol":"TCL1B","gene_name":"T-cell leukemia/lymphoma 1B [Source:HGNC Symbol;Acc:HGNC:11649]","synonyms":"TML1","biotype":"protein_coding","ncbi_id":"9623","summary":null,"start":95686417,"end":95692643,"strand":1,"description":"T-cell leukemia/lymphoma 1B [Source:HGNC Symbol;Acc:HGNC:11649]"}, {"versioned_ensembl_gene_id":"ENSG00000183032.11","gene_symbol":"SLC25A21","gene_name":"solute carrier family 25 member 21 [Source:HGNC Symbol;Acc:HGNC:14411]","synonyms":"ODC1,ODC","biotype":"protein_coding","ncbi_id":"89874","summary":"SLC25A21 is a homolog of the S. cerevisiae ODC proteins, mitochondrial carriers that transport C5-C7 oxodicarboxylates across inner mitochondrial membranes. One of the species transported by ODC is 2-oxoadipate, a common intermediate in the catabolism of lysine, tryptophan, and hydroxylysine in mammals. Within mitochondria, 2-oxoadipate is converted into acetyl-CoA.[supplied by OMIM, Apr 2004]","start":36678431,"end":37172866,"strand":-1,"description":"solute carrier family 25 member 21 [Source:HGNC Symbol;Acc:HGNC:14411]"}, {"versioned_ensembl_gene_id":"ENSG00000225396.5","gene_symbol":"FAM236D","gene_name":"family with sequence similarity 236 member D [Source:HGNC Symbol;Acc:HGNC:52642]","synonyms":null,"biotype":"protein_coding","ncbi_id":"105373251","summary":null,"start":72807425,"end":72808210,"strand":-1,"description":"family with sequence similarity 236 member D [Source:HGNC Symbol;Acc:HGNC:52642]"}, {"versioned_ensembl_gene_id":"ENSG00000136352.17","gene_symbol":"NKX2-1","gene_name":"NK2 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11825]","synonyms":"TTF1,TTF-1,TITF1,NKX2A,BCH","biotype":"protein_coding","ncbi_id":"7080","summary":"This gene encodes a protein initially identified as a thyroid-specific transcription factor. The encoded protein binds to the thyroglobulin promoter and regulates the expression of thyroid-specific genes but has also been shown to regulate the expression of genes involved in morphogenesis. Mutations and deletions in this gene are associated with benign hereditary chorea, choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress, and may be associated with thyroid cancer. Multiple transcript variants encoding different isoforms have been found for this gene. This gene shares the symbol/alias 'TTF1' with another gene, transcription termination factor 1, which plays a role in ribosomal gene transcription. [provided by RefSeq, Feb 2014]","start":36516392,"end":36521149,"strand":-1,"description":"NK2 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11825]"}, {"versioned_ensembl_gene_id":"ENSG00000267706.3","gene_symbol":"AC020922.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55352301,"end":55359516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244207.8","gene_symbol":"C4A","gene_name":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]","synonyms":"CPAMD2,C4A2,C4A6,CO4,C4,C4A4,C4S,RG,C4A3,C4B","biotype":"protein_coding","ncbi_id":"720","summary":"This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain is cleaved to release C4 anaphylatoxin, an antimicrobial peptide and a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":31964204,"end":31984862,"strand":1,"description":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]"}, {"versioned_ensembl_gene_id":"ENSG00000248712.7","gene_symbol":"CCDC153","gene_name":"coiled-coil domain containing 153 [Source:HGNC Symbol;Acc:HGNC:27446]","synonyms":"LOC283152","biotype":"protein_coding","ncbi_id":"283152","summary":null,"start":119189638,"end":119196769,"strand":-1,"description":"coiled-coil domain containing 153 [Source:HGNC Symbol;Acc:HGNC:27446]"}, {"versioned_ensembl_gene_id":"ENSG00000174780.15","gene_symbol":"SRP72","gene_name":"signal recognition particle 72 [Source:HGNC Symbol;Acc:HGNC:11303]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6731","summary":"This gene encodes the 72 kDa subunit of the signal recognition particle (SRP), a ribonucleoprotein complex that mediates the targeting of secretory proteins to the endoplasmic reticulum (ER). The SRP complex consists of a 7S RNA and 6 protein subunits: SRP9, SRP14, SRP19, SRP54, SRP68, and SRP72, that are bound to the 7S RNA as monomers or heterodimers. SRP has at least 3 distinct functions that can be associated with the protein subunits: signal recognition, translational arrest, and ER membrane targeting by interaction with the docking protein. Mutations in this gene are associated with familial bone marrow failure. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":56466915,"end":56503680,"strand":1,"description":"signal recognition particle 72 [Source:HGNC Symbol;Acc:HGNC:11303]"}, {"versioned_ensembl_gene_id":"ENSG00000256632.3","gene_symbol":"AC135586.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":132688049,"end":132714912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228757.1","gene_symbol":"AC244452.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106436415,"end":106436555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254594.5","gene_symbol":"AC015771.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24235477,"end":24262218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253467.2","gene_symbol":"IGHV7-40","gene_name":"immunoglobulin heavy variable 7-40 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5666]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28381","summary":null,"start":106425359,"end":106425654,"strand":-1,"description":"immunoglobulin heavy variable 7-40 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5666]"}, {"versioned_ensembl_gene_id":"ENSG00000142319.17","gene_symbol":"SLC6A3","gene_name":"solute carrier family 6 member 3 [Source:HGNC Symbol;Acc:HGNC:11049]","synonyms":"DAT1,DAT","biotype":"protein_coding","ncbi_id":"6531","summary":"This gene encodes a dopamine transporter which is a member of the sodium- and chloride-dependent neurotransmitter transporter family. The 3' UTR of this gene contains a 40 bp tandem repeat, referred to as a variable number tandem repeat or VNTR, which can be present in 3 to 11 copies. Variation in the number of repeats is associated with idiopathic epilepsy, attention-deficit hyperactivity disorder, dependence on alcohol and cocaine, susceptibility to Parkinson disease and protection against nicotine dependence.[provided by RefSeq, Nov 2009]","start":1392790,"end":1445430,"strand":-1,"description":"solute carrier family 6 member 3 [Source:HGNC Symbol;Acc:HGNC:11049]"}, {"versioned_ensembl_gene_id":"ENSG00000049656.13","gene_symbol":"CLPTM1L","gene_name":"CLPTM1 like [Source:HGNC Symbol;Acc:HGNC:24308]","synonyms":"FLJ14400,CRR9","biotype":"protein_coding","ncbi_id":"81037","summary":"The protein encoded by this gene is a membrane protein whose overexpression in cisplatin-sensitive cells causes apoptosis. Polymorphisms in this gene have been reported to increase susceptibility to several cancers, including lung, pancreatic, and breast cancers. [provided by RefSeq, Nov 2015]","start":1317744,"end":1345099,"strand":-1,"description":"CLPTM1 like [Source:HGNC Symbol;Acc:HGNC:24308]"}, {"versioned_ensembl_gene_id":"ENSG00000067177.14","gene_symbol":"PHKA1","gene_name":"phosphorylase kinase regulatory subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:8925]","synonyms":"PHKA","biotype":"protein_coding","ncbi_id":"5255","summary":"Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, and the skeletal muscle isoform is encoded by this gene. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, which are encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9D, also known as X-linked muscle glycogenosis. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. A pseudogene has been found on chromosome 1.[provided by RefSeq, Feb 2010]","start":72578814,"end":72714319,"strand":-1,"description":"phosphorylase kinase regulatory subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:8925]"}, {"versioned_ensembl_gene_id":"ENSG00000240881.1","gene_symbol":"AC068472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23520322,"end":23521202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255475.1","gene_symbol":"AP001007.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125132847,"end":125139587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254351.1","gene_symbol":"ARL2BPP5","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39449]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874420","summary":null,"start":162761833,"end":162762313,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39449]"}, {"versioned_ensembl_gene_id":"ENSG00000242618.1","gene_symbol":"AC112219.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72202944,"end":72209892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232791.3","gene_symbol":"OR11I1P","gene_name":"olfactory receptor family 11 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14997]","synonyms":"OR11I2P","biotype":"unitary_pseudogene","ncbi_id":"81479","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":110853938,"end":110854891,"strand":1,"description":"olfactory receptor family 11 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14997]"}, {"versioned_ensembl_gene_id":"ENSG00000254465.1","gene_symbol":"THAP12P4","gene_name":"THAP domain containing 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39568]","synonyms":"PRKRIRP4","biotype":"processed_pseudogene","ncbi_id":"100129382","summary":null,"start":23478068,"end":23480430,"strand":1,"description":"THAP domain containing 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39568]"}, {"versioned_ensembl_gene_id":"ENSG00000237924.1","gene_symbol":"RPL21P112","gene_name":"ribosomal protein L21 pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:36526]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270753","summary":null,"start":94760553,"end":94761015,"strand":-1,"description":"ribosomal protein L21 pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:36526]"}, {"versioned_ensembl_gene_id":"ENSG00000254564.1","gene_symbol":"AC100767.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23431677,"end":23431799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232455.2","gene_symbol":"LARS2-AS1","gene_name":"LARS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40796]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885795","summary":null,"start":45483974,"end":45509545,"strand":-1,"description":"LARS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40796]"}, {"versioned_ensembl_gene_id":"ENSG00000248773.1","gene_symbol":"AC108727.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":140972744,"end":140973255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186790.5","gene_symbol":"FOXE3","gene_name":"forkhead box E3 [Source:HGNC Symbol;Acc:HGNC:3808]","synonyms":"FREAC8,FKHL12","biotype":"protein_coding","ncbi_id":"2301","summary":"This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia. [provided by RefSeq, Dec 2009]","start":47416072,"end":47418052,"strand":1,"description":"forkhead box E3 [Source:HGNC Symbol;Acc:HGNC:3808]"}, {"versioned_ensembl_gene_id":"ENSG00000271049.1","gene_symbol":"AC020910.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34634844,"end":34635717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163629.12","gene_symbol":"PTPN13","gene_name":"protein tyrosine phosphatase, non-receptor type 13 [Source:HGNC Symbol;Acc:HGNC:9646]","synonyms":"PTPL1,PTP1E,PTP-BL,PTP-BAS","biotype":"protein_coding","ncbi_id":"5783","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP is a large intracellular protein. It has a catalytic PTP domain at its C-terminus and two major structural domains: a region with five PDZ domains and a FERM domain that binds to plasma membrane and cytoskeletal elements. This PTP was found to interact with, and dephosphorylate, Fas receptor and IkappaBalpha through the PDZ domains. This suggests it has a role in Fas mediated programmed cell death. This PTP was also shown to interact with GTPase-activating protein, and thus may function as a regulator of Rho signaling pathways. Four alternatively spliced transcript variants, which encode distinct proteins, have been reported. [provided by RefSeq, Oct 2008]","start":86594315,"end":86815171,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 13 [Source:HGNC Symbol;Acc:HGNC:9646]"}, {"versioned_ensembl_gene_id":"ENSG00000197595.4","gene_symbol":"ATP11AUN","gene_name":"ATP11A upstream neighbor [Source:HGNC Symbol;Acc:HGNC:33793]","synonyms":"SMABLO1,FLJ26443,C13orf35","biotype":"lincRNA","ncbi_id":"400165","summary":null,"start":112647044,"end":112684497,"strand":1,"description":"ATP11A upstream neighbor [Source:HGNC Symbol;Acc:HGNC:33793]"}, {"versioned_ensembl_gene_id":"ENSG00000251377.1","gene_symbol":"AC079340.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152207421,"end":152225870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260287.4","gene_symbol":"TBC1D3G","gene_name":"TBC1 domain family member 3G [Source:HGNC Symbol;Acc:HGNC:29860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060321","summary":null,"start":36323884,"end":36334759,"strand":1,"description":"TBC1 domain family member 3G [Source:HGNC Symbol;Acc:HGNC:29860]"}, {"versioned_ensembl_gene_id":"ENSG00000249961.9","gene_symbol":"TERB1","gene_name":"telomere repeat binding bouquet formation protein 1 [Source:HGNC Symbol;Acc:HGNC:26675]","synonyms":"FLJ35894,CCDC79","biotype":"protein_coding","ncbi_id":"283847","summary":null,"start":66754976,"end":66801620,"strand":-1,"description":"telomere repeat binding bouquet formation protein 1 [Source:HGNC Symbol;Acc:HGNC:26675]"}, {"versioned_ensembl_gene_id":"ENSG00000277940.1","gene_symbol":"AC245128.14","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228392.1","gene_symbol":"AL162391.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126270121,"end":126275918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277851.1","gene_symbol":"LINC02391","gene_name":"long intergenic non-protein coding RNA 2391 [Source:HGNC Symbol;Acc:HGNC:53318]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101930023","summary":null,"start":92247756,"end":92363832,"strand":-1,"description":"long intergenic non-protein coding RNA 2391 [Source:HGNC Symbol;Acc:HGNC:53318]"}, {"versioned_ensembl_gene_id":"ENSG00000205089.7","gene_symbol":"CCNI2","gene_name":"cyclin I family member 2 [Source:HGNC Symbol;Acc:HGNC:33869]","synonyms":"FLJ16793","biotype":"protein_coding","ncbi_id":"645121","summary":null,"start":132747445,"end":132754403,"strand":1,"description":"cyclin I family member 2 [Source:HGNC Symbol;Acc:HGNC:33869]"}, {"versioned_ensembl_gene_id":"ENSG00000261763.1","gene_symbol":"AC110716.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139678620,"end":139682564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250543.1","gene_symbol":"AC110716.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139688403,"end":139689342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211946.3","gene_symbol":"IGHV3-20","gene_name":"immunoglobulin heavy variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5585]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28445","summary":null,"start":106210936,"end":106211453,"strand":-1,"description":"immunoglobulin heavy variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5585]"}, {"versioned_ensembl_gene_id":"ENSG00000253458.1","gene_symbol":"IGHVII-15-1","gene_name":"immunoglobulin heavy variable (II)-15-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5671]","synonyms":"IGHV(II)-15-1","biotype":"IG_V_pseudogene","ncbi_id":"28376","summary":null,"start":106163583,"end":106163802,"strand":-1,"description":"immunoglobulin heavy variable (II)-15-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5671]"}, {"versioned_ensembl_gene_id":"ENSG00000253709.1","gene_symbol":"IGHV1-14","gene_name":"immunoglobulin heavy variable 1-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5547]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28470","summary":null,"start":106145891,"end":106146131,"strand":-1,"description":"immunoglobulin heavy variable 1-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5547]"}, {"versioned_ensembl_gene_id":"ENSG00000112659.13","gene_symbol":"CUL9","gene_name":"cullin 9 [Source:HGNC Symbol;Acc:HGNC:15982]","synonyms":"PARC,KIAA0708,H7AP1","biotype":"protein_coding","ncbi_id":"23113","summary":null,"start":43182175,"end":43224587,"strand":1,"description":"cullin 9 [Source:HGNC Symbol;Acc:HGNC:15982]"}, {"versioned_ensembl_gene_id":"ENSG00000007908.15","gene_symbol":"SELE","gene_name":"selectin E [Source:HGNC Symbol;Acc:HGNC:10718]","synonyms":"CD62E,ESEL,ELAM1,ELAM","biotype":"protein_coding","ncbi_id":"6401","summary":"The protein encoded by this gene is found in cytokine-stimulated endothelial cells and is thought to be responsible for the accumulation of blood leukocytes at sites of inflammation by mediating the adhesion of cells to the vascular lining. It exhibits structural features such as the presence of lectin- and EGF-like domains followed by short consensus repeat (SCR) domains that contain 6 conserved cysteine residues. These proteins are part of the selectin family of cell adhesion molecules. Adhesion molecules participate in the interaction between leukocytes and the endothelium and appear to be involved in the pathogenesis of atherosclerosis. [provided by RefSeq, Jul 2008]","start":169722641,"end":169764705,"strand":-1,"description":"selectin E [Source:HGNC Symbol;Acc:HGNC:10718]"}, {"versioned_ensembl_gene_id":"ENSG00000274808.5","gene_symbol":"TBC1D3B","gene_name":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]","synonyms":"PRC17,TBC1D3I,PRC17,TBC1D3I","biotype":"protein_coding","ncbi_id":"414059","summary":"This gene encodes a protein that is similar to TBC1 domain family, member 3. This protein contains a TBC (Tre-2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q. [provided by RefSeq, Apr 2009]","start":36165681,"end":36176636,"strand":-1,"description":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]"}, {"versioned_ensembl_gene_id":"ENSG00000229499.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29810065,"end":29810196,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000124203.6","gene_symbol":"ZNF831","gene_name":"zinc finger protein 831 [Source:HGNC Symbol;Acc:HGNC:16167]","synonyms":"dJ492J12.1,C20orf174","biotype":"protein_coding","ncbi_id":"128611","summary":null,"start":59123381,"end":59259113,"strand":1,"description":"zinc finger protein 831 [Source:HGNC Symbol;Acc:HGNC:16167]"}, {"versioned_ensembl_gene_id":"ENSG00000236005.1","gene_symbol":"AL389915.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107534390,"end":107535162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239354.1","gene_symbol":"RPS17P15","gene_name":"ribosomal protein S17 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271363","summary":null,"start":111105547,"end":111105895,"strand":-1,"description":"ribosomal protein S17 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35931]"}, {"versioned_ensembl_gene_id":"ENSG00000232543.2","gene_symbol":"IGHD4-11","gene_name":"immunoglobulin heavy diversity 4-11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5502]","synonyms":"IGHD411,DA1","biotype":"IG_D_gene","ncbi_id":"28495","summary":null,"start":105903616,"end":105903631,"strand":-1,"description":"immunoglobulin heavy diversity 4-11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5502]"}, {"versioned_ensembl_gene_id":"ENSG00000135720.12","gene_symbol":"DYNC1LI2","gene_name":"dynein cytoplasmic 1 light intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:2966]","synonyms":"DNCLI2","biotype":"protein_coding","ncbi_id":"1783","summary":"Cytoplasmic dynein is a microtubule-associated motor protein (Hughes et al., 1995 [PubMed 7738094]). See DYNC1H1 (MIM 600112) for general information about dyneins.[supplied by OMIM, Mar 2008]","start":66720893,"end":66751798,"strand":-1,"description":"dynein cytoplasmic 1 light intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:2966]"}, {"versioned_ensembl_gene_id":"ENSG00000280987.4","gene_symbol":"MATR3","gene_name":"matrin 3 [Source:NCBI gene;Acc:9782]","synonyms":"VCPDM,VCPDM,MPD2,MPD2,MGC9105,ALS21,KIAA0723","biotype":"protein_coding","ncbi_id":"9782","summary":"This gene encodes a nuclear matrix protein, which is proposed to stabilize certain messenger RNA species. Mutations of this gene are associated with distal myopathy 2, which often includes vocal cord and pharyngeal weakness. Alternatively spliced transcript variants, including read-through transcripts composed of the upstream small nucleolar RNA host gene 4 (non-protein coding) and matrin 3 gene sequence, have been identified. Pseudogenes of this gene are located on chromosomes 1 and X. [provided by RefSeq, Aug 2013]","start":139273752,"end":139331671,"strand":1,"description":"matrin 3 [Source:NCBI gene;Acc:9782]"}, {"versioned_ensembl_gene_id":"ENSG00000211611.2","gene_symbol":"IGKV6-21","gene_name":"immunoglobulin kappa variable 6-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5836]","synonyms":"IGKV621,A26","biotype":"IG_V_gene","ncbi_id":"28906","summary":null,"start":89159751,"end":89160366,"strand":-1,"description":"immunoglobulin kappa variable 6-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5836]"}, {"versioned_ensembl_gene_id":"ENSG00000237547.1","gene_symbol":"IGHJ2P","gene_name":"immunoglobulin heavy joining 2P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5535]","synonyms":"Jpsi2","biotype":"IG_J_pseudogene","ncbi_id":"28480","summary":null,"start":105864793,"end":105864852,"strand":-1,"description":"immunoglobulin heavy joining 2P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5535]"}, {"versioned_ensembl_gene_id":"ENSG00000242887.1","gene_symbol":"IGHJ3","gene_name":"immunoglobulin heavy joining 3 [Source:HGNC Symbol;Acc:HGNC:5536]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28479","summary":null,"start":105864587,"end":105864635,"strand":-1,"description":"immunoglobulin heavy joining 3 [Source:HGNC Symbol;Acc:HGNC:5536]"}, {"versioned_ensembl_gene_id":"ENSG00000250508.1","gene_symbol":"AP000808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68870664,"end":68874542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121281.12","gene_symbol":"ADCY7","gene_name":"adenylate cyclase 7 [Source:HGNC Symbol;Acc:HGNC:238]","synonyms":"KIAA0037,AC7","biotype":"protein_coding","ncbi_id":"113","summary":"This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. Several transcript variants have been observed for this gene, but the full-length natures of only two have been determined so far. [provided by RefSeq, Oct 2013]","start":50246137,"end":50318135,"strand":1,"description":"adenylate cyclase 7 [Source:HGNC Symbol;Acc:HGNC:238]"}, {"versioned_ensembl_gene_id":"ENSG00000110243.11","gene_symbol":"APOA5","gene_name":"apolipoprotein A5 [Source:HGNC Symbol;Acc:HGNC:17288]","synonyms":"RAP3,APOA-V","biotype":"protein_coding","ncbi_id":"116519","summary":"The protein encoded by this gene is an apolipoprotein that plays an important role in regulating the plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component of high density lipoprotein and is highly similar to a rat protein that is upregulated in response to liver injury. Mutations in this gene have been associated with hypertriglyceridemia and hyperlipoproteinemia type 5. This gene is located proximal to the apolipoprotein gene cluster on chromosome 11q23. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Oct 2009]","start":116789367,"end":116792420,"strand":-1,"description":"apolipoprotein A5 [Source:HGNC Symbol;Acc:HGNC:17288]"}, {"versioned_ensembl_gene_id":"ENSG00000272243.5","gene_symbol":"AL356277.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74530248,"end":74734279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197894.10","gene_symbol":"ADH5","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide [Source:HGNC Symbol;Acc:HGNC:253]","synonyms":"GSNOR,FDH,ADHX,ADH-3","biotype":"protein_coding","ncbi_id":"128","summary":"This gene encodes a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. The encoded protein forms a homodimer. It has virtually no activity for ethanol oxidation, but exhibits high activity for oxidation of long-chain primary alcohols and for oxidation of S-hydroxymethyl-glutathione, a spontaneous adduct between formaldehyde and glutathione. This enzyme is an important component of cellular metabolism for the elimination of formaldehyde, a potent irritant and sensitizing agent that causes lacrymation, rhinitis, pharyngitis, and contact dermatitis. The human genome contains several non-transcribed pseudogenes related to this gene. [provided by RefSeq, Oct 2008]","start":99070978,"end":99088801,"strand":-1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide [Source:HGNC Symbol;Acc:HGNC:253]"}, {"versioned_ensembl_gene_id":"ENSG00000260735.1","gene_symbol":"AC139256.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15094411,"end":15109197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275910.1","gene_symbol":"AC138932.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15015828,"end":15016390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140675.12","gene_symbol":"SLC5A2","gene_name":"solute carrier family 5 member 2 [Source:HGNC Symbol;Acc:HGNC:11037]","synonyms":"SGLT2","biotype":"protein_coding","ncbi_id":"6524","summary":"This gene encodes a member of the sodium glucose cotransporter family which are sodium-dependent glucose transport proteins. The encoded protein is the major cotransporter involved in glucose reabsorption in the kidney. Mutations in this gene are associated with renal glucosuria. Two transcript variants, one protein-coding and one not, have been found for this gene. [provided by RefSeq, Feb 2015]","start":31483002,"end":31490860,"strand":1,"description":"solute carrier family 5 member 2 [Source:HGNC Symbol;Acc:HGNC:11037]"}, {"versioned_ensembl_gene_id":"ENSG00000007038.10","gene_symbol":"PRSS21","gene_name":"protease, serine 21 [Source:HGNC Symbol;Acc:HGNC:9485]","synonyms":"TEST1,ESP-1","biotype":"protein_coding","ncbi_id":"10942","summary":"This gene encodes a cell-surface anchored serine protease, which is a member of the trypsin family of serine proteases. The encoded protein is predicted to be active on peptide linkages involving the carboxyl group of lysine or arginine. The encoded protein localizes to the cytoplasm and the plasma membrane of premeiotic testicular germ cells and may be involved in progression of testicular tumors of germ cell origin. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":2817180,"end":2826304,"strand":1,"description":"protease, serine 21 [Source:HGNC Symbol;Acc:HGNC:9485]"}, {"versioned_ensembl_gene_id":"ENSG00000211896.7","gene_symbol":"IGHG1","gene_name":"immunoglobulin heavy constant gamma 1 (G1m marker) [Source:HGNC Symbol;Acc:HGNC:5525]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3500","summary":null,"start":105736343,"end":105743071,"strand":-1,"description":"immunoglobulin heavy constant gamma 1 (G1m marker) [Source:HGNC Symbol;Acc:HGNC:5525]"}, {"versioned_ensembl_gene_id":"ENSG00000230612.3","gene_symbol":"AC004039.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132688681,"end":132723725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101132.9","gene_symbol":"PFDN4","gene_name":"prefoldin subunit 4 [Source:HGNC Symbol;Acc:HGNC:8868]","synonyms":"PFD4,C1,C-1","biotype":"protein_coding","ncbi_id":"5203","summary":"This gene encodes a member of the prefoldin beta subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. [provided by RefSeq, Jul 2008]","start":54207847,"end":54228052,"strand":1,"description":"prefoldin subunit 4 [Source:HGNC Symbol;Acc:HGNC:8868]"}, {"versioned_ensembl_gene_id":"ENSG00000237002.6","gene_symbol":"AL590730.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36438616,"end":36442392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278169.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54684990,"end":54697367,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000258866.1","gene_symbol":"AL390254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95048220,"end":95050953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224959.1","gene_symbol":"AC017002.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111491943,"end":111494811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242951.1","gene_symbol":"AC007182.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75595805,"end":75596206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177640.15","gene_symbol":"CASC2","gene_name":"cancer susceptibility 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22933]","synonyms":"C10orf5","biotype":"antisense_RNA","ncbi_id":"255082","summary":null,"start":118046279,"end":118210153,"strand":1,"description":"cancer susceptibility 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22933]"}, {"versioned_ensembl_gene_id":"ENSG00000157349.16","gene_symbol":"DDX19B","gene_name":"DEAD-box helicase 19B [Source:HGNC Symbol;Acc:HGNC:2742]","synonyms":"DDX19,DBP5","biotype":"protein_coding","ncbi_id":"11269","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which exhibits RNA-dependent ATPase and ATP-dependent RNA-unwinding activities. This protein is recruited to the cytoplasmic fibrils of the nuclear pore complex, where it participates in the export of mRNA from the nucleus. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":70289663,"end":70335283,"strand":1,"description":"DEAD-box helicase 19B [Source:HGNC Symbol;Acc:HGNC:2742]"}, {"versioned_ensembl_gene_id":"ENSG00000239855.1","gene_symbol":"IGKV1-6","gene_name":"immunoglobulin kappa variable 1-6 [Source:HGNC Symbol;Acc:HGNC:5742]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28943","summary":null,"start":88966262,"end":88966767,"strand":-1,"description":"immunoglobulin kappa variable 1-6 [Source:HGNC Symbol;Acc:HGNC:5742]"}, {"versioned_ensembl_gene_id":"ENSG00000010318.20","gene_symbol":"PHF7","gene_name":"PHD finger protein 7 [Source:HGNC Symbol;Acc:HGNC:18458]","synonyms":"NYD-SP6,HSPC226","biotype":"protein_coding","ncbi_id":"51533","summary":"Spermatogenesis is a complex process regulated by extracellular and intracellular factors as well as cellular interactions among interstitial cells of the testis, Sertoli cells, and germ cells. This gene is expressed in the testis in Sertoli cells but not germ cells. The protein encoded by this gene contains plant homeodomain (PHD) finger domains, also known as leukemia associated protein (LAP) domains, believed to be involved in transcriptional regulation. The protein, which localizes to the nucleus of transfected cells, has been implicated in the transcriptional regulation of spermatogenesis. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":52410657,"end":52423641,"strand":1,"description":"PHD finger protein 7 [Source:HGNC Symbol;Acc:HGNC:18458]"}, {"versioned_ensembl_gene_id":"ENSG00000220157.4","gene_symbol":"HNRNPA1P12","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39130]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644037","summary":null,"start":80359080,"end":80360040,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39130]"}, {"versioned_ensembl_gene_id":"ENSG00000230545.6","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29724295,"end":29746743,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000211597.2","gene_symbol":"IGKJ1","gene_name":"immunoglobulin kappa joining 1 [Source:HGNC Symbol;Acc:HGNC:5719]","synonyms":"J1","biotype":"IG_J_gene","ncbi_id":"28950","summary":null,"start":88861886,"end":88861923,"strand":-1,"description":"immunoglobulin kappa joining 1 [Source:HGNC Symbol;Acc:HGNC:5719]"}, {"versioned_ensembl_gene_id":"ENSG00000173812.10","gene_symbol":"EIF1","gene_name":"eukaryotic translation initiation factor 1 [Source:HGNC Symbol;Acc:HGNC:3249]","synonyms":"SUI1,ISO1,EIF1A,EIF-1,A121","biotype":"protein_coding","ncbi_id":"10209","summary":null,"start":41688885,"end":41692668,"strand":1,"description":"eukaryotic translation initiation factor 1 [Source:HGNC Symbol;Acc:HGNC:3249]"}, {"versioned_ensembl_gene_id":"ENSG00000218896.1","gene_symbol":"TUBB8P2","gene_name":"tubulin beta 8 class VIII pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478982","summary":null,"start":143436216,"end":143436710,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42334]"}, {"versioned_ensembl_gene_id":"ENSG00000189007.15","gene_symbol":"ADAT2","gene_name":"adenosine deaminase, tRNA specific 2 [Source:HGNC Symbol;Acc:HGNC:21172]","synonyms":"TAD2,dJ20N2.1,DEADC1","biotype":"protein_coding","ncbi_id":"134637","summary":null,"start":143422832,"end":143450673,"strand":-1,"description":"adenosine deaminase, tRNA specific 2 [Source:HGNC Symbol;Acc:HGNC:21172]"}, {"versioned_ensembl_gene_id":"ENSG00000253633.1","gene_symbol":"AP002852.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102528740,"end":102538668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254568.1","gene_symbol":"AP003501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124883691,"end":124887789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173846.12","gene_symbol":"PLK3","gene_name":"polo like kinase 3 [Source:HGNC Symbol;Acc:HGNC:2154]","synonyms":"FNK,CNK,PRK","biotype":"protein_coding","ncbi_id":"1263","summary":"The protein encoded by this gene is a member of the highly conserved polo-like kinase family of serine/threonine kinases. Members of this family are characterized by an amino-terminal kinase domain and a carboxy-terminal bipartite polo box domain that functions as a substrate-binding motif and a cellular localization signal. Polo-like kinases are important regulators of cell cycle progression. This gene has also been implicated in stress responses and double-strand break repair. In human cell lines, this protein is reported to associate with centrosomes in a microtubule-dependent manner, and during mitosis, the protein becomes localized to the mitotic apparatus. Expression of a kinase-defective mutant results in abnormal cell morphology caused by changes in microtubule dynamics and mitotic arrest followed by apoptosis. [provided by RefSeq, Sep 2015]","start":44800225,"end":44805990,"strand":1,"description":"polo like kinase 3 [Source:HGNC Symbol;Acc:HGNC:2154]"}, {"versioned_ensembl_gene_id":"ENSG00000184986.10","gene_symbol":"TMEM121","gene_name":"transmembrane protein 121 [Source:HGNC Symbol;Acc:HGNC:20511]","synonyms":"TMEM121A,MGC4659,hole","biotype":"protein_coding","ncbi_id":"80757","summary":null,"start":105526603,"end":105530202,"strand":1,"description":"transmembrane protein 121 [Source:HGNC Symbol;Acc:HGNC:20511]"}, {"versioned_ensembl_gene_id":"ENSG00000160180.15","gene_symbol":"TFF3","gene_name":"trefoil factor 3 [Source:HGNC Symbol;Acc:HGNC:11757]","synonyms":"ITF,HITF","biotype":"protein_coding","ncbi_id":"7033","summary":"Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer and affect healing of the epithelium. This gene is expressed in goblet cells of the intestines and colon. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21. [provided by RefSeq, Jul 2008]","start":42311667,"end":42315651,"strand":-1,"description":"trefoil factor 3 [Source:HGNC Symbol;Acc:HGNC:11757]"}, {"versioned_ensembl_gene_id":"ENSG00000211595.2","gene_symbol":"IGKJ3","gene_name":"immunoglobulin kappa joining 3 [Source:HGNC Symbol;Acc:HGNC:5721]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28948","summary":null,"start":88861221,"end":88861258,"strand":-1,"description":"immunoglobulin kappa joining 3 [Source:HGNC Symbol;Acc:HGNC:5721]"}, {"versioned_ensembl_gene_id":"ENSG00000131094.3","gene_symbol":"C1QL1","gene_name":"complement C1q like 1 [Source:HGNC Symbol;Acc:HGNC:24182]","synonyms":"CRF,C1QTNF14,C1QRF","biotype":"protein_coding","ncbi_id":"10882","summary":null,"start":44959693,"end":44968071,"strand":-1,"description":"complement C1q like 1 [Source:HGNC Symbol;Acc:HGNC:24182]"}, {"versioned_ensembl_gene_id":"ENSG00000259082.1","gene_symbol":"LINC02314","gene_name":"long intergenic non-protein coding RNA 2314 [Source:HGNC Symbol;Acc:HGNC:53233]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507277","summary":null,"start":101442076,"end":101444315,"strand":1,"description":"long intergenic non-protein coding RNA 2314 [Source:HGNC Symbol;Acc:HGNC:53233]"}, {"versioned_ensembl_gene_id":"ENSG00000134569.9","gene_symbol":"LRP4","gene_name":"LDL receptor related protein 4 [Source:HGNC Symbol;Acc:HGNC:6696]","synonyms":"SOST2,MEGF7,LRP-4,CLSS","biotype":"protein_coding","ncbi_id":"4038","summary":"This gene encodes a member of the low-density lipoprotein receptor-related protein family. The encoded protein may be a regulator of Wnt signaling. Mutations in this gene are associated with Cenani-Lenz syndrome. [provided by RefSeq, May 2010]","start":46856868,"end":46918642,"strand":-1,"description":"LDL receptor related protein 4 [Source:HGNC Symbol;Acc:HGNC:6696]"}, {"versioned_ensembl_gene_id":"ENSG00000236248.1","gene_symbol":"AC104389.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5362615,"end":5362849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131771.13","gene_symbol":"PPP1R1B","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 1B [Source:HGNC Symbol;Acc:HGNC:9287]","synonyms":"FLJ20940,DARPP-32","biotype":"protein_coding","ncbi_id":"84152","summary":"This gene encodes a bifunctional signal transduction molecule. Dopaminergic and glutamatergic receptor stimulation regulates its phosphorylation and function as a kinase or phosphatase inhibitor. As a target for dopamine, this gene may serve as a therapeutic target for neurologic and psychiatric disorders. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":39626740,"end":39636626,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 1B [Source:HGNC Symbol;Acc:HGNC:9287]"}, {"versioned_ensembl_gene_id":"ENSG00000139675.11","gene_symbol":"HNRNPA1L2","gene_name":"heterogeneous nuclear ribonucleoprotein A1-like 2 [Source:HGNC Symbol;Acc:HGNC:27067]","synonyms":"LOC144983","biotype":"protein_coding","ncbi_id":"144983","summary":null,"start":52640786,"end":52643796,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1-like 2 [Source:HGNC Symbol;Acc:HGNC:27067]"}, {"versioned_ensembl_gene_id":"ENSG00000266921.1","gene_symbol":"AC006213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43996896,"end":44002836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163930.9","gene_symbol":"BAP1","gene_name":"BRCA1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:950]","synonyms":"UCHL2,KIAA0272,hucep-6","biotype":"protein_coding","ncbi_id":"8314","summary":"This gene belongs to the ubiquitin C-terminal hydrolase subfamily of deubiquitinating enzymes that are involved in the removal of ubiquitin from proteins. The encoded enzyme binds to the breast cancer type 1 susceptibility protein (BRCA1) via the RING finger domain of the latter and acts as a tumor suppressor. In addition, the enzyme may be involved in regulation of transcription, regulation of cell cycle and growth, response to DNA damage and chromatin dynamics. Germline mutations in this gene may be associated with tumor predisposition syndrome (TPDS), which involves increased risk of cancers including malignant mesothelioma, uveal melanoma and cutaneous melanoma. [provided by RefSeq, May 2013]","start":52401013,"end":52410350,"strand":-1,"description":"BRCA1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:950]"}, {"versioned_ensembl_gene_id":"ENSG00000111229.15","gene_symbol":"ARPC3","gene_name":"actin related protein 2/3 complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:706]","synonyms":"p21-Arc,ARC21","biotype":"protein_coding","ncbi_id":"10094","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been conserved through evolution and is implicated in the control of actin polymerization in cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":110434825,"end":110450422,"strand":-1,"description":"actin related protein 2/3 complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:706]"}, {"versioned_ensembl_gene_id":"ENSG00000235784.2","gene_symbol":"HNRNPA1P29","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39547]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421424","summary":null,"start":93394977,"end":93395855,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:39547]"}, {"versioned_ensembl_gene_id":"ENSG00000269745.1","gene_symbol":"AC006262.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46228964,"end":46230388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282864.1","gene_symbol":"AL356118.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91485793,"end":91486870,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179399.14","gene_symbol":"GPC5","gene_name":"glypican 5 [Source:HGNC Symbol;Acc:HGNC:4453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2262","summary":"Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. [provided by RefSeq, Jul 2008]","start":91398607,"end":92873682,"strand":1,"description":"glypican 5 [Source:HGNC Symbol;Acc:HGNC:4453]"}, {"versioned_ensembl_gene_id":"ENSG00000232885.1","gene_symbol":"GPC5-AS2","gene_name":"GPC5 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39887]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873970","summary":null,"start":92339794,"end":92340603,"strand":-1,"description":"GPC5 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39887]"}, {"versioned_ensembl_gene_id":"ENSG00000229557.1","gene_symbol":"LINC00379","gene_name":"long intergenic non-protein coding RNA 379 [Source:HGNC Symbol;Acc:HGNC:42705]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874150","summary":null,"start":91127613,"end":91131407,"strand":-1,"description":"long intergenic non-protein coding RNA 379 [Source:HGNC Symbol;Acc:HGNC:42705]"}, {"versioned_ensembl_gene_id":"ENSG00000235660.1","gene_symbol":"LINC00345","gene_name":"long intergenic non-protein coding RNA 345 [Source:HGNC Symbol;Acc:HGNC:42503]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370208","summary":null,"start":52484161,"end":52484680,"strand":-1,"description":"long intergenic non-protein coding RNA 345 [Source:HGNC Symbol;Acc:HGNC:42503]"}, {"versioned_ensembl_gene_id":"ENSG00000242317.1","gene_symbol":"AC121764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55493830,"end":55505261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129048.6","gene_symbol":"ACKR4","gene_name":"atypical chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:1611]","synonyms":"VSHK1,PPR1,CCX-CKR,CCRL1,CCR11,CCBP2","biotype":"protein_coding","ncbi_id":"51554","summary":"The protein encoded by this gene is a member of the G protein-coupled receptor family, and is a receptor for C-C type chemokines. This receptor has been shown to bind dendritic cell- and T cell-activated chemokines including CCL19/ELC, CCL21/SLC, and CCL25/TECK. A pseudogene of this gene is found on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2013]","start":132597237,"end":132618967,"strand":1,"description":"atypical chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:1611]"}, {"versioned_ensembl_gene_id":"ENSG00000236352.1","gene_symbol":"AC005220.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53940160,"end":53942508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197774.12","gene_symbol":"EME2","gene_name":"essential meiotic structure-specific endonuclease subunit 2 [Source:HGNC Symbol;Acc:HGNC:27289]","synonyms":"SLX2B,FLJ00151","biotype":"protein_coding","ncbi_id":"197342","summary":"EME2 forms a heterodimer with MUS81 (MIM 606591) that functions as an XPF (MIM 278760)-type flap/fork endonuclease in DNA repair (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008]","start":1773207,"end":1781708,"strand":1,"description":"essential meiotic structure-specific endonuclease subunit 2 [Source:HGNC Symbol;Acc:HGNC:27289]"}, {"versioned_ensembl_gene_id":"ENSG00000101974.14","gene_symbol":"ATP11C","gene_name":"ATPase phospholipid transporting 11C [Source:HGNC Symbol;Acc:HGNC:13554]","synonyms":"ATPIQ,ATPIG","biotype":"protein_coding","ncbi_id":"286410","summary":null,"start":139726346,"end":139945276,"strand":-1,"description":"ATPase phospholipid transporting 11C [Source:HGNC Symbol;Acc:HGNC:13554]"}, {"versioned_ensembl_gene_id":"ENSG00000170954.11","gene_symbol":"ZNF415","gene_name":"zinc finger protein 415 [Source:HGNC Symbol;Acc:HGNC:20636]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55786","summary":null,"start":53107879,"end":53133077,"strand":-1,"description":"zinc finger protein 415 [Source:HGNC Symbol;Acc:HGNC:20636]"}, {"versioned_ensembl_gene_id":"ENSG00000102805.14","gene_symbol":"CLN5","gene_name":"ceroid-lipofuscinosis, neuronal 5 [Source:HGNC Symbol;Acc:HGNC:2076]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1203","summary":"This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008]","start":76990660,"end":77019143,"strand":1,"description":"ceroid-lipofuscinosis, neuronal 5 [Source:HGNC Symbol;Acc:HGNC:2076]"}, {"versioned_ensembl_gene_id":"ENSG00000255311.5","gene_symbol":"AP002370.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83643602,"end":83725390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223956.2","gene_symbol":"LINC01767","gene_name":"long intergenic non-protein coding RNA 1767 [Source:HGNC Symbol;Acc:HGNC:52557]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378744","summary":null,"start":56414963,"end":56415966,"strand":1,"description":"long intergenic non-protein coding RNA 1767 [Source:HGNC Symbol;Acc:HGNC:52557]"}, {"versioned_ensembl_gene_id":"ENSG00000213489.3","gene_symbol":"AL627231.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125326897,"end":125328021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234229.8","gene_symbol":"LINC01505","gene_name":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]","synonyms":"RP11-308N19.1,RP11-308N19.1","biotype":"lincRNA","ncbi_id":"100996590","summary":null,"start":106664754,"end":106702662,"strand":1,"description":"long intergenic non-protein coding RNA 1505 [Source:HGNC Symbol;Acc:HGNC:51186]"}, {"versioned_ensembl_gene_id":"ENSG00000123243.14","gene_symbol":"ITIH5","gene_name":"inter-alpha-trypsin inhibitor heavy chain family member 5 [Source:HGNC Symbol;Acc:HGNC:21449]","synonyms":"MGC10848","biotype":"protein_coding","ncbi_id":"80760","summary":"This gene encodes a heavy chain component of one of the inter-alpha-trypsin inhibitor (ITI) family members. ITI proteins are involved in extracellular matrix stabilization and in the prevention of tumor metastasis. They are also structurally related plasma serine protease inhibitors and are composed of a light chain and varying numbers of heavy chains. This family member is thought to function as a tumor suppressor in breast and thyroid cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":7559270,"end":7666998,"strand":-1,"description":"inter-alpha-trypsin inhibitor heavy chain family member 5 [Source:HGNC Symbol;Acc:HGNC:21449]"}, {"versioned_ensembl_gene_id":"ENSG00000257851.2","gene_symbol":"HNRNPA3P10","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421413","summary":null,"start":51712469,"end":51713606,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48756]"}, {"versioned_ensembl_gene_id":"ENSG00000233079.1","gene_symbol":"LINC01755","gene_name":"long intergenic non-protein coding RNA 1755 [Source:HGNC Symbol;Acc:HGNC:52543]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378738","summary":null,"start":55945087,"end":55950119,"strand":1,"description":"long intergenic non-protein coding RNA 1755 [Source:HGNC Symbol;Acc:HGNC:52543]"}, {"versioned_ensembl_gene_id":"ENSG00000260122.1","gene_symbol":"AC068987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51809705,"end":51810600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283554.1","gene_symbol":"LINC02341","gene_name":"long intergenic non-protein coding RNA 2341 [Source:HGNC Symbol;Acc:HGNC:53261]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370177","summary":null,"start":42339188,"end":42485956,"strand":1,"description":"long intergenic non-protein coding RNA 2341 [Source:HGNC Symbol;Acc:HGNC:53261]"}, {"versioned_ensembl_gene_id":"ENSG00000230250.2","gene_symbol":"LINC01753","gene_name":"long intergenic non-protein coding RNA 1753 [Source:HGNC Symbol;Acc:HGNC:52541]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378739","summary":null,"start":55915607,"end":55944974,"strand":-1,"description":"long intergenic non-protein coding RNA 1753 [Source:HGNC Symbol;Acc:HGNC:52541]"}, {"versioned_ensembl_gene_id":"ENSG00000183207.13","gene_symbol":"RUVBL2","gene_name":"RuvB like AAA ATPase 2 [Source:HGNC Symbol;Acc:HGNC:10475]","synonyms":"TIP49b,TIP48,TIH2,RVB2,Reptin52,INO80J,ECP51","biotype":"protein_coding","ncbi_id":"10856","summary":"This gene encodes the second human homologue of the bacterial RuvB gene. Bacterial RuvB protein is a DNA helicase essential for homologous recombination and DNA double-strand break repair. Functional analysis showed that this gene product has both ATPase and DNA helicase activities. This gene is physically linked to the CGB/LHB gene cluster on chromosome 19q13.3, and is very close (55 nt) to the LHB gene, in the opposite orientation. [provided by RefSeq, Jul 2008]","start":48993448,"end":49015995,"strand":1,"description":"RuvB like AAA ATPase 2 [Source:HGNC Symbol;Acc:HGNC:10475]"}, {"versioned_ensembl_gene_id":"ENSG00000167637.16","gene_symbol":"ZNF283","gene_name":"zinc finger protein 283 [Source:HGNC Symbol;Acc:HGNC:13077]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284349","summary":null,"start":43827292,"end":43852017,"strand":1,"description":"zinc finger protein 283 [Source:HGNC Symbol;Acc:HGNC:13077]"}, {"versioned_ensembl_gene_id":"ENSG00000223493.9","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"SKIV2L1,HLP,SKIV2,DDX13,SKI2W,170A","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31941262,"end":31951933,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000271013.1","gene_symbol":"LRRC37A9P","gene_name":"leucine rich repeat containing 37 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:43813]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533790","summary":null,"start":35912635,"end":35918010,"strand":-1,"description":"leucine rich repeat containing 37 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:43813]"}, {"versioned_ensembl_gene_id":"ENSG00000215641.8","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RNF76,RFP","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28902991,"end":28923978,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000205302.6","gene_symbol":"SNX2","gene_name":"sorting nexin 2 [Source:HGNC Symbol;Acc:HGNC:11173]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6643","summary":"This gene belongs to the sorting nexin family whose members contain the phosphoinositide-binding phox (PX) domain. The encoded protein is a component of the retromer complex which plays a role in protein sorting in the endocytic pathway. This protein may form oligomeric complexes with other family members. Alternate splicing results in multiple transcript variants of this gene. Pseudogenes associated with this gene are located on chromosomes 1 and 7. [provided by RefSeq, May 2013]","start":122774996,"end":122830108,"strand":1,"description":"sorting nexin 2 [Source:HGNC Symbol;Acc:HGNC:11173]"}, {"versioned_ensembl_gene_id":"ENSG00000160838.13","gene_symbol":"LRRC71","gene_name":"leucine rich repeat containing 71 [Source:HGNC Symbol;Acc:HGNC:26556]","synonyms":"FLJ32884,C1orf92","biotype":"protein_coding","ncbi_id":"149499","summary":null,"start":156920650,"end":156933094,"strand":1,"description":"leucine rich repeat containing 71 [Source:HGNC Symbol;Acc:HGNC:26556]"}, {"versioned_ensembl_gene_id":"ENSG00000125944.19","gene_symbol":"HNRNPR","gene_name":"heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]","synonyms":"HNRPR,hnRNP-R","biotype":"protein_coding","ncbi_id":"10236","summary":"This gene encodes an RNA-binding protein that is a member of the spliceosome C complex, which functions in pre-mRNA processing and transport. The encoded protein also promotes transcription at the c-fos gene. Alternative splicing results in multiple transcript variants. There are pseudogenes for this gene on chromosomes 4, 11, and 10. [provided by RefSeq, Jul 2014]","start":23303771,"end":23344336,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]"}, {"versioned_ensembl_gene_id":"ENSG00000197275.13","gene_symbol":"RAD54B","gene_name":"RAD54 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:17228]","synonyms":"RDH54","biotype":"protein_coding","ncbi_id":"25788","summary":"The protein encoded by this gene belongs to the DEAD-like helicase superfamily. It shares similarity with Saccharomyces cerevisiae RAD54 and RDH54, both of which are involved in homologous recombination and repair of DNA. This protein binds to double-stranded DNA, and displays ATPase activity in the presence of DNA. This gene is highly expressed in testis and spleen, which suggests active roles in meiotic and mitotic recombination. Homozygous mutations of this gene were observed in primary lymphoma and colon cancer. [provided by RefSeq, Jul 2008]","start":94371960,"end":94475109,"strand":-1,"description":"RAD54 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:17228]"}, {"versioned_ensembl_gene_id":"ENSG00000091409.14","gene_symbol":"ITGA6","gene_name":"integrin subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:6142]","synonyms":"CD49f","biotype":"protein_coding","ncbi_id":"3655","summary":"The gene encodes a member of the integrin alpha chain family of proteins. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain that function in cell surface adhesion and signaling. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha 6 subunit. This subunit may associate with a beta 1 or beta 4 subunit to form an integrin that interacts with extracellular matrix proteins including members of the laminin family. The alpha 6 beta 4 integrin may promote tumorigenesis, while the alpha 6 beta 1 integrin may negatively regulate erbB2/HER2 signaling. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":172427354,"end":172506282,"strand":1,"description":"integrin subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:6142]"}, {"versioned_ensembl_gene_id":"ENSG00000149532.15","gene_symbol":"CPSF7","gene_name":"cleavage and polyadenylation specific factor 7 [Source:HGNC Symbol;Acc:HGNC:30098]","synonyms":"FLJ12529,CFIM59","biotype":"protein_coding","ncbi_id":"79869","summary":"Cleavage factor Im (CFIm) is one of six factors necessary for correct cleavage and polyadenylation of pre-mRNAs. CFIm is composed of three different subunits of 25, 59, and 68 kDa, and it functions as a heterotetramer, with a dimer of the 25 kDa subunit binding to two of the 59 or 68 kDa subunits. The protein encoded by this gene represents the 59 kDa subunit, which can interact with the splicing factor U2 snRNP Auxiliary Factor (U2AF) 65 to link the splicing and polyadenylation complexes. [provided by RefSeq, Oct 2016]","start":61402641,"end":61430031,"strand":-1,"description":"cleavage and polyadenylation specific factor 7 [Source:HGNC Symbol;Acc:HGNC:30098]"}, {"versioned_ensembl_gene_id":"ENSG00000232591.1","gene_symbol":"AL139125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7445558,"end":7471942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244217.1","gene_symbol":"RPS4XP10","gene_name":"ribosomal protein S4X pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35741]","synonyms":"RPS4P10","biotype":"processed_pseudogene","ncbi_id":"100271133","summary":null,"start":94352923,"end":94353653,"strand":1,"description":"ribosomal protein S4X pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35741]"}, {"versioned_ensembl_gene_id":"ENSG00000230636.1","gene_symbol":"RPL36P1","gene_name":"ribosomal protein L36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16338]","synonyms":"bA80K6.3","biotype":"processed_pseudogene","ncbi_id":"140697","summary":null,"start":52890162,"end":52890386,"strand":1,"description":"ribosomal protein L36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16338]"}, {"versioned_ensembl_gene_id":"ENSG00000131737.5","gene_symbol":"KRT34","gene_name":"keratin 34 [Source:HGNC Symbol;Acc:HGNC:6452]","synonyms":"Ha-4,KRTHA4","biotype":"protein_coding","ncbi_id":"3885","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41377650,"end":41382403,"strand":-1,"description":"keratin 34 [Source:HGNC Symbol;Acc:HGNC:6452]"}, {"versioned_ensembl_gene_id":"ENSG00000224091.1","gene_symbol":"AC104389.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5205041,"end":5207308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167861.15","gene_symbol":"HID1","gene_name":"HID1 domain containing [Source:HGNC Symbol;Acc:HGNC:15736]","synonyms":"HID-1,DMC1,C17orf28","biotype":"protein_coding","ncbi_id":"283987","summary":null,"start":74950743,"end":74973166,"strand":-1,"description":"HID1 domain containing [Source:HGNC Symbol;Acc:HGNC:15736]"}, {"versioned_ensembl_gene_id":"ENSG00000225211.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31665195,"end":31669285,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000214428.3","gene_symbol":"NPM1P10","gene_name":"nucleophosmin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:7912]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10837","summary":null,"start":104025540,"end":104026763,"strand":-1,"description":"nucleophosmin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:7912]"}, {"versioned_ensembl_gene_id":"ENSG00000161048.11","gene_symbol":"NAPEPLD","gene_name":"N-acyl phosphatidylethanolamine phospholipase D [Source:HGNC Symbol;Acc:HGNC:21683]","synonyms":"NAPE-PLD,FMP30,C7orf18","biotype":"protein_coding","ncbi_id":"222236","summary":"NAPEPLD is a phospholipase D type enzyme that catalyzes the release of N-acylethanolamine (NAE) from N-acyl-phosphatidylethanolamine (NAPE) in the second step of the biosynthesis of N-acylethanolamine (Okamoto et al., 2004 [PubMed 14634025]).[supplied by OMIM, Oct 2008]","start":103099776,"end":103149560,"strand":-1,"description":"N-acyl phosphatidylethanolamine phospholipase D [Source:HGNC Symbol;Acc:HGNC:21683]"}, {"versioned_ensembl_gene_id":"ENSG00000217120.1","gene_symbol":"Z98755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103002514,"end":103003897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259318.1","gene_symbol":"AL356801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55394940,"end":55395233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148219.16","gene_symbol":"ASTN2","gene_name":"astrotactin 2 [Source:HGNC Symbol;Acc:HGNC:17021]","synonyms":"KIAA0634","biotype":"protein_coding","ncbi_id":"23245","summary":"This gene encodes a protein that is expressed in the brain and may function in neuronal migration, based on functional studies of the related astrotactin 1 gene in human and mouse. A deletion at this locus has been associated with schizophrenia. Multiple transcript variants encoding different proteins have been found for this locus. [provided by RefSeq, May 2010]","start":116425225,"end":117415070,"strand":-1,"description":"astrotactin 2 [Source:HGNC Symbol;Acc:HGNC:17021]"}, {"versioned_ensembl_gene_id":"ENSG00000250258.1","gene_symbol":"AC008496.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79774348,"end":79816190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165917.9","gene_symbol":"RAPSN","gene_name":"receptor associated protein of the synapse [Source:HGNC Symbol;Acc:HGNC:9863]","synonyms":"RNF205,CMS1E,CMS1D","biotype":"protein_coding","ncbi_id":"5913","summary":"This gene encodes a member of a family of proteins that are receptor associated proteins of the synapse. The encoded protein contains a conserved cAMP-dependent protein kinase phosphorylation site, and plays a critical role in clustering and anchoring nicotinic acetylcholine receptors at synaptic sites by linking the receptors to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin. Mutations in this gene may play a role in postsynaptic congenital myasthenic syndromes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2011]","start":47437757,"end":47449178,"strand":-1,"description":"receptor associated protein of the synapse [Source:HGNC Symbol;Acc:HGNC:9863]"}, {"versioned_ensembl_gene_id":"ENSG00000172757.12","gene_symbol":"CFL1","gene_name":"cofilin 1 [Source:HGNC Symbol;Acc:HGNC:1874]","synonyms":"CFL","biotype":"protein_coding","ncbi_id":"1072","summary":"The protein encoded by this gene can polymerize and depolymerize F-actin and G-actin in a pH-dependent manner. Increased phosphorylation of this protein by LIM kinase aids in Rho-induced reorganization of the actin cytoskeleton. Cofilin is a widely distributed intracellular actin-modulating protein that binds and depolymerizes filamentous F-actin and inhibits the polymerization of monomeric G-actin in a pH-dependent manner. It is involved in the translocation of actin-cofilin complex from cytoplasm to nucleus.[supplied by OMIM, Apr 2004]","start":65823022,"end":65862026,"strand":-1,"description":"cofilin 1 [Source:HGNC Symbol;Acc:HGNC:1874]"}, {"versioned_ensembl_gene_id":"ENSG00000187123.14","gene_symbol":"LYPD6","gene_name":"LY6/PLAUR domain containing 6 [Source:HGNC Symbol;Acc:HGNC:28751]","synonyms":"MGC52057","biotype":"protein_coding","ncbi_id":"130574","summary":"Members of the LY6 protein family (see SLURP1; MIM 606119), such as LYPD6, have at least one 80-amino acid LU domain that contains 10 conserved cysteines with a defined disulfide-bonding pattern (Zhang et al., 2010 [PubMed 19653121]).[supplied by OMIM, Apr 2010]","start":149329985,"end":149474148,"strand":1,"description":"LY6/PLAUR domain containing 6 [Source:HGNC Symbol;Acc:HGNC:28751]"}, {"versioned_ensembl_gene_id":"ENSG00000116396.14","gene_symbol":"KCNC4","gene_name":"potassium voltage-gated channel subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:6236]","synonyms":"Kv3.4,HKSHIIIC,C1orf30","biotype":"protein_coding","ncbi_id":"3749","summary":"The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies. Based on sequence similarity, this gene is similar to the Shaw subfamily. The protein encoded by this gene belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes. It generates atypical voltage-dependent transient current that may be important for neuronal excitability. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jul 2010]","start":110211343,"end":110283100,"strand":1,"description":"potassium voltage-gated channel subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:6236]"}, {"versioned_ensembl_gene_id":"ENSG00000282852.1","gene_symbol":"AL137790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110256754,"end":110256930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236343.1","gene_symbol":"EI24P4","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44589]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420072","summary":null,"start":145005058,"end":145006135,"strand":1,"description":"EI24, autophagy associated transmembrane protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44589]"}, {"versioned_ensembl_gene_id":"ENSG00000198242.13","gene_symbol":"RPL23A","gene_name":"ribosomal protein L23a [Source:HGNC Symbol;Acc:HGNC:10317]","synonyms":"L23A","biotype":"protein_coding","ncbi_id":"6147","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L23P family of ribosomal proteins. It is located in the cytoplasm. The protein may be one of the target molecules involved in mediating growth inhibition by interferon. In yeast, the corresponding protein binds to a specific site on the 26S rRNA. This gene is co-transcribed with the U42A, U42B, U101A, and U101B small nucleolar RNA genes, which are located in its third, first, second, and fourth introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":28719393,"end":28724359,"strand":1,"description":"ribosomal protein L23a [Source:HGNC Symbol;Acc:HGNC:10317]"}, {"versioned_ensembl_gene_id":"ENSG00000235881.2","gene_symbol":"AC114776.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110709575,"end":110716595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275237.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789912,"end":54800893,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000197428.3","gene_symbol":"OR51D1","gene_name":"olfactory receptor family 51 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15193]","synonyms":"OR51D1Q","biotype":"protein_coding","ncbi_id":"390038","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4637477,"end":4643060,"strand":1,"description":"olfactory receptor family 51 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:15193]"}, {"versioned_ensembl_gene_id":"ENSG00000166035.10","gene_symbol":"LIPC","gene_name":"lipase C, hepatic type [Source:HGNC Symbol;Acc:HGNC:6619]","synonyms":"HTGL,HL","biotype":"protein_coding","ncbi_id":"3990","summary":"LIPC encodes hepatic triglyceride lipase, which is expressed in liver. LIPC has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. [provided by RefSeq, Jul 2008]","start":58410569,"end":58569843,"strand":1,"description":"lipase C, hepatic type [Source:HGNC Symbol;Acc:HGNC:6619]"}, {"versioned_ensembl_gene_id":"ENSG00000275012.1","gene_symbol":"AC011476.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54948864,"end":54948993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196859.7","gene_symbol":"KRT39","gene_name":"keratin 39 [Source:HGNC Symbol;Acc:HGNC:32971]","synonyms":"KA35","biotype":"protein_coding","ncbi_id":"390792","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40958417,"end":40966892,"strand":-1,"description":"keratin 39 [Source:HGNC Symbol;Acc:HGNC:32971]"}, {"versioned_ensembl_gene_id":"ENSG00000278892.1","gene_symbol":"AP002371.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93071529,"end":93072031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177736.4","gene_symbol":"FXNP2","gene_name":"frataxin pseuodgene 2 [Source:HGNC Symbol;Acc:HGNC:51607]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418706","summary":null,"start":124968294,"end":124968840,"strand":-1,"description":"frataxin pseuodgene 2 [Source:HGNC Symbol;Acc:HGNC:51607]"}, {"versioned_ensembl_gene_id":"ENSG00000251293.1","gene_symbol":"AC008574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120245448,"end":120333502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258407.1","gene_symbol":"AL157955.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88010787,"end":88015611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157693.14","gene_symbol":"TMEM268","gene_name":"transmembrane protein 268 [Source:HGNC Symbol;Acc:HGNC:24513]","synonyms":"FLJ38045,DKFZp547P234,C9orf91","biotype":"protein_coding","ncbi_id":"203197","summary":null,"start":114611206,"end":114646422,"strand":1,"description":"transmembrane protein 268 [Source:HGNC Symbol;Acc:HGNC:24513]"}, {"versioned_ensembl_gene_id":"ENSG00000250573.1","gene_symbol":"AC006499.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10259445,"end":10260138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236101.1","gene_symbol":"RAC1P7","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874390","summary":null,"start":234026851,"end":234027227,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42007]"}, {"versioned_ensembl_gene_id":"ENSG00000225045.1","gene_symbol":"MTND5P27","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42289]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873264","summary":null,"start":82815809,"end":82817528,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42289]"}, {"versioned_ensembl_gene_id":"ENSG00000152348.15","gene_symbol":"ATG10","gene_name":"autophagy related 10 [Source:HGNC Symbol;Acc:HGNC:20315]","synonyms":"FLJ13954,DKFZP586I0418,APG10L","biotype":"protein_coding","ncbi_id":"83734","summary":"Autophagy is a process for the bulk degradation of cytosolic compartments by lysosomes. ATG10 is an E2-like enzyme involved in 2 ubiquitin-like modifications essential for autophagosome formation: ATG12 (MIM 609608)-ATG5 (MIM 604261) conjugation and modification of a soluble form of MAP-LC3 (MAP1LC3A; MIM 601242), a homolog of yeast Apg8, to a membrane-bound form (Nemoto et al., 2003 [PubMed 12890687]).[supplied by OMIM, Mar 2008]","start":81972025,"end":82276857,"strand":1,"description":"autophagy related 10 [Source:HGNC Symbol;Acc:HGNC:20315]"}, {"versioned_ensembl_gene_id":"ENSG00000034677.12","gene_symbol":"RNF19A","gene_name":"ring finger protein 19A, RBR E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:13432]","synonyms":"RNF19,dorfin,DKFZp566B1346","biotype":"protein_coding","ncbi_id":"25897","summary":"This gene encodes a member of the ring between ring fingers (RBR) protein family, and the encoded protein contains two RING-finger motifs and an in between RING fingers motif. This protein is an E3 ubiquitin ligase that is localized to Lewy bodies, and ubiquitylates synphilin-1, which is an interacting protein of alpha synuclein in neurons. The encoded protein may be involved in amyotrophic lateral sclerosis and Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":100257060,"end":100336218,"strand":-1,"description":"ring finger protein 19A, RBR E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:13432]"}, {"versioned_ensembl_gene_id":"ENSG00000256594.8","gene_symbol":"AC010186.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9648047,"end":9658412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232798.1","gene_symbol":"CR769767.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39892550,"end":39892895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266850.1","gene_symbol":"AC090912.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22723491,"end":22907721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284116.1","gene_symbol":"AL772307.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":39983793,"end":40106611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256442.1","gene_symbol":"AC010186.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9647014,"end":9648009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204463.12","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31639028,"end":31652705,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000143153.12","gene_symbol":"ATP1B1","gene_name":"ATPase Na+/K+ transporting subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:804]","synonyms":"ATP1B","biotype":"protein_coding","ncbi_id":"481","summary":"The protein encoded by this gene belongs to the family of Na+/K+ and H+/K+ ATPases beta chain proteins, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The beta subunit regulates, through assembly of alpha/beta heterodimers, the number of sodium pumps transported to the plasma membrane. The glycoprotein subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes a beta 1 subunit. Alternatively spliced transcript variants encoding different isoforms have been described, but their biological validity is not known. [provided by RefSeq, Mar 2010]","start":169105697,"end":169132722,"strand":1,"description":"ATPase Na+/K+ transporting subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:804]"}, {"versioned_ensembl_gene_id":"ENSG00000273890.1","gene_symbol":"AC034102.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56010091,"end":56010574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231253.1","gene_symbol":"LINC01640","gene_name":"long intergenic non-protein coding RNA 1640 [Source:HGNC Symbol;Acc:HGNC:52427]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373006","summary":null,"start":33108529,"end":33116294,"strand":1,"description":"long intergenic non-protein coding RNA 1640 [Source:HGNC Symbol;Acc:HGNC:52427]"}, {"versioned_ensembl_gene_id":"ENSG00000167977.8","gene_symbol":"KCTD5","gene_name":"potassium channel tetramerization domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21423]","synonyms":"FLJ20040","biotype":"protein_coding","ncbi_id":"54442","summary":null,"start":2682475,"end":2709030,"strand":1,"description":"potassium channel tetramerization domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21423]"}, {"versioned_ensembl_gene_id":"ENSG00000279901.1","gene_symbol":"AC092117.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2683106,"end":2684764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249483.1","gene_symbol":"AC026726.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81851601,"end":81852201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278070.2","gene_symbol":"GOLGA8EP","gene_name":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]","synonyms":"GOLGA8E","biotype":"unprocessed_pseudogene","ncbi_id":"390535","summary":null,"start":23160896,"end":23171217,"strand":1,"description":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]"}, {"versioned_ensembl_gene_id":"ENSG00000273179.1","gene_symbol":"AC092535.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1167778,"end":1168174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229967.1","gene_symbol":"AF274855.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151904431,"end":151913968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284018.1","gene_symbol":"AC018793.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4233288,"end":4233872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250788.1","gene_symbol":"TUBB8P4","gene_name":"tubulin beta 8 class VIII pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42185]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"260338","summary":null,"start":34164773,"end":34166954,"strand":-1,"description":"tubulin beta 8 class VIII pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42185]"}, {"versioned_ensembl_gene_id":"ENSG00000260838.3","gene_symbol":"AC022893.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72947150,"end":72950445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178662.15","gene_symbol":"CSRNP3","gene_name":"cysteine and serine rich nuclear protein 3 [Source:HGNC Symbol;Acc:HGNC:30729]","synonyms":"TAIP-2,PPP1R73,FLJ32093,FAM130A2","biotype":"protein_coding","ncbi_id":"80034","summary":null,"start":165469647,"end":165689407,"strand":1,"description":"cysteine and serine rich nuclear protein 3 [Source:HGNC Symbol;Acc:HGNC:30729]"}, {"versioned_ensembl_gene_id":"ENSG00000203601.3","gene_symbol":"LINC00970","gene_name":"long intergenic non-protein coding RNA 970 [Source:HGNC Symbol;Acc:HGNC:48730]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101978719","summary":null,"start":168903905,"end":169087005,"strand":-1,"description":"long intergenic non-protein coding RNA 970 [Source:HGNC Symbol;Acc:HGNC:48730]"}, {"versioned_ensembl_gene_id":"ENSG00000213063.3","gene_symbol":"RPL29P7","gene_name":"ribosomal protein L29 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36859]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270972","summary":null,"start":168938467,"end":168938923,"strand":1,"description":"ribosomal protein L29 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36859]"}, {"versioned_ensembl_gene_id":"ENSG00000174715.7","gene_symbol":"AC020890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138643874,"end":138644694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277498.1","gene_symbol":"AC107081.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61858137,"end":61860298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230621.1","gene_symbol":"AC068138.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":225992981,"end":225993197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148290.9","gene_symbol":"SURF1","gene_name":"SURF1, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:11474]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6834","summary":"This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. [provided by RefSeq, Jul 2008]","start":133351755,"end":133356676,"strand":-1,"description":"SURF1, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:11474]"}, {"versioned_ensembl_gene_id":"ENSG00000132837.14","gene_symbol":"DMGDH","gene_name":"dimethylglycine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29958","summary":"This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":78997606,"end":79236038,"strand":-1,"description":"dimethylglycine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:24475]"}, {"versioned_ensembl_gene_id":"ENSG00000254139.1","gene_symbol":"AC104051.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57746149,"end":57750199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270859.1","gene_symbol":"AC099785.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242671140,"end":242671576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253871.1","gene_symbol":"AC068075.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57343787,"end":57364857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224431.1","gene_symbol":"AC063976.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132199456,"end":132203487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238228.1","gene_symbol":"OR7E7P","gene_name":"olfactory receptor family 7 subfamily E member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:8457]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392752","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":97946987,"end":97947998,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:8457]"}, {"versioned_ensembl_gene_id":"ENSG00000135372.8","gene_symbol":"NAT10","gene_name":"N-acetyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:29830]","synonyms":"NET43,Kre33,KIAA1709,hALP,FLJ12179,FLJ10774","biotype":"protein_coding","ncbi_id":"55226","summary":"The protein encoded by this gene is an RNA cytidine acetyltransferase involved in histone acetylation, tRNA acetylation, the biosynthesis of 18S rRNA, and the enhancement of nuclear architecture and chromatin organization. [provided by RefSeq, Oct 2016]","start":34105602,"end":34147670,"strand":1,"description":"N-acetyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:29830]"}, {"versioned_ensembl_gene_id":"ENSG00000197208.5","gene_symbol":"SLC22A4","gene_name":"solute carrier family 22 member 4 [Source:HGNC Symbol;Acc:HGNC:10968]","synonyms":"OCTN1,MGC34546,DFNB60","biotype":"protein_coding","ncbi_id":"6583","summary":"Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is an organic cation transporter and plasma integral membrane protein containing eleven putative transmembrane domains as well as a nucleotide-binding site motif. Transport by this protein is at least partially ATP-dependent. [provided by RefSeq, Jul 2008]","start":132294443,"end":132344206,"strand":1,"description":"solute carrier family 22 member 4 [Source:HGNC Symbol;Acc:HGNC:10968]"}, {"versioned_ensembl_gene_id":"ENSG00000168216.10","gene_symbol":"LMBRD1","gene_name":"LMBR1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23038]","synonyms":"FLJ11240,cblF,C6orf209,bA810I22.1","biotype":"protein_coding","ncbi_id":"55788","summary":"This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.[provided by RefSeq, Oct 2009]","start":69675802,"end":69797111,"strand":-1,"description":"LMBR1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23038]"}, {"versioned_ensembl_gene_id":"ENSG00000172922.8","gene_symbol":"RNASEH2C","gene_name":"ribonuclease H2 subunit C [Source:HGNC Symbol;Acc:HGNC:24116]","synonyms":"AYP1,AGS3","biotype":"protein_coding","ncbi_id":"84153","summary":"This gene encodes a ribonuclease H subunit that can cleave ribonucleotides from RNA:DNA duplexes. Mutations in this gene cause Aicardi-Goutieres syndrome-3, a disease that causes severe neurologic dysfunction. A pseudogene for this gene has been identified on chromosome Y, near the sex determining region Y (SRY) gene. [provided by RefSeq, Jul 2008]","start":65714896,"end":65720947,"strand":-1,"description":"ribonuclease H2 subunit C [Source:HGNC Symbol;Acc:HGNC:24116]"}, {"versioned_ensembl_gene_id":"ENSG00000273403.1","gene_symbol":"AC107294.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184741937,"end":184742462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272922.1","gene_symbol":"AC107294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184742818,"end":184743284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050327.14","gene_symbol":"ARHGEF5","gene_name":"Rho guanine nucleotide exchange factor 5 [Source:HGNC Symbol;Acc:HGNC:13209]","synonyms":"TIM1,TIM,P60,GEF5","biotype":"protein_coding","ncbi_id":"7984","summary":"Rho GTPases play a fundamental role in numerous cellular processes initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form a complex with G proteins and stimulate Rho-dependent signals. This protein may be involved in the control of cytoskeletal organization. [provided by RefSeq, Jul 2008]","start":144355288,"end":144380632,"strand":1,"description":"Rho guanine nucleotide exchange factor 5 [Source:HGNC Symbol;Acc:HGNC:13209]"}, {"versioned_ensembl_gene_id":"ENSG00000264040.1","gene_symbol":"AC022662.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67602692,"end":67603022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263424.1","gene_symbol":"AC110597.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67506589,"end":67514030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129009.12","gene_symbol":"ISLR","gene_name":"immunoglobulin superfamily containing leucine rich repeat [Source:HGNC Symbol;Acc:HGNC:6133]","synonyms":"HsT17563","biotype":"protein_coding","ncbi_id":"3671","summary":null,"start":74173671,"end":74176872,"strand":1,"description":"immunoglobulin superfamily containing leucine rich repeat [Source:HGNC Symbol;Acc:HGNC:6133]"}, {"versioned_ensembl_gene_id":"ENSG00000283285.1","gene_symbol":"AC011460.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51914675,"end":51917703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205307.11","gene_symbol":"SAP25","gene_name":"Sin3A associated protein 25 [Source:HGNC Symbol;Acc:HGNC:41908]","synonyms":"FLJ00248","biotype":"protein_coding","ncbi_id":"100316904","summary":null,"start":100572228,"end":100573820,"strand":-1,"description":"Sin3A associated protein 25 [Source:HGNC Symbol;Acc:HGNC:41908]"}, {"versioned_ensembl_gene_id":"ENSG00000255010.1","gene_symbol":"AP001767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83106580,"end":83106961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167525.13","gene_symbol":"PROCA1","gene_name":"protein interacting with cyclin A1 [Source:HGNC Symbol;Acc:HGNC:28600]","synonyms":"MGC39650","biotype":"protein_coding","ncbi_id":"147011","summary":null,"start":28703197,"end":28711854,"strand":-1,"description":"protein interacting with cyclin A1 [Source:HGNC Symbol;Acc:HGNC:28600]"}, {"versioned_ensembl_gene_id":"ENSG00000132554.19","gene_symbol":"RGS22","gene_name":"regulator of G protein signaling 22 [Source:HGNC Symbol;Acc:HGNC:24499]","synonyms":"PRTD-NY2,DKFZP434I092,CT145","biotype":"protein_coding","ncbi_id":"26166","summary":null,"start":99960936,"end":100131268,"strand":-1,"description":"regulator of G protein signaling 22 [Source:HGNC Symbol;Acc:HGNC:24499]"}, {"versioned_ensembl_gene_id":"ENSG00000145685.13","gene_symbol":"LHFPL2","gene_name":"LHFPL tetraspan subfamily member 2 [Source:HGNC Symbol;Acc:HGNC:6588]","synonyms":"KIAA0206","biotype":"protein_coding","ncbi_id":"10184","summary":"This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":78485215,"end":78770021,"strand":-1,"description":"LHFPL tetraspan subfamily member 2 [Source:HGNC Symbol;Acc:HGNC:6588]"}, {"versioned_ensembl_gene_id":"ENSG00000231404.2","gene_symbol":"RAC1P3","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31833]","synonyms":"Psi3Rac1","biotype":"processed_pseudogene","ncbi_id":"492295","summary":null,"start":41287741,"end":41288320,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31833]"}, {"versioned_ensembl_gene_id":"ENSG00000253134.1","gene_symbol":"AC025437.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158275711,"end":158278813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248838.2","gene_symbol":"PGAM1P13","gene_name":"phosphoglycerate mutase 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42461]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129815","summary":null,"start":107647279,"end":107648032,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42461]"}, {"versioned_ensembl_gene_id":"ENSG00000261594.3","gene_symbol":"TPBGL","gene_name":"trophoblast glycoprotein like [Source:HGNC Symbol;Acc:HGNC:44159]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507050","summary":null,"start":75240905,"end":75243697,"strand":1,"description":"trophoblast glycoprotein like [Source:HGNC Symbol;Acc:HGNC:44159]"}, {"versioned_ensembl_gene_id":"ENSG00000279372.1","gene_symbol":"AC137723.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82035403,"end":82035800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105880.4","gene_symbol":"DLX5","gene_name":"distal-less homeobox 5 [Source:HGNC Symbol;Acc:HGNC:2918]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1749","summary":"This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. [provided by RefSeq, Jul 2008]","start":97020392,"end":97025097,"strand":-1,"description":"distal-less homeobox 5 [Source:HGNC Symbol;Acc:HGNC:2918]"}, {"versioned_ensembl_gene_id":"ENSG00000263874.2","gene_symbol":"LINC00672","gene_name":"long intergenic non-protein coding RNA 672 [Source:HGNC Symbol;Acc:HGNC:44353]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505576","summary":null,"start":38925168,"end":38929384,"strand":1,"description":"long intergenic non-protein coding RNA 672 [Source:HGNC Symbol;Acc:HGNC:44353]"}, {"versioned_ensembl_gene_id":"ENSG00000237131.1","gene_symbol":"AL021397.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168215405,"end":168215652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234076.1","gene_symbol":"TPRG1-AS1","gene_name":"TPRG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42391]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874043","summary":null,"start":188941715,"end":188947639,"strand":-1,"description":"TPRG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42391]"}, {"versioned_ensembl_gene_id":"ENSG00000258439.1","gene_symbol":"AC007956.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74658049,"end":74658590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250815.1","gene_symbol":"AC105384.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53927499,"end":53928138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248343.1","gene_symbol":"AC096576.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21697450,"end":21719026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167562.12","gene_symbol":"ZNF701","gene_name":"zinc finger protein 701 [Source:HGNC Symbol;Acc:HGNC:25597]","synonyms":"FLJ10891","biotype":"protein_coding","ncbi_id":"55762","summary":null,"start":52555457,"end":52587174,"strand":1,"description":"zinc finger protein 701 [Source:HGNC Symbol;Acc:HGNC:25597]"}, {"versioned_ensembl_gene_id":"ENSG00000242697.2","gene_symbol":"RPL5P12","gene_name":"ribosomal protein L5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36221]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270833","summary":null,"start":98025390,"end":98026240,"strand":1,"description":"ribosomal protein L5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36221]"}, {"versioned_ensembl_gene_id":"ENSG00000066032.18","gene_symbol":"CTNNA2","gene_name":"catenin alpha 2 [Source:HGNC Symbol;Acc:HGNC:2510]","synonyms":"CT114,CAP-R","biotype":"protein_coding","ncbi_id":"1496","summary":null,"start":79185231,"end":80648861,"strand":1,"description":"catenin alpha 2 [Source:HGNC Symbol;Acc:HGNC:2510]"}, {"versioned_ensembl_gene_id":"ENSG00000231468.2","gene_symbol":"PRDX3P2","gene_name":"peroxiredoxin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39265]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128092","summary":null,"start":28526318,"end":28527227,"strand":-1,"description":"peroxiredoxin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39265]"}, {"versioned_ensembl_gene_id":"ENSG00000211854.1","gene_symbol":"TRAJ35","gene_name":"T-cell receptor alpha joining 35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12065]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28720","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22506644,"end":22506702,"strand":1,"description":"T-cell receptor alpha joining 35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12065]"}, {"versioned_ensembl_gene_id":"ENSG00000276131.1","gene_symbol":"AC009118.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58392153,"end":58392807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231332.2","gene_symbol":"OOEP-AS1","gene_name":"OOEP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39192]","synonyms":"OOEP-AS","biotype":"antisense_RNA","ncbi_id":"106478938","summary":null,"start":73369704,"end":73387717,"strand":1,"description":"OOEP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39192]"}, {"versioned_ensembl_gene_id":"ENSG00000236740.6","gene_symbol":"AL033384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53930022,"end":53997667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176302.12","gene_symbol":"FOXR1","gene_name":"forkhead box R1 [Source:HGNC Symbol;Acc:HGNC:29980]","synonyms":"FOXN5,DLNB13","biotype":"protein_coding","ncbi_id":"283150","summary":"This gene encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix-turn-helix proteins with a core DNA-binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. This forkhead box protein lacks the C-terminal basic region found in many other FOX family members. It is located within the 11q23.3 region which is commonly deleted in neuroblastomas. [provided by RefSeq, Jul 2008]","start":118971707,"end":118981291,"strand":1,"description":"forkhead box R1 [Source:HGNC Symbol;Acc:HGNC:29980]"}, {"versioned_ensembl_gene_id":"ENSG00000206977.1","gene_symbol":"SNORA8","gene_name":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]","synonyms":"ACA8","biotype":"snoRNA","ncbi_id":"654320","summary":null,"start":41832854,"end":41832993,"strand":1,"description":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]"}, {"versioned_ensembl_gene_id":"ENSG00000275744.4","gene_symbol":"SLC2A11","gene_name":"solute carrier family 2 member 11 [Source:HGNC Symbol;Acc:HGNC:14239]","synonyms":"GLUT11,GLUT10","biotype":"protein_coding","ncbi_id":"66035","summary":"This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":23856703,"end":23886309,"strand":1,"description":"solute carrier family 2 member 11 [Source:HGNC Symbol;Acc:HGNC:14239]"}, {"versioned_ensembl_gene_id":"ENSG00000228551.1","gene_symbol":"SNRPGP9","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39328]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506574","summary":null,"start":109251422,"end":109251646,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39328]"}, {"versioned_ensembl_gene_id":"ENSG00000276882.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54921821,"end":54938615,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000132464.11","gene_symbol":"ENAM","gene_name":"enamelin [Source:HGNC Symbol;Acc:HGNC:3344]","synonyms":"AIH2","biotype":"protein_coding","ncbi_id":"10117","summary":"Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene encodes the largest protein in the enamel matrix of developing teeth. The protein is involved in the mineralization and structural organization of enamel. Defects in this gene result in amelogenesis imperfect type 1C.[provided by RefSeq, Oct 2009]","start":70628744,"end":70686816,"strand":1,"description":"enamelin [Source:HGNC Symbol;Acc:HGNC:3344]"}, {"versioned_ensembl_gene_id":"ENSG00000258594.1","gene_symbol":"AC021979.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27621534,"end":27629289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275905.1","gene_symbol":"AP003789.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106980967,"end":106981571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232512.6","gene_symbol":"AP000233.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25095022,"end":25103670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274600.1","gene_symbol":"RIMBP3B","gene_name":"RIMS binding protein 3B [Source:HGNC Symbol;Acc:HGNC:33891]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440804","summary":null,"start":21383374,"end":21389478,"strand":1,"description":"RIMS binding protein 3B [Source:HGNC Symbol;Acc:HGNC:33891]"}, {"versioned_ensembl_gene_id":"ENSG00000117153.15","gene_symbol":"KLHL12","gene_name":"kelch like family member 12 [Source:HGNC Symbol;Acc:HGNC:19360]","synonyms":"C3IP1","biotype":"protein_coding","ncbi_id":"59349","summary":"This gene encodes a member of the KLHL (Kelch-like) family of proteins. This protein has been identified as an autoantigen in the autoimmune disease Sjogren's syndrome and as a potential biomarker in primary biliary cirrhosis. This protein may act as a substrate adaptor of the Cullin-3 ubiquitin ligase complex to promote substrate-specific ubiquitylation. Ubiquitylation by this complex has been shown to regulate the Wnt signaling pathway as well as COPII vesicle coat size. A pseudogene has been identified on chromosome 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":202891100,"end":202928636,"strand":-1,"description":"kelch like family member 12 [Source:HGNC Symbol;Acc:HGNC:19360]"}, {"versioned_ensembl_gene_id":"ENSG00000211843.1","gene_symbol":"TRAJ46","gene_name":"T-cell receptor alpha joining 46 [Source:HGNC Symbol;Acc:HGNC:12077]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28709","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22493403,"end":22493465,"strand":1,"description":"T-cell receptor alpha joining 46 [Source:HGNC Symbol;Acc:HGNC:12077]"}, {"versioned_ensembl_gene_id":"ENSG00000196535.15","gene_symbol":"MYO18A","gene_name":"myosin XVIIIA [Source:HGNC Symbol;Acc:HGNC:31104]","synonyms":"MysPDZ,KIAA0216","biotype":"protein_coding","ncbi_id":"399687","summary":"The protein encoded by this gene can bind GOLPH3, linking the Golgi to the cytoskeleton and influencing Golgi membrane trafficking. The encoded protein is also part of a complex that assembles lamellar actomyosin bundles and may be required for cell migration. [provided by RefSeq, Oct 2016]","start":29071124,"end":29180412,"strand":-1,"description":"myosin XVIIIA [Source:HGNC Symbol;Acc:HGNC:31104]"}, {"versioned_ensembl_gene_id":"ENSG00000251356.1","gene_symbol":"RAB5CP2","gene_name":"RAB5C, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45106]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"133789","summary":null,"start":91476382,"end":91477018,"strand":1,"description":"RAB5C, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45106]"}, {"versioned_ensembl_gene_id":"ENSG00000258406.1","gene_symbol":"AL445383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43274824,"end":43275697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260726.2","gene_symbol":"AC023827.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48718083,"end":48719143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187516.6","gene_symbol":"HYPM","gene_name":"huntingtin interacting protein M [Source:HGNC Symbol;Acc:HGNC:18417]","synonyms":"HIP17,CXorf27","biotype":"protein_coding","ncbi_id":"25763","summary":"This gene encodes a protein shown to interact with huntingtin, which contains an expanded polyglutamine tract in individuals with Huntington's disease (PMID: 9700202). [provided by RefSeq, Aug 2011]","start":37990817,"end":37991317,"strand":1,"description":"huntingtin interacting protein M [Source:HGNC Symbol;Acc:HGNC:18417]"}, {"versioned_ensembl_gene_id":"ENSG00000232212.1","gene_symbol":"LINC01701","gene_name":"long intergenic non-protein coding RNA 1701 [Source:HGNC Symbol;Acc:HGNC:52489]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985456","summary":null,"start":189775465,"end":189814918,"strand":1,"description":"long intergenic non-protein coding RNA 1701 [Source:HGNC Symbol;Acc:HGNC:52489]"}, {"versioned_ensembl_gene_id":"ENSG00000094914.12","gene_symbol":"AAAS","gene_name":"aladin WD repeat nucleoporin [Source:HGNC Symbol;Acc:HGNC:13666]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8086","summary":"The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":53307456,"end":53324864,"strand":-1,"description":"aladin WD repeat nucleoporin [Source:HGNC Symbol;Acc:HGNC:13666]"}, {"versioned_ensembl_gene_id":"ENSG00000275026.1","gene_symbol":"GXYLT1P4","gene_name":"glucoside xylosyltransferase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50423]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100132441","summary":null,"start":66022661,"end":66027719,"strand":-1,"description":"glucoside xylosyltransferase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50423]"}, {"versioned_ensembl_gene_id":"ENSG00000240950.1","gene_symbol":"AC021074.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142827096,"end":142827728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255395.1","gene_symbol":"AP001972.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75099172,"end":75140148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126838.9","gene_symbol":"PZP","gene_name":"PZP, alpha-2-macroglobulin like [Source:HGNC Symbol;Acc:HGNC:9750]","synonyms":"CPAMD6","biotype":"protein_coding","ncbi_id":"5858","summary":"The protein encoded by this gene is highly expressed in late-pregnancy serum and is similar in structure to alpha-2-macroglobulin. The encoded protein, which acts as a homotetramer, inhibits the activity of all four classes of proteinases. This protein contains cleavage sites for several proteinases. Upon binding of a proteinase, the conformation of this protein changes to trap the proteinase, limiting its activity. This protein appears to be elevated in the sera of presymptomatic Alzheimer's disease patients. [provided by RefSeq, Dec 2016]","start":9148840,"end":9208370,"strand":-1,"description":"PZP, alpha-2-macroglobulin like [Source:HGNC Symbol;Acc:HGNC:9750]"}, {"versioned_ensembl_gene_id":"ENSG00000171570.10","gene_symbol":"RAB4B-EGLN2","gene_name":"RAB4B-EGLN2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44465]","synonyms":"RERT-lncRNA","biotype":"protein_coding","ncbi_id":"100529264","summary":"This locus represents naturally occurring read-through transcription between the neighboring RAB4B (RAB4B, member RAS oncogene family) and EGLN2 (egl nine homolog 2) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":40778242,"end":40808198,"strand":1,"description":"RAB4B-EGLN2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44465]"}, {"versioned_ensembl_gene_id":"ENSG00000161277.10","gene_symbol":"THAP8","gene_name":"THAP domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23191]","synonyms":"FLJ32891","biotype":"protein_coding","ncbi_id":"199745","summary":null,"start":36034985,"end":36054762,"strand":-1,"description":"THAP domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23191]"}, {"versioned_ensembl_gene_id":"ENSG00000036473.6","gene_symbol":"OTC","gene_name":"ornithine carbamoyltransferase [Source:HGNC Symbol;Acc:HGNC:8512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5009","summary":"This nuclear gene encodes a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. Since the gene for this enzyme maps close to that for Duchenne muscular dystrophy, it may play a role in that disease also. [provided by RefSeq, Jul 2008]","start":38352545,"end":38421450,"strand":1,"description":"ornithine carbamoyltransferase [Source:HGNC Symbol;Acc:HGNC:8512]"}, {"versioned_ensembl_gene_id":"ENSG00000169900.7","gene_symbol":"PYDC1","gene_name":"pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30261]","synonyms":"POP1,ASC2","biotype":"protein_coding","ncbi_id":"260434","summary":null,"start":31215962,"end":31217359,"strand":-1,"description":"pyrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30261]"}, {"versioned_ensembl_gene_id":"ENSG00000240454.1","gene_symbol":"AC013828.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13685499,"end":13685656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198077.10","gene_symbol":"CYP2A7","gene_name":"cytochrome P450 family 2 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:2611]","synonyms":"CYP2A","biotype":"protein_coding","ncbi_id":"1549","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum; its substrate has not yet been determined. This gene, which produces two transcript variants, is part of a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. [provided by RefSeq, Jul 2008]","start":40875439,"end":40882752,"strand":-1,"description":"cytochrome P450 family 2 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:2611]"}, {"versioned_ensembl_gene_id":"ENSG00000282020.1","gene_symbol":"AF188030.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1604655,"end":1622707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230749.4","gene_symbol":"MEIS1-AS2","gene_name":"MEIS1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40370]","synonyms":"MEIS1-AS1","biotype":"antisense_RNA","ncbi_id":"100873998","summary":null,"start":66439088,"end":66441836,"strand":-1,"description":"MEIS1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40370]"}, {"versioned_ensembl_gene_id":"ENSG00000241104.5","gene_symbol":"CEACAMP10","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:1822]","synonyms":"CGM17","biotype":"transcribed_processed_pseudogene","ncbi_id":"1098","summary":null,"start":43211791,"end":43248646,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:1822]"}, {"versioned_ensembl_gene_id":"ENSG00000168758.10","gene_symbol":"SEMA4C","gene_name":"semaphorin 4C [Source:HGNC Symbol;Acc:HGNC:10731]","synonyms":"SEMAI,Semaf,Semacl1","biotype":"protein_coding","ncbi_id":"54910","summary":null,"start":96859716,"end":96870757,"strand":-1,"description":"semaphorin 4C [Source:HGNC Symbol;Acc:HGNC:10731]"}, {"versioned_ensembl_gene_id":"ENSG00000038210.12","gene_symbol":"PI4K2B","gene_name":"phosphatidylinositol 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:18215]","synonyms":"PIK42B,PI4KIIB,FLJ11105","biotype":"protein_coding","ncbi_id":"55300","summary":"This gene encodes a member of the type II PI4 kinase protein family. The encoded protein is primarily cytosolic and contributes to overall PI4-kinase activity along with other protein family members. This protein is involved in early T cell activation. [provided by RefSeq, Dec 2016]","start":25233975,"end":25279092,"strand":1,"description":"phosphatidylinositol 4-kinase type 2 beta [Source:HGNC Symbol;Acc:HGNC:18215]"}, {"versioned_ensembl_gene_id":"ENSG00000211826.1","gene_symbol":"TRDJ4","gene_name":"T-cell receptor delta joining 4 [Source:HGNC Symbol;Acc:HGNC:12260]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28519","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22455249,"end":22455296,"strand":1,"description":"T-cell receptor delta joining 4 [Source:HGNC Symbol;Acc:HGNC:12260]"}, {"versioned_ensembl_gene_id":"ENSG00000230136.2","gene_symbol":"BX927132.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181492,"end":29182427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233810.1","gene_symbol":"MOB1AP2","gene_name":"MOB kinase activator 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42639]","synonyms":"MOBKL1BP2","biotype":"processed_pseudogene","ncbi_id":"100873854","summary":null,"start":37291168,"end":37292227,"strand":1,"description":"MOB kinase activator 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42639]"}, {"versioned_ensembl_gene_id":"ENSG00000224832.1","gene_symbol":"LINC01689","gene_name":"long intergenic non-protein coding RNA 1689 [Source:HGNC Symbol;Acc:HGNC:52476]","synonyms":"AP000469.2","biotype":"lincRNA","ncbi_id":"101927869","summary":null,"start":24304550,"end":24321377,"strand":-1,"description":"long intergenic non-protein coding RNA 1689 [Source:HGNC Symbol;Acc:HGNC:52476]"}, {"versioned_ensembl_gene_id":"ENSG00000243621.1","gene_symbol":"AC003989.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111394875,"end":111395043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280359.1","gene_symbol":"AC105133.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77784610,"end":77785070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254458.1","gene_symbol":"AP001107.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66312853,"end":66319237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258425.1","gene_symbol":"AC013451.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74552181,"end":74560048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236346.8","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"NFKBIL,IKBL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31537619,"end":31549575,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000271036.1","gene_symbol":"CLPTM1LP1","gene_name":"CLPTM1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480241","summary":null,"start":189035961,"end":189036444,"strand":-1,"description":"CLPTM1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49023]"}, {"versioned_ensembl_gene_id":"ENSG00000240359.1","gene_symbol":"UBL5P3","gene_name":"ubiquitin like 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44641]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129031","summary":null,"start":63203218,"end":63203448,"strand":-1,"description":"ubiquitin like 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44641]"}, {"versioned_ensembl_gene_id":"ENSG00000143801.16","gene_symbol":"PSEN2","gene_name":"presenilin 2 [Source:HGNC Symbol;Acc:HGNC:9509]","synonyms":"STM2,PS2,AD4,AD3L","biotype":"protein_coding","ncbi_id":"5664","summary":"Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1 or PSEN2) or the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor such that, they either directly regulate gamma-secretase activity, or themselves act are protease enzymes. Two alternatively spliced transcript variants encoding different isoforms of PSEN2 have been identified. [provided by RefSeq, Jul 2008]","start":226870184,"end":226896105,"strand":1,"description":"presenilin 2 [Source:HGNC Symbol;Acc:HGNC:9509]"}, {"versioned_ensembl_gene_id":"ENSG00000075975.15","gene_symbol":"MKRN2","gene_name":"makorin ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:7113]","synonyms":"RNF62,HSPC070","biotype":"protein_coding","ncbi_id":"23609","summary":"This gene encodes a probable E3 ubiquitin ligase containing several zinc finger domains, that is a member of the makorin RING zinc-finger protein family. This gene overlaps the v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1) gene in an antisense orientation and may have a co-regulatory function with RAF1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":12557014,"end":12583713,"strand":1,"description":"makorin ring finger protein 2 [Source:HGNC Symbol;Acc:HGNC:7113]"}, {"versioned_ensembl_gene_id":"ENSG00000254580.1","gene_symbol":"AP001001.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106112459,"end":106132116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230302.2","gene_symbol":"MTND3P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42144]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873181","summary":null,"start":101793454,"end":101793756,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42144]"}, {"versioned_ensembl_gene_id":"ENSG00000233086.7","gene_symbol":"AL358975.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79505804,"end":79532342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258624.1","gene_symbol":"SERPINE4P","gene_name":"serpin family E member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44400]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101930745","summary":null,"start":27340524,"end":27340804,"strand":1,"description":"serpin family E member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:44400]"}, {"versioned_ensembl_gene_id":"ENSG00000157617.16","gene_symbol":"C2CD2","gene_name":"C2 calcium dependent domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1266]","synonyms":"TMEM24L,DKFZP586F0422,C21orf258,C21orf25","biotype":"protein_coding","ncbi_id":"25966","summary":null,"start":41885112,"end":41953890,"strand":-1,"description":"C2 calcium dependent domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1266]"}, {"versioned_ensembl_gene_id":"ENSG00000249274.1","gene_symbol":"PDLIM1P4","gene_name":"PDZ and LIM domain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48947]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419185","summary":null,"start":98782188,"end":98783193,"strand":1,"description":"PDZ and LIM domain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48947]"}, {"versioned_ensembl_gene_id":"ENSG00000221887.5","gene_symbol":"HMSD","gene_name":"histocompatibility minor serpin domain containing [Source:HGNC Symbol;Acc:HGNC:23037]","synonyms":"C18orf53,ACC6,ACC-6","biotype":"protein_coding","ncbi_id":"284293","summary":"This gene encodes a serpin-domain containing protein that may function as a serine protease inhibitor. This gene is primarily expressed in cells of myeloid lineage. A polymorphism in this gene may result in the expression a splice variant that encodes a minor histocompatibility antigen. [provided by RefSeq, Oct 2010]","start":63949301,"end":63981774,"strand":1,"description":"histocompatibility minor serpin domain containing [Source:HGNC Symbol;Acc:HGNC:23037]"}, {"versioned_ensembl_gene_id":"ENSG00000258159.1","gene_symbol":"IMMP1LP2","gene_name":"inner mitochondrial membrane peptidase subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51132]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105369987","summary":null,"start":113015607,"end":113016098,"strand":1,"description":"inner mitochondrial membrane peptidase subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51132]"}, {"versioned_ensembl_gene_id":"ENSG00000238183.2","gene_symbol":"RPS27P5","gene_name":"ribosomal protein S27 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271116","summary":null,"start":226781501,"end":226781744,"strand":1,"description":"ribosomal protein S27 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36734]"}, {"versioned_ensembl_gene_id":"ENSG00000229706.4","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"Em:AC006046.3,PPIP9","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31595839,"end":31596650,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000178096.8","gene_symbol":"BOLA1","gene_name":"bolA family member 1 [Source:HGNC Symbol;Acc:HGNC:24263]","synonyms":"CGI-143","biotype":"protein_coding","ncbi_id":"51027","summary":null,"start":149887890,"end":149900798,"strand":1,"description":"bolA family member 1 [Source:HGNC Symbol;Acc:HGNC:24263]"}, {"versioned_ensembl_gene_id":"ENSG00000282181.1","gene_symbol":"MROH5","gene_name":"maestro heat like repeat family member 5 [Source:HGNC Symbol;Acc:HGNC:42976]","synonyms":"FLJ43860","biotype":"polymorphic_pseudogene","ncbi_id":"389690","summary":null,"start":141439731,"end":141455651,"strand":-1,"description":"maestro heat like repeat family member 5 [Source:HGNC Symbol;Acc:HGNC:42976]"}, {"versioned_ensembl_gene_id":"ENSG00000232194.1","gene_symbol":"Z99943.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167820406,"end":167821224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249372.1","gene_symbol":"ATP6V1G1P6","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37673]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462732","summary":null,"start":78222184,"end":78222517,"strand":1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37673]"}, {"versioned_ensembl_gene_id":"ENSG00000108448.21","gene_symbol":"TRIM16L","gene_name":"tripartite motif containing 16 like [Source:HGNC Symbol;Acc:HGNC:32670]","synonyms":"TRIM70","biotype":"protein_coding","ncbi_id":"147166","summary":null,"start":18697998,"end":18736118,"strand":1,"description":"tripartite motif containing 16 like [Source:HGNC Symbol;Acc:HGNC:32670]"}, {"versioned_ensembl_gene_id":"ENSG00000257556.1","gene_symbol":"LINC02298","gene_name":"long intergenic non-protein coding RNA 2298 [Source:HGNC Symbol;Acc:HGNC:53216]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723354","summary":null,"start":105093609,"end":105099004,"strand":1,"description":"long intergenic non-protein coding RNA 2298 [Source:HGNC Symbol;Acc:HGNC:53216]"}, {"versioned_ensembl_gene_id":"ENSG00000105497.7","gene_symbol":"ZNF175","gene_name":"zinc finger protein 175 [Source:HGNC Symbol;Acc:HGNC:12964]","synonyms":"OTK18","biotype":"protein_coding","ncbi_id":"7728","summary":null,"start":51571298,"end":51592508,"strand":1,"description":"zinc finger protein 175 [Source:HGNC Symbol;Acc:HGNC:12964]"}, {"versioned_ensembl_gene_id":"ENSG00000275178.1","gene_symbol":"AC018529.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77093086,"end":77093446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223847.1","gene_symbol":"AL645474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187714243,"end":187714735,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118939.17","gene_symbol":"UCHL3","gene_name":"ubiquitin C-terminal hydrolase L3 [Source:HGNC Symbol;Acc:HGNC:12515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7347","summary":"The protein encoded by this gene is a member of the deubiquitinating enzyme family. Members of this family are proteases that catalyze the removal of ubiquitin from polypeptides and are divided into five classes, depending on the mechanism of catalysis. This protein may hydrolyze the ubiquitinyl-N-epsilon amide bond of ubiquitinated proteins to regenerate ubiquitin for another catalytic cycle. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":75549480,"end":75606020,"strand":1,"description":"ubiquitin C-terminal hydrolase L3 [Source:HGNC Symbol;Acc:HGNC:12515]"}, {"versioned_ensembl_gene_id":"ENSG00000177971.8","gene_symbol":"IMP3","gene_name":"IMP3, U3 small nucleolar ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14497]","synonyms":"MRPS4,FLJ10968,C15orf12,BRMS2","biotype":"protein_coding","ncbi_id":"55272","summary":"This gene encodes the human homolog of the yeast Imp3 protein. The protein localizes to the nucleoli and interacts with the U3 snoRNP complex. The protein contains an S4 domain. [provided by RefSeq, Jul 2008]","start":75639085,"end":75648706,"strand":-1,"description":"IMP3, U3 small nucleolar ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14497]"}, {"versioned_ensembl_gene_id":"ENSG00000014164.6","gene_symbol":"ZC3H3","gene_name":"zinc finger CCCH-type containing 3 [Source:HGNC Symbol;Acc:HGNC:28972]","synonyms":"ZC3HDC3,KIAA0150","biotype":"protein_coding","ncbi_id":"23144","summary":null,"start":143437655,"end":143541453,"strand":-1,"description":"zinc finger CCCH-type containing 3 [Source:HGNC Symbol;Acc:HGNC:28972]"}, {"versioned_ensembl_gene_id":"ENSG00000152193.7","gene_symbol":"RNF219","gene_name":"ring finger protein 219 [Source:HGNC Symbol;Acc:HGNC:20308]","synonyms":"FLJ13449,C13orf7","biotype":"protein_coding","ncbi_id":"79596","summary":null,"start":78614291,"end":78659179,"strand":-1,"description":"ring finger protein 219 [Source:HGNC Symbol;Acc:HGNC:20308]"}, {"versioned_ensembl_gene_id":"ENSG00000226508.1","gene_symbol":"LINC01918","gene_name":"long intergenic non-protein coding RNA 1918 [Source:HGNC Symbol;Acc:HGNC:52737]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373984","summary":null,"start":105144113,"end":105145424,"strand":1,"description":"long intergenic non-protein coding RNA 1918 [Source:HGNC Symbol;Acc:HGNC:52737]"}, {"versioned_ensembl_gene_id":"ENSG00000165490.12","gene_symbol":"DDIAS","gene_name":"DNA damage induced apoptosis suppressor [Source:HGNC Symbol;Acc:HGNC:26351]","synonyms":"FLJ25416,C11orf82,noxin,FLJ38838","biotype":"protein_coding","ncbi_id":"220042","summary":null,"start":82899975,"end":82958277,"strand":1,"description":"DNA damage induced apoptosis suppressor [Source:HGNC Symbol;Acc:HGNC:26351]"}, {"versioned_ensembl_gene_id":"ENSG00000254441.1","gene_symbol":"AP001646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82835509,"end":82837222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248242.1","gene_symbol":"AC004053.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104653874,"end":104966793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181541.5","gene_symbol":"MAB21L2","gene_name":"mab-21 like 2 [Source:HGNC Symbol;Acc:HGNC:6758]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10586","summary":"This gene is similar to the C. elegans MAB-21 cell fate-determining gene, a downstream target of transforming growth factor-beta signaling. It is thought that this gene may be involved in neural development. The protein encoded by this gene is primarily nuclear, although some cytoplasmic localization has been observed. [provided by RefSeq, Jul 2008]","start":150581922,"end":150584693,"strand":1,"description":"mab-21 like 2 [Source:HGNC Symbol;Acc:HGNC:6758]"}, {"versioned_ensembl_gene_id":"ENSG00000276740.1","gene_symbol":"AL445649.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":107465984,"end":107466674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268957.1","gene_symbol":"AC020914.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51468360,"end":51468636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276887.4","gene_symbol":"TTYH1","gene_name":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57348","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-independent, volume-sensitive large conductance chloride(-) channel. Three transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jan 2011]","start":54345546,"end":54367221,"strand":1,"description":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]"}, {"versioned_ensembl_gene_id":"ENSG00000113916.17","gene_symbol":"BCL6","gene_name":"B-cell CLL/lymphoma 6 [Source:HGNC Symbol;Acc:HGNC:1001]","synonyms":"ZNF51,ZBTB27,LAZ3,BCL6A,BCL5","biotype":"protein_coding","ncbi_id":"604","summary":"The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal POZ domain. This protein acts as a sequence-specific repressor of transcription, and has been shown to modulate the transcription of STAT-dependent IL-4 responses of B cells. This protein can interact with a variety of POZ-containing proteins that function as transcription corepressors. This gene is found to be frequently translocated and hypermutated in diffuse large-cell lymphoma (DLCL), and may be involved in the pathogenesis of DLCL. Alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":187721377,"end":187745727,"strand":-1,"description":"B-cell CLL/lymphoma 6 [Source:HGNC Symbol;Acc:HGNC:1001]"}, {"versioned_ensembl_gene_id":"ENSG00000112079.8","gene_symbol":"STK38","gene_name":"serine/threonine kinase 38 [Source:HGNC Symbol;Acc:HGNC:17847]","synonyms":"NDR","biotype":"protein_coding","ncbi_id":"11329","summary":"This gene encodes a member of the AGC serine/threonine kinase family of proteins. The kinase activity of this protein is regulated by autophosphorylation and phosphorylation by other upstream kinases. This protein has been shown to function in the cell cycle and apoptosis. This protein has also been found to regulate the protein stability and transcriptional activity of the MYC oncogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":36493892,"end":36547470,"strand":-1,"description":"serine/threonine kinase 38 [Source:HGNC Symbol;Acc:HGNC:17847]"}, {"versioned_ensembl_gene_id":"ENSG00000102996.4","gene_symbol":"MMP15","gene_name":"matrix metallopeptidase 15 [Source:HGNC Symbol;Acc:HGNC:7161]","synonyms":"SMCP-2,MTMMP2,MT2-MMP","biotype":"protein_coding","ncbi_id":"4324","summary":"This gene encodes a member of the peptidase M10 family and membrane-type subfamily of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Members of this subfamily contain a transmembrane domain suggesting that these proteins are expressed at the cell surface rather than secreted. The encoded preproprotein is proteolytically processed to generate the mature protease. This protein may play a role in cancer progression. [provided by RefSeq, Jan 2016]","start":58025566,"end":58046901,"strand":1,"description":"matrix metallopeptidase 15 [Source:HGNC Symbol;Acc:HGNC:7161]"}, {"versioned_ensembl_gene_id":"ENSG00000151923.17","gene_symbol":"TIAL1","gene_name":"TIA1 cytotoxic granule associated RNA binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:11804]","synonyms":"TIAR","biotype":"protein_coding","ncbi_id":"7073","summary":"The protein encoded by this gene is a member of a family of RNA-binding proteins, has three RNA recognition motifs (RRMs), and binds adenine and uridine-rich elements in mRNA and pre-mRNAs of a wide range of genes. It regulates various activities including translational control, splicing and apoptosis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. The different isoforms have been show to function differently with respect to post-transcriptional silencing. [provided by RefSeq, Jul 2008]","start":119571802,"end":119597029,"strand":-1,"description":"TIA1 cytotoxic granule associated RNA binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:11804]"}, {"versioned_ensembl_gene_id":"ENSG00000258811.1","gene_symbol":"AL583810.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104842663,"end":104845916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258768.2","gene_symbol":"AL356019.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20260480,"end":20264308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239805.1","gene_symbol":"AC007547.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181847526,"end":181847885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261491.1","gene_symbol":"DNM1P31","gene_name":"dynamin 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35178]","synonyms":"DNM1DN4@,DNM1DN4-2","biotype":"unprocessed_pseudogene","ncbi_id":"644153","summary":null,"start":32384937,"end":32387484,"strand":1,"description":"dynamin 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35178]"}, {"versioned_ensembl_gene_id":"ENSG00000131634.13","gene_symbol":"TMEM204","gene_name":"transmembrane protein 204 [Source:HGNC Symbol;Acc:HGNC:14158]","synonyms":"FLJ20898,CLP24,C16orf30","biotype":"protein_coding","ncbi_id":"79652","summary":"C16ORF30 plays a role in cell adhesion and cellular permeability at adherens junctions (Kearsey et al., 2004 [PubMed 15206924]).[supplied by OMIM, Mar 2008]","start":1528688,"end":1555580,"strand":1,"description":"transmembrane protein 204 [Source:HGNC Symbol;Acc:HGNC:14158]"}, {"versioned_ensembl_gene_id":"ENSG00000005020.12","gene_symbol":"SKAP2","gene_name":"src kinase associated phosphoprotein 2 [Source:HGNC Symbol;Acc:HGNC:15687]","synonyms":"SKAP55R,SKAP-HOM,SCAP2,SAPS,RA70","biotype":"protein_coding","ncbi_id":"8935","summary":"The protein encoded by this gene shares homology with Src kinase-associated phosphoprotein 1, and is a substrate of Src family kinases. It is an adaptor protein that is thought to play an essential role in the Src signaling pathway, and in regulating proper activation of the immune system. This protein contains an amino terminal coiled-coil domain for self-dimerization, a plecskstrin homology (PH) domain required for interactions with lipids at the membrane, and a Src homology (SH3) domain at the carboxy terminus. Some reports indicate that this protein inhibits actin polymerization through interactions with actin assembly factors, and might negatively regulate the invasiveness of tumors by modulating actin assembly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2015]","start":26667062,"end":26995239,"strand":-1,"description":"src kinase associated phosphoprotein 2 [Source:HGNC Symbol;Acc:HGNC:15687]"}, {"versioned_ensembl_gene_id":"ENSG00000248601.1","gene_symbol":"AC116634.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167946674,"end":168113331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184856.6","gene_symbol":"LINC00308","gene_name":"long intergenic non-protein coding RNA 308 [Source:HGNC Symbol;Acc:HGNC:16023]","synonyms":"NCRNA00308,C21orf74,PRED16,NCRNA00308,C21orf74,PRED16","biotype":"lincRNA","ncbi_id":"54143","summary":null,"start":22098617,"end":22116528,"strand":1,"description":"long intergenic non-protein coding RNA 308 [Source:HGNC Symbol;Acc:HGNC:16023]"}, {"versioned_ensembl_gene_id":"ENSG00000164651.16","gene_symbol":"SP8","gene_name":"Sp8 transcription factor [Source:HGNC Symbol;Acc:HGNC:19196]","synonyms":null,"biotype":"protein_coding","ncbi_id":"221833","summary":"The protein encoded by this gene is an SP family transcription factor that in mouse has been shown to be essential for proper limb development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":20782283,"end":20786886,"strand":-1,"description":"Sp8 transcription factor [Source:HGNC Symbol;Acc:HGNC:19196]"}, {"versioned_ensembl_gene_id":"ENSG00000189164.14","gene_symbol":"ZNF527","gene_name":"zinc finger protein 527 [Source:HGNC Symbol;Acc:HGNC:29385]","synonyms":"KIAA1829","biotype":"protein_coding","ncbi_id":"84503","summary":null,"start":37371061,"end":37393066,"strand":1,"description":"zinc finger protein 527 [Source:HGNC Symbol;Acc:HGNC:29385]"}, {"versioned_ensembl_gene_id":"ENSG00000214533.3","gene_symbol":"KRT18P33","gene_name":"keratin 18 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:33402]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647162","summary":null,"start":65666695,"end":65667737,"strand":1,"description":"keratin 18 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:33402]"}, {"versioned_ensembl_gene_id":"ENSG00000186862.17","gene_symbol":"PDZD7","gene_name":"PDZ domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26257]","synonyms":"PDZK7,FLJ23209,DFNB57,bA108L7.8","biotype":"protein_coding","ncbi_id":"79955","summary":"This gene encodes a ciliary protein homologous to proteins which are mutated in Usher syndrome patients, and mutations and translocations involving this gene have been associated with two types of Usher syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":101007683,"end":101031157,"strand":-1,"description":"PDZ domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26257]"}, {"versioned_ensembl_gene_id":"ENSG00000239261.1","gene_symbol":"RPL31P41","gene_name":"ribosomal protein L31 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271201","summary":null,"start":65155407,"end":65155778,"strand":1,"description":"ribosomal protein L31 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36720]"}, {"versioned_ensembl_gene_id":"ENSG00000280725.1","gene_symbol":"LINC00251","gene_name":"long intergenic non-protein coding RNA 251 [Source:HGNC Symbol;Acc:HGNC:31950]","synonyms":"NCRNA00251,C8orf25","biotype":"lincRNA","ncbi_id":"552859","summary":null,"start":65161145,"end":65180341,"strand":-1,"description":"long intergenic non-protein coding RNA 251 [Source:HGNC Symbol;Acc:HGNC:31950]"}, {"versioned_ensembl_gene_id":"ENSG00000232358.1","gene_symbol":"AL050404.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50999370,"end":51010019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248920.2","gene_symbol":"USP17L19","gene_name":"ubiquitin specific peptidase 17-like family member 19 [Source:HGNC Symbol;Acc:HGNC:44447]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287404","summary":null,"start":9253378,"end":9255329,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 19 [Source:HGNC Symbol;Acc:HGNC:44447]"}, {"versioned_ensembl_gene_id":"ENSG00000138617.14","gene_symbol":"PARP16","gene_name":"poly(ADP-ribose) polymerase family member 16 [Source:HGNC Symbol;Acc:HGNC:26040]","synonyms":"pART15,FLJ25281,FLJ20509,C15orf30","biotype":"protein_coding","ncbi_id":"54956","summary":null,"start":65234460,"end":65300618,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 16 [Source:HGNC Symbol;Acc:HGNC:26040]"}, {"versioned_ensembl_gene_id":"ENSG00000242307.1","gene_symbol":"AC010401.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13922332,"end":13922679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172199.1","gene_symbol":"OR8U1","gene_name":"olfactory receptor family 8 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:19611]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219417","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56375624,"end":56376553,"strand":1,"description":"olfactory receptor family 8 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:19611]"}, {"versioned_ensembl_gene_id":"ENSG00000109606.12","gene_symbol":"DHX15","gene_name":"DEAH-box helicase 15 [Source:HGNC Symbol;Acc:HGNC:2738]","synonyms":"DDX15,DBP1,PrPp43p,PRPF43,PRP43,HRH2","biotype":"protein_coding","ncbi_id":"1665","summary":"The protein encoded by this gene is a putative ATP-dependent RNA helicase implicated in pre-mRNA splicing. [provided by RefSeq, Jul 2008]","start":24517441,"end":24584550,"strand":-1,"description":"DEAH-box helicase 15 [Source:HGNC Symbol;Acc:HGNC:2738]"}, {"versioned_ensembl_gene_id":"ENSG00000136490.8","gene_symbol":"LIMD2","gene_name":"LIM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28142]","synonyms":"MGC10986","biotype":"protein_coding","ncbi_id":"80774","summary":null,"start":63695902,"end":63701172,"strand":-1,"description":"LIM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28142]"}, {"versioned_ensembl_gene_id":"ENSG00000138778.11","gene_symbol":"CENPE","gene_name":"centromere protein E [Source:HGNC Symbol;Acc:HGNC:1856]","synonyms":"PPP1R61,KIF10","biotype":"protein_coding","ncbi_id":"1062","summary":"Centrosome-associated protein E (CENPE) is a kinesin-like motor protein that accumulates in the G2 phase of the cell cycle. Unlike other centrosome-associated proteins, it is not present during interphase and first appears at the centromere region of chromosomes during prometaphase. This protein is required for stable spindle microtubule capture at kinetochores which is a necessary step in chromosome alignment during prometaphase. This protein also couples chromosome position to microtubule depolymerizing activity. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Nov 2014]","start":103105806,"end":103198409,"strand":-1,"description":"centromere protein E [Source:HGNC Symbol;Acc:HGNC:1856]"}, {"versioned_ensembl_gene_id":"ENSG00000278812.2","gene_symbol":"C8orf31","gene_name":"chromosome 8 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26731]","synonyms":"FLJ37131","biotype":"processed_transcript","ncbi_id":"286122","summary":null,"start":143039209,"end":143059942,"strand":1,"description":"chromosome 8 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26731]"}, {"versioned_ensembl_gene_id":"ENSG00000171505.5","gene_symbol":"OR1N1","gene_name":"olfactory receptor family 1 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:8221]","synonyms":"OR1N3,OR1-26","biotype":"protein_coding","ncbi_id":"138883","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122526358,"end":122527296,"strand":-1,"description":"olfactory receptor family 1 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:8221]"}, {"versioned_ensembl_gene_id":"ENSG00000235435.1","gene_symbol":"AC096666.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145294277,"end":145331847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136834.3","gene_symbol":"OR1J1","gene_name":"olfactory receptor family 1 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:8208]","synonyms":"hg32","biotype":"protein_coding","ncbi_id":"347168","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122476958,"end":122477926,"strand":-1,"description":"olfactory receptor family 1 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:8208]"}, {"versioned_ensembl_gene_id":"ENSG00000184566.3","gene_symbol":"AC132216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33880643,"end":33881800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271848.1","gene_symbol":"AC073389.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73654039,"end":73674719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233616.2","gene_symbol":"AL359636.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122400970,"end":122402906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107902.13","gene_symbol":"LHPP","gene_name":"phospholysine phosphohistidine inorganic pyrophosphate phosphatase [Source:HGNC Symbol;Acc:HGNC:30042]","synonyms":"HDHD2B","biotype":"protein_coding","ncbi_id":"64077","summary":null,"start":124461834,"end":124617888,"strand":1,"description":"phospholysine phosphohistidine inorganic pyrophosphate phosphatase [Source:HGNC Symbol;Acc:HGNC:30042]"}, {"versioned_ensembl_gene_id":"ENSG00000203995.9","gene_symbol":"ZYG11A","gene_name":"zyg-11 family member A, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:32058]","synonyms":"ZYG11","biotype":"protein_coding","ncbi_id":"440590","summary":null,"start":52842511,"end":52894998,"strand":1,"description":"zyg-11 family member A, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:32058]"}, {"versioned_ensembl_gene_id":"ENSG00000118523.5","gene_symbol":"CTGF","gene_name":"connective tissue growth factor [Source:HGNC Symbol;Acc:HGNC:2500]","synonyms":"IGFBP8,CCN2","biotype":"protein_coding","ncbi_id":"1490","summary":"The protein encoded by this gene is a mitogen that is secreted by vascular endothelial cells. The encoded protein plays a role in chondrocyte proliferation and differentiation, cell adhesion in many cell types, and is related to platelet-derived growth factor. Certain polymorphisms in this gene have been linked with a higher incidence of systemic sclerosis. [provided by RefSeq, Nov 2009]","start":131948176,"end":131951373,"strand":-1,"description":"connective tissue growth factor [Source:HGNC Symbol;Acc:HGNC:2500]"}, {"versioned_ensembl_gene_id":"ENSG00000227220.1","gene_symbol":"AL133346.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131950946,"end":132077393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120963.11","gene_symbol":"ZNF706","gene_name":"zinc finger protein 706 [Source:HGNC Symbol;Acc:HGNC:24992]","synonyms":"HSPC038","biotype":"protein_coding","ncbi_id":"51123","summary":null,"start":101177878,"end":101206193,"strand":-1,"description":"zinc finger protein 706 [Source:HGNC Symbol;Acc:HGNC:24992]"}, {"versioned_ensembl_gene_id":"ENSG00000206279.10","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"protein_coding","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33247394,"end":33258105,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000234781.2","gene_symbol":"LINC01103","gene_name":"long intergenic non-protein coding RNA 1103 [Source:HGNC Symbol;Acc:HGNC:49225]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927360","summary":null,"start":104488458,"end":104510509,"strand":-1,"description":"long intergenic non-protein coding RNA 1103 [Source:HGNC Symbol;Acc:HGNC:49225]"}, {"versioned_ensembl_gene_id":"ENSG00000254031.5","gene_symbol":"AC022858.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71155457,"end":71204223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231960.1","gene_symbol":"BX927132.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29124176,"end":29128873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242288.9","gene_symbol":"AC022400.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73674295,"end":73730466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165409.16","gene_symbol":"TSHR","gene_name":"thyroid stimulating hormone receptor [Source:HGNC Symbol;Acc:HGNC:12373]","synonyms":"LGR3","biotype":"protein_coding","ncbi_id":"7253","summary":"The protein encoded by this gene is a membrane protein and a major controller of thyroid cell metabolism. The encoded protein is a receptor for thyrothropin and thyrostimulin, and its activity is mediated by adenylate cyclase. Defects in this gene are a cause of several types of hyperthyroidism. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":80954989,"end":81146302,"strand":1,"description":"thyroid stimulating hormone receptor [Source:HGNC Symbol;Acc:HGNC:12373]"}, {"versioned_ensembl_gene_id":"ENSG00000185689.15","gene_symbol":"C6orf201","gene_name":"chromosome 6 open reading frame 201 [Source:HGNC Symbol;Acc:HGNC:21620]","synonyms":"dJ1013A10.5","biotype":"protein_coding","ncbi_id":"404220","summary":null,"start":4079209,"end":4130951,"strand":1,"description":"chromosome 6 open reading frame 201 [Source:HGNC Symbol;Acc:HGNC:21620]"}, {"versioned_ensembl_gene_id":"ENSG00000271705.1","gene_symbol":"RPL17P3","gene_name":"ribosomal protein L17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19796]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"326286","summary":null,"start":81001166,"end":81001786,"strand":-1,"description":"ribosomal protein L17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19796]"}, {"versioned_ensembl_gene_id":"ENSG00000276738.1","gene_symbol":"AP001506.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20597953,"end":20598163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006042.11","gene_symbol":"TMEM98","gene_name":"transmembrane protein 98 [Source:HGNC Symbol;Acc:HGNC:24529]","synonyms":"DKFZP564K1964","biotype":"protein_coding","ncbi_id":"26022","summary":"This gene encodes a transmembrane protein. A missense mutation in this gene result in Nanophthalmos 4 (NNO4). Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2014]","start":32927910,"end":32945106,"strand":1,"description":"transmembrane protein 98 [Source:HGNC Symbol;Acc:HGNC:24529]"}, {"versioned_ensembl_gene_id":"ENSG00000102738.7","gene_symbol":"MRPS31","gene_name":"mitochondrial ribosomal protein S31 [Source:HGNC Symbol;Acc:HGNC:16632]","synonyms":"IMOGN38","biotype":"protein_coding","ncbi_id":"10240","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. The 28S subunit of the mammalian mitoribosome may play a crucial and characteristic role in translation initiation. This gene encodes a 28S subunit protein that has also been associated with type 1 diabetes; however, its relationship to the etiology of this disease remains to be clarified. Pseudogenes corresponding to this gene have been found on chromosomes 3 and 13. [provided by RefSeq, Jul 2008]","start":40729135,"end":40771173,"strand":-1,"description":"mitochondrial ribosomal protein S31 [Source:HGNC Symbol;Acc:HGNC:16632]"}, {"versioned_ensembl_gene_id":"ENSG00000263097.3","gene_symbol":"TAS2R31","gene_name":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]","synonyms":"T2R53,T2R31,TAS2R44","biotype":"protein_coding","ncbi_id":"259290","summary":"TAS2R44 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11030387,"end":11031407,"strand":-1,"description":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]"}, {"versioned_ensembl_gene_id":"ENSG00000131368.7","gene_symbol":"MRPS25","gene_name":"mitochondrial ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:14511]","synonyms":"RPMS25,MRP-S25,FLJ00023,DKFZp313H0817","biotype":"protein_coding","ncbi_id":"64432","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. A pseudogene corresponding to this gene is found on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":15042460,"end":15065335,"strand":-1,"description":"mitochondrial ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:14511]"}, {"versioned_ensembl_gene_id":"ENSG00000213463.4","gene_symbol":"SYNJ2BP","gene_name":"synaptojanin 2 binding protein [Source:HGNC Symbol;Acc:HGNC:18955]","synonyms":"Arip2","biotype":"protein_coding","ncbi_id":"55333","summary":null,"start":70366496,"end":70417061,"strand":-1,"description":"synaptojanin 2 binding protein [Source:HGNC Symbol;Acc:HGNC:18955]"}, {"versioned_ensembl_gene_id":"ENSG00000009694.13","gene_symbol":"TENM1","gene_name":"teneurin transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:8117]","synonyms":"TNM,TEN-M1,ODZ3,ODZ1","biotype":"protein_coding","ncbi_id":"10178","summary":"The protein encoded by this gene belongs to the tenascin family and teneurin subfamily. It is expressed in the neurons and may function as a cellular signal transducer. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":124375903,"end":124963817,"strand":-1,"description":"teneurin transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:8117]"}, {"versioned_ensembl_gene_id":"ENSG00000232412.1","gene_symbol":"AL121601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123959233,"end":123961341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234564.1","gene_symbol":"HSPA8P20","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:44936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129231","summary":null,"start":124204499,"end":124205806,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:44936]"}, {"versioned_ensembl_gene_id":"ENSG00000258910.2","gene_symbol":"LINC01956","gene_name":"long intergenic non-protein coding RNA 1956 [Source:HGNC Symbol;Acc:HGNC:52777]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985816","summary":null,"start":118833700,"end":118835110,"strand":-1,"description":"long intergenic non-protein coding RNA 1956 [Source:HGNC Symbol;Acc:HGNC:52777]"}, {"versioned_ensembl_gene_id":"ENSG00000216998.1","gene_symbol":"CYP2AC1P","gene_name":"cytochrome P450 family 2 subfamily AC member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39976]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"106478960","summary":null,"start":49565924,"end":49580166,"strand":-1,"description":"cytochrome P450 family 2 subfamily AC member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39976]"}, {"versioned_ensembl_gene_id":"ENSG00000226893.3","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29879284,"end":29882006,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000244165.1","gene_symbol":"P2RY11","gene_name":"purinergic receptor P2Y11 [Source:HGNC Symbol;Acc:HGNC:8540]","synonyms":"P2Y11","biotype":"protein_coding","ncbi_id":"5032","summary":"The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is coupled to the stimulation of the phosphoinositide and adenylyl cyclase pathways and behaves as a selective purinoceptor. Naturally occuring read-through transcripts, resulting from intergenic splicing between this gene and an immediately upstream gene (PPAN, encoding peter pan homolog), have been found. The PPAN-P2RY11 read-through mRNA is ubiquitously expressed and encodes a fusion protein that shares identity with each individual gene product. [provided by RefSeq, Jul 2008]","start":10111538,"end":10115372,"strand":1,"description":"purinergic receptor P2Y11 [Source:HGNC Symbol;Acc:HGNC:8540]"}, {"versioned_ensembl_gene_id":"ENSG00000226152.1","gene_symbol":"AL671561.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878828,"end":29879794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231309.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31364601,"end":31366055,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000275317.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803627,"end":54814543,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000227956.2","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"bCX67J3.3,bQB90C11.3,HCG4P6,HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29917455,"end":29918445,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000272371.1","gene_symbol":"AL591167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52554818,"end":52555273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260055.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29794107,"end":29796116,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000261279.5","gene_symbol":"ULK4P1","gene_name":"ULK4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15775]","synonyms":"FAM7A1,D-X","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"89838","summary":null,"start":32406597,"end":32434992,"strand":-1,"description":"ULK4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15775]"}, {"versioned_ensembl_gene_id":"ENSG00000233928.5","gene_symbol":"AL591501.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33726508,"end":33942280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226408.1","gene_symbol":"CR759815.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31278735,"end":31280532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130024.14","gene_symbol":"PHF10","gene_name":"PHD finger protein 10 [Source:HGNC Symbol;Acc:HGNC:18250]","synonyms":"XAP135,FLJ10975,BAF45a","biotype":"protein_coding","ncbi_id":"55274","summary":"This gene contains a predicted ORF that encodes a protein with two zinc finger domains. The function of the encoded protein is not known. Sequence analysis suggests that multiple alternatively spliced transcript variants are derived from this gene but the full-length nature of only two of them is known. These two splice variants encode different isoforms. A pseudogene for this gene is located on Xq28. [provided by RefSeq, Jul 2008]","start":169703905,"end":169725566,"strand":-1,"description":"PHD finger protein 10 [Source:HGNC Symbol;Acc:HGNC:18250]"}, {"versioned_ensembl_gene_id":"ENSG00000185127.6","gene_symbol":"C6orf120","gene_name":"chromosome 6 open reading frame 120 [Source:HGNC Symbol;Acc:HGNC:21247]","synonyms":"bA160E12.4","biotype":"protein_coding","ncbi_id":"387263","summary":"This gene encodes a conserved, N-glycosylated protein that likely functions in the cellular response to endoplasmic reticulum stress. This protein is able to induce apoptosis in vitro in CD4+ T-cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":169702190,"end":169704856,"strand":1,"description":"chromosome 6 open reading frame 120 [Source:HGNC Symbol;Acc:HGNC:21247]"}, {"versioned_ensembl_gene_id":"ENSG00000170681.6","gene_symbol":"CAVIN4","gene_name":"caveolae associated protein 4 [Source:HGNC Symbol;Acc:HGNC:33742]","synonyms":"MURC,cavin-4","biotype":"protein_coding","ncbi_id":"347273","summary":"This gene encodes a protein containing two coiled-coil regions. The encoded protein promotes Rho/ROCK (Rho-kinase) signaling in cardiac muscles cells, and may facilitate myofibrillar organization. [provided by RefSeq, Jun 2013]","start":100578079,"end":100587906,"strand":1,"description":"caveolae associated protein 4 [Source:HGNC Symbol;Acc:HGNC:33742]"}, {"versioned_ensembl_gene_id":"ENSG00000267554.1","gene_symbol":"AC015911.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35470069,"end":35470628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196383.6","gene_symbol":"OR4Q2","gene_name":"olfactory receptor family 4 subfamily Q member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15359]","synonyms":"OR4Q2P","biotype":"polymorphic_pseudogene","ncbi_id":"390432","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":19999913,"end":20004760,"strand":1,"description":"olfactory receptor family 4 subfamily Q member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15359]"}, {"versioned_ensembl_gene_id":"ENSG00000182103.4","gene_symbol":"FAM181B","gene_name":"family with sequence similarity 181 member B [Source:HGNC Symbol;Acc:HGNC:28512]","synonyms":"MGC33846,LOC220382","biotype":"protein_coding","ncbi_id":"220382","summary":null,"start":82729941,"end":82733864,"strand":-1,"description":"family with sequence similarity 181 member B [Source:HGNC Symbol;Acc:HGNC:28512]"}, {"versioned_ensembl_gene_id":"ENSG00000106384.10","gene_symbol":"MOGAT3","gene_name":"monoacylglycerol O-acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:23249]","synonyms":"MGAT3,DGAT2L2,DC7","biotype":"protein_coding","ncbi_id":"346606","summary":"Acyl-CoA:monoacylglycerol acyltransferase (MOGAT; EC 2.3.1.22) catalyzes the synthesis of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA (Cheng et al., 2003 [PubMed 12618427]).[supplied by OMIM, Mar 2008]","start":101195007,"end":101201021,"strand":-1,"description":"monoacylglycerol O-acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:23249]"}, {"versioned_ensembl_gene_id":"ENSG00000227097.5","gene_symbol":"RPS28P7","gene_name":"ribosomal protein S28 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35787]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646195","summary":null,"start":82689559,"end":82689768,"strand":1,"description":"ribosomal protein S28 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35787]"}, {"versioned_ensembl_gene_id":"ENSG00000147408.14","gene_symbol":"CSGALNACT1","gene_name":"chondroitin sulfate N-acetylgalactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24290]","synonyms":"FLJ11264,CSGalNAcT-1,ChGn","biotype":"protein_coding","ncbi_id":"55790","summary":"This gene encodes an enzyme that transfers N-acetylglucosamine (GalNAc) to the core tetrasaccharide linker and to elongating chondroitin sulfate chains in proteoglycans. Knockout of the orthologous mouse gene indicates that the protein is necessary for normal cartilage development and aggrecan metabolism. Mutations in this gene are associated with multiple sclerosis progression, and with mild skeletal dysplasia and joint laxity. [provided by RefSeq, Aug 2017]","start":19404161,"end":19758029,"strand":-1,"description":"chondroitin sulfate N-acetylgalactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24290]"}, {"versioned_ensembl_gene_id":"ENSG00000253270.1","gene_symbol":"AC090541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19678572,"end":19688934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174970.4","gene_symbol":"OR10AG1","gene_name":"olfactory receptor family 10 subfamily AG member 1 [Source:HGNC Symbol;Acc:HGNC:19607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282770","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55965755,"end":55969945,"strand":-1,"description":"olfactory receptor family 10 subfamily AG member 1 [Source:HGNC Symbol;Acc:HGNC:19607]"}, {"versioned_ensembl_gene_id":"ENSG00000254747.1","gene_symbol":"MTND4LP18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42252]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075101","summary":null,"start":81552226,"end":81552516,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42252]"}, {"versioned_ensembl_gene_id":"ENSG00000255014.1","gene_symbol":"ARL6IP1P3","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44972]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729790","summary":null,"start":80653429,"end":80653988,"strand":-1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44972]"}, {"versioned_ensembl_gene_id":"ENSG00000277969.1","gene_symbol":"AC006449.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38702452,"end":38704747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258645.2","gene_symbol":"HSPE1P2","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20052]","synonyms":"HSPEP2","biotype":"processed_pseudogene","ncbi_id":"326300","summary":null,"start":63601509,"end":63601814,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20052]"}, {"versioned_ensembl_gene_id":"ENSG00000275665.1","gene_symbol":"AC006449.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38715328,"end":38720272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259784.1","gene_symbol":"AC093525.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2513965,"end":2527955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225680.1","gene_symbol":"AL163953.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53599832,"end":53614026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226132.1","gene_symbol":"RPS3AP46","gene_name":"ribosomal protein S3a pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36338]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271596","summary":null,"start":53612724,"end":53613405,"strand":1,"description":"ribosomal protein S3a pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36338]"}, {"versioned_ensembl_gene_id":"ENSG00000275854.1","gene_symbol":"AC084824.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32736930,"end":32737660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233935.1","gene_symbol":"AL669813.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29716960,"end":29717950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228248.1","gene_symbol":"NUTF2P3","gene_name":"nuclear transport factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50452]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480298","summary":null,"start":77580245,"end":77580628,"strand":1,"description":"nuclear transport factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50452]"}, {"versioned_ensembl_gene_id":"ENSG00000232167.1","gene_symbol":"AC137675.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27525353,"end":27525394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271958.1","gene_symbol":"AC021860.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38618265,"end":38619437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142208.15","gene_symbol":"AKT1","gene_name":"AKT serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:391]","synonyms":"RAC,PRKBA,PKB,AKT","biotype":"protein_coding","ncbi_id":"207","summary":"This gene encodes one of the three members of the human AKT serine-threonine protein kinase family which are often referred to as protein kinase B alpha, beta, and gamma. These highly similar AKT proteins all have an N-terminal pleckstrin homology domain, a serine/threonine-specific kinase domain and a C-terminal regulatory domain. These proteins are phosphorylated by phosphoinositide 3-kinase (PI3K). AKT/PI3K forms a key component of many signalling pathways that involve the binding of membrane-bound ligands such as receptor tyrosine kinases, G-protein coupled receptors, and integrin-linked kinase. These AKT proteins therefore regulate a wide variety of cellular functions including cell proliferation, survival, metabolism, and angiogenesis in both normal and malignant cells. AKT proteins are recruited to the cell membrane by phosphatidylinositol 3,4,5-trisphosphate (PIP3) after phosphorylation of phosphatidylinositol 4,5-bisphosphate (PIP2) by PI3K. Subsequent phosphorylation of both threonine residue 308 and serine residue 473 is required for full activation of the AKT1 protein encoded by this gene. Phosphorylation of additional residues also occurs, for example, in response to insulin growth factor-1 and epidermal growth factor. Protein phosphatases act as negative regulators of AKT proteins by dephosphorylating AKT or PIP3. The PI3K/AKT signalling pathway is crucial for tumor cell survival. Survival factors can suppress apoptosis in a transcription-independent manner by activating AKT1 which then phosphorylates and inactivates components of the apoptotic machinery. AKT proteins also participate in the mammalian target of rapamycin (mTOR) signalling pathway which controls the assembly of the eukaryotic translation initiation factor 4F (eIF4E) complex and this pathway, in addition to responding to extracellular signals from growth factors and cytokines, is disregulated in many cancers. Mutations in this gene are associated with multiple types of cancer and excessive tissue growth including Proteus syndrome and Cowden syndrome 6, and breast, colorectal, and ovarian cancers. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2020]","start":104769349,"end":104795751,"strand":-1,"description":"AKT serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:391]"}, {"versioned_ensembl_gene_id":"ENSG00000282170.1","gene_symbol":"TRY2P","gene_name":"trypsinogen-like pseudogene [Source:NCBI gene;Acc:207147]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"207147","summary":null,"start":142265850,"end":142272254,"strand":-1,"description":"trypsinogen-like pseudogene [Source:NCBI gene;Acc:207147]"}, {"versioned_ensembl_gene_id":"ENSG00000095303.14","gene_symbol":"PTGS1","gene_name":"prostaglandin-endoperoxide synthase 1 [Source:HGNC Symbol;Acc:HGNC:9604]","synonyms":"PTGHS,PGHS-1,COX1","biotype":"protein_coding","ncbi_id":"5742","summary":"This is one of two genes encoding similar enzymes that catalyze the conversion of arachinodate to prostaglandin. The encoded protein regulates angiogenesis in endothelial cells, and is inhibited by nonsteroidal anti-inflammatory drugs such as aspirin. Based on its ability to function as both a cyclooxygenase and as a peroxidase, the encoded protein has been identified as a moonlighting protein. The protein may promote cell proliferation during tumor progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":122370530,"end":122395703,"strand":1,"description":"prostaglandin-endoperoxide synthase 1 [Source:HGNC Symbol;Acc:HGNC:9604]"}, {"versioned_ensembl_gene_id":"ENSG00000250137.1","gene_symbol":"AC093607.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23560923,"end":23768652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215096.3","gene_symbol":"IFITM8P","gene_name":"interferon induced transmembrane protein 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:32202]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"613204","summary":null,"start":63409064,"end":63409457,"strand":1,"description":"interferon induced transmembrane protein 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:32202]"}, {"versioned_ensembl_gene_id":"ENSG00000255516.1","gene_symbol":"AP005436.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88050106,"end":88062110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258679.1","gene_symbol":"AC121758.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":56822985,"end":56874268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218472.2","gene_symbol":"AL590004.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3913922,"end":3914292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143479.15","gene_symbol":"DYRK3","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 3 [Source:HGNC Symbol;Acc:HGNC:3094]","synonyms":"hYAK3-2,REDK,RED","biotype":"protein_coding","ncbi_id":"8444","summary":"This gene product belongs to the DYRK family of dual-specificity protein kinases that catalyze autophosphorylation on serine/threonine and tyrosine residues. The members of this family share structural similarity, however, differ in their substrate specificity, suggesting their involvement in different cellular functions. The encoded protein has been shown to autophosphorylate on tyrosine residue and catalyze phosphorylation of histones H3 and H2B in vitro. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":206635536,"end":206684419,"strand":1,"description":"dual specificity tyrosine phosphorylation regulated kinase 3 [Source:HGNC Symbol;Acc:HGNC:3094]"}, {"versioned_ensembl_gene_id":"ENSG00000241334.2","gene_symbol":"AC099521.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68477237,"end":68477570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237605.1","gene_symbol":"AL591846.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206634649,"end":206635622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274698.1","gene_symbol":"AC099521.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68450283,"end":68452318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136943.10","gene_symbol":"CTSV","gene_name":"cathepsin V [Source:HGNC Symbol;Acc:HGNC:2538]","synonyms":"CTSU,CTSL2","biotype":"protein_coding","ncbi_id":"1515","summary":"The protein encoded by this gene, a member of the peptidase C1 family, is a lysosomal cysteine proteinase that may play an important role in corneal physiology. This gene is expressed in colorectal and breast carcinomas but not in normal colon, mammary gland, or peritumoral tissues, suggesting a possible role for this gene in tumor processes. Alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2011]","start":97029679,"end":97039643,"strand":-1,"description":"cathepsin V [Source:HGNC Symbol;Acc:HGNC:2538]"}, {"versioned_ensembl_gene_id":"ENSG00000260378.1","gene_symbol":"AC109597.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12745873,"end":12757835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248837.5","gene_symbol":"AC097512.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22997551,"end":23056862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280205.1","gene_symbol":"AC009716.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76385642,"end":76389406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263982.1","gene_symbol":"AC009716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76372717,"end":76378275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154760.13","gene_symbol":"SLFN13","gene_name":"schlafen family member 13 [Source:HGNC Symbol;Acc:HGNC:26481]","synonyms":"FLJ31952","biotype":"protein_coding","ncbi_id":"146857","summary":null,"start":35435096,"end":35448837,"strand":-1,"description":"schlafen family member 13 [Source:HGNC Symbol;Acc:HGNC:26481]"}, {"versioned_ensembl_gene_id":"ENSG00000101493.10","gene_symbol":"ZNF516","gene_name":"zinc finger protein 516 [Source:HGNC Symbol;Acc:HGNC:28990]","synonyms":"KIAA0222,HsT287","biotype":"protein_coding","ncbi_id":"9658","summary":"Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc-finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. [provided by RefSeq, Sep 2012]","start":76358190,"end":76495190,"strand":-1,"description":"zinc finger protein 516 [Source:HGNC Symbol;Acc:HGNC:28990]"}, {"versioned_ensembl_gene_id":"ENSG00000115561.15","gene_symbol":"CHMP3","gene_name":"charged multivesicular body protein 3 [Source:HGNC Symbol;Acc:HGNC:29865]","synonyms":"CGI-149,VPS24,NEDF","biotype":"protein_coding","ncbi_id":"51652","summary":"This gene encodes a protein that sorts transmembrane proteins into lysosomes/vacuoles via the multivesicular body (MVB) pathway. This protein, along with other soluble coiled-coil containing proteins, forms part of the ESCRT-III protein complex that binds to the endosomal membrane and recruits additional cofactors for protein sorting into the MVB. This protein may also co-immunoprecipitate with a member of the IFG-binding protein superfamily. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ring finger protein 103 (RNF103) gene. [provided by RefSeq, Nov 2010]","start":86503431,"end":86563479,"strand":-1,"description":"charged multivesicular body protein 3 [Source:HGNC Symbol;Acc:HGNC:29865]"}, {"versioned_ensembl_gene_id":"ENSG00000185019.16","gene_symbol":"UBOX5","gene_name":"U-box domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17777]","synonyms":"UIP5,Ubce7ip5,RNF37,KIAA0860","biotype":"protein_coding","ncbi_id":"22888","summary":"This gene encodes a U-box domain containing protein. The encoded protein interacts with E2 enzymes and may play a role in the ubiquitination pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":3107573,"end":3160196,"strand":-1,"description":"U-box domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17777]"}, {"versioned_ensembl_gene_id":"ENSG00000167011.8","gene_symbol":"NAT16","gene_name":"N-acetyltransferase 16 (putative) [Source:HGNC Symbol;Acc:HGNC:22030]","synonyms":"FLJ39237,C7orf52","biotype":"protein_coding","ncbi_id":"375607","summary":null,"start":101170493,"end":101180276,"strand":-1,"description":"N-acetyltransferase 16 (putative) [Source:HGNC Symbol;Acc:HGNC:22030]"}, {"versioned_ensembl_gene_id":"ENSG00000124228.14","gene_symbol":"DDX27","gene_name":"DEAD-box helicase 27 [Source:HGNC Symbol;Acc:HGNC:15837]","synonyms":"DRS1,dJ686N3.1","biotype":"protein_coding","ncbi_id":"55661","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein involved in the processing of 5.8S and 28S ribosomal RNAs. More specifically, the encoded protein localizes to the nucleolus, where it interacts with the PeBoW complex to ensure proper 3' end formation of 47S rRNA. [provided by RefSeq, Jan 2017]","start":49219295,"end":49244077,"strand":1,"description":"DEAD-box helicase 27 [Source:HGNC Symbol;Acc:HGNC:15837]"}, {"versioned_ensembl_gene_id":"ENSG00000226175.1","gene_symbol":"BX927221.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30231863,"end":30233684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224863.2","gene_symbol":"LINC01398","gene_name":"long intergenic non-protein coding RNA 1398 [Source:HGNC Symbol;Acc:HGNC:50678]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101929651","summary":null,"start":46446673,"end":46451281,"strand":-1,"description":"long intergenic non-protein coding RNA 1398 [Source:HGNC Symbol;Acc:HGNC:50678]"}, {"versioned_ensembl_gene_id":"ENSG00000234178.1","gene_symbol":"DEFA11P","gene_name":"defensin alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:33354]","synonyms":"DEFAP3","biotype":"unprocessed_pseudogene","ncbi_id":"724068","summary":null,"start":7028641,"end":7029489,"strand":-1,"description":"defensin alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:33354]"}, {"versioned_ensembl_gene_id":"ENSG00000122741.15","gene_symbol":"DCAF10","gene_name":"DDB1 and CUL4 associated factor 10 [Source:HGNC Symbol;Acc:HGNC:23686]","synonyms":"MGC10765,FLJ23201,WDR32","biotype":"protein_coding","ncbi_id":"79269","summary":null,"start":37800502,"end":37867666,"strand":1,"description":"DDB1 and CUL4 associated factor 10 [Source:HGNC Symbol;Acc:HGNC:23686]"}, {"versioned_ensembl_gene_id":"ENSG00000238221.1","gene_symbol":"AL139095.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7276031,"end":7298872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138080.13","gene_symbol":"EMILIN1","gene_name":"elastin microfibril interfacer 1 [Source:HGNC Symbol;Acc:HGNC:19880]","synonyms":"gp115,DKFZp586M121","biotype":"protein_coding","ncbi_id":"11117","summary":"This gene encodes an extracellular matrix glycoprotein that is characterized by an N-terminal microfibril interface domain, a coiled-coiled alpha-helical domain, a collagenous domain and a C-terminal globular C1q domain. The encoded protein associates with elastic fibers at the interface between elastin and microfibrils and may play a role in the development of elastic tissues including large blood vessels, dermis, heart and lung. [provided by RefSeq, Sep 2009]","start":27078567,"end":27086408,"strand":1,"description":"elastin microfibril interfacer 1 [Source:HGNC Symbol;Acc:HGNC:19880]"}, {"versioned_ensembl_gene_id":"ENSG00000258056.2","gene_symbol":"AC009779.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55729104,"end":55730852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185728.16","gene_symbol":"YTHDF3","gene_name":"YTH N6-methyladenosine RNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:26465]","synonyms":"FLJ31657","biotype":"protein_coding","ncbi_id":"253943","summary":"This gene encodes a member of the YTH (YT521-B homology) domain protein family. The YTH domain is common in eukaryotes, is often found in the middle of the protein sequence, and may function in binding to RNA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":63168553,"end":63212786,"strand":1,"description":"YTH N6-methyladenosine RNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:26465]"}, {"versioned_ensembl_gene_id":"ENSG00000112787.12","gene_symbol":"FBRSL1","gene_name":"fibrosin like 1 [Source:HGNC Symbol;Acc:HGNC:29308]","synonyms":"KIAA1545","biotype":"protein_coding","ncbi_id":"57666","summary":null,"start":132489551,"end":132585188,"strand":1,"description":"fibrosin like 1 [Source:HGNC Symbol;Acc:HGNC:29308]"}, {"versioned_ensembl_gene_id":"ENSG00000234534.1","gene_symbol":"CSNK1G2P1","gene_name":"casein kinase 1 gamma 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419821","summary":null,"start":5040945,"end":5041940,"strand":1,"description":"casein kinase 1 gamma 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49739]"}, {"versioned_ensembl_gene_id":"ENSG00000100564.8","gene_symbol":"PIGH","gene_name":"phosphatidylinositol glycan anchor biosynthesis class H [Source:HGNC Symbol;Acc:HGNC:8964]","synonyms":"GPI-H","biotype":"protein_coding","ncbi_id":"5283","summary":"This gene encodes an endoplasmic reticulum associated protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI anchor is a glycolipid found on many blood cells and which serves to anchor proteins to the cell surface. The protein encoded by this gene is a subunit of the GPI N-acetylglucosaminyl (GlcNAc) transferase that transfers GlcNAc to phosphatidylinositol (PI) on the cytoplasmic side of the endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":67581955,"end":67600287,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class H [Source:HGNC Symbol;Acc:HGNC:8964]"}, {"versioned_ensembl_gene_id":"ENSG00000232398.1","gene_symbol":"TMPRSS11CP","gene_name":"transmembrane protease, serine 11C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31934]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100381178","summary":null,"start":67766480,"end":67773854,"strand":-1,"description":"transmembrane protease, serine 11C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31934]"}, {"versioned_ensembl_gene_id":"ENSG00000068354.15","gene_symbol":"TBC1D25","gene_name":"TBC1 domain family member 25 [Source:HGNC Symbol;Acc:HGNC:8092]","synonyms":"OATL1","biotype":"protein_coding","ncbi_id":"4943","summary":"This gene encodes a protein with a TBC domain and functions as a Rab GTPase activating protein. The encoded protein is involved in the fusion of autophagosomes with endosomes and lysosomes. This gene was previously known as ornithine aminotransferase-like 1, but has no similarity to ornithine aminotransferase. [provided by RefSeq, Jan 2017]","start":48539457,"end":48562609,"strand":1,"description":"TBC1 domain family member 25 [Source:HGNC Symbol;Acc:HGNC:8092]"}, {"versioned_ensembl_gene_id":"ENSG00000249965.2","gene_symbol":"CDC42P4","gene_name":"cell division cycle 42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131440","summary":null,"start":109555170,"end":109555732,"strand":1,"description":"cell division cycle 42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44428]"}, {"versioned_ensembl_gene_id":"ENSG00000235788.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529494,"end":29533642,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000163104.17","gene_symbol":"SMARCAD1","gene_name":"SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 [Source:HGNC Symbol;Acc:HGNC:18398]","synonyms":"KIAA1122,ETL1,DKFZP762K2015","biotype":"protein_coding","ncbi_id":"56916","summary":"This gene encodes a member of the SNF subfamily of helicase proteins. The encoded protein plays a critical role in the restoration of heterochromatin organization and propagation of epigenetic patterns following DNA replication by mediating histone H3/H4 deacetylation. Mutations in this gene are associated with adermatoglyphia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":94207611,"end":94291292,"strand":1,"description":"SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 [Source:HGNC Symbol;Acc:HGNC:18398]"}, {"versioned_ensembl_gene_id":"ENSG00000114737.15","gene_symbol":"CISH","gene_name":"cytokine inducible SH2 containing protein [Source:HGNC Symbol;Acc:HGNC:1984]","synonyms":"SOCS,G18,CIS-1,CIS","biotype":"protein_coding","ncbi_id":"1154","summary":"The protein encoded by this gene contains a SH2 domain and a SOCS box domain. The protein thus belongs to the cytokine-induced STAT inhibitor (CIS), also known as suppressor of cytokine signaling (SOCS) or STAT-induced STAT inhibitor (SSI), protein family. CIS family members are known to be cytokine-inducible negative regulators of cytokine signaling. The expression of this gene can be induced by IL2, IL3, GM-CSF and EPO in hematopoietic cells. Proteasome-mediated degradation of this protein has been shown to be involved in the inactivation of the erythropoietin receptor. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":50606490,"end":50611831,"strand":-1,"description":"cytokine inducible SH2 containing protein [Source:HGNC Symbol;Acc:HGNC:1984]"}, {"versioned_ensembl_gene_id":"ENSG00000129353.14","gene_symbol":"SLC44A2","gene_name":"solute carrier family 44 member 2 [Source:HGNC Symbol;Acc:HGNC:17292]","synonyms":"CTL2","biotype":"protein_coding","ncbi_id":"57153","summary":null,"start":10602457,"end":10644559,"strand":1,"description":"solute carrier family 44 member 2 [Source:HGNC Symbol;Acc:HGNC:17292]"}, {"versioned_ensembl_gene_id":"ENSG00000128849.10","gene_symbol":"CGNL1","gene_name":"cingulin like 1 [Source:HGNC Symbol;Acc:HGNC:25931]","synonyms":"PCING,KIAA1749,JACOP,FLJ14957","biotype":"protein_coding","ncbi_id":"84952","summary":"This gene encodes a member of the cingulin family. The encoded protein localizes to both adherens and tight cell-cell junctions and mediates junction assembly and maintenance by regulating the activity of the small GTPases RhoA and Rac1. Heterozygous chromosomal rearrangements resulting in association of the promoter for this gene with the aromatase gene are a cause of aromatase excess syndrome. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Nov 2011]","start":57375967,"end":57550727,"strand":1,"description":"cingulin like 1 [Source:HGNC Symbol;Acc:HGNC:25931]"}, {"versioned_ensembl_gene_id":"ENSG00000254569.1","gene_symbol":"AP002004.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":104873264,"end":104873417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279460.1","gene_symbol":"AC112243.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":184984277,"end":184988127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213568.4","gene_symbol":"HNRNPA1P13","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39131]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131130","summary":null,"start":136428892,"end":136429854,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39131]"}, {"versioned_ensembl_gene_id":"ENSG00000224892.6","gene_symbol":"RPS4XP16","gene_name":"ribosomal protein S4X pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36365]","synonyms":"RPS4P16","biotype":"transcribed_processed_pseudogene","ncbi_id":"220433","summary":null,"start":51454164,"end":51461315,"strand":1,"description":"ribosomal protein S4X pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36365]"}, {"versioned_ensembl_gene_id":"ENSG00000270995.1","gene_symbol":"AL137072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100120435,"end":100120900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215190.9","gene_symbol":"LINC00680","gene_name":"long intergenic non-protein coding RNA 680 [Source:HGNC Symbol;Acc:HGNC:44417]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106660612","summary":null,"start":57946074,"end":57961501,"strand":-1,"description":"long intergenic non-protein coding RNA 680 [Source:HGNC Symbol;Acc:HGNC:44417]"}, {"versioned_ensembl_gene_id":"ENSG00000241186.9","gene_symbol":"TDGF1","gene_name":"teratocarcinoma-derived growth factor 1 [Source:HGNC Symbol;Acc:HGNC:11701]","synonyms":"Cripto-1,CRIPTO,CR","biotype":"protein_coding","ncbi_id":"6997","summary":"This gene encodes an epidermal growth factor-related protein that contains a cripto, FRL-1, and cryptic domain. The encoded protein is an extracellular, membrane-bound signaling protein that plays an essential role in embryonic development and tumor growth. Mutations in this gene are associated with forebrain defects. Pseudogenes of this gene are found on chromosomes 2, 3, 6, 8, 19 and X. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":46574534,"end":46582463,"strand":1,"description":"teratocarcinoma-derived growth factor 1 [Source:HGNC Symbol;Acc:HGNC:11701]"}, {"versioned_ensembl_gene_id":"ENSG00000173338.12","gene_symbol":"KCNK7","gene_name":"potassium two pore domain channel subfamily K member 7 [Source:HGNC Symbol;Acc:HGNC:6282]","synonyms":"K2p7.1","biotype":"protein_coding","ncbi_id":"10089","summary":"This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel; however, it may require other non-pore-forming proteins for activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":65592855,"end":65595996,"strand":-1,"description":"potassium two pore domain channel subfamily K member 7 [Source:HGNC Symbol;Acc:HGNC:6282]"}, {"versioned_ensembl_gene_id":"ENSG00000234235.1","gene_symbol":"BOK-AS1","gene_name":"BOK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:35125]","synonyms":"BOKAS,NCRNA00151,NAToB","biotype":"antisense_RNA","ncbi_id":"100379249","summary":null,"start":241544403,"end":241558977,"strand":-1,"description":"BOK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:35125]"}, {"versioned_ensembl_gene_id":"ENSG00000102878.16","gene_symbol":"HSF4","gene_name":"heat shock transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:5227]","synonyms":"CTM","biotype":"protein_coding","ncbi_id":"3299","summary":"Heat-shock transcription factors (HSFs) activate heat-shock response genes under conditions of heat or other stresses. HSF4 lacks the carboxyl-terminal hydrophobic repeat which is shared among all vertebrate HSFs and has been suggested to be involved in the negative regulation of DNA binding activity. Two alternatively spliced transcripts encoding distinct isoforms and possessing different transcriptional activity have been described. [provided by RefSeq, Jul 2008]","start":67164681,"end":67169945,"strand":1,"description":"heat shock transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:5227]"}, {"versioned_ensembl_gene_id":"ENSG00000185221.6","gene_symbol":"GAPDHP24","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391162","summary":null,"start":214870734,"end":214871716,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37776]"}, {"versioned_ensembl_gene_id":"ENSG00000243004.5","gene_symbol":"AC005062.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":19918981,"end":20140453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078319.9","gene_symbol":"PMS2P1","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9123]","synonyms":"PMSR2,PMSR1,PMS8,PMS3,PMS2L8,PMS2L7,PMS2L6,PMS2L13,PMS2L1","biotype":"unprocessed_pseudogene","ncbi_id":"5379","summary":null,"start":100320992,"end":100341908,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9123]"}, {"versioned_ensembl_gene_id":"ENSG00000224351.2","gene_symbol":"CDKN2AIPNLP3","gene_name":"CDKN2A interacting protein N-terminal like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39853]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874397","summary":null,"start":39817741,"end":39818049,"strand":-1,"description":"CDKN2A interacting protein N-terminal like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39853]"}, {"versioned_ensembl_gene_id":"ENSG00000263171.1","gene_symbol":"AC026954.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7352687,"end":7354944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280382.1","gene_symbol":"AC096920.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50599879,"end":50601148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121742.16","gene_symbol":"GJB6","gene_name":"gap junction protein beta 6 [Source:HGNC Symbol;Acc:HGNC:4288]","synonyms":"ED2,DFNA3,CX30,HED,EDH","biotype":"protein_coding","ncbi_id":"10804","summary":"Gap junctions allow the transport of ions and metabolites between the cytoplasm of adjacent cells. They are formed by two hemichannels, made up of six connexin proteins assembled in groups. Each connexin protein has four transmembrane segments, two extracellular loops, a cytoplasmic loop formed between the two inner transmembrane segments, and the N- and C-terminus both being in the cytoplasm. The specificity of the gap junction is determined by which connexin proteins comprise the hemichannel. In the past, connexin protein names were based on their molecular weight, however the new nomenclature uses sequential numbers based on which form (alpha or beta) of the gap junction is present. This gene encodes one of the connexin proteins. Mutations in this gene have been found in some forms of deafness and in some families with hidrotic ectodermal dysplasia. [provided by RefSeq, Jul 2008]","start":20221971,"end":20232395,"strand":-1,"description":"gap junction protein beta 6 [Source:HGNC Symbol;Acc:HGNC:4288]"}, {"versioned_ensembl_gene_id":"ENSG00000220937.3","gene_symbol":"HNRNPA1P41","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:48770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128701","summary":null,"start":4944670,"end":4945902,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:48770]"}, {"versioned_ensembl_gene_id":"ENSG00000189275.3","gene_symbol":"LINC01164","gene_name":"long intergenic non-protein coding RNA 1164 [Source:HGNC Symbol;Acc:HGNC:49533]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399827","summary":null,"start":131772398,"end":131790199,"strand":-1,"description":"long intergenic non-protein coding RNA 1164 [Source:HGNC Symbol;Acc:HGNC:49533]"}, {"versioned_ensembl_gene_id":"ENSG00000256347.1","gene_symbol":"OR8R1P","gene_name":"olfactory receptor family 8 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15318]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81162","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":73248779,"end":73249867,"strand":1,"description":"olfactory receptor family 8 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15318]"}, {"versioned_ensembl_gene_id":"ENSG00000249975.1","gene_symbol":"OR5H3P","gene_name":"olfactory receptor family 5 subfamily H member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14753]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79309","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98207423,"end":98208341,"strand":1,"description":"olfactory receptor family 5 subfamily H member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14753]"}, {"versioned_ensembl_gene_id":"ENSG00000226902.1","gene_symbol":"CHCHD2P1","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39585]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874506","summary":null,"start":123785009,"end":123785451,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39585]"}, {"versioned_ensembl_gene_id":"ENSG00000217159.2","gene_symbol":"LARP1P1","gene_name":"La ribonucleoprotein domain family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23183]","synonyms":"HCG10P,dJ221C16.7","biotype":"processed_pseudogene","ncbi_id":"100379623","summary":null,"start":26164072,"end":26164363,"strand":1,"description":"La ribonucleoprotein domain family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23183]"}, {"versioned_ensembl_gene_id":"ENSG00000126860.11","gene_symbol":"EVI2A","gene_name":"ecotropic viral integration site 2A [Source:HGNC Symbol;Acc:HGNC:3499]","synonyms":"EVI2,EVDA","biotype":"protein_coding","ncbi_id":"2123","summary":null,"start":31317560,"end":31321884,"strand":-1,"description":"ecotropic viral integration site 2A [Source:HGNC Symbol;Acc:HGNC:3499]"}, {"versioned_ensembl_gene_id":"ENSG00000196866.2","gene_symbol":"HIST1H2AD","gene_name":"histone cluster 1 H2A family member d [Source:HGNC Symbol;Acc:HGNC:4729]","synonyms":"H2AFG,H2A.3,H2A/g","biotype":"protein_coding","ncbi_id":"3013","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26198851,"end":26199243,"strand":-1,"description":"histone cluster 1 H2A family member d [Source:HGNC Symbol;Acc:HGNC:4729]"}, {"versioned_ensembl_gene_id":"ENSG00000100413.16","gene_symbol":"POLR3H","gene_name":"RNA polymerase III subunit H [Source:HGNC Symbol;Acc:HGNC:30349]","synonyms":"RPC8,KIAA1665","biotype":"protein_coding","ncbi_id":"171568","summary":null,"start":41525804,"end":41544606,"strand":-1,"description":"RNA polymerase III subunit H [Source:HGNC Symbol;Acc:HGNC:30349]"}, {"versioned_ensembl_gene_id":"ENSG00000272320.1","gene_symbol":"AL445309.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3311662,"end":3313650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180822.11","gene_symbol":"PSMG4","gene_name":"proteasome assembly chaperone 4 [Source:HGNC Symbol;Acc:HGNC:21108]","synonyms":"PAC4,C6orf86","biotype":"protein_coding","ncbi_id":"389362","summary":null,"start":3231403,"end":3303373,"strand":1,"description":"proteasome assembly chaperone 4 [Source:HGNC Symbol;Acc:HGNC:21108]"}, {"versioned_ensembl_gene_id":"ENSG00000270324.1","gene_symbol":"AC005972.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62978494,"end":62978841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283538.1","gene_symbol":"AC005972.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62910690,"end":62968549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258698.1","gene_symbol":"AL139317.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52792875,"end":52820034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258802.1","gene_symbol":"AL139317.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52798904,"end":52799061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266411.1","gene_symbol":"AC005972.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62966817,"end":62968549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226768.1","gene_symbol":"LINC01149","gene_name":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]","synonyms":"XXbac-BPG181B23.4","biotype":"processed_transcript","ncbi_id":"101929111","summary":null,"start":31435351,"end":31440654,"strand":1,"description":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]"}, {"versioned_ensembl_gene_id":"ENSG00000233186.2","gene_symbol":"KLF4P1","gene_name":"Kruppel like factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49738]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420113","summary":null,"start":4803788,"end":4804972,"strand":-1,"description":"Kruppel like factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49738]"}, {"versioned_ensembl_gene_id":"ENSG00000270270.1","gene_symbol":"BNIP3P10","gene_name":"BCL2 interacting protein 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49690]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421695","summary":null,"start":19870723,"end":19871299,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49690]"}, {"versioned_ensembl_gene_id":"ENSG00000259661.1","gene_symbol":"AC068831.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90920218,"end":90921186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270181.2","gene_symbol":"BIVM-ERCC5","gene_name":"BIVM-ERCC5 readthrough [Source:HGNC Symbol;Acc:HGNC:43690]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533467","summary":"This locus represents naturally occurring read-through transcription between the neighboring BIVM (basic, immunoglobulin-like variable motif containing) and ERCC5 (excision repair cross-complementing rodent repair deficiency, complementation group 5) genes on chromosome 13. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Feb 2011]","start":102799110,"end":102876001,"strand":1,"description":"BIVM-ERCC5 readthrough [Source:HGNC Symbol;Acc:HGNC:43690]"}, {"versioned_ensembl_gene_id":"ENSG00000173838.11","gene_symbol":"MARCH10","gene_name":"membrane associated ring-CH-type finger 10 [Source:HGNC Symbol;Acc:HGNC:26655]","synonyms":"RNF190,MARCH-X,FLJ35757","biotype":"protein_coding","ncbi_id":"162333","summary":"MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010]","start":62701314,"end":62808344,"strand":-1,"description":"membrane associated ring-CH-type finger 10 [Source:HGNC Symbol;Acc:HGNC:26655]"}, {"versioned_ensembl_gene_id":"ENSG00000266947.1","gene_symbol":"AC022916.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35231450,"end":35242963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111816.7","gene_symbol":"FRK","gene_name":"fyn related Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3955]","synonyms":"RAK,PTK5,GTK","biotype":"protein_coding","ncbi_id":"2444","summary":"The protein encoded by this gene belongs to the TYR family of protein kinases. This tyrosine kinase is a nuclear protein and may function during G1 and S phase of the cell cycle and suppress growth. [provided by RefSeq, Jul 2008]","start":115931149,"end":116060758,"strand":-1,"description":"fyn related Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3955]"}, {"versioned_ensembl_gene_id":"ENSG00000240412.1","gene_symbol":"RPL5P15","gene_name":"ribosomal protein L5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36769]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270836","summary":null,"start":58822503,"end":58823714,"strand":1,"description":"ribosomal protein L5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36769]"}, {"versioned_ensembl_gene_id":"ENSG00000164729.7","gene_symbol":"SLC35G3","gene_name":"solute carrier family 35 member G3 [Source:HGNC Symbol;Acc:HGNC:26848]","synonyms":"FLJ40154,AMAC1,TMEM21A","biotype":"protein_coding","ncbi_id":"146861","summary":null,"start":35192520,"end":35194523,"strand":-1,"description":"solute carrier family 35 member G3 [Source:HGNC Symbol;Acc:HGNC:26848]"}, {"versioned_ensembl_gene_id":"ENSG00000174132.8","gene_symbol":"FAM174A","gene_name":"family with sequence similarity 174 member A [Source:HGNC Symbol;Acc:HGNC:24943]","synonyms":"UNQ1912,TMEM157,NS5ATP6","biotype":"protein_coding","ncbi_id":"345757","summary":null,"start":100535305,"end":100586741,"strand":1,"description":"family with sequence similarity 174 member A [Source:HGNC Symbol;Acc:HGNC:24943]"}, {"versioned_ensembl_gene_id":"ENSG00000232112.3","gene_symbol":"TMA7","gene_name":"translation machinery associated 7 homolog [Source:HGNC Symbol;Acc:HGNC:26932]","synonyms":"HSPC016,CCDC72","biotype":"protein_coding","ncbi_id":"51372","summary":null,"start":48440257,"end":48444208,"strand":1,"description":"translation machinery associated 7 homolog [Source:HGNC Symbol;Acc:HGNC:26932]"}, {"versioned_ensembl_gene_id":"ENSG00000255835.1","gene_symbol":"AL117348.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":225886696,"end":225924278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259240.1","gene_symbol":"MIR4713HG","gene_name":"MIR4713 host gene [Source:HGNC Symbol;Acc:HGNC:53124]","synonyms":"RP11-108K3.1","biotype":"lincRNA","ncbi_id":"109729174","summary":null,"start":51037488,"end":51293912,"strand":1,"description":"MIR4713 host gene [Source:HGNC Symbol;Acc:HGNC:53124]"}, {"versioned_ensembl_gene_id":"ENSG00000072415.8","gene_symbol":"MPP5","gene_name":"membrane palmitoylated protein 5 [Source:HGNC Symbol;Acc:HGNC:18669]","synonyms":"FLJ12615,PALS1","biotype":"protein_coding","ncbi_id":"64398","summary":"This gene encodes a member of the p55-like subfamily of the membrane-associated guanylate kinase (MAGUK) gene superfamily. The encoded protein participates in the polarization of differentiating cells, has been shown to regulate myelinating Schwann cells (PMID: 20237282), and is one of the components of the Crumbs complex in the retina. Mice which express lower levels of the orthologous protein have retinal degeneration and impaired vision (PMID: 22114289). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":67241109,"end":67335819,"strand":1,"description":"membrane palmitoylated protein 5 [Source:HGNC Symbol;Acc:HGNC:18669]"}, {"versioned_ensembl_gene_id":"ENSG00000227249.1","gene_symbol":"AC000374.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126511135,"end":126512879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248322.1","gene_symbol":"AL117348.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":225936411,"end":225937557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236340.5","gene_symbol":"AC000099.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127215127,"end":127229921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152932.7","gene_symbol":"RAB3C","gene_name":"RAB3C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30269]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115827","summary":"This gene is a member of the RAS oncogene family and encodes a small GTPase. Other similar small GTPases are known to be involved in vesicle trafficking, and the encoded protein was shown to play a role in recycling phagocytosed MHC class 1 complexes to the cell surface. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":58582221,"end":58859394,"strand":1,"description":"RAB3C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30269]"}, {"versioned_ensembl_gene_id":"ENSG00000247877.6","gene_symbol":"AC021086.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100449754,"end":100535262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270639.1","gene_symbol":"ECM1P1","gene_name":"extracellular matrix protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49736]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420354","summary":null,"start":4768617,"end":4769895,"strand":-1,"description":"extracellular matrix protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49736]"}, {"versioned_ensembl_gene_id":"ENSG00000254952.1","gene_symbol":"AP001257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60159687,"end":60160822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259308.3","gene_symbol":"AC024270.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83044368,"end":83044771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276984.1","gene_symbol":"AL023881.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":424243,"end":424543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139354.10","gene_symbol":"GAS2L3","gene_name":"growth arrest specific 2 like 3 [Source:HGNC Symbol;Acc:HGNC:27475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283431","summary":null,"start":100573683,"end":100628286,"strand":1,"description":"growth arrest specific 2 like 3 [Source:HGNC Symbol;Acc:HGNC:27475]"}, {"versioned_ensembl_gene_id":"ENSG00000228474.5","gene_symbol":"OST4","gene_name":"oligosaccharyltransferase complex subunit 4, non-catalytic [Source:HGNC Symbol;Acc:HGNC:32483]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100128731","summary":null,"start":27070472,"end":27071773,"strand":-1,"description":"oligosaccharyltransferase complex subunit 4, non-catalytic [Source:HGNC Symbol;Acc:HGNC:32483]"}, {"versioned_ensembl_gene_id":"ENSG00000229122.1","gene_symbol":"AGBL5-IT1","gene_name":"AGBL5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41484]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106481744","summary":null,"start":27061038,"end":27061815,"strand":1,"description":"AGBL5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41484]"}, {"versioned_ensembl_gene_id":"ENSG00000042062.11","gene_symbol":"RIPOR3","gene_name":"RIPOR family member 3 [Source:HGNC Symbol;Acc:HGNC:16168]","synonyms":"FAM65C,dJ530I15.3,dJ530I15.2,C20orf176,C20orf175","biotype":"protein_coding","ncbi_id":"140876","summary":null,"start":50586108,"end":50691528,"strand":-1,"description":"RIPOR family member 3 [Source:HGNC Symbol;Acc:HGNC:16168]"}, {"versioned_ensembl_gene_id":"ENSG00000239559.2","gene_symbol":"AP003385.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67682772,"end":67683058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264373.1","gene_symbol":"AC005899.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32434939,"end":32435028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129437.9","gene_symbol":"KLK14","gene_name":"kallikrein related peptidase 14 [Source:HGNC Symbol;Acc:HGNC:6362]","synonyms":"KLK-L6","biotype":"protein_coding","ncbi_id":"43847","summary":"This gene encodes a member of the kallikrein subfamily of serine proteases that have diverse physiological functions such as regulation of blood pressure and desquamation. The altered expression of this gene is implicated in the progression of different cancers including breast and prostate tumors. The encoded protein is a precursor that is proteolytically processed to generate the functional enzyme. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":51077495,"end":51084245,"strand":-1,"description":"kallikrein related peptidase 14 [Source:HGNC Symbol;Acc:HGNC:6362]"}, {"versioned_ensembl_gene_id":"ENSG00000234393.1","gene_symbol":"AL592546.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113710681,"end":113719332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260792.1","gene_symbol":"LINC02280","gene_name":"long intergenic non-protein coding RNA 2280 [Source:HGNC Symbol;Acc:HGNC:53196]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929634","summary":null,"start":104661120,"end":104665558,"strand":-1,"description":"long intergenic non-protein coding RNA 2280 [Source:HGNC Symbol;Acc:HGNC:53196]"}, {"versioned_ensembl_gene_id":"ENSG00000258736.1","gene_symbol":"AL583722.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104653548,"end":104655787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259377.1","gene_symbol":"AC026770.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51752485,"end":51756475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114735.9","gene_symbol":"HEMK1","gene_name":"HemK methyltransferase family member 1 [Source:HGNC Symbol;Acc:HGNC:24923]","synonyms":"MTQ1","biotype":"protein_coding","ncbi_id":"51409","summary":null,"start":50569152,"end":50596168,"strand":1,"description":"HemK methyltransferase family member 1 [Source:HGNC Symbol;Acc:HGNC:24923]"}, {"versioned_ensembl_gene_id":"ENSG00000215808.2","gene_symbol":"LINC01139","gene_name":"long intergenic non-protein coding RNA 1139 [Source:HGNC Symbol;Acc:HGNC:27924]","synonyms":"LINK-A","biotype":"lincRNA","ncbi_id":"339535","summary":null,"start":238480384,"end":238486023,"strand":-1,"description":"long intergenic non-protein coding RNA 1139 [Source:HGNC Symbol;Acc:HGNC:27924]"}, {"versioned_ensembl_gene_id":"ENSG00000230019.1","gene_symbol":"YWHAQP9","gene_name":"YWHAQ pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37688]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101290508","summary":null,"start":238107736,"end":238108567,"strand":-1,"description":"YWHAQ pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37688]"}, {"versioned_ensembl_gene_id":"ENSG00000283294.1","gene_symbol":"AP005212.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":14225224,"end":14342505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230309.1","gene_symbol":"AL121718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78604467,"end":78606036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227547.3","gene_symbol":"OR4A2P","gene_name":"olfactory receptor family 4 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15159]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390133","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54667298,"end":54668210,"strand":1,"description":"olfactory receptor family 4 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15159]"}, {"versioned_ensembl_gene_id":"ENSG00000278134.1","gene_symbol":"AL627230.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67722083,"end":67722683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122691.12","gene_symbol":"TWIST1","gene_name":"twist family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12428]","synonyms":"SCS,H-twist,CRS1,CRS,BPES3,BPES2,bHLHa38,ACS3,TWIST","biotype":"protein_coding","ncbi_id":"7291","summary":"This gene encodes a basic helix-loop-helix (bHLH) transcription factor that plays an important role in embryonic development. The encoded protein forms both homodimers and heterodimers that bind to DNA E box sequences and regulate the transcription of genes involved in cranial suture closure during skull development. This protein may also regulate neural tube closure, limb development and brown fat metabolism. This gene is hypermethylated and overexpressed in multiple human cancers, and the encoded protein promotes tumor cell invasion and metastasis, as well as metastatic recurrence. Mutations in this gene cause Saethre-Chotzen syndrome in human patients, which is characterized by craniosynostosis, ptosis and hypertelorism. [provided by RefSeq, Jul 2020]","start":19020991,"end":19117672,"strand":-1,"description":"twist family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12428]"}, {"versioned_ensembl_gene_id":"ENSG00000105205.6","gene_symbol":"CLC","gene_name":"Charcot-Leyden crystal galectin [Source:HGNC Symbol;Acc:HGNC:2014]","synonyms":"MGC149659,LGALS10,Gal-10","biotype":"protein_coding","ncbi_id":"1178","summary":"Lysophospholipases are enzymes that act on biological membranes to regulate the multifunctional lysophospholipids. The protein encoded by this gene is a lysophospholipase expressed in eosinophils and basophils. It hydrolyzes lysophosphatidylcholine to glycerophosphocholine and a free fatty acid. This protein may possess carbohydrate or IgE-binding activities. It is both structurally and functionally related to the galectin family of beta-galactoside binding proteins. It may be associated with inflammation and some myeloid leukemias. [provided by RefSeq, Jul 2008]","start":39731250,"end":39738028,"strand":-1,"description":"Charcot-Leyden crystal galectin [Source:HGNC Symbol;Acc:HGNC:2014]"}, {"versioned_ensembl_gene_id":"ENSG00000269032.1","gene_symbol":"AC016629.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":58586158,"end":58586356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102870.5","gene_symbol":"ZNF629","gene_name":"zinc finger protein 629 [Source:HGNC Symbol;Acc:HGNC:29008]","synonyms":"ZNF65,KIAA0326","biotype":"protein_coding","ncbi_id":"23361","summary":null,"start":30778449,"end":30787202,"strand":-1,"description":"zinc finger protein 629 [Source:HGNC Symbol;Acc:HGNC:29008]"}, {"versioned_ensembl_gene_id":"ENSG00000269600.1","gene_symbol":"AC016629.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58593896,"end":58599355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267858.5","gene_symbol":"MZF1-AS1","gene_name":"MZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51271]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131691","summary":null,"start":58559129,"end":58574797,"strand":1,"description":"MZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51271]"}, {"versioned_ensembl_gene_id":"ENSG00000235861.1","gene_symbol":"AC005237.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":241118725,"end":241118943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137267.5","gene_symbol":"TUBB2A","gene_name":"tubulin beta 2A class IIa [Source:HGNC Symbol;Acc:HGNC:12412]","synonyms":"TUBB2,TUBB,dJ40E16.7","biotype":"protein_coding","ncbi_id":"7280","summary":"Microtubules, key participants in processes such as mitosis and intracellular transport, are composed of heterodimers of alpha- and beta-tubulins. The protein encoded by this gene is a beta-tubulin. Defects in this gene are associated with complex cortical dysplasia with other brain malformations-5. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":3153669,"end":3157526,"strand":-1,"description":"tubulin beta 2A class IIa [Source:HGNC Symbol;Acc:HGNC:12412]"}, {"versioned_ensembl_gene_id":"ENSG00000266028.7","gene_symbol":"SRGAP2","gene_name":"SLIT-ROBO Rho GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:19751]","synonyms":"SRGAP2A,KIAA0456,FNBP2,ARHGAP34","biotype":"protein_coding","ncbi_id":"23380","summary":"This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. The encoded protein stimulates GTPase activity of Rac1, and plays a role in cortical neuron development. This locus has several paralogs on human chromosome 1 resulting from segmental duplication. While this locus itself is conserved among various species, the paralogs are found only in the genus Homo, and not in the genomes of non-human great apes. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Jul 2014]","start":206203345,"end":206464443,"strand":1,"description":"SLIT-ROBO Rho GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:19751]"}, {"versioned_ensembl_gene_id":"ENSG00000051596.9","gene_symbol":"THOC3","gene_name":"THO complex 3 [Source:HGNC Symbol;Acc:HGNC:19072]","synonyms":"TEX1,MGC5469","biotype":"protein_coding","ncbi_id":"84321","summary":"This gene encodes a component of the nuclear THO transcription elongation complex, which is part of the larger transcription export (TREX) complex that couples messenger RNA processing and export. In humans, the transcription export complex is recruited to the 5'-end of messenger RNAs in a splicing- and cap-dependent manner. Studies of a related complex in mouse suggest that the metazoan transcription export complex is involved in cell differentiation and development. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, May 2013]","start":175917873,"end":176034680,"strand":-1,"description":"THO complex 3 [Source:HGNC Symbol;Acc:HGNC:19072]"}, {"versioned_ensembl_gene_id":"ENSG00000266579.1","gene_symbol":"FO680682.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57493855,"end":57497691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006659.12","gene_symbol":"LGALS14","gene_name":"galectin 14 [Source:HGNC Symbol;Acc:HGNC:30054]","synonyms":"PPL13,CLC2","biotype":"protein_coding","ncbi_id":"56891","summary":"This gene is predominantly expressed in placenta. The encoded protein belongs to the galectin (galaptin/S-lectin) family. The members of galectin family contain one or two carbohydrate recognition domains, which can bind beta-galactoside. Two alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":39704306,"end":39709444,"strand":1,"description":"galectin 14 [Source:HGNC Symbol;Acc:HGNC:30054]"}, {"versioned_ensembl_gene_id":"ENSG00000268153.5","gene_symbol":"AC005176.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39638685,"end":39642401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197462.3","gene_symbol":"AC003975.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125917871,"end":125933832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272572.1","gene_symbol":"AL138762.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100911103,"end":100912739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254537.1","gene_symbol":"AL137161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33403216,"end":33403605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255491.2","gene_symbol":"AC100858.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124811226,"end":124857516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139780.7","gene_symbol":"METTL21C","gene_name":"methyltransferase like 21C [Source:HGNC Symbol;Acc:HGNC:33717]","synonyms":"LOC196541,C13orf39","biotype":"protein_coding","ncbi_id":"196541","summary":null,"start":102685744,"end":102694504,"strand":-1,"description":"methyltransferase like 21C [Source:HGNC Symbol;Acc:HGNC:33717]"}, {"versioned_ensembl_gene_id":"ENSG00000259142.1","gene_symbol":"LINC00644","gene_name":"long intergenic non-protein coding RNA 644 [Source:HGNC Symbol;Acc:HGNC:44297]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101954204","summary":null,"start":62134149,"end":62139973,"strand":-1,"description":"long intergenic non-protein coding RNA 644 [Source:HGNC Symbol;Acc:HGNC:44297]"}, {"versioned_ensembl_gene_id":"ENSG00000273971.1","gene_symbol":"AC009163.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75497948,"end":75498289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102312.21","gene_symbol":"PORCN","gene_name":"porcupine O-acyltransferase [Source:HGNC Symbol;Acc:HGNC:17652]","synonyms":"PPN,PORC,por,MG61,DHOF","biotype":"protein_coding","ncbi_id":"64840","summary":"This gene belongs to the evolutionarily conserved porcupine (Porc) gene family. Genes of the porcupine family encode endoplasmic reticulum proteins with multiple transmembrane domains. Porcupine proteins are involved in the processing of Wnt (wingless and int homologue) proteins. Disruption of this gene is associated with focal dermal hypoplasia, and the encoded protein has been implicated in cancer. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Aug 2013]","start":48508962,"end":48520814,"strand":1,"description":"porcupine O-acyltransferase [Source:HGNC Symbol;Acc:HGNC:17652]"}, {"versioned_ensembl_gene_id":"ENSG00000274691.1","gene_symbol":"AL157834.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95173085,"end":95173187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253180.1","gene_symbol":"AC104986.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99003407,"end":99003842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271283.1","gene_symbol":"AC011458.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19699203,"end":19699409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278402.1","gene_symbol":"AC008984.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54309794,"end":54314056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237548.1","gene_symbol":"TTLL11-IT1","gene_name":"TTLL11 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:24214]","synonyms":"C9orf148","biotype":"lincRNA","ncbi_id":"105376261","summary":null,"start":121884636,"end":121963719,"strand":-1,"description":"TTLL11 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:24214]"}, {"versioned_ensembl_gene_id":"ENSG00000225560.6","gene_symbol":"FAM197Y8","gene_name":"family with sequence similarity 197 Y-linked member 8 [Source:HGNC Symbol;Acc:HGNC:37470]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"105379268","summary":null,"start":9347511,"end":9356814,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 8 [Source:HGNC Symbol;Acc:HGNC:37470]"}, {"versioned_ensembl_gene_id":"ENSG00000178685.13","gene_symbol":"PARP10","gene_name":"poly(ADP-ribose) polymerase family member 10 [Source:HGNC Symbol;Acc:HGNC:25895]","synonyms":"FLJ14464","biotype":"protein_coding","ncbi_id":"84875","summary":"Poly(ADP-ribose) polymerases (PARPs), such as PARP10, regulate gene transcription by altering chromatin organization by adding ADP-ribose to histones. PARPs can also function as transcriptional cofactors (Yu et al., 2005 [PubMed 15674325]).[supplied by OMIM, Mar 2008]","start":143977153,"end":144012772,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 10 [Source:HGNC Symbol;Acc:HGNC:25895]"}, {"versioned_ensembl_gene_id":"ENSG00000277274.1","gene_symbol":"DUX4L22","gene_name":"double homeobox 4 like 22 [Source:HGNC Symbol;Acc:HGNC:50803]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723495","summary":null,"start":133677059,"end":133678327,"strand":1,"description":"double homeobox 4 like 22 [Source:HGNC Symbol;Acc:HGNC:50803]"}, {"versioned_ensembl_gene_id":"ENSG00000274599.2","gene_symbol":"DUX4L24","gene_name":"double homeobox 4 like 24 [Source:HGNC Symbol;Acc:HGNC:50805]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723449","summary":null,"start":133670450,"end":133671718,"strand":1,"description":"double homeobox 4 like 24 [Source:HGNC Symbol;Acc:HGNC:50805]"}, {"versioned_ensembl_gene_id":"ENSG00000280337.1","gene_symbol":"DUX4L25","gene_name":"double homeobox 4 like 25 [Source:HGNC Symbol;Acc:HGNC:50806]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723423","summary":null,"start":133667151,"end":133668419,"strand":1,"description":"double homeobox 4 like 25 [Source:HGNC Symbol;Acc:HGNC:50806]"}, {"versioned_ensembl_gene_id":"ENSG00000205716.4","gene_symbol":"FAM183DP","gene_name":"family with sequence similarity 183 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:51331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060105","summary":null,"start":102249857,"end":102250255,"strand":-1,"description":"family with sequence similarity 183 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:51331]"}, {"versioned_ensembl_gene_id":"ENSG00000223699.8","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"HKE5,DFNB53,DFNA13","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33316561,"end":33346378,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000188993.3","gene_symbol":"LRRC66","gene_name":"leucine rich repeat containing 66 [Source:HGNC Symbol;Acc:HGNC:34299]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339977","summary":"This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. [provided by RefSeq, Apr 2017]","start":51993702,"end":52017620,"strand":-1,"description":"leucine rich repeat containing 66 [Source:HGNC Symbol;Acc:HGNC:34299]"}, {"versioned_ensembl_gene_id":"ENSG00000156504.16","gene_symbol":"FAM122B","gene_name":"family with sequence similarity 122B [Source:HGNC Symbol;Acc:HGNC:30490]","synonyms":"RP11-308B5.5,DKFZp686L20116","biotype":"protein_coding","ncbi_id":"159090","summary":null,"start":134769566,"end":134797232,"strand":-1,"description":"family with sequence similarity 122B [Source:HGNC Symbol;Acc:HGNC:30490]"}, {"versioned_ensembl_gene_id":"ENSG00000280229.1","gene_symbol":"AL161658.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20363691,"end":20365657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276191.4","gene_symbol":"CRHR1","gene_name":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]","synonyms":"CRF1,CRF-R,CRHR,CRF1,CRF-R,CRHR","biotype":"protein_coding","ncbi_id":"1394","summary":"This gene encodes a G-protein coupled receptor that binds neuropeptides of the corticotropin releasing hormone family that are major regulators of the hypothalamic-pituitary-adrenal pathway. The encoded protein is essential for the activation of signal transduction pathways that regulate diverse physiological processes including stress, reproduction, immune response and obesity. Alternative splicing results in multiple transcript variants. Naturally-occurring readthrough transcription between this gene and upstream GeneID:147081 results in transcripts that encode isoforms that share similarity with the products of this gene. [provided by RefSeq, Aug 2016]","start":45795888,"end":45847447,"strand":1,"description":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]"}, {"versioned_ensembl_gene_id":"ENSG00000249465.1","gene_symbol":"RBMXP4","gene_name":"RNA binding motif protein, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:34028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132580","summary":null,"start":109346326,"end":109347459,"strand":-1,"description":"RNA binding motif protein, X-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:34028]"}, {"versioned_ensembl_gene_id":"ENSG00000196187.11","gene_symbol":"TMEM63A","gene_name":"transmembrane protein 63A [Source:HGNC Symbol;Acc:HGNC:29118]","synonyms":"KIAA0792","biotype":"protein_coding","ncbi_id":"9725","summary":null,"start":225845536,"end":225882369,"strand":-1,"description":"transmembrane protein 63A [Source:HGNC Symbol;Acc:HGNC:29118]"}, {"versioned_ensembl_gene_id":"ENSG00000271778.1","gene_symbol":"AC080013.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":158782547,"end":158783124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275951.1","gene_symbol":"AC008984.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54305461,"end":54306170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255733.5","gene_symbol":"IFNG-AS1","gene_name":"IFNG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43910]","synonyms":"Tmevpg1,NEST,LincR-Ifng-3'AS","biotype":"antisense_RNA","ncbi_id":"100885789","summary":null,"start":67989445,"end":68234686,"strand":1,"description":"IFNG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43910]"}, {"versioned_ensembl_gene_id":"ENSG00000100596.6","gene_symbol":"SPTLC2","gene_name":"serine palmitoyltransferase long chain base subunit 2 [Source:HGNC Symbol;Acc:HGNC:11278]","synonyms":"hLCB2a,LCB2A,LCB2,KIAA0526","biotype":"protein_coding","ncbi_id":"9517","summary":"This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011]","start":77505997,"end":77616773,"strand":-1,"description":"serine palmitoyltransferase long chain base subunit 2 [Source:HGNC Symbol;Acc:HGNC:11278]"}, {"versioned_ensembl_gene_id":"ENSG00000257921.5","gene_symbol":"AC025165.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57773028,"end":57787046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256835.1","gene_symbol":"AC005294.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67978107,"end":67978387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233685.1","gene_symbol":"OR6L1P","gene_name":"olfactory receptor family 6 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15124]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390012","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":133575122,"end":133576031,"strand":-1,"description":"olfactory receptor family 6 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15124]"}, {"versioned_ensembl_gene_id":"ENSG00000147650.11","gene_symbol":"LRP12","gene_name":"LDL receptor related protein 12 [Source:HGNC Symbol;Acc:HGNC:31708]","synonyms":"ST7,FLJ12929","biotype":"protein_coding","ncbi_id":"29967","summary":"This gene encodes a member of the low-density lipoprotein receptor related protein family. The product of this gene is a transmembrane protein that is differentially expressed in many cancer cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":104489231,"end":104589024,"strand":-1,"description":"LDL receptor related protein 12 [Source:HGNC Symbol;Acc:HGNC:31708]"}, {"versioned_ensembl_gene_id":"ENSG00000176125.4","gene_symbol":"UFSP1","gene_name":"UFM1 specific peptidase 1 (inactive) [Source:HGNC Symbol;Acc:HGNC:33821]","synonyms":"UFSP","biotype":"protein_coding","ncbi_id":"402682","summary":"This gene encodes a protein that is similar to other Ufm1-specific proteases. Studies in mouse determined that Ufsp1 releases Ufm1 (ubiquitin-fold modifier 1) from its bound conjugated complexes which also makes it into an active form. Because the human UFSP1 protein is shorter on the N-terminus and lacks a conserved Cys active site, it is predicted to be non-functional.[provided by RefSeq, Nov 2009]","start":100888723,"end":100889718,"strand":-1,"description":"UFM1 specific peptidase 1 (inactive) [Source:HGNC Symbol;Acc:HGNC:33821]"}, {"versioned_ensembl_gene_id":"ENSG00000212628.1","gene_symbol":"RNA5SP241","gene_name":"RNA, 5S ribosomal pseudogene 241 [Source:HGNC Symbol;Acc:HGNC:43141]","synonyms":"RN5S241","biotype":"rRNA","ncbi_id":"100873499","summary":null,"start":121083700,"end":121083813,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 241 [Source:HGNC Symbol;Acc:HGNC:43141]"}, {"versioned_ensembl_gene_id":"ENSG00000137106.17","gene_symbol":"GRHPR","gene_name":"glyoxylate and hydroxypyruvate reductase [Source:HGNC Symbol;Acc:HGNC:4570]","synonyms":"PH2,GLXR","biotype":"protein_coding","ncbi_id":"9380","summary":"This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq, Jul 2008]","start":37422666,"end":37436990,"strand":1,"description":"glyoxylate and hydroxypyruvate reductase [Source:HGNC Symbol;Acc:HGNC:4570]"}, {"versioned_ensembl_gene_id":"ENSG00000091136.13","gene_symbol":"LAMB1","gene_name":"laminin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6486]","synonyms":"CLM","biotype":"protein_coding","ncbi_id":"3912","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the beta chain isoform laminin, beta 1. The beta 1 chain has 7 structurally distinct domains which it shares with other beta chain isomers. The C-terminal helical region containing domains I and II are separated by domain alpha, domains III and V contain several EGF-like repeats, and domains IV and VI have a globular conformation. Laminin, beta 1 is expressed in most tissues that produce basement membranes, and is one of the 3 chains constituting laminin 1, the first laminin isolated from Engelbreth-Holm-Swarm (EHS) tumor. A sequence in the beta 1 chain that is involved in cell attachment, chemotaxis, and binding to the laminin receptor was identified and shown to have the capacity to inhibit metastasis. [provided by RefSeq, Aug 2011]","start":107923799,"end":108003255,"strand":-1,"description":"laminin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6486]"}, {"versioned_ensembl_gene_id":"ENSG00000275515.1","gene_symbol":"AC012676.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4433202,"end":4433387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264434.2","gene_symbol":"AC110603.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25302126,"end":25302960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279439.1","gene_symbol":"AC105114.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25200976,"end":25202837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203896.9","gene_symbol":"LIME1","gene_name":"Lck interacting transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:26016]","synonyms":"LIME,FLJ20406,dJ583P15.4","biotype":"protein_coding","ncbi_id":"54923","summary":"This gene encodes a transmembrane adaptor protein that links the T and B-cell receptor stimulation to downstream signaling pathways via its association with the Src family kinases Lck and Lyn, respectively. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":63736283,"end":63739103,"strand":1,"description":"Lck interacting transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:26016]"}, {"versioned_ensembl_gene_id":"ENSG00000232654.1","gene_symbol":"FAM136BP","gene_name":"family with sequence similarity 136 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:21110]","synonyms":"FAM136B,dJ40E16.3,C6orf87","biotype":"processed_pseudogene","ncbi_id":"387071","summary":null,"start":3045384,"end":3045800,"strand":1,"description":"family with sequence similarity 136 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:21110]"}, {"versioned_ensembl_gene_id":"ENSG00000181997.8","gene_symbol":"AQP7P2","gene_name":"aquaporin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32049]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"389756","summary":null,"start":64621560,"end":64637586,"strand":-1,"description":"aquaporin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32049]"}, {"versioned_ensembl_gene_id":"ENSG00000172216.5","gene_symbol":"CEBPB","gene_name":"CCAAT/enhancer binding protein beta [Source:HGNC Symbol;Acc:HGNC:1834]","synonyms":"TCF5,NFIL6,LAP,IL6DBP,CRP2,C/EBP-beta","biotype":"protein_coding","ncbi_id":"1051","summary":"This intronless gene encodes a transcription factor that contains a basic leucine zipper (bZIP) domain. The encoded protein functions as a homodimer but can also form heterodimers with CCAAT/enhancer-binding proteins alpha, delta, and gamma. Activity of this protein is important in the regulation of genes involved in immune and inflammatory responses, among other processes. The use of alternative in-frame AUG start codons results in multiple protein isoforms, each with distinct biological functions. [provided by RefSeq, Oct 2013]","start":50190734,"end":50192689,"strand":1,"description":"CCAAT/enhancer binding protein beta [Source:HGNC Symbol;Acc:HGNC:1834]"}, {"versioned_ensembl_gene_id":"ENSG00000260966.1","gene_symbol":"AP001486.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":103050687,"end":103055799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256211.1","gene_symbol":"AC023512.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16989126,"end":16989936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236697.7","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"NG1,C6orf9,G18.1a,G18.2,AGS4,G18,G18.1b","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32230151,"end":32234908,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000231742.5","gene_symbol":"LINC01273","gene_name":"long intergenic non-protein coding RNA 1273 [Source:HGNC Symbol;Acc:HGNC:50329]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927541","summary":null,"start":50172550,"end":50176671,"strand":1,"description":"long intergenic non-protein coding RNA 1273 [Source:HGNC Symbol;Acc:HGNC:50329]"}, {"versioned_ensembl_gene_id":"ENSG00000162702.7","gene_symbol":"ZNF281","gene_name":"zinc finger protein 281 [Source:HGNC Symbol;Acc:HGNC:13075]","synonyms":"ZBP-99","biotype":"protein_coding","ncbi_id":"23528","summary":null,"start":200404940,"end":200410056,"strand":-1,"description":"zinc finger protein 281 [Source:HGNC Symbol;Acc:HGNC:13075]"}, {"versioned_ensembl_gene_id":"ENSG00000233380.1","gene_symbol":"AC034268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53756989,"end":53757870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242902.1","gene_symbol":"FLNC-AS1","gene_name":"FLNC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53474]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128850162,"end":128862626,"strand":-1,"description":"FLNC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53474]"}, {"versioned_ensembl_gene_id":"ENSG00000242525.1","gene_symbol":"OR7E100P","gene_name":"olfactory receptor family 7 subfamily E member 100 pseudogene [Source:HGNC Symbol;Acc:HGNC:15048]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81430","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":112524187,"end":112525201,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 100 pseudogene [Source:HGNC Symbol;Acc:HGNC:15048]"}, {"versioned_ensembl_gene_id":"ENSG00000103202.12","gene_symbol":"NME4","gene_name":"NME/NM23 nucleoside diphosphate kinase 4 [Source:HGNC Symbol;Acc:HGNC:7852]","synonyms":"NM23H4,nm23-H4,NDPKD","biotype":"protein_coding","ncbi_id":"4833","summary":"The nucleoside diphosphate (NDP) kinases (EC 2.7.4.6) are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates. The enzymes are products of the nm23 gene family, which includes NME4 (Milon et al., 1997 [PubMed 9099850]).[supplied by OMIM, May 2008]","start":396725,"end":410367,"strand":1,"description":"NME/NM23 nucleoside diphosphate kinase 4 [Source:HGNC Symbol;Acc:HGNC:7852]"}, {"versioned_ensembl_gene_id":"ENSG00000234372.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33285042,"end":33297177,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000254572.2","gene_symbol":"AP002469.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122613444,"end":122614486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201634.1","gene_symbol":"SNORD115-48","gene_name":"small nucleolar RNA, C/D box 115-48 [Source:HGNC Symbol;Acc:HGNC:33343]","synonyms":"HBII-52-48","biotype":"snoRNA","ncbi_id":"100033822","summary":null,"start":25269783,"end":25269858,"strand":1,"description":"small nucleolar RNA, C/D box 115-48 [Source:HGNC Symbol;Acc:HGNC:33343]"}, {"versioned_ensembl_gene_id":"ENSG00000200761.1","gene_symbol":"RN7SKP113","gene_name":"RNA, 7SK small nuclear pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:45837]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480465","summary":null,"start":4920770,"end":4921064,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 113 [Source:HGNC Symbol;Acc:HGNC:45837]"}, {"versioned_ensembl_gene_id":"ENSG00000258839.3","gene_symbol":"MC1R","gene_name":"melanocortin 1 receptor [Source:HGNC Symbol;Acc:HGNC:6929]","synonyms":"MSH-R","biotype":"protein_coding","ncbi_id":"4157","summary":"This intronless gene encodes the receptor protein for melanocyte-stimulating hormone (MSH). The encoded protein, a seven pass transmembrane G protein coupled receptor, controls melanogenesis. Two types of melanin exist: red pheomelanin and black eumelanin. Gene mutations that lead to a loss in function are associated with increased pheomelanin production, which leads to lighter skin and hair color. Eumelanin is photoprotective but pheomelanin may contribute to UV-induced skin damage by generating free radicals upon UV radiation. Binding of MSH to its receptor activates the receptor and stimulates eumelanin synthesis. This receptor is a major determining factor in sun sensitivity and is a genetic risk factor for melanoma and non-melanoma skin cancer. Over 30 variant alleles have been identified which correlate with skin and hair color, providing evidence that this gene is an important component in determining normal human pigment variation. [provided by RefSeq, Jul 2008]","start":89912119,"end":89920977,"strand":1,"description":"melanocortin 1 receptor [Source:HGNC Symbol;Acc:HGNC:6929]"}, {"versioned_ensembl_gene_id":"ENSG00000260764.1","gene_symbol":"AC007224.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8731416,"end":8731559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254158.1","gene_symbol":"AC104117.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178997969,"end":178998815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265018.6","gene_symbol":"AGAP12P","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:23661]","synonyms":"CTGLF12P,bA164N7.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"414224","summary":null,"start":48009873,"end":48031640,"strand":-1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:23661]"}, {"versioned_ensembl_gene_id":"ENSG00000168333.13","gene_symbol":"C8orf22","gene_name":"chromosome 8 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:31745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"492307","summary":null,"start":49054311,"end":49076090,"strand":1,"description":"chromosome 8 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:31745]"}, {"versioned_ensembl_gene_id":"ENSG00000157778.8","gene_symbol":"PSMG3","gene_name":"proteasome assembly chaperone 3 [Source:HGNC Symbol;Acc:HGNC:22420]","synonyms":"PAC3,MGC10911,C7orf48","biotype":"protein_coding","ncbi_id":"84262","summary":null,"start":1567330,"end":1571005,"strand":-1,"description":"proteasome assembly chaperone 3 [Source:HGNC Symbol;Acc:HGNC:22420]"}, {"versioned_ensembl_gene_id":"ENSG00000164241.13","gene_symbol":"C5orf63","gene_name":"chromosome 5 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:40051]","synonyms":"YDR286C,FLJ44606","biotype":"protein_coding","ncbi_id":"401207","summary":null,"start":127042558,"end":127073492,"strand":-1,"description":"chromosome 5 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:40051]"}, {"versioned_ensembl_gene_id":"ENSG00000198939.7","gene_symbol":"ZFP2","gene_name":"ZFP2 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:26138]","synonyms":"ZNF751,FLJ21628","biotype":"protein_coding","ncbi_id":"80108","summary":null,"start":178895894,"end":178933212,"strand":1,"description":"ZFP2 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:26138]"}, {"versioned_ensembl_gene_id":"ENSG00000213328.3","gene_symbol":"AC104117.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178909710,"end":178910609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170836.11","gene_symbol":"PPM1D","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1D [Source:HGNC Symbol;Acc:HGNC:9277]","synonyms":"Wip1,PP2C-DELTA","biotype":"protein_coding","ncbi_id":"8493","summary":"The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. The expression of this gene is induced in a p53-dependent manner in response to various environmental stresses. While being induced by tumor suppressor protein TP53/p53, this phosphatase negatively regulates the activity of p38 MAP kinase, MAPK/p38, through which it reduces the phosphorylation of p53, and in turn suppresses p53-mediated transcription and apoptosis. This phosphatase thus mediates a feedback regulation of p38-p53 signaling that contributes to growth inhibition and the suppression of stress induced apoptosis. This gene is located in a chromosomal region known to be amplified in breast cancer. The amplification of this gene has been detected in both breast cancer cell line and primary breast tumors, which suggests a role of this gene in cancer development. [provided by RefSeq, Jul 2008]","start":60600183,"end":60666280,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1D [Source:HGNC Symbol;Acc:HGNC:9277]"}, {"versioned_ensembl_gene_id":"ENSG00000161204.11","gene_symbol":"ABCF3","gene_name":"ATP binding cassette subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:72]","synonyms":"EST201864","biotype":"protein_coding","ncbi_id":"55324","summary":"This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ATP-binding cassette proteins transport various molecules across extra- and intracellular membranes. The protein encoded by this gene displays antiviral effect against flaviviruses. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2017]","start":184186023,"end":184194012,"strand":1,"description":"ATP binding cassette subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:72]"}, {"versioned_ensembl_gene_id":"ENSG00000233161.1","gene_symbol":"DHFRP2","gene_name":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729816","summary":null,"start":31360052,"end":31360598,"strand":-1,"description":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]"}, {"versioned_ensembl_gene_id":"ENSG00000160410.14","gene_symbol":"SHKBP1","gene_name":"SH3KBP1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19214]","synonyms":"Sb1,PP203","biotype":"protein_coding","ncbi_id":"92799","summary":null,"start":40576851,"end":40591399,"strand":1,"description":"SH3KBP1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19214]"}, {"versioned_ensembl_gene_id":"ENSG00000198643.6","gene_symbol":"FAM3D","gene_name":"family with sequence similarity 3 member D [Source:HGNC Symbol;Acc:HGNC:18665]","synonyms":"OIT1,EF7","biotype":"protein_coding","ncbi_id":"131177","summary":null,"start":58633946,"end":58666848,"strand":-1,"description":"family with sequence similarity 3 member D [Source:HGNC Symbol;Acc:HGNC:18665]"}, {"versioned_ensembl_gene_id":"ENSG00000266181.1","gene_symbol":"EIF4A3P1","gene_name":"eukaryotic translation initiation factor 4A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51460]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390843","summary":null,"start":24522273,"end":24522919,"strand":-1,"description":"eukaryotic translation initiation factor 4A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51460]"}, {"versioned_ensembl_gene_id":"ENSG00000198211.8","gene_symbol":"AC092143.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":89919165,"end":89936092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251102.1","gene_symbol":"CTBP2P4","gene_name":"C-terminal binding protein 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45196]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642909","summary":null,"start":98576341,"end":98577260,"strand":1,"description":"C-terminal binding protein 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45196]"}, {"versioned_ensembl_gene_id":"ENSG00000249448.1","gene_symbol":"MTCO1P24","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52089]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075166","summary":null,"start":98410235,"end":98411792,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52089]"}, {"versioned_ensembl_gene_id":"ENSG00000251449.2","gene_symbol":"MTND1P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42094]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873220","summary":null,"start":92702345,"end":92702659,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42094]"}, {"versioned_ensembl_gene_id":"ENSG00000118096.7","gene_symbol":"IFT46","gene_name":"intraflagellar transport 46 [Source:HGNC Symbol;Acc:HGNC:26146]","synonyms":"FLJ21827,CFAP32,C11orf60,C11orf2","biotype":"protein_coding","ncbi_id":"56912","summary":null,"start":118544528,"end":118572970,"strand":-1,"description":"intraflagellar transport 46 [Source:HGNC Symbol;Acc:HGNC:26146]"}, {"versioned_ensembl_gene_id":"ENSG00000274050.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":54957703,"end":54982262,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000206899.1","gene_symbol":"RNU6-36P","gene_name":"RNA, U6 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:34280]","synonyms":"RNU6-36","biotype":"snRNA","ncbi_id":"100873757","summary":null,"start":97721716,"end":97721822,"strand":1,"description":"RNA, U6 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:34280]"}, {"versioned_ensembl_gene_id":"ENSG00000284411.1","gene_symbol":"MIR3191","gene_name":"microRNA 3191 [Source:HGNC Symbol;Acc:HGNC:38222]","synonyms":"hsa-mir-3191","biotype":"miRNA","ncbi_id":"100422832","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47226944,"end":47227019,"strand":-1,"description":"microRNA 3191 [Source:HGNC Symbol;Acc:HGNC:38222]"}, {"versioned_ensembl_gene_id":"ENSG00000275238.1","gene_symbol":"MIR4734","gene_name":"microRNA 4734 [Source:HGNC Symbol;Acc:HGNC:41572]","synonyms":"hsa-mir-4734","biotype":"miRNA","ncbi_id":"100616203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38702262,"end":38702331,"strand":-1,"description":"microRNA 4734 [Source:HGNC Symbol;Acc:HGNC:41572]"}, {"versioned_ensembl_gene_id":"ENSG00000277761.1","gene_symbol":"AC136616.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1167457,"end":1257196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266615.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32054322,"end":32054442,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000221038.1","gene_symbol":"RNU6ATAC7P","gene_name":"RNA, U6atac small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:46906]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479546","summary":null,"start":31563768,"end":31563894,"strand":-1,"description":"RNA, U6atac small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:46906]"}, {"versioned_ensembl_gene_id":"ENSG00000251717.1","gene_symbol":"RNA5SP419","gene_name":"RNA, 5S ribosomal pseudogene 419 [Source:HGNC Symbol;Acc:HGNC:43319]","synonyms":"RN5S419","biotype":"rRNA","ncbi_id":"100873670","summary":null,"start":35753796,"end":35753930,"strand":1,"description":"RNA, 5S ribosomal pseudogene 419 [Source:HGNC Symbol;Acc:HGNC:43319]"}, {"versioned_ensembl_gene_id":"ENSG00000222583.1","gene_symbol":"RN7SKP222","gene_name":"RNA, 7SK small nuclear pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:45946]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479193","summary":null,"start":192093122,"end":192093436,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 222 [Source:HGNC Symbol;Acc:HGNC:45946]"}, {"versioned_ensembl_gene_id":"ENSG00000241757.3","gene_symbol":"RN7SL714P","gene_name":"RNA, 7SL, cytoplasmic 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:46730]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480527","summary":null,"start":98351367,"end":98351664,"strand":-1,"description":"RNA, 7SL, cytoplasmic 714, pseudogene [Source:HGNC Symbol;Acc:HGNC:46730]"}, {"versioned_ensembl_gene_id":"ENSG00000200494.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":16670641,"end":16670742,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207065.1","gene_symbol":"RNU5A-2P","gene_name":"RNA, U5A small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42515]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873830","summary":null,"start":81334303,"end":81334418,"strand":1,"description":"RNA, U5A small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42515]"}, {"versioned_ensembl_gene_id":"ENSG00000284427.1","gene_symbol":"MIR4647","gene_name":"microRNA 4647 [Source:HGNC Symbol;Acc:HGNC:41594]","synonyms":"hsa-mir-4647","biotype":"miRNA","ncbi_id":"100616124","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44254206,"end":44254285,"strand":-1,"description":"microRNA 4647 [Source:HGNC Symbol;Acc:HGNC:41594]"}, {"versioned_ensembl_gene_id":"ENSG00000222932.1","gene_symbol":"RNU6-172P","gene_name":"RNA, U6 small nuclear 172, pseudogene [Source:HGNC Symbol;Acc:HGNC:47135]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479642","summary":null,"start":101796410,"end":101796502,"strand":-1,"description":"RNA, U6 small nuclear 172, pseudogene [Source:HGNC Symbol;Acc:HGNC:47135]"}, {"versioned_ensembl_gene_id":"ENSG00000278223.1","gene_symbol":"MIR6783","gene_name":"microRNA 6783 [Source:HGNC Symbol;Acc:HGNC:50159]","synonyms":"hsa-mir-6783","biotype":"miRNA","ncbi_id":"102466734","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44934618,"end":44934681,"strand":-1,"description":"microRNA 6783 [Source:HGNC Symbol;Acc:HGNC:50159]"}, {"versioned_ensembl_gene_id":"ENSG00000207588.1","gene_symbol":"MIR593","gene_name":"microRNA 593 [Source:HGNC Symbol;Acc:HGNC:32849]","synonyms":"MIRN593,hsa-mir-593","biotype":"miRNA","ncbi_id":"693178","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128081861,"end":128081960,"strand":1,"description":"microRNA 593 [Source:HGNC Symbol;Acc:HGNC:32849]"}, {"versioned_ensembl_gene_id":"ENSG00000251990.1","gene_symbol":"RNA5SP180","gene_name":"RNA, 5S ribosomal pseudogene 180 [Source:HGNC Symbol;Acc:HGNC:43080]","synonyms":"RN5S180","biotype":"rRNA","ncbi_id":"100873442","summary":null,"start":17156971,"end":17157071,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 180 [Source:HGNC Symbol;Acc:HGNC:43080]"}, {"versioned_ensembl_gene_id":"ENSG00000284117.1","gene_symbol":"MIR6883","gene_name":"microRNA 6883 [Source:HGNC Symbol;Acc:HGNC:50019]","synonyms":"hsa-mir-6883","biotype":"miRNA","ncbi_id":"102465532","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8144994,"end":8145071,"strand":-1,"description":"microRNA 6883 [Source:HGNC Symbol;Acc:HGNC:50019]"}, {"versioned_ensembl_gene_id":"ENSG00000243872.3","gene_symbol":"RN7SL464P","gene_name":"RNA, 7SL, cytoplasmic 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:46480]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481049","summary":null,"start":220571739,"end":220572035,"strand":-1,"description":"RNA, 7SL, cytoplasmic 464, pseudogene [Source:HGNC Symbol;Acc:HGNC:46480]"}, {"versioned_ensembl_gene_id":"ENSG00000202249.1","gene_symbol":"RNU5E-5P","gene_name":"RNA, U5E small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42520]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873869","summary":null,"start":101466705,"end":101466820,"strand":1,"description":"RNA, U5E small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42520]"}, {"versioned_ensembl_gene_id":"ENSG00000199762.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47489067,"end":47489170,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280554.1","gene_symbol":"snoU18","gene_name":"Small nucleolar RNA U18 [Source:RFAM;Acc:RF01159]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":66502019,"end":66502089,"strand":-1,"description":"Small nucleolar RNA U18 [Source:RFAM;Acc:RF01159]"}, {"versioned_ensembl_gene_id":"ENSG00000241230.3","gene_symbol":"RN7SL801P","gene_name":"RNA, 7SL, cytoplasmic 801, pseudogene [Source:HGNC Symbol;Acc:HGNC:46817]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481139","summary":null,"start":54048007,"end":54048308,"strand":-1,"description":"RNA, 7SL, cytoplasmic 801, pseudogene [Source:HGNC Symbol;Acc:HGNC:46817]"}, {"versioned_ensembl_gene_id":"ENSG00000276926.1","gene_symbol":"MIR6797","gene_name":"microRNA 6797 [Source:HGNC Symbol;Acc:HGNC:50169]","synonyms":"hsa-mir-6797","biotype":"miRNA","ncbi_id":"102465478","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41869627,"end":41869698,"strand":1,"description":"microRNA 6797 [Source:HGNC Symbol;Acc:HGNC:50169]"}, {"versioned_ensembl_gene_id":"ENSG00000199827.1","gene_symbol":"RNU6-1290P","gene_name":"RNA, U6 small nuclear 1290, pseudogene [Source:HGNC Symbol;Acc:HGNC:48253]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480129","summary":null,"start":175029769,"end":175029877,"strand":1,"description":"RNA, U6 small nuclear 1290, pseudogene [Source:HGNC Symbol;Acc:HGNC:48253]"}, {"versioned_ensembl_gene_id":"ENSG00000283822.1","gene_symbol":"MIR639","gene_name":"microRNA 639 [Source:HGNC Symbol;Acc:HGNC:32895]","synonyms":"MIRN639,hsa-mir-639","biotype":"miRNA","ncbi_id":"693224","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14529543,"end":14529640,"strand":1,"description":"microRNA 639 [Source:HGNC Symbol;Acc:HGNC:32895]"}, {"versioned_ensembl_gene_id":"ENSG00000277049.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":41237440,"end":41237557,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222806.1","gene_symbol":"RNA5SP225","gene_name":"RNA, 5S ribosomal pseudogene 225 [Source:HGNC Symbol;Acc:HGNC:43125]","synonyms":"RN5S225","biotype":"rRNA","ncbi_id":"100873484","summary":null,"start":153420438,"end":153420572,"strand":1,"description":"RNA, 5S ribosomal pseudogene 225 [Source:HGNC Symbol;Acc:HGNC:43125]"}, {"versioned_ensembl_gene_id":"ENSG00000252239.2","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":13297705,"end":13297811,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000206981.1","gene_symbol":"RNU6-40P","gene_name":"RNA, U6 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:34248]","synonyms":"RNU6-40","biotype":"snRNA","ncbi_id":"106480703","summary":null,"start":31497577,"end":31497683,"strand":-1,"description":"RNA, U6 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:34248]"}, {"versioned_ensembl_gene_id":"ENSG00000221033.1","gene_symbol":"MIR1272","gene_name":"microRNA 1272 [Source:HGNC Symbol;Acc:HGNC:35339]","synonyms":"MIRN1272,hsa-mir-1272","biotype":"miRNA","ncbi_id":"100302184","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64762387,"end":64762515,"strand":-1,"description":"microRNA 1272 [Source:HGNC Symbol;Acc:HGNC:35339]"}, {"versioned_ensembl_gene_id":"ENSG00000202169.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61906313,"end":61906408,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252574.2","gene_symbol":"RNU5B-6P","gene_name":"RNA, U5B small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:34186]","synonyms":null,"biotype":"snRNA","ncbi_id":"100147754","summary":null,"start":109184934,"end":109185001,"strand":-1,"description":"RNA, U5B small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:34186]"}, {"versioned_ensembl_gene_id":"ENSG00000276062.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":22611719,"end":22611955,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207201.1","gene_symbol":"RNU1-148P","gene_name":"RNA, U1 small nuclear 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:48490]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481635","summary":null,"start":24076997,"end":24077158,"strand":-1,"description":"RNA, U1 small nuclear 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:48490]"}, {"versioned_ensembl_gene_id":"ENSG00000199798.1","gene_symbol":"SNORD114-5","gene_name":"small nucleolar RNA, C/D box 114-5 [Source:HGNC Symbol;Acc:HGNC:32993]","synonyms":"14q(II-5)","biotype":"snoRNA","ncbi_id":"767581","summary":null,"start":100955370,"end":100955439,"strand":1,"description":"small nucleolar RNA, C/D box 114-5 [Source:HGNC Symbol;Acc:HGNC:32993]"}, {"versioned_ensembl_gene_id":"ENSG00000264482.1","gene_symbol":"MIR4705","gene_name":"microRNA 4705 [Source:HGNC Symbol;Acc:HGNC:41567]","synonyms":"hsa-mir-4705","biotype":"miRNA","ncbi_id":"100616239","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102045934,"end":102046004,"strand":-1,"description":"microRNA 4705 [Source:HGNC Symbol;Acc:HGNC:41567]"}, {"versioned_ensembl_gene_id":"ENSG00000278349.1","gene_symbol":"MIR6754","gene_name":"microRNA 6754 [Source:HGNC Symbol;Acc:HGNC:50203]","synonyms":"hsa-mir-6754","biotype":"miRNA","ncbi_id":"102466728","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71473503,"end":71473568,"strand":1,"description":"microRNA 6754 [Source:HGNC Symbol;Acc:HGNC:50203]"}, {"versioned_ensembl_gene_id":"ENSG00000200922.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":71902455,"end":71902550,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199390.1","gene_symbol":"SNORD114-7","gene_name":"small nucleolar RNA, C/D box 114-7 [Source:HGNC Symbol;Acc:HGNC:32995]","synonyms":"14q(II-7)","biotype":"snoRNA","ncbi_id":"767583","summary":null,"start":100963054,"end":100963130,"strand":1,"description":"small nucleolar RNA, C/D box 114-7 [Source:HGNC Symbol;Acc:HGNC:32995]"}, {"versioned_ensembl_gene_id":"ENSG00000252814.1","gene_symbol":"RN7SKP233","gene_name":"RNA, 7SK small nuclear pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:45957]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480475","summary":null,"start":76287630,"end":76287739,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 233 [Source:HGNC Symbol;Acc:HGNC:45957]"}, {"versioned_ensembl_gene_id":"ENSG00000272237.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":227887631,"end":227887744,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000207873.1","gene_symbol":"MIR513A1","gene_name":"microRNA 513a-1 [Source:HGNC Symbol;Acc:HGNC:32141]","synonyms":"MIRN513A1,MIRN513-1,hsa-mir-513a-1,hsa-mir-513-1","biotype":"miRNA","ncbi_id":"574509","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147213463,"end":147213591,"strand":-1,"description":"microRNA 513a-1 [Source:HGNC Symbol;Acc:HGNC:32141]"}, {"versioned_ensembl_gene_id":"ENSG00000207135.1","gene_symbol":"RNU6-452P","gene_name":"RNA, U6 small nuclear 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:47415]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481322","summary":null,"start":27335501,"end":27335607,"strand":-1,"description":"RNA, U6 small nuclear 452, pseudogene [Source:HGNC Symbol;Acc:HGNC:47415]"}, {"versioned_ensembl_gene_id":"ENSG00000200235.1","gene_symbol":"SNORA27","gene_name":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]","synonyms":"ACA27","biotype":"snoRNA","ncbi_id":"619499","summary":null,"start":140579667,"end":140579792,"strand":1,"description":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]"}, {"versioned_ensembl_gene_id":"ENSG00000207217.1","gene_symbol":"SNORA80D","gene_name":"small nucleolar RNA, H/ACA box 80D [Source:HGNC Symbol;Acc:HGNC:50435]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616999","summary":null,"start":6016877,"end":6017011,"strand":1,"description":"small nucleolar RNA, H/ACA box 80D [Source:HGNC Symbol;Acc:HGNC:50435]"}, {"versioned_ensembl_gene_id":"ENSG00000200789.1","gene_symbol":"RNU1-65P","gene_name":"RNA, U1 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48407]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481614","summary":null,"start":84003332,"end":84003479,"strand":1,"description":"RNA, U1 small nuclear 65, pseudogene [Source:HGNC Symbol;Acc:HGNC:48407]"}, {"versioned_ensembl_gene_id":"ENSG00000207726.3","gene_symbol":"MIR455","gene_name":"microRNA 455 [Source:HGNC Symbol;Acc:HGNC:32344]","synonyms":"MIRN455,hsa-mir-455","biotype":"miRNA","ncbi_id":"619556","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114209434,"end":114209529,"strand":1,"description":"microRNA 455 [Source:HGNC Symbol;Acc:HGNC:32344]"}, {"versioned_ensembl_gene_id":"ENSG00000276680.1","gene_symbol":"HYMAI","gene_name":"Hydatidiform mole associated and imprinted conserved region 1 [Source:RFAM;Acc:RF02143]","synonyms":"NCRNA00020","biotype":"misc_RNA","ncbi_id":"57061","summary":"This gene, which encodes a non-protein coding transcript, exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island, and is expressed only from the paternal allele. It is believed to be one of the causative genes for transient neonatal diabetes mellitus (TNDM), which is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. [provided by RefSeq, Oct 2010]","start":144007227,"end":144007464,"strand":1,"description":"Hydatidiform mole associated and imprinted conserved region 1 [Source:RFAM;Acc:RF02143]"}, {"versioned_ensembl_gene_id":"ENSG00000252650.1","gene_symbol":"RNA5SP75","gene_name":"RNA, 5S ribosomal pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:42852]","synonyms":"RN5S75","biotype":"rRNA","ncbi_id":"100873309","summary":null,"start":204707320,"end":204707430,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:42852]"}, {"versioned_ensembl_gene_id":"ENSG00000222160.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":107650789,"end":107650892,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202024.1","gene_symbol":"RNU6-934P","gene_name":"RNA, U6 small nuclear 934, pseudogene [Source:HGNC Symbol;Acc:HGNC:47897]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481475","summary":null,"start":101325404,"end":101325510,"strand":1,"description":"RNA, U6 small nuclear 934, pseudogene [Source:HGNC Symbol;Acc:HGNC:47897]"}, {"versioned_ensembl_gene_id":"ENSG00000200262.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51107222,"end":51107331,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264926.1","gene_symbol":"MIR378F","gene_name":"microRNA 378f [Source:HGNC Symbol;Acc:HGNC:41686]","synonyms":"hsa-mir-378f","biotype":"miRNA","ncbi_id":"100616492","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23929070,"end":23929147,"strand":1,"description":"microRNA 378f [Source:HGNC Symbol;Acc:HGNC:41686]"}, {"versioned_ensembl_gene_id":"ENSG00000199962.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17576798,"end":17576906,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275215.1","gene_symbol":"RNA5-8SN4","gene_name":"RNA, 5.8S ribosomal N4 [Source:HGNC Symbol;Acc:HGNC:53529]","synonyms":null,"biotype":"rRNA","ncbi_id":"109864274","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. This gene is a representative copy of the 5.8S ribosomal RNA on chromosome 22. [provided by RefSeq, Mar 2017]","start":8395607,"end":8395759,"strand":1,"description":"RNA, 5.8S ribosomal N4 [Source:HGNC Symbol;Acc:HGNC:53529]"}, {"versioned_ensembl_gene_id":"ENSG00000221264.1","gene_symbol":"MIR1284","gene_name":"microRNA 1284 [Source:HGNC Symbol;Acc:HGNC:35362]","synonyms":"MIRN1284,hsa-mir-1284","biotype":"miRNA","ncbi_id":"100302112","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71541970,"end":71542089,"strand":-1,"description":"microRNA 1284 [Source:HGNC Symbol;Acc:HGNC:35362]"}, {"versioned_ensembl_gene_id":"ENSG00000281316.1","gene_symbol":"DPPA2P2","gene_name":"developmental pluripotency associated 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44627]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128503","summary":null,"start":26519354,"end":26520250,"strand":-1,"description":"developmental pluripotency associated 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44627]"}, {"versioned_ensembl_gene_id":"ENSG00000252163.1","gene_symbol":"RN7SKP31","gene_name":"RNA, 7SK small nuclear pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:45755]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480842","summary":null,"start":138397351,"end":138397628,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:45755]"}, {"versioned_ensembl_gene_id":"ENSG00000239703.3","gene_symbol":"RN7SL568P","gene_name":"RNA, 7SL, cytoplasmic 568, pseudogene [Source:HGNC Symbol;Acc:HGNC:46584]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479429","summary":null,"start":56029684,"end":56029981,"strand":-1,"description":"RNA, 7SL, cytoplasmic 568, pseudogene [Source:HGNC Symbol;Acc:HGNC:46584]"}, {"versioned_ensembl_gene_id":"ENSG00000207802.1","gene_symbol":"MIR646","gene_name":"microRNA 646 [Source:HGNC Symbol;Acc:HGNC:32902]","synonyms":"MIRN646,hsa-mir-646","biotype":"miRNA","ncbi_id":"693231","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60308474,"end":60308567,"strand":1,"description":"microRNA 646 [Source:HGNC Symbol;Acc:HGNC:32902]"}, {"versioned_ensembl_gene_id":"ENSG00000274940.1","gene_symbol":"MIR8083","gene_name":"microRNA 8083 [Source:HGNC Symbol;Acc:HGNC:50211]","synonyms":"hsa-mir-8083","biotype":"miRNA","ncbi_id":"102466879","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":153689705,"end":153689793,"strand":-1,"description":"microRNA 8083 [Source:HGNC Symbol;Acc:HGNC:50211]"}, {"versioned_ensembl_gene_id":"ENSG00000263730.1","gene_symbol":"MIR3937","gene_name":"microRNA 3937 [Source:HGNC Symbol;Acc:HGNC:38970]","synonyms":"hsa-mir-3937","biotype":"miRNA","ncbi_id":"100500822","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39661216,"end":39661321,"strand":1,"description":"microRNA 3937 [Source:HGNC Symbol;Acc:HGNC:38970]"}, {"versioned_ensembl_gene_id":"ENSG00000252693.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"ACA40,SNORA40A","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":124197743,"end":124197849,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000207633.3","gene_symbol":"MIR505","gene_name":"microRNA 505 [Source:HGNC Symbol;Acc:HGNC:32140]","synonyms":"MIRN505,hsa-mir-505","biotype":"miRNA","ncbi_id":"574508","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":139924148,"end":139924231,"strand":-1,"description":"microRNA 505 [Source:HGNC Symbol;Acc:HGNC:32140]"}, {"versioned_ensembl_gene_id":"ENSG00000274792.1","gene_symbol":"AC171558.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":386278,"end":387620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277457.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000265981.1","gene_symbol":"MIR544B","gene_name":"microRNA 544b [Source:HGNC Symbol;Acc:HGNC:38361]","synonyms":"hsa-mir-544b","biotype":"miRNA","ncbi_id":"100422864","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124732439,"end":124732516,"strand":1,"description":"microRNA 544b [Source:HGNC Symbol;Acc:HGNC:38361]"}, {"versioned_ensembl_gene_id":"ENSG00000243980.3","gene_symbol":"RN7SL702P","gene_name":"RNA, 7SL, cytoplasmic 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:46718]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481114","summary":null,"start":12273473,"end":12273764,"strand":1,"description":"RNA, 7SL, cytoplasmic 702, pseudogene [Source:HGNC Symbol;Acc:HGNC:46718]"}, {"versioned_ensembl_gene_id":"ENSG00000207019.1","gene_symbol":"RNU6-167P","gene_name":"RNA, U6 small nuclear 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:47130]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481228","summary":null,"start":31345362,"end":31345467,"strand":-1,"description":"RNA, U6 small nuclear 167, pseudogene [Source:HGNC Symbol;Acc:HGNC:47130]"}, {"versioned_ensembl_gene_id":"ENSG00000266006.1","gene_symbol":"MIR4488","gene_name":"microRNA 4488 [Source:HGNC Symbol;Acc:HGNC:41599]","synonyms":"hsa-mir-4488","biotype":"miRNA","ncbi_id":"100616470","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61508596,"end":61508657,"strand":1,"description":"microRNA 4488 [Source:HGNC Symbol;Acc:HGNC:41599]"}, {"versioned_ensembl_gene_id":"ENSG00000275208.1","gene_symbol":"MIR6745","gene_name":"microRNA 6745 [Source:HGNC Symbol;Acc:HGNC:50106]","synonyms":"hsa-mir-6745","biotype":"miRNA","ncbi_id":"102466726","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47179611,"end":47179737,"strand":-1,"description":"microRNA 6745 [Source:HGNC Symbol;Acc:HGNC:50106]"}, {"versioned_ensembl_gene_id":"ENSG00000266407.1","gene_symbol":"MIR3157","gene_name":"microRNA 3157 [Source:HGNC Symbol;Acc:HGNC:38172]","synonyms":"hsa-mir-3157","biotype":"miRNA","ncbi_id":"100422892","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96064315,"end":96064399,"strand":-1,"description":"microRNA 3157 [Source:HGNC Symbol;Acc:HGNC:38172]"}, {"versioned_ensembl_gene_id":"ENSG00000276314.1","gene_symbol":"SNORD107","gene_name":"small nucleolar RNA, C/D box 107 [Source:HGNC Symbol;Acc:HGNC:32771]","synonyms":"HBII-436","biotype":"snoRNA","ncbi_id":"91380","summary":"Small nucleolar RNAs (snoRNAs) are small non-coding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in a cluster of genes including the SNURF-SNRPN gene, which serves as a host for multiple snoRNAs. [provided by RefSeq, Oct 2011]","start":24981994,"end":24982068,"strand":1,"description":"small nucleolar RNA, C/D box 107 [Source:HGNC Symbol;Acc:HGNC:32771]"}, {"versioned_ensembl_gene_id":"ENSG00000200398.1","gene_symbol":"SNORD115-24","gene_name":"small nucleolar RNA, C/D box 115-24 [Source:HGNC Symbol;Acc:HGNC:33043]","synonyms":"HBII-52-24","biotype":"snoRNA","ncbi_id":"100036563","summary":null,"start":25213648,"end":25213729,"strand":1,"description":"small nucleolar RNA, C/D box 115-24 [Source:HGNC Symbol;Acc:HGNC:33043]"}, {"versioned_ensembl_gene_id":"ENSG00000201458.1","gene_symbol":"RNU4-4P","gene_name":"RNA, U4 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10197]","synonyms":"U4/5,U4,RNU4P4","biotype":"snRNA","ncbi_id":"26840","summary":null,"start":172796429,"end":172796558,"strand":-1,"description":"RNA, U4 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10197]"}, {"versioned_ensembl_gene_id":"ENSG00000243954.3","gene_symbol":"RN7SL743P","gene_name":"RNA, 7SL, cytoplasmic 743, pseudogene [Source:HGNC Symbol;Acc:HGNC:46759]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479492","summary":null,"start":8683254,"end":8683551,"strand":1,"description":"RNA, 7SL, cytoplasmic 743, pseudogene [Source:HGNC Symbol;Acc:HGNC:46759]"}, {"versioned_ensembl_gene_id":"ENSG00000265333.1","gene_symbol":"MIR3137","gene_name":"microRNA 3137 [Source:HGNC Symbol;Acc:HGNC:38263]","synonyms":"hsa-mir-3137","biotype":"miRNA","ncbi_id":"100422926","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":195134506,"end":195134580,"strand":-1,"description":"microRNA 3137 [Source:HGNC Symbol;Acc:HGNC:38263]"}, {"versioned_ensembl_gene_id":"ENSG00000273742.1","gene_symbol":"MIR6075","gene_name":"microRNA 6075 [Source:HGNC Symbol;Acc:HGNC:50198]","synonyms":"hsa-mir-6075","biotype":"miRNA","ncbi_id":"102466103","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1510762,"end":1510856,"strand":-1,"description":"microRNA 6075 [Source:HGNC Symbol;Acc:HGNC:50198]"}, {"versioned_ensembl_gene_id":"ENSG00000273948.1","gene_symbol":"SMCR2_1","gene_name":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 1 [Source:RFAM;Acc:RF02177]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17675366,"end":17675522,"strand":1,"description":"Smith-Magenis syndrome chromosome region, candidate 2 conserved region 1 [Source:RFAM;Acc:RF02177]"}, {"versioned_ensembl_gene_id":"ENSG00000266166.2","gene_symbol":"RN7SL557P","gene_name":"RNA, 7SL, cytoplasmic 557, pseudogene [Source:HGNC Symbol;Acc:HGNC:46573]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479425","summary":null,"start":25185253,"end":25185538,"strand":-1,"description":"RNA, 7SL, cytoplasmic 557, pseudogene [Source:HGNC Symbol;Acc:HGNC:46573]"}, {"versioned_ensembl_gene_id":"ENSG00000241064.3","gene_symbol":"RN7SL110P","gene_name":"RNA, 7SL, cytoplasmic 110, pseudogene [Source:HGNC Symbol;Acc:HGNC:46126]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480371","summary":null,"start":15506623,"end":15506905,"strand":-1,"description":"RNA, 7SL, cytoplasmic 110, pseudogene [Source:HGNC Symbol;Acc:HGNC:46126]"}, {"versioned_ensembl_gene_id":"ENSG00000207644.1","gene_symbol":"MIR512-2","gene_name":"microRNA 512-2 [Source:HGNC Symbol;Acc:HGNC:32091]","synonyms":"MIRN512-2,hsa-mir-512-2","biotype":"miRNA","ncbi_id":"574459","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53669157,"end":53669254,"strand":1,"description":"microRNA 512-2 [Source:HGNC Symbol;Acc:HGNC:32091]"}, {"versioned_ensembl_gene_id":"ENSG00000275168.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868924,"end":54869030,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000201098.1","gene_symbol":"RNY1","gene_name":"RNA, Ro-associated Y1 [Source:HGNC Symbol;Acc:HGNC:10242]","synonyms":"hY1","biotype":"misc_RNA","ncbi_id":"6084","summary":"Y RNAs are small noncoding RNAs that were originally identified as the RNA component of soluble ribonucleoproteins (RNPs) termed Ro RNPs. Ro RNPs are detected by autoimmune sera of patients suffering from rheumatic diseases, such as from systemic lupus erythematosus (MIM 152700) and Sjogren syndrome (MIM 270200). Ro RNPs consist of a Y RNA that is associated with the autoimmune antigen proteins Ro60 (TROVE2; MIM 600063) and La (SSB; MIM 109090), as well as other proteins. Four human Y RNAs have been identified: Y1, Y3 (RNY3; MIM 601822), Y4 (RNY4; MIM 601823), and Y5 (RNY5; MIM 601824). (Y2 is a truncated form of Y1.) Y RNAs are transcribed by RNA polymerase III and range in size from 83 to 112 nucleotides. They appear to have a functional role in chromosomal DNA replication (Christov et al., 2006 [PubMed 16943439]).[supplied by OMIM, Apr 2009]","start":148987136,"end":148987248,"strand":-1,"description":"RNA, Ro-associated Y1 [Source:HGNC Symbol;Acc:HGNC:10242]"}, {"versioned_ensembl_gene_id":"ENSG00000199347.1","gene_symbol":"RNU5E-1","gene_name":"RNA, U5E small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10215]","synonyms":"U5E,RNU5E","biotype":"snRNA","ncbi_id":"26829","summary":null,"start":11908152,"end":11908271,"strand":1,"description":"RNA, U5E small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10215]"}, {"versioned_ensembl_gene_id":"ENSG00000274344.1","gene_symbol":"ST7-AS2_1","gene_name":"ST7 antisense RNA 2 conserved region 1 [Source:RFAM;Acc:RF02181]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117117912,"end":117117983,"strand":1,"description":"ST7 antisense RNA 2 conserved region 1 [Source:RFAM;Acc:RF02181]"}, {"versioned_ensembl_gene_id":"ENSG00000201550.1","gene_symbol":"RNU6-726P","gene_name":"RNA, U6 small nuclear 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:47689]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480604","summary":null,"start":131092821,"end":131092927,"strand":-1,"description":"RNA, U6 small nuclear 726, pseudogene [Source:HGNC Symbol;Acc:HGNC:47689]"}, {"versioned_ensembl_gene_id":"ENSG00000251981.1","gene_symbol":"RNU7-52P","gene_name":"RNA, U7 small nuclear 52 pseudogene [Source:HGNC Symbol;Acc:HGNC:34148]","synonyms":"U7.52","biotype":"snRNA","ncbi_id":"100151648","summary":null,"start":62383104,"end":62383166,"strand":1,"description":"RNA, U7 small nuclear 52 pseudogene [Source:HGNC Symbol;Acc:HGNC:34148]"}, {"versioned_ensembl_gene_id":"ENSG00000241868.3","gene_symbol":"RN7SL434P","gene_name":"RNA, 7SL, cytoplasmic 434, pseudogene [Source:HGNC Symbol;Acc:HGNC:46450]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480509","summary":null,"start":196397508,"end":196397778,"strand":-1,"description":"RNA, 7SL, cytoplasmic 434, pseudogene [Source:HGNC Symbol;Acc:HGNC:46450]"}, {"versioned_ensembl_gene_id":"ENSG00000265852.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31486996,"end":31487097,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283556.1","gene_symbol":"MIR376B","gene_name":"microRNA 376b [Source:HGNC Symbol;Acc:HGNC:32066]","synonyms":"MIRN376B,hsa-mir-376b","biotype":"miRNA","ncbi_id":"574435","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101040436,"end":101040535,"strand":1,"description":"microRNA 376b [Source:HGNC Symbol;Acc:HGNC:32066]"}, {"versioned_ensembl_gene_id":"ENSG00000264157.3","gene_symbol":"MIR3127","gene_name":"microRNA 3127 [Source:HGNC Symbol;Acc:HGNC:38269]","synonyms":"hsa-mir-3127","biotype":"miRNA","ncbi_id":"100422928","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96798278,"end":96798353,"strand":1,"description":"microRNA 3127 [Source:HGNC Symbol;Acc:HGNC:38269]"}, {"versioned_ensembl_gene_id":"ENSG00000283848.1","gene_symbol":"MIR6872","gene_name":"microRNA 6872 [Source:HGNC Symbol;Acc:HGNC:50037]","synonyms":"hsa-mir-6872","biotype":"miRNA","ncbi_id":"102465526","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50273236,"end":50273297,"strand":1,"description":"microRNA 6872 [Source:HGNC Symbol;Acc:HGNC:50037]"}, {"versioned_ensembl_gene_id":"ENSG00000252640.1","gene_symbol":"snoU109","gene_name":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":68630851,"end":68630968,"strand":-1,"description":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]"}, {"versioned_ensembl_gene_id":"ENSG00000264229.1","gene_symbol":"RNU4ATAC","gene_name":"RNA, U4atac small nuclear (U12-dependent splicing) [Source:HGNC Symbol;Acc:HGNC:34016]","synonyms":"RNU4ATAC1","biotype":"snRNA","ncbi_id":"100151683","summary":"The small nuclear RNA (snRNA) encoded by this gene is part of the U12-dependent minor spliceosome complex. In addition to the encoded RNA, this ribonucleoprotein complex consists of U11, U12, U5, and U6atac snRNAs. The U12-dependent spliceosome acts on approximately 700 specific introns in the human genome. Defects in this gene are a cause of microcephalic osteodysplastic primordial dwarfism type 1 (MOPD). [provided by RefSeq, Jul 2011]","start":121530881,"end":121531007,"strand":1,"description":"RNA, U4atac small nuclear (U12-dependent splicing) [Source:HGNC Symbol;Acc:HGNC:34016]"}, {"versioned_ensembl_gene_id":"ENSG00000241631.3","gene_symbol":"RN7SL316P","gene_name":"RNA, 7SL, cytoplasmic 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:46332]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479337","summary":null,"start":30702504,"end":30702775,"strand":-1,"description":"RNA, 7SL, cytoplasmic 316, pseudogene [Source:HGNC Symbol;Acc:HGNC:46332]"}, {"versioned_ensembl_gene_id":"ENSG00000274656.1","gene_symbol":"RN7SL625P","gene_name":"RNA, 7SL, cytoplasmic 625, pseudogene [Source:HGNC Symbol;Acc:HGNC:46641]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479450","summary":null,"start":72841437,"end":72841727,"strand":-1,"description":"RNA, 7SL, cytoplasmic 625, pseudogene [Source:HGNC Symbol;Acc:HGNC:46641]"}, {"versioned_ensembl_gene_id":"ENSG00000252776.1","gene_symbol":"RNU4ATAC10P","gene_name":"RNA, U4atac small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:46896]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479542","summary":null,"start":122449210,"end":122449331,"strand":1,"description":"RNA, U4atac small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:46896]"}, {"versioned_ensembl_gene_id":"ENSG00000207113.1","gene_symbol":"RNU6-16P","gene_name":"RNA, U6 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:34260]","synonyms":"RNU6-16","biotype":"snRNA","ncbi_id":"100873753","summary":null,"start":88612805,"end":88612911,"strand":-1,"description":"RNA, U6 small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:34260]"}, {"versioned_ensembl_gene_id":"ENSG00000200796.1","gene_symbol":"RNU6-753P","gene_name":"RNA, U6 small nuclear 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:47716]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479899","summary":null,"start":38396659,"end":38396765,"strand":1,"description":"RNA, U6 small nuclear 753, pseudogene [Source:HGNC Symbol;Acc:HGNC:47716]"}, {"versioned_ensembl_gene_id":"ENSG00000199840.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":184171714,"end":184171823,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252998.1","gene_symbol":"RNU6-889P","gene_name":"RNA, U6 small nuclear 889, pseudogene [Source:HGNC Symbol;Acc:HGNC:47852]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480402","summary":null,"start":2098167,"end":2098269,"strand":1,"description":"RNA, U6 small nuclear 889, pseudogene [Source:HGNC Symbol;Acc:HGNC:47852]"}, {"versioned_ensembl_gene_id":"ENSG00000284146.1","gene_symbol":"MIR922","gene_name":"microRNA 922 [Source:HGNC Symbol;Acc:HGNC:33672]","synonyms":"MIRN922,hsa-mir-922","biotype":"miRNA","ncbi_id":"100126321","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":197674496,"end":197674576,"strand":-1,"description":"microRNA 922 [Source:HGNC Symbol;Acc:HGNC:33672]"}, {"versioned_ensembl_gene_id":"ENSG00000221251.1","gene_symbol":"MIR1263","gene_name":"microRNA 1263 [Source:HGNC Symbol;Acc:HGNC:35329]","synonyms":"MIRN1263,hsa-mir-1263","biotype":"miRNA","ncbi_id":"100302148","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":164171471,"end":164171556,"strand":-1,"description":"microRNA 1263 [Source:HGNC Symbol;Acc:HGNC:35329]"}, {"versioned_ensembl_gene_id":"ENSG00000251939.1","gene_symbol":"RNU6-1278P","gene_name":"RNA, U6 small nuclear 1278, pseudogene [Source:HGNC Symbol;Acc:HGNC:48241]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480124","summary":null,"start":46121615,"end":46121721,"strand":-1,"description":"RNA, U6 small nuclear 1278, pseudogene [Source:HGNC Symbol;Acc:HGNC:48241]"}, {"versioned_ensembl_gene_id":"ENSG00000238966.1","gene_symbol":"SNORD112","gene_name":"Small nucleolar RNA SNORD112 [Source:RFAM;Acc:RF01169]","synonyms":"14q(0)","biotype":"snoRNA","ncbi_id":"692215","summary":"Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":42043504,"end":42043575,"strand":-1,"description":"Small nucleolar RNA SNORD112 [Source:RFAM;Acc:RF01169]"}, {"versioned_ensembl_gene_id":"ENSG00000278447.1","gene_symbol":"MIR6781","gene_name":"microRNA 6781 [Source:HGNC Symbol;Acc:HGNC:50185]","synonyms":"hsa-mir-6781","biotype":"miRNA","ncbi_id":"102465468","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42823880,"end":42823943,"strand":-1,"description":"microRNA 6781 [Source:HGNC Symbol;Acc:HGNC:50185]"}, {"versioned_ensembl_gene_id":"ENSG00000207925.1","gene_symbol":"MIR516B2","gene_name":"microRNA 516b-2 [Source:HGNC Symbol;Acc:HGNC:32117]","synonyms":"MIRN516B2,MIRN516-3,hsa-mir-516b-2,hsa-mir-516-3","biotype":"miRNA","ncbi_id":"574485","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53725442,"end":53725526,"strand":1,"description":"microRNA 516b-2 [Source:HGNC Symbol;Acc:HGNC:32117]"}, {"versioned_ensembl_gene_id":"ENSG00000221052.3","gene_symbol":"MIR1266","gene_name":"microRNA 1266 [Source:HGNC Symbol;Acc:HGNC:35334]","synonyms":"MIRN1266,hsa-mir-1266","biotype":"miRNA","ncbi_id":"100302202","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52277117,"end":52277200,"strand":-1,"description":"microRNA 1266 [Source:HGNC Symbol;Acc:HGNC:35334]"}, {"versioned_ensembl_gene_id":"ENSG00000212156.1","gene_symbol":"RNU6-576P","gene_name":"RNA, U6 small nuclear 576, pseudogene [Source:HGNC Symbol;Acc:HGNC:47539]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479821","summary":null,"start":2199387,"end":2199488,"strand":1,"description":"RNA, U6 small nuclear 576, pseudogene [Source:HGNC Symbol;Acc:HGNC:47539]"}, {"versioned_ensembl_gene_id":"ENSG00000199444.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12088245,"end":12088346,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284135.1","gene_symbol":"MIR3654","gene_name":"microRNA 3654 [Source:HGNC Symbol;Acc:HGNC:38896]","synonyms":"hsa-mir-3654","biotype":"miRNA","ncbi_id":"100500804","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133034860,"end":133034915,"strand":-1,"description":"microRNA 3654 [Source:HGNC Symbol;Acc:HGNC:38896]"}, {"versioned_ensembl_gene_id":"ENSG00000264408.1","gene_symbol":"MIR4470","gene_name":"microRNA 4470 [Source:HGNC Symbol;Acc:HGNC:41833]","synonyms":"hsa-mir-4470","biotype":"miRNA","ncbi_id":"100616484","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61714788,"end":61714859,"strand":1,"description":"microRNA 4470 [Source:HGNC Symbol;Acc:HGNC:41833]"}, {"versioned_ensembl_gene_id":"ENSG00000252649.1","gene_symbol":"RNA5SP480","gene_name":"RNA, 5S ribosomal pseudogene 480 [Source:HGNC Symbol;Acc:HGNC:43380]","synonyms":"RN5S480","biotype":"rRNA","ncbi_id":"100873722","summary":null,"start":31356870,"end":31356978,"strand":1,"description":"RNA, 5S ribosomal pseudogene 480 [Source:HGNC Symbol;Acc:HGNC:43380]"}, {"versioned_ensembl_gene_id":"ENSG00000284032.1","gene_symbol":"MIR29A","gene_name":"microRNA 29a [Source:HGNC Symbol;Acc:HGNC:31616]","synonyms":"MIRN29A,MIRN29,hsa-mir-29a,hsa-mir-29","biotype":"miRNA","ncbi_id":"407021","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130876747,"end":130876810,"strand":-1,"description":"microRNA 29a [Source:HGNC Symbol;Acc:HGNC:31616]"}, {"versioned_ensembl_gene_id":"ENSG00000207316.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88431191,"end":88431309,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283958.1","gene_symbol":"MIR1248","gene_name":"microRNA 1248 [Source:HGNC Symbol;Acc:HGNC:35314]","synonyms":"MIRN1248,hsa-mir-1248","biotype":"miRNA","ncbi_id":"100302143","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":186786672,"end":186786777,"strand":1,"description":"microRNA 1248 [Source:HGNC Symbol;Acc:HGNC:35314]"}, {"versioned_ensembl_gene_id":"ENSG00000275996.1","gene_symbol":"SNORD27","gene_name":"small nucleolar RNA, C/D box 27 [Source:HGNC Symbol;Acc:HGNC:10149]","synonyms":"U27,RNU27","biotype":"snoRNA","ncbi_id":"9301","summary":null,"start":62855012,"end":62855083,"strand":-1,"description":"small nucleolar RNA, C/D box 27 [Source:HGNC Symbol;Acc:HGNC:10149]"}, {"versioned_ensembl_gene_id":"ENSG00000266226.1","gene_symbol":"MIR4323","gene_name":"microRNA 4323 [Source:HGNC Symbol;Acc:HGNC:38394]","synonyms":"hsa-mir-4323","biotype":"miRNA","ncbi_id":"100422980","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42133445,"end":42133513,"strand":-1,"description":"microRNA 4323 [Source:HGNC Symbol;Acc:HGNC:38394]"}, {"versioned_ensembl_gene_id":"ENSG00000277592.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":59584169,"end":59584445,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266570.1","gene_symbol":"MIR5579","gene_name":"microRNA 5579 [Source:HGNC Symbol;Acc:HGNC:43485]","synonyms":"hsa-mir-5579","biotype":"miRNA","ncbi_id":"100847000","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79422169,"end":79422226,"strand":-1,"description":"microRNA 5579 [Source:HGNC Symbol;Acc:HGNC:43485]"}, {"versioned_ensembl_gene_id":"ENSG00000239118.1","gene_symbol":"MIR1972-2","gene_name":"microRNA 1972-2 [Source:HGNC Symbol;Acc:HGNC:38252]","synonyms":"hsa-mir-1972-2","biotype":"miRNA","ncbi_id":"100422922","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70030346,"end":70030422,"strand":1,"description":"microRNA 1972-2 [Source:HGNC Symbol;Acc:HGNC:38252]"}, {"versioned_ensembl_gene_id":"ENSG00000221680.1","gene_symbol":"MIR1278","gene_name":"microRNA 1278 [Source:HGNC Symbol;Acc:HGNC:35356]","synonyms":"hsa-mir-1278,MIRN1278","biotype":"miRNA","ncbi_id":"100302163","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":193136503,"end":193136583,"strand":1,"description":"microRNA 1278 [Source:HGNC Symbol;Acc:HGNC:35356]"}, {"versioned_ensembl_gene_id":"ENSG00000277942.1","gene_symbol":"MIR8075","gene_name":"microRNA 8075 [Source:HGNC Symbol;Acc:HGNC:50172]","synonyms":"hsa-mir-8075","biotype":"miRNA","ncbi_id":"102465874","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113262920,"end":113262999,"strand":1,"description":"microRNA 8075 [Source:HGNC Symbol;Acc:HGNC:50172]"}, {"versioned_ensembl_gene_id":"ENSG00000265814.2","gene_symbol":"RN7SL376P","gene_name":"RNA, 7SL, cytoplasmic 376, pseudogene [Source:HGNC Symbol;Acc:HGNC:46392]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481025","summary":null,"start":40615665,"end":40615928,"strand":-1,"description":"RNA, 7SL, cytoplasmic 376, pseudogene [Source:HGNC Symbol;Acc:HGNC:46392]"}, {"versioned_ensembl_gene_id":"ENSG00000206685.1","gene_symbol":"RNU6-1189P","gene_name":"RNA, U6 small nuclear 1189, pseudogene [Source:HGNC Symbol;Acc:HGNC:48152]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480646","summary":null,"start":47087506,"end":47087612,"strand":1,"description":"RNA, U6 small nuclear 1189, pseudogene [Source:HGNC Symbol;Acc:HGNC:48152]"}, {"versioned_ensembl_gene_id":"ENSG00000264294.1","gene_symbol":"SNORD55","gene_name":"small nucleolar RNA, C/D box 55 [Source:HGNC Symbol;Acc:HGNC:10205]","synonyms":"RNU55,RNU39,U55,U39,SNORD39","biotype":"snoRNA","ncbi_id":"26811","summary":null,"start":44775864,"end":44775943,"strand":1,"description":"small nucleolar RNA, C/D box 55 [Source:HGNC Symbol;Acc:HGNC:10205]"}, {"versioned_ensembl_gene_id":"ENSG00000222145.1","gene_symbol":"SNORA73","gene_name":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":88714242,"end":88714430,"strand":-1,"description":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]"}, {"versioned_ensembl_gene_id":"ENSG00000212230.1","gene_symbol":"RNU6-747P","gene_name":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480399","summary":null,"start":243081156,"end":243081259,"strand":-1,"description":"RNA, U6 small nuclear 747, pseudogene [Source:HGNC Symbol;Acc:HGNC:47710]"}, {"versioned_ensembl_gene_id":"ENSG00000252779.1","gene_symbol":"RNU6-182P","gene_name":"RNA, U6 small nuclear 182, pseudogene [Source:HGNC Symbol;Acc:HGNC:47145]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479647","summary":null,"start":171856566,"end":171856670,"strand":-1,"description":"RNA, U6 small nuclear 182, pseudogene [Source:HGNC Symbol;Acc:HGNC:47145]"}, {"versioned_ensembl_gene_id":"ENSG00000265753.2","gene_symbol":"RN7SL444P","gene_name":"RNA, 7SL, cytoplasmic 444, pseudogene [Source:HGNC Symbol;Acc:HGNC:46460]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479384","summary":null,"start":151300665,"end":151300964,"strand":-1,"description":"RNA, 7SL, cytoplasmic 444, pseudogene [Source:HGNC Symbol;Acc:HGNC:46460]"}, {"versioned_ensembl_gene_id":"ENSG00000251961.1","gene_symbol":"RNU6ATAC13P","gene_name":"RNA, U6atac small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:46912]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479549","summary":null,"start":170891467,"end":170891597,"strand":1,"description":"RNA, U6atac small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:46912]"}, {"versioned_ensembl_gene_id":"ENSG00000207233.1","gene_symbol":"SNORA37","gene_name":"small nucleolar RNA, H/ACA box 37 [Source:HGNC Symbol;Acc:HGNC:32630]","synonyms":"ACA37","biotype":"snoRNA","ncbi_id":"677819","summary":null,"start":54222284,"end":54222412,"strand":-1,"description":"small nucleolar RNA, H/ACA box 37 [Source:HGNC Symbol;Acc:HGNC:32630]"}, {"versioned_ensembl_gene_id":"ENSG00000244425.3","gene_symbol":"RN7SL268P","gene_name":"RNA, 7SL, cytoplasmic 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:46284]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479319","summary":null,"start":23879493,"end":23879790,"strand":-1,"description":"RNA, 7SL, cytoplasmic 268, pseudogene [Source:HGNC Symbol;Acc:HGNC:46284]"}, {"versioned_ensembl_gene_id":"ENSG00000199102.1","gene_symbol":"MIR302C","gene_name":"microRNA 302c [Source:HGNC Symbol;Acc:HGNC:31764]","synonyms":"MIRN302C,hsa-mir-302c","biotype":"miRNA","ncbi_id":"442895","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112648363,"end":112648430,"strand":-1,"description":"microRNA 302c [Source:HGNC Symbol;Acc:HGNC:31764]"}, {"versioned_ensembl_gene_id":"ENSG00000278515.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":36405198,"end":36405304,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000206938.1","gene_symbol":"RNU4-31P","gene_name":"RNA, U4 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:46967]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480546","summary":null,"start":156872078,"end":156872218,"strand":1,"description":"RNA, U4 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:46967]"}, {"versioned_ensembl_gene_id":"ENSG00000207060.1","gene_symbol":"RNU6-480P","gene_name":"RNA, U6 small nuclear 480, pseudogene [Source:HGNC Symbol;Acc:HGNC:47443]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480583","summary":null,"start":51055353,"end":51055459,"strand":-1,"description":"RNA, U6 small nuclear 480, pseudogene [Source:HGNC Symbol;Acc:HGNC:47443]"}, {"versioned_ensembl_gene_id":"ENSG00000275568.4","gene_symbol":"ARHGAP11A","gene_name":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]","synonyms":"KIAA0013,KIAA0013","biotype":"protein_coding","ncbi_id":"9824","summary":"This gene encodes a member of the Rho GTPase activating protein family. In response to DNA damage, the encoded protein interacts with the p53 tumor suppressor protein and stimulates its tetramerization, which results in cell-cycle arrest and apoptosis. A chromosomal deletion that includes this gene is one cause of Prader-Willi syndrome, and an intronic variant of this gene may be associated with sleep duration in children. This gene is highly expressed in colon cancers and in a human basal-like breast cancer cell line. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32695437,"end":32720246,"strand":1,"description":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]"}, {"versioned_ensembl_gene_id":"ENSG00000200891.1","gene_symbol":"SNORD74","gene_name":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]","synonyms":null,"biotype":"snoRNA","ncbi_id":"619498","summary":null,"start":87994618,"end":87994695,"strand":-1,"description":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]"}, {"versioned_ensembl_gene_id":"ENSG00000277401.4","gene_symbol":"TJP1","gene_name":"tight junction protein 1 [Source:HGNC Symbol;Acc:HGNC:11827]","synonyms":"ZO-1,MGC133289,DKFZp686M05161,ZO-1,MGC133289,DKFZp686M05161","biotype":"protein_coding","ncbi_id":"7082","summary":"This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family of proteins, and acts as a tight junction adaptor protein that also regulates adherens junctions. Tight junctions regulate the movement of ions and macromolecules between endothelial and epithelial cells. The multidomain structure of this scaffold protein, including a postsynaptic density 95/disc-large/zona occludens (PDZ) domain, a Src homology (SH3) domain, a guanylate kinase (GuK) domain and unique (U) motifs all help to co-ordinate binding of transmembrane proteins, cytosolic proteins, and F-actin, which are required for tight junction function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]","start":29850002,"end":29972346,"strand":-1,"description":"tight junction protein 1 [Source:HGNC Symbol;Acc:HGNC:11827]"}, {"versioned_ensembl_gene_id":"ENSG00000252118.1","gene_symbol":"RNU6ATAC39P","gene_name":"RNA, U6atac small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:46938]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481172","summary":null,"start":12456483,"end":12456631,"strand":1,"description":"RNA, U6atac small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:46938]"}, {"versioned_ensembl_gene_id":"ENSG00000275939.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":131440031,"end":131440196,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000258002.2","gene_symbol":"CR759815.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31249103,"end":31251125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207496.1","gene_symbol":"SNORA7A","gene_name":"small nucleolar RNA, H/ACA box 7A [Source:HGNC Symbol;Acc:HGNC:32592]","synonyms":"ACA7","biotype":"snoRNA","ncbi_id":"619563","summary":null,"start":12840312,"end":12840450,"strand":-1,"description":"small nucleolar RNA, H/ACA box 7A [Source:HGNC Symbol;Acc:HGNC:32592]"}, {"versioned_ensembl_gene_id":"ENSG00000207170.1","gene_symbol":"RNU6-1215P","gene_name":"RNA, U6 small nuclear 1215, pseudogene [Source:HGNC Symbol;Acc:HGNC:48178]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480097","summary":null,"start":18583367,"end":18583468,"strand":-1,"description":"RNA, U6 small nuclear 1215, pseudogene [Source:HGNC Symbol;Acc:HGNC:48178]"}, {"versioned_ensembl_gene_id":"ENSG00000278348.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74162340,"end":74162620,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265236.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31541101,"end":31541178,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000274847.1","gene_symbol":"AC145212.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53594,"end":115055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278636.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":70430896,"end":70431178,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265535.2","gene_symbol":"RN7SL475P","gene_name":"RNA, 7SL, cytoplasmic 475, pseudogene [Source:HGNC Symbol;Acc:HGNC:46491]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481845","summary":null,"start":59974757,"end":59975054,"strand":-1,"description":"RNA, 7SL, cytoplasmic 475, pseudogene [Source:HGNC Symbol;Acc:HGNC:46491]"}, {"versioned_ensembl_gene_id":"ENSG00000212308.1","gene_symbol":"RNA5SP23","gene_name":"RNA, 5S ribosomal pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42591]","synonyms":"RN5S23","biotype":"rRNA","ncbi_id":"100873278","summary":null,"start":78375164,"end":78375268,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42591]"}, {"versioned_ensembl_gene_id":"ENSG00000202164.1","gene_symbol":"RNA5SP117","gene_name":"RNA, 5S ribosomal pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:42915]","synonyms":"RN5S117","biotype":"rRNA","ncbi_id":"100873387","summary":null,"start":208920547,"end":208920664,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 117 [Source:HGNC Symbol;Acc:HGNC:42915]"}, {"versioned_ensembl_gene_id":"ENSG00000264613.2","gene_symbol":"RN7SL290P","gene_name":"RNA, 7SL, cytoplasmic 290, pseudogene [Source:HGNC Symbol;Acc:HGNC:46306]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481001","summary":null,"start":51995740,"end":51996039,"strand":1,"description":"RNA, 7SL, cytoplasmic 290, pseudogene [Source:HGNC Symbol;Acc:HGNC:46306]"}, {"versioned_ensembl_gene_id":"ENSG00000200472.1","gene_symbol":"RN7SKP44","gene_name":"RNA, 7SK small nuclear pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:45768]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479114","summary":null,"start":31718893,"end":31719208,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:45768]"}, {"versioned_ensembl_gene_id":"ENSG00000206674.1","gene_symbol":"RNU6-945P","gene_name":"RNA, U6 small nuclear 945, pseudogene [Source:HGNC Symbol;Acc:HGNC:47908]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479984","summary":null,"start":40299478,"end":40299584,"strand":-1,"description":"RNA, U6 small nuclear 945, pseudogene [Source:HGNC Symbol;Acc:HGNC:47908]"}, {"versioned_ensembl_gene_id":"ENSG00000239035.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":57278570,"end":57278673,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000252322.1","gene_symbol":"RN7SKP244","gene_name":"RNA, 7SK small nuclear pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:45968]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479203","summary":null,"start":88583666,"end":88583972,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 244 [Source:HGNC Symbol;Acc:HGNC:45968]"}, {"versioned_ensembl_gene_id":"ENSG00000276673.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76733302,"end":76733476,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000201341.1","gene_symbol":"RNU6-421P","gene_name":"RNA, U6 small nuclear 421, pseudogene [Source:HGNC Symbol;Acc:HGNC:47384]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481311","summary":null,"start":49945336,"end":49945442,"strand":-1,"description":"RNA, U6 small nuclear 421, pseudogene [Source:HGNC Symbol;Acc:HGNC:47384]"}, {"versioned_ensembl_gene_id":"ENSG00000281710.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30304321,"end":30304536,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000200269.1","gene_symbol":"RNU6-838P","gene_name":"RNA, U6 small nuclear 838, pseudogene [Source:HGNC Symbol;Acc:HGNC:47801]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479937","summary":null,"start":48106081,"end":48106188,"strand":-1,"description":"RNA, U6 small nuclear 838, pseudogene [Source:HGNC Symbol;Acc:HGNC:47801]"}, {"versioned_ensembl_gene_id":"ENSG00000251727.1","gene_symbol":"RNU6-488P","gene_name":"RNA, U6 small nuclear 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:47451]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479782","summary":null,"start":93843764,"end":93843862,"strand":1,"description":"RNA, U6 small nuclear 488, pseudogene [Source:HGNC Symbol;Acc:HGNC:47451]"}, {"versioned_ensembl_gene_id":"ENSG00000207007.1","gene_symbol":"RNU6-891P","gene_name":"RNA, U6 small nuclear 891, pseudogene [Source:HGNC Symbol;Acc:HGNC:47854]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479960","summary":null,"start":70852130,"end":70852240,"strand":1,"description":"RNA, U6 small nuclear 891, pseudogene [Source:HGNC Symbol;Acc:HGNC:47854]"}, {"versioned_ensembl_gene_id":"ENSG00000263561.1","gene_symbol":"MIR4704","gene_name":"microRNA 4704 [Source:HGNC Symbol;Acc:HGNC:41602]","synonyms":"hsa-mir-4704","biotype":"miRNA","ncbi_id":"100616205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66218250,"end":66218324,"strand":1,"description":"microRNA 4704 [Source:HGNC Symbol;Acc:HGNC:41602]"}, {"versioned_ensembl_gene_id":"ENSG00000264737.1","gene_symbol":"MIR4511","gene_name":"microRNA 4511 [Source:HGNC Symbol;Acc:HGNC:41589]","synonyms":"hsa-mir-4511","biotype":"miRNA","ncbi_id":"100616379","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65719246,"end":65719332,"strand":-1,"description":"microRNA 4511 [Source:HGNC Symbol;Acc:HGNC:41589]"}, {"versioned_ensembl_gene_id":"ENSG00000284488.1","gene_symbol":"MIR6890","gene_name":"microRNA 6890 [Source:HGNC Symbol;Acc:HGNC:49990]","synonyms":"hsa-mir-6890","biotype":"miRNA","ncbi_id":"102465536","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49099854,"end":49099914,"strand":-1,"description":"microRNA 6890 [Source:HGNC Symbol;Acc:HGNC:49990]"}, {"versioned_ensembl_gene_id":"ENSG00000284121.1","gene_symbol":"MIR198","gene_name":"microRNA 198 [Source:HGNC Symbol;Acc:HGNC:31570]","synonyms":"MIRN198,hsa-mir-198","biotype":"miRNA","ncbi_id":"406975","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120395668,"end":120395729,"strand":-1,"description":"microRNA 198 [Source:HGNC Symbol;Acc:HGNC:31570]"}, {"versioned_ensembl_gene_id":"ENSG00000201922.1","gene_symbol":"RNU1-43P","gene_name":"RNA, U1 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:48385]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480159","summary":null,"start":103159960,"end":103160124,"strand":1,"description":"RNA, U1 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:48385]"}, {"versioned_ensembl_gene_id":"ENSG00000222578.1","gene_symbol":"RNA5SP345","gene_name":"RNA, 5S ribosomal pseudogene 345 [Source:HGNC Symbol;Acc:HGNC:43245]","synonyms":"RN5S345","biotype":"rRNA","ncbi_id":"100873607","summary":null,"start":95840017,"end":95840124,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 345 [Source:HGNC Symbol;Acc:HGNC:43245]"}, {"versioned_ensembl_gene_id":"ENSG00000207548.3","gene_symbol":"MIR217","gene_name":"microRNA 217 [Source:HGNC Symbol;Acc:HGNC:31594]","synonyms":"MIRN217,miR-217,hsa-mir-217","biotype":"miRNA","ncbi_id":"406999","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55982967,"end":55983076,"strand":-1,"description":"microRNA 217 [Source:HGNC Symbol;Acc:HGNC:31594]"}, {"versioned_ensembl_gene_id":"ENSG00000265372.1","gene_symbol":"MIR4675","gene_name":"microRNA 4675 [Source:HGNC Symbol;Acc:HGNC:41619]","synonyms":"hsa-mir-4675","biotype":"miRNA","ncbi_id":"100616383","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20551970,"end":20552046,"strand":1,"description":"microRNA 4675 [Source:HGNC Symbol;Acc:HGNC:41619]"}, {"versioned_ensembl_gene_id":"ENSG00000207590.1","gene_symbol":"MIR215","gene_name":"microRNA 215 [Source:HGNC Symbol;Acc:HGNC:31592]","synonyms":"MIRN215,hsa-mir-215","biotype":"miRNA","ncbi_id":"406997","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":220117853,"end":220117962,"strand":-1,"description":"microRNA 215 [Source:HGNC Symbol;Acc:HGNC:31592]"}, {"versioned_ensembl_gene_id":"ENSG00000206842.1","gene_symbol":"RNU6-413P","gene_name":"RNA, U6 small nuclear 413, pseudogene [Source:HGNC Symbol;Acc:HGNC:47376]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479748","summary":null,"start":22787393,"end":22787499,"strand":1,"description":"RNA, U6 small nuclear 413, pseudogene [Source:HGNC Symbol;Acc:HGNC:47376]"}, {"versioned_ensembl_gene_id":"ENSG00000276645.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33029232,"end":33029576,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277604.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":80484589,"end":80484683,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222607.1","gene_symbol":"RNU6-628P","gene_name":"RNA, U6 small nuclear 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:47591]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480396","summary":null,"start":123262843,"end":123262949,"strand":1,"description":"RNA, U6 small nuclear 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:47591]"}, {"versioned_ensembl_gene_id":"ENSG00000280498.1","gene_symbol":"SNORA16A","gene_name":"small nucleolar RNA, H/ACA box 16A [Source:HGNC Symbol;Acc:HGNC:32605]","synonyms":"ACA16,ACA16","biotype":"snoRNA","ncbi_id":"692073","summary":null,"start":28580920,"end":28581054,"strand":-1,"description":"small nucleolar RNA, H/ACA box 16A [Source:HGNC Symbol;Acc:HGNC:32605]"}, {"versioned_ensembl_gene_id":"ENSG00000201114.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":114490724,"end":114490832,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252236.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":156192063,"end":156192203,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000265014.1","gene_symbol":"MIR3160-1","gene_name":"microRNA 3160-1 [Source:HGNC Symbol;Acc:HGNC:38197]","synonyms":"hsa-mir-3160-1","biotype":"miRNA","ncbi_id":"100422827","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46451805,"end":46451889,"strand":-1,"description":"microRNA 3160-1 [Source:HGNC Symbol;Acc:HGNC:38197]"}, {"versioned_ensembl_gene_id":"ENSG00000215943.1","gene_symbol":"MIR892A","gene_name":"microRNA 892a [Source:HGNC Symbol;Acc:HGNC:33639]","synonyms":"MIRN892A,hsa-mir-892a","biotype":"miRNA","ncbi_id":"100126342","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":145996669,"end":145996743,"strand":-1,"description":"microRNA 892a [Source:HGNC Symbol;Acc:HGNC:33639]"}, {"versioned_ensembl_gene_id":"ENSG00000143850.13","gene_symbol":"PLEKHA6","gene_name":"pleckstrin homology domain containing A6 [Source:HGNC Symbol;Acc:HGNC:17053]","synonyms":"PEPP3,KIAA0969","biotype":"protein_coding","ncbi_id":"22874","summary":null,"start":204218851,"end":204377665,"strand":-1,"description":"pleckstrin homology domain containing A6 [Source:HGNC Symbol;Acc:HGNC:17053]"}, {"versioned_ensembl_gene_id":"ENSG00000264698.1","gene_symbol":"MIR4255","gene_name":"microRNA 4255 [Source:HGNC Symbol;Acc:HGNC:38187]","synonyms":"hsa-mir-4255","biotype":"miRNA","ncbi_id":"100422898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37161563,"end":37161634,"strand":1,"description":"microRNA 4255 [Source:HGNC Symbol;Acc:HGNC:38187]"}, {"versioned_ensembl_gene_id":"ENSG00000273946.1","gene_symbol":"RN7SL733P","gene_name":"RNA, 7SL, cytoplasmic 733, pseudogene [Source:HGNC Symbol;Acc:HGNC:46749]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479489","summary":null,"start":87154041,"end":87154369,"strand":-1,"description":"RNA, 7SL, cytoplasmic 733, pseudogene [Source:HGNC Symbol;Acc:HGNC:46749]"}, {"versioned_ensembl_gene_id":"ENSG00000199881.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":92272147,"end":92272250,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207363.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":107901145,"end":107901246,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252014.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":131768140,"end":131768249,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000201368.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":35429064,"end":35429277,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252041.1","gene_symbol":"RNA5SP228","gene_name":"RNA, 5S ribosomal pseudogene 228 [Source:HGNC Symbol;Acc:HGNC:43128]","synonyms":"RN5S228","biotype":"rRNA","ncbi_id":"100873486","summary":null,"start":24132705,"end":24132837,"strand":1,"description":"RNA, 5S ribosomal pseudogene 228 [Source:HGNC Symbol;Acc:HGNC:43128]"}, {"versioned_ensembl_gene_id":"ENSG00000265165.1","gene_symbol":"MIR4307","gene_name":"microRNA 4307 [Source:HGNC Symbol;Acc:HGNC:38257]","synonyms":"hsa-mir-4307","biotype":"miRNA","ncbi_id":"100423019","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26908642,"end":26908725,"strand":1,"description":"microRNA 4307 [Source:HGNC Symbol;Acc:HGNC:38257]"}, {"versioned_ensembl_gene_id":"ENSG00000284114.1","gene_symbol":"MIR6800","gene_name":"microRNA 6800 [Source:HGNC Symbol;Acc:HGNC:50042]","synonyms":"hsa-mir-6800","biotype":"miRNA","ncbi_id":"102465480","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49832018,"end":49832099,"strand":1,"description":"microRNA 6800 [Source:HGNC Symbol;Acc:HGNC:50042]"}, {"versioned_ensembl_gene_id":"ENSG00000202491.1","gene_symbol":"RNU6-716P","gene_name":"RNA, U6 small nuclear 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:47679]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479883","summary":null,"start":200008505,"end":200008607,"strand":-1,"description":"RNA, U6 small nuclear 716, pseudogene [Source:HGNC Symbol;Acc:HGNC:47679]"}, {"versioned_ensembl_gene_id":"ENSG00000273928.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":106661353,"end":106661467,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000222652.1","gene_symbol":"RNU6-248P","gene_name":"RNA, U6 small nuclear 248, pseudogene [Source:HGNC Symbol;Acc:HGNC:47211]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481256","summary":null,"start":76092834,"end":76092940,"strand":1,"description":"RNA, U6 small nuclear 248, pseudogene [Source:HGNC Symbol;Acc:HGNC:47211]"}, {"versioned_ensembl_gene_id":"ENSG00000206912.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23299155,"end":23299262,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241587.3","gene_symbol":"RN7SL482P","gene_name":"RNA, 7SL, cytoplasmic 482, pseudogene [Source:HGNC Symbol;Acc:HGNC:46498]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480513","summary":null,"start":66323855,"end":66324152,"strand":1,"description":"RNA, 7SL, cytoplasmic 482, pseudogene [Source:HGNC Symbol;Acc:HGNC:46498]"}, {"versioned_ensembl_gene_id":"ENSG00000201292.1","gene_symbol":"RNU6-153P","gene_name":"RNA, U6 small nuclear 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:47116]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479634","summary":null,"start":166209403,"end":166209506,"strand":1,"description":"RNA, U6 small nuclear 153, pseudogene [Source:HGNC Symbol;Acc:HGNC:47116]"}, {"versioned_ensembl_gene_id":"ENSG00000200969.1","gene_symbol":"SNORD95","gene_name":"Small nucleolar RNA SNORD95 [Source:RFAM;Acc:RF00189]","synonyms":"U95","biotype":"snoRNA","ncbi_id":"619570","summary":null,"start":81888918,"end":81888985,"strand":1,"description":"Small nucleolar RNA SNORD95 [Source:RFAM;Acc:RF00189]"}, {"versioned_ensembl_gene_id":"ENSG00000273675.1","gene_symbol":"AL118556.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50471769,"end":50472592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145700.9","gene_symbol":"ANKRD31","gene_name":"ankyrin repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:26853]","synonyms":"FLJ40191","biotype":"protein_coding","ncbi_id":"256006","summary":"This gene encodes a protein containing multiple ankyrin repeats. Ankyrin domains function in protein-protein interactions in a variety of cellular processes. Mutations in this gene are associated with a Rett syndrome (RTT)-like phenotype. [provided by RefSeq, Apr 2017]","start":75068275,"end":75236878,"strand":-1,"description":"ankyrin repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:26853]"}, {"versioned_ensembl_gene_id":"ENSG00000182383.8","gene_symbol":"RPL27AP5","gene_name":"ribosomal protein L27a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36420]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271300","summary":null,"start":74990189,"end":74990637,"strand":-1,"description":"ribosomal protein L27a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36420]"}, {"versioned_ensembl_gene_id":"ENSG00000284300.1","gene_symbol":"AC132825.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22531463,"end":22531797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263483.1","gene_symbol":"MTATP6P3","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44577]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479043","summary":null,"start":22529934,"end":22530609,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44577]"}, {"versioned_ensembl_gene_id":"ENSG00000263914.1","gene_symbol":"MTND2P13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42114]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873345","summary":null,"start":22525899,"end":22526937,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42114]"}, {"versioned_ensembl_gene_id":"ENSG00000266885.2","gene_symbol":"AC132825.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":22435390,"end":22439033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282199.1","gene_symbol":"AC007993.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":43914433,"end":43923001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225626.2","gene_symbol":"C9orf135-AS1","gene_name":"C9orf135 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48713]","synonyms":null,"biotype":"lincRNA","ncbi_id":"494558","summary":null,"start":69818983,"end":69820739,"strand":-1,"description":"C9orf135 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48713]"}, {"versioned_ensembl_gene_id":"ENSG00000204711.8","gene_symbol":"C9orf135","gene_name":"chromosome 9 open reading frame 135 [Source:HGNC Symbol;Acc:HGNC:31422]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138255","summary":null,"start":69820793,"end":69906232,"strand":1,"description":"chromosome 9 open reading frame 135 [Source:HGNC Symbol;Acc:HGNC:31422]"}, {"versioned_ensembl_gene_id":"ENSG00000165801.9","gene_symbol":"ARHGEF40","gene_name":"Rho guanine nucleotide exchange factor 40 [Source:HGNC Symbol;Acc:HGNC:25516]","synonyms":"solo,FLJ10357","biotype":"protein_coding","ncbi_id":"55701","summary":"This gene encodes a protein similar to guanosine nucleotide exchange factors for Rho GTPases. The encoded protein contains in its C-terminus a GEF domain involved in exchange activity and a pleckstrin homology domain. Alternatively spliced transcripts that encode different proteins have been described. [provided by RefSeq, Mar 2014]","start":21070270,"end":21090240,"strand":1,"description":"Rho guanine nucleotide exchange factor 40 [Source:HGNC Symbol;Acc:HGNC:25516]"}, {"versioned_ensembl_gene_id":"ENSG00000219433.2","gene_symbol":"BTBD10P2","gene_name":"BTB domain containing 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51541]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420401","summary":null,"start":149794763,"end":149795746,"strand":1,"description":"BTB domain containing 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51541]"}, {"versioned_ensembl_gene_id":"ENSG00000142552.7","gene_symbol":"RCN3","gene_name":"reticulocalbin 3 [Source:HGNC Symbol;Acc:HGNC:21145]","synonyms":"RLP49","biotype":"protein_coding","ncbi_id":"57333","summary":null,"start":49527618,"end":49546962,"strand":1,"description":"reticulocalbin 3 [Source:HGNC Symbol;Acc:HGNC:21145]"}, {"versioned_ensembl_gene_id":"ENSG00000223381.1","gene_symbol":"AL356476.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108710518,"end":108839363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164338.9","gene_symbol":"UTP15","gene_name":"UTP15, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:25758]","synonyms":"FLJ12787,NET21,FLJ23637","biotype":"protein_coding","ncbi_id":"84135","summary":null,"start":73565443,"end":73583377,"strand":1,"description":"UTP15, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:25758]"}, {"versioned_ensembl_gene_id":"ENSG00000073969.18","gene_symbol":"NSF","gene_name":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]","synonyms":"SKD2,SEC18","biotype":"protein_coding","ncbi_id":"4905","summary":null,"start":46590669,"end":46757464,"strand":1,"description":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]"}, {"versioned_ensembl_gene_id":"ENSG00000251031.1","gene_symbol":"AC132803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145222610,"end":145228982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215325.4","gene_symbol":"ASS1P10","gene_name":"argininosuccinate synthetase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:760]","synonyms":"ASSP10","biotype":"processed_pseudogene","ncbi_id":"455","summary":null,"start":145228811,"end":145230054,"strand":1,"description":"argininosuccinate synthetase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:760]"}, {"versioned_ensembl_gene_id":"ENSG00000249229.2","gene_symbol":"NAMPTP2","gene_name":"nicotinamide phosphoribosyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51314]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132712","summary":null,"start":145001853,"end":145005789,"strand":-1,"description":"nicotinamide phosphoribosyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51314]"}, {"versioned_ensembl_gene_id":"ENSG00000213488.4","gene_symbol":"AC008716.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144522140,"end":144522988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137497.17","gene_symbol":"NUMA1","gene_name":"nuclear mitotic apparatus protein 1 [Source:HGNC Symbol;Acc:HGNC:8059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4926","summary":"This gene encodes a large protein that forms a structural component of the nuclear matrix. The encoded protein interacts with microtubules and plays a role in the formation and organization of the mitotic spindle during cell division. Chromosomal translocation of this gene with the RARA (retinoic acid receptor, alpha) gene on chromosome 17 have been detected in patients with acute promyelocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":72002864,"end":72080693,"strand":-1,"description":"nuclear mitotic apparatus protein 1 [Source:HGNC Symbol;Acc:HGNC:8059]"}, {"versioned_ensembl_gene_id":"ENSG00000265099.1","gene_symbol":"AC090774.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20938023,"end":20938344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263986.1","gene_symbol":"AC087393.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20999747,"end":21000323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075413.17","gene_symbol":"MARK3","gene_name":"microtubule affinity regulating kinase 3 [Source:HGNC Symbol;Acc:HGNC:6897]","synonyms":"PAR-1A,KP78,CTAK1","biotype":"protein_coding","ncbi_id":"4140","summary":"The protein encoded by this gene is activated by phosphorylation and in turn is involved in the phosphorylation of tau proteins MAP2 and MAP4. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":103385392,"end":103503831,"strand":1,"description":"microtubule affinity regulating kinase 3 [Source:HGNC Symbol;Acc:HGNC:6897]"}, {"versioned_ensembl_gene_id":"ENSG00000184009.9","gene_symbol":"ACTG1","gene_name":"actin gamma 1 [Source:HGNC Symbol;Acc:HGNC:144]","synonyms":"DFNA20,ACTG,DFNA26","biotype":"protein_coding","ncbi_id":"71","summary":"Actins are highly conserved proteins that are involved in various types of cell motility and in maintenance of the cytoskeleton. Three main groups of actin isoforms have been identified in vertebrate animals: alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":81509971,"end":81523847,"strand":-1,"description":"actin gamma 1 [Source:HGNC Symbol;Acc:HGNC:144]"}, {"versioned_ensembl_gene_id":"ENSG00000278200.1","gene_symbol":"LINC01971","gene_name":"long intergenic non-protein coding RNA 1971 [Source:HGNC Symbol;Acc:HGNC:52797]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371927","summary":null,"start":81480523,"end":81481570,"strand":-1,"description":"long intergenic non-protein coding RNA 1971 [Source:HGNC Symbol;Acc:HGNC:52797]"}, {"versioned_ensembl_gene_id":"ENSG00000279187.1","gene_symbol":"AC027601.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81262920,"end":81265401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279130.1","gene_symbol":"AC091925.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":143406959,"end":143407420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183576.12","gene_symbol":"SETD3","gene_name":"SET domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20493]","synonyms":"FLJ23027,C14orf154","biotype":"protein_coding","ncbi_id":"84193","summary":null,"start":99397746,"end":99480889,"strand":-1,"description":"SET domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20493]"}, {"versioned_ensembl_gene_id":"ENSG00000259155.2","gene_symbol":"AL591767.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49677369,"end":49677893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264874.1","gene_symbol":"AC087499.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20710425,"end":20710533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225768.1","gene_symbol":"AL161646.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104474939,"end":104480274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278899.1","gene_symbol":"AL358852.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149717621,"end":149718888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119392.14","gene_symbol":"GLE1","gene_name":"GLE1, RNA export mediator [Source:HGNC Symbol;Acc:HGNC:4315]","synonyms":"LCCS1,hGLE1,GLE1L","biotype":"protein_coding","ncbi_id":"2733","summary":"This gene encodes a predicted 75-kDa polypeptide with high sequence and structure homology to yeast Gle1p, which is nuclear protein with a leucine-rich nuclear export sequence essential for poly(A)+RNA export. Inhibition of human GLE1L by microinjection of antibodies against GLE1L in HeLa cells resulted in inhibition of poly(A)+RNA export. Immunoflourescence studies show that GLE1L is localized at the nuclear pore complexes. This localization suggests that GLE1L may act at a terminal step in the export of mature RNA messages to the cytoplasm. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":128504700,"end":128542288,"strand":1,"description":"GLE1, RNA export mediator [Source:HGNC Symbol;Acc:HGNC:4315]"}, {"versioned_ensembl_gene_id":"ENSG00000278990.1","gene_symbol":"AL132796.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":98916902,"end":98917801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225163.4","gene_symbol":"LINC00618","gene_name":"long intergenic non-protein coding RNA 618 [Source:HGNC Symbol;Acc:HGNC:20110]","synonyms":"C14orf63","biotype":"sense_overlapping","ncbi_id":"145249","summary":null,"start":96931367,"end":96945394,"strand":1,"description":"long intergenic non-protein coding RNA 618 [Source:HGNC Symbol;Acc:HGNC:20110]"}, {"versioned_ensembl_gene_id":"ENSG00000267496.4","gene_symbol":"FAM215A","gene_name":"family with sequence similarity 215 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17505]","synonyms":"LINC00530,C17orf88,APR-2","biotype":"lincRNA","ncbi_id":"23591","summary":null,"start":43917194,"end":43917985,"strand":1,"description":"family with sequence similarity 215 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17505]"}, {"versioned_ensembl_gene_id":"ENSG00000065621.14","gene_symbol":"GSTO2","gene_name":"glutathione S-transferase omega 2 [Source:HGNC Symbol;Acc:HGNC:23064]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119391","summary":"The protein encoded by this gene is an omega class glutathione S-transferase (GST). GSTs are involved in the metabolism of xenobiotics and carcinogens. Four transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]","start":104268873,"end":104304945,"strand":1,"description":"glutathione S-transferase omega 2 [Source:HGNC Symbol;Acc:HGNC:23064]"}, {"versioned_ensembl_gene_id":"ENSG00000258377.1","gene_symbol":"AL139099.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49620815,"end":49623480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168282.5","gene_symbol":"MGAT2","gene_name":"mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7045]","synonyms":"GNT-II","biotype":"protein_coding","ncbi_id":"4247","summary":"The product of this gene is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans. The enzyme has the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain, and a C-terminal catalytic domain. Mutations in this gene may lead to carbohydrate-deficient glycoprotein syndrome, type II. The coding region of this gene is intronless. Transcript variants with a spliced 5' UTR may exist, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":49620795,"end":49623481,"strand":1,"description":"mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7045]"}, {"versioned_ensembl_gene_id":"ENSG00000108840.15","gene_symbol":"HDAC5","gene_name":"histone deacetylase 5 [Source:HGNC Symbol;Acc:HGNC:14068]","synonyms":"NY-CO-9,KIAA0600,FLJ90614","biotype":"protein_coding","ncbi_id":"10014","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to the class II histone deacetylase/acuc/apha family. It possesses histone deacetylase activity and represses transcription when tethered to a promoter. It coimmunoprecipitates only with HDAC3 family member and might form multicomplex proteins. It also interacts with myocyte enhancer factor-2 (MEF2) proteins, resulting in repression of MEF2-dependent genes. This gene is thought to be associated with colon cancer. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":44076746,"end":44123702,"strand":-1,"description":"histone deacetylase 5 [Source:HGNC Symbol;Acc:HGNC:14068]"}, {"versioned_ensembl_gene_id":"ENSG00000165502.6","gene_symbol":"RPL36AL","gene_name":"ribosomal protein L36a like [Source:HGNC Symbol;Acc:HGNC:10346]","synonyms":"RPL36A","biotype":"protein_coding","ncbi_id":"6166","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which shares sequence similarity with yeast ribosomal protein L44, belongs to the L44E (L36AE) family of ribosomal proteins. This gene and the human gene officially named ribosomal protein L36a (RPL36A) encode nearly identical proteins; however, they are distinct genes. Although the name of this gene has been referred to as ribosomal protein L36a (RPL36A), its official name is ribosomal protein L36a-like (RPL36AL). As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":49618519,"end":49620685,"strand":-1,"description":"ribosomal protein L36a like [Source:HGNC Symbol;Acc:HGNC:10346]"}, {"versioned_ensembl_gene_id":"ENSG00000264981.1","gene_symbol":"AC015818.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20542974,"end":20544123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271588.1","gene_symbol":"LARP7P1","gene_name":"La ribonucleoprotein domain family member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49763]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480287","summary":null,"start":203400266,"end":203400581,"strand":-1,"description":"La ribonucleoprotein domain family member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49763]"}, {"versioned_ensembl_gene_id":"ENSG00000260907.1","gene_symbol":"AC015818.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20530042,"end":20530881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245146.6","gene_symbol":"LINC01024","gene_name":"long intergenic non-protein coding RNA 1024 [Source:HGNC Symbol;Acc:HGNC:49009]","synonyms":"MA-linc1","biotype":"antisense_RNA","ncbi_id":"100505636","summary":null,"start":140072857,"end":140108630,"strand":-1,"description":"long intergenic non-protein coding RNA 1024 [Source:HGNC Symbol;Acc:HGNC:49009]"}, {"versioned_ensembl_gene_id":"ENSG00000259755.1","gene_symbol":"AC090907.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101050732,"end":101086066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259583.2","gene_symbol":"AC015712.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100892859,"end":100919283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280351.2","gene_symbol":"AC127496.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81003335,"end":81005132,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161618.9","gene_symbol":"ALDH16A1","gene_name":"aldehyde dehydrogenase 16 family member A1 [Source:HGNC Symbol;Acc:HGNC:28114]","synonyms":"MGC10204","biotype":"protein_coding","ncbi_id":"126133","summary":"This gene encodes a member of the aldehyde dehydrogenase superfamily. The family members act on aldehyde substrates and use nicotinamide adenine dinucleotide phosphate (NADP) as a cofactor. This gene is conserved in chimpanzee, dog, cow, mouse, rat, and zebrafish. The protein encoded by this gene interacts with maspardin, a protein that when truncated is responsible for Mast syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]","start":49453169,"end":49471048,"strand":1,"description":"aldehyde dehydrogenase 16 family member A1 [Source:HGNC Symbol;Acc:HGNC:28114]"}, {"versioned_ensembl_gene_id":"ENSG00000283029.1","gene_symbol":"AL139099.5","gene_name":null,"synonyms":null,"biotype":"non_coding","ncbi_id":null,"summary":null,"start":49586579,"end":49586878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142541.16","gene_symbol":"RPL13A","gene_name":"ribosomal protein L13a [Source:HGNC Symbol;Acc:HGNC:10304]","synonyms":"TSTA1,L13A","biotype":"protein_coding","ncbi_id":"23521","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L13P family of ribosomal proteins that is a component of the 60S subunit. The encoded protein also plays a role in the repression of inflammatory genes as a component of the IFN-gamma-activated inhibitor of translation (GAIT) complex. This gene is co-transcribed with the small nucleolar RNA genes U32, U33, U34, and U35, which are located in the second, fourth, fifth, and sixth introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":49487554,"end":49492308,"strand":1,"description":"ribosomal protein L13a [Source:HGNC Symbol;Acc:HGNC:10304]"}, {"versioned_ensembl_gene_id":"ENSG00000226272.5","gene_symbol":"ARHGAP26-AS1","gene_name":"ARHGAP26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40792]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874239","summary":null,"start":142859604,"end":142868922,"strand":-1,"description":"ARHGAP26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40792]"}, {"versioned_ensembl_gene_id":"ENSG00000279273.1","gene_symbol":"AC120024.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80463451,"end":80465593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230789.1","gene_symbol":"ARHGAP26-IT1","gene_name":"ARHGAP26 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41429]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874372","summary":null,"start":143192500,"end":143194166,"strand":1,"description":"ARHGAP26 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41429]"}, {"versioned_ensembl_gene_id":"ENSG00000263069.5","gene_symbol":"AC124319.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80351828,"end":80415168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173818.16","gene_symbol":"ENDOV","gene_name":"endonuclease V [Source:HGNC Symbol;Acc:HGNC:26640]","synonyms":"FLJ35220","biotype":"protein_coding","ncbi_id":"284131","summary":null,"start":80415165,"end":80438086,"strand":1,"description":"endonuclease V [Source:HGNC Symbol;Acc:HGNC:26640]"}, {"versioned_ensembl_gene_id":"ENSG00000271792.1","gene_symbol":"AC008667.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139775305,"end":139775472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251387.1","gene_symbol":"AC008667.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139772528,"end":139775406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251568.1","gene_symbol":"ALG3P1","gene_name":"ALG3, alpha-1,3- mannosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45159]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442131","summary":null,"start":5375723,"end":5376836,"strand":-1,"description":"ALG3, alpha-1,3- mannosyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45159]"}, {"versioned_ensembl_gene_id":"ENSG00000148331.11","gene_symbol":"ASB6","gene_name":"ankyrin repeat and SOCS box containing 6 [Source:HGNC Symbol;Acc:HGNC:17181]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140459","summary":"The protein encoded by this gene belongs to a family of ankyrin repeat proteins that, along with four other protein families, contain a C-terminal SOCS box motif. Growing evidence suggests that the SOCS box, similar to the F-box, acts as a bridge between specific substrate-binding domains and the more generic proteins that comprise a large family of E3 ubiquitin protein ligases. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jan 2011]","start":129634604,"end":129642169,"strand":-1,"description":"ankyrin repeat and SOCS box containing 6 [Source:HGNC Symbol;Acc:HGNC:17181]"}, {"versioned_ensembl_gene_id":"ENSG00000255286.2","gene_symbol":"AP000907.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111945639,"end":111946892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255334.1","gene_symbol":"AP000907.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":112015307,"end":112016124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266970.1","gene_symbol":"AC061992.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78360453,"end":78373911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227617.8","gene_symbol":"CERS6-AS1","gene_name":"CERS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44485]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100861402","summary":null,"start":168771953,"end":168786961,"strand":-1,"description":"CERS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44485]"}, {"versioned_ensembl_gene_id":"ENSG00000184557.4","gene_symbol":"SOCS3","gene_name":"suppressor of cytokine signaling 3 [Source:HGNC Symbol;Acc:HGNC:19391]","synonyms":"SSI-3,SOCS-3,Cish3,CIS3","biotype":"protein_coding","ncbi_id":"9021","summary":"This gene encodes a member of the STAT-induced STAT inhibitor (SSI), also known as suppressor of cytokine signaling (SOCS), family. SSI family members are cytokine-inducible negative regulators of cytokine signaling. The expression of this gene is induced by various cytokines, including IL6, IL10, and interferon (IFN)-gamma. The protein encoded by this gene can bind to JAK2 kinase, and inhibit the activity of JAK2 kinase. Studies of the mouse counterpart of this gene suggested the roles of this gene in the negative regulation of fetal liver hematopoiesis, and placental development. [provided by RefSeq, Jul 2008]","start":78356778,"end":78360077,"strand":-1,"description":"suppressor of cytokine signaling 3 [Source:HGNC Symbol;Acc:HGNC:19391]"}, {"versioned_ensembl_gene_id":"ENSG00000224286.5","gene_symbol":"LINC01142","gene_name":"long intergenic non-protein coding RNA 1142 [Source:HGNC Symbol;Acc:HGNC:49456]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284688","summary":null,"start":170271603,"end":170284208,"strand":-1,"description":"long intergenic non-protein coding RNA 1142 [Source:HGNC Symbol;Acc:HGNC:49456]"}, {"versioned_ensembl_gene_id":"ENSG00000248350.1","gene_symbol":"AC010265.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112363456,"end":112363666,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154096.13","gene_symbol":"THY1","gene_name":"Thy-1 cell surface antigen [Source:HGNC Symbol;Acc:HGNC:11801]","synonyms":"CD90","biotype":"protein_coding","ncbi_id":"7070","summary":"This gene encodes a cell surface glycoprotein and member of the immunoglobulin superfamily of proteins. The encoded protein is involved in cell adhesion and cell communication in numerous cell types, but particularly in cells of the immune and nervous systems. The encoded protein is widely used as a marker for hematopoietic stem cells. This gene may function as a tumor suppressor in nasopharyngeal carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":119417378,"end":119424985,"strand":-1,"description":"Thy-1 cell surface antigen [Source:HGNC Symbol;Acc:HGNC:11801]"}, {"versioned_ensembl_gene_id":"ENSG00000279197.1","gene_symbol":"AC010608.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133574829,"end":133575298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249541.1","gene_symbol":"AC116359.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2787451,"end":2788549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112773.15","gene_symbol":"FAM46A","gene_name":"family with sequence similarity 46 member A [Source:HGNC Symbol;Acc:HGNC:18345]","synonyms":"FLJ20037,C6orf37","biotype":"protein_coding","ncbi_id":"55603","summary":null,"start":81491439,"end":81752774,"strand":-1,"description":"family with sequence similarity 46 member A [Source:HGNC Symbol;Acc:HGNC:18345]"}, {"versioned_ensembl_gene_id":"ENSG00000130347.12","gene_symbol":"RTN4IP1","gene_name":"reticulon 4 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18647]","synonyms":"NIMP","biotype":"protein_coding","ncbi_id":"84816","summary":"This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, cognitive disability, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":106571971,"end":106629487,"strand":-1,"description":"reticulon 4 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18647]"}, {"versioned_ensembl_gene_id":"ENSG00000072134.15","gene_symbol":"EPN2","gene_name":"epsin 2 [Source:HGNC Symbol;Acc:HGNC:18639]","synonyms":"KIAA1065,EHB21","biotype":"protein_coding","ncbi_id":"22905","summary":"This gene encodes a protein which interacts with clathrin and adaptor-related protein complex 2, alpha 1 subunit. The protein is found in a brain-derived clathrin-coated vesicle fraction and localizes to the peri-Golgi region and the cell periphery. The protein is thought to be involved in clathrin-mediated endocytosis. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":19215615,"end":19336715,"strand":1,"description":"epsin 2 [Source:HGNC Symbol;Acc:HGNC:18639]"}, {"versioned_ensembl_gene_id":"ENSG00000186094.16","gene_symbol":"AGBL4","gene_name":"ATP/GTP binding protein like 4 [Source:HGNC Symbol;Acc:HGNC:25892]","synonyms":"FLJ14442,CCP6","biotype":"protein_coding","ncbi_id":"84871","summary":null,"start":48532855,"end":50023913,"strand":-1,"description":"ATP/GTP binding protein like 4 [Source:HGNC Symbol;Acc:HGNC:25892]"}, {"versioned_ensembl_gene_id":"ENSG00000265263.1","gene_symbol":"AC124066.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19334308,"end":19336127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170561.12","gene_symbol":"IRX2","gene_name":"iroquois homeobox 2 [Source:HGNC Symbol;Acc:HGNC:14359]","synonyms":null,"biotype":"protein_coding","ncbi_id":"153572","summary":"IRX2 is a member of the Iroquois homeobox gene family. Members of this family appear to play multiple roles during pattern formation of vertebrate embryos.[supplied by OMIM, Apr 2004]","start":2745845,"end":2751662,"strand":-1,"description":"iroquois homeobox 2 [Source:HGNC Symbol;Acc:HGNC:14359]"}, {"versioned_ensembl_gene_id":"ENSG00000283288.1","gene_symbol":"AC138517.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":139470778,"end":139474772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145331.13","gene_symbol":"TRMT10A","gene_name":"tRNA methyltransferase 10A [Source:HGNC Symbol;Acc:HGNC:28403]","synonyms":"TRM10,RG9MTD2,MGC27034","biotype":"protein_coding","ncbi_id":"93587","summary":"This gene encodes a protein that belongs to the tRNA (Guanine-1)-methyltransferase family. A similar gene in yeast modifies several different tRNA species. Mutations in this gene are associated with microcephaly, short stature, and impaired glucose metabolism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":99546709,"end":99564032,"strand":-1,"description":"tRNA methyltransferase 10A [Source:HGNC Symbol;Acc:HGNC:28403]"}, {"versioned_ensembl_gene_id":"ENSG00000254445.1","gene_symbol":"HSPB2-C11orf52","gene_name":"HSPB2-C11orf52 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528019","summary":"This locus represents naturally occurring read-through transcription between the neighboring heat shock 27kDa protein 2 (HSPB2) and chromosome 11 open reading frame 52 (C11orf52) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD) based on the use of the supported HSPB2 translational start codon, and it is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":111912736,"end":111926871,"strand":1,"description":"HSPB2-C11orf52 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41996]"}, {"versioned_ensembl_gene_id":"ENSG00000276478.1","gene_symbol":"AL772337.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87799501,"end":87821803,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232743.2","gene_symbol":"ELF2P3","gene_name":"E74-like factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:24611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"260336","summary":null,"start":87816465,"end":87817970,"strand":1,"description":"E74-like factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:24611]"}, {"versioned_ensembl_gene_id":"ENSG00000170606.14","gene_symbol":"HSPA4","gene_name":"heat shock protein family A (Hsp70) member 4 [Source:HGNC Symbol;Acc:HGNC:5237]","synonyms":"HSPH2,HS24/P52","biotype":"protein_coding","ncbi_id":"3308","summary":null,"start":133051962,"end":133106449,"strand":1,"description":"heat shock protein family A (Hsp70) member 4 [Source:HGNC Symbol;Acc:HGNC:5237]"}, {"versioned_ensembl_gene_id":"ENSG00000255855.2","gene_symbol":"KDM4F","gene_name":"lysine demethylase 4F [Source:HGNC Symbol;Acc:HGNC:52413]","synonyms":"JMJD2F","biotype":"protein_coding","ncbi_id":"100129053","summary":null,"start":95049422,"end":95051338,"strand":1,"description":"lysine demethylase 4F [Source:HGNC Symbol;Acc:HGNC:52413]"}, {"versioned_ensembl_gene_id":"ENSG00000269242.1","gene_symbol":"AC010422.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12643831,"end":12648397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120088.14","gene_symbol":"CRHR1","gene_name":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]","synonyms":"CRF-R,CRHR,CRF1,CRF-R,CRHR,CRF1","biotype":"protein_coding","ncbi_id":"1394","summary":"This gene encodes a G-protein coupled receptor that binds neuropeptides of the corticotropin releasing hormone family that are major regulators of the hypothalamic-pituitary-adrenal pathway. The encoded protein is essential for the activation of signal transduction pathways that regulate diverse physiological processes including stress, reproduction, immune response and obesity. Alternative splicing results in multiple transcript variants. Naturally-occurring readthrough transcription between this gene and upstream GeneID:147081 results in transcripts that encode isoforms that share similarity with the products of this gene. [provided by RefSeq, Aug 2016]","start":45784280,"end":45835828,"strand":1,"description":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]"}, {"versioned_ensembl_gene_id":"ENSG00000261347.1","gene_symbol":"AP000439.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69467598,"end":69469705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272023.1","gene_symbol":"AC010240.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132963770,"end":132964164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255980.1","gene_symbol":"AP000439.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69425690,"end":69429621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219297.1","gene_symbol":"MRPL42P3","gene_name":"mitochondrial ribosomal protein L42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29712]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359746","summary":null,"start":144136450,"end":144136775,"strand":1,"description":"mitochondrial ribosomal protein L42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29712]"}, {"versioned_ensembl_gene_id":"ENSG00000213525.3","gene_symbol":"AL357037.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74744386,"end":74744707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217767.2","gene_symbol":"NDUFAB1P1","gene_name":"NADH:ubiquinone oxidoreductase subunit AB1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52265]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075303","summary":null,"start":70734503,"end":70734962,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit AB1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52265]"}, {"versioned_ensembl_gene_id":"ENSG00000271313.1","gene_symbol":"AC069114.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71932493,"end":71932796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265946.1","gene_symbol":"AC090312.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71665148,"end":71665525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265352.1","gene_symbol":"LINC01899","gene_name":"long intergenic non-protein coding RNA 1899 [Source:HGNC Symbol;Acc:HGNC:52718]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724913","summary":null,"start":71732615,"end":71788128,"strand":-1,"description":"long intergenic non-protein coding RNA 1899 [Source:HGNC Symbol;Acc:HGNC:52718]"}, {"versioned_ensembl_gene_id":"ENSG00000112305.14","gene_symbol":"SMAP1","gene_name":"small ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:19651]","synonyms":"SMAP-1,FLJ13159","biotype":"protein_coding","ncbi_id":"60682","summary":"The protein encoded by this gene is similar to the mouse stromal membrane-associated protein-1. This similarity suggests that this human gene product is also a type II membrane glycoprotein involved in the erythropoietic stimulatory activity of stromal cells. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":70667776,"end":70862015,"strand":1,"description":"small ArfGAP 1 [Source:HGNC Symbol;Acc:HGNC:19651]"}, {"versioned_ensembl_gene_id":"ENSG00000229622.1","gene_symbol":"MTND5P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873209","summary":null,"start":95692538,"end":95693972,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41919]"}, {"versioned_ensembl_gene_id":"ENSG00000234912.11","gene_symbol":"SNHG20","gene_name":"small nucleolar RNA host gene 20 [Source:HGNC Symbol;Acc:HGNC:33099]","synonyms":"SCARNA16HG,PRO0872,NCRNA00338,LINC00338,FLJ25582,DKFZp686L05235,C17orf86","biotype":"processed_transcript","ncbi_id":"654434","summary":null,"start":77086716,"end":77094990,"strand":1,"description":"small nucleolar RNA host gene 20 [Source:HGNC Symbol;Acc:HGNC:33099]"}, {"versioned_ensembl_gene_id":"ENSG00000072609.17","gene_symbol":"CHFR","gene_name":"checkpoint with forkhead and ring finger domains [Source:HGNC Symbol;Acc:HGNC:20455]","synonyms":"RNF196,FLJ10796","biotype":"protein_coding","ncbi_id":"55743","summary":"This gene encodes an E3 ubiquitin-protein ligase required for the maintenance of the antephase checkpoint that regulates cell cycle entry into mitosis and, therefore, may play a key role in cell cycle progression and tumorigenesis. The encoded protein has an N-terminal forkhead-associated domain, a central RING-finger domain, and a cysteine-rich C-terminal region. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Mar 2014]","start":132822187,"end":132956304,"strand":-1,"description":"checkpoint with forkhead and ring finger domains [Source:HGNC Symbol;Acc:HGNC:20455]"}, {"versioned_ensembl_gene_id":"ENSG00000250790.4","gene_symbol":"AC127070.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132911470,"end":132914732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258412.1","gene_symbol":"AL355102.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":96210860,"end":96214818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250124.1","gene_symbol":"AC016550.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86380660,"end":86381426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260259.1","gene_symbol":"LINC02166","gene_name":"long intergenic non-protein coding RNA 2166 [Source:HGNC Symbol;Acc:HGNC:53027]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371416","summary":null,"start":89682620,"end":89686569,"strand":-1,"description":"long intergenic non-protein coding RNA 2166 [Source:HGNC Symbol;Acc:HGNC:53027]"}, {"versioned_ensembl_gene_id":"ENSG00000254130.1","gene_symbol":"LINC01947","gene_name":"long intergenic non-protein coding RNA 1947 [Source:HGNC Symbol;Acc:HGNC:52771]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102557615","summary":null,"start":166905222,"end":166926370,"strand":-1,"description":"long intergenic non-protein coding RNA 1947 [Source:HGNC Symbol;Acc:HGNC:52771]"}, {"versioned_ensembl_gene_id":"ENSG00000165617.14","gene_symbol":"DACT1","gene_name":"dishevelled binding antagonist of beta catenin 1 [Source:HGNC Symbol;Acc:HGNC:17748]","synonyms":"THYEX3,HDPR1,FRODO,DAPPER1,DAPPER","biotype":"protein_coding","ncbi_id":"51339","summary":"The protein encoded by this gene belongs to the dapper family, characterized by the presence of PDZ-binding motif at the C-terminus. It interacts with, and positively regulates dishevelled-mediated signaling pathways during development. Depletion of this mRNA from xenopus embryos resulted in loss of notochord and head structures, and mice lacking this gene died shortly after birth from severe posterior malformations. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":58633967,"end":58648321,"strand":1,"description":"dishevelled binding antagonist of beta catenin 1 [Source:HGNC Symbol;Acc:HGNC:17748]"}, {"versioned_ensembl_gene_id":"ENSG00000100865.14","gene_symbol":"CINP","gene_name":"cyclin dependent kinase 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:23789]","synonyms":"MGC849","biotype":"protein_coding","ncbi_id":"51550","summary":"The protein encoded by this gene is reported to be a component of the DNA replication complex as well as a genome-maintenance protein. It may interact with proteins important for replication initiation and has been shown to bind chromatin at the G1 phase of the cell cycle and dissociate from chromatin with replication initiation. It may also serve to regulate checkpoint signaling as part of the DNA damage response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":102341102,"end":102362916,"strand":-1,"description":"cyclin dependent kinase 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:23789]"}, {"versioned_ensembl_gene_id":"ENSG00000136504.11","gene_symbol":"KAT7","gene_name":"lysine acetyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:17016]","synonyms":"HBO1,ZC2HC7,MYST2,HBOA","biotype":"protein_coding","ncbi_id":"11143","summary":"The protein encoded by this gene is part of the multimeric HBO1 complex, which possesses histone H4-specific acetyltransferase activity. This activity is required for functional replication origins and is involved in transcriptional activation of some genes. In both cases, the acetylation of histone H4 helps unfold chromatin so that the DNA can be accessed and replicated or transcribed. [provided by RefSeq, Oct 2016]","start":49788555,"end":49835030,"strand":1,"description":"lysine acetyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:17016]"}, {"versioned_ensembl_gene_id":"ENSG00000279063.1","gene_symbol":"AC008735.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":55467438,"end":55467934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279872.1","gene_symbol":"AC006435.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2424179,"end":2424412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283567.1","gene_symbol":"AC008735.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55463002,"end":55464707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254289.2","gene_symbol":"IGHV3-32","gene_name":"immunoglobulin heavy variable 3-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5595]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28435","summary":null,"start":106331106,"end":106331563,"strand":-1,"description":"immunoglobulin heavy variable 3-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5595]"}, {"versioned_ensembl_gene_id":"ENSG00000072364.12","gene_symbol":"AFF4","gene_name":"AF4/FMR2 family member 4 [Source:HGNC Symbol;Acc:HGNC:17869]","synonyms":"MCEF,AF5Q31","biotype":"protein_coding","ncbi_id":"27125","summary":"The protein encoded by this gene belongs to the AF4 family of transcription factors involved in leukemia. It is a component of the positive transcription elongation factor b (P-TEFb) complex. A chromosomal translocation involving this gene and MLL gene on chromosome 11 is found in infant acute lymphoblastic leukemia with ins(5;11)(q31;q31q23). [provided by RefSeq, Oct 2011]","start":132875379,"end":132963634,"strand":-1,"description":"AF4/FMR2 family member 4 [Source:HGNC Symbol;Acc:HGNC:17869]"}, {"versioned_ensembl_gene_id":"ENSG00000226253.1","gene_symbol":"MRPL35P3","gene_name":"mitochondrial ribosomal protein L35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23731]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359744","summary":null,"start":74527584,"end":74527947,"strand":1,"description":"mitochondrial ribosomal protein L35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23731]"}, {"versioned_ensembl_gene_id":"ENSG00000271710.1","gene_symbol":"NDUFA8P1","gene_name":"NADH:ubiquinone oxidoreductase subunit A8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52264]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075207","summary":null,"start":74641410,"end":74641776,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52264]"}, {"versioned_ensembl_gene_id":"ENSG00000197050.10","gene_symbol":"ZNF420","gene_name":"zinc finger protein 420 [Source:HGNC Symbol;Acc:HGNC:20649]","synonyms":"FLJ32191","biotype":"protein_coding","ncbi_id":"147923","summary":"The protein encoded by this gene is a KRAB-type zinc finger protein that negatively-regulates p53-mediated apoptosis. Under stress conditions, the encoded protein is phosphorylated by ATM and dissociates from p53, which activates p53 and initiates apoptosis. [provided by RefSeq, Jul 2016]","start":37007857,"end":37130314,"strand":1,"description":"zinc finger protein 420 [Source:HGNC Symbol;Acc:HGNC:20649]"}, {"versioned_ensembl_gene_id":"ENSG00000249423.1","gene_symbol":"AC109464.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124919947,"end":124921598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166025.17","gene_symbol":"AMOTL1","gene_name":"angiomotin like 1 [Source:HGNC Symbol;Acc:HGNC:17811]","synonyms":"JEAP","biotype":"protein_coding","ncbi_id":"154810","summary":"The protein encoded by this gene is a peripheral membrane protein that is a component of tight junctions or TJs. TJs form an apical junctional structure and act to control paracellular permeability and maintain cell polarity. This protein is related to angiomotin, an angiostatin binding protein that regulates endothelial cell migration and capillary formation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":94706431,"end":94876753,"strand":1,"description":"angiomotin like 1 [Source:HGNC Symbol;Acc:HGNC:17811]"}, {"versioned_ensembl_gene_id":"ENSG00000271171.1","gene_symbol":"AC008555.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34904392,"end":34905057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249261.1","gene_symbol":"AC109464.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124868972,"end":124869914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270544.1","gene_symbol":"AC008555.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34902202,"end":34904195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248443.1","gene_symbol":"AC109464.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124829472,"end":124830290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211978.2","gene_symbol":"IGHV5-78","gene_name":"immunoglobulin heavy variable 5-78 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5660]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28387","summary":null,"start":106851123,"end":106851417,"strand":-1,"description":"immunoglobulin heavy variable 5-78 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5660]"}, {"versioned_ensembl_gene_id":"ENSG00000263934.4","gene_symbol":"SNORD3A","gene_name":"small nucleolar RNA, C/D box 3A [Source:HGNC Symbol;Acc:HGNC:33189]","synonyms":"U3,RNU3","biotype":"snoRNA","ncbi_id":"780851","summary":"U3 RNA, an abundant small nucleolar RNA (snoRNA), is thought to play a role in the processing of ribosomal RNA precursors (Bernstein et al., 1983 [PubMed 6186397]).[supplied by OMIM, Jun 2009]","start":19188016,"end":19188714,"strand":1,"description":"small nucleolar RNA, C/D box 3A [Source:HGNC Symbol;Acc:HGNC:33189]"}, {"versioned_ensembl_gene_id":"ENSG00000141741.11","gene_symbol":"MIEN1","gene_name":"migration and invasion enhancer 1 [Source:HGNC Symbol;Acc:HGNC:28230]","synonyms":"MGC14832,C35,C17orf37,XTP4,Rdx12,ORB3","biotype":"protein_coding","ncbi_id":"84299","summary":null,"start":39728496,"end":39730787,"strand":-1,"description":"migration and invasion enhancer 1 [Source:HGNC Symbol;Acc:HGNC:28230]"}, {"versioned_ensembl_gene_id":"ENSG00000278173.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54853492,"end":54877496,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000267604.1","gene_symbol":"AC003098.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43782804,"end":43784682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274576.2","gene_symbol":"IGHV2-70","gene_name":"immunoglobulin heavy variable 2-70 [Source:HGNC Symbol;Acc:HGNC:5577]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28454","summary":null,"start":106770577,"end":106771020,"strand":-1,"description":"immunoglobulin heavy variable 2-70 [Source:HGNC Symbol;Acc:HGNC:5577]"}, {"versioned_ensembl_gene_id":"ENSG00000254056.1","gene_symbol":"IGHV3-71","gene_name":"immunoglobulin heavy variable 3-71 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5621]","synonyms":"IGHV3-G","biotype":"IG_V_pseudogene","ncbi_id":"28411","summary":null,"start":106775157,"end":106775618,"strand":-1,"description":"immunoglobulin heavy variable 3-71 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5621]"}, {"versioned_ensembl_gene_id":"ENSG00000211974.3","gene_symbol":"AC245369.1","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106723574,"end":106724093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263417.4","gene_symbol":"GTSCR1","gene_name":"Gilles de la Tourette syndrome chromosome region, candidate 1 [Source:HGNC Symbol;Acc:HGNC:18406]","synonyms":null,"biotype":"lincRNA","ncbi_id":"220158","summary":null,"start":70630534,"end":70650744,"strand":-1,"description":"Gilles de la Tourette syndrome chromosome region, candidate 1 [Source:HGNC Symbol;Acc:HGNC:18406]"}, {"versioned_ensembl_gene_id":"ENSG00000206465.4","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":30920912,"end":30921734,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000144579.7","gene_symbol":"CTDSP1","gene_name":"CTD small phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:21614]","synonyms":"SCP1,NLIIF","biotype":"protein_coding","ncbi_id":"58190","summary":"This gene encodes a member of the small C-terminal domain phosphatase (SCP) family of nuclear phosphatases. These proteins play a role in transcriptional regulation through specific dephosphorylation of phosphoserine 5 within tandem heptapeptide repeats of the C-terminal domain of RNA polymerase II. The encoded protein plays a role in neuronal gene silencing in non-neuronal cells, and may also inhibit osteoblast differentiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":218398256,"end":218405941,"strand":1,"description":"CTD small phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:21614]"}, {"versioned_ensembl_gene_id":"ENSG00000161395.13","gene_symbol":"PGAP3","gene_name":"post-GPI attachment to proteins 3 [Source:HGNC Symbol;Acc:HGNC:23719]","synonyms":"PP1498,PERLD1,PER1,MGC9753,CAB2","biotype":"protein_coding","ncbi_id":"93210","summary":"This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]","start":39671122,"end":39696797,"strand":-1,"description":"post-GPI attachment to proteins 3 [Source:HGNC Symbol;Acc:HGNC:23719]"}, {"versioned_ensembl_gene_id":"ENSG00000284526.1","gene_symbol":"AC015802.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76563710,"end":76570544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225438.1","gene_symbol":"KRT41P","gene_name":"keratin 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:6457]","synonyms":"phihHaA,KRTHAP1,HHaA","biotype":"unprocessed_pseudogene","ncbi_id":"8686","summary":null,"start":41406512,"end":41411775,"strand":-1,"description":"keratin 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:6457]"}, {"versioned_ensembl_gene_id":"ENSG00000233348.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31629769,"end":31643448,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000267078.1","gene_symbol":"AC015802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76569792,"end":76571240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070731.10","gene_symbol":"ST6GALNAC2","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10867]","synonyms":"STHM,ST6GalNAII,SIATL1,SIAT7B,SIAT7","biotype":"protein_coding","ncbi_id":"10610","summary":"ST6GALNAC2 belongs to a family of sialyltransferases that add sialic acids to the nonreducing ends of glycoconjugates. At the cell surface, these modifications have roles in cell-cell and cell-substrate interactions, bacterial adhesion, and protein targeting (Samyn-Petit et al., 2000 [PubMed 10742600]).[supplied by OMIM, Mar 2008]","start":76565379,"end":76586956,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10867]"}, {"versioned_ensembl_gene_id":"ENSG00000074219.13","gene_symbol":"TEAD2","gene_name":"TEA domain transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11715]","synonyms":"TEF4,TEF-4,ETF","biotype":"protein_coding","ncbi_id":"8463","summary":null,"start":49340595,"end":49362457,"strand":-1,"description":"TEA domain transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11715]"}, {"versioned_ensembl_gene_id":"ENSG00000196730.12","gene_symbol":"DAPK1","gene_name":"death associated protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:2674]","synonyms":"ROCO3,DAPK","biotype":"protein_coding","ncbi_id":"1612","summary":"Death-associated protein kinase 1 is a positive mediator of gamma-interferon induced programmed cell death. DAPK1 encodes a structurally unique 160-kD calmodulin dependent serine-threonine kinase that carries 8 ankyrin repeats and 2 putative P-loop consensus sites. It is a tumor suppressor candidate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":87497228,"end":87708633,"strand":1,"description":"death associated protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:2674]"}, {"versioned_ensembl_gene_id":"ENSG00000276424.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,nkat4a,CD158K","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54895138,"end":54911932,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000160013.8","gene_symbol":"PTGIR","gene_name":"prostaglandin I2 (prostacyclin) receptor (IP) [Source:HGNC Symbol;Acc:HGNC:9602]","synonyms":"IP","biotype":"protein_coding","ncbi_id":"5739","summary":"The protein encoded by this gene is a member of the G-protein coupled receptor family 1 and has been shown to be a receptor for prostacyclin. Prostacyclin, the major product of cyclooxygenase in macrovascular endothelium, elicits a potent vasodilation and inhibition of platelet aggregation through binding to this receptor. [provided by RefSeq, Jul 2008]","start":46620468,"end":46625118,"strand":-1,"description":"prostaglandin I2 (prostacyclin) receptor (IP) [Source:HGNC Symbol;Acc:HGNC:9602]"}, {"versioned_ensembl_gene_id":"ENSG00000273111.5","gene_symbol":"LYPD4","gene_name":"LY6/PLAUR domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28659]","synonyms":"MGC42718","biotype":"protein_coding","ncbi_id":"147719","summary":null,"start":41837074,"end":41844697,"strand":-1,"description":"LY6/PLAUR domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28659]"}, {"versioned_ensembl_gene_id":"ENSG00000213290.4","gene_symbol":"PGK1P2","gene_name":"phosphoglycerate kinase 1, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8899]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5233","summary":null,"start":12559571,"end":12561105,"strand":1,"description":"phosphoglycerate kinase 1, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8899]"}, {"versioned_ensembl_gene_id":"ENSG00000248406.1","gene_symbol":"AC008758.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12379746,"end":12383687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196634.3","gene_symbol":"LUADT1","gene_name":"lung adenocarcinoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:51845]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106182249","summary":null,"start":147158925,"end":147180992,"strand":1,"description":"lung adenocarcinoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:51845]"}, {"versioned_ensembl_gene_id":"ENSG00000254990.5","gene_symbol":"AP001781.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111768668,"end":111778350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151176.7","gene_symbol":"PLBD2","gene_name":"phospholipase B domain containing 2 [Source:HGNC Symbol;Acc:HGNC:27283]","synonyms":"p76","biotype":"protein_coding","ncbi_id":"196463","summary":null,"start":113358566,"end":113391625,"strand":1,"description":"phospholipase B domain containing 2 [Source:HGNC Symbol;Acc:HGNC:27283]"}, {"versioned_ensembl_gene_id":"ENSG00000284713.1","gene_symbol":"AP003071.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69155478,"end":69159752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250438.1","gene_symbol":"AC025465.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124469591,"end":124469901,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232292.1","gene_symbol":"ALDH7A1P2","gene_name":"aldehyde dehydrogenase 7 family member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:879]","synonyms":"ATQL2","biotype":"processed_pseudogene","ncbi_id":"542","summary":null,"start":172893763,"end":172894383,"strand":-1,"description":"aldehyde dehydrogenase 7 family member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:879]"}, {"versioned_ensembl_gene_id":"ENSG00000249439.1","gene_symbol":"HMGN1P14","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39358]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874440","summary":null,"start":111846050,"end":111846566,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39358]"}, {"versioned_ensembl_gene_id":"ENSG00000249619.1","gene_symbol":"HMGN1P13","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874439","summary":null,"start":111572102,"end":111572239,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39357]"}, {"versioned_ensembl_gene_id":"ENSG00000257520.1","gene_symbol":"SFTA3","gene_name":"surfactant associated 3 [Source:NCBI gene;Acc:253970]","synonyms":"SP-H,SFTPH,NANCI,SFTPH,NANCI","biotype":"processed_transcript","ncbi_id":"253970","summary":null,"start":36473207,"end":36519521,"strand":-1,"description":"surfactant associated 3 [Source:NCBI gene;Acc:253970]"}, {"versioned_ensembl_gene_id":"ENSG00000266278.1","gene_symbol":"LINC01910","gene_name":"long intergenic non-protein coding RNA 1910 [Source:HGNC Symbol;Acc:HGNC:52729]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060542","summary":null,"start":70380140,"end":70384591,"strand":-1,"description":"long intergenic non-protein coding RNA 1910 [Source:HGNC Symbol;Acc:HGNC:52729]"}, {"versioned_ensembl_gene_id":"ENSG00000026652.13","gene_symbol":"AGPAT4","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:20885]","synonyms":"LPAAT-delta,dJ473J16.2","biotype":"protein_coding","ncbi_id":"56895","summary":"This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. This integral membrane protein converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. [provided by RefSeq, Jul 2008]","start":161129979,"end":161274061,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:20885]"}, {"versioned_ensembl_gene_id":"ENSG00000259834.1","gene_symbol":"AL365361.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110653560,"end":110657040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162341.16","gene_symbol":"TPCN2","gene_name":"two pore segment channel 2 [Source:HGNC Symbol;Acc:HGNC:20820]","synonyms":"TPC2","biotype":"protein_coding","ncbi_id":"219931","summary":"This gene encodes a putative cation-selective ion channel with two repeats of a six-transmembrane-domain. The protein localizes to lysosomal membranes and enables nicotinic acid adenine dinucleotide phosphate (NAADP) -induced calcium ion release from lysosome-related stores. This ubiquitously expressed gene has elevated expression in liver and kidney. Two common nonsynonymous SNPs in this gene strongly associate with blond versus brown hair pigmentation.[provided by RefSeq, Dec 2009]","start":69048897,"end":69162440,"strand":1,"description":"two pore segment channel 2 [Source:HGNC Symbol;Acc:HGNC:20820]"}, {"versioned_ensembl_gene_id":"ENSG00000176170.13","gene_symbol":"SPHK1","gene_name":"sphingosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:11240]","synonyms":"SPHK","biotype":"protein_coding","ncbi_id":"8877","summary":"The protein encoded by this gene catalyzes the phosphorylation of sphingosine to form sphingosine-1-phosphate (S1P), a lipid mediator with both intra- and extracellular functions. Intracellularly, S1P regulates proliferation and survival, and extracellularly, it is a ligand for cell surface G protein-coupled receptors. This protein, and its product S1P, play a key role in TNF-alpha signaling and the NF-kappa-B activation pathway important in inflammatory, antiapoptotic, and immune processes. Phosphorylation of this protein alters its catalytic activity and promotes its translocation to the plasma membrane. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2017]","start":76376584,"end":76387860,"strand":1,"description":"sphingosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:11240]"}, {"versioned_ensembl_gene_id":"ENSG00000170677.5","gene_symbol":"SOCS6","gene_name":"suppressor of cytokine signaling 6 [Source:HGNC Symbol;Acc:HGNC:16833]","synonyms":"STATI4,STAI4,SSI4,SOCS4,HSPC060,Cish4,CIS4","biotype":"protein_coding","ncbi_id":"9306","summary":"The protein encoded by this gene contains a SH2 domain and a CIS homolog domain. The protein thus belongs to the cytokine-induced STAT inhibitor (CIS), also known as suppressor of cytokine signaling (SOCS) or STAT-induced STAT inhibitor (SSI), protein family. CIS family members are known to be cytokine-inducible negative regulators of cytokine signaling. The expression of this gene can be induced by GM-CSF and EPO in hematopoietic cells. A high expression level of this gene was found in factor-independent chronic myelogenous leukemia (CML) and erythroleukemia (HEL) cell lines. [provided by RefSeq, Jul 2008]","start":70288901,"end":70330200,"strand":1,"description":"suppressor of cytokine signaling 6 [Source:HGNC Symbol;Acc:HGNC:16833]"}, {"versioned_ensembl_gene_id":"ENSG00000035403.17","gene_symbol":"VCL","gene_name":"vinculin [Source:HGNC Symbol;Acc:HGNC:12665]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7414","summary":"Vinculin is a cytoskeletal protein associated with cell-cell and cell-matrix junctions, where it is thought to function as one of several interacting proteins involved in anchoring F-actin to the membrane. Defects in VCL are the cause of cardiomyopathy dilated type 1W. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":73995193,"end":74121363,"strand":1,"description":"vinculin [Source:HGNC Symbol;Acc:HGNC:12665]"}, {"versioned_ensembl_gene_id":"ENSG00000198807.12","gene_symbol":"PAX9","gene_name":"paired box 9 [Source:HGNC Symbol;Acc:HGNC:8623]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5083","summary":"This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. Mice lacking this gene exhibit impaired development of organs, musculature and the skeleton, including absent and abnormally developed teeth, and neonatal lethality. Mutations in the human gene are associated with selective tooth agenesis-3. [provided by RefSeq, Sep 2015]","start":36657568,"end":36679715,"strand":1,"description":"paired box 9 [Source:HGNC Symbol;Acc:HGNC:8623]"}, {"versioned_ensembl_gene_id":"ENSG00000232615.4","gene_symbol":"AC026412.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1614836,"end":1616334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063127.15","gene_symbol":"SLC6A16","gene_name":"solute carrier family 6 member 16 [Source:HGNC Symbol;Acc:HGNC:13622]","synonyms":"NTT5","biotype":"protein_coding","ncbi_id":"28968","summary":"SLC6A16 shows structural characteristics of an Na(+)- and Cl(-)-dependent neurotransmitter transporter, including 12 transmembrane (TM) domains, intracellular N and C termini, and large extracellular loops containing multiple N-glycosylation sites.[supplied by OMIM, Mar 2008]","start":49289638,"end":49325225,"strand":-1,"description":"solute carrier family 6 member 16 [Source:HGNC Symbol;Acc:HGNC:13622]"}, {"versioned_ensembl_gene_id":"ENSG00000226133.6","gene_symbol":"AL356289.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48050659,"end":48091736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274150.1","gene_symbol":"FADS2P1","gene_name":"fatty acid desaturase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43618]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643181","summary":null,"start":56890613,"end":56927885,"strand":1,"description":"fatty acid desaturase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43618]"}, {"versioned_ensembl_gene_id":"ENSG00000237888.1","gene_symbol":"AC087650.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43476198,"end":43476665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269113.3","gene_symbol":"TRABD2B","gene_name":"TraB domain containing 2B [Source:HGNC Symbol;Acc:HGNC:44200]","synonyms":"TIKI2","biotype":"protein_coding","ncbi_id":"388630","summary":null,"start":47760528,"end":47996895,"strand":-1,"description":"TraB domain containing 2B [Source:HGNC Symbol;Acc:HGNC:44200]"}, {"versioned_ensembl_gene_id":"ENSG00000225028.1","gene_symbol":"AC096541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47818066,"end":47820237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237415.2","gene_symbol":"NRBF2P3","gene_name":"nuclear receptor binding factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44606]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643232","summary":null,"start":110848077,"end":110848941,"strand":-1,"description":"nuclear receptor binding factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44606]"}, {"versioned_ensembl_gene_id":"ENSG00000270299.1","gene_symbol":"AL121758.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":646626,"end":675800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121067.17","gene_symbol":"SPOP","gene_name":"speckle type BTB/POZ protein [Source:HGNC Symbol;Acc:HGNC:11254]","synonyms":"TEF2,BTBD32","biotype":"protein_coding","ncbi_id":"8405","summary":"This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":49598884,"end":49678234,"strand":-1,"description":"speckle type BTB/POZ protein [Source:HGNC Symbol;Acc:HGNC:11254]"}, {"versioned_ensembl_gene_id":"ENSG00000227947.1","gene_symbol":"LINC01738","gene_name":"long intergenic non-protein coding RNA 1738 [Source:HGNC Symbol;Acc:HGNC:52526]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984953","summary":null,"start":47688463,"end":47703383,"strand":1,"description":"long intergenic non-protein coding RNA 1738 [Source:HGNC Symbol;Acc:HGNC:52526]"}, {"versioned_ensembl_gene_id":"ENSG00000260962.1","gene_symbol":"LINC00557","gene_name":"long intergenic non-protein coding RNA 557 [Source:HGNC Symbol;Acc:HGNC:43701]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861544","summary":null,"start":94960041,"end":94961319,"strand":1,"description":"long intergenic non-protein coding RNA 557 [Source:HGNC Symbol;Acc:HGNC:43701]"}, {"versioned_ensembl_gene_id":"ENSG00000125878.6","gene_symbol":"TCF15","gene_name":"transcription factor 15 [Source:HGNC Symbol;Acc:HGNC:11627]","synonyms":"PARAXIS,EC2,bHLHa40","biotype":"protein_coding","ncbi_id":"6939","summary":"The protein encoded by this gene is found in the nucleus and may be involved in the early transcriptional regulation of patterning of the mesoderm. The encoded basic helix-loop-helix protein requires dimerization with another basic helix-loop-helix protein for efficient DNA binding. [provided by RefSeq, Jul 2008]","start":603797,"end":610398,"strand":-1,"description":"transcription factor 15 [Source:HGNC Symbol;Acc:HGNC:11627]"}, {"versioned_ensembl_gene_id":"ENSG00000167380.16","gene_symbol":"ZNF226","gene_name":"zinc finger protein 226 [Source:HGNC Symbol;Acc:HGNC:13019]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7769","summary":null,"start":44165073,"end":44178381,"strand":1,"description":"zinc finger protein 226 [Source:HGNC Symbol;Acc:HGNC:13019]"}, {"versioned_ensembl_gene_id":"ENSG00000172457.6","gene_symbol":"OR9G4","gene_name":"olfactory receptor family 9 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:15322]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283189","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56741223,"end":56748697,"strand":-1,"description":"olfactory receptor family 9 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:15322]"}, {"versioned_ensembl_gene_id":"ENSG00000258012.1","gene_symbol":"AC026111.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92858079,"end":92859273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154978.12","gene_symbol":"VOPP1","gene_name":"vesicular, overexpressed in cancer, prosurvival protein 1 [Source:HGNC Symbol;Acc:HGNC:34518]","synonyms":"GASP,FLJ20532,ECop,DKFZp564K0822","biotype":"protein_coding","ncbi_id":"81552","summary":null,"start":55436056,"end":55572988,"strand":-1,"description":"vesicular, overexpressed in cancer, prosurvival protein 1 [Source:HGNC Symbol;Acc:HGNC:34518]"}, {"versioned_ensembl_gene_id":"ENSG00000261408.6","gene_symbol":"TEN1-CDK3","gene_name":"TEN1-CDK3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44420]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529145","summary":"This locus represents naturally occurring read-through transcription between the neighboring TEN1 telomerase capping complex subunit homolog (S. cerevisiae) and cyclin-dependent kinase 3 (CDK3) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Oct 2011]","start":75979231,"end":76005999,"strand":1,"description":"TEN1-CDK3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44420]"}, {"versioned_ensembl_gene_id":"ENSG00000114120.11","gene_symbol":"SLC25A36","gene_name":"solute carrier family 25 member 36 [Source:HGNC Symbol;Acc:HGNC:25554]","synonyms":"PNC2,FLJ10618","biotype":"protein_coding","ncbi_id":"55186","summary":null,"start":140941830,"end":140979933,"strand":1,"description":"solute carrier family 25 member 36 [Source:HGNC Symbol;Acc:HGNC:25554]"}, {"versioned_ensembl_gene_id":"ENSG00000188868.13","gene_symbol":"ZNF563","gene_name":"zinc finger protein 563 [Source:HGNC Symbol;Acc:HGNC:30498]","synonyms":"FLJ34797","biotype":"protein_coding","ncbi_id":"147837","summary":null,"start":12317477,"end":12333720,"strand":-1,"description":"zinc finger protein 563 [Source:HGNC Symbol;Acc:HGNC:30498]"}, {"versioned_ensembl_gene_id":"ENSG00000162368.13","gene_symbol":"CMPK1","gene_name":"cytidine/uridine monophosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:18170]","synonyms":"UMP-CMPK,CMPK","biotype":"protein_coding","ncbi_id":"51727","summary":"This gene encodes one of the enzymes required for cellular nucleic acid biosynthesis. This enzyme catalyzes the transfer of a phosphate group from ATP to CMP, UMP, or dCMP, to form the corresponding diphosphate nucleotide. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Feb 2012]","start":47333797,"end":47378839,"strand":1,"description":"cytidine/uridine monophosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:18170]"}, {"versioned_ensembl_gene_id":"ENSG00000236967.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"HZFw1,LIRF","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30062765,"end":30068386,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000128285.4","gene_symbol":"MCHR1","gene_name":"melanin concentrating hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:4479]","synonyms":"SLC1,MCH1R,GPR24","biotype":"protein_coding","ncbi_id":"2847","summary":"The protein encoded by this gene, a member of the G protein-coupled receptor family 1, is an integral plasma membrane protein which binds melanin-concentrating hormone. The encoded protein can inhibit cAMP accumulation and stimulate intracellular calcium flux, and is probably involved in the neuronal regulation of food consumption. Although structurally similar to somatostatin receptors, this protein does not seem to bind somatostatin. [provided by RefSeq, Jul 2008]","start":40678750,"end":40682814,"strand":1,"description":"melanin concentrating hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:4479]"}, {"versioned_ensembl_gene_id":"ENSG00000261826.1","gene_symbol":"AC121333.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140865075,"end":140867783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237567.1","gene_symbol":"Z97206.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105612667,"end":105632196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211950.2","gene_symbol":"IGHV1-24","gene_name":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28467","summary":null,"start":106276548,"end":106277043,"strand":-1,"description":"immunoglobulin heavy variable 1-24 [Source:HGNC Symbol;Acc:HGNC:5551]"}, {"versioned_ensembl_gene_id":"ENSG00000268400.5","gene_symbol":"AC008763.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7629796,"end":7643048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255931.1","gene_symbol":"AP003108.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61496440,"end":61500076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197102.10","gene_symbol":"DYNC1H1","gene_name":"dynein cytoplasmic 1 heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2961]","synonyms":"DHC1,CMT2O,p22,HL-3,DNECL,DNCL,Dnchc1,DNCH1","biotype":"protein_coding","ncbi_id":"1778","summary":"Dyneins are a group of microtubule-activated ATPases that function as molecular motors. They are divided into two subgroups of axonemal and cytoplasmic dyneins. The cytoplasmic dyneins function in intracellular motility, including retrograde axonal transport, protein sorting, organelle movement, and spindle dynamics. Molecules of conventional cytoplasmic dynein are comprised of 2 heavy chain polypeptides and a number of intermediate and light chains.This gene encodes a member of the cytoplasmic dynein heavy chain family. [provided by RefSeq, Oct 2008]","start":101964528,"end":102050792,"strand":1,"description":"dynein cytoplasmic 1 heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2961]"}, {"versioned_ensembl_gene_id":"ENSG00000243345.1","gene_symbol":"AC093714.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115789729,"end":115791049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258959.1","gene_symbol":"AL118558.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102036315,"end":102066228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248967.1","gene_symbol":"AC022493.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80746339,"end":80746819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258615.1","gene_symbol":"AL117187.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95199039,"end":95199345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177301.14","gene_symbol":"KCNA2","gene_name":"potassium voltage-gated channel subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:6220]","synonyms":"Kv1.2,HK4","biotype":"protein_coding","ncbi_id":"3737","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, members of which allow nerve cells to efficiently repolarize following an action potential. The coding region of this gene is intronless, and the gene is clustered with genes KCNA3 and KCNA10 on chromosome 1. [provided by RefSeq, Jul 2008]","start":110519837,"end":110631474,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:6220]"}, {"versioned_ensembl_gene_id":"ENSG00000232485.2","gene_symbol":"AC098820.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":216479030,"end":216498761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183018.8","gene_symbol":"SPNS2","gene_name":"sphingolipid transporter 2 [Source:HGNC Symbol;Acc:HGNC:26992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124976","summary":"The protein encoded by this gene is a transporter of sphingosine 1-phosphate, a secreted lipid that is important in cardiovascular, immunological, and neural development. Defects in this gene are a cause of early onset progressive hearing loss. [provided by RefSeq, Jul 2016]","start":4498838,"end":4539035,"strand":1,"description":"sphingolipid transporter 2 [Source:HGNC Symbol;Acc:HGNC:26992]"}, {"versioned_ensembl_gene_id":"ENSG00000100297.15","gene_symbol":"MCM5","gene_name":"minichromosome maintenance complex component 5 [Source:HGNC Symbol;Acc:HGNC:6948]","synonyms":"CDC46","biotype":"protein_coding","ncbi_id":"4174","summary":"The protein encoded by this gene is structurally very similar to the CDC46 protein from S. cerevisiae, a protein involved in the initiation of DNA replication. The encoded protein is a member of the MCM family of chromatin-binding proteins and can interact with at least two other members of this family. The encoded protein is upregulated in the transition from the G0 to G1/S phase of the cell cycle and may actively participate in cell cycle regulation. [provided by RefSeq, Jul 2008]","start":35400063,"end":35425430,"strand":1,"description":"minichromosome maintenance complex component 5 [Source:HGNC Symbol;Acc:HGNC:6948]"}, {"versioned_ensembl_gene_id":"ENSG00000244513.6","gene_symbol":"AC109587.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69013941,"end":69056622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000062282.14","gene_symbol":"DGAT2","gene_name":"diacylglycerol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84649","summary":"This gene encodes one of two enzymes which catalyzes the final reaction in the synthesis of triglycerides in which diacylglycerol is covalently bound to long chain fatty acyl-CoAs. The encoded protein catalyzes this reaction at low concentrations of magnesium chloride while the other enzyme has high activity at high concentrations of magnesium chloride. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":75759512,"end":75801535,"strand":1,"description":"diacylglycerol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16940]"}, {"versioned_ensembl_gene_id":"ENSG00000254814.1","gene_symbol":"AP003031.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75800877,"end":75803415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184922.13","gene_symbol":"FMNL1","gene_name":"formin like 1 [Source:HGNC Symbol;Acc:HGNC:1212]","synonyms":"FMNL,C17orf1B,C17orf1","biotype":"protein_coding","ncbi_id":"752","summary":"This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. An alternative splice variant has been described but its full length sequence has not been determined. [provided by RefSeq, Jul 2008]","start":45221444,"end":45247320,"strand":1,"description":"formin like 1 [Source:HGNC Symbol;Acc:HGNC:1212]"}, {"versioned_ensembl_gene_id":"ENSG00000138375.12","gene_symbol":"SMARCAL1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a like 1 [Source:HGNC Symbol;Acc:HGNC:11102]","synonyms":"HARP,HHARP","biotype":"protein_coding","ncbi_id":"50485","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008]","start":216412414,"end":216483053,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a like 1 [Source:HGNC Symbol;Acc:HGNC:11102]"}, {"versioned_ensembl_gene_id":"ENSG00000256294.7","gene_symbol":"ZNF225","gene_name":"zinc finger protein 225 [Source:HGNC Symbol;Acc:HGNC:13018]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7768","summary":null,"start":44112181,"end":44134816,"strand":1,"description":"zinc finger protein 225 [Source:HGNC Symbol;Acc:HGNC:13018]"}, {"versioned_ensembl_gene_id":"ENSG00000087495.16","gene_symbol":"PHACTR3","gene_name":"phosphatase and actin regulator 3 [Source:HGNC Symbol;Acc:HGNC:15833]","synonyms":"PPP1R123,C20orf101","biotype":"protein_coding","ncbi_id":"116154","summary":"This gene encodes a member of the phosphatase and actin regulator protein family. The encoded protein is associated with the nuclear scaffold in proliferating cells, and binds to actin and the catalytic subunit of protein phosphatase-1, suggesting that it functions as a regulatory subunit of protein phosphatase-1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":59577509,"end":59847711,"strand":1,"description":"phosphatase and actin regulator 3 [Source:HGNC Symbol;Acc:HGNC:15833]"}, {"versioned_ensembl_gene_id":"ENSG00000100916.13","gene_symbol":"BRMS1L","gene_name":"breast cancer metastasis-suppressor 1 like [Source:HGNC Symbol;Acc:HGNC:20512]","synonyms":"MGC11296,FLJ39177,BRMS1","biotype":"protein_coding","ncbi_id":"84312","summary":"The protein encoded by this gene shows sequence similarity to the human breast carcinoma metastasis suppressor (BRMS1) protein and the mammalian Sds3 (suppressor of defective silencing 3) proteins. This protein is a component of the mSin3a family of histone deacetylase complexes (HDAC). [provided by RefSeq, Jul 2008]","start":35826318,"end":35932325,"strand":1,"description":"breast cancer metastasis-suppressor 1 like [Source:HGNC Symbol;Acc:HGNC:20512]"}, {"versioned_ensembl_gene_id":"ENSG00000258938.1","gene_symbol":"AL162311.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35819224,"end":35826765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233998.1","gene_symbol":"SETP5","gene_name":"SET pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130014","summary":null,"start":137640986,"end":137641547,"strand":-1,"description":"SET pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42924]"}, {"versioned_ensembl_gene_id":"ENSG00000257307.1","gene_symbol":"AL162311.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35881001,"end":35881709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232793.2","gene_symbol":"DNAJC19P8","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45071]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861455","summary":null,"start":245282831,"end":245283089,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45071]"}, {"versioned_ensembl_gene_id":"ENSG00000257826.1","gene_symbol":"AL133304.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36061026,"end":36067190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275059.1","gene_symbol":"GU182343.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54783578,"end":54795926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203993.4","gene_symbol":"ARRDC1-AS1","gene_name":"ARRDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23395]","synonyms":"C9orf37","biotype":"antisense_RNA","ncbi_id":"85026","summary":"This transcribed locus is thought to be non-coding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":137615332,"end":137618906,"strand":-1,"description":"ARRDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23395]"}, {"versioned_ensembl_gene_id":"ENSG00000257720.1","gene_symbol":"ILF2P2","gene_name":"interleukin enhancer binding factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644616","summary":null,"start":36054197,"end":36055313,"strand":-1,"description":"interleukin enhancer binding factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44696]"}, {"versioned_ensembl_gene_id":"ENSG00000236731.1","gene_symbol":"AL135929.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157629939,"end":157630728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278428.1","gene_symbol":"AC022709.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":59893856,"end":59893942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197857.13","gene_symbol":"ZNF44","gene_name":"zinc finger protein 44 [Source:HGNC Symbol;Acc:HGNC:13110]","synonyms":"ZNF58,ZNF55,ZNF504,KOX7","biotype":"protein_coding","ncbi_id":"51710","summary":null,"start":12224686,"end":12294887,"strand":-1,"description":"zinc finger protein 44 [Source:HGNC Symbol;Acc:HGNC:13110]"}, {"versioned_ensembl_gene_id":"ENSG00000253723.1","gene_symbol":"AC107934.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59821124,"end":59821433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253413.1","gene_symbol":"AC107934.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59760047,"end":59760263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184716.13","gene_symbol":"SERINC4","gene_name":"serine incorporator 4 [Source:HGNC Symbol;Acc:HGNC:32237]","synonyms":"FLJ40363","biotype":"protein_coding","ncbi_id":"619189","summary":null,"start":43794162,"end":43800221,"strand":-1,"description":"serine incorporator 4 [Source:HGNC Symbol;Acc:HGNC:32237]"}, {"versioned_ensembl_gene_id":"ENSG00000149596.6","gene_symbol":"JPH2","gene_name":"junctophilin 2 [Source:HGNC Symbol;Acc:HGNC:14202]","synonyms":"JP-2","biotype":"protein_coding","ncbi_id":"57158","summary":"Junctional complexes between the plasma membrane and endoplasmic/sarcoplasmic reticulum are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. The protein encoded by this gene is a component of junctional complexes and is composed of a C-terminal hydrophobic segment spanning the endoplasmic/sarcoplasmic reticulum membrane and a remaining cytoplasmic domain that shows specific affinity for the plasma membrane. This gene is a member of the junctophilin gene family. Alternative splicing has been observed at this locus and two variants encoding distinct isoforms are described. [provided by RefSeq, Jul 2008]","start":44111695,"end":44187578,"strand":-1,"description":"junctophilin 2 [Source:HGNC Symbol;Acc:HGNC:14202]"}, {"versioned_ensembl_gene_id":"ENSG00000249184.1","gene_symbol":"AC107074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151799500,"end":151801348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249708.1","gene_symbol":"AC112242.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151887543,"end":151891263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181852.17","gene_symbol":"RNF41","gene_name":"ring finger protein 41 [Source:HGNC Symbol;Acc:HGNC:18401]","synonyms":"SBBI03,NRDP1","biotype":"protein_coding","ncbi_id":"10193","summary":"This gene encodes an E3 ubiquitin ligase. The encoded protein plays a role in type 1 cytokine receptor signaling by controlling the balance between JAK2-associated cytokine receptor degradation and ectodomain shedding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011]","start":56202175,"end":56221933,"strand":-1,"description":"ring finger protein 41 [Source:HGNC Symbol;Acc:HGNC:18401]"}, {"versioned_ensembl_gene_id":"ENSG00000196782.12","gene_symbol":"MAML3","gene_name":"mastermind like transcriptional coactivator 3 [Source:HGNC Symbol;Acc:HGNC:16272]","synonyms":"TNRC3,MAM2,KIAA1816,GDN,CAGH3","biotype":"protein_coding","ncbi_id":"55534","summary":null,"start":139716753,"end":140154184,"strand":-1,"description":"mastermind like transcriptional coactivator 3 [Source:HGNC Symbol;Acc:HGNC:16272]"}, {"versioned_ensembl_gene_id":"ENSG00000178458.5","gene_symbol":"H3F3AP6","gene_name":"H3 histone, family 3A, pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42982]","synonyms":"p21","biotype":"processed_pseudogene","ncbi_id":"644914","summary":null,"start":139698144,"end":139698554,"strand":-1,"description":"H3 histone, family 3A, pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42982]"}, {"versioned_ensembl_gene_id":"ENSG00000256299.1","gene_symbol":"AC073912.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130810821,"end":130812622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165682.14","gene_symbol":"CLEC1B","gene_name":"C-type lectin domain family 1 member B [Source:HGNC Symbol;Acc:HGNC:24356]","synonyms":"CLEC2","biotype":"protein_coding","ncbi_id":"51266","summary":"Natural killer (NK) cells express multiple calcium-dependent (C-type) lectin-like receptors, such as CD94 (KLRD1; MIM 602894) and NKG2D (KLRC4; MIM 602893), that interact with major histocompatibility complex class I molecules and either inhibit or activate cytotoxicity and cytokine secretion. CLEC2 is a C-type lectin-like receptor expressed in myeloid cells and NK cells (Colonna et al., 2000 [PubMed 10671229]).[supplied by OMIM, Jan 2011]","start":9985642,"end":10013424,"strand":-1,"description":"C-type lectin domain family 1 member B [Source:HGNC Symbol;Acc:HGNC:24356]"}, {"versioned_ensembl_gene_id":"ENSG00000150433.9","gene_symbol":"TMEM218","gene_name":"transmembrane protein 218 [Source:HGNC Symbol;Acc:HGNC:27344]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219854","summary":null,"start":125096545,"end":125111763,"strand":-1,"description":"transmembrane protein 218 [Source:HGNC Symbol;Acc:HGNC:27344]"}, {"versioned_ensembl_gene_id":"ENSG00000183161.4","gene_symbol":"FANCF","gene_name":"Fanconi anemia complementation group F [Source:HGNC Symbol;Acc:HGNC:3587]","synonyms":"FAF","biotype":"protein_coding","ncbi_id":"2188","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group F. [provided by RefSeq, Jul 2008]","start":22622519,"end":22626787,"strand":-1,"description":"Fanconi anemia complementation group F [Source:HGNC Symbol;Acc:HGNC:3587]"}, {"versioned_ensembl_gene_id":"ENSG00000258752.1","gene_symbol":"AL357093.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89350285,"end":89364699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223396.3","gene_symbol":"RPS10P7","gene_name":"ribosomal protein S10 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36423]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"376693","summary":null,"start":201518703,"end":201530474,"strand":1,"description":"ribosomal protein S10 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36423]"}, {"versioned_ensembl_gene_id":"ENSG00000211935.3","gene_symbol":"IGHV1-3","gene_name":"immunoglobulin heavy variable 1-3 [Source:HGNC Symbol;Acc:HGNC:5552]","synonyms":"VI-3B","biotype":"IG_V_gene","ncbi_id":"28473","summary":null,"start":106005095,"end":106005574,"strand":-1,"description":"immunoglobulin heavy variable 1-3 [Source:HGNC Symbol;Acc:HGNC:5552]"}, {"versioned_ensembl_gene_id":"ENSG00000235740.1","gene_symbol":"PHACTR2-AS1","gene_name":"PHACTR2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40943]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285740","summary":null,"start":143554325,"end":143562031,"strand":-1,"description":"PHACTR2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40943]"}, {"versioned_ensembl_gene_id":"ENSG00000254279.1","gene_symbol":"IGHVII-1-1","gene_name":"immunoglobulin heavy variable (II)-1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5670]","synonyms":"IGHV(II)-1-1","biotype":"IG_V_pseudogene","ncbi_id":"28377","summary":null,"start":105945210,"end":105945389,"strand":-1,"description":"immunoglobulin heavy variable (II)-1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5670]"}, {"versioned_ensembl_gene_id":"ENSG00000165643.10","gene_symbol":"SOHLH1","gene_name":"spermatogenesis and oogenesis specific basic helix-loop-helix 1 [Source:HGNC Symbol;Acc:HGNC:27845]","synonyms":"SPATA27,NOHLH,C9orf157,bHLHe80,bA100C15.3,TEB2","biotype":"protein_coding","ncbi_id":"402381","summary":"This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonobstructive azoospermia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":135693407,"end":135699528,"strand":-1,"description":"spermatogenesis and oogenesis specific basic helix-loop-helix 1 [Source:HGNC Symbol;Acc:HGNC:27845]"}, {"versioned_ensembl_gene_id":"ENSG00000233216.1","gene_symbol":"AL357373.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58228682,"end":58229003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231560.1","gene_symbol":"CLEC12A-AS1","gene_name":"CLEC12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53407]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400002","summary":null,"start":9948137,"end":9953336,"strand":-1,"description":"CLEC12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53407]"}, {"versioned_ensembl_gene_id":"ENSG00000262823.1","gene_symbol":"AC127521.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4481966,"end":4486353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203808.10","gene_symbol":"BVES-AS1","gene_name":"BVES antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21223]","synonyms":"C6orf112,bA99L11.2","biotype":"antisense_RNA","ncbi_id":"154442","summary":null,"start":105136308,"end":105169945,"strand":1,"description":"BVES antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:21223]"}, {"versioned_ensembl_gene_id":"ENSG00000250731.1","gene_symbol":"TPM3P6","gene_name":"tropomyosin 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39169]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653758","summary":null,"start":53479350,"end":53480091,"strand":1,"description":"tropomyosin 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39169]"}, {"versioned_ensembl_gene_id":"ENSG00000178645.12","gene_symbol":"C10orf53","gene_name":"chromosome 10 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:27421]","synonyms":"Em:AC069546.1","biotype":"protein_coding","ncbi_id":"282966","summary":null,"start":49679651,"end":49710261,"strand":1,"description":"chromosome 10 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:27421]"}, {"versioned_ensembl_gene_id":"ENSG00000275385.1","gene_symbol":"CCL18","gene_name":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]","synonyms":"CKb7,SCYA18,AMAC-1,PARC,MIP-4,DCCK1,DC-CK1","biotype":"protein_coding","ncbi_id":"6362","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for naive T cells, CD4+ and CD8+ T cells and nonactivated lymphocytes, but not for monocytes or granulocytes. This chemokine attracts naive T lymphocytes toward dendritic cells and activated macrophages in lymph nodes. It may play a role in both humoral and cell-mediated immunity responses. [provided by RefSeq, Sep 2014]","start":36064280,"end":36072032,"strand":1,"description":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]"}, {"versioned_ensembl_gene_id":"ENSG00000211917.1","gene_symbol":"IGHD3-16","gene_name":"immunoglobulin heavy diversity 3-16 [Source:HGNC Symbol;Acc:HGNC:5496]","synonyms":"IGHD316","biotype":"IG_D_gene","ncbi_id":"28498","summary":null,"start":105895634,"end":105895670,"strand":-1,"description":"immunoglobulin heavy diversity 3-16 [Source:HGNC Symbol;Acc:HGNC:5496]"}, {"versioned_ensembl_gene_id":"ENSG00000254540.1","gene_symbol":"AC040936.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22361213,"end":22362294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173801.16","gene_symbol":"JUP","gene_name":"junction plakoglobin [Source:HGNC Symbol;Acc:HGNC:6207]","synonyms":"PKGB,PDGB,DPIII,DP3,CTNNG","biotype":"protein_coding","ncbi_id":"3728","summary":"This gene encodes a major cytoplasmic protein which is the only known constituent common to submembranous plaques of both desmosomes and intermediate junctions. This protein forms distinct complexes with cadherins and desmosomal cadherins and is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat. Mutation in this gene has been associated with Naxos disease. Alternative splicing occurs in this gene; however, not all transcripts have been fully described. [provided by RefSeq, Jul 2008]","start":41754604,"end":41786931,"strand":-1,"description":"junction plakoglobin [Source:HGNC Symbol;Acc:HGNC:6207]"}, {"versioned_ensembl_gene_id":"ENSG00000250251.6","gene_symbol":"PKD1P6","gene_name":"polycystin 1, transient receptor potential channel interacting pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30070]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"353511","summary":null,"start":15125242,"end":15154564,"strand":-1,"description":"polycystin 1, transient receptor potential channel interacting pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30070]"}, {"versioned_ensembl_gene_id":"ENSG00000236313.1","gene_symbol":"VN1R53P","gene_name":"vomeronasal 1 receptor 53 pseudogene [Source:HGNC Symbol;Acc:HGNC:37373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312806","summary":null,"start":37348616,"end":37349572,"strand":1,"description":"vomeronasal 1 receptor 53 pseudogene [Source:HGNC Symbol;Acc:HGNC:37373]"}, {"versioned_ensembl_gene_id":"ENSG00000227196.1","gene_symbol":"IGHD4-23","gene_name":"immunoglobulin heavy diversity 4-23 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5504]","synonyms":"IGHD423","biotype":"IG_D_gene","ncbi_id":"28493","summary":null,"start":105884870,"end":105884888,"strand":-1,"description":"immunoglobulin heavy diversity 4-23 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5504]"}, {"versioned_ensembl_gene_id":"ENSG00000249438.2","gene_symbol":"KRT18P45","gene_name":"keratin 18 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:33415]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391803","summary":null,"start":80288449,"end":80289781,"strand":1,"description":"keratin 18 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:33415]"}, {"versioned_ensembl_gene_id":"ENSG00000235991.4","gene_symbol":"BX293995.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155137111,"end":155156503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257591.5","gene_symbol":"ZNF625","gene_name":"zinc finger protein 625 [Source:HGNC Symbol;Acc:HGNC:30571]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90589","summary":null,"start":12142090,"end":12156729,"strand":-1,"description":"zinc finger protein 625 [Source:HGNC Symbol;Acc:HGNC:30571]"}, {"versioned_ensembl_gene_id":"ENSG00000172375.12","gene_symbol":"C2CD2L","gene_name":"C2CD2 like [Source:HGNC Symbol;Acc:HGNC:29000]","synonyms":"TMEM24,KIAA0285","biotype":"protein_coding","ncbi_id":"9854","summary":null,"start":119102198,"end":119118544,"strand":1,"description":"C2CD2 like [Source:HGNC Symbol;Acc:HGNC:29000]"}, {"versioned_ensembl_gene_id":"ENSG00000270655.1","gene_symbol":"AL031320.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143386581,"end":143387409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211890.4","gene_symbol":"IGHA2","gene_name":"immunoglobulin heavy constant alpha 2 (A2m marker) [Source:HGNC Symbol;Acc:HGNC:5479]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3494","summary":null,"start":105583731,"end":105588395,"strand":-1,"description":"immunoglobulin heavy constant alpha 2 (A2m marker) [Source:HGNC Symbol;Acc:HGNC:5479]"}, {"versioned_ensembl_gene_id":"ENSG00000167355.7","gene_symbol":"AC087380.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":5304976,"end":5505652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283663.1","gene_symbol":"AC008687.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49055793,"end":49065076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178913.7","gene_symbol":"TAF7","gene_name":"TATA-box binding protein associated factor 7 [Source:HGNC Symbol;Acc:HGNC:11541]","synonyms":"TAFII55,TAF2F","biotype":"protein_coding","ncbi_id":"6879","summary":"The intronless gene for this transcription coactivator is located between the protocadherin beta and gamma gene clusters on chromosome 5. The protein encoded by this gene is a component of the TFIID protein complex, a complex which binds to the TATA box in class II promoters and recruits RNA polymerase II and other factors. This particular subunit interacts with the largest TFIID subunit, as well as multiple transcription activators. The protein is required for transcription by promoters targeted by RNA polymerase II. [provided by RefSeq, Jul 2008]","start":141260225,"end":141320821,"strand":-1,"description":"TATA-box binding protein associated factor 7 [Source:HGNC Symbol;Acc:HGNC:11541]"}, {"versioned_ensembl_gene_id":"ENSG00000211593.2","gene_symbol":"IGKJ5","gene_name":"immunoglobulin kappa joining 5 [Source:HGNC Symbol;Acc:HGNC:5723]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28946","summary":null,"start":88860568,"end":88860605,"strand":-1,"description":"immunoglobulin kappa joining 5 [Source:HGNC Symbol;Acc:HGNC:5723]"}, {"versioned_ensembl_gene_id":"ENSG00000211594.2","gene_symbol":"IGKJ4","gene_name":"immunoglobulin kappa joining 4 [Source:HGNC Symbol;Acc:HGNC:5722]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28947","summary":null,"start":88860886,"end":88860922,"strand":-1,"description":"immunoglobulin kappa joining 4 [Source:HGNC Symbol;Acc:HGNC:5722]"}, {"versioned_ensembl_gene_id":"ENSG00000229847.8","gene_symbol":"EMX2OS","gene_name":"EMX2 opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:18511]","synonyms":"NCRNA00045,EMX2-AS1","biotype":"antisense_RNA","ncbi_id":"196047","summary":null,"start":117473215,"end":117545068,"strand":-1,"description":"EMX2 opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:18511]"}, {"versioned_ensembl_gene_id":"ENSG00000234093.3","gene_symbol":"RPS15AP11","gene_name":"ribosomal protein S15a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36707]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644790","summary":null,"start":44780331,"end":44780715,"strand":-1,"description":"ribosomal protein S15a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36707]"}, {"versioned_ensembl_gene_id":"ENSG00000081818.3","gene_symbol":"PCDHB4","gene_name":"protocadherin beta 4 [Source:HGNC Symbol;Acc:HGNC:8689]","synonyms":"PCDH-BETA4","biotype":"protein_coding","ncbi_id":"56131","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141121799,"end":141125623,"strand":1,"description":"protocadherin beta 4 [Source:HGNC Symbol;Acc:HGNC:8689]"}, {"versioned_ensembl_gene_id":"ENSG00000140395.8","gene_symbol":"WDR61","gene_name":"WD repeat domain 61 [Source:HGNC Symbol;Acc:HGNC:30300]","synonyms":"REC14","biotype":"protein_coding","ncbi_id":"80349","summary":"WDR61 is a subunit of the human PAF and SKI complexes, which function in transcriptional regulation and are involved in events downstream of RNA synthesis, such as RNA surveillance (Zhu et al., 2005 [PubMed 16024656]).[supplied by OMIM, Mar 2008]","start":78277835,"end":78299794,"strand":-1,"description":"WD repeat domain 61 [Source:HGNC Symbol;Acc:HGNC:30300]"}, {"versioned_ensembl_gene_id":"ENSG00000258740.1","gene_symbol":"AL691403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75238616,"end":75269283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226276.1","gene_symbol":"AC093382.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215939308,"end":215941719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230077.1","gene_symbol":"MTAPP2","gene_name":"methylthioadenosine phosphorylase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42443]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420621","summary":null,"start":189969030,"end":189969861,"strand":-1,"description":"methylthioadenosine phosphorylase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42443]"}, {"versioned_ensembl_gene_id":"ENSG00000259339.2","gene_symbol":"TGIF1P1","gene_name":"TGFB induced factor homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30730]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126052","summary":null,"start":46136746,"end":46137547,"strand":-1,"description":"TGFB induced factor homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30730]"}, {"versioned_ensembl_gene_id":"ENSG00000165953.9","gene_symbol":"SERPINA12","gene_name":"serpin family A member 12 [Source:HGNC Symbol;Acc:HGNC:18359]","synonyms":"Vaspin,OL-64","biotype":"protein_coding","ncbi_id":"145264","summary":null,"start":94487274,"end":94517844,"strand":-1,"description":"serpin family A member 12 [Source:HGNC Symbol;Acc:HGNC:18359]"}, {"versioned_ensembl_gene_id":"ENSG00000204866.8","gene_symbol":"IGFL2","gene_name":"IGF like family member 2 [Source:HGNC Symbol;Acc:HGNC:32929]","synonyms":"UNQ645","biotype":"protein_coding","ncbi_id":"147920","summary":"IGFL2 belongs to the insulin-like growth factor (IGF; see MIM 147440) family of signaling molecules that play critical roles in cellular energy metabolism and in growth and development, especially prenatal growth (Emtage et al., 2006 [PubMed 16890402]).[supplied by OMIM, Mar 2008]","start":46143106,"end":46161299,"strand":1,"description":"IGF like family member 2 [Source:HGNC Symbol;Acc:HGNC:32929]"}, {"versioned_ensembl_gene_id":"ENSG00000251614.1","gene_symbol":"HSPA8P19","gene_name":"heat shock protein family A (Hsp70) member pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:44935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420049","summary":null,"start":132645831,"end":132650383,"strand":1,"description":"heat shock protein family A (Hsp70) member pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:44935]"}, {"versioned_ensembl_gene_id":"ENSG00000197768.10","gene_symbol":"STPG3","gene_name":"sperm-tail PG-rich repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:37285]","synonyms":"FLJ40246,C9orf173","biotype":"protein_coding","ncbi_id":"441476","summary":null,"start":137251261,"end":137253483,"strand":1,"description":"sperm-tail PG-rich repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:37285]"}, {"versioned_ensembl_gene_id":"ENSG00000281963.1","gene_symbol":"TRBV25-1","gene_name":"T-cell receptor beta variable 25-1 [Source:HGNC Symbol;Acc:HGNC:12205]","synonyms":"TRBV251,TCRBV25S1,TCRBV11S1A1T","biotype":"TR_V_gene","ncbi_id":"28562","summary":null,"start":142711413,"end":142711917,"strand":1,"description":"T-cell receptor beta variable 25-1 [Source:HGNC Symbol;Acc:HGNC:12205]"}, {"versioned_ensembl_gene_id":"ENSG00000095319.14","gene_symbol":"NUP188","gene_name":"nucleoporin 188 [Source:HGNC Symbol;Acc:HGNC:17859]","synonyms":"KIAA0169","biotype":"protein_coding","ncbi_id":"23511","summary":"The nuclear pore complex (NPC) is found on the nuclear envelope and forms a gateway that regulates the flow of proteins and RNAs between the cytoplasm and nucleoplasm. The NPC is comprised of approximately 30 distinct proteins collectively known as nucleoporins. Nucleoporins are pore-complex-specific glycoproteins which often have cytoplasmically oriented O-linked N-acetylglucosamine residues and numerous repeats of the pentapeptide sequence XFXFG. However, the nucleoporin protein encoded by this gene does not contain the typical FG repeat sequences found in most vertebrate nucleoporins. This nucleoporin is thought to form part of the scaffold for the central channel of the nuclear pore. [provided by RefSeq, Jan 2013]","start":128947699,"end":129007096,"strand":1,"description":"nucleoporin 188 [Source:HGNC Symbol;Acc:HGNC:17859]"}, {"versioned_ensembl_gene_id":"ENSG00000223606.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29788252,"end":29795033,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000225002.2","gene_symbol":"AL732323.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106061354,"end":106064825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228143.2","gene_symbol":"AL512649.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106722350,"end":106722930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234810.2","gene_symbol":"AL603840.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55581037,"end":55868248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232198.2","gene_symbol":"MTCO2P34","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:52316]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729142","summary":null,"start":55372710,"end":55373316,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:52316]"}, {"versioned_ensembl_gene_id":"ENSG00000231900.3","gene_symbol":"GOT2P1","gene_name":"glutamic-oxaloacetic transaminase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4434]","synonyms":"GOT2L1","biotype":"processed_pseudogene","ncbi_id":"645538","summary":null,"start":55367466,"end":55368774,"strand":1,"description":"glutamic-oxaloacetic transaminase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4434]"}, {"versioned_ensembl_gene_id":"ENSG00000234567.1","gene_symbol":"AL024497.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133452857,"end":133456605,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243831.1","gene_symbol":"AL109933.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160666228,"end":160676523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223542.1","gene_symbol":"AL024497.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133435077,"end":133439464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279343.1","gene_symbol":"AC127071.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130350996,"end":130351707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236795.1","gene_symbol":"AC006004.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147080934,"end":147097609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245498.6","gene_symbol":"AP000866.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124800450,"end":124834487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273514.1","gene_symbol":"FOXD4L6","gene_name":"forkhead box D4 like 6 [Source:HGNC Symbol;Acc:HGNC:31986]","synonyms":"OTTHUMG00000066822","biotype":"protein_coding","ncbi_id":"653404","summary":null,"start":41126430,"end":41128463,"strand":-1,"description":"forkhead box D4 like 6 [Source:HGNC Symbol;Acc:HGNC:31986]"}, {"versioned_ensembl_gene_id":"ENSG00000235201.1","gene_symbol":"AL589703.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118740563,"end":118745312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268601.1","gene_symbol":"AC115522.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43794309,"end":43795658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234660.1","gene_symbol":"LINC00440","gene_name":"long intergenic non-protein coding RNA 440 [Source:HGNC Symbol;Acc:HGNC:42777]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874172","summary":null,"start":89273203,"end":89280240,"strand":1,"description":"long intergenic non-protein coding RNA 440 [Source:HGNC Symbol;Acc:HGNC:42777]"}, {"versioned_ensembl_gene_id":"ENSG00000171940.13","gene_symbol":"ZNF217","gene_name":"zinc finger protein 217 [Source:HGNC Symbol;Acc:HGNC:13009]","synonyms":"ZABC1","biotype":"protein_coding","ncbi_id":"7764","summary":null,"start":53567065,"end":53609907,"strand":-1,"description":"zinc finger protein 217 [Source:HGNC Symbol;Acc:HGNC:13009]"}, {"versioned_ensembl_gene_id":"ENSG00000242568.1","gene_symbol":"AC121764.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55335462,"end":55350915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240058.3","gene_symbol":"AC093267.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122675795,"end":122676755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242775.1","gene_symbol":"AC121764.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55360443,"end":55361829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118990.5","gene_symbol":"GLRXP3","gene_name":"glutaredoxin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34049]","synonyms":"GLRXL","biotype":"processed_pseudogene","ncbi_id":"100132510","summary":null,"start":161751448,"end":161751768,"strand":-1,"description":"glutaredoxin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34049]"}, {"versioned_ensembl_gene_id":"ENSG00000251538.5","gene_symbol":"LINC02201","gene_name":"long intergenic non-protein coding RNA 2201 [Source:HGNC Symbol;Acc:HGNC:53067]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927379","summary":null,"start":122628952,"end":122730685,"strand":-1,"description":"long intergenic non-protein coding RNA 2201 [Source:HGNC Symbol;Acc:HGNC:53067]"}, {"versioned_ensembl_gene_id":"ENSG00000083782.7","gene_symbol":"EPYC","gene_name":"epiphycan [Source:HGNC Symbol;Acc:HGNC:3053]","synonyms":"SLRR3B,Pg-Lb,DSPG3","biotype":"protein_coding","ncbi_id":"1833","summary":"Dermatan sulfate proteoglycan 3 is a member of the small leucine-rich repeat proteoglycan family. This gene is composed of seven exons. It regulates fibrillogenesis by interacting with collagen fibrils and other extracellular matrix proteins. [provided by RefSeq, Jul 2008]","start":90963679,"end":91005026,"strand":-1,"description":"epiphycan [Source:HGNC Symbol;Acc:HGNC:3053]"}, {"versioned_ensembl_gene_id":"ENSG00000225530.1","gene_symbol":"SP3P","gene_name":"Sp3 transcription factor pseudogene [Source:HGNC Symbol;Acc:HGNC:35430]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"160824","summary":null,"start":89361160,"end":89363224,"strand":-1,"description":"Sp3 transcription factor pseudogene [Source:HGNC Symbol;Acc:HGNC:35430]"}, {"versioned_ensembl_gene_id":"ENSG00000226037.1","gene_symbol":"LINC01040","gene_name":"long intergenic non-protein coding RNA 1040 [Source:HGNC Symbol;Acc:HGNC:49028]","synonyms":"TCONS_00021682","biotype":"lincRNA","ncbi_id":"105370308","summary":null,"start":89477608,"end":89500509,"strand":-1,"description":"long intergenic non-protein coding RNA 1040 [Source:HGNC Symbol;Acc:HGNC:49028]"}, {"versioned_ensembl_gene_id":"ENSG00000236176.2","gene_symbol":"LINC00353","gene_name":"long intergenic non-protein coding RNA 353 [Source:HGNC Symbol;Acc:HGNC:42671]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874139","summary":null,"start":89548691,"end":89553804,"strand":-1,"description":"long intergenic non-protein coding RNA 353 [Source:HGNC Symbol;Acc:HGNC:42671]"}, {"versioned_ensembl_gene_id":"ENSG00000125449.6","gene_symbol":"ARMC7","gene_name":"armadillo repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:26168]","synonyms":"FLJ22160","biotype":"protein_coding","ncbi_id":"79637","summary":null,"start":75109952,"end":75130265,"strand":1,"description":"armadillo repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:26168]"}, {"versioned_ensembl_gene_id":"ENSG00000231901.1","gene_symbol":"AL354754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117840322,"end":117897256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271395.1","gene_symbol":"LINC02336","gene_name":"long intergenic non-protein coding RNA 2336 [Source:HGNC Symbol;Acc:HGNC:53256]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370309","summary":null,"start":89551233,"end":89552389,"strand":1,"description":"long intergenic non-protein coding RNA 2336 [Source:HGNC Symbol;Acc:HGNC:53256]"}, {"versioned_ensembl_gene_id":"ENSG00000228512.2","gene_symbol":"AL160272.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117783448,"end":117868071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236848.2","gene_symbol":"RPL23AP95","gene_name":"ribosomal protein L23a pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:51630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480338","summary":null,"start":103152007,"end":103152325,"strand":-1,"description":"ribosomal protein L23a pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:51630]"}, {"versioned_ensembl_gene_id":"ENSG00000279482.1","gene_symbol":"AC007683.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":103161947,"end":103162660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235415.1","gene_symbol":"AC005808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53608354,"end":53634590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234782.3","gene_symbol":"TPT1P9","gene_name":"tumor protein, translationally-controlled 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49299]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389787","summary":null,"start":118082869,"end":118083382,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49299]"}, {"versioned_ensembl_gene_id":"ENSG00000197670.6","gene_symbol":"AL157838.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53552770,"end":53575863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188229.5","gene_symbol":"TUBB4B","gene_name":"tubulin beta 4B class IVb [Source:HGNC Symbol;Acc:HGNC:20771]","synonyms":"TUBB2C,Beta2","biotype":"protein_coding","ncbi_id":"10383","summary":null,"start":137241213,"end":137243707,"strand":1,"description":"tubulin beta 4B class IVb [Source:HGNC Symbol;Acc:HGNC:20771]"}, {"versioned_ensembl_gene_id":"ENSG00000198569.9","gene_symbol":"SLC34A3","gene_name":"solute carrier family 34 member 3 [Source:HGNC Symbol;Acc:HGNC:20305]","synonyms":"NPTIIc,FLJ38680","biotype":"protein_coding","ncbi_id":"142680","summary":"This gene encodes a member of SLC34A transporter family of proteins, and is expressed primarily in the kidney. It is involved in transporting phosphate into cells via sodium cotransport in the renal brush border membrane, and contributes to the maintenance of inorganic phosphate concentration in the kidney. Mutations in this gene are associated with hereditary hypophosphatemic rickets with hypercalciuria. Alternatively spliced transcript variants varying in the 5' UTR have been found for this gene.[provided by RefSeq, Apr 2010]","start":137230757,"end":137236554,"strand":1,"description":"solute carrier family 34 member 3 [Source:HGNC Symbol;Acc:HGNC:20305]"}, {"versioned_ensembl_gene_id":"ENSG00000074071.14","gene_symbol":"MRPS34","gene_name":"mitochondrial ribosomal protein S34 [Source:HGNC Symbol;Acc:HGNC:16618]","synonyms":"MRP-S12,MGC2616","biotype":"protein_coding","ncbi_id":"65993","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":1771890,"end":1773155,"strand":-1,"description":"mitochondrial ribosomal protein S34 [Source:HGNC Symbol;Acc:HGNC:16618]"}, {"versioned_ensembl_gene_id":"ENSG00000125458.6","gene_symbol":"NT5C","gene_name":"5', 3'-nucleotidase, cytosolic [Source:HGNC Symbol;Acc:HGNC:17144]","synonyms":"UMPH2,PN-I,DNT1,DNT-1,cdN","biotype":"protein_coding","ncbi_id":"30833","summary":"This gene encodes a nucleotidase that catalyzes the dephosphorylation of the 5' deoxyribonucleotides (dNTP) and 2'(3')-dNTP and ribonucleotides, but not 5' ribonucleotides. Of the different forms of nucleotidases characterized, this enzyme is unique in its preference for 5'-dNTP. It may be one of the enzymes involved in regulating the size of dNTP pools in cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2011]","start":75130225,"end":75131795,"strand":-1,"description":"5', 3'-nucleotidase, cytosolic [Source:HGNC Symbol;Acc:HGNC:17144]"}, {"versioned_ensembl_gene_id":"ENSG00000254460.1","gene_symbol":"AP002815.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75506937,"end":75508391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159871.14","gene_symbol":"LYPD5","gene_name":"LY6/PLAUR domain containing 5 [Source:HGNC Symbol;Acc:HGNC:26397]","synonyms":"FLJ30469","biotype":"protein_coding","ncbi_id":"284348","summary":null,"start":43795929,"end":43827206,"strand":-1,"description":"LY6/PLAUR domain containing 5 [Source:HGNC Symbol;Acc:HGNC:26397]"}, {"versioned_ensembl_gene_id":"ENSG00000158555.14","gene_symbol":"GDPD5","gene_name":"glycerophosphodiester phosphodiesterase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28804]","synonyms":"PP1665,GDE2","biotype":"protein_coding","ncbi_id":"81544","summary":"Glycerophosphodiester phosphodiesterases (GDPDs; EC 3.1.4.46), such as GDPD5, are involved in glycerol metabolism (Lang et al., 2008 [PubMed 17578682]).[supplied by OMIM, Jan 2010]","start":75434640,"end":75525903,"strand":-1,"description":"glycerophosphodiester phosphodiesterase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28804]"}, {"versioned_ensembl_gene_id":"ENSG00000188163.7","gene_symbol":"FAM166A","gene_name":"family with sequence similarity 166 member A [Source:HGNC Symbol;Acc:HGNC:33818]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401565","summary":null,"start":137243584,"end":137247770,"strand":-1,"description":"family with sequence similarity 166 member A [Source:HGNC Symbol;Acc:HGNC:33818]"}, {"versioned_ensembl_gene_id":"ENSG00000215893.3","gene_symbol":"RPL23AP17","gene_name":"ribosomal protein L23a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271138","summary":null,"start":41098638,"end":41099136,"strand":1,"description":"ribosomal protein L23a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35904]"}, {"versioned_ensembl_gene_id":"ENSG00000234227.1","gene_symbol":"RPL7L1P1","gene_name":"ribosomal protein L7 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129260","summary":null,"start":89833157,"end":89833941,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39455]"}, {"versioned_ensembl_gene_id":"ENSG00000215418.2","gene_symbol":"PEX12P1","gene_name":"peroxisomal biogenesis factor 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39678]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"121727","summary":null,"start":89991831,"end":89992878,"strand":1,"description":"peroxisomal biogenesis factor 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39678]"}, {"versioned_ensembl_gene_id":"ENSG00000154146.12","gene_symbol":"NRGN","gene_name":"neurogranin [Source:HGNC Symbol;Acc:HGNC:8000]","synonyms":"RC3","biotype":"protein_coding","ncbi_id":"4900","summary":"Neurogranin (NRGN) is the human homolog of the neuron-specific rat RC3/neurogranin gene. This gene encodes a postsynaptic protein kinase substrate that binds calmodulin in the absence of calcium. The NRGN gene contains four exons and three introns. The exons 1 and 2 encode the protein and exons 3 and 4 contain untranslated sequences. It is suggested that the NRGN is a direct target for thyroid hormone in human brain, and that control of expression of this gene could underlay many of the consequences of hypothyroidism on mental states during development as well as in adult subjects. [provided by RefSeq, Jul 2008]","start":124739846,"end":124747210,"strand":1,"description":"neurogranin [Source:HGNC Symbol;Acc:HGNC:8000]"}, {"versioned_ensembl_gene_id":"ENSG00000010803.16","gene_symbol":"SCMH1","gene_name":"sex comb on midleg homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:19003]","synonyms":"Scml3","biotype":"protein_coding","ncbi_id":"22955","summary":null,"start":41027200,"end":41242154,"strand":-1,"description":"sex comb on midleg homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:19003]"}, {"versioned_ensembl_gene_id":"ENSG00000236561.9","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTNL11,BTN6","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29657481,"end":29672869,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000255045.1","gene_symbol":"AP000866.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124744634,"end":124746337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244586.1","gene_symbol":"WNT5A-AS1","gene_name":"WNT5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40616]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874008","summary":null,"start":55487699,"end":55488308,"strand":1,"description":"WNT5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40616]"}, {"versioned_ensembl_gene_id":"ENSG00000114251.14","gene_symbol":"WNT5A","gene_name":"Wnt family member 5A [Source:HGNC Symbol;Acc:HGNC:12784]","synonyms":"hWNT5A","biotype":"protein_coding","ncbi_id":"7474","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene encodes a member of the WNT family that signals through both the canonical and non-canonical WNT pathways. This protein is a ligand for the seven transmembrane receptor frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":55465715,"end":55490539,"strand":-1,"description":"Wnt family member 5A [Source:HGNC Symbol;Acc:HGNC:12784]"}, {"versioned_ensembl_gene_id":"ENSG00000134248.13","gene_symbol":"LAMTOR5","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 [Source:HGNC Symbol;Acc:HGNC:17955]","synonyms":"XIP,MGC71071,HBXIP","biotype":"protein_coding","ncbi_id":"10542","summary":"This gene encodes a protein that specifically complexes with the C-terminus of hepatitis B virus X protein (HBx). The function of this protein is to negatively regulate HBx activity and thus to alter the replication life cycle of the virus. [provided by RefSeq, Jul 2008]","start":110401249,"end":110407942,"strand":-1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 [Source:HGNC Symbol;Acc:HGNC:17955]"}, {"versioned_ensembl_gene_id":"ENSG00000171360.3","gene_symbol":"KRT38","gene_name":"keratin 38 [Source:HGNC Symbol;Acc:HGNC:6456]","synonyms":"KRTHA8","biotype":"protein_coding","ncbi_id":"8687","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41436446,"end":41440921,"strand":-1,"description":"keratin 38 [Source:HGNC Symbol;Acc:HGNC:6456]"}, {"versioned_ensembl_gene_id":"ENSG00000225050.1","gene_symbol":"AL355592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118687752,"end":118705960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253403.1","gene_symbol":"AC091944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161687347,"end":161689408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280132.1","gene_symbol":"AC026471.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31470204,"end":31472108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186854.10","gene_symbol":"TRABD2A","gene_name":"TraB domain containing 2A [Source:HGNC Symbol;Acc:HGNC:27013]","synonyms":"TIKI1,C2orf89","biotype":"protein_coding","ncbi_id":"129293","summary":null,"start":84821650,"end":84907008,"strand":-1,"description":"TraB domain containing 2A [Source:HGNC Symbol;Acc:HGNC:27013]"}, {"versioned_ensembl_gene_id":"ENSG00000108417.3","gene_symbol":"KRT37","gene_name":"keratin 37 [Source:HGNC Symbol;Acc:HGNC:6455]","synonyms":"KRTHA7","biotype":"protein_coding","ncbi_id":"8688","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41420753,"end":41424523,"strand":-1,"description":"keratin 37 [Source:HGNC Symbol;Acc:HGNC:6455]"}, {"versioned_ensembl_gene_id":"ENSG00000213400.3","gene_symbol":"RPL12P18","gene_name":"ribosomal protein L12 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36750]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729760","summary":null,"start":84874696,"end":84875020,"strand":1,"description":"ribosomal protein L12 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36750]"}, {"versioned_ensembl_gene_id":"ENSG00000168447.10","gene_symbol":"SCNN1B","gene_name":"sodium channel epithelial 1 beta subunit [Source:HGNC Symbol;Acc:HGNC:10600]","synonyms":"ENaCbeta","biotype":"protein_coding","ncbi_id":"6338","summary":"Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009]","start":23278231,"end":23381299,"strand":1,"description":"sodium channel epithelial 1 beta subunit [Source:HGNC Symbol;Acc:HGNC:10600]"}, {"versioned_ensembl_gene_id":"ENSG00000282730.1","gene_symbol":"TRBV24-1","gene_name":"T-cell receptor beta variable 24-1 [Source:HGNC Symbol;Acc:HGNC:12203]","synonyms":"TRBV241,TCRBV24S1,TCRBV15S1","biotype":"TR_V_gene","ncbi_id":"28563","summary":null,"start":142697038,"end":142697550,"strand":1,"description":"T-cell receptor beta variable 24-1 [Source:HGNC Symbol;Acc:HGNC:12203]"}, {"versioned_ensembl_gene_id":"ENSG00000145863.10","gene_symbol":"GABRA6","gene_name":"gamma-aminobutyric acid type A receptor alpha6 subunit [Source:HGNC Symbol;Acc:HGNC:4080]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2559","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. [provided by RefSeq, Jul 2008]","start":161547063,"end":161702593,"strand":1,"description":"gamma-aminobutyric acid type A receptor alpha6 subunit [Source:HGNC Symbol;Acc:HGNC:4080]"}, {"versioned_ensembl_gene_id":"ENSG00000282771.1","gene_symbol":"AC239612.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142657499,"end":142658198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214929.3","gene_symbol":"SPATA31D1","gene_name":"SPATA31 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:37283]","synonyms":"FLJ46321,FAM75D1","biotype":"protein_coding","ncbi_id":"389763","summary":null,"start":81988772,"end":81995256,"strand":1,"description":"SPATA31 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:37283]"}, {"versioned_ensembl_gene_id":"ENSG00000198961.9","gene_symbol":"PJA2","gene_name":"praja ring finger ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:17481]","synonyms":"RNF131,Neurodap1,KIAA0438","biotype":"protein_coding","ncbi_id":"9867","summary":null,"start":109334709,"end":109409994,"strand":-1,"description":"praja ring finger ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:17481]"}, {"versioned_ensembl_gene_id":"ENSG00000243873.1","gene_symbol":"HMGB1P36","gene_name":"high mobility group box 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419968","summary":null,"start":70753854,"end":70754573,"strand":1,"description":"high mobility group box 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39176]"}, {"versioned_ensembl_gene_id":"ENSG00000237338.1","gene_symbol":"FTCD-AS1","gene_name":"FTCD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40243]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861507","summary":null,"start":46151614,"end":46152647,"strand":1,"description":"FTCD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40243]"}, {"versioned_ensembl_gene_id":"ENSG00000273656.4","gene_symbol":"AC139494.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69755077,"end":69848798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154143.2","gene_symbol":"PANX3","gene_name":"pannexin 3 [Source:HGNC Symbol;Acc:HGNC:20573]","synonyms":"Px3","biotype":"protein_coding","ncbi_id":"116337","summary":"The protein encoded by this gene belongs to the innexin family. Innexin family members are known to be the structural components of gap junctions. [provided by RefSeq, Jul 2008]","start":124611490,"end":124620356,"strand":1,"description":"pannexin 3 [Source:HGNC Symbol;Acc:HGNC:20573]"}, {"versioned_ensembl_gene_id":"ENSG00000267002.2","gene_symbol":"AC060780.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43148368,"end":43171037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119401.10","gene_symbol":"TRIM32","gene_name":"tripartite motif containing 32 [Source:HGNC Symbol;Acc:HGNC:16380]","synonyms":"TATIP,LGMD2H,HT2A,BBS11","biotype":"protein_coding","ncbi_id":"22954","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. The protein has also been localized to the nucleus, where it interacts with the activation domain of the HIV-1 Tat protein. The Tat protein activates transcription of HIV-1 genes. [provided by RefSeq, Jul 2008]","start":116687302,"end":116701300,"strand":1,"description":"tripartite motif containing 32 [Source:HGNC Symbol;Acc:HGNC:16380]"}, {"versioned_ensembl_gene_id":"ENSG00000163810.11","gene_symbol":"TGM4","gene_name":"transglutaminase 4 [Source:HGNC Symbol;Acc:HGNC:11780]","synonyms":"TGP","biotype":"protein_coding","ncbi_id":"7047","summary":null,"start":44874608,"end":44914990,"strand":1,"description":"transglutaminase 4 [Source:HGNC Symbol;Acc:HGNC:11780]"}, {"versioned_ensembl_gene_id":"ENSG00000227895.5","gene_symbol":"ISX-AS1","gene_name":"ISX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41188]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926957","summary":null,"start":34997719,"end":35002862,"strand":-1,"description":"ISX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41188]"}, {"versioned_ensembl_gene_id":"ENSG00000275137.1","gene_symbol":"AC008746.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54438579,"end":54442625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233702.1","gene_symbol":"AC107083.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62507545,"end":62507823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249510.1","gene_symbol":"AP003478.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94201913,"end":94203052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160606.10","gene_symbol":"TLCD1","gene_name":"TLC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116238","summary":null,"start":28724348,"end":28727935,"strand":-1,"description":"TLC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25177]"}, {"versioned_ensembl_gene_id":"ENSG00000182919.14","gene_symbol":"C11orf54","gene_name":"chromosome 11 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:30204]","synonyms":"PTD012","biotype":"protein_coding","ncbi_id":"28970","summary":null,"start":93741591,"end":93764749,"strand":1,"description":"chromosome 11 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:30204]"}, {"versioned_ensembl_gene_id":"ENSG00000248098.11","gene_symbol":"BCKDHA","gene_name":"branched chain keto acid dehydrogenase E1, alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:986]","synonyms":"OVD1A,MSU","biotype":"protein_coding","ncbi_id":"593","summary":"The branched-chain alpha-keto acid (BCAA) dehydrogenase (BCKD) complex is an innter mitochondrial enzyme complex that catalyzes the second major step in the catabolism of the branched-chain amino acids leucine, isoleucine, and valine. The BCKD complex consists of three catalytic components: a heterotetrameric (alpha2-beta2) branched-chain alpha-keto acid decarboxylase (E1), a dihydrolipoyl transacylase (E2), and a dihydrolipoamide dehydrogenase (E3). This gene encodes the alpha subunit of the decarboxylase (E1) component. Mutations in this gene result in maple syrup urine disease, type IA. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":41397460,"end":41425005,"strand":1,"description":"branched chain keto acid dehydrogenase E1, alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:986]"}, {"versioned_ensembl_gene_id":"ENSG00000106682.14","gene_symbol":"EIF4H","gene_name":"eukaryotic translation initiation factor 4H [Source:HGNC Symbol;Acc:HGNC:12741]","synonyms":"WSCR1,WBSCR1,KIAA0038","biotype":"protein_coding","ncbi_id":"7458","summary":"This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":74174245,"end":74197101,"strand":1,"description":"eukaryotic translation initiation factor 4H [Source:HGNC Symbol;Acc:HGNC:12741]"}, {"versioned_ensembl_gene_id":"ENSG00000152455.15","gene_symbol":"SUV39H2","gene_name":"suppressor of variegation 3-9 homolog 2 [Source:HGNC Symbol;Acc:HGNC:17287]","synonyms":"KMT1B,FLJ23414","biotype":"protein_coding","ncbi_id":"79723","summary":null,"start":14878820,"end":14904315,"strand":1,"description":"suppressor of variegation 3-9 homolog 2 [Source:HGNC Symbol;Acc:HGNC:17287]"}, {"versioned_ensembl_gene_id":"ENSG00000267107.6","gene_symbol":"PCAT19","gene_name":"prostate cancer associated transcript 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49593]","synonyms":"LOC100505495,LINC01190","biotype":"lincRNA","ncbi_id":"100505495","summary":null,"start":41454169,"end":41500649,"strand":-1,"description":"prostate cancer associated transcript 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49593]"}, {"versioned_ensembl_gene_id":"ENSG00000274610.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"protein_coding","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54771258,"end":54784662,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000238053.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29708062,"end":29708484,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000014257.15","gene_symbol":"ACPP","gene_name":"acid phosphatase, prostate [Source:HGNC Symbol;Acc:HGNC:125]","synonyms":"PAP,ACP3,ACP-3","biotype":"protein_coding","ncbi_id":"55","summary":"This gene encodes an enzyme that catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate. It is synthesized under androgen regulation and is secreted by the epithelial cells of the prostate gland. An alternatively spliced transcript variant encoding a longer isoform has been found for this gene. This isoform contains a transmembrane domain and is localized in the plasma membrane-endosomal-lysosomal pathway. [provided by RefSeq, Sep 2008]","start":132317367,"end":132368298,"strand":1,"description":"acid phosphatase, prostate [Source:HGNC Symbol;Acc:HGNC:125]"}, {"versioned_ensembl_gene_id":"ENSG00000225380.4","gene_symbol":"IGKV1OR9-2","gene_name":"immunoglobulin kappa variable 1/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49466]","synonyms":"IGKV1/OR9-2","biotype":"IG_V_pseudogene","ncbi_id":"106480274","summary":null,"start":40641841,"end":40642117,"strand":-1,"description":"immunoglobulin kappa variable 1/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49466]"}, {"versioned_ensembl_gene_id":"ENSG00000248262.1","gene_symbol":"AC108037.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11914667,"end":11919688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164134.12","gene_symbol":"NAA15","gene_name":"N(alpha)-acetyltransferase 15, NatA auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:30782]","synonyms":"TBDN100,NATH,NARG1,FLJ13340","biotype":"protein_coding","ncbi_id":"80155","summary":"N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes the auxillary subunit of the N-terminal acetyltransferase A (NatA) complex. [provided by RefSeq, Jan 2017]","start":139301455,"end":139420033,"strand":1,"description":"N(alpha)-acetyltransferase 15, NatA auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:30782]"}, {"versioned_ensembl_gene_id":"ENSG00000281186.1","gene_symbol":"LINC00706","gene_name":"long intergenic non-protein coding RNA 706 [Source:NCBI gene;Acc:100652997]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652997","summary":null,"start":6774307,"end":6779180,"strand":-1,"description":"long intergenic non-protein coding RNA 706 [Source:NCBI gene;Acc:100652997]"}, {"versioned_ensembl_gene_id":"ENSG00000223784.1","gene_symbol":"LINP1","gene_name":"lncRNA in non-homologous end joining pathway 1 [Source:HGNC Symbol;Acc:HGNC:53170]","synonyms":null,"biotype":"lincRNA","ncbi_id":"108570035","summary":null,"start":6737382,"end":6739026,"strand":1,"description":"lncRNA in non-homologous end joining pathway 1 [Source:HGNC Symbol;Acc:HGNC:53170]"}, {"versioned_ensembl_gene_id":"ENSG00000225756.1","gene_symbol":"DBH-AS1","gene_name":"DBH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24155]","synonyms":"NCRNA00118,BPR","biotype":"antisense_RNA","ncbi_id":"138948","summary":null,"start":133654586,"end":133657313,"strand":-1,"description":"DBH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24155]"}, {"versioned_ensembl_gene_id":"ENSG00000108306.11","gene_symbol":"FBXL20","gene_name":"F-box and leucine rich repeat protein 20 [Source:HGNC Symbol;Acc:HGNC:24679]","synonyms":"MGC15482,Fbl20,Fbl2","biotype":"protein_coding","ncbi_id":"84961","summary":"Members of the F-box protein family, such as FBXL20, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":39252644,"end":39402523,"strand":-1,"description":"F-box and leucine rich repeat protein 20 [Source:HGNC Symbol;Acc:HGNC:24679]"}, {"versioned_ensembl_gene_id":"ENSG00000233138.1","gene_symbol":"AL023584.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142748443,"end":142753759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225948.2","gene_symbol":"AL158210.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6618716,"end":6625346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227737.3","gene_symbol":"OR8B1P","gene_name":"olfactory receptor family 8 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8470]","synonyms":"OR8B11P,OR11-561","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"8582","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124365465,"end":124367298,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8470]"}, {"versioned_ensembl_gene_id":"ENSG00000237851.1","gene_symbol":"AL023584.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142788123,"end":142794086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255030.1","gene_symbol":"AP001804.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":124357560,"end":124358469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196341.3","gene_symbol":"OR8D1","gene_name":"olfactory receptor family 8 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:8481]","synonyms":"OST004,OR8D3","biotype":"protein_coding","ncbi_id":"283159","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124302831,"end":124315099,"strand":-1,"description":"olfactory receptor family 8 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:8481]"}, {"versioned_ensembl_gene_id":"ENSG00000224677.1","gene_symbol":"PDIA3P2","gene_name":"protein disulfide isomerase family A member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49403]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481687","summary":null,"start":43649123,"end":43649280,"strand":1,"description":"protein disulfide isomerase family A member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49403]"}, {"versioned_ensembl_gene_id":"ENSG00000236432.7","gene_symbol":"AC097662.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":227221052,"end":227325201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255116.2","gene_symbol":"SLC5A4P1","gene_name":"solute carrier family 5 member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45041]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422550","summary":null,"start":124273970,"end":124274581,"strand":1,"description":"solute carrier family 5 member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45041]"}, {"versioned_ensembl_gene_id":"ENSG00000251009.2","gene_symbol":"AC133961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25864881,"end":25869550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250541.1","gene_symbol":"AC092436.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25770266,"end":25773577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255298.3","gene_symbol":"OR8G5","gene_name":"olfactory receptor family 8 subfamily G member 5 [Source:HGNC Symbol;Acc:HGNC:19622]","synonyms":"OR8G6,OR8G5P","biotype":"protein_coding","ncbi_id":"219865","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124256376,"end":124266218,"strand":1,"description":"olfactory receptor family 8 subfamily G member 5 [Source:HGNC Symbol;Acc:HGNC:19622]"}, {"versioned_ensembl_gene_id":"ENSG00000197849.6","gene_symbol":"OR8G1","gene_name":"olfactory receptor family 8 subfamily G member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8484]","synonyms":"HSTPCR25,TPCR25,OR8G1P","biotype":"protein_coding","ncbi_id":"26494","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This family member represents a polymorphic pseudogene, whereby some individuals have a functional allele that encodes a full-length protein, while others have a non-functional allele due to the presence of an early stop codon and a 3' end deletion. [provided by RefSeq, Feb 2014]","start":124241095,"end":124254364,"strand":1,"description":"olfactory receptor family 8 subfamily G member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8484]"}, {"versioned_ensembl_gene_id":"ENSG00000121152.9","gene_symbol":"NCAPH","gene_name":"non-SMC condensin I complex subunit H [Source:HGNC Symbol;Acc:HGNC:1112]","synonyms":"hCAP-H,CAP-H,BRRN1","biotype":"protein_coding","ncbi_id":"23397","summary":"This gene encodes a member of the barr gene family and a regulatory subunit of the condensin complex. This complex is required for the conversion of interphase chromatin into condensed chromosomes. The protein encoded by this gene is associated with mitotic chromosomes, except during the early phase of chromosome condensation. During interphase, the protein has a distinct punctate nucleolar localization. Alternatively spliced transcript variants encoding different proteins have been described. [provided by RefSeq, Jul 2013]","start":96335787,"end":96373845,"strand":1,"description":"non-SMC condensin I complex subunit H [Source:HGNC Symbol;Acc:HGNC:1112]"}, {"versioned_ensembl_gene_id":"ENSG00000276316.1","gene_symbol":"OR8G7P","gene_name":"olfactory receptor family 8 subfamily G member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:19625]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"282786","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124238420,"end":124239486,"strand":1,"description":"olfactory receptor family 8 subfamily G member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:19625]"}, {"versioned_ensembl_gene_id":"ENSG00000181214.7","gene_symbol":"OR8G2P","gene_name":"olfactory receptor family 8 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8485]","synonyms":"TPCR120,ORL486,ORL206,OR8G4,OR8G2,HSTPCR120","biotype":"unprocessed_pseudogene","ncbi_id":"26492","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124224732,"end":124225639,"strand":1,"description":"olfactory receptor family 8 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8485]"}, {"versioned_ensembl_gene_id":"ENSG00000261665.2","gene_symbol":"TUBAP4","gene_name":"tubulin alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44569]","synonyms":"TUBA8P2","biotype":"transcribed_processed_pseudogene","ncbi_id":"106479041","summary":null,"start":83739784,"end":83740199,"strand":1,"description":"tubulin alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44569]"}, {"versioned_ensembl_gene_id":"ENSG00000249839.1","gene_symbol":"AC011330.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43663654,"end":43684339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274128.1","gene_symbol":"AC027807.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":83962176,"end":83962583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132768.13","gene_symbol":"DPH2","gene_name":"DPH2 homolog [Source:HGNC Symbol;Acc:HGNC:3004]","synonyms":"DPH2L2","biotype":"protein_coding","ncbi_id":"1802","summary":"This gene is one of two human genes similar to the yeast gene dph2. The yeast gene was identified by its ability to complement a diphthamide mutant strain, and thus probably functions in diphthamide biosynthesis. Diphthamide is a post-translationally modified histidine residue present in elongation factor 2 (EF2) that is the target of diphtheria toxin ADP-ribosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":43970000,"end":43973369,"strand":1,"description":"DPH2 homolog [Source:HGNC Symbol;Acc:HGNC:3004]"}, {"versioned_ensembl_gene_id":"ENSG00000224933.2","gene_symbol":"LINC01034","gene_name":"long intergenic non-protein coding RNA 1034 [Source:HGNC Symbol;Acc:HGNC:49021]","synonyms":"TCONS_00021570","biotype":"lincRNA","ncbi_id":"106144601","summary":null,"start":76013023,"end":76014501,"strand":-1,"description":"long intergenic non-protein coding RNA 1034 [Source:HGNC Symbol;Acc:HGNC:49021]"}, {"versioned_ensembl_gene_id":"ENSG00000248749.1","gene_symbol":"AC104063.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84371393,"end":84380189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268987.1","gene_symbol":"AC011462.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41399372,"end":41400365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134962.6","gene_symbol":"KLB","gene_name":"klotho beta [Source:HGNC Symbol;Acc:HGNC:15527]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152831","summary":null,"start":39406853,"end":39451536,"strand":1,"description":"klotho beta [Source:HGNC Symbol;Acc:HGNC:15527]"}, {"versioned_ensembl_gene_id":"ENSG00000221886.3","gene_symbol":"ZBED8","gene_name":"zinc finger BED-type containing 8 [Source:HGNC Symbol;Acc:HGNC:30804]","synonyms":"C5orf54,Buster3","biotype":"protein_coding","ncbi_id":"63920","summary":null,"start":160393148,"end":160400097,"strand":-1,"description":"zinc finger BED-type containing 8 [Source:HGNC Symbol;Acc:HGNC:30804]"}, {"versioned_ensembl_gene_id":"ENSG00000261253.2","gene_symbol":"AC137932.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":89321133,"end":89325110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010818.9","gene_symbol":"HIVEP2","gene_name":"human immunodeficiency virus type I enhancer binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4921]","synonyms":"ZNF40B,ZAS2,Schnurri-2,MIBP1,MBP-2,HIV-EP2","biotype":"protein_coding","ncbi_id":"3097","summary":"This gene encodes a member of a family of closely related, large, zinc finger-containing transcription factors. The encoded protein regulates transcription by binding to regulatory regions of various cellular and viral genes that maybe involved in growth, development and metastasis. The protein contains the ZAS domain comprised of two widely separated regions of zinc finger motifs, a stretch of highly acidic amino acids and a serine/threonine-rich sequence. [provided by RefSeq, Nov 2012]","start":142751467,"end":142956698,"strand":-1,"description":"human immunodeficiency virus type I enhancer binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4921]"}, {"versioned_ensembl_gene_id":"ENSG00000197111.15","gene_symbol":"PCBP2","gene_name":"poly(rC) binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8648]","synonyms":"HNRPE2,HNRNPE2,hnRNP-E2","biotype":"protein_coding","ncbi_id":"5094","summary":"The protein encoded by this gene appears to be multifunctional. Along with PCBP-1 and hnRNPK, it is one of the major cellular poly(rC)-binding proteins. The encoded protein contains three K-homologous (KH) domains which may be involved in RNA binding. Together with PCBP-1, this protein also functions as a translational coactivator of poliovirus RNA via a sequence-specific interaction with stem-loop IV of the IRES, promoting poliovirus RNA replication by binding to its 5'-terminal cloverleaf structure. It has also been implicated in translational control of the 15-lipoxygenase mRNA, human papillomavirus type 16 L2 mRNA, and hepatitis A virus RNA. The encoded protein is also suggested to play a part in formation of a sequence-specific alpha-globin mRNP complex which is associated with alpha-globin mRNA stability. This multiexon structural mRNA is thought to be retrotransposed to generate PCBP-1, an intronless gene with functions similar to that of PCBP2. This gene and PCBP-1 have paralogous genes (PCBP3 and PCBP4) which are thought to have arisen as a result of duplication events of entire genes. This gene also has two processed pseudogenes (PCBP2P1 and PCBP2P2). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2018]","start":53452102,"end":53481162,"strand":1,"description":"poly(rC) binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8648]"}, {"versioned_ensembl_gene_id":"ENSG00000250546.5","gene_symbol":"AC079160.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":83796436,"end":84293412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176798.2","gene_symbol":"OR51L1","gene_name":"olfactory receptor family 51 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14759]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119682","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4994851,"end":5005536,"strand":1,"description":"olfactory receptor family 51 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14759]"}, {"versioned_ensembl_gene_id":"ENSG00000164591.13","gene_symbol":"MYOZ3","gene_name":"myozenin 3 [Source:HGNC Symbol;Acc:HGNC:18565]","synonyms":"FRP3,CS3,CS-3","biotype":"protein_coding","ncbi_id":"91977","summary":"The protein encoded by this gene is specifically expressed in the skeletal muscle, and belongs to the myozenin family. Members of this family function as calcineurin-interacting proteins that help tether calcineurin to the sarcomere of cardiac and skeletal muscle. They play an important role in modulation of calcineurin signaling. [provided by RefSeq, Apr 2012]","start":150660874,"end":150679365,"strand":1,"description":"myozenin 3 [Source:HGNC Symbol;Acc:HGNC:18565]"}, {"versioned_ensembl_gene_id":"ENSG00000253666.1","gene_symbol":"AP000424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100475675,"end":100501148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266469.1","gene_symbol":"AC005288.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39401793,"end":39406233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250309.2","gene_symbol":"AC008453.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150670658,"end":150672390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278924.1","gene_symbol":"AC078883.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":172423807,"end":172424173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161513.11","gene_symbol":"FDXR","gene_name":"ferredoxin reductase [Source:HGNC Symbol;Acc:HGNC:3642]","synonyms":"ADXR","biotype":"protein_coding","ncbi_id":"2232","summary":"This gene encodes a mitochondrial flavoprotein that initiates electron transport for cytochromes P450 receiving electrons from NADPH. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2012]","start":74862497,"end":74873031,"strand":-1,"description":"ferredoxin reductase [Source:HGNC Symbol;Acc:HGNC:3642]"}, {"versioned_ensembl_gene_id":"ENSG00000269776.1","gene_symbol":"DPPA5P1","gene_name":"developmental pluripotency associated 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646382","summary":null,"start":52425863,"end":52426202,"strand":-1,"description":"developmental pluripotency associated 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43752]"}, {"versioned_ensembl_gene_id":"ENSG00000214511.3","gene_symbol":"HIGD1C","gene_name":"HIG1 hypoxia inducible domain family member 1C [Source:HGNC Symbol;Acc:HGNC:28044]","synonyms":"Gm921","biotype":"protein_coding","ncbi_id":"613227","summary":null,"start":50953922,"end":50970506,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1C [Source:HGNC Symbol;Acc:HGNC:28044]"}, {"versioned_ensembl_gene_id":"ENSG00000115844.10","gene_symbol":"DLX2","gene_name":"distal-less homeobox 2 [Source:HGNC Symbol;Acc:HGNC:2915]","synonyms":"TES-1","biotype":"protein_coding","ncbi_id":"1746","summary":"Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. The DLX proteins are postulated to play a role in forebrain and craniofacial development. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 2. [provided by RefSeq, Jul 2008]","start":172099439,"end":172102900,"strand":-1,"description":"distal-less homeobox 2 [Source:HGNC Symbol;Acc:HGNC:2915]"}, {"versioned_ensembl_gene_id":"ENSG00000164609.9","gene_symbol":"SLU7","gene_name":"SLU7 homolog, splicing factor [Source:HGNC Symbol;Acc:HGNC:16939]","synonyms":"9G8","biotype":"protein_coding","ncbi_id":"10569","summary":"Pre-mRNA splicing occurs in two sequential transesterification steps. The protein encoded by this gene is a splicing factor that has been found to be essential during the second catalytic step in the pre-mRNA splicing process. It associates with the spliceosome and contains a zinc knuckle motif that is found in other splicing factors and is involved in protein-nucleic acid and protein-protein interactions. [provided by RefSeq, Jul 2008]","start":160401641,"end":160421711,"strand":-1,"description":"SLU7 homolog, splicing factor [Source:HGNC Symbol;Acc:HGNC:16939]"}, {"versioned_ensembl_gene_id":"ENSG00000249171.1","gene_symbol":"AC021192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83668510,"end":83731755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196990.8","gene_symbol":"FAM163B","gene_name":"family with sequence similarity 163 member B [Source:HGNC Symbol;Acc:HGNC:33277]","synonyms":"C9orf166","biotype":"protein_coding","ncbi_id":"642968","summary":null,"start":133578415,"end":133586197,"strand":-1,"description":"family with sequence similarity 163 member B [Source:HGNC Symbol;Acc:HGNC:33277]"}, {"versioned_ensembl_gene_id":"ENSG00000261692.1","gene_symbol":"AC092120.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89420075,"end":89422226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227074.11","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"NG23,C6orf26","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31744980,"end":31747032,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000250317.8","gene_symbol":"SMIM20","gene_name":"small integral membrane protein 20 [Source:HGNC Symbol;Acc:HGNC:37260]","synonyms":"PNX,C4orf52","biotype":"protein_coding","ncbi_id":"389203","summary":null,"start":25861830,"end":25929874,"strand":1,"description":"small integral membrane protein 20 [Source:HGNC Symbol;Acc:HGNC:37260]"}, {"versioned_ensembl_gene_id":"ENSG00000161381.13","gene_symbol":"PLXDC1","gene_name":"plexin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20945]","synonyms":"TEM7,TEM3","biotype":"protein_coding","ncbi_id":"57125","summary":null,"start":39063303,"end":39154394,"strand":-1,"description":"plexin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20945]"}, {"versioned_ensembl_gene_id":"ENSG00000172007.5","gene_symbol":"RAB33B","gene_name":"RAB33B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16075]","synonyms":"DKFZP434G099","biotype":"protein_coding","ncbi_id":"83452","summary":"This gene encodes a small GTP-binding protein of the Rab GTPase family, whose members function in vesicle transport during protein secretion and endocytosis. Rab GTPases are active, membrane-associated proteins that recruit effector proteins in the GTP-bound state and inactive cytosolic proteins when in a GDP-bound state. The protein encoded by this gene is ubiquitously expressed and has been implicated in Golgi to endoplasmic reticulum cycling of Golgi enzymes. In addition, this protein regulates Golgi homeostasis and coordinates intra-Golgi retrograde trafficking. Allelic variants in this gene have been associated with Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia 2, which are autosomal recessive spondyloepimetaphyseal dysplasias characterized by skeletal abnormalities. [provided by RefSeq, Sep 2016]","start":139453232,"end":139476609,"strand":1,"description":"RAB33B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16075]"}, {"versioned_ensembl_gene_id":"ENSG00000271596.1","gene_symbol":"AC008121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50949117,"end":50949384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230846.1","gene_symbol":"AL158154.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81928021,"end":81931368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077348.8","gene_symbol":"EXOSC5","gene_name":"exosome component 5 [Source:HGNC Symbol;Acc:HGNC:24662]","synonyms":"Rrp46p,RRP46,RRP41B,p12B,MGC12901,hRrp46p","biotype":"protein_coding","ncbi_id":"56915","summary":null,"start":41386374,"end":41397479,"strand":-1,"description":"exosome component 5 [Source:HGNC Symbol;Acc:HGNC:24662]"}, {"versioned_ensembl_gene_id":"ENSG00000267559.5","gene_symbol":"AL158154.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81930226,"end":81977089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277744.1","gene_symbol":"AC011462.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41373971,"end":41374419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189357.8","gene_symbol":"SPATA31D4","gene_name":"SPATA31 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:38601]","synonyms":"FLJ43859,FAM75D4","biotype":"protein_coding","ncbi_id":"389761","summary":null,"start":81928514,"end":81934948,"strand":1,"description":"SPATA31 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:38601]"}, {"versioned_ensembl_gene_id":"ENSG00000171992.12","gene_symbol":"SYNPO","gene_name":"synaptopodin [Source:HGNC Symbol;Acc:HGNC:30672]","synonyms":"KIAA1029","biotype":"protein_coding","ncbi_id":"11346","summary":"Synaptopodin is an actin-associated protein that may play a role in actin-based cell shape and motility. The name synaptopodin derives from the protein's associations with postsynaptic densities and dendritic spines and with renal podocytes (Mundel et al., 1997 [PubMed 9314539]).[supplied by OMIM, Mar 2008]","start":150601080,"end":150659220,"strand":1,"description":"synaptopodin [Source:HGNC Symbol;Acc:HGNC:30672]"}, {"versioned_ensembl_gene_id":"ENSG00000266560.5","gene_symbol":"AF274856.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":152114994,"end":152138556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255425.5","gene_symbol":"OR8G3P","gene_name":"olfactory receptor family 8 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14698]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387815","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124211707,"end":124215828,"strand":1,"description":"olfactory receptor family 8 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14698]"}, {"versioned_ensembl_gene_id":"ENSG00000248863.2","gene_symbol":"AC097376.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":139426299,"end":139430884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239426.4","gene_symbol":"OR8F1P","gene_name":"olfactory receptor family 8 subfamily F member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14691]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390269","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124207183,"end":124208112,"strand":1,"description":"olfactory receptor family 8 subfamily F member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14691]"}, {"versioned_ensembl_gene_id":"ENSG00000186910.3","gene_symbol":"SERPINA11","gene_name":"serpin family A member 11 [Source:HGNC Symbol;Acc:HGNC:19193]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256394","summary":null,"start":94442464,"end":94452790,"strand":-1,"description":"serpin family A member 11 [Source:HGNC Symbol;Acc:HGNC:19193]"}, {"versioned_ensembl_gene_id":"ENSG00000167522.14","gene_symbol":"ANKRD11","gene_name":"ankyrin repeat domain 11 [Source:HGNC Symbol;Acc:HGNC:21316]","synonyms":"T13,LZ16","biotype":"protein_coding","ncbi_id":"29123","summary":"This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012]","start":89267627,"end":89490561,"strand":-1,"description":"ankyrin repeat domain 11 [Source:HGNC Symbol;Acc:HGNC:21316]"}, {"versioned_ensembl_gene_id":"ENSG00000132432.13","gene_symbol":"SEC61G","gene_name":"Sec61 translocon gamma subunit [Source:HGNC Symbol;Acc:HGNC:18277]","synonyms":"SSS1","biotype":"protein_coding","ncbi_id":"23480","summary":"The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. Oligomers of the Sec61 complex form a transmembrane channel where proteins are translocated across and integrated into the ER membrane. This complex consists of three membrane proteins- alpha, beta, and gamma. This gene encodes the gamma-subunit protein. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":54752250,"end":54759974,"strand":-1,"description":"Sec61 translocon gamma subunit [Source:HGNC Symbol;Acc:HGNC:18277]"}, {"versioned_ensembl_gene_id":"ENSG00000196403.4","gene_symbol":"OR10D1P","gene_name":"olfactory receptor family 10 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8166]","synonyms":"HTPCRX03,OST074,OR10D2P","biotype":"unprocessed_pseudogene","ncbi_id":"26541","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124158421,"end":124159356,"strand":1,"description":"olfactory receptor family 10 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8166]"}, {"versioned_ensembl_gene_id":"ENSG00000227856.1","gene_symbol":"SAPCD1-AS1","gene_name":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]","synonyms":"C6orf26-AS1","biotype":"processed_transcript","ncbi_id":"104413891","summary":null,"start":31746491,"end":31747769,"strand":-1,"description":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]"}, {"versioned_ensembl_gene_id":"ENSG00000224404.1","gene_symbol":"Z68323.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34208141,"end":34209262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240632.6","gene_symbol":"SPATA31D5P","gene_name":"SPATA31 subfamily D member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38602]","synonyms":"FAM75D5P,FAM75D5,FLJ43950","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"347127","summary":null,"start":81913437,"end":81919926,"strand":1,"description":"SPATA31 subfamily D member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38602]"}, {"versioned_ensembl_gene_id":"ENSG00000006059.3","gene_symbol":"KRT33A","gene_name":"keratin 33A [Source:HGNC Symbol;Acc:HGNC:6450]","synonyms":"KRTHA3A,Krt1-3,Ha-3I","biotype":"protein_coding","ncbi_id":"3883","summary":"This gene encodes a member of the keratin gene family. This gene is one of multiple type I hair keratin genes that are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. As a type I hair keratin, the encoded protein is an acidic protein which heterodimerizes with type II keratins to form hair and nails. There are two isoforms of this protein, encoded by two separate genes, keratin 33A and keratin 33B. [provided by RefSeq, May 2012]","start":41346092,"end":41350812,"strand":-1,"description":"keratin 33A [Source:HGNC Symbol;Acc:HGNC:6450]"}, {"versioned_ensembl_gene_id":"ENSG00000108516.5","gene_symbol":"AC003958.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41334632,"end":41335733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186860.4","gene_symbol":"KRTAP17-1","gene_name":"keratin associated protein 17-1 [Source:HGNC Symbol;Acc:HGNC:18917]","synonyms":"KAP17.1","biotype":"protein_coding","ncbi_id":"83902","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41314917,"end":41315695,"strand":-1,"description":"keratin associated protein 17-1 [Source:HGNC Symbol;Acc:HGNC:18917]"}, {"versioned_ensembl_gene_id":"ENSG00000212657.1","gene_symbol":"KRTAP16-1","gene_name":"keratin associated protein 16-1 [Source:HGNC Symbol;Acc:HGNC:18916]","synonyms":"KAP16.1","biotype":"protein_coding","ncbi_id":"100505753","summary":null,"start":41307700,"end":41309253,"strand":-1,"description":"keratin associated protein 16-1 [Source:HGNC Symbol;Acc:HGNC:18916]"}, {"versioned_ensembl_gene_id":"ENSG00000212658.1","gene_symbol":"KRTAP29-1","gene_name":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]","synonyms":"KAP29.2","biotype":"protein_coding","ncbi_id":"100533177","summary":null,"start":41301826,"end":41302851,"strand":-1,"description":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]"}, {"versioned_ensembl_gene_id":"ENSG00000228008.1","gene_symbol":"AC105935.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49903845,"end":49916937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158423.16","gene_symbol":"RIBC1","gene_name":"RIB43A domain with coiled-coils 1 [Source:HGNC Symbol;Acc:HGNC:26537]","synonyms":"FLJ32783","biotype":"protein_coding","ncbi_id":"158787","summary":null,"start":53422690,"end":53431120,"strand":1,"description":"RIB43A domain with coiled-coils 1 [Source:HGNC Symbol;Acc:HGNC:26537]"}, {"versioned_ensembl_gene_id":"ENSG00000237183.1","gene_symbol":"KRTAP9-10P","gene_name":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480422","summary":null,"start":41280604,"end":41280810,"strand":1,"description":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]"}, {"versioned_ensembl_gene_id":"ENSG00000180386.7","gene_symbol":"KRTAP9-7","gene_name":"keratin associated protein 9-7 [Source:HGNC Symbol;Acc:HGNC:18915]","synonyms":"KRTAP9L1,KAP9.7","biotype":"protein_coding","ncbi_id":"100505724","summary":null,"start":41275659,"end":41276697,"strand":1,"description":"keratin associated protein 9-7 [Source:HGNC Symbol;Acc:HGNC:18915]"}, {"versioned_ensembl_gene_id":"ENSG00000229351.1","gene_symbol":"KRTAP9-11P","gene_name":"keratin associated protein 9-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18918]","synonyms":"KRTAP9P1,KAP9A","biotype":"unprocessed_pseudogene","ncbi_id":"85347","summary":null,"start":41271311,"end":41271835,"strand":1,"description":"keratin associated protein 9-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18918]"}, {"versioned_ensembl_gene_id":"ENSG00000197859.9","gene_symbol":"ADAMTSL2","gene_name":"ADAMTS like 2 [Source:HGNC Symbol;Acc:HGNC:14631]","synonyms":"KIAA0605","biotype":"protein_coding","ncbi_id":"9719","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily. It is a secreted glycoprotein that binds the cell surface and extracellular matrix; it also interacts with latent transforming growth factor beta binding protein 1. Mutations in this gene have been associated with geleophysic dysplasia. [provided by RefSeq, Feb 2009]","start":133532164,"end":133575519,"strand":1,"description":"ADAMTS like 2 [Source:HGNC Symbol;Acc:HGNC:14631]"}, {"versioned_ensembl_gene_id":"ENSG00000225432.1","gene_symbol":"BX247947.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497985,"end":29511032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231000.3","gene_symbol":"BX247947.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489747,"end":29490152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161509.13","gene_symbol":"GRIN2C","gene_name":"glutamate ionotropic receptor NMDA type subunit 2C [Source:HGNC Symbol;Acc:HGNC:4587]","synonyms":"NMDAR2C,GluN2C","biotype":"protein_coding","ncbi_id":"2905","summary":"This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D), forming a channel that is permeable to calcium, potassium, and sodium, and whose properties are determined by subunit composition. Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease, Alzheimer's disease, depression, and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":74842023,"end":74861504,"strand":-1,"description":"glutamate ionotropic receptor NMDA type subunit 2C [Source:HGNC Symbol;Acc:HGNC:4587]"}, {"versioned_ensembl_gene_id":"ENSG00000232204.1","gene_symbol":"TET1P1","gene_name":"tet methylcytosine dioxygenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33586]","synonyms":"CXXC6P1","biotype":"processed_pseudogene","ncbi_id":"441662","summary":null,"start":87890172,"end":87892472,"strand":-1,"description":"tet methylcytosine dioxygenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33586]"}, {"versioned_ensembl_gene_id":"ENSG00000060982.14","gene_symbol":"BCAT1","gene_name":"branched chain amino acid transaminase 1 [Source:HGNC Symbol;Acc:HGNC:976]","synonyms":"BCT1","biotype":"protein_coding","ncbi_id":"586","summary":"This gene encodes the cytosolic form of the enzyme branched-chain amino acid transaminase. This enzyme catalyzes the reversible transamination of branched-chain alpha-keto acids to branched-chain L-amino acids essential for cell growth. Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia. As there is also a gene encoding a mitochondrial form of this enzyme, mutations in either gene may contribute to these disorders. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2010]","start":24810022,"end":24949459,"strand":-1,"description":"branched chain amino acid transaminase 1 [Source:HGNC Symbol;Acc:HGNC:976]"}, {"versioned_ensembl_gene_id":"ENSG00000278969.1","gene_symbol":"AC026310.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24902309,"end":24904681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256482.1","gene_symbol":"AC023796.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24830421,"end":24836558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223404.3","gene_symbol":"LINC00397","gene_name":"long intergenic non-protein coding RNA 397 [Source:HGNC Symbol;Acc:HGNC:42725]","synonyms":"TCONS_00021582","biotype":"lincRNA","ncbi_id":"101930749","summary":null,"start":87801036,"end":87803808,"strand":-1,"description":"long intergenic non-protein coding RNA 397 [Source:HGNC Symbol;Acc:HGNC:42725]"}, {"versioned_ensembl_gene_id":"ENSG00000230698.1","gene_symbol":"AC105935.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49899302,"end":49903757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105771.13","gene_symbol":"SMG9","gene_name":"SMG9, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:25763]","synonyms":"FLJ12886,C19orf61","biotype":"protein_coding","ncbi_id":"56006","summary":"This gene encodes a regulatory subunit of the SMG1 complex, which plays a critical role in nonsense-mediated mRNA decay (NMD). Binding of the encoded protein to the SMG1 complex kinase scaffold protein results in the inhibition of its kinase activity. Mutations in this gene cause a multiple congenital anomaly syndrome in human patients, characterized by brain malformation, congenital heart disease and other features. [provided by RefSeq, Jul 2016]","start":43727992,"end":43754990,"strand":-1,"description":"SMG9, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:25763]"}, {"versioned_ensembl_gene_id":"ENSG00000254890.1","gene_symbol":"AP003049.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109486968,"end":109487424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117322.17","gene_symbol":"CR2","gene_name":"complement C3d receptor 2 [Source:HGNC Symbol;Acc:HGNC:2336]","synonyms":"CD21,C3DR","biotype":"protein_coding","ncbi_id":"1380","summary":"This gene encodes a membrane protein, which functions as a receptor for Epstein-Barr virus (EBV) binding on B and T lymphocytes. Genetic variations in this gene are associated with susceptibility to systemic lupus erythematosus type 9 (SLEB9). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":207454230,"end":207489895,"strand":1,"description":"complement C3d receptor 2 [Source:HGNC Symbol;Acc:HGNC:2336]"}, {"versioned_ensembl_gene_id":"ENSG00000186377.7","gene_symbol":"CYP4X1","gene_name":"cytochrome P450 family 4 subfamily X member 1 [Source:HGNC Symbol;Acc:HGNC:20244]","synonyms":"MGC40051","biotype":"protein_coding","ncbi_id":"260293","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes and is located within a cluster of genes belonging to this superfamily on chromosome 1. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The expression pattern of a similar rat protein suggests that this protein may be involved in neurovascular function in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":47023568,"end":47050751,"strand":1,"description":"cytochrome P450 family 4 subfamily X member 1 [Source:HGNC Symbol;Acc:HGNC:20244]"}, {"versioned_ensembl_gene_id":"ENSG00000167555.13","gene_symbol":"ZNF528","gene_name":"zinc finger protein 528 [Source:HGNC Symbol;Acc:HGNC:29384]","synonyms":"KIAA1827","biotype":"protein_coding","ncbi_id":"84436","summary":null,"start":52397849,"end":52418412,"strand":1,"description":"zinc finger protein 528 [Source:HGNC Symbol;Acc:HGNC:29384]"}, {"versioned_ensembl_gene_id":"ENSG00000203334.4","gene_symbol":"AP003027.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108957718,"end":108959797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277640.1","gene_symbol":"AL445647.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87765752,"end":87765881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228541.1","gene_symbol":"AC093159.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62463127,"end":62464070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270335.1","gene_symbol":"AC093159.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62348948,"end":62350739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228195.2","gene_symbol":"RPL5P27","gene_name":"ribosomal protein L5 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36172]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129998","summary":null,"start":116749905,"end":116751261,"strand":1,"description":"ribosomal protein L5 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36172]"}, {"versioned_ensembl_gene_id":"ENSG00000109066.13","gene_symbol":"TMEM104","gene_name":"transmembrane protein 104 [Source:HGNC Symbol;Acc:HGNC:25984]","synonyms":"FLJ20255,FLJ00021","biotype":"protein_coding","ncbi_id":"54868","summary":null,"start":74776483,"end":74839779,"strand":1,"description":"transmembrane protein 104 [Source:HGNC Symbol;Acc:HGNC:25984]"}, {"versioned_ensembl_gene_id":"ENSG00000261290.1","gene_symbol":"CYP4A44P","gene_name":"cytochrome P450 family 4 subfamily A member 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:42416]","synonyms":"CYP4A-se4[2]","biotype":"unprocessed_pseudogene","ncbi_id":"106481791","summary":null,"start":47002995,"end":47003148,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:42416]"}, {"versioned_ensembl_gene_id":"ENSG00000187616.4","gene_symbol":"MYMK","gene_name":"myomaker, myoblast fusion factor [Source:HGNC Symbol;Acc:HGNC:33778]","synonyms":"TMEM8C,TMEM226","biotype":"protein_coding","ncbi_id":"389827","summary":null,"start":133514586,"end":133528612,"strand":-1,"description":"myomaker, myoblast fusion factor [Source:HGNC Symbol;Acc:HGNC:33778]"}, {"versioned_ensembl_gene_id":"ENSG00000275650.4","gene_symbol":"TTYH1","gene_name":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57348","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-independent, volume-sensitive large conductance chloride(-) channel. Three transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jan 2011]","start":54423352,"end":54444827,"strand":1,"description":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]"}, {"versioned_ensembl_gene_id":"ENSG00000259832.1","gene_symbol":"CYP4A26P","gene_name":"cytochrome P450 family 4 subfamily A member 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:39980]","synonyms":"CYP4A-se1[12]","biotype":"unprocessed_pseudogene","ncbi_id":"107080641","summary":null,"start":46967679,"end":46967874,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:39980]"}, {"versioned_ensembl_gene_id":"ENSG00000274067.1","gene_symbol":"FP885919.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40481559,"end":40497591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272515.1","gene_symbol":"AL355578.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87607907,"end":87609234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269834.5","gene_symbol":"ZNF528-AS1","gene_name":"ZNF528 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51305]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"102724105","summary":null,"start":52388842,"end":52397766,"strand":-1,"description":"ZNF528 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51305]"}, {"versioned_ensembl_gene_id":"ENSG00000072501.17","gene_symbol":"SMC1A","gene_name":"structural maintenance of chromosomes 1A [Source:HGNC Symbol;Acc:HGNC:11111]","synonyms":"SB1.8,KIAA0178,DXS423E,Smcb,SMC1L1","biotype":"protein_coding","ncbi_id":"8243","summary":"Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":53374149,"end":53422728,"strand":-1,"description":"structural maintenance of chromosomes 1A [Source:HGNC Symbol;Acc:HGNC:11111]"}, {"versioned_ensembl_gene_id":"ENSG00000276500.1","gene_symbol":"BMS1P14","gene_name":"BMS1, ribosome biogenesis factor pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49159]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728034","summary":null,"start":40505399,"end":40566281,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49159]"}, {"versioned_ensembl_gene_id":"ENSG00000228824.6","gene_symbol":"MIR4500HG","gene_name":"MIR4500 host gene [Source:HGNC Symbol;Acc:HGNC:42773]","synonyms":null,"biotype":"lincRNA","ncbi_id":"642345","summary":null,"start":87427214,"end":87671259,"strand":-1,"description":"MIR4500 host gene [Source:HGNC Symbol;Acc:HGNC:42773]"}, {"versioned_ensembl_gene_id":"ENSG00000258646.1","gene_symbol":"AL049780.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75004719,"end":75008481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233528.4","gene_symbol":"LINC00430","gene_name":"long intergenic non-protein coding RNA 430 [Source:HGNC Symbol;Acc:HGNC:42765]","synonyms":"TCONS_00021581","biotype":"lincRNA","ncbi_id":"106144533","summary":null,"start":86909586,"end":86937108,"strand":1,"description":"long intergenic non-protein coding RNA 430 [Source:HGNC Symbol;Acc:HGNC:42765]"}, {"versioned_ensembl_gene_id":"ENSG00000257446.3","gene_symbol":"ZNF878","gene_name":"zinc finger protein 878 [Source:HGNC Symbol;Acc:HGNC:37246]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729747","summary":null,"start":12043805,"end":12052939,"strand":-1,"description":"zinc finger protein 878 [Source:HGNC Symbol;Acc:HGNC:37246]"}, {"versioned_ensembl_gene_id":"ENSG00000011405.13","gene_symbol":"PIK3C2A","gene_name":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha [Source:HGNC Symbol;Acc:HGNC:8971]","synonyms":"PI3K-C2alpha","biotype":"protein_coding","ncbi_id":"5286","summary":"The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. The PI3-kinase activity of this protein is not sensitive to nanomolar levels of the inhibitor wortmanin. This protein was shown to be able to be activated by insulin and may be involved in integrin-dependent signaling. [provided by RefSeq, Jul 2008]","start":17077730,"end":17207983,"strand":-1,"description":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha [Source:HGNC Symbol;Acc:HGNC:8971]"}, {"versioned_ensembl_gene_id":"ENSG00000164713.9","gene_symbol":"BRI3","gene_name":"brain protein I3 [Source:HGNC Symbol;Acc:HGNC:1109]","synonyms":null,"biotype":"protein_coding","ncbi_id":"25798","summary":null,"start":98252379,"end":98310441,"strand":1,"description":"brain protein I3 [Source:HGNC Symbol;Acc:HGNC:1109]"}, {"versioned_ensembl_gene_id":"ENSG00000070614.14","gene_symbol":"NDST1","gene_name":"N-deacetylase and N-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:7680]","synonyms":"NST1,HSST","biotype":"protein_coding","ncbi_id":"3340","summary":"This gene encodes a member of the heparan sulfate/heparin GlcNAc N-deacetylase/ N-sulfotransferase family. The encoded enzyme is a type II transmembrane protein that resides in the Golgi apparatus. The encoded protein catalyzes the transfer of sulfate from 3'-phosphoadenosine 5'-phosphosulfate to nitrogen of glucosamine in heparan sulfate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":150485818,"end":150558211,"strand":1,"description":"N-deacetylase and N-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:7680]"}, {"versioned_ensembl_gene_id":"ENSG00000214389.2","gene_symbol":"RPS3AP26","gene_name":"ribosomal protein S3a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36513]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644972","summary":null,"start":98385801,"end":98386584,"strand":-1,"description":"ribosomal protein S3a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36513]"}, {"versioned_ensembl_gene_id":"ENSG00000255404.1","gene_symbol":"AP001266.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65795946,"end":65797219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237284.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29487242,"end":29488378,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000234948.1","gene_symbol":"LINC01524","gene_name":"long intergenic non-protein coding RNA 1524 [Source:HGNC Symbol;Acc:HGNC:51228]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927700","summary":null,"start":52210645,"end":52650431,"strand":1,"description":"long intergenic non-protein coding RNA 1524 [Source:HGNC Symbol;Acc:HGNC:51228]"}, {"versioned_ensembl_gene_id":"ENSG00000232465.1","gene_symbol":"AL049765.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52487922,"end":52500591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225785.1","gene_symbol":"AL109610.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52451464,"end":52455619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234821.1","gene_symbol":"MRPS33P4","gene_name":"mitochondrial ribosomal protein S33 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359777","summary":null,"start":52511252,"end":52511568,"strand":1,"description":"mitochondrial ribosomal protein S33 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29767]"}, {"versioned_ensembl_gene_id":"ENSG00000100578.14","gene_symbol":"KIAA0586","gene_name":"KIAA0586 [Source:HGNC Symbol;Acc:HGNC:19960]","synonyms":"Talpid3,JBTS23","biotype":"protein_coding","ncbi_id":"9786","summary":"This gene encodes a conserved centrosomal protein that functions in ciliogenesis and responds to hedgehog signaling. Mutations in this gene causes Joubert syndrome 23. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Aug 2016]","start":58427385,"end":58551289,"strand":1,"description":"KIAA0586 [Source:HGNC Symbol;Acc:HGNC:19960]"}, {"versioned_ensembl_gene_id":"ENSG00000235847.2","gene_symbol":"LDHAP7","gene_name":"lactate dehydrogenase A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23144]","synonyms":"LDHAL7","biotype":"processed_pseudogene","ncbi_id":"100190800","summary":null,"start":84777259,"end":84778223,"strand":-1,"description":"lactate dehydrogenase A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23144]"}, {"versioned_ensembl_gene_id":"ENSG00000258378.1","gene_symbol":"AL139021.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58398557,"end":58427125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219273.1","gene_symbol":"AL035555.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38762905,"end":38764694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163586.9","gene_symbol":"FABP1","gene_name":"fatty acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3555]","synonyms":"L-FABP","biotype":"protein_coding","ncbi_id":"2168","summary":"This gene encodes the fatty acid binding protein found in liver. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. This protein and FABP6 (the ileal fatty acid binding protein) are also able to bind bile acids. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism. [provided by RefSeq, Mar 2011]","start":88122982,"end":88128116,"strand":-1,"description":"fatty acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3555]"}, {"versioned_ensembl_gene_id":"ENSG00000104812.14","gene_symbol":"GYS1","gene_name":"glycogen synthase 1 [Source:HGNC Symbol;Acc:HGNC:4706]","synonyms":"GYS,GSY","biotype":"protein_coding","ncbi_id":"2997","summary":"The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":48968125,"end":48993310,"strand":-1,"description":"glycogen synthase 1 [Source:HGNC Symbol;Acc:HGNC:4706]"}, {"versioned_ensembl_gene_id":"ENSG00000259470.2","gene_symbol":"KRT8P9","gene_name":"keratin 8 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:33363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390601","summary":null,"start":70858714,"end":70860162,"strand":1,"description":"keratin 8 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:33363]"}, {"versioned_ensembl_gene_id":"ENSG00000260659.1","gene_symbol":"AC009113.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89226807,"end":89228692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254470.2","gene_symbol":"AP5B1","gene_name":"adaptor related protein complex 5 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:25104]","synonyms":"PP1030,DKFZp761E198,AP-5","biotype":"protein_coding","ncbi_id":"91056","summary":null,"start":65775893,"end":65780802,"strand":-1,"description":"adaptor related protein complex 5 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:25104]"}, {"versioned_ensembl_gene_id":"ENSG00000220113.2","gene_symbol":"MTCYBP4","gene_name":"mitochondrially encoded cytochrome b pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873169","summary":null,"start":133150568,"end":133150816,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:41923]"}, {"versioned_ensembl_gene_id":"ENSG00000259877.2","gene_symbol":"AC009113.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89215211,"end":89217653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282497.1","gene_symbol":"AC229888.9","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142634764,"end":142635309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231879.1","gene_symbol":"TXNL1P1","gene_name":"thioredoxin like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39459]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419095","summary":null,"start":86725500,"end":86726053,"strand":1,"description":"thioredoxin like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39459]"}, {"versioned_ensembl_gene_id":"ENSG00000214039.8","gene_symbol":"LINC02418","gene_name":"long intergenic non-protein coding RNA 2418 [Source:HGNC Symbol;Acc:HGNC:53348]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100190940","summary":null,"start":130033454,"end":130045057,"strand":-1,"description":"long intergenic non-protein coding RNA 2418 [Source:HGNC Symbol;Acc:HGNC:53348]"}, {"versioned_ensembl_gene_id":"ENSG00000232252.1","gene_symbol":"AL354994.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86060813,"end":86170890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283371.1","gene_symbol":"FO624990.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":86266842,"end":86266926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228241.1","gene_symbol":"MOB1AP1","gene_name":"MOB kinase activator 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42638]","synonyms":"MOBKL1BP1","biotype":"processed_pseudogene","ncbi_id":"100873874","summary":null,"start":85968999,"end":85969533,"strand":1,"description":"MOB kinase activator 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42638]"}, {"versioned_ensembl_gene_id":"ENSG00000229806.1","gene_symbol":"RPS15P5","gene_name":"ribosomal protein S15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35536]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729789","summary":null,"start":54626215,"end":54626646,"strand":1,"description":"ribosomal protein S15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35536]"}, {"versioned_ensembl_gene_id":"ENSG00000233176.3","gene_symbol":"OR7E157P","gene_name":"olfactory receptor family 7 subfamily E member 157 pseudogene [Source:HGNC Symbol;Acc:HGNC:31231]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403219","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7592006,"end":7592916,"strand":1,"description":"olfactory receptor family 7 subfamily E member 157 pseudogene [Source:HGNC Symbol;Acc:HGNC:31231]"}, {"versioned_ensembl_gene_id":"ENSG00000100575.13","gene_symbol":"TIMM9","gene_name":"translocase of inner mitochondrial membrane 9 [Source:HGNC Symbol;Acc:HGNC:11819]","synonyms":"TIM9A","biotype":"protein_coding","ncbi_id":"26520","summary":"TIMM9 belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004]","start":58408494,"end":58427614,"strand":-1,"description":"translocase of inner mitochondrial membrane 9 [Source:HGNC Symbol;Acc:HGNC:11819]"}, {"versioned_ensembl_gene_id":"ENSG00000258900.1","gene_symbol":"HNRNPCP1","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20017]","synonyms":"HNRPCP","biotype":"processed_pseudogene","ncbi_id":"319133","summary":null,"start":58521223,"end":58521988,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20017]"}, {"versioned_ensembl_gene_id":"ENSG00000138678.10","gene_symbol":"GPAT3","gene_name":"glycerol-3-phosphate acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:28157]","synonyms":"MGC11324,MAG1,LPAAT-theta,HMFN0839,AGPAT9,AGPAT10","biotype":"protein_coding","ncbi_id":"84803","summary":"This gene encodes a member of the lysophosphatidic acid acyltransferase protein family. The encoded protein is an enzyme which catalyzes the conversion of glycerol-3-phosphate to lysophosphatidic acid in the synthesis of triacylglycerol. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2012]","start":83535914,"end":83605875,"strand":1,"description":"glycerol-3-phosphate acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:28157]"}, {"versioned_ensembl_gene_id":"ENSG00000277725.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"cl-43,CD158B1,nkat6,CD158k","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754632,"end":54769000,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000115423.18","gene_symbol":"DNAH6","gene_name":"dynein axonemal heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:2951]","synonyms":"HL-2,FLJ37357,DNHL1,Dnahc6","biotype":"protein_coding","ncbi_id":"1768","summary":"This gene belongs to the dynein family, whose members encode large proteins that are constituents of the microtubule-associated motor protein complex. This complex is composed of dynein heavy, intermediate and light chains, which can be axonemal or cytoplasmic. This protein is an axonemal dynein heavy chain. It is involved in producing force for ciliary beating by using energy from ATP hydrolysis. Mutations in this gene may cause primary ciliary dyskinesia (PCD) as well as heterotaxy. [provided by RefSeq, Jun 2016]","start":84516455,"end":84819589,"strand":1,"description":"dynein axonemal heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:2951]"}, {"versioned_ensembl_gene_id":"ENSG00000282605.1","gene_symbol":"AC229888.10","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142622755,"end":142623265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244757.1","gene_symbol":"AL137024.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116288618,"end":116318689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266036.1","gene_symbol":"AC016888.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74747319,"end":74748912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160326.13","gene_symbol":"SLC2A6","gene_name":"solute carrier family 2 member 6 [Source:HGNC Symbol;Acc:HGNC:11011]","synonyms":"HSA011372,GLUT9,GLUT6","biotype":"protein_coding","ncbi_id":"11182","summary":"Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]","start":133471095,"end":133479137,"strand":-1,"description":"solute carrier family 2 member 6 [Source:HGNC Symbol;Acc:HGNC:11011]"}, {"versioned_ensembl_gene_id":"ENSG00000274162.1","gene_symbol":"SNX18P1Y","gene_name":"sorting nexin 18 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:38442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418999","summary":null,"start":11178306,"end":11178816,"strand":1,"description":"sorting nexin 18 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:38442]"}, {"versioned_ensembl_gene_id":"ENSG00000228735.1","gene_symbol":"AC011228.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54576052,"end":54578794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163479.13","gene_symbol":"SSR2","gene_name":"signal sequence receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:11324]","synonyms":"TRAPB,TLAP","biotype":"protein_coding","ncbi_id":"6746","summary":"The signal sequence receptor (SSR) is a glycosylated endoplasmic reticulum (ER) membrane receptor associated with protein translocation across the ER membrane. The SSR consists of 2 subunits, a 34-kD glycoprotein (alpha-SSR or SSR1) and a 22-kD glycoprotein (beta-SSR or SSR2). The human beta-signal sequence receptor gene (SSR2) maps to chromosome bands 1q21-q23. [provided by RefSeq, Jul 2008]","start":156009048,"end":156020959,"strand":-1,"description":"signal sequence receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:11324]"}, {"versioned_ensembl_gene_id":"ENSG00000235527.6","gene_symbol":"HIPK1-AS1","gene_name":"HIPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50576]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928846","summary":null,"start":113924000,"end":113929492,"strand":-1,"description":"HIPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50576]"}, {"versioned_ensembl_gene_id":"ENSG00000283782.1","gene_symbol":"AC116366.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":132410832,"end":132646079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262094.1","gene_symbol":"AC139099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83220527,"end":83227721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242407.1","gene_symbol":"AC091179.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48733091,"end":48733888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169432.14","gene_symbol":"SCN9A","gene_name":"sodium voltage-gated channel alpha subunit 9 [Source:HGNC Symbol;Acc:HGNC:10597]","synonyms":"PN1,NENA,NE-NA,Nav1.7,ETHA","biotype":"protein_coding","ncbi_id":"6335","summary":"This gene encodes a voltage-gated sodium channel which plays a significant role in nociception signaling. Mutations in this gene have been associated with primary erythermalgia, channelopathy-associated insensitivity to pain, and paroxysmal extreme pain disorder. [provided by RefSeq, Aug 2009]","start":166195185,"end":166375993,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 9 [Source:HGNC Symbol;Acc:HGNC:10597]"}, {"versioned_ensembl_gene_id":"ENSG00000232564.3","gene_symbol":"AL031594.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40521800,"end":40526707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261888.1","gene_symbol":"AC144831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83104255,"end":83106910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265713.1","gene_symbol":"AC023389.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":29775747,"end":29776701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265739.1","gene_symbol":"AC104984.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30122429,"end":30126118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234106.3","gene_symbol":"AP004242.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93535468,"end":93535816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124721.17","gene_symbol":"DNAH8","gene_name":"dynein axonemal heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]","synonyms":"hdhc9","biotype":"protein_coding","ncbi_id":"1769","summary":"The protein encoded by this gene is a heavy chain of an axonemal dynein involved in sperm and respiratory cilia motility. Axonemal dyneins generate force through hydrolysis of ATP and binding to microtubules. [provided by RefSeq, Jan 2012]","start":38715341,"end":39030529,"strand":1,"description":"dynein axonemal heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]"}, {"versioned_ensembl_gene_id":"ENSG00000182352.8","gene_symbol":"C17orf77","gene_name":"chromosome 17 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:26480]","synonyms":"FLJ31882","biotype":"antisense_RNA","ncbi_id":"146723","summary":null,"start":74584679,"end":74594209,"strand":1,"description":"chromosome 17 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:26480]"}, {"versioned_ensembl_gene_id":"ENSG00000253916.1","gene_symbol":"MTCO1P49","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:52114]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075177","summary":null,"start":133755845,"end":133756646,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:52114]"}, {"versioned_ensembl_gene_id":"ENSG00000261220.2","gene_symbol":"AC103706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133573183,"end":133573861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253970.1","gene_symbol":"MTND2P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873179","summary":null,"start":133754811,"end":133755450,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42141]"}, {"versioned_ensembl_gene_id":"ENSG00000178789.8","gene_symbol":"CD300LB","gene_name":"CD300 molecule like family member b [Source:HGNC Symbol;Acc:HGNC:30811]","synonyms":"TREM5,CLM7","biotype":"protein_coding","ncbi_id":"124599","summary":"CD300LB is a nonclassical activating receptor of the immunoglobulin (Ig) superfamily expressed on myeloid cells (Martinez-Barriocanal and Sayos, 2006 [PubMed 16920917]).[supplied by OMIM, Mar 2008]","start":74521174,"end":74531474,"strand":-1,"description":"CD300 molecule like family member b [Source:HGNC Symbol;Acc:HGNC:30811]"}, {"versioned_ensembl_gene_id":"ENSG00000068305.17","gene_symbol":"MEF2A","gene_name":"myocyte enhancer factor 2A [Source:HGNC Symbol;Acc:HGNC:6993]","synonyms":"RSRFC9,RSRFC4","biotype":"protein_coding","ncbi_id":"4205","summary":"The protein encoded by this gene is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]","start":99565417,"end":99716466,"strand":1,"description":"myocyte enhancer factor 2A [Source:HGNC Symbol;Acc:HGNC:6993]"}, {"versioned_ensembl_gene_id":"ENSG00000215906.8","gene_symbol":"LACTBL1","gene_name":"lactamase beta like 1 [Source:HGNC Symbol;Acc:HGNC:35445]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646262","summary":null,"start":22953043,"end":22965338,"strand":-1,"description":"lactamase beta like 1 [Source:HGNC Symbol;Acc:HGNC:35445]"}, {"versioned_ensembl_gene_id":"ENSG00000226111.8","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"HSPC183,PTD017,C6orf14,MRPS18-2","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30662345,"end":30671031,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000226776.1","gene_symbol":"KRTAP3-4P","gene_name":"keratin associated protein 3-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18919]","synonyms":"KRTAP3P1,KAP3A","biotype":"unprocessed_pseudogene","ncbi_id":"85345","summary":null,"start":41004481,"end":41004760,"strand":-1,"description":"keratin associated protein 3-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18919]"}, {"versioned_ensembl_gene_id":"ENSG00000167851.13","gene_symbol":"CD300A","gene_name":"CD300a molecule [Source:HGNC Symbol;Acc:HGNC:19319]","synonyms":"IGSF12,CMRF35H,CMRF-35-H9,Irp60,IRC2,IRC1","biotype":"protein_coding","ncbi_id":"11314","summary":"This gene encodes a member of the CD300 glycoprotein family of cell surface proteins found on leukocytes involved in immune response signaling pathways. This gene is located on chromosome 17 in a cluster with all but one of the other family members. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":74466416,"end":74484796,"strand":1,"description":"CD300a molecule [Source:HGNC Symbol;Acc:HGNC:19319]"}, {"versioned_ensembl_gene_id":"ENSG00000212900.2","gene_symbol":"KRTAP3-2","gene_name":"keratin associated protein 3-2 [Source:HGNC Symbol;Acc:HGNC:16779]","synonyms":"KAP3.2","biotype":"protein_coding","ncbi_id":"83897","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":40999193,"end":40999894,"strand":-1,"description":"keratin associated protein 3-2 [Source:HGNC Symbol;Acc:HGNC:16779]"}, {"versioned_ensembl_gene_id":"ENSG00000227366.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29926431,"end":29926616,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000251602.6","gene_symbol":"AL928654.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105416884,"end":105419739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258302.2","gene_symbol":"AC025034.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89561129,"end":89594878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232146.2","gene_symbol":"BX005432.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29291595,"end":29292537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254339.5","gene_symbol":"AC064802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114282067,"end":114295839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260757.1","gene_symbol":"AC093520.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":31402565,"end":31404699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242983.1","gene_symbol":"CABYRP1","gene_name":"calcium binding tyrosine phosphorylation regulated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31902]","synonyms":"CABYRP","biotype":"processed_pseudogene","ncbi_id":"266954","summary":null,"start":54047749,"end":54048793,"strand":-1,"description":"calcium binding tyrosine phosphorylation regulated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31902]"}, {"versioned_ensembl_gene_id":"ENSG00000269125.1","gene_symbol":"AL137002.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113165002,"end":113165183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186710.11","gene_symbol":"CFAP73","gene_name":"cilia and flagella associated protein 73 [Source:HGNC Symbol;Acc:HGNC:37100]","synonyms":"MIA2,CCDC42B","biotype":"protein_coding","ncbi_id":"387885","summary":null,"start":113149858,"end":113159276,"strand":1,"description":"cilia and flagella associated protein 73 [Source:HGNC Symbol;Acc:HGNC:37100]"}, {"versioned_ensembl_gene_id":"ENSG00000270415.1","gene_symbol":"DPPA3P3","gene_name":"developmental pluripotency associated 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481963","summary":null,"start":81114866,"end":81115295,"strand":-1,"description":"developmental pluripotency associated 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49062]"}, {"versioned_ensembl_gene_id":"ENSG00000258074.1","gene_symbol":"VTI1BP3","gene_name":"vesicle transport through interaction with t-SNAREs 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43729]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127976","summary":null,"start":53131350,"end":53131985,"strand":1,"description":"vesicle transport through interaction with t-SNAREs 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43729]"}, {"versioned_ensembl_gene_id":"ENSG00000265136.1","gene_symbol":"AC124283.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82576616,"end":82577391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277749.1","gene_symbol":"AC023300.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74311516,"end":74319688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198217.4","gene_symbol":"OR51H2P","gene_name":"olfactory receptor family 51 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15199]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401664","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4871717,"end":4878117,"strand":1,"description":"olfactory receptor family 51 subfamily H member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15199]"}, {"versioned_ensembl_gene_id":"ENSG00000242834.1","gene_symbol":"RPL7AP56","gene_name":"ribosomal protein L7a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35585]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271536","summary":null,"start":37725666,"end":37726456,"strand":1,"description":"ribosomal protein L7a pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35585]"}, {"versioned_ensembl_gene_id":"ENSG00000156886.11","gene_symbol":"ITGAD","gene_name":"integrin subunit alpha D [Source:HGNC Symbol;Acc:HGNC:6146]","synonyms":"CD11d,ADB2","biotype":"protein_coding","ncbi_id":"3681","summary":"This gene belongs to the beta-2 integrin family of membrane glycoproteins, which are are composed of non-covalently linked alpha and beta subunits to form a heterodimer. It encodes the alpha subunit of the cell surface heterodimers and is involved in the activation and adhesion functions of leukocytes. The gene is located about 11kb downstream of the integrin subunit alpha X gene, another member of the integrin family. It is expressed in the tissue and circulating myeloid leukocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":31393312,"end":31426505,"strand":1,"description":"integrin subunit alpha D [Source:HGNC Symbol;Acc:HGNC:6146]"}, {"versioned_ensembl_gene_id":"ENSG00000204969.6","gene_symbol":"PCDHA2","gene_name":"protocadherin alpha 2 [Source:HGNC Symbol;Acc:HGNC:8668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56146","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140794852,"end":141012344,"strand":1,"description":"protocadherin alpha 2 [Source:HGNC Symbol;Acc:HGNC:8668]"}, {"versioned_ensembl_gene_id":"ENSG00000152763.16","gene_symbol":"WDR78","gene_name":"WD repeat domain 78 [Source:HGNC Symbol;Acc:HGNC:26252]","synonyms":"FLJ23129,DIC4","biotype":"protein_coding","ncbi_id":"79819","summary":null,"start":66812885,"end":66924887,"strand":-1,"description":"WD repeat domain 78 [Source:HGNC Symbol;Acc:HGNC:26252]"}, {"versioned_ensembl_gene_id":"ENSG00000231080.1","gene_symbol":"AL592161.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66826942,"end":66828558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261835.1","gene_symbol":"AC007610.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50046496,"end":50047798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279726.1","gene_symbol":"AC005609.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140788457,"end":140822193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279356.1","gene_symbol":"AC007610.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50072862,"end":50074986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276551.1","gene_symbol":"AC008746.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54387840,"end":54388311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121039.9","gene_symbol":"RDH10","gene_name":"retinol dehydrogenase 10 [Source:HGNC Symbol;Acc:HGNC:19975]","synonyms":"SDR16C4","biotype":"protein_coding","ncbi_id":"157506","summary":"This gene encodes a retinol dehydrogenase, which converts all-trans-retinol to all-trans-retinal, with preference for NADP as a cofactor. Studies in mice suggest that this protein is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development. [provided by RefSeq, Dec 2011]","start":73294612,"end":73325281,"strand":1,"description":"retinol dehydrogenase 10 [Source:HGNC Symbol;Acc:HGNC:19975]"}, {"versioned_ensembl_gene_id":"ENSG00000167978.16","gene_symbol":"SRRM2","gene_name":"serine/arginine repetitive matrix 2 [Source:HGNC Symbol;Acc:HGNC:16639]","synonyms":"KIAA0324,Cwc21,SRm300,SRL300","biotype":"protein_coding","ncbi_id":"23524","summary":null,"start":2752329,"end":2772538,"strand":1,"description":"serine/arginine repetitive matrix 2 [Source:HGNC Symbol;Acc:HGNC:16639]"}, {"versioned_ensembl_gene_id":"ENSG00000104412.7","gene_symbol":"EMC2","gene_name":"ER membrane protein complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28963]","synonyms":"TTC35,KIAA0103","biotype":"protein_coding","ncbi_id":"9694","summary":null,"start":108443601,"end":108486918,"strand":1,"description":"ER membrane protein complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28963]"}, {"versioned_ensembl_gene_id":"ENSG00000233230.1","gene_symbol":"AC079807.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47905678,"end":47907810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282040.1","gene_symbol":"AC233282.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142553725,"end":142554208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213752.3","gene_symbol":"AL008718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45275599,"end":45276085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235193.1","gene_symbol":"AC006987.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10088026,"end":10089586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274726.4","gene_symbol":"ARHGEF10","gene_name":"Rho guanine nucleotide exchange factor 10 [Source:HGNC Symbol;Acc:HGNC:14103]","synonyms":"KIAA0294,Gef10","biotype":"protein_coding","ncbi_id":"9639","summary":"This gene encodes a Rho guanine nucleotide exchange factor (GEF). Rho GEFs regulate the activity of small Rho GTPases by stimulating the exchange of guanine diphosphate (GDP) for guanine triphosphate (GTP) and may play a role in neural morphogenesis. Mutations in this gene are associated with slowed nerve conduction velocity (SNCV). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":1823976,"end":1958641,"strand":1,"description":"Rho guanine nucleotide exchange factor 10 [Source:HGNC Symbol;Acc:HGNC:14103]"}, {"versioned_ensembl_gene_id":"ENSG00000105767.2","gene_symbol":"CADM4","gene_name":"cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:30825]","synonyms":"TSLL2,SynCAM4,Necl-4,IGSF4C","biotype":"protein_coding","ncbi_id":"199731","summary":null,"start":43622368,"end":43639839,"strand":-1,"description":"cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:30825]"}, {"versioned_ensembl_gene_id":"ENSG00000242978.1","gene_symbol":"AC004534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144434826,"end":144435314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134107.4","gene_symbol":"BHLHE40","gene_name":"basic helix-loop-helix family member e40 [Source:HGNC Symbol;Acc:HGNC:1046]","synonyms":"STRA13,SHARP2,DEC1,Clast5,bHLHe40,BHLHB2","biotype":"protein_coding","ncbi_id":"8553","summary":"This gene encodes a basic helix-loop-helix protein expressed in various tissues. The encoded protein can interact with ARNTL or compete for E-box binding sites in the promoter of PER1 and repress CLOCK/ARNTL's transactivation of PER1. This gene is believed to be involved in the control of circadian rhythm and cell differentiation. [provided by RefSeq, Feb 2014]","start":4979116,"end":4985323,"strand":1,"description":"basic helix-loop-helix family member e40 [Source:HGNC Symbol;Acc:HGNC:1046]"}, {"versioned_ensembl_gene_id":"ENSG00000225183.1","gene_symbol":"AL353898.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54089856,"end":54090093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248106.2","gene_symbol":"AC116353.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140764110,"end":140764821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281327.1","gene_symbol":"LINC01338","gene_name":"long intergenic non-protein coding RNA 1338 [Source:HGNC Symbol;Acc:HGNC:50547]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546175","summary":null,"start":82850864,"end":82859836,"strand":-1,"description":"long intergenic non-protein coding RNA 1338 [Source:HGNC Symbol;Acc:HGNC:50547]"}, {"versioned_ensembl_gene_id":"ENSG00000142698.14","gene_symbol":"C1orf94","gene_name":"chromosome 1 open reading frame 94 [Source:HGNC Symbol;Acc:HGNC:28250]","synonyms":"MGC15882","biotype":"protein_coding","ncbi_id":"84970","summary":null,"start":34166883,"end":34219131,"strand":1,"description":"chromosome 1 open reading frame 94 [Source:HGNC Symbol;Acc:HGNC:28250]"}, {"versioned_ensembl_gene_id":"ENSG00000279269.1","gene_symbol":"AP003072.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93206990,"end":93207583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284188.1","gene_symbol":"AL451007.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":244730375,"end":244730962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167332.8","gene_symbol":"OR51E2","gene_name":"olfactory receptor family 51 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:15195]","synonyms":"PSGR","biotype":"protein_coding","ncbi_id":"81285","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4680171,"end":4697854,"strand":-1,"description":"olfactory receptor family 51 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:15195]"}, {"versioned_ensembl_gene_id":"ENSG00000250505.1","gene_symbol":"AC006499.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10284961,"end":10285708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224462.2","gene_symbol":"C4BPAP1","gene_name":"complement component 4 binding protein, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1326]","synonyms":"C4BPAL1","biotype":"unprocessed_pseudogene","ncbi_id":"727859","summary":null,"start":207165496,"end":207183910,"strand":1,"description":"complement component 4 binding protein, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1326]"}, {"versioned_ensembl_gene_id":"ENSG00000248192.1","gene_symbol":"ATG10-AS1","gene_name":"ATG10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40914]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874022","summary":null,"start":82073055,"end":82073702,"strand":-1,"description":"ATG10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40914]"}, {"versioned_ensembl_gene_id":"ENSG00000269692.1","gene_symbol":"FKBP4P2","gene_name":"FK506 binding protein 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389727","summary":null,"start":39631046,"end":39632416,"strand":1,"description":"FK506 binding protein 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50371]"}, {"versioned_ensembl_gene_id":"ENSG00000239207.2","gene_symbol":"GAPDHP39","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37796]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128589","summary":null,"start":138777832,"end":138778810,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37796]"}, {"versioned_ensembl_gene_id":"ENSG00000229175.1","gene_symbol":"LINC00382","gene_name":"long intergenic non-protein coding RNA 382 [Source:HGNC Symbol;Acc:HGNC:42709]","synonyms":"TCONS_00021500","biotype":"lincRNA","ncbi_id":"101927195","summary":null,"start":79872586,"end":79917944,"strand":1,"description":"long intergenic non-protein coding RNA 382 [Source:HGNC Symbol;Acc:HGNC:42709]"}, {"versioned_ensembl_gene_id":"ENSG00000106268.15","gene_symbol":"NUDT1","gene_name":"nudix hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:8048]","synonyms":"MTH1","biotype":"protein_coding","ncbi_id":"4521","summary":"Misincorporation of oxidized nucleoside triphosphates into DNA/RNA during replication and transcription can cause mutations that may result in carcinogenesis or neurodegeneration. The protein encoded by this gene is an enzyme that hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP, 8-oxo-dATP, 2-hydroxy-dATP, and 2-hydroxy rATP, to monophosphates, thereby preventing misincorporation. The encoded protein is localized mainly in the cytoplasm, with some in the mitochondria, suggesting that it is involved in the sanitization of nucleotide pools both for nuclear and mitochondrial genomes. Several alternatively spliced transcript variants, some of which encode distinct isoforms, have been identified. Additional variants have been observed, but their full-length natures have not been determined. A rare single-nucleotide polymorphism that results in the production of an additional, longer isoform (p26) has been described. [provided by RefSeq, Dec 2018]","start":2242222,"end":2251146,"strand":1,"description":"nudix hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:8048]"}, {"versioned_ensembl_gene_id":"ENSG00000237707.1","gene_symbol":"AL031726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169104124,"end":169104907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104408.9","gene_symbol":"EIF3E","gene_name":"eukaryotic translation initiation factor 3 subunit E [Source:HGNC Symbol;Acc:HGNC:3277]","synonyms":"INT6,EIF3S6,eIF3e,eIF3-p48","biotype":"protein_coding","ncbi_id":"3646","summary":null,"start":108201216,"end":108435333,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit E [Source:HGNC Symbol;Acc:HGNC:3277]"}, {"versioned_ensembl_gene_id":"ENSG00000224038.1","gene_symbol":"BX005214.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39384506,"end":39405305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175548.8","gene_symbol":"ALG10B","gene_name":"ALG10B, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:31088]","synonyms":"KCR1","biotype":"protein_coding","ncbi_id":"144245","summary":null,"start":38316578,"end":38329728,"strand":1,"description":"ALG10B, alpha-1,2-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:31088]"}, {"versioned_ensembl_gene_id":"ENSG00000230234.1","gene_symbol":"AL162582.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160272617,"end":160276130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215367.10","gene_symbol":"TMED11P","gene_name":"transmembrane p24 trafficking protein 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:35401]","synonyms":"p24alpha1,p24a1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100379220","summary":null,"start":1115197,"end":1153726,"strand":-1,"description":"transmembrane p24 trafficking protein 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:35401]"}, {"versioned_ensembl_gene_id":"ENSG00000234308.2","gene_symbol":"LINC01878","gene_name":"long intergenic non-protein coding RNA 1878 [Source:HGNC Symbol;Acc:HGNC:52697]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102725079","summary":null,"start":212795331,"end":212819264,"strand":1,"description":"long intergenic non-protein coding RNA 1878 [Source:HGNC Symbol;Acc:HGNC:52697]"}, {"versioned_ensembl_gene_id":"ENSG00000165948.10","gene_symbol":"IFI27L1","gene_name":"interferon alpha inducible protein 27 like 1 [Source:HGNC Symbol;Acc:HGNC:19754]","synonyms":"FAM14B","biotype":"protein_coding","ncbi_id":"122509","summary":null,"start":94081282,"end":94103846,"strand":1,"description":"interferon alpha inducible protein 27 like 1 [Source:HGNC Symbol;Acc:HGNC:19754]"}, {"versioned_ensembl_gene_id":"ENSG00000219930.4","gene_symbol":"GAPDHP67","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:4145]","synonyms":"GAPDL12,GAPDHL12","biotype":"processed_pseudogene","ncbi_id":"2609","summary":null,"start":136077844,"end":136078631,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:4145]"}, {"versioned_ensembl_gene_id":"ENSG00000180257.13","gene_symbol":"ZNF816","gene_name":"zinc finger protein 816 [Source:HGNC Symbol;Acc:HGNC:26995]","synonyms":"ZNF816A","biotype":"protein_coding","ncbi_id":"125893","summary":null,"start":52949379,"end":52962911,"strand":-1,"description":"zinc finger protein 816 [Source:HGNC Symbol;Acc:HGNC:26995]"}, {"versioned_ensembl_gene_id":"ENSG00000272254.1","gene_symbol":"AC022893.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73042910,"end":73043346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269082.1","gene_symbol":"AC010328.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52956041,"end":52981654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256986.2","gene_symbol":"AC140847.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34162477,"end":34163442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277750.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803572,"end":54814476,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000136237.18","gene_symbol":"RAPGEF5","gene_name":"Rap guanine nucleotide exchange factor 5 [Source:HGNC Symbol;Acc:HGNC:16862]","synonyms":"KIAA0277,GFR,MR-GEF","biotype":"protein_coding","ncbi_id":"9771","summary":"Members of the RAS (see HRAS; MIM 190020) subfamily of GTPases function in signal transduction as GTP/GDP-regulated switches that cycle between inactive GDP- and active GTP-bound states. Guanine nucleotide exchange factors (GEFs), such as RAPGEF5, serve as RAS activators by promoting acquisition of GTP to maintain the active GTP-bound state and are the key link between cell surface receptors and RAS activation (Rebhun et al., 2000 [PubMed 10934204]).[supplied by OMIM, Mar 2008]","start":22118238,"end":22357144,"strand":-1,"description":"Rap guanine nucleotide exchange factor 5 [Source:HGNC Symbol;Acc:HGNC:16862]"}, {"versioned_ensembl_gene_id":"ENSG00000278635.1","gene_symbol":"AC141557.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9415641,"end":9416718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213889.10","gene_symbol":"PPM1N","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1N (putative) [Source:HGNC Symbol;Acc:HGNC:26845]","synonyms":"FLJ40125","biotype":"protein_coding","ncbi_id":"147699","summary":null,"start":45488777,"end":45502510,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1N (putative) [Source:HGNC Symbol;Acc:HGNC:26845]"}, {"versioned_ensembl_gene_id":"ENSG00000258480.1","gene_symbol":"AL352977.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40387558,"end":40389140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071994.10","gene_symbol":"PDCD2","gene_name":"programmed cell death 2 [Source:HGNC Symbol;Acc:HGNC:8762]","synonyms":"ZMYND7,RP8","biotype":"protein_coding","ncbi_id":"5134","summary":"This gene encodes a nuclear protein expressed in a variety of tissues. Expression of this gene has been shown to be repressed by B-cell CLL/lymphoma 6 (BCL6), a transcriptional repressor required for lymph node germinal center development, suggesting that BCL6 regulates apoptosis by its effects on this protein. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 9 and 12. [provided by RefSeq, Dec 2010]","start":170575295,"end":170584692,"strand":-1,"description":"programmed cell death 2 [Source:HGNC Symbol;Acc:HGNC:8762]"}, {"versioned_ensembl_gene_id":"ENSG00000229028.2","gene_symbol":"KRT223P","gene_name":"keratin 223 pseudogene [Source:HGNC Symbol;Acc:HGNC:32968]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643115","summary":null,"start":40717235,"end":40721932,"strand":-1,"description":"keratin 223 pseudogene [Source:HGNC Symbol;Acc:HGNC:32968]"}, {"versioned_ensembl_gene_id":"ENSG00000230975.1","gene_symbol":"AC012355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80699388,"end":80870190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255628.1","gene_symbol":"AC140847.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34149839,"end":34162238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254347.1","gene_symbol":"AC011131.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72462311,"end":72470972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232702.3","gene_symbol":"AL158050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51410081,"end":51410537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212989.3","gene_symbol":"AC124293.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72429620,"end":72430112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271250.1","gene_symbol":"AL158032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21216555,"end":21216660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144028.14","gene_symbol":"SNRNP200","gene_name":"small nuclear ribonucleoprotein U5 subunit 200 [Source:HGNC Symbol;Acc:HGNC:30859]","synonyms":"U5-200KD,RP33,KIAA0788,HELIC2,BRR2,ASCC3L1","biotype":"protein_coding","ncbi_id":"23020","summary":"Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010]","start":96274336,"end":96305515,"strand":-1,"description":"small nuclear ribonucleoprotein U5 subunit 200 [Source:HGNC Symbol;Acc:HGNC:30859]"}, {"versioned_ensembl_gene_id":"ENSG00000143184.4","gene_symbol":"XCL1","gene_name":"X-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10645]","synonyms":"LTN,LPTN,ATAC,SCYC1,SCM-1a,SCM-1","biotype":"protein_coding","ncbi_id":"6375","summary":"This antimicrobial gene encodes a member of the chemokine superfamily. Chemokines function in inflammatory and immunological responses, inducing leukocyte migration and activation. The encoded protein is a member of the C-chemokine subfamily, retaining only two of four cysteines conserved in other chemokines, and is thought to be specifically chemotactic for T cells. This gene and a closely related family member are located on the long arm of chromosome 1. [provided by RefSeq, Sep 2014]","start":168576473,"end":168582077,"strand":1,"description":"X-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10645]"}, {"versioned_ensembl_gene_id":"ENSG00000267461.1","gene_symbol":"AC079210.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68557516,"end":68582577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234876.5","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32202513,"end":32231740,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000240963.1","gene_symbol":"AL645465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":244375100,"end":244409592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255070.1","gene_symbol":"OSBPL9P3","gene_name":"oxysterol binding protein like 9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48733]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420591","summary":null,"start":91115961,"end":91116555,"strand":1,"description":"oxysterol binding protein like 9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48733]"}, {"versioned_ensembl_gene_id":"ENSG00000095397.13","gene_symbol":"WHRN","gene_name":"whirlin [Source:HGNC Symbol;Acc:HGNC:16361]","synonyms":"USH2D,PDZD7B,DFNB31,CIP98","biotype":"protein_coding","ncbi_id":"25861","summary":"This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":114402080,"end":114505450,"strand":-1,"description":"whirlin [Source:HGNC Symbol;Acc:HGNC:16361]"}, {"versioned_ensembl_gene_id":"ENSG00000271214.1","gene_symbol":"AL138895.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114491564,"end":114491741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143185.3","gene_symbol":"XCL2","gene_name":"X-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:10646]","synonyms":"SCYC2,SCM-1b","biotype":"protein_coding","ncbi_id":"6846","summary":null,"start":168540765,"end":168543997,"strand":-1,"description":"X-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:10646]"}, {"versioned_ensembl_gene_id":"ENSG00000205433.4","gene_symbol":"SNRPGP6","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39325]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861574","summary":null,"start":116409256,"end":116409475,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39325]"}, {"versioned_ensembl_gene_id":"ENSG00000237854.3","gene_symbol":"LINC00674","gene_name":"long intergenic non-protein coding RNA 674 [Source:HGNC Symbol;Acc:HGNC:44355]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100499466","summary":null,"start":68101908,"end":68115518,"strand":1,"description":"long intergenic non-protein coding RNA 674 [Source:HGNC Symbol;Acc:HGNC:44355]"}, {"versioned_ensembl_gene_id":"ENSG00000264472.4","gene_symbol":"AC096708.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68899781,"end":68902255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266010.1","gene_symbol":"GATA6-AS1","gene_name":"GATA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48840]","synonyms":"locus5689,BM742401","biotype":"lincRNA","ncbi_id":"100128893","summary":null,"start":22166898,"end":22168968,"strand":-1,"description":"GATA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48840]"}, {"versioned_ensembl_gene_id":"ENSG00000159348.12","gene_symbol":"CYB5R1","gene_name":"cytochrome b5 reductase 1 [Source:HGNC Symbol;Acc:HGNC:13397]","synonyms":"NQO3A2,humb5R2","biotype":"protein_coding","ncbi_id":"51706","summary":null,"start":202961869,"end":202967280,"strand":-1,"description":"cytochrome b5 reductase 1 [Source:HGNC Symbol;Acc:HGNC:13397]"}, {"versioned_ensembl_gene_id":"ENSG00000239523.5","gene_symbol":"MYLK-AS1","gene_name":"MYLK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42440]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506826","summary":null,"start":123585542,"end":123644568,"strand":1,"description":"MYLK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42440]"}, {"versioned_ensembl_gene_id":"ENSG00000264149.1","gene_symbol":"AC103987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21871446,"end":21893996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183506.17","gene_symbol":"PI4KAP2","gene_name":"phosphatidylinositol 4-kinase alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33577]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375133","summary":null,"start":21473000,"end":21517533,"strand":-1,"description":"phosphatidylinositol 4-kinase alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33577]"}, {"versioned_ensembl_gene_id":"ENSG00000256321.5","gene_symbol":"AC087258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23099368,"end":23191587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115934.11","gene_symbol":"AC087235.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23181334,"end":23251499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258526.5","gene_symbol":"AL049875.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39474840,"end":39513780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108175.16","gene_symbol":"ZMIZ1","gene_name":"zinc finger MIZ-type containing 1 [Source:HGNC Symbol;Acc:HGNC:16493]","synonyms":"RAI17,MIZ,KIAA1224,hZIMP10,FLJ13541,Zimp10,RP11-519K18.1","biotype":"protein_coding","ncbi_id":"57178","summary":"This gene encodes a member of the PIAS (protein inhibitor of activated STAT) family of proteins. The encoded protein regulates the activity of various transcription factors, including the androgen receptor, Smad3/4, and p53. The encoded protein may also play a role in sumoylation. A translocation between this locus on chromosome 10 and the protein tyrosine kinase ABL1 locus on chromosome 9 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Mar 2010]","start":79069035,"end":79316528,"strand":1,"description":"zinc finger MIZ-type containing 1 [Source:HGNC Symbol;Acc:HGNC:16493]"}, {"versioned_ensembl_gene_id":"ENSG00000225932.3","gene_symbol":"CTAGE4","gene_name":"CTAGE family member 4 [Source:HGNC Symbol;Acc:HGNC:24772]","synonyms":"FLJ43692,cTAGE-4","biotype":"protein_coding","ncbi_id":"100128553","summary":null,"start":144183466,"end":144186053,"strand":1,"description":"CTAGE family member 4 [Source:HGNC Symbol;Acc:HGNC:24772]"}, {"versioned_ensembl_gene_id":"ENSG00000135577.4","gene_symbol":"NMBR","gene_name":"neuromedin B receptor [Source:HGNC Symbol;Acc:HGNC:7843]","synonyms":"BB1,BB1R","biotype":"protein_coding","ncbi_id":"4829","summary":"This gene encodes a 7-transmembrane G protein-coupled receptor that binds neuromedin B, which is a growth factor and mitogen for gastrointestinal epithelial tissue and for normal and neoplastic lung. This receptor may play a role in smooth muscle contraction, neuronal responses, and the regulation of cell growth. Antagonists of this receptor have a potential therapeutic use in inhibiting tumor cell growth. Polymorphisms in this gene may be associated with a susceptibility for schizophrenia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":142058330,"end":142088799,"strand":-1,"description":"neuromedin B receptor [Source:HGNC Symbol;Acc:HGNC:7843]"}, {"versioned_ensembl_gene_id":"ENSG00000239981.1","gene_symbol":"OR2A15P","gene_name":"olfactory receptor family 2 subfamily A member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15085]","synonyms":"OR2A28P","biotype":"unprocessed_pseudogene","ncbi_id":"135942","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144118461,"end":144119360,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:15085]"}, {"versioned_ensembl_gene_id":"ENSG00000221989.2","gene_symbol":"OR2A2","gene_name":"olfactory receptor family 2 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8230]","synonyms":"OST008,OR2A2P,OR2A17P","biotype":"protein_coding","ncbi_id":"442361","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144109514,"end":144110564,"strand":1,"description":"olfactory receptor family 2 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8230]"}, {"versioned_ensembl_gene_id":"ENSG00000247131.5","gene_symbol":"AC025263.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69713633,"end":69738568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258199.1","gene_symbol":"AC073896.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":56162359,"end":56190284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106948.16","gene_symbol":"AKNA","gene_name":"AT-hook transcription factor [Source:HGNC Symbol;Acc:HGNC:24108]","synonyms":"KIAA1968","biotype":"protein_coding","ncbi_id":"80709","summary":null,"start":114334156,"end":114394405,"strand":-1,"description":"AT-hook transcription factor [Source:HGNC Symbol;Acc:HGNC:24108]"}, {"versioned_ensembl_gene_id":"ENSG00000196636.7","gene_symbol":"SDHAF3","gene_name":"succinate dehydrogenase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:21752]","synonyms":"LYRM10,DC11,ACN9,Sdh7","biotype":"protein_coding","ncbi_id":"57001","summary":null,"start":97116590,"end":97181763,"strand":1,"description":"succinate dehydrogenase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:21752]"}, {"versioned_ensembl_gene_id":"ENSG00000161692.17","gene_symbol":"DBF4B","gene_name":"DBF4 zinc finger B [Source:HGNC Symbol;Acc:HGNC:17883]","synonyms":"ZDBF1B,FLJ13087,DRF1,chifb,ASKL1","biotype":"protein_coding","ncbi_id":"80174","summary":"This gene encodes a regulator of the cell division cycle 7 homolog (S. cerevisiae) protein, a serine-threonine kinase which links cell cycle regulation to genome duplication. This protein localizes to the nucleus and, in complex with the cell division cycle 7 homolog (S. cerevisiae) protein, may facilitate M phase progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":44708608,"end":44752264,"strand":1,"description":"DBF4 zinc finger B [Source:HGNC Symbol;Acc:HGNC:17883]"}, {"versioned_ensembl_gene_id":"ENSG00000186881.3","gene_symbol":"OR13F1","gene_name":"olfactory receptor family 13 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:14723]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138805","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104504263,"end":104505222,"strand":1,"description":"olfactory receptor family 13 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:14723]"}, {"versioned_ensembl_gene_id":"ENSG00000203396.3","gene_symbol":"AL512646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104328320,"end":104329396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266472.5","gene_symbol":"MRPS21","gene_name":"mitochondrial ribosomal protein S21 [Source:HGNC Symbol;Acc:HGNC:14046]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54460","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S21P family. Pseudogenes corresponding to this gene are found on chromosomes 1p, 1q, 9p, 10p, 10q, 16q, and 17q. Available sequence data analyses identified splice variants that differ in the 5' UTR; both transcripts encode the same protein. [provided by RefSeq, Jul 2008]","start":150293720,"end":150308979,"strand":1,"description":"mitochondrial ribosomal protein S21 [Source:HGNC Symbol;Acc:HGNC:14046]"}, {"versioned_ensembl_gene_id":"ENSG00000249219.1","gene_symbol":"AC108199.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9922814,"end":9924146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253552.7","gene_symbol":"HOXA-AS2","gene_name":"HOXA cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43745]","synonyms":"HOXA3as","biotype":"antisense_RNA","ncbi_id":"285943","summary":"This gene produces a long non-coding RNA that promotes cell proliferation. This transcript may interact with enhancer of zeste homolog 2 Polycomb repressive complex to repress gene expression. [provided by RefSeq, Dec 2017]","start":27107777,"end":27134302,"strand":1,"description":"HOXA cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43745]"}, {"versioned_ensembl_gene_id":"ENSG00000134853.11","gene_symbol":"PDGFRA","gene_name":"platelet derived growth factor receptor alpha [Source:HGNC Symbol;Acc:HGNC:8803]","synonyms":"PDGFR2,GAS9,CD140a","biotype":"protein_coding","ncbi_id":"5156","summary":"This gene encodes a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. Studies suggest that this gene plays a role in organ development, wound healing, and tumor progression. Mutations in this gene have been associated with idiopathic hypereosinophilic syndrome, somatic and familial gastrointestinal stromal tumors, and a variety of other cancers. [provided by RefSeq, Mar 2012]","start":54229097,"end":54298247,"strand":1,"description":"platelet derived growth factor receptor alpha [Source:HGNC Symbol;Acc:HGNC:8803]"}, {"versioned_ensembl_gene_id":"ENSG00000256633.1","gene_symbol":"AP005019.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72584572,"end":72587979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253743.1","gene_symbol":"MARK2P11","gene_name":"microtubule affinity regulating kinase 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421484","summary":null,"start":157984658,"end":157989990,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39802]"}, {"versioned_ensembl_gene_id":"ENSG00000165943.4","gene_symbol":"MOAP1","gene_name":"modulator of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:16658]","synonyms":"PNMA4,MAP-1","biotype":"protein_coding","ncbi_id":"64112","summary":"The protein encoded by this gene was identified by its interaction with apoptosis regulator BAX protein. This protein contains a Bcl-2 homology 3 (BH3)-like motif, which is required for the association with BAX. When overexpressed, this gene has been shown to mediate caspase-dependent apoptosis. [provided by RefSeq, Jul 2008]","start":93182196,"end":93184928,"strand":-1,"description":"modulator of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:16658]"}, {"versioned_ensembl_gene_id":"ENSG00000264057.1","gene_symbol":"AC103810.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64927634,"end":64934203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234705.1","gene_symbol":"HMGA1P4","gene_name":"high mobility group AT-hook 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39093]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506080","summary":null,"start":128663134,"end":128663578,"strand":-1,"description":"high mobility group AT-hook 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39093]"}, {"versioned_ensembl_gene_id":"ENSG00000259079.1","gene_symbol":"AC005476.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71330342,"end":71330738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257122.5","gene_symbol":"RRN3P3","gene_name":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37620]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100131998","summary":null,"start":22418672,"end":22437715,"strand":-1,"description":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37620]"}, {"versioned_ensembl_gene_id":"ENSG00000230395.1","gene_symbol":"AC092651.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87118534,"end":87120980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204936.9","gene_symbol":"CD177","gene_name":"CD177 molecule [Source:HGNC Symbol;Acc:HGNC:30072]","synonyms":"NB1,HNA2A,PRV1","biotype":"protein_coding","ncbi_id":"57126","summary":"This gene encodes a glycosyl-phosphatidylinositol (GPI)-linked cell surface glycoprotein that plays a role in neutrophil activation. The protein can bind platelet endothelial cell adhesion molecule-1 and function in neutrophil transmigration. Mutations in this gene are associated with myeloproliferative diseases. Over-expression of this gene has been found in patients with polycythemia rubra vera. Autoantibodies against the protein may result in pulmonary transfusion reactions, and it may be involved in Wegener's granulomatosis. A related pseudogene, which is adjacent to this gene on chromosome 19, has been identified. [provided by RefSeq, Apr 2014]","start":43353659,"end":43363172,"strand":1,"description":"CD177 molecule [Source:HGNC Symbol;Acc:HGNC:30072]"}, {"versioned_ensembl_gene_id":"ENSG00000256069.7","gene_symbol":"A2MP1","gene_name":"alpha-2-macroglobulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8]","synonyms":"A2MP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3","summary":null,"start":9228533,"end":9275817,"strand":-1,"description":"alpha-2-macroglobulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8]"}, {"versioned_ensembl_gene_id":"ENSG00000265478.2","gene_symbol":"AC107982.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18809956,"end":18810940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258998.1","gene_symbol":"LINC02302","gene_name":"long intergenic non-protein coding RNA 2302 [Source:HGNC Symbol;Acc:HGNC:53221]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927351","summary":null,"start":44763157,"end":44782829,"strand":-1,"description":"long intergenic non-protein coding RNA 2302 [Source:HGNC Symbol;Acc:HGNC:53221]"}, {"versioned_ensembl_gene_id":"ENSG00000189139.5","gene_symbol":"FSCB","gene_name":"fibrous sheath CABYR binding protein [Source:HGNC Symbol;Acc:HGNC:20494]","synonyms":"DKFZP434F1017,C14orf155","biotype":"protein_coding","ncbi_id":"84075","summary":null,"start":44504342,"end":44507279,"strand":-1,"description":"fibrous sheath CABYR binding protein [Source:HGNC Symbol;Acc:HGNC:20494]"}, {"versioned_ensembl_gene_id":"ENSG00000140105.17","gene_symbol":"WARS","gene_name":"tryptophanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12729]","synonyms":"IFI53,IFP53","biotype":"protein_coding","ncbi_id":"7453","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Two forms of tryptophanyl-tRNA synthetase exist, a cytoplasmic form, named WARS, and a mitochondrial form, named WARS2. Tryptophanyl-tRNA synthetase (WARS) catalyzes the aminoacylation of tRNA(trp) with tryptophan and is induced by interferon. Tryptophanyl-tRNA synthetase belongs to the class I tRNA synthetase family. Four transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":100333788,"end":100376805,"strand":-1,"description":"tryptophanyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12729]"}, {"versioned_ensembl_gene_id":"ENSG00000257035.1","gene_symbol":"AC025252.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127624153,"end":127626267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258581.2","gene_symbol":"AL157871.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100366628,"end":100366920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165370.1","gene_symbol":"GPR101","gene_name":"G protein-coupled receptor 101 [Source:HGNC Symbol;Acc:HGNC:14963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83550","summary":"The protein encoded by this gene is an orphan G protein-coupled receptor of unknown function. The encoded protein is a member of a family of proteins that contain seven transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. [provided by RefSeq, Sep 2011]","start":137030148,"end":137031674,"strand":-1,"description":"G protein-coupled receptor 101 [Source:HGNC Symbol;Acc:HGNC:14963]"}, {"versioned_ensembl_gene_id":"ENSG00000075340.22","gene_symbol":"ADD2","gene_name":"adducin 2 [Source:HGNC Symbol;Acc:HGNC:244]","synonyms":"ADDB","biotype":"protein_coding","ncbi_id":"119","summary":"Adducins are heteromeric proteins composed of different subunits referred to as adducin alpha, beta and gamma. The three subunits are encoded by distinct genes and belong to a family of membrane skeletal proteins involved in the assembly of spectrin-actin network in erythrocytes and at sites of cell-cell contact in epithelial tissues. While adducins alpha and gamma are ubiquitously expressed, the expression of adducin beta is restricted to brain and hematopoietic tissues. Adducin, originally purified from human erythrocytes, was found to be a heterodimer of adducins alpha and beta. Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension. Heterodimers consisting of alpha and gamma subunits have also been described. Structurally, each subunit is comprised of two distinct domains. The amino-terminal region is protease resistant and globular in shape, while the carboxy-terminal region is protease sensitive. The latter contains multiple phosphorylation sites for protein kinase C, the binding site for calmodulin, and is required for association with spectrin and actin. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2010]","start":70607618,"end":70768225,"strand":-1,"description":"adducin 2 [Source:HGNC Symbol;Acc:HGNC:244]"}, {"versioned_ensembl_gene_id":"ENSG00000273454.1","gene_symbol":"AC112503.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123277353,"end":123277904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251105.1","gene_symbol":"AC110792.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54076625,"end":54076848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278396.1","gene_symbol":"AL122023.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93334528,"end":93335057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234921.1","gene_symbol":"AC006450.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124031624,"end":124032524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100605.16","gene_symbol":"ITPK1","gene_name":"inositol-tetrakisphosphate 1-kinase [Source:HGNC Symbol;Acc:HGNC:6177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3705","summary":"This gene encodes an enzyme that belongs to the inositol 1,3,4-trisphosphate 5/6-kinase family. This enzyme regulates the synthesis of inositol tetraphosphate, and downstream products, inositol pentakisphosphate and inositol hexakisphosphate. Inositol metabolism plays a role in the development of the neural tube. Disruptions in this gene are thought to be associated with neural tube defects. A pseudogene of this gene has been identified on chromosome X. [provided by RefSeq, Jul 2016]","start":92936914,"end":93116320,"strand":-1,"description":"inositol-tetrakisphosphate 1-kinase [Source:HGNC Symbol;Acc:HGNC:6177]"}, {"versioned_ensembl_gene_id":"ENSG00000179331.2","gene_symbol":"RAB39A","gene_name":"RAB39A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16521]","synonyms":"RAB39","biotype":"protein_coding","ncbi_id":"54734","summary":null,"start":107928503,"end":107963482,"strand":1,"description":"RAB39A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16521]"}, {"versioned_ensembl_gene_id":"ENSG00000237109.1","gene_symbol":"RPL21P111","gene_name":"ribosomal protein L21 pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:36564]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271439","summary":null,"start":78761175,"end":78761651,"strand":1,"description":"ribosomal protein L21 pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:36564]"}, {"versioned_ensembl_gene_id":"ENSG00000236046.1","gene_symbol":"AC004920.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50839363,"end":50841992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181929.11","gene_symbol":"PRKAG1","gene_name":"protein kinase AMP-activated non-catalytic subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:9385]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5571","summary":"The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit is one of the gamma regulatory subunits of AMPK. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":49002274,"end":49019197,"strand":-1,"description":"protein kinase AMP-activated non-catalytic subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:9385]"}, {"versioned_ensembl_gene_id":"ENSG00000101898.5","gene_symbol":"MCTS2P","gene_name":"malignant T-cell amplified sequence 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49760]","synonyms":"psiMCT-1,MCTS2","biotype":"processed_pseudogene","ncbi_id":"100101490","summary":"This locus represents a retrogene copy of MCTS1 (GeneID:28985) and contains an ORF similar to that parent gene. This retrogene might not be transcribed independently of the overlapping HM13 gene (GeneID:81502), and therefore, this locus is currently represented as a pseudogene. This locus is situated in a differentially methylated region (DMR) and transcripts in this region are imprinted. [provided by RefSeq, Nov 2015]","start":31547504,"end":31548049,"strand":1,"description":"malignant T-cell amplified sequence 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49760]"}, {"versioned_ensembl_gene_id":"ENSG00000275448.1","gene_symbol":"AC027506.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64677796,"end":64677993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255340.1","gene_symbol":"AC087276.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43378882,"end":43385671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248869.5","gene_symbol":"LINC02511","gene_name":"long intergenic non-protein coding RNA 2511 [Source:HGNC Symbol;Acc:HGNC:53500]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377441","summary":null,"start":136796722,"end":137212799,"strand":-1,"description":"long intergenic non-protein coding RNA 2511 [Source:HGNC Symbol;Acc:HGNC:53500]"}, {"versioned_ensembl_gene_id":"ENSG00000086589.11","gene_symbol":"RBM22","gene_name":"RNA binding motif protein 22 [Source:HGNC Symbol;Acc:HGNC:25503]","synonyms":"ZC3H16,fSAP47,FLJ10290,Cwc2","biotype":"protein_coding","ncbi_id":"55696","summary":"This gene encodes an RNA binding protein. The encoded protein may play a role in cell division and may be involved in pre-mRNA splicing. Related pseudogenes exist on chromosomes 6, 7, 9, 13, 16, 18, and X. [provided by RefSeq, Mar 2009]","start":150690794,"end":150701107,"strand":-1,"description":"RNA binding motif protein 22 [Source:HGNC Symbol;Acc:HGNC:25503]"}, {"versioned_ensembl_gene_id":"ENSG00000271746.1","gene_symbol":"AL031848.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6393555,"end":6394391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256362.1","gene_symbol":"LINC02375","gene_name":"long intergenic non-protein coding RNA 2375 [Source:HGNC Symbol;Acc:HGNC:53297]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927616","summary":null,"start":127324155,"end":127340072,"strand":-1,"description":"long intergenic non-protein coding RNA 2375 [Source:HGNC Symbol;Acc:HGNC:53297]"}, {"versioned_ensembl_gene_id":"ENSG00000254641.1","gene_symbol":"AC091564.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":6608667,"end":6610135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250665.1","gene_symbol":"AC073429.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136125909,"end":136138874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274584.1","gene_symbol":"AP001282.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106824025,"end":106824954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260583.1","gene_symbol":"AP000223.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25582770,"end":25583326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100731.15","gene_symbol":"PCNX1","gene_name":"pecanex homolog 1 [Source:HGNC Symbol;Acc:HGNC:19740]","synonyms":"KIAA0805,pecanex,PCNXL1,PCNX,KIAA0995","biotype":"protein_coding","ncbi_id":"22990","summary":"This gene encodes an evolutionarily conserved transmembrane protein similar to the pecanex protein in Drosophila. The fly protein is a component of the Notch signaling pathway, which functions in several developmental processes. [provided by RefSeq, Jul 2016]","start":70907405,"end":71115382,"strand":1,"description":"pecanex homolog 1 [Source:HGNC Symbol;Acc:HGNC:19740]"}, {"versioned_ensembl_gene_id":"ENSG00000258969.1","gene_symbol":"LINC02307","gene_name":"long intergenic non-protein coding RNA 2307 [Source:HGNC Symbol;Acc:HGNC:53226]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370471","summary":null,"start":43995781,"end":44384545,"strand":-1,"description":"long intergenic non-protein coding RNA 2307 [Source:HGNC Symbol;Acc:HGNC:53226]"}, {"versioned_ensembl_gene_id":"ENSG00000032444.15","gene_symbol":"PNPLA6","gene_name":"patatin like phospholipase domain containing 6 [Source:HGNC Symbol;Acc:HGNC:16268]","synonyms":"sws,SPG39,NTE,iPLA2delta","biotype":"protein_coding","ncbi_id":"10908","summary":"This gene encodes a phospholipase that deacetylates intracellular phosphatidylcholine to produce glycerophosphocholine. It is thought to function in neurite outgrowth and process elongation during neuronal differentiation. The protein is anchored to the cytoplasmic face of the endoplasmic reticulum in both neurons and non-neuronal cells. Mutations in this gene result in autosomal recessive spastic paraplegia, and the protein is the target for neurodegeneration induced by organophosphorus compounds and chemical warfare agents. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":7534004,"end":7561764,"strand":1,"description":"patatin like phospholipase domain containing 6 [Source:HGNC Symbol;Acc:HGNC:16268]"}, {"versioned_ensembl_gene_id":"ENSG00000259977.1","gene_symbol":"AL121578.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37906147,"end":37949405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090674.15","gene_symbol":"MCOLN1","gene_name":"mucolipin 1 [Source:HGNC Symbol;Acc:HGNC:13356]","synonyms":"TRPML1,TRPM-L1,MSTP080,MST080,MLIV,ML4","biotype":"protein_coding","ncbi_id":"57192","summary":"This gene encodes a memberof the transient receptor potential (TRP) cation channel gene family. The transmembrane protein localizes to intracellular vesicular membranes including lysosomes, and functions in the late endocytic pathway and in the regulation of lysosomal exocytosis. The channel is permeable to Ca(2+), Fe(2+), Na(+), K(+), and H(+), and is modulated by changes in Ca(2+) concentration. Mutations in this gene result in mucolipidosis type IV. [provided by RefSeq, Oct 2009]","start":7522626,"end":7534009,"strand":1,"description":"mucolipin 1 [Source:HGNC Symbol;Acc:HGNC:13356]"}, {"versioned_ensembl_gene_id":"ENSG00000168769.13","gene_symbol":"TET2","gene_name":"tet methylcytosine dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:25941]","synonyms":"KIAA1546,FLJ20032","biotype":"protein_coding","ncbi_id":"54790","summary":"The protein encoded by this gene is a methylcytosine dioxygenase that catalyzes the conversion of methylcytosine to 5-hydroxymethylcytosine. The encoded protein is involved in myelopoiesis, and defects in this gene have been associated with several myeloproliferative disorders. Two variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":105145875,"end":105279816,"strand":1,"description":"tet methylcytosine dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:25941]"}, {"versioned_ensembl_gene_id":"ENSG00000255650.5","gene_symbol":"FAM222A-AS1","gene_name":"FAM222A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28223]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"84983","summary":null,"start":109734166,"end":109773508,"strand":-1,"description":"FAM222A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28223]"}, {"versioned_ensembl_gene_id":"ENSG00000170522.9","gene_symbol":"ELOVL6","gene_name":"ELOVL fatty acid elongase 6 [Source:HGNC Symbol;Acc:HGNC:15829]","synonyms":"MGC5487,LCE,FLJ23378","biotype":"protein_coding","ncbi_id":"79071","summary":"Fatty acid elongases (EC 6.2.1.3), such as ELOVL6, use malonyl-CoA as a 2-carbon donor in the first and rate-limiting step of fatty acid elongation (Moon et al., 2001 [PubMed 11567032]).[supplied by OMIM, Mar 2008]","start":110045846,"end":110199199,"strand":-1,"description":"ELOVL fatty acid elongase 6 [Source:HGNC Symbol;Acc:HGNC:15829]"}, {"versioned_ensembl_gene_id":"ENSG00000281453.1","gene_symbol":"TGFB2-OT1","gene_name":"TGFB2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50629]","synonyms":"FLJ11812","biotype":"3prime_overlapping_ncRNA","ncbi_id":"103611157","summary":null,"start":218442626,"end":218443996,"strand":1,"description":"TGFB2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:50629]"}, {"versioned_ensembl_gene_id":"ENSG00000163050.16","gene_symbol":"COQ8A","gene_name":"coenzyme Q8A [Source:HGNC Symbol;Acc:HGNC:16812]","synonyms":"SCAR9,COQ8,CABC1,ADCK3","biotype":"protein_coding","ncbi_id":"56997","summary":"This gene encodes a mitochondrial protein similar to yeast ABC1, which functions in an electron-transferring membrane protein complex in the respiratory chain. It is not related to the family of ABC transporter proteins. Expression of this gene is induced by the tumor suppressor p53 and in response to DNA damage, and inhibiting its expression partially suppresses p53-induced apoptosis. Alternatively spliced transcript variants have been found; however, their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":226897536,"end":226987545,"strand":1,"description":"coenzyme Q8A [Source:HGNC Symbol;Acc:HGNC:16812]"}, {"versioned_ensembl_gene_id":"ENSG00000147036.11","gene_symbol":"LANCL3","gene_name":"LanC like 3 [Source:HGNC Symbol;Acc:HGNC:24767]","synonyms":"FLJ42925","biotype":"protein_coding","ncbi_id":"347404","summary":null,"start":37571569,"end":37684463,"strand":1,"description":"LanC like 3 [Source:HGNC Symbol;Acc:HGNC:24767]"}, {"versioned_ensembl_gene_id":"ENSG00000029993.14","gene_symbol":"HMGB3","gene_name":"high mobility group box 3 [Source:HGNC Symbol;Acc:HGNC:5004]","synonyms":"HMG4,HMG2A,MGC90319","biotype":"protein_coding","ncbi_id":"3149","summary":"This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":150980509,"end":150990775,"strand":1,"description":"high mobility group box 3 [Source:HGNC Symbol;Acc:HGNC:5004]"}, {"versioned_ensembl_gene_id":"ENSG00000229146.2","gene_symbol":"SNX18P4","gene_name":"sorting nexin 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418976","summary":null,"start":66082350,"end":66083187,"strand":-1,"description":"sorting nexin 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39612]"}, {"versioned_ensembl_gene_id":"ENSG00000228525.1","gene_symbol":"AL353689.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226958069,"end":226958267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275130.1","gene_symbol":"AL592227.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11618496,"end":11618621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226030.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32730758,"end":32731695,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000259863.1","gene_symbol":"SH3RF3-AS1","gene_name":"SH3RF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44168]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287216","summary":null,"start":109127327,"end":109128930,"strand":-1,"description":"SH3RF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44168]"}, {"versioned_ensembl_gene_id":"ENSG00000248950.1","gene_symbol":"LDHBP3","gene_name":"lactate dehydrogenase B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39136]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129283","summary":null,"start":92840807,"end":92841628,"strand":-1,"description":"lactate dehydrogenase B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39136]"}, {"versioned_ensembl_gene_id":"ENSG00000161551.14","gene_symbol":"ZNF577","gene_name":"zinc finger protein 577 [Source:HGNC Symbol;Acc:HGNC:28673]","synonyms":"MGC4400","biotype":"protein_coding","ncbi_id":"84765","summary":null,"start":51804816,"end":51890950,"strand":-1,"description":"zinc finger protein 577 [Source:HGNC Symbol;Acc:HGNC:28673]"}, {"versioned_ensembl_gene_id":"ENSG00000145012.13","gene_symbol":"LPP","gene_name":"LIM domain containing preferred translocation partner in lipoma [Source:HGNC Symbol;Acc:HGNC:6679]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4026","summary":"This gene encodes a member of a subfamily of LIM domain proteins that are characterized by an N-terminal proline-rich region and three C-terminal LIM domains. The encoded protein localizes to the cell periphery in focal adhesions and may be involved in cell-cell adhesion and cell motility. This protein also shuttles through the nucleus and may function as a transcriptional co-activator. This gene is located at the junction of certain disease-related chromosomal translocations, which result in the expression of chimeric proteins that may promote tumor growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":188153284,"end":188890671,"strand":1,"description":"LIM domain containing preferred translocation partner in lipoma [Source:HGNC Symbol;Acc:HGNC:6679]"}, {"versioned_ensembl_gene_id":"ENSG00000230714.1","gene_symbol":"AL355526.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":218031835,"end":218033660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282711.1","gene_symbol":"TRBV11-1","gene_name":"T-cell receptor beta variable 11-1 [Source:HGNC Symbol;Acc:HGNC:12180]","synonyms":"TRBV111,TCRBV21S1,TCRBV11S1","biotype":"TR_V_gene","ncbi_id":"28582","summary":null,"start":142429379,"end":142429843,"strand":1,"description":"T-cell receptor beta variable 11-1 [Source:HGNC Symbol;Acc:HGNC:12180]"}, {"versioned_ensembl_gene_id":"ENSG00000249345.6","gene_symbol":"LINC02405","gene_name":"long intergenic non-protein coding RNA 2405 [Source:HGNC Symbol;Acc:HGNC:53333]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927592","summary":null,"start":126915203,"end":127060401,"strand":-1,"description":"long intergenic non-protein coding RNA 2405 [Source:HGNC Symbol;Acc:HGNC:53333]"}, {"versioned_ensembl_gene_id":"ENSG00000256817.1","gene_symbol":"TPT1P12","gene_name":"tumor protein, translationally-controlled 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49303]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421480","summary":null,"start":9155881,"end":9156372,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49303]"}, {"versioned_ensembl_gene_id":"ENSG00000234680.1","gene_symbol":"VN2R3P","gene_name":"vomeronasal 2 receptor 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33209]","synonyms":"VN2R8P,VN2R5P,VN2R4P","biotype":"unitary_pseudogene","ncbi_id":"100033392","summary":null,"start":39016969,"end":39039594,"strand":1,"description":"vomeronasal 2 receptor 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:33209]"}, {"versioned_ensembl_gene_id":"ENSG00000239216.1","gene_symbol":"AL139420.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119000618,"end":119001405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233871.2","gene_symbol":"DLG5-AS1","gene_name":"DLG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45109]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100128292","summary":null,"start":77927372,"end":77929824,"strand":1,"description":"DLG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45109]"}, {"versioned_ensembl_gene_id":"ENSG00000227200.1","gene_symbol":"AL162724.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":124262876,"end":124265809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235204.1","gene_symbol":"AL162724.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124259250,"end":124261156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174791.10","gene_symbol":"RIN1","gene_name":"Ras and Rab interactor 1 [Source:HGNC Symbol;Acc:HGNC:18749]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9610","summary":null,"start":66330242,"end":66336840,"strand":-1,"description":"Ras and Rab interactor 1 [Source:HGNC Symbol;Acc:HGNC:18749]"}, {"versioned_ensembl_gene_id":"ENSG00000156313.12","gene_symbol":"RPGR","gene_name":"retinitis pigmentosa GTPase regulator [Source:HGNC Symbol;Acc:HGNC:10295]","synonyms":"RP15,CRD,CORDX1,COD1,RP3","biotype":"protein_coding","ncbi_id":"6103","summary":"This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008]","start":38269163,"end":38327564,"strand":-1,"description":"retinitis pigmentosa GTPase regulator [Source:HGNC Symbol;Acc:HGNC:10295]"}, {"versioned_ensembl_gene_id":"ENSG00000225919.1","gene_symbol":"LINC01745","gene_name":"long intergenic non-protein coding RNA 1745 [Source:HGNC Symbol;Acc:HGNC:52533]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373199","summary":null,"start":232718071,"end":232722250,"strand":1,"description":"long intergenic non-protein coding RNA 1745 [Source:HGNC Symbol;Acc:HGNC:52533]"}, {"versioned_ensembl_gene_id":"ENSG00000248682.1","gene_symbol":"ARHGAP22-IT1","gene_name":"ARHGAP22 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42944]","synonyms":"FLJ35752","biotype":"sense_intronic","ncbi_id":"100689073","summary":null,"start":48510525,"end":48511589,"strand":-1,"description":"ARHGAP22 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42944]"}, {"versioned_ensembl_gene_id":"ENSG00000224290.7","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31639825,"end":31645618,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000274286.1","gene_symbol":"ADRA2B","gene_name":"adrenoceptor alpha 2B [Source:HGNC Symbol;Acc:HGNC:282]","synonyms":"ADRARL1,ADRA2RL1,ADRA2L1","biotype":"protein_coding","ncbi_id":"151","summary":"This intronless gene encodes a seven-pass transmembrane protein. This protein is a member of a subfamily of G protein-coupled receptors that regulate neurotransmitter release from sympathetic nerves and from adrenergic neurons in the central nervous system. [provided by RefSeq, Apr 2014]","start":96112875,"end":96116245,"strand":-1,"description":"adrenoceptor alpha 2B [Source:HGNC Symbol;Acc:HGNC:282]"}, {"versioned_ensembl_gene_id":"ENSG00000104490.17","gene_symbol":"NCALD","gene_name":"neurocalcin delta [Source:HGNC Symbol;Acc:HGNC:7655]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83988","summary":"This gene encodes a member of the neuronal calcium sensor (NCS) family of calcium-binding proteins. The protein contains an N-terminal myristoylation signal and four EF-hand calcium binding loops. The protein is cytosolic at resting calcium levels; however, elevated intracellular calcium levels induce a conformational change that exposes the myristoyl group, resulting in protein association with membranes and partial co-localization with the perinuclear trans-golgi network. The protein is thought to be a regulator of G protein-coupled receptor signal transduction. Several alternatively spliced variants of this gene have been determined, all of which encode the same protein; additional variants may exist but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":101686543,"end":102124907,"strand":-1,"description":"neurocalcin delta [Source:HGNC Symbol;Acc:HGNC:7655]"}, {"versioned_ensembl_gene_id":"ENSG00000282785.1","gene_symbol":"AC140479.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110279606,"end":110285681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000019995.6","gene_symbol":"ZRANB1","gene_name":"zinc finger RANBP2-type containing 1 [Source:HGNC Symbol;Acc:HGNC:18224]","synonyms":"TRABID","biotype":"protein_coding","ncbi_id":"54764","summary":null,"start":124942123,"end":124988189,"strand":1,"description":"zinc finger RANBP2-type containing 1 [Source:HGNC Symbol;Acc:HGNC:18224]"}, {"versioned_ensembl_gene_id":"ENSG00000282989.1","gene_symbol":"AP001206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101871830,"end":101872549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258501.1","gene_symbol":"EIF3LP1","gene_name":"eukaryotic translation initiation factor 3 subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20010]","synonyms":"EIF3S6IPP,EIF3EIPP1","biotype":"processed_pseudogene","ncbi_id":"319117","summary":null,"start":81916231,"end":81917888,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20010]"}, {"versioned_ensembl_gene_id":"ENSG00000164117.13","gene_symbol":"FBXO8","gene_name":"F-box protein 8 [Source:HGNC Symbol;Acc:HGNC:13587]","synonyms":"FBX8,FBS","biotype":"protein_coding","ncbi_id":"26269","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. It contains a C-terminal amino acid sequence that bears a significant similarity with a portion of yeast Sec7p, a critical regulator of vesicular protein transport. This human protein may interact with ADP-ribosylation factor(s)(ARFs) and exhibit ARF-GEF (guanine nucleotide exchange factor) activity. [provided by RefSeq, Jul 2008]","start":174236658,"end":174284264,"strand":-1,"description":"F-box protein 8 [Source:HGNC Symbol;Acc:HGNC:13587]"}, {"versioned_ensembl_gene_id":"ENSG00000250812.2","gene_symbol":"AC021220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55219344,"end":55219973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277552.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724203,"end":54736221,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000249472.1","gene_symbol":"AC147055.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68614419,"end":68615013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280244.1","gene_symbol":"AL512356.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":105110347,"end":105110807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251213.1","gene_symbol":"AC012055.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174164441,"end":174168913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277203.1","gene_symbol":"F8A1","gene_name":"coagulation factor VIII associated 1 [Source:HGNC Symbol;Acc:HGNC:3547]","synonyms":"F8A,DXS522E","biotype":"protein_coding","ncbi_id":"8263","summary":"This gene is contained entirely within intron 22 of the factor VIII gene; spans less than 2 kb, and is transcribed in the direction opposite of factor VIII. A portion of intron 22 (int22h), containing F8A, is repeated twice extragenically closer to the Xq telomere. Although its function is unknown, the observation that this gene is conserved in the mouse implies it has some function. Unlike factor VIII, this gene is transcribed abundantly in a wide variety of cell types. [provided by RefSeq, Jul 2008]","start":154886349,"end":154888061,"strand":1,"description":"coagulation factor VIII associated 1 [Source:HGNC Symbol;Acc:HGNC:3547]"}, {"versioned_ensembl_gene_id":"ENSG00000160813.6","gene_symbol":"PPP1R35","gene_name":"protein phosphatase 1 regulatory subunit 35 [Source:HGNC Symbol;Acc:HGNC:28320]","synonyms":"MGC22793,C7orf47","biotype":"protein_coding","ncbi_id":"221908","summary":null,"start":100435282,"end":100436565,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 35 [Source:HGNC Symbol;Acc:HGNC:28320]"}, {"versioned_ensembl_gene_id":"ENSG00000240211.1","gene_symbol":"AC092849.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100436204,"end":100438504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282897.1","gene_symbol":"AL162727.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":113614589,"end":113617375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232707.1","gene_symbol":"AP1B1P2","gene_name":"adaptor related protein complex 1 beta 1 subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:298]","synonyms":"dJ127L4.3,ADTB1L2","biotype":"unprocessed_pseudogene","ncbi_id":"23781","summary":null,"start":32134028,"end":32134133,"strand":1,"description":"adaptor related protein complex 1 beta 1 subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:298]"}, {"versioned_ensembl_gene_id":"ENSG00000233817.1","gene_symbol":"AL162727.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113619228,"end":113622634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264186.1","gene_symbol":"SNRPCP4","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310848","summary":null,"start":2990652,"end":2991078,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49819]"}, {"versioned_ensembl_gene_id":"ENSG00000239674.2","gene_symbol":"Z83839.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32141267,"end":32143272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168779.19","gene_symbol":"SHOX2","gene_name":"short stature homeobox 2 [Source:HGNC Symbol;Acc:HGNC:10854]","synonyms":"SHOT,OG12X,OG12","biotype":"protein_coding","ncbi_id":"6474","summary":"This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":158095954,"end":158106503,"strand":-1,"description":"short stature homeobox 2 [Source:HGNC Symbol;Acc:HGNC:10854]"}, {"versioned_ensembl_gene_id":"ENSG00000262791.1","gene_symbol":"AC130343.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1725748,"end":1738585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230736.2","gene_symbol":"AL021937.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32376664,"end":32384343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180189.10","gene_symbol":"HMGB1P14","gene_name":"high mobility group box 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:20014]","synonyms":"HMGB1P,HMGB1L14","biotype":"processed_pseudogene","ncbi_id":"319130","summary":null,"start":58284773,"end":58285363,"strand":1,"description":"high mobility group box 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:20014]"}, {"versioned_ensembl_gene_id":"ENSG00000258519.1","gene_symbol":"AL121579.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58184576,"end":58185507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214642.1","gene_symbol":"DEFB113","gene_name":"defensin beta 113 [Source:HGNC Symbol;Acc:HGNC:18094]","synonyms":"DEFB-13","biotype":"protein_coding","ncbi_id":"245927","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":49968677,"end":49969625,"strand":-1,"description":"defensin beta 113 [Source:HGNC Symbol;Acc:HGNC:18094]"}, {"versioned_ensembl_gene_id":"ENSG00000237112.8","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"GPRC3A,hGB1a","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555562,"end":29633117,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000206288.13","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"KE4,D6S2244E,ZIP7,HKE4,RING5,H2-KE4","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33129256,"end":33133250,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000279157.1","gene_symbol":"AL162574.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":106941950,"end":106942561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251216.1","gene_symbol":"AC106895.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173924207,"end":173990861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268235.6","gene_symbol":"TCP11X1","gene_name":"t-complex 11 family, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:48369]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100996631","summary":null,"start":102215301,"end":102229532,"strand":1,"description":"t-complex 11 family, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:48369]"}, {"versioned_ensembl_gene_id":"ENSG00000258846.1","gene_symbol":"EEF1A1P33","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:37911]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390352","summary":null,"start":96900697,"end":96902698,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:37911]"}, {"versioned_ensembl_gene_id":"ENSG00000225426.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29528958,"end":29533106,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000250043.1","gene_symbol":"AC106895.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173877471,"end":173913252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280399.1","gene_symbol":"AC022497.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":138482065,"end":138485755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281237.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000277863.1","gene_symbol":"AL162574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106903150,"end":106904099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268530.5","gene_symbol":"AC008403.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48465593,"end":48469693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251571.1","gene_symbol":"DDX3P3","gene_name":"DEAD-box helicase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42173]","synonyms":"DDX3YP3","biotype":"processed_pseudogene","ncbi_id":"650560","summary":null,"start":103572089,"end":103574082,"strand":1,"description":"DEAD-box helicase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42173]"}, {"versioned_ensembl_gene_id":"ENSG00000267319.1","gene_symbol":"AC093227.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37693280,"end":37693564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267115.1","gene_symbol":"AC022148.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37503906,"end":37504465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228840.3","gene_symbol":"BX927133.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29488804,"end":29489209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225376.5","gene_symbol":"TMEM246-AS1","gene_name":"TMEM246 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51191]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928470","summary":null,"start":101468439,"end":101481502,"strand":1,"description":"TMEM246 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51191]"}, {"versioned_ensembl_gene_id":"ENSG00000078177.13","gene_symbol":"N4BP2","gene_name":"NEDD4 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29851]","synonyms":"B3BP","biotype":"protein_coding","ncbi_id":"55728","summary":"This gene encodes a protein containing a polynucleotide kinase domain (PNK) near the N-terminal region, and a Small MutS Related (Smr) domain near the C-terminal region. The encoded protein can bind to both B-cell leukemia/lymphoma 3 (BCL-3) and neural precursor cell expressed, developmentally downregulated 4, (Nedd4) proteins. This protein binds and hydrolyzes ATP, may function as a 5'-polynucleotide kinase, and has the capacity to be a ubiquitylation substrate. This protein may play a role in transcription-coupled DNA repair or genetic recombination. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":40056826,"end":40158252,"strand":1,"description":"NEDD4 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29851]"}, {"versioned_ensembl_gene_id":"ENSG00000248977.1","gene_symbol":"AC095057.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40142198,"end":40142365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196437.10","gene_symbol":"ZNF569","gene_name":"zinc finger protein 569 [Source:HGNC Symbol;Acc:HGNC:24737]","synonyms":"ZAP1,FLJ32053","biotype":"protein_coding","ncbi_id":"148266","summary":null,"start":37411155,"end":37469275,"strand":-1,"description":"zinc finger protein 569 [Source:HGNC Symbol;Acc:HGNC:24737]"}, {"versioned_ensembl_gene_id":"ENSG00000105866.13","gene_symbol":"SP4","gene_name":"Sp4 transcription factor [Source:HGNC Symbol;Acc:HGNC:11209]","synonyms":"SPR-1,MGC130009,MGC130008,HF1B","biotype":"protein_coding","ncbi_id":"6671","summary":"The protein encoded by this gene is a transcription factor that can bind to the GC promoter region of a variety of genes, including those of the photoreceptor signal transduction system. The encoded protein binds to the same sites in promoter CpG islands as does the transcription factor SP1, although its expression is much more restricted compared to that of SP1. This gene may be involved in bipolar disorder and schizophrenia. [provided by RefSeq, May 2016]","start":21428034,"end":21514822,"strand":1,"description":"Sp4 transcription factor [Source:HGNC Symbol;Acc:HGNC:11209]"}, {"versioned_ensembl_gene_id":"ENSG00000237439.1","gene_symbol":"Z83839.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32129689,"end":32130612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132780.16","gene_symbol":"NASP","gene_name":"nuclear autoantigenic sperm protein [Source:HGNC Symbol;Acc:HGNC:7644]","synonyms":"FLJ35510,FLJ31599,FLB7527,DKFZp547F162,PRO1999,MGC2297,MGC20372,MGC19722","biotype":"protein_coding","ncbi_id":"4678","summary":"This gene encodes a H1 histone binding protein that is involved in transporting histones into the nucleus of dividing cells. Multiple isoforms are encoded by transcript variants of this gene. The somatic form is expressed in all mitotic cells, is localized to the nucleus, and is coupled to the cell cycle. The testicular form is expressed in embryonic tissues, tumor cells, and the testis. In male germ cells, this protein is localized to the cytoplasm of primary spermatocytes, the nucleus of spermatids, and the periacrosomal region of mature spermatozoa. [provided by RefSeq, Jul 2008]","start":45583846,"end":45618904,"strand":1,"description":"nuclear autoantigenic sperm protein [Source:HGNC Symbol;Acc:HGNC:7644]"}, {"versioned_ensembl_gene_id":"ENSG00000231653.1","gene_symbol":"AC010731.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206640073,"end":206641282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214669.3","gene_symbol":"AL157702.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113758994,"end":113759419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232905.2","gene_symbol":"AL162393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113850687,"end":113851632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235118.7","gene_symbol":"FAM237A","gene_name":"family with sequence similarity 237 member A [Source:HGNC Symbol;Acc:HGNC:52388]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200726","summary":null,"start":206642418,"end":206649449,"strand":1,"description":"family with sequence similarity 237 member A [Source:HGNC Symbol;Acc:HGNC:52388]"}, {"versioned_ensembl_gene_id":"ENSG00000263606.1","gene_symbol":"AP000919.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":2945550,"end":2946890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254498.1","gene_symbol":"AC104042.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36696317,"end":36697867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254389.3","gene_symbol":"RHPN1-AS1","gene_name":"RHPN1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28457]","synonyms":"MGC3113,C8orf51","biotype":"antisense_RNA","ncbi_id":"78998","summary":null,"start":143366631,"end":143368548,"strand":-1,"description":"RHPN1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28457]"}, {"versioned_ensembl_gene_id":"ENSG00000163535.17","gene_symbol":"SGO2","gene_name":"shugoshin 2 [Source:HGNC Symbol;Acc:HGNC:30812]","synonyms":"TRIPIN,SGOL2,FLJ25211","biotype":"protein_coding","ncbi_id":"151246","summary":null,"start":200510008,"end":200583782,"strand":1,"description":"shugoshin 2 [Source:HGNC Symbol;Acc:HGNC:30812]"}, {"versioned_ensembl_gene_id":"ENSG00000250191.1","gene_symbol":"AC105252.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":133574566,"end":133575208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232125.2","gene_symbol":"DYTN","gene_name":"dystrotelin [Source:HGNC Symbol;Acc:HGNC:23279]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391475","summary":"This gene belongs to the dystrophin superfamily, which is characterized by the presence of four EF-hand motifs and a ZZ-domain. It is a likely ortholog of the Drosophila 'discontinuous actin hexagon' gene. It is noteworthy that the coding region of this gene lacks two coding exons that are found in the mouse ortholog. Human transcripts including these two exons are subject to nonsense-mediated transcript decay (NMD). On the other hand, transcripts skipping the two coding exons are expressed at very low levels. While this gene maintains an intact CDS, it may be an evolving pseudogene. However, after a discussion about this gene within the RefSeq group, as well as in the consensus coding sequence (CCDS) collaboration, it was decided to keep it as a protein-coding gene in the RefSeq, Ensembl-GENCODE and the CCDS sets. [provided by RefSeq, Jul 2019]","start":206651621,"end":206718396,"strand":-1,"description":"dystrotelin [Source:HGNC Symbol;Acc:HGNC:23279]"}, {"versioned_ensembl_gene_id":"ENSG00000265907.1","gene_symbol":"AP000919.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2948238,"end":2960756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140009.18","gene_symbol":"ESR2","gene_name":"estrogen receptor 2 [Source:HGNC Symbol;Acc:HGNC:3468]","synonyms":"NR3A2,Erb","biotype":"protein_coding","ncbi_id":"2100","summary":"This gene encodes a member of the family of estrogen receptors and superfamily of nuclear receptor transcription factors. The gene product contains an N-terminal DNA binding domain and C-terminal ligand binding domain and is localized to the nucleus, cytoplasm, and mitochondria. Upon binding to 17beta-estradiol or related ligands, the encoded protein forms homo- or hetero-dimers that interact with specific DNA sequences to activate transcription. Some isoforms dominantly inhibit the activity of other estrogen receptor family members. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been fully characterized. [provided by RefSeq, Jul 2008]","start":64084232,"end":64338112,"strand":-1,"description":"estrogen receptor 2 [Source:HGNC Symbol;Acc:HGNC:3468]"}, {"versioned_ensembl_gene_id":"ENSG00000103175.10","gene_symbol":"WFDC1","gene_name":"WAP four-disulfide core domain 1 [Source:HGNC Symbol;Acc:HGNC:15466]","synonyms":"PS20","biotype":"protein_coding","ncbi_id":"58189","summary":"This gene encodes a member of the WAP-type four disulfide core domain family. The WAP-type four-disulfide core domain contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many family members. This gene is mapped to chromosome 16q24, an area of frequent loss of heterozygosity in cancers, including prostate, breast and hepatocellular cancers and Wilms' tumor. This gene is downregulated in many cancer types and may be involved in the inhibition of cell proliferation. The encoded protein may also play a role in the susceptibility of certain CD4 memory T cells to human immunodeficiency virus infection. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":84294646,"end":84329851,"strand":1,"description":"WAP four-disulfide core domain 1 [Source:HGNC Symbol;Acc:HGNC:15466]"}, {"versioned_ensembl_gene_id":"ENSG00000186132.14","gene_symbol":"C2orf76","gene_name":"chromosome 2 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:27017]","synonyms":"AIM29,MGC104437,LOC130355","biotype":"protein_coding","ncbi_id":"130355","summary":null,"start":119302225,"end":119366828,"strand":-1,"description":"chromosome 2 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:27017]"}, {"versioned_ensembl_gene_id":"ENSG00000237827.1","gene_symbol":"RPS15AP29","gene_name":"ribosomal protein S15a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35981]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128863","summary":null,"start":103125017,"end":103125416,"strand":-1,"description":"ribosomal protein S15a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35981]"}, {"versioned_ensembl_gene_id":"ENSG00000175445.14","gene_symbol":"LPL","gene_name":"lipoprotein lipase [Source:HGNC Symbol;Acc:HGNC:6677]","synonyms":"LIPD","biotype":"protein_coding","ncbi_id":"4023","summary":"LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]","start":19901717,"end":19967258,"strand":1,"description":"lipoprotein lipase [Source:HGNC Symbol;Acc:HGNC:6677]"}, {"versioned_ensembl_gene_id":"ENSG00000205856.3","gene_symbol":"C22orf42","gene_name":"chromosome 22 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:27160]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150297","summary":null,"start":32149006,"end":32159322,"strand":-1,"description":"chromosome 22 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:27160]"}, {"versioned_ensembl_gene_id":"ENSG00000236560.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30061865,"end":30065490,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000223401.2","gene_symbol":"AC072022.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":187743686,"end":187746028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171827.10","gene_symbol":"ZNF570","gene_name":"zinc finger protein 570 [Source:HGNC Symbol;Acc:HGNC:26416]","synonyms":"FLJ30791","biotype":"protein_coding","ncbi_id":"148268","summary":null,"start":37467585,"end":37488652,"strand":1,"description":"zinc finger protein 570 [Source:HGNC Symbol;Acc:HGNC:26416]"}, {"versioned_ensembl_gene_id":"ENSG00000228804.5","gene_symbol":"AC072022.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":187702313,"end":187733849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213083.3","gene_symbol":"AC010731.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206686517,"end":206687362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277366.1","gene_symbol":"CU457734.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268383,"end":54269416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253644.1","gene_symbol":"AP001208.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101387299,"end":101393186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229430.3","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31272464,"end":31273666,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000248717.1","gene_symbol":"LINC02222","gene_name":"long intergenic non-protein coding RNA 2222 [Source:HGNC Symbol;Acc:HGNC:53091]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377765","summary":null,"start":180684766,"end":180686546,"strand":1,"description":"long intergenic non-protein coding RNA 2222 [Source:HGNC Symbol;Acc:HGNC:53091]"}, {"versioned_ensembl_gene_id":"ENSG00000188487.11","gene_symbol":"INSC","gene_name":"INSC, spindle orientation adaptor protein [Source:HGNC Symbol;Acc:HGNC:33116]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387755","summary":"In Drosophila, neuroblasts divide asymmetrically into another neuroblast at the apical side and a smaller ganglion mother cell on the basal side. Cell polarization is precisely regulated by 2 apically localized multiprotein signaling complexes that are tethered by Inscuteable, which regulates their apical localization (Izaki et al., 2006 [PubMed 16458856]).[supplied by OMIM, Mar 2008]","start":15112424,"end":15247208,"strand":1,"description":"INSC, spindle orientation adaptor protein [Source:HGNC Symbol;Acc:HGNC:33116]"}, {"versioned_ensembl_gene_id":"ENSG00000254516.1","gene_symbol":"AC103798.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37938601,"end":37954663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254084.1","gene_symbol":"AP001208.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101411873,"end":101452452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119655.10","gene_symbol":"NPC2","gene_name":"NPC intracellular cholesterol transporter 2 [Source:HGNC Symbol;Acc:HGNC:14537]","synonyms":"NP-C2,HE1,EDDM1","biotype":"protein_coding","ncbi_id":"10577","summary":"This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008]","start":74476192,"end":74494177,"strand":-1,"description":"NPC intracellular cholesterol transporter 2 [Source:HGNC Symbol;Acc:HGNC:14537]"}, {"versioned_ensembl_gene_id":"ENSG00000181781.9","gene_symbol":"ODF3L2","gene_name":"outer dense fiber of sperm tails 3 like 2 [Source:HGNC Symbol;Acc:HGNC:26841]","synonyms":"FLJ40059,C19orf19","biotype":"protein_coding","ncbi_id":"284451","summary":null,"start":463346,"end":474983,"strand":-1,"description":"outer dense fiber of sperm tails 3 like 2 [Source:HGNC Symbol;Acc:HGNC:26841]"}, {"versioned_ensembl_gene_id":"ENSG00000236791.2","gene_symbol":"OR2AI1P","gene_name":"olfactory receptor family 2 subfamily AI member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15063]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"134082","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":180692832,"end":180693763,"strand":-1,"description":"olfactory receptor family 2 subfamily AI member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15063]"}, {"versioned_ensembl_gene_id":"ENSG00000169981.10","gene_symbol":"ZNF35","gene_name":"zinc finger protein 35 [Source:HGNC Symbol;Acc:HGNC:13099]","synonyms":"Zfp105,HF10,HF.10","biotype":"protein_coding","ncbi_id":"7584","summary":null,"start":44648727,"end":44660791,"strand":1,"description":"zinc finger protein 35 [Source:HGNC Symbol;Acc:HGNC:13099]"}, {"versioned_ensembl_gene_id":"ENSG00000279004.1","gene_symbol":"AC103798.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":38013510,"end":38014141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174339.2","gene_symbol":"OR2Y1","gene_name":"olfactory receptor family 2 subfamily Y member 1 [Source:HGNC Symbol;Acc:HGNC:14837]","synonyms":null,"biotype":"protein_coding","ncbi_id":"134083","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":180739042,"end":180740099,"strand":-1,"description":"olfactory receptor family 2 subfamily Y member 1 [Source:HGNC Symbol;Acc:HGNC:14837]"}, {"versioned_ensembl_gene_id":"ENSG00000254784.1","gene_symbol":"LRRC6P1","gene_name":"leucine rich repeat containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420589","summary":null,"start":38211389,"end":38212799,"strand":1,"description":"leucine rich repeat containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51151]"}, {"versioned_ensembl_gene_id":"ENSG00000256125.1","gene_symbol":"AC005868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126458462,"end":126458792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255477.1","gene_symbol":"AC021713.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38498995,"end":38500186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214043.7","gene_symbol":"LINC02347","gene_name":"long intergenic non-protein coding RNA 2347 [Source:HGNC Symbol;Acc:HGNC:53269]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128554","summary":null,"start":126442481,"end":126472790,"strand":1,"description":"long intergenic non-protein coding RNA 2347 [Source:HGNC Symbol;Acc:HGNC:53269]"}, {"versioned_ensembl_gene_id":"ENSG00000260530.1","gene_symbol":"AC010551.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84295498,"end":84296985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255175.5","gene_symbol":"AC022796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38618264,"end":38646356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273650.1","gene_symbol":"AC100793.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42751289,"end":42751717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260504.1","gene_symbol":"AC010551.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84342464,"end":84343407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214578.5","gene_symbol":"HMGN2P15","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39020]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288165","summary":null,"start":42753530,"end":42753799,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39020]"}, {"versioned_ensembl_gene_id":"ENSG00000249951.1","gene_symbol":"AC108067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94675245,"end":94702570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271868.1","gene_symbol":"AC114810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3496956,"end":3497428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236802.4","gene_symbol":"B3GALT4","gene_name":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]","synonyms":"beta3Gal-T4,GalT4","biotype":"protein_coding","ncbi_id":"8705","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is oriented telomere to centromere in close proximity to the ribosomal protein S18 gene. The functionality of the encoded protein is limited to ganglioseries glycolipid biosynthesis. [provided by RefSeq, Jul 2008]","start":33447505,"end":33449198,"strand":1,"description":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]"}, {"versioned_ensembl_gene_id":"ENSG00000197291.8","gene_symbol":"RAMP2-AS1","gene_name":"RAMP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44358]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100190938","summary":null,"start":42753914,"end":42761257,"strand":-1,"description":"RAMP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44358]"}, {"versioned_ensembl_gene_id":"ENSG00000233639.5","gene_symbol":"LINC01158","gene_name":"long intergenic non-protein coding RNA 1158 [Source:HGNC Symbol;Acc:HGNC:49513]","synonyms":"linc-Brn1a","biotype":"processed_transcript","ncbi_id":"100506421","summary":null,"start":104807572,"end":104853183,"strand":-1,"description":"long intergenic non-protein coding RNA 1158 [Source:HGNC Symbol;Acc:HGNC:49513]"}, {"versioned_ensembl_gene_id":"ENSG00000105438.8","gene_symbol":"KDELR1","gene_name":"KDEL endoplasmic reticulum protein retention receptor 1 [Source:HGNC Symbol;Acc:HGNC:6304]","synonyms":"HDEL,ERD2.1,ERD2","biotype":"protein_coding","ncbi_id":"10945","summary":"Retention of resident soluble proteins in the lumen of the endoplasmic reticulum (ER) is achieved in both yeast and animal cells by their continual retrieval from the cis-Golgi, or a pre-Golgi compartment. Sorting of these proteins is dependent on a C-terminal tetrapeptide signal, usually lys-asp-glu-leu (KDEL) in animal cells, and his-asp-glu-leu (HDEL) in S. cerevisiae. This process is mediated by a receptor that recognizes, and binds the tetrapeptide-containing protein, and returns it to the ER. In yeast, the sorting receptor encoded by a single gene, ERD2, which is a seven-transmembrane protein. Unlike yeast, several human homologs of the ERD2 gene, constituting the KDEL receptor gene family, have been described. The protein encoded by this gene was the first member of the family to be identified, and it encodes a protein structurally and functionally similar to the yeast ERD2 gene product. [provided by RefSeq, Jul 2008]","start":48382570,"end":48391553,"strand":-1,"description":"KDEL endoplasmic reticulum protein retention receptor 1 [Source:HGNC Symbol;Acc:HGNC:6304]"}, {"versioned_ensembl_gene_id":"ENSG00000235078.1","gene_symbol":"AC231981.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3519275,"end":3523197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239628.1","gene_symbol":"AC073288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170345678,"end":170353961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254024.1","gene_symbol":"AP001207.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101461177,"end":101492499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253991.1","gene_symbol":"AP001207.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101528723,"end":101529569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249599.1","gene_symbol":"BMPR1B-AS1","gene_name":"BMPR1B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50864]","synonyms":"TCONS_00007797","biotype":"lincRNA","ncbi_id":"100507012","summary":null,"start":94743800,"end":94757533,"strand":-1,"description":"BMPR1B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50864]"}, {"versioned_ensembl_gene_id":"ENSG00000253153.1","gene_symbol":"AP001207.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101562008,"end":101562488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135414.9","gene_symbol":"GDF11","gene_name":"growth differentiation factor 11 [Source:HGNC Symbol;Acc:HGNC:4216]","synonyms":"BMP-11","biotype":"protein_coding","ncbi_id":"10220","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein plays a role in the development of the nervous and other organ systems, and may regulate aging. [provided by RefSeq, Aug 2016]","start":55743280,"end":55757278,"strand":1,"description":"growth differentiation factor 11 [Source:HGNC Symbol;Acc:HGNC:4216]"}, {"versioned_ensembl_gene_id":"ENSG00000083307.10","gene_symbol":"GRHL2","gene_name":"grainyhead like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:2799]","synonyms":"TFCP2L3,FLJ13782,DFNA28,BOM","biotype":"protein_coding","ncbi_id":"79977","summary":"The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]","start":101492432,"end":101669726,"strand":1,"description":"grainyhead like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:2799]"}, {"versioned_ensembl_gene_id":"ENSG00000280161.1","gene_symbol":"AC022413.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":180810401,"end":180811384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182551.13","gene_symbol":"ADI1","gene_name":"acireductone dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:30576]","synonyms":"HMFT1638,FLJ10913,ARD,APL1,SIPL,mtnD,MTCBP-1","biotype":"protein_coding","ncbi_id":"55256","summary":"This gene encodes an enzyme that belongs to the aci-reductone dioxygenase family of metal-binding enzymes, which are involved in methionine salvage. This enzyme may regulate mRNA processing in the nucleus, and may carry out different functions depending on its localization. Related pseudogenes have been defined on chromosomes 8 and 20. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":3497361,"end":3519736,"strand":-1,"description":"acireductone dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:30576]"}, {"versioned_ensembl_gene_id":"ENSG00000226843.1","gene_symbol":"AL606753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208255290,"end":208255376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131446.16","gene_symbol":"MGAT1","gene_name":"mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7044]","synonyms":"GLYT1,GLCNAC-TI,MGAT,GnTI,GNT-1","biotype":"protein_coding","ncbi_id":"4245","summary":"There are believed to be over 100 different glycosyltransferases involved in the synthesis of protein-bound and lipid-bound oligosaccharides. UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I is a medial-Golgi enzyme essential for the synthesis of hybrid and complex N-glycans. The protein, encoded by a single exon, shows typical features of a type II transmembrane protein. The protein is believed to be essential for normal embryogenesis. Several variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":180784782,"end":180815652,"strand":-1,"description":"mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7044]"}, {"versioned_ensembl_gene_id":"ENSG00000258345.1","gene_symbol":"AC034102.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56118968,"end":56119939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256811.1","gene_symbol":"AC079360.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121856259,"end":121857059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255529.7","gene_symbol":"POLR2M","gene_name":"RNA polymerase II subunit M [Source:HGNC Symbol;Acc:HGNC:14862]","synonyms":"GRINL1A,Gdown1,Gdown,GCOM1","biotype":"protein_coding","ncbi_id":"81488","summary":"This gene encodes a subunit of a specific form of RNA polymerase II termed Pol II(G). The encoded protein may act as a negative regulator of transcriptional activation by the Mediator complex. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 4. Readthrough transcription between this gene and the neighboring upstream gene MYZAP (myocardial zonula adherens protein) is represented with GeneID 145781. [provided by RefSeq, Oct 2013]","start":57706629,"end":57782762,"strand":1,"description":"RNA polymerase II subunit M [Source:HGNC Symbol;Acc:HGNC:14862]"}, {"versioned_ensembl_gene_id":"ENSG00000158104.11","gene_symbol":"HPD","gene_name":"4-hydroxyphenylpyruvate dioxygenase [Source:HGNC Symbol;Acc:HGNC:5147]","synonyms":"PPD,GLOD3,4HPPD,4-HPPD","biotype":"protein_coding","ncbi_id":"3242","summary":"The protein encoded by this gene is an enzyme in the catabolic pathway of tyrosine. The encoded protein catalyzes the conversion of 4-hydroxyphenylpyruvate to homogentisate. Defects in this gene are a cause of tyrosinemia type 3 (TYRO3) and hawkinsinuria (HAWK). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":121839527,"end":121863596,"strand":-1,"description":"4-hydroxyphenylpyruvate dioxygenase [Source:HGNC Symbol;Acc:HGNC:5147]"}, {"versioned_ensembl_gene_id":"ENSG00000135482.6","gene_symbol":"ZC3H10","gene_name":"zinc finger CCCH-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25893]","synonyms":"ZC3HDC10,FLJ14451","biotype":"protein_coding","ncbi_id":"84872","summary":null,"start":56118159,"end":56127514,"strand":1,"description":"zinc finger CCCH-type containing 10 [Source:HGNC Symbol;Acc:HGNC:25893]"}, {"versioned_ensembl_gene_id":"ENSG00000174903.15","gene_symbol":"RAB1B","gene_name":"RAB1B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18370]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81876","summary":"Members of the RAB protein family, such as RAB1B, are low molecular mass monomeric GTPases localized on the cytoplasmic surfaces of distinct membrane-bound organelles. RAB1B functions in the early secretory pathway and is essential for vesicle transport between the endoplasmic reticulum (ER) and Golgi (Chen et al., 1997 [PubMed 9030196]; Alvarez et al., 2003 [PubMed 12802079]).[supplied by OMIM, Jan 2009]","start":66268533,"end":66277492,"strand":1,"description":"RAB1B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18370]"}, {"versioned_ensembl_gene_id":"ENSG00000245060.6","gene_symbol":"LINC00847","gene_name":"long intergenic non-protein coding RNA 847 [Source:HGNC Symbol;Acc:HGNC:45050]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729678","summary":null,"start":180830957,"end":180835726,"strand":1,"description":"long intergenic non-protein coding RNA 847 [Source:HGNC Symbol;Acc:HGNC:45050]"}, {"versioned_ensembl_gene_id":"ENSG00000259122.2","gene_symbol":"TVP23BP1","gene_name":"TVP23B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31127]","synonyms":"FAM18B3P","biotype":"unprocessed_pseudogene","ncbi_id":"100129124","summary":null,"start":26964917,"end":26970385,"strand":1,"description":"TVP23B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31127]"}, {"versioned_ensembl_gene_id":"ENSG00000205323.8","gene_symbol":"SARNP","gene_name":"SAP domain containing ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:24432]","synonyms":"THO1,Hcc-1,CIP29","biotype":"protein_coding","ncbi_id":"84324","summary":"This gene encodes a protein that is upregulated in response to various cytokines. The encoded protein may play a role in cell cycle progression. A translocation between this gene and the myeloid/lymphoid leukemia gene, resulting in expression of a chimeric protein, has been associated with acute myelomonocytic leukemia. Pseudogenes exist on chromosomes 7 and 8. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":55752463,"end":55817756,"strand":-1,"description":"SAP domain containing ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:24432]"}, {"versioned_ensembl_gene_id":"ENSG00000229281.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"PsiGPR53,dJ271M21.8","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537704,"end":29538787,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000279001.1","gene_symbol":"AC079602.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":121096027,"end":121096429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225077.2","gene_symbol":"LINC00337","gene_name":"long intergenic non-protein coding RNA 337 [Source:HGNC Symbol;Acc:HGNC:28620]","synonyms":"NCRNA00337,MGC40168,C1orf211","biotype":"lincRNA","ncbi_id":"148645","summary":null,"start":6236240,"end":6239444,"strand":1,"description":"long intergenic non-protein coding RNA 337 [Source:HGNC Symbol;Acc:HGNC:28620]"}, {"versioned_ensembl_gene_id":"ENSG00000134453.15","gene_symbol":"RBM17","gene_name":"RNA binding motif protein 17 [Source:HGNC Symbol;Acc:HGNC:16944]","synonyms":"SPF45,MGC14439","biotype":"protein_coding","ncbi_id":"84991","summary":"This gene encodes an RNA binding protein. The encoded protein is part of the spliceosome complex and functions in the second catalytic step of mRNA splicing. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 9 and 15. [provided by RefSeq, Mar 2009]","start":6088987,"end":6117457,"strand":1,"description":"RNA binding motif protein 17 [Source:HGNC Symbol;Acc:HGNC:16944]"}, {"versioned_ensembl_gene_id":"ENSG00000100557.9","gene_symbol":"C14orf105","gene_name":"chromosome 14 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:20189]","synonyms":"FLJ10650","biotype":"protein_coding","ncbi_id":"55195","summary":null,"start":57469301,"end":57493867,"strand":-1,"description":"chromosome 14 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:20189]"}, {"versioned_ensembl_gene_id":"ENSG00000258317.1","gene_symbol":"AC034102.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56120033,"end":56129619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234318.1","gene_symbol":"AC099794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62896009,"end":62901639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240790.1","gene_symbol":"AC073934.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127644685,"end":127652012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131477.10","gene_symbol":"RAMP2","gene_name":"receptor activity modifying protein 2 [Source:HGNC Symbol;Acc:HGNC:9844]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10266","summary":"The protein encoded by this gene is a member of the RAMP family of single-transmembrane-domain proteins, called receptor (calcitonin) activity modifying proteins (RAMPs). RAMPs are type I transmembrane proteins with an extracellular N terminus and a cytoplasmic C terminus. RAMPs are required to transport calcitonin-receptor-like receptor (CRLR) to the plasma membrane. CRLR, a receptor with seven transmembrane domains, can function as either a calcitonin-gene-related peptide (CGRP) receptor or an adrenomedullin receptor, depending on which members of the RAMP family are expressed. In the presence of this (RAMP2) protein, CRLR functions as an adrenomedullin receptor. The RAMP2 protein is involved in core glycosylation and transportation of adrenomedullin receptor to the cell surface. [provided by RefSeq, Jul 2008]","start":42758447,"end":42763041,"strand":1,"description":"receptor activity modifying protein 2 [Source:HGNC Symbol;Acc:HGNC:9844]"}, {"versioned_ensembl_gene_id":"ENSG00000272077.1","gene_symbol":"AC124045.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44667412,"end":44669364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237163.1","gene_symbol":"AC099794.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62905180,"end":62905482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214820.3","gene_symbol":"MPRIPP1","gene_name":"myosin phosphatase Rho interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44594]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421374","summary":null,"start":44579938,"end":44581026,"strand":-1,"description":"myosin phosphatase Rho interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44594]"}, {"versioned_ensembl_gene_id":"ENSG00000173673.7","gene_symbol":"HES3","gene_name":"hes family bHLH transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:26226]","synonyms":"bHLHb43","biotype":"protein_coding","ncbi_id":"390992","summary":null,"start":6244192,"end":6245578,"strand":1,"description":"hes family bHLH transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:26226]"}, {"versioned_ensembl_gene_id":"ENSG00000236869.1","gene_symbol":"AC099669.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44557357,"end":44685653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226493.1","gene_symbol":"RPL26P27","gene_name":"ribosomal protein L26 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36735]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271471","summary":null,"start":68499532,"end":68499968,"strand":1,"description":"ribosomal protein L26 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36735]"}, {"versioned_ensembl_gene_id":"ENSG00000186448.14","gene_symbol":"ZNF197","gene_name":"zinc finger protein 197 [Source:HGNC Symbol;Acc:HGNC:12988]","synonyms":"D3S1363E,ZSCAN41,ZNF166,ZKSCAN9,P18","biotype":"protein_coding","ncbi_id":"10168","summary":"This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein contains 20 tandemly arrayed C2H2-type zinc fingers, a Kruppel-associated box (KRAB) domain, and a SCAN box. This transcript turns over rapidly and contains 3' UTR AUUUA motifs, which are often a hallmark of rapid turnover. It is overexpressed in some thyroid papillary carcinomas. This gene is located in a cluster of zinc finger genes at 3p21. Naturally-occurring readthrough transcription is observed between this gene and the upstream zinc finger protein 660 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017]","start":44584888,"end":44648471,"strand":1,"description":"zinc finger protein 197 [Source:HGNC Symbol;Acc:HGNC:12988]"}, {"versioned_ensembl_gene_id":"ENSG00000122912.14","gene_symbol":"SLC25A16","gene_name":"solute carrier family 25 member 16 [Source:HGNC Symbol;Acc:HGNC:10986]","synonyms":"ML7,HGT.1,GDA,D10S105E","biotype":"protein_coding","ncbi_id":"8034","summary":"This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease. [provided by RefSeq, Jul 2008]","start":68477999,"end":68527474,"strand":-1,"description":"solute carrier family 25 member 16 [Source:HGNC Symbol;Acc:HGNC:10986]"}, {"versioned_ensembl_gene_id":"ENSG00000243095.1","gene_symbol":"RPL3P10","gene_name":"ribosomal protein L3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129004","summary":null,"start":39157538,"end":39158701,"strand":-1,"description":"ribosomal protein L3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36819]"}, {"versioned_ensembl_gene_id":"ENSG00000280433.1","gene_symbol":"FP565260.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5155499,"end":5165472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281970.1","gene_symbol":"TRBV6-1","gene_name":"T-cell receptor beta variable 6-1 [Source:HGNC Symbol;Acc:HGNC:12226]","synonyms":"TRBV61,TCRBV6S1,TCRBV13S3","biotype":"TR_V_gene","ncbi_id":"28606","summary":null,"start":142328321,"end":142328810,"strand":1,"description":"T-cell receptor beta variable 6-1 [Source:HGNC Symbol;Acc:HGNC:12226]"}, {"versioned_ensembl_gene_id":"ENSG00000197140.14","gene_symbol":"ADAM32","gene_name":"ADAM metallopeptidase domain 32 [Source:HGNC Symbol;Acc:HGNC:15479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203102","summary":"This gene encodes a member of the disintegrin family of membrane-anchored proteins that play a role in diverse biological processes such as brain development, fertilization, tumor development and inflammation. This gene is predominantly expressed in the testis. The encoded protein undergoes proteolytic processing to generate a mature polypeptide comprised of an metalloprotease, disintegrin and epidermal growth factor-like domains. This gene is located in a cluster of other disintegrin and metallopeptidase family genes on chromosome 8. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":39106990,"end":39284911,"strand":1,"description":"ADAM metallopeptidase domain 32 [Source:HGNC Symbol;Acc:HGNC:15479]"}, {"versioned_ensembl_gene_id":"ENSG00000158106.13","gene_symbol":"RHPN1","gene_name":"rhophilin Rho GTPase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19973]","synonyms":"RHPN,ODF5,KIAA1929","biotype":"protein_coding","ncbi_id":"114822","summary":null,"start":143368887,"end":143384220,"strand":1,"description":"rhophilin Rho GTPase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19973]"}, {"versioned_ensembl_gene_id":"ENSG00000174871.10","gene_symbol":"CNIH2","gene_name":"cornichon family AMPA receptor auxiliary protein 2 [Source:HGNC Symbol;Acc:HGNC:28744]","synonyms":"MGC50896,Cnil,CNIH-2","biotype":"protein_coding","ncbi_id":"254263","summary":"The protein encoded by this gene is an auxiliary subunit of the ionotropic glutamate receptor of the AMPA subtype. AMPA receptors mediate fast synaptic neurotransmission in the central nervous system. This protein has been reported to interact with the Type I AMPA receptor regulatory protein isoform gamma-8 to control assembly of hippocampal AMPA receptor complexes, thereby modulating receptor gating and pharmacology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":66278190,"end":66285301,"strand":1,"description":"cornichon family AMPA receptor auxiliary protein 2 [Source:HGNC Symbol;Acc:HGNC:28744]"}, {"versioned_ensembl_gene_id":"ENSG00000275970.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54873427,"end":54889651,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000240265.1","gene_symbol":"AC099328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69535664,"end":69536693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158292.6","gene_symbol":"GPR153","gene_name":"G protein-coupled receptor 153 [Source:HGNC Symbol;Acc:HGNC:23618]","synonyms":"PGR1","biotype":"protein_coding","ncbi_id":"387509","summary":"This gene encodes an integral membrane protein that belongs to the Class A rhodopsin superfamily of G protein coupled receptors. The encoded protein is expressed primarily in the central nervous system. A knockdown of the orthologous gene in rat is associated with a significant reduction in food intake and impaired decision making ability. Mutations in this gene are associated with schizophrenia, autism, and other neuropsychiatric disorders. The expression of this gene is activated by the glioma-associated oncogene homolog 1 transcription factor which, in turn, is activated by sonic hedgehog in normal and tumorigenic cells. [provided by RefSeq, Feb 2017]","start":6247346,"end":6260975,"strand":-1,"description":"G protein-coupled receptor 153 [Source:HGNC Symbol;Acc:HGNC:23618]"}, {"versioned_ensembl_gene_id":"ENSG00000114541.14","gene_symbol":"FRMD4B","gene_name":"FERM domain containing 4B [Source:HGNC Symbol;Acc:HGNC:24886]","synonyms":"KIAA1013,GRSP1","biotype":"protein_coding","ncbi_id":"23150","summary":"This gene encodes a GRP1-binding protein which contains a FERM protein interaction domain as well as two coiled coil domains. This protein may play a role as a scaffolding protein. [provided by RefSeq, Mar 2014]","start":69169990,"end":69542583,"strand":-1,"description":"FERM domain containing 4B [Source:HGNC Symbol;Acc:HGNC:24886]"}, {"versioned_ensembl_gene_id":"ENSG00000198130.15","gene_symbol":"HIBCH","gene_name":"3-hydroxyisobutyryl-CoA hydrolase [Source:HGNC Symbol;Acc:HGNC:4908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26275","summary":"This gene encodes the enzyme responsible for hydrolysis of both HIBYL-CoA and beta-hydroxypropionyl-CoA. Mutations in this gene have been associated with 3-hyroxyisobutyryl-CoA hydrolase deficiency. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":190189735,"end":190344193,"strand":-1,"description":"3-hydroxyisobutyryl-CoA hydrolase [Source:HGNC Symbol;Acc:HGNC:4908]"}, {"versioned_ensembl_gene_id":"ENSG00000278827.1","gene_symbol":"CU207370.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54360973,"end":54365019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198589.10","gene_symbol":"LRBA","gene_name":"LPS responsive beige-like anchor protein [Source:HGNC Symbol;Acc:HGNC:1742]","synonyms":"LBA,LAB300,CDC4L,BGL","biotype":"protein_coding","ncbi_id":"987","summary":"The protein encoded by this gene is a member of the WDL-BEACH-WD (WBW) gene family. Its expression is induced in B cells and macrophages by bacterial lipopolysaccharides (LPS). The encoded protein associates with protein kinase A and may be involved in leading intracellular vesicles to activated receptor complexes, which aids in the secretion and/or membrane deposition of immune effector molecules. Defects in this gene are associated with the disorder common variable immunodeficiency-8 with autoimmunity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":150264531,"end":151015727,"strand":-1,"description":"LPS responsive beige-like anchor protein [Source:HGNC Symbol;Acc:HGNC:1742]"}, {"versioned_ensembl_gene_id":"ENSG00000204071.10","gene_symbol":"TCEAL6","gene_name":"transcription elongation factor A like 6 [Source:HGNC Symbol;Acc:HGNC:24553]","synonyms":"WEX2","biotype":"protein_coding","ncbi_id":"158931","summary":null,"start":102140476,"end":102142970,"strand":-1,"description":"transcription elongation factor A like 6 [Source:HGNC Symbol;Acc:HGNC:24553]"}, {"versioned_ensembl_gene_id":"ENSG00000229103.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31279657,"end":31281111,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000168060.15","gene_symbol":"NAALADL1","gene_name":"N-acetylated alpha-linked acidic dipeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:23536]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10004","summary":null,"start":65044818,"end":65058549,"strand":-1,"description":"N-acetylated alpha-linked acidic dipeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:23536]"}, {"versioned_ensembl_gene_id":"ENSG00000188596.10","gene_symbol":"CFAP54","gene_name":"cilia and flagella associated protein 54 [Source:HGNC Symbol;Acc:HGNC:26456]","synonyms":"FLJ31514,C12orf63,C12orf55,FLJ44112","biotype":"protein_coding","ncbi_id":"144535","summary":null,"start":96489571,"end":96875555,"strand":1,"description":"cilia and flagella associated protein 54 [Source:HGNC Symbol;Acc:HGNC:26456]"}, {"versioned_ensembl_gene_id":"ENSG00000279669.1","gene_symbol":"AC079801.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5232668,"end":5243833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231710.1","gene_symbol":"CR759814.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31299956,"end":31300690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253775.1","gene_symbol":"AC100802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20079305,"end":20118442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242709.1","gene_symbol":"RPL30P9","gene_name":"ribosomal protein L30 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35763]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270981","summary":null,"start":20113343,"end":20113672,"strand":-1,"description":"ribosomal protein L30 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35763]"}, {"versioned_ensembl_gene_id":"ENSG00000235122.3","gene_symbol":"AL121974.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49817430,"end":49820442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279094.3","gene_symbol":"LINC01670","gene_name":"long intergenic non-protein coding RNA 1670 [Source:HGNC Symbol;Acc:HGNC:52458]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379487","summary":null,"start":5499151,"end":5502542,"strand":-1,"description":"long intergenic non-protein coding RNA 1670 [Source:HGNC Symbol;Acc:HGNC:52458]"}, {"versioned_ensembl_gene_id":"ENSG00000223538.2","gene_symbol":"AC079602.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121107220,"end":121107490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250563.1","gene_symbol":"KNOP1P5","gene_name":"lysine rich nucleolar protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130158","summary":null,"start":126072587,"end":126074231,"strand":1,"description":"lysine rich nucleolar protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48923]"}, {"versioned_ensembl_gene_id":"ENSG00000278970.1","gene_symbol":"HEIH","gene_name":"hepatocellular carcinoma up-regulated EZH2-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:45049]","synonyms":"lncRNA-HEIH,LINC00848,LINC-HEIH,HCCAT2","biotype":"TEC","ncbi_id":"100859930","summary":null,"start":180829954,"end":180831605,"strand":-1,"description":"hepatocellular carcinoma up-regulated EZH2-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:45049]"}, {"versioned_ensembl_gene_id":"ENSG00000226707.1","gene_symbol":"AL359458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49823712,"end":49824782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253841.1","gene_symbol":"AC024681.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126073046,"end":126073532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229537.6","gene_symbol":"LINC01739","gene_name":"long intergenic non-protein coding RNA 1739 [Source:HGNC Symbol;Acc:HGNC:52527]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378769","summary":null,"start":62975751,"end":63022504,"strand":-1,"description":"long intergenic non-protein coding RNA 1739 [Source:HGNC Symbol;Acc:HGNC:52527]"}, {"versioned_ensembl_gene_id":"ENSG00000278842.1","gene_symbol":"AC008147.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50286244,"end":50289231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115138.10","gene_symbol":"POMC","gene_name":"proopiomelanocortin [Source:HGNC Symbol;Acc:HGNC:9201]","synonyms":"POC,NPP,MSH,LPH,CLIP,ACTH","biotype":"protein_coding","ncbi_id":"5443","summary":"This gene encodes a preproprotein that undergoes extensive, tissue-specific, post-translational processing via cleavage by subtilisin-like enzymes known as prohormone convertases. There are eight potential cleavage sites within the preproprotein and, depending on tissue type and the available convertases, processing may yield as many as ten biologically active peptides involved in diverse cellular functions. The encoded protein is synthesized mainly in corticotroph cells of the anterior pituitary where four cleavage sites are used; adrenocorticotrophin, essential for normal steroidogenesis and the maintenance of normal adrenal weight, and lipotropin beta are the major end products. In other tissues, including the hypothalamus, placenta, and epithelium, all cleavage sites may be used, giving rise to peptides with roles in pain and energy homeostasis, melanocyte stimulation, and immune modulation. These include several distinct melanotropins, lipotropins, and endorphins that are contained within the adrenocorticotrophin and beta-lipotropin peptides. The antimicrobial melanotropin alpha peptide exhibits antibacterial and antifungal activity. Mutations in this gene have been associated with early onset obesity, adrenal insufficiency, and red hair pigmentation. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jan 2016]","start":25160853,"end":25168903,"strand":-1,"description":"proopiomelanocortin [Source:HGNC Symbol;Acc:HGNC:9201]"}, {"versioned_ensembl_gene_id":"ENSG00000102796.10","gene_symbol":"DHRS12","gene_name":"dehydrogenase/reductase 12 [Source:HGNC Symbol;Acc:HGNC:25832]","synonyms":"SDR40C1,FLJ13639","biotype":"protein_coding","ncbi_id":"79758","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family, which has over 46,000 members. Members in this family are enzymes that metabolize many different compounds, such as steroid hormones, prostaglandins, retinoids, lipids and xenobiotics. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":51767993,"end":51804157,"strand":-1,"description":"dehydrogenase/reductase 12 [Source:HGNC Symbol;Acc:HGNC:25832]"}, {"versioned_ensembl_gene_id":"ENSG00000227485.1","gene_symbol":"AL162400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63024207,"end":63025658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245156.1","gene_symbol":"AP001107.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66269832,"end":66278525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241026.1","gene_symbol":"AC105910.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22389865,"end":22390655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236424.7","gene_symbol":"TSPY10","gene_name":"testis specific protein, Y-linked 10 [Source:HGNC Symbol;Acc:HGNC:37473]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100289087","summary":null,"start":9527880,"end":9530682,"strand":1,"description":"testis specific protein, Y-linked 10 [Source:HGNC Symbol;Acc:HGNC:37473]"}, {"versioned_ensembl_gene_id":"ENSG00000229225.1","gene_symbol":"AL162400.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63078081,"end":63079031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196670.13","gene_symbol":"ZFP62","gene_name":"ZFP62 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23241]","synonyms":"ZNF755,ZET,FLJ34231","biotype":"protein_coding","ncbi_id":"643836","summary":null,"start":180847611,"end":180861285,"strand":-1,"description":"ZFP62 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23241]"}, {"versioned_ensembl_gene_id":"ENSG00000174851.15","gene_symbol":"YIF1A","gene_name":"Yip1 interacting factor homolog A, membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:16688]","synonyms":"YIF1P,YIF1,FinGER7,54TM","biotype":"protein_coding","ncbi_id":"10897","summary":null,"start":66284580,"end":66289170,"strand":-1,"description":"Yip1 interacting factor homolog A, membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:16688]"}, {"versioned_ensembl_gene_id":"ENSG00000174418.7","gene_symbol":"RPL35P9","gene_name":"ribosomal protein L35 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39402]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873796","summary":null,"start":106425773,"end":106426122,"strand":1,"description":"ribosomal protein L35 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39402]"}, {"versioned_ensembl_gene_id":"ENSG00000228883.9","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31716138,"end":31723494,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000248720.1","gene_symbol":"RFPL4AP5","gene_name":"ret finger protein like 4A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45144]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420058","summary":null,"start":126174186,"end":126175014,"strand":-1,"description":"ret finger protein like 4A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45144]"}, {"versioned_ensembl_gene_id":"ENSG00000223683.1","gene_symbol":"RPSAP65","gene_name":"ribosomal protein SA pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:51914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075109","summary":null,"start":63262113,"end":63262707,"strand":1,"description":"ribosomal protein SA pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:51914]"}, {"versioned_ensembl_gene_id":"ENSG00000244791.2","gene_symbol":"AC087667.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126325495,"end":126329535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255403.1","gene_symbol":"AP000641.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105706299,"end":105707937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203605.3","gene_symbol":"AC096543.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63139250,"end":63163153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229579.4","gene_symbol":"USP17L26","gene_name":"ubiquitin specific peptidase 17-like family member 26 [Source:HGNC Symbol;Acc:HGNC:44454]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728379","summary":null,"start":9334658,"end":9336609,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 26 [Source:HGNC Symbol;Acc:HGNC:44454]"}, {"versioned_ensembl_gene_id":"ENSG00000165898.13","gene_symbol":"ISCA2","gene_name":"iron-sulfur cluster assembly 2 [Source:HGNC Symbol;Acc:HGNC:19857]","synonyms":"ISA2,HBLD1","biotype":"protein_coding","ncbi_id":"122961","summary":"The protein encoded by this gene is an A-type iron-sulfur cluster (ISC) protein found in mitochondria. The encoded protein appears to be involved in the maturation of mitochondrial iron-sulfur proteins. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":74493720,"end":74497106,"strand":1,"description":"iron-sulfur cluster assembly 2 [Source:HGNC Symbol;Acc:HGNC:19857]"}, {"versioned_ensembl_gene_id":"ENSG00000228734.2","gene_symbol":"AC096543.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63249920,"end":63251771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224209.7","gene_symbol":"LINC00466","gene_name":"long intergenic non-protein coding RNA 466 [Source:HGNC Symbol;Acc:HGNC:27294]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"199899","summary":null,"start":63159087,"end":63317274,"strand":-1,"description":"long intergenic non-protein coding RNA 466 [Source:HGNC Symbol;Acc:HGNC:27294]"}, {"versioned_ensembl_gene_id":"ENSG00000152578.12","gene_symbol":"GRIA4","gene_name":"glutamate ionotropic receptor AMPA type subunit 4 [Source:HGNC Symbol;Acc:HGNC:4574]","synonyms":"GLURD,GLUR4,GluA4","biotype":"protein_coding","ncbi_id":"2893","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes composed of multiple subunits, arranged to form ligand-gated ion channels. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. The subunit encoded by this gene belongs to a family of AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate)-sensitive glutamate receptors, and is subject to RNA editing (AGA->GGA; R->G). Alternative splicing of this gene results in transcript variants encoding different isoforms, which may vary in their signal transduction properties. Some haplotypes of this gene show a positive association with schizophrenia. [provided by RefSeq, Jul 2008]","start":105609994,"end":105982092,"strand":1,"description":"glutamate ionotropic receptor AMPA type subunit 4 [Source:HGNC Symbol;Acc:HGNC:4574]"}, {"versioned_ensembl_gene_id":"ENSG00000274204.1","gene_symbol":"AL138689.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":106506046,"end":106506713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135387.20","gene_symbol":"CAPRIN1","gene_name":"cell cycle associated protein 1 [Source:HGNC Symbol;Acc:HGNC:6743]","synonyms":"caprin-1,RNG105,M11S1,GPIAP1","biotype":"protein_coding","ncbi_id":"4076","summary":null,"start":34051683,"end":34101156,"strand":1,"description":"cell cycle associated protein 1 [Source:HGNC Symbol;Acc:HGNC:6743]"}, {"versioned_ensembl_gene_id":"ENSG00000164054.15","gene_symbol":"SHISA5","gene_name":"shisa family member 5 [Source:HGNC Symbol;Acc:HGNC:30376]","synonyms":"SCOTIN,hShisa5","biotype":"protein_coding","ncbi_id":"51246","summary":"This gene encodes a member of the shisa family. The encoded protein is localized to the endoplasmic reticulum, and together with p53 induces apoptosis in a caspase-dependent manner. Alternative splicing results in multiple transcript variants. Related pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Apr 2016]","start":48467798,"end":48504826,"strand":-1,"description":"shisa family member 5 [Source:HGNC Symbol;Acc:HGNC:30376]"}, {"versioned_ensembl_gene_id":"ENSG00000125266.6","gene_symbol":"EFNB2","gene_name":"ephrin B2 [Source:HGNC Symbol;Acc:HGNC:3227]","synonyms":"MGC126227,MGC126226,LERK5,HTKL,Htk-L,EPLG5,MGC126228","biotype":"protein_coding","ncbi_id":"1948","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNB class ephrin which binds to the EPHB4 and EPHA3 receptors. [provided by RefSeq, Jul 2008]","start":106489731,"end":106535114,"strand":-1,"description":"ephrin B2 [Source:HGNC Symbol;Acc:HGNC:3227]"}, {"versioned_ensembl_gene_id":"ENSG00000239641.1","gene_symbol":"PLS1-AS1","gene_name":"PLS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40451]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873943","summary":null,"start":142654784,"end":142656745,"strand":-1,"description":"PLS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40451]"}, {"versioned_ensembl_gene_id":"ENSG00000271174.1","gene_symbol":"AC104440.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66622760,"end":66623102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141933.9","gene_symbol":"TPGS1","gene_name":"tubulin polyglutamylase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:25058]","synonyms":"PGs1,GTRGEO22,C19orf20","biotype":"protein_coding","ncbi_id":"91978","summary":null,"start":507497,"end":519654,"strand":1,"description":"tubulin polyglutamylase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:25058]"}, {"versioned_ensembl_gene_id":"ENSG00000254562.5","gene_symbol":"LINC01493","gene_name":"long intergenic non-protein coding RNA 1493 [Source:HGNC Symbol;Acc:HGNC:51150]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928536","summary":null,"start":38646476,"end":38674241,"strand":1,"description":"long intergenic non-protein coding RNA 1493 [Source:HGNC Symbol;Acc:HGNC:51150]"}, {"versioned_ensembl_gene_id":"ENSG00000204657.4","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29585121,"end":29590500,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000239576.1","gene_symbol":"COX6CP14","gene_name":"cytochrome c oxidase subunit 6C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481683","summary":null,"start":49758483,"end":49758656,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49366]"}, {"versioned_ensembl_gene_id":"ENSG00000244730.1","gene_symbol":"AC139451.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49775285,"end":49775614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241326.1","gene_symbol":"AL603962.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9983141,"end":9984568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228150.1","gene_symbol":"AL357140.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9942923,"end":9949974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176095.11","gene_symbol":"IP6K1","gene_name":"inositol hexakisphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:18360]","synonyms":"KIAA0263,IHPK1","biotype":"protein_coding","ncbi_id":"9807","summary":"This gene encodes a member of the inositol phosphokinase family. The encoded protein may be responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2011]","start":49724294,"end":49786542,"strand":-1,"description":"inositol hexakisphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:18360]"}, {"versioned_ensembl_gene_id":"ENSG00000099866.14","gene_symbol":"MADCAM1","gene_name":"mucosal vascular addressin cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:6765]","synonyms":"MACAM1","biotype":"protein_coding","ncbi_id":"8174","summary":"The protein encoded by this gene is an endothelial cell adhesion molecule that interacts preferentially with the leukocyte beta7 integrin LPAM-1 (alpha4beta7), L-selectin, and VLA-4 (alpha4beta1) on myeloid cells to direct leukocytes into mucosal and inflamed tissues. It is a member of the immunoglobulin family and is similar to ICAM1 and VCAM1. At least seven alternatively spliced transcripts encoding different protein isoforms have been found for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":489176,"end":505342,"strand":1,"description":"mucosal vascular addressin cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:6765]"}, {"versioned_ensembl_gene_id":"ENSG00000283611.1","gene_symbol":"AL357140.4","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":9951231,"end":9960832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240975.1","gene_symbol":"AC021723.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39161453,"end":39161967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253427.1","gene_symbol":"AC084116.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126474189,"end":126492596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227609.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"BPG126D10.10,OTTHUMG00000086663","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577459,"end":29577748,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000162441.11","gene_symbol":"LZIC","gene_name":"leucine zipper and CTNNBIP1 domain containing [Source:HGNC Symbol;Acc:HGNC:17497]","synonyms":"MGC15436","biotype":"protein_coding","ncbi_id":"84328","summary":null,"start":9922113,"end":9943407,"strand":-1,"description":"leucine zipper and CTNNBIP1 domain containing [Source:HGNC Symbol;Acc:HGNC:17497]"}, {"versioned_ensembl_gene_id":"ENSG00000270588.1","gene_symbol":"AC021749.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39873782,"end":39874388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253220.1","gene_symbol":"AC084116.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126498149,"end":126500303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258769.1","gene_symbol":"AC005479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74482985,"end":74483435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232173.2","gene_symbol":"AL645936.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573909,"end":29574836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206428.9","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"IRT-1,AIF-1,IBA1,Em:AF129756.17","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31605413,"end":31607250,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000231301.1","gene_symbol":"AL645936.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582508,"end":29583025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239263.1","gene_symbol":"RBM43P1","gene_name":"RNA binding motif protein 43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:46024]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131568","summary":null,"start":69471452,"end":69472532,"strand":-1,"description":"RNA binding motif protein 43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:46024]"}, {"versioned_ensembl_gene_id":"ENSG00000227159.8","gene_symbol":"DDX11L16","gene_name":"DEAD/H-box helicase 11 like 16 [Source:HGNC Symbol;Acc:HGNC:37115]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"727856","summary":null,"start":156025664,"end":156027877,"strand":-1,"description":"DEAD/H-box helicase 11 like 16 [Source:HGNC Symbol;Acc:HGNC:37115]"}, {"versioned_ensembl_gene_id":"ENSG00000213886.3","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555515,"end":29559925,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000198914.3","gene_symbol":"POU3F3","gene_name":"POU class 3 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:9216]","synonyms":"OTF8,BRN1","biotype":"protein_coding","ncbi_id":"5455","summary":"This gene encodes a POU-domain containing protein that functions as a transcription factor. The encoded protein recognizes an octamer sequence in the DNA of target genes. This protein may play a role in development of the nervous system. [provided by RefSeq, Apr 2015]","start":104855511,"end":104858574,"strand":1,"description":"POU class 3 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:9216]"}, {"versioned_ensembl_gene_id":"ENSG00000113303.11","gene_symbol":"BTNL8","gene_name":"butyrophilin like 8 [Source:HGNC Symbol;Acc:HGNC:26131]","synonyms":"FLJ21458,BTN9.2","biotype":"protein_coding","ncbi_id":"79908","summary":null,"start":180899077,"end":180950906,"strand":1,"description":"butyrophilin like 8 [Source:HGNC Symbol;Acc:HGNC:26131]"}, {"versioned_ensembl_gene_id":"ENSG00000184786.5","gene_symbol":"TCTE3","gene_name":"t-complex-associated-testis-expressed 3 [Source:HGNC Symbol;Acc:HGNC:11695]","synonyms":"TCTEX1D3","biotype":"protein_coding","ncbi_id":"6991","summary":null,"start":169740114,"end":169751587,"strand":-1,"description":"t-complex-associated-testis-expressed 3 [Source:HGNC Symbol;Acc:HGNC:11695]"}, {"versioned_ensembl_gene_id":"ENSG00000239587.1","gene_symbol":"AC018730.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104865407,"end":104867496,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269707.1","gene_symbol":"AC018730.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":104853285,"end":104926052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242086.8","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195739964,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000229743.2","gene_symbol":"LINC01159","gene_name":"long intergenic non-protein coding RNA 1159 [Source:HGNC Symbol;Acc:HGNC:49514]","synonyms":"linc-Brn1b","biotype":"processed_transcript","ncbi_id":"102682016","summary":null,"start":104865497,"end":104872595,"strand":-1,"description":"long intergenic non-protein coding RNA 1159 [Source:HGNC Symbol;Acc:HGNC:49514]"}, {"versioned_ensembl_gene_id":"ENSG00000204681.10","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"GPRC3A,hGB1a","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555629,"end":29633976,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000177105.9","gene_symbol":"RHOG","gene_name":"ras homolog family member G [Source:HGNC Symbol;Acc:HGNC:672]","synonyms":"MGC125836,MGC125835,ARHG,RhoG","biotype":"protein_coding","ncbi_id":"391","summary":"This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. The encoded protein facilitates translocation of a functional guanine nucleotide exchange factor (GEF) complex from the cytoplasm to the plasma membrane where ras-related C3 botulinum toxin substrate 1 is activated to promote lamellipodium formation and cell migration. Two related pseudogene have been identified on chromosomes 20 and X. [provided by RefSeq, Aug 2011]","start":3826978,"end":3840983,"strand":-1,"description":"ras homolog family member G [Source:HGNC Symbol;Acc:HGNC:672]"}, {"versioned_ensembl_gene_id":"ENSG00000281106.2","gene_symbol":"LINC00282","gene_name":"long intergenic non-protein coding RNA 282 [Source:HGNC Symbol;Acc:HGNC:26737]","synonyms":"NCRNA00282,FLJ37307","biotype":"protein_coding","ncbi_id":"283521","summary":null,"start":51813347,"end":51845175,"strand":-1,"description":"long intergenic non-protein coding RNA 282 [Source:HGNC Symbol;Acc:HGNC:26737]"}, {"versioned_ensembl_gene_id":"ENSG00000253530.1","gene_symbol":"AC084116.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126518698,"end":126522351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203761.5","gene_symbol":"MSTO2P","gene_name":"misato family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:26329]","synonyms":"MSTO2","biotype":"unprocessed_pseudogene","ncbi_id":"100129405","summary":null,"start":155745829,"end":155750137,"strand":1,"description":"misato family member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:26329]"}, {"versioned_ensembl_gene_id":"ENSG00000227140.3","gene_symbol":"USP17L5","gene_name":"ubiquitin specific peptidase 17-like family member 5 [Source:HGNC Symbol;Acc:HGNC:37177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728386","summary":null,"start":9339403,"end":9340995,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 5 [Source:HGNC Symbol;Acc:HGNC:37177]"}, {"versioned_ensembl_gene_id":"ENSG00000117906.13","gene_symbol":"RCN2","gene_name":"reticulocalbin 2 [Source:HGNC Symbol;Acc:HGNC:9935]","synonyms":"TCBP49,ERC55,ERC-55,E6BP","biotype":"protein_coding","ncbi_id":"5955","summary":"The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012]","start":76931619,"end":76954392,"strand":1,"description":"reticulocalbin 2 [Source:HGNC Symbol;Acc:HGNC:9935]"}, {"versioned_ensembl_gene_id":"ENSG00000231856.2","gene_symbol":"AL162377.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51803838,"end":51813832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234937.1","gene_symbol":"AL139128.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155845367,"end":155846624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284709.1","gene_symbol":"KF456110.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81385390,"end":81385774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254286.5","gene_symbol":"AC083923.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126557875,"end":126713415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273920.1","gene_symbol":"AC103858.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81335577,"end":81336119,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111731.12","gene_symbol":"C2CD5","gene_name":"C2 calcium dependent domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29062]","synonyms":"CDP138,KIAA0528","biotype":"protein_coding","ncbi_id":"9847","summary":null,"start":22448583,"end":22544546,"strand":-1,"description":"C2 calcium dependent domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29062]"}, {"versioned_ensembl_gene_id":"ENSG00000157657.14","gene_symbol":"ZNF618","gene_name":"zinc finger protein 618 [Source:HGNC Symbol;Acc:HGNC:29416]","synonyms":"NEDD10,KIAA1952","biotype":"protein_coding","ncbi_id":"114991","summary":null,"start":113876282,"end":114056591,"strand":1,"description":"zinc finger protein 618 [Source:HGNC Symbol;Acc:HGNC:29416]"}, {"versioned_ensembl_gene_id":"ENSG00000259343.6","gene_symbol":"TMC3-AS1","gene_name":"TMC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51424]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929655","summary":null,"start":81324377,"end":81518200,"strand":1,"description":"TMC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51424]"}, {"versioned_ensembl_gene_id":"ENSG00000138400.12","gene_symbol":"MDH1B","gene_name":"malate dehydrogenase 1B [Source:HGNC Symbol;Acc:HGNC:17836]","synonyms":"RP11-95H11,FLJ25341","biotype":"protein_coding","ncbi_id":"130752","summary":null,"start":206737763,"end":206765547,"strand":-1,"description":"malate dehydrogenase 1B [Source:HGNC Symbol;Acc:HGNC:17836]"}, {"versioned_ensembl_gene_id":"ENSG00000116580.18","gene_symbol":"GON4L","gene_name":"gon-4 like [Source:HGNC Symbol;Acc:HGNC:25973]","synonyms":"YARP,GON4,GON-4,FLJ20203","biotype":"protein_coding","ncbi_id":"54856","summary":null,"start":155749662,"end":155859400,"strand":-1,"description":"gon-4 like [Source:HGNC Symbol;Acc:HGNC:25973]"}, {"versioned_ensembl_gene_id":"ENSG00000254010.1","gene_symbol":"AC084116.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126556896,"end":126557433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253543.1","gene_symbol":"AC083923.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126582631,"end":126583006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168672.3","gene_symbol":"FAM84B","gene_name":"family with sequence similarity 84 member B [Source:HGNC Symbol;Acc:HGNC:24166]","synonyms":"NSE2,BCMP101","biotype":"protein_coding","ncbi_id":"157638","summary":null,"start":126552442,"end":126558393,"strand":-1,"description":"family with sequence similarity 84 member B [Source:HGNC Symbol;Acc:HGNC:24166]"}, {"versioned_ensembl_gene_id":"ENSG00000158220.13","gene_symbol":"ESYT3","gene_name":"extended synaptotagmin 3 [Source:HGNC Symbol;Acc:HGNC:24295]","synonyms":"CHR3SYT,FAM62C","biotype":"protein_coding","ncbi_id":"83850","summary":null,"start":138434586,"end":138481686,"strand":1,"description":"extended synaptotagmin 3 [Source:HGNC Symbol;Acc:HGNC:24295]"}, {"versioned_ensembl_gene_id":"ENSG00000127922.9","gene_symbol":"SEM1","gene_name":"SEM1, 26S proteasome complex subunit [Source:HGNC Symbol;Acc:HGNC:10845]","synonyms":"SHSF1,SHFM1,Shfdg1,SHFD1,FLJ42280,ECD,DSS1,C7orf76","biotype":"protein_coding","ncbi_id":"7979","summary":"The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]","start":96481626,"end":96709891,"strand":-1,"description":"SEM1, 26S proteasome complex subunit [Source:HGNC Symbol;Acc:HGNC:10845]"}, {"versioned_ensembl_gene_id":"ENSG00000188869.12","gene_symbol":"TMC3","gene_name":"transmembrane channel like 3 [Source:HGNC Symbol;Acc:HGNC:22995]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342125","summary":null,"start":81331217,"end":81374213,"strand":-1,"description":"transmembrane channel like 3 [Source:HGNC Symbol;Acc:HGNC:22995]"}, {"versioned_ensembl_gene_id":"ENSG00000029153.14","gene_symbol":"ARNTL2","gene_name":"aryl hydrocarbon receptor nuclear translocator like 2 [Source:HGNC Symbol;Acc:HGNC:18984]","synonyms":"PASD9,MOP9,CLIF,BMAL2,bHLHe6","biotype":"protein_coding","ncbi_id":"56938","summary":"This gene encodes a basic helix-loop-helix transcription factor belonging to the PAS (PER, ARNT, SIM) superfamily. The PAS proteins play important roles in adaptation to low atmospheric and cellular oxygen levels, exposure to certain environmental pollutants, and diurnal oscillations in light and temperature. This protein forms a transcriptionally active heterodimer with the circadian CLOCK protein, the structurally related MOP4, and hypoxia-inducible factors, such as HIF1alpha. Consistent with its role as a biologically relevant partner of circadian and hypoxia factors, this protein is coexpressed in regions of the brain such as the thalamus, hypothalamus, and amygdala. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":27332854,"end":27425289,"strand":1,"description":"aryl hydrocarbon receptor nuclear translocator like 2 [Source:HGNC Symbol;Acc:HGNC:18984]"}, {"versioned_ensembl_gene_id":"ENSG00000261453.1","gene_symbol":"LINC01735","gene_name":"long intergenic non-protein coding RNA 1735 [Source:HGNC Symbol;Acc:HGNC:52523]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985254","summary":null,"start":208607100,"end":208612192,"strand":-1,"description":"long intergenic non-protein coding RNA 1735 [Source:HGNC Symbol;Acc:HGNC:52523]"}, {"versioned_ensembl_gene_id":"ENSG00000259815.1","gene_symbol":"AC099793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":208626741,"end":208628085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171530.13","gene_symbol":"TBCA","gene_name":"tubulin folding cofactor A [Source:HGNC Symbol;Acc:HGNC:11579]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6902","summary":"The product of this gene is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. This gene encodes chaperonin cofactor A. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":77691166,"end":77868780,"strand":-1,"description":"tubulin folding cofactor A [Source:HGNC Symbol;Acc:HGNC:11579]"}, {"versioned_ensembl_gene_id":"ENSG00000227887.1","gene_symbol":"RPS26P13","gene_name":"ribosomal protein S26 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271106","summary":null,"start":208697369,"end":208697698,"strand":-1,"description":"ribosomal protein S26 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35784]"}, {"versioned_ensembl_gene_id":"ENSG00000254452.1","gene_symbol":"AP001107.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66276779,"end":66277492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232812.1","gene_symbol":"LINC01717","gene_name":"long intergenic non-protein coding RNA 1717 [Source:HGNC Symbol;Acc:HGNC:52504]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372893","summary":null,"start":208728688,"end":208733184,"strand":1,"description":"long intergenic non-protein coding RNA 1717 [Source:HGNC Symbol;Acc:HGNC:52504]"}, {"versioned_ensembl_gene_id":"ENSG00000249005.3","gene_symbol":"FAM90A4P","gene_name":"family with sequence similarity 90 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:32252]","synonyms":"FAM90A4","biotype":"unprocessed_pseudogene","ncbi_id":"441313","summary":null,"start":7272148,"end":7275158,"strand":1,"description":"family with sequence similarity 90 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:32252]"}, {"versioned_ensembl_gene_id":"ENSG00000259092.1","gene_symbol":"TRAV30","gene_name":"T-cell receptor alpha variable 30 [Source:HGNC Symbol;Acc:HGNC:12129]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28652","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22168429,"end":22168988,"strand":1,"description":"T-cell receptor alpha variable 30 [Source:HGNC Symbol;Acc:HGNC:12129]"}, {"versioned_ensembl_gene_id":"ENSG00000270726.6","gene_symbol":"AJ271736.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":156004218,"end":156022236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236950.1","gene_symbol":"LINC01774","gene_name":"long intergenic non-protein coding RNA 1774 [Source:HGNC Symbol;Acc:HGNC:52564]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372894","summary":null,"start":208972454,"end":208975307,"strand":1,"description":"long intergenic non-protein coding RNA 1774 [Source:HGNC Symbol;Acc:HGNC:52564]"}, {"versioned_ensembl_gene_id":"ENSG00000266933.2","gene_symbol":"AC005775.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":490046,"end":507833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185203.12","gene_symbol":"WASIR1","gene_name":"WASH and IL9R antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38513]","synonyms":"NCRNA00286B","biotype":"antisense_RNA","ncbi_id":"100128260","summary":null,"start":156014623,"end":156016837,"strand":-1,"description":"WASH and IL9R antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38513]"}, {"versioned_ensembl_gene_id":"ENSG00000237110.2","gene_symbol":"TAAR9","gene_name":"trace amine associated receptor 9 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:20977]","synonyms":"TAR3,TA3,TRAR3","biotype":"protein_coding","ncbi_id":"134860","summary":"TAAR9 is a member of a large family of rhodopsin G protein-coupled receptors (GPCRs, or GPRs). GPCRs contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins.[supplied by OMIM, Jul 2005]","start":132538290,"end":132539336,"strand":1,"description":"trace amine associated receptor 9 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:20977]"}, {"versioned_ensembl_gene_id":"ENSG00000231866.2","gene_symbol":"AC099677.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52925249,"end":52925423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230953.2","gene_symbol":"AC099677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52920422,"end":52920596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281794.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195739964,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000278684.1","gene_symbol":"AC104465.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":209001338,"end":209001476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173614.13","gene_symbol":"NMNAT1","gene_name":"nicotinamide nucleotide adenylyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17877]","synonyms":"PNAT1,NMNAT,LCA9","biotype":"protein_coding","ncbi_id":"64802","summary":"This gene encodes an enzyme which catalyzes a key step in the biosynthesis of nicotinamide adenine dinucleotide (NAD). The encoded enzyme is one of several nicotinamide nucleotide adenylyltransferases, and is specifically localized to the cell nucleus. Activity of this protein leads to the activation of a nuclear deacetylase that functions in the protection of damaged neurons. Mutations in this gene have been associated with Leber congenital amaurosis 9. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are located on chromosomes 1, 3, 4, 14, and 15. [provided by RefSeq, Jul 2014]","start":9943428,"end":9985501,"strand":1,"description":"nicotinamide nucleotide adenylyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17877]"}, {"versioned_ensembl_gene_id":"ENSG00000182484.15","gene_symbol":"WASH6P","gene_name":"WAS protein family homolog 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:31685]","synonyms":"FAM39A,CXYorf1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653440","summary":null,"start":156020826,"end":156025710,"strand":1,"description":"WAS protein family homolog 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:31685]"}, {"versioned_ensembl_gene_id":"ENSG00000232537.1","gene_symbol":"AC092810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":209147267,"end":209155101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121310.16","gene_symbol":"ECHDC2","gene_name":"enoyl-CoA hydratase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23408]","synonyms":"FLJ10948","biotype":"protein_coding","ncbi_id":"55268","summary":null,"start":52895910,"end":52927212,"strand":-1,"description":"enoyl-CoA hydratase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23408]"}, {"versioned_ensembl_gene_id":"ENSG00000152056.16","gene_symbol":"AP1S3","gene_name":"adaptor related protein complex 1 sigma 3 subunit [Source:HGNC Symbol;Acc:HGNC:18971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130340","summary":"This gene encodes a member of the adaptor-related protein complex 1, sigma subunit genes. The encoded protein is a component of adaptor protein complex 1 (AP-1), one of the AP complexes involved in claathrin-mediated vesicular transport from the Golgi or endosomes. Disruption of the pathway for display of HIV-1 antigens, which prevents recognition of the virus by cytotoxic T cells, has been shown to involve the AP-1 complex (PMID: 15569716). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":223751686,"end":223838027,"strand":-1,"description":"adaptor related protein complex 1 sigma 3 subunit [Source:HGNC Symbol;Acc:HGNC:18971]"}, {"versioned_ensembl_gene_id":"ENSG00000228081.2","gene_symbol":"AC092810.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":209173014,"end":209173375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224540.1","gene_symbol":"AC092810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":209232196,"end":209233419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282225.1","gene_symbol":"TRBV7-1","gene_name":"T-cell receptor beta variable 7-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12235]","synonyms":"TRBV71,TCRBV7S1,TCRBV6S7P","biotype":"TR_V_gene","ncbi_id":"28597","summary":null,"start":142332206,"end":142332727,"strand":1,"description":"T-cell receptor beta variable 7-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12235]"}, {"versioned_ensembl_gene_id":"ENSG00000225712.1","gene_symbol":"ATP5G2P1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:844]","synonyms":"ATP5GP1","biotype":"processed_pseudogene","ncbi_id":"520","summary":null,"start":209267798,"end":209268223,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:844]"}, {"versioned_ensembl_gene_id":"ENSG00000180638.17","gene_symbol":"SLC47A2","gene_name":"solute carrier family 47 member 2 [Source:HGNC Symbol;Acc:HGNC:26439]","synonyms":"FLJ31196,MATE2-K,MATE2","biotype":"protein_coding","ncbi_id":"146802","summary":"This gene encodes a protein belonging to a family of transporters involved in excretion of toxic electrolytes, both endogenous and exogenous, through urine and bile. This transporter family shares homology with the bacterial MATE (multidrug and toxin extrusion) protein family responsible for drug resistance. This gene is one of two members of the MATE transporter family located near each other on chromosome 17. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":19678288,"end":19718979,"strand":-1,"description":"solute carrier family 47 member 2 [Source:HGNC Symbol;Acc:HGNC:26439]"}, {"versioned_ensembl_gene_id":"ENSG00000227940.1","gene_symbol":"LINC01696","gene_name":"long intergenic non-protein coding RNA 1696 [Source:HGNC Symbol;Acc:HGNC:52484]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372897","summary":null,"start":209325456,"end":209328532,"strand":1,"description":"long intergenic non-protein coding RNA 1696 [Source:HGNC Symbol;Acc:HGNC:52484]"}, {"versioned_ensembl_gene_id":"ENSG00000183281.14","gene_symbol":"PLGLB1","gene_name":"plasminogen-like B1 [Source:HGNC Symbol;Acc:HGNC:9072]","synonyms":"PRP-B,PLGL","biotype":"protein_coding","ncbi_id":"5343","summary":null,"start":87002559,"end":87021852,"strand":-1,"description":"plasminogen-like B1 [Source:HGNC Symbol;Acc:HGNC:9072]"}, {"versioned_ensembl_gene_id":"ENSG00000231648.1","gene_symbol":"LINC01698","gene_name":"long intergenic non-protein coding RNA 1698 [Source:HGNC Symbol;Acc:HGNC:52486]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929476","summary":null,"start":209367662,"end":209379690,"strand":1,"description":"long intergenic non-protein coding RNA 1698 [Source:HGNC Symbol;Acc:HGNC:52486]"}, {"versioned_ensembl_gene_id":"ENSG00000180245.4","gene_symbol":"RRH","gene_name":"retinal pigment epithelium-derived rhodopsin homolog [Source:HGNC Symbol;Acc:HGNC:10450]","synonyms":"peropsin","biotype":"protein_coding","ncbi_id":"10692","summary":"Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This gene belongs to the seven-exon subfamily of mammalian opsin genes that includes opsin 5 and retinal G protein coupled receptor. [provided by RefSeq, Jul 2008]","start":109827994,"end":109844604,"strand":1,"description":"retinal pigment epithelium-derived rhodopsin homolog [Source:HGNC Symbol;Acc:HGNC:10450]"}, {"versioned_ensembl_gene_id":"ENSG00000282285.1","gene_symbol":"TRBV4-2","gene_name":"T-cell receptor beta variable 4-2 [Source:HGNC Symbol;Acc:HGNC:12216]","synonyms":"TRBV42,TCRBV7S3A2T,TCRBV4S2","biotype":"TR_V_gene","ncbi_id":"28616","summary":null,"start":142345452,"end":142346016,"strand":1,"description":"T-cell receptor beta variable 4-2 [Source:HGNC Symbol;Acc:HGNC:12216]"}, {"versioned_ensembl_gene_id":"ENSG00000256739.1","gene_symbol":"AP002892.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72351347,"end":72353210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255843.1","gene_symbol":"AP000593.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72302139,"end":72302965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172497.8","gene_symbol":"ACOT12","gene_name":"acyl-CoA thioesterase 12 [Source:HGNC Symbol;Acc:HGNC:24436]","synonyms":"THEAL,STARD15,Cach","biotype":"protein_coding","ncbi_id":"134526","summary":null,"start":81330005,"end":81394179,"strand":-1,"description":"acyl-CoA thioesterase 12 [Source:HGNC Symbol;Acc:HGNC:24436]"}, {"versioned_ensembl_gene_id":"ENSG00000259610.1","gene_symbol":"AC023034.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81633887,"end":81642190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259692.5","gene_symbol":"AC104041.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81660482,"end":81871125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162129.12","gene_symbol":"CLPB","gene_name":"ClpB homolog, mitochondrial AAA ATPase chaperonin [Source:HGNC Symbol;Acc:HGNC:30664]","synonyms":"SKD3,HSP78,FLJ13152,ANKCLB","biotype":"protein_coding","ncbi_id":"81570","summary":"This gene belongs to the ATP-ases associated with diverse cellular activities (AAA+) superfamily. Members of this superfamily form ring-shaped homo-hexamers and have highly conserved ATPase domains that are involved in various processes including DNA replication, protein degradation and reactivation of misfolded proteins. All members of this family hydrolyze ATP through their AAA+ domains and use the energy generated through ATP hydrolysis to exert mechanical force on their substrates. In addition to an AAA+ domain, the protein encoded by this gene contains a C-terminal D2 domain, which is characteristic of the AAA+ subfamily of Caseinolytic peptidases to which this protein belongs. It cooperates with Hsp70 in the disaggregation of protein aggregates. Allelic variants of this gene are associated with 3-methylglutaconic aciduria, which causes cataracts and neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":72292425,"end":72434680,"strand":-1,"description":"ClpB homolog, mitochondrial AAA ATPase chaperonin [Source:HGNC Symbol;Acc:HGNC:30664]"}, {"versioned_ensembl_gene_id":"ENSG00000223885.4","gene_symbol":"FAM90A13P","gene_name":"family with sequence similarity 90 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32261]","synonyms":"FAM90A13","biotype":"unprocessed_pseudogene","ncbi_id":"441314","summary":"FAM90A13 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7279770,"end":7282780,"strand":1,"description":"family with sequence similarity 90 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32261]"}, {"versioned_ensembl_gene_id":"ENSG00000249048.2","gene_symbol":"TRAV31","gene_name":"T-cell receptor alpha variable 31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12130]","synonyms":"TCRAV31S1","biotype":"TR_V_pseudogene","ncbi_id":"28651","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22177273,"end":22177864,"strand":1,"description":"T-cell receptor alpha variable 31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12130]"}, {"versioned_ensembl_gene_id":"ENSG00000198173.4","gene_symbol":"FAM47C","gene_name":"family with sequence similarity 47 member C [Source:HGNC Symbol;Acc:HGNC:25301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"442444","summary":"This gene encodes a product belonging to a family of proteins with unknown function. The coding sequence of this family member includes several tandemly repeated regions. [provided by RefSeq, Sep 2011]","start":37008397,"end":37011666,"strand":1,"description":"family with sequence similarity 47 member C [Source:HGNC Symbol;Acc:HGNC:25301]"}, {"versioned_ensembl_gene_id":"ENSG00000275995.1","gene_symbol":"AC109809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81403026,"end":81403570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213763.4","gene_symbol":"ACTBP2","gene_name":"actin, beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:135]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"62","summary":null,"start":77784881,"end":77786003,"strand":1,"description":"actin, beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:135]"}, {"versioned_ensembl_gene_id":"ENSG00000167515.10","gene_symbol":"TRAPPC2L","gene_name":"trafficking protein particle complex 2 like [Source:HGNC Symbol;Acc:HGNC:30887]","synonyms":"HSPC176","biotype":"protein_coding","ncbi_id":"51693","summary":"This gene encodes a protein that interacts with the tethering factor trafficking protein particle (TRAPP complex). TRAPP complexes mediate the contact between vescicles and target membranes, and thus, are involved in vescicle-mediated transport of proteins and lipids. The encoded protein is related to the X-linked trafficking protein particle complex 2. A related pseudogene is located on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":88856220,"end":88862686,"strand":1,"description":"trafficking protein particle complex 2 like [Source:HGNC Symbol;Acc:HGNC:30887]"}, {"versioned_ensembl_gene_id":"ENSG00000258905.1","gene_symbol":"TRAV32","gene_name":"T-cell receptor alpha variable 32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12131]","synonyms":null,"biotype":"TR_V_pseudogene","ncbi_id":"28650","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22185562,"end":22186057,"strand":1,"description":"T-cell receptor alpha variable 32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12131]"}, {"versioned_ensembl_gene_id":"ENSG00000258812.1","gene_symbol":"TRAV33","gene_name":"T-cell receptor alpha variable 33 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12132]","synonyms":"C14orf12","biotype":"TR_V_pseudogene","ncbi_id":"28649","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22190158,"end":22190713,"strand":1,"description":"T-cell receptor alpha variable 33 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12132]"}, {"versioned_ensembl_gene_id":"ENSG00000244266.1","gene_symbol":"AC090058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50365652,"end":50366086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162840.4","gene_symbol":"MT2P1","gene_name":"metallothionein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7407]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"4503","summary":null,"start":68376323,"end":68376505,"strand":1,"description":"metallothionein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7407]"}, {"versioned_ensembl_gene_id":"ENSG00000185958.9","gene_symbol":"FAM186A","gene_name":"family with sequence similarity 186 member A [Source:HGNC Symbol;Acc:HGNC:26980]","synonyms":"LOC121006","biotype":"protein_coding","ncbi_id":"121006","summary":null,"start":50326230,"end":50396622,"strand":-1,"description":"family with sequence similarity 186 member A [Source:HGNC Symbol;Acc:HGNC:26980]"}, {"versioned_ensembl_gene_id":"ENSG00000253931.1","gene_symbol":"AC105118.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143412749,"end":143417054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282719.1","gene_symbol":"AC234635.5","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142349215,"end":142349695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142224.15","gene_symbol":"IL19","gene_name":"interleukin 19 [Source:HGNC Symbol;Acc:HGNC:5990]","synonyms":"ZMDA1,NG.1,MDA1,IL-19,IL-10C","biotype":"protein_coding","ncbi_id":"29949","summary":"The protein encoded by this gene is a cytokine that belongs to the IL10 cytokine subfamily. This cytokine is found to be preferentially expressed in monocytes. It can bind the IL20 receptor complex and lead to the activation of the signal transducer and activator of transcription 3 (STAT3). A similar cytokine in mouse is reported to up-regulate the expression of IL6 and TNF-alpha and induce apoptosis, which suggests a role of this cytokine in inflammatory responses. Alternatively spliced transcript variants encoding the distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":206798870,"end":206842981,"strand":1,"description":"interleukin 19 [Source:HGNC Symbol;Acc:HGNC:5990]"}, {"versioned_ensembl_gene_id":"ENSG00000254338.1","gene_symbol":"MAFA-AS1","gene_name":"MAFA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51203]","synonyms":"TCONS_00014882,RP11-909N17.3","biotype":"antisense_RNA","ncbi_id":"104326051","summary":null,"start":143417679,"end":143419150,"strand":1,"description":"MAFA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51203]"}, {"versioned_ensembl_gene_id":"ENSG00000118246.13","gene_symbol":"FASTKD2","gene_name":"FAST kinase domains 2 [Source:HGNC Symbol;Acc:HGNC:29160]","synonyms":"KIAA0971","biotype":"protein_coding","ncbi_id":"22868","summary":"This gene encodes a protein that is localized in the mitochondrial inner compartment and that may play a role in mitochondrial apoptosis. Nonsense mutations have been reported to result in cytochrome c oxidase deficiency. [provided by RefSeq, Oct 2008]","start":206765357,"end":206792509,"strand":1,"description":"FAST kinase domains 2 [Source:HGNC Symbol;Acc:HGNC:29160]"}, {"versioned_ensembl_gene_id":"ENSG00000215837.7","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000182759.3","gene_symbol":"MAFA","gene_name":"MAF bZIP transcription factor A [Source:HGNC Symbol;Acc:HGNC:23145]","synonyms":"RIPE3b1,hMafA","biotype":"protein_coding","ncbi_id":"389692","summary":"MAFA is a transcription factor that binds RIPE3b, a conserved enhancer element that regulates pancreatic beta cell-specific expression of the insulin gene (INS; MIM 176730) (Olbrot et al., 2002 [PubMed 12011435]).[supplied by OMIM, Mar 2008]","start":143419182,"end":143430406,"strand":-1,"description":"MAF bZIP transcription factor A [Source:HGNC Symbol;Acc:HGNC:23145]"}, {"versioned_ensembl_gene_id":"ENSG00000128604.19","gene_symbol":"IRF5","gene_name":"interferon regulatory factor 5 [Source:HGNC Symbol;Acc:HGNC:6120]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3663","summary":"This gene encodes a member of the interferon regulatory factor (IRF) family, a group of transcription factors with diverse roles, including virus-mediated activation of interferon, and modulation of cell growth, differentiation, apoptosis, and immune system activity. Members of the IRF family are characterized by a conserved N-terminal DNA-binding domain containing tryptophan (W) repeats. Alternative promoter use and alternative splicing result in multiple transcript variants, and a 30-nt indel polymorphism (SNP rs60344245) can result in loss of a 10-aa segment. [provided by RefSeq, Dec 2016]","start":128937612,"end":128950035,"strand":1,"description":"interferon regulatory factor 5 [Source:HGNC Symbol;Acc:HGNC:6120]"}, {"versioned_ensembl_gene_id":"ENSG00000206142.9","gene_symbol":"AP000552.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21300990,"end":21325042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176945.16","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195720882,"end":195741123,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000215373.4","gene_symbol":"FAM90A5P","gene_name":"family with sequence similarity 90 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32253]","synonyms":"FAM90A5","biotype":"unprocessed_pseudogene","ncbi_id":"441315","summary":"FAM90A5 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, May 2010]","start":7287392,"end":7290402,"strand":1,"description":"family with sequence similarity 90 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32253]"}, {"versioned_ensembl_gene_id":"ENSG00000231351.2","gene_symbol":"AC111200.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86930250,"end":86930754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168061.14","gene_symbol":"SAC3D1","gene_name":"SAC3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30179]","synonyms":"SHD1,HSU79266","biotype":"protein_coding","ncbi_id":"29901","summary":null,"start":65040901,"end":65044828,"strand":1,"description":"SAC3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30179]"}, {"versioned_ensembl_gene_id":"ENSG00000172116.21","gene_symbol":"CD8B","gene_name":"CD8b molecule [Source:HGNC Symbol;Acc:HGNC:1707]","synonyms":"CD8B1","biotype":"protein_coding","ncbi_id":"926","summary":"The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen, acting as a coreceptor, and the T-cell receptor on the T lymphocyte recognize antigens displayed by an antigen presenting cell (APC) in the context of class I MHC molecules. The functional coreceptor is either a homodimer composed of two alpha chains, or a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 beta chain isoforms. Multiple alternatively spliced transcript variants encoding distinct membrane associated or secreted isoforms have been described. A pseudogene, also located on chromosome 2, has been identified. [provided by RefSeq, May 2010]","start":86815339,"end":86861924,"strand":-1,"description":"CD8b molecule [Source:HGNC Symbol;Acc:HGNC:1707]"}, {"versioned_ensembl_gene_id":"ENSG00000228736.9","gene_symbol":"RGL2","gene_name":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]","synonyms":"RAB2L,KE1.5,HKE1.5","biotype":"protein_coding","ncbi_id":"5863","summary":null,"start":33461997,"end":33469667,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]"}, {"versioned_ensembl_gene_id":"ENSG00000282505.1","gene_symbol":"AC234635.2","gene_name":null,"synonyms":null,"biotype":"TR_V_pseudogene","ncbi_id":null,"summary":null,"start":142359222,"end":142359681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283426.1","gene_symbol":"AC233280.20","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":195701618,"end":195711643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158158.11","gene_symbol":"CNNM4","gene_name":"cyclin and CBS domain divalent metal cation transport mediator 4 [Source:HGNC Symbol;Acc:HGNC:105]","synonyms":"KIAA1592,ACDP4","biotype":"protein_coding","ncbi_id":"26504","summary":"This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]","start":96760902,"end":96811891,"strand":1,"description":"cyclin and CBS domain divalent metal cation transport mediator 4 [Source:HGNC Symbol;Acc:HGNC:105]"}, {"versioned_ensembl_gene_id":"ENSG00000161813.21","gene_symbol":"LARP4","gene_name":"La ribonucleoprotein domain family member 4 [Source:HGNC Symbol;Acc:HGNC:24320]","synonyms":"PP13296","biotype":"protein_coding","ncbi_id":"113251","summary":null,"start":50392383,"end":50480004,"strand":1,"description":"La ribonucleoprotein domain family member 4 [Source:HGNC Symbol;Acc:HGNC:24320]"}, {"versioned_ensembl_gene_id":"ENSG00000172464.3","gene_symbol":"OR5AP2","gene_name":"olfactory receptor family 5 subfamily AP member 2 [Source:HGNC Symbol;Acc:HGNC:15258]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338675","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56641466,"end":56642471,"strand":-1,"description":"olfactory receptor family 5 subfamily AP member 2 [Source:HGNC Symbol;Acc:HGNC:15258]"}, {"versioned_ensembl_gene_id":"ENSG00000162891.10","gene_symbol":"IL20","gene_name":"interleukin 20 [Source:HGNC Symbol;Acc:HGNC:6002]","synonyms":"ZCYTO10,IL10D,IL-20","biotype":"protein_coding","ncbi_id":"50604","summary":"The protein encoded by this gene is a cytokine structurally related to interleukin 10 (IL10). This cytokine has been shown to transduce its signal through signal transducer and activator of transcription 3 (STAT3) in keratinocytes. A specific receptor for this cytokine is found to be expressed in skin and upregulated dramatically in psoriatic skin, suggesting a role for this protein in epidermal function and psoriasis. [provided by RefSeq, Jul 2008]","start":206865354,"end":206869223,"strand":1,"description":"interleukin 20 [Source:HGNC Symbol;Acc:HGNC:6002]"}, {"versioned_ensembl_gene_id":"ENSG00000255232.1","gene_symbol":"AC087441.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3961277,"end":3961538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227716.1","gene_symbol":"AP000459.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23477641,"end":23490724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124334.17","gene_symbol":"IL9R","gene_name":"interleukin 9 receptor [Source:HGNC Symbol;Acc:HGNC:6030]","synonyms":"CD129","biotype":"protein_coding","ncbi_id":"3581","summary":"The protein encoded by this gene is a cytokine receptor that specifically mediates the biological effects of interleukin 9 (IL9). The functional IL9 receptor complex requires this protein as well as the interleukin 2 receptor, gamma (IL2RG), a common gamma subunit shared by the receptors of many different cytokines. The ligand binding of this receptor leads to the activation of various JAK kinases and STAT proteins, which connect to different biologic responses. This gene is located at the pseudoautosomal regions of X and Y chromosomes. Genetic studies suggested an association of this gene with the development of asthma. Multiple pseudogenes on chromosome 9, 10, 16, and 18 have been described. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":155997581,"end":156010817,"strand":1,"description":"interleukin 9 receptor [Source:HGNC Symbol;Acc:HGNC:6030]"}, {"versioned_ensembl_gene_id":"ENSG00000172459.4","gene_symbol":"OR5AR1","gene_name":"olfactory receptor family 5 subfamily AR member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15260]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"219493","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":56663662,"end":56664687,"strand":1,"description":"olfactory receptor family 5 subfamily AR member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15260]"}, {"versioned_ensembl_gene_id":"ENSG00000233295.3","gene_symbol":"FAM90A20P","gene_name":"family with sequence similarity 90 member A20, pseudogene [Source:HGNC Symbol;Acc:HGNC:32268]","synonyms":"FAM90A20","biotype":"unprocessed_pseudogene","ncbi_id":"728430","summary":"FAM90A20 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7295014,"end":7298024,"strand":1,"description":"family with sequence similarity 90 member A20, pseudogene [Source:HGNC Symbol;Acc:HGNC:32268]"}, {"versioned_ensembl_gene_id":"ENSG00000236030.1","gene_symbol":"LINC01036","gene_name":"long intergenic non-protein coding RNA 1036 [Source:HGNC Symbol;Acc:HGNC:49024]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104169671","summary":null,"start":187092842,"end":187360323,"strand":1,"description":"long intergenic non-protein coding RNA 1036 [Source:HGNC Symbol;Acc:HGNC:49024]"}, {"versioned_ensembl_gene_id":"ENSG00000231599.1","gene_symbol":"LINC01037","gene_name":"long intergenic non-protein coding RNA 1037 [Source:HGNC Symbol;Acc:HGNC:49025]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144535","summary":null,"start":187443606,"end":187477222,"strand":1,"description":"long intergenic non-protein coding RNA 1037 [Source:HGNC Symbol;Acc:HGNC:49025]"}, {"versioned_ensembl_gene_id":"ENSG00000255141.1","gene_symbol":"HNRNPA1P76","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:48806]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480675","summary":null,"start":3972881,"end":3974237,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:48806]"}, {"versioned_ensembl_gene_id":"ENSG00000279796.1","gene_symbol":"AL133384.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":114424445,"end":114427398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232511.4","gene_symbol":"OR2AH1P","gene_name":"olfactory receptor family 2 subfamily AH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15144]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81336","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56667545,"end":56674664,"strand":-1,"description":"olfactory receptor family 2 subfamily AH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15144]"}, {"versioned_ensembl_gene_id":"ENSG00000272827.1","gene_symbol":"AL391813.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187480293,"end":187480614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240385.1","gene_symbol":"RPS29P20","gene_name":"ribosomal protein S29 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36491]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271587","summary":null,"start":4018948,"end":4019118,"strand":1,"description":"ribosomal protein S29 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36491]"}, {"versioned_ensembl_gene_id":"ENSG00000229368.1","gene_symbol":"AC090587.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3854612,"end":3855399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240579.1","gene_symbol":"AC006529.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127857852,"end":127858488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228661.1","gene_symbol":"AC090587.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3854318,"end":3855509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137509.10","gene_symbol":"PRCP","gene_name":"prolylcarboxypeptidase [Source:HGNC Symbol;Acc:HGNC:9344]","synonyms":"HUMPCP,PCP","biotype":"protein_coding","ncbi_id":"5547","summary":"This gene encodes a member of the peptidase S28 family of serine exopeptidases. The encoded preproprotein is proteolytically processed to generate the mature lysosomal prolylcarboxypeptidase. This enzyme cleaves C-terminal amino acids linked to proline in peptides such as angiotension II, III and des-Arg9-bradykinin. The cleavage occurs at acidic pH, but the enzyme activity is retained with some substrates at neutral pH. This enzyme has been shown to be an activator of the cell matrix-associated prekallikrein. The importance of angiotension II, one of the substrates of this enzyme, in regulating blood pressure and electrolyte balance suggests that this gene may be related to essential hypertension. A pseudogene of this gene has been identified on chromosome 2. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":82823502,"end":82970584,"strand":-1,"description":"prolylcarboxypeptidase [Source:HGNC Symbol;Acc:HGNC:9344]"}, {"versioned_ensembl_gene_id":"ENSG00000224336.2","gene_symbol":"FAM197Y1","gene_name":"family with sequence similarity 197 Y-linked member 1 [Source:HGNC Symbol;Acc:HGNC:37464]","synonyms":"FAM197Y1P","biotype":"unprocessed_pseudogene","ncbi_id":"100289265","summary":null,"start":9544917,"end":9547147,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 1 [Source:HGNC Symbol;Acc:HGNC:37464]"}, {"versioned_ensembl_gene_id":"ENSG00000197157.10","gene_symbol":"SND1","gene_name":"staphylococcal nuclease and tudor domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30646]","synonyms":"TDRD11,p100","biotype":"protein_coding","ncbi_id":"27044","summary":"This gene encodes a transcriptional co-activator that interacts with the acidic domain of Epstein-Barr virus nuclear antigen 2 (EBNA 2), a transcriptional activator that is required for B-lymphocyte transformation. Other transcription factors that interact with this protein are signal transducers and activators of transcription, STATs. This protein is also thought to be essential for normal cell growth. A similar protein in mammals and other organisms is a component of the RNA-induced silencing complex (RISC). [provided by RefSeq, Jul 2016]","start":127652180,"end":128092609,"strand":1,"description":"staphylococcal nuclease and tudor domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30646]"}, {"versioned_ensembl_gene_id":"ENSG00000237407.1","gene_symbol":"AP000552.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21312920,"end":21314904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135736.5","gene_symbol":"CCDC102A","gene_name":"coiled-coil domain containing 102A [Source:HGNC Symbol;Acc:HGNC:28097]","synonyms":"MGC10992","biotype":"protein_coding","ncbi_id":"92922","summary":null,"start":57512178,"end":57536599,"strand":-1,"description":"coiled-coil domain containing 102A [Source:HGNC Symbol;Acc:HGNC:28097]"}, {"versioned_ensembl_gene_id":"ENSG00000167323.11","gene_symbol":"STIM1","gene_name":"stromal interaction molecule 1 [Source:HGNC Symbol;Acc:HGNC:11386]","synonyms":"GOK,D11S4896E","biotype":"protein_coding","ncbi_id":"6786","summary":"This gene encodes a type 1 transmembrane protein that mediates Ca2+ influx after depletion of intracellular Ca2+ stores by gating of store-operated Ca2+ influx channels (SOCs). It is one of several genes located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocrotical carcinoma, and lung, ovarian, and breast cancer. This gene may play a role in malignancies and disease that involve this region, as well as early hematopoiesis, by mediating attachment to stromal cells. Mutations in this gene are associated with fatal classic Kaposi sarcoma, immunodeficiency due to defects in store-operated calcium entry (SOCE) in fibroblasts, ectodermal dysplasia and tubular aggregate myopathy. This gene is oriented in a head-to-tail configuration with the ribonucleotide reductase 1 gene (RRM1), with the 3' end of this gene situated 1.6 kb from the 5' end of the RRM1 gene. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":3854527,"end":4093210,"strand":1,"description":"stromal interaction molecule 1 [Source:HGNC Symbol;Acc:HGNC:11386]"}, {"versioned_ensembl_gene_id":"ENSG00000151812.14","gene_symbol":"SLC35F4","gene_name":"solute carrier family 35 member F4 [Source:HGNC Symbol;Acc:HGNC:19845]","synonyms":"FLJ37712,C14orf36","biotype":"protein_coding","ncbi_id":"341880","summary":null,"start":57563922,"end":57982194,"strand":-1,"description":"solute carrier family 35 member F4 [Source:HGNC Symbol;Acc:HGNC:19845]"}, {"versioned_ensembl_gene_id":"ENSG00000231986.1","gene_symbol":"AP000474.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23888798,"end":23890541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235780.3","gene_symbol":"USP17L27","gene_name":"ubiquitin specific peptidase 17-like family member 27 [Source:HGNC Symbol;Acc:HGNC:44455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728393","summary":null,"start":9344148,"end":9345740,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 27 [Source:HGNC Symbol;Acc:HGNC:44455]"}, {"versioned_ensembl_gene_id":"ENSG00000187699.10","gene_symbol":"C2orf88","gene_name":"chromosome 2 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:28191]","synonyms":"smAKAP,MGC13057","biotype":"protein_coding","ncbi_id":"84281","summary":null,"start":189879609,"end":190203484,"strand":1,"description":"chromosome 2 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:28191]"}, {"versioned_ensembl_gene_id":"ENSG00000231051.3","gene_symbol":"USP17L28","gene_name":"ubiquitin specific peptidase 17-like family member 28 [Source:HGNC Symbol;Acc:HGNC:44456]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728400","summary":null,"start":9348893,"end":9350485,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 28 [Source:HGNC Symbol;Acc:HGNC:44456]"}, {"versioned_ensembl_gene_id":"ENSG00000255099.1","gene_symbol":"AC023245.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109777912,"end":109782288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241385.1","gene_symbol":"AC023245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109899246,"end":109899762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231637.3","gene_symbol":"USP17L29","gene_name":"ubiquitin specific peptidase 17-like family member 29 [Source:HGNC Symbol;Acc:HGNC:44457]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728405","summary":null,"start":9353638,"end":9355230,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 29 [Source:HGNC Symbol;Acc:HGNC:44457]"}, {"versioned_ensembl_gene_id":"ENSG00000273265.1","gene_symbol":"AC092636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96812239,"end":96813657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251694.1","gene_symbol":"USP17L9P","gene_name":"ubiquitin specific peptidase 17-like family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:12615]","synonyms":"USP17,RS447","biotype":"unprocessed_pseudogene","ncbi_id":"391627","summary":null,"start":9358383,"end":9359975,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:12615]"}, {"versioned_ensembl_gene_id":"ENSG00000228856.3","gene_symbol":"USP17L30","gene_name":"ubiquitin specific peptidase 17-like family member 30 [Source:HGNC Symbol;Acc:HGNC:44458]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728419","summary":null,"start":9363129,"end":9364721,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 30 [Source:HGNC Symbol;Acc:HGNC:44458]"}, {"versioned_ensembl_gene_id":"ENSG00000164794.8","gene_symbol":"KCNV1","gene_name":"potassium voltage-gated channel modifier subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:18861]","synonyms":"Kv8.1","biotype":"protein_coding","ncbi_id":"27012","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium voltage-gated channel subfamily V. This protein is essentially present in the brain, and its role might be to inhibit the function of a particular class of outward rectifier potassium channel types. [provided by RefSeq, Jul 2008]","start":109963645,"end":109975847,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:18861]"}, {"versioned_ensembl_gene_id":"ENSG00000117010.15","gene_symbol":"ZNF684","gene_name":"zinc finger protein 684 [Source:HGNC Symbol;Acc:HGNC:28418]","synonyms":"MGC27466","biotype":"protein_coding","ncbi_id":"127396","summary":null,"start":40531561,"end":40548169,"strand":1,"description":"zinc finger protein 684 [Source:HGNC Symbol;Acc:HGNC:28418]"}, {"versioned_ensembl_gene_id":"ENSG00000243664.1","gene_symbol":"RPS29P12","gene_name":"ribosomal protein S29 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36458]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131173","summary":null,"start":180945756,"end":180945907,"strand":1,"description":"ribosomal protein S29 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36458]"}, {"versioned_ensembl_gene_id":"ENSG00000259362.2","gene_symbol":"AC046168.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77525540,"end":77534110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258856.2","gene_symbol":"AL136520.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":57629841,"end":57631162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248761.1","gene_symbol":"AC091874.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180967848,"end":180968567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249287.1","gene_symbol":"AC091874.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180967189,"end":180970762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213110.2","gene_symbol":"AC019178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189930277,"end":189931010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255347.1","gene_symbol":"AC021820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40083710,"end":40084517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255402.1","gene_symbol":"AC027451.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109973943,"end":109974781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259039.1","gene_symbol":"AL161804.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57578632,"end":57581320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204253.4","gene_symbol":"HNRNPCP2","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48814]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653447","summary":null,"start":189923336,"end":189924216,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48814]"}, {"versioned_ensembl_gene_id":"ENSG00000231228.4","gene_symbol":"AC091874.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180982273,"end":180982611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240590.1","gene_symbol":"RPSAP48","gene_name":"ribosomal protein SA pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392262","summary":null,"start":110105076,"end":110105964,"strand":-1,"description":"ribosomal protein SA pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36646]"}, {"versioned_ensembl_gene_id":"ENSG00000234569.1","gene_symbol":"RAD1P1","gene_name":"RAD1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49479]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128880","summary":null,"start":119621068,"end":119621880,"strand":1,"description":"RAD1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49479]"}, {"versioned_ensembl_gene_id":"ENSG00000225579.1","gene_symbol":"EDNRB-AS1","gene_name":"EDNRB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49045]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505518","summary":null,"start":77828222,"end":77833950,"strand":1,"description":"EDNRB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49045]"}, {"versioned_ensembl_gene_id":"ENSG00000227437.1","gene_symbol":"RPS8P4","gene_name":"ribosomal protein S8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:17478]","synonyms":"Em:AC012468.5","biotype":"processed_pseudogene","ncbi_id":"646119","summary":null,"start":119638456,"end":119639082,"strand":1,"description":"ribosomal protein S8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:17478]"}, {"versioned_ensembl_gene_id":"ENSG00000183598.3","gene_symbol":"HIST2H3D","gene_name":"histone cluster 2 H3 family member d [Source:HGNC Symbol;Acc:HGNC:25311]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653604","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. [provided by RefSeq, Aug 2015]","start":149813271,"end":149813681,"strand":-1,"description":"histone cluster 2 H3 family member d [Source:HGNC Symbol;Acc:HGNC:25311]"}, {"versioned_ensembl_gene_id":"ENSG00000145217.13","gene_symbol":"SLC26A1","gene_name":"solute carrier family 26 member 1 [Source:HGNC Symbol;Acc:HGNC:10993]","synonyms":"SAT-1,EDM4","biotype":"protein_coding","ncbi_id":"10861","summary":"This gene is a member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures, but have markedly different tissue expression patterns. This gene is primarily expressed in the liver, pancreas, and brain. Three splice variants that encode different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":979073,"end":993440,"strand":-1,"description":"solute carrier family 26 member 1 [Source:HGNC Symbol;Acc:HGNC:10993]"}, {"versioned_ensembl_gene_id":"ENSG00000141012.12","gene_symbol":"GALNS","gene_name":"galactosamine (N-acetyl)-6-sulfatase [Source:HGNC Symbol;Acc:HGNC:4122]","synonyms":"GALNAC6S,GAS","biotype":"protein_coding","ncbi_id":"2588","summary":"This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder. [provided by RefSeq, Jul 2008]","start":88813734,"end":88856970,"strand":-1,"description":"galactosamine (N-acetyl)-6-sulfatase [Source:HGNC Symbol;Acc:HGNC:4122]"}, {"versioned_ensembl_gene_id":"ENSG00000105464.3","gene_symbol":"GRIN2D","gene_name":"glutamate ionotropic receptor NMDA type subunit 2D [Source:HGNC Symbol;Acc:HGNC:4588]","synonyms":"NR2D,NMDAR2D,GluN2D,EB11","biotype":"protein_coding","ncbi_id":"2906","summary":"N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. NMDA channel has been shown to be involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDA receptor channels are heteromers composed of the key receptor subunit NMDAR1 (GRIN1) and 1 or more of the 4 NMDAR2 subunits: NMDAR2A (GRIN2A), NMDAR2B (GRIN2B), NMDAR2C (GRIN2C), and NMDAR2D (GRIN2D). [provided by RefSeq, Mar 2010]","start":48394875,"end":48444931,"strand":1,"description":"glutamate ionotropic receptor NMDA type subunit 2D [Source:HGNC Symbol;Acc:HGNC:4588]"}, {"versioned_ensembl_gene_id":"ENSG00000203811.1","gene_symbol":"HIST2H3C","gene_name":"histone cluster 2 H3 family member c [Source:HGNC Symbol;Acc:HGNC:20503]","synonyms":"MGC9629,H3FM,H3F2,H3/m,H3.2,H3","biotype":"protein_coding","ncbi_id":"126961","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the telomeric copy. [provided by RefSeq, Aug 2015]","start":149839538,"end":149841193,"strand":-1,"description":"histone cluster 2 H3 family member c [Source:HGNC Symbol;Acc:HGNC:20503]"}, {"versioned_ensembl_gene_id":"ENSG00000115966.16","gene_symbol":"ATF2","gene_name":"activating transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:784]","synonyms":"TREB7,HB16,CREB2,CRE-BP1","biotype":"protein_coding","ncbi_id":"1386","summary":"This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions This protein binds to the cAMP-responsive element (CRE), an octameric palindrome. It forms a homodimer or a heterodimer with c-Jun and stimulates CRE-dependent transcription. This protein is also a histone acetyltransferase (HAT) that specifically acetylates histones H2B and H4 in vitro; thus it may represent a class of sequence-specific factors that activate transcription by direct effects on chromatin components. The encoded protein may also be involved in cell's DNA damage response independent of its role in transcriptional regulation. Several alternatively spliced transcript variants have been found for this gene [provided by RefSeq, Jan 2014]","start":175072250,"end":175168382,"strand":-1,"description":"activating transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:784]"}, {"versioned_ensembl_gene_id":"ENSG00000270882.2","gene_symbol":"HIST2H4A","gene_name":"histone cluster 2 H4 family member a [Source:HGNC Symbol;Acc:HGNC:4794]","synonyms":"HIST2H4,H4FN,H4F2,H4/n","biotype":"protein_coding","ncbi_id":"8370","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the centromeric copy. [provided by RefSeq, Aug 2015]","start":149832659,"end":149839767,"strand":1,"description":"histone cluster 2 H4 family member a [Source:HGNC Symbol;Acc:HGNC:4794]"}, {"versioned_ensembl_gene_id":"ENSG00000205946.1","gene_symbol":"USP17L6P","gene_name":"ubiquitin specific peptidase 17-like family member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37179]","synonyms":"vDUB4,USP17L6,DUB4","biotype":"unprocessed_pseudogene","ncbi_id":"391622","summary":null,"start":9367874,"end":9369070,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:37179]"}, {"versioned_ensembl_gene_id":"ENSG00000135069.13","gene_symbol":"PSAT1","gene_name":"phosphoserine aminotransferase 1 [Source:HGNC Symbol;Acc:HGNC:19129]","synonyms":"PSA","biotype":"protein_coding","ncbi_id":"29968","summary":"This gene encodes a member of the class-V pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is a phosphoserine aminotransferase and decreased expression may be associated with schizophrenia. Mutations in this gene are also associated with phosphoserine aminotransferase deficiency. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 1, 3, and 8. [provided by RefSeq, Jul 2013]","start":78297143,"end":78330093,"strand":1,"description":"phosphoserine aminotransferase 1 [Source:HGNC Symbol;Acc:HGNC:19129]"}, {"versioned_ensembl_gene_id":"ENSG00000279675.1","gene_symbol":"AC080100.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40107244,"end":40112599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219492.4","gene_symbol":"AC116655.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9384017,"end":9388983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182968.4","gene_symbol":"SOX1","gene_name":"SRY-box 1 [Source:HGNC Symbol;Acc:HGNC:11189]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6656","summary":"This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. In mice, a similar protein regulates the gamma-crystallin genes and is essential for lens development. [provided by RefSeq, Jul 2008]","start":112067647,"end":112070488,"strand":1,"description":"SRY-box 1 [Source:HGNC Symbol;Acc:HGNC:11189]"}, {"versioned_ensembl_gene_id":"ENSG00000261672.1","gene_symbol":"AC079789.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173593672,"end":173594556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214076.3","gene_symbol":"CPSF1P1","gene_name":"cleavage and polyadenylation specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19251]","synonyms":"dJ90G24.5","biotype":"processed_pseudogene","ncbi_id":"129099","summary":null,"start":32269381,"end":32273110,"strand":1,"description":"cleavage and polyadenylation specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19251]"}, {"versioned_ensembl_gene_id":"ENSG00000224141.5","gene_symbol":"MIR548XHG","gene_name":"MIR548X host gene [Source:HGNC Symbol;Acc:HGNC:52006]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927797","summary":null,"start":18561265,"end":18760003,"strand":-1,"description":"MIR548X host gene [Source:HGNC Symbol;Acc:HGNC:52006]"}, {"versioned_ensembl_gene_id":"ENSG00000145214.13","gene_symbol":"DGKQ","gene_name":"diacylglycerol kinase theta [Source:HGNC Symbol;Acc:HGNC:2856]","synonyms":"DAGK7,DAGK4,DAGK","biotype":"protein_coding","ncbi_id":"1609","summary":"The protein encoded by this gene contains three cysteine-rich domains, a proline-rich region, and a pleckstrin homology domain with an overlapping Ras-associating domain. It is localized in the speckle domains of the nucleus, and mediates the regeneration of phosphatidylinositol (PI) from diacylglycerol in the PI-cycle during cell signal transduction. [provided by RefSeq, Jul 2008]","start":958887,"end":986895,"strand":-1,"description":"diacylglycerol kinase theta [Source:HGNC Symbol;Acc:HGNC:2856]"}, {"versioned_ensembl_gene_id":"ENSG00000230120.1","gene_symbol":"AL008723.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32159454,"end":32160392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172023.7","gene_symbol":"REG1B","gene_name":"regenerating family member 1 beta [Source:HGNC Symbol;Acc:HGNC:9952]","synonyms":"REGL,REGI-BETA,REGH,PSPS2","biotype":"protein_coding","ncbi_id":"5968","summary":"This gene is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. This gene encodes a protein secreted by the exocrine pancreas that is highly similar to the REG1A protein. The related REG1A protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic lithogenesis. Reg family members REG1A, REGL, PAP and this gene are tandemly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication. [provided by RefSeq, Jul 2008]","start":79085030,"end":79088019,"strand":-1,"description":"regenerating family member 1 beta [Source:HGNC Symbol;Acc:HGNC:9952]"}, {"versioned_ensembl_gene_id":"ENSG00000226114.1","gene_symbol":"NDUFB4P5","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45253]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075096","summary":null,"start":86934462,"end":86934822,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45253]"}, {"versioned_ensembl_gene_id":"ENSG00000234171.2","gene_symbol":"RNASEH1-AS1","gene_name":"RNASEH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49289]","synonyms":"LOC100506054","biotype":"antisense_RNA","ncbi_id":"100506054","summary":null,"start":3558492,"end":3561745,"strand":1,"description":"RNASEH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49289]"}, {"versioned_ensembl_gene_id":"ENSG00000112081.16","gene_symbol":"SRSF3","gene_name":"serine and arginine rich splicing factor 3 [Source:HGNC Symbol;Acc:HGNC:10785]","synonyms":"SRp20,SFRS3","biotype":"protein_coding","ncbi_id":"6428","summary":"The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two transcript variants, one protein-coding and the other non-coding, have been found for this gene. [provided by RefSeq, Sep 2010]","start":36594353,"end":36605600,"strand":1,"description":"serine and arginine rich splicing factor 3 [Source:HGNC Symbol;Acc:HGNC:10785]"}, {"versioned_ensembl_gene_id":"ENSG00000233673.7","gene_symbol":"ANAPC1P1","gene_name":"anaphase promoting complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44150]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100286979","summary":null,"start":86861825,"end":86912978,"strand":1,"description":"anaphase promoting complex subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44150]"}, {"versioned_ensembl_gene_id":"ENSG00000214560.4","gene_symbol":"RPL21P41","gene_name":"ribosomal protein L21 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271159","summary":null,"start":66637149,"end":66637412,"strand":1,"description":"ribosomal protein L21 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36765]"}, {"versioned_ensembl_gene_id":"ENSG00000163126.14","gene_symbol":"ANKRD23","gene_name":"ankyrin repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:24470]","synonyms":"MARP3,FLJ32449,DARP","biotype":"protein_coding","ncbi_id":"200539","summary":"This gene is a member of the muscle ankyrin repeat protein (MARP) family and encodes a protein with four tandem ankyrin-like repeats. The protein is localized to the nucleus, functioning as a transcriptional regulator. Expression of this protein is induced during recovery following starvation. [provided by RefSeq, Jul 2008]","start":96824526,"end":96857934,"strand":-1,"description":"ankyrin repeat domain 23 [Source:HGNC Symbol;Acc:HGNC:24470]"}, {"versioned_ensembl_gene_id":"ENSG00000165810.16","gene_symbol":"BTNL9","gene_name":"butyrophilin like 9 [Source:HGNC Symbol;Acc:HGNC:24176]","synonyms":"FLJ32535,BTN8","biotype":"protein_coding","ncbi_id":"153579","summary":null,"start":181040225,"end":181061523,"strand":1,"description":"butyrophilin like 9 [Source:HGNC Symbol;Acc:HGNC:24176]"}, {"versioned_ensembl_gene_id":"ENSG00000254127.1","gene_symbol":"IGLCOR22-1","gene_name":"immunoglobulin lambda constant/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15696]","synonyms":"IGLC/OR22-1","biotype":"IG_C_pseudogene","ncbi_id":"84096","summary":null,"start":32199919,"end":32200234,"strand":1,"description":"immunoglobulin lambda constant/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15696]"}, {"versioned_ensembl_gene_id":"ENSG00000234021.1","gene_symbol":"AL596451.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8936079,"end":8963077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212829.8","gene_symbol":"RPS26P3","gene_name":"ribosomal protein S26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23411]","synonyms":"bA338L20.1","biotype":"processed_pseudogene","ncbi_id":"441386","summary":null,"start":9090898,"end":9091245,"strand":1,"description":"ribosomal protein S26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23411]"}, {"versioned_ensembl_gene_id":"ENSG00000128253.13","gene_symbol":"RFPL2","gene_name":"ret finger protein like 2 [Source:HGNC Symbol;Acc:HGNC:9979]","synonyms":"RNF79","biotype":"protein_coding","ncbi_id":"10739","summary":null,"start":32190435,"end":32203477,"strand":-1,"description":"ret finger protein like 2 [Source:HGNC Symbol;Acc:HGNC:9979]"}, {"versioned_ensembl_gene_id":"ENSG00000260385.1","gene_symbol":"AL356961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112083549,"end":112085471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234360.1","gene_symbol":"AL135790.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10532145,"end":10532411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276146.4","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"LIR-2,MIR10,ILT4,MIR-10,CD85d,LIR2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54274195,"end":54281689,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000263677.1","gene_symbol":"AC012588.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26688111,"end":26689668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230920.1","gene_symbol":"AL513422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9799423,"end":9803784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265369.3","gene_symbol":"PCAT18","gene_name":"prostate cancer associated transcript 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49211]","synonyms":"LINC01092","biotype":"lincRNA","ncbi_id":"728606","summary":null,"start":26687621,"end":26703638,"strand":-1,"description":"prostate cancer associated transcript 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49211]"}, {"versioned_ensembl_gene_id":"ENSG00000128594.7","gene_symbol":"LRRC4","gene_name":"leucine rich repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:15586]","synonyms":"NAG14","biotype":"protein_coding","ncbi_id":"64101","summary":"This gene is significantly downregulated in primary brain tumors. The exact function of the protein encoded by this gene is unknown. [provided by RefSeq, Jul 2008]","start":128027071,"end":128032107,"strand":-1,"description":"leucine rich repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:15586]"}, {"versioned_ensembl_gene_id":"ENSG00000277534.1","gene_symbol":"AC007996.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26542971,"end":26545791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225706.1","gene_symbol":"PTPRD-AS1","gene_name":"PTPRD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49753]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929407","summary":null,"start":8858130,"end":8862255,"strand":1,"description":"PTPRD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49753]"}, {"versioned_ensembl_gene_id":"ENSG00000146378.6","gene_symbol":"TAAR2","gene_name":"trace amine associated receptor 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4514]","synonyms":"GPR58","biotype":"protein_coding","ncbi_id":"9287","summary":null,"start":132617022,"end":132624275,"strand":-1,"description":"trace amine associated receptor 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4514]"}, {"versioned_ensembl_gene_id":"ENSG00000134504.12","gene_symbol":"KCTD1","gene_name":"potassium channel tetramerization domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18249]","synonyms":"C18orf5","biotype":"protein_coding","ncbi_id":"284252","summary":"This gene encodes a protein containing a BTB (Broad-complex, tramtrack and bric a brac), also known as a POZ (POxvirus and zinc finger) protein-protein interaction domain. The encoded protein negatively regulates the AP-2 family of transcription factors and the Wnt signaling pathway. A mechanism for the modulation of Wnt signaling has been proposed in which the encoded protein enhances ubiquitination and degradation of the beta-catenin protein. Mutations in this gene have been identified in Scalp-ear-nipple (SEN) syndrome. [provided by RefSeq, May 2017]","start":26454910,"end":26657401,"strand":-1,"description":"potassium channel tetramerization domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18249]"}, {"versioned_ensembl_gene_id":"ENSG00000188438.4","gene_symbol":"DEFB108F","gene_name":"defensin beta 108F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38062]","synonyms":"DEFB108P5","biotype":"unprocessed_pseudogene","ncbi_id":"100133128","summary":null,"start":9399204,"end":9403565,"strand":1,"description":"defensin beta 108F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38062]"}, {"versioned_ensembl_gene_id":"ENSG00000243725.6","gene_symbol":"TTC4","gene_name":"tetratricopeptide repeat domain 4 [Source:HGNC Symbol;Acc:HGNC:12394]","synonyms":"MGC5097,FLJ41930,CNS1","biotype":"protein_coding","ncbi_id":"7268","summary":"This gene encodes a protein that contains tetratricopeptide (TPR) repeats, which often mediate protein-protein interactions and chaperone activity. The encoded protein interacts with heat shock proteins 70 and 90. Alternative splicing results in multiple transcript variants. Naturally-occuring readthrough transcription occurs from upstream gene MROH (maestro heat-like repeat family member 7) to this gene. [provided by RefSeq, Apr 2014]","start":54715822,"end":54742657,"strand":1,"description":"tetratricopeptide repeat domain 4 [Source:HGNC Symbol;Acc:HGNC:12394]"}, {"versioned_ensembl_gene_id":"ENSG00000232773.2","gene_symbol":"DEFB130D","gene_name":"defensin beta 130D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38059]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9422313,"end":9429702,"strand":1,"description":"defensin beta 130D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38059]"}, {"versioned_ensembl_gene_id":"ENSG00000279078.1","gene_symbol":"SND1-IT1","gene_name":"SND1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:24158]","synonyms":"NSG-X,NAG8,C7orf54","biotype":"lincRNA","ncbi_id":"27099","summary":null,"start":127997597,"end":128000077,"strand":1,"description":"SND1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:24158]"}, {"versioned_ensembl_gene_id":"ENSG00000153707.16","gene_symbol":"PTPRD","gene_name":"protein tyrosine phosphatase, receptor type D [Source:HGNC Symbol;Acc:HGNC:9668]","synonyms":"PTPD,HPTP","biotype":"protein_coding","ncbi_id":"5789","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular region, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this protein is composed of three Ig-like and eight fibronectin type III-like domains. Studies of the similar genes in chicken and fly suggest the role of this PTP is in promoting neurite growth, and regulating neurons axon guidance. Multiple alternatively spliced transcript variants of this gene have been reported. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jan 2010]","start":8314246,"end":10612723,"strand":-1,"description":"protein tyrosine phosphatase, receptor type D [Source:HGNC Symbol;Acc:HGNC:9668]"}, {"versioned_ensembl_gene_id":"ENSG00000184194.5","gene_symbol":"GPR173","gene_name":"G protein-coupled receptor 173 [Source:HGNC Symbol;Acc:HGNC:18186]","synonyms":"SREB3","biotype":"protein_coding","ncbi_id":"54328","summary":"This gene encodes a member of the G-protein coupled receptor 1 family. This protein contains 7 transmembrane domains and conserved cysteine residues. [provided by RefSeq, Nov 2009]","start":53049091,"end":53080615,"strand":1,"description":"G protein-coupled receptor 173 [Source:HGNC Symbol;Acc:HGNC:18186]"}, {"versioned_ensembl_gene_id":"ENSG00000255767.1","gene_symbol":"AC108488.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3531984,"end":3547957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187627.15","gene_symbol":"RGPD1","gene_name":"RANBP2-like and GRIP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32414]","synonyms":"RGP1","biotype":"protein_coding","ncbi_id":"400966","summary":null,"start":86907953,"end":87013976,"strand":1,"description":"RANBP2-like and GRIP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32414]"}, {"versioned_ensembl_gene_id":"ENSG00000136870.10","gene_symbol":"ZNF189","gene_name":"zinc finger protein 189 [Source:HGNC Symbol;Acc:HGNC:12980]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7743","summary":"Kruppel-like zinc finger proteins such as ZNF189 contain a conserved stretch of 7 amino acids that connects a variable number of DNA-binding zinc finger repeats of the cys(2)his(2) (C2H2) type (summarized by Odeberg et al., 1998 [PubMed 9653648]). Approximately 30% of human Kruppel-like zinc finger proteins contain an N-terminal Kruppel-associated box (KRAB) domain. The KRAB domain consists of approximately 75 amino acids that may be subdivided into an A box, which is present in every KRAB domain and is essential for transcriptional repression, and a B box, which is not always present.[supplied by OMIM, May 2010]","start":101398873,"end":101410660,"strand":1,"description":"zinc finger protein 189 [Source:HGNC Symbol;Acc:HGNC:12980]"}, {"versioned_ensembl_gene_id":"ENSG00000187492.8","gene_symbol":"CDHR4","gene_name":"cadherin related family member 4 [Source:HGNC Symbol;Acc:HGNC:34527]","synonyms":"VLLR9392,CDH29","biotype":"protein_coding","ncbi_id":"389118","summary":null,"start":49790732,"end":49799835,"strand":-1,"description":"cadherin related family member 4 [Source:HGNC Symbol;Acc:HGNC:34527]"}, {"versioned_ensembl_gene_id":"ENSG00000270497.1","gene_symbol":"BX322635.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53065053,"end":53065548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171865.9","gene_symbol":"RNASEH1","gene_name":"ribonuclease H1 [Source:HGNC Symbol;Acc:HGNC:18466]","synonyms":null,"biotype":"protein_coding","ncbi_id":"246243","summary":"This gene encodes an endonuclease that specifically degrades the RNA of RNA-DNA hybrids and plays a key role in DNA replication and repair. Alternate in-frame start codon initiation results in the production of alternate isoforms that are directed to the mitochondria or to the nucleus. The production of the mitochondrial isoform is modulated by an upstream open reading frame (uORF). Mutations in this gene have been found in individuals with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2. Alternative splicing results in additional coding and non-coding transcript variants. Pseudogenes of this gene have been defined on chromosomes 2 and 17. [provided by RefSeq, Jul 2017]","start":3544793,"end":3558616,"strand":-1,"description":"ribonuclease H1 [Source:HGNC Symbol;Acc:HGNC:18466]"}, {"versioned_ensembl_gene_id":"ENSG00000268465.1","gene_symbol":"AC008403.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":48465837,"end":48472431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184313.19","gene_symbol":"MROH7","gene_name":"maestro heat like repeat family member 7 [Source:HGNC Symbol;Acc:HGNC:24802]","synonyms":"C1orf175,HEATR8,FLJ46354","biotype":"protein_coding","ncbi_id":"374977","summary":null,"start":54641754,"end":54710266,"strand":1,"description":"maestro heat like repeat family member 7 [Source:HGNC Symbol;Acc:HGNC:24802]"}, {"versioned_ensembl_gene_id":"ENSG00000087237.10","gene_symbol":"CETP","gene_name":"cholesteryl ester transfer protein [Source:HGNC Symbol;Acc:HGNC:1869]","synonyms":"BPIFF","biotype":"protein_coding","ncbi_id":"1071","summary":"The protein encoded by this gene is found in plasma, where it is involved in the transfer of cholesteryl ester from high density lipoprotein (HDL) to other lipoproteins. Defects in this gene are a cause of hyperalphalipoproteinemia 1 (HALP1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":56961850,"end":56983845,"strand":1,"description":"cholesteryl ester transfer protein [Source:HGNC Symbol;Acc:HGNC:1869]"}, {"versioned_ensembl_gene_id":"ENSG00000139531.12","gene_symbol":"SUOX","gene_name":"sulfite oxidase [Source:HGNC Symbol;Acc:HGNC:11460]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6821","summary":"Sulfite oxidase is a homodimeric protein localized to the intermembrane space of mitochondria. Each subunit contains a heme domain and a molybdopterin-binding domain. The enzyme catalyzes the oxidation of sulfite to sulfate, the final reaction in the oxidative degradation of the sulfur amino acids cysteine and methionine. Sulfite oxidase deficiency results in neurological abnormalities which are often fatal at an early age. Alternative splicing results in multiple transcript variants encoding identical proteins. [provided by RefSeq, Jul 2008]","start":55997180,"end":56006641,"strand":1,"description":"sulfite oxidase [Source:HGNC Symbol;Acc:HGNC:11460]"}, {"versioned_ensembl_gene_id":"ENSG00000235449.2","gene_symbol":"AC098934.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202767229,"end":202767418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155368.16","gene_symbol":"DBI","gene_name":"diazepam binding inhibitor, acyl-CoA binding protein [Source:HGNC Symbol;Acc:HGNC:2690]","synonyms":"ACBP,ACBD1","biotype":"protein_coding","ncbi_id":"1622","summary":"This gene encodes diazepam binding inhibitor, a protein that is regulated by hormones and is involved in lipid metabolism and the displacement of beta-carbolines and benzodiazepines, which modulate signal transduction at type A gamma-aminobutyric acid receptors located in brain synapses. The protein is conserved from yeast to mammals, with the most highly conserved domain consisting of seven contiguous residues that constitute the hydrophobic binding site for medium- and long-chain acyl-Coenzyme A esters. Diazepam binding inhibitor is also known to mediate the feedback regulation of pancreatic secretion and the postprandial release of cholecystokinin, in addition to its role as a mediator in corticotropin-dependent adrenal steroidogenesis. Three pseudogenes located on chromosomes 6, 8 and 16 have been identified. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":119366921,"end":119372560,"strand":1,"description":"diazepam binding inhibitor, acyl-CoA binding protein [Source:HGNC Symbol;Acc:HGNC:2690]"}, {"versioned_ensembl_gene_id":"ENSG00000241870.1","gene_symbol":"AC008620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181065086,"end":181065677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105443.14","gene_symbol":"CYTH2","gene_name":"cytohesin 2 [Source:HGNC Symbol;Acc:HGNC:9502]","synonyms":"Sec7p-L,PSCD2L,PSCD2,cytohesin-2,CTS18.1,ARNO,Sec7p-like","biotype":"protein_coding","ncbi_id":"9266","summary":"The protein encoded by this gene is a member of the PSCD family. Members of this family have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. The encoded protein exhibits GEP activity in vitro with ARF1, ARF3, and ARF6 and is 83% homologous to CYTH1. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":48469032,"end":48482314,"strand":1,"description":"cytohesin 2 [Source:HGNC Symbol;Acc:HGNC:9502]"}, {"versioned_ensembl_gene_id":"ENSG00000214295.4","gene_symbol":"FOXO1B","gene_name":"forkhead box O1B pseudogene [Source:HGNC Symbol;Acc:HGNC:3820]","synonyms":"FKHRP1","biotype":"processed_pseudogene","ncbi_id":"2311","summary":null,"start":181099140,"end":181100666,"strand":-1,"description":"forkhead box O1B pseudogene [Source:HGNC Symbol;Acc:HGNC:3820]"}, {"versioned_ensembl_gene_id":"ENSG00000248560.1","gene_symbol":"AC008620.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181114106,"end":181115674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174899.10","gene_symbol":"PQLC2L","gene_name":"PQ loop repeat containing 2 like [Source:HGNC Symbol;Acc:HGNC:25146]","synonyms":"C3orf55","biotype":"protein_coding","ncbi_id":"152078","summary":null,"start":157543246,"end":157677749,"strand":1,"description":"PQ loop repeat containing 2 like [Source:HGNC Symbol;Acc:HGNC:25146]"}, {"versioned_ensembl_gene_id":"ENSG00000257105.1","gene_symbol":"AC006581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8987175,"end":8996566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185372.3","gene_symbol":"OR2V1","gene_name":"olfactory receptor family 2 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:8280]","synonyms":"OST265,OR2V1P","biotype":"protein_coding","ncbi_id":"26693","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":181123122,"end":181131169,"strand":-1,"description":"olfactory receptor family 2 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:8280]"}, {"versioned_ensembl_gene_id":"ENSG00000139187.9","gene_symbol":"KLRG1","gene_name":"killer cell lectin like receptor G1 [Source:HGNC Symbol;Acc:HGNC:6380]","synonyms":"MAFA-L,MAFA,CLEC15A,2F1","biotype":"protein_coding","ncbi_id":"10219","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. The protein encoded by this gene belongs to the killer cell lectin-like receptor (KLR) family, which is a group of transmembrane proteins preferentially expressed in NK cells. Studies in mice suggested that the expression of this gene may be regulated by MHC class I molecules. [provided by RefSeq, Jun 2016]","start":8950044,"end":9010760,"strand":1,"description":"killer cell lectin like receptor G1 [Source:HGNC Symbol;Acc:HGNC:6380]"}, {"versioned_ensembl_gene_id":"ENSG00000198182.12","gene_symbol":"ZNF607","gene_name":"zinc finger protein 607 [Source:HGNC Symbol;Acc:HGNC:28192]","synonyms":"MGC13071,FLJ14802","biotype":"protein_coding","ncbi_id":"84775","summary":null,"start":37696363,"end":37719790,"strand":-1,"description":"zinc finger protein 607 [Source:HGNC Symbol;Acc:HGNC:28192]"}, {"versioned_ensembl_gene_id":"ENSG00000182613.2","gene_symbol":"OR2V2","gene_name":"olfactory receptor family 2 subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:15341]","synonyms":"OST713,OR2V3","biotype":"protein_coding","ncbi_id":"285659","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":181147586,"end":181159285,"strand":1,"description":"olfactory receptor family 2 subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:15341]"}, {"versioned_ensembl_gene_id":"ENSG00000168763.15","gene_symbol":"CNNM3","gene_name":"cyclin and CBS domain divalent metal cation transport mediator 3 [Source:HGNC Symbol;Acc:HGNC:104]","synonyms":"ACDP3","biotype":"protein_coding","ncbi_id":"26505","summary":null,"start":96816245,"end":96833911,"strand":1,"description":"cyclin and CBS domain divalent metal cation transport mediator 3 [Source:HGNC Symbol;Acc:HGNC:104]"}, {"versioned_ensembl_gene_id":"ENSG00000248473.1","gene_symbol":"LINC01962","gene_name":"long intergenic non-protein coding RNA 1962 [Source:HGNC Symbol;Acc:HGNC:52787]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102577426","summary":null,"start":181191046,"end":181191852,"strand":-1,"description":"long intergenic non-protein coding RNA 1962 [Source:HGNC Symbol;Acc:HGNC:52787]"}, {"versioned_ensembl_gene_id":"ENSG00000134884.13","gene_symbol":"ARGLU1","gene_name":"arginine and glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:25482]","synonyms":"FLJ10154","biotype":"protein_coding","ncbi_id":"55082","summary":null,"start":106541673,"end":106568164,"strand":-1,"description":"arginine and glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:25482]"}, {"versioned_ensembl_gene_id":"ENSG00000134571.10","gene_symbol":"MYBPC3","gene_name":"myosin binding protein C, cardiac [Source:HGNC Symbol;Acc:HGNC:7551]","synonyms":"MYBP-C,FHC,CMH4","biotype":"protein_coding","ncbi_id":"4607","summary":"MYBPC3 encodes the cardiac isoform of myosin-binding protein C. Myosin-binding protein C is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. MYBPC3, the cardiac isoform, is expressed exclussively in heart muscle. Regulatory phosphorylation of the cardiac isoform in vivo by cAMP-dependent protein kinase (PKA) upon adrenergic stimulation may be linked to modulation of cardiac contraction. Mutations in MYBPC3 are one cause of familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]","start":47331397,"end":47352702,"strand":-1,"description":"myosin binding protein C, cardiac [Source:HGNC Symbol;Acc:HGNC:7551]"}, {"versioned_ensembl_gene_id":"ENSG00000236222.8","gene_symbol":"WDR46","gene_name":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]","synonyms":"BING4,UTP7,C6orf11","biotype":"protein_coding","ncbi_id":"9277","summary":null,"start":33449481,"end":33459870,"strand":-1,"description":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]"}, {"versioned_ensembl_gene_id":"ENSG00000259601.2","gene_symbol":"AC092079.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59871511,"end":59873495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261818.1","gene_symbol":"AC092138.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65580668,"end":65646947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127415.12","gene_symbol":"IDUA","gene_name":"iduronidase, alpha-L- [Source:HGNC Symbol;Acc:HGNC:5391]","synonyms":"MPS1","biotype":"protein_coding","ncbi_id":"3425","summary":"This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). [provided by RefSeq, Jul 2008]","start":986997,"end":1004506,"strand":1,"description":"iduronidase, alpha-L- [Source:HGNC Symbol;Acc:HGNC:5391]"}, {"versioned_ensembl_gene_id":"ENSG00000117139.16","gene_symbol":"KDM5B","gene_name":"lysine demethylase 5B [Source:HGNC Symbol;Acc:HGNC:18039]","synonyms":"RBBP2H1A,PPP1R98,PLU-1,JARID1B,CT31","biotype":"protein_coding","ncbi_id":"10765","summary":"This gene encodes a lysine-specific histone demethylase that belongs to the jumonji/ARID domain-containing family of histone demethylases. The encoded protein is capable of demethylating tri-, di- and monomethylated lysine 4 of histone H3. This protein plays a role in the transcriptional repression or certain tumor suppressor genes and is upregulated in certain cancer cells. This protein may also play a role in genome stability and DNA repair. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":202724491,"end":202809470,"strand":-1,"description":"lysine demethylase 5B [Source:HGNC Symbol;Acc:HGNC:18039]"}, {"versioned_ensembl_gene_id":"ENSG00000253572.2","gene_symbol":"AC108482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77942757,"end":77946438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255236.2","gene_symbol":"AP002992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68122053,"end":68130518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257759.2","gene_symbol":"AL357153.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70425812,"end":70547464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171817.16","gene_symbol":"ZNF540","gene_name":"zinc finger protein 540 [Source:HGNC Symbol;Acc:HGNC:25331]","synonyms":"DKFZp547B0714","biotype":"protein_coding","ncbi_id":"163255","summary":null,"start":37551406,"end":37614097,"strand":1,"description":"zinc finger protein 540 [Source:HGNC Symbol;Acc:HGNC:25331]"}, {"versioned_ensembl_gene_id":"ENSG00000134007.3","gene_symbol":"ADAM20","gene_name":"ADAM metallopeptidase domain 20 [Source:HGNC Symbol;Acc:HGNC:199]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8748","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The expression of this gene is testis-specific. [provided by RefSeq, Jul 2008]","start":70522358,"end":70535015,"strand":-1,"description":"ADAM metallopeptidase domain 20 [Source:HGNC Symbol;Acc:HGNC:199]"}, {"versioned_ensembl_gene_id":"ENSG00000146385.1","gene_symbol":"TAAR8","gene_name":"trace amine associated receptor 8 [Source:HGNC Symbol;Acc:HGNC:14964]","synonyms":"TRAR5,TAR5,TA5,GPR102","biotype":"protein_coding","ncbi_id":"83551","summary":"This gene is part of the trace amine receptor cluster on chromosome 6 and encodes an orphan G-protein coupled receptor. Upregulated expression of this gene in astroglial cells upon exposure to lipopolysaccharides suggests a function for the encoded protein in the brain. [provided by RefSeq, Jul 2016]","start":132552693,"end":132553721,"strand":1,"description":"trace amine associated receptor 8 [Source:HGNC Symbol;Acc:HGNC:14964]"}, {"versioned_ensembl_gene_id":"ENSG00000146054.17","gene_symbol":"TRIM7","gene_name":"tripartite motif containing 7 [Source:HGNC Symbol;Acc:HGNC:16278]","synonyms":"RNF90,GNIP","biotype":"protein_coding","ncbi_id":"81786","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1, a B-box type 2, and a coiled-coil region. The protein localizes to both the nucleus and the cytoplasm, and may represent a participant in the initiation of glycogen synthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":181193924,"end":181205293,"strand":-1,"description":"tripartite motif containing 7 [Source:HGNC Symbol;Acc:HGNC:16278]"}, {"versioned_ensembl_gene_id":"ENSG00000235998.1","gene_symbol":"TAAR7P","gene_name":"trace amine associated receptor 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31925]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"503611","summary":null,"start":132559024,"end":132559265,"strand":1,"description":"trace amine associated receptor 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31925]"}, {"versioned_ensembl_gene_id":"ENSG00000139985.6","gene_symbol":"ADAM21","gene_name":"ADAM metallopeptidase domain 21 [Source:HGNC Symbol;Acc:HGNC:200]","synonyms":"ADAM31","biotype":"protein_coding","ncbi_id":"8747","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The expression of this gene expression is testis-specific. [provided by RefSeq, May 2011]","start":70452157,"end":70459899,"strand":1,"description":"ADAM metallopeptidase domain 21 [Source:HGNC Symbol;Acc:HGNC:200]"}, {"versioned_ensembl_gene_id":"ENSG00000242082.1","gene_symbol":"SLC5A4-AS1","gene_name":"SLC5A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53163]","synonyms":"RP1-90G24.10","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32205115,"end":32269666,"strand":1,"description":"SLC5A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53163]"}, {"versioned_ensembl_gene_id":"ENSG00000146383.7","gene_symbol":"TAAR6","gene_name":"trace amine associated receptor 6 [Source:HGNC Symbol;Acc:HGNC:20978]","synonyms":"TRAR4,TA4","biotype":"protein_coding","ncbi_id":"319100","summary":"This gene encodes a seven-transmembrane G-protein-coupled receptor that likely functions as a receptor for endogenous trace amines. Mutations in this gene may be associated with schizophrenia.[provided by RefSeq, Feb 2010]","start":132570322,"end":132571359,"strand":1,"description":"trace amine associated receptor 6 [Source:HGNC Symbol;Acc:HGNC:20978]"}, {"versioned_ensembl_gene_id":"ENSG00000186146.1","gene_symbol":"DEFB131A","gene_name":"defensin beta 131A [Source:HGNC Symbol;Acc:HGNC:18108]","synonyms":"DEFB131,DEFB-31","biotype":"protein_coding","ncbi_id":"644414","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 4p16. [provided by RefSeq, Nov 2014]","start":9444534,"end":9450514,"strand":1,"description":"defensin beta 131A [Source:HGNC Symbol;Acc:HGNC:18108]"}, {"versioned_ensembl_gene_id":"ENSG00000224395.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29456712,"end":29463860,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000253801.2","gene_symbol":"AC010376.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68087161,"end":68087494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100191.5","gene_symbol":"SLC5A4","gene_name":"solute carrier family 5 member 4 [Source:HGNC Symbol;Acc:HGNC:11039]","synonyms":"SGLT3,SAAT1,DJ90G24.4","biotype":"protein_coding","ncbi_id":"6527","summary":null,"start":32218476,"end":32255341,"strand":-1,"description":"solute carrier family 5 member 4 [Source:HGNC Symbol;Acc:HGNC:11039]"}, {"versioned_ensembl_gene_id":"ENSG00000236505.1","gene_symbol":"AL356379.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40563534,"end":40563659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259158.3","gene_symbol":"ADAM20P1","gene_name":"ADAM metallopeptidase domain 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20102]","synonyms":"C14orf55","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"317760","summary":null,"start":70468881,"end":70483756,"strand":-1,"description":"ADAM metallopeptidase domain 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20102]"}, {"versioned_ensembl_gene_id":"ENSG00000135569.4","gene_symbol":"TAAR5","gene_name":"trace amine associated receptor 5 [Source:HGNC Symbol;Acc:HGNC:30236]","synonyms":"PNR","biotype":"protein_coding","ncbi_id":"9038","summary":null,"start":132588673,"end":132589686,"strand":-1,"description":"trace amine associated receptor 5 [Source:HGNC Symbol;Acc:HGNC:30236]"}, {"versioned_ensembl_gene_id":"ENSG00000162892.15","gene_symbol":"IL24","gene_name":"interleukin 24 [Source:HGNC Symbol;Acc:HGNC:11346]","synonyms":"Mob-5,mda-7,IL10B,IL-24,FISP,C49A,ST16","biotype":"protein_coding","ncbi_id":"11009","summary":"This gene encodes a member of the IL10 family of cytokines. It was identified as a gene induced during terminal differentiation in melanoma cells. The protein encoded by this gene can induce apoptosis selectively in various cancer cells. Overexpression of this gene leads to elevated expression of several GADD family genes, which correlates with the induction of apoptosis. The phosphorylation of mitogen-activated protein kinase 14 (MAPK7/P38), and heat shock 27kDa protein 1 (HSPB2/HSP27) are found to be induced by this gene in melanoma cells, but not in normal immortal melanocytes. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":206897443,"end":206904139,"strand":1,"description":"interleukin 24 [Source:HGNC Symbol;Acc:HGNC:11346]"}, {"versioned_ensembl_gene_id":"ENSG00000248364.1","gene_symbol":"OR7E86P","gene_name":"olfactory receptor family 7 subfamily E member 86 pseudogene [Source:HGNC Symbol;Acc:HGNC:14694]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442104","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9459255,"end":9460244,"strand":1,"description":"olfactory receptor family 7 subfamily E member 86 pseudogene [Source:HGNC Symbol;Acc:HGNC:14694]"}, {"versioned_ensembl_gene_id":"ENSG00000154080.13","gene_symbol":"CHST9","gene_name":"carbohydrate sulfotransferase 9 [Source:HGNC Symbol;Acc:HGNC:19898]","synonyms":"GALNAC4ST-2,GALNAC-4-ST2","biotype":"protein_coding","ncbi_id":"83539","summary":"The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. Sulfate groups on carbohydrates confer highly specific functions to glycoproteins, glycolipids, and proteoglycans, and are critical for cell-cell interaction, signal transduction, and embryonic development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Aug 2011]","start":26906481,"end":27185317,"strand":-1,"description":"carbohydrate sulfotransferase 9 [Source:HGNC Symbol;Acc:HGNC:19898]"}, {"versioned_ensembl_gene_id":"ENSG00000213864.3","gene_symbol":"EEF1B2P2","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3209]","synonyms":"EEF1B3,EEF1B,EEF-1BETA5A,EEF-1,BETA-3","biotype":"processed_pseudogene","ncbi_id":"1934","summary":null,"start":68159218,"end":68159893,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3209]"}, {"versioned_ensembl_gene_id":"ENSG00000268995.1","gene_symbol":"VN1R82P","gene_name":"vomeronasal 1 receptor 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:37402]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312827","summary":null,"start":21188598,"end":21188953,"strand":1,"description":"vomeronasal 1 receptor 82 pseudogene [Source:HGNC Symbol;Acc:HGNC:37402]"}, {"versioned_ensembl_gene_id":"ENSG00000268598.1","gene_symbol":"VN1R80P","gene_name":"vomeronasal 1 receptor 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:37329]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312825","summary":null,"start":21063924,"end":21064261,"strand":1,"description":"vomeronasal 1 receptor 80 pseudogene [Source:HGNC Symbol;Acc:HGNC:37329]"}, {"versioned_ensembl_gene_id":"ENSG00000165572.7","gene_symbol":"KBTBD6","gene_name":"kelch repeat and BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:25340]","synonyms":"DKFZp547E1912","biotype":"protein_coding","ncbi_id":"89890","summary":null,"start":41127569,"end":41132746,"strand":-1,"description":"kelch repeat and BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:25340]"}, {"versioned_ensembl_gene_id":"ENSG00000271598.1","gene_symbol":"AC008739.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21025915,"end":21026041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224555.3","gene_symbol":"AC087441.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3989163,"end":3989463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253787.1","gene_symbol":"LINC02219","gene_name":"long intergenic non-protein coding RNA 2219 [Source:HGNC Symbol;Acc:HGNC:53086]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467655","summary":null,"start":68189876,"end":68198407,"strand":1,"description":"long intergenic non-protein coding RNA 2219 [Source:HGNC Symbol;Acc:HGNC:53086]"}, {"versioned_ensembl_gene_id":"ENSG00000213605.2","gene_symbol":"AC111200.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86885075,"end":86885731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268705.1","gene_symbol":"BNIP3P26","gene_name":"BCL2 interacting protein 3 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:49706]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421699","summary":null,"start":21521343,"end":21521896,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:49706]"}, {"versioned_ensembl_gene_id":"ENSG00000230593.3","gene_symbol":"AC090804.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3892398,"end":3892887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237449.1","gene_symbol":"TAAR4P","gene_name":"trace amine associated receptor 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:31924]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"503612","summary":null,"start":132594398,"end":132595436,"strand":-1,"description":"trace amine associated receptor 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:31924]"}, {"versioned_ensembl_gene_id":"ENSG00000196268.11","gene_symbol":"ZNF493","gene_name":"zinc finger protein 493 [Source:HGNC Symbol;Acc:HGNC:23708]","synonyms":"FLJ36504","biotype":"protein_coding","ncbi_id":"284443","summary":null,"start":21397119,"end":21427573,"strand":1,"description":"zinc finger protein 493 [Source:HGNC Symbol;Acc:HGNC:23708]"}, {"versioned_ensembl_gene_id":"ENSG00000233910.1","gene_symbol":"GTF2F2P2","gene_name":"general transcription factor IIF subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39092]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728633","summary":null,"start":40593633,"end":40594353,"strand":-1,"description":"general transcription factor IIF subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39092]"}, {"versioned_ensembl_gene_id":"ENSG00000179073.6","gene_symbol":"TAAR3P","gene_name":"trace amine associated receptor 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:4513]","synonyms":"TAAR3,GPR57","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"9288","summary":null,"start":132608225,"end":132609302,"strand":-1,"description":"trace amine associated receptor 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:4513]"}, {"versioned_ensembl_gene_id":"ENSG00000284689.1","gene_symbol":"AC097493.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9468974,"end":9469983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254521.6","gene_symbol":"SIGLEC12","gene_name":"sialic acid binding Ig like lectin 12 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15482]","synonyms":"Siglec-XII,Siglec-L1,Siglec-12,S2V,SLG,SIGLECL1","biotype":"protein_coding","ncbi_id":"89858","summary":"Sialic acid-binding immunoglobulin-like lectins (SIGLECs) are a family of cell surface proteins belonging to the immunoglobulin superfamily. They mediate protein-carbohydrate interactions by selectively binding to different sialic acid moieties present on glycolipids and glycoproteins. This gene encodes a member of the SIGLEC3-like subfamily of SIGLECs. Members of this subfamily are characterized by an extracellular V-set immunoglobulin-like domain followed by two C2-set immunoglobulin-like domains, and the cytoplasmic tyrosine-based motifs ITIM and SLAM-like. The encoded protein, upon tyrosine phosphorylation, has been shown to recruit the Src homology 2 domain-containing protein-tyrosine phosphatases SHP1 and SHP2. It has been suggested that the protein is involved in the negative regulation of macrophage signaling by functioning as an inhibitory receptor. This gene is located in a cluster with other SIGLEC3-like genes on 19q13.4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":51491357,"end":51501789,"strand":-1,"description":"sialic acid binding Ig like lectin 12 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15482]"}, {"versioned_ensembl_gene_id":"ENSG00000206485.10","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30665910,"end":30677416,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000258430.1","gene_symbol":"AL583722.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104769349,"end":104770271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224378.9","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31480101,"end":31493317,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000136872.17","gene_symbol":"ALDOB","gene_name":"aldolase, fructose-bisphosphate B [Source:HGNC Symbol;Acc:HGNC:417]","synonyms":null,"biotype":"protein_coding","ncbi_id":"229","summary":"Fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high degree of homology between aldolase A and C. Defects in ALDOB cause hereditary fructose intolerance. [provided by RefSeq, Dec 2008]","start":101420578,"end":101435823,"strand":-1,"description":"aldolase, fructose-bisphosphate B [Source:HGNC Symbol;Acc:HGNC:417]"}, {"versioned_ensembl_gene_id":"ENSG00000275805.1","gene_symbol":"AC090206.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26565723,"end":26575626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213049.3","gene_symbol":"HNRNPA1P34","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:48763]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996501","summary":null,"start":9027532,"end":9029089,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:48763]"}, {"versioned_ensembl_gene_id":"ENSG00000171885.13","gene_symbol":"AQP4","gene_name":"aquaporin 4 [Source:HGNC Symbol;Acc:HGNC:637]","synonyms":"MIWC","biotype":"protein_coding","ncbi_id":"361","summary":"This gene encodes a member of the aquaporin family of intrinsic membrane proteins that function as water-selective channels in the plasma membranes of many cells. This protein is the predominant aquaporin found in brain and has an important role in brain water homeostasis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. Additional isoforms, resulting from the use of alternative in-frame translation initiation codons, have also been described. Recent studies provided evidence for translational readthrough in this gene, and expression of C-terminally extended isoforms via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Jun 2018]","start":26852038,"end":26865818,"strand":-1,"description":"aquaporin 4 [Source:HGNC Symbol;Acc:HGNC:637]"}, {"versioned_ensembl_gene_id":"ENSG00000135972.8","gene_symbol":"MRPS9","gene_name":"mitochondrial ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:14501]","synonyms":"MRP-S9,S9mt,RPMS9","biotype":"protein_coding","ncbi_id":"64965","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. [provided by RefSeq, Jul 2008]","start":105037983,"end":105099960,"strand":1,"description":"mitochondrial ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:14501]"}, {"versioned_ensembl_gene_id":"ENSG00000266985.1","gene_symbol":"AC010485.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33555568,"end":33557470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213337.8","gene_symbol":"ANKRD39","gene_name":"ankyrin repeat domain 39 [Source:HGNC Symbol;Acc:HGNC:28640]","synonyms":"MGC41816","biotype":"protein_coding","ncbi_id":"51239","summary":null,"start":96836611,"end":96858095,"strand":-1,"description":"ankyrin repeat domain 39 [Source:HGNC Symbol;Acc:HGNC:28640]"}, {"versioned_ensembl_gene_id":"ENSG00000146399.1","gene_symbol":"TAAR1","gene_name":"trace amine associated receptor 1 [Source:HGNC Symbol;Acc:HGNC:17734]","synonyms":"TRAR1,TAR1,TA1","biotype":"protein_coding","ncbi_id":"134864","summary":"The protein encoded by this gene is a G-protein coupled receptor activated by trace amines. The encoded protein responds little or not at all to dopamine, serotonin, epinephrine, or histamine, but responds well to beta-phenylethylamine, p-tyramine, octopamine, and tryptamine. While primarily functioning in neurologic systems, there is evidence that this gene is involved in blood cell and immunologic functions as well. This gene is thought to be intronless. [provided by RefSeq, Nov 2015]","start":132644984,"end":132646003,"strand":-1,"description":"trace amine associated receptor 1 [Source:HGNC Symbol;Acc:HGNC:17734]"}, {"versioned_ensembl_gene_id":"ENSG00000223716.2","gene_symbol":"AL135785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38360427,"end":38376430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232429.3","gene_symbol":"RPL21P131","gene_name":"ribosomal protein L21 pseudogene 131 [Source:HGNC Symbol;Acc:HGNC:36428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388532","summary":null,"start":33589206,"end":33589688,"strand":-1,"description":"ribosomal protein L21 pseudogene 131 [Source:HGNC Symbol;Acc:HGNC:36428]"}, {"versioned_ensembl_gene_id":"ENSG00000225133.1","gene_symbol":"MORF4L1P4","gene_name":"mortality factor 4 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39257]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420030","summary":null,"start":41199832,"end":41200807,"strand":-1,"description":"mortality factor 4 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39257]"}, {"versioned_ensembl_gene_id":"ENSG00000218194.1","gene_symbol":"HLFP1","gene_name":"hepatic leukemia factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873813","summary":null,"start":132674885,"end":132675383,"strand":1,"description":"hepatic leukemia factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41922]"}, {"versioned_ensembl_gene_id":"ENSG00000278390.4","gene_symbol":"AL354696.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41132939,"end":41236686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268357.1","gene_symbol":"VN1R81P","gene_name":"vomeronasal 1 receptor 81 pseudogene [Source:HGNC Symbol;Acc:HGNC:37401]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312826","summary":null,"start":21123817,"end":21124188,"strand":1,"description":"vomeronasal 1 receptor 81 pseudogene [Source:HGNC Symbol;Acc:HGNC:37401]"}, {"versioned_ensembl_gene_id":"ENSG00000269012.2","gene_symbol":"KRT18P40","gene_name":"keratin 18 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:33409]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390904","summary":null,"start":20961057,"end":20965140,"strand":1,"description":"keratin 18 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:33409]"}, {"versioned_ensembl_gene_id":"ENSG00000184205.14","gene_symbol":"TSPYL2","gene_name":"TSPY like 2 [Source:HGNC Symbol;Acc:HGNC:24358]","synonyms":"TSPX,SE20-4,HRIHFB2216,DENTT,CTCL,CINAP,CDA1","biotype":"protein_coding","ncbi_id":"64061","summary":"This gene encodes a member of the testis-specific protein Y-encoded, TSPY-like/SET/nucleosome assembly protein-1 superfamily. The encoded protein is localized to the nucleolus where it functions in chromatin remodeling and as an inhibitor of cell-cycle progression. This protein may play a role in the suppression of tumor growth. [provided by RefSeq, Sep 2009]","start":53082367,"end":53088540,"strand":1,"description":"TSPY like 2 [Source:HGNC Symbol;Acc:HGNC:24358]"}, {"versioned_ensembl_gene_id":"ENSG00000137124.7","gene_symbol":"ALDH1B1","gene_name":"aldehyde dehydrogenase 1 family member B1 [Source:HGNC Symbol;Acc:HGNC:407]","synonyms":"ALDHX,ALDH5","biotype":"protein_coding","ncbi_id":"219","summary":"This protein belongs to the aldehyde dehydrogenases family of proteins. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. This gene does not contain introns in the coding sequence. The variation of this locus may affect the development of alcohol-related problems. [provided by RefSeq, Jul 2008]","start":38392664,"end":38398661,"strand":1,"description":"aldehyde dehydrogenase 1 family member B1 [Source:HGNC Symbol;Acc:HGNC:407]"}, {"versioned_ensembl_gene_id":"ENSG00000277662.1","gene_symbol":"AL354696.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41229180,"end":41229676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182324.6","gene_symbol":"KCNJ14","gene_name":"potassium voltage-gated channel subfamily J member 14 [Source:HGNC Symbol;Acc:HGNC:6260]","synonyms":"Kir2.4,IRK4","biotype":"protein_coding","ncbi_id":"3770","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel, and probably has a role in controlling the excitability of motor neurons. [provided by RefSeq, Feb 2013]","start":48455509,"end":48466980,"strand":1,"description":"potassium voltage-gated channel subfamily J member 14 [Source:HGNC Symbol;Acc:HGNC:6260]"}, {"versioned_ensembl_gene_id":"ENSG00000105750.14","gene_symbol":"ZNF85","gene_name":"zinc finger protein 85 [Source:HGNC Symbol;Acc:HGNC:13160]","synonyms":"HTF1,HPF4","biotype":"protein_coding","ncbi_id":"7639","summary":null,"start":20923222,"end":20950697,"strand":1,"description":"zinc finger protein 85 [Source:HGNC Symbol;Acc:HGNC:13160]"}, {"versioned_ensembl_gene_id":"ENSG00000120662.15","gene_symbol":"MTRF1","gene_name":"mitochondrial translation release factor 1 [Source:HGNC Symbol;Acc:HGNC:7469]","synonyms":"RF1,MTTRF1,MGC47721","biotype":"protein_coding","ncbi_id":"9617","summary":"The protein encoded by this gene was determined by in silico methods to be a mitochondrial protein with similarity to the peptide chain release factors (RFs) discovered in bacteria and yeast. The peptide chain release factors direct the termination of translation in response to the peptide chain termination codons. Initially thought to have a role in the termination of mitochondria protein synthesis, a recent publication found no mitochondrial translation release functionality. Multiple alternatively spliced transcript variants have been suggested by mRNA and EST data; however, their full-length natures are not clear. [provided by RefSeq, Jul 2008]","start":41216369,"end":41263577,"strand":-1,"description":"mitochondrial translation release factor 1 [Source:HGNC Symbol;Acc:HGNC:7469]"}, {"versioned_ensembl_gene_id":"ENSG00000267470.5","gene_symbol":"ZNF571-AS1","gene_name":"ZNF571 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44324]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507433","summary":null,"start":37548914,"end":37587348,"strand":1,"description":"ZNF571 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44324]"}, {"versioned_ensembl_gene_id":"ENSG00000248740.5","gene_symbol":"LINC02428","gene_name":"long intergenic non-protein coding RNA 2428 [Source:HGNC Symbol;Acc:HGNC:53359]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929448","summary":null,"start":103256159,"end":103453658,"strand":1,"description":"long intergenic non-protein coding RNA 2428 [Source:HGNC Symbol;Acc:HGNC:53359]"}, {"versioned_ensembl_gene_id":"ENSG00000231851.5","gene_symbol":"UTAT33","gene_name":"uncharacterized LOC101927492 [Source:NCBI gene;Acc:101927492]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927492","summary":null,"start":105097052,"end":105102944,"strand":-1,"description":"uncharacterized LOC101927492 [Source:NCBI gene;Acc:101927492]"}, {"versioned_ensembl_gene_id":"ENSG00000145882.10","gene_symbol":"PCYOX1L","gene_name":"prenylcysteine oxidase 1 like [Source:HGNC Symbol;Acc:HGNC:28477]","synonyms":"MGC3265","biotype":"protein_coding","ncbi_id":"78991","summary":null,"start":149358007,"end":149369653,"strand":1,"description":"prenylcysteine oxidase 1 like [Source:HGNC Symbol;Acc:HGNC:28477]"}, {"versioned_ensembl_gene_id":"ENSG00000105447.12","gene_symbol":"GRWD1","gene_name":"glutamate rich WD repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:21270]","synonyms":"WDR28,RRB1,GRWD","biotype":"protein_coding","ncbi_id":"83743","summary":"This gene encodes a glutamate-rich protein that contains five WD-repeat motifs. The encoded protein may play a critical role in ribosome biogenesis and may also play a role in histone methylation through interactions with CUL4-DDB1 ubiquitin E3 ligase. [provided by RefSeq, Feb 2012]","start":48445773,"end":48457022,"strand":1,"description":"glutamate rich WD repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:21270]"}, {"versioned_ensembl_gene_id":"ENSG00000234801.3","gene_symbol":"MORF4","gene_name":"mortality factor 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15773]","synonyms":"SEN1,SEN","biotype":"processed_pseudogene","ncbi_id":"10934","summary":"Cellular senescence, the terminal nondividing state that normal cells enter following completion of their proliferative potential, is the dominant phenotype in hybrids of normal and immortal cells. Fusions of immortal human cell lines with each other have led to their assignment to 1 of several complementation groups. MORF4 is a gene on chromosome 4 that induces a senescent-like phenotype in cell lines assigned to complementation group B.[supplied by OMIM, Apr 2004]","start":173615936,"end":173616906,"strand":-1,"description":"mortality factor 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15773]"}, {"versioned_ensembl_gene_id":"ENSG00000253107.1","gene_symbol":"AC090819.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110555408,"end":110556518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112299.7","gene_symbol":"VNN1","gene_name":"vanin 1 [Source:HGNC Symbol;Acc:HGNC:12705]","synonyms":"Tiff66","biotype":"protein_coding","ncbi_id":"8876","summary":"This gene encodes a member of the vanin family of proteins, which share extensive sequence similarity with each other, and also with biotinidase. The family includes secreted and membrane-associated proteins, a few of which have been reported to participate in hematopoietic cell trafficking. No biotinidase activity has been demonstrated for any of the vanin proteins, however, they possess pantetheinase activity, which may play a role in oxidative-stress response. This protein, like its mouse homolog, is likely a GPI-anchored cell surface molecule. The mouse protein is expressed by the perivascular thymic stromal cells and regulates migration of T-cell progenitors to the thymus. This gene lies in close proximity to, and in the same transcriptional orientation as, two other vanin genes on chromosome 6q23-q24. [provided by RefSeq, Feb 2009]","start":132681590,"end":132714049,"strand":-1,"description":"vanin 1 [Source:HGNC Symbol;Acc:HGNC:12705]"}, {"versioned_ensembl_gene_id":"ENSG00000213370.3","gene_symbol":"RANP6","gene_name":"RAN, member RAS oncogene family pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39861]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128266","summary":null,"start":173633728,"end":173634371,"strand":-1,"description":"RAN, member RAS oncogene family pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39861]"}, {"versioned_ensembl_gene_id":"ENSG00000278114.4","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195720882,"end":195741123,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000249064.1","gene_symbol":"KRT18P25","gene_name":"keratin 18 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:33394]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391647","summary":null,"start":40020240,"end":40021517,"strand":1,"description":"keratin 18 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:33394]"}, {"versioned_ensembl_gene_id":"ENSG00000224509.2","gene_symbol":"AC010884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104936241,"end":105038496,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253122.1","gene_symbol":"AC025366.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110609241,"end":110632394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253573.1","gene_symbol":"AC024382.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126766876,"end":126790637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270982.1","gene_symbol":"AL353621.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101449801,"end":101449933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253717.1","gene_symbol":"AP005357.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110766863,"end":110772759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250920.1","gene_symbol":"AC105460.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103550927,"end":103559127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226365.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464128,"end":29469338,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000250222.1","gene_symbol":"AC008443.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181191924,"end":181194429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251577.5","gene_symbol":"AC105460.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103548745,"end":103624534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271339.1","gene_symbol":"AL683813.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136788286,"end":136788787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272274.1","gene_symbol":"LINC00551","gene_name":"long intergenic non-protein coding RNA 551 [Source:HGNC Symbol;Acc:HGNC:43691]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283483","summary":null,"start":106617810,"end":106631359,"strand":1,"description":"long intergenic non-protein coding RNA 551 [Source:HGNC Symbol;Acc:HGNC:43691]"}, {"versioned_ensembl_gene_id":"ENSG00000250900.6","gene_symbol":"AC008443.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181195496,"end":181203103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255132.1","gene_symbol":"AC090138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41394595,"end":41426504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253438.2","gene_symbol":"PCAT1","gene_name":"prostate cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43022]","synonyms":"PCAT-1,PCA1","biotype":"lincRNA","ncbi_id":"100750225","summary":"This gene produces a long non-coding RNA that promotes cell proliferation and is upregulated in prostate, colorectal, and other cancers. This RNA negatively regulates the BRCA2 tumor suppressor protein and positively regulates Myc oncoprotein. It contains binding sites for microRNAs, and may act as a sponge for microRNAs that regulate cell growth pathways. [provided by RefSeq, Dec 2017]","start":126847055,"end":127021014,"strand":1,"description":"prostate cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43022]"}, {"versioned_ensembl_gene_id":"ENSG00000233055.1","gene_symbol":"AL353621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101501643,"end":101501885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148948.7","gene_symbol":"LRRC4C","gene_name":"leucine rich repeat containing 4C [Source:HGNC Symbol;Acc:HGNC:29317]","synonyms":"NGL-1,KIAA1580","biotype":"protein_coding","ncbi_id":"57689","summary":"NGL1 is a specific binding partner for netrin G1 (NTNG1; MIM 608818), which is a member of the netrin family of axon guidance molecules (Lin et al., 2003 [PubMed 14595443]).[supplied by OMIM, Mar 2008]","start":40114203,"end":41459773,"strand":-1,"description":"leucine rich repeat containing 4C [Source:HGNC Symbol;Acc:HGNC:29317]"}, {"versioned_ensembl_gene_id":"ENSG00000242282.6","gene_symbol":"AC108488.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3531813,"end":3536873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165152.8","gene_symbol":"TMEM246","gene_name":"transmembrane protein 246 [Source:HGNC Symbol;Acc:HGNC:28180]","synonyms":"C9orf125,MGC12992","biotype":"protein_coding","ncbi_id":"84302","summary":null,"start":101473171,"end":101533537,"strand":-1,"description":"transmembrane protein 246 [Source:HGNC Symbol;Acc:HGNC:28180]"}, {"versioned_ensembl_gene_id":"ENSG00000230957.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29474557,"end":29475603,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000218991.1","gene_symbol":"CCNG1P1","gene_name":"cyclin G1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39177]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130820","summary":null,"start":132698783,"end":132699667,"strand":1,"description":"cyclin G1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39177]"}, {"versioned_ensembl_gene_id":"ENSG00000227590.2","gene_symbol":"ATP5G1P5","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39508]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390424","summary":null,"start":106663437,"end":106663847,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39508]"}, {"versioned_ensembl_gene_id":"ENSG00000169836.4","gene_symbol":"TACR3","gene_name":"tachykinin receptor 3 [Source:HGNC Symbol;Acc:HGNC:11528]","synonyms":"NK3R","biotype":"protein_coding","ncbi_id":"6870","summary":"This gene belongs to a family of genes that function as receptors for tachykinins. Receptor affinities are specified by variations in the 5'-end of the sequence. The receptors belonging to this family are characterized by interactions with G proteins and 7 hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin neurokinin 3, also referred to as neurokinin B. [provided by RefSeq, Jul 2008]","start":103586031,"end":103719816,"strand":-1,"description":"tachykinin receptor 3 [Source:HGNC Symbol;Acc:HGNC:11528]"}, {"versioned_ensembl_gene_id":"ENSG00000278126.1","gene_symbol":"AC139768.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51201684,"end":51202581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248514.1","gene_symbol":"AC008443.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181205361,"end":181206120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235289.1","gene_symbol":"BRD7P6","gene_name":"bromodomain containing 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37632]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128042","summary":null,"start":70353010,"end":70355915,"strand":1,"description":"bromodomain containing 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37632]"}, {"versioned_ensembl_gene_id":"ENSG00000184271.16","gene_symbol":"POU6F1","gene_name":"POU class 6 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9224]","synonyms":"BRN5,TCFB1,MPOU","biotype":"protein_coding","ncbi_id":"5463","summary":null,"start":51186936,"end":51217708,"strand":-1,"description":"POU class 6 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9224]"}, {"versioned_ensembl_gene_id":"ENSG00000256888.5","gene_symbol":"LINC02366","gene_name":"long intergenic non-protein coding RNA 2366 [Source:HGNC Symbol;Acc:HGNC:53289]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928162","summary":null,"start":10750234,"end":10777444,"strand":1,"description":"long intergenic non-protein coding RNA 2366 [Source:HGNC Symbol;Acc:HGNC:53289]"}, {"versioned_ensembl_gene_id":"ENSG00000244573.3","gene_symbol":"RPL30P11","gene_name":"ribosomal protein L30 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36260]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271303","summary":null,"start":14356842,"end":14365503,"strand":-1,"description":"ribosomal protein L30 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36260]"}, {"versioned_ensembl_gene_id":"ENSG00000232367.5","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32767527,"end":32776296,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000279019.1","gene_symbol":"AC009090.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57140896,"end":57144586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240661.3","gene_symbol":"AC063952.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":120349449,"end":120423826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231297.3","gene_symbol":"AL627443.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166099665,"end":166113273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065548.17","gene_symbol":"ZC3H15","gene_name":"zinc finger CCCH-type containing 15 [Source:HGNC Symbol;Acc:HGNC:29528]","synonyms":"LEREPO4","biotype":"protein_coding","ncbi_id":"55854","summary":null,"start":186486156,"end":186509363,"strand":1,"description":"zinc finger CCCH-type containing 15 [Source:HGNC Symbol;Acc:HGNC:29528]"}, {"versioned_ensembl_gene_id":"ENSG00000101220.17","gene_symbol":"C20orf27","gene_name":"chromosome 20 open reading frame 27 [Source:HGNC Symbol;Acc:HGNC:15873]","synonyms":"FLJ20550","biotype":"protein_coding","ncbi_id":"54976","summary":null,"start":3753508,"end":3768387,"strand":-1,"description":"chromosome 20 open reading frame 27 [Source:HGNC Symbol;Acc:HGNC:15873]"}, {"versioned_ensembl_gene_id":"ENSG00000165923.15","gene_symbol":"AGBL2","gene_name":"ATP/GTP binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:26296]","synonyms":"FLJ23598,CCP2","biotype":"protein_coding","ncbi_id":"79841","summary":null,"start":47659591,"end":47715389,"strand":-1,"description":"ATP/GTP binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:26296]"}, {"versioned_ensembl_gene_id":"ENSG00000249516.1","gene_symbol":"PRELID3BP6","gene_name":"PRELI domain containing 3B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132940","summary":null,"start":42917414,"end":42917984,"strand":1,"description":"PRELI domain containing 3B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49068]"}, {"versioned_ensembl_gene_id":"ENSG00000223693.3","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"SUCLA2P,Em:AB014080.4","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30458389,"end":30459758,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000250358.5","gene_symbol":"LINC02200","gene_name":"long intergenic non-protein coding RNA 2200 [Source:HGNC Symbol;Acc:HGNC:53066]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467214","summary":null,"start":112628436,"end":112632100,"strand":1,"description":"long intergenic non-protein coding RNA 2200 [Source:HGNC Symbol;Acc:HGNC:53066]"}, {"versioned_ensembl_gene_id":"ENSG00000230355.1","gene_symbol":"AC009474.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66881087,"end":66881222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277268.1","gene_symbol":"AC243773.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36861674,"end":36936661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235368.1","gene_symbol":"SAPCD2P2","gene_name":"suppressor APC domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51278]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442317","summary":null,"start":57424503,"end":57425676,"strand":1,"description":"suppressor APC domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51278]"}, {"versioned_ensembl_gene_id":"ENSG00000134597.15","gene_symbol":"RBMX2","gene_name":"RNA binding motif protein, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:24282]","synonyms":"CGI-79,Snu17","biotype":"protein_coding","ncbi_id":"51634","summary":null,"start":130401969,"end":130413343,"strand":1,"description":"RNA binding motif protein, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:24282]"}, {"versioned_ensembl_gene_id":"ENSG00000231034.1","gene_symbol":"AL118520.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34688688,"end":34688978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182195.7","gene_symbol":"LDOC1","gene_name":"LDOC1, regulator of NFKB signaling [Source:HGNC Symbol;Acc:HGNC:6548]","synonyms":"BCUR1,SIRH7,RTL7,Mart7,Mar7","biotype":"protein_coding","ncbi_id":"23641","summary":"The protein encoded by this gene contains a leucine zipper-like motif and a proline-rich region that shares marked similarity with an SH3-binding domain. The protein localizes to the nucleus and is down-regulated in some cancer cell lines. It is thought to regulate the transcriptional response mediated by the nuclear factor kappa B (NF-kappaB). The gene has been proposed as a tumor suppressor gene whose protein product may have an important role in the development and/or progression of some cancers. [provided by RefSeq, Jul 2008]","start":141175745,"end":141177125,"strand":-1,"description":"LDOC1, regulator of NFKB signaling [Source:HGNC Symbol;Acc:HGNC:6548]"}, {"versioned_ensembl_gene_id":"ENSG00000266416.1","gene_symbol":"AC130289.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27708111,"end":27708138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271652.1","gene_symbol":"AL356052.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54116476,"end":54116851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251014.1","gene_symbol":"AC137549.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112546973,"end":112547505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267223.1","gene_symbol":"AC005597.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30219666,"end":30228715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227692.1","gene_symbol":"MED28P3","gene_name":"mediator complex subunit 28 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45080]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131051","summary":null,"start":186364598,"end":186365128,"strand":1,"description":"mediator complex subunit 28 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45080]"}, {"versioned_ensembl_gene_id":"ENSG00000265041.1","gene_symbol":"AC015688.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27666749,"end":27672803,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235223.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"Em:AB014080.3,TMPOL1","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30456041,"end":30457570,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000259915.2","gene_symbol":"AC017071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186354570,"end":186356773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266910.1","gene_symbol":"AC008507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30037423,"end":30038156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267692.1","gene_symbol":"AC008507.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30037285,"end":30037411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258313.1","gene_symbol":"AC084879.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95387890,"end":95388558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223918.1","gene_symbol":"AL513328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110727456,"end":110727679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240957.1","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"G6f,NG32,C6orf21,LY6G6D","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31783165,"end":31786875,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000260148.1","gene_symbol":"AC009090.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57091213,"end":57092303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115239.21","gene_symbol":"ASB3","gene_name":"ankyrin repeat and SOCS box containing 3 [Source:HGNC Symbol;Acc:HGNC:16013]","synonyms":"ASB-3","biotype":"protein_coding","ncbi_id":"51130","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jan 2011]","start":53532672,"end":53787610,"strand":-1,"description":"ankyrin repeat and SOCS box containing 3 [Source:HGNC Symbol;Acc:HGNC:16013]"}, {"versioned_ensembl_gene_id":"ENSG00000275194.1","gene_symbol":"AC004467.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11221348,"end":11225731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120669.15","gene_symbol":"SOHLH2","gene_name":"spermatogenesis and oogenesis specific basic helix-loop-helix 2 [Source:HGNC Symbol;Acc:HGNC:26026]","synonyms":"TEB1,SPATA28,FLJ20449,bHLHe81","biotype":"protein_coding","ncbi_id":"54937","summary":"This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis-specific transcription factor, SOHLH1, can form heterodimers, in addition to homodimers. There is a read-through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":36168208,"end":36214615,"strand":-1,"description":"spermatogenesis and oogenesis specific basic helix-loop-helix 2 [Source:HGNC Symbol;Acc:HGNC:26026]"}, {"versioned_ensembl_gene_id":"ENSG00000229082.1","gene_symbol":"OR5AW1P","gene_name":"olfactory receptor family 5 subfamily AW member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"81076","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131341447,"end":131342452,"strand":-1,"description":"olfactory receptor family 5 subfamily AW member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15406]"}, {"versioned_ensembl_gene_id":"ENSG00000273062.1","gene_symbol":"AL449106.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178724306,"end":178726285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000030304.13","gene_symbol":"MUSK","gene_name":"muscle associated receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4593","summary":"This gene encodes a muscle-specific tyrosine kinase receptor. The encoded protein may play a role in clustering of the acetylcholine receptor in the postsynaptic neuromuscular junction. Mutations in this gene have been associated with congenital myasthenic syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Oct 2009]","start":110668771,"end":110801620,"strand":1,"description":"muscle associated receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7525]"}, {"versioned_ensembl_gene_id":"ENSG00000282658.1","gene_symbol":"AC012572.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78505165,"end":78506410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000062524.15","gene_symbol":"LTK","gene_name":"leukocyte receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6721]","synonyms":"TYK1","biotype":"protein_coding","ncbi_id":"4058","summary":"The protein encoded by this gene is a member of the ros/insulin receptor family of tyrosine kinases. Tyrosine-specific phosphorylation of proteins is a key to the control of diverse pathways leading to cell growth and differentiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":41503638,"end":41513887,"strand":-1,"description":"leukocyte receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6721]"}, {"versioned_ensembl_gene_id":"ENSG00000257037.1","gene_symbol":"RARSP1","gene_name":"arginyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419829","summary":null,"start":27496937,"end":27498589,"strand":1,"description":"arginyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49893]"}, {"versioned_ensembl_gene_id":"ENSG00000284671.1","gene_symbol":"AC009093.9","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29075022,"end":29104162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260953.1","gene_symbol":"AC009093.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29262273,"end":29264479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259807.1","gene_symbol":"AC009093.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29217170,"end":29220031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278558.4","gene_symbol":"TMEM191B","gene_name":"transmembrane protein 191B [Source:HGNC Symbol;Acc:HGNC:33600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728229","summary":null,"start":18527802,"end":18530573,"strand":1,"description":"transmembrane protein 191B [Source:HGNC Symbol;Acc:HGNC:33600]"}, {"versioned_ensembl_gene_id":"ENSG00000232732.9","gene_symbol":"AC097717.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":199867396,"end":199911159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006831.9","gene_symbol":"ADIPOR2","gene_name":"adiponectin receptor 2 [Source:HGNC Symbol;Acc:HGNC:24041]","synonyms":"ACDCR2,PAQR2","biotype":"protein_coding","ncbi_id":"79602","summary":"The adiponectin receptors, ADIPOR1 (MIM 607945) and ADIPOR2, serve as receptors for globular and full-length adiponectin (MIM 605441) and mediate increased AMPK (see MIM 602739) and PPAR-alpha (PPARA; MIM 170998) ligand activities, as well as fatty acid oxidation and glucose uptake by adiponectin (Yamauchi et al., 2003 [PubMed 12802337]).[supplied by OMIM, Mar 2008]","start":1688574,"end":1788678,"strand":1,"description":"adiponectin receptor 2 [Source:HGNC Symbol;Acc:HGNC:24041]"}, {"versioned_ensembl_gene_id":"ENSG00000278283.1","gene_symbol":"AL020991.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55044749,"end":55045121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234222.6","gene_symbol":"LIX1L-AS1","gene_name":"LIX1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41210]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105371260","summary":null,"start":145926590,"end":145959179,"strand":1,"description":"LIX1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41210]"}, {"versioned_ensembl_gene_id":"ENSG00000106624.10","gene_symbol":"AEBP1","gene_name":"AE binding protein 1 [Source:HGNC Symbol;Acc:HGNC:303]","synonyms":"ACLP","biotype":"protein_coding","ncbi_id":"165","summary":"This gene encodes a member of carboxypeptidase A protein family. The encoded protein may function as a transcriptional repressor and play a role in adipogenesis and smooth muscle cell differentiation. Studies in mice suggest that this gene functions in wound healing and abdominal wall development. Overexpression of this gene is associated with glioblastoma. [provided by RefSeq, May 2013]","start":44104361,"end":44114562,"strand":1,"description":"AE binding protein 1 [Source:HGNC Symbol;Acc:HGNC:303]"}, {"versioned_ensembl_gene_id":"ENSG00000198678.5","gene_symbol":"AC089987.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48559882,"end":48562956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278619.4","gene_symbol":"MRM1","gene_name":"mitochondrial rRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26202]","synonyms":"FLJ22578","biotype":"protein_coding","ncbi_id":"79922","summary":null,"start":36601572,"end":36608971,"strand":1,"description":"mitochondrial rRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26202]"}, {"versioned_ensembl_gene_id":"ENSG00000110435.11","gene_symbol":"PDHX","gene_name":"pyruvate dehydrogenase complex component X [Source:HGNC Symbol;Acc:HGNC:21350]","synonyms":"proX,PDX1,OPDX,E3BP,DLDBP","biotype":"protein_coding","ncbi_id":"8050","summary":"The pyruvate dehydrogenase (PDH) complex is located in the mitochondrial matrix and catalyzes the conversion of pyruvate to acetyl coenzyme A. The PDH complex thereby links glycolysis to Krebs cycle. The PDH complex contains three catalytic subunits, E1, E2, and E3, two regulatory subunits, E1 kinase and E1 phosphatase, and a non-catalytic subunit, E3 binding protein (E3BP). This gene encodes the E3 binding protein subunit; also known as component X of the pyruvate dehydrogenase complex. This protein tethers E3 dimers to the E2 core of the PDH complex. Defects in this gene are a cause of pyruvate dehydrogenase deficiency which results in neurological dysfunction and lactic acidosis in infancy and early childhood. This protein is also a minor antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC eventually leads to cirrhosis and liver failure. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]","start":34915829,"end":35020591,"strand":1,"description":"pyruvate dehydrogenase complex component X [Source:HGNC Symbol;Acc:HGNC:21350]"}, {"versioned_ensembl_gene_id":"ENSG00000135502.17","gene_symbol":"SLC26A10","gene_name":"solute carrier family 26 member 10 [Source:HGNC Symbol;Acc:HGNC:14470]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65012","summary":null,"start":57619527,"end":57626151,"strand":1,"description":"solute carrier family 26 member 10 [Source:HGNC Symbol;Acc:HGNC:14470]"}, {"versioned_ensembl_gene_id":"ENSG00000206461.4","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31103629,"end":31104965,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000284558.1","gene_symbol":"AC099654.14","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57191997,"end":57192337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228851.1","gene_symbol":"MTCO3P4","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52079]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075216","summary":null,"start":57191141,"end":57191927,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52079]"}, {"versioned_ensembl_gene_id":"ENSG00000229199.5","gene_symbol":"AL805909.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31000494,"end":31025446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140451.12","gene_symbol":"PIF1","gene_name":"PIF1 5'-to-3' DNA helicase [Source:HGNC Symbol;Acc:HGNC:26220]","synonyms":"FLJ22692,C15orf20","biotype":"protein_coding","ncbi_id":"80119","summary":"This gene encodes a DNA-dependent adenosine triphosphate (ATP)-metabolizing enzyme that functions as a 5' to 3' DNA helicase. The encoded protein can resolve G-quadruplex structures and RNA-DNA hybrids at the ends of chromosomes. It also prevents telomere elongation by inhibiting the actions of telomerase. Alternative splicing and the use of alternative start codons results in multiple isoforms that are differentially localized to either the mitochondria or the nucleus. [provided by RefSeq, Nov 2013]","start":64815632,"end":64825668,"strand":-1,"description":"PIF1 5'-to-3' DNA helicase [Source:HGNC Symbol;Acc:HGNC:26220]"}, {"versioned_ensembl_gene_id":"ENSG00000284291.1","gene_symbol":"AC099654.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57189578,"end":57190226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150667.6","gene_symbol":"FSIP1","gene_name":"fibrous sheath interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21674]","synonyms":"FLJ35989","biotype":"protein_coding","ncbi_id":"161835","summary":null,"start":39600031,"end":39782830,"strand":-1,"description":"fibrous sheath interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21674]"}, {"versioned_ensembl_gene_id":"ENSG00000277033.2","gene_symbol":"B3GNTL1","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:21727]","synonyms":"B3GNT8","biotype":"protein_coding","ncbi_id":"146712","summary":null,"start":82942371,"end":83050530,"strand":-1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:21727]"}, {"versioned_ensembl_gene_id":"ENSG00000226102.3","gene_symbol":"SEPT7P3","gene_name":"septin 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38038]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646913","summary":null,"start":35946294,"end":35972587,"strand":1,"description":"septin 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38038]"}, {"versioned_ensembl_gene_id":"ENSG00000178358.4","gene_symbol":"OR2D3","gene_name":"olfactory receptor family 2 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:15146]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120775","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6920974,"end":6922043,"strand":1,"description":"olfactory receptor family 2 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:15146]"}, {"versioned_ensembl_gene_id":"ENSG00000142669.14","gene_symbol":"SH3BGRL3","gene_name":"SH3 domain binding glutamate rich protein like 3 [Source:HGNC Symbol;Acc:HGNC:15568]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83442","summary":null,"start":26279176,"end":26281522,"strand":1,"description":"SH3 domain binding glutamate rich protein like 3 [Source:HGNC Symbol;Acc:HGNC:15568]"}, {"versioned_ensembl_gene_id":"ENSG00000281487.1","gene_symbol":"AC139677.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46706769,"end":46708058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169442.8","gene_symbol":"CD52","gene_name":"CD52 molecule [Source:HGNC Symbol;Acc:HGNC:1804]","synonyms":"HE5,EDDM5,CDW52","biotype":"protein_coding","ncbi_id":"1043","summary":null,"start":26317957,"end":26320523,"strand":1,"description":"CD52 molecule [Source:HGNC Symbol;Acc:HGNC:1804]"}, {"versioned_ensembl_gene_id":"ENSG00000225834.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32338729,"end":32341897,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000271595.1","gene_symbol":"ELOCP35","gene_name":"elongin C pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:49176]","synonyms":"TCEB1P35","biotype":"processed_pseudogene","ncbi_id":"106480250","summary":null,"start":17464879,"end":17465214,"strand":-1,"description":"elongin C pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:49176]"}, {"versioned_ensembl_gene_id":"ENSG00000149054.15","gene_symbol":"ZNF215","gene_name":"zinc finger protein 215 [Source:HGNC Symbol;Acc:HGNC:13007]","synonyms":"ZSCAN43,ZKSCAN11","biotype":"protein_coding","ncbi_id":"7762","summary":"This gene is imprinted in a tissue-specific manner with preferential expression in the testis, and encodes a zinc finger protein that belongs to a family of zinc finger transcription factors. The encoded protein contains an N-terminal SRE-ZBP, Ctfin51, AW-1, and Number 18 (SCAN) domain, a kruppel-associated box A (KRABA) domain, and four C-terminal zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017]","start":6926404,"end":7001004,"strand":1,"description":"zinc finger protein 215 [Source:HGNC Symbol;Acc:HGNC:13007]"}, {"versioned_ensembl_gene_id":"ENSG00000227400.2","gene_symbol":"AC012501.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":153421616,"end":153593288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253312.1","gene_symbol":"AC022616.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43251711,"end":43251858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261272.1","gene_symbol":"MUC22","gene_name":"mucin 22 [Source:HGNC Symbol;Acc:HGNC:39755]","synonyms":"PBMUCL1","biotype":"protein_coding","ncbi_id":"100507679","summary":null,"start":31010474,"end":31035402,"strand":1,"description":"mucin 22 [Source:HGNC Symbol;Acc:HGNC:39755]"}, {"versioned_ensembl_gene_id":"ENSG00000184933.5","gene_symbol":"OR6A2","gene_name":"olfactory receptor family 6 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15301]","synonyms":"OR6A2P,OR6A1,OR11-55","biotype":"protein_coding","ncbi_id":"8590","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6791736,"end":6799689,"strand":-1,"description":"olfactory receptor family 6 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15301]"}, {"versioned_ensembl_gene_id":"ENSG00000254781.1","gene_symbol":"AC091564.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6748131,"end":6750324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273344.1","gene_symbol":"PAXIP1-AS1","gene_name":"PAXIP1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27328]","synonyms":null,"biotype":"lincRNA","ncbi_id":"202781","summary":null,"start":155003448,"end":155005703,"strand":1,"description":"PAXIP1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27328]"}, {"versioned_ensembl_gene_id":"ENSG00000262860.5","gene_symbol":"LSM14A","gene_name":"LSM14A, mRNA processing body assembly factor [Source:HGNC Symbol;Acc:HGNC:24489]","synonyms":"RAP55A,RAP55,FAM61A,DKFZP434D1335,C19orf13","biotype":"protein_coding","ncbi_id":"26065","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Mar 2008]","start":34172447,"end":34229322,"strand":1,"description":"LSM14A, mRNA processing body assembly factor [Source:HGNC Symbol;Acc:HGNC:24489]"}, {"versioned_ensembl_gene_id":"ENSG00000259520.5","gene_symbol":"AC051619.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45251580,"end":45279251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262995.1","gene_symbol":"AC137056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20440266,"end":20447000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275906.1","gene_symbol":"AL669830.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30961403,"end":30962396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277318.2","gene_symbol":"IGHV2-5","gene_name":"immunoglobulin heavy variable 2-5 [Source:HGNC Symbol;Acc:HGNC:5576]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28457","summary":null,"start":106038673,"end":106039136,"strand":-1,"description":"immunoglobulin heavy variable 2-5 [Source:HGNC Symbol;Acc:HGNC:5576]"}, {"versioned_ensembl_gene_id":"ENSG00000198881.9","gene_symbol":"ASB12","gene_name":"ankyrin repeat and SOCS box containing 12 [Source:HGNC Symbol;Acc:HGNC:19763]","synonyms":"FLJ39577","biotype":"protein_coding","ncbi_id":"142689","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and a SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. [provided by RefSeq, Jan 2011]","start":64224196,"end":64230631,"strand":-1,"description":"ankyrin repeat and SOCS box containing 12 [Source:HGNC Symbol;Acc:HGNC:19763]"}, {"versioned_ensembl_gene_id":"ENSG00000282678.1","gene_symbol":"AC244226.2","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106025916,"end":106026401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184675.9","gene_symbol":"AMER1","gene_name":"APC membrane recruitment protein 1 [Source:HGNC Symbol;Acc:HGNC:26837]","synonyms":"WTX,RP11-403E24.2,FLJ39827,FAM123B","biotype":"protein_coding","ncbi_id":"139285","summary":"The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS). [provided by RefSeq, May 2010]","start":64185117,"end":64205744,"strand":-1,"description":"APC membrane recruitment protein 1 [Source:HGNC Symbol;Acc:HGNC:26837]"}, {"versioned_ensembl_gene_id":"ENSG00000164303.10","gene_symbol":"ENPP6","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 6 [Source:HGNC Symbol;Acc:HGNC:23409]","synonyms":"MGC33971","biotype":"protein_coding","ncbi_id":"133121","summary":null,"start":184088706,"end":184221230,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 6 [Source:HGNC Symbol;Acc:HGNC:23409]"}, {"versioned_ensembl_gene_id":"ENSG00000250966.2","gene_symbol":"AC023886.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112564988,"end":112565398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251510.1","gene_symbol":"AC022486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18491740,"end":18547698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172888.11","gene_symbol":"ZNF621","gene_name":"zinc finger protein 621 [Source:HGNC Symbol;Acc:HGNC:24787]","synonyms":"FLJ45246","biotype":"protein_coding","ncbi_id":"285268","summary":null,"start":40524878,"end":40574685,"strand":1,"description":"zinc finger protein 621 [Source:HGNC Symbol;Acc:HGNC:24787]"}, {"versioned_ensembl_gene_id":"ENSG00000227403.1","gene_symbol":"LINC01806","gene_name":"long intergenic non-protein coding RNA 1806 [Source:HGNC Symbol;Acc:HGNC:52599]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996579","summary":null,"start":161244739,"end":161249050,"strand":1,"description":"long intergenic non-protein coding RNA 1806 [Source:HGNC Symbol;Acc:HGNC:52599]"}, {"versioned_ensembl_gene_id":"ENSG00000254291.1","gene_symbol":"AC011676.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141326130,"end":141327137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259493.2","gene_symbol":"AC023968.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79559256,"end":79560304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128519.3","gene_symbol":"TAS2R16","gene_name":"taste 2 receptor member 16 [Source:HGNC Symbol;Acc:HGNC:14921]","synonyms":"T2R16","biotype":"protein_coding","ncbi_id":"50833","summary":"This gene encodes a member of a family of candidate taste receptors that are members of the G protein-coupled receptor superfamily. These family members are specifically expressed by taste receptor cells of the tongue and palate epithelia. Each of these apparently intronless genes encodes a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered with another 3 candidate taste receptor genes in chromosome 7 and is genetically linked to loci that influence bitter perception. [provided by RefSeq, Jul 2008]","start":122994704,"end":122995700,"strand":-1,"description":"taste 2 receptor member 16 [Source:HGNC Symbol;Acc:HGNC:14921]"}, {"versioned_ensembl_gene_id":"ENSG00000172534.13","gene_symbol":"HCFC1","gene_name":"host cell factor C1 [Source:HGNC Symbol;Acc:HGNC:4839]","synonyms":"VCAF,PPP1R89,MRX3,MGC70925,HFC1,HCF1,HCF-1,CFF","biotype":"protein_coding","ncbi_id":"3054","summary":"This gene is a member of the host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each of which contains a highly specific cleavage signal. This nuclear coactivator is proteolytically cleaved at one of the six possible sites, resulting in the creation of an N-terminal chain and the corresponding C-terminal chain. The final form of this protein consists of noncovalently bound N- and C-terminal chains. The protein is involved in control of the cell cycle and transcriptional regulation during herpes simplex virus infection. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":153947553,"end":153971807,"strand":-1,"description":"host cell factor C1 [Source:HGNC Symbol;Acc:HGNC:4839]"}, {"versioned_ensembl_gene_id":"ENSG00000178125.14","gene_symbol":"PPP1R42","gene_name":"protein phosphatase 1 regulatory subunit 42 [Source:HGNC Symbol;Acc:HGNC:33732]","synonyms":"TLLR,LRRC67,dtr","biotype":"protein_coding","ncbi_id":"286187","summary":"The protein encoded by this gene can interact with gamma-tubulin and PP1 phosphatase, a regulator of centrosome separation. The encoded protein is a positive regulator of PP1 phosphatase and thus plays a role in the control of centrosome integrity. [provided by RefSeq, Feb 2017]","start":66964099,"end":67056604,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 42 [Source:HGNC Symbol;Acc:HGNC:33732]"}, {"versioned_ensembl_gene_id":"ENSG00000122705.16","gene_symbol":"CLTA","gene_name":"clathrin light chain A [Source:HGNC Symbol;Acc:HGNC:2090]","synonyms":"Lca","biotype":"protein_coding","ncbi_id":"1211","summary":"Clathrin is a large, soluble protein composed of heavy and light chains. It functions as the main structural component of the lattice-type cytoplasmic face of coated pits and vesicles which entrap specific macromolecules during receptor-mediated endocytosis. This gene encodes one of two clathrin light chain proteins which are believed to function as regulatory elements. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 8 and 12. [provided by RefSeq, May 2010]","start":36190856,"end":36304781,"strand":1,"description":"clathrin light chain A [Source:HGNC Symbol;Acc:HGNC:2090]"}, {"versioned_ensembl_gene_id":"ENSG00000168883.19","gene_symbol":"USP39","gene_name":"ubiquitin specific peptidase 39 [Source:HGNC Symbol;Acc:HGNC:20071]","synonyms":"SNRNP65,SAD1,CGI-21","biotype":"protein_coding","ncbi_id":"10713","summary":null,"start":85602856,"end":85649282,"strand":1,"description":"ubiquitin specific peptidase 39 [Source:HGNC Symbol;Acc:HGNC:20071]"}, {"versioned_ensembl_gene_id":"ENSG00000114316.12","gene_symbol":"USP4","gene_name":"ubiquitin specific peptidase 4 [Source:HGNC Symbol;Acc:HGNC:12627]","synonyms":"Unph,UNP","biotype":"protein_coding","ncbi_id":"7375","summary":"The protein encoded by this gene is a protease that deubiquitinates target proteins such as ADORA2A and TRIM21. The encoded protein shuttles between the nucleus and cytoplasm and is involved in maintaining operational fidelity in the endoplasmic reticulum. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":49277831,"end":49340712,"strand":-1,"description":"ubiquitin specific peptidase 4 [Source:HGNC Symbol;Acc:HGNC:12627]"}, {"versioned_ensembl_gene_id":"ENSG00000130695.14","gene_symbol":"CEP85","gene_name":"centrosomal protein 85 [Source:HGNC Symbol;Acc:HGNC:25309]","synonyms":"DKFZP434L0117,CCDC21","biotype":"protein_coding","ncbi_id":"64793","summary":"This gene encodes a protein that belongs to the centrosome-associated family of proteins. The centrosome is a subcellular organelle in the animal cell that functions as a microtubule organizing center and is involved in cell-cycle progression. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":26234153,"end":26279038,"strand":1,"description":"centrosomal protein 85 [Source:HGNC Symbol;Acc:HGNC:25309]"}, {"versioned_ensembl_gene_id":"ENSG00000255112.2","gene_symbol":"CHMP1B","gene_name":"charged multivesicular body protein 1B [Source:HGNC Symbol;Acc:HGNC:24287]","synonyms":"C18orf2,Vps46B,CHMP1.5","biotype":"protein_coding","ncbi_id":"57132","summary":"CHMP1B belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":11851396,"end":11854449,"strand":1,"description":"charged multivesicular body protein 1B [Source:HGNC Symbol;Acc:HGNC:24287]"}, {"versioned_ensembl_gene_id":"ENSG00000282224.1","gene_symbol":"AC243660.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28546431,"end":28546583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176020.8","gene_symbol":"AMIGO3","gene_name":"adhesion molecule with Ig like domain 3 [Source:HGNC Symbol;Acc:HGNC:24075]","synonyms":null,"biotype":"protein_coding","ncbi_id":"386724","summary":null,"start":49716834,"end":49719695,"strand":-1,"description":"adhesion molecule with Ig like domain 3 [Source:HGNC Symbol;Acc:HGNC:24075]"}, {"versioned_ensembl_gene_id":"ENSG00000188782.8","gene_symbol":"CATSPER4","gene_name":"cation channel sperm associated 4 [Source:HGNC Symbol;Acc:HGNC:23220]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378807","summary":null,"start":26190561,"end":26202968,"strand":1,"description":"cation channel sperm associated 4 [Source:HGNC Symbol;Acc:HGNC:23220]"}, {"versioned_ensembl_gene_id":"ENSG00000253307.1","gene_symbol":"AC011676.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141252286,"end":141253292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279974.1","gene_symbol":"AC008739.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20978678,"end":20989626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232991.5","gene_symbol":"GACAT1","gene_name":"gastric cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48336]","synonyms":"LINC00876,AC096655.1-002","biotype":"lincRNA","ncbi_id":"104326057","summary":null,"start":107754112,"end":107822129,"strand":1,"description":"gastric cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48336]"}, {"versioned_ensembl_gene_id":"ENSG00000021762.19","gene_symbol":"OSBPL5","gene_name":"oxysterol binding protein like 5 [Source:HGNC Symbol;Acc:HGNC:16392]","synonyms":"ORP5,KIAA1534","biotype":"protein_coding","ncbi_id":"114879","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors that play a key role in the maintenance of cholesterol balance in the body. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. This gene has been shown to be imprinted, with preferential expression from the maternal allele only in placenta. Transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2010]","start":3087116,"end":3166739,"strand":-1,"description":"oxysterol binding protein like 5 [Source:HGNC Symbol;Acc:HGNC:16392]"}, {"versioned_ensembl_gene_id":"ENSG00000257557.2","gene_symbol":"PPP1R12A-AS1","gene_name":"PPP1R12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51903]","synonyms":"R12A-AS1","biotype":"antisense_RNA","ncbi_id":"105369865","summary":null,"start":79934901,"end":79942712,"strand":1,"description":"PPP1R12A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51903]"}, {"versioned_ensembl_gene_id":"ENSG00000237650.1","gene_symbol":"OR11Q1P","gene_name":"olfactory receptor family 11 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"403227","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131204128,"end":131205004,"strand":1,"description":"olfactory receptor family 11 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31239]"}, {"versioned_ensembl_gene_id":"ENSG00000242193.10","gene_symbol":"AL359075.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":178006136,"end":178037950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180861.9","gene_symbol":"LINC01559","gene_name":"long intergenic non-protein coding RNA 1559 [Source:HGNC Symbol;Acc:HGNC:26598]","synonyms":"FLJ33810,C12orf36","biotype":"lincRNA","ncbi_id":"283422","summary":null,"start":13371089,"end":13387167,"strand":-1,"description":"long intergenic non-protein coding RNA 1559 [Source:HGNC Symbol;Acc:HGNC:26598]"}, {"versioned_ensembl_gene_id":"ENSG00000261557.1","gene_symbol":"AC092725.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27133483,"end":27135179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174953.13","gene_symbol":"DHX36","gene_name":"DEAH-box helicase 36 [Source:HGNC Symbol;Acc:HGNC:14410]","synonyms":"MLEL1,KIAA1488,DDX36","biotype":"protein_coding","ncbi_id":"170506","summary":"This gene is a member of the DEAH-box family of RNA-dependent NTPases which are named after the conserved amino acid sequence Asp-Glu-Ala-His in motif II. The protein encoded by this gene has been shown to enhance the deadenylation and decay of mRNAs with 3'-UTR AU-rich elements (ARE-mRNA). The protein has also been shown to resolve into single strands the highly stable tetramolecular DNA configuration (G4) that can form spontaneously in guanine-rich regions of DNA. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":154272546,"end":154324497,"strand":-1,"description":"DEAH-box helicase 36 [Source:HGNC Symbol;Acc:HGNC:14410]"}, {"versioned_ensembl_gene_id":"ENSG00000100503.23","gene_symbol":"NIN","gene_name":"ninein [Source:HGNC Symbol;Acc:HGNC:14906]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51199","summary":"This gene encodes one of the proteins important for centrosomal function. This protein is important for positioning and anchoring the microtubules minus-ends in epithelial cells. Localization of this protein to the centrosome requires three leucine zippers in the central coiled-coil domain. Multiple alternatively spliced transcript variants that encode different isoforms have been reported. [provided by RefSeq, Jul 2008]","start":50719763,"end":50831121,"strand":-1,"description":"ninein [Source:HGNC Symbol;Acc:HGNC:14906]"}, {"versioned_ensembl_gene_id":"ENSG00000157064.10","gene_symbol":"NMNAT2","gene_name":"nicotinamide nucleotide adenylyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16789]","synonyms":"PNAT2,KIAA0479,C1orf15","biotype":"protein_coding","ncbi_id":"23057","summary":"This gene product belongs to the nicotinamide mononucleotide adenylyltransferase (NMNAT) enzyme family, members of which catalyze an essential step in NAD (NADP) biosynthetic pathway. Unlike the other human family member, which is localized to the nucleus, and is ubiquitously expressed; this enzyme is cytoplasmic, and is predominantly expressed in the brain. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":183248237,"end":183418602,"strand":-1,"description":"nicotinamide nucleotide adenylyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16789]"}, {"versioned_ensembl_gene_id":"ENSG00000237140.2","gene_symbol":"HSPE1P16","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49334]","synonyms":"EPF8","biotype":"processed_pseudogene","ncbi_id":"171421","summary":null,"start":26062750,"end":26063097,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49334]"}, {"versioned_ensembl_gene_id":"ENSG00000119912.15","gene_symbol":"IDE","gene_name":"insulin degrading enzyme [Source:HGNC Symbol;Acc:HGNC:5381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3416","summary":"This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and kallidin. The preferential affinity of this enzyme for insulin results in insulin-mediated inhibition of the degradation of other peptides such as beta-amyloid. Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases. This protein localizes primarily to the cytoplasm but in some cell types localizes to the extracellular space, cell membrane, peroxisome, and mitochondrion. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described but have not been experimentally verified.[provided by RefSeq, Sep 2009]","start":92451684,"end":92574076,"strand":-1,"description":"insulin degrading enzyme [Source:HGNC Symbol;Acc:HGNC:5381]"}, {"versioned_ensembl_gene_id":"ENSG00000236837.1","gene_symbol":"AC139712.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52494688,"end":52500752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068697.6","gene_symbol":"LAPTM4A","gene_name":"lysosomal protein transmembrane 4 alpha [Source:HGNC Symbol;Acc:HGNC:6924]","synonyms":"LAPTM4,KIAA0108,HUMORF13,Mtrp,MBNT","biotype":"protein_coding","ncbi_id":"9741","summary":"This gene encodes a protein that has four predicted transmembrane domains. The function of this gene has not yet been determined; however, studies in the mouse homolog suggest a role in the transport of small molecules across endosomal and lysosomal membranes. [provided by RefSeq, Jul 2008]","start":20032650,"end":20052028,"strand":-1,"description":"lysosomal protein transmembrane 4 alpha [Source:HGNC Symbol;Acc:HGNC:6924]"}, {"versioned_ensembl_gene_id":"ENSG00000234161.1","gene_symbol":"PABPC5-AS1","gene_name":"PABPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31845]","synonyms":"OTTHUMG00000021960,CXorf46","biotype":"antisense_RNA","ncbi_id":"102724167","summary":null,"start":91414878,"end":91434999,"strand":-1,"description":"PABPC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31845]"}, {"versioned_ensembl_gene_id":"ENSG00000281939.1","gene_symbol":"IGHD3-9","gene_name":"immunoglobulin heavy diversity 3-9 [Source:HGNC Symbol;Acc:HGNC:5499]","synonyms":"IGHD39,DXP1","biotype":"IG_D_gene","ncbi_id":"28500","summary":null,"start":105905452,"end":105905482,"strand":-1,"description":"immunoglobulin heavy diversity 3-9 [Source:HGNC Symbol;Acc:HGNC:5499]"}, {"versioned_ensembl_gene_id":"ENSG00000274020.2","gene_symbol":"LINC01138","gene_name":"long intergenic non-protein coding RNA 1138 [Source:HGNC Symbol;Acc:HGNC:49454]","synonyms":"FLJ39739,LINC00875","biotype":"processed_transcript","ncbi_id":"388685","summary":null,"start":148290889,"end":148519604,"strand":-1,"description":"long intergenic non-protein coding RNA 1138 [Source:HGNC Symbol;Acc:HGNC:49454]"}, {"versioned_ensembl_gene_id":"ENSG00000189079.15","gene_symbol":"ARID2","gene_name":"AT-rich interaction domain 2 [Source:HGNC Symbol;Acc:HGNC:18037]","synonyms":"KIAA1557,FLJ30619,DKFZp686G052,BAF200","biotype":"protein_coding","ncbi_id":"196528","summary":"This gene encodes a member of the AT-rich interactive domain (ARID)-containing family of DNA-binding proteins. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and chromatin structure modification. This protein functions as a subunit of the polybromo- and BRG1-associated factor or PBAF (SWI/SNF-B) chromatin remodeling complex which facilitates ligand-dependent transcriptional activation by nuclear receptors. Mutations in this gene are associated with hepatocellular carcinomas. A pseudogene of this gene is found on chromosome1. [provided by RefSeq, Dec 2016]","start":45729665,"end":45908040,"strand":1,"description":"AT-rich interaction domain 2 [Source:HGNC Symbol;Acc:HGNC:18037]"}, {"versioned_ensembl_gene_id":"ENSG00000010810.17","gene_symbol":"FYN","gene_name":"FYN proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4037]","synonyms":"SYN,SLK,MGC45350","biotype":"protein_coding","ncbi_id":"2534","summary":"This gene is a member of the protein-tyrosine kinase oncogene family. It encodes a membrane-associated tyrosine kinase that has been implicated in the control of cell growth. The protein associates with the p85 subunit of phosphatidylinositol 3-kinase and interacts with the fyn-binding protein. Alternatively spliced transcript variants encoding distinct isoforms exist. [provided by RefSeq, Jul 2008]","start":111660332,"end":111873452,"strand":-1,"description":"FYN proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:4037]"}, {"versioned_ensembl_gene_id":"ENSG00000177058.11","gene_symbol":"SLC38A9","gene_name":"solute carrier family 38 member 9 [Source:HGNC Symbol;Acc:HGNC:26907]","synonyms":"FLJ90709","biotype":"protein_coding","ncbi_id":"153129","summary":null,"start":55625845,"end":55773194,"strand":-1,"description":"solute carrier family 38 member 9 [Source:HGNC Symbol;Acc:HGNC:26907]"}, {"versioned_ensembl_gene_id":"ENSG00000259419.2","gene_symbol":"HNRNPCP3","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48815]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646956","summary":null,"start":79236332,"end":79237206,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48815]"}, {"versioned_ensembl_gene_id":"ENSG00000236231.1","gene_symbol":"AC017048.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176524879,"end":176531683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239829.1","gene_symbol":"KRT8P25","gene_name":"keratin 8 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:33377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402134","summary":null,"start":87323268,"end":87324723,"strand":1,"description":"keratin 8 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:33377]"}, {"versioned_ensembl_gene_id":"ENSG00000277530.1","gene_symbol":"DEFB107B","gene_name":"defensin beta 107B [Source:HGNC Symbol;Acc:HGNC:31918]","synonyms":"HsT21816","biotype":"protein_coding","ncbi_id":"503614","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 107, DEFB107A and DEFB107B, in tail-to-tail orientation. This gene, DEFB107B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7487822,"end":7501287,"strand":1,"description":"defensin beta 107B [Source:HGNC Symbol;Acc:HGNC:31918]"}, {"versioned_ensembl_gene_id":"ENSG00000272279.1","gene_symbol":"AL512329.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1528364,"end":1528911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231474.5","gene_symbol":"BX927139.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31055372,"end":31080324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278666.3","gene_symbol":"AC106795.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":177875522,"end":177950732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184911.14","gene_symbol":"DMRTC1B","gene_name":"DMRT like family C1B [Source:HGNC Symbol;Acc:HGNC:31686]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728656","summary":null,"start":72777009,"end":72848802,"strand":1,"description":"DMRT like family C1B [Source:HGNC Symbol;Acc:HGNC:31686]"}, {"versioned_ensembl_gene_id":"ENSG00000168538.15","gene_symbol":"TRAPPC11","gene_name":"trafficking protein particle complex 11 [Source:HGNC Symbol;Acc:HGNC:25751]","synonyms":"gry,foigr,FLJ12716,C4orf41","biotype":"protein_coding","ncbi_id":"60684","summary":"The protein encoded by this gene is a subunit of the TRAPP (transport protein particle) tethering complex, which functions in intracellular vesicle trafficking. This subunit is involved in early stage endoplasmic reticulum-to-Golgi vesicle transport. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":183659267,"end":183713594,"strand":1,"description":"trafficking protein particle complex 11 [Source:HGNC Symbol;Acc:HGNC:25751]"}, {"versioned_ensembl_gene_id":"ENSG00000282909.2","gene_symbol":"AC007241.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18389297,"end":18405046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116721.9","gene_symbol":"PRAMEF1","gene_name":"PRAME family member 1 [Source:HGNC Symbol;Acc:HGNC:28840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65121","summary":"This gene is a member of the PRAME (preferentially expressed antigen of melanoma) gene family which is expressed in many cancers but may function in reproductive tissues during development. Alternative promoter usage generates two transcript variants, which encode different isoforms. [provided by RefSeq, Jun 2014]","start":12791397,"end":12796628,"strand":1,"description":"PRAME family member 1 [Source:HGNC Symbol;Acc:HGNC:28840]"}, {"versioned_ensembl_gene_id":"ENSG00000177699.4","gene_symbol":"AC011944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78978889,"end":78985926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249848.1","gene_symbol":"AC112673.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10336782,"end":10337677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260467.1","gene_symbol":"AC018552.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57681124,"end":57701730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260352.1","gene_symbol":"AC092287.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18926863,"end":18937043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259390.2","gene_symbol":"AC022196.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39512404,"end":39519854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147183.9","gene_symbol":"CPXCR1","gene_name":"CPX chromosome region, candidate 1 [Source:HGNC Symbol;Acc:HGNC:2332]","synonyms":"CT77","biotype":"protein_coding","ncbi_id":"53336","summary":"This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]","start":88747225,"end":88754785,"strand":1,"description":"CPX chromosome region, candidate 1 [Source:HGNC Symbol;Acc:HGNC:2332]"}, {"versioned_ensembl_gene_id":"ENSG00000259269.1","gene_symbol":"AC109630.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39472703,"end":39481206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250796.1","gene_symbol":"AC112484.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128869624,"end":128870026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261159.1","gene_symbol":"AC112484.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128859716,"end":128860526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058335.15","gene_symbol":"RASGRF1","gene_name":"Ras protein specific guanine nucleotide releasing factor 1 [Source:HGNC Symbol;Acc:HGNC:9875]","synonyms":"PP13187,H-GRF55,GRF55,GRF1,GNRP,CDC25L,CDC25","biotype":"protein_coding","ncbi_id":"5923","summary":"The protein encoded by this gene is a guanine nucleotide exchange factor (GEF) similar to the Saccharomyces cerevisiae CDC25 gene product. Functional analysis has demonstrated that this protein stimulates the dissociation of GDP from RAS protein. The studies of the similar gene in mouse suggested that the Ras-GEF activity of this protein in brain can be activated by Ca2+ influx, muscarinic receptors, and G protein beta-gamma subunit. Mouse studies also indicated that the Ras-GEF signaling pathway mediated by this protein may be important for long-term memory. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Mar 2009]","start":78959947,"end":79090773,"strand":-1,"description":"Ras protein specific guanine nucleotide releasing factor 1 [Source:HGNC Symbol;Acc:HGNC:9875]"}, {"versioned_ensembl_gene_id":"ENSG00000243022.1","gene_symbol":"MARK3P3","gene_name":"microtubule affinity regulating kinase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50314]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533754","summary":null,"start":128848673,"end":128849399,"strand":-1,"description":"microtubule affinity regulating kinase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50314]"}, {"versioned_ensembl_gene_id":"ENSG00000276130.4","gene_symbol":"SLC22A18","gene_name":"solute carrier family 22 member 18 [Source:HGNC Symbol;Acc:HGNC:10964]","synonyms":"BWR1A,TSSC5,SLC22A1L,ORCTL2,ITM,IMPT1,BWSCR1A","biotype":"protein_coding","ncbi_id":"5002","summary":"This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015]","start":2899745,"end":2925175,"strand":1,"description":"solute carrier family 22 member 18 [Source:HGNC Symbol;Acc:HGNC:10964]"}, {"versioned_ensembl_gene_id":"ENSG00000198690.9","gene_symbol":"FAN1","gene_name":"FANCD2 and FANCI associated nuclease 1 [Source:HGNC Symbol;Acc:HGNC:29170]","synonyms":"MTMR15,KIAA1018,MTMR15,KIAA1018","biotype":"protein_coding","ncbi_id":"22909","summary":"This gene plays a role in DNA interstrand cross-link repair and encodes a protein with 5' flap endonuclease and 5'-3' exonuclease activity. Mutations in this gene cause karyomegalic interstitial nephritis. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Feb 2016]","start":30903852,"end":30943108,"strand":1,"description":"FANCD2 and FANCI associated nuclease 1 [Source:HGNC Symbol;Acc:HGNC:29170]"}, {"versioned_ensembl_gene_id":"ENSG00000258024.1","gene_symbol":"AC090115.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48385417,"end":48386265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069696.6","gene_symbol":"DRD4","gene_name":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1815","summary":"This gene encodes the D4 subtype of the dopamine receptor. The D4 subtype is a G-protein coupled receptor which inhibits adenylyl cyclase. It is a target for drugs which treat schizophrenia and Parkinson disease. Mutations in this gene have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit/hyperactivity disorder, and the personality trait of novelty seeking. This gene contains a polymorphic number (2-10 copies) of tandem 48 nt repeats; the sequence shown contains four repeats. [provided by RefSeq, Jul 2008]","start":637293,"end":640706,"strand":1,"description":"dopamine receptor D4 [Source:HGNC Symbol;Acc:HGNC:3025]"}, {"versioned_ensembl_gene_id":"ENSG00000276099.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54698377,"end":54700905,"strand":-1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000232176.1","gene_symbol":"AL161909.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19200335,"end":19201046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000018408.14","gene_symbol":"WWTR1","gene_name":"WW domain containing transcription regulator 1 [Source:HGNC Symbol;Acc:HGNC:24042]","synonyms":"TAZ,DKFZp586I1419","biotype":"protein_coding","ncbi_id":"25937","summary":null,"start":149517235,"end":149736714,"strand":-1,"description":"WW domain containing transcription regulator 1 [Source:HGNC Symbol;Acc:HGNC:24042]"}, {"versioned_ensembl_gene_id":"ENSG00000241985.1","gene_symbol":"WWTR1-IT1","gene_name":"WWTR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41469]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478977","summary":null,"start":149648997,"end":149650184,"strand":-1,"description":"WWTR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41469]"}, {"versioned_ensembl_gene_id":"ENSG00000223668.1","gene_symbol":"EEF1A1P24","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645715","summary":null,"start":39358545,"end":39359922,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:37897]"}, {"versioned_ensembl_gene_id":"ENSG00000276816.2","gene_symbol":"PRAMEF22","gene_name":"PRAME family member 22 [Source:HGNC Symbol;Acc:HGNC:34393]","synonyms":"PRAMEF3L","biotype":"unprocessed_pseudogene","ncbi_id":"653606","summary":null,"start":13093633,"end":13098515,"strand":1,"description":"PRAME family member 22 [Source:HGNC Symbol;Acc:HGNC:34393]"}, {"versioned_ensembl_gene_id":"ENSG00000272694.1","gene_symbol":"Z94160.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37371684,"end":37372858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275172.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724485,"end":54736504,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000180304.14","gene_symbol":"OAZ2","gene_name":"ornithine decarboxylase antizyme 2 [Source:HGNC Symbol;Acc:HGNC:8096]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4947","summary":"The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamines. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 2, the second member of the antizyme family. Like antizyme 1, antizyme 2 has broad tissue distribution, inhibits ODC activity and polyamine uptake, and stimulates ODC degradation in vivo; however, it fails to promote ODC degradation in vitro. Antizyme 2 is expressed at lower levels than antizyme 1, but is evolutionary more conserved, suggesting it likely has an important biological role. Studies also show different subcellular localization of antizymes 1 and 2, indicating specific function for each antizyme in discrete compartments of the cell. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014]","start":64687573,"end":64703281,"strand":-1,"description":"ornithine decarboxylase antizyme 2 [Source:HGNC Symbol;Acc:HGNC:8096]"}, {"versioned_ensembl_gene_id":"ENSG00000279875.1","gene_symbol":"AC074029.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48189349,"end":48191207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214894.6","gene_symbol":"LINC00243","gene_name":"long intergenic non-protein coding RNA 243 [Source:HGNC Symbol;Acc:HGNC:30956]","synonyms":"NCRNA00243,FLJ40693,C6orf214,bQB230F21.2,bQB10J12.2","biotype":"lincRNA","ncbi_id":"401247","summary":null,"start":30798654,"end":30830659,"strand":-1,"description":"long intergenic non-protein coding RNA 243 [Source:HGNC Symbol;Acc:HGNC:30956]"}, {"versioned_ensembl_gene_id":"ENSG00000276503.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"transcribed_processed_pseudogene","ncbi_id":"554300","summary":null,"start":54763222,"end":54775570,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000240131.1","gene_symbol":"AL049829.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23229961,"end":23230116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280786.1","gene_symbol":"BX544879.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46187101,"end":46190209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076003.4","gene_symbol":"MCM6","gene_name":"minichromosome maintenance complex component 6 [Source:HGNC Symbol;Acc:HGNC:6949]","synonyms":"Mis5","biotype":"protein_coding","ncbi_id":"4175","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 4 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of the complex by CDC2 kinase reduces the helicase activity, suggesting a role in the regulation of DNA replication. Single nucleotide polymorphisms in the intron regions of this gene are associated with differential transcriptional activation of the promoter of the neighboring lactase gene and, thereby, influence lactose intolerance in early adulthood. [provided by RefSeq, May 2012]","start":135839626,"end":135876426,"strand":-1,"description":"minichromosome maintenance complex component 6 [Source:HGNC Symbol;Acc:HGNC:6949]"}, {"versioned_ensembl_gene_id":"ENSG00000227050.1","gene_symbol":"AL512288.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27938875,"end":27960193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215368.5","gene_symbol":"BOD1P2","gene_name":"biorientation of chromosomes in cell division 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51436]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129355","summary":null,"start":5132749,"end":5133229,"strand":-1,"description":"biorientation of chromosomes in cell division 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51436]"}, {"versioned_ensembl_gene_id":"ENSG00000229138.1","gene_symbol":"CDY6P","gene_name":"chromodomain Y-linked 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:23853]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386730","summary":null,"start":17882099,"end":17883708,"strand":-1,"description":"chromodomain Y-linked 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:23853]"}, {"versioned_ensembl_gene_id":"ENSG00000162636.15","gene_symbol":"FAM102B","gene_name":"family with sequence similarity 102 member B [Source:HGNC Symbol;Acc:HGNC:27637]","synonyms":"SYM-3B,DKFZp779B126","biotype":"protein_coding","ncbi_id":"284611","summary":null,"start":108560089,"end":108644900,"strand":1,"description":"family with sequence similarity 102 member B [Source:HGNC Symbol;Acc:HGNC:27637]"}, {"versioned_ensembl_gene_id":"ENSG00000278061.2","gene_symbol":"MT2P1","gene_name":"metallothionein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7407]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"4503","summary":null,"start":68376327,"end":68376509,"strand":1,"description":"metallothionein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7407]"}, {"versioned_ensembl_gene_id":"ENSG00000183663.6","gene_symbol":"AC007992.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96068729,"end":96069681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282195.1","gene_symbol":"SORD2P","gene_name":"sorbitol dehydrogenase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49919]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653381","summary":null,"start":44827352,"end":44893221,"strand":-1,"description":"sorbitol dehydrogenase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49919]"}, {"versioned_ensembl_gene_id":"ENSG00000223555.1","gene_symbol":"USP9YP23","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:38759]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100500798","summary":null,"start":17782210,"end":17784815,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:38759]"}, {"versioned_ensembl_gene_id":"ENSG00000235665.5","gene_symbol":"LINC00298","gene_name":"long intergenic non-protein coding RNA 298 [Source:HGNC Symbol;Acc:HGNC:49257]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339788","summary":null,"start":7922425,"end":8278084,"strand":-1,"description":"long intergenic non-protein coding RNA 298 [Source:HGNC Symbol;Acc:HGNC:49257]"}, {"versioned_ensembl_gene_id":"ENSG00000242703.1","gene_symbol":"CCT4P1","gene_name":"chaperonin containing TCP1 subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"650172","summary":null,"start":140997952,"end":140999800,"strand":-1,"description":"chaperonin containing TCP1 subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35151]"}, {"versioned_ensembl_gene_id":"ENSG00000067715.13","gene_symbol":"SYT1","gene_name":"synaptotagmin 1 [Source:HGNC Symbol;Acc:HGNC:11509]","synonyms":"SYT,SVP65,P65","biotype":"protein_coding","ncbi_id":"6857","summary":"The synaptotagmins are integral membrane proteins of synaptic vesicles thought to serve as Ca(2+) sensors in the process of vesicular trafficking and exocytosis. Calcium binding to synaptotagmin-1 participates in triggering neurotransmitter release at the synapse (Fernandez-Chacon et al., 2001 [PubMed 11242035]).[supplied by OMIM, Jul 2010]","start":78863993,"end":79452008,"strand":1,"description":"synaptotagmin 1 [Source:HGNC Symbol;Acc:HGNC:11509]"}, {"versioned_ensembl_gene_id":"ENSG00000140905.10","gene_symbol":"GCSH","gene_name":"glycine cleavage system protein H [Source:HGNC Symbol;Acc:HGNC:4208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2653","summary":"Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.[provided by RefSeq, Jan 2010]","start":81081938,"end":81096425,"strand":-1,"description":"glycine cleavage system protein H [Source:HGNC Symbol;Acc:HGNC:4208]"}, {"versioned_ensembl_gene_id":"ENSG00000086506.2","gene_symbol":"HBQ1","gene_name":"hemoglobin subunit theta 1 [Source:HGNC Symbol;Acc:HGNC:4833]","synonyms":"HBQ","biotype":"protein_coding","ncbi_id":"3049","summary":"Theta-globin mRNA is found in human fetal erythroid tissue but not in adult erythroid or other nonerythroid tissue. The theta-1 gene may be expressed very early in embryonic life, perhaps sometime before 5 weeks. Theta-1 is a member of the human alpha-globin gene cluster that involves five functional genes and two pseudogenes. The order of genes is: 5' - zeta - pseudozeta - mu - pseudoalpha-2 -pseudoalpha-1 - alpha-2 - alpha-1 - theta-1 - 3'. Research supports a transcriptionally active role for the gene and a functional role for the peptide in specific cells, possibly those of early erythroid tissue. [provided by RefSeq, Jul 2008]","start":180453,"end":181181,"strand":1,"description":"hemoglobin subunit theta 1 [Source:HGNC Symbol;Acc:HGNC:4833]"}, {"versioned_ensembl_gene_id":"ENSG00000106086.18","gene_symbol":"PLEKHA8","gene_name":"pleckstrin homology domain containing A8 [Source:HGNC Symbol;Acc:HGNC:30037]","synonyms":"MGC3358,FAPP2","biotype":"protein_coding","ncbi_id":"84725","summary":null,"start":30027404,"end":30130483,"strand":1,"description":"pleckstrin homology domain containing A8 [Source:HGNC Symbol;Acc:HGNC:30037]"}, {"versioned_ensembl_gene_id":"ENSG00000211793.2","gene_symbol":"TRAV9-2","gene_name":"T-cell receptor alpha variable 9-2 [Source:HGNC Symbol;Acc:HGNC:12154]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28677","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21941128,"end":21941657,"strand":1,"description":"T-cell receptor alpha variable 9-2 [Source:HGNC Symbol;Acc:HGNC:12154]"}, {"versioned_ensembl_gene_id":"ENSG00000100350.14","gene_symbol":"FOXRED2","gene_name":"FAD dependent oxidoreductase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26264]","synonyms":"FLJ23322,ERFAD","biotype":"protein_coding","ncbi_id":"80020","summary":null,"start":36487190,"end":36507101,"strand":-1,"description":"FAD dependent oxidoreductase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26264]"}, {"versioned_ensembl_gene_id":"ENSG00000228665.2","gene_symbol":"BX679664.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109030067,"end":109030319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232944.1","gene_symbol":"AC092423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56408699,"end":56409210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133878.8","gene_symbol":"DUSP26","gene_name":"dual specificity phosphatase 26 [Source:HGNC Symbol;Acc:HGNC:28161]","synonyms":"MGC1136,DUSP24","biotype":"protein_coding","ncbi_id":"78986","summary":"This gene encodes a member of the tyrosine phosphatase family of proteins and exhibits dual specificity by dephosphorylating tyrosine as well as serine and threonine residues. This gene has been described as both a tumor suppressor and an oncogene depending on the cellular context. This protein may regulate neuronal proliferation and has been implicated in the progression of glioblastoma through its ability to dephosphorylate the p53 tumor suppressor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":33591332,"end":33600106,"strand":-1,"description":"dual specificity phosphatase 26 [Source:HGNC Symbol;Acc:HGNC:28161]"}, {"versioned_ensembl_gene_id":"ENSG00000232361.3","gene_symbol":"AC069304.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150614061,"end":150614764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224370.1","gene_symbol":"AC093392.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56380976,"end":56381312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282915.1","gene_symbol":"AC091769.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":72467749,"end":72473304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226636.1","gene_symbol":"AC006020.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122159300,"end":122162243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225421.2","gene_symbol":"AC019330.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198493242,"end":198772356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204053.6","gene_symbol":"MYCLP1","gene_name":"MYCL pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7556]","synonyms":"MYCL2,MYCL1P1","biotype":"processed_pseudogene","ncbi_id":"4611","summary":null,"start":107272582,"end":107273656,"strand":1,"description":"MYCL pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7556]"}, {"versioned_ensembl_gene_id":"ENSG00000258064.1","gene_symbol":"AC073612.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71674204,"end":71698968,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140612.13","gene_symbol":"SEC11A","gene_name":"SEC11 homolog A, signal peptidase complex subunit [Source:HGNC Symbol;Acc:HGNC:17718]","synonyms":"SPCS4A,SPC18,sid2895,SEC11L1","biotype":"protein_coding","ncbi_id":"23478","summary":"This gene encodes a member of the peptidase S26B family. The encoded protein is an 18kDa subunit of the signal peptidase complex and has been linked to cell migration and invasion, gastric cancer and lymph node metastasis. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, Dec 2012]","start":84669538,"end":84716716,"strand":-1,"description":"SEC11 homolog A, signal peptidase complex subunit [Source:HGNC Symbol;Acc:HGNC:17718]"}, {"versioned_ensembl_gene_id":"ENSG00000275074.1","gene_symbol":"NUDT18","gene_name":"nudix hydrolase 18 [Source:HGNC Symbol;Acc:HGNC:26194]","synonyms":"MTH3,FLJ22494","biotype":"protein_coding","ncbi_id":"79873","summary":"The protein encoded by this gene is a member of the Nudix hydrolase family. Nudix hydrolases eliminate potentially toxic nucleotide metabolites from the cell and regulate the concentrations and availability of many different nucleotide substrates, cofactors, and signaling molecules. This protein contains a Nudix hydrolase domain and hydrolyzes oxidized forms of guanosine and deoxyguanosine diphosphates. [provided by RefSeq, Sep 2012]","start":22106872,"end":22109419,"strand":-1,"description":"nudix hydrolase 18 [Source:HGNC Symbol;Acc:HGNC:26194]"}, {"versioned_ensembl_gene_id":"ENSG00000158525.15","gene_symbol":"CPA5","gene_name":"carboxypeptidase A5 [Source:HGNC Symbol;Acc:HGNC:15722]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93979","summary":"Carboxypeptidases have functions ranging from digestion of food to selective biosynthesis of neuroendocrine peptides. Members of the A/B subfamily of carboxypeptidases, such as CPA5, contain an approximately 90-amino acid pro region that assists in the folding of the active carboxypeptidase domain. Cleavage of the pro region activates the enzyme (Wei et al., 2002 [PubMed 11836249]).[supplied by OMIM, Mar 2008]","start":130344816,"end":130368730,"strand":1,"description":"carboxypeptidase A5 [Source:HGNC Symbol;Acc:HGNC:15722]"}, {"versioned_ensembl_gene_id":"ENSG00000233588.1","gene_symbol":"CYP51A1P2","gene_name":"cytochrome P450 family 51 subfamily A member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20251]","synonyms":"CYP51P2","biotype":"processed_pseudogene","ncbi_id":"83530","summary":null,"start":28722386,"end":28724021,"strand":-1,"description":"cytochrome P450 family 51 subfamily A member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20251]"}, {"versioned_ensembl_gene_id":"ENSG00000272375.1","gene_symbol":"AC026979.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30197404,"end":30198048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197416.4","gene_symbol":"FABP12","gene_name":"fatty acid binding protein 12 [Source:HGNC Symbol;Acc:HGNC:34524]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646486","summary":null,"start":81524981,"end":81531378,"strand":-1,"description":"fatty acid binding protein 12 [Source:HGNC Symbol;Acc:HGNC:34524]"}, {"versioned_ensembl_gene_id":"ENSG00000280769.1","gene_symbol":"AL732314.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":418137,"end":420960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275079.3","gene_symbol":"LPCAT1","gene_name":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]","synonyms":"FLJ12443,AYTL2,AGPAT9,AGPAT10","biotype":"protein_coding","ncbi_id":"79888","summary":"This gene encodes a member of the 1-acyl-sn-glycerol-3-phosphate acyltransferase family of proteins. The encoded enzyme plays a role in phospholipid metabolism, specifically in the conversion of lysophosphatidylcholine to phosphatidylcholine in the presence of acyl-CoA. This process is important in the synthesis of lung surfactant and platelet-activating factor (PAF). Elevated expression of this gene may contribute to the progression of oral squamous cell, prostate, breast, and other human cancers. [provided by RefSeq, Sep 2016]","start":1460716,"end":1505839,"strand":-1,"description":"lysophosphatidylcholine acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:25718]"}, {"versioned_ensembl_gene_id":"ENSG00000281032.1","gene_symbol":"FAM181A-AS1","gene_name":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]","synonyms":"C14orf86","biotype":"antisense_RNA","ncbi_id":"283592","summary":null,"start":93904730,"end":93927066,"strand":-1,"description":"FAM181A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20133]"}, {"versioned_ensembl_gene_id":"ENSG00000228786.5","gene_symbol":"LINC00266-4P","gene_name":"long intergenic non-protein coding RNA 266-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:38800]","synonyms":"NCRNA00266Y2,NCRNA00266D,NCRNA00266-4P","biotype":"lincRNA","ncbi_id":"100642176","summary":null,"start":25378300,"end":25394719,"strand":-1,"description":"long intergenic non-protein coding RNA 266-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:38800]"}, {"versioned_ensembl_gene_id":"ENSG00000260896.5","gene_symbol":"LINC02170","gene_name":"long intergenic non-protein coding RNA 2170 [Source:HGNC Symbol;Acc:HGNC:53032]","synonyms":"PRCAT47","biotype":"lincRNA","ncbi_id":"100996425","summary":null,"start":80828735,"end":80892595,"strand":-1,"description":"long intergenic non-protein coding RNA 2170 [Source:HGNC Symbol;Acc:HGNC:53032]"}, {"versioned_ensembl_gene_id":"ENSG00000229648.1","gene_symbol":"RPSAP22","gene_name":"ribosomal protein SA pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36435]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270874","summary":null,"start":85490930,"end":85491780,"strand":-1,"description":"ribosomal protein SA pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36435]"}, {"versioned_ensembl_gene_id":"ENSG00000147003.5","gene_symbol":"TMEM27","gene_name":"transmembrane protein 27 [Source:HGNC Symbol;Acc:HGNC:29437]","synonyms":"NX17","biotype":"protein_coding","ncbi_id":"57393","summary":"This gene encodes a type 1 transmembrane protein that is important for trafficking amino acid transporters to the apical brush border of proximal tubules. The encoded protein binds to amino acid transporters and regulates their expression on the plasma membrane. It also plays a role in controlling insulin exocytosis by regulating formation of the SNARE (soluble N-ethylmaleimide-sensitive-factor attachment protein receptor) complex in pancreatic beta cells. The extracellular domain of the encoded protein may be cleaved and shed from the plasma membrane specifically in pancreatic beta cells. [provided by RefSeq, Jun 2013]","start":15627318,"end":15665031,"strand":-1,"description":"transmembrane protein 27 [Source:HGNC Symbol;Acc:HGNC:29437]"}, {"versioned_ensembl_gene_id":"ENSG00000135902.9","gene_symbol":"CHRND","gene_name":"cholinergic receptor nicotinic delta subunit [Source:HGNC Symbol;Acc:HGNC:1965]","synonyms":"ACHRD","biotype":"protein_coding","ncbi_id":"1144","summary":"The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":232525993,"end":232536667,"strand":1,"description":"cholinergic receptor nicotinic delta subunit [Source:HGNC Symbol;Acc:HGNC:1965]"}, {"versioned_ensembl_gene_id":"ENSG00000234174.1","gene_symbol":"AC016683.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113171535,"end":113175360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251445.1","gene_symbol":"AC021151.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169010430,"end":169010939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177300.6","gene_symbol":"CLDN22","gene_name":"claudin 22 [Source:HGNC Symbol;Acc:HGNC:2044]","synonyms":"CLDN21","biotype":"protein_coding","ncbi_id":"53842","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is intronless and overlaps the 3' UTR of the WWC2 gene (GeneID: 80014) on the opposite strand. [provided by RefSeq, Aug 2010]","start":183318194,"end":183320774,"strand":-1,"description":"claudin 22 [Source:HGNC Symbol;Acc:HGNC:2044]"}, {"versioned_ensembl_gene_id":"ENSG00000138613.13","gene_symbol":"APH1B","gene_name":"aph-1 homolog B, gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:24080]","synonyms":"PSFL,DKFZp564D0372,APH-1B","biotype":"protein_coding","ncbi_id":"83464","summary":"This gene encodes a multi-pass transmembrane protein that is a functional component of the gamma-secretase complex, which also contains presenilin and nicastrin. This protein represents a stabilizing cofactor for the presenilin holoprotein in the complex. The gamma-secretase complex catalyzes the cleavage of integral proteins such as notch receptors and beta-amyloid precursor protein. [provided by RefSeq, Sep 2011]","start":63276018,"end":63309126,"strand":1,"description":"aph-1 homolog B, gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:24080]"}, {"versioned_ensembl_gene_id":"ENSG00000238250.1","gene_symbol":"ST6GAL2-IT1","gene_name":"ST6GAL2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41380]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874354","summary":null,"start":106822923,"end":106825031,"strand":-1,"description":"ST6GAL2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41380]"}, {"versioned_ensembl_gene_id":"ENSG00000234332.1","gene_symbol":"BCAS2P2","gene_name":"BCAS2, pre-mRNA processing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39595]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421045","summary":null,"start":100393033,"end":100394026,"strand":-1,"description":"BCAS2, pre-mRNA processing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39595]"}, {"versioned_ensembl_gene_id":"ENSG00000278429.3","gene_symbol":"GOLGA8DP","gene_name":"golgin A8 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32376]","synonyms":"GOLGA8D","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132979","summary":null,"start":22429756,"end":22440620,"strand":-1,"description":"golgin A8 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32376]"}, {"versioned_ensembl_gene_id":"ENSG00000223695.1","gene_symbol":"FO393418.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36388626,"end":36396517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211785.1","gene_symbol":"TRAV12-1","gene_name":"T-cell receptor alpha variable 12-1 [Source:HGNC Symbol;Acc:HGNC:12105]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28674","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21841240,"end":21841774,"strand":1,"description":"T-cell receptor alpha variable 12-1 [Source:HGNC Symbol;Acc:HGNC:12105]"}, {"versioned_ensembl_gene_id":"ENSG00000224631.4","gene_symbol":"RPS27AP16","gene_name":"ribosomal protein S27a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36855]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"643358","summary":null,"start":61055399,"end":61055964,"strand":-1,"description":"ribosomal protein S27a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36855]"}, {"versioned_ensembl_gene_id":"ENSG00000141627.13","gene_symbol":"DYM","gene_name":"dymeclin [Source:HGNC Symbol;Acc:HGNC:21317]","synonyms":"SMC,FLJ20071,DMC","biotype":"protein_coding","ncbi_id":"54808","summary":"This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]","start":49041474,"end":49461347,"strand":-1,"description":"dymeclin [Source:HGNC Symbol;Acc:HGNC:21317]"}, {"versioned_ensembl_gene_id":"ENSG00000237666.2","gene_symbol":"AC097527.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106470799,"end":106477669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255556.2","gene_symbol":"AC087203.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12378679,"end":12380265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261773.1","gene_symbol":"AC244090.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":154517840,"end":154518631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102078.15","gene_symbol":"SLC25A14","gene_name":"solute carrier family 25 member 14 [Source:HGNC Symbol;Acc:HGNC:10984]","synonyms":"UCP5,BMCP1","biotype":"protein_coding","ncbi_id":"9016","summary":"Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). Uncoupling proteins separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. Uncoupling proteins facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. This gene is widely expressed in many tissues with the greatest abundance in brain and testis. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on chromosome 4. [provided by RefSeq, Aug 2013]","start":130339888,"end":130373361,"strand":1,"description":"solute carrier family 25 member 14 [Source:HGNC Symbol;Acc:HGNC:10984]"}, {"versioned_ensembl_gene_id":"ENSG00000281537.1","gene_symbol":"AC136687.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22374469,"end":22376303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049246.14","gene_symbol":"PER3","gene_name":"period circadian clock 3 [Source:HGNC Symbol;Acc:HGNC:8847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8863","summary":"This gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene have been linked to sleep disorders. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2014]","start":7784320,"end":7845177,"strand":1,"description":"period circadian clock 3 [Source:HGNC Symbol;Acc:HGNC:8847]"}, {"versioned_ensembl_gene_id":"ENSG00000112115.5","gene_symbol":"IL17A","gene_name":"interleukin 17A [Source:HGNC Symbol;Acc:HGNC:5981]","synonyms":"IL17,IL-17A,IL-17,CTLA8","biotype":"protein_coding","ncbi_id":"3605","summary":"This gene is a member of the IL-17 receptor family which includes five members (IL-17RA-E) and the encoded protein is a proinflammatory cytokine produced by activated T cells. IL-17A-mediated downstream pathways induce the production of inflammatory molecules, chemokines, antimicrobial peptides, and remodeling proteins. The encoded protein elicits crucial impacts on host defense, cell trafficking, immune modulation, and tissue repair, with a key role in the induction of innate immune defenses. This cytokine stimulates non-hematopoietic cells and promotes chemokine production thereby attracting myeloid cells to inflammatory sites. This cytokine also regulates the activities of NF-kappaB and mitogen-activated protein kinases and can stimulate the expression of IL6 and cyclooxygenase-2 (PTGS2/COX-2), as well as enhance the production of nitric oxide (NO). IL-17A plays a pivotal role in various infectious diseases, inflammatory and autoimmune disorders, and cancer. High levels of this cytokine are associated with several chronic inflammatory diseases including rheumatoid arthritis, psoriasis and multiple sclerosis. The lung damage induced by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is to a large extent, a result of the inflammatory response promoted by cytokines such as IL17A. [provided by RefSeq, Sep 2020]","start":52186387,"end":52190638,"strand":1,"description":"interleukin 17A [Source:HGNC Symbol;Acc:HGNC:5981]"}, {"versioned_ensembl_gene_id":"ENSG00000234940.1","gene_symbol":"AC023128.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144688413,"end":144690185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266604.1","gene_symbol":"LINC01887","gene_name":"long intergenic non-protein coding RNA 1887 [Source:HGNC Symbol;Acc:HGNC:52706]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724470","summary":null,"start":10612304,"end":10626353,"strand":-1,"description":"long intergenic non-protein coding RNA 1887 [Source:HGNC Symbol;Acc:HGNC:52706]"}, {"versioned_ensembl_gene_id":"ENSG00000264503.1","gene_symbol":"AP001180.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10622123,"end":10622267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271938.1","gene_symbol":"AC103724.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42139461,"end":42139752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049247.13","gene_symbol":"UTS2","gene_name":"urotensin 2 [Source:HGNC Symbol;Acc:HGNC:12636]","synonyms":"PRO1068,UII,UCN2,U-II","biotype":"protein_coding","ncbi_id":"10911","summary":"This gene encodes a mature peptide that is an active cyclic heptapeptide absolutely conserved from lamprey to human. The active peptide acts as a vasoconstrictor and is expressed only in brain tissue. Despite the gene family name similarity, this gene is not homologous to urocortin, a member of the sauvagine/corticotropin-releasing factor/urotensin I family. Most of the proprotein is cleaved to make the mature peptide. Transcript variants encoding different preproprotein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":7843083,"end":7853512,"strand":-1,"description":"urotensin 2 [Source:HGNC Symbol;Acc:HGNC:12636]"}, {"versioned_ensembl_gene_id":"ENSG00000075886.10","gene_symbol":"TUBA3D","gene_name":"tubulin alpha 3d [Source:HGNC Symbol;Acc:HGNC:24071]","synonyms":"H2-ALPHA","biotype":"protein_coding","ncbi_id":"113457","summary":"This gene encodes a member of the alpha tubulin family. Tubulin is a major component of microtubules, which are composed of alpha- and beta-tubulin heterodimers and microtubule-associated proteins in the cytoskeleton. Microtubules maintain cellular structure, function in intracellular transport, and play a role in spindle formation during mitosis. [provided by RefSeq, Oct 2011]","start":131476093,"end":131482934,"strand":1,"description":"tubulin alpha 3d [Source:HGNC Symbol;Acc:HGNC:24071]"}, {"versioned_ensembl_gene_id":"ENSG00000117586.10","gene_symbol":"TNFSF4","gene_name":"TNF superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:11934]","synonyms":"TXGP1,OX-40L,gp34,CD252","biotype":"protein_coding","ncbi_id":"7292","summary":"This gene encodes a cytokine of the tumor necrosis factor (TNF) ligand family. The encoded protein functions in T cell antigen-presenting cell (APC) interactions and mediates adhesion of activated T cells to endothelial cells. Polymorphisms in this gene have been associated with Sjogren's syndrome and systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":173183734,"end":173207313,"strand":-1,"description":"TNF superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:11934]"}, {"versioned_ensembl_gene_id":"ENSG00000169592.14","gene_symbol":"INO80E","gene_name":"INO80 complex subunit E [Source:HGNC Symbol;Acc:HGNC:26905]","synonyms":"FLJ90652,CCDC95","biotype":"protein_coding","ncbi_id":"283899","summary":null,"start":29995294,"end":30005793,"strand":1,"description":"INO80 complex subunit E [Source:HGNC Symbol;Acc:HGNC:26905]"}, {"versioned_ensembl_gene_id":"ENSG00000180152.3","gene_symbol":"XIAPP3","gene_name":"X-linked inhibitor of apoptosis pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128413","summary":null,"start":112853328,"end":112854122,"strand":1,"description":"X-linked inhibitor of apoptosis pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52377]"}, {"versioned_ensembl_gene_id":"ENSG00000205653.1","gene_symbol":"AL035696.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":203313,"end":206392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241754.1","gene_symbol":"AC108748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102663163,"end":102673913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261889.1","gene_symbol":"AC108134.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3156736,"end":3157483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275703.1","gene_symbol":"U47924.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6899752,"end":6900212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227357.2","gene_symbol":"HLA-DRB4","gene_name":"major histocompatibility complex, class II, DR beta 4 [Source:HGNC Symbol;Acc:HGNC:4952]","synonyms":"HLA-DR4B,HLA-DR4B","biotype":"protein_coding","ncbi_id":"3126","summary":"HLA-DRB4 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32542598,"end":32557561,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 4 [Source:HGNC Symbol;Acc:HGNC:4952]"}, {"versioned_ensembl_gene_id":"ENSG00000237119.1","gene_symbol":"LINC01056","gene_name":"long intergenic non-protein coding RNA 1056 [Source:HGNC Symbol;Acc:HGNC:49050]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100144597","summary":null,"start":63038011,"end":63053863,"strand":1,"description":"long intergenic non-protein coding RNA 1056 [Source:HGNC Symbol;Acc:HGNC:49050]"}, {"versioned_ensembl_gene_id":"ENSG00000253214.1","gene_symbol":"AC079209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81154279,"end":81164599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271385.1","gene_symbol":"AL161798.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91464578,"end":91464708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114544.16","gene_symbol":"SLC41A3","gene_name":"solute carrier family 41 member 3 [Source:HGNC Symbol;Acc:HGNC:31046]","synonyms":"FLJ20473","biotype":"protein_coding","ncbi_id":"54946","summary":null,"start":126006355,"end":126101561,"strand":-1,"description":"solute carrier family 41 member 3 [Source:HGNC Symbol;Acc:HGNC:31046]"}, {"versioned_ensembl_gene_id":"ENSG00000273820.1","gene_symbol":"USP27X","gene_name":"ubiquitin specific peptidase 27, X-linked [Source:HGNC Symbol;Acc:HGNC:13486]","synonyms":"USP27","biotype":"protein_coding","ncbi_id":"389856","summary":"This gene encodes a member of the peptidase protein family. The encoded protein functions as a deubiquitinase that is involved in upregulation of the pro-apoptotic Bim protein. This protein may act as a tumor suppressor by increasing levels of Bim to counteract anti-apoptotic signals in cancer cells. Mutations in this gene have been associated with X-linked cognitive disability. [provided by RefSeq, Dec 2016]","start":49879948,"end":49882565,"strand":1,"description":"ubiquitin specific peptidase 27, X-linked [Source:HGNC Symbol;Acc:HGNC:13486]"}, {"versioned_ensembl_gene_id":"ENSG00000261520.5","gene_symbol":"DLGAP1-AS5","gene_name":"DLGAP1 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:27586]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"284215","summary":null,"start":4264602,"end":4295405,"strand":1,"description":"DLGAP1 antisense RNA 5 [Source:HGNC Symbol;Acc:HGNC:27586]"}, {"versioned_ensembl_gene_id":"ENSG00000284041.1","gene_symbol":"AC073111.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":150368790,"end":150396915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240238.1","gene_symbol":"AC092754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59552615,"end":59553093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257128.1","gene_symbol":"AC006197.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41911256,"end":41912212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226831.1","gene_symbol":"MED15P3","gene_name":"mediator complex subunit 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48652]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481657","summary":null,"start":131395217,"end":131395542,"strand":-1,"description":"mediator complex subunit 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48652]"}, {"versioned_ensembl_gene_id":"ENSG00000187630.15","gene_symbol":"DHRS4L2","gene_name":"dehydrogenase/reductase 4 like 2 [Source:HGNC Symbol;Acc:HGNC:19731]","synonyms":"SDR25C3","biotype":"protein_coding","ncbi_id":"317749","summary":"This gene encodes a member of the short chain dehydrogenase reductase family. The encoded protein may be an NADPH dependent retinol oxidoreductase. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":23969874,"end":24006408,"strand":1,"description":"dehydrogenase/reductase 4 like 2 [Source:HGNC Symbol;Acc:HGNC:19731]"}, {"versioned_ensembl_gene_id":"ENSG00000215256.3","gene_symbol":"DHRS4-AS1","gene_name":"DHRS4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23175]","synonyms":"PRO1488,C14orf167,AS1DHRS4","biotype":"antisense_RNA","ncbi_id":"55449","summary":null,"start":23938731,"end":23988839,"strand":-1,"description":"DHRS4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23175]"}, {"versioned_ensembl_gene_id":"ENSG00000088992.17","gene_symbol":"TESC","gene_name":"tescalcin [Source:HGNC Symbol;Acc:HGNC:26065]","synonyms":"FLJ20607,CHP3,TSC","biotype":"protein_coding","ncbi_id":"54997","summary":null,"start":117038923,"end":117099479,"strand":-1,"description":"tescalcin [Source:HGNC Symbol;Acc:HGNC:26065]"}, {"versioned_ensembl_gene_id":"ENSG00000237686.6","gene_symbol":"AL109615.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43995723,"end":44074652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227775.3","gene_symbol":"AL031282.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":1724512,"end":1737251,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229401.1","gene_symbol":"MIR5689HG","gene_name":"MIR5689 host gene [Source:HGNC Symbol;Acc:HGNC:52007]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106660610","summary":null,"start":10434316,"end":10456781,"strand":1,"description":"MIR5689 host gene [Source:HGNC Symbol;Acc:HGNC:52007]"}, {"versioned_ensembl_gene_id":"ENSG00000125735.10","gene_symbol":"TNFSF14","gene_name":"TNF superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11930]","synonyms":"LTg,LIGHT,HVEM-L,CD258","biotype":"protein_coding","ncbi_id":"8740","summary":"The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry mediator (HVEM). This protein may function as a costimulatory factor for the activation of lymphoid cells and as a deterrent to infection by herpesvirus. This protein has been shown to stimulate the proliferation of T cells, and trigger apoptosis of various tumor cells. This protein is also reported to prevent tumor necrosis factor alpha mediated apoptosis in primary hepatocyte. Two alternatively spliced transcript variant encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":6661253,"end":6670588,"strand":-1,"description":"TNF superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11930]"}, {"versioned_ensembl_gene_id":"ENSG00000135436.8","gene_symbol":"FAM186B","gene_name":"family with sequence similarity 186 member B [Source:HGNC Symbol;Acc:HGNC:25296]","synonyms":"DKFZP434J0113,C12orf25","biotype":"protein_coding","ncbi_id":"84070","summary":"This gene product is a member of the FAM186 family, however, its exact function is not known. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":49582885,"end":49605639,"strand":-1,"description":"family with sequence similarity 186 member B [Source:HGNC Symbol;Acc:HGNC:25296]"}, {"versioned_ensembl_gene_id":"ENSG00000224242.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1,BTL-II","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32401346,"end":32414522,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000236590.1","gene_symbol":"MTATP6P4","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44578]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480797","summary":null,"start":131380916,"end":131381590,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44578]"}, {"versioned_ensembl_gene_id":"ENSG00000157429.15","gene_symbol":"ZNF19","gene_name":"zinc finger protein 19 [Source:HGNC Symbol;Acc:HGNC:12981]","synonyms":"MGC51021,KOX12","biotype":"protein_coding","ncbi_id":"7567","summary":"The protein encoded by this gene contains a zinc finger, a nucleic acid-binding domain present in many transcription factors. This gene is located in a region next to ZNF23, a gene also encoding a zinc finger protein, on chromosome 16. [provided by RefSeq, Jul 2008]","start":71464555,"end":71565089,"strand":-1,"description":"zinc finger protein 19 [Source:HGNC Symbol;Acc:HGNC:12981]"}, {"versioned_ensembl_gene_id":"ENSG00000279699.1","gene_symbol":"AC004264.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30275215,"end":30276951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173253.15","gene_symbol":"DMRT2","gene_name":"doublesex and mab-3 related transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:2935]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10655","summary":"The protein encoded by this gene belongs to the DMRT gene family, sharing a DM DNA-binding domain with Drosophila 'doublesex' (dsx) and C. elegans mab3, genes involved in sex determination in these organisms. Also, this gene is located in a region of the human genome (chromosome 9p24.3) associated with gonadal dysgenesis and XY sex reversal. Hence this gene is one of the candidates for sex-determining gene(s) on chr 9. [provided by RefSeq, Apr 2010]","start":1049858,"end":1057552,"strand":1,"description":"doublesex and mab-3 related transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:2935]"}, {"versioned_ensembl_gene_id":"ENSG00000146904.8","gene_symbol":"EPHA1","gene_name":"EPH receptor A1 [Source:HGNC Symbol;Acc:HGNC:3385]","synonyms":"EPHT1,EPHT,EPH","biotype":"protein_coding","ncbi_id":"2041","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene is expressed in some human cancer cell lines and has been implicated in carcinogenesis. [provided by RefSeq, Jul 2008]","start":143390289,"end":143408892,"strand":-1,"description":"EPH receptor A1 [Source:HGNC Symbol;Acc:HGNC:3385]"}, {"versioned_ensembl_gene_id":"ENSG00000167377.17","gene_symbol":"ZNF23","gene_name":"zinc finger protein 23 [Source:HGNC Symbol;Acc:HGNC:13023]","synonyms":"KOX16,ZNF612,ZNF359,Zfp612","biotype":"protein_coding","ncbi_id":"7571","summary":null,"start":71447597,"end":71463095,"strand":-1,"description":"zinc finger protein 23 [Source:HGNC Symbol;Acc:HGNC:13023]"}, {"versioned_ensembl_gene_id":"ENSG00000179388.8","gene_symbol":"EGR3","gene_name":"early growth response 3 [Source:HGNC Symbol;Acc:HGNC:3240]","synonyms":"PILOT","biotype":"protein_coding","ncbi_id":"1960","summary":"This gene encodes a transcriptional regulator that belongs to the EGR family of C2H2-type zinc-finger proteins. It is an immediate-early growth response gene which is induced by mitogenic stimulation. The protein encoded by this gene participates in the transcriptional regulation of genes in controling biological rhythm. It may also play a role in a wide variety of processes including muscle development, lymphocyte development, endothelial cell growth and migration, and neuronal development. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2010]","start":22687659,"end":22693302,"strand":-1,"description":"early growth response 3 [Source:HGNC Symbol;Acc:HGNC:3240]"}, {"versioned_ensembl_gene_id":"ENSG00000233609.3","gene_symbol":"RPL10P19","gene_name":"ribosomal protein L10 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52350]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645960","summary":null,"start":8961200,"end":8979025,"strand":1,"description":"ribosomal protein L10 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52350]"}, {"versioned_ensembl_gene_id":"ENSG00000282245.1","gene_symbol":"AC100797.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":738548,"end":740374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284138.1","gene_symbol":"AC099795.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42952202,"end":42952641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185236.11","gene_symbol":"RAB11B","gene_name":"RAB11B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9761]","synonyms":"H-YPT3","biotype":"protein_coding","ncbi_id":"9230","summary":"The Ras superfamily of small GTP-binding proteins, which includes the Ras (see MIM 190020), Ral (see MIM 179550), Rho (see MIM 165390), Rap (see MIM 179520), and Rab (see MIM 179508) families, is involved in controlling a diverse set of essential cellular functions. The Rab family, including RAB11B, appears to play a critical role in regulating exocytotic and endocytotic pathways (summary by Zhu et al., 1994 [PubMed 7811277]).[supplied by OMIM, Nov 2010]","start":8389981,"end":8404434,"strand":1,"description":"RAB11B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9761]"}, {"versioned_ensembl_gene_id":"ENSG00000275265.1","gene_symbol":"AC127002.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122501187,"end":122501641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262896.2","gene_symbol":"KRTAP9-4","gene_name":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]","synonyms":"KAP9.4","biotype":"protein_coding","ncbi_id":"85280","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41238317,"end":41239283,"strand":1,"description":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]"}, {"versioned_ensembl_gene_id":"ENSG00000279629.1","gene_symbol":"AC048380.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48661840,"end":48662635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261348.1","gene_symbol":"LINC02136","gene_name":"long intergenic non-protein coding RNA 2136 [Source:HGNC Symbol;Acc:HGNC:52995]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371333","summary":null,"start":71410440,"end":71426464,"strand":-1,"description":"long intergenic non-protein coding RNA 2136 [Source:HGNC Symbol;Acc:HGNC:52995]"}, {"versioned_ensembl_gene_id":"ENSG00000231795.1","gene_symbol":"ITCH-IT1","gene_name":"ITCH intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41397]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874302","summary":null,"start":34450930,"end":34454552,"strand":1,"description":"ITCH intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41397]"}, {"versioned_ensembl_gene_id":"ENSG00000232558.1","gene_symbol":"KCND3-IT1","gene_name":"KCND3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41350]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874295","summary":null,"start":111853762,"end":111856905,"strand":-1,"description":"KCND3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41350]"}, {"versioned_ensembl_gene_id":"ENSG00000277214.1","gene_symbol":"AC009159.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79603572,"end":79604177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278742.3","gene_symbol":"LRRC37A","gene_name":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]","synonyms":"KIAA0563,KIAA0563","biotype":"protein_coding","ncbi_id":"9884","summary":null,"start":45723122,"end":45768499,"strand":-1,"description":"leucine rich repeat containing 37A [Source:HGNC Symbol;Acc:HGNC:29069]"}, {"versioned_ensembl_gene_id":"ENSG00000089091.16","gene_symbol":"DZANK1","gene_name":"double zinc ribbon and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:15858]","synonyms":"FLJ30892,FLJ10600,dJ568F9.2,C20orf84,C20orf12,bA189K21.8,ANKRD64","biotype":"protein_coding","ncbi_id":"55184","summary":"This gene contains two ankyrin repeat-encoding regions. Ankyrin repeats are tandemly repeated modules of about 33 amino acids described as L-shaped structures consisting of a beta-hairpin and two alpha-helices. Ankyrin repeats occur in a large number of functionally diverse proteins, mainly from eukaryotes, and are known to function as protein-protein interaction domains. [provided by RefSeq, Dec 2018]","start":18383367,"end":18467281,"strand":-1,"description":"double zinc ribbon and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:15858]"}, {"versioned_ensembl_gene_id":"ENSG00000240244.3","gene_symbol":"GAPDHP33","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:37785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644237","summary":null,"start":119596167,"end":119597179,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:37785]"}, {"versioned_ensembl_gene_id":"ENSG00000234244.1","gene_symbol":"AL512641.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18746433,"end":18747853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250215.1","gene_symbol":"CIR1P2","gene_name":"corepressor interacting with RBPJ, 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131828","summary":null,"start":114713579,"end":114714920,"strand":-1,"description":"corepressor interacting with RBPJ, 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44012]"}, {"versioned_ensembl_gene_id":"ENSG00000225509.1","gene_symbol":"AIFM1P1","gene_name":"apoptosis inducing factor, mitochondria associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44884]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645120","summary":null,"start":18735745,"end":18738631,"strand":1,"description":"apoptosis inducing factor, mitochondria associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44884]"}, {"versioned_ensembl_gene_id":"ENSG00000235391.1","gene_symbol":"CR753841.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32507110,"end":32508241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236675.1","gene_symbol":"MTX1P1","gene_name":"metaxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7505]","synonyms":"MTXP,MTX1P","biotype":"unprocessed_pseudogene","ncbi_id":"4581","summary":null,"start":155230975,"end":155234325,"strand":1,"description":"metaxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7505]"}, {"versioned_ensembl_gene_id":"ENSG00000203799.12","gene_symbol":"CCDC162P","gene_name":"coiled-coil domain containing 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:21565]","synonyms":"CCDC162,C6orf185,C6orf184,bA425D10.7,bA425D10.3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"221262","summary":"This gene is the ortholog of the mouse coiled-coil domain containing 162 gene. This locus is transcribed, but is represented as a unitary pseudogene because there are multiple changes in the coding sequence, including multiple changes that result in premature stop codons, relative to the mouse coding sequence. Transcripts from this locus are expected to encode truncated proteins, and may be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Sep 2018]","start":109165831,"end":109355063,"strand":1,"description":"coiled-coil domain containing 162, pseudogene [Source:HGNC Symbol;Acc:HGNC:21565]"}, {"versioned_ensembl_gene_id":"ENSG00000164011.17","gene_symbol":"ZNF691","gene_name":"zinc finger protein 691 [Source:HGNC Symbol;Acc:HGNC:28028]","synonyms":"Zfp691","biotype":"protein_coding","ncbi_id":"51058","summary":null,"start":42846573,"end":42852477,"strand":1,"description":"zinc finger protein 691 [Source:HGNC Symbol;Acc:HGNC:28028]"}, {"versioned_ensembl_gene_id":"ENSG00000048545.13","gene_symbol":"GUCA1A","gene_name":"guanylate cyclase activator 1A [Source:HGNC Symbol;Acc:HGNC:4678]","synonyms":"GUCA1,GUCA,GCAP1,GCAP,dJ139D8.6,CORD14,COD3,C6orf131","biotype":"protein_coding","ncbi_id":"2978","summary":"This gene encodes an enzyme that plays a role in the recovery of retinal photoreceptors from photobleaching. This enzyme promotes the activity of retinal guanylyl cyclase-1 (GC1) at low calcium concentrations and inhibits GC1 at high calcium concentrations. Mutations in this gene can cause cone dystrophy 3 and code-rod dystrophy 14. provided by RefSeq, Jul 2020]","start":42155406,"end":42180056,"strand":1,"description":"guanylate cyclase activator 1A [Source:HGNC Symbol;Acc:HGNC:4678]"}, {"versioned_ensembl_gene_id":"ENSG00000007080.10","gene_symbol":"CCDC124","gene_name":"coiled-coil domain containing 124 [Source:HGNC Symbol;Acc:HGNC:25171]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115098","summary":null,"start":17933016,"end":17943991,"strand":1,"description":"coiled-coil domain containing 124 [Source:HGNC Symbol;Acc:HGNC:25171]"}, {"versioned_ensembl_gene_id":"ENSG00000108591.9","gene_symbol":"DRG2","gene_name":"developmentally regulated GTP binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3030]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1819","summary":"This gene encodes a GTP-binding protein known to function in the regulation of cell growth and differentiation. Read-through transcripts containing this gene and a downstream gene have been identified, but they are not thought to encode a fusion protein. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jan 2012]","start":18087886,"end":18107971,"strand":1,"description":"developmentally regulated GTP binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3030]"}, {"versioned_ensembl_gene_id":"ENSG00000277223.1","gene_symbol":"AC090116.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71448405,"end":71448850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266677.1","gene_symbol":"AC087164.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18172625,"end":18184753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277491.1","gene_symbol":"AC087392.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":795306,"end":795794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091542.8","gene_symbol":"ALKBH5","gene_name":"alkB homolog 5, RNA demethylase [Source:HGNC Symbol;Acc:HGNC:25996]","synonyms":"OFOXD1,FLJ20308","biotype":"protein_coding","ncbi_id":"54890","summary":null,"start":18183078,"end":18209954,"strand":1,"description":"alkB homolog 5, RNA demethylase [Source:HGNC Symbol;Acc:HGNC:25996]"}, {"versioned_ensembl_gene_id":"ENSG00000273180.1","gene_symbol":"AC019193.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183075480,"end":183076033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171094.17","gene_symbol":"ALK","gene_name":"ALK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:427]","synonyms":"CD246","biotype":"protein_coding","ncbi_id":"238","summary":"This gene encodes a receptor tyrosine kinase, which belongs to the insulin receptor superfamily. This protein comprises an extracellular domain, an hydrophobic stretch corresponding to a single pass transmembrane region, and an intracellular kinase domain. It plays an important role in the development of the brain and exerts its effects on specific neurons in the nervous system. This gene has been found to be rearranged, mutated, or amplified in a series of tumours including anaplastic large cell lymphomas, neuroblastoma, and non-small cell lung cancer. The chromosomal rearrangements are the most common genetic alterations in this gene, which result in creation of multiple fusion genes in tumourigenesis, including ALK (chromosome 2)/EML4 (chromosome 2), ALK/RANBP2 (chromosome 2), ALK/ATIC (chromosome 2), ALK/TFG (chromosome 3), ALK/NPM1 (chromosome 5), ALK/SQSTM1 (chromosome 5), ALK/KIF5B (chromosome 10), ALK/CLTC (chromosome 17), ALK/TPM4 (chromosome 19), and ALK/MSN (chromosome X).[provided by RefSeq, Jan 2011]","start":29192774,"end":29921566,"strand":-1,"description":"ALK receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:427]"}, {"versioned_ensembl_gene_id":"ENSG00000282813.1","gene_symbol":"ARMC10","gene_name":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]","synonyms":"SVH,MGC3195","biotype":"protein_coding","ncbi_id":"83787","summary":"This gene encodes a protein that contains an armadillo repeat and transmembrane domain. The encoded protein decreases the transcriptional activity of the tumor suppressor protein p53 through direct interaction with the DNA-binding domain of p53, and may play a role in cell growth and survival. Upregulation of this gene may play a role in hepatocellular carcinoma. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Sep 2011]","start":103086630,"end":103099764,"strand":1,"description":"armadillo repeat containing 10 [Source:HGNC Symbol;Acc:HGNC:21706]"}, {"versioned_ensembl_gene_id":"ENSG00000260897.1","gene_symbol":"DNM1P30","gene_name":"dynamin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35177]","synonyms":"DNM1DN4@,DNM1DN4-3,DNM1DN3@,DNM1DN3-4","biotype":"unprocessed_pseudogene","ncbi_id":"728388","summary":null,"start":30150872,"end":30153409,"strand":-1,"description":"dynamin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35177]"}, {"versioned_ensembl_gene_id":"ENSG00000270342.1","gene_symbol":"AL499605.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106544342,"end":106544744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236935.1","gene_symbol":"AP003774.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64325050,"end":64329504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224860.1","gene_symbol":"GXYLT1P2","gene_name":"glucoside xylosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39677]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441958","summary":null,"start":13824406,"end":13825635,"strand":-1,"description":"glucoside xylosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39677]"}, {"versioned_ensembl_gene_id":"ENSG00000227950.1","gene_symbol":"AL590128.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6834333,"end":6834618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249069.7","gene_symbol":"LINC01033","gene_name":"long intergenic non-protein coding RNA 1033 [Source:HGNC Symbol;Acc:HGNC:49019]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355136","summary":null,"start":54320944,"end":54415125,"strand":1,"description":"long intergenic non-protein coding RNA 1033 [Source:HGNC Symbol;Acc:HGNC:49019]"}, {"versioned_ensembl_gene_id":"ENSG00000213144.2","gene_symbol":"AC084880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119194850,"end":119195394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226203.1","gene_symbol":"LINC01733","gene_name":"long intergenic non-protein coding RNA 1733 [Source:HGNC Symbol;Acc:HGNC:52521]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926955","summary":null,"start":25955812,"end":25969288,"strand":1,"description":"long intergenic non-protein coding RNA 1733 [Source:HGNC Symbol;Acc:HGNC:52521]"}, {"versioned_ensembl_gene_id":"ENSG00000241449.5","gene_symbol":"AC092666.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150040521,"end":150076655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224016.2","gene_symbol":"AC092681.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149891191,"end":149909704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151790.8","gene_symbol":"TDO2","gene_name":"tryptophan 2,3-dioxygenase [Source:HGNC Symbol;Acc:HGNC:11708]","synonyms":"TPH2,TDO","biotype":"protein_coding","ncbi_id":"6999","summary":"This gene encodes a heme enzyme that plays a critical role in tryptophan metabolism by catalyzing the first and rate-limiting step of the kynurenine pathway. Increased activity of the encoded protein and subsequent kynurenine production may also play a role in cancer through the suppression of antitumor immune responses, and single nucleotide polymorphisms in this gene may be associated with autism. [provided by RefSeq, Feb 2012]","start":155854738,"end":155920406,"strand":1,"description":"tryptophan 2,3-dioxygenase [Source:HGNC Symbol;Acc:HGNC:11708]"}, {"versioned_ensembl_gene_id":"ENSG00000260470.1","gene_symbol":"AC023794.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54145069,"end":54147225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226688.6","gene_symbol":"ENTPD1-AS1","gene_name":"ENTPD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45203]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"728558","summary":null,"start":95753206,"end":96090238,"strand":-1,"description":"ENTPD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45203]"}, {"versioned_ensembl_gene_id":"ENSG00000230300.1","gene_symbol":"STARD13-IT1","gene_name":"STARD13 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41453]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874373","summary":null,"start":33158587,"end":33164409,"strand":-1,"description":"STARD13 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41453]"}, {"versioned_ensembl_gene_id":"ENSG00000151090.17","gene_symbol":"THRB","gene_name":"thyroid hormone receptor beta [Source:HGNC Symbol;Acc:HGNC:11799]","synonyms":"THRB1,THR1,PRTH,NR1A2,GRTH,ERBA2,ERBA-BETA,THRB2","biotype":"protein_coding","ncbi_id":"7068","summary":"The protein encoded by this gene is a nuclear hormone receptor for triiodothyronine. It is one of the several receptors for thyroid hormone, and has been shown to mediate the biological activities of thyroid hormone. Knockout studies in mice suggest that the different receptors, while having certain extent of redundancy, may mediate different functions of thyroid hormone. Mutations in this gene are known to be a cause of generalized thyroid hormone resistance (GTHR), a syndrome characterized by goiter and high levels of circulating thyroid hormone (T3-T4), with normal or slightly elevated thyroid stimulating hormone (TSH). Several alternatively spliced transcript variants encoding the same protein have been observed for this gene. [provided by RefSeq, Jul 2008]","start":24117160,"end":24495282,"strand":-1,"description":"thyroid hormone receptor beta [Source:HGNC Symbol;Acc:HGNC:11799]"}, {"versioned_ensembl_gene_id":"ENSG00000225173.1","gene_symbol":"AL662890.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28837869,"end":28839006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237630.1","gene_symbol":"NIFKP9","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44957]","synonyms":"MKI67IPP9","biotype":"processed_pseudogene","ncbi_id":"106480805","summary":null,"start":127170011,"end":127170231,"strand":1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44957]"}, {"versioned_ensembl_gene_id":"ENSG00000228593.1","gene_symbol":"CFTRP1","gene_name":"cystic fibrosis transmembrane conductance regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16182]","synonyms":"dJ760C5.1,C20orf189","biotype":"unprocessed_pseudogene","ncbi_id":"140871","summary":null,"start":25919499,"end":25919681,"strand":-1,"description":"cystic fibrosis transmembrane conductance regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16182]"}, {"versioned_ensembl_gene_id":"ENSG00000272094.1","gene_symbol":"AC091614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90860550,"end":90862920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234584.1","gene_symbol":"AC019186.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157725708,"end":157736005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000003137.8","gene_symbol":"CYP26B1","gene_name":"cytochrome P450 family 26 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:20581]","synonyms":"P450RAI-2","biotype":"protein_coding","ncbi_id":"56603","summary":"This gene encodes a member of the cytochrome P450 superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein is localized to the endoplasmic reticulum, and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms. Mutations in this gene are associated with radiohumeral fusions and other skeletal and craniofacial anomalies, and increased levels of the encoded protein are associated with atherosclerotic lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":72129238,"end":72148038,"strand":-1,"description":"cytochrome P450 family 26 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:20581]"}, {"versioned_ensembl_gene_id":"ENSG00000231910.1","gene_symbol":"GAMTP2","gene_name":"guanidinoacetate N-methyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129452","summary":null,"start":34574204,"end":34574666,"strand":-1,"description":"guanidinoacetate N-methyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37697]"}, {"versioned_ensembl_gene_id":"ENSG00000271901.1","gene_symbol":"AL161716.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34545929,"end":34671182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276328.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724453,"end":54736091,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000240857.1","gene_symbol":"RDH14","gene_name":"retinol dehydrogenase 14 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:19979]","synonyms":"SDR7C4,PAN2","biotype":"protein_coding","ncbi_id":"57665","summary":null,"start":18554723,"end":18560680,"strand":-1,"description":"retinol dehydrogenase 14 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:19979]"}, {"versioned_ensembl_gene_id":"ENSG00000226465.1","gene_symbol":"AL390198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25751218,"end":25752761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281901.1","gene_symbol":"AC233280.18","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204175.5","gene_symbol":"GPRIN2","gene_name":"G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:HGNC:23730]","synonyms":"MGC15171,KIAA0514","biotype":"protein_coding","ncbi_id":"9721","summary":null,"start":46549044,"end":46555530,"strand":-1,"description":"G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:HGNC:23730]"}, {"versioned_ensembl_gene_id":"ENSG00000246350.1","gene_symbol":"AL049543.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28587378,"end":28591747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143882.10","gene_symbol":"ATP6V1C2","gene_name":"ATPase H+ transporting V1 subunit C2 [Source:HGNC Symbol;Acc:HGNC:18264]","synonyms":"VMA5,ATP6C2","biotype":"protein_coding","ncbi_id":"245973","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A,three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. This gene encodes alternate transcriptional splice variants, encoding different V1 domain C subunit isoforms. [provided by RefSeq, Jul 2008]","start":10721649,"end":10785110,"strand":1,"description":"ATPase H+ transporting V1 subunit C2 [Source:HGNC Symbol;Acc:HGNC:18264]"}, {"versioned_ensembl_gene_id":"ENSG00000124227.5","gene_symbol":"ANKRD60","gene_name":"ankyrin repeat domain 60 [Source:HGNC Symbol;Acc:HGNC:16217]","synonyms":"C20orf86,bA196N14.3","biotype":"protein_coding","ncbi_id":"140731","summary":null,"start":58218495,"end":58228653,"strand":-1,"description":"ankyrin repeat domain 60 [Source:HGNC Symbol;Acc:HGNC:16217]"}, {"versioned_ensembl_gene_id":"ENSG00000276417.1","gene_symbol":"AC092111.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8205984,"end":8207397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146842.16","gene_symbol":"TMEM209","gene_name":"transmembrane protein 209 [Source:HGNC Symbol;Acc:HGNC:21898]","synonyms":"FLJ14803,NET31","biotype":"protein_coding","ncbi_id":"84928","summary":null,"start":130164715,"end":130207770,"strand":-1,"description":"transmembrane protein 209 [Source:HGNC Symbol;Acc:HGNC:21898]"}, {"versioned_ensembl_gene_id":"ENSG00000229611.1","gene_symbol":"AL354707.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6704471,"end":6707780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214405.3","gene_symbol":"RAP1BP2","gene_name":"RAP1B, member of RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128179","summary":null,"start":104063039,"end":104063582,"strand":1,"description":"RAP1B, member of RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49781]"}, {"versioned_ensembl_gene_id":"ENSG00000257635.2","gene_symbol":"CR383656.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18698639,"end":18699978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132912.12","gene_symbol":"DCTN4","gene_name":"dynactin subunit 4 [Source:HGNC Symbol;Acc:HGNC:15518]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51164","summary":null,"start":150708440,"end":150759109,"strand":-1,"description":"dynactin subunit 4 [Source:HGNC Symbol;Acc:HGNC:15518]"}, {"versioned_ensembl_gene_id":"ENSG00000240230.5","gene_symbol":"COX19","gene_name":"COX19, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:28074]","synonyms":"MGC104475","biotype":"protein_coding","ncbi_id":"90639","summary":"COX19 encodes a cytochrome c oxidase (COX)-assembly protein. The S. cerevisiae Cox19 protein may play a role in metal transport to the mitochondrial intermembrane space and assembly of complex IV of the mitochondrial respiratory chain (Sacconi et al., 2005 [PubMed 16212937]).[supplied by OMIM, Mar 2008]","start":898778,"end":975599,"strand":-1,"description":"COX19, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:28074]"}, {"versioned_ensembl_gene_id":"ENSG00000189366.9","gene_symbol":"ALG1L","gene_name":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase like [Source:HGNC Symbol;Acc:HGNC:33721]","synonyms":"ALG1L1","biotype":"protein_coding","ncbi_id":"200810","summary":null,"start":125929275,"end":125937039,"strand":-1,"description":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase like [Source:HGNC Symbol;Acc:HGNC:33721]"}, {"versioned_ensembl_gene_id":"ENSG00000244025.4","gene_symbol":"KRTAP19-3","gene_name":"keratin associated protein 19-3 [Source:HGNC Symbol;Acc:HGNC:18938]","synonyms":"KAP19.3","biotype":"protein_coding","ncbi_id":"337970","summary":null,"start":30491464,"end":30491985,"strand":-1,"description":"keratin associated protein 19-3 [Source:HGNC Symbol;Acc:HGNC:18938]"}, {"versioned_ensembl_gene_id":"ENSG00000186965.4","gene_symbol":"KRTAP19-2","gene_name":"keratin associated protein 19-2 [Source:HGNC Symbol;Acc:HGNC:18937]","synonyms":"KAP19.2","biotype":"protein_coding","ncbi_id":"337969","summary":null,"start":30487057,"end":30487436,"strand":-1,"description":"keratin associated protein 19-2 [Source:HGNC Symbol;Acc:HGNC:18937]"}, {"versioned_ensembl_gene_id":"ENSG00000254274.1","gene_symbol":"TDGF1P5","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:11705]","synonyms":"TDGF5,CRIPTO-5,CR-5","biotype":"processed_pseudogene","ncbi_id":"22814","summary":null,"start":54073114,"end":54073566,"strand":1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:11705]"}, {"versioned_ensembl_gene_id":"ENSG00000171084.15","gene_symbol":"FAM86JP","gene_name":"family with sequence similarity 86 member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:44097]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100125556","summary":null,"start":125916620,"end":125930024,"strand":1,"description":"family with sequence similarity 86 member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:44097]"}, {"versioned_ensembl_gene_id":"ENSG00000264230.7","gene_symbol":"ANXA8L1","gene_name":"annexin A8 like 1 [Source:HGNC Symbol;Acc:HGNC:23334]","synonyms":"bA301J7.3,bA145E20.2,ANXA8L2","biotype":"protein_coding","ncbi_id":"728113","summary":"This gene encodes a member of the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins. The encoded protein may function as an an anticoagulant that indirectly inhibits the thromboplastin-specific complex. Overexpression of this gene has been associated with acute myelocytic leukemia. A highly similar duplicated copy of this gene is found in close proximity on the long arm of chromosome 10. [provided by RefSeq, Apr 2014]","start":46375627,"end":46537864,"strand":1,"description":"annexin A8 like 1 [Source:HGNC Symbol;Acc:HGNC:23334]"}, {"versioned_ensembl_gene_id":"ENSG00000240241.5","gene_symbol":"AC108752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78266940,"end":78294731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225381.2","gene_symbol":"RPS5P7","gene_name":"ribosomal protein S5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36881]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392520","summary":null,"start":109853312,"end":109853919,"strand":1,"description":"ribosomal protein S5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36881]"}, {"versioned_ensembl_gene_id":"ENSG00000260853.1","gene_symbol":"AC109460.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28956687,"end":28966883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244346.1","gene_symbol":"AC092953.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182950783,"end":182956307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229389.2","gene_symbol":"AC111152.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30052942,"end":30073064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236048.2","gene_symbol":"AC013470.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12471352,"end":12472545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254719.1","gene_symbol":"AC080023.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10272052,"end":10272259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258076.1","gene_symbol":"CR383656.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18645991,"end":18646503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257731.2","gene_symbol":"CR383656.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18645044,"end":18646221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235877.1","gene_symbol":"BX294158.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30349200,"end":30349833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248824.2","gene_symbol":"AC108078.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69406931,"end":69407655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250106.1","gene_symbol":"ANKRD33B-AS1","gene_name":"ANKRD33B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41298]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874247","summary":null,"start":10627260,"end":10628225,"strand":-1,"description":"ANKRD33B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41298]"}, {"versioned_ensembl_gene_id":"ENSG00000168621.14","gene_symbol":"GDNF","gene_name":"glial cell derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:4232]","synonyms":"HFB1-GDNF,ATF2,ATF1","biotype":"protein_coding","ncbi_id":"2668","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The recombinant form of this protein, a highly conserved neurotrophic factor, was shown to promote the survival and differentiation of dopaminergic neurons in culture, and was able to prevent apoptosis of motor neurons induced by axotomy. This protein is a ligand for the product of the RET (rearranged during transfection) protooncogene. Mutations in this gene may be associated with Hirschsprung disease and Tourette syndrome. This gene encodes multiple protein isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]","start":37812677,"end":37839686,"strand":-1,"description":"glial cell derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:4232]"}, {"versioned_ensembl_gene_id":"ENSG00000241592.1","gene_symbol":"AC021074.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142960372,"end":142960543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236542.1","gene_symbol":"MED28P7","gene_name":"mediator complex subunit 28 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45084]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729327","summary":null,"start":25669857,"end":25670386,"strand":-1,"description":"mediator complex subunit 28 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45084]"}, {"versioned_ensembl_gene_id":"ENSG00000279236.1","gene_symbol":"AC064801.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":62551203,"end":62552505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129472.13","gene_symbol":"RAB2B","gene_name":"RAB2B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:20246]","synonyms":"FLJ14824","biotype":"protein_coding","ncbi_id":"84932","summary":"Members of the Rab protein family are nontransforming monomeric GTP-binding proteins of the Ras superfamily that contain 4 highly conserved regions involved in GTP binding and hydrolysis. Rab proteins are prenylated, membrane-bound proteins involved in vesicular fusion and trafficking; see MIM 179508.[supplied by OMIM, Apr 2006]","start":21459020,"end":21476973,"strand":-1,"description":"RAB2B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:20246]"}, {"versioned_ensembl_gene_id":"ENSG00000146530.11","gene_symbol":"VWDE","gene_name":"von Willebrand factor D and EGF domains [Source:HGNC Symbol;Acc:HGNC:21897]","synonyms":"FLJ14712","biotype":"protein_coding","ncbi_id":"221806","summary":null,"start":12330885,"end":12403941,"strand":-1,"description":"von Willebrand factor D and EGF domains [Source:HGNC Symbol;Acc:HGNC:21897]"}, {"versioned_ensembl_gene_id":"ENSG00000130309.10","gene_symbol":"COLGALT1","gene_name":"collagen beta(1-O)galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26182]","synonyms":"GLT25D1,FLJ22329","biotype":"protein_coding","ncbi_id":"79709","summary":"The protein encoded by this gene is one of two enzymes that transfers galactose moieties to hydroxylysine residues of collagen and mannose binding lectin. This gene is constitutively expressed and encodes a soluble protein that localizes to the endoplasmic reticulum. [provided by RefSeq, Dec 2015]","start":17555594,"end":17583162,"strand":1,"description":"collagen beta(1-O)galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26182]"}, {"versioned_ensembl_gene_id":"ENSG00000255966.1","gene_symbol":"AC006064.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6532290,"end":6533498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261638.1","gene_symbol":"AC092378.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58847807,"end":58880213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174939.10","gene_symbol":"ASPHD1","gene_name":"aspartate beta-hydroxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27380]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253982","summary":null,"start":29900375,"end":29919864,"strand":1,"description":"aspartate beta-hydroxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27380]"}, {"versioned_ensembl_gene_id":"ENSG00000260651.1","gene_symbol":"AF213884.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102500841,"end":102501319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251572.2","gene_symbol":"AF213884.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102461250,"end":102462152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267076.1","gene_symbol":"CCDC58P3","gene_name":"coiled-coil domain containing 58 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45026]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"732448","summary":null,"start":12211378,"end":12211807,"strand":1,"description":"coiled-coil domain containing 58 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45026]"}, {"versioned_ensembl_gene_id":"ENSG00000011295.15","gene_symbol":"TTC19","gene_name":"tetratricopeptide repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:26006]","synonyms":"MGC19520,FLJ20343","biotype":"protein_coding","ncbi_id":"54902","summary":"This gene encodes a protein with a tetratricopeptide repeat (TPR) domain containing several TPRs of about 34 aa each. These repeats are found in a variety of organisms including bacteria, fungi and plants, and are involved in a variety of functions including protein-protein interactions. This protein is embedded in the inner mitochondrial membrane and is involved in the formation of the mitochondrial respiratory chain III. It has also been suggested that this protein plays a role in cytokinesis. Mutations in this gene cause mitochondrial complex III deficiency. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2012]","start":15999380,"end":16045015,"strand":1,"description":"tetratricopeptide repeat domain 19 [Source:HGNC Symbol;Acc:HGNC:26006]"}, {"versioned_ensembl_gene_id":"ENSG00000227481.1","gene_symbol":"AC008080.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33730292,"end":33732064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211675.2","gene_symbol":"IGLC1","gene_name":"immunoglobulin lambda constant 1 [Source:HGNC Symbol;Acc:HGNC:5855]","synonyms":"IGLC","biotype":"IG_C_gene","ncbi_id":"3537","summary":null,"start":22895375,"end":22895834,"strand":1,"description":"immunoglobulin lambda constant 1 [Source:HGNC Symbol;Acc:HGNC:5855]"}, {"versioned_ensembl_gene_id":"ENSG00000282816.1","gene_symbol":"AC000035.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29480220,"end":29481113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168374.10","gene_symbol":"ARF4","gene_name":"ADP ribosylation factor 4 [Source:HGNC Symbol;Acc:HGNC:655]","synonyms":"ARF2","biotype":"protein_coding","ncbi_id":"378","summary":"This gene is a member of the human ARF gene family whose members encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The gene products include 5 ARF proteins and 11 ARF-like proteins and constitute one family of the RAS superfamily. The ARF proteins are categorized as class I, class II and class III; this gene is a class II member. The members of each class share a common gene organization. The ARF4 gene spans approximately 12kb and contains six exons and five introns. This gene is the most divergent member of the human ARFs. Conflicting map positions at 3p14 or 3p21 have been reported for this gene. [provided by RefSeq, Jul 2008]","start":57571363,"end":57598220,"strand":-1,"description":"ADP ribosylation factor 4 [Source:HGNC Symbol;Acc:HGNC:655]"}, {"versioned_ensembl_gene_id":"ENSG00000148688.13","gene_symbol":"RPP30","gene_name":"ribonuclease P/MRP subunit p30 [Source:HGNC Symbol;Acc:HGNC:17688]","synonyms":"TSG15","biotype":"protein_coding","ncbi_id":"10556","summary":null,"start":90871716,"end":90908553,"strand":1,"description":"ribonuclease P/MRP subunit p30 [Source:HGNC Symbol;Acc:HGNC:17688]"}, {"versioned_ensembl_gene_id":"ENSG00000073169.13","gene_symbol":"SELENOO","gene_name":"selenoprotein O [Source:HGNC Symbol;Acc:HGNC:30395]","synonyms":"SELO","biotype":"protein_coding","ncbi_id":"83642","summary":"This gene encodes a selenoprotein that is localized to the mitochondria. It is the largest mammalian selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. The exact function of this selenoprotein is not known, but it is thought to have redox activity. [provided by RefSeq, Dec 2016]","start":50200979,"end":50217616,"strand":1,"description":"selenoprotein O [Source:HGNC Symbol;Acc:HGNC:30395]"}, {"versioned_ensembl_gene_id":"ENSG00000237011.1","gene_symbol":"AL357793.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":193684246,"end":193688429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236856.1","gene_symbol":"AC105393.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":388412,"end":416885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111605.16","gene_symbol":"CPSF6","gene_name":"cleavage and polyadenylation specific factor 6 [Source:HGNC Symbol;Acc:HGNC:13871]","synonyms":"HPBRII-7,HPBRII-4,CFIM72,CFIM68,CFIM","biotype":"protein_coding","ncbi_id":"11052","summary":"The protein encoded by this gene is one subunit of a cleavage factor required for 3' RNA cleavage and polyadenylation processing. The interaction of the protein with the RNA is one of the earliest steps in the assembly of the 3' end processing complex and facilitates the recruitment of other processing factors. The cleavage factor complex is composed of four polypeptides. This gene encodes the 68kD subunit. It has a domain organization reminiscent of spliceosomal proteins. [provided by RefSeq, Jul 2008]","start":69239537,"end":69274358,"strand":1,"description":"cleavage and polyadenylation specific factor 6 [Source:HGNC Symbol;Acc:HGNC:13871]"}, {"versioned_ensembl_gene_id":"ENSG00000196981.3","gene_symbol":"WDR5B","gene_name":"WD repeat domain 5B [Source:HGNC Symbol;Acc:HGNC:17826]","synonyms":"FLJ11287","biotype":"protein_coding","ncbi_id":"54554","summary":"This intronless gene encodes a protein containing several WD40 repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, including a trp-asp at the C-terminal end. The encoded protein may mediate protein-protein interactions. [provided by RefSeq, Jul 2008]","start":122412332,"end":122416051,"strand":-1,"description":"WD repeat domain 5B [Source:HGNC Symbol;Acc:HGNC:17826]"}, {"versioned_ensembl_gene_id":"ENSG00000124532.14","gene_symbol":"MRS2","gene_name":"MRS2, magnesium transporter [Source:HGNC Symbol;Acc:HGNC:13785]","synonyms":"MRS2L","biotype":"protein_coding","ncbi_id":"57380","summary":null,"start":24402908,"end":24426194,"strand":1,"description":"MRS2, magnesium transporter [Source:HGNC Symbol;Acc:HGNC:13785]"}, {"versioned_ensembl_gene_id":"ENSG00000261409.1","gene_symbol":"AL035425.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":108719949,"end":108724944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203266.2","gene_symbol":"AL157414.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57114915,"end":57122092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248197.1","gene_symbol":"LINC00290","gene_name":"long intergenic non-protein coding RNA 290 [Source:HGNC Symbol;Acc:HGNC:38515]","synonyms":"NCRNA00290","biotype":"lincRNA","ncbi_id":"728081","summary":null,"start":181064089,"end":181159149,"strand":-1,"description":"long intergenic non-protein coding RNA 290 [Source:HGNC Symbol;Acc:HGNC:38515]"}, {"versioned_ensembl_gene_id":"ENSG00000283202.1","gene_symbol":"AC010149.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":230584815,"end":230586715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254815.5","gene_symbol":"AP006284.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":557595,"end":560107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169398.19","gene_symbol":"PTK2","gene_name":"protein tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:9611]","synonyms":"PPP1R71,FAK1,FAK,FADK","biotype":"protein_coding","ncbi_id":"5747","summary":"This gene encodes a cytoplasmic protein tyrosine kinase which is found concentrated in the focal adhesions that form between cells growing in the presence of extracellular matrix constituents. The encoded protein is a member of the FAK subfamily of protein tyrosine kinases but lacks significant sequence similarity to kinases from other subfamilies. Activation of this gene may be an important early step in cell growth and intracellular signal transduction pathways triggered in response to certain neural peptides or to cell interactions with the extracellular matrix. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2017]","start":140657900,"end":141002216,"strand":-1,"description":"protein tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:9611]"}, {"versioned_ensembl_gene_id":"ENSG00000284490.1","gene_symbol":"AC011471.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6199405,"end":6205121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274444.1","gene_symbol":"AC078909.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37109587,"end":37109984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058453.16","gene_symbol":"CROCC","gene_name":"ciliary rootlet coiled-coil, rootletin [Source:HGNC Symbol;Acc:HGNC:21299]","synonyms":"rootletin,ROLT","biotype":"protein_coding","ncbi_id":"9696","summary":null,"start":16740273,"end":16972979,"strand":1,"description":"ciliary rootlet coiled-coil, rootletin [Source:HGNC Symbol;Acc:HGNC:21299]"}, {"versioned_ensembl_gene_id":"ENSG00000257279.1","gene_symbol":"AC127164.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116977442,"end":116987337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163155.11","gene_symbol":"LYSMD1","gene_name":"LysM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32070]","synonyms":"SB145,RP11-68I18.5,MGC35223","biotype":"protein_coding","ncbi_id":"388695","summary":null,"start":151159748,"end":151165948,"strand":-1,"description":"LysM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32070]"}, {"versioned_ensembl_gene_id":"ENSG00000239653.1","gene_symbol":"PSMD6-AS2","gene_name":"PSMD6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507062","summary":null,"start":64004022,"end":64012148,"strand":1,"description":"PSMD6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44125]"}, {"versioned_ensembl_gene_id":"ENSG00000239569.3","gene_symbol":"KMT2E-AS1","gene_name":"KMT2E antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40845]","synonyms":"LOC100216545","biotype":"antisense_RNA","ncbi_id":"100216545","summary":null,"start":105013425,"end":105014321,"strand":-1,"description":"KMT2E antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40845]"}, {"versioned_ensembl_gene_id":"ENSG00000282278.1","gene_symbol":"AC058822.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53377839,"end":54295272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182450.12","gene_symbol":"KCNK4","gene_name":"potassium two pore domain channel subfamily K member 4 [Source:HGNC Symbol;Acc:HGNC:6279]","synonyms":"TRAAK,K2p4.1","biotype":"protein_coding","ncbi_id":"50801","summary":"This gene encodes a member of the TWIK-related arachidonic acid-stimulated two pore potassium channel subfamily. The encoded protein homodimerizes and functions as an outwardly rectifying channel. This channel is regulated by polyunsaturated fatty acids, temperature and mechanical deformation of the lipid membrane. This protein is expressed primarily in neural tissues and may be involved in regulating the noxious input threshold in dorsal root ganglia neurons. Alternate splicing results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream testis expressed 40 (TEX40) gene, as represented in GeneID: 106780802. [provided by RefSeq, Nov 2015]","start":64291302,"end":64300031,"strand":1,"description":"potassium two pore domain channel subfamily K member 4 [Source:HGNC Symbol;Acc:HGNC:6279]"}, {"versioned_ensembl_gene_id":"ENSG00000243410.1","gene_symbol":"PSMD6-AS1","gene_name":"PSMD6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40480]","synonyms":"lnc00462717,ENST00000462717","biotype":"antisense_RNA","ncbi_id":"109729140","summary":null,"start":64011964,"end":64016246,"strand":1,"description":"PSMD6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40480]"}, {"versioned_ensembl_gene_id":"ENSG00000177628.15","gene_symbol":"GBA","gene_name":"glucosylceramidase beta [Source:HGNC Symbol;Acc:HGNC:4177]","synonyms":"GLUC,GBA1","biotype":"protein_coding","ncbi_id":"2629","summary":"This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010]","start":155234452,"end":155244699,"strand":-1,"description":"glucosylceramidase beta [Source:HGNC Symbol;Acc:HGNC:4177]"}, {"versioned_ensembl_gene_id":"ENSG00000251049.2","gene_symbol":"AC107396.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57595940,"end":57605872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233223.2","gene_symbol":"AC016876.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7581964,"end":7584072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261277.2","gene_symbol":"OR4H6P","gene_name":"olfactory receptor family 4 subfamily H member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:8312]","synonyms":"OR15-71,OR4H4,OR15-69,OR4H3P,OR14-58,OR4H3,OR4H2P,OR4H2,OR5-84,OR4H1P,OR5-39,OR4H11P,OR4H9P,OR4H11,OR4H9,OR4H10P,OR4H8P,OR4H10,OR4H8,OR4-119,OR4H7P,OR4-115,OR4H7,OR4-114,OR4H6,OR15-82,OR4H5P,OR15-81,OR4H5,OR15-80,OR4H4P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26322","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22056709,"end":22057949,"strand":1,"description":"olfactory receptor family 4 subfamily H member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:8312]"}, {"versioned_ensembl_gene_id":"ENSG00000237853.6","gene_symbol":"NFIA-AS1","gene_name":"NFIA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40402]","synonyms":"RP5-833A20.1","biotype":"processed_transcript","ncbi_id":"645030","summary":null,"start":61248945,"end":61253510,"strand":-1,"description":"NFIA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40402]"}, {"versioned_ensembl_gene_id":"ENSG00000185798.7","gene_symbol":"WDR53","gene_name":"WD repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:28786]","synonyms":"MGC64882,MGC12928","biotype":"protein_coding","ncbi_id":"348793","summary":"This gene encodes a protein containing WD domains. The function of this gene is unknown. [provided by RefSeq, Jul 2008]","start":196554177,"end":196568674,"strand":-1,"description":"WD repeat domain 53 [Source:HGNC Symbol;Acc:HGNC:28786]"}, {"versioned_ensembl_gene_id":"ENSG00000258786.1","gene_symbol":"AC183089.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21980321,"end":21981209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282143.1","gene_symbol":"AL137798.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16656879,"end":16667524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233816.3","gene_symbol":"IFNA13","gene_name":"interferon alpha 13 [Source:HGNC Symbol;Acc:HGNC:5419]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3447","summary":null,"start":21367424,"end":21368962,"strand":-1,"description":"interferon alpha 13 [Source:HGNC Symbol;Acc:HGNC:5419]"}, {"versioned_ensembl_gene_id":"ENSG00000135519.6","gene_symbol":"KCNH3","gene_name":"potassium voltage-gated channel subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:6252]","synonyms":"Kv12.2,elk2,BEC1","biotype":"protein_coding","ncbi_id":"23416","summary":"The protein encoded by this gene is a voltage-gated potassium channel alpha subunit predominantly expressed in the forebrain. Studies in mice have found that cognitive function increases when this gene is knocked out. In humans, the encoded protein has been shown to be capable of binding glycoprotein 120 of the human immunodeficiency virus type 1 (HIV-1) envelope. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":49539157,"end":49558308,"strand":1,"description":"potassium voltage-gated channel subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:6252]"}, {"versioned_ensembl_gene_id":"ENSG00000278769.1","gene_symbol":"AC090510.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42724102,"end":42724922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223757.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"NG37,G7c,C6orf27","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31841886,"end":31853590,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000258585.2","gene_symbol":"ZNF519P3","gene_name":"zinc finger protein 519 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50787]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288042","summary":null,"start":21911559,"end":21912590,"strand":-1,"description":"zinc finger protein 519 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50787]"}, {"versioned_ensembl_gene_id":"ENSG00000156928.4","gene_symbol":"MALSU1","gene_name":"mitochondrial assembly of ribosomal large subunit 1 [Source:HGNC Symbol;Acc:HGNC:21721]","synonyms":"mtRsfA,C7orf30","biotype":"protein_coding","ncbi_id":"115416","summary":null,"start":23298739,"end":23311729,"strand":1,"description":"mitochondrial assembly of ribosomal large subunit 1 [Source:HGNC Symbol;Acc:HGNC:21721]"}, {"versioned_ensembl_gene_id":"ENSG00000279605.1","gene_symbol":"AC067930.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":143578358,"end":143583304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151348.13","gene_symbol":"EXT2","gene_name":"exostosin glycosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:3513]","synonyms":"SOTV","biotype":"protein_coding","ncbi_id":"2132","summary":"This gene encodes one of two glycosyltransferases involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type II form of multiple exostoses. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]","start":44095549,"end":44245429,"strand":1,"description":"exostosin glycosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:3513]"}, {"versioned_ensembl_gene_id":"ENSG00000182670.13","gene_symbol":"TTC3","gene_name":"tetratricopeptide repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12393]","synonyms":"RNF105,DCRR1,TPRDIII,TPRDII,TPRDI,TPRD","biotype":"protein_coding","ncbi_id":"7267","summary":null,"start":37073226,"end":37203112,"strand":1,"description":"tetratricopeptide repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:12393]"}, {"versioned_ensembl_gene_id":"ENSG00000226869.6","gene_symbol":"LHFPL3-AS1","gene_name":"LHFPL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40341]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"645591","summary":null,"start":104738597,"end":104804107,"strand":-1,"description":"LHFPL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40341]"}, {"versioned_ensembl_gene_id":"ENSG00000243979.2","gene_symbol":"AC087752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94891239,"end":94892107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259656.1","gene_symbol":"AC013452.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49101791,"end":49103264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205883.2","gene_symbol":"DEFB135","gene_name":"defensin beta 135 [Source:HGNC Symbol;Acc:HGNC:32400]","synonyms":null,"biotype":"protein_coding","ncbi_id":"613209","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 8p23. [provided by RefSeq, Nov 2014]","start":11982321,"end":11984590,"strand":1,"description":"defensin beta 135 [Source:HGNC Symbol;Acc:HGNC:32400]"}, {"versioned_ensembl_gene_id":"ENSG00000263627.1","gene_symbol":"PPP4R1-AS1","gene_name":"PPP4R1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51112]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927323","summary":null,"start":9615264,"end":9619363,"strand":1,"description":"PPP4R1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51112]"}, {"versioned_ensembl_gene_id":"ENSG00000236581.8","gene_symbol":"STARD13-AS","gene_name":"STARD13 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40873]","synonyms":"STARD13-AS2","biotype":"processed_transcript","ncbi_id":"100874241","summary":null,"start":33180401,"end":33281584,"strand":1,"description":"STARD13 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40873]"}, {"versioned_ensembl_gene_id":"ENSG00000189134.3","gene_symbol":"NKAPL","gene_name":"NFKB activating protein like [Source:HGNC Symbol;Acc:HGNC:21584]","synonyms":"C6orf194,bA424I5.1","biotype":"protein_coding","ncbi_id":"222698","summary":null,"start":28259320,"end":28260958,"strand":1,"description":"NFKB activating protein like [Source:HGNC Symbol;Acc:HGNC:21584]"}, {"versioned_ensembl_gene_id":"ENSG00000261291.1","gene_symbol":"AC007906.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53168522,"end":53169450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279589.1","gene_symbol":"AC079416.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53310797,"end":53311989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261719.1","gene_symbol":"AC137761.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32811029,"end":32811251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237568.1","gene_symbol":"AC099063.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89260582,"end":89269754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260158.1","gene_symbol":"AC137761.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32809556,"end":32824645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282836.1","gene_symbol":"AC068544.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":196638422,"end":196639497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257636.6","gene_symbol":"G2E3-AS1","gene_name":"G2E3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53463]","synonyms":"CAT1647","biotype":"antisense_RNA","ncbi_id":"105370431","summary":null,"start":30437992,"end":30573629,"strand":-1,"description":"G2E3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53463]"}, {"versioned_ensembl_gene_id":"ENSG00000271732.1","gene_symbol":"AL137798.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16617391,"end":16617729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203877.8","gene_symbol":"RIPPLY2","gene_name":"ripply transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:21390]","synonyms":"dJ237I15.1,C6orf159","biotype":"protein_coding","ncbi_id":"134701","summary":"This gene encodes a nuclear protein that belongs to a novel family of proteins required for vertebrate somitogenesis. Members of this family have a tetrapeptide WRPW motif that is required for interaction with the transcriptional repressor Groucho and a carboxy-terminal Ripply homology domain/Bowline-DSCR-Ledgerline conserved region required for transcriptional repression. Null mutant mice die soon after birth and display defects in axial skeleton segmentation due to defective somitogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":83853266,"end":83857515,"strand":1,"description":"ripply transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:21390]"}, {"versioned_ensembl_gene_id":"ENSG00000262990.1","gene_symbol":"AC004706.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6749685,"end":6749978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244283.1","gene_symbol":"RPL23AP73","gene_name":"ribosomal protein L23a pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:36443]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271625","summary":null,"start":6749718,"end":6750188,"strand":1,"description":"ribosomal protein L23a pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:36443]"}, {"versioned_ensembl_gene_id":"ENSG00000033011.11","gene_symbol":"ALG1","gene_name":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:18294]","synonyms":"Mat-1,HMT-1,HMAT1,CDG1K","biotype":"protein_coding","ncbi_id":"56052","summary":"The enzyme encoded by this gene catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. This gene is mutated in congenital disorder of glycosylation type Ik. [provided by RefSeq, Dec 2008]","start":5033960,"end":5087379,"strand":1,"description":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:18294]"}, {"versioned_ensembl_gene_id":"ENSG00000065970.8","gene_symbol":"FOXJ2","gene_name":"forkhead box J2 [Source:HGNC Symbol;Acc:HGNC:24818]","synonyms":"FHX","biotype":"protein_coding","ncbi_id":"55810","summary":null,"start":8032703,"end":8055503,"strand":1,"description":"forkhead box J2 [Source:HGNC Symbol;Acc:HGNC:24818]"}, {"versioned_ensembl_gene_id":"ENSG00000281898.1","gene_symbol":"AC217778.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45396950,"end":45397495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224821.5","gene_symbol":"COL4A2-AS2","gene_name":"COL4A2 antisense 2 [Source:HGNC Symbol;Acc:HGNC:39849]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129836","summary":null,"start":110456396,"end":110463287,"strand":-1,"description":"COL4A2 antisense 2 [Source:HGNC Symbol;Acc:HGNC:39849]"}, {"versioned_ensembl_gene_id":"ENSG00000099795.6","gene_symbol":"NDUFB7","gene_name":"NADH:ubiquinone oxidoreductase subunit B7 [Source:HGNC Symbol;Acc:HGNC:7702]","synonyms":"MGC2480,CI-B18,B18","biotype":"protein_coding","ncbi_id":"4713","summary":"The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [provided by RefSeq, Jul 2008]","start":14566078,"end":14572062,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B7 [Source:HGNC Symbol;Acc:HGNC:7702]"}, {"versioned_ensembl_gene_id":"ENSG00000138182.14","gene_symbol":"KIF20B","gene_name":"kinesin family member 20B [Source:HGNC Symbol;Acc:HGNC:7212]","synonyms":"MPP1,MPHOSPH1,KRMP1,CT90","biotype":"protein_coding","ncbi_id":"9585","summary":null,"start":89701610,"end":89774939,"strand":1,"description":"kinesin family member 20B [Source:HGNC Symbol;Acc:HGNC:7212]"}, {"versioned_ensembl_gene_id":"ENSG00000176890.15","gene_symbol":"TYMS","gene_name":"thymidylate synthetase [Source:HGNC Symbol;Acc:HGNC:12441]","synonyms":"Tsase,TS,TMS,HsT422","biotype":"protein_coding","ncbi_id":"7298","summary":"Thymidylate synthase catalyzes the methylation of deoxyuridylate to deoxythymidylate using, 10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs. Expression of this gene and that of a naturally occurring antisense transcript, mitochondrial enolase superfamily member 1 (GeneID:55556), vary inversely when cell-growth progresses from late-log to plateau phase. Polymorphisms in this gene may be associated with etiology of neoplasia, including breast cancer, and response to chemotherapy. [provided by RefSeq, Aug 2017]","start":657604,"end":673578,"strand":1,"description":"thymidylate synthetase [Source:HGNC Symbol;Acc:HGNC:12441]"}, {"versioned_ensembl_gene_id":"ENSG00000224619.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ31598,FLJ25550,Em:AB014087.1","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30280729,"end":30317069,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000283286.1","gene_symbol":"AC093277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40415137,"end":40431491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267116.1","gene_symbol":"AP005264.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12192203,"end":12192934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263727.1","gene_symbol":"AP001178.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":653985,"end":657259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230208.1","gene_symbol":"IFNNP1","gene_name":"interferon nu 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:32009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654783","summary":null,"start":21058771,"end":21059323,"strand":-1,"description":"interferon nu 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:32009]"}, {"versioned_ensembl_gene_id":"ENSG00000260622.1","gene_symbol":"AC073476.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231810348,"end":231810844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277251.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"cl-43,CD158B1,nkat6,CD158k","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754680,"end":54769221,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000268629.6","gene_symbol":"TEX13A","gene_name":"testis expressed 13A [Source:HGNC Symbol;Acc:HGNC:11735]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56157","summary":"This gene is similar to a mouse gene that is expressed in the testis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":105218929,"end":105220674,"strand":-1,"description":"testis expressed 13A [Source:HGNC Symbol;Acc:HGNC:11735]"}, {"versioned_ensembl_gene_id":"ENSG00000247796.2","gene_symbol":"AC008966.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53109842,"end":53115126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261122.6","gene_symbol":"LINC02167","gene_name":"long intergenic non-protein coding RNA 2167 [Source:HGNC Symbol;Acc:HGNC:53028]","synonyms":"FLJ26245","biotype":"lincRNA","ncbi_id":"400533","summary":null,"start":35743268,"end":35756515,"strand":1,"description":"long intergenic non-protein coding RNA 2167 [Source:HGNC Symbol;Acc:HGNC:53028]"}, {"versioned_ensembl_gene_id":"ENSG00000239919.1","gene_symbol":"SNRPGP3","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39322]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874407","summary":null,"start":129477875,"end":129478101,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39322]"}, {"versioned_ensembl_gene_id":"ENSG00000233358.2","gene_symbol":"AL035401.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22744395,"end":23031780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228772.2","gene_symbol":"AL033539.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22589137,"end":22593833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249858.2","gene_symbol":"SNX5P1","gene_name":"sorting nexin 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41512]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131940","summary":null,"start":76344550,"end":76345590,"strand":1,"description":"sorting nexin 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41512]"}, {"versioned_ensembl_gene_id":"ENSG00000133121.20","gene_symbol":"STARD13","gene_name":"StAR related lipid transfer domain containing 13 [Source:HGNC Symbol;Acc:HGNC:19164]","synonyms":"LINC00464,GT650,DLC2,ARHGAP37","biotype":"protein_coding","ncbi_id":"90627","summary":"This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":33103135,"end":33350630,"strand":-1,"description":"StAR related lipid transfer domain containing 13 [Source:HGNC Symbol;Acc:HGNC:19164]"}, {"versioned_ensembl_gene_id":"ENSG00000122033.14","gene_symbol":"MTIF3","gene_name":"mitochondrial translational initiation factor 3 [Source:HGNC Symbol;Acc:HGNC:29788]","synonyms":"IF3(mt),IF-3mt","biotype":"protein_coding","ncbi_id":"219402","summary":"This gene encodes a translation initiation factor that is involved in mitochondrial protein synthesis. Polymorphism in this gene is associated with the onset of Parkinson's disease. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 5. [provided by RefSeq, Oct 2009]","start":27435643,"end":27450591,"strand":-1,"description":"mitochondrial translational initiation factor 3 [Source:HGNC Symbol;Acc:HGNC:29788]"}, {"versioned_ensembl_gene_id":"ENSG00000254900.1","gene_symbol":"AC091053.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8679089,"end":8680913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255144.1","gene_symbol":"AC025857.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11895850,"end":11896870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270558.1","gene_symbol":"AC025449.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37286449,"end":37286977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258754.7","gene_symbol":"LINC01579","gene_name":"long intergenic non-protein coding RNA 1579 [Source:HGNC Symbol;Acc:HGNC:27519]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283682","summary":null,"start":93718542,"end":94070820,"strand":-1,"description":"long intergenic non-protein coding RNA 1579 [Source:HGNC Symbol;Acc:HGNC:27519]"}, {"versioned_ensembl_gene_id":"ENSG00000257193.1","gene_symbol":"LINC02385","gene_name":"long intergenic non-protein coding RNA 2385 [Source:HGNC Symbol;Acc:HGNC:53309]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369948","summary":null,"start":104170395,"end":104177659,"strand":1,"description":"long intergenic non-protein coding RNA 2385 [Source:HGNC Symbol;Acc:HGNC:53309]"}, {"versioned_ensembl_gene_id":"ENSG00000270934.1","gene_symbol":"AL512430.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110598093,"end":110598705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102218.5","gene_symbol":"RP2","gene_name":"RP2, ARL3 GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:10274]","synonyms":"TBCCD2,NME10,NM23-H10","biotype":"protein_coding","ncbi_id":"6102","summary":"The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death [provided by RefSeq, Jul 2008]","start":46836940,"end":46882358,"strand":1,"description":"RP2, ARL3 GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:10274]"}, {"versioned_ensembl_gene_id":"ENSG00000187605.15","gene_symbol":"TET3","gene_name":"tet methylcytosine dioxygenase 3 [Source:HGNC Symbol;Acc:HGNC:28313]","synonyms":"MGC22014,hCG_40738","biotype":"protein_coding","ncbi_id":"200424","summary":"Members of the ten-eleven translocation (TET) gene family, including TET3, play a role in the DNA methylation process (Langemeijer et al., 2009 [PubMed 19923888]).[supplied by OMIM, Nov 2010]","start":73986404,"end":74108176,"strand":1,"description":"tet methylcytosine dioxygenase 3 [Source:HGNC Symbol;Acc:HGNC:28313]"}, {"versioned_ensembl_gene_id":"ENSG00000240996.1","gene_symbol":"AL157400.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89694295,"end":89697928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253891.1","gene_symbol":"AC023202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24169957,"end":24177080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125351.11","gene_symbol":"UPF3B","gene_name":"UPF3B, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:20439]","synonyms":"HUPF3B,UPF3X,UPF3BP3,UPF3BP2,UPF3BP1,RENT3B,MRX62","biotype":"protein_coding","ncbi_id":"65109","summary":"This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. The encoded protein is one of two functional homologs to yeast Upf3p. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein binds to the mRNA and remains bound after nuclear export, acting as a nucleocytoplasmic shuttling protein. It forms with Y14 a complex that binds specifically 20 nt upstream of exon-exon junctions. This gene is located on the long arm of chromosome X. Two splice variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":119805311,"end":119852998,"strand":-1,"description":"UPF3B, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:20439]"}, {"versioned_ensembl_gene_id":"ENSG00000235100.3","gene_symbol":"AL157400.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89667181,"end":89699671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081154.11","gene_symbol":"PCNP","gene_name":"PEST proteolytic signal containing nuclear protein [Source:HGNC Symbol;Acc:HGNC:30023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57092","summary":null,"start":101574095,"end":101594437,"strand":1,"description":"PEST proteolytic signal containing nuclear protein [Source:HGNC Symbol;Acc:HGNC:30023]"}, {"versioned_ensembl_gene_id":"ENSG00000270479.1","gene_symbol":"BNIP3P37","gene_name":"BCL2 interacting protein 3 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:49717]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480285","summary":null,"start":23123188,"end":23124088,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:49717]"}, {"versioned_ensembl_gene_id":"ENSG00000267886.1","gene_symbol":"AC074135.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23075201,"end":23100361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279032.1","gene_symbol":"AL079305.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30370108,"end":30373115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268812.3","gene_symbol":"AC004264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30246205,"end":30246998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278952.1","gene_symbol":"AP003068.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":65118310,"end":65119111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128342.4","gene_symbol":"LIF","gene_name":"LIF, interleukin 6 family cytokine [Source:HGNC Symbol;Acc:HGNC:6596]","synonyms":"HILDA,DIA,CDF","biotype":"protein_coding","ncbi_id":"3976","summary":"The protein encoded by this gene is a pleiotropic cytokine with roles in several different systems. It is involved in the induction of hematopoietic differentiation in normal and myeloid leukemia cells, induction of neuronal cell differentiation, regulator of mesenchymal to epithelial conversion during kidney development, and may also have a role in immune tolerance at the maternal-fetal interface. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":30240447,"end":30246851,"strand":-1,"description":"LIF, interleukin 6 family cytokine [Source:HGNC Symbol;Acc:HGNC:6596]"}, {"versioned_ensembl_gene_id":"ENSG00000115226.9","gene_symbol":"FNDC4","gene_name":"fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:20239]","synonyms":"FRCP1,FLJ22362","biotype":"protein_coding","ncbi_id":"64838","summary":null,"start":27491883,"end":27495245,"strand":-1,"description":"fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:HGNC:20239]"}, {"versioned_ensembl_gene_id":"ENSG00000253528.2","gene_symbol":"AC087752.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94974573,"end":94974853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156170.12","gene_symbol":"NDUFAF6","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 6 [Source:HGNC Symbol;Acc:HGNC:28625]","synonyms":"MGC40214,C8orf38","biotype":"protein_coding","ncbi_id":"137682","summary":"This gene encodes a protein that localizes to mitochondria and contains a predicted phytoene synthase domain. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis. Mutations in this gene are associated with complex I enzymatic deficiency. [provided by RefSeq, Nov 2011]","start":94895767,"end":95116455,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 6 [Source:HGNC Symbol;Acc:HGNC:28625]"}, {"versioned_ensembl_gene_id":"ENSG00000163913.11","gene_symbol":"IFT122","gene_name":"intraflagellar transport 122 [Source:HGNC Symbol;Acc:HGNC:13556]","synonyms":"WDR140,WDR10p,WDR10,SPG","biotype":"protein_coding","ncbi_id":"55764","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":129440036,"end":129520507,"strand":1,"description":"intraflagellar transport 122 [Source:HGNC Symbol;Acc:HGNC:13556]"}, {"versioned_ensembl_gene_id":"ENSG00000240833.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30224388,"end":30316053,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000201392.1","gene_symbol":"RNU6-1078P","gene_name":"RNA, U6 small nuclear 1078, pseudogene [Source:HGNC Symbol;Acc:HGNC:48041]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481519","summary":null,"start":71965972,"end":71966074,"strand":-1,"description":"RNA, U6 small nuclear 1078, pseudogene [Source:HGNC Symbol;Acc:HGNC:48041]"}, {"versioned_ensembl_gene_id":"ENSG00000199455.1","gene_symbol":"RNA5SP191","gene_name":"RNA, 5S ribosomal pseudogene 191 [Source:HGNC Symbol;Acc:HGNC:43091]","synonyms":"RN5S191","biotype":"rRNA","ncbi_id":"100873453","summary":null,"start":130114409,"end":130114510,"strand":1,"description":"RNA, 5S ribosomal pseudogene 191 [Source:HGNC Symbol;Acc:HGNC:43091]"}, {"versioned_ensembl_gene_id":"ENSG00000200903.1","gene_symbol":"RNU1-42P","gene_name":"RNA, U1 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:48384]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481609","summary":null,"start":48949361,"end":48949520,"strand":-1,"description":"RNA, U1 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:48384]"}, {"versioned_ensembl_gene_id":"ENSG00000275167.1","gene_symbol":"MIR6815","gene_name":"microRNA 6815 [Source:HGNC Symbol;Acc:HGNC:50225]","synonyms":"hsa-mir-6815","biotype":"miRNA","ncbi_id":"102465489","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45478266,"end":45478326,"strand":1,"description":"microRNA 6815 [Source:HGNC Symbol;Acc:HGNC:50225]"}, {"versioned_ensembl_gene_id":"ENSG00000212332.1","gene_symbol":"RNU6-780P","gene_name":"RNA, U6 small nuclear 780, pseudogene [Source:HGNC Symbol;Acc:HGNC:47743]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481427","summary":null,"start":86488446,"end":86488549,"strand":1,"description":"RNA, U6 small nuclear 780, pseudogene [Source:HGNC Symbol;Acc:HGNC:47743]"}, {"versioned_ensembl_gene_id":"ENSG00000244318.3","gene_symbol":"RN7SL252P","gene_name":"RNA, 7SL, cytoplasmic 252, pseudogene [Source:HGNC Symbol;Acc:HGNC:46268]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481832","summary":null,"start":96940068,"end":96940364,"strand":-1,"description":"RNA, 7SL, cytoplasmic 252, pseudogene [Source:HGNC Symbol;Acc:HGNC:46268]"}, {"versioned_ensembl_gene_id":"ENSG00000266665.1","gene_symbol":"MIR4739","gene_name":"microRNA 4739 [Source:HGNC Symbol;Acc:HGNC:41801]","synonyms":"hsa-mir-4739","biotype":"miRNA","ncbi_id":"100616170","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79707176,"end":79707249,"strand":-1,"description":"microRNA 4739 [Source:HGNC Symbol;Acc:HGNC:41801]"}, {"versioned_ensembl_gene_id":"ENSG00000242330.3","gene_symbol":"RN7SL683P","gene_name":"RNA, 7SL, cytoplasmic 683, pseudogene [Source:HGNC Symbol;Acc:HGNC:46699]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481109","summary":null,"start":71448689,"end":71448958,"strand":1,"description":"RNA, 7SL, cytoplasmic 683, pseudogene [Source:HGNC Symbol;Acc:HGNC:46699]"}, {"versioned_ensembl_gene_id":"ENSG00000199512.1","gene_symbol":"RNU6-212P","gene_name":"RNA, U6 small nuclear 212, pseudogene [Source:HGNC Symbol;Acc:HGNC:47175]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481243","summary":null,"start":59341314,"end":59341417,"strand":-1,"description":"RNA, U6 small nuclear 212, pseudogene [Source:HGNC Symbol;Acc:HGNC:47175]"}, {"versioned_ensembl_gene_id":"ENSG00000201923.1","gene_symbol":"RNA5SP485","gene_name":"RNA, 5S ribosomal pseudogene 485 [Source:HGNC Symbol;Acc:HGNC:43385]","synonyms":"RN5S485","biotype":"rRNA","ncbi_id":"100873727","summary":null,"start":45559758,"end":45559876,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 485 [Source:HGNC Symbol;Acc:HGNC:43385]"}, {"versioned_ensembl_gene_id":"ENSG00000202395.1","gene_symbol":"RN7SKP1","gene_name":"RNA, 7SK small nuclear pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42619]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873845","summary":null,"start":37166352,"end":37166658,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42619]"}, {"versioned_ensembl_gene_id":"ENSG00000251781.1","gene_symbol":"RNA5SP356","gene_name":"RNA, 5S ribosomal pseudogene 356 [Source:HGNC Symbol;Acc:HGNC:43256]","synonyms":"RN5S356","biotype":"rRNA","ncbi_id":"100873615","summary":null,"start":30306431,"end":30306524,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 356 [Source:HGNC Symbol;Acc:HGNC:43256]"}, {"versioned_ensembl_gene_id":"ENSG00000266075.2","gene_symbol":"RN7SL574P","gene_name":"RNA, 7SL, cytoplasmic 574, pseudogene [Source:HGNC Symbol;Acc:HGNC:46590]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481079","summary":null,"start":3782815,"end":3783111,"strand":1,"description":"RNA, 7SL, cytoplasmic 574, pseudogene [Source:HGNC Symbol;Acc:HGNC:46590]"}, {"versioned_ensembl_gene_id":"ENSG00000199516.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129954693,"end":129954794,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241243.3","gene_symbol":"RN7SL629P","gene_name":"RNA, 7SL, cytoplasmic 629, pseudogene [Source:HGNC Symbol;Acc:HGNC:46645]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479452","summary":null,"start":87294189,"end":87294473,"strand":-1,"description":"RNA, 7SL, cytoplasmic 629, pseudogene [Source:HGNC Symbol;Acc:HGNC:46645]"}, {"versioned_ensembl_gene_id":"ENSG00000212241.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":115139030,"end":115139123,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252174.1","gene_symbol":"RNU7-18P","gene_name":"RNA, U7 small nuclear 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:34114]","synonyms":"U7.18,RNU7-142P","biotype":"snRNA","ncbi_id":"100147766","summary":null,"start":196072819,"end":196072880,"strand":1,"description":"RNA, U7 small nuclear 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:34114]"}, {"versioned_ensembl_gene_id":"ENSG00000274452.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43290291,"end":43290481,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000242547.3","gene_symbol":"RN7SL169P","gene_name":"RNA, 7SL, cytoplasmic 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:46185]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480372","summary":null,"start":64539504,"end":64539792,"strand":1,"description":"RNA, 7SL, cytoplasmic 169, pseudogene [Source:HGNC Symbol;Acc:HGNC:46185]"}, {"versioned_ensembl_gene_id":"ENSG00000206849.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":31928303,"end":31928434,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000212359.1","gene_symbol":"RNU6-550P","gene_name":"RNA, U6 small nuclear 550, pseudogene [Source:HGNC Symbol;Acc:HGNC:47513]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481355","summary":null,"start":120810469,"end":120810569,"strand":1,"description":"RNA, U6 small nuclear 550, pseudogene [Source:HGNC Symbol;Acc:HGNC:47513]"}, {"versioned_ensembl_gene_id":"ENSG00000206597.1","gene_symbol":"SNORA57","gene_name":"small nucleolar RNA, H/ACA box 57 [Source:HGNC Symbol;Acc:HGNC:32651]","synonyms":"U99","biotype":"snoRNA","ncbi_id":"692158","summary":null,"start":62665422,"end":62665570,"strand":1,"description":"small nucleolar RNA, H/ACA box 57 [Source:HGNC Symbol;Acc:HGNC:32651]"}, {"versioned_ensembl_gene_id":"ENSG00000275330.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000206901.1","gene_symbol":"SNORA72","gene_name":"Small nucleolar RNA SNORA72 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[provided by RefSeq, Sep 2009]","start":46018932,"end":46019049,"strand":1,"description":"microRNA 769 [Source:HGNC Symbol;Acc:HGNC:33138]"}, {"versioned_ensembl_gene_id":"ENSG00000200161.1","gene_symbol":"RN7SKP145","gene_name":"RNA, 7SK small nuclear pseudogene 145 [Source:HGNC Symbol;Acc:HGNC:45869]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480878","summary":null,"start":149116178,"end":149116480,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 145 [Source:HGNC Symbol;Acc:HGNC:45869]"}, {"versioned_ensembl_gene_id":"ENSG00000275724.1","gene_symbol":"AC012314.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200206.1","gene_symbol":"SNORD74","gene_name":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]","synonyms":null,"biotype":"snoRNA","ncbi_id":"619498","summary":null,"start":86173198,"end":86173270,"strand":-1,"description":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]"}, {"versioned_ensembl_gene_id":"ENSG00000265376.1","gene_symbol":"MIR466","gene_name":"microRNA 466 [Source:HGNC Symbol;Acc:HGNC:38359]","synonyms":"hsa-mir-466","biotype":"miRNA","ncbi_id":"100423038","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31161704,"end":31161787,"strand":-1,"description":"microRNA 466 [Source:HGNC Symbol;Acc:HGNC:38359]"}, {"versioned_ensembl_gene_id":"ENSG00000252858.1","gene_symbol":"RNU6-1271P","gene_name":"RNA, U6 small nuclear 1271, pseudogene [Source:HGNC Symbol;Acc:HGNC:48234]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480120","summary":null,"start":76139567,"end":76139671,"strand":1,"description":"RNA, U6 small nuclear 1271, pseudogene [Source:HGNC Symbol;Acc:HGNC:48234]"}, {"versioned_ensembl_gene_id":"ENSG00000274969.1","gene_symbol":"MIR6771","gene_name":"microRNA 6771 [Source:HGNC Symbol;Acc:HGNC:50212]","synonyms":"hsa-mir-6771","biotype":"miRNA","ncbi_id":"102465462","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50292616,"end":50292675,"strand":1,"description":"microRNA 6771 [Source:HGNC Symbol;Acc:HGNC:50212]"}, {"versioned_ensembl_gene_id":"ENSG00000264226.1","gene_symbol":"MIR3168","gene_name":"microRNA 3168 [Source:HGNC Symbol;Acc:HGNC:38249]","synonyms":"hsa-mir-3168","biotype":"miRNA","ncbi_id":"100422878","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41101019,"end":41101100,"strand":-1,"description":"microRNA 3168 [Source:HGNC Symbol;Acc:HGNC:38249]"}, {"versioned_ensembl_gene_id":"ENSG00000212184.1","gene_symbol":"RNU6-440P","gene_name":"RNA, U6 small nuclear 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:47403]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481895","summary":null,"start":201927439,"end":201927543,"strand":1,"description":"RNA, U6 small nuclear 440, pseudogene [Source:HGNC Symbol;Acc:HGNC:47403]"}, {"versioned_ensembl_gene_id":"ENSG00000222924.1","gene_symbol":"RNU6-1148P","gene_name":"RNA, U6 small nuclear 1148, pseudogene [Source:HGNC Symbol;Acc:HGNC:48111]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480642","summary":null,"start":138069355,"end":138069458,"strand":-1,"description":"RNA, U6 small nuclear 1148, pseudogene [Source:HGNC Symbol;Acc:HGNC:48111]"}, {"versioned_ensembl_gene_id":"ENSG00000252020.1","gene_symbol":"SCARNA17","gene_name":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]","synonyms":"mgU12-22/U4-8,U91","biotype":"scaRNA","ncbi_id":"677769","summary":null,"start":21389796,"end":21389938,"strand":-1,"description":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]"}, {"versioned_ensembl_gene_id":"ENSG00000240977.3","gene_symbol":"RN7SL283P","gene_name":"RNA, 7SL, cytoplasmic 283, pseudogene [Source:HGNC Symbol;Acc:HGNC:46299]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479325","summary":null,"start":139982684,"end":139982986,"strand":1,"description":"RNA, 7SL, cytoplasmic 283, pseudogene [Source:HGNC Symbol;Acc:HGNC:46299]"}, {"versioned_ensembl_gene_id":"ENSG00000199546.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49270132,"end":49270239,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263882.2","gene_symbol":"RN7SL774P","gene_name":"RNA, 7SL, cytoplasmic 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:46790]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481761","summary":null,"start":4364164,"end":4364453,"strand":-1,"description":"RNA, 7SL, cytoplasmic 774, pseudogene [Source:HGNC Symbol;Acc:HGNC:46790]"}, {"versioned_ensembl_gene_id":"ENSG00000252072.1","gene_symbol":"RNA5SP320","gene_name":"RNA, 5S ribosomal pseudogene 320 [Source:HGNC Symbol;Acc:HGNC:43220]","synonyms":"RN5S320","biotype":"rRNA","ncbi_id":"100873586","summary":null,"start":73706490,"end":73706613,"strand":1,"description":"RNA, 5S ribosomal pseudogene 320 [Source:HGNC Symbol;Acc:HGNC:43220]"}, {"versioned_ensembl_gene_id":"ENSG00000222404.1","gene_symbol":"RN7SKP281","gene_name":"RNA, 7SK small nuclear pseudogene 281 [Source:HGNC Symbol;Acc:HGNC:46005]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480369","summary":null,"start":157298807,"end":157299158,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 281 [Source:HGNC Symbol;Acc:HGNC:46005]"}, {"versioned_ensembl_gene_id":"ENSG00000212443.1","gene_symbol":"SNORA53","gene_name":"small nucleolar RNA, H/ACA box 53 [Source:HGNC Symbol;Acc:HGNC:32646]","synonyms":"ACA53","biotype":"snoRNA","ncbi_id":"677832","summary":null,"start":98599635,"end":98599883,"strand":1,"description":"small nucleolar RNA, H/ACA box 53 [Source:HGNC Symbol;Acc:HGNC:32646]"}, {"versioned_ensembl_gene_id":"ENSG00000275110.1","gene_symbol":"MIR6087","gene_name":"microRNA 6087 [Source:HGNC Symbol;Acc:HGNC:50045]","synonyms":"hsa-mir-6087","biotype":"miRNA","ncbi_id":"102464835","summary":"This record was withdrawn by miRBase.","start":109054542,"end":109054590,"strand":1,"description":"microRNA 6087 [Source:HGNC Symbol;Acc:HGNC:50045]"}, {"versioned_ensembl_gene_id":"ENSG00000275519.1","gene_symbol":"MIR6804","gene_name":"microRNA 6804 [Source:HGNC Symbol;Acc:HGNC:50253]","synonyms":"hsa-mir-6804","biotype":"miRNA","ncbi_id":"102465482","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55230885,"end":55230952,"strand":-1,"description":"microRNA 6804 [Source:HGNC Symbol;Acc:HGNC:50253]"}, {"versioned_ensembl_gene_id":"ENSG00000200560.1","gene_symbol":"RNU6-288P","gene_name":"RNA, U6 small nuclear 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:47251]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479694","summary":null,"start":63573242,"end":63573345,"strand":-1,"description":"RNA, U6 small nuclear 288, pseudogene [Source:HGNC Symbol;Acc:HGNC:47251]"}, {"versioned_ensembl_gene_id":"ENSG00000199859.1","gene_symbol":"RNU6-582P","gene_name":"RNA, U6 small nuclear 582, pseudogene [Source:HGNC Symbol;Acc:HGNC:47545]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481365","summary":null,"start":157201562,"end":157201668,"strand":-1,"description":"RNA, U6 small nuclear 582, pseudogene [Source:HGNC Symbol;Acc:HGNC:47545]"}, {"versioned_ensembl_gene_id":"ENSG00000266563.1","gene_symbol":"EIF1P5","gene_name":"eukaryotic translation initiation factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49618]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481690","summary":null,"start":21259968,"end":21260501,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49618]"}, {"versioned_ensembl_gene_id":"ENSG00000207575.1","gene_symbol":"MIR649","gene_name":"microRNA 649 [Source:HGNC Symbol;Acc:HGNC:32905]","synonyms":"MIRN649,hsa-mir-649","biotype":"miRNA","ncbi_id":"693234","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21034176,"end":21034272,"strand":-1,"description":"microRNA 649 [Source:HGNC Symbol;Acc:HGNC:32905]"}, {"versioned_ensembl_gene_id":"ENSG00000271923.1","gene_symbol":"RNU6-86P","gene_name":"RNA, U6 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47049]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479604","summary":null,"start":87998229,"end":87998335,"strand":-1,"description":"RNA, U6 small nuclear 86, pseudogene [Source:HGNC Symbol;Acc:HGNC:47049]"}, {"versioned_ensembl_gene_id":"ENSG00000206989.1","gene_symbol":"SNORD63","gene_name":"small nucleolar RNA, C/D box 63 [Source:HGNC Symbol;Acc:HGNC:10220]","synonyms":"U63,SNORD63A,RNU63","biotype":"snoRNA","ncbi_id":"26785","summary":null,"start":138561043,"end":138561110,"strand":-1,"description":"small nucleolar RNA, C/D box 63 [Source:HGNC Symbol;Acc:HGNC:10220]"}, {"versioned_ensembl_gene_id":"ENSG00000273913.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42511570,"end":42511851,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000253008.2","gene_symbol":"MIR2355","gene_name":"microRNA 2355 [Source:HGNC Symbol;Acc:HGNC:38328]","synonyms":"hsa-mir-2355","biotype":"miRNA","ncbi_id":"100423036","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207109987,"end":207110073,"strand":-1,"description":"microRNA 2355 [Source:HGNC Symbol;Acc:HGNC:38328]"}, {"versioned_ensembl_gene_id":"ENSG00000239437.3","gene_symbol":"RN7SL752P","gene_name":"RNA, 7SL, cytoplasmic 752, pseudogene [Source:HGNC Symbol;Acc:HGNC:46768]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481127","summary":null,"start":129591349,"end":129591635,"strand":1,"description":"RNA, 7SL, cytoplasmic 752, pseudogene [Source:HGNC Symbol;Acc:HGNC:46768]"}, {"versioned_ensembl_gene_id":"ENSG00000252231.1","gene_symbol":"RNA5SP67","gene_name":"RNA, 5S ribosomal pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:42844]","synonyms":"RN5S67","biotype":"rRNA","ncbi_id":"100873302","summary":null,"start":173921070,"end":173921200,"strand":1,"description":"RNA, 5S ribosomal pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:42844]"}, {"versioned_ensembl_gene_id":"ENSG00000211538.1","gene_symbol":"MIR501","gene_name":"microRNA 501 [Source:HGNC Symbol;Acc:HGNC:32135]","synonyms":"MIRN501,hsa-mir-501","biotype":"miRNA","ncbi_id":"574503","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50009722,"end":50009805,"strand":1,"description":"microRNA 501 [Source:HGNC Symbol;Acc:HGNC:32135]"}, {"versioned_ensembl_gene_id":"ENSG00000265789.1","gene_symbol":"MIR4330","gene_name":"microRNA 4330 [Source:HGNC Symbol;Acc:HGNC:38273]","synonyms":"hsa-mir-4330","biotype":"miRNA","ncbi_id":"100422930","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151168222,"end":151168326,"strand":1,"description":"microRNA 4330 [Source:HGNC Symbol;Acc:HGNC:38273]"}, {"versioned_ensembl_gene_id":"ENSG00000242182.3","gene_symbol":"RN7SL745P","gene_name":"RNA, 7SL, cytoplasmic 745, pseudogene [Source:HGNC Symbol;Acc:HGNC:46761]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481858","summary":null,"start":23004564,"end":23004862,"strand":1,"description":"RNA, 7SL, cytoplasmic 745, pseudogene [Source:HGNC Symbol;Acc:HGNC:46761]"}, {"versioned_ensembl_gene_id":"ENSG00000284148.1","gene_symbol":"MIR6756","gene_name":"microRNA 6756 [Source:HGNC Symbol;Acc:HGNC:49974]","synonyms":"hsa-mir-6756","biotype":"miRNA","ncbi_id":"102465453","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119312950,"end":119313012,"strand":-1,"description":"microRNA 6756 [Source:HGNC Symbol;Acc:HGNC:49974]"}, {"versioned_ensembl_gene_id":"ENSG00000275063.1","gene_symbol":"AC233755.1","gene_name":"Immunoglobulin heavy variable 4-38-2 [Source:UniProtKB/Swiss-Prot;Acc:P0DP08]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41444,"end":41876,"strand":1,"description":"Immunoglobulin heavy variable 4-38-2 [Source:UniProtKB/Swiss-Prot;Acc:P0DP08]"}, {"versioned_ensembl_gene_id":"ENSG00000202047.1","gene_symbol":"RNA5SP324","gene_name":"RNA, 5S ribosomal pseudogene 324 [Source:HGNC Symbol;Acc:HGNC:43224]","synonyms":"RN5S324","biotype":"rRNA","ncbi_id":"100873590","summary":null,"start":96619376,"end":96619483,"strand":1,"description":"RNA, 5S ribosomal pseudogene 324 [Source:HGNC Symbol;Acc:HGNC:43224]"}, {"versioned_ensembl_gene_id":"ENSG00000198740.8","gene_symbol":"ZNF652","gene_name":"zinc finger protein 652 [Source:HGNC Symbol;Acc:HGNC:29147]","synonyms":"KIAA0924","biotype":"protein_coding","ncbi_id":"22834","summary":null,"start":49289206,"end":49362473,"strand":-1,"description":"zinc finger protein 652 [Source:HGNC Symbol;Acc:HGNC:29147]"}, {"versioned_ensembl_gene_id":"ENSG00000265213.1","gene_symbol":"MIR3684","gene_name":"microRNA 3684 [Source:HGNC Symbol;Acc:HGNC:38950]","synonyms":"hsa-mir-3684","biotype":"miRNA","ncbi_id":"100500867","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98997387,"end":98997460,"strand":1,"description":"microRNA 3684 [Source:HGNC Symbol;Acc:HGNC:38950]"}, {"versioned_ensembl_gene_id":"ENSG00000263361.1","gene_symbol":"MIR378H","gene_name":"microRNA 378h [Source:HGNC Symbol;Acc:HGNC:41744]","synonyms":"hsa-mir-378h","biotype":"miRNA","ncbi_id":"100616306","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154829458,"end":154829540,"strand":1,"description":"microRNA 378h [Source:HGNC Symbol;Acc:HGNC:41744]"}, {"versioned_ensembl_gene_id":"ENSG00000283801.1","gene_symbol":"MIR1302-11","gene_name":"microRNA 1302-11 [Source:HGNC Symbol;Acc:HGNC:38246]","synonyms":"hsa-mir-1302-11","biotype":"miRNA","ncbi_id":"100422919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71973,"end":72110,"strand":1,"description":"microRNA 1302-11 [Source:HGNC Symbol;Acc:HGNC:38246]"}, {"versioned_ensembl_gene_id":"ENSG00000264934.1","gene_symbol":"MIR4265","gene_name":"microRNA 4265 [Source:HGNC Symbol;Acc:HGNC:38358]","synonyms":"hsa-mir-4265","biotype":"miRNA","ncbi_id":"100422863","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109141490,"end":109141588,"strand":-1,"description":"microRNA 4265 [Source:HGNC Symbol;Acc:HGNC:38358]"}, {"versioned_ensembl_gene_id":"ENSG00000241807.3","gene_symbol":"RN7SL319P","gene_name":"RNA, 7SL, cytoplasmic 319, pseudogene [Source:HGNC Symbol;Acc:HGNC:46335]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479339","summary":null,"start":75785134,"end":75785354,"strand":1,"description":"RNA, 7SL, cytoplasmic 319, pseudogene [Source:HGNC Symbol;Acc:HGNC:46335]"}, {"versioned_ensembl_gene_id":"ENSG00000263432.2","gene_symbol":"RN7SL689P","gene_name":"RNA, 7SL, cytoplasmic 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:46705]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481111","summary":null,"start":123022487,"end":123022783,"strand":-1,"description":"RNA, 7SL, cytoplasmic 689, pseudogene [Source:HGNC Symbol;Acc:HGNC:46705]"}, {"versioned_ensembl_gene_id":"ENSG00000243374.3","gene_symbol":"RN7SL72P","gene_name":"RNA, 7SL, cytoplasmic 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:46088]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480941","summary":null,"start":148438309,"end":148438577,"strand":1,"description":"RNA, 7SL, cytoplasmic 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:46088]"}, {"versioned_ensembl_gene_id":"ENSG00000273621.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144739762,"end":144739941,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000207298.1","gene_symbol":"RNU6-83P","gene_name":"RNA, U6 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:42573]","synonyms":"RNU6-83","biotype":"snRNA","ncbi_id":"100873782","summary":null,"start":99025234,"end":99025345,"strand":1,"description":"RNA, U6 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:42573]"}, {"versioned_ensembl_gene_id":"ENSG00000266191.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28978391,"end":28978689,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284085.1","gene_symbol":"MIR4732","gene_name":"microRNA 4732 [Source:HGNC Symbol;Acc:HGNC:41639]","synonyms":"hsa-mir-4732","biotype":"miRNA","ncbi_id":"100616385","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28861655,"end":28861730,"strand":-1,"description":"microRNA 4732 [Source:HGNC Symbol;Acc:HGNC:41639]"}, {"versioned_ensembl_gene_id":"ENSG00000179636.14","gene_symbol":"TPPP2","gene_name":"tubulin polymerization promoting protein family member 2 [Source:HGNC Symbol;Acc:HGNC:19293]","synonyms":"p25beta,p18,CT152,C14orf8","biotype":"protein_coding","ncbi_id":"122664","summary":null,"start":21024109,"end":21036276,"strand":1,"description":"tubulin polymerization promoting protein family member 2 [Source:HGNC Symbol;Acc:HGNC:19293]"}, {"versioned_ensembl_gene_id":"ENSG00000266746.1","gene_symbol":"AC209154.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22411893,"end":22412229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236779.1","gene_symbol":"AL512306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204528845,"end":204529692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264956.1","gene_symbol":"AC138761.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22266425,"end":22288133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265110.1","gene_symbol":"MIR4731","gene_name":"microRNA 4731 [Source:HGNC Symbol;Acc:HGNC:41597]","synonyms":"hsa-mir-4731","biotype":"miRNA","ncbi_id":"100616125","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15251627,"end":15251696,"strand":-1,"description":"microRNA 4731 [Source:HGNC Symbol;Acc:HGNC:41597]"}, {"versioned_ensembl_gene_id":"ENSG00000207153.1","gene_symbol":"RNU6-933P","gene_name":"RNA, U6 small nuclear 933, pseudogene [Source:HGNC Symbol;Acc:HGNC:47896]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479979","summary":null,"start":60985061,"end":60985167,"strand":-1,"description":"RNA, U6 small nuclear 933, pseudogene [Source:HGNC Symbol;Acc:HGNC:47896]"}, {"versioned_ensembl_gene_id":"ENSG00000200473.1","gene_symbol":"RNA5SP507","gene_name":"RNA, 5S ribosomal pseudogene 507 [Source:HGNC Symbol;Acc:HGNC:43407]","synonyms":"RN5S507","biotype":"rRNA","ncbi_id":"100873558","summary":null,"start":70253042,"end":70253162,"strand":1,"description":"RNA, 5S ribosomal pseudogene 507 [Source:HGNC Symbol;Acc:HGNC:43407]"}, {"versioned_ensembl_gene_id":"ENSG00000275483.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54661303,"end":54685299,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000251754.1","gene_symbol":"RNU6-999P","gene_name":"RNA, U6 small nuclear 999, pseudogene [Source:HGNC Symbol;Acc:HGNC:47962]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480008","summary":null,"start":245043928,"end":245044032,"strand":1,"description":"RNA, U6 small nuclear 999, pseudogene [Source:HGNC Symbol;Acc:HGNC:47962]"}, {"versioned_ensembl_gene_id":"ENSG00000222178.1","gene_symbol":"RNA5SP181","gene_name":"RNA, 5S ribosomal pseudogene 181 [Source:HGNC Symbol;Acc:HGNC:43081]","synonyms":"RN5S181","biotype":"rRNA","ncbi_id":"100873443","summary":null,"start":36485343,"end":36485440,"strand":1,"description":"RNA, 5S ribosomal pseudogene 181 [Source:HGNC Symbol;Acc:HGNC:43081]"}, {"versioned_ensembl_gene_id":"ENSG00000201084.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32175247,"end":32175351,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252218.1","gene_symbol":"SCARNA15","gene_name":"Small Cajal body specific RNA 15 [Source:RFAM;Acc:RF00426]","synonyms":"ACA45,ACA45","biotype":"scaRNA","ncbi_id":"677778","summary":null,"start":43544144,"end":43544270,"strand":1,"description":"Small Cajal body specific RNA 15 [Source:RFAM;Acc:RF00426]"}, {"versioned_ensembl_gene_id":"ENSG00000263610.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30728556,"end":30728666,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252749.1","gene_symbol":"RNU7-116P","gene_name":"RNA, U7 small nuclear 116 pseudogene [Source:HGNC Symbol;Acc:HGNC:45650]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480816","summary":null,"start":63736444,"end":63736505,"strand":1,"description":"RNA, U7 small nuclear 116 pseudogene [Source:HGNC Symbol;Acc:HGNC:45650]"}, {"versioned_ensembl_gene_id":"ENSG00000200492.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":92119423,"end":92119633,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000199921.1","gene_symbol":"RNU6-161P","gene_name":"RNA, U6 small nuclear 161, pseudogene [Source:HGNC Symbol;Acc:HGNC:47124]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480387","summary":null,"start":76753135,"end":76753240,"strand":1,"description":"RNA, U6 small nuclear 161, pseudogene [Source:HGNC Symbol;Acc:HGNC:47124]"}, {"versioned_ensembl_gene_id":"ENSG00000252628.2","gene_symbol":"RNU6-453P","gene_name":"RNA, U6 small nuclear 453, pseudogene [Source:HGNC Symbol;Acc:HGNC:47416]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479766","summary":null,"start":44307088,"end":44307172,"strand":1,"description":"RNA, U6 small nuclear 453, pseudogene [Source:HGNC Symbol;Acc:HGNC:47416]"}, {"versioned_ensembl_gene_id":"ENSG00000206997.1","gene_symbol":"RNU6-524P","gene_name":"RNA, U6 small nuclear 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:47487]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481346","summary":null,"start":96210121,"end":96210227,"strand":-1,"description":"RNA, U6 small nuclear 524, pseudogene [Source:HGNC Symbol;Acc:HGNC:47487]"}, {"versioned_ensembl_gene_id":"ENSG00000265215.1","gene_symbol":"MIR4269","gene_name":"microRNA 4269 [Source:HGNC Symbol;Acc:HGNC:38291]","synonyms":"hsa-mir-4269","biotype":"miRNA","ncbi_id":"100423043","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239305462,"end":239305545,"strand":1,"description":"microRNA 4269 [Source:HGNC Symbol;Acc:HGNC:38291]"}, {"versioned_ensembl_gene_id":"ENSG00000284040.1","gene_symbol":"MIR296","gene_name":"microRNA 296 [Source:HGNC Symbol;Acc:HGNC:31617]","synonyms":"MIRN296,hsa-mir-296","biotype":"miRNA","ncbi_id":"407022","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58817615,"end":58817694,"strand":-1,"description":"microRNA 296 [Source:HGNC Symbol;Acc:HGNC:31617]"}, {"versioned_ensembl_gene_id":"ENSG00000251760.1","gene_symbol":"RNA5SP418","gene_name":"RNA, 5S ribosomal pseudogene 418 [Source:HGNC Symbol;Acc:HGNC:43318]","synonyms":"RN5S418","biotype":"rRNA","ncbi_id":"100873669","summary":null,"start":35752826,"end":35752942,"strand":1,"description":"RNA, 5S ribosomal pseudogene 418 [Source:HGNC Symbol;Acc:HGNC:43318]"}, {"versioned_ensembl_gene_id":"ENSG00000178130.9","gene_symbol":"FAM27E5","gene_name":"family with sequence similarity E5 [Source:HGNC Symbol;Acc:HGNC:32410]","synonyms":"MGC35151,FAM27L","biotype":"lincRNA","ncbi_id":"284123","summary":null,"start":22298691,"end":22299893,"strand":1,"description":"family with sequence similarity E5 [Source:HGNC Symbol;Acc:HGNC:32410]"}, {"versioned_ensembl_gene_id":"ENSG00000250071.1","gene_symbol":"AC093214.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74798994,"end":74800100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196503.3","gene_symbol":"ARL9","gene_name":"ADP ribosylation factor like GTPase 9 [Source:HGNC Symbol;Acc:HGNC:23592]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132946","summary":"ARL9 is a member of the small GTPase protein family with a high degree of similarity to ARF (MIM 103180) proteins of the RAS superfamily.[supplied by OMIM, Nov 2008]","start":56505209,"end":56524448,"strand":1,"description":"ADP ribosylation factor like GTPase 9 [Source:HGNC Symbol;Acc:HGNC:23592]"}, {"versioned_ensembl_gene_id":"ENSG00000283885.1","gene_symbol":"MIR3714","gene_name":"microRNA 3714 [Source:HGNC Symbol;Acc:HGNC:38928]","synonyms":"hsa-mir-3714","biotype":"miRNA","ncbi_id":"100500913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16933196,"end":16933260,"strand":1,"description":"microRNA 3714 [Source:HGNC Symbol;Acc:HGNC:38928]"}, {"versioned_ensembl_gene_id":"ENSG00000207954.1","gene_symbol":"MIR138-1","gene_name":"microRNA 138-1 [Source:HGNC Symbol;Acc:HGNC:31524]","synonyms":"hsa-mir-138-1,MIRN138-1","biotype":"miRNA","ncbi_id":"406929","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44114212,"end":44114310,"strand":1,"description":"microRNA 138-1 [Source:HGNC Symbol;Acc:HGNC:31524]"}, {"versioned_ensembl_gene_id":"ENSG00000207630.1","gene_symbol":"MIR7-3","gene_name":"microRNA 7-3 [Source:HGNC Symbol;Acc:HGNC:31640]","synonyms":"MIRN7-3,hsa-mir-7-3","biotype":"miRNA","ncbi_id":"407045","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4770670,"end":4770779,"strand":1,"description":"microRNA 7-3 [Source:HGNC Symbol;Acc:HGNC:31640]"}, {"versioned_ensembl_gene_id":"ENSG00000265323.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30977263,"end":30977354,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275273.1","gene_symbol":"MIR6780A","gene_name":"microRNA 6780a [Source:HGNC Symbol;Acc:HGNC:50069]","synonyms":"hsa-mir-6780a","biotype":"miRNA","ncbi_id":"102466195","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42708084,"end":42708151,"strand":-1,"description":"microRNA 6780a [Source:HGNC Symbol;Acc:HGNC:50069]"}, {"versioned_ensembl_gene_id":"ENSG00000274187.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30048502,"end":30048577,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000207325.1","gene_symbol":"RNY1P4","gene_name":"RNA, Ro-associated Y1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42481]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873804","summary":null,"start":32763438,"end":32763552,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42481]"}, {"versioned_ensembl_gene_id":"ENSG00000201967.1","gene_symbol":"RN7SKP22","gene_name":"RNA, 7SK small nuclear pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:45746]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481805","summary":null,"start":32862800,"end":32863092,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:45746]"}, {"versioned_ensembl_gene_id":"ENSG00000242638.3","gene_symbol":"RN7SL294P","gene_name":"RNA, 7SL, cytoplasmic 294, pseudogene [Source:HGNC Symbol;Acc:HGNC:46310]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479329","summary":null,"start":75182754,"end":75183048,"strand":-1,"description":"RNA, 7SL, cytoplasmic 294, pseudogene [Source:HGNC Symbol;Acc:HGNC:46310]"}, {"versioned_ensembl_gene_id":"ENSG00000207405.1","gene_symbol":"SNORA64","gene_name":"small nucleolar RNA, H/ACA box 64 [Source:HGNC Symbol;Acc:HGNC:10221]","synonyms":"RNU64,U64","biotype":"snoRNA","ncbi_id":"26784","summary":null,"start":1962973,"end":1963106,"strand":-1,"description":"small nucleolar RNA, H/ACA box 64 [Source:HGNC Symbol;Acc:HGNC:10221]"}, {"versioned_ensembl_gene_id":"ENSG00000223006.1","gene_symbol":"RN7SKP137","gene_name":"RNA, 7SK small nuclear pseudogene 137 [Source:HGNC Symbol;Acc:HGNC:45861]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479156","summary":null,"start":121061172,"end":121061478,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 137 [Source:HGNC Symbol;Acc:HGNC:45861]"}, {"versioned_ensembl_gene_id":"ENSG00000202478.1","gene_symbol":"RNU6-81P","gene_name":"RNA, U6 small nuclear 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:42571]","synonyms":"RNU6-81","biotype":"snRNA","ncbi_id":"100873780","summary":null,"start":63783801,"end":63783904,"strand":1,"description":"RNA, U6 small nuclear 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:42571]"}, {"versioned_ensembl_gene_id":"ENSG00000251919.1","gene_symbol":"RNU7-105P","gene_name":"RNA, U7 small nuclear 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:45639]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479065","summary":null,"start":72621766,"end":72621827,"strand":1,"description":"RNA, U7 small nuclear 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:45639]"}, {"versioned_ensembl_gene_id":"ENSG00000202167.1","gene_symbol":"RNU1-114P","gene_name":"RNA, U1 small nuclear 114, pseudogene [Source:HGNC Symbol;Acc:HGNC:48456]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481626","summary":null,"start":143652050,"end":143652215,"strand":-1,"description":"RNA, U1 small nuclear 114, pseudogene [Source:HGNC Symbol;Acc:HGNC:48456]"}, {"versioned_ensembl_gene_id":"ENSG00000243546.3","gene_symbol":"RN7SL108P","gene_name":"RNA, 7SL, cytoplasmic 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:46124]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480950","summary":null,"start":68236243,"end":68236539,"strand":-1,"description":"RNA, 7SL, cytoplasmic 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:46124]"}, {"versioned_ensembl_gene_id":"ENSG00000274547.1","gene_symbol":"Six3os1_6","gene_name":"Six3os1 conserved region 6 [Source:RFAM;Acc:RF02251]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44938833,"end":44939028,"strand":1,"description":"Six3os1 conserved region 6 [Source:RFAM;Acc:RF02251]"}, {"versioned_ensembl_gene_id":"ENSG00000251773.1","gene_symbol":"RNU6-1129P","gene_name":"RNA, U6 small nuclear 1129, pseudogene [Source:HGNC Symbol;Acc:HGNC:48092]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481536","summary":null,"start":86235321,"end":86235424,"strand":1,"description":"RNA, U6 small nuclear 1129, pseudogene [Source:HGNC Symbol;Acc:HGNC:48092]"}, {"versioned_ensembl_gene_id":"ENSG00000201179.1","gene_symbol":"RNU6-1322P","gene_name":"RNA, U6 small nuclear 1322, pseudogene [Source:HGNC Symbol;Acc:HGNC:48285]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480143","summary":null,"start":105332790,"end":105332896,"strand":1,"description":"RNA, U6 small nuclear 1322, pseudogene [Source:HGNC Symbol;Acc:HGNC:48285]"}, {"versioned_ensembl_gene_id":"ENSG00000283420.1","gene_symbol":"MIR4278","gene_name":"microRNA 4278 [Source:HGNC Symbol;Acc:HGNC:38243]","synonyms":"hsa-mir-4278","biotype":"miRNA","ncbi_id":"100422999","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6827853,"end":6827921,"strand":-1,"description":"microRNA 4278 [Source:HGNC Symbol;Acc:HGNC:38243]"}, {"versioned_ensembl_gene_id":"ENSG00000238297.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":107999791,"end":107999982,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000264084.1","gene_symbol":"MIR5688","gene_name":"microRNA 5688 [Source:HGNC Symbol;Acc:HGNC:43463]","synonyms":"hsa-mir-5688","biotype":"miRNA","ncbi_id":"100847077","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85385710,"end":85385792,"strand":1,"description":"microRNA 5688 [Source:HGNC Symbol;Acc:HGNC:43463]"}, {"versioned_ensembl_gene_id":"ENSG00000252888.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":76835377,"end":76835502,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000265252.1","gene_symbol":"MIR3132","gene_name":"microRNA 3132 [Source:HGNC Symbol;Acc:HGNC:38373]","synonyms":"hsa-mir-3132","biotype":"miRNA","ncbi_id":"100423039","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219549073,"end":219549147,"strand":-1,"description":"microRNA 3132 [Source:HGNC Symbol;Acc:HGNC:38373]"}, {"versioned_ensembl_gene_id":"ENSG00000266078.1","gene_symbol":"MIR4432","gene_name":"microRNA 4432 [Source:HGNC Symbol;Acc:HGNC:41649]","synonyms":"hsa-mir-4432","biotype":"miRNA","ncbi_id":"100616473","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60387362,"end":60387445,"strand":-1,"description":"microRNA 4432 [Source:HGNC Symbol;Acc:HGNC:41649]"}, {"versioned_ensembl_gene_id":"ENSG00000284034.1","gene_symbol":"MIR5196","gene_name":"microRNA 5196 [Source:HGNC Symbol;Acc:HGNC:43542]","synonyms":"hsa-mir-5196","biotype":"miRNA","ncbi_id":"100847070","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35345513,"end":35345627,"strand":1,"description":"microRNA 5196 [Source:HGNC Symbol;Acc:HGNC:43542]"}, {"versioned_ensembl_gene_id":"ENSG00000275640.1","gene_symbol":"MIR6793","gene_name":"microRNA 6793 [Source:HGNC Symbol;Acc:HGNC:50251]","synonyms":"hsa-mir-6793","biotype":"miRNA","ncbi_id":"102466737","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10828973,"end":10829035,"strand":1,"description":"microRNA 6793 [Source:HGNC Symbol;Acc:HGNC:50251]"}, {"versioned_ensembl_gene_id":"ENSG00000274127.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":146208665,"end":146208819,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000244116.3","gene_symbol":"IGKV2-28","gene_name":"immunoglobulin kappa variable 2-28 [Source:HGNC Symbol;Acc:HGNC:5783]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28921","summary":null,"start":89221698,"end":89222461,"strand":-1,"description":"immunoglobulin kappa variable 2-28 [Source:HGNC Symbol;Acc:HGNC:5783]"}, {"versioned_ensembl_gene_id":"ENSG00000263409.1","gene_symbol":"MIR4747","gene_name":"microRNA 4747 [Source:HGNC Symbol;Acc:HGNC:41827]","synonyms":"hsa-mir-4747","biotype":"miRNA","ncbi_id":"100616337","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4932687,"end":4932740,"strand":1,"description":"microRNA 4747 [Source:HGNC Symbol;Acc:HGNC:41827]"}, {"versioned_ensembl_gene_id":"ENSG00000200428.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50743568,"end":50743684,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275213.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":205684018,"end":205684307,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000274475.1","gene_symbol":"RN7SL650P","gene_name":"RNA, 7SL, cytoplasmic 650, pseudogene [Source:HGNC Symbol;Acc:HGNC:46666]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480523","summary":null,"start":21429508,"end":21429806,"strand":-1,"description":"RNA, 7SL, cytoplasmic 650, pseudogene [Source:HGNC Symbol;Acc:HGNC:46666]"}, {"versioned_ensembl_gene_id":"ENSG00000238788.1","gene_symbol":"RNU7-182P","gene_name":"RNA, U7 small nuclear 182 pseudogene [Source:HGNC Symbol;Acc:HGNC:45716]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480831","summary":null,"start":127017421,"end":127017482,"strand":1,"description":"RNA, U7 small nuclear 182 pseudogene [Source:HGNC Symbol;Acc:HGNC:45716]"}, {"versioned_ensembl_gene_id":"ENSG00000200475.1","gene_symbol":"RN7SKP162","gene_name":"RNA, 7SK small nuclear pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:45886]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480884","summary":null,"start":13683542,"end":13683886,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 162 [Source:HGNC Symbol;Acc:HGNC:45886]"}, {"versioned_ensembl_gene_id":"ENSG00000199630.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":89841329,"end":89841424,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273614.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"SNORA11A,U107","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":7826098,"end":7826225,"strand":-1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000276956.1","gene_symbol":"RN7SL769P","gene_name":"RNA, 7SL, cytoplasmic 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:46785]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479502","summary":null,"start":110360452,"end":110360746,"strand":-1,"description":"RNA, 7SL, cytoplasmic 769, pseudogene [Source:HGNC Symbol;Acc:HGNC:46785]"}, {"versioned_ensembl_gene_id":"ENSG00000276088.1","gene_symbol":"RN7SL620P","gene_name":"RNA, 7SL, cytoplasmic 620, pseudogene [Source:HGNC Symbol;Acc:HGNC:46636]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479448","summary":null,"start":16710059,"end":16710361,"strand":1,"description":"RNA, 7SL, cytoplasmic 620, pseudogene [Source:HGNC Symbol;Acc:HGNC:46636]"}, {"versioned_ensembl_gene_id":"ENSG00000222630.2","gene_symbol":"RN7SKP131","gene_name":"RNA, 7SK small nuclear pseudogene 131 [Source:HGNC Symbol;Acc:HGNC:45855]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479153","summary":null,"start":18605802,"end":18606102,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 131 [Source:HGNC Symbol;Acc:HGNC:45855]"}, {"versioned_ensembl_gene_id":"ENSG00000283469.1","gene_symbol":"MIR3130-1","gene_name":"microRNA 3130-1 [Source:HGNC Symbol;Acc:HGNC:38275]","synonyms":"MIR3130-3,hsa-mir-3130-3,hsa-mir-3130-1","biotype":"miRNA","ncbi_id":"100422993","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":206783234,"end":206783308,"strand":-1,"description":"microRNA 3130-1 [Source:HGNC Symbol;Acc:HGNC:38275]"}, {"versioned_ensembl_gene_id":"ENSG00000221430.1","gene_symbol":"MIR1294","gene_name":"microRNA 1294 [Source:HGNC Symbol;Acc:HGNC:35287]","synonyms":"MIRN1294,hsa-mir-1294","biotype":"miRNA","ncbi_id":"100302181","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154347106,"end":154347247,"strand":1,"description":"microRNA 1294 [Source:HGNC Symbol;Acc:HGNC:35287]"}, {"versioned_ensembl_gene_id":"ENSG00000207788.1","gene_symbol":"MIR519C","gene_name":"microRNA 519c [Source:HGNC Symbol;Acc:HGNC:32098]","synonyms":"hsa-mir-519c,MIRN519C","biotype":"miRNA","ncbi_id":"574466","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53686469,"end":53686555,"strand":1,"description":"microRNA 519c [Source:HGNC Symbol;Acc:HGNC:32098]"}, {"versioned_ensembl_gene_id":"ENSG00000239625.3","gene_symbol":"RN7SL241P","gene_name":"RNA, 7SL, cytoplasmic 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:46257]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480988","summary":null,"start":30366064,"end":30366299,"strand":-1,"description":"RNA, 7SL, cytoplasmic 241, pseudogene [Source:HGNC Symbol;Acc:HGNC:46257]"}, {"versioned_ensembl_gene_id":"ENSG00000277475.1","gene_symbol":"AC213203.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31698,"end":32528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149548.14","gene_symbol":"CCDC15","gene_name":"coiled-coil domain containing 15 [Source:HGNC Symbol;Acc:HGNC:25798]","synonyms":"FLJ13215","biotype":"protein_coding","ncbi_id":"80071","summary":null,"start":124954121,"end":125041489,"strand":1,"description":"coiled-coil domain containing 15 [Source:HGNC Symbol;Acc:HGNC:25798]"}, {"versioned_ensembl_gene_id":"ENSG00000270710.1","gene_symbol":"FO393422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235565761,"end":235566937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283685.1","gene_symbol":"MIR522","gene_name":"microRNA 522 [Source:HGNC Symbol;Acc:HGNC:32127]","synonyms":"MIRN522,hsa-mir-522","biotype":"miRNA","ncbi_id":"574495","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53751211,"end":53751297,"strand":1,"description":"microRNA 522 [Source:HGNC Symbol;Acc:HGNC:32127]"}, {"versioned_ensembl_gene_id":"ENSG00000266325.1","gene_symbol":"MIR3665","gene_name":"microRNA 3665 [Source:HGNC Symbol;Acc:HGNC:38939]","synonyms":"hsa-mir-3665","biotype":"miRNA","ncbi_id":"100500861","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77698012,"end":77698116,"strand":-1,"description":"microRNA 3665 [Source:HGNC Symbol;Acc:HGNC:38939]"}, {"versioned_ensembl_gene_id":"ENSG00000208027.4","gene_symbol":"MIR485","gene_name":"microRNA 485 [Source:HGNC Symbol;Acc:HGNC:32067]","synonyms":"MIRN485,hsa-mir-485","biotype":"miRNA","ncbi_id":"574436","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101055419,"end":101055491,"strand":1,"description":"microRNA 485 [Source:HGNC Symbol;Acc:HGNC:32067]"}, {"versioned_ensembl_gene_id":"ENSG00000200874.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75513025,"end":75513126,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275305.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":30816156,"end":30816274,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000207355.1","gene_symbol":"RNU6-1257P","gene_name":"RNA, U6 small nuclear 1257, pseudogene [Source:HGNC Symbol;Acc:HGNC:48220]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481577","summary":null,"start":24974171,"end":24974280,"strand":1,"description":"RNA, U6 small nuclear 1257, pseudogene [Source:HGNC Symbol;Acc:HGNC:48220]"}, {"versioned_ensembl_gene_id":"ENSG00000244297.3","gene_symbol":"RN7SL465P","gene_name":"RNA, 7SL, cytoplasmic 465, pseudogene [Source:HGNC Symbol;Acc:HGNC:46481]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479392","summary":null,"start":38744086,"end":38744386,"strand":1,"description":"RNA, 7SL, cytoplasmic 465, pseudogene [Source:HGNC Symbol;Acc:HGNC:46481]"}, {"versioned_ensembl_gene_id":"ENSG00000202433.1","gene_symbol":"RNU6-54P","gene_name":"RNA, U6 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:42544]","synonyms":"RNU6-54","biotype":"snRNA","ncbi_id":"106478986","summary":null,"start":70459464,"end":70459570,"strand":1,"description":"RNA, U6 small nuclear 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:42544]"}, {"versioned_ensembl_gene_id":"ENSG00000212569.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50669804,"end":50669901,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276861.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":89600571,"end":89600680,"strand":1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000239948.2","gene_symbol":"RN7SL368P","gene_name":"RNA, 7SL, cytoplasmic 368, pseudogene [Source:HGNC Symbol;Acc:HGNC:46384]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479357","summary":null,"start":43660500,"end":43660776,"strand":-1,"description":"RNA, 7SL, cytoplasmic 368, pseudogene [Source:HGNC Symbol;Acc:HGNC:46384]"}, {"versioned_ensembl_gene_id":"ENSG00000274234.1","gene_symbol":"RN7SL818P","gene_name":"RNA, 7SL, cytoplasmic 818, pseudogene [Source:HGNC Symbol;Acc:HGNC:46834]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479520","summary":null,"start":24210958,"end":24211216,"strand":-1,"description":"RNA, 7SL, cytoplasmic 818, pseudogene [Source:HGNC Symbol;Acc:HGNC:46834]"}, {"versioned_ensembl_gene_id":"ENSG00000200999.1","gene_symbol":"SNORD74","gene_name":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]","synonyms":null,"biotype":"snoRNA","ncbi_id":"619498","summary":null,"start":26702309,"end":26702388,"strand":1,"description":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]"}, {"versioned_ensembl_gene_id":"ENSG00000207493.1","gene_symbol":"SNORA46","gene_name":"small nucleolar RNA, H/ACA box 46 [Source:HGNC Symbol;Acc:HGNC:32639]","synonyms":"ACA46","biotype":"snoRNA","ncbi_id":"677827","summary":null,"start":58548499,"end":58548633,"strand":-1,"description":"small nucleolar RNA, H/ACA box 46 [Source:HGNC Symbol;Acc:HGNC:32639]"}, {"versioned_ensembl_gene_id":"ENSG00000262704.1","gene_symbol":"RNU4-45P","gene_name":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481186","summary":null,"start":22205192,"end":22205332,"strand":1,"description":"RNA, U4 small nuclear 45, pseudogene [Source:HGNC Symbol;Acc:HGNC:46981]"}, {"versioned_ensembl_gene_id":"ENSG00000239494.2","gene_symbol":"RN7SL333P","gene_name":"RNA, 7SL, cytoplasmic 333, pseudogene [Source:HGNC Symbol;Acc:HGNC:46349]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481014","summary":null,"start":169859756,"end":169860052,"strand":1,"description":"RNA, 7SL, cytoplasmic 333, pseudogene [Source:HGNC Symbol;Acc:HGNC:46349]"}, {"versioned_ensembl_gene_id":"ENSG00000206852.1","gene_symbol":"RNU6-895P","gene_name":"RNA, U6 small nuclear 895, pseudogene [Source:HGNC Symbol;Acc:HGNC:47858]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479962","summary":null,"start":41298163,"end":41298265,"strand":1,"description":"RNA, U6 small nuclear 895, pseudogene [Source:HGNC Symbol;Acc:HGNC:47858]"}, {"versioned_ensembl_gene_id":"ENSG00000251819.1","gene_symbol":"RNU6-322P","gene_name":"RNA, U6 small nuclear 322, pseudogene [Source:HGNC Symbol;Acc:HGNC:47285]","synonyms":null,"biotype":"snRNA","ncbi_id":"107105253","summary":null,"start":100551820,"end":100551922,"strand":-1,"description":"RNA, U6 small nuclear 322, pseudogene [Source:HGNC Symbol;Acc:HGNC:47285]"}, {"versioned_ensembl_gene_id":"ENSG00000265327.2","gene_symbol":"RN7SL411P","gene_name":"RNA, 7SL, cytoplasmic 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:46427]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481035","summary":null,"start":40209005,"end":40209304,"strand":1,"description":"RNA, 7SL, cytoplasmic 411, pseudogene [Source:HGNC Symbol;Acc:HGNC:46427]"}, {"versioned_ensembl_gene_id":"ENSG00000278746.1","gene_symbol":"RN7SL660P","gene_name":"RNA, 7SL, cytoplasmic 660, pseudogene [Source:HGNC Symbol;Acc:HGNC:46676]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479463","summary":null,"start":32442341,"end":32442639,"strand":1,"description":"RNA, 7SL, cytoplasmic 660, pseudogene [Source:HGNC Symbol;Acc:HGNC:46676]"}, {"versioned_ensembl_gene_id":"ENSG00000200637.1","gene_symbol":"RNU5F-3P","gene_name":"RNA, U5F small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42514]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873866","summary":null,"start":6017723,"end":6017839,"strand":-1,"description":"RNA, U5F small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42514]"}, {"versioned_ensembl_gene_id":"ENSG00000086827.8","gene_symbol":"ZW10","gene_name":"zw10 kinetochore protein [Source:HGNC Symbol;Acc:HGNC:13194]","synonyms":"KNTC1AP","biotype":"protein_coding","ncbi_id":"9183","summary":"This gene encodes a protein that is one of many involved in mechanisms to ensure proper chromosome segregation during cell division. This protein is an essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. [provided by RefSeq, Aug 2011]","start":113733187,"end":113773811,"strand":-1,"description":"zw10 kinetochore protein [Source:HGNC Symbol;Acc:HGNC:13194]"}, {"versioned_ensembl_gene_id":"ENSG00000207642.1","gene_symbol":"MIR571","gene_name":"microRNA 571 [Source:HGNC Symbol;Acc:HGNC:32827]","synonyms":"MIRN571,hsa-mir-571","biotype":"miRNA","ncbi_id":"693156","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":350157,"end":350252,"strand":1,"description":"microRNA 571 [Source:HGNC Symbol;Acc:HGNC:32827]"}, {"versioned_ensembl_gene_id":"ENSG00000283441.1","gene_symbol":"MIR499B","gene_name":"microRNA 499b [Source:HGNC Symbol;Acc:HGNC:41640]","synonyms":"hsa-mir-499a,MIR499A","biotype":"miRNA","ncbi_id":"100616134","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34990400,"end":34990472,"strand":-1,"description":"microRNA 499b [Source:HGNC Symbol;Acc:HGNC:41640]"}, {"versioned_ensembl_gene_id":"ENSG00000252212.1","gene_symbol":"RNU2-58P","gene_name":"RNA, U2 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:48551]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481652","summary":null,"start":59129276,"end":59129458,"strand":-1,"description":"RNA, U2 small nuclear 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:48551]"}, {"versioned_ensembl_gene_id":"ENSG00000271739.1","gene_symbol":"RNU1-29P","gene_name":"RNA, U1 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:48371]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480154","summary":null,"start":120005976,"end":120006101,"strand":-1,"description":"RNA, U1 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:48371]"}, {"versioned_ensembl_gene_id":"ENSG00000201501.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50563009,"end":50563110,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222693.1","gene_symbol":"RN7SKP120","gene_name":"RNA, 7SK small nuclear pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:45844]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480870","summary":null,"start":25088811,"end":25089151,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 120 [Source:HGNC Symbol;Acc:HGNC:45844]"}, {"versioned_ensembl_gene_id":"ENSG00000199331.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":109042386,"end":109042487,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200534.1","gene_symbol":"SNORA33","gene_name":"small nucleolar RNA, H/ACA box 33 [Source:HGNC Symbol;Acc:HGNC:32623]","synonyms":"ACA33","biotype":"snoRNA","ncbi_id":"594839","summary":null,"start":132817219,"end":132817348,"strand":1,"description":"small nucleolar RNA, H/ACA box 33 [Source:HGNC Symbol;Acc:HGNC:32623]"}, {"versioned_ensembl_gene_id":"ENSG00000252083.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":23972188,"end":23972294,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000202414.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":25214698,"end":25214798,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212024.2","gene_symbol":"MIR550A3","gene_name":"microRNA 550a-3 [Source:HGNC Symbol;Acc:HGNC:41870]","synonyms":"hsa-mir-550a-3","biotype":"miRNA","ncbi_id":"100616354","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29680734,"end":29680828,"strand":-1,"description":"microRNA 550a-3 [Source:HGNC Symbol;Acc:HGNC:41870]"}, {"versioned_ensembl_gene_id":"ENSG00000243136.3","gene_symbol":"RN7SL22P","gene_name":"RNA, 7SL, cytoplasmic 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46038]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480928","summary":null,"start":35671776,"end":35672044,"strand":1,"description":"RNA, 7SL, cytoplasmic 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46038]"}, {"versioned_ensembl_gene_id":"ENSG00000276176.1","gene_symbol":"MIR6090","gene_name":"microRNA 6090 [Source:HGNC Symbol;Acc:HGNC:50204]","synonyms":"hsa-mir-6090","biotype":"miRNA","ncbi_id":"102466104","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128522390,"end":128522449,"strand":1,"description":"microRNA 6090 [Source:HGNC Symbol;Acc:HGNC:50204]"}, {"versioned_ensembl_gene_id":"ENSG00000284458.1","gene_symbol":"MIR1304","gene_name":"microRNA 1304 [Source:HGNC Symbol;Acc:HGNC:35302]","synonyms":"MIRN1304,hsa-mir-1304","biotype":"miRNA","ncbi_id":"100302240","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93733674,"end":93733764,"strand":-1,"description":"microRNA 1304 [Source:HGNC Symbol;Acc:HGNC:35302]"}, {"versioned_ensembl_gene_id":"ENSG00000248474.1","gene_symbol":"LINC02122","gene_name":"long intergenic non-protein coding RNA 2122 [Source:HGNC Symbol;Acc:HGNC:52979]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379036","summary":null,"start":74084068,"end":74103216,"strand":-1,"description":"long intergenic non-protein coding RNA 2122 [Source:HGNC Symbol;Acc:HGNC:52979]"}, {"versioned_ensembl_gene_id":"ENSG00000283688.1","gene_symbol":"MIR6715B","gene_name":"microRNA 6715b [Source:HGNC Symbol;Acc:HGNC:50249]","synonyms":"hsa-mir-6715b","biotype":"miRNA","ncbi_id":"102465427","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112299612,"end":112299688,"strand":-1,"description":"microRNA 6715b [Source:HGNC Symbol;Acc:HGNC:50249]"}, {"versioned_ensembl_gene_id":"ENSG00000216035.1","gene_symbol":"MIR938","gene_name":"microRNA 938 [Source:HGNC Symbol;Acc:HGNC:33681]","synonyms":"MIRN938,hsa-mir-938","biotype":"miRNA","ncbi_id":"100126327","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29602264,"end":29602346,"strand":-1,"description":"microRNA 938 [Source:HGNC Symbol;Acc:HGNC:33681]"}, {"versioned_ensembl_gene_id":"ENSG00000199564.1","gene_symbol":"RNA5SP502","gene_name":"RNA, 5S ribosomal pseudogene 502 [Source:HGNC Symbol;Acc:HGNC:43402]","synonyms":"RN5S502","biotype":"rRNA","ncbi_id":"100873553","summary":null,"start":41292798,"end":41292916,"strand":1,"description":"RNA, 5S ribosomal pseudogene 502 [Source:HGNC Symbol;Acc:HGNC:43402]"}, {"versioned_ensembl_gene_id":"ENSG00000274418.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":54972739,"end":54991632,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000252980.1","gene_symbol":"RNU6-367P","gene_name":"RNA, U6 small nuclear 367, pseudogene [Source:HGNC Symbol;Acc:HGNC:47330]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481890","summary":null,"start":44071087,"end":44071186,"strand":1,"description":"RNA, U6 small nuclear 367, pseudogene [Source:HGNC Symbol;Acc:HGNC:47330]"}, {"versioned_ensembl_gene_id":"ENSG00000222287.1","gene_symbol":"RNU6-1043P","gene_name":"RNA, U6 small nuclear 1043, pseudogene [Source:HGNC Symbol;Acc:HGNC:48006]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481510","summary":null,"start":30701337,"end":30701435,"strand":-1,"description":"RNA, U6 small nuclear 1043, pseudogene [Source:HGNC Symbol;Acc:HGNC:48006]"}, {"versioned_ensembl_gene_id":"ENSG00000242976.3","gene_symbol":"RN7SL177P","gene_name":"RNA, 7SL, cytoplasmic 177, pseudogene [Source:HGNC Symbol;Acc:HGNC:46193]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480969","summary":null,"start":153755382,"end":153755680,"strand":1,"description":"RNA, 7SL, cytoplasmic 177, pseudogene [Source:HGNC Symbol;Acc:HGNC:46193]"}, {"versioned_ensembl_gene_id":"ENSG00000281230.2","gene_symbol":"SERTAD4","gene_name":"SERTA domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25236]","synonyms":"DJ667H12.2","biotype":"protein_coding","ncbi_id":"56256","summary":null,"start":210232799,"end":210246631,"strand":1,"description":"SERTA domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25236]"}, {"versioned_ensembl_gene_id":"ENSG00000253083.1","gene_symbol":"RNA5SP106","gene_name":"RNA, 5S ribosomal pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:42904]","synonyms":"RN5S106","biotype":"rRNA","ncbi_id":"106478994","summary":null,"start":147713455,"end":147713554,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 106 [Source:HGNC Symbol;Acc:HGNC:42904]"}, {"versioned_ensembl_gene_id":"ENSG00000253027.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":44764950,"end":44765100,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000222445.1","gene_symbol":"RN7SKP56","gene_name":"RNA, 7SK small nuclear pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:45780]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481807","summary":null,"start":125875168,"end":125875498,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:45780]"}, {"versioned_ensembl_gene_id":"ENSG00000223197.1","gene_symbol":"RNU6-1001P","gene_name":"RNA, U6 small nuclear 1001, pseudogene [Source:HGNC Symbol;Acc:HGNC:47964]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480628","summary":null,"start":155089439,"end":155089538,"strand":-1,"description":"RNA, U6 small nuclear 1001, pseudogene [Source:HGNC Symbol;Acc:HGNC:47964]"}, {"versioned_ensembl_gene_id":"ENSG00000201170.1","gene_symbol":"RNU1-132P","gene_name":"RNA, U1 small nuclear 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:48474]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481958","summary":null,"start":245133927,"end":245134090,"strand":-1,"description":"RNA, U1 small nuclear 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:48474]"}, {"versioned_ensembl_gene_id":"ENSG00000252104.1","gene_symbol":"RNU6-191P","gene_name":"RNA, U6 small nuclear 191, pseudogene [Source:HGNC Symbol;Acc:HGNC:47154]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479651","summary":null,"start":64397694,"end":64397787,"strand":-1,"description":"RNA, U6 small nuclear 191, pseudogene [Source:HGNC Symbol;Acc:HGNC:47154]"}, {"versioned_ensembl_gene_id":"ENSG00000227059.6","gene_symbol":"ANHX","gene_name":"anomalous homeobox [Source:HGNC Symbol;Acc:HGNC:40024]","synonyms":null,"biotype":"protein_coding","ncbi_id":"647589","summary":null,"start":133218312,"end":133236095,"strand":-1,"description":"anomalous homeobox [Source:HGNC Symbol;Acc:HGNC:40024]"}, {"versioned_ensembl_gene_id":"ENSG00000258857.1","gene_symbol":"AL359397.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50397013,"end":50398345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100490.9","gene_symbol":"CDKL1","gene_name":"cyclin dependent kinase like 1 [Source:HGNC Symbol;Acc:HGNC:1781]","synonyms":"KKIALRE","biotype":"protein_coding","ncbi_id":"8814","summary":"This gene product is a member of a large family of CDC2-related serine/threonine protein kinases that accumulates primarily in the nucleus. [provided by RefSeq, Nov 2018]","start":50329404,"end":50416461,"strand":-1,"description":"cyclin dependent kinase like 1 [Source:HGNC Symbol;Acc:HGNC:1781]"}, {"versioned_ensembl_gene_id":"ENSG00000125375.14","gene_symbol":"ATP5S","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit s (factor B) [Source:HGNC Symbol;Acc:HGNC:18799]","synonyms":"HSU79253,ATPW","biotype":"protein_coding","ncbi_id":"27109","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. This gene encodes the subunit s, also known as factor B, of the proton channel. This subunit is necessary for the energy transduction activity of the ATP synthase complexes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":50312326,"end":50335558,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit s (factor B) [Source:HGNC Symbol;Acc:HGNC:18799]"}, {"versioned_ensembl_gene_id":"ENSG00000087299.11","gene_symbol":"L2HGDH","gene_name":"L-2-hydroxyglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:20499]","synonyms":"FLJ12618,C14orf160","biotype":"protein_coding","ncbi_id":"79944","summary":"This gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe cognitive disability. [provided by RefSeq, Jul 2008]","start":50237563,"end":50312548,"strand":-1,"description":"L-2-hydroxyglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:20499]"}, {"versioned_ensembl_gene_id":"ENSG00000250761.2","gene_symbol":"AC093305.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7707802,"end":7749766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165795.23","gene_symbol":"NDRG2","gene_name":"NDRG family member 2 [Source:HGNC Symbol;Acc:HGNC:14460]","synonyms":"SYLD,KIAA1248","biotype":"protein_coding","ncbi_id":"57447","summary":"This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein that may play a role in neurite outgrowth. This gene may be involved in glioblastoma carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":21016763,"end":21070872,"strand":-1,"description":"NDRG family member 2 [Source:HGNC Symbol;Acc:HGNC:14460]"}, {"versioned_ensembl_gene_id":"ENSG00000264769.1","gene_symbol":"AC145207.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81922899,"end":81924511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239602.1","gene_symbol":"AC091959.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146137755,"end":146138381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262831.1","gene_symbol":"AC145207.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81843165,"end":81843958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185624.14","gene_symbol":"P4HB","gene_name":"prolyl 4-hydroxylase subunit beta [Source:HGNC Symbol;Acc:HGNC:8548]","synonyms":"ERBA2L,DSI,PROHB,PO4HB,PO4DB,PDIA1,PDI,P4Hbeta,GIT","biotype":"protein_coding","ncbi_id":"5034","summary":"This gene encodes the beta subunit of prolyl 4-hydroxylase, a highly abundant multifunctional enzyme that belongs to the protein disulfide isomerase family. When present as a tetramer consisting of two alpha and two beta subunits, this enzyme is involved in hydroxylation of prolyl residues in preprocollagen. This enzyme is also a disulfide isomerase containing two thioredoxin domains that catalyze the formation, breakage and rearrangement of disulfide bonds. Other known functions include its ability to act as a chaperone that inhibits aggregation of misfolded proteins in a concentration-dependent manner, its ability to bind thyroid hormone, its role in both the influx and efflux of S-nitrosothiol-bound nitric oxide, and its function as a subunit of the microsomal triglyceride transfer protein complex. [provided by RefSeq, Jul 2008]","start":81843159,"end":81860694,"strand":-1,"description":"prolyl 4-hydroxylase subunit beta [Source:HGNC Symbol;Acc:HGNC:8548]"}, {"versioned_ensembl_gene_id":"ENSG00000247416.2","gene_symbol":"AP000802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112959279,"end":112963460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164325.7","gene_symbol":"TMEM174","gene_name":"transmembrane protein 174 [Source:HGNC Symbol;Acc:HGNC:28187]","synonyms":"MGC13034,FLJ31268","biotype":"protein_coding","ncbi_id":"134288","summary":null,"start":73173195,"end":73175143,"strand":1,"description":"transmembrane protein 174 [Source:HGNC Symbol;Acc:HGNC:28187]"}, {"versioned_ensembl_gene_id":"ENSG00000279679.1","gene_symbol":"AC091925.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":143375628,"end":143375883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100479.12","gene_symbol":"POLE2","gene_name":"DNA polymerase epsilon 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9178]","synonyms":"DPE2","biotype":"protein_coding","ncbi_id":"5427","summary":"DNA polymerase epsilon, which is involved in DNA repair and replication, is composed of a large catalytic subunit and a small accessory subunit. The protein encoded by this gene represents the small subunit (B). Defects in this gene have been linked to colorectal cancer and to combined immunodeficiency. [provided by RefSeq, Jan 2017]","start":49643555,"end":49688422,"strand":-1,"description":"DNA polymerase epsilon 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9178]"}, {"versioned_ensembl_gene_id":"ENSG00000058668.14","gene_symbol":"ATP2B4","gene_name":"ATPase plasma membrane Ca2+ transporting 4 [Source:HGNC Symbol;Acc:HGNC:817]","synonyms":"PMCA4,MXRA1,ATP2B2","biotype":"protein_coding","ncbi_id":"493","summary":"The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 4. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":203626561,"end":203744081,"strand":1,"description":"ATPase plasma membrane Ca2+ transporting 4 [Source:HGNC Symbol;Acc:HGNC:817]"}, {"versioned_ensembl_gene_id":"ENSG00000253965.1","gene_symbol":"AC008438.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140348484,"end":140357794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237342.1","gene_symbol":"AL132796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98844896,"end":98845597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120051.14","gene_symbol":"CFAP58","gene_name":"cilia and flagella associated protein 58 [Source:HGNC Symbol;Acc:HGNC:26676]","synonyms":"FLJ35908,CCDC147,C10orf80,bA554P13.1","biotype":"protein_coding","ncbi_id":"159686","summary":null,"start":104353764,"end":104455090,"strand":1,"description":"cilia and flagella associated protein 58 [Source:HGNC Symbol;Acc:HGNC:26676]"}, {"versioned_ensembl_gene_id":"ENSG00000254528.7","gene_symbol":"AP000757.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117833719,"end":117838942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263167.1","gene_symbol":"AC115099.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81135771,"end":81136256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157107.13","gene_symbol":"FCHO2","gene_name":"FCH domain only 2 [Source:HGNC Symbol;Acc:HGNC:25180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115548","summary":null,"start":72955981,"end":73090522,"strand":1,"description":"FCH domain only 2 [Source:HGNC Symbol;Acc:HGNC:25180]"}, {"versioned_ensembl_gene_id":"ENSG00000171777.15","gene_symbol":"RASGRP4","gene_name":"RAS guanyl releasing protein 4 [Source:HGNC Symbol;Acc:HGNC:18958]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115727","summary":"The protein encoded by this gene is a member of the Ras guanyl nucleotide-releasing protein (RasGRP) family of Ras guanine nucleotide exchange factors. It contains a Ras exchange motif, a diacylglycerol-binding domain, and two calcium-binding EF hands. This protein was shown to activate H-Ras in a cation-dependent manner in vitro. Expression of this protein in myeloid cell lines was found to be correlated with elevated level of activated RAS protein, and the RAS activation can be greatly enhanced by phorbol ester treatment, which suggested a role of this protein in diacylglycerol regulated cell signaling pathways. Studies of a mast cell leukemia cell line expressing substantial amounts of abnormal transcripts of this gene indicated that this gene may play an important role in the final stages of mast cell development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]","start":38409051,"end":38426305,"strand":-1,"description":"RAS guanyl releasing protein 4 [Source:HGNC Symbol;Acc:HGNC:18958]"}, {"versioned_ensembl_gene_id":"ENSG00000272639.1","gene_symbol":"AC015712.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":100861924,"end":100885329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185129.5","gene_symbol":"PURA","gene_name":"purine rich element binding protein A [Source:HGNC Symbol;Acc:HGNC:9701]","synonyms":"PURALPHA,PUR1,PUR-ALPHA","biotype":"protein_coding","ncbi_id":"5813","summary":"This gene product is a sequence-specific, single-stranded DNA-binding protein. It binds preferentially to the single strand of the purine-rich element termed PUR, which is present at origins of replication and in gene flanking regions in a variety of eukaryotes from yeasts through humans. Thus, it is implicated in the control of both DNA replication and transcription. Deletion of this gene has been associated with myelodysplastic syndrome and acute myelogenous leukemia. [provided by RefSeq, Jul 2008]","start":140107777,"end":140125619,"strand":1,"description":"purine rich element binding protein A [Source:HGNC Symbol;Acc:HGNC:9701]"}, {"versioned_ensembl_gene_id":"ENSG00000266042.1","gene_symbol":"AC015818.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20526102,"end":20526210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204644.9","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672392,"end":29681110,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000204323.5","gene_symbol":"SMIM5","gene_name":"small integral membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:40030]","synonyms":"C17orf109","biotype":"protein_coding","ncbi_id":"643008","summary":null,"start":75633434,"end":75641404,"strand":1,"description":"small integral membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:40030]"}, {"versioned_ensembl_gene_id":"ENSG00000122176.10","gene_symbol":"FMOD","gene_name":"fibromodulin [Source:HGNC Symbol;Acc:HGNC:3774]","synonyms":"SLRR2E","biotype":"protein_coding","ncbi_id":"2331","summary":"Fibromodulin belongs to the family of small interstitial proteoglycans. The encoded protein possesses a central region containing leucine-rich repeats with 4 keratan sulfate chains, flanked by terminal domains containing disulphide bonds. Owing to the interaction with type I and type II collagen fibrils and in vitro inhibition of fibrillogenesis, the encoded protein may play a role in the assembly of extracellular matrix. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix. Sequence variations in this gene may be associated with the pathogenesis of high myopia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":203340628,"end":203351489,"strand":-1,"description":"fibromodulin [Source:HGNC Symbol;Acc:HGNC:3774]"}, {"versioned_ensembl_gene_id":"ENSG00000236523.2","gene_symbol":"NPM1P40","gene_name":"nucleophosmin 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:45219]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289584","summary":null,"start":203255743,"end":203256475,"strand":1,"description":"nucleophosmin 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:45219]"}, {"versioned_ensembl_gene_id":"ENSG00000188011.5","gene_symbol":"RTP5","gene_name":"receptor transporter protein 5 (putative) [Source:HGNC Symbol;Acc:HGNC:26585]","synonyms":"FLJ33590,CXXC11,C2orf85,Z3CXXC5","biotype":"protein_coding","ncbi_id":"285093","summary":null,"start":241869600,"end":241873823,"strand":1,"description":"receptor transporter protein 5 (putative) [Source:HGNC Symbol;Acc:HGNC:26585]"}, {"versioned_ensembl_gene_id":"ENSG00000249085.1","gene_symbol":"AC035140.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72794405,"end":72816565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083312.17","gene_symbol":"TNPO1","gene_name":"transportin 1 [Source:HGNC Symbol;Acc:HGNC:6401]","synonyms":"IPO2,TRN,MIP1,MIP,KPNB2","biotype":"protein_coding","ncbi_id":"3842","summary":"This gene encodes the beta subunit of the karyopherin receptor complex which interacts with nuclear localization signals to target nuclear proteins to the nucleus. The karyopherin receptor complex is a heterodimer of an alpha subunit which recognizes the nuclear localization signal and a beta subunit which docks the complex at nucleoporins. Alternate splicing of this gene results in several transcript variants encoding different proteins. [provided by RefSeq, Jun 2018]","start":72816312,"end":72916733,"strand":1,"description":"transportin 1 [Source:HGNC Symbol;Acc:HGNC:6401]"}, {"versioned_ensembl_gene_id":"ENSG00000223497.1","gene_symbol":"AC063979.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":72733833,"end":72734209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144580.13","gene_symbol":"CNOT9","gene_name":"CCR4-NOT transcription complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:10445]","synonyms":"RQCD1,RCD1+,RCD1,CT129,CAF40","biotype":"protein_coding","ncbi_id":"9125","summary":"This gene encodes a member of the highly conserved RCD1 protein family. The encoded protein is a transcriptional cofactor and a core protein of the CCR4-NOT complex. It may be involved in signal transduction as well as retinoic acid-regulated cell differentiation and development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2012]","start":218568580,"end":218597080,"strand":1,"description":"CCR4-NOT transcription complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:10445]"}, {"versioned_ensembl_gene_id":"ENSG00000131951.10","gene_symbol":"LRRC9","gene_name":"leucine rich repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:19848]","synonyms":"FLJ46156","biotype":"protein_coding","ncbi_id":"341883","summary":null,"start":59919713,"end":60063559,"strand":1,"description":"leucine rich repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:19848]"}, {"versioned_ensembl_gene_id":"ENSG00000178175.11","gene_symbol":"ZNF366","gene_name":"zinc finger protein 366 [Source:HGNC Symbol;Acc:HGNC:18316]","synonyms":"FLJ39796","biotype":"protein_coding","ncbi_id":"167465","summary":null,"start":72442652,"end":72507727,"strand":-1,"description":"zinc finger protein 366 [Source:HGNC Symbol;Acc:HGNC:18316]"}, {"versioned_ensembl_gene_id":"ENSG00000249362.1","gene_symbol":"LINC02488","gene_name":"long intergenic non-protein coding RNA 2488 [Source:HGNC Symbol;Acc:HGNC:53467]","synonyms":"CTD-2316B1","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87662042,"end":87679147,"strand":1,"description":"long intergenic non-protein coding RNA 2488 [Source:HGNC Symbol;Acc:HGNC:53467]"}, {"versioned_ensembl_gene_id":"ENSG00000281881.1","gene_symbol":"SPRY4-IT1","gene_name":"SPRY4 intronic transcript 1 [Source:NCBI gene;Acc:100642175]","synonyms":"SPRIGHTLY","biotype":"lincRNA","ncbi_id":"100642175","summary":"This gene produces a non-coding RNA that is upregulated in several different tumors, including melanoma and breast and prostate cancer cells. This transcript may mediate cell growth, proliferation, and apoptosis. It regulates levels of lipin 2, and therefore may be involved in lipid biosynthesis. The primary transcript is cleaved to release a mature product that localizes to the cytoplasm (PMID:25344859). The full length structure of the primary and cleaved transcripts is unclear, and it is possible that the primary transcript is a splice variant of SPRY4 (sprouty RTK signaling antagonist 4). [provided by RefSeq, Feb 2016]","start":142317620,"end":142318322,"strand":-1,"description":"SPRY4 intronic transcript 1 [Source:NCBI gene;Acc:100642175]"}, {"versioned_ensembl_gene_id":"ENSG00000255296.1","gene_symbol":"AP002490.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71938671,"end":71939544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262188.1","gene_symbol":"LINC01978","gene_name":"long intergenic non-protein coding RNA 1978 [Source:HGNC Symbol;Acc:HGNC:52806]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928738","summary":null,"start":79919357,"end":79925462,"strand":1,"description":"long intergenic non-protein coding RNA 1978 [Source:HGNC Symbol;Acc:HGNC:52806]"}, {"versioned_ensembl_gene_id":"ENSG00000262343.1","gene_symbol":"AC100791.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79848058,"end":79850110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132003.9","gene_symbol":"ZSWIM4","gene_name":"zinc finger SWIM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:25704]","synonyms":"FLJ12221","biotype":"protein_coding","ncbi_id":"65249","summary":null,"start":13795460,"end":13832230,"strand":1,"description":"zinc finger SWIM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:25704]"}, {"versioned_ensembl_gene_id":"ENSG00000137522.17","gene_symbol":"RNF121","gene_name":"ring finger protein 121 [Source:HGNC Symbol;Acc:HGNC:21070]","synonyms":"FLJ11099","biotype":"protein_coding","ncbi_id":"55298","summary":"The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Several alternatively spliced transcript variants have been noted for this gene, however, not all are likely to encode viable protein products. [provided by RefSeq, Sep 2008]","start":71928701,"end":71997597,"strand":1,"description":"ring finger protein 121 [Source:HGNC Symbol;Acc:HGNC:21070]"}, {"versioned_ensembl_gene_id":"ENSG00000273340.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29741731,"end":29748969,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000134809.8","gene_symbol":"TIMM10","gene_name":"translocase of inner mitochondrial membrane 10 [Source:HGNC Symbol;Acc:HGNC:11814]","synonyms":"TIMM10A,TIM10A,TIM10","biotype":"protein_coding","ncbi_id":"26519","summary":"The mitochondrial protein encoded by this gene belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane, functioning as intermembrane space chaperones for the highly insoluble carrier proteins. [provided by RefSeq, Nov 2011]","start":57528463,"end":57530803,"strand":-1,"description":"translocase of inner mitochondrial membrane 10 [Source:HGNC Symbol;Acc:HGNC:11814]"}, {"versioned_ensembl_gene_id":"ENSG00000123609.10","gene_symbol":"NMI","gene_name":"N-myc and STAT interactor [Source:HGNC Symbol;Acc:HGNC:7854]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9111","summary":"NMYC interactor (NMI) encodes a protein that interacts with NMYC and CMYC (two members of the oncogene Myc family), and other transcription factors containing a Zip, HLH, or HLH-Zip motif. The NMI protein also interacts with all STATs except STAT2 and augments STAT-mediated transcription in response to cytokines IL2 and IFN-gamma. The NMI mRNA has low expression levels in all human fetal and adult tissues tested except brain and has high expression in cancer cell line-myeloid leukemias. [provided by RefSeq, Jul 2008]","start":151270465,"end":151290057,"strand":-1,"description":"N-myc and STAT interactor [Source:HGNC Symbol;Acc:HGNC:7854]"}, {"versioned_ensembl_gene_id":"ENSG00000214832.5","gene_symbol":"UPF3AP2","gene_name":"UPF3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30567]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"147150","summary":null,"start":20375369,"end":20376840,"strand":-1,"description":"UPF3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30567]"}, {"versioned_ensembl_gene_id":"ENSG00000266839.3","gene_symbol":"AC008088.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":20323058,"end":20323337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216475.1","gene_symbol":"AL024474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144257034,"end":144257624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143493.12","gene_symbol":"INTS7","gene_name":"integrator complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:24484]","synonyms":"INT7,DKFZP434B168,C1orf73","biotype":"protein_coding","ncbi_id":"25896","summary":"This gene encodes a subunit of the integrator complex. The integrator complex associates with the C-terminal domain of RNA polymerase II and mediates 3'-end processing of the small nuclear RNAs U1 and U2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":211940399,"end":212035542,"strand":-1,"description":"integrator complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:24484]"}, {"versioned_ensembl_gene_id":"ENSG00000230325.1","gene_symbol":"AL359921.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":236540094,"end":236550280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236885.1","gene_symbol":"AC018731.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151117955,"end":151186209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112539.14","gene_symbol":"C6orf118","gene_name":"chromosome 6 open reading frame 118 [Source:HGNC Symbol;Acc:HGNC:21233]","synonyms":"MGC23884,bA85G2.1","biotype":"protein_coding","ncbi_id":"168090","summary":null,"start":165279664,"end":165309607,"strand":-1,"description":"chromosome 6 open reading frame 118 [Source:HGNC Symbol;Acc:HGNC:21233]"}, {"versioned_ensembl_gene_id":"ENSG00000129595.12","gene_symbol":"EPB41L4A","gene_name":"erythrocyte membrane protein band 4.1 like 4A [Source:HGNC Symbol;Acc:HGNC:13278]","synonyms":"NBL4","biotype":"protein_coding","ncbi_id":"64097","summary":"The protein encoded by this gene is a member of the band 4.1 protein superfamily. Members of this superfamily are thought to play an important role in regulating interactions between the cytoskeleton and plasma membrane, and contain an amino terminal conserved domain that binds glycophorin C. This gene product is thought to be involved in the beta-catenin signaling pathway. [provided by RefSeq, Dec 2016]","start":112142441,"end":112419316,"strand":-1,"description":"erythrocyte membrane protein band 4.1 like 4A [Source:HGNC Symbol;Acc:HGNC:13278]"}, {"versioned_ensembl_gene_id":"ENSG00000089685.14","gene_symbol":"BIRC5","gene_name":"baculoviral IAP repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:593]","synonyms":"EPR-1,API4,survivin","biotype":"protein_coding","ncbi_id":"332","summary":"This gene is a member of the inhibitor of apoptosis (IAP) gene family, which encode negative regulatory proteins that prevent apoptotic cell death. IAP family members usually contain multiple baculovirus IAP repeat (BIR) domains, but this gene encodes proteins with only a single BIR domain. The encoded proteins also lack a C-terminus RING finger domain. Gene expression is high during fetal development and in most tumors, yet low in adult tissues. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":78214186,"end":78225636,"strand":1,"description":"baculoviral IAP repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:593]"}, {"versioned_ensembl_gene_id":"ENSG00000274756.1","gene_symbol":"AC243732.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36574462,"end":36575325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091513.14","gene_symbol":"TF","gene_name":"transferrin [Source:HGNC Symbol;Acc:HGNC:11740]","synonyms":"PRO2086,PRO1557","biotype":"protein_coding","ncbi_id":"7018","summary":"This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]","start":133745956,"end":133779006,"strand":1,"description":"transferrin [Source:HGNC Symbol;Acc:HGNC:11740]"}, {"versioned_ensembl_gene_id":"ENSG00000168671.9","gene_symbol":"UGT3A2","gene_name":"UDP glycosyltransferase family 3 member A2 [Source:HGNC Symbol;Acc:HGNC:27266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"167127","summary":null,"start":36035017,"end":36071358,"strand":-1,"description":"UDP glycosyltransferase family 3 member A2 [Source:HGNC Symbol;Acc:HGNC:27266]"}, {"versioned_ensembl_gene_id":"ENSG00000090060.17","gene_symbol":"PAPOLA","gene_name":"poly(A) polymerase alpha [Source:HGNC Symbol;Acc:HGNC:14981]","synonyms":"PAP","biotype":"protein_coding","ncbi_id":"10914","summary":"The protein encoded by this gene belongs to the poly(A) polymerase family. It is required for the addition of adenosine residues for the creation of the 3'-poly(A) tail of mRNAs. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":96501433,"end":96567111,"strand":1,"description":"poly(A) polymerase alpha [Source:HGNC Symbol;Acc:HGNC:14981]"}, {"versioned_ensembl_gene_id":"ENSG00000278912.1","gene_symbol":"AC008870.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23696665,"end":23697314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232638.1","gene_symbol":"AL390294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8051541,"end":8053084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258376.2","gene_symbol":"AC004846.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73242651,"end":73245979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276505.1","gene_symbol":"AP000892.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":117297005,"end":117297328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278768.1","gene_symbol":"BACE1-AS","gene_name":"BACE1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:37125]","synonyms":"BACE1-AS1,NCRNA00177,FJ573250,BACE1AS","biotype":"antisense_RNA","ncbi_id":"100379571","summary":"This gene encodes an unspliced long non-coding RNA transcribed from the opposite strand to BACE1. The encoded transcript is thought to form an RNA duplex with BACE1 mRNA thereby regulating its expression and is also thought to promote post-transcriptional feed-forward regulation of BACE1. This may lead to increased levels of beta amyloid and increased senile plaque deposition, and therefore may play a role in the pathophysiology of Alzheimer's disease. [provided by RefSeq, Jan 2015]","start":117290874,"end":117293571,"strand":1,"description":"BACE1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:37125]"}, {"versioned_ensembl_gene_id":"ENSG00000249748.1","gene_symbol":"AC112204.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35938822,"end":35939993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258716.1","gene_symbol":"AL139193.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90697333,"end":90699374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104774.12","gene_symbol":"MAN2B1","gene_name":"mannosidase alpha class 2B member 1 [Source:HGNC Symbol;Acc:HGNC:6826]","synonyms":"MANB,LAMAN","biotype":"protein_coding","ncbi_id":"4125","summary":"This gene encodes an enzyme that hydrolyzes terminal, non-reducing alpha-D-mannose residues in alpha-D-mannosides. Its activity is necessary for the catabolism of N-linked carbohydrates released during glycoprotein turnover and it is member of family 38 of glycosyl hydrolases. The full length protein is processed in two steps. First, a 49 aa leader sequence is cleaved off and the remainder of the protein is processed into 3 peptides of 70 kDa, 42 kDa (D) and 13/15 kDa (E). Next, the 70 kDa peptide is further processed into three peptides (A, B and C). The A, B and C peptides are disulfide-linked. Defects in this gene have been associated with lysosomal alpha-mannosidosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]","start":12646511,"end":12666742,"strand":-1,"description":"mannosidase alpha class 2B member 1 [Source:HGNC Symbol;Acc:HGNC:6826]"}, {"versioned_ensembl_gene_id":"ENSG00000276277.1","gene_symbol":"AL445584.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42213841,"end":42213918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113319.12","gene_symbol":"RASGRF2","gene_name":"Ras protein specific guanine nucleotide releasing factor 2 [Source:HGNC Symbol;Acc:HGNC:9876]","synonyms":"Ras-GRF2,GRF2","biotype":"protein_coding","ncbi_id":"5924","summary":"RAS GTPases cycle between an inactive GDP-bound state and an active GTP-bound state. This gene encodes a calcium-regulated nucleotide exchange factor activating both RAS and RAS-related protein, RAC1, through the exchange of bound GDP for GTP, thereby, coordinating the signaling of distinct mitogen-activated protein kinase pathways. [provided by RefSeq, Oct 2011]","start":80960672,"end":81230156,"strand":1,"description":"Ras protein specific guanine nucleotide releasing factor 2 [Source:HGNC Symbol;Acc:HGNC:9876]"}, {"versioned_ensembl_gene_id":"ENSG00000277357.1","gene_symbol":"NPAP1P7","gene_name":"nuclear pore associated protein 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51473]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107161163","summary":null,"start":87825146,"end":87825968,"strand":1,"description":"nuclear pore associated protein 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51473]"}, {"versioned_ensembl_gene_id":"ENSG00000242477.1","gene_symbol":"AC091429.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86884231,"end":86884881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257012.1","gene_symbol":"AP002383.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95040411,"end":95041571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248701.1","gene_symbol":"AC008539.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86797685,"end":86800280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232220.2","gene_symbol":"AC008440.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53874626,"end":53876049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232324.1","gene_symbol":"AC008440.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53864763,"end":53866140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172318.5","gene_symbol":"B3GALT1","gene_name":"beta-1,3-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:916]","synonyms":"beta3Gal-T1","biotype":"protein_coding","ncbi_id":"8708","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is expressed exclusively in the brain. The encoded protein shows strict donor substrate specificity for UDP-galactose. [provided by RefSeq, Jul 2008]","start":167868948,"end":167874041,"strand":1,"description":"beta-1,3-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:916]"}, {"versioned_ensembl_gene_id":"ENSG00000134824.13","gene_symbol":"FADS2","gene_name":"fatty acid desaturase 2 [Source:HGNC Symbol;Acc:HGNC:3575]","synonyms":"TU13,SLL0262,LLCDL2,FADSD6,DES6,D6D","biotype":"protein_coding","ncbi_id":"9415","summary":"The protein encoded by this gene is a member of the fatty acid desaturase (FADS) gene family. Desaturase enzymes regulate unsaturation of fatty acids through the introduction of double bonds between defined carbons of the fatty acyl chain. FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion, both of which are characterized by conserved histidine motifs. This gene is clustered with family members at 11q12-q13.1; this cluster is thought to have arisen evolutionarily from gene duplication based on its similar exon/intron organization. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":61792980,"end":61867354,"strand":1,"description":"fatty acid desaturase 2 [Source:HGNC Symbol;Acc:HGNC:3575]"}, {"versioned_ensembl_gene_id":"ENSG00000070269.13","gene_symbol":"TMEM260","gene_name":"transmembrane protein 260 [Source:HGNC Symbol;Acc:HGNC:20185]","synonyms":"FLJ20392,C14orf101","biotype":"protein_coding","ncbi_id":"54916","summary":null,"start":56488354,"end":56650606,"strand":1,"description":"transmembrane protein 260 [Source:HGNC Symbol;Acc:HGNC:20185]"}, {"versioned_ensembl_gene_id":"ENSG00000265995.1","gene_symbol":"AC069114.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71890409,"end":71944577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117625.13","gene_symbol":"RCOR3","gene_name":"REST corepressor 3 [Source:HGNC Symbol;Acc:HGNC:25594]","synonyms":"FLJ10876","biotype":"protein_coding","ncbi_id":"55758","summary":null,"start":211258377,"end":211316385,"strand":1,"description":"REST corepressor 3 [Source:HGNC Symbol;Acc:HGNC:25594]"}, {"versioned_ensembl_gene_id":"ENSG00000101347.8","gene_symbol":"SAMHD1","gene_name":"SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:15925]","synonyms":"SBBI88,MOP-5,Mg11,HDDC1,AGS5","biotype":"protein_coding","ncbi_id":"25939","summary":"This gene may play a role in regulation of the innate immune response. The encoded protein is upregulated in response to viral infection and may be involved in mediation of tumor necrosis factor-alpha proinflammatory responses. Mutations in this gene have been associated with Aicardi-Goutieres syndrome. [provided by RefSeq, Mar 2010]","start":36890229,"end":36951843,"strand":-1,"description":"SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:15925]"}, {"versioned_ensembl_gene_id":"ENSG00000236234.1","gene_symbol":"AC091132.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45452844,"end":45464065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249792.1","gene_symbol":"AC117522.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85212958,"end":85213614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280046.1","gene_symbol":"AC104581.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7858943,"end":7866083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214853.5","gene_symbol":"AC113412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84999812,"end":85000315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271649.1","gene_symbol":"LINC00904","gene_name":"long intergenic non-protein coding RNA 904 [Source:HGNC Symbol;Acc:HGNC:44325]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652909","summary":null,"start":34892029,"end":34898943,"strand":-1,"description":"long intergenic non-protein coding RNA 904 [Source:HGNC Symbol;Acc:HGNC:44325]"}, {"versioned_ensembl_gene_id":"ENSG00000267767.2","gene_symbol":"LINC01801","gene_name":"long intergenic non-protein coding RNA 1801 [Source:HGNC Symbol;Acc:HGNC:52592]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400685","summary":null,"start":34788582,"end":34832869,"strand":-1,"description":"long intergenic non-protein coding RNA 1801 [Source:HGNC Symbol;Acc:HGNC:52592]"}, {"versioned_ensembl_gene_id":"ENSG00000213368.3","gene_symbol":"AP002383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94913047,"end":94913766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274724.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724448,"end":54736134,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000254671.2","gene_symbol":"STT3A-AS1","gene_name":"STT3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44585]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105369550","summary":null,"start":125570284,"end":125592568,"strand":-1,"description":"STT3A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44585]"}, {"versioned_ensembl_gene_id":"ENSG00000231256.7","gene_symbol":"C17orf105","gene_name":"chromosome 17 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:37241]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284067","summary":null,"start":43780435,"end":43787612,"strand":1,"description":"chromosome 17 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:37241]"}, {"versioned_ensembl_gene_id":"ENSG00000145888.10","gene_symbol":"GLRA1","gene_name":"glycine receptor alpha 1 [Source:HGNC Symbol;Acc:HGNC:4326]","synonyms":"STHE","biotype":"protein_coding","ncbi_id":"2741","summary":"The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found. [provided by RefSeq, Dec 2015]","start":151822513,"end":151924842,"strand":-1,"description":"glycine receptor alpha 1 [Source:HGNC Symbol;Acc:HGNC:4326]"}, {"versioned_ensembl_gene_id":"ENSG00000236489.1","gene_symbol":"AC133473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185606575,"end":185606873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230530.1","gene_symbol":"LIMD1-AS1","gene_name":"LIMD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44107]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644714","summary":null,"start":45679043,"end":45689134,"strand":-1,"description":"LIMD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44107]"}, {"versioned_ensembl_gene_id":"ENSG00000265746.1","gene_symbol":"KYNUP2","gene_name":"kynureninase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39200]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729310","summary":null,"start":19082437,"end":19084834,"strand":1,"description":"kynureninase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39200]"}, {"versioned_ensembl_gene_id":"ENSG00000211961.3","gene_symbol":"IGHV1-45","gene_name":"immunoglobulin heavy variable 1-45 [Source:HGNC Symbol;Acc:HGNC:5553]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28466","summary":null,"start":106506996,"end":106507491,"strand":-1,"description":"immunoglobulin heavy variable 1-45 [Source:HGNC Symbol;Acc:HGNC:5553]"}, {"versioned_ensembl_gene_id":"ENSG00000141736.13","gene_symbol":"ERBB2","gene_name":"erb-b2 receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:3430]","synonyms":"HER2,HER-2,CD340,NGL,NEU","biotype":"protein_coding","ncbi_id":"2064","summary":"This gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways, such as those involving mitogen-activated protein kinase and phosphatidylinositol-3 kinase. Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported, with the most common allele, Ile654/Ile655, shown here. Amplification and/or overexpression of this gene has been reported in numerous cancers, including breast and ovarian tumors. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized. [provided by RefSeq, Jul 2008]","start":39687914,"end":39730426,"strand":1,"description":"erb-b2 receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:3430]"}, {"versioned_ensembl_gene_id":"ENSG00000280143.1","gene_symbol":"AP000892.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":117204967,"end":117210292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224259.6","gene_symbol":"LINC01133","gene_name":"long intergenic non-protein coding RNA 1133 [Source:HGNC Symbol;Acc:HGNC:49447]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505633","summary":null,"start":159961218,"end":159984750,"strand":1,"description":"long intergenic non-protein coding RNA 1133 [Source:HGNC Symbol;Acc:HGNC:49447]"}, {"versioned_ensembl_gene_id":"ENSG00000239480.1","gene_symbol":"AC073517.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102426818,"end":102434780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160993.3","gene_symbol":"ALKBH4","gene_name":"alkB homolog 4, lysine demethylase [Source:HGNC Symbol;Acc:HGNC:21900]","synonyms":"FLJ20013","biotype":"protein_coding","ncbi_id":"54784","summary":null,"start":102456238,"end":102464876,"strand":-1,"description":"alkB homolog 4, lysine demethylase [Source:HGNC Symbol;Acc:HGNC:21900]"}, {"versioned_ensembl_gene_id":"ENSG00000278805.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814475,"end":54828769,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000149554.12","gene_symbol":"CHEK1","gene_name":"checkpoint kinase 1 [Source:HGNC Symbol;Acc:HGNC:1925]","synonyms":"CHK1","biotype":"protein_coding","ncbi_id":"1111","summary":"The protein encoded by this gene belongs to the Ser/Thr protein kinase family. It is required for checkpoint mediated cell cycle arrest in response to DNA damage or the presence of unreplicated DNA. This protein acts to integrate signals from ATM and ATR, two cell cycle proteins involved in DNA damage responses, that also associate with chromatin in meiotic prophase I. Phosphorylation of CDC25A protein phosphatase by this protein is required for cells to delay cell cycle progression in response to double-strand DNA breaks. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2011]","start":125625136,"end":125676255,"strand":1,"description":"checkpoint kinase 1 [Source:HGNC Symbol;Acc:HGNC:1925]"}, {"versioned_ensembl_gene_id":"ENSG00000279161.1","gene_symbol":"AC093503.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46636810,"end":46639161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256443.1","gene_symbol":"AP003559.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61539516,"end":61542259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172500.12","gene_symbol":"FIBP","gene_name":"FGF1 intracellular binding protein [Source:HGNC Symbol;Acc:HGNC:3705]","synonyms":"FGFIBP","biotype":"protein_coding","ncbi_id":"9158","summary":"Acidic fibroblast growth factor is mitogenic for a variety of different cell types and acts by stimulating mitogenesis or inducing morphological changes and differentiation. The FIBP protein is an intracellular protein that binds selectively to acidic fibroblast growth factor (aFGF). It is postulated that FIBP may be involved in the mitogenic action of aFGF. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":65883741,"end":65888539,"strand":-1,"description":"FGF1 intracellular binding protein [Source:HGNC Symbol;Acc:HGNC:3705]"}, {"versioned_ensembl_gene_id":"ENSG00000239917.3","gene_symbol":"RPS10P16","gene_name":"ribosomal protein S10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36200]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100271050","summary":null,"start":117523271,"end":117524061,"strand":-1,"description":"ribosomal protein S10 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36200]"}, {"versioned_ensembl_gene_id":"ENSG00000267253.1","gene_symbol":"AC055813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43718314,"end":43720436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242931.1","gene_symbol":"RPL7P49","gene_name":"ribosomal protein L7 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36912]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271221","summary":null,"start":76430417,"end":76431124,"strand":-1,"description":"ribosomal protein L7 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:36912]"}, {"versioned_ensembl_gene_id":"ENSG00000251270.1","gene_symbol":"AC108727.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141115124,"end":141124182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234417.1","gene_symbol":"AL662831.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30349077,"end":30349710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213698.2","gene_symbol":"AC240504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72727977,"end":72728821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228862.3","gene_symbol":"AC068389.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60631509,"end":60636271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271119.1","gene_symbol":"AC026412.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1594626,"end":1611467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235961.5","gene_symbol":"PNMA6A","gene_name":"paraneoplastic Ma antigen family member 6A [Source:HGNC Symbol;Acc:HGNC:28248]","synonyms":"PNMA6C,MGC15827","biotype":"protein_coding","ncbi_id":"84968","summary":null,"start":153072482,"end":153075018,"strand":1,"description":"paraneoplastic Ma antigen family member 6A [Source:HGNC Symbol;Acc:HGNC:28248]"}, {"versioned_ensembl_gene_id":"ENSG00000188002.10","gene_symbol":"AC026412.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1598920,"end":1634005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086619.13","gene_symbol":"ERO1B","gene_name":"endoplasmic reticulum oxidoreductase 1 beta [Source:HGNC Symbol;Acc:HGNC:14355]","synonyms":"ERO1LB,Ero1beta,ERO1-L(beta)","biotype":"protein_coding","ncbi_id":"56605","summary":null,"start":236215555,"end":236281985,"strand":-1,"description":"endoplasmic reticulum oxidoreductase 1 beta [Source:HGNC Symbol;Acc:HGNC:14355]"}, {"versioned_ensembl_gene_id":"ENSG00000266642.2","gene_symbol":"AC024267.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28897738,"end":28899402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167536.13","gene_symbol":"DHRS13","gene_name":"dehydrogenase/reductase 13 [Source:HGNC Symbol;Acc:HGNC:28326]","synonyms":"SDR7C5,MGC23280","biotype":"protein_coding","ncbi_id":"147015","summary":null,"start":28897781,"end":28903071,"strand":-1,"description":"dehydrogenase/reductase 13 [Source:HGNC Symbol;Acc:HGNC:28326]"}, {"versioned_ensembl_gene_id":"ENSG00000164403.14","gene_symbol":"SHROOM1","gene_name":"shroom family member 1 [Source:HGNC Symbol;Acc:HGNC:24084]","synonyms":"KIAA1960,APXL2","biotype":"protein_coding","ncbi_id":"134549","summary":"SHROOM family members play diverse roles in the development of the nervous system and other tissues (Hagens et al., 2006 [PubMed 16615870]).[supplied by OMIM, Mar 2008]","start":132822141,"end":132830898,"strand":-1,"description":"shroom family member 1 [Source:HGNC Symbol;Acc:HGNC:24084]"}, {"versioned_ensembl_gene_id":"ENSG00000225300.1","gene_symbol":"AL591623.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":246605873,"end":246608102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228955.2","gene_symbol":"AL591623.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":246632251,"end":246632478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179071.4","gene_symbol":"CCDC89","gene_name":"coiled-coil domain containing 89 [Source:HGNC Symbol;Acc:HGNC:26762]","synonyms":"FLJ38159","biotype":"protein_coding","ncbi_id":"220388","summary":null,"start":85684866,"end":85686277,"strand":-1,"description":"coiled-coil domain containing 89 [Source:HGNC Symbol;Acc:HGNC:26762]"}, {"versioned_ensembl_gene_id":"ENSG00000151292.17","gene_symbol":"CSNK1G3","gene_name":"casein kinase 1 gamma 3 [Source:HGNC Symbol;Acc:HGNC:2456]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1456","summary":"This gene encodes a member of a family of serine/threonine protein kinases that phosphorylate caseins and other acidic proteins. A related protein in the African clawed frog participates in the transmission of Wnt/beta-catenin signaling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":123512099,"end":123617045,"strand":1,"description":"casein kinase 1 gamma 3 [Source:HGNC Symbol;Acc:HGNC:2456]"}, {"versioned_ensembl_gene_id":"ENSG00000224887.1","gene_symbol":"AL513318.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87084161,"end":87085151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134817.10","gene_symbol":"APLNR","gene_name":"apelin receptor [Source:HGNC Symbol;Acc:HGNC:339]","synonyms":"FLJ90771,APJR,APJ,AGTRL1","biotype":"protein_coding","ncbi_id":"187","summary":"This gene encodes a member of the G protein-coupled receptor gene family. The encoded protein is related to the angiotensin receptor, but is actually an apelin receptor that inhibits adenylate cyclase activity and plays a counter-regulatory role against the pressure action of angiotensin II by exerting hypertensive effect. It functions in the cardiovascular and central nervous systems, in glucose metabolism, in embryonic and tumor angiogenesis and as a human immunodeficiency virus (HIV-1) coreceptor. Two transcript variants resulting from alternative splicing have been identified. [provided by RefSeq, Jul 2009]","start":57233577,"end":57237314,"strand":-1,"description":"apelin receptor [Source:HGNC Symbol;Acc:HGNC:339]"}, {"versioned_ensembl_gene_id":"ENSG00000226237.1","gene_symbol":"GAS1RR","gene_name":"GAS1 adjacent regulatory RNA [Source:HGNC Symbol;Acc:HGNC:52261]","synonyms":"LncRNA-Hh","biotype":"lincRNA","ncbi_id":"100506834","summary":null,"start":86948699,"end":87002033,"strand":1,"description":"GAS1 adjacent regulatory RNA [Source:HGNC Symbol;Acc:HGNC:52261]"}, {"versioned_ensembl_gene_id":"ENSG00000269354.1","gene_symbol":"AC243960.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41639659,"end":41640602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260670.1","gene_symbol":"AC134508.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72321051,"end":72324027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279694.1","gene_symbol":"AC011270.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78339208,"end":78341757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232211.1","gene_symbol":"AL353613.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86632147,"end":86696496,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000028839.9","gene_symbol":"TBPL1","gene_name":"TATA-box binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:11589]","synonyms":"TRF2,TLP,TLF,STUD","biotype":"protein_coding","ncbi_id":"9519","summary":"This gene encodes a member of the TATA box-binding protein family. TATA box-binding proteins play a critical role in transcription by RNA polymerase II as components of the transcription factor IID (TFIID) complex. The encoded protein does not bind to the TATA box and initiates transcription from TATA-less promoters. This gene plays a critical role in spermatogenesis, and single nucleotide polymorphisms in this gene may be associated with male infertility. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Nov 2011]","start":133952170,"end":133990432,"strand":1,"description":"TATA-box binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:11589]"}, {"versioned_ensembl_gene_id":"ENSG00000273255.1","gene_symbol":"AP001521.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57055587,"end":57056132,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241163.7","gene_symbol":"LINC00877","gene_name":"long intergenic non-protein coding RNA 877 [Source:HGNC Symbol;Acc:HGNC:27706]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285286","summary":null,"start":72035300,"end":72279503,"strand":-1,"description":"long intergenic non-protein coding RNA 877 [Source:HGNC Symbol;Acc:HGNC:27706]"}, {"versioned_ensembl_gene_id":"ENSG00000242609.1","gene_symbol":"AC105265.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72086888,"end":72087725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000020922.12","gene_symbol":"MRE11","gene_name":"MRE11 homolog, double strand break repair nuclease [Source:HGNC Symbol;Acc:HGNC:7230]","synonyms":"MRE11A,ATLD","biotype":"protein_coding","ncbi_id":"4361","summary":"This gene encodes a nuclear protein involved in homologous recombination, telomere length maintenance, and DNA double-strand break repair. By itself, the protein has 3' to 5' exonuclease activity and endonuclease activity. The protein forms a complex with the RAD50 homolog; this complex is required for nonhomologous joining of DNA ends and possesses increased single-stranded DNA endonuclease and 3' to 5' exonuclease activities. In conjunction with a DNA ligase, this protein promotes the joining of noncomplementary ends in vitro using short homologies near the ends of the DNA fragments. This gene has a pseudogene on chromosome 3. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":94415578,"end":94493908,"strand":-1,"description":"MRE11 homolog, double strand break repair nuclease [Source:HGNC Symbol;Acc:HGNC:7230]"}, {"versioned_ensembl_gene_id":"ENSG00000134369.15","gene_symbol":"NAV1","gene_name":"neuron navigator 1 [Source:HGNC Symbol;Acc:HGNC:15989]","synonyms":"FLJ12560,DKFZp781D0314,steerin-1,POMFIL3,MGC14961,KIAA1151,FLJ14203","biotype":"protein_coding","ncbi_id":"89796","summary":"This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. The exact function of this gene is not known, but it is thought to play a role in in neuronal development and regeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":201622885,"end":201826969,"strand":1,"description":"neuron navigator 1 [Source:HGNC Symbol;Acc:HGNC:15989]"}, {"versioned_ensembl_gene_id":"ENSG00000253989.2","gene_symbol":"IGHVIII-38-1","gene_name":"immunoglobulin heavy variable (III)-38-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5699]","synonyms":"IGHV(III)-38-1","biotype":"IG_V_pseudogene","ncbi_id":"28346","summary":null,"start":106418018,"end":106418299,"strand":-1,"description":"immunoglobulin heavy variable (III)-38-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5699]"}, {"versioned_ensembl_gene_id":"ENSG00000211958.2","gene_symbol":"IGHV3-38","gene_name":"immunoglobulin heavy variable 3-38 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5601]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28429","summary":null,"start":106410493,"end":106411021,"strand":-1,"description":"immunoglobulin heavy variable 3-38 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5601]"}, {"versioned_ensembl_gene_id":"ENSG00000198168.8","gene_symbol":"SVIP","gene_name":"small VCP interacting protein [Source:HGNC Symbol;Acc:HGNC:25238]","synonyms":"DKFZp313A2432","biotype":"protein_coding","ncbi_id":"258010","summary":"Endoplasmic reticulum-associated degradation (ERAD) is the pathway by which misfolded proteins in the endoplasmic reticulum are targeted to the proteasome for degradation. Multiple specialized proteins interact with one another during ERAD to complete this process. The protein encoded by this gene is an inhibitor of ERAD, functioning to disrupt the interaction of these protein components. This downregulation of ERAD may be needed to protect the cell from overactive protein degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":22813799,"end":22830299,"strand":-1,"description":"small VCP interacting protein [Source:HGNC Symbol;Acc:HGNC:25238]"}, {"versioned_ensembl_gene_id":"ENSG00000230510.6","gene_symbol":"PPP5D1","gene_name":"PPP5 tetratricopeptide repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44209]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506012","summary":null,"start":46480796,"end":46601200,"strand":-1,"description":"PPP5 tetratricopeptide repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44209]"}, {"versioned_ensembl_gene_id":"ENSG00000249035.6","gene_symbol":"CLMAT3","gene_name":"colorectal liver metastasis associated transcript 3 [Source:HGNC Symbol;Acc:HGNC:52287]","synonyms":"SPARC-AS1","biotype":"antisense_RNA","ncbi_id":"101927096","summary":null,"start":151676945,"end":151724782,"strand":1,"description":"colorectal liver metastasis associated transcript 3 [Source:HGNC Symbol;Acc:HGNC:52287]"}, {"versioned_ensembl_gene_id":"ENSG00000075568.16","gene_symbol":"TMEM131","gene_name":"transmembrane protein 131 [Source:HGNC Symbol;Acc:HGNC:30366]","synonyms":"YR-23,RW1,PRO1048,KIAA0257,CC28","biotype":"protein_coding","ncbi_id":"23505","summary":null,"start":97756333,"end":97995891,"strand":-1,"description":"transmembrane protein 131 [Source:HGNC Symbol;Acc:HGNC:30366]"}, {"versioned_ensembl_gene_id":"ENSG00000258546.1","gene_symbol":"CENPUP2","gene_name":"centromere protein U pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49890]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419930","summary":null,"start":25092715,"end":25093900,"strand":-1,"description":"centromere protein U pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49890]"}, {"versioned_ensembl_gene_id":"ENSG00000265800.1","gene_symbol":"AC022211.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75138416,"end":75141350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269179.1","gene_symbol":"AC011452.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49909501,"end":49958391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160789.19","gene_symbol":"LMNA","gene_name":"lamin A/C [Source:HGNC Symbol;Acc:HGNC:6636]","synonyms":"LMN1,LGMD1B,HGPS,CMD1A,PRO1,MADA,LMNL1","biotype":"protein_coding","ncbi_id":"4000","summary":"The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, Apr 2012]","start":156082573,"end":156140089,"strand":1,"description":"lamin A/C [Source:HGNC Symbol;Acc:HGNC:6636]"}, {"versioned_ensembl_gene_id":"ENSG00000137713.15","gene_symbol":"PPP2R1B","gene_name":"protein phosphatase 2 scaffold subunit Abeta [Source:HGNC Symbol;Acc:HGNC:9303]","synonyms":"PR65B,PP2A-Abeta","biotype":"protein_coding","ncbi_id":"5519","summary":"This gene encodes a constant regulatory subunit of protein phosphatase 2. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The constant regulatory subunit A serves as a scaffolding molecule to coordinate the assembly of the catalytic subunit and a variable regulatory B subunit. This gene encodes a beta isoform of the constant regulatory subunit A. Mutations in this gene have been associated with some lung and colon cancers. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":111726908,"end":111766427,"strand":-1,"description":"protein phosphatase 2 scaffold subunit Abeta [Source:HGNC Symbol;Acc:HGNC:9303]"}, {"versioned_ensembl_gene_id":"ENSG00000279971.1","gene_symbol":"AC020910.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34645380,"end":34646838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268729.1","gene_symbol":"AC020922.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55312029,"end":55312495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181296.3","gene_symbol":"OR5G1P","gene_name":"olfactory receptor family 5 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8344]","synonyms":"OR93,OR5G2P,OR11-104","biotype":"unprocessed_pseudogene","ncbi_id":"8591","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56775261,"end":56776206,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8344]"}, {"versioned_ensembl_gene_id":"ENSG00000268751.1","gene_symbol":"SCGB1B2P","gene_name":"secretoglobin family 1B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:20741]","synonyms":"SCGB4A1P","biotype":"lincRNA","ncbi_id":"643719","summary":null,"start":34576733,"end":34577701,"strand":-1,"description":"secretoglobin family 1B member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:20741]"}, {"versioned_ensembl_gene_id":"ENSG00000104388.14","gene_symbol":"RAB2A","gene_name":"RAB2A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9763]","synonyms":"RAB2","biotype":"protein_coding","ncbi_id":"5862","summary":"The protein encoded by this gene belongs to the Rab family, members of which are small molecular weight guanosine triphosphatases (GTPases) that contain highly conserved domains involved in GTP binding and hydrolysis. The Rabs are membrane-bound proteins, involved in vesicular fusion and trafficking. This protein is a resident of pre-Golgi intermediates, and is required for protein transport from the endoplasmic reticulum (ER) to the Golgi complex. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":60516857,"end":60623627,"strand":1,"description":"RAB2A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9763]"}, {"versioned_ensembl_gene_id":"ENSG00000236480.1","gene_symbol":"PKMP1","gene_name":"pyruvate kinase, muscle pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643586","summary":null,"start":114535995,"end":114537840,"strand":1,"description":"pyruvate kinase, muscle pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44243]"}, {"versioned_ensembl_gene_id":"ENSG00000152495.10","gene_symbol":"CAMK4","gene_name":"calcium/calmodulin dependent protein kinase IV [Source:HGNC Symbol;Acc:HGNC:1464]","synonyms":"CaMK-GR","biotype":"protein_coding","ncbi_id":"814","summary":"The product of this gene belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. This enzyme is a multifunctional serine/threonine protein kinase with limited tissue distribution, that has been implicated in transcriptional regulation in lymphocytes, neurons and male germ cells. [provided by RefSeq, Jul 2008]","start":111223653,"end":111494886,"strand":1,"description":"calcium/calmodulin dependent protein kinase IV [Source:HGNC Symbol;Acc:HGNC:1464]"}, {"versioned_ensembl_gene_id":"ENSG00000007129.17","gene_symbol":"CEACAM21","gene_name":"carcinoembryonic antigen related cell adhesion molecule 21 [Source:HGNC Symbol;Acc:HGNC:28834]","synonyms":"R29124_1,FLJ13540","biotype":"protein_coding","ncbi_id":"90273","summary":null,"start":41549518,"end":41586844,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 21 [Source:HGNC Symbol;Acc:HGNC:28834]"}, {"versioned_ensembl_gene_id":"ENSG00000154016.13","gene_symbol":"GRAP","gene_name":"GRB2-related adaptor protein [Source:HGNC Symbol;Acc:HGNC:4562]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10750","summary":"This gene encodes a member of the GRB2/Sem5/Drk family and functions as a cytoplasmic signaling protein which contains an SH2 domain flanked by two SH3 domains. The SH2 domain interacts with ligand-activated receptors for stem cell factor and erythropoietin, and facilitates the formation of a stable complex with the BCR-ABL oncoprotein. This protein also associates with the Ras guanine nucleotide exchange factor SOS1 (son of sevenless homolog 1) through its N-terminal SH3 domain. In general, it couples signals from receptor and cytoplasmic tyrosine kinases to the Ras signaling pathway. [provided by RefSeq, Jul 2012]","start":19020673,"end":19047637,"strand":-1,"description":"GRB2-related adaptor protein [Source:HGNC Symbol;Acc:HGNC:4562]"}, {"versioned_ensembl_gene_id":"ENSG00000248290.1","gene_symbol":"TNXA","gene_name":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]","synonyms":"TNX,HXBL,D6S103E,XA","biotype":"unprocessed_pseudogene","ncbi_id":"7146","summary":null,"start":32008614,"end":32012472,"strand":-1,"description":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]"}, {"versioned_ensembl_gene_id":"ENSG00000267342.1","gene_symbol":"AC087289.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75897060,"end":75900148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163946.13","gene_symbol":"FAM208A","gene_name":"family with sequence similarity 208 member A [Source:HGNC Symbol;Acc:HGNC:30314]","synonyms":"TASOR,se89-1,RAP140,KIAA1105,C3orf63","biotype":"protein_coding","ncbi_id":"23272","summary":null,"start":56620133,"end":56683237,"strand":-1,"description":"family with sequence similarity 208 member A [Source:HGNC Symbol;Acc:HGNC:30314]"}, {"versioned_ensembl_gene_id":"ENSG00000254915.1","gene_symbol":"AP003168.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75942129,"end":75942435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267426.5","gene_symbol":"AC087289.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":75898645,"end":75930129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088280.18","gene_symbol":"ASAP3","gene_name":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:14987]","synonyms":"UPLC1,FLJ20199,DDEFL1,CENTB6","biotype":"protein_coding","ncbi_id":"55616","summary":"This gene encodes a member of a subfamily of ADP-ribosylation factor(Arf) GTPase-activating proteins that contain additional ankyrin repeat and pleckstrin homology domains. The Arf GAP domain of this protein catalyzes the hydrolysis of GTP bound to Arf proteins. The encoded protein promotes cell differentiation and migration and has been implicated in cancer cell invasion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":23428563,"end":23484568,"strand":-1,"description":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:14987]"}, {"versioned_ensembl_gene_id":"ENSG00000204428.12","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31676684,"end":31684040,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000254361.1","gene_symbol":"AC046195.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137852327,"end":137929044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253288.1","gene_symbol":"AC046195.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137809444,"end":138083570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253988.1","gene_symbol":"AC079015.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138063268,"end":138073240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225650.2","gene_symbol":"EIF2S2P5","gene_name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37793]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347675","summary":null,"start":114468315,"end":114469282,"strand":1,"description":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37793]"}, {"versioned_ensembl_gene_id":"ENSG00000260751.2","gene_symbol":"AC008870.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":23568673,"end":23569696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153107.11","gene_symbol":"ANAPC1","gene_name":"anaphase promoting complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:19988]","synonyms":"TSG24,MCPR,APC1","biotype":"protein_coding","ncbi_id":"64682","summary":"This gene encodes a subunit of the anaphase-promoting complex. This complex is an E3 ubiquitin ligase that regulates progression through the metaphase to anaphase portion of the cell cycle by ubiquitinating proteins which targets them for degradation. [provided by RefSeq, Dec 2011]","start":111766271,"end":111884690,"strand":-1,"description":"anaphase promoting complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:19988]"}, {"versioned_ensembl_gene_id":"ENSG00000120049.18","gene_symbol":"KCNIP2","gene_name":"potassium voltage-gated channel interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:15522]","synonyms":"KCHIP2","biotype":"protein_coding","ncbi_id":"30819","summary":"This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belongs to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have EF-hand-like domains, and differ from each other in the N-terminus. They are integral subunit components of native Kv4 channel complexes. They may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified from this gene. [provided by RefSeq, Jul 2008]","start":101825974,"end":101843920,"strand":-1,"description":"potassium voltage-gated channel interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:15522]"}, {"versioned_ensembl_gene_id":"ENSG00000132589.15","gene_symbol":"FLOT2","gene_name":"flotillin 2 [Source:HGNC Symbol;Acc:HGNC:3758]","synonyms":"M17S1,ESA1,ESA,ECS1,ECS-1","biotype":"protein_coding","ncbi_id":"2319","summary":"Caveolae are small domains on the inner cell membrane involved in vesicular trafficking and signal transduction. This gene encodes a caveolae-associated, integral membrane protein, which is thought to function in neuronal signaling. [provided by RefSeq, Jul 2008]","start":28879335,"end":28897679,"strand":-1,"description":"flotillin 2 [Source:HGNC Symbol;Acc:HGNC:3758]"}, {"versioned_ensembl_gene_id":"ENSG00000132471.11","gene_symbol":"WBP2","gene_name":"WW domain binding protein 2 [Source:HGNC Symbol;Acc:HGNC:12738]","synonyms":"WBP-2,GRAMD6","biotype":"protein_coding","ncbi_id":"23558","summary":"The globular WW domain is composed of 38 to 40 semiconserved amino acids shared by proteins of diverse functions including structural, regulatory, and signaling proteins. The domain is involved in mediating protein-protein interactions through the binding of polyproline ligands. This gene encodes a WW domain binding protein that is a transcriptional coactivator of estrogen receptor alpha and progesterone receptor. Defects in this gene have been associated with hearing impairment. [provided by RefSeq, Jan 2017]","start":75845699,"end":75856507,"strand":-1,"description":"WW domain binding protein 2 [Source:HGNC Symbol;Acc:HGNC:12738]"}, {"versioned_ensembl_gene_id":"ENSG00000198753.11","gene_symbol":"PLXNB3","gene_name":"plexin B3 [Source:HGNC Symbol;Acc:HGNC:9105]","synonyms":"PLXN6,PLEXR,PLEXB3","biotype":"protein_coding","ncbi_id":"5365","summary":"The protein encoded by this gene is a member of the plexin family. It functions as a receptor for semaphorin 5A, and plays a role in axon guidance, invasive growth and cell migration. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":153764196,"end":153779346,"strand":1,"description":"plexin B3 [Source:HGNC Symbol;Acc:HGNC:9105]"}, {"versioned_ensembl_gene_id":"ENSG00000255741.1","gene_symbol":"AP000808.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68941503,"end":68942852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263325.1","gene_symbol":"AC003965.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2857898,"end":2859726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211949.3","gene_symbol":"IGHV3-23","gene_name":"immunoglobulin heavy variable 3-23 [Source:HGNC Symbol;Acc:HGNC:5588]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28442","summary":"IGHV3-23 belongs to a cluster of approximately 40 functional variable (V) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the V gene cluster, see (MIM 147070).[supplied by OMIM, Apr 2008]","start":106268606,"end":106269140,"strand":-1,"description":"immunoglobulin heavy variable 3-23 [Source:HGNC Symbol;Acc:HGNC:5588]"}, {"versioned_ensembl_gene_id":"ENSG00000253345.1","gene_symbol":"IGHVII-22-1","gene_name":"immunoglobulin heavy variable (II)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5673]","synonyms":"IGHV(II)-22-1","biotype":"IG_V_pseudogene","ncbi_id":"28374","summary":null,"start":106263362,"end":106263626,"strand":-1,"description":"immunoglobulin heavy variable (II)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5673]"}, {"versioned_ensembl_gene_id":"ENSG00000232902.1","gene_symbol":"BX000531.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497383,"end":29510429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123473.15","gene_symbol":"STIL","gene_name":"STIL, centriolar assembly protein [Source:HGNC Symbol;Acc:HGNC:10879]","synonyms":"SIL,MCPH7","biotype":"protein_coding","ncbi_id":"6491","summary":"This gene encodes a cytoplasmic protein implicated in regulation of the mitotic spindle checkpoint, a regulatory pathway that monitors chromosome segregation during cell division to ensure the proper distribution of chromosomes to daughter cells. The protein is phosphorylated in mitosis and in response to activation of the spindle checkpoint, and disappears when cells transition to G1 phase. It interacts with a mitotic regulator, and its expression is required to efficiently activate the spindle checkpoint. It is proposed to regulate Cdc2 kinase activity during spindle checkpoint arrest. Chromosomal deletions that fuse this gene and the adjacent locus commonly occur in T cell leukemias, and are thought to arise through illegitimate V-(D)-J recombination events. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47250139,"end":47314147,"strand":-1,"description":"STIL, centriolar assembly protein [Source:HGNC Symbol;Acc:HGNC:10879]"}, {"versioned_ensembl_gene_id":"ENSG00000154511.11","gene_symbol":"FAM69A","gene_name":"family with sequence similarity 69 member A [Source:HGNC Symbol;Acc:HGNC:32213]","synonyms":"FLJ23493","biotype":"protein_coding","ncbi_id":"388650","summary":"This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":92832737,"end":92961522,"strand":-1,"description":"family with sequence similarity 69 member A [Source:HGNC Symbol;Acc:HGNC:32213]"}, {"versioned_ensembl_gene_id":"ENSG00000237197.1","gene_symbol":"IGHD1-7","gene_name":"immunoglobulin heavy diversity 1-7 [Source:HGNC Symbol;Acc:HGNC:5486]","synonyms":"IGHD17,DM1","biotype":"IG_D_gene","ncbi_id":"28509","summary":null,"start":105909907,"end":105909923,"strand":-1,"description":"immunoglobulin heavy diversity 1-7 [Source:HGNC Symbol;Acc:HGNC:5486]"}, {"versioned_ensembl_gene_id":"ENSG00000233727.1","gene_symbol":"AL162389.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107853783,"end":107854258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253998.3","gene_symbol":"IGKV2-29","gene_name":"immunoglobulin kappa variable 2-29 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5784]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28920","summary":null,"start":89234174,"end":89234912,"strand":-1,"description":"immunoglobulin kappa variable 2-29 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5784]"}, {"versioned_ensembl_gene_id":"ENSG00000253731.2","gene_symbol":"PCDHGA6","gene_name":"protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:HGNC:8704]","synonyms":"PCDH-GAMMA-A6","biotype":"protein_coding","ncbi_id":"56109","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141373914,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:HGNC:8704]"}, {"versioned_ensembl_gene_id":"ENSG00000235638.1","gene_symbol":"MTND6P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39477]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478948","summary":null,"start":235537520,"end":235538041,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39477]"}, {"versioned_ensembl_gene_id":"ENSG00000215006.4","gene_symbol":"CHCHD2P2","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39586]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728324","summary":null,"start":69333929,"end":69334249,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39586]"}, {"versioned_ensembl_gene_id":"ENSG00000248714.6","gene_symbol":"AC091180.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49361165,"end":49369998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188676.13","gene_symbol":"IDO2","gene_name":"indoleamine 2,3-dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:27269]","synonyms":"INDOL1","biotype":"protein_coding","ncbi_id":"169355","summary":"Along with the enzymes encoded by the INDO (MIM 147435) and TDO2 (MIM 191070) genes, the enzyme encoded by the INDOL1 gene metabolizes tryptophan in the kynurenine pathway (Ball et al., 2007 [PubMed 17499941]).[supplied by OMIM, Feb 2011]","start":39934614,"end":40016391,"strand":1,"description":"indoleamine 2,3-dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:27269]"}, {"versioned_ensembl_gene_id":"ENSG00000253790.1","gene_symbol":"AC007991.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39997869,"end":39998499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187714.6","gene_symbol":"SLC18A3","gene_name":"solute carrier family 18 member A3 [Source:HGNC Symbol;Acc:HGNC:10936]","synonyms":"VACHT","biotype":"protein_coding","ncbi_id":"6572","summary":"This gene is a member of the vesicular amine transporter family. The encoded transmembrane protein transports acetylcholine into secretory vesicles for release into the extracellular space. Acetylcholine transport utilizes a proton gradient established by a vacuolar ATPase. This gene is located within the first intron of the choline acetyltransferase gene. [provided by RefSeq, Jul 2008]","start":49610301,"end":49612720,"strand":1,"description":"solute carrier family 18 member A3 [Source:HGNC Symbol;Acc:HGNC:10936]"}, {"versioned_ensembl_gene_id":"ENSG00000254245.2","gene_symbol":"PCDHGA3","gene_name":"protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:HGNC:8701]","synonyms":"PCDH-GAMMA-A3","biotype":"protein_coding","ncbi_id":"56112","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141343829,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:HGNC:8701]"}, {"versioned_ensembl_gene_id":"ENSG00000259820.1","gene_symbol":"AC083843.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134792020,"end":134798272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163098.4","gene_symbol":"BIRC8","gene_name":"baculoviral IAP repeat containing 8 [Source:HGNC Symbol;Acc:HGNC:14878]","synonyms":"hILP2,ILP-2","biotype":"protein_coding","ncbi_id":"112401","summary":null,"start":53289601,"end":53291626,"strand":-1,"description":"baculoviral IAP repeat containing 8 [Source:HGNC Symbol;Acc:HGNC:14878]"}, {"versioned_ensembl_gene_id":"ENSG00000273947.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2,nkat2a,nkat2b,p58,CD158B2,cl-6","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738538,"end":54753053,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000213934.6","gene_symbol":"HBG1","gene_name":"hemoglobin subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:4831]","synonyms":"HBG-T2","biotype":"protein_coding","ncbi_id":"3047","summary":"The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some beta-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]","start":5248083,"end":5249892,"strand":-1,"description":"hemoglobin subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:4831]"}, {"versioned_ensembl_gene_id":"ENSG00000265817.2","gene_symbol":"FSBP","gene_name":"fibrinogen silencer binding protein [Source:HGNC Symbol;Acc:HGNC:43653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100861412","summary":null,"start":94372170,"end":94436952,"strand":-1,"description":"fibrinogen silencer binding protein [Source:HGNC Symbol;Acc:HGNC:43653]"}, {"versioned_ensembl_gene_id":"ENSG00000252413.1","gene_symbol":"RNU7-121P","gene_name":"RNA, U7 small nuclear 121 pseudogene [Source:HGNC Symbol;Acc:HGNC:45655]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480449","summary":null,"start":39723566,"end":39723627,"strand":-1,"description":"RNA, U7 small nuclear 121 pseudogene [Source:HGNC Symbol;Acc:HGNC:45655]"}, {"versioned_ensembl_gene_id":"ENSG00000278497.1","gene_symbol":"RN7SL759P","gene_name":"RNA, 7SL, cytoplasmic 759, pseudogene [Source:HGNC Symbol;Acc:HGNC:46775]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479498","summary":null,"start":20570886,"end":20571175,"strand":1,"description":"RNA, 7SL, cytoplasmic 759, pseudogene [Source:HGNC Symbol;Acc:HGNC:46775]"}, {"versioned_ensembl_gene_id":"ENSG00000104827.12","gene_symbol":"CGB3","gene_name":"chorionic gonadotropin beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:1886]","synonyms":"CGB","biotype":"protein_coding","ncbi_id":"1082","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 3 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]","start":49022869,"end":49024333,"strand":-1,"description":"chorionic gonadotropin beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:1886]"}, {"versioned_ensembl_gene_id":"ENSG00000267631.4","gene_symbol":"CGB1","gene_name":"chorionic gonadotropin beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:16721]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114335","summary":"The beta subunit of chorionic gonadotropin (CGB) is encoded by six highly homologous and structurally similar genes that are arranged in tandem and inverted pairs on chromosome 19q13.3, and contiguous with the luteinizing hormone beta (LHB) subunit gene. The CGB genes are primarily distinguished by differences in the 5' untranscribed region. This gene was originally thought to be one of the two pseudogenes (CGB1 and CGB2) of CGB subunit, however, detection of CGB1 and CGB2 transcripts in vivo, and their presence on the polysomes, suggested that these transcripts are translated. To date, a protein product corresponding to CGB1 has not been isolated. The deduced sequence of the hypothetical protein of 132 aa does not share any similarity with that of functional CGB subunits (PMID:8954017). However, a 155 aa protein, translated from a different frame, is about the same size, and shares 98% identity with other CGB subunits. [provided by RefSeq, Jul 2008]","start":49035610,"end":49036895,"strand":-1,"description":"chorionic gonadotropin beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:16721]"}, {"versioned_ensembl_gene_id":"ENSG00000279488.1","gene_symbol":"AC004623.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1372238,"end":1374364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278936.1","gene_symbol":"AC244517.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141183401,"end":141201396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265342.1","gene_symbol":"AC011933.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75394123,"end":75394963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120324.8","gene_symbol":"PCDHB10","gene_name":"protocadherin beta 10 [Source:HGNC Symbol;Acc:HGNC:8681]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56126","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141192353,"end":141195642,"strand":1,"description":"protocadherin beta 10 [Source:HGNC Symbol;Acc:HGNC:8681]"}, {"versioned_ensembl_gene_id":"ENSG00000176222.8","gene_symbol":"ZNF404","gene_name":"zinc finger protein 404 [Source:HGNC Symbol;Acc:HGNC:19417]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342908","summary":null,"start":43872363,"end":43901385,"strand":-1,"description":"zinc finger protein 404 [Source:HGNC Symbol;Acc:HGNC:19417]"}, {"versioned_ensembl_gene_id":"ENSG00000160953.15","gene_symbol":"MUM1","gene_name":"melanoma associated antigen (mutated) 1 [Source:HGNC Symbol;Acc:HGNC:29641]","synonyms":"MUM-1,EXPAND1","biotype":"protein_coding","ncbi_id":"84939","summary":null,"start":1354711,"end":1378431,"strand":1,"description":"melanoma associated antigen (mutated) 1 [Source:HGNC Symbol;Acc:HGNC:29641]"}, {"versioned_ensembl_gene_id":"ENSG00000130558.19","gene_symbol":"OLFM1","gene_name":"olfactomedin 1 [Source:HGNC Symbol;Acc:HGNC:17187]","synonyms":"OlfA,NOELIN,NOE1,AMY","biotype":"protein_coding","ncbi_id":"10439","summary":"This gene product shares extensive sequence similarity with the rat neuronal olfactomedin-related ER localized protein. While the exact function of the encoded protein is not known, its abundant expression in brain suggests that it may have an essential role in nerve tissue. Several alternatively spliced transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":135075422,"end":135121179,"strand":1,"description":"olfactomedin 1 [Source:HGNC Symbol;Acc:HGNC:17187]"}, {"versioned_ensembl_gene_id":"ENSG00000236240.1","gene_symbol":"GPC5-IT1","gene_name":"GPC5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41340]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874293","summary":null,"start":92484606,"end":92510094,"strand":1,"description":"GPC5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41340]"}, {"versioned_ensembl_gene_id":"ENSG00000225368.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28986188,"end":28987469,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000100665.11","gene_symbol":"SERPINA4","gene_name":"serpin family A member 4 [Source:HGNC Symbol;Acc:HGNC:8948]","synonyms":"PI4,KST,KLST,kallistatin,KAL","biotype":"protein_coding","ncbi_id":"5267","summary":null,"start":94561091,"end":94569913,"strand":1,"description":"serpin family A member 4 [Source:HGNC Symbol;Acc:HGNC:8948]"}, {"versioned_ensembl_gene_id":"ENSG00000128422.15","gene_symbol":"KRT17","gene_name":"keratin 17 [Source:HGNC Symbol;Acc:HGNC:6427]","synonyms":"PCHC1","biotype":"protein_coding","ncbi_id":"3872","summary":"This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008]","start":41619437,"end":41624842,"strand":-1,"description":"keratin 17 [Source:HGNC Symbol;Acc:HGNC:6427]"}, {"versioned_ensembl_gene_id":"ENSG00000204439.3","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"D6S53E,G4","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31658298,"end":31660772,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000248883.2","gene_symbol":"B4GALNT2P1","gene_name":"beta-1,4-N-acetyl-galactosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51319]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481717","summary":null,"start":49085511,"end":49086702,"strand":1,"description":"beta-1,4-N-acetyl-galactosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51319]"}, {"versioned_ensembl_gene_id":"ENSG00000274387.1","gene_symbol":"AC097634.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71567863,"end":71571112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125457.13","gene_symbol":"MIF4GD","gene_name":"MIF4G domain containing [Source:HGNC Symbol;Acc:HGNC:24030]","synonyms":"SLIP1,MIFD,MGC45027,AD023","biotype":"protein_coding","ncbi_id":"57409","summary":"This gene encodes a protein which interacts with the N-terminus of the stem-loop binding protein (SLBP) and the 3' end of histone mRNA. This interaction facilitates the activation of histone mRNA translation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]","start":75266228,"end":75271227,"strand":-1,"description":"MIF4G domain containing [Source:HGNC Symbol;Acc:HGNC:24030]"}, {"versioned_ensembl_gene_id":"ENSG00000175287.18","gene_symbol":"PHYHD1","gene_name":"phytanoyl-CoA dioxygenase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23396]","synonyms":"MGC16638","biotype":"protein_coding","ncbi_id":"254295","summary":null,"start":128920895,"end":128942041,"strand":1,"description":"phytanoyl-CoA dioxygenase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23396]"}, {"versioned_ensembl_gene_id":"ENSG00000227515.3","gene_symbol":"C1DP4","gene_name":"C1D nuclear receptor corepressor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727879","summary":null,"start":80040621,"end":80041044,"strand":-1,"description":"C1D nuclear receptor corepressor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38028]"}, {"versioned_ensembl_gene_id":"ENSG00000260971.4","gene_symbol":"AC119674.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56154545,"end":56477687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229616.2","gene_symbol":"AL356095.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80017713,"end":80017911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232599.1","gene_symbol":"AL008707.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125203805,"end":125204338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254659.2","gene_symbol":"AP002444.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109751442,"end":109823847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170190.15","gene_symbol":"SLC16A5","gene_name":"solute carrier family 16 member 5 [Source:HGNC Symbol;Acc:HGNC:10926]","synonyms":"MCT6,MCT5","biotype":"protein_coding","ncbi_id":"9121","summary":"This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":75087727,"end":75106162,"strand":1,"description":"solute carrier family 16 member 5 [Source:HGNC Symbol;Acc:HGNC:10926]"}, {"versioned_ensembl_gene_id":"ENSG00000147677.10","gene_symbol":"EIF3H","gene_name":"eukaryotic translation initiation factor 3 subunit H [Source:HGNC Symbol;Acc:HGNC:3273]","synonyms":"EIF3S3,eIF3h,eIF3-p40,eIF3-gamma","biotype":"protein_coding","ncbi_id":"8667","summary":null,"start":116642130,"end":116766925,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit H [Source:HGNC Symbol;Acc:HGNC:3273]"}, {"versioned_ensembl_gene_id":"ENSG00000227559.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28896519,"end":28897311,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000118308.15","gene_symbol":"LRMP","gene_name":"lymphoid restricted membrane protein [Source:HGNC Symbol;Acc:HGNC:6690]","synonyms":"JAW1","biotype":"protein_coding","ncbi_id":"4033","summary":"The protein encode dby this gene is expressed in a developmentally regulated manner in lymphoid cell lines and tissues. The protein is localized to the cytoplasmic face of the endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":25004342,"end":25108334,"strand":1,"description":"lymphoid restricted membrane protein [Source:HGNC Symbol;Acc:HGNC:6690]"}, {"versioned_ensembl_gene_id":"ENSG00000229714.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"ZNF463P,dJ111M5.3","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28888821,"end":28889895,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000278982.1","gene_symbol":"AL139125.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7411599,"end":7413467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269148.1","gene_symbol":"AC092301.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45830164,"end":45831108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276794.1","gene_symbol":"AC108108.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70064043,"end":70134190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125755.18","gene_symbol":"SYMPK","gene_name":"symplekin [Source:HGNC Symbol;Acc:HGNC:22935]","synonyms":"SYM,SPK","biotype":"protein_coding","ncbi_id":"8189","summary":"This gene encodes a nuclear protein that functions in the regulation of polyadenylation and promotes gene expression. The protein forms a high-molecular weight complex with components of the polyadenylation machinery. It is thought to serve as a scaffold for recruiting regulatory factors to the polyadenylation complex. It also participates in 3'-end maturation of histone mRNAs, which do not undergo polyadenylation. The protein also localizes to the cytoplasmic plaques of tight junctions in some cell types. [provided by RefSeq, Jul 2008]","start":45815410,"end":45863290,"strand":-1,"description":"symplekin [Source:HGNC Symbol;Acc:HGNC:22935]"}, {"versioned_ensembl_gene_id":"ENSG00000109705.7","gene_symbol":"NKX3-2","gene_name":"NK3 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:951]","synonyms":"NKX3B,NKX3.2,BAPX1","biotype":"protein_coding","ncbi_id":"579","summary":"This gene encodes a member of the NK family of homeobox-containing proteins. The encoded protein may play a role in skeletal development. [provided by RefSeq, Jul 2008]","start":13540830,"end":13545050,"strand":-1,"description":"NK3 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:951]"}, {"versioned_ensembl_gene_id":"ENSG00000231703.2","gene_symbol":"AL354993.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53397661,"end":53412910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167862.9","gene_symbol":"MRPL58","gene_name":"mitochondrial ribosomal protein L58 [Source:HGNC Symbol;Acc:HGNC:5359]","synonyms":"ICT1,DS-1","biotype":"protein_coding","ncbi_id":"3396","summary":"The protein encoded by this gene is a peptidyl-tRNA hydrolase and a vital component of the large mitochondrial ribosome. The encoded protein serves as a ribosome release factor for this ribosome, which translates mitochondrial genes. This protein may be responsible for degrading prematurely-terminated polypeptides and for reusing stalled ribosomes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":75012670,"end":75021261,"strand":1,"description":"mitochondrial ribosomal protein L58 [Source:HGNC Symbol;Acc:HGNC:5359]"}, {"versioned_ensembl_gene_id":"ENSG00000182463.15","gene_symbol":"TSHZ2","gene_name":"teashirt zinc finger homeobox 2 [Source:HGNC Symbol;Acc:HGNC:13010]","synonyms":"C20orf17,ZNF218,ZABC2,TSH2,OVC10-2","biotype":"protein_coding","ncbi_id":"128553","summary":"This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and other types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":52972407,"end":53495330,"strand":1,"description":"teashirt zinc finger homeobox 2 [Source:HGNC Symbol;Acc:HGNC:13010]"}, {"versioned_ensembl_gene_id":"ENSG00000239521.7","gene_symbol":"GATS","gene_name":"GATS, stromal antigen 3 opposite strand [Source:HGNC Symbol;Acc:HGNC:29954]","synonyms":"STAG3OS,DKFZp686B07267","biotype":"protein_coding","ncbi_id":"352954","summary":null,"start":100200653,"end":100272218,"strand":-1,"description":"GATS, stromal antigen 3 opposite strand [Source:HGNC Symbol;Acc:HGNC:29954]"}, {"versioned_ensembl_gene_id":"ENSG00000188566.13","gene_symbol":"NDOR1","gene_name":"NADPH dependent diflavin oxidoreductase 1 [Source:HGNC Symbol;Acc:HGNC:29838]","synonyms":"NR1,bA350O14.9","biotype":"protein_coding","ncbi_id":"27158","summary":"This gene encodes an NADPH-dependent diflavin reductase that contains both flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) binding domains. The encoded protein catalyzes the transfer of electrons from NADPH through FAD and FMN cofactors to potential redox partners. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":137205685,"end":137217009,"strand":1,"description":"NADPH dependent diflavin oxidoreductase 1 [Source:HGNC Symbol;Acc:HGNC:29838]"}, {"versioned_ensembl_gene_id":"ENSG00000114841.17","gene_symbol":"DNAH1","gene_name":"dynein axonemal heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2940]","synonyms":"XLHSRF-1,HL11,HL-11,HDHC7,DNAHC1","biotype":"protein_coding","ncbi_id":"25981","summary":"This gene encodes an inner dynein arm heavy chain that provides structural support between the radial spokes and the outer doublet of the sperm tail. Naturally occurring mutations in this gene are associated with primary ciliary dyskinesia and multiple morphological anomalies of the flagella that result in asthenozoospermia and male infertility. Mice with a homozygous knockout of the orthologous gene are viable but have reduced sperm motility and are infertile. [provided by RefSeq, Feb 2017]","start":52316319,"end":52400491,"strand":1,"description":"dynein axonemal heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:2940]"}, {"versioned_ensembl_gene_id":"ENSG00000224530.1","gene_symbol":"PPIAP10","gene_name":"peptidylprolyl isomerase A pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:9264]","synonyms":"PPIP10,PPIAL2,CRP","biotype":"processed_pseudogene","ncbi_id":"140913","summary":null,"start":53421199,"end":53421656,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:9264]"}, {"versioned_ensembl_gene_id":"ENSG00000259723.1","gene_symbol":"AL354993.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53453058,"end":53504314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223492.1","gene_symbol":"AL391097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53168643,"end":53179550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227705.1","gene_symbol":"AL391097.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53196229,"end":53208705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271774.1","gene_symbol":"AL109930.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53255979,"end":53487274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280759.2","gene_symbol":"AP2A2","gene_name":"adaptor related protein complex 2 alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:562]","synonyms":"HIP9,DKFZP564D1864,CLAPA2,ADTAB,KIAA0899,HYPJ","biotype":"protein_coding","ncbi_id":"161","summary":"The protein encoded by this gene is a subunit of the AP-2 adaptor protein complex, which is involved in linking lipid and protein membrane components with the clathrin lattice. This interaction supports the formation of clathrin-coated vesicles, and the encoded subunit aids in the process by binding polyphosphoinositide-containing lipids in the cell membrane. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62789815,"end":62789885,"strand":1,"description":"microRNA 6748 [Source:HGNC Symbol;Acc:HGNC:50141]"}, {"versioned_ensembl_gene_id":"ENSG00000207235.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":59260748,"end":59260846,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276048.1","gene_symbol":"Six3os1_5","gene_name":"Six3os1 conserved region 5 [Source:RFAM;Acc:RF02250]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44937426,"end":44937696,"strand":1,"description":"Six3os1 conserved region 5 [Source:RFAM;Acc:RF02250]"}, {"versioned_ensembl_gene_id":"ENSG00000264574.1","gene_symbol":"MIR1254-2","gene_name":"microRNA 1254-2 [Source:HGNC Symbol;Acc:HGNC:41770]","synonyms":"hsa-mir-1254-2","biotype":"miRNA","ncbi_id":"100616217","summary":"This record was withdrawn by 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{"versioned_ensembl_gene_id":"ENSG00000240173.3","gene_symbol":"RN7SL771P","gene_name":"RNA, 7SL, cytoplasmic 771, pseudogene [Source:HGNC Symbol;Acc:HGNC:46787]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481132","summary":null,"start":140645829,"end":140646126,"strand":1,"description":"RNA, 7SL, cytoplasmic 771, pseudogene [Source:HGNC Symbol;Acc:HGNC:46787]"}, {"versioned_ensembl_gene_id":"ENSG00000276105.1","gene_symbol":"KCNQ1OT1_2","gene_name":"KCNQ1 overlapping transcript 1 conserved region 2 [Source:RFAM;Acc:RF01947]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2674097,"end":2674292,"strand":1,"description":"KCNQ1 overlapping transcript 1 conserved region 2 [Source:RFAM;Acc:RF01947]"}, {"versioned_ensembl_gene_id":"ENSG00000206795.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12149126,"end":12149238,"strand":1,"description":"Y RNA 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[provided by RefSeq, Sep 2009]","start":105621116,"end":105621180,"strand":1,"description":"microRNA 8071-1 [Source:HGNC Symbol;Acc:HGNC:50041]"}, {"versioned_ensembl_gene_id":"ENSG00000201793.1","gene_symbol":"RN7SKP9","gene_name":"RNA, 7SK small nuclear pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42627]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873853","summary":null,"start":99205708,"end":99206006,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42627]"}, {"versioned_ensembl_gene_id":"ENSG00000252026.1","gene_symbol":"RNU6-1262P","gene_name":"RNA, U6 small nuclear 1262, pseudogene [Source:HGNC Symbol;Acc:HGNC:48225]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480409","summary":null,"start":68284223,"end":68284318,"strand":-1,"description":"RNA, U6 small nuclear 1262, pseudogene [Source:HGNC Symbol;Acc:HGNC:48225]"}, {"versioned_ensembl_gene_id":"ENSG00000264757.1","gene_symbol":"MIR3198-1","gene_name":"microRNA 3198-1 [Source:HGNC Symbol;Acc:HGNC:38236]","synonyms":"MIR3198,hsa-mir-3198-1","biotype":"miRNA","ncbi_id":"100423025","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. 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[provided by RefSeq, Sep 2009]","start":17764180,"end":17764259,"strand":-1,"description":"microRNA 3198-1 [Source:HGNC Symbol;Acc:HGNC:38236]"}, {"versioned_ensembl_gene_id":"ENSG00000207257.1","gene_symbol":"RNU6-18P","gene_name":"RNA, U6 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:34262]","synonyms":"RNU6-18","biotype":"snRNA","ncbi_id":"106478916","summary":null,"start":32284152,"end":32284258,"strand":1,"description":"RNA, U6 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:34262]"}, {"versioned_ensembl_gene_id":"ENSG00000273843.1","gene_symbol":"AC009091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137798,"end":139135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266755.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31617447,"end":31617524,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000252656.1","gene_symbol":"RN7SKP88","gene_name":"RNA, 7SK small nuclear pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:45812]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480860","summary":null,"start":148839483,"end":148839732,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:45812]"}, {"versioned_ensembl_gene_id":"ENSG00000206846.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30673750,"end":30673843,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264549.1","gene_symbol":"SNORD95","gene_name":"small nucleolar RNA, C/D box 95 [Source:HGNC Symbol;Acc:HGNC:32757]","synonyms":"U95","biotype":"snoRNA","ncbi_id":"619570","summary":null,"start":181243312,"end":181243379,"strand":-1,"description":"small nucleolar RNA, C/D box 95 [Source:HGNC Symbol;Acc:HGNC:32757]"}, {"versioned_ensembl_gene_id":"ENSG00000200630.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":13160178,"end":13160279,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252164.1","gene_symbol":"RNA5SP282","gene_name":"RNA, 5S ribosomal pseudogene 282 [Source:HGNC Symbol;Acc:HGNC:43182]","synonyms":"RN5S282","biotype":"rRNA","ncbi_id":"100873535","summary":null,"start":34206134,"end":34206241,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 282 [Source:HGNC Symbol;Acc:HGNC:43182]"}, {"versioned_ensembl_gene_id":"ENSG00000276643.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":166099853,"end":166099924,"strand":1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000252898.1","gene_symbol":"RNU6-1096P","gene_name":"RNA, U6 small nuclear 1096, pseudogene [Source:HGNC Symbol;Acc:HGNC:48059]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480700","summary":null,"start":173446603,"end":173446704,"strand":-1,"description":"RNA, U6 small nuclear 1096, pseudogene [Source:HGNC Symbol;Acc:HGNC:48059]"}, {"versioned_ensembl_gene_id":"ENSG00000207344.1","gene_symbol":"SNORA22C","gene_name":"small nucleolar RNA, H/ACA box 22C [Source:HGNC Symbol;Acc:HGNC:52197]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616965","summary":null,"start":65065999,"end":65066132,"strand":1,"description":"small nucleolar RNA, H/ACA box 22C [Source:HGNC Symbol;Acc:HGNC:52197]"}, {"versioned_ensembl_gene_id":"ENSG00000266354.1","gene_symbol":"MIR4776-2","gene_name":"microRNA 4776-2 [Source:HGNC Symbol;Acc:HGNC:41631]","synonyms":"hsa-mir-4776-2","biotype":"miRNA","ncbi_id":"100616472","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. 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[provided by RefSeq, Sep 2009]","start":212926257,"end":212926336,"strand":1,"description":"microRNA 4776-2 [Source:HGNC Symbol;Acc:HGNC:41631]"}, {"versioned_ensembl_gene_id":"ENSG00000278825.1","gene_symbol":"RN7SL640P","gene_name":"RNA, 7SL, cytoplasmic 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:46656]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479456","summary":null,"start":39191100,"end":39191360,"strand":1,"description":"RNA, 7SL, cytoplasmic 640, pseudogene [Source:HGNC Symbol;Acc:HGNC:46656]"}, {"versioned_ensembl_gene_id":"ENSG00000221639.1","gene_symbol":"SNORA3","gene_name":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":73263960,"end":73264084,"strand":1,"description":"Small nucleolar RNA SNORA3/SNORA45 family [Source:RFAM;Acc:RF00334]"}, {"versioned_ensembl_gene_id":"ENSG00000201178.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32830219,"end":32830329,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274504.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. 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[provided by RefSeq, Mar 2009]","start":54988322,"end":55007215,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000251796.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":26247384,"end":26247521,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000238898.1","gene_symbol":"RNU1-80P","gene_name":"RNA, U1 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:48422]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480174","summary":null,"start":77920098,"end":77920258,"strand":1,"description":"RNA, U1 small nuclear 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:48422]"}, {"versioned_ensembl_gene_id":"ENSG00000251976.1","gene_symbol":"RN7SKP141","gene_name":"RNA, 7SK small nuclear pseudogene 141 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000222844.1","gene_symbol":"RNU6-321P","gene_name":"RNA, U6 small nuclear 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:47284]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479709","summary":null,"start":125277552,"end":125277657,"strand":1,"description":"RNA, U6 small nuclear 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:47284]"}, {"versioned_ensembl_gene_id":"ENSG00000201627.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105929126,"end":105929238,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202300.1","gene_symbol":"RNU6-487P","gene_name":"RNA, U6 small nuclear 487, pseudogene [Source:HGNC Symbol;Acc:HGNC:47450]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480393","summary":null,"start":203318996,"end":203319099,"strand":-1,"description":"RNA, U6 small nuclear 487, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252707.1","gene_symbol":"RNU11-2P","gene_name":"RNA, U11 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46942]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479561","summary":null,"start":12036496,"end":12036637,"strand":-1,"description":"RNA, U11 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:46942]"}, {"versioned_ensembl_gene_id":"ENSG00000252917.1","gene_symbol":"SNORA74","gene_name":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":42347061,"end":42347214,"strand":-1,"description":"Small nucleolar RNA SNORA74 [Source:RFAM;Acc:RF00090]"}, {"versioned_ensembl_gene_id":"ENSG00000242266.3","gene_symbol":"RN7SL456P","gene_name":"RNA, 7SL, cytoplasmic 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:46472]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480511","summary":null,"start":147940007,"end":147940301,"strand":1,"description":"RNA, 7SL, cytoplasmic 456, pseudogene [Source:HGNC Symbol;Acc:HGNC:46472]"}, {"versioned_ensembl_gene_id":"ENSG00000207058.1","gene_symbol":"RNU6-784P","gene_name":"RNA, U6 small nuclear 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:47747]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481428","summary":null,"start":70703018,"end":70703123,"strand":-1,"description":"RNA, U6 small nuclear 784, pseudogene [Source:HGNC Symbol;Acc:HGNC:47747]"}, {"versioned_ensembl_gene_id":"ENSG00000266274.2","gene_symbol":"RN7SL138P","gene_name":"RNA, 7SL, cytoplasmic 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:46154]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480489","summary":null,"start":30959564,"end":30959850,"strand":1,"description":"RNA, 7SL, cytoplasmic 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:46154]"}, {"versioned_ensembl_gene_id":"ENSG00000207127.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49416744,"end":49416850,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275948.1","gene_symbol":"mascRNA-menRNA","gene_name":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":65445541,"end":65445598,"strand":1,"description":"MALAT1-associated small cytoplasmic RNA/MEN beta RNA [Source:RFAM;Acc:RF01684]"}, {"versioned_ensembl_gene_id":"ENSG00000199480.1","gene_symbol":"RNA5SP389","gene_name":"RNA, 5S ribosomal pseudogene 389 [Source:HGNC Symbol;Acc:HGNC:43289]","synonyms":"RN5S389","biotype":"rRNA","ncbi_id":"106480766","summary":null,"start":106636672,"end":106636786,"strand":1,"description":"RNA, 5S ribosomal pseudogene 389 [Source:HGNC Symbol;Acc:HGNC:43289]"}, {"versioned_ensembl_gene_id":"ENSG00000201376.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":51244090,"end":51244224,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000263491.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28977485,"end":28977783,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000243870.3","gene_symbol":"RN7SL236P","gene_name":"RNA, 7SL, cytoplasmic 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:46252]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480986","summary":null,"start":78370852,"end":78371135,"strand":-1,"description":"RNA, 7SL, cytoplasmic 236, pseudogene [Source:HGNC Symbol;Acc:HGNC:46252]"}, {"versioned_ensembl_gene_id":"ENSG00000273587.1","gene_symbol":"SNORA78","gene_name":"small nucleolar RNA, H/ACA box 78 [Source:HGNC Symbol;Acc:HGNC:32664]","synonyms":"ACA64","biotype":"snoRNA","ncbi_id":"677844","summary":null,"start":1965184,"end":1965310,"strand":1,"description":"small nucleolar RNA, H/ACA box 78 [Source:HGNC Symbol;Acc:HGNC:32664]"}, {"versioned_ensembl_gene_id":"ENSG00000199994.1","gene_symbol":"RNA5SP145","gene_name":"RNA, 5S ribosomal pseudogene 145 [Source:HGNC Symbol;Acc:HGNC:43045]","synonyms":"RN5S145","biotype":"rRNA","ncbi_id":"100873412","summary":null,"start":151188099,"end":151188223,"strand":1,"description":"RNA, 5S ribosomal pseudogene 145 [Source:HGNC Symbol;Acc:HGNC:43045]"}, {"versioned_ensembl_gene_id":"ENSG00000207483.1","gene_symbol":"RNU6-1067P","gene_name":"RNA, U6 small nuclear 1067, pseudogene [Source:HGNC Symbol;Acc:HGNC:48030]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481516","summary":null,"start":28667919,"end":28668025,"strand":1,"description":"RNA, U6 small nuclear 1067, pseudogene [Source:HGNC Symbol;Acc:HGNC:48030]"}, {"versioned_ensembl_gene_id":"ENSG00000238324.1","gene_symbol":"RN7SKP198","gene_name":"RNA, 7SK small nuclear pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:45922]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479183","summary":null,"start":102857450,"end":102857755,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 198 [Source:HGNC Symbol;Acc:HGNC:45922]"}, {"versioned_ensembl_gene_id":"ENSG00000265957.1","gene_symbol":"MIR4319","gene_name":"microRNA 4319 [Source:HGNC Symbol;Acc:HGNC:38212]","synonyms":"hsa-mir-4319","biotype":"miRNA","ncbi_id":"100422829","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44970082,"end":44970166,"strand":-1,"description":"microRNA 4319 [Source:HGNC Symbol;Acc:HGNC:38212]"}, {"versioned_ensembl_gene_id":"ENSG00000207743.3","gene_symbol":"MIR495","gene_name":"microRNA 495 [Source:HGNC Symbol;Acc:HGNC:32085]","synonyms":"MIRN495,hsa-mir-495","biotype":"miRNA","ncbi_id":"574453","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101033755,"end":101033836,"strand":1,"description":"microRNA 495 [Source:HGNC Symbol;Acc:HGNC:32085]"}, {"versioned_ensembl_gene_id":"ENSG00000276102.1","gene_symbol":"MIR6747","gene_name":"microRNA 6747 [Source:HGNC Symbol;Acc:HGNC:50027]","synonyms":"hsa-mir-6747","biotype":"miRNA","ncbi_id":"102465447","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62567011,"end":62567071,"strand":-1,"description":"microRNA 6747 [Source:HGNC Symbol;Acc:HGNC:50027]"}, {"versioned_ensembl_gene_id":"ENSG00000207202.1","gene_symbol":"RNU6-800P","gene_name":"RNA, U6 small nuclear 800, pseudogene [Source:HGNC Symbol;Acc:HGNC:47763]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481433","summary":null,"start":10582817,"end":10582919,"strand":1,"description":"RNA, U6 small nuclear 800, pseudogene [Source:HGNC Symbol;Acc:HGNC:47763]"}, {"versioned_ensembl_gene_id":"ENSG00000276788.1","gene_symbol":"SNORD26","gene_name":"small nucleolar RNA, C/D box 26 [Source:HGNC Symbol;Acc:HGNC:10148]","synonyms":"U26,RNU26","biotype":"snoRNA","ncbi_id":"9302","summary":null,"start":62855292,"end":62855366,"strand":-1,"description":"small nucleolar RNA, C/D box 26 [Source:HGNC Symbol;Acc:HGNC:10148]"}, {"versioned_ensembl_gene_id":"ENSG00000223294.1","gene_symbol":"SNORD83","gene_name":"Small nucleolar RNA SNORD83 [Source:RFAM;Acc:RF00137]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64575665,"end":64575741,"strand":1,"description":"Small nucleolar RNA SNORD83 [Source:RFAM;Acc:RF00137]"}, {"versioned_ensembl_gene_id":"ENSG00000252258.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"RNU70,U70,DXS648E","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":3025434,"end":3025566,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000212598.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":90030284,"end":90030495,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000278782.1","gene_symbol":"AC136616.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1157687,"end":1240349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275551.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000212576.1","gene_symbol":"RNA5SP467","gene_name":"RNA, 5S ribosomal pseudogene 467 [Source:HGNC Symbol;Acc:HGNC:43367]","synonyms":"RN5S467","biotype":"rRNA","ncbi_id":"100873711","summary":null,"start":12106497,"end":12106614,"strand":1,"description":"RNA, 5S ribosomal pseudogene 467 [Source:HGNC Symbol;Acc:HGNC:43367]"}, {"versioned_ensembl_gene_id":"ENSG00000240577.3","gene_symbol":"RN7SL445P","gene_name":"RNA, 7SL, cytoplasmic 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:46461]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481044","summary":null,"start":5631463,"end":5631755,"strand":1,"description":"RNA, 7SL, cytoplasmic 445, pseudogene [Source:HGNC Symbol;Acc:HGNC:46461]"}, {"versioned_ensembl_gene_id":"ENSG00000252999.1","gene_symbol":"RNA5SP380","gene_name":"RNA, 5S ribosomal pseudogene 380 [Source:HGNC Symbol;Acc:HGNC:43280]","synonyms":"RN5S380","biotype":"rRNA","ncbi_id":"100873636","summary":null,"start":20090130,"end":20090227,"strand":1,"description":"RNA, 5S ribosomal pseudogene 380 [Source:HGNC Symbol;Acc:HGNC:43280]"}, {"versioned_ensembl_gene_id":"ENSG00000238390.1","gene_symbol":"SNORA81","gene_name":"Small nucleolar RNA SNORA81 [Source:RFAM;Acc:RF01241]","synonyms":"HBI-61","biotype":"snoRNA","ncbi_id":"677847","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA81, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":31664306,"end":31664482,"strand":1,"description":"Small nucleolar RNA SNORA81 [Source:RFAM;Acc:RF01241]"}, {"versioned_ensembl_gene_id":"ENSG00000206599.1","gene_symbol":"RNU6-841P","gene_name":"RNA, U6 small nuclear 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:47804]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480699","summary":null,"start":49764524,"end":49764630,"strand":-1,"description":"RNA, U6 small nuclear 841, pseudogene [Source:HGNC Symbol;Acc:HGNC:47804]"}, {"versioned_ensembl_gene_id":"ENSG00000207182.1","gene_symbol":"RNU1-44P","gene_name":"RNA, U1 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48386]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480160","summary":null,"start":146580048,"end":146580210,"strand":1,"description":"RNA, U1 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:48386]"}, {"versioned_ensembl_gene_id":"ENSG00000277777.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":5597390,"end":5597490,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239153.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":115627082,"end":115627185,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000278104.1","gene_symbol":"ZNRD1-AS1_1","gene_name":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30035916,"end":30035983,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]"}, {"versioned_ensembl_gene_id":"ENSG00000201050.1","gene_symbol":"RNU6-668P","gene_name":"RNA, U6 small nuclear 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:47631]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481393","summary":null,"start":164787290,"end":164787396,"strand":1,"description":"RNA, U6 small nuclear 668, pseudogene [Source:HGNC Symbol;Acc:HGNC:47631]"}, {"versioned_ensembl_gene_id":"ENSG00000252744.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":148330271,"end":148330394,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277071.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7,PYPAF3","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54867507,"end":54891503,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000274040.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23169365,"end":23169654,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201033.1","gene_symbol":"RNU1-96P","gene_name":"RNA, U1 small nuclear 96, pseudogene [Source:HGNC Symbol;Acc:HGNC:48438]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480181","summary":null,"start":27513871,"end":27514032,"strand":1,"description":"RNA, U1 small nuclear 96, pseudogene [Source:HGNC Symbol;Acc:HGNC:48438]"}, {"versioned_ensembl_gene_id":"ENSG00000251810.1","gene_symbol":"RN7SKP132","gene_name":"RNA, 7SK small nuclear pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:45856]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480874","summary":null,"start":27783846,"end":27784053,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:45856]"}, {"versioned_ensembl_gene_id":"ENSG00000212611.1","gene_symbol":"SNORD30","gene_name":"Small nucleolar RNA SNORD30 [Source:RFAM;Acc:RF00088]","synonyms":"U30,RNU30","biotype":"snoRNA","ncbi_id":"9299","summary":null,"start":114017033,"end":114017102,"strand":1,"description":"Small nucleolar RNA SNORD30 [Source:RFAM;Acc:RF00088]"}, {"versioned_ensembl_gene_id":"ENSG00000275174.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":21428879,"end":21428985,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000252711.1","gene_symbol":"RN7SKP116","gene_name":"RNA, 7SK small nuclear pseudogene 116 [Source:HGNC Symbol;Acc:HGNC:45840]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480869","summary":null,"start":47715283,"end":47715601,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 116 [Source:HGNC Symbol;Acc:HGNC:45840]"}, {"versioned_ensembl_gene_id":"ENSG00000201623.1","gene_symbol":"RNU6-923P","gene_name":"RNA, U6 small nuclear 923, pseudogene [Source:HGNC Symbol;Acc:HGNC:47886]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481471","summary":null,"start":33888056,"end":33888162,"strand":-1,"description":"RNA, U6 small nuclear 923, pseudogene [Source:HGNC Symbol;Acc:HGNC:47886]"}, {"versioned_ensembl_gene_id":"ENSG00000199933.1","gene_symbol":"RNY1P16","gene_name":"RNA, Ro-associated Y1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50879]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480312","summary":null,"start":101719808,"end":101719918,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:50879]"}, {"versioned_ensembl_gene_id":"ENSG00000277308.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97297290,"end":97297557,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283969.1","gene_symbol":"MIR6838","gene_name":"microRNA 6838 [Source:HGNC Symbol;Acc:HGNC:50050]","synonyms":"hsa-mir-6838","biotype":"miRNA","ncbi_id":"102465504","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44073378,"end":44073433,"strand":-1,"description":"microRNA 6838 [Source:HGNC Symbol;Acc:HGNC:50050]"}, {"versioned_ensembl_gene_id":"ENSG00000275166.1","gene_symbol":"MIR6814","gene_name":"microRNA 6814 [Source:HGNC Symbol;Acc:HGNC:50145]","synonyms":"hsa-mir-6814","biotype":"miRNA","ncbi_id":"102465488","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41746772,"end":41746841,"strand":-1,"description":"microRNA 6814 [Source:HGNC Symbol;Acc:HGNC:50145]"}, {"versioned_ensembl_gene_id":"ENSG00000199251.1","gene_symbol":"RNU6-664P","gene_name":"RNA, U6 small nuclear 664, pseudogene [Source:HGNC Symbol;Acc:HGNC:47627]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479861","summary":null,"start":207680533,"end":207680639,"strand":-1,"description":"RNA, U6 small nuclear 664, pseudogene [Source:HGNC Symbol;Acc:HGNC:47627]"}, {"versioned_ensembl_gene_id":"ENSG00000206751.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72853224,"end":72853331,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252765.1","gene_symbol":"SCARNA16","gene_name":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]","synonyms":"ACA47","biotype":"scaRNA","ncbi_id":"677781","summary":null,"start":101133153,"end":101133339,"strand":1,"description":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]"}, {"versioned_ensembl_gene_id":"ENSG00000264897.1","gene_symbol":"MIR3921","gene_name":"microRNA 3921 [Source:HGNC Symbol;Acc:HGNC:38936]","synonyms":"hsa-mir-3921","biotype":"miRNA","ncbi_id":"100500859","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99964314,"end":99964398,"strand":-1,"description":"microRNA 3921 [Source:HGNC Symbol;Acc:HGNC:38936]"}, {"versioned_ensembl_gene_id":"ENSG00000274121.1","gene_symbol":"DISC2","gene_name":"Disrupted in schizophrenia 2 conserved region [Source:RFAM;Acc:RF02102]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"27184","summary":"DISC2 is thought to specify a noncoding RNA molecule antisense to DISC1 (MIM 605210). Both genes were found to be disrupted by a translocation in a large schizophrenia (MIM 181500) kindred.[supplied by OMIM, Jul 2002]","start":231814982,"end":231815186,"strand":1,"description":"Disrupted in schizophrenia 2 conserved region [Source:RFAM;Acc:RF02102]"}, {"versioned_ensembl_gene_id":"ENSG00000266594.1","gene_symbol":"MIR4766","gene_name":"microRNA 4766 [Source:HGNC Symbol;Acc:HGNC:41680]","synonyms":"hsa-mir-4766","biotype":"miRNA","ncbi_id":"100616283","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40813883,"end":40813958,"strand":-1,"description":"microRNA 4766 [Source:HGNC Symbol;Acc:HGNC:41680]"}, {"versioned_ensembl_gene_id":"ENSG00000284520.1","gene_symbol":"MIRLET7B","gene_name":"microRNA let-7b [Source:HGNC Symbol;Acc:HGNC:31479]","synonyms":"MIRNLET7B,hsa-let-7b","biotype":"miRNA","ncbi_id":"406884","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46113686,"end":46113768,"strand":1,"description":"microRNA let-7b [Source:HGNC Symbol;Acc:HGNC:31479]"}, {"versioned_ensembl_gene_id":"ENSG00000284419.1","gene_symbol":"MIR663A","gene_name":"microRNA 663a [Source:HGNC Symbol;Acc:HGNC:32919]","synonyms":"MIRN663,MIR663,hsa-mir-663","biotype":"miRNA","ncbi_id":"724033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26208186,"end":26208278,"strand":-1,"description":"microRNA 663a [Source:HGNC Symbol;Acc:HGNC:32919]"}, {"versioned_ensembl_gene_id":"ENSG00000212312.1","gene_symbol":"RNA5SP109","gene_name":"RNA, 5S ribosomal pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:42907]","synonyms":"RN5S109","biotype":"rRNA","ncbi_id":"100873379","summary":null,"start":162496936,"end":162497051,"strand":1,"description":"RNA, 5S ribosomal pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:42907]"}, {"versioned_ensembl_gene_id":"ENSG00000252764.1","gene_symbol":"RNU6-1092P","gene_name":"RNA, U6 small nuclear 1092, pseudogene [Source:HGNC Symbol;Acc:HGNC:48055]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480046","summary":null,"start":100683488,"end":100683574,"strand":1,"description":"RNA, U6 small nuclear 1092, pseudogene [Source:HGNC Symbol;Acc:HGNC:48055]"}, {"versioned_ensembl_gene_id":"ENSG00000251922.1","gene_symbol":"SNORA14","gene_name":"Small nucleolar RNA SNORA14 [Source:RFAM;Acc:RF00397]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":6017054,"end":6017194,"strand":-1,"description":"Small nucleolar RNA SNORA14 [Source:RFAM;Acc:RF00397]"}, {"versioned_ensembl_gene_id":"ENSG00000252094.1","gene_symbol":"RNA5SP410","gene_name":"RNA, 5S ribosomal pseudogene 410 [Source:HGNC Symbol;Acc:HGNC:43310]","synonyms":"RN5S410","biotype":"rRNA","ncbi_id":"100873662","summary":null,"start":35745989,"end":35746094,"strand":1,"description":"RNA, 5S ribosomal pseudogene 410 [Source:HGNC Symbol;Acc:HGNC:43310]"}, {"versioned_ensembl_gene_id":"ENSG00000206587.1","gene_symbol":"RNU6-46P","gene_name":"RNA, U6 small nuclear 46, pseudogene [Source:HGNC Symbol;Acc:HGNC:34290]","synonyms":"RNU6-46","biotype":"snRNA","ncbi_id":"100873760","summary":null,"start":67895631,"end":67895737,"strand":1,"description":"RNA, U6 small nuclear 46, pseudogene [Source:HGNC Symbol;Acc:HGNC:34290]"}, {"versioned_ensembl_gene_id":"ENSG00000202059.1","gene_symbol":"SNORA1","gene_name":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]","synonyms":"ACA1","biotype":"snoRNA","ncbi_id":"677792","summary":null,"start":203052285,"end":203052418,"strand":-1,"description":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]"}, {"versioned_ensembl_gene_id":"ENSG00000202074.1","gene_symbol":"RNU6-715P","gene_name":"RNA, U6 small nuclear 715, pseudogene [Source:HGNC Symbol;Acc:HGNC:47678]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481405","summary":null,"start":147495438,"end":147495540,"strand":-1,"description":"RNA, U6 small nuclear 715, pseudogene [Source:HGNC Symbol;Acc:HGNC:47678]"}, {"versioned_ensembl_gene_id":"ENSG00000223003.1","gene_symbol":"RNA5SP184","gene_name":"RNA, 5S ribosomal pseudogene 184 [Source:HGNC Symbol;Acc:HGNC:43084]","synonyms":"RN5S184","biotype":"rRNA","ncbi_id":"100873446","summary":null,"start":56146739,"end":56146846,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 184 [Source:HGNC Symbol;Acc:HGNC:43084]"}, {"versioned_ensembl_gene_id":"ENSG00000277927.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":156089,"end":156195,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000278039.1","gene_symbol":"Xist_exon1","gene_name":"X-chromosome inactivation gene exon 1 [Source:RFAM;Acc:RF01880]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73850487,"end":73850571,"strand":1,"description":"X-chromosome inactivation gene exon 1 [Source:RFAM;Acc:RF01880]"}, {"versioned_ensembl_gene_id":"ENSG00000252804.1","gene_symbol":"RNU6-958P","gene_name":"RNA, U6 small nuclear 958, pseudogene [Source:HGNC Symbol;Acc:HGNC:47921]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481482","summary":null,"start":43408307,"end":43408412,"strand":1,"description":"RNA, U6 small nuclear 958, pseudogene [Source:HGNC Symbol;Acc:HGNC:47921]"}, {"versioned_ensembl_gene_id":"ENSG00000274788.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54709037,"end":54713341,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284498.1","gene_symbol":"MIR564","gene_name":"microRNA 564 [Source:HGNC Symbol;Acc:HGNC:32820]","synonyms":"MIRN564,hsa-mir-564","biotype":"miRNA","ncbi_id":"693149","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44861888,"end":44861981,"strand":1,"description":"microRNA 564 [Source:HGNC Symbol;Acc:HGNC:32820]"}, {"versioned_ensembl_gene_id":"ENSG00000199784.1","gene_symbol":"RNU6-1287P","gene_name":"RNA, U6 small nuclear 1287, pseudogene [Source:HGNC Symbol;Acc:HGNC:48250]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480127","summary":null,"start":56274530,"end":56274636,"strand":-1,"description":"RNA, U6 small nuclear 1287, pseudogene [Source:HGNC Symbol;Acc:HGNC:48250]"}, {"versioned_ensembl_gene_id":"ENSG00000207803.1","gene_symbol":"MIR518A1","gene_name":"microRNA 518a-1 [Source:HGNC Symbol;Acc:HGNC:32120]","synonyms":"MIRN518A1,MIRN518A-1,hsa-mir-518a-1","biotype":"miRNA","ncbi_id":"574488","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53731006,"end":53731090,"strand":1,"description":"microRNA 518a-1 [Source:HGNC Symbol;Acc:HGNC:32120]"}, {"versioned_ensembl_gene_id":"ENSG00000200326.1","gene_symbol":"RNA5SP391","gene_name":"RNA, 5S ribosomal pseudogene 391 [Source:HGNC Symbol;Acc:HGNC:43291]","synonyms":"RN5S391","biotype":"rRNA","ncbi_id":"100873644","summary":null,"start":27280318,"end":27280436,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 391 [Source:HGNC Symbol;Acc:HGNC:43291]"}, {"versioned_ensembl_gene_id":"ENSG00000274999.1","gene_symbol":"MIR8052","gene_name":"microRNA 8052 [Source:HGNC Symbol;Acc:HGNC:50252]","synonyms":"hsa-mir-8052","biotype":"miRNA","ncbi_id":"102466873","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130666735,"end":130666803,"strand":1,"description":"microRNA 8052 [Source:HGNC Symbol;Acc:HGNC:50252]"}, {"versioned_ensembl_gene_id":"ENSG00000200709.1","gene_symbol":"RNA5SP27","gene_name":"RNA, 5S ribosomal pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42603]","synonyms":"RN5S27","biotype":"rRNA","ncbi_id":"100873359","summary":null,"start":45551485,"end":45551603,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42603]"}, {"versioned_ensembl_gene_id":"ENSG00000212387.1","gene_symbol":"RNU6-1055P","gene_name":"RNA, U6 small nuclear 1055, pseudogene [Source:HGNC Symbol;Acc:HGNC:48018]","synonyms":null,"biotype":"snRNA","ncbi_id":"107105256","summary":null,"start":186501109,"end":186501215,"strand":1,"description":"RNA, U6 small nuclear 1055, pseudogene [Source:HGNC Symbol;Acc:HGNC:48018]"}, {"versioned_ensembl_gene_id":"ENSG00000196274.5","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":76230048,"end":76230390,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238694.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":34966241,"end":34966344,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000200101.1","gene_symbol":"RNU6-508P","gene_name":"RNA, U6 small nuclear 508, pseudogene [Source:HGNC Symbol;Acc:HGNC:47471]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480585","summary":null,"start":59647621,"end":59647723,"strand":1,"description":"RNA, U6 small nuclear 508, pseudogene [Source:HGNC Symbol;Acc:HGNC:47471]"}, {"versioned_ensembl_gene_id":"ENSG00000251729.1","gene_symbol":"RNA5SP401","gene_name":"RNA, 5S ribosomal pseudogene 401 [Source:HGNC Symbol;Acc:HGNC:43301]","synonyms":"RN5S401","biotype":"rRNA","ncbi_id":"100873654","summary":null,"start":97472126,"end":97472252,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 401 [Source:HGNC Symbol;Acc:HGNC:43301]"}, {"versioned_ensembl_gene_id":"ENSG00000278756.1","gene_symbol":"MIR6722","gene_name":"microRNA 6722 [Source:HGNC Symbol;Acc:HGNC:49927]","synonyms":"hsa-mir-6722","biotype":"miRNA","ncbi_id":"102465431","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136746893,"end":136746970,"strand":-1,"description":"microRNA 6722 [Source:HGNC Symbol;Acc:HGNC:49927]"}, {"versioned_ensembl_gene_id":"ENSG00000265920.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32310327,"end":32310433,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000243373.3","gene_symbol":"RN7SL173P","gene_name":"RNA, 7SL, cytoplasmic 173, pseudogene [Source:HGNC Symbol;Acc:HGNC:46189]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479284","summary":null,"start":158437797,"end":158438088,"strand":1,"description":"RNA, 7SL, cytoplasmic 173, pseudogene [Source:HGNC Symbol;Acc:HGNC:46189]"}, {"versioned_ensembl_gene_id":"ENSG00000184185.9","gene_symbol":"KCNJ12","gene_name":"potassium voltage-gated channel subfamily J member 12 [Source:HGNC Symbol;Acc:HGNC:6258]","synonyms":"Kir2.2v,Kir2.2,KCNJN1,IRK2,hIRK1","biotype":"protein_coding","ncbi_id":"3768","summary":"This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":21376197,"end":21419872,"strand":1,"description":"potassium voltage-gated channel subfamily J member 12 [Source:HGNC Symbol;Acc:HGNC:6258]"}, {"versioned_ensembl_gene_id":"ENSG00000279454.1","gene_symbol":"AP003499.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93587703,"end":93588559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249631.5","gene_symbol":"AC005699.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11625714,"end":11813958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251536.2","gene_symbol":"AC055717.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129852208,"end":129854944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266104.1","gene_symbol":"MIR4326","gene_name":"microRNA 4326 [Source:HGNC Symbol;Acc:HGNC:38314]","synonyms":"hsa-mir-4326","biotype":"miRNA","ncbi_id":"100422945","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63286808,"end":63286866,"strand":1,"description":"microRNA 4326 [Source:HGNC Symbol;Acc:HGNC:38314]"}, {"versioned_ensembl_gene_id":"ENSG00000207773.1","gene_symbol":"MIR642A","gene_name":"microRNA 642a [Source:HGNC Symbol;Acc:HGNC:32898]","synonyms":"MIRN642,MIR642,hsa-mir-642","biotype":"miRNA","ncbi_id":"693227","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45674928,"end":45675024,"strand":1,"description":"microRNA 642a [Source:HGNC Symbol;Acc:HGNC:32898]"}, {"versioned_ensembl_gene_id":"ENSG00000212266.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":117688621,"end":117688742,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000283721.1","gene_symbol":"MIR6884","gene_name":"microRNA 6884 [Source:HGNC Symbol;Acc:HGNC:50091]","synonyms":"hsa-mir-6884","biotype":"miRNA","ncbi_id":"102466757","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40026332,"end":40026409,"strand":-1,"description":"microRNA 6884 [Source:HGNC Symbol;Acc:HGNC:50091]"}, {"versioned_ensembl_gene_id":"ENSG00000207934.1","gene_symbol":"MIR654","gene_name":"microRNA 654 [Source:HGNC Symbol;Acc:HGNC:32910]","synonyms":"MIRN654,hsa-mir-654","biotype":"miRNA","ncbi_id":"724024","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101040219,"end":101040299,"strand":1,"description":"microRNA 654 [Source:HGNC Symbol;Acc:HGNC:32910]"}, {"versioned_ensembl_gene_id":"ENSG00000275967.1","gene_symbol":"MIR6880","gene_name":"microRNA 6880 [Source:HGNC Symbol;Acc:HGNC:50187]","synonyms":"hsa-mir-6880","biotype":"miRNA","ncbi_id":"102466204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124337181,"end":124337242,"strand":-1,"description":"microRNA 6880 [Source:HGNC Symbol;Acc:HGNC:50187]"}, {"versioned_ensembl_gene_id":"ENSG00000222795.1","gene_symbol":"RNU4-83P","gene_name":"RNA, U4 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:47019]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479596","summary":null,"start":100831728,"end":100831860,"strand":-1,"description":"RNA, U4 small nuclear 83, pseudogene [Source:HGNC Symbol;Acc:HGNC:47019]"}, {"versioned_ensembl_gene_id":"ENSG00000200786.1","gene_symbol":"RNA5SP234","gene_name":"RNA, 5S ribosomal pseudogene 234 [Source:HGNC Symbol;Acc:HGNC:43134]","synonyms":"RN5S234","biotype":"rRNA","ncbi_id":"100873492","summary":null,"start":79654109,"end":79654227,"strand":1,"description":"RNA, 5S ribosomal pseudogene 234 [Source:HGNC Symbol;Acc:HGNC:43134]"}, {"versioned_ensembl_gene_id":"ENSG00000274868.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8388898,"end":8388987,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000212325.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100398352,"end":100398446,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212528.1","gene_symbol":"SNORD115-47","gene_name":"small nucleolar RNA, C/D box 115-47 [Source:HGNC Symbol;Acc:HGNC:33065]","synonyms":"HBII-52-47","biotype":"snoRNA","ncbi_id":"100036567","summary":null,"start":25268466,"end":25268551,"strand":1,"description":"small nucleolar RNA, C/D box 115-47 [Source:HGNC Symbol;Acc:HGNC:33065]"}, {"versioned_ensembl_gene_id":"ENSG00000199866.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":172558151,"end":172558252,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000126464.13","gene_symbol":"PRR12","gene_name":"proline rich 12 [Source:HGNC Symbol;Acc:HGNC:29217]","synonyms":"KIAA1205","biotype":"protein_coding","ncbi_id":"57479","summary":"This gene encodes a proline-rich protein that contains two A-T hook DNA binding domains. A chromosomal translocation and gene fusion between this gene and zinc finger, MIZ-type containing 1 (Gene ID: 57178) may underlie intellectual disability and neuropsychiatric problems in a human patient. Enriched expression of this gene in embryonic mouse brain suggests that this gene may play a role in nervous system development. [provided by RefSeq, Jul 2016]","start":49591643,"end":49626439,"strand":1,"description":"proline rich 12 [Source:HGNC Symbol;Acc:HGNC:29217]"}, {"versioned_ensembl_gene_id":"ENSG00000284440.1","gene_symbol":"MIR122","gene_name":"microRNA 122 [Source:HGNC Symbol;Acc:HGNC:31501]","synonyms":"MIRN122A,MIRN122,hsa-mir-122a,hsa-mir-122","biotype":"miRNA","ncbi_id":"406906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58451074,"end":58451158,"strand":1,"description":"microRNA 122 [Source:HGNC Symbol;Acc:HGNC:31501]"}, {"versioned_ensembl_gene_id":"ENSG00000222624.1","gene_symbol":"RNU2-15P","gene_name":"RNA, U2 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:48508]","synonyms":null,"biotype":"snRNA","ncbi_id":"106866980","summary":null,"start":65415816,"end":65416006,"strand":1,"description":"RNA, U2 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:48508]"}, {"versioned_ensembl_gene_id":"ENSG00000264386.1","gene_symbol":"MIR4513","gene_name":"microRNA 4513 [Source:HGNC Symbol;Acc:HGNC:41855]","synonyms":"hsa-mir-4513","biotype":"miRNA","ncbi_id":"100616183","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74788672,"end":74788757,"strand":-1,"description":"microRNA 4513 [Source:HGNC Symbol;Acc:HGNC:41855]"}, {"versioned_ensembl_gene_id":"ENSG00000199739.1","gene_symbol":"RNU6-552P","gene_name":"RNA, U6 small nuclear 552, pseudogene [Source:HGNC Symbol;Acc:HGNC:47515]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481356","summary":null,"start":45274359,"end":45274477,"strand":-1,"description":"RNA, U6 small nuclear 552, pseudogene [Source:HGNC Symbol;Acc:HGNC:47515]"}, {"versioned_ensembl_gene_id":"ENSG00000221325.1","gene_symbol":"MIR1200","gene_name":"microRNA 1200 [Source:HGNC Symbol;Acc:HGNC:35266]","synonyms":"MIRN1200,hsa-mir-1200","biotype":"miRNA","ncbi_id":"100302113","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36919357,"end":36919432,"strand":-1,"description":"microRNA 1200 [Source:HGNC Symbol;Acc:HGNC:35266]"}, {"versioned_ensembl_gene_id":"ENSG00000263418.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32117921,"end":32118041,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000283335.1","gene_symbol":"MIR219B","gene_name":"microRNA 219b [Source:HGNC Symbol;Acc:HGNC:41823]","synonyms":"MIR2964A,hsa-mir-2964a","biotype":"miRNA","ncbi_id":"100616335","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128392621,"end":128392708,"strand":1,"description":"microRNA 219b [Source:HGNC Symbol;Acc:HGNC:41823]"}, {"versioned_ensembl_gene_id":"ENSG00000252027.1","gene_symbol":"RNU6ATAC14P","gene_name":"RNA, U6atac small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46913]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481163","summary":null,"start":176664676,"end":176664766,"strand":1,"description":"RNA, U6atac small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46913]"}, {"versioned_ensembl_gene_id":"ENSG00000252307.1","gene_symbol":"RNA5SP153","gene_name":"RNA, 5S ribosomal pseudogene 153 [Source:HGNC Symbol;Acc:HGNC:43053]","synonyms":"RN5S153","biotype":"rRNA","ncbi_id":"100873419","summary":null,"start":9411178,"end":9411253,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 153 [Source:HGNC Symbol;Acc:HGNC:43053]"}, {"versioned_ensembl_gene_id":"ENSG00000201386.1","gene_symbol":"RNU6-1163P","gene_name":"RNA, U6 small nuclear 1163, pseudogene [Source:HGNC Symbol;Acc:HGNC:48126]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481547","summary":null,"start":112971493,"end":112971599,"strand":1,"description":"RNA, U6 small nuclear 1163, pseudogene [Source:HGNC Symbol;Acc:HGNC:48126]"}, {"versioned_ensembl_gene_id":"ENSG00000206980.1","gene_symbol":"RNU6-662P","gene_name":"RNA, U6 small nuclear 662, pseudogene [Source:HGNC Symbol;Acc:HGNC:47625]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479860","summary":null,"start":151747597,"end":151747700,"strand":-1,"description":"RNA, U6 small nuclear 662, pseudogene [Source:HGNC Symbol;Acc:HGNC:47625]"}, {"versioned_ensembl_gene_id":"ENSG00000253085.1","gene_symbol":"SCARNA11","gene_name":"Small Cajal body specific RNA 11 [Source:RFAM;Acc:RF00564]","synonyms":"ACA57","biotype":"scaRNA","ncbi_id":"677780","summary":null,"start":13696070,"end":13696199,"strand":-1,"description":"Small Cajal body specific RNA 11 [Source:RFAM;Acc:RF00564]"}, {"versioned_ensembl_gene_id":"ENSG00000252029.1","gene_symbol":"RNA5SP253","gene_name":"RNA, 5S ribosomal pseudogene 253 [Source:HGNC Symbol;Acc:HGNC:43153]","synonyms":"RN5S253","biotype":"rRNA","ncbi_id":"106480760","summary":null,"start":12087396,"end":12087445,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 253 [Source:HGNC Symbol;Acc:HGNC:43153]"}, {"versioned_ensembl_gene_id":"ENSG00000221601.1","gene_symbol":"RNU4ATAC2P","gene_name":"RNA, U4atac small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:39003]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873889","summary":null,"start":159318042,"end":159318167,"strand":1,"description":"RNA, U4atac small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:39003]"}, {"versioned_ensembl_gene_id":"ENSG00000252723.2","gene_symbol":"RNU6-677P","gene_name":"RNA, U6 small nuclear 677, pseudogene [Source:HGNC Symbol;Acc:HGNC:47640]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481395","summary":null,"start":37333857,"end":37333957,"strand":-1,"description":"RNA, U6 small nuclear 677, pseudogene [Source:HGNC Symbol;Acc:HGNC:47640]"}, {"versioned_ensembl_gene_id":"ENSG00000200138.1","gene_symbol":"RNY1P10","gene_name":"RNA, Ro-associated Y1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:50873]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480308","summary":null,"start":28183318,"end":28183430,"strand":1,"description":"RNA, Ro-associated Y1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:50873]"}, {"versioned_ensembl_gene_id":"ENSG00000221806.1","gene_symbol":"RNU6ATAC34P","gene_name":"RNA, U6atac small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46933]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479557","summary":null,"start":18611047,"end":18611167,"strand":-1,"description":"RNA, U6atac small nuclear 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:46933]"}, {"versioned_ensembl_gene_id":"ENSG00000263879.1","gene_symbol":"SNORA38","gene_name":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]","synonyms":"ACA38,ACA38","biotype":"snoRNA","ncbi_id":"677820","summary":null,"start":31610483,"end":31610614,"strand":1,"description":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]"}, {"versioned_ensembl_gene_id":"ENSG00000284324.1","gene_symbol":"MIR3175","gene_name":"microRNA 3175 [Source:HGNC Symbol;Acc:HGNC:38299]","synonyms":"hsa-mir-3175","biotype":"miRNA","ncbi_id":"100422995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":92904399,"end":92904475,"strand":1,"description":"microRNA 3175 [Source:HGNC Symbol;Acc:HGNC:38299]"}, {"versioned_ensembl_gene_id":"ENSG00000207459.1","gene_symbol":"RNU6-1311P","gene_name":"RNA, U6 small nuclear 1311, pseudogene [Source:HGNC Symbol;Acc:HGNC:48274]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480138","summary":null,"start":134634839,"end":134634945,"strand":-1,"description":"RNA, U6 small nuclear 1311, pseudogene [Source:HGNC Symbol;Acc:HGNC:48274]"}, {"versioned_ensembl_gene_id":"ENSG00000283845.1","gene_symbol":"MIR4721","gene_name":"microRNA 4721 [Source:HGNC Symbol;Acc:HGNC:41609]","synonyms":"hsa-mir-4721","biotype":"miRNA","ncbi_id":"100616256","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28843919,"end":28844007,"strand":-1,"description":"microRNA 4721 [Source:HGNC Symbol;Acc:HGNC:41609]"}, {"versioned_ensembl_gene_id":"ENSG00000206678.1","gene_symbol":"RNU6-144P","gene_name":"RNA, U6 small nuclear 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:47107]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481222","summary":null,"start":137105352,"end":137105458,"strand":1,"description":"RNA, U6 small nuclear 144, pseudogene [Source:HGNC Symbol;Acc:HGNC:47107]"}, {"versioned_ensembl_gene_id":"ENSG00000238719.1","gene_symbol":"RNU7-96P","gene_name":"RNA, U7 small nuclear 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:45630]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480361","summary":null,"start":97913054,"end":97913117,"strand":-1,"description":"RNA, U7 small nuclear 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:45630]"}, {"versioned_ensembl_gene_id":"ENSG00000212358.1","gene_symbol":"RNU6-837P","gene_name":"RNA, U6 small nuclear 837, pseudogene [Source:HGNC Symbol;Acc:HGNC:47800]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479936","summary":null,"start":17071398,"end":17071505,"strand":-1,"description":"RNA, U6 small nuclear 837, pseudogene [Source:HGNC Symbol;Acc:HGNC:47800]"}, {"versioned_ensembl_gene_id":"ENSG00000276760.4","gene_symbol":"AC136352.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136160,"end":167571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238370.1","gene_symbol":"RNU7-103P","gene_name":"RNA, U7 small nuclear 103 pseudogene [Source:HGNC Symbol;Acc:HGNC:45637]","synonyms":null,"biotype":"snRNA","ncbi_id":"107063544","summary":null,"start":589530,"end":589589,"strand":-1,"description":"RNA, U7 small nuclear 103 pseudogene [Source:HGNC Symbol;Acc:HGNC:45637]"}, {"versioned_ensembl_gene_id":"ENSG00000200733.1","gene_symbol":"SNORD38","gene_name":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":89837170,"end":89837237,"strand":1,"description":"Small nucleolar RNA SNORD38 [Source:RFAM;Acc:RF00212]"}, {"versioned_ensembl_gene_id":"ENSG00000212411.1","gene_symbol":"SNORD115","gene_name":"Small nucleolar RNA SNORD115 [Source:RFAM;Acc:RF00105]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":29575306,"end":29575381,"strand":1,"description":"Small nucleolar RNA SNORD115 [Source:RFAM;Acc:RF00105]"}, {"versioned_ensembl_gene_id":"ENSG00000201466.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12760717,"end":12760818,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201395.1","gene_symbol":"RN7SKP257","gene_name":"RNA, 7SK small nuclear pseudogene 257 [Source:HGNC Symbol;Acc:HGNC:45981]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479210","summary":null,"start":36593839,"end":36594147,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 257 [Source:HGNC Symbol;Acc:HGNC:45981]"}, {"versioned_ensembl_gene_id":"ENSG00000253087.1","gene_symbol":"RNU6-1174P","gene_name":"RNA, U6 small nuclear 1174, pseudogene [Source:HGNC Symbol;Acc:HGNC:48137]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481550","summary":null,"start":134780527,"end":134780627,"strand":-1,"description":"RNA, U6 small nuclear 1174, pseudogene [Source:HGNC Symbol;Acc:HGNC:48137]"}, {"versioned_ensembl_gene_id":"ENSG00000270384.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":145431527,"end":145431693,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000266689.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32510948,"end":32511094,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000283904.1","gene_symbol":"MIR155","gene_name":"microRNA 155 [Source:HGNC Symbol;Acc:HGNC:31542]","synonyms":"MIRN155,hsa-mir-155","biotype":"miRNA","ncbi_id":"406947","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25573980,"end":25574044,"strand":1,"description":"microRNA 155 [Source:HGNC Symbol;Acc:HGNC:31542]"}, {"versioned_ensembl_gene_id":"ENSG00000207799.1","gene_symbol":"MIR520G","gene_name":"microRNA 520g [Source:HGNC Symbol;Acc:HGNC:32116]","synonyms":"MIRN520G,hsa-mir-520g","biotype":"miRNA","ncbi_id":"574484","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53722166,"end":53722255,"strand":1,"description":"microRNA 520g [Source:HGNC Symbol;Acc:HGNC:32116]"}, {"versioned_ensembl_gene_id":"ENSG00000252621.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37303000,"end":37303109,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000184502.3","gene_symbol":"GAST","gene_name":"gastrin [Source:HGNC Symbol;Acc:HGNC:4164]","synonyms":"GAS","biotype":"protein_coding","ncbi_id":"2520","summary":"Gastrin is a hormone whose main function is to stimulate secretion of hydrochloric acid by the gastric mucosa, which results in gastrin formation inhibition. This hormone also acts as a mitogenic factor for gastrointestinal epithelial cells. Gastrin has two biologically active peptide forms, G34 and G17. [provided by RefSeq, Jul 2008]","start":41712326,"end":41715969,"strand":1,"description":"gastrin [Source:HGNC Symbol;Acc:HGNC:4164]"}, {"versioned_ensembl_gene_id":"ENSG00000266148.1","gene_symbol":"MIR5583-1","gene_name":"microRNA 5583-1 [Source:HGNC Symbol;Acc:HGNC:43491]","synonyms":"hsa-mir-5583-1","biotype":"miRNA","ncbi_id":"100847025","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39676721,"end":39676779,"strand":1,"description":"microRNA 5583-1 [Source:HGNC Symbol;Acc:HGNC:43491]"}, {"versioned_ensembl_gene_id":"ENSG00000200079.1","gene_symbol":"RNA5SP326","gene_name":"RNA, 5S ribosomal pseudogene 326 [Source:HGNC Symbol;Acc:HGNC:43226]","synonyms":"RN5S326","biotype":"rRNA","ncbi_id":"100873592","summary":null,"start":107461560,"end":107461669,"strand":1,"description":"RNA, 5S ribosomal pseudogene 326 [Source:HGNC Symbol;Acc:HGNC:43226]"}, {"versioned_ensembl_gene_id":"ENSG00000212242.1","gene_symbol":"RNA5SP219","gene_name":"RNA, 5S ribosomal pseudogene 219 [Source:HGNC Symbol;Acc:HGNC:43119]","synonyms":"RN5S219","biotype":"rRNA","ncbi_id":"100873479","summary":null,"start":136630243,"end":136630355,"strand":1,"description":"RNA, 5S ribosomal pseudogene 219 [Source:HGNC Symbol;Acc:HGNC:43119]"}, {"versioned_ensembl_gene_id":"ENSG00000265395.1","gene_symbol":"MIR3944","gene_name":"microRNA 3944 [Source:HGNC Symbol;Acc:HGNC:38898]","synonyms":"hsa-mir-3944","biotype":"miRNA","ncbi_id":"100500911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133371556,"end":133371663,"strand":-1,"description":"microRNA 3944 [Source:HGNC Symbol;Acc:HGNC:38898]"}, {"versioned_ensembl_gene_id":"ENSG00000251857.1","gene_symbol":"RNA5SP362","gene_name":"RNA, 5S ribosomal pseudogene 362 [Source:HGNC Symbol;Acc:HGNC:43262]","synonyms":"RN5S362","biotype":"rRNA","ncbi_id":"100873621","summary":null,"start":66066221,"end":66066338,"strand":1,"description":"RNA, 5S ribosomal pseudogene 362 [Source:HGNC Symbol;Acc:HGNC:43262]"}, {"versioned_ensembl_gene_id":"ENSG00000275680.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58951185,"end":58951513,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202461.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12024012,"end":12024124,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242483.3","gene_symbol":"RN7SL293P","gene_name":"RNA, 7SL, cytoplasmic 293, pseudogene [Source:HGNC Symbol;Acc:HGNC:46309]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481835","summary":null,"start":11379395,"end":11379675,"strand":1,"description":"RNA, 7SL, cytoplasmic 293, pseudogene [Source:HGNC Symbol;Acc:HGNC:46309]"}, {"versioned_ensembl_gene_id":"ENSG00000201209.1","gene_symbol":"SNORD42","gene_name":"Small nucleolar RNA SNORD42 [Source:RFAM;Acc:RF00150]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":28232756,"end":28232823,"strand":-1,"description":"Small nucleolar RNA SNORD42 [Source:RFAM;Acc:RF00150]"}, {"versioned_ensembl_gene_id":"ENSG00000283762.1","gene_symbol":"MIR20A","gene_name":"microRNA 20a [Source:HGNC Symbol;Acc:HGNC:31577]","synonyms":"MIRN20A,MIRN20,hsa-mir-20a,hsa-mir-20","biotype":"miRNA","ncbi_id":"406982","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91351065,"end":91351135,"strand":1,"description":"microRNA 20a [Source:HGNC Symbol;Acc:HGNC:31577]"}, {"versioned_ensembl_gene_id":"ENSG00000241225.2","gene_symbol":"NMTRS-TGA3-1","gene_name":"nuclear-encoded mitochondrial transfer RNA-Ser (TGA) 3-1 [Source:HGNC Symbol;Acc:HGNC:35087]","synonyms":"TRNAS30P","biotype":"unprocessed_pseudogene","ncbi_id":"100189512","summary":null,"start":22528853,"end":22528921,"strand":-1,"description":"nuclear-encoded mitochondrial transfer RNA-Ser (TGA) 3-1 [Source:HGNC Symbol;Acc:HGNC:35087]"}, {"versioned_ensembl_gene_id":"ENSG00000243655.2","gene_symbol":"AC132825.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22524563,"end":22525330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263725.1","gene_symbol":"AC138761.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22221221,"end":22221605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263563.5","gene_symbol":"UBBP4","gene_name":"ubiquitin B pseudogene 4 [Source:NCBI gene;Acc:23666]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"23666","summary":null,"start":22202995,"end":22205154,"strand":1,"description":"ubiquitin B pseudogene 4 [Source:NCBI gene;Acc:23666]"}, {"versioned_ensembl_gene_id":"ENSG00000165527.6","gene_symbol":"ARF6","gene_name":"ADP ribosylation factor 6 [Source:HGNC Symbol;Acc:HGNC:659]","synonyms":null,"biotype":"protein_coding","ncbi_id":"382","summary":"This gene encodes a member of the human ARF gene family, which is part of the RAS superfamily. The ARF genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The product of this gene is localized to the plasma membrane, and regulates vesicular trafficking, remodelling of membrane lipids, and signaling pathways that lead to actin remodeling. A pseudogene of this gene is located on chromosome 7. [provided by RefSeq, Jul 2008]","start":49893092,"end":49897054,"strand":1,"description":"ADP ribosylation factor 6 [Source:HGNC Symbol;Acc:HGNC:659]"}, {"versioned_ensembl_gene_id":"ENSG00000266050.2","gene_symbol":"AC233702.7","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":21566569,"end":21574517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169169.14","gene_symbol":"CPT1C","gene_name":"carnitine palmitoyltransferase 1C [Source:HGNC Symbol;Acc:HGNC:18540]","synonyms":"FLJ23809,CPTIC,CPT1P","biotype":"protein_coding","ncbi_id":"126129","summary":"This gene encodes a member of the carnitine/choline acetyltransferase family. The encoded protein regulates the beta-oxidation and transport of long-chain fatty acids into mitochondria, and may play a role in the regulation of feeding behavior and whole-body energy homeostasis. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":49690898,"end":49713731,"strand":1,"description":"carnitine palmitoyltransferase 1C [Source:HGNC Symbol;Acc:HGNC:18540]"}, {"versioned_ensembl_gene_id":"ENSG00000173715.15","gene_symbol":"C11orf80","gene_name":"chromosome 11 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:26197]","synonyms":"TOPOVIBL,FLJ22531","biotype":"protein_coding","ncbi_id":"79703","summary":null,"start":66744451,"end":66843328,"strand":1,"description":"chromosome 11 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:26197]"}, {"versioned_ensembl_gene_id":"ENSG00000256091.1","gene_symbol":"MTRF1LP1","gene_name":"mitochondrial translational release factor 1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132520","summary":null,"start":113711720,"end":113712398,"strand":1,"description":"mitochondrial translational release factor 1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50611]"}, {"versioned_ensembl_gene_id":"ENSG00000005961.17","gene_symbol":"ITGA2B","gene_name":"integrin subunit alpha 2b [Source:HGNC Symbol;Acc:HGNC:6138]","synonyms":"GP2B,CD41B,CD41,PPP1R93","biotype":"protein_coding","ncbi_id":"3674","summary":"This gene encodes a member of the integrin alpha chain family of proteins. The encoded preproprotein is proteolytically processed to generate light and heavy chains that associate through disulfide linkages to form a subunit of the alpha-IIb/beta-3 integrin cell adhesion receptor. This receptor plays a crucial role in the blood coagulation system, by mediating platelet aggregation. Mutations in this gene are associated with platelet-type bleeding disorders, which are characterized by a failure of platelet aggregation, including Glanzmann thrombasthenia. [provided by RefSeq, Jan 2016]","start":44372180,"end":44389505,"strand":-1,"description":"integrin subunit alpha 2b [Source:HGNC Symbol;Acc:HGNC:6138]"}, {"versioned_ensembl_gene_id":"ENSG00000236801.1","gene_symbol":"RPL24P8","gene_name":"ribosomal protein L24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36409]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270964","summary":null,"start":70217195,"end":70217668,"strand":1,"description":"ribosomal protein L24 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36409]"}, {"versioned_ensembl_gene_id":"ENSG00000165072.9","gene_symbol":"MAMDC2","gene_name":"MAM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23673]","synonyms":"MGC21981","biotype":"protein_coding","ncbi_id":"256691","summary":null,"start":70043581,"end":70226970,"strand":1,"description":"MAM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23673]"}, {"versioned_ensembl_gene_id":"ENSG00000140107.10","gene_symbol":"SLC25A47","gene_name":"solute carrier family 25 member 47 [Source:HGNC Symbol;Acc:HGNC:20115]","synonyms":"C14orf68","biotype":"protein_coding","ncbi_id":"283600","summary":"This gene encodes a member of a large family of mitochondrial transporters. The nuclear-encoded carrier protein is embedded in the inner mitochondrial membrane. This member of the family is thought to be an uncoupling protein that uncouples mitochondrial respiration from ATP synthesis by dissipating the transmembrane proton gradient. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":100323337,"end":100330378,"strand":1,"description":"solute carrier family 25 member 47 [Source:HGNC Symbol;Acc:HGNC:20115]"}, {"versioned_ensembl_gene_id":"ENSG00000225522.2","gene_symbol":"AL592114.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204183006,"end":204183537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188647.12","gene_symbol":"PTAR1","gene_name":"protein prenyltransferase alpha subunit repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:30449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"375743","summary":null,"start":69709522,"end":69759959,"strand":-1,"description":"protein prenyltransferase alpha subunit repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:30449]"}, {"versioned_ensembl_gene_id":"ENSG00000100811.12","gene_symbol":"YY1","gene_name":"YY1 transcription factor [Source:HGNC Symbol;Acc:HGNC:12856]","synonyms":"YIN-YANG-1,UCRBP,NF-E1,INO80S,DELTA","biotype":"protein_coding","ncbi_id":"7528","summary":"YY1 is a ubiquitously distributed transcription factor belonging to the GLI-Kruppel class of zinc finger proteins. The protein is involved in repressing and activating a diverse number of promoters. YY1 may direct histone deacetylases and histone acetyltransferases to a promoter in order to activate or repress the promoter, thus implicating histone modification in the function of YY1. [provided by RefSeq, Jul 2008]","start":100238298,"end":100282792,"strand":1,"description":"YY1 transcription factor [Source:HGNC Symbol;Acc:HGNC:12856]"}, {"versioned_ensembl_gene_id":"ENSG00000259052.1","gene_symbol":"AL157871.6","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":100279959,"end":100291456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261447.1","gene_symbol":"AL162412.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69672749,"end":69673713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178307.9","gene_symbol":"TMEM11","gene_name":"transmembrane protein 11 [Source:HGNC Symbol;Acc:HGNC:16823]","synonyms":"C17orf35,PMI,PM1","biotype":"protein_coding","ncbi_id":"8834","summary":null,"start":21197280,"end":21214624,"strand":-1,"description":"transmembrane protein 11 [Source:HGNC Symbol;Acc:HGNC:16823]"}, {"versioned_ensembl_gene_id":"ENSG00000143842.14","gene_symbol":"SOX13","gene_name":"SRY-box 13 [Source:HGNC Symbol;Acc:HGNC:11192]","synonyms":"Sox-13,MGC117216,ICA12","biotype":"protein_coding","ncbi_id":"9580","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. It has also been determined to be a type-1 diabetes autoantigen, also known as islet cell antibody 12. [provided by RefSeq, Jul 2008]","start":204073115,"end":204127743,"strand":1,"description":"SRY-box 13 [Source:HGNC Symbol;Acc:HGNC:11192]"}, {"versioned_ensembl_gene_id":"ENSG00000159714.10","gene_symbol":"ZDHHC1","gene_name":"zinc finger DHHC-type containing 1 [Source:HGNC Symbol;Acc:HGNC:17916]","synonyms":"C16orf1,ZNF377,HSU90653","biotype":"protein_coding","ncbi_id":"29800","summary":null,"start":67394419,"end":67416833,"strand":-1,"description":"zinc finger DHHC-type containing 1 [Source:HGNC Symbol;Acc:HGNC:17916]"}, {"versioned_ensembl_gene_id":"ENSG00000205976.4","gene_symbol":"AC091951.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7299774,"end":7306592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249734.1","gene_symbol":"LINC02236","gene_name":"long intergenic non-protein coding RNA 2236 [Source:HGNC Symbol;Acc:HGNC:53107]","synonyms":"RP11-332J15.1","biotype":"lincRNA","ncbi_id":"109729133","summary":null,"start":6795880,"end":6826728,"strand":1,"description":"long intergenic non-protein coding RNA 2236 [Source:HGNC Symbol;Acc:HGNC:53107]"}, {"versioned_ensembl_gene_id":"ENSG00000187867.8","gene_symbol":"PALM3","gene_name":"paralemmin 3 [Source:HGNC Symbol;Acc:HGNC:33274]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342979","summary":null,"start":14053365,"end":14059159,"strand":-1,"description":"paralemmin 3 [Source:HGNC Symbol;Acc:HGNC:33274]"}, {"versioned_ensembl_gene_id":"ENSG00000256223.5","gene_symbol":"ZNF10","gene_name":"zinc finger protein 10 [Source:HGNC Symbol;Acc:HGNC:12879]","synonyms":"KOX1","biotype":"protein_coding","ncbi_id":"7556","summary":"The protein encoded by this gene contains a C2H2 zinc finger, and has been shown to function as a transcriptional repressor. The Kruppel-associated box (KRAB) domain of this protein is found to be responsible for its transcriptional repression activity. RING finger containing protein TIF1 was reported to interact with the KRAB domain, and may serve as a mediator for the repression activity of this protein. [provided by RefSeq, Jul 2008]","start":133130575,"end":133159465,"strand":1,"description":"zinc finger protein 10 [Source:HGNC Symbol;Acc:HGNC:12879]"}, {"versioned_ensembl_gene_id":"ENSG00000169689.14","gene_symbol":"CENPX","gene_name":"centromere protein X [Source:HGNC Symbol;Acc:HGNC:11422]","synonyms":"STRA13,MHF2,MGC14480,FAAP10,CENP-X","biotype":"protein_coding","ncbi_id":"201254","summary":null,"start":82018702,"end":82024107,"strand":-1,"description":"centromere protein X [Source:HGNC Symbol;Acc:HGNC:11422]"}, {"versioned_ensembl_gene_id":"ENSG00000104998.3","gene_symbol":"IL27RA","gene_name":"interleukin 27 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:17290]","synonyms":"zcytor1,WSX1,WSX-1,TCCR,IL-27R,CRL1","biotype":"protein_coding","ncbi_id":"9466","summary":"In mice, CD4+ helper T-cells differentiate into type 1 (Th1) cells, which are critical for cell-mediated immunity, predominantly under the influence of IL12. Also, IL4 influences their differentiation into type 2 (Th2) cells, which are critical for most antibody responses. Mice deficient in these cytokines, their receptors, or associated transcription factors have impaired, but are not absent of, Th1 or Th2 immune responses. This gene encodes a protein which is similar to the mouse T-cell cytokine receptor Tccr at the amino acid level, and is predicted to be a glycosylated transmembrane protein. [provided by RefSeq, Jul 2008]","start":14031748,"end":14053216,"strand":1,"description":"interleukin 27 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:17290]"}, {"versioned_ensembl_gene_id":"ENSG00000169696.15","gene_symbol":"ASPSCR1","gene_name":"ASPSCR1, UBX domain containing tether for SLC2A4 [Source:HGNC Symbol;Acc:HGNC:13825]","synonyms":"UBXN9,UBXD9,TUG,ASPS,ASPL","biotype":"protein_coding","ncbi_id":"79058","summary":"The protein encoded by this gene contains a UBX domain and interacts with glucose transporter type 4 (GLUT4). This protein is a tether, which sequesters the GLUT4 in intracellular vesicles in muscle and fat cells in the absence of insulin, and redistributes the GLUT4 to the plasma membrane within minutes of insulin stimulation. Translocation t(X;17)(p11;q25) of this gene with transcription factor TFE3 gene results in a ASPSCR1-TFE3 fusion protein in alveolar soft part sarcoma and in renal cell carcinomas. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Oct 2011]","start":81976807,"end":82017406,"strand":1,"description":"ASPSCR1, UBX domain containing tether for SLC2A4 [Source:HGNC Symbol;Acc:HGNC:13825]"}, {"versioned_ensembl_gene_id":"ENSG00000264735.1","gene_symbol":"AC145207.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81965632,"end":81966589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264125.1","gene_symbol":"AC104984.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30204318,"end":30206468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172992.11","gene_symbol":"DCAKD","gene_name":"dephospho-CoA kinase domain containing [Source:HGNC Symbol;Acc:HGNC:26238]","synonyms":"FLJ22955","biotype":"protein_coding","ncbi_id":"79877","summary":null,"start":45023340,"end":45061109,"strand":-1,"description":"dephospho-CoA kinase domain containing [Source:HGNC Symbol;Acc:HGNC:26238]"}, {"versioned_ensembl_gene_id":"ENSG00000203722.7","gene_symbol":"RAET1G","gene_name":"retinoic acid early transcript 1G [Source:HGNC Symbol;Acc:HGNC:16795]","synonyms":"ULBP5","biotype":"protein_coding","ncbi_id":"353091","summary":"This gene encodes a member of the major histocompatibility complex (MHC) class I family of proteins. Although the encoded protein includes C-terminal transmembrane and cytoplasmic domains, proteolytic processing results in the removal of these domains and subsequent tethering to the plasma membrane by a glycosylphosphatidylinositol (GPI)-anchor. The encoded protein is one of several related ligands of the natural killer group 2, member D (NKG2D) receptor, which functions as an activating receptor in innate and adaptive immunity. This gene is present in a gene cluster on chromosome 6. [provided by RefSeq, Jul 2015]","start":149916878,"end":149923121,"strand":-1,"description":"retinoic acid early transcript 1G [Source:HGNC Symbol;Acc:HGNC:16795]"}, {"versioned_ensembl_gene_id":"ENSG00000131503.20","gene_symbol":"ANKHD1","gene_name":"ankyrin repeat and KH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24714]","synonyms":"MASK1,MASK,KIAA1085,FLJ20288,FLJ14127,FLJ11979,FLJ10042","biotype":"protein_coding","ncbi_id":"54882","summary":"This gene encodes a protein with multiple ankyrin repeat domains and a single KH-domain. The protein is thought to function as a scaffolding protein, and it may be involved in the regulation of caspases and thereby play an antiapoptotic role in cell survival. Alternative splicing results in multiple transcript variants, one of which generates a fusion transcript (MASK-BP3) with the downstream eIF4E-binding protein 3 (EIF4EBP3) gene, resulting in a protein comprised of the ANKHD1 sequence for the majority of the protein and a different C-terminus due to an alternate reading frame for the EIF4EBP3 segments. [provided by RefSeq, Sep 2010]","start":140401814,"end":140539856,"strand":1,"description":"ankyrin repeat and KH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24714]"}, {"versioned_ensembl_gene_id":"ENSG00000187870.7","gene_symbol":"RNFT1P3","gene_name":"ring finger protein, transmembrane 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44389]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101929203","summary":null,"start":20743333,"end":20754501,"strand":-1,"description":"ring finger protein, transmembrane 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44389]"}, {"versioned_ensembl_gene_id":"ENSG00000237761.1","gene_symbol":"AL161646.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104616102,"end":104616973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228696.8","gene_symbol":"ARL17B","gene_name":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]","synonyms":"ARL17","biotype":"protein_coding","ncbi_id":"100506084","summary":null,"start":46274784,"end":46361797,"strand":-1,"description":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]"}, {"versioned_ensembl_gene_id":"ENSG00000258383.1","gene_symbol":"AL132819.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99324799,"end":99332015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235546.2","gene_symbol":"AC087499.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20612667,"end":20614008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227685.1","gene_symbol":"LINC02088","gene_name":"long intergenic non-protein coding RNA 2088 [Source:HGNC Symbol;Acc:HGNC:52939]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371582","summary":null,"start":20612912,"end":20633234,"strand":-1,"description":"long intergenic non-protein coding RNA 2088 [Source:HGNC Symbol;Acc:HGNC:52939]"}, {"versioned_ensembl_gene_id":"ENSG00000232889.2","gene_symbol":"AC087499.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20595531,"end":20595708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258795.1","gene_symbol":"AL132719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98497132,"end":98514798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259026.1","gene_symbol":"AL049833.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97110416,"end":97119247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228261.1","gene_symbol":"AL162742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104323369,"end":104327004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258393.1","gene_symbol":"AL049833.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97116355,"end":97121501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244053.1","gene_symbol":"AL157792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47200575,"end":47201104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215218.3","gene_symbol":"UBE2QL1","gene_name":"ubiquitin conjugating enzyme E2 Q family like 1 [Source:HGNC Symbol;Acc:HGNC:37269]","synonyms":"FLJ25076","biotype":"protein_coding","ncbi_id":"134111","summary":null,"start":6448623,"end":6494909,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q family like 1 [Source:HGNC Symbol;Acc:HGNC:37269]"}, {"versioned_ensembl_gene_id":"ENSG00000181523.12","gene_symbol":"SGSH","gene_name":"N-sulfoglucosamine sulfohydrolase [Source:HGNC Symbol;Acc:HGNC:10818]","synonyms":"SFMD,MPS3A,HSS","biotype":"protein_coding","ncbi_id":"6448","summary":"This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jun 2017]","start":80206716,"end":80220923,"strand":-1,"description":"N-sulfoglucosamine sulfohydrolase [Source:HGNC Symbol;Acc:HGNC:10818]"}, {"versioned_ensembl_gene_id":"ENSG00000233806.7","gene_symbol":"LINC01237","gene_name":"long intergenic non-protein coding RNA 1237 [Source:HGNC Symbol;Acc:HGNC:49793]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101927289","summary":null,"start":241881363,"end":242078722,"strand":1,"description":"long intergenic non-protein coding RNA 1237 [Source:HGNC Symbol;Acc:HGNC:49793]"}, {"versioned_ensembl_gene_id":"ENSG00000138162.18","gene_symbol":"TACC2","gene_name":"transforming acidic coiled-coil containing protein 2 [Source:HGNC Symbol;Acc:HGNC:11523]","synonyms":"AZU-1","biotype":"protein_coding","ncbi_id":"10579","summary":"Transforming acidic coiled-coil proteins are a conserved family of centrosome- and microtubule-interacting proteins that are implicated in cancer. This gene encodes a protein that concentrates at centrosomes throughout the cell cycle. This gene lies within a chromosomal region associated with tumorigenesis. Expression of this gene is induced by erythropoietin and is thought to affect the progression of breast tumors. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":121989174,"end":122254545,"strand":1,"description":"transforming acidic coiled-coil containing protein 2 [Source:HGNC Symbol;Acc:HGNC:11523]"}, {"versioned_ensembl_gene_id":"ENSG00000141527.16","gene_symbol":"CARD14","gene_name":"caspase recruitment domain family member 14 [Source:HGNC Symbol;Acc:HGNC:16446]","synonyms":"PSORS2,CARMA2,BIMP2","biotype":"protein_coding","ncbi_id":"79092","summary":"This gene encodes a caspase recruitment domain-containing protein that is a member of the membrane-associated guanylate kinase (MAGUK) family of proteins. Members of this protein family are scaffold proteins that are involved in a diverse array of cellular processes including cellular adhesion, signal transduction and cell polarity control. This protein has been shown to specifically interact with BCL10, a protein known to function as a positive regulator of cell apoptosis and NF-kappaB activation. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]","start":80169992,"end":80209331,"strand":1,"description":"caspase recruitment domain family member 14 [Source:HGNC Symbol;Acc:HGNC:16446]"}, {"versioned_ensembl_gene_id":"ENSG00000196155.12","gene_symbol":"PLEKHG4","gene_name":"pleckstrin homology and RhoGEF domain containing G4 [Source:HGNC Symbol;Acc:HGNC:24501]","synonyms":"SCA4,DKFZP434I216,ARHGEF44","biotype":"protein_coding","ncbi_id":"25894","summary":"The protein encoded by this gene can function as a guanine nucleotide exchange factor (GEF) and may play a role in intracellular signaling and cytoskeleton dynamics at the Golgi apparatus. Polymorphisms in the region of this gene have been found to be associated with spinocerebellar ataxia in some study populations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":67277510,"end":67289499,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G4 [Source:HGNC Symbol;Acc:HGNC:24501]"}, {"versioned_ensembl_gene_id":"ENSG00000258616.5","gene_symbol":"LINC02303","gene_name":"long intergenic non-protein coding RNA 2303 [Source:HGNC Symbol;Acc:HGNC:53222]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370479","summary":null,"start":45706250,"end":45715952,"strand":-1,"description":"long intergenic non-protein coding RNA 2303 [Source:HGNC Symbol;Acc:HGNC:53222]"}, {"versioned_ensembl_gene_id":"ENSG00000226544.4","gene_symbol":"RPL7P22","gene_name":"ribosomal protein L7 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728620","summary":null,"start":72725419,"end":72726151,"strand":1,"description":"ribosomal protein L7 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35802]"}, {"versioned_ensembl_gene_id":"ENSG00000261586.2","gene_symbol":"AC068987.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51817899,"end":51820150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268669.1","gene_symbol":"AC008687.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49042174,"end":49042731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255277.3","gene_symbol":"ABCC6P2","gene_name":"ATP binding cassette subfamily C member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33353]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"730013","summary":null,"start":14820792,"end":14824702,"strand":-1,"description":"ATP binding cassette subfamily C member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33353]"}, {"versioned_ensembl_gene_id":"ENSG00000187239.16","gene_symbol":"FNBP1","gene_name":"formin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17069]","synonyms":"KIAA0554,FBP17","biotype":"protein_coding","ncbi_id":"23048","summary":"The protein encoded by this gene is a member of the formin-binding-protein family. The protein contains an N-terminal Fer/Cdc42-interacting protein 4 (CIP4) homology (FCH) domain followed by a coiled-coil domain, a proline-rich motif, a second coiled-coil domain, a Rho family protein-binding domain (RBD), and a C-terminal SH3 domain. This protein binds sorting nexin 2 (SNX2), tankyrase (TNKS), and dynamin; an interaction between this protein and formin has not been demonstrated yet in human. [provided by RefSeq, Jul 2008]","start":129887187,"end":130043194,"strand":-1,"description":"formin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17069]"}, {"versioned_ensembl_gene_id":"ENSG00000261978.1","gene_symbol":"AC116025.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80023894,"end":80026107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126262.4","gene_symbol":"FFAR2","gene_name":"free fatty acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:4501]","synonyms":"GPR43,FFA2R","biotype":"protein_coding","ncbi_id":"2867","summary":"This gene encodes a member of the GP40 family of G protein-coupled receptors that are clustered together on chromosome 19. The encoded protein is a receptor for short chain free fatty acids and may be involved in the inflammatory response and in regulating lipid plasma levels. [provided by RefSeq, Apr 2009]","start":35443907,"end":35451767,"strand":1,"description":"free fatty acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:4501]"}, {"versioned_ensembl_gene_id":"ENSG00000227741.1","gene_symbol":"AL121987.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160202199,"end":160208869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283479.1","gene_symbol":"AC002511.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35407770,"end":35408493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104957.13","gene_symbol":"CCDC130","gene_name":"coiled-coil domain containing 130 [Source:HGNC Symbol;Acc:HGNC:28118]","synonyms":"MGC10471","biotype":"protein_coding","ncbi_id":"81576","summary":null,"start":13731760,"end":13763296,"strand":1,"description":"coiled-coil domain containing 130 [Source:HGNC Symbol;Acc:HGNC:28118]"}, {"versioned_ensembl_gene_id":"ENSG00000265096.1","gene_symbol":"C1QTNF1-AS1","gene_name":"C1QTNF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44351]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507410","summary":null,"start":79019209,"end":79027655,"strand":-1,"description":"C1QTNF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44351]"}, {"versioned_ensembl_gene_id":"ENSG00000184898.6","gene_symbol":"RBM43","gene_name":"RNA binding motif protein 43 [Source:HGNC Symbol;Acc:HGNC:24790]","synonyms":"FLJ45645,C2orf38","biotype":"protein_coding","ncbi_id":"375287","summary":null,"start":151247940,"end":151261879,"strand":-1,"description":"RNA binding motif protein 43 [Source:HGNC Symbol;Acc:HGNC:24790]"}, {"versioned_ensembl_gene_id":"ENSG00000273729.1","gene_symbol":"AC007686.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77028086,"end":77031572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119669.4","gene_symbol":"IRF2BPL","gene_name":"interferon regulatory factor 2 binding protein like [Source:HGNC Symbol;Acc:HGNC:14282]","synonyms":"C14orf4,KIAA1865,EAP1","biotype":"protein_coding","ncbi_id":"64207","summary":"This gene encodes a transcription factor that may play a role in regulating female reproductive function. [provided by RefSeq, Jun 2012]","start":77024543,"end":77028699,"strand":-1,"description":"interferon regulatory factor 2 binding protein like [Source:HGNC Symbol;Acc:HGNC:14282]"}, {"versioned_ensembl_gene_id":"ENSG00000055130.15","gene_symbol":"CUL1","gene_name":"cullin 1 [Source:HGNC Symbol;Acc:HGNC:2551]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8454","summary":null,"start":148697914,"end":148801036,"strand":1,"description":"cullin 1 [Source:HGNC Symbol;Acc:HGNC:2551]"}, {"versioned_ensembl_gene_id":"ENSG00000204429.4","gene_symbol":"AL451142.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88180673,"end":88181447,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276535.1","gene_symbol":"AL353726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88144851,"end":88145850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131508.15","gene_symbol":"UBE2D2","gene_name":"ubiquitin conjugating enzyme E2 D2 [Source:HGNC Symbol;Acc:HGNC:12475]","synonyms":"UBC4,UbcH5B","biotype":"protein_coding","ncbi_id":"7322","summary":"Regulated degradation of misfolded, damaged or short-lived proteins in eukaryotes occurs via the ubiquitin (Ub)-proteasome system (UPS). An integral part of the UPS system is the ubiquitination of target proteins and covalent linkage of Ub-containing proteins to form polymeric chains, marking them as targets for 26S proteasome-mediated degradation. Ubiquitination of proteins is mediated by a cascade of enzymes which includes E1 (ubiquitin activating), E2 (ubiquitin conjugating), and E3 (ubiquitin ligases) enzymes. This gene encodes a member of the E2 enzyme family. Substrates of this enzyme include the tumor suppressor protein p53 and peroxisomal biogenesis factor 5 (PEX5). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":139526431,"end":139628433,"strand":1,"description":"ubiquitin conjugating enzyme E2 D2 [Source:HGNC Symbol;Acc:HGNC:12475]"}, {"versioned_ensembl_gene_id":"ENSG00000236304.1","gene_symbol":"AP001189.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76657056,"end":76663866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232959.1","gene_symbol":"AL356475.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170024077,"end":170024683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013523.9","gene_symbol":"ANGEL1","gene_name":"angel homolog 1 [Source:HGNC Symbol;Acc:HGNC:19961]","synonyms":"KIAA0759,Ccr4e","biotype":"protein_coding","ncbi_id":"23357","summary":null,"start":76786178,"end":76826246,"strand":-1,"description":"angel homolog 1 [Source:HGNC Symbol;Acc:HGNC:19961]"}, {"versioned_ensembl_gene_id":"ENSG00000273186.1","gene_symbol":"AL359091.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":128431598,"end":128432006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235378.2","gene_symbol":"MRPS10P1","gene_name":"mitochondrial ribosomal protein S10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29728]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359753","summary":null,"start":169990067,"end":169990196,"strand":1,"description":"mitochondrial ribosomal protein S10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29728]"}, {"versioned_ensembl_gene_id":"ENSG00000255562.2","gene_symbol":"UNC93B6","gene_name":"unc-93 homolog B6 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:34053]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"255620","summary":null,"start":71603260,"end":71608040,"strand":1,"description":"unc-93 homolog B6 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:34053]"}, {"versioned_ensembl_gene_id":"ENSG00000018625.14","gene_symbol":"ATP1A2","gene_name":"ATPase Na+/K+ transporting subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:800]","synonyms":"MHP2,FHM2","biotype":"protein_coding","ncbi_id":"477","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 2 subunit. Mutations in this gene result in familial basilar or hemiplegic migraines, and in a rare syndrome known as alternating hemiplegia of childhood. [provided by RefSeq, Oct 2008]","start":160115759,"end":160143591,"strand":1,"description":"ATPase Na+/K+ transporting subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:800]"}, {"versioned_ensembl_gene_id":"ENSG00000204055.4","gene_symbol":"AL158151.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129176771,"end":129210548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105583.9","gene_symbol":"WDR83OS","gene_name":"WD repeat domain 83 opposite strand [Source:HGNC Symbol;Acc:HGNC:30203]","synonyms":"PTD008,C19orf56","biotype":"protein_coding","ncbi_id":"51398","summary":null,"start":12668071,"end":12671356,"strand":-1,"description":"WD repeat domain 83 opposite strand [Source:HGNC Symbol;Acc:HGNC:30203]"}, {"versioned_ensembl_gene_id":"ENSG00000282408.1","gene_symbol":"AL109920.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106451496,"end":106457248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111961.17","gene_symbol":"SASH1","gene_name":"SAM and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19182]","synonyms":"SH3D6A,KIAA0790,dJ323M4.1","biotype":"protein_coding","ncbi_id":"23328","summary":"This gene encodes a scaffold protein involved in the TLR4 signaling pathway that may stimulate cytokine production and endothelial cell migration in response to invading pathogens. The encoded protein has also been described as a potential tumor suppressor that may negatively regulate proliferation, apoptosis, and invasion of cancer cells, and reduced expression of this gene has been observed in multiple human cancers. Mutations in this gene may be associated with abnormal skin pigmentation in human patients. [provided by RefSeq, Oct 2016]","start":148272304,"end":148552050,"strand":1,"description":"SAM and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19182]"}, {"versioned_ensembl_gene_id":"ENSG00000272593.1","gene_symbol":"AL359091.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128391461,"end":128392016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250496.2","gene_symbol":"ABT1P1","gene_name":"activator of basal transcription 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420695","summary":null,"start":99022311,"end":99023131,"strand":-1,"description":"activator of basal transcription 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39557]"}, {"versioned_ensembl_gene_id":"ENSG00000235268.2","gene_symbol":"KDM4E","gene_name":"lysine demethylase 4E [Source:HGNC Symbol;Acc:HGNC:37098]","synonyms":"KDM5E,KDM4DL,JMJD2E","biotype":"protein_coding","ncbi_id":"390245","summary":"The protein encoded by this intronless gene is a member of a large family of histone lysine demethylases, which use oxygen and 2-oxoglutarate to demethylate di- and trimethylated lys9 of histone H3. Derepression of genes by demethylases is sometimes involved in viral infection or carcinogenesis, so inhibitors of these enzymes are desired. [provided by RefSeq, Dec 2016]","start":95025258,"end":95027596,"strand":1,"description":"lysine demethylase 4E [Source:HGNC Symbol;Acc:HGNC:37098]"}, {"versioned_ensembl_gene_id":"ENSG00000255653.1","gene_symbol":"AP002383.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95011858,"end":95012532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178502.5","gene_symbol":"KLHL11","gene_name":"kelch like family member 11 [Source:HGNC Symbol;Acc:HGNC:19008]","synonyms":"FLJ10572","biotype":"protein_coding","ncbi_id":"55175","summary":null,"start":41853545,"end":41865431,"strand":-1,"description":"kelch like family member 11 [Source:HGNC Symbol;Acc:HGNC:19008]"}, {"versioned_ensembl_gene_id":"ENSG00000259623.1","gene_symbol":"AC125257.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":41848518,"end":41851447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273221.1","gene_symbol":"AL355816.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111184415,"end":111185061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272982.1","gene_symbol":"AL355816.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111181374,"end":111181491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257512.1","gene_symbol":"AC124947.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":93314809,"end":93315941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261775.1","gene_symbol":"AC012435.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74489602,"end":74516959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238007.1","gene_symbol":"AC024619.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29012865,"end":29016512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219547.1","gene_symbol":"AL359715.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80374015,"end":80374569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272129.1","gene_symbol":"AL359715.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80355424,"end":80356859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266504.1","gene_symbol":"AC091132.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45553710,"end":45559070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266918.1","gene_symbol":"AC091132.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45531577,"end":45533838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253303.1","gene_symbol":"IGHVIII-82","gene_name":"immunoglobulin heavy variable (III)-82 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5709]","synonyms":"IGHV(III)-82","biotype":"IG_V_pseudogene","ncbi_id":"28338","summary":null,"start":106879563,"end":106879812,"strand":-1,"description":"immunoglobulin heavy variable (III)-82 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5709]"}, {"versioned_ensembl_gene_id":"ENSG00000253331.1","gene_symbol":"AC008662.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164119098,"end":164234097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100764.13","gene_symbol":"PSMC1","gene_name":"proteasome 26S subunit, ATPase 1 [Source:HGNC Symbol;Acc:HGNC:9547]","synonyms":"S4,p56","biotype":"protein_coding","ncbi_id":"5700","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. This subunit and a 20S core alpha subunit interact specifically with the hepatitis B virus X protein, a protein critical to viral replication. This subunit also interacts with the adenovirus E1A protein and this interaction alters the activity of the proteasome. Finally, this subunit interacts with ataxin-7, suggesting a role for the proteasome in the development of spinocerebellar ataxia type 7, a progressive neurodegenerative disorder. [provided by RefSeq, Jul 2008]","start":90256495,"end":90275429,"strand":1,"description":"proteasome 26S subunit, ATPase 1 [Source:HGNC Symbol;Acc:HGNC:9547]"}, {"versioned_ensembl_gene_id":"ENSG00000249116.1","gene_symbol":"AC025183.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1883966,"end":1884649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186197.13","gene_symbol":"EDARADD","gene_name":"EDAR associated death domain [Source:HGNC Symbol;Acc:HGNC:14341]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128178","summary":"This gene was identified by its association with ectodermal dysplasia, a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands. The protein encoded by this gene is a death domain-containing protein, and is found to interact with EDAR, a death domain receptor known to be required for the development of hair, teeth and other ectodermal derivatives. This protein and EDAR are coexpressed in epithelial cells during the formation of hair follicles and teeth. Through its interaction with EDAR, this protein acts as an adaptor, and links the receptor to downstream signaling pathways. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":236348257,"end":236484914,"strand":1,"description":"EDAR associated death domain [Source:HGNC Symbol;Acc:HGNC:14341]"}, {"versioned_ensembl_gene_id":"ENSG00000256393.1","gene_symbol":"AC138123.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93083598,"end":93083675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248674.1","gene_symbol":"RBBP4P6","gene_name":"RB binding protein 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100820741","summary":null,"start":85190629,"end":85190830,"strand":-1,"description":"RB binding protein 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42373]"}, {"versioned_ensembl_gene_id":"ENSG00000204422.7","gene_symbol":"AL662899.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31686962,"end":31714072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161643.12","gene_symbol":"SIGLEC16","gene_name":"sialic acid binding Ig like lectin 16 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:24851]","synonyms":"SIGLECP16,Siglec-P16","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400709","summary":null,"start":49969673,"end":49975814,"strand":1,"description":"sialic acid binding Ig like lectin 16 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:24851]"}, {"versioned_ensembl_gene_id":"ENSG00000267360.6","gene_symbol":"AC012309.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37093019,"end":37210512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248050.1","gene_symbol":"AC079061.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109644115,"end":109648084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267672.1","gene_symbol":"AC010632.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37091341,"end":37092564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267437.1","gene_symbol":"AC012309.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37128679,"end":37141640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259701.1","gene_symbol":"AC020891.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51278927,"end":51280015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259204.1","gene_symbol":"AC073964.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51064609,"end":51069586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129204.16","gene_symbol":"USP6","gene_name":"ubiquitin specific peptidase 6 [Source:HGNC Symbol;Acc:HGNC:12629]","synonyms":"Tre2,TRE17,Tre-2,HRP1,TRESMCR","biotype":"protein_coding","ncbi_id":"9098","summary":null,"start":5116438,"end":5175034,"strand":1,"description":"ubiquitin specific peptidase 6 [Source:HGNC Symbol;Acc:HGNC:12629]"}, {"versioned_ensembl_gene_id":"ENSG00000119403.13","gene_symbol":"PHF19","gene_name":"PHD finger protein 19 [Source:HGNC Symbol;Acc:HGNC:24566]","synonyms":"TDRD19B,PCL3,MTF2L1,DKFZP727G051","biotype":"protein_coding","ncbi_id":"26147","summary":null,"start":120855652,"end":120894896,"strand":-1,"description":"PHD finger protein 19 [Source:HGNC Symbol;Acc:HGNC:24566]"}, {"versioned_ensembl_gene_id":"ENSG00000234327.7","gene_symbol":"AC012146.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":5111468,"end":5115004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170004.16","gene_symbol":"CHD3","gene_name":"chromodomain helicase DNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:1918]","synonyms":"ZFH,Mi2-ALPHA,Mi-2a","biotype":"protein_coding","ncbi_id":"1107","summary":"This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. This protein is one of the components of a histone deacetylase complex referred to as the Mi-2/NuRD complex which participates in the remodeling of chromatin by deacetylating histones. Chromatin remodeling is essential for many processes including transcription. Autoantibodies against this protein are found in a subset of patients with dermatomyositis. Three alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":7884806,"end":7912760,"strand":1,"description":"chromodomain helicase DNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:1918]"}, {"versioned_ensembl_gene_id":"ENSG00000242488.2","gene_symbol":"AF107885.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":75838157,"end":75839114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162728.4","gene_symbol":"KCNJ9","gene_name":"potassium voltage-gated channel subfamily J member 9 [Source:HGNC Symbol;Acc:HGNC:6270]","synonyms":"Kir3.3,GIRK3","biotype":"protein_coding","ncbi_id":"3765","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. It associates with another G-protein-activated potassium channel to form a heteromultimeric pore-forming complex. [provided by RefSeq, Jul 2008]","start":160081570,"end":160090563,"strand":1,"description":"potassium voltage-gated channel subfamily J member 9 [Source:HGNC Symbol;Acc:HGNC:6270]"}, {"versioned_ensembl_gene_id":"ENSG00000214629.3","gene_symbol":"RPSAP6","gene_name":"ribosomal protein SA pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31458]","synonyms":"LAMR1P6,AC022026.3","biotype":"processed_pseudogene","ncbi_id":"414254","summary":null,"start":74371535,"end":74372416,"strand":1,"description":"ribosomal protein SA pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31458]"}, {"versioned_ensembl_gene_id":"ENSG00000262693.1","gene_symbol":"AC012146.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5075678,"end":5078113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198728.10","gene_symbol":"LDB1","gene_name":"LIM domain binding 1 [Source:HGNC Symbol;Acc:HGNC:6532]","synonyms":"CLIM2,NLI","biotype":"protein_coding","ncbi_id":"8861","summary":null,"start":102107560,"end":102120453,"strand":-1,"description":"LIM domain binding 1 [Source:HGNC Symbol;Acc:HGNC:6532]"}, {"versioned_ensembl_gene_id":"ENSG00000142025.15","gene_symbol":"DMRTC2","gene_name":"DMRT like family C2 [Source:HGNC Symbol;Acc:HGNC:13911]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63946","summary":null,"start":41844743,"end":41852333,"strand":1,"description":"DMRT like family C2 [Source:HGNC Symbol;Acc:HGNC:13911]"}, {"versioned_ensembl_gene_id":"ENSG00000248349.1","gene_symbol":"AC112204.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35896188,"end":35896290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262519.1","gene_symbol":"TXNP4","gene_name":"thioredoxin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"124974","summary":null,"start":4572206,"end":4572515,"strand":1,"description":"thioredoxin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49484]"}, {"versioned_ensembl_gene_id":"ENSG00000211973.2","gene_symbol":"IGHV1-69","gene_name":"immunoglobulin heavy variable 1-69 [Source:HGNC Symbol;Acc:HGNC:5558]","synonyms":"IGHV1-E","biotype":"IG_V_gene","ncbi_id":"28461","summary":null,"start":106714684,"end":106715181,"strand":-1,"description":"immunoglobulin heavy variable 1-69 [Source:HGNC Symbol;Acc:HGNC:5558]"}, {"versioned_ensembl_gene_id":"ENSG00000270347.1","gene_symbol":"AC011453.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53657400,"end":53658462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164342.12","gene_symbol":"TLR3","gene_name":"toll like receptor 3 [Source:HGNC Symbol;Acc:HGNC:11849]","synonyms":"CD283","biotype":"protein_coding","ncbi_id":"7098","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This receptor is most abundantly expressed in placenta and pancreas, and is restricted to the dendritic subpopulation of the leukocytes. It recognizes dsRNA associated with viral infection, and induces the activation of NF-kappaB and the production of type I interferons. It may thus play a role in host defense against viruses. Use of alternative polyadenylation sites to generate different length transcripts has been noted for this gene. [provided by RefSeq, Jul 2008]","start":186069152,"end":186088069,"strand":1,"description":"toll like receptor 3 [Source:HGNC Symbol;Acc:HGNC:11849]"}, {"versioned_ensembl_gene_id":"ENSG00000143653.9","gene_symbol":"SCCPDH","gene_name":"saccharopine dehydrogenase (putative) [Source:HGNC Symbol;Acc:HGNC:24275]","synonyms":"NET11,CGI-49","biotype":"protein_coding","ncbi_id":"51097","summary":null,"start":246724047,"end":246768137,"strand":1,"description":"saccharopine dehydrogenase (putative) [Source:HGNC Symbol;Acc:HGNC:24275]"}, {"versioned_ensembl_gene_id":"ENSG00000276218.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2a,nkat2b,p58,CD158B2,cl-6,nkat2","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738484,"end":54752990,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000149639.14","gene_symbol":"SOGA1","gene_name":"suppressor of glucose, autophagy associated 1 [Source:HGNC Symbol;Acc:HGNC:16111]","synonyms":"SOGA,KIAA0889,FLJ44670,dJ132F21.1,C20orf117","biotype":"protein_coding","ncbi_id":"140710","summary":null,"start":36777442,"end":36863686,"strand":-1,"description":"suppressor of glucose, autophagy associated 1 [Source:HGNC Symbol;Acc:HGNC:16111]"}, {"versioned_ensembl_gene_id":"ENSG00000060656.19","gene_symbol":"PTPRU","gene_name":"protein tyrosine phosphatase, receptor type U [Source:HGNC Symbol;Acc:HGNC:9683]","synonyms":"PTPRO,PTP,PCP-2,hPTP-J,FMI","biotype":"protein_coding","ncbi_id":"10076","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP (MAM) domain, Ig-like and fibronectin type III-like repeats. This PTP was thought to play roles in cell-cell recognition and adhesion. Studies of the similar gene in mice suggested the role of this PTP in early neural development. The expression of this gene was reported to be regulated by phorbol myristate acetate (PMA) or calcium ionophore in Jurkat T lymphoma cells. Alternatively spliced transcript variants have been reported. [provided by RefSeq, Aug 2010]","start":29236516,"end":29326813,"strand":1,"description":"protein tyrosine phosphatase, receptor type U [Source:HGNC Symbol;Acc:HGNC:9683]"}, {"versioned_ensembl_gene_id":"ENSG00000267440.1","gene_symbol":"AC004149.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43680273,"end":43705884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261641.2","gene_symbol":"AL031600.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1445343,"end":1446519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171316.11","gene_symbol":"CHD7","gene_name":"chromodomain helicase DNA binding protein 7 [Source:HGNC Symbol;Acc:HGNC:20626]","synonyms":"FLJ20357,CRG,KIAA1416,FLJ20361","biotype":"protein_coding","ncbi_id":"55636","summary":"This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":60678778,"end":60868028,"strand":1,"description":"chromodomain helicase DNA binding protein 7 [Source:HGNC Symbol;Acc:HGNC:20626]"}, {"versioned_ensembl_gene_id":"ENSG00000251214.1","gene_symbol":"AC025465.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124459912,"end":124460549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223933.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"Em:AB014080.3,TMPOL1","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30456371,"end":30457898,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000232095.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30352921,"end":30354089,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000164211.12","gene_symbol":"STARD4","gene_name":"StAR related lipid transfer domain containing 4 [Source:HGNC Symbol;Acc:HGNC:18058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"134429","summary":"Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD4 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008]","start":111496033,"end":111512590,"strand":-1,"description":"StAR related lipid transfer domain containing 4 [Source:HGNC Symbol;Acc:HGNC:18058]"}, {"versioned_ensembl_gene_id":"ENSG00000228373.2","gene_symbol":"AL353752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87423634,"end":87423893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232277.1","gene_symbol":"AC104651.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111952144,"end":111952671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197841.14","gene_symbol":"ZNF181","gene_name":"zinc finger protein 181 [Source:HGNC Symbol;Acc:HGNC:12971]","synonyms":"MGC44316,HHZ181","biotype":"protein_coding","ncbi_id":"339318","summary":"Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2003]","start":34734155,"end":34745378,"strand":1,"description":"zinc finger protein 181 [Source:HGNC Symbol;Acc:HGNC:12971]"}, {"versioned_ensembl_gene_id":"ENSG00000180176.14","gene_symbol":"TH","gene_name":"tyrosine hydroxylase [Source:HGNC Symbol;Acc:HGNC:11782]","synonyms":"DYT5b","biotype":"protein_coding","ncbi_id":"7054","summary":"The protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]","start":2163929,"end":2171877,"strand":-1,"description":"tyrosine hydroxylase [Source:HGNC Symbol;Acc:HGNC:11782]"}, {"versioned_ensembl_gene_id":"ENSG00000279103.1","gene_symbol":"AC138470.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44246478,"end":44248374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261654.1","gene_symbol":"AL360270.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":110936369,"end":110942353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235555.1","gene_symbol":"SUMO1P4","gene_name":"SUMO1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101290502","summary":null,"start":49275119,"end":49275420,"strand":1,"description":"SUMO1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33151]"}, {"versioned_ensembl_gene_id":"ENSG00000172232.9","gene_symbol":"AZU1","gene_name":"azurocidin 1 [Source:HGNC Symbol;Acc:HGNC:913]","synonyms":"HBP,CAP37,AZU,AZAMP,NAZC,HUMAZUR","biotype":"protein_coding","ncbi_id":"566","summary":"Azurophil granules, specialized lysosomes of the neutrophil, contain at least 10 proteins implicated in the killing of microorganisms. This gene encodes a preproprotein that is proteolytically processed to generate a mature azurophil granule antibiotic protein, with monocyte chemotactic and antimicrobial activity. It is also an important multifunctional inflammatory mediator. This encoded protein is a member of the serine protease gene family but it is not a serine proteinase, because the active site serine and histidine residues are replaced. The genes encoding this protein, neutrophil elastase 2, and proteinase 3 are in a cluster located at chromosome 19pter. All 3 genes are expressed coordinately and their protein products are packaged together into azurophil granules during neutrophil differentiation. [provided by RefSeq, Nov 2015]","start":825097,"end":832018,"strand":1,"description":"azurocidin 1 [Source:HGNC Symbol;Acc:HGNC:913]"}, {"versioned_ensembl_gene_id":"ENSG00000225496.1","gene_symbol":"AC104651.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111940302,"end":111941036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138629.15","gene_symbol":"UBL7","gene_name":"ubiquitin like 7 [Source:HGNC Symbol;Acc:HGNC:28221]","synonyms":"MGC14421,BMSC-UbP","biotype":"protein_coding","ncbi_id":"84993","summary":null,"start":74445977,"end":74461182,"strand":-1,"description":"ubiquitin like 7 [Source:HGNC Symbol;Acc:HGNC:28221]"}, {"versioned_ensembl_gene_id":"ENSG00000131165.14","gene_symbol":"CHMP1A","gene_name":"charged multivesicular body protein 1A [Source:HGNC Symbol;Acc:HGNC:8740]","synonyms":"Vps46A,PRSM1,PCOLN3,KIAA0047,CHMP1","biotype":"protein_coding","ncbi_id":"5119","summary":"This gene encodes a member of the CHMP/Chmp family of proteins which are involved in multivesicular body sorting of proteins to the interiors of lysosomes. The initial prediction of the protein sequence encoded by this gene suggested that the encoded protein was a metallopeptidase. The nomenclature has been updated recently to reflect the correct biological function of this encoded protein. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":89644431,"end":89657845,"strand":-1,"description":"charged multivesicular body protein 1A [Source:HGNC Symbol;Acc:HGNC:8740]"}, {"versioned_ensembl_gene_id":"ENSG00000172819.16","gene_symbol":"RARG","gene_name":"retinoic acid receptor gamma [Source:HGNC Symbol;Acc:HGNC:9866]","synonyms":"RARC,NR1B3","biotype":"protein_coding","ncbi_id":"5916","summary":"This gene encodes a retinoic acid receptor that belongs to the nuclear hormone receptor family. Retinoic acid receptors (RARs) act as ligand-dependent transcriptional regulators. When bound to ligands, RARs activate transcription by binding as heterodimers to the retinoic acid response elements (RARE) found in the promoter regions of the target genes. In their unbound form, RARs repress transcription of their target genes. RARs are involved in various biological processes, including limb bud development, skeletal growth, and matrix homeostasis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":53210567,"end":53232980,"strand":-1,"description":"retinoic acid receptor gamma [Source:HGNC Symbol;Acc:HGNC:9866]"}, {"versioned_ensembl_gene_id":"ENSG00000278001.1","gene_symbol":"AL591926.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41700682,"end":41701096,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274688.1","gene_symbol":"AL591926.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41700480,"end":41700696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277979.1","gene_symbol":"AL591926.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41652895,"end":41652973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276135.1","gene_symbol":"FAM27E2","gene_name":"family with sequence similarity 27 member E2 [Source:HGNC Symbol;Acc:HGNC:32013]","synonyms":"FAM27E1","biotype":"processed_pseudogene","ncbi_id":"100289124","summary":null,"start":41648023,"end":41648425,"strand":1,"description":"family with sequence similarity 27 member E2 [Source:HGNC Symbol;Acc:HGNC:32013]"}, {"versioned_ensembl_gene_id":"ENSG00000253747.1","gene_symbol":"IGHVII-62-1","gene_name":"immunoglobulin heavy variable (II)-62-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5687]","synonyms":"IGHV(II)-62-1","biotype":"IG_V_pseudogene","ncbi_id":"28360","summary":null,"start":106650551,"end":106650785,"strand":-1,"description":"immunoglobulin heavy variable (II)-62-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5687]"}, {"versioned_ensembl_gene_id":"ENSG00000234200.2","gene_symbol":"AC243591.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153028785,"end":153030148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211970.3","gene_symbol":"IGHV4-61","gene_name":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28391","summary":null,"start":106639119,"end":106639657,"strand":-1,"description":"immunoglobulin heavy variable 4-61 [Source:HGNC Symbol;Acc:HGNC:5655]"}, {"versioned_ensembl_gene_id":"ENSG00000205636.3","gene_symbol":"LINC00583","gene_name":"long intergenic non-protein coding RNA 583 [Source:HGNC Symbol;Acc:HGNC:31437]","synonyms":"C9orf146","biotype":"lincRNA","ncbi_id":"100113404","summary":null,"start":13927971,"end":13945610,"strand":1,"description":"long intergenic non-protein coding RNA 583 [Source:HGNC Symbol;Acc:HGNC:31437]"}, {"versioned_ensembl_gene_id":"ENSG00000229268.1","gene_symbol":"PES1P2","gene_name":"pescadillo ribosomal biogenesis factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44059]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347193","summary":null,"start":13986175,"end":13987909,"strand":1,"description":"pescadillo ribosomal biogenesis factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44059]"}, {"versioned_ensembl_gene_id":"ENSG00000235858.1","gene_symbol":"AL359195.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80333771,"end":80334426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198113.2","gene_symbol":"TOR4A","gene_name":"torsin family 4 member A [Source:HGNC Symbol;Acc:HGNC:25981]","synonyms":"FLJ20245,C9orf167","biotype":"protein_coding","ncbi_id":"54863","summary":null,"start":137277749,"end":137282641,"strand":1,"description":"torsin family 4 member A [Source:HGNC Symbol;Acc:HGNC:25981]"}, {"versioned_ensembl_gene_id":"ENSG00000128050.8","gene_symbol":"PAICS","gene_name":"phosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase [Source:HGNC Symbol;Acc:HGNC:8587]","synonyms":"PAIS,AIRC,ADE2H1","biotype":"protein_coding","ncbi_id":"10606","summary":"This gene encodes a bifunctional enzyme containing phosphoribosylaminoimidazole carboxylase activity in its N-terminal region and phosphoribosylaminoimidazole succinocarboxamide synthetase in its C-terminal region. It catalyzes steps 6 and 7 of purine biosynthesis. The gene is closely linked and divergently transcribed with a locus that encodes an enzyme in the same pathway, and transcription of the two genes is coordinately regulated. The human genome contains several pseudogenes of this gene. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56435741,"end":56464579,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase [Source:HGNC Symbol;Acc:HGNC:8587]"}, {"versioned_ensembl_gene_id":"ENSG00000067596.10","gene_symbol":"DHX8","gene_name":"DEAH-box helicase 8 [Source:HGNC Symbol;Acc:HGNC:2749]","synonyms":"PRPF22,PRP22,HRH1,Dhr2,DDX8","biotype":"protein_coding","ncbi_id":"1659","summary":"This gene is a member of the DEAH box polypeptide family. The encoded protein contains the DEAH (Asp-Glu-Ala-His) motif which is characteristic of all DEAH box proteins, and is thought to function as an ATP-dependent RNA helicase that regulates the release of spliced mRNAs from spliceosomes prior to their export from the nucleus. This protein may be required for the replication of human immunodeficiency virus type 1 (HIV-1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":43483865,"end":43544463,"strand":1,"description":"DEAH-box helicase 8 [Source:HGNC Symbol;Acc:HGNC:2749]"}, {"versioned_ensembl_gene_id":"ENSG00000232950.1","gene_symbol":"ZNF519P1","gene_name":"zinc finger protein 519 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419873","summary":null,"start":80297720,"end":80299655,"strand":1,"description":"zinc finger protein 519 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50785]"}, {"versioned_ensembl_gene_id":"ENSG00000248590.2","gene_symbol":"GLDCP1","gene_name":"glycine decarboxylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4314]","synonyms":"GLDCP","biotype":"transcribed_processed_pseudogene","ncbi_id":"2732","summary":null,"start":56593004,"end":56595681,"strand":1,"description":"glycine decarboxylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4314]"}, {"versioned_ensembl_gene_id":"ENSG00000180447.6","gene_symbol":"GAS1","gene_name":"growth arrest specific 1 [Source:HGNC Symbol;Acc:HGNC:4165]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2619","summary":"Growth arrest-specific 1 plays a role in growth suppression. GAS1 blocks entry to S phase and prevents cycling of normal and transformed cells. Gas1 is a putative tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":86944363,"end":86947189,"strand":-1,"description":"growth arrest specific 1 [Source:HGNC Symbol;Acc:HGNC:4165]"}, {"versioned_ensembl_gene_id":"ENSG00000235819.1","gene_symbol":"AL158828.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86414282,"end":86414570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214908.3","gene_symbol":"AL353678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86374966,"end":86375706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238181.2","gene_symbol":"AHCYP2","gene_name":"adenosylhomocysteinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392387","summary":null,"start":120720673,"end":120721972,"strand":1,"description":"adenosylhomocysteinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44994]"}, {"versioned_ensembl_gene_id":"ENSG00000273611.4","gene_symbol":"ZNHIT3","gene_name":"zinc finger HIT-type containing 3 [Source:HGNC Symbol;Acc:HGNC:12309]","synonyms":"TRIP3","biotype":"protein_coding","ncbi_id":"9326","summary":null,"start":36486629,"end":36499310,"strand":1,"description":"zinc finger HIT-type containing 3 [Source:HGNC Symbol;Acc:HGNC:12309]"}, {"versioned_ensembl_gene_id":"ENSG00000242267.6","gene_symbol":"SKINT1L","gene_name":"Skint1 like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33993]","synonyms":"SKINTL,BTN12,SKINTP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"391037","summary":null,"start":48096092,"end":48182428,"strand":-1,"description":"Skint1 like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33993]"}, {"versioned_ensembl_gene_id":"ENSG00000223720.2","gene_symbol":"AL109659.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48172972,"end":48206857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232216.1","gene_symbol":"IGHV3-43","gene_name":"immunoglobulin heavy variable 3-43 [Source:HGNC Symbol;Acc:HGNC:5604]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28426","summary":null,"start":106470264,"end":106470800,"strand":-1,"description":"immunoglobulin heavy variable 3-43 [Source:HGNC Symbol;Acc:HGNC:5604]"}, {"versioned_ensembl_gene_id":"ENSG00000283195.1","gene_symbol":"AC244452.3","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106472791,"end":106473000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100461.17","gene_symbol":"RBM23","gene_name":"RNA binding motif protein 23 [Source:HGNC Symbol;Acc:HGNC:20155]","synonyms":"RNPC4,FLJ10482,CAPERbeta","biotype":"protein_coding","ncbi_id":"55147","summary":"This gene encodes a member of the U2AF-like family of RNA binding proteins. This protein interacts with some steroid nuclear receptors, localizes to the promoter of a steroid- responsive gene, and increases transcription of steroid-responsive transcriptional reporters in a hormone-dependent manner. It is also implicated in the steroid receptor-dependent regulation of alternative splicing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":22893206,"end":22919184,"strand":-1,"description":"RNA binding motif protein 23 [Source:HGNC Symbol;Acc:HGNC:20155]"}, {"versioned_ensembl_gene_id":"ENSG00000276248.1","gene_symbol":"AL442125.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113527260,"end":113530621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257585.1","gene_symbol":"LINC00609","gene_name":"long intergenic non-protein coding RNA 609 [Source:HGNC Symbol;Acc:HGNC:43960]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101101773","summary":null,"start":36070427,"end":36165288,"strand":1,"description":"long intergenic non-protein coding RNA 609 [Source:HGNC Symbol;Acc:HGNC:43960]"}, {"versioned_ensembl_gene_id":"ENSG00000255193.1","gene_symbol":"AC100768.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23730588,"end":23796970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254861.1","gene_symbol":"AC100768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23761330,"end":23804598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234004.4","gene_symbol":"AC092017.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":211173488,"end":211173849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186919.12","gene_symbol":"ZACN","gene_name":"zinc activated ion channel [Source:HGNC Symbol;Acc:HGNC:29504]","synonyms":"LGICZ1,LGICZ,L2,ZAC1,ZAC","biotype":"protein_coding","ncbi_id":"353174","summary":"LGICZ1 is a zinc-activated ligand-gated ion channel that defines a new subgroup of the cysteine-loop superfamily of ligand-gated ion channels (Davies et al., 2003 [PubMed 12381728]).[supplied by OMIM, Mar 2008]","start":76071961,"end":76083666,"strand":1,"description":"zinc activated ion channel [Source:HGNC Symbol;Acc:HGNC:29504]"}, {"versioned_ensembl_gene_id":"ENSG00000181273.2","gene_symbol":"OR5AK2","gene_name":"olfactory receptor family 5 subfamily AK member 2 [Source:HGNC Symbol;Acc:HGNC:15251]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390181","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56988872,"end":56989867,"strand":1,"description":"olfactory receptor family 5 subfamily AK member 2 [Source:HGNC Symbol;Acc:HGNC:15251]"}, {"versioned_ensembl_gene_id":"ENSG00000130844.16","gene_symbol":"ZNF331","gene_name":"zinc finger protein 331 [Source:HGNC Symbol;Acc:HGNC:15489]","synonyms":"ZNF463,ZNF361,RITA","biotype":"protein_coding","ncbi_id":"55422","summary":"This gene encodes a zinc finger protein containing a KRAB (Kruppel-associated box) domain found in transcriptional repressors. This gene may be methylated and silenced in cancer cells. This gene is located within a differentially methylated region (DMR) and shows allele-specific expression in placenta. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding the same protein. [provided by RefSeq, Nov 2015]","start":53520981,"end":53580269,"strand":1,"description":"zinc finger protein 331 [Source:HGNC Symbol;Acc:HGNC:15489]"}, {"versioned_ensembl_gene_id":"ENSG00000251471.1","gene_symbol":"AC016933.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139837220,"end":139859894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224894.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"PsiGPR53,dJ271M21.8","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537652,"end":29538442,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000177272.8","gene_symbol":"KCNA3","gene_name":"potassium voltage-gated channel subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:6221]","synonyms":"HLK3,MK3,Kv1.3,HPCN3","biotype":"protein_coding","ncbi_id":"3738","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, members of which allow nerve cells to efficiently repolarize following an action potential. It plays an essential role in T-cell proliferation and activation. This gene appears to be intronless and it is clustered together with KCNA2 and KCNA10 genes on chromosome 1. [provided by RefSeq, Jul 2008]","start":110672465,"end":110675033,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:6221]"}, {"versioned_ensembl_gene_id":"ENSG00000256745.1","gene_symbol":"AP002784.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94188449,"end":94188997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250535.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"bPG116M5.10,STK19P,RP2","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":32013270,"end":32013787,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000163421.8","gene_symbol":"PROK2","gene_name":"prokineticin 2 [Source:HGNC Symbol;Acc:HGNC:18455]","synonyms":"PK2,MIT1,KAL4,BV8","biotype":"protein_coding","ncbi_id":"60675","summary":"This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":71771656,"end":71785206,"strand":-1,"description":"prokineticin 2 [Source:HGNC Symbol;Acc:HGNC:18455]"}, {"versioned_ensembl_gene_id":"ENSG00000284667.1","gene_symbol":"AC064853.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227666804,"end":227667061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223891.5","gene_symbol":"OSER1-AS1","gene_name":"OSER1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48585]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505783","summary":null,"start":44210960,"end":44226027,"strand":1,"description":"OSER1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48585]"}, {"versioned_ensembl_gene_id":"ENSG00000253367.1","gene_symbol":"IGHVIII-25-1","gene_name":"immunoglobulin heavy variable (III)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5697]","synonyms":"IGHV(III)-25-1","biotype":"IG_V_pseudogene","ncbi_id":"28348","summary":null,"start":106293568,"end":106293808,"strand":-1,"description":"immunoglobulin heavy variable (III)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5697]"}, {"versioned_ensembl_gene_id":"ENSG00000253441.1","gene_symbol":"IGHV3-25","gene_name":"immunoglobulin heavy variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5589]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28441","summary":null,"start":106289029,"end":106289479,"strand":-1,"description":"immunoglobulin heavy variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5589]"}, {"versioned_ensembl_gene_id":"ENSG00000250728.1","gene_symbol":"AC010468.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111155244,"end":111156152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163814.7","gene_symbol":"CDCP1","gene_name":"CUB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:24357]","synonyms":"SIMA135,CD318","biotype":"protein_coding","ncbi_id":"64866","summary":"This gene encodes a transmembrane protein which contains three extracellular CUB domains and acts as a substrate for Src family kinases. The protein plays a role in the tyrosine phosphorylation-dependent regulation of cellular events that are involved in tumor invasion and metastasis. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":45082278,"end":45146422,"strand":-1,"description":"CUB domain containing protein 1 [Source:HGNC Symbol;Acc:HGNC:24357]"}, {"versioned_ensembl_gene_id":"ENSG00000276755.1","gene_symbol":"AC243829.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36234447,"end":36234554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261821.2","gene_symbol":"AC090826.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74365435,"end":74371211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229463.2","gene_symbol":"LYST-AS1","gene_name":"LYST antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41320]","synonyms":"LYST-IT2","biotype":"antisense_RNA","ncbi_id":"100874266","summary":null,"start":235839483,"end":235840182,"strand":1,"description":"LYST antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41320]"}, {"versioned_ensembl_gene_id":"ENSG00000254076.1","gene_symbol":"AC110053.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137696724,"end":137698467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225276.1","gene_symbol":"MTND1P18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42067]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873338","summary":null,"start":37600796,"end":37601368,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42067]"}, {"versioned_ensembl_gene_id":"ENSG00000264304.1","gene_symbol":"AC024267.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28892469,"end":28893342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186019.10","gene_symbol":"AC021092.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44105463,"end":44113145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223652.2","gene_symbol":"AC106786.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123087248,"end":123090299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258342.1","gene_symbol":"AL133304.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":35897982,"end":36063743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262560.1","gene_symbol":"AC018512.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43772617,"end":43799133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225083.1","gene_symbol":"GRTP1-AS1","gene_name":"GRTP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39917]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874068","summary":null,"start":113351673,"end":113361868,"strand":1,"description":"GRTP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39917]"}, {"versioned_ensembl_gene_id":"ENSG00000232192.1","gene_symbol":"AL592103.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":245206444,"end":245234501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234309.1","gene_symbol":"SLC25A18P1","gene_name":"solute carrier family 25 member 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43857]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480776","summary":null,"start":118572871,"end":118573620,"strand":1,"description":"solute carrier family 25 member 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43857]"}, {"versioned_ensembl_gene_id":"ENSG00000213293.4","gene_symbol":"AC012618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12260126,"end":12260537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243297.2","gene_symbol":"RPL31P61","gene_name":"ribosomal protein L31 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:35635]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271487","summary":null,"start":36901742,"end":36902117,"strand":1,"description":"ribosomal protein L31 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:35635]"}, {"versioned_ensembl_gene_id":"ENSG00000177261.8","gene_symbol":"ENSAP3","gene_name":"endosulfine alpha pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128203","summary":null,"start":214697727,"end":214698059,"strand":1,"description":"endosulfine alpha pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37946]"}, {"versioned_ensembl_gene_id":"ENSG00000168517.10","gene_symbol":"HEXIM2","gene_name":"hexamethylene bisacetamide inducible 2 [Source:HGNC Symbol;Acc:HGNC:28591]","synonyms":"FLJ32384","biotype":"protein_coding","ncbi_id":"124790","summary":"This gene encodes a member of the HEXIM family of proteins. This protein is a component of the 7SK small nuclear ribonucleoprotein. This protein has been found to negatively regulate the kinase activity of the cyclin-dependent kinase P-TEFb, which phosphorylates multiple target proteins to promote transcriptional elongation. This gene is located approximately 7 kb downstream from related family member HEXIM1 on chromosome 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":45160700,"end":45170040,"strand":1,"description":"hexamethylene bisacetamide inducible 2 [Source:HGNC Symbol;Acc:HGNC:28591]"}, {"versioned_ensembl_gene_id":"ENSG00000273894.1","gene_symbol":"SLC20A1P2","gene_name":"solute carrier family 20 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192128","summary":null,"start":106179554,"end":106180519,"strand":-1,"description":"solute carrier family 20 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42539]"}, {"versioned_ensembl_gene_id":"ENSG00000188026.12","gene_symbol":"RILPL1","gene_name":"Rab interacting lysosomal protein like 1 [Source:HGNC Symbol;Acc:HGNC:26814]","synonyms":"FLJ39378","biotype":"protein_coding","ncbi_id":"353116","summary":null,"start":123470054,"end":123533718,"strand":-1,"description":"Rab interacting lysosomal protein like 1 [Source:HGNC Symbol;Acc:HGNC:26814]"}, {"versioned_ensembl_gene_id":"ENSG00000167526.13","gene_symbol":"RPL13","gene_name":"ribosomal protein L13 [Source:HGNC Symbol;Acc:HGNC:10303]","synonyms":"L13,D16S444E,BBC1","biotype":"protein_coding","ncbi_id":"6137","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L13E family of ribosomal proteins. It is located in the cytoplasm. This gene is expressed at significantly higher levels in benign breast lesions than in breast carcinomas. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2011]","start":89560657,"end":89566828,"strand":1,"description":"ribosomal protein L13 [Source:HGNC Symbol;Acc:HGNC:10303]"}, {"versioned_ensembl_gene_id":"ENSG00000132478.9","gene_symbol":"UNK","gene_name":"unkempt family zinc finger [Source:HGNC Symbol;Acc:HGNC:29369]","synonyms":"ZC3HDC5,ZC3H5,KIAA1753","biotype":"protein_coding","ncbi_id":"85451","summary":null,"start":75784771,"end":75825799,"strand":1,"description":"unkempt family zinc finger [Source:HGNC Symbol;Acc:HGNC:29369]"}, {"versioned_ensembl_gene_id":"ENSG00000086570.12","gene_symbol":"FAT2","gene_name":"FAT atypical cadherin 2 [Source:HGNC Symbol;Acc:HGNC:3596]","synonyms":"MEGF1,HFAT2,CDHR9,CDHF8","biotype":"protein_coding","ncbi_id":"2196","summary":"This gene is the second identified human homolog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has two epidermal growth factor (EGF)-like repeats and one laminin G domain. This protein most likely functions as a cell adhesion molecule, controlling cell proliferation and playing an important role in cerebellum development. [provided by RefSeq, Jul 2008]","start":151504093,"end":151568944,"strand":-1,"description":"FAT atypical cadherin 2 [Source:HGNC Symbol;Acc:HGNC:3596]"}, {"versioned_ensembl_gene_id":"ENSG00000258125.1","gene_symbol":"AC025254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91680131,"end":91680873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254174.1","gene_symbol":"IGHV1-12","gene_name":"immunoglobulin heavy variable 1-12 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5546]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28471","summary":null,"start":106122420,"end":106122709,"strand":-1,"description":"immunoglobulin heavy variable 1-12 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5546]"}, {"versioned_ensembl_gene_id":"ENSG00000186432.8","gene_symbol":"KPNA4","gene_name":"karyopherin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6397]","synonyms":"SRP3,QIP1,MGC26703,MGC12217,IPOA3","biotype":"protein_coding","ncbi_id":"3840","summary":"The nuclear import of karyophilic proteins is directed by short amino acid sequences termed nuclear localization signals (NLSs). Karyopherins, or importins, are cytoplasmic proteins that recognize NLSs and dock NLS-containing proteins to the nuclear pore complex. The protein encoded by this gene shares the sequence similarity with Xenopus importin-alpha and Saccharomyces cerevisiae Srp1. This protein is found to interact with the NLSs of DNA helicase Q1 and SV40 T antigen. [provided by RefSeq, Jul 2008]","start":160494995,"end":160565588,"strand":-1,"description":"karyopherin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6397]"}, {"versioned_ensembl_gene_id":"ENSG00000277078.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54863003,"end":54878657,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000258448.1","gene_symbol":"AL442663.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73068108,"end":73068618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227282.1","gene_symbol":"AL389889.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59515191,"end":59516039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253897.1","gene_symbol":"AC034205.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151366433,"end":151431352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275302.1","gene_symbol":"CCL4","gene_name":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]","synonyms":"SCYA4,MIP-1-beta,MIP-1-beta,LAG1,LAG1,AT744.1,AT744.1,Act-2,Act-2,SCYA4","biotype":"protein_coding","ncbi_id":"6351","summary":"The protein encoded by this gene is a mitogen-inducible monokine and is one of the major HIV-suppressive factors produced by CD8+ T-cells. The encoded protein is secreted and has chemokinetic and inflammatory functions. [provided by RefSeq, Dec 2012]","start":36103590,"end":36105621,"strand":1,"description":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]"}, {"versioned_ensembl_gene_id":"ENSG00000281398.2","gene_symbol":"SNHG4","gene_name":"small nucleolar RNA host gene 4 [Source:HGNC Symbol;Acc:HGNC:32964]","synonyms":"U19H,NCRNA00059","biotype":"processed_transcript","ncbi_id":"724102","summary":null,"start":139274102,"end":139283244,"strand":1,"description":"small nucleolar RNA host gene 4 [Source:HGNC Symbol;Acc:HGNC:32964]"}, {"versioned_ensembl_gene_id":"ENSG00000059691.11","gene_symbol":"GATB","gene_name":"glutamyl-tRNA amidotransferase subunit B [Source:HGNC Symbol;Acc:HGNC:8849]","synonyms":"PET112L,PET112","biotype":"protein_coding","ncbi_id":"5188","summary":null,"start":151670504,"end":151761023,"strand":-1,"description":"glutamyl-tRNA amidotransferase subunit B [Source:HGNC Symbol;Acc:HGNC:8849]"}, {"versioned_ensembl_gene_id":"ENSG00000277566.1","gene_symbol":"AC089999.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113249466,"end":113250042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228694.1","gene_symbol":"MTND4P18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42205]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873350","summary":null,"start":36434710,"end":36435174,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42205]"}, {"versioned_ensembl_gene_id":"ENSG00000280878.1","gene_symbol":"AC017002.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111468810,"end":111637967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225744.1","gene_symbol":"AC017002.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111607841,"end":111612518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110090.12","gene_symbol":"CPT1A","gene_name":"carnitine palmitoyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:2328]","synonyms":"L-CPT1,CPT1-L,CPT1","biotype":"protein_coding","ncbi_id":"1374","summary":"The mitochondrial oxidation of long-chain fatty acids is initiated by the sequential action of carnitine palmitoyltransferase I (which is located in the outer membrane and is detergent-labile) and carnitine palmitoyltransferase II (which is located in the inner membrane and is detergent-stable), together with a carnitine-acylcarnitine translocase. CPT I is the key enzyme in the carnitine-dependent transport across the mitochondrial inner membrane and its deficiency results in a decreased rate of fatty acid beta-oxidation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68754620,"end":68844410,"strand":-1,"description":"carnitine palmitoyltransferase 1A [Source:HGNC Symbol;Acc:HGNC:2328]"}, {"versioned_ensembl_gene_id":"ENSG00000259162.1","gene_symbol":"AL355075.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20437982,"end":20441268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237842.2","gene_symbol":"AL157713.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157059232,"end":157060762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104818.14","gene_symbol":"CGB2","gene_name":"chorionic gonadotropin beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:16722]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114336","summary":"The beta subunit of chorionic gonadotropin (CGB) is encoded by six highly homologous and structurally similar genes that are arranged in tandem and inverted pairs on chromosome 19q13.3, and contiguous with the luteinizing hormone beta (LHB) subunit gene. The CGB genes are primarily distinguished by differences in the 5' untranscribed region. This gene was originally thought to be one of the two pseudogenes (CGB1 and CGB2) of CGB subunit, however, detection of CGB1 and CGB2 transcripts in vivo, and their presence on the polysomes, suggested that these transcripts are translated. To date, a protein product corresponding to CGB2 has not been isolated. The deduced sequence of the hypothetical protein of 132 aa does not share any similarity with that of functional CGB subunits (PMID:8954017). However, a 163 aa protein, translated from a different frame, is about the same size, and shares 98% identity with other CGB subunits. [provided by RefSeq, Jul 2008]","start":49031912,"end":49033238,"strand":1,"description":"chorionic gonadotropin beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:16722]"}, {"versioned_ensembl_gene_id":"ENSG00000267755.1","gene_symbol":"AC005329.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1376773,"end":1377520,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177839.6","gene_symbol":"PCDHB9","gene_name":"protocadherin beta 9 [Source:HGNC Symbol;Acc:HGNC:8694]","synonyms":"PCDH-BETA9,PCDH3H","biotype":"protein_coding","ncbi_id":"56127","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141187127,"end":141191541,"strand":1,"description":"protocadherin beta 9 [Source:HGNC Symbol;Acc:HGNC:8694]"}, {"versioned_ensembl_gene_id":"ENSG00000228007.1","gene_symbol":"AC011933.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75338827,"end":75339147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268902.3","gene_symbol":"CSAG2","gene_name":"CSAG family member 2 [Source:HGNC Symbol;Acc:HGNC:16847]","synonyms":"TRAG3,CT24.2,CSAG3B","biotype":"protein_coding","ncbi_id":"102723547","summary":null,"start":152708261,"end":152714549,"strand":-1,"description":"CSAG family member 2 [Source:HGNC Symbol;Acc:HGNC:16847]"}, {"versioned_ensembl_gene_id":"ENSG00000113205.5","gene_symbol":"PCDHB3","gene_name":"protocadherin beta 3 [Source:HGNC Symbol;Acc:HGNC:8688]","synonyms":"PCDH-BETA3","biotype":"protein_coding","ncbi_id":"56132","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141100473,"end":141103827,"strand":1,"description":"protocadherin beta 3 [Source:HGNC Symbol;Acc:HGNC:8688]"}, {"versioned_ensembl_gene_id":"ENSG00000225960.1","gene_symbol":"AL441989.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119973094,"end":119974322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263843.1","gene_symbol":"AC022211.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75271369,"end":75273895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267058.1","gene_symbol":"AC006213.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43891804,"end":43901805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162367.11","gene_symbol":"TAL1","gene_name":"TAL bHLH transcription factor 1, erythroid differentiation factor [Source:HGNC Symbol;Acc:HGNC:11556]","synonyms":"TCL5,SCL,bHLHa17","biotype":"protein_coding","ncbi_id":"6886","summary":null,"start":47216290,"end":47232220,"strand":-1,"description":"TAL bHLH transcription factor 1, erythroid differentiation factor [Source:HGNC Symbol;Acc:HGNC:11556]"}, {"versioned_ensembl_gene_id":"ENSG00000269637.1","gene_symbol":"RPL12P41","gene_name":"ribosomal protein L12 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35999]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133139","summary":null,"start":46219423,"end":46219920,"strand":1,"description":"ribosomal protein L12 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35999]"}, {"versioned_ensembl_gene_id":"ENSG00000275433.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54726054,"end":54736537,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000283208.1","gene_symbol":"AC001226.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76992078,"end":77129589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232355.2","gene_symbol":"AL603650.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":134868236,"end":134868475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099769.5","gene_symbol":"IGFALS","gene_name":"insulin like growth factor binding protein acid labile subunit [Source:HGNC Symbol;Acc:HGNC:5468]","synonyms":"ALS","biotype":"protein_coding","ncbi_id":"3483","summary":"The protein encoded by this gene is a serum protein that binds insulin-like growth factors, increasing their half-life and their vascular localization. Production of the encoded protein, which contains twenty leucine-rich repeats, is stimulated by growth hormone. Defects in this gene are a cause of acid-labile subunit deficiency, which maifests itself in a delayed and slow puberty. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":1790413,"end":1794971,"strand":-1,"description":"insulin like growth factor binding protein acid labile subunit [Source:HGNC Symbol;Acc:HGNC:5468]"}, {"versioned_ensembl_gene_id":"ENSG00000217495.2","gene_symbol":"AL136116.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143298770,"end":143299554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123444.13","gene_symbol":"KBTBD4","gene_name":"kelch repeat and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23761]","synonyms":"HSPC252,FLJ10450,BKLHD4","biotype":"protein_coding","ncbi_id":"55709","summary":null,"start":47572197,"end":47579015,"strand":-1,"description":"kelch repeat and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23761]"}, {"versioned_ensembl_gene_id":"ENSG00000225936.1","gene_symbol":"AL731557.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117239600,"end":117241923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164209.16","gene_symbol":"SLC25A46","gene_name":"solute carrier family 25 member 46 [Source:HGNC Symbol;Acc:HGNC:25198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91137","summary":"This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]","start":110738136,"end":110765161,"strand":1,"description":"solute carrier family 25 member 46 [Source:HGNC Symbol;Acc:HGNC:25198]"}, {"versioned_ensembl_gene_id":"ENSG00000251184.1","gene_symbol":"AL672142.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":128941478,"end":128957021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165646.11","gene_symbol":"SLC18A2","gene_name":"solute carrier family 18 member A2 [Source:HGNC Symbol;Acc:HGNC:10935]","synonyms":"VMAT2,SVMT,SVAT","biotype":"protein_coding","ncbi_id":"6571","summary":"This gene encodes an transmembrane protein that functions as an ATP-dependent transporter of monoamines, such as dopamine, norepinephrine, serotonin, and histamine. This protein transports amine neurotransmitters into synaptic vesicles. Polymorphisms in this gene may be associated with schizophrenia, bipolar disorder, and other neurological/psychiatric ailments. [provided by RefSeq, Jun 2018]","start":117241093,"end":117279430,"strand":1,"description":"solute carrier family 18 member A2 [Source:HGNC Symbol;Acc:HGNC:10935]"}, {"versioned_ensembl_gene_id":"ENSG00000248932.5","gene_symbol":"AC097103.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139389815,"end":139583319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237632.3","gene_symbol":"S100A11P1","gene_name":"S100 calcium binding protein A11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10491]","synonyms":"S100A14,S100A11P","biotype":"processed_pseudogene","ncbi_id":"729659","summary":null,"start":103262000,"end":103262311,"strand":1,"description":"S100 calcium binding protein A11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10491]"}, {"versioned_ensembl_gene_id":"ENSG00000227104.3","gene_symbol":"PIGQP1","gene_name":"phosphatidylinositol glycan anchor biosynthesis class Q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45157]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106480812","summary":null,"start":55938714,"end":55939280,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class Q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45157]"}, {"versioned_ensembl_gene_id":"ENSG00000214280.3","gene_symbol":"AC046134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139582928,"end":139583593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227247.1","gene_symbol":"TRIM60P13","gene_name":"tripartite motif containing 60 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38485]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132195","summary":null,"start":89248818,"end":89250100,"strand":-1,"description":"tripartite motif containing 60 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38485]"}, {"versioned_ensembl_gene_id":"ENSG00000232225.6","gene_symbol":"LINC01047","gene_name":"long intergenic non-protein coding RNA 1047 [Source:HGNC Symbol;Acc:HGNC:49041]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105616982","summary":null,"start":89214847,"end":89236890,"strand":-1,"description":"long intergenic non-protein coding RNA 1047 [Source:HGNC Symbol;Acc:HGNC:49041]"}, {"versioned_ensembl_gene_id":"ENSG00000213399.3","gene_symbol":"AC022210.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84915868,"end":84916660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136108.14","gene_symbol":"CKAP2","gene_name":"cytoskeleton associated protein 2 [Source:HGNC Symbol;Acc:HGNC:1990]","synonyms":"TMAP,se20-10,LB1,FLJ10749","biotype":"protein_coding","ncbi_id":"26586","summary":"This gene encodes a cytoskeleton-associated protein that stabalizes microtubules and plays a role in the regulation of cell division. The encoded protein is itself regulated through phosphorylation at multiple serine and threonine residues. There is a pseudogene of this gene on chromosome 14. Alternative splicing results in multiple transcript variations. [provided by RefSeq, Nov 2013]","start":52455429,"end":52476628,"strand":1,"description":"cytoskeleton associated protein 2 [Source:HGNC Symbol;Acc:HGNC:1990]"}, {"versioned_ensembl_gene_id":"ENSG00000237525.6","gene_symbol":"AC012668.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215533133,"end":215713895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234938.2","gene_symbol":"AC012668.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215530447,"end":215545526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270445.1","gene_symbol":"AC145423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123441517,"end":123441852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228300.13","gene_symbol":"C19orf24","gene_name":"chromosome 19 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:26073]","synonyms":"FLJ20640","biotype":"protein_coding","ncbi_id":"55009","summary":null,"start":1275438,"end":1279249,"strand":1,"description":"chromosome 19 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:26073]"}, {"versioned_ensembl_gene_id":"ENSG00000099330.8","gene_symbol":"OCEL1","gene_name":"occludin/ELL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26221]","synonyms":"FLJ22709","biotype":"protein_coding","ncbi_id":"79629","summary":null,"start":17226204,"end":17229219,"strand":1,"description":"occludin/ELL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26221]"}, {"versioned_ensembl_gene_id":"ENSG00000172071.11","gene_symbol":"EIF2AK3","gene_name":"eukaryotic translation initiation factor 2 alpha kinase 3 [Source:HGNC Symbol;Acc:HGNC:3255]","synonyms":"PERK,PEK","biotype":"protein_coding","ncbi_id":"9451","summary":"The protein encoded by this gene phosphorylates the alpha subunit of eukaryotic translation-initiation factor 2, leading to its inactivation, and thus to a rapid reduction of translational initiation and repression of global protein synthesis. This protein is thought to modulate mitochondrial function. It is a type I membrane protein located in the endoplasmic reticulum (ER), where it is induced by ER stress caused by malfolded proteins. Mutations in this gene are associated with Wolcott-Rallison syndrome. [provided by RefSeq, Sep 2015]","start":88556741,"end":88627576,"strand":-1,"description":"eukaryotic translation initiation factor 2 alpha kinase 3 [Source:HGNC Symbol;Acc:HGNC:3255]"}, {"versioned_ensembl_gene_id":"ENSG00000230230.7","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"RNF95,ZNF173","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30174354,"end":30203317,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000227048.2","gene_symbol":"AC096677.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":201428975,"end":201429361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236897.1","gene_symbol":"AC113331.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5106062,"end":5107530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166130.14","gene_symbol":"IKBIP","gene_name":"IKBKB interacting protein [Source:HGNC Symbol;Acc:HGNC:26430]","synonyms":"IKIP,FLJ31051","biotype":"protein_coding","ncbi_id":"121457","summary":null,"start":98613405,"end":98645113,"strand":-1,"description":"IKBKB interacting protein [Source:HGNC Symbol;Acc:HGNC:26430]"}, {"versioned_ensembl_gene_id":"ENSG00000282876.1","gene_symbol":"Z98752.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43590009,"end":43590596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224291.1","gene_symbol":"AC012671.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88428078,"end":88428615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164949.7","gene_symbol":"GEM","gene_name":"GTP binding protein overexpressed in skeletal muscle [Source:HGNC Symbol;Acc:HGNC:4234]","synonyms":"KIR","biotype":"protein_coding","ncbi_id":"2669","summary":"The protein encoded by this gene belongs to the RAD/GEM family of GTP-binding proteins. It is associated with the inner face of the plasma membrane and could play a role as a regulatory protein in receptor-mediated signal transduction. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":94249253,"end":94262350,"strand":-1,"description":"GTP binding protein overexpressed in skeletal muscle [Source:HGNC Symbol;Acc:HGNC:4234]"}, {"versioned_ensembl_gene_id":"ENSG00000282462.1","gene_symbol":"TRBV21-1","gene_name":"T-cell receptor beta variable 21-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12198]","synonyms":"TRBV211,TCRBV21S1,TCRBV10S1P","biotype":"TR_V_pseudogene","ncbi_id":"28566","summary":null,"start":142678692,"end":142679152,"strand":1,"description":"T-cell receptor beta variable 21-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12198]"}, {"versioned_ensembl_gene_id":"ENSG00000239199.1","gene_symbol":"RPL21P6","gene_name":"ribosomal protein L21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652975","summary":null,"start":55413556,"end":55414059,"strand":-1,"description":"ribosomal protein L21 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23542]"}, {"versioned_ensembl_gene_id":"ENSG00000182521.5","gene_symbol":"TBPL2","gene_name":"TATA-box binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:19841]","synonyms":"TRF3,TBP2","biotype":"protein_coding","ncbi_id":"387332","summary":null,"start":55413541,"end":55456726,"strand":-1,"description":"TATA-box binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:19841]"}, {"versioned_ensembl_gene_id":"ENSG00000104946.12","gene_symbol":"TBC1D17","gene_name":"TBC1 domain family member 17 [Source:HGNC Symbol;Acc:HGNC:25699]","synonyms":"FLJ12168","biotype":"protein_coding","ncbi_id":"79735","summary":null,"start":49877425,"end":49888749,"strand":1,"description":"TBC1 domain family member 17 [Source:HGNC Symbol;Acc:HGNC:25699]"}, {"versioned_ensembl_gene_id":"ENSG00000228849.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31557707,"end":31560476,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000125931.10","gene_symbol":"CITED1","gene_name":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 1 [Source:HGNC Symbol;Acc:HGNC:1986]","synonyms":"MSG1","biotype":"protein_coding","ncbi_id":"4435","summary":"This gene encodes a member of the CREB-binding protein/p300-interacting transactivator with Asp/Glu-rich C-terminal domain (CITED) family of proteins. The encoded protein, also known as melanocyte-specific gene 1, may function as a transcriptional coactivator and may play a role in pigmentation of melanocytes. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009]","start":72301638,"end":72307187,"strand":-1,"description":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 1 [Source:HGNC Symbol;Acc:HGNC:1986]"}, {"versioned_ensembl_gene_id":"ENSG00000101082.13","gene_symbol":"SLA2","gene_name":"Src like adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17329]","synonyms":"SLAP-2,FLJ21992,C20orf156","biotype":"protein_coding","ncbi_id":"84174","summary":"This gene encodes a member of the SLAP family of adapter proteins. The encoded protein may play an important receptor-proximal role in downregulating T and B cell-mediated responses and inhibits antigen receptor-induced calcium mobilization. This protein interacts with Cas-Br-M (murine) ecotropic retroviral transforming sequence c. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":36612318,"end":36646216,"strand":-1,"description":"Src like adaptor 2 [Source:HGNC Symbol;Acc:HGNC:17329]"}, {"versioned_ensembl_gene_id":"ENSG00000186160.4","gene_symbol":"CYP4Z1","gene_name":"cytochrome P450 family 4 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:20583]","synonyms":"CYP4A20","biotype":"protein_coding","ncbi_id":"199974","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 1p33. [provided by RefSeq, Jul 2008]","start":47067488,"end":47118319,"strand":1,"description":"cytochrome P450 family 4 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:20583]"}, {"versioned_ensembl_gene_id":"ENSG00000273635.1","gene_symbol":"AC138747.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28466463,"end":28469402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083223.17","gene_symbol":"ZCCHC6","gene_name":"zinc finger CCHC-type containing 6 [Source:HGNC Symbol;Acc:HGNC:25817]","synonyms":"PAPD6,KIAA1711,FLJ13409,TUT7","biotype":"protein_coding","ncbi_id":"79670","summary":null,"start":86287733,"end":86354454,"strand":-1,"description":"zinc finger CCHC-type containing 6 [Source:HGNC Symbol;Acc:HGNC:25817]"}, {"versioned_ensembl_gene_id":"ENSG00000143793.12","gene_symbol":"C1orf35","gene_name":"chromosome 1 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:19032]","synonyms":"MGC4174,MMTAG2","biotype":"protein_coding","ncbi_id":"79169","summary":null,"start":228100726,"end":228105411,"strand":-1,"description":"chromosome 1 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:19032]"}, {"versioned_ensembl_gene_id":"ENSG00000214336.4","gene_symbol":"FOXI3","gene_name":"forkhead box I3 [Source:HGNC Symbol;Acc:HGNC:35123]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344167","summary":null,"start":88446787,"end":88452656,"strand":-1,"description":"forkhead box I3 [Source:HGNC Symbol;Acc:HGNC:35123]"}, {"versioned_ensembl_gene_id":"ENSG00000104755.14","gene_symbol":"ADAM2","gene_name":"ADAM metallopeptidase domain 2 [Source:HGNC Symbol;Acc:HGNC:198]","synonyms":"PH30,PH-30b,FTNB,CT15","biotype":"protein_coding","ncbi_id":"2515","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded protein is a subunit of an integral sperm membrane glycoprotein called fertilin, which plays an important role in sperm-egg interactions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":39743735,"end":39838289,"strand":-1,"description":"ADAM metallopeptidase domain 2 [Source:HGNC Symbol;Acc:HGNC:198]"}, {"versioned_ensembl_gene_id":"ENSG00000229017.6","gene_symbol":"LINC01277","gene_name":"long intergenic non-protein coding RNA 1277 [Source:HGNC Symbol;Acc:HGNC:50334]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507489","summary":null,"start":142966421,"end":143038077,"strand":-1,"description":"long intergenic non-protein coding RNA 1277 [Source:HGNC Symbol;Acc:HGNC:50334]"}, {"versioned_ensembl_gene_id":"ENSG00000176248.8","gene_symbol":"ANAPC2","gene_name":"anaphase promoting complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:19989]","synonyms":"KIAA1406,APC2","biotype":"protein_coding","ncbi_id":"29882","summary":"A large protein complex, termed the anaphase-promoting complex (APC), or the cyclosome, promotes metaphase-anaphase transition by ubiquitinating its specific substrates such as mitotic cyclins and anaphase inhibitor, which are subsequently degraded by the 26S proteasome. Biochemical studies have shown that the vertebrate APC contains eight subunits. The composition of the APC is highly conserved in organisms from yeast to humans. The product of this gene is a component of the complex and shares sequence similarity with a recently identified family of proteins called cullins, which may also be involved in ubiquitin-mediated degradation. [provided by RefSeq, Jul 2008]","start":137174784,"end":137188549,"strand":-1,"description":"anaphase promoting complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:19989]"}, {"versioned_ensembl_gene_id":"ENSG00000225154.2","gene_symbol":"AL450996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47074778,"end":47075979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227192.1","gene_symbol":"AL023581.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143039425,"end":143042324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225506.2","gene_symbol":"CYP4A22-AS1","gene_name":"CYP4A22 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43715]","synonyms":"ncRNA-a3","biotype":"lincRNA","ncbi_id":"104355148","summary":null,"start":47096653,"end":47179271,"strand":-1,"description":"CYP4A22 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43715]"}, {"versioned_ensembl_gene_id":"ENSG00000159173.18","gene_symbol":"TNNI1","gene_name":"troponin I1, slow skeletal type [Source:HGNC Symbol;Acc:HGNC:11945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7135","summary":"Troponin proteins associate with tropomyosin and regulate the calcium sensitivity of the myofibril contractile apparatus of striated muscles. Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. The TnI-fast and TnI-slow genes are expressed in fast-twitch and slow-twitch skeletal muscle fibers, respectively, while the TnI-cardiac gene is expressed exclusively in cardiac muscle tissue. This gene encodes the Troponin-I-skeletal-slow-twitch protein. This gene is expressed in cardiac and skeletal muscle during early development but is restricted to slow-twitch skeletal muscle fibers in adults. The encoded protein prevents muscle contraction by inhibiting calcium-mediated conformational changes in actin-myosin complexes. [provided by RefSeq, Jul 2008]","start":201403768,"end":201429866,"strand":-1,"description":"troponin I1, slow skeletal type [Source:HGNC Symbol;Acc:HGNC:11945]"}, {"versioned_ensembl_gene_id":"ENSG00000172073.3","gene_symbol":"TEX37","gene_name":"testis expressed 37 [Source:HGNC Symbol;Acc:HGNC:26341]","synonyms":"TSC21,FLJ25369,C2orf51","biotype":"protein_coding","ncbi_id":"200523","summary":null,"start":88524651,"end":88529584,"strand":1,"description":"testis expressed 37 [Source:HGNC Symbol;Acc:HGNC:26341]"}, {"versioned_ensembl_gene_id":"ENSG00000231656.4","gene_symbol":"FAM90A18P","gene_name":"family with sequence similarity 90 member A18, pseudogene [Source:HGNC Symbol;Acc:HGNC:32266]","synonyms":"FAM90A18","biotype":"unprocessed_pseudogene","ncbi_id":"441326","summary":"FAM90A18 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7723091,"end":7726101,"strand":1,"description":"family with sequence similarity 90 member A18, pseudogene [Source:HGNC Symbol;Acc:HGNC:32266]"}, {"versioned_ensembl_gene_id":"ENSG00000225514.1","gene_symbol":"MTND1P34","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:42090]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100873219","summary":null,"start":47164510,"end":47165920,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:42090]"}, {"versioned_ensembl_gene_id":"ENSG00000148704.12","gene_symbol":"VAX1","gene_name":"ventral anterior homeobox 1 [Source:HGNC Symbol;Acc:HGNC:12660]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11023","summary":"This gene encodes a homeo-domain containing protein from a class of homeobox transcription factors which are conserved in vertebrates. Genes of this family are involved in the regulation of body development and morphogenesis. The most conserved genes, called HOX genes are found in special gene clusters. This gene belongs to the VAX subfamily and lies in the vicinity of the EMX homeobox gene family. Another member of VAX family is located on chromosome 2. The encoded protein may play an important role in the development of anterior ventral forebrain and visual system. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":117128521,"end":117138301,"strand":-1,"description":"ventral anterior homeobox 1 [Source:HGNC Symbol;Acc:HGNC:12660]"}, {"versioned_ensembl_gene_id":"ENSG00000224805.2","gene_symbol":"LINC00853","gene_name":"long intergenic non-protein coding RNA 853 [Source:HGNC Symbol;Acc:HGNC:43716]","synonyms":"PDZK1IP1-AS1,ncRNA-a4","biotype":"antisense_RNA","ncbi_id":"100874253","summary":null,"start":47179250,"end":47180339,"strand":1,"description":"long intergenic non-protein coding RNA 853 [Source:HGNC Symbol;Acc:HGNC:43716]"}, {"versioned_ensembl_gene_id":"ENSG00000140682.18","gene_symbol":"TGFB1I1","gene_name":"transforming growth factor beta 1 induced transcript 1 [Source:HGNC Symbol;Acc:HGNC:11767]","synonyms":"TSC-5,Hic-5,ARA55","biotype":"protein_coding","ncbi_id":"7041","summary":"This gene encodes a coactivator of the androgen receptor, a transcription factor which is activated by androgen and has a key role in male sexual differentiation. The encoded protein is thought to regulate androgen receptor activity and may have a role to play in the treatment of prostate cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":31471585,"end":31477960,"strand":1,"description":"transforming growth factor beta 1 induced transcript 1 [Source:HGNC Symbol;Acc:HGNC:11767]"}, {"versioned_ensembl_gene_id":"ENSG00000231969.1","gene_symbol":"AC007364.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149587196,"end":149848233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227688.2","gene_symbol":"HNRNPA3P2","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16605]","synonyms":"HNRPA3P2,HNRPA3P,dJ977B1.2","biotype":"unprocessed_pseudogene","ncbi_id":"170526","summary":null,"start":36620403,"end":36621423,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16605]"}, {"versioned_ensembl_gene_id":"ENSG00000162365.11","gene_symbol":"CYP4A22","gene_name":"cytochrome P450 family 4 subfamily A member 22 [Source:HGNC Symbol;Acc:HGNC:20575]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284541","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 1p33. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":47137435,"end":47149741,"strand":1,"description":"cytochrome P450 family 4 subfamily A member 22 [Source:HGNC Symbol;Acc:HGNC:20575]"}, {"versioned_ensembl_gene_id":"ENSG00000273085.1","gene_symbol":"AC113331.2","gene_name":null,"synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":null,"summary":null,"start":5069572,"end":5070497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166448.14","gene_symbol":"TMEM130","gene_name":"transmembrane protein 130 [Source:HGNC Symbol;Acc:HGNC:25429]","synonyms":"FLJ42643,DKFZp761L1417","biotype":"protein_coding","ncbi_id":"222865","summary":null,"start":98846488,"end":98870771,"strand":-1,"description":"transmembrane protein 130 [Source:HGNC Symbol;Acc:HGNC:25429]"}, {"versioned_ensembl_gene_id":"ENSG00000168288.12","gene_symbol":"MMADHC","gene_name":"methylmalonic aciduria and homocystinuria, cblD type [Source:HGNC Symbol;Acc:HGNC:25221]","synonyms":"CL25022,cblD,C2orf25","biotype":"protein_coding","ncbi_id":"27249","summary":"This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008]","start":149569634,"end":149587816,"strand":-1,"description":"methylmalonic aciduria and homocystinuria, cblD type [Source:HGNC Symbol;Acc:HGNC:25221]"}, {"versioned_ensembl_gene_id":"ENSG00000119684.15","gene_symbol":"MLH3","gene_name":"mutL homolog 3 [Source:HGNC Symbol;Acc:HGNC:7128]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27030","summary":"This gene is a member of the MutL-homolog (MLH) family of DNA mismatch repair (MMR) genes. MLH genes are implicated in maintaining genomic integrity during DNA replication and after meiotic recombination. The protein encoded by this gene functions as a heterodimer with other family members. Somatic mutations in this gene frequently occur in tumors exhibiting microsatellite instability, and germline mutations have been linked to hereditary nonpolyposis colorectal cancer type 7 (HNPCC7). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]","start":75013764,"end":75051532,"strand":-1,"description":"mutL homolog 3 [Source:HGNC Symbol;Acc:HGNC:7128]"}, {"versioned_ensembl_gene_id":"ENSG00000118707.9","gene_symbol":"TGIF2","gene_name":"TGFB induced factor homeobox 2 [Source:HGNC Symbol;Acc:HGNC:15764]","synonyms":null,"biotype":"protein_coding","ncbi_id":"60436","summary":"The protein encoded by this gene is a DNA-binding homeobox protein and a transcriptional repressor, which appears to repress transcription by recruiting histone deacetylases to TGF beta-responsive genes. This gene is amplified and over-expressed in some ovarian cancers. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. Read-through transcription also exists between this gene and the neighboring downstream C20orf24 (chromosome 20 open reading frame 24) gene. [provided by RefSeq, Dec 2010]","start":36573488,"end":36593950,"strand":1,"description":"TGFB induced factor homeobox 2 [Source:HGNC Symbol;Acc:HGNC:15764]"}, {"versioned_ensembl_gene_id":"ENSG00000237354.1","gene_symbol":"OR52S1P","gene_name":"olfactory receptor family 52 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14805]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79521","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5076130,"end":5077066,"strand":-1,"description":"olfactory receptor family 52 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14805]"}, {"versioned_ensembl_gene_id":"ENSG00000258413.1","gene_symbol":"AL158801.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55262767,"end":55272075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284726.1","gene_symbol":"AL109936.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23297797,"end":23302866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271849.1","gene_symbol":"AC012603.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109687802,"end":109688329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226157.1","gene_symbol":"OR52E3P","gene_name":"olfactory receptor family 52 subfamily E member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14793]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79533","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5092676,"end":5093611,"strand":1,"description":"olfactory receptor family 52 subfamily E member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14793]"}, {"versioned_ensembl_gene_id":"ENSG00000282036.1","gene_symbol":"TRBV22-1","gene_name":"T-cell receptor beta variable 22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12200]","synonyms":"TRBV22,TCRBV29S1P,TCRBV22S1","biotype":"TR_V_pseudogene","ncbi_id":"28565","summary":null,"start":142683514,"end":142683964,"strand":1,"description":"T-cell receptor beta variable 22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12200]"}, {"versioned_ensembl_gene_id":"ENSG00000203560.3","gene_symbol":"OR52J1P","gene_name":"olfactory receptor family 52 subfamily J member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14760]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79302","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5104153,"end":5105084,"strand":1,"description":"olfactory receptor family 52 subfamily J member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14760]"}, {"versioned_ensembl_gene_id":"ENSG00000165105.9","gene_symbol":"RASEF","gene_name":"RAS and EF-hand domain containing [Source:HGNC Symbol;Acc:HGNC:26464]","synonyms":"RAB45,FLJ31614","biotype":"protein_coding","ncbi_id":"158158","summary":"This gene is a member of the Rab family of GTPases that are involved in regulation of membrane traffic. The encoded protein contains an N-terminal EF-hand domain, a coiled-coil motif and a C-terminal Rab domain. A potential role as tumor suppressor has been indicated for this gene. [provided by RefSeq, Nov 2012]","start":82979585,"end":83063177,"strand":-1,"description":"RAS and EF-hand domain containing [Source:HGNC Symbol;Acc:HGNC:26464]"}, {"versioned_ensembl_gene_id":"ENSG00000136100.12","gene_symbol":"VPS36","gene_name":"vacuolar protein sorting 36 homolog [Source:HGNC Symbol;Acc:HGNC:20312]","synonyms":"Eap45,CGI-145,C13orf9","biotype":"protein_coding","ncbi_id":"51028","summary":"This gene encodes a protein that is a subunit of the endosomal sorting complex required for transport II (ESCRT-II). This protein complex functions in sorting of ubiquitinated membrane proteins during endocytosis. A similar protein complex in rat is associated with RNA polymerase elongation factor II. [provided by RefSeq, Aug 2013]","start":52412602,"end":52450628,"strand":-1,"description":"vacuolar protein sorting 36 homolog [Source:HGNC Symbol;Acc:HGNC:20312]"}, {"versioned_ensembl_gene_id":"ENSG00000186871.6","gene_symbol":"ERCC6L","gene_name":"ERCC excision repair 6 like, spindle assembly checkpoint helicase [Source:HGNC Symbol;Acc:HGNC:20794]","synonyms":"RAD26L,PICH,FLJ20105","biotype":"protein_coding","ncbi_id":"54821","summary":"This gene encodes a member of the SWItch/Sucrose Non-Fermentable (SWI/SNF2) family of proteins, and contains a SNF2-like ATPase domain and a PICH family domain. One distinguishing feature of this SWI/SNF protein family member is that during interphase, the protein is excluded from the nucleus, and only associates with chromatin after the nuclear envelope has broken down. This protein is a DNA translocase that is thought to bind double-stranded DNA that is exposed to stretching forces, such as those exerted by the mitotic spindle. This protein associates with ribosomal DNA and ultra-fine DNA bridges (UFBs), fine structures that connect sister chromatids during anaphase at some sites such as fragile sites, telomeres and centromeres. This gene is required for the faithful segregation of sister chromatids during mitosis, and the ATPase activity of this protein required for the resolution of UFBs before cytokinesis. [provided by RefSeq, May 2017]","start":72204657,"end":72239047,"strand":-1,"description":"ERCC excision repair 6 like, spindle assembly checkpoint helicase [Source:HGNC Symbol;Acc:HGNC:20794]"}, {"versioned_ensembl_gene_id":"ENSG00000233427.1","gene_symbol":"AL009181.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28870483,"end":28877336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116329.10","gene_symbol":"OPRD1","gene_name":"opioid receptor delta 1 [Source:HGNC Symbol;Acc:HGNC:8153]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4985","summary":null,"start":28812142,"end":28871267,"strand":1,"description":"opioid receptor delta 1 [Source:HGNC Symbol;Acc:HGNC:8153]"}, {"versioned_ensembl_gene_id":"ENSG00000183704.7","gene_symbol":"SLC9B1P1","gene_name":"solute carrier family 9 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37492]","synonyms":"NHEDC1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100128190","summary":null,"start":11340579,"end":11385687,"strand":-1,"description":"solute carrier family 9 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37492]"}, {"versioned_ensembl_gene_id":"ENSG00000253417.5","gene_symbol":"LINC02159","gene_name":"long intergenic non-protein coding RNA 2159 [Source:HGNC Symbol;Acc:HGNC:27749]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285629","summary":null,"start":160931778,"end":160938626,"strand":-1,"description":"long intergenic non-protein coding RNA 2159 [Source:HGNC Symbol;Acc:HGNC:27749]"}, {"versioned_ensembl_gene_id":"ENSG00000251013.1","gene_symbol":"GAPDHP62","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:4156]","synonyms":"GAPDL7,GAPDHL7","biotype":"processed_pseudogene","ncbi_id":"100128961","summary":null,"start":100550724,"end":100551713,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:4156]"}, {"versioned_ensembl_gene_id":"ENSG00000186106.11","gene_symbol":"ANKRD46","gene_name":"ankyrin repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:27229]","synonyms":null,"biotype":"protein_coding","ncbi_id":"157567","summary":"This gene encodes a protein containing multiple ankyrin repeats. Ankyrin domains function in protein-protein interactions in a variety of cellular processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":100509752,"end":100559784,"strand":-1,"description":"ankyrin repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:27229]"}, {"versioned_ensembl_gene_id":"ENSG00000204673.10","gene_symbol":"AKT1S1","gene_name":"AKT1 substrate 1 [Source:HGNC Symbol;Acc:HGNC:28426]","synonyms":"PRAS40,MGC2865,Lobe","biotype":"protein_coding","ncbi_id":"84335","summary":"AKT1S1 is a proline-rich substrate of AKT (MIM 164730) that binds 14-3-3 protein (see YWHAH, MIM 113508) when phosphorylated (Kovacina et al., 2003 [PubMed 12524439]).[supplied by OMIM, Mar 2008]","start":49869033,"end":49878459,"strand":-1,"description":"AKT1 substrate 1 [Source:HGNC Symbol;Acc:HGNC:28426]"}, {"versioned_ensembl_gene_id":"ENSG00000187713.6","gene_symbol":"TMEM203","gene_name":"transmembrane protein 203 [Source:HGNC Symbol;Acc:HGNC:28217]","synonyms":"MGC14327,HBEBP1","biotype":"protein_coding","ncbi_id":"94107","summary":null,"start":137204082,"end":137205638,"strand":-1,"description":"transmembrane protein 203 [Source:HGNC Symbol;Acc:HGNC:28217]"}, {"versioned_ensembl_gene_id":"ENSG00000278023.5","gene_symbol":"RDM1","gene_name":"RAD52 motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19950]","synonyms":"RAD52B,MGC33977","biotype":"protein_coding","ncbi_id":"201299","summary":"This gene encodes a protein involved in the cellular response to cisplatin, a drug commonly used in chemotherapy. The protein encoded by this gene contains two motifs: a motif found in RAD52, a protein that functions in DNA double-strand breaks and homologous recombination, and an RNA recognition motif (RRM) that is not found in RAD52. The RAD52 motif region in RAD52 is important for protein function and may be involved in DNA binding or oligomerization. Alternatively spliced transcript variants encoding different isoforms have been reported. [provided by RefSeq, Jul 2008]","start":35918066,"end":35930773,"strand":-1,"description":"RAD52 motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19950]"}, {"versioned_ensembl_gene_id":"ENSG00000204581.2","gene_symbol":"ACOXL-AS1","gene_name":"ACOXL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41112]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"400997","summary":null,"start":111098345,"end":111115588,"strand":-1,"description":"ACOXL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41112]"}, {"versioned_ensembl_gene_id":"ENSG00000205494.9","gene_symbol":"OR52A4P","gene_name":"olfactory receptor family 52 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:19579]","synonyms":"OR52A4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390053","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. Although originally considered to be a functional olfactory receptor, this family member is now considered to be pseudogene due to the presence of a C-terminal frameshift compared to other family members; this is also consistent with the Classifier for Olfactory Receptor Pseudogenes (CORP), as described in PMID:16939646. [provided by RefSeq, Jun 2011]","start":5120621,"end":5124513,"strand":-1,"description":"olfactory receptor family 52 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:19579]"}, {"versioned_ensembl_gene_id":"ENSG00000176058.11","gene_symbol":"TPRN","gene_name":"taperin [Source:HGNC Symbol;Acc:HGNC:26894]","synonyms":"FLJ90254,DFNB79,C9orf75","biotype":"protein_coding","ncbi_id":"286262","summary":"This locus encodes a sensory epithelial protein. It was defined by linkage analysis in three Pakistani families to lie between D9S1818 (centromeric) and D9SH6 (telomeric). Mutations at this locus have been associated with autosomal recessive deafness. [provided by RefSeq, Oct 2010]","start":137191617,"end":137204193,"strand":-1,"description":"taperin [Source:HGNC Symbol;Acc:HGNC:26894]"}, {"versioned_ensembl_gene_id":"ENSG00000282449.1","gene_symbol":"TRBV23-1","gene_name":"T-cell receptor beta variable 23-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12201]","synonyms":"TCRBV19S1P,TRBV231,TCRBV23S1","biotype":"TR_V_gene","ncbi_id":"28564","summary":null,"start":142687733,"end":142688229,"strand":1,"description":"T-cell receptor beta variable 23-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12201]"}, {"versioned_ensembl_gene_id":"ENSG00000171944.2","gene_symbol":"OR52A5","gene_name":"olfactory receptor family 52 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:19580]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390054","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5128776,"end":5138356,"strand":-1,"description":"olfactory receptor family 52 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:19580]"}, {"versioned_ensembl_gene_id":"ENSG00000236925.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31562695,"end":31564662,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000182070.5","gene_symbol":"OR52A1","gene_name":"olfactory receptor family 52 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8318]","synonyms":"HPFH1OR","biotype":"protein_coding","ncbi_id":"23538","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5143219,"end":5154757,"strand":-1,"description":"olfactory receptor family 52 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8318]"}, {"versioned_ensembl_gene_id":"ENSG00000176748.5","gene_symbol":"OR52Z1","gene_name":"olfactory receptor family 52 subfamily Z member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19596]","synonyms":"OR52Z1P","biotype":"polymorphic_pseudogene","ncbi_id":"283110","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":5177714,"end":5178610,"strand":-1,"description":"olfactory receptor family 52 subfamily Z member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19596]"}, {"versioned_ensembl_gene_id":"ENSG00000281946.1","gene_symbol":"AC138749.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28506596,"end":28506797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230184.1","gene_symbol":"SMYD3-IT1","gene_name":"SMYD3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41406]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478975","summary":null,"start":246321663,"end":246322438,"strand":-1,"description":"SMYD3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41406]"}, {"versioned_ensembl_gene_id":"ENSG00000151657.11","gene_symbol":"KIN","gene_name":"Kin17 DNA and RNA binding protein [Source:HGNC Symbol;Acc:HGNC:6327]","synonyms":"Rts2,KIN17","biotype":"protein_coding","ncbi_id":"22944","summary":"The protein encoded by this gene is a nuclear protein that forms intranuclear foci during proliferation and is redistributed in the nucleoplasm during the cell cycle. Short-wave ultraviolet light provokes the relocalization of the protein, suggesting its participation in the cellular response to DNA damage. Originally selected based on protein-binding with RecA antibodies, the mouse protein presents a limited similarity with a functional domain of the bacterial RecA protein, a characteristic shared by this human ortholog. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":7750962,"end":7787981,"strand":-1,"description":"Kin17 DNA and RNA binding protein [Source:HGNC Symbol;Acc:HGNC:6327]"}, {"versioned_ensembl_gene_id":"ENSG00000226301.3","gene_symbol":"PDCL3P1","gene_name":"phosducin-like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392225","summary":null,"start":60387262,"end":60387995,"strand":1,"description":"phosducin-like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31826]"}, {"versioned_ensembl_gene_id":"ENSG00000225721.5","gene_symbol":"AL592166.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44759037,"end":44775810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167549.18","gene_symbol":"CORO6","gene_name":"coronin 6 [Source:HGNC Symbol;Acc:HGNC:21356]","synonyms":"FLJ14871","biotype":"protein_coding","ncbi_id":"84940","summary":null,"start":29614756,"end":29622907,"strand":-1,"description":"coronin 6 [Source:HGNC Symbol;Acc:HGNC:21356]"}, {"versioned_ensembl_gene_id":"ENSG00000153531.13","gene_symbol":"ADPRHL1","gene_name":"ADP-ribosylhydrolase like 1 [Source:HGNC Symbol;Acc:HGNC:21303]","synonyms":"ARH2","biotype":"protein_coding","ncbi_id":"113622","summary":"ADP-ribosylation is a reversible posttranslational modification used to regulate protein function. ADP-ribosyltransferases (see ART1; MIM 601625) transfer ADP-ribose from NAD+ to the target protein, and ADP-ribosylhydrolases, such as ADPRHL1, reverse the reaction (Glowacki et al., 2002 [PubMed 12070318]).[supplied by OMIM, Mar 2008]","start":113399610,"end":113453524,"strand":-1,"description":"ADP-ribosylhydrolase like 1 [Source:HGNC Symbol;Acc:HGNC:21303]"}, {"versioned_ensembl_gene_id":"ENSG00000277687.1","gene_symbol":"AL139407.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":118692361,"end":118693535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251221.1","gene_symbol":"LINC01337","gene_name":"long intergenic non-protein coding RNA 1337 [Source:HGNC Symbol;Acc:HGNC:50546]","synonyms":"TCONS_00009713","biotype":"lincRNA","ncbi_id":"103689917","summary":null,"start":80608623,"end":80622524,"strand":-1,"description":"long intergenic non-protein coding RNA 1337 [Source:HGNC Symbol;Acc:HGNC:50546]"}, {"versioned_ensembl_gene_id":"ENSG00000256752.1","gene_symbol":"HPRT1P3","gene_name":"hypoxanthine phosphoribosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:5161]","synonyms":"HPRTP4,HPRTP3","biotype":"processed_pseudogene","ncbi_id":"3255","summary":null,"start":93998643,"end":93999218,"strand":-1,"description":"hypoxanthine phosphoribosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:5161]"}, {"versioned_ensembl_gene_id":"ENSG00000255995.1","gene_symbol":"AP002795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93991346,"end":93991429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178538.9","gene_symbol":"CA8","gene_name":"carbonic anhydrase 8 [Source:HGNC Symbol;Acc:HGNC:1382]","synonyms":"CARP,CALS","biotype":"protein_coding","ncbi_id":"767","summary":"The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":60187347,"end":60281412,"strand":-1,"description":"carbonic anhydrase 8 [Source:HGNC Symbol;Acc:HGNC:1382]"}, {"versioned_ensembl_gene_id":"ENSG00000267278.5","gene_symbol":"MAP3K14-AS1","gene_name":"MAP3K14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44359]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100133991","summary":null,"start":45247925,"end":45268630,"strand":1,"description":"MAP3K14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44359]"}, {"versioned_ensembl_gene_id":"ENSG00000162869.15","gene_symbol":"PPP1R21","gene_name":"protein phosphatase 1 regulatory subunit 21 [Source:HGNC Symbol;Acc:HGNC:30595]","synonyms":"KLRAQ1,FLJ16566,CCDC128","biotype":"protein_coding","ncbi_id":"129285","summary":null,"start":48440598,"end":48515391,"strand":1,"description":"protein phosphatase 1 regulatory subunit 21 [Source:HGNC Symbol;Acc:HGNC:30595]"}, {"versioned_ensembl_gene_id":"ENSG00000197756.9","gene_symbol":"RPL37A","gene_name":"ribosomal protein L37a [Source:HGNC Symbol;Acc:HGNC:10348]","synonyms":"L37A","biotype":"protein_coding","ncbi_id":"6168","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L37AE family of ribosomal proteins. It is located in the cytoplasm. The protein contains a C4-type zinc finger-like domain. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":216498189,"end":216579180,"strand":1,"description":"ribosomal protein L37a [Source:HGNC Symbol;Acc:HGNC:10348]"}, {"versioned_ensembl_gene_id":"ENSG00000253381.1","gene_symbol":"AC087518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40104169,"end":40107935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278369.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2b,p58,CD158B2,cl-6,nkat2,nkat2a","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738530,"end":54753070,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000254775.1","gene_symbol":"AC021393.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60049587,"end":60074715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276728.1","gene_symbol":"AC142472.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45146730,"end":45148470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251058.1","gene_symbol":"AC010181.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140461000,"end":140462825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211941.3","gene_symbol":"IGHV3-11","gene_name":"immunoglobulin heavy variable 3-11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5580]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28450","summary":null,"start":106116635,"end":106117204,"strand":-1,"description":"immunoglobulin heavy variable 3-11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5580]"}, {"versioned_ensembl_gene_id":"ENSG00000277738.1","gene_symbol":"AC126175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91634887,"end":91635644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282651.2","gene_symbol":"AC247036.6","gene_name":"Immunoglobulin heavy variable 5-10-1 [Source:UniProtKB/Swiss-Prot;Acc:A0A0J9YXX1]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106107972,"end":106108464,"strand":-1,"description":"Immunoglobulin heavy variable 5-10-1 [Source:UniProtKB/Swiss-Prot;Acc:A0A0J9YXX1]"}, {"versioned_ensembl_gene_id":"ENSG00000000457.13","gene_symbol":"SCYL3","gene_name":"SCY1 like pseudokinase 3 [Source:HGNC Symbol;Acc:HGNC:19285]","synonyms":"PACE1,PACE-1","biotype":"protein_coding","ncbi_id":"57147","summary":"This gene encodes a protein with a kinase domain and four HEAT repeats. The encoded protein interacts with the C-terminal domain of ezrin, an ERM protein, and may play a role in cell adhesion and migration. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Jun 2012]","start":169849631,"end":169894267,"strand":-1,"description":"SCY1 like pseudokinase 3 [Source:HGNC Symbol;Acc:HGNC:19285]"}, {"versioned_ensembl_gene_id":"ENSG00000211937.3","gene_symbol":"IGHV2-5","gene_name":"immunoglobulin heavy variable 2-5 [Source:HGNC Symbol;Acc:HGNC:5576]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28457","summary":null,"start":106037902,"end":106038365,"strand":-1,"description":"immunoglobulin heavy variable 2-5 [Source:HGNC Symbol;Acc:HGNC:5576]"}, {"versioned_ensembl_gene_id":"ENSG00000140264.19","gene_symbol":"SERF2","gene_name":"small EDRK-rich factor 2 [Source:HGNC Symbol;Acc:HGNC:10757]","synonyms":"FAM2C,4F5REL,HsT17089,H4F5rel","biotype":"protein_coding","ncbi_id":"10169","summary":null,"start":43777087,"end":43802589,"strand":1,"description":"small EDRK-rich factor 2 [Source:HGNC Symbol;Acc:HGNC:10757]"}, {"versioned_ensembl_gene_id":"ENSG00000182575.7","gene_symbol":"NXPH3","gene_name":"neurexophilin 3 [Source:HGNC Symbol;Acc:HGNC:8077]","synonyms":"NPH3","biotype":"protein_coding","ncbi_id":"11248","summary":null,"start":49575858,"end":49583827,"strand":1,"description":"neurexophilin 3 [Source:HGNC Symbol;Acc:HGNC:8077]"}, {"versioned_ensembl_gene_id":"ENSG00000224536.2","gene_symbol":"AC096677.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201507241,"end":201534784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183426.16","gene_symbol":"NPIPA1","gene_name":"nuclear pore complex interacting protein family member A1 [Source:HGNC Symbol;Acc:HGNC:7909]","synonyms":"NPIP,morpheus","biotype":"protein_coding","ncbi_id":"9284","summary":null,"start":14922802,"end":14952060,"strand":1,"description":"nuclear pore complex interacting protein family member A1 [Source:HGNC Symbol;Acc:HGNC:7909]"}, {"versioned_ensembl_gene_id":"ENSG00000164626.8","gene_symbol":"KCNK5","gene_name":"potassium two pore domain channel subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:6280]","synonyms":"TASK-2,K2p5.1","biotype":"protein_coding","ncbi_id":"8645","summary":"This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The message for this gene is mainly expressed in the cortical distal tubules and collecting ducts of the kidney. The protein is highly sensitive to external pH and this, in combination with its expression pattern, suggests it may play an important role in renal potassium transport. [provided by RefSeq, Jul 2008]","start":39188973,"end":39229450,"strand":-1,"description":"potassium two pore domain channel subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:6280]"}, {"versioned_ensembl_gene_id":"ENSG00000119707.13","gene_symbol":"RBM25","gene_name":"RNA binding motif protein 25 [Source:HGNC Symbol;Acc:HGNC:23244]","synonyms":"Snu71,S164,RNPC7,NET52,fSAP94","biotype":"protein_coding","ncbi_id":"58517","summary":null,"start":73058436,"end":73123898,"strand":1,"description":"RNA binding motif protein 25 [Source:HGNC Symbol;Acc:HGNC:23244]"}, {"versioned_ensembl_gene_id":"ENSG00000253780.1","gene_symbol":"IGHVIII-2-1","gene_name":"immunoglobulin heavy variable (III)-2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5695]","synonyms":"IGHV(III)-2-1","biotype":"IG_V_pseudogene","ncbi_id":"28355","summary":null,"start":106001534,"end":106001824,"strand":-1,"description":"immunoglobulin heavy variable (III)-2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5695]"}, {"versioned_ensembl_gene_id":"ENSG00000148386.9","gene_symbol":"LCN9","gene_name":"lipocalin 9 [Source:HGNC Symbol;Acc:HGNC:17442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392399","summary":"Members of the lipocalin family, such as LCN9, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":135663322,"end":135666422,"strand":1,"description":"lipocalin 9 [Source:HGNC Symbol;Acc:HGNC:17442]"}, {"versioned_ensembl_gene_id":"ENSG00000254630.1","gene_symbol":"AP001922.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75635883,"end":75638587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244575.3","gene_symbol":"IGKV1-27","gene_name":"immunoglobulin kappa variable 1-27 [Source:HGNC Symbol;Acc:HGNC:5735]","synonyms":"IGKV127,A20","biotype":"IG_V_gene","ncbi_id":"28935","summary":null,"start":89213423,"end":89213928,"strand":-1,"description":"immunoglobulin kappa variable 1-27 [Source:HGNC Symbol;Acc:HGNC:5735]"}, {"versioned_ensembl_gene_id":"ENSG00000270904.1","gene_symbol":"AC008385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151319422,"end":151319776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203930.10","gene_symbol":"LINC00632","gene_name":"long intergenic non-protein coding RNA 632 [Source:HGNC Symbol;Acc:HGNC:27865]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286411","summary":null,"start":140709767,"end":140772679,"strand":1,"description":"long intergenic non-protein coding RNA 632 [Source:HGNC Symbol;Acc:HGNC:27865]"}, {"versioned_ensembl_gene_id":"ENSG00000148399.12","gene_symbol":"DPH7","gene_name":"diphthamide biosynthesis 7 [Source:HGNC Symbol;Acc:HGNC:25199]","synonyms":"WDR85,RRT2,FLJ90634,C9orf112","biotype":"protein_coding","ncbi_id":"92715","summary":"Diphthamide is a post-translationally modified histidine residue present in elongation factor 2, and is the target of diphtheria toxin. This gene encodes a protein that contains a WD-40 domain, and is thought to be involved in diphthamide biosynthesis. A similar protein in yeast functions as a methylesterase, converting methylated diphthine to diphthine, which can then undergo amidation to produce diphthamide. [provided by RefSeq, Oct 2016]","start":137554904,"end":137578935,"strand":-1,"description":"diphthamide biosynthesis 7 [Source:HGNC Symbol;Acc:HGNC:25199]"}, {"versioned_ensembl_gene_id":"ENSG00000240130.1","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"processed_transcript","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29422486,"end":29431843,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000253846.2","gene_symbol":"PCDHGA10","gene_name":"protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:HGNC:8697]","synonyms":"PCDH-GAMMA-A10","biotype":"protein_coding","ncbi_id":"56106","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141412987,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:HGNC:8697]"}, {"versioned_ensembl_gene_id":"ENSG00000249435.1","gene_symbol":"AC022137.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53426019,"end":53426499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253910.2","gene_symbol":"PCDHGB2","gene_name":"protocadherin gamma subfamily B, 2 [Source:HGNC Symbol;Acc:HGNC:8709]","synonyms":"PCDH-GAMMA-B2","biotype":"protein_coding","ncbi_id":"56103","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141360042,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 2 [Source:HGNC Symbol;Acc:HGNC:8709]"}, {"versioned_ensembl_gene_id":"ENSG00000273557.1","gene_symbol":"AC008781.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":141468465,"end":141471528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213799.11","gene_symbol":"ZNF845","gene_name":"zinc finger protein 845 [Source:HGNC Symbol;Acc:HGNC:25112]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91664","summary":null,"start":53333749,"end":53354869,"strand":1,"description":"zinc finger protein 845 [Source:HGNC Symbol;Acc:HGNC:25112]"}, {"versioned_ensembl_gene_id":"ENSG00000264138.1","gene_symbol":"AC024267.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28848860,"end":28849592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166578.9","gene_symbol":"IQCD","gene_name":"IQ motif containing D [Source:HGNC Symbol;Acc:HGNC:25168]","synonyms":"DRC10,CFAP84","biotype":"protein_coding","ncbi_id":"115811","summary":null,"start":113195441,"end":113221094,"strand":-1,"description":"IQ motif containing D [Source:HGNC Symbol;Acc:HGNC:25168]"}, {"versioned_ensembl_gene_id":"ENSG00000226928.1","gene_symbol":"RPS14P4","gene_name":"ribosomal protein S14 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36419]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132382","summary":null,"start":111295629,"end":111296046,"strand":-1,"description":"ribosomal protein S14 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36419]"}, {"versioned_ensembl_gene_id":"ENSG00000172965.14","gene_symbol":"MIR4435-2HG","gene_name":"MIR4435-2 host gene [Source:HGNC Symbol;Acc:HGNC:35163]","synonyms":"LINC00978,AK001796,AGD2,MORRBID,MIR4435-1HG,lncRNA-AWPPH","biotype":"lincRNA","ncbi_id":"541471","summary":null,"start":111196350,"end":111495100,"strand":-1,"description":"MIR4435-2 host gene [Source:HGNC Symbol;Acc:HGNC:35163]"}, {"versioned_ensembl_gene_id":"ENSG00000204435.13","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb1,Ckb2","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31665236,"end":31670343,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000173559.12","gene_symbol":"NABP1","gene_name":"nucleic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:26232]","synonyms":"SSB2,SOSS-B2,OBFC2A,MGC111163,hSSB2,FLJ22833,FLJ13624,DKFZp667M1322","biotype":"protein_coding","ncbi_id":"64859","summary":"Single-stranded DNA (ssDNA)-binding proteins, such as OBFC2A, are ubiquitous and essential for a variety of DNA metabolic processes, including replication, recombination, and detection and repair of damage (Richard et al., 2008 [PubMed 18449195]).[supplied by OMIM, Jun 2008]","start":191678068,"end":191696659,"strand":1,"description":"nucleic acid binding protein 1 [Source:HGNC Symbol;Acc:HGNC:26232]"}, {"versioned_ensembl_gene_id":"ENSG00000160345.12","gene_symbol":"C9orf116","gene_name":"chromosome 9 open reading frame 116 [Source:HGNC Symbol;Acc:HGNC:28435]","synonyms":"RbEST47,PIERCE1,MGC29761","biotype":"protein_coding","ncbi_id":"138162","summary":null,"start":135495181,"end":135501734,"strand":-1,"description":"chromosome 9 open reading frame 116 [Source:HGNC Symbol;Acc:HGNC:28435]"}, {"versioned_ensembl_gene_id":"ENSG00000188211.8","gene_symbol":"NCR3LG1","gene_name":"natural killer cell cytotoxicity receptor 3 ligand 1 [Source:HGNC Symbol;Acc:HGNC:42400]","synonyms":"DKFZp686O24166,B7-H6","biotype":"protein_coding","ncbi_id":"374383","summary":"B7H6 belongs to the B7 family (see MIM 605402) and is selectively expressed on tumor cells. Interaction of B7H6 with NKp30 (NCR3; MIM 611550) results in natural killer (NK) cell activation and cytotoxicity (Brandt et al., 2009 [PubMed 19528259]).[supplied by OMIM, Jan 2011]","start":17351726,"end":17377341,"strand":1,"description":"natural killer cell cytotoxicity receptor 3 ligand 1 [Source:HGNC Symbol;Acc:HGNC:42400]"}, {"versioned_ensembl_gene_id":"ENSG00000229093.1","gene_symbol":"OR51AB1P","gene_name":"olfactory receptor family 51 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31278]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403265","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5291761,"end":5292380,"strand":-1,"description":"olfactory receptor family 51 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31278]"}, {"versioned_ensembl_gene_id":"ENSG00000229036.7","gene_symbol":"VDAC1P8","gene_name":"voltage dependent anion channel 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37483]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100310840","summary":null,"start":143490424,"end":143506406,"strand":1,"description":"voltage dependent anion channel 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37483]"}, {"versioned_ensembl_gene_id":"ENSG00000211598.2","gene_symbol":"IGKV4-1","gene_name":"immunoglobulin kappa variable 4-1 [Source:HGNC Symbol;Acc:HGNC:5834]","synonyms":"IGKV41,B3","biotype":"IG_V_gene","ncbi_id":"28908","summary":null,"start":88885397,"end":88886153,"strand":1,"description":"immunoglobulin kappa variable 4-1 [Source:HGNC Symbol;Acc:HGNC:5834]"}, {"versioned_ensembl_gene_id":"ENSG00000269621.1","gene_symbol":"AL589765.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151755541,"end":151759911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236940.1","gene_symbol":"AL589765.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151757659,"end":151758442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244076.1","gene_symbol":"AC026410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80315671,"end":80315826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231447.1","gene_symbol":"AC244102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152746817,"end":152747762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184188.6","gene_symbol":"AC026410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80299678,"end":80302847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156535.13","gene_symbol":"CD109","gene_name":"CD109 molecule [Source:HGNC Symbol;Acc:HGNC:21685]","synonyms":"FLJ38569,DKFZp762L1111,CPAMD7","biotype":"protein_coding","ncbi_id":"135228","summary":"This gene encodes a glycosyl phosphatidylinositol (GPI)-linked glycoprotein that localizes to the surface of platelets, activated T-cells, and endothelial cells. The protein binds to and negatively regulates signalling by transforming growth factor beta (TGF-beta). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":73695785,"end":73828316,"strand":1,"description":"CD109 molecule [Source:HGNC Symbol;Acc:HGNC:21685]"}, {"versioned_ensembl_gene_id":"ENSG00000227123.1","gene_symbol":"RPL12P44","gene_name":"ribosomal protein L12 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:44603]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419392","summary":null,"start":44937673,"end":44938482,"strand":1,"description":"ribosomal protein L12 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:44603]"}, {"versioned_ensembl_gene_id":"ENSG00000154133.14","gene_symbol":"ROBO4","gene_name":"roundabout guidance receptor 4 [Source:HGNC Symbol;Acc:HGNC:17985]","synonyms":"ECSM4,MRB,FLJ20798","biotype":"protein_coding","ncbi_id":"54538","summary":null,"start":124883691,"end":124898500,"strand":-1,"description":"roundabout guidance receptor 4 [Source:HGNC Symbol;Acc:HGNC:17985]"}, {"versioned_ensembl_gene_id":"ENSG00000268842.1","gene_symbol":"AC092070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53162428,"end":53163563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143369.14","gene_symbol":"ECM1","gene_name":"extracellular matrix protein 1 [Source:HGNC Symbol;Acc:HGNC:3153]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1893","summary":"This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":150508062,"end":150513789,"strand":1,"description":"extracellular matrix protein 1 [Source:HGNC Symbol;Acc:HGNC:3153]"}, {"versioned_ensembl_gene_id":"ENSG00000119318.12","gene_symbol":"RAD23B","gene_name":"RAD23 homolog B, nucleotide excision repair protein [Source:HGNC Symbol;Acc:HGNC:9813]","synonyms":"P58,HR23B,HHR23B","biotype":"protein_coding","ncbi_id":"5887","summary":"The protein encoded by this gene is one of two human homologs of Saccharomyces cerevisiae Rad23, a protein involved in the nucleotide excision repair (NER). This protein was found to be a component of the protein complex that specifically complements the NER defect of xeroderma pigmentosum group C (XP-c) cell extracts in vitro. This protein was also shown to interact with, and elevate the nucleotide excision activity of 3-methyladenine-DNA glycosylase (MPG), which suggested a role in DNA damage recognition in base excision repair. This protein contains an N-terminal ubiquitin-like domain, which was reported to interact with 26S proteasome, and thus this protein may be involved in the ubiquitin mediated proteolytic pathway in cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Sep 2011]","start":107283137,"end":107332194,"strand":1,"description":"RAD23 homolog B, nucleotide excision repair protein [Source:HGNC Symbol;Acc:HGNC:9813]"}, {"versioned_ensembl_gene_id":"ENSG00000259166.1","gene_symbol":"AL049836.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101447642,"end":101457117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253522.5","gene_symbol":"MIR3142HG","gene_name":"MIR3142 host gene [Source:HGNC Symbol;Acc:HGNC:51944]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107075116","summary":null,"start":160468268,"end":160487426,"strand":1,"description":"MIR3142 host gene [Source:HGNC Symbol;Acc:HGNC:51944]"}, {"versioned_ensembl_gene_id":"ENSG00000169136.10","gene_symbol":"ATF5","gene_name":"activating transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:790]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22809","summary":null,"start":49928702,"end":49933935,"strand":1,"description":"activating transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:790]"}, {"versioned_ensembl_gene_id":"ENSG00000196337.11","gene_symbol":"CGB7","gene_name":"chorionic gonadotropin beta subunit 7 [Source:HGNC Symbol;Acc:HGNC:16451]","synonyms":"CG-beta-a","biotype":"protein_coding","ncbi_id":"94027","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 7 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]","start":49054275,"end":49058860,"strand":-1,"description":"chorionic gonadotropin beta subunit 7 [Source:HGNC Symbol;Acc:HGNC:16451]"}, {"versioned_ensembl_gene_id":"ENSG00000213931.5","gene_symbol":"HBE1","gene_name":"hemoglobin subunit epsilon 1 [Source:HGNC Symbol;Acc:HGNC:4830]","synonyms":"HBE","biotype":"protein_coding","ncbi_id":"3046","summary":"The epsilon globin gene (HBE) is normally expressed in the embryonic yolk sac: two epsilon chains together with two zeta chains (an alpha-like globin) constitute the embryonic hemoglobin Hb Gower I; two epsilon chains together with two alpha chains form the embryonic Hb Gower II. Both of these embryonic hemoglobins are normally supplanted by fetal, and later, adult hemoglobin. The five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon - G-gamma - A-gamma - delta - beta-3' [provided by RefSeq, Jul 2008]","start":5268345,"end":5505617,"strand":-1,"description":"hemoglobin subunit epsilon 1 [Source:HGNC Symbol;Acc:HGNC:4830]"}, {"versioned_ensembl_gene_id":"ENSG00000170370.11","gene_symbol":"EMX2","gene_name":"empty spiracles homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3341]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2018","summary":"This gene encodes a homeobox-containing transcription factor that is the homolog to the 'empty spiracles' gene in Drosophila. Research on this gene in humans has focused on its expression in three tissues: dorsal telencephalon, olfactory neuroepithelium, and urogenetial system. It is expressed in the dorsal telencephalon during development in a low rostral-lateral to high caudal-medial gradient and is proposed to pattern the neocortex into defined functional areas. It is also expressed in embryonic and adult olfactory neuroepithelia where it complexes with eukaryotic translation initiation factor 4E (eIF4E) and possibly regulates mRNA transport or translation. In the developing urogenital system, it is expressed in epithelial tissues and is negatively regulated by HOXA10. Alternative splicing results in multiple transcript variants encoding distinct proteins.[provided by RefSeq, Sep 2009]","start":117542444,"end":117549546,"strand":1,"description":"empty spiracles homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3341]"}, {"versioned_ensembl_gene_id":"ENSG00000183098.10","gene_symbol":"GPC6","gene_name":"glypican 6 [Source:HGNC Symbol;Acc:HGNC:4454]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10082","summary":"The glypicans comprise a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans, and they have been implicated in the control of cell growth and cell division. The glypican encoded by this gene is a putative cell surface coreceptor for growth factors, extracellular matrix proteins, proteases and anti-proteases. Mutations in this gene are associated with omodysplasia 1. [provided by RefSeq, Nov 2016]","start":93226842,"end":94407401,"strand":1,"description":"glypican 6 [Source:HGNC Symbol;Acc:HGNC:4454]"}, {"versioned_ensembl_gene_id":"ENSG00000278917.1","gene_symbol":"AC006213.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":43891233,"end":43895411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119487.16","gene_symbol":"MAPKAP1","gene_name":"mitogen-activated protein kinase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18752]","synonyms":"SIN1,MIP1,MGC2745","biotype":"protein_coding","ncbi_id":"79109","summary":"This gene encodes a protein that is highly similar to the yeast SIN1 protein, a stress-activated protein kinase. Alternatively spliced transcript variants encoding distinct isoforms have been described. Alternate polyadenylation sites as well as alternate 3' UTRs have been identified for transcripts of this gene. [provided by RefSeq, Jul 2008]","start":125437393,"end":125707234,"strand":-1,"description":"mitogen-activated protein kinase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18752]"}, {"versioned_ensembl_gene_id":"ENSG00000117472.9","gene_symbol":"TSPAN1","gene_name":"tetraspanin 1 [Source:HGNC Symbol;Acc:HGNC:20657]","synonyms":"TSPAN-1,NET-1","biotype":"protein_coding","ncbi_id":"10103","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. [provided by RefSeq, Jul 2008]","start":46175073,"end":46185958,"strand":1,"description":"tetraspanin 1 [Source:HGNC Symbol;Acc:HGNC:20657]"}, {"versioned_ensembl_gene_id":"ENSG00000240344.8","gene_symbol":"PPIL3","gene_name":"peptidylprolyl isomerase like 3 [Source:HGNC Symbol;Acc:HGNC:9262]","synonyms":"CyPJ","biotype":"protein_coding","ncbi_id":"53938","summary":"This gene encodes a member of the cyclophilin family. Cyclophilins catalyze the cis-trans isomerization of peptidylprolyl imide bonds in oligopeptides. They have been proposed to act either as catalysts or as molecular chaperones in protein-folding events. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2008]","start":200870907,"end":200889303,"strand":-1,"description":"peptidylprolyl isomerase like 3 [Source:HGNC Symbol;Acc:HGNC:9262]"}, {"versioned_ensembl_gene_id":"ENSG00000013441.15","gene_symbol":"CLK1","gene_name":"CDC like kinase 1 [Source:HGNC Symbol;Acc:HGNC:2068]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1195","summary":"This gene encodes a member of the CDC2-like (or LAMMER) family of dual specificity protein kinases. In the nucleus, the encoded protein phosphorylates serine/arginine-rich proteins involved in pre-mRNA processing, releasing them into the nucleoplasm. The choice of splice sites during pre-mRNA processing may be regulated by the concentration of transacting factors, including serine/arginine rich proteins. Therefore, the encoded protein may play an indirect role in governing splice site selection. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":200853009,"end":200864744,"strand":-1,"description":"CDC like kinase 1 [Source:HGNC Symbol;Acc:HGNC:2068]"}, {"versioned_ensembl_gene_id":"ENSG00000227198.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480731","summary":null,"start":31658329,"end":31660721,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000085265.10","gene_symbol":"FCN1","gene_name":"ficolin 1 [Source:HGNC Symbol;Acc:HGNC:3623]","synonyms":"FCNM","biotype":"protein_coding","ncbi_id":"2219","summary":" The ficolin family of proteins are characterized by the presence of a leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like domain. The collagen-like and the fibrinogen-like domains are also found separately in other proteins such as complement protein C1q, C-type lectins known as collectins, and tenascins. However, all these proteins recognize different targets, and are functionally distinct. Ficolin 1 encoded by FCN1 is predominantly expressed in the peripheral blood leukocytes, and has been postulated to function as a plasma protein with elastin-binding activity. [provided by RefSeq, Jul 2008]","start":134905890,"end":134917963,"strand":-1,"description":"ficolin 1 [Source:HGNC Symbol;Acc:HGNC:3623]"}, {"versioned_ensembl_gene_id":"ENSG00000172354.9","gene_symbol":"GNB2","gene_name":"G protein subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:4398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2783","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. This gene contains a trinucleotide (CCG) repeat length polymorphism in its 5' UTR. [provided by RefSeq, Jul 2008]","start":100673531,"end":100679174,"strand":1,"description":"G protein subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:4398]"}, {"versioned_ensembl_gene_id":"ENSG00000269475.2","gene_symbol":"AC244102.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152682810,"end":152683842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160339.15","gene_symbol":"FCN2","gene_name":"ficolin 2 [Source:HGNC Symbol;Acc:HGNC:3624]","synonyms":"P35,ficolin-2,FCNL,EBP-37","biotype":"protein_coding","ncbi_id":"2220","summary":"The product of this gene belongs to the ficolin family of proteins. This family is characterized by the presence of a leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like domain. This gene is predominantly expressed in the liver, and has been shown to have carbohydrate binding and opsonic activities. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":134880812,"end":134887520,"strand":1,"description":"ficolin 2 [Source:HGNC Symbol;Acc:HGNC:3624]"}, {"versioned_ensembl_gene_id":"ENSG00000270072.1","gene_symbol":"AC090559.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47513605,"end":47514889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216642.1","gene_symbol":"AL136116.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143327275,"end":143327655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225752.1","gene_symbol":"AL023581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143094034,"end":143099645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170608.2","gene_symbol":"FOXA3","gene_name":"forkhead box A3 [Source:HGNC Symbol;Acc:HGNC:5023]","synonyms":"HNF3G","biotype":"protein_coding","ncbi_id":"3171","summary":"This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific transcripts such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. The crystal structure of a similar protein in rat has been resolved. [provided by RefSeq, Jul 2008]","start":45863989,"end":45873797,"strand":1,"description":"forkhead box A3 [Source:HGNC Symbol;Acc:HGNC:5023]"}, {"versioned_ensembl_gene_id":"ENSG00000125447.16","gene_symbol":"GGA3","gene_name":"golgi associated, gamma adaptin ear containing, ARF binding protein 3 [Source:HGNC Symbol;Acc:HGNC:17079]","synonyms":"KIAA0154","biotype":"protein_coding","ncbi_id":"23163","summary":"This gene encodes a member of the Golgi-localized, gamma adaptin ear-containing, ARF-binding (GGA) family. This family includes ubiquitous coat proteins that regulate the trafficking of proteins between the trans-Golgi network and the lysosome. These proteins share an amino-terminal VHS domain which mediates sorting of the mannose 6-phosphate receptors at the trans-Golgi network. They also contain a carboxy-terminal region with homology to the ear domain of gamma-adaptins. Multiple alternatively spliced transcript variants have been identified in this gene. [provided by RefSeq, Feb 2010]","start":75236599,"end":75262363,"strand":-1,"description":"golgi associated, gamma adaptin ear containing, ARF binding protein 3 [Source:HGNC Symbol;Acc:HGNC:17079]"}, {"versioned_ensembl_gene_id":"ENSG00000204655.11","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTNL11,BTN6","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29656981,"end":29672372,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000171346.15","gene_symbol":"KRT15","gene_name":"keratin 15 [Source:HGNC Symbol;Acc:HGNC:6421]","synonyms":"K1CO,K15,CK15","biotype":"protein_coding","ncbi_id":"3866","summary":"The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region on chromosome 17q21.2. [provided by RefSeq, Jul 2008]","start":41513743,"end":41522529,"strand":-1,"description":"keratin 15 [Source:HGNC Symbol;Acc:HGNC:6421]"}, {"versioned_ensembl_gene_id":"ENSG00000146416.17","gene_symbol":"AIG1","gene_name":"androgen induced 1 [Source:HGNC Symbol;Acc:HGNC:21607]","synonyms":"FLJ10485,dJ95L4.1,AIG-1","biotype":"protein_coding","ncbi_id":"51390","summary":null,"start":143060496,"end":143340304,"strand":1,"description":"androgen induced 1 [Source:HGNC Symbol;Acc:HGNC:21607]"}, {"versioned_ensembl_gene_id":"ENSG00000171401.14","gene_symbol":"KRT13","gene_name":"keratin 13 [Source:HGNC Symbol;Acc:HGNC:6415]","synonyms":"MGC3781,MGC161462,K13,CK13","biotype":"protein_coding","ncbi_id":"3860","summary":"The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008]","start":41500981,"end":41505705,"strand":-1,"description":"keratin 13 [Source:HGNC Symbol;Acc:HGNC:6415]"}, {"versioned_ensembl_gene_id":"ENSG00000240846.2","gene_symbol":"RPS15P9","gene_name":"ribosomal protein S15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36440]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401895","summary":null,"start":1307401,"end":1307719,"strand":-1,"description":"ribosomal protein S15 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36440]"}, {"versioned_ensembl_gene_id":"ENSG00000284686.1","gene_symbol":"AC119674.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56173433,"end":56524495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254684.1","gene_symbol":"AP002803.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85336075,"end":85336572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133678.13","gene_symbol":"TMEM254","gene_name":"transmembrane protein 254 [Source:HGNC Symbol;Acc:HGNC:25804]","synonyms":"FLJ13263,C10orf57,bA369J21.6","biotype":"protein_coding","ncbi_id":"80195","summary":null,"start":80078646,"end":80092557,"strand":1,"description":"transmembrane protein 254 [Source:HGNC Symbol;Acc:HGNC:25804]"}, {"versioned_ensembl_gene_id":"ENSG00000282432.1","gene_symbol":"AL356095.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80053428,"end":80053548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236776.1","gene_symbol":"RPL21P23","gene_name":"ribosomal protein L21 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36205]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270879","summary":null,"start":56538452,"end":56538911,"strand":1,"description":"ribosomal protein L21 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36205]"}, {"versioned_ensembl_gene_id":"ENSG00000213641.4","gene_symbol":"RPL7AP4","gene_name":"ribosomal protein L7a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652985","summary":null,"start":55543401,"end":55544169,"strand":1,"description":"ribosomal protein L7a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23554]"}, {"versioned_ensembl_gene_id":"ENSG00000248492.1","gene_symbol":"ZFAT-AS1","gene_name":"ZFAT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33992]","synonyms":"ZFATAS,ZFAT-AS,SAS-ZFAT,NCRNA00070","biotype":"antisense_RNA","ncbi_id":"594840","summary":"This gene encodes a small antisense RNA that may be involved in regulating the sense strand locus, zinc finger and AT hook domain containing. This RNA may play a role in B cell function. A single nucleotide polymorphism in the promoter of this gene is associated with an increased risk of autoimmune thyroid disease.[provided by RefSeq, Jan 2010]","start":134598071,"end":134600689,"strand":1,"description":"ZFAT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33992]"}, {"versioned_ensembl_gene_id":"ENSG00000086730.16","gene_symbol":"LAT2","gene_name":"linker for activation of T-cells family member 2 [Source:HGNC Symbol;Acc:HGNC:12749]","synonyms":"WSCR5,WBSCR5,WBSCR15,NTAL,LAB,HSPC046","biotype":"protein_coding","ncbi_id":"7462","summary":"This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]","start":74199652,"end":74229834,"strand":1,"description":"linker for activation of T-cells family member 2 [Source:HGNC Symbol;Acc:HGNC:12749]"}, {"versioned_ensembl_gene_id":"ENSG00000198435.3","gene_symbol":"NRARP","gene_name":"NOTCH regulated ankyrin repeat protein [Source:HGNC Symbol;Acc:HGNC:33843]","synonyms":"MGC61598","biotype":"protein_coding","ncbi_id":"441478","summary":null,"start":137300482,"end":137302251,"strand":-1,"description":"NOTCH regulated ankyrin repeat protein [Source:HGNC Symbol;Acc:HGNC:33843]"}, {"versioned_ensembl_gene_id":"ENSG00000260996.1","gene_symbol":"BX255925.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":137293868,"end":137295721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225655.5","gene_symbol":"BX255923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41073710,"end":41076392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136869.13","gene_symbol":"TLR4","gene_name":"toll like receptor 4 [Source:HGNC Symbol;Acc:HGNC:11850]","synonyms":"TLR-4,hToll,CD284,ARMD10","biotype":"protein_coding","ncbi_id":"7099","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. In silico studies have found a particularly strong binding of surface TLR4 with the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of Coronavirus disease-2019 (COVID-19). This receptor has also been implicated in signal transduction events induced by lipopolysaccharide (LPS) found in most gram-negative bacteria. Mutations in this gene have been associated with differences in LPS responsiveness, and with susceptibility to age-related macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2020]","start":117704332,"end":117716871,"strand":1,"description":"toll like receptor 4 [Source:HGNC Symbol;Acc:HGNC:11850]"}, {"versioned_ensembl_gene_id":"ENSG00000139626.15","gene_symbol":"ITGB7","gene_name":"integrin subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:6162]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3695","summary":"This gene encodes a protein that is a member of the integrin superfamily. Members of this family are adhesion receptors that function in signaling from the extracellular matrix to the cell. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. The encoded protein forms dimers with an alpha4 chain or an alphaE chain and plays a role in leukocyte adhesion. Dimerization with alpha4 forms a homing receptor for migration of lymphocytes to the intestinal mucosa and Peyer's patches. Dimerization with alphaE permits binding to the ligand epithelial cadherin, a calcium-dependent adhesion molecule. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Sep 2013]","start":53191318,"end":53207307,"strand":-1,"description":"integrin subunit beta 7 [Source:HGNC Symbol;Acc:HGNC:6162]"}, {"versioned_ensembl_gene_id":"ENSG00000163625.15","gene_symbol":"WDFY3","gene_name":"WD repeat and FYVE domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20751]","synonyms":"ALFY,ZFYVE25,KIAA0993","biotype":"protein_coding","ncbi_id":"23001","summary":"This gene encodes a phosphatidylinositol 3-phosphate-binding protein that functions as a master conductor for aggregate clearance by autophagy. This protein shuttles from the nuclear membrane to colocalize with aggregated proteins, where it complexes with other autophagic components to achieve macroautophagy-mediated clearance of these aggregated proteins. However, it is not necessary for starvation-induced macroautophagy. [provided by RefSeq, May 2010]","start":84669610,"end":84966391,"strand":-1,"description":"WD repeat and FYVE domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20751]"}, {"versioned_ensembl_gene_id":"ENSG00000233198.3","gene_symbol":"RNF224","gene_name":"ring finger protein 224 [Source:HGNC Symbol;Acc:HGNC:41912]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643596","summary":null,"start":137227271,"end":137229638,"strand":1,"description":"ring finger protein 224 [Source:HGNC Symbol;Acc:HGNC:41912]"}, {"versioned_ensembl_gene_id":"ENSG00000232286.1","gene_symbol":"AL121902.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52858338,"end":52862855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225433.3","gene_symbol":"MTND1P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42061]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480744","summary":null,"start":11445418,"end":11445564,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42061]"}, {"versioned_ensembl_gene_id":"ENSG00000234859.5","gene_symbol":"AC003958.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41402416,"end":41425049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224710.3","gene_symbol":"FAM90A8P","gene_name":"family with sequence similarity 90 member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:32256]","synonyms":"FAM90A8","biotype":"unprocessed_pseudogene","ncbi_id":"441324","summary":"FAM90A8 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7738387,"end":7741396,"strand":1,"description":"family with sequence similarity 90 member A8, pseudogene [Source:HGNC Symbol;Acc:HGNC:32256]"}, {"versioned_ensembl_gene_id":"ENSG00000094796.4","gene_symbol":"KRT31","gene_name":"keratin 31 [Source:HGNC Symbol;Acc:HGNC:6448]","synonyms":"Ha-1,KRTHA1","biotype":"protein_coding","ncbi_id":"3881","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41393724,"end":41397592,"strand":-1,"description":"keratin 31 [Source:HGNC Symbol;Acc:HGNC:6448]"}, {"versioned_ensembl_gene_id":"ENSG00000282017.1","gene_symbol":"MTRNR2L6","gene_name":"MT-RNR2-like 6 [Source:HGNC Symbol;Acc:HGNC:37163]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463482","summary":null,"start":142706945,"end":142708391,"strand":1,"description":"MT-RNR2-like 6 [Source:HGNC Symbol;Acc:HGNC:37163]"}, {"versioned_ensembl_gene_id":"ENSG00000164754.14","gene_symbol":"RAD21","gene_name":"RAD21 cohesin complex component [Source:HGNC Symbol;Acc:HGNC:9811]","synonyms":"SCC1,KIAA0078,hHR21","biotype":"protein_coding","ncbi_id":"5885","summary":"The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad21, a gene involved in the repair of DNA double-strand breaks, as well as in chromatid cohesion during mitosis. This protein is a nuclear phospho-protein, which becomes hyperphosphorylated in cell cycle M phase. The highly regulated association of this protein with mitotic chromatin specifically at the centromere region suggests its role in sister chromatid cohesion in mitotic cells. [provided by RefSeq, Jul 2008]","start":116845935,"end":116874866,"strand":-1,"description":"RAD21 cohesin complex component [Source:HGNC Symbol;Acc:HGNC:9811]"}, {"versioned_ensembl_gene_id":"ENSG00000257787.1","gene_symbol":"AC112481.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90809276,"end":90810680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226622.5","gene_symbol":"AC092155.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62590255,"end":62662654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259356.1","gene_symbol":"AC022710.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100126106,"end":100129743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258183.5","gene_symbol":"LINC02392","gene_name":"long intergenic non-protein coding RNA 2392 [Source:HGNC Symbol;Acc:HGNC:53319]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369893","summary":null,"start":90280894,"end":90300340,"strand":1,"description":"long intergenic non-protein coding RNA 2392 [Source:HGNC Symbol;Acc:HGNC:53319]"}, {"versioned_ensembl_gene_id":"ENSG00000258216.5","gene_symbol":"AC084200.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89882665,"end":89989289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271048.1","gene_symbol":"AC087045.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134673131,"end":134673512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214886.4","gene_symbol":"FAM177A1P1","gene_name":"family with sequence similarity 177 member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34441]","synonyms":"FAM177A2","biotype":"processed_pseudogene","ncbi_id":"728710","summary":null,"start":98955982,"end":98956767,"strand":1,"description":"family with sequence similarity 177 member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34441]"}, {"versioned_ensembl_gene_id":"ENSG00000072506.12","gene_symbol":"HSD17B10","gene_name":"hydroxysteroid 17-beta dehydrogenase 10 [Source:HGNC Symbol;Acc:HGNC:4800]","synonyms":"MRXS10,MRPP2,MHBD,HADH2,ERAB,CAMR,ABAD,17b-HSD10,SDR5C1","biotype":"protein_coding","ncbi_id":"3028","summary":"This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids and steroids, and is a subunit of mitochondrial ribonuclease P, which is involved in tRNA maturation. The protein has been implicated in the development of Alzheimer disease, and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Aug 2014]","start":53431258,"end":53434373,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 10 [Source:HGNC Symbol;Acc:HGNC:4800]"}, {"versioned_ensembl_gene_id":"ENSG00000172732.11","gene_symbol":"MUS81","gene_name":"MUS81 structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:29814]","synonyms":"SLX3,FLJ44872","biotype":"protein_coding","ncbi_id":"80198","summary":"This gene encodes a structure-specific endonuclease which belongs to the XPF/MUS81 endonuclease family and plays a critical role in the resolution of recombination intermediates during DNA repair after inter-strand cross-links, replication fork collapse, and DNA double-strand breaks. The encoded protein associates with one of two closely related essential meiotic endonuclease proteins (EME1 or EME2) to form a complex that processes DNA secondary structures. It contains an N-terminal DEAH helicase domain, an excision repair cross complementation group 4 (ERCC4) endonuclease domain, and two tandem C-terminal helix-hairpin-helix domains. Mice with a homozygous knockout of the orthologous gene have significant meiotic defects including the failure to repair a subset of DNA double strand breaks. [provided by RefSeq, Jun 2017]","start":65857126,"end":65867653,"strand":1,"description":"MUS81 structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:29814]"}, {"versioned_ensembl_gene_id":"ENSG00000225918.1","gene_symbol":"RPL7P59","gene_name":"ribosomal protein L7 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:49215]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643308","summary":null,"start":145039999,"end":145040941,"strand":-1,"description":"ribosomal protein L7 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:49215]"}, {"versioned_ensembl_gene_id":"ENSG00000264577.1","gene_symbol":"AC010761.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28721487,"end":28722877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161640.15","gene_symbol":"SIGLEC11","gene_name":"sialic acid binding Ig like lectin 11 [Source:HGNC Symbol;Acc:HGNC:15622]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114132","summary":"This gene encodes a member of the sialic acid-binding immunoglobulin-like lectin family. These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain. This family member mediates anti-inflammatory and immunosuppressive signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":49948985,"end":49961172,"strand":-1,"description":"sialic acid binding Ig like lectin 11 [Source:HGNC Symbol;Acc:HGNC:15622]"}, {"versioned_ensembl_gene_id":"ENSG00000250371.1","gene_symbol":"AC007370.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12859101,"end":12864961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268006.1","gene_symbol":"PTOV1-AS1","gene_name":"PTOV1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44174]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506033","summary":null,"start":49838639,"end":49851676,"strand":-1,"description":"PTOV1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44174]"}, {"versioned_ensembl_gene_id":"ENSG00000214035.3","gene_symbol":"AC073310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145009961,"end":145010993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232987.1","gene_symbol":"LINC01219","gene_name":"long intergenic non-protein coding RNA 1219 [Source:HGNC Symbol;Acc:HGNC:49653]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355220","summary":null,"start":1991096,"end":1993469,"strand":1,"description":"long intergenic non-protein coding RNA 1219 [Source:HGNC Symbol;Acc:HGNC:49653]"}, {"versioned_ensembl_gene_id":"ENSG00000196860.7","gene_symbol":"TOMM20L","gene_name":"translocase of outer mitochondrial membrane 20 like [Source:HGNC Symbol;Acc:HGNC:33752]","synonyms":"UNQ9438","biotype":"protein_coding","ncbi_id":"387990","summary":null,"start":58395916,"end":58408701,"strand":1,"description":"translocase of outer mitochondrial membrane 20 like [Source:HGNC Symbol;Acc:HGNC:33752]"}, {"versioned_ensembl_gene_id":"ENSG00000235666.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SUMO2P,SMT3Bp,dJ271M21,SMT3H2P","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29636562,"end":29636845,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000256298.1","gene_symbol":"AC135388.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130047132,"end":130048376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282483.1","gene_symbol":"AC229888.8","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142643462,"end":142644194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166828.2","gene_symbol":"SCNN1G","gene_name":"sodium channel epithelial 1 gamma subunit [Source:HGNC Symbol;Acc:HGNC:10602]","synonyms":"SCNEG,ENaCgamma","biotype":"protein_coding","ncbi_id":"6340","summary":"Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the gamma subunit, and mutations in this gene have been associated with Liddle syndrome. [provided by RefSeq, Apr 2009]","start":23182715,"end":23216883,"strand":1,"description":"sodium channel epithelial 1 gamma subunit [Source:HGNC Symbol;Acc:HGNC:10602]"}, {"versioned_ensembl_gene_id":"ENSG00000186889.9","gene_symbol":"TMEM17","gene_name":"transmembrane protein 17 [Source:HGNC Symbol;Acc:HGNC:26623]","synonyms":"FLJ34583","biotype":"protein_coding","ncbi_id":"200728","summary":null,"start":62500221,"end":62511894,"strand":-1,"description":"transmembrane protein 17 [Source:HGNC Symbol;Acc:HGNC:26623]"}, {"versioned_ensembl_gene_id":"ENSG00000280090.2","gene_symbol":"OR8B4","gene_name":"olfactory receptor family 8 subfamily B member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8473]","synonyms":"OR8B4P","biotype":"protein_coding","ncbi_id":"283162","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":124423904,"end":124424893,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8473]"}, {"versioned_ensembl_gene_id":"ENSG00000110700.6","gene_symbol":"RPS13","gene_name":"ribosomal protein S13 [Source:HGNC Symbol;Acc:HGNC:10386]","synonyms":"S13","biotype":"protein_coding","ncbi_id":"6207","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S15P family of ribosomal proteins. It is located in the cytoplasm. The protein has been shown to bind to the 5.8S rRNA in rat. The gene product of the E. coli ortholog (ribosomal protein S15) functions at early steps in ribosome assembly. This gene is co-transcribed with two U14 small nucleolar RNA genes, which are located in its third and fifth introns. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":17074389,"end":17077787,"strand":-1,"description":"ribosomal protein S13 [Source:HGNC Symbol;Acc:HGNC:10386]"}, {"versioned_ensembl_gene_id":"ENSG00000255528.1","gene_symbol":"AP003123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109002465,"end":109037967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279594.1","gene_symbol":"AL049780.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75011269,"end":75012851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236193.3","gene_symbol":"LINC01953","gene_name":"long intergenic non-protein coding RNA 1953 [Source:HGNC Symbol;Acc:HGNC:52776]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373863","summary":null,"start":213155806,"end":213167712,"strand":-1,"description":"long intergenic non-protein coding RNA 1953 [Source:HGNC Symbol;Acc:HGNC:52776]"}, {"versioned_ensembl_gene_id":"ENSG00000228707.1","gene_symbol":"AL691426.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116012361,"end":116012965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233455.2","gene_symbol":"AL035414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210303684,"end":210304540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220557.1","gene_symbol":"HMGB1P13","gene_name":"high mobility group box 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:13318]","synonyms":"HMGB1L13","biotype":"processed_pseudogene","ncbi_id":"100129706","summary":null,"start":132868218,"end":132868859,"strand":-1,"description":"high mobility group box 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:13318]"}, {"versioned_ensembl_gene_id":"ENSG00000282354.1","gene_symbol":"AC229888.5","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142605549,"end":142606054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233003.4","gene_symbol":"CICP26","gene_name":"capicua transcriptional repressor pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:48834]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"648262","summary":null,"start":227975390,"end":227978193,"strand":-1,"description":"capicua transcriptional repressor pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:48834]"}, {"versioned_ensembl_gene_id":"ENSG00000213416.3","gene_symbol":"KRTAP4-12","gene_name":"keratin associated protein 4-12 [Source:HGNC Symbol;Acc:HGNC:16776]","synonyms":"KAP4.12","biotype":"protein_coding","ncbi_id":"83755","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41123091,"end":41124167,"strand":-1,"description":"keratin associated protein 4-12 [Source:HGNC Symbol;Acc:HGNC:16776]"}, {"versioned_ensembl_gene_id":"ENSG00000229419.1","gene_symbol":"RALGAPA1P1","gene_name":"Ral GTPase activating protein catalytic alpha subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23203]","synonyms":"RALGAPA1P,GARNL2P,GARNL2,DKFZp566D133","biotype":"processed_pseudogene","ncbi_id":"26134","summary":null,"start":105520128,"end":105526359,"strand":1,"description":"Ral GTPase activating protein catalytic alpha subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23203]"}, {"versioned_ensembl_gene_id":"ENSG00000269102.1","gene_symbol":"AC010320.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52284780,"end":52297920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253772.1","gene_symbol":"AC112191.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160247517,"end":160248217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237230.1","gene_symbol":"KRTAP2-5P","gene_name":"keratin associated protein 2-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18920]","synonyms":"KRTAP2P1,KAP2A","biotype":"unprocessed_pseudogene","ncbi_id":"85343","summary":null,"start":41071946,"end":41072341,"strand":1,"description":"keratin associated protein 2-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18920]"}, {"versioned_ensembl_gene_id":"ENSG00000087088.19","gene_symbol":"BAX","gene_name":"BCL2 associated X, apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:959]","synonyms":"BCL2L4","biotype":"protein_coding","ncbi_id":"581","summary":"The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. This protein forms a heterodimer with BCL2, and functions as an apoptotic activator. The association and the ratio of BAX to BCL2 also determines survival or death of a cell following an apoptotic stimulus. This protein is reported to interact with, and increase the opening of, the mitochondrial voltage-dependent anion channel (VDAC), which leads to the loss in membrane potential and the release of cytochrome c. The expression of this gene is regulated by the tumor suppressor P53 and has been shown to be involved in P53-mediated apoptosis. Multiple alternatively spliced transcript variants, which encode different isoforms, have been reported for this gene. [provided by RefSeq, Dec 2019]","start":48954815,"end":48961798,"strand":1,"description":"BCL2 associated X, apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:959]"}, {"versioned_ensembl_gene_id":"ENSG00000277562.1","gene_symbol":"AC010320.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52241765,"end":52242440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213417.3","gene_symbol":"KRTAP2-4","gene_name":"keratin associated protein 2-4 [Source:HGNC Symbol;Acc:HGNC:18891]","synonyms":"KAP2.4","biotype":"protein_coding","ncbi_id":"85294","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41065116,"end":41065879,"strand":-1,"description":"keratin associated protein 2-4 [Source:HGNC Symbol;Acc:HGNC:18891]"}, {"versioned_ensembl_gene_id":"ENSG00000228136.1","gene_symbol":"AL773545.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40130921,"end":40153147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236461.1","gene_symbol":"AL162425.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115119539,"end":115138409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235420.7","gene_symbol":"AC009269.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":70796597,"end":70802688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156885.5","gene_symbol":"COX6A2","gene_name":"cytochrome c oxidase subunit 6A2 [Source:HGNC Symbol;Acc:HGNC:2279]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1339","summary":"Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 2 (heart/muscle isoform) of subunit VIa, and polypeptide 2 is present only in striated muscles. Polypeptide 1 (liver isoform) of subunit VIa is encoded by a different gene, and is found in all non-muscle tissues. These two polypeptides share 66% amino acid sequence identity. [provided by RefSeq, Jul 2008]","start":31427731,"end":31428428,"strand":-1,"description":"cytochrome c oxidase subunit 6A2 [Source:HGNC Symbol;Acc:HGNC:2279]"}, {"versioned_ensembl_gene_id":"ENSG00000186407.6","gene_symbol":"CD300E","gene_name":"CD300e molecule [Source:HGNC Symbol;Acc:HGNC:28874]","synonyms":"IREM2,CLM2,CD300LE","biotype":"protein_coding","ncbi_id":"342510","summary":"This gene encodes a member of the CD300 glycoprotein family of cell surface proteins expressed on myeloid cells. The protein interacts with the TYRO protein tyrosine kinase-binding protein and is thought to act as an activating receptor. [provided by RefSeq, Nov 2012]","start":74609887,"end":74623738,"strand":-1,"description":"CD300e molecule [Source:HGNC Symbol;Acc:HGNC:28874]"}, {"versioned_ensembl_gene_id":"ENSG00000212725.3","gene_symbol":"KRTAP2-1","gene_name":"keratin associated protein 2-1 [Source:HGNC Symbol;Acc:HGNC:16775]","synonyms":"KAP2.1A","biotype":"protein_coding","ncbi_id":"81872","summary":null,"start":41046541,"end":41047316,"strand":-1,"description":"keratin associated protein 2-1 [Source:HGNC Symbol;Acc:HGNC:16775]"}, {"versioned_ensembl_gene_id":"ENSG00000250383.1","gene_symbol":"AC008871.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108818041,"end":108830790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261222.2","gene_symbol":"AC064805.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74599840,"end":74607229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185888.5","gene_symbol":"PRSS38","gene_name":"protease, serine 38 [Source:HGNC Symbol;Acc:HGNC:29625]","synonyms":"MPN2","biotype":"protein_coding","ncbi_id":"339501","summary":null,"start":227815693,"end":227846470,"strand":1,"description":"protease, serine 38 [Source:HGNC Symbol;Acc:HGNC:29625]"}, {"versioned_ensembl_gene_id":"ENSG00000251234.1","gene_symbol":"PSMA2P2","gene_name":"proteasome subunit alpha 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43833]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131775","summary":null,"start":93939364,"end":93942877,"strand":-1,"description":"proteasome subunit alpha 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43833]"}, {"versioned_ensembl_gene_id":"ENSG00000272523.1","gene_symbol":"LINC01023","gene_name":"long intergenic non-protein coding RNA 1023 [Source:HGNC Symbol;Acc:HGNC:49004]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652853","summary":null,"start":108727825,"end":108728260,"strand":-1,"description":"long intergenic non-protein coding RNA 1023 [Source:HGNC Symbol;Acc:HGNC:49004]"}, {"versioned_ensembl_gene_id":"ENSG00000167850.3","gene_symbol":"CD300C","gene_name":"CD300c molecule [Source:HGNC Symbol;Acc:HGNC:19320]","synonyms":"LIR,IGSF16,CMRF35A,CMRF35,CMRF-35A","biotype":"protein_coding","ncbi_id":"10871","summary":"The CMRF35 antigen, which was identified by reactivity with a monoclonal antibody, is present on monocytes, neutrophils, and some T and B lymphocytes (Jackson et al., 1992 [PubMed 1349532]).[supplied by OMIM, Mar 2008]","start":74541108,"end":74546143,"strand":-1,"description":"CD300c molecule [Source:HGNC Symbol;Acc:HGNC:19320]"}, {"versioned_ensembl_gene_id":"ENSG00000160179.18","gene_symbol":"ABCG1","gene_name":"ATP binding cassette subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:73]","synonyms":"ABC8","biotype":"protein_coding","ncbi_id":"9619","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. It is involved in macrophage cholesterol and phospholipids transport, and may regulate cellular lipid homeostasis in other cell types. Six alternative splice variants have been identified. [provided by RefSeq, Jul 2008]","start":42199689,"end":42297244,"strand":1,"description":"ATP binding cassette subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:73]"}, {"versioned_ensembl_gene_id":"ENSG00000248827.1","gene_symbol":"AC024587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107724961,"end":107727117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204887.4","gene_symbol":"KRTAP1-4","gene_name":"keratin associated protein 1-4 [Source:HGNC Symbol;Acc:HGNC:18904]","synonyms":"KAP1.4","biotype":"protein_coding","ncbi_id":"728255","summary":"The main structural proteins of mammalian hair fiber are the hair keratins (see MIM 601077) and the keratin-associated proteins (KAPs), which form a rigid and resistant hair shaft through extensive disulfide bond crosslinking with the abundant cysteines of hair keratins (Shimomura et al., 2002 [PubMed 12228244]).[supplied by OMIM, Jan 2009]","start":41029697,"end":41030104,"strand":-1,"description":"keratin associated protein 1-4 [Source:HGNC Symbol;Acc:HGNC:18904]"}, {"versioned_ensembl_gene_id":"ENSG00000280242.1","gene_symbol":"AL450226.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2255719,"end":2256157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236457.1","gene_symbol":"AC090617.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2215482,"end":2216015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283197.1","gene_symbol":"AC103706.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133516184,"end":133516268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212899.2","gene_symbol":"KRTAP3-3","gene_name":"keratin associated protein 3-3 [Source:HGNC Symbol;Acc:HGNC:18890]","synonyms":"KAP3.3","biotype":"protein_coding","ncbi_id":"85293","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":40993430,"end":40994133,"strand":-1,"description":"keratin associated protein 3-3 [Source:HGNC Symbol;Acc:HGNC:18890]"}, {"versioned_ensembl_gene_id":"ENSG00000138614.14","gene_symbol":"INTS14","gene_name":"integrator complex subunit 14 [Source:HGNC Symbol;Acc:HGNC:25372]","synonyms":"VWA9,DKFZP564O1664,C15orf44","biotype":"protein_coding","ncbi_id":"81556","summary":null,"start":65578753,"end":65611289,"strand":-1,"description":"integrator complex subunit 14 [Source:HGNC Symbol;Acc:HGNC:25372]"}, {"versioned_ensembl_gene_id":"ENSG00000206283.10","gene_symbol":"PFDN6","gene_name":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]","synonyms":"HKE2,H2-KE2,PFD6,KE-2","biotype":"protein_coding","ncbi_id":"10471","summary":"PFDN6 is a subunit of the heteromeric prefoldin complex that chaperones nascent actin (see MIM 102560) and alpha- and beta-tubulin (see MIM 602529 and MIM 191130, respectively) chains pending their transfer to the cytosolic chaperonin containing TCP1 (MIM 186980) (CCT) complex (Hansen et al., 1999 [PubMed 10209023]).[supplied by OMIM, Jul 2010]","start":33218133,"end":33227229,"strand":1,"description":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]"}, {"versioned_ensembl_gene_id":"ENSG00000169174.10","gene_symbol":"PCSK9","gene_name":"proprotein convertase subtilisin/kexin type 9 [Source:HGNC Symbol;Acc:HGNC:20001]","synonyms":"FH3,NARC-1,HCHOLA3","biotype":"protein_coding","ncbi_id":"255738","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an autocatalytic processing event with its prosegment in the ER and is constitutively secreted as an inactive protease into the extracellular matrix and trans-Golgi network. It is expressed in liver, intestine and kidney tissues and escorts specific receptors for lysosomal degradation. It plays a role in cholesterol and fatty acid metabolism. Mutations in this gene have been associated with autosomal dominant familial hypercholesterolemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":55039548,"end":55064852,"strand":1,"description":"proprotein convertase subtilisin/kexin type 9 [Source:HGNC Symbol;Acc:HGNC:20001]"}, {"versioned_ensembl_gene_id":"ENSG00000254737.2","gene_symbol":"OR10G4","gene_name":"olfactory receptor family 10 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:14809]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390264","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124012997,"end":124018732,"strand":1,"description":"olfactory receptor family 10 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:14809]"}, {"versioned_ensembl_gene_id":"ENSG00000283178.1","gene_symbol":"BX119927.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71869763,"end":71873295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181518.4","gene_symbol":"OR8D4","gene_name":"olfactory receptor family 8 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:14840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338662","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123902167,"end":123909229,"strand":1,"description":"olfactory receptor family 8 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:14840]"}, {"versioned_ensembl_gene_id":"ENSG00000141579.6","gene_symbol":"ZNF750","gene_name":"zinc finger protein 750 [Source:HGNC Symbol;Acc:HGNC:25843]","synonyms":"Zfp750,FLJ13841","biotype":"protein_coding","ncbi_id":"79755","summary":"This gene encodes a protein with a nuclear localization site and a C2H2 zinc finger domain. Mutations in this gene have been associated with seborrhea-like dermatitis with psoriasiform elements. [provided by RefSeq, Jul 2008]","start":82829435,"end":82840578,"strand":-1,"description":"zinc finger protein 750 [Source:HGNC Symbol;Acc:HGNC:25843]"}, {"versioned_ensembl_gene_id":"ENSG00000260027.4","gene_symbol":"HOXB7","gene_name":"homeobox B7 [Source:HGNC Symbol;Acc:HGNC:5118]","synonyms":"HOX2C,HOX2","biotype":"protein_coding","ncbi_id":"3217","summary":"This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded nuclear protein functions as a sequence-specific transcription factor that is involved in cell proliferation and differentiation. Increased expression of this gene is associated with some cases of melanoma and ovarian carcinoma. [provided by RefSeq, Jul 2008]","start":48607227,"end":48633572,"strand":-1,"description":"homeobox B7 [Source:HGNC Symbol;Acc:HGNC:5118]"}, {"versioned_ensembl_gene_id":"ENSG00000228524.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"CDA12,HLA-59,D6S203,HLA-CDA12","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":29998699,"end":30002072,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000138386.16","gene_symbol":"NAB1","gene_name":"NGFI-A binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4664","summary":null,"start":190646746,"end":190692766,"strand":1,"description":"NGFI-A binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7626]"}, {"versioned_ensembl_gene_id":"ENSG00000277041.1","gene_symbol":"AC106788.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22537478,"end":22537584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172538.6","gene_symbol":"FAM170B","gene_name":"family with sequence similarity 170 member B [Source:HGNC Symbol;Acc:HGNC:19736]","synonyms":"Em:AC084727.4,C10orf73","biotype":"protein_coding","ncbi_id":"170370","summary":null,"start":49131154,"end":49134008,"strand":-1,"description":"family with sequence similarity 170 member B [Source:HGNC Symbol;Acc:HGNC:19736]"}, {"versioned_ensembl_gene_id":"ENSG00000184838.14","gene_symbol":"PRR16","gene_name":"proline rich 16 [Source:HGNC Symbol;Acc:HGNC:29654]","synonyms":"DSC54","biotype":"protein_coding","ncbi_id":"51334","summary":null,"start":120464278,"end":120687332,"strand":1,"description":"proline rich 16 [Source:HGNC Symbol;Acc:HGNC:29654]"}, {"versioned_ensembl_gene_id":"ENSG00000163440.11","gene_symbol":"PDCL2","gene_name":"phosducin like 2 [Source:HGNC Symbol;Acc:HGNC:29524]","synonyms":"GCPHLP","biotype":"protein_coding","ncbi_id":"132954","summary":"This gene encodes a member of the phosducin-like protein family and is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin. Members of the phosducin-like protein family have been shown to bind to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008]","start":55556525,"end":55592212,"strand":-1,"description":"phosducin like 2 [Source:HGNC Symbol;Acc:HGNC:29524]"}, {"versioned_ensembl_gene_id":"ENSG00000227137.8","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29356146,"end":29432443,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000271602.1","gene_symbol":"KRT8P49","gene_name":"keratin 8 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643447","summary":null,"start":4722740,"end":4724171,"strand":-1,"description":"keratin 8 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:48345]"}, {"versioned_ensembl_gene_id":"ENSG00000250294.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29417758,"end":29418704,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000237520.1","gene_symbol":"AL391832.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234957231,"end":234959989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279459.1","gene_symbol":"AP001271.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70603304,"end":70604859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106683.14","gene_symbol":"LIMK1","gene_name":"LIM domain kinase 1 [Source:HGNC Symbol;Acc:HGNC:6613]","synonyms":"LIMK","biotype":"protein_coding","ncbi_id":"3984","summary":"There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cognition of Williams syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Feb 2011]","start":74082933,"end":74122525,"strand":1,"description":"LIM domain kinase 1 [Source:HGNC Symbol;Acc:HGNC:6613]"}, {"versioned_ensembl_gene_id":"ENSG00000237148.1","gene_symbol":"HIGD1AP2","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874450","summary":null,"start":81272891,"end":81273170,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42642]"}, {"versioned_ensembl_gene_id":"ENSG00000167346.7","gene_symbol":"MMP26","gene_name":"matrix metallopeptidase 26 [Source:HGNC Symbol;Acc:HGNC:14249]","synonyms":"MGC126592,MGC126590,endometase","biotype":"protein_coding","ncbi_id":"56547","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme may degrade collagen type IV, fibronectin, fibrinogen, and beta-casein, and activate matrix metalloproteinase-9 by cleavage. The protein differs from most MMP family members in that it lacks a conserved C-terminal protein domain. The encoded protein may promote cell invasion in multiple human cancers. [provided by RefSeq, May 2016]","start":4704927,"end":4992429,"strand":1,"description":"matrix metallopeptidase 26 [Source:HGNC Symbol;Acc:HGNC:14249]"}, {"versioned_ensembl_gene_id":"ENSG00000105889.14","gene_symbol":"STEAP1B","gene_name":"STEAP family member 1B [Source:HGNC Symbol;Acc:HGNC:41907]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256227","summary":null,"start":22419444,"end":22632925,"strand":-1,"description":"STEAP family member 1B [Source:HGNC Symbol;Acc:HGNC:41907]"}, {"versioned_ensembl_gene_id":"ENSG00000230874.1","gene_symbol":"BX248084.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29230102,"end":29231032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230752.1","gene_symbol":"BX005432.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29263569,"end":29264945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239389.7","gene_symbol":"PCDHA13","gene_name":"protocadherin alpha 13 [Source:HGNC Symbol;Acc:HGNC:8667]","synonyms":"CRNR5,CNRS5,CNRN5,CNR5,PCDH-ALPHA13","biotype":"protein_coding","ncbi_id":"56136","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140882208,"end":141012344,"strand":1,"description":"protocadherin alpha 13 [Source:HGNC Symbol;Acc:HGNC:8667]"}, {"versioned_ensembl_gene_id":"ENSG00000205677.4","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"dJ570F3.6,APT,LYPLA2L","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33535893,"end":33536588,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000234277.2","gene_symbol":"LINC01641","gene_name":"long intergenic non-protein coding RNA 1641 [Source:HGNC Symbol;Acc:HGNC:52428]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985463","summary":null,"start":227393591,"end":227431035,"strand":1,"description":"long intergenic non-protein coding RNA 1641 [Source:HGNC Symbol;Acc:HGNC:52428]"}, {"versioned_ensembl_gene_id":"ENSG00000267203.1","gene_symbol":"AC115085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69318733,"end":69318961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129083.12","gene_symbol":"COPB1","gene_name":"coatomer protein complex subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:2231]","synonyms":"COPB","biotype":"protein_coding","ncbi_id":"1315","summary":"This gene encodes a protein subunit of the coatomer complex associated with non-clathrin coated vesicles. The coatomer complex, also known as the coat protein complex 1, forms in the cytoplasm and is recruited to the Golgi by activated guanosine triphosphatases. Once at the Golgi membrane, the coatomer complex may assist in the movement of protein and lipid components back to the endoplasmic reticulum. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009]","start":14443440,"end":14500027,"strand":-1,"description":"coatomer protein complex subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:2231]"}, {"versioned_ensembl_gene_id":"ENSG00000138592.13","gene_symbol":"USP8","gene_name":"ubiquitin specific peptidase 8 [Source:HGNC Symbol;Acc:HGNC:12631]","synonyms":"UBPY,SPG59,KIAA0055,HumORF8","biotype":"protein_coding","ncbi_id":"9101","summary":"This gene encodes a protein that belongs to the ubiquitin-specific processing protease family of proteins. The encoded protein is thought to regulate the morphology of the endosome by ubiquitination of proteins on this organelle and is involved in cargo sorting and membrane trafficking at the early endosome stage. This protein is required for the cell to enter the S phase of the cell cycle and also functions as a positive regulator in the Hedgehog signaling pathway in development. Pseudogenes of this gene are present on chromosomes 2 and 6. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":50424380,"end":50514419,"strand":1,"description":"ubiquitin specific peptidase 8 [Source:HGNC Symbol;Acc:HGNC:12631]"}, {"versioned_ensembl_gene_id":"ENSG00000188910.7","gene_symbol":"GJB3","gene_name":"gap junction protein beta 3 [Source:HGNC Symbol;Acc:HGNC:4285]","synonyms":"EKV,DFNA2,CX31","biotype":"protein_coding","ncbi_id":"2707","summary":"This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":34781189,"end":34786369,"strand":1,"description":"gap junction protein beta 3 [Source:HGNC Symbol;Acc:HGNC:4285]"}, {"versioned_ensembl_gene_id":"ENSG00000283517.1","gene_symbol":"AC005144.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71829870,"end":71871750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260785.1","gene_symbol":"CASC17","gene_name":"cancer susceptibility 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43911]","synonyms":"LINC00600","biotype":"lincRNA","ncbi_id":"101928165","summary":null,"start":71097775,"end":71202177,"strand":-1,"description":"cancer susceptibility 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43911]"}, {"versioned_ensembl_gene_id":"ENSG00000282405.1","gene_symbol":"AC019257.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1934747,"end":1938216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282101.1","gene_symbol":"AC019257.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1847451,"end":1847916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115339.13","gene_symbol":"GALNT3","gene_name":"polypeptide N-acetylgalactosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:4125]","synonyms":"HHS,HFTC,GalNAc-T3","biotype":"protein_coding","ncbi_id":"2591","summary":"This gene encodes UDP-GalNAc transferase 3, a member of the GalNAc-transferases family. This family transfers an N-acetyl galactosamine to the hydroxyl group of a serine or threonine residue in the first step of O-linked oligosaccharide biosynthesis. Individual GalNAc-transferases have distinct activities and initiation of O-glycosylation is regulated by a repertoire of GalNAc-transferases. The protein encoded by this gene is highly homologous to other family members, however the enzymes have different substrate specificities. [provided by RefSeq, Jul 2008]","start":165747591,"end":165794682,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:4125]"}, {"versioned_ensembl_gene_id":"ENSG00000270248.1","gene_symbol":"AC011468.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52110318,"end":52110726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173366.11","gene_symbol":"AC097637.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52221081,"end":52231190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229817.1","gene_symbol":"AL133412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114845594,"end":114848585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116035.2","gene_symbol":"VAX2","gene_name":"ventral anterior homeobox 2 [Source:HGNC Symbol;Acc:HGNC:12661]","synonyms":"DRES93","biotype":"protein_coding","ncbi_id":"25806","summary":"This gene encodes a homeobox protein and is almost exclusively expressed in the ventral portion of the retina during development. In mouse studies, this gene was found to be required for the correct formation of the optic fissure and other aspects of retinal development. [provided by RefSeq, Sep 2008]","start":70900590,"end":70933446,"strand":1,"description":"ventral anterior homeobox 2 [Source:HGNC Symbol;Acc:HGNC:12661]"}, {"versioned_ensembl_gene_id":"ENSG00000181634.7","gene_symbol":"TNFSF15","gene_name":"TNF superfamily member 15 [Source:HGNC Symbol;Acc:HGNC:11931]","synonyms":"MGC129934,VEGI192A,VEGI,TL1A,TL1,MGC129935","biotype":"protein_coding","ncbi_id":"9966","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein is abundantly expressed in endothelial cells, but is not expressed in either B or T cells. The expression of this protein is inducible by TNF and IL-1 alpha. This cytokine is a ligand for receptor TNFRSF25 and decoy receptor TNFRSF21/DR6. It can activate NF-kappaB and MAP kinases, and acts as an autocrine factor to induce apoptosis in endothelial cells. This cytokine is also found to inhibit endothelial cell proliferation, and thus may function as an angiogenesis inhibitor. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":114784635,"end":114806126,"strand":-1,"description":"TNF superfamily member 15 [Source:HGNC Symbol;Acc:HGNC:11931]"}, {"versioned_ensembl_gene_id":"ENSG00000167780.11","gene_symbol":"SOAT2","gene_name":"sterol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:11178]","synonyms":"ACAT2","biotype":"protein_coding","ncbi_id":"8435","summary":"Summary:This gene is a member of a small family of acyl coenzyme A:cholesterol acyltransferases. The gene encodes a membrane-bound enzyme localized in the endoplasmic reticulum that produces intracellular cholesterol esters from long-chain fatty acyl CoA and cholesterol. The cholesterol esters are then stored as cytoplasmic lipid droplets inside the cell. The enzyme is implicated in cholesterol absorption in the intestine and in the assembly and secretion of apolipoprotein B-containing lipoproteins such as very low density lipoprotein (VLDL). Several alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2008]","start":53103518,"end":53124538,"strand":1,"description":"sterol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:11178]"}, {"versioned_ensembl_gene_id":"ENSG00000258119.1","gene_symbol":"AC087897.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38544177,"end":38589812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278276.1","gene_symbol":"AL110115.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31580890,"end":31581214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102780.16","gene_symbol":"DGKH","gene_name":"diacylglycerol kinase eta [Source:HGNC Symbol;Acc:HGNC:2854]","synonyms":"DGKeta","biotype":"protein_coding","ncbi_id":"160851","summary":"This gene encodes a member of the diacylglycerol kinase (DGK) enzyme family. Members of this family are involved in regulating intracellular concentrations of diacylglycerol and phosphatidic acid. Variation in this gene has been associated with bipolar disorder. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2014]","start":42040036,"end":42256578,"strand":1,"description":"diacylglycerol kinase eta [Source:HGNC Symbol;Acc:HGNC:2854]"}, {"versioned_ensembl_gene_id":"ENSG00000258717.1","gene_symbol":"AL132711.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100675930,"end":100679884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248757.2","gene_symbol":"LINC02115","gene_name":"long intergenic non-protein coding RNA 2115 [Source:HGNC Symbol;Acc:HGNC:52970]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467212","summary":null,"start":103528434,"end":103541985,"strand":-1,"description":"long intergenic non-protein coding RNA 2115 [Source:HGNC Symbol;Acc:HGNC:52970]"}, {"versioned_ensembl_gene_id":"ENSG00000230284.1","gene_symbol":"AL160275.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114695922,"end":114696315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219814.2","gene_symbol":"RPL23AP47","gene_name":"ribosomal protein L23a pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36576]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729277","summary":null,"start":170745518,"end":170745977,"strand":1,"description":"ribosomal protein L23a pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36576]"}, {"versioned_ensembl_gene_id":"ENSG00000255233.1","gene_symbol":"AP003969.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93240133,"end":93241168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266101.1","gene_symbol":"AC004408.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39173290,"end":39177503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116031.8","gene_symbol":"CD207","gene_name":"CD207 molecule [Source:HGNC Symbol;Acc:HGNC:17935]","synonyms":"Langerin,CLEC4K","biotype":"protein_coding","ncbi_id":"50489","summary":"The protein encoded by this gene is expressed only in Langerhans cells which are immature dendritic cells of the epidermis and mucosa. It is localized in the Birbeck granules, organelles present in the cytoplasm of Langerhans cells and consisting of superimposed and zippered membranes. It is a C-type lectin with mannose binding specificity, and it has been proposed that mannose binding by this protein leads to internalization of antigen into Birbeck granules and providing access to a nonclassical antigen-processing pathway. Mutations in this gene result in Birbeck granules deficiency or loss of sugar binding activity. [provided by RefSeq, Aug 2010]","start":70830214,"end":70835822,"strand":-1,"description":"CD207 molecule [Source:HGNC Symbol;Acc:HGNC:17935]"}, {"versioned_ensembl_gene_id":"ENSG00000142173.14","gene_symbol":"COL6A2","gene_name":"collagen type VI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2212]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1292","summary":"This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]","start":46098097,"end":46132849,"strand":1,"description":"collagen type VI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2212]"}, {"versioned_ensembl_gene_id":"ENSG00000275055.1","gene_symbol":"AC011468.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52049007,"end":52049754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278180.1","gene_symbol":"AL451054.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":227490691,"end":227492296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133169.5","gene_symbol":"BEX1","gene_name":"brain expressed X-linked 1 [Source:HGNC Symbol;Acc:HGNC:1036]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55859","summary":null,"start":103062651,"end":103064240,"strand":-1,"description":"brain expressed X-linked 1 [Source:HGNC Symbol;Acc:HGNC:1036]"}, {"versioned_ensembl_gene_id":"ENSG00000233701.3","gene_symbol":"PRR23C","gene_name":"proline rich 23C [Source:HGNC Symbol;Acc:HGNC:37173]","synonyms":"FLJ46210","biotype":"protein_coding","ncbi_id":"389152","summary":null,"start":139042102,"end":139044892,"strand":-1,"description":"proline rich 23C [Source:HGNC Symbol;Acc:HGNC:37173]"}, {"versioned_ensembl_gene_id":"ENSG00000232416.3","gene_symbol":"BPESC1","gene_name":"blepharophimosis, epicanthus inversus and ptosis, candidate 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13228]","synonyms":"NCRNA00187","biotype":"lincRNA","ncbi_id":"60467","summary":null,"start":139104185,"end":139125171,"strand":1,"description":"blepharophimosis, epicanthus inversus and ptosis, candidate 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13228]"}, {"versioned_ensembl_gene_id":"ENSG00000281473.1","gene_symbol":"PISRT1","gene_name":"polled intersex syndrome regulated transcript 1 (non-protein coding RNA) [Source:HGNC Symbol;Acc:HGNC:16671]","synonyms":"NCRNA00195","biotype":"lincRNA","ncbi_id":"140464","summary":null,"start":139232992,"end":139233522,"strand":1,"description":"polled intersex syndrome regulated transcript 1 (non-protein coding RNA) [Source:HGNC Symbol;Acc:HGNC:16671]"}, {"versioned_ensembl_gene_id":"ENSG00000237193.1","gene_symbol":"AL451054.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227482253,"end":227482454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182742.5","gene_symbol":"HOXB4","gene_name":"homeobox B4 [Source:HGNC Symbol;Acc:HGNC:5115]","synonyms":"HOX2F,HOX2","biotype":"protein_coding","ncbi_id":"3214","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Intracellular or ectopic expression of this protein expands hematopoietic stem and progenitor cells in vivo and in vitro, making it a potential candidate for therapeutic stem cell expansion. [provided by RefSeq, Jul 2008]","start":48575513,"end":48580111,"strand":-1,"description":"homeobox B4 [Source:HGNC Symbol;Acc:HGNC:5115]"}, {"versioned_ensembl_gene_id":"ENSG00000247596.8","gene_symbol":"TWF2","gene_name":"twinfilin actin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9621]","synonyms":"PTK9L,A6RP,A6r","biotype":"protein_coding","ncbi_id":"11344","summary":"The protein encoded by this gene was identified by its interaction with the catalytic domain of protein kinase C-zeta. The encoded protein contains an actin-binding site and an ATP-binding site. It is most closely related to twinfilin (PTK9), a conserved actin monomer-binding protein. [provided by RefSeq, Jul 2008]","start":52228610,"end":52239260,"strand":-1,"description":"twinfilin actin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9621]"}, {"versioned_ensembl_gene_id":"ENSG00000224834.1","gene_symbol":"BTF3P9","gene_name":"basic transcription factor 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38573]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503543","summary":null,"start":227434064,"end":227434346,"strand":1,"description":"basic transcription factor 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38573]"}, {"versioned_ensembl_gene_id":"ENSG00000059588.9","gene_symbol":"TARBP1","gene_name":"TAR (HIV-1) RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11568]","synonyms":"TRP-185,TRMT3,TRM3","biotype":"protein_coding","ncbi_id":"6894","summary":"HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expression by the transactivator Tat is dependent on an RNA regulatory element (TAR) located downstream of the transcription initiation site. This element forms a stable stem-loop structure and can be bound by either the protein encoded by this gene or by RNA polymerase II. This protein may act to disengage RNA polymerase II from TAR during transcriptional elongation. Alternatively spliced transcripts of this gene may exist, but their full-length natures have not been determined. [provided by RefSeq, Jul 2008]","start":234391313,"end":234479103,"strand":-1,"description":"TAR (HIV-1) RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11568]"}, {"versioned_ensembl_gene_id":"ENSG00000152672.7","gene_symbol":"CLEC4F","gene_name":"C-type lectin domain family 4 member F [Source:HGNC Symbol;Acc:HGNC:25357]","synonyms":"KCLR,FLJ39110,CLECSF13","biotype":"protein_coding","ncbi_id":"165530","summary":null,"start":70808643,"end":70820600,"strand":-1,"description":"C-type lectin domain family 4 member F [Source:HGNC Symbol;Acc:HGNC:25357]"}, {"versioned_ensembl_gene_id":"ENSG00000108511.9","gene_symbol":"HOXB6","gene_name":"homeobox B6 [Source:HGNC Symbol;Acc:HGNC:5117]","synonyms":"HOX2B,HOX2","biotype":"protein_coding","ncbi_id":"3216","summary":"This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development, including that of lung and skin, and has been localized to both the nucleus and cytoplasm. Altered expression of this gene or a change in the subcellular localization of its protein is associated with some cases of acute myeloid leukemia and colorectal cancer. [provided by RefSeq, Jul 2008]","start":48595751,"end":48604992,"strand":-1,"description":"homeobox B6 [Source:HGNC Symbol;Acc:HGNC:5117]"}, {"versioned_ensembl_gene_id":"ENSG00000274919.1","gene_symbol":"AL390240.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114774737,"end":114775120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270741.1","gene_symbol":"PRELID3BP8","gene_name":"PRELI domain containing 3B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480243","summary":null,"start":120658077,"end":120658371,"strand":-1,"description":"PRELI domain containing 3B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49070]"}, {"versioned_ensembl_gene_id":"ENSG00000112874.9","gene_symbol":"NUDT12","gene_name":"nudix hydrolase 12 [Source:HGNC Symbol;Acc:HGNC:18826]","synonyms":"DKFZP761I172","biotype":"protein_coding","ncbi_id":"83594","summary":"Nucleotides are involved in numerous biochemical reactions and pathways within the cell as substrates, cofactors, and effectors. Nudix hydrolases, such as NUDT12, regulate the concentrations of individual nucleotides and of nucleotide ratios in response to changing circumstances (Abdelraheim et al., 2003 [PubMed 12790796]).[supplied by OMIM, Mar 2008]","start":103548855,"end":103562793,"strand":-1,"description":"nudix hydrolase 12 [Source:HGNC Symbol;Acc:HGNC:18826]"}, {"versioned_ensembl_gene_id":"ENSG00000242757.1","gene_symbol":"AL606462.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227430526,"end":227430976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232864.1","gene_symbol":"NUCKS1P1","gene_name":"nuclear casein kinase and cyclin dependent kinase substrate 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51943]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130466","summary":null,"start":227410617,"end":227411319,"strand":-1,"description":"nuclear casein kinase and cyclin dependent kinase substrate 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51943]"}, {"versioned_ensembl_gene_id":"ENSG00000238258.1","gene_symbol":"AL121748.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33211277,"end":33213804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133424.20","gene_symbol":"LARGE1","gene_name":"LARGE xylosyl- and glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:6511]","synonyms":"LARGE,KIAA0609","biotype":"protein_coding","ncbi_id":"9215","summary":"This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018]","start":33162226,"end":33922841,"strand":-1,"description":"LARGE xylosyl- and glucuronyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:6511]"}, {"versioned_ensembl_gene_id":"ENSG00000233650.1","gene_symbol":"BX248413.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29027504,"end":29028431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257178.5","gene_symbol":"AC103702.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48579630,"end":48582259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270688.1","gene_symbol":"AL137849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86228815,"end":86228983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180776.15","gene_symbol":"ZDHHC20","gene_name":"zinc finger DHHC-type containing 20 [Source:HGNC Symbol;Acc:HGNC:20749]","synonyms":"FLJ25952,DHHC20","biotype":"protein_coding","ncbi_id":"253832","summary":null,"start":21372573,"end":21459370,"strand":-1,"description":"zinc finger DHHC-type containing 20 [Source:HGNC Symbol;Acc:HGNC:20749]"}, {"versioned_ensembl_gene_id":"ENSG00000234105.1","gene_symbol":"AC009468.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53514992,"end":53517116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271194.1","gene_symbol":"RNF138P2","gene_name":"ring finger protein 138 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419777","summary":null,"start":53316149,"end":53316740,"strand":1,"description":"ring finger protein 138 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50775]"}, {"versioned_ensembl_gene_id":"ENSG00000226926.7","gene_symbol":"PDZPH1P","gene_name":"PDZ and pleckstrin homology domains 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:51488]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"105379197","summary":null,"start":103430406,"end":103526618,"strand":-1,"description":"PDZ and pleckstrin homology domains 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:51488]"}, {"versioned_ensembl_gene_id":"ENSG00000189195.11","gene_symbol":"AC104836.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":92080305,"end":92184725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225952.1","gene_symbol":"AL512444.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22835713,"end":22836849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235076.2","gene_symbol":"GAPDHP52","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:38558]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421313","summary":null,"start":21358373,"end":21359314,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:38558]"}, {"versioned_ensembl_gene_id":"ENSG00000236953.1","gene_symbol":"ZDHHC20-IT1","gene_name":"ZDHHC20 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39900]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874367","summary":null,"start":21376977,"end":21377874,"strand":-1,"description":"ZDHHC20 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39900]"}, {"versioned_ensembl_gene_id":"ENSG00000069712.12","gene_symbol":"KIAA1107","gene_name":"KIAA1107 [Source:HGNC Symbol;Acc:HGNC:29192]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23285","summary":null,"start":92166985,"end":92184723,"strand":1,"description":"KIAA1107 [Source:HGNC Symbol;Acc:HGNC:29192]"}, {"versioned_ensembl_gene_id":"ENSG00000010361.13","gene_symbol":"FUZ","gene_name":"fuzzy planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:26219]","synonyms":"Fy,FLJ22688","biotype":"protein_coding","ncbi_id":"80199","summary":"This gene encodes a planar cell polarity protein that is involved in ciliogenesis and directional cell movement. Knockout studies in mice exhibit neural tube defects and defective cilia, and mutations in this gene are associated with neural tube defects in humans. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2012]","start":49806869,"end":49817376,"strand":-1,"description":"fuzzy planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:26219]"}, {"versioned_ensembl_gene_id":"ENSG00000102128.8","gene_symbol":"RAB40AL","gene_name":"RAB40A like [Source:HGNC Symbol;Acc:HGNC:25410]","synonyms":"RLGP,RAR2","biotype":"protein_coding","ncbi_id":"282808","summary":"This gene encodes a member of the Rab40 subfamily of Rab small GTP-binding proteins that contains a C-terminal suppressors of cytokine signaling box. Disruptions in this gene are associated with Duchenne muscular dystrophy. [provided by RefSeq, Apr 2010]","start":102937272,"end":102938300,"strand":1,"description":"RAB40A like [Source:HGNC Symbol;Acc:HGNC:25410]"}, {"versioned_ensembl_gene_id":"ENSG00000233101.10","gene_symbol":"HOXB-AS3","gene_name":"HOXB cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40283]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"404266","summary":null,"start":48549630,"end":48606414,"strand":1,"description":"HOXB cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40283]"}, {"versioned_ensembl_gene_id":"ENSG00000277229.1","gene_symbol":"AC084781.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58454327,"end":58454982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257241.1","gene_symbol":"AC078922.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69946543,"end":69947081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161040.16","gene_symbol":"FBXL13","gene_name":"F-box and leucine rich repeat protein 13 [Source:HGNC Symbol;Acc:HGNC:21658]","synonyms":"MGC21636,Fbl13,DRC6","biotype":"protein_coding","ncbi_id":"222235","summary":"Members of the F-box protein family, such as FBXL13, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":102813230,"end":103074843,"strand":-1,"description":"F-box and leucine rich repeat protein 13 [Source:HGNC Symbol;Acc:HGNC:21658]"}, {"versioned_ensembl_gene_id":"ENSG00000171863.12","gene_symbol":"RPS7","gene_name":"ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:10440]","synonyms":"S7","biotype":"protein_coding","ncbi_id":"6201","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S7E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":3575205,"end":3580919,"strand":1,"description":"ribosomal protein S7 [Source:HGNC Symbol;Acc:HGNC:10440]"}, {"versioned_ensembl_gene_id":"ENSG00000257815.5","gene_symbol":"LINC01481","gene_name":"long intergenic non-protein coding RNA 1481 [Source:NCBI gene;Acc:101928062]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928062","summary":null,"start":69904033,"end":70243360,"strand":-1,"description":"long intergenic non-protein coding RNA 1481 [Source:NCBI gene;Acc:101928062]"}, {"versioned_ensembl_gene_id":"ENSG00000284024.1","gene_symbol":"AC069544.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14838166,"end":14844727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160551.11","gene_symbol":"TAOK1","gene_name":"TAO kinase 1 [Source:HGNC Symbol;Acc:HGNC:29259]","synonyms":"TAO1,PSK2,MARKK,MAP3K16,KIAA1361,FLJ14314","biotype":"protein_coding","ncbi_id":"57551","summary":null,"start":29390464,"end":29551904,"strand":1,"description":"TAO kinase 1 [Source:HGNC Symbol;Acc:HGNC:29259]"}, {"versioned_ensembl_gene_id":"ENSG00000128606.12","gene_symbol":"LRRC17","gene_name":"leucine rich repeat containing 17 [Source:HGNC Symbol;Acc:HGNC:16895]","synonyms":"P37NB,H_RG318M05.3","biotype":"protein_coding","ncbi_id":"10234","summary":null,"start":102912991,"end":102944949,"strand":1,"description":"leucine rich repeat containing 17 [Source:HGNC Symbol;Acc:HGNC:16895]"}, {"versioned_ensembl_gene_id":"ENSG00000236226.1","gene_symbol":"AC073127.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103030104,"end":103031354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248419.2","gene_symbol":"AC110768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10478524,"end":10478923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257346.1","gene_symbol":"AC011603.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49090208,"end":49093312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229839.6","gene_symbol":"AC018462.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62069447,"end":62146881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185267.9","gene_symbol":"CDNF","gene_name":"cerebral dopamine neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:24913]","synonyms":"ARMETL1","biotype":"protein_coding","ncbi_id":"441549","summary":null,"start":14819250,"end":14838575,"strand":-1,"description":"cerebral dopamine neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:24913]"}, {"versioned_ensembl_gene_id":"ENSG00000236498.1","gene_symbol":"AC107081.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61868432,"end":61886082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282577.1","gene_symbol":"TRBV5-5","gene_name":"T-cell receptor beta variable 5-5 [Source:HGNC Symbol;Acc:HGNC:12222]","synonyms":"TRBV55,TCRBV5S5,TCRBV5S3A2T","biotype":"TR_V_gene","ncbi_id":"28610","summary":null,"start":142504264,"end":142504735,"strand":1,"description":"T-cell receptor beta variable 5-5 [Source:HGNC Symbol;Acc:HGNC:12222]"}, {"versioned_ensembl_gene_id":"ENSG00000120094.6","gene_symbol":"HOXB1","gene_name":"homeobox B1 [Source:HGNC Symbol;Acc:HGNC:5111]","synonyms":"HOX2I,HOX2","biotype":"protein_coding","ncbi_id":"3211","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXB genes located in a cluster on chromosome 17. [provided by RefSeq, Jul 2008]","start":48528526,"end":48530997,"strand":-1,"description":"homeobox B1 [Source:HGNC Symbol;Acc:HGNC:5111]"}, {"versioned_ensembl_gene_id":"ENSG00000277672.1","gene_symbol":"AC011603.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49075039,"end":49075802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264451.1","gene_symbol":"AC036222.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48460370,"end":48466040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163932.13","gene_symbol":"PRKCD","gene_name":"protein kinase C delta [Source:HGNC Symbol;Acc:HGNC:9399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5580","summary":"The protein encoded by this gene is a member of the protein kinase C family of serine- and threonine-specific protein kinases. The encoded protein is activated by diacylglycerol and is both a tumor suppressor and a positive regulator of cell cycle progression. Also, this protein can positively or negatively regulate apoptosis. Defects in this gene are a cause of autoimmune lymphoproliferative syndrome. [provided by RefSeq, Aug 2017]","start":53156009,"end":53192717,"strand":1,"description":"protein kinase C delta [Source:HGNC Symbol;Acc:HGNC:9399]"}, {"versioned_ensembl_gene_id":"ENSG00000239256.1","gene_symbol":"AC005412.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29340482,"end":29340822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268499.1","gene_symbol":"AC011479.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38199836,"end":38200934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280679.1","gene_symbol":"AC116165.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23229344,"end":23229859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178163.7","gene_symbol":"ZNF518B","gene_name":"zinc finger protein 518B [Source:HGNC Symbol;Acc:HGNC:29365]","synonyms":"KIAA1729","biotype":"protein_coding","ncbi_id":"85460","summary":null,"start":10439874,"end":10457410,"strand":-1,"description":"zinc finger protein 518B [Source:HGNC Symbol;Acc:HGNC:29365]"}, {"versioned_ensembl_gene_id":"ENSG00000180723.6","gene_symbol":"OR51A9P","gene_name":"olfactory receptor family 51 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15190]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"390039","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4660853,"end":4661763,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15190]"}, {"versioned_ensembl_gene_id":"ENSG00000198870.7","gene_symbol":"STKLD1","gene_name":"serine/threonine kinase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28669]","synonyms":"SGK071,MGC43306,C9orf96","biotype":"protein_coding","ncbi_id":"169436","summary":null,"start":133376367,"end":133406096,"strand":1,"description":"serine/threonine kinase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28669]"}, {"versioned_ensembl_gene_id":"ENSG00000223374.1","gene_symbol":"AC005104.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241351340,"end":241353104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136158.11","gene_symbol":"SPRY2","gene_name":"sprouty RTK signaling antagonist 2 [Source:HGNC Symbol;Acc:HGNC:11270]","synonyms":"hSPRY2","biotype":"protein_coding","ncbi_id":"10253","summary":"This gene encodes a protein belonging to the sprouty family. The encoded protein contains a carboxyl-terminal cysteine-rich domain essential for the inhibitory activity on receptor tyrosine kinase signaling proteins and is required for growth factor stimulated translocation of the protein to membrane ruffles. In primary dermal endothelial cells this gene is transiently upregulated in response to fibroblast growth factor two. This protein is indirectly involved in the non-cell autonomous inhibitory effect on fibroblast growth factor two signaling. The protein interacts with Cas-Br-M (murine) ectropic retroviral transforming sequence, and can function as a bimodal regulator of epidermal growth factor receptor/mitogen-activated protein kinase signaling. This protein may play a role in alveoli branching during lung development as shown by a similar mouse protein. [provided by RefSeq, Jul 2008]","start":80335976,"end":80340951,"strand":-1,"description":"sprouty RTK signaling antagonist 2 [Source:HGNC Symbol;Acc:HGNC:11270]"}, {"versioned_ensembl_gene_id":"ENSG00000198885.9","gene_symbol":"ITPRIPL1","gene_name":"inositol 1,4,5-trisphosphate receptor interacting protein-like 1 [Source:HGNC Symbol;Acc:HGNC:29371]","synonyms":"KIAA1754L","biotype":"protein_coding","ncbi_id":"150771","summary":null,"start":96325331,"end":96330517,"strand":1,"description":"inositol 1,4,5-trisphosphate receptor interacting protein-like 1 [Source:HGNC Symbol;Acc:HGNC:29371]"}, {"versioned_ensembl_gene_id":"ENSG00000271351.1","gene_symbol":"IGKV1OR2-9","gene_name":"immunoglobulin kappa variable 1/OR2-9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5771]","synonyms":"IGKV1/OR2-9","biotype":"IG_V_pseudogene","ncbi_id":"28864","summary":null,"start":97322137,"end":97322423,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5771]"}, {"versioned_ensembl_gene_id":"ENSG00000236718.3","gene_symbol":"RBMY2QP","gene_name":"RNA binding motif protein, Y-linked, family 2, member Q pseudogene [Source:HGNC Symbol;Acc:HGNC:23895]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379006","summary":null,"start":10022489,"end":10034187,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member Q pseudogene [Source:HGNC Symbol;Acc:HGNC:23895]"}, {"versioned_ensembl_gene_id":"ENSG00000180785.9","gene_symbol":"OR51E1","gene_name":"olfactory receptor family 51 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:15194]","synonyms":"OR52A3P,OR51E1P,GPR164,GPR136","biotype":"protein_coding","ncbi_id":"143503","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4643420,"end":4655488,"strand":1,"description":"olfactory receptor family 51 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:15194]"}, {"versioned_ensembl_gene_id":"ENSG00000233566.1","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"dJ25J6.5,C6orf100","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28944738,"end":28945398,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000154556.17","gene_symbol":"SORBS2","gene_name":"sorbin and SH3 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24098]","synonyms":"KIAA0777,ARGBP2","biotype":"protein_coding","ncbi_id":"8470","summary":"Arg and c-Abl represent the mammalian members of the Abelson family of non-receptor protein-tyrosine kinases. They interact with the Arg/Abl binding proteins via the SH3 domains present in the carboxy end of the latter group of proteins. This gene encodes the sorbin and SH3 domain containing 2 protein. It has three C-terminal SH3 domains and an N-terminal sorbin homology (SoHo) domain that interacts with lipid raft proteins. The subcellular localization of this protein in epithelial and cardiac muscle cells suggests that it functions as an adapter protein to assemble signaling complexes in stress fibers, and that it is a potential link between Abl family kinases and the actin cytoskeleton. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":185585444,"end":185956652,"strand":-1,"description":"sorbin and SH3 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24098]"}, {"versioned_ensembl_gene_id":"ENSG00000167779.7","gene_symbol":"IGFBP6","gene_name":"insulin like growth factor binding protein 6 [Source:HGNC Symbol;Acc:HGNC:5475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3489","summary":null,"start":53097436,"end":53102345,"strand":1,"description":"insulin like growth factor binding protein 6 [Source:HGNC Symbol;Acc:HGNC:5475]"}, {"versioned_ensembl_gene_id":"ENSG00000067191.15","gene_symbol":"CACNB1","gene_name":"calcium voltage-gated channel auxiliary subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:1401]","synonyms":"CACNLB1","biotype":"protein_coding","ncbi_id":"782","summary":"The protein encoded by this gene belongs to the calcium channel beta subunit family. It plays an important role in the calcium channel by modulating G protein inhibition, increasing peak calcium current, controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":39173456,"end":39197703,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:1401]"}, {"versioned_ensembl_gene_id":"ENSG00000280355.1","gene_symbol":"AL132656.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79681973,"end":79684094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108244.16","gene_symbol":"KRT23","gene_name":"keratin 23 [Source:HGNC Symbol;Acc:HGNC:6438]","synonyms":"MGC26158,K23,HAIK1,DKFZP434G032,CK23","biotype":"protein_coding","ncbi_id":"25984","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":40922696,"end":40937634,"strand":-1,"description":"keratin 23 [Source:HGNC Symbol;Acc:HGNC:6438]"}, {"versioned_ensembl_gene_id":"ENSG00000259651.2","gene_symbol":"MTCO3P23","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52126]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075182","summary":null,"start":58150275,"end":58150563,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52126]"}, {"versioned_ensembl_gene_id":"ENSG00000216425.4","gene_symbol":"AC004066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105526596,"end":105527397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105738.10","gene_symbol":"SIPA1L3","gene_name":"signal induced proliferation associated 1 like 3 [Source:HGNC Symbol;Acc:HGNC:23801]","synonyms":"KIAA0545","biotype":"protein_coding","ncbi_id":"23094","summary":"This gene belongs to the signal induced proliferation associated 1 family of genes, which encode GTPase-activating proteins specific for the GTP-binding protein Rap1. Rap1 has been implicated in regulation of cell adhesion, cell polarity, and organization of the cytoskeleton. Like other members of the family, the protein encoded by this gene contains RapGAP and PDZ domains. In addition, this protein contains a C-terminal leucine zipper domain. This gene is proposed to function in epithelial cell morphogenesis and establishment or maintenance of polarity. Consistently, expression of the protein in cell culture showed localization to cell-cell borders in apical regions, and downregulation of the gene in 3D Caco2 cell culture resulted in abnormal cell polarity and morphogenesis. Allelic variants of this gene have been associated with congenital cataracts in humans. [provided by RefSeq, Feb 2016]","start":37907228,"end":38208372,"strand":1,"description":"signal induced proliferation associated 1 like 3 [Source:HGNC Symbol;Acc:HGNC:23801]"}, {"versioned_ensembl_gene_id":"ENSG00000277790.1","gene_symbol":"AC084781.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58456188,"end":58456348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269653.1","gene_symbol":"AC011479.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38184376,"end":38186265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235902.1","gene_symbol":"AC108472.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185665885,"end":185675417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249264.1","gene_symbol":"EEF1A1P9","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:3204]","synonyms":"EEF1AL7","biotype":"processed_pseudogene","ncbi_id":"441032","summary":null,"start":105484698,"end":105486080,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:3204]"}, {"versioned_ensembl_gene_id":"ENSG00000224886.2","gene_symbol":"AL132656.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":79684494,"end":79684983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213071.11","gene_symbol":"LPAL2","gene_name":"lipoprotein(a) like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:21210]","synonyms":"APOARGC,APOAL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"80350","summary":"Apolipoprotein(a) is the distinguishing protein moiety of lipoprotein(a), of which elevated plasma levels are correlated with an increased risk of atherosclerosis. This gene is similar to the lipoprotein, Lp(a) gene, but all transcripts produced by this gene contain a truncated open reading frame and are candidates for nonsense-mediated decay. Consequently, this gene is considered to be a pseudogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":160453428,"end":160520269,"strand":-1,"description":"lipoprotein(a) like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:21210]"}, {"versioned_ensembl_gene_id":"ENSG00000186522.14","gene_symbol":"SEPT10","gene_name":"septin 10 [Source:HGNC Symbol;Acc:HGNC:14349]","synonyms":"FLJ11619","biotype":"protein_coding","ncbi_id":"151011","summary":"This gene encodes a member of the septin family of cytoskeletal proteins with GTPase activity. This protein localizes to the cytoplasm and nucleus and displays GTP-binding and GTPase activity. A pseudogene for this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]","start":109542982,"end":109614206,"strand":-1,"description":"septin 10 [Source:HGNC Symbol;Acc:HGNC:14349]"}, {"versioned_ensembl_gene_id":"ENSG00000242244.1","gene_symbol":"ATP5G1P3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39506]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646619","summary":null,"start":138889255,"end":138889957,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39506]"}, {"versioned_ensembl_gene_id":"ENSG00000272447.1","gene_symbol":"AL135925.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79825902,"end":79827602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113812.13","gene_symbol":"ACTR8","gene_name":"ARP8 actin related protein 8 homolog [Source:HGNC Symbol;Acc:HGNC:14672]","synonyms":"INO80N","biotype":"protein_coding","ncbi_id":"93973","summary":null,"start":53867066,"end":53882202,"strand":-1,"description":"ARP8 actin related protein 8 homolog [Source:HGNC Symbol;Acc:HGNC:14672]"}, {"versioned_ensembl_gene_id":"ENSG00000177732.8","gene_symbol":"SOX12","gene_name":"SRY-box 12 [Source:HGNC Symbol;Acc:HGNC:11198]","synonyms":"SOX22","biotype":"protein_coding","ncbi_id":"6666","summary":"Members of the SOX family of transcription factors are characterized by the presence of a DNA-binding high mobility group (HMG) domain, homologous to the HMG box of sex-determining region Y (SRY). Forming a subgroup of the HMG domain superfamily, SOX proteins have been implicated in cell fate decisions in a diverse range of developmental processes. SOX transcription factors have diverse tissue-specific expression patterns during early development and have been proposed to act as target-specific transcription factors and/or as chromatin structure regulatory elements. The protein encoded by this gene was identified as a SOX family member based on conserved domains, and its expression in various tissues suggests a role in both differentiation and maintenance of several cell types. [provided by RefSeq, Jan 2013]","start":325595,"end":330224,"strand":1,"description":"SRY-box 12 [Source:HGNC Symbol;Acc:HGNC:11198]"}, {"versioned_ensembl_gene_id":"ENSG00000248307.5","gene_symbol":"LINC00616","gene_name":"long intergenic non-protein coding RNA 616 [Source:HGNC Symbol;Acc:HGNC:44065]","synonyms":null,"biotype":"lincRNA","ncbi_id":"641365","summary":null,"start":138027422,"end":138130709,"strand":-1,"description":"long intergenic non-protein coding RNA 616 [Source:HGNC Symbol;Acc:HGNC:44065]"}, {"versioned_ensembl_gene_id":"ENSG00000234986.1","gene_symbol":"AL731661.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170695313,"end":170696950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108883.12","gene_symbol":"EFTUD2","gene_name":"elongation factor Tu GTP binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30858]","synonyms":"U5-116KD,Snu114,Snrp116,SNRNP116","biotype":"protein_coding","ncbi_id":"9343","summary":"This gene encodes a GTPase which is a component of the spliceosome complex which processes precursor mRNAs to produce mature mRNAs. Mutations in this gene are associated with mandibulofacial dysostosis with microcephaly. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":44849943,"end":44899662,"strand":-1,"description":"elongation factor Tu GTP binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30858]"}, {"versioned_ensembl_gene_id":"ENSG00000264655.1","gene_symbol":"AC080112.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40367952,"end":40368438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226288.2","gene_symbol":"OR52I2","gene_name":"olfactory receptor family 52 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15221]","synonyms":null,"biotype":"protein_coding","ncbi_id":"143502","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4581743,"end":4593340,"strand":1,"description":"olfactory receptor family 52 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15221]"}, {"versioned_ensembl_gene_id":"ENSG00000110075.14","gene_symbol":"PPP6R3","gene_name":"protein phosphatase 6 regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:1173]","synonyms":"MGC125712,MGC125711,KIAA1558,FLJ43065,FLJ11058,DKFZp781O2362,DKFZp781E2374,DKFZp781E17107,C11orf23,SAPS3,SAPLa,SAPL,SAP190,PP6R3","biotype":"protein_coding","ncbi_id":"55291","summary":"Protein phosphatase regulatory subunits, such as SAPS3, modulate the activity of protein phosphatase catalytic subunits by restricting substrate specificity, recruiting substrates, and determining the intracellular localization of the holoenzyme. SAPS3 is a regulatory subunit for the protein phosphatase-6 catalytic subunit (PPP6C; MIM 612725) (Stefansson and Brautigan, 2006 [PubMed 16769727]).[supplied by OMIM, Nov 2010]","start":68460731,"end":68615334,"strand":1,"description":"protein phosphatase 6 regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:1173]"}, {"versioned_ensembl_gene_id":"ENSG00000239225.1","gene_symbol":"TTTY23","gene_name":"testis-specific transcript, Y-linked 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18847]","synonyms":"NCRNA00148","biotype":"lincRNA","ncbi_id":"252955","summary":null,"start":9910798,"end":9911962,"strand":1,"description":"testis-specific transcript, Y-linked 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18847]"}, {"versioned_ensembl_gene_id":"ENSG00000250033.5","gene_symbol":"SLC7A11-AS1","gene_name":"SLC7A11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44064]","synonyms":"ENST00000512786","biotype":"processed_transcript","ncbi_id":"641364","summary":null,"start":138057464,"end":138178177,"strand":1,"description":"SLC7A11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44064]"}, {"versioned_ensembl_gene_id":"ENSG00000273640.1","gene_symbol":"WBP1LP8","gene_name":"WW domain binding protein 1-like pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51468]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480325","summary":null,"start":170651012,"end":170651338,"strand":-1,"description":"WW domain binding protein 1-like pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51468]"}, {"versioned_ensembl_gene_id":"ENSG00000223405.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bQB10J12.1,bPG70P20.2,TIGD1L,bCX111D4.7","biotype":"processed_transcript","ncbi_id":"414771","summary":null,"start":30856563,"end":30865496,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000255838.1","gene_symbol":"AC069262.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128944274,"end":128945203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225888.1","gene_symbol":"AL805917.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30829032,"end":30837670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260808.1","gene_symbol":"AP003096.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68612899,"end":68616711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236111.5","gene_symbol":"AL603882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45781277,"end":45781957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223970.1","gene_symbol":"AC074397.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53002420,"end":53003429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234304.2","gene_symbol":"SGO1P2","gene_name":"shugoshin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50777]","synonyms":"SGOL1P2","biotype":"processed_pseudogene","ncbi_id":"100533661","summary":null,"start":52891837,"end":52897807,"strand":-1,"description":"shugoshin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50777]"}, {"versioned_ensembl_gene_id":"ENSG00000088053.11","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55013705,"end":55038264,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000228272.1","gene_symbol":"AC106874.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84315108,"end":84350774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215523.7","gene_symbol":"AL773551.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30788147,"end":30820172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243494.1","gene_symbol":"AC011476.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54973817,"end":54974417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226616.1","gene_symbol":"OR52M2P","gene_name":"olfactory receptor family 52 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15226]","synonyms":"OR52M4","biotype":"unprocessed_pseudogene","ncbi_id":"338637","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4514966,"end":4515924,"strand":-1,"description":"olfactory receptor family 52 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15226]"}, {"versioned_ensembl_gene_id":"ENSG00000187657.6","gene_symbol":"TSPY13P","gene_name":"testis specific protein, Y-linked 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:23905]","synonyms":"TSPYP3","biotype":"unprocessed_pseudogene","ncbi_id":"378001","summary":null,"start":9905595,"end":9908139,"strand":-1,"description":"testis specific protein, Y-linked 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:23905]"}, {"versioned_ensembl_gene_id":"ENSG00000224476.3","gene_symbol":"RPL36P16","gene_name":"ribosomal protein L36 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37010]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651600","summary":null,"start":41169861,"end":41170166,"strand":1,"description":"ribosomal protein L36 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37010]"}, {"versioned_ensembl_gene_id":"ENSG00000224133.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"AB023051.1,NCRNA00149","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30756325,"end":30781741,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000261207.1","gene_symbol":"AL031717.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1751559,"end":1752262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275092.1","gene_symbol":"AL031710.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1707252,"end":1707973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213420.7","gene_symbol":"GPC2","gene_name":"glypican 2 [Source:HGNC Symbol;Acc:HGNC:4450]","synonyms":"FLJ38962,DKFZp547M109,cerebroglycan","biotype":"protein_coding","ncbi_id":"221914","summary":null,"start":100169606,"end":100177372,"strand":-1,"description":"glypican 2 [Source:HGNC Symbol;Acc:HGNC:4450]"}, {"versioned_ensembl_gene_id":"ENSG00000181963.5","gene_symbol":"OR52K2","gene_name":"olfactory receptor family 52 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15223]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119774","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4449295,"end":4450361,"strand":1,"description":"olfactory receptor family 52 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15223]"}, {"versioned_ensembl_gene_id":"ENSG00000171999.7","gene_symbol":"OR52P2P","gene_name":"olfactory receptor family 52 subfamily P member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15233]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"119775","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4431323,"end":4432277,"strand":-1,"description":"olfactory receptor family 52 subfamily P member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15233]"}, {"versioned_ensembl_gene_id":"ENSG00000228599.1","gene_symbol":"RPL7P52","gene_name":"ribosomal protein L7 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:35676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646912","summary":null,"start":40106325,"end":40107066,"strand":-1,"description":"ribosomal protein L7 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:35676]"}, {"versioned_ensembl_gene_id":"ENSG00000167550.10","gene_symbol":"RHEBL1","gene_name":"Ras homolog enriched in brain like 1 [Source:HGNC Symbol;Acc:HGNC:21166]","synonyms":"MGC34869,FLJ25797","biotype":"protein_coding","ncbi_id":"121268","summary":null,"start":49064685,"end":49070025,"strand":-1,"description":"Ras homolog enriched in brain like 1 [Source:HGNC Symbol;Acc:HGNC:21166]"}, {"versioned_ensembl_gene_id":"ENSG00000234761.1","gene_symbol":"AC096632.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":202986557,"end":202988582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255011.1","gene_symbol":"AP004607.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90071136,"end":90073055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226676.1","gene_symbol":"BX248123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79628757,"end":79632188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140030.5","gene_symbol":"GPR65","gene_name":"G protein-coupled receptor 65 [Source:HGNC Symbol;Acc:HGNC:4517]","synonyms":"TDAG8,hTDAG8","biotype":"protein_coding","ncbi_id":"8477","summary":null,"start":88005124,"end":88014811,"strand":1,"description":"G protein-coupled receptor 65 [Source:HGNC Symbol;Acc:HGNC:4517]"}, {"versioned_ensembl_gene_id":"ENSG00000182814.7","gene_symbol":"FUNDC2P2","gene_name":"FUN14 domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17247]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"388965","summary":null,"start":84290683,"end":84292202,"strand":1,"description":"FUN14 domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17247]"}, {"versioned_ensembl_gene_id":"ENSG00000241506.1","gene_symbol":"PSMC1P1","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30147]","synonyms":"PSMC1P,bcm3415","biotype":"processed_pseudogene","ncbi_id":"151645","summary":null,"start":68635705,"end":68637024,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30147]"}, {"versioned_ensembl_gene_id":"ENSG00000223709.5","gene_symbol":"TRIM64EP","gene_name":"tripartite motif containing 64E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43975]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440061","summary":null,"start":90057605,"end":90062999,"strand":-1,"description":"tripartite motif containing 64E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43975]"}, {"versioned_ensembl_gene_id":"ENSG00000229210.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SUMO2P,SMT3Bp,dJ271M21,SMT3H2P","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29636014,"end":29636297,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000160445.10","gene_symbol":"ZER1","gene_name":"zyg-11 related cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:30960]","synonyms":"ZYG11BL,ZYG,Hzyg,C9orf60","biotype":"protein_coding","ncbi_id":"10444","summary":"This gene encodes a subunit of an E3 ubiquitin ligase complex that may be involved in meiosis. The encoded protein contains three leucine-rich repeat motifs. [provided by RefSeq, Nov 2012]","start":128729786,"end":128772414,"strand":-1,"description":"zyg-11 related cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:30960]"}, {"versioned_ensembl_gene_id":"ENSG00000171804.10","gene_symbol":"WDR87","gene_name":"WD repeat domain 87 [Source:HGNC Symbol;Acc:HGNC:29934]","synonyms":"NYD-SP11","biotype":"protein_coding","ncbi_id":"83889","summary":null,"start":37884823,"end":37906677,"strand":-1,"description":"WD repeat domain 87 [Source:HGNC Symbol;Acc:HGNC:29934]"}, {"versioned_ensembl_gene_id":"ENSG00000250777.1","gene_symbol":"AC131956.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137690477,"end":137734977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244009.1","gene_symbol":"B3GAT3P1","gene_name":"beta-1,3-glucuronyltransferase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35243]","synonyms":"PSIGLCAT-I,B3GAT3P","biotype":"processed_pseudogene","ncbi_id":"402146","summary":null,"start":160452598,"end":160453403,"strand":1,"description":"beta-1,3-glucuronyltransferase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35243]"}, {"versioned_ensembl_gene_id":"ENSG00000251338.1","gene_symbol":"AC006499.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10294463,"end":10295579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267089.1","gene_symbol":"AC008543.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11841241,"end":11842439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224627.1","gene_symbol":"RPL37P10","gene_name":"ribosomal protein L37 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271015","summary":null,"start":83594956,"end":83595243,"strand":1,"description":"ribosomal protein L37 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36951]"}, {"versioned_ensembl_gene_id":"ENSG00000248203.1","gene_symbol":"AC011362.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103246048,"end":103253519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168275.14","gene_symbol":"COA6","gene_name":"cytochrome c oxidase assembly factor 6 [Source:HGNC Symbol;Acc:HGNC:18025]","synonyms":"C1orf31","biotype":"protein_coding","ncbi_id":"388753","summary":"This gene encodes a member of the cytochrome c oxidase subunit 6B family. The encoded protein associates with cytochrome c oxidase may act has an cytochrome c oxidase mitochondrial respiratory complex VI assembly factor. Mutations in this gene may be associated with fatal infantile cardiomyopathy. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":234373456,"end":234384049,"strand":1,"description":"cytochrome c oxidase assembly factor 6 [Source:HGNC Symbol;Acc:HGNC:18025]"}, {"versioned_ensembl_gene_id":"ENSG00000247315.3","gene_symbol":"ZCCHC3","gene_name":"zinc finger CCHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:16230]","synonyms":"C20orf99,dJ1103G7.7","biotype":"protein_coding","ncbi_id":"85364","summary":null,"start":296968,"end":300321,"strand":1,"description":"zinc finger CCHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:16230]"}, {"versioned_ensembl_gene_id":"ENSG00000259641.5","gene_symbol":"PCAT29","gene_name":"prostate cancer associated transcript 29 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50895]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104472713","summary":"This gene is thought to produce a functional long non-coding RNA. This transcript was identified in prostate cancer cells and may suppress tumor formation. [provided by RefSeq, Feb 2015]","start":69592129,"end":69695750,"strand":1,"description":"prostate cancer associated transcript 29 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50895]"}, {"versioned_ensembl_gene_id":"ENSG00000235605.1","gene_symbol":"AL355472.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":234356704,"end":234357141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270691.1","gene_symbol":"AL161912.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79850871,"end":79851498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265359.1","gene_symbol":"AC004231.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40850800,"end":40863282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236225.1","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCG4P10,HCGIV.9,HCGIV-10","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29791993,"end":29792967,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000187242.4","gene_symbol":"KRT12","gene_name":"keratin 12 [Source:HGNC Symbol;Acc:HGNC:6414]","synonyms":"K12","biotype":"protein_coding","ncbi_id":"3859","summary":"KRT12 encodes the type I intermediate filament chain keratin 12, expressed in corneal epithelia. Mutations in this gene lead to Meesmann corneal dystrophy. [provided by RefSeq, Jul 2008]","start":40861303,"end":40867210,"strand":-1,"description":"keratin 12 [Source:HGNC Symbol;Acc:HGNC:6414]"}, {"versioned_ensembl_gene_id":"ENSG00000283400.1","gene_symbol":"AL807740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20443326,"end":20492349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180098.9","gene_symbol":"TRNAU1AP","gene_name":"tRNA selenocysteine 1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30813]","synonyms":"TRSPAP1,SECP43,FLJ20503","biotype":"protein_coding","ncbi_id":"54952","summary":null,"start":28553085,"end":28578545,"strand":1,"description":"tRNA selenocysteine 1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30813]"}, {"versioned_ensembl_gene_id":"ENSG00000087076.8","gene_symbol":"HSD17B14","gene_name":"hydroxysteroid 17-beta dehydrogenase 14 [Source:HGNC Symbol;Acc:HGNC:23238]","synonyms":"retSDR3,SDR47C1,DHRS10","biotype":"protein_coding","ncbi_id":"51171","summary":"17-beta-hydroxysteroid dehydrogenases, such as HSD17B14, are primarily involved in metabolism of steroids at the C17 position and also of other substrates, such as fatty acids, prostaglandins, and xenobiotics (Lukacik et al., 2007 [PubMed 17067289]).[supplied by OMIM, Jun 2009]","start":48813017,"end":48836678,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 14 [Source:HGNC Symbol;Acc:HGNC:23238]"}, {"versioned_ensembl_gene_id":"ENSG00000237272.2","gene_symbol":"OR51R1P","gene_name":"olfactory receptor family 51 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15203]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"390034","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4418060,"end":4419011,"strand":1,"description":"olfactory receptor family 51 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15203]"}, {"versioned_ensembl_gene_id":"ENSG00000106976.20","gene_symbol":"DNM1","gene_name":"dynamin 1 [Source:HGNC Symbol;Acc:HGNC:2972]","synonyms":"DNM","biotype":"protein_coding","ncbi_id":"1759","summary":"This gene encodes a member of the dynamin subfamily of GTP-binding proteins. The encoded protein possesses unique mechanochemical properties used to tubulate and sever membranes, and is involved in clathrin-mediated endocytosis and other vesicular trafficking processes. Actin and other cytoskeletal proteins act as binding partners for the encoded protein, which can also self-assemble leading to stimulation of GTPase activity. More than sixty highly conserved copies of the 3' region of this gene are found elsewhere in the genome, particularly on chromosomes Y and 15. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":128191655,"end":128255248,"strand":1,"description":"dynamin 1 [Source:HGNC Symbol;Acc:HGNC:2972]"}, {"versioned_ensembl_gene_id":"ENSG00000167634.12","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"CLR19.4,NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54923509,"end":54966312,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000228622.1","gene_symbol":"Z82198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33105383,"end":33106059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135297.15","gene_symbol":"MTO1","gene_name":"mitochondrial tRNA translation optimization 1 [Source:HGNC Symbol;Acc:HGNC:19261]","synonyms":null,"biotype":"protein_coding","ncbi_id":"25821","summary":"This gene encodes a mitochondrial protein thought to be involved in mitochondrial tRNA modification. The encoded protein may also play a role in the expression of the non-syndromic and aminoglycoside-induced deafness phenotypes associated with a specific mutation in the mitochondrial 12S rRNA gene. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":73461578,"end":73509236,"strand":1,"description":"mitochondrial tRNA translation optimization 1 [Source:HGNC Symbol;Acc:HGNC:19261]"}, {"versioned_ensembl_gene_id":"ENSG00000232091.1","gene_symbol":"PNLIPP1","gene_name":"pancreatic lipase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45264]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419068","summary":null,"start":116577308,"end":116583317,"strand":1,"description":"pancreatic lipase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45264]"}, {"versioned_ensembl_gene_id":"ENSG00000275392.1","gene_symbol":"AL445493.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":207127010,"end":207127486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000041880.14","gene_symbol":"PARP3","gene_name":"poly(ADP-ribose) polymerase family member 3 [Source:HGNC Symbol;Acc:HGNC:273]","synonyms":"ADPRTL3,ADPRT3,pADPRT-3,IRT1,hPARP-3","biotype":"protein_coding","ncbi_id":"10039","summary":"The protein encoded by this gene belongs to the PARP family. These enzymes modify nuclear proteins by poly-ADP-ribosylation, which is required for DNA repair, regulation of apoptosis, and maintenance of genomic stability. This gene encodes the poly(ADP-ribosyl)transferase 3, which is preferentially localized to the daughter centriole throughout the cell cycle. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":51942345,"end":51948867,"strand":1,"description":"poly(ADP-ribose) polymerase family member 3 [Source:HGNC Symbol;Acc:HGNC:273]"}, {"versioned_ensembl_gene_id":"ENSG00000283695.1","gene_symbol":"AC010487.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52865369,"end":52865429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254381.3","gene_symbol":"TUBB8P5","gene_name":"tubulin beta 8 class VIII pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42186]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"121014","summary":null,"start":38201566,"end":38203792,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42186]"}, {"versioned_ensembl_gene_id":"ENSG00000133477.16","gene_symbol":"FAM83F","gene_name":"family with sequence similarity 83 member F [Source:HGNC Symbol;Acc:HGNC:25148]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113828","summary":null,"start":39994949,"end":40043529,"strand":1,"description":"family with sequence similarity 83 member F [Source:HGNC Symbol;Acc:HGNC:25148]"}, {"versioned_ensembl_gene_id":"ENSG00000253187.2","gene_symbol":"HOXA10-AS","gene_name":"HOXA10 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40281]","synonyms":"HOXA-AS4","biotype":"antisense_RNA","ncbi_id":"100874323","summary":null,"start":27168619,"end":27171915,"strand":1,"description":"HOXA10 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40281]"}, {"versioned_ensembl_gene_id":"ENSG00000277007.1","gene_symbol":"AC096642.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219270774,"end":219273387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254785.1","gene_symbol":"AP005435.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89895799,"end":89900449,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125962.14","gene_symbol":"ARMCX5","gene_name":"armadillo repeat containing, X-linked 5 [Source:HGNC Symbol;Acc:HGNC:25772]","synonyms":"GASP5,FLJ12969","biotype":"protein_coding","ncbi_id":"64860","summary":null,"start":102599168,"end":102604159,"strand":1,"description":"armadillo repeat containing, X-linked 5 [Source:HGNC Symbol;Acc:HGNC:25772]"}, {"versioned_ensembl_gene_id":"ENSG00000183153.6","gene_symbol":"GJD3","gene_name":"gap junction protein delta 3 [Source:HGNC Symbol;Acc:HGNC:19147]","synonyms":"GJC1,GJA11,CX31.9,Cx30.2","biotype":"protein_coding","ncbi_id":"125111","summary":"This gene is a member of the large family of connexins that are required for the formation of gap junctions. Six connexin monomers form a hemichannel, or connexon, on the cell surface. This connexon can interact with a connexon from a neighboring cell, thus forming a channel linking the cytoplasm of the 2 cells. [provided by RefSeq, Jul 2008]","start":40362931,"end":40363815,"strand":-1,"description":"gap junction protein delta 3 [Source:HGNC Symbol;Acc:HGNC:19147]"}, {"versioned_ensembl_gene_id":"ENSG00000266208.1","gene_symbol":"AC080112.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40360655,"end":40364693,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057593.13","gene_symbol":"F7","gene_name":"coagulation factor VII [Source:HGNC Symbol;Acc:HGNC:3544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2155","summary":"This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Defects in this gene can cause coagulopathy. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015]","start":113105788,"end":113120681,"strand":1,"description":"coagulation factor VII [Source:HGNC Symbol;Acc:HGNC:3544]"}, {"versioned_ensembl_gene_id":"ENSG00000255055.1","gene_symbol":"MTND1P35","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:42088]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480433","summary":null,"start":89908540,"end":89909047,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:42088]"}, {"versioned_ensembl_gene_id":"ENSG00000223417.8","gene_symbol":"TRIM49D1","gene_name":"tripartite motif containing 49D1 [Source:HGNC Symbol;Acc:HGNC:43973]","synonyms":"TRIM49DP,TRIM49D1P,TRIM49D","biotype":"protein_coding","ncbi_id":"399939","summary":null,"start":89911111,"end":89921767,"strand":-1,"description":"tripartite motif containing 49D1 [Source:HGNC Symbol;Acc:HGNC:43973]"}, {"versioned_ensembl_gene_id":"ENSG00000237289.9","gene_symbol":"CKMT1B","gene_name":"creatine kinase, mitochondrial 1B [Source:HGNC Symbol;Acc:HGNC:1995]","synonyms":"UMTCK,CKMT1,CKMT","biotype":"protein_coding","ncbi_id":"1159","summary":"Mitochondrial creatine (MtCK) kinase is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine. It belongs to the creatine kinase isoenzyme family. It exists as two isoenzymes, sarcomeric MtCK and ubiquitous MtCK, encoded by separate genes. Mitochondrial creatine kinase occurs in two different oligomeric forms: dimers and octamers, in contrast to the exclusively dimeric cytosolic creatine kinase isoenzymes. Many malignant cancers with poor prognosis have shown overexpression of ubiquitous mitochondrial creatine kinase; this may be related to high energy turnover and failure to eliminate cancer cells via apoptosis. Ubiquitous mitochondrial creatine kinase has 80% homology with the coding exons of sarcomeric mitochondrial creatine kinase. Two genes located near each other on chromosome 15 have been identified which encode identical mitochondrial creatine kinase proteins. [provided by RefSeq, Jul 2008]","start":43593054,"end":43604901,"strand":1,"description":"creatine kinase, mitochondrial 1B [Source:HGNC Symbol;Acc:HGNC:1995]"}, {"versioned_ensembl_gene_id":"ENSG00000271147.7","gene_symbol":"ARMCX5-GPRASP2","gene_name":"ARMCX5-GPRASP2 readthrough [Source:HGNC Symbol;Acc:HGNC:42000]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100528062","summary":"This locus represents naturally occurring readthrough transcription among the adjacent armadillo repeat containing, X-linked 5 (ARMCX5), G protein-coupled receptor associated sorting proteins 1 and 2 (GPRASP1 and GPRASP2), basic helix-loop-helix family member b9 (BHLHB9), and long intergenic non-protein coding RNA 630 (LINC00630) genes on chromosome X. Transcripts may make use of multiple alternative promoters and polyadenylation signals in this region. Readthrough transcripts may produce proteins identical to the proteins encoded by GPRASP2 or BHLHB9. [provided by RefSeq, Apr 2017]","start":102599512,"end":102714671,"strand":1,"description":"ARMCX5-GPRASP2 readthrough [Source:HGNC Symbol;Acc:HGNC:42000]"}, {"versioned_ensembl_gene_id":"ENSG00000255003.1","gene_symbol":"CYCSP28","gene_name":"cytochrome c, somatic pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:24402]","synonyms":"HCP28","biotype":"processed_pseudogene","ncbi_id":"360179","summary":null,"start":83328926,"end":83329246,"strand":1,"description":"cytochrome c, somatic pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:24402]"}, {"versioned_ensembl_gene_id":"ENSG00000254676.1","gene_symbol":"AP000873.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":83180144,"end":83184520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269939.1","gene_symbol":"PCF11-AS1","gene_name":"PCF11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52263]","synonyms":"ENST00000602322.1","biotype":"lincRNA","ncbi_id":"106736475","summary":null,"start":83185521,"end":83187036,"strand":-1,"description":"PCF11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52263]"}, {"versioned_ensembl_gene_id":"ENSG00000166169.16","gene_symbol":"POLL","gene_name":"DNA polymerase lambda [Source:HGNC Symbol;Acc:HGNC:9184]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27343","summary":"This gene encodes a DNA polymerase. DNA polymerases catalyze DNA-template-directed extension of the 3'-end of a DNA strand. This particular polymerase, which is a member of the X family of DNA polymerases, likely plays a role in non-homologous end joining and other DNA repair processes. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2010]","start":101578882,"end":101588270,"strand":-1,"description":"DNA polymerase lambda [Source:HGNC Symbol;Acc:HGNC:9184]"}, {"versioned_ensembl_gene_id":"ENSG00000247137.8","gene_symbol":"AP000873.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":83184491,"end":83193794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278346.1","gene_symbol":"AC080112.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40380666,"end":40381838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185800.11","gene_symbol":"DMWD","gene_name":"DM1 locus, WD repeat containing [Source:HGNC Symbol;Acc:HGNC:2936]","synonyms":"gene59,DMR-N9,D19S593E","biotype":"protein_coding","ncbi_id":"1762","summary":null,"start":45782947,"end":45792802,"strand":-1,"description":"DM1 locus, WD repeat containing [Source:HGNC Symbol;Acc:HGNC:2936]"}, {"versioned_ensembl_gene_id":"ENSG00000260132.1","gene_symbol":"AL032819.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1408834,"end":1412248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233802.8","gene_symbol":"TRIM49D2","gene_name":"tripartite motif containing 49D2 [Source:HGNC Symbol;Acc:HGNC:37217]","synonyms":"TRIM49L1,TRIM49L,TRIM49D2P","biotype":"protein_coding","ncbi_id":"729384","summary":null,"start":89924064,"end":89933063,"strand":1,"description":"tripartite motif containing 49D2 [Source:HGNC Symbol;Acc:HGNC:37217]"}, {"versioned_ensembl_gene_id":"ENSG00000059145.18","gene_symbol":"UNKL","gene_name":"unkempt family like zinc finger [Source:HGNC Symbol;Acc:HGNC:14184]","synonyms":"ZC3HDC5L,ZC3H5L,FLJ23360,C16orf28","biotype":"protein_coding","ncbi_id":"64718","summary":"This gene encodes a RING finger protein that may function in Rac signaling. It can bind to Brg/Brm-associated factor 60b and can promote its ubiquitination. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":1363205,"end":1414751,"strand":-1,"description":"unkempt family like zinc finger [Source:HGNC Symbol;Acc:HGNC:14184]"}, {"versioned_ensembl_gene_id":"ENSG00000160293.16","gene_symbol":"VAV2","gene_name":"vav guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:12658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7410","summary":"VAV2 is the second member of the VAV guanine nucleotide exchange factor family of oncogenes. Unlike VAV1, which is expressed exclusively in hematopoietic cells, VAV2 transcripts were found in most tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":133761894,"end":133992604,"strand":-1,"description":"vav guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:12658]"}, {"versioned_ensembl_gene_id":"ENSG00000230320.1","gene_symbol":"BEND7P1","gene_name":"BEN domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419793","summary":null,"start":102705784,"end":102706240,"strand":1,"description":"BEN domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51362]"}, {"versioned_ensembl_gene_id":"ENSG00000255541.1","gene_symbol":"AP000873.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83209399,"end":83209634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270050.1","gene_symbol":"AL035427.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102599657,"end":102659712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254818.1","gene_symbol":"AP004607.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89944035,"end":89949402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270182.1","gene_symbol":"AC004080.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27158344,"end":27158976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273002.1","gene_symbol":"AL355388.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155978799,"end":155982986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278837.1","gene_symbol":"AP004607.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89954593,"end":89954908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137500.9","gene_symbol":"CCDC90B","gene_name":"coiled-coil domain containing 90B [Source:HGNC Symbol;Acc:HGNC:28108]","synonyms":"MDS025,MDS011","biotype":"protein_coding","ncbi_id":"60492","summary":null,"start":83259097,"end":83286407,"strand":-1,"description":"coiled-coil domain containing 90B [Source:HGNC Symbol;Acc:HGNC:28108]"}, {"versioned_ensembl_gene_id":"ENSG00000228965.1","gene_symbol":"RPSAP60","gene_name":"ribosomal protein SA pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:36331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271149","summary":null,"start":152045314,"end":152046193,"strand":-1,"description":"ribosomal protein SA pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:36331]"}, {"versioned_ensembl_gene_id":"ENSG00000241737.2","gene_symbol":"FAM90A23P","gene_name":"family with sequence similarity 90 member A23, pseudogene [Source:HGNC Symbol;Acc:HGNC:32271]","synonyms":"FAM90A23","biotype":"unprocessed_pseudogene","ncbi_id":"645572","summary":null,"start":7579644,"end":7582653,"strand":-1,"description":"family with sequence similarity 90 member A23, pseudogene [Source:HGNC Symbol;Acc:HGNC:32271]"}, {"versioned_ensembl_gene_id":"ENSG00000229637.3","gene_symbol":"PRAC2","gene_name":"prostate cancer susceptibility candidate 2 [Source:HGNC Symbol;Acc:HGNC:30143]","synonyms":"NCRNA00253,HOXB13-AS1,HOXB-AS5,C17orf93","biotype":"protein_coding","ncbi_id":"360205","summary":"This gene is highly expressed in prostate, rectum, colon, and testis. This gene may produce a non-coding RNA or may encode a short protein that might localize to the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":48723168,"end":48724758,"strand":1,"description":"prostate cancer susceptibility candidate 2 [Source:HGNC Symbol;Acc:HGNC:30143]"}, {"versioned_ensembl_gene_id":"ENSG00000250147.1","gene_symbol":"MORF4L2P1","gene_name":"mortality factor 4 like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20403]","synonyms":"MRG4,MORF4LP4","biotype":"processed_pseudogene","ncbi_id":"643915","summary":null,"start":54086926,"end":54087783,"strand":1,"description":"mortality factor 4 like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20403]"}, {"versioned_ensembl_gene_id":"ENSG00000276443.1","gene_symbol":"PVT1_1","gene_name":"Pvt1 oncogene conserved region 1 [Source:RFAM;Acc:RF02164]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127794541,"end":127794734,"strand":1,"description":"Pvt1 oncogene conserved region 1 [Source:RFAM;Acc:RF02164]"}, {"versioned_ensembl_gene_id":"ENSG00000129028.8","gene_symbol":"THAP10","gene_name":"THAP domain containing 10 [Source:HGNC Symbol;Acc:HGNC:23193]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56906","summary":"This gene encodes a member of a family of proteins sharing an N-terminal Thanatos-associated domain. The Thanatos-associated domain contains a zinc finger signature similar to DNA-binding domains. This gene is part of a bidirectional gene pair on the long arm of chromosome 15 that is regulated by estrogen and may play a role in breast cancer. [provided by RefSeq, Nov 2010]","start":70881342,"end":70892785,"strand":-1,"description":"THAP domain containing 10 [Source:HGNC Symbol;Acc:HGNC:23193]"}, {"versioned_ensembl_gene_id":"ENSG00000274231.1","gene_symbol":"AC134878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11144250,"end":11144492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167721.10","gene_symbol":"TSR1","gene_name":"TSR1, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:25542]","synonyms":"FLJ10534","biotype":"protein_coding","ncbi_id":"55720","summary":null,"start":2322503,"end":2337507,"strand":-1,"description":"TSR1, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:25542]"}, {"versioned_ensembl_gene_id":"ENSG00000212163.5","gene_symbol":"SNORD91A","gene_name":"small nucleolar RNA, C/D box 91A [Source:HGNC Symbol;Acc:HGNC:32752]","synonyms":"HBII-296a","biotype":"snoRNA","ncbi_id":"692207","summary":null,"start":2330180,"end":2330370,"strand":-1,"description":"small nucleolar RNA, C/D box 91A [Source:HGNC Symbol;Acc:HGNC:32752]"}, {"versioned_ensembl_gene_id":"ENSG00000262810.1","gene_symbol":"AC090617.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2089681,"end":2101560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225477.3","gene_symbol":"AC099730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21283779,"end":21284955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129910.7","gene_symbol":"CDH15","gene_name":"cadherin 15 [Source:HGNC Symbol;Acc:HGNC:1754]","synonyms":"CDH3,CDH14","biotype":"protein_coding","ncbi_id":"1013","summary":"This gene is a member of the cadherin superfamily of genes, encoding calcium-dependent intercellular adhesion glycoproteins. Cadherins consist of an extracellular domain containing 5 cadherin domains, a transmembrane region, and a conserved cytoplasmic domain. Transcripts from this particular cadherin are expressed in myoblasts and upregulated in myotubule-forming cells. The protein is thought to be essential for the control of morphogenetic processes, specifically myogenesis, and may provide a trigger for terminal muscle cell differentiation. [provided by RefSeq, Jul 2008]","start":89171767,"end":89195492,"strand":1,"description":"cadherin 15 [Source:HGNC Symbol;Acc:HGNC:1754]"}, {"versioned_ensembl_gene_id":"ENSG00000204873.4","gene_symbol":"KRTAP9-3","gene_name":"keratin associated protein 9-3 [Source:HGNC Symbol;Acc:HGNC:16927]","synonyms":"KAP9.3","biotype":"protein_coding","ncbi_id":"83900","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41232463,"end":41233454,"strand":1,"description":"keratin associated protein 9-3 [Source:HGNC Symbol;Acc:HGNC:16927]"}, {"versioned_ensembl_gene_id":"ENSG00000254906.1","gene_symbol":"AC090707.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20670425,"end":20671297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275521.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54906121,"end":54910036,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000255515.1","gene_symbol":"AP003499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93609760,"end":93610333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254730.1","gene_symbol":"AP002453.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108727741,"end":108730104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248300.1","gene_symbol":"LINC02360","gene_name":"long intergenic non-protein coding RNA 2360 [Source:HGNC Symbol;Acc:HGNC:53282]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374484","summary":null,"start":11740948,"end":11769468,"strand":-1,"description":"long intergenic non-protein coding RNA 2360 [Source:HGNC Symbol;Acc:HGNC:53282]"}, {"versioned_ensembl_gene_id":"ENSG00000180929.5","gene_symbol":"GPR62","gene_name":"G protein-coupled receptor 62 [Source:HGNC Symbol;Acc:HGNC:13301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"118442","summary":null,"start":51955314,"end":51957504,"strand":1,"description":"G protein-coupled receptor 62 [Source:HGNC Symbol;Acc:HGNC:13301]"}, {"versioned_ensembl_gene_id":"ENSG00000198271.4","gene_symbol":"KRTAP4-5","gene_name":"keratin associated protein 4-5 [Source:HGNC Symbol;Acc:HGNC:18899]","synonyms":"KAP4.5","biotype":"protein_coding","ncbi_id":"85289","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41148924,"end":41149802,"strand":-1,"description":"keratin associated protein 4-5 [Source:HGNC Symbol;Acc:HGNC:18899]"}, {"versioned_ensembl_gene_id":"ENSG00000214026.10","gene_symbol":"MRPL23","gene_name":"mitochondrial ribosomal protein L23 [Source:HGNC Symbol;Acc:HGNC:10322]","synonyms":"RPL23L,L23MRP","biotype":"protein_coding","ncbi_id":"6150","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. The gene is biallelically expressed, despite its location within a region of imprinted genes on chromosome 11. [provided by RefSeq, Jul 2008]","start":1947278,"end":1984522,"strand":1,"description":"mitochondrial ribosomal protein L23 [Source:HGNC Symbol;Acc:HGNC:10322]"}, {"versioned_ensembl_gene_id":"ENSG00000002587.9","gene_symbol":"HS3ST1","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5194]","synonyms":"3OST1","biotype":"protein_coding","ncbi_id":"9957","summary":"Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. The enzyme encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. It possesses both heparan sulfate glucosaminyl 3-O-sulfotransferase activity, anticoagulant heparan sulfate conversion activity, and is a rate limiting enzyme for synthesis of anticoagulant heparan. This enzyme is an intraluminal Golgi resident protein. [provided by RefSeq, Jul 2008]","start":11393150,"end":11429765,"strand":-1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5194]"}, {"versioned_ensembl_gene_id":"ENSG00000251152.1","gene_symbol":"AC025539.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11469250,"end":11478196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250896.1","gene_symbol":"RNPS1P1","gene_name":"RNA binding protein with serine rich domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39525]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643446","summary":null,"start":11371975,"end":11372892,"strand":1,"description":"RNA binding protein with serine rich domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39525]"}, {"versioned_ensembl_gene_id":"ENSG00000275084.3","gene_symbol":"SNORD91B","gene_name":"small nucleolar RNA, C/D box 91B [Source:HGNC Symbol;Acc:HGNC:32753]","synonyms":"HBII-296b","biotype":"snoRNA","ncbi_id":"692208","summary":null,"start":2329016,"end":2329237,"strand":-1,"description":"small nucleolar RNA, C/D box 91B [Source:HGNC Symbol;Acc:HGNC:32753]"}, {"versioned_ensembl_gene_id":"ENSG00000242732.4","gene_symbol":"RTL5","gene_name":"retrotransposon Gag like 5 [Source:HGNC Symbol;Acc:HGNC:29430]","synonyms":"SIRH8,RGAG4,Mart5,Mar5,KIAA2001","biotype":"protein_coding","ncbi_id":"340526","summary":null,"start":72127110,"end":72131901,"strand":-1,"description":"retrotransposon Gag like 5 [Source:HGNC Symbol;Acc:HGNC:29430]"}, {"versioned_ensembl_gene_id":"ENSG00000198429.9","gene_symbol":"ZNF69","gene_name":"zinc finger protein 69 [Source:HGNC Symbol;Acc:HGNC:13138]","synonyms":"Cos5","biotype":"protein_coding","ncbi_id":"7620","summary":null,"start":11887784,"end":11914329,"strand":1,"description":"zinc finger protein 69 [Source:HGNC Symbol;Acc:HGNC:13138]"}, {"versioned_ensembl_gene_id":"ENSG00000200112.1","gene_symbol":"SNORD56","gene_name":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]","synonyms":"U56,RNU56","biotype":"snoRNA","ncbi_id":"26793","summary":null,"start":115852648,"end":115852718,"strand":-1,"description":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]"}, {"versioned_ensembl_gene_id":"ENSG00000113302.4","gene_symbol":"IL12B","gene_name":"interleukin 12B [Source:HGNC Symbol;Acc:HGNC:5970]","synonyms":"NKSF2,NKSF,IL-12B,CLMF2,CLMF","biotype":"protein_coding","ncbi_id":"3593","summary":"This gene encodes a subunit of interleukin 12, a cytokine that acts on T and natural killer cells, and has a broad array of biological activities. Interleukin 12 is a disulfide-linked heterodimer composed of the 40 kD cytokine receptor like subunit encoded by this gene, and a 35 kD subunit encoded by IL12A. This cytokine is expressed by activated macrophages that serve as an essential inducer of Th1 cells development. This cytokine has been found to be important for sustaining a sufficient number of memory/effector Th1 cells to mediate long-term protection to an intracellular pathogen. Overexpression of this gene was observed in the central nervous system of patients with multiple sclerosis (MS), suggesting a role of this cytokine in the pathogenesis of the disease. The promoter polymorphism of this gene has been reported to be associated with the severity of atopic and non-atopic asthma in children. [provided by RefSeq, Jul 2008]","start":159314783,"end":159330887,"strand":-1,"description":"interleukin 12B [Source:HGNC Symbol;Acc:HGNC:5970]"}, {"versioned_ensembl_gene_id":"ENSG00000236598.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":29993130,"end":30054145,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000175711.8","gene_symbol":"B3GNTL1","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:21727]","synonyms":"B3GNT8","biotype":"protein_coding","ncbi_id":"146712","summary":null,"start":82942155,"end":83051810,"strand":-1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:21727]"}, {"versioned_ensembl_gene_id":"ENSG00000262663.1","gene_symbol":"AC087222.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82918282,"end":82918785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250803.6","gene_symbol":"AC010255.3","gene_name":"uncharacterized protein LOC100505841 [Source:RefSeq peptide;Acc:NP_001182464]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":122129622,"end":122183949,"strand":1,"description":"uncharacterized protein LOC100505841 [Source:RefSeq peptide;Acc:NP_001182464]"}, {"versioned_ensembl_gene_id":"ENSG00000130255.12","gene_symbol":"RPL36","gene_name":"ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:13631]","synonyms":"L36,DKFZp566B023","biotype":"protein_coding","ncbi_id":"25873","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L36E family of ribosomal proteins. It is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":5674947,"end":5691876,"strand":1,"description":"ribosomal protein L36 [Source:HGNC Symbol;Acc:HGNC:13631]"}, {"versioned_ensembl_gene_id":"ENSG00000237074.2","gene_symbol":"AL596218.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207240122,"end":207309292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186350.9","gene_symbol":"RXRA","gene_name":"retinoid X receptor alpha [Source:HGNC Symbol;Acc:HGNC:10477]","synonyms":"NR2B1","biotype":"protein_coding","ncbi_id":"6256","summary":"Retinoid X receptors (RXRs) and retinoic acid receptors (RARs) are nuclear receptors that mediate the biological effects of retinoids by their involvement in retinoic acid-mediated gene activation. These receptors function as transcription factors by binding as homodimers or heterodimers to specific sequences in the promoters of target genes. The protein encoded by this gene is a member of the steroid and thyroid hormone receptor superfamily of transcriptional regulators. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]","start":134317098,"end":134440585,"strand":1,"description":"retinoid X receptor alpha [Source:HGNC Symbol;Acc:HGNC:10477]"}, {"versioned_ensembl_gene_id":"ENSG00000262652.1","gene_symbol":"AC124283.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":82578023,"end":82578616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240416.1","gene_symbol":"CYCSP20","gene_name":"cytochrome c, somatic pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:24394]","synonyms":"HCP20","biotype":"processed_pseudogene","ncbi_id":"349158","summary":null,"start":129117513,"end":129117827,"strand":-1,"description":"cytochrome c, somatic pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:24394]"}, {"versioned_ensembl_gene_id":"ENSG00000276455.1","gene_symbol":"AC138747.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28349050,"end":28358014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237099.1","gene_symbol":"GYG1P2","gene_name":"glycogenin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39710]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647317","summary":null,"start":82823131,"end":82824136,"strand":1,"description":"glycogenin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39710]"}, {"versioned_ensembl_gene_id":"ENSG00000273051.1","gene_symbol":"AC103710.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4752046,"end":4752944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238005.2","gene_symbol":"AL391832.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234957342,"end":234970062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223798.1","gene_symbol":"CR759960.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29998237,"end":29999232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258016.1","gene_symbol":"HIGD1AP1","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22804]","synonyms":"HIGD1DP,HIGD1D","biotype":"processed_pseudogene","ncbi_id":"100129086","summary":null,"start":53142053,"end":53142327,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22804]"}, {"versioned_ensembl_gene_id":"ENSG00000282054.1","gene_symbol":"AC229888.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142561449,"end":142562408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231602.1","gene_symbol":"RPL35AP4","gene_name":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]","synonyms":"BPG294E21.7,OTTHUMG00000140156","biotype":"processed_pseudogene","ncbi_id":"100048922","summary":null,"start":33559730,"end":33559831,"strand":-1,"description":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]"}, {"versioned_ensembl_gene_id":"ENSG00000232411.1","gene_symbol":"AC009495.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165833048,"end":165839098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259691.2","gene_symbol":"FKBP1AP2","gene_name":"FK506 binding protein 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3715]","synonyms":"FKBP1P2","biotype":"processed_pseudogene","ncbi_id":"2283","summary":null,"start":73143236,"end":73143518,"strand":-1,"description":"FK506 binding protein 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3715]"}, {"versioned_ensembl_gene_id":"ENSG00000226101.1","gene_symbol":"LINC02097","gene_name":"long intergenic non-protein coding RNA 2097 [Source:HGNC Symbol;Acc:HGNC:52948]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928205","summary":null,"start":72072333,"end":72093481,"strand":1,"description":"long intergenic non-protein coding RNA 2097 [Source:HGNC Symbol;Acc:HGNC:52948]"}, {"versioned_ensembl_gene_id":"ENSG00000228639.6","gene_symbol":"LINC02095","gene_name":"long intergenic non-protein coding RNA 2095 [Source:HGNC Symbol;Acc:HGNC:52946]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723505","summary":null,"start":72021851,"end":72034092,"strand":-1,"description":"long intergenic non-protein coding RNA 2095 [Source:HGNC Symbol;Acc:HGNC:52946]"}, {"versioned_ensembl_gene_id":"ENSG00000271862.1","gene_symbol":"AC104118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83049376,"end":83050964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249664.1","gene_symbol":"AC027338.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83012285,"end":83013109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187513.8","gene_symbol":"GJA4","gene_name":"gap junction protein alpha 4 [Source:HGNC Symbol;Acc:HGNC:4278]","synonyms":"CX37","biotype":"protein_coding","ncbi_id":"2701","summary":"This gene encodes a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene have been associated with atherosclerosis and a higher risk of myocardial infarction. [provided by RefSeq, Jul 2008]","start":34792998,"end":34795747,"strand":1,"description":"gap junction protein alpha 4 [Source:HGNC Symbol;Acc:HGNC:4278]"}, {"versioned_ensembl_gene_id":"ENSG00000250577.1","gene_symbol":"AC109927.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138923930,"end":138924232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244398.1","gene_symbol":"AC116533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16974693,"end":16975013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112414.14","gene_symbol":"ADGRG6","gene_name":"adhesion G protein-coupled receptor G6 [Source:HGNC Symbol;Acc:HGNC:13841]","synonyms":"GPR126,FLJ14937","biotype":"protein_coding","ncbi_id":"57211","summary":"This gene, which is upregulated in human umbilical vein endothelial cells, encodes a G protein-coupled receptor. Variations in this gene can affect a person's stature. Multiple transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Mar 2009]","start":142301854,"end":142446266,"strand":1,"description":"adhesion G protein-coupled receptor G6 [Source:HGNC Symbol;Acc:HGNC:13841]"}, {"versioned_ensembl_gene_id":"ENSG00000073282.12","gene_symbol":"TP63","gene_name":"tumor protein p63 [Source:HGNC Symbol;Acc:HGNC:15979]","synonyms":"p63,p53CP,p51,OFC8,NBP,KET,EEC3,TP73L,TP53L,TP53CP,SHFM4,p73L,p73H","biotype":"protein_coding","ncbi_id":"8626","summary":"This gene encodes a member of the p53 family of transcription factors. The functional domains of p53 family proteins include an N-terminal transactivation domain, a central DNA-binding domain and an oligomerization domain. Alternative splicing of this gene and the use of alternative promoters results in multiple transcript variants encoding different isoforms that vary in their functional properties. These isoforms function during skin development and maintenance, adult stem/progenitor cell regulation, heart development and premature aging. Some isoforms have been found to protect the germline by eliminating oocytes or testicular germ cells that have suffered DNA damage. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. [provided by RefSeq, Aug 2016]","start":189631416,"end":189897279,"strand":1,"description":"tumor protein p63 [Source:HGNC Symbol;Acc:HGNC:15979]"}, {"versioned_ensembl_gene_id":"ENSG00000267927.1","gene_symbol":"AC010320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52171158,"end":52177002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270252.1","gene_symbol":"IGKV3OR2-5","gene_name":"immunoglobulin kappa variable 3/OR2-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5832]","synonyms":"IGKV3/OR2-5","biotype":"IG_V_pseudogene","ncbi_id":"28854","summary":null,"start":97348899,"end":97349179,"strand":1,"description":"immunoglobulin kappa variable 3/OR2-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5832]"}, {"versioned_ensembl_gene_id":"ENSG00000213253.5","gene_symbol":"RPL12P42","gene_name":"ribosomal protein L12 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129394","summary":null,"start":13157959,"end":13158788,"strand":-1,"description":"ribosomal protein L12 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36165]"}, {"versioned_ensembl_gene_id":"ENSG00000228990.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969980,"end":28971310,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000281012.1","gene_symbol":"AC116165.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23196959,"end":23197164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131037.14","gene_symbol":"EPS8L1","gene_name":"EPS8 like 1 [Source:HGNC Symbol;Acc:HGNC:21295]","synonyms":"MGC4642,MGC23164,FLJ20258,DRC3","biotype":"protein_coding","ncbi_id":"54869","summary":"This gene encodes a protein that is related to epidermal growth factor receptor pathway substrate 8 (EPS8), a substrate for the epidermal growth factor receptor. The function of this protein is unknown. At least two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":55072020,"end":55087923,"strand":1,"description":"EPS8 like 1 [Source:HGNC Symbol;Acc:HGNC:21295]"}, {"versioned_ensembl_gene_id":"ENSG00000273080.1","gene_symbol":"AC009309.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86195590,"end":86196049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255009.4","gene_symbol":"UBTFL1","gene_name":"upstream binding transcription factor, RNA polymerase I-like 1 [Source:HGNC Symbol;Acc:HGNC:14533]","synonyms":"C11orf27","biotype":"protein_coding","ncbi_id":"642623","summary":"UBTFL1 is a preimplantation-specific gene and is involved in early development, implantation, and embryonic stem (ES) cell derivation (summary by Yamada et al., 2010 [PubMed 19915186]).[supplied by OMIM, Jan 2011]","start":90085950,"end":90087131,"strand":1,"description":"upstream binding transcription factor, RNA polymerase I-like 1 [Source:HGNC Symbol;Acc:HGNC:14533]"}, {"versioned_ensembl_gene_id":"ENSG00000181751.9","gene_symbol":"C5orf30","gene_name":"chromosome 5 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:25052]","synonyms":"FLJ25291","biotype":"protein_coding","ncbi_id":"90355","summary":"This gene, MACIR (previously known as C5orf30), has been associated with rheumatoid arthritis, functioning as a negative regulator of tissue damage and modulating the activity of synovial fibroblasts and macrophages. The encoded protein is highly conserved in vertebrate genomes but has no significant similarity to any other human protein. [provided by RefSeq, Dec 2019]","start":103258702,"end":103278660,"strand":1,"description":"chromosome 5 open reading frame 30 [Source:HGNC Symbol;Acc:HGNC:25052]"}, {"versioned_ensembl_gene_id":"ENSG00000197093.10","gene_symbol":"GAL3ST4","gene_name":"galactose-3-O-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:24145]","synonyms":"FLJ12116","biotype":"protein_coding","ncbi_id":"79690","summary":"This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate to the C-3' position of galactose residues in O-linked glycoproteins. This enzyme is highly specific for core 1 structures, with asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc being good substrates. [provided by RefSeq, Jul 2008]","start":100159244,"end":100168750,"strand":-1,"description":"galactose-3-O-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:24145]"}, {"versioned_ensembl_gene_id":"ENSG00000108255.7","gene_symbol":"CRYBA1","gene_name":"crystallin beta A1 [Source:HGNC Symbol;Acc:HGNC:2394]","synonyms":"CRYB1","biotype":"protein_coding","ncbi_id":"1411","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta acidic group member, encodes two proteins (crystallin, beta A3 and crystallin, beta A1) from a single mRNA, the latter protein is 17 aa shorter than crystallin, beta A3 and is generated by use of an alternate translation initiation site. Deletion of exons 3 and 4 causes the autosomal dominant disease 'zonular cataract with sutural opacities'. [provided by RefSeq, Jul 2008]","start":29246863,"end":29254494,"strand":1,"description":"crystallin beta A1 [Source:HGNC Symbol;Acc:HGNC:2394]"}, {"versioned_ensembl_gene_id":"ENSG00000128918.14","gene_symbol":"ALDH1A2","gene_name":"aldehyde dehydrogenase 1 family member A2 [Source:HGNC Symbol;Acc:HGNC:15472]","synonyms":"RALDH2","biotype":"protein_coding","ncbi_id":"8854","summary":"This protein belongs to the aldehyde dehydrogenase family of proteins. The product of this gene is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde. Retinoic acid, the active derivative of vitamin A (retinol), is a hormonal signaling molecule that functions in developing and adult tissues. The studies of a similar mouse gene suggest that this enzyme and the cytochrome CYP26A1, concurrently establish local embryonic retinoic acid levels which facilitate posterior organ development and prevent spina bifida. Four transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, May 2011]","start":57953424,"end":58497866,"strand":-1,"description":"aldehyde dehydrogenase 1 family member A2 [Source:HGNC Symbol;Acc:HGNC:15472]"}, {"versioned_ensembl_gene_id":"ENSG00000274719.1","gene_symbol":"AC012653.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":57990217,"end":57990636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168129.8","gene_symbol":"DHFRP3","gene_name":"dihydrofolate reductase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52354]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1720","summary":null,"start":82856826,"end":82857384,"strand":1,"description":"dihydrofolate reductase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52354]"}, {"versioned_ensembl_gene_id":"ENSG00000266869.1","gene_symbol":"AC005993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71848606,"end":71908430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225486.1","gene_symbol":"AL663058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":233836080,"end":233836432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271299.1","gene_symbol":"AC008962.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41073804,"end":41074107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283828.1","gene_symbol":"AL137002.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113149432,"end":113154002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153044.9","gene_symbol":"CENPH","gene_name":"centromere protein H [Source:HGNC Symbol;Acc:HGNC:17268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64946","summary":"Centromere and kinetochore proteins play a critical role in centromere structure, kinetochore formation, and sister chromatid separation. The protein encoded by this gene colocalizes with inner kinetochore plate proteins CENP-A and CENP-C in both interphase and metaphase. It localizes outside of centromeric heterochromatin, where CENP-B is localized, and inside the kinetochore corona, where CENP-E is localized during prometaphase. It is thought that this protein can bind to itself, as well as to CENP-A, CENP-B or CENP-C. Multimers of the protein localize constitutively to the inner kinetochore plate and play an important role in the organization and function of the active centromere-kinetochore complex. [provided by RefSeq, Jul 2008]","start":69189548,"end":69210357,"strand":1,"description":"centromere protein H [Source:HGNC Symbol;Acc:HGNC:17268]"}, {"versioned_ensembl_gene_id":"ENSG00000181135.15","gene_symbol":"ZNF707","gene_name":"zinc finger protein 707 [Source:HGNC Symbol;Acc:HGNC:27815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286075","summary":null,"start":143684452,"end":143713898,"strand":1,"description":"zinc finger protein 707 [Source:HGNC Symbol;Acc:HGNC:27815]"}, {"versioned_ensembl_gene_id":"ENSG00000231882.1","gene_symbol":"F10-AS1","gene_name":"F10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40225]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104413892","summary":null,"start":113128155,"end":113128880,"strand":-1,"description":"F10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40225]"}, {"versioned_ensembl_gene_id":"ENSG00000117475.13","gene_symbol":"BLZF1","gene_name":"basic leucine zipper nuclear factor 1 [Source:HGNC Symbol;Acc:HGNC:1065]","synonyms":"JEM-1","biotype":"protein_coding","ncbi_id":"8548","summary":null,"start":169367970,"end":169396540,"strand":1,"description":"basic leucine zipper nuclear factor 1 [Source:HGNC Symbol;Acc:HGNC:1065]"}, {"versioned_ensembl_gene_id":"ENSG00000104450.12","gene_symbol":"SPAG1","gene_name":"sperm associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:11212]","synonyms":"TPIS,SP75,HSD-3.8,FLJ32920,CT140,CILD28","biotype":"protein_coding","ncbi_id":"6674","summary":"The correlation of anti-sperm antibodies with cases of unexplained infertility implicates a role for these antibodies in blocking fertilization. Improved diagnosis and treatment of immunologic infertility, as well as identification of proteins for targeted contraception, are dependent on the identification and characterization of relevant sperm antigens. The protein expressed by this gene is recognized by anti-sperm agglutinating antibodies from an infertile woman. Furthermore, immunization of female rats with the recombinant human protein reduced fertility. This protein localizes to the plasma membrane of germ cells in the testis and to the post-acrosomal plasma membrane of mature spermatozoa. Recombinant polypeptide binds GTP and exhibits GTPase activity. Thus, this protein may regulate GTP signal transduction pathways involved in spermatogenesis and fertilization. Two transcript variants of this gene encode the same protein. [provided by RefSeq, Jul 2008]","start":100157906,"end":100259278,"strand":1,"description":"sperm associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:11212]"}, {"versioned_ensembl_gene_id":"ENSG00000162396.5","gene_symbol":"PARS2","gene_name":"prolyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:30563]","synonyms":"DKFZp727A071","biotype":"protein_coding","ncbi_id":"25973","summary":"This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of proline to tRNA molecules. Mutations have been found in this gene in some patients with Alpers syndrome. [provided by RefSeq, Mar 2015]","start":54756898,"end":54764514,"strand":-1,"description":"prolyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:30563]"}, {"versioned_ensembl_gene_id":"ENSG00000272874.1","gene_symbol":"AL034548.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":267186,"end":268857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213145.9","gene_symbol":"CRIP1","gene_name":"cysteine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2360]","synonyms":"CRIP","biotype":"protein_coding","ncbi_id":"1396","summary":"Cysteine-rich intestinal protein (CRIP) belongs to the LIM/double zinc finger protein family, members of which include cysteine- and glycine-rich protein-1 (CSRP1; MIM 123876), rhombotin-1 (RBTN1; MIM 186921), rhombotin-2 (RBTN2; MIM 180385), and rhombotin-3 (RBTN3; MIM 180386). CRIP may be involved in intestinal zinc transport (Hempe and Cousins, 1991 [PubMed 1946385]).[supplied by OMIM, Mar 2008]","start":105486317,"end":105488947,"strand":1,"description":"cysteine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:2360]"}, {"versioned_ensembl_gene_id":"ENSG00000119608.12","gene_symbol":"PROX2","gene_name":"prospero homeobox 2 [Source:HGNC Symbol;Acc:HGNC:26715]","synonyms":"FLJ36749","biotype":"protein_coding","ncbi_id":"283571","summary":null,"start":74852871,"end":74871940,"strand":-1,"description":"prospero homeobox 2 [Source:HGNC Symbol;Acc:HGNC:26715]"}, {"versioned_ensembl_gene_id":"ENSG00000186458.4","gene_symbol":"DEFB132","gene_name":"defensin beta 132 [Source:HGNC Symbol;Acc:HGNC:33806]","synonyms":"RP5-1103G7.6,DEFB32","biotype":"protein_coding","ncbi_id":"400830","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The protein encoded by this gene is secreted and is a member of the beta defensin protein family. This protein binds spermatozoa and has antimicrobial activity against E. coli. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":257736,"end":261096,"strand":1,"description":"defensin beta 132 [Source:HGNC Symbol;Acc:HGNC:33806]"}, {"versioned_ensembl_gene_id":"ENSG00000125903.4","gene_symbol":"DEFB129","gene_name":"defensin beta 129 [Source:HGNC Symbol;Acc:HGNC:16218]","synonyms":"DEFB-29,C20orf87,bA530N10.3","biotype":"protein_coding","ncbi_id":"140881","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":227258,"end":229886,"strand":1,"description":"defensin beta 129 [Source:HGNC Symbol;Acc:HGNC:16218]"}, {"versioned_ensembl_gene_id":"ENSG00000173908.8","gene_symbol":"KRT28","gene_name":"keratin 28 [Source:HGNC Symbol;Acc:HGNC:30842]","synonyms":"KRT25D","biotype":"protein_coding","ncbi_id":"162605","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40792203,"end":40799959,"strand":-1,"description":"keratin 28 [Source:HGNC Symbol;Acc:HGNC:30842]"}, {"versioned_ensembl_gene_id":"ENSG00000221874.4","gene_symbol":"ZNF816-ZNF321P","gene_name":"ZNF816-ZNF321P readthrough [Source:HGNC Symbol;Acc:HGNC:38879]","synonyms":"ZNF816-ZNF321","biotype":"protein_coding","ncbi_id":"100529240","summary":"This locus represents naturally occurring read-through transcription between the zinc finger protein 816 (ZNF816) gene and the zinc finger protein 321 (ZNF321) pseudogene on chromosome 19. The read-through transcript encodes a KRAB domain-containing protein that shares sequence identity with the upstream gene product, but it contains a distinct C-terminus encoded by exon structure from the downstream pseudogene. [provided by RefSeq, Jan 2011]","start":52928475,"end":52962823,"strand":-1,"description":"ZNF816-ZNF321P readthrough [Source:HGNC Symbol;Acc:HGNC:38879]"}, {"versioned_ensembl_gene_id":"ENSG00000104883.7","gene_symbol":"PEX11G","gene_name":"peroxisomal biogenesis factor 11 gamma [Source:HGNC Symbol;Acc:HGNC:20208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92960","summary":"The protein encoded by this gene is a member of the PEX11 family. This family is reported to regulate the number and size of peroxisomes in evolutionarily distant organisms. The protein encoded by this gene may induce clustering of peroxisomes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":7476875,"end":7497449,"strand":-1,"description":"peroxisomal biogenesis factor 11 gamma [Source:HGNC Symbol;Acc:HGNC:20208]"}, {"versioned_ensembl_gene_id":"ENSG00000186143.11","gene_symbol":"PRR30","gene_name":"proline rich 30 [Source:HGNC Symbol;Acc:HGNC:28677]","synonyms":"MGC44505,C2orf53","biotype":"protein_coding","ncbi_id":"339779","summary":null,"start":27136848,"end":27139410,"strand":-1,"description":"proline rich 30 [Source:HGNC Symbol;Acc:HGNC:28677]"}, {"versioned_ensembl_gene_id":"ENSG00000230987.2","gene_symbol":"AL359976.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189989570,"end":189993097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139318.7","gene_symbol":"DUSP6","gene_name":"dual specificity phosphatase 6 [Source:HGNC Symbol;Acc:HGNC:3072]","synonyms":"PYST1,MKP-3","biotype":"protein_coding","ncbi_id":"1848","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates ERK2, is expressed in a variety of tissues with the highest levels in heart and pancreas, and unlike most other members of this family, is localized in the cytoplasm. Mutations in this gene have been associated with congenital hypogonadotropic hypogonadism. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014]","start":89347232,"end":89353271,"strand":-1,"description":"dual specificity phosphatase 6 [Source:HGNC Symbol;Acc:HGNC:3072]"}, {"versioned_ensembl_gene_id":"ENSG00000186393.5","gene_symbol":"KRT26","gene_name":"keratin 26 [Source:HGNC Symbol;Acc:HGNC:30840]","synonyms":"KRT25B","biotype":"protein_coding","ncbi_id":"353288","summary":"The protein encoded by this gene is a member of the keratin superfamily. This keratin protein is a type I keratin that is specific for the inner root sheath of the hair follicle. This gene exists in a cluster with other keratin genes on chromosome 17q21. [provided by RefSeq, Jul 2009]","start":40766238,"end":40772162,"strand":-1,"description":"keratin 26 [Source:HGNC Symbol;Acc:HGNC:30840]"}, {"versioned_ensembl_gene_id":"ENSG00000233325.3","gene_symbol":"MIPEPP3","gene_name":"mitochondrial intermediate peptidase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39458]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"650794","summary":null,"start":21298139,"end":21306373,"strand":1,"description":"mitochondrial intermediate peptidase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39458]"}, {"versioned_ensembl_gene_id":"ENSG00000232085.1","gene_symbol":"AL606534.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":243164638,"end":243169445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265692.1","gene_symbol":"LINC01970","gene_name":"long intergenic non-protein coding RNA 1970 [Source:HGNC Symbol;Acc:HGNC:52796]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929511","summary":null,"start":82290046,"end":82292814,"strand":-1,"description":"long intergenic non-protein coding RNA 1970 [Source:HGNC Symbol;Acc:HGNC:52796]"}, {"versioned_ensembl_gene_id":"ENSG00000249255.1","gene_symbol":"PGAM1P9","gene_name":"phosphoglycerate mutase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420681","summary":null,"start":92366496,"end":92367250,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42456]"}, {"versioned_ensembl_gene_id":"ENSG00000240125.1","gene_symbol":"RPL23AP75","gene_name":"ribosomal protein L23a pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:35975]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728207","summary":null,"start":40439467,"end":40439917,"strand":-1,"description":"ribosomal protein L23a pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:35975]"}, {"versioned_ensembl_gene_id":"ENSG00000225581.3","gene_symbol":"TRIM53AP","gene_name":"tripartite motif containing 53A, pseudogene [Source:HGNC Symbol;Acc:HGNC:19025]","synonyms":"TRIM53P,TRIM53","biotype":"unprocessed_pseudogene","ncbi_id":"642569","summary":null,"start":89993536,"end":89999741,"strand":-1,"description":"tripartite motif containing 53A, pseudogene [Source:HGNC Symbol;Acc:HGNC:19025]"}, {"versioned_ensembl_gene_id":"ENSG00000239407.5","gene_symbol":"Z68871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102884414,"end":102906158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229794.2","gene_symbol":"MTCYBP32","gene_name":"mitochondrially encoded cytochrome b pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52174]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075231","summary":null,"start":102806741,"end":102807824,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52174]"}, {"versioned_ensembl_gene_id":"ENSG00000282810.1","gene_symbol":"MIR210HG","gene_name":"MIR210 host gene [Source:HGNC Symbol;Acc:HGNC:39524]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506211","summary":null,"start":565674,"end":568471,"strand":-1,"description":"MIR210 host gene [Source:HGNC Symbol;Acc:HGNC:39524]"}, {"versioned_ensembl_gene_id":"ENSG00000271985.1","gene_symbol":"BX248123.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79526508,"end":79526631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144460.12","gene_symbol":"NYAP2","gene_name":"neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2 [Source:HGNC Symbol;Acc:HGNC:29291]","synonyms":"KIAA1486","biotype":"protein_coding","ncbi_id":"57624","summary":null,"start":225399710,"end":225654018,"strand":1,"description":"neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2 [Source:HGNC Symbol;Acc:HGNC:29291]"}, {"versioned_ensembl_gene_id":"ENSG00000235705.5","gene_symbol":"AL133481.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":79507597,"end":79510922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283255.1","gene_symbol":"AL022100.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168401483,"end":168407274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228697.2","gene_symbol":"AL023755.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168400829,"end":168495685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235470.5","gene_symbol":"NEURL1-AS1","gene_name":"NEURL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51220]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724341","summary":null,"start":103479603,"end":103517393,"strand":-1,"description":"NEURL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51220]"}, {"versioned_ensembl_gene_id":"ENSG00000176155.18","gene_symbol":"CCDC57","gene_name":"coiled-coil domain containing 57 [Source:HGNC Symbol;Acc:HGNC:27564]","synonyms":"FLJ23754,FLJ00130","biotype":"protein_coding","ncbi_id":"284001","summary":null,"start":82101460,"end":82212830,"strand":-1,"description":"coiled-coil domain containing 57 [Source:HGNC Symbol;Acc:HGNC:27564]"}, {"versioned_ensembl_gene_id":"ENSG00000178222.12","gene_symbol":"RNF212","gene_name":"ring finger protein 212 [Source:HGNC Symbol;Acc:HGNC:27729]","synonyms":"LOC285498,FLJ38841","biotype":"protein_coding","ncbi_id":"285498","summary":"This gene encodes a RING finger protein that may function as a ubiquitin ligase. The encoded protein may be involved in meiotic recombination. This gene is located within a linkage disequilibrium block and polymorphisms in this gene may influence recombination rates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]","start":1056250,"end":1113562,"strand":-1,"description":"ring finger protein 212 [Source:HGNC Symbol;Acc:HGNC:27729]"}, {"versioned_ensembl_gene_id":"ENSG00000143367.15","gene_symbol":"TUFT1","gene_name":"tuftelin 1 [Source:HGNC Symbol;Acc:HGNC:12422]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7286","summary":"Tuftelin is an acidic protein that is thought to play a role in dental enamel mineralization and is implicated in caries susceptibility. It is also thought to be involved with adaptation to hypoxia, mesenchymal stem cell function, and neurotrophin nerve growth factor mediated neuronal differentiation. [provided by RefSeq, Aug 2014]","start":151540305,"end":151583583,"strand":1,"description":"tuftelin 1 [Source:HGNC Symbol;Acc:HGNC:12422]"}, {"versioned_ensembl_gene_id":"ENSG00000023330.14","gene_symbol":"ALAS1","gene_name":"5'-aminolevulinate synthase 1 [Source:HGNC Symbol;Acc:HGNC:396]","synonyms":"ALAS3,ALAS","biotype":"protein_coding","ncbi_id":"211","summary":"This gene encodes the mitochondrial enzyme which is catalyzes the rate-limiting step in heme (iron-protoporphyrin) biosynthesis. The enzyme encoded by this gene is the housekeeping enzyme; a separate gene encodes a form of the enzyme that is specific for erythroid tissue. The level of the mature encoded protein is regulated by heme: high levels of heme down-regulate the mature enzyme in mitochondria while low heme levels up-regulate. A pseudogene of this gene is located on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2015]","start":52198086,"end":52214327,"strand":1,"description":"5'-aminolevulinate synthase 1 [Source:HGNC Symbol;Acc:HGNC:396]"}, {"versioned_ensembl_gene_id":"ENSG00000197475.11","gene_symbol":"ADAM3A","gene_name":"ADAM metallopeptidase domain 3A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:209]","synonyms":"tMDCI,CYRN1,ADAM3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"1587","summary":null,"start":39451045,"end":39522852,"strand":-1,"description":"ADAM metallopeptidase domain 3A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:209]"}, {"versioned_ensembl_gene_id":"ENSG00000173954.8","gene_symbol":"SNURFL","gene_name":"SNRPN upstream reading frame-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:29543]","synonyms":"CXorf19","biotype":"processed_pseudogene","ncbi_id":"727686","summary":null,"start":139362040,"end":139362382,"strand":1,"description":"SNRPN upstream reading frame-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:29543]"}, {"versioned_ensembl_gene_id":"ENSG00000274276.4","gene_symbol":"CBSL","gene_name":"cystathionine-beta-synthase like [Source:HGNC Symbol;Acc:HGNC:51829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724560","summary":null,"start":6444869,"end":6468040,"strand":-1,"description":"cystathionine-beta-synthase like [Source:HGNC Symbol;Acc:HGNC:51829]"}, {"versioned_ensembl_gene_id":"ENSG00000266117.1","gene_symbol":"FBXO36P1","gene_name":"F-box protein 36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"732538","summary":null,"start":68095068,"end":68095757,"strand":1,"description":"F-box protein 36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50363]"}, {"versioned_ensembl_gene_id":"ENSG00000255300.5","gene_symbol":"AC079917.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41993385,"end":42163851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108468.14","gene_symbol":"CBX1","gene_name":"chromobox 1 [Source:HGNC Symbol;Acc:HGNC:1551]","synonyms":"MOD1,M31,HP1Hs-beta,HP1-BETA,CBX","biotype":"protein_coding","ncbi_id":"10951","summary":"This gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family . The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N-terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C-terminal chromo shadow-domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin-associated nonhistone proteins. The protein may play an important role in the epigenetic control of chromatin structure and gene expression. Several related pseudogenes are located on chromosomes 1, 3, and X. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":48070052,"end":48101521,"strand":-1,"description":"chromobox 1 [Source:HGNC Symbol;Acc:HGNC:1551]"}, {"versioned_ensembl_gene_id":"ENSG00000027644.4","gene_symbol":"INSRR","gene_name":"insulin receptor related receptor [Source:HGNC Symbol;Acc:HGNC:6093]","synonyms":"IRR","biotype":"protein_coding","ncbi_id":"3645","summary":null,"start":156840063,"end":156859018,"strand":-1,"description":"insulin receptor related receptor [Source:HGNC Symbol;Acc:HGNC:6093]"}, {"versioned_ensembl_gene_id":"ENSG00000224551.1","gene_symbol":"HMGB3P21","gene_name":"high mobility group box 3 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39313]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873901","summary":null,"start":97135015,"end":97135561,"strand":-1,"description":"high mobility group box 3 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39313]"}, {"versioned_ensembl_gene_id":"ENSG00000276778.1","gene_symbol":"LINC02227","gene_name":"long intergenic non-protein coding RNA 2227 [Source:HGNC Symbol;Acc:HGNC:53096]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927697","summary":null,"start":158320683,"end":158409773,"strand":-1,"description":"long intergenic non-protein coding RNA 2227 [Source:HGNC Symbol;Acc:HGNC:53096]"}, {"versioned_ensembl_gene_id":"ENSG00000083290.19","gene_symbol":"ULK2","gene_name":"unc-51 like autophagy activating kinase 2 [Source:HGNC Symbol;Acc:HGNC:13480]","synonyms":"Unc51.2,KIAA0623,ATG1B","biotype":"protein_coding","ncbi_id":"9706","summary":"This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]","start":19770829,"end":19867936,"strand":-1,"description":"unc-51 like autophagy activating kinase 2 [Source:HGNC Symbol;Acc:HGNC:13480]"}, {"versioned_ensembl_gene_id":"ENSG00000270681.1","gene_symbol":"AC095055.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151139991,"end":151141103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212855.5","gene_symbol":"TTTY2","gene_name":"testis-specific transcript, Y-linked 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14023]","synonyms":"TTY2,lINC00109","biotype":"lincRNA","ncbi_id":"60439","summary":null,"start":9740584,"end":9758476,"strand":1,"description":"testis-specific transcript, Y-linked 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14023]"}, {"versioned_ensembl_gene_id":"ENSG00000108370.16","gene_symbol":"RGS9","gene_name":"regulator of G protein signaling 9 [Source:HGNC Symbol;Acc:HGNC:10004]","synonyms":"RGS9L,PERRS,MGC26458,MGC111763","biotype":"protein_coding","ncbi_id":"8787","summary":"This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":65100812,"end":65227703,"strand":1,"description":"regulator of G protein signaling 9 [Source:HGNC Symbol;Acc:HGNC:10004]"}, {"versioned_ensembl_gene_id":"ENSG00000261167.1","gene_symbol":"AC107027.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":131455126,"end":131458598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269927.1","gene_symbol":"AC004817.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71141125,"end":71143253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169750.8","gene_symbol":"RAC3","gene_name":"ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3) [Source:HGNC Symbol;Acc:HGNC:9803]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5881","summary":"The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":82031624,"end":82034204,"strand":1,"description":"ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3) [Source:HGNC Symbol;Acc:HGNC:9803]"}, {"versioned_ensembl_gene_id":"ENSG00000214930.2","gene_symbol":"KRT8P6","gene_name":"keratin 8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392552","summary":null,"start":138487665,"end":138488871,"strand":-1,"description":"keratin 8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33360]"}, {"versioned_ensembl_gene_id":"ENSG00000254492.1","gene_symbol":"AP001328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102154550,"end":102154725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258509.1","gene_symbol":"AL049870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44887434,"end":44887741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211862.1","gene_symbol":"TRAJ27","gene_name":"T-cell receptor alpha joining 27 [Source:HGNC Symbol;Acc:HGNC:12056]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28728","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22516273,"end":22516331,"strand":1,"description":"T-cell receptor alpha joining 27 [Source:HGNC Symbol;Acc:HGNC:12056]"}, {"versioned_ensembl_gene_id":"ENSG00000254971.1","gene_symbol":"AP003122.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89753982,"end":89754953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255170.2","gene_symbol":"AP003122.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89764884,"end":89765138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277099.1","gene_symbol":"BX571673.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":242060490,"end":242062595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254822.1","gene_symbol":"AC023442.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41876634,"end":41877078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155833.14","gene_symbol":"CYLC2","gene_name":"cylicin 2 [Source:HGNC Symbol;Acc:HGNC:2583]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1539","summary":"Cylicin II (CYCL2) is specifically expressed in testis and is part of the cytoskeletal calyx of mammalian sperm heads. Cylicin II may play a role in the morphogenesis of the sperm head. [provided by RefSeq, Jul 2008]","start":102995311,"end":103018488,"strand":1,"description":"cylicin 2 [Source:HGNC Symbol;Acc:HGNC:2583]"}, {"versioned_ensembl_gene_id":"ENSG00000129911.8","gene_symbol":"KLF16","gene_name":"Kruppel like factor 16 [Source:HGNC Symbol;Acc:HGNC:16857]","synonyms":"NSLP2,DRRF,BTEB4","biotype":"protein_coding","ncbi_id":"83855","summary":null,"start":1852399,"end":1863568,"strand":-1,"description":"Kruppel like factor 16 [Source:HGNC Symbol;Acc:HGNC:16857]"}, {"versioned_ensembl_gene_id":"ENSG00000125691.12","gene_symbol":"RPL23","gene_name":"ribosomal protein L23 [Source:HGNC Symbol;Acc:HGNC:10316]","synonyms":"rpL17,L23","biotype":"protein_coding","ncbi_id":"9349","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L14P family of ribosomal proteins. It is located in the cytoplasm. This gene has been referred to as rpL17 because the encoded protein shares amino acid identity with ribosomal protein L17 from Saccharomyces cerevisiae; however, its official symbol is RPL23. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":38847865,"end":38853843,"strand":-1,"description":"ribosomal protein L23 [Source:HGNC Symbol;Acc:HGNC:10316]"}, {"versioned_ensembl_gene_id":"ENSG00000260769.1","gene_symbol":"AC007614.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49337167,"end":49338993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242461.1","gene_symbol":"AC089999.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113054062,"end":113054435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166266.13","gene_symbol":"CUL5","gene_name":"cullin 5 [Source:HGNC Symbol;Acc:HGNC:2556]","synonyms":"VACM-1","biotype":"protein_coding","ncbi_id":"8065","summary":null,"start":108008733,"end":108107776,"strand":1,"description":"cullin 5 [Source:HGNC Symbol;Acc:HGNC:2556]"}, {"versioned_ensembl_gene_id":"ENSG00000211860.1","gene_symbol":"TRAJ29","gene_name":"T-cell receptor alpha joining 29 [Source:HGNC Symbol;Acc:HGNC:12058]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28726","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22513939,"end":22513998,"strand":1,"description":"T-cell receptor alpha joining 29 [Source:HGNC Symbol;Acc:HGNC:12058]"}, {"versioned_ensembl_gene_id":"ENSG00000226991.2","gene_symbol":"AC140479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110358790,"end":110359126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243695.1","gene_symbol":"AL353729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39173794,"end":39174513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213177.3","gene_symbol":"PRDX2P4","gene_name":"peroxiredoxin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442239","summary":null,"start":100136064,"end":100136663,"strand":1,"description":"peroxiredoxin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44969]"}, {"versioned_ensembl_gene_id":"ENSG00000254946.1","gene_symbol":"AC073172.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15552855,"end":15591098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104835.14","gene_symbol":"SARS2","gene_name":"seryl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17697]","synonyms":"FLJ20450,SYS,SERS,SerRSmt,SARSM,SARS,mtSerRS","biotype":"protein_coding","ncbi_id":"54938","summary":"This gene encodes the mitochondrial seryl-tRNA synthethase precursor, a member of the class II tRNA synthetase family. The mature enzyme catalyzes the ligation of Serine to tRNA(Ser) and participates in the biosynthesis of selenocysteinyl-tRNA(sec) in mitochondria. The enzyme contains an N-terminal tRNA binding domain and a core catalytic domain. It functions in a homodimeric form, which is stabilized by tRNA binding. This gene is regulated by a bidirectional promoter that also controls the expression of mitochondrial ribosomal protein S12. Both genes are within the critical interval for the autosomal dominant deafness locus DFNA4 and might be linked to this disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Mar 2009]","start":38915266,"end":38930896,"strand":-1,"description":"seryl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17697]"}, {"versioned_ensembl_gene_id":"ENSG00000251492.1","gene_symbol":"AC104136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136004509,"end":136004902,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234883.5","gene_symbol":"MIR155HG","gene_name":"MIR155 host gene [Source:HGNC Symbol;Acc:HGNC:35460]","synonyms":"NCRNA00172,MIRHG2,BIC","biotype":"lincRNA","ncbi_id":"114614","summary":"This gene represents a microRNA host gene. The long RNA transcribed from this gene is expressed at high levels in lymphoma and may function as an oncogene. [provided by RefSeq, Dec 2017]","start":25561909,"end":25575168,"strand":1,"description":"MIR155 host gene [Source:HGNC Symbol;Acc:HGNC:35460]"}, {"versioned_ensembl_gene_id":"ENSG00000232480.1","gene_symbol":"TGFB2-AS1","gene_name":"TGFB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50628]","synonyms":"NR_046268","biotype":"antisense_RNA","ncbi_id":"728463","summary":null,"start":218344196,"end":218345678,"strand":-1,"description":"TGFB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50628]"}, {"versioned_ensembl_gene_id":"ENSG00000258859.1","gene_symbol":"LINC02296","gene_name":"long intergenic non-protein coding RNA 2296 [Source:HGNC Symbol;Acc:HGNC:53212]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370610","summary":null,"start":87353070,"end":87573022,"strand":-1,"description":"long intergenic non-protein coding RNA 2296 [Source:HGNC Symbol;Acc:HGNC:53212]"}, {"versioned_ensembl_gene_id":"ENSG00000237555.1","gene_symbol":"AL031681.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43388642,"end":43389041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282005.1","gene_symbol":"AC138374.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":557613,"end":560121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165832.5","gene_symbol":"TRUB1","gene_name":"TruB pseudouridine synthase family member 1 [Source:HGNC Symbol;Acc:HGNC:16060]","synonyms":"PUS4","biotype":"protein_coding","ncbi_id":"142940","summary":"Pseudouridine is an abundant component of rRNAs and tRNAs and is enzymatically generated by isomerization of uridine by pseudouridine synthase (Zucchini et al., 2003 [PubMed 12736709]).[supplied by OMIM, Mar 2008]","start":114938193,"end":114977676,"strand":1,"description":"TruB pseudouridine synthase family member 1 [Source:HGNC Symbol;Acc:HGNC:16060]"}, {"versioned_ensembl_gene_id":"ENSG00000256292.1","gene_symbol":"LINC02376","gene_name":"long intergenic non-protein coding RNA 2376 [Source:HGNC Symbol;Acc:HGNC:53298]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370065","summary":null,"start":127274467,"end":127284283,"strand":-1,"description":"long intergenic non-protein coding RNA 2376 [Source:HGNC Symbol;Acc:HGNC:53298]"}, {"versioned_ensembl_gene_id":"ENSG00000254812.1","gene_symbol":"AC067930.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143632071,"end":143633756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272589.1","gene_symbol":"ZSWIM8-AS1","gene_name":"ZSWIM8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45103]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507331","summary":null,"start":73796514,"end":73801399,"strand":-1,"description":"ZSWIM8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45103]"}, {"versioned_ensembl_gene_id":"ENSG00000254930.1","gene_symbol":"LINC02545","gene_name":"long intergenic non-protein coding RNA 2545 [Source:HGNC Symbol;Acc:HGNC:53580]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376561","summary":null,"start":13844862,"end":13870616,"strand":-1,"description":"long intergenic non-protein coding RNA 2545 [Source:HGNC Symbol;Acc:HGNC:53580]"}, {"versioned_ensembl_gene_id":"ENSG00000232080.5","gene_symbol":"AL662789.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32718005,"end":32719170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224769.1","gene_symbol":"MUC20P1","gene_name":"mucin 20, cell surface associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51921]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"651714","summary":null,"start":195614947,"end":195620233,"strand":1,"description":"mucin 20, cell surface associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51921]"}, {"versioned_ensembl_gene_id":"ENSG00000277136.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41442102,"end":41442392,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000211845.1","gene_symbol":"TRAJ44","gene_name":"T-cell receptor alpha joining 44 [Source:HGNC Symbol;Acc:HGNC:12075]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28711","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22494821,"end":22494883,"strand":1,"description":"T-cell receptor alpha joining 44 [Source:HGNC Symbol;Acc:HGNC:12075]"}, {"versioned_ensembl_gene_id":"ENSG00000261226.1","gene_symbol":"AC092384.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":88936779,"end":88939651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066336.11","gene_symbol":"SPI1","gene_name":"Spi-1 proto-oncogene [Source:HGNC Symbol;Acc:HGNC:11241]","synonyms":"SFPI1,PU.1,OF,SPI-A,SPI-1","biotype":"protein_coding","ncbi_id":"6688","summary":"This gene encodes an ETS-domain transcription factor that activates gene expression during myeloid and B-lymphoid cell development. The nuclear protein binds to a purine-rich sequence known as the PU-box found near the promoters of target genes, and regulates their expression in coordination with other transcription factors and cofactors. The protein can also regulate alternative splicing of target genes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47354860,"end":47378576,"strand":-1,"description":"Spi-1 proto-oncogene [Source:HGNC Symbol;Acc:HGNC:11241]"}, {"versioned_ensembl_gene_id":"ENSG00000213333.3","gene_symbol":"NPM1P50","gene_name":"nucleophosmin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45229]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100129795","summary":null,"start":75079265,"end":75080131,"strand":-1,"description":"nucleophosmin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45229]"}, {"versioned_ensembl_gene_id":"ENSG00000228816.1","gene_symbol":"AK3P5","gene_name":"adenylate kinase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39064]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288319","summary":null,"start":32944481,"end":32944999,"strand":1,"description":"adenylate kinase 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39064]"}, {"versioned_ensembl_gene_id":"ENSG00000214796.8","gene_symbol":"AC098934.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":202851828,"end":202861620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132386.10","gene_symbol":"SERPINF1","gene_name":"serpin family F member 1 [Source:HGNC Symbol;Acc:HGNC:8824]","synonyms":"PIG35,PEDF,EPC-1","biotype":"protein_coding","ncbi_id":"5176","summary":"This gene encodes a member of the serpin family that does not display the serine protease inhibitory activity shown by many of the other serpin proteins. The encoded protein is secreted and strongly inhibits angiogenesis. In addition, this protein is a neurotrophic factor involved in neuronal differentiation in retinoblastoma cells. Mutations in this gene were found in individuals with osteogenesis imperfecta, type VI. [provided by RefSeq, Aug 2016]","start":1761959,"end":1777574,"strand":1,"description":"serpin family F member 1 [Source:HGNC Symbol;Acc:HGNC:8824]"}, {"versioned_ensembl_gene_id":"ENSG00000198758.10","gene_symbol":"EPS8L3","gene_name":"EPS8 like 3 [Source:HGNC Symbol;Acc:HGNC:21297]","synonyms":"FLJ21522,MGC16817","biotype":"protein_coding","ncbi_id":"79574","summary":"This gene encodes a protein that is related to epidermal growth factor receptor pathway substrate 8 (EPS8), a substrate for the epidermal growth factor receptor. The function of this protein is unknown. Alternatively spliced transcript variants encoding different isoforms exist. [provided by RefSeq, Jul 2008]","start":109750080,"end":109764027,"strand":-1,"description":"EPS8 like 3 [Source:HGNC Symbol;Acc:HGNC:21297]"}, {"versioned_ensembl_gene_id":"ENSG00000134201.10","gene_symbol":"GSTM5","gene_name":"glutathione S-transferase mu 5 [Source:HGNC Symbol;Acc:HGNC:4637]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2949","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. [provided by RefSeq, Jul 2008]","start":109712255,"end":109775428,"strand":1,"description":"glutathione S-transferase mu 5 [Source:HGNC Symbol;Acc:HGNC:4637]"}, {"versioned_ensembl_gene_id":"ENSG00000228484.1","gene_symbol":"AL137025.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114764788,"end":114779903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258753.1","gene_symbol":"AL359792.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54470709,"end":54471218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248323.5","gene_symbol":"LUCAT1","gene_name":"lung cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48498]","synonyms":"SCAL1","biotype":"lincRNA","ncbi_id":"100505994","summary":null,"start":91303029,"end":91314402,"strand":-1,"description":"lung cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48498]"}, {"versioned_ensembl_gene_id":"ENSG00000258600.1","gene_symbol":"AL359238.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83017106,"end":83018144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258683.1","gene_symbol":"AL355095.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82788478,"end":82796221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282236.1","gene_symbol":"TRBV5-2","gene_name":"T-cell receptor beta variable 5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12219]","synonyms":"TRBV52,TCRBV5S2P,TCRBV31S1","biotype":"TR_V_pseudogene","ncbi_id":"28613","summary":null,"start":142394342,"end":142394614,"strand":1,"description":"T-cell receptor beta variable 5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12219]"}, {"versioned_ensembl_gene_id":"ENSG00000236704.1","gene_symbol":"CNOT4P1","gene_name":"CCR4-NOT transcription complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39272]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874389","summary":null,"start":20921664,"end":20923233,"strand":-1,"description":"CCR4-NOT transcription complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39272]"}, {"versioned_ensembl_gene_id":"ENSG00000229820.2","gene_symbol":"CR391992.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28453541,"end":28453934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230549.3","gene_symbol":"USP17L1","gene_name":"ubiquitin specific peptidase 17-like family member 1 [Source:HGNC Symbol;Acc:HGNC:37182]","synonyms":"USP17L1P","biotype":"protein_coding","ncbi_id":"401447","summary":null,"start":7332387,"end":7333979,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 1 [Source:HGNC Symbol;Acc:HGNC:37182]"}, {"versioned_ensembl_gene_id":"ENSG00000217094.2","gene_symbol":"PPIAP31","gene_name":"peptidylprolyl isomerase A pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:44962]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"439953","summary":null,"start":32188323,"end":32188817,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:44962]"}, {"versioned_ensembl_gene_id":"ENSG00000227354.6","gene_symbol":"RBM26-AS1","gene_name":"RBM26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39805]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505538","summary":null,"start":79406309,"end":79424328,"strand":1,"description":"RBM26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39805]"}, {"versioned_ensembl_gene_id":"ENSG00000236632.5","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30534109,"end":30538847,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000234269.2","gene_symbol":"AL365396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102922574,"end":102923244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214869.5","gene_symbol":"TPM3P4","gene_name":"tropomyosin 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402643","summary":null,"start":27023737,"end":27024907,"strand":1,"description":"tropomyosin 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39167]"}, {"versioned_ensembl_gene_id":"ENSG00000255279.1","gene_symbol":"AC023442.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41855920,"end":41875997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182179.12","gene_symbol":"UBA7","gene_name":"ubiquitin like modifier activating enzyme 7 [Source:HGNC Symbol;Acc:HGNC:12471]","synonyms":"UBE2,UBE1L,UBA1B,D8","biotype":"protein_coding","ncbi_id":"7318","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E1 ubiquitin-activating enzyme family. The encoded enzyme is a retinoid target that triggers promyelocytic leukemia (PML)/retinoic acid receptor alpha (RARalpha) degradation and apoptosis in acute promyelocytic leukemia, where it is involved in the conjugation of the ubiquitin-like interferon-stimulated gene 15 protein. [provided by RefSeq, Jul 2008]","start":49805207,"end":49813946,"strand":-1,"description":"ubiquitin like modifier activating enzyme 7 [Source:HGNC Symbol;Acc:HGNC:12471]"}, {"versioned_ensembl_gene_id":"ENSG00000172680.1","gene_symbol":"MOS","gene_name":"MOS proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:7199]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4342","summary":"MOS is a serine/threonine kinase that activates the MAP kinase cascade through direct phosphorylation of the MAP kinase activator MEK (MAP2K1; MIM 176872) (Prasad et al., 2008 [PubMed 18246541]).[supplied by OMIM, Jul 2009]","start":56112942,"end":56113982,"strand":-1,"description":"MOS proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:7199]"}, {"versioned_ensembl_gene_id":"ENSG00000260815.3","gene_symbol":"AC019294.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75746769,"end":75747263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246877.1","gene_symbol":"DNM1P35","gene_name":"dynamin 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35182]","synonyms":"DNM1DN8@,DNM1DN8-2","biotype":"antisense_RNA","ncbi_id":"100128285","summary":null,"start":75727670,"end":75738623,"strand":-1,"description":"dynamin 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35182]"}, {"versioned_ensembl_gene_id":"ENSG00000100814.17","gene_symbol":"CCNB1IP1","gene_name":"cyclin B1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:19437]","synonyms":"HEI10,C14orf18","biotype":"protein_coding","ncbi_id":"57820","summary":"HEI10 is a member of the E3 ubiquitin ligase family and functions in progression of the cell cycle through G(2)/M.[supplied by OMIM, Apr 2004]","start":20311368,"end":20333312,"strand":-1,"description":"cyclin B1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:19437]"}, {"versioned_ensembl_gene_id":"ENSG00000204977.9","gene_symbol":"TRIM13","gene_name":"tripartite motif containing 13 [Source:HGNC Symbol;Acc:HGNC:9976]","synonyms":"RNF77,RFP2,Leu5,DLEU5","biotype":"protein_coding","ncbi_id":"10206","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This gene is located on chromosome 13 within the minimal deletion region for B-cell chronic lymphocytic leukemia. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":49995888,"end":50020481,"strand":1,"description":"tripartite motif containing 13 [Source:HGNC Symbol;Acc:HGNC:9976]"}, {"versioned_ensembl_gene_id":"ENSG00000228728.1","gene_symbol":"AF274573.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150818753,"end":150819246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118363.11","gene_symbol":"SPCS2","gene_name":"signal peptidase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28962]","synonyms":"KIAA0102","biotype":"protein_coding","ncbi_id":"9789","summary":null,"start":74949247,"end":74979031,"strand":1,"description":"signal peptidase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28962]"}, {"versioned_ensembl_gene_id":"ENSG00000254811.5","gene_symbol":"AP002001.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106250019,"end":106264905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258499.1","gene_symbol":"LINC02287","gene_name":"long intergenic non-protein coding RNA 2287 [Source:HGNC Symbol;Acc:HGNC:53204]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929002","summary":null,"start":92905697,"end":92907482,"strand":-1,"description":"long intergenic non-protein coding RNA 2287 [Source:HGNC Symbol;Acc:HGNC:53204]"}, {"versioned_ensembl_gene_id":"ENSG00000260436.1","gene_symbol":"AC093525.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2571570,"end":2572353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146205.13","gene_symbol":"ANO7","gene_name":"anoctamin 7 [Source:HGNC Symbol;Acc:HGNC:31677]","synonyms":"TMEM16G,PCANAP5L,PCANAP5,NGEP,IPCA-5","biotype":"protein_coding","ncbi_id":"50636","summary":"This prostate-specific gene encodes a cytoplasmic protein, as well as a polytopic membrane protein which may serve as a target in prostate cancer diagnosis and immunotherapy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2011]","start":241188509,"end":241225377,"strand":1,"description":"anoctamin 7 [Source:HGNC Symbol;Acc:HGNC:31677]"}, {"versioned_ensembl_gene_id":"ENSG00000182256.12","gene_symbol":"GABRG3","gene_name":"gamma-aminobutyric acid type A receptor gamma3 subunit [Source:HGNC Symbol;Acc:HGNC:4088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2567","summary":"This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. The protein encoded by this gene is a gamma subunit, which contains the benzodiazepine binding site. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2012]","start":26971282,"end":27541991,"strand":1,"description":"gamma-aminobutyric acid type A receptor gamma3 subunit [Source:HGNC Symbol;Acc:HGNC:4088]"}, {"versioned_ensembl_gene_id":"ENSG00000224686.1","gene_symbol":"ELOCP23","gene_name":"elongin C pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:38159]","synonyms":"TCEB1P23","biotype":"processed_pseudogene","ncbi_id":"100462881","summary":null,"start":78488182,"end":78488513,"strand":1,"description":"elongin C pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:38159]"}, {"versioned_ensembl_gene_id":"ENSG00000225462.1","gene_symbol":"FDPSP1","gene_name":"farnesyl diphosphate synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3632]","synonyms":"FPSL1,FDPSL1,CHR39A","biotype":"processed_pseudogene","ncbi_id":"343332","summary":null,"start":187563061,"end":187564131,"strand":1,"description":"farnesyl diphosphate synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3632]"}, {"versioned_ensembl_gene_id":"ENSG00000230937.11","gene_symbol":"MIR205HG","gene_name":"MIR205 host gene [Source:HGNC Symbol;Acc:HGNC:43562]","synonyms":"LINC00510","biotype":"processed_transcript","ncbi_id":"642587","summary":null,"start":209428820,"end":209432838,"strand":1,"description":"MIR205 host gene [Source:HGNC Symbol;Acc:HGNC:43562]"}, {"versioned_ensembl_gene_id":"ENSG00000232237.3","gene_symbol":"ASCL5","gene_name":"achaete-scute family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:33169]","synonyms":"bHLHa47","biotype":"protein_coding","ncbi_id":"647219","summary":null,"start":201113953,"end":201127184,"strand":-1,"description":"achaete-scute family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:33169]"}, {"versioned_ensembl_gene_id":"ENSG00000180458.2","gene_symbol":"AC022148.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37545470,"end":37549171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107819.13","gene_symbol":"SFXN3","gene_name":"sideroflexin 3 [Source:HGNC Symbol;Acc:HGNC:16087]","synonyms":"SFX3","biotype":"protein_coding","ncbi_id":"81855","summary":null,"start":101031234,"end":101041244,"strand":1,"description":"sideroflexin 3 [Source:HGNC Symbol;Acc:HGNC:16087]"}, {"versioned_ensembl_gene_id":"ENSG00000183432.6","gene_symbol":"ZBTB8OSP1","gene_name":"zinc finger and BTB domain containing 8 opposite strand pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729566","summary":null,"start":150720981,"end":150721478,"strand":1,"description":"zinc finger and BTB domain containing 8 opposite strand pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19043]"}, {"versioned_ensembl_gene_id":"ENSG00000273984.4","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195745705,"end":195790439,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000242034.1","gene_symbol":"AC097493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9553614,"end":9553985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249443.1","gene_symbol":"AC097493.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9521910,"end":9522276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253994.1","gene_symbol":"NDUFB9P3","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52271]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129370","summary":null,"start":110809394,"end":110809894,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52271]"}, {"versioned_ensembl_gene_id":"ENSG00000263382.1","gene_symbol":"AC018371.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26822813,"end":26823979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229229.1","gene_symbol":"AC022201.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70402934,"end":70422678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166211.7","gene_symbol":"SPIC","gene_name":"Spi-C transcription factor [Source:HGNC Symbol;Acc:HGNC:29549]","synonyms":"SPI-C,MGC40611","biotype":"protein_coding","ncbi_id":"121599","summary":"The protein encoded by this gene regulates the development of red pulp macrophages, which are necessary for iron homeostasis and the recycling of red blood cells. [provided by RefSeq, Aug 2016]","start":101475421,"end":101486997,"strand":1,"description":"Spi-C transcription factor [Source:HGNC Symbol;Acc:HGNC:29549]"}, {"versioned_ensembl_gene_id":"ENSG00000213822.6","gene_symbol":"AC020914.1","gene_name":"Carcinoembryonic antigen-related cell adhesion molecule 18 [Source:UniProtKB/Swiss-Prot;Acc:A8MTB9]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":51478622,"end":51490952,"strand":1,"description":"Carcinoembryonic antigen-related cell adhesion molecule 18 [Source:UniProtKB/Swiss-Prot;Acc:A8MTB9]"}, {"versioned_ensembl_gene_id":"ENSG00000182796.13","gene_symbol":"TMEM198B","gene_name":"transmembrane protein 198B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43629]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"440104","summary":null,"start":55829608,"end":55836246,"strand":1,"description":"transmembrane protein 198B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43629]"}, {"versioned_ensembl_gene_id":"ENSG00000226903.1","gene_symbol":"LINC00354","gene_name":"long intergenic non-protein coding RNA 354 [Source:HGNC Symbol;Acc:HGNC:42672]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928616","summary":null,"start":111899985,"end":111901176,"strand":1,"description":"long intergenic non-protein coding RNA 354 [Source:HGNC Symbol;Acc:HGNC:42672]"}, {"versioned_ensembl_gene_id":"ENSG00000277258.4","gene_symbol":"PCGF2","gene_name":"polycomb group ring finger 2 [Source:HGNC Symbol;Acc:HGNC:12929]","synonyms":"ZNF144,RNF110,MEL-18","biotype":"protein_coding","ncbi_id":"7703","summary":"The protein encoded by this gene contains a RING finger motif and is similar to the polycomb group (PcG) gene products. PcG gene products form complexes via protein-protein interaction and maintain the transcription repression of genes involved in embryogenesis, cell cycles, and tumorigenesis. This protein was shown to act as a negative regulator of transcription and has tumor suppressor activity. The expression of this gene was detected in various tumor cells, but is limited in neural organs in normal tissues. Knockout studies in mice suggested that this protein may negatively regulate the expression of different cytokines, chemokines, and chemokine receptors, and thus plays an important role in lymphocyte differentiation and migration, as well as in immune responses. [provided by RefSeq, Jul 2008]","start":38733897,"end":38749817,"strand":-1,"description":"polycomb group ring finger 2 [Source:HGNC Symbol;Acc:HGNC:12929]"}, {"versioned_ensembl_gene_id":"ENSG00000218049.1","gene_symbol":"AL591034.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53368670,"end":53369009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256963.1","gene_symbol":"AC079602.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121079842,"end":121080124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270336.1","gene_symbol":"AC105148.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167741879,"end":167742287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086991.12","gene_symbol":"NOX4","gene_name":"NADPH oxidase 4 [Source:HGNC Symbol;Acc:HGNC:7891]","synonyms":"KOX-1,KOX","biotype":"protein_coding","ncbi_id":"50507","summary":"This gene encodes a member of the NOX-family of enzymes that functions as the catalytic subunit the NADPH oxidase complex. The encoded protein is localized to non-phagocytic cells where it acts as an oxygen sensor and catalyzes the reduction of molecular oxygen to various reactive oxygen species (ROS). The ROS generated by this protein have been implicated in numerous biological functions including signal transduction, cell differentiation and tumor cell growth. A pseudogene has been identified on the other arm of chromosome 11. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2009]","start":89324356,"end":89498187,"strand":-1,"description":"NADPH oxidase 4 [Source:HGNC Symbol;Acc:HGNC:7891]"}, {"versioned_ensembl_gene_id":"ENSG00000250150.1","gene_symbol":"AC079349.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167306910,"end":167308789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271353.1","gene_symbol":"AC012468.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119562101,"end":119562530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183186.7","gene_symbol":"C2CD4C","gene_name":"C2 calcium dependent domain containing 4C [Source:HGNC Symbol;Acc:HGNC:29417]","synonyms":"NLF3,KIAA1957,FAM148C","biotype":"protein_coding","ncbi_id":"126567","summary":null,"start":405438,"end":409170,"strand":-1,"description":"C2 calcium dependent domain containing 4C [Source:HGNC Symbol;Acc:HGNC:29417]"}, {"versioned_ensembl_gene_id":"ENSG00000120688.8","gene_symbol":"WBP4","gene_name":"WW domain binding protein 4 [Source:HGNC Symbol;Acc:HGNC:12739]","synonyms":"MGC117310,FBP21","biotype":"protein_coding","ncbi_id":"11193","summary":"This gene encodes WW domain-containing binding protein 4. The WW domain represents a small and compact globular structure that interacts with proline-rich ligands. This encoded protein is a general spliceosomal protein that may play a role in cross-intron bridging of U1 and U2 snRNPs in the spliceosomal complex A. [provided by RefSeq, Jul 2008]","start":41061274,"end":41084006,"strand":1,"description":"WW domain binding protein 4 [Source:HGNC Symbol;Acc:HGNC:12739]"}, {"versioned_ensembl_gene_id":"ENSG00000121989.14","gene_symbol":"ACVR2A","gene_name":"activin A receptor type 2A [Source:HGNC Symbol;Acc:HGNC:173]","synonyms":"ACVR2,ACTRII","biotype":"protein_coding","ncbi_id":"92","summary":"This gene encodes a receptor that mediates the functions of activins, which are members of the transforming growth factor-beta (TGF-beta) superfamily involved in diverse biological processes. The encoded protein is a transmembrane serine-threonine kinase receptor which mediates signaling by forming heterodimeric complexes with various combinations of type I and type II receptors and ligands in a cell-specific manner. The encoded type II receptor is primarily involved in ligand-binding and includes an extracellular ligand-binding domain, a transmembrane domain and a cytoplasmic serine-threonine kinase domain. This gene may be associated with susceptibility to preeclampsia, a pregnancy-related disease which can result in maternal and fetal morbidity and mortality. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jun 2013]","start":147844517,"end":147930826,"strand":1,"description":"activin A receptor type 2A [Source:HGNC Symbol;Acc:HGNC:173]"}, {"versioned_ensembl_gene_id":"ENSG00000106400.11","gene_symbol":"ZNHIT1","gene_name":"zinc finger HIT-type containing 1 [Source:HGNC Symbol;Acc:HGNC:21688]","synonyms":"ZNFN4A1,H_DJ0747G18.14,CG1I","biotype":"protein_coding","ncbi_id":"10467","summary":null,"start":101217668,"end":101224190,"strand":1,"description":"zinc finger HIT-type containing 1 [Source:HGNC Symbol;Acc:HGNC:21688]"}, {"versioned_ensembl_gene_id":"ENSG00000120690.15","gene_symbol":"ELF1","gene_name":"E74 like ETS transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3316]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1997","summary":"This gene encodes an E26 transformation-specific related transcription factor. The encoded protein is primarily expressed in lymphoid cells and acts as both an enhancer and a repressor to regulate transcription of various genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009]","start":40932028,"end":41061440,"strand":-1,"description":"E74 like ETS transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3316]"}, {"versioned_ensembl_gene_id":"ENSG00000197866.3","gene_symbol":"OR5M12P","gene_name":"olfactory receptor family 5 subfamily M member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15292]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81188","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56628932,"end":56629860,"strand":1,"description":"olfactory receptor family 5 subfamily M member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15292]"}, {"versioned_ensembl_gene_id":"ENSG00000242163.1","gene_symbol":"AL121769.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81332961,"end":81333361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161999.11","gene_symbol":"JMJD8","gene_name":"jumonji domain containing 8 [Source:HGNC Symbol;Acc:HGNC:14148]","synonyms":"C16orf20","biotype":"protein_coding","ncbi_id":"339123","summary":null,"start":681671,"end":684528,"strand":-1,"description":"jumonji domain containing 8 [Source:HGNC Symbol;Acc:HGNC:14148]"}, {"versioned_ensembl_gene_id":"ENSG00000229469.2","gene_symbol":"CR788300.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29574010,"end":29574937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239524.2","gene_symbol":"RPL32P34","gene_name":"ribosomal protein L32 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35903]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133162","summary":null,"start":5277734,"end":5278133,"strand":1,"description":"ribosomal protein L32 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35903]"}, {"versioned_ensembl_gene_id":"ENSG00000141030.12","gene_symbol":"COPS3","gene_name":"COP9 signalosome subunit 3 [Source:HGNC Symbol;Acc:HGNC:2239]","synonyms":"SGN3,CSN3","biotype":"protein_coding","ncbi_id":"8533","summary":"The protein encoded by this gene possesses kinase activity that phosphorylates regulators involved in signal transduction. It phosphorylates I kappa-Balpha, p105, and c-Jun. It acts as a docking site for complex-mediated phosphorylation. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":17246820,"end":17281293,"strand":-1,"description":"COP9 signalosome subunit 3 [Source:HGNC Symbol;Acc:HGNC:2239]"}, {"versioned_ensembl_gene_id":"ENSG00000233370.1","gene_symbol":"AC140479.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110184054,"end":110185179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256458.1","gene_symbol":"AC080075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203328459,"end":203329226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140995.16","gene_symbol":"DEF8","gene_name":"differentially expressed in FDCP 8 homolog [Source:HGNC Symbol;Acc:HGNC:25969]","synonyms":"FLJ20186","biotype":"protein_coding","ncbi_id":"54849","summary":null,"start":89947925,"end":89968060,"strand":1,"description":"differentially expressed in FDCP 8 homolog [Source:HGNC Symbol;Acc:HGNC:25969]"}, {"versioned_ensembl_gene_id":"ENSG00000160229.11","gene_symbol":"ZNF66","gene_name":"zinc finger protein 66 [Source:HGNC Symbol;Acc:HGNC:13135]","synonyms":"ZNF66P,FLJ16537","biotype":"protein_coding","ncbi_id":"7617","summary":null,"start":20776304,"end":20807322,"strand":1,"description":"zinc finger protein 66 [Source:HGNC Symbol;Acc:HGNC:13135]"}, {"versioned_ensembl_gene_id":"ENSG00000134184.12","gene_symbol":"GSTM1","gene_name":"glutathione S-transferase mu 1 [Source:HGNC Symbol;Acc:HGNC:4632]","synonyms":"MU,H-B,GST1","biotype":"protein_coding","ncbi_id":"2944","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Null mutations of this class mu gene have been linked with an increase in a number of cancers, likely due to an increased susceptibility to environmental toxins and carcinogens. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":109687814,"end":109709039,"strand":1,"description":"glutathione S-transferase mu 1 [Source:HGNC Symbol;Acc:HGNC:4632]"}, {"versioned_ensembl_gene_id":"ENSG00000035141.7","gene_symbol":"FAM136A","gene_name":"family with sequence similarity 136 member A [Source:HGNC Symbol;Acc:HGNC:25911]","synonyms":"FLJ14668","biotype":"protein_coding","ncbi_id":"84908","summary":"This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":70295975,"end":70302090,"strand":-1,"description":"family with sequence similarity 136 member A [Source:HGNC Symbol;Acc:HGNC:25911]"}, {"versioned_ensembl_gene_id":"ENSG00000279434.1","gene_symbol":"AL049776.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35086035,"end":35088059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282683.1","gene_symbol":"AC236721.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143065916,"end":143066603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273198.1","gene_symbol":"AL096803.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186521773,"end":186522304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251306.1","gene_symbol":"NDUFB4P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45250]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132036","summary":null,"start":59528861,"end":59529251,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45250]"}, {"versioned_ensembl_gene_id":"ENSG00000166693.7","gene_symbol":"OR5M13P","gene_name":"olfactory receptor family 5 subfamily M member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15293]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81187","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56597426,"end":56598362,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15293]"}, {"versioned_ensembl_gene_id":"ENSG00000183808.11","gene_symbol":"RBM12B","gene_name":"RNA binding motif protein 12B [Source:HGNC Symbol;Acc:HGNC:32310]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389677","summary":null,"start":93729356,"end":93741017,"strand":-1,"description":"RNA binding motif protein 12B [Source:HGNC Symbol;Acc:HGNC:32310]"}, {"versioned_ensembl_gene_id":"ENSG00000271971.1","gene_symbol":"AC120053.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93715378,"end":93716113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166548.15","gene_symbol":"TK2","gene_name":"thymidine kinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:11831]","synonyms":"SCA31","biotype":"protein_coding","ncbi_id":"7084","summary":"This gene encodes a deoxyribonucleoside kinase that specifically phosphorylates thymidine, deoxycytidine, and deoxyuridine. The encoded enzyme localizes to the mitochondria and is required for mitochondrial DNA synthesis. Mutations in this gene are associated with a myopathic form of mitochondrial DNA depletion syndrome. Alternate splicing results in multiple transcript variants encoding distinct isoforms, some of which lack transit peptide, so are not localized to mitochondria. [provided by RefSeq, Dec 2012]","start":66508003,"end":66552544,"strand":-1,"description":"thymidine kinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:11831]"}, {"versioned_ensembl_gene_id":"ENSG00000273783.1","gene_symbol":"AL136040.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81221218,"end":81222460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265218.1","gene_symbol":"AC103810.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64892729,"end":64910180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163558.12","gene_symbol":"PRKCI","gene_name":"protein kinase C iota [Source:HGNC Symbol;Acc:HGNC:9404]","synonyms":"PKCI,DXS1179E","biotype":"protein_coding","ncbi_id":"5584","summary":"This gene encodes a member of the protein kinase C (PKC) family of serine/threonine protein kinases. The PKC family comprises at least eight members, which are differentially expressed and are involved in a wide variety of cellular processes. This protein kinase is calcium-independent and phospholipid-dependent. It is not activated by phorbolesters or diacylglycerol. This kinase can be recruited to vesicle tubular clusters (VTCs) by direct interaction with the small GTPase RAB2, where this kinase phosphorylates glyceraldehyde-3-phosphate dehydrogenase (GAPD/GAPDH) and plays a role in microtubule dynamics in the early secretory pathway. This kinase is found to be necessary for BCL-ABL-mediated resistance to drug-induced apoptosis and therefore protects leukemia cells against drug-induced apoptosis. There is a single exon pseudogene mapped on chromosome X. [provided by RefSeq, Jul 2008]","start":170222365,"end":170305981,"strand":1,"description":"protein kinase C iota [Source:HGNC Symbol;Acc:HGNC:9404]"}, {"versioned_ensembl_gene_id":"ENSG00000255863.2","gene_symbol":"AC073610.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":48921963,"end":48939663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203914.4","gene_symbol":"HSP90B3P","gene_name":"heat shock protein 90 beta family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:12100]","synonyms":"TRAP2,TRA1P2,GRP94c","biotype":"processed_pseudogene","ncbi_id":"343477","summary":null,"start":91642516,"end":91644082,"strand":1,"description":"heat shock protein 90 beta family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:12100]"}, {"versioned_ensembl_gene_id":"ENSG00000203879.11","gene_symbol":"GDI1","gene_name":"GDP dissociation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:4226]","synonyms":"XAP-4,RABGDIA,OPHN2,MRX48,MRX41,GDIL,FLJ41411","biotype":"protein_coding","ncbi_id":"2664","summary":"GDP dissociation inhibitors are proteins that regulate the GDP-GTP exchange reaction of members of the rab family, small GTP-binding proteins of the ras superfamily, that are involved in vesicular trafficking of molecules between cellular organelles. GDIs slow the rate of dissociation of GDP from rab proteins and release GDP from membrane-bound rabs. GDI1 is expressed primarily in neural and sensory tissues. Mutations in GDI1 have been linked to X-linked nonspecific cognitive disability. [provided by RefSeq, Jul 2008]","start":154436913,"end":154443467,"strand":1,"description":"GDP dissociation inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:4226]"}, {"versioned_ensembl_gene_id":"ENSG00000135338.13","gene_symbol":"LCA5","gene_name":"LCA5, lebercilin [Source:HGNC Symbol;Acc:HGNC:31923]","synonyms":"C6orf152","biotype":"protein_coding","ncbi_id":"167691","summary":"This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]","start":79484991,"end":79537458,"strand":-1,"description":"LCA5, lebercilin [Source:HGNC Symbol;Acc:HGNC:31923]"}, {"versioned_ensembl_gene_id":"ENSG00000249680.2","gene_symbol":"TUBA3GP","gene_name":"tubulin alpha 3g pseudogene [Source:HGNC Symbol;Acc:HGNC:44096]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645348","summary":null,"start":21065462,"end":21070097,"strand":1,"description":"tubulin alpha 3g pseudogene [Source:HGNC Symbol;Acc:HGNC:44096]"}, {"versioned_ensembl_gene_id":"ENSG00000248375.1","gene_symbol":"AC104066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52720081,"end":52720831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000019144.18","gene_symbol":"PHLDB1","gene_name":"pleckstrin homology like domain family B member 1 [Source:HGNC Symbol;Acc:HGNC:23697]","synonyms":"LL5a,KIAA0638,FLJ00141","biotype":"protein_coding","ncbi_id":"23187","summary":null,"start":118606440,"end":118658038,"strand":1,"description":"pleckstrin homology like domain family B member 1 [Source:HGNC Symbol;Acc:HGNC:23697]"}, {"versioned_ensembl_gene_id":"ENSG00000224595.1","gene_symbol":"AC073626.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114414244,"end":114419875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229544.8","gene_symbol":"NKX1-2","gene_name":"NK1 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:31652]","synonyms":"C10orf121,bB238F13.2","biotype":"protein_coding","ncbi_id":"390010","summary":null,"start":124445239,"end":124450184,"strand":-1,"description":"NK1 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:31652]"}, {"versioned_ensembl_gene_id":"ENSG00000271184.1","gene_symbol":"AC005252.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125900421,"end":125901483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168939.11","gene_symbol":"SPRY3","gene_name":"sprouty RTK signaling antagonist 3 [Source:HGNC Symbol;Acc:HGNC:11271]","synonyms":"HSPRY3","biotype":"protein_coding","ncbi_id":"10251","summary":null,"start":155767812,"end":155782459,"strand":1,"description":"sprouty RTK signaling antagonist 3 [Source:HGNC Symbol;Acc:HGNC:11271]"}, {"versioned_ensembl_gene_id":"ENSG00000229042.2","gene_symbol":"AL031656.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42685404,"end":42688562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204694.11","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425504,"end":29457071,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000172489.6","gene_symbol":"OR5T3","gene_name":"olfactory receptor family 5 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:15297]","synonyms":"OR5T3Q","biotype":"protein_coding","ncbi_id":"390154","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56252200,"end":56253222,"strand":1,"description":"olfactory receptor family 5 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:15297]"}, {"versioned_ensembl_gene_id":"ENSG00000236292.1","gene_symbol":"AC138024.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216194051,"end":216204366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283597.2","gene_symbol":"FAM169B","gene_name":"family with sequence similarity 169 member B [Source:HGNC Symbol;Acc:HGNC:26835]","synonyms":"KIAA0888L,FLJ39743","biotype":"protein_coding","ncbi_id":"283777","summary":null,"start":98437162,"end":98547728,"strand":-1,"description":"family with sequence similarity 169 member B [Source:HGNC Symbol;Acc:HGNC:26835]"}, {"versioned_ensembl_gene_id":"ENSG00000108733.9","gene_symbol":"PEX12","gene_name":"peroxisomal biogenesis factor 12 [Source:HGNC Symbol;Acc:HGNC:8854]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5193","summary":"This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]","start":35574795,"end":35578863,"strand":-1,"description":"peroxisomal biogenesis factor 12 [Source:HGNC Symbol;Acc:HGNC:8854]"}, {"versioned_ensembl_gene_id":"ENSG00000179460.5","gene_symbol":"EEF1A1P27","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37900]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130234","summary":null,"start":20582072,"end":20583206,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37900]"}, {"versioned_ensembl_gene_id":"ENSG00000126243.8","gene_symbol":"LRFN3","gene_name":"leucine rich repeat and fibronectin type III domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28370]","synonyms":"FIGLER1,SALM4,MGC2656","biotype":"protein_coding","ncbi_id":"79414","summary":null,"start":35935358,"end":35945767,"strand":1,"description":"leucine rich repeat and fibronectin type III domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28370]"}, {"versioned_ensembl_gene_id":"ENSG00000236579.2","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"HCGIX-4,PERB11,HCGIX,HCGIX4","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29964608,"end":29967904,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000258731.1","gene_symbol":"AL356020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53153354,"end":53157528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262180.1","gene_symbol":"OCLM","gene_name":"oculomedin [Source:HGNC Symbol;Acc:HGNC:8103]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10896","summary":null,"start":186400572,"end":186401455,"strand":1,"description":"oculomedin [Source:HGNC Symbol;Acc:HGNC:8103]"}, {"versioned_ensembl_gene_id":"ENSG00000112651.11","gene_symbol":"MRPL2","gene_name":"mitochondrial ribosomal protein L2 [Source:HGNC Symbol;Acc:HGNC:14056]","synonyms":"RPML14,MRP-L14,CGI-22","biotype":"protein_coding","ncbi_id":"51069","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the EcoL2 ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 12q. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":43054029,"end":43059806,"strand":-1,"description":"mitochondrial ribosomal protein L2 [Source:HGNC Symbol;Acc:HGNC:14056]"}, {"versioned_ensembl_gene_id":"ENSG00000197782.14","gene_symbol":"ZNF780A","gene_name":"zinc finger protein 780A [Source:HGNC Symbol;Acc:HGNC:27603]","synonyms":"ZNF780","biotype":"protein_coding","ncbi_id":"284323","summary":null,"start":40069152,"end":40090938,"strand":-1,"description":"zinc finger protein 780A [Source:HGNC Symbol;Acc:HGNC:27603]"}, {"versioned_ensembl_gene_id":"ENSG00000205923.3","gene_symbol":"CEMP1","gene_name":"cementum protein 1 [Source:HGNC Symbol;Acc:HGNC:32553]","synonyms":"CP-23","biotype":"protein_coding","ncbi_id":"752014","summary":null,"start":2530035,"end":2531417,"strand":-1,"description":"cementum protein 1 [Source:HGNC Symbol;Acc:HGNC:32553]"}, {"versioned_ensembl_gene_id":"ENSG00000258416.1","gene_symbol":"AF123462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79893080,"end":79974169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226872.1","gene_symbol":"AC002472.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21031357,"end":21043969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233462.4","gene_symbol":"AL671561.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29796886,"end":29797682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270504.1","gene_symbol":"AL391422.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3751111,"end":3753871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118922.17","gene_symbol":"KLF12","gene_name":"Kruppel like factor 12 [Source:HGNC Symbol;Acc:HGNC:6346]","synonyms":"HSPC122,AP2REP,AP-2rep","biotype":"protein_coding","ncbi_id":"11278","summary":"Activator protein-2 alpha (AP-2 alpha) is a developmentally-regulated transcription factor and important regulator of gene expression during vertebrate development and carcinogenesis. The protein encoded by this gene is a member of the Kruppel-like zinc finger protein family and can repress expression of the AP-2 alpha gene by binding to a specific site in the AP-2 alpha gene promoter. Repression by the encoded protein requires binding with a corepressor, CtBP1. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":73686089,"end":73995056,"strand":-1,"description":"Kruppel like factor 12 [Source:HGNC Symbol;Acc:HGNC:6346]"}, {"versioned_ensembl_gene_id":"ENSG00000237493.3","gene_symbol":"AC034102.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55980432,"end":55981035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179304.16","gene_symbol":"FAM156B","gene_name":"family with sequence similarity 156 member B [Source:HGNC Symbol;Acc:HGNC:31962]","synonyms":"TMEM29B","biotype":"protein_coding","ncbi_id":"727866","summary":null,"start":52891306,"end":52908560,"strand":1,"description":"family with sequence similarity 156 member B [Source:HGNC Symbol;Acc:HGNC:31962]"}, {"versioned_ensembl_gene_id":"ENSG00000104823.8","gene_symbol":"ECH1","gene_name":"enoyl-CoA hydratase 1 [Source:HGNC Symbol;Acc:HGNC:3149]","synonyms":"HPXEL","biotype":"protein_coding","ncbi_id":"1891","summary":"This gene encodes a member of the hydratase/isomerase superfamily. The gene product shows high sequence similarity to enoyl-coenzyme A (CoA) hydratases of several species, particularly within a conserved domain characteristic of these proteins. The encoded protein, which contains a C-terminal peroxisomal targeting sequence, localizes to the peroxisome. The rat ortholog, which localizes to the matrix of both the peroxisome and mitochondria, can isomerize 3-trans,5-cis-dienoyl-CoA to 2-trans,4-trans-dienoyl-CoA, indicating that it is a delta3,5-delta2,4-dienoyl-CoA isomerase. This enzyme functions in the auxiliary step of the fatty acid beta-oxidation pathway. Expression of the rat gene is induced by peroxisome proliferators. [provided by RefSeq, Jul 2008]","start":38815422,"end":38832005,"strand":-1,"description":"enoyl-CoA hydratase 1 [Source:HGNC Symbol;Acc:HGNC:3149]"}, {"versioned_ensembl_gene_id":"ENSG00000231002.7","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30229518,"end":30258487,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000260179.1","gene_symbol":"AL162741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1249777,"end":1251334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235066.6","gene_symbol":"AC009303.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117995397,"end":118055033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235712.10","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"NR2B2,H-2RIIBP,RCoR-1","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33363951,"end":33371048,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000226404.9","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31658863,"end":31666220,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000161992.5","gene_symbol":"PRR35","gene_name":"proline rich 35 [Source:HGNC Symbol;Acc:HGNC:14139]","synonyms":"C16orf11","biotype":"protein_coding","ncbi_id":"146325","summary":null,"start":560422,"end":565528,"strand":1,"description":"proline rich 35 [Source:HGNC Symbol;Acc:HGNC:14139]"}, {"versioned_ensembl_gene_id":"ENSG00000217527.1","gene_symbol":"RPS16P5","gene_name":"ribosomal protein S16 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36183]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"647190","summary":null,"start":53336943,"end":53337346,"strand":-1,"description":"ribosomal protein S16 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36183]"}, {"versioned_ensembl_gene_id":"ENSG00000155816.19","gene_symbol":"FMN2","gene_name":"formin 2 [Source:HGNC Symbol;Acc:HGNC:14074]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56776","summary":"This gene is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. This protein mediates the formation of an actin mesh that positions the spindle during oogenesis and also regulates the formation of actin filaments in the nucleus. This protein also forms a perinuclear actin/focal-adhesion system that regulates the shape and position of the nucleus during cell migration. Mutations in this gene have been associated with infertility and also with an autosomal recessive form of intellectual disability (MRT47). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2017]","start":240014348,"end":240475189,"strand":1,"description":"formin 2 [Source:HGNC Symbol;Acc:HGNC:14074]"}, {"versioned_ensembl_gene_id":"ENSG00000171402.14","gene_symbol":"XAGE3","gene_name":"X antigen family member 3 [Source:HGNC Symbol;Acc:HGNC:14618]","synonyms":"XAGE-3,pp9012,PLAC6,GAGED4,CT12.3b,CT12.3a","biotype":"protein_coding","ncbi_id":"170626","summary":"This gene is a member of the XAGE subfamily, which belongs to the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. This gene is expressed in placenta and fetal liver/spleen, and may function in inhibiting cancer cell growth. The protein encoded by this gene shares a sequence similarity with other GAGE/PAGE proteins. Because of the expression pattern and the sequence similarity, this protein also belongs to a family of CT (cancer-testis) antigens. Alternative splicing of this gene generates 2 transcript variants differing in the 5' UTR. [provided by RefSeq, Jul 2008]","start":52862525,"end":52868068,"strand":-1,"description":"X antigen family member 3 [Source:HGNC Symbol;Acc:HGNC:14618]"}, {"versioned_ensembl_gene_id":"ENSG00000229015.2","gene_symbol":"AL450472.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135396429,"end":135397764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135341.17","gene_symbol":"MAP3K7","gene_name":"mitogen-activated protein kinase kinase kinase 7 [Source:HGNC Symbol;Acc:HGNC:6859]","synonyms":"TAK1,MEKK7","biotype":"protein_coding","ncbi_id":"6885","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase mediates the signaling transduction induced by TGF beta and morphogenetic protein (BMP), and controls a variety of cell functions including transcription regulation and apoptosis. In response to IL-1, this protein forms a kinase complex including TRAF6, MAP3K7P1/TAB1 and MAP3K7P2/TAB2; this complex is required for the activation of nuclear factor kappa B. This kinase can also activate MAPK8/JNK, MAP2K4/MKK4, and thus plays a role in the cell response to environmental stresses. Four alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":90513573,"end":90587045,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 7 [Source:HGNC Symbol;Acc:HGNC:6859]"}, {"versioned_ensembl_gene_id":"ENSG00000236492.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bQB10J12.1,bPG70P20.2,TIGD1L,bCX111D4.7","biotype":"processed_transcript","ncbi_id":"414771","summary":null,"start":30857662,"end":30866606,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000198003.11","gene_symbol":"CCDC151","gene_name":"coiled-coil domain containing 151 [Source:HGNC Symbol;Acc:HGNC:28303]","synonyms":"MGC20983","biotype":"protein_coding","ncbi_id":"115948","summary":"This gene encodes a protein containing coiled-coil domains. The encoded protein functions in outer dynein arm assembly and is required for motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":11420604,"end":11435782,"strand":-1,"description":"coiled-coil domain containing 151 [Source:HGNC Symbol;Acc:HGNC:28303]"}, {"versioned_ensembl_gene_id":"ENSG00000224017.1","gene_symbol":"LINC01449","gene_name":"long intergenic non-protein coding RNA 1449 [Source:HGNC Symbol;Acc:HGNC:50791]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928773","summary":null,"start":41101604,"end":41133507,"strand":1,"description":"long intergenic non-protein coding RNA 1449 [Source:HGNC Symbol;Acc:HGNC:50791]"}, {"versioned_ensembl_gene_id":"ENSG00000282809.1","gene_symbol":"MOXD2P","gene_name":"monooxygenase, DBH-like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33605]","synonyms":"MOXD2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100289017","summary":null,"start":142240759,"end":142247086,"strand":-1,"description":"monooxygenase, DBH-like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33605]"}, {"versioned_ensembl_gene_id":"ENSG00000224095.1","gene_symbol":"LINC01935","gene_name":"long intergenic non-protein coding RNA 1935 [Source:HGNC Symbol;Acc:HGNC:52758]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373519","summary":null,"start":102967408,"end":102984429,"strand":-1,"description":"long intergenic non-protein coding RNA 1935 [Source:HGNC Symbol;Acc:HGNC:52758]"}, {"versioned_ensembl_gene_id":"ENSG00000167604.14","gene_symbol":"NFKBID","gene_name":"NFKB inhibitor delta [Source:HGNC Symbol;Acc:HGNC:15671]","synonyms":"TA-NFKBH,IkappaBNS","biotype":"protein_coding","ncbi_id":"84807","summary":null,"start":35887653,"end":35902303,"strand":-1,"description":"NFKB inhibitor delta [Source:HGNC Symbol;Acc:HGNC:15671]"}, {"versioned_ensembl_gene_id":"ENSG00000181837.6","gene_symbol":"OR5D17P","gene_name":"olfactory receptor family 5 subfamily D member 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:15284]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81196","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55754976,"end":55755953,"strand":1,"description":"olfactory receptor family 5 subfamily D member 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:15284]"}, {"versioned_ensembl_gene_id":"ENSG00000186886.7","gene_symbol":"AP006437.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55723776,"end":55729621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279113.1","gene_symbol":"AC148477.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132332005,"end":132332432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231733.1","gene_symbol":"CR388215.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30830194,"end":30838828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159111.12","gene_symbol":"MRPL10","gene_name":"mitochondrial ribosomal protein L10 [Source:HGNC Symbol;Acc:HGNC:14055]","synonyms":"MRPL8,MRP-L8,MRP-L10,MGC17973,L10MT,RPML8","biotype":"protein_coding","ncbi_id":"124995","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Sequence analysis identified three transcript variants that encode two different isoforms. A pseudogene corresponding to this gene is found on chromosome 5q. [provided by RefSeq, Nov 2010]","start":47823272,"end":47831534,"strand":-1,"description":"mitochondrial ribosomal protein L10 [Source:HGNC Symbol;Acc:HGNC:14055]"}, {"versioned_ensembl_gene_id":"ENSG00000283644.1","gene_symbol":"ETDC","gene_name":"embryonic testis differentiation homolog C [Source:HGNC Symbol;Acc:HGNC:53450]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":135309480,"end":135309659,"strand":1,"description":"embryonic testis differentiation homolog C [Source:HGNC Symbol;Acc:HGNC:53450]"}, {"versioned_ensembl_gene_id":"ENSG00000233303.1","gene_symbol":"XXYLT1-AS1","gene_name":"XXYLT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41153]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874528","summary":null,"start":195094588,"end":195096057,"strand":1,"description":"XXYLT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41153]"}, {"versioned_ensembl_gene_id":"ENSG00000255633.5","gene_symbol":"MTRNR2L9","gene_name":"MT-RNR2-like 9 [Source:HGNC Symbol;Acc:HGNC:37166]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100463487","summary":null,"start":61574328,"end":61574402,"strand":1,"description":"MT-RNR2-like 9 [Source:HGNC Symbol;Acc:HGNC:37166]"}, {"versioned_ensembl_gene_id":"ENSG00000235010.1","gene_symbol":"AL512622.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132181225,"end":132185962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238210.3","gene_symbol":"ETDA","gene_name":"embryonic testis differentiation homolog A [Source:HGNC Symbol;Acc:HGNC:53449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928677","summary":null,"start":135252061,"end":135253583,"strand":1,"description":"embryonic testis differentiation homolog A [Source:HGNC Symbol;Acc:HGNC:53449]"}, {"versioned_ensembl_gene_id":"ENSG00000258421.2","gene_symbol":"FXNP1","gene_name":"frataxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20012]","synonyms":"FRDAP","biotype":"processed_pseudogene","ncbi_id":"122942","summary":null,"start":78059942,"end":78060278,"strand":-1,"description":"frataxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20012]"}, {"versioned_ensembl_gene_id":"ENSG00000236567.2","gene_symbol":"TCF3P1","gene_name":"transcription factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129107","summary":null,"start":5110913,"end":5112849,"strand":1,"description":"transcription factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49742]"}, {"versioned_ensembl_gene_id":"ENSG00000143486.15","gene_symbol":"EIF2D","gene_name":"eukaryotic translation initiation factor 2D [Source:HGNC Symbol;Acc:HGNC:6583]","synonyms":"LGTN","biotype":"protein_coding","ncbi_id":"1939","summary":"This gene encodes a translation initiation factor involved in the recruitment and delivery of aminoacyl-tRNAs to the P-site of the eukaryotic ribosome in a GTP-independent manner. This gene was previously referred to as ligatin, but is now known to localize to the cytoplasm and localize and function with translation factors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":206571292,"end":206612463,"strand":-1,"description":"eukaryotic translation initiation factor 2D [Source:HGNC Symbol;Acc:HGNC:6583]"}, {"versioned_ensembl_gene_id":"ENSG00000263618.5","gene_symbol":"AP005121.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14903580,"end":14915628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150281.6","gene_symbol":"CTF1","gene_name":"cardiotrophin 1 [Source:HGNC Symbol;Acc:HGNC:2499]","synonyms":"CT1,CT-1","biotype":"protein_coding","ncbi_id":"1489","summary":"The protein encoded by this gene is a secreted cytokine that induces cardiac myocyte hypertrophy in vitro. It has been shown to bind and activate the ILST/gp130 receoptor. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":30896607,"end":30903560,"strand":1,"description":"cardiotrophin 1 [Source:HGNC Symbol;Acc:HGNC:2499]"}, {"versioned_ensembl_gene_id":"ENSG00000248785.1","gene_symbol":"HIGD1AP14","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874455","summary":null,"start":109673843,"end":109674124,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:43009]"}, {"versioned_ensembl_gene_id":"ENSG00000152944.8","gene_symbol":"MED21","gene_name":"mediator complex subunit 21 [Source:HGNC Symbol;Acc:HGNC:11473]","synonyms":"SURB7,SRB7","biotype":"protein_coding","ncbi_id":"9412","summary":"This gene encodes a member of the mediator complex subunit 21 family. The encoded protein interacts with the human RNA polymerase II holoenzyme and is involved in transcriptional regulation of RNA polymerase II transcribed genes. A pseudogene of this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":27022546,"end":27066343,"strand":1,"description":"mediator complex subunit 21 [Source:HGNC Symbol;Acc:HGNC:11473]"}, {"versioned_ensembl_gene_id":"ENSG00000013275.7","gene_symbol":"PSMC4","gene_name":"proteasome 26S subunit, ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9551]","synonyms":"TBP7,TBP-7,S6,MIP224,MGC8570,MGC23214,MGC13687","biotype":"protein_coding","ncbi_id":"5704","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the triple-A family of ATPases that is a component of the 19S regulatory subunit and plays a role in 26S proteasome assembly. The encoded protein interacts with gankyrin, a liver oncoprotein, and may also play a role in Parkinson's disease through interactions with synphilin-1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":39971005,"end":39981441,"strand":1,"description":"proteasome 26S subunit, ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9551]"}, {"versioned_ensembl_gene_id":"ENSG00000179213.13","gene_symbol":"SIGLECL1","gene_name":"SIGLEC family like 1 [Source:HGNC Symbol;Acc:HGNC:26856]","synonyms":"SIGLECP7,SIGLEC23P,FLJ40235,C19orf75","biotype":"protein_coding","ncbi_id":"284369","summary":null,"start":51246348,"end":51269330,"strand":1,"description":"SIGLEC family like 1 [Source:HGNC Symbol;Acc:HGNC:26856]"}, {"versioned_ensembl_gene_id":"ENSG00000265971.1","gene_symbol":"AC005828.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63454993,"end":63455817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135362.13","gene_symbol":"PRR5L","gene_name":"proline rich 5 like [Source:HGNC Symbol;Acc:HGNC:25878]","synonyms":"PROTOR-2,FLJ14213","biotype":"protein_coding","ncbi_id":"79899","summary":null,"start":36296288,"end":36465204,"strand":1,"description":"proline rich 5 like [Source:HGNC Symbol;Acc:HGNC:25878]"}, {"versioned_ensembl_gene_id":"ENSG00000048405.9","gene_symbol":"ZNF800","gene_name":"zinc finger protein 800 [Source:HGNC Symbol;Acc:HGNC:27267]","synonyms":null,"biotype":"protein_coding","ncbi_id":"168850","summary":null,"start":127346790,"end":127431924,"strand":-1,"description":"zinc finger protein 800 [Source:HGNC Symbol;Acc:HGNC:27267]"}, {"versioned_ensembl_gene_id":"ENSG00000127838.13","gene_symbol":"PNKD","gene_name":"paroxysmal nonkinesigenic dyskinesia [Source:HGNC Symbol;Acc:HGNC:9153]","synonyms":"TAHCCP2,PKND1,PDC,MR-1,MGC31943,KIPP1184,KIAA1184,FPD1,FKSG19,DYT8,DKFZp564N1362,BRP17","biotype":"protein_coding","ncbi_id":"25953","summary":"This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":218270392,"end":218346793,"strand":1,"description":"paroxysmal nonkinesigenic dyskinesia [Source:HGNC Symbol;Acc:HGNC:9153]"}, {"versioned_ensembl_gene_id":"ENSG00000233232.6","gene_symbol":"NPIPB7","gene_name":"nuclear pore complex interacting protein family member B7 [Source:HGNC Symbol;Acc:HGNC:33832]","synonyms":"NPIPL1,LOC440350","biotype":"protein_coding","ncbi_id":"440350","summary":null,"start":28456372,"end":28471175,"strand":-1,"description":"nuclear pore complex interacting protein family member B7 [Source:HGNC Symbol;Acc:HGNC:33832]"}, {"versioned_ensembl_gene_id":"ENSG00000183671.12","gene_symbol":"GPR1","gene_name":"G protein-coupled receptor 1 [Source:HGNC Symbol;Acc:HGNC:4463]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2825","summary":null,"start":206175316,"end":206218047,"strand":-1,"description":"G protein-coupled receptor 1 [Source:HGNC Symbol;Acc:HGNC:4463]"}, {"versioned_ensembl_gene_id":"ENSG00000253557.5","gene_symbol":"AC100849.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19084992,"end":19259469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274954.1","gene_symbol":"AC090971.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51833134,"end":51833426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203446.2","gene_symbol":"AC004988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40538127,"end":40546928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275497.1","gene_symbol":"AC009237.17","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95633850,"end":95636106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256229.7","gene_symbol":"ZNF486","gene_name":"zinc finger protein 486 [Source:HGNC Symbol;Acc:HGNC:20807]","synonyms":"MGC2396,KRBO2","biotype":"protein_coding","ncbi_id":"90649","summary":null,"start":20167228,"end":20200490,"strand":1,"description":"zinc finger protein 486 [Source:HGNC Symbol;Acc:HGNC:20807]"}, {"versioned_ensembl_gene_id":"ENSG00000137561.4","gene_symbol":"TTPA","gene_name":"alpha tocopherol transfer protein [Source:HGNC Symbol;Acc:HGNC:12404]","synonyms":"AVED","biotype":"protein_coding","ncbi_id":"7274","summary":"This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa. [provided by RefSeq, Nov 2009]","start":63048553,"end":63086053,"strand":-1,"description":"alpha tocopherol transfer protein [Source:HGNC Symbol;Acc:HGNC:12404]"}, {"versioned_ensembl_gene_id":"ENSG00000116809.11","gene_symbol":"ZBTB17","gene_name":"zinc finger and BTB domain containing 17 [Source:HGNC Symbol;Acc:HGNC:12936]","synonyms":"ZNF60,ZNF151,pHZ-67,MIZ1","biotype":"protein_coding","ncbi_id":"7709","summary":"This gene encodes a zinc finger protein involved in the regulation of c-myc. The symbol MIZ1 has also been associated with PIAS2 which is a different gene located on chromosome 18. [provided by RefSeq, Jul 2008]","start":15941869,"end":15976132,"strand":-1,"description":"zinc finger and BTB domain containing 17 [Source:HGNC Symbol;Acc:HGNC:12936]"}, {"versioned_ensembl_gene_id":"ENSG00000273732.1","gene_symbol":"VN1R74P","gene_name":"vomeronasal 1 receptor 74 pseudogene [Source:HGNC Symbol;Acc:HGNC:37395]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312819","summary":null,"start":14680604,"end":14681106,"strand":-1,"description":"vomeronasal 1 receptor 74 pseudogene [Source:HGNC Symbol;Acc:HGNC:37395]"}, {"versioned_ensembl_gene_id":"ENSG00000241228.1","gene_symbol":"RPL12P31","gene_name":"ribosomal protein L12 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271406","summary":null,"start":35997226,"end":35997675,"strand":-1,"description":"ribosomal protein L12 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37025]"}, {"versioned_ensembl_gene_id":"ENSG00000236583.1","gene_symbol":"AP004290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99233048,"end":99234459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231979.1","gene_symbol":"AL356361.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239915439,"end":239916955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133019.11","gene_symbol":"CHRM3","gene_name":"cholinergic receptor muscarinic 3 [Source:HGNC Symbol;Acc:HGNC:1952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1131","summary":"The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The muscarinic cholinergic receptor 3 controls smooth muscle contraction and its stimulation causes secretion of glandular tissue. Alternative promoter use and alternative splicing results in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]","start":239386565,"end":239915452,"strand":1,"description":"cholinergic receptor muscarinic 3 [Source:HGNC Symbol;Acc:HGNC:1952]"}, {"versioned_ensembl_gene_id":"ENSG00000266605.1","gene_symbol":"AP006261.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14450216,"end":14450883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188816.3","gene_symbol":"HMX2","gene_name":"H6 family homeobox 2 [Source:HGNC Symbol;Acc:HGNC:5018]","synonyms":"NKX5-2","biotype":"protein_coding","ncbi_id":"3167","summary":"The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]","start":123148122,"end":123150672,"strand":1,"description":"H6 family homeobox 2 [Source:HGNC Symbol;Acc:HGNC:5018]"}, {"versioned_ensembl_gene_id":"ENSG00000238207.1","gene_symbol":"AC009312.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117757563,"end":117804174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169609.13","gene_symbol":"C15orf40","gene_name":"chromosome 15 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:28443]","synonyms":"MGC29937","biotype":"protein_coding","ncbi_id":"123207","summary":null,"start":82988441,"end":83011641,"strand":-1,"description":"chromosome 15 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:28443]"}, {"versioned_ensembl_gene_id":"ENSG00000119844.15","gene_symbol":"AFTPH","gene_name":"aftiphilin [Source:HGNC Symbol;Acc:HGNC:25951]","synonyms":"FLJ20080,Nbla10388,MGC33965,FLJ23793","biotype":"protein_coding","ncbi_id":"54812","summary":null,"start":64524305,"end":64593005,"strand":1,"description":"aftiphilin [Source:HGNC Symbol;Acc:HGNC:25951]"}, {"versioned_ensembl_gene_id":"ENSG00000271917.1","gene_symbol":"AL357568.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":164828436,"end":164829952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249321.1","gene_symbol":"OR5H5P","gene_name":"olfactory receptor family 5 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14765]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79297","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98197211,"end":98198138,"strand":1,"description":"olfactory receptor family 5 subfamily H member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14765]"}, {"versioned_ensembl_gene_id":"ENSG00000147481.14","gene_symbol":"SNTG1","gene_name":"syntrophin gamma 1 [Source:HGNC Symbol;Acc:HGNC:13740]","synonyms":"SYN4,G1SYN","biotype":"protein_coding","ncbi_id":"54212","summary":"The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]","start":49909789,"end":50794118,"strand":1,"description":"syntrophin gamma 1 [Source:HGNC Symbol;Acc:HGNC:13740]"}, {"versioned_ensembl_gene_id":"ENSG00000241472.6","gene_symbol":"PTPRG-AS1","gene_name":"PTPRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44638]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506994","summary":null,"start":62260865,"end":62369330,"strand":-1,"description":"PTPRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44638]"}, {"versioned_ensembl_gene_id":"ENSG00000185862.6","gene_symbol":"EVI2B","gene_name":"ecotropic viral integration site 2B [Source:HGNC Symbol;Acc:HGNC:3500]","synonyms":"CD361,EVDB,D17S376","biotype":"protein_coding","ncbi_id":"2124","summary":null,"start":31303766,"end":31314112,"strand":-1,"description":"ecotropic viral integration site 2B [Source:HGNC Symbol;Acc:HGNC:3500]"}, {"versioned_ensembl_gene_id":"ENSG00000114859.15","gene_symbol":"CLCN2","gene_name":"chloride voltage-gated channel 2 [Source:HGNC Symbol;Acc:HGNC:2020]","synonyms":"EJM6,CLC2,ClC-2","biotype":"protein_coding","ncbi_id":"1181","summary":"This gene encodes a voltage-gated chloride channel. The encoded protein is a transmembrane protein that maintains chloride ion homeostasis in various cells. Defects in this gene may be a cause of certain epilepsies. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":184346185,"end":184361651,"strand":-1,"description":"chloride voltage-gated channel 2 [Source:HGNC Symbol;Acc:HGNC:2020]"}, {"versioned_ensembl_gene_id":"ENSG00000256542.2","gene_symbol":"AC148477.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132277349,"end":132280900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163568.14","gene_symbol":"AIM2","gene_name":"absent in melanoma 2 [Source:HGNC Symbol;Acc:HGNC:357]","synonyms":"PYHIN4","biotype":"protein_coding","ncbi_id":"9447","summary":" AIM2 is a member of the IFI20X /IFI16 family. It plays a putative role in tumorigenic reversion and may control cell proliferation. Interferon-gamma induces expression of AIM2. [provided by RefSeq, Jul 2008]","start":159062484,"end":159147096,"strand":-1,"description":"absent in melanoma 2 [Source:HGNC Symbol;Acc:HGNC:357]"}, {"versioned_ensembl_gene_id":"ENSG00000230835.1","gene_symbol":"AP001187.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64881535,"end":64881945,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103942.12","gene_symbol":"HOMER2","gene_name":"homer scaffolding protein 2 [Source:HGNC Symbol;Acc:HGNC:17513]","synonyms":"Vesl-2,HOMER-2B,HOMER-2A,HOMER-2,CPD,Cupidin","biotype":"protein_coding","ncbi_id":"9455","summary":"This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. The encoded protein is a postsynaptic density scaffolding protein. Alternative splicing results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 14. [provided by RefSeq, Jun 2011]","start":82836946,"end":82986153,"strand":-1,"description":"homer scaffolding protein 2 [Source:HGNC Symbol;Acc:HGNC:17513]"}, {"versioned_ensembl_gene_id":"ENSG00000173890.16","gene_symbol":"GPR160","gene_name":"G protein-coupled receptor 160 [Source:HGNC Symbol;Acc:HGNC:23693]","synonyms":"GPCR150,GPCR1","biotype":"protein_coding","ncbi_id":"26996","summary":null,"start":170037929,"end":170085403,"strand":1,"description":"G protein-coupled receptor 160 [Source:HGNC Symbol;Acc:HGNC:23693]"}, {"versioned_ensembl_gene_id":"ENSG00000112877.7","gene_symbol":"CEP72","gene_name":"centrosomal protein 72 [Source:HGNC Symbol;Acc:HGNC:25547]","synonyms":"KIAA1519,FLJ10565","biotype":"protein_coding","ncbi_id":"55722","summary":"The product of this gene is a member of the leucine-rich-repeat (LRR) superfamily of proteins. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. [provided by RefSeq, Jul 2008]","start":612272,"end":667168,"strand":1,"description":"centrosomal protein 72 [Source:HGNC Symbol;Acc:HGNC:25547]"}, {"versioned_ensembl_gene_id":"ENSG00000154269.14","gene_symbol":"ENPP3","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 3 [Source:HGNC Symbol;Acc:HGNC:3358]","synonyms":"PDNP3,PD-IBETA,gp130RB13-6,CD203c,B10","biotype":"protein_coding","ncbi_id":"5169","summary":"The protein encoded by this gene belongs to a series of ectoenzymes that are involved in hydrolysis of extracellular nucleotides. These ectoenzymes possess ATPase and ATP pyrophosphatase activities and are type II transmembrane proteins. Expression of the related rat mRNA has been found in a subset of immature glial cells and in the alimentary tract. The corresponding rat protein has been detected in the pancreas, small intestine, colon, and liver. The human mRNA is expressed in glioma cells, prostate, and uterus. Expression of the human protein has been detected in uterus, basophils, and mast cells. Two transcript variants, one protein coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Oct 2015]","start":131628442,"end":131747418,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 3 [Source:HGNC Symbol;Acc:HGNC:3358]"}, {"versioned_ensembl_gene_id":"ENSG00000233412.5","gene_symbol":"OR5H15","gene_name":"olfactory receptor family 5 subfamily H member 15 [Source:HGNC Symbol;Acc:HGNC:31287]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403274","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98166696,"end":98169774,"strand":1,"description":"olfactory receptor family 5 subfamily H member 15 [Source:HGNC Symbol;Acc:HGNC:31287]"}, {"versioned_ensembl_gene_id":"ENSG00000218300.1","gene_symbol":"AL353692.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89876544,"end":89876878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116830.11","gene_symbol":"TTF2","gene_name":"transcription termination factor 2 [Source:HGNC Symbol;Acc:HGNC:12398]","synonyms":"ZGRF6,HuF2","biotype":"protein_coding","ncbi_id":"8458","summary":"This gene encodes a member of the SWI2/SNF2 family of proteins, which play a critical role in altering protein-DNA interactions. The encoded protein has been shown to have dsDNA-dependent ATPase activity and RNA polymerase II termination activity. This protein interacts with cell division cycle 5-like, associates with human splicing complexes, and plays a role in pre-mRNA splicing. [provided by RefSeq, Jul 2008]","start":117060303,"end":117107453,"strand":1,"description":"transcription termination factor 2 [Source:HGNC Symbol;Acc:HGNC:12398]"}, {"versioned_ensembl_gene_id":"ENSG00000255283.3","gene_symbol":"AP005597.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55279447,"end":55284749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244694.7","gene_symbol":"PTCHD4","gene_name":"patched domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21345]","synonyms":"dJ402H5.2,C6orf138,FLJ41841","biotype":"protein_coding","ncbi_id":"442213","summary":null,"start":47878028,"end":48068689,"strand":-1,"description":"patched domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21345]"}, {"versioned_ensembl_gene_id":"ENSG00000008838.19","gene_symbol":"MED24","gene_name":"mediator complex subunit 24 [Source:HGNC Symbol;Acc:HGNC:22963]","synonyms":"TRAP100,THRAP4,MED5,KIAA0130,DRIP100,CRSP4,CRSP100","biotype":"protein_coding","ncbi_id":"9862","summary":"This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, possibly by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":40019097,"end":40061215,"strand":-1,"description":"mediator complex subunit 24 [Source:HGNC Symbol;Acc:HGNC:22963]"}, {"versioned_ensembl_gene_id":"ENSG00000223377.1","gene_symbol":"AC244098.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149758021,"end":149758295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250127.1","gene_symbol":"LINC02108","gene_name":"long intergenic non-protein coding RNA 2108 [Source:HGNC Symbol;Acc:HGNC:52963]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928600","summary":null,"start":58541567,"end":58558243,"strand":-1,"description":"long intergenic non-protein coding RNA 2108 [Source:HGNC Symbol;Acc:HGNC:52963]"}, {"versioned_ensembl_gene_id":"ENSG00000157764.12","gene_symbol":"BRAF","gene_name":"B-Raf proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1097]","synonyms":"BRAF1","biotype":"protein_coding","ncbi_id":"673","summary":"This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]","start":140719327,"end":140924764,"strand":-1,"description":"B-Raf proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1097]"}, {"versioned_ensembl_gene_id":"ENSG00000283157.1","gene_symbol":"AC012564.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104699479,"end":104703555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215149.3","gene_symbol":"KRT18P32","gene_name":"keratin 18 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:33401]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391179","summary":null,"start":238491358,"end":238492644,"strand":1,"description":"keratin 18 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:33401]"}, {"versioned_ensembl_gene_id":"ENSG00000229322.1","gene_symbol":"AC244197.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149649174,"end":149650124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234464.1","gene_symbol":"AL356010.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":238276037,"end":238287016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257125.1","gene_symbol":"KRT127P","gene_name":"keratin 127 pseudogene [Source:HGNC Symbol;Acc:HGNC:40019]","synonyms":"KRT3P1","biotype":"unprocessed_pseudogene","ncbi_id":"100418779","summary":null,"start":52751978,"end":52753821,"strand":-1,"description":"keratin 127 pseudogene [Source:HGNC Symbol;Acc:HGNC:40019]"}, {"versioned_ensembl_gene_id":"ENSG00000232626.3","gene_symbol":"AC099336.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":202438396,"end":202439957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125492.9","gene_symbol":"BARHL1","gene_name":"BarH like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56751","summary":null,"start":132582185,"end":132590266,"strand":1,"description":"BarH like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:953]"}, {"versioned_ensembl_gene_id":"ENSG00000136738.14","gene_symbol":"STAM","gene_name":"signal transducing adaptor molecule [Source:HGNC Symbol;Acc:HGNC:11357]","synonyms":"STAM1","biotype":"protein_coding","ncbi_id":"8027","summary":"This gene encodes a member of the signal-transducing adaptor molecule family. These proteins mediate downstream signaling of cytokine receptors and also play a role in ER to Golgi trafficking by interacting with the coat protein II complex. The encoded protein also associates with hepatocyte growth factor-regulated substrate to form the endosomal sorting complex required for transport-0 (ESCRT-0), which sorts ubiquitinated membrane proteins to the ESCRT-1 complex for lysosomal degradation. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]","start":17644125,"end":17715914,"strand":1,"description":"signal transducing adaptor molecule [Source:HGNC Symbol;Acc:HGNC:11357]"}, {"versioned_ensembl_gene_id":"ENSG00000237224.4","gene_symbol":"AL157832.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129693722,"end":129702117,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274678.1","gene_symbol":"AC106886.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30821338,"end":30821884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268784.1","gene_symbol":"AC016629.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58582024,"end":58582609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255202.1","gene_symbol":"AL049629.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33665220,"end":33696701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258988.1","gene_symbol":"AL135978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67199062,"end":67200327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270025.2","gene_symbol":"BMS1P7","gene_name":"BMS1, ribosome biogenesis factor pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23655]","synonyms":"OTTHUMG00000018163,BMS1LP7,bA164N7.1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100133265","summary":null,"start":48050282,"end":48060016,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23655]"}, {"versioned_ensembl_gene_id":"ENSG00000255417.1","gene_symbol":"MTCO2P15","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52031]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075147","summary":null,"start":103403512,"end":103404167,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52031]"}, {"versioned_ensembl_gene_id":"ENSG00000156006.4","gene_symbol":"NAT2","gene_name":"N-acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:7646]","synonyms":"AAC2","biotype":"protein_coding","ncbi_id":"10","summary":"This gene encodes an enzyme that functions to both activate and deactivate arylamine and hydrazine drugs and carcinogens. Polymorphisms in this gene are responsible for the N-acetylation polymorphism in which human populations segregate into rapid, intermediate, and slow acetylator phenotypes. Polymorphisms in this gene are also associated with higher incidences of cancer and drug toxicity. A second polymorphic arylamine N-acetyltransferase gene (NAT1), is located near this gene (NAT2). [provided by RefSeq, Sep 2019]","start":18391245,"end":18401218,"strand":1,"description":"N-acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:7646]"}, {"versioned_ensembl_gene_id":"ENSG00000140521.12","gene_symbol":"POLG","gene_name":"DNA polymerase gamma, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9179]","synonyms":"POLGA,POLG1","biotype":"protein_coding","ncbi_id":"5428","summary":"Mitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N-terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO), Alpers-Huttenlocher syndrome (AHS), and mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":89305198,"end":89334861,"strand":-1,"description":"DNA polymerase gamma, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9179]"}, {"versioned_ensembl_gene_id":"ENSG00000237212.1","gene_symbol":"AL449403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96095211,"end":96101912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271654.1","gene_symbol":"AC025062.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18387108,"end":18387777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271983.1","gene_symbol":"AC023302.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80693216,"end":80693707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267150.1","gene_symbol":"AC006557.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14089935,"end":14091019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136379.11","gene_symbol":"ABHD17C","gene_name":"abhydrolase domain containing 17C [Source:HGNC Symbol;Acc:HGNC:26925]","synonyms":"FAM108C1","biotype":"protein_coding","ncbi_id":"58489","summary":null,"start":80679684,"end":80755621,"strand":1,"description":"abhydrolase domain containing 17C [Source:HGNC Symbol;Acc:HGNC:26925]"}, {"versioned_ensembl_gene_id":"ENSG00000267356.1","gene_symbol":"AC006557.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14104542,"end":14105226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275365.3","gene_symbol":"MMP11","gene_name":"matrix metallopeptidase 11 [Source:HGNC Symbol;Acc:HGNC:7157]","synonyms":"STMY3","biotype":"protein_coding","ncbi_id":"4320","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the enzyme encoded by this gene is activated intracellularly by furin within the constitutive secretory pathway. Also in contrast to other MMP's, this enzyme cleaves alpha 1-proteinase inhibitor but weakly degrades structural proteins of the extracellular matrix. [provided by RefSeq, Jul 2008]","start":23768226,"end":23784316,"strand":1,"description":"matrix metallopeptidase 11 [Source:HGNC Symbol;Acc:HGNC:7157]"}, {"versioned_ensembl_gene_id":"ENSG00000038295.7","gene_symbol":"TLL1","gene_name":"tolloid like 1 [Source:HGNC Symbol;Acc:HGNC:11843]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7092","summary":"This gene encodes an astacin-like, zinc-dependent, metalloprotease that belongs to the peptidase M12A family. This protease processes procollagen C-propeptides, such as chordin, pro-biglycan and pro-lysyl oxidase. Studies in mice suggest that this gene plays multiple roles in the development of mammalian heart, and is essential for the formation of the interventricular septum. Allelic variants of this gene are associated with atrial septal defect type 6. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":165873258,"end":166103895,"strand":1,"description":"tolloid like 1 [Source:HGNC Symbol;Acc:HGNC:11843]"}, {"versioned_ensembl_gene_id":"ENSG00000140386.12","gene_symbol":"SCAPER","gene_name":"S-phase cyclin A associated protein in the ER [Source:HGNC Symbol;Acc:HGNC:13081]","synonyms":"ZNF291,Zfp291","biotype":"protein_coding","ncbi_id":"49855","summary":null,"start":76347904,"end":76905444,"strand":-1,"description":"S-phase cyclin A associated protein in the ER [Source:HGNC Symbol;Acc:HGNC:13081]"}, {"versioned_ensembl_gene_id":"ENSG00000112706.11","gene_symbol":"IMPG1","gene_name":"interphotoreceptor matrix proteoglycan 1 [Source:HGNC Symbol;Acc:HGNC:6055]","synonyms":"SPACR,IPM150,GP147","biotype":"protein_coding","ncbi_id":"3617","summary":"This gene encodes a protein that is a major component of the retinal interphotoreceptor matrix. The encoded protein is a proteoglycan that is thought to play a role in maintaining viability of photoreceptor cells and in adhesion of the neural retina to the retinal pigment epithelium. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":75921115,"end":76072678,"strand":-1,"description":"interphotoreceptor matrix proteoglycan 1 [Source:HGNC Symbol;Acc:HGNC:6055]"}, {"versioned_ensembl_gene_id":"ENSG00000196517.11","gene_symbol":"SLC6A9","gene_name":"solute carrier family 6 member 9 [Source:HGNC Symbol;Acc:HGNC:11056]","synonyms":"GLYT1","biotype":"protein_coding","ncbi_id":"6536","summary":"The amino acid glycine acts as an inhibitory neurotransmitter in the central nervous system. The protein encoded by this gene is one of two transporters that stop glycine signaling by removing it from the synaptic cleft. [provided by RefSeq, Jun 2016]","start":43991500,"end":44031467,"strand":-1,"description":"solute carrier family 6 member 9 [Source:HGNC Symbol;Acc:HGNC:11056]"}, {"versioned_ensembl_gene_id":"ENSG00000233160.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32364622,"end":32365581,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000119421.6","gene_symbol":"NDUFA8","gene_name":"NADH:ubiquinone oxidoreductase subunit A8 [Source:HGNC Symbol;Acc:HGNC:7692]","synonyms":"PGIV,MGC793","biotype":"protein_coding","ncbi_id":"4702","summary":"The protein encoded by this gene belongs to the complex I 19 kDa subunit family. Mammalian complex I is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It plays an important role in transfering electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":122144058,"end":122159819,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A8 [Source:HGNC Symbol;Acc:HGNC:7692]"}, {"versioned_ensembl_gene_id":"ENSG00000255346.9","gene_symbol":"NOX5","gene_name":"NADPH oxidase 5 [Source:HGNC Symbol;Acc:HGNC:14874]","synonyms":"NOX5B,NOX5A","biotype":"protein_coding","ncbi_id":"79400","summary":"This gene is predominantly expressed in the testis and lymphocyte-rich areas of spleen and lymph nodes. It encodes a calcium-dependen NADPH oxidase that generates superoxide, and functions as a calcium-dependent proton channel that may regulate redox-dependent processes in lymphocytes and spermatozoa. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":68930525,"end":69062743,"strand":1,"description":"NADPH oxidase 5 [Source:HGNC Symbol;Acc:HGNC:14874]"}, {"versioned_ensembl_gene_id":"ENSG00000137808.12","gene_symbol":"AC027088.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":68930504,"end":69028889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185163.9","gene_symbol":"DDX51","gene_name":"DEAD-box helicase 51 [Source:HGNC Symbol;Acc:HGNC:20082]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317781","summary":null,"start":132136594,"end":132144335,"strand":-1,"description":"DEAD-box helicase 51 [Source:HGNC Symbol;Acc:HGNC:20082]"}, {"versioned_ensembl_gene_id":"ENSG00000231794.5","gene_symbol":"AC009542.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135198401,"end":135209837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235852.1","gene_symbol":"AC005540.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190880797,"end":190882059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157837.15","gene_symbol":"SPPL3","gene_name":"signal peptide peptidase like 3 [Source:HGNC Symbol;Acc:HGNC:30424]","synonyms":"MGC126674,IMP2,DKFZP586C1324,PSL4,MGC90402,MGC126676","biotype":"protein_coding","ncbi_id":"121665","summary":null,"start":120762510,"end":120904371,"strand":-1,"description":"signal peptide peptidase like 3 [Source:HGNC Symbol;Acc:HGNC:30424]"}, {"versioned_ensembl_gene_id":"ENSG00000149516.13","gene_symbol":"MS4A3","gene_name":"membrane spanning 4-domains A3 [Source:HGNC Symbol;Acc:HGNC:7317]","synonyms":"HTM4,CD20L","biotype":"protein_coding","ncbi_id":"932","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This family member likely plays a role in signal transduction and may function as a subunit associated with receptor complexes. The gene encoding this protein is localized to 11q12, among a cluster of related family members. Alternative splicing may result in multiple transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":60056587,"end":60071128,"strand":1,"description":"membrane spanning 4-domains A3 [Source:HGNC Symbol;Acc:HGNC:7317]"}, {"versioned_ensembl_gene_id":"ENSG00000119906.11","gene_symbol":"SLF2","gene_name":"SMC5-SMC6 complex localization factor 2 [Source:HGNC Symbol;Acc:HGNC:17814]","synonyms":"FLJ25012,FLJ10512,FAM178A,C10orf6","biotype":"protein_coding","ncbi_id":"55719","summary":null,"start":100912569,"end":100965136,"strand":1,"description":"SMC5-SMC6 complex localization factor 2 [Source:HGNC Symbol;Acc:HGNC:17814]"}, {"versioned_ensembl_gene_id":"ENSG00000244253.1","gene_symbol":"RPS29P24","gene_name":"ribosomal protein S29 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35794]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271589","summary":null,"start":39588955,"end":39589125,"strand":1,"description":"ribosomal protein S29 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35794]"}, {"versioned_ensembl_gene_id":"ENSG00000249816.6","gene_symbol":"LINC00964","gene_name":"long intergenic non-protein coding RNA 964 [Source:HGNC Symbol;Acc:HGNC:27226]","synonyms":null,"biotype":"lincRNA","ncbi_id":"157381","summary":null,"start":124848737,"end":124954328,"strand":1,"description":"long intergenic non-protein coding RNA 964 [Source:HGNC Symbol;Acc:HGNC:27226]"}, {"versioned_ensembl_gene_id":"ENSG00000176396.10","gene_symbol":"EID2","gene_name":"EP300 interacting inhibitor of differentiation 2 [Source:HGNC Symbol;Acc:HGNC:28292]","synonyms":"MGC20452,EID-2,CRI2","biotype":"protein_coding","ncbi_id":"163126","summary":null,"start":39538705,"end":39540333,"strand":-1,"description":"EP300 interacting inhibitor of differentiation 2 [Source:HGNC Symbol;Acc:HGNC:28292]"}, {"versioned_ensembl_gene_id":"ENSG00000072210.18","gene_symbol":"ALDH3A2","gene_name":"aldehyde dehydrogenase 3 family member A2 [Source:HGNC Symbol;Acc:HGNC:403]","synonyms":"SLS,FALDH,ALDH10","biotype":"protein_coding","ncbi_id":"224","summary":"Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":19648136,"end":19677598,"strand":1,"description":"aldehyde dehydrogenase 3 family member A2 [Source:HGNC Symbol;Acc:HGNC:403]"}, {"versioned_ensembl_gene_id":"ENSG00000269792.1","gene_symbol":"AC011500.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39532412,"end":39534422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176401.5","gene_symbol":"EID2B","gene_name":"EP300 interacting inhibitor of differentiation 2B [Source:HGNC Symbol;Acc:HGNC:26796]","synonyms":"FLJ38944,EID-3","biotype":"protein_coding","ncbi_id":"126272","summary":null,"start":39530990,"end":39532854,"strand":-1,"description":"EP300 interacting inhibitor of differentiation 2B [Source:HGNC Symbol;Acc:HGNC:26796]"}, {"versioned_ensembl_gene_id":"ENSG00000145241.10","gene_symbol":"CENPC","gene_name":"centromere protein C [Source:HGNC Symbol;Acc:HGNC:1854]","synonyms":"hcp-4,MIF2,CENPC1,CENP-C","biotype":"protein_coding","ncbi_id":"1060","summary":"Centromere protein C 1 is a centromere autoantigen and a component of the inner kinetochore plate. The protein is required for maintaining proper kinetochore size and a timely transition to anaphase. A putative pseudogene exists on chromosome 12. [provided by RefSeq, Jul 2008]","start":67468748,"end":67545606,"strand":-1,"description":"centromere protein C [Source:HGNC Symbol;Acc:HGNC:1854]"}, {"versioned_ensembl_gene_id":"ENSG00000259826.1","gene_symbol":"AC072061.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39947522,"end":39949755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278989.1","gene_symbol":"AP001148.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86434924,"end":86437282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240463.1","gene_symbol":"RPS19P3","gene_name":"ribosomal protein S19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728953","summary":null,"start":34568689,"end":34569129,"strand":-1,"description":"ribosomal protein S19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23560]"}, {"versioned_ensembl_gene_id":"ENSG00000072195.14","gene_symbol":"SPEG","gene_name":"SPEG complex locus [Source:HGNC Symbol;Acc:HGNC:16901]","synonyms":"SPEGbeta,SPEGalpha,MGC12676,KIAA1297,BPEG,APEG1","biotype":"protein_coding","ncbi_id":"10290","summary":"This gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Along with the desmin gene, expression of this gene may be controlled by the desmin locus control region. Mutations in this gene are associated with centronuclear myopathy 5. [provided by RefSeq, Jun 2016]","start":219434846,"end":219498287,"strand":1,"description":"SPEG complex locus [Source:HGNC Symbol;Acc:HGNC:16901]"}, {"versioned_ensembl_gene_id":"ENSG00000116260.16","gene_symbol":"QSOX1","gene_name":"quiescin sulfhydryl oxidase 1 [Source:HGNC Symbol;Acc:HGNC:9756]","synonyms":"QSCN6","biotype":"protein_coding","ncbi_id":"5768","summary":"This gene encodes a protein that contains domains of thioredoxin and ERV1, members of two long-standing gene families. The gene expression is induced as fibroblasts begin to exit the proliferative cycle and enter quiescence, suggesting that this gene plays an important role in growth regulation. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":180154834,"end":180204030,"strand":1,"description":"quiescin sulfhydryl oxidase 1 [Source:HGNC Symbol;Acc:HGNC:9756]"}, {"versioned_ensembl_gene_id":"ENSG00000262766.1","gene_symbol":"AC135050.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31118078,"end":31118747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103510.19","gene_symbol":"KAT8","gene_name":"lysine acetyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:17933]","synonyms":"ZC2HC8,MYST1,MOF,hMOF,FLJ14040","biotype":"protein_coding","ncbi_id":"84148","summary":"This gene encodes a member of the MYST histone acetylase protein family. The encoded protein has a characteristic MYST domain containing an acetyl-CoA-binding site, a chromodomain typical of proteins which bind histones, and a C2HC-type zinc finger. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":31115754,"end":31131393,"strand":1,"description":"lysine acetyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:17933]"}, {"versioned_ensembl_gene_id":"ENSG00000225138.7","gene_symbol":"SLC9A3-AS1","gene_name":"SLC9A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40550]","synonyms":"UC011CLY.2","biotype":"processed_transcript","ncbi_id":"100288152","summary":null,"start":473236,"end":480884,"strand":1,"description":"SLC9A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40550]"}, {"versioned_ensembl_gene_id":"ENSG00000248293.1","gene_symbol":"AC008413.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":174926541,"end":174926717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279660.1","gene_symbol":"AC005703.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15260513,"end":15261841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267085.1","gene_symbol":"AL512605.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65222522,"end":65222777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236252.2","gene_symbol":"AL512605.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":65219987,"end":65230861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197363.9","gene_symbol":"ZNF517","gene_name":"zinc finger protein 517 [Source:HGNC Symbol;Acc:HGNC:27984]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340385","summary":null,"start":144798876,"end":144811169,"strand":1,"description":"zinc finger protein 517 [Source:HGNC Symbol;Acc:HGNC:27984]"}, {"versioned_ensembl_gene_id":"ENSG00000273474.1","gene_symbol":"AL157392.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13675646,"end":13675990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102543.14","gene_symbol":"CDADC1","gene_name":"cytidine and dCMP deaminase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20299]","synonyms":"NYD-SP15","biotype":"protein_coding","ncbi_id":"81602","summary":null,"start":49247925,"end":49293485,"strand":1,"description":"cytidine and dCMP deaminase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20299]"}, {"versioned_ensembl_gene_id":"ENSG00000078808.16","gene_symbol":"SDF4","gene_name":"stromal cell derived factor 4 [Source:HGNC Symbol;Acc:HGNC:24188]","synonyms":"Cab45","biotype":"protein_coding","ncbi_id":"51150","summary":"This gene encodes a stromal cell derived factor that is a member of the CREC protein family. The encoded protein contains six EF-hand motifs and calcium-binding motifs. This protein localizes to the Golgi lumen and may be involved in regulating calcium dependent cellular activities. [provided by RefSeq, Sep 2011]","start":1216908,"end":1232031,"strand":-1,"description":"stromal cell derived factor 4 [Source:HGNC Symbol;Acc:HGNC:24188]"}, {"versioned_ensembl_gene_id":"ENSG00000253290.1","gene_symbol":"AC069113.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27903229,"end":27903495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226847.1","gene_symbol":"PRPS1P1","gene_name":"phosphoribosyl pyrophosphate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39427]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861436","summary":null,"start":164213539,"end":164214414,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39427]"}, {"versioned_ensembl_gene_id":"ENSG00000220161.4","gene_symbol":"LINC02076","gene_name":"long intergenic non-protein coding RNA 2076 [Source:HGNC Symbol;Acc:HGNC:52924]","synonyms":"FLJ35934","biotype":"lincRNA","ncbi_id":"400579","summary":null,"start":18411159,"end":18414380,"strand":1,"description":"long intergenic non-protein coding RNA 2076 [Source:HGNC Symbol;Acc:HGNC:52924]"}, {"versioned_ensembl_gene_id":"ENSG00000230282.1","gene_symbol":"RPL7P61","gene_name":"ribosomal protein L7 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:49217]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929589","summary":null,"start":163152251,"end":163153307,"strand":-1,"description":"ribosomal protein L7 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:49217]"}, {"versioned_ensembl_gene_id":"ENSG00000267980.1","gene_symbol":"AC007292.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4363789,"end":4364640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267545.1","gene_symbol":"AC005779.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":45179822,"end":45202444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179577.3","gene_symbol":"AP003471.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":104419512,"end":104421500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166902.4","gene_symbol":"MRPL16","gene_name":"mitochondrial ribosomal protein L16 [Source:HGNC Symbol;Acc:HGNC:14476]","synonyms":"PNAS-111,FLJ20484","biotype":"protein_coding","ncbi_id":"54948","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":59806135,"end":59810872,"strand":-1,"description":"mitochondrial ribosomal protein L16 [Source:HGNC Symbol;Acc:HGNC:14476]"}, {"versioned_ensembl_gene_id":"ENSG00000091140.13","gene_symbol":"DLD","gene_name":"dihydrolipoamide dehydrogenase [Source:HGNC Symbol;Acc:HGNC:2898]","synonyms":"LAD,GCSL,DLDH","biotype":"protein_coding","ncbi_id":"1738","summary":"This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":107890970,"end":107931730,"strand":1,"description":"dihydrolipoamide dehydrogenase [Source:HGNC Symbol;Acc:HGNC:2898]"}, {"versioned_ensembl_gene_id":"ENSG00000267441.1","gene_symbol":"AL353997.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18388871,"end":18389459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254944.1","gene_symbol":"ATP5F1P5","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39746]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128516","summary":null,"start":122960327,"end":122961086,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39746]"}, {"versioned_ensembl_gene_id":"ENSG00000214860.4","gene_symbol":"EVPLL","gene_name":"envoplakin like [Source:HGNC Symbol;Acc:HGNC:35236]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645027","summary":null,"start":18377662,"end":18389647,"strand":1,"description":"envoplakin like [Source:HGNC Symbol;Acc:HGNC:35236]"}, {"versioned_ensembl_gene_id":"ENSG00000121988.17","gene_symbol":"ZRANB3","gene_name":"zinc finger RANBP2-type containing 3 [Source:HGNC Symbol;Acc:HGNC:25249]","synonyms":"DKFZP434B1727","biotype":"protein_coding","ncbi_id":"84083","summary":null,"start":135136916,"end":135531236,"strand":-1,"description":"zinc finger RANBP2-type containing 3 [Source:HGNC Symbol;Acc:HGNC:25249]"}, {"versioned_ensembl_gene_id":"ENSG00000105520.10","gene_symbol":"PLPPR2","gene_name":"phospholipid phosphatase related 2 [Source:HGNC Symbol;Acc:HGNC:29566]","synonyms":"PRG-4,LPPR2","biotype":"protein_coding","ncbi_id":"64748","summary":null,"start":11355386,"end":11365698,"strand":1,"description":"phospholipid phosphatase related 2 [Source:HGNC Symbol;Acc:HGNC:29566]"}, {"versioned_ensembl_gene_id":"ENSG00000279093.1","gene_symbol":"AP001362.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":65561484,"end":65561607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259175.1","gene_symbol":"AC108451.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80554609,"end":80562944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189114.6","gene_symbol":"BLOC1S3","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 3 [Source:HGNC Symbol;Acc:HGNC:20914]","synonyms":"HPS8,BLOS3","biotype":"protein_coding","ncbi_id":"388552","summary":"This gene encodes a protein that is a component of the BLOC1 multi-subunit protein complex. This complex is necessary for the biogenesis of specialized organelles of the endosomal-lysosomal system, including platelet dense granules and melanosomes. Mutations in this gene cause Hermansky-Pudlak syndrome 8, a disease characterized by lysosomal storage defects, bleeding due to platelet storage pool deficiency, and oculocutaneous albinism. [provided by RefSeq, Jul 2008]","start":45178745,"end":45181801,"strand":1,"description":"biogenesis of lysosomal organelles complex 1 subunit 3 [Source:HGNC Symbol;Acc:HGNC:20914]"}, {"versioned_ensembl_gene_id":"ENSG00000115839.17","gene_symbol":"RAB3GAP1","gene_name":"RAB3 GTPase activating protein catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:17063]","synonyms":"WARBM1,RAB3GAP130,RAB3GAP,KIAA0066","biotype":"protein_coding","ncbi_id":"22930","summary":"This gene encodes the catalytic subunit of a Rab GTPase activating protein. The encoded protein forms a heterodimer with a non-catalytic subunit to specifically regulate the activity of members of the Rab3 subfamily of small G proteins. This protein mediates the hydrolysis of GTP bound Rab3 to the GDP bound form. Mutations in this gene are associated with Warburg micro syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]","start":135052265,"end":135176394,"strand":1,"description":"RAB3 GTPase activating protein catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:17063]"}, {"versioned_ensembl_gene_id":"ENSG00000258010.3","gene_symbol":"AC016705.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80433795,"end":80445152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260233.3","gene_symbol":"SSSCA1-AS1","gene_name":"SSSCA1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27384]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"254100","summary":null,"start":65568482,"end":65570423,"strand":-1,"description":"SSSCA1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27384]"}, {"versioned_ensembl_gene_id":"ENSG00000270919.1","gene_symbol":"AC108451.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80580029,"end":80580566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275206.1","gene_symbol":"AL353997.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18390153,"end":18390323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271918.1","gene_symbol":"AC034236.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116083807,"end":116085416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165794.9","gene_symbol":"SLC39A2","gene_name":"solute carrier family 39 member 2 [Source:HGNC Symbol;Acc:HGNC:17127]","synonyms":"ZIP2","biotype":"protein_coding","ncbi_id":"29986","summary":"This gene encodes a member of the ZIP family of metal ion transporters. The encoded protein functions as a zinc transporter. Mutations in this gene may be associated with susceptibility to carotid artery disease. Multiple transcript variants have been described. [provided by RefSeq, Mar 2010]","start":20999255,"end":21001871,"strand":1,"description":"solute carrier family 39 member 2 [Source:HGNC Symbol;Acc:HGNC:17127]"}, {"versioned_ensembl_gene_id":"ENSG00000029639.10","gene_symbol":"TFB1M","gene_name":"transcription factor B1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17037]","synonyms":"mtTFB,CGI-75","biotype":"protein_coding","ncbi_id":"51106","summary":"The protein encoded by this gene is a dimethyltransferase that methylates the conserved stem loop of mitochondrial 12S rRNA. The encoded protein also is part of the basal mitochondrial transcription complex and is necessary for mitochondrial gene expression. The methylation and transcriptional activities of this protein are independent of one another. Variations in this gene may influence the severity of aminoglycoside-induced deafness (AID).[provided by RefSeq, Aug 2010]","start":155257509,"end":155314493,"strand":-1,"description":"transcription factor B1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17037]"}, {"versioned_ensembl_gene_id":"ENSG00000145781.8","gene_symbol":"COMMD10","gene_name":"COMM domain containing 10 [Source:HGNC Symbol;Acc:HGNC:30201]","synonyms":"PTD002","biotype":"protein_coding","ncbi_id":"51397","summary":null,"start":116084991,"end":116412762,"strand":1,"description":"COMM domain containing 10 [Source:HGNC Symbol;Acc:HGNC:30201]"}, {"versioned_ensembl_gene_id":"ENSG00000272277.1","gene_symbol":"AL031963.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3068045,"end":3068894,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283632.2","gene_symbol":"EXOC3L2","gene_name":"exocyst complex component 3 like 2 [Source:HGNC Symbol;Acc:HGNC:30162]","synonyms":"XTP7,FLJ36147","biotype":"protein_coding","ncbi_id":"90332","summary":"The protein encoded by this gene is upregulated by vascular endothelial growth factor A and interacts with exocyst complex component 4. The encoded protein may be part of an exocyst complex that plays a role in cell membrane dynamics. Mutations in this gene may be associated with Alzheimer's disease. [provided by RefSeq, May 2017]","start":45212621,"end":45245431,"strand":-1,"description":"exocyst complex component 3 like 2 [Source:HGNC Symbol;Acc:HGNC:30162]"}, {"versioned_ensembl_gene_id":"ENSG00000137275.13","gene_symbol":"RIPK1","gene_name":"receptor interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:10019]","synonyms":"RIP","biotype":"protein_coding","ncbi_id":"8737","summary":"This gene encodes a member of the receptor-interacting protein (RIP) family of serine/threonine protein kinases. The encoded protein plays a role in inflammation and cell death in response to tissue damage, pathogen recognition, and as part of developmental regulation. RIPK1/RIPK3 kinase-mediated necrosis is referred to as necroptosis. Genetic disruption of this gene in mice results in death shortly after birth. [provided by RefSeq, Aug 2017]","start":3063991,"end":3115187,"strand":1,"description":"receptor interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:10019]"}, {"versioned_ensembl_gene_id":"ENSG00000112379.8","gene_symbol":"ARFGEF3","gene_name":"ARFGEF family member 3 [Source:HGNC Symbol;Acc:HGNC:21213]","synonyms":"C6orf92,BIG3,PPP1R33,KIAA1244,dJ171N11.1","biotype":"protein_coding","ncbi_id":"57221","summary":null,"start":138161921,"end":138344663,"strand":1,"description":"ARFGEF family member 3 [Source:HGNC Symbol;Acc:HGNC:21213]"}, {"versioned_ensembl_gene_id":"ENSG00000229681.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30693326,"end":30703442,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000227060.6","gene_symbol":"LINC00629","gene_name":"long intergenic non-protein coding RNA 629 [Source:HGNC Symbol;Acc:HGNC:44262]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506757","summary":null,"start":134549973,"end":134559923,"strand":1,"description":"long intergenic non-protein coding RNA 629 [Source:HGNC Symbol;Acc:HGNC:44262]"}, {"versioned_ensembl_gene_id":"ENSG00000118193.11","gene_symbol":"KIF14","gene_name":"kinesin family member 14 [Source:HGNC Symbol;Acc:HGNC:19181]","synonyms":"KIAA0042","biotype":"protein_coding","ncbi_id":"9928","summary":"This gene encodes a member of the kinesin-3 superfamily of microtubule motor proteins. These proteins are involved in numerous processes including vesicle transport, chromosome segregation, mitotic spindle formation, and cytokinesis. In human HeLa-S3 and 293T cells, this protein is localized to the cytoplasm during interphase, to the spindle poles and spindle microtubules during mitosis, and to the midbody during cytokinesis. An internal motor domain displays microtubule-dependent ATPase activity, consistent with its function as a microtubule motor protein. Knockdown of this gene results in failed cytokinesis with endoreplication, which results in multinucleated cells. This gene has been identified as a likely oncogene in breast, lung and ovarian cancers, as well as retinoblastomas and gliomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":200551497,"end":200620734,"strand":-1,"description":"kinesin family member 14 [Source:HGNC Symbol;Acc:HGNC:19181]"}, {"versioned_ensembl_gene_id":"ENSG00000230240.1","gene_symbol":"RPL34P19","gene_name":"ribosomal protein L34 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271494","summary":null,"start":31983885,"end":31984554,"strand":1,"description":"ribosomal protein L34 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36925]"}, {"versioned_ensembl_gene_id":"ENSG00000007255.10","gene_symbol":"TRAPPC6A","gene_name":"trafficking protein particle complex 6A [Source:HGNC Symbol;Acc:HGNC:23069]","synonyms":"HSPC289,TRS33,MGC2650","biotype":"protein_coding","ncbi_id":"79090","summary":"This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. Loss of expression of the related gene in mouse affects coat and eye pigmentation, suggesting that the encoded protein may be involved in melanosome biogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":45162928,"end":45178237,"strand":-1,"description":"trafficking protein particle complex 6A [Source:HGNC Symbol;Acc:HGNC:23069]"}, {"versioned_ensembl_gene_id":"ENSG00000232873.1","gene_symbol":"RPL23AP93","gene_name":"ribosomal protein L23a pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:51628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288802","summary":null,"start":194562978,"end":194564001,"strand":-1,"description":"ribosomal protein L23a pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:51628]"}, {"versioned_ensembl_gene_id":"ENSG00000104972.15","gene_symbol":"LILRB1","gene_name":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]","synonyms":"CD85j,LIR1,PIRB,CD85,LIR-1,PIR-B,ILT2,MIR-7","biotype":"protein_coding","ncbi_id":"10859","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54617158,"end":54637528,"strand":1,"description":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]"}, {"versioned_ensembl_gene_id":"ENSG00000235813.1","gene_symbol":"AL672032.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134599457,"end":134606254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260262.1","gene_symbol":"AC139887.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":836512,"end":837224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237432.2","gene_symbol":"RPS7P12","gene_name":"ribosomal protein S7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36147]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270914","summary":null,"start":134650830,"end":134651411,"strand":1,"description":"ribosomal protein S7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36147]"}, {"versioned_ensembl_gene_id":"ENSG00000255190.2","gene_symbol":"TRIM51DP","gene_name":"tripartite motif-containing 51D, pseudogene [Source:HGNC Symbol;Acc:HGNC:43969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419945","summary":null,"start":49874945,"end":49876638,"strand":1,"description":"tripartite motif-containing 51D, pseudogene [Source:HGNC Symbol;Acc:HGNC:43969]"}, {"versioned_ensembl_gene_id":"ENSG00000237682.2","gene_symbol":"AC234775.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101537485,"end":101539276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170965.9","gene_symbol":"PLAC1","gene_name":"placenta specific 1 [Source:HGNC Symbol;Acc:HGNC:9044]","synonyms":"OOSP2L,CT92","biotype":"protein_coding","ncbi_id":"10761","summary":null,"start":134565838,"end":134764322,"strand":-1,"description":"placenta specific 1 [Source:HGNC Symbol;Acc:HGNC:9044]"}, {"versioned_ensembl_gene_id":"ENSG00000254800.2","gene_symbol":"AP006587.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49882999,"end":49884093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197702.11","gene_symbol":"PARVA","gene_name":"parvin alpha [Source:HGNC Symbol;Acc:HGNC:14652]","synonyms":"MXRA2,FLJ12254,FLJ10793","biotype":"protein_coding","ncbi_id":"55742","summary":"This gene encodes a member of the parvin family of actin-binding proteins. Parvins are associated with focal contacts and contain calponin homology domains that bind to actin filaments. The encoded protein is part of the integrin-linked kinase signaling complex and plays a role in cell adhesion, motility and survival. [provided by RefSeq, Dec 2010]","start":12377185,"end":12530801,"strand":1,"description":"parvin alpha [Source:HGNC Symbol;Acc:HGNC:14652]"}, {"versioned_ensembl_gene_id":"ENSG00000229216.4","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31558969,"end":31559780,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000226419.7","gene_symbol":"SLC16A1-AS1","gene_name":"SLC16A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49445]","synonyms":"ENST00000421157.1","biotype":"antisense_RNA","ncbi_id":"100506392","summary":null,"start":112956415,"end":113047055,"strand":1,"description":"SLC16A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49445]"}, {"versioned_ensembl_gene_id":"ENSG00000223001.1","gene_symbol":"RNU2-61P","gene_name":"RNA, U2 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:48554]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480673","summary":null,"start":89063500,"end":89063690,"strand":-1,"description":"RNA, U2 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:48554]"}, {"versioned_ensembl_gene_id":"ENSG00000212395.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"U67,RNU67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":131782860,"end":131782958,"strand":-1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000136807.13","gene_symbol":"CDK9","gene_name":"cyclin dependent kinase 9 [Source:HGNC Symbol;Acc:HGNC:1780]","synonyms":"CDC2L4,C-2k,TAK,PITALRE","biotype":"protein_coding","ncbi_id":"1025","summary":"The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, and known as important cell cycle regulators. This kinase was found to be a component of the multiprotein complex TAK/P-TEFb, which is an elongation factor for RNA polymerase II-directed transcription and functions by phosphorylating the C-terminal domain of the largest subunit of RNA polymerase II. This protein forms a complex with and is regulated by its regulatory subunit cyclin T or cyclin K. HIV-1 Tat protein was found to interact with this protein and cyclin T, which suggested a possible involvement of this protein in AIDS. [provided by RefSeq, Jul 2008]","start":127785679,"end":127790787,"strand":1,"description":"cyclin dependent kinase 9 [Source:HGNC Symbol;Acc:HGNC:1780]"}, {"versioned_ensembl_gene_id":"ENSG00000130584.10","gene_symbol":"ZBTB46","gene_name":"zinc finger and BTB domain containing 46 [Source:HGNC Symbol;Acc:HGNC:16094]","synonyms":"ZNF340,RINZF,FLJ13502,BZEL,BTBD4","biotype":"protein_coding","ncbi_id":"140685","summary":null,"start":63743666,"end":63831244,"strand":-1,"description":"zinc finger and BTB domain containing 46 [Source:HGNC Symbol;Acc:HGNC:16094]"}, {"versioned_ensembl_gene_id":"ENSG00000236509.2","gene_symbol":"RPL21P133","gene_name":"ribosomal protein L21 pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:36003]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271391","summary":null,"start":134607157,"end":134607632,"strand":1,"description":"ribosomal protein L21 pseudogene 133 [Source:HGNC Symbol;Acc:HGNC:36003]"}, {"versioned_ensembl_gene_id":"ENSG00000267667.1","gene_symbol":"AC005856.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61130704,"end":61135964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254114.1","gene_symbol":"HMGN1P28","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39372]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874464","summary":null,"start":60851382,"end":60851745,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39372]"}, {"versioned_ensembl_gene_id":"ENSG00000166263.13","gene_symbol":"STXBP4","gene_name":"syntaxin binding protein 4 [Source:HGNC Symbol;Acc:HGNC:19694]","synonyms":"Synip,MGC50337","biotype":"protein_coding","ncbi_id":"252983","summary":null,"start":54968727,"end":55173632,"strand":1,"description":"syntaxin binding protein 4 [Source:HGNC Symbol;Acc:HGNC:19694]"}, {"versioned_ensembl_gene_id":"ENSG00000231665.1","gene_symbol":"OGFOD1P1","gene_name":"2-oxoglutarate and iron dependent oxygenase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39202]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387924","summary":null,"start":49210422,"end":49212294,"strand":-1,"description":"2-oxoglutarate and iron dependent oxygenase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39202]"}, {"versioned_ensembl_gene_id":"ENSG00000232916.1","gene_symbol":"HMGN2P27","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39394]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874471","summary":null,"start":116218026,"end":116218295,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39394]"}, {"versioned_ensembl_gene_id":"ENSG00000224011.1","gene_symbol":"AC110602.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60727165,"end":60727482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250015.1","gene_symbol":"AC018752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116302354,"end":116304134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277191.1","gene_symbol":"AC138904.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28341437,"end":28341543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267131.1","gene_symbol":"AC005746.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61361668,"end":61400243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235381.1","gene_symbol":"AL596202.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155253139,"end":155256724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271177.1","gene_symbol":"AC010200.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100525186,"end":100525420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198156.10","gene_symbol":"NPIPB6","gene_name":"nuclear pore complex interacting protein family member B6 [Source:HGNC Symbol;Acc:HGNC:37454]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728741","summary":null,"start":28342555,"end":28363508,"strand":-1,"description":"nuclear pore complex interacting protein family member B6 [Source:HGNC Symbol;Acc:HGNC:37454]"}, {"versioned_ensembl_gene_id":"ENSG00000121068.13","gene_symbol":"TBX2","gene_name":"T-box 2 [Source:HGNC Symbol;Acc:HGNC:11597]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6909","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product is the human homolog of mouse Tbx2, and shares strong sequence similarity with Drosophila omb protein. Expression studies indicate that this gene may have a potential role in tumorigenesis as an immortalizing agent. Transcript heterogeneity due to alternative polyadenylation has been noted for this gene. [provided by RefSeq, Jul 2008]","start":61399896,"end":61409466,"strand":1,"description":"T-box 2 [Source:HGNC Symbol;Acc:HGNC:11597]"}, {"versioned_ensembl_gene_id":"ENSG00000218757.1","gene_symbol":"AL121952.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154845074,"end":154845620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171217.5","gene_symbol":"CLDN20","gene_name":"claudin 20 [Source:HGNC Symbol;Acc:HGNC:2042]","synonyms":null,"biotype":"protein_coding","ncbi_id":"49861","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. [provided by RefSeq, Jun 2010]","start":155264013,"end":155276548,"strand":1,"description":"claudin 20 [Source:HGNC Symbol;Acc:HGNC:2042]"}, {"versioned_ensembl_gene_id":"ENSG00000139132.14","gene_symbol":"FGD4","gene_name":"FYVE, RhoGEF and PH domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19125]","synonyms":"ZFYVE6,FRABP,frabin,CMT4H","biotype":"protein_coding","ncbi_id":"121512","summary":"This gene encodes a protein that is involved in the regulation of the actin cytoskeleton and cell shape. This protein contains an actin filament-binding domain, which together with its Dbl homology domain and one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-binding domain, and it is also involved in the activation of CDC42 via the exchange of bound GDP for free GTP. The activation of CDC42 also enables this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":32399529,"end":32646050,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19125]"}, {"versioned_ensembl_gene_id":"ENSG00000274451.1","gene_symbol":"AL136228.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155004835,"end":155005318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241255.1","gene_symbol":"AL136126.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33237008,"end":33237409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271623.1","gene_symbol":"AC138894.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28364700,"end":28365333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226781.1","gene_symbol":"TBCAP1","gene_name":"tubulin folding cofactor A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"494540","summary":null,"start":33041395,"end":33041721,"strand":1,"description":"tubulin folding cofactor A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42630]"}, {"versioned_ensembl_gene_id":"ENSG00000146426.17","gene_symbol":"TIAM2","gene_name":"T-cell lymphoma invasion and metastasis 2 [Source:HGNC Symbol;Acc:HGNC:11806]","synonyms":"STEF","biotype":"protein_coding","ncbi_id":"26230","summary":"This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras-related C3 botulinum substrate 1, converting this Rho-like guanosine triphosphatase (GTPase) from a guanosine diphosphate-bound inactive state to a guanosine triphosphate-bound active state. The encoded protein may play a role in neural cell development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":154832697,"end":155257723,"strand":1,"description":"T-cell lymphoma invasion and metastasis 2 [Source:HGNC Symbol;Acc:HGNC:11806]"}, {"versioned_ensembl_gene_id":"ENSG00000267348.2","gene_symbol":"AC011489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45076510,"end":45090391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223315.1","gene_symbol":"RN7SKP279","gene_name":"RNA, 7SK small nuclear pseudogene 279 [Source:HGNC Symbol;Acc:HGNC:46003]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480479","summary":null,"start":127407851,"end":127408148,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 279 [Source:HGNC Symbol;Acc:HGNC:46003]"}, {"versioned_ensembl_gene_id":"ENSG00000173465.7","gene_symbol":"SSSCA1","gene_name":"Sjogren syndrome/scleroderma autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11328]","synonyms":"p27","biotype":"protein_coding","ncbi_id":"10534","summary":"This antigen is recognized by a subset of anti-centromere antibodies from patients with scleroderma and/or Sjogren's syndrome. Subcellular localization has not yet been established. [provided by RefSeq, Jul 2008]","start":65570430,"end":65573942,"strand":1,"description":"Sjogren syndrome/scleroderma autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:11328]"}, {"versioned_ensembl_gene_id":"ENSG00000235026.5","gene_symbol":"DPP10-AS1","gene_name":"DPP10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40941]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"389023","summary":null,"start":115130935,"end":115161343,"strand":-1,"description":"DPP10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40941]"}, {"versioned_ensembl_gene_id":"ENSG00000223651.1","gene_symbol":"AL049812.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41997131,"end":41999397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137809.16","gene_symbol":"ITGA11","gene_name":"integrin subunit alpha 11 [Source:HGNC Symbol;Acc:HGNC:6136]","synonyms":"HsT18964","biotype":"protein_coding","ncbi_id":"22801","summary":"This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein contains an I domain, is expressed in muscle tissue, dimerizes with beta 1 integrin in vitro, and appears to bind collagen in this form. Therefore, the protein may be involved in attaching muscle tissue to the extracellular matrix. Alternative transcriptional splice variants have been found for this gene, but their biological validity is not determined. [provided by RefSeq, Jul 2008]","start":68296533,"end":68432162,"strand":-1,"description":"integrin subunit alpha 11 [Source:HGNC Symbol;Acc:HGNC:6136]"}, {"versioned_ensembl_gene_id":"ENSG00000279317.2","gene_symbol":"AC006994.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":210171518,"end":210233976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256364.1","gene_symbol":"AC069234.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120697124,"end":120699541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176136.6","gene_symbol":"MC5R","gene_name":"melanocortin 5 receptor [Source:HGNC Symbol;Acc:HGNC:6933]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4161","summary":"This gene encodes a member of the seven-pass transmembrane G protein-coupled melanocortin receptor protein family that stimulate cAMP signal transduction. The encoded protein is a receptor for melanocyte-stimulating hormone and adrenocorticotropic hormone and is suggested to play a role in sebum generation. [provided by RefSeq, Jun 2010]","start":13824149,"end":13827323,"strand":1,"description":"melanocortin 5 receptor [Source:HGNC Symbol;Acc:HGNC:6933]"}, {"versioned_ensembl_gene_id":"ENSG00000170684.8","gene_symbol":"ZNF296","gene_name":"zinc finger protein 296 [Source:HGNC Symbol;Acc:HGNC:15981]","synonyms":"ZNF342","biotype":"protein_coding","ncbi_id":"162979","summary":null,"start":45071500,"end":45076588,"strand":-1,"description":"zinc finger protein 296 [Source:HGNC Symbol;Acc:HGNC:15981]"}, {"versioned_ensembl_gene_id":"ENSG00000110917.7","gene_symbol":"MLEC","gene_name":"malectin [Source:HGNC Symbol;Acc:HGNC:28973]","synonyms":"KIAA0152","biotype":"protein_coding","ncbi_id":"9761","summary":"This gene encodes the carbohydrate-binding protein malectin which is a Type I membrane-anchored endoplasmic reticulum protein. This protein has an affinity for Glc2Man9GlcNAc2 (G2M9) N-glycans and is involved in regulating glycosylation in the endoplasmic reticulum. This protein has also been shown to interact with ribophorin I and may be involved in the directing the degradation of misfolded proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":120686869,"end":120701864,"strand":1,"description":"malectin [Source:HGNC Symbol;Acc:HGNC:28973]"}, {"versioned_ensembl_gene_id":"ENSG00000267280.5","gene_symbol":"TBX2-AS1","gene_name":"TBX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50355]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103689912","summary":null,"start":61393456,"end":61411555,"strand":-1,"description":"TBX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50355]"}, {"versioned_ensembl_gene_id":"ENSG00000115361.7","gene_symbol":"ACADL","gene_name":"acyl-CoA dehydrogenase, long chain [Source:HGNC Symbol;Acc:HGNC:88]","synonyms":"LCAD,ACAD4","biotype":"protein_coding","ncbi_id":"33","summary":"The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008]","start":210187939,"end":210225491,"strand":-1,"description":"acyl-CoA dehydrogenase, long chain [Source:HGNC Symbol;Acc:HGNC:88]"}, {"versioned_ensembl_gene_id":"ENSG00000231538.1","gene_symbol":"DPP10-AS3","gene_name":"DPP10 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40939]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927591","summary":null,"start":114828432,"end":114833548,"strand":-1,"description":"DPP10 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40939]"}, {"versioned_ensembl_gene_id":"ENSG00000225458.1","gene_symbol":"AL049812.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41991140,"end":42063969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198947.15","gene_symbol":"DMD","gene_name":"dystrophin [Source:HGNC Symbol;Acc:HGNC:2928]","synonyms":"BMD,DXS270,DXS269,DXS268,DXS239,DXS230,DXS206,DXS164,MRX85,DXS142,DXS272","biotype":"protein_coding","ncbi_id":"1756","summary":"This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [provided by RefSeq, Dec 2016]","start":31097677,"end":33339441,"strand":-1,"description":"dystrophin [Source:HGNC Symbol;Acc:HGNC:2928]"}, {"versioned_ensembl_gene_id":"ENSG00000225113.1","gene_symbol":"AL355310.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":109596225,"end":109597781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214510.9","gene_symbol":"SPINK13","gene_name":"serine peptidase inhibitor, Kazal type 13 (putative) [Source:HGNC Symbol;Acc:HGNC:27200]","synonyms":"SPINK5L3,MGC149260,LiESP6,HESPINTOR","biotype":"protein_coding","ncbi_id":"153218","summary":null,"start":148268180,"end":148286254,"strand":1,"description":"serine peptidase inhibitor, Kazal type 13 (putative) [Source:HGNC Symbol;Acc:HGNC:27200]"}, {"versioned_ensembl_gene_id":"ENSG00000175497.16","gene_symbol":"DPP10","gene_name":"dipeptidyl peptidase like 10 [Source:HGNC Symbol;Acc:HGNC:20823]","synonyms":"DPRP3,DPPY,DPL2","biotype":"protein_coding","ncbi_id":"57628","summary":"This gene encodes a single-pass type II membrane protein that is a member of the S9B family in clan SC of the serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Mutations in this gene have been associated with asthma. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":114442299,"end":115845752,"strand":1,"description":"dipeptidyl peptidase like 10 [Source:HGNC Symbol;Acc:HGNC:20823]"}, {"versioned_ensembl_gene_id":"ENSG00000229595.1","gene_symbol":"AL109810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231117831,"end":231118325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281374.1","gene_symbol":"AP000344.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":23446598,"end":23460833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185231.4","gene_symbol":"MC2R","gene_name":"melanocortin 2 receptor [Source:HGNC Symbol;Acc:HGNC:6930]","synonyms":"ACTHR","biotype":"protein_coding","ncbi_id":"4158","summary":"MC2R encodes one member of the five-member G-protein associated melanocortin receptor family. Melanocortins (melanocyte-stimulating hormones and adrenocorticotropic hormone) are peptides derived from pro-opiomelanocortin (POMC). MC2R is selectively activated by adrenocorticotropic hormone, whereas the other four melanocortin receptors recognize a variety of melanocortin ligands. Mutations in MC2R can result in familial glucocorticoid deficiency. Alternate transcript variants have been found for this gene. [provided by RefSeq, May 2014]","start":13882044,"end":13915707,"strand":-1,"description":"melanocortin 2 receptor [Source:HGNC Symbol;Acc:HGNC:6930]"}, {"versioned_ensembl_gene_id":"ENSG00000145014.17","gene_symbol":"TMEM44","gene_name":"transmembrane protein 44 [Source:HGNC Symbol;Acc:HGNC:25120]","synonyms":"DKFZp686O18124","biotype":"protein_coding","ncbi_id":"93109","summary":null,"start":194587673,"end":194633689,"strand":-1,"description":"transmembrane protein 44 [Source:HGNC Symbol;Acc:HGNC:25120]"}, {"versioned_ensembl_gene_id":"ENSG00000200502.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37160137,"end":37160237,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000138755.5","gene_symbol":"CXCL9","gene_name":"C-X-C motif chemokine ligand 9 [Source:HGNC Symbol;Acc:HGNC:7098]","synonyms":"SCYB9,MIG,Humig,crg-10,CMK","biotype":"protein_coding","ncbi_id":"4283","summary":"This antimicrobial gene is part of a chemokine superfamily that encodes secreted proteins involved in immunoregulatory and inflammatory processes. The protein encoded is thought to be involved in T cell trafficking. The encoded protein binds to C-X-C motif chemokine 3 and is a chemoattractant for lymphocytes but not for neutrophils. [provided by RefSeq, Aug 2020]","start":76001275,"end":76007488,"strand":-1,"description":"C-X-C motif chemokine ligand 9 [Source:HGNC Symbol;Acc:HGNC:7098]"}, {"versioned_ensembl_gene_id":"ENSG00000142252.10","gene_symbol":"GEMIN7","gene_name":"gem nuclear organelle associated protein 7 [Source:HGNC Symbol;Acc:HGNC:20045]","synonyms":"FLJ13956","biotype":"protein_coding","ncbi_id":"79760","summary":"The protein encoded by this gene is a component of the core SMN complex, which is required for pre-mRNA splicing in the nucleus. The encoded protein is found in the nucleoplasm, in nuclear \"gems\" (Gemini of Cajal bodies), and in the cytoplasm. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":45079195,"end":45091524,"strand":1,"description":"gem nuclear organelle associated protein 7 [Source:HGNC Symbol;Acc:HGNC:20045]"}, {"versioned_ensembl_gene_id":"ENSG00000230878.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33125197,"end":33130739,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000228959.1","gene_symbol":"AL049812.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42014034,"end":42015478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274615.1","gene_symbol":"AC233968.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38078262,"end":38124770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277170.1","gene_symbol":"AC012676.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4426902,"end":4427380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201059.1","gene_symbol":"RNA5SP336","gene_name":"RNA, 5S ribosomal pseudogene 336 [Source:HGNC Symbol;Acc:HGNC:43236]","synonyms":"RN5S336","biotype":"rRNA","ncbi_id":"100873599","summary":null,"start":21000881,"end":21000997,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 336 [Source:HGNC Symbol;Acc:HGNC:43236]"}, {"versioned_ensembl_gene_id":"ENSG00000252533.1","gene_symbol":"RNU6-572P","gene_name":"RNA, U6 small nuclear 572, pseudogene [Source:HGNC Symbol;Acc:HGNC:47535]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481362","summary":null,"start":139221758,"end":139221837,"strand":1,"description":"RNA, U6 small nuclear 572, pseudogene [Source:HGNC Symbol;Acc:HGNC:47535]"}, {"versioned_ensembl_gene_id":"ENSG00000199272.1","gene_symbol":"RNU6-349P","gene_name":"RNA, U6 small nuclear 349, pseudogene [Source:HGNC Symbol;Acc:HGNC:47312]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479721","summary":null,"start":6454962,"end":6455068,"strand":1,"description":"RNA, U6 small nuclear 349, pseudogene [Source:HGNC Symbol;Acc:HGNC:47312]"}, {"versioned_ensembl_gene_id":"ENSG00000267954.2","gene_symbol":"AP000349.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23782283,"end":23783958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207117.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":159536244,"end":159536346,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273990.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":144523860,"end":144524021,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000238371.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15903669,"end":15903772,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000264202.1","gene_symbol":"SNORD48","gene_name":"small nucleolar RNA, C/D box 48 [Source:HGNC Symbol;Acc:HGNC:10188]","synonyms":"U48,RNU48,U48,RNU48","biotype":"snoRNA","ncbi_id":"26801","summary":null,"start":31822629,"end":31822691,"strand":1,"description":"small nucleolar RNA, C/D box 48 [Source:HGNC Symbol;Acc:HGNC:10188]"}, {"versioned_ensembl_gene_id":"ENSG00000263734.1","gene_symbol":"MIR4643","gene_name":"microRNA 4643 [Source:HGNC Symbol;Acc:HGNC:41814]","synonyms":"hsa-mir-4643","biotype":"miRNA","ncbi_id":"100616174","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91521660,"end":91521737,"strand":1,"description":"microRNA 4643 [Source:HGNC Symbol;Acc:HGNC:41814]"}, {"versioned_ensembl_gene_id":"ENSG00000283419.1","gene_symbol":"MIR6874","gene_name":"microRNA 6874 [Source:HGNC Symbol;Acc:HGNC:50146]","synonyms":"hsa-mir-6874","biotype":"miRNA","ncbi_id":"102466203","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5711840,"end":5711910,"strand":-1,"description":"microRNA 6874 [Source:HGNC Symbol;Acc:HGNC:50146]"}, {"versioned_ensembl_gene_id":"ENSG00000284028.1","gene_symbol":"MIR4468","gene_name":"microRNA 4468 [Source:HGNC Symbol;Acc:HGNC:41533]","synonyms":"hsa-mir-4468","biotype":"miRNA","ncbi_id":"100616226","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":138123758,"end":138123821,"strand":1,"description":"microRNA 4468 [Source:HGNC Symbol;Acc:HGNC:41533]"}, {"versioned_ensembl_gene_id":"ENSG00000206978.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":159064297,"end":159064398,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264063.1","gene_symbol":"MIR3687-2","gene_name":"microRNA 3687-2 [Source:HGNC Symbol;Acc:HGNC:50835]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504728","summary":"This record was withdrawn by miRBase.","start":8987370,"end":8987430,"strand":1,"description":"microRNA 3687-2 [Source:HGNC Symbol;Acc:HGNC:50835]"}, {"versioned_ensembl_gene_id":"ENSG00000200089.1","gene_symbol":"SNORD114-31","gene_name":"small nucleolar RNA, C/D box 114-31 [Source:HGNC Symbol;Acc:HGNC:33019]","synonyms":"14q(II-31)","biotype":"snoRNA","ncbi_id":"767612","summary":null,"start":100993236,"end":100993310,"strand":1,"description":"small nucleolar RNA, C/D box 114-31 [Source:HGNC Symbol;Acc:HGNC:33019]"}, {"versioned_ensembl_gene_id":"ENSG00000251753.1","gene_symbol":"RNU6-75P","gene_name":"RNA, U6 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:42565]","synonyms":"RNU6-75","biotype":"snRNA","ncbi_id":"100873776","summary":null,"start":90781766,"end":90781869,"strand":-1,"description":"RNA, U6 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:42565]"}, {"versioned_ensembl_gene_id":"ENSG00000273750.1","gene_symbol":"HOXB13-AS1_1","gene_name":"HOXB13 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02132]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48723188,"end":48723314,"strand":1,"description":"HOXB13 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02132]"}, {"versioned_ensembl_gene_id":"ENSG00000264941.1","gene_symbol":"MIR4474","gene_name":"microRNA 4474 [Source:HGNC Symbol;Acc:HGNC:41821]","synonyms":"hsa-mir-4474","biotype":"miRNA","ncbi_id":"100616441","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20502265,"end":20502342,"strand":-1,"description":"microRNA 4474 [Source:HGNC Symbol;Acc:HGNC:41821]"}, {"versioned_ensembl_gene_id":"ENSG00000221710.1","gene_symbol":"MIR1298","gene_name":"microRNA 1298 [Source:HGNC Symbol;Acc:HGNC:35258]","synonyms":"MIRN1298,hsa-mir-1298","biotype":"miRNA","ncbi_id":"100302153","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114715233,"end":114715344,"strand":1,"description":"microRNA 1298 [Source:HGNC Symbol;Acc:HGNC:35258]"}, {"versioned_ensembl_gene_id":"ENSG00000212051.1","gene_symbol":"MIR320C2","gene_name":"microRNA 320c-2 [Source:HGNC Symbol;Acc:HGNC:35387]","synonyms":"hsa-mir-320c-2,MIRN320C2","biotype":"miRNA","ncbi_id":"100302195","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24321686,"end":24321735,"strand":1,"description":"microRNA 320c-2 [Source:HGNC Symbol;Acc:HGNC:35387]"}, {"versioned_ensembl_gene_id":"ENSG00000212564.1","gene_symbol":"RNU6-1326P","gene_name":"RNA, U6 small nuclear 1326, pseudogene [Source:HGNC Symbol;Acc:HGNC:48289]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481951","summary":null,"start":15614283,"end":15614389,"strand":1,"description":"RNA, U6 small nuclear 1326, pseudogene [Source:HGNC Symbol;Acc:HGNC:48289]"}, {"versioned_ensembl_gene_id":"ENSG00000222371.1","gene_symbol":"RN7SKP202","gene_name":"RNA, 7SK small nuclear pseudogene 202 [Source:HGNC Symbol;Acc:HGNC:45926]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480472","summary":null,"start":68158079,"end":68158408,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 202 [Source:HGNC Symbol;Acc:HGNC:45926]"}, {"versioned_ensembl_gene_id":"ENSG00000263945.1","gene_symbol":"MIR548Y","gene_name":"microRNA 548y [Source:HGNC Symbol;Acc:HGNC:38980]","synonyms":"hsa-mir-548y","biotype":"miRNA","ncbi_id":"100500919","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47760995,"end":47761104,"strand":-1,"description":"microRNA 548y [Source:HGNC Symbol;Acc:HGNC:38980]"}, {"versioned_ensembl_gene_id":"ENSG00000207320.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3641443,"end":3641555,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207336.1","gene_symbol":"RNU6-658P","gene_name":"RNA, U6 small nuclear 658, pseudogene [Source:HGNC Symbol;Acc:HGNC:47621]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479858","summary":null,"start":74725099,"end":74725204,"strand":-1,"description":"RNA, U6 small nuclear 658, pseudogene [Source:HGNC Symbol;Acc:HGNC:47621]"}, {"versioned_ensembl_gene_id":"ENSG00000242696.3","gene_symbol":"RN7SL40P","gene_name":"RNA, 7SL, cytoplasmic 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46056]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480483","summary":null,"start":202357076,"end":202357417,"strand":-1,"description":"RNA, 7SL, cytoplasmic 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:46056]"}, {"versioned_ensembl_gene_id":"ENSG00000252810.1","gene_symbol":"RNU6-345P","gene_name":"RNA, U6 small nuclear 345, pseudogene [Source:HGNC Symbol;Acc:HGNC:47308]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481288","summary":null,"start":101915589,"end":101915695,"strand":1,"description":"RNA, U6 small nuclear 345, pseudogene [Source:HGNC Symbol;Acc:HGNC:47308]"}, {"versioned_ensembl_gene_id":"ENSG00000252257.1","gene_symbol":"RN7SKP265","gene_name":"RNA, 7SK small nuclear pseudogene 265 [Source:HGNC Symbol;Acc:HGNC:45989]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480914","summary":null,"start":181968459,"end":181968681,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 265 [Source:HGNC Symbol;Acc:HGNC:45989]"}, {"versioned_ensembl_gene_id":"ENSG00000244402.3","gene_symbol":"RN7SL314P","gene_name":"RNA, 7SL, cytoplasmic 314, pseudogene [Source:HGNC Symbol;Acc:HGNC:46330]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481836","summary":null,"start":37297398,"end":37297689,"strand":1,"description":"RNA, 7SL, cytoplasmic 314, pseudogene [Source:HGNC Symbol;Acc:HGNC:46330]"}, {"versioned_ensembl_gene_id":"ENSG00000273778.1","gene_symbol":"MIR6765","gene_name":"microRNA 6765 [Source:HGNC Symbol;Acc:HGNC:50030]","synonyms":"hsa-mir-6765","biotype":"miRNA","ncbi_id":"102465458","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105150778,"end":105150864,"strand":-1,"description":"microRNA 6765 [Source:HGNC Symbol;Acc:HGNC:50030]"}, {"versioned_ensembl_gene_id":"ENSG00000277039.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":154821943,"end":154822258,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277626.1","gene_symbol":"WNT3","gene_name":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]","synonyms":"INT4,MGC131950,INT4,MGC138323,MGC138321,MGC138323,MGC131950,MGC138321","biotype":"protein_coding","ncbi_id":"7473","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 98% amino acid identity to mouse Wnt3 protein, and 84% to human WNT3A protein, another WNT gene product. The mouse studies show the requirement of Wnt3 in primary axis formation in the mouse. Studies of the gene expression suggest that this gene may play a key role in some cases of human breast, rectal, lung, and gastric cancer through activation of the WNT-beta-catenin-TCF signaling pathway. This gene is clustered with WNT15, another family member, in the chromosome 17q21 region. [provided by RefSeq, Jul 2008]","start":47057885,"end":47113984,"strand":-1,"description":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]"}, {"versioned_ensembl_gene_id":"ENSG00000277402.1","gene_symbol":"MIR6891","gene_name":"microRNA 6891 [Source:HGNC Symbol;Acc:HGNC:50243]","synonyms":"hsa-mir-6891","biotype":"miRNA","ncbi_id":"102465537","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31355224,"end":31355316,"strand":-1,"description":"microRNA 6891 [Source:HGNC Symbol;Acc:HGNC:50243]"}, {"versioned_ensembl_gene_id":"ENSG00000264309.1","gene_symbol":"MIR4694","gene_name":"microRNA 4694 [Source:HGNC Symbol;Acc:HGNC:41586]","synonyms":"hsa-mir-4694","biotype":"miRNA","ncbi_id":"100616426","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19760004,"end":19760083,"strand":-1,"description":"microRNA 4694 [Source:HGNC Symbol;Acc:HGNC:41586]"}, {"versioned_ensembl_gene_id":"ENSG00000265917.1","gene_symbol":"MIR3685","gene_name":"microRNA 3685 [Source:HGNC Symbol;Acc:HGNC:38886]","synonyms":"hsa-mir-3685","biotype":"miRNA","ncbi_id":"100500802","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95309923,"end":95309984,"strand":1,"description":"microRNA 3685 [Source:HGNC Symbol;Acc:HGNC:38886]"}, {"versioned_ensembl_gene_id":"ENSG00000263676.1","gene_symbol":"MIR4632","gene_name":"microRNA 4632 [Source:HGNC Symbol;Acc:HGNC:41593]","synonyms":"hsa-mir-4632","biotype":"miRNA","ncbi_id":"100616438","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12191713,"end":12191773,"strand":1,"description":"microRNA 4632 [Source:HGNC Symbol;Acc:HGNC:41593]"}, {"versioned_ensembl_gene_id":"ENSG00000212309.1","gene_symbol":"SNORD70","gene_name":"Small nucleolar RNA SNORD70 [Source:RFAM;Acc:RF00575]","synonyms":"SNORD70A,HBII-234","biotype":"snoRNA","ncbi_id":"692110","summary":null,"start":202278108,"end":202278192,"strand":1,"description":"Small nucleolar RNA SNORD70 [Source:RFAM;Acc:RF00575]"}, {"versioned_ensembl_gene_id":"ENSG00000243817.3","gene_symbol":"RN7SL189P","gene_name":"RNA, 7SL, cytoplasmic 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:46205]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480973","summary":null,"start":20963579,"end":20963867,"strand":1,"description":"RNA, 7SL, cytoplasmic 189, pseudogene [Source:HGNC Symbol;Acc:HGNC:46205]"}, {"versioned_ensembl_gene_id":"ENSG00000212447.1","gene_symbol":"SNORD90","gene_name":"small nucleolar RNA, C/D box 90 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000200156.1","gene_symbol":"RNU5B-1","gene_name":"RNA, U5B small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10212]","synonyms":"U5B1,RNU5B","biotype":"snRNA","ncbi_id":"26832","summary":null,"start":65304677,"end":65304792,"strand":1,"description":"RNA, U5B small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10212]"}, {"versioned_ensembl_gene_id":"ENSG00000277512.1","gene_symbol":"SNORD65","gene_name":"small nucleolar RNA, C/D box 65 [Source:HGNC Symbol;Acc:HGNC:32726]","synonyms":"SNORD65A,HBII-135","biotype":"snoRNA","ncbi_id":"692106","summary":null,"start":16441226,"end":16441298,"strand":1,"description":"small nucleolar RNA, C/D box 65 [Source:HGNC Symbol;Acc:HGNC:32726]"}, {"versioned_ensembl_gene_id":"ENSG00000278188.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":16141767,"end":16141872,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000275268.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":140451148,"end":140451208,"strand":1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000203876.9","gene_symbol":"ADD3-AS1","gene_name":"ADD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48682]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100505933","summary":null,"start":109940104,"end":110008381,"strand":-1,"description":"ADD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48682]"}, {"versioned_ensembl_gene_id":"ENSG00000241217.3","gene_symbol":"RN7SL809P","gene_name":"RNA, 7SL, cytoplasmic 809, pseudogene [Source:HGNC Symbol;Acc:HGNC:46825]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479516","summary":null,"start":56670450,"end":56670746,"strand":-1,"description":"RNA, 7SL, cytoplasmic 809, pseudogene [Source:HGNC Symbol;Acc:HGNC:46825]"}, {"versioned_ensembl_gene_id":"ENSG00000252710.1","gene_symbol":"RNU6-295P","gene_name":"RNA, U6 small nuclear 295, pseudogene [Source:HGNC Symbol;Acc:HGNC:47258]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481272","summary":null,"start":48307927,"end":48308030,"strand":-1,"description":"RNA, U6 small nuclear 295, pseudogene [Source:HGNC Symbol;Acc:HGNC:47258]"}, {"versioned_ensembl_gene_id":"ENSG00000240625.3","gene_symbol":"RN7SL403P","gene_name":"RNA, 7SL, cytoplasmic 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:46419]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481034","summary":null,"start":43036196,"end":43036500,"strand":-1,"description":"RNA, 7SL, cytoplasmic 403, pseudogene [Source:HGNC Symbol;Acc:HGNC:46419]"}, {"versioned_ensembl_gene_id":"ENSG00000271986.2","gene_symbol":"RN7SL827P","gene_name":"RNA, 7SL, cytoplasmic 827, pseudogene [Source:HGNC Symbol;Acc:HGNC:46843]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481762","summary":null,"start":73487590,"end":73487877,"strand":-1,"description":"RNA, 7SL, cytoplasmic 827, pseudogene [Source:HGNC Symbol;Acc:HGNC:46843]"}, {"versioned_ensembl_gene_id":"ENSG00000252466.1","gene_symbol":"MIR2115","gene_name":"microRNA 2115 [Source:HGNC Symbol;Acc:HGNC:37309]","synonyms":"hsa-mir-2115","biotype":"miRNA","ncbi_id":"100313840","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48316360,"end":48316459,"strand":-1,"description":"microRNA 2115 [Source:HGNC Symbol;Acc:HGNC:37309]"}, {"versioned_ensembl_gene_id":"ENSG00000264614.1","gene_symbol":"MIR5588","gene_name":"microRNA 5588 [Source:HGNC Symbol;Acc:HGNC:43505]","synonyms":"hsa-mir-5588","biotype":"miRNA","ncbi_id":"100847054","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":185253210,"end":185253272,"strand":-1,"description":"microRNA 5588 [Source:HGNC Symbol;Acc:HGNC:43505]"}, {"versioned_ensembl_gene_id":"ENSG00000221598.3","gene_symbol":"MIR1249","gene_name":"microRNA 1249 [Source:HGNC Symbol;Acc:HGNC:35315]","synonyms":"MIRN1249,hsa-mir-1249","biotype":"miRNA","ncbi_id":"100302149","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45200954,"end":45201019,"strand":-1,"description":"microRNA 1249 [Source:HGNC Symbol;Acc:HGNC:35315]"}, {"versioned_ensembl_gene_id":"ENSG00000221410.1","gene_symbol":"MIR1238","gene_name":"microRNA 1238 [Source:HGNC Symbol;Acc:HGNC:33933]","synonyms":"MIRN1238,hsa-mir-1238","biotype":"miRNA","ncbi_id":"100302226","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10552122,"end":10552204,"strand":1,"description":"microRNA 1238 [Source:HGNC Symbol;Acc:HGNC:33933]"}, {"versioned_ensembl_gene_id":"ENSG00000242341.3","gene_symbol":"RN7SL646P","gene_name":"RNA, 7SL, cytoplasmic 646, pseudogene [Source:HGNC Symbol;Acc:HGNC:46662]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481099","summary":null,"start":178377924,"end":178378220,"strand":1,"description":"RNA, 7SL, cytoplasmic 646, pseudogene [Source:HGNC Symbol;Acc:HGNC:46662]"}, {"versioned_ensembl_gene_id":"ENSG00000251896.1","gene_symbol":"SNORD116-27","gene_name":"small nucleolar RNA, C/D box 116-27 [Source:HGNC Symbol;Acc:HGNC:33093]","synonyms":"HBII-85-27","biotype":"snoRNA","ncbi_id":"100033439","summary":null,"start":25101575,"end":25101666,"strand":1,"description":"small nucleolar RNA, C/D box 116-27 [Source:HGNC Symbol;Acc:HGNC:33093]"}, {"versioned_ensembl_gene_id":"ENSG00000252743.1","gene_symbol":"RNU6-850P","gene_name":"RNA, U6 small nuclear 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:47813]","synonyms":"RNU6-1030P","biotype":"snRNA","ncbi_id":"106481919","summary":null,"start":31756951,"end":31757053,"strand":-1,"description":"RNA, U6 small nuclear 850, pseudogene [Source:HGNC Symbol;Acc:HGNC:47813]"}, {"versioned_ensembl_gene_id":"ENSG00000202389.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":28022330,"end":28022464,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000208797.1","gene_symbol":"SNORD73A","gene_name":"small nucleolar RNA, C/D box 73A [Source:HGNC Symbol;Acc:HGNC:10235]","synonyms":"U73a,RNU73A,RNU73","biotype":"snoRNA","ncbi_id":"8944","summary":null,"start":151103827,"end":151103891,"strand":1,"description":"small nucleolar RNA, C/D box 73A [Source:HGNC Symbol;Acc:HGNC:10235]"}, {"versioned_ensembl_gene_id":"ENSG00000244080.3","gene_symbol":"RN7SL833P","gene_name":"RNA, 7SL, cytoplasmic 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:46849]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479525","summary":null,"start":11516047,"end":11516330,"strand":-1,"description":"RNA, 7SL, cytoplasmic 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:46849]"}, {"versioned_ensembl_gene_id":"ENSG00000252404.1","gene_symbol":"SCARNA16","gene_name":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]","synonyms":"ACA47","biotype":"scaRNA","ncbi_id":"677781","summary":null,"start":9082696,"end":9082879,"strand":1,"description":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]"}, {"versioned_ensembl_gene_id":"ENSG00000265233.1","gene_symbol":"ABBA01006766.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22056587,"end":22056755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262500.1","gene_symbol":"MAPK8IP1P1","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]","synonyms":"MAPK8IPP,PRKM8IPP","biotype":"processed_pseudogene","ncbi_id":"644253","summary":null,"start":46243606,"end":46245044,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]"}, {"versioned_ensembl_gene_id":"ENSG00000236035.2","gene_symbol":"AL513343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203656969,"end":203657760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267075.1","gene_symbol":"AC015818.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20545371,"end":20549952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284239.1","gene_symbol":"MIR1539","gene_name":"microRNA 1539 [Source:HGNC Symbol;Acc:HGNC:35383]","synonyms":"MIRN1539,hsa-mir-1539","biotype":"miRNA","ncbi_id":"100302257","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49487373,"end":49487422,"strand":1,"description":"microRNA 1539 [Source:HGNC Symbol;Acc:HGNC:35383]"}, {"versioned_ensembl_gene_id":"ENSG00000275671.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868948,"end":54869054,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283313.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":70848136,"end":70848218,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277084.1","gene_symbol":"RNU2-4P","gene_name":"RNA, U2 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10154]","synonyms":"U2/7,U2,RNU2P2","biotype":"snRNA","ncbi_id":"26853","summary":null,"start":43387226,"end":43387417,"strand":-1,"description":"RNA, U2 small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:10154]"}, {"versioned_ensembl_gene_id":"ENSG00000238447.1","gene_symbol":"RNU7-134P","gene_name":"RNA, U7 small nuclear 134 pseudogene [Source:HGNC Symbol;Acc:HGNC:45668]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480820","summary":null,"start":57685529,"end":57685592,"strand":-1,"description":"RNA, U7 small nuclear 134 pseudogene [Source:HGNC Symbol;Acc:HGNC:45668]"}, {"versioned_ensembl_gene_id":"ENSG00000244521.3","gene_symbol":"RN7SL700P","gene_name":"RNA, 7SL, cytoplasmic 700, pseudogene [Source:HGNC Symbol;Acc:HGNC:46716]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479478","summary":null,"start":47458941,"end":47459234,"strand":-1,"description":"RNA, 7SL, cytoplasmic 700, pseudogene [Source:HGNC Symbol;Acc:HGNC:46716]"}, {"versioned_ensembl_gene_id":"ENSG00000221420.2","gene_symbol":"SNORA81","gene_name":"small nucleolar RNA, H/ACA box 81 [Source:HGNC Symbol;Acc:HGNC:32667]","synonyms":"HBI-61","biotype":"snoRNA","ncbi_id":"677847","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA81, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":186786675,"end":186786852,"strand":1,"description":"small nucleolar RNA, H/ACA box 81 [Source:HGNC Symbol;Acc:HGNC:32667]"}, {"versioned_ensembl_gene_id":"ENSG00000252113.2","gene_symbol":"RNU6-523P","gene_name":"RNA, U6 small nuclear 523, pseudogene [Source:HGNC Symbol;Acc:HGNC:47486]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479798","summary":null,"start":67858818,"end":67858871,"strand":-1,"description":"RNA, U6 small nuclear 523, pseudogene [Source:HGNC Symbol;Acc:HGNC:47486]"}, {"versioned_ensembl_gene_id":"ENSG00000266712.3","gene_symbol":"MIR3149","gene_name":"microRNA 3149 [Source:HGNC Symbol;Acc:HGNC:38251]","synonyms":"hsa-mir-3149","biotype":"miRNA","ncbi_id":"100422921","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76966768,"end":76966850,"strand":-1,"description":"microRNA 3149 [Source:HGNC Symbol;Acc:HGNC:38251]"}, {"versioned_ensembl_gene_id":"ENSG00000222244.1","gene_symbol":"RNA5SP431","gene_name":"RNA, 5S ribosomal pseudogene 431 [Source:HGNC Symbol;Acc:HGNC:43331]","synonyms":"RN5S431","biotype":"rRNA","ncbi_id":"100873681","summary":null,"start":79264454,"end":79264573,"strand":1,"description":"RNA, 5S ribosomal pseudogene 431 [Source:HGNC Symbol;Acc:HGNC:43331]"}, {"versioned_ensembl_gene_id":"ENSG00000283193.1","gene_symbol":"MIR1243","gene_name":"microRNA 1243 [Source:HGNC Symbol;Acc:HGNC:35304]","synonyms":"MIRN1243,hsa-mir-1243","biotype":"miRNA","ncbi_id":"100302188","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113106863,"end":113106955,"strand":1,"description":"microRNA 1243 [Source:HGNC Symbol;Acc:HGNC:35304]"}, {"versioned_ensembl_gene_id":"ENSG00000252922.1","gene_symbol":"RNU6-365P","gene_name":"RNA, U6 small nuclear 365, pseudogene [Source:HGNC Symbol;Acc:HGNC:47328]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479728","summary":null,"start":41122907,"end":41123012,"strand":-1,"description":"RNA, U6 small nuclear 365, pseudogene [Source:HGNC Symbol;Acc:HGNC:47328]"}, {"versioned_ensembl_gene_id":"ENSG00000265734.1","gene_symbol":"MIR4438","gene_name":"microRNA 4438 [Source:HGNC Symbol;Acc:HGNC:41555]","synonyms":"hsa-mir-4438","biotype":"miRNA","ncbi_id":"100616375","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":213758067,"end":213758159,"strand":1,"description":"microRNA 4438 [Source:HGNC Symbol;Acc:HGNC:41555]"}, {"versioned_ensembl_gene_id":"ENSG00000186566.12","gene_symbol":"GPATCH8","gene_name":"G-patch domain containing 8 [Source:HGNC Symbol;Acc:HGNC:29066]","synonyms":"KIAA0553,GPATC8","biotype":"protein_coding","ncbi_id":"23131","summary":"The protein encoded by this gene contains an RNA-processing domain, a zinc finger domain, a lysine-rich region and a serine-rich region. A mutation in the serine-rich region of the protein is thought to be associated with hyperuricemia (PMID: 21594610). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]","start":44395284,"end":44503430,"strand":-1,"description":"G-patch domain containing 8 [Source:HGNC Symbol;Acc:HGNC:29066]"}, {"versioned_ensembl_gene_id":"ENSG00000267211.1","gene_symbol":"AC003043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44328613,"end":44331462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232386.9","gene_symbol":"AC015712.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100849561,"end":100861756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263641.1","gene_symbol":"MIR4777","gene_name":"microRNA 4777 [Source:HGNC Symbol;Acc:HGNC:41773]","synonyms":"hsa-mir-4777","biotype":"miRNA","ncbi_id":"100616317","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":231362708,"end":231362793,"strand":1,"description":"microRNA 4777 [Source:HGNC Symbol;Acc:HGNC:41773]"}, {"versioned_ensembl_gene_id":"ENSG00000275924.1","gene_symbol":"MIR6807","gene_name":"microRNA 6807 [Source:HGNC Symbol;Acc:HGNC:50191]","synonyms":"hsa-mir-6807","biotype":"miRNA","ncbi_id":"102465976","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58550285,"end":58550376,"strand":1,"description":"microRNA 6807 [Source:HGNC Symbol;Acc:HGNC:50191]"}, {"versioned_ensembl_gene_id":"ENSG00000266132.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29582168,"end":29582251,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000201820.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51253933,"end":51254023,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276784.1","gene_symbol":"JPX_2","gene_name":"JPX transcript, XIST activator conserved region 2 [Source:RFAM;Acc:RF02125]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73944595,"end":73944663,"strand":1,"description":"JPX transcript, XIST activator conserved region 2 [Source:RFAM;Acc:RF02125]"}, {"versioned_ensembl_gene_id":"ENSG00000238622.1","gene_symbol":"SNORD97","gene_name":"small nucleolar RNA, C/D box 97 [Source:HGNC Symbol;Acc:HGNC:32760]","synonyms":"U97","biotype":"snoRNA","ncbi_id":"692223","summary":null,"start":10801467,"end":10801608,"strand":-1,"description":"small nucleolar RNA, C/D box 97 [Source:HGNC Symbol;Acc:HGNC:32760]"}, {"versioned_ensembl_gene_id":"ENSG00000238650.1","gene_symbol":"SNORD54","gene_name":"small nucleolar RNA, C/D box 54 [Source:HGNC Symbol;Acc:HGNC:10204]","synonyms":"U54,RNU54","biotype":"snoRNA","ncbi_id":"26795","summary":null,"start":56073835,"end":56073901,"strand":-1,"description":"small nucleolar RNA, C/D box 54 [Source:HGNC Symbol;Acc:HGNC:10204]"}, {"versioned_ensembl_gene_id":"ENSG00000206714.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78317036,"end":78317137,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201426.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":110727021,"end":110727121,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252870.1","gene_symbol":"ACA59","gene_name":"Small nucleolar RNA ACA59 [Source:RFAM;Acc:RF01293]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":115128218,"end":115128373,"strand":-1,"description":"Small nucleolar RNA ACA59 [Source:RFAM;Acc:RF01293]"}, {"versioned_ensembl_gene_id":"ENSG00000252585.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27752874,"end":27752986,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275666.1","gene_symbol":"KCNQ1OT1_1","gene_name":"KCNQ1 overlapping transcript 1 conserved region 1 [Source:RFAM;Acc:RF01946]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2652099,"end":2652562,"strand":1,"description":"KCNQ1 overlapping transcript 1 conserved region 1 [Source:RFAM;Acc:RF01946]"}, {"versioned_ensembl_gene_id":"ENSG00000274700.1","gene_symbol":"AC091304.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28315693,"end":28315770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275648.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30731838,"end":30731970,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000173227.13","gene_symbol":"SYT12","gene_name":"synaptotagmin 12 [Source:HGNC Symbol;Acc:HGNC:18381]","synonyms":"SRG1","biotype":"protein_coding","ncbi_id":"91683","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells. Alternative splicing results in multiple transcript variants. The gene has previously been referred to as synaptotagmin XI but has been renamed synaptotagmin XII to be standard with mouse and rat official nomenclature.[provided by RefSeq, Apr 2010]","start":67006778,"end":67050863,"strand":1,"description":"synaptotagmin 12 [Source:HGNC Symbol;Acc:HGNC:18381]"}, {"versioned_ensembl_gene_id":"ENSG00000267783.1","gene_symbol":"AC022098.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14119106,"end":14119537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109046.14","gene_symbol":"WSB1","gene_name":"WD repeat and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:19221]","synonyms":"SWIP1,DKFZp564B0482,DKFZp564A122","biotype":"protein_coding","ncbi_id":"26118","summary":"This gene encodes a member of the WD-protein subfamily. This protein shares a high sequence identity to mouse and chick proteins. It contains several WD-repeats spanning most of the protein and an SOCS box in the C-terminus. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":27294076,"end":27315926,"strand":1,"description":"WD repeat and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:19221]"}, {"versioned_ensembl_gene_id":"ENSG00000259071.1","gene_symbol":"AL359397.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50326526,"end":50327909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072062.13","gene_symbol":"PRKACA","gene_name":"protein kinase cAMP-activated catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9380]","synonyms":"PKACa","biotype":"protein_coding","ncbi_id":"5566","summary":"This gene encodes one of the catalytic subunits of protein kinase A, which exists as a tetrameric holoenzyme with two regulatory subunits and two catalytic subunits, in its inactive form. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. cAMP-dependent phosphorylation of proteins by protein kinase A is important to many cellular processes, including differentiation, proliferation, and apoptosis. Constitutive activation of this gene caused either by somatic mutations, or genomic duplications of regions that include this gene, have been associated with hyperplasias and adenomas of the adrenal cortex and are linked to corticotropin-independent Cushing's syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. Tissue-specific isoforms that differ at the N-terminus have been described, and these isoforms may differ in the post-translational modifications that occur at the N-terminus of some isoforms. [provided by RefSeq, Jan 2015]","start":14091688,"end":14118084,"strand":-1,"description":"protein kinase cAMP-activated catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9380]"}, {"versioned_ensembl_gene_id":"ENSG00000264262.1","gene_symbol":"AC131274.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22676695,"end":22692618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265114.1","gene_symbol":"AC131274.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22692834,"end":22693613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243038.1","gene_symbol":"AL117692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50052857,"end":50053569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170209.4","gene_symbol":"ANKK1","gene_name":"ankyrin repeat and kinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21027]","synonyms":"X-kinase","biotype":"protein_coding","ncbi_id":"255239","summary":"The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and protein kinase superfamily involved in signal transduction pathways. This gene is closely linked to DRD2 gene (GeneID:1813) on chr 11, and a well studied restriction fragment length polymorphism (RFLP) designated TaqIA, was originally associated with the DRD2 gene, however, later was determined to be located in exon 8 of ANKK1 gene (PMIDs: 18621654, 15146457), where it causes a nonconservative amino acid substitution. It is not clear if this gene plays any role in neuropsychiatric disorders previously associated with Taq1A RFLP. [provided by RefSeq, Sep 2009]","start":113387791,"end":113400418,"strand":1,"description":"ankyrin repeat and kinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21027]"}, {"versioned_ensembl_gene_id":"ENSG00000161249.20","gene_symbol":"DMKN","gene_name":"dermokine [Source:HGNC Symbol;Acc:HGNC:25063]","synonyms":"ZD52F10","biotype":"protein_coding","ncbi_id":"93099","summary":"This gene is upregulated in inflammatory diseases, and it was first observed as expressed in the differentiated layers of skin. The most interesting aspect of this gene is the differential use of promoters and terminators to generate isoforms with unique cellular distributions and domain components. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]","start":35497220,"end":35513658,"strand":-1,"description":"dermokine [Source:HGNC Symbol;Acc:HGNC:25063]"}, {"versioned_ensembl_gene_id":"ENSG00000115568.15","gene_symbol":"ZNF142","gene_name":"zinc finger protein 142 [Source:HGNC Symbol;Acc:HGNC:12927]","synonyms":"pHZ-49,KIAA0236","biotype":"protein_coding","ncbi_id":"7701","summary":"The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]","start":218637916,"end":218659655,"strand":-1,"description":"zinc finger protein 142 [Source:HGNC Symbol;Acc:HGNC:12927]"}, {"versioned_ensembl_gene_id":"ENSG00000120256.9","gene_symbol":"LRP11","gene_name":"LDL receptor related protein 11 [Source:HGNC Symbol;Acc:HGNC:16936]","synonyms":"MANSC3,bA350J20.3","biotype":"protein_coding","ncbi_id":"84918","summary":null,"start":149818798,"end":149864026,"strand":-1,"description":"LDL receptor related protein 11 [Source:HGNC Symbol;Acc:HGNC:16936]"}, {"versioned_ensembl_gene_id":"ENSG00000120253.13","gene_symbol":"NUP43","gene_name":"nucleoporin 43 [Source:HGNC Symbol;Acc:HGNC:21182]","synonyms":"FLJ13287,bA350J20.1","biotype":"protein_coding","ncbi_id":"348995","summary":"Bidirectional transport of macromolecules between the cytoplasm and nucleus occurs through nuclear pore complexes (NPCs) embedded in the nuclear envelope. NPCs are composed of subcomplexes, and NUP43 is part of one such subcomplex, Nup107-160 (Loiodice et al., 2004 [PubMed 15146057]).[supplied by OMIM, Mar 2008]","start":149724315,"end":149749665,"strand":-1,"description":"nucleoporin 43 [Source:HGNC Symbol;Acc:HGNC:21182]"}, {"versioned_ensembl_gene_id":"ENSG00000132017.10","gene_symbol":"DCAF15","gene_name":"DDB1 and CUL4 associated factor 15 [Source:HGNC Symbol;Acc:HGNC:25095]","synonyms":"MGC99481,C19orf72","biotype":"protein_coding","ncbi_id":"90379","summary":null,"start":13952492,"end":13961449,"strand":1,"description":"DDB1 and CUL4 associated factor 15 [Source:HGNC Symbol;Acc:HGNC:25095]"}, {"versioned_ensembl_gene_id":"ENSG00000254732.1","gene_symbol":"AP001931.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57742163,"end":57793243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141552.17","gene_symbol":"ANAPC11","gene_name":"anaphase promoting complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:14452]","synonyms":"MGC882,HSPC214,Apc11p,APC11","biotype":"protein_coding","ncbi_id":"51529","summary":null,"start":81890790,"end":81900991,"strand":1,"description":"anaphase promoting complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:14452]"}, {"versioned_ensembl_gene_id":"ENSG00000231760.4","gene_symbol":"AL355312.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149796151,"end":149826294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213592.4","gene_symbol":"AP000662.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57718044,"end":57718530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260285.1","gene_symbol":"AL133367.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103525010,"end":103529072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176754.12","gene_symbol":"LINC00303","gene_name":"long intergenic non-protein coding RNA 303 [Source:HGNC Symbol;Acc:HGNC:26865]","synonyms":"NCRNA00303,FLJ40343,C1orf157","biotype":"lincRNA","ncbi_id":"284573","summary":null,"start":204032447,"end":204041265,"strand":-1,"description":"long intergenic non-protein coding RNA 303 [Source:HGNC Symbol;Acc:HGNC:26865]"}, {"versioned_ensembl_gene_id":"ENSG00000066629.16","gene_symbol":"EML1","gene_name":"echinoderm microtubule associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:3330]","synonyms":"HuEMAP,EMAPL,EMAP,ELP79","biotype":"protein_coding","ncbi_id":"2009","summary":"Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":99737693,"end":99942060,"strand":1,"description":"echinoderm microtubule associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:3330]"}, {"versioned_ensembl_gene_id":"ENSG00000236430.1","gene_symbol":"KRT8P29","gene_name":"keratin 8 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:33381]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391155","summary":null,"start":203872574,"end":203874187,"strand":-1,"description":"keratin 8 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:33381]"}, {"versioned_ensembl_gene_id":"ENSG00000182791.4","gene_symbol":"CCDC87","gene_name":"coiled-coil domain containing 87 [Source:HGNC Symbol;Acc:HGNC:25579]","synonyms":"FLJ10786","biotype":"protein_coding","ncbi_id":"55231","summary":null,"start":66590176,"end":66593083,"strand":-1,"description":"coiled-coil domain containing 87 [Source:HGNC Symbol;Acc:HGNC:25579]"}, {"versioned_ensembl_gene_id":"ENSG00000142539.9","gene_symbol":"AC020909.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50415799,"end":50428409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254996.5","gene_symbol":"ANKHD1-EIF4EBP3","gene_name":"ANKHD1-EIF4EBP3 readthrough [Source:HGNC Symbol;Acc:HGNC:33530]","synonyms":"MASK-BP3","biotype":"protein_coding","ncbi_id":"404734","summary":"The ANKHD1-EIF4EBP3 mRNA is an infrequent but naturally occurring readthrough transcript of the neighboring ANKHD1 and EIF4EBP3 genes. This readthrough transcript encodes a protein composed mostly of the multiple ankyrin repeats, single KH-domain protein, with its C-terminus encoded in a different reading frame from the shared portion of the EIF4EBP3 gene. The significance of this readthrough mRNA and the function of its protein product have not yet been determined. [provided by RefSeq, Nov 2009]","start":140401908,"end":140549569,"strand":1,"description":"ANKHD1-EIF4EBP3 readthrough [Source:HGNC Symbol;Acc:HGNC:33530]"}, {"versioned_ensembl_gene_id":"ENSG00000243056.1","gene_symbol":"EIF4EBP3","gene_name":"eukaryotic translation initiation factor 4E binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3290]","synonyms":"4E-BP3","biotype":"protein_coding","ncbi_id":"8637","summary":"This gene encodes a member of the EIF4EBP family, which consists of proteins that bind to eukaryotic translation initiation factor 4E and regulate its assembly into EIF4F, the multi-subunit translation initiation factor that recognizes the mRNA cap structure. Read-through transcription from the neighboring upstream gene (MASK or ANKHD1) generates a transcript (MASK-BP3) that encodes a protein comprised of the MASK protein sequence for the majority of the protein and a different C-terminus due to an alternate reading frame for the EIF4EBP3 segments. [provided by RefSeq, Oct 2010]","start":140547666,"end":140549578,"strand":1,"description":"eukaryotic translation initiation factor 4E binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3290]"}, {"versioned_ensembl_gene_id":"ENSG00000263731.1","gene_symbol":"AC145207.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81878425,"end":81881106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249363.1","gene_symbol":"AC011411.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145728360,"end":145729349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186314.11","gene_symbol":"PRELID2","gene_name":"PRELI domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28306]","synonyms":"MGC21644,FLJ38376","biotype":"protein_coding","ncbi_id":"153768","summary":null,"start":145471799,"end":145835369,"strand":-1,"description":"PRELI domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28306]"}, {"versioned_ensembl_gene_id":"ENSG00000232172.1","gene_symbol":"AL359092.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130651799,"end":130652383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107164.15","gene_symbol":"FUBP3","gene_name":"far upstream element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4005]","synonyms":"FBP3","biotype":"protein_coding","ncbi_id":"8939","summary":null,"start":130578965,"end":130638352,"strand":1,"description":"far upstream element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4005]"}, {"versioned_ensembl_gene_id":"ENSG00000205215.8","gene_symbol":"KRT17P7","gene_name":"keratin 17 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50725]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339258","summary":null,"start":20519312,"end":20528687,"strand":-1,"description":"keratin 17 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50725]"}, {"versioned_ensembl_gene_id":"ENSG00000259604.5","gene_symbol":"AC015712.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100861843,"end":100874369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226137.5","gene_symbol":"BAIAP2-AS1","gene_name":"BAIAP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44342]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440465","summary":null,"start":81029130,"end":81034881,"strand":-1,"description":"BAIAP2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44342]"}, {"versioned_ensembl_gene_id":"ENSG00000262873.1","gene_symbol":"AC127496.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81017969,"end":81020011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118420.16","gene_symbol":"UBE3D","gene_name":"ubiquitin protein ligase E3D [Source:HGNC Symbol;Acc:HGNC:21381]","synonyms":"YJR141W,UBE2CBP,H10BH,DKFZp434A1520,C6orf157","biotype":"protein_coding","ncbi_id":"90025","summary":null,"start":82892398,"end":83065841,"strand":-1,"description":"ubiquitin protein ligase E3D [Source:HGNC Symbol;Acc:HGNC:21381]"}, {"versioned_ensembl_gene_id":"ENSG00000261037.1","gene_symbol":"AC010266.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6019029,"end":6022283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259861.1","gene_symbol":"AC010266.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6030035,"end":6030841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231185.6","gene_symbol":"SPRY4-AS1","gene_name":"SPRY4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53465]","synonyms":"THCAT68","biotype":"antisense_RNA","ncbi_id":"101926941","summary":null,"start":142325293,"end":142672001,"strand":1,"description":"SPRY4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53465]"}, {"versioned_ensembl_gene_id":"ENSG00000179168.14","gene_symbol":"GGN","gene_name":"gametogenetin [Source:HGNC Symbol;Acc:HGNC:18869]","synonyms":"MGC33369,FLJ35713","biotype":"protein_coding","ncbi_id":"199720","summary":"This gene is a germ cell-specific gene that encodes proteins that interact with POG (proliferation of germ cells). Alternatively spliced transcript variants of a similar mouse gene encode at least three different proteins, namely gametogenetin protein 1a, gametogenetin protein 2, and gametogenetin protein 3, which show a perinuclear, cytoplasmic, and nucleolar localization, respectively. These proteins regulate the localization of POG and may play a role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":38384265,"end":38388082,"strand":-1,"description":"gametogenetin [Source:HGNC Symbol;Acc:HGNC:18869]"}, {"versioned_ensembl_gene_id":"ENSG00000283071.1","gene_symbol":"AL161669.4","gene_name":"Homo sapiens translation initiation factor IF-2-like (LOC107984640), mRNA. [Source:RefSeq mRNA;Acc:NM_001330236]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":103084210,"end":103090027,"strand":1,"description":"Homo sapiens translation initiation factor IF-2-like (LOC107984640), mRNA. [Source:RefSeq mRNA;Acc:NM_001330236]"}, {"versioned_ensembl_gene_id":"ENSG00000156587.15","gene_symbol":"UBE2L6","gene_name":"ubiquitin conjugating enzyme E2 L6 [Source:HGNC Symbol;Acc:HGNC:12490]","synonyms":"UBCH8","biotype":"protein_coding","ncbi_id":"9246","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-conjugating enzymes (E2s) and ubiquitin-protein ligases (E3s). This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is highly similar in primary structure to the enzyme encoded by the UBE2L3 gene. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":57551656,"end":57568284,"strand":-1,"description":"ubiquitin conjugating enzyme E2 L6 [Source:HGNC Symbol;Acc:HGNC:12490]"}, {"versioned_ensembl_gene_id":"ENSG00000227758.1","gene_symbol":"AL645939.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29748289,"end":29748513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104979.8","gene_symbol":"C19orf53","gene_name":"chromosome 19 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:24991]","synonyms":"LYDG10,HSPC023","biotype":"protein_coding","ncbi_id":"28974","summary":null,"start":13774168,"end":13778462,"strand":1,"description":"chromosome 19 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:24991]"}, {"versioned_ensembl_gene_id":"ENSG00000282260.1","gene_symbol":"AC019257.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1974818,"end":1975314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282334.1","gene_symbol":"KBTBD11-OT1","gene_name":"KBTBD11 overlapping transcript 1 [Source:NCBI gene;Acc:104266957]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266957","summary":null,"start":1971397,"end":1976478,"strand":1,"description":"KBTBD11 overlapping transcript 1 [Source:NCBI gene;Acc:104266957]"}, {"versioned_ensembl_gene_id":"ENSG00000186354.10","gene_symbol":"C9orf47","gene_name":"chromosome 9 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:23669]","synonyms":"FLJ37523,C9orf108,bA791O21.3","biotype":"protein_coding","ncbi_id":"286223","summary":null,"start":88990863,"end":88996140,"strand":1,"description":"chromosome 9 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:23669]"}, {"versioned_ensembl_gene_id":"ENSG00000213694.3","gene_symbol":"S1PR3","gene_name":"sphingosine-1-phosphate receptor 3 [Source:HGNC Symbol;Acc:HGNC:3167]","synonyms":"EDG3,EDG-3","biotype":"protein_coding","ncbi_id":"1903","summary":"This gene encodes a member of the EDG family of receptors, which are G protein-coupled receptors. This protein has been identified as a functional receptor for sphingosine 1-phosphate and likely contributes to the regulation of angiogenesis and vascular endothelial cell function. [provided by RefSeq, Jul 2008]","start":88991447,"end":89005010,"strand":1,"description":"sphingosine-1-phosphate receptor 3 [Source:HGNC Symbol;Acc:HGNC:3167]"}, {"versioned_ensembl_gene_id":"ENSG00000225856.2","gene_symbol":"PCNPP2","gene_name":"PEST containing nuclear protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128911","summary":null,"start":88970887,"end":88971341,"strand":-1,"description":"PEST containing nuclear protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41974]"}, {"versioned_ensembl_gene_id":"ENSG00000150773.10","gene_symbol":"PIH1D2","gene_name":"PIH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25210]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120379","summary":null,"start":112064010,"end":112074274,"strand":-1,"description":"PIH1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25210]"}, {"versioned_ensembl_gene_id":"ENSG00000005100.12","gene_symbol":"DHX33","gene_name":"DEAH-box helicase 33 [Source:HGNC Symbol;Acc:HGNC:16718]","synonyms":"FLJ21972,DKFZp762F2011,DDX33","biotype":"protein_coding","ncbi_id":"56919","summary":"This gene encodes a member of the DEAD box protein family. The DEAD box proteins are characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":5440912,"end":5469060,"strand":-1,"description":"DEAH-box helicase 33 [Source:HGNC Symbol;Acc:HGNC:16718]"}, {"versioned_ensembl_gene_id":"ENSG00000225053.1","gene_symbol":"PRPF38AP1","gene_name":"PRP38 domain containing A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44692]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389935","summary":null,"start":8161260,"end":8162192,"strand":1,"description":"PRP38 domain containing A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44692]"}, {"versioned_ensembl_gene_id":"ENSG00000176984.6","gene_symbol":"AP000679.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120168977,"end":120171679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255231.1","gene_symbol":"MRPS36P4","gene_name":"mitochondrial ribosomal protein S36 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347702","summary":null,"start":112208601,"end":112208898,"strand":1,"description":"mitochondrial ribosomal protein S36 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29774]"}, {"versioned_ensembl_gene_id":"ENSG00000243930.1","gene_symbol":"AP002884.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112218326,"end":112218720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160360.12","gene_symbol":"GPSM1","gene_name":"G protein signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:17858]","synonyms":"DKFZP727I051,AGS3","biotype":"protein_coding","ncbi_id":"26086","summary":"G-protein signaling modulators (GPSMs) play diverse functional roles through their interaction with G-protein subunits. This gene encodes a receptor-independent activator of G protein signaling, which is one of several factors that influence the basal activity of G-protein signaling systems. The protein contains seven tetratricopeptide repeats in its N-terminal half and four G-protein regulatory (GPR) motifs in its C-terminal half. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":136327476,"end":136359605,"strand":1,"description":"G protein signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:17858]"}, {"versioned_ensembl_gene_id":"ENSG00000254924.2","gene_symbol":"AP000867.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71506061,"end":71506380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225364.1","gene_symbol":"ATP6V0E1P1","gene_name":"ATPase H+ transporting V0 subunit e1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874502","summary":null,"start":132948493,"end":132948718,"strand":1,"description":"ATPase H+ transporting V0 subunit e1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41935]"}, {"versioned_ensembl_gene_id":"ENSG00000120370.12","gene_symbol":"GORAB","gene_name":"golgin, RAB6 interacting [Source:HGNC Symbol;Acc:HGNC:25676]","synonyms":"SCYL1BP1,NTKL-BP1,GO,FLJ11752","biotype":"protein_coding","ncbi_id":"92344","summary":"This gene encodes a member of the golgin family, a group of coiled-coil proteins localized to the Golgi. The encoded protein may function in the secretory pathway. The encoded protein, which also localizes to the cytoplasm, was identified by interactions with the N-terminal kinase-like protein, and thus it may function in mitosis. Mutations in this gene have been associated with geroderma osteodysplastica. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":170532129,"end":170553446,"strand":1,"description":"golgin, RAB6 interacting [Source:HGNC Symbol;Acc:HGNC:25676]"}, {"versioned_ensembl_gene_id":"ENSG00000255216.1","gene_symbol":"AP001360.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120008604,"end":120012158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131323.14","gene_symbol":"TRAF3","gene_name":"TNF receptor associated factor 3 [Source:HGNC Symbol;Acc:HGNC:12033]","synonyms":"CD40bp,CAP-1,LAP1,CRAF1","biotype":"protein_coding","ncbi_id":"7187","summary":"The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from, members of the TNF receptor (TNFR) superfamily. This protein participates in the signal transduction of CD40, a TNFR family member important for the activation of the immune response. This protein is found to be a critical component of the lymphotoxin-beta receptor (LTbetaR) signaling complex, which induces NF-kappaB activation and cell death initiated by LTbeta ligation. Epstein-Barr virus encoded latent infection membrane protein-1 (LMP1) can interact with this and several other members of the TRAF family, which may be essential for the oncogenic effects of LMP1. The protein also plays a role in the regulation of antiviral response. Mutations in this are associated with Encephalopathy, acute, infection-induced, herpes-specific 5. [provided by RefSeq, Jul 2020]","start":102777476,"end":102911500,"strand":1,"description":"TNF receptor associated factor 3 [Source:HGNC Symbol;Acc:HGNC:12033]"}, {"versioned_ensembl_gene_id":"ENSG00000225805.4","gene_symbol":"DEFB131B","gene_name":"defensin beta 131B [Source:HGNC Symbol;Acc:HGNC:38058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129216","summary":null,"start":71878453,"end":71884561,"strand":1,"description":"defensin beta 131B [Source:HGNC Symbol;Acc:HGNC:38058]"}, {"versioned_ensembl_gene_id":"ENSG00000249176.1","gene_symbol":"AC027801.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49939122,"end":49939819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255157.1","gene_symbol":"DEFB130C","gene_name":"defensin beta 130C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43843]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71856277,"end":71863658,"strand":1,"description":"defensin beta 130C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:43843]"}, {"versioned_ensembl_gene_id":"ENSG00000013561.17","gene_symbol":"RNF14","gene_name":"ring finger protein 14 [Source:HGNC Symbol;Acc:HGNC:10058]","synonyms":"TRIAD2,HFB30,ARA54","biotype":"protein_coding","ncbi_id":"9604","summary":"The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This protein interacts with androgen receptor (AR) and may function as a coactivator that induces AR target gene expression in prostate. A dominant negative mutant of this gene has been demonstrated to inhibit the AR-mediated growth of prostate cancer. This protein also interacts with class III ubiquitin-conjugating enzymes (E2s) and may act as a ubiquitin-ligase (E3) in the ubiquitination of certain nuclear proteins. Six alternatively spliced transcript variants encoding two distinct isoforms have been reported. [provided by RefSeq, Jan 2011]","start":141958328,"end":141990291,"strand":1,"description":"ring finger protein 14 [Source:HGNC Symbol;Acc:HGNC:10058]"}, {"versioned_ensembl_gene_id":"ENSG00000171604.11","gene_symbol":"CXXC5","gene_name":"CXXC finger protein 5 [Source:HGNC Symbol;Acc:HGNC:26943]","synonyms":"WID,RINF,HSPC195","biotype":"protein_coding","ncbi_id":"51523","summary":"The protein encoded by this gene is a retinoid-inducible nuclear protein containing a CXXC-type zinc finger motif. The encoded protein is involved in myelopoiesis, is required for DNA damage-induced p53 activation, regulates the differentiation of C2C12 myoblasts into myocytes, and negatively regulates cutaneous wound healing. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015]","start":139647299,"end":139683882,"strand":1,"description":"CXXC finger protein 5 [Source:HGNC Symbol;Acc:HGNC:26943]"}, {"versioned_ensembl_gene_id":"ENSG00000283648.1","gene_symbol":"AC006974.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148543677,"end":148572177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254561.3","gene_symbol":"AP003393.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119608423,"end":119659284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177910.7","gene_symbol":"SPATA31C2","gene_name":"SPATA31 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:24508]","synonyms":"FAM75C2,DKFZP434M131","biotype":"unprocessed_pseudogene","ncbi_id":"645961","summary":null,"start":88129458,"end":88138446,"strand":-1,"description":"SPATA31 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:24508]"}, {"versioned_ensembl_gene_id":"ENSG00000217878.2","gene_symbol":"AL136100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165117195,"end":165117524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160145.15","gene_symbol":"KALRN","gene_name":"kalirin RhoGEF kinase [Source:HGNC Symbol;Acc:HGNC:4814]","synonyms":"duo,DUET,ARHGEF24,TRAD,Kalirin,Hs.8004,HAPIP","biotype":"protein_coding","ncbi_id":"8997","summary":"Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]","start":124080023,"end":124726325,"strand":1,"description":"kalirin RhoGEF kinase [Source:HGNC Symbol;Acc:HGNC:4814]"}, {"versioned_ensembl_gene_id":"ENSG00000230627.1","gene_symbol":"Z97205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164108620,"end":164109694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203740.3","gene_symbol":"METTL11B","gene_name":"methyltransferase like 11B [Source:HGNC Symbol;Acc:HGNC:31932]","synonyms":"HOMT1B,C1orf184","biotype":"protein_coding","ncbi_id":"149281","summary":null,"start":170146001,"end":170167790,"strand":1,"description":"methyltransferase like 11B [Source:HGNC Symbol;Acc:HGNC:31932]"}, {"versioned_ensembl_gene_id":"ENSG00000237220.1","gene_symbol":"AC104777.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150566134,"end":150568080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255100.1","gene_symbol":"AP003119.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76782581,"end":76783062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204278.12","gene_symbol":"TMEM235","gene_name":"transmembrane protein 235 [Source:HGNC Symbol;Acc:HGNC:27563]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283999","summary":null,"start":78231310,"end":78240987,"strand":1,"description":"transmembrane protein 235 [Source:HGNC Symbol;Acc:HGNC:27563]"}, {"versioned_ensembl_gene_id":"ENSG00000235818.3","gene_symbol":"VN1R17P","gene_name":"vomeronasal 1 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:37331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441931","summary":null,"start":247236868,"end":247237957,"strand":-1,"description":"vomeronasal 1 receptor 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:37331]"}, {"versioned_ensembl_gene_id":"ENSG00000197308.9","gene_symbol":"GATA3-AS1","gene_name":"GATA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33786]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399717","summary":null,"start":8050450,"end":8053484,"strand":-1,"description":"GATA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33786]"}, {"versioned_ensembl_gene_id":"ENSG00000226659.1","gene_symbol":"AC021028.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80529597,"end":80535942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259865.1","gene_symbol":"AL390728.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":247187281,"end":247188526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145113.21","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195746765,"end":195812277,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000271423.1","gene_symbol":"CYCSP1","gene_name":"cytochrome c, somatic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20095]","synonyms":"HCP36,HC5","biotype":"processed_pseudogene","ncbi_id":"122950","summary":null,"start":76633714,"end":76634028,"strand":1,"description":"cytochrome c, somatic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20095]"}, {"versioned_ensembl_gene_id":"ENSG00000106804.7","gene_symbol":"C5","gene_name":"complement C5 [Source:HGNC Symbol;Acc:HGNC:1331]","synonyms":"CPAMD4,C5b,C5a","biotype":"protein_coding","ncbi_id":"727","summary":"This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":120952335,"end":121050276,"strand":-1,"description":"complement C5 [Source:HGNC Symbol;Acc:HGNC:1331]"}, {"versioned_ensembl_gene_id":"ENSG00000226297.1","gene_symbol":"AC007677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":229003886,"end":229004400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219487.2","gene_symbol":"AL603766.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149112009,"end":149112672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228792.2","gene_symbol":"AL356310.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":211635906,"end":211642867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078687.17","gene_symbol":"TNRC6C","gene_name":"trinucleotide repeat containing 6C [Source:HGNC Symbol;Acc:HGNC:29318]","synonyms":"KIAA1582,FLJ20015","biotype":"protein_coding","ncbi_id":"57690","summary":null,"start":77959240,"end":78108835,"strand":1,"description":"trinucleotide repeat containing 6C [Source:HGNC Symbol;Acc:HGNC:29318]"}, {"versioned_ensembl_gene_id":"ENSG00000275719.1","gene_symbol":"AC008622.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46787815,"end":46789043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255363.2","gene_symbol":"AP001189.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76607853,"end":76630427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204283.3","gene_symbol":"LINC01973","gene_name":"long intergenic non-protein coding RNA 1973 [Source:HGNC Symbol;Acc:HGNC:52800]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400624","summary":null,"start":77879027,"end":77884087,"strand":-1,"description":"long intergenic non-protein coding RNA 1973 [Source:HGNC Symbol;Acc:HGNC:52800]"}, {"versioned_ensembl_gene_id":"ENSG00000248973.1","gene_symbol":"AC106799.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4451930,"end":4866221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254605.1","gene_symbol":"AP003555.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70014858,"end":70021059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267605.5","gene_symbol":"AC016590.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37265939,"end":37271518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147862.15","gene_symbol":"NFIB","gene_name":"nuclear factor I B [Source:HGNC Symbol;Acc:HGNC:7785]","synonyms":"NFIB3,NFIB2,NFI-RED","biotype":"protein_coding","ncbi_id":"4781","summary":null,"start":14081843,"end":14398983,"strand":-1,"description":"nuclear factor I B [Source:HGNC Symbol;Acc:HGNC:7785]"}, {"versioned_ensembl_gene_id":"ENSG00000240043.1","gene_symbol":"RPS27P26","gene_name":"ribosomal protein S27 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271583","summary":null,"start":70444674,"end":70444912,"strand":-1,"description":"ribosomal protein S27 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36904]"}, {"versioned_ensembl_gene_id":"ENSG00000237478.2","gene_symbol":"AL390023.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49691262,"end":49691523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270689.1","gene_symbol":"BUD13P1","gene_name":"BUD13 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420358","summary":null,"start":95143637,"end":95145125,"strand":1,"description":"BUD13 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51560]"}, {"versioned_ensembl_gene_id":"ENSG00000256762.1","gene_symbol":"STH","gene_name":"saitohin [Source:HGNC Symbol;Acc:HGNC:18839]","synonyms":"MAPTIT","biotype":"protein_coding","ncbi_id":"246744","summary":null,"start":45999250,"end":45999694,"strand":1,"description":"saitohin [Source:HGNC Symbol;Acc:HGNC:18839]"}, {"versioned_ensembl_gene_id":"ENSG00000225779.1","gene_symbol":"AL122001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46370586,"end":46370955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123154.11","gene_symbol":"WDR83","gene_name":"WD repeat domain 83 [Source:HGNC Symbol;Acc:HGNC:32672]","synonyms":"MORG1","biotype":"protein_coding","ncbi_id":"84292","summary":"This gene encodes a member of the WD-40 protein family. The protein is proposed to function as a molecular scaffold for various multimeric protein complexes. The protein associates with several components of the extracellular signal-regulated kinase (ERK) pathway, and promotes ERK activity in response to serum or other signals. The protein also interacts with egl nine homolog 3 (EGLN3, also known as PHD3) and regulates expression of hypoxia-inducible factor 1, and has been purified as part of the spliceosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":12666800,"end":12675832,"strand":1,"description":"WD repeat domain 83 [Source:HGNC Symbol;Acc:HGNC:32672]"}, {"versioned_ensembl_gene_id":"ENSG00000264589.2","gene_symbol":"MAPT-AS1","gene_name":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128977","summary":null,"start":45799390,"end":45895630,"strand":-1,"description":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]"}, {"versioned_ensembl_gene_id":"ENSG00000233828.3","gene_symbol":"LINC01949","gene_name":"long intergenic non-protein coding RNA 1949 [Source:HGNC Symbol;Acc:HGNC:25650]","synonyms":null,"biotype":"lincRNA","ncbi_id":"55338","summary":null,"start":87205408,"end":87240145,"strand":-1,"description":"long intergenic non-protein coding RNA 1949 [Source:HGNC Symbol;Acc:HGNC:25650]"}, {"versioned_ensembl_gene_id":"ENSG00000258685.2","gene_symbol":"AL359219.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59135488,"end":59136421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236617.2","gene_symbol":"AC127070.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132887842,"end":132888583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121073.13","gene_symbol":"SLC35B1","gene_name":"solute carrier family 35 member B1 [Source:HGNC Symbol;Acc:HGNC:20798]","synonyms":"UGTREL1","biotype":"protein_coding","ncbi_id":"10237","summary":"This gene encodes a nucleotide sugar transporter which is a member of solute carrier family 35. The transporters in this family are highly conserved hydrophobic proteins with multiple transmembrane domains. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":49700943,"end":49709014,"strand":-1,"description":"solute carrier family 35 member B1 [Source:HGNC Symbol;Acc:HGNC:20798]"}, {"versioned_ensembl_gene_id":"ENSG00000224963.3","gene_symbol":"U82695.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":153479266,"end":153487088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277070.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54698377,"end":54701106,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000204652.6","gene_symbol":"RPS26P8","gene_name":"ribosomal protein S26 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644191","summary":null,"start":45608571,"end":45608918,"strand":1,"description":"ribosomal protein S26 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31329]"}, {"versioned_ensembl_gene_id":"ENSG00000168748.13","gene_symbol":"CA7","gene_name":"carbonic anhydrase 7 [Source:HGNC Symbol;Acc:HGNC:1381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"766","summary":"Carbonic anhydrases are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. The cytosolic protein encoded by this gene is predominantly expressed in the brain and contributes to bicarbonate driven GABAergic neuron excitation. Alternative splicing in the coding region results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2018]","start":66844379,"end":66854153,"strand":1,"description":"carbonic anhydrase 7 [Source:HGNC Symbol;Acc:HGNC:1381]"}, {"versioned_ensembl_gene_id":"ENSG00000136895.18","gene_symbol":"GARNL3","gene_name":"GTPase activating Rap/RanGAP domain like 3 [Source:HGNC Symbol;Acc:HGNC:25425]","synonyms":"DKFZp761J1523,bA356B19.1","biotype":"protein_coding","ncbi_id":"84253","summary":null,"start":127224265,"end":127393660,"strand":1,"description":"GTPase activating Rap/RanGAP domain like 3 [Source:HGNC Symbol;Acc:HGNC:25425]"}, {"versioned_ensembl_gene_id":"ENSG00000129657.14","gene_symbol":"SEC14L1","gene_name":"SEC14 like lipid binding 1 [Source:HGNC Symbol;Acc:HGNC:10698]","synonyms":"SEC14L,PRELID4A","biotype":"protein_coding","ncbi_id":"6397","summary":"The protein encoded by this gene belongs to the SEC14 cytosolic factor family. It has similarity to yeast SEC14 and to Japanese flying squid RALBP which suggests a possible role of the gene product in an intracellular transport system. Multiple alternatively spliced transcript variants have been found for this gene; some variants represent read-through transcripts that include exons from the upstream gene C17orf86. [provided by RefSeq, Feb 2011]","start":77086716,"end":77217101,"strand":1,"description":"SEC14 like lipid binding 1 [Source:HGNC Symbol;Acc:HGNC:10698]"}, {"versioned_ensembl_gene_id":"ENSG00000132122.11","gene_symbol":"SPATA6","gene_name":"spermatogenesis associated 6 [Source:HGNC Symbol;Acc:HGNC:18309]","synonyms":"SRF1,SRF-1,FLJ10007","biotype":"protein_coding","ncbi_id":"54558","summary":null,"start":48295372,"end":48472208,"strand":-1,"description":"spermatogenesis associated 6 [Source:HGNC Symbol;Acc:HGNC:18309]"}, {"versioned_ensembl_gene_id":"ENSG00000224986.2","gene_symbol":"PPP1R8P1","gene_name":"protein phosphatase 1 regulatory subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9297]","synonyms":"PPP1R8P","biotype":"processed_pseudogene","ncbi_id":"5512","summary":null,"start":48325080,"end":48326123,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9297]"}, {"versioned_ensembl_gene_id":"ENSG00000248363.5","gene_symbol":"AC016550.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86353803,"end":86368854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073792.15","gene_symbol":"IGF2BP2","gene_name":"insulin like growth factor 2 mRNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28867]","synonyms":"IMP-2","biotype":"protein_coding","ncbi_id":"10644","summary":"This gene encodes a protein that binds the 5' UTR of insulin-like growth factor 2 (IGF2) mRNA and regulates its translation. It plays an important role in metabolism and variation in this gene is associated with susceptibility to diabetes. Alternative splicing and promoter usage results in multiple transcript variants. Related pseudogenes are found on several chromosomes. [provided by RefSeq, Sep 2016]","start":185643739,"end":185825056,"strand":-1,"description":"insulin like growth factor 2 mRNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:28867]"}, {"versioned_ensembl_gene_id":"ENSG00000254252.1","gene_symbol":"RPL7P20","gene_name":"ribosomal protein L7 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728843","summary":null,"start":166028567,"end":166029311,"strand":-1,"description":"ribosomal protein L7 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36013]"}, {"versioned_ensembl_gene_id":"ENSG00000253946.1","gene_symbol":"AC008489.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165905126,"end":165905608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250320.5","gene_symbol":"AC113383.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84384427,"end":84490765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113430.9","gene_symbol":"IRX4","gene_name":"iroquois homeobox 4 [Source:HGNC Symbol;Acc:HGNC:6129]","synonyms":null,"biotype":"protein_coding","ncbi_id":"50805","summary":null,"start":1877413,"end":1887236,"strand":-1,"description":"iroquois homeobox 4 [Source:HGNC Symbol;Acc:HGNC:6129]"}, {"versioned_ensembl_gene_id":"ENSG00000119979.16","gene_symbol":"FAM45A","gene_name":"family with sequence similarity 45 member A [Source:HGNC Symbol;Acc:HGNC:31793]","synonyms":null,"biotype":"protein_coding","ncbi_id":"404636","summary":null,"start":119104086,"end":119137984,"strand":1,"description":"family with sequence similarity 45 member A [Source:HGNC Symbol;Acc:HGNC:31793]"}, {"versioned_ensembl_gene_id":"ENSG00000250721.1","gene_symbol":"HMGB1P22","gene_name":"high mobility group box 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644659","summary":null,"start":125265528,"end":125265651,"strand":1,"description":"high mobility group box 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39107]"}, {"versioned_ensembl_gene_id":"ENSG00000134910.12","gene_symbol":"STT3A","gene_name":"STT3A, catalytic subunit of the oligosaccharyltransferase complex [Source:HGNC Symbol;Acc:HGNC:6172]","synonyms":"TMC,STT3-A,MGC9042,ITM1","biotype":"protein_coding","ncbi_id":"3703","summary":"The protein encoded by this gene is a catalytic subunit of the N-oligosaccharyltransferase (OST) complex, which functions in the endoplasmic reticulum to transfer glycan chains to asparagine residues of target proteins. A separate complex containing a similar catalytic subunit with an overlapping function also exists. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":125591712,"end":125625215,"strand":1,"description":"STT3A, catalytic subunit of the oligosaccharyltransferase complex [Source:HGNC Symbol;Acc:HGNC:6172]"}, {"versioned_ensembl_gene_id":"ENSG00000153207.14","gene_symbol":"AHCTF1","gene_name":"AT-hook containing transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:24618]","synonyms":"ELYS","biotype":"protein_coding","ncbi_id":"25909","summary":null,"start":246839098,"end":246931978,"strand":-1,"description":"AT-hook containing transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:24618]"}, {"versioned_ensembl_gene_id":"ENSG00000105372.6","gene_symbol":"RPS19","gene_name":"ribosomal protein S19 [Source:HGNC Symbol;Acc:HGNC:10402]","synonyms":"S19,DBA","biotype":"protein_coding","ncbi_id":"6223","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":41859918,"end":41872926,"strand":1,"description":"ribosomal protein S19 [Source:HGNC Symbol;Acc:HGNC:10402]"}, {"versioned_ensembl_gene_id":"ENSG00000164620.8","gene_symbol":"RELL2","gene_name":"RELT like 2 [Source:HGNC Symbol;Acc:HGNC:26902]","synonyms":"FLJ90583,C5orf16","biotype":"protein_coding","ncbi_id":"285613","summary":null,"start":141636950,"end":141641077,"strand":1,"description":"RELT like 2 [Source:HGNC Symbol;Acc:HGNC:26902]"}, {"versioned_ensembl_gene_id":"ENSG00000254450.1","gene_symbol":"ALG9-IT1","gene_name":"ALG9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41409]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874303","summary":null,"start":111817214,"end":111829212,"strand":-1,"description":"ALG9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41409]"}, {"versioned_ensembl_gene_id":"ENSG00000188283.11","gene_symbol":"ZNF383","gene_name":"zinc finger protein 383 [Source:HGNC Symbol;Acc:HGNC:18609]","synonyms":"FLJ35863","biotype":"protein_coding","ncbi_id":"163087","summary":"The protein encoded by this gene is a KRAB-related zinc finger protein that inhibits the transcription of some MAPK signaling pathway genes. The repressor activity resides in the KRAB domain of the encoded protein. [provided by RefSeq, Sep 2016]","start":37217926,"end":37248738,"strand":1,"description":"zinc finger protein 383 [Source:HGNC Symbol;Acc:HGNC:18609]"}, {"versioned_ensembl_gene_id":"ENSG00000262855.1","gene_symbol":"AC012146.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5126740,"end":5127010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232389.1","gene_symbol":"AL583856.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70608234,"end":70609334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271967.1","gene_symbol":"AL583856.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70596438,"end":70596980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271666.1","gene_symbol":"AC008555.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34825414,"end":34825996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280167.1","gene_symbol":"AP000943.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":94559018,"end":94559374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211979.2","gene_symbol":"IGHV7-81","gene_name":"immunoglobulin heavy variable 7-81 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5669]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28378","summary":null,"start":106874583,"end":106875071,"strand":-1,"description":"immunoglobulin heavy variable 7-81 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5669]"}, {"versioned_ensembl_gene_id":"ENSG00000261754.2","gene_symbol":"AC008555.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34811589,"end":34814345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275747.1","gene_symbol":"IGHV3-79","gene_name":"immunoglobulin heavy variable 3-79 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5627]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28405","summary":null,"start":106867660,"end":106868092,"strand":-1,"description":"immunoglobulin heavy variable 3-79 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5627]"}, {"versioned_ensembl_gene_id":"ENSG00000269564.1","gene_symbol":"AC008753.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53788782,"end":53789168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228966.2","gene_symbol":"HOMER2P1","gene_name":"homer scaffolding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20336]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317768","summary":null,"start":106460092,"end":106461055,"strand":-1,"description":"homer scaffolding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20336]"}, {"versioned_ensembl_gene_id":"ENSG00000152463.14","gene_symbol":"OLAH","gene_name":"oleoyl-ACP hydrolase [Source:HGNC Symbol;Acc:HGNC:25625]","synonyms":"THEDC1,SAST,FLJ11106","biotype":"protein_coding","ncbi_id":"55301","summary":null,"start":15032227,"end":15073852,"strand":1,"description":"oleoyl-ACP hydrolase [Source:HGNC Symbol;Acc:HGNC:25625]"}, {"versioned_ensembl_gene_id":"ENSG00000272112.1","gene_symbol":"AC011374.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151724831,"end":151725356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253294.1","gene_symbol":"IGHVII-40-1","gene_name":"immunoglobulin heavy variable (II)-40-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5679]","synonyms":"IGHV(II)-40-1","biotype":"IG_V_pseudogene","ncbi_id":"28368","summary":null,"start":106440950,"end":106441007,"strand":-1,"description":"immunoglobulin heavy variable (II)-40-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5679]"}, {"versioned_ensembl_gene_id":"ENSG00000279930.1","gene_symbol":"AL032819.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1437154,"end":1439315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170145.4","gene_symbol":"SIK2","gene_name":"salt inducible kinase 2 [Source:HGNC Symbol;Acc:HGNC:21680]","synonyms":"SNF1LK2,QIK,LOH11CR1I,KIAA0781,DKFZp434K1115","biotype":"protein_coding","ncbi_id":"23235","summary":null,"start":111602391,"end":111730853,"strand":1,"description":"salt inducible kinase 2 [Source:HGNC Symbol;Acc:HGNC:21680]"}, {"versioned_ensembl_gene_id":"ENSG00000187686.4","gene_symbol":"KRT18P59","gene_name":"keratin 18 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:48886]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"399965","summary":null,"start":125113161,"end":125126781,"strand":1,"description":"keratin 18 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:48886]"}, {"versioned_ensembl_gene_id":"ENSG00000128059.8","gene_symbol":"PPAT","gene_name":"phosphoribosyl pyrophosphate amidotransferase [Source:HGNC Symbol;Acc:HGNC:9238]","synonyms":"PRAT,GPAT","biotype":"protein_coding","ncbi_id":"5471","summary":"The protein encoded by this gene is a member of the purine/pyrimidine phosphoribosyltransferase family. It is a regulatory allosteric enzyme that catalyzes the first step of de novo purine nucleotide biosythetic pathway. This gene and PAICS/AIRC gene, a bifunctional enzyme catalyzing steps six and seven of this pathway, are located in close proximity on chromosome 4, and divergently transcribed from an intergenic region. [provided by RefSeq, Mar 2011]","start":56393362,"end":56435615,"strand":-1,"description":"phosphoribosyl pyrophosphate amidotransferase [Source:HGNC Symbol;Acc:HGNC:9238]"}, {"versioned_ensembl_gene_id":"ENSG00000270302.1","gene_symbol":"AC080078.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152308283,"end":152309983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270550.1","gene_symbol":"IGHV3-30","gene_name":"immunoglobulin heavy variable 3-30 [Source:HGNC Symbol;Acc:HGNC:5591]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28439","summary":null,"start":106335082,"end":106335613,"strand":-1,"description":"immunoglobulin heavy variable 3-30 [Source:HGNC Symbol;Acc:HGNC:5591]"}, {"versioned_ensembl_gene_id":"ENSG00000116752.5","gene_symbol":"BCAS2","gene_name":"BCAS2, pre-mRNA processing factor [Source:HGNC Symbol;Acc:HGNC:975]","synonyms":"SPF27,Snt309,DAM1","biotype":"protein_coding","ncbi_id":"10286","summary":null,"start":114567557,"end":114581639,"strand":-1,"description":"BCAS2, pre-mRNA processing factor [Source:HGNC Symbol;Acc:HGNC:975]"}, {"versioned_ensembl_gene_id":"ENSG00000267615.1","gene_symbol":"AC087289.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75943832,"end":75945142,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011376.9","gene_symbol":"LARS2","gene_name":"leucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17095]","synonyms":"mtLeuRS,MGC26121,LEURS,KIAA0028","biotype":"protein_coding","ncbi_id":"23395","summary":"This gene encodes a class 1 aminoacyl-tRNA synthetase, mitochondrial leucyl-tRNA synthetase. Each of the twenty aminoacyl-tRNA synthetases catalyzes the aminoacylation of a specific tRNA or tRNA isoaccepting family with the cognate amino acid. [provided by RefSeq, Jul 2008]","start":45388506,"end":45549421,"strand":1,"description":"leucyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17095]"}, {"versioned_ensembl_gene_id":"ENSG00000122140.10","gene_symbol":"MRPS2","gene_name":"mitochondrial ribosomal protein S2 [Source:HGNC Symbol;Acc:HGNC:14495]","synonyms":"CGI-91","biotype":"protein_coding","ncbi_id":"51116","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S2 family. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2012]","start":135499984,"end":135504673,"strand":1,"description":"mitochondrial ribosomal protein S2 [Source:HGNC Symbol;Acc:HGNC:14495]"}, {"versioned_ensembl_gene_id":"ENSG00000260196.1","gene_symbol":"AC124798.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17380649,"end":17383531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196565.13","gene_symbol":"HBG2","gene_name":"hemoglobin subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:4832]","synonyms":"HBG-T1","biotype":"protein_coding","ncbi_id":"3048","summary":"The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some beta-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'- epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]","start":5253190,"end":5645789,"strand":-1,"description":"hemoglobin subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:4832]"}, {"versioned_ensembl_gene_id":"ENSG00000249123.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29739435,"end":29746663,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000274609.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54733566,"end":54744515,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000113946.3","gene_symbol":"CLDN16","gene_name":"claudin 16 [Source:HGNC Symbol;Acc:HGNC:2037]","synonyms":"PCLN1,HOMG3","biotype":"protein_coding","ncbi_id":"10686","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is found primarily in the kidneys, specifically in the thick ascending limb of Henle, where it acts as either an intercellular pore or ion concentration sensor to regulate the paracellular resorption of magnesium ions. Defects in this gene are a cause of primary hypomagnesemia, which is characterized by massive renal magnesium wasting with hypomagnesemia and hypercalciuria, resulting in nephrocalcinosis and renal failure. This gene and the CLDN1 gene are clustered on chromosome 3q28. [provided by RefSeq, Jun 2010]","start":190322541,"end":190412143,"strand":1,"description":"claudin 16 [Source:HGNC Symbol;Acc:HGNC:2037]"}, {"versioned_ensembl_gene_id":"ENSG00000248397.1","gene_symbol":"LINC00498","gene_name":"long intergenic non-protein coding RNA 498 [Source:HGNC Symbol;Acc:HGNC:43435]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377446","summary":null,"start":138298856,"end":138312658,"strand":-1,"description":"long intergenic non-protein coding RNA 498 [Source:HGNC Symbol;Acc:HGNC:43435]"}, {"versioned_ensembl_gene_id":"ENSG00000268089.2","gene_symbol":"GABRQ","gene_name":"gamma-aminobutyric acid type A receptor theta subunit [Source:HGNC Symbol;Acc:HGNC:14454]","synonyms":"THETA","biotype":"protein_coding","ncbi_id":"55879","summary":"The gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes the theta subunit of the GABA A receptor. The gene is mapped to chromosome Xq28 in a cluster of genes including those that encode the alpha 3 and epsilon subunits of the GABA A receptor. [provided by RefSeq, Jul 2017]","start":152638183,"end":152657534,"strand":1,"description":"gamma-aminobutyric acid type A receptor theta subunit [Source:HGNC Symbol;Acc:HGNC:14454]"}, {"versioned_ensembl_gene_id":"ENSG00000226963.1","gene_symbol":"AC078883.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172427774,"end":172428603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131044.16","gene_symbol":"TTLL9","gene_name":"tubulin tyrosine ligase like 9 [Source:HGNC Symbol;Acc:HGNC:16118]","synonyms":"dJ310O13.1,C20orf125","biotype":"protein_coding","ncbi_id":"164395","summary":null,"start":31870702,"end":31944963,"strand":1,"description":"tubulin tyrosine ligase like 9 [Source:HGNC Symbol;Acc:HGNC:16118]"}, {"versioned_ensembl_gene_id":"ENSG00000120458.10","gene_symbol":"MSANTD2","gene_name":"Myb/SANT DNA binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26266]","synonyms":"FLJ23342,C11orf61","biotype":"protein_coding","ncbi_id":"79684","summary":null,"start":124766498,"end":124800673,"strand":-1,"description":"Myb/SANT DNA binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26266]"}, {"versioned_ensembl_gene_id":"ENSG00000254509.1","gene_symbol":"AP000866.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124791228,"end":124791660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206268.11","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"NELF-E,RDBP,D6S45,RD,RDP","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31934274,"end":31941274,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000171790.15","gene_symbol":"SLFNL1","gene_name":"schlafen like 1 [Source:HGNC Symbol;Acc:HGNC:26313]","synonyms":"FLJ23878","biotype":"protein_coding","ncbi_id":"200172","summary":null,"start":41015597,"end":41023237,"strand":-1,"description":"schlafen like 1 [Source:HGNC Symbol;Acc:HGNC:26313]"}, {"versioned_ensembl_gene_id":"ENSG00000042832.11","gene_symbol":"TG","gene_name":"thyroglobulin [Source:HGNC Symbol;Acc:HGNC:11764]","synonyms":"TGN,AITD3","biotype":"protein_coding","ncbi_id":"7038","summary":"Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009]","start":132866958,"end":133134903,"strand":1,"description":"thyroglobulin [Source:HGNC Symbol;Acc:HGNC:11764]"}, {"versioned_ensembl_gene_id":"ENSG00000213413.2","gene_symbol":"PVRIG","gene_name":"poliovirus receptor related immunoglobulin domain containing [Source:HGNC Symbol;Acc:HGNC:32190]","synonyms":"MGC2463,C7orf15","biotype":"protein_coding","ncbi_id":"79037","summary":null,"start":100218241,"end":100221490,"strand":1,"description":"poliovirus receptor related immunoglobulin domain containing [Source:HGNC Symbol;Acc:HGNC:32190]"}, {"versioned_ensembl_gene_id":"ENSG00000256582.1","gene_symbol":"LINC02390","gene_name":"long intergenic non-protein coding RNA 2390 [Source:HGNC Symbol;Acc:HGNC:53317]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369652","summary":null,"start":9704077,"end":9709350,"strand":1,"description":"long intergenic non-protein coding RNA 2390 [Source:HGNC Symbol;Acc:HGNC:53317]"}, {"versioned_ensembl_gene_id":"ENSG00000115073.7","gene_symbol":"ACTR1B","gene_name":"ARP1 actin related protein 1 homolog B [Source:HGNC Symbol;Acc:HGNC:168]","synonyms":"CTRN2,Arp1B","biotype":"protein_coding","ncbi_id":"10120","summary":"This gene encodes a 42.3 kD subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein and is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit, like ACTR1A, is an actin-related protein. These two proteins, which are of equal length and share 90% amino acid identity, are present in a constant ratio of approximately 1:15 in the dynactin complex. [provided by RefSeq, Aug 2008]","start":97655963,"end":97664107,"strand":-1,"description":"ARP1 actin related protein 1 homolog B [Source:HGNC Symbol;Acc:HGNC:168]"}, {"versioned_ensembl_gene_id":"ENSG00000078725.12","gene_symbol":"BRINP1","gene_name":"BMP/retinoic acid inducible neural specific 1 [Source:HGNC Symbol;Acc:HGNC:2687]","synonyms":"FAM5A,DBCCR1,DBC1","biotype":"protein_coding","ncbi_id":"1620","summary":"This gene is located within a chromosomal region that shows loss of heterozygosity in some bladder cancers. It contains a 5' CpG island that may be a frequent target of hypermethylation, and it may undergo hypermethylation-based silencing in some bladder cancers. [provided by RefSeq, Jul 2008]","start":119153458,"end":119369467,"strand":-1,"description":"BMP/retinoic acid inducible neural specific 1 [Source:HGNC Symbol;Acc:HGNC:2687]"}, {"versioned_ensembl_gene_id":"ENSG00000251260.1","gene_symbol":"WDFY3-AS1","gene_name":"WDFY3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40935]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874023","summary":null,"start":84803258,"end":84810391,"strand":1,"description":"WDFY3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40935]"}, {"versioned_ensembl_gene_id":"ENSG00000108759.3","gene_symbol":"KRT32","gene_name":"keratin 32 [Source:HGNC Symbol;Acc:HGNC:6449]","synonyms":"KRTHA2,Ha-2","biotype":"protein_coding","ncbi_id":"3882","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41459811,"end":41467429,"strand":-1,"description":"keratin 32 [Source:HGNC Symbol;Acc:HGNC:6449]"}, {"versioned_ensembl_gene_id":"ENSG00000236473.1","gene_symbol":"KRT43P","gene_name":"keratin 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:48870]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418861","summary":null,"start":41448183,"end":41454055,"strand":-1,"description":"keratin 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:48870]"}, {"versioned_ensembl_gene_id":"ENSG00000279035.1","gene_symbol":"AC022211.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75130883,"end":75133043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240708.1","gene_symbol":"LINC02030","gene_name":"long intergenic non-protein coding RNA 2030 [Source:HGNC Symbol;Acc:HGNC:52864]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377098","summary":null,"start":55296200,"end":55300738,"strand":1,"description":"long intergenic non-protein coding RNA 2030 [Source:HGNC Symbol;Acc:HGNC:52864]"}, {"versioned_ensembl_gene_id":"ENSG00000227981.2","gene_symbol":"AC012668.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215579407,"end":215582635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119640.8","gene_symbol":"ACYP1","gene_name":"acylphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"97","summary":"This gene is a member of the acylphosphatase family. The encoded protein is a small cytosolic enzyme that catalyzes the hydrolysis of the carboxyl-phosphate bond of acylphosphates. Two isoenzymes have been isolated and described based on their tissue localization: erythrocyte (common) type acylphosphatase encoded by this gene, and muscle type acylphosphatase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":75053221,"end":75069483,"strand":-1,"description":"acylphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:179]"}, {"versioned_ensembl_gene_id":"ENSG00000248452.2","gene_symbol":"AC097714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26111865,"end":26113839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119630.13","gene_symbol":"PGF","gene_name":"placental growth factor [Source:HGNC Symbol;Acc:HGNC:8893]","synonyms":"SHGC-10760,PlGF-2,PLGF,PIGF,PGFL,D12S1900","biotype":"protein_coding","ncbi_id":"5228","summary":"This gene encodes a growth factor found in placenta which is homologous to vascular endothelial growth factor. Alternatively spliced transcripts encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2011]","start":74941834,"end":74955784,"strand":-1,"description":"placental growth factor [Source:HGNC Symbol;Acc:HGNC:8893]"}, {"versioned_ensembl_gene_id":"ENSG00000261650.1","gene_symbol":"AC055717.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130024493,"end":130044956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077080.9","gene_symbol":"ACTL6B","gene_name":"actin like 6B [Source:HGNC Symbol;Acc:HGNC:160]","synonyms":"BAF53B,ACTL6","biotype":"protein_coding","ncbi_id":"51412","summary":"The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene encodes a subunit of the BAF (BRG1/brm-associated factor) complex in mammals, which is functionally related to SWI/SNF complex in S. cerevisiae and Drosophila; the latter is thought to facilitate transcriptional activation of specific genes by antagonizing chromatin-mediated transcriptional repression. This subunit may be involved in the regulation of genes by structural modulation of their chromatin, specifically in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":100643097,"end":100656461,"strand":-1,"description":"actin like 6B [Source:HGNC Symbol;Acc:HGNC:160]"}, {"versioned_ensembl_gene_id":"ENSG00000225166.1","gene_symbol":"AC012462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215453707,"end":215463871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283314.1","gene_symbol":"LINC02357","gene_name":"long intergenic non-protein coding RNA 2357 [Source:HGNC Symbol;Acc:HGNC:53279]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374540","summary":null,"start":26070754,"end":26104258,"strand":1,"description":"long intergenic non-protein coding RNA 2357 [Source:HGNC Symbol;Acc:HGNC:53279]"}, {"versioned_ensembl_gene_id":"ENSG00000232724.1","gene_symbol":"TRIM80P","gene_name":"tripartite motif containing 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:51490]","synonyms":"TRIM47LP","biotype":"unitary_pseudogene","ncbi_id":"106480328","summary":null,"start":75074306,"end":75079549,"strand":1,"description":"tripartite motif containing 80, pseudogene [Source:HGNC Symbol;Acc:HGNC:51490]"}, {"versioned_ensembl_gene_id":"ENSG00000147679.11","gene_symbol":"UTP23","gene_name":"UTP23, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:28224]","synonyms":"MGC14595,C8orf53","biotype":"protein_coding","ncbi_id":"84294","summary":null,"start":116766503,"end":116849463,"strand":1,"description":"UTP23, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:28224]"}, {"versioned_ensembl_gene_id":"ENSG00000196243.5","gene_symbol":"LINC00615","gene_name":"long intergenic non-protein coding RNA 615 [Source:HGNC Symbol;Acc:HGNC:26343]","synonyms":"FLJ25378,C12orf37","biotype":"lincRNA","ncbi_id":"439916","summary":null,"start":90918023,"end":90948669,"strand":1,"description":"long intergenic non-protein coding RNA 615 [Source:HGNC Symbol;Acc:HGNC:26343]"}, {"versioned_ensembl_gene_id":"ENSG00000230121.1","gene_symbol":"AL445070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7533207,"end":7536565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228366.1","gene_symbol":"AL592437.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105710290,"end":105710781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251050.1","gene_symbol":"AC112184.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80019609,"end":80019920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214584.3","gene_symbol":"PGGT1BP2","gene_name":"protein geranylgeranyltransferase type I subunit beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45112]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132402","summary":null,"start":79892148,"end":79893175,"strand":-1,"description":"protein geranylgeranyltransferase type I subunit beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45112]"}, {"versioned_ensembl_gene_id":"ENSG00000282064.1","gene_symbol":"TRBV20-1","gene_name":"T-cell receptor beta variable 20-1 [Source:HGNC Symbol;Acc:HGNC:12196]","synonyms":"TRBV201,TCRBV2S1,TCRBV20S1","biotype":"TR_V_gene","ncbi_id":"28567","summary":null,"start":142668431,"end":142669181,"strand":1,"description":"T-cell receptor beta variable 20-1 [Source:HGNC Symbol;Acc:HGNC:12196]"}, {"versioned_ensembl_gene_id":"ENSG00000219757.1","gene_symbol":"AL357139.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102453367,"end":102453792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275390.1","gene_symbol":"AL353626.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40767870,"end":40806344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276963.1","gene_symbol":"AL353626.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40755407,"end":40767875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249055.1","gene_symbol":"TBCAP3","gene_name":"tubulin folding cofactor A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42632]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"101290501","summary":null,"start":98909537,"end":98909848,"strand":-1,"description":"tubulin folding cofactor A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42632]"}, {"versioned_ensembl_gene_id":"ENSG00000214794.4","gene_symbol":"KRT18P42","gene_name":"keratin 18 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:33412]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391819","summary":null,"start":109588338,"end":109589592,"strand":1,"description":"keratin 18 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:33412]"}, {"versioned_ensembl_gene_id":"ENSG00000276909.1","gene_symbol":"AC139494.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69767062,"end":69767356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268475.1","gene_symbol":"AC011462.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41425359,"end":41426237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234992.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"PsiGPR53,dJ271M21.8","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29538185,"end":29539268,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000238266.1","gene_symbol":"LINC00707","gene_name":"long intergenic non-protein coding RNA 707 [Source:HGNC Symbol;Acc:HGNC:44691]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507127","summary":null,"start":6779598,"end":6842906,"strand":1,"description":"long intergenic non-protein coding RNA 707 [Source:HGNC Symbol;Acc:HGNC:44691]"}, {"versioned_ensembl_gene_id":"ENSG00000197106.6","gene_symbol":"SLC6A17","gene_name":"solute carrier family 6 member 17 [Source:HGNC Symbol;Acc:HGNC:31399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388662","summary":"The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability. [provided by RefSeq, Jul 2017]","start":110150486,"end":110202202,"strand":1,"description":"solute carrier family 6 member 17 [Source:HGNC Symbol;Acc:HGNC:31399]"}, {"versioned_ensembl_gene_id":"ENSG00000235742.1","gene_symbol":"AC012308.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117023674,"end":117023851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254333.1","gene_symbol":"NDST1-AS1","gene_name":"NDST1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52899]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102546298","summary":null,"start":150475531,"end":150485968,"strand":-1,"description":"NDST1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52899]"}, {"versioned_ensembl_gene_id":"ENSG00000274157.1","gene_symbol":"AL591471.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40358454,"end":40358682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154310.16","gene_symbol":"TNIK","gene_name":"TRAF2 and NCK interacting kinase [Source:HGNC Symbol;Acc:HGNC:30765]","synonyms":"KIAA0551","biotype":"protein_coding","ncbi_id":"23043","summary":"Wnt signaling plays important roles in carcinogenesis and embryonic development. The protein encoded by this gene is a serine/threonine kinase that functions as an activator of the Wnt signaling pathway. Mutations in this gene are associated with an autosomal recessive form of cognitive disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]","start":171061339,"end":171460408,"strand":-1,"description":"TRAF2 and NCK interacting kinase [Source:HGNC Symbol;Acc:HGNC:30765]"}, {"versioned_ensembl_gene_id":"ENSG00000232433.2","gene_symbol":"GXYLT1P3","gene_name":"glucoside xylosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50422]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132541","summary":null,"start":40348599,"end":40349791,"strand":1,"description":"glucoside xylosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50422]"}, {"versioned_ensembl_gene_id":"ENSG00000257027.1","gene_symbol":"AC010186.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9658567,"end":9662085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106330.11","gene_symbol":"MOSPD3","gene_name":"motile sperm domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25078]","synonyms":"NET30,CDS3","biotype":"protein_coding","ncbi_id":"64598","summary":"This gene encodes a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality. Alternate transcriptional splice variants, encoding different isoforms, have been described. [provided by RefSeq, Jul 2008]","start":100612102,"end":100615384,"strand":1,"description":"motile sperm domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25078]"}, {"versioned_ensembl_gene_id":"ENSG00000168958.19","gene_symbol":"MFF","gene_name":"mitochondrial fission factor [Source:HGNC Symbol;Acc:HGNC:24858]","synonyms":"GL004,C2orf33","biotype":"protein_coding","ncbi_id":"56947","summary":"This is a nuclear gene encoding a protein that functions in mitochondrial and peroxisomal fission. The encoded protein recruits dynamin-1-like protein (DNM1L) to mitochondria. There are multiple pseudogenes for this gene on chromosomes 1, 5, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":227325151,"end":227357836,"strand":1,"description":"mitochondrial fission factor [Source:HGNC Symbol;Acc:HGNC:24858]"}, {"versioned_ensembl_gene_id":"ENSG00000113522.13","gene_symbol":"RAD50","gene_name":"RAD50 double strand break repair protein [Source:HGNC Symbol;Acc:HGNC:9816]","synonyms":"RAD50-2,hRad50","biotype":"protein_coding","ncbi_id":"10111","summary":"The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Rad50, a protein involved in DNA double-strand break repair. This protein forms a complex with MRE11 and NBS1. The protein complex binds to DNA and displays numerous enzymatic activities that are required for nonhomologous joining of DNA ends. This protein, cooperating with its partners, is important for DNA double-strand break repair, cell cycle checkpoint activation, telomere maintenance, and meiotic recombination. Knockout studies of the mouse homolog suggest this gene is essential for cell growth and viability. Mutations in this gene are the cause of Nijmegen breakage syndrome-like disorder.[provided by RefSeq, Apr 2010]","start":132556019,"end":132646344,"strand":1,"description":"RAD50 double strand break repair protein [Source:HGNC Symbol;Acc:HGNC:9816]"}, {"versioned_ensembl_gene_id":"ENSG00000100359.20","gene_symbol":"SGSM3","gene_name":"small G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:25228]","synonyms":"RUTBC3,RUSC3,RABGAP5,RabGAP-5,DJ1042K10.2","biotype":"protein_coding","ncbi_id":"27352","summary":null,"start":40370591,"end":40410289,"strand":1,"description":"small G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:25228]"}, {"versioned_ensembl_gene_id":"ENSG00000234413.1","gene_symbol":"AC245102.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53340986,"end":53341505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259022.2","gene_symbol":"DNAJC8P1","gene_name":"DnaJ heat shock protein family (Hsp40) member C8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319111","summary":null,"start":35430260,"end":35430631,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19928]"}, {"versioned_ensembl_gene_id":"ENSG00000267482.1","gene_symbol":"AC104996.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30059054,"end":30059147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166173.10","gene_symbol":"LARP6","gene_name":"La ribonucleoprotein domain family member 6 [Source:HGNC Symbol;Acc:HGNC:24012]","synonyms":"FLJ11196,acheron","biotype":"protein_coding","ncbi_id":"55323","summary":null,"start":70829130,"end":70854159,"strand":-1,"description":"La ribonucleoprotein domain family member 6 [Source:HGNC Symbol;Acc:HGNC:24012]"}, {"versioned_ensembl_gene_id":"ENSG00000256085.1","gene_symbol":"AC130404.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129521303,"end":129522763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236210.8","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31751793,"end":31753269,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000242797.3","gene_symbol":"GLYCTK-AS1","gene_name":"GLYCTK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41043]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874110","summary":null,"start":52288580,"end":52299067,"strand":-1,"description":"GLYCTK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41043]"}, {"versioned_ensembl_gene_id":"ENSG00000164091.11","gene_symbol":"WDR82","gene_name":"WD repeat domain 82 [Source:HGNC Symbol;Acc:HGNC:28826]","synonyms":"WDR82A,TMEM113,SWD2,PRO34047,PRO2730,MSTP107,MST107","biotype":"protein_coding","ncbi_id":"80335","summary":"TMEM113 (WDR82) is a component of the mammalian SET1A (MIM 611052)/SET1B (MIM 611055) histone H3-Lys4 methyltransferase complexes (Lee and Skalnik, 2005 [PubMed 16253997]; Lee et al., 2007 [PubMed 17355966]).[supplied by OMIM, Jul 2010]","start":52254421,"end":52288020,"strand":-1,"description":"WD repeat domain 82 [Source:HGNC Symbol;Acc:HGNC:28826]"}, {"versioned_ensembl_gene_id":"ENSG00000196511.14","gene_symbol":"TPK1","gene_name":"thiamin pyrophosphokinase 1 [Source:HGNC Symbol;Acc:HGNC:17358]","synonyms":"PP20,HTPK1","biotype":"protein_coding","ncbi_id":"27010","summary":"The protein encoded by this gene functions as a homodimer and catalyzes the conversion of thiamine to thiamine pyrophosphate, a cofactor for some enzymes of the glycolytic and energy production pathways. Defects in this gene are a cause of thiamine metabolism dysfunction syndrome-5. [provided by RefSeq, Apr 2017]","start":144451941,"end":144836395,"strand":-1,"description":"thiamin pyrophosphokinase 1 [Source:HGNC Symbol;Acc:HGNC:17358]"}, {"versioned_ensembl_gene_id":"ENSG00000235332.2","gene_symbol":"RPSAP76","gene_name":"ribosomal protein SA pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:51930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927006","summary":null,"start":125194649,"end":125195821,"strand":-1,"description":"ribosomal protein SA pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:51930]"}, {"versioned_ensembl_gene_id":"ENSG00000253561.1","gene_symbol":"AC133634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133771409,"end":133814537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262333.1","gene_symbol":"HNRNPA1P16","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440396","summary":null,"start":2306761,"end":2307715,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39134]"}, {"versioned_ensembl_gene_id":"ENSG00000213181.3","gene_symbol":"OR10N1P","gene_name":"olfactory receptor family 10 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14689]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390267","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124104965,"end":124111092,"strand":-1,"description":"olfactory receptor family 10 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14689]"}, {"versioned_ensembl_gene_id":"ENSG00000257270.1","gene_symbol":"AL928654.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105467793,"end":105470617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254067.2","gene_symbol":"AC123767.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39522976,"end":39580134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223908.5","gene_symbol":"AC068657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160023740,"end":160024045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213726.5","gene_symbol":"RPS2P52","gene_name":"ribosomal protein S2 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36059]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271250","summary":null,"start":690353,"end":691172,"strand":1,"description":"ribosomal protein S2 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36059]"}, {"versioned_ensembl_gene_id":"ENSG00000235809.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BPG309N1.15,BAT1P2","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29985328,"end":29985724,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000260366.1","gene_symbol":"AC026803.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":48926171,"end":48926444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263370.1","gene_symbol":"AC104564.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29639627,"end":29640825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251027.1","gene_symbol":"LINC01950","gene_name":"long intergenic non-protein coding RNA 1950 [Source:HGNC Symbol;Acc:HGNC:52773]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467213","summary":null,"start":106815197,"end":107011014,"strand":-1,"description":"long intergenic non-protein coding RNA 1950 [Source:HGNC Symbol;Acc:HGNC:52773]"}, {"versioned_ensembl_gene_id":"ENSG00000235125.8","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"NFKBIL,IKBL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31623212,"end":31635161,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000240531.1","gene_symbol":"AC104564.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":29716279,"end":29716685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278766.2","gene_symbol":"AC092683.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97421075,"end":97434847,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251372.5","gene_symbol":"LINC00499","gene_name":"long intergenic non-protein coding RNA 499 [Source:HGNC Symbol;Acc:HGNC:43436]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874047","summary":null,"start":138309711,"end":138424344,"strand":1,"description":"long intergenic non-protein coding RNA 499 [Source:HGNC Symbol;Acc:HGNC:43436]"}, {"versioned_ensembl_gene_id":"ENSG00000198674.3","gene_symbol":"OR10G6","gene_name":"olfactory receptor family 10 subfamily G member 6 [Source:HGNC Symbol;Acc:HGNC:14836]","synonyms":"OR10G6Q,OR10G6P","biotype":"protein_coding","ncbi_id":"79490","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123994163,"end":123995161,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 6 [Source:HGNC Symbol;Acc:HGNC:14836]"}, {"versioned_ensembl_gene_id":"ENSG00000248626.1","gene_symbol":"GAPDHP40","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:37797]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131743","summary":null,"start":159950493,"end":159951498,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:37797]"}, {"versioned_ensembl_gene_id":"ENSG00000170689.9","gene_symbol":"HOXB9","gene_name":"homeobox B9 [Source:HGNC Symbol;Acc:HGNC:5120]","synonyms":"HOX2E,HOX2","biotype":"protein_coding","ncbi_id":"3219","summary":"This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded nuclear protein functions as a sequence-specific transcription factor that is involved in cell proliferation and differentiation. Increased expression of this gene is associated with some cases of leukemia, prostate cancer and lung cancer. [provided by RefSeq, Jul 2008]","start":48621159,"end":48626356,"strand":-1,"description":"homeobox B9 [Source:HGNC Symbol;Acc:HGNC:5120]"}, {"versioned_ensembl_gene_id":"ENSG00000235697.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29900659,"end":29901025,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000225830.12","gene_symbol":"ERCC6","gene_name":"ERCC excision repair 6, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:3438]","synonyms":"RAD26,CSB,CKN2,ARMD5","biotype":"protein_coding","ncbi_id":"2074","summary":"This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]","start":49455368,"end":49539538,"strand":-1,"description":"ERCC excision repair 6, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:3438]"}, {"versioned_ensembl_gene_id":"ENSG00000212743.2","gene_symbol":"AL137145.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6350316,"end":6352762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278897.1","gene_symbol":"AC020951.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":11856032,"end":11858302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264705.1","gene_symbol":"AC090337.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69212277,"end":69214350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197503.4","gene_symbol":"LINC00477","gene_name":"long intergenic non-protein coding RNA 477 [Source:HGNC Symbol;Acc:HGNC:26557]","synonyms":"FLJ32894,FAM191B,C12orf67","biotype":"lincRNA","ncbi_id":"144360","summary":null,"start":24566964,"end":24584168,"strand":-1,"description":"long intergenic non-protein coding RNA 477 [Source:HGNC Symbol;Acc:HGNC:26557]"}, {"versioned_ensembl_gene_id":"ENSG00000079257.7","gene_symbol":"LXN","gene_name":"latexin [Source:HGNC Symbol;Acc:HGNC:13347]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56925","summary":"This gene encodes the only known protein inhibitor of zinc-dependent metallocarboxypeptidases. The encoded protein, latexin, downregulates the population size of hematopoietic stem cells. This protein is found to be downregulated in cancer cells because of promoter hypermethylation. [provided by RefSeq, Jul 2020]","start":158645822,"end":158672693,"strand":-1,"description":"latexin [Source:HGNC Symbol;Acc:HGNC:13347]"}, {"versioned_ensembl_gene_id":"ENSG00000168175.14","gene_symbol":"MAPK1IP1L","gene_name":"mitogen-activated protein kinase 1 interacting protein 1 like [Source:HGNC Symbol;Acc:HGNC:19840]","synonyms":"C14orf32","biotype":"protein_coding","ncbi_id":"93487","summary":null,"start":55051631,"end":55070192,"strand":1,"description":"mitogen-activated protein kinase 1 interacting protein 1 like [Source:HGNC Symbol;Acc:HGNC:19840]"}, {"versioned_ensembl_gene_id":"ENSG00000185591.9","gene_symbol":"SP1","gene_name":"Sp1 transcription factor [Source:HGNC Symbol;Acc:HGNC:11205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6667","summary":"The protein encoded by this gene is a zinc finger transcription factor that binds to GC-rich motifs of many promoters. The encoded protein is involved in many cellular processes, including cell differentiation, cell growth, apoptosis, immune responses, response to DNA damage, and chromatin remodeling. Post-translational modifications such as phosphorylation, acetylation, glycosylation, and proteolytic processing significantly affect the activity of this protein, which can be an activator or a repressor. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":53380176,"end":53416446,"strand":1,"description":"Sp1 transcription factor [Source:HGNC Symbol;Acc:HGNC:11205]"}, {"versioned_ensembl_gene_id":"ENSG00000123607.14","gene_symbol":"TTC21B","gene_name":"tetratricopeptide repeat domain 21B [Source:HGNC Symbol;Acc:HGNC:25660]","synonyms":"THM1,NPHP12,JBTS11,IFT139B,FLJ11457","biotype":"protein_coding","ncbi_id":"79809","summary":"This gene encodes a member of TTC21 family, containing several tetratricopeptide repeat (TPR) domains. This protein is localized to the cilium axoneme, and may play a role in retrograde intraflagellar transport in cilia. Mutations in this gene are associated with various ciliopathies, nephronophthisis 12, and asphyxiating thoracic dystrophy 4. [provided by RefSeq, Oct 2011]","start":165857475,"end":165953843,"strand":-1,"description":"tetratricopeptide repeat domain 21B [Source:HGNC Symbol;Acc:HGNC:25660]"}, {"versioned_ensembl_gene_id":"ENSG00000176951.6","gene_symbol":"OR51N1P","gene_name":"olfactory receptor family 51 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14757]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"119696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4786754,"end":4787705,"strand":1,"description":"olfactory receptor family 51 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14757]"}, {"versioned_ensembl_gene_id":"ENSG00000116133.11","gene_symbol":"DHCR24","gene_name":"24-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2859]","synonyms":"seladin-1,KIAA0018,DCE","biotype":"protein_coding","ncbi_id":"1718","summary":"This gene encodes a flavin adenine dinucleotide (FAD)-dependent oxidoreductase which catalyzes the reduction of the delta-24 double bond of sterol intermediates during cholesterol biosynthesis. The protein contains a leader sequence that directs it to the endoplasmic reticulum membrane. Missense mutations in this gene have been associated with desmosterolosis. Also, reduced expression of the gene occurs in the temporal cortex of Alzheimer disease patients and overexpression has been observed in adrenal gland cancer cells. [provided by RefSeq, Jul 2008]","start":54849633,"end":54887218,"strand":-1,"description":"24-dehydrocholesterol reductase [Source:HGNC Symbol;Acc:HGNC:2859]"}, {"versioned_ensembl_gene_id":"ENSG00000258082.1","gene_symbol":"AL391832.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234979647,"end":234980804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231904.3","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29881898,"end":29884620,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000225247.4","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"protein_coding","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29397025,"end":29398093,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000205913.6","gene_symbol":"SRRM2-AS1","gene_name":"SRRM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44162]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128788","summary":null,"start":2737076,"end":2752600,"strand":-1,"description":"SRRM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44162]"}, {"versioned_ensembl_gene_id":"ENSG00000253178.1","gene_symbol":"AC022559.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20551201,"end":20551405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251175.5","gene_symbol":"AC008243.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105746245,"end":105827172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274801.1","gene_symbol":"AC091304.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28332230,"end":28336599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238033.1","gene_symbol":"AC002480.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22649960,"end":22665533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109381.19","gene_symbol":"ELF2","gene_name":"E74 like ETS transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3317]","synonyms":"NERF,EU32,NERF-2,NERF-1B,NERF-1A","biotype":"protein_coding","ncbi_id":"1998","summary":null,"start":139028112,"end":139177218,"strand":-1,"description":"E74 like ETS transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3317]"}, {"versioned_ensembl_gene_id":"ENSG00000181450.17","gene_symbol":"ZNF678","gene_name":"zinc finger protein 678 [Source:HGNC Symbol;Acc:HGNC:28652]","synonyms":"MGC42493","biotype":"protein_coding","ncbi_id":"339500","summary":null,"start":227563543,"end":227677443,"strand":1,"description":"zinc finger protein 678 [Source:HGNC Symbol;Acc:HGNC:28652]"}, {"versioned_ensembl_gene_id":"ENSG00000103363.14","gene_symbol":"ELOB","gene_name":"elongin B [Source:HGNC Symbol;Acc:HGNC:11619]","synonyms":"TCEB2,SIII","biotype":"protein_coding","ncbi_id":"6923","summary":"This gene encodes the protein elongin B, which is a subunit of the transcription factor B (SIII) complex. The SIII complex is composed of elongins A/A2, B and C. It activates elongation by RNA polymerase II by suppressing transient pausing of the polymerase at many sites within transcription units. Elongin A functions as the transcriptionally active component of the SIII complex, whereas elongins B and C are regulatory subunits. Elongin A2 is specifically expressed in the testis, and capable of forming a stable complex with elongins B and C. The von Hippel-Lindau tumor suppressor protein binds to elongins B and C, and thereby inhibits transcription elongation. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. Pseudogenes have been identified on chromosomes 11 and 13. [provided by RefSeq, Aug 2008]","start":2771414,"end":2777297,"strand":-1,"description":"elongin B [Source:HGNC Symbol;Acc:HGNC:11619]"}, {"versioned_ensembl_gene_id":"ENSG00000278972.1","gene_symbol":"AC015920.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69433084,"end":69435533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279846.1","gene_symbol":"AC015660.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":99497812,"end":99498375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259341.1","gene_symbol":"AC015660.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99427009,"end":99431028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253584.1","gene_symbol":"AC091987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104917492,"end":105246364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250515.1","gene_symbol":"AC116353.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140732290,"end":140732863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256581.1","gene_symbol":"NLRP9P1","gene_name":"NLR family pyrin domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29888]","synonyms":"NOD25,NLRP9P","biotype":"unprocessed_pseudogene","ncbi_id":"347933","summary":null,"start":129013336,"end":129016663,"strand":1,"description":"NLR family pyrin domain containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29888]"}, {"versioned_ensembl_gene_id":"ENSG00000230404.1","gene_symbol":"AL161640.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234565298,"end":234570088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213661.3","gene_symbol":"AC106806.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121616247,"end":121616807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249600.1","gene_symbol":"AC106806.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121671373,"end":121671872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187091.13","gene_symbol":"PLCD1","gene_name":"phospholipase C delta 1 [Source:HGNC Symbol;Acc:HGNC:9060]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5333","summary":"This gene encodes a member of the phospholipase C family. Phospholipase C isozymes play critical roles in intracellular signal transduction by catalyzing the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) into the second messengers diacylglycerol (DAG) and inositol triphosphate (IP3). The encoded protein functions as a tumor suppressor in several types of cancer, and mutations in this gene are a cause of hereditary leukonychia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":38007496,"end":38029762,"strand":-1,"description":"phospholipase C delta 1 [Source:HGNC Symbol;Acc:HGNC:9060]"}, {"versioned_ensembl_gene_id":"ENSG00000249091.1","gene_symbol":"AC093903.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138277115,"end":138281784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181867.2","gene_symbol":"FTMT","gene_name":"ferritin mitochondrial [Source:HGNC Symbol;Acc:HGNC:17345]","synonyms":"MtF","biotype":"protein_coding","ncbi_id":"94033","summary":null,"start":121851955,"end":121852833,"strand":1,"description":"ferritin mitochondrial [Source:HGNC Symbol;Acc:HGNC:17345]"}, {"versioned_ensembl_gene_id":"ENSG00000148337.20","gene_symbol":"CIZ1","gene_name":"CDKN1A interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:16744]","synonyms":"ZNF356,LSFR1","biotype":"protein_coding","ncbi_id":"25792","summary":"The protein encoded by this gene is a zinc finger DNA binding protein that interacts with CIP1, part of a complex with cyclin E. The encoded protein may regulate the cellular localization of CIP1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":128166064,"end":128204383,"strand":-1,"description":"CDKN1A interacting zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:16744]"}, {"versioned_ensembl_gene_id":"ENSG00000227639.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29045035,"end":29046062,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000157765.11","gene_symbol":"SLC34A2","gene_name":"solute carrier family 34 member 2 [Source:HGNC Symbol;Acc:HGNC:11020]","synonyms":"NAPI-3B","biotype":"protein_coding","ncbi_id":"10568","summary":"The protein encoded by this gene is a pH-sensitive sodium-dependent phosphate transporter. Phosphate uptake is increased at lower pH. Defects in this gene are a cause of pulmonary alveolar microlithiasis. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":25655301,"end":25678748,"strand":1,"description":"solute carrier family 34 member 2 [Source:HGNC Symbol;Acc:HGNC:11020]"}, {"versioned_ensembl_gene_id":"ENSG00000168264.10","gene_symbol":"IRF2BP2","gene_name":"interferon regulatory factor 2 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21729]","synonyms":"IRF-2BP2","biotype":"protein_coding","ncbi_id":"359948","summary":"This gene encodes an interferon regulatory factor-2 (IRF2) binding protein that interacts with the C-terminal transcriptional repression domain of IRF2. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":234604269,"end":234609525,"strand":-1,"description":"interferon regulatory factor 2 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21729]"}, {"versioned_ensembl_gene_id":"ENSG00000177023.2","gene_symbol":"DEFB104B","gene_name":"defensin beta 104B [Source:HGNC Symbol;Acc:HGNC:26165]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503618","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 104, DEFB104A and DEFB104B, in head-to-head orientation. This gene, DEFB104B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7470308,"end":7475082,"strand":-1,"description":"defensin beta 104B [Source:HGNC Symbol;Acc:HGNC:26165]"}, {"versioned_ensembl_gene_id":"ENSG00000229246.1","gene_symbol":"LINC00377","gene_name":"long intergenic non-protein coding RNA 377 [Source:HGNC Symbol;Acc:HGNC:42703]","synonyms":"TCONS_00021861","biotype":"lincRNA","ncbi_id":"103724386","summary":null,"start":81043670,"end":81044442,"strand":1,"description":"long intergenic non-protein coding RNA 377 [Source:HGNC Symbol;Acc:HGNC:42703]"}, {"versioned_ensembl_gene_id":"ENSG00000229100.1","gene_symbol":"BX248413.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29072652,"end":29073427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231592.1","gene_symbol":"BX248413.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29077401,"end":29077996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239525.1","gene_symbol":"RPL30P5","gene_name":"ribosomal protein L30 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36302]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270978","summary":null,"start":83502699,"end":83503034,"strand":1,"description":"ribosomal protein L30 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36302]"}, {"versioned_ensembl_gene_id":"ENSG00000224939.1","gene_symbol":"LINC00184","gene_name":"long intergenic non-protein coding RNA 184 [Source:HGNC Symbol;Acc:HGNC:37192]","synonyms":"HANC,NCRNA00184","biotype":"lincRNA","ncbi_id":"100302691","summary":null,"start":234629311,"end":234634780,"strand":1,"description":"long intergenic non-protein coding RNA 184 [Source:HGNC Symbol;Acc:HGNC:37192]"}, {"versioned_ensembl_gene_id":"ENSG00000213608.5","gene_symbol":"SLC25A14P1","gene_name":"solute carrier family 25 member 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43856]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288343","summary":null,"start":83477524,"end":83478424,"strand":1,"description":"solute carrier family 25 member 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43856]"}, {"versioned_ensembl_gene_id":"ENSG00000226832.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR6-4,OR2B3P","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29087135,"end":29088141,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000249381.1","gene_symbol":"LINC00500","gene_name":"long intergenic non-protein coding RNA 500 [Source:HGNC Symbol;Acc:HGNC:43437]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106480440","summary":null,"start":138425523,"end":138436869,"strand":1,"description":"long intergenic non-protein coding RNA 500 [Source:HGNC Symbol;Acc:HGNC:43437]"}, {"versioned_ensembl_gene_id":"ENSG00000125968.8","gene_symbol":"ID1","gene_name":"inhibitor of DNA binding 1, HLH protein [Source:HGNC Symbol;Acc:HGNC:5360]","synonyms":"dJ857M17.1.2,bHLHb24","biotype":"protein_coding","ncbi_id":"3397","summary":"The protein encoded by this gene is a helix-loop-helix (HLH) protein that can form heterodimers with members of the basic HLH family of transcription factors. The encoded protein has no DNA binding activity and therefore can inhibit the DNA binding and transcriptional activation ability of basic HLH proteins with which it interacts. This protein may play a role in cell growth, senescence, and differentiation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31605283,"end":31606515,"strand":1,"description":"inhibitor of DNA binding 1, HLH protein [Source:HGNC Symbol;Acc:HGNC:5360]"}, {"versioned_ensembl_gene_id":"ENSG00000248305.1","gene_symbol":"AC105416.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138481255,"end":138482096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259440.2","gene_symbol":"NPM1P43","gene_name":"nucleophosmin 1 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:45222]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422309","summary":null,"start":73161779,"end":73162928,"strand":-1,"description":"nucleophosmin 1 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:45222]"}, {"versioned_ensembl_gene_id":"ENSG00000235632.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"hs6M1-4,OR6-5,dJ80I19.2,OR2J1P","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29101778,"end":29102716,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000248795.1","gene_symbol":"AC098859.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138560704,"end":138561941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067141.16","gene_symbol":"NEO1","gene_name":"neogenin 1 [Source:HGNC Symbol;Acc:HGNC:7754]","synonyms":"NTN1R2,NGN,IGDCC2,HsT17534","biotype":"protein_coding","ncbi_id":"4756","summary":"This gene encodes a cell surface protein that is a member of the immunoglobulin superfamily. The encoded protein consists of four N-terminal immunoglobulin-like domains, six fibronectin type III domains, a transmembrane domain and a C-terminal internal domain that shares homology with the tumor suppressor candidate gene DCC. This protein may be involved in cell growth and differentiation and in cell-cell adhesion. Defects in this gene are associated with cell proliferation in certain cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":73051710,"end":73305206,"strand":1,"description":"neogenin 1 [Source:HGNC Symbol;Acc:HGNC:7754]"}, {"versioned_ensembl_gene_id":"ENSG00000233618.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29112720,"end":29113655,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000273487.1","gene_symbol":"AC104836.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92189237,"end":92190707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250977.1","gene_symbol":"AC098859.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138664725,"end":138665569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282748.1","gene_symbol":"TRBV5-7","gene_name":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]","synonyms":"TRBV57,TCRBV5S7P,TCRBV5S7","biotype":"TR_V_gene","ncbi_id":"28608","summary":null,"start":142541804,"end":142542270,"strand":1,"description":"T-cell receptor beta variable 5-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12224]"}, {"versioned_ensembl_gene_id":"ENSG00000149428.18","gene_symbol":"HYOU1","gene_name":"hypoxia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:16931]","synonyms":"ORP150,HSP12A,Grp170","biotype":"protein_coding","ncbi_id":"10525","summary":"The protein encoded by this gene belongs to the heat shock protein 70 family. This gene uses alternative transcription start sites. A cis-acting segment found in the 5' UTR is involved in stress-dependent induction, resulting in the accumulation of this protein in the endoplasmic reticulum (ER) under hypoxic conditions. The protein encoded by this gene is thought to play an important role in protein folding and secretion in the ER. Since suppression of the protein is associated with accelerated apoptosis, it is also suggested to have an important cytoprotective role in hypoxia-induced cellular perturbation. This protein has been shown to be up-regulated in tumors, especially in breast tumors, and thus it is associated with tumor invasiveness. This gene also has an alternative translation initiation site, resulting in a protein that lacks the N-terminal signal peptide. This signal peptide-lacking protein, which is only 3 amino acids shorter than the mature protein in the ER, is thought to have a housekeeping function in the cytosol. In rat, this protein localizes to both the ER by a carboxy-terminal peptide sequence and to mitochondria by an amino-terminal targeting signal. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":119044189,"end":119057202,"strand":-1,"description":"hypoxia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:16931]"}, {"versioned_ensembl_gene_id":"ENSG00000231617.8","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"protein_coding","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33488900,"end":33499609,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000131055.4","gene_symbol":"COX4I2","gene_name":"cytochrome c oxidase subunit 4I2 [Source:HGNC Symbol;Acc:HGNC:16232]","synonyms":"dJ857M17.2,COXIV-2,COX4L2,COX4B,COX4-2","biotype":"protein_coding","ncbi_id":"84701","summary":"Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes isoform 2 of subunit IV. Isoform 1 of subunit IV is encoded by a different gene, however, the two genes show a similar structural organization. Subunit IV is the largest nuclear encoded subunit which plays a pivotal role in COX regulation. [provided by RefSeq, Jul 2008]","start":31637888,"end":31645006,"strand":1,"description":"cytochrome c oxidase subunit 4I2 [Source:HGNC Symbol;Acc:HGNC:16232]"}, {"versioned_ensembl_gene_id":"ENSG00000151304.5","gene_symbol":"SRFBP1","gene_name":"serum response factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:26333]","synonyms":"Rlb1,p49,FLJ25286,BUD22,STRAP","biotype":"protein_coding","ncbi_id":"153443","summary":null,"start":121961961,"end":122075570,"strand":1,"description":"serum response factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:26333]"}, {"versioned_ensembl_gene_id":"ENSG00000241651.4","gene_symbol":"AC099340.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128069014,"end":128069612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163125.15","gene_symbol":"RPRD2","gene_name":"regulation of nuclear pre-mRNA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29039]","synonyms":"KIAA0460,HSPC099,FLJ32145","biotype":"protein_coding","ncbi_id":"23248","summary":null,"start":150363091,"end":150476566,"strand":1,"description":"regulation of nuclear pre-mRNA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29039]"}, {"versioned_ensembl_gene_id":"ENSG00000243025.1","gene_symbol":"MTAPP1","gene_name":"methylthioadenosine phosphorylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874257","summary":null,"start":158609610,"end":158610857,"strand":-1,"description":"methylthioadenosine phosphorylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42442]"}, {"versioned_ensembl_gene_id":"ENSG00000243165.1","gene_symbol":"AC025033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158626656,"end":158626849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223945.2","gene_symbol":"AC244033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150053864,"end":150055034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100722.18","gene_symbol":"ZC3H14","gene_name":"zinc finger CCCH-type containing 14 [Source:HGNC Symbol;Acc:HGNC:20509]","synonyms":"UKp68,NY-REN-37,FLJ11806","biotype":"protein_coding","ncbi_id":"79882","summary":"The protein encoded by this gene is a poly(A)-binding protein that can affect gene expression and poly(A) tail length. The encoded protein may influence mRNA stability, nuclear export, and translation. [provided by RefSeq, May 2016]","start":88562909,"end":88627596,"strand":1,"description":"zinc finger CCCH-type containing 14 [Source:HGNC Symbol;Acc:HGNC:20509]"}, {"versioned_ensembl_gene_id":"ENSG00000277278.4","gene_symbol":"HERC2","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]","synonyms":"p528,jdf2,D15F37S1","biotype":"protein_coding","ncbi_id":"8924","summary":"This gene belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16. [provided by RefSeq, Mar 2012]","start":28320122,"end":28322152,"strand":-1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]"}, {"versioned_ensembl_gene_id":"ENSG00000163377.15","gene_symbol":"FAM19A4","gene_name":"family with sequence similarity 19 member A4, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21591]","synonyms":"TAFA-4","biotype":"protein_coding","ncbi_id":"151647","summary":"This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines, that act as regulators of immune and nervous cells. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Nov 2011]","start":68731766,"end":68953297,"strand":-1,"description":"family with sequence similarity 19 member A4, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21591]"}, {"versioned_ensembl_gene_id":"ENSG00000181396.12","gene_symbol":"OGFOD3","gene_name":"2-oxoglutarate and iron dependent oxygenase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26174]","synonyms":"FLJ22222,C17orf101","biotype":"protein_coding","ncbi_id":"79701","summary":null,"start":82389223,"end":82418637,"strand":-1,"description":"2-oxoglutarate and iron dependent oxygenase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26174]"}, {"versioned_ensembl_gene_id":"ENSG00000233119.1","gene_symbol":"BX248093.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29125038,"end":29129735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250501.2","gene_symbol":"AC093766.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138773550,"end":138801639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231670.2","gene_symbol":"BX248093.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29138704,"end":29139640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113083.13","gene_symbol":"LOX","gene_name":"lysyl oxidase [Source:HGNC Symbol;Acc:HGNC:6664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4015","summary":"This gene encodes a member of the lysyl oxidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate a regulatory propeptide and the mature enzyme. The copper-dependent amine oxidase activity of this enzyme functions in the crosslinking of collagens and elastin, while the propeptide may play a role in tumor suppression. In addition, defects in this gene have been linked with predisposition to thoracic aortic aneurysms and dissections. [provided by RefSeq, Jul 2016]","start":122063195,"end":122078360,"strand":-1,"description":"lysyl oxidase [Source:HGNC Symbol;Acc:HGNC:6664]"}, {"versioned_ensembl_gene_id":"ENSG00000233125.3","gene_symbol":"ACTBP12","gene_name":"actin, beta pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:150]","synonyms":"ACTGP5","biotype":"processed_pseudogene","ncbi_id":"100462767","summary":null,"start":92229018,"end":92229435,"strand":-1,"description":"actin, beta pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:150]"}, {"versioned_ensembl_gene_id":"ENSG00000203910.8","gene_symbol":"C1orf146","gene_name":"chromosome 1 open reading frame 146 [Source:HGNC Symbol;Acc:HGNC:24032]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388649","summary":null,"start":92217940,"end":92245813,"strand":1,"description":"chromosome 1 open reading frame 146 [Source:HGNC Symbol;Acc:HGNC:24032]"}, {"versioned_ensembl_gene_id":"ENSG00000251137.1","gene_symbol":"RPL7L1P7","gene_name":"ribosomal protein L7 like 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646641","summary":null,"start":139081654,"end":139082377,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39489]"}, {"versioned_ensembl_gene_id":"ENSG00000103507.13","gene_symbol":"BCKDK","gene_name":"branched chain ketoacid dehydrogenase kinase [Source:HGNC Symbol;Acc:HGNC:16902]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10295","summary":"The branched-chain alpha-ketoacid dehydrogenase complex (BCKD) is an important regulator of the valine, leucine, and isoleucine catabolic pathways. The protein encoded by this gene is found in the mitochondrion, where it phosphorylates and inactivates BCKD. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":31106107,"end":31112791,"strand":1,"description":"branched chain ketoacid dehydrogenase kinase [Source:HGNC Symbol;Acc:HGNC:16902]"}, {"versioned_ensembl_gene_id":"ENSG00000103740.9","gene_symbol":"ACSBG1","gene_name":"acyl-CoA synthetase bubblegum family member 1 [Source:HGNC Symbol;Acc:HGNC:29567]","synonyms":"FLJ30320,BGM,BG1,MGC14352,KIAA0631,hsBG,hBG1","biotype":"protein_coding","ncbi_id":"23205","summary":"The protein encoded by this gene possesses long-chain acyl-CoA synthetase activity. It is thought to play a central role in brain very long-chain fatty acids metabolism and myelinogenesis. [provided by RefSeq, Jul 2008]","start":78167468,"end":78245688,"strand":-1,"description":"acyl-CoA synthetase bubblegum family member 1 [Source:HGNC Symbol;Acc:HGNC:29567]"}, {"versioned_ensembl_gene_id":"ENSG00000223962.1","gene_symbol":"UBBP3","gene_name":"ubiquitin B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:12466]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"23667","summary":null,"start":148863564,"end":148863804,"strand":-1,"description":"ubiquitin B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:12466]"}, {"versioned_ensembl_gene_id":"ENSG00000205423.11","gene_symbol":"CNEP1R1","gene_name":"CTD nuclear envelope phosphatase 1 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:26759]","synonyms":"TMEM188,NEP1-R1,FLJ38101,C16orf69","biotype":"protein_coding","ncbi_id":"255919","summary":"This gene encodes a transmembrane protein that belongs to the Tmemb_18A family. A similar protein in yeast is a component of an endoplasmic reticulum-associated protein phosphatase complex and is thought to play a role in the synthesis of triacylglycerol. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":50024410,"end":50037088,"strand":1,"description":"CTD nuclear envelope phosphatase 1 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:26759]"}, {"versioned_ensembl_gene_id":"ENSG00000271525.1","gene_symbol":"ARF4P1","gene_name":"ADP ribosylation factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:657]","synonyms":"ARF4P","biotype":"processed_pseudogene","ncbi_id":"380","summary":null,"start":134078904,"end":134079444,"strand":1,"description":"ADP ribosylation factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:657]"}, {"versioned_ensembl_gene_id":"ENSG00000167136.6","gene_symbol":"ENDOG","gene_name":"endonuclease G [Source:HGNC Symbol;Acc:HGNC:3346]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2021","summary":"The protein encoded by this gene is a nuclear encoded endonuclease that is localized in the mitochondrion. The encoded protein is widely distributed among animals and cleaves DNA at GC tracts. This protein is capable of generating the RNA primers required by DNA polymerase gamma to initiate replication of mitochondrial DNA. [provided by RefSeq, Jul 2008]","start":128818474,"end":128822677,"strand":1,"description":"endonuclease G [Source:HGNC Symbol;Acc:HGNC:3346]"}, {"versioned_ensembl_gene_id":"ENSG00000196363.9","gene_symbol":"WDR5","gene_name":"WD repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:12757]","synonyms":"SWD3,CFAP89","biotype":"protein_coding","ncbi_id":"11091","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 7 WD repeats. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":134135365,"end":134159968,"strand":1,"description":"WD repeat domain 5 [Source:HGNC Symbol;Acc:HGNC:12757]"}, {"versioned_ensembl_gene_id":"ENSG00000228848.3","gene_symbol":"AC105402.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148870024,"end":148870381,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140481.14","gene_symbol":"CCDC33","gene_name":"coiled-coil domain containing 33 [Source:HGNC Symbol;Acc:HGNC:26552]","synonyms":"FLJ32855,CT61","biotype":"protein_coding","ncbi_id":"80125","summary":null,"start":74202705,"end":74336472,"strand":1,"description":"coiled-coil domain containing 33 [Source:HGNC Symbol;Acc:HGNC:26552]"}, {"versioned_ensembl_gene_id":"ENSG00000168280.16","gene_symbol":"KIF5C","gene_name":"kinesin family member 5C [Source:HGNC Symbol;Acc:HGNC:6325]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3800","summary":"The protein encoded by this gene is a kinesin heavy chain subunit involved in the transport of cargo within the central nervous system. The encoded protein, which acts as a tetramer by associating with another heavy chain and two light chains, interacts with protein kinase CK2. Mutations in this gene have been associated with complex cortical dysplasia with other brain malformations-2. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Jul 2015]","start":148875250,"end":149026759,"strand":1,"description":"kinesin family member 5C [Source:HGNC Symbol;Acc:HGNC:6325]"}, {"versioned_ensembl_gene_id":"ENSG00000198917.12","gene_symbol":"SPOUT1","gene_name":"SPOUT domain containing methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26933]","synonyms":"HSPC109,CENP-32,C9orf114","biotype":"protein_coding","ncbi_id":"51490","summary":null,"start":128819651,"end":128829821,"strand":-1,"description":"SPOUT domain containing methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26933]"}, {"versioned_ensembl_gene_id":"ENSG00000135070.14","gene_symbol":"ISCA1","gene_name":"iron-sulfur cluster assembly 1 [Source:HGNC Symbol;Acc:HGNC:28660]","synonyms":"MGC4276,ISA1,hIscA,HBLD2","biotype":"protein_coding","ncbi_id":"81689","summary":"ISCA1 is a mitochondrial protein involved in the biogenesis and assembly of iron-sulfur clusters, which play a role in electron-transfer reactions (Cozar-Castellano et al., 2004 [PubMed 15262227]).[supplied by OMIM, Mar 2008]","start":86264546,"end":86283102,"strand":-1,"description":"iron-sulfur cluster assembly 1 [Source:HGNC Symbol;Acc:HGNC:28660]"}, {"versioned_ensembl_gene_id":"ENSG00000270809.1","gene_symbol":"CHCHD2P11","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49029]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060040","summary":null,"start":42181465,"end":42181921,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49029]"}, {"versioned_ensembl_gene_id":"ENSG00000237263.1","gene_symbol":"MAPK6PS3","gene_name":"mitogen-activated protein kinase 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317684","summary":null,"start":42068932,"end":42071093,"strand":-1,"description":"mitogen-activated protein kinase 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18977]"}, {"versioned_ensembl_gene_id":"ENSG00000231530.1","gene_symbol":"AL157932.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42043727,"end":42044247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225685.1","gene_symbol":"TSPY5P","gene_name":"testis specific protein, Y-linked 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:23907]","synonyms":"TSPYP5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"379027","summary":null,"start":10066554,"end":10069151,"strand":-1,"description":"testis specific protein, Y-linked 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:23907]"}, {"versioned_ensembl_gene_id":"ENSG00000226000.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"dJ80I19.4,OR6-8,hs6M1-6","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29174136,"end":29175407,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000261204.1","gene_symbol":"AC004449.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":637105,"end":637537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278873.1","gene_symbol":"PRO1804","gene_name":"uncharacterized LOC100133319 [Source:NCBI gene;Acc:100133319]","synonyms":null,"biotype":"TEC","ncbi_id":"100133319","summary":null,"start":69232963,"end":69235012,"strand":-1,"description":"uncharacterized LOC100133319 [Source:NCBI gene;Acc:100133319]"}, {"versioned_ensembl_gene_id":"ENSG00000257718.1","gene_symbol":"AC067735.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38906451,"end":38909592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070388.11","gene_symbol":"FGF22","gene_name":"fibroblast growth factor 22 [Source:HGNC Symbol;Acc:HGNC:3679]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27006","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The mouse homolog of this gene was found to be preferentially expressed in the inner root sheath of the hair follicle, which suggested a role in hair development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":639879,"end":644371,"strand":1,"description":"fibroblast growth factor 22 [Source:HGNC Symbol;Acc:HGNC:3679]"}, {"versioned_ensembl_gene_id":"ENSG00000237046.8","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30181237,"end":30193864,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000139117.13","gene_symbol":"CPNE8","gene_name":"copine 8 [Source:HGNC Symbol;Acc:HGNC:23498]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144402","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene is one of several genes that encode a calcium-dependent protein containing two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. [provided by RefSeq, Jul 2008]","start":38646822,"end":38907430,"strand":-1,"description":"copine 8 [Source:HGNC Symbol;Acc:HGNC:23498]"}, {"versioned_ensembl_gene_id":"ENSG00000241475.1","gene_symbol":"AL160408.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234660271,"end":234667104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187082.2","gene_symbol":"DEFB106B","gene_name":"defensin beta 106B [Source:HGNC Symbol;Acc:HGNC:28879]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503841","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 106, DEFB106A and DEFB106B, in head-to-head orientation. This gene, DEFB106B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7482504,"end":7486400,"strand":-1,"description":"defensin beta 106B [Source:HGNC Symbol;Acc:HGNC:28879]"}, {"versioned_ensembl_gene_id":"ENSG00000228044.2","gene_symbol":"AL160408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234646289,"end":234683176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272362.1","gene_symbol":"AL160408.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234644666,"end":234647571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205464.11","gene_symbol":"ATP6AP1L","gene_name":"ATPase H+ transporting accessory protein 1 like [Source:HGNC Symbol;Acc:HGNC:28091]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92270","summary":null,"start":82279462,"end":82386977,"strand":1,"description":"ATPase H+ transporting accessory protein 1 like [Source:HGNC Symbol;Acc:HGNC:28091]"}, {"versioned_ensembl_gene_id":"ENSG00000230628.1","gene_symbol":"AL160408.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234669523,"end":234696153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267653.1","gene_symbol":"AC002546.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69477139,"end":69501755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234623.9","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTNL11,BTN6","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29656933,"end":29672325,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000147174.11","gene_symbol":"GCNA","gene_name":"germ cell nuclear acidic peptidase [Source:HGNC Symbol;Acc:HGNC:15805]","synonyms":"NAAR1,ACRC","biotype":"protein_coding","ncbi_id":"93953","summary":null,"start":71578411,"end":71613583,"strand":1,"description":"germ cell nuclear acidic peptidase [Source:HGNC Symbol;Acc:HGNC:15805]"}, {"versioned_ensembl_gene_id":"ENSG00000108984.13","gene_symbol":"MAP2K6","gene_name":"mitogen-activated protein kinase kinase 6 [Source:HGNC Symbol;Acc:HGNC:6846]","synonyms":"SAPKK3,PRKMK6,MKK6,MEK6,MAPKK6","biotype":"protein_coding","ncbi_id":"5608","summary":"This gene encodes a member of the dual specificity protein kinase family, which functions as a mitogen-activated protein (MAP) kinase kinase. MAP kinases, also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals. This protein phosphorylates and activates p38 MAP kinase in response to inflammatory cytokines or environmental stress. As an essential component of p38 MAP kinase mediated signal transduction pathway, this gene is involved in many cellular processes such as stress induced cell cycle arrest, transcription activation and apoptosis. [provided by RefSeq, Jul 2008]","start":69414698,"end":69543331,"strand":1,"description":"mitogen-activated protein kinase kinase 6 [Source:HGNC Symbol;Acc:HGNC:6846]"}, {"versioned_ensembl_gene_id":"ENSG00000273249.1","gene_symbol":"BX649632.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134132242,"end":134135772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269652.1","gene_symbol":"AC011510.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41221426,"end":41222051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184669.8","gene_symbol":"OR7E14P","gene_name":"olfactory receptor family 7 subfamily E member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:8385]","synonyms":"OR7E151P,OR11-5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10819","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":17013998,"end":17053024,"strand":1,"description":"olfactory receptor family 7 subfamily E member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:8385]"}, {"versioned_ensembl_gene_id":"ENSG00000251026.1","gene_symbol":"LINC02163","gene_name":"long intergenic non-protein coding RNA 2163 [Source:HGNC Symbol;Acc:HGNC:53024]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986389","summary":null,"start":104079911,"end":104105403,"strand":1,"description":"long intergenic non-protein coding RNA 2163 [Source:HGNC Symbol;Acc:HGNC:53024]"}, {"versioned_ensembl_gene_id":"ENSG00000166689.15","gene_symbol":"PLEKHA7","gene_name":"pleckstrin homology domain containing A7 [Source:HGNC Symbol;Acc:HGNC:27049]","synonyms":"DKFZp686M22243","biotype":"protein_coding","ncbi_id":"144100","summary":null,"start":16777317,"end":17014443,"strand":-1,"description":"pleckstrin homology domain containing A7 [Source:HGNC Symbol;Acc:HGNC:27049]"}, {"versioned_ensembl_gene_id":"ENSG00000248393.1","gene_symbol":"AC026782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82545862,"end":82546310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250740.1","gene_symbol":"AC109361.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105927060,"end":105932722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248870.1","gene_symbol":"AC026782.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82586776,"end":82587411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282610.1","gene_symbol":"AC233282.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142549110,"end":142549542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249100.1","gene_symbol":"AC008885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82765404,"end":82766333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231079.7","gene_symbol":"AC105402.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148866470,"end":148888823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240411.2","gene_symbol":"RPL5P16","gene_name":"ribosomal protein L5 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270837","summary":null,"start":82777797,"end":82778586,"strand":1,"description":"ribosomal protein L5 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36009]"}, {"versioned_ensembl_gene_id":"ENSG00000168743.12","gene_symbol":"NPNT","gene_name":"nephronectin [Source:HGNC Symbol;Acc:HGNC:27405]","synonyms":"POEM,EGFL6L","biotype":"protein_coding","ncbi_id":"255743","summary":null,"start":105894775,"end":106004027,"strand":1,"description":"nephronectin [Source:HGNC Symbol;Acc:HGNC:27405]"}, {"versioned_ensembl_gene_id":"ENSG00000231129.8","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"EST123147,ABC50","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30616012,"end":30641816,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000226340.1","gene_symbol":"AC105402.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148872253,"end":148872797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119689.14","gene_symbol":"DLST","gene_name":"dihydrolipoamide S-succinyltransferase [Source:HGNC Symbol;Acc:HGNC:2911]","synonyms":"DLTS","biotype":"protein_coding","ncbi_id":"1743","summary":"This gene encodes a mitochondrial protein that belongs to the 2-oxoacid dehydrogenase family. This protein is one of the three components (the E2 component) of the 2-oxoglutarate dehydrogenase complex that catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2011]","start":74881891,"end":74903745,"strand":1,"description":"dihydrolipoamide S-succinyltransferase [Source:HGNC Symbol;Acc:HGNC:2911]"}, {"versioned_ensembl_gene_id":"ENSG00000082497.11","gene_symbol":"SERTAD4","gene_name":"SERTA domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25236]","synonyms":"DJ667H12.2","biotype":"protein_coding","ncbi_id":"56256","summary":null,"start":210232799,"end":210246631,"strand":1,"description":"SERTA domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25236]"}, {"versioned_ensembl_gene_id":"ENSG00000069764.9","gene_symbol":"PLA2G10","gene_name":"phospholipase A2 group X [Source:HGNC Symbol;Acc:HGNC:9029]","synonyms":"GXPLA2","biotype":"protein_coding","ncbi_id":"8399","summary":"This gene encodes a member of the phospholipase A2 family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This calcium-dependent enzyme hydrolyzes glycerophospholipids to produce free fatty acids and lysophospholipids. In one example, this enzyme catalyzes the release of arachidonic acid from cell membrane phospholipids, thus playing a role in the production of various inflammatory lipid mediators, such as prostaglandins. The encoded protein may promote the survival of breast cancer cells through its role in lipid metabolism. [provided by RefSeq, Nov 2015]","start":14672545,"end":14694669,"strand":-1,"description":"phospholipase A2 group X [Source:HGNC Symbol;Acc:HGNC:9029]"}, {"versioned_ensembl_gene_id":"ENSG00000270344.2","gene_symbol":"POC1B-AS1","gene_name":"POC1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52949]","synonyms":"RP11-734K2.4","biotype":"antisense_RNA","ncbi_id":"109729146","summary":null,"start":89525654,"end":89548005,"strand":1,"description":"POC1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52949]"}, {"versioned_ensembl_gene_id":"ENSG00000226982.4","gene_symbol":"CENPCP1","gene_name":"centromere protein C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1855]","synonyms":"CENPC,CENPC2,CENPC1P1","biotype":"processed_pseudogene","ncbi_id":"1061","summary":null,"start":89500093,"end":89502670,"strand":1,"description":"centromere protein C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1855]"}, {"versioned_ensembl_gene_id":"ENSG00000257594.3","gene_symbol":"GALNT4","gene_name":"polypeptide N-acetylgalactosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4126]","synonyms":"GalNAc-T4","biotype":"protein_coding","ncbi_id":"8693","summary":"This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. In vitro, the encoded protein can complement other GalNAc-Ts in the complete O-glycosylation of the mucin-1 tandem repeat and can O-glycosylate the P-selectin glycoprotein ligand-1 molecule. The coding region of this gene is contained within a single exon. Fusion transcripts, which combine part of this gene with the 5' exons of the neighboring POC1B (POC1 centriolar protein homolog B) gene, also exist. [provided by RefSeq, Dec 2010]","start":89519408,"end":89524806,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:4126]"}, {"versioned_ensembl_gene_id":"ENSG00000259075.6","gene_symbol":"POC1B-GALNT4","gene_name":"POC1B-GALNT4 readthrough [Source:HGNC Symbol;Acc:HGNC:42957]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528030","summary":"This locus represents naturally occurring transcripts that splice the 5' exons of the POC1B (POC1 centriolar protein homolog B) gene on chromosome 12 to the GALNT4 (UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 4) gene, which is located within a POC1B intron. Alternative splicing results in two transcript variants, one of which encodes a fusion isoform that shares sequence identity with the products of each individual gene. [provided by RefSeq, Dec 2010]","start":89519408,"end":89526262,"strand":-1,"description":"POC1B-GALNT4 readthrough [Source:HGNC Symbol;Acc:HGNC:42957]"}, {"versioned_ensembl_gene_id":"ENSG00000261384.1","gene_symbol":"AC023300.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74303005,"end":74304343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203706.8","gene_symbol":"SERTAD4-AS1","gene_name":"SERTAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32019]","synonyms":"C1orf133","biotype":"antisense_RNA","ncbi_id":"574036","summary":null,"start":210231456,"end":210234047,"strand":-1,"description":"SERTAD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32019]"}, {"versioned_ensembl_gene_id":"ENSG00000235827.2","gene_symbol":"TUBB8P9","gene_name":"tubulin beta 8 class VIII pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42347]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"255208","summary":null,"start":227506182,"end":227508292,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42347]"}, {"versioned_ensembl_gene_id":"ENSG00000234058.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30056599,"end":30060223,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000137868.18","gene_symbol":"STRA6","gene_name":"stimulated by retinoic acid 6 [Source:HGNC Symbol;Acc:HGNC:30650]","synonyms":"FLJ12541","biotype":"protein_coding","ncbi_id":"64220","summary":"The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":74179466,"end":74212267,"strand":-1,"description":"stimulated by retinoic acid 6 [Source:HGNC Symbol;Acc:HGNC:30650]"}, {"versioned_ensembl_gene_id":"ENSG00000263312.1","gene_symbol":"LINC01975","gene_name":"long intergenic non-protein coding RNA 1975 [Source:HGNC Symbol;Acc:HGNC:52802]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371496","summary":null,"start":3977103,"end":3981899,"strand":1,"description":"long intergenic non-protein coding RNA 1975 [Source:HGNC Symbol;Acc:HGNC:52802]"}, {"versioned_ensembl_gene_id":"ENSG00000279939.1","gene_symbol":"AC025034.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89544203,"end":89544488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248105.1","gene_symbol":"AC008885.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82824884,"end":82825184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231287.2","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"bQB90C11.3,HCG4P6,HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29920067,"end":29921057,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000280021.1","gene_symbol":"OR51F1","gene_name":"olfactory receptor family 51 subfamily F member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15196]","synonyms":"OR51F1P","biotype":"polymorphic_pseudogene","ncbi_id":"256892","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":4768979,"end":4769938,"strand":-1,"description":"olfactory receptor family 51 subfamily F member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15196]"}, {"versioned_ensembl_gene_id":"ENSG00000225003.1","gene_symbol":"OR51A5P","gene_name":"olfactory receptor family 51 subfamily A member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79525","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4972943,"end":4973884,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14801]"}, {"versioned_ensembl_gene_id":"ENSG00000176922.4","gene_symbol":"OR51S1","gene_name":"olfactory receptor family 51 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15204]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4847489,"end":4849238,"strand":-1,"description":"olfactory receptor family 51 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15204]"}, {"versioned_ensembl_gene_id":"ENSG00000227843.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"DDX6-Lp,bA150A6.3,DDX6P","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29330530,"end":29331965,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000144043.11","gene_symbol":"TEX261","gene_name":"testis expressed 261 [Source:HGNC Symbol;Acc:HGNC:30712]","synonyms":"TEG-261,MGC32043","biotype":"protein_coding","ncbi_id":"113419","summary":null,"start":70985938,"end":70994945,"strand":-1,"description":"testis expressed 261 [Source:HGNC Symbol;Acc:HGNC:30712]"}, {"versioned_ensembl_gene_id":"ENSG00000234896.1","gene_symbol":"OR7E62P","gene_name":"olfactory receptor family 7 subfamily E member 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:8438]","synonyms":"OR7E62,OR2-53,OR7E82P,OR7E64P,OR7E64,OR7E63P,OR7E63","biotype":"unprocessed_pseudogene","ncbi_id":"26479","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71055527,"end":71056003,"strand":1,"description":"olfactory receptor family 7 subfamily E member 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:8438]"}, {"versioned_ensembl_gene_id":"ENSG00000236469.1","gene_symbol":"AC007881.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71002531,"end":71064743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228375.1","gene_symbol":"RPS20P25","gene_name":"ribosomal protein S20 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271235","summary":null,"start":81410279,"end":81410630,"strand":1,"description":"ribosomal protein S20 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35866]"}, {"versioned_ensembl_gene_id":"ENSG00000179967.11","gene_symbol":"PPP1R14BP3","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16330]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507617","summary":null,"start":139114930,"end":139115374,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16330]"}, {"versioned_ensembl_gene_id":"ENSG00000151014.5","gene_symbol":"NOCT","gene_name":"nocturnin [Source:HGNC Symbol;Acc:HGNC:14254]","synonyms":"NOC,CCRN4L,CCR4L,Ccr4c","biotype":"protein_coding","ncbi_id":"25819","summary":"The protein encoded by this gene is highly similar to Nocturnin, a gene identified as a circadian clock regulated gene in Xenopus laevis. This protein and Nocturnin protein share similarity with the C-terminal domain of a yeast transcription factor, carbon catabolite repression 4 (CCR4). The mRNA abundance of a similar gene in mouse has been shown to exhibit circadian rhythmicity, which suggests a role for this protein in clock function or as a circadian clock effector. [provided by RefSeq, Jul 2008]","start":139015789,"end":139045939,"strand":1,"description":"nocturnin [Source:HGNC Symbol;Acc:HGNC:14254]"}, {"versioned_ensembl_gene_id":"ENSG00000279204.1","gene_symbol":"AC134043.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":159106380,"end":159108617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235438.7","gene_symbol":"ESRRAP2","gene_name":"estrogen-related receptor alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24647]","synonyms":"ESTRRA","biotype":"transcribed_processed_pseudogene","ncbi_id":"144832","summary":null,"start":21260015,"end":21295003,"strand":1,"description":"estrogen-related receptor alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24647]"}, {"versioned_ensembl_gene_id":"ENSG00000228729.1","gene_symbol":"AL627308.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227234269,"end":227235355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204889.10","gene_symbol":"KRT40","gene_name":"keratin 40 [Source:HGNC Symbol;Acc:HGNC:26707]","synonyms":"FLJ36600,KA36","biotype":"protein_coding","ncbi_id":"125115","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40977716,"end":40987135,"strand":-1,"description":"keratin 40 [Source:HGNC Symbol;Acc:HGNC:26707]"}, {"versioned_ensembl_gene_id":"ENSG00000123064.12","gene_symbol":"DDX54","gene_name":"DEAD-box helicase 54 [Source:HGNC Symbol;Acc:HGNC:20084]","synonyms":"MGC2835,DP97,APR-5","biotype":"protein_coding","ncbi_id":"79039","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The nucleolar protein encoded by this gene interacts in a hormone-dependent manner with nuclear receptors, and represses their transcriptional activity. Alternative splice variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":113157174,"end":113185479,"strand":-1,"description":"DEAD-box helicase 54 [Source:HGNC Symbol;Acc:HGNC:20084]"}, {"versioned_ensembl_gene_id":"ENSG00000249885.1","gene_symbol":"ARHGEF38-IT1","gene_name":"ARHGEF38 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41483]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874374","summary":null,"start":105561591,"end":105570238,"strand":1,"description":"ARHGEF38 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41483]"}, {"versioned_ensembl_gene_id":"ENSG00000258871.1","gene_symbol":"AC004828.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72552580,"end":72595125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278907.1","gene_symbol":"AC005609.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140849105,"end":140849696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231411.1","gene_symbol":"DUX4L31","gene_name":"double homeobox 4 like 31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51770]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100887073","summary":null,"start":10171590,"end":10172725,"strand":-1,"description":"double homeobox 4 like 31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51770]"}, {"versioned_ensembl_gene_id":"ENSG00000236559.1","gene_symbol":"AL117381.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31686216,"end":31716825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281376.1","gene_symbol":"ABALON","gene_name":"apoptotic BCL2L1-antisense long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49667]","synonyms":"INXS","biotype":"antisense_RNA","ncbi_id":"103021294","summary":null,"start":31721507,"end":31723409,"strand":1,"description":"apoptotic BCL2L1-antisense long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49667]"}, {"versioned_ensembl_gene_id":"ENSG00000196810.4","gene_symbol":"CTBP1-AS2","gene_name":"CTBP1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:28307]","synonyms":"MGC21675,CTBP1-AS1,C4orf42","biotype":"antisense_RNA","ncbi_id":"92070","summary":null,"start":1249300,"end":1288291,"strand":1,"description":"CTBP1 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:28307]"}, {"versioned_ensembl_gene_id":"ENSG00000225933.1","gene_symbol":"AC133965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87654890,"end":87655243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175110.11","gene_symbol":"MRPS22","gene_name":"mitochondrial ribosomal protein S22 [Source:HGNC Symbol;Acc:HGNC:14508]","synonyms":"GK002,MRP-S22,GIBT,C3orf5","biotype":"protein_coding","ncbi_id":"56945","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that does not seem to have a counterpart in prokaryotic and fungal-mitochondrial ribosomes. This gene lies telomeric of and is transcribed in the opposite direction from the forkhead box L2 gene. A pseudogene corresponding to this gene is found on chromosome Xq. [provided by RefSeq, Jul 2008]","start":139005806,"end":139357223,"strand":1,"description":"mitochondrial ribosomal protein S22 [Source:HGNC Symbol;Acc:HGNC:14508]"}, {"versioned_ensembl_gene_id":"ENSG00000032219.18","gene_symbol":"ARID4A","gene_name":"AT-rich interaction domain 4A [Source:HGNC Symbol;Acc:HGNC:9885]","synonyms":"RBP-1,RBBP1,RBP1","biotype":"protein_coding","ncbi_id":"5926","summary":"The protein encoded by this gene is a ubiquitously expressed nuclear protein. It binds directly, with several other proteins, to retinoblastoma protein (pRB) which regulates cell proliferation. pRB represses transcription by recruiting the encoded protein. This protein, in turn, serves as a bridging molecule to recruit HDACs and, in addition, provides a second HDAC-independent repression function. The encoded protein possesses transcriptional repression activity. Multiple alternatively spliced transcripts have been observed for this gene, although not all transcript variants have been fully described. [provided by RefSeq, Jul 2008]","start":58298385,"end":58373887,"strand":1,"description":"AT-rich interaction domain 4A [Source:HGNC Symbol;Acc:HGNC:9885]"}, {"versioned_ensembl_gene_id":"ENSG00000255445.1","gene_symbol":"AP003072.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93152075,"end":93152750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268764.1","gene_symbol":"AC011465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38108500,"end":38109533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237916.1","gene_symbol":"AC011753.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109552536,"end":109552846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233713.2","gene_symbol":"AL161447.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86132622,"end":86132851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259496.2","gene_symbol":"AC021818.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69803316,"end":69804046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171987.1","gene_symbol":"C11orf40","gene_name":"chromosome 11 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:23986]","synonyms":"NOV1","biotype":"protein_coding","ncbi_id":"143501","summary":null,"start":4571423,"end":4577820,"strand":-1,"description":"chromosome 11 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:23986]"}, {"versioned_ensembl_gene_id":"ENSG00000223478.1","gene_symbol":"AL441992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128724445,"end":128733194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197790.1","gene_symbol":"OR52M1","gene_name":"olfactory receptor family 52 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:15225]","synonyms":"OR52M1P","biotype":"protein_coding","ncbi_id":"119772","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4545191,"end":4546144,"strand":1,"description":"olfactory receptor family 52 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:15225]"}, {"versioned_ensembl_gene_id":"ENSG00000251278.1","gene_symbol":"AC006499.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10292195,"end":10292708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233924.1","gene_symbol":"RPSAP13","gene_name":"ribosomal protein SA pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6505]","synonyms":"LAMR1P13,LAMRP3,LAMRL3","biotype":"processed_pseudogene","ncbi_id":"3923","summary":null,"start":55004813,"end":55005687,"strand":-1,"description":"ribosomal protein SA pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:6505]"}, {"versioned_ensembl_gene_id":"ENSG00000197989.13","gene_symbol":"SNHG12","gene_name":"small nucleolar RNA host gene 12 [Source:HGNC Symbol;Acc:HGNC:30062]","synonyms":"PNAS-123,LINC00100,C1orf79,ASLNC04080","biotype":"antisense_RNA","ncbi_id":"85028","summary":"This gene produces a long RNA that is overexpressed in tumor cells. This RNA may promote tumorigenesis by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017]","start":28578538,"end":28582983,"strand":-1,"description":"small nucleolar RNA host gene 12 [Source:HGNC Symbol;Acc:HGNC:30062]"}, {"versioned_ensembl_gene_id":"ENSG00000254596.1","gene_symbol":"AP002748.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66454234,"end":66454581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103569.9","gene_symbol":"AQP9","gene_name":"aquaporin 9 [Source:HGNC Symbol;Acc:HGNC:643]","synonyms":"SSC1,HsT17287","biotype":"protein_coding","ncbi_id":"366","summary":"The aquaporins are a family of water-selective membrane channels. This gene encodes a member of a subset of aquaporins called the aquaglyceroporins. This protein allows passage of a broad range of noncharged solutes and also stimulates urea transport and osmotic water permeability. This protein may also facilitate the uptake of glycerol in hepatic tissue . The encoded protein may also play a role in specialized leukocyte functions such as immunological response and bactericidal activity. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":58138169,"end":58185911,"strand":1,"description":"aquaporin 9 [Source:HGNC Symbol;Acc:HGNC:643]"}, {"versioned_ensembl_gene_id":"ENSG00000226860.1","gene_symbol":"AC109638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82609652,"end":82609977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250393.1","gene_symbol":"AC093664.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10143367,"end":10143655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185347.17","gene_symbol":"C14orf80","gene_name":"chromosome 14 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:20127]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283643","summary":null,"start":105489855,"end":105499575,"strand":1,"description":"chromosome 14 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:20127]"}, {"versioned_ensembl_gene_id":"ENSG00000233960.1","gene_symbol":"AC079763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52165235,"end":52192913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229478.1","gene_symbol":"ROBO2P1","gene_name":"roundabout guidance receptor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44386]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480790","summary":null,"start":51600286,"end":51600573,"strand":-1,"description":"roundabout guidance receptor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44386]"}, {"versioned_ensembl_gene_id":"ENSG00000251495.1","gene_symbol":"PPIAP11","gene_name":"peptidylprolyl isomerase A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:9263]","synonyms":"PPIP1","biotype":"processed_pseudogene","ncbi_id":"5483","summary":null,"start":82009602,"end":82010094,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:9263]"}, {"versioned_ensembl_gene_id":"ENSG00000277701.4","gene_symbol":"AC159540.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97281904,"end":97291780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267250.1","gene_symbol":"AC011591.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68793549,"end":68797822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231781.1","gene_symbol":"AC079896.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81983272,"end":82005700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254874.1","gene_symbol":"AP003171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92965797,"end":92966603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214188.9","gene_symbol":"ST7-OT4","gene_name":"ST7 overlapping transcript 4 [Source:HGNC Symbol;Acc:HGNC:18835]","synonyms":"ST7OT4,NCRNA00042","biotype":"sense_intronic","ncbi_id":"338069","summary":null,"start":116953899,"end":117098806,"strand":1,"description":"ST7 overlapping transcript 4 [Source:HGNC Symbol;Acc:HGNC:18835]"}, {"versioned_ensembl_gene_id":"ENSG00000186395.7","gene_symbol":"KRT10","gene_name":"keratin 10 [Source:HGNC Symbol;Acc:HGNC:6413]","synonyms":"KPP,K10,CK10","biotype":"protein_coding","ncbi_id":"3858","summary":"This gene encodes a member of the type I (acidic) cytokeratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. Mutations in this gene are associated with epidermolytic hyperkeratosis. This gene is located within a cluster of keratin family members on chromosome 17q21. [provided by RefSeq, Jul 2008]","start":40818117,"end":40822595,"strand":-1,"description":"keratin 10 [Source:HGNC Symbol;Acc:HGNC:6413]"}, {"versioned_ensembl_gene_id":"ENSG00000227199.1","gene_symbol":"ST7-AS1","gene_name":"ST7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16000]","synonyms":"ST7OT1,ST7AS1","biotype":"antisense_RNA","ncbi_id":"93653","summary":null,"start":116952446,"end":116954334,"strand":-1,"description":"ST7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16000]"}, {"versioned_ensembl_gene_id":"ENSG00000268361.1","gene_symbol":"L34079.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43554692,"end":43593036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000051382.8","gene_symbol":"PIK3CB","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:8976]","synonyms":"PIK3C1","biotype":"protein_coding","ncbi_id":"5291","summary":"This gene encodes an isoform of the catalytic subunit of phosphoinositide 3-kinase (PI3K). These kinases are important in signaling pathways involving receptors on the outer membrane of eukaryotic cells and are named for their catalytic subunit. The encoded protein is the catalytic subunit for PI3Kbeta (PI3KB). PI3KB has been shown to be part of the activation pathway in neutrophils which have bound immune complexes at sites of injury or infection. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":138652699,"end":138834938,"strand":-1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:8976]"}, {"versioned_ensembl_gene_id":"ENSG00000278710.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850408,"end":54867186,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000225868.7","gene_symbol":"AC016582.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37823722,"end":37855215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267598.1","gene_symbol":"AC011446.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13153071,"end":13154193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230948.1","gene_symbol":"AP001331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108131100,"end":108132114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175800.5","gene_symbol":"OR52B3P","gene_name":"olfactory receptor family 52 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15208]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"387747","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4378282,"end":4379209,"strand":1,"description":"olfactory receptor family 52 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15208]"}, {"versioned_ensembl_gene_id":"ENSG00000283873.1","gene_symbol":"AC018793.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4287499,"end":4288083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167378.8","gene_symbol":"IRGQ","gene_name":"immunity related GTPase Q [Source:HGNC Symbol;Acc:HGNC:24868]","synonyms":"IRGQ1,FKSG27","biotype":"protein_coding","ncbi_id":"126298","summary":null,"start":43584369,"end":43596135,"strand":-1,"description":"immunity related GTPase Q [Source:HGNC Symbol;Acc:HGNC:24868]"}, {"versioned_ensembl_gene_id":"ENSG00000269177.1","gene_symbol":"L34079.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43553445,"end":43555494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243829.1","gene_symbol":"AC011495.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49719498,"end":49720081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251652.1","gene_symbol":"AC092535.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1113639,"end":1132977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255652.3","gene_symbol":"AC140847.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34191279,"end":34218853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000009790.14","gene_symbol":"TRAF3IP3","gene_name":"TRAF3 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:30766]","synonyms":"T3JAM","biotype":"protein_coding","ncbi_id":"80342","summary":"The gene encodes a protein that mediates cell growth by modulating the c-Jun N-terminal kinase signal transduction pathway. The encoded protein may also interact with a large multi-protein assembly containing the phosphatase 2A catalytic subunit. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":209756032,"end":209782320,"strand":1,"description":"TRAF3 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:30766]"}, {"versioned_ensembl_gene_id":"ENSG00000175535.6","gene_symbol":"PNLIP","gene_name":"pancreatic lipase [Source:HGNC Symbol;Acc:HGNC:9155]","synonyms":"PL","biotype":"protein_coding","ncbi_id":"5406","summary":"This gene encodes a member of the lipase family of proteins. The encoded enzyme is secreted by the pancreas and hydrolyzes triglycerides in the small intestine, and is essential for the efficient digestion of dietary fats. Inhibition of the encoded enzyme may prevent high-fat diet-induced obesity in mice and result in weight loss in human patients with obesity. Mutations in this gene cause congenital pancreatic lipase deficiency, a rare disorder characterized by steatorrhea. [provided by RefSeq, Jul 2016]","start":116545931,"end":116567855,"strand":1,"description":"pancreatic lipase [Source:HGNC Symbol;Acc:HGNC:9155]"}, {"versioned_ensembl_gene_id":"ENSG00000254551.1","gene_symbol":"AP000873.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83209431,"end":83213379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237494.1","gene_symbol":"AL360007.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142251847,"end":142259632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105258.8","gene_symbol":"POLR2I","gene_name":"RNA polymerase II subunit I [Source:HGNC Symbol;Acc:HGNC:9196]","synonyms":"RPB9,hRPB14.5","biotype":"protein_coding","ncbi_id":"5438","summary":"This gene encodes a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This subunit, in combination with two other polymerase subunits, forms the DNA binding domain of the polymerase, a groove in which the DNA template is transcribed into RNA. The product of this gene has two zinc finger motifs with conserved cysteines and the subunit does possess zinc binding activity. [provided by RefSeq, Jul 2008]","start":36113710,"end":36115346,"strand":-1,"description":"RNA polymerase II subunit I [Source:HGNC Symbol;Acc:HGNC:9196]"}, {"versioned_ensembl_gene_id":"ENSG00000178053.17","gene_symbol":"MLF1","gene_name":"myeloid leukemia factor 1 [Source:HGNC Symbol;Acc:HGNC:7125]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4291","summary":"This gene encodes an oncoprotein which is thought to play a role in the phenotypic determination of hemopoetic cells. Translocations between this gene and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]","start":158571163,"end":158607252,"strand":1,"description":"myeloid leukemia factor 1 [Source:HGNC Symbol;Acc:HGNC:7125]"}, {"versioned_ensembl_gene_id":"ENSG00000250259.1","gene_symbol":"AC019103.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1027678,"end":1028972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253523.1","gene_symbol":"AC104350.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58031334,"end":58032682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131747.14","gene_symbol":"TOP2A","gene_name":"topoisomerase (DNA) II alpha [Source:HGNC Symbol;Acc:HGNC:11989]","synonyms":"TOP2","biotype":"protein_coding","ncbi_id":"7153","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional stress that occurs during DNA transcription and replication. It catalyzes the transient breaking and rejoining of two strands of duplex DNA which allows the strands to pass through one another, thus altering the topology of DNA. Two forms of this enzyme exist as likely products of a gene duplication event. The gene encoding this form, alpha, is localized to chromosome 17 and the beta gene is localized to chromosome 3. The gene encoding this enzyme functions as the target for several anticancer agents and a variety of mutations in this gene have been associated with the development of drug resistance. Reduced activity of this enzyme may also play a role in ataxia-telangiectasia. [provided by RefSeq, Jul 2010]","start":40388516,"end":40417950,"strand":-1,"description":"topoisomerase (DNA) II alpha [Source:HGNC Symbol;Acc:HGNC:11989]"}, {"versioned_ensembl_gene_id":"ENSG00000131469.12","gene_symbol":"RPL27","gene_name":"ribosomal protein L27 [Source:HGNC Symbol;Acc:HGNC:10328]","synonyms":"L27","biotype":"protein_coding","ncbi_id":"6155","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L27e family of ribosomal proteins and a component of the 60S subunit. A splice site mutation in this gene has been identified in a Diamond-Blackfan anemia (DBA) patient. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Mar 2017]","start":42998273,"end":43002959,"strand":1,"description":"ribosomal protein L27 [Source:HGNC Symbol;Acc:HGNC:10328]"}, {"versioned_ensembl_gene_id":"ENSG00000104936.17","gene_symbol":"DMPK","gene_name":"DM1 protein kinase [Source:HGNC Symbol;Acc:HGNC:2933]","synonyms":"MDPK,DMK,DM1PK,DM1,DM,MT-PK","biotype":"protein_coding","ncbi_id":"1760","summary":"The protein encoded by this gene is a serine-threonine kinase that is closely related to other kinases that interact with members of the Rho family of small GTPases. Substrates for this enzyme include myogenin, the beta-subunit of the L-type calcium channels, and phospholemman. The 3' untranslated region of this gene contains 5-38 copies of a CTG trinucleotide repeat. Expansion of this unstable motif to 50-5,000 copies causes myotonic dystrophy type I, which increases in severity with increasing repeat element copy number. Repeat expansion is associated with condensation of local chromatin structure that disrupts the expression of genes in this region. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2016]","start":45769717,"end":45782552,"strand":-1,"description":"DM1 protein kinase [Source:HGNC Symbol;Acc:HGNC:2933]"}, {"versioned_ensembl_gene_id":"ENSG00000265666.1","gene_symbol":"RARA-AS1","gene_name":"RARA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49577]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929693","summary":null,"start":40340867,"end":40343136,"strand":-1,"description":"RARA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49577]"}, {"versioned_ensembl_gene_id":"ENSG00000172301.10","gene_symbol":"COPRS","gene_name":"coordinator of PRMT5 and differentiation stimulator [Source:HGNC Symbol;Acc:HGNC:28848]","synonyms":"TTP1,HSA272196,COPR5,C17orf79","biotype":"protein_coding","ncbi_id":"55352","summary":null,"start":31851864,"end":31859337,"strand":-1,"description":"coordinator of PRMT5 and differentiation stimulator [Source:HGNC Symbol;Acc:HGNC:28848]"}, {"versioned_ensembl_gene_id":"ENSG00000279917.1","gene_symbol":"AC079331.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67611277,"end":67613822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282756.1","gene_symbol":"TRBV7-4","gene_name":"T-cell receptor beta variable 7-4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12238]","synonyms":"TRBV74,TCRBV7S4,TCRBV6S8A2T","biotype":"TR_V_gene","ncbi_id":"28594","summary":null,"start":142476873,"end":142477334,"strand":1,"description":"T-cell receptor beta variable 7-4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12238]"}, {"versioned_ensembl_gene_id":"ENSG00000163346.16","gene_symbol":"PBXIP1","gene_name":"PBX homeobox interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21199]","synonyms":"HPIP","biotype":"protein_coding","ncbi_id":"57326","summary":"The protein encoded by this gene interacts with the PBX1 homeodomain protein, inhibiting its transcriptional activation potential by preventing its binding to DNA. The encoded protein, which is primarily cytosolic but can shuttle to the nucleus, also can interact with estrogen receptors alpha and beta and promote the proliferation of breast cancer, brain tumors, and lung cancer. Several transcript variants encoding different isoforms have been found for this gene. More variants exist, but their full-length natures have yet to be determined. [provided by RefSeq, Dec 2015]","start":154944076,"end":154956123,"strand":-1,"description":"PBX homeobox interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21199]"}, {"versioned_ensembl_gene_id":"ENSG00000264754.1","gene_symbol":"AC110921.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":67524481,"end":67525422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157303.10","gene_symbol":"SUSD3","gene_name":"sushi domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28391]","synonyms":"MGC26847","biotype":"protein_coding","ncbi_id":"203328","summary":null,"start":93058688,"end":93085138,"strand":1,"description":"sushi domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28391]"}, {"versioned_ensembl_gene_id":"ENSG00000248483.6","gene_symbol":"POU5F2","gene_name":"POU domain class 5, transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:26367]","synonyms":"SPRM-1,FLJ25680","biotype":"protein_coding","ncbi_id":"134187","summary":null,"start":93733220,"end":93741637,"strand":-1,"description":"POU domain class 5, transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:26367]"}, {"versioned_ensembl_gene_id":"ENSG00000259895.1","gene_symbol":"AC106820.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2464950,"end":2468213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244556.1","gene_symbol":"ODCP","gene_name":"ornithine decarboxylase pseudogene [Source:HGNC Symbol;Acc:HGNC:8110]","synonyms":"ODC2","biotype":"processed_pseudogene","ncbi_id":"4954","summary":null,"start":129028889,"end":129030527,"strand":1,"description":"ornithine decarboxylase pseudogene [Source:HGNC Symbol;Acc:HGNC:8110]"}, {"versioned_ensembl_gene_id":"ENSG00000215117.5","gene_symbol":"LINC00588","gene_name":"long intergenic non-protein coding RNA 588 [Source:HGNC Symbol;Acc:HGNC:24494]","synonyms":"DKFZP434F122,C8orf71","biotype":"lincRNA","ncbi_id":"26138","summary":null,"start":57279543,"end":57284731,"strand":1,"description":"long intergenic non-protein coding RNA 588 [Source:HGNC Symbol;Acc:HGNC:24494]"}, {"versioned_ensembl_gene_id":"ENSG00000253614.1","gene_symbol":"AC025674.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57261226,"end":57266613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131759.17","gene_symbol":"RARA","gene_name":"retinoic acid receptor alpha [Source:HGNC Symbol;Acc:HGNC:9864]","synonyms":"NR1B1,RAR","biotype":"protein_coding","ncbi_id":"5914","summary":"This gene represents a nuclear retinoic acid receptor. The encoded protein, retinoic acid receptor alpha, regulates transcription in a ligand-dependent manner. This gene has been implicated in regulation of development, differentiation, apoptosis, granulopoeisis, and transcription of clock genes. Translocations between this locus and several other loci have been associated with acute promyelocytic leukemia. Alternatively spliced transcript variants have been found for this locus.[provided by RefSeq, Sep 2010]","start":40309192,"end":40357643,"strand":1,"description":"retinoic acid receptor alpha [Source:HGNC Symbol;Acc:HGNC:9864]"}, {"versioned_ensembl_gene_id":"ENSG00000183444.10","gene_symbol":"OR7E38P","gene_name":"olfactory receptor family 7 subfamily E member 38 pseudogene [Source:HGNC Symbol;Acc:HGNC:8411]","synonyms":"OST127,OR7E76","biotype":"unprocessed_pseudogene","ncbi_id":"389537","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":97966090,"end":97967074,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 38 pseudogene [Source:HGNC Symbol;Acc:HGNC:8411]"}, {"versioned_ensembl_gene_id":"ENSG00000177383.4","gene_symbol":"MAGEF1","gene_name":"MAGE family member F1 [Source:HGNC Symbol;Acc:HGNC:29639]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64110","summary":"This intronless gene encodes a member of the MAGE superfamily. It is ubiquitously expressed in normal tissues and in tumor cells. This gene includes a microsatellite repeat in the coding region. [provided by RefSeq, Jul 2008]","start":184710367,"end":184712002,"strand":-1,"description":"MAGE family member F1 [Source:HGNC Symbol;Acc:HGNC:29639]"}, {"versioned_ensembl_gene_id":"ENSG00000221819.5","gene_symbol":"GAS8-AS1","gene_name":"GAS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1197]","synonyms":"C16orf3","biotype":"antisense_RNA","ncbi_id":"750","summary":"This gene encodes a long non-coding RNA (lncRNA) that may function as a tumor suppressor. Mutations in this gene have been identified in human papillary thyroid carcinoma (PTC) patients that abrogate the ability of encoded lncRNA to inhibit cancer cell growth. [provided by RefSeq, May 2017]","start":90028908,"end":90029367,"strand":-1,"description":"GAS8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1197]"}, {"versioned_ensembl_gene_id":"ENSG00000109220.10","gene_symbol":"CHIC2","gene_name":"cysteine rich hydrophobic domain 2 [Source:HGNC Symbol;Acc:HGNC:1935]","synonyms":"BTL","biotype":"protein_coding","ncbi_id":"26511","summary":"This gene encodes a member of the CHIC family of proteins. The encoded protein contains a cysteine-rich hydrophobic (CHIC) motif, and is localized to vesicular structures and the plasma membrane. This gene is associated with some cases of acute myeloid leukemia. [provided by RefSeq, Jul 2008]","start":54009789,"end":54064690,"strand":-1,"description":"cysteine rich hydrophobic domain 2 [Source:HGNC Symbol;Acc:HGNC:1935]"}, {"versioned_ensembl_gene_id":"ENSG00000144199.11","gene_symbol":"FAHD2B","gene_name":"fumarylacetoacetate hydrolase domain containing 2B [Source:HGNC Symbol;Acc:HGNC:25318]","synonyms":"DKFZp434N062","biotype":"protein_coding","ncbi_id":"151313","summary":null,"start":97083583,"end":97094882,"strand":-1,"description":"fumarylacetoacetate hydrolase domain containing 2B [Source:HGNC Symbol;Acc:HGNC:25318]"}, {"versioned_ensembl_gene_id":"ENSG00000167766.18","gene_symbol":"ZNF83","gene_name":"zinc finger protein 83 [Source:HGNC Symbol;Acc:HGNC:13158]","synonyms":"ZNF816B,HPF1,FLJ11015","biotype":"protein_coding","ncbi_id":"55769","summary":null,"start":52594060,"end":52690496,"strand":-1,"description":"zinc finger protein 83 [Source:HGNC Symbol;Acc:HGNC:13158]"}, {"versioned_ensembl_gene_id":"ENSG00000148136.5","gene_symbol":"OR13C4","gene_name":"olfactory receptor family 13 subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:14722]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138804","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104526253,"end":104527209,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:14722]"}, {"versioned_ensembl_gene_id":"ENSG00000129682.15","gene_symbol":"FGF13","gene_name":"fibroblast growth factor 13 [Source:HGNC Symbol;Acc:HGNC:3670]","synonyms":"FHF2,FGF2","biotype":"protein_coding","ncbi_id":"2258","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]","start":138614731,"end":139222777,"strand":-1,"description":"fibroblast growth factor 13 [Source:HGNC Symbol;Acc:HGNC:3670]"}, {"versioned_ensembl_gene_id":"ENSG00000205838.13","gene_symbol":"TTC23L","gene_name":"tetratricopeptide repeat domain 23 like [Source:HGNC Symbol;Acc:HGNC:26355]","synonyms":"FLJ25439","biotype":"protein_coding","ncbi_id":"153657","summary":null,"start":34838833,"end":34899456,"strand":1,"description":"tetratricopeptide repeat domain 23 like [Source:HGNC Symbol;Acc:HGNC:26355]"}, {"versioned_ensembl_gene_id":"ENSG00000104064.16","gene_symbol":"GABPB1","gene_name":"GA binding protein transcription factor beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:4074]","synonyms":"GABPB2,GABPB,E4TF1-47","biotype":"protein_coding","ncbi_id":"2553","summary":"This gene encodes the GA-binding protein transcription factor, beta subunit. This protein forms a tetrameric complex with the alpha subunit, and stimulates transcription of target genes. The encoded protein may be involved in activation of cytochrome oxidase expression and nuclear control of mitochondrial function. The crystal structure of a similar protein in mouse has been resolved as a ternary protein complex. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":50275392,"end":50355408,"strand":-1,"description":"GA binding protein transcription factor beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:4074]"}, {"versioned_ensembl_gene_id":"ENSG00000137760.14","gene_symbol":"ALKBH8","gene_name":"alkB homolog 8, tRNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:25189]","synonyms":"TRM9,MGC10235","biotype":"protein_coding","ncbi_id":"91801","summary":null,"start":107502726,"end":107565746,"strand":-1,"description":"alkB homolog 8, tRNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:25189]"}, {"versioned_ensembl_gene_id":"ENSG00000185513.14","gene_symbol":"L3MBTL1","gene_name":"L3MBTL1, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:15905]","synonyms":"ZC2HC3,L3MBTL,KIAA0681,DKFZp586P1522,dJ138B7.3","biotype":"protein_coding","ncbi_id":"26013","summary":"This gene represents a polycomb group gene. The encoded protein functions to regulate gene activity, likely via chromatin modification. The encoded protein may also be necessary for mitosis. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]","start":43507680,"end":43550950,"strand":1,"description":"L3MBTL1, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:15905]"}, {"versioned_ensembl_gene_id":"ENSG00000054179.11","gene_symbol":"ENTPD2","gene_name":"ectonucleoside triphosphate diphosphohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:3364]","synonyms":"NTPDase-2,CD39L1","biotype":"protein_coding","ncbi_id":"954","summary":"The protein encoded by this gene is the type 2 enzyme of the ecto-nucleoside triphosphate diphosphohydrolase family (E-NTPDase). E-NTPDases are a family of ecto-nucleosidases that hydrolyze 5'-triphosphates. This ecto-ATPase is an integral membrane protein. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":137048098,"end":137054045,"strand":-1,"description":"ectonucleoside triphosphate diphosphohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:3364]"}, {"versioned_ensembl_gene_id":"ENSG00000198718.12","gene_symbol":"TOGARAM1","gene_name":"TOG array regulator of axonemal microtubules 1 [Source:HGNC Symbol;Acc:HGNC:19959]","synonyms":"KIAA0423,FAM179B,Crescerin-1,crescerin","biotype":"protein_coding","ncbi_id":"23116","summary":null,"start":44962208,"end":45074431,"strand":1,"description":"TOG array regulator of axonemal microtubules 1 [Source:HGNC Symbol;Acc:HGNC:19959]"}, {"versioned_ensembl_gene_id":"ENSG00000082641.15","gene_symbol":"NFE2L1","gene_name":"nuclear factor, erythroid 2 like 1 [Source:HGNC Symbol;Acc:HGNC:7781]","synonyms":"TCF11,NRF1,LCR-F1,FLJ00380","biotype":"protein_coding","ncbi_id":"4779","summary":"This gene encodes a protein that is involved in globin gene expression in erythrocytes. Confusion has occurred in bibliographic databases due to the shared symbol of NRF1 for this gene, NFE2L1, and for \"nuclear respiratory factor 1\" which has an official symbol of NRF1. [provided by RefSeq, Jul 2008]","start":48048329,"end":48061487,"strand":1,"description":"nuclear factor, erythroid 2 like 1 [Source:HGNC Symbol;Acc:HGNC:7781]"}, {"versioned_ensembl_gene_id":"ENSG00000269506.2","gene_symbol":"AC110792.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54059597,"end":54061210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214174.8","gene_symbol":"AMZ2P1","gene_name":"archaelysin family metallopeptidase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26491]","synonyms":"FLJ32065","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"201283","summary":null,"start":64966550,"end":64975576,"strand":-1,"description":"archaelysin family metallopeptidase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26491]"}, {"versioned_ensembl_gene_id":"ENSG00000102575.10","gene_symbol":"ACP5","gene_name":"acid phosphatase 5, tartrate resistant [Source:HGNC Symbol;Acc:HGNC:124]","synonyms":"HPAP,TRAP","biotype":"protein_coding","ncbi_id":"54","summary":"This gene encodes an iron containing glycoprotein which catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate. It is the most basic of the acid phosphatases and is the only form not inhibited by L(+)-tartrate. [provided by RefSeq, Aug 2008]","start":11574660,"end":11579008,"strand":-1,"description":"acid phosphatase 5, tartrate resistant [Source:HGNC Symbol;Acc:HGNC:124]"}, {"versioned_ensembl_gene_id":"ENSG00000189013.14","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803535,"end":54814517,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000049130.14","gene_symbol":"KITLG","gene_name":"KIT ligand [Source:HGNC Symbol;Acc:HGNC:6343]","synonyms":"SF,SCF,MGF,KL-1,Kitl,FPH2","biotype":"protein_coding","ncbi_id":"4254","summary":"This gene encodes the ligand of the tyrosine-kinase receptor encoded by the KIT locus. This ligand is a pleiotropic factor that acts in utero in germ cell and neural cell development, and hematopoiesis, all believed to reflect a role in cell migration. In adults, it functions pleiotropically, while mostly noted for its continued requirement in hematopoiesis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":88492793,"end":88580851,"strand":-1,"description":"KIT ligand [Source:HGNC Symbol;Acc:HGNC:6343]"}, {"versioned_ensembl_gene_id":"ENSG00000256659.1","gene_symbol":"LINC02368","gene_name":"long intergenic non-protein coding RNA 2368 [Source:HGNC Symbol;Acc:HGNC:53291]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927694","summary":null,"start":128118217,"end":128121952,"strand":1,"description":"long intergenic non-protein coding RNA 2368 [Source:HGNC Symbol;Acc:HGNC:53291]"}, {"versioned_ensembl_gene_id":"ENSG00000271111.1","gene_symbol":"AL365503.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67456346,"end":67457250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263622.1","gene_symbol":"AC023394.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65917782,"end":65920942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277734.7","gene_symbol":"TRAC","gene_name":"T-cell receptor alpha constant [Source:HGNC Symbol;Acc:HGNC:12029]","synonyms":null,"biotype":"TR_C_gene","ncbi_id":"28755","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22547506,"end":22552154,"strand":1,"description":"T-cell receptor alpha constant [Source:HGNC Symbol;Acc:HGNC:12029]"}, {"versioned_ensembl_gene_id":"ENSG00000270052.1","gene_symbol":"BX546450.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151497726,"end":151498354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211882.1","gene_symbol":"TRAJ7","gene_name":"T-cell receptor alpha joining 7 [Source:HGNC Symbol;Acc:HGNC:12095]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28748","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22537622,"end":22537680,"strand":1,"description":"T-cell receptor alpha joining 7 [Source:HGNC Symbol;Acc:HGNC:12095]"}, {"versioned_ensembl_gene_id":"ENSG00000211881.1","gene_symbol":"TRAJ8","gene_name":"T-cell receptor alpha joining 8 [Source:HGNC Symbol;Acc:HGNC:12096]","synonyms":null,"biotype":"TR_J_pseudogene","ncbi_id":"28747","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22536145,"end":22536204,"strand":1,"description":"T-cell receptor alpha joining 8 [Source:HGNC Symbol;Acc:HGNC:12096]"}, {"versioned_ensembl_gene_id":"ENSG00000254710.1","gene_symbol":"AP001970.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123188802,"end":123228277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220842.6","gene_symbol":"RPL21P16","gene_name":"ribosomal protein L21 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:31396]","synonyms":"Em:AC073587.1","biotype":"processed_pseudogene","ncbi_id":"729402","summary":null,"start":120354701,"end":120355183,"strand":-1,"description":"ribosomal protein L21 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:31396]"}, {"versioned_ensembl_gene_id":"ENSG00000167395.10","gene_symbol":"ZNF646","gene_name":"zinc finger protein 646 [Source:HGNC Symbol;Acc:HGNC:29004]","synonyms":"KIAA0296","biotype":"protein_coding","ncbi_id":"9726","summary":null,"start":31074422,"end":31084196,"strand":1,"description":"zinc finger protein 646 [Source:HGNC Symbol;Acc:HGNC:29004]"}, {"versioned_ensembl_gene_id":"ENSG00000225916.1","gene_symbol":"AC007879.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207226949,"end":207228308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105516.10","gene_symbol":"DBP","gene_name":"D-box binding PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:2697]","synonyms":"DABP","biotype":"protein_coding","ncbi_id":"1628","summary":"The protein encoded by this gene is a member of the PAR bZIP transcription factor family and binds to specific sequences in the promoters of several genes, such as albumin, CYP2A4, and CYP2A5. The encoded protein can bind DNA as a homo- or heterodimer and is involved in the regulation of some circadian rhythm genes. [provided by RefSeq, Jul 2014]","start":48630030,"end":48637438,"strand":-1,"description":"D-box binding PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:2697]"}, {"versioned_ensembl_gene_id":"ENSG00000221836.3","gene_symbol":"OR2A5","gene_name":"olfactory receptor family 2 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:8232]","synonyms":"OR2A8,OR2A26,OR7-141,OR7-138","biotype":"protein_coding","ncbi_id":"393046","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144048948,"end":144058845,"strand":1,"description":"olfactory receptor family 2 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:8232]"}, {"versioned_ensembl_gene_id":"ENSG00000140743.7","gene_symbol":"CDR2","gene_name":"cerebellar degeneration related protein 2 [Source:HGNC Symbol;Acc:HGNC:1799]","synonyms":"Yo,CDR62","biotype":"protein_coding","ncbi_id":"1039","summary":null,"start":22345936,"end":22437165,"strand":-1,"description":"cerebellar degeneration related protein 2 [Source:HGNC Symbol;Acc:HGNC:1799]"}, {"versioned_ensembl_gene_id":"ENSG00000156925.11","gene_symbol":"ZIC3","gene_name":"Zic family member 3 [Source:HGNC Symbol;Acc:HGNC:12874]","synonyms":"ZNF203,HTX1,HTX","biotype":"protein_coding","ncbi_id":"7547","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This nuclear protein probably functions as a transcription factor in early stages of left-right body axis formation. Mutations in this gene cause X-linked visceral heterotaxy, which includes congenital heart disease and left-right axis defects in organs. [provided by RefSeq, Jul 2008]","start":137566142,"end":137577691,"strand":1,"description":"Zic family member 3 [Source:HGNC Symbol;Acc:HGNC:12874]"}, {"versioned_ensembl_gene_id":"ENSG00000227508.6","gene_symbol":"LINC01624","gene_name":"long intergenic non-protein coding RNA 1624 [Source:HGNC Symbol;Acc:HGNC:52051]","synonyms":"TCONS_00011425","biotype":"lincRNA","ncbi_id":"401289","summary":null,"start":170272474,"end":170279887,"strand":1,"description":"long intergenic non-protein coding RNA 1624 [Source:HGNC Symbol;Acc:HGNC:52051]"}, {"versioned_ensembl_gene_id":"ENSG00000174456.13","gene_symbol":"C12orf76","gene_name":"chromosome 12 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:33790]","synonyms":"FLJ40142","biotype":"protein_coding","ncbi_id":"400073","summary":null,"start":110027028,"end":110073686,"strand":-1,"description":"chromosome 12 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:33790]"}, {"versioned_ensembl_gene_id":"ENSG00000146386.7","gene_symbol":"ABRACL","gene_name":"ABRA C-terminal like [Source:HGNC Symbol;Acc:HGNC:21230]","synonyms":"PRO2013,HSPC280,Costars,C6orf115","biotype":"protein_coding","ncbi_id":"58527","summary":null,"start":139028682,"end":139043302,"strand":1,"description":"ABRA C-terminal like [Source:HGNC Symbol;Acc:HGNC:21230]"}, {"versioned_ensembl_gene_id":"ENSG00000253160.1","gene_symbol":"AC105185.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39309909,"end":39310443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255563.1","gene_symbol":"AC021006.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41660030,"end":41660221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211866.1","gene_symbol":"TRAJ23","gene_name":"T-cell receptor alpha joining 23 [Source:HGNC Symbol;Acc:HGNC:12052]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28732","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22520416,"end":22520478,"strand":1,"description":"T-cell receptor alpha joining 23 [Source:HGNC Symbol;Acc:HGNC:12052]"}, {"versioned_ensembl_gene_id":"ENSG00000225807.1","gene_symbol":"AC069281.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100509717,"end":100519926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230960.1","gene_symbol":"AL109910.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170254334,"end":170262569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218716.1","gene_symbol":"RPL12P23","gene_name":"ribosomal protein L12 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36408]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270925","summary":null,"start":170199769,"end":170200258,"strand":1,"description":"ribosomal protein L12 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36408]"}, {"versioned_ensembl_gene_id":"ENSG00000158480.10","gene_symbol":"SPATA2","gene_name":"spermatogenesis associated 2 [Source:HGNC Symbol;Acc:HGNC:14681]","synonyms":"tamo,PPP1R145,PD1,KIAA0757","biotype":"protein_coding","ncbi_id":"9825","summary":null,"start":49903391,"end":49915508,"strand":-1,"description":"spermatogenesis associated 2 [Source:HGNC Symbol;Acc:HGNC:14681]"}, {"versioned_ensembl_gene_id":"ENSG00000254418.1","gene_symbol":"SPON1-AS1","gene_name":"SPON1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53117]","synonyms":"RP11-21,L19.1","biotype":"antisense_RNA","ncbi_id":"109729138","summary":null,"start":14262846,"end":14273691,"strand":-1,"description":"SPON1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53117]"}, {"versioned_ensembl_gene_id":"ENSG00000261616.1","gene_symbol":"AC036108.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99139317,"end":99145370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259921.1","gene_symbol":"AC022819.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":99157231,"end":99161140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267219.1","gene_symbol":"AC010504.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34348356,"end":34359412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280639.1","gene_symbol":"LINC02204","gene_name":"long intergenic non-protein coding RNA 2204 [Source:HGNC Symbol;Acc:HGNC:53070]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929151","summary":null,"start":70570958,"end":70586606,"strand":-1,"description":"long intergenic non-protein coding RNA 2204 [Source:HGNC Symbol;Acc:HGNC:53070]"}, {"versioned_ensembl_gene_id":"ENSG00000214748.2","gene_symbol":"AL355309.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137324972,"end":137325049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163577.7","gene_symbol":"EIF5A2","gene_name":"eukaryotic translation initiation factor 5A2 [Source:HGNC Symbol;Acc:HGNC:3301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56648","summary":null,"start":170888415,"end":170908693,"strand":-1,"description":"eukaryotic translation initiation factor 5A2 [Source:HGNC Symbol;Acc:HGNC:3301]"}, {"versioned_ensembl_gene_id":"ENSG00000261815.1","gene_symbol":"AC044798.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49170552,"end":49171786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250304.2","gene_symbol":"ZBED1P1","gene_name":"zinc finger BED-type containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645145","summary":null,"start":110291644,"end":110293573,"strand":1,"description":"zinc finger BED-type containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44004]"}, {"versioned_ensembl_gene_id":"ENSG00000225215.1","gene_symbol":"SMARCE1P1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39731]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271884","summary":null,"start":107403404,"end":107404589,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39731]"}, {"versioned_ensembl_gene_id":"ENSG00000120896.13","gene_symbol":"SORBS3","gene_name":"sorbin and SH3 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30907]","synonyms":"vinexin,SH3D4,SCAM-1","biotype":"protein_coding","ncbi_id":"10174","summary":"This gene encodes an SH3 domain-containing adaptor protein. The presence of SH3 domains play a role in this protein's ability to bind other cytoplasmic molecules and contribute to cystoskeletal organization, cell adhesion and migration, signaling, and gene expression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":22544986,"end":22575788,"strand":1,"description":"sorbin and SH3 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30907]"}, {"versioned_ensembl_gene_id":"ENSG00000107165.12","gene_symbol":"TYRP1","gene_name":"tyrosinase related protein 1 [Source:HGNC Symbol;Acc:HGNC:12450]","synonyms":"TYRP,TRP,OCA3,GP75,CATB,CAS2,b-PROTEIN","biotype":"protein_coding","ncbi_id":"7306","summary":"This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq, Mar 2009]","start":12685439,"end":12710290,"strand":1,"description":"tyrosinase related protein 1 [Source:HGNC Symbol;Acc:HGNC:12450]"}, {"versioned_ensembl_gene_id":"ENSG00000261098.1","gene_symbol":"AP000766.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107312132,"end":107316271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147133.15","gene_symbol":"TAF1","gene_name":"TATA-box binding protein associated factor 1 [Source:HGNC Symbol;Acc:HGNC:11535]","synonyms":"TAF2A,NSCL2,KAT4,DYT3/TAF1,DYT3,CCGS,CCG1,BA2R,TAFII250","biotype":"protein_coding","ncbi_id":"6872","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is the basal transcription factor TFIID, which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes the largest subunit of TFIID. This subunit binds to core promoter sequences encompassing the transcription start site. It also binds to activators and other transcriptional regulators, and these interactions affect the rate of transcription initiation. This subunit contains two independent protein kinase domains at the N- and C-terminals, but also possesses acetyltransferase activity and can act as a ubiquitin-activating/conjugating enzyme. Mutations in this gene result in Dystonia 3, torsion, X-linked, a dystonia-parkinsonism disorder. Alternative splicing of this gene results in multiple transcript variants. This gene is part of a complex transcription unit (TAF1/DYT3), wherein some transcript variants share exons with TAF1 as well as additional downstream DYT3 exons. [provided by RefSeq, Oct 2013]","start":71366239,"end":71532374,"strand":1,"description":"TATA-box binding protein associated factor 1 [Source:HGNC Symbol;Acc:HGNC:11535]"}, {"versioned_ensembl_gene_id":"ENSG00000183309.11","gene_symbol":"ZNF623","gene_name":"zinc finger protein 623 [Source:HGNC Symbol;Acc:HGNC:29084]","synonyms":"KIAA0628","biotype":"protein_coding","ncbi_id":"9831","summary":null,"start":143636013,"end":143656418,"strand":1,"description":"zinc finger protein 623 [Source:HGNC Symbol;Acc:HGNC:29084]"}, {"versioned_ensembl_gene_id":"ENSG00000251044.2","gene_symbol":"AC024579.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68374765,"end":68375292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070831.15","gene_symbol":"CDC42","gene_name":"cell division cycle 42 [Source:HGNC Symbol;Acc:HGNC:1736]","synonyms":"G25K,CDC42Hs","biotype":"protein_coding","ncbi_id":"998","summary":"The protein encoded by this gene is a small GTPase of the Rho-subfamily, which regulates signaling pathways that control diverse cellular functions including cell morphology, migration, endocytosis and cell cycle progression. This protein is highly similar to Saccharomyces cerevisiae Cdc 42, and is able to complement the yeast cdc42-1 mutant. The product of oncogene Dbl was reported to specifically catalyze the dissociation of GDP from this protein. This protein could regulate actin polymerization through its direct binding to Neural Wiskott-Aldrich syndrome protein (N-WASP), which subsequently activates Arp2/3 complex. Alternative splicing of this gene results in multiple transcript variants. Pseudogenes of this gene have been identified on chromosomes 3, 4, 5, 7, 8 and 20. [provided by RefSeq, Apr 2013]","start":22052627,"end":22092946,"strand":1,"description":"cell division cycle 42 [Source:HGNC Symbol;Acc:HGNC:1736]"}, {"versioned_ensembl_gene_id":"ENSG00000271428.1","gene_symbol":"AL031281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22068340,"end":22068827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105695.14","gene_symbol":"MAG","gene_name":"myelin associated glycoprotein [Source:HGNC Symbol;Acc:HGNC:6783]","synonyms":"SIGLEC4A,SIGLEC-4A,S-MAG,GMA","biotype":"protein_coding","ncbi_id":"4099","summary":"The protein encoded by this gene is a type I membrane protein and member of the immunoglobulin superfamily. It is thought to be involved in the process of myelination. It is a lectin that binds to sialylated glycoconjugates and mediates certain myelin-neuron cell-cell interactions. Three alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Nov 2010]","start":35292125,"end":35313804,"strand":1,"description":"myelin associated glycoprotein [Source:HGNC Symbol;Acc:HGNC:6783]"}, {"versioned_ensembl_gene_id":"ENSG00000005243.9","gene_symbol":"COPZ2","gene_name":"coatomer protein complex subunit zeta 2 [Source:HGNC Symbol;Acc:HGNC:19356]","synonyms":"MGC23008","biotype":"protein_coding","ncbi_id":"51226","summary":"This gene encodes a member of the adaptor complexes small subunit family. The encoded protein is a subunit of the coatomer protein complex, a seven-subunit complex that functions in the formation of COPI-type, non-clathrin-coated vesicles. COPI vesicles function in the retrograde Golgi-to-ER transport of dilysine-tagged proteins. [provided by RefSeq, Feb 2014]","start":48026167,"end":48038030,"strand":-1,"description":"coatomer protein complex subunit zeta 2 [Source:HGNC Symbol;Acc:HGNC:19356]"}, {"versioned_ensembl_gene_id":"ENSG00000227218.7","gene_symbol":"AL157935.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127934503,"end":127940952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250049.5","gene_symbol":"AC114316.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92082597,"end":92479426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165209.18","gene_symbol":"STRBP","gene_name":"spermatid perinuclear RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16462]","synonyms":"ILF3L,FLJ11307,SPNR","biotype":"protein_coding","ncbi_id":"55342","summary":null,"start":123109500,"end":123268576,"strand":-1,"description":"spermatid perinuclear RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16462]"}, {"versioned_ensembl_gene_id":"ENSG00000273859.4","gene_symbol":"RASSF7","gene_name":"Ras association domain family member 7 [Source:HGNC Symbol;Acc:HGNC:1166]","synonyms":"HRC1,HRAS1,C11orf13","biotype":"protein_coding","ncbi_id":"8045","summary":null,"start":560418,"end":564036,"strand":1,"description":"Ras association domain family member 7 [Source:HGNC Symbol;Acc:HGNC:1166]"}, {"versioned_ensembl_gene_id":"ENSG00000175202.3","gene_symbol":"HIGD2B","gene_name":"HIG1 hypoxia inducible domain family member 2B [Source:HGNC Symbol;Acc:HGNC:26984]","synonyms":"HIGD2BP","biotype":"protein_coding","ncbi_id":"123346","summary":null,"start":72675783,"end":72686149,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 2B [Source:HGNC Symbol;Acc:HGNC:26984]"}, {"versioned_ensembl_gene_id":"ENSG00000219186.2","gene_symbol":"FTH1P19","gene_name":"ferritin heavy chain 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33525]","synonyms":"FTHL19","biotype":"unprocessed_pseudogene","ncbi_id":"389844","summary":null,"start":37492021,"end":37492548,"strand":1,"description":"ferritin heavy chain 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33525]"}, {"versioned_ensembl_gene_id":"ENSG00000278068.1","gene_symbol":"AL136317.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66029264,"end":66030169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232370.1","gene_symbol":"AF241726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38479215,"end":38479913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183155.4","gene_symbol":"RABIF","gene_name":"RAB interacting factor [Source:HGNC Symbol;Acc:HGNC:9797]","synonyms":"RASGRF3,mss4","biotype":"protein_coding","ncbi_id":"5877","summary":"This gene encodes a member of the SCE4/YPT1/RAB family of small GTP-binding proteins that are involved in the regulation of intracellular vesicular transport. This protein stimulates GTP-GDP exchange in SEC4, and to a lesser extent in YPT1 and RAB3A, and may play a general role in vesicular transport. [provided by RefSeq, Oct 2011]","start":202878957,"end":202889135,"strand":-1,"description":"RAB interacting factor [Source:HGNC Symbol;Acc:HGNC:9797]"}, {"versioned_ensembl_gene_id":"ENSG00000278824.1","gene_symbol":"AC143336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71754378,"end":71756301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241942.2","gene_symbol":"RPS20P20","gene_name":"ribosomal protein S20 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36674]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271233","summary":null,"start":71895991,"end":71896330,"strand":1,"description":"ribosomal protein S20 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36674]"}, {"versioned_ensembl_gene_id":"ENSG00000118263.14","gene_symbol":"KLF7","gene_name":"Kruppel like factor 7 [Source:HGNC Symbol;Acc:HGNC:6350]","synonyms":"UKLF","biotype":"protein_coding","ncbi_id":"8609","summary":"The protein encoded by this gene is a member of the Kruppel-like transcriptional regulator family. Members in this family regulate cell proliferation, differentiation and survival and contain three C2H2 zinc fingers at the C-terminus that mediate binding to GC-rich sites. This protein may contribute to the progression of type 2 diabetes by inhibiting insulin expression and secretion in pancreatic beta-cells and by deregulating adipocytokine secretion in adipocytes. A pseudogene of this gene is located on the long arm of chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":207074137,"end":207167267,"strand":-1,"description":"Kruppel like factor 7 [Source:HGNC Symbol;Acc:HGNC:6350]"}, {"versioned_ensembl_gene_id":"ENSG00000186118.8","gene_symbol":"TEX38","gene_name":"testis expressed 38 [Source:HGNC Symbol;Acc:HGNC:29589]","synonyms":"THEG4,LOC374973,C1orf223,ATPAF1-AS1","biotype":"protein_coding","ncbi_id":"374973","summary":null,"start":46668855,"end":46673594,"strand":1,"description":"testis expressed 38 [Source:HGNC Symbol;Acc:HGNC:29589]"}, {"versioned_ensembl_gene_id":"ENSG00000270849.1","gene_symbol":"CHCHD2P3","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39587]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128110","summary":null,"start":34126973,"end":34127423,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39587]"}, {"versioned_ensembl_gene_id":"ENSG00000283329.1","gene_symbol":"FAM240B","gene_name":"family with sequence similarity 240 member B [Source:HGNC Symbol;Acc:HGNC:53430]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38694263,"end":38720428,"strand":-1,"description":"family with sequence similarity 240 member B [Source:HGNC Symbol;Acc:HGNC:53430]"}, {"versioned_ensembl_gene_id":"ENSG00000177257.2","gene_symbol":"DEFB4B","gene_name":"defensin beta 4B [Source:HGNC Symbol;Acc:HGNC:30193]","synonyms":"DEFB4P","biotype":"protein_coding","ncbi_id":"100289462","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 4, an antibiotic peptide which is locally regulated by inflammation. [provided by RefSeq, Oct 2014]","start":7414860,"end":7416863,"strand":-1,"description":"defensin beta 4B [Source:HGNC Symbol;Acc:HGNC:30193]"}, {"versioned_ensembl_gene_id":"ENSG00000173915.14","gene_symbol":"USMG5","gene_name":"up-regulated during skeletal muscle growth 5 homolog (mouse) [Source:HGNC Symbol;Acc:HGNC:30889]","synonyms":"MGC14697,DAPIT,bA792D24.4","biotype":"protein_coding","ncbi_id":"84833","summary":null,"start":103389041,"end":103396466,"strand":-1,"description":"up-regulated during skeletal muscle growth 5 homolog (mouse) [Source:HGNC Symbol;Acc:HGNC:30889]"}, {"versioned_ensembl_gene_id":"ENSG00000279972.1","gene_symbol":"AL356596.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41514972,"end":41515350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281952.1","gene_symbol":"TRBV8-1","gene_name":"T-cell receptor beta variable 8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12244]","synonyms":"TRBV81,TCRBV8S1P,TCRBV30S1P","biotype":"TR_V_pseudogene","ncbi_id":"28588","summary":null,"start":142380331,"end":142380609,"strand":1,"description":"T-cell receptor beta variable 8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12244]"}, {"versioned_ensembl_gene_id":"ENSG00000007545.15","gene_symbol":"CRAMP1","gene_name":"cramped chromatin regulator homolog 1 [Source:HGNC Symbol;Acc:HGNC:14122]","synonyms":"KIAA1426,CRAMP1L","biotype":"protein_coding","ncbi_id":"57585","summary":null,"start":1612325,"end":1677908,"strand":1,"description":"cramped chromatin regulator homolog 1 [Source:HGNC Symbol;Acc:HGNC:14122]"}, {"versioned_ensembl_gene_id":"ENSG00000261732.1","gene_symbol":"AL031708.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1632259,"end":1686715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282506.1","gene_symbol":"AC234635.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142374511,"end":142375050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196739.14","gene_symbol":"COL27A1","gene_name":"collagen type XXVII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22986]","synonyms":"MGC11337,KIAA1870,FLJ11895","biotype":"protein_coding","ncbi_id":"85301","summary":"This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014]","start":114155560,"end":114312511,"strand":1,"description":"collagen type XXVII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22986]"}, {"versioned_ensembl_gene_id":"ENSG00000127325.18","gene_symbol":"BEST3","gene_name":"bestrophin 3 [Source:HGNC Symbol;Acc:HGNC:17105]","synonyms":"VMD2L3,MGC40411,MGC13168","biotype":"protein_coding","ncbi_id":"144453","summary":"BEST3 belongs to the bestrophin family of anion channels, which includes BEST1 (MIM 607854), the gene mutant in vitelliform macular dystrophy (VMD; MIM 153700), and 2 other BEST1-like genes, BEST2 (MIM 607335) and BEST4 (MIM 607336). Bestrophins are transmembrane (TM) proteins that share a homology region containing a high content of aromatic residues, including an invariant arg-phe-pro (RFP) motif. The bestrophin genes share a conserved gene structure, with almost identical sizes of the 8 RFP-TM domain-encoding exons and highly conserved exon-intron boundaries. Each of the 4 bestrophin genes has a unique 3-prime end of variable length (Stohr et al., 2002 [PubMed 12032738]; Tsunenari et al., 2003 [PubMed 12907679]).[supplied by OMIM, Mar 2008]","start":69643360,"end":69699476,"strand":-1,"description":"bestrophin 3 [Source:HGNC Symbol;Acc:HGNC:17105]"}, {"versioned_ensembl_gene_id":"ENSG00000236242.1","gene_symbol":"MYO16-AS1","gene_name":"MYO16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39913]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885782","summary":null,"start":109163902,"end":109201483,"strand":-1,"description":"MYO16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39913]"}, {"versioned_ensembl_gene_id":"ENSG00000241411.1","gene_symbol":"AC104619.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134952259,"end":134952889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211834.1","gene_symbol":"TRAJ57","gene_name":"T-cell receptor alpha joining 57 [Source:HGNC Symbol;Acc:HGNC:12089]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28698","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22478872,"end":22478934,"strand":1,"description":"T-cell receptor alpha joining 57 [Source:HGNC Symbol;Acc:HGNC:12089]"}, {"versioned_ensembl_gene_id":"ENSG00000223959.8","gene_symbol":"AFG3L1P","gene_name":"AFG3 like matrix AAA peptidase subunit 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:314]","synonyms":"AFG3L1,AFG3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"172","summary":null,"start":89972586,"end":90002161,"strand":1,"description":"AFG3 like matrix AAA peptidase subunit 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:314]"}, {"versioned_ensembl_gene_id":"ENSG00000269959.1","gene_symbol":"SPACA6P-AS","gene_name":"SPACA6P antisense RNA [Source:HGNC Symbol;Acc:HGNC:49383]","synonyms":"LINC01129","biotype":"lincRNA","ncbi_id":"102238594","summary":null,"start":51685363,"end":51693456,"strand":-1,"description":"SPACA6P antisense RNA [Source:HGNC Symbol;Acc:HGNC:49383]"}, {"versioned_ensembl_gene_id":"ENSG00000248578.1","gene_symbol":"NPM1P21","gene_name":"nucleophosmin 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:13855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129237","summary":null,"start":56101199,"end":56102267,"strand":-1,"description":"nucleophosmin 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:13855]"}, {"versioned_ensembl_gene_id":"ENSG00000224410.1","gene_symbol":"AC097499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125823108,"end":125823315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103021.9","gene_symbol":"CCDC113","gene_name":"coiled-coil domain containing 113 [Source:HGNC Symbol;Acc:HGNC:25002]","synonyms":"HSPC065,DKFZp434N1418","biotype":"protein_coding","ncbi_id":"29070","summary":null,"start":58231157,"end":58283836,"strand":1,"description":"coiled-coil domain containing 113 [Source:HGNC Symbol;Acc:HGNC:25002]"}, {"versioned_ensembl_gene_id":"ENSG00000279811.1","gene_symbol":"AC093330.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77002849,"end":77006846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220349.4","gene_symbol":"Z85996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36737050,"end":36737986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147166.10","gene_symbol":"ITGB1BP2","gene_name":"integrin subunit beta 1 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6154]","synonyms":"CHORDC3","biotype":"protein_coding","ncbi_id":"26548","summary":"This gene encodes a protein with two cysteine and histidine-rich (CHORD) domains, PXXP motifs, YXXI/P motifs, putative SH2 and SH3 domain binding motifs, and an acidic region at the C-terminus that can bind calcium. Two hybrid analysis showed that this protein interacts with the cytoplasmic domain of the beta 1 integrin subunit and is thought to act as a chaperone protein. Studies in the mouse ortholog of this gene indicate that absence of this gene in mouse results in failed cardiac hypertrophy in response to mechanical stress. Alternative splicing results in multiple transcript variants encoding different isoforms, including an isoform that lacks several domains, including one of the CHORD domains. [provided by RefSeq, May 2017]","start":71301734,"end":71305371,"strand":1,"description":"integrin subunit beta 1 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6154]"}, {"versioned_ensembl_gene_id":"ENSG00000148798.10","gene_symbol":"INA","gene_name":"internexin neuronal intermediate filament protein alpha [Source:HGNC Symbol;Acc:HGNC:6057]","synonyms":"NF-66,NEF5","biotype":"protein_coding","ncbi_id":"9118","summary":"Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene is a member of the intermediate filament family and is involved in the morphogenesis of neurons. [provided by RefSeq, Jun 2009]","start":103277163,"end":103290351,"strand":1,"description":"internexin neuronal intermediate filament protein alpha [Source:HGNC Symbol;Acc:HGNC:6057]"}, {"versioned_ensembl_gene_id":"ENSG00000229256.1","gene_symbol":"ST13P13","gene_name":"ST13, Hsp70 interacting protein pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38788]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401648","summary":null,"start":103215709,"end":103216800,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38788]"}, {"versioned_ensembl_gene_id":"ENSG00000228444.2","gene_symbol":"AL137244.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75631271,"end":75632135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183111.11","gene_symbol":"ARHGEF37","gene_name":"Rho guanine nucleotide exchange factor 37 [Source:HGNC Symbol;Acc:HGNC:34430]","synonyms":"FLJ41603","biotype":"protein_coding","ncbi_id":"389337","summary":null,"start":149551947,"end":149634968,"strand":1,"description":"Rho guanine nucleotide exchange factor 37 [Source:HGNC Symbol;Acc:HGNC:34430]"}, {"versioned_ensembl_gene_id":"ENSG00000261182.1","gene_symbol":"AL596211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188218400,"end":188220676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233922.2","gene_symbol":"LINC01694","gene_name":"long intergenic non-protein coding RNA 1694 [Source:HGNC Symbol;Acc:HGNC:52481]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372840","summary":null,"start":45593654,"end":45603056,"strand":1,"description":"long intergenic non-protein coding RNA 1694 [Source:HGNC Symbol;Acc:HGNC:52481]"}, {"versioned_ensembl_gene_id":"ENSG00000261286.1","gene_symbol":"ATP2C2-AS1","gene_name":"ATP2C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53167]","synonyms":"RP11-517C16.2-001","biotype":"antisense_RNA","ncbi_id":"105371374","summary":null,"start":84459259,"end":84467361,"strand":-1,"description":"ATP2C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53167]"}, {"versioned_ensembl_gene_id":"ENSG00000183423.11","gene_symbol":"LRIT3","gene_name":"leucine rich repeat, Ig-like and transmembrane domains 3 [Source:HGNC Symbol;Acc:HGNC:24783]","synonyms":"FLJ44691,FIGLER4,CSNB1F","biotype":"protein_coding","ncbi_id":"345193","summary":"This gene encodes a protein that has a fibronectin type III domain and a C-terminal transmembrane domain, as well as a leucine-rich repeat domain and immunoglobulin-like domain near the N-terminus. The encoded protein may regulate fibroblast growth factor receptors and affect the modification of these receptors, which are glycosylated differently in the Golgi and endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night blindness, type 1F. [provided by RefSeq, May 2013]","start":109848202,"end":109872315,"strand":1,"description":"leucine rich repeat, Ig-like and transmembrane domains 3 [Source:HGNC Symbol;Acc:HGNC:24783]"}, {"versioned_ensembl_gene_id":"ENSG00000273217.1","gene_symbol":"AC008695.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":131425891,"end":131796983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186260.16","gene_symbol":"MKL2","gene_name":"MKL1/myocardin like 2 [Source:HGNC Symbol;Acc:HGNC:29819]","synonyms":"MRTF-B,FLJ31823","biotype":"protein_coding","ncbi_id":"57496","summary":null,"start":14071321,"end":14266773,"strand":1,"description":"MKL1/myocardin like 2 [Source:HGNC Symbol;Acc:HGNC:29819]"}, {"versioned_ensembl_gene_id":"ENSG00000262529.1","gene_symbol":"AC130650.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14191820,"end":14200277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187140.5","gene_symbol":"FOXD3","gene_name":"forkhead box D3 [Source:HGNC Symbol;Acc:HGNC:3804]","synonyms":"HFH2,Genesis","biotype":"protein_coding","ncbi_id":"27022","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. Mutations in this gene cause autoimmune susceptibility 1. [provided by RefSeq, Nov 2008]","start":63323041,"end":63325126,"strand":1,"description":"forkhead box D3 [Source:HGNC Symbol;Acc:HGNC:3804]"}, {"versioned_ensembl_gene_id":"ENSG00000240522.1","gene_symbol":"RPL7AP10","gene_name":"ribosomal protein L7a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:32433]","synonyms":"RPL7AP68","biotype":"processed_pseudogene","ncbi_id":"161406","summary":null,"start":21149648,"end":21150438,"strand":-1,"description":"ribosomal protein L7a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:32433]"}, {"versioned_ensembl_gene_id":"ENSG00000235319.1","gene_symbol":"AC012360.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105324210,"end":105330529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148925.10","gene_symbol":"BTBD10","gene_name":"BTB domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21445]","synonyms":"GMRP-1,MGC13007,GMRP1","biotype":"protein_coding","ncbi_id":"84280","summary":null,"start":13388001,"end":13463297,"strand":-1,"description":"BTB domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21445]"}, {"versioned_ensembl_gene_id":"ENSG00000279677.1","gene_symbol":"AL162377.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51921251,"end":51921587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105976.14","gene_symbol":"MET","gene_name":"MET proto-oncogene, receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7029]","synonyms":"RCCP2,HGFR,DFNB97","biotype":"protein_coding","ncbi_id":"4233","summary":"This gene encodes a member of the receptor tyrosine kinase family of proteins and the product of the proto-oncogene MET. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that are linked via disulfide bonds to form the mature receptor. Further processing of the beta subunit results in the formation of the M10 peptide, which has been shown to reduce lung fibrosis. Binding of its ligand, hepatocyte growth factor, induces dimerization and activation of the receptor, which plays a role in cellular survival, embryogenesis, and cellular migration and invasion. Mutations in this gene are associated with papillary renal cell carcinoma, hepatocellular carcinoma, and various head and neck cancers. Amplification and overexpression of this gene are also associated with multiple human cancers. [provided by RefSeq, May 2016]","start":116672390,"end":116798386,"strand":1,"description":"MET proto-oncogene, receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7029]"}, {"versioned_ensembl_gene_id":"ENSG00000171448.8","gene_symbol":"ZBTB26","gene_name":"zinc finger and BTB domain containing 26 [Source:HGNC Symbol;Acc:HGNC:23383]","synonyms":"ZNF481","biotype":"protein_coding","ncbi_id":"57684","summary":null,"start":122915566,"end":122931500,"strand":-1,"description":"zinc finger and BTB domain containing 26 [Source:HGNC Symbol;Acc:HGNC:23383]"}, {"versioned_ensembl_gene_id":"ENSG00000213025.2","gene_symbol":"COX20P1","gene_name":"COX20, cytochrome c oxidase assembly factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31435]","synonyms":"FAM36B,bA119F7.2","biotype":"processed_pseudogene","ncbi_id":"100507102","summary":null,"start":68632371,"end":68632727,"strand":1,"description":"COX20, cytochrome c oxidase assembly factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31435]"}, {"versioned_ensembl_gene_id":"ENSG00000276992.1","gene_symbol":"AC096577.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104996900,"end":104997052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251473.2","gene_symbol":"AC004069.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105102891,"end":105104004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188086.13","gene_symbol":"PRSS45","gene_name":"protease, serine 45 [Source:HGNC Symbol;Acc:HGNC:30717]","synonyms":"TESSP5","biotype":"protein_coding","ncbi_id":"377047","summary":null,"start":46742092,"end":46744755,"strand":-1,"description":"protease, serine 45 [Source:HGNC Symbol;Acc:HGNC:30717]"}, {"versioned_ensembl_gene_id":"ENSG00000225345.3","gene_symbol":"SNX18P3","gene_name":"sorting nexin 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39611]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100418975","summary":null,"start":38566260,"end":38568211,"strand":-1,"description":"sorting nexin 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39611]"}, {"versioned_ensembl_gene_id":"ENSG00000284648.1","gene_symbol":"AC097493.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9532429,"end":9532647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186130.4","gene_symbol":"ZBTB6","gene_name":"zinc finger and BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:16764]","synonyms":"ZNF482,ZID","biotype":"protein_coding","ncbi_id":"10773","summary":null,"start":122908056,"end":122913330,"strand":-1,"description":"zinc finger and BTB domain containing 6 [Source:HGNC Symbol;Acc:HGNC:16764]"}, {"versioned_ensembl_gene_id":"ENSG00000268521.1","gene_symbol":"VN1R83P","gene_name":"vomeronasal 1 receptor 83 pseudogene [Source:HGNC Symbol;Acc:HGNC:37403]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312828","summary":null,"start":21289554,"end":21289998,"strand":-1,"description":"vomeronasal 1 receptor 83 pseudogene [Source:HGNC Symbol;Acc:HGNC:37403]"}, {"versioned_ensembl_gene_id":"ENSG00000141446.10","gene_symbol":"ESCO1","gene_name":"establishment of sister chromatid cohesion N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24645]","synonyms":"KIAA1911,ESO1,EFO1","biotype":"protein_coding","ncbi_id":"114799","summary":"ESCO1 belongs to a conserved family of acetyltransferases involved in sister chromatid cohesion (Hou and Zou, 2005 [PubMed 15958495]).[supplied by OMIM, Mar 2008]","start":21529281,"end":21600884,"strand":-1,"description":"establishment of sister chromatid cohesion N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24645]"}, {"versioned_ensembl_gene_id":"ENSG00000282543.1","gene_symbol":"AC234635.4","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142362570,"end":142363134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254522.1","gene_symbol":"AP001767.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83040806,"end":83041403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145287.10","gene_symbol":"PLAC8","gene_name":"placenta specific 8 [Source:HGNC Symbol;Acc:HGNC:19254]","synonyms":"onzin,C15","biotype":"protein_coding","ncbi_id":"51316","summary":null,"start":83090048,"end":83137075,"strand":-1,"description":"placenta specific 8 [Source:HGNC Symbol;Acc:HGNC:19254]"}, {"versioned_ensembl_gene_id":"ENSG00000234479.2","gene_symbol":"AP1B1P1","gene_name":"adaptor related protein complex 1 beta 1 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:297]","synonyms":"dJ127L4.2,ADTB1L1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"23782","summary":null,"start":32121977,"end":32133469,"strand":1,"description":"adaptor related protein complex 1 beta 1 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:297]"}, {"versioned_ensembl_gene_id":"ENSG00000257509.1","gene_symbol":"AC073487.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55761550,"end":55762628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223824.1","gene_symbol":"AC019178.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189917254,"end":189917758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255143.1","gene_symbol":"AP000879.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":70129297,"end":70149623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140443.13","gene_symbol":"IGF1R","gene_name":"insulin like growth factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:5465]","synonyms":"MGC18216,JTK13,IGFR,IGFIR,CD221","biotype":"protein_coding","ncbi_id":"3480","summary":"This receptor binds insulin-like growth factor with a high affinity. It has tyrosine kinase activity. The insulin-like growth factor I receptor plays a critical role in transformation events. Cleavage of the precursor generates alpha and beta subunits. It is highly overexpressed in most malignant tissues where it functions as an anti-apoptotic agent by enhancing cell survival. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":98648971,"end":98964530,"strand":1,"description":"insulin like growth factor 1 receptor [Source:HGNC Symbol;Acc:HGNC:5465]"}, {"versioned_ensembl_gene_id":"ENSG00000104880.17","gene_symbol":"ARHGEF18","gene_name":"Rho/Rac guanine nucleotide exchange factor 18 [Source:HGNC Symbol;Acc:HGNC:17090]","synonyms":"P114-RhoGEF,MGC15913,KIAA0521","biotype":"protein_coding","ncbi_id":"23370","summary":"Rho GTPases are GTP binding proteins that regulate a wide spectrum of cellular functions. These cellular processes include cytoskeletal rearrangements, gene transcription, cell growth and motility. Activation of Rho GTPases is under the direct control of guanine nucleotide exchange factors (GEFs). The protein encoded by this gene is a guanine nucleotide exchange factor and belongs to the Rho GTPase GEF family. Family members share a common feature, a Dbl (DH) homology domain followed by a pleckstrin (PH) homology domain. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Nov 2018]","start":7395113,"end":7472477,"strand":1,"description":"Rho/Rac guanine nucleotide exchange factor 18 [Source:HGNC Symbol;Acc:HGNC:17090]"}, {"versioned_ensembl_gene_id":"ENSG00000263264.1","gene_symbol":"AC119396.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7348943,"end":7383385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270000.1","gene_symbol":"AC005479.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74471930,"end":74472360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228943.1","gene_symbol":"AL137792.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28109739,"end":28110298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248933.2","gene_symbol":"USP17L22","gene_name":"ubiquitin specific peptidase 17-like family member 22 [Source:HGNC Symbol;Acc:HGNC:44450]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287513","summary":null,"start":9267619,"end":9269570,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 22 [Source:HGNC Symbol;Acc:HGNC:44450]"}, {"versioned_ensembl_gene_id":"ENSG00000279140.1","gene_symbol":"AL590326.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":104815449,"end":104815753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223739.1","gene_symbol":"AC007389.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65511771,"end":65512076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141384.12","gene_symbol":"TAF4B","gene_name":"TATA-box binding protein associated factor 4b [Source:HGNC Symbol;Acc:HGNC:11538]","synonyms":"TAFII105,TAF2C2","biotype":"protein_coding","ncbi_id":"6875","summary":"TATA binding protein (TBP) and TBP-associated factors (TAFs) participate in the formation of the TFIID protein complex, which is involved in initiation of transcription of genes by RNA polymerase II. This gene encodes a cell type-specific TAF that may be responsible for mediating transcription by a subset of activators in B cells. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":26225936,"end":26391685,"strand":1,"description":"TATA-box binding protein associated factor 4b [Source:HGNC Symbol;Acc:HGNC:11538]"}, {"versioned_ensembl_gene_id":"ENSG00000281469.1","gene_symbol":"AC019226.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":148044380,"end":148044894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107816.17","gene_symbol":"LZTS2","gene_name":"leucine zipper tumor suppressor 2 [Source:HGNC Symbol;Acc:HGNC:29381]","synonyms":"LAPSER1,KIAA1813","biotype":"protein_coding","ncbi_id":"84445","summary":"The protein encoded by this gene belongs to the leucine zipper tumor suppressor family of proteins, which function in transcription regulation and cell cycle control. This family member can repress beta-catenin-mediated transcriptional activation and is a negative regulator of the Wnt signaling pathway. It negatively regulates microtubule severing at centrosomes, and is necessary for central spindle formation and cytokinesis completion. It is implicated in cancer, where it may inhibit cell proliferation and decrease susceptibility to tumor development. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":100996618,"end":101007836,"strand":1,"description":"leucine zipper tumor suppressor 2 [Source:HGNC Symbol;Acc:HGNC:29381]"}, {"versioned_ensembl_gene_id":"ENSG00000231006.1","gene_symbol":"RPL7P32","gene_name":"ribosomal protein L7 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35692]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130892","summary":null,"start":108510233,"end":108510976,"strand":1,"description":"ribosomal protein L7 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:35692]"}, {"versioned_ensembl_gene_id":"ENSG00000267443.2","gene_symbol":"AC010641.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":397589,"end":399173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251555.1","gene_symbol":"AC096711.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131930031,"end":131975952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184139.8","gene_symbol":"RPL7AP28","gene_name":"ribosomal protein L7a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35656]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271209","summary":null,"start":131857343,"end":131857913,"strand":-1,"description":"ribosomal protein L7a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35656]"}, {"versioned_ensembl_gene_id":"ENSG00000261064.1","gene_symbol":"LINC02256","gene_name":"long intergenic non-protein coding RNA 2256 [Source:HGNC Symbol;Acc:HGNC:53157]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996255","summary":null,"start":32536047,"end":32587613,"strand":1,"description":"long intergenic non-protein coding RNA 2256 [Source:HGNC Symbol;Acc:HGNC:53157]"}, {"versioned_ensembl_gene_id":"ENSG00000164080.13","gene_symbol":"RAD54L2","gene_name":"RAD54 like 2 (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:29123]","synonyms":"KIAA0809,ARIP4,SRISNF2L","biotype":"protein_coding","ncbi_id":"23132","summary":null,"start":51541144,"end":51668667,"strand":1,"description":"RAD54 like 2 (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:29123]"}, {"versioned_ensembl_gene_id":"ENSG00000115107.19","gene_symbol":"STEAP3","gene_name":"STEAP3 metalloreductase [Source:HGNC Symbol;Acc:HGNC:24592]","synonyms":"TSAP6,STMP3,dudlin-2","biotype":"protein_coding","ncbi_id":"55240","summary":"This gene encodes a multipass membrane protein that functions as an iron transporter. The encoded protein can reduce both iron (Fe3+) and copper (Cu2+) cations. This protein may mediate downstream responses to p53, including promoting apoptosis. Deficiency in this gene can cause anemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":119223831,"end":119265652,"strand":1,"description":"STEAP3 metalloreductase [Source:HGNC Symbol;Acc:HGNC:24592]"}, {"versioned_ensembl_gene_id":"ENSG00000269779.1","gene_symbol":"AC010329.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20691336,"end":20697615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268416.1","gene_symbol":"AC010329.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20746923,"end":20755250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271704.1","gene_symbol":"BNIP3P20","gene_name":"BCL2 interacting protein 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49700]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421705","summary":null,"start":20351502,"end":20352079,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49700]"}, {"versioned_ensembl_gene_id":"ENSG00000184389.9","gene_symbol":"A3GALT2","gene_name":"alpha 1,3-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:30005]","synonyms":"IGBS3S,IGB3S,A3GALT2P","biotype":"protein_coding","ncbi_id":"127550","summary":null,"start":33306766,"end":33321098,"strand":-1,"description":"alpha 1,3-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:30005]"}, {"versioned_ensembl_gene_id":"ENSG00000259094.1","gene_symbol":"AC013457.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118949306,"end":118952983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182253.14","gene_symbol":"SYNM","gene_name":"synemin [Source:HGNC Symbol;Acc:HGNC:24466]","synonyms":"SYN,KIAA0353,DMN","biotype":"protein_coding","ncbi_id":"23336","summary":"The protein encoded by this gene is an intermediate filament (IF) family member. IF proteins are cytoskeletal proteins that confer resistance to mechanical stress and are encoded by a dispersed multigene family. This protein has been found to form a linkage between desmin, which is a subunit of the IF network, and the extracellular matrix, and provides an important structural support in muscle. Two alternatively spliced variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":99098217,"end":99135593,"strand":1,"description":"synemin [Source:HGNC Symbol;Acc:HGNC:24466]"}, {"versioned_ensembl_gene_id":"ENSG00000260095.1","gene_symbol":"AC106820.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2452581,"end":2452977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279847.3","gene_symbol":"C8orf87","gene_name":"chromosome 8 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:42974]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389676","summary":null,"start":93134095,"end":93166850,"strand":-1,"description":"chromosome 8 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:42974]"}, {"versioned_ensembl_gene_id":"ENSG00000163612.10","gene_symbol":"FAM86KP","gene_name":"family with sequence similarity 86 member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:44098]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287013","summary":null,"start":9153296,"end":9165451,"strand":1,"description":"family with sequence similarity 86 member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:44098]"}, {"versioned_ensembl_gene_id":"ENSG00000239827.8","gene_symbol":"SUGT1P3","gene_name":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20513]","synonyms":"SUGT1L1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"283507","summary":null,"start":40882577,"end":40921774,"strand":-1,"description":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20513]"}, {"versioned_ensembl_gene_id":"ENSG00000253480.1","gene_symbol":"AC122713.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180085717,"end":180087038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131620.17","gene_symbol":"ANO1","gene_name":"anoctamin 1 [Source:HGNC Symbol;Acc:HGNC:21625]","synonyms":"TMEM16A,TAOS2,ORAOV2,DOG1,FLJ10261","biotype":"protein_coding","ncbi_id":"55107","summary":null,"start":70078302,"end":70189528,"strand":1,"description":"anoctamin 1 [Source:HGNC Symbol;Acc:HGNC:21625]"}, {"versioned_ensembl_gene_id":"ENSG00000249272.1","gene_symbol":"UNC93B8","gene_name":"unc-93 homolog B8 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:44037]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100887748","summary":null,"start":8959628,"end":8963981,"strand":1,"description":"unc-93 homolog B8 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:44037]"}, {"versioned_ensembl_gene_id":"ENSG00000171459.4","gene_symbol":"OR1L6","gene_name":"olfactory receptor family 1 subfamily L member 6 [Source:HGNC Symbol;Acc:HGNC:8218]","synonyms":"OR1L7","biotype":"protein_coding","ncbi_id":"392390","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122742303,"end":122750783,"strand":1,"description":"olfactory receptor family 1 subfamily L member 6 [Source:HGNC Symbol;Acc:HGNC:8218]"}, {"versioned_ensembl_gene_id":"ENSG00000137200.12","gene_symbol":"CMTR1","gene_name":"cap methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21077]","synonyms":"MTr1,KIAA0082,ISG95,FTSJD2","biotype":"protein_coding","ncbi_id":"23070","summary":null,"start":37433219,"end":37482827,"strand":1,"description":"cap methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21077]"}, {"versioned_ensembl_gene_id":"ENSG00000258272.1","gene_symbol":"AC007513.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96422326,"end":96485442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158716.8","gene_symbol":"DUSP23","gene_name":"dual specificity phosphatase 23 [Source:HGNC Symbol;Acc:HGNC:21480]","synonyms":"DUSP25,FLJ20442","biotype":"protein_coding","ncbi_id":"54935","summary":null,"start":159780932,"end":159782543,"strand":1,"description":"dual specificity phosphatase 23 [Source:HGNC Symbol;Acc:HGNC:21480]"}, {"versioned_ensembl_gene_id":"ENSG00000259502.1","gene_symbol":"AL132640.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67610986,"end":67613864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187942.11","gene_symbol":"LDLRAD2","gene_name":"low density lipoprotein receptor class A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32071]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401944","summary":null,"start":21812265,"end":21825221,"strand":1,"description":"low density lipoprotein receptor class A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:32071]"}, {"versioned_ensembl_gene_id":"ENSG00000198931.10","gene_symbol":"APRT","gene_name":"adenine phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353","summary":"Adenine phosphoribosyltransferase belongs to the purine/pyrimidine phosphoribosyltransferase family. A conserved feature of this gene is the distribution of CpG dinucleotides. This enzyme catalyzes the formation of AMP and inorganic pyrophosphate from adenine and 5-phosphoribosyl-1-pyrophosphate (PRPP). It also produces adenine as a by-product of the polyamine biosynthesis pathway. A homozygous deficiency in this enzyme causes 2,8-dihydroxyadenine urolithiasis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":88809339,"end":88811944,"strand":-1,"description":"adenine phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:626]"}, {"versioned_ensembl_gene_id":"ENSG00000229191.1","gene_symbol":"AL358473.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201023949,"end":201028792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282419.2","gene_symbol":"TEX13D","gene_name":"TEX13 family member D [Source:HGNC Symbol;Acc:HGNC:52278]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132015","summary":null,"start":124246249,"end":124336862,"strand":1,"description":"TEX13 family member D [Source:HGNC Symbol;Acc:HGNC:52278]"}, {"versioned_ensembl_gene_id":"ENSG00000145506.13","gene_symbol":"NKD2","gene_name":"naked cuticle homolog 2 [Source:HGNC Symbol;Acc:HGNC:17046]","synonyms":"Naked2","biotype":"protein_coding","ncbi_id":"85409","summary":"This gene encodes a member of a family of proteins that function as negative regulators of Wnt receptor signaling through interaction with Dishevelled family members. The encoded protein participates in the delivery of transforming growth factor alpha-containing vesicles to the cell membrane. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":1008829,"end":1038943,"strand":1,"description":"naked cuticle homolog 2 [Source:HGNC Symbol;Acc:HGNC:17046]"}, {"versioned_ensembl_gene_id":"ENSG00000123349.13","gene_symbol":"PFDN5","gene_name":"prefoldin subunit 5 [Source:HGNC Symbol;Acc:HGNC:8869]","synonyms":"PFD5,MM-1","biotype":"protein_coding","ncbi_id":"5204","summary":"This gene encodes a member of the prefoldin alpha subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. The encoded protein may also repress the transcriptional activity of the proto-oncogene c-Myc. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":53295291,"end":53299450,"strand":1,"description":"prefoldin subunit 5 [Source:HGNC Symbol;Acc:HGNC:8869]"}, {"versioned_ensembl_gene_id":"ENSG00000140391.14","gene_symbol":"TSPAN3","gene_name":"tetraspanin 3 [Source:HGNC Symbol;Acc:HGNC:17752]","synonyms":"TM4SF8,TM4-A,TSPAN-3","biotype":"protein_coding","ncbi_id":"10099","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. The use of alternate polyadenylation sites has been found for this gene. Multiple alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Dec 2009]","start":77041404,"end":77083984,"strand":-1,"description":"tetraspanin 3 [Source:HGNC Symbol;Acc:HGNC:17752]"}, {"versioned_ensembl_gene_id":"ENSG00000228164.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33032837,"end":33036373,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000167822.2","gene_symbol":"OR8J3","gene_name":"olfactory receptor family 8 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:15312]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81168","summary":null,"start":56134721,"end":56140201,"strand":-1,"description":"olfactory receptor family 8 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:15312]"}, {"versioned_ensembl_gene_id":"ENSG00000067900.7","gene_symbol":"ROCK1","gene_name":"Rho associated coiled-coil containing protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:10251]","synonyms":"p160ROCK","biotype":"protein_coding","ncbi_id":"6093","summary":"This gene encodes a protein serine/threonine kinase that is activated when bound to the GTP-bound form of Rho. The small GTPase Rho regulates formation of focal adhesions and stress fibers of fibroblasts, as well as adhesion and aggregation of platelets and lymphocytes by shuttling between the inactive GDP-bound form and the active GTP-bound form. Rho is also essential in cytokinesis and plays a role in transcriptional activation by serum response factor. This protein, a downstream effector of Rho, phosphorylates and activates LIM kinase, which in turn, phosphorylates cofilin, inhibiting its actin-depolymerizing activity. A pseudogene, related to this gene, is also located on chromosome 18. [provided by RefSeq, Aug 2015]","start":20946906,"end":21111851,"strand":-1,"description":"Rho associated coiled-coil containing protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:10251]"}, {"versioned_ensembl_gene_id":"ENSG00000152213.3","gene_symbol":"ARL11","gene_name":"ADP ribosylation factor like GTPase 11 [Source:HGNC Symbol;Acc:HGNC:24046]","synonyms":"FLJ33930,ARLTS1","biotype":"protein_coding","ncbi_id":"115761","summary":"This gene encodes a tumor suppressor related to the ADP-ribosylation factor (ARF) family of proteins. The encoded protein may play a role in apoptosis in a caspase-dependent manner. Polymorphisms in this gene have been associated with some familial cancers. [provided by RefSeq, May 2010]","start":49628299,"end":49633872,"strand":1,"description":"ADP ribosylation factor like GTPase 11 [Source:HGNC Symbol;Acc:HGNC:24046]"}, {"versioned_ensembl_gene_id":"ENSG00000231723.1","gene_symbol":"AC018880.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103623630,"end":103623830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279441.1","gene_symbol":"Z92544.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":678645,"end":679061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130544.11","gene_symbol":"ZNF557","gene_name":"zinc finger protein 557 [Source:HGNC Symbol;Acc:HGNC:28632]","synonyms":"MGC4054","biotype":"protein_coding","ncbi_id":"79230","summary":null,"start":7069444,"end":7087968,"strand":1,"description":"zinc finger protein 557 [Source:HGNC Symbol;Acc:HGNC:28632]"}, {"versioned_ensembl_gene_id":"ENSG00000204287.13","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32439842,"end":32445046,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000238143.1","gene_symbol":"AL161631.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101125436,"end":101125921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267625.1","gene_symbol":"AC015911.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35561539,"end":35562077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242850.3","gene_symbol":"RPL23AP68","gene_name":"ribosomal protein L23a pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:35489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130555","summary":null,"start":87169985,"end":87170429,"strand":-1,"description":"ribosomal protein L23a pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:35489]"}, {"versioned_ensembl_gene_id":"ENSG00000176230.5","gene_symbol":"OR4K17","gene_name":"olfactory receptor family 4 subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:15355]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390436","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20110739,"end":20122199,"strand":1,"description":"olfactory receptor family 4 subfamily K member 17 [Source:HGNC Symbol;Acc:HGNC:15355]"}, {"versioned_ensembl_gene_id":"ENSG00000258641.1","gene_symbol":"OR4T1P","gene_name":"olfactory receptor family 4 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15360]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390435","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20093353,"end":20094263,"strand":1,"description":"olfactory receptor family 4 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15360]"}, {"versioned_ensembl_gene_id":"ENSG00000103269.13","gene_symbol":"RHBDL1","gene_name":"rhomboid like 1 [Source:HGNC Symbol;Acc:HGNC:10007]","synonyms":"RRP,RHBDL","biotype":"protein_coding","ncbi_id":"9028","summary":"This gene encodes a protein similar to Rhomboid in Drosophila which is involved in signalling in the Spitz/epidermal growth factor receptor/mitogen-activated protein kinase pathway. The Rhomboid family of proteins consists of intramembrane serine proteases containing several transmembrane domains. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":675666,"end":678268,"strand":1,"description":"rhomboid like 1 [Source:HGNC Symbol;Acc:HGNC:10007]"}, {"versioned_ensembl_gene_id":"ENSG00000276397.1","gene_symbol":"LINC01879","gene_name":"long intergenic non-protein coding RNA 1879 [Source:HGNC Symbol;Acc:HGNC:52698]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400661","summary":null,"start":76690029,"end":76693636,"strand":1,"description":"long intergenic non-protein coding RNA 1879 [Source:HGNC Symbol;Acc:HGNC:52698]"}, {"versioned_ensembl_gene_id":"ENSG00000237813.3","gene_symbol":"AC002066.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116238260,"end":116499465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246323.2","gene_symbol":"AC113382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138032774,"end":138037266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275786.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816499,"end":54830812,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000120800.4","gene_symbol":"UTP20","gene_name":"UTP20, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:17897]","synonyms":"DRIM,1A6/DRIM","biotype":"protein_coding","ncbi_id":"27340","summary":"UTP20 is a component of the U3 small nucleolar RNA (snoRNA) (SNORD3A; MIM 180710) protein complex (U3 snoRNP) and is involved in 18S rRNA processing (Wang et al., 2007 [PubMed 17498821]).[supplied by OMIM, Jun 2009]","start":101280109,"end":101386616,"strand":1,"description":"UTP20, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:17897]"}, {"versioned_ensembl_gene_id":"ENSG00000276148.1","gene_symbol":"AC084824.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32725248,"end":32725660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197594.11","gene_symbol":"ENPP1","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:3356]","synonyms":"PDNP1,PCA1,PC-1,NPPS,M6S1","biotype":"protein_coding","ncbi_id":"5167","summary":"This gene is a member of the ecto-nucleotide pyrophosphatase/phosphodiesterase (ENPP) family. The encoded protein is a type II transmembrane glycoprotein comprising two identical disulfide-bonded subunits. This protein has broad specificity and cleaves a variety of substrates, including phosphodiester bonds of nucleotides and nucleotide sugars and pyrophosphate bonds of nucleotides and nucleotide sugars. This protein may function to hydrolyze nucleoside 5' triphosphates to their corresponding monophosphates and may also hydrolyze diadenosine polyphosphates. Mutations in this gene have been associated with 'idiopathic' infantile arterial calcification, ossification of the posterior longitudinal ligament of the spine (OPLL), and insulin resistance. [provided by RefSeq, Jul 2008]","start":131808016,"end":131895155,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:3356]"}, {"versioned_ensembl_gene_id":"ENSG00000274523.4","gene_symbol":"RCC1L","gene_name":"RCC1 like [Source:HGNC Symbol;Acc:HGNC:14948]","synonyms":"WBSCR16","biotype":"protein_coding","ncbi_id":"81554","summary":"This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":75027122,"end":75074228,"strand":-1,"description":"RCC1 like [Source:HGNC Symbol;Acc:HGNC:14948]"}, {"versioned_ensembl_gene_id":"ENSG00000224702.1","gene_symbol":"AL390730.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165210627,"end":165213090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279733.1","gene_symbol":"AP001642.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88165575,"end":88167691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279926.1","gene_symbol":"AL138831.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3982673,"end":3984130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254683.1","gene_symbol":"SNRPCP6","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49821]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310856","summary":null,"start":7143632,"end":7143841,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49821]"}, {"versioned_ensembl_gene_id":"ENSG00000259478.2","gene_symbol":"AC024651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97982509,"end":97991142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232054.1","gene_symbol":"NPM1P34","gene_name":"nucleophosmin 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:45213]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128410","summary":null,"start":124280530,"end":124281422,"strand":1,"description":"nucleophosmin 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:45213]"}, {"versioned_ensembl_gene_id":"ENSG00000140450.8","gene_symbol":"ARRDC4","gene_name":"arrestin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28087]","synonyms":"FLJ36045","biotype":"protein_coding","ncbi_id":"91947","summary":null,"start":97960698,"end":97973838,"strand":1,"description":"arrestin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28087]"}, {"versioned_ensembl_gene_id":"ENSG00000231801.2","gene_symbol":"ANP32BP2","gene_name":"acidic nuclear phosphoprotein 32 family member B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130708","summary":null,"start":44651835,"end":44652379,"strand":1,"description":"acidic nuclear phosphoprotein 32 family member B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38552]"}, {"versioned_ensembl_gene_id":"ENSG00000230079.1","gene_symbol":"STK24P1","gene_name":"serine/threonine kinase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421784","summary":null,"start":136295690,"end":136300298,"strand":-1,"description":"serine/threonine kinase 24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50360]"}, {"versioned_ensembl_gene_id":"ENSG00000259870.1","gene_symbol":"AC024651.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97876289,"end":97878386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198231.12","gene_symbol":"DDX42","gene_name":"DEAD-box helicase 42 [Source:HGNC Symbol;Acc:HGNC:18676]","synonyms":"SF3B8,SF3b125,RNAHP,RHELP","biotype":"protein_coding","ncbi_id":"11325","summary":"This gene encodes a member of the Asp-Glu-Ala-Asp (DEAD) box protein family. Members of this protein family are putative RNA helicases, and are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":63773603,"end":63819317,"strand":1,"description":"DEAD-box helicase 42 [Source:HGNC Symbol;Acc:HGNC:18676]"}, {"versioned_ensembl_gene_id":"ENSG00000274070.1","gene_symbol":"CASTOR2","gene_name":"cytosolic arginine sensor for mTORC1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:37073]","synonyms":"GATSL1,GATSL2","biotype":"protein_coding","ncbi_id":"729438","summary":null,"start":74964818,"end":75024798,"strand":1,"description":"cytosolic arginine sensor for mTORC1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:37073]"}, {"versioned_ensembl_gene_id":"ENSG00000217477.2","gene_symbol":"AL450346.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63193072,"end":63193630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204703.5","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR2B3P,OR6-4","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086208,"end":29087313,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000117448.13","gene_symbol":"AKR1A1","gene_name":"aldo-keto reductase family 1 member A1 [Source:HGNC Symbol;Acc:HGNC:380]","synonyms":"DD3,ALR","biotype":"protein_coding","ncbi_id":"10327","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. This member, also known as aldehyde reductase, is involved in the reduction of biogenic and xenobiotic aldehydes and is present in virtually every tissue. Multiple alternatively spliced transcript variants of this gene exist, all encoding the same protein. [provided by RefSeq, Jan 2011]","start":45550543,"end":45570049,"strand":1,"description":"aldo-keto reductase family 1 member A1 [Source:HGNC Symbol;Acc:HGNC:380]"}, {"versioned_ensembl_gene_id":"ENSG00000251635.1","gene_symbol":"LINC02278","gene_name":"long intergenic non-protein coding RNA 2278 [Source:HGNC Symbol;Acc:HGNC:53194]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374411","summary":null,"start":38564003,"end":38570671,"strand":1,"description":"long intergenic non-protein coding RNA 2278 [Source:HGNC Symbol;Acc:HGNC:53194]"}, {"versioned_ensembl_gene_id":"ENSG00000213587.3","gene_symbol":"AC126120.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50719482,"end":50719951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088538.12","gene_symbol":"DOCK3","gene_name":"dedicator of cytokinesis 3 [Source:HGNC Symbol;Acc:HGNC:2989]","synonyms":"PBP,MOCA,KIAA0299","biotype":"protein_coding","ncbi_id":"1795","summary":"This gene is specifically expressed in the central nervous system (CNS). It encodes a member of the DOCK (dedicator of cytokinesis) family of guanine nucleotide exchange factors (GEFs). This protein, dedicator of cytokinesis 3 (DOCK3), is also known as modifier of cell adhesion (MOCA) and presenilin-binding protein (PBP). The DOCK3 and DOCK1, -2 and -4 share several conserved amino acids in their DHR-2 (DOCK homology region 2) domains that are required for GEF activity, and bind directly to WAVE proteins [Wiskott-Aldrich syndrome protein (WASP) family Verprolin-homologous proteins] via their DHR-1 domains. The DOCK3 induces axonal outgrowth in CNS by stimulating membrane recruitment of the WAVE complex and activating the small G protein Rac1. This gene is associated with an attention deficit hyperactivity disorder-like phenotype by a complex chromosomal rearrangement. [provided by RefSeq, Aug 2010]","start":50675241,"end":51384198,"strand":1,"description":"dedicator of cytokinesis 3 [Source:HGNC Symbol;Acc:HGNC:2989]"}, {"versioned_ensembl_gene_id":"ENSG00000186510.11","gene_symbol":"CLCNKA","gene_name":"chloride voltage-gated channel Ka [Source:HGNC Symbol;Acc:HGNC:2026]","synonyms":"hClC-Ka","biotype":"protein_coding","ncbi_id":"1187","summary":"This gene is a member of the CLC family of voltage-gated chloride channels. The encoded protein is predicted to have 12 transmembrane domains, and requires a beta subunit called barttin to form a functional channel. It is thought to function in salt reabsorption in the kidney and potassium recycling in the inner ear. The gene is highly similar to CLCNKB, which is located 10 kb downstream from this gene. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":16018875,"end":16034050,"strand":1,"description":"chloride voltage-gated channel Ka [Source:HGNC Symbol;Acc:HGNC:2026]"}, {"versioned_ensembl_gene_id":"ENSG00000225176.2","gene_symbol":"ATP5LP4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130396","summary":null,"start":148703526,"end":148703832,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38165]"}, {"versioned_ensembl_gene_id":"ENSG00000204130.12","gene_symbol":"RUFY2","gene_name":"RUN and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19761]","synonyms":"RABIP4R,KIAA1537,FLJ10063,ZFYVE13","biotype":"protein_coding","ncbi_id":"55680","summary":null,"start":68341107,"end":68407294,"strand":-1,"description":"RUN and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19761]"}, {"versioned_ensembl_gene_id":"ENSG00000043591.5","gene_symbol":"ADRB1","gene_name":"adrenoceptor beta 1 [Source:HGNC Symbol;Acc:HGNC:285]","synonyms":"ADRB1R","biotype":"protein_coding","ncbi_id":"153","summary":"The adrenergic receptors (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide binding regulatory protein-coupled receptors that mediate the physiological effects of the hormone epinephrine and the neurotransmitter norepinephrine. Beta-1 adrenoceptors are predominately located in the heart. Specific polymorphisms in this gene have been shown to affect the resting heart rate and can be involved in heart failure. [provided by RefSeq, Sep 2019]","start":114044056,"end":114046908,"strand":1,"description":"adrenoceptor beta 1 [Source:HGNC Symbol;Acc:HGNC:285]"}, {"versioned_ensembl_gene_id":"ENSG00000251692.7","gene_symbol":"PTX4","gene_name":"pentraxin 4 [Source:HGNC Symbol;Acc:HGNC:14171]","synonyms":"C16orf38","biotype":"protein_coding","ncbi_id":"390667","summary":"This gene belongs to the pentraxin superfamily, whose members encode highly conserved multifunctional proteins. The encoded protein, like other members of this family, contains a conserved pentraxin domain at the C-terminus. The highest levels of expression of the protein were observed in bone marrow, small intestine and testes. [provided by RefSeq, Jun 2016]","start":1485886,"end":1488981,"strand":-1,"description":"pentraxin 4 [Source:HGNC Symbol;Acc:HGNC:14171]"}, {"versioned_ensembl_gene_id":"ENSG00000170417.15","gene_symbol":"TMEM182","gene_name":"transmembrane protein 182 [Source:HGNC Symbol;Acc:HGNC:26391]","synonyms":"FLJ30294","biotype":"protein_coding","ncbi_id":"130827","summary":null,"start":102736905,"end":103019900,"strand":1,"description":"transmembrane protein 182 [Source:HGNC Symbol;Acc:HGNC:26391]"}, {"versioned_ensembl_gene_id":"ENSG00000122696.13","gene_symbol":"SLC25A51","gene_name":"solute carrier family 25 member 51 [Source:HGNC Symbol;Acc:HGNC:23323]","synonyms":"MGC14836,MCART1,CG7943","biotype":"protein_coding","ncbi_id":"92014","summary":null,"start":37879400,"end":37904353,"strand":-1,"description":"solute carrier family 25 member 51 [Source:HGNC Symbol;Acc:HGNC:23323]"}, {"versioned_ensembl_gene_id":"ENSG00000078140.13","gene_symbol":"UBE2K","gene_name":"ubiquitin conjugating enzyme E2 K [Source:HGNC Symbol;Acc:HGNC:4914]","synonyms":"HIP2,UBC1,HYPG","biotype":"protein_coding","ncbi_id":"3093","summary":"The protein encoded by this gene belongs to the ubiquitin-conjugating enzyme family. This protein interacts with RING finger proteins, and it can ubiquitinate huntingtin, the gene product for Huntington's disease. Known functions for this protein include a role in aggregate formation of expanded polyglutamine proteins and the suppression of apoptosis in polyglutamine diseases, a role in the dislocation of newly synthesized MHC class I heavy chains from the endoplasmic reticulum, and involvement in foam cell formation. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":39698044,"end":39782792,"strand":1,"description":"ubiquitin conjugating enzyme E2 K [Source:HGNC Symbol;Acc:HGNC:4914]"}, {"versioned_ensembl_gene_id":"ENSG00000224966.4","gene_symbol":"TBC1D3P6","gene_name":"TBC1 domain family member 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43568]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101928566","summary":null,"start":15989871,"end":15994751,"strand":1,"description":"TBC1 domain family member 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43568]"}, {"versioned_ensembl_gene_id":"ENSG00000250329.1","gene_symbol":"KDELC1P1","gene_name":"KDEL motif containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39193]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100144494","summary":null,"start":128109486,"end":128110994,"strand":1,"description":"KDEL motif containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39193]"}, {"versioned_ensembl_gene_id":"ENSG00000271698.1","gene_symbol":"AC233992.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":144353228,"end":144355609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206187.3","gene_symbol":"LINC02346","gene_name":"long intergenic non-protein coding RNA 2346 [Source:HGNC Symbol;Acc:HGNC:53268]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128714","summary":null,"start":25902360,"end":26053120,"strand":1,"description":"long intergenic non-protein coding RNA 2346 [Source:HGNC Symbol;Acc:HGNC:53268]"}, {"versioned_ensembl_gene_id":"ENSG00000118513.18","gene_symbol":"MYB","gene_name":"MYB proto-oncogene, transcription factor [Source:HGNC Symbol;Acc:HGNC:7545]","synonyms":"c-myb","biotype":"protein_coding","ncbi_id":"4602","summary":"This gene encodes a protein with three HTH DNA-binding domains that functions as a transcription regulator. This protein plays an essential role in the regulation of hematopoiesis. This gene may be aberrently expressed or rearranged or undergo translocation in leukemias and lymphomas, and is considered to be an oncogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":135181315,"end":135219173,"strand":1,"description":"MYB proto-oncogene, transcription factor [Source:HGNC Symbol;Acc:HGNC:7545]"}, {"versioned_ensembl_gene_id":"ENSG00000170962.12","gene_symbol":"PDGFD","gene_name":"platelet derived growth factor D [Source:HGNC Symbol;Acc:HGNC:30620]","synonyms":"SCDGF-B,MSTP036,IEGF","biotype":"protein_coding","ncbi_id":"80310","summary":"The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a core motif of eight cysteines, seven of which are found in this factor. This gene product only forms homodimers and, therefore, does not dimerize with the other three family members. It differs from alpha and beta members of this family in having an unusual N-terminal domain, the CUB domain. Two splice variants have been identified for this gene. [provided by RefSeq, Jul 2008]","start":103907186,"end":104164379,"strand":-1,"description":"platelet derived growth factor D [Source:HGNC Symbol;Acc:HGNC:30620]"}, {"versioned_ensembl_gene_id":"ENSG00000170967.4","gene_symbol":"DDI1","gene_name":"DNA damage inducible 1 homolog 1 [Source:HGNC Symbol;Acc:HGNC:18961]","synonyms":"FLJ36017","biotype":"protein_coding","ncbi_id":"414301","summary":null,"start":104036580,"end":104039188,"strand":1,"description":"DNA damage inducible 1 homolog 1 [Source:HGNC Symbol;Acc:HGNC:18961]"}, {"versioned_ensembl_gene_id":"ENSG00000164924.17","gene_symbol":"YWHAZ","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta [Source:HGNC Symbol;Acc:HGNC:12855]","synonyms":"YWHAD,KCIP-1,14-3-3-zeta","biotype":"protein_coding","ncbi_id":"7534","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 99% identical to the mouse, rat and sheep orthologs. The encoded protein interacts with IRS1 protein, suggesting a role in regulating insulin sensitivity. Several transcript variants that differ in the 5' UTR but that encode the same protein have been identified for this gene. [provided by RefSeq, Oct 2008]","start":100916525,"end":100953388,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta [Source:HGNC Symbol;Acc:HGNC:12855]"}, {"versioned_ensembl_gene_id":"ENSG00000178146.9","gene_symbol":"AL672207.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101778969,"end":101780538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249752.1","gene_symbol":"AC108156.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149027445,"end":149062522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265337.1","gene_symbol":"AC079336.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32529008,"end":32530049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147155.10","gene_symbol":"EBP","gene_name":"emopamil binding protein (sterol isomerase) [Source:HGNC Symbol;Acc:HGNC:3133]","synonyms":"CPXD,CPX,CHO2,CDPX2","biotype":"protein_coding","ncbi_id":"10682","summary":"The protein encoded by this gene is an integral membrane protein of the endoplasmic reticulum. It is a high affinity binding protein for the antiischemic phenylalkylamine Ca2+ antagonist [3H]emopamil and the photoaffinity label [3H]azidopamil. It is similar to sigma receptors and may be a member of a superfamily of high affinity drug-binding proteins in the endoplasmic reticulum of different tissues. This protein shares structural features with bacterial and eukaryontic drug transporting proteins. It has four putative transmembrane segments and contains two conserved glutamate residues which may be involved in the transport of cationic amphiphilics. Another prominent feature of this protein is its high content of aromatic amino acid residues (>23%) in its transmembrane segments. These aromatic amino acid residues have been suggested to be involved in the drug transport by the P-glycoprotein. Mutations in this gene cause Chondrodysplasia punctata 2 (CDPX2; also known as Conradi-Hunermann syndrome). [provided by RefSeq, Jul 2008]","start":48521158,"end":48528716,"strand":1,"description":"emopamil binding protein (sterol isomerase) [Source:HGNC Symbol;Acc:HGNC:3133]"}, {"versioned_ensembl_gene_id":"ENSG00000266599.1","gene_symbol":"AC079336.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32518953,"end":32531492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280245.1","gene_symbol":"AC079336.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32504567,"end":32505644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227658.1","gene_symbol":"AC005160.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40775558,"end":40785217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069956.11","gene_symbol":"MAPK6","gene_name":"mitogen-activated protein kinase 6 [Source:HGNC Symbol;Acc:HGNC:6879]","synonyms":"PRKM6,p97MAPK,HsT17250,ERK3","biotype":"protein_coding","ncbi_id":"5597","summary":"The protein encoded by this gene is a member of the Ser/Thr protein kinase family, and is most closely related to mitogen-activated protein kinases (MAP kinases). MAP kinases also known as extracellular signal-regulated kinases (ERKs), are activated through protein phosphorylation cascades and act as integration points for multiple biochemical signals. This kinase is localized in the nucleus, and has been reported to be activated in fibroblasts upon treatment with serum or phorbol esters. [provided by RefSeq, Jul 2008]","start":51952106,"end":52067372,"strand":1,"description":"mitogen-activated protein kinase 6 [Source:HGNC Symbol;Acc:HGNC:6879]"}, {"versioned_ensembl_gene_id":"ENSG00000198933.9","gene_symbol":"TBKBP1","gene_name":"TBK1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:30140]","synonyms":"ProSAPiP2,KIAA0775","biotype":"protein_coding","ncbi_id":"9755","summary":"TBKBP1 is an adaptor protein that binds to TBK1 (MIM 604834) and is part of the interaction network in the TNF (MIM 191160)/NFKB (see MIM 164011) pathway (Bouwmeester et al., 2004 [PubMed 14743216]).[supplied by OMIM, Mar 2008]","start":47694081,"end":47712050,"strand":1,"description":"TBK1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:30140]"}, {"versioned_ensembl_gene_id":"ENSG00000080819.6","gene_symbol":"CPOX","gene_name":"coproporphyrinogen oxidase [Source:HGNC Symbol;Acc:HGNC:2321]","synonyms":"HCP,CPX,CPO","biotype":"protein_coding","ncbi_id":"1371","summary":"The protein encoded by this gene is the sixth enzyme of the heme biosynthetic pathway. The encoded enzyme is soluble and found in the intermembrane space of mitochondria. This enzyme catalyzes the stepwise oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX, a precursor of heme. Defects in this gene are a cause of hereditary coproporphyria (HCP).[provided by RefSeq, Oct 2009]","start":98521132,"end":98593723,"strand":-1,"description":"coproporphyrinogen oxidase [Source:HGNC Symbol;Acc:HGNC:2321]"}, {"versioned_ensembl_gene_id":"ENSG00000234907.1","gene_symbol":"AL593851.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132962511,"end":132962667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244538.1","gene_symbol":"AC098583.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22594196,"end":22594450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267383.6","gene_symbol":"AC011447.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20125377,"end":20321305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237638.1","gene_symbol":"LINC02245","gene_name":"long intergenic non-protein coding RNA 2245 [Source:HGNC Symbol;Acc:HGNC:53134]","synonyms":"lnc-SERTAD2-3","biotype":"lincRNA","ncbi_id":"400958","summary":null,"start":64901840,"end":64905137,"strand":-1,"description":"long intergenic non-protein coding RNA 2245 [Source:HGNC Symbol;Acc:HGNC:53134]"}, {"versioned_ensembl_gene_id":"ENSG00000143751.9","gene_symbol":"SDE2","gene_name":"SDE2 telomere maintenance homolog [Source:HGNC Symbol;Acc:HGNC:26643]","synonyms":"FLJ35382,C1orf55","biotype":"protein_coding","ncbi_id":"163859","summary":null,"start":225982702,"end":225999331,"strand":-1,"description":"SDE2 telomere maintenance homolog [Source:HGNC Symbol;Acc:HGNC:26643]"}, {"versioned_ensembl_gene_id":"ENSG00000129295.8","gene_symbol":"LRRC6","gene_name":"leucine rich repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:16725]","synonyms":"TSLRP,LRTP,CILD19","biotype":"protein_coding","ncbi_id":"23639","summary":"The protein encoded by this gene contains several leucine-rich repeat domains and appears to be involved in the motility of cilia. Defects in this gene are a cause of primary ciliary dyskinesia-19 (CILD19). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4, 11 and 22. [provided by RefSeq, Apr 2016]","start":132571953,"end":132675617,"strand":-1,"description":"leucine rich repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:16725]"}, {"versioned_ensembl_gene_id":"ENSG00000213708.6","gene_symbol":"SLC16A14P1","gene_name":"solute carrier family 16 member 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43809]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128685","summary":null,"start":106215763,"end":106217218,"strand":1,"description":"solute carrier family 16 member 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43809]"}, {"versioned_ensembl_gene_id":"ENSG00000205981.6","gene_symbol":"DNAJC19","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 [Source:HGNC Symbol;Acc:HGNC:30528]","synonyms":"TIMM14,Tim14,Pam18","biotype":"protein_coding","ncbi_id":"131118","summary":"The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19. [provided by RefSeq, Jan 2012]","start":180983709,"end":180989774,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 [Source:HGNC Symbol;Acc:HGNC:30528]"}, {"versioned_ensembl_gene_id":"ENSG00000254021.1","gene_symbol":"AC027031.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106265435,"end":106268741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274028.1","gene_symbol":"AC009237.16","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95588149,"end":95589253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241146.1","gene_symbol":"RPL7P41","gene_name":"ribosomal protein L7 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36297]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271222","summary":null,"start":52885429,"end":52886385,"strand":1,"description":"ribosomal protein L7 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36297]"}, {"versioned_ensembl_gene_id":"ENSG00000076650.6","gene_symbol":"GPATCH1","gene_name":"G-patch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24658]","synonyms":"GPATC1,FLJ38686,FLJ10206,ECGP","biotype":"protein_coding","ncbi_id":"55094","summary":null,"start":33080880,"end":33130542,"strand":1,"description":"G-patch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24658]"}, {"versioned_ensembl_gene_id":"ENSG00000206206.11","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"protein_coding","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33296480,"end":33307190,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000273669.1","gene_symbol":"AC015819.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75073543,"end":75074205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230083.1","gene_symbol":"AC009237.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95590969,"end":95591206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268070.1","gene_symbol":"AC006539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20033444,"end":20034332,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197124.11","gene_symbol":"ZNF682","gene_name":"zinc finger protein 682 [Source:HGNC Symbol;Acc:HGNC:28857]","synonyms":"BC39498_3","biotype":"protein_coding","ncbi_id":"91120","summary":null,"start":19997058,"end":20039506,"strand":-1,"description":"zinc finger protein 682 [Source:HGNC Symbol;Acc:HGNC:28857]"}, {"versioned_ensembl_gene_id":"ENSG00000048991.16","gene_symbol":"R3HDM1","gene_name":"R3H domain containing 1 [Source:HGNC Symbol;Acc:HGNC:9757]","synonyms":"R3HDM,KIAA0029","biotype":"protein_coding","ncbi_id":"23518","summary":null,"start":135531455,"end":135725270,"strand":1,"description":"R3H domain containing 1 [Source:HGNC Symbol;Acc:HGNC:9757]"}, {"versioned_ensembl_gene_id":"ENSG00000234709.2","gene_symbol":"UPF3AP3","gene_name":"UPF3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38395]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100422343","summary":null,"start":99998301,"end":99999069,"strand":-1,"description":"UPF3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38395]"}, {"versioned_ensembl_gene_id":"ENSG00000137563.11","gene_symbol":"GGH","gene_name":"gamma-glutamyl hydrolase [Source:HGNC Symbol;Acc:HGNC:4248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8836","summary":"This gene catalyzes the hydrolysis of folylpoly-gamma-glutamates and antifolylpoly-gamma-glutamates by the removal of gamma-linked polyglutamates and glutamate. [provided by RefSeq, Jul 2008]","start":63015079,"end":63039171,"strand":-1,"description":"gamma-glutamyl hydrolase [Source:HGNC Symbol;Acc:HGNC:4248]"}, {"versioned_ensembl_gene_id":"ENSG00000248261.1","gene_symbol":"AC008948.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102144077,"end":102146572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271429.1","gene_symbol":"RPL17P51","gene_name":"ribosomal protein L17 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:49100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480245","summary":null,"start":40224625,"end":40224862,"strand":-1,"description":"ribosomal protein L17 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:49100]"}, {"versioned_ensembl_gene_id":"ENSG00000126251.6","gene_symbol":"GPR42","gene_name":"G protein-coupled receptor 42 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4500]","synonyms":"GPR42P,GPR41L,FFAR3L","biotype":"protein_coding","ncbi_id":"2866","summary":null,"start":35370929,"end":35372962,"strand":1,"description":"G protein-coupled receptor 42 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4500]"}, {"versioned_ensembl_gene_id":"ENSG00000219375.1","gene_symbol":"AL139095.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7331286,"end":7331676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233694.5","gene_symbol":"AC007365.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64606975,"end":64616482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215483.10","gene_symbol":"LINC00598","gene_name":"long intergenic non-protein coding RNA 598 [Source:HGNC Symbol;Acc:HGNC:42770]","synonyms":"TTL","biotype":"lincRNA","ncbi_id":"646982","summary":null,"start":40079106,"end":40535807,"strand":-1,"description":"long intergenic non-protein coding RNA 598 [Source:HGNC Symbol;Acc:HGNC:42770]"}, {"versioned_ensembl_gene_id":"ENSG00000220920.1","gene_symbol":"AL023807.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17953572,"end":17953930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215630.6","gene_symbol":"GUSBP9","gene_name":"glucuronidase, beta pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42323]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100049076","summary":null,"start":71197646,"end":71208130,"strand":-1,"description":"glucuronidase, beta pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42323]"}, {"versioned_ensembl_gene_id":"ENSG00000077800.11","gene_symbol":"FKBP6","gene_name":"FK506 binding protein 6 [Source:HGNC Symbol;Acc:HGNC:3722]","synonyms":"PPIase,FKBP36","biotype":"protein_coding","ncbi_id":"8468","summary":"The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":73328164,"end":73358637,"strand":1,"description":"FK506 binding protein 6 [Source:HGNC Symbol;Acc:HGNC:3722]"}, {"versioned_ensembl_gene_id":"ENSG00000278911.1","gene_symbol":"AC015819.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75103587,"end":75106260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139714.12","gene_symbol":"MORN3","gene_name":"MORN repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:29807]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283385","summary":null,"start":121648742,"end":121672631,"strand":-1,"description":"MORN repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:29807]"}, {"versioned_ensembl_gene_id":"ENSG00000235558.3","gene_symbol":"AC146949.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71220356,"end":71259238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212932.3","gene_symbol":"RPL23AP4","gene_name":"ribosomal protein L23a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10321]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54029","summary":null,"start":46690764,"end":46691226,"strand":1,"description":"ribosomal protein L23a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10321]"}, {"versioned_ensembl_gene_id":"ENSG00000124783.12","gene_symbol":"SSR1","gene_name":"signal sequence receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:11323]","synonyms":"TRAPA","biotype":"protein_coding","ncbi_id":"6745","summary":"The signal sequence receptor (SSR) is a glycosylated endoplasmic reticulum (ER) membrane receptor associated with protein translocation across the ER membrane. The SSR consists of 2 subunits, a 34-kD glycoprotein encoded by this gene and a 22-kD glycoprotein. This gene generates several mRNA species as a result of complex alternative polyadenylation. This gene is unusual in that it utilizes arrays of polyA signal sequences that are mostly non-canonical. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":7268306,"end":7347446,"strand":-1,"description":"signal sequence receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:11323]"}, {"versioned_ensembl_gene_id":"ENSG00000272562.1","gene_symbol":"AL512343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":226060712,"end":226061876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163041.9","gene_symbol":"H3F3A","gene_name":"H3 histone family member 3A [Source:HGNC Symbol;Acc:HGNC:4764]","synonyms":"H3F3,H3.3A","biotype":"protein_coding","ncbi_id":"3020","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene contains introns and its mRNA is polyadenylated, unlike most histone genes. The protein encoded is a replication-independent member of the histone H3 family. [provided by RefSeq, Jul 2008]","start":226061851,"end":226072001,"strand":1,"description":"H3 histone family member 3A [Source:HGNC Symbol;Acc:HGNC:4764]"}, {"versioned_ensembl_gene_id":"ENSG00000231333.2","gene_symbol":"RPL34P6","gene_name":"ribosomal protein L34 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270998","summary":null,"start":200863808,"end":200864152,"strand":1,"description":"ribosomal protein L34 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35810]"}, {"versioned_ensembl_gene_id":"ENSG00000146857.3","gene_symbol":"STRA8","gene_name":"stimulated by retinoic acid 8 [Source:HGNC Symbol;Acc:HGNC:30653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"346673","summary":"This gene encodes a retinoic acid-responsive protein. A homologous protein in mouse has been shown to be involved in the regulation of meiotic initiation in both spermatogenesis and oogenesis, though feature differences between the mouse and human proteins suggest that these homologs are not entirely functionally equivalent. It is thought that this gene may play a role in spermatogenesis in humans. [provided by RefSeq, Nov 2010]","start":135231979,"end":135258492,"strand":1,"description":"stimulated by retinoic acid 8 [Source:HGNC Symbol;Acc:HGNC:30653]"}, {"versioned_ensembl_gene_id":"ENSG00000180011.6","gene_symbol":"ZADH2","gene_name":"zinc binding alcohol dehydrogenase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28697]","synonyms":"MGC45594","biotype":"protein_coding","ncbi_id":"284273","summary":null,"start":75195108,"end":75209348,"strand":-1,"description":"zinc binding alcohol dehydrogenase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28697]"}, {"versioned_ensembl_gene_id":"ENSG00000177558.3","gene_symbol":"FAM187B","gene_name":"family with sequence similarity 187 member B [Source:HGNC Symbol;Acc:HGNC:26366]","synonyms":"TMEM162,FLJ25660","biotype":"protein_coding","ncbi_id":"148109","summary":null,"start":35224800,"end":35228729,"strand":-1,"description":"family with sequence similarity 187 member B [Source:HGNC Symbol;Acc:HGNC:26366]"}, {"versioned_ensembl_gene_id":"ENSG00000170128.4","gene_symbol":"GPR25","gene_name":"G protein-coupled receptor 25 [Source:HGNC Symbol;Acc:HGNC:4480]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2848","summary":"This gene is intronless and encodes a member of the G-protein coupled receptor 1 family. G-protein coupled receptors are membrane proteins which activate signaling cascades as a response to extracellular stress. This gene has been linked to arterial stiffness. [provided by RefSeq, Nov 2012]","start":200872955,"end":200874178,"strand":1,"description":"G protein-coupled receptor 25 [Source:HGNC Symbol;Acc:HGNC:4480]"}, {"versioned_ensembl_gene_id":"ENSG00000167703.14","gene_symbol":"SLC43A2","gene_name":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]","synonyms":"MGC34680","biotype":"protein_coding","ncbi_id":"124935","summary":"This gene encodes a member of the L-amino acid transporter-3 or SLC43 family of transporters. The encoded protein mediates sodium-, chloride-, and pH-independent transport of L-isomers of neutral amino acids, including leucine, phenylalanine, valine and methionine. This protein may contribute to the transfer of amino acids across the placental membrane to the fetus. [provided by RefSeq, Mar 2016]","start":1569267,"end":1628886,"strand":-1,"description":"solute carrier family 43 member 2 [Source:HGNC Symbol;Acc:HGNC:23087]"}, {"versioned_ensembl_gene_id":"ENSG00000165702.13","gene_symbol":"GFI1B","gene_name":"growth factor independent 1B transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:4238]","synonyms":"ZNF163B","biotype":"protein_coding","ncbi_id":"8328","summary":"This gene encodes a zinc-finger containing transcriptional regulator that is primarily expressed in cells of hematopoietic lineage. The encoded protein complexes with numerous other transcriptional regulatory proteins including GATA-1, runt-related transcription factor 1 and histone deacetylases to control expression of genes involved in the development and maturation of erythrocytes and megakaryocytes. Mutations in this gene are the cause of the autosomal dominant platelet disorder, platelet-type bleeding disorder-17. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":132944000,"end":132991687,"strand":1,"description":"growth factor independent 1B transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:4238]"}, {"versioned_ensembl_gene_id":"ENSG00000276067.2","gene_symbol":"AC009542.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135246113,"end":135317752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265921.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31075504,"end":31075603,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200612.1","gene_symbol":"SNORD114-25","gene_name":"small nucleolar RNA, C/D box 114-25 [Source:HGNC Symbol;Acc:HGNC:33013]","synonyms":"14q(II-25)","biotype":"snoRNA","ncbi_id":"767605","summary":null,"start":100986057,"end":100986128,"strand":1,"description":"small nucleolar RNA, C/D box 114-25 [Source:HGNC Symbol;Acc:HGNC:33013]"}, {"versioned_ensembl_gene_id":"ENSG00000244376.3","gene_symbol":"RN7SL636P","gene_name":"RNA, 7SL, cytoplasmic 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:46652]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481097","summary":null,"start":50429190,"end":50429483,"strand":-1,"description":"RNA, 7SL, cytoplasmic 636, pseudogene [Source:HGNC Symbol;Acc:HGNC:46652]"}, {"versioned_ensembl_gene_id":"ENSG00000201939.1","gene_symbol":"RNA5SP224","gene_name":"RNA, 5S ribosomal pseudogene 224 [Source:HGNC Symbol;Acc:HGNC:43124]","synonyms":"RN5S224","biotype":"rRNA","ncbi_id":"100873483","summary":null,"start":153159220,"end":153159345,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 224 [Source:HGNC Symbol;Acc:HGNC:43124]"}, {"versioned_ensembl_gene_id":"ENSG00000284410.1","gene_symbol":"MIR6733","gene_name":"microRNA 6733 [Source:HGNC Symbol;Acc:HGNC:50239]","synonyms":"hsa-mir-6733","biotype":"miRNA","ncbi_id":"102465439","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43171652,"end":43171712,"strand":-1,"description":"microRNA 6733 [Source:HGNC Symbol;Acc:HGNC:50239]"}, {"versioned_ensembl_gene_id":"ENSG00000223318.1","gene_symbol":"RNA5SP111","gene_name":"RNA, 5S ribosomal pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:42909]","synonyms":"RN5S111","biotype":"rRNA","ncbi_id":"100873381","summary":null,"start":164895677,"end":164895777,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 111 [Source:HGNC Symbol;Acc:HGNC:42909]"}, {"versioned_ensembl_gene_id":"ENSG00000271818.1","gene_symbol":"RN7SKP4","gene_name":"RNA, 7SK small nuclear pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42622]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873848","summary":null,"start":45123093,"end":45123414,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42622]"}, {"versioned_ensembl_gene_id":"ENSG00000252469.1","gene_symbol":"RNU7-160P","gene_name":"RNA, U7 small nuclear 160 pseudogene [Source:HGNC Symbol;Acc:HGNC:45694]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479085","summary":null,"start":103550345,"end":103550406,"strand":1,"description":"RNA, U7 small nuclear 160 pseudogene [Source:HGNC Symbol;Acc:HGNC:45694]"}, {"versioned_ensembl_gene_id":"ENSG00000207061.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":156186122,"end":156186223,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275384.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000252473.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"U67,RNU67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":39283657,"end":39283791,"strand":-1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000277610.1","gene_symbol":"RNVU1-4","gene_name":"RNA, variant U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:48312]","synonyms":"vU1.5,vU1.4,RNVU1-5,RNU1-50,RNU1-102","biotype":"snRNA","ncbi_id":"101954264","summary":null,"start":120942600,"end":120942763,"strand":1,"description":"RNA, variant U1 small nuclear 4 [Source:HGNC Symbol;Acc:HGNC:48312]"}, {"versioned_ensembl_gene_id":"ENSG00000276767.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28535771,"end":28536060,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000242764.3","gene_symbol":"RN7SL824P","gene_name":"RNA, 7SL, cytoplasmic 824, pseudogene [Source:HGNC Symbol;Acc:HGNC:46840]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481146","summary":null,"start":92402389,"end":92402685,"strand":-1,"description":"RNA, 7SL, cytoplasmic 824, pseudogene [Source:HGNC Symbol;Acc:HGNC:46840]"}, {"versioned_ensembl_gene_id":"ENSG00000201027.1","gene_symbol":"RN7SKP107","gene_name":"RNA, 7SK small nuclear pseudogene 107 [Source:HGNC Symbol;Acc:HGNC:45831]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480464","summary":null,"start":89621918,"end":89622207,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 107 [Source:HGNC Symbol;Acc:HGNC:45831]"}, {"versioned_ensembl_gene_id":"ENSG00000283432.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":135315418,"end":135315522,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000274505.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11753666,"end":11753948,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284107.1","gene_symbol":"MIR19B2","gene_name":"microRNA 19b-2 [Source:HGNC Symbol;Acc:HGNC:31576]","synonyms":"MIRN19B2,hsa-mir-19b-2","biotype":"miRNA","ncbi_id":"406981","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134169671,"end":134169766,"strand":-1,"description":"microRNA 19b-2 [Source:HGNC Symbol;Acc:HGNC:31576]"}, {"versioned_ensembl_gene_id":"ENSG00000207139.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":197685640,"end":197685740,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200522.1","gene_symbol":"RNU6-957P","gene_name":"RNA, U6 small nuclear 957, pseudogene [Source:HGNC Symbol;Acc:HGNC:47920]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479989","summary":null,"start":110722250,"end":110722348,"strand":-1,"description":"RNA, U6 small nuclear 957, pseudogene [Source:HGNC Symbol;Acc:HGNC:47920]"}, {"versioned_ensembl_gene_id":"ENSG00000206705.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136129980,"end":136130081,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238793.1","gene_symbol":"SNORD124","gene_name":"small nucleolar RNA, C/D box 124 [Source:HGNC Symbol;Acc:HGNC:33563]","synonyms":null,"biotype":"snoRNA","ncbi_id":"101340251","summary":null,"start":40027542,"end":40027645,"strand":-1,"description":"small nucleolar RNA, C/D box 124 [Source:HGNC Symbol;Acc:HGNC:33563]"}, {"versioned_ensembl_gene_id":"ENSG00000239577.3","gene_symbol":"RN7SL388P","gene_name":"RNA, 7SL, cytoplasmic 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:46404]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479365","summary":null,"start":72198712,"end":72199050,"strand":1,"description":"RNA, 7SL, cytoplasmic 388, pseudogene [Source:HGNC Symbol;Acc:HGNC:46404]"}, {"versioned_ensembl_gene_id":"ENSG00000251718.1","gene_symbol":"RNU2-13P","gene_name":"RNA, U2 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:48506]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480203","summary":null,"start":11561194,"end":11561306,"strand":1,"description":"RNA, U2 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:48506]"}, {"versioned_ensembl_gene_id":"ENSG00000201801.1","gene_symbol":"RNU5E-4P","gene_name":"RNA, U5E small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42513]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873829","summary":null,"start":11909808,"end":11909927,"strand":-1,"description":"RNA, U5E small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42513]"}, {"versioned_ensembl_gene_id":"ENSG00000252982.1","gene_symbol":"RN7SKP234","gene_name":"RNA, 7SK small nuclear pseudogene 234 [Source:HGNC Symbol;Acc:HGNC:45958]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480368","summary":null,"start":174057641,"end":174057864,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 234 [Source:HGNC Symbol;Acc:HGNC:45958]"}, {"versioned_ensembl_gene_id":"ENSG00000222282.1","gene_symbol":"RNU6-584P","gene_name":"RNA, U6 small nuclear 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:47547]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479825","summary":null,"start":37885023,"end":37885117,"strand":1,"description":"RNA, U6 small nuclear 584, pseudogene [Source:HGNC Symbol;Acc:HGNC:47547]"}, {"versioned_ensembl_gene_id":"ENSG00000265986.1","gene_symbol":"MIR4735","gene_name":"microRNA 4735 [Source:HGNC Symbol;Acc:HGNC:41888]","synonyms":"hsa-mir-4735","biotype":"miRNA","ncbi_id":"100616363","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":196582413,"end":196582481,"strand":-1,"description":"microRNA 4735 [Source:HGNC Symbol;Acc:HGNC:41888]"}, {"versioned_ensembl_gene_id":"ENSG00000284271.1","gene_symbol":"AL158844.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":112956601,"end":112956752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280908.2","gene_symbol":"PADI4","gene_name":"peptidyl arginine deiminase 4 [Source:HGNC Symbol;Acc:HGNC:18368]","synonyms":"PAD,PDI5,PDI4,PADI5","biotype":"protein_coding","ncbi_id":"23569","summary":"This gene is a member of a gene family which encodes enzymes responsible for the conversion of arginine residues to citrulline residues. This gene may play a role in granulocyte and macrophage development leading to inflammation and immune response. [provided by RefSeq, Jul 2008]","start":17310905,"end":17366713,"strand":1,"description":"peptidyl arginine deiminase 4 [Source:HGNC Symbol;Acc:HGNC:18368]"}, {"versioned_ensembl_gene_id":"ENSG00000208883.1","gene_symbol":"SNORD96B","gene_name":"small nucleolar RNA, C/D box 96B [Source:HGNC Symbol;Acc:HGNC:32759]","synonyms":"U96b","biotype":"snoRNA","ncbi_id":"692226","summary":null,"start":110224985,"end":110225063,"strand":-1,"description":"small nucleolar RNA, C/D box 96B [Source:HGNC Symbol;Acc:HGNC:32759]"}, {"versioned_ensembl_gene_id":"ENSG00000283612.1","gene_symbol":"MIR103B1","gene_name":"microRNA 103b-1 [Source:HGNC Symbol;Acc:HGNC:35384]","synonyms":"MIRN103-1AS,MIR103-1AS,hsa-mir-103b-1,hsa-mir-103-1-as","biotype":"miRNA","ncbi_id":"100302238","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168560904,"end":168560965,"strand":1,"description":"microRNA 103b-1 [Source:HGNC Symbol;Acc:HGNC:35384]"}, {"versioned_ensembl_gene_id":"ENSG00000264390.1","gene_symbol":"MIR4465","gene_name":"microRNA 4465 [Source:HGNC Symbol;Acc:HGNC:41842]","synonyms":"hsa-mir-4465","biotype":"miRNA","ncbi_id":"100616180","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140683814,"end":140683883,"strand":1,"description":"microRNA 4465 [Source:HGNC Symbol;Acc:HGNC:41842]"}, {"versioned_ensembl_gene_id":"ENSG00000252534.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":60748940,"end":60749046,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207980.1","gene_symbol":"MIR23A","gene_name":"microRNA 23a [Source:HGNC Symbol;Acc:HGNC:31605]","synonyms":"MIRN23A,hsa-mir-23a","biotype":"miRNA","ncbi_id":"407010","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13836587,"end":13836659,"strand":-1,"description":"microRNA 23a [Source:HGNC Symbol;Acc:HGNC:31605]"}, {"versioned_ensembl_gene_id":"ENSG00000278322.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000202281.1","gene_symbol":"RNA5SP235","gene_name":"RNA, 5S ribosomal pseudogene 235 [Source:HGNC Symbol;Acc:HGNC:43135]","synonyms":"RN5S235","biotype":"rRNA","ncbi_id":"100873493","summary":null,"start":83017898,"end":83018011,"strand":1,"description":"RNA, 5S ribosomal pseudogene 235 [Source:HGNC Symbol;Acc:HGNC:43135]"}, {"versioned_ensembl_gene_id":"ENSG00000265538.1","gene_symbol":"MIR4421","gene_name":"microRNA 4421 [Source:HGNC Symbol;Acc:HGNC:41879]","synonyms":"hsa-mir-4421","biotype":"miRNA","ncbi_id":"100616189","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51059837,"end":51059905,"strand":1,"description":"microRNA 4421 [Source:HGNC Symbol;Acc:HGNC:41879]"}, {"versioned_ensembl_gene_id":"ENSG00000265607.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31528550,"end":31528627,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000222845.1","gene_symbol":"RN7SKP42","gene_name":"RNA, 7SK small nuclear pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:45766]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480846","summary":null,"start":187122562,"end":187122861,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:45766]"}, {"versioned_ensembl_gene_id":"ENSG00000274998.1","gene_symbol":"SNORA17A","gene_name":"small nucleolar RNA, H/ACA box 17A [Source:HGNC Symbol;Acc:HGNC:32607]","synonyms":"SNORA17,ACA17","biotype":"snoRNA","ncbi_id":"677804","summary":null,"start":136726747,"end":136726879,"strand":-1,"description":"small nucleolar RNA, H/ACA box 17A [Source:HGNC Symbol;Acc:HGNC:32607]"}, {"versioned_ensembl_gene_id":"ENSG00000265732.1","gene_symbol":"SNORD48","gene_name":"small nucleolar RNA, C/D box 48 [Source:HGNC Symbol;Acc:HGNC:10188]","synonyms":"U48,RNU48,U48,RNU48","biotype":"snoRNA","ncbi_id":"26801","summary":null,"start":31825510,"end":31825572,"strand":1,"description":"small nucleolar RNA, C/D box 48 [Source:HGNC Symbol;Acc:HGNC:10188]"}, {"versioned_ensembl_gene_id":"ENSG00000201671.1","gene_symbol":"RNA5SP90","gene_name":"RNA, 5S ribosomal pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:42888]","synonyms":"RN5S90","biotype":"rRNA","ncbi_id":"100873323","summary":null,"start":31228312,"end":31228410,"strand":1,"description":"RNA, 5S ribosomal pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:42888]"}, {"versioned_ensembl_gene_id":"ENSG00000212605.1","gene_symbol":"RNU1-56P","gene_name":"RNA, U1 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48398]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480165","summary":null,"start":71020275,"end":71020438,"strand":-1,"description":"RNA, U1 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:48398]"}, {"versioned_ensembl_gene_id":"ENSG00000202255.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36668559,"end":36668670,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207046.1","gene_symbol":"RNU6-886P","gene_name":"RNA, U6 small nuclear 886, pseudogene [Source:HGNC Symbol;Acc:HGNC:47849]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479958","summary":null,"start":37434469,"end":37434573,"strand":-1,"description":"RNA, U6 small nuclear 886, pseudogene [Source:HGNC Symbol;Acc:HGNC:47849]"}, {"versioned_ensembl_gene_id":"ENSG00000212191.1","gene_symbol":"SNORD65","gene_name":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]","synonyms":"SNORD65A,HBII-135","biotype":"snoRNA","ncbi_id":"692106","summary":null,"start":178685886,"end":178685956,"strand":-1,"description":"Small nucleolar RNA SNORD65 [Source:RFAM;Acc:RF00571]"}, {"versioned_ensembl_gene_id":"ENSG00000202374.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"RNU108,E2,RNE2,E2-1","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":67747236,"end":67747386,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000263785.1","gene_symbol":"MIR3182","gene_name":"microRNA 3182 [Source:HGNC Symbol;Acc:HGNC:38317]","synonyms":"hsa-mir-3182","biotype":"miRNA","ncbi_id":"100422853","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":83508346,"end":83508408,"strand":1,"description":"microRNA 3182 [Source:HGNC Symbol;Acc:HGNC:38317]"}, {"versioned_ensembl_gene_id":"ENSG00000207589.1","gene_symbol":"MIR508","gene_name":"microRNA 508 [Source:HGNC Symbol;Acc:HGNC:32145]","synonyms":"MIRN508,hsa-mir-508","biotype":"miRNA","ncbi_id":"574513","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147236913,"end":147237027,"strand":-1,"description":"microRNA 508 [Source:HGNC Symbol;Acc:HGNC:32145]"}, {"versioned_ensembl_gene_id":"ENSG00000207492.1","gene_symbol":"RNU6-713P","gene_name":"RNA, U6 small nuclear 713, pseudogene [Source:HGNC Symbol;Acc:HGNC:47676]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479882","summary":null,"start":40554161,"end":40554267,"strand":-1,"description":"RNA, U6 small nuclear 713, pseudogene [Source:HGNC Symbol;Acc:HGNC:47676]"}, {"versioned_ensembl_gene_id":"ENSG00000209042.1","gene_symbol":"SNORD12C","gene_name":"small nucleolar RNA, C/D box 12C [Source:HGNC Symbol;Acc:HGNC:10105]","synonyms":"U106,SNORD106,RNU106","biotype":"snoRNA","ncbi_id":"26765","summary":null,"start":49278940,"end":49279028,"strand":1,"description":"small nucleolar RNA, C/D box 12C [Source:HGNC Symbol;Acc:HGNC:10105]"}, {"versioned_ensembl_gene_id":"ENSG00000240533.3","gene_symbol":"RN7SL69P","gene_name":"RNA, 7SL, cytoplasmic 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:46085]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480940","summary":null,"start":6095699,"end":6095970,"strand":-1,"description":"RNA, 7SL, cytoplasmic 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:46085]"}, {"versioned_ensembl_gene_id":"ENSG00000278222.1","gene_symbol":"RN7SL536P","gene_name":"RNA, 7SL, cytoplasmic 536, pseudogene [Source:HGNC Symbol;Acc:HGNC:46552]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481068","summary":null,"start":23363272,"end":23363561,"strand":1,"description":"RNA, 7SL, cytoplasmic 536, pseudogene [Source:HGNC Symbol;Acc:HGNC:46552]"}, {"versioned_ensembl_gene_id":"ENSG00000212498.1","gene_symbol":"SNORD86","gene_name":"small nucleolar RNA, C/D box 86 [Source:HGNC Symbol;Acc:HGNC:32745]","synonyms":"U86","biotype":"snoRNA","ncbi_id":"692201","summary":null,"start":2656097,"end":2656182,"strand":1,"description":"small nucleolar RNA, C/D box 86 [Source:HGNC Symbol;Acc:HGNC:32745]"}, {"versioned_ensembl_gene_id":"ENSG00000273728.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1105307,"end":1105573,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000264933.2","gene_symbol":"RN7SL190P","gene_name":"RNA, 7SL, cytoplasmic 190, pseudogene [Source:HGNC Symbol;Acc:HGNC:46206]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479291","summary":null,"start":123811331,"end":123811587,"strand":-1,"description":"RNA, 7SL, cytoplasmic 190, pseudogene [Source:HGNC Symbol;Acc:HGNC:46206]"}, {"versioned_ensembl_gene_id":"ENSG00000252625.1","gene_symbol":"RNU1-40P","gene_name":"RNA, U1 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:48382]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480158","summary":null,"start":25928979,"end":25929142,"strand":1,"description":"RNA, U1 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:48382]"}, {"versioned_ensembl_gene_id":"ENSG00000278724.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":151275509,"end":151275789,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276353.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":54130582,"end":54130860,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212590.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":152609313,"end":152609434,"strand":1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000221459.1","gene_symbol":"SNORA11C","gene_name":"small nucleolar RNA, H/ACA box 11C [Source:HGNC Symbol;Acc:HGNC:33621]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124540","summary":null,"start":47388649,"end":47388777,"strand":1,"description":"small nucleolar RNA, H/ACA box 11C [Source:HGNC Symbol;Acc:HGNC:33621]"}, {"versioned_ensembl_gene_id":"ENSG00000251324.1","gene_symbol":"LINC01386","gene_name":"long intergenic non-protein coding RNA 1386 [Source:HGNC Symbol;Acc:HGNC:50659]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355294","summary":null,"start":73454187,"end":73472896,"strand":-1,"description":"long intergenic non-protein coding RNA 1386 [Source:HGNC Symbol;Acc:HGNC:50659]"}, {"versioned_ensembl_gene_id":"ENSG00000263154.1","gene_symbol":"AC110285.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81362272,"end":81374214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275966.1","gene_symbol":"AC110285.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81345476,"end":81345966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221238.1","gene_symbol":"MIR1285-2","gene_name":"microRNA 1285-2 [Source:HGNC Symbol;Acc:HGNC:35278]","synonyms":"MIRN1285-2,hsa-mir-1285-2","biotype":"miRNA","ncbi_id":"100302268","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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{"versioned_ensembl_gene_id":"ENSG00000244335.3","gene_symbol":"RN7SL687P","gene_name":"RNA, 7SL, cytoplasmic 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:46703]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481110","summary":null,"start":153666226,"end":153666510,"strand":1,"description":"RNA, 7SL, cytoplasmic 687, pseudogene [Source:HGNC Symbol;Acc:HGNC:46703]"}, {"versioned_ensembl_gene_id":"ENSG00000243267.3","gene_symbol":"RN7SL614P","gene_name":"RNA, 7SL, cytoplasmic 614, pseudogene [Source:HGNC Symbol;Acc:HGNC:46630]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481089","summary":null,"start":10616836,"end":10617115,"strand":1,"description":"RNA, 7SL, cytoplasmic 614, pseudogene [Source:HGNC Symbol;Acc:HGNC:46630]"}, {"versioned_ensembl_gene_id":"ENSG00000206672.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67625356,"end":67625464,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251783.1","gene_symbol":"RNU6-1170P","gene_name":"RNA, U6 small nuclear 1170, pseudogene [Source:HGNC Symbol;Acc:HGNC:48133]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480081","summary":null,"start":42605158,"end":42605263,"strand":1,"description":"RNA, U6 small nuclear 1170, pseudogene [Source:HGNC Symbol;Acc:HGNC:48133]"}, {"versioned_ensembl_gene_id":"ENSG00000201184.1","gene_symbol":"RNU4-68P","gene_name":"RNA, U4 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:47004]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479589","summary":null,"start":103567405,"end":103567545,"strand":1,"description":"RNA, U4 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:47004]"}, {"versioned_ensembl_gene_id":"ENSG00000274025.1","gene_symbol":"MIR3670-4","gene_name":"microRNA 3670-4 [Source:HGNC Symbol;Acc:HGNC:50828]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504740","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18488301,"end":18488365,"strand":-1,"description":"microRNA 3670-4 [Source:HGNC Symbol;Acc:HGNC:50828]"}, {"versioned_ensembl_gene_id":"ENSG00000195024.2","gene_symbol":"RNU1-15P","gene_name":"RNA, U1 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:10140]","synonyms":"U1P11,RNU1P8","biotype":"snRNA","ncbi_id":"26858","summary":null,"start":21381363,"end":21381506,"strand":1,"description":"RNA, U1 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:10140]"}, {"versioned_ensembl_gene_id":"ENSG00000206976.1","gene_symbol":"SNORA7","gene_name":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":3922567,"end":3922703,"strand":1,"description":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]"}, {"versioned_ensembl_gene_id":"ENSG00000252366.1","gene_symbol":"RNA5SP367","gene_name":"RNA, 5S ribosomal pseudogene 367 [Source:HGNC 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Symbol;Acc:HGNC:47281]"}, {"versioned_ensembl_gene_id":"ENSG00000201689.1","gene_symbol":"SNORD114-29","gene_name":"small nucleolar RNA, C/D box 114-29 [Source:HGNC Symbol;Acc:HGNC:33017]","synonyms":"14q(II-29)","biotype":"snoRNA","ncbi_id":"767610","summary":null,"start":100990091,"end":100990160,"strand":1,"description":"small nucleolar RNA, C/D box 114-29 [Source:HGNC Symbol;Acc:HGNC:33017]"}, {"versioned_ensembl_gene_id":"ENSG00000207342.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88840165,"end":88840263,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251987.1","gene_symbol":"SNORD63","gene_name":"Small nucleolar RNA SNORD63 [Source:RFAM;Acc:RF00154]","synonyms":"U63,SNORD63A,RNU63","biotype":"snoRNA","ncbi_id":"26785","summary":null,"start":53530322,"end":53530401,"strand":-1,"description":"Small nucleolar RNA SNORD63 [Source:RFAM;Acc:RF00154]"}, {"versioned_ensembl_gene_id":"ENSG00000222500.1","gene_symbol":"RNA5SP475","gene_name":"RNA, 5S ribosomal pseudogene 475 [Source:HGNC Symbol;Acc:HGNC:43375]","synonyms":"RN5S475","biotype":"rRNA","ncbi_id":"100873717","summary":null,"start":15280764,"end":15280873,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 475 [Source:HGNC Symbol;Acc:HGNC:43375]"}, {"versioned_ensembl_gene_id":"ENSG00000238632.1","gene_symbol":"RNU7-126P","gene_name":"RNA, U7 small nuclear 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:45660]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479073","summary":null,"start":25598564,"end":25598625,"strand":-1,"description":"RNA, U7 small nuclear 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:45660]"}, {"versioned_ensembl_gene_id":"ENSG00000265641.1","gene_symbol":"MIR3929","gene_name":"microRNA 3929 [Source:HGNC Symbol;Acc:HGNC:38945]","synonyms":"hsa-mir-3929","biotype":"miRNA","ncbi_id":"100500864","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35934088,"end":35934142,"strand":-1,"description":"microRNA 3929 [Source:HGNC Symbol;Acc:HGNC:38945]"}, {"versioned_ensembl_gene_id":"ENSG00000199241.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":240698320,"end":240698429,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223225.1","gene_symbol":"RNU6-1054P","gene_name":"RNA, U6 small nuclear 1054, pseudogene [Source:HGNC Symbol;Acc:HGNC:48017]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480029","summary":null,"start":118606450,"end":118606553,"strand":1,"description":"RNA, U6 small nuclear 1054, pseudogene [Source:HGNC Symbol;Acc:HGNC:48017]"}, {"versioned_ensembl_gene_id":"ENSG00000283645.1","gene_symbol":"MIR5583-2","gene_name":"microRNA 5583-2 [Source:HGNC Symbol;Acc:HGNC:43471]","synonyms":"hsa-mir-5583-2","biotype":"miRNA","ncbi_id":"100846997","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39676719,"end":39676777,"strand":-1,"description":"microRNA 5583-2 [Source:HGNC Symbol;Acc:HGNC:43471]"}, {"versioned_ensembl_gene_id":"ENSG00000277916.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29171285,"end":29171453,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000199392.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":77431563,"end":77431689,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000274309.1","gene_symbol":"SNORA71E","gene_name":"small nucleolar RNA, H/ACA box 71E [Source:HGNC Symbol;Acc:HGNC:32632]","synonyms":"SNORA39,ACA39","biotype":"snoRNA","ncbi_id":"677821","summary":null,"start":38448084,"end":38448215,"strand":1,"description":"small nucleolar RNA, H/ACA box 71E [Source:HGNC Symbol;Acc:HGNC:32632]"}, {"versioned_ensembl_gene_id":"ENSG00000207711.1","gene_symbol":"MIR525","gene_name":"microRNA 525 [Source:HGNC Symbol;Acc:HGNC:32102]","synonyms":"MIRN525,hsa-mir-525","biotype":"miRNA","ncbi_id":"574470","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53697533,"end":53697617,"strand":1,"description":"microRNA 525 [Source:HGNC Symbol;Acc:HGNC:32102]"}, {"versioned_ensembl_gene_id":"ENSG00000199122.3","gene_symbol":"MIR148B","gene_name":"microRNA 148b [Source:HGNC Symbol;Acc:HGNC:31761]","synonyms":"MIRN148B,hsa-mir-148b","biotype":"miRNA","ncbi_id":"442892","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54337216,"end":54337314,"strand":1,"description":"microRNA 148b [Source:HGNC Symbol;Acc:HGNC:31761]"}, {"versioned_ensembl_gene_id":"ENSG00000199636.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":24429505,"end":24429609,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207971.1","gene_symbol":"MIR125B1","gene_name":"microRNA 125b-1 [Source:HGNC Symbol;Acc:HGNC:31506]","synonyms":"MIRN125B1,hsa-mir-125b-1","biotype":"miRNA","ncbi_id":"406911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122099757,"end":122099844,"strand":-1,"description":"microRNA 125b-1 [Source:HGNC Symbol;Acc:HGNC:31506]"}, {"versioned_ensembl_gene_id":"ENSG00000201892.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140992543,"end":140992659,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000180340.6","gene_symbol":"FZD2","gene_name":"frizzled class receptor 2 [Source:HGNC Symbol;Acc:HGNC:4040]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2535","summary":"This intronless gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the wingless type MMTV integration site family of signaling proteins. This gene encodes a protein that is coupled to the beta-catenin canonical signaling pathway. Competition between the wingless-type MMTV integration site family, member 3A and wingless-type MMTV integration site family, member 5A gene products for binding of this protein is thought to regulate the beta-catenin-dependent and -independent pathways. [provided by RefSeq, Dec 2010]","start":44557459,"end":44559570,"strand":1,"description":"frizzled class receptor 2 [Source:HGNC Symbol;Acc:HGNC:4040]"}, {"versioned_ensembl_gene_id":"ENSG00000210741.1","gene_symbol":"MIR196A1","gene_name":"microRNA 196a-1 [Source:HGNC Symbol;Acc:HGNC:31567]","synonyms":"MIRN196A1,MIRN196-1,hsa-mir-196a-1,hsa-mir-196-1","biotype":"miRNA","ncbi_id":"406972","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48632490,"end":48632559,"strand":-1,"description":"microRNA 196a-1 [Source:HGNC Symbol;Acc:HGNC:31567]"}, {"versioned_ensembl_gene_id":"ENSG00000200313.1","gene_symbol":"RNA5-8SP7","gene_name":"RNA, 5.8S ribosomal pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:41962]","synonyms":"RN5-8S7","biotype":"rRNA","ncbi_id":"100873573","summary":null,"start":5346006,"end":5346160,"strand":-1,"description":"RNA, 5.8S ribosomal pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:41962]"}, {"versioned_ensembl_gene_id":"ENSG00000265673.1","gene_symbol":"MIR4508","gene_name":"microRNA 4508 [Source:HGNC Symbol;Acc:HGNC:41659]","synonyms":"hsa-mir-4508","biotype":"miRNA","ncbi_id":"100616275","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23562062,"end":23562131,"strand":-1,"description":"microRNA 4508 [Source:HGNC Symbol;Acc:HGNC:41659]"}, {"versioned_ensembl_gene_id":"ENSG00000277524.1","gene_symbol":"SMAD5-AS1_3","gene_name":"SMAD5 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02175]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136133912,"end":136134035,"strand":1,"description":"SMAD5 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02175]"}, {"versioned_ensembl_gene_id":"ENSG00000200752.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50959267,"end":50959379,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206918.1","gene_symbol":"RNU6-1181P","gene_name":"RNA, U6 small nuclear 1181, pseudogene [Source:HGNC Symbol;Acc:HGNC:48144]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480085","summary":null,"start":57512450,"end":57512555,"strand":1,"description":"RNA, U6 small nuclear 1181, pseudogene [Source:HGNC Symbol;Acc:HGNC:48144]"}, {"versioned_ensembl_gene_id":"ENSG00000222436.1","gene_symbol":"RN7SKP278","gene_name":"RNA, 7SK small nuclear pseudogene 278 [Source:HGNC Symbol;Acc:HGNC:46002]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480918","summary":null,"start":108940969,"end":108941310,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 278 [Source:HGNC Symbol;Acc:HGNC:46002]"}, {"versioned_ensembl_gene_id":"ENSG00000212138.1","gene_symbol":"RNA5SP372","gene_name":"RNA, 5S ribosomal pseudogene 372 [Source:HGNC Symbol;Acc:HGNC:43272]","synonyms":"RN5S372","biotype":"rRNA","ncbi_id":"100873630","summary":null,"start":109059986,"end":109060100,"strand":1,"description":"RNA, 5S ribosomal pseudogene 372 [Source:HGNC Symbol;Acc:HGNC:43272]"}, {"versioned_ensembl_gene_id":"ENSG00000200421.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37737955,"end":37738054,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252289.1","gene_symbol":"RNA5SP519","gene_name":"RNA, 5S ribosomal pseudogene 519 [Source:HGNC Symbol;Acc:HGNC:43419]","synonyms":"RN5S519","biotype":"rRNA","ncbi_id":"100873570","summary":null,"start":10092875,"end":10092993,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 519 [Source:HGNC Symbol;Acc:HGNC:43419]"}, {"versioned_ensembl_gene_id":"ENSG00000222821.1","gene_symbol":"RNU4-27P","gene_name":"RNA, U4 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46963]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481180","summary":null,"start":36402721,"end":36402859,"strand":-1,"description":"RNA, U4 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:46963]"}, {"versioned_ensembl_gene_id":"ENSG00000276052.1","gene_symbol":"RNU1-51P","gene_name":"RNA, U1 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:48393]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480163","summary":null,"start":189709539,"end":189709714,"strand":-1,"description":"RNA, U1 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:48393]"}, {"versioned_ensembl_gene_id":"ENSG00000221184.1","gene_symbol":"MIR1254-1","gene_name":"microRNA 1254-1 [Source:HGNC Symbol;Acc:HGNC:35319]","synonyms":"hsa-mir-1254,MIRN1254,MIR1254","biotype":"miRNA","ncbi_id":"100302273","summary":"This record was withdrawn by miRBase.","start":68759318,"end":68759414,"strand":1,"description":"microRNA 1254-1 [Source:HGNC Symbol;Acc:HGNC:35319]"}, {"versioned_ensembl_gene_id":"ENSG00000221514.1","gene_symbol":"SNORD111B","gene_name":"small nucleolar RNA, C/D box 111B [Source:HGNC Symbol;Acc:HGNC:33579]","synonyms":"MIR3647,hsa-mir-3647","biotype":"snoRNA","ncbi_id":"100113402","summary":null,"start":70529509,"end":70529588,"strand":1,"description":"small nucleolar RNA, C/D box 111B [Source:HGNC Symbol;Acc:HGNC:33579]"}, {"versioned_ensembl_gene_id":"ENSG00000238913.1","gene_symbol":"RNU7-196P","gene_name":"RNA, U7 small nuclear 196 pseudogene [Source:HGNC Symbol;Acc:HGNC:45730]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479098","summary":null,"start":73828012,"end":73828073,"strand":-1,"description":"RNA, U7 small nuclear 196 pseudogene [Source:HGNC Symbol;Acc:HGNC:45730]"}, {"versioned_ensembl_gene_id":"ENSG00000239194.1","gene_symbol":"RNU1-123P","gene_name":"RNA, U1 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:48465]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481628","summary":null,"start":67390691,"end":67390850,"strand":-1,"description":"RNA, U1 small nuclear 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:48465]"}, {"versioned_ensembl_gene_id":"ENSG00000199634.1","gene_symbol":"RNU4-79P","gene_name":"RNA, U4 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:47015]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481197","summary":null,"start":158395394,"end":158395534,"strand":1,"description":"RNA, U4 small nuclear 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:47015]"}, {"versioned_ensembl_gene_id":"ENSG00000222713.1","gene_symbol":"RN7SKP51","gene_name":"RNA, 7SK small nuclear pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:45775]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479117","summary":null,"start":117301455,"end":117301758,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:45775]"}, {"versioned_ensembl_gene_id":"ENSG00000212620.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":79843102,"end":79843228,"strand":1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000277625.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":15183174,"end":15183273,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280584.2","gene_symbol":"OBP2B","gene_name":"odorant binding protein 2B [Source:HGNC Symbol;Acc:HGNC:23381]","synonyms":"LCN14,hOBPIIb","biotype":"protein_coding","ncbi_id":"29989","summary":null,"start":133205277,"end":133209250,"strand":-1,"description":"odorant binding protein 2B [Source:HGNC Symbol;Acc:HGNC:23381]"}, {"versioned_ensembl_gene_id":"ENSG00000201351.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":90177222,"end":90177330,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252963.1","gene_symbol":"RN7SKP147","gene_name":"RNA, 7SK small nuclear pseudogene 147 [Source:HGNC Symbol;Acc:HGNC:45871]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480879","summary":null,"start":20356653,"end":20356896,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 147 [Source:HGNC Symbol;Acc:HGNC:45871]"}, {"versioned_ensembl_gene_id":"ENSG00000271222.1","gene_symbol":"AC091152.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44596346,"end":44597344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259968.3","gene_symbol":"AC093283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73952940,"end":73954014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237242.1","gene_symbol":"BTF3P15","gene_name":"basic transcription factor 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38567]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130409","summary":null,"start":109534655,"end":109534990,"strand":1,"description":"basic transcription factor 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38567]"}, {"versioned_ensembl_gene_id":"ENSG00000258896.1","gene_symbol":"SCOCP1","gene_name":"short coiled-coil protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317767","summary":null,"start":60158976,"end":60159324,"strand":1,"description":"short coiled-coil protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20339]"}, {"versioned_ensembl_gene_id":"ENSG00000220848.4","gene_symbol":"RPS18P9","gene_name":"ribosomal protein S18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36483]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645958","summary":null,"start":149594084,"end":149594543,"strand":1,"description":"ribosomal protein S18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36483]"}, {"versioned_ensembl_gene_id":"ENSG00000265135.1","gene_symbol":"MIR5687","gene_name":"microRNA 5687 [Source:HGNC Symbol;Acc:HGNC:43457]","synonyms":"hsa-mir-5687","biotype":"miRNA","ncbi_id":"100847019","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55508850,"end":55508926,"strand":-1,"description":"microRNA 5687 [Source:HGNC Symbol;Acc:HGNC:43457]"}, {"versioned_ensembl_gene_id":"ENSG00000199025.4","gene_symbol":"MIR369","gene_name":"microRNA 369 [Source:HGNC Symbol;Acc:HGNC:31783]","synonyms":"MIRN369,hsa-mir-369","biotype":"miRNA","ncbi_id":"442914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101065598,"end":101065667,"strand":1,"description":"microRNA 369 [Source:HGNC Symbol;Acc:HGNC:31783]"}, {"versioned_ensembl_gene_id":"ENSG00000283682.1","gene_symbol":"MIR548AH","gene_name":"microRNA 548ah [Source:HGNC Symbol;Acc:HGNC:41605]","synonyms":"hsa-mir-548ah","biotype":"miRNA","ncbi_id":"100616254","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76575551,"end":76575626,"strand":1,"description":"microRNA 548ah [Source:HGNC Symbol;Acc:HGNC:41605]"}, {"versioned_ensembl_gene_id":"ENSG00000264583.1","gene_symbol":"MIR4487","gene_name":"microRNA 4487 [Source:HGNC Symbol;Acc:HGNC:41851]","synonyms":"hsa-mir-4487","biotype":"miRNA","ncbi_id":"100616222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47400970,"end":47401042,"strand":1,"description":"microRNA 4487 [Source:HGNC Symbol;Acc:HGNC:41851]"}, {"versioned_ensembl_gene_id":"ENSG00000176928.5","gene_symbol":"GCNT4","gene_name":"glucosaminyl (N-acetyl) transferase 4, core 2 [Source:HGNC Symbol;Acc:HGNC:17973]","synonyms":"C2GNT3","biotype":"protein_coding","ncbi_id":"51301","summary":null,"start":75025346,"end":75030899,"strand":-1,"description":"glucosaminyl (N-acetyl) transferase 4, core 2 [Source:HGNC Symbol;Acc:HGNC:17973]"}, {"versioned_ensembl_gene_id":"ENSG00000249856.1","gene_symbol":"AC116337.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74917726,"end":75023928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265683.1","gene_symbol":"SYPL1P2","gene_name":"synaptophysin like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:53547]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132972","summary":null,"start":27351858,"end":27352584,"strand":-1,"description":"synaptophysin like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:53547]"}, {"versioned_ensembl_gene_id":"ENSG00000270049.2","gene_symbol":"AC009061.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67481314,"end":67505063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224437.2","gene_symbol":"PIGUP1","gene_name":"phosphatidylinositol glycan anchor biosynthesis class U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45158]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422342","summary":null,"start":70916997,"end":70917501,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45158]"}, {"versioned_ensembl_gene_id":"ENSG00000223597.2","gene_symbol":"LINC02142","gene_name":"long intergenic non-protein coding RNA 2142 [Source:HGNC Symbol;Acc:HGNC:53002]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374644","summary":null,"start":7373117,"end":7379790,"strand":1,"description":"long intergenic non-protein coding RNA 2142 [Source:HGNC Symbol;Acc:HGNC:53002]"}, {"versioned_ensembl_gene_id":"ENSG00000240103.2","gene_symbol":"AC132825.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22527324,"end":22529570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256618.2","gene_symbol":"MTRNR2L1","gene_name":"MT-RNR2-like 1 [Source:HGNC Symbol;Acc:HGNC:37155]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100462977","summary":null,"start":22523111,"end":22524663,"strand":1,"description":"MT-RNR2-like 1 [Source:HGNC Symbol;Acc:HGNC:37155]"}, {"versioned_ensembl_gene_id":"ENSG00000264168.2","gene_symbol":"MTND1P15","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42064]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288998","summary":null,"start":22524738,"end":22525686,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42064]"}, {"versioned_ensembl_gene_id":"ENSG00000265019.1","gene_symbol":"ABBA01006766.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22061961,"end":22070538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266979.1","gene_symbol":"LINC01180","gene_name":"long intergenic non-protein coding RNA 1180 [Source:HGNC Symbol;Acc:HGNC:49558]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927017","summary":null,"start":44646364,"end":44650349,"strand":-1,"description":"long intergenic non-protein coding RNA 1180 [Source:HGNC Symbol;Acc:HGNC:49558]"}, {"versioned_ensembl_gene_id":"ENSG00000267384.3","gene_symbol":"SMCO4P1","gene_name":"single-pass membrane protein with coiled-coil domains 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49559]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728675","summary":null,"start":44645411,"end":44645587,"strand":1,"description":"single-pass membrane protein with coiled-coil domains 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49559]"}, {"versioned_ensembl_gene_id":"ENSG00000182218.9","gene_symbol":"HHIPL1","gene_name":"HHIP like 1 [Source:HGNC Symbol;Acc:HGNC:19710]","synonyms":"KIAA1822","biotype":"protein_coding","ncbi_id":"84439","summary":"This gene encodes a protein that belongs to the glucose/sorbosone dehydrogenase family. The encoded protein also contains a domain that binds folate and reduced folic acid derivatives. [provided by RefSeq, Jul 2016]","start":99645110,"end":99680569,"strand":1,"description":"HHIP like 1 [Source:HGNC Symbol;Acc:HGNC:19710]"}, {"versioned_ensembl_gene_id":"ENSG00000229981.7","gene_symbol":"LINC01435","gene_name":"long intergenic non-protein coding RNA 1435 [Source:HGNC Symbol;Acc:HGNC:50753]","synonyms":"TCONS_00018040,RP11-215N21.1","biotype":"lincRNA","ncbi_id":"103695365","summary":null,"start":107694973,"end":108197849,"strand":-1,"description":"long intergenic non-protein coding RNA 1435 [Source:HGNC Symbol;Acc:HGNC:50753]"}, {"versioned_ensembl_gene_id":"ENSG00000213523.10","gene_symbol":"SRA1","gene_name":"steroid receptor RNA activator 1 [Source:HGNC Symbol;Acc:HGNC:11281]","synonyms":"STRAA1,SRA","biotype":"protein_coding","ncbi_id":"10011","summary":"Both long non-coding and protein-coding RNAs are transcribed from this gene, and they represent alternatively spliced transcript variants. This gene was initially defined as a non-coding RNA, which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer. It has now been found that this gene is involved in the regulation of many NR and non-NR activities, including metabolism, adipogenesis and chromatin organization. The long non-coding RNA transcripts interact with a variety of proteins, including the protein encoded by this gene. The encoded protein acts as a transcriptional repressor by binding to the non-coding RNA. [provided by RefSeq, Mar 2012]","start":140537340,"end":140558252,"strand":-1,"description":"steroid receptor RNA activator 1 [Source:HGNC Symbol;Acc:HGNC:11281]"}, {"versioned_ensembl_gene_id":"ENSG00000278876.1","gene_symbol":"AC145207.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81862778,"end":81863102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225663.7","gene_symbol":"MCRIP1","gene_name":"MAPK regulated corepressor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:28007]","synonyms":"MCRIP,GRAN2,FAM195B","biotype":"protein_coding","ncbi_id":"348262","summary":null,"start":81822361,"end":81833302,"strand":-1,"description":"MAPK regulated corepressor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:28007]"}, {"versioned_ensembl_gene_id":"ENSG00000183775.10","gene_symbol":"KCTD16","gene_name":"potassium channel tetramerization domain containing 16 [Source:HGNC Symbol;Acc:HGNC:29244]","synonyms":"KIAA1317","biotype":"protein_coding","ncbi_id":"57528","summary":null,"start":144170832,"end":144485686,"strand":1,"description":"potassium channel tetramerization domain containing 16 [Source:HGNC Symbol;Acc:HGNC:29244]"}, {"versioned_ensembl_gene_id":"ENSG00000250972.1","gene_symbol":"CKS1BP5","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:17640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526793","summary":null,"start":144439206,"end":144439478,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:17640]"}, {"versioned_ensembl_gene_id":"ENSG00000130711.3","gene_symbol":"PRDM12","gene_name":"PR/SET domain 12 [Source:HGNC Symbol;Acc:HGNC:13997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59335","summary":"This gene encodes a transcriptional regulator of sensory neuronal specification that plays a critical role in pain perception. The encoded protein contains an N-terminal PRDI-BF1 and RIZ homology (PR) domain, a SET domain, and three C-terminal C2H2 zinc finger DNA-binding domains. Naturally occurring mutations in this gene are associated with congenital insensitivity to pain (CIP), and hereditary sensory and autonomic neuropathies (HSAN's) affecting peripheral sensory and autonomic neurons. Deregulation of this gene is associated with solid cancers and hematological malignancies including chronic myeloid leukaemia. [provided by RefSeq, Mar 2017]","start":130664594,"end":130682981,"strand":1,"description":"PR/SET domain 12 [Source:HGNC Symbol;Acc:HGNC:13997]"}, {"versioned_ensembl_gene_id":"ENSG00000223505.2","gene_symbol":"AC114402.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203835585,"end":203835912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215644.9","gene_symbol":"GCGR","gene_name":"glucagon receptor [Source:HGNC Symbol;Acc:HGNC:4192]","synonyms":"GGR","biotype":"protein_coding","ncbi_id":"2642","summary":"The protein encoded by this gene is a glucagon receptor that is important in controlling blood glucose levels. Defects in this gene are a cause of non-insulin-dependent diabetes mellitus (NIDDM).[provided by RefSeq, Jan 2010]","start":81804132,"end":81814013,"strand":1,"description":"glucagon receptor [Source:HGNC Symbol;Acc:HGNC:4192]"}, {"versioned_ensembl_gene_id":"ENSG00000145817.16","gene_symbol":"YIPF5","gene_name":"Yip1 domain family member 5 [Source:HGNC Symbol;Acc:HGNC:24877]","synonyms":"SMAP-5,FinGER5","biotype":"protein_coding","ncbi_id":"81555","summary":null,"start":144158159,"end":144170714,"strand":-1,"description":"Yip1 domain family member 5 [Source:HGNC Symbol;Acc:HGNC:24877]"}, {"versioned_ensembl_gene_id":"ENSG00000149294.16","gene_symbol":"NCAM1","gene_name":"neural cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:7656]","synonyms":"NCAM,CD56","biotype":"protein_coding","ncbi_id":"4684","summary":"This gene encodes a cell adhesion protein which is a member of the immunoglobulin superfamily. The encoded protein is involved in cell-to-cell interactions as well as cell-matrix interactions during development and differentiation. The encoded protein plays a role in the development of the nervous system by regulating neurogenesis, neurite outgrowth, and cell migration. This protein is also involved in the expansion of T lymphocytes, B lymphocytes and natural killer (NK) cells which play an important role in immune surveillance. This protein plays a role in signal transduction by interacting with fibroblast growth factor receptors, N-cadherin and other components of the extracellular matrix and by triggering signalling cascades involving FYN-focal adhesion kinase (FAK), mitogen-activated protein kinase (MAPK), and phosphatidylinositol 3-kinase (PI3K). One prominent isoform of this gene, cell surface molecule CD56, plays a role in several myeloproliferative disorders such as acute myeloid leukemia and differential expression of this gene is associated with differential disease progression. For example, increased expression of CD56 is correlated with lower survival in acute myeloid leukemia patients whereas increased severity of COVID-19 is correlated with decreased abundance of CD56-expressing NK cells in peripheral blood. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Aug 2020]","start":112961247,"end":113278436,"strand":1,"description":"neural cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:7656]"}, {"versioned_ensembl_gene_id":"ENSG00000232300.1","gene_symbol":"FAM215B","gene_name":"family with sequence similarity 215 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43639]","synonyms":"ARL17A-IT1","biotype":"lincRNA","ncbi_id":"644297","summary":null,"start":46558830,"end":46562795,"strand":-1,"description":"family with sequence similarity 215 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43639]"}, {"versioned_ensembl_gene_id":"ENSG00000183048.11","gene_symbol":"SLC25A10","gene_name":"solute carrier family 25 member 10 [Source:HGNC Symbol;Acc:HGNC:10980]","synonyms":"DIC","biotype":"protein_coding","ncbi_id":"1468","summary":"This gene encodes a member of a family of proteins that translocate small metabolites across the mitochondrial membrane. The encoded protein exchanges dicarboxylates, such as malate and succinate, for phosphate, sulfate, and other small molecules, thereby providing substrates for metabolic processes including the Krebs cycle and fatty acid synthesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":81712236,"end":81721016,"strand":1,"description":"solute carrier family 25 member 10 [Source:HGNC Symbol;Acc:HGNC:10980]"}, {"versioned_ensembl_gene_id":"ENSG00000185829.17","gene_symbol":"ARL17A","gene_name":"ADP ribosylation factor like GTPase 17A [Source:HGNC Symbol;Acc:HGNC:24096]","synonyms":"ARL17P1,ARF1P2","biotype":"protein_coding","ncbi_id":"51326","summary":null,"start":46516702,"end":46579682,"strand":-1,"description":"ADP ribosylation factor like GTPase 17A [Source:HGNC Symbol;Acc:HGNC:24096]"}, {"versioned_ensembl_gene_id":"ENSG00000238083.7","gene_symbol":"LRRC37A2","gene_name":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]","synonyms":"FLJ45049,FLJ45049","biotype":"protein_coding","ncbi_id":"474170","summary":null,"start":46511511,"end":46555650,"strand":1,"description":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]"}, {"versioned_ensembl_gene_id":"ENSG00000158497.3","gene_symbol":"HMHB1","gene_name":"histocompatibility minor HB-1 [Source:HGNC Symbol;Acc:HGNC:29677]","synonyms":"HB-1Y,HB-1","biotype":"protein_coding","ncbi_id":"57824","summary":"This gene encodes one of the minor histocompatibility antigens, which play an important role in the induction of cytotoxic T lymphocyte (CTL) reactivity against leukemia after human histocompatibility leukocyte antigen (HLA)-identical allogeneic bone marrow transplantation (BMT). This gene is only expressed in B cell acute lymphoblastic leukemia cells and Epstein-Barr virus-transformed B cells. The translation of this mRNA initiates at a non-AUG (CUG) codon. [provided by RefSeq, Jul 2008]","start":143812161,"end":143820719,"strand":1,"description":"histocompatibility minor HB-1 [Source:HGNC Symbol;Acc:HGNC:29677]"}, {"versioned_ensembl_gene_id":"ENSG00000225869.4","gene_symbol":"AC008696.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143752090,"end":143752704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218454.2","gene_symbol":"HNRNPA1P19","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39537]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874402","summary":null,"start":20771058,"end":20771427,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39537]"}, {"versioned_ensembl_gene_id":"ENSG00000262877.4","gene_symbol":"AC110285.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81388126,"end":81390256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214087.8","gene_symbol":"ARL16","gene_name":"ADP ribosylation factor like GTPase 16 [Source:HGNC Symbol;Acc:HGNC:27902]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339231","summary":"The protein encoded by this gene belongs to the ARL (ADP-ribosylation factor-like) family of proteins, which are structurally related to ADP-ribosylation factors (ARFs). This protein has been shown to have an inhibitory role in the cellular antiviral response. This gene product interacts with the C-terminal domain of the DEXD/H-box helicase 58 (DDX58) gene product. This interaction was found to suppress the association between the DDX58 gene product and RNA, thereby negatively regulating the activity of the DDX58 gene product. [provided by RefSeq, Jul 2016]","start":81681174,"end":81683924,"strand":-1,"description":"ADP ribosylation factor like GTPase 16 [Source:HGNC Symbol;Acc:HGNC:27902]"}, {"versioned_ensembl_gene_id":"ENSG00000244691.1","gene_symbol":"RPL10AP1","gene_name":"ribosomal protein L10a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19813]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319135","summary":null,"start":103412119,"end":103412761,"strand":-1,"description":"ribosomal protein L10a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19813]"}, {"versioned_ensembl_gene_id":"ENSG00000254626.1","gene_symbol":"AP003100.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112787304,"end":112795854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255484.2","gene_symbol":"AP003063.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112534220,"end":112555802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250303.3","gene_symbol":"AP002884.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112270749,"end":112362534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255883.1","gene_symbol":"FUNDC2P1","gene_name":"FUN14 domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17253]","synonyms":"FUNDC2P","biotype":"processed_pseudogene","ncbi_id":"220793","summary":null,"start":73508685,"end":73509254,"strand":1,"description":"FUN14 domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17253]"}, {"versioned_ensembl_gene_id":"ENSG00000262049.1","gene_symbol":"AC139530.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81701324,"end":81703300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185298.12","gene_symbol":"CCDC137","gene_name":"coiled-coil domain containing 137 [Source:HGNC Symbol;Acc:HGNC:33451]","synonyms":"MGC16597","biotype":"protein_coding","ncbi_id":"339230","summary":null,"start":81666364,"end":81673904,"strand":1,"description":"coiled-coil domain containing 137 [Source:HGNC Symbol;Acc:HGNC:33451]"}, {"versioned_ensembl_gene_id":"ENSG00000204237.4","gene_symbol":"OXLD1","gene_name":"oxidoreductase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27901]","synonyms":"MGC104712,C17orf90","biotype":"protein_coding","ncbi_id":"339229","summary":null,"start":81665036,"end":81666635,"strand":-1,"description":"oxidoreductase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27901]"}, {"versioned_ensembl_gene_id":"ENSG00000185527.11","gene_symbol":"PDE6G","gene_name":"phosphodiesterase 6G [Source:HGNC Symbol;Acc:HGNC:8789]","synonyms":"RP57,PDEG","biotype":"protein_coding","ncbi_id":"5148","summary":"This gene encodes the gamma subunit of cyclic GMP-phosphodiesterase, which is composed of alpha- and beta- catalytic subunits and two identical, inhibitory gamma subunits. This gene is expressed in rod photoreceptors and functions in the phototransduction signaling cascade. It is also expressed in a variety of other tissues, and has been shown to regulate the c-Src protein kinase and G-protein-coupled receptor kinase 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009]","start":81650459,"end":81663112,"strand":-1,"description":"phosphodiesterase 6G [Source:HGNC Symbol;Acc:HGNC:8789]"}, {"versioned_ensembl_gene_id":"ENSG00000258749.1","gene_symbol":"AL110504.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99512501,"end":99513576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251143.1","gene_symbol":"AP002490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72014291,"end":72020910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182446.13","gene_symbol":"NPLOC4","gene_name":"NPL4 homolog, ubiquitin recognition factor [Source:HGNC Symbol;Acc:HGNC:18261]","synonyms":"NPL4,KIAA1499,FLJ20657","biotype":"protein_coding","ncbi_id":"55666","summary":null,"start":81556887,"end":81648465,"strand":-1,"description":"NPL4 homolog, ubiquitin recognition factor [Source:HGNC Symbol;Acc:HGNC:18261]"}, {"versioned_ensembl_gene_id":"ENSG00000150787.7","gene_symbol":"PTS","gene_name":"6-pyruvoyltetrahydropterin synthase [Source:HGNC Symbol;Acc:HGNC:9689]","synonyms":"PTPS","biotype":"protein_coding","ncbi_id":"5805","summary":"The enzyme encoded by this gene catalyzes the elimination of inorganic triphosphate from dihydroneopterin triphosphate, which is the second and irreversible step in the biosynthesis of tetrahydrobiopterin from GTP. Tetrahydrobiopterin, also known as BH(4), is an essential cofactor and regulator of various enzyme activities, including enzymes involved in serotonin biosynthesis and NO synthase activity. Mutations in this gene result in hyperphenylalaninemia. [provided by RefSeq, Oct 2008]","start":112226365,"end":112269955,"strand":1,"description":"6-pyruvoyltetrahydropterin synthase [Source:HGNC Symbol;Acc:HGNC:9689]"}, {"versioned_ensembl_gene_id":"ENSG00000268472.2","gene_symbol":"AP002884.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112260265,"end":112261396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233098.8","gene_symbol":"CCDC144NL-AS1","gene_name":"CCDC144NL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51340]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"440416","summary":null,"start":20868433,"end":21002276,"strand":1,"description":"CCDC144NL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51340]"}, {"versioned_ensembl_gene_id":"ENSG00000266009.1","gene_symbol":"AC087393.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20981489,"end":20981654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244456.2","gene_symbol":"AC090774.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20956682,"end":20958404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264660.2","gene_symbol":"AC107926.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20963722,"end":20980238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205212.3","gene_symbol":"CCDC144NL","gene_name":"coiled-coil domain containing 144 family, N-terminal like [Source:HGNC Symbol;Acc:HGNC:33735]","synonyms":"MGC87631","biotype":"protein_coding","ncbi_id":"339184","summary":null,"start":20836447,"end":20896140,"strand":-1,"description":"coiled-coil domain containing 144 family, N-terminal like [Source:HGNC Symbol;Acc:HGNC:33735]"}, {"versioned_ensembl_gene_id":"ENSG00000124422.11","gene_symbol":"USP22","gene_name":"ubiquitin specific peptidase 22 [Source:HGNC Symbol;Acc:HGNC:12621]","synonyms":"USP3L,KIAA1063","biotype":"protein_coding","ncbi_id":"23326","summary":null,"start":20999593,"end":21043760,"strand":-1,"description":"ubiquitin specific peptidase 22 [Source:HGNC Symbol;Acc:HGNC:12621]"}, {"versioned_ensembl_gene_id":"ENSG00000229848.1","gene_symbol":"AC139149.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81514047,"end":81527776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260075.1","gene_symbol":"AC217777.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46372855,"end":46487141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279692.1","gene_symbol":"AC110285.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81395609,"end":81397144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263271.1","gene_symbol":"AC110285.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81461013,"end":81461937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145741.15","gene_symbol":"BTF3","gene_name":"basic transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:1125]","synonyms":"NACB,BTF3b,BTF3a","biotype":"protein_coding","ncbi_id":"689","summary":"This gene encodes the basic transcription factor 3. This protein forms a stable complex with RNA polymerase IIB and is required for transcriptional initiation. Alternative splicing results in multiple transcript variants encoding different isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Jul 2008]","start":73498408,"end":73505635,"strand":1,"description":"basic transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:1125]"}, {"versioned_ensembl_gene_id":"ENSG00000264662.1","gene_symbol":"AC126365.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20789217,"end":20789595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264215.1","gene_symbol":"AC126365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20788071,"end":20789584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226549.3","gene_symbol":"SCDP1","gene_name":"stearoyl-CoA desaturase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10572]","synonyms":"SCDP","biotype":"processed_pseudogene","ncbi_id":"645313","summary":null,"start":20784645,"end":20785725,"strand":1,"description":"stearoyl-CoA desaturase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10572]"}, {"versioned_ensembl_gene_id":"ENSG00000108312.14","gene_symbol":"UBTF","gene_name":"upstream binding transcription factor, RNA polymerase I [Source:HGNC Symbol;Acc:HGNC:12511]","synonyms":"UBF2,UBF1,UBF,NOR-90","biotype":"protein_coding","ncbi_id":"7343","summary":"This gene encodes a member of the HMG-box DNA-binding protein family. The encoded protein plays a critical role in ribosomal RNA transcription as a key component of the pre-initiation complex, mediating the recruitment of RNA polymerase I to rDNA promoter regions. The encoded protein may also play important roles in chromatin remodeling and pre-rRNA processing, and its activity is regulated by both phosphorylation and acetylation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Pseudogenes of this gene are located on the short arm of chromosomes 3, 11 and X and the long arm of chromosome 11. [provided by RefSeq, Aug 2011]","start":44205033,"end":44221626,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I [Source:HGNC Symbol;Acc:HGNC:12511]"}, {"versioned_ensembl_gene_id":"ENSG00000215002.2","gene_symbol":"RPL23AP59","gene_name":"ribosomal protein L23a pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:36920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271618","summary":null,"start":106550106,"end":106551121,"strand":1,"description":"ribosomal protein L23a pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:36920]"}, {"versioned_ensembl_gene_id":"ENSG00000272525.1","gene_symbol":"AC099522.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73497550,"end":73498293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130707.17","gene_symbol":"ASS1","gene_name":"argininosuccinate synthase 1 [Source:HGNC Symbol;Acc:HGNC:758]","synonyms":"CTLN1,ASS","biotype":"protein_coding","ncbi_id":"445","summary":"The protein encoded by this gene catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 copies of this gene including the pseudogenes scattered across the human genome, among which the one located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. Mutations in the chromosome 9 copy of this gene cause citrullinemia. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2012]","start":130444929,"end":130501274,"strand":1,"description":"argininosuccinate synthase 1 [Source:HGNC Symbol;Acc:HGNC:758]"}, {"versioned_ensembl_gene_id":"ENSG00000185332.6","gene_symbol":"TMEM105","gene_name":"transmembrane protein 105 [Source:HGNC Symbol;Acc:HGNC:26794]","synonyms":"FLJ38792","biotype":"protein_coding","ncbi_id":"284186","summary":null,"start":81311270,"end":81330674,"strand":-1,"description":"transmembrane protein 105 [Source:HGNC Symbol;Acc:HGNC:26794]"}, {"versioned_ensembl_gene_id":"ENSG00000185168.5","gene_symbol":"LINC00482","gene_name":"long intergenic non-protein coding RNA 482 [Source:HGNC Symbol;Acc:HGNC:26816]","synonyms":"FLJ39421,C17orf55","biotype":"lincRNA","ncbi_id":"284185","summary":null,"start":81303771,"end":81309248,"strand":-1,"description":"long intergenic non-protein coding RNA 482 [Source:HGNC Symbol;Acc:HGNC:26816]"}, {"versioned_ensembl_gene_id":"ENSG00000229466.1","gene_symbol":"AL731574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105808775,"end":105819197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276101.1","gene_symbol":"AC027601.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81251194,"end":81251803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231579.3","gene_symbol":"RPL7P21","gene_name":"ribosomal protein L7 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729123","summary":null,"start":143332605,"end":143333239,"strand":1,"description":"ribosomal protein L7 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36762]"}, {"versioned_ensembl_gene_id":"ENSG00000087152.15","gene_symbol":"ATXN7L3","gene_name":"ataxin 7 like 3 [Source:HGNC Symbol;Acc:HGNC:25416]","synonyms":"DKFZp761G2113","biotype":"protein_coding","ncbi_id":"56970","summary":null,"start":44191805,"end":44200113,"strand":-1,"description":"ataxin 7 like 3 [Source:HGNC Symbol;Acc:HGNC:25416]"}, {"versioned_ensembl_gene_id":"ENSG00000251493.4","gene_symbol":"FOXD1","gene_name":"forkhead box D1 [Source:HGNC Symbol;Acc:HGNC:3802]","synonyms":"FREAC4,FKHL8","biotype":"protein_coding","ncbi_id":"2297","summary":"This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. Studies of the orthologous mouse protein indicate that it functions in kidney development by promoting nephron progenitor differentiation, and it also functions in the development of the retina and optic chiasm. It may also regulate inflammatory reactions and prevent autoimmunity. [provided by RefSeq, Apr 2014]","start":73444827,"end":73448527,"strand":-1,"description":"forkhead box D1 [Source:HGNC Symbol;Acc:HGNC:3802]"}, {"versioned_ensembl_gene_id":"ENSG00000226096.1","gene_symbol":"AC087499.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20609462,"end":20609610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165059.7","gene_symbol":"PRKACG","gene_name":"protein kinase cAMP-activated catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9382]","synonyms":"PKACg","biotype":"protein_coding","ncbi_id":"5568","summary":"Cyclic AMP-dependent protein kinase (PKA) consists of two catalytic subunits and a regulatory subunit dimer. This gene encodes the gamma form of its catalytic subunit. The gene is intronless and is thought to be a retrotransposon derived from the gene for the alpha form of the PKA catalytic subunit. [provided by RefSeq, Jul 2008]","start":69012529,"end":69014113,"strand":-1,"description":"protein kinase cAMP-activated catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9382]"}, {"versioned_ensembl_gene_id":"ENSG00000161664.6","gene_symbol":"ASB16","gene_name":"ankyrin repeat and SOCS box containing 16 [Source:HGNC Symbol;Acc:HGNC:19768]","synonyms":"FLJ30165","biotype":"protein_coding","ncbi_id":"92591","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and a SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. [provided by RefSeq, Jul 2008]","start":44170447,"end":44179083,"strand":1,"description":"ankyrin repeat and SOCS box containing 16 [Source:HGNC Symbol;Acc:HGNC:19768]"}, {"versioned_ensembl_gene_id":"ENSG00000231233.1","gene_symbol":"CFAP58-AS1","gene_name":"CFAP58 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45243]","synonyms":"CCDC147-AS1","biotype":"antisense_RNA","ncbi_id":"100505869","summary":null,"start":104351591,"end":104353575,"strand":-1,"description":"CFAP58 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45243]"}, {"versioned_ensembl_gene_id":"ENSG00000165506.14","gene_symbol":"DNAAF2","gene_name":"dynein axonemal assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:20188]","synonyms":"FLJ10563,CILD10,C14orf104,PF13,KTU","biotype":"protein_coding","ncbi_id":"55172","summary":"This gene encodes a highly conserved protein involved in the preassembly of dynein arm complexes which power cilia. These complexes are found in some cilia and are assembled in the cytoplasm prior to transport for cilia formation. Mutations in this gene have been associated with primary ciliary dyskinesia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":49625174,"end":49635230,"strand":-1,"description":"dynein axonemal assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:20188]"}, {"versioned_ensembl_gene_id":"ENSG00000258450.1","gene_symbol":"AL139099.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49629291,"end":49629890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175866.15","gene_symbol":"BAIAP2","gene_name":"BAI1 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:947]","synonyms":"IRSp53,BAP2","biotype":"protein_coding","ncbi_id":"10458","summary":"The protein encoded by this gene has been identified as a brain-specific angiogenesis inhibitor (BAI1)-binding protein. This adaptor protein links membrane bound G-proteins to cytoplasmic effector proteins. This protein functions as an insulin receptor tyrosine kinase substrate and suggests a role for insulin in the central nervous system. It also associates with a downstream effector of Rho small G proteins, which is associated with the formation of stress fibers and cytokinesis. This protein is involved in lamellipodia and filopodia formation in motile cells and may affect neuronal growth-cone guidance. This protein has also been identified as interacting with the dentatorubral-pallidoluysian atrophy gene, which is associated with an autosomal dominant neurodegenerative disease. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jan 2009]","start":81035122,"end":81117432,"strand":1,"description":"BAI1 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:947]"}, {"versioned_ensembl_gene_id":"ENSG00000259428.1","gene_symbol":"HMGB3P26","gene_name":"high mobility group box 3 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39318]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130405","summary":null,"start":103364239,"end":103364820,"strand":-1,"description":"high mobility group box 3 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39318]"}, {"versioned_ensembl_gene_id":"ENSG00000279586.1","gene_symbol":"AP000711.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":117611101,"end":117612017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258702.1","gene_symbol":"AL137786.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96592733,"end":96595762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258979.1","gene_symbol":"LINC02299","gene_name":"long intergenic non-protein coding RNA 2299 [Source:HGNC Symbol;Acc:HGNC:53218]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370646","summary":null,"start":96741191,"end":96790613,"strand":1,"description":"long intergenic non-protein coding RNA 2299 [Source:HGNC Symbol;Acc:HGNC:53218]"}, {"versioned_ensembl_gene_id":"ENSG00000262662.1","gene_symbol":"AC127496.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80960766,"end":80961713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261924.1","gene_symbol":"AC127496.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80966239,"end":80971213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231645.2","gene_symbol":"KRT17P6","gene_name":"keratin 17 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50724]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284196","summary":null,"start":20512560,"end":20517479,"strand":-1,"description":"keratin 17 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50724]"}, {"versioned_ensembl_gene_id":"ENSG00000259376.1","gene_symbol":"AC090907.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101043716,"end":101049456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167291.15","gene_symbol":"TBC1D16","gene_name":"TBC1 domain family member 16 [Source:HGNC Symbol;Acc:HGNC:28356]","synonyms":"MGC25062,FLJ20748","biotype":"protein_coding","ncbi_id":"125058","summary":null,"start":79932343,"end":80035848,"strand":-1,"description":"TBC1 domain family member 16 [Source:HGNC Symbol;Acc:HGNC:28356]"}, {"versioned_ensembl_gene_id":"ENSG00000248708.1","gene_symbol":"LINC02144","gene_name":"long intergenic non-protein coding RNA 2144 [Source:HGNC Symbol;Acc:HGNC:53004]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379069","summary":null,"start":87713135,"end":87733269,"strand":-1,"description":"long intergenic non-protein coding RNA 2144 [Source:HGNC Symbol;Acc:HGNC:53004]"}, {"versioned_ensembl_gene_id":"ENSG00000275516.1","gene_symbol":"AC100791.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79952663,"end":79952992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160352.15","gene_symbol":"ZNF714","gene_name":"zinc finger protein 714 [Source:HGNC Symbol;Acc:HGNC:27124]","synonyms":null,"biotype":"protein_coding","ncbi_id":"148206","summary":null,"start":21082159,"end":21125270,"strand":1,"description":"zinc finger protein 714 [Source:HGNC Symbol;Acc:HGNC:27124]"}, {"versioned_ensembl_gene_id":"ENSG00000173821.19","gene_symbol":"RNF213","gene_name":"ring finger protein 213 [Source:HGNC Symbol;Acc:HGNC:14539]","synonyms":"NET57,MYMY2,KIAA1618,KIAA1554,C17orf27","biotype":"protein_coding","ncbi_id":"57674","summary":"This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":80260866,"end":80398786,"strand":1,"description":"ring finger protein 213 [Source:HGNC Symbol;Acc:HGNC:14539]"}, {"versioned_ensembl_gene_id":"ENSG00000280248.1","gene_symbol":"AC124319.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80339898,"end":80342058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133063.15","gene_symbol":"CHIT1","gene_name":"chitinase 1 [Source:HGNC Symbol;Acc:HGNC:1936]","synonyms":"CHIT,CHI3","biotype":"protein_coding","ncbi_id":"1118","summary":"Chitotriosidase is secreted by activated human macrophages and is markedly elevated in plasma of Gaucher disease patients. The expression of chitotriosidase occurs only at a late stage of differentiation of monocytes to activated macrophages in culture. Human macrophages can synthesize a functional chitotriosidase, a highly conserved enzyme with a strongly regulated expression. This enzyme may play a role in the degradation of chitin-containing pathogens. Several alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jan 2012]","start":203212827,"end":203273641,"strand":-1,"description":"chitinase 1 [Source:HGNC Symbol;Acc:HGNC:1936]"}, {"versioned_ensembl_gene_id":"ENSG00000196979.1","gene_symbol":"AL360004.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130140610,"end":130144219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181778.4","gene_symbol":"TMEM252","gene_name":"transmembrane protein 252 [Source:HGNC Symbol;Acc:HGNC:28537]","synonyms":"MGC34760,C9orf71","biotype":"protein_coding","ncbi_id":"169693","summary":null,"start":68536580,"end":68540867,"strand":-1,"description":"transmembrane protein 252 [Source:HGNC Symbol;Acc:HGNC:28537]"}, {"versioned_ensembl_gene_id":"ENSG00000156603.16","gene_symbol":"MED19","gene_name":"mediator complex subunit 19 [Source:HGNC Symbol;Acc:HGNC:29600]","synonyms":"LCMR1","biotype":"protein_coding","ncbi_id":"219541","summary":"The protein encoded by this gene is a subunit of the Mediator complex, which binds to gene-specific regulatory factors and provides support for the basal RNA polymerase II transcription machinery. This gene has been implicated in the growth of several types of cancer, and inhibition of its expression inhibits the growth and spread of these cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":57703714,"end":57712323,"strand":-1,"description":"mediator complex subunit 19 [Source:HGNC Symbol;Acc:HGNC:29600]"}, {"versioned_ensembl_gene_id":"ENSG00000258751.1","gene_symbol":"AL358335.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48396508,"end":48491767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242417.1","gene_symbol":"RPL18P1","gene_name":"ribosomal protein L18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19673]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326291","summary":null,"start":48489883,"end":48490434,"strand":1,"description":"ribosomal protein L18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19673]"}, {"versioned_ensembl_gene_id":"ENSG00000230528.7","gene_symbol":"NOS2P3","gene_name":"nitric oxide synthase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35124]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339256","summary":null,"start":20436337,"end":20447249,"strand":1,"description":"nitric oxide synthase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35124]"}, {"versioned_ensembl_gene_id":"ENSG00000156599.10","gene_symbol":"ZDHHC5","gene_name":"zinc finger DHHC-type containing 5 [Source:HGNC Symbol;Acc:HGNC:18472]","synonyms":"ZNF375,KIAA1748,DHHC5","biotype":"protein_coding","ncbi_id":"25921","summary":null,"start":57667747,"end":57701187,"strand":1,"description":"zinc finger DHHC-type containing 5 [Source:HGNC Symbol;Acc:HGNC:18472]"}, {"versioned_ensembl_gene_id":"ENSG00000278071.1","gene_symbol":"AL161669.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103208100,"end":103208876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256563.2","gene_symbol":"NANOGNBP2","gene_name":"NANOGNB pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42159]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060006","summary":null,"start":132972338,"end":132972890,"strand":-1,"description":"NANOGNB pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42159]"}, {"versioned_ensembl_gene_id":"ENSG00000224261.2","gene_symbol":"RPSAP18","gene_name":"ribosomal protein SA pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36106]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388707","summary":null,"start":160266340,"end":160267225,"strand":-1,"description":"ribosomal protein SA pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36106]"}, {"versioned_ensembl_gene_id":"ENSG00000216921.7","gene_symbol":"AC131097.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":241893985,"end":241902551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259374.2","gene_symbol":"NDUFB4P11","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:45259]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"107075247","summary":null,"start":103139675,"end":103141959,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:45259]"}, {"versioned_ensembl_gene_id":"ENSG00000065618.18","gene_symbol":"COL17A1","gene_name":"collagen type XVII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2194]","synonyms":"BPAG2,BP180","biotype":"protein_coding","ncbi_id":"1308","summary":"This gene encodes the alpha chain of type XVII collagen. Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in this gene are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD-1, is generated by proteolytic processing of the full length form. [provided by RefSeq, Jul 2008]","start":104031286,"end":104086002,"strand":-1,"description":"collagen type XVII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2194]"}, {"versioned_ensembl_gene_id":"ENSG00000164180.13","gene_symbol":"TMEM161B","gene_name":"transmembrane protein 161B [Source:HGNC Symbol;Acc:HGNC:28483]","synonyms":"MGC33214","biotype":"protein_coding","ncbi_id":"153396","summary":null,"start":88189633,"end":88269476,"strand":-1,"description":"transmembrane protein 161B [Source:HGNC Symbol;Acc:HGNC:28483]"}, {"versioned_ensembl_gene_id":"ENSG00000250306.1","gene_symbol":"AC091826.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88382948,"end":88383260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275479.1","gene_symbol":"AC087741.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80149627,"end":80149798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141543.9","gene_symbol":"EIF4A3","gene_name":"eukaryotic translation initiation factor 4A3 [Source:HGNC Symbol;Acc:HGNC:18683]","synonyms":"KIAA0111,Fal1,EIF4AIII,DDX48","biotype":"protein_coding","ncbi_id":"9775","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a nuclear matrix protein. Its amino acid sequence is highly similar to the amino acid sequences of the translation initiation factors eIF4AI and eIF4AII, two other members of the DEAD box protein family. [provided by RefSeq, Jul 2008]","start":80135214,"end":80147183,"strand":-1,"description":"eukaryotic translation initiation factor 4A3 [Source:HGNC Symbol;Acc:HGNC:18683]"}, {"versioned_ensembl_gene_id":"ENSG00000225297.1","gene_symbol":"AC126124.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93199755,"end":93199939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122180.4","gene_symbol":"MYOG","gene_name":"myogenin [Source:HGNC Symbol;Acc:HGNC:7612]","synonyms":"MYF4,bHLHc3","biotype":"protein_coding","ncbi_id":"4656","summary":"Myogenin is a muscle-specific transcription factor that can induce myogenesis in a variety of cell types in tissue culture. It is a member of a large family of proteins related by sequence homology, the helix-loop-helix (HLH) proteins. It is essential for the development of functional skeletal muscle. [provided by RefSeq, Jul 2008]","start":203083132,"end":203086036,"strand":-1,"description":"myogenin [Source:HGNC Symbol;Acc:HGNC:7612]"}, {"versioned_ensembl_gene_id":"ENSG00000267519.5","gene_symbol":"AC020916.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13834516,"end":13836289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267090.1","gene_symbol":"AC005789.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38385522,"end":38386759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182156.9","gene_symbol":"ENPP7","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 [Source:HGNC Symbol;Acc:HGNC:23764]","synonyms":"NPP7,alk-SMase","biotype":"protein_coding","ncbi_id":"339221","summary":"The protein encoded by this gene is an intestinal alkaline sphingomyelin phosphodiesterase that converts sphingomyelin to ceramide and phosphocholine. The encoded protein is anchored in the cell membrane, and it may function to protect the intestinal mucosa from inflammation and tumorigenesis. This protein is glycosylated and also exhibits lysophosphatidylcholine hydrolase activity. [provided by RefSeq, Oct 2016]","start":79730919,"end":79742222,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 [Source:HGNC Symbol;Acc:HGNC:23764]"}, {"versioned_ensembl_gene_id":"ENSG00000123610.4","gene_symbol":"TNFAIP6","gene_name":"TNF alpha induced protein 6 [Source:HGNC Symbol;Acc:HGNC:11898]","synonyms":"TSG6,TSG-6","biotype":"protein_coding","ncbi_id":"7130","summary":"The protein encoded by this gene is a secretory protein that contains a hyaluronan-binding domain, and thus is a member of the hyaluronan-binding protein family. The hyaluronan-binding domain is known to be involved in extracellular matrix stability and cell migration. This protein has been shown to form a stable complex with inter-alpha-inhibitor (I alpha I), and thus enhance the serine protease inhibitory activity of I alpha I, which is important in the protease network associated with inflammation. This gene can be induced by proinflammatory cytokines such as tumor necrosis factor alpha and interleukin-1. Enhanced levels of this protein are found in the synovial fluid of patients with osteoarthritis and rheumatoid arthritis.[provided by RefSeq, Dec 2010]","start":151357592,"end":151380048,"strand":1,"description":"TNF alpha induced protein 6 [Source:HGNC Symbol;Acc:HGNC:11898]"}, {"versioned_ensembl_gene_id":"ENSG00000130045.15","gene_symbol":"NXNL2","gene_name":"nucleoredoxin like 2 [Source:HGNC Symbol;Acc:HGNC:30482]","synonyms":"RdCVF2,C9orf121","biotype":"protein_coding","ncbi_id":"158046","summary":null,"start":88535101,"end":88584274,"strand":1,"description":"nucleoredoxin like 2 [Source:HGNC Symbol;Acc:HGNC:30482]"}, {"versioned_ensembl_gene_id":"ENSG00000228189.4","gene_symbol":"AL592486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88627189,"end":88652160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259515.1","gene_symbol":"AL117209.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102933574,"end":102937177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166126.10","gene_symbol":"AMN","gene_name":"amnion associated transmembrane protein [Source:HGNC Symbol;Acc:HGNC:14604]","synonyms":"amnionless","biotype":"protein_coding","ncbi_id":"81693","summary":"The protein encoded by this gene is a type I transmembrane protein. It is thought to modulate bone morphogenetic protein (BMP) receptor function by serving as an accessory or coreceptor, and thus facilitates or hinders BMP binding. It is known that the mouse AMN gene is expressed in the extraembryonic visceral endoderm layer during gastrulation, but it is found to be mutated in amnionless mouse. The encoded protein has sequence similarity to short gastrulation (Sog) and procollagen IIA proteins in Drosophila. [provided by RefSeq, Jul 2008]","start":102922656,"end":102933596,"strand":1,"description":"amnion associated transmembrane protein [Source:HGNC Symbol;Acc:HGNC:14604]"}, {"versioned_ensembl_gene_id":"ENSG00000213176.4","gene_symbol":"RPL13P6","gene_name":"ribosomal protein L13 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19809]","synonyms":"RPL13AP4","biotype":"processed_pseudogene","ncbi_id":"100129176","summary":null,"start":103041469,"end":103042094,"strand":1,"description":"ribosomal protein L13 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19809]"}, {"versioned_ensembl_gene_id":"ENSG00000162777.16","gene_symbol":"DENND2D","gene_name":"DENN domain containing 2D [Source:HGNC Symbol;Acc:HGNC:26192]","synonyms":"RP5-1180E21.2,FLJ22457","biotype":"protein_coding","ncbi_id":"79961","summary":null,"start":111187174,"end":111204535,"strand":-1,"description":"DENN domain containing 2D [Source:HGNC Symbol;Acc:HGNC:26192]"}, {"versioned_ensembl_gene_id":"ENSG00000035862.12","gene_symbol":"TIMP2","gene_name":"TIMP metallopeptidase inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:11821]","synonyms":"CSC-21K","biotype":"protein_coding","ncbi_id":"7077","summary":"This gene is a member of the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. In addition to an inhibitory role against metalloproteinases, the encoded protein has a unique role among TIMP family members in its ability to directly suppress the proliferation of endothelial cells. As a result, the encoded protein may be critical to the maintenance of tissue homeostasis by suppressing the proliferation of quiescent tissues in response to angiogenic factors, and by inhibiting protease activity in tissues undergoing remodelling of the extracellular matrix. [provided by RefSeq, Jul 2008]","start":78852977,"end":78925387,"strand":-1,"description":"TIMP metallopeptidase inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:11821]"}, {"versioned_ensembl_gene_id":"ENSG00000267355.2","gene_symbol":"AC022966.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78845953,"end":78846868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164576.11","gene_symbol":"SAP30L","gene_name":"SAP30 like [Source:HGNC Symbol;Acc:HGNC:25663]","synonyms":"NS4ATP2,FLJ11526","biotype":"protein_coding","ncbi_id":"79685","summary":null,"start":154445957,"end":154461054,"strand":1,"description":"SAP30 like [Source:HGNC Symbol;Acc:HGNC:25663]"}, {"versioned_ensembl_gene_id":"ENSG00000070190.12","gene_symbol":"DAPP1","gene_name":"dual adaptor of phosphotyrosine and 3-phosphoinositides 1 [Source:HGNC Symbol;Acc:HGNC:16500]","synonyms":"BAM32","biotype":"protein_coding","ncbi_id":"27071","summary":null,"start":99816833,"end":99870154,"strand":1,"description":"dual adaptor of phosphotyrosine and 3-phosphoinositides 1 [Source:HGNC Symbol;Acc:HGNC:16500]"}, {"versioned_ensembl_gene_id":"ENSG00000176358.15","gene_symbol":"TAC4","gene_name":"tachykinin 4 (hemokinin) [Source:HGNC Symbol;Acc:HGNC:16641]","synonyms":"Pptc,PPT-C,HK-1","biotype":"protein_coding","ncbi_id":"255061","summary":"This gene is a member of the tachykinin family of neurotransmitter-encoding genes. Tachykinin proteins are cleaved into small, secreted peptides that activate members of a family of receptor proteins. The products of this gene preferentially activate tachykinin receptor 1, and are thought to regulate peripheral endocrine and paracrine functions including blood pressure, the immune system, and endocrine gland secretion. The products of this gene lack a dibasic cleavage site found in other tachykinin proteins. Consequently, the nature of the cleavage products generated in vivo remains to be determined. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":49838309,"end":49848017,"strand":-1,"description":"tachykinin 4 (hemokinin) [Source:HGNC Symbol;Acc:HGNC:16641]"}, {"versioned_ensembl_gene_id":"ENSG00000226739.1","gene_symbol":"AL358972.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164346489,"end":164348644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165124.17","gene_symbol":"SVEP1","gene_name":"sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15985]","synonyms":"bA427L11.3,POLYDOM,FLJ13529,C9orf13","biotype":"protein_coding","ncbi_id":"79987","summary":null,"start":110365251,"end":110579880,"strand":-1,"description":"sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15985]"}, {"versioned_ensembl_gene_id":"ENSG00000260806.1","gene_symbol":"AL163051.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96500810,"end":96502321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157353.16","gene_symbol":"FUK","gene_name":"fucokinase [Source:HGNC Symbol;Acc:HGNC:29500]","synonyms":"FLJ39408","biotype":"protein_coding","ncbi_id":"197258","summary":"The protein encoded by this gene belongs to the GHMP (galacto-, homoserine, mevalonate and phosphomevalonate) kinase family and catalyzes the phosphorylation of L-fucose to form beta-L-fucose 1-phosphate. This enzyme catalyzes the first step in the utilization of free L-fucose in glycoprotein and glycolipid synthesis. L-fucose may be important in mediating a number of cell-cell interactions such as blood group antigen recognition, inflammation, and metastatis. While several transcript variants may exist for this gene, the full-length nature of only one has been described to date. [provided by RefSeq, Jul 2008]","start":70454421,"end":70480274,"strand":1,"description":"fucokinase [Source:HGNC Symbol;Acc:HGNC:29500]"}, {"versioned_ensembl_gene_id":"ENSG00000119285.10","gene_symbol":"HEATR1","gene_name":"HEAT repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:25517]","synonyms":"UTP10,FLJ10359,BAP28","biotype":"protein_coding","ncbi_id":"55127","summary":null,"start":236549005,"end":236604504,"strand":-1,"description":"HEAT repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:25517]"}, {"versioned_ensembl_gene_id":"ENSG00000242337.5","gene_symbol":"TFP1","gene_name":"transferrin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11759]","synonyms":"TFP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100129696","summary":null,"start":133661998,"end":133754576,"strand":1,"description":"transferrin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11759]"}, {"versioned_ensembl_gene_id":"ENSG00000253469.1","gene_symbol":"AC091819.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167164934,"end":167168401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247240.7","gene_symbol":"UBL7-AS1","gene_name":"UBL7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48614]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"440288","summary":null,"start":74461265,"end":74481302,"strand":1,"description":"UBL7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48614]"}, {"versioned_ensembl_gene_id":"ENSG00000142528.15","gene_symbol":"ZNF473","gene_name":"zinc finger protein 473 [Source:HGNC Symbol;Acc:HGNC:23239]","synonyms":"KIAA1141,HZFP100,DKFZP434N043","biotype":"protein_coding","ncbi_id":"25888","summary":"This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein, a component of the U7 snRNP complex, plays a role in histone 3'-end pre-mRNA processing and may be required for cell cycle progression to S phase. Expression level and methylation status of this gene may be correlated with bone mineral density. [provided by RefSeq, Jul 2016]","start":50025714,"end":50053414,"strand":1,"description":"zinc finger protein 473 [Source:HGNC Symbol;Acc:HGNC:23239]"}, {"versioned_ensembl_gene_id":"ENSG00000204282.4","gene_symbol":"TNRC6C-AS1","gene_name":"TNRC6C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44360]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100131096","summary":null,"start":78107398,"end":78111799,"strand":-1,"description":"TNRC6C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44360]"}, {"versioned_ensembl_gene_id":"ENSG00000249073.1","gene_symbol":"WSPAR","gene_name":"WNT signaling pathway activating non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51639]","synonyms":"lncTCF7,TCONS_00009511-XLOC_004555","biotype":"lincRNA","ncbi_id":"105664404","summary":null,"start":133913677,"end":133917269,"strand":1,"description":"WNT signaling pathway activating non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51639]"}, {"versioned_ensembl_gene_id":"ENSG00000216588.8","gene_symbol":"IGSF23","gene_name":"immunoglobulin superfamily member 23 [Source:HGNC Symbol;Acc:HGNC:40040]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147710","summary":"This gene encodes a protein that has one immunoglobulin (Ig) domain and is a member of the immunoglobulin superfamily. Proteins in this superfamily are usually found on or in cell membranes and act as receptors in immune response pathways. [provided by RefSeq, Nov 2011]","start":44613630,"end":44636781,"strand":1,"description":"immunoglobulin superfamily member 23 [Source:HGNC Symbol;Acc:HGNC:40040]"}, {"versioned_ensembl_gene_id":"ENSG00000152818.18","gene_symbol":"UTRN","gene_name":"utrophin [Source:HGNC Symbol;Acc:HGNC:12635]","synonyms":"DRP1,DRP,DMDL","biotype":"protein_coding","ncbi_id":"7402","summary":"This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]","start":144285701,"end":144853034,"strand":1,"description":"utrophin [Source:HGNC Symbol;Acc:HGNC:12635]"}, {"versioned_ensembl_gene_id":"ENSG00000070367.15","gene_symbol":"EXOC5","gene_name":"exocyst complex component 5 [Source:HGNC Symbol;Acc:HGNC:10696]","synonyms":"SEC10,SEC10P,SEC10L1","biotype":"protein_coding","ncbi_id":"10640","summary":"The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. [provided by RefSeq, Jul 2008]","start":57200507,"end":57269008,"strand":-1,"description":"exocyst complex component 5 [Source:HGNC Symbol;Acc:HGNC:10696]"}, {"versioned_ensembl_gene_id":"ENSG00000276846.1","gene_symbol":"AC016590.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37314868,"end":37315620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223953.5","gene_symbol":"C1QTNF5","gene_name":"C1q and TNF related 5 [Source:HGNC Symbol;Acc:HGNC:14344]","synonyms":"LORD,DKFZp586B0621,CTRP5","biotype":"protein_coding","ncbi_id":"114902","summary":"This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled-related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter. [provided by RefSeq, Jun 2013]","start":119338939,"end":119340940,"strand":-1,"description":"C1q and TNF related 5 [Source:HGNC Symbol;Acc:HGNC:14344]"}, {"versioned_ensembl_gene_id":"ENSG00000248844.6","gene_symbol":"AP003555.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70056230,"end":70065371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251243.1","gene_symbol":"AC005178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133720495,"end":133720934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225623.1","gene_symbol":"AGBL4-IT1","gene_name":"AGBL4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41482]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874313","summary":null,"start":49374201,"end":49472085,"strand":-1,"description":"AGBL4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41482]"}, {"versioned_ensembl_gene_id":"ENSG00000233941.1","gene_symbol":"AL356859.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106358566,"end":106359717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216352.1","gene_symbol":"AL590824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80555841,"end":80557189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236775.1","gene_symbol":"AL512637.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":247015068,"end":247017291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213539.4","gene_symbol":"YBX1P6","gene_name":"Y-box binding protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42427]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402375","summary":null,"start":109532830,"end":109534332,"strand":-1,"description":"Y-box binding protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42427]"}, {"versioned_ensembl_gene_id":"ENSG00000110092.3","gene_symbol":"CCND1","gene_name":"cyclin D1 [Source:HGNC Symbol;Acc:HGNC:1582]","synonyms":"U21B31,PRAD1,D11S287E,BCL1","biotype":"protein_coding","ncbi_id":"595","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance throughout the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK4 or CDK6, whose activity is required for cell cycle G1/S transition. This protein has been shown to interact with tumor suppressor protein Rb and the expression of this gene is regulated positively by Rb. Mutations, amplification and overexpression of this gene, which alters cell cycle progression, are observed frequently in a variety of human cancers. [provided by RefSeq, Dec 2019]","start":69641087,"end":69654474,"strand":1,"description":"cyclin D1 [Source:HGNC Symbol;Acc:HGNC:1582]"}, {"versioned_ensembl_gene_id":"ENSG00000274486.1","gene_symbol":"AP002383.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95030549,"end":95031245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249484.8","gene_symbol":"LINC01470","gene_name":"long intergenic non-protein coding RNA 1470 [Source:HGNC Symbol;Acc:HGNC:51105]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927134","summary":null,"start":152618965,"end":153223543,"strand":-1,"description":"long intergenic non-protein coding RNA 1470 [Source:HGNC Symbol;Acc:HGNC:51105]"}, {"versioned_ensembl_gene_id":"ENSG00000100744.14","gene_symbol":"GSKIP","gene_name":"GSK3B interacting protein [Source:HGNC Symbol;Acc:HGNC:20343]","synonyms":"C14orf129","biotype":"protein_coding","ncbi_id":"51527","summary":"This gene encodes a protein that is involved as a negative regulator of GSK3-beta in the Wnt signaling pathway. The encoded protein may play a role in the retinoic acid signaling pathway by regulating the functional interactions between GSK3-beta, beta-catenin and cyclin D1, and it regulates the beta-catenin/N-cadherin pool. The encoded protein contains a GSK3-beta interacting domain (GID) in its C-terminus, which is similar to the GID of Axin. The protein also contains an evolutionarily conserved RII-binding domain, which facilitates binding with protein kinase-A and GSK3-beta, enabling its role as an A-kinase anchoring protein. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2012]","start":96363452,"end":96387288,"strand":1,"description":"GSK3B interacting protein [Source:HGNC Symbol;Acc:HGNC:20343]"}, {"versioned_ensembl_gene_id":"ENSG00000234675.1","gene_symbol":"AL445123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148017422,"end":148020974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228222.1","gene_symbol":"AC073050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167293171,"end":167558333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258566.2","gene_symbol":"AC007376.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76690139,"end":76690742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127804.12","gene_symbol":"METTL16","gene_name":"methyltransferase like 16 [Source:HGNC Symbol;Acc:HGNC:28484]","synonyms":"MGC3329,METT10D","biotype":"protein_coding","ncbi_id":"79066","summary":null,"start":2405562,"end":2511891,"strand":-1,"description":"methyltransferase like 16 [Source:HGNC Symbol;Acc:HGNC:28484]"}, {"versioned_ensembl_gene_id":"ENSG00000182197.10","gene_symbol":"EXT1","gene_name":"exostosin glycosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3512]","synonyms":"ttv,LGS,LGCR","biotype":"protein_coding","ncbi_id":"2131","summary":"This gene encodes an endoplasmic reticulum-resident type II transmembrane glycosyltransferase involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type I form of multiple exostoses. [provided by RefSeq, Jul 2008]","start":117794490,"end":118111853,"strand":-1,"description":"exostosin glycosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3512]"}, {"versioned_ensembl_gene_id":"ENSG00000250300.1","gene_symbol":"AP001960.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99469598,"end":99498698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250983.1","gene_symbol":"AC022296.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133546071,"end":133546272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152611.11","gene_symbol":"CAPSL","gene_name":"calcyphosine like [Source:HGNC Symbol;Acc:HGNC:28375]","synonyms":"MGC26610","biotype":"protein_coding","ncbi_id":"133690","summary":null,"start":35904295,"end":35938779,"strand":-1,"description":"calcyphosine like [Source:HGNC Symbol;Acc:HGNC:28375]"}, {"versioned_ensembl_gene_id":"ENSG00000267065.2","gene_symbol":"LINC02080","gene_name":"long intergenic non-protein coding RNA 2080 [Source:HGNC Symbol;Acc:HGNC:52928]","synonyms":"FLJ30938","biotype":"lincRNA","ncbi_id":"101928514","summary":null,"start":76799044,"end":76807102,"strand":1,"description":"long intergenic non-protein coding RNA 2080 [Source:HGNC Symbol;Acc:HGNC:52928]"}, {"versioned_ensembl_gene_id":"ENSG00000259719.5","gene_symbol":"LINC02284","gene_name":"long intergenic non-protein coding RNA 2284 [Source:HGNC Symbol;Acc:HGNC:53201]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723699","summary":null,"start":56310880,"end":56345001,"strand":1,"description":"long intergenic non-protein coding RNA 2284 [Source:HGNC Symbol;Acc:HGNC:53201]"}, {"versioned_ensembl_gene_id":"ENSG00000183578.6","gene_symbol":"TNFAIP8L3","gene_name":"TNF alpha induced protein 8 like 3 [Source:HGNC Symbol;Acc:HGNC:20620]","synonyms":"FLJ41287","biotype":"protein_coding","ncbi_id":"388121","summary":null,"start":51056598,"end":51105276,"strand":-1,"description":"TNF alpha induced protein 8 like 3 [Source:HGNC Symbol;Acc:HGNC:20620]"}, {"versioned_ensembl_gene_id":"ENSG00000214626.2","gene_symbol":"POLR3DP1","gene_name":"RNA polymerase III subunit D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422384","summary":null,"start":74654956,"end":74656131,"strand":1,"description":"RNA polymerase III subunit D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45107]"}, {"versioned_ensembl_gene_id":"ENSG00000213731.2","gene_symbol":"RAB5CP1","gene_name":"RAB5C, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45104]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420734","summary":null,"start":74423435,"end":74424014,"strand":-1,"description":"RAB5C, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45104]"}, {"versioned_ensembl_gene_id":"ENSG00000233904.6","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30479321,"end":30484059,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000249966.1","gene_symbol":"AC025183.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1850950,"end":1851497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232342.7","gene_symbol":"AC022540.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74506081,"end":74530553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183011.13","gene_symbol":"NAA38","gene_name":"N(alpha)-acetyltransferase 38, NatC auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:28212]","synonyms":"PFAAP2,MGC14151,LSMD1","biotype":"protein_coding","ncbi_id":"84316","summary":null,"start":7856685,"end":7885238,"strand":-1,"description":"N(alpha)-acetyltransferase 38, NatC auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:28212]"}, {"versioned_ensembl_gene_id":"ENSG00000142405.21","gene_symbol":"NLRP12","gene_name":"NLR family pyrin domain containing 12 [Source:HGNC Symbol;Acc:HGNC:22938]","synonyms":"PYPAF7,PAN6,NALP12,Monarch1,CLR19.3,RNO2","biotype":"protein_coding","ncbi_id":"91662","summary":"This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":53793603,"end":53824394,"strand":-1,"description":"NLR family pyrin domain containing 12 [Source:HGNC Symbol;Acc:HGNC:22938]"}, {"versioned_ensembl_gene_id":"ENSG00000263206.1","gene_symbol":"KYNUP3","gene_name":"kynureninase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39201]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729323","summary":null,"start":19208584,"end":19211359,"strand":1,"description":"kynureninase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39201]"}, {"versioned_ensembl_gene_id":"ENSG00000258454.1","gene_symbol":"AC016526.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":76235817,"end":76263474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255666.5","gene_symbol":"AP000943.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94641907,"end":94651631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177807.8","gene_symbol":"KCNJ10","gene_name":"potassium voltage-gated channel subfamily J member 10 [Source:HGNC Symbol;Acc:HGNC:6256]","synonyms":"Kir4.1,Kir1.2","biotype":"protein_coding","ncbi_id":"3766","summary":"This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. [provided by RefSeq, Jul 2008]","start":159998651,"end":160070483,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 10 [Source:HGNC Symbol;Acc:HGNC:6256]"}, {"versioned_ensembl_gene_id":"ENSG00000255135.3","gene_symbol":"AP002360.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76441338,"end":76444656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253635.1","gene_symbol":"IGHVIII-67-3","gene_name":"immunoglobulin heavy variable (III)-67-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5706]","synonyms":"IGHV(III)-67-3","biotype":"IG_V_pseudogene","ncbi_id":"28341","summary":null,"start":106692657,"end":106692888,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5706]"}, {"versioned_ensembl_gene_id":"ENSG00000269608.1","gene_symbol":"AC011487.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53616802,"end":53617254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176244.6","gene_symbol":"ACBD7","gene_name":"acyl-CoA binding domain containing 7 [Source:HGNC Symbol;Acc:HGNC:17715]","synonyms":"FLJ38219,bA455B2.2","biotype":"protein_coding","ncbi_id":"414149","summary":null,"start":15077523,"end":15088776,"strand":-1,"description":"acyl-CoA binding domain containing 7 [Source:HGNC Symbol;Acc:HGNC:17715]"}, {"versioned_ensembl_gene_id":"ENSG00000152492.13","gene_symbol":"CCDC50","gene_name":"coiled-coil domain containing 50 [Source:HGNC Symbol;Acc:HGNC:18111]","synonyms":"Ymer,DFNA44,C3orf6","biotype":"protein_coding","ncbi_id":"152137","summary":"This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":191329077,"end":191398670,"strand":1,"description":"coiled-coil domain containing 50 [Source:HGNC Symbol;Acc:HGNC:18111]"}, {"versioned_ensembl_gene_id":"ENSG00000163904.12","gene_symbol":"SENP2","gene_name":"SUMO1/sentrin/SMT3 specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:23116]","synonyms":"SMT3IP2,KIAA1331,DKFZp762A2316,AXAM2","biotype":"protein_coding","ncbi_id":"59343","summary":"SUMO1 (UBL1; MIM 601912) is a small ubiquitin-like protein that can be covalently conjugated to other proteins. SENP2 is one of a group of enzymes that process newly synthesized SUMO1 into the conjugatable form and catalyze the deconjugation of SUMO1-containing species.[supplied by OMIM, Apr 2004]","start":185582496,"end":185633551,"strand":1,"description":"SUMO1/sentrin/SMT3 specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:23116]"}, {"versioned_ensembl_gene_id":"ENSG00000273502.4","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724478,"end":54736594,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000165119.20","gene_symbol":"HNRNPK","gene_name":"heterogeneous nuclear ribonucleoprotein K [Source:HGNC Symbol;Acc:HGNC:5044]","synonyms":"TUNP,HNRPK,CSBP","biotype":"protein_coding","ncbi_id":"3190","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene is located in the nucleoplasm and has three repeats of KH domains that binds to RNAs. It is distinct among other hnRNP proteins in its binding preference; it binds tenaciously to poly(C). This protein is also thought to have a role during cell cycle progession. Several alternatively spliced transcript variants have been described for this gene, however, not all of them are fully characterized. [provided by RefSeq, Jul 2008]","start":83968083,"end":83980616,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein K [Source:HGNC Symbol;Acc:HGNC:5044]"}, {"versioned_ensembl_gene_id":"ENSG00000260230.2","gene_symbol":"FRRS1L","gene_name":"ferric chelate reductase 1 like [Source:HGNC Symbol;Acc:HGNC:1362]","synonyms":"CG-6,C9orf4","biotype":"protein_coding","ncbi_id":"23732","summary":"This gene encodes a component of the outer-core of an alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor protein in the brain. The encoded protein is thought to interact with inner-core components of the receptor, and play a role in the modulation of glutamate signaling. Mutations in this gene are associated with early infantile epileptic encephalopathy 37. [provided by RefSeq, Jul 2016]","start":109130293,"end":109167291,"strand":-1,"description":"ferric chelate reductase 1 like [Source:HGNC Symbol;Acc:HGNC:1362]"}, {"versioned_ensembl_gene_id":"ENSG00000272301.1","gene_symbol":"AP002360.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76389648,"end":76390128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260051.1","gene_symbol":"AL031600.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1451760,"end":1452653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266664.1","gene_symbol":"AC007952.9","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19150279,"end":19151286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255368.1","gene_symbol":"AC087373.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25140533,"end":25141023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095261.13","gene_symbol":"PSMD5","gene_name":"proteasome 26S subunit, non-ATPase 5 [Source:HGNC Symbol;Acc:HGNC:9563]","synonyms":"S5B,KIAA0072","biotype":"protein_coding","ncbi_id":"5711","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a non-ATPase subunit of the 19S regulator base that functions as a chaperone protein during 26S proteasome assembly. [provided by RefSeq, Jul 2012]","start":120815496,"end":120842984,"strand":-1,"description":"proteasome 26S subunit, non-ATPase 5 [Source:HGNC Symbol;Acc:HGNC:9563]"}, {"versioned_ensembl_gene_id":"ENSG00000231502.6","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"G7b,C6orf28,YBL026W","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31779577,"end":31789166,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000268883.2","gene_symbol":"PNMA6B","gene_name":"paraneoplastic Ma antigen family member 6B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26681]","synonyms":"PNMA6D","biotype":"unprocessed_pseudogene","ncbi_id":"728513","summary":null,"start":153075769,"end":153076968,"strand":-1,"description":"paraneoplastic Ma antigen family member 6B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26681]"}, {"versioned_ensembl_gene_id":"ENSG00000161542.16","gene_symbol":"PRPSAP1","gene_name":"phosphoribosyl pyrophosphate synthetase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:9466]","synonyms":"PAP39","biotype":"protein_coding","ncbi_id":"5635","summary":null,"start":76309486,"end":76384521,"strand":-1,"description":"phosphoribosyl pyrophosphate synthetase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:9466]"}, {"versioned_ensembl_gene_id":"ENSG00000160472.4","gene_symbol":"TMEM190","gene_name":"transmembrane protein 190 [Source:HGNC Symbol;Acc:HGNC:29632]","synonyms":"MDAC1","biotype":"protein_coding","ncbi_id":"147744","summary":null,"start":55376836,"end":55378244,"strand":1,"description":"transmembrane protein 190 [Source:HGNC Symbol;Acc:HGNC:29632]"}, {"versioned_ensembl_gene_id":"ENSG00000214654.7","gene_symbol":"AL161911.1","gene_name":"Putative UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase LOC100288842 [Source:UniProtKB/Swiss-Prot;Acc:A8MXE2]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":120793551,"end":120799918,"strand":1,"description":"Putative UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase LOC100288842 [Source:UniProtKB/Swiss-Prot;Acc:A8MXE2]"}, {"versioned_ensembl_gene_id":"ENSG00000230197.6","gene_symbol":"AC007952.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19077775,"end":19087878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129646.14","gene_symbol":"QRICH2","gene_name":"glutamine rich 2 [Source:HGNC Symbol;Acc:HGNC:25326]","synonyms":"DKFZP434P0316","biotype":"protein_coding","ncbi_id":"84074","summary":null,"start":76274049,"end":76307998,"strand":-1,"description":"glutamine rich 2 [Source:HGNC Symbol;Acc:HGNC:25326]"}, {"versioned_ensembl_gene_id":"ENSG00000262074.6","gene_symbol":"SNORD3B-2","gene_name":"small nucleolar RNA, C/D box 3B-2 [Source:HGNC Symbol;Acc:HGNC:33190]","synonyms":"U3b2,U3-2B","biotype":"snoRNA","ncbi_id":"780852","summary":null,"start":19063346,"end":19064136,"strand":-1,"description":"small nucleolar RNA, C/D box 3B-2 [Source:HGNC Symbol;Acc:HGNC:33190]"}, {"versioned_ensembl_gene_id":"ENSG00000233376.1","gene_symbol":"AL117382.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44389624,"end":44391537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229920.2","gene_symbol":"RPS4XP5","gene_name":"ribosomal protein S4X pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36670]","synonyms":"RPS4P5","biotype":"transcribed_processed_pseudogene","ncbi_id":"100271132","summary":null,"start":63642455,"end":63644038,"strand":-1,"description":"ribosomal protein S4X pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36670]"}, {"versioned_ensembl_gene_id":"ENSG00000223648.4","gene_symbol":"IGHV3-64","gene_name":"immunoglobulin heavy variable 3-64 [Source:HGNC Symbol;Acc:HGNC:5617]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28414","summary":null,"start":106657725,"end":106658258,"strand":-1,"description":"immunoglobulin heavy variable 3-64 [Source:HGNC Symbol;Acc:HGNC:5617]"}, {"versioned_ensembl_gene_id":"ENSG00000267881.1","gene_symbol":"AC243967.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41708612,"end":41761282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234340.1","gene_symbol":"AP000705.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22134698,"end":22136083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229221.1","gene_symbol":"HNRNPA1P66","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48796]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391378","summary":null,"start":63751697,"end":63752630,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:48796]"}, {"versioned_ensembl_gene_id":"ENSG00000217557.1","gene_symbol":"AL590286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":162957258,"end":162957548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172367.15","gene_symbol":"PDZD3","gene_name":"PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19891]","synonyms":"IKEPP,FLJ22756,PDZK2","biotype":"protein_coding","ncbi_id":"79849","summary":"Guanylyl cyclase C (GCC, or GUCY2C; MIM 601330) produces cGMP following the binding of either endogenous ligands or heat-stable enterotoxins secreted by E. coli and other enteric bacteria. Activation of GCC initiates a signaling cascade that leads to phosphorylation of the cystic fibrosis transmembrane conductance regulator (CFTR; MIM 602421), followed by a net efflux of ions and water into the intestinal lumen. IKEPP is a regulatory protein that associates with GCC and regulates the amount of cGMP produced following receptor stimulation (Scott et al., 2002 [PubMed 11950846]).[supplied by OMIM, Mar 2008]","start":119185457,"end":119190223,"strand":1,"description":"PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19891]"}, {"versioned_ensembl_gene_id":"ENSG00000180043.11","gene_symbol":"FAM71E2","gene_name":"family with sequence similarity 71 member E2 [Source:HGNC Symbol;Acc:HGNC:25278]","synonyms":"DKFZp434G1729,C19orf16","biotype":"protein_coding","ncbi_id":"284418","summary":null,"start":55354908,"end":55363260,"strand":-1,"description":"family with sequence similarity 71 member E2 [Source:HGNC Symbol;Acc:HGNC:25278]"}, {"versioned_ensembl_gene_id":"ENSG00000224496.7","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30128631,"end":30141238,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000253862.1","gene_symbol":"IGHVIII-47-1","gene_name":"immunoglobulin heavy variable (III)-47-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5701]","synonyms":"IGHV(III)-47-1","biotype":"IG_V_pseudogene","ncbi_id":"28344","summary":null,"start":106531141,"end":106531471,"strand":-1,"description":"immunoglobulin heavy variable (III)-47-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5701]"}, {"versioned_ensembl_gene_id":"ENSG00000259378.1","gene_symbol":"DCAF13P3","gene_name":"DDB1 and CUL4 associated factor 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43868]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132724","summary":null,"start":50944663,"end":50945996,"strand":1,"description":"DDB1 and CUL4 associated factor 13 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43868]"}, {"versioned_ensembl_gene_id":"ENSG00000007306.14","gene_symbol":"CEACAM7","gene_name":"carcinoembryonic antigen related cell adhesion molecule 7 [Source:HGNC Symbol;Acc:HGNC:1819]","synonyms":"CGM2,CEA","biotype":"protein_coding","ncbi_id":"1087","summary":"This gene encodes a cell surface glycoprotein and member of the carcinoembryonic antigen (CEA) family of proteins. Expression of this gene may be downregulated in colon and rectal cancer. Additionally, lower expression levels of this gene may be predictive of rectal cancer recurrence. This gene is present in a CEA family gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":41673307,"end":41706976,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 7 [Source:HGNC Symbol;Acc:HGNC:1819]"}, {"versioned_ensembl_gene_id":"ENSG00000183908.5","gene_symbol":"LRRC55","gene_name":"leucine rich repeat containing 55 [Source:HGNC Symbol;Acc:HGNC:32324]","synonyms":"FLJ45686","biotype":"protein_coding","ncbi_id":"219527","summary":null,"start":57181747,"end":57191717,"strand":1,"description":"leucine rich repeat containing 55 [Source:HGNC Symbol;Acc:HGNC:32324]"}, {"versioned_ensembl_gene_id":"ENSG00000255489.1","gene_symbol":"AC115990.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24701275,"end":24701575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085999.11","gene_symbol":"RAD54L","gene_name":"RAD54 like (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:9826]","synonyms":"RAD54A,hRAD54,hHR54","biotype":"protein_coding","ncbi_id":"8438","summary":"The protein encoded by this gene belongs to the DEAD-like helicase superfamily, and shares similarity with Saccharomyces cerevisiae Rad54, a protein known to be involved in the homologous recombination and repair of DNA. This protein has been shown to play a role in homologous recombination related repair of DNA double-strand breaks. The binding of this protein to double-strand DNA induces a DNA topological change, which is thought to facilitate homologous DNA paring, and stimulate DNA recombination. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Dec 2008]","start":46247688,"end":46278473,"strand":1,"description":"RAD54 like (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:9826]"}, {"versioned_ensembl_gene_id":"ENSG00000259104.2","gene_symbol":"PTCSC3","gene_name":"papillary thyroid carcinoma susceptibility candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43959]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100886964","summary":null,"start":36136108,"end":36176468,"strand":-1,"description":"papillary thyroid carcinoma susceptibility candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43959]"}, {"versioned_ensembl_gene_id":"ENSG00000140807.6","gene_symbol":"NKD1","gene_name":"naked cuticle homolog 1 [Source:HGNC Symbol;Acc:HGNC:17045]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85407","summary":"In the mouse, Nkd is a Dishevelled (see DVL1; MIM 601365)-binding protein that functions as a negative regulator of the Wnt (see WNT1; MIM 164820)-beta-catenin (see MIM 116806)-Tcf (see MIM 602272) signaling pathway.[supplied by OMIM, Jun 2003]","start":50548330,"end":50649249,"strand":1,"description":"naked cuticle homolog 1 [Source:HGNC Symbol;Acc:HGNC:17045]"}, {"versioned_ensembl_gene_id":"ENSG00000111799.20","gene_symbol":"COL12A1","gene_name":"collagen type XII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2188]","synonyms":"COL12A1L","biotype":"protein_coding","ncbi_id":"1303","summary":"This gene encodes the alpha chain of type XII collagen, a member of the FACIT (fibril-associated collagens with interrupted triple helices) collagen family. Type XII collagen is a homotrimer found in association with type I collagen, an association that is thought to modify the interactions between collagen I fibrils and the surrounding matrix. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":75084326,"end":75206051,"strand":-1,"description":"collagen type XII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2188]"}, {"versioned_ensembl_gene_id":"ENSG00000175984.14","gene_symbol":"DENND2C","gene_name":"DENN domain containing 2C [Source:HGNC Symbol;Acc:HGNC:24748]","synonyms":"RP5-1156J9.1,FLJ37099,DKFZp779P1149,DKFZp686G0351,dJ1156J9.1","biotype":"protein_coding","ncbi_id":"163259","summary":null,"start":114582848,"end":114670422,"strand":-1,"description":"DENN domain containing 2C [Source:HGNC Symbol;Acc:HGNC:24748]"}, {"versioned_ensembl_gene_id":"ENSG00000270751.1","gene_symbol":"FBXW7-AS1","gene_name":"FBXW7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52397]","synonyms":"DEspR,DEAR","biotype":"antisense_RNA","ncbi_id":"102191832","summary":null,"start":152337655,"end":152338098,"strand":1,"description":"FBXW7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52397]"}, {"versioned_ensembl_gene_id":"ENSG00000255893.1","gene_symbol":"AP000786.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94472908,"end":94473570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171204.12","gene_symbol":"TMEM126B","gene_name":"transmembrane protein 126B [Source:HGNC Symbol;Acc:HGNC:30883]","synonyms":"HT007","biotype":"protein_coding","ncbi_id":"55863","summary":"This gene encodes a mitochondrial transmembrane protein which is a component of the mitochondrial complex I assembly complex. The encoded protein serves as an assembly factor that is required for formation of the membrane arm of the complex. It interacts with NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 13. Naturally occurring mutations in this gene are associated with isolated complex I deficiency. A pseudogene of this gene has been defined on chromosome 9. [provided by RefSeq, Apr 2017]","start":85628573,"end":85636539,"strand":1,"description":"transmembrane protein 126B [Source:HGNC Symbol;Acc:HGNC:30883]"}, {"versioned_ensembl_gene_id":"ENSG00000250062.5","gene_symbol":"AC104827.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86117912,"end":86219926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224668.1","gene_symbol":"IPO8P1","gene_name":"importin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41955]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418819","summary":null,"start":210859177,"end":210862285,"strand":-1,"description":"importin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41955]"}, {"versioned_ensembl_gene_id":"ENSG00000284376.1","gene_symbol":"AC092017.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":211108445,"end":211207138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223814.1","gene_symbol":"AL691459.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47761132,"end":47765547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257384.1","gene_symbol":"AC009779.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55732366,"end":55732648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271303.1","gene_symbol":"SRXN1","gene_name":"sulfiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:16132]","synonyms":"SRX1,Npn3,dJ850E9.2,C20orf139,YKL086W","biotype":"protein_coding","ncbi_id":"140809","summary":null,"start":646615,"end":653370,"strand":-1,"description":"sulfiredoxin 1 [Source:HGNC Symbol;Acc:HGNC:16132]"}, {"versioned_ensembl_gene_id":"ENSG00000248144.5","gene_symbol":"ADH1C","gene_name":"alcohol dehydrogenase 1C (class I), gamma polypeptide [Source:HGNC Symbol;Acc:HGNC:251]","synonyms":"ADH3","biotype":"protein_coding","ncbi_id":"126","summary":"This gene encodes class I alcohol dehydrogenase, gamma subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class I alcohol dehydrogenase, consisting of several homo- and heterodimers of alpha, beta, and gamma subunits, exhibits high activity for ethanol oxidation to acetaldehyde, thus playing a major role in ethanol catabolism. Three genes encoding alpha, beta and gamma subunits are tandemly organized in a genomic segment as a gene cluster. An association between ADH1C polymorphism and alcohol dependence has not been established. [provided by RefSeq, Sep 2019]","start":99336492,"end":99353027,"strand":-1,"description":"alcohol dehydrogenase 1C (class I), gamma polypeptide [Source:HGNC Symbol;Acc:HGNC:251]"}, {"versioned_ensembl_gene_id":"ENSG00000229554.2","gene_symbol":"RPL21P24","gene_name":"ribosomal protein L21 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35702]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270880","summary":null,"start":47497894,"end":47498341,"strand":-1,"description":"ribosomal protein L21 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35702]"}, {"versioned_ensembl_gene_id":"ENSG00000244130.1","gene_symbol":"UBE2Q2P9","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49517]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480276","summary":null,"start":72006774,"end":72006975,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49517]"}, {"versioned_ensembl_gene_id":"ENSG00000271355.1","gene_symbol":"AL356458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47483698,"end":47484162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276395.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832694,"end":54847510,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000165061.14","gene_symbol":"ZMAT4","gene_name":"zinc finger matrin-type 4 [Source:HGNC Symbol;Acc:HGNC:25844]","synonyms":"FLJ13842","biotype":"protein_coding","ncbi_id":"79698","summary":null,"start":40530590,"end":40897833,"strand":-1,"description":"zinc finger matrin-type 4 [Source:HGNC Symbol;Acc:HGNC:25844]"}, {"versioned_ensembl_gene_id":"ENSG00000250506.7","gene_symbol":"CDK3","gene_name":"cyclin dependent kinase 3 [Source:HGNC Symbol;Acc:HGNC:1772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1018","summary":"This gene encodes a member of the cyclin-dependent protein kinase family. The protein promotes entry into S phase, in part by activating members of the E2F family of transcription factors. The protein also associates with cyclin C and phosphorylates the retinoblastoma 1 protein to promote exit from G0. [provided by RefSeq, Jul 2008]","start":76000906,"end":76005999,"strand":1,"description":"cyclin dependent kinase 3 [Source:HGNC Symbol;Acc:HGNC:1772]"}, {"versioned_ensembl_gene_id":"ENSG00000253354.1","gene_symbol":"AC105999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40370028,"end":40401848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235623.2","gene_symbol":"OR7E110P","gene_name":"olfactory receptor family 7 subfamily E member 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:15126]","synonyms":"OR7E73P,OR7E72P,OR7E71P,OR7E68P,hg674,hg523,OR912-46,OR912-110,OR912-109,OR912-108,OR7E75P,OR7E74P","biotype":"unprocessed_pseudogene","ncbi_id":"81354","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14986942,"end":14987515,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:15126]"}, {"versioned_ensembl_gene_id":"ENSG00000088451.10","gene_symbol":"TGDS","gene_name":"TDP-glucose 4,6-dehydratase [Source:HGNC Symbol;Acc:HGNC:20324]","synonyms":"TDPGD,SDR2E1","biotype":"protein_coding","ncbi_id":"23483","summary":"The protein encoded by this gene is a member of the short-chain dehydrogenases/reductases (SDR) superfamily, and is thought to contain a nicotinamide adenine dinucleotide (NAD) binding domain. This large SDR family of enzymes is involved in the metabolism of a variety of compounds, including prostaglandins, retinoids, lipids, steroid hormones, and xenobiotics. Mutations in this gene have been associated with Catel-Manzke syndrome, which is characterized by Pierre Robin sequence, and radial deviation of the index finger due to the presence of an accessory bone between the index finger and its proximal phalanx. Pierre Robin sequence is defined by an undersized jaw, backwards displacement of the tongue base that causes an obstruction of the airways, and can also be associated with a cleft palate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":94574051,"end":94596257,"strand":-1,"description":"TDP-glucose 4,6-dehydratase [Source:HGNC Symbol;Acc:HGNC:20324]"}, {"versioned_ensembl_gene_id":"ENSG00000123901.8","gene_symbol":"GPR83","gene_name":"G protein-coupled receptor 83 [Source:HGNC Symbol;Acc:HGNC:4523]","synonyms":"GPR72","biotype":"protein_coding","ncbi_id":"10888","summary":null,"start":94377311,"end":94401419,"strand":-1,"description":"G protein-coupled receptor 83 [Source:HGNC Symbol;Acc:HGNC:4523]"}, {"versioned_ensembl_gene_id":"ENSG00000182013.17","gene_symbol":"PNMA8A","gene_name":"paraneoplastic Ma antigen family member 8A [Source:HGNC Symbol;Acc:HGNC:25578]","synonyms":"PNMAL1,KIAA1183L,FLJ10781","biotype":"protein_coding","ncbi_id":"55228","summary":null,"start":46466491,"end":46471563,"strand":-1,"description":"paraneoplastic Ma antigen family member 8A [Source:HGNC Symbol;Acc:HGNC:25578]"}, {"versioned_ensembl_gene_id":"ENSG00000231907.2","gene_symbol":"GAPDHP37","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:37791]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651258","summary":null,"start":40673484,"end":40674451,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:37791]"}, {"versioned_ensembl_gene_id":"ENSG00000219088.1","gene_symbol":"Z97206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105666326,"end":105667998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165959.11","gene_symbol":"CLMN","gene_name":"calmin [Source:HGNC Symbol;Acc:HGNC:19972]","synonyms":"KIAA1188,KIAA0500,FLJ12383","biotype":"protein_coding","ncbi_id":"79789","summary":null,"start":95181940,"end":95319906,"strand":-1,"description":"calmin [Source:HGNC Symbol;Acc:HGNC:19972]"}, {"versioned_ensembl_gene_id":"ENSG00000263002.7","gene_symbol":"ZNF234","gene_name":"zinc finger protein 234 [Source:HGNC Symbol;Acc:HGNC:13027]","synonyms":"ZNF269,HZF4","biotype":"protein_coding","ncbi_id":"10780","summary":null,"start":44141557,"end":44160309,"strand":1,"description":"zinc finger protein 234 [Source:HGNC Symbol;Acc:HGNC:13027]"}, {"versioned_ensembl_gene_id":"ENSG00000213020.9","gene_symbol":"ZNF611","gene_name":"zinc finger protein 611 [Source:HGNC Symbol;Acc:HGNC:28766]","synonyms":"MGC5384","biotype":"protein_coding","ncbi_id":"81856","summary":null,"start":52702813,"end":52735073,"strand":-1,"description":"zinc finger protein 611 [Source:HGNC Symbol;Acc:HGNC:28766]"}, {"versioned_ensembl_gene_id":"ENSG00000183914.14","gene_symbol":"DNAH2","gene_name":"dynein axonemal heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:2948]","synonyms":"KIAA1503,FLJ46675,DNHD3","biotype":"protein_coding","ncbi_id":"146754","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH2 is an axonemal inner arm dynein heavy chain (Chapelin et al., 1997 [PubMed 9256245]).[supplied by OMIM, Mar 2008]","start":7717354,"end":7833744,"strand":1,"description":"dynein axonemal heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:2948]"}, {"versioned_ensembl_gene_id":"ENSG00000219902.1","gene_symbol":"RPL35P3","gene_name":"ribosomal protein L35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35488]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728010","summary":null,"start":105302453,"end":105302823,"strand":-1,"description":"ribosomal protein L35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35488]"}, {"versioned_ensembl_gene_id":"ENSG00000267121.5","gene_symbol":"AC008105.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45190931,"end":45222222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261276.1","gene_symbol":"AP003071.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69004394,"end":69005100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204381.11","gene_symbol":"LAYN","gene_name":"layilin [Source:HGNC Symbol;Acc:HGNC:29471]","synonyms":"FLJ31092,FLJ30977","biotype":"protein_coding","ncbi_id":"143903","summary":null,"start":111540280,"end":111561745,"strand":1,"description":"layilin [Source:HGNC Symbol;Acc:HGNC:29471]"}, {"versioned_ensembl_gene_id":"ENSG00000261625.1","gene_symbol":"AP003071.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":69000765,"end":69002048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251249.1","gene_symbol":"AC097375.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":151955991,"end":151969381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275566.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54780466,"end":54797223,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000274707.5","gene_symbol":"GU182343.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54755098,"end":54764695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257614.1","gene_symbol":"AL133304.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35947556,"end":35950044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167130.17","gene_symbol":"DOLPP1","gene_name":"dolichyldiphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:29565]","synonyms":"LSFR2","biotype":"protein_coding","ncbi_id":"57171","summary":"A similar gene has been characterized in mice and encodes dolichyl pyrophosphate (Dol-P-P) phosphatase. This protein dephosphorylates dolichyl pyrophosphate so that it may be re-utilized as a glycosyl carrier lipid by the oligosaccharyltransferase multisubunit complex in the ER. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]","start":129081100,"end":129090438,"strand":1,"description":"dolichyldiphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:29565]"}, {"versioned_ensembl_gene_id":"ENSG00000092929.11","gene_symbol":"UNC13D","gene_name":"unc-13 homolog D [Source:HGNC Symbol;Acc:HGNC:23147]","synonyms":"Munc13-4","biotype":"protein_coding","ncbi_id":"201294","summary":"This gene encodes a protein that is a member of the UNC13 family, containing similar domain structure as other family members but lacking an N-terminal phorbol ester-binding C1 domain present in other Munc13 proteins. The protein appears to play a role in vesicle maturation during exocytosis and is involved in regulation of cytolytic granules secretion. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive disorder. [provided by RefSeq, Jul 2008]","start":75827225,"end":75844717,"strand":-1,"description":"unc-13 homolog D [Source:HGNC Symbol;Acc:HGNC:23147]"}, {"versioned_ensembl_gene_id":"ENSG00000266923.1","gene_symbol":"AC063949.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92421531,"end":92483680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224505.2","gene_symbol":"AC138150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45150400,"end":45161510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184343.10","gene_symbol":"SRPK3","gene_name":"SRSF protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:11402]","synonyms":"STK23,MSSK1","biotype":"protein_coding","ncbi_id":"26576","summary":"This gene encodes a protein kinase similar to a protein kinase which is specific for the SR (serine/arginine-rich domain) family of splicing factors. A highly similar protein has been shown to play a role in muscle development in mice. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":153776412,"end":153785732,"strand":1,"description":"SRSF protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:11402]"}, {"versioned_ensembl_gene_id":"ENSG00000132434.9","gene_symbol":"LANCL2","gene_name":"LanC like 2 [Source:HGNC Symbol;Acc:HGNC:6509]","synonyms":"TASP,GPR69B","biotype":"protein_coding","ncbi_id":"55915","summary":null,"start":55365448,"end":55433742,"strand":1,"description":"LanC like 2 [Source:HGNC Symbol;Acc:HGNC:6509]"}, {"versioned_ensembl_gene_id":"ENSG00000272886.5","gene_symbol":"DCP1A","gene_name":"decapping mRNA 1A [Source:HGNC Symbol;Acc:HGNC:18714]","synonyms":"HSA275986,SMIF,SMAD4IP1","biotype":"protein_coding","ncbi_id":"55802","summary":"Decapping is a key step in general and regulated mRNA decay. The protein encoded by this gene is a decapping enzyme. This protein and another decapping enzyme form a decapping complex, which interacts with the nonsense-mediated decay factor hUpf1 and may be recruited to mRNAs containing premature termination codons. This protein also participates in the TGF-beta signaling pathway. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":53283428,"end":53347610,"strand":-1,"description":"decapping mRNA 1A [Source:HGNC Symbol;Acc:HGNC:18714]"}, {"versioned_ensembl_gene_id":"ENSG00000214290.8","gene_symbol":"COLCA2","gene_name":"colorectal cancer associated 2 [Source:HGNC Symbol;Acc:HGNC:26978]","synonyms":"CASC13,C11orf93","biotype":"protein_coding","ncbi_id":"120376","summary":null,"start":111298555,"end":111308735,"strand":1,"description":"colorectal cancer associated 2 [Source:HGNC Symbol;Acc:HGNC:26978]"}, {"versioned_ensembl_gene_id":"ENSG00000211934.3","gene_symbol":"IGHV1-2","gene_name":"immunoglobulin heavy variable 1-2 [Source:HGNC Symbol;Acc:HGNC:5550]","synonyms":"V35","biotype":"IG_V_gene","ncbi_id":"28474","summary":null,"start":105986582,"end":105987083,"strand":-1,"description":"immunoglobulin heavy variable 1-2 [Source:HGNC Symbol;Acc:HGNC:5550]"}, {"versioned_ensembl_gene_id":"ENSG00000173744.17","gene_symbol":"AGFG1","gene_name":"ArfGAP with FG repeats 1 [Source:HGNC Symbol;Acc:HGNC:5175]","synonyms":"RIP,RAB,HRB","biotype":"protein_coding","ncbi_id":"3267","summary":"The protein encoded by this gene is related to nucleoporins, a class of proteins that mediate nucleocytoplasmic transport. The encoded protein binds the activation domain of the human immunodeficiency virus Rev protein when Rev is assembled onto its RNA target, and is required for the nuclear export of Rev-directed RNAs. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":227472152,"end":227561214,"strand":1,"description":"ArfGAP with FG repeats 1 [Source:HGNC Symbol;Acc:HGNC:5175]"}, {"versioned_ensembl_gene_id":"ENSG00000256705.3","gene_symbol":"AL137779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101833435,"end":101839531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023902.13","gene_symbol":"PLEKHO1","gene_name":"pleckstrin homology domain containing O1 [Source:HGNC Symbol;Acc:HGNC:24310]","synonyms":"OC120,CKIP-1","biotype":"protein_coding","ncbi_id":"51177","summary":null,"start":150149183,"end":150164720,"strand":1,"description":"pleckstrin homology domain containing O1 [Source:HGNC Symbol;Acc:HGNC:24310]"}, {"versioned_ensembl_gene_id":"ENSG00000187758.7","gene_symbol":"ADH1A","gene_name":"alcohol dehydrogenase 1A (class I), alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:249]","synonyms":"ADH1","biotype":"protein_coding","ncbi_id":"124","summary":"This gene encodes a member of the alcohol dehydrogenase family. The encoded protein is the alpha subunit of class I alcohol dehydrogenase, which consists of several homo- and heterodimers of alpha, beta and gamma subunits. Alcohol dehydrogenases catalyze the oxidation of alcohols to aldehydes. This gene is active in the liver in early fetal life but only weakly active in adult liver. This gene is found in a cluster with six additional alcohol dehydrogenase genes, including those encoding the beta and gamma subunits, on the long arm of chromosome 4. Mutations in this gene may contribute to variation in certain personality traits and substance dependence. [provided by RefSeq, Nov 2010]","start":99276367,"end":99291028,"strand":-1,"description":"alcohol dehydrogenase 1A (class I), alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:249]"}, {"versioned_ensembl_gene_id":"ENSG00000213556.3","gene_symbol":"AL359692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108836333,"end":108836597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249593.6","gene_symbol":"AC011405.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139012647,"end":139051203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259120.2","gene_symbol":"SMIM6","gene_name":"small integral membrane protein 6 [Source:HGNC Symbol;Acc:HGNC:40032]","synonyms":"C17orf110","biotype":"protein_coding","ncbi_id":"100130933","summary":null,"start":75646243,"end":75647977,"strand":1,"description":"small integral membrane protein 6 [Source:HGNC Symbol;Acc:HGNC:40032]"}, {"versioned_ensembl_gene_id":"ENSG00000102837.6","gene_symbol":"OLFM4","gene_name":"olfactomedin 4 [Source:HGNC Symbol;Acc:HGNC:17190]","synonyms":"GC1,OlfD,GW112","biotype":"protein_coding","ncbi_id":"10562","summary":"This gene was originally cloned from human myeloblasts and found to be selectively expressed in inflammed colonic epithelium. This gene encodes a member of the olfactomedin family. The encoded protein is an antiapoptotic factor that promotes tumor growth and is an extracellular matrix glycoprotein that facilitates cell adhesion. [provided by RefSeq, Mar 2011]","start":53028759,"end":53052057,"strand":1,"description":"olfactomedin 4 [Source:HGNC Symbol;Acc:HGNC:17190]"}, {"versioned_ensembl_gene_id":"ENSG00000267041.5","gene_symbol":"ZNF850","gene_name":"zinc finger protein 850 [Source:HGNC Symbol;Acc:HGNC:27994]","synonyms":"ZNF850P","biotype":"protein_coding","ncbi_id":"342892","summary":null,"start":36714383,"end":36772825,"strand":-1,"description":"zinc finger protein 850 [Source:HGNC Symbol;Acc:HGNC:27994]"}, {"versioned_ensembl_gene_id":"ENSG00000082269.16","gene_symbol":"FAM135A","gene_name":"family with sequence similarity 135 member A [Source:HGNC Symbol;Acc:HGNC:21084]","synonyms":"KIAA1411,FLJ20176","biotype":"protein_coding","ncbi_id":"57579","summary":null,"start":70412941,"end":70561174,"strand":1,"description":"family with sequence similarity 135 member A [Source:HGNC Symbol;Acc:HGNC:21084]"}, {"versioned_ensembl_gene_id":"ENSG00000115963.13","gene_symbol":"RND3","gene_name":"Rho family GTPase 3 [Source:HGNC Symbol;Acc:HGNC:671]","synonyms":"RhoE,Rho8,ARHE","biotype":"protein_coding","ncbi_id":"390","summary":"This gene encodes a protein which is a member of the small GTPase protein superfamily. The encoded protein binds only GTP but has no GTPase activity, and appears to act as a negative regulator of cytoskeletal organization leading to loss of adhesion. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011]","start":150468195,"end":150539011,"strand":-1,"description":"Rho family GTPase 3 [Source:HGNC Symbol;Acc:HGNC:671]"}, {"versioned_ensembl_gene_id":"ENSG00000232662.2","gene_symbol":"LDHBP1","gene_name":"lactate dehydrogenase B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6542]","synonyms":"LDHBL1","biotype":"processed_pseudogene","ncbi_id":"100289475","summary":null,"start":113276616,"end":113277734,"strand":1,"description":"lactate dehydrogenase B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6542]"}, {"versioned_ensembl_gene_id":"ENSG00000251547.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29417159,"end":29418105,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000148057.15","gene_symbol":"IDNK","gene_name":"IDNK, gluconokinase [Source:HGNC Symbol;Acc:HGNC:31367]","synonyms":"hGntK,C9orf103,bA522I20.2","biotype":"protein_coding","ncbi_id":"414328","summary":null,"start":83623049,"end":83644130,"strand":1,"description":"IDNK, gluconokinase [Source:HGNC Symbol;Acc:HGNC:31367]"}, {"versioned_ensembl_gene_id":"ENSG00000253435.1","gene_symbol":"IGKV2-4","gene_name":"immunoglobulin kappa variable 2-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5788]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28929","summary":null,"start":88931666,"end":88932380,"strand":-1,"description":"immunoglobulin kappa variable 2-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5788]"}, {"versioned_ensembl_gene_id":"ENSG00000133937.4","gene_symbol":"GSC","gene_name":"goosecoid homeobox [Source:HGNC Symbol;Acc:HGNC:4612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"145258","summary":"This gene encodes a member of the bicoid subfamily of the paired (PRD) homeobox family of proteins. The encoded protein acts as a transcription factor and may be autoregulatory. A similar protein in mice plays a role in craniofacial and rib cage development during embryogenesis. [provided by RefSeq, Jul 2008]","start":94768216,"end":94770230,"strand":-1,"description":"goosecoid homeobox [Source:HGNC Symbol;Acc:HGNC:4612]"}, {"versioned_ensembl_gene_id":"ENSG00000182712.15","gene_symbol":"CMC4","gene_name":"C-X9-C motif containing 4 [Source:HGNC Symbol;Acc:HGNC:35428]","synonyms":"P8MTCP1,p8,MTCP1NB,MTCP1","biotype":"protein_coding","ncbi_id":"100272147","summary":"This gene was identified by involvement in some t(X;14) translocations associated with mature T-cell proliferations. This region has a complex gene structure, with a common promoter and 5' exon spliced to two different sets of 3' exons that encode two different proteins. This gene represents the downstream 8 kDa protein that localizes to mitochondria.[provided by RefSeq, Mar 2009]","start":155061622,"end":155071362,"strand":-1,"description":"C-X9-C motif containing 4 [Source:HGNC Symbol;Acc:HGNC:35428]"}, {"versioned_ensembl_gene_id":"ENSG00000249996.1","gene_symbol":"AC106786.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123036271,"end":123054667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189419.6","gene_symbol":"SPATA41","gene_name":"spermatogenesis associated 41 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48613]","synonyms":"HSD47,FLJ42289","biotype":"lincRNA","ncbi_id":"388182","summary":null,"start":100344457,"end":100349655,"strand":-1,"description":"spermatogenesis associated 41 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48613]"}, {"versioned_ensembl_gene_id":"ENSG00000164299.6","gene_symbol":"SPZ1","gene_name":"spermatogenic leucine zipper 1 [Source:HGNC Symbol;Acc:HGNC:30721]","synonyms":"PPP1R148,NYD-TSP1,FLJ25709","biotype":"protein_coding","ncbi_id":"84654","summary":"This gene encodes a bHLH-zip transcription factor which functions in the mitogen-activate protein kinase (MAPK) signaling pathway. Because of its role in the upregulation of cell proliferation and tumorigenesis, this gene may serve as a target for Ras-induced tumor treatments. [provided by RefSeq, Oct 2011]","start":80319625,"end":80321842,"strand":1,"description":"spermatogenic leucine zipper 1 [Source:HGNC Symbol;Acc:HGNC:30721]"}, {"versioned_ensembl_gene_id":"ENSG00000213297.8","gene_symbol":"ZNF625-ZNF20","gene_name":"ZNF625-ZNF20 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48368]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529855","summary":"This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 625 (ZNF625) and zinc finger protein 20 (ZNF20) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":12132117,"end":12156731,"strand":-1,"description":"ZNF625-ZNF20 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48368]"}, {"versioned_ensembl_gene_id":"ENSG00000228205.1","gene_symbol":"AC131235.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184149704,"end":184150435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229315.6","gene_symbol":"MCHR2-AS1","gene_name":"MCHR2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48980]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"728012","summary":null,"start":99993944,"end":100076413,"strand":1,"description":"MCHR2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48980]"}, {"versioned_ensembl_gene_id":"ENSG00000102786.14","gene_symbol":"INTS6","gene_name":"integrator complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14879]","synonyms":"Notchl2,INT6,HDB,DICE1,DDX26A,DDX26,DBI-1","biotype":"protein_coding","ncbi_id":"26512","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. The protein encoded by this gene is a DEAD box protein that is part of a complex that interacts with the C-terminus of RNA polymerase II and is involved in 3' end processing of snRNAs. In addition, this gene is a candidate tumor suppressor and is located in the critical region of loss of heterozygosity (LOH). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2015]","start":51354077,"end":51454264,"strand":-1,"description":"integrator complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:14879]"}, {"versioned_ensembl_gene_id":"ENSG00000113532.12","gene_symbol":"ST8SIA4","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:10871]","synonyms":"SIAT8D,PST1,PST","biotype":"protein_coding","ncbi_id":"7903","summary":"The protein encoded by this gene catalyzes the polycondensation of alpha-2,8-linked sialic acid required for the synthesis of polysialic acid, a modulator of the adhesive properties of neural cell adhesion molecule (NCAM1). The encoded protein, which is a member of glycosyltransferase family 29, is a type II membrane protein that may be present in the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":100806935,"end":100903266,"strand":-1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:10871]"}, {"versioned_ensembl_gene_id":"ENSG00000260617.1","gene_symbol":"AC138028.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88741631,"end":88742367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278341.1","gene_symbol":"AC138028.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88708956,"end":88710437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154099.17","gene_symbol":"DNAAF1","gene_name":"dynein axonemal assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30539]","synonyms":"swt,ODA7,LRRC50,FLJ25330,CILD13","biotype":"protein_coding","ncbi_id":"123872","summary":"The protein encoded by this gene is cilium-specific and is required for the stability of the ciliary architecture. It is involved in the regulation of microtubule-based cilia and actin-based brush border microvilli. Mutations in this gene are associated with primary ciliary dyskinesia-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":84145287,"end":84178767,"strand":1,"description":"dynein axonemal assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:30539]"}, {"versioned_ensembl_gene_id":"ENSG00000166928.10","gene_symbol":"MS4A14","gene_name":"membrane spanning 4-domains A14 [Source:HGNC Symbol;Acc:HGNC:30706]","synonyms":"NYD-SP21,MS4A16,FLJ32856,DKFZp434H092","biotype":"protein_coding","ncbi_id":"84689","summary":null,"start":60378530,"end":60417756,"strand":1,"description":"membrane spanning 4-domains A14 [Source:HGNC Symbol;Acc:HGNC:30706]"}, {"versioned_ensembl_gene_id":"ENSG00000282067.1","gene_symbol":"MAPT-AS1","gene_name":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128977","summary":null,"start":45854974,"end":45907225,"strand":-1,"description":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]"}, {"versioned_ensembl_gene_id":"ENSG00000224999.1","gene_symbol":"VTA1P1","gene_name":"vesicle trafficking 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50483]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481708","summary":null,"start":169296471,"end":169297959,"strand":-1,"description":"vesicle trafficking 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50483]"}, {"versioned_ensembl_gene_id":"ENSG00000213859.4","gene_symbol":"KCTD11","gene_name":"potassium channel tetramerization domain containing 11 [Source:HGNC Symbol;Acc:HGNC:21302]","synonyms":"REN,KCASH1,C17orf36","biotype":"protein_coding","ncbi_id":"147040","summary":null,"start":7351889,"end":7354944,"strand":1,"description":"potassium channel tetramerization domain containing 11 [Source:HGNC Symbol;Acc:HGNC:21302]"}, {"versioned_ensembl_gene_id":"ENSG00000255196.1","gene_symbol":"OR4A17P","gene_name":"olfactory receptor family 4 subfamily A member 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:15154]","synonyms":"OR4A22P","biotype":"unprocessed_pseudogene","ncbi_id":"390139","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55444435,"end":55445338,"strand":1,"description":"olfactory receptor family 4 subfamily A member 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:15154]"}, {"versioned_ensembl_gene_id":"ENSG00000224888.4","gene_symbol":"AC138028.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88731180,"end":88741425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255444.1","gene_symbol":"CYCSP27","gene_name":"cytochrome c, somatic pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:24401]","synonyms":"HCP27","biotype":"processed_pseudogene","ncbi_id":"341148","summary":null,"start":74482250,"end":74482542,"strand":1,"description":"cytochrome c, somatic pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:24401]"}, {"versioned_ensembl_gene_id":"ENSG00000254631.5","gene_symbol":"AP001372.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74397549,"end":74485742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175591.11","gene_symbol":"P2RY2","gene_name":"purinergic receptor P2Y2 [Source:HGNC Symbol;Acc:HGNC:8541]","synonyms":"P2U","biotype":"protein_coding","ncbi_id":"5029","summary":"The product of this gene belongs to the family of P2 receptors, which is activated by extracellular nucleotides and subdivided into P2X ligand-gated ion channels and P2Y G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor, found on many cell types, is activated by ATP and UTP and is reported to be overexpressed on some cancer cell types. It is involved in many cellular functions, such as proliferation, apoptosis and inflammation. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Mar 2013]","start":73218298,"end":73236352,"strand":1,"description":"purinergic receptor P2Y2 [Source:HGNC Symbol;Acc:HGNC:8541]"}, {"versioned_ensembl_gene_id":"ENSG00000232186.1","gene_symbol":"AL137013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75326772,"end":75327999,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254358.1","gene_symbol":"CYCSP22","gene_name":"cytochrome c, somatic pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:24396]","synonyms":"HCP22","biotype":"processed_pseudogene","ncbi_id":"360175","summary":null,"start":50762460,"end":50762798,"strand":-1,"description":"cytochrome c, somatic pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:24396]"}, {"versioned_ensembl_gene_id":"ENSG00000232382.2","gene_symbol":"OR5K1","gene_name":"olfactory receptor family 5 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:8349]","synonyms":"HTPCRX10,HSHTPCRX10","biotype":"protein_coding","ncbi_id":"26339","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98463201,"end":98472924,"strand":1,"description":"olfactory receptor family 5 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:8349]"}, {"versioned_ensembl_gene_id":"ENSG00000105849.5","gene_symbol":"TWISTNB","gene_name":"TWIST neighbor [Source:HGNC Symbol;Acc:HGNC:18027]","synonyms":null,"biotype":"protein_coding","ncbi_id":"221830","summary":null,"start":19695462,"end":19709087,"strand":-1,"description":"TWIST neighbor [Source:HGNC Symbol;Acc:HGNC:18027]"}, {"versioned_ensembl_gene_id":"ENSG00000147853.16","gene_symbol":"AK3","gene_name":"adenylate kinase 3 [Source:HGNC Symbol;Acc:HGNC:17376]","synonyms":"AKL3L1,AK6,AK3L1","biotype":"protein_coding","ncbi_id":"50808","summary":"The protein encoded by this gene is a GTP:ATP phosphotransferase that is found in the mitochondrial matrix. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":4709559,"end":4742043,"strand":-1,"description":"adenylate kinase 3 [Source:HGNC Symbol;Acc:HGNC:17376]"}, {"versioned_ensembl_gene_id":"ENSG00000258986.6","gene_symbol":"TMEM179","gene_name":"transmembrane protein 179 [Source:HGNC Symbol;Acc:HGNC:20137]","synonyms":"C14orf90,TMEM179A,FLJ42486","biotype":"protein_coding","ncbi_id":"388021","summary":null,"start":104474678,"end":104605647,"strand":-1,"description":"transmembrane protein 179 [Source:HGNC Symbol;Acc:HGNC:20137]"}, {"versioned_ensembl_gene_id":"ENSG00000108010.11","gene_symbol":"GLRX3","gene_name":"glutaredoxin 3 [Source:HGNC Symbol;Acc:HGNC:15987]","synonyms":"TXNL2,PICOT,GRX4,GRX3,GLRX4,bA500G10.4","biotype":"protein_coding","ncbi_id":"10539","summary":"This gene encodes a member of the glutaredoxin family. Glutaredoxins are oxidoreductase enzymes that reduce a variety of substrates using glutathione as a cofactor. The encoded protein binds to and modulates the function of protein kinase C theta. The encoded protein may also inhibit apoptosis and play a role in cellular growth, and the expression of this gene may be a marker for cancer. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 9. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]","start":130136399,"end":130184521,"strand":1,"description":"glutaredoxin 3 [Source:HGNC Symbol;Acc:HGNC:15987]"}, {"versioned_ensembl_gene_id":"ENSG00000230950.1","gene_symbol":"MTND2P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42122]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873227","summary":null,"start":117025077,"end":117026118,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42122]"}, {"versioned_ensembl_gene_id":"ENSG00000235871.1","gene_symbol":"AC062016.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116818086,"end":116818761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226341.1","gene_symbol":"MTCYBP39","gene_name":"mitochondrially encoded cytochrome b pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52307]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729152","summary":null,"start":116751158,"end":116751648,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52307]"}, {"versioned_ensembl_gene_id":"ENSG00000163071.10","gene_symbol":"SPATA18","gene_name":"spermatogenesis associated 18 [Source:HGNC Symbol;Acc:HGNC:29579]","synonyms":"FLJ32906","biotype":"protein_coding","ncbi_id":"132671","summary":"This gene encodes a p53-inducible protein that is able to induce lysosome-like organelles within mitochondria that eliminate oxidized mitochondrial proteins, thereby contributing to mitochondrial quality control. Dysregulation of mitochondrial quality control is associated with cancer and degenerative diseases. The encoded protein mediates accumulation of the lysosome-like mitochondrial organelles through interaction with B cell lymphoma 2 interacting protein 3 and B cell lymphoma 2 interacting protein 3 like at the outer mitochondrial membrane, which allows translocation of lysosomal proteins to the mitochondrial matrix from the cytosol. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":52051331,"end":52097292,"strand":1,"description":"spermatogenesis associated 18 [Source:HGNC Symbol;Acc:HGNC:29579]"}, {"versioned_ensembl_gene_id":"ENSG00000239704.10","gene_symbol":"CDRT4","gene_name":"CMT1A duplicated region transcript 4 [Source:HGNC Symbol;Acc:HGNC:14383]","synonyms":"FLJ36674","biotype":"protein_coding","ncbi_id":"284040","summary":null,"start":15436015,"end":15503608,"strand":-1,"description":"CMT1A duplicated region transcript 4 [Source:HGNC Symbol;Acc:HGNC:14383]"}, {"versioned_ensembl_gene_id":"ENSG00000203734.11","gene_symbol":"ECT2L","gene_name":"epithelial cell transforming 2 like [Source:HGNC Symbol;Acc:HGNC:21118]","synonyms":"LFDH,FBXO49,C6orf91,ARHGEF32","biotype":"protein_coding","ncbi_id":"345930","summary":null,"start":138795926,"end":138904070,"strand":1,"description":"epithelial cell transforming 2 like [Source:HGNC Symbol;Acc:HGNC:21118]"}, {"versioned_ensembl_gene_id":"ENSG00000228106.5","gene_symbol":"AL392172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222815022,"end":222837384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259024.6","gene_symbol":"TVP23C-CDRT4","gene_name":"TVP23C-CDRT4 readthrough [Source:HGNC Symbol;Acc:HGNC:42961]","synonyms":"FAM18B2-CDRT4","biotype":"protein_coding","ncbi_id":"100533496","summary":"This locus represents naturally occurring readthrough transcription between the neighboring TVP23C (trans-golgi network vesicle protein 23 homolog) and CDRT4 (CMT1A duplicated region transcript 4) genes on chromosome 17. Alternative splicing results in multiple transcript variants, one of which encodes a protein that shares sequence identity with the upstream gene product, but its C-terminus is distinct due to frameshifts relative to the downstream gene. [provided by RefSeq, Apr 2014]","start":15436021,"end":15563561,"strand":-1,"description":"TVP23C-CDRT4 readthrough [Source:HGNC Symbol;Acc:HGNC:42961]"}, {"versioned_ensembl_gene_id":"ENSG00000179603.17","gene_symbol":"GRM8","gene_name":"glutamate metabotropic receptor 8 [Source:HGNC Symbol;Acc:HGNC:4600]","synonyms":"MGLUR8,mGlu8,GPRC1H,GLUR8","biotype":"protein_coding","ncbi_id":"2918","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":126438598,"end":127253294,"strand":-1,"description":"glutamate metabotropic receptor 8 [Source:HGNC Symbol;Acc:HGNC:4600]"}, {"versioned_ensembl_gene_id":"ENSG00000257803.2","gene_symbol":"AC010200.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100578744,"end":100580197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172236.16","gene_symbol":"TPSAB1","gene_name":"tryptase alpha/beta 1 [Source:HGNC Symbol;Acc:HGNC:12019]","synonyms":"TPSB1,TPS2,TPS1","biotype":"protein_coding","ncbi_id":"7177","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. These genes are characterized by several distinct features. They have a highly conserved 3' UTR and contain tandem repeat sequences at the 5' flank and 3' UTR which are thought to play a role in regulation of the mRNA stability. These genes have an intron immediately upstream of the initiator Met codon, which separates the site of transcription initiation from protein coding sequence. This feature is characteristic of tryptases but is unusual in other genes. The alleles of this gene exhibit an unusual amount of sequence variation, such that the alleles were once thought to represent two separate genes, alpha and beta 1. Beta tryptases appear to be the main isoenzymes expressed in mast cells; whereas in basophils, alpha tryptases predominate. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq, Jul 2008]","start":1240696,"end":1242554,"strand":1,"description":"tryptase alpha/beta 1 [Source:HGNC Symbol;Acc:HGNC:12019]"}, {"versioned_ensembl_gene_id":"ENSG00000114853.13","gene_symbol":"ZBTB47","gene_name":"zinc finger and BTB domain containing 47 [Source:HGNC Symbol;Acc:HGNC:26955]","synonyms":"KIAA1190,DKFZp434N0615,ZNF651","biotype":"protein_coding","ncbi_id":"92999","summary":null,"start":42653684,"end":42665854,"strand":1,"description":"zinc finger and BTB domain containing 47 [Source:HGNC Symbol;Acc:HGNC:26955]"}, {"versioned_ensembl_gene_id":"ENSG00000064726.9","gene_symbol":"BTBD1","gene_name":"BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1120]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53339","summary":"The C-terminus of the protein encoded by this gene binds topoisomerase I. The N-terminus contains a proline-rich region and a BTB/POZ domain (broad-complex, Tramtrack and bric a brac/Pox virus and Zinc finger), both of which are typically involved in protein-protein interactions. Subcellularly, the protein localizes to cytoplasmic bodies. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":83016422,"end":83067354,"strand":-1,"description":"BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1120]"}, {"versioned_ensembl_gene_id":"ENSG00000272913.1","gene_symbol":"AC009237.14","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95525109,"end":95526702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226976.3","gene_symbol":"COX6A1P2","gene_name":"cytochrome c oxidase subunit 6A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285849","summary":null,"start":37044860,"end":37045189,"strand":1,"description":"cytochrome c oxidase subunit 6A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35239]"}, {"versioned_ensembl_gene_id":"ENSG00000279749.1","gene_symbol":"AC093875.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":136553236,"end":136553739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224935.1","gene_symbol":"AL589678.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12098660,"end":12159147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117155.16","gene_symbol":"SSX2IP","gene_name":"SSX family member 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:16509]","synonyms":"hMsd1","biotype":"protein_coding","ncbi_id":"117178","summary":"This gene encodes a protein that binds the cancer-testis antigen Synovial Sarcoma X breakpoint 2 protein. The encoded protein may regulate the activity of Synovial Sarcoma X breakpoint 2 protein in malignant cells. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Oct 2009]","start":84643707,"end":84690803,"strand":-1,"description":"SSX family member 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:16509]"}, {"versioned_ensembl_gene_id":"ENSG00000236490.9","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33277619,"end":33292309,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000169894.17","gene_symbol":"MUC3A","gene_name":"mucin 3A, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7513]","synonyms":"MUC3","biotype":"protein_coding","ncbi_id":"4584","summary":"The mucin genes encode epithelial glycoproteins, some of which are secreted and some membrane bound. Each of the genes contains at least one large domain of tandemly repeated sequence that encodes the peptide sequence rich in serine and/or threonine residues, which carries most of the O-linked glycosylation (Gendler and Spicer, 1995 [PubMed 7778880]).[supplied by OMIM, Aug 2008]","start":100949555,"end":100968346,"strand":1,"description":"mucin 3A, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7513]"}, {"versioned_ensembl_gene_id":"ENSG00000184601.10","gene_symbol":"C14orf180","gene_name":"chromosome 14 open reading frame 180 [Source:HGNC Symbol;Acc:HGNC:33795]","synonyms":"NRAC,C14orf77","biotype":"protein_coding","ncbi_id":"400258","summary":null,"start":104579684,"end":104590515,"strand":1,"description":"chromosome 14 open reading frame 180 [Source:HGNC Symbol;Acc:HGNC:33795]"}, {"versioned_ensembl_gene_id":"ENSG00000228013.1","gene_symbol":"AL162591.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154402328,"end":154406564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235254.3","gene_symbol":"TMEM185AP1","gene_name":"transmembrane protein 185A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31717]","synonyms":"TMEM185AL","biotype":"unprocessed_pseudogene","ncbi_id":"100506205","summary":null,"start":149768897,"end":149771368,"strand":1,"description":"transmembrane protein 185A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31717]"}, {"versioned_ensembl_gene_id":"ENSG00000166007.11","gene_symbol":"TRIM51HP","gene_name":"tripartite motif-containing 51H, pseudogene [Source:HGNC Symbol;Acc:HGNC:43977]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440041","summary":null,"start":55291883,"end":55298270,"strand":-1,"description":"tripartite motif-containing 51H, pseudogene [Source:HGNC Symbol;Acc:HGNC:43977]"}, {"versioned_ensembl_gene_id":"ENSG00000273797.1","gene_symbol":"AL133445.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":69617122,"end":69617648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146247.13","gene_symbol":"PHIP","gene_name":"pleckstrin homology domain interacting protein [Source:HGNC Symbol;Acc:HGNC:15673]","synonyms":"WDR11,ndrp,FLJ20705,DCAF14,BRWD2","biotype":"protein_coding","ncbi_id":"55023","summary":"This gene encodes a protein that binds to the insulin receptor substrate 1 protein and regulates glucose transporter translocation in skeletal muscle cells. The encoded protein may also regulate growth and survival of pancreatic beta cells. Elevated copy number of this gene may be associated with melanoma severity and the encoded protein may promote melanoma metastasis in human patients. [provided by RefSeq, Oct 2016]","start":78935867,"end":79078236,"strand":-1,"description":"pleckstrin homology domain interacting protein [Source:HGNC Symbol;Acc:HGNC:15673]"}, {"versioned_ensembl_gene_id":"ENSG00000237377.2","gene_symbol":"AC005703.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15276562,"end":15279477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085063.14","gene_symbol":"CD59","gene_name":"CD59 molecule (CD59 blood group) [Source:HGNC Symbol;Acc:HGNC:1689]","synonyms":"MIC11,G344,EL32,EJ30,p18-20,EJ16,MSK21,16.3A5,MIN3,MIN2,MIN1","biotype":"protein_coding","ncbi_id":"966","summary":"This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":33698261,"end":33736445,"strand":-1,"description":"CD59 molecule (CD59 blood group) [Source:HGNC Symbol;Acc:HGNC:1689]"}, {"versioned_ensembl_gene_id":"ENSG00000258071.1","gene_symbol":"ARL2BPP2","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31036]","synonyms":"bcm1040,ARL2BPL","biotype":"processed_pseudogene","ncbi_id":"643898","summary":null,"start":52763405,"end":52763893,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31036]"}, {"versioned_ensembl_gene_id":"ENSG00000132744.7","gene_symbol":"ACY3","gene_name":"aminoacylase 3 [Source:HGNC Symbol;Acc:HGNC:24104]","synonyms":"MGC9740,HCBP1,ACY-3","biotype":"protein_coding","ncbi_id":"91703","summary":null,"start":67642555,"end":67650659,"strand":-1,"description":"aminoacylase 3 [Source:HGNC Symbol;Acc:HGNC:24104]"}, {"versioned_ensembl_gene_id":"ENSG00000250391.1","gene_symbol":"AC092284.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99948295,"end":99949583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255145.2","gene_symbol":"STX17-AS1","gene_name":"STX17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51174]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"441461","summary":null,"start":99886322,"end":99906601,"strand":-1,"description":"STX17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51174]"}, {"versioned_ensembl_gene_id":"ENSG00000229533.1","gene_symbol":"AC003986.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19144293,"end":19146253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225723.1","gene_symbol":"MTND6P15","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39478]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478949","summary":null,"start":237949214,"end":237949734,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39478]"}, {"versioned_ensembl_gene_id":"ENSG00000235060.1","gene_symbol":"VDAC1P4","gene_name":"voltage dependent anion channel 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:12675]","synonyms":"VDAC4P,VDAC4","biotype":"processed_pseudogene","ncbi_id":"7418","summary":"VDAC4 belongs to a family of small, abundant pore-forming proteins found in the outer mitochondrial membrane. These channels are thought to form the major pathway for movement of adenine nucleotides through the outer membrane and may also function as the mitochondrial binding site for hexokinase (see HK1; MIM 142600) and glycerol kinase (GK; MIM 300474) (Blachly-Dyson et al., 1994 [PubMed 7517385]).[supplied by OMIM, Mar 2008]","start":180434800,"end":180435936,"strand":1,"description":"voltage dependent anion channel 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:12675]"}, {"versioned_ensembl_gene_id":"ENSG00000244237.1","gene_symbol":"AL133445.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69561019,"end":69561470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219061.4","gene_symbol":"TRIM51FP","gene_name":"tripartite motif-containing 51F, pseudogene [Source:HGNC Symbol;Acc:HGNC:43966]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"283257","summary":null,"start":49833140,"end":49839320,"strand":-1,"description":"tripartite motif-containing 51F, pseudogene [Source:HGNC Symbol;Acc:HGNC:43966]"}, {"versioned_ensembl_gene_id":"ENSG00000246465.1","gene_symbol":"AC138904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28284885,"end":28292064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223539.4","gene_symbol":"AC011431.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135742462,"end":135746356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174928.15","gene_symbol":"C3orf33","gene_name":"chromosome 3 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:26434]","synonyms":"AC3-33,FLJ31139","biotype":"protein_coding","ncbi_id":"285315","summary":null,"start":155762617,"end":155806351,"strand":-1,"description":"chromosome 3 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:26434]"}, {"versioned_ensembl_gene_id":"ENSG00000281180.1","gene_symbol":"AP000350.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23865248,"end":23873277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196531.10","gene_symbol":"NACA","gene_name":"nascent polypeptide-associated complex alpha subunit [Source:HGNC Symbol;Acc:HGNC:7629]","synonyms":"NACA1","biotype":"protein_coding","ncbi_id":"4666","summary":"This gene encodes a protein that associates with basic transcription factor 3 (BTF3) to form the nascent polypeptide-associated complex (NAC). This complex binds to nascent proteins that lack a signal peptide motif as they emerge from the ribosome, blocking interaction with the signal recognition particle (SRP) and preventing mistranslocation to the endoplasmic reticulum. This protein is an IgE autoantigen in atopic dermatitis patients. Alternative splicing results in multiple transcript variants, but the full length nature of some of these variants, including those encoding very large proteins, has not been determined. There are multiple pseudogenes of this gene on different chromosomes. [provided by RefSeq, Feb 2016]","start":56712428,"end":56731628,"strand":-1,"description":"nascent polypeptide-associated complex alpha subunit [Source:HGNC Symbol;Acc:HGNC:7629]"}, {"versioned_ensembl_gene_id":"ENSG00000124467.18","gene_symbol":"PSG8","gene_name":"pregnancy specific beta-1-glycoprotein 8 [Source:HGNC Symbol;Acc:HGNC:9525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440533","summary":"The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":42752686,"end":42855691,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 8 [Source:HGNC Symbol;Acc:HGNC:9525]"}, {"versioned_ensembl_gene_id":"ENSG00000230084.5","gene_symbol":"AC006059.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42601963,"end":42654388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000051620.10","gene_symbol":"HEBP2","gene_name":"heme binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15716]","synonyms":"SOUL,C6orf34","biotype":"protein_coding","ncbi_id":"23593","summary":"The protein encoded by this gene is found predominately in the cytoplasm, where it plays a role in the collapse of mitochondrial membrane potential (MMP) prior to necrotic cell death. The encoded protein enhances outer and inner mitochondrial membrane permeabilization, especially under conditions of oxidative stress. [provided by RefSeq, May 2016]","start":138403531,"end":138422197,"strand":1,"description":"heme binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15716]"}, {"versioned_ensembl_gene_id":"ENSG00000107957.16","gene_symbol":"SH3PXD2A","gene_name":"SH3 and PX domains 2A [Source:HGNC Symbol;Acc:HGNC:23664]","synonyms":"SH3MD1,KIAA0418,FISH","biotype":"protein_coding","ncbi_id":"9644","summary":null,"start":103594027,"end":103855543,"strand":-1,"description":"SH3 and PX domains 2A [Source:HGNC Symbol;Acc:HGNC:23664]"}, {"versioned_ensembl_gene_id":"ENSG00000238092.1","gene_symbol":"CEACAMP6","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:1828]","synonyms":"CGM13","biotype":"unprocessed_pseudogene","ncbi_id":"1094","summary":null,"start":42781206,"end":42786595,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:1828]"}, {"versioned_ensembl_gene_id":"ENSG00000186340.14","gene_symbol":"THBS2","gene_name":"thrombospondin 2 [Source:HGNC Symbol;Acc:HGNC:11786]","synonyms":"TSP2","biotype":"protein_coding","ncbi_id":"7058","summary":"The protein encoded by this gene belongs to the thrombospondin family. It is a disulfide-linked homotrimeric glycoprotein that mediates cell-to-cell and cell-to-matrix interactions. This protein has been shown to function as a potent inhibitor of tumor growth and angiogenesis. Studies of the mouse counterpart suggest that this protein may modulate the cell surface properties of mesenchymal cells and be involved in cell adhesion and migration. [provided by RefSeq, Jul 2008]","start":169215780,"end":169254044,"strand":-1,"description":"thrombospondin 2 [Source:HGNC Symbol;Acc:HGNC:11786]"}, {"versioned_ensembl_gene_id":"ENSG00000188620.9","gene_symbol":"HMX3","gene_name":"H6 family homeobox 3 [Source:HGNC Symbol;Acc:HGNC:5019]","synonyms":"NKX5-1","biotype":"protein_coding","ncbi_id":"340784","summary":null,"start":123135962,"end":123137741,"strand":1,"description":"H6 family homeobox 3 [Source:HGNC Symbol;Acc:HGNC:5019]"}, {"versioned_ensembl_gene_id":"ENSG00000143515.16","gene_symbol":"ATP8B2","gene_name":"ATPase phospholipid transporting 8B2 [Source:HGNC Symbol;Acc:HGNC:13534]","synonyms":"KIAA1137,ATPID","biotype":"protein_coding","ncbi_id":"57198","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":154325553,"end":154351307,"strand":1,"description":"ATPase phospholipid transporting 8B2 [Source:HGNC Symbol;Acc:HGNC:13534]"}, {"versioned_ensembl_gene_id":"ENSG00000254769.3","gene_symbol":"OR4A4P","gene_name":"olfactory receptor family 4 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15161]","synonyms":"OR4A4","biotype":"unprocessed_pseudogene","ncbi_id":"390134","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54659666,"end":54660595,"strand":1,"description":"olfactory receptor family 4 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15161]"}, {"versioned_ensembl_gene_id":"ENSG00000276898.1","gene_symbol":"BX664730.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67512034,"end":67515393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105499.13","gene_symbol":"PLA2G4C","gene_name":"phospholipase A2 group IVC [Source:HGNC Symbol;Acc:HGNC:9037]","synonyms":"cPLA2-gamma","biotype":"protein_coding","ncbi_id":"8605","summary":"This gene encodes a protein which is a member of the phospholipase A2 enzyme family which hydrolyzes glycerophospholipids to produce free fatty acids and lysophospholipids, both of which serve as precursors in the production of signaling molecules. The encoded protein has been shown to be a calcium-independent and membrane bound enzyme. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]","start":48047843,"end":48110817,"strand":-1,"description":"phospholipase A2 group IVC [Source:HGNC Symbol;Acc:HGNC:9037]"}, {"versioned_ensembl_gene_id":"ENSG00000271945.1","gene_symbol":"AL590426.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76774983,"end":76775860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255312.1","gene_symbol":"OR4C7P","gene_name":"olfactory receptor family 4 subfamily C member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14768]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79294","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54635037,"end":54635955,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14768]"}, {"versioned_ensembl_gene_id":"ENSG00000178934.4","gene_symbol":"LGALS7B","gene_name":"galectin 7B [Source:HGNC Symbol;Acc:HGNC:34447]","synonyms":"GAL7","biotype":"protein_coding","ncbi_id":"653499","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:3963) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008]","start":38789211,"end":38791749,"strand":1,"description":"galectin 7B [Source:HGNC Symbol;Acc:HGNC:34447]"}, {"versioned_ensembl_gene_id":"ENSG00000080573.6","gene_symbol":"COL5A3","gene_name":"collagen type V alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:14864]","synonyms":null,"biotype":"protein_coding","ncbi_id":"50509","summary":"This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. Mutations in this gene are thought to be responsible for the symptoms of a subset of patients with Ehlers-Danlos syndrome type III. Messages of several sizes can be detected in northern blots but sequence information cannot confirm the identity of the shorter messages. [provided by RefSeq, Jul 2008]","start":9959561,"end":10010471,"strand":-1,"description":"collagen type V alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:14864]"}, {"versioned_ensembl_gene_id":"ENSG00000172421.8","gene_symbol":"EFCAB3","gene_name":"EF-hand calcium binding domain 3 [Source:HGNC Symbol;Acc:HGNC:26379]","synonyms":"FLJ25818","biotype":"protein_coding","ncbi_id":"146779","summary":null,"start":62343941,"end":62416479,"strand":1,"description":"EF-hand calcium binding domain 3 [Source:HGNC Symbol;Acc:HGNC:26379]"}, {"versioned_ensembl_gene_id":"ENSG00000259649.4","gene_symbol":"AC027808.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80896191,"end":80909777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282535.1","gene_symbol":"AC092192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176896,"end":177913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134748.12","gene_symbol":"PRPF38A","gene_name":"pre-mRNA processing factor 38A [Source:HGNC Symbol;Acc:HGNC:25930]","synonyms":"Prp38,FLJ14936","biotype":"protein_coding","ncbi_id":"84950","summary":null,"start":52404564,"end":52420839,"strand":1,"description":"pre-mRNA processing factor 38A [Source:HGNC Symbol;Acc:HGNC:25930]"}, {"versioned_ensembl_gene_id":"ENSG00000254931.2","gene_symbol":"MTATP6P15","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52060]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075273","summary":null,"start":103402588,"end":103403422,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52060]"}, {"versioned_ensembl_gene_id":"ENSG00000254518.1","gene_symbol":"AC109635.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50298579,"end":50304656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248846.2","gene_symbol":"LINC02065","gene_name":"long intergenic non-protein coding RNA 2065 [Source:HGNC Symbol;Acc:HGNC:52910]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928741","summary":null,"start":66206212,"end":66209447,"strand":-1,"description":"long intergenic non-protein coding RNA 2065 [Source:HGNC Symbol;Acc:HGNC:52910]"}, {"versioned_ensembl_gene_id":"ENSG00000065526.10","gene_symbol":"SPEN","gene_name":"spen family transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:17575]","synonyms":"SHARP,RBM15C,MINT,KIAA0929","biotype":"protein_coding","ncbi_id":"23013","summary":"This gene encodes a hormone inducible transcriptional repressor. Repression of transcription by this gene product can occur through interactions with other repressors, by the recruitment of proteins involved in histone deacetylation, or through sequestration of transcriptional activators. The product of this gene contains a carboxy-terminal domain that permits binding to other corepressor proteins. This domain also permits interaction with members of the NuRD complex, a nucleosome remodeling protein complex that contains deacetylase activity. In addition, this repressor contains several RNA recognition motifs that confer binding to a steroid receptor RNA coactivator; this binding can modulate the activity of both liganded and nonliganded steroid receptors. [provided by RefSeq, Jul 2008]","start":15847864,"end":15940460,"strand":1,"description":"spen family transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:17575]"}, {"versioned_ensembl_gene_id":"ENSG00000269188.1","gene_symbol":"AC011500.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39584042,"end":39586489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179921.14","gene_symbol":"GPBAR1","gene_name":"G protein-coupled bile acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:19680]","synonyms":"TGR5,MGC40597,M-BAR,GPR131,GPCR19,GPCR,BG37","biotype":"protein_coding","ncbi_id":"151306","summary":"This gene encodes a member of the G protein-coupled receptor (GPCR) superfamily. This enzyme functions as a cell surface receptor for bile acids. Treatment of cells expressing this GPCR with bile acids induces the production of intracellular cAMP, activation of a MAP kinase signaling pathway, and internalization of the receptor. The receptor is implicated in the suppression of macrophage functions and regulation of energy homeostasis by bile acids. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":218259496,"end":218263859,"strand":1,"description":"G protein-coupled bile acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:19680]"}, {"versioned_ensembl_gene_id":"ENSG00000255313.1","gene_symbol":"AC100858.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124936524,"end":124943765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278641.1","gene_symbol":"DUX4L15","gene_name":"double homeobox 4 like 15 [Source:HGNC Symbol;Acc:HGNC:38674]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440017","summary":null,"start":133759859,"end":133761125,"strand":1,"description":"double homeobox 4 like 15 [Source:HGNC Symbol;Acc:HGNC:38674]"}, {"versioned_ensembl_gene_id":"ENSG00000242711.8","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32883408,"end":32918836,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000276904.1","gene_symbol":"DUX4L14","gene_name":"double homeobox 4 like 14 [Source:HGNC Symbol;Acc:HGNC:38673]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728022","summary":null,"start":133756559,"end":133757825,"strand":1,"description":"double homeobox 4 like 14 [Source:HGNC Symbol;Acc:HGNC:38673]"}, {"versioned_ensembl_gene_id":"ENSG00000237790.1","gene_symbol":"LINC01318","gene_name":"long intergenic non-protein coding RNA 1318 [Source:HGNC Symbol;Acc:HGNC:50524]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144585","summary":null,"start":34067226,"end":34069550,"strand":1,"description":"long intergenic non-protein coding RNA 1318 [Source:HGNC Symbol;Acc:HGNC:50524]"}, {"versioned_ensembl_gene_id":"ENSG00000253206.1","gene_symbol":"AC090155.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49536386,"end":49554414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151474.21","gene_symbol":"FRMD4A","gene_name":"FERM domain containing 4A [Source:HGNC Symbol;Acc:HGNC:25491]","synonyms":"KIAA1294,FRMD4,FLJ10210,bA295P9.4","biotype":"protein_coding","ncbi_id":"55691","summary":"This gene encodes a FERM domain-containing protein that regulates epithelial cell polarity. It connects ADP ribosylation factor 6 (ARF6) with the Par protein complex, which regulates the remodeling of adherens junctions and linear actin cable formation during epithelial cell polarization. Polymorphisms in this gene are associated with Alzheimer's disease, and also with nicotine dependence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":13643706,"end":14462142,"strand":-1,"description":"FERM domain containing 4A [Source:HGNC Symbol;Acc:HGNC:25491]"}, {"versioned_ensembl_gene_id":"ENSG00000244432.2","gene_symbol":"RPL39P28","gene_name":"ribosomal protein L39 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35619]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271520","summary":null,"start":68001394,"end":68001548,"strand":-1,"description":"ribosomal protein L39 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35619]"}, {"versioned_ensembl_gene_id":"ENSG00000226617.1","gene_symbol":"RPL21P110","gene_name":"ribosomal protein L21 pseudogene 110 [Source:HGNC Symbol;Acc:HGNC:35627]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271438","summary":null,"start":72703693,"end":72704138,"strand":1,"description":"ribosomal protein L21 pseudogene 110 [Source:HGNC Symbol;Acc:HGNC:35627]"}, {"versioned_ensembl_gene_id":"ENSG00000249722.1","gene_symbol":"AC025752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174329612,"end":174330503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167972.13","gene_symbol":"ABCA3","gene_name":"ATP binding cassette subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:33]","synonyms":"LBM180,EST111653,ABC3,ABC-C","biotype":"protein_coding","ncbi_id":"21","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The full transporter encoded by this gene may be involved in development of resistance to xenobiotics and engulfment during programmed cell death. [provided by RefSeq, Jul 2008]","start":2275881,"end":2340746,"strand":-1,"description":"ATP binding cassette subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:33]"}, {"versioned_ensembl_gene_id":"ENSG00000271900.1","gene_symbol":"AC025627.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19601840,"end":19602256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183655.12","gene_symbol":"KLHL25","gene_name":"kelch like family member 25 [Source:HGNC Symbol;Acc:HGNC:25732]","synonyms":"FLJ12587,ENC2,ENC-2","biotype":"protein_coding","ncbi_id":"64410","summary":null,"start":85759323,"end":85795030,"strand":-1,"description":"kelch like family member 25 [Source:HGNC Symbol;Acc:HGNC:25732]"}, {"versioned_ensembl_gene_id":"ENSG00000230623.4","gene_symbol":"AC104461.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":200333193,"end":200478293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263199.1","gene_symbol":"AC005951.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54702936,"end":54703430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150967.17","gene_symbol":"ABCB9","gene_name":"ATP binding cassette subfamily B member 9 [Source:HGNC Symbol;Acc:HGNC:50]","synonyms":"EST122234","biotype":"protein_coding","ncbi_id":"23457","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This family member functions in the translocation of peptides from the cytosol into the lysosomal lumen. Alternative splicing of this gene results in distinct isoforms which are likely to have different substrate specificities. [provided by RefSeq, Jul 2011]","start":122920951,"end":122981649,"strand":-1,"description":"ATP binding cassette subfamily B member 9 [Source:HGNC Symbol;Acc:HGNC:50]"}, {"versioned_ensembl_gene_id":"ENSG00000261965.1","gene_symbol":"ISCA1P3","gene_name":"iron-sulfur cluster assembly 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38024]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131092","summary":null,"start":54477796,"end":54478168,"strand":1,"description":"iron-sulfur cluster assembly 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38024]"}, {"versioned_ensembl_gene_id":"ENSG00000276521.1","gene_symbol":"AP001486.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102963460,"end":102966628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179142.2","gene_symbol":"CYP11B2","gene_name":"cytochrome P450 family 11 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:2592]","synonyms":"P450aldo,P-450C18,CYP11BL,CYP11B,CPN2,ALDOS","biotype":"protein_coding","ncbi_id":"1585","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008]","start":142910559,"end":142917843,"strand":-1,"description":"cytochrome P450 family 11 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:2592]"}, {"versioned_ensembl_gene_id":"ENSG00000262384.1","gene_symbol":"AC034268.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53681630,"end":53682111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226407.1","gene_symbol":"RPL23P11","gene_name":"ribosomal protein L23 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271297","summary":null,"start":33864313,"end":33864723,"strand":1,"description":"ribosomal protein L23 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36457]"}, {"versioned_ensembl_gene_id":"ENSG00000185022.11","gene_symbol":"MAFF","gene_name":"MAF bZIP transcription factor F [Source:HGNC Symbol;Acc:HGNC:6780]","synonyms":"hMafF","biotype":"protein_coding","ncbi_id":"23764","summary":"The protein encoded by this gene is a basic leucine zipper (bZIP) transcription factor that lacks a transactivation domain. It is known to bind the US-2 DNA element in the promoter of the oxytocin receptor (OTR) gene and most likely heterodimerizes with other leucine zipper-containing proteins to enhance expression of the OTR gene during term pregnancy. The encoded protein can also form homodimers, and since it lacks a transactivation domain, the homodimer may act as a repressor of transcription. This gene may also be involved in the cellular stress response. Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":38200767,"end":38216511,"strand":1,"description":"MAF bZIP transcription factor F [Source:HGNC Symbol;Acc:HGNC:6780]"}, {"versioned_ensembl_gene_id":"ENSG00000268543.1","gene_symbol":"AC012313.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58418560,"end":58419310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119411.10","gene_symbol":"BSPRY","gene_name":"B-box and SPRY domain containing [Source:HGNC Symbol;Acc:HGNC:18232]","synonyms":"FLJ20150","biotype":"protein_coding","ncbi_id":"54836","summary":null,"start":113349541,"end":113371233,"strand":1,"description":"B-box and SPRY domain containing [Source:HGNC Symbol;Acc:HGNC:18232]"}, {"versioned_ensembl_gene_id":"ENSG00000116824.4","gene_symbol":"CD2","gene_name":"CD2 molecule [Source:HGNC Symbol;Acc:HGNC:1639]","synonyms":"SRBC","biotype":"protein_coding","ncbi_id":"914","summary":"The protein encoded by this gene is a surface antigen found on all peripheral blood T-cells. The encoded protein interacts with LFA3 (CD58) on antigen presenting cells to optimize immune recognition. A locus control region (LCR) has been found in the 3' flanking sequence of this gene. [provided by RefSeq, Jun 2016]","start":116754385,"end":116769228,"strand":1,"description":"CD2 molecule [Source:HGNC Symbol;Acc:HGNC:1639]"}, {"versioned_ensembl_gene_id":"ENSG00000160097.16","gene_symbol":"FNDC5","gene_name":"fibronectin type III domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20240]","synonyms":"FRCP2","biotype":"protein_coding","ncbi_id":"252995","summary":"This gene encodes a secreted protein that is released from muscle cells during exercise. The encoded protein may participate in the development of brown fat. Translation of the precursor protein initiates at a non-AUG start codon at a position that is conserved as an AUG start codon in other organisms. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":32862268,"end":32872482,"strand":-1,"description":"fibronectin type III domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20240]"}, {"versioned_ensembl_gene_id":"ENSG00000170484.9","gene_symbol":"KRT74","gene_name":"keratin 74 [Source:HGNC Symbol;Acc:HGNC:28929]","synonyms":"KRT6IRS4,KRT5C,K6IRS4","biotype":"protein_coding","ncbi_id":"121391","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This protein belongs to a family of keratins that are specifically expressed in the inner root sheath of hair follicles.[provided by RefSeq, Jun 2009]","start":52565782,"end":52573825,"strand":-1,"description":"keratin 74 [Source:HGNC Symbol;Acc:HGNC:28929]"}, {"versioned_ensembl_gene_id":"ENSG00000265552.1","gene_symbol":"AC104961.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25055600,"end":25056760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049239.12","gene_symbol":"H6PD","gene_name":"hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4795]","synonyms":"GDH","biotype":"protein_coding","ncbi_id":"9563","summary":"There are 2 forms of glucose-6-phosphate dehydrogenase. G form is X-linked and H form, encoded by this gene, is autosomally linked. This H form shows activity with other hexose-6-phosphates, especially galactose-6-phosphate, whereas the G form is specific for glucose-6-phosphate. Both forms are present in most tissues, but H form is not found in red cells. [provided by RefSeq, Jul 2008]","start":9234775,"end":9271337,"strand":1,"description":"hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4795]"}, {"versioned_ensembl_gene_id":"ENSG00000275356.3","gene_symbol":"C7orf77","gene_name":"chromosome 7 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:51256]","synonyms":null,"biotype":"protein_coding","ncbi_id":"154872","summary":null,"start":124777292,"end":124790689,"strand":-1,"description":"chromosome 7 open reading frame 77 [Source:HGNC Symbol;Acc:HGNC:51256]"}, {"versioned_ensembl_gene_id":"ENSG00000164825.3","gene_symbol":"DEFB1","gene_name":"defensin beta 1 [Source:HGNC Symbol;Acc:HGNC:2766]","synonyms":"MGC51822,HBD1,HBD-1,DEFB101,DEFB-1,BD1","biotype":"protein_coding","ncbi_id":"1672","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 1, an antimicrobial peptide implicated in the resistance of epithelial surfaces to microbial colonization. This gene maps in close proximity to defensin family member, defensin, alpha 1 and has been implicated in the pathogenesis of cystic fibrosis. [provided by RefSeq, Jul 2008]","start":6870575,"end":6878022,"strand":-1,"description":"defensin beta 1 [Source:HGNC Symbol;Acc:HGNC:2766]"}, {"versioned_ensembl_gene_id":"ENSG00000237663.2","gene_symbol":"DNAJC19P7","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861458","summary":null,"start":52252062,"end":52252773,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45070]"}, {"versioned_ensembl_gene_id":"ENSG00000228407.2","gene_symbol":"AL139156.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52160261,"end":52160600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231072.1","gene_symbol":"GAPDHP64","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:4158]","synonyms":"GAPDL9,GAPDHL9","biotype":"processed_pseudogene","ncbi_id":"391069","summary":null,"start":116713833,"end":116714835,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:4158]"}, {"versioned_ensembl_gene_id":"ENSG00000259495.2","gene_symbol":"AC016705.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80344853,"end":80403575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283686.2","gene_symbol":"AC083841.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":142797624,"end":142806142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253715.1","gene_symbol":"AC083841.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142785374,"end":142812120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175166.16","gene_symbol":"PSMD2","gene_name":"proteasome 26S subunit, non-ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9559]","synonyms":"TRAP2,S2,Rpn1,P97,MGC14274","biotype":"protein_coding","ncbi_id":"5708","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the non-ATPase subunits of the 19S regulator lid. In addition to participation in proteasome function, this subunit may also participate in the TNF signalling pathway since it interacts with the tumor necrosis factor type 1 receptor. A pseudogene has been identified on chromosome 1. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":184298709,"end":184309054,"strand":1,"description":"proteasome 26S subunit, non-ATPase 2 [Source:HGNC Symbol;Acc:HGNC:9559]"}, {"versioned_ensembl_gene_id":"ENSG00000232995.7","gene_symbol":"RGS5","gene_name":"regulator of G protein signaling 5 [Source:NCBI gene;Acc:8490]","synonyms":"MSTP106,MSTP092,MSTP032,MST129,MST106,MST092,MSTP129","biotype":"antisense_RNA","ncbi_id":"8490","summary":"This gene encodes a member of the regulators of G protein signaling (RGS) family. The RGS proteins are signal transduction molecules which are involved in the regulation of heterotrimeric G proteins by acting as GTPase activators. This gene is a hypoxia-inducible factor-1 dependent, hypoxia-induced gene which is involved in the induction of endothelial apoptosis. This gene is also one of three genes on chromosome 1q contributing to elevated blood pressure. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Dec 2011]","start":163244505,"end":163321894,"strand":-1,"description":"regulator of G protein signaling 5 [Source:NCBI gene;Acc:8490]"}, {"versioned_ensembl_gene_id":"ENSG00000224362.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BPG309N1.15,BAT1P2","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29988342,"end":29988738,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000223429.1","gene_symbol":"AL139156.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52162186,"end":52163026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276850.4","gene_symbol":"AC245041.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47908064,"end":47991850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000062725.9","gene_symbol":"APPBP2","gene_name":"amyloid beta precursor protein binding protein 2 [Source:HGNC Symbol;Acc:HGNC:622]","synonyms":"PAT1,KIAA0228,Hs.84084","biotype":"protein_coding","ncbi_id":"10513","summary":"The protein encoded by this gene interacts with microtubules and is functionally associated with beta-amyloid precursor protein transport and/or processing. The beta-amyloid precursor protein is a cell surface protein with signal-transducing properties, and it is thought to play a role in the pathogenesis of Alzheimer's disease. The encoded protein may be involved in regulating cell death. This gene has been found to be highly expressed in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":60443149,"end":60526219,"strand":-1,"description":"amyloid beta precursor protein binding protein 2 [Source:HGNC Symbol;Acc:HGNC:622]"}, {"versioned_ensembl_gene_id":"ENSG00000263553.1","gene_symbol":"AC022884.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24673163,"end":24674348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232244.1","gene_symbol":"BX248310.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31371102,"end":31371704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261294.1","gene_symbol":"AC120498.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1206560,"end":1207124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270093.1","gene_symbol":"AP000473.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16643529,"end":16645065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255424.1","gene_symbol":"AC027026.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19029697,"end":19030438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258358.2","gene_symbol":"AC087888.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84448625,"end":84449878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270387.1","gene_symbol":"AC115621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147916529,"end":147917386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251553.1","gene_symbol":"DDX18P4","gene_name":"DEAD-box helicase 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402222","summary":null,"start":98679402,"end":98681367,"strand":1,"description":"DEAD-box helicase 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33967]"}, {"versioned_ensembl_gene_id":"ENSG00000034239.10","gene_symbol":"EFCAB1","gene_name":"EF-hand calcium binding domain 1 [Source:HGNC Symbol;Acc:HGNC:25678]","synonyms":"FLJ11767","biotype":"protein_coding","ncbi_id":"79645","summary":null,"start":48710789,"end":48735311,"strand":-1,"description":"EF-hand calcium binding domain 1 [Source:HGNC Symbol;Acc:HGNC:25678]"}, {"versioned_ensembl_gene_id":"ENSG00000156097.12","gene_symbol":"GPR61","gene_name":"G protein-coupled receptor 61 [Source:HGNC Symbol;Acc:HGNC:13300]","synonyms":"BALGR","biotype":"protein_coding","ncbi_id":"83873","summary":"This gene belongs to the G-protein coupled receptor 1 family. G protein-coupled receptors contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. The protein encoded by this gene is most closely related to biogenic amine receptors. [provided by RefSeq, Jul 2008]","start":109539872,"end":109548406,"strand":1,"description":"G protein-coupled receptor 61 [Source:HGNC Symbol;Acc:HGNC:13300]"}, {"versioned_ensembl_gene_id":"ENSG00000169067.3","gene_symbol":"ACTBL2","gene_name":"actin, beta like 2 [Source:HGNC Symbol;Acc:HGNC:17780]","synonyms":"DKFZp686D0972","biotype":"protein_coding","ncbi_id":"345651","summary":null,"start":57480016,"end":57482809,"strand":-1,"description":"actin, beta like 2 [Source:HGNC Symbol;Acc:HGNC:17780]"}, {"versioned_ensembl_gene_id":"ENSG00000282184.2","gene_symbol":"IGHG3","gene_name":"immunoglobulin heavy constant gamma 3 (G3m marker) [Source:HGNC Symbol;Acc:HGNC:5527]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3502","summary":null,"start":105769875,"end":105772176,"strand":-1,"description":"immunoglobulin heavy constant gamma 3 (G3m marker) [Source:HGNC Symbol;Acc:HGNC:5527]"}, {"versioned_ensembl_gene_id":"ENSG00000262902.1","gene_symbol":"MTCO1P40","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52105]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075172","summary":null,"start":53105734,"end":53106358,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52105]"}, {"versioned_ensembl_gene_id":"ENSG00000254738.1","gene_symbol":"AC023078.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18956055,"end":18957015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148824.18","gene_symbol":"MTG1","gene_name":"mitochondrial ribosome associated GTPase 1 [Source:HGNC Symbol;Acc:HGNC:32159]","synonyms":"GTPBP7","biotype":"protein_coding","ncbi_id":"92170","summary":null,"start":133394094,"end":133421307,"strand":1,"description":"mitochondrial ribosome associated GTPase 1 [Source:HGNC Symbol;Acc:HGNC:32159]"}, {"versioned_ensembl_gene_id":"ENSG00000235155.4","gene_symbol":"B3GALT4","gene_name":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]","synonyms":"GalT4,beta3Gal-T4","biotype":"protein_coding","ncbi_id":"8705","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is oriented telomere to centromere in close proximity to the ribosomal protein S18 gene. The functionality of the encoded protein is limited to ganglioseries glycolipid biosynthesis. [provided by RefSeq, Jul 2008]","start":33255053,"end":33256746,"strand":1,"description":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]"}, {"versioned_ensembl_gene_id":"ENSG00000260497.1","gene_symbol":"AC141846.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47760780,"end":47760921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261231.6","gene_symbol":"LINC02133","gene_name":"long intergenic non-protein coding RNA 2133 [Source:HGNC Symbol;Acc:HGNC:52993]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927132","summary":null,"start":47724568,"end":47908431,"strand":1,"description":"long intergenic non-protein coding RNA 2133 [Source:HGNC Symbol;Acc:HGNC:52993]"}, {"versioned_ensembl_gene_id":"ENSG00000255511.1","gene_symbol":"AC023078.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18870989,"end":18873462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249135.1","gene_symbol":"AC116347.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98203059,"end":98205193,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259385.1","gene_symbol":"AC066612.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48192191,"end":48201684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255038.1","gene_symbol":"AP006287.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66067277,"end":66069619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186766.7","gene_symbol":"FOXI2","gene_name":"forkhead box I2 [Source:HGNC Symbol;Acc:HGNC:32448]","synonyms":"FLJ46831","biotype":"protein_coding","ncbi_id":"399823","summary":null,"start":127737235,"end":127741186,"strand":1,"description":"forkhead box I2 [Source:HGNC Symbol;Acc:HGNC:32448]"}, {"versioned_ensembl_gene_id":"ENSG00000254929.6","gene_symbol":"AL591684.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":47517816,"end":47553514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204172.12","gene_symbol":"AGAP9","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 9 [Source:HGNC Symbol;Acc:HGNC:23463]","synonyms":"CTGLF6,bA301J7.2,FLJ00312","biotype":"protein_coding","ncbi_id":"642517","summary":null,"start":47501854,"end":47523638,"strand":-1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 9 [Source:HGNC Symbol;Acc:HGNC:23463]"}, {"versioned_ensembl_gene_id":"ENSG00000268307.1","gene_symbol":"LINC02560","gene_name":"long intergenic non-protein coding RNA 2560 [Source:HGNC Symbol;Acc:HGNC:53600]","synonyms":"CTD-2619J13.13","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58400221,"end":58400679,"strand":1,"description":"long intergenic non-protein coding RNA 2560 [Source:HGNC Symbol;Acc:HGNC:53600]"}, {"versioned_ensembl_gene_id":"ENSG00000227011.3","gene_symbol":"C17orf112","gene_name":"chromosome 17 open reading frame 112 [Source:HGNC Symbol;Acc:HGNC:42963]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506650","summary":null,"start":52985520,"end":52987652,"strand":1,"description":"chromosome 17 open reading frame 112 [Source:HGNC Symbol;Acc:HGNC:42963]"}, {"versioned_ensembl_gene_id":"ENSG00000107263.18","gene_symbol":"RAPGEF1","gene_name":"Rap guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:4568]","synonyms":"GRF2,C3G","biotype":"protein_coding","ncbi_id":"2889","summary":"This gene encodes a human guanine nucleotide exchange factor. It transduces signals from CRK by binding the SH3 domain of CRK, and activating several members of the Ras family of GTPases. This signaling cascade that may be involved in apoptosis, integrin-mediated signal transduction, and cell transformation. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":131576770,"end":131740074,"strand":-1,"description":"Rap guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:4568]"}, {"versioned_ensembl_gene_id":"ENSG00000269855.2","gene_symbol":"RNF225","gene_name":"ring finger protein 225 [Source:HGNC Symbol;Acc:HGNC:51249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646862","summary":null,"start":58396090,"end":58397079,"strand":1,"description":"ring finger protein 225 [Source:HGNC Symbol;Acc:HGNC:51249]"}, {"versioned_ensembl_gene_id":"ENSG00000183495.13","gene_symbol":"EP400","gene_name":"E1A binding protein p400 [Source:HGNC Symbol;Acc:HGNC:11958]","synonyms":"TNRC12,P400,KIAA1818,KIAA1498,DKFZP434I225,CAGH32","biotype":"protein_coding","ncbi_id":"57634","summary":null,"start":131949920,"end":132081102,"strand":1,"description":"E1A binding protein p400 [Source:HGNC Symbol;Acc:HGNC:11958]"}, {"versioned_ensembl_gene_id":"ENSG00000170832.12","gene_symbol":"USP32","gene_name":"ubiquitin specific peptidase 32 [Source:HGNC Symbol;Acc:HGNC:19143]","synonyms":"USP10,NY-REN-60","biotype":"protein_coding","ncbi_id":"84669","summary":null,"start":60179094,"end":60422470,"strand":-1,"description":"ubiquitin specific peptidase 32 [Source:HGNC Symbol;Acc:HGNC:19143]"}, {"versioned_ensembl_gene_id":"ENSG00000175564.12","gene_symbol":"UCP3","gene_name":"uncoupling protein 3 [Source:HGNC Symbol;Acc:HGNC:12519]","synonyms":"SLC25A9","biotype":"protein_coding","ncbi_id":"7352","summary":"Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. The different UCPs have tissue-specific expression; this gene is primarily expressed in skeletal muscle. This gene's protein product is postulated to protect mitochondria against lipid-induced oxidative stress. Expression levels of this gene increase when fatty acid supplies to mitochondria exceed their oxidation capacity and the protein enables the export of fatty acids from mitochondria. UCPs contain the three solcar protein domains typically found in MACPs. Two splice variants have been found for this gene.[provided by RefSeq, Nov 2008]","start":74000281,"end":74009435,"strand":-1,"description":"uncoupling protein 3 [Source:HGNC Symbol;Acc:HGNC:12519]"}, {"versioned_ensembl_gene_id":"ENSG00000225742.5","gene_symbol":"LINC02036","gene_name":"long intergenic non-protein coding RNA 2036 [Source:HGNC Symbol;Acc:HGNC:52876]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505920","summary":null,"start":194203016,"end":194250153,"strand":-1,"description":"long intergenic non-protein coding RNA 2036 [Source:HGNC Symbol;Acc:HGNC:52876]"}, {"versioned_ensembl_gene_id":"ENSG00000240128.1","gene_symbol":"KRT18P43","gene_name":"keratin 18 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:33413]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"151825","summary":null,"start":169902980,"end":169904260,"strand":-1,"description":"keratin 18 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:33413]"}, {"versioned_ensembl_gene_id":"ENSG00000230478.1","gene_symbol":"Z96811.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87425583,"end":87425690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253688.2","gene_symbol":"AC026904.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48551527,"end":48556441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228829.1","gene_symbol":"AC005077.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76173733,"end":76177205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230001.1","gene_symbol":"AL359095.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4070906,"end":4071884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250615.1","gene_symbol":"AC008581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77073881,"end":77074520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229512.1","gene_symbol":"AC068580.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1763009,"end":1763749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229058.10","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32220356,"end":32223712,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000253955.1","gene_symbol":"AC008663.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173579643,"end":173585068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167754.12","gene_symbol":"KLK5","gene_name":"kallikrein related peptidase 5 [Source:HGNC Symbol;Acc:HGNC:6366]","synonyms":"SCTE,KLK-L2","biotype":"protein_coding","ncbi_id":"25818","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its expression is up-regulated by estrogens and progestins. The encoded protein is secreted and may be involved in desquamation in the epidermis. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":50943303,"end":50953093,"strand":-1,"description":"kallikrein related peptidase 5 [Source:HGNC Symbol;Acc:HGNC:6366]"}, {"versioned_ensembl_gene_id":"ENSG00000231487.1","gene_symbol":"AP006285.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1662584,"end":1663343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197061.4","gene_symbol":"HIST1H4C","gene_name":"histone cluster 1 H4 family member c [Source:HGNC Symbol;Acc:HGNC:4787]","synonyms":"H4/g,dJ221C16.1,H4FG","biotype":"protein_coding","ncbi_id":"8364","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26103876,"end":26104310,"strand":1,"description":"histone cluster 1 H4 family member c [Source:HGNC Symbol;Acc:HGNC:4787]"}, {"versioned_ensembl_gene_id":"ENSG00000116497.17","gene_symbol":"S100PBP","gene_name":"S100P binding protein [Source:HGNC Symbol;Acc:HGNC:25768]","synonyms":"S100PBPR,FLJ12903","biotype":"protein_coding","ncbi_id":"64766","summary":"This gene encodes a protein that was originally identified by its interaction with S100 calcium-binding protein P. Expression of this protein has been reported to be associated with pancreatic ductal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":32816767,"end":32858879,"strand":1,"description":"S100P binding protein [Source:HGNC Symbol;Acc:HGNC:25768]"}, {"versioned_ensembl_gene_id":"ENSG00000138115.13","gene_symbol":"CYP2C8","gene_name":"cytochrome P450 family 2 subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:2622]","synonyms":"CPC8","biotype":"protein_coding","ncbi_id":"1558","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital. The enzyme is known to metabolize many xenobiotics, including the anticonvulsive drug mephenytoin, benzo(a)pyrene, 7-ethyoxycoumarin, and the anti-cancer drug taxol. This gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":95036772,"end":95069497,"strand":-1,"description":"cytochrome P450 family 2 subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:2622]"}, {"versioned_ensembl_gene_id":"ENSG00000226933.1","gene_symbol":"NRBF2P2","gene_name":"nuclear receptor binding factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44605]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100114903","summary":null,"start":46023296,"end":46024156,"strand":1,"description":"nuclear receptor binding factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44605]"}, {"versioned_ensembl_gene_id":"ENSG00000258960.1","gene_symbol":"AL391261.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65900932,"end":65901451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258629.1","gene_symbol":"AL391261.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65879592,"end":65881070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249437.7","gene_symbol":"NAIP","gene_name":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]","synonyms":"NLRB1,BIRC1","biotype":"protein_coding","ncbi_id":"4671","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length; additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":70968483,"end":71025114,"strand":-1,"description":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]"}, {"versioned_ensembl_gene_id":"ENSG00000249049.1","gene_symbol":"AC074124.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91319034,"end":91325306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253654.2","gene_symbol":"AC105029.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48294026,"end":48294694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243323.7","gene_symbol":"PTPRVP","gene_name":"protein tyrosine phosphatase, receptor type V, pseudogene [Source:HGNC Symbol;Acc:HGNC:13421]","synonyms":"ESP,PTPRV,OST-PTP","biotype":"transcribed_unitary_pseudogene","ncbi_id":"148713","summary":null,"start":202168051,"end":202189455,"strand":1,"description":"protein tyrosine phosphatase, receptor type V, pseudogene [Source:HGNC Symbol;Acc:HGNC:13421]"}, {"versioned_ensembl_gene_id":"ENSG00000107223.12","gene_symbol":"EDF1","gene_name":"endothelial differentiation related factor 1 [Source:HGNC Symbol;Acc:HGNC:3164]","synonyms":"EDF-1,CFAP280","biotype":"protein_coding","ncbi_id":"8721","summary":"This gene encodes a protein that may regulate endothelial cell differentiation, lipid metabolism, and hormone-induced cardiomyocyte hypertrophy. The encoded protein has also been found to act as a transcriptional coactivator by interconnecting the general transcription factor TATA element-binding protein (TBP) and gene-specific activators. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":136862119,"end":136866286,"strand":-1,"description":"endothelial differentiation related factor 1 [Source:HGNC Symbol;Acc:HGNC:3164]"}, {"versioned_ensembl_gene_id":"ENSG00000279671.1","gene_symbol":"AC106754.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25349841,"end":25350073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257568.1","gene_symbol":"AC079035.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62482349,"end":62484932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279884.1","gene_symbol":"AC010894.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":174545385,"end":174546335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261429.2","gene_symbol":"DPPA2P4","gene_name":"developmental pluripotency associated 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44629]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131777","summary":null,"start":56686851,"end":56688052,"strand":1,"description":"developmental pluripotency associated 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44629]"}, {"versioned_ensembl_gene_id":"ENSG00000136444.9","gene_symbol":"RSAD1","gene_name":"radical S-adenosyl methionine domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25634]","synonyms":"FLJ11164","biotype":"protein_coding","ncbi_id":"55316","summary":null,"start":50478800,"end":50485975,"strand":1,"description":"radical S-adenosyl methionine domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25634]"}, {"versioned_ensembl_gene_id":"ENSG00000241155.1","gene_symbol":"ARHGAP31-AS1","gene_name":"ARHGAP31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41235]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874246","summary":null,"start":119314293,"end":119322760,"strand":-1,"description":"ARHGAP31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41235]"}, {"versioned_ensembl_gene_id":"ENSG00000242829.1","gene_symbol":"RPS26P21","gene_name":"ribosomal protein S26 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36469]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271105","summary":null,"start":119298665,"end":119299012,"strand":1,"description":"ribosomal protein S26 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36469]"}, {"versioned_ensembl_gene_id":"ENSG00000279633.1","gene_symbol":"AL137918.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61801713,"end":61803634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256172.1","gene_symbol":"LINC02420","gene_name":"long intergenic non-protein coding RNA 2420 [Source:HGNC Symbol;Acc:HGNC:53350]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724433","summary":null,"start":67440998,"end":67442559,"strand":-1,"description":"long intergenic non-protein coding RNA 2420 [Source:HGNC Symbol;Acc:HGNC:53350]"}, {"versioned_ensembl_gene_id":"ENSG00000276410.3","gene_symbol":"HIST1H2BB","gene_name":"histone cluster 1 H2B family member b [Source:HGNC Symbol;Acc:HGNC:4751]","synonyms":"H2BFF,H2B/f","biotype":"protein_coding","ncbi_id":"3018","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26043277,"end":26043657,"strand":-1,"description":"histone cluster 1 H2B family member b [Source:HGNC Symbol;Acc:HGNC:4751]"}, {"versioned_ensembl_gene_id":"ENSG00000283518.1","gene_symbol":"AL592287.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":214051194,"end":214187773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278705.1","gene_symbol":"HIST1H4B","gene_name":"histone cluster 1 H4 family member b [Source:HGNC Symbol;Acc:HGNC:4789]","synonyms":"H4FI,H4/I","biotype":"protein_coding","ncbi_id":"8366","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26026815,"end":26027252,"strand":-1,"description":"histone cluster 1 H4 family member b [Source:HGNC Symbol;Acc:HGNC:4789]"}, {"versioned_ensembl_gene_id":"ENSG00000154027.18","gene_symbol":"AK5","gene_name":"adenylate kinase 5 [Source:HGNC Symbol;Acc:HGNC:365]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26289","summary":"This gene encodes a member of the adenylate kinase family, which is involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides. This member is related to the UMP/CMP kinase of several species. It is located in the cytosol and expressed exclusively in brain. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":77282051,"end":77559969,"strand":1,"description":"adenylate kinase 5 [Source:HGNC Symbol;Acc:HGNC:365]"}, {"versioned_ensembl_gene_id":"ENSG00000238154.1","gene_symbol":"USP9YP4","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37740]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387359","summary":null,"start":9189629,"end":9204611,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37740]"}, {"versioned_ensembl_gene_id":"ENSG00000280317.1","gene_symbol":"AL732618.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":72979014,"end":72979314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228391.1","gene_symbol":"AC011995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2870558,"end":2871231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232876.1","gene_symbol":"AL353596.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135055033,"end":135060550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237720.1","gene_symbol":"AC011995.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2834264,"end":2838391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136868.10","gene_symbol":"SLC31A1","gene_name":"solute carrier family 31 member 1 [Source:HGNC Symbol;Acc:HGNC:11016]","synonyms":"hCTR1,CTR1,COPT1","biotype":"protein_coding","ncbi_id":"1317","summary":"The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011]","start":113221562,"end":113264492,"strand":1,"description":"solute carrier family 31 member 1 [Source:HGNC Symbol;Acc:HGNC:11016]"}, {"versioned_ensembl_gene_id":"ENSG00000184471.7","gene_symbol":"C1QTNF8","gene_name":"C1q and TNF related 8 [Source:HGNC Symbol;Acc:HGNC:31374]","synonyms":"UNQ5829,CTRP8","biotype":"protein_coding","ncbi_id":"390664","summary":null,"start":1090005,"end":1096244,"strand":-1,"description":"C1q and TNF related 8 [Source:HGNC Symbol;Acc:HGNC:31374]"}, {"versioned_ensembl_gene_id":"ENSG00000135773.12","gene_symbol":"CAPN9","gene_name":"calpain 9 [Source:HGNC Symbol;Acc:HGNC:1486]","synonyms":"nCL-4,GC36","biotype":"protein_coding","ncbi_id":"10753","summary":"Calpains are ubiquitous, well-conserved family of calcium-dependent, cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large subunit possesses a cysteine protease domain, and both subunits possess calcium-binding domains. Calpains have been implicated in neurodegenerative processes, as their activation can be triggered by calcium influx and oxidative stress. The protein encoded by this gene is expressed predominantly in stomach and small intestine and may have specialized functions in the digestive tract. This gene is thought to be associated with gastric cancer. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":230747384,"end":230802003,"strand":1,"description":"calpain 9 [Source:HGNC Symbol;Acc:HGNC:1486]"}, {"versioned_ensembl_gene_id":"ENSG00000122711.8","gene_symbol":"SPINK4","gene_name":"serine peptidase inhibitor, Kazal type 4 [Source:HGNC Symbol;Acc:HGNC:16646]","synonyms":"PEC-60,MGC133107","biotype":"protein_coding","ncbi_id":"27290","summary":null,"start":33218365,"end":33248567,"strand":1,"description":"serine peptidase inhibitor, Kazal type 4 [Source:HGNC Symbol;Acc:HGNC:16646]"}, {"versioned_ensembl_gene_id":"ENSG00000270427.1","gene_symbol":"NRBF2P5","gene_name":"nuclear receptor binding factor 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44683]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100118954","summary":null,"start":5776071,"end":5776858,"strand":1,"description":"nuclear receptor binding factor 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44683]"}, {"versioned_ensembl_gene_id":"ENSG00000272764.1","gene_symbol":"AL596094.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5813985,"end":5814441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205327.3","gene_symbol":"OR6C68","gene_name":"olfactory receptor family 6 subfamily C member 68 [Source:HGNC Symbol;Acc:HGNC:31297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403284","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a seven-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Mar 2014]","start":55492378,"end":55493316,"strand":1,"description":"olfactory receptor family 6 subfamily C member 68 [Source:HGNC Symbol;Acc:HGNC:31297]"}, {"versioned_ensembl_gene_id":"ENSG00000221829.9","gene_symbol":"FANCG","gene_name":"Fanconi anemia complementation group G [Source:HGNC Symbol;Acc:HGNC:3588]","synonyms":"XRCC9,FAG","biotype":"protein_coding","ncbi_id":"2189","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G. [provided by RefSeq, Jul 2008]","start":35073835,"end":35080016,"strand":-1,"description":"Fanconi anemia complementation group G [Source:HGNC Symbol;Acc:HGNC:3588]"}, {"versioned_ensembl_gene_id":"ENSG00000272459.1","gene_symbol":"AC139795.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177554824,"end":177555364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259831.1","gene_symbol":"LINC00567","gene_name":"long intergenic non-protein coding RNA 567 [Source:HGNC Symbol;Acc:HGNC:43711]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283486","summary":null,"start":110809676,"end":110813084,"strand":-1,"description":"long intergenic non-protein coding RNA 567 [Source:HGNC Symbol;Acc:HGNC:43711]"}, {"versioned_ensembl_gene_id":"ENSG00000266964.5","gene_symbol":"FXYD1","gene_name":"FXYD domain containing ion transport regulator 1 [Source:HGNC Symbol;Acc:HGNC:4025]","synonyms":"PLM","biotype":"protein_coding","ncbi_id":"5348","summary":"This gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD-domain containing ion transport regulator. Mouse FXYD5 has been termed RIC (Related to Ion Channel). FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. Transmembrane topology has been established for two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. The protein encoded by this gene is a plasma membrane substrate for several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity. Transcript variants with different 5' UTR sequences have been described in the literature. [provided by RefSeq, Jul 2008]","start":35138808,"end":35143109,"strand":1,"description":"FXYD domain containing ion transport regulator 1 [Source:HGNC Symbol;Acc:HGNC:4025]"}, {"versioned_ensembl_gene_id":"ENSG00000205358.3","gene_symbol":"MT1H","gene_name":"metallothionein 1H [Source:HGNC Symbol;Acc:HGNC:7400]","synonyms":"MT1","biotype":"protein_coding","ncbi_id":"4496","summary":null,"start":56669814,"end":56671129,"strand":1,"description":"metallothionein 1H [Source:HGNC Symbol;Acc:HGNC:7400]"}, {"versioned_ensembl_gene_id":"ENSG00000244144.1","gene_symbol":"AC128688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112185480,"end":112185998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170074.19","gene_symbol":"FAM153A","gene_name":"family with sequence similarity 153 member A [Source:HGNC Symbol;Acc:HGNC:29940]","synonyms":"NY-REN-7","biotype":"protein_coding","ncbi_id":"285596","summary":null,"start":177707981,"end":177783398,"strand":-1,"description":"family with sequence similarity 153 member A [Source:HGNC Symbol;Acc:HGNC:29940]"}, {"versioned_ensembl_gene_id":"ENSG00000253519.1","gene_symbol":"AC106801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157565964,"end":157569098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219188.1","gene_symbol":"CACYBPP3","gene_name":"calcyclin binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45124]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480809","summary":null,"start":158515605,"end":158516229,"strand":-1,"description":"calcyclin binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45124]"}, {"versioned_ensembl_gene_id":"ENSG00000142515.14","gene_symbol":"KLK3","gene_name":"kallikrein related peptidase 3 [Source:HGNC Symbol;Acc:HGNC:6364]","synonyms":"PSA,APS","biotype":"protein_coding","ncbi_id":"354","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. The gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. It encodes a single-chain glycoprotein, a protease which is synthesized in the epithelial cells of the prostate gland, and is present in seminal plasma. It is thought to function normally in the liquefaction of seminal coagulum, presumably by hydrolysis of the high molecular mass seminal vesicle protein. The serum level of this protein, called PSA in the clinical setting, is useful in the diagnosis and monitoring of prostatic carcinoma. Alternate splicing of this gene generates several transcript variants encoding different isoforms. [provided by RefSeq, Dec 2019]","start":50854915,"end":50860764,"strand":1,"description":"kallikrein related peptidase 3 [Source:HGNC Symbol;Acc:HGNC:6364]"}, {"versioned_ensembl_gene_id":"ENSG00000246596.6","gene_symbol":"AC139795.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":177619059,"end":177672209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172139.14","gene_symbol":"SLC9C1","gene_name":"solute carrier family 9 member C1 [Source:HGNC Symbol;Acc:HGNC:31401]","synonyms":"SLC9A10,NHE","biotype":"protein_coding","ncbi_id":"285335","summary":"SLC9A10 is a member of the sodium-hydrogen exchanger (NHE) family (see SLC9A1, MIM 107310) and is required for male fertility and sperm motility (Wang et al., 2003 [PubMed 14634667]).[supplied by OMIM, Apr 2009]","start":112140887,"end":112294258,"strand":-1,"description":"solute carrier family 9 member C1 [Source:HGNC Symbol;Acc:HGNC:31401]"}, {"versioned_ensembl_gene_id":"ENSG00000213695.3","gene_symbol":"RPS7P14","gene_name":"ribosomal protein S7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36602]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646108","summary":null,"start":74409518,"end":74410100,"strand":1,"description":"ribosomal protein S7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36602]"}, {"versioned_ensembl_gene_id":"ENSG00000223390.1","gene_symbol":"AL445685.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52033391,"end":52044279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203408.4","gene_symbol":"OR6C71P","gene_name":"olfactory receptor family 6 subfamily C member 71 pseudogene [Source:HGNC Symbol;Acc:HGNC:31300]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390324","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55376742,"end":55378797,"strand":-1,"description":"olfactory receptor family 6 subfamily C member 71 pseudogene [Source:HGNC Symbol;Acc:HGNC:31300]"}, {"versioned_ensembl_gene_id":"ENSG00000168703.5","gene_symbol":"WFDC12","gene_name":"WAP four-disulfide core domain 12 [Source:HGNC Symbol;Acc:HGNC:16115]","synonyms":"WAP2,dJ211D12.4,C20orf122","biotype":"protein_coding","ncbi_id":"128488","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. [provided by RefSeq, Jul 2008]","start":45123425,"end":45124465,"strand":-1,"description":"WAP four-disulfide core domain 12 [Source:HGNC Symbol;Acc:HGNC:16115]"}, {"versioned_ensembl_gene_id":"ENSG00000281622.1","gene_symbol":"AC020679.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21534392,"end":21535271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225454.2","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":30922062,"end":30922884,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000253740.5","gene_symbol":"AP001205.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100618581,"end":100619993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037241.7","gene_symbol":"RPL26L1","gene_name":"ribosomal protein L26 like 1 [Source:HGNC Symbol;Acc:HGNC:17050]","synonyms":"RPL26P1","biotype":"protein_coding","ncbi_id":"51121","summary":"This gene encodes a protein that shares high sequence similarity with ribosomal protein L26. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Dec 2015]","start":172958729,"end":172969771,"strand":1,"description":"ribosomal protein L26 like 1 [Source:HGNC Symbol;Acc:HGNC:17050]"}, {"versioned_ensembl_gene_id":"ENSG00000183421.11","gene_symbol":"RIPK4","gene_name":"receptor interacting serine/threonine kinase 4 [Source:HGNC Symbol;Acc:HGNC:496]","synonyms":"DIK,ANKRD3,ANKK2,RIP4,PKK","biotype":"protein_coding","ncbi_id":"54101","summary":"The protein encoded by this gene is a serine/threonine protein kinase that interacts with protein kinase C-delta. The encoded protein can also activate NFkappaB and is required for keratinocyte differentiation. This kinase undergoes autophosphorylation. [provided by RefSeq, Jul 2008]","start":41739369,"end":41767106,"strand":-1,"description":"receptor interacting serine/threonine kinase 4 [Source:HGNC Symbol;Acc:HGNC:496]"}, {"versioned_ensembl_gene_id":"ENSG00000115827.13","gene_symbol":"DCAF17","gene_name":"DDB1 and CUL4 associated factor 17 [Source:HGNC Symbol;Acc:HGNC:25784]","synonyms":"FLJ13096,C2orf37","biotype":"protein_coding","ncbi_id":"80067","summary":"This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":171434217,"end":171485052,"strand":1,"description":"DDB1 and CUL4 associated factor 17 [Source:HGNC Symbol;Acc:HGNC:25784]"}, {"versioned_ensembl_gene_id":"ENSG00000114812.12","gene_symbol":"VIPR1","gene_name":"vasoactive intestinal peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:12694]","synonyms":"VPAC1R,VPAC1,RDC1,HVR1","biotype":"protein_coding","ncbi_id":"7433","summary":"This gene encodes a receptor for vasoactive intestinal peptide, a small neuropeptide. Vasoactive intestinal peptide is involved in smooth muscle relaxation, exocrine and endocrine secretion, and water and ion flux in lung and intestinal epithelia. Its actions are effected through integral membrane receptors associated with a guanine nucleotide binding protein which activates adenylate cyclase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":42489299,"end":42537573,"strand":1,"description":"vasoactive intestinal peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:12694]"}, {"versioned_ensembl_gene_id":"ENSG00000197620.10","gene_symbol":"CXorf40A","gene_name":"chromosome X open reading frame 40A [Source:HGNC Symbol;Acc:HGNC:28089]","synonyms":"EOLA1,CXorf40","biotype":"protein_coding","ncbi_id":"91966","summary":null,"start":149540355,"end":149550510,"strand":1,"description":"chromosome X open reading frame 40A [Source:HGNC Symbol;Acc:HGNC:28089]"}, {"versioned_ensembl_gene_id":"ENSG00000229894.4","gene_symbol":"GK3P","gene_name":"glycerol kinase 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4292]","synonyms":"GKTB,GKP3","biotype":"protein_coding","ncbi_id":"2713","summary":null,"start":165277812,"end":165279679,"strand":-1,"description":"glycerol kinase 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4292]"}, {"versioned_ensembl_gene_id":"ENSG00000238245.2","gene_symbol":"MYO5BP2","gene_name":"myosin VB pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392335","summary":null,"start":62857208,"end":62858484,"strand":1,"description":"myosin VB pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38496]"}, {"versioned_ensembl_gene_id":"ENSG00000204490.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31562973,"end":31565742,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000167748.10","gene_symbol":"KLK1","gene_name":"kallikrein 1 [Source:HGNC Symbol;Acc:HGNC:6357]","synonyms":"Klk6","biotype":"protein_coding","ncbi_id":"3816","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. This protein is functionally conserved in its capacity to release the vasoactive peptide, Lys-bradykinin, from low molecular weight kininogen. [provided by RefSeq, Jul 2008]","start":50819148,"end":50823787,"strand":-1,"description":"kallikrein 1 [Source:HGNC Symbol;Acc:HGNC:6357]"}, {"versioned_ensembl_gene_id":"ENSG00000219693.3","gene_symbol":"FGF7P8","gene_name":"fibroblast growth factor 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:34516]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100113421","summary":null,"start":62888535,"end":62889921,"strand":1,"description":"fibroblast growth factor 7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:34516]"}, {"versioned_ensembl_gene_id":"ENSG00000225316.1","gene_symbol":"LINC00350","gene_name":"long intergenic non-protein coding RNA 350 [Source:HGNC Symbol;Acc:HGNC:42668]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874136","summary":null,"start":19587118,"end":19588350,"strand":1,"description":"long intergenic non-protein coding RNA 350 [Source:HGNC Symbol;Acc:HGNC:42668]"}, {"versioned_ensembl_gene_id":"ENSG00000112640.14","gene_symbol":"PPP2R5D","gene_name":"protein phosphatase 2 regulatory subunit B'delta [Source:HGNC Symbol;Acc:HGNC:9312]","synonyms":"B56delta,B56D","biotype":"protein_coding","ncbi_id":"5528","summary":"The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a delta isoform of the regulatory subunit B56 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":42984499,"end":43012342,"strand":1,"description":"protein phosphatase 2 regulatory subunit B'delta [Source:HGNC Symbol;Acc:HGNC:9312]"}, {"versioned_ensembl_gene_id":"ENSG00000238130.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31559460,"end":31561730,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000225233.1","gene_symbol":"AL592402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":213492301,"end":213546447,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270243.1","gene_symbol":"AC022217.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172785262,"end":172785424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223881.1","gene_symbol":"AL157402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198597724,"end":198598868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246214.1","gene_symbol":"AC022113.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16615926,"end":16629969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086159.12","gene_symbol":"AQP6","gene_name":"aquaporin 6 [Source:HGNC Symbol;Acc:HGNC:639]","synonyms":"AQP2L","biotype":"protein_coding","ncbi_id":"363","summary":"The protein encoded by this gene is an aquaporin protein, which functions as a water channel in cells. Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein (MIP or AQP0). This protein is specific for the kidney. This gene and related family members AQP0, AQP2, and AQP5 reside in a cluster on chromosome 12q13. [provided by RefSeq, Jul 2008]","start":49967194,"end":49977139,"strand":1,"description":"aquaporin 6 [Source:HGNC Symbol;Acc:HGNC:639]"}, {"versioned_ensembl_gene_id":"ENSG00000110080.18","gene_symbol":"ST3GAL4","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:10864]","synonyms":"STZ,SIAT4C,SIAT4,SAT3,NANTA3,FLJ11867,CGS23","biotype":"protein_coding","ncbi_id":"6484","summary":"This gene encodes a member of the glycosyltransferase 29 family, a group of enzymes involved in protein glycosylation. The encoded protein is targeted to Golgi membranes but may be proteolytically processed and secreted. The gene product may also be involved in the increased expression of sialyl Lewis X antigen seen in inflammatory responses. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":126355640,"end":126440344,"strand":1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:10864]"}, {"versioned_ensembl_gene_id":"ENSG00000122068.12","gene_symbol":"FYTTD1","gene_name":"forty-two-three domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25407]","synonyms":"UIF,DKFZp761B1514","biotype":"protein_coding","ncbi_id":"84248","summary":null,"start":197737179,"end":197787596,"strand":1,"description":"forty-two-three domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25407]"}, {"versioned_ensembl_gene_id":"ENSG00000196460.12","gene_symbol":"RFX8","gene_name":"RFX family member 8, lacking RFX DNA binding domain [Source:HGNC Symbol;Acc:HGNC:37253]","synonyms":"FLJ42986","biotype":"protein_coding","ncbi_id":"731220","summary":null,"start":101397361,"end":101474703,"strand":-1,"description":"RFX family member 8, lacking RFX DNA binding domain [Source:HGNC Symbol;Acc:HGNC:37253]"}, {"versioned_ensembl_gene_id":"ENSG00000197714.8","gene_symbol":"ZNF460","gene_name":"zinc finger protein 460 [Source:HGNC Symbol;Acc:HGNC:21628]","synonyms":"ZNF272,HZF8","biotype":"protein_coding","ncbi_id":"10794","summary":"Zinc finger proteins, such as ZNF272, interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, May 2004]","start":57280051,"end":57293569,"strand":1,"description":"zinc finger protein 460 [Source:HGNC Symbol;Acc:HGNC:21628]"}, {"versioned_ensembl_gene_id":"ENSG00000114388.12","gene_symbol":"NPRL2","gene_name":"NPR2 like, GATOR1 complex subunit [Source:HGNC Symbol;Acc:HGNC:24969]","synonyms":"TUSC4,NPR2L,NPR2","biotype":"protein_coding","ncbi_id":"10641","summary":null,"start":50347330,"end":50351091,"strand":-1,"description":"NPR2 like, GATOR1 complex subunit [Source:HGNC Symbol;Acc:HGNC:24969]"}, {"versioned_ensembl_gene_id":"ENSG00000043355.11","gene_symbol":"ZIC2","gene_name":"Zic family member 2 [Source:HGNC Symbol;Acc:HGNC:12873]","synonyms":"HPE5","biotype":"protein_coding","ncbi_id":"7546","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This protein functions as a transcriptional repressor and may regulate tissue specific expression of dopamine receptor D1. Expansion of an alanine repeat in the C-terminus of the encoded protein and other mutations in this gene cause holoprosencephaly type 5. Holoprosencephaly is the most common structural anomaly of the human brain. A polyhistidine tract polymorphism in this gene may be associated with increased risk of neural tube defects. This gene is closely linked to a gene encoding zinc finger protein of the cerebellum 5, a related family member on chromosome 13. [provided by RefSeq, Jul 2016]","start":99981772,"end":99986773,"strand":1,"description":"Zic family member 2 [Source:HGNC Symbol;Acc:HGNC:12873]"}, {"versioned_ensembl_gene_id":"ENSG00000274116.1","gene_symbol":"AC090132.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83293925,"end":83294271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109689.15","gene_symbol":"STIM2","gene_name":"stromal interaction molecule 2 [Source:HGNC Symbol;Acc:HGNC:19205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57620","summary":"This gene is a member of the stromal interaction molecule (STIM) family and likely arose, along with related family member STIM1, from a common ancestral gene. The encoded protein functions to regulate calcium concentrations in the cytosol and endoplasmic reticulum, and is involved in the activation of plasma membrane Orai Ca(2+) entry channels. This gene initiates translation from a non-AUG (UUG) start site. A signal peptide is cleaved from the resulting protein. Multiple transcript variants result from alternative splicing. [provided by RefSeq, Dec 2009]","start":26857678,"end":27025381,"strand":1,"description":"stromal interaction molecule 2 [Source:HGNC Symbol;Acc:HGNC:19205]"}, {"versioned_ensembl_gene_id":"ENSG00000137841.11","gene_symbol":"PLCB2","gene_name":"phospholipase C beta 2 [Source:HGNC Symbol;Acc:HGNC:9055]","synonyms":"FLJ38135","biotype":"protein_coding","ncbi_id":"5330","summary":"The protein encoded by this gene is a phosphodiesterase that catalyzes the hydrolysis of phosphatidylinositol 4,5-bisphosphate to the second messengers inositol 1,4,5-trisphosphate (IP3) and diacylglycerol. The encoded protein is activated by G proteins and has been shown to be involved in the type 2 taste receptor signal transduction pathway. In addition, nuclear factor kappa B can regulate the transcription of this gene, whose protein product is also an important regulator of platelet responses. [provided by RefSeq, Jan 2017]","start":40278176,"end":40307935,"strand":-1,"description":"phospholipase C beta 2 [Source:HGNC Symbol;Acc:HGNC:9055]"}, {"versioned_ensembl_gene_id":"ENSG00000230134.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33122692,"end":33125676,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000157911.9","gene_symbol":"PEX10","gene_name":"peroxisomal biogenesis factor 10 [Source:HGNC Symbol;Acc:HGNC:8851]","synonyms":"RNF69","biotype":"protein_coding","ncbi_id":"5192","summary":"This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":2403964,"end":2413797,"strand":-1,"description":"peroxisomal biogenesis factor 10 [Source:HGNC Symbol;Acc:HGNC:8851]"}, {"versioned_ensembl_gene_id":"ENSG00000137310.11","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31158542,"end":31167159,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000223696.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33109121,"end":33121230,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000280156.1","gene_symbol":"AC006548.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":16950086,"end":17034417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229177.1","gene_symbol":"AC008154.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134346071,"end":134350791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160401.14","gene_symbol":"CFAP157","gene_name":"cilia and flagella associated protein 157 [Source:HGNC Symbol;Acc:HGNC:27843]","synonyms":"C9orf117","biotype":"protein_coding","ncbi_id":"286207","summary":null,"start":127706989,"end":127716002,"strand":1,"description":"cilia and flagella associated protein 157 [Source:HGNC Symbol;Acc:HGNC:27843]"}, {"versioned_ensembl_gene_id":"ENSG00000227528.5","gene_symbol":"DIAPH3-AS1","gene_name":"DIAPH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39915]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874195","summary":null,"start":60012751,"end":60044357,"strand":1,"description":"DIAPH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39915]"}, {"versioned_ensembl_gene_id":"ENSG00000281966.1","gene_symbol":"IGHV3-76","gene_name":"immunoglobulin heavy variable 3-76 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5626]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28406","summary":null,"start":106852045,"end":106852339,"strand":-1,"description":"immunoglobulin heavy variable 3-76 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5626]"}, {"versioned_ensembl_gene_id":"ENSG00000145703.15","gene_symbol":"IQGAP2","gene_name":"IQ motif containing GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:6111]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10788","summary":"This gene encodes a member of the IQGAP family. The encoded protein contains three IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. This protein interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. It also acts as a tumor suppressor and has been found to play a role in regulating innate antiviral responses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":76403249,"end":76708132,"strand":1,"description":"IQ motif containing GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:6111]"}, {"versioned_ensembl_gene_id":"ENSG00000237105.2","gene_symbol":"HCP5","gene_name":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]","synonyms":"P5-1,D6S2650E","biotype":"processed_transcript","ncbi_id":"10866","summary":null,"start":31450619,"end":31453253,"strand":1,"description":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]"}, {"versioned_ensembl_gene_id":"ENSG00000223608.1","gene_symbol":"DSCR4-IT1","gene_name":"DSCR4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41328]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874327","summary":null,"start":38006544,"end":38010618,"strand":-1,"description":"DSCR4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41328]"}, {"versioned_ensembl_gene_id":"ENSG00000131864.10","gene_symbol":"USP29","gene_name":"ubiquitin specific peptidase 29 [Source:HGNC Symbol;Acc:HGNC:18563]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57663","summary":null,"start":57119138,"end":57131926,"strand":1,"description":"ubiquitin specific peptidase 29 [Source:HGNC Symbol;Acc:HGNC:18563]"}, {"versioned_ensembl_gene_id":"ENSG00000266988.5","gene_symbol":"AC021517.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45483345,"end":45529855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121064.12","gene_symbol":"SCPEP1","gene_name":"serine carboxypeptidase 1 [Source:HGNC Symbol;Acc:HGNC:29507]","synonyms":"RISC","biotype":"protein_coding","ncbi_id":"59342","summary":null,"start":56978105,"end":57006768,"strand":1,"description":"serine carboxypeptidase 1 [Source:HGNC Symbol;Acc:HGNC:29507]"}, {"versioned_ensembl_gene_id":"ENSG00000204241.7","gene_symbol":"AP000911.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134032272,"end":134046849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100241.20","gene_symbol":"SBF1","gene_name":"SET binding factor 1 [Source:HGNC Symbol;Acc:HGNC:10542]","synonyms":"MTMR5,DENND7A","biotype":"protein_coding","ncbi_id":"6305","summary":"This gene encodes a member of the protein-tyrosine phosphatase family. However, the encoded protein does not appear to be a catalytically active phosphatase because it lacks several amino acids in the catalytic pocket. This protein contains a Guanine nucleotide exchange factor (GEF) domain which is necessary for its role in growth and differentiation. Mutations in this gene have been associated with Charcot-Marie-Tooth disease 4B3. Pseudogenes of this gene have been defined on chromosomes 1 and 8. [provided by RefSeq, Dec 2014]","start":50445000,"end":50475024,"strand":-1,"description":"SET binding factor 1 [Source:HGNC Symbol;Acc:HGNC:10542]"}, {"versioned_ensembl_gene_id":"ENSG00000105246.5","gene_symbol":"EBI3","gene_name":"Epstein-Barr virus induced 3 [Source:HGNC Symbol;Acc:HGNC:3129]","synonyms":"IL35B,IL27B","biotype":"protein_coding","ncbi_id":"10148","summary":"This gene was identified by its induced expression in B lymphocytes in response Epstein-Barr virus infection. It encodes a secreted glycoprotein belonging to the hematopoietin receptor family, and heterodimerizes with a 28 kDa protein to form interleukin 27 (IL-27). IL-27 regulates T cell and inflammatory responses, in part by activating the Jak/STAT pathway of CD4+ T cells. [provided by RefSeq, Sep 2008]","start":4229498,"end":4237531,"strand":1,"description":"Epstein-Barr virus induced 3 [Source:HGNC Symbol;Acc:HGNC:3129]"}, {"versioned_ensembl_gene_id":"ENSG00000255406.1","gene_symbol":"AP000911.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134026987,"end":134028118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229087.1","gene_symbol":"AC007738.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15397435,"end":15397782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205041.1","gene_symbol":"AC118344.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40273489,"end":40275479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243607.3","gene_symbol":"AP001318.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126278257,"end":126278577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211715.1","gene_symbol":"TRBV5-3","gene_name":"T-cell receptor beta variable 5-3 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12220]","synonyms":"TRBV53,TCRBV5S5P,TCRBV5S3","biotype":"TR_V_gene","ncbi_id":"28612","summary":null,"start":142389202,"end":142389668,"strand":1,"description":"T-cell receptor beta variable 5-3 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12220]"}, {"versioned_ensembl_gene_id":"ENSG00000278975.1","gene_symbol":"AC007012.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6703883,"end":6705558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228957.1","gene_symbol":"AL512590.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97386240,"end":97396112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257780.5","gene_symbol":"GLYCAM1","gene_name":"glycosylation dependent cell adhesion molecule 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18023]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"644076","summary":null,"start":54608187,"end":54610462,"strand":-1,"description":"glycosylation dependent cell adhesion molecule 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18023]"}, {"versioned_ensembl_gene_id":"ENSG00000276810.1","gene_symbol":"AC244093.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37162616,"end":37163139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258540.1","gene_symbol":"AC107958.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91676771,"end":91677060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240508.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32877612,"end":32913027,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000233213.1","gene_symbol":"KCNJ6-AS1","gene_name":"KCNJ6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41352]","synonyms":"KCNJ6-IT1","biotype":"sense_intronic","ncbi_id":"105372799","summary":null,"start":37717102,"end":37719569,"strand":-1,"description":"KCNJ6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41352]"}, {"versioned_ensembl_gene_id":"ENSG00000258954.1","gene_symbol":"AC107958.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91532891,"end":91535095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275539.5","gene_symbol":"LILRA6","gene_name":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]","synonyms":"CD85b,LILRB6,ILT8","biotype":"protein_coding","ncbi_id":"79168","summary":null,"start":54239108,"end":54243457,"strand":-1,"description":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]"}, {"versioned_ensembl_gene_id":"ENSG00000068383.18","gene_symbol":"INPP5A","gene_name":"inositol polyphosphate-5-phosphatase A [Source:HGNC Symbol;Acc:HGNC:6076]","synonyms":"5PTASE","biotype":"protein_coding","ncbi_id":"3632","summary":"The protein encoded by this gene is a membrane-associated type I inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. [provided by RefSeq, Jul 2008]","start":132537820,"end":132783480,"strand":1,"description":"inositol polyphosphate-5-phosphatase A [Source:HGNC Symbol;Acc:HGNC:6076]"}, {"versioned_ensembl_gene_id":"ENSG00000254896.1","gene_symbol":"OPCML-IT1","gene_name":"OPCML intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41366]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874333","summary":null,"start":133360029,"end":133366080,"strand":-1,"description":"OPCML intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41366]"}, {"versioned_ensembl_gene_id":"ENSG00000279711.1","gene_symbol":"AP004782.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133064697,"end":133068129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237617.1","gene_symbol":"AC013410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173705948,"end":173706148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254533.1","gene_symbol":"AF186192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144698614,"end":144699185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227745.1","gene_symbol":"AC098826.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":132132856,"end":132139429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226886.1","gene_symbol":"AC093787.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132037787,"end":132037993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270632.1","gene_symbol":"AL356575.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100198187,"end":100198469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265115.1","gene_symbol":"AC011824.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33627027,"end":33635057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249332.1","gene_symbol":"AC016651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15112377,"end":15117007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226049.3","gene_symbol":"AC123769.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34036681,"end":34039872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233311.1","gene_symbol":"MTCO1P54","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:52119]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075178","summary":null,"start":202619185,"end":202619896,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:52119]"}, {"versioned_ensembl_gene_id":"ENSG00000078902.15","gene_symbol":"TOLLIP","gene_name":"toll interacting protein [Source:HGNC Symbol;Acc:HGNC:16476]","synonyms":"IL-1RAcPIP","biotype":"protein_coding","ncbi_id":"54472","summary":"This gene encodes a ubiquitin-binding protein that interacts with several Toll-like receptor (TLR) signaling cascade components. The encoded protein regulates inflammatory signaling and is involved in interleukin-1 receptor trafficking and in the turnover of IL1R-associated kinase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":1274371,"end":1309654,"strand":-1,"description":"toll interacting protein [Source:HGNC Symbol;Acc:HGNC:16476]"}, {"versioned_ensembl_gene_id":"ENSG00000236915.1","gene_symbol":"AL356270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86571181,"end":86693203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175198.15","gene_symbol":"PCCA","gene_name":"propionyl-CoA carboxylase alpha subunit [Source:HGNC Symbol;Acc:HGNC:8653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5095","summary":"The protein encoded by this gene is the alpha subunit of the heterodimeric mitochondrial enzyme Propionyl-CoA carboxylase. PCCA encodes the biotin-binding region of this enzyme. Mutations in either PCCA or PCCB (encoding the beta subunit) lead to an enzyme deficiency resulting in propionic acidemia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":100089015,"end":100530437,"strand":1,"description":"propionyl-CoA carboxylase alpha subunit [Source:HGNC Symbol;Acc:HGNC:8653]"}, {"versioned_ensembl_gene_id":"ENSG00000229061.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30617079,"end":30637059,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000261209.1","gene_symbol":"SULT1C2P2","gene_name":"sulfotransferase family, cytosolic, 1C, member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51595]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480333","summary":null,"start":108317725,"end":108318611,"strand":1,"description":"sulfotransferase family, cytosolic, 1C, member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51595]"}, {"versioned_ensembl_gene_id":"ENSG00000236279.6","gene_symbol":"CLEC2L","gene_name":"C-type lectin domain family 2 member L [Source:HGNC Symbol;Acc:HGNC:21969]","synonyms":"FLJ32986","biotype":"protein_coding","ncbi_id":"154790","summary":null,"start":139523856,"end":139544984,"strand":1,"description":"C-type lectin domain family 2 member L [Source:HGNC Symbol;Acc:HGNC:21969]"}, {"versioned_ensembl_gene_id":"ENSG00000151414.14","gene_symbol":"NEK7","gene_name":"NIMA related kinase 7 [Source:HGNC Symbol;Acc:HGNC:13386]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140609","summary":"NIMA-related kinases share high amino acid sequence identity with the gene product of the Aspergillus nidulans 'never in mitosis A' gene, which controls initiation of mitosis.[supplied by OMIM, Jul 2002]","start":198156963,"end":198322420,"strand":1,"description":"NIMA related kinase 7 [Source:HGNC Symbol;Acc:HGNC:13386]"}, {"versioned_ensembl_gene_id":"ENSG00000153923.10","gene_symbol":"CLCA3P","gene_name":"chloride channel accessory 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2017]","synonyms":"CLCA3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"9629","summary":"This gene is a transcribed pseudogene belonging to the calcium sensitive chloride conductance protein family. To date, all members of this gene family map to the same site on chromosome 1p31-p22 and share high degrees of homology in size, sequence and predicted structure, but differ significantly in their tissue distributions. This gene contains several nonsense codons compared to other family members that render the transcript a candidate for nonsense-mediated mRNA decay (NMD). Therefore, this gene is unlikely to be protein-coding. [provided by RefSeq, Jan 2009]","start":86634273,"end":86655376,"strand":1,"description":"chloride channel accessory 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:2017]"}, {"versioned_ensembl_gene_id":"ENSG00000251623.1","gene_symbol":"AC139491.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176137157,"end":176155738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253183.1","gene_symbol":"AC005531.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139502453,"end":139503812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255456.1","gene_symbol":"AC084125.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144584040,"end":144586488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147799.11","gene_symbol":"ARHGAP39","gene_name":"Rho GTPase activating protein 39 [Source:HGNC Symbol;Acc:HGNC:29351]","synonyms":"Vilse,KIAA1688,CrGAP","biotype":"protein_coding","ncbi_id":"80728","summary":null,"start":144529179,"end":144605816,"strand":-1,"description":"Rho GTPase activating protein 39 [Source:HGNC Symbol;Acc:HGNC:29351]"}, {"versioned_ensembl_gene_id":"ENSG00000277050.1","gene_symbol":"AL122125.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51637348,"end":51637947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223727.6","gene_symbol":"AC034195.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3250687,"end":3627296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267510.1","gene_symbol":"AC011451.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9291515,"end":9294482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255125.1","gene_symbol":"AC116535.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10783313,"end":10801625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239819.2","gene_symbol":"IGKV1D-8","gene_name":"immunoglobulin kappa variable 1D-8 [Source:HGNC Symbol;Acc:HGNC:5759]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28904","summary":null,"start":90220727,"end":90221384,"strand":1,"description":"immunoglobulin kappa variable 1D-8 [Source:HGNC Symbol;Acc:HGNC:5759]"}, {"versioned_ensembl_gene_id":"ENSG00000229487.1","gene_symbol":"ALG13-AS1","gene_name":"ALG13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41277]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478971","summary":null,"start":111706649,"end":111711101,"strand":-1,"description":"ALG13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41277]"}, {"versioned_ensembl_gene_id":"ENSG00000277796.2","gene_symbol":"CCL3L1","gene_name":"C-C motif chemokine ligand 3 like 1 [Source:HGNC Symbol;Acc:HGNC:10628]","synonyms":"LD78BETA,G0S19-2,D17S1718,SCYA3L1,SCYA3L","biotype":"protein_coding","ncbi_id":"6349","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this gene binds to several chemokine receptors, including chemokine binding protein 2 and chemokine (C-C motif) receptor 5 (CCR5). CCR5 is a co-receptor for HIV, and binding of this protein to CCR5 inhibits HIV entry. The copy number of this gene varies among individuals, where most individuals have one to six copies, and a minority of individuals have zero or more than six copies. There are conflicting reports about copy number variation of this gene and its correlation to disease susceptibility. This record represents one of two copies that are present on the ALT_REF_LOCI_2 alternate haplotype of the GRCh38 human reference genome assembly. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36194906,"end":36196795,"strand":-1,"description":"C-C motif chemokine ligand 3 like 1 [Source:HGNC Symbol;Acc:HGNC:10628]"}, {"versioned_ensembl_gene_id":"ENSG00000250348.1","gene_symbol":"AC113404.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76285542,"end":76311462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281016.1","gene_symbol":"AC092574.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":386174,"end":454070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235211.4","gene_symbol":"TMSB10P2","gene_name":"thymosin beta 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41950]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873786","summary":null,"start":18341216,"end":18341346,"strand":1,"description":"thymosin beta 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41950]"}, {"versioned_ensembl_gene_id":"ENSG00000282586.1","gene_symbol":"IGHV3-60","gene_name":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28417","summary":null,"start":106655878,"end":106656334,"strand":-1,"description":"immunoglobulin heavy variable 3-60 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5614]"}, {"versioned_ensembl_gene_id":"ENSG00000274730.1","gene_symbol":"AC141273.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20618205,"end":20620758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260510.1","gene_symbol":"AC004381.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20743663,"end":20766620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227305.1","gene_symbol":"AC073188.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63393788,"end":63422046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234387.1","gene_symbol":"AC073188.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63394277,"end":63395439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110074.10","gene_symbol":"FOXRED1","gene_name":"FAD dependent oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26927]","synonyms":"H17","biotype":"protein_coding","ncbi_id":"55572","summary":"This gene encodes a protein that contains a FAD-dependent oxidoreductase domain. The encoded protein is localized to the mitochondria and may function as a chaperone protein required for the function of mitochondrial complex I. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]","start":126269055,"end":126278131,"strand":1,"description":"FAD dependent oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26927]"}, {"versioned_ensembl_gene_id":"ENSG00000155636.14","gene_symbol":"RBM45","gene_name":"RNA binding motif protein 45 [Source:HGNC Symbol;Acc:HGNC:24468]","synonyms":"FLJ44612,DRB1","biotype":"protein_coding","ncbi_id":"129831","summary":"This gene encodes a member of the RNA recognition motif (RRM)-type RNA-binding family of proteins. This protein exhibits preferential binding to poly(C) RNA. Initial cloning of this gene found that the rat ortholog was dynamically expressed in the developing rat brain. This protein has been localized to inclusion bodies in the brain and spinal cord of amyotrophic lateral sclerosis and Alzheimer's patients. A pseudogene has been identified on chromosome 8. [provided by RefSeq, Feb 2015]","start":178112424,"end":178139011,"strand":1,"description":"RNA binding motif protein 45 [Source:HGNC Symbol;Acc:HGNC:24468]"}, {"versioned_ensembl_gene_id":"ENSG00000230891.6","gene_symbol":"LINC00692","gene_name":"long intergenic non-protein coding RNA 692 [Source:HGNC Symbol;Acc:HGNC:27708]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285326","summary":null,"start":25858533,"end":25873700,"strand":-1,"description":"long intergenic non-protein coding RNA 692 [Source:HGNC Symbol;Acc:HGNC:27708]"}, {"versioned_ensembl_gene_id":"ENSG00000179134.15","gene_symbol":"SAMD4B","gene_name":"sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:25492]","synonyms":"SMGB,MGC99832,hSmaug2,FLJ10211","biotype":"protein_coding","ncbi_id":"55095","summary":null,"start":39342396,"end":39385710,"strand":1,"description":"sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:25492]"}, {"versioned_ensembl_gene_id":"ENSG00000104497.13","gene_symbol":"SNX16","gene_name":"sorting nexin 16 [Source:HGNC Symbol;Acc:HGNC:14980]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64089","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. The protein encoded by this gene associates with late endosome membranes as is involved in tubule formation, cholesterol transport, and transport of tetraspanin CD81. The encoded protein also inhibits cell migration and tumorigenesis. [provided by RefSeq, Jan 2017]","start":81799581,"end":81842866,"strand":-1,"description":"sorting nexin 16 [Source:HGNC Symbol;Acc:HGNC:14980]"}, {"versioned_ensembl_gene_id":"ENSG00000282713.1","gene_symbol":"AC098965.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17040606,"end":17041572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136271.10","gene_symbol":"DDX56","gene_name":"DEAD-box helicase 56 [Source:HGNC Symbol;Acc:HGNC:18193]","synonyms":"NOH61","biotype":"protein_coding","ncbi_id":"54606","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene shows ATPase activity in the presence of polynucleotides and associates with nucleoplasmic 65S preribosomal particles. This gene may be involved in ribosome synthesis, most likely during assembly of the large 60S ribosomal subunit. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":44565417,"end":44575051,"strand":-1,"description":"DEAD-box helicase 56 [Source:HGNC Symbol;Acc:HGNC:18193]"}, {"versioned_ensembl_gene_id":"ENSG00000242103.1","gene_symbol":"AC079841.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121356991,"end":121357940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244142.1","gene_symbol":"ATP6V0CP2","gene_name":"ATPase H+ transporting V0 subunit c pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:40000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478961","summary":null,"start":111478737,"end":111478943,"strand":1,"description":"ATPase H+ transporting V0 subunit c pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:40000]"}, {"versioned_ensembl_gene_id":"ENSG00000230691.1","gene_symbol":"MRPL35P4","gene_name":"mitochondrial ribosomal protein L35 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29707]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359745","summary":null,"start":12844865,"end":12845430,"strand":-1,"description":"mitochondrial ribosomal protein L35 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29707]"}, {"versioned_ensembl_gene_id":"ENSG00000259823.5","gene_symbol":"LYPD8","gene_name":"LY6/PLAUR domain containing 8 [Source:HGNC Symbol;Acc:HGNC:44208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646627","summary":null,"start":248718649,"end":248755739,"strand":-1,"description":"LY6/PLAUR domain containing 8 [Source:HGNC Symbol;Acc:HGNC:44208]"}, {"versioned_ensembl_gene_id":"ENSG00000105219.8","gene_symbol":"CNTD2","gene_name":"cyclin N-terminal domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25805]","synonyms":"FLJ13265,CCNP","biotype":"protein_coding","ncbi_id":"79935","summary":null,"start":40222208,"end":40226690,"strand":-1,"description":"cyclin N-terminal domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25805]"}, {"versioned_ensembl_gene_id":"ENSG00000272971.1","gene_symbol":"AL365181.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156614742,"end":156615288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270526.1","gene_symbol":"SNRPGP19","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481686","summary":null,"start":65514403,"end":65514923,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49375]"}, {"versioned_ensembl_gene_id":"ENSG00000108773.10","gene_symbol":"KAT2A","gene_name":"lysine acetyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:4201]","synonyms":"GCN5,PCAF-b,GCN5L2","biotype":"protein_coding","ncbi_id":"2648","summary":"KAT2A, or GCN5, is a histone acetyltransferase (HAT) that functions primarily as a transcriptional activator. It also functions as a repressor of NF-kappa-B (see MIM 164011) by promoting ubiquitination of the NF-kappa-B subunit RELA (MIM 164014) in a HAT-independent manner (Mao et al., 2009 [PubMed 19339690]).[supplied by OMIM, Sep 2009]","start":42113108,"end":42121358,"strand":-1,"description":"lysine acetyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:4201]"}, {"versioned_ensembl_gene_id":"ENSG00000161091.12","gene_symbol":"MFSD12","gene_name":"major facilitator superfamily domain containing 12 [Source:HGNC Symbol;Acc:HGNC:28299]","synonyms":"PP3501,MGC20700,C19orf28","biotype":"protein_coding","ncbi_id":"126321","summary":null,"start":3538261,"end":3574290,"strand":-1,"description":"major facilitator superfamily domain containing 12 [Source:HGNC Symbol;Acc:HGNC:28299]"}, {"versioned_ensembl_gene_id":"ENSG00000237330.2","gene_symbol":"RNF223","gene_name":"ring finger protein 223 [Source:HGNC Symbol;Acc:HGNC:40020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401934","summary":null,"start":1070966,"end":1074307,"strand":-1,"description":"ring finger protein 223 [Source:HGNC Symbol;Acc:HGNC:40020]"}, {"versioned_ensembl_gene_id":"ENSG00000162981.13","gene_symbol":"FAM84A","gene_name":"family with sequence similarity 84 member A [Source:HGNC Symbol;Acc:HGNC:20743]","synonyms":"NSE1,FLJ35392","biotype":"protein_coding","ncbi_id":"151354","summary":null,"start":14632686,"end":14650814,"strand":1,"description":"family with sequence similarity 84 member A [Source:HGNC Symbol;Acc:HGNC:20743]"}, {"versioned_ensembl_gene_id":"ENSG00000224034.1","gene_symbol":"LINC02561","gene_name":"long intergenic non-protein coding RNA 2561 [Source:HGNC Symbol;Acc:HGNC:53601]","synonyms":"RP11-445P17.8","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5266033,"end":5271236,"strand":-1,"description":"long intergenic non-protein coding RNA 2561 [Source:HGNC Symbol;Acc:HGNC:53601]"}, {"versioned_ensembl_gene_id":"ENSG00000165972.12","gene_symbol":"CCDC38","gene_name":"coiled-coil domain containing 38 [Source:HGNC Symbol;Acc:HGNC:26843]","synonyms":"FLJ40089","biotype":"protein_coding","ncbi_id":"120935","summary":null,"start":95867048,"end":95942974,"strand":-1,"description":"coiled-coil domain containing 38 [Source:HGNC Symbol;Acc:HGNC:26843]"}, {"versioned_ensembl_gene_id":"ENSG00000140859.15","gene_symbol":"KIFC3","gene_name":"kinesin family member C3 [Source:HGNC Symbol;Acc:HGNC:6326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3801","summary":"This gene encodes a member of the kinesin-14 family of microtubule motors. Members of this family play a role in the formation, maintenance and remodeling of the bipolar mitotic spindle. The protein encoded by this gene has cytoplasmic functions in the interphase cells. It may also be involved in the final stages of cytokinesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":57758217,"end":57863053,"strand":-1,"description":"kinesin family member C3 [Source:HGNC Symbol;Acc:HGNC:6326]"}, {"versioned_ensembl_gene_id":"ENSG00000130803.14","gene_symbol":"ZNF317","gene_name":"zinc finger protein 317 [Source:HGNC Symbol;Acc:HGNC:13507]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57693","summary":null,"start":9140380,"end":9163424,"strand":1,"description":"zinc finger protein 317 [Source:HGNC Symbol;Acc:HGNC:13507]"}, {"versioned_ensembl_gene_id":"ENSG00000259884.1","gene_symbol":"AC025259.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52058459,"end":52059503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189181.4","gene_symbol":"OR14I1","gene_name":"olfactory receptor family 14 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:19575]","synonyms":"OR5BU1P,OR5BU1","biotype":"protein_coding","ncbi_id":"401994","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248681369,"end":248682304,"strand":-1,"description":"olfactory receptor family 14 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:19575]"}, {"versioned_ensembl_gene_id":"ENSG00000263241.1","gene_symbol":"MTCYBP33","gene_name":"mitochondrially encoded cytochrome b pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52301]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729143","summary":null,"start":10718633,"end":10719762,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52301]"}, {"versioned_ensembl_gene_id":"ENSG00000213962.2","gene_symbol":"API5P2","gene_name":"apoptosis inhibitor 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728664","summary":null,"start":177997273,"end":177998770,"strand":-1,"description":"apoptosis inhibitor 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39070]"}, {"versioned_ensembl_gene_id":"ENSG00000254555.1","gene_symbol":"AP003730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97908253,"end":97908537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103310.10","gene_symbol":"ZP2","gene_name":"zona pellucida glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:13188]","synonyms":"ZPA","biotype":"protein_coding","ncbi_id":"7783","summary":"The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed of three glycoproteins with various functions during fertilization and preimplantation development. The glycosylated mature peptide is one of the structural components of the zona pellucida and functions in secondary binding and penetration of acrosome-reacted spermatozoa. Female mice lacking this gene do not form a stable zona matrix and are sterile. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":21197450,"end":21214510,"strand":-1,"description":"zona pellucida glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:13188]"}, {"versioned_ensembl_gene_id":"ENSG00000248684.1","gene_symbol":"BIN2P2","gene_name":"bridging integrator 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43661]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644601","summary":null,"start":75910565,"end":75911867,"strand":1,"description":"bridging integrator 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43661]"}, {"versioned_ensembl_gene_id":"ENSG00000232647.1","gene_symbol":"POLR3KP1","gene_name":"RNA polymerase III subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39577]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289667","summary":null,"start":59071462,"end":59071803,"strand":-1,"description":"RNA polymerase III subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39577]"}, {"versioned_ensembl_gene_id":"ENSG00000243193.4","gene_symbol":"AC006387.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":107066591,"end":107133733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233710.1","gene_symbol":"AL049564.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67533163,"end":67533987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224521.1","gene_symbol":"AC098483.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":248548756,"end":248563839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189299.6","gene_symbol":"FOXR2","gene_name":"forkhead box R2 [Source:HGNC Symbol;Acc:HGNC:30469]","synonyms":"MGC21658,FOXN6","biotype":"protein_coding","ncbi_id":"139628","summary":null,"start":55623400,"end":55625325,"strand":1,"description":"forkhead box R2 [Source:HGNC Symbol;Acc:HGNC:30469]"}, {"versioned_ensembl_gene_id":"ENSG00000227298.1","gene_symbol":"ARAFP3","gene_name":"ARAF pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35474]","synonyms":"ARAF3P","biotype":"processed_pseudogene","ncbi_id":"285893","summary":null,"start":63342711,"end":63343200,"strand":1,"description":"ARAF pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35474]"}, {"versioned_ensembl_gene_id":"ENSG00000176290.8","gene_symbol":"OR4K3","gene_name":"olfactory receptor family 4 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14731]","synonyms":"OR4K3P","biotype":"polymorphic_pseudogene","ncbi_id":"283617","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":19868197,"end":19869143,"strand":-1,"description":"olfactory receptor family 4 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14731]"}, {"versioned_ensembl_gene_id":"ENSG00000226587.1","gene_symbol":"AC006455.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63326674,"end":63354326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257743.8","gene_symbol":"MGAM2","gene_name":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93432","summary":null,"start":142111749,"end":142222324,"strand":1,"description":"maltase-glucoamylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:28101]"}, {"versioned_ensembl_gene_id":"ENSG00000228304.1","gene_symbol":"OR4K6P","gene_name":"olfactory receptor family 4 subfamily K member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14748]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79314","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19847367,"end":19848263,"strand":1,"description":"olfactory receptor family 4 subfamily K member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:14748]"}, {"versioned_ensembl_gene_id":"ENSG00000233029.3","gene_symbol":"AC244453.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121090289,"end":121097655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276684.4","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55047223,"end":55079406,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000130749.9","gene_symbol":"ZC3H4","gene_name":"zinc finger CCCH-type containing 4 [Source:HGNC Symbol;Acc:HGNC:17808]","synonyms":"KIAA1064,C19orf7","biotype":"protein_coding","ncbi_id":"23211","summary":"This gene encodes a member of a family of CCCH (C-x8-C-x5-C-x3-H type) zinc finger domain-containing proteins. These zinc finger domains, which coordinate zinc finger binding and are characterized by three cysteine residues and one histidine residue, are nucleic acid-binding. Other family members are known to function in post-transcriptional regulation. [provided by RefSeq, Aug 2011]","start":47064187,"end":47113752,"strand":-1,"description":"zinc finger CCCH-type containing 4 [Source:HGNC Symbol;Acc:HGNC:17808]"}, {"versioned_ensembl_gene_id":"ENSG00000279267.1","gene_symbol":"AL078621.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":113605867,"end":113607908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237752.2","gene_symbol":"AL354685.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97906644,"end":97908090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186777.11","gene_symbol":"ZNF732","gene_name":"zinc finger protein 732 [Source:HGNC Symbol;Acc:HGNC:37138]","synonyms":"FLJ59067","biotype":"protein_coding","ncbi_id":"654254","summary":"This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and sixteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017]","start":270675,"end":305321,"strand":-1,"description":"zinc finger protein 732 [Source:HGNC Symbol;Acc:HGNC:37138]"}, {"versioned_ensembl_gene_id":"ENSG00000254183.1","gene_symbol":"AC104417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141968091,"end":141968841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227462.1","gene_symbol":"PSME2P6","gene_name":"proteasome activator subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30159]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338098","summary":null,"start":22225698,"end":22226024,"strand":1,"description":"proteasome activator subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30159]"}, {"versioned_ensembl_gene_id":"ENSG00000115221.10","gene_symbol":"ITGB6","gene_name":"integrin subunit beta 6 [Source:HGNC Symbol;Acc:HGNC:6161]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3694","summary":"This gene encodes a protein that is a member of the integrin superfamily. Members of this family are adhesion receptors that function in signaling from the extracellular matrix to the cell. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. The encoded protein forms a dimer with an alpha v chain and this heterodimer can bind to ligands like fibronectin and transforming growth factor beta 1. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":160099666,"end":160271888,"strand":-1,"description":"integrin subunit beta 6 [Source:HGNC Symbol;Acc:HGNC:6161]"}, {"versioned_ensembl_gene_id":"ENSG00000226820.2","gene_symbol":"AL592049.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66437345,"end":66440668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258564.2","gene_symbol":"OR4N1P","gene_name":"olfactory receptor family 4 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14740]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79322","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19796345,"end":19797293,"strand":1,"description":"olfactory receptor family 4 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14740]"}, {"versioned_ensembl_gene_id":"ENSG00000267120.3","gene_symbol":"AD000671.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35739252,"end":35745432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167535.7","gene_symbol":"CACNB3","gene_name":"calcium voltage-gated channel auxiliary subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:1403]","synonyms":"CACNLB3","biotype":"protein_coding","ncbi_id":"784","summary":"This gene encodes a regulatory beta subunit of the voltage-dependent calcium channel. Beta subunits are composed of five domains, which contribute to the regulation of surface expression and gating of calcium channels and may also play a role in the regulation of transcription factors and calcium transport. [provided by RefSeq, Oct 2011]","start":48813794,"end":48828941,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:1403]"}, {"versioned_ensembl_gene_id":"ENSG00000239203.1","gene_symbol":"AC093484.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16427474,"end":16428719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155903.11","gene_symbol":"RASA2","gene_name":"RAS p21 protein activator 2 [Source:HGNC Symbol;Acc:HGNC:9872]","synonyms":"GAP1M","biotype":"protein_coding","ncbi_id":"5922","summary":"The protein encoded by this gene is member of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":141487047,"end":141615342,"strand":1,"description":"RAS p21 protein activator 2 [Source:HGNC Symbol;Acc:HGNC:9872]"}, {"versioned_ensembl_gene_id":"ENSG00000126246.9","gene_symbol":"IGFLR1","gene_name":"IGF like family receptor 1 [Source:HGNC Symbol;Acc:HGNC:23620]","synonyms":"TMEM149,FLJ22573,U2AF1L4","biotype":"protein_coding","ncbi_id":"79713","summary":null,"start":35738801,"end":35742453,"strand":-1,"description":"IGF like family receptor 1 [Source:HGNC Symbol;Acc:HGNC:23620]"}, {"versioned_ensembl_gene_id":"ENSG00000224041.3","gene_symbol":"IGKV3D-15","gene_name":"immunoglobulin kappa variable 3D-15 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5824]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28875","summary":null,"start":90114838,"end":90115402,"strand":1,"description":"immunoglobulin kappa variable 3D-15 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5824]"}, {"versioned_ensembl_gene_id":"ENSG00000267781.1","gene_symbol":"SLC25A36P1","gene_name":"SLC25A36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480240","summary":null,"start":56386226,"end":56386690,"strand":1,"description":"SLC25A36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48935]"}, {"versioned_ensembl_gene_id":"ENSG00000267606.1","gene_symbol":"AC006116.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56354493,"end":56368053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225523.2","gene_symbol":"IGKV6D-21","gene_name":"immunoglobulin kappa variable 6D-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5837]","synonyms":"IGKV6D21,A10","biotype":"IG_V_gene","ncbi_id":"28870","summary":null,"start":90021567,"end":90022185,"strand":1,"description":"immunoglobulin kappa variable 6D-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5837]"}, {"versioned_ensembl_gene_id":"ENSG00000226807.6","gene_symbol":"MROH5","gene_name":"maestro heat like repeat family member 5 [Source:HGNC Symbol;Acc:HGNC:42976]","synonyms":"FLJ43860","biotype":"polymorphic_pseudogene","ncbi_id":"389690","summary":null,"start":141433829,"end":141507230,"strand":-1,"description":"maestro heat like repeat family member 5 [Source:HGNC Symbol;Acc:HGNC:42976]"}, {"versioned_ensembl_gene_id":"ENSG00000198730.7","gene_symbol":"CTR9","gene_name":"CTR9 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:16850]","synonyms":"TSBP,SH2BP1,p150TSP,KIAA0155","biotype":"protein_coding","ncbi_id":"9646","summary":"The protein encoded by this gene is a component of the PAF1 complex, which associates with RNA polymerase II and functions in transcriptional regulation and elongation. This complex also plays a role in the modification of histones. [provided by RefSeq, Oct 2016]","start":10750987,"end":10779743,"strand":1,"description":"CTR9 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:16850]"}, {"versioned_ensembl_gene_id":"ENSG00000164385.8","gene_symbol":"LINC01600","gene_name":"long intergenic non-protein coding RNA 1600 [Source:HGNC Symbol;Acc:HGNC:21600]","synonyms":"FLJ31934,C6orf195,bA145H9.2","biotype":"lincRNA","ncbi_id":"154386","summary":null,"start":2621913,"end":2634603,"strand":-1,"description":"long intergenic non-protein coding RNA 1600 [Source:HGNC Symbol;Acc:HGNC:21600]"}, {"versioned_ensembl_gene_id":"ENSG00000135365.15","gene_symbol":"PHF21A","gene_name":"PHD finger protein 21A [Source:HGNC Symbol;Acc:HGNC:24156]","synonyms":"KIAA1696,BM-006,BHC80","biotype":"protein_coding","ncbi_id":"51317","summary":"The PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron-specific genes through the cis-regulatory element known as repressor element-1 (RE1) or neural restrictive silencer (NRS) (Hakimi et al., 2002 [PubMed 12032298]).[supplied by OMIM, Nov 2010]","start":45929323,"end":46121178,"strand":-1,"description":"PHD finger protein 21A [Source:HGNC Symbol;Acc:HGNC:24156]"}, {"versioned_ensembl_gene_id":"ENSG00000216754.2","gene_symbol":"AL050335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15102946,"end":15104130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125245.12","gene_symbol":"GPR18","gene_name":"G protein-coupled receptor 18 [Source:HGNC Symbol;Acc:HGNC:4472]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2841","summary":null,"start":99254714,"end":99261744,"strand":-1,"description":"G protein-coupled receptor 18 [Source:HGNC Symbol;Acc:HGNC:4472]"}, {"versioned_ensembl_gene_id":"ENSG00000254345.1","gene_symbol":"IGKV2D-23","gene_name":"immunoglobulin kappa variable 2D-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5796]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28886","summary":null,"start":90009402,"end":90009927,"strand":1,"description":"immunoglobulin kappa variable 2D-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5796]"}, {"versioned_ensembl_gene_id":"ENSG00000249934.2","gene_symbol":"NCOA4P2","gene_name":"nuclear receptor coactivator 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52403]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728333","summary":null,"start":88508591,"end":88510403,"strand":-1,"description":"nuclear receptor coactivator 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52403]"}, {"versioned_ensembl_gene_id":"ENSG00000260514.1","gene_symbol":"AC009086.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29624517,"end":29624825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164746.13","gene_symbol":"C7orf57","gene_name":"chromosome 7 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:22247]","synonyms":null,"biotype":"protein_coding","ncbi_id":"136288","summary":null,"start":48035511,"end":48061304,"strand":1,"description":"chromosome 7 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:22247]"}, {"versioned_ensembl_gene_id":"ENSG00000196233.13","gene_symbol":"LCOR","gene_name":"ligand dependent nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:29503]","synonyms":"MLR2,KIAA1795,FLJ38026,FLJ13022,DKFZP564P1916,C10orf12","biotype":"protein_coding","ncbi_id":"84458","summary":"LCOR is a transcriptional corepressor widely expressed in fetal and adult tissues that is recruited to agonist-bound nuclear receptors through a single LxxLL motif, also referred to as a nuclear receptor (NR) box (Fernandes et al., 2003 [PubMed 12535528]).[supplied by OMIM, Mar 2008]","start":96832282,"end":96995959,"strand":1,"description":"ligand dependent nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:29503]"}, {"versioned_ensembl_gene_id":"ENSG00000260431.2","gene_symbol":"AC074051.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5207088,"end":5207439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258080.1","gene_symbol":"ARHGAP42P4","gene_name":"Rho GTPase activating protein 42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43941]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"254398","summary":null,"start":19688261,"end":19691194,"strand":1,"description":"Rho GTPase activating protein 42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43941]"}, {"versioned_ensembl_gene_id":"ENSG00000275442.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000266586.1","gene_symbol":"AC091027.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78908629,"end":78918993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224830.2","gene_symbol":"OR2X1P","gene_name":"olfactory receptor family 2 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31258]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403245","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247938973,"end":247939659,"strand":1,"description":"olfactory receptor family 2 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31258]"}, {"versioned_ensembl_gene_id":"ENSG00000250312.6","gene_symbol":"ZNF718","gene_name":"zinc finger protein 718 [Source:HGNC Symbol;Acc:HGNC:26889]","synonyms":"FLJ90036","biotype":"protein_coding","ncbi_id":"255403","summary":null,"start":124480,"end":163989,"strand":1,"description":"zinc finger protein 718 [Source:HGNC Symbol;Acc:HGNC:26889]"}, {"versioned_ensembl_gene_id":"ENSG00000177275.4","gene_symbol":"OR2AJ1","gene_name":"olfactory receptor family 2 subfamily AJ member 1 [Source:HGNC Symbol;Acc:HGNC:15001]","synonyms":"OR2AJ1P,OR2AJ1Q","biotype":"protein_coding","ncbi_id":"127608","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247924889,"end":247935339,"strand":1,"description":"olfactory receptor family 2 subfamily AJ member 1 [Source:HGNC Symbol;Acc:HGNC:15001]"}, {"versioned_ensembl_gene_id":"ENSG00000161638.10","gene_symbol":"ITGA5","gene_name":"integrin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6141]","synonyms":"FNRA,CD49e","biotype":"protein_coding","ncbi_id":"3678","summary":"The product of this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha subunit and a beta subunit that function in cell surface adhesion and signaling. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha 5 subunit. This subunit associates with the beta 1 subunit to form a fibronectin receptor. This integrin may promote tumor invasion, and higher expression of this gene may be correlated with shorter survival time in lung cancer patients. Note that the integrin alpha 5 and integrin alpha V subunits are encoded by distinct genes. [provided by RefSeq, Oct 2015]","start":54395261,"end":54419460,"strand":-1,"description":"integrin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6141]"}, {"versioned_ensembl_gene_id":"ENSG00000139572.3","gene_symbol":"GPR84","gene_name":"G protein-coupled receptor 84 [Source:HGNC Symbol;Acc:HGNC:4535]","synonyms":"EX33","biotype":"protein_coding","ncbi_id":"53831","summary":null,"start":54362445,"end":54364487,"strand":-1,"description":"G protein-coupled receptor 84 [Source:HGNC Symbol;Acc:HGNC:4535]"}, {"versioned_ensembl_gene_id":"ENSG00000198900.5","gene_symbol":"TOP1","gene_name":"topoisomerase (DNA) I [Source:HGNC Symbol;Acc:HGNC:11986]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7150","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus altering the topology of DNA. This gene is localized to chromosome 20 and has pseudogenes which reside on chromosomes 1 and 22. [provided by RefSeq, Jul 2008]","start":41028818,"end":41124487,"strand":1,"description":"topoisomerase (DNA) I [Source:HGNC Symbol;Acc:HGNC:11986]"}, {"versioned_ensembl_gene_id":"ENSG00000101310.14","gene_symbol":"SEC23B","gene_name":"Sec23 homolog B, coat complex II component [Source:HGNC Symbol;Acc:HGNC:10702]","synonyms":"HEMPAS,CDAN2,CDAII,CDA-II","biotype":"protein_coding","ncbi_id":"10483","summary":"The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The function of this gene product has been implicated in cargo selection and concentration. Multiple alternatively spliced transcript variants have been identified in this gene. [provided by RefSeq, Feb 2010]","start":18507493,"end":18561415,"strand":1,"description":"Sec23 homolog B, coat complex II component [Source:HGNC Symbol;Acc:HGNC:10702]"}, {"versioned_ensembl_gene_id":"ENSG00000226378.8","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29723672,"end":29746121,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000224564.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29788811,"end":29789808,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000270954.1","gene_symbol":"RPSAP75","gene_name":"ribosomal protein SA pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:51929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075114","summary":null,"start":74804473,"end":74804773,"strand":1,"description":"ribosomal protein SA pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:51929]"}, {"versioned_ensembl_gene_id":"ENSG00000238243.3","gene_symbol":"OR2W3","gene_name":"olfactory receptor family 2 subfamily W member 3 [Source:HGNC Symbol;Acc:HGNC:15021]","synonyms":"OST718,OR2W8P,OR2W3P","biotype":"protein_coding","ncbi_id":"343171","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247895587,"end":247896531,"strand":1,"description":"olfactory receptor family 2 subfamily W member 3 [Source:HGNC Symbol;Acc:HGNC:15021]"}, {"versioned_ensembl_gene_id":"ENSG00000101435.4","gene_symbol":"CST9L","gene_name":"cystatin 9 like [Source:HGNC Symbol;Acc:HGNC:16233]","synonyms":"CTES7B,bA218C14.1","biotype":"protein_coding","ncbi_id":"128821","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a protein similar to mouse cystatin 9. Based on its testis-specific expression, it is likely to have a role in tissue reorganization during early testis development. [provided by RefSeq, Jul 2008]","start":23564732,"end":23568749,"strand":-1,"description":"cystatin 9 like [Source:HGNC Symbol;Acc:HGNC:16233]"}, {"versioned_ensembl_gene_id":"ENSG00000205534.6","gene_symbol":"SMG1P2","gene_name":"SMG1P2, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49859]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440354","summary":null,"start":29527568,"end":29594966,"strand":-1,"description":"SMG1P2, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49859]"}, {"versioned_ensembl_gene_id":"ENSG00000172840.6","gene_symbol":"PDP2","gene_name":"pyruvate dehyrogenase phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:30263]","synonyms":"PPM2C2,PPM2B,KIAA1348","biotype":"protein_coding","ncbi_id":"57546","summary":"This gene is a mitochondrial protein that functions as a phosphatase and is involved in the enzymatic resetting of the pyruvate dehydrogenase complex. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2016]","start":66878589,"end":66895754,"strand":1,"description":"pyruvate dehyrogenase phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:30263]"}, {"versioned_ensembl_gene_id":"ENSG00000231837.2","gene_symbol":"RPS7P2","gene_name":"ribosomal protein S7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36079]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270868","summary":null,"start":154078866,"end":154079963,"strand":1,"description":"ribosomal protein S7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36079]"}, {"versioned_ensembl_gene_id":"ENSG00000276638.1","gene_symbol":"AL109954.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23489416,"end":23489973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277303.2","gene_symbol":"EPOP","gene_name":"elongin BC and polycomb repressive complex 2 associated protein [Source:HGNC Symbol;Acc:HGNC:34493]","synonyms":"PRR28,LOC100170841,C17orf96","biotype":"protein_coding","ncbi_id":"100170841","summary":null,"start":38472490,"end":38476208,"strand":-1,"description":"elongin BC and polycomb repressive complex 2 associated protein [Source:HGNC Symbol;Acc:HGNC:34493]"}, {"versioned_ensembl_gene_id":"ENSG00000283232.1","gene_symbol":"AL138921.3","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":100105754,"end":100140151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261346.1","gene_symbol":"AC116348.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30477180,"end":30489353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170485.16","gene_symbol":"NPAS2","gene_name":"neuronal PAS domain protein 2 [Source:HGNC Symbol;Acc:HGNC:7895]","synonyms":"PASD4,MOP4,bHLHe9","biotype":"protein_coding","ncbi_id":"4862","summary":"The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. A similar mouse protein may play a regulatory role in the acquisition of specific types of memory. It also may function as a part of a molecular clock operative in the mammalian forebrain. [provided by RefSeq, Jul 2008]","start":100820152,"end":100996829,"strand":1,"description":"neuronal PAS domain protein 2 [Source:HGNC Symbol;Acc:HGNC:7895]"}, {"versioned_ensembl_gene_id":"ENSG00000236027.2","gene_symbol":"PATE3","gene_name":"prostate and testis expressed 3 [Source:HGNC Symbol;Acc:HGNC:35426]","synonyms":"PATE-DJ,HEL-127","biotype":"protein_coding","ncbi_id":"100169851","summary":null,"start":125788111,"end":125791600,"strand":1,"description":"prostate and testis expressed 3 [Source:HGNC Symbol;Acc:HGNC:35426]"}, {"versioned_ensembl_gene_id":"ENSG00000265400.1","gene_symbol":"AC005244.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12201600,"end":12215267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164744.12","gene_symbol":"SUN3","gene_name":"Sad1 and UNC84 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22429]","synonyms":"SUNC1,MGC33329","biotype":"protein_coding","ncbi_id":"256979","summary":null,"start":47987148,"end":48029119,"strand":-1,"description":"Sad1 and UNC84 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22429]"}, {"versioned_ensembl_gene_id":"ENSG00000162627.16","gene_symbol":"SNX7","gene_name":"sorting nexin 7 [Source:HGNC Symbol;Acc:HGNC:14971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51375","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like some family members, and its exact function is unknown. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Jun 2010]","start":98661701,"end":98760500,"strand":1,"description":"sorting nexin 7 [Source:HGNC Symbol;Acc:HGNC:14971]"}, {"versioned_ensembl_gene_id":"ENSG00000151693.10","gene_symbol":"ASAP2","gene_name":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:2721]","synonyms":"SHAG1,PAP,KIAA0400,DDEF2,CENTB3","biotype":"protein_coding","ncbi_id":"8853","summary":"This gene encodes a multidomain protein containing an N-terminal alpha-helical region with a coiled-coil motif, followed by a pleckstrin homology (PH) domain, an Arf-GAP domain, an ankyrin homology region, a proline-rich region, and a C-terminal Src homology 3 (SH3) domain. The protein localizes in the Golgi apparatus and at the plasma membrane, where it colocalizes with protein tyrosine kinase 2-beta (PYK2). The encoded protein forms a stable complex with PYK2 in vivo. This interaction appears to be mediated by binding of its SH3 domain to the C-terminal proline-rich domain of PYK2. The encoded protein is tyrosine phosphorylated by activated PYK2. It has catalytic activity for class I and II ArfGAPs in vitro, and can bind the class III Arf ARF6 without immediate GAP activity. The encoded protein is believed to function as an ARF GAP that controls ARF-mediated vesicle budding when recruited to Golgi membranes. In addition, it functions as a substrate and downstream target for PYK2 and SRC, a pathway that may be involved in the regulation of vesicular transport. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":9206765,"end":9405683,"strand":1,"description":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:2721]"}, {"versioned_ensembl_gene_id":"ENSG00000278606.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803296,"end":54814484,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000233565.1","gene_symbol":"AC007690.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":186922286,"end":186922753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111642.14","gene_symbol":"CHD4","gene_name":"chromodomain helicase DNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:1919]","synonyms":"Mi2-BETA,Mi-2b","biotype":"protein_coding","ncbi_id":"1108","summary":"The product of this gene belongs to the SNF2/RAD54 helicase family. It represents the main component of the nucleosome remodeling and deacetylase complex and plays an important role in epigenetic transcriptional repression. Patients with dermatomyositis develop antibodies against this protein. Somatic mutations in this gene are associated with serous endometrial tumors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":6570083,"end":6607476,"strand":-1,"description":"chromodomain helicase DNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:1919]"}, {"versioned_ensembl_gene_id":"ENSG00000282763.1","gene_symbol":"AC243829.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36116177,"end":36177516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247853.2","gene_symbol":"AC006064.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6578622,"end":6584739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238133.6","gene_symbol":"MAP3K20-AS1","gene_name":"MAP3K20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27935]","synonyms":"MLK7-AS1","biotype":"antisense_RNA","ncbi_id":"339751","summary":null,"start":173166446,"end":173282036,"strand":-1,"description":"MAP3K20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27935]"}, {"versioned_ensembl_gene_id":"ENSG00000281213.1","gene_symbol":"LINC01238","gene_name":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]","synonyms":"FLJ40615,FLJ40615","biotype":"lincRNA","ncbi_id":"102723927","summary":null,"start":241970683,"end":241977276,"strand":1,"description":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]"}, {"versioned_ensembl_gene_id":"ENSG00000090487.10","gene_symbol":"SPG21","gene_name":"SPG21, maspardin [Source:HGNC Symbol;Acc:HGNC:20373]","synonyms":"MAST,GL010,BM-019,ACP33","biotype":"protein_coding","ncbi_id":"51324","summary":"The protein encoded by this gene binds to the hydrophobic C-terminal amino acids of CD4 which are involved in repression of T cell activation. The interaction with CD4 is mediated by the noncatalytic alpha/beta hydrolase fold domain of this protein. It is thus proposed that this gene product modulates the stimulatory activity of CD4. Mutations in this gene are associated with autosomal recessive spastic paraplegia 21 (SPG21), also known as mast syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":64963021,"end":64990310,"strand":-1,"description":"SPG21, maspardin [Source:HGNC Symbol;Acc:HGNC:20373]"}, {"versioned_ensembl_gene_id":"ENSG00000187537.13","gene_symbol":"POTEG","gene_name":"POTE ankyrin domain family member G [Source:HGNC Symbol;Acc:HGNC:33896]","synonyms":"POTE14alpha,POTE14,POTE-14,CT104.4,A26C2","biotype":"protein_coding","ncbi_id":"404785","summary":null,"start":19402486,"end":19434341,"strand":-1,"description":"POTE ankyrin domain family member G [Source:HGNC Symbol;Acc:HGNC:33896]"}, {"versioned_ensembl_gene_id":"ENSG00000223638.3","gene_symbol":"RFPL4A","gene_name":"ret finger protein like 4A [Source:HGNC Symbol;Acc:HGNC:16449]","synonyms":"RNF210,RFPL4","biotype":"protein_coding","ncbi_id":"342931","summary":null,"start":55759014,"end":55763175,"strand":1,"description":"ret finger protein like 4A [Source:HGNC Symbol;Acc:HGNC:16449]"}, {"versioned_ensembl_gene_id":"ENSG00000273608.4","gene_symbol":"SRCIN1","gene_name":"SRC kinase signaling inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:29506]","synonyms":"SNIP,p140Cap,KIAA1684","biotype":"protein_coding","ncbi_id":"80725","summary":null,"start":38330785,"end":38406717,"strand":-1,"description":"SRC kinase signaling inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:29506]"}, {"versioned_ensembl_gene_id":"ENSG00000159399.9","gene_symbol":"HK2","gene_name":"hexokinase 2 [Source:HGNC Symbol;Acc:HGNC:4923]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3099","summary":"Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes hexokinase 2, the predominant form found in skeletal muscle. It localizes to the outer membrane of mitochondria. Expression of this gene is insulin-responsive, and studies in rat suggest that it is involved in the increased rate of glycolysis seen in rapidly growing cancer cells. [provided by RefSeq, Apr 2009]","start":74833981,"end":74893359,"strand":1,"description":"hexokinase 2 [Source:HGNC Symbol;Acc:HGNC:4923]"}, {"versioned_ensembl_gene_id":"ENSG00000282597.1","gene_symbol":"AC244489.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16346007,"end":16346376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171509.15","gene_symbol":"RXFP1","gene_name":"relaxin/insulin like family peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:19718]","synonyms":"RXFPR1,LGR7","biotype":"protein_coding","ncbi_id":"59350","summary":"This gene encodes a member of the leucine-rich repeat-containing subgroup of the G protein-coupled 7-transmembrane receptor superfamily. The encoded protein plays a critical role in sperm motility, pregnancy and parturition as a receptor for the protein hormone relaxin. Decreased expression of this gene may play a role in endometriosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":158315311,"end":158653372,"strand":1,"description":"relaxin/insulin like family peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:19718]"}, {"versioned_ensembl_gene_id":"ENSG00000267117.1","gene_symbol":"AC010525.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55694118,"end":55694558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188938.15","gene_symbol":"FAM120AOS","gene_name":"family with sequence similarity 120A opposite strand [Source:HGNC Symbol;Acc:HGNC:23389]","synonyms":"C9orf10OS","biotype":"protein_coding","ncbi_id":"158293","summary":"Differences in the expression level of this gene are associated with the survival rate of those with glioma. [provided by RefSeq, May 2017]","start":93446494,"end":93453592,"strand":-1,"description":"family with sequence similarity 120A opposite strand [Source:HGNC Symbol;Acc:HGNC:23389]"}, {"versioned_ensembl_gene_id":"ENSG00000160868.14","gene_symbol":"CYP3A4","gene_name":"cytochrome P450 family 3 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:2637]","synonyms":"CYP3A3","biotype":"protein_coding","ncbi_id":"1576","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by glucocorticoids and some pharmacological agents. This enzyme is involved in the metabolism of approximately half the drugs in use today, including acetaminophen, codeine, cyclosporin A, diazepam, erythromycin, and chloroquine. The enzyme also metabolizes some steroids and carcinogens. This gene is part of a cluster of cytochrome P450 genes on chromosome 7q21.1. Previously another CYP3A gene, CYP3A3, was thought to exist; however, it is now thought that this sequence represents a transcript variant of CYP3A4. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2020]","start":99756960,"end":99784265,"strand":-1,"description":"cytochrome P450 family 3 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:2637]"}, {"versioned_ensembl_gene_id":"ENSG00000145384.3","gene_symbol":"FABP2","gene_name":"fatty acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3556]","synonyms":"I-FABP","biotype":"protein_coding","ncbi_id":"2169","summary":"The protein encoded by this gene is an intracellular fatty acid-binding protein that participates in the uptake, intracellular metabolism, and transport of long-chain fatty acids. The encoded protein is also involved in the modulation of cell growth and proliferation. This protein binds saturated long-chain fatty acids with high affinity, and may act as a lipid sensor to maintain energy homeostasis. [provided by RefSeq, Aug 2017]","start":119317250,"end":119322390,"strand":-1,"description":"fatty acid binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3556]"}, {"versioned_ensembl_gene_id":"ENSG00000277163.1","gene_symbol":"KIR2DS3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]","synonyms":"nkat7","biotype":"protein_coding","ncbi_id":"3808","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54782627,"end":54797062,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]"}, {"versioned_ensembl_gene_id":"ENSG00000053372.4","gene_symbol":"MRTO4","gene_name":"MRT4 homolog, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:18477]","synonyms":"dJ657E11.4,C1orf33,MRT4","biotype":"protein_coding","ncbi_id":"51154","summary":"This gene encodes a protein sharing a low level of sequence similarity with ribosomal protein P0. While the precise function of the encoded protein is currently unknown, it appears to be involved in mRNA turnover and ribosome assembly. [provided by RefSeq, Jul 2008]","start":19251539,"end":19260128,"strand":1,"description":"MRT4 homolog, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:18477]"}, {"versioned_ensembl_gene_id":"ENSG00000171425.9","gene_symbol":"ZNF581","gene_name":"zinc finger protein 581 [Source:HGNC Symbol;Acc:HGNC:25017]","synonyms":"HSPC189,FLJ22550","biotype":"protein_coding","ncbi_id":"51545","summary":null,"start":55635459,"end":55645622,"strand":1,"description":"zinc finger protein 581 [Source:HGNC Symbol;Acc:HGNC:25017]"}, {"versioned_ensembl_gene_id":"ENSG00000249316.2","gene_symbol":"AF131216.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11281364,"end":11282501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270802.2","gene_symbol":"AC005776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15338948,"end":15339237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254297.1","gene_symbol":"AC091820.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167296234,"end":167303372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235730.1","gene_symbol":"OR2AF1P","gene_name":"olfactory receptor family 2 subfamily AF member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14719]","synonyms":"OR2AF2P","biotype":"processed_pseudogene","ncbi_id":"79331","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131619021,"end":131619909,"strand":1,"description":"olfactory receptor family 2 subfamily AF member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14719]"}, {"versioned_ensembl_gene_id":"ENSG00000281099.1","gene_symbol":"AC244167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242003691,"end":242006013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277128.1","gene_symbol":"AL589743.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19127736,"end":19175530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281806.1","gene_symbol":"AC208876.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":745961,"end":754657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241296.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":33025327,"end":33043825,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000196143.4","gene_symbol":"OR11H13P","gene_name":"olfactory receptor family 11 subfamily H member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:29997]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440159","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19180291,"end":19181269,"strand":1,"description":"olfactory receptor family 11 subfamily H member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:29997]"}, {"versioned_ensembl_gene_id":"ENSG00000075188.8","gene_symbol":"NUP37","gene_name":"nucleoporin 37 [Source:HGNC Symbol;Acc:HGNC:29929]","synonyms":"FLJ22618,MGC5585","biotype":"protein_coding","ncbi_id":"79023","summary":"Nuclear pore complexes (NPCs) are used for transporting macromolecules between the cytoplasm and the nucleus. NPCs consist of multiple copies of 30 distinct proteins (nucleoporins), which assemble into biochemically-separable subcomplexes. The protein encoded by this gene is part of a subcomplex (Nup107-160) that is required for proper NPC function as well as for normal kinetochore-microtubule interaction and mitosis. [provided by RefSeq, Dec 2015]","start":102073103,"end":102120124,"strand":-1,"description":"nucleoporin 37 [Source:HGNC Symbol;Acc:HGNC:29929]"}, {"versioned_ensembl_gene_id":"ENSG00000281358.1","gene_symbol":"RASSF1-AS1","gene_name":"RASSF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49091]","synonyms":"ANRASSF1","biotype":"antisense_RNA","ncbi_id":"102060282","summary":null,"start":50337511,"end":50338300,"strand":1,"description":"RASSF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49091]"}, {"versioned_ensembl_gene_id":"ENSG00000280538.1","gene_symbol":"AC208876.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":753629,"end":754224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271632.1","gene_symbol":"AL589743.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19199763,"end":19200279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132535.18","gene_symbol":"DLG4","gene_name":"discs large MAGUK scaffold protein 4 [Source:HGNC Symbol;Acc:HGNC:2903]","synonyms":"SAP90,SAP-90,PSD95,PSD-95","biotype":"protein_coding","ncbi_id":"1742","summary":"This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. It heteromultimerizes with another MAGUK protein, DLG2, and is recruited into NMDA receptor and potassium channel clusters. These two MAGUK proteins may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":7189890,"end":7219702,"strand":-1,"description":"discs large MAGUK scaffold protein 4 [Source:HGNC Symbol;Acc:HGNC:2903]"}, {"versioned_ensembl_gene_id":"ENSG00000205085.11","gene_symbol":"FAM71F2","gene_name":"family with sequence similarity 71 member F2 [Source:HGNC Symbol;Acc:HGNC:27998]","synonyms":"FAM137B","biotype":"protein_coding","ncbi_id":"346653","summary":null,"start":128672288,"end":128687872,"strand":1,"description":"family with sequence similarity 71 member F2 [Source:HGNC Symbol;Acc:HGNC:27998]"}, {"versioned_ensembl_gene_id":"ENSG00000277069.2","gene_symbol":"RXFP3","gene_name":"relaxin/insulin like family peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:24883]","synonyms":"SALPR,RXFPR3,RLN3R1,GPCR135","biotype":"protein_coding","ncbi_id":"51289","summary":null,"start":33938372,"end":33940223,"strand":1,"description":"relaxin/insulin like family peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:24883]"}, {"versioned_ensembl_gene_id":"ENSG00000189326.4","gene_symbol":"SPANXN4","gene_name":"SPANX family member N4 [Source:HGNC Symbol;Acc:HGNC:33177]","synonyms":"SPANX-N4,CT11.9","biotype":"protein_coding","ncbi_id":"441525","summary":"This gene represents one of several duplicated family members that are located on the X chromosome. This gene family encodes proteins that play a role in spermiogenesis. These proteins represent a specific subgroup of cancer/testis-associated antigens, and they may be candidates for tumor vaccines. This family member belongs to a subgroup of related genes that are present in all primates and rats and mice, and thus, it represents one of the ancestral family members. [provided by RefSeq, Sep 2009]","start":143025918,"end":143034702,"strand":1,"description":"SPANX family member N4 [Source:HGNC Symbol;Acc:HGNC:33177]"}, {"versioned_ensembl_gene_id":"ENSG00000185033.14","gene_symbol":"SEMA4B","gene_name":"semaphorin 4B [Source:HGNC Symbol;Acc:HGNC:10730]","synonyms":"SemC,SEMAC,MGC131831,KIAA1745","biotype":"protein_coding","ncbi_id":"10509","summary":null,"start":90160604,"end":90229679,"strand":1,"description":"semaphorin 4B [Source:HGNC Symbol;Acc:HGNC:10730]"}, {"versioned_ensembl_gene_id":"ENSG00000281362.1","gene_symbol":"LINC01115","gene_name":"long intergenic non-protein coding RNA 1115 [Source:NCBI gene;Acc:339822]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339822","summary":null,"start":784657,"end":859032,"strand":-1,"description":"long intergenic non-protein coding RNA 1115 [Source:NCBI gene;Acc:339822]"}, {"versioned_ensembl_gene_id":"ENSG00000078699.21","gene_symbol":"CBFA2T2","gene_name":"CBFA2/RUNX1 translocation partner 2 [Source:HGNC Symbol;Acc:HGNC:1536]","synonyms":"ZMYND3,MTGR1","biotype":"protein_coding","ncbi_id":"9139","summary":"In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5'-region of the RUNX1 (AML1) gene fused to the 3'-region of the CBFA2T1 (MTG8) gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. The protein encoded by this gene binds to the AML1-MTG8 complex and may be important in promoting leukemogenesis. Several transcript variants are thought to exist for this gene, but the full-length natures of only three have been described. [provided by RefSeq, Jul 2008]","start":33490075,"end":33650036,"strand":1,"description":"CBFA2/RUNX1 translocation partner 2 [Source:HGNC Symbol;Acc:HGNC:1536]"}, {"versioned_ensembl_gene_id":"ENSG00000105514.7","gene_symbol":"RAB3D","gene_name":"RAB3D, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9779]","synonyms":"RAD3D,RAB16,GOV,D2-2","biotype":"protein_coding","ncbi_id":"9545","summary":null,"start":11322046,"end":11346270,"strand":-1,"description":"RAB3D, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9779]"}, {"versioned_ensembl_gene_id":"ENSG00000242553.1","gene_symbol":"AP001432.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37221419,"end":37237744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157538.13","gene_symbol":"DSCR3","gene_name":"DSCR3 arrestin fold containing [Source:HGNC Symbol;Acc:HGNC:3044]","synonyms":"DCRA","biotype":"protein_coding","ncbi_id":"10311","summary":"The region of chromosome 21 between genes CBR and ERG (CBR-ERG region), which spans 2.5 Mb on 21q22.2, has been defined by analysis of patients with partial trisomy 21. It contributes significantly to the pathogenesis of many characteristics of Down syndrome, including morphological features, hypotonia, and cognitive disability. The DSCR3 (Down syndrome critical region gene 3) gene is found in this region and is predictated to contain eight exons. DSCR3 is expressed in most tissues examined. [provided by RefSeq, Jul 2008]","start":37223420,"end":37267919,"strand":-1,"description":"DSCR3 arrestin fold containing [Source:HGNC Symbol;Acc:HGNC:3044]"}, {"versioned_ensembl_gene_id":"ENSG00000223436.1","gene_symbol":"AC011625.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132352334,"end":132367976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281919.2","gene_symbol":"SLC45A2","gene_name":"solute carrier family 45 member 2 [Source:HGNC Symbol;Acc:HGNC:16472]","synonyms":"OCA4,MATP,AIM-1","biotype":"protein_coding","ncbi_id":"51151","summary":"This gene encodes a transporter protein that mediates melanin synthesis. The protein is expressed in a high percentage of melanoma cell lines. Mutations in this gene are a cause of oculocutaneous albinism type 4, and polymorphisms in this gene are associated with variations in skin and hair color. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":33946602,"end":33956490,"strand":-1,"description":"solute carrier family 45 member 2 [Source:HGNC Symbol;Acc:HGNC:16472]"}, {"versioned_ensembl_gene_id":"ENSG00000242534.2","gene_symbol":"IGKV2D-28","gene_name":"immunoglobulin kappa variable 2D-28 [Source:HGNC Symbol;Acc:HGNC:5799]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28883","summary":null,"start":89959979,"end":89960754,"strand":1,"description":"immunoglobulin kappa variable 2D-28 [Source:HGNC Symbol;Acc:HGNC:5799]"}, {"versioned_ensembl_gene_id":"ENSG00000225144.2","gene_symbol":"AC018643.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132264152,"end":132271269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109083.13","gene_symbol":"IFT20","gene_name":"intraflagellar transport 20 [Source:HGNC Symbol;Acc:HGNC:30989]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90410","summary":"This gene encodes a intraflagellar transport protein important for intracellular transport. The encoded protein forms part of a complex involved in trafficking of proteins from the Golgi body, including recycling of immune signalling components (Finetti et al., PubMed: 19855387). This gene is part of a complex set of sense-antisense loci that may be co-regulated. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 14.[provided by RefSeq, Jun 2012]","start":28328325,"end":28335489,"strand":-1,"description":"intraflagellar transport 20 [Source:HGNC Symbol;Acc:HGNC:30989]"}, {"versioned_ensembl_gene_id":"ENSG00000282301.1","gene_symbol":"CYP3A7-CYP3A51P","gene_name":"CYP3A7-CYP3A51P readthrough [Source:HGNC Symbol;Acc:HGNC:51504]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100861540","summary":"This locus represents readthrough transcription between the neighboring CYP3A7 (cytochrome P450, family 3, subfamily A, polypeptide 7) and CYP3A51P (cytochrome P450, family 3, subfamily A, polypeptide 51, pseudogene) genes, which are members of the CYP3A gene cluster on chromosome 7. The downstream pseudogene is not known to be independently transcribed. The readthrough transcript includes CYP3A7 exons 1-13 and exons 2 and 13 of the pseudogene. It encodes a CYP3A isoform with a novel C-terminus. This isoform is only expressed in alleles containing a T nucleotide at the -6 position of a splice acceptor in the pseudogene, which enables correct splicing of the upstream CYP3A7 exons to the pseudogene exons. It should be noted that the reference genome sequence represents the CYP3A7_39256 T->A allele, and thus this haplotype is unlikely to produce the readthrough transcript. [provided by RefSeq, Jan 2015]","start":99684957,"end":99735102,"strand":-1,"description":"CYP3A7-CYP3A51P readthrough [Source:HGNC Symbol;Acc:HGNC:51504]"}, {"versioned_ensembl_gene_id":"ENSG00000224607.4","gene_symbol":"IGKV1D-27","gene_name":"immunoglobulin kappa variable 1D-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5751]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28898","summary":null,"start":89968867,"end":89969335,"strand":1,"description":"immunoglobulin kappa variable 1D-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5751]"}, {"versioned_ensembl_gene_id":"ENSG00000265144.1","gene_symbol":"MIR548AM","gene_name":"microRNA 548am [Source:HGNC Symbol;Acc:HGNC:41637]","synonyms":"hsa-mir-548am","biotype":"miRNA","ncbi_id":"100616428","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16627012,"end":16627085,"strand":-1,"description":"microRNA 548am [Source:HGNC Symbol;Acc:HGNC:41637]"}, {"versioned_ensembl_gene_id":"ENSG00000273767.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121949412,"end":121949487,"strand":-1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000276723.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65573384,"end":65573495,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201367.1","gene_symbol":"RNU6-522P","gene_name":"RNA, U6 small nuclear 522, pseudogene [Source:HGNC Symbol;Acc:HGNC:47485]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479797","summary":null,"start":15314920,"end":15315026,"strand":1,"description":"RNA, U6 small nuclear 522, pseudogene [Source:HGNC Symbol;Acc:HGNC:47485]"}, {"versioned_ensembl_gene_id":"ENSG00000238529.1","gene_symbol":"RNU6-599P","gene_name":"RNA, U6 small nuclear 599, pseudogene [Source:HGNC Symbol;Acc:HGNC:47562]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481370","summary":null,"start":42863200,"end":42863306,"strand":1,"description":"RNA, U6 small nuclear 599, pseudogene [Source:HGNC Symbol;Acc:HGNC:47562]"}, {"versioned_ensembl_gene_id":"ENSG00000201563.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32705403,"end":32705506,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278625.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":51009,"end":51114,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000277371.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":125869295,"end":125869576,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000251868.1","gene_symbol":"RNU7-71P","gene_name":"RNA, U7 small nuclear 71 pseudogene [Source:HGNC Symbol;Acc:HGNC:34167]","synonyms":"U7.71","biotype":"snRNA","ncbi_id":"100151668","summary":null,"start":72821933,"end":72821992,"strand":-1,"description":"RNA, U7 small nuclear 71 pseudogene [Source:HGNC Symbol;Acc:HGNC:34167]"}, {"versioned_ensembl_gene_id":"ENSG00000275472.1","gene_symbol":"ZNRD1-AS1_1","gene_name":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30026277,"end":30026344,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]"}, {"versioned_ensembl_gene_id":"ENSG00000271394.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35889558,"end":35889804,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000222427.1","gene_symbol":"RNA5SP338","gene_name":"RNA, 5S ribosomal pseudogene 338 [Source:HGNC Symbol;Acc:HGNC:43238]","synonyms":"RN5S338","biotype":"rRNA","ncbi_id":"100873601","summary":null,"start":22688351,"end":22688435,"strand":1,"description":"RNA, 5S ribosomal pseudogene 338 [Source:HGNC Symbol;Acc:HGNC:43238]"}, {"versioned_ensembl_gene_id":"ENSG00000112981.4","gene_symbol":"NME5","gene_name":"NME/NM23 family member 5 [Source:HGNC Symbol;Acc:HGNC:7853]","synonyms":"RSPH23,nm23-H5","biotype":"protein_coding","ncbi_id":"8382","summary":null,"start":138115172,"end":138139443,"strand":-1,"description":"NME/NM23 family member 5 [Source:HGNC Symbol;Acc:HGNC:7853]"}, {"versioned_ensembl_gene_id":"ENSG00000277198.1","gene_symbol":"RN7SL270P","gene_name":"RNA, 7SL, cytoplasmic 270, pseudogene [Source:HGNC Symbol;Acc:HGNC:46286]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480995","summary":null,"start":47041825,"end":47042105,"strand":1,"description":"RNA, 7SL, cytoplasmic 270, pseudogene [Source:HGNC Symbol;Acc:HGNC:46286]"}, {"versioned_ensembl_gene_id":"ENSG00000276103.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":150608507,"end":150608623,"strand":-1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000206618.1","gene_symbol":"RNU6-1264P","gene_name":"RNA, U6 small nuclear 1264, pseudogene [Source:HGNC Symbol;Acc:HGNC:48227]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480117","summary":null,"start":6207163,"end":6207269,"strand":1,"description":"RNA, U6 small nuclear 1264, pseudogene [Source:HGNC Symbol;Acc:HGNC:48227]"}, {"versioned_ensembl_gene_id":"ENSG00000267828.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75297990,"end":75298091,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200917.1","gene_symbol":"RNU6-553P","gene_name":"RNA, U6 small nuclear 553, pseudogene [Source:HGNC Symbol;Acc:HGNC:47516]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480589","summary":null,"start":105406997,"end":105407092,"strand":1,"description":"RNA, U6 small nuclear 553, pseudogene [Source:HGNC Symbol;Acc:HGNC:47516]"}, {"versioned_ensembl_gene_id":"ENSG00000253039.1","gene_symbol":"RNA5SP47","gene_name":"RNA, 5S ribosomal pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:42823]","synonyms":"RN5S47","biotype":"rRNA","ncbi_id":"100873286","summary":null,"start":44932323,"end":44932431,"strand":1,"description":"RNA, 5S ribosomal pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:42823]"}, {"versioned_ensembl_gene_id":"ENSG00000273964.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28629794,"end":28629883,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274706.1","gene_symbol":"RNU6-821P","gene_name":"RNA, U6 small nuclear 821, pseudogene [Source:HGNC Symbol;Acc:HGNC:47784]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481440","summary":null,"start":198071311,"end":198071417,"strand":-1,"description":"RNA, U6 small nuclear 821, pseudogene [Source:HGNC Symbol;Acc:HGNC:47784]"}, {"versioned_ensembl_gene_id":"ENSG00000252828.1","gene_symbol":"RNA5SP135","gene_name":"RNA, 5S ribosomal pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:43035]","synonyms":"RN5S135","biotype":"rRNA","ncbi_id":"100873403","summary":null,"start":68882967,"end":68883091,"strand":1,"description":"RNA, 5S ribosomal pseudogene 135 [Source:HGNC Symbol;Acc:HGNC:43035]"}, {"versioned_ensembl_gene_id":"ENSG00000275770.1","gene_symbol":"MIR6505","gene_name":"microRNA 6505 [Source:HGNC Symbol;Acc:HGNC:50104]","synonyms":"hsa-mir-6505","biotype":"miRNA","ncbi_id":"102466657","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48132797,"end":48132867,"strand":1,"description":"microRNA 6505 [Source:HGNC Symbol;Acc:HGNC:50104]"}, {"versioned_ensembl_gene_id":"ENSG00000223024.1","gene_symbol":"RNU6-55P","gene_name":"RNA, U6 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:42545]","synonyms":"RNU6-55","biotype":"snRNA","ncbi_id":"100873763","summary":null,"start":18869185,"end":18869291,"strand":-1,"description":"RNA, U6 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:42545]"}, {"versioned_ensembl_gene_id":"ENSG00000251746.1","gene_symbol":"RNA5SP112","gene_name":"RNA, 5S ribosomal pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:42910]","synonyms":"RN5S112","biotype":"rRNA","ncbi_id":"100873382","summary":null,"start":177138699,"end":177138797,"strand":1,"description":"RNA, 5S ribosomal pseudogene 112 [Source:HGNC Symbol;Acc:HGNC:42910]"}, {"versioned_ensembl_gene_id":"ENSG00000207818.1","gene_symbol":"MIR105-2","gene_name":"microRNA 105-2 [Source:HGNC Symbol;Acc:HGNC:31493]","synonyms":"MIRN105-2,hsa-mir-105-2","biotype":"miRNA","ncbi_id":"406898","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152394412,"end":152394492,"strand":-1,"description":"microRNA 105-2 [Source:HGNC Symbol;Acc:HGNC:31493]"}, {"versioned_ensembl_gene_id":"ENSG00000277178.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000275651.1","gene_symbol":"MIR6851","gene_name":"microRNA 6851 [Source:HGNC Symbol;Acc:HGNC:50083]","synonyms":"hsa-mir-6851","biotype":"miRNA","ncbi_id":"102465512","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33467869,"end":33467935,"strand":-1,"description":"microRNA 6851 [Source:HGNC Symbol;Acc:HGNC:50083]"}, {"versioned_ensembl_gene_id":"ENSG00000276100.1","gene_symbol":"ST7-OT4_3","gene_name":"ST7 overlapping transcript 4 conserved region 3 [Source:RFAM;Acc:RF02189]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116956431,"end":116956723,"strand":1,"description":"ST7 overlapping transcript 4 conserved region 3 [Source:RFAM;Acc:RF02189]"}, {"versioned_ensembl_gene_id":"ENSG00000284280.1","gene_symbol":"MIR6843","gene_name":"microRNA 6843 [Source:HGNC Symbol;Acc:HGNC:50240]","synonyms":"hsa-mir-6843","biotype":"miRNA","ncbi_id":"102465508","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27610601,"end":27610751,"strand":-1,"description":"microRNA 6843 [Source:HGNC Symbol;Acc:HGNC:50240]"}, {"versioned_ensembl_gene_id":"ENSG00000252956.1","gene_symbol":"RNA5SP40","gene_name":"RNA, 5S ribosomal pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:42816]","synonyms":"RN5S40","biotype":"rRNA","ncbi_id":"100873279","summary":null,"start":9437669,"end":9437778,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:42816]"}, {"versioned_ensembl_gene_id":"ENSG00000284665.1","gene_symbol":"AC002472.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21071082,"end":21081018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266194.1","gene_symbol":"MIR4661","gene_name":"microRNA 4661 [Source:HGNC Symbol;Acc:HGNC:41582]","synonyms":"hsa-mir-4661","biotype":"miRNA","ncbi_id":"100616245","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91205485,"end":91205559,"strand":1,"description":"microRNA 4661 [Source:HGNC Symbol;Acc:HGNC:41582]"}, {"versioned_ensembl_gene_id":"ENSG00000200389.1","gene_symbol":"RNU6-509P","gene_name":"RNA, U6 small nuclear 509, pseudogene [Source:HGNC Symbol;Acc:HGNC:47472]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479792","summary":null,"start":141902924,"end":141903030,"strand":-1,"description":"RNA, U6 small nuclear 509, pseudogene [Source:HGNC Symbol;Acc:HGNC:47472]"}, {"versioned_ensembl_gene_id":"ENSG00000277428.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37434,"end":37534,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201047.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73082494,"end":73082595,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000253070.1","gene_symbol":"RNU6-794P","gene_name":"RNA, U6 small nuclear 794, pseudogene [Source:HGNC Symbol;Acc:HGNC:47757]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480400","summary":null,"start":35231331,"end":35231394,"strand":-1,"description":"RNA, U6 small nuclear 794, pseudogene [Source:HGNC Symbol;Acc:HGNC:47757]"}, {"versioned_ensembl_gene_id":"ENSG00000278470.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32326292,"end":32326396,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207329.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":109324685,"end":109324796,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284173.1","gene_symbol":"MIR6513","gene_name":"microRNA 6513 [Source:HGNC Symbol;Acc:HGNC:50247]","synonyms":"hsa-mir-6513","biotype":"miRNA","ncbi_id":"102465256","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":218280125,"end":218280188,"strand":-1,"description":"microRNA 6513 [Source:HGNC Symbol;Acc:HGNC:50247]"}, {"versioned_ensembl_gene_id":"ENSG00000200645.1","gene_symbol":"RNU6-1210P","gene_name":"RNA, U6 small nuclear 1210, pseudogene [Source:HGNC Symbol;Acc:HGNC:48173]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481562","summary":null,"start":14759188,"end":14759294,"strand":1,"description":"RNA, U6 small nuclear 1210, pseudogene [Source:HGNC Symbol;Acc:HGNC:48173]"}, {"versioned_ensembl_gene_id":"ENSG00000284368.1","gene_symbol":"MIR5047","gene_name":"microRNA 5047 [Source:HGNC Symbol;Acc:HGNC:41834]","synonyms":"hsa-mir-5047","biotype":"miRNA","ncbi_id":"100616408","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64501214,"end":64501313,"strand":-1,"description":"microRNA 5047 [Source:HGNC Symbol;Acc:HGNC:41834]"}, {"versioned_ensembl_gene_id":"ENSG00000251788.1","gene_symbol":"RNU5A-7P","gene_name":"RNA, U5A small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42529]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873872","summary":null,"start":64228560,"end":64228675,"strand":-1,"description":"RNA, U5A small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:42529]"}, {"versioned_ensembl_gene_id":"ENSG00000265831.1","gene_symbol":"MIR3123","gene_name":"microRNA 3123 [Source:HGNC Symbol;Acc:HGNC:38330]","synonyms":"hsa-mir-3123","biotype":"miRNA","ncbi_id":"100422856","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":241132272,"end":241132346,"strand":1,"description":"microRNA 3123 [Source:HGNC Symbol;Acc:HGNC:38330]"}, {"versioned_ensembl_gene_id":"ENSG00000284386.1","gene_symbol":"MIR147B","gene_name":"microRNA 147b [Source:HGNC Symbol;Acc:HGNC:33655]","synonyms":"MIRN147B,hsa-mir-147b","biotype":"miRNA","ncbi_id":"100126311","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45433050,"end":45433129,"strand":1,"description":"microRNA 147b [Source:HGNC Symbol;Acc:HGNC:33655]"}, {"versioned_ensembl_gene_id":"ENSG00000203411.3","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":75120265,"end":75120562,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000274176.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000207982.1","gene_symbol":"MIR548B","gene_name":"microRNA 548b [Source:HGNC Symbol;Acc:HGNC:32799]","synonyms":"MIRN548B,hsa-mir-548b","biotype":"miRNA","ncbi_id":"693128","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119069047,"end":119069143,"strand":-1,"description":"microRNA 548b [Source:HGNC Symbol;Acc:HGNC:32799]"}, {"versioned_ensembl_gene_id":"ENSG00000275036.1","gene_symbol":"MIR8086","gene_name":"microRNA 8086 [Source:HGNC Symbol;Acc:HGNC:50107]","synonyms":"hsa-mir-8086","biotype":"miRNA","ncbi_id":"102465880","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28289258,"end":28289350,"strand":-1,"description":"microRNA 8086 [Source:HGNC Symbol;Acc:HGNC:50107]"}, {"versioned_ensembl_gene_id":"ENSG00000201663.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7850717,"end":7850818,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252697.1","gene_symbol":"RN7SKP209","gene_name":"RNA, 7SK small nuclear pseudogene 209 [Source:HGNC Symbol;Acc:HGNC:45933]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479188","summary":null,"start":87083233,"end":87083536,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 209 [Source:HGNC Symbol;Acc:HGNC:45933]"}, {"versioned_ensembl_gene_id":"ENSG00000200849.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10232611,"end":10232712,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252928.1","gene_symbol":"RNU6-64P","gene_name":"RNA, U6 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:42554]","synonyms":"RNU6-64","biotype":"snRNA","ncbi_id":"100873769","summary":null,"start":30281765,"end":30281869,"strand":1,"description":"RNA, U6 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:42554]"}, {"versioned_ensembl_gene_id":"ENSG00000200738.1","gene_symbol":"RNA5SP472","gene_name":"RNA, 5S ribosomal pseudogene 472 [Source:HGNC Symbol;Acc:HGNC:43372]","synonyms":"RN5S472","biotype":"rRNA","ncbi_id":"100873715","summary":null,"start":32243965,"end":32244083,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 472 [Source:HGNC Symbol;Acc:HGNC:43372]"}, {"versioned_ensembl_gene_id":"ENSG00000207307.1","gene_symbol":"RNU6-145P","gene_name":"RNA, U6 small nuclear 145, pseudogene [Source:HGNC Symbol;Acc:HGNC:47108]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479630","summary":null,"start":76532222,"end":76532327,"strand":-1,"description":"RNA, U6 small nuclear 145, pseudogene [Source:HGNC Symbol;Acc:HGNC:47108]"}, {"versioned_ensembl_gene_id":"ENSG00000265164.1","gene_symbol":"MIR2681","gene_name":"microRNA 2681 [Source:HGNC Symbol;Acc:HGNC:41532]","synonyms":"hsa-mir-2681","biotype":"miRNA","ncbi_id":"100616110","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101967642,"end":101967746,"strand":-1,"description":"microRNA 2681 [Source:HGNC Symbol;Acc:HGNC:41532]"}, {"versioned_ensembl_gene_id":"ENSG00000275788.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30684029,"end":30684278,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000206827.1","gene_symbol":"RNU6-1032P","gene_name":"RNA, U6 small nuclear 1032, pseudogene [Source:HGNC Symbol;Acc:HGNC:47995]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481506","summary":null,"start":22647582,"end":22647688,"strand":1,"description":"RNA, U6 small nuclear 1032, pseudogene [Source:HGNC Symbol;Acc:HGNC:47995]"}, {"versioned_ensembl_gene_id":"ENSG00000243029.3","gene_symbol":"RN7SL635P","gene_name":"RNA, 7SL, cytoplasmic 635, pseudogene [Source:HGNC Symbol;Acc:HGNC:46651]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479454","summary":null,"start":65545401,"end":65545696,"strand":-1,"description":"RNA, 7SL, cytoplasmic 635, pseudogene [Source:HGNC Symbol;Acc:HGNC:46651]"}, {"versioned_ensembl_gene_id":"ENSG00000275616.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43239921,"end":43240111,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000242794.2","gene_symbol":"RN7SL299P","gene_name":"RNA, 7SL, cytoplasmic 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:46315]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479331","summary":null,"start":232222866,"end":232223145,"strand":1,"description":"RNA, 7SL, cytoplasmic 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:46315]"}, {"versioned_ensembl_gene_id":"ENSG00000252688.1","gene_symbol":"RNU6-579P","gene_name":"RNA, U6 small nuclear 579, pseudogene [Source:HGNC Symbol;Acc:HGNC:47542]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481364","summary":null,"start":133333829,"end":133333930,"strand":1,"description":"RNA, U6 small nuclear 579, pseudogene [Source:HGNC Symbol;Acc:HGNC:47542]"}, {"versioned_ensembl_gene_id":"ENSG00000264153.1","gene_symbol":"SNORA38","gene_name":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]","synonyms":"ACA38,ACA38","biotype":"snoRNA","ncbi_id":"677820","summary":null,"start":31613305,"end":31613436,"strand":1,"description":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]"}, {"versioned_ensembl_gene_id":"ENSG00000276019.1","gene_symbol":"HULC","gene_name":"Highly up-regulated in liver cancer conserved region [Source:RFAM;Acc:RF02101]","synonyms":"NCRNA00078,LINC00078,HCCAT1","biotype":"misc_RNA","ncbi_id":"728655","summary":"This gene produces a long RNA that was discovered as upregulated in hepatocellular carcinoma and is associated with cancer progression. Expression of this transcript is regulated by microRNAs and at the transcriptional level by Sp1 family factors. The transcript may regulate gene expression by functioning as a competing RNA for microRNAs. [provided by RefSeq, Dec 2017]","start":8653558,"end":8653797,"strand":1,"description":"Highly up-regulated in liver cancer conserved region [Source:RFAM;Acc:RF02101]"}, {"versioned_ensembl_gene_id":"ENSG00000239468.3","gene_symbol":"RN7SL569P","gene_name":"RNA, 7SL, cytoplasmic 569, pseudogene [Source:HGNC Symbol;Acc:HGNC:46585]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481077","summary":null,"start":148890226,"end":148890513,"strand":1,"description":"RNA, 7SL, cytoplasmic 569, pseudogene [Source:HGNC Symbol;Acc:HGNC:46585]"}, {"versioned_ensembl_gene_id":"ENSG00000200021.1","gene_symbol":"RNA5SP448","gene_name":"RNA, 5S ribosomal pseudogene 448 [Source:HGNC Symbol;Acc:HGNC:43348]","synonyms":"RN5S448","biotype":"rRNA","ncbi_id":"106479015","summary":null,"start":74417594,"end":74417704,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 448 [Source:HGNC Symbol;Acc:HGNC:43348]"}, {"versioned_ensembl_gene_id":"ENSG00000212536.1","gene_symbol":"RNA5SP474","gene_name":"RNA, 5S ribosomal pseudogene 474 [Source:HGNC Symbol;Acc:HGNC:43374]","synonyms":"RN5S474","biotype":"rRNA","ncbi_id":"100873716","summary":null,"start":5098387,"end":5098476,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 474 [Source:HGNC Symbol;Acc:HGNC:43374]"}, {"versioned_ensembl_gene_id":"ENSG00000199959.1","gene_symbol":"SNORA2","gene_name":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":84277321,"end":84277457,"strand":1,"description":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]"}, {"versioned_ensembl_gene_id":"ENSG00000283450.1","gene_symbol":"MIR486-2","gene_name":"microRNA 486-2 [Source:HGNC Symbol;Acc:HGNC:50213]","synonyms":"hsa-mir-486-2","biotype":"miRNA","ncbi_id":"102465696","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41660444,"end":41660507,"strand":1,"description":"microRNA 486-2 [Source:HGNC Symbol;Acc:HGNC:50213]"}, {"versioned_ensembl_gene_id":"ENSG00000275117.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31,PRP31","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000278449.1","gene_symbol":"MIR6892","gene_name":"microRNA 6892 [Source:HGNC Symbol;Acc:HGNC:50053]","synonyms":"hsa-mir-6892","biotype":"miRNA","ncbi_id":"102465538","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143382686,"end":143382800,"strand":1,"description":"microRNA 6892 [Source:HGNC Symbol;Acc:HGNC:50053]"}, {"versioned_ensembl_gene_id":"ENSG00000200544.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33352788,"end":33352874,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251924.1","gene_symbol":"RNA5SP408","gene_name":"RNA, 5S ribosomal pseudogene 408 [Source:HGNC Symbol;Acc:HGNC:43308]","synonyms":"RN5S408","biotype":"rRNA","ncbi_id":"100873660","summary":null,"start":35735372,"end":35735471,"strand":1,"description":"RNA, 5S ribosomal pseudogene 408 [Source:HGNC Symbol;Acc:HGNC:43308]"}, {"versioned_ensembl_gene_id":"ENSG00000252526.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":50151642,"end":50151731,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000277344.1","gene_symbol":"RNU1-6P","gene_name":"RNA, U1 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:48305]","synonyms":"RNU1-6","biotype":"snRNA","ncbi_id":"106480152","summary":null,"start":16534081,"end":16534224,"strand":-1,"description":"RNA, U1 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:48305]"}, {"versioned_ensembl_gene_id":"ENSG00000264293.2","gene_symbol":"RN7SL657P","gene_name":"RNA, 7SL, cytoplasmic 657, pseudogene [Source:HGNC Symbol;Acc:HGNC:46673]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107074708","summary":null,"start":1405460,"end":1405752,"strand":-1,"description":"RNA, 7SL, cytoplasmic 657, pseudogene [Source:HGNC Symbol;Acc:HGNC:46673]"}, {"versioned_ensembl_gene_id":"ENSG00000199246.1","gene_symbol":"RNU6-896P","gene_name":"RNA, U6 small nuclear 896, pseudogene [Source:HGNC Symbol;Acc:HGNC:47859]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481922","summary":null,"start":153681447,"end":153681553,"strand":1,"description":"RNA, U6 small nuclear 896, pseudogene [Source:HGNC Symbol;Acc:HGNC:47859]"}, {"versioned_ensembl_gene_id":"ENSG00000202468.1","gene_symbol":"RNU4-17P","gene_name":"RNA, U4 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:46953]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481177","summary":null,"start":60163567,"end":60163707,"strand":1,"description":"RNA, U4 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:46953]"}, {"versioned_ensembl_gene_id":"ENSG00000207481.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41303237,"end":41303337,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200446.1","gene_symbol":"RNU6-1085P","gene_name":"RNA, U6 small nuclear 1085, pseudogene [Source:HGNC Symbol;Acc:HGNC:48048]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480043","summary":null,"start":35930158,"end":35930264,"strand":-1,"description":"RNA, U6 small nuclear 1085, pseudogene [Source:HGNC Symbol;Acc:HGNC:48048]"}, {"versioned_ensembl_gene_id":"ENSG00000202498.1","gene_symbol":"SNORD116","gene_name":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":215630026,"end":215630117,"strand":-1,"description":"Small nucleolar RNA SNORD116 [Source:RFAM;Acc:RF00108]"}, {"versioned_ensembl_gene_id":"ENSG00000252696.1","gene_symbol":"RNA5SP34","gene_name":"RNA, 5S ribosomal pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:42610]","synonyms":"RN5S34","biotype":"rRNA","ncbi_id":"100873366","summary":null,"start":90135712,"end":90135841,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:42610]"}, {"versioned_ensembl_gene_id":"ENSG00000199514.1","gene_symbol":"RNU6-235P","gene_name":"RNA, U6 small nuclear 235, pseudogene [Source:HGNC Symbol;Acc:HGNC:47198]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479671","summary":null,"start":38303773,"end":38303879,"strand":-1,"description":"RNA, U6 small nuclear 235, pseudogene [Source:HGNC Symbol;Acc:HGNC:47198]"}, {"versioned_ensembl_gene_id":"ENSG00000199203.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":210265963,"end":210266074,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265326.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition 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{"versioned_ensembl_gene_id":"ENSG00000201640.2","gene_symbol":"RN7SKP28","gene_name":"RNA, 7SK small nuclear pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:45752]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479107","summary":null,"start":96348734,"end":96349038,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:45752]"}, {"versioned_ensembl_gene_id":"ENSG00000199552.1","gene_symbol":"SNORA63","gene_name":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]","synonyms":"SNORA63A,RNE3,E3,RNU107,E3-2","biotype":"snoRNA","ncbi_id":"6043","summary":null,"start":40654963,"end":40655094,"strand":1,"description":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]"}, {"versioned_ensembl_gene_id":"ENSG00000275664.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8205851,"end":8205940,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000269103.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49932795,"end":49933078,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252133.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":62358191,"end":62358285,"strand":-1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000222122.1","gene_symbol":"RNU6-648P","gene_name":"RNA, U6 small nuclear 648, pseudogene [Source:HGNC Symbol;Acc:HGNC:47611]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479853","summary":null,"start":115032427,"end":115032533,"strand":1,"description":"RNA, U6 small nuclear 648, pseudogene [Source:HGNC Symbol;Acc:HGNC:47611]"}, {"versioned_ensembl_gene_id":"ENSG00000212396.1","gene_symbol":"RNA5SP323","gene_name":"RNA, 5S ribosomal pseudogene 323 [Source:HGNC Symbol;Acc:HGNC:43223]","synonyms":"RN5S323","biotype":"rRNA","ncbi_id":"100873589","summary":null,"start":93510548,"end":93510680,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 323 [Source:HGNC Symbol;Acc:HGNC:43223]"}, {"versioned_ensembl_gene_id":"ENSG00000257643.1","gene_symbol":"AC084824.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32692504,"end":32692848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274060.1","gene_symbol":"MIR6724-2","gene_name":"microRNA 6724-2 [Source:HGNC Symbol;Acc:HGNC:50832]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504727","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8249505,"end":8249596,"strand":1,"description":"microRNA 6724-2 [Source:HGNC Symbol;Acc:HGNC:50832]"}, {"versioned_ensembl_gene_id":"ENSG00000252224.1","gene_symbol":"RNU4ATAC15P","gene_name":"RNA, U4atac small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:46901]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479544","summary":null,"start":33174170,"end":33174295,"strand":1,"description":"RNA, U4atac small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:46901]"}, {"versioned_ensembl_gene_id":"ENSG00000284550.1","gene_symbol":"MIR8069-1","gene_name":"microRNA 8069-1 [Source:HGNC Symbol;Acc:HGNC:50262]","synonyms":"hsa-mir-8069,MIR8069","biotype":"miRNA","ncbi_id":"102466252","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6859171,"end":6859256,"strand":1,"description":"microRNA 8069-1 [Source:HGNC Symbol;Acc:HGNC:50262]"}, {"versioned_ensembl_gene_id":"ENSG00000207439.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":65123369,"end":65123474,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239190.1","gene_symbol":"RNU6-717P","gene_name":"RNA, U6 small nuclear 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:47680]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479884","summary":null,"start":133238335,"end":133238438,"strand":-1,"description":"RNA, U6 small nuclear 717, pseudogene [Source:HGNC Symbol;Acc:HGNC:47680]"}, {"versioned_ensembl_gene_id":"ENSG00000274034.1","gene_symbol":"MIR6813","gene_name":"microRNA 6813 [Source:HGNC Symbol;Acc:HGNC:50017]","synonyms":"hsa-mir-6813","biotype":"miRNA","ncbi_id":"102466741","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64076955,"end":64077010,"strand":-1,"description":"microRNA 6813 [Source:HGNC Symbol;Acc:HGNC:50017]"}, {"versioned_ensembl_gene_id":"ENSG00000277567.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868910,"end":54869016,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207292.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":149631437,"end":149631549,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263937.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28916461,"end":28916560,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000238704.1","gene_symbol":"RNU7-97P","gene_name":"RNA, U7 small nuclear 97 pseudogene [Source:HGNC Symbol;Acc:HGNC:45631]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479063","summary":null,"start":42440198,"end":42440259,"strand":-1,"description":"RNA, U7 small nuclear 97 pseudogene [Source:HGNC Symbol;Acc:HGNC:45631]"}, {"versioned_ensembl_gene_id":"ENSG00000208004.2","gene_symbol":"MIR323B","gene_name":"microRNA 323b [Source:HGNC Symbol;Acc:HGNC:38349]","synonyms":"MIRN453,MIR453,hsa-mir-453,hsa-mir-323b","biotype":"miRNA","ncbi_id":"574410","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101056219,"end":101056300,"strand":1,"description":"microRNA 323b [Source:HGNC Symbol;Acc:HGNC:38349]"}, {"versioned_ensembl_gene_id":"ENSG00000263742.1","gene_symbol":"MIR3165","gene_name":"microRNA 3165 [Source:HGNC Symbol;Acc:HGNC:38335]","synonyms":"hsa-mir-3165","biotype":"miRNA","ncbi_id":"100422953","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72072228,"end":72072302,"strand":-1,"description":"microRNA 3165 [Source:HGNC Symbol;Acc:HGNC:38335]"}, {"versioned_ensembl_gene_id":"ENSG00000276628.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000200902.1","gene_symbol":"RNU6-627P","gene_name":"RNA, U6 small nuclear 627, pseudogene [Source:HGNC Symbol;Acc:HGNC:47590]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480596","summary":null,"start":163288995,"end":163289096,"strand":1,"description":"RNA, U6 small nuclear 627, pseudogene [Source:HGNC Symbol;Acc:HGNC:47590]"}, {"versioned_ensembl_gene_id":"ENSG00000206590.1","gene_symbol":"RNU6-132P","gene_name":"RNA, U6 small nuclear 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:47095]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481219","summary":null,"start":89714232,"end":89714338,"strand":1,"description":"RNA, U6 small nuclear 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:47095]"}, {"versioned_ensembl_gene_id":"ENSG00000273610.1","gene_symbol":"RN7SL386P","gene_name":"RNA, 7SL, cytoplasmic 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:46402]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479364","summary":null,"start":21987481,"end":21987777,"strand":1,"description":"RNA, 7SL, cytoplasmic 386, pseudogene [Source:HGNC Symbol;Acc:HGNC:46402]"}, {"versioned_ensembl_gene_id":"ENSG00000276345.1","gene_symbol":"AC004556.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2585,"end":11802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263988.2","gene_symbol":"RN7SL147P","gene_name":"RNA, 7SL, cytoplasmic 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:46163]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479274","summary":null,"start":11952788,"end":11953085,"strand":-1,"description":"RNA, 7SL, cytoplasmic 147, pseudogene [Source:HGNC Symbol;Acc:HGNC:46163]"}, {"versioned_ensembl_gene_id":"ENSG00000263993.2","gene_symbol":"RN7SL786P","gene_name":"RNA, 7SL, cytoplasmic 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:46802]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479506","summary":null,"start":75742129,"end":75742426,"strand":1,"description":"RNA, 7SL, cytoplasmic 786, pseudogene [Source:HGNC Symbol;Acc:HGNC:46802]"}, {"versioned_ensembl_gene_id":"ENSG00000199165.3","gene_symbol":"MIRLET7A1","gene_name":"microRNA let-7a-1 [Source:HGNC Symbol;Acc:HGNC:31476]","synonyms":"MIRNLET7A1,hsa-let-7a-1","biotype":"miRNA","ncbi_id":"406881","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94175957,"end":94176036,"strand":1,"description":"microRNA let-7a-1 [Source:HGNC Symbol;Acc:HGNC:31476]"}, {"versioned_ensembl_gene_id":"ENSG00000207737.1","gene_symbol":"MIR181B2","gene_name":"microRNA 181b-2 [Source:HGNC Symbol;Acc:HGNC:31551]","synonyms":"hsa-mir-181b-2,MIRN181B2","biotype":"miRNA","ncbi_id":"406956","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124693710,"end":124693798,"strand":1,"description":"microRNA 181b-2 [Source:HGNC Symbol;Acc:HGNC:31551]"}, {"versioned_ensembl_gene_id":"ENSG00000284412.1","gene_symbol":"MIR4649","gene_name":"microRNA 4649 [Source:HGNC Symbol;Acc:HGNC:41852]","synonyms":"hsa-mir-4649","biotype":"miRNA","ncbi_id":"100616346","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44110849,"end":44110912,"strand":1,"description":"microRNA 4649 [Source:HGNC Symbol;Acc:HGNC:41852]"}, {"versioned_ensembl_gene_id":"ENSG00000265423.1","gene_symbol":"MIR4652","gene_name":"microRNA 4652 [Source:HGNC Symbol;Acc:HGNC:41615]","synonyms":"hsa-mir-4652","biotype":"miRNA","ncbi_id":"100616206","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93716928,"end":93717005,"strand":1,"description":"microRNA 4652 [Source:HGNC Symbol;Acc:HGNC:41615]"}, {"versioned_ensembl_gene_id":"ENSG00000200769.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":92202243,"end":92202334,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284583.1","gene_symbol":"MIR935","gene_name":"microRNA 935 [Source:HGNC Symbol;Acc:HGNC:33678]","synonyms":"MIRN935,hsa-mir-935","biotype":"miRNA","ncbi_id":"100126325","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53982307,"end":53982397,"strand":1,"description":"microRNA 935 [Source:HGNC Symbol;Acc:HGNC:33678]"}, {"versioned_ensembl_gene_id":"ENSG00000276787.1","gene_symbol":"FAN1","gene_name":"FANCD2 and FANCI associated nuclease 1 [Source:HGNC Symbol;Acc:HGNC:29170]","synonyms":"MTMR15,KIAA1018,MTMR15,KIAA1018","biotype":"protein_coding","ncbi_id":"22909","summary":"This gene plays a role in DNA interstrand cross-link repair and encodes a protein with 5' flap endonuclease and 5'-3' exonuclease activity. Mutations in this gene cause karyomegalic interstitial nephritis. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Feb 2016]","start":31055318,"end":31094547,"strand":1,"description":"FANCD2 and FANCI associated nuclease 1 [Source:HGNC Symbol;Acc:HGNC:29170]"}, {"versioned_ensembl_gene_id":"ENSG00000207347.1","gene_symbol":"RNU6-306P","gene_name":"RNA, U6 small nuclear 306, pseudogene [Source:HGNC Symbol;Acc:HGNC:47269]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479703","summary":null,"start":21564471,"end":21564577,"strand":-1,"description":"RNA, U6 small nuclear 306, pseudogene [Source:HGNC Symbol;Acc:HGNC:47269]"}, {"versioned_ensembl_gene_id":"ENSG00000239748.3","gene_symbol":"RN7SL795P","gene_name":"RNA, 7SL, cytoplasmic 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:46811]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479511","summary":null,"start":70512727,"end":70513008,"strand":1,"description":"RNA, 7SL, cytoplasmic 795, pseudogene [Source:HGNC Symbol;Acc:HGNC:46811]"}, {"versioned_ensembl_gene_id":"ENSG00000266740.1","gene_symbol":"MIR4708","gene_name":"microRNA 4708 [Source:HGNC Symbol;Acc:HGNC:41824]","synonyms":"hsa-mir-4708","biotype":"miRNA","ncbi_id":"100616176","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65335117,"end":65335183,"strand":-1,"description":"microRNA 4708 [Source:HGNC Symbol;Acc:HGNC:41824]"}, {"versioned_ensembl_gene_id":"ENSG00000207319.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206701065,"end":206701185,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199090.1","gene_symbol":"MIR326","gene_name":"microRNA 326 [Source:HGNC Symbol;Acc:HGNC:31769]","synonyms":"MIRN326,hsa-mir-326","biotype":"miRNA","ncbi_id":"442900","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75335092,"end":75335186,"strand":-1,"description":"microRNA 326 [Source:HGNC Symbol;Acc:HGNC:31769]"}, {"versioned_ensembl_gene_id":"ENSG00000212237.1","gene_symbol":"RNA5SP18","gene_name":"RNA, 5S ribosomal pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42586]","synonyms":"RN5S18","biotype":"rRNA","ncbi_id":"100873273","summary":null,"start":228647912,"end":228648032,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42586]"}, {"versioned_ensembl_gene_id":"ENSG00000274266.1","gene_symbol":"SNORA73A","gene_name":"small nucleolar RNA, H/ACA box 73A [Source:HGNC Symbol;Acc:HGNC:10115]","synonyms":"U17A,RNU17A,RNE1,E1b,E1-7,E1","biotype":"snoRNA","ncbi_id":"6080","summary":null,"start":28507366,"end":28507571,"strand":1,"description":"small nucleolar RNA, H/ACA box 73A [Source:HGNC Symbol;Acc:HGNC:10115]"}, {"versioned_ensembl_gene_id":"ENSG00000207440.1","gene_symbol":"RNU6-541P","gene_name":"RNA, U6 small nuclear 541, pseudogene [Source:HGNC Symbol;Acc:HGNC:47504]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481352","summary":null,"start":31142939,"end":31143048,"strand":1,"description":"RNA, U6 small nuclear 541, pseudogene [Source:HGNC Symbol;Acc:HGNC:47504]"}, {"versioned_ensembl_gene_id":"ENSG00000240202.3","gene_symbol":"RN7SL223P","gene_name":"RNA, 7SL, cytoplasmic 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:46239]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481754","summary":null,"start":93556913,"end":93557206,"strand":1,"description":"RNA, 7SL, cytoplasmic 223, pseudogene [Source:HGNC Symbol;Acc:HGNC:46239]"}, {"versioned_ensembl_gene_id":"ENSG00000239152.1","gene_symbol":"RNA5SP310","gene_name":"RNA, 5S ribosomal pseudogene 310 [Source:HGNC Symbol;Acc:HGNC:43210]","synonyms":"RNA5SP316,RN5S316,RN5S310","biotype":"rRNA","ncbi_id":"106480762","summary":null,"start":45856307,"end":45856422,"strand":1,"description":"RNA, 5S ribosomal pseudogene 310 [Source:HGNC Symbol;Acc:HGNC:43210]"}, {"versioned_ensembl_gene_id":"ENSG00000199698.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23432181,"end":23432282,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274164.1","gene_symbol":"RNA5SP439","gene_name":"RNA, 5S ribosomal pseudogene 439 [Source:HGNC Symbol;Acc:HGNC:43339]","synonyms":"RN5S439","biotype":"rRNA","ncbi_id":"106479014","summary":null,"start":36491199,"end":36491322,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 439 [Source:HGNC Symbol;Acc:HGNC:43339]"}, {"versioned_ensembl_gene_id":"ENSG00000278498.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":103027336,"end":103027498,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000200471.1","gene_symbol":"RNU6-1125P","gene_name":"RNA, U6 small nuclear 1125, pseudogene [Source:HGNC Symbol;Acc:HGNC:48088]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480061","summary":null,"start":54621025,"end":54621131,"strand":1,"description":"RNA, U6 small nuclear 1125, pseudogene [Source:HGNC Symbol;Acc:HGNC:48088]"}, {"versioned_ensembl_gene_id":"ENSG00000201129.1","gene_symbol":"SNORA58B","gene_name":"small nucleolar RNA, H/ACA box 58B [Source:HGNC Symbol;Acc:HGNC:52208]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617023","summary":null,"start":154259727,"end":154259862,"strand":1,"description":"small nucleolar RNA, H/ACA box 58B [Source:HGNC Symbol;Acc:HGNC:52208]"}, {"versioned_ensembl_gene_id":"ENSG00000207691.1","gene_symbol":"MIR183","gene_name":"microRNA 183 [Source:HGNC Symbol;Acc:HGNC:31554]","synonyms":"MIRN183,hsa-mir-183","biotype":"miRNA","ncbi_id":"406959","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129774905,"end":129775014,"strand":-1,"description":"microRNA 183 [Source:HGNC Symbol;Acc:HGNC:31554]"}, {"versioned_ensembl_gene_id":"ENSG00000274494.1","gene_symbol":"MIR6832","gene_name":"microRNA 6832 [Source:HGNC Symbol;Acc:HGNC:50140]","synonyms":"hsa-mir-6832","biotype":"miRNA","ncbi_id":"102466745","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31633787,"end":31633858,"strand":1,"description":"microRNA 6832 [Source:HGNC Symbol;Acc:HGNC:50140]"}, {"versioned_ensembl_gene_id":"ENSG00000272474.1","gene_symbol":"SNORD113-5","gene_name":"small nucleolar RNA, C/D box 113-5 [Source:HGNC Symbol;Acc:HGNC:32984]","synonyms":"14q(I-5)","biotype":"snoRNA","ncbi_id":"767565","summary":null,"start":100938187,"end":100938264,"strand":1,"description":"small nucleolar RNA, C/D box 113-5 [Source:HGNC Symbol;Acc:HGNC:32984]"}, {"versioned_ensembl_gene_id":"ENSG00000199545.1","gene_symbol":"RNA5SP195","gene_name":"RNA, 5S ribosomal pseudogene 195 [Source:HGNC Symbol;Acc:HGNC:43095]","synonyms":"RN5S195","biotype":"rRNA","ncbi_id":"100873457","summary":null,"start":139299852,"end":139299968,"strand":1,"description":"RNA, 5S ribosomal pseudogene 195 [Source:HGNC Symbol;Acc:HGNC:43095]"}, {"versioned_ensembl_gene_id":"ENSG00000221498.1","gene_symbol":"SNORA77","gene_name":"Small nucleolar RNA SNORA77 [Source:RFAM;Acc:RF00599]","synonyms":"SNORA77A,ACA63","biotype":"snoRNA","ncbi_id":"677843","summary":null,"start":183064235,"end":183064346,"strand":-1,"description":"Small nucleolar RNA SNORA77 [Source:RFAM;Acc:RF00599]"}, {"versioned_ensembl_gene_id":"ENSG00000203492.4","gene_symbol":"AL645937.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137410,"end":29142934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284567.1","gene_symbol":"MIR223","gene_name":"microRNA 223 [Source:HGNC Symbol;Acc:HGNC:31603]","synonyms":"MIRN223,hsa-mir-223","biotype":"miRNA","ncbi_id":"407008","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66018870,"end":66018979,"strand":1,"description":"microRNA 223 [Source:HGNC Symbol;Acc:HGNC:31603]"}, {"versioned_ensembl_gene_id":"ENSG00000264395.1","gene_symbol":"MIR3193","gene_name":"microRNA 3193 [Source:HGNC Symbol;Acc:HGNC:38204]","synonyms":"hsa-mir-3193","biotype":"miRNA","ncbi_id":"100422904","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31607186,"end":31607240,"strand":1,"description":"microRNA 3193 [Source:HGNC Symbol;Acc:HGNC:38204]"}, {"versioned_ensembl_gene_id":"ENSG00000207943.1","gene_symbol":"MIR634","gene_name":"microRNA 634 [Source:HGNC Symbol;Acc:HGNC:32890]","synonyms":"MIRN634,hsa-mir-634","biotype":"miRNA","ncbi_id":"693219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66787072,"end":66787168,"strand":1,"description":"microRNA 634 [Source:HGNC Symbol;Acc:HGNC:32890]"}, {"versioned_ensembl_gene_id":"ENSG00000207933.3","gene_symbol":"MIR9-1","gene_name":"microRNA 9-1 [Source:HGNC Symbol;Acc:HGNC:31641]","synonyms":"MIRN9-1,hsa-mir-9-1","biotype":"miRNA","ncbi_id":"407046","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":156420341,"end":156420429,"strand":-1,"description":"microRNA 9-1 [Source:HGNC Symbol;Acc:HGNC:31641]"}, {"versioned_ensembl_gene_id":"ENSG00000278113.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72567213,"end":72567380,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000206617.1","gene_symbol":"RNY1P5","gene_name":"RNA, Ro-associated Y1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42482]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862667","summary":null,"start":74289100,"end":74289214,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42482]"}, {"versioned_ensembl_gene_id":"ENSG00000207145.1","gene_symbol":"SNORA18","gene_name":"small nucleolar RNA, H/ACA box 18 [Source:HGNC Symbol;Acc:HGNC:32608]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":93733466,"end":93733597,"strand":-1,"description":"small nucleolar RNA, H/ACA box 18 [Source:HGNC Symbol;Acc:HGNC:32608]"}, {"versioned_ensembl_gene_id":"ENSG00000242101.3","gene_symbol":"RN7SL416P","gene_name":"RNA, 7SL, cytoplasmic 416, pseudogene [Source:HGNC Symbol;Acc:HGNC:46432]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481037","summary":null,"start":100530362,"end":100530659,"strand":-1,"description":"RNA, 7SL, cytoplasmic 416, pseudogene [Source:HGNC Symbol;Acc:HGNC:46432]"}, {"versioned_ensembl_gene_id":"ENSG00000221040.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":116278606,"end":116278821,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000207095.1","gene_symbol":"RNU6-424P","gene_name":"RNA, U6 small nuclear 424, pseudogene [Source:HGNC Symbol;Acc:HGNC:47387]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479753","summary":null,"start":27693731,"end":27693835,"strand":1,"description":"RNA, U6 small nuclear 424, pseudogene [Source:HGNC Symbol;Acc:HGNC:47387]"}, {"versioned_ensembl_gene_id":"ENSG00000201502.1","gene_symbol":"SNORD74","gene_name":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]","synonyms":null,"biotype":"snoRNA","ncbi_id":"619498","summary":null,"start":93266017,"end":93266096,"strand":1,"description":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]"}, {"versioned_ensembl_gene_id":"ENSG00000206601.1","gene_symbol":"RNU6-431P","gene_name":"RNA, U6 small nuclear 431, pseudogene [Source:HGNC Symbol;Acc:HGNC:47394]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481314","summary":null,"start":108652150,"end":108652256,"strand":1,"description":"RNA, U6 small nuclear 431, pseudogene [Source:HGNC Symbol;Acc:HGNC:47394]"}, {"versioned_ensembl_gene_id":"ENSG00000283728.1","gene_symbol":"MIR7108","gene_name":"microRNA 7108 [Source:HGNC Symbol;Acc:HGNC:49998]","synonyms":"hsa-mir-7108","biotype":"miRNA","ncbi_id":"102466806","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2434914,"end":2435000,"strand":-1,"description":"microRNA 7108 [Source:HGNC Symbol;Acc:HGNC:49998]"}, {"versioned_ensembl_gene_id":"ENSG00000201761.1","gene_symbol":"RNU6-336P","gene_name":"RNA, U6 small nuclear 336, pseudogene [Source:HGNC Symbol;Acc:HGNC:47299]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481285","summary":null,"start":22434391,"end":22434497,"strand":1,"description":"RNA, U6 small nuclear 336, pseudogene [Source:HGNC Symbol;Acc:HGNC:47299]"}, {"versioned_ensembl_gene_id":"ENSG00000227448.1","gene_symbol":"CR388415.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29124218,"end":29128916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211568.1","gene_symbol":"MIR670","gene_name":"microRNA 670 [Source:HGNC Symbol;Acc:HGNC:37304]","synonyms":"hsa-mir-670","biotype":"miRNA","ncbi_id":"100313777","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43559656,"end":43559753,"strand":1,"description":"microRNA 670 [Source:HGNC Symbol;Acc:HGNC:37304]"}, {"versioned_ensembl_gene_id":"ENSG00000222982.1","gene_symbol":"RN7SKP216","gene_name":"RNA, 7SK small nuclear pseudogene 216 [Source:HGNC Symbol;Acc:HGNC:45940]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479190","summary":null,"start":114504876,"end":114505187,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 216 [Source:HGNC Symbol;Acc:HGNC:45940]"}, {"versioned_ensembl_gene_id":"ENSG00000207583.1","gene_symbol":"MIR606","gene_name":"microRNA 606 [Source:HGNC Symbol;Acc:HGNC:32862]","synonyms":"MIRN606,hsa-mir-606","biotype":"miRNA","ncbi_id":"693191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75552458,"end":75552553,"strand":1,"description":"microRNA 606 [Source:HGNC Symbol;Acc:HGNC:32862]"}, {"versioned_ensembl_gene_id":"ENSG00000221673.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":219962652,"end":219962865,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000238382.1","gene_symbol":"RNU6-1211P","gene_name":"RNA, U6 small nuclear 1211, pseudogene [Source:HGNC Symbol;Acc:HGNC:48174]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480096","summary":null,"start":232700204,"end":232700308,"strand":1,"description":"RNA, U6 small nuclear 1211, pseudogene [Source:HGNC Symbol;Acc:HGNC:48174]"}, {"versioned_ensembl_gene_id":"ENSG00000222317.1","gene_symbol":"RNA5SP118","gene_name":"RNA, 5S ribosomal pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:42916]","synonyms":"RN5S118","biotype":"rRNA","ncbi_id":"100873388","summary":null,"start":209721913,"end":209722021,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 118 [Source:HGNC Symbol;Acc:HGNC:42916]"}, {"versioned_ensembl_gene_id":"ENSG00000252608.1","gene_symbol":"RNU6-1191P","gene_name":"RNA, U6 small nuclear 1191, pseudogene [Source:HGNC Symbol;Acc:HGNC:48154]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481555","summary":null,"start":81106533,"end":81106639,"strand":-1,"description":"RNA, U6 small nuclear 1191, pseudogene [Source:HGNC Symbol;Acc:HGNC:48154]"}, {"versioned_ensembl_gene_id":"ENSG00000283256.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31366288,"end":31366366,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000202224.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2621090,"end":2621201,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206896.1","gene_symbol":"RNU6-1124P","gene_name":"RNA, U6 small nuclear 1124, pseudogene [Source:HGNC Symbol;Acc:HGNC:48087]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481534","summary":null,"start":42174279,"end":42174385,"strand":-1,"description":"RNA, U6 small nuclear 1124, pseudogene [Source:HGNC Symbol;Acc:HGNC:48087]"}, {"versioned_ensembl_gene_id":"ENSG00000223076.1","gene_symbol":"RNA5SP31","gene_name":"RNA, 5S ribosomal pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42607]","synonyms":"RN5S31","biotype":"rRNA","ncbi_id":"100873363","summary":null,"start":60613608,"end":60613734,"strand":1,"description":"RNA, 5S ribosomal pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42607]"}, {"versioned_ensembl_gene_id":"ENSG00000240317.3","gene_symbol":"RN7SL764P","gene_name":"RNA, 7SL, cytoplasmic 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:46780]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480531","summary":null,"start":219102434,"end":219102719,"strand":1,"description":"RNA, 7SL, cytoplasmic 764, pseudogene [Source:HGNC Symbol;Acc:HGNC:46780]"}, {"versioned_ensembl_gene_id":"ENSG00000202383.1","gene_symbol":"RNA5SP279","gene_name":"RNA, 5S ribosomal pseudogene 279 [Source:HGNC Symbol;Acc:HGNC:43179]","synonyms":"RN5S279","biotype":"rRNA","ncbi_id":"100873532","summary":null,"start":1333837,"end":1333953,"strand":1,"description":"RNA, 5S ribosomal pseudogene 279 [Source:HGNC Symbol;Acc:HGNC:43179]"}, {"versioned_ensembl_gene_id":"ENSG00000277129.1","gene_symbol":"AC012531.5","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":53968351,"end":53968501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207156.1","gene_symbol":"RNU6-505P","gene_name":"RNA, U6 small nuclear 505, pseudogene [Source:HGNC Symbol;Acc:HGNC:47468]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479790","summary":null,"start":146996607,"end":146996713,"strand":-1,"description":"RNA, U6 small nuclear 505, pseudogene [Source:HGNC Symbol;Acc:HGNC:47468]"}, {"versioned_ensembl_gene_id":"ENSG00000266185.2","gene_symbol":"RN7SL804P","gene_name":"RNA, 7SL, cytoplasmic 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:46820]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481140","summary":null,"start":69400903,"end":69401200,"strand":1,"description":"RNA, 7SL, cytoplasmic 804, pseudogene [Source:HGNC Symbol;Acc:HGNC:46820]"}, {"versioned_ensembl_gene_id":"ENSG00000274357.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45732082,"end":45732356,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284336.1","gene_symbol":"MIR2277","gene_name":"microRNA 2277 [Source:HGNC Symbol;Acc:HGNC:37314]","synonyms":"hsa-mir-2277","biotype":"miRNA","ncbi_id":"100313887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93620696,"end":93620788,"strand":-1,"description":"microRNA 2277 [Source:HGNC Symbol;Acc:HGNC:37314]"}, {"versioned_ensembl_gene_id":"ENSG00000216009.3","gene_symbol":"MIR874","gene_name":"microRNA 874 [Source:HGNC Symbol;Acc:HGNC:33643]","synonyms":"MIRN874,hsa-mir-874","biotype":"miRNA","ncbi_id":"100126343","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":137647572,"end":137647649,"strand":-1,"description":"microRNA 874 [Source:HGNC Symbol;Acc:HGNC:33643]"}, {"versioned_ensembl_gene_id":"ENSG00000229179.1","gene_symbol":"CR388407.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076581,"end":29077176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275836.1","gene_symbol":"MIR6068","gene_name":"microRNA 6068 [Source:HGNC Symbol;Acc:HGNC:50261]","synonyms":"hsa-mir-6068","biotype":"miRNA","ncbi_id":"102464823","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63326925,"end":63326984,"strand":-1,"description":"microRNA 6068 [Source:HGNC Symbol;Acc:HGNC:50261]"}, {"versioned_ensembl_gene_id":"ENSG00000277088.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000206604.1","gene_symbol":"RNU6-425P","gene_name":"RNA, U6 small nuclear 425, pseudogene [Source:HGNC Symbol;Acc:HGNC:47388]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481312","summary":null,"start":142145454,"end":142145555,"strand":1,"description":"RNA, U6 small nuclear 425, pseudogene [Source:HGNC Symbol;Acc:HGNC:47388]"}, {"versioned_ensembl_gene_id":"ENSG00000206791.1","gene_symbol":"RNU1-129P","gene_name":"RNA, U1 small nuclear 129, pseudogene [Source:HGNC Symbol;Acc:HGNC:48471]","synonyms":"RNU1-137P","biotype":"snRNA","ncbi_id":"106481630","summary":null,"start":148014417,"end":148014583,"strand":-1,"description":"RNA, U1 small nuclear 129, pseudogene [Source:HGNC Symbol;Acc:HGNC:48471]"}, {"versioned_ensembl_gene_id":"ENSG00000252034.1","gene_symbol":"RNY4P37","gene_name":"RNA, Ro-associated Y4 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:50885]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480314","summary":null,"start":46077004,"end":46077099,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:50885]"}, {"versioned_ensembl_gene_id":"ENSG00000199787.1","gene_symbol":"SNORA80C","gene_name":"small nucleolar RNA, H/ACA box 80C [Source:HGNC Symbol;Acc:HGNC:50434]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616959","summary":null,"start":30419625,"end":30419759,"strand":-1,"description":"small nucleolar RNA, H/ACA box 80C [Source:HGNC Symbol;Acc:HGNC:50434]"}, {"versioned_ensembl_gene_id":"ENSG00000212176.1","gene_symbol":"RNA5SP207","gene_name":"RNA, 5S ribosomal pseudogene 207 [Source:HGNC Symbol;Acc:HGNC:43107]","synonyms":"RN5S207","biotype":"rRNA","ncbi_id":"100873467","summary":null,"start":41239520,"end":41239626,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 207 [Source:HGNC Symbol;Acc:HGNC:43107]"}, {"versioned_ensembl_gene_id":"ENSG00000203436.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9711953,"end":9712233,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238452.1","gene_symbol":"RNU7-144P","gene_name":"RNA, U7 small nuclear 144 pseudogene [Source:HGNC Symbol;Acc:HGNC:45678]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479079","summary":null,"start":48494234,"end":48494309,"strand":-1,"description":"RNA, U7 small nuclear 144 pseudogene [Source:HGNC Symbol;Acc:HGNC:45678]"}, {"versioned_ensembl_gene_id":"ENSG00000212363.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":74882656,"end":74882783,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000222966.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":99952033,"end":99952158,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000265319.2","gene_symbol":"RN7SL847P","gene_name":"RNA, 7SL, cytoplasmic 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:46863]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481152","summary":null,"start":33034655,"end":33034924,"strand":-1,"description":"RNA, 7SL, cytoplasmic 847, pseudogene [Source:HGNC Symbol;Acc:HGNC:46863]"}, {"versioned_ensembl_gene_id":"ENSG00000202306.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93397139,"end":93397234,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199565.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153726252,"end":153726353,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276270.1","gene_symbol":"MIR6799","gene_name":"microRNA 6799 [Source:HGNC Symbol;Acc:HGNC:50162]","synonyms":"hsa-mir-6799","biotype":"miRNA","ncbi_id":"102465479","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49791866,"end":49791934,"strand":1,"description":"microRNA 6799 [Source:HGNC Symbol;Acc:HGNC:50162]"}, {"versioned_ensembl_gene_id":"ENSG00000252563.1","gene_symbol":"RNA5SP45","gene_name":"RNA, 5S ribosomal pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:42821]","synonyms":"RN5S45","biotype":"rRNA","ncbi_id":"100873284","summary":null,"start":41466937,"end":41467028,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:42821]"}, {"versioned_ensembl_gene_id":"ENSG00000284081.1","gene_symbol":"MIR1199","gene_name":"microRNA 1199 [Source:HGNC Symbol;Acc:HGNC:50081]","synonyms":"hsa-mir-1199","biotype":"miRNA","ncbi_id":"102466515","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14073361,"end":14073479,"strand":1,"description":"microRNA 1199 [Source:HGNC Symbol;Acc:HGNC:50081]"}, {"versioned_ensembl_gene_id":"ENSG00000194297.2","gene_symbol":"RNU1-75P","gene_name":"RNA, U1 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:48417]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480172","summary":null,"start":119331397,"end":119331525,"strand":-1,"description":"RNA, U1 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:48417]"}, {"versioned_ensembl_gene_id":"ENSG00000223075.1","gene_symbol":"RN7SKP126","gene_name":"RNA, 7SK small nuclear pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:45850]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480872","summary":null,"start":192875686,"end":192875985,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:45850]"}, {"versioned_ensembl_gene_id":"ENSG00000235836.1","gene_symbol":"KIF3AP1","gene_name":"kinesin family member 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419880","summary":null,"start":195843986,"end":195844596,"strand":1,"description":"kinesin family member 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52811]"}, {"versioned_ensembl_gene_id":"ENSG00000276917.1","gene_symbol":"MIR8080","gene_name":"microRNA 8080 [Source:HGNC Symbol;Acc:HGNC:49989]","synonyms":"hsa-mir-8080","biotype":"miRNA","ncbi_id":"102465877","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":79866495,"end":79866583,"strand":-1,"description":"microRNA 8080 [Source:HGNC Symbol;Acc:HGNC:49989]"}, {"versioned_ensembl_gene_id":"ENSG00000278459.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7856169,"end":7856471,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000239390.3","gene_symbol":"RN7SL87P","gene_name":"RNA, 7SL, cytoplasmic 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:46103]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479255","summary":null,"start":144140879,"end":144141166,"strand":1,"description":"RNA, 7SL, cytoplasmic 87, pseudogene [Source:HGNC Symbol;Acc:HGNC:46103]"}, {"versioned_ensembl_gene_id":"ENSG00000251828.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":80306235,"end":80306368,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000200538.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":48382371,"end":48382586,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000199691.1","gene_symbol":"RN7SKP173","gene_name":"RNA, 7SK small nuclear pseudogene 173 [Source:HGNC Symbol;Acc:HGNC:45897]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106635535","summary":null,"start":38761528,"end":38761842,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 173 [Source:HGNC Symbol;Acc:HGNC:45897]"}, {"versioned_ensembl_gene_id":"ENSG00000251742.1","gene_symbol":"RN7SKP13","gene_name":"RNA, 7SK small nuclear pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:45737]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479100","summary":null,"start":181834865,"end":181835108,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:45737]"}, {"versioned_ensembl_gene_id":"ENSG00000221705.1","gene_symbol":"SNORA11E","gene_name":"small nucleolar RNA, H/ACA box 11E [Source:HGNC Symbol;Acc:HGNC:33623]","synonyms":null,"biotype":"snoRNA","ncbi_id":"101340250","summary":null,"start":52063347,"end":52063474,"strand":-1,"description":"small nucleolar RNA, H/ACA box 11E [Source:HGNC Symbol;Acc:HGNC:33623]"}, {"versioned_ensembl_gene_id":"ENSG00000264259.1","gene_symbol":"RNU1-116P","gene_name":"RNA, U1 small nuclear 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48458]","synonyms":null,"biotype":"snRNA","ncbi_id":"107521946","summary":null,"start":32505701,"end":32505847,"strand":-1,"description":"RNA, U1 small nuclear 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:48458]"}, {"versioned_ensembl_gene_id":"ENSG00000252770.1","gene_symbol":"RNU7-4P","gene_name":"RNA, U7 small nuclear 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:34100]","synonyms":"U7.4,RNU7-132P","biotype":"snRNA","ncbi_id":"100147747","summary":null,"start":68911921,"end":68911982,"strand":1,"description":"RNA, U7 small nuclear 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:34100]"}, {"versioned_ensembl_gene_id":"ENSG00000207012.2","gene_symbol":"RNU6-72P","gene_name":"RNA, U6 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:42562]","synonyms":"RNU6-72","biotype":"snRNA","ncbi_id":"100873775","summary":null,"start":72047873,"end":72047951,"strand":-1,"description":"RNA, U6 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:42562]"}, {"versioned_ensembl_gene_id":"ENSG00000264017.2","gene_symbol":"RN7SL336P","gene_name":"RNA, 7SL, cytoplasmic 336, pseudogene [Source:HGNC Symbol;Acc:HGNC:46352]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479346","summary":null,"start":89090946,"end":89091242,"strand":1,"description":"RNA, 7SL, cytoplasmic 336, pseudogene [Source:HGNC Symbol;Acc:HGNC:46352]"}, {"versioned_ensembl_gene_id":"ENSG00000207609.3","gene_symbol":"MIR491","gene_name":"microRNA 491 [Source:HGNC Symbol;Acc:HGNC:32076]","synonyms":"MIRN491,hsa-mir-491","biotype":"miRNA","ncbi_id":"574444","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20716105,"end":20716188,"strand":1,"description":"microRNA 491 [Source:HGNC Symbol;Acc:HGNC:32076]"}, {"versioned_ensembl_gene_id":"ENSG00000221176.1","gene_symbol":"MIR1207","gene_name":"microRNA 1207 [Source:HGNC Symbol;Acc:HGNC:35273]","synonyms":"MIRN1207,hsa-mir-1207","biotype":"miRNA","ncbi_id":"100302175","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128049152,"end":128049238,"strand":1,"description":"microRNA 1207 [Source:HGNC Symbol;Acc:HGNC:35273]"}, {"versioned_ensembl_gene_id":"ENSG00000277063.1","gene_symbol":"MIR8084","gene_name":"microRNA 8084 [Source:HGNC Symbol;Acc:HGNC:50075]","synonyms":"hsa-mir-8084","biotype":"miRNA","ncbi_id":"102467005","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93029751,"end":93029839,"strand":1,"description":"microRNA 8084 [Source:HGNC Symbol;Acc:HGNC:50075]"}, {"versioned_ensembl_gene_id":"ENSG00000251663.1","gene_symbol":"SUMO2P5","gene_name":"SUMO2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39015]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526738","summary":null,"start":75225424,"end":75225668,"strand":1,"description":"SUMO2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39015]"}, {"versioned_ensembl_gene_id":"ENSG00000249157.1","gene_symbol":"AC093259.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75006713,"end":75007012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226734.1","gene_symbol":"SNRPGP12","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874427","summary":null,"start":110139214,"end":110139426,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39331]"}, {"versioned_ensembl_gene_id":"ENSG00000261320.1","gene_symbol":"AC009061.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67430667,"end":67431464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078295.16","gene_symbol":"ADCY2","gene_name":"adenylate cyclase 2 [Source:HGNC Symbol;Acc:HGNC:233]","synonyms":"KIAA1060,HBAC2,AC2","biotype":"protein_coding","ncbi_id":"108","summary":"This gene encodes a member of the family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). This enzyme is insensitive to Ca(2+)/calmodulin, and is stimulated by the G protein beta and gamma subunit complex. [provided by RefSeq, Jul 2008]","start":7396208,"end":7830081,"strand":1,"description":"adenylate cyclase 2 [Source:HGNC Symbol;Acc:HGNC:233]"}, {"versioned_ensembl_gene_id":"ENSG00000173237.4","gene_symbol":"C11orf86","gene_name":"chromosome 11 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:34442]","synonyms":"FLJ22675","biotype":"protein_coding","ncbi_id":"254439","summary":null,"start":66975277,"end":66977004,"strand":1,"description":"chromosome 11 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:34442]"}, {"versioned_ensembl_gene_id":"ENSG00000264172.1","gene_symbol":"PDLIM1P3","gene_name":"PDZ and LIM domain 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419427","summary":null,"start":27002661,"end":27003259,"strand":-1,"description":"PDZ and LIM domain 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48946]"}, {"versioned_ensembl_gene_id":"ENSG00000263433.1","gene_symbol":"AC069061.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26981694,"end":26982090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228153.1","gene_symbol":"AL161793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204663872,"end":204664613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240710.1","gene_symbol":"AL512306.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204603035,"end":204616565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119138.4","gene_symbol":"KLF9","gene_name":"Kruppel like factor 9 [Source:HGNC Symbol;Acc:HGNC:1123]","synonyms":"BTEB1","biotype":"protein_coding","ncbi_id":"687","summary":"The protein encoded by this gene is a transcription factor that binds to GC box elements located in the promoter. Binding of the encoded protein to a single GC box inhibits mRNA expression while binding to tandemly repeated GC box elements activates transcription. [provided by RefSeq, Jul 2008]","start":70384597,"end":70414624,"strand":-1,"description":"Kruppel like factor 9 [Source:HGNC Symbol;Acc:HGNC:1123]"}, {"versioned_ensembl_gene_id":"ENSG00000265567.1","gene_symbol":"AC138761.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22301333,"end":22301657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264562.1","gene_symbol":"AC138761.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22305671,"end":22306013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260458.3","gene_symbol":"KCNJ18","gene_name":"potassium voltage-gated channel subfamily J member 18 [Source:HGNC Symbol;Acc:HGNC:39080]","synonyms":"TTPP2,KIR2.6","biotype":"protein_coding","ncbi_id":"100134444","summary":"This gene encodes a member of the inwardly rectifying potassium channel family. Transcription of this locus is regulated by thyroid hormone, and the encoded protein plays a role in resting membrane potential maintenance. Mutations in this locus have been associated with thyrotoxic hypokalemic periodic paralysis. [provided by RefSeq, Jan 2013]","start":21692523,"end":21704612,"strand":1,"description":"potassium voltage-gated channel subfamily J member 18 [Source:HGNC Symbol;Acc:HGNC:39080]"}, {"versioned_ensembl_gene_id":"ENSG00000224420.3","gene_symbol":"ADM5","gene_name":"adrenomedullin 5 (putative) [Source:HGNC Symbol;Acc:HGNC:27293]","synonyms":"C19orf76,AM5","biotype":"protein_coding","ncbi_id":"199800","summary":null,"start":49688664,"end":49690575,"strand":1,"description":"adrenomedullin 5 (putative) [Source:HGNC Symbol;Acc:HGNC:27293]"}, {"versioned_ensembl_gene_id":"ENSG00000231691.1","gene_symbol":"AL592114.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204277005,"end":204277948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197119.12","gene_symbol":"SLC25A29","gene_name":"solute carrier family 25 member 29 [Source:HGNC Symbol;Acc:HGNC:20116]","synonyms":"FLJ38975,C14orf69","biotype":"protein_coding","ncbi_id":"123096","summary":"This gene encodes a nuclear-encoded mitochondrial protein that is a member of the large family of solute carrier family 25 (SLC25) mitochondrial transporters. The members of this superfamily are involved in numerous metabolic pathways and cell functions. This gene product was previously reported to be a mitochondrial carnitine-acylcarnitine-like (CACL) translocase (PMID:128829710) or an ornithine transporter (designated ORNT3, PMID:19287344), however, a recent study characterized the main role of this protein as a mitochondrial transporter of basic amino acids, with a preference for arginine and lysine (PMID:24652292). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2014]","start":100291111,"end":100306547,"strand":-1,"description":"solute carrier family 25 member 29 [Source:HGNC Symbol;Acc:HGNC:20116]"}, {"versioned_ensembl_gene_id":"ENSG00000113119.12","gene_symbol":"TMCO6","gene_name":"transmembrane and coiled-coil domains 6 [Source:HGNC Symbol;Acc:HGNC:28814]","synonyms":"PRO1580,FLJ39769","biotype":"protein_coding","ncbi_id":"55374","summary":null,"start":140639427,"end":140645408,"strand":1,"description":"transmembrane and coiled-coil domains 6 [Source:HGNC Symbol;Acc:HGNC:28814]"}, {"versioned_ensembl_gene_id":"ENSG00000230550.1","gene_symbol":"AL592146.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":204141408,"end":204143009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235530.6","gene_symbol":"AC087294.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21214331,"end":21230035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251205.2","gene_symbol":"AC016598.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143559219,"end":143562548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257315.2","gene_symbol":"ZBED6","gene_name":"zinc finger BED-type containing 6 [Source:HGNC Symbol;Acc:HGNC:33273]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100381270","summary":"The protein encoded by this transposon-derived intronless gene is a transcriptional repressor that binds to the consensus sequence 5'-GCTCGC-3'. The encoded protein has been shown to repress IGF2 transcription. This gene is located within the first intron of the ZC3H11A gene. [provided by RefSeq, Jul 2016]","start":203795714,"end":203854999,"strand":1,"description":"zinc finger BED-type containing 6 [Source:HGNC Symbol;Acc:HGNC:33273]"}, {"versioned_ensembl_gene_id":"ENSG00000149357.9","gene_symbol":"LAMTOR1","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 [Source:HGNC Symbol;Acc:HGNC:26068]","synonyms":"Ragulator1,Pdro,p27RF-Rho,p18,FLJ20625,C11orf59","biotype":"protein_coding","ncbi_id":"55004","summary":null,"start":72085895,"end":72103387,"strand":-1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 [Source:HGNC Symbol;Acc:HGNC:26068]"}, {"versioned_ensembl_gene_id":"ENSG00000142534.6","gene_symbol":"RPS11","gene_name":"ribosomal protein S11 [Source:HGNC Symbol;Acc:HGNC:10384]","synonyms":"S11","biotype":"protein_coding","ncbi_id":"6205","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the S17P family of ribosomal proteins that is a component of the 40S subunit. This gene is co-transcribed with the small nucleolar RNA gene U35B, which is located in the third intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. [provided by RefSeq, Jul 2012]","start":49496365,"end":49499689,"strand":1,"description":"ribosomal protein S11 [Source:HGNC Symbol;Acc:HGNC:10384]"}, {"versioned_ensembl_gene_id":"ENSG00000174080.10","gene_symbol":"CTSF","gene_name":"cathepsin F [Source:HGNC Symbol;Acc:HGNC:2531]","synonyms":"CLN13,CATSF","biotype":"protein_coding","ncbi_id":"8722","summary":"Cathepsins are papain family cysteine proteinases that represent a major component of the lysosomal proteolytic system. Cathepsins generally contain a signal sequence, followed by a propeptide and then a catalytically active mature region. The very long (251 amino acid residues) proregion of the cathepsin F precursor contains a C-terminal domain similar to the pro-segment of cathepsin L-like enzymes, a 50-residue flexible linker peptide, and an N-terminal domain predicted to adopt a cystatin-like fold. The cathepsin F proregion is unique within the papain family cysteine proteases in that it contains this additional N-terminal segment predicted to share structural similarities with cysteine protease inhibitors of the cystatin superfamily. This cystatin-like domain contains some of the elements known to be important for inhibitory activity. CTSF encodes a predicted protein of 484 amino acids which contains a 19 residue signal peptide. Cathepsin F contains five potential N-glycosylation sites, and it may be targeted to the endosomal/lysosomal compartment via the mannose 6-phosphate receptor pathway. The cathepsin F gene is ubiquitously expressed, and it maps to chromosome 11q13, close to the gene encoding cathepsin W. [provided by RefSeq, Jul 2008]","start":66563463,"end":66568841,"strand":-1,"description":"cathepsin F [Source:HGNC Symbol;Acc:HGNC:2531]"}, {"versioned_ensembl_gene_id":"ENSG00000263729.1","gene_symbol":"AC087393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20983902,"end":20984046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109794.13","gene_symbol":"FAM149A","gene_name":"family with sequence similarity 149 member A [Source:HGNC Symbol;Acc:HGNC:24527]","synonyms":"MSTP119,MST119,DKFZP564J102","biotype":"protein_coding","ncbi_id":"25854","summary":null,"start":186104419,"end":186172667,"strand":1,"description":"family with sequence similarity 149 member A [Source:HGNC Symbol;Acc:HGNC:24527]"}, {"versioned_ensembl_gene_id":"ENSG00000213260.3","gene_symbol":"YWHAZP5","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30564]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"86123","summary":null,"start":105686322,"end":105687051,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30564]"}, {"versioned_ensembl_gene_id":"ENSG00000188013.6","gene_symbol":"AC087499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20589293,"end":20590367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113070.7","gene_symbol":"HBEGF","gene_name":"heparin binding EGF like growth factor [Source:HGNC Symbol;Acc:HGNC:3059]","synonyms":"HEGFL,DTS,DTR","biotype":"protein_coding","ncbi_id":"1839","summary":null,"start":140332843,"end":140346631,"strand":-1,"description":"heparin binding EGF like growth factor [Source:HGNC Symbol;Acc:HGNC:3059]"}, {"versioned_ensembl_gene_id":"ENSG00000214819.1","gene_symbol":"CDRT15L2","gene_name":"CMT1A duplicated region transcript 15 like 2 [Source:HGNC Symbol;Acc:HGNC:34075]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256223","summary":null,"start":20579724,"end":20580911,"strand":1,"description":"CMT1A duplicated region transcript 15 like 2 [Source:HGNC Symbol;Acc:HGNC:34075]"}, {"versioned_ensembl_gene_id":"ENSG00000258869.1","gene_symbol":"LINC02312","gene_name":"long intergenic non-protein coding RNA 2312 [Source:HGNC Symbol;Acc:HGNC:53231]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132612","summary":null,"start":97749264,"end":97763989,"strand":-1,"description":"long intergenic non-protein coding RNA 2312 [Source:HGNC Symbol;Acc:HGNC:53231]"}, {"versioned_ensembl_gene_id":"ENSG00000131401.11","gene_symbol":"NAPSB","gene_name":"napsin B aspartic peptidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:13396]","synonyms":"NAPSBP,NAPB,NAP2,NAP1L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"256236","summary":null,"start":50333796,"end":50344767,"strand":-1,"description":"napsin B aspartic peptidase, pseudogene [Source:HGNC Symbol;Acc:HGNC:13396]"}, {"versioned_ensembl_gene_id":"ENSG00000246084.2","gene_symbol":"LINC02325","gene_name":"long intergenic non-protein coding RNA 2325 [Source:HGNC Symbol;Acc:HGNC:53245]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929241","summary":null,"start":97458816,"end":97581601,"strand":1,"description":"long intergenic non-protein coding RNA 2325 [Source:HGNC Symbol;Acc:HGNC:53245]"}, {"versioned_ensembl_gene_id":"ENSG00000197176.7","gene_symbol":"LINC02291","gene_name":"long intergenic non-protein coding RNA 2291 [Source:HGNC Symbol;Acc:HGNC:53207]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129345","summary":null,"start":97632647,"end":97686658,"strand":-1,"description":"long intergenic non-protein coding RNA 2291 [Source:HGNC Symbol;Acc:HGNC:53207]"}, {"versioned_ensembl_gene_id":"ENSG00000148841.15","gene_symbol":"ITPRIP","gene_name":"inositol 1,4,5-trisphosphate receptor interacting protein [Source:HGNC Symbol;Acc:HGNC:29370]","synonyms":"KIAA1754,DANGER,bA127L20.2","biotype":"protein_coding","ncbi_id":"85450","summary":"This gene encodes a membrane-associated protein that binds the inositol 1,4,5-trisphosphate receptor (ITPR). The encoded protein enhances the sensitivity of ITPR to intracellular calcium signaling. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":104309698,"end":104338404,"strand":-1,"description":"inositol 1,4,5-trisphosphate receptor interacting protein [Source:HGNC Symbol;Acc:HGNC:29370]"}, {"versioned_ensembl_gene_id":"ENSG00000270075.1","gene_symbol":"AL162742.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104312141,"end":104313881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231507.1","gene_symbol":"LINC01353","gene_name":"long intergenic non-protein coding RNA 1353 [Source:HGNC Symbol;Acc:HGNC:50580]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506775","summary":null,"start":203287152,"end":203288801,"strand":1,"description":"long intergenic non-protein coding RNA 1353 [Source:HGNC Symbol;Acc:HGNC:50580]"}, {"versioned_ensembl_gene_id":"ENSG00000233791.5","gene_symbol":"LINC01136","gene_name":"long intergenic non-protein coding RNA 1136 [Source:HGNC Symbol;Acc:HGNC:49452]","synonyms":null,"biotype":"lincRNA","ncbi_id":"730227","summary":null,"start":203298758,"end":203305309,"strand":-1,"description":"long intergenic non-protein coding RNA 1136 [Source:HGNC Symbol;Acc:HGNC:49452]"}, {"versioned_ensembl_gene_id":"ENSG00000214822.8","gene_symbol":"KRT16P3","gene_name":"keratin 16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37808]","synonyms":"MGC102966,KERSMCR","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644945","summary":null,"start":20501513,"end":20512357,"strand":-1,"description":"keratin 16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37808]"}, {"versioned_ensembl_gene_id":"ENSG00000197748.12","gene_symbol":"CFAP43","gene_name":"cilia and flagella associated protein 43 [Source:HGNC Symbol;Acc:HGNC:26684]","synonyms":"WDR96,FLJ36006,FLJ22944,C10orf79,bA373N18.2","biotype":"protein_coding","ncbi_id":"80217","summary":"This gene encodes a member of the cilia- and flagella-associated protein family. [provided by RefSeq, Sep 2016]","start":104129888,"end":104232362,"strand":-1,"description":"cilia and flagella associated protein 43 [Source:HGNC Symbol;Acc:HGNC:26684]"}, {"versioned_ensembl_gene_id":"ENSG00000263976.1","gene_symbol":"YWHAEP3","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49430]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480273","summary":null,"start":20491323,"end":20491443,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49430]"}, {"versioned_ensembl_gene_id":"ENSG00000226337.3","gene_symbol":"AL353616.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68541036,"end":68644442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234506.5","gene_symbol":"LINC01506","gene_name":"long intergenic non-protein coding RNA 1506 [Source:HGNC Symbol;Acc:HGNC:51187]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927015","summary":null,"start":68543541,"end":68546589,"strand":-1,"description":"long intergenic non-protein coding RNA 1506 [Source:HGNC Symbol;Acc:HGNC:51187]"}, {"versioned_ensembl_gene_id":"ENSG00000214903.4","gene_symbol":"AL358832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47444106,"end":47444494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188389.10","gene_symbol":"PDCD1","gene_name":"programmed cell death 1 [Source:HGNC Symbol;Acc:HGNC:8760]","synonyms":"SLEB2,PD1,PD-1,hSLE1,CD279","biotype":"protein_coding","ncbi_id":"5133","summary":"Programmed cell death protein 1 (PDCD1) is an immune-inhibitory receptor expressed in activated T cells; it is involved in the regulation of T-cell functions, including those of effector CD8+ T cells. In addition, this protein can also promote the differentiation of CD4+ T cells into T regulatory cells. PDCD1 is expressed in many types of tumors including melanomas, and has demonstrated to play a role in anti-tumor immunity. Moreover, this protein has been shown to be involved in safeguarding against autoimmunity, however, it can also contribute to the inhibition of effective anti-tumor and anti-microbial immunity. [provided by RefSeq, Aug 2020]","start":241849881,"end":241858908,"strand":-1,"description":"programmed cell death 1 [Source:HGNC Symbol;Acc:HGNC:8760]"}, {"versioned_ensembl_gene_id":"ENSG00000133398.3","gene_symbol":"MED10","gene_name":"mediator complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:28760]","synonyms":"TRG20,NUT2,MGC5309,L6","biotype":"protein_coding","ncbi_id":"84246","summary":"MED10 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008]","start":6371881,"end":6378594,"strand":-1,"description":"mediator complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:28760]"}, {"versioned_ensembl_gene_id":"ENSG00000254602.1","gene_symbol":"AP000662.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":57638024,"end":57652790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132024.17","gene_symbol":"CC2D1A","gene_name":"coiled-coil and C2 domain containing 1A [Source:HGNC Symbol;Acc:HGNC:30237]","synonyms":"MRT3,FLJ20241","biotype":"protein_coding","ncbi_id":"54862","summary":"This gene encodes a transcriptional repressor that binds to a conserved 14-bp 5'-repressor element and regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA binding and transcriptional repressor activities of the protein are inhibited by calcium. A mutation in this gene results in a nonsyndromic form of cognitive disability (MRT3). [provided by RefSeq, Jul 2017]","start":13906201,"end":13930879,"strand":1,"description":"coiled-coil and C2 domain containing 1A [Source:HGNC Symbol;Acc:HGNC:30237]"}, {"versioned_ensembl_gene_id":"ENSG00000258700.5","gene_symbol":"LINC00871","gene_name":"long intergenic non-protein coding RNA 871 [Source:HGNC Symbol;Acc:HGNC:47038]","synonyms":"RP11-1A16.1","biotype":"lincRNA","ncbi_id":"100506412","summary":null,"start":45940943,"end":46501823,"strand":1,"description":"long intergenic non-protein coding RNA 871 [Source:HGNC Symbol;Acc:HGNC:47038]"}, {"versioned_ensembl_gene_id":"ENSG00000132016.11","gene_symbol":"C19orf57","gene_name":"chromosome 19 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:28153]","synonyms":"MGC11271","biotype":"protein_coding","ncbi_id":"79173","summary":null,"start":13882348,"end":13906452,"strand":-1,"description":"chromosome 19 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:28153]"}, {"versioned_ensembl_gene_id":"ENSG00000242602.1","gene_symbol":"AC008953.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72878868,"end":72879185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255377.1","gene_symbol":"DUXAP5","gene_name":"double homeobox A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32184]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503634","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":119444991,"end":119445519,"strand":-1,"description":"double homeobox A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32184]"}, {"versioned_ensembl_gene_id":"ENSG00000277159.1","gene_symbol":"AL139384.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112602828,"end":112606417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171298.12","gene_symbol":"GAA","gene_name":"glucosidase alpha, acid [Source:HGNC Symbol;Acc:HGNC:4065]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2548","summary":"This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":80101556,"end":80119879,"strand":1,"description":"glucosidase alpha, acid [Source:HGNC Symbol;Acc:HGNC:4065]"}, {"versioned_ensembl_gene_id":"ENSG00000129534.13","gene_symbol":"MIS18BP1","gene_name":"MIS18 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:20190]","synonyms":"M18BP1,KNL2,KIAA1903,FLJ11186,C14orf106","biotype":"protein_coding","ncbi_id":"55320","summary":null,"start":45203190,"end":45253540,"strand":-1,"description":"MIS18 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:20190]"}, {"versioned_ensembl_gene_id":"ENSG00000251476.2","gene_symbol":"MTCO1P31","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52096]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075171","summary":null,"start":5396477,"end":5396968,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52096]"}, {"versioned_ensembl_gene_id":"ENSG00000250808.1","gene_symbol":"MTCO2P30","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52159]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075195","summary":null,"start":5395972,"end":5396335,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52159]"}, {"versioned_ensembl_gene_id":"ENSG00000204642.13","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29722775,"end":29738528,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000267633.1","gene_symbol":"AC008686.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13772118,"end":13774118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214872.8","gene_symbol":"SMTNL1","gene_name":"smoothelin like 1 [Source:HGNC Symbol;Acc:HGNC:32394]","synonyms":"CHASM","biotype":"protein_coding","ncbi_id":"219537","summary":"The protein encoded by this gene is involved in the contraction of both striated and smooth muscle. During pregnancy, the encoded protein interacts with progesterone receptor to attenuate the expression of contractile and metabolic proteins. [provided by RefSeq, Jul 2016]","start":57542641,"end":57550274,"strand":1,"description":"smoothelin like 1 [Source:HGNC Symbol;Acc:HGNC:32394]"}, {"versioned_ensembl_gene_id":"ENSG00000113552.15","gene_symbol":"GNPDA1","gene_name":"glucosamine-6-phosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:4417]","synonyms":"KIAA0060,HLN,GPI,GNPI,GNPDA","biotype":"protein_coding","ncbi_id":"10007","summary":"Glucosamine-6-phosphate deaminase (EC 3.5.99.6) is an allosteric enzyme that catalyzes the reversible conversion of D-glucosamine-6-phosphate into D-fructose-6-phosphate and ammonium (Arreola et al., 2003 [PubMed 12965206]).[supplied by OMIM, Jan 2010]","start":141991749,"end":142013041,"strand":-1,"description":"glucosamine-6-phosphate deaminase 1 [Source:HGNC Symbol;Acc:HGNC:4417]"}, {"versioned_ensembl_gene_id":"ENSG00000233916.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29708125,"end":29708547,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000128487.16","gene_symbol":"SPECC1","gene_name":"sperm antigen with calponin homology and coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:30615]","synonyms":"FLJ36955,CYTSB,NSP,HCMOGT-1","biotype":"protein_coding","ncbi_id":"92521","summary":"The protein encoded by this gene belongs to the cytospin-A family. It is localized in the nucleus, and highly expressed in testis and some cancer cell lines. A chromosomal translocation involving this gene and platelet-derived growth factor receptor, beta gene (PDGFRB) may be a cause of juvenile myelomonocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":20009344,"end":20319026,"strand":1,"description":"sperm antigen with calponin homology and coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:30615]"}, {"versioned_ensembl_gene_id":"ENSG00000225681.2","gene_symbol":"AC005730.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20056287,"end":20056630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278012.1","gene_symbol":"AL031658.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31970181,"end":31970831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260903.2","gene_symbol":"XKR7","gene_name":"XK related 7 [Source:HGNC Symbol;Acc:HGNC:23062]","synonyms":"dJ310O13.4,C20orf159","biotype":"protein_coding","ncbi_id":"343702","summary":null,"start":31968002,"end":32003387,"strand":1,"description":"XK related 7 [Source:HGNC Symbol;Acc:HGNC:23062]"}, {"versioned_ensembl_gene_id":"ENSG00000235985.7","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"IRT-1,AIF-1,IBA1,Em:AF129756.17","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31691477,"end":31693314,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000184276.2","gene_symbol":"DEFB108B","gene_name":"defensin beta 108B [Source:HGNC Symbol;Acc:HGNC:29966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"245911","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. A pseudogene of this gene has been found on chromosome 8. [provided by RefSeq, Oct 2014]","start":71833200,"end":71837710,"strand":1,"description":"defensin beta 108B [Source:HGNC Symbol;Acc:HGNC:29966]"}, {"versioned_ensembl_gene_id":"ENSG00000260391.2","gene_symbol":"AC022336.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":124723788,"end":124726325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089902.9","gene_symbol":"RCOR1","gene_name":"REST corepressor 1 [Source:HGNC Symbol;Acc:HGNC:17441]","synonyms":"KIAA0071,COREST,RCOR","biotype":"protein_coding","ncbi_id":"23186","summary":"This gene encodes a protein that is well-conserved, downregulated at birth, and with a specific role in determining neural cell differentiation. The encoded protein binds to the C-terminal domain of REST (repressor element-1 silencing transcription factor). [provided by RefSeq, Aug 2011]","start":102592661,"end":102730576,"strand":1,"description":"REST corepressor 1 [Source:HGNC Symbol;Acc:HGNC:17441]"}, {"versioned_ensembl_gene_id":"ENSG00000226967.1","gene_symbol":"HAUS4P1","gene_name":"HAUS augmin like complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43763]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129402","summary":null,"start":170369223,"end":170370367,"strand":-1,"description":"HAUS augmin like complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43763]"}, {"versioned_ensembl_gene_id":"ENSG00000227619.1","gene_symbol":"AL391056.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129575409,"end":129584556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269540.1","gene_symbol":"AC010624.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50058882,"end":50060232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216977.1","gene_symbol":"RPL21P65","gene_name":"ribosomal protein L21 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:36017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271178","summary":null,"start":106642463,"end":106642928,"strand":1,"description":"ribosomal protein L21 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:36017]"}, {"versioned_ensembl_gene_id":"ENSG00000204666.3","gene_symbol":"AC010624.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":50050589,"end":50066793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137507.11","gene_symbol":"LRRC32","gene_name":"leucine rich repeat containing 32 [Source:HGNC Symbol;Acc:HGNC:4161]","synonyms":"GARP,D11S833E","biotype":"protein_coding","ncbi_id":"2615","summary":"This gene encodes a type I membrane protein which contains 20 leucine-rich repeats. Alterations in the chromosomal region 11q13-11q14 are involved in several pathologies. [provided by RefSeq, Jul 2008]","start":76657524,"end":76670747,"strand":-1,"description":"leucine rich repeat containing 32 [Source:HGNC Symbol;Acc:HGNC:4161]"}, {"versioned_ensembl_gene_id":"ENSG00000164574.15","gene_symbol":"GALNT10","gene_name":"polypeptide N-acetylgalactosaminyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:19873]","synonyms":"GalNAc-T10","biotype":"protein_coding","ncbi_id":"55568","summary":"This gene encodes a member of the GalNAc polypeptide N-acetylgalactosaminyltransferases. These enzymes catalyze the first step in the synthesis of mucin-type oligosaccharides. These proteins transfer GalNAc from UDP-GalNAc to either serine or threonine residues of polypeptide acceptors. The protein encoded by this locus may have increased catalytic activity toward glycosylated peptides compared to activity toward non-glycosylated peptides.[provided by RefSeq, Apr 2010]","start":154190730,"end":154420984,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:19873]"}, {"versioned_ensembl_gene_id":"ENSG00000167257.10","gene_symbol":"RNF214","gene_name":"ring finger protein 214 [Source:HGNC Symbol;Acc:HGNC:25335]","synonyms":"DKFZp547C195","biotype":"protein_coding","ncbi_id":"257160","summary":null,"start":117232625,"end":117286445,"strand":1,"description":"ring finger protein 214 [Source:HGNC Symbol;Acc:HGNC:25335]"}, {"versioned_ensembl_gene_id":"ENSG00000132681.16","gene_symbol":"ATP1A4","gene_name":"ATPase Na+/K+ transporting subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:14073]","synonyms":"ATP1AL2","biotype":"protein_coding","ncbi_id":"480","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 4 subunit. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":160151570,"end":160186977,"strand":1,"description":"ATPase Na+/K+ transporting subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:14073]"}, {"versioned_ensembl_gene_id":"ENSG00000188959.9","gene_symbol":"C9orf152","gene_name":"chromosome 9 open reading frame 152 [Source:HGNC Symbol;Acc:HGNC:31455]","synonyms":"bA470J20.2","biotype":"protein_coding","ncbi_id":"401546","summary":null,"start":110190048,"end":110208189,"strand":-1,"description":"chromosome 9 open reading frame 152 [Source:HGNC Symbol;Acc:HGNC:31455]"}, {"versioned_ensembl_gene_id":"ENSG00000215231.7","gene_symbol":"LINC01020","gene_name":"long intergenic non-protein coding RNA 1020 [Source:HGNC Symbol;Acc:HGNC:27968]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340094","summary":null,"start":5034359,"end":5070004,"strand":1,"description":"long intergenic non-protein coding RNA 1020 [Source:HGNC Symbol;Acc:HGNC:27968]"}, {"versioned_ensembl_gene_id":"ENSG00000155324.9","gene_symbol":"GRAMD2B","gene_name":"GRAM domain containing 2B [Source:HGNC Symbol;Acc:HGNC:24911]","synonyms":"NS3TP2,GRAMD3,FLJ21313","biotype":"protein_coding","ncbi_id":"65983","summary":null,"start":126360132,"end":126496494,"strand":1,"description":"GRAM domain containing 2B [Source:HGNC Symbol;Acc:HGNC:24911]"}, {"versioned_ensembl_gene_id":"ENSG00000161929.14","gene_symbol":"SCIMP","gene_name":"SLP adaptor and CSK interacting membrane protein [Source:HGNC Symbol;Acc:HGNC:33504]","synonyms":"UNQ5783,MGC163428,MGC163426,FLJ32580,DTFT5783,C17orf87","biotype":"protein_coding","ncbi_id":"388325","summary":"This gene encodes a transmembrane adaptor protein that is expressed in antigen-presenting cells and is localized in the immunologic synapse. The encoded protein is involved in major histocompatibility complex class II signal transduction and immune synapse formation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]","start":5208961,"end":5234860,"strand":-1,"description":"SLP adaptor and CSK interacting membrane protein [Source:HGNC Symbol;Acc:HGNC:33504]"}, {"versioned_ensembl_gene_id":"ENSG00000262691.1","gene_symbol":"AC040160.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":67261108,"end":67263784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227660.1","gene_symbol":"UST-AS1","gene_name":"UST antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40802]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128176","summary":null,"start":148955628,"end":148964684,"strand":-1,"description":"UST antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40802]"}, {"versioned_ensembl_gene_id":"ENSG00000250138.4","gene_symbol":"AC139495.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69631963,"end":69636399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226144.2","gene_symbol":"RPS27AP3","gene_name":"ribosomal protein S27a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16538]","synonyms":"RPS27AP,bA332A4.3","biotype":"processed_pseudogene","ncbi_id":"140714","summary":null,"start":37049254,"end":37049707,"strand":1,"description":"ribosomal protein S27a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16538]"}, {"versioned_ensembl_gene_id":"ENSG00000163947.11","gene_symbol":"ARHGEF3","gene_name":"Rho guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:683]","synonyms":"XPLN,STA3,GEF3,DKFZP434F2429","biotype":"protein_coding","ncbi_id":"50650","summary":"Rho-like GTPases are involved in a variety of cellular processes, and they are activated by binding GTP and inactivated by conversion of GTP to GDP by their intrinsic GTPase activity. Guanine nucleotide exchange factors (GEFs) accelerate the GTPase activity of Rho GTPases by catalyzing their release of bound GDP. This gene encodes a guanine nucleotide exchange factor, which specifically activates two members of the Rho GTPase family: RHOA and RHOB, both of which have a role in bone cell biology. It has been identified that genetic variation in this gene plays a role in the determination of bone mineral density (BMD), indicating the implication of this gene in postmenopausal osteoporosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56727418,"end":57079329,"strand":-1,"description":"Rho guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:683]"}, {"versioned_ensembl_gene_id":"ENSG00000145626.11","gene_symbol":"UGT3A1","gene_name":"UDP glycosyltransferase family 3 member A1 [Source:HGNC Symbol;Acc:HGNC:26625]","synonyms":"FLJ34658","biotype":"protein_coding","ncbi_id":"133688","summary":null,"start":35951010,"end":36001028,"strand":-1,"description":"UDP glycosyltransferase family 3 member A1 [Source:HGNC Symbol;Acc:HGNC:26625]"}, {"versioned_ensembl_gene_id":"ENSG00000237322.1","gene_symbol":"RPL7L1P10","gene_name":"ribosomal protein L7 like 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39492]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480729","summary":null,"start":228753324,"end":228753786,"strand":1,"description":"ribosomal protein L7 like 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39492]"}, {"versioned_ensembl_gene_id":"ENSG00000232023.2","gene_symbol":"LINC01807","gene_name":"long intergenic non-protein coding RNA 1807 [Source:HGNC Symbol;Acc:HGNC:52610]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928765","summary":null,"start":228483261,"end":228611395,"strand":-1,"description":"long intergenic non-protein coding RNA 1807 [Source:HGNC Symbol;Acc:HGNC:52610]"}, {"versioned_ensembl_gene_id":"ENSG00000228226.1","gene_symbol":"AC012070.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":228683537,"end":228684580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248245.1","gene_symbol":"AC010307.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133160438,"end":133224413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250244.5","gene_symbol":"AC010307.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133256492,"end":133275977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165912.15","gene_symbol":"PACSIN3","gene_name":"protein kinase C and casein kinase substrate in neurons 3 [Source:HGNC Symbol;Acc:HGNC:8572]","synonyms":"SDPIII","biotype":"protein_coding","ncbi_id":"29763","summary":"This gene is a member of the protein kinase C and casein kinase substrate in neurons family. The encoded protein is involved in linking the actin cytoskeleton with vesicle formation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":47177525,"end":47186443,"strand":-1,"description":"protein kinase C and casein kinase substrate in neurons 3 [Source:HGNC Symbol;Acc:HGNC:8572]"}, {"versioned_ensembl_gene_id":"ENSG00000233595.2","gene_symbol":"MTND2P29","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42130]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873233","summary":null,"start":50017092,"end":50017503,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42130]"}, {"versioned_ensembl_gene_id":"ENSG00000251001.1","gene_symbol":"AC026427.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80997183,"end":80998047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258424.1","gene_symbol":"AL512791.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90402523,"end":90405235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264070.1","gene_symbol":"AC126544.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45585871,"end":45586929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279535.1","gene_symbol":"AP003476.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":118189455,"end":118189970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196074.12","gene_symbol":"SYCP2","gene_name":"synaptonemal complex protein 2 [Source:HGNC Symbol;Acc:HGNC:11490]","synonyms":"SCP2","biotype":"protein_coding","ncbi_id":"10388","summary":"The synaptonemal complex is a proteinaceous structure that links homologous chromosomes during the prophase of meiosis. The protein encoded by this gene is a major component of the synaptonemal complex and may bind DNA at scaffold attachment regions. The encoded protein requires synaptonemal complex protein 3, but not 1, for inclusion in the synaptonemal complex. [provided by RefSeq, Jul 2008]","start":59863563,"end":59933655,"strand":-1,"description":"synaptonemal complex protein 2 [Source:HGNC Symbol;Acc:HGNC:11490]"}, {"versioned_ensembl_gene_id":"ENSG00000253236.1","gene_symbol":"LINC02143","gene_name":"long intergenic non-protein coding RNA 2143 [Source:HGNC Symbol;Acc:HGNC:53003]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927835","summary":null,"start":164448422,"end":164467402,"strand":-1,"description":"long intergenic non-protein coding RNA 2143 [Source:HGNC Symbol;Acc:HGNC:53003]"}, {"versioned_ensembl_gene_id":"ENSG00000255086.1","gene_symbol":"AC024341.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26045987,"end":26047598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254754.1","gene_symbol":"AC013799.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25924188,"end":25926808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083093.9","gene_symbol":"PALB2","gene_name":"partner and localizer of BRCA2 [Source:HGNC Symbol;Acc:HGNC:26144]","synonyms":"FLJ21816,FANCN","biotype":"protein_coding","ncbi_id":"79728","summary":"This gene encodes a protein that may function in tumor suppression. This protein binds to and colocalizes with the breast cancer 2 early onset protein (BRCA2) in nuclear foci and likely permits the stable intranuclear localization and accumulation of BRCA2. [provided by RefSeq, Jul 2008]","start":23603160,"end":23641310,"strand":-1,"description":"partner and localizer of BRCA2 [Source:HGNC Symbol;Acc:HGNC:26144]"}, {"versioned_ensembl_gene_id":"ENSG00000251008.1","gene_symbol":"ORAOV1P1","gene_name":"oral cancer overexpressed 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39203]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873907","summary":null,"start":186170863,"end":186171257,"strand":-1,"description":"oral cancer overexpressed 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39203]"}, {"versioned_ensembl_gene_id":"ENSG00000162729.13","gene_symbol":"IGSF8","gene_name":"immunoglobulin superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:17813]","synonyms":"PGRL,EWI2,CD81P3,CD316","biotype":"protein_coding","ncbi_id":"93185","summary":"This gene encodes a member the EWI subfamily of the immunoglobulin protein superfamily. Members of this family contain a single transmembrane domain, an EWI (Glu-Trp-Ile)-motif and a variable number of immunoglobulin domains. This protein interacts with the tetraspanins CD81 and CD9 and may regulate their role in certain cellular functions including cell migration and viral infection. The encoded protein may also function as a tumor suppressor by inhibiting the proliferation of certain cancers. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011]","start":160091340,"end":160098943,"strand":-1,"description":"immunoglobulin superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:17813]"}, {"versioned_ensembl_gene_id":"ENSG00000180185.11","gene_symbol":"FAHD1","gene_name":"fumarylacetoacetate hydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14169]","synonyms":"DKFZP566J2046,C16orf36","biotype":"protein_coding","ncbi_id":"81889","summary":null,"start":1826941,"end":1840207,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14169]"}, {"versioned_ensembl_gene_id":"ENSG00000132911.4","gene_symbol":"NMUR2","gene_name":"neuromedin U receptor 2 [Source:HGNC Symbol;Acc:HGNC:16454]","synonyms":"NMU2R","biotype":"protein_coding","ncbi_id":"56923","summary":"This gene encodes a protein from the G-protein coupled receptor 1 family. This protein is a receptor for neuromedin U, which is a neuropeptide that is widely distributed in the gut and central nervous system. This receptor plays an important role in the regulation of food intake and body weight. [provided by RefSeq, Jul 2008]","start":152391532,"end":152433368,"strand":-1,"description":"neuromedin U receptor 2 [Source:HGNC Symbol;Acc:HGNC:16454]"}, {"versioned_ensembl_gene_id":"ENSG00000280078.1","gene_symbol":"AC016526.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76279173,"end":76283103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214301.4","gene_symbol":"AC022296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133490824,"end":133491505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244457.2","gene_symbol":"ENO1P1","gene_name":"enolase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3352]","synonyms":"ENO1P","biotype":"transcribed_processed_pseudogene","ncbi_id":"2025","summary":null,"start":236483165,"end":236484468,"strand":1,"description":"enolase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3352]"}, {"versioned_ensembl_gene_id":"ENSG00000063241.7","gene_symbol":"ISOC2","gene_name":"isochorismatase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26278]","synonyms":"FLJ23469","biotype":"protein_coding","ncbi_id":"79763","summary":null,"start":55452985,"end":55462343,"strand":-1,"description":"isochorismatase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26278]"}, {"versioned_ensembl_gene_id":"ENSG00000253538.1","gene_symbol":"AC008662.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":164209631,"end":164211892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125122.15","gene_symbol":"LRRC29","gene_name":"leucine rich repeat containing 29 [Source:HGNC Symbol;Acc:HGNC:13605]","synonyms":"FBXL9,FBL9","biotype":"protein_coding","ncbi_id":"26231","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains 9 tandem leucine-rich repeats. Two transcript variants encoding the same protein have been found for this gene. Other variants may occur, but their full-length natures have not been characterized. [provided by RefSeq, Jul 2008]","start":67207139,"end":67227048,"strand":-1,"description":"leucine rich repeat containing 29 [Source:HGNC Symbol;Acc:HGNC:13605]"}, {"versioned_ensembl_gene_id":"ENSG00000271679.1","gene_symbol":"LSM1P2","gene_name":"LSM1 homolog, mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49777]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480288","summary":null,"start":163887506,"end":163887827,"strand":-1,"description":"LSM1 homolog, mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49777]"}, {"versioned_ensembl_gene_id":"ENSG00000250366.2","gene_symbol":"TUNAR","gene_name":"TCL1 upstream neural differentiation-associated RNA [Source:HGNC Symbol;Acc:HGNC:44088]","synonyms":"TUNA,LINC00617,HI-LNC78","biotype":"protein_coding","ncbi_id":"100507043","summary":"This gene produces a spliced long non-coding RNA that may play a role in maintaining pluripotency and the neural differentiation of embryonic stem cells. Expression of this lncRNA in the caudate nucleus of brains from Huntington's Disease patients has been found to decrease as the disease progresses. It has also been suggested that this transcript may play a role in the progression of breast cancer. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2015]","start":95876392,"end":95925571,"strand":1,"description":"TCL1 upstream neural differentiation-associated RNA [Source:HGNC Symbol;Acc:HGNC:44088]"}, {"versioned_ensembl_gene_id":"ENSG00000187902.11","gene_symbol":"SHISA7","gene_name":"shisa family member 7 [Source:HGNC Symbol;Acc:HGNC:35409]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729956","summary":null,"start":55428740,"end":55442863,"strand":-1,"description":"shisa family member 7 [Source:HGNC Symbol;Acc:HGNC:35409]"}, {"versioned_ensembl_gene_id":"ENSG00000228672.3","gene_symbol":"PROB1","gene_name":"proline rich basic protein 1 [Source:HGNC Symbol;Acc:HGNC:41906]","synonyms":"C5orf65","biotype":"protein_coding","ncbi_id":"389333","summary":null,"start":139390592,"end":139395713,"strand":-1,"description":"proline rich basic protein 1 [Source:HGNC Symbol;Acc:HGNC:41906]"}, {"versioned_ensembl_gene_id":"ENSG00000169976.6","gene_symbol":"SF3B5","gene_name":"splicing factor 3b subunit 5 [Source:HGNC Symbol;Acc:HGNC:21083]","synonyms":"SF3b10,MGC3133,Ysf3","biotype":"protein_coding","ncbi_id":"83443","summary":null,"start":144094881,"end":144095573,"strand":-1,"description":"splicing factor 3b subunit 5 [Source:HGNC Symbol;Acc:HGNC:21083]"}, {"versioned_ensembl_gene_id":"ENSG00000259854.1","gene_symbol":"AP005233.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69414307,"end":69416832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249950.1","gene_symbol":"AC010587.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125862746,"end":125863193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283536.1","gene_symbol":"AC021072.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53241889,"end":53245134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260192.1","gene_symbol":"LINC02240","gene_name":"long intergenic non-protein coding RNA 2240 [Source:HGNC Symbol;Acc:HGNC:53118]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927460","summary":null,"start":125493261,"end":125602227,"strand":1,"description":"long intergenic non-protein coding RNA 2240 [Source:HGNC Symbol;Acc:HGNC:53118]"}, {"versioned_ensembl_gene_id":"ENSG00000237922.1","gene_symbol":"AL450309.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":236285976,"end":236286960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259306.2","gene_symbol":"AC020891.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51315841,"end":51321996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260266.1","gene_symbol":"AC090826.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":74350768,"end":74364620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148840.10","gene_symbol":"PPRC1","gene_name":"peroxisome proliferator-activated receptor gamma, coactivator-related 1 [Source:HGNC Symbol;Acc:HGNC:30025]","synonyms":"PRC,MGC74642,KIAA0595","biotype":"protein_coding","ncbi_id":"23082","summary":"The protein encoded by this gene is similar to PPAR-gamma coactivator 1 (PPARGC1/PGC-1), a protein that can activate mitochondrial biogenesis in part through a direct interaction with nuclear respiratory factor 1 (NRF1). This protein has been shown to interact with NRF1. It is thought to be a functional relative of PPAR-gamma coactivator 1 that activates mitochondrial biogenesis through NRF1 in response to proliferative signals. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":102132994,"end":102150331,"strand":1,"description":"peroxisome proliferator-activated receptor gamma, coactivator-related 1 [Source:HGNC Symbol;Acc:HGNC:30025]"}, {"versioned_ensembl_gene_id":"ENSG00000231700.3","gene_symbol":"AL356276.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157709086,"end":157709643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258544.1","gene_symbol":"GLRXP2","gene_name":"glutaredoxin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171418","summary":null,"start":90107675,"end":90107995,"strand":1,"description":"glutaredoxin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18376]"}, {"versioned_ensembl_gene_id":"ENSG00000132517.14","gene_symbol":"SLC52A1","gene_name":"solute carrier family 52 member 1 [Source:HGNC Symbol;Acc:HGNC:30225]","synonyms":"RFVT1,PAR2,hRFT1,GPR172B,GPCR42,FLJ10060","biotype":"protein_coding","ncbi_id":"55065","summary":"Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]","start":5032600,"end":5052009,"strand":-1,"description":"solute carrier family 52 member 1 [Source:HGNC Symbol;Acc:HGNC:30225]"}, {"versioned_ensembl_gene_id":"ENSG00000268686.1","gene_symbol":"AC010643.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49368705,"end":49388081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269842.5","gene_symbol":"AC011453.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53761961,"end":53764199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243742.5","gene_symbol":"RPLP0P2","gene_name":"ribosomal protein lateral stalk subunit P0 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17960]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"113157","summary":null,"start":61615036,"end":61639449,"strand":1,"description":"ribosomal protein lateral stalk subunit P0 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17960]"}, {"versioned_ensembl_gene_id":"ENSG00000250230.2","gene_symbol":"AP002754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61588494,"end":61607550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134873.9","gene_symbol":"CLDN10","gene_name":"claudin 10 [Source:HGNC Symbol;Acc:HGNC:2033]","synonyms":"OSP-L,CPETRL3","biotype":"protein_coding","ncbi_id":"9071","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The expression level of this gene is associated with recurrence of primary hepatocellular carcinoma. Six alternatively spliced transcript variants encoding different isoforms have been reported, but the transcript sequences of some variants are not determined.[provided by RefSeq, Jun 2010]","start":95433604,"end":95579759,"strand":1,"description":"claudin 10 [Source:HGNC Symbol;Acc:HGNC:2033]"}, {"versioned_ensembl_gene_id":"ENSG00000083123.14","gene_symbol":"BCKDHB","gene_name":"branched chain keto acid dehydrogenase E1 subunit beta [Source:HGNC Symbol;Acc:HGNC:987]","synonyms":null,"biotype":"protein_coding","ncbi_id":"594","summary":"This gene encodes the E1 beta subunit of branched-chain keto acid dehydrogenase, which is a multienzyme complex associated with the inner membrane of mitochondria. This enzyme complex functions in the catabolism of branched-chain amino acids. Mutations in this gene have been associated with maple syrup urine disease (MSUD), type 1B, a disease characterized by a maple syrup odor to the urine in addition to mental and physical retardation and feeding problems. Alternative splicing at this locus results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":80106647,"end":80346270,"strand":1,"description":"branched chain keto acid dehydrogenase E1 subunit beta [Source:HGNC Symbol;Acc:HGNC:987]"}, {"versioned_ensembl_gene_id":"ENSG00000204595.1","gene_symbol":"DPRX","gene_name":"divergent-paired related homeobox [Source:HGNC Symbol;Acc:HGNC:32166]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503834","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the DPRX homeobox gene family. Evidence of mRNA expression has not yet been found for this gene. Multiple, related processed pseudogenes have been found which are thought to reflect expression of this gene in the germ line or embryonic cells. [provided by RefSeq, Jul 2008]","start":53632056,"end":53637009,"strand":1,"description":"divergent-paired related homeobox [Source:HGNC Symbol;Acc:HGNC:32166]"}, {"versioned_ensembl_gene_id":"ENSG00000268864.4","gene_symbol":"AC011487.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53599628,"end":53608451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063587.13","gene_symbol":"ZNF275","gene_name":"zinc finger protein 275 [Source:HGNC Symbol;Acc:HGNC:13069]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10838","summary":"This gene encodes a zinc finger protein that appears to be conserved in eutheria. Its function has not yet been established. [provided by RefSeq, Jul 2010]","start":153334155,"end":153360110,"strand":1,"description":"zinc finger protein 275 [Source:HGNC Symbol;Acc:HGNC:13069]"}, {"versioned_ensembl_gene_id":"ENSG00000277376.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54799680,"end":54812030,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000235021.1","gene_symbol":"AL591848.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":246690047,"end":246691821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179240.9","gene_symbol":"AP002360.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76381313,"end":76414619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173875.13","gene_symbol":"ZNF791","gene_name":"zinc finger protein 791 [Source:HGNC Symbol;Acc:HGNC:26895]","synonyms":"FLJ90396","biotype":"protein_coding","ncbi_id":"163049","summary":null,"start":12610918,"end":12633840,"strand":1,"description":"zinc finger protein 791 [Source:HGNC Symbol;Acc:HGNC:26895]"}, {"versioned_ensembl_gene_id":"ENSG00000235533.1","gene_symbol":"AL360089.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14025971,"end":14030115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164506.14","gene_symbol":"STXBP5","gene_name":"syntaxin binding protein 5 [Source:HGNC Symbol;Acc:HGNC:19665]","synonyms":"tomosyn,LLGL3","biotype":"protein_coding","ncbi_id":"134957","summary":"Syntaxin 1 is a component of the 7S and 20S SNARE complexes which are involved in docking and fusion of synaptic vesicles with the presynaptic plasma membrane. This gene encodes a syntaxin 1 binding protein. In rat, a similar protein dissociates syntaxin 1 from the Munc18/n-Sec1/rbSec1 complex to form a 10S complex, an intermediate which can be converted to the 7S SNARE complex. Thus this protein is thought to be involved in neurotransmitter release by stimulating SNARE complex formation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":147204425,"end":147390476,"strand":1,"description":"syntaxin binding protein 5 [Source:HGNC Symbol;Acc:HGNC:19665]"}, {"versioned_ensembl_gene_id":"ENSG00000254432.1","gene_symbol":"AC113143.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60808735,"end":60809606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272397.1","gene_symbol":"AL138916.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146948528,"end":146951159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255362.1","gene_symbol":"AP000785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76210956,"end":76216025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262202.4","gene_symbol":"AC007952.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19112000,"end":19112636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260895.1","gene_symbol":"AP003071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69103493,"end":69109094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260247.1","gene_symbol":"SUB1P4","gene_name":"SUB1 homolog, transcriptional regulator pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288661","summary":null,"start":23537061,"end":23537556,"strand":1,"description":"SUB1 homolog, transcriptional regulator pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43994]"}, {"versioned_ensembl_gene_id":"ENSG00000080824.18","gene_symbol":"HSP90AA1","gene_name":"heat shock protein 90 alpha family class A member 1 [Source:HGNC Symbol;Acc:HGNC:5253]","synonyms":"HSPCA,HSPC1,HSP90N,Hsp90,Hsp89,FLJ31884","biotype":"protein_coding","ncbi_id":"3320","summary":"The protein encoded by this gene is an inducible molecular chaperone that functions as a homodimer. The encoded protein aids in the proper folding of specific target proteins by use of an ATPase activity that is modulated by co-chaperones. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":102080738,"end":102139699,"strand":-1,"description":"heat shock protein 90 alpha family class A member 1 [Source:HGNC Symbol;Acc:HGNC:5253]"}, {"versioned_ensembl_gene_id":"ENSG00000162723.9","gene_symbol":"SLAMF9","gene_name":"SLAM family member 9 [Source:HGNC Symbol;Acc:HGNC:18430]","synonyms":"SF2001,CD84-H1,CD2F-10","biotype":"protein_coding","ncbi_id":"89886","summary":"This gene encodes a member of the signaling lymphocytic activation molecule family. The encoded protein is a cell surface molecule that consists of two extracellular immunoglobulin domains, a transmembrane domain and a short cytoplasmic tail that lacks the signal transduction motifs found in other family members. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2009]","start":159951492,"end":159954254,"strand":-1,"description":"SLAM family member 9 [Source:HGNC Symbol;Acc:HGNC:18430]"}, {"versioned_ensembl_gene_id":"ENSG00000136327.6","gene_symbol":"NKX2-8","gene_name":"NK2 homeobox 8 [Source:HGNC Symbol;Acc:HGNC:16364]","synonyms":"NKX2.8,Nkx2-9,NKX2H","biotype":"protein_coding","ncbi_id":"26257","summary":"The protein encoded by this gene is a homeobox-containing developmental regulator associated with liver development. The encoded protein binds to the alpha-fetoprotein (AFP) gene promoter and increases the expression of AFP. This gene is overexpressed in some lung cancers and is linked to poor patient survival, possibly due to its resistance to cisplatin. This gene is aberrantly methylated in pancreatic cancer, deleted in squamous cell lung carcinomas, and acts as a tumor suppressor in esophageal cancer. Mutations in this gene may also be a cause of neural tube defects. [provided by RefSeq, Dec 2015]","start":36580579,"end":36582607,"strand":-1,"description":"NK2 homeobox 8 [Source:HGNC Symbol;Acc:HGNC:16364]"}, {"versioned_ensembl_gene_id":"ENSG00000251099.2","gene_symbol":"AC008967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111572236,"end":111572398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283098.1","gene_symbol":"AL132857.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":36320753,"end":36656163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258690.1","gene_symbol":"AL162464.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36788644,"end":36807163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250095.5","gene_symbol":"NREP-AS1","gene_name":"NREP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40780]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873948","summary":null,"start":111912508,"end":112017309,"strand":1,"description":"NREP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40780]"}, {"versioned_ensembl_gene_id":"ENSG00000095752.6","gene_symbol":"IL11","gene_name":"interleukin 11 [Source:HGNC Symbol;Acc:HGNC:5966]","synonyms":"IL-11,AGIF","biotype":"protein_coding","ncbi_id":"3589","summary":"The protein encoded by this gene is a member of the gp130 family of cytokines. These cytokines drive the assembly of multisubunit receptor complexes, all of which contain at least one molecule of the transmembrane signaling receptor IL6ST (gp130). This cytokine is shown to stimulate the T-cell-dependent development of immunoglobulin-producing B cells. It is also found to support the proliferation of hematopoietic stem cells and megakaryocyte progenitor cells. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":55364389,"end":55370463,"strand":-1,"description":"interleukin 11 [Source:HGNC Symbol;Acc:HGNC:5966]"}, {"versioned_ensembl_gene_id":"ENSG00000270917.1","gene_symbol":"AL161911.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120812475,"end":120812845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167641.10","gene_symbol":"PPP1R14A","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14A [Source:HGNC Symbol;Acc:HGNC:14871]","synonyms":"PPP1INL,CPI-17","biotype":"protein_coding","ncbi_id":"94274","summary":"The protein encoded by this gene belongs to the protein phosphatase 1 (PP1) inhibitor family. This protein is an inhibitor of smooth muscle myosin phosphatase, and has higher inhibitory activity when phosphorylated. Inhibition of myosin phosphatase leads to increased myosin phosphorylation and enhanced smooth muscle contraction. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Sep 2011]","start":38251237,"end":38256591,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14A [Source:HGNC Symbol;Acc:HGNC:14871]"}, {"versioned_ensembl_gene_id":"ENSG00000216753.3","gene_symbol":"HMGA1P7","gene_name":"high mobility group AT-hook 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19122]","synonyms":"HMGA1L7","biotype":"processed_pseudogene","ncbi_id":"387065","summary":null,"start":134115235,"end":134115736,"strand":-1,"description":"high mobility group AT-hook 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19122]"}, {"versioned_ensembl_gene_id":"ENSG00000136859.9","gene_symbol":"ANGPTL2","gene_name":"angiopoietin like 2 [Source:HGNC Symbol;Acc:HGNC:490]","synonyms":"HARP,ARP2","biotype":"protein_coding","ncbi_id":"23452","summary":"Angiopoietins are members of the vascular endothelial growth factor family and the only known growth factors largely specific for vascular endothelium. Angiopoietin-1, angiopoietin-2, and angiopoietin-4 participate in the formation of blood vessels. ANGPTL2 protein is a secreted glycoprotein with homology to the angiopoietins and may exert a function on endothelial cells through autocrine or paracrine action. [provided by RefSeq, Jul 2008]","start":127087332,"end":127122883,"strand":-1,"description":"angiopoietin like 2 [Source:HGNC Symbol;Acc:HGNC:490]"}, {"versioned_ensembl_gene_id":"ENSG00000254662.1","gene_symbol":"AP000781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57325603,"end":57327958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057663.14","gene_symbol":"ATG5","gene_name":"autophagy related 5 [Source:HGNC Symbol;Acc:HGNC:589]","synonyms":"APG5L,APG5,hAPG5,ASP","biotype":"protein_coding","ncbi_id":"9474","summary":"The protein encoded by this gene, in combination with autophagy protein 12, functions as an E1-like activating enzyme in a ubiquitin-like conjugating system. The encoded protein is involved in several cellular processes, including autophagic vesicle formation, mitochondrial quality control after oxidative damage, negative regulation of the innate antiviral immune response, lymphocyte development and proliferation, MHC II antigen presentation, adipocyte differentiation, and apoptosis. Several transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":106045423,"end":106325791,"strand":-1,"description":"autophagy related 5 [Source:HGNC Symbol;Acc:HGNC:589]"}, {"versioned_ensembl_gene_id":"ENSG00000153208.16","gene_symbol":"MERTK","gene_name":"MER proto-oncogene, tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7027]","synonyms":"Tyro12,RP38,mer,c-Eyk","biotype":"protein_coding","ncbi_id":"10461","summary":"This gene is a member of the MER/AXL/TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type-III domains, two Ig-like C2-type (immunoglobulin-like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP). [provided by RefSeq, Jul 2008]","start":111898479,"end":112029561,"strand":1,"description":"MER proto-oncogene, tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:7027]"}, {"versioned_ensembl_gene_id":"ENSG00000135917.13","gene_symbol":"SLC19A3","gene_name":"solute carrier family 19 member 3 [Source:HGNC Symbol;Acc:HGNC:16266]","synonyms":"THTR2","biotype":"protein_coding","ncbi_id":"80704","summary":"This gene encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Mutations in this gene cause biotin-responsive basal ganglia disease (BBGD); a recessive disorder manifested in childhood that progresses to chronic encephalopathy, dystonia, quadriparesis, and death if untreated. Patients with BBGD have bilateral necrosis in the head of the caudate nucleus and in the putamen. Administration of high doses of biotin in the early progression of the disorder eliminates pathological symptoms while delayed treatment results in residual paraparesis, mild cognitive disability, or dystonia. Administration of thiamine is ineffective in the treatment of this disorder. Experiments have failed to show that this protein can transport biotin. Mutations in this gene also cause a Wernicke's-like encephalopathy.[provided by RefSeq, Jan 2010]","start":227685210,"end":227718012,"strand":-1,"description":"solute carrier family 19 member 3 [Source:HGNC Symbol;Acc:HGNC:16266]"}, {"versioned_ensembl_gene_id":"ENSG00000275160.1","gene_symbol":"AL354718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41479960,"end":41480548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198125.12","gene_symbol":"MB","gene_name":"myoglobin [Source:HGNC Symbol;Acc:HGNC:6915]","synonyms":"PVALB","biotype":"protein_coding","ncbi_id":"4151","summary":"This gene encodes a member of the globin superfamily and is predominantly expressed in skeletal and cardiac muscles. The encoded protein forms a monomeric globular haemoprotein that is primarily responsible for the storage and facilitated transfer of oxygen from the cell membrane to the mitochondria. This protein also plays a role in regulating physiological levels of nitric oxide. Multiple transcript variants encoding distinct isoforms exist for this gene. [provided by RefSeq, May 2020]","start":35606764,"end":35637951,"strand":-1,"description":"myoglobin [Source:HGNC Symbol;Acc:HGNC:6915]"}, {"versioned_ensembl_gene_id":"ENSG00000146216.11","gene_symbol":"TTBK1","gene_name":"tau tubulin kinase 1 [Source:HGNC Symbol;Acc:HGNC:19140]","synonyms":"KIAA1855","biotype":"protein_coding","ncbi_id":"84630","summary":"Summary:This gene belongs to the casein kinase 1 superfamily. The encoded protein is a neuron-specific, serine/threonine and tyrosine kinase, which regulates phosphorylation of tau, a protein that associates with microtubule assemblies and stabilizes them. Genetic variants in this gene are associated with Alzheimer's disease. [provided by RefSeq, Jul 2016]","start":43243680,"end":43288259,"strand":1,"description":"tau tubulin kinase 1 [Source:HGNC Symbol;Acc:HGNC:19140]"}, {"versioned_ensembl_gene_id":"ENSG00000275450.1","gene_symbol":"PTGER4P2-CDK2AP2P2","gene_name":"PTGER4P2-CDK2AP2P2 readthrough, transcribed pseudogene [Source:NCBI gene;Acc:442421]","synonyms":null,"biotype":"lincRNA","ncbi_id":"442421","summary":"This locus represents naturally-occurring readthrough transcription between two pseudogenes, PTGER4P2 (prostaglandin E receptor 4 pseudogene 2) and CDK2AP2P2 (cyclin-dependent kinase 2 associated protein 2 pseudogene 2). The individual pseudogene loci are not curated as transcribed regions. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Jan 2016]","start":41276280,"end":41282846,"strand":1,"description":"PTGER4P2-CDK2AP2P2 readthrough, transcribed pseudogene [Source:NCBI gene;Acc:442421]"}, {"versioned_ensembl_gene_id":"ENSG00000274680.1","gene_symbol":"MYO5BP1","gene_name":"myosin VB pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38495]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441420","summary":null,"start":41292887,"end":41294125,"strand":1,"description":"myosin VB pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38495]"}, {"versioned_ensembl_gene_id":"ENSG00000112667.12","gene_symbol":"DNPH1","gene_name":"2'-deoxynucleoside 5'-phosphate N-hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:21218]","synonyms":"rcl,dJ330M21.3,C6orf108","biotype":"protein_coding","ncbi_id":"10591","summary":"This gene was identified on the basis of its stimulation by c-Myc protein. The latter is a transcription factor that participates in the regulation of cell proliferation, differentiation, and apoptosis. The exact function of this gene is not known but studies in rat suggest a role in cellular proliferation and c-Myc-mediated transformation. Two alternative transcripts encoding different proteins have been described. [provided by RefSeq, Jul 2008]","start":43225629,"end":43229484,"strand":-1,"description":"2'-deoxynucleoside 5'-phosphate N-hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:21218]"}, {"versioned_ensembl_gene_id":"ENSG00000081014.10","gene_symbol":"AP4E1","gene_name":"adaptor related protein complex 4 epsilon 1 subunit [Source:HGNC Symbol;Acc:HGNC:573]","synonyms":"SPG51,AP-4-EPSILON","biotype":"protein_coding","ncbi_id":"23431","summary":"This gene encodes a member of the adaptor complexes large subunit protein family. These proteins are components of the heterotetrameric adaptor protein complexes, which play important roles in the secretory and endocytic pathways by mediating vesicle formation and sorting of integral membrane proteins. The encoded protein is a large subunit of adaptor protein complex-4, which is associated with both clathrin- and nonclathrin-coated vesicles. Disruption of this gene may be associated with cerebral palsy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":50908672,"end":51005900,"strand":1,"description":"adaptor related protein complex 4 epsilon 1 subunit [Source:HGNC Symbol;Acc:HGNC:573]"}, {"versioned_ensembl_gene_id":"ENSG00000278909.1","gene_symbol":"AC007608.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50555355,"end":50558719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205414.1","gene_symbol":"AC007608.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50606076,"end":50613684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248951.2","gene_symbol":"MTCO2P32","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52161]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075196","summary":null,"start":1370543,"end":1370945,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52161]"}, {"versioned_ensembl_gene_id":"ENSG00000235286.1","gene_symbol":"AP000925.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111670956,"end":111672404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267151.5","gene_symbol":"MIR2117HG","gene_name":"MIR2117 host gene [Source:HGNC Symbol;Acc:HGNC:51999]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106660605","summary":null,"start":43444707,"end":43451200,"strand":1,"description":"MIR2117 host gene [Source:HGNC Symbol;Acc:HGNC:51999]"}, {"versioned_ensembl_gene_id":"ENSG00000233049.6","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DDX16,PRPF2,DBP2,Prp2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30697750,"end":30717697,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000174109.4","gene_symbol":"C16orf91","gene_name":"chromosome 16 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:27558]","synonyms":"URLC5,gs103,CCSMST1","biotype":"protein_coding","ncbi_id":"283951","summary":null,"start":1419744,"end":1420800,"strand":-1,"description":"chromosome 16 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:27558]"}, {"versioned_ensembl_gene_id":"ENSG00000268355.1","gene_symbol":"AC243960.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41531206,"end":41532174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105967.15","gene_symbol":"TFEC","gene_name":"transcription factor EC [Source:HGNC Symbol;Acc:HGNC:11754]","synonyms":"TFECL,TCFEC,bHLHe34","biotype":"protein_coding","ncbi_id":"22797","summary":"This gene encodes a member of the micropthalmia (MiT) family of basic helix-loop-helix leucine zipper transcription factors. MiT transcription factors regulate the expression of target genes by binding to E-box recognition sequences as homo- or heterodimers, and play roles in multiple cellular processes including survival, growth and differentiation. The encoded protein is a transcriptional activator of the nonmuscle myosin II heavy chain-A gene, and may also co-regulate target genes in osteoclasts as a heterodimer with micropthalmia-associated transcription factor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":115935148,"end":116159896,"strand":-1,"description":"transcription factor EC [Source:HGNC Symbol;Acc:HGNC:11754]"}, {"versioned_ensembl_gene_id":"ENSG00000261499.2","gene_symbol":"AC233699.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36274191,"end":36320547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227593.2","gene_symbol":"PHBP16","gene_name":"prohibitin pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51549]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128102","summary":null,"start":94055023,"end":94055972,"strand":-1,"description":"prohibitin pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51549]"}, {"versioned_ensembl_gene_id":"ENSG00000197323.11","gene_symbol":"TRIM33","gene_name":"tripartite motif containing 33 [Source:HGNC Symbol;Acc:HGNC:16290]","synonyms":"TIF1GAMMA,TIF1G,TF1G,RFG7,PTC7,KIAA1113,FLJ11429,TIFGAMMA","biotype":"protein_coding","ncbi_id":"51592","summary":"The protein encoded by this gene is thought to be a transcriptional corepressor. However, molecules that interact with this protein have not yet been identified. The protein is a member of the tripartite motif family. This motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Three alternatively spliced transcript variants for this gene have been described, however, the full-length nature of one variant has not been determined. [provided by RefSeq, Jul 2008]","start":114392777,"end":114511160,"strand":-1,"description":"tripartite motif containing 33 [Source:HGNC Symbol;Acc:HGNC:16290]"}, {"versioned_ensembl_gene_id":"ENSG00000108947.4","gene_symbol":"EFNB3","gene_name":"ephrin B3 [Source:HGNC Symbol;Acc:HGNC:3228]","synonyms":"LERK-8,EPLG8","biotype":"protein_coding","ncbi_id":"1949","summary":" EFNB3, a member of the ephrin gene family, is important in brain development as well as in its maintenance. Moreover, since levels of EFNB3 expression were particularly high in several forebrain subregions compared to other brain subregions, it may play a pivotal role in forebrain function. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. EPH Receptors typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin ligands and receptors have been named by the Eph Nomenclature Committee (1997). Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are similarly divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. [provided by RefSeq, Jul 2008]","start":7705202,"end":7711378,"strand":1,"description":"ephrin B3 [Source:HGNC Symbol;Acc:HGNC:3228]"}, {"versioned_ensembl_gene_id":"ENSG00000141696.12","gene_symbol":"P3H4","gene_name":"prolyl 3-hydroxylase family member 4 (non-enzymatic) [Source:HGNC Symbol;Acc:HGNC:16946]","synonyms":"NO55,LEPREL4,SC65","biotype":"protein_coding","ncbi_id":"10609","summary":"This nucleolar protein was first characterized because it was an autoantigen in cases on interstitial cystitis. The protein, with a predicted molecular weight of 50 kDa, appears to be localized in the particulate compartment of the interphase nucleolus, with a distribution distinct from that of nucleolar protein B23. During mitosis it is associated with chromosomes. [provided by RefSeq, Jul 2008]","start":41801947,"end":41812604,"strand":-1,"description":"prolyl 3-hydroxylase family member 4 (non-enzymatic) [Source:HGNC Symbol;Acc:HGNC:16946]"}, {"versioned_ensembl_gene_id":"ENSG00000254826.1","gene_symbol":"AP001922.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75775904,"end":75776929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184988.8","gene_symbol":"TMEM106A","gene_name":"transmembrane protein 106A [Source:HGNC Symbol;Acc:HGNC:28288]","synonyms":"MGC20235","biotype":"protein_coding","ncbi_id":"113277","summary":null,"start":43211835,"end":43220041,"strand":1,"description":"transmembrane protein 106A [Source:HGNC Symbol;Acc:HGNC:28288]"}, {"versioned_ensembl_gene_id":"ENSG00000233721.1","gene_symbol":"AL356309.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126516417,"end":126518808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222047.8","gene_symbol":"C10orf55","gene_name":"chromosome 10 open reading frame 55 [Source:HGNC Symbol;Acc:HGNC:31008]","synonyms":"bA417O11.3","biotype":"protein_coding","ncbi_id":"414236","summary":null,"start":73909969,"end":73922777,"strand":-1,"description":"chromosome 10 open reading frame 55 [Source:HGNC Symbol;Acc:HGNC:31008]"}, {"versioned_ensembl_gene_id":"ENSG00000005001.9","gene_symbol":"PRSS22","gene_name":"protease, serine 22 [Source:HGNC Symbol;Acc:HGNC:14368]","synonyms":"BSSP-4,SP001LA,hBSSP-4,BSSP-4,SP001LA,hBSSP-4","biotype":"protein_coding","ncbi_id":"64063","summary":"This gene encodes a member of the trypsin family of serine proteases. The enzyme is expressed in the airways in a developmentally regulated manner. The gene is part of a cluster of serine protease genes on chromosome 16. [provided by RefSeq, Jul 2008]","start":2852727,"end":2858170,"strand":-1,"description":"protease, serine 22 [Source:HGNC Symbol;Acc:HGNC:14368]"}, {"versioned_ensembl_gene_id":"ENSG00000189127.7","gene_symbol":"ANKRD34B","gene_name":"ankyrin repeat domain 34B [Source:HGNC Symbol;Acc:HGNC:33736]","synonyms":"DP58","biotype":"protein_coding","ncbi_id":"340120","summary":null,"start":80556755,"end":80570488,"strand":-1,"description":"ankyrin repeat domain 34B [Source:HGNC Symbol;Acc:HGNC:33736]"}, {"versioned_ensembl_gene_id":"ENSG00000271780.1","gene_symbol":"AL118558.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101948347,"end":101949425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227345.8","gene_symbol":"PARG","gene_name":"poly(ADP-ribose) glycohydrolase [Source:HGNC Symbol;Acc:HGNC:8605]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8505","summary":"Poly(ADP-ribose) glycohydrolase (PARG) is the major enzyme responsible for the catabolism of poly(ADP-ribose), a reversible covalent-modifier of chromosomal proteins. The protein is found in many tissues and may be subject to proteolysis generating smaller, active products. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":49818279,"end":49970203,"strand":-1,"description":"poly(ADP-ribose) glycohydrolase [Source:HGNC Symbol;Acc:HGNC:8605]"}, {"versioned_ensembl_gene_id":"ENSG00000205056.8","gene_symbol":"LINC02397","gene_name":"long intergenic non-protein coding RNA 2397 [Source:HGNC Symbol;Acc:HGNC:53323]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507616","summary":null,"start":92466451,"end":92492091,"strand":1,"description":"long intergenic non-protein coding RNA 2397 [Source:HGNC Symbol;Acc:HGNC:53323]"}, {"versioned_ensembl_gene_id":"ENSG00000070061.14","gene_symbol":"ELP1","gene_name":"elongator complex protein 1 [Source:HGNC Symbol;Acc:HGNC:5959]","synonyms":"TOT1,IKI3,IKBKAP,IKAP,DYS","biotype":"protein_coding","ncbi_id":"8518","summary":"The protein encoded by this gene is a scaffold protein and a regulator for three different kinases involved in proinflammatory signaling. The encoded protein can bind NF-kappa-B-inducing kinase and I-kappa-B kinases through separate domains and assemble them into an active kinase complex. Mutations in this gene have been associated with familial dysautonomia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":108867517,"end":108934116,"strand":-1,"description":"elongator complex protein 1 [Source:HGNC Symbol;Acc:HGNC:5959]"}, {"versioned_ensembl_gene_id":"ENSG00000267288.2","gene_symbol":"AC138150.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45168800,"end":45171584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133639.4","gene_symbol":"BTG1","gene_name":"BTG anti-proliferation factor 1 [Source:HGNC Symbol;Acc:HGNC:1130]","synonyms":"APRO2","biotype":"protein_coding","ncbi_id":"694","summary":"This gene is a member of an anti-proliferative gene family that regulates cell growth and differentiation. Expression of this gene is highest in the G0/G1 phases of the cell cycle and downregulated when cells progressed through G1. The encoded protein interacts with several nuclear receptors, and functions as a coactivator of cell differentiation. This locus has been shown to be involved in a t(8;12)(q24;q22) chromosomal translocation in a case of B-cell chronic lymphocytic leukemia. [provided by RefSeq, Oct 2008]","start":92140278,"end":92145897,"strand":-1,"description":"BTG anti-proliferation factor 1 [Source:HGNC Symbol;Acc:HGNC:1130]"}, {"versioned_ensembl_gene_id":"ENSG00000076924.11","gene_symbol":"XAB2","gene_name":"XPA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14089]","synonyms":"SYF1,NTC90,HCRN,HCNP","biotype":"protein_coding","ncbi_id":"56949","summary":null,"start":7619525,"end":7629565,"strand":-1,"description":"XPA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14089]"}, {"versioned_ensembl_gene_id":"ENSG00000233095.8","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29824463,"end":29828635,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000264066.6","gene_symbol":"AC024267.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28861072,"end":28861966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257242.7","gene_symbol":"LINC01619","gene_name":"long intergenic non-protein coding RNA 1619 [Source:HGNC Symbol;Acc:HGNC:27409]","synonyms":"C12orf79","biotype":"processed_transcript","ncbi_id":"256021","summary":null,"start":91984976,"end":92142914,"strand":-1,"description":"long intergenic non-protein coding RNA 1619 [Source:HGNC Symbol;Acc:HGNC:27409]"}, {"versioned_ensembl_gene_id":"ENSG00000182557.7","gene_symbol":"SPNS3","gene_name":"sphingolipid transporter 3 (putative) [Source:HGNC Symbol;Acc:HGNC:28433]","synonyms":"MGC29671","biotype":"protein_coding","ncbi_id":"201305","summary":null,"start":4433688,"end":4488208,"strand":1,"description":"sphingolipid transporter 3 (putative) [Source:HGNC Symbol;Acc:HGNC:28433]"}, {"versioned_ensembl_gene_id":"ENSG00000258699.1","gene_symbol":"AL357093.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89355060,"end":89356571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241829.1","gene_symbol":"AC026801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34883057,"end":34883520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211930.1","gene_symbol":"IGHD3-3","gene_name":"immunoglobulin heavy diversity 3-3 [Source:HGNC Symbol;Acc:HGNC:5498]","synonyms":"IGHD33,DXP4","biotype":"IG_D_gene","ncbi_id":"28501","summary":"IGHD3-3 belongs to a cluster of approximately 25 functional diversity (D) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the D gene cluster, see (MIM 146910).[supplied by OMIM, Apr 2008]","start":105914359,"end":105914389,"strand":-1,"description":"immunoglobulin heavy diversity 3-3 [Source:HGNC Symbol;Acc:HGNC:5498]"}, {"versioned_ensembl_gene_id":"ENSG00000237360.2","gene_symbol":"CHCHD4P2","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44490]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128657","summary":null,"start":108097432,"end":108097851,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44490]"}, {"versioned_ensembl_gene_id":"ENSG00000224045.1","gene_symbol":"AL354761.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135588002,"end":135591975,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211924.1","gene_symbol":"IGHD3-9","gene_name":"immunoglobulin heavy diversity 3-9 [Source:HGNC Symbol;Acc:HGNC:5499]","synonyms":"IGHD39,DXP1","biotype":"IG_D_gene","ncbi_id":"28500","summary":null,"start":105904681,"end":105904711,"strand":-1,"description":"immunoglobulin heavy diversity 3-9 [Source:HGNC Symbol;Acc:HGNC:5499]"}, {"versioned_ensembl_gene_id":"ENSG00000076826.9","gene_symbol":"CAMSAP3","gene_name":"calmodulin regulated spectrin associated protein family member 3 [Source:HGNC Symbol;Acc:HGNC:29307]","synonyms":"PPP1R80,Nezha,KIAA1543","biotype":"protein_coding","ncbi_id":"57662","summary":null,"start":7595902,"end":7618304,"strand":1,"description":"calmodulin regulated spectrin associated protein family member 3 [Source:HGNC Symbol;Acc:HGNC:29307]"}, {"versioned_ensembl_gene_id":"ENSG00000271099.1","gene_symbol":"AL357315.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104860449,"end":104862123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211912.1","gene_symbol":"IGHD2-21","gene_name":"immunoglobulin heavy diversity 2-21 [Source:HGNC Symbol;Acc:HGNC:5491]","synonyms":"IGHD221","biotype":"IG_D_gene","ncbi_id":"28502","summary":null,"start":105888551,"end":105888578,"strand":-1,"description":"immunoglobulin heavy diversity 2-21 [Source:HGNC Symbol;Acc:HGNC:5491]"}, {"versioned_ensembl_gene_id":"ENSG00000102854.15","gene_symbol":"MSLN","gene_name":"mesothelin [Source:HGNC Symbol;Acc:HGNC:7371]","synonyms":"MPF,CAK1","biotype":"protein_coding","ncbi_id":"10232","summary":"This gene encodes a preproprotein that is proteolytically processed to generate two protein products, megakaryocyte potentiating factor and mesothelin. Megakaryocyte potentiating factor functions as a cytokine that can stimulate colony formation of bone marrow megakaryocytes. Mesothelin is a glycosylphosphatidylinositol-anchored cell-surface protein that may function as a cell adhesion protein. This protein is overexpressed in epithelial mesotheliomas, ovarian cancers and in specific squamous cell carcinomas. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":760762,"end":768865,"strand":1,"description":"mesothelin [Source:HGNC Symbol;Acc:HGNC:7371]"}, {"versioned_ensembl_gene_id":"ENSG00000129965.14","gene_symbol":"INS-IGF2","gene_name":"INS-IGF2 readthrough [Source:HGNC Symbol;Acc:HGNC:33527]","synonyms":null,"biotype":"protein_coding","ncbi_id":"723961","summary":"This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5' region and to the IGF2 gene in the 3' region. One transcript is predicted to encode a protein which shares the N-terminus with the INS protein but has a distinct and longer C-terminus, whereas the other transcript is a candidate for nonsense-mediated decay (NMD). The transcripts are imprinted and are paternally expressed in the limb and eye. [provided by RefSeq, Jul 2008]","start":2131395,"end":2161209,"strand":-1,"description":"INS-IGF2 readthrough [Source:HGNC Symbol;Acc:HGNC:33527]"}, {"versioned_ensembl_gene_id":"ENSG00000145391.13","gene_symbol":"SETD7","gene_name":"SET domain containing lysine methyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:30412]","synonyms":"Set9,SET7/9,SET7,KMT7,KIAA1717","biotype":"protein_coding","ncbi_id":"80854","summary":null,"start":139495941,"end":139606699,"strand":-1,"description":"SET domain containing lysine methyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:30412]"}, {"versioned_ensembl_gene_id":"ENSG00000273175.1","gene_symbol":"BX323046.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":244864738,"end":244865272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211899.9","gene_symbol":"IGHM","gene_name":"immunoglobulin heavy constant mu [Source:HGNC Symbol;Acc:HGNC:5541]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3507","summary":"Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains and 2 identical light chains (see MIM 147200) joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. Each Ig heavy chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by an individual C region gene, that determines the isotype of the antibody and provides effector or signaling functions. The heavy chain V region is encoded by 1 each of 3 types of genes: V genes (see MIM 147070), joining (J) genes (see MIM 147010), and diversity (D) genes (see MIM 146910). The C region genes are clustered downstream of the V region genes within the heavy chain locus on chromosome 14. The IGHM gene encodes the C region of the mu heavy chain, which defines the IgM isotype. Naive B cells express the transmembrane forms of IgM and IgD (see IGHD; MIM 1471770) on their surface. During an antibody response, activated B cells can switch to the expression of individual downstream heavy chain C region genes by a process of somatic recombination known as isotype switching. In addition, secreted Ig forms that act as antibodies can be produced by alternative RNA processing of the heavy chain C region sequences. Although the membrane forms of all Ig isotypes are monomeric, secreted IgM forms pentamers, and occasionally hexamers, in plasma (summary by Janeway et al., 2005).[supplied by OMIM, Aug 2010]","start":105851708,"end":105856218,"strand":-1,"description":"immunoglobulin heavy constant mu [Source:HGNC Symbol;Acc:HGNC:5541]"}, {"versioned_ensembl_gene_id":"ENSG00000228126.1","gene_symbol":"FALEC","gene_name":"focally amplified long non-coding RNA in epithelial cancer [Source:HGNC Symbol;Acc:HGNC:43713]","synonyms":"ncRNA-a1,LINC00568,FAL1","biotype":"lincRNA","ncbi_id":"100874054","summary":null,"start":150515757,"end":150518032,"strand":1,"description":"focally amplified long non-coding RNA in epithelial cancer [Source:HGNC Symbol;Acc:HGNC:43713]"}, {"versioned_ensembl_gene_id":"ENSG00000226663.2","gene_symbol":"MTND4P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42225]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873256","summary":null,"start":235540053,"end":235541415,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42225]"}, {"versioned_ensembl_gene_id":"ENSG00000225184.1","gene_symbol":"AL929561.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29124201,"end":29128899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238236.1","gene_symbol":"MTCYBP14","gene_name":"mitochondrially encoded cytochrome b pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075120","summary":null,"start":235519971,"end":235520685,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51960]"}, {"versioned_ensembl_gene_id":"ENSG00000224721.1","gene_symbol":"AC007182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75574888,"end":75579588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279905.1","gene_symbol":"AC063926.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130425004,"end":130430661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279146.1","gene_symbol":"AC063926.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130465008,"end":130466315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258204.1","gene_symbol":"AC008126.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98794485,"end":98794964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238176.1","gene_symbol":"AL390061.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36940109,"end":36943932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000015479.18","gene_symbol":"MATR3","gene_name":"matrin 3 [Source:HGNC Symbol;Acc:HGNC:6912]","synonyms":"VCPDM,VCPDM,MPD2,MPD2,MGC9105,ALS21,KIAA0723","biotype":"protein_coding","ncbi_id":"9782","summary":"This gene encodes a nuclear matrix protein, which is proposed to stabilize certain messenger RNA species. Mutations of this gene are associated with distal myopathy 2, which often includes vocal cord and pharyngeal weakness. Alternatively spliced transcript variants, including read-through transcripts composed of the upstream small nucleolar RNA host gene 4 (non-protein coding) and matrin 3 gene sequence, have been identified. Pseudogenes of this gene are located on chromosomes 1 and X. [provided by RefSeq, Aug 2013]","start":139293648,"end":139331677,"strand":1,"description":"matrin 3 [Source:HGNC Symbol;Acc:HGNC:6912]"}, {"versioned_ensembl_gene_id":"ENSG00000266013.1","gene_symbol":"LINC02079","gene_name":"long intergenic non-protein coding RNA 2079 [Source:HGNC Symbol;Acc:HGNC:52927]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371766","summary":null,"start":39026715,"end":39027110,"strand":-1,"description":"long intergenic non-protein coding RNA 2079 [Source:HGNC Symbol;Acc:HGNC:52927]"}, {"versioned_ensembl_gene_id":"ENSG00000273738.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874290,"end":54891462,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000223901.2","gene_symbol":"AP001469.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46220269,"end":46225364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260537.2","gene_symbol":"AC012184.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":70299194,"end":70372582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211893.4","gene_symbol":"IGHG2","gene_name":"immunoglobulin heavy constant gamma 2 (G2m marker) [Source:HGNC Symbol;Acc:HGNC:5526]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3501","summary":null,"start":105639559,"end":105644790,"strand":-1,"description":"immunoglobulin heavy constant gamma 2 (G2m marker) [Source:HGNC Symbol;Acc:HGNC:5526]"}, {"versioned_ensembl_gene_id":"ENSG00000258876.1","gene_symbol":"TGFB3-AS1","gene_name":"TGFB3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53144]","synonyms":"ENST00000553732","biotype":"lincRNA","ncbi_id":"109729179","summary":null,"start":75970924,"end":75971587,"strand":1,"description":"TGFB3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53144]"}, {"versioned_ensembl_gene_id":"ENSG00000133935.6","gene_symbol":"ERG28","gene_name":"ergosterol biosynthesis 28 homolog [Source:HGNC Symbol;Acc:HGNC:1187]","synonyms":"NET51,C14orf1","biotype":"protein_coding","ncbi_id":"11161","summary":null,"start":75649791,"end":75661189,"strand":-1,"description":"ergosterol biosynthesis 28 homolog [Source:HGNC Symbol;Acc:HGNC:1187]"}, {"versioned_ensembl_gene_id":"ENSG00000136448.11","gene_symbol":"NMT1","gene_name":"N-myristoyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:7857]","synonyms":"NMT","biotype":"protein_coding","ncbi_id":"4836","summary":"Myristate, a rare 14-carbon saturated fatty acid, is cotranslationally attached by an amide linkage to the N-terminal glycine residue of cellular and viral proteins with diverse functions. N-myristoyltransferase (NMT; EC 2.3.1.97) catalyzes the transfer of myristate from CoA to proteins. N-myristoylation appears to be irreversible and is required for full expression of the biologic activities of several N-myristoylated proteins, including the alpha subunit of the signal-transducing guanine nucleotide-binding protein (G protein) GO (GNAO1; MIM 139311) (Duronio et al., 1992 [PubMed 1570339]).[supplied by OMIM, Nov 2008]","start":45051610,"end":45109016,"strand":1,"description":"N-myristoyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:7857]"}, {"versioned_ensembl_gene_id":"ENSG00000267809.1","gene_symbol":"NDUFV2P1","gene_name":"NADH:ubiquinone oxidoreductase core subunit V2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"4730","summary":null,"start":53223973,"end":53224879,"strand":-1,"description":"NADH:ubiquinone oxidoreductase core subunit V2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7718]"}, {"versioned_ensembl_gene_id":"ENSG00000254943.1","gene_symbol":"AP003501.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124891304,"end":124892126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132010.15","gene_symbol":"ZNF20","gene_name":"zinc finger protein 20 [Source:HGNC Symbol;Acc:HGNC:12992]","synonyms":"KOX13","biotype":"protein_coding","ncbi_id":"7568","summary":null,"start":12092843,"end":12140407,"strand":-1,"description":"zinc finger protein 20 [Source:HGNC Symbol;Acc:HGNC:12992]"}, {"versioned_ensembl_gene_id":"ENSG00000064652.10","gene_symbol":"SNX24","gene_name":"sorting nexin 24 [Source:HGNC Symbol;Acc:HGNC:21533]","synonyms":"SBBI31","biotype":"protein_coding","ncbi_id":"28966","summary":null,"start":122843439,"end":123029354,"strand":1,"description":"sorting nexin 24 [Source:HGNC Symbol;Acc:HGNC:21533]"}, {"versioned_ensembl_gene_id":"ENSG00000234402.1","gene_symbol":"ELK2BP","gene_name":"ELK2B, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3324]","synonyms":"ELK2P2,ELK2.2","biotype":"unprocessed_pseudogene","ncbi_id":"9995","summary":null,"start":105546610,"end":105549694,"strand":-1,"description":"ELK2B, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3324]"}, {"versioned_ensembl_gene_id":"ENSG00000269706.1","gene_symbol":"AC008687.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49050217,"end":49050846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229534.1","gene_symbol":"HNRNPA1P53","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:48783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728732","summary":null,"start":5571247,"end":5572192,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:48783]"}, {"versioned_ensembl_gene_id":"ENSG00000235658.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30671478,"end":30691459,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000267685.2","gene_symbol":"NTF6B","gene_name":"neurotrophin 6 beta (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8026]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"4911","summary":null,"start":49038479,"end":49039038,"strand":-1,"description":"neurotrophin 6 beta (pseudogene) [Source:HGNC Symbol;Acc:HGNC:8026]"}, {"versioned_ensembl_gene_id":"ENSG00000188747.8","gene_symbol":"NOXA1","gene_name":"NADPH oxidase activator 1 [Source:HGNC Symbol;Acc:HGNC:10668]","synonyms":"NY-CO-31,FLJ25475,SDCCAG31","biotype":"protein_coding","ncbi_id":"10811","summary":"This gene encodes a protein which activates NADPH oxidases, enzymes which catalyze a reaction generating reactive oxygen species. The encoded protein contains four N-terminal tetratricopeptide domains and a C-terminal Src homology 3 domain. Interaction between the encoded protein and proteins in the oxidase regulatory complex occur via the tetratricopeptide domains. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":137423350,"end":137434406,"strand":1,"description":"NADPH oxidase activator 1 [Source:HGNC Symbol;Acc:HGNC:10668]"}, {"versioned_ensembl_gene_id":"ENSG00000223403.3","gene_symbol":"MEG9","gene_name":"maternally expressed 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43874]","synonyms":"LINC00584","biotype":"lincRNA","ncbi_id":"100507257","summary":null,"start":101069911,"end":101072937,"strand":1,"description":"maternally expressed 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43874]"}, {"versioned_ensembl_gene_id":"ENSG00000278729.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54654506,"end":54666521,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000197585.9","gene_symbol":"AC068051.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":214250040,"end":214684246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266048.1","gene_symbol":"AC091178.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39033926,"end":39034042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255460.1","gene_symbol":"ZDHHC20P3","gene_name":"zinc finger DHHC-type containing 20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874348","summary":null,"start":75228322,"end":75228657,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39775]"}, {"versioned_ensembl_gene_id":"ENSG00000130032.15","gene_symbol":"PRRG3","gene_name":"proline rich and Gla domain 3 [Source:HGNC Symbol;Acc:HGNC:30798]","synonyms":"TMG3","biotype":"protein_coding","ncbi_id":"79057","summary":"This gene encodes a protein which contains a vitamin K-dependent carboxylation/gamma-carboxyglutamic domain. The encoded protein is a member of a family of vitamin K-dependent transmembrane proteins which contain a glutamate-rich extracellular domain. [provided by RefSeq, Aug 2011]","start":151695124,"end":151705924,"strand":1,"description":"proline rich and Gla domain 3 [Source:HGNC Symbol;Acc:HGNC:30798]"}, {"versioned_ensembl_gene_id":"ENSG00000265428.1","gene_symbol":"AC006441.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38996323,"end":38996624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130731.15","gene_symbol":"METTL26","gene_name":"methyltransferase like 26 [Source:HGNC Symbol;Acc:HGNC:14141]","synonyms":"MGC13114,C16orf13","biotype":"protein_coding","ncbi_id":"84326","summary":null,"start":634427,"end":636366,"strand":-1,"description":"methyltransferase like 26 [Source:HGNC Symbol;Acc:HGNC:14141]"}, {"versioned_ensembl_gene_id":"ENSG00000225037.1","gene_symbol":"EIF1AX-AS1","gene_name":"EIF1AX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40208]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874078","summary":null,"start":20139968,"end":20140444,"strand":1,"description":"EIF1AX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40208]"}, {"versioned_ensembl_gene_id":"ENSG00000274349.4","gene_symbol":"ZNF658","gene_name":"zinc finger protein 658 [Source:HGNC Symbol;Acc:HGNC:25226]","synonyms":"MGC35232,FLJ32813,DKFZp572C163","biotype":"protein_coding","ncbi_id":"26149","summary":null,"start":66856426,"end":66932141,"strand":1,"description":"zinc finger protein 658 [Source:HGNC Symbol;Acc:HGNC:25226]"}, {"versioned_ensembl_gene_id":"ENSG00000250092.2","gene_symbol":"AC096576.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21582096,"end":21613728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259066.5","gene_symbol":"AL110118.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":93184973,"end":93218586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237793.3","gene_symbol":"RPL18AP16","gene_name":"ribosomal protein L18a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36288]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347544","summary":null,"start":153662162,"end":153662692,"strand":1,"description":"ribosomal protein L18a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36288]"}, {"versioned_ensembl_gene_id":"ENSG00000254047.2","gene_symbol":"AC025437.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158188977,"end":158189911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136732.14","gene_symbol":"GYPC","gene_name":"glycophorin C (Gerbich blood group) [Source:HGNC Symbol;Acc:HGNC:4704]","synonyms":"GPC,Ge,CD236R,CD236,GYPD","biotype":"protein_coding","ncbi_id":"2995","summary":"Glycophorin C (GYPC) is an integral membrane glycoprotein. It is a minor species carried by human erythrocytes, but plays an important role in regulating the mechanical stability of red cells. A number of glycophorin C mutations have been described. The Gerbich and Yus phenotypes are due to deletion of exon 3 and 2, respectively. The Webb and Duch antigens, also known as glycophorin D, result from single point mutations of the glycophorin C gene. The glycophorin C protein has very little homology with glycophorins A and B. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":126655933,"end":126696675,"strand":1,"description":"glycophorin C (Gerbich blood group) [Source:HGNC Symbol;Acc:HGNC:4704]"}, {"versioned_ensembl_gene_id":"ENSG00000253673.1","gene_symbol":"AC025437.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158175396,"end":158200016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230115.1","gene_symbol":"TPRG1-AS2","gene_name":"TPRG1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41062]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874027","summary":null,"start":189238686,"end":189240594,"strand":-1,"description":"TPRG1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41062]"}, {"versioned_ensembl_gene_id":"ENSG00000224596.7","gene_symbol":"ZMIZ1-AS1","gene_name":"ZMIZ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27433]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283050","summary":null,"start":78943328,"end":79067895,"strand":-1,"description":"ZMIZ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27433]"}, {"versioned_ensembl_gene_id":"ENSG00000163694.14","gene_symbol":"RBM47","gene_name":"RNA binding motif protein 47 [Source:HGNC Symbol;Acc:HGNC:30358]","synonyms":"NET18,FLJ20273","biotype":"protein_coding","ncbi_id":"54502","summary":null,"start":40423267,"end":40630875,"strand":-1,"description":"RNA binding motif protein 47 [Source:HGNC Symbol;Acc:HGNC:30358]"}, {"versioned_ensembl_gene_id":"ENSG00000253139.1","gene_symbol":"AC013644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56536758,"end":56540497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198482.11","gene_symbol":"ZNF808","gene_name":"zinc finger protein 808 [Source:HGNC Symbol;Acc:HGNC:33230]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388558","summary":null,"start":52527652,"end":52564464,"strand":1,"description":"zinc finger protein 808 [Source:HGNC Symbol;Acc:HGNC:33230]"}, {"versioned_ensembl_gene_id":"ENSG00000258517.1","gene_symbol":"AC004817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71212633,"end":71218216,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230910.2","gene_symbol":"AL391807.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68629962,"end":68635027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246430.6","gene_symbol":"LINC00968","gene_name":"long intergenic non-protein coding RNA 968 [Source:HGNC Symbol;Acc:HGNC:48727]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507632","summary":null,"start":56496246,"end":56559823,"strand":-1,"description":"long intergenic non-protein coding RNA 968 [Source:HGNC Symbol;Acc:HGNC:48727]"}, {"versioned_ensembl_gene_id":"ENSG00000181195.10","gene_symbol":"PENK","gene_name":"proenkephalin [Source:HGNC Symbol;Acc:HGNC:8831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5179","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include the pentapeptide opioids Met-enkephalin and Leu-enkephalin, which are stored in synaptic vesicles, then released into the synapse where they bind to mu- and delta-opioid receptors to modulate the perception of pain. Other non-opioid cleavage products may function in distinct biological activities. [provided by RefSeq, Jul 2015]","start":56436674,"end":56446734,"strand":-1,"description":"proenkephalin [Source:HGNC Symbol;Acc:HGNC:8831]"}, {"versioned_ensembl_gene_id":"ENSG00000148339.12","gene_symbol":"SLC25A25","gene_name":"solute carrier family 25 member 25 [Source:HGNC Symbol;Acc:HGNC:20663]","synonyms":"MCSC,KIAA1896,PCSCL","biotype":"protein_coding","ncbi_id":"114789","summary":"The protein encoded by this gene belongs to the family of calcium-binding mitochondrial carriers, with a characteristic mitochondrial carrier domain at the C-terminus. These proteins are found in the inner membranes of mitochondria, and function as transport proteins. They shuttle metabolites, nucleotides and cofactors through the mitochondrial membrane and thereby connect and/or regulate cytoplasm and matrix functions. This protein may function as an ATP-Mg/Pi carrier that mediates the transport of Mg-ATP in exchange for phosphate, and likely responsible for the net uptake or efflux of adenine nucleotides into or from the mitochondria. Alternatively spliced transcript variants encoding different isoforms with a common C-terminus but variable N-termini have been described for this gene. [provided by RefSeq, Jul 2012]","start":128068201,"end":128109245,"strand":1,"description":"solute carrier family 25 member 25 [Source:HGNC Symbol;Acc:HGNC:20663]"}, {"versioned_ensembl_gene_id":"ENSG00000168754.14","gene_symbol":"FAM178B","gene_name":"family with sequence similarity 178 member B [Source:HGNC Symbol;Acc:HGNC:28036]","synonyms":"LOC51252","biotype":"protein_coding","ncbi_id":"51252","summary":null,"start":96875882,"end":96986592,"strand":-1,"description":"family with sequence similarity 178 member B [Source:HGNC Symbol;Acc:HGNC:28036]"}, {"versioned_ensembl_gene_id":"ENSG00000010310.8","gene_symbol":"GIPR","gene_name":"gastric inhibitory polypeptide receptor [Source:HGNC Symbol;Acc:HGNC:4271]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2696","summary":"This gene encodes a G-protein coupled receptor for gastric inhibitory polypeptide (GIP), which was originally identified as an activity in gut extracts that inhibited gastric acid secretion and gastrin release, but subsequently was demonstrated to stimulate insulin release in the presence of elevated glucose. Mice lacking this gene exhibit higher blood glucose levels with impaired initial insulin response after oral glucose load. Defect in this gene thus may contribute to the pathogenesis of diabetes. [provided by RefSeq, Oct 2011]","start":45668244,"end":45683724,"strand":1,"description":"gastric inhibitory polypeptide receptor [Source:HGNC Symbol;Acc:HGNC:4271]"}, {"versioned_ensembl_gene_id":"ENSG00000166398.12","gene_symbol":"KIAA0355","gene_name":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9710","summary":null,"start":34254537,"end":34355586,"strand":1,"description":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]"}, {"versioned_ensembl_gene_id":"ENSG00000197769.5","gene_symbol":"MAP1LC3C","gene_name":"microtubule associated protein 1 light chain 3 gamma [Source:HGNC Symbol;Acc:HGNC:13353]","synonyms":"ATG8J","biotype":"protein_coding","ncbi_id":"440738","summary":"Autophagy is a highly regulated bulk degradation process that plays an important role in cellular maintenance and development. MAP1LC3C is an ortholog of the yeast autophagosome protein Atg8 (He et al., 2003 [PubMed 12740394]).[supplied by OMIM, Nov 2010]","start":241995490,"end":241999073,"strand":-1,"description":"microtubule associated protein 1 light chain 3 gamma [Source:HGNC Symbol;Acc:HGNC:13353]"}, {"versioned_ensembl_gene_id":"ENSG00000255353.1","gene_symbol":"AP003057.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107176286,"end":107177530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281028.1","gene_symbol":"AC104662.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":25160663,"end":25277306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174429.3","gene_symbol":"ABRA","gene_name":"actin binding Rho activating protein [Source:HGNC Symbol;Acc:HGNC:30655]","synonyms":"STARS","biotype":"protein_coding","ncbi_id":"137735","summary":null,"start":106759483,"end":106770245,"strand":-1,"description":"actin binding Rho activating protein [Source:HGNC Symbol;Acc:HGNC:30655]"}, {"versioned_ensembl_gene_id":"ENSG00000275873.2","gene_symbol":"LMNTD2","gene_name":"lamin tail domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28561]","synonyms":"MGC35138,C11orf35","biotype":"protein_coding","ncbi_id":"256329","summary":null,"start":554854,"end":560793,"strand":-1,"description":"lamin tail domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28561]"}, {"versioned_ensembl_gene_id":"ENSG00000225130.9","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30098021,"end":30108223,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000258894.1","gene_symbol":"AL358913.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43595136,"end":43596683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268316.1","gene_symbol":"AC006272.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51839771,"end":51840945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280385.1","gene_symbol":"AP000648.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90193614,"end":90198120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226840.1","gene_symbol":"PAICSP3","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38096]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780810","summary":null,"start":73327524,"end":73329017,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38096]"}, {"versioned_ensembl_gene_id":"ENSG00000127081.13","gene_symbol":"ZNF484","gene_name":"zinc finger protein 484 [Source:HGNC Symbol;Acc:HGNC:23385]","synonyms":"FLJ33884,BA526D8.4","biotype":"protein_coding","ncbi_id":"83744","summary":null,"start":92845031,"end":92878038,"strand":-1,"description":"zinc finger protein 484 [Source:HGNC Symbol;Acc:HGNC:23385]"}, {"versioned_ensembl_gene_id":"ENSG00000270332.1","gene_symbol":"SMC2-AS1","gene_name":"SMC2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50827]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928550","summary":null,"start":104080024,"end":104093073,"strand":-1,"description":"SMC2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50827]"}, {"versioned_ensembl_gene_id":"ENSG00000229830.1","gene_symbol":"AL589823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103065416,"end":103065598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256937.1","gene_symbol":"KRT17P8","gene_name":"keratin 17 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50726]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130074","summary":null,"start":9127783,"end":9128645,"strand":1,"description":"keratin 17 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50726]"}, {"versioned_ensembl_gene_id":"ENSG00000164442.9","gene_symbol":"CITED2","gene_name":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2 [Source:HGNC Symbol;Acc:HGNC:1987]","synonyms":"MRG1","biotype":"protein_coding","ncbi_id":"10370","summary":"The protein encoded by this gene inhibits transactivation of HIF1A-induced genes by competing with binding of hypoxia-inducible factor 1-alpha to p300-CH1. Mutations in this gene are a cause of cardiac septal defects. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":139371807,"end":139374620,"strand":-1,"description":"Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2 [Source:HGNC Symbol;Acc:HGNC:1987]"}, {"versioned_ensembl_gene_id":"ENSG00000251605.1","gene_symbol":"AC104108.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78307503,"end":78307914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259032.2","gene_symbol":"ENSAP2","gene_name":"endosulfine alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319114","summary":null,"start":82692704,"end":82693055,"strand":-1,"description":"endosulfine alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20011]"}, {"versioned_ensembl_gene_id":"ENSG00000204138.12","gene_symbol":"PHACTR4","gene_name":"phosphatase and actin regulator 4 [Source:HGNC Symbol;Acc:HGNC:25793]","synonyms":"PPP1R124,FLJ13171","biotype":"protein_coding","ncbi_id":"65979","summary":"This gene encodes a member of the phosphatase and actin regulator (PHACTR) family. Other PHACTR family members have been shown to inhibit protein phosphatase 1 (PP1) activity, and the homolog of this gene in the mouse has been shown to interact with actin and PP1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":28369582,"end":28500369,"strand":1,"description":"phosphatase and actin regulator 4 [Source:HGNC Symbol;Acc:HGNC:25793]"}, {"versioned_ensembl_gene_id":"ENSG00000260776.5","gene_symbol":"AC104758.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":77914217,"end":77926846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259384.6","gene_symbol":"GH1","gene_name":"growth hormone 1 [Source:HGNC Symbol;Acc:HGNC:4261]","synonyms":"hGH-N,GHN,GH-N,GH","biotype":"protein_coding","ncbi_id":"2688","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. The five genes share a remarkably high degree of sequence identity. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed in the pituitary but not in placental tissue as is the case for the other four genes in the growth hormone locus. Mutations in or deletions of the gene lead to growth hormone deficiency and short stature. [provided by RefSeq, Jul 2008]","start":63917200,"end":63918838,"strand":-1,"description":"growth hormone 1 [Source:HGNC Symbol;Acc:HGNC:4261]"}, {"versioned_ensembl_gene_id":"ENSG00000241359.1","gene_symbol":"SYNPR-AS1","gene_name":"SYNPR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40774]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874016","summary":null,"start":63423596,"end":63550051,"strand":-1,"description":"SYNPR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40774]"}, {"versioned_ensembl_gene_id":"ENSG00000219073.7","gene_symbol":"CELA3B","gene_name":"chymotrypsin like elastase family member 3B [Source:HGNC Symbol;Acc:HGNC:15945]","synonyms":"ELA3B,CBPP","biotype":"protein_coding","ncbi_id":"23436","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Unlike other elastases, elastase 3B has little elastolytic activity. Like most of the human elastases, elastase 3B is secreted from the pancreas as a zymogen and, like other serine proteases such as trypsin, chymotrypsin and kallikrein, it has a digestive function in the intestine. Elastase 3B preferentially cleaves proteins after alanine residues. Elastase 3B may also function in the intestinal transport and metabolism of cholesterol. Both elastase 3A and elastase 3B have been referred to as protease E and as elastase 1, and excretion of this protein in fecal material is frequently used as a measure of pancreatic function in clinical assays. [provided by RefSeq, May 2009]","start":21977021,"end":21998642,"strand":1,"description":"chymotrypsin like elastase family member 3B [Source:HGNC Symbol;Acc:HGNC:15945]"}, {"versioned_ensembl_gene_id":"ENSG00000259333.1","gene_symbol":"AC127029.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63900643,"end":63900879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268797.1","gene_symbol":"AC008537.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":40801297,"end":40898282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269843.1","gene_symbol":"AC008537.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40831221,"end":40837210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257622.1","gene_symbol":"AL512356.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":105152194,"end":105181194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258975.1","gene_symbol":"AL133279.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88136733,"end":88159845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140950.15","gene_symbol":"TLDC1","gene_name":"TBC/LysM-associated domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29325]","synonyms":"KIAA1609","biotype":"protein_coding","ncbi_id":"57707","summary":null,"start":84476421,"end":84554033,"strand":-1,"description":"TBC/LysM-associated domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29325]"}, {"versioned_ensembl_gene_id":"ENSG00000260139.6","gene_symbol":"CSPG4P13","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49195]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100302666","summary":null,"start":77894684,"end":77904674,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49195]"}, {"versioned_ensembl_gene_id":"ENSG00000259783.5","gene_symbol":"LINC02259","gene_name":"long intergenic non-protein coding RNA 2259 [Source:HGNC Symbol;Acc:HGNC:53172]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723640","summary":null,"start":72608481,"end":72636919,"strand":-1,"description":"long intergenic non-protein coding RNA 2259 [Source:HGNC Symbol;Acc:HGNC:53172]"}, {"versioned_ensembl_gene_id":"ENSG00000211828.1","gene_symbol":"TRDJ3","gene_name":"T-cell receptor delta joining 3 [Source:HGNC Symbol;Acc:HGNC:12259]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28520","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22459098,"end":22459156,"strand":1,"description":"T-cell receptor delta joining 3 [Source:HGNC Symbol;Acc:HGNC:12259]"}, {"versioned_ensembl_gene_id":"ENSG00000211832.2","gene_symbol":"TRAJ59","gene_name":"T-cell receptor alpha joining 59 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12091]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28696","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22476553,"end":22476606,"strand":1,"description":"T-cell receptor alpha joining 59 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12091]"}, {"versioned_ensembl_gene_id":"ENSG00000275139.1","gene_symbol":"AL133492.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45759804,"end":45763758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228985.1","gene_symbol":"TRDD3","gene_name":"T-cell receptor delta diversity 3 [Source:HGNC Symbol;Acc:HGNC:12256]","synonyms":null,"biotype":"TR_D_gene","ncbi_id":"28523","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22449113,"end":22449125,"strand":1,"description":"T-cell receptor delta diversity 3 [Source:HGNC Symbol;Acc:HGNC:12256]"}, {"versioned_ensembl_gene_id":"ENSG00000251228.1","gene_symbol":"AC104619.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134944275,"end":134944523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180423.4","gene_symbol":"HARBI1","gene_name":"harbinger transposase derived 1 [Source:HGNC Symbol;Acc:HGNC:26522]","synonyms":"FLJ32675,C11orf77","biotype":"protein_coding","ncbi_id":"283254","summary":null,"start":46602861,"end":46617909,"strand":-1,"description":"harbinger transposase derived 1 [Source:HGNC Symbol;Acc:HGNC:26522]"}, {"versioned_ensembl_gene_id":"ENSG00000196976.7","gene_symbol":"LAGE3","gene_name":"L antigen family member 3 [Source:HGNC Symbol;Acc:HGNC:26058]","synonyms":"Pcc1,ITBA2,ESO3,DXS9951E,DXS9879E,CVG5","biotype":"protein_coding","ncbi_id":"8270","summary":"This gene belongs to the ESO/LAGE gene family, members of which are clustered together on chromosome Xq28, and have similar exon-intron structures. Unlike the other family members which are normally expressed only in testis and activated in a wide range of human tumors, this gene is ubiquitously expressed in somatic tissues. The latter, combined with the finding that it is highly conserved in mouse and rat, suggests that the encoded protein is functionally important. An intronless pseudogene with high sequence similarity to this gene is located on chromosome 9. [provided by RefSeq, Jul 2008]","start":154477769,"end":154479257,"strand":-1,"description":"L antigen family member 3 [Source:HGNC Symbol;Acc:HGNC:26058]"}, {"versioned_ensembl_gene_id":"ENSG00000258841.1","gene_symbol":"EEF1A1P2","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319112","summary":null,"start":81661428,"end":81662874,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20008]"}, {"versioned_ensembl_gene_id":"ENSG00000251259.1","gene_symbol":"AC004069.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105137280,"end":105140619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231340.1","gene_symbol":"ACTG1P10","gene_name":"actin gamma 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:155]","synonyms":"ACTGP10,ACTL1","biotype":"processed_pseudogene","ncbi_id":"83","summary":null,"start":53142832,"end":53143913,"strand":-1,"description":"actin gamma 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:155]"}, {"versioned_ensembl_gene_id":"ENSG00000232242.2","gene_symbol":"ZYG11AP1","gene_name":"zyg-11 family member A, cell cycle regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131879","summary":null,"start":102611162,"end":102612155,"strand":-1,"description":"zyg-11 family member A, cell cycle regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38032]"}, {"versioned_ensembl_gene_id":"ENSG00000233921.2","gene_symbol":"RPS15AP40","gene_name":"ribosomal protein S15a pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36041]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128083","summary":null,"start":36374793,"end":36375183,"strand":-1,"description":"ribosomal protein S15a pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36041]"}, {"versioned_ensembl_gene_id":"ENSG00000100604.12","gene_symbol":"CHGA","gene_name":"chromogranin A [Source:HGNC Symbol;Acc:HGNC:1929]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1113","summary":"The protein encoded by this gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. It is found in secretory vesicles of neurons and endocrine cells. This gene product is a precursor to three biologically active peptides; vasostatin, pancreastatin, and parastatin. These peptides act as autocrine or paracrine negative modulators of the neuroendocrine system. Two other peptides, catestatin and chromofungin, have antimicrobial activity and antifungal activity, respectively. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":92923080,"end":92935293,"strand":1,"description":"chromogranin A [Source:HGNC Symbol;Acc:HGNC:1929]"}, {"versioned_ensembl_gene_id":"ENSG00000102181.20","gene_symbol":"CD99L2","gene_name":"CD99 molecule like 2 [Source:HGNC Symbol;Acc:HGNC:18237]","synonyms":"MIC2L1,CD99B","biotype":"protein_coding","ncbi_id":"83692","summary":"This gene encodes a cell-surface protein that is similar to CD99. A similar protein in mouse functions as an adhesion molecule during leukocyte extravasation. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":150766337,"end":150898816,"strand":-1,"description":"CD99 molecule like 2 [Source:HGNC Symbol;Acc:HGNC:18237]"}, {"versioned_ensembl_gene_id":"ENSG00000169783.12","gene_symbol":"LINGO1","gene_name":"leucine rich repeat and Ig domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21205]","synonyms":"LRRN6A,LERN1,FLJ14594","biotype":"protein_coding","ncbi_id":"84894","summary":null,"start":77613027,"end":77820900,"strand":-1,"description":"leucine rich repeat and Ig domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21205]"}, {"versioned_ensembl_gene_id":"ENSG00000164440.14","gene_symbol":"TXLNB","gene_name":"taxilin beta [Source:HGNC Symbol;Acc:HGNC:21617]","synonyms":"dJ522B19.2,C6orf198,MDP77,DKFZp451A175","biotype":"protein_coding","ncbi_id":"167838","summary":null,"start":139240061,"end":139292139,"strand":-1,"description":"taxilin beta [Source:HGNC Symbol;Acc:HGNC:21617]"}, {"versioned_ensembl_gene_id":"ENSG00000171102.14","gene_symbol":"OBP2B","gene_name":"odorant binding protein 2B [Source:HGNC Symbol;Acc:HGNC:23381]","synonyms":"LCN14,hOBPIIb","biotype":"protein_coding","ncbi_id":"29989","summary":null,"start":133205277,"end":133209250,"strand":-1,"description":"odorant binding protein 2B [Source:HGNC Symbol;Acc:HGNC:23381]"}, {"versioned_ensembl_gene_id":"ENSG00000223626.1","gene_symbol":"LINC01044","gene_name":"long intergenic non-protein coding RNA 1044 [Source:HGNC Symbol;Acc:HGNC:49032]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266956","summary":null,"start":112322567,"end":112331225,"strand":-1,"description":"long intergenic non-protein coding RNA 1044 [Source:HGNC Symbol;Acc:HGNC:49032]"}, {"versioned_ensembl_gene_id":"ENSG00000124743.5","gene_symbol":"KLHL31","gene_name":"kelch like family member 31 [Source:HGNC Symbol;Acc:HGNC:21353]","synonyms":"KBTBD1,BKLHD6,bA345L23.2","biotype":"protein_coding","ncbi_id":"401265","summary":null,"start":53647901,"end":53665708,"strand":-1,"description":"kelch like family member 31 [Source:HGNC Symbol;Acc:HGNC:21353]"}, {"versioned_ensembl_gene_id":"ENSG00000085449.14","gene_symbol":"WDFY1","gene_name":"WD repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20451]","synonyms":"ZFYVE17,WDF1,KIAA1435,FENS-1","biotype":"protein_coding","ncbi_id":"57590","summary":"The protein encoded by this gene is a phosphatidylinositol 3-phosphate binding protein, which contains a FYVE zinc finger domain and multiple WD-40 repeat domains. When exogenously expressed, it localizes to early endosomes. Mutagenesis analysis demonstrates that this endosomal localization is mediated by the FYVE domain. [provided by RefSeq, Jan 2015]","start":223855716,"end":223945387,"strand":-1,"description":"WD repeat and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20451]"}, {"versioned_ensembl_gene_id":"ENSG00000211813.2","gene_symbol":"TRAV34","gene_name":"T-cell receptor alpha variable 34 [Source:HGNC Symbol;Acc:HGNC:12133]","synonyms":"TCRAV34S1,TCRAV26S1","biotype":"TR_V_gene","ncbi_id":"28648","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22207522,"end":22208129,"strand":1,"description":"T-cell receptor alpha variable 34 [Source:HGNC Symbol;Acc:HGNC:12133]"}, {"versioned_ensembl_gene_id":"ENSG00000089127.12","gene_symbol":"OAS1","gene_name":"2'-5'-oligoadenylate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:8086]","synonyms":"IFI-4,OIASI,OIAS","biotype":"protein_coding","ncbi_id":"4938","summary":"This gene is induced by interferons and encodes a protein that synthesizes 2',5'-oligoadenylates (2-5As). This protein activates latent RNase L, which results in viral RNA degradation and the inhibition of viral replication. Alternative splicing results in multiple transcript variants with different enzymatic activities. Polymorphisms in this gene have been associated with susceptibility to viral infection and diabetes mellitus, type 1. A disease-associated allele in a splice acceptor site influences the production of the p46 splice isoform. This gene is located in a cluster of related genes on chromosome 12. [provided by RefSeq, Feb 2016]","start":112906777,"end":112933222,"strand":1,"description":"2'-5'-oligoadenylate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:8086]"}, {"versioned_ensembl_gene_id":"ENSG00000282413.1","gene_symbol":"AL133461.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119818866,"end":119819133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276217.2","gene_symbol":"TAS2R15P","gene_name":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]","synonyms":"T2R15,PS8,TAS2R15","biotype":"processed_pseudogene","ncbi_id":"266657","summary":null,"start":10964425,"end":10965352,"strand":-1,"description":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]"}, {"versioned_ensembl_gene_id":"ENSG00000186234.7","gene_symbol":"FAM86MP","gene_name":"family with sequence similarity 86 member M, pseudogene [Source:HGNC Symbol;Acc:HGNC:44100]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644517","summary":null,"start":9692495,"end":9702954,"strand":1,"description":"family with sequence similarity 86 member M, pseudogene [Source:HGNC Symbol;Acc:HGNC:44100]"}, {"versioned_ensembl_gene_id":"ENSG00000267610.2","gene_symbol":"AC007787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13069792,"end":13071374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227583.1","gene_symbol":"RPS3AP37","gene_name":"ribosomal protein S3a pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36691]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271593","summary":null,"start":68674356,"end":68675100,"strand":1,"description":"ribosomal protein S3a pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36691]"}, {"versioned_ensembl_gene_id":"ENSG00000268777.1","gene_symbol":"AC020914.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51519731,"end":51520260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109790.16","gene_symbol":"KLHL5","gene_name":"kelch like family member 5 [Source:HGNC Symbol;Acc:HGNC:6356]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51088","summary":null,"start":39045039,"end":39126857,"strand":1,"description":"kelch like family member 5 [Source:HGNC Symbol;Acc:HGNC:6356]"}, {"versioned_ensembl_gene_id":"ENSG00000133997.11","gene_symbol":"MED6","gene_name":"mediator complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:19970]","synonyms":"NY-REN-28","biotype":"protein_coding","ncbi_id":"10001","summary":null,"start":70581257,"end":70600690,"strand":-1,"description":"mediator complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:19970]"}, {"versioned_ensembl_gene_id":"ENSG00000172687.13","gene_symbol":"ZNF738","gene_name":"zinc finger protein 738 [Source:HGNC Symbol;Acc:HGNC:32469]","synonyms":null,"biotype":"protein_coding","ncbi_id":"148203","summary":null,"start":21358930,"end":21379302,"strand":1,"description":"zinc finger protein 738 [Source:HGNC Symbol;Acc:HGNC:32469]"}, {"versioned_ensembl_gene_id":"ENSG00000166428.12","gene_symbol":"PLD4","gene_name":"phospholipase D family member 4 [Source:HGNC Symbol;Acc:HGNC:23792]","synonyms":"C14orf175","biotype":"protein_coding","ncbi_id":"122618","summary":null,"start":104924816,"end":104937790,"strand":1,"description":"phospholipase D family member 4 [Source:HGNC Symbol;Acc:HGNC:23792]"}, {"versioned_ensembl_gene_id":"ENSG00000251624.1","gene_symbol":"UNC93B7","gene_name":"unc-93 homolog B7 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:44036]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100887746","summary":null,"start":9493736,"end":9498066,"strand":1,"description":"unc-93 homolog B7 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:44036]"}, {"versioned_ensembl_gene_id":"ENSG00000242279.1","gene_symbol":"AP000893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82957423,"end":82958216,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187994.13","gene_symbol":"RINL","gene_name":"Ras and Rab interactor like [Source:HGNC Symbol;Acc:HGNC:24795]","synonyms":"FLJ45909","biotype":"protein_coding","ncbi_id":"126432","summary":null,"start":38867834,"end":38878279,"strand":-1,"description":"Ras and Rab interactor like [Source:HGNC Symbol;Acc:HGNC:24795]"}, {"versioned_ensembl_gene_id":"ENSG00000151689.12","gene_symbol":"INPP1","gene_name":"inositol polyphosphate-1-phosphatase [Source:HGNC Symbol;Acc:HGNC:6071]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3628","summary":"This gene encodes the enzyme inositol polyphosphate-1-phosphatase, one of the enzymes involved in phosphatidylinositol signaling pathways. This enzyme removes the phosphate group at position 1 of the inositol ring from the polyphosphates inositol 1,4-bisphosphate and inositol 1,3,4-trisphophosphate. [provided by RefSeq, Jul 2008]","start":190343470,"end":190371665,"strand":1,"description":"inositol polyphosphate-1-phosphatase [Source:HGNC Symbol;Acc:HGNC:6071]"}, {"versioned_ensembl_gene_id":"ENSG00000224319.4","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587555,"end":29589138,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000250241.5","gene_symbol":"AC105383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133075311,"end":133149116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239413.1","gene_symbol":"RPS27P23","gene_name":"ribosomal protein S27 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130775","summary":null,"start":101424441,"end":101424691,"strand":1,"description":"ribosomal protein S27 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35716]"}, {"versioned_ensembl_gene_id":"ENSG00000235510.1","gene_symbol":"BX842568.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36957913,"end":36958139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157005.3","gene_symbol":"SST","gene_name":"somatostatin [Source:HGNC Symbol;Acc:HGNC:11329]","synonyms":"SMST","biotype":"protein_coding","ncbi_id":"6750","summary":"The hormone somatostatin has active 14 aa and 28 aa forms that are produced by alternate cleavage of the single preproprotein encoded by this gene. Somatostatin is expressed throughout the body and inhibits the release of numerous secondary hormones by binding to high-affinity G-protein-coupled somatostatin receptors. This hormone is an important regulator of the endocrine system through its interactions with pituitary growth hormone, thyroid stimulating hormone, and most hormones of the gastrointestinal tract. Somatostatin also affects rates of neurotransmission in the central nervous system and proliferation of both normal and tumorigenic cells. [provided by RefSeq, Jul 2008]","start":187668906,"end":187670399,"strand":-1,"description":"somatostatin [Source:HGNC Symbol;Acc:HGNC:11329]"}, {"versioned_ensembl_gene_id":"ENSG00000228952.1","gene_symbol":"LINC02041","gene_name":"long intergenic non-protein coding RNA 2041 [Source:HGNC Symbol;Acc:HGNC:52881]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374261","summary":null,"start":187448845,"end":187449450,"strand":1,"description":"long intergenic non-protein coding RNA 2041 [Source:HGNC Symbol;Acc:HGNC:52881]"}, {"versioned_ensembl_gene_id":"ENSG00000268861.6","gene_symbol":"AC008878.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7382834,"end":7472477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146834.13","gene_symbol":"MEPCE","gene_name":"methylphosphate capping enzyme [Source:HGNC Symbol;Acc:HGNC:20247]","synonyms":"MePCE,FLJ20257,BCDIN3","biotype":"protein_coding","ncbi_id":"56257","summary":null,"start":100428790,"end":100434126,"strand":1,"description":"methylphosphate capping enzyme [Source:HGNC Symbol;Acc:HGNC:20247]"}, {"versioned_ensembl_gene_id":"ENSG00000224163.4","gene_symbol":"AC025594.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128912732,"end":128914063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000025293.16","gene_symbol":"PHF20","gene_name":"PHD finger protein 20 [Source:HGNC Symbol;Acc:HGNC:16098]","synonyms":"TDRD20A,dJ1121G12.1,C20orf104","biotype":"protein_coding","ncbi_id":"51230","summary":null,"start":35771974,"end":35950381,"strand":1,"description":"PHD finger protein 20 [Source:HGNC Symbol;Acc:HGNC:16098]"}, {"versioned_ensembl_gene_id":"ENSG00000230972.1","gene_symbol":"AP001116.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23065491,"end":23131206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261151.1","gene_symbol":"AC012182.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58092053,"end":58092947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231058.1","gene_symbol":"MSANTD2P1","gene_name":"Myb/SANT DNA binding domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39637]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130310","summary":null,"start":23101223,"end":23103074,"strand":1,"description":"Myb/SANT DNA binding domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39637]"}, {"versioned_ensembl_gene_id":"ENSG00000105366.15","gene_symbol":"SIGLEC8","gene_name":"sialic acid binding Ig like lectin 8 [Source:HGNC Symbol;Acc:HGNC:10877]","synonyms":"SIGLEC8L,SIGLEC-8,SAF2,MGC59785","biotype":"protein_coding","ncbi_id":"27181","summary":"Sialic acid-binding immunoglobulin (Ig)-like lectins, or SIGLECs (e.g., CD33 (MIM 159590)), are a family of type 1 transmembrane proteins each having a unique expression pattern, mostly in hemopoietic cells. SIGLEC8 is a member of the CD33-like subgroup of SIGLECs, which are localized to 19q13.3-q13.4 and have 2 conserved cytoplasmic tyrosine-based motifs: an immunoreceptor tyrosine-based inhibitory motif, or ITIM (see MIM 604964), and a motif homologous to one identified in signaling lymphocyte activation molecule (SLAM; MIM 603492) that mediates an association with SLAM-associated protein (SAP; MIM 300490) (summarized by Foussias et al., 2000 [PubMed 11095983]).[supplied by OMIM, May 2010]","start":51450847,"end":51458456,"strand":-1,"description":"sialic acid binding Ig like lectin 8 [Source:HGNC Symbol;Acc:HGNC:10877]"}, {"versioned_ensembl_gene_id":"ENSG00000225308.2","gene_symbol":"ASS1P11","gene_name":"argininosuccinate synthetase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:761]","synonyms":"TCAG_1641141,ASSP11","biotype":"processed_pseudogene","ncbi_id":"340274","summary":null,"start":21220213,"end":21221428,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:761]"}, {"versioned_ensembl_gene_id":"ENSG00000234034.1","gene_symbol":"AP000959.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22500604,"end":22520058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184178.15","gene_symbol":"SCFD2","gene_name":"sec1 family domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30676]","synonyms":"STXBP1L1,FLJ39514","biotype":"protein_coding","ncbi_id":"152579","summary":null,"start":52872982,"end":53366075,"strand":-1,"description":"sec1 family domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30676]"}, {"versioned_ensembl_gene_id":"ENSG00000177683.13","gene_symbol":"THAP5","gene_name":"THAP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23188]","synonyms":"DKFZp313O1132","biotype":"protein_coding","ncbi_id":"168451","summary":null,"start":108554543,"end":108569750,"strand":-1,"description":"THAP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23188]"}, {"versioned_ensembl_gene_id":"ENSG00000196183.5","gene_symbol":"RPS2P4","gene_name":"ribosomal protein S2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19814]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"92427","summary":null,"start":104835997,"end":104836852,"strand":-1,"description":"ribosomal protein S2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:19814]"}, {"versioned_ensembl_gene_id":"ENSG00000262358.1","gene_symbol":"AC116914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3729361,"end":3730493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253493.1","gene_symbol":"AC087808.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64973488,"end":64973848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136111.12","gene_symbol":"TBC1D4","gene_name":"TBC1 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:19165]","synonyms":"KIAA0603,DKFZp779C0666,AS160","biotype":"protein_coding","ncbi_id":"9882","summary":"This gene is a member of the Tre-2/BUB2/CDC16 domain family. The protein encoded by this gene is a Rab-GTPase-activating protein, and contains two phopshotyrosine-binding domains (PTB1 and PTB2), a calmodulin-binding domain (CBD), a Rab-GTPase domain, and multiple AKT phosphomotifs. This protein is thought to play an important role in glucose homeostasis by regulating the insulin-dependent trafficking of the glucose transporter 4 (GLUT4), important for removing glucose from the bloodstream into skeletal muscle and fat tissues. Reduced expression of this gene results in an increase in GLUT4 levels at the plasma membrane, suggesting that this protein is important in intracellular retention of GLUT4 under basal conditions. When exposed to insulin, this protein is phosphorylated, dissociates from GLUT4 vesicles, resulting in increased GLUT4 at the cell surface, and enhanced glucose transport. Phosphorylation of this protein by AKT is required for proper translocation of GLUT4 to the cell surface. Individuals homozygous for a mutation in this gene are at higher risk for type 2 diabetes and have higher levels of circulating glucose and insulin levels after glucose ingestion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":75284665,"end":75482114,"strand":-1,"description":"TBC1 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:19165]"}, {"versioned_ensembl_gene_id":"ENSG00000187689.9","gene_symbol":"AMTN","gene_name":"amelotin [Source:HGNC Symbol;Acc:HGNC:33188]","synonyms":"UNQ689,RSTI689","biotype":"protein_coding","ncbi_id":"401138","summary":"The mineralized portions of teeth, the dentin and enamel, are formed by mesenchyme-derived odontoblasts and epithelium-derived ameloblasts, respectively. As ameloblasts differentiate, they deposit specific proteins necessary for enamel formation, including amelogenin (AMELX; MIM 300391), enamelin (ENAM; MIM 606585), and ameloblastin (AMBN; MIM 601259), in the organic enamel matrix. Amelotin is specifically expressed in maturation-stage ameloblasts (Iwasaki et al., 2005 [PubMed 16304441]).[supplied by OMIM, Mar 2008]","start":70518540,"end":70532742,"strand":1,"description":"amelotin [Source:HGNC Symbol;Acc:HGNC:33188]"}, {"versioned_ensembl_gene_id":"ENSG00000271079.1","gene_symbol":"CTAGE15","gene_name":"CTAGE family member 15 [Source:HGNC Symbol;Acc:HGNC:37295]","synonyms":"CTAGE15P","biotype":"protein_coding","ncbi_id":"441294","summary":null,"start":143571801,"end":143574387,"strand":1,"description":"CTAGE family member 15 [Source:HGNC Symbol;Acc:HGNC:37295]"}, {"versioned_ensembl_gene_id":"ENSG00000265261.1","gene_symbol":"AC027575.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76884935,"end":76888724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232740.1","gene_symbol":"LINC01826","gene_name":"long intergenic non-protein coding RNA 1826 [Source:HGNC Symbol;Acc:HGNC:52632]","synonyms":"lnc-MKI67IP-3","biotype":"lincRNA","ncbi_id":"107985818","summary":null,"start":123066151,"end":123073481,"strand":-1,"description":"long intergenic non-protein coding RNA 1826 [Source:HGNC Symbol;Acc:HGNC:52632]"}, {"versioned_ensembl_gene_id":"ENSG00000019169.10","gene_symbol":"MARCO","gene_name":"macrophage receptor with collagenous structure [Source:HGNC Symbol;Acc:HGNC:6895]","synonyms":"SR-A6,SCARA2","biotype":"protein_coding","ncbi_id":"8685","summary":"The protein encoded by this gene is a member of the class A scavenger receptor family and is part of the innate antimicrobial immune system. The protein may bind both Gram-negative and Gram-positive bacteria via an extracellular, C-terminal, scavenger receptor cysteine-rich (SRCR) domain. In addition to short cytoplasmic and transmembrane domains, there is an extracellular spacer domain and a long, extracellular collagenous domain. The protein may form a trimeric molecule by the association of the collagenous domains of three identical polypeptide chains. [provided by RefSeq, Jul 2008]","start":118942166,"end":118994660,"strand":1,"description":"macrophage receptor with collagenous structure [Source:HGNC Symbol;Acc:HGNC:6895]"}, {"versioned_ensembl_gene_id":"ENSG00000187801.14","gene_symbol":"ZFP69B","gene_name":"ZFP69 zinc finger protein B [Source:HGNC Symbol;Acc:HGNC:28053]","synonyms":"ZSCAN54B,ZNF643,ZKSCAN23B,FLJ34293","biotype":"protein_coding","ncbi_id":"65243","summary":null,"start":40450102,"end":40463718,"strand":1,"description":"ZFP69 zinc finger protein B [Source:HGNC Symbol;Acc:HGNC:28053]"}, {"versioned_ensembl_gene_id":"ENSG00000227088.1","gene_symbol":"AC084149.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77652413,"end":77654668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232356.1","gene_symbol":"CR388393.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497439,"end":29510486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272668.1","gene_symbol":"AL590560.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159866954,"end":159867685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165417.11","gene_symbol":"GTF2A1","gene_name":"general transcription factor IIA subunit 1 [Source:HGNC Symbol;Acc:HGNC:4646]","synonyms":"TFIIA","biotype":"protein_coding","ncbi_id":"2957","summary":"Accurate transcription initiation on TATA-containing class II genes involves the ordered assembly of RNA polymerase II (POLR2A; MIM 180660) and several general initiation factors (summarized by DeJong and Roeder, 1993 [PubMed 8224848]). One of these factors is TFIIA, which when purified from HeLa extracts consists of 35-, 19-, and 12-kD subunits.[supplied by OMIM, Jul 2010]","start":81175452,"end":81221377,"strand":-1,"description":"general transcription factor IIA subunit 1 [Source:HGNC Symbol;Acc:HGNC:4646]"}, {"versioned_ensembl_gene_id":"ENSG00000228515.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486696,"end":29487832,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000259188.5","gene_symbol":"AC025040.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49879604,"end":49883525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257475.2","gene_symbol":"AC068888.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53012104,"end":53013921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213301.2","gene_symbol":"HMGB3P11","gene_name":"high mobility group box 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39303]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644442","summary":null,"start":104771282,"end":104771885,"strand":1,"description":"high mobility group box 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39303]"}, {"versioned_ensembl_gene_id":"ENSG00000249736.1","gene_symbol":"LINC02242","gene_name":"long intergenic non-protein coding RNA 2242 [Source:HGNC Symbol;Acc:HGNC:53127]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379006","summary":null,"start":67632266,"end":67646789,"strand":-1,"description":"long intergenic non-protein coding RNA 2242 [Source:HGNC Symbol;Acc:HGNC:53127]"}, {"versioned_ensembl_gene_id":"ENSG00000250421.5","gene_symbol":"AC106798.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67699429,"end":67902600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261054.1","gene_symbol":"AC036108.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99128832,"end":99131806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279904.1","gene_symbol":"AC068057.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":104706612,"end":104707506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232984.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457111,"end":29464258,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000237588.2","gene_symbol":"AL590666.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156687695,"end":156691997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213155.4","gene_symbol":"AC007547.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181866351,"end":181867154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163006.11","gene_symbol":"CCDC138","gene_name":"coiled-coil domain containing 138 [Source:HGNC Symbol;Acc:HGNC:26531]","synonyms":"FLJ32745","biotype":"protein_coding","ncbi_id":"165055","summary":null,"start":108786757,"end":108885477,"strand":1,"description":"coiled-coil domain containing 138 [Source:HGNC Symbol;Acc:HGNC:26531]"}, {"versioned_ensembl_gene_id":"ENSG00000233334.3","gene_symbol":"FAM53B-AS1","gene_name":"FAM53B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49499]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927944","summary":null,"start":124703625,"end":124714217,"strand":1,"description":"FAM53B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49499]"}, {"versioned_ensembl_gene_id":"ENSG00000178917.15","gene_symbol":"ZNF852","gene_name":"zinc finger protein 852 [Source:HGNC Symbol;Acc:HGNC:27713]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285346","summary":null,"start":44498970,"end":44510636,"strand":-1,"description":"zinc finger protein 852 [Source:HGNC Symbol;Acc:HGNC:27713]"}, {"versioned_ensembl_gene_id":"ENSG00000258466.5","gene_symbol":"AL049779.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":67659820,"end":67690367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112462.8","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29373423,"end":29375291,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000072042.12","gene_symbol":"RDH11","gene_name":"retinol dehydrogenase 11 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:17964]","synonyms":"SDR7C1,MDT1,ARSDR1","biotype":"protein_coding","ncbi_id":"51109","summary":"The protein encoded by this gene is an NADPH-dependent retinal reductase and a short-chain dehydrogenase/reductase. The encoded protein has no steroid dehydrogenase activity. [provided by RefSeq, Nov 2011]","start":67676801,"end":67695814,"strand":-1,"description":"retinol dehydrogenase 11 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:17964]"}, {"versioned_ensembl_gene_id":"ENSG00000217786.1","gene_symbol":"AL355379.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79326568,"end":79327207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273033.2","gene_symbol":"LINC02035","gene_name":"long intergenic non-protein coding RNA 2035 [Source:HGNC Symbol;Acc:HGNC:52875]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129550","summary":null,"start":122886941,"end":122892416,"strand":1,"description":"long intergenic non-protein coding RNA 2035 [Source:HGNC Symbol;Acc:HGNC:52875]"}, {"versioned_ensembl_gene_id":"ENSG00000138615.5","gene_symbol":"CILP","gene_name":"cartilage intermediate layer protein [Source:HGNC Symbol;Acc:HGNC:1980]","synonyms":"HsT18872","biotype":"protein_coding","ncbi_id":"8483","summary":"Major alterations in the composition of the cartilage extracellular matrix occur in joint disease, such as osteoarthrosis. This gene encodes the cartilage intermediate layer protein (CILP), which increases in early osteoarthrosis cartilage. The encoded protein was thought to encode a protein precursor for two different proteins; an N-terminal CILP and a C-terminal homolog of NTPPHase, however, later studies identified no nucleotide pyrophosphatase phosphodiesterase (NPP) activity. The full-length and the N-terminal domain of this protein was shown to function as an IGF-1 antagonist. An allelic variant of this gene has been associated with lumbar disc disease. [provided by RefSeq, Sep 2010]","start":65194758,"end":65211488,"strand":-1,"description":"cartilage intermediate layer protein [Source:HGNC Symbol;Acc:HGNC:1980]"}, {"versioned_ensembl_gene_id":"ENSG00000237929.1","gene_symbol":"RPL31P3","gene_name":"ribosomal protein L31 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16549]","synonyms":"dJ1018D12.4","biotype":"processed_pseudogene","ncbi_id":"140718","summary":null,"start":31311303,"end":31311962,"strand":-1,"description":"ribosomal protein L31 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16549]"}, {"versioned_ensembl_gene_id":"ENSG00000204695.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29301701,"end":29313017,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000277150.1","gene_symbol":"F8A3","gene_name":"coagulation factor VIII associated 3 [Source:HGNC Symbol;Acc:HGNC:31850]","synonyms":null,"biotype":"protein_coding","ncbi_id":"474384","summary":"This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the most telomeric copy. Although its function is unknown, the observation that this gene is conserved in the mouse implies it has some function. Unlike factor VIII, this gene is transcribed abundantly in a wide variety of cell types. [provided by RefSeq, Jul 2008]","start":155456914,"end":155458672,"strand":-1,"description":"coagulation factor VIII associated 3 [Source:HGNC Symbol;Acc:HGNC:31850]"}, {"versioned_ensembl_gene_id":"ENSG00000274791.1","gene_symbol":"F8A2","gene_name":"coagulation factor VIII associated 2 [Source:HGNC Symbol;Acc:HGNC:31849]","synonyms":null,"biotype":"protein_coding","ncbi_id":"474383","summary":"This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the middle copy. Although its function is unknown, the observation that this gene is conserved in the mouse implies it has some function. Unlike factor VIII, this gene is transcribed abundantly in a wide variety of cell types. [provided by RefSeq, Jul 2008]","start":155382115,"end":155383230,"strand":1,"description":"coagulation factor VIII associated 2 [Source:HGNC Symbol;Acc:HGNC:31849]"}, {"versioned_ensembl_gene_id":"ENSG00000276612.3","gene_symbol":"FP565260.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5116343,"end":5133805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279196.1","gene_symbol":"AC135048.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30984630,"end":30988270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099381.17","gene_symbol":"SETD1A","gene_name":"SET domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29010]","synonyms":"KMT2F,KIAA0339,Set1","biotype":"protein_coding","ncbi_id":"9739","summary":"The protein encoded by this gene is a component of a histone methyltransferase (HMT) complex that produces mono-, di-, and trimethylated histone H3 at Lys4. Trimethylation of histone H3 at lysine 4 (H3K4me3) is a chromatin modification known to generally mark the transcription start sites of active genes. The protein contains SET domains, a RNA recognition motif domain and is a member of the class V-like SAM-binding methyltransferase superfamily. [provided by RefSeq, Dec 2016]","start":30957294,"end":30984664,"strand":1,"description":"SET domain containing 1A [Source:HGNC Symbol;Acc:HGNC:29010]"}, {"versioned_ensembl_gene_id":"ENSG00000228652.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044178,"end":29045205,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000230238.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29785254,"end":29791477,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000229356.1","gene_symbol":"LRRC3-AS1","gene_name":"LRRC3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43636]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861510","summary":null,"start":44450986,"end":44455284,"strand":-1,"description":"LRRC3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43636]"}, {"versioned_ensembl_gene_id":"ENSG00000254760.1","gene_symbol":"AC008750.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51414298,"end":51414965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116237.15","gene_symbol":"ICMT","gene_name":"isoprenylcysteine carboxyl methyltransferase [Source:HGNC Symbol;Acc:HGNC:5350]","synonyms":"PPMT,PCCMT,HSTE14","biotype":"protein_coding","ncbi_id":"23463","summary":"This gene encodes the third of three enzymes that posttranslationally modify isoprenylated C-terminal cysteine residues in certain proteins and target those proteins to the cell membrane. This enzyme localizes to the endoplasmic reticulum. Alternative splicing may result in other transcript variants, but the biological validity of those transcripts has not been determined. [provided by RefSeq, Jul 2008]","start":6221193,"end":6235972,"strand":-1,"description":"isoprenylcysteine carboxyl methyltransferase [Source:HGNC Symbol;Acc:HGNC:5350]"}, {"versioned_ensembl_gene_id":"ENSG00000228912.2","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29744691,"end":29745111,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000136485.14","gene_symbol":"DCAF7","gene_name":"DDB1 and CUL4 associated factor 7 [Source:HGNC Symbol;Acc:HGNC:30915]","synonyms":"WDR68,SWAN-1,HAN11","biotype":"protein_coding","ncbi_id":"10238","summary":"This gene encodes a protein with multiple WD40 repeats which facilitate protein-protein interactions and thereby enable the assembly of multiprotein complexes. This protein has been shown to function as a scaffold protein for protein complexes involved in kinase signaling. This highly conserved gene is present in eukaryotic plants, fungi, and animals. The ortholog of this gene was first identified in plants as a key regulator of anthocyanin biosynthesis and flower pigmentation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":63550461,"end":63594266,"strand":1,"description":"DDB1 and CUL4 associated factor 7 [Source:HGNC Symbol;Acc:HGNC:30915]"}, {"versioned_ensembl_gene_id":"ENSG00000133636.10","gene_symbol":"NTS","gene_name":"neurotensin [Source:HGNC Symbol;Acc:HGNC:8038]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4922","summary":"This gene encodes a common precursor for two peptides, neuromedin N and neurotensin. Neurotensin is a secreted tridecapeptide, which is widely distributed throughout the central nervous system, and may function as a neurotransmitter or a neuromodulator. It may be involved in dopamine-associated pathophysiological events, in the maintenance of gut structure and function, and in the regulation of fat metabolism. Neurotensin also exhibits antimicrobial activity against bacteria and fungi. Tissue-specific processing may lead to the formation in some tissues of larger forms of neuromedin N and neurotensin. The large forms may represent more stable peptides that are also biologically active. [provided by RefSeq, Oct 2014]","start":85874295,"end":85882992,"strand":1,"description":"neurotensin [Source:HGNC Symbol;Acc:HGNC:8038]"}, {"versioned_ensembl_gene_id":"ENSG00000215304.3","gene_symbol":"AC135983.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32398956,"end":32435233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266256.1","gene_symbol":"LINC00683","gene_name":"long intergenic non-protein coding RNA 683 [Source:HGNC Symbol;Acc:HGNC:44467]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400660","summary":null,"start":76615212,"end":76625940,"strand":1,"description":"long intergenic non-protein coding RNA 683 [Source:HGNC Symbol;Acc:HGNC:44467]"}, {"versioned_ensembl_gene_id":"ENSG00000261802.1","gene_symbol":"AC026470.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":48447904,"end":48448398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226665.1","gene_symbol":"SSR1P2","gene_name":"signal sequence receptor subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131189","summary":null,"start":75136154,"end":75136940,"strand":1,"description":"signal sequence receptor subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39274]"}, {"versioned_ensembl_gene_id":"ENSG00000236072.1","gene_symbol":"AL592043.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34387722,"end":34388464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261936.1","gene_symbol":"TAS2R45","gene_name":"taste 2 receptor member 45 [Source:HGNC Symbol;Acc:HGNC:18876]","synonyms":"ZG24P,GPR59","biotype":"unprocessed_pseudogene","ncbi_id":"259291","summary":null,"start":11128789,"end":11129718,"strand":-1,"description":"taste 2 receptor member 45 [Source:HGNC Symbol;Acc:HGNC:18876]"}, {"versioned_ensembl_gene_id":"ENSG00000237115.2","gene_symbol":"AL139805.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131825981,"end":131828413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145945.5","gene_symbol":"FAM50B","gene_name":"family with sequence similarity 50 member B [Source:HGNC Symbol;Acc:HGNC:18789]","synonyms":"X5L,D6S2654E","biotype":"protein_coding","ncbi_id":"26240","summary":"This gene contains an intronless ORF that arose from ancestral retroposition. The encoded protein is related to a plant protein that plays a role in the circadian clock. This gene is adjacent to a differentially methylated region (DMR) and is imprinted and paternally expressed in many tissues. [provided by RefSeq, Nov 2015]","start":3849386,"end":3851317,"strand":1,"description":"family with sequence similarity 50 member B [Source:HGNC Symbol;Acc:HGNC:18789]"}, {"versioned_ensembl_gene_id":"ENSG00000249453.1","gene_symbol":"AC092834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23779590,"end":23782560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164323.12","gene_symbol":"CFAP97","gene_name":"cilia and flagella associated protein 97 [Source:HGNC Symbol;Acc:HGNC:29276]","synonyms":"KIAA1430,hmw,DKFZp434F1728","biotype":"protein_coding","ncbi_id":"57587","summary":null,"start":185159665,"end":185209504,"strand":-1,"description":"cilia and flagella associated protein 97 [Source:HGNC Symbol;Acc:HGNC:29276]"}, {"versioned_ensembl_gene_id":"ENSG00000250410.1","gene_symbol":"AC112722.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185370725,"end":185390928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011523.13","gene_symbol":"CEP68","gene_name":"centrosomal protein 68 [Source:HGNC Symbol;Acc:HGNC:29076]","synonyms":"KIAA0582","biotype":"protein_coding","ncbi_id":"23177","summary":null,"start":65056366,"end":65087004,"strand":1,"description":"centrosomal protein 68 [Source:HGNC Symbol;Acc:HGNC:29076]"}, {"versioned_ensembl_gene_id":"ENSG00000215333.3","gene_symbol":"KRT18P23","gene_name":"keratin 18 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33392]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642448","summary":null,"start":44566965,"end":44568247,"strand":1,"description":"keratin 18 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:33392]"}, {"versioned_ensembl_gene_id":"ENSG00000187012.10","gene_symbol":"LINC00207","gene_name":"long intergenic non-protein coding RNA 207 [Source:HGNC Symbol;Acc:HGNC:37255]","synonyms":"NCRNA00207","biotype":"lincRNA","ncbi_id":"388910","summary":null,"start":44569339,"end":44572341,"strand":1,"description":"long intergenic non-protein coding RNA 207 [Source:HGNC Symbol;Acc:HGNC:37255]"}, {"versioned_ensembl_gene_id":"ENSG00000259222.2","gene_symbol":"AC027088.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69080879,"end":69099987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279463.1","gene_symbol":"AL159972.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73844683,"end":73845130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164816.7","gene_symbol":"DEFA5","gene_name":"defensin alpha 5 [Source:HGNC Symbol;Acc:HGNC:2764]","synonyms":"HD-5,DEF5","biotype":"protein_coding","ncbi_id":"1670","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. Several of the alpha defensin genes appear to be clustered on chromosome 8. The protein encoded by this gene, defensin, alpha 5, is highly expressed in the secretory granules of Paneth cells of the ileum. [provided by RefSeq, Oct 2014]","start":7055304,"end":7056734,"strand":-1,"description":"defensin alpha 5 [Source:HGNC Symbol;Acc:HGNC:2764]"}, {"versioned_ensembl_gene_id":"ENSG00000197467.13","gene_symbol":"COL13A1","gene_name":"collagen type XIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2190]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1305","summary":"This gene encodes the alpha chain of one of the nonfibrillar collagens. The function of this gene product is not known, however, it has been detected at low levels in all connective tissue-producing cells so it may serve a general function in connective tissues. Unlike most of the collagens, which are secreted into the extracellular matrix, collagen XIII contains a transmembrane domain and the protein has been localized to the plasma membrane. The transcripts for this gene undergo complex and extensive splicing involving at least eight exons. Like other collagens, collagen XIII is a trimer; it is not known whether this trimer is composed of one or more than one alpha chain isomer. A number of alternatively spliced transcript variants have been described, but the full length nature of some of them has not been determined. [provided by RefSeq, Jul 2008]","start":69801931,"end":69964275,"strand":1,"description":"collagen type XIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2190]"}, {"versioned_ensembl_gene_id":"ENSG00000204296.11","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32288526,"end":32371912,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000165071.14","gene_symbol":"TMEM71","gene_name":"transmembrane protein 71 [Source:HGNC Symbol;Acc:HGNC:26572]","synonyms":"FLJ33069","biotype":"protein_coding","ncbi_id":"137835","summary":null,"start":132685007,"end":132760712,"strand":-1,"description":"transmembrane protein 71 [Source:HGNC Symbol;Acc:HGNC:26572]"}, {"versioned_ensembl_gene_id":"ENSG00000104824.16","gene_symbol":"HNRNPL","gene_name":"heterogeneous nuclear ribonucleoprotein L [Source:HGNC Symbol;Acc:HGNC:5045]","synonyms":"HNRPL","biotype":"protein_coding","ncbi_id":"3191","summary":"Heterogeneous nuclear RNAs (hnRNAs) which include mRNA precursors and mature mRNAs are associated with specific proteins to form heterogenous ribonucleoprotein (hnRNP) complexes. Heterogeneous nuclear ribonucleoprotein L is among the proteins that are stably associated with hnRNP complexes and along with other hnRNP proteins is likely to play a major role in the formation, packaging, processing, and function of mRNA. Heterogeneous nuclear ribonucleoprotein L is present in the nucleoplasm as part of the HNRP complex. HNRP proteins have also been identified outside of the nucleoplasm. Exchange of hnRNP for mRNA-binding proteins accompanies transport of mRNA from the nucleus to the cytoplasm. Since HNRP proteins have been shown to shuttle between the nucleus and the cytoplasm, it is possible that they also have cytoplasmic functions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":38836388,"end":38852347,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein L [Source:HGNC Symbol;Acc:HGNC:5045]"}, {"versioned_ensembl_gene_id":"ENSG00000266743.1","gene_symbol":"AC103808.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76173304,"end":76177738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231414.1","gene_symbol":"AC016700.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70253855,"end":70254010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229013.1","gene_symbol":"AC083939.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35471716,"end":35471841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114988.11","gene_symbol":"LMAN2L","gene_name":"lectin, mannose binding 2 like [Source:HGNC Symbol;Acc:HGNC:19263]","synonyms":"DKFZp564L2423,VIPL","biotype":"protein_coding","ncbi_id":"81562","summary":"This gene encodes a protein belonging to the L-type lectin group of type 1 membrane proteins, which function in the mammalian early secretory pathway. These proteins contain luminal carbohydrate recognition domains, which display homology to leguminous lectins. Unlike other proteins of the group, which cycle in the early secretory pathway and are predominantly associated with post endoplasmic reticulum membranes, the protein encoded by this gene is a non-cycling resident protein of the ER, where it functions as a cargo receptor for glycoproteins. It is proposed to regulate exchange of folded proteins for transport to the Golgi and exchange of misfolded glycoproteins for transport to the ubiquitin-proteasome pathway. [provided by RefSeq, Apr 2016]","start":96705929,"end":96740064,"strand":-1,"description":"lectin, mannose binding 2 like [Source:HGNC Symbol;Acc:HGNC:19263]"}, {"versioned_ensembl_gene_id":"ENSG00000268520.1","gene_symbol":"AC008750.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51361712,"end":51365544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220472.1","gene_symbol":"AL139095.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7338839,"end":7339568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110171.19","gene_symbol":"TRIM3","gene_name":"tripartite motif containing 3 [Source:HGNC Symbol;Acc:HGNC:10064]","synonyms":"RNF97,RNF22,HAC1,BERP","biotype":"protein_coding","ncbi_id":"10612","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also called the 'RING-B-box-coiled-coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic filaments. It is similar to a rat protein which is a specific partner for the tail domain of myosin V, a class of myosins which are involved in the targeted transport of organelles. The rat protein can also interact with alpha-actinin-4. Thus it is suggested that this human protein may play a role in myosin V-mediated cargo transport. Alternatively spliced transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008]","start":6448613,"end":6474459,"strand":-1,"description":"tripartite motif containing 3 [Source:HGNC Symbol;Acc:HGNC:10064]"}, {"versioned_ensembl_gene_id":"ENSG00000142549.9","gene_symbol":"IGLON5","gene_name":"IgLON family member 5 [Source:HGNC Symbol;Acc:HGNC:34550]","synonyms":"LOC402665","biotype":"protein_coding","ncbi_id":"402665","summary":null,"start":51311848,"end":51330354,"strand":1,"description":"IgLON family member 5 [Source:HGNC Symbol;Acc:HGNC:34550]"}, {"versioned_ensembl_gene_id":"ENSG00000127083.7","gene_symbol":"OMD","gene_name":"osteomodulin [Source:HGNC Symbol;Acc:HGNC:8134]","synonyms":"SLRR2C,osteoadherin","biotype":"protein_coding","ncbi_id":"4958","summary":null,"start":92414245,"end":92424461,"strand":-1,"description":"osteomodulin [Source:HGNC Symbol;Acc:HGNC:8134]"}, {"versioned_ensembl_gene_id":"ENSG00000250656.2","gene_symbol":"ST3GAL1P1","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45174]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421804","summary":null,"start":67716375,"end":67717388,"strand":-1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45174]"}, {"versioned_ensembl_gene_id":"ENSG00000104611.11","gene_symbol":"SH2D4A","gene_name":"SH2 domain containing 4A [Source:HGNC Symbol;Acc:HGNC:26102]","synonyms":"SH2A,PPP1R38,FLJ20967","biotype":"protein_coding","ncbi_id":"63898","summary":null,"start":19313617,"end":19396218,"strand":1,"description":"SH2 domain containing 4A [Source:HGNC Symbol;Acc:HGNC:26102]"}, {"versioned_ensembl_gene_id":"ENSG00000253555.1","gene_symbol":"AC011978.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63136223,"end":63138084,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228483.2","gene_symbol":"CR388415.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181532,"end":29182467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205359.9","gene_symbol":"SLCO6A1","gene_name":"solute carrier organic anion transporter family member 6A1 [Source:HGNC Symbol;Acc:HGNC:23613]","synonyms":"OATPY,OATP6A1,MGC26949,CT48","biotype":"protein_coding","ncbi_id":"133482","summary":null,"start":102371782,"end":102499016,"strand":-1,"description":"solute carrier organic anion transporter family member 6A1 [Source:HGNC Symbol;Acc:HGNC:23613]"}, {"versioned_ensembl_gene_id":"ENSG00000229885.1","gene_symbol":"AC244505.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52801400,"end":52801529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277172.1","gene_symbol":"GAPDHP41","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37798]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131935","summary":null,"start":60719222,"end":60720196,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:37798]"}, {"versioned_ensembl_gene_id":"ENSG00000103275.19","gene_symbol":"UBE2I","gene_name":"ubiquitin conjugating enzyme E2 I [Source:HGNC Symbol;Acc:HGNC:12485]","synonyms":"UBC9","biotype":"protein_coding","ncbi_id":"7329","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. Four alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":1308880,"end":1327018,"strand":1,"description":"ubiquitin conjugating enzyme E2 I [Source:HGNC Symbol;Acc:HGNC:12485]"}, {"versioned_ensembl_gene_id":"ENSG00000064651.13","gene_symbol":"SLC12A2","gene_name":"solute carrier family 12 member 2 [Source:HGNC Symbol;Acc:HGNC:10911]","synonyms":"PPP1R141,NKCC1,BSC2,BSC","biotype":"protein_coding","ncbi_id":"6558","summary":"The protein encoded by this gene mediates sodium and chloride transport and reabsorption. The encoded protein is a membrane protein and is important in maintaining proper ionic balance and cell volume. This protein is phosphorylated in response to DNA damage. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":128083766,"end":128189688,"strand":1,"description":"solute carrier family 12 member 2 [Source:HGNC Symbol;Acc:HGNC:10911]"}, {"versioned_ensembl_gene_id":"ENSG00000230485.1","gene_symbol":"AC000077.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19630750,"end":19633574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261489.1","gene_symbol":"AC025271.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57477484,"end":57478329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253280.1","gene_symbol":"AC068880.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19254241,"end":19257334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168397.16","gene_symbol":"ATG4B","gene_name":"autophagy related 4B cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:20790]","synonyms":"KIAA0943,DKFZp586D1822,AUTL1,APG4B","biotype":"protein_coding","ncbi_id":"23192","summary":"Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":241637213,"end":241673857,"strand":1,"description":"autophagy related 4B cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:20790]"}, {"versioned_ensembl_gene_id":"ENSG00000279220.1","gene_symbol":"GPR1-AS","gene_name":"GPR1 antisense RNA [Source:NCBI gene;Acc:101669764]","synonyms":"GPR1AS,GPR1-AS1","biotype":"processed_transcript","ncbi_id":"101669764","summary":"This gene is thought to produce a non-coding RNA. It is situated adjacent to a differentially methylated region (DMR) and is imprinted and paternally expressed in the placenta. [provided by RefSeq, Nov 2015]","start":206203376,"end":206266243,"strand":1,"description":"GPR1 antisense RNA [Source:NCBI gene;Acc:101669764]"}, {"versioned_ensembl_gene_id":"ENSG00000251301.6","gene_symbol":"LINC02384","gene_name":"long intergenic non-protein coding RNA 2384 [Source:HGNC Symbol;Acc:HGNC:53308]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507195","summary":null,"start":68332888,"end":68451663,"strand":-1,"description":"long intergenic non-protein coding RNA 2384 [Source:HGNC Symbol;Acc:HGNC:53308]"}, {"versioned_ensembl_gene_id":"ENSG00000246523.7","gene_symbol":"AP001528.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86955619,"end":87000959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273824.1","gene_symbol":"AC008033.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68426331,"end":68427737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250685.7","gene_symbol":"AC009123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84192558,"end":84197053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197021.8","gene_symbol":"CXorf40B","gene_name":"chromosome X open reading frame 40B [Source:HGNC Symbol;Acc:HGNC:17402]","synonyms":null,"biotype":"protein_coding","ncbi_id":"541578","summary":null,"start":149929527,"end":149938811,"strand":-1,"description":"chromosome X open reading frame 40B [Source:HGNC Symbol;Acc:HGNC:17402]"}, {"versioned_ensembl_gene_id":"ENSG00000225164.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"BAT2,G2,D6S51E","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31608127,"end":31625177,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000110195.12","gene_symbol":"FOLR1","gene_name":"folate receptor 1 [Source:HGNC Symbol;Acc:HGNC:3791]","synonyms":"FOLR","biotype":"protein_coding","ncbi_id":"2348","summary":"The protein encoded by this gene is a member of the folate receptor family. Members of this gene family bind folic acid and its reduced derivatives, and transport 5-methyltetrahydrofolate into cells. This gene product is a secreted protein that either anchors to membranes via a glycosyl-phosphatidylinositol linkage or exists in a soluble form. Mutations in this gene have been associated with neurodegeneration due to cerebral folate transport deficiency. Due to the presence of two promoters, multiple transcription start sites, and alternative splicing, multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2009]","start":72189558,"end":72196323,"strand":1,"description":"folate receptor 1 [Source:HGNC Symbol;Acc:HGNC:3791]"}, {"versioned_ensembl_gene_id":"ENSG00000216835.3","gene_symbol":"RBMXP1","gene_name":"RNA binding motif protein, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9911]","synonyms":"HNRPG,HNRNP-G","biotype":"processed_pseudogene","ncbi_id":"3186","summary":null,"start":48213604,"end":48214794,"strand":-1,"description":"RNA binding motif protein, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9911]"}, {"versioned_ensembl_gene_id":"ENSG00000265766.3","gene_symbol":"CXADRP3","gene_name":"CXADR pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33974]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"440224","summary":null,"start":14477955,"end":14499278,"strand":-1,"description":"CXADR pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33974]"}, {"versioned_ensembl_gene_id":"ENSG00000257325.1","gene_symbol":"AC138360.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100852331,"end":100859262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170423.12","gene_symbol":"KRT78","gene_name":"keratin 78 [Source:HGNC Symbol;Acc:HGNC:28926]","synonyms":"K5B","biotype":"protein_coding","ncbi_id":"196374","summary":"This gene is a member of the type II keratin gene family and encodes a protein with an intermediate filament domain. Keratins are the major structural proteins in epithelial cells, forming a cytoplasmic network of 10 to 12 nm wide intermediate filaments and creating a scaffold that gives cells the ability to withstand mechanical and non-mechanical stresses. The genes of the type II keratin family are located as a gene cluster at 12p13.13. Four pseudogenes of this gene family have been identified. [provided by RefSeq, Jul 2008]","start":52837804,"end":52849092,"strand":-1,"description":"keratin 78 [Source:HGNC Symbol;Acc:HGNC:28926]"}, {"versioned_ensembl_gene_id":"ENSG00000110079.16","gene_symbol":"MS4A4A","gene_name":"membrane spanning 4-domains A4A [Source:HGNC Symbol;Acc:HGNC:13371]","synonyms":"MS4A7,MS4A4,CD20L1","biotype":"protein_coding","ncbi_id":"51338","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features, similar intron/exon splice boundaries, and display unique expression patterns in hematopoietic cells and nonlymphoid tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":60280541,"end":60308972,"strand":1,"description":"membrane spanning 4-domains A4A [Source:HGNC Symbol;Acc:HGNC:13371]"}, {"versioned_ensembl_gene_id":"ENSG00000250254.1","gene_symbol":"PTTG2","gene_name":"pituitary tumor-transforming 2 [Source:HGNC Symbol;Acc:HGNC:9691]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10744","summary":null,"start":37960435,"end":37961125,"strand":1,"description":"pituitary tumor-transforming 2 [Source:HGNC Symbol;Acc:HGNC:9691]"}, {"versioned_ensembl_gene_id":"ENSG00000100650.15","gene_symbol":"SRSF5","gene_name":"serine and arginine rich splicing factor 5 [Source:HGNC Symbol;Acc:HGNC:10787]","synonyms":"SRP40,SFRS5,HRS","biotype":"protein_coding","ncbi_id":"6430","summary":"The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":69726900,"end":69772005,"strand":1,"description":"serine and arginine rich splicing factor 5 [Source:HGNC Symbol;Acc:HGNC:10787]"}, {"versioned_ensembl_gene_id":"ENSG00000233085.5","gene_symbol":"BX322234.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169286534,"end":169289216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203950.6","gene_symbol":"RTL8A","gene_name":"retrotransposon Gag like 8A [Source:HGNC Symbol;Acc:HGNC:24514]","synonyms":"SIRH6,MAR8A,FAM127B,DKFZP564B147,CXX1b","biotype":"protein_coding","ncbi_id":"26071","summary":null,"start":135050932,"end":135052196,"strand":-1,"description":"retrotransposon Gag like 8A [Source:HGNC Symbol;Acc:HGNC:24514]"}, {"versioned_ensembl_gene_id":"ENSG00000235065.1","gene_symbol":"RPL24P2","gene_name":"ribosomal protein L24 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16597]","synonyms":"dJ872K7.2","biotype":"processed_pseudogene","ncbi_id":"140760","summary":null,"start":21114723,"end":21115197,"strand":1,"description":"ribosomal protein L24 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16597]"}, {"versioned_ensembl_gene_id":"ENSG00000248839.1","gene_symbol":"AC021660.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98522570,"end":98525334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184867.13","gene_symbol":"ARMCX2","gene_name":"armadillo repeat containing, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:16869]","synonyms":"GASP9,ALEX2,KIAA0512","biotype":"protein_coding","ncbi_id":"9823","summary":"This gene encodes a protein containing a potential N-terminal transmembrane domain and multiple armadillo (arm) repeats. Proteins containing arm repeats are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is located in a cluster of related genes on chromosome X. There is a pseudogene for this gene on chromosome 7. Alternative splicing in the 5' UTR results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2013]","start":101655281,"end":101659891,"strand":-1,"description":"armadillo repeat containing, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:16869]"}, {"versioned_ensembl_gene_id":"ENSG00000264529.1","gene_symbol":"AC006270.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":63182166,"end":63182817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235637.1","gene_symbol":"AC069023.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17862887,"end":17865471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165695.9","gene_symbol":"AK8","gene_name":"adenylate kinase 8 [Source:HGNC Symbol;Acc:HGNC:26526]","synonyms":"FLJ32704,C9orf98","biotype":"protein_coding","ncbi_id":"158067","summary":null,"start":132725578,"end":132878777,"strand":-1,"description":"adenylate kinase 8 [Source:HGNC Symbol;Acc:HGNC:26526]"}, {"versioned_ensembl_gene_id":"ENSG00000283402.1","gene_symbol":"AC087821.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18849258,"end":18849707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265282.1","gene_symbol":"AC005828.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63430468,"end":63432211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272383.1","gene_symbol":"AC006270.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63088162,"end":63089197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052344.15","gene_symbol":"PRSS8","gene_name":"protease, serine 8 [Source:HGNC Symbol;Acc:HGNC:9491]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5652","summary":"This gene encodes a member of the peptidase S1 or chymotrypsin family of serine proteases. The encoded preproprotein is proteolytically processed to generate light and heavy chains that associate via a disulfide bond to form the heterodimeric enzyme. This enzyme is highly expressed in prostate epithelia and is one of several proteolytic enzymes found in seminal fluid. This protease exhibits trypsin-like substrate specificity, cleaving protein substrates at the carboxyl terminus of lysine or arginine residues. The encoded protease partially mediates proteolytic activation of the epithelial sodium channel, a regulator of sodium balance, and may also play a role in epithelial barrier formation. [provided by RefSeq, Feb 2016]","start":31131433,"end":31135762,"strand":-1,"description":"protease, serine 8 [Source:HGNC Symbol;Acc:HGNC:9491]"}, {"versioned_ensembl_gene_id":"ENSG00000273444.1","gene_symbol":"AC006023.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40107288,"end":40107454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206439.5","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31565793,"end":31568564,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000150510.16","gene_symbol":"FAM124A","gene_name":"family with sequence similarity 124 member A [Source:HGNC Symbol;Acc:HGNC:26413]","synonyms":"FLJ30707","biotype":"protein_coding","ncbi_id":"220108","summary":null,"start":51222334,"end":51284241,"strand":1,"description":"family with sequence similarity 124 member A [Source:HGNC Symbol;Acc:HGNC:26413]"}, {"versioned_ensembl_gene_id":"ENSG00000110077.14","gene_symbol":"MS4A6A","gene_name":"membrane spanning 4-domains A6A [Source:HGNC Symbol;Acc:HGNC:13375]","synonyms":"MS4A6,CD20L3","biotype":"protein_coding","ncbi_id":"64231","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. The gene encoding this protein is localized to 11q12.1, among a cluster of family members. Alternative splicing of this gene results in several transcript variants that encode different protein isoforms. [provided by RefSeq, Oct 2011]","start":60172014,"end":60184666,"strand":-1,"description":"membrane spanning 4-domains A6A [Source:HGNC Symbol;Acc:HGNC:13375]"}, {"versioned_ensembl_gene_id":"ENSG00000213316.9","gene_symbol":"LTC4S","gene_name":"leukotriene C4 synthase [Source:HGNC Symbol;Acc:HGNC:6719]","synonyms":"MGC33147","biotype":"protein_coding","ncbi_id":"4056","summary":"The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family includes a number of human proteins, several of which are involved the production of leukotrienes. This gene encodes an enzyme that catalyzes the first step in the biosynthesis of cysteinyl leukotrienes, potent biological compounds derived from arachidonic acid. Leukotrienes have been implicated as mediators of anaphylaxis and inflammatory conditions such as human bronchial asthma. This protein localizes to the nuclear envelope and adjacent endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":179793980,"end":179796647,"strand":1,"description":"leukotriene C4 synthase [Source:HGNC Symbol;Acc:HGNC:6719]"}, {"versioned_ensembl_gene_id":"ENSG00000272056.1","gene_symbol":"AC013472.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27053618,"end":27054276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224719.1","gene_symbol":"AC009237.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95502791,"end":95505059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237308.1","gene_symbol":"AC009237.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95496022,"end":95496531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163882.9","gene_symbol":"POLR2H","gene_name":"RNA polymerase II subunit H [Source:HGNC Symbol;Acc:HGNC:9195]","synonyms":"RPB8","biotype":"protein_coding","ncbi_id":"5437","summary":"The three eukaryotic RNA polymerases are complex multisubunit enzymes that play a central role in the transcription of nuclear genes. This gene encodes an essential and highly conserved subunit of RNA polymerase II that is shared by the other two eukaryotic DNA-directed RNA polymerases, I and III. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":184361718,"end":184368596,"strand":1,"description":"RNA polymerase II subunit H [Source:HGNC Symbol;Acc:HGNC:9195]"}, {"versioned_ensembl_gene_id":"ENSG00000270388.1","gene_symbol":"MTCO3P22","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52125]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289371","summary":null,"start":100051133,"end":100051916,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52125]"}, {"versioned_ensembl_gene_id":"ENSG00000150527.17","gene_symbol":"CTAGE5","gene_name":"CTAGE family member 5, ER export factor [Source:HGNC Symbol;Acc:HGNC:7057]","synonyms":"MGEA6,MGEA11,MGEA,MEA6,cTAGE-5D,cTAGE-5C,cTAGE-5B,cTAGE-5A","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":39230231,"end":39388513,"strand":1,"description":"CTAGE family member 5, ER export factor [Source:HGNC Symbol;Acc:HGNC:7057]"}, {"versioned_ensembl_gene_id":"ENSG00000271424.1","gene_symbol":"AL157791.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39370279,"end":39370756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253526.1","gene_symbol":"AC090802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105826570,"end":105834038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164073.10","gene_symbol":"MFSD8","gene_name":"major facilitator superfamily domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28486]","synonyms":"MGC33302,CLN7","biotype":"protein_coding","ncbi_id":"256471","summary":"This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL). [provided by RefSeq, Oct 2008]","start":127917732,"end":127966034,"strand":-1,"description":"major facilitator superfamily domain containing 8 [Source:HGNC Symbol;Acc:HGNC:28486]"}, {"versioned_ensembl_gene_id":"ENSG00000229447.2","gene_symbol":"AC114495.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31263245,"end":31263681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237293.1","gene_symbol":"AC007099.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75474453,"end":75482579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103710.10","gene_symbol":"RASL12","gene_name":"RAS like family 12 [Source:HGNC Symbol;Acc:HGNC:30289]","synonyms":"RIS","biotype":"protein_coding","ncbi_id":"51285","summary":null,"start":65053337,"end":65076690,"strand":-1,"description":"RAS like family 12 [Source:HGNC Symbol;Acc:HGNC:30289]"}, {"versioned_ensembl_gene_id":"ENSG00000143858.11","gene_symbol":"SYT2","gene_name":"synaptotagmin 2 [Source:HGNC Symbol;Acc:HGNC:11510]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127833","summary":"This gene encodes a synaptic vesicle membrane protein. The encoded protein is thought to function as a calcium sensor in vesicular trafficking and exocytosis. Mutations in this gene are associated with myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":202590596,"end":202710417,"strand":-1,"description":"synaptotagmin 2 [Source:HGNC Symbol;Acc:HGNC:11510]"}, {"versioned_ensembl_gene_id":"ENSG00000167800.9","gene_symbol":"TBX10","gene_name":"T-box 10 [Source:HGNC Symbol;Acc:HGNC:11593]","synonyms":"TBX7,TBX13","biotype":"protein_coding","ncbi_id":"347853","summary":"This gene encodes a member of the T-box family of transcription factors. These transcription factors share a DNA-binding domain called the T-box, and play a role in several developmental processes including early embryonic cell fate and organogenesis. The encoded protein is a member of the T-box 1 subfamily. Mutations in this gene are thought to be a cause of isolated cleft lip with or without cleft palate. [provided by RefSeq, Nov 2010]","start":67631303,"end":67639560,"strand":-1,"description":"T-box 10 [Source:HGNC Symbol;Acc:HGNC:11593]"}, {"versioned_ensembl_gene_id":"ENSG00000174804.3","gene_symbol":"FZD4","gene_name":"frizzled class receptor 4 [Source:HGNC Symbol;Acc:HGNC:4042]","synonyms":"EVR1,CD344","biotype":"protein_coding","ncbi_id":"8322","summary":"This gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This protein may play a role as a positive regulator of the Wingless type MMTV integration site signaling pathway. A transcript variant retaining intronic sequence and encoding a shorter isoform has been described, however, its expression is not supported by other experimental evidence. [provided by RefSeq, Jul 2008]","start":86945679,"end":86955391,"strand":-1,"description":"frizzled class receptor 4 [Source:HGNC Symbol;Acc:HGNC:4042]"}, {"versioned_ensembl_gene_id":"ENSG00000115365.11","gene_symbol":"LANCL1","gene_name":"LanC like 1 [Source:HGNC Symbol;Acc:HGNC:6508]","synonyms":"p40,GPR69A","biotype":"protein_coding","ncbi_id":"10314","summary":"This gene encodes a loosely associated peripheral membrane protein related to the LanC family of bacterial membrane-associated proteins involved in the biosynthesis of antimicrobial peptides. This protein may play a role as a peptide-modifying enzyme component in eukaryotic cells. Previously considered a member of the G-protein-coupled receptor superfamily, this protein is now in the LanC family. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2008]","start":210431249,"end":210477652,"strand":-1,"description":"LanC like 1 [Source:HGNC Symbol;Acc:HGNC:6508]"}, {"versioned_ensembl_gene_id":"ENSG00000271242.1","gene_symbol":"PRELID3BP2","gene_name":"PRELI domain containing 3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49064]","synonyms":"SLMO2P2","biotype":"processed_pseudogene","ncbi_id":"106481667","summary":null,"start":51195881,"end":51196081,"strand":1,"description":"PRELI domain containing 3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49064]"}, {"versioned_ensembl_gene_id":"ENSG00000239246.3","gene_symbol":"AC008026.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62516321,"end":62516767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269964.2","gene_symbol":"MEI4","gene_name":"meiotic double-stranded break formation protein 4 [Source:HGNC Symbol;Acc:HGNC:43638]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928601","summary":null,"start":77690658,"end":77926974,"strand":1,"description":"meiotic double-stranded break formation protein 4 [Source:HGNC Symbol;Acc:HGNC:43638]"}, {"versioned_ensembl_gene_id":"ENSG00000155858.5","gene_symbol":"LSM11","gene_name":"LSM11, U7 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:30860]","synonyms":"FLJ38273","biotype":"protein_coding","ncbi_id":"134353","summary":null,"start":157743695,"end":157760709,"strand":1,"description":"LSM11, U7 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:30860]"}, {"versioned_ensembl_gene_id":"ENSG00000274911.1","gene_symbol":"AL627230.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67725890,"end":67726544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150687.11","gene_symbol":"PRSS23","gene_name":"protease, serine 23 [Source:HGNC Symbol;Acc:HGNC:14370]","synonyms":"SPUVE,SIG13","biotype":"protein_coding","ncbi_id":"11098","summary":"This gene encodes a conserved member of the trypsin family of serine proteases. Mouse studies found a decrease of mRNA levels of this gene after ovulation was induced. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":86791059,"end":86952910,"strand":1,"description":"protease, serine 23 [Source:HGNC Symbol;Acc:HGNC:14370]"}, {"versioned_ensembl_gene_id":"ENSG00000216802.1","gene_symbol":"AL590617.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138650226,"end":138650973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276032.1","gene_symbol":"AL627230.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67723736,"end":67724105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232821.1","gene_symbol":"AC003986.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19112474,"end":19114271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215878.3","gene_symbol":"MARCKSL1P2","gene_name":"MARCKS like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45240]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100913182","summary":null,"start":138402585,"end":138403560,"strand":-1,"description":"MARCKS like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45240]"}, {"versioned_ensembl_gene_id":"ENSG00000250427.1","gene_symbol":"LINC02148","gene_name":"long intergenic non-protein coding RNA 2148 [Source:HGNC Symbol;Acc:HGNC:53008]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505811","summary":null,"start":118282575,"end":118284782,"strand":1,"description":"long intergenic non-protein coding RNA 2148 [Source:HGNC Symbol;Acc:HGNC:53008]"}, {"versioned_ensembl_gene_id":"ENSG00000249582.1","gene_symbol":"RPL7L1P4","gene_name":"ribosomal protein L7 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130968","summary":null,"start":117778826,"end":117779532,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39486]"}, {"versioned_ensembl_gene_id":"ENSG00000229190.1","gene_symbol":"AC069542.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17695709,"end":17700232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143811.18","gene_symbol":"PYCR2","gene_name":"pyrroline-5-carboxylate reductase 2 [Source:HGNC Symbol;Acc:HGNC:30262]","synonyms":"P5CR2","biotype":"protein_coding","ncbi_id":"29920","summary":"This gene belongs to the pyrroline-5-carboxylate reductase family. The encoded mitochondrial protein catalyzes the conversion of pyrroline-5-carboxylate to proline, which is the last step in proline biosynthesis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":225919877,"end":225924340,"strand":-1,"description":"pyrroline-5-carboxylate reductase 2 [Source:HGNC Symbol;Acc:HGNC:30262]"}, {"versioned_ensembl_gene_id":"ENSG00000133103.16","gene_symbol":"COG6","gene_name":"component of oligomeric golgi complex 6 [Source:HGNC Symbol;Acc:HGNC:18621]","synonyms":"KIAA1134,COD2","biotype":"protein_coding","ncbi_id":"57511","summary":"This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi apparatus. The encoded protein is organized with conserved oligomeric Golgi complex components 5, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]","start":39655627,"end":39791665,"strand":1,"description":"component of oligomeric golgi complex 6 [Source:HGNC Symbol;Acc:HGNC:18621]"}, {"versioned_ensembl_gene_id":"ENSG00000236167.1","gene_symbol":"GAPDHP57","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:38563]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421188","summary":null,"start":75455994,"end":75456578,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:38563]"}, {"versioned_ensembl_gene_id":"ENSG00000175857.8","gene_symbol":"GAPT","gene_name":"GRB2 binding adaptor protein, transmembrane [Source:HGNC Symbol;Acc:HGNC:26588]","synonyms":"FLJ33641,C5orf29","biotype":"protein_coding","ncbi_id":"202309","summary":null,"start":58491435,"end":58497090,"strand":1,"description":"GRB2 binding adaptor protein, transmembrane [Source:HGNC Symbol;Acc:HGNC:26588]"}, {"versioned_ensembl_gene_id":"ENSG00000231192.2","gene_symbol":"OR5H1","gene_name":"olfactory receptor family 5 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8346]","synonyms":"HTPCRX14,HSHTPCRX14","biotype":"protein_coding","ncbi_id":"26341","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98130721,"end":98138548,"strand":1,"description":"olfactory receptor family 5 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8346]"}, {"versioned_ensembl_gene_id":"ENSG00000213133.4","gene_symbol":"PPP1R14BP5","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:16332]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442256","summary":null,"start":126257921,"end":126258355,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:16332]"}, {"versioned_ensembl_gene_id":"ENSG00000249225.1","gene_symbol":"AC117460.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98099908,"end":98148134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255352.1","gene_symbol":"PPP1R10P1","gene_name":"protein phosphatase 1 regulatory subunit 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16325]","synonyms":"PPP1R10P","biotype":"processed_pseudogene","ncbi_id":"100422381","summary":null,"start":130789231,"end":130791025,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16325]"}, {"versioned_ensembl_gene_id":"ENSG00000175728.4","gene_symbol":"C11orf44","gene_name":"chromosome 11 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:26805]","synonyms":"FLJ39058","biotype":"lincRNA","ncbi_id":"283171","summary":null,"start":130672956,"end":130717352,"strand":1,"description":"chromosome 11 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:26805]"}, {"versioned_ensembl_gene_id":"ENSG00000250801.1","gene_symbol":"AC138965.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":175972611,"end":175985856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180549.7","gene_symbol":"FUT7","gene_name":"fucosyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4018]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2529","summary":"The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of sialyl-Lewis X antigens. The encoded protein can direct the synthesis of the E-selectin-binding sialyl-Lewis X moiety. [provided by RefSeq, Jul 2008]","start":137030174,"end":137033010,"strand":-1,"description":"fucosyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4018]"}, {"versioned_ensembl_gene_id":"ENSG00000229509.1","gene_symbol":"AC244023.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":206333327,"end":206333438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225968.7","gene_symbol":"ELFN1","gene_name":"extracellular leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33154]","synonyms":"PPP1R28","biotype":"protein_coding","ncbi_id":"392617","summary":null,"start":1688119,"end":1747954,"strand":1,"description":"extracellular leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33154]"}, {"versioned_ensembl_gene_id":"ENSG00000232880.1","gene_symbol":"NDUFB4P10","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:45258]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075105","summary":null,"start":45388347,"end":45388705,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:45258]"}, {"versioned_ensembl_gene_id":"ENSG00000257616.1","gene_symbol":"AC055716.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52730425,"end":52732865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249650.1","gene_symbol":"AC106772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":602620,"end":612210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266365.1","gene_symbol":"AC053481.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62231470,"end":62247153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266066.1","gene_symbol":"AC008158.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62136972,"end":62140639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276170.4","gene_symbol":"AC244153.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":38450394,"end":38452444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234389.1","gene_symbol":"AC007278.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":102438713,"end":102440475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213036.3","gene_symbol":"AL445305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":214482813,"end":214483387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130724.8","gene_symbol":"CHMP2A","gene_name":"charged multivesicular body protein 2A [Source:HGNC Symbol;Acc:HGNC:30216]","synonyms":"CHMP2,BC-2,VPS2A,VPS2","biotype":"protein_coding","ncbi_id":"27243","summary":"CHMP2A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":58551566,"end":58555124,"strand":-1,"description":"charged multivesicular body protein 2A [Source:HGNC Symbol;Acc:HGNC:30216]"}, {"versioned_ensembl_gene_id":"ENSG00000255001.1","gene_symbol":"AC109635.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50290749,"end":50290933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270620.1","gene_symbol":"AL034555.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15917698,"end":15917908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086102.18","gene_symbol":"NFX1","gene_name":"nuclear transcription factor, X-box binding 1 [Source:HGNC Symbol;Acc:HGNC:7803]","synonyms":"Tex42,TEG-42,NFX2,MGC20369","biotype":"protein_coding","ncbi_id":"4799","summary":"MHC class II gene expression is controlled primarily at the transcriptional level by transcription factors that bind to the X and Y boxes, two highly conserved elements in the proximal promoter of MHC class II genes. The protein encoded by this gene is a transcriptional repressor capable of binding to the conserved X box motif of HLA-DRA and other MHC class II genes in vitro. The protein may play a role in regulating the duration of an inflammatory response by limiting the period in which class II MHC molecules are induced by IFN-gamma. Three alternative splice variants, each of which encodes a different isoform, have been identified. [provided by RefSeq, Jul 2008]","start":33290511,"end":33371157,"strand":1,"description":"nuclear transcription factor, X-box binding 1 [Source:HGNC Symbol;Acc:HGNC:7803]"}, {"versioned_ensembl_gene_id":"ENSG00000148773.13","gene_symbol":"MKI67","gene_name":"marker of proliferation Ki-67 [Source:HGNC Symbol;Acc:HGNC:7107]","synonyms":"PPP1R105,MIB-","biotype":"protein_coding","ncbi_id":"4288","summary":"This gene encodes a nuclear protein that is associated with and may be necessary for cellular proliferation. Alternatively spliced transcript variants have been described. A related pseudogene exists on chromosome X. [provided by RefSeq, Mar 2009]","start":128096659,"end":128126385,"strand":-1,"description":"marker of proliferation Ki-67 [Source:HGNC Symbol;Acc:HGNC:7107]"}, {"versioned_ensembl_gene_id":"ENSG00000269588.1","gene_symbol":"AC011500.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39553034,"end":39555356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012223.12","gene_symbol":"LTF","gene_name":"lactotransferrin [Source:HGNC Symbol;Acc:HGNC:6720]","synonyms":"HLF2","biotype":"protein_coding","ncbi_id":"4057","summary":"This gene is a member of the transferrin family of genes and its protein product is found in the secondary granules of neutrophils. The protein is a major iron-binding protein in milk and body secretions with an antimicrobial activity, making it an important component of the non-specific immune system. The protein demonstrates a broad spectrum of properties, including regulation of iron homeostasis, host defense against a broad range of microbial infections, anti-inflammatory activity, regulation of cellular growth and differentiation and protection against cancer development and metastasis. Antimicrobial, antiviral, antifungal and antiparasitic activity has been found for this protein and its peptides. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":46435645,"end":46485234,"strand":-1,"description":"lactotransferrin [Source:HGNC Symbol;Acc:HGNC:6720]"}, {"versioned_ensembl_gene_id":"ENSG00000250428.1","gene_symbol":"AC100858.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124920428,"end":124922076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140015.19","gene_symbol":"KCNH5","gene_name":"potassium voltage-gated channel subfamily H member 5 [Source:HGNC Symbol;Acc:HGNC:6254]","synonyms":"Kv10.2,H-EAG2,eag2","biotype":"protein_coding","ncbi_id":"27133","summary":"This gene encodes a member of voltage-gated potassium channels. Members of this family have diverse functions, including regulating neurotransmitter and hormone release, cardiac function, and cell volume. This protein is an outward-rectifying, noninactivating channel. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":62699454,"end":63102037,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 5 [Source:HGNC Symbol;Acc:HGNC:6254]"}, {"versioned_ensembl_gene_id":"ENSG00000149507.6","gene_symbol":"OOSP2","gene_name":"oocyte secreted protein 2 [Source:HGNC Symbol;Acc:HGNC:26699]","synonyms":"FLJ36198,TMEM122,PLAC1L","biotype":"protein_coding","ncbi_id":"219990","summary":null,"start":60040275,"end":60048044,"strand":1,"description":"oocyte secreted protein 2 [Source:HGNC Symbol;Acc:HGNC:26699]"}, {"versioned_ensembl_gene_id":"ENSG00000270852.1","gene_symbol":"AL390816.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62150656,"end":62152258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112562.18","gene_symbol":"SMOC2","gene_name":"SPARC related modular calcium binding 2 [Source:HGNC Symbol;Acc:HGNC:20323]","synonyms":"SMAP2","biotype":"protein_coding","ncbi_id":"64094","summary":"This gene encodes a member of the SPARC family (secreted protein acidic and rich in cysteine/osteonectin/BM-40), which are highly expressed during embryogenesis and wound healing. The gene product is a matricellular protein which promotes matrix assembly and can stimulate endothelial cell proliferation and migration, as well as angiogenic activity. Associated with pulmonary function, this secretory gene product contains a Kazal domain, two thymoglobulin type-1 domains, and two EF-hand calcium-binding domains. The encoded protein may serve as a target for controlling angiogenesis in tumor growth and myocardial ischemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":168441151,"end":168673445,"strand":1,"description":"SPARC related modular calcium binding 2 [Source:HGNC Symbol;Acc:HGNC:20323]"}, {"versioned_ensembl_gene_id":"ENSG00000249500.1","gene_symbol":"LINC01179","gene_name":"long intergenic non-protein coding RNA 1179 [Source:HGNC Symbol;Acc:HGNC:49556]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928151","summary":null,"start":165684639,"end":165762778,"strand":1,"description":"long intergenic non-protein coding RNA 1179 [Source:HGNC Symbol;Acc:HGNC:49556]"}, {"versioned_ensembl_gene_id":"ENSG00000186838.13","gene_symbol":"SELENOV","gene_name":"selenoprotein V [Source:HGNC Symbol;Acc:HGNC:30399]","synonyms":"SELV","biotype":"protein_coding","ncbi_id":"348303","summary":"This gene encodes a selenoprotein containing a selenocysteine (Sec) residue, which is encoded by the UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is specifically expressed in the testis. It belongs to the SelWTH family, which possesses a thioredoxin-like fold and a conserved CxxU (C is cysteine, U is Sec) motif, suggesting a redox function for this gene. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Apr 2017]","start":39515113,"end":39520686,"strand":1,"description":"selenoprotein V [Source:HGNC Symbol;Acc:HGNC:30399]"}, {"versioned_ensembl_gene_id":"ENSG00000248327.1","gene_symbol":"NOL8P1","gene_name":"nucleolar protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402191","summary":null,"start":165547532,"end":165551060,"strand":-1,"description":"nucleolar protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49557]"}, {"versioned_ensembl_gene_id":"ENSG00000067955.13","gene_symbol":"CBFB","gene_name":"core-binding factor beta subunit [Source:HGNC Symbol;Acc:HGNC:1539]","synonyms":"PEBP2B","biotype":"protein_coding","ncbi_id":"865","summary":"The protein encoded by this gene is the beta subunit of a heterodimeric core-binding transcription factor belonging to the PEBP2/CBF transcription factor family which master-regulates a host of genes specific to hematopoiesis (e.g., RUNX1) and osteogenesis (e.g., RUNX2). The beta subunit is a non-DNA binding regulatory subunit; it allosterically enhances DNA binding by alpha subunit as the complex binds to the core site of various enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers and GM-CSF promoters. Alternative splicing generates two mRNA variants, each encoding a distinct carboxyl terminus. In some cases, a pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript consisting of the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain 11. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":67029116,"end":67101058,"strand":1,"description":"core-binding factor beta subunit [Source:HGNC Symbol;Acc:HGNC:1539]"}, {"versioned_ensembl_gene_id":"ENSG00000261338.2","gene_symbol":"AC021016.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":218255319,"end":218257366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238012.1","gene_symbol":"AC114752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64330486,"end":64332131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215900.4","gene_symbol":"SELENOWP1","gene_name":"selenoprotein W pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10753]","synonyms":"SEPW1P","biotype":"processed_pseudogene","ncbi_id":"23679","summary":null,"start":31094987,"end":31095558,"strand":-1,"description":"selenoprotein W pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10753]"}, {"versioned_ensembl_gene_id":"ENSG00000227076.1","gene_symbol":"AL158166.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":127934698,"end":127936167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103647.12","gene_symbol":"CORO2B","gene_name":"coronin 2B [Source:HGNC Symbol;Acc:HGNC:2256]","synonyms":"KIAA0925,ClipinC","biotype":"protein_coding","ncbi_id":"10391","summary":null,"start":68578969,"end":68727806,"strand":1,"description":"coronin 2B [Source:HGNC Symbol;Acc:HGNC:2256]"}, {"versioned_ensembl_gene_id":"ENSG00000175764.14","gene_symbol":"TTLL11","gene_name":"tubulin tyrosine ligase like 11 [Source:HGNC Symbol;Acc:HGNC:18113]","synonyms":"C9orf20,bA244O19.1","biotype":"protein_coding","ncbi_id":"158135","summary":null,"start":121821928,"end":122093606,"strand":-1,"description":"tubulin tyrosine ligase like 11 [Source:HGNC Symbol;Acc:HGNC:18113]"}, {"versioned_ensembl_gene_id":"ENSG00000279379.1","gene_symbol":"AC024595.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19257951,"end":19258337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249441.1","gene_symbol":"AC110767.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19747179,"end":19754591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184845.3","gene_symbol":"DRD1","gene_name":"dopamine receptor D1 [Source:HGNC Symbol;Acc:HGNC:3020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1812","summary":"This gene encodes the D1 subtype of the dopamine receptor. The D1 subtype is the most abundant dopamine receptor in the central nervous system. This G-protein coupled receptor stimulates adenylyl cyclase and activates cyclic AMP-dependent protein kinases. D1 receptors regulate neuronal growth and development, mediate some behavioral responses, and modulate dopamine receptor D2-mediated events. Alternate transcription initiation sites result in two transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":175440039,"end":175444208,"strand":-1,"description":"dopamine receptor D1 [Source:HGNC Symbol;Acc:HGNC:3020]"}, {"versioned_ensembl_gene_id":"ENSG00000248355.1","gene_symbol":"ARL2BPP6","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874421","summary":null,"start":175290731,"end":175291252,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39450]"}, {"versioned_ensembl_gene_id":"ENSG00000163389.10","gene_symbol":"POGLUT1","gene_name":"protein O-glucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:22954]","synonyms":"MDSRP,MDS010,KTELC1,KDELCL1,hCLP46,C3orf9,9630046K23Rik,Rumi,MGC32995","biotype":"protein_coding","ncbi_id":"56983","summary":"This gene encodes a protein with both O-glucosyltransferase and O-xylosyltransferase activity which localizes to the lumen of the endoplasmic reticulum. This protein has a carboxy-terminal KTEL motif which is predicted to function as an endoplasmic reticulum retention signal. This gene is an essential regulator of Notch signalling and likely plays a role in cell fate and tissue formation during development. It may also play a role in the pathogenesis of leukemia. Mutations in this gene have been associated with the autosomal dominant genodermatosis Dowling-Degos disease 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":119468938,"end":119494708,"strand":1,"description":"protein O-glucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:22954]"}, {"versioned_ensembl_gene_id":"ENSG00000111404.6","gene_symbol":"RERGL","gene_name":"RERG like [Source:HGNC Symbol;Acc:HGNC:26213]","synonyms":"FLJ22655","biotype":"protein_coding","ncbi_id":"79785","summary":null,"start":18080869,"end":18320107,"strand":-1,"description":"RERG like [Source:HGNC Symbol;Acc:HGNC:26213]"}, {"versioned_ensembl_gene_id":"ENSG00000089327.14","gene_symbol":"FXYD5","gene_name":"FXYD domain containing ion transport regulator 5 [Source:HGNC Symbol;Acc:HGNC:4029]","synonyms":"OIT2","biotype":"protein_coding","ncbi_id":"53827","summary":"This gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD-domain containing ion transport regulator. Mouse FXYD5 has been termed RIC (Related to Ion Channel). FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. Transmembrane topology has been established for two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. This gene product, FXYD5, is a glycoprotein that functions in the up-regulation of chemokine production, and it is involved in the reduction of cell adhesion via its ability to down-regulate E-cadherin. It also promotes metastasis, and has been linked to a variety of cancers. Alternative splicing results in multiple transcript variants. [RefSeq curation by Kathleen J. Sweadner, Ph.D., sweadner@helix.mgh.harvard.edu., Sep 2009]","start":35154730,"end":35169883,"strand":1,"description":"FXYD domain containing ion transport regulator 5 [Source:HGNC Symbol;Acc:HGNC:4029]"}, {"versioned_ensembl_gene_id":"ENSG00000134256.12","gene_symbol":"CD101","gene_name":"CD101 molecule [Source:HGNC Symbol;Acc:HGNC:5949]","synonyms":"V7,IGSF2","biotype":"protein_coding","ncbi_id":"9398","summary":null,"start":117001750,"end":117036476,"strand":1,"description":"CD101 molecule [Source:HGNC Symbol;Acc:HGNC:5949]"}, {"versioned_ensembl_gene_id":"ENSG00000100926.14","gene_symbol":"TM9SF1","gene_name":"transmembrane 9 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11864]","synonyms":"MP70,HMP70","biotype":"protein_coding","ncbi_id":"10548","summary":null,"start":24189143,"end":24195687,"strand":-1,"description":"transmembrane 9 superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:11864]"}, {"versioned_ensembl_gene_id":"ENSG00000282238.1","gene_symbol":"RPS26P8","gene_name":"ribosomal protein S26 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644191","summary":null,"start":45620204,"end":45620551,"strand":1,"description":"ribosomal protein S26 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31329]"}, {"versioned_ensembl_gene_id":"ENSG00000148229.12","gene_symbol":"POLE3","gene_name":"DNA polymerase epsilon 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:13546]","synonyms":"Ybl1,p17,CHRAC17,CHARAC17","biotype":"protein_coding","ncbi_id":"54107","summary":"POLE3 is a histone-fold protein that interacts with other histone-fold proteins to bind DNA in a sequence-independent manner. These histone-fold protein dimers combine within larger enzymatic complexes for DNA transcription, replication, and packaging.[supplied by OMIM, Apr 2004]","start":113407235,"end":113410672,"strand":-1,"description":"DNA polymerase epsilon 3, accessory subunit [Source:HGNC Symbol;Acc:HGNC:13546]"}, {"versioned_ensembl_gene_id":"ENSG00000237278.2","gene_symbol":"RLIMP2","gene_name":"ring finger protein, LIM domain interacting pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39683]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533731","summary":null,"start":113125321,"end":113126883,"strand":-1,"description":"ring finger protein, LIM domain interacting pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39683]"}, {"versioned_ensembl_gene_id":"ENSG00000282727.1","gene_symbol":"AC244207.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45543212,"end":45545473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275710.1","gene_symbol":"AC007485.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54964474,"end":54964679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164822.4","gene_symbol":"DEFA6","gene_name":"defensin alpha 6 [Source:HGNC Symbol;Acc:HGNC:2765]","synonyms":"DEF6,HD-6","biotype":"protein_coding","ncbi_id":"1671","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. Several alpha defensin genes appear to be clustered on chromosome 8. The protein encoded by this gene, defensin, alpha 6, is highly expressed in the secretory granules of Paneth cells of the small intestine, and likely plays a role in host defense of human bowel. [provided by RefSeq, Oct 2014]","start":6924693,"end":6926076,"strand":-1,"description":"defensin alpha 6 [Source:HGNC Symbol;Acc:HGNC:2765]"}, {"versioned_ensembl_gene_id":"ENSG00000134827.7","gene_symbol":"TCN1","gene_name":"transcobalamin 1 [Source:HGNC Symbol;Acc:HGNC:11652]","synonyms":"TCI,TC1","biotype":"protein_coding","ncbi_id":"6947","summary":"This gene encodes a member of the vitamin B12-binding protein family. This family of proteins, alternatively referred to as R binders, is expressed in various tissues and secretions. This protein is a major constituent of secondary granules in neutrophils and facilitates the transport of cobalamin into cells. [provided by RefSeq, Jul 2008]","start":59852800,"end":59866575,"strand":-1,"description":"transcobalamin 1 [Source:HGNC Symbol;Acc:HGNC:11652]"}, {"versioned_ensembl_gene_id":"ENSG00000131653.12","gene_symbol":"TRAF7","gene_name":"TNF receptor associated factor 7 [Source:HGNC Symbol;Acc:HGNC:20456]","synonyms":"RNF119,RFWD1,MGC7807,DKFZp586I021","biotype":"protein_coding","ncbi_id":"84231","summary":"Tumor necrosis factor (TNF; see MIM 191160) receptor-associated factors, such as TRAF7, are signal transducers for members of the TNF receptor superfamily (see MIM 191190). TRAFs are composed of an N-terminal cysteine/histidine-rich region containing zinc RING and/or zinc finger motifs; a coiled-coil (leucine zipper) motif; and a homologous region that defines the TRAF family, the TRAF domain, which is involved in self-association and receptor binding.[supplied by OMIM, Apr 2004]","start":2155698,"end":2178129,"strand":1,"description":"TNF receptor associated factor 7 [Source:HGNC Symbol;Acc:HGNC:20456]"}, {"versioned_ensembl_gene_id":"ENSG00000121075.9","gene_symbol":"TBX4","gene_name":"T-box 4 [Source:HGNC Symbol;Acc:HGNC:11603]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9496","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is the human homolog of mouse Tbx4, which is closely linked to Tbx2 on mouse chromosome 11. Similarly this gene, like TBX2, maps to human chromosome 17. Expression studies in mouse and chicken show that Tbx4 is expressed in developing hindlimb, but not in forelimb buds, suggesting a role for this gene in regulating limb development and specification of limb identity. [provided by RefSeq, Jul 2008]","start":61452404,"end":61485110,"strand":1,"description":"T-box 4 [Source:HGNC Symbol;Acc:HGNC:11603]"}, {"versioned_ensembl_gene_id":"ENSG00000151726.13","gene_symbol":"ACSL1","gene_name":"acyl-CoA synthetase long chain family member 1 [Source:HGNC Symbol;Acc:HGNC:3569]","synonyms":"LACS,FACL2,FACL1,ACS1,LACS2,LACS1","biotype":"protein_coding","ncbi_id":"2180","summary":"The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":184755595,"end":184826818,"strand":-1,"description":"acyl-CoA synthetase long chain family member 1 [Source:HGNC Symbol;Acc:HGNC:3569]"}, {"versioned_ensembl_gene_id":"ENSG00000239665.8","gene_symbol":"AL157392.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":13631143,"end":13668445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254408.1","gene_symbol":"OR4A1P","gene_name":"olfactory receptor family 4 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8289]","synonyms":"OR4A20P,OR11-30","biotype":"unprocessed_pseudogene","ncbi_id":"8596","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49898267,"end":49899186,"strand":-1,"description":"olfactory receptor family 4 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8289]"}, {"versioned_ensembl_gene_id":"ENSG00000233169.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31697782,"end":31700175,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000234647.2","gene_symbol":"AL606970.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168242938,"end":168262581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215227.4","gene_symbol":"NUTF2P5","gene_name":"nuclear transport factor 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481706","summary":null,"start":13870797,"end":13871175,"strand":1,"description":"nuclear transport factor 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50454]"}, {"versioned_ensembl_gene_id":"ENSG00000249138.1","gene_symbol":"SLED1","gene_name":"proteoglycan 3 pseudogene [Source:NCBI gene;Acc:643036]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"643036","summary":null,"start":184798296,"end":184799046,"strand":-1,"description":"proteoglycan 3 pseudogene [Source:NCBI gene;Acc:643036]"}, {"versioned_ensembl_gene_id":"ENSG00000266962.2","gene_symbol":"AC067852.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42552436,"end":42554748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231770.5","gene_symbol":"TMEM44-AS1","gene_name":"TMEM44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44272]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507297","summary":null,"start":194584011,"end":194590260,"strand":1,"description":"TMEM44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44272]"}, {"versioned_ensembl_gene_id":"ENSG00000279999.1","gene_symbol":"AL353997.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18424321,"end":18425097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259108.2","gene_symbol":"LINC01595","gene_name":"long intergenic non-protein coding RNA 1595 [Source:HGNC Symbol;Acc:HGNC:51586]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102725176","summary":null,"start":47863483,"end":47865341,"strand":-1,"description":"long intergenic non-protein coding RNA 1595 [Source:HGNC Symbol;Acc:HGNC:51586]"}, {"versioned_ensembl_gene_id":"ENSG00000274487.1","gene_symbol":"AC244154.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38195740,"end":38257152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259009.4","gene_symbol":"TPRX2P","gene_name":"tetrapeptide repeat homeobox 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32175]","synonyms":"TPRX2P1","biotype":"unprocessed_pseudogene","ncbi_id":"503627","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the TPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":47860113,"end":47861512,"strand":1,"description":"tetrapeptide repeat homeobox 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32175]"}, {"versioned_ensembl_gene_id":"ENSG00000279505.1","gene_symbol":"AC022513.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67753701,"end":67753817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270118.1","gene_symbol":"AC138894.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28454141,"end":28454511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276188.1","gene_symbol":"AC069234.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120709112,"end":120709523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143341.11","gene_symbol":"HMCN1","gene_name":"hemicentin 1 [Source:HGNC Symbol;Acc:HGNC:19194]","synonyms":"FIBL6,FIBL-6,FBLN6,ARMD1","biotype":"protein_coding","ncbi_id":"83872","summary":"This gene encodes a large extracellular member of the immunoglobulin superfamily. A similar protein in C. elegans forms long, fine tracks at specific extracellular sites that are involved in many processes such as stabilization of the germline syncytium, anchorage of mechanosensory neurons to the epidermis, and organization of hemidesmosomes in the epidermis. Mutations in this gene may be associated with age-related macular degeneration. [provided by RefSeq, Jul 2008]","start":185734551,"end":186190949,"strand":1,"description":"hemicentin 1 [Source:HGNC Symbol;Acc:HGNC:19194]"}, {"versioned_ensembl_gene_id":"ENSG00000227665.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31640507,"end":31642899,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000225483.1","gene_symbol":"AC244035.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206160887,"end":206161276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205609.12","gene_symbol":"EIF3CL","gene_name":"eukaryotic translation initiation factor 3 subunit C like [Source:HGNC Symbol;Acc:HGNC:26347]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728689","summary":"The protein encoded by this gene is a core subunit of the eukaryotic translation initiation factor 3 (eIF3) complex. The encoded protein is nearly identical to another protein, eIF3c, from a related gene. The eIF3 complex binds the 40S ribosome and mRNAs to enable translation initiation. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015]","start":28379579,"end":28403879,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit C like [Source:HGNC Symbol;Acc:HGNC:26347]"}, {"versioned_ensembl_gene_id":"ENSG00000263961.6","gene_symbol":"C1orf186","gene_name":"chromosome 1 open reading frame 186 [Source:HGNC Symbol;Acc:HGNC:25341]","synonyms":"FLJ16052","biotype":"protein_coding","ncbi_id":"440712","summary":null,"start":206037231,"end":206102459,"strand":1,"description":"chromosome 1 open reading frame 186 [Source:HGNC Symbol;Acc:HGNC:25341]"}, {"versioned_ensembl_gene_id":"ENSG00000251045.1","gene_symbol":"LINC01959","gene_name":"long intergenic non-protein coding RNA 1959 [Source:HGNC Symbol;Acc:HGNC:27965]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340074","summary":null,"start":135648584,"end":135653935,"strand":-1,"description":"long intergenic non-protein coding RNA 1959 [Source:HGNC Symbol;Acc:HGNC:27965]"}, {"versioned_ensembl_gene_id":"ENSG00000246174.7","gene_symbol":"KCTD21-AS1","gene_name":"KCTD21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48674]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289388","summary":null,"start":78139771,"end":78175323,"strand":1,"description":"KCTD21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48674]"}, {"versioned_ensembl_gene_id":"ENSG00000269271.1","gene_symbol":"AC245036.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54589441,"end":54590287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261077.1","gene_symbol":"AC016180.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86139838,"end":86140240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170091.10","gene_symbol":"HGNC:24955","gene_name":"Neuron-specific protein family member 2 [Source:UniProtKB/Swiss-Prot;Acc:Q9Y328]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":174045604,"end":174243501,"strand":1,"description":"Neuron-specific protein family member 2 [Source:UniProtKB/Swiss-Prot;Acc:Q9Y328]"}, {"versioned_ensembl_gene_id":"ENSG00000115998.7","gene_symbol":"C2orf42","gene_name":"chromosome 2 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:26056]","synonyms":"FLJ20558","biotype":"protein_coding","ncbi_id":"54980","summary":null,"start":70149880,"end":70248615,"strand":-1,"description":"chromosome 2 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:26056]"}, {"versioned_ensembl_gene_id":"ENSG00000154305.16","gene_symbol":"MIA3","gene_name":"MIA family member 3, ER export factor [Source:HGNC Symbol;Acc:HGNC:24008]","synonyms":"UNQ6077,TANGO1,TANGO,KIAA0268,FLJ39207","biotype":"protein_coding","ncbi_id":"375056","summary":null,"start":222618086,"end":222668012,"strand":1,"description":"MIA family member 3, ER export factor [Source:HGNC Symbol;Acc:HGNC:24008]"}, {"versioned_ensembl_gene_id":"ENSG00000108342.12","gene_symbol":"CSF3","gene_name":"colony stimulating factor 3 [Source:HGNC Symbol;Acc:HGNC:2438]","synonyms":"GCSF,G-CSF,C17orf33,MGC45931","biotype":"protein_coding","ncbi_id":"1440","summary":"This gene encodes a member of the IL-6 superfamily of cytokines. The encoded cytokine controls the production, differentiation, and function of granulocytes. Granulocytes are a type of white blood cell that are part of the innate immune response. A modified form of this protein is commonly administered to manage chemotherapy-induced neutropenia. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2020]","start":40015361,"end":40017813,"strand":1,"description":"colony stimulating factor 3 [Source:HGNC Symbol;Acc:HGNC:2438]"}, {"versioned_ensembl_gene_id":"ENSG00000164038.14","gene_symbol":"SLC9B2","gene_name":"solute carrier family 9 member B2 [Source:HGNC Symbol;Acc:HGNC:25143]","synonyms":"NHEDC2,NHA2,FLJ23984","biotype":"protein_coding","ncbi_id":"133308","summary":"Sodium hydrogen antiporters, such as NHEDC2, convert the proton motive force established by the respiratory chain or the F1F0 mitochondrial ATPase into sodium gradients that drive other energy-requiring processes, transduce environmental signals into cell responses, or function in drug efflux (Xiang et al., 2007 [PubMed 18000046]).[supplied by OMIM, Mar 2008]","start":103019868,"end":103085829,"strand":-1,"description":"solute carrier family 9 member B2 [Source:HGNC Symbol;Acc:HGNC:25143]"}, {"versioned_ensembl_gene_id":"ENSG00000183864.4","gene_symbol":"TOB2","gene_name":"transducer of ERBB2, 2 [Source:HGNC Symbol;Acc:HGNC:11980]","synonyms":"APRO5,TROB2,TOBL,TOB4,bK223H9","biotype":"protein_coding","ncbi_id":"10766","summary":"TOB2 belongs to the TOB (see TOB1; MIM 605523)/BTG1 (MIM 109580) family of antiproliferative proteins, which are involved in the regulation of cell cycle progression.[supplied by OMIM, Apr 2004]","start":41433492,"end":41447023,"strand":-1,"description":"transducer of ERBB2, 2 [Source:HGNC Symbol;Acc:HGNC:11980]"}, {"versioned_ensembl_gene_id":"ENSG00000171206.13","gene_symbol":"TRIM8","gene_name":"tripartite motif containing 8 [Source:HGNC Symbol;Acc:HGNC:15579]","synonyms":"RNF27,GERP","biotype":"protein_coding","ncbi_id":"81603","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. Based on similarities to other proteins, the encoded protein is suspected to be an E3 ubiquitin-protein ligase. Regulation of this gene may be altered in some cancers. Mutations resulting in a truncated protein product have been observed in early-onset epileptic encephalopathy (EOEE). [provided by RefSeq, Sep 2016]","start":102644496,"end":102658407,"strand":1,"description":"tripartite motif containing 8 [Source:HGNC Symbol;Acc:HGNC:15579]"}, {"versioned_ensembl_gene_id":"ENSG00000184857.7","gene_symbol":"TMEM186","gene_name":"transmembrane protein 186 [Source:HGNC Symbol;Acc:HGNC:24530]","synonyms":"DKFZP564K2062,C16orf51","biotype":"protein_coding","ncbi_id":"25880","summary":"This gene encodes a potential transmembrane protein. [provided by RefSeq, Dec 2012]","start":8780384,"end":8797648,"strand":-1,"description":"transmembrane protein 186 [Source:HGNC Symbol;Acc:HGNC:24530]"}, {"versioned_ensembl_gene_id":"ENSG00000103061.12","gene_symbol":"SLC7A6OS","gene_name":"solute carrier family 7 member 6 opposite strand [Source:HGNC Symbol;Acc:HGNC:25807]","synonyms":"FLJ13291","biotype":"protein_coding","ncbi_id":"84138","summary":null,"start":68284503,"end":68310946,"strand":-1,"description":"solute carrier family 7 member 6 opposite strand [Source:HGNC Symbol;Acc:HGNC:25807]"}, {"versioned_ensembl_gene_id":"ENSG00000254783.1","gene_symbol":"AP003084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86283927,"end":86284668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251588.2","gene_symbol":"AC125336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36506043,"end":36508869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256028.2","gene_symbol":"AC026362.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":122975320,"end":122982907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141200.7","gene_symbol":"KIF2B","gene_name":"kinesin family member 2B [Source:HGNC Symbol;Acc:HGNC:29443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84643","summary":null,"start":53822901,"end":53825213,"strand":1,"description":"kinesin family member 2B [Source:HGNC Symbol;Acc:HGNC:29443]"}, {"versioned_ensembl_gene_id":"ENSG00000198454.2","gene_symbol":"PRR31","gene_name":"proline rich 31 [Source:HGNC Symbol;Acc:HGNC:18147]","synonyms":"C9orf141","biotype":"lincRNA","ncbi_id":"101928638","summary":null,"start":136969243,"end":136971990,"strand":1,"description":"proline rich 31 [Source:HGNC Symbol;Acc:HGNC:18147]"}, {"versioned_ensembl_gene_id":"ENSG00000154127.9","gene_symbol":"UBASH3B","gene_name":"ubiquitin associated and SH3 domain containing B [Source:HGNC Symbol;Acc:HGNC:29884]","synonyms":"TULA2,TULA-2,STS-1,KIAA1959","biotype":"protein_coding","ncbi_id":"84959","summary":"This gene encodes a protein that contains a ubiquitin associated domain at the N-terminus, an SH3 domain, and a C-terminal domain with similarities to the catalytic motif of phosphoglycerate mutase. The encoded protein was found to inhibit endocytosis of epidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor. [provided by RefSeq, Jul 2008]","start":122655675,"end":122814473,"strand":1,"description":"ubiquitin associated and SH3 domain containing B [Source:HGNC Symbol;Acc:HGNC:29884]"}, {"versioned_ensembl_gene_id":"ENSG00000186265.9","gene_symbol":"BTLA","gene_name":"B and T lymphocyte associated [Source:HGNC Symbol;Acc:HGNC:21087]","synonyms":"CD272,BTLA1","biotype":"protein_coding","ncbi_id":"151888","summary":"This gene encodes a member of the immunoglobulin superfamily. The encoded protein contains a single immunoglobulin (Ig) domain and is a receptor that relays inhibitory signals to suppress the immune response. Alternative splicing results in multiple transcript variants. Polymorphisms in this gene have been associated with an increased risk of rheumatoid arthritis. [provided by RefSeq, Aug 2011]","start":112463968,"end":112499561,"strand":-1,"description":"B and T lymphocyte associated [Source:HGNC Symbol;Acc:HGNC:21087]"}, {"versioned_ensembl_gene_id":"ENSG00000178772.6","gene_symbol":"CPN2","gene_name":"carboxypeptidase N subunit 2 [Source:HGNC Symbol;Acc:HGNC:2313]","synonyms":"ACBP","biotype":"protein_coding","ncbi_id":"1370","summary":null,"start":194339765,"end":194351328,"strand":-1,"description":"carboxypeptidase N subunit 2 [Source:HGNC Symbol;Acc:HGNC:2313]"}, {"versioned_ensembl_gene_id":"ENSG00000234284.6","gene_symbol":"ZNF879","gene_name":"zinc finger protein 879 [Source:HGNC Symbol;Acc:HGNC:37273]","synonyms":"DKFZp686E2433","biotype":"protein_coding","ncbi_id":"345462","summary":"This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and thirteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017]","start":179023752,"end":179035064,"strand":1,"description":"zinc finger protein 879 [Source:HGNC Symbol;Acc:HGNC:37273]"}, {"versioned_ensembl_gene_id":"ENSG00000214544.7","gene_symbol":"GTF2IRD2P1","gene_name":"GTF2I repeat domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33127]","synonyms":"GTF2IRD2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401375","summary":null,"start":73242751,"end":73280119,"strand":-1,"description":"GTF2I repeat domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33127]"}, {"versioned_ensembl_gene_id":"ENSG00000283240.1","gene_symbol":"AC007529.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16661766,"end":16788375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235528.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33245863,"end":33251405,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000149582.15","gene_symbol":"TMEM25","gene_name":"transmembrane protein 25 [Source:HGNC Symbol;Acc:HGNC:25890]","synonyms":"FLJ14399","biotype":"protein_coding","ncbi_id":"84866","summary":null,"start":118531041,"end":118547280,"strand":1,"description":"transmembrane protein 25 [Source:HGNC Symbol;Acc:HGNC:25890]"}, {"versioned_ensembl_gene_id":"ENSG00000178187.7","gene_symbol":"ZNF454","gene_name":"zinc finger protein 454 [Source:HGNC Symbol;Acc:HGNC:21200]","synonyms":"FLJ37444","biotype":"protein_coding","ncbi_id":"285676","summary":null,"start":178941191,"end":178966433,"strand":1,"description":"zinc finger protein 454 [Source:HGNC Symbol;Acc:HGNC:21200]"}, {"versioned_ensembl_gene_id":"ENSG00000213735.2","gene_symbol":"ANAPC10P1","gene_name":"anaphase promoting complex subunit 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33976]","synonyms":"ANAPC10P","biotype":"processed_pseudogene","ncbi_id":"729198","summary":null,"start":52253621,"end":52254176,"strand":1,"description":"anaphase promoting complex subunit 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33976]"}, {"versioned_ensembl_gene_id":"ENSG00000224255.2","gene_symbol":"PDCL3P6","gene_name":"phosducin-like 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44507]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419023","summary":null,"start":52179848,"end":52180553,"strand":1,"description":"phosducin-like 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44507]"}, {"versioned_ensembl_gene_id":"ENSG00000272100.1","gene_symbol":"AL513218.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52353487,"end":52353877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188517.14","gene_symbol":"COL25A1","gene_name":"collagen type XXV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:18603]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84570","summary":"This gene encodes a brain-specific membrane associated collagen. A product of proteolytic processing of the encoded protein, CLAC (collagenous Alzheimer amyloid plaque component), binds to amyloid beta-peptides found in Alzheimer amyloid plaques but CLAC inhibits rather than facilitates amyloid fibril elongation (PMID: 16300410). A study of over-expression of this collagen in mice, however, found changes in pathology and behavior suggesting that the encoded protein may promote amyloid plaque formation (PMID: 19548013). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":108810721,"end":109302657,"strand":-1,"description":"collagen type XXV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:18603]"}, {"versioned_ensembl_gene_id":"ENSG00000225086.1","gene_symbol":"BX927229.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30001259,"end":30002254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272721.5","gene_symbol":"AC131235.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":184134019,"end":184135238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109205.16","gene_symbol":"ODAM","gene_name":"odontogenic, ameloblast asssociated [Source:HGNC Symbol;Acc:HGNC:26043]","synonyms":"FLJ20513,APin","biotype":"protein_coding","ncbi_id":"54959","summary":null,"start":70196496,"end":70204576,"strand":1,"description":"odontogenic, ameloblast asssociated [Source:HGNC Symbol;Acc:HGNC:26043]"}, {"versioned_ensembl_gene_id":"ENSG00000172115.8","gene_symbol":"CYCS","gene_name":"cytochrome c, somatic [Source:HGNC Symbol;Acc:HGNC:19986]","synonyms":"HCS,CYC","biotype":"protein_coding","ncbi_id":"54205","summary":"This gene encodes a small heme protein that functions as a central component of the electron transport chain in mitochondria. The encoded protein associates with the inner membrane of the mitochondrion where it accepts electrons from cytochrome b and transfers them to the cytochrome oxidase complex. This protein is also involved in initiation of apoptosis. Mutations in this gene are associated with autosomal dominant nonsyndromic thrombocytopenia. Numerous processed pseudogenes of this gene are found throughout the human genome.[provided by RefSeq, Jul 2010]","start":25120091,"end":25125361,"strand":-1,"description":"cytochrome c, somatic [Source:HGNC Symbol;Acc:HGNC:19986]"}, {"versioned_ensembl_gene_id":"ENSG00000282797.1","gene_symbol":"IGHJ6","gene_name":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28475","summary":null,"start":105863969,"end":105864031,"strand":-1,"description":"immunoglobulin heavy joining 6 [Source:HGNC Symbol;Acc:HGNC:5540]"}, {"versioned_ensembl_gene_id":"ENSG00000273760.1","gene_symbol":"AC245041.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47970043,"end":47973496,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106211.8","gene_symbol":"HSPB1","gene_name":"heat shock protein family B (small) member 1 [Source:HGNC Symbol;Acc:HGNC:5246]","synonyms":"HSP28,HSP27,Hsp25,Hs.76067,CMT2F","biotype":"protein_coding","ncbi_id":"3315","summary":"This gene encodes a member of the small heat shock protein (HSP20) family of proteins. In response to environmental stress, the encoded protein translocates from the cytoplasm to the nucleus and functions as a molecular chaperone that promotes the correct folding of other proteins. This protein plays an important role in the differentiation of a wide variety of cell types. Expression of this gene is correlated with poor clinical outcome in multiple human cancers, and the encoded protein may promote cancer cell proliferation and metastasis, while protecting cancer cells from apoptosis. Mutations in this gene have been identified in human patients with Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. [provided by RefSeq, Aug 2017]","start":76302544,"end":76304295,"strand":1,"description":"heat shock protein family B (small) member 1 [Source:HGNC Symbol;Acc:HGNC:5246]"}, {"versioned_ensembl_gene_id":"ENSG00000250830.1","gene_symbol":"MRPS35P2","gene_name":"mitochondrial ribosomal protein S35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29769]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359778","summary":null,"start":98402542,"end":98402732,"strand":-1,"description":"mitochondrial ribosomal protein S35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29769]"}, {"versioned_ensembl_gene_id":"ENSG00000132330.16","gene_symbol":"SCLY","gene_name":"selenocysteine lyase [Source:HGNC Symbol;Acc:HGNC:18161]","synonyms":"SCL","biotype":"protein_coding","ncbi_id":"51540","summary":"Selenocysteine lyase (SCLY; EC 4.4.1.16) catalyzes the pyridoxal 5-prime phosphate-dependent conversion of L-selenocysteine to L-alanine and elemental selenium (Mihara et al., 2000 [PubMed 10692412]).[supplied by OMIM, Mar 2008]","start":238060889,"end":238099413,"strand":1,"description":"selenocysteine lyase [Source:HGNC Symbol;Acc:HGNC:18161]"}, {"versioned_ensembl_gene_id":"ENSG00000205808.5","gene_symbol":"PLPP6","gene_name":"phospholipid phosphatase 6 [Source:HGNC Symbol;Acc:HGNC:23682]","synonyms":"PPAPDC2,PDP1,FLJ90191,FLJ46512","biotype":"protein_coding","ncbi_id":"403313","summary":null,"start":4662315,"end":4665258,"strand":1,"description":"phospholipid phosphatase 6 [Source:HGNC Symbol;Acc:HGNC:23682]"}, {"versioned_ensembl_gene_id":"ENSG00000084234.16","gene_symbol":"APLP2","gene_name":"amyloid beta precursor like protein 2 [Source:HGNC Symbol;Acc:HGNC:598]","synonyms":"APPL2,APPH","biotype":"protein_coding","ncbi_id":"334","summary":"This gene encodes amyloid precursor- like protein 2 (APLP2), which is a member of the APP (amyloid precursor protein) family including APP, APLP1 and APLP2. This protein is ubiquitously expressed. It contains heparin-, copper- and zinc- binding domains at the N-terminus, BPTI/Kunitz inhibitor and E2 domains in the middle region, and transmembrane and intracellular domains at the C-terminus. This protein interacts with major histocompatibility complex (MHC) class I molecules. The synergy of this protein and the APP is required to mediate neuromuscular transmission, spatial learning and synaptic plasticity. This protein has been implicated in the pathogenesis of Alzheimer's disease. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":130069837,"end":130144811,"strand":1,"description":"amyloid beta precursor like protein 2 [Source:HGNC Symbol;Acc:HGNC:598]"}, {"versioned_ensembl_gene_id":"ENSG00000160050.14","gene_symbol":"CCDC28B","gene_name":"coiled-coil domain containing 28B [Source:HGNC Symbol;Acc:HGNC:28163]","synonyms":"RP4-622L5.5,MGC1203","biotype":"protein_coding","ncbi_id":"79140","summary":"The product of this gene localizes to centrosomes and basal bodies. The protein colocalizes with several proteins associated with Bardet-Biedl syndrome (BBS) and participates in the regulation of cilia development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":32200386,"end":32205387,"strand":1,"description":"coiled-coil domain containing 28B [Source:HGNC Symbol;Acc:HGNC:28163]"}, {"versioned_ensembl_gene_id":"ENSG00000230969.2","gene_symbol":"LINC02090","gene_name":"long intergenic non-protein coding RNA 2090 [Source:HGNC Symbol;Acc:HGNC:52941]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371562","summary":null,"start":16988329,"end":16990177,"strand":1,"description":"long intergenic non-protein coding RNA 2090 [Source:HGNC Symbol;Acc:HGNC:52941]"}, {"versioned_ensembl_gene_id":"ENSG00000248202.1","gene_symbol":"LINC02234","gene_name":"long intergenic non-protein coding RNA 2234 [Source:HGNC Symbol;Acc:HGNC:53105]","synonyms":"RP11-455B3.1","biotype":"lincRNA","ncbi_id":"109729164","summary":null,"start":97881420,"end":97922695,"strand":1,"description":"long intergenic non-protein coding RNA 2234 [Source:HGNC Symbol;Acc:HGNC:53105]"}, {"versioned_ensembl_gene_id":"ENSG00000259786.6","gene_symbol":"LINC02109","gene_name":"long intergenic non-protein coding RNA 2109 [Source:HGNC Symbol;Acc:HGNC:52964]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929660","summary":null,"start":29143503,"end":29217115,"strand":1,"description":"long intergenic non-protein coding RNA 2109 [Source:HGNC Symbol;Acc:HGNC:52964]"}, {"versioned_ensembl_gene_id":"ENSG00000141977.9","gene_symbol":"CIB3","gene_name":"calcium and integrin binding family member 3 [Source:HGNC Symbol;Acc:HGNC:24580]","synonyms":"KIP3","biotype":"protein_coding","ncbi_id":"117286","summary":"This gene product shares a high degree of sequence similarity with DNA-dependent protein kinase catalytic subunit-interacting protein 2 in human and mouse, and like them may bind the catalytic subunit of DNA-dependent protein kinases. The exact function of this gene is not known. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":16161368,"end":16173525,"strand":-1,"description":"calcium and integrin binding family member 3 [Source:HGNC Symbol;Acc:HGNC:24580]"}, {"versioned_ensembl_gene_id":"ENSG00000248687.2","gene_symbol":"AC024589.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29104880,"end":29105438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204291.10","gene_symbol":"COL15A1","gene_name":"collagen type XV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2192]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1306","summary":"This gene encodes the alpha chain of type XV collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Type XV collagen has a wide tissue distribution but the strongest expression is localized to basement membrane zones so it may function to adhere basement membranes to underlying connective tissue stroma. The proteolytically produced C-terminal fragment of type XV collagen is restin, a potentially antiangiogenic protein that is closely related to endostatin. Mouse studies have shown that collagen XV deficiency is associated with muscle and microvessel deterioration. [provided by RefSeq, May 2013]","start":98943179,"end":99070792,"strand":1,"description":"collagen type XV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2192]"}, {"versioned_ensembl_gene_id":"ENSG00000133704.9","gene_symbol":"IPO8","gene_name":"importin 8 [Source:HGNC Symbol;Acc:HGNC:9853]","synonyms":"RANBP8,IMP8","biotype":"protein_coding","ncbi_id":"10526","summary":"The importin-alpha/beta complex and the GTPase Ran mediate nuclear import of proteins with a classical nuclear localization signal. The protein encoded by this gene is a member of a class of approximately 20 potential Ran targets that share a sequence motif related to the Ran-binding site of importin-beta. This protein binds to the nuclear pore complex and, along with RanGTP and RANBP1, inhibits the GAP stimulation of the Ran GTPase. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":30628988,"end":30695986,"strand":-1,"description":"importin 8 [Source:HGNC Symbol;Acc:HGNC:9853]"}, {"versioned_ensembl_gene_id":"ENSG00000250799.9","gene_symbol":"PRODH2","gene_name":"proline dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:17325]","synonyms":"HSPOX1","biotype":"protein_coding","ncbi_id":"58510","summary":"The protein encoded by this gene catalyzes the first step in the catabolism of trans-4-hydroxy-L-proline, an amino acid derivative obtained through food intake and collagen turnover. One of the downstream products of this catabolism is glyoxylate, which in people with disorders of glyoxalate metabolism can lead to an increase in oxalate levels and the formation of calcium-oxalate kidney stones. Therefore, this gene may serve as a therapeutic target against primary hyperoxalurias (PH). This gene is similar to proline dehydrogenase (oxidase) 1, a mitochondrial enzyme that catalyzes the first step in proline catabolism. [provided by RefSeq, Jan 2017]","start":35799988,"end":35813299,"strand":-1,"description":"proline dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:17325]"}, {"versioned_ensembl_gene_id":"ENSG00000230201.5","gene_symbol":"ATP6V0CP1","gene_name":"ATPase H+ transporting V0 subunit c pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31323]","synonyms":"ATCD1","biotype":"processed_pseudogene","ncbi_id":"100132978","summary":null,"start":4856757,"end":4857374,"strand":-1,"description":"ATPase H+ transporting V0 subunit c pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31323]"}, {"versioned_ensembl_gene_id":"ENSG00000162461.7","gene_symbol":"SLC25A34","gene_name":"solute carrier family 25 member 34 [Source:HGNC Symbol;Acc:HGNC:27653]","synonyms":"DKFZp781A10161","biotype":"protein_coding","ncbi_id":"284723","summary":"SLC25A34 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":15736405,"end":15741396,"strand":1,"description":"solute carrier family 25 member 34 [Source:HGNC Symbol;Acc:HGNC:27653]"}, {"versioned_ensembl_gene_id":"ENSG00000125385.9","gene_symbol":"AL161781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37046835,"end":37047237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267245.1","gene_symbol":"AC008805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32824142,"end":32824505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278518.1","gene_symbol":"AL161645.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133526259,"end":133527513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231148.1","gene_symbol":"HMGB1P7","gene_name":"high mobility group box 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39096]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420044","summary":null,"start":31913143,"end":31913754,"strand":1,"description":"high mobility group box 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39096]"}, {"versioned_ensembl_gene_id":"ENSG00000277878.1","gene_symbol":"AC010385.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28927298,"end":28927459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162685.6","gene_symbol":"LSP1P3","gene_name":"lymphocyte-specific protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729862","summary":null,"start":28926816,"end":28927023,"strand":1,"description":"lymphocyte-specific protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39718]"}, {"versioned_ensembl_gene_id":"ENSG00000250453.1","gene_symbol":"AC008825.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28782678,"end":28809249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270495.1","gene_symbol":"AC008825.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28808538,"end":28809255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226696.5","gene_symbol":"LENG8-AS1","gene_name":"LENG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40705]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355426","summary":null,"start":54444813,"end":54449045,"strand":-1,"description":"LENG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40705]"}, {"versioned_ensembl_gene_id":"ENSG00000235681.1","gene_symbol":"AC245884.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54446830,"end":54447047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260190.1","gene_symbol":"AL807752.5","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":136937169,"end":136937988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163823.3","gene_symbol":"CCR1","gene_name":"C-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:1602]","synonyms":"SCYAR1,MIP1aR,CMKBR1,CKR-1,CD191","biotype":"protein_coding","ncbi_id":"1230","summary":"This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. The ligands of this receptor include macrophage inflammatory protein 1 alpha (MIP-1 alpha), regulated on activation normal T expressed and secreted protein (RANTES), monocyte chemoattractant protein 3 (MCP-3), and myeloid progenitor inhibitory factor-1 (MPIF-1). Chemokines and their receptors mediated signal transduction are critical for the recruitment of effector immune cells to the site of inflammation. Knockout studies of the mouse homolog suggested the roles of this gene in host protection from inflammatory response, and susceptibility to virus and parasite. This gene and other chemokine receptor genes, including CCR2, CCRL2, CCR3, CCR5 and CCXCR1, are found to form a gene cluster on chromosome 3p. [provided by RefSeq, Jul 2008]","start":46201709,"end":46208396,"strand":-1,"description":"C-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:1602]"}, {"versioned_ensembl_gene_id":"ENSG00000266079.4","gene_symbol":"SNORA59B","gene_name":"small nucleolar RNA, H/ACA box 59B [Source:HGNC Symbol;Acc:HGNC:32658]","synonyms":"ACA59","biotype":"snoRNA","ncbi_id":"677882","summary":null,"start":19557211,"end":19557911,"strand":1,"description":"small nucleolar RNA, H/ACA box 59B [Source:HGNC Symbol;Acc:HGNC:32658]"}, {"versioned_ensembl_gene_id":"ENSG00000213549.3","gene_symbol":"AC005077.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76113026,"end":76113400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197353.3","gene_symbol":"LYPD2","gene_name":"LY6/PLAUR domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25215]","synonyms":"UNQ430,RGTR430,LYPDC2","biotype":"protein_coding","ncbi_id":"137797","summary":null,"start":142750150,"end":142752534,"strand":-1,"description":"LY6/PLAUR domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25215]"}, {"versioned_ensembl_gene_id":"ENSG00000270019.1","gene_symbol":"AC110769.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113888203,"end":113889750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165188.13","gene_symbol":"RNF183","gene_name":"ring finger protein 183 [Source:HGNC Symbol;Acc:HGNC:28721]","synonyms":"MGC4734","biotype":"protein_coding","ncbi_id":"138065","summary":null,"start":113297093,"end":113303376,"strand":-1,"description":"ring finger protein 183 [Source:HGNC Symbol;Acc:HGNC:28721]"}, {"versioned_ensembl_gene_id":"ENSG00000236449.1","gene_symbol":"AC010894.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174547141,"end":174774827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236500.1","gene_symbol":"CD24P1","gene_name":"CD24 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1646]","synonyms":"CD24L1","biotype":"processed_pseudogene","ncbi_id":"935","summary":null,"start":15614643,"end":15614867,"strand":-1,"description":"CD24 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1646]"}, {"versioned_ensembl_gene_id":"ENSG00000251401.2","gene_symbol":"AC093729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90682996,"end":90683123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276063.1","gene_symbol":"AL391262.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69154311,"end":69154804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261302.5","gene_symbol":"AC106779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56708772,"end":56729968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182318.5","gene_symbol":"ZSCAN22","gene_name":"zinc finger and SCAN domain containing 22 [Source:HGNC Symbol;Acc:HGNC:4929]","synonyms":"ZNF50,HKR2","biotype":"protein_coding","ncbi_id":"342945","summary":null,"start":58327019,"end":58342332,"strand":1,"description":"zinc finger and SCAN domain containing 22 [Source:HGNC Symbol;Acc:HGNC:4929]"}, {"versioned_ensembl_gene_id":"ENSG00000082212.12","gene_symbol":"ME2","gene_name":"malic enzyme 2 [Source:HGNC Symbol;Acc:HGNC:6984]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4200","summary":"This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene. [provided by RefSeq, Dec 2009]","start":50878734,"end":50954257,"strand":1,"description":"malic enzyme 2 [Source:HGNC Symbol;Acc:HGNC:6984]"}, {"versioned_ensembl_gene_id":"ENSG00000258842.1","gene_symbol":"AL390816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62069518,"end":62081154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258311.5","gene_symbol":"AC009779.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55716036,"end":55724703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269944.1","gene_symbol":"AP001267.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":118415977,"end":118416521,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250775.1","gene_symbol":"AC093730.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63468701,"end":63494278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256355.1","gene_symbol":"NTAN1P3","gene_name":"N-terminal asparagine amidase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45263]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420356","summary":null,"start":67424272,"end":67424986,"strand":-1,"description":"N-terminal asparagine amidase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45263]"}, {"versioned_ensembl_gene_id":"ENSG00000189050.15","gene_symbol":"RNFT1","gene_name":"ring finger protein, transmembrane 1 [Source:HGNC Symbol;Acc:HGNC:30206]","synonyms":"PTD016","biotype":"protein_coding","ncbi_id":"51136","summary":null,"start":59952240,"end":59964761,"strand":-1,"description":"ring finger protein, transmembrane 1 [Source:HGNC Symbol;Acc:HGNC:30206]"}, {"versioned_ensembl_gene_id":"ENSG00000138722.9","gene_symbol":"MMRN1","gene_name":"multimerin 1 [Source:HGNC Symbol;Acc:HGNC:7178]","synonyms":"EMILIN4,ECM,MMRN,GPIa*","biotype":"protein_coding","ncbi_id":"22915","summary":" Multimerin is a massive, soluble protein found in platelets and in the endothelium of blood vessels. It is comprised of subunits linked by interchain disulfide bonds to form large, variably sized homomultimers. Multimerin is a factor V/Va-binding protein and may function as a carrier protein for platelet factor V. It may also have functions as an extracellular matrix or adhesive protein. Recently, patients with an unusual autosomal-dominant bleeding disorder (factor V Quebec) were found to have a deficiency of platelet multimerin. [provided by RefSeq, Jul 2008]","start":89879532,"end":89954629,"strand":1,"description":"multimerin 1 [Source:HGNC Symbol;Acc:HGNC:7178]"}, {"versioned_ensembl_gene_id":"ENSG00000260036.1","gene_symbol":"AC013355.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55442635,"end":55443357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272810.1","gene_symbol":"U91328.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26013241,"end":26013757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224447.1","gene_symbol":"U91328.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26016379,"end":26016601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276907.4","gene_symbol":"ARHGAP27","gene_name":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]","synonyms":"SH3P20,SH3D20,FLJ43547,CAMGAP1","biotype":"protein_coding","ncbi_id":"201176","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may pay a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2013]","start":45393902,"end":45434423,"strand":-1,"description":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]"}, {"versioned_ensembl_gene_id":"ENSG00000227207.2","gene_symbol":"RPL31P12","gene_name":"ribosomal protein L31 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35546]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270887","summary":null,"start":72301472,"end":72301829,"strand":1,"description":"ribosomal protein L31 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35546]"}, {"versioned_ensembl_gene_id":"ENSG00000245662.3","gene_symbol":"LINC02211","gene_name":"long intergenic non-protein coding RNA 2211 [Source:HGNC Symbol;Acc:HGNC:53078]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374693","summary":null,"start":25187800,"end":25324386,"strand":1,"description":"long intergenic non-protein coding RNA 2211 [Source:HGNC Symbol;Acc:HGNC:53078]"}, {"versioned_ensembl_gene_id":"ENSG00000179988.13","gene_symbol":"PSTK","gene_name":"phosphoseryl-tRNA kinase [Source:HGNC Symbol;Acc:HGNC:28578]","synonyms":"MGC35392,C10orf89","biotype":"protein_coding","ncbi_id":"118672","summary":null,"start":122954381,"end":122997513,"strand":1,"description":"phosphoseryl-tRNA kinase [Source:HGNC Symbol;Acc:HGNC:28578]"}, {"versioned_ensembl_gene_id":"ENSG00000278053.4","gene_symbol":"DDX52","gene_name":"DExD-box helicase 52 [Source:HGNC Symbol;Acc:HGNC:20038]","synonyms":"ROK1","biotype":"protein_coding","ncbi_id":"11056","summary":null,"start":37609739,"end":37643464,"strand":-1,"description":"DExD-box helicase 52 [Source:HGNC Symbol;Acc:HGNC:20038]"}, {"versioned_ensembl_gene_id":"ENSG00000216471.3","gene_symbol":"RPSAP43","gene_name":"ribosomal protein SA pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35501]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643954","summary":null,"start":114084168,"end":114084792,"strand":-1,"description":"ribosomal protein SA pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35501]"}, {"versioned_ensembl_gene_id":"ENSG00000235135.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32457148,"end":32460324,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000254690.1","gene_symbol":"AC233992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144314590,"end":144315138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203757.2","gene_symbol":"OR6K3","gene_name":"olfactory receptor family 6 subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:15030]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391114","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158716327,"end":158720720,"strand":-1,"description":"olfactory receptor family 6 subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:15030]"}, {"versioned_ensembl_gene_id":"ENSG00000276012.1","gene_symbol":"AL160153.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101717564,"end":101723106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198919.12","gene_symbol":"DZIP3","gene_name":"DAZ interacting zinc finger protein 3 [Source:HGNC Symbol;Acc:HGNC:30938]","synonyms":"PPP1R66,hRUL138","biotype":"protein_coding","ncbi_id":"9666","summary":null,"start":108589682,"end":108694846,"strand":1,"description":"DAZ interacting zinc finger protein 3 [Source:HGNC Symbol;Acc:HGNC:30938]"}, {"versioned_ensembl_gene_id":"ENSG00000235221.1","gene_symbol":"AL355478.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69311333,"end":69322101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229136.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29475093,"end":29476139,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000111530.12","gene_symbol":"CAND1","gene_name":"cullin associated and neddylation dissociated 1 [Source:HGNC Symbol;Acc:HGNC:30688]","synonyms":"TIP120A,TIP120,KIAA0829,DKFZp434M1414","biotype":"protein_coding","ncbi_id":"55832","summary":"This gene encodes an essential regulator of Cullin-RING ubiquitin ligases, which are in involved in ubiquitinylation of proteins degraded by the Ub proteasome system. The encoded protein binds to unneddylated cullin-RING box protein complexes and acts as an inhibitor of cullin neddylation and of Skp1, cullin, and F box ubiquitin ligase complex assembly and activity. In mammalian cell culture, this protein predominantly localizes to the cytoplasm. Knockdown of this gene in preadipocytes results in blocked adipogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":67269281,"end":67319951,"strand":1,"description":"cullin associated and neddylation dissociated 1 [Source:HGNC Symbol;Acc:HGNC:30688]"}, {"versioned_ensembl_gene_id":"ENSG00000172828.12","gene_symbol":"CES3","gene_name":"carboxylesterase 3 [Source:HGNC Symbol;Acc:HGNC:1865]","synonyms":"FLJ21736,ES31","biotype":"protein_coding","ncbi_id":"23491","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene is expressed in several tissues, particularly in colon, trachea and in brain, and the protein participates in colon and neural drug metabolism. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported, but the biological validity and/or full-length nature of some variants have not been determined.[provided by RefSeq, Jun 2010]","start":66961237,"end":66975148,"strand":1,"description":"carboxylesterase 3 [Source:HGNC Symbol;Acc:HGNC:1865]"}, {"versioned_ensembl_gene_id":"ENSG00000270139.1","gene_symbol":"AP001172.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16417139,"end":16419080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135744.7","gene_symbol":"AGT","gene_name":"angiotensinogen [Source:HGNC Symbol;Acc:HGNC:333]","synonyms":"SERPINA8","biotype":"protein_coding","ncbi_id":"183","summary":"The protein encoded by this gene, pre-angiotensinogen or angiotensinogen precursor, is expressed in the liver and is cleaved by the enzyme renin in response to lowered blood pressure. The resulting product, angiotensin I, is then cleaved by angiotensin converting enzyme (ACE) to generate the physiologically active enzyme angiotensin II. The protein is involved in maintaining blood pressure, body fluid and electrolyte homeostasis, and in the pathogenesis of essential hypertension and preeclampsia. Mutations in this gene are associated with susceptibility to essential hypertension, and can cause renal tubular dysgenesis, a severe disorder of renal tubular development. Defects in this gene have also been associated with non-familial structural atrial fibrillation, and inflammatory bowel disease. [provided by RefSeq, Nov 2019]","start":230702523,"end":230714297,"strand":-1,"description":"angiotensinogen [Source:HGNC Symbol;Acc:HGNC:333]"}, {"versioned_ensembl_gene_id":"ENSG00000254486.1","gene_symbol":"LINC02547","gene_name":"long intergenic non-protein coding RNA 2547 [Source:HGNC Symbol;Acc:HGNC:53582]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376554","summary":null,"start":12030875,"end":12061785,"strand":1,"description":"long intergenic non-protein coding RNA 2547 [Source:HGNC Symbol;Acc:HGNC:53582]"}, {"versioned_ensembl_gene_id":"ENSG00000100347.14","gene_symbol":"SAMM50","gene_name":"SAMM50 sorting and assembly machinery component [Source:HGNC Symbol;Acc:HGNC:24276]","synonyms":"YNL026W,TRG-3,TOB55,SAM50,OMP85,CGI-51","biotype":"protein_coding","ncbi_id":"25813","summary":"This gene encodes a component of the Sorting and Assembly Machinery (SAM) of the mitochondrial outer membrane. The Sam complex functions in the assembly of beta-barrel proteins into the outer mitochondrial membrane.[provided by RefSeq, Jun 2011]","start":43955421,"end":44010531,"strand":1,"description":"SAMM50 sorting and assembly machinery component [Source:HGNC Symbol;Acc:HGNC:24276]"}, {"versioned_ensembl_gene_id":"ENSG00000198841.3","gene_symbol":"KTI12","gene_name":"KTI12 chromatin associated homolog [Source:HGNC Symbol;Acc:HGNC:25160]","synonyms":"TOT4,SBBI81,MGC20419","biotype":"protein_coding","ncbi_id":"112970","summary":null,"start":52032103,"end":52033816,"strand":-1,"description":"KTI12 chromatin associated homolog [Source:HGNC Symbol;Acc:HGNC:25160]"}, {"versioned_ensembl_gene_id":"ENSG00000198856.12","gene_symbol":"OSTC","gene_name":"oligosaccharyltransferase complex non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:24448]","synonyms":"DC2","biotype":"protein_coding","ncbi_id":"58505","summary":null,"start":108650584,"end":108667820,"strand":1,"description":"oligosaccharyltransferase complex non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:24448]"}, {"versioned_ensembl_gene_id":"ENSG00000225354.1","gene_symbol":"RPL7AP52","gene_name":"ribosomal protein L7a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36233]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271534","summary":null,"start":94882554,"end":94883343,"strand":1,"description":"ribosomal protein L7a pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36233]"}, {"versioned_ensembl_gene_id":"ENSG00000232131.1","gene_symbol":"NCOA7-AS1","gene_name":"NCOA7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40954]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355145","summary":null,"start":125797856,"end":125818858,"strand":-1,"description":"NCOA7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40954]"}, {"versioned_ensembl_gene_id":"ENSG00000272360.1","gene_symbol":"AC116036.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58490830,"end":58491291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170454.5","gene_symbol":"KRT75","gene_name":"keratin 75 [Source:HGNC Symbol;Acc:HGNC:24431]","synonyms":"K6HF","biotype":"protein_coding","ncbi_id":"9119","summary":"This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. This gene is expressed in the companion layer, upper germinative matrix region of the hair follicle, and medulla of the hair shaft. The encoded protein plays an essential role in hair and nail formation. Variations in this gene have been associated with the hair disorders pseudofolliculitis barbae (PFB) and loose anagen hair syndrome (LAHS). [provided by RefSeq, Oct 2008]","start":52424070,"end":52434525,"strand":-1,"description":"keratin 75 [Source:HGNC Symbol;Acc:HGNC:24431]"}, {"versioned_ensembl_gene_id":"ENSG00000229749.1","gene_symbol":"COTL1P1","gene_name":"coactosin-like F-actin binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2086]","synonyms":"CLPSMCR","biotype":"processed_pseudogene","ncbi_id":"27170","summary":null,"start":16853935,"end":16854309,"strand":1,"description":"coactosin-like F-actin binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2086]"}, {"versioned_ensembl_gene_id":"ENSG00000283033.1","gene_symbol":"AC022596.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16861146,"end":16864223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176641.10","gene_symbol":"RNF152","gene_name":"ring finger protein 152 [Source:HGNC Symbol;Acc:HGNC:26811]","synonyms":"FLJ39176","biotype":"protein_coding","ncbi_id":"220441","summary":null,"start":61808063,"end":61894247,"strand":-1,"description":"ring finger protein 152 [Source:HGNC Symbol;Acc:HGNC:26811]"}, {"versioned_ensembl_gene_id":"ENSG00000131686.14","gene_symbol":"CA6","gene_name":"carbonic anhydrase 6 [Source:HGNC Symbol;Acc:HGNC:1380]","synonyms":null,"biotype":"protein_coding","ncbi_id":"765","summary":"The protein encoded by this gene is one of several isozymes of carbonic anhydrase. This protein is found only in salivary glands and saliva and protein may play a role in the reversible hydratation of carbon dioxide though its function in saliva is unknown. [provided by RefSeq, Jul 2008]","start":8945867,"end":8975092,"strand":1,"description":"carbonic anhydrase 6 [Source:HGNC Symbol;Acc:HGNC:1380]"}, {"versioned_ensembl_gene_id":"ENSG00000197969.11","gene_symbol":"VPS13A","gene_name":"vacuolar protein sorting 13 homolog A [Source:HGNC Symbol;Acc:HGNC:1908]","synonyms":"KIAA0986,CHAC","biotype":"protein_coding","ncbi_id":"23230","summary":"The protein encoded by this gene may control steps in the cycling of proteins through the trans-Golgi network to endosomes, lysosomes and the plasma membrane. Mutations in this gene cause the autosomal recessive disorder, chorea-acanthocytosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":77177353,"end":77421541,"strand":1,"description":"vacuolar protein sorting 13 homolog A [Source:HGNC Symbol;Acc:HGNC:1908]"}, {"versioned_ensembl_gene_id":"ENSG00000265853.1","gene_symbol":"AL353996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16893198,"end":16893429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218893.1","gene_symbol":"SUMO2P12","gene_name":"SUMO2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480262","summary":null,"start":12319453,"end":12319592,"strand":1,"description":"SUMO2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49350]"}, {"versioned_ensembl_gene_id":"ENSG00000212802.4","gene_symbol":"RPL15P3","gene_name":"ribosomal protein L15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21538]","synonyms":"bA511S14.1","biotype":"processed_pseudogene","ncbi_id":"653232","summary":null,"start":12514110,"end":12514724,"strand":1,"description":"ribosomal protein L15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21538]"}, {"versioned_ensembl_gene_id":"ENSG00000241764.3","gene_symbol":"AC002467.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107742817,"end":107744581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234015.1","gene_symbol":"LINC02530","gene_name":"long intergenic non-protein coding RNA 2530 [Source:HGNC Symbol;Acc:HGNC:53556]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928309","summary":null,"start":12582915,"end":12585404,"strand":-1,"description":"long intergenic non-protein coding RNA 2530 [Source:HGNC Symbol;Acc:HGNC:53556]"}, {"versioned_ensembl_gene_id":"ENSG00000257500.1","gene_symbol":"AC055736.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52407580,"end":52428494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241634.1","gene_symbol":"AC069499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108543367,"end":108543875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257844.2","gene_symbol":"KRT90P","gene_name":"keratin 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:30195]","synonyms":"KRTHBP1,KRT124P,HBA","biotype":"unprocessed_pseudogene","ncbi_id":"85340","summary":null,"start":52411742,"end":52421867,"strand":-1,"description":"keratin 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:30195]"}, {"versioned_ensembl_gene_id":"ENSG00000105879.11","gene_symbol":"CBLL1","gene_name":"Cbl proto-oncogene like 1 [Source:HGNC Symbol;Acc:HGNC:21225]","synonyms":"RNF188,HAKAI,FLJ23109","biotype":"protein_coding","ncbi_id":"79872","summary":"This gene encodes an E3 ubiquitin-ligase for the E-cadherin complex and mediates its ubiquitination, endocytosis, and degradation in the lysosomes. The encoded protein contains a RING-finger domain and is also thought to have a role in control of cell proliferation. A related pseudogene has been identified on chromosome X. Alternative splicing results in a non-coding transcript variant. [provided by RefSeq, Aug 2011]","start":107743697,"end":107761667,"strand":1,"description":"Cbl proto-oncogene like 1 [Source:HGNC Symbol;Acc:HGNC:21225]"}, {"versioned_ensembl_gene_id":"ENSG00000203865.9","gene_symbol":"ATP1A1-AS1","gene_name":"ATP1A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28262]","synonyms":"MGC16179,C1orf203,ATP1A1OS","biotype":"processed_transcript","ncbi_id":"84852","summary":null,"start":116392247,"end":116418622,"strand":-1,"description":"ATP1A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28262]"}, {"versioned_ensembl_gene_id":"ENSG00000274581.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":91718574,"end":91718789,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252156.1","gene_symbol":"RNU6-155P","gene_name":"RNA, U6 small nuclear 155, pseudogene [Source:HGNC Symbol;Acc:HGNC:47118]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481224","summary":null,"start":75768059,"end":75768158,"strand":-1,"description":"RNA, U6 small nuclear 155, pseudogene [Source:HGNC Symbol;Acc:HGNC:47118]"}, {"versioned_ensembl_gene_id":"ENSG00000212542.1","gene_symbol":"RNA5SP496","gene_name":"RNA, 5S ribosomal pseudogene 496 [Source:HGNC Symbol;Acc:HGNC:43396]","synonyms":"RN5S496","biotype":"rRNA","ncbi_id":"100873738","summary":null,"start":31305404,"end":31305512,"strand":1,"description":"RNA, 5S ribosomal pseudogene 496 [Source:HGNC Symbol;Acc:HGNC:43396]"}, {"versioned_ensembl_gene_id":"ENSG00000207002.1","gene_symbol":"SNORA5","gene_name":"Small nucleolar RNA SNORA5 [Source:RFAM;Acc:RF00392]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":123814077,"end":123814207,"strand":1,"description":"Small nucleolar RNA SNORA5 [Source:RFAM;Acc:RF00392]"}, {"versioned_ensembl_gene_id":"ENSG00000206596.1","gene_symbol":"RNU1-27P","gene_name":"RNA, U1 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:37497]","synonyms":"RNU1-7P","biotype":"snRNA","ncbi_id":"26865","summary":null,"start":34546714,"end":34546877,"strand":1,"description":"RNA, U1 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:37497]"}, {"versioned_ensembl_gene_id":"ENSG00000276003.1","gene_symbol":"FAM13A-AS1_2","gene_name":"FAM13A antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02115]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88723209,"end":88723316,"strand":1,"description":"FAM13A antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02115]"}, {"versioned_ensembl_gene_id":"ENSG00000266255.1","gene_symbol":"MIR4475","gene_name":"microRNA 4475 [Source:HGNC Symbol;Acc:HGNC:41697]","synonyms":"hsa-mir-4475","biotype":"miRNA","ncbi_id":"100616289","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36823539,"end":36823599,"strand":-1,"description":"microRNA 4475 [Source:HGNC Symbol;Acc:HGNC:41697]"}, {"versioned_ensembl_gene_id":"ENSG00000284179.1","gene_symbol":"MIR7-1","gene_name":"microRNA 7-1 [Source:HGNC Symbol;Acc:HGNC:31638]","synonyms":"MIRN7-1,hsa-mir-7-1","biotype":"miRNA","ncbi_id":"407043","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":83969748,"end":83969857,"strand":-1,"description":"microRNA 7-1 [Source:HGNC Symbol;Acc:HGNC:31638]"}, {"versioned_ensembl_gene_id":"ENSG00000206690.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88099995,"end":88100105,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263407.1","gene_symbol":"MIR4660","gene_name":"microRNA 4660 [Source:HGNC Symbol;Acc:HGNC:41861]","synonyms":"hsa-mir-4660","biotype":"miRNA","ncbi_id":"100616350","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9048445,"end":9048518,"strand":1,"description":"microRNA 4660 [Source:HGNC Symbol;Acc:HGNC:41861]"}, {"versioned_ensembl_gene_id":"ENSG00000277118.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":186076306,"end":186076591,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201774.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":10901978,"end":10902074,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264379.1","gene_symbol":"SNORD39","gene_name":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":21524307,"end":21524382,"strand":-1,"description":"Small nucleolar RNA SNORD55/SNORD39 [Source:RFAM;Acc:RF00157]"}, {"versioned_ensembl_gene_id":"ENSG00000253001.1","gene_symbol":"RN7SKP105","gene_name":"RNA, 7SK small nuclear pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:45829]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479141","summary":null,"start":163828800,"end":163829113,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 105 [Source:HGNC Symbol;Acc:HGNC:45829]"}, {"versioned_ensembl_gene_id":"ENSG00000200610.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":106515897,"end":106515998,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263458.1","gene_symbol":"MIR4455","gene_name":"microRNA 4455 [Source:HGNC Symbol;Acc:HGNC:41536]","synonyms":"hsa-mir-4455","biotype":"miRNA","ncbi_id":"100616111","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":184938383,"end":184938440,"strand":-1,"description":"microRNA 4455 [Source:HGNC Symbol;Acc:HGNC:41536]"}, {"versioned_ensembl_gene_id":"ENSG00000238406.1","gene_symbol":"RNU7-171P","gene_name":"RNA, U7 small nuclear 171 pseudogene [Source:HGNC Symbol;Acc:HGNC:45705]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479089","summary":null,"start":128543916,"end":128543977,"strand":1,"description":"RNA, U7 small nuclear 171 pseudogene [Source:HGNC Symbol;Acc:HGNC:45705]"}, {"versioned_ensembl_gene_id":"ENSG00000273501.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":27382801,"end":27382907,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000238645.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":53334562,"end":53334664,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000277035.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28134408,"end":28134585,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000274883.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45931806,"end":45932083,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265439.2","gene_symbol":"RN7SL811P","gene_name":"RNA, 7SL, cytoplasmic 811, pseudogene [Source:HGNC Symbol;Acc:HGNC:46827]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479517","summary":null,"start":44209766,"end":44210063,"strand":1,"description":"RNA, 7SL, cytoplasmic 811, pseudogene [Source:HGNC Symbol;Acc:HGNC:46827]"}, {"versioned_ensembl_gene_id":"ENSG00000242653.3","gene_symbol":"RN7SL132P","gene_name":"RNA, 7SL, cytoplasmic 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:46148]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479270","summary":null,"start":34753424,"end":34753719,"strand":1,"description":"RNA, 7SL, cytoplasmic 132, pseudogene [Source:HGNC Symbol;Acc:HGNC:46148]"}, {"versioned_ensembl_gene_id":"ENSG00000238711.1","gene_symbol":"RNY4P25","gene_name":"RNA, Ro-associated Y4 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42475]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862665","summary":null,"start":151439000,"end":151439095,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42475]"}, {"versioned_ensembl_gene_id":"ENSG00000202125.1","gene_symbol":"RNU1-100P","gene_name":"RNA, U1 small nuclear 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:48442]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480183","summary":null,"start":142420205,"end":142420369,"strand":-1,"description":"RNA, U1 small nuclear 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:48442]"}, {"versioned_ensembl_gene_id":"ENSG00000251904.1","gene_symbol":"RNA5SP272","gene_name":"RNA, 5S ribosomal pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:43172]","synonyms":"RN5S272","biotype":"rRNA","ncbi_id":"100873525","summary":null,"start":88396437,"end":88396547,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 272 [Source:HGNC Symbol;Acc:HGNC:43172]"}, {"versioned_ensembl_gene_id":"ENSG00000201198.1","gene_symbol":"RNU6-879P","gene_name":"RNA, U6 small nuclear 879, pseudogene [Source:HGNC Symbol;Acc:HGNC:47842]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481456","summary":null,"start":57415296,"end":57415403,"strand":1,"description":"RNA, U6 small nuclear 879, pseudogene [Source:HGNC Symbol;Acc:HGNC:47842]"}, {"versioned_ensembl_gene_id":"ENSG00000273660.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30294670,"end":30294906,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252420.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61739127,"end":61739229,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251951.1","gene_symbol":"RN7SKP34","gene_name":"RNA, 7SK small nuclear pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:45758]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479110","summary":null,"start":87102603,"end":87102846,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:45758]"}, {"versioned_ensembl_gene_id":"ENSG00000252288.1","gene_symbol":"RNU6-966P","gene_name":"RNA, U6 small nuclear 966, pseudogene [Source:HGNC Symbol;Acc:HGNC:47929]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480625","summary":null,"start":44973558,"end":44973661,"strand":1,"description":"RNA, U6 small nuclear 966, pseudogene [Source:HGNC Symbol;Acc:HGNC:47929]"}, {"versioned_ensembl_gene_id":"ENSG00000222974.1","gene_symbol":"RN7SKP228","gene_name":"RNA, 7SK small nuclear pseudogene 228 [Source:HGNC Symbol;Acc:HGNC:45952]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479196","summary":null,"start":12876684,"end":12876946,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 228 [Source:HGNC Symbol;Acc:HGNC:45952]"}, {"versioned_ensembl_gene_id":"ENSG00000201021.1","gene_symbol":"RNU6-743P","gene_name":"RNA, U6 small nuclear 743, pseudogene [Source:HGNC Symbol;Acc:HGNC:47706]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480605","summary":null,"start":43405473,"end":43405578,"strand":1,"description":"RNA, U6 small nuclear 743, pseudogene [Source:HGNC Symbol;Acc:HGNC:47706]"}, {"versioned_ensembl_gene_id":"ENSG00000201476.1","gene_symbol":"RNA5SP353","gene_name":"RNA, 5S ribosomal pseudogene 353 [Source:HGNC Symbol;Acc:HGNC:43253]","synonyms":"RN5S353","biotype":"rRNA","ncbi_id":"100873613","summary":null,"start":13440884,"end":13441001,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 353 [Source:HGNC Symbol;Acc:HGNC:43253]"}, {"versioned_ensembl_gene_id":"ENSG00000239579.3","gene_symbol":"RN7SL325P","gene_name":"RNA, 7SL, cytoplasmic 325, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000212626.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":7301020,"end":7301153,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000206746.1","gene_symbol":"RNU6-142P","gene_name":"RNA, U6 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:47105]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479628","summary":null,"start":62731226,"end":62731332,"strand":-1,"description":"RNA, U6 small nuclear 142, pseudogene [Source:HGNC Symbol;Acc:HGNC:47105]"}, {"versioned_ensembl_gene_id":"ENSG00000222072.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100907174,"end":100907280,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202078.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":160326104,"end":160326216,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252170.2","gene_symbol":"SNORD112","gene_name":"Small nucleolar RNA SNORD112 [Source:RFAM;Acc:RF01169]","synonyms":"14q(0)","biotype":"snoRNA","ncbi_id":"692215","summary":"Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":129518576,"end":129518647,"strand":1,"description":"Small nucleolar RNA SNORD112 [Source:RFAM;Acc:RF01169]"}, {"versioned_ensembl_gene_id":"ENSG00000264417.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal 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{"versioned_ensembl_gene_id":"ENSG00000274607.1","gene_symbol":"RNU6-866P","gene_name":"RNA, U6 small nuclear 866, pseudogene [Source:HGNC Symbol;Acc:HGNC:47829]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481454","summary":null,"start":38755279,"end":38755400,"strand":-1,"description":"RNA, U6 small nuclear 866, pseudogene [Source:HGNC Symbol;Acc:HGNC:47829]"}, {"versioned_ensembl_gene_id":"ENSG00000242066.3","gene_symbol":"RN7SL214P","gene_name":"RNA, 7SL, cytoplasmic 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:46230]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479300","summary":null,"start":77916718,"end":77916982,"strand":-1,"description":"RNA, 7SL, cytoplasmic 214, pseudogene [Source:HGNC Symbol;Acc:HGNC:46230]"}, {"versioned_ensembl_gene_id":"ENSG00000222983.1","gene_symbol":"RNA5SP127","gene_name":"RNA, 5S ribosomal pseudogene 127 [Source:HGNC Symbol;Acc:HGNC:43027]","synonyms":"RN5S127","biotype":"rRNA","ncbi_id":"100873397","summary":null,"start":31228715,"end":31228847,"strand":1,"description":"RNA, 5S ribosomal pseudogene 127 [Source:HGNC Symbol;Acc:HGNC:43027]"}, {"versioned_ensembl_gene_id":"ENSG00000206652.1","gene_symbol":"RNU1-1","gene_name":"RNA, U1 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10120]","synonyms":"U1A1,U1,RNU1G4,RNU1A3,Rnu1a1,RNU1A,RNU1,HU1-1,HSD1","biotype":"snRNA","ncbi_id":"26871","summary":null,"start":16514122,"end":16514285,"strand":-1,"description":"RNA, U1 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10120]"}, {"versioned_ensembl_gene_id":"ENSG00000275698.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30506091,"end":30506195,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207412.1","gene_symbol":"RNU6-455P","gene_name":"RNA, U6 small nuclear 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[Source:HGNC Symbol;Acc:HGNC:32146]","synonyms":"hsa-mir-509-1,hsa-mir-509,MIRN509-1,MIRN509","biotype":"miRNA","ncbi_id":"574514","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147260532,"end":147260625,"strand":-1,"description":"microRNA 509-1 [Source:HGNC Symbol;Acc:HGNC:32146]"}, {"versioned_ensembl_gene_id":"ENSG00000200243.1","gene_symbol":"RN7SKP79","gene_name":"RNA, 7SK small nuclear pseudogene 79 [Source:HGNC Symbol;Acc:HGNC:45803]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480857","summary":null,"start":6848127,"end":6848462,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 79 [Source:HGNC Symbol;Acc:HGNC:45803]"}, {"versioned_ensembl_gene_id":"ENSG00000207755.3","gene_symbol":"MIR450A2","gene_name":"microRNA 450a-2 [Source:HGNC Symbol;Acc:HGNC:32137]","synonyms":"MIRN450A2,MIRN450-2,hsa-mir-450a-2,hsa-mir-450-2","biotype":"miRNA","ncbi_id":"574505","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134540508,"end":134540607,"strand":-1,"description":"microRNA 450a-2 [Source:HGNC Symbol;Acc:HGNC:32137]"}, {"versioned_ensembl_gene_id":"ENSG00000264653.1","gene_symbol":"MIR5194","gene_name":"microRNA 5194 [Source:HGNC Symbol;Acc:HGNC:43498]","synonyms":"hsa-mir-5194","biotype":"miRNA","ncbi_id":"100847051","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130008334,"end":130008453,"strand":-1,"description":"microRNA 5194 [Source:HGNC Symbol;Acc:HGNC:43498]"}, {"versioned_ensembl_gene_id":"ENSG00000265660.1","gene_symbol":"MIR4664","gene_name":"microRNA 4664 [Source:HGNC Symbol;Acc:HGNC:41777]","synonyms":"hsa-mir-4664","biotype":"miRNA","ncbi_id":"100616318","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143733083,"end":143733153,"strand":-1,"description":"microRNA 4664 [Source:HGNC Symbol;Acc:HGNC:41777]"}, {"versioned_ensembl_gene_id":"ENSG00000222230.1","gene_symbol":"RNA5SP158","gene_name":"RNA, 5S ribosomal pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:43058]","synonyms":"RN5S158","biotype":"rRNA","ncbi_id":"100873424","summary":null,"start":38758791,"end":38758892,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 158 [Source:HGNC Symbol;Acc:HGNC:43058]"}, {"versioned_ensembl_gene_id":"ENSG00000207026.1","gene_symbol":"RNU6-472P","gene_name":"RNA, U6 small nuclear 472, pseudogene [Source:HGNC Symbol;Acc:HGNC:47435]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481328","summary":null,"start":33923374,"end":33923480,"strand":-1,"description":"RNA, U6 small nuclear 472, pseudogene [Source:HGNC Symbol;Acc:HGNC:47435]"}, {"versioned_ensembl_gene_id":"ENSG00000252558.1","gene_symbol":"RNU6-914P","gene_name":"RNA, U6 small nuclear 914, pseudogene [Source:HGNC Symbol;Acc:HGNC:47877]","synonyms":null,"biotype":"snRNA","ncbi_id":"107063540","summary":null,"start":98192205,"end":98192313,"strand":-1,"description":"RNA, U6 small nuclear 914, pseudogene [Source:HGNC Symbol;Acc:HGNC:47877]"}, {"versioned_ensembl_gene_id":"ENSG00000207547.1","gene_symbol":"MIR25","gene_name":"microRNA 25 [Source:HGNC Symbol;Acc:HGNC:31609]","synonyms":"MIRN25,hsa-mir-25","biotype":"miRNA","ncbi_id":"407014","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100093560,"end":100093643,"strand":-1,"description":"microRNA 25 [Source:HGNC Symbol;Acc:HGNC:31609]"}, {"versioned_ensembl_gene_id":"ENSG00000208014.1","gene_symbol":"MIR653","gene_name":"microRNA 653 [Source:HGNC Symbol;Acc:HGNC:32909]","synonyms":"MIRN653,hsa-mir-653","biotype":"miRNA","ncbi_id":"724023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93482760,"end":93482855,"strand":-1,"description":"microRNA 653 [Source:HGNC Symbol;Acc:HGNC:32909]"}, {"versioned_ensembl_gene_id":"ENSG00000212555.1","gene_symbol":"RNU6-192P","gene_name":"RNA, U6 small nuclear 192, pseudogene [Source:HGNC Symbol;Acc:HGNC:47155]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481237","summary":null,"start":17903762,"end":17903861,"strand":1,"description":"RNA, U6 small nuclear 192, pseudogene [Source:HGNC Symbol;Acc:HGNC:47155]"}, {"versioned_ensembl_gene_id":"ENSG00000242811.3","gene_symbol":"RN7SL229P","gene_name":"RNA, 7SL, cytoplasmic 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:46245]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479305","summary":null,"start":180736405,"end":180736703,"strand":-1,"description":"RNA, 7SL, cytoplasmic 229, pseudogene [Source:HGNC Symbol;Acc:HGNC:46245]"}, {"versioned_ensembl_gene_id":"ENSG00000283829.1","gene_symbol":"MIR378I","gene_name":"microRNA 378i [Source:HGNC Symbol;Acc:HGNC:41620]","synonyms":"hsa-mir-378i","biotype":"miRNA","ncbi_id":"100616259","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41923222,"end":41923297,"strand":-1,"description":"microRNA 378i [Source:HGNC Symbol;Acc:HGNC:41620]"}, {"versioned_ensembl_gene_id":"ENSG00000216101.3","gene_symbol":"MIR877","gene_name":"microRNA 877 [Source:HGNC Symbol;Acc:HGNC:33660]","synonyms":"MIRN877,hsa-mir-877","biotype":"miRNA","ncbi_id":"100126314","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30584332,"end":30584417,"strand":1,"description":"microRNA 877 [Source:HGNC Symbol;Acc:HGNC:33660]"}, {"versioned_ensembl_gene_id":"ENSG00000207296.1","gene_symbol":"RNU6-140P","gene_name":"RNA, U6 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:47103]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481221","summary":null,"start":38797002,"end":38797109,"strand":-1,"description":"RNA, U6 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:47103]"}, {"versioned_ensembl_gene_id":"ENSG00000266211.1","gene_symbol":"MIR3156-3","gene_name":"microRNA 3156-3 [Source:HGNC Symbol;Acc:HGNC:38229]","synonyms":"hsa-mir-3156-3","biotype":"miRNA","ncbi_id":"100423018","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13406384,"end":13406460,"strand":-1,"description":"microRNA 3156-3 [Source:HGNC Symbol;Acc:HGNC:38229]"}, {"versioned_ensembl_gene_id":"ENSG00000199024.1","gene_symbol":"MIR103A2","gene_name":"microRNA 103a-2 [Source:HGNC Symbol;Acc:HGNC:31491]","synonyms":"hsa-mir-103-2,MIRN103-2,MIR103-2,hsa-mir-103a-2","biotype":"miRNA","ncbi_id":"406896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3917494,"end":3917571,"strand":1,"description":"microRNA 103a-2 [Source:HGNC Symbol;Acc:HGNC:31491]"}, {"versioned_ensembl_gene_id":"ENSG00000201898.1","gene_symbol":"SNORA72","gene_name":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]","synonyms":"RNU72,U72","biotype":"snoRNA","ncbi_id":"26775","summary":null,"start":224179641,"end":224179767,"strand":1,"description":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]"}, {"versioned_ensembl_gene_id":"ENSG00000275711.1","gene_symbol":"MIR6795","gene_name":"microRNA 6795 [Source:HGNC Symbol;Acc:HGNC:50031]","synonyms":"hsa-mir-6795","biotype":"miRNA","ncbi_id":"102465476","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15179283,"end":15179350,"strand":-1,"description":"microRNA 6795 [Source:HGNC Symbol;Acc:HGNC:50031]"}, {"versioned_ensembl_gene_id":"ENSG00000223247.1","gene_symbol":"RNU2-64P","gene_name":"RNA, U2 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48557]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481654","summary":null,"start":73110992,"end":73111182,"strand":1,"description":"RNA, U2 small nuclear 64, pseudogene [Source:HGNC Symbol;Acc:HGNC:48557]"}, {"versioned_ensembl_gene_id":"ENSG00000207702.1","gene_symbol":"MIR211","gene_name":"microRNA 211 [Source:HGNC Symbol;Acc:HGNC:31588]","synonyms":"MIRN211,hsa-mir-211","biotype":"miRNA","ncbi_id":"406993","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31065032,"end":31065141,"strand":-1,"description":"microRNA 211 [Source:HGNC Symbol;Acc:HGNC:31588]"}, {"versioned_ensembl_gene_id":"ENSG00000240692.3","gene_symbol":"RN7SL538P","gene_name":"RNA, 7SL, cytoplasmic 538, pseudogene [Source:HGNC Symbol;Acc:HGNC:46554]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480517","summary":null,"start":69879592,"end":69879895,"strand":1,"description":"RNA, 7SL, cytoplasmic 538, pseudogene [Source:HGNC Symbol;Acc:HGNC:46554]"}, {"versioned_ensembl_gene_id":"ENSG00000252105.1","gene_symbol":"RNU1-143P","gene_name":"RNA, U1 small nuclear 143, pseudogene [Source:HGNC Symbol;Acc:HGNC:48485]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481634","summary":null,"start":143791542,"end":143791687,"strand":-1,"description":"RNA, U1 small nuclear 143, pseudogene [Source:HGNC Symbol;Acc:HGNC:48485]"}, {"versioned_ensembl_gene_id":"ENSG00000207947.3","gene_symbol":"MIR152","gene_name":"microRNA 152 [Source:HGNC Symbol;Acc:HGNC:31538]","synonyms":"MIRN152,hsa-mir-152","biotype":"miRNA","ncbi_id":"406943","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48037161,"end":48037247,"strand":-1,"description":"microRNA 152 [Source:HGNC Symbol;Acc:HGNC:31538]"}, {"versioned_ensembl_gene_id":"ENSG00000276225.1","gene_symbol":"MEG8_1","gene_name":"Maternally expressed 8 exon 1 [Source:RFAM;Acc:RF02145]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100894817,"end":100894913,"strand":1,"description":"Maternally expressed 8 exon 1 [Source:RFAM;Acc:RF02145]"}, {"versioned_ensembl_gene_id":"ENSG00000264295.1","gene_symbol":"MIR3922","gene_name":"microRNA 3922 [Source:HGNC Symbol;Acc:HGNC:38895]","synonyms":"hsa-mir-3922","biotype":"miRNA","ncbi_id":"100500843","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104591633,"end":104591716,"strand":1,"description":"microRNA 3922 [Source:HGNC Symbol;Acc:HGNC:38895]"}, {"versioned_ensembl_gene_id":"ENSG00000264800.1","gene_symbol":"MIR4294","gene_name":"microRNA 4294 [Source:HGNC Symbol;Acc:HGNC:38180]","synonyms":"hsa-mir-4294","biotype":"miRNA","ncbi_id":"100422895","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48985512,"end":48985587,"strand":-1,"description":"microRNA 4294 [Source:HGNC Symbol;Acc:HGNC:38180]"}, {"versioned_ensembl_gene_id":"ENSG00000278265.1","gene_symbol":"MIR6770-1","gene_name":"microRNA 6770-1 [Source:HGNC Symbol;Acc:HGNC:50223]","synonyms":"hsa-mir-6770-1","biotype":"miRNA","ncbi_id":"102465461","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14930820,"end":14930879,"strand":1,"description":"microRNA 6770-1 [Source:HGNC Symbol;Acc:HGNC:50223]"}, {"versioned_ensembl_gene_id":"ENSG00000264720.3","gene_symbol":"MIR3117","gene_name":"microRNA 3117 [Source:HGNC Symbol;Acc:HGNC:38385]","synonyms":"hsa-mir-3117","biotype":"miRNA","ncbi_id":"100422871","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66628440,"end":66628517,"strand":1,"description":"microRNA 3117 [Source:HGNC Symbol;Acc:HGNC:38385]"}, {"versioned_ensembl_gene_id":"ENSG00000212461.1","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":71639355,"end":71639483,"strand":1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000252016.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":88148792,"end":88148918,"strand":1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000239472.3","gene_symbol":"RN7SL221P","gene_name":"RNA, 7SL, cytoplasmic 221, pseudogene [Source:HGNC Symbol;Acc:HGNC:46237]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480982","summary":null,"start":5918564,"end":5918844,"strand":-1,"description":"RNA, 7SL, cytoplasmic 221, pseudogene [Source:HGNC Symbol;Acc:HGNC:46237]"}, {"versioned_ensembl_gene_id":"ENSG00000283507.1","gene_symbol":"MIR1302-1","gene_name":"microRNA 1302-1 [Source:HGNC Symbol;Acc:HGNC:35293]","synonyms":"MIRN1302-1,hsa-mir-1302-1","biotype":"miRNA","ncbi_id":"100302227","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112695034,"end":112695176,"strand":-1,"description":"microRNA 1302-1 [Source:HGNC Symbol;Acc:HGNC:35293]"}, {"versioned_ensembl_gene_id":"ENSG00000199506.1","gene_symbol":"RNU6-247P","gene_name":"RNA, U6 small nuclear 247, pseudogene [Source:HGNC Symbol;Acc:HGNC:47210]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479676","summary":null,"start":95792529,"end":95792635,"strand":-1,"description":"RNA, U6 small nuclear 247, pseudogene [Source:HGNC Symbol;Acc:HGNC:47210]"}, {"versioned_ensembl_gene_id":"ENSG00000284503.1","gene_symbol":"MIR3652","gene_name":"microRNA 3652 [Source:HGNC Symbol;Acc:HGNC:38894]","synonyms":"hsa-mir-3652","biotype":"miRNA","ncbi_id":"100500842","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":103930425,"end":103930555,"strand":1,"description":"microRNA 3652 [Source:HGNC Symbol;Acc:HGNC:38894]"}, {"versioned_ensembl_gene_id":"ENSG00000252822.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":236060677,"end":236060772,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221783.1","gene_symbol":"MIR1183","gene_name":"microRNA 1183 [Source:HGNC Symbol;Acc:HGNC:35264]","synonyms":"MIRN1183,hsa-mir-1183","biotype":"miRNA","ncbi_id":"100302122","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21471058,"end":21471146,"strand":1,"description":"microRNA 1183 [Source:HGNC Symbol;Acc:HGNC:35264]"}, {"versioned_ensembl_gene_id":"ENSG00000284224.1","gene_symbol":"MIR937","gene_name":"microRNA 937 [Source:HGNC Symbol;Acc:HGNC:33680]","synonyms":"MIRN937,hsa-mir-937","biotype":"miRNA","ncbi_id":"100126338","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143812957,"end":143813042,"strand":-1,"description":"microRNA 937 [Source:HGNC Symbol;Acc:HGNC:33680]"}, {"versioned_ensembl_gene_id":"ENSG00000252979.1","gene_symbol":"RNU6-165P","gene_name":"RNA, U6 small nuclear 165, pseudogene [Source:HGNC Symbol;Acc:HGNC:47128]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481227","summary":null,"start":53766534,"end":53766632,"strand":-1,"description":"RNA, U6 small nuclear 165, pseudogene [Source:HGNC Symbol;Acc:HGNC:47128]"}, {"versioned_ensembl_gene_id":"ENSG00000251916.1","gene_symbol":"RNU1-61P","gene_name":"RNA, U1 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:48403]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481980","summary":null,"start":32549940,"end":32550090,"strand":-1,"description":"RNA, U1 small nuclear 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:48403]"}, {"versioned_ensembl_gene_id":"ENSG00000207333.1","gene_symbol":"RNU6-680P","gene_name":"RNA, U6 small nuclear 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:47643]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480601","summary":null,"start":75709495,"end":75709599,"strand":-1,"description":"RNA, U6 small nuclear 680, pseudogene [Source:HGNC Symbol;Acc:HGNC:47643]"}, {"versioned_ensembl_gene_id":"ENSG00000243702.3","gene_symbol":"RN7SL638P","gene_name":"RNA, 7SL, cytoplasmic 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:46654]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479455","summary":null,"start":18592330,"end":18592619,"strand":1,"description":"RNA, 7SL, cytoplasmic 638, pseudogene [Source:HGNC Symbol;Acc:HGNC:46654]"}, {"versioned_ensembl_gene_id":"ENSG00000207756.1","gene_symbol":"MIR580","gene_name":"microRNA 580 [Source:HGNC Symbol;Acc:HGNC:32836]","synonyms":"MIRN580,hsa-mir-580","biotype":"miRNA","ncbi_id":"693165","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36147892,"end":36147988,"strand":-1,"description":"microRNA 580 [Source:HGNC Symbol;Acc:HGNC:32836]"}, {"versioned_ensembl_gene_id":"ENSG00000215961.1","gene_symbol":"MIR297","gene_name":"microRNA 297 [Source:HGNC Symbol;Acc:HGNC:33691]","synonyms":"MIRN297,hsa-mir-297","biotype":"miRNA","ncbi_id":"100126354","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110860582,"end":110860647,"strand":-1,"description":"microRNA 297 [Source:HGNC Symbol;Acc:HGNC:33691]"}, {"versioned_ensembl_gene_id":"ENSG00000252578.1","gene_symbol":"RNU6-135P","gene_name":"RNA, U6 small nuclear 135, pseudogene [Source:HGNC Symbol;Acc:HGNC:47098]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479625","summary":null,"start":23163953,"end":23164053,"strand":1,"description":"RNA, U6 small nuclear 135, pseudogene [Source:HGNC Symbol;Acc:HGNC:47098]"}, {"versioned_ensembl_gene_id":"ENSG00000266421.3","gene_symbol":"MIR4451","gene_name":"microRNA 4451 [Source:HGNC Symbol;Acc:HGNC:41858]","synonyms":"hsa-mir-4451","biotype":"miRNA","ncbi_id":"100616349","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85722468,"end":85722533,"strand":1,"description":"microRNA 4451 [Source:HGNC Symbol;Acc:HGNC:41858]"}, {"versioned_ensembl_gene_id":"ENSG00000207568.1","gene_symbol":"MIR203A","gene_name":"microRNA 203a [Source:HGNC Symbol;Acc:HGNC:31581]","synonyms":"hsa-mir-203,MIRN203,MIR203","biotype":"miRNA","ncbi_id":"406986","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104117405,"end":104117514,"strand":1,"description":"microRNA 203a [Source:HGNC Symbol;Acc:HGNC:31581]"}, {"versioned_ensembl_gene_id":"ENSG00000199782.1","gene_symbol":"SNORD115-9","gene_name":"small nucleolar RNA, C/D box 115-9 [Source:HGNC Symbol;Acc:HGNC:33028]","synonyms":"HBII-52-9","biotype":"snoRNA","ncbi_id":"100033446","summary":null,"start":25185631,"end":25185712,"strand":1,"description":"small nucleolar RNA, C/D box 115-9 [Source:HGNC Symbol;Acc:HGNC:33028]"}, {"versioned_ensembl_gene_id":"ENSG00000280249.1","gene_symbol":"AL691477.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":134799782,"end":134799945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241159.3","gene_symbol":"RN7SL160P","gene_name":"RNA, 7SL, cytoplasmic 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:46176]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480964","summary":null,"start":70965584,"end":70965867,"strand":1,"description":"RNA, 7SL, cytoplasmic 160, pseudogene [Source:HGNC Symbol;Acc:HGNC:46176]"}, {"versioned_ensembl_gene_id":"ENSG00000252311.1","gene_symbol":"RNU1-103P","gene_name":"RNA, U1 small nuclear 103, pseudogene [Source:HGNC Symbol;Acc:HGNC:48445]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481623","summary":null,"start":85781775,"end":85781899,"strand":-1,"description":"RNA, U1 small nuclear 103, pseudogene [Source:HGNC Symbol;Acc:HGNC:48445]"}, {"versioned_ensembl_gene_id":"ENSG00000239316.3","gene_symbol":"RN7SL11P","gene_name":"RNA, 7SL, cytoplasmic 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46027]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479229","summary":null,"start":89478141,"end":89478433,"strand":1,"description":"RNA, 7SL, cytoplasmic 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:46027]"}, {"versioned_ensembl_gene_id":"ENSG00000253099.1","gene_symbol":"RNU2-60P","gene_name":"RNA, U2 small nuclear 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:48553]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481653","summary":null,"start":111383092,"end":111383219,"strand":1,"description":"RNA, U2 small nuclear 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:48553]"}, {"versioned_ensembl_gene_id":"ENSG00000252125.1","gene_symbol":"RNU6-1299P","gene_name":"RNA, U6 small nuclear 1299, pseudogene [Source:HGNC Symbol;Acc:HGNC:48262]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480133","summary":null,"start":107133071,"end":107133170,"strand":1,"description":"RNA, U6 small nuclear 1299, pseudogene [Source:HGNC Symbol;Acc:HGNC:48262]"}, {"versioned_ensembl_gene_id":"ENSG00000238904.1","gene_symbol":"RNU7-34P","gene_name":"RNA, U7 small nuclear 34 pseudogene [Source:HGNC Symbol;Acc:HGNC:34130]","synonyms":"U7.34","biotype":"snRNA","ncbi_id":"100147821","summary":null,"start":118758211,"end":118758274,"strand":1,"description":"RNA, U7 small nuclear 34 pseudogene [Source:HGNC Symbol;Acc:HGNC:34130]"}, {"versioned_ensembl_gene_id":"ENSG00000276804.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7,PYPAF3","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54956665,"end":54980661,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000274018.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":439297,"end":439397,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200869.1","gene_symbol":"RNU6-457P","gene_name":"RNA, U6 small nuclear 457, pseudogene [Source:HGNC Symbol;Acc:HGNC:47420]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479768","summary":null,"start":6873899,"end":6874005,"strand":1,"description":"RNA, U6 small nuclear 457, pseudogene [Source:HGNC Symbol;Acc:HGNC:47420]"}, {"versioned_ensembl_gene_id":"ENSG00000212036.3","gene_symbol":"MIR548BA","gene_name":"microRNA 548ba [Source:HGNC Symbol;Acc:HGNC:50260]","synonyms":"hsa-mir-548ba","biotype":"miRNA","ncbi_id":"102465854","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49059603,"end":49059658,"strand":1,"description":"microRNA 548ba [Source:HGNC Symbol;Acc:HGNC:50260]"}, {"versioned_ensembl_gene_id":"ENSG00000199001.1","gene_symbol":"MIR448","gene_name":"microRNA 448 [Source:HGNC Symbol;Acc:HGNC:26069]","synonyms":"MIRN448,hsa-mir-448","biotype":"miRNA","ncbi_id":"554212","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114823454,"end":114823564,"strand":1,"description":"microRNA 448 [Source:HGNC Symbol;Acc:HGNC:26069]"}, {"versioned_ensembl_gene_id":"ENSG00000278533.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000212418.1","gene_symbol":"RNY4P36","gene_name":"RNA, Ro-associated Y4 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:50884]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480313","summary":null,"start":76703632,"end":76703727,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:50884]"}, {"versioned_ensembl_gene_id":"ENSG00000212496.1","gene_symbol":"RNU6-1093P","gene_name":"RNA, U6 small nuclear 1093, pseudogene [Source:HGNC Symbol;Acc:HGNC:48056]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481524","summary":null,"start":50256238,"end":50256344,"strand":-1,"description":"RNA, U6 small nuclear 1093, pseudogene [Source:HGNC Symbol;Acc:HGNC:48056]"}, {"versioned_ensembl_gene_id":"ENSG00000275904.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67697076,"end":67697187,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200309.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49132853,"end":49132947,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200174.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62211557,"end":62211666,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206651.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":156484098,"end":156484210,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223188.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":130120806,"end":130120912,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280775.1","gene_symbol":"RNA5SP136","gene_name":"RNA, 5S ribosomal pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:43036]","synonyms":"RN5S136","biotype":"rRNA","ncbi_id":"100873404","summary":null,"start":72692054,"end":72692160,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:43036]"}, {"versioned_ensembl_gene_id":"ENSG00000200305.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39922782,"end":39922886,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263362.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"U52,RNU52,U52,RNU52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31824440,"end":31824506,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000273782.1","gene_symbol":"UCA1","gene_name":"Urothelial cancer associated 1 conserved region [Source:RFAM;Acc:RF02202]","synonyms":"UCAT1,onco-lncRNA-36,LINC00178,CUDR","biotype":"misc_RNA","ncbi_id":"652995","summary":"This gene produces a long non-coding RNA that was found to be upregulated in bladder cancer and plays a regulatory role in cell proliferation. This transcript regulates several genes, including CREB (cAMP responsive element binding protein). Expression of this transcript is regulated by CCAAT/enhancer-binding protein-alpha. [provided by RefSeq, Dec 2017]","start":15834730,"end":15834804,"strand":1,"description":"Urothelial cancer associated 1 conserved region [Source:RFAM;Acc:RF02202]"}, {"versioned_ensembl_gene_id":"ENSG00000239119.1","gene_symbol":"RNU7-119P","gene_name":"RNA, U7 small nuclear 119 pseudogene [Source:HGNC Symbol;Acc:HGNC:45653]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479070","summary":null,"start":73593940,"end":73594002,"strand":-1,"description":"RNA, U7 small nuclear 119 pseudogene [Source:HGNC Symbol;Acc:HGNC:45653]"}, {"versioned_ensembl_gene_id":"ENSG00000220988.1","gene_symbol":"SNORD88C","gene_name":"small nucleolar RNA, C/D box 88C [Source:HGNC Symbol;Acc:HGNC:32749]","synonyms":"HBII-180C","biotype":"snoRNA","ncbi_id":"692204","summary":null,"start":50802328,"end":50802418,"strand":-1,"description":"small nucleolar RNA, C/D box 88C [Source:HGNC Symbol;Acc:HGNC:32749]"}, {"versioned_ensembl_gene_id":"ENSG00000242281.3","gene_symbol":"RN7SL159P","gene_name":"RNA, 7SL, cytoplasmic 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:46175]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479279","summary":null,"start":129370170,"end":129370461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 159, pseudogene [Source:HGNC Symbol;Acc:HGNC:46175]"}, {"versioned_ensembl_gene_id":"ENSG00000266210.2","gene_symbol":"RN7SL371P","gene_name":"RNA, 7SL, cytoplasmic 371, pseudogene [Source:HGNC Symbol;Acc:HGNC:46387]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481839","summary":null,"start":30918469,"end":30918735,"strand":-1,"description":"RNA, 7SL, cytoplasmic 371, pseudogene [Source:HGNC Symbol;Acc:HGNC:46387]"}, {"versioned_ensembl_gene_id":"ENSG00000265195.1","gene_symbol":"MIR4312","gene_name":"microRNA 4312 [Source:HGNC Symbol;Acc:HGNC:38376]","synonyms":"hsa-mir-4312","biotype":"miRNA","ncbi_id":"100422971","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68801850,"end":68801925,"strand":-1,"description":"microRNA 4312 [Source:HGNC Symbol;Acc:HGNC:38376]"}, {"versioned_ensembl_gene_id":"ENSG00000179314.13","gene_symbol":"WSCD1","gene_name":"WSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29060]","synonyms":"KIAA0523","biotype":"protein_coding","ncbi_id":"23302","summary":null,"start":5772234,"end":6124427,"strand":1,"description":"WSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29060]"}, {"versioned_ensembl_gene_id":"ENSG00000277841.1","gene_symbol":"MIR5701-2","gene_name":"microRNA 5701-2 [Source:HGNC Symbol;Acc:HGNC:43510]","synonyms":"hsa-mir-5701-2","biotype":"miRNA","ncbi_id":"100847005","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21513959,"end":21514040,"strand":1,"description":"microRNA 5701-2 [Source:HGNC Symbol;Acc:HGNC:43510]"}, {"versioned_ensembl_gene_id":"ENSG00000240470.3","gene_symbol":"RN7SL346P","gene_name":"RNA, 7SL, cytoplasmic 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:46362]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479350","summary":null,"start":90166233,"end":90166526,"strand":1,"description":"RNA, 7SL, cytoplasmic 346, pseudogene [Source:HGNC Symbol;Acc:HGNC:46362]"}, {"versioned_ensembl_gene_id":"ENSG00000198973.4","gene_symbol":"MIR375","gene_name":"microRNA 375 [Source:HGNC Symbol;Acc:HGNC:31868]","synonyms":"MIRN375,hsa-mir-375","biotype":"miRNA","ncbi_id":"494324","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219001645,"end":219001708,"strand":-1,"description":"microRNA 375 [Source:HGNC Symbol;Acc:HGNC:31868]"}, {"versioned_ensembl_gene_id":"ENSG00000207697.1","gene_symbol":"MIR573","gene_name":"microRNA 573 [Source:HGNC Symbol;Acc:HGNC:32829]","synonyms":"MIRN573,hsa-mir-573","biotype":"miRNA","ncbi_id":"693158","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24520192,"end":24520290,"strand":-1,"description":"microRNA 573 [Source:HGNC Symbol;Acc:HGNC:32829]"}, {"versioned_ensembl_gene_id":"ENSG00000243562.3","gene_symbol":"RN7SL838P","gene_name":"RNA, 7SL, cytoplasmic 838, pseudogene [Source:HGNC Symbol;Acc:HGNC:46854]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479527","summary":null,"start":440399,"end":440693,"strand":-1,"description":"RNA, 7SL, cytoplasmic 838, pseudogene [Source:HGNC Symbol;Acc:HGNC:46854]"}, {"versioned_ensembl_gene_id":"ENSG00000263436.1","gene_symbol":"MIR3158-1","gene_name":"microRNA 3158-1 [Source:HGNC Symbol;Acc:HGNC:38196]","synonyms":"hsa-mir-3158-1","biotype":"miRNA","ncbi_id":"100422900","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101601417,"end":101601497,"strand":1,"description":"microRNA 3158-1 [Source:HGNC Symbol;Acc:HGNC:38196]"}, {"versioned_ensembl_gene_id":"ENSG00000265822.1","gene_symbol":"MIR4422","gene_name":"microRNA 4422 [Source:HGNC Symbol;Acc:HGNC:41654]","synonyms":"hsa-mir-4422","biotype":"miRNA","ncbi_id":"100616272","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55225641,"end":55225723,"strand":1,"description":"microRNA 4422 [Source:HGNC Symbol;Acc:HGNC:41654]"}, {"versioned_ensembl_gene_id":"ENSG00000252190.1","gene_symbol":"SCARNA17","gene_name":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]","synonyms":"mgU12-22/U4-8,U91","biotype":"scaRNA","ncbi_id":"677769","summary":null,"start":26006006,"end":26006130,"strand":1,"description":"small Cajal body-specific RNA 17 [Source:RFAM;Acc:RF00492]"}, {"versioned_ensembl_gene_id":"ENSG00000252501.1","gene_symbol":"RNU4-77P","gene_name":"RNA, U4 small nuclear 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:47013]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481196","summary":null,"start":233448626,"end":233448781,"strand":-1,"description":"RNA, U4 small nuclear 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:47013]"}, {"versioned_ensembl_gene_id":"ENSG00000222755.1","gene_symbol":"RN7SKP206","gene_name":"RNA, 7SK small nuclear pseudogene 206 [Source:HGNC Symbol;Acc:HGNC:45930]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479187","summary":null,"start":129290983,"end":129291275,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 206 [Source:HGNC Symbol;Acc:HGNC:45930]"}, {"versioned_ensembl_gene_id":"ENSG00000207204.1","gene_symbol":"RNU6-393P","gene_name":"RNA, U6 small nuclear 393, pseudogene [Source:HGNC Symbol;Acc:HGNC:47356]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481302","summary":null,"start":98794718,"end":98794824,"strand":-1,"description":"RNA, U6 small nuclear 393, pseudogene [Source:HGNC Symbol;Acc:HGNC:47356]"}, {"versioned_ensembl_gene_id":"ENSG00000243650.3","gene_symbol":"RN7SL834P","gene_name":"RNA, 7SL, cytoplasmic 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:46850]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481148","summary":null,"start":230507101,"end":230507386,"strand":1,"description":"RNA, 7SL, cytoplasmic 834, pseudogene [Source:HGNC Symbol;Acc:HGNC:46850]"}, {"versioned_ensembl_gene_id":"ENSG00000252275.1","gene_symbol":"RNU7-192P","gene_name":"RNA, U7 small nuclear 192 pseudogene [Source:HGNC Symbol;Acc:HGNC:45726]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480833","summary":null,"start":188716665,"end":188716725,"strand":-1,"description":"RNA, U7 small nuclear 192 pseudogene [Source:HGNC Symbol;Acc:HGNC:45726]"}, {"versioned_ensembl_gene_id":"ENSG00000283772.1","gene_symbol":"MIR6778","gene_name":"microRNA 6778 [Source:HGNC Symbol;Acc:HGNC:50183]","synonyms":"hsa-mir-6778","biotype":"miRNA","ncbi_id":"102466733","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18340814,"end":18340886,"strand":-1,"description":"microRNA 6778 [Source:HGNC Symbol;Acc:HGNC:50183]"}, {"versioned_ensembl_gene_id":"ENSG00000283853.1","gene_symbol":"MIR4738","gene_name":"microRNA 4738 [Source:HGNC Symbol;Acc:HGNC:41679]","synonyms":"hsa-mir-4738","biotype":"miRNA","ncbi_id":"100616282","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75784521,"end":75784607,"strand":-1,"description":"microRNA 4738 [Source:HGNC Symbol;Acc:HGNC:41679]"}, {"versioned_ensembl_gene_id":"ENSG00000207725.3","gene_symbol":"MIR222","gene_name":"microRNA 222 [Source:HGNC Symbol;Acc:HGNC:31602]","synonyms":"MIRN222,hsa-mir-222","biotype":"miRNA","ncbi_id":"407007","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45747015,"end":45747124,"strand":-1,"description":"microRNA 222 [Source:HGNC Symbol;Acc:HGNC:31602]"}, {"versioned_ensembl_gene_id":"ENSG00000266287.1","gene_symbol":"MIR3683","gene_name":"microRNA 3683 [Source:HGNC Symbol;Acc:HGNC:38999]","synonyms":"hsa-mir-3683","biotype":"miRNA","ncbi_id":"100500886","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7066964,"end":7067045,"strand":-1,"description":"microRNA 3683 [Source:HGNC Symbol;Acc:HGNC:38999]"}, {"versioned_ensembl_gene_id":"ENSG00000283206.1","gene_symbol":"MIR941-1","gene_name":"microRNA 941-1 [Source:HGNC Symbol;Acc:HGNC:33684]","synonyms":"MIRN941-1,hsa-mir-941-1","biotype":"miRNA","ncbi_id":"100126329","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919449,"end":63919520,"strand":1,"description":"microRNA 941-1 [Source:HGNC Symbol;Acc:HGNC:33684]"}, {"versioned_ensembl_gene_id":"ENSG00000266189.1","gene_symbol":"MIR3186","gene_name":"microRNA 3186 [Source:HGNC Symbol;Acc:HGNC:38311]","synonyms":"hsa-mir-3186","biotype":"miRNA","ncbi_id":"100422944","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81451104,"end":81451188,"strand":-1,"description":"microRNA 3186 [Source:HGNC Symbol;Acc:HGNC:38311]"}, {"versioned_ensembl_gene_id":"ENSG00000159723.4","gene_symbol":"AGRP","gene_name":"agouti related neuropeptide [Source:HGNC Symbol;Acc:HGNC:330]","synonyms":"ASIP2,ART,Agrt","biotype":"protein_coding","ncbi_id":"181","summary":"This gene encodes an antagonist of the melanocortin-3 and melanocortin-4 receptor. It appears to regulate hypothalamic control of feeding behavior via melanocortin receptor and/or intracellular calcium regulation, and thus plays a role in weight homeostasis. Mutations in this gene have been associated with late on-set obesity. [provided by RefSeq, Dec 2009]","start":67482571,"end":67483813,"strand":-1,"description":"agouti related neuropeptide [Source:HGNC Symbol;Acc:HGNC:330]"}, {"versioned_ensembl_gene_id":"ENSG00000267147.2","gene_symbol":"LINC01842","gene_name":"long intergenic non-protein coding RNA 1842 [Source:HGNC Symbol;Acc:HGNC:52656]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928845","summary":null,"start":14333743,"end":14343916,"strand":1,"description":"long intergenic non-protein coding RNA 1842 [Source:HGNC Symbol;Acc:HGNC:52656]"}, {"versioned_ensembl_gene_id":"ENSG00000283346.1","gene_symbol":"MIR6511B2","gene_name":"microRNA 6511b-2 [Source:HGNC Symbol;Acc:HGNC:50230]","synonyms":"hsa-mir-6511b-2","biotype":"miRNA","ncbi_id":"102465985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15134075,"end":15134145,"strand":-1,"description":"microRNA 6511b-2 [Source:HGNC Symbol;Acc:HGNC:50230]"}, {"versioned_ensembl_gene_id":"ENSG00000266307.1","gene_symbol":"MIR5093","gene_name":"microRNA 5093 [Source:HGNC Symbol;Acc:HGNC:43474]","synonyms":"hsa-mir-5093","biotype":"miRNA","ncbi_id":"100847022","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85306226,"end":85306325,"strand":-1,"description":"microRNA 5093 [Source:HGNC Symbol;Acc:HGNC:43474]"}, {"versioned_ensembl_gene_id":"ENSG00000251878.1","gene_symbol":"SNORD79","gene_name":"Small nucleolar RNA SNORD79 [Source:RFAM;Acc:RF00152]","synonyms":null,"biotype":"snoRNA","ncbi_id":"26770","summary":null,"start":184431966,"end":184432049,"strand":1,"description":"Small nucleolar RNA SNORD79 [Source:RFAM;Acc:RF00152]"}, {"versioned_ensembl_gene_id":"ENSG00000202026.1","gene_symbol":"RNU6-1134P","gene_name":"RNA, U6 small nuclear 1134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48097]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480065","summary":null,"start":31713753,"end":31713853,"strand":1,"description":"RNA, U6 small nuclear 1134, pseudogene [Source:HGNC Symbol;Acc:HGNC:48097]"}, {"versioned_ensembl_gene_id":"ENSG00000284229.1","gene_symbol":"MIR6848","gene_name":"microRNA 6848 [Source:HGNC Symbol;Acc:HGNC:50176]","synonyms":"hsa-mir-6848","biotype":"miRNA","ncbi_id":"102465511","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144317246,"end":144317315,"strand":-1,"description":"microRNA 6848 [Source:HGNC Symbol;Acc:HGNC:50176]"}, {"versioned_ensembl_gene_id":"ENSG00000222838.1","gene_symbol":"RNA5SP136","gene_name":"RNA, 5S ribosomal pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:43036]","synonyms":"RN5S136","biotype":"rRNA","ncbi_id":"100873404","summary":null,"start":72691705,"end":72691811,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:43036]"}, {"versioned_ensembl_gene_id":"ENSG00000207132.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30344503,"end":30344604,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000208892.1","gene_symbol":"SNORA49","gene_name":"small nucleolar RNA, H/ACA box 49 [Source:HGNC Symbol;Acc:HGNC:32642]","synonyms":"ACA49","biotype":"snoRNA","ncbi_id":"677829","summary":null,"start":132031224,"end":132031359,"strand":1,"description":"small nucleolar RNA, H/ACA box 49 [Source:HGNC Symbol;Acc:HGNC:32642]"}, {"versioned_ensembl_gene_id":"ENSG00000243738.3","gene_symbol":"RN7SL181P","gene_name":"RNA, 7SL, cytoplasmic 181, pseudogene [Source:HGNC Symbol;Acc:HGNC:46197]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480492","summary":null,"start":121203159,"end":121203435,"strand":1,"description":"RNA, 7SL, cytoplasmic 181, pseudogene [Source:HGNC Symbol;Acc:HGNC:46197]"}, {"versioned_ensembl_gene_id":"ENSG00000264658.1","gene_symbol":"MIR4798","gene_name":"microRNA 4798 [Source:HGNC Symbol;Acc:HGNC:41616]","synonyms":"hsa-mir-4798","biotype":"miRNA","ncbi_id":"100616471","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7310450,"end":7310524,"strand":1,"description":"microRNA 4798 [Source:HGNC Symbol;Acc:HGNC:41616]"}, {"versioned_ensembl_gene_id":"ENSG00000283379.1","gene_symbol":"MIR3688-2","gene_name":"microRNA 3688-2 [Source:HGNC Symbol;Acc:HGNC:41735]","synonyms":"hsa-mir-3688-2","biotype":"miRNA","ncbi_id":"100616303","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159128805,"end":159128891,"strand":1,"description":"microRNA 3688-2 [Source:HGNC Symbol;Acc:HGNC:41735]"}, {"versioned_ensembl_gene_id":"ENSG00000277444.1","gene_symbol":"ZEB2_AS1_4","gene_name":"ZEB2 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF01987]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144521039,"end":144521116,"strand":1,"description":"ZEB2 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF01987]"}, {"versioned_ensembl_gene_id":"ENSG00000207430.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30581184,"end":30581316,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000231343.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33178341,"end":33183793,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000259061.1","gene_symbol":"AL358292.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86936640,"end":86989125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284463.1","gene_symbol":"MIR302B","gene_name":"microRNA 302b [Source:HGNC Symbol;Acc:HGNC:31763]","synonyms":"MIRN302B,hsa-mir-302b","biotype":"miRNA","ncbi_id":"442894","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112648485,"end":112648557,"strand":-1,"description":"microRNA 302b [Source:HGNC Symbol;Acc:HGNC:31763]"}, {"versioned_ensembl_gene_id":"ENSG00000265521.1","gene_symbol":"MIR5697","gene_name":"microRNA 5697 [Source:HGNC Symbol;Acc:HGNC:43509]","synonyms":"hsa-mir-5697","biotype":"miRNA","ncbi_id":"100847055","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9967381,"end":9967458,"strand":1,"description":"microRNA 5697 [Source:HGNC Symbol;Acc:HGNC:43509]"}, {"versioned_ensembl_gene_id":"ENSG00000266781.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33121225,"end":33121320,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252606.1","gene_symbol":"RNU6-1150P","gene_name":"RNA, U6 small nuclear 1150, pseudogene [Source:HGNC Symbol;Acc:HGNC:48113]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480072","summary":null,"start":43996322,"end":43996420,"strand":-1,"description":"RNA, U6 small nuclear 1150, pseudogene [Source:HGNC Symbol;Acc:HGNC:48113]"}, {"versioned_ensembl_gene_id":"ENSG00000277986.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":231711525,"end":231711647,"strand":1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000284557.1","gene_symbol":"MIR1302-10","gene_name":"microRNA 1302-10 [Source:HGNC Symbol;Acc:HGNC:38233]","synonyms":"hsa-mir-1302-10","biotype":"miRNA","ncbi_id":"100422834","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101960459,"end":101960596,"strand":-1,"description":"microRNA 1302-10 [Source:HGNC Symbol;Acc:HGNC:38233]"}, {"versioned_ensembl_gene_id":"ENSG00000277249.1","gene_symbol":"MIR6784","gene_name":"microRNA 6784 [Source:HGNC Symbol;Acc:HGNC:49988]","synonyms":"hsa-mir-6784","biotype":"miRNA","ncbi_id":"102465470","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45114367,"end":45114433,"strand":-1,"description":"microRNA 6784 [Source:HGNC Symbol;Acc:HGNC:49988]"}, {"versioned_ensembl_gene_id":"ENSG00000273944.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55077480,"end":55096373,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000199875.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93719603,"end":93719715,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283262.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":88367793,"end":88367862,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000223336.1","gene_symbol":"RNU2-6P","gene_name":"RNA, U2 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42506]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873825","summary":null,"start":46374401,"end":46374590,"strand":-1,"description":"RNA, U2 small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42506]"}, {"versioned_ensembl_gene_id":"ENSG00000242102.3","gene_symbol":"RN7SL152P","gene_name":"RNA, 7SL, cytoplasmic 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:46168]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480962","summary":null,"start":140577925,"end":140578222,"strand":1,"description":"RNA, 7SL, cytoplasmic 152, pseudogene [Source:HGNC Symbol;Acc:HGNC:46168]"}, {"versioned_ensembl_gene_id":"ENSG00000276782.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":82429872,"end":82430156,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222627.1","gene_symbol":"RNU2-37P","gene_name":"RNA, U2 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:48530]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480213","summary":null,"start":128075073,"end":128075249,"strand":-1,"description":"RNA, U2 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:48530]"}, {"versioned_ensembl_gene_id":"ENSG00000206844.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9874601,"end":9874701,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000253006.1","gene_symbol":"RN7SKP283","gene_name":"RNA, 7SK small nuclear pseudogene 283 [Source:HGNC Symbol;Acc:HGNC:46007]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479221","summary":null,"start":229236340,"end":229236609,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 283 [Source:HGNC Symbol;Acc:HGNC:46007]"}, {"versioned_ensembl_gene_id":"ENSG00000278413.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":26359529,"end":26359702,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000277465.1","gene_symbol":"AL137067.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99368447,"end":99368566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266356.1","gene_symbol":"AC090615.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27411438,"end":27412806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266313.1","gene_symbol":"AC026254.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27333256,"end":27348491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163482.11","gene_symbol":"STK36","gene_name":"serine/threonine kinase 36 [Source:HGNC Symbol;Acc:HGNC:17209]","synonyms":"KIAA1278,FU","biotype":"protein_coding","ncbi_id":"27148","summary":"This gene encodes a member of the serine/threonine kinase family of enzymes. This family member is similar to a Drosophila protein that plays a key role in the Hedgehog signaling pathway. This human protein is a positive regulator of the GLI zinc-finger transcription factors. Knockout studies of the homologous mouse gene suggest that defects in this human gene may lead to congenital hydrocephalus, possibly due to a functional defect in motile cilia. Because Hedgehog signaling is frequently activated in certain kinds of gastrointestinal cancers, it has been suggested that this gene is a target for the treatment of these cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":218672026,"end":218702716,"strand":1,"description":"serine/threonine kinase 36 [Source:HGNC Symbol;Acc:HGNC:17209]"}, {"versioned_ensembl_gene_id":"ENSG00000264837.1","gene_symbol":"AC069061.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27057399,"end":27058221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265646.2","gene_symbol":"AC069061.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27082690,"end":27084036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240219.1","gene_symbol":"AL512306.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204626775,"end":204629712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170382.11","gene_symbol":"LRRN2","gene_name":"leucine rich repeat neuronal 2 [Source:HGNC Symbol;Acc:HGNC:16914]","synonyms":"LRRN5,LRANK1,GAC1,FIGLER7","biotype":"protein_coding","ncbi_id":"10446","summary":"The protein encoded by this gene belongs to the leucine-rich repeat superfamily. This gene was found to be amplified and overexpressed in malignant gliomas. The encoded protein has homology with other proteins that function as cell-adhesion molecules or as signal transduction receptors and is a candidate for the target gene in the 1q32.1 amplicon in malignant gliomas. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":204617170,"end":204685733,"strand":-1,"description":"leucine rich repeat neuronal 2 [Source:HGNC Symbol;Acc:HGNC:16914]"}, {"versioned_ensembl_gene_id":"ENSG00000264970.1","gene_symbol":"AC131274.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22704415,"end":22705685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263609.1","gene_symbol":"LINC02002","gene_name":"long intergenic non-protein coding RNA 2002 [Source:HGNC Symbol;Acc:HGNC:52837]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371595","summary":null,"start":22234328,"end":22266362,"strand":-1,"description":"long intergenic non-protein coding RNA 2002 [Source:HGNC Symbol;Acc:HGNC:52837]"}, {"versioned_ensembl_gene_id":"ENSG00000270788.1","gene_symbol":"PDLIM1P1","gene_name":"PDZ and LIM domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20026]","synonyms":"PDLIM1P","biotype":"processed_pseudogene","ncbi_id":"326616","summary":null,"start":50050368,"end":50051336,"strand":1,"description":"PDZ and LIM domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20026]"}, {"versioned_ensembl_gene_id":"ENSG00000248673.1","gene_symbol":"LINC01331","gene_name":"long intergenic non-protein coding RNA 1331 [Source:HGNC Symbol;Acc:HGNC:50538]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104310351","summary":null,"start":74369376,"end":74536976,"strand":-1,"description":"long intergenic non-protein coding RNA 1331 [Source:HGNC Symbol;Acc:HGNC:50538]"}, {"versioned_ensembl_gene_id":"ENSG00000272780.5","gene_symbol":"AC233702.10","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":21532477,"end":21574517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161682.14","gene_symbol":"FAM171A2","gene_name":"family with sequence similarity 171 member A2 [Source:HGNC Symbol;Acc:HGNC:30480]","synonyms":"MGC34829","biotype":"protein_coding","ncbi_id":"284069","summary":null,"start":44353215,"end":44363875,"strand":-1,"description":"family with sequence similarity 171 member A2 [Source:HGNC Symbol;Acc:HGNC:30480]"}, {"versioned_ensembl_gene_id":"ENSG00000030582.17","gene_symbol":"GRN","gene_name":"granulin precursor [Source:HGNC Symbol;Acc:HGNC:4601]","synonyms":"PGRN,PCDGF,CLN11","biotype":"protein_coding","ncbi_id":"2896","summary":"Granulins are a family of secreted, glycosylated peptides that are cleaved from a single precursor protein with 7.5 repeats of a highly conserved 12-cysteine granulin/epithelin motif. The 88 kDa precursor protein, progranulin, is also called proepithelin and PC cell-derived growth factor. Cleavage of the signal peptide produces mature granulin which can be further cleaved into a variety of active, 6 kDa peptides. These smaller cleavage products are named granulin A, granulin B, granulin C, etc. Epithelins 1 and 2 are synonymous with granulins A and B, respectively. Both the peptides and intact granulin protein regulate cell growth. However, different members of the granulin protein family may act as inhibitors, stimulators, or have dual actions on cell growth. Granulin family members are important in normal development, wound healing, and tumorigenesis. [provided by RefSeq, Jul 2008]","start":44345086,"end":44353102,"strand":1,"description":"granulin precursor [Source:HGNC Symbol;Acc:HGNC:4601]"}, {"versioned_ensembl_gene_id":"ENSG00000249293.1","gene_symbol":"AC091868.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73778039,"end":73786491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126458.3","gene_symbol":"RRAS","gene_name":"related RAS viral (r-ras) oncogene homolog [Source:HGNC Symbol;Acc:HGNC:10447]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6237","summary":"The protein encoded by this gene is a small GTPase involved in diverse processes including angiogenesis, vascular homeostasis and regeneration, cell adhesion, and neuronal axon guidance. Mutations in this gene are found in many invasive cancers. [provided by RefSeq, Jul 2015]","start":49635292,"end":49640201,"strand":-1,"description":"related RAS viral (r-ras) oncogene homolog [Source:HGNC Symbol;Acc:HGNC:10447]"}, {"versioned_ensembl_gene_id":"ENSG00000280474.1","gene_symbol":"AL356481.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":128595893,"end":128596633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250060.1","gene_symbol":"AC122710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6868559,"end":6886787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240991.3","gene_symbol":"RPL23AP67","gene_name":"ribosomal protein L23a pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:36658]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271622","summary":null,"start":133125479,"end":133125952,"strand":1,"description":"ribosomal protein L23a pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:36658]"}, {"versioned_ensembl_gene_id":"ENSG00000214029.4","gene_symbol":"ZNF891","gene_name":"zinc finger protein 891 [Source:HGNC Symbol;Acc:HGNC:38709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060200","summary":null,"start":133106817,"end":133130473,"strand":-1,"description":"zinc finger protein 891 [Source:HGNC Symbol;Acc:HGNC:38709]"}, {"versioned_ensembl_gene_id":"ENSG00000187531.13","gene_symbol":"SIRT7","gene_name":"sirtuin 7 [Source:HGNC Symbol;Acc:HGNC:14935]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51547","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class IV of the sirtuin family. [provided by RefSeq, Jul 2008]","start":81911939,"end":81921323,"strand":-1,"description":"sirtuin 7 [Source:HGNC Symbol;Acc:HGNC:14935]"}, {"versioned_ensembl_gene_id":"ENSG00000108576.9","gene_symbol":"SLC6A4","gene_name":"solute carrier family 6 member 4 [Source:HGNC Symbol;Acc:HGNC:11050]","synonyms":"SERT1,OCD1,HTT,5-HTT","biotype":"protein_coding","ncbi_id":"6532","summary":"This gene encodes an integral membrane protein that transports the neurotransmitter serotonin from synaptic spaces into presynaptic neurons. The encoded protein terminates the action of serotonin and recycles it in a sodium-dependent manner. This protein is a target of psychomotor stimulants, such as amphetamines and cocaine, and is a member of the sodium:neurotransmitter symporter family. A repeat length polymorphism in the promoter of this gene has been shown to affect the rate of serotonin uptake. There have been conflicting results in the literature about the possible effect, if any, that this polymorphism may play in behavior and depression. [provided by RefSeq, May 2019]","start":30194319,"end":30236002,"strand":-1,"description":"solute carrier family 6 member 4 [Source:HGNC Symbol;Acc:HGNC:11050]"}, {"versioned_ensembl_gene_id":"ENSG00000037474.14","gene_symbol":"NSUN2","gene_name":"NOP2/Sun RNA methyltransferase family member 2 [Source:HGNC Symbol;Acc:HGNC:25994]","synonyms":"TRM4,MRT5,Misu,FLJ20303","biotype":"protein_coding","ncbi_id":"54888","summary":"This gene encodes a methyltransferase that catalyzes the methylation of cytosine to 5-methylcytosine (m5C) at position 34 of intron-containing tRNA(Leu)(CAA) precursors. This modification is necessary to stabilize the anticodon-codon pairing and correctly translate the mRNA. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Mar 2011]","start":6599239,"end":6633291,"strand":-1,"description":"NOP2/Sun RNA methyltransferase family member 2 [Source:HGNC Symbol;Acc:HGNC:25994]"}, {"versioned_ensembl_gene_id":"ENSG00000211450.9","gene_symbol":"SELENOH","gene_name":"selenoprotein H [Source:HGNC Symbol;Acc:HGNC:18251]","synonyms":"SELH,C11orf31","biotype":"protein_coding","ncbi_id":"280636","summary":"This gene encodes a nucleolar protein, which belongs to the SelWTH family. It functions as an oxidoreductase, and has been shown to protect neurons against UVB-induced damage by inhibiting apoptotic cell death pathways, promote mitochondrial biogenesis and mitochondrial function, and suppress cellular senescence through genome maintenance and redox regulation. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2016]","start":57741250,"end":57743554,"strand":1,"description":"selenoprotein H [Source:HGNC Symbol;Acc:HGNC:18251]"}, {"versioned_ensembl_gene_id":"ENSG00000213593.9","gene_symbol":"TMX2","gene_name":"thioredoxin related transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30739]","synonyms":"TXNDC14,PDIA12","biotype":"protein_coding","ncbi_id":"51075","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, one transmembrane domain and a C-terminal ER-retention sequence. This protein is enriched on the mitochondria-associated-membrane of the ER via palmitoylation of two of its cytosolically exposed cysteines. [provided by RefSeq, Jan 2017]","start":57712600,"end":57740973,"strand":1,"description":"thioredoxin related transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:30739]"}, {"versioned_ensembl_gene_id":"ENSG00000173992.8","gene_symbol":"CCS","gene_name":"copper chaperone for superoxide dismutase [Source:HGNC Symbol;Acc:HGNC:1613]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9973","summary":"Copper chaperone for superoxide dismutase specifically delivers Cu to copper/zinc superoxide dismutase and may activate copper/zinc superoxide dismutase through direct insertion of the Cu cofactor. [provided by RefSeq, Jul 2008]","start":66592821,"end":66606019,"strand":1,"description":"copper chaperone for superoxide dismutase [Source:HGNC Symbol;Acc:HGNC:1613]"}, {"versioned_ensembl_gene_id":"ENSG00000262413.1","gene_symbol":"AC145207.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81867721,"end":81868552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263859.1","gene_symbol":"AC145207.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81878667,"end":81879557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000062822.12","gene_symbol":"POLD1","gene_name":"DNA polymerase delta 1, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9175]","synonyms":"POLD,CDC2","biotype":"protein_coding","ncbi_id":"5424","summary":"This gene encodes the 125-kDa catalytic subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 6. [provided by RefSeq, Mar 2012]","start":50384204,"end":50418018,"strand":1,"description":"DNA polymerase delta 1, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9175]"}, {"versioned_ensembl_gene_id":"ENSG00000233477.1","gene_symbol":"AL591363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105685383,"end":105685865,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251543.1","gene_symbol":"LINC02230","gene_name":"long intergenic non-protein coding RNA 2230 [Source:HGNC Symbol;Acc:HGNC:53099]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379033","summary":null,"start":73337906,"end":73338533,"strand":1,"description":"long intergenic non-protein coding RNA 2230 [Source:HGNC Symbol;Acc:HGNC:53099]"}, {"versioned_ensembl_gene_id":"ENSG00000226521.7","gene_symbol":"AC087499.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20716481,"end":20737127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224877.3","gene_symbol":"NDUFAF8","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 8 [Source:HGNC Symbol;Acc:HGNC:33551]","synonyms":"C17orf89","biotype":"protein_coding","ncbi_id":"284184","summary":null,"start":81239239,"end":81241281,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 8 [Source:HGNC Symbol;Acc:HGNC:33551]"}, {"versioned_ensembl_gene_id":"ENSG00000262115.1","gene_symbol":"AC027601.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81197393,"end":81200288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258511.1","gene_symbol":"LINC02295","gene_name":"long intergenic non-protein coding RNA 2295 [Source:HGNC Symbol;Acc:HGNC:53211]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370652","summary":null,"start":98136074,"end":98139242,"strand":1,"description":"long intergenic non-protein coding RNA 2295 [Source:HGNC Symbol;Acc:HGNC:53211]"}, {"versioned_ensembl_gene_id":"ENSG00000269392.1","gene_symbol":"AC008655.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50365880,"end":50369331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259097.1","gene_symbol":"AL163932.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98068240,"end":98205143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131398.13","gene_symbol":"KCNC3","gene_name":"potassium voltage-gated channel subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:6235]","synonyms":"SCA13,Kv3.3","biotype":"protein_coding","ncbi_id":"3748","summary":"The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies. Based on sequence similarity, this gene is similar to one of these subfamilies, namely the Shaw subfamily. The protein encoded by this gene belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes. Alternate splicing results in several transcript variants. [provided by RefSeq, Mar 2014]","start":50311937,"end":50333515,"strand":-1,"description":"potassium voltage-gated channel subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:6235]"}, {"versioned_ensembl_gene_id":"ENSG00000258379.1","gene_symbol":"AL355097.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97786565,"end":97789256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246223.8","gene_symbol":"LINC01550","gene_name":"long intergenic non-protein coding RNA 1550 [Source:HGNC Symbol;Acc:HGNC:20111]","synonyms":"C14orf64","biotype":"lincRNA","ncbi_id":"388011","summary":null,"start":97925610,"end":97978124,"strand":-1,"description":"long intergenic non-protein coding RNA 1550 [Source:HGNC Symbol;Acc:HGNC:20111]"}, {"versioned_ensembl_gene_id":"ENSG00000264422.1","gene_symbol":"AC015818.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20576667,"end":20578748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255245.4","gene_symbol":"FXYD6-FXYD2","gene_name":"FXYD6-FXYD2 readthrough [Source:HGNC Symbol;Acc:HGNC:39978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533181","summary":"This locus represents naturally occurring read-through transcription between the neighboring FXYD domain-containing ion transport regulator 6 (GeneID 53826) and sodium/potassium-transporting ATPase subunit gamma (GeneID 486) genes on chromosome 11. One read-through transcript produces a fusion protein that shares sequence identity with each individual gene product, while another read-through transcript encodes a protein that has a distinct C-terminus and only shares sequence identity with the upstream locus (GeneID 53826). [provided by RefSeq, Aug 2011]","start":117820163,"end":117876667,"strand":-1,"description":"FXYD6-FXYD2 readthrough [Source:HGNC Symbol;Acc:HGNC:39978]"}, {"versioned_ensembl_gene_id":"ENSG00000235203.2","gene_symbol":"TBC1D3P3","gene_name":"TBC1 domain family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32408]","synonyms":"USP6P1","biotype":"unprocessed_pseudogene","ncbi_id":"653017","summary":null,"start":20543481,"end":20550963,"strand":-1,"description":"TBC1 domain family member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32408]"}, {"versioned_ensembl_gene_id":"ENSG00000229652.1","gene_symbol":"AL359837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203353365,"end":203353651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263218.2","gene_symbol":"AC127496.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80999509,"end":81000130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226251.5","gene_symbol":"AL451060.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212225278,"end":212238977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270359.1","gene_symbol":"AL358335.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48319068,"end":48319394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170298.15","gene_symbol":"LGALS9B","gene_name":"galectin 9B [Source:HGNC Symbol;Acc:HGNC:24842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284194","summary":"This gene was initially thought to represent a pseudogene of galectin 9; however, this transcript has good exon-intron structure and encodes a predicted protein of the same size as and highly similar to galectin 9. This gene is one of two similar loci on chromosome 17p similar to galectin 9 and now thought to be protein-encoding. This gene is the more centromeric gene. [provided by RefSeq, Jul 2008]","start":20449395,"end":20467539,"strand":-1,"description":"galectin 9B [Source:HGNC Symbol;Acc:HGNC:24842]"}, {"versioned_ensembl_gene_id":"ENSG00000156384.14","gene_symbol":"SFR1","gene_name":"SWI5 dependent homologous recombination repair protein 1 [Source:HGNC Symbol;Acc:HGNC:29574]","synonyms":"MEIR5,MEI5,FLJ41960,C10orf78,bA373N18.1","biotype":"protein_coding","ncbi_id":"119392","summary":null,"start":104122058,"end":104126385,"strand":1,"description":"SWI5 dependent homologous recombination repair protein 1 [Source:HGNC Symbol;Acc:HGNC:29574]"}, {"versioned_ensembl_gene_id":"ENSG00000158458.19","gene_symbol":"NRG2","gene_name":"neuregulin 2 [Source:HGNC Symbol;Acc:HGNC:7998]","synonyms":"NTAK,HRG2,Don-1","biotype":"protein_coding","ncbi_id":"9542","summary":"This gene encodes a novel member of the neuregulin family of growth and differentiation factors. Through interaction with the ERBB family of receptors, this protein induces the growth and differentiation of epithelial, neuronal, glial, and other types of cells. The gene consists of 12 exons and the genomic structure is similar to that of neuregulin 1, another member of the neuregulin family of ligands. The products of these genes mediate distinct biological processes by acting at different sites in tissues and eliciting different biological responses in cells. This gene is located close to the region for demyelinating Charcot-Marie-Tooth disease locus, but is not responsible for this disease. Alternative transcript variants encoding distinct isoforms have been described. [provided by RefSeq, May 2010]","start":139846779,"end":140043299,"strand":-1,"description":"neuregulin 2 [Source:HGNC Symbol;Acc:HGNC:7998]"}, {"versioned_ensembl_gene_id":"ENSG00000100664.10","gene_symbol":"EIF5","gene_name":"eukaryotic translation initiation factor 5 [Source:HGNC Symbol;Acc:HGNC:3299]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1983","summary":"Eukaryotic translation initiation factor-5 (EIF5) interacts with the 40S initiation complex to promote hydrolysis of bound GTP with concomitant joining of the 60S ribosomal subunit to the 40S initiation complex. The resulting functional 80S ribosomal initiation complex is then active in peptidyl transfer and chain elongations (summary by Si et al., 1996 [PubMed 8663286]).[supplied by OMIM, May 2010]","start":103333544,"end":103345025,"strand":1,"description":"eukaryotic translation initiation factor 5 [Source:HGNC Symbol;Acc:HGNC:3299]"}, {"versioned_ensembl_gene_id":"ENSG00000276863.1","gene_symbol":"AC124319.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80333841,"end":80334366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240624.1","gene_symbol":"AL138976.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103282933,"end":103283468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270755.1","gene_symbol":"AL136141.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130044713,"end":130045081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270938.1","gene_symbol":"RAP2CP1","gene_name":"RAP2C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49146]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106480249","summary":null,"start":103279223,"end":103279955,"strand":1,"description":"RAP2C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49146]"}, {"versioned_ensembl_gene_id":"ENSG00000249526.1","gene_symbol":"AC008667.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139684645,"end":139745010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161652.12","gene_symbol":"IZUMO2","gene_name":"IZUMO family member 2 [Source:HGNC Symbol;Acc:HGNC:28518]","synonyms":"SCRL,MGC33947,C19orf41","biotype":"protein_coding","ncbi_id":"126123","summary":null,"start":50152548,"end":50163195,"strand":-1,"description":"IZUMO family member 2 [Source:HGNC Symbol;Acc:HGNC:28518]"}, {"versioned_ensembl_gene_id":"ENSG00000150783.9","gene_symbol":"TEX12","gene_name":"testis expressed 12 [Source:HGNC Symbol;Acc:HGNC:11734]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56158","summary":"This gene is similar to a mouse gene that is expressed in the testis. [provided by RefSeq, Jul 2008]","start":112167372,"end":112172559,"strand":1,"description":"testis expressed 12 [Source:HGNC Symbol;Acc:HGNC:11734]"}, {"versioned_ensembl_gene_id":"ENSG00000226239.1","gene_symbol":"AL031658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32027753,"end":32031575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171302.16","gene_symbol":"CANT1","gene_name":"calcium activated nucleotidase 1 [Source:HGNC Symbol;Acc:HGNC:19721]","synonyms":"SHAPY,SCAN-1","biotype":"protein_coding","ncbi_id":"124583","summary":"This protein encoded by this gene belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Mutations in this gene are associated with Desbuquois dysplasia with hand anomalies. Alternatively spliced transcript variants have been noted for this gene.[provided by RefSeq, Mar 2010]","start":78991717,"end":79009867,"strand":-1,"description":"calcium activated nucleotidase 1 [Source:HGNC Symbol;Acc:HGNC:19721]"}, {"versioned_ensembl_gene_id":"ENSG00000197580.11","gene_symbol":"BCO2","gene_name":"beta-carotene oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:18503]","synonyms":"B-DIOX-II,FLJ34464,BCDO2","biotype":"protein_coding","ncbi_id":"83875","summary":"This gene encodes an enzyme which oxidizes carotenoids such as beta-carotene during the biosynthesis of vitamin A. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":112175467,"end":112224699,"strand":1,"description":"beta-carotene oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:18503]"}, {"versioned_ensembl_gene_id":"ENSG00000137699.16","gene_symbol":"TRIM29","gene_name":"tripartite motif containing 29 [Source:HGNC Symbol;Acc:HGNC:17274]","synonyms":"FLJ36085,ATDC","biotype":"protein_coding","ncbi_id":"23650","summary":"The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype. [provided by RefSeq, Jul 2008]","start":120111275,"end":120185529,"strand":-1,"description":"tripartite motif containing 29 [Source:HGNC Symbol;Acc:HGNC:17274]"}, {"versioned_ensembl_gene_id":"ENSG00000263272.1","gene_symbol":"AC004148.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5425139,"end":5432876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231060.1","gene_symbol":"FARSBP1","gene_name":"phenylalanyl-tRNA synthetase beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45115]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647532","summary":null,"start":80776165,"end":80778088,"strand":-1,"description":"phenylalanyl-tRNA synthetase beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45115]"}, {"versioned_ensembl_gene_id":"ENSG00000107485.15","gene_symbol":"GATA3","gene_name":"GATA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4172]","synonyms":"HDR","biotype":"protein_coding","ncbi_id":"2625","summary":"This gene encodes a protein which belongs to the GATA family of transcription factors. The protein contains two GATA-type zinc fingers and is an important regulator of T-cell development and plays an important role in endothelial cell biology. Defects in this gene are the cause of hypoparathyroidism with sensorineural deafness and renal dysplasia. [provided by RefSeq, Nov 2009]","start":8053604,"end":8075198,"strand":1,"description":"GATA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4172]"}, {"versioned_ensembl_gene_id":"ENSG00000279570.1","gene_symbol":"AC099804.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78691266,"end":78691979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104888.9","gene_symbol":"SLC17A7","gene_name":"solute carrier family 17 member 7 [Source:HGNC Symbol;Acc:HGNC:16704]","synonyms":"VGLUT1,BNPI","biotype":"protein_coding","ncbi_id":"57030","summary":"The protein encoded by this gene is a vesicle-bound, sodium-dependent phosphate transporter that is specifically expressed in the neuron-rich regions of the brain. It is preferentially associated with the membranes of synaptic vesicles and functions in glutamate transport. The protein shares 82% identity with the differentiation-associated Na-dependent inorganic phosphate cotransporter and they appear to form a distinct class within the Na+/Pi cotransporter family. [provided by RefSeq, Jul 2008]","start":49429401,"end":49442360,"strand":-1,"description":"solute carrier family 17 member 7 [Source:HGNC Symbol;Acc:HGNC:16704]"}, {"versioned_ensembl_gene_id":"ENSG00000260193.1","gene_symbol":"AL138781.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136107808,"end":136109424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224032.6","gene_symbol":"EPB41L4A-AS1","gene_name":"EPB41L4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30749]","synonyms":"NCRNA00219,C5orf26,TIGA1","biotype":"lincRNA","ncbi_id":"114915","summary":null,"start":112160526,"end":112164276,"strand":1,"description":"EPB41L4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30749]"}, {"versioned_ensembl_gene_id":"ENSG00000254805.1","gene_symbol":"SNRPCP14","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49829]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310855","summary":null,"start":71690453,"end":71690657,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49829]"}, {"versioned_ensembl_gene_id":"ENSG00000254632.1","gene_symbol":"AP003119.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76759916,"end":76768223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254810.1","gene_symbol":"AP001189.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76654169,"end":76656712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242028.6","gene_symbol":"HYPK","gene_name":"huntingtin interacting protein K [Source:HGNC Symbol;Acc:HGNC:18418]","synonyms":"C15orf63,HSPC136,FLJ20431","biotype":"protein_coding","ncbi_id":"25764","summary":null,"start":43796142,"end":43803043,"strand":1,"description":"huntingtin interacting protein K [Source:HGNC Symbol;Acc:HGNC:18418]"}, {"versioned_ensembl_gene_id":"ENSG00000119326.14","gene_symbol":"CTNNAL1","gene_name":"catenin alpha like 1 [Source:HGNC Symbol;Acc:HGNC:2512]","synonyms":"CLLP,alpha-CATU","biotype":"protein_coding","ncbi_id":"8727","summary":null,"start":108942569,"end":109013529,"strand":-1,"description":"catenin alpha like 1 [Source:HGNC Symbol;Acc:HGNC:2512]"}, {"versioned_ensembl_gene_id":"ENSG00000253412.1","gene_symbol":"IGHVIII-13-1","gene_name":"immunoglobulin heavy variable (III)-13-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5693]","synonyms":"IGHV(III)-13-1","biotype":"IG_V_pseudogene","ncbi_id":"28351","summary":null,"start":106142287,"end":106142577,"strand":-1,"description":"immunoglobulin heavy variable (III)-13-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5693]"}, {"versioned_ensembl_gene_id":"ENSG00000036672.15","gene_symbol":"USP2","gene_name":"ubiquitin specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:12618]","synonyms":"UBP41","biotype":"protein_coding","ncbi_id":"9099","summary":"This gene encodes a member of the family of de-ubiquitinating enzymes, which belongs to the peptidase C19 superfamily. The encoded protein is a ubiquitin-specific protease which is required for TNF-alpha (tumor necrosis factor alpha) -induced NF-kB (nuclear factor kB) signaling. This protein deubiquitinates polyubiquitinated target proteins such as fatty acid synthase, murine double minute 2 (MDM2), MDM4/MDMX and cyclin D1. MDM2 and MDM4 are negative regulators of the p53 tumor suppressor and cyclin D1 is required for cell cycle G1/S transition. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":119355215,"end":119381726,"strand":-1,"description":"ubiquitin specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:12618]"}, {"versioned_ensembl_gene_id":"ENSG00000240051.1","gene_symbol":"RPL23AP10","gene_name":"ribosomal protein L23a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:19804]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326293","summary":null,"start":96456576,"end":96457041,"strand":-1,"description":"ribosomal protein L23a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:19804]"}, {"versioned_ensembl_gene_id":"ENSG00000090372.14","gene_symbol":"STRN4","gene_name":"striatin 4 [Source:HGNC Symbol;Acc:HGNC:15721]","synonyms":"ZIN,PPP2R6C","biotype":"protein_coding","ncbi_id":"29888","summary":null,"start":46719507,"end":46746994,"strand":-1,"description":"striatin 4 [Source:HGNC Symbol;Acc:HGNC:15721]"}, {"versioned_ensembl_gene_id":"ENSG00000076928.17","gene_symbol":"ARHGEF1","gene_name":"Rho guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:681]","synonyms":"SUB1.5,P115-RHOGEF,LBCL2","biotype":"protein_coding","ncbi_id":"9138","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form complex with G proteins and stimulate Rho-dependent signals. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]","start":41883161,"end":41930150,"strand":1,"description":"Rho guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:681]"}, {"versioned_ensembl_gene_id":"ENSG00000005700.14","gene_symbol":"IBTK","gene_name":"inhibitor of Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:17853]","synonyms":"DKFZP564B116,BTKI,BTBD26","biotype":"protein_coding","ncbi_id":"25998","summary":"Bruton tyrosine kinase (BTK) is a protein tyrosine kinase that is expressed in B cells, macrophages, and neutrophils. The protein encoded by this gene binds to BTK and downregulates BTK's kinase activity. In addition, the encoded protein disrupts BTK-mediated calcium mobilization and negatively regulates the activation of nuclear factor-kappa-B-driven transcription. This gene has a pseudogene on chromosome 18. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":82169983,"end":82247754,"strand":-1,"description":"inhibitor of Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:17853]"}, {"versioned_ensembl_gene_id":"ENSG00000130433.7","gene_symbol":"CACNG6","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 6 [Source:HGNC Symbol;Acc:HGNC:13625]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59285","summary":"Voltage-dependent calcium channels are composed of five subunits. The protein encoded by this gene represents one of these subunits, gamma, and is one of two known gamma subunit proteins. This particular gamma subunit is an integral membrane protein that is thought to stabilize the calcium channel in an inactive (closed) state. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members that function as transmembrane AMPA receptor regulatory proteins (TARPs). Alternative splicing results in multiple transcript variants. Variants in this gene have been associated with aspirin-intolerant asthma. [provided by RefSeq, Dec 2010]","start":53992288,"end":54012669,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 6 [Source:HGNC Symbol;Acc:HGNC:13625]"}, {"versioned_ensembl_gene_id":"ENSG00000181666.17","gene_symbol":"HKR1","gene_name":"HKR1, GLI-Kruppel zinc finger family member [Source:HGNC Symbol;Acc:HGNC:4928]","synonyms":"ZNF875","biotype":"protein_coding","ncbi_id":"284459","summary":null,"start":37312837,"end":37369365,"strand":1,"description":"HKR1, GLI-Kruppel zinc finger family member [Source:HGNC Symbol;Acc:HGNC:4928]"}, {"versioned_ensembl_gene_id":"ENSG00000180626.9","gene_symbol":"ZNF594","gene_name":"zinc finger protein 594 [Source:HGNC Symbol;Acc:HGNC:29392]","synonyms":"KIAA1871","biotype":"protein_coding","ncbi_id":"84622","summary":null,"start":5179536,"end":5191883,"strand":-1,"description":"zinc finger protein 594 [Source:HGNC Symbol;Acc:HGNC:29392]"}, {"versioned_ensembl_gene_id":"ENSG00000188295.14","gene_symbol":"ZNF669","gene_name":"zinc finger protein 669 [Source:HGNC Symbol;Acc:HGNC:25736]","synonyms":"FLJ12606","biotype":"protein_coding","ncbi_id":"79862","summary":null,"start":247099962,"end":247104372,"strand":-1,"description":"zinc finger protein 669 [Source:HGNC Symbol;Acc:HGNC:25736]"}, {"versioned_ensembl_gene_id":"ENSG00000214888.2","gene_symbol":"AL772337.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87857015,"end":87859399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227353.1","gene_symbol":"RAB28P3","gene_name":"RAB28, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50382]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132772","summary":null,"start":42492663,"end":42493570,"strand":1,"description":"RAB28, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50382]"}, {"versioned_ensembl_gene_id":"ENSG00000279324.1","gene_symbol":"AL645730.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49994318,"end":49996218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203387.2","gene_symbol":"AC074019.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":228352120,"end":228353215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258935.1","gene_symbol":"AL096869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90567495,"end":90569976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134780.9","gene_symbol":"DAGLA","gene_name":"diacylglycerol lipase alpha [Source:HGNC Symbol;Acc:HGNC:1165]","synonyms":"NSDDR,KIAA0659,DAGLALPHA,C11orf11","biotype":"protein_coding","ncbi_id":"747","summary":"This gene encodes a diacylglycerol lipase. The encoded enzyme is involved in the biosynthesis of the endocannabinoid 2-arachidonoyl-glycerol.[provided by RefSeq, Nov 2010]","start":61680433,"end":61747001,"strand":1,"description":"diacylglycerol lipase alpha [Source:HGNC Symbol;Acc:HGNC:1165]"}, {"versioned_ensembl_gene_id":"ENSG00000277260.1","gene_symbol":"FAM74A7","gene_name":"family with sequence similarity 74 member A7 [Source:HGNC Symbol;Acc:HGNC:34037]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996582","summary":null,"start":42199000,"end":42204988,"strand":1,"description":"family with sequence similarity 74 member A7 [Source:HGNC Symbol;Acc:HGNC:34037]"}, {"versioned_ensembl_gene_id":"ENSG00000131730.15","gene_symbol":"CKMT2","gene_name":"creatine kinase, mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:1996]","synonyms":"SMTCK","biotype":"protein_coding","ncbi_id":"1160","summary":"Mitochondrial creatine kinase (MtCK) is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine. It belongs to the creatine kinase isoenzyme family. It exists as two isoenzymes, sarcomeric MtCK and ubiquitous MtCK, encoded by separate genes. Mitochondrial creatine kinase occurs in two different oligomeric forms: dimers and octamers, in contrast to the exclusively dimeric cytosolic creatine kinase isoenzymes. Sarcomeric mitochondrial creatine kinase has 80% homology with the coding exons of ubiquitous mitochondrial creatine kinase. This gene contains sequences homologous to several motifs that are shared among some nuclear genes encoding mitochondrial proteins and thus may be essential for the coordinated activation of these genes during mitochondrial biogenesis. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":81233285,"end":81266397,"strand":1,"description":"creatine kinase, mitochondrial 2 [Source:HGNC Symbol;Acc:HGNC:1996]"}, {"versioned_ensembl_gene_id":"ENSG00000177889.9","gene_symbol":"UBE2N","gene_name":"ubiquitin conjugating enzyme E2 N [Source:HGNC Symbol;Acc:HGNC:12492]","synonyms":"UbcH-ben,UBC13,MGC8489","biotype":"protein_coding","ncbi_id":"7334","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. Studies in mouse suggest that this protein plays a role in DNA postreplication repair. [provided by RefSeq, Jul 2008]","start":93405673,"end":93442262,"strand":-1,"description":"ubiquitin conjugating enzyme E2 N [Source:HGNC Symbol;Acc:HGNC:12492]"}, {"versioned_ensembl_gene_id":"ENSG00000270578.1","gene_symbol":"AP000787.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95145437,"end":95146004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186868.15","gene_symbol":"MAPT","gene_name":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]","synonyms":"PPP1R103,MAPTL,PPND,FTDP-17,MTBT2,FLJ31424,MTBT1,DDPAC,MSTD,tau,MGC138549","biotype":"protein_coding","ncbi_id":"4137","summary":"This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008]","start":45894382,"end":46028334,"strand":1,"description":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]"}, {"versioned_ensembl_gene_id":"ENSG00000263465.4","gene_symbol":"SRSF8","gene_name":"serine and arginine rich splicing factor 8 [Source:HGNC Symbol;Acc:HGNC:16988]","synonyms":"SRP46,SFRS2B","biotype":"protein_coding","ncbi_id":"10929","summary":"This gene encodes a member of a family of proteins containing a ribonucleoprotein (RNP)-type RNA binding motif and a carboxyl-terminal arginine-serine-rich (RS) domain. The encoded protein functions as a pre-mRNA splicing factor. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":95067197,"end":95071224,"strand":1,"description":"serine and arginine rich splicing factor 8 [Source:HGNC Symbol;Acc:HGNC:16988]"}, {"versioned_ensembl_gene_id":"ENSG00000248676.1","gene_symbol":"AC083902.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99594799,"end":99625913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095059.15","gene_symbol":"DHPS","gene_name":"deoxyhypusine synthase [Source:HGNC Symbol;Acc:HGNC:2869]","synonyms":"MIG13","biotype":"protein_coding","ncbi_id":"1725","summary":"This gene encodes a protein that is required for the formation of hypusine, a unique amino acid formed by the posttranslational modification of only one protein, eukaryotic translation initiation factor 5A. The encoded protein catalyzes the first step in hypusine formation by transferring the butylamine moiety of spermidine to a specific lysine residue of the eukaryotic translation initiation factor 5A precursor, forming an intermediate deoxyhypusine residue. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2011]","start":12675717,"end":12681902,"strand":-1,"description":"deoxyhypusine synthase [Source:HGNC Symbol;Acc:HGNC:2869]"}, {"versioned_ensembl_gene_id":"ENSG00000197472.14","gene_symbol":"ZNF695","gene_name":"zinc finger protein 695 [Source:HGNC Symbol;Acc:HGNC:30954]","synonyms":"SBZF3","biotype":"protein_coding","ncbi_id":"57116","summary":null,"start":246945547,"end":247008093,"strand":-1,"description":"zinc finger protein 695 [Source:HGNC Symbol;Acc:HGNC:30954]"}, {"versioned_ensembl_gene_id":"ENSG00000138823.13","gene_symbol":"MTTP","gene_name":"microsomal triglyceride transfer protein [Source:HGNC Symbol;Acc:HGNC:7467]","synonyms":"MTP,ABL","biotype":"protein_coding","ncbi_id":"4547","summary":"MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia. [provided by RefSeq, Jul 2008]","start":99563761,"end":99623999,"strand":1,"description":"microsomal triglyceride transfer protein [Source:HGNC Symbol;Acc:HGNC:7467]"}, {"versioned_ensembl_gene_id":"ENSG00000277462.1","gene_symbol":"ZNF670","gene_name":"zinc finger protein 670 [Source:HGNC Symbol;Acc:HGNC:28167]","synonyms":"MGC12466","biotype":"protein_coding","ncbi_id":"93474","summary":null,"start":247036784,"end":247078755,"strand":-1,"description":"zinc finger protein 670 [Source:HGNC Symbol;Acc:HGNC:28167]"}, {"versioned_ensembl_gene_id":"ENSG00000233208.5","gene_symbol":"LINC00642","gene_name":"long intergenic non-protein coding RNA 642 [Source:HGNC Symbol;Acc:HGNC:44293]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400238","summary":null,"start":90455230,"end":90458905,"strand":1,"description":"long intergenic non-protein coding RNA 642 [Source:HGNC Symbol;Acc:HGNC:44293]"}, {"versioned_ensembl_gene_id":"ENSG00000176343.5","gene_symbol":"RPL37AP8","gene_name":"ribosomal protein L37a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35645]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644338","summary":null,"start":111889199,"end":111889474,"strand":-1,"description":"ribosomal protein L37a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35645]"}, {"versioned_ensembl_gene_id":"ENSG00000258734.2","gene_symbol":"AL049873.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58827679,"end":58828176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213598.4","gene_symbol":"AL049873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58794654,"end":58795029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136155.16","gene_symbol":"SCEL","gene_name":"sciellin [Source:HGNC Symbol;Acc:HGNC:10573]","synonyms":"MGC22531,FLJ21667","biotype":"protein_coding","ncbi_id":"8796","summary":"The protein encoded by this gene is a precursor to the cornified envelope of terminally differentiated keratinocytes. This protein localizes to the periphery of cells and may function in the assembly or regulation of proteins in the cornified envelope. Transcript variants encoding different isoforms exist. A transcript variant utilizing an alternative polyA signal has been described in the literature, but its full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":77535674,"end":77645263,"strand":1,"description":"sciellin [Source:HGNC Symbol;Acc:HGNC:10573]"}, {"versioned_ensembl_gene_id":"ENSG00000232888.4","gene_symbol":"AC127070.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132825701,"end":132826184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224347.6","gene_symbol":"SCEL-AS1","gene_name":"SCEL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39895]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355296","summary":null,"start":77599755,"end":77606551,"strand":-1,"description":"SCEL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39895]"}, {"versioned_ensembl_gene_id":"ENSG00000250544.1","gene_symbol":"LINC02059","gene_name":"long intergenic non-protein coding RNA 2059 [Source:HGNC Symbol;Acc:HGNC:52902]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505878","summary":null,"start":86746818,"end":86749772,"strand":1,"description":"long intergenic non-protein coding RNA 2059 [Source:HGNC Symbol;Acc:HGNC:52902]"}, {"versioned_ensembl_gene_id":"ENSG00000214211.2","gene_symbol":"CTAGE14P","gene_name":"CTAGE family member 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:37299]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401018","summary":null,"start":167713663,"end":167716065,"strand":-1,"description":"CTAGE family member 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:37299]"}, {"versioned_ensembl_gene_id":"ENSG00000117481.10","gene_symbol":"NSUN4","gene_name":"NOP2/Sun RNA methyltransferase family member 4 [Source:HGNC Symbol;Acc:HGNC:31802]","synonyms":"SHTAP,MGC22960","biotype":"protein_coding","ncbi_id":"387338","summary":null,"start":46340177,"end":46365152,"strand":1,"description":"NOP2/Sun RNA methyltransferase family member 4 [Source:HGNC Symbol;Acc:HGNC:31802]"}, {"versioned_ensembl_gene_id":"ENSG00000090615.14","gene_symbol":"GOLGA3","gene_name":"golgin A3 [Source:HGNC Symbol;Acc:HGNC:4426]","synonyms":"MEA-2,golgin-160,GCP170","biotype":"protein_coding","ncbi_id":"2802","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes a member of the golgin family of proteins which are localized to the Golgi. Its encoded protein has been postulated to play a role in nuclear transport and Golgi apparatus localization. Several alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Feb 2010]","start":132768909,"end":132828858,"strand":-1,"description":"golgin A3 [Source:HGNC Symbol;Acc:HGNC:4426]"}, {"versioned_ensembl_gene_id":"ENSG00000227051.6","gene_symbol":"C14orf132","gene_name":"chromosome 14 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:20346]","synonyms":"C14orf88","biotype":"protein_coding","ncbi_id":"56967","summary":null,"start":96039324,"end":96093889,"strand":1,"description":"chromosome 14 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:20346]"}, {"versioned_ensembl_gene_id":"ENSG00000260541.1","gene_symbol":"AL031722.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":1841020,"end":1843547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214425.7","gene_symbol":"LRRC37A4P","gene_name":"leucine rich repeat containing 37 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:25479]","synonyms":"LRRC37A4,FLJ10120","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"55073","summary":null,"start":45506741,"end":45550335,"strand":-1,"description":"leucine rich repeat containing 37 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:25479]"}, {"versioned_ensembl_gene_id":"ENSG00000196967.10","gene_symbol":"ZNF585A","gene_name":"zinc finger protein 585A [Source:HGNC Symbol;Acc:HGNC:26305]","synonyms":"FLJ23765","biotype":"protein_coding","ncbi_id":"199704","summary":null,"start":37106734,"end":37172741,"strand":-1,"description":"zinc finger protein 585A [Source:HGNC Symbol;Acc:HGNC:26305]"}, {"versioned_ensembl_gene_id":"ENSG00000227859.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29474898,"end":29475944,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000258100.1","gene_symbol":"AC025035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91362196,"end":91368606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137869.14","gene_symbol":"CYP19A1","gene_name":"cytochrome P450 family 19 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2594]","synonyms":"P-450AROM,CYP19,CYAR,CPV1,aromatase,ARO1,ARO","biotype":"protein_coding","ncbi_id":"1588","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and catalyzes the last steps of estrogen biosynthesis. Mutations in this gene can result in either increased or decreased aromatase activity; the associated phenotypes suggest that estrogen functions both as a sex steroid hormone and in growth or differentiation. Alternative promoter use and alternative splicing results in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]","start":51208057,"end":51338610,"strand":-1,"description":"cytochrome P450 family 19 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2594]"}, {"versioned_ensembl_gene_id":"ENSG00000168661.14","gene_symbol":"ZNF30","gene_name":"zinc finger protein 30 [Source:HGNC Symbol;Acc:HGNC:13090]","synonyms":"KOX28,FLJ20562,DKFZp686N19164","biotype":"protein_coding","ncbi_id":"90075","summary":null,"start":34926903,"end":34945170,"strand":1,"description":"zinc finger protein 30 [Source:HGNC Symbol;Acc:HGNC:13090]"}, {"versioned_ensembl_gene_id":"ENSG00000223519.8","gene_symbol":"KIF28P","gene_name":"kinesin family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:49205]","synonyms":"KLP-6","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100130097","summary":null,"start":246771837,"end":246839611,"strand":-1,"description":"kinesin family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:49205]"}, {"versioned_ensembl_gene_id":"ENSG00000227953.6","gene_symbol":"LINC01341","gene_name":"long intergenic non-protein coding RNA 1341 [Source:HGNC Symbol;Acc:HGNC:49457]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"149134","summary":null,"start":246776013,"end":246792385,"strand":1,"description":"long intergenic non-protein coding RNA 1341 [Source:HGNC Symbol;Acc:HGNC:49457]"}, {"versioned_ensembl_gene_id":"ENSG00000260855.1","gene_symbol":"AL591848.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":246772301,"end":246775772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235386.1","gene_symbol":"AC113174.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246818076,"end":246818180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270624.1","gene_symbol":"AC008555.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34866352,"end":34866919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233536.2","gene_symbol":"AP000943.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94638038,"end":94640833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283906.1","gene_symbol":"ABBA01040607.1","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106872783,"end":106873186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266311.6","gene_symbol":"AC007952.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19164209,"end":19174436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211976.2","gene_symbol":"IGHV3-73","gene_name":"immunoglobulin heavy variable 3-73 [Source:HGNC Symbol;Acc:HGNC:5623]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28409","summary":null,"start":106802694,"end":106803233,"strand":-1,"description":"immunoglobulin heavy variable 3-73 [Source:HGNC Symbol;Acc:HGNC:5623]"}, {"versioned_ensembl_gene_id":"ENSG00000253247.1","gene_symbol":"IGHV3-76","gene_name":"immunoglobulin heavy variable 3-76 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5626]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28406","summary":null,"start":106827869,"end":106828163,"strand":-1,"description":"immunoglobulin heavy variable 3-76 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5626]"}, {"versioned_ensembl_gene_id":"ENSG00000154079.5","gene_symbol":"SDHAF4","gene_name":"succinate dehydrogenase complex assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:20957]","synonyms":"C6orf57,Sdh8","biotype":"protein_coding","ncbi_id":"135154","summary":null,"start":70566917,"end":70589569,"strand":1,"description":"succinate dehydrogenase complex assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:20957]"}, {"versioned_ensembl_gene_id":"ENSG00000261863.1","gene_symbol":"LINC01996","gene_name":"long intergenic non-protein coding RNA 1996 [Source:HGNC Symbol;Acc:HGNC:52830]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400568","summary":null,"start":4610449,"end":4617650,"strand":1,"description":"long intergenic non-protein coding RNA 1996 [Source:HGNC Symbol;Acc:HGNC:52830]"}, {"versioned_ensembl_gene_id":"ENSG00000276258.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"CD158J,cl-49,nkat5,183ActI","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738568,"end":54752475,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000245598.6","gene_symbol":"DACT3-AS1","gene_name":"DACT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44120]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506068","summary":null,"start":46660364,"end":46677447,"strand":1,"description":"DACT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44120]"}, {"versioned_ensembl_gene_id":"ENSG00000167741.10","gene_symbol":"GGT6","gene_name":"gamma-glutamyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:26891]","synonyms":"FLJ90165","biotype":"protein_coding","ncbi_id":"124975","summary":"GGT6 belongs to the gamma-glutamyltransferase (GGT; EC 2.3.2.2) gene family. GGT is a membrane-bound extracellular enzyme that cleaves gamma-glutamyl peptide bonds in glutathione and other peptides and transfers the gamma-glutamyl moiety to acceptors. GGT is also key to glutathione homeostasis because it provides substrates for glutathione synthesis (Heisterkamp et al., 2008 [PubMed 18357469]).[supplied by OMIM, Oct 2008]","start":4556927,"end":4560818,"strand":-1,"description":"gamma-glutamyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:26891]"}, {"versioned_ensembl_gene_id":"ENSG00000235298.1","gene_symbol":"AL354733.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83972233,"end":83975777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278971.1","gene_symbol":"AC091305.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70489630,"end":70491205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227703.4","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30475795,"end":30476445,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000223412.3","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"Em:AB014080.4,SUCLA2P","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30458739,"end":30460108,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000237207.2","gene_symbol":"RBM17P3","gene_name":"RNA binding motif protein 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132949","summary":null,"start":41974362,"end":41975768,"strand":1,"description":"RNA binding motif protein 17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50368]"}, {"versioned_ensembl_gene_id":"ENSG00000225672.1","gene_symbol":"CCNT2P1","gene_name":"cyclin T2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39178]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418763","summary":null,"start":111007700,"end":111015530,"strand":-1,"description":"cyclin T2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39178]"}, {"versioned_ensembl_gene_id":"ENSG00000211938.2","gene_symbol":"IGHV3-7","gene_name":"immunoglobulin heavy variable 3-7 [Source:HGNC Symbol;Acc:HGNC:5620]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28452","summary":null,"start":106062151,"end":106062683,"strand":-1,"description":"immunoglobulin heavy variable 3-7 [Source:HGNC Symbol;Acc:HGNC:5620]"}, {"versioned_ensembl_gene_id":"ENSG00000258148.2","gene_symbol":"AC007115.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91193709,"end":91193942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253763.1","gene_symbol":"IGHV3-6","gene_name":"immunoglobulin heavy variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5613]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28453","summary":null,"start":106055549,"end":106055998,"strand":-1,"description":"immunoglobulin heavy variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5613]"}, {"versioned_ensembl_gene_id":"ENSG00000271373.1","gene_symbol":"NANOGP3","gene_name":"Nanog homeobox pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23101]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340217","summary":null,"start":53418452,"end":53418737,"strand":-1,"description":"Nanog homeobox pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23101]"}, {"versioned_ensembl_gene_id":"ENSG00000274189.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54848193,"end":54859216,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000234258.6","gene_symbol":"HSPA1L","gene_name":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]","synonyms":"hum70t,HSP70-HOM","biotype":"protein_coding","ncbi_id":"3305","summary":"This gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein. [provided by RefSeq, Jul 2008]","start":31791805,"end":31797251,"strand":-1,"description":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]"}, {"versioned_ensembl_gene_id":"ENSG00000229629.1","gene_symbol":"AL500527.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102089968,"end":102090062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267546.2","gene_symbol":"AC015802.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76545668,"end":76557683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228879.1","gene_symbol":"AL591848.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":246755511,"end":246755832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274861.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000242858.1","gene_symbol":"AC020899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83746388,"end":83746989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251456.1","gene_symbol":"AC113398.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":124734618,"end":124735175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164404.8","gene_symbol":"GDF9","gene_name":"growth differentiation factor 9 [Source:HGNC Symbol;Acc:HGNC:4224]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2661","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates ovarian function. Reduced expression of this gene may be associated with polycystic ovary syndrome and mutations in this gene may be more common in mothers of dizygotic twins. [provided by RefSeq, Jul 2016]","start":132861181,"end":132866884,"strand":-1,"description":"growth differentiation factor 9 [Source:HGNC Symbol;Acc:HGNC:4224]"}, {"versioned_ensembl_gene_id":"ENSG00000267446.1","gene_symbol":"AC003070.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45371402,"end":45372057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242852.6","gene_symbol":"ZNF709","gene_name":"zinc finger protein 709 [Source:HGNC Symbol;Acc:HGNC:20629]","synonyms":"FLJ38281","biotype":"protein_coding","ncbi_id":"163051","summary":null,"start":12461184,"end":12513854,"strand":-1,"description":"zinc finger protein 709 [Source:HGNC Symbol;Acc:HGNC:20629]"}, {"versioned_ensembl_gene_id":"ENSG00000129654.7","gene_symbol":"FOXJ1","gene_name":"forkhead box J1 [Source:HGNC Symbol;Acc:HGNC:3816]","synonyms":"FKHL13,HFH4,HFH-4","biotype":"protein_coding","ncbi_id":"2302","summary":"This gene encodes a member of the forkhead family of transcription factors. Similar genes in zebrafish and mouse have been shown to regulate the transcription of genes that control the production of motile cilia. The mouse ortholog also functions in the determination of left-right asymmetry. Polymorphisms in this gene are associated with systemic lupus erythematosus and allergic rhinitis.[provided by RefSeq, Sep 2009]","start":76136333,"end":76141299,"strand":-1,"description":"forkhead box J1 [Source:HGNC Symbol;Acc:HGNC:3816]"}, {"versioned_ensembl_gene_id":"ENSG00000232811.1","gene_symbol":"AL360270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110943467,"end":110952848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121931.15","gene_symbol":"LRIF1","gene_name":"ligand dependent nuclear receptor interacting factor 1 [Source:HGNC Symbol;Acc:HGNC:30299]","synonyms":"FLJ11269,C1orf103,RIF1","biotype":"protein_coding","ncbi_id":"55791","summary":null,"start":110947185,"end":110964079,"strand":-1,"description":"ligand dependent nuclear receptor interacting factor 1 [Source:HGNC Symbol;Acc:HGNC:30299]"}, {"versioned_ensembl_gene_id":"ENSG00000258390.1","gene_symbol":"LINC02318","gene_name":"long intergenic non-protein coding RNA 2318 [Source:HGNC Symbol;Acc:HGNC:53237]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506999","summary":null,"start":95573562,"end":95581956,"strand":1,"description":"long intergenic non-protein coding RNA 2318 [Source:HGNC Symbol;Acc:HGNC:53237]"}, {"versioned_ensembl_gene_id":"ENSG00000267376.1","gene_symbol":"AC015801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76202644,"end":76202796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239568.1","gene_symbol":"AC104435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72583370,"end":72583535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105388.15","gene_symbol":"CEACAM5","gene_name":"carcinoembryonic antigen related cell adhesion molecule 5 [Source:HGNC Symbol;Acc:HGNC:1817]","synonyms":"CEA,CD66e","biotype":"protein_coding","ncbi_id":"1048","summary":"This gene encodes a cell surface glycoprotein that represents the founding member of the carcinoembryonic antigen (CEA) family of proteins. The encoded protein is used as a clinical biomarker for gastrointestinal cancers and may promote tumor development through its role as a cell adhesion molecule. Additionally, the encoded protein may regulate differentiation, apoptosis, and cell polarity. This gene is present in a CEA family gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":41708585,"end":41729798,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 5 [Source:HGNC Symbol;Acc:HGNC:1817]"}, {"versioned_ensembl_gene_id":"ENSG00000223672.2","gene_symbol":"AL162386.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13322806,"end":13323450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227913.1","gene_symbol":"KRT8P44","gene_name":"keratin 8 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:39878]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129958","summary":null,"start":162568379,"end":162569728,"strand":1,"description":"keratin 8 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:39878]"}, {"versioned_ensembl_gene_id":"ENSG00000270816.5","gene_symbol":"LINC00221","gene_name":"long intergenic non-protein coding RNA 221 [Source:HGNC Symbol;Acc:HGNC:20169]","synonyms":"NCRNA00221,C14orf98","biotype":"lincRNA","ncbi_id":"338005","summary":null,"start":106482439,"end":106521073,"strand":1,"description":"long intergenic non-protein coding RNA 221 [Source:HGNC Symbol;Acc:HGNC:20169]"}, {"versioned_ensembl_gene_id":"ENSG00000276502.1","gene_symbol":"AL354718.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41310816,"end":41332962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254004.6","gene_symbol":"ZNF260","gene_name":"zinc finger protein 260 [Source:HGNC Symbol;Acc:HGNC:13499]","synonyms":"Zfp260,ozrf1","biotype":"protein_coding","ncbi_id":"339324","summary":null,"start":36510695,"end":36528660,"strand":-1,"description":"zinc finger protein 260 [Source:HGNC Symbol;Acc:HGNC:13499]"}, {"versioned_ensembl_gene_id":"ENSG00000197497.10","gene_symbol":"ZNF665","gene_name":"zinc finger protein 665 [Source:HGNC Symbol;Acc:HGNC:25885]","synonyms":"FLJ14345","biotype":"protein_coding","ncbi_id":"79788","summary":null,"start":53159213,"end":53193386,"strand":-1,"description":"zinc finger protein 665 [Source:HGNC Symbol;Acc:HGNC:25885]"}, {"versioned_ensembl_gene_id":"ENSG00000267788.1","gene_symbol":"AC015936.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44982514,"end":44982772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164022.16","gene_symbol":"AIMP1","gene_name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 [Source:HGNC Symbol;Acc:HGNC:10648]","synonyms":"p43,EMAPII,EMAP-2,SCYE1","biotype":"protein_coding","ncbi_id":"9255","summary":"The protein encoded by this gene is a cytokine that is specifically induced by apoptosis, and it is involved in the control of angiogenesis, inflammation, and wound healing. The release of this cytokine renders the tumor-associated vasculature sensitive to tumor necrosis factor. The precursor protein is identical to the p43 subunit, which is associated with the multi-tRNA synthetase complex, and it modulates aminoacylation activity of tRNA synthetase in normal cells. This protein is also involved in the stimulation of inflammatory responses after proteolytic cleavage in tumor cells. Multiple transcript variants encoding different isoforms have been found for this gene. A pseudogene has been identified on chromosome 20. [provided by RefSeq, Dec 2008]","start":106315544,"end":106349226,"strand":1,"description":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 [Source:HGNC Symbol;Acc:HGNC:10648]"}, {"versioned_ensembl_gene_id":"ENSG00000276831.1","gene_symbol":"AC020922.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55338945,"end":55339283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254932.2","gene_symbol":"AP001007.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125258626,"end":125266798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239281.2","gene_symbol":"RPS29P2","gene_name":"ribosomal protein S29 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31083]","synonyms":"HsT23291","biotype":"processed_pseudogene","ncbi_id":"619452","summary":null,"start":41271431,"end":41271566,"strand":1,"description":"ribosomal protein S29 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31083]"}, {"versioned_ensembl_gene_id":"ENSG00000104332.11","gene_symbol":"SFRP1","gene_name":"secreted frizzled related protein 1 [Source:HGNC Symbol;Acc:HGNC:10776]","synonyms":"FRP-1,FRP,SARP2","biotype":"protein_coding","ncbi_id":"6422","summary":"This gene encodes a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins. Members of this family act as soluble modulators of Wnt signaling; epigenetic silencing of SFRP genes leads to deregulated activation of the Wnt-pathway which is associated with cancer. This gene may also be involved in determining the polarity of photoreceptor cells in the retina. [provided by RefSeq, Sep 2009]","start":41261958,"end":41309497,"strand":-1,"description":"secreted frizzled related protein 1 [Source:HGNC Symbol;Acc:HGNC:10776]"}, {"versioned_ensembl_gene_id":"ENSG00000015413.9","gene_symbol":"DPEP1","gene_name":"dipeptidase 1 (renal) [Source:HGNC Symbol;Acc:HGNC:3002]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1800","summary":"The protein encoded by this gene is a kidney membrane enzyme involved in the metabolism of glutathione and other similar proteins by dipeptide hydrolysis. The encoded protein is known to regulate leukotriene activity by catalyzing the conversion of leukotriene D4 to leukotriene E4. This protein uses zinc as a cofactor and acts as a disulfide-linked homodimer. [provided by RefSeq, Dec 2020]","start":89613308,"end":89638456,"strand":1,"description":"dipeptidase 1 (renal) [Source:HGNC Symbol;Acc:HGNC:3002]"}, {"versioned_ensembl_gene_id":"ENSG00000279329.1","gene_symbol":"AC020910.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34675717,"end":34677581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165495.15","gene_symbol":"PKNOX2","gene_name":"PBX/knotted 1 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:16714]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63876","summary":"Homeodomain proteins are sequence-specific transcription factors that share a highly conserved DNA-binding domain and play fundamental roles in cell proliferation, differentiation, and death. PKNOX2 belongs to the TALE (3-amino acid loop extension) class of homeodomain proteins characterized by a 3-amino acid extension between alpha helices 1 and 2 within the homeodomain (Imoto et al., 2001 [PubMed 11549286]).[supplied by OMIM, Oct 2009]","start":125164687,"end":125433389,"strand":1,"description":"PBX/knotted 1 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:16714]"}, {"versioned_ensembl_gene_id":"ENSG00000187398.11","gene_symbol":"LUZP2","gene_name":"leucine zipper protein 2 [Source:HGNC Symbol;Acc:HGNC:23206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338645","summary":"This gene encodes a leucine zipper protein. This protein is deleted in some patients with Wilms tumor-Aniridia-Genitourinary anomalies-mental Retardation (WAGR) syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":24496970,"end":25082631,"strand":1,"description":"leucine zipper protein 2 [Source:HGNC Symbol;Acc:HGNC:23206]"}, {"versioned_ensembl_gene_id":"ENSG00000139645.9","gene_symbol":"ANKRD52","gene_name":"ankyrin repeat domain 52 [Source:HGNC Symbol;Acc:HGNC:26614]","synonyms":"PP6-ARS-C,FLJ34236","biotype":"protein_coding","ncbi_id":"283373","summary":null,"start":56237807,"end":56258391,"strand":-1,"description":"ankyrin repeat domain 52 [Source:HGNC Symbol;Acc:HGNC:26614]"}, {"versioned_ensembl_gene_id":"ENSG00000278744.1","gene_symbol":"AL449363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134009033,"end":134009218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283307.1","gene_symbol":"OR5AK4P","gene_name":"olfactory receptor family 5 subfamily AK member 4 pseudogene [Source:NCBI gene;Acc:219525]","synonyms":"PJCG3","biotype":"unprocessed_pseudogene","ncbi_id":"219525","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57037534,"end":57038436,"strand":1,"description":"olfactory receptor family 5 subfamily AK member 4 pseudogene [Source:NCBI gene;Acc:219525]"}, {"versioned_ensembl_gene_id":"ENSG00000237845.1","gene_symbol":"AL139161.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235942553,"end":235943805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101278.6","gene_symbol":"RPS10P5","gene_name":"ribosomal protein S10 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15795]","synonyms":"bA371L19.2,RPS10L","biotype":"processed_pseudogene","ncbi_id":"93144","summary":null,"start":839447,"end":839977,"strand":-1,"description":"ribosomal protein S10 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:15795]"}, {"versioned_ensembl_gene_id":"ENSG00000170584.10","gene_symbol":"NUDCD2","gene_name":"NudC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30535]","synonyms":"NudCL2,DKFZp686E10109","biotype":"protein_coding","ncbi_id":"134492","summary":null,"start":163446526,"end":163460140,"strand":-1,"description":"NudC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30535]"}, {"versioned_ensembl_gene_id":"ENSG00000262482.1","gene_symbol":"AC004034.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2939714,"end":2954276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262959.2","gene_symbol":"RPL23AP86","gene_name":"ribosomal protein L23a pseudogene 86 [Source:HGNC Symbol;Acc:HGNC:51577]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507357","summary":null,"start":2922662,"end":2923202,"strand":-1,"description":"ribosomal protein L23a pseudogene 86 [Source:HGNC Symbol;Acc:HGNC:51577]"}, {"versioned_ensembl_gene_id":"ENSG00000018280.16","gene_symbol":"SLC11A1","gene_name":"solute carrier family 11 member 1 [Source:HGNC Symbol;Acc:HGNC:10907]","synonyms":"NRAMP1,NRAMP,LSH","biotype":"protein_coding","ncbi_id":"6556","summary":"This gene is a member of the solute carrier family 11 (proton-coupled divalent metal ion transporters) family and encodes a multi-pass membrane protein. The protein functions as a divalent transition metal (iron and manganese) transporter involved in iron metabolism and host resistance to certain pathogens. Mutations in this gene have been associated with susceptibility to infectious diseases such as tuberculosis and leprosy, and inflammatory diseases such as rheumatoid arthritis and Crohn disease. Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]","start":218382029,"end":218396894,"strand":1,"description":"solute carrier family 11 member 1 [Source:HGNC Symbol;Acc:HGNC:10907]"}, {"versioned_ensembl_gene_id":"ENSG00000250114.1","gene_symbol":"AC008723.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":163416525,"end":163416731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168876.8","gene_symbol":"ANKRD49","gene_name":"ankyrin repeat domain 49 [Source:HGNC Symbol;Acc:HGNC:25970]","synonyms":"GBIF,FLJ20189,FGIF","biotype":"protein_coding","ncbi_id":"54851","summary":null,"start":94493629,"end":94499583,"strand":1,"description":"ankyrin repeat domain 49 [Source:HGNC Symbol;Acc:HGNC:25970]"}, {"versioned_ensembl_gene_id":"ENSG00000232555.1","gene_symbol":"AC104088.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":172315287,"end":172323737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253842.1","gene_symbol":"AP003472.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100428834,"end":100430997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257379.1","gene_symbol":"AC023509.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":53441741,"end":53467528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250509.1","gene_symbol":"AC034213.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180441559,"end":180443238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224389.8","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"CO4,C4B3,CH,C4B1,CPAMD3,C4F","biotype":"protein_coding","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":32014762,"end":32035418,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000235768.1","gene_symbol":"BRD7P5","gene_name":"bromodomain containing 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129259","summary":null,"start":94757451,"end":94759272,"strand":-1,"description":"bromodomain containing 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37631]"}, {"versioned_ensembl_gene_id":"ENSG00000173991.5","gene_symbol":"TCAP","gene_name":"titin-cap [Source:HGNC Symbol;Acc:HGNC:11610]","synonyms":"TELE,T-cap,LGMD2G,CMD1N,telethonin","biotype":"protein_coding","ncbi_id":"8557","summary":"Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G. [provided by RefSeq, Jul 2008]","start":39664187,"end":39666555,"strand":1,"description":"titin-cap [Source:HGNC Symbol;Acc:HGNC:11610]"}, {"versioned_ensembl_gene_id":"ENSG00000280157.1","gene_symbol":"AL359510.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":228121523,"end":228123771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253587.2","gene_symbol":"IGHV3-30-2","gene_name":"immunoglobulin heavy variable 3-30-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5592]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28438","summary":null,"start":106344385,"end":106344833,"strand":-1,"description":"immunoglobulin heavy variable 3-30-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5592]"}, {"versioned_ensembl_gene_id":"ENSG00000237424.1","gene_symbol":"FOXD2-AS1","gene_name":"FOXD2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44256]","synonyms":"MGC12982","biotype":"antisense_RNA","ncbi_id":"84793","summary":null,"start":47432133,"end":47434641,"strand":-1,"description":"FOXD2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44256]"}, {"versioned_ensembl_gene_id":"ENSG00000150401.14","gene_symbol":"DCUN1D2","gene_name":"defective in cullin neddylation 1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20328]","synonyms":"C13orf17,FLJ20092,FLJ10704","biotype":"protein_coding","ncbi_id":"55208","summary":null,"start":113455819,"end":113490952,"strand":-1,"description":"defective in cullin neddylation 1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20328]"}, {"versioned_ensembl_gene_id":"ENSG00000119383.19","gene_symbol":"PTPA","gene_name":"protein phosphatase 2 phosphatase activator [Source:HGNC Symbol;Acc:HGNC:9308]","synonyms":"PR53,PPP2R4","biotype":"protein_coding","ncbi_id":"5524","summary":"Protein phosphatase 2A is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phosphatase 2A holoenzymes are heterotrimeric proteins composed of a structural subunit A, a catalytic subunit C, and a regulatory subunit B. The regulatory subunit is encoded by a diverse set of genes that have been grouped into the B/PR55, B'/PR61, and B''/PR72 families. These different regulatory subunits confer distinct enzymatic specificities and intracellular localizations to the holozenzyme. The product of this gene belongs to the B' family. This gene encodes a specific phosphotyrosyl phosphatase activator of the dimeric form of protein phosphatase 2A. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":129110950,"end":129148946,"strand":1,"description":"protein phosphatase 2 phosphatase activator [Source:HGNC Symbol;Acc:HGNC:9308]"}, {"versioned_ensembl_gene_id":"ENSG00000273674.4","gene_symbol":"AC021752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50839875,"end":50908599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242412.1","gene_symbol":"DBIL5P2","gene_name":"diazepam binding inhibitor-like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38518]","synonyms":"ELP1P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100169989","summary":null,"start":63117851,"end":63119542,"strand":-1,"description":"diazepam binding inhibitor-like 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38518]"}, {"versioned_ensembl_gene_id":"ENSG00000102189.16","gene_symbol":"EEA1","gene_name":"early endosome antigen 1 [Source:HGNC Symbol;Acc:HGNC:3185]","synonyms":"ZFYVE2","biotype":"protein_coding","ncbi_id":"8411","summary":null,"start":92770637,"end":92929331,"strand":-1,"description":"early endosome antigen 1 [Source:HGNC Symbol;Acc:HGNC:3185]"}, {"versioned_ensembl_gene_id":"ENSG00000234219.1","gene_symbol":"CDCA4P4","gene_name":"cell division cycle associated 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49773]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100188945","summary":null,"start":207762584,"end":207763263,"strand":1,"description":"cell division cycle associated 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49773]"}, {"versioned_ensembl_gene_id":"ENSG00000255507.5","gene_symbol":"AP003031.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75803431,"end":75815406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233307.1","gene_symbol":"AC011753.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109732731,"end":109733136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115507.9","gene_symbol":"OTX1","gene_name":"orthodenticle homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8521]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5013","summary":"This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. A similar protein in mouse is required for proper brain and sensory organ development and can cause epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":63050057,"end":63057836,"strand":1,"description":"orthodenticle homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8521]"}, {"versioned_ensembl_gene_id":"ENSG00000279602.1","gene_symbol":"AC109326.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":43360041,"end":43361361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283411.1","gene_symbol":"AL590627.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":137605744,"end":137711018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184361.12","gene_symbol":"SPATA32","gene_name":"spermatogenesis associated 32 [Source:HGNC Symbol;Acc:HGNC:26349]","synonyms":"VAD1.2,TEX34,FLJ25414,C17orf46,AEP2","biotype":"protein_coding","ncbi_id":"124783","summary":null,"start":45254393,"end":45262112,"strand":-1,"description":"spermatogenesis associated 32 [Source:HGNC Symbol;Acc:HGNC:26349]"}, {"versioned_ensembl_gene_id":"ENSG00000275954.5","gene_symbol":"TBC1D3F","gene_name":"TBC1 domain family member 3F [Source:HGNC Symbol;Acc:HGNC:18257]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84218","summary":null,"start":36428618,"end":36439566,"strand":-1,"description":"TBC1 domain family member 3F [Source:HGNC Symbol;Acc:HGNC:18257]"}, {"versioned_ensembl_gene_id":"ENSG00000234319.1","gene_symbol":"RPS12P2","gene_name":"ribosomal protein S12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24221]","synonyms":"bA40F6.3","biotype":"processed_pseudogene","ncbi_id":"619448","summary":null,"start":80215851,"end":80216119,"strand":-1,"description":"ribosomal protein S12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24221]"}, {"versioned_ensembl_gene_id":"ENSG00000231628.1","gene_symbol":"AL133406.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105279016,"end":105281755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248015.6","gene_symbol":"AC005329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1392170,"end":1396467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254980.1","gene_symbol":"AP002008.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111514043,"end":111526755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267680.5","gene_symbol":"ZNF224","gene_name":"zinc finger protein 224 [Source:HGNC Symbol;Acc:HGNC:13017]","synonyms":"ZNF27,ZNF255,KOX22,BMZF-2","biotype":"protein_coding","ncbi_id":"7767","summary":"This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein represses transcription of the aldolase A gene, which encodes a key enzyme in glycolysis. The encoded zinc-finger protein may also function as a transcriptional co-activator with Wilms' tumor protein 1 to regulate apoptotic genes in leukemia. [provided by RefSeq, Jul 2016]","start":44094339,"end":44109886,"strand":1,"description":"zinc finger protein 224 [Source:HGNC Symbol;Acc:HGNC:13017]"}, {"versioned_ensembl_gene_id":"ENSG00000185869.14","gene_symbol":"ZNF829","gene_name":"zinc finger protein 829 [Source:HGNC Symbol;Acc:HGNC:34032]","synonyms":"DKFZp779O175","biotype":"protein_coding","ncbi_id":"374899","summary":null,"start":36888124,"end":36916291,"strand":-1,"description":"zinc finger protein 829 [Source:HGNC Symbol;Acc:HGNC:34032]"}, {"versioned_ensembl_gene_id":"ENSG00000216548.2","gene_symbol":"AL357084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140922457,"end":140922910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166391.14","gene_symbol":"MOGAT2","gene_name":"monoacylglycerol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:23248]","synonyms":"FLJ22644,DGAT2L5,MGAT2","biotype":"protein_coding","ncbi_id":"80168","summary":"The protein encoded by this gene is an enzyme that catalyzes the synthesis of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. The encoded protein is important in the uptake of dietary fat by the small intestine. This protein forms a complex with diacylglycerol O-acyltransferase 2 in the endoplasmic reticulum, and this complex catalyzes the synthesis of triacylglycerol. [provided by RefSeq, Dec 2015]","start":75717819,"end":75732958,"strand":1,"description":"monoacylglycerol O-acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:23248]"}, {"versioned_ensembl_gene_id":"ENSG00000258813.2","gene_symbol":"AL442663.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73057925,"end":73059415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225200.2","gene_symbol":"AC246787.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105978520,"end":105979146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228706.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29789369,"end":29790366,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000213946.3","gene_symbol":"DNAJB1P1","gene_name":"DnaJ heat shock protein family (Hsp40) member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24988]","synonyms":"psiHSP40,DNAJB1P","biotype":"processed_pseudogene","ncbi_id":"171221","summary":null,"start":191881182,"end":191882205,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24988]"}, {"versioned_ensembl_gene_id":"ENSG00000150750.7","gene_symbol":"C11orf53","gene_name":"chromosome 11 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:30527]","synonyms":"MGC50104","biotype":"protein_coding","ncbi_id":"341032","summary":null,"start":111245805,"end":111286401,"strand":1,"description":"chromosome 11 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:30527]"}, {"versioned_ensembl_gene_id":"ENSG00000165115.14","gene_symbol":"KIF27","gene_name":"kinesin family member 27 [Source:HGNC Symbol;Acc:HGNC:18632]","synonyms":"DKFZp434D0917","biotype":"protein_coding","ncbi_id":"55582","summary":"This gene is a member of the KIF27 (kinesin 4) sub-family of the mammalian kinesin family. The gene is an ortholog of the Drosophila Cos2 gene, which plays an important role in the Hedgehog signaling pathway. The encoded protein contains an N-terminal motor domain which includes nucleotide-binding and microtubule-interacting regions, a stalk domain containing a predicted coiled coil motif and a C-terminal tail domain. Alternatively spliced transcript variants have been observed for this gene. Pseudogenes associated with this gene are located on chromosome 9. [provided by RefSeq, Dec 2012]","start":83836698,"end":83921465,"strand":-1,"description":"kinesin family member 27 [Source:HGNC Symbol;Acc:HGNC:18632]"}, {"versioned_ensembl_gene_id":"ENSG00000255035.2","gene_symbol":"SDHCP4","gene_name":"succinate dehydrogenase complex subunit C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422598","summary":null,"start":17435672,"end":17436181,"strand":-1,"description":"succinate dehydrogenase complex subunit C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45179]"}, {"versioned_ensembl_gene_id":"ENSG00000217165.1","gene_symbol":"ANKRD18EP","gene_name":"ankyrin repeat domain 18E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43609]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131031","summary":null,"start":39110321,"end":39112952,"strand":1,"description":"ankyrin repeat domain 18E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43609]"}, {"versioned_ensembl_gene_id":"ENSG00000091664.7","gene_symbol":"SLC17A6","gene_name":"solute carrier family 17 member 6 [Source:HGNC Symbol;Acc:HGNC:16703]","synonyms":"VGLUT2,DNPI","biotype":"protein_coding","ncbi_id":"57084","summary":null,"start":22338097,"end":22379503,"strand":1,"description":"solute carrier family 17 member 6 [Source:HGNC Symbol;Acc:HGNC:16703]"}, {"versioned_ensembl_gene_id":"ENSG00000234918.1","gene_symbol":"AL157387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37240887,"end":37242049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170802.15","gene_symbol":"FOXN2","gene_name":"forkhead box N2 [Source:HGNC Symbol;Acc:HGNC:5281]","synonyms":"HTLF","biotype":"protein_coding","ncbi_id":"3344","summary":"This gene encodes a forkhead domain binding protein and may function in the transcriptional regulation of the human T-cell leukemia virus long terminal repeat. [provided by RefSeq, Jul 2008]","start":48314637,"end":48379294,"strand":1,"description":"forkhead box N2 [Source:HGNC Symbol;Acc:HGNC:5281]"}, {"versioned_ensembl_gene_id":"ENSG00000111358.13","gene_symbol":"GTF2H3","gene_name":"general transcription factor IIH subunit 3 [Source:HGNC Symbol;Acc:HGNC:4657]","synonyms":"BTF2,TFIIH,P34","biotype":"protein_coding","ncbi_id":"2967","summary":"This gene encodes a member of the TFB4 family. The encoded protein is a subunit of the core-TFIIH basal transcription factor and localizes to the nucleus. The encoded protein is involved in RNA transcription by RNA polymerase II and nucleotide excision repair and associates with the Cdk-activating kinase complex. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 14. [provided by RefSeq, Dec 2012]","start":123633739,"end":123662606,"strand":1,"description":"general transcription factor IIH subunit 3 [Source:HGNC Symbol;Acc:HGNC:4657]"}, {"versioned_ensembl_gene_id":"ENSG00000279855.1","gene_symbol":"AC005618.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141427295,"end":141427752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276547.1","gene_symbol":"PCDHGB5","gene_name":"protocadherin gamma subfamily B, 5 [Source:HGNC Symbol;Acc:HGNC:8712]","synonyms":"PCDH-GAMMA-B5","biotype":"protein_coding","ncbi_id":"56101","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141397987,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily B, 5 [Source:HGNC Symbol;Acc:HGNC:8712]"}, {"versioned_ensembl_gene_id":"ENSG00000258578.2","gene_symbol":"AC008015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76013679,"end":76014143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225355.1","gene_symbol":"ARL6IP1P2","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44971]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646348","summary":null,"start":36995023,"end":36995585,"strand":1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44971]"}, {"versioned_ensembl_gene_id":"ENSG00000255882.1","gene_symbol":"AC091814.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9867027,"end":9869808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198624.12","gene_symbol":"CCDC69","gene_name":"coiled-coil domain containing 69 [Source:HGNC Symbol;Acc:HGNC:24487]","synonyms":"FLJ13705,DKFZP434C171","biotype":"protein_coding","ncbi_id":"26112","summary":null,"start":151181052,"end":151224145,"strand":-1,"description":"coiled-coil domain containing 69 [Source:HGNC Symbol;Acc:HGNC:24487]"}, {"versioned_ensembl_gene_id":"ENSG00000134207.15","gene_symbol":"SYT6","gene_name":"synaptotagmin 6 [Source:HGNC Symbol;Acc:HGNC:18638]","synonyms":null,"biotype":"protein_coding","ncbi_id":"148281","summary":"The protein encoded by this gene belongs to the synaptotagmin family. Synaptotagmins share a common domain structure that includes a transmembrane domain and a cytoplasmic region composed of 2 C2 domains, and are involved in calcium-dependent exocytosis of synaptic vesicles. This protein has been shown to be a key component of the secretory machinery involved in acrosomal exocytosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2011]","start":114089291,"end":114153919,"strand":-1,"description":"synaptotagmin 6 [Source:HGNC Symbol;Acc:HGNC:18638]"}, {"versioned_ensembl_gene_id":"ENSG00000272070.1","gene_symbol":"AC005618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141326210,"end":141329357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226646.1","gene_symbol":"RPL7P37","gene_name":"ribosomal protein L7 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36656]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"439954","summary":null,"start":35697300,"end":35698037,"strand":1,"description":"ribosomal protein L7 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36656]"}, {"versioned_ensembl_gene_id":"ENSG00000270509.1","gene_symbol":"AL713998.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67933485,"end":67934682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276487.1","gene_symbol":"AC061709.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128187934,"end":128191389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161714.11","gene_symbol":"PLCD3","gene_name":"phospholipase C delta 3 [Source:HGNC Symbol;Acc:HGNC:9061]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113026","summary":"This gene encodes a member of the phospholipase C family, which catalyze the hydrolysis of phosphatidylinositol 4,5-bisphosphate to generate the second messengers diacylglycerol and inositol 1,4,5-trisphosphate (IP3). Diacylglycerol and IP3 mediate a variety of cellular responses to extracellular stimuli by inducing protein kinase C and increasing cytosolic Ca(2+) concentrations. This enzyme localizes to the plasma membrane and requires calcium for activation. Its activity is inhibited by spermine, sphingosine, and several phospholipids. [provided by RefSeq, Jul 2008]","start":45108967,"end":45133354,"strand":-1,"description":"phospholipase C delta 3 [Source:HGNC Symbol;Acc:HGNC:9061]"}, {"versioned_ensembl_gene_id":"ENSG00000256912.1","gene_symbol":"AC007068.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9817350,"end":9818025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211892.4","gene_symbol":"IGHG4","gene_name":"immunoglobulin heavy constant gamma 4 (G4m marker) [Source:HGNC Symbol;Acc:HGNC:5528]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3503","summary":null,"start":105620506,"end":105626066,"strand":-1,"description":"immunoglobulin heavy constant gamma 4 (G4m marker) [Source:HGNC Symbol;Acc:HGNC:5528]"}, {"versioned_ensembl_gene_id":"ENSG00000160181.8","gene_symbol":"TFF2","gene_name":"trefoil factor 2 [Source:HGNC Symbol;Acc:HGNC:11756]","synonyms":"SML1","biotype":"protein_coding","ncbi_id":"7032","summary":"Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer and affect healing of the epithelium. The encoded protein inhibits gastric acid secretion. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21. [provided by RefSeq, Jul 2008]","start":42346357,"end":42351128,"strand":-1,"description":"trefoil factor 2 [Source:HGNC Symbol;Acc:HGNC:11756]"}, {"versioned_ensembl_gene_id":"ENSG00000156127.6","gene_symbol":"BATF","gene_name":"basic leucine zipper ATF-like transcription factor [Source:HGNC Symbol;Acc:HGNC:958]","synonyms":"SFA-2,BATF1,B-ATF","biotype":"protein_coding","ncbi_id":"10538","summary":"The protein encoded by this gene is a nuclear basic leucine zipper protein that belongs to the AP-1/ATF superfamily of transcription factors. The leucine zipper of this protein mediates dimerization with members of the Jun family of proteins. This protein is thought to be a negative regulator of AP-1/ATF transcriptional events. [provided by RefSeq, Jul 2008]","start":75522425,"end":75547015,"strand":1,"description":"basic leucine zipper ATF-like transcription factor [Source:HGNC Symbol;Acc:HGNC:958]"}, {"versioned_ensembl_gene_id":"ENSG00000231420.1","gene_symbol":"LINC01817","gene_name":"long intergenic non-protein coding RNA 1817 [Source:HGNC Symbol;Acc:HGNC:52622]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373683","summary":null,"start":150234892,"end":150257007,"strand":-1,"description":"long intergenic non-protein coding RNA 1817 [Source:HGNC Symbol;Acc:HGNC:52622]"}, {"versioned_ensembl_gene_id":"ENSG00000230645.1","gene_symbol":"LINC01818","gene_name":"long intergenic non-protein coding RNA 1818 [Source:HGNC Symbol;Acc:HGNC:52623]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373684","summary":null,"start":150171423,"end":150301080,"strand":1,"description":"long intergenic non-protein coding RNA 1818 [Source:HGNC Symbol;Acc:HGNC:52623]"}, {"versioned_ensembl_gene_id":"ENSG00000226825.1","gene_symbol":"LINC01509","gene_name":"long intergenic non-protein coding RNA 1509 [Source:HGNC Symbol;Acc:HGNC:51193]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928720","summary":null,"start":107420284,"end":107430802,"strand":-1,"description":"long intergenic non-protein coding RNA 1509 [Source:HGNC Symbol;Acc:HGNC:51193]"}, {"versioned_ensembl_gene_id":"ENSG00000229698.11","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29720539,"end":29736235,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000226267.1","gene_symbol":"BX005428.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745983,"end":29746207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092439.13","gene_symbol":"TRPM7","gene_name":"transient receptor potential cation channel subfamily M member 7 [Source:HGNC Symbol;Acc:HGNC:17994]","synonyms":"TRP-PLIK,LTRPC7,CHAK1","biotype":"protein_coding","ncbi_id":"54822","summary":"This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017]","start":50552473,"end":50686815,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 7 [Source:HGNC Symbol;Acc:HGNC:17994]"}, {"versioned_ensembl_gene_id":"ENSG00000284730.1","gene_symbol":"AC068987.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":51813940,"end":51814926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259684.1","gene_symbol":"AC084756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50557601,"end":50560500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197172.10","gene_symbol":"MAGEA6","gene_name":"MAGE family member A6 [Source:HGNC Symbol;Acc:HGNC:6804]","synonyms":"MAGE3B,MAGE-3b,CT1.6,MAGE6","biotype":"protein_coding","ncbi_id":"4105","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":152766136,"end":152769747,"strand":-1,"description":"MAGE family member A6 [Source:HGNC Symbol;Acc:HGNC:6804]"}, {"versioned_ensembl_gene_id":"ENSG00000214189.8","gene_symbol":"ZNF788","gene_name":"zinc finger family member 788 [Source:HGNC Symbol;Acc:HGNC:33112]","synonyms":"FLJ46419","biotype":"protein_coding","ncbi_id":"388507","summary":null,"start":12092263,"end":12137235,"strand":1,"description":"zinc finger family member 788 [Source:HGNC Symbol;Acc:HGNC:33112]"}, {"versioned_ensembl_gene_id":"ENSG00000242615.1","gene_symbol":"AC022415.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":12141806,"end":12143322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231652.2","gene_symbol":"AL590428.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73693903,"end":73696131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149257.13","gene_symbol":"SERPINH1","gene_name":"serpin family H member 1 [Source:HGNC Symbol;Acc:HGNC:1546]","synonyms":"SERPINH2,HSP47,colligen,CBP2,CBP1","biotype":"protein_coding","ncbi_id":"871","summary":"This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The encoded protein is localized to the endoplasmic reticulum and plays a role in collagen biosynthesis as a collagen-specific molecular chaperone. Autoantibodies to the encoded protein have been found in patients with rheumatoid arthritis. Expression of this gene may be a marker for cancer, and nucleotide polymorphisms in this gene may be associated with preterm birth caused by preterm premature rupture of membranes. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, May 2011]","start":75562056,"end":75572783,"strand":1,"description":"serpin family H member 1 [Source:HGNC Symbol;Acc:HGNC:1546]"}, {"versioned_ensembl_gene_id":"ENSG00000187918.5","gene_symbol":"OR51I2","gene_name":"olfactory receptor family 51 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15201]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390064","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5449323,"end":5456518,"strand":1,"description":"olfactory receptor family 51 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15201]"}, {"versioned_ensembl_gene_id":"ENSG00000275431.1","gene_symbol":"AC244100.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35983656,"end":35990270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258460.1","gene_symbol":"AL355096.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101332516,"end":101334331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258497.1","gene_symbol":"AL359682.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101257332,"end":101278318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258681.1","gene_symbol":"AL355836.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101217372,"end":101218241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174799.10","gene_symbol":"CEP135","gene_name":"centrosomal protein 135 [Source:HGNC Symbol;Acc:HGNC:29086]","synonyms":"FLJ13621,CEP4,KIAA0635","biotype":"protein_coding","ncbi_id":"9662","summary":"This gene encodes a centrosomal protein, which acts as a scaffolding protein during early centriole biogenesis, and is also required for centriole-centriole cohesion during interphase. Mutations in this gene are associated with autosomal recessive primary microcephaly-8. [provided by RefSeq, Jun 2012]","start":55948871,"end":56033363,"strand":1,"description":"centrosomal protein 135 [Source:HGNC Symbol;Acc:HGNC:29086]"}, {"versioned_ensembl_gene_id":"ENSG00000223735.1","gene_symbol":"OR51B3P","gene_name":"olfactory receptor family 51 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14706]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79342","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5314772,"end":5315684,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14706]"}, {"versioned_ensembl_gene_id":"ENSG00000103355.13","gene_symbol":"PRSS33","gene_name":"protease, serine 33 [Source:HGNC Symbol;Acc:HGNC:30405]","synonyms":"EOS","biotype":"protein_coding","ncbi_id":"260429","summary":null,"start":2783953,"end":2787948,"strand":-1,"description":"protease, serine 33 [Source:HGNC Symbol;Acc:HGNC:30405]"}, {"versioned_ensembl_gene_id":"ENSG00000214546.3","gene_symbol":"AC087491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39619613,"end":39622513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116774.11","gene_symbol":"OLFML3","gene_name":"olfactomedin like 3 [Source:HGNC Symbol;Acc:HGNC:24956]","synonyms":"OLF44,HNOEL-iso","biotype":"protein_coding","ncbi_id":"56944","summary":"This gene encodes a member of the olfactomedin-like gene family which also includes genes encoding noelin, tiarin, myocilin, amassin, optimedin, photomedin, and latrophilin. The encoded protein is a secreted extracellular matrix glycoprotein with a C-terminal olfactomedin domain that facilitates protein-protein interactions, cell adhesion, and intercellular interactions. It serves as both a scaffold protein that recruits bone morphogenetic protein 1 to its substrate chordin, and as a vascular tissue remodeler with pro-angiogenic properties. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":113979391,"end":114035572,"strand":1,"description":"olfactomedin like 3 [Source:HGNC Symbol;Acc:HGNC:24956]"}, {"versioned_ensembl_gene_id":"ENSG00000116957.12","gene_symbol":"TBCE","gene_name":"tubulin folding cofactor E [Source:HGNC Symbol;Acc:HGNC:11582]","synonyms":"pac2,KCS1,KCS,HRD","biotype":"protein_coding","ncbi_id":"6905","summary":"Cofactor E is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":235367360,"end":235448968,"strand":1,"description":"tubulin folding cofactor E [Source:HGNC Symbol;Acc:HGNC:11582]"}, {"versioned_ensembl_gene_id":"ENSG00000156642.16","gene_symbol":"NPTN","gene_name":"neuroplastin [Source:HGNC Symbol;Acc:HGNC:17867]","synonyms":"SDFR1,np65,np55,GP65,GP55,SDR1","biotype":"protein_coding","ncbi_id":"27020","summary":"This gene encodes a type I transmembrane protein belonging to the Ig superfamily. The protein is believed to be involved in cell-cell interactions or cell-substrate interactions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2009]","start":73560014,"end":73634134,"strand":-1,"description":"neuroplastin [Source:HGNC Symbol;Acc:HGNC:17867]"}, {"versioned_ensembl_gene_id":"ENSG00000279068.1","gene_symbol":"AC244517.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":141182409,"end":141188582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272674.3","gene_symbol":"PCDHB16","gene_name":"protocadherin beta 16 [Source:HGNC Symbol;Acc:HGNC:14546]","synonyms":"PCDHB8a,PCDH3X,PCDH-BETA16,ME1,KIAA1621","biotype":"protein_coding","ncbi_id":"57717","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141181399,"end":141186399,"strand":1,"description":"protocadherin beta 16 [Source:HGNC Symbol;Acc:HGNC:14546]"}, {"versioned_ensembl_gene_id":"ENSG00000250257.1","gene_symbol":"LDHAL6DP","gene_name":"lactate dehydrogenase A like 6D, pseudogene [Source:HGNC Symbol;Acc:HGNC:44239]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420508","summary":null,"start":83814571,"end":83815263,"strand":-1,"description":"lactate dehydrogenase A like 6D, pseudogene [Source:HGNC Symbol;Acc:HGNC:44239]"}, {"versioned_ensembl_gene_id":"ENSG00000240777.2","gene_symbol":"AC025572.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55610603,"end":55613104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253304.1","gene_symbol":"TMEM200B","gene_name":"transmembrane protein 200B [Source:HGNC Symbol;Acc:HGNC:33785]","synonyms":"TTMB","biotype":"protein_coding","ncbi_id":"399474","summary":null,"start":29119428,"end":29123935,"strand":-1,"description":"transmembrane protein 200B [Source:HGNC Symbol;Acc:HGNC:33785]"}, {"versioned_ensembl_gene_id":"ENSG00000187672.12","gene_symbol":"ERC2","gene_name":"ELKS/RAB6-interacting/CAST family member 2 [Source:HGNC Symbol;Acc:HGNC:31922]","synonyms":"Spc110,SPBC110,KIAA0378,ELKSL,CAST1,CAST","biotype":"protein_coding","ncbi_id":"26059","summary":"This gene encodes a protein that belongs to the Rab3-interacting molecule (RIM)-binding protein family. Members of this protein family form part of the cytomatrix at the active zone (CAZ) complex and function as regulators of neurotransmitter release. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":55508308,"end":56468363,"strand":-1,"description":"ELKS/RAB6-interacting/CAST family member 2 [Source:HGNC Symbol;Acc:HGNC:31922]"}, {"versioned_ensembl_gene_id":"ENSG00000257402.2","gene_symbol":"KRT126P","gene_name":"keratin 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:32970]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643865","summary":null,"start":52715567,"end":52721655,"strand":-1,"description":"keratin 126 pseudogene [Source:HGNC Symbol;Acc:HGNC:32970]"}, {"versioned_ensembl_gene_id":"ENSG00000197479.6","gene_symbol":"PCDHB11","gene_name":"protocadherin beta 11 [Source:HGNC Symbol;Acc:HGNC:8682]","synonyms":"ME2,PCDH-BETA11","biotype":"protein_coding","ncbi_id":"56125","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141199582,"end":141203779,"strand":1,"description":"protocadherin beta 11 [Source:HGNC Symbol;Acc:HGNC:8682]"}, {"versioned_ensembl_gene_id":"ENSG00000240174.1","gene_symbol":"AP000852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84639993,"end":84640565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234669.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672889,"end":29681605,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000253404.1","gene_symbol":"AC034243.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138744434,"end":138753309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235612.1","gene_symbol":"AL353681.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56145721,"end":56155224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178631.7","gene_symbol":"ACTG1P1","gene_name":"actin gamma 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:146]","synonyms":"ACTGP1,ACT1GP1","biotype":"processed_pseudogene","ncbi_id":"73","summary":null,"start":139493809,"end":139494937,"strand":1,"description":"actin gamma 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:146]"}, {"versioned_ensembl_gene_id":"ENSG00000276462.1","gene_symbol":"BX255923.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41100794,"end":41106229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281207.1","gene_symbol":"SLFNL1-AS1","gene_name":"SLFNL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44126]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507178","summary":null,"start":41014590,"end":41043890,"strand":1,"description":"SLFNL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44126]"}, {"versioned_ensembl_gene_id":"ENSG00000276842.1","gene_symbol":"AC023510.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25103124,"end":25103869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139651.10","gene_symbol":"ZNF740","gene_name":"zinc finger protein 740 [Source:HGNC Symbol;Acc:HGNC:27465]","synonyms":"Zfp740","biotype":"protein_coding","ncbi_id":"283337","summary":null,"start":53180700,"end":53195141,"strand":1,"description":"zinc finger protein 740 [Source:HGNC Symbol;Acc:HGNC:27465]"}, {"versioned_ensembl_gene_id":"ENSG00000233569.1","gene_symbol":"AL161630.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117648606,"end":117657027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235133.1","gene_symbol":"RPL35AP22","gene_name":"ribosomal protein L35a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271507","summary":null,"start":117685254,"end":117685588,"strand":-1,"description":"ribosomal protein L35a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35932]"}, {"versioned_ensembl_gene_id":"ENSG00000233516.1","gene_symbol":"AL445644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117462294,"end":117466260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234514.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31662426,"end":31665209,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000225420.1","gene_symbol":"AC104134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88538720,"end":88575610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273372.1","gene_symbol":"SFTPD-AS1","gene_name":"SFTPD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51589]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105419997","summary":null,"start":79968213,"end":79973213,"strand":1,"description":"SFTPD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51589]"}, {"versioned_ensembl_gene_id":"ENSG00000224817.1","gene_symbol":"AC010789.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101704652,"end":101708401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176752.6","gene_symbol":"OR51A1P","gene_name":"olfactory receptor family 51 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8316]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"26537","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5170351,"end":5171296,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8316]"}, {"versioned_ensembl_gene_id":"ENSG00000282581.1","gene_symbol":"AC138747.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28427760,"end":28427964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189393.5","gene_symbol":"FAM90A14P","gene_name":"family with sequence similarity 90 member A14, pseudogene [Source:HGNC Symbol;Acc:HGNC:32262]","synonyms":"FAM90A14","biotype":"unprocessed_pseudogene","ncbi_id":"645651","summary":"FAM90A14 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, May 2010]","start":7715443,"end":7718453,"strand":1,"description":"family with sequence similarity 90 member A14, pseudogene [Source:HGNC Symbol;Acc:HGNC:32262]"}, {"versioned_ensembl_gene_id":"ENSG00000250267.2","gene_symbol":"AC021237.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109298598,"end":109316513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213264.3","gene_symbol":"NIP7P2","gene_name":"NIP7, nucleolar pre-rRNA processing protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45181]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646392","summary":null,"start":132401253,"end":132401796,"strand":1,"description":"NIP7, nucleolar pre-rRNA processing protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45181]"}, {"versioned_ensembl_gene_id":"ENSG00000233309.1","gene_symbol":"RPS6P12","gene_name":"ribosomal protein S6 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270867","summary":null,"start":82744067,"end":82744792,"strand":-1,"description":"ribosomal protein S6 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36375]"}, {"versioned_ensembl_gene_id":"ENSG00000102794.9","gene_symbol":"ACOD1","gene_name":"aconitate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:33904]","synonyms":"IRG1,CAD","biotype":"protein_coding","ncbi_id":"730249","summary":null,"start":76948497,"end":76958642,"strand":1,"description":"aconitate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:33904]"}, {"versioned_ensembl_gene_id":"ENSG00000275311.1","gene_symbol":"AC139494.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69758658,"end":69759641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099812.8","gene_symbol":"MISP","gene_name":"mitotic spindle positioning [Source:HGNC Symbol;Acc:HGNC:27000]","synonyms":"MISP1,DKFZp686H18209,Caprice,C19orf21","biotype":"protein_coding","ncbi_id":"126353","summary":"The protein encoded by this gene is an actin-bundling protein involved in determining cell morphology and mitotic progression. The encoded protein is required for the proper positioning of the mitotic spindle. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Feb 2016]","start":751126,"end":764318,"strand":1,"description":"mitotic spindle positioning [Source:HGNC Symbol;Acc:HGNC:27000]"}, {"versioned_ensembl_gene_id":"ENSG00000248510.2","gene_symbol":"LINC02267","gene_name":"long intergenic non-protein coding RNA 2267 [Source:HGNC Symbol;Acc:HGNC:53181]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377338","summary":null,"start":96310701,"end":96818864,"strand":1,"description":"long intergenic non-protein coding RNA 2267 [Source:HGNC Symbol;Acc:HGNC:53181]"}, {"versioned_ensembl_gene_id":"ENSG00000170667.14","gene_symbol":"RASA4B","gene_name":"RAS p21 protein activator 4B [Source:HGNC Symbol;Acc:HGNC:35202]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100271927","summary":null,"start":102482445,"end":102517781,"strand":-1,"description":"RAS p21 protein activator 4B [Source:HGNC Symbol;Acc:HGNC:35202]"}, {"versioned_ensembl_gene_id":"ENSG00000274722.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54836820,"end":54853592,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000277036.1","gene_symbol":"AC139494.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69761566,"end":69762272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174417.2","gene_symbol":"TRHR","gene_name":"thyrotropin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:12299]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7201","summary":"This gene encodes a G protein-coupled receptor for thyrotropin-releasing hormone (TRH). Upon binding to TRH, this receptor activates the inositol phospholipid-calcium-protein kinase C transduction pathway. Mutations in this gene have been associated with generalized thyrotropin-releasing hormone resistance. [provided by RefSeq, Sep 2011]","start":109086621,"end":109119584,"strand":1,"description":"thyrotropin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:12299]"}, {"versioned_ensembl_gene_id":"ENSG00000278727.1","gene_symbol":"AC000403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76887551,"end":76891135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142937.11","gene_symbol":"RPS8","gene_name":"ribosomal protein S8 [Source:HGNC Symbol;Acc:HGNC:10441]","synonyms":"S8","biotype":"protein_coding","ncbi_id":"6202","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S8E family of ribosomal proteins. It is located in the cytoplasm. Increased expression of this gene in colorectal tumors and colon polyps compared to matched normal colonic mucosa has been observed. This gene is co-transcribed with the small nucleolar RNA genes U38A, U38B, U39, and U40, which are located in its fourth, fifth, first, and second introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":44775251,"end":44778779,"strand":1,"description":"ribosomal protein S8 [Source:HGNC Symbol;Acc:HGNC:10441]"}, {"versioned_ensembl_gene_id":"ENSG00000267595.1","gene_symbol":"AC060780.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43168170,"end":43168249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255315.1","gene_symbol":"AP000916.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":124531625,"end":124531910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277606.4","gene_symbol":"AC118459.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69856054,"end":69898246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254646.1","gene_symbol":"OR8B10P","gene_name":"olfactory receptor family 8 subfamily B member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:14751]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390274","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124516311,"end":124517242,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:14751]"}, {"versioned_ensembl_gene_id":"ENSG00000022267.16","gene_symbol":"FHL1","gene_name":"four and a half LIM domains 1 [Source:HGNC Symbol;Acc:HGNC:3702]","synonyms":"SLIM1,MGC111107,KYO-T,FLH1A,FHL1B,bA535K18.1,XMPMA","biotype":"protein_coding","ncbi_id":"2273","summary":"This gene encodes a member of the four-and-a-half-LIM-only protein family. Family members contain two highly conserved, tandemly arranged, zinc finger domains with four highly conserved cysteines binding a zinc atom in each zinc finger. Expression of these family members occurs in a cell- and tissue-specific mode and these proteins are involved in many cellular processes. Mutations in this gene have been found in patients with Emery-Dreifuss muscular dystrophy. Multiple alternately spliced transcript variants which encode different protein isoforms have been described.[provided by RefSeq, Nov 2009]","start":136146702,"end":136211359,"strand":1,"description":"four and a half LIM domains 1 [Source:HGNC Symbol;Acc:HGNC:3702]"}, {"versioned_ensembl_gene_id":"ENSG00000284617.1","gene_symbol":"AC134684.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7611473,"end":7611690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258405.9","gene_symbol":"ZNF578","gene_name":"zinc finger protein 578 [Source:HGNC Symbol;Acc:HGNC:26449]","synonyms":"FLJ31384","biotype":"protein_coding","ncbi_id":"147660","summary":null,"start":52453576,"end":52512154,"strand":1,"description":"zinc finger protein 578 [Source:HGNC Symbol;Acc:HGNC:26449]"}, {"versioned_ensembl_gene_id":"ENSG00000278543.1","gene_symbol":"AC010332.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52473336,"end":52475239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166762.16","gene_symbol":"CATSPER2","gene_name":"cation channel sperm associated 2 [Source:HGNC Symbol;Acc:HGNC:18810]","synonyms":null,"biotype":"protein_coding","ncbi_id":"117155","summary":"This gene encodes a member of a family of cation channel proteins that localize to the flagellum of spermatozoa. Defects at this locus causes male infertility. Alternatively spliced transcript variants have been observed at this locus. Readthrough transcription originates upstream of this locus in diphosphoinositol pentakisphosphate kinase 1 pseudogene 1 and is represented by GeneID:110006325. Related pseudogenes are found next to this locus on chromosome 15 and on chromosome 5. [provided by RefSeq, Mar 2017]","start":43628503,"end":43668118,"strand":-1,"description":"cation channel sperm associated 2 [Source:HGNC Symbol;Acc:HGNC:18810]"}, {"versioned_ensembl_gene_id":"ENSG00000230261.1","gene_symbol":"OR52J2P","gene_name":"olfactory receptor family 52 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14797]","synonyms":"OR52J4P","biotype":"unprocessed_pseudogene","ncbi_id":"79529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5037013,"end":5037951,"strand":1,"description":"olfactory receptor family 52 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14797]"}, {"versioned_ensembl_gene_id":"ENSG00000214980.4","gene_symbol":"AC025538.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84244003,"end":84245488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272853.1","gene_symbol":"AC069544.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14877688,"end":14878686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109390.11","gene_symbol":"NDUFC1","gene_name":"NADH:ubiquinone oxidoreductase subunit C1 [Source:HGNC Symbol;Acc:HGNC:7705]","synonyms":"KFYI","biotype":"protein_coding","ncbi_id":"4717","summary":"The encoded protein is a subunit of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":139266880,"end":139302551,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit C1 [Source:HGNC Symbol;Acc:HGNC:7705]"}, {"versioned_ensembl_gene_id":"ENSG00000223952.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31651872,"end":31654641,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000185863.7","gene_symbol":"TMEM210","gene_name":"transmembrane protein 210 [Source:HGNC Symbol;Acc:HGNC:34059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505993","summary":null,"start":137170858,"end":137172409,"strand":-1,"description":"transmembrane protein 210 [Source:HGNC Symbol;Acc:HGNC:34059]"}, {"versioned_ensembl_gene_id":"ENSG00000272519.1","gene_symbol":"AC079610.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":213266995,"end":213276152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164587.11","gene_symbol":"RPS14","gene_name":"ribosomal protein S14 [Source:HGNC Symbol;Acc:HGNC:10387]","synonyms":"S14,EMTB","biotype":"protein_coding","ncbi_id":"6208","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S11P family of ribosomal proteins. It is located in the cytoplasm. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. In Chinese hamster ovary cells, mutations in this gene can lead to resistance to emetine, a protein synthesis inhibitor. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":150443190,"end":150449756,"strand":-1,"description":"ribosomal protein S14 [Source:HGNC Symbol;Acc:HGNC:10387]"}, {"versioned_ensembl_gene_id":"ENSG00000270659.1","gene_symbol":"AC079610.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":213152970,"end":213153659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228110.4","gene_symbol":"ST13P19","gene_name":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131961","summary":null,"start":210265636,"end":210267241,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38862]"}, {"versioned_ensembl_gene_id":"ENSG00000279960.1","gene_symbol":"AL137783.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132891924,"end":132893819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264007.1","gene_symbol":"AC104564.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29621617,"end":29622254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241241.1","gene_symbol":"KRTAP4-16","gene_name":"keratin associated protein 4-16 [Source:HGNC Symbol;Acc:HGNC:18921]","synonyms":"KAP4A,KRTAP4P1,KRTAP4-16P","biotype":"protein_coding","ncbi_id":"85354","summary":null,"start":41101502,"end":41102209,"strand":-1,"description":"keratin associated protein 4-16 [Source:HGNC Symbol;Acc:HGNC:18921]"}, {"versioned_ensembl_gene_id":"ENSG00000204880.7","gene_symbol":"KRTAP4-8","gene_name":"keratin associated protein 4-8 [Source:HGNC Symbol;Acc:HGNC:17230]","synonyms":"KAP4.8,KRTAP4.8,KAP4.8","biotype":"protein_coding","ncbi_id":"728224","summary":null,"start":41096981,"end":41098141,"strand":-1,"description":"keratin associated protein 4-8 [Source:HGNC Symbol;Acc:HGNC:17230]"}, {"versioned_ensembl_gene_id":"ENSG00000168237.17","gene_symbol":"GLYCTK","gene_name":"glycerate kinase [Source:HGNC Symbol;Acc:HGNC:24247]","synonyms":"HBEBP4,HBEBP2","biotype":"protein_coding","ncbi_id":"132158","summary":"This locus encodes a member of the glycerate kinase type-2 family. The encoded enzyme catalyzes the phosphorylation of (R)-glycerate and may be involved in serine degradation and fructose metabolism. Decreased activity of the encoded enzyme may be associated with the disease D-glyceric aciduria. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009]","start":52287089,"end":52293476,"strand":1,"description":"glycerate kinase [Source:HGNC Symbol;Acc:HGNC:24247]"}, {"versioned_ensembl_gene_id":"ENSG00000267149.2","gene_symbol":"AC011476.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55027593,"end":55053928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255251.1","gene_symbol":"PRR23D1","gene_name":"proline rich 23 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:49420]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131608","summary":null,"start":7539628,"end":7542450,"strand":1,"description":"proline rich 23 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:49420]"}, {"versioned_ensembl_gene_id":"ENSG00000265469.1","gene_symbol":"AC097641.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73163035,"end":73163359,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140368.12","gene_symbol":"PSTPIP1","gene_name":"proline-serine-threonine phosphatase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9580]","synonyms":"PAPAS,H-PIP,CD2BP1S,CD2BP1L,CD2BP1,PSTPIP","biotype":"protein_coding","ncbi_id":"9051","summary":"This gene encodes a cytoskeletal protein that is highly expressed in hemopoietic tissues. This protein functions via its interaction with several different proteins involved in cytoskeletal organization and inflammatory processes. It binds to the cytoplasmic tail of CD2, an effector of T cell activation and adhesion, downregulating CD2-triggered adhesion. It binds PEST-type protein tyrosine phosphatases (PTP) and directs them to c-Abl kinase to mediate c-Abl dephosphorylation, thereby, regulating c-Abl activity. It also interacts with pyrin, which is found in association with the cytoskeleton in myeloid/monocytic cells and modulates immunoregulatory functions. Mutations in this gene are associated with PAPA (pyogenic sterile arthritis, pyoderma gangrenosum, and acne) syndrome. It is hypothesized that the disease-causing mutations compromise physiologic signaling necessary for the maintenance of a proper inflammatory response. [provided by RefSeq, Mar 2016]","start":76993359,"end":77037332,"strand":1,"description":"proline-serine-threonine phosphatase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9580]"}, {"versioned_ensembl_gene_id":"ENSG00000278901.1","gene_symbol":"AC005609.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140878073,"end":140882642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254092.1","gene_symbol":"AC015468.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20952645,"end":20973877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281943.1","gene_symbol":"TRBV7-9","gene_name":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]","synonyms":"TCRBV6S4A1,TRBV79,TCRBV7S9","biotype":"TR_V_gene","ncbi_id":"28589","summary":null,"start":142571143,"end":142571615,"strand":1,"description":"T-cell receptor beta variable 7-9 [Source:HGNC Symbol;Acc:HGNC:12243]"}, {"versioned_ensembl_gene_id":"ENSG00000283380.1","gene_symbol":"AL807742.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":20769718,"end":21374265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248112.1","gene_symbol":"AC108174.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82919376,"end":82921119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266236.1","gene_symbol":"NARF-IT1","gene_name":"NARF intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43651]","synonyms":"NARF-OT1","biotype":"sense_intronic","ncbi_id":"100506001","summary":null,"start":82482098,"end":82483388,"strand":1,"description":"NARF intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43651]"}, {"versioned_ensembl_gene_id":"ENSG00000020256.19","gene_symbol":"ZFP64","gene_name":"ZFP64 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:15940]","synonyms":"ZNF338,FLJ12628,FLJ10734,dJ831D17.1,dJ548G19.1","biotype":"protein_coding","ncbi_id":"55734","summary":null,"start":52051663,"end":52204308,"strand":-1,"description":"ZFP64 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:15940]"}, {"versioned_ensembl_gene_id":"ENSG00000270187.1","gene_symbol":"IGKV1OR2-11","gene_name":"immunoglobulin kappa variable 1/OR2-11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5768]","synonyms":"IGKV1/OR2-11","biotype":"IG_V_pseudogene","ncbi_id":"28863","summary":null,"start":97386082,"end":97386368,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5768]"}, {"versioned_ensembl_gene_id":"ENSG00000257411.1","gene_symbol":"AC034102.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56101331,"end":56109289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143469.18","gene_symbol":"SYT14","gene_name":"synaptotagmin 14 [Source:HGNC Symbol;Acc:HGNC:23143]","synonyms":"sytXIV,FLJ34198","biotype":"protein_coding","ncbi_id":"255928","summary":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1;3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]","start":209938174,"end":210171389,"strand":1,"description":"synaptotagmin 14 [Source:HGNC Symbol;Acc:HGNC:23143]"}, {"versioned_ensembl_gene_id":"ENSG00000205628.2","gene_symbol":"LINC01446","gene_name":"long intergenic non-protein coding RNA 1446 [Source:HGNC Symbol;Acc:HGNC:50773]","synonyms":"FLJ45974","biotype":"lincRNA","ncbi_id":"401337","summary":null,"start":53655509,"end":53811931,"strand":-1,"description":"long intergenic non-protein coding RNA 1446 [Source:HGNC Symbol;Acc:HGNC:50773]"}, {"versioned_ensembl_gene_id":"ENSG00000224632.1","gene_symbol":"Z73361.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103007461,"end":103008072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272656.1","gene_symbol":"AC024933.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139349024,"end":139349371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225185.3","gene_symbol":"AC013283.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98590723,"end":98591214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259309.1","gene_symbol":"AC021818.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69820756,"end":69822856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217874.2","gene_symbol":"OR4F7P","gene_name":"olfactory receptor family 4 subfamily F member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15089]","synonyms":"OR4F10","biotype":"unprocessed_pseudogene","ncbi_id":"81390","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":170639606,"end":170640536,"strand":1,"description":"olfactory receptor family 4 subfamily F member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15089]"}, {"versioned_ensembl_gene_id":"ENSG00000282470.1","gene_symbol":"TRBV6-7","gene_name":"T-cell receptor beta variable 6-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12232]","synonyms":"TCRBV6S7,TCRBV13S8P,TRBV67","biotype":"TR_V_gene","ncbi_id":"28600","summary":null,"start":142509537,"end":142510011,"strand":1,"description":"T-cell receptor beta variable 6-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12232]"}, {"versioned_ensembl_gene_id":"ENSG00000126218.11","gene_symbol":"F10","gene_name":"coagulation factor X [Source:HGNC Symbol;Acc:HGNC:3528]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2159","summary":"This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015]","start":113122814,"end":113149529,"strand":1,"description":"coagulation factor X [Source:HGNC Symbol;Acc:HGNC:3528]"}, {"versioned_ensembl_gene_id":"ENSG00000255181.3","gene_symbol":"CCDC166","gene_name":"coiled-coil domain containing 166 [Source:HGNC Symbol;Acc:HGNC:41910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130274","summary":null,"start":143706694,"end":143708109,"strand":-1,"description":"coiled-coil domain containing 166 [Source:HGNC Symbol;Acc:HGNC:41910]"}, {"versioned_ensembl_gene_id":"ENSG00000280187.1","gene_symbol":"AC022107.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69186359,"end":69189452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178927.17","gene_symbol":"C17orf62","gene_name":"chromosome 17 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28672]","synonyms":"MGC4368,FLJ90469","biotype":"protein_coding","ncbi_id":"79415","summary":null,"start":82442589,"end":82450829,"strand":-1,"description":"chromosome 17 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:28672]"}, {"versioned_ensembl_gene_id":"ENSG00000181097.5","gene_symbol":"AC105219.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143696154,"end":143698413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232239.2","gene_symbol":"RBPJP5","gene_name":"RBPJ pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37485]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288841","summary":null,"start":39739747,"end":39741193,"strand":-1,"description":"RBPJ pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37485]"}, {"versioned_ensembl_gene_id":"ENSG00000272917.1","gene_symbol":"AC010186.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9642872,"end":9657070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253299.1","gene_symbol":"AC025647.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100165226,"end":100165478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281721.1","gene_symbol":"AL158064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80011077,"end":80028283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165029.15","gene_symbol":"ABCA1","gene_name":"ATP binding cassette subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:29]","synonyms":"TGD,HDLDT1,ABC1","biotype":"protein_coding","ncbi_id":"19","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in both alleles of this gene cause Tangier disease and familial high-density lipoprotein (HDL) deficiency. [provided by RefSeq, Sep 2019]","start":104781002,"end":104928237,"strand":-1,"description":"ATP binding cassette subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:29]"}, {"versioned_ensembl_gene_id":"ENSG00000260634.1","gene_symbol":"AC012508.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127024252,"end":127025723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135750.14","gene_symbol":"KCNK1","gene_name":"potassium two pore domain channel subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:6272]","synonyms":"TWIK-1,K2p1.1,DPK","biotype":"protein_coding","ncbi_id":"3775","summary":"This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008]","start":233614004,"end":233672512,"strand":1,"description":"potassium two pore domain channel subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:6272]"}, {"versioned_ensembl_gene_id":"ENSG00000226367.5","gene_symbol":"ST7-AS2","gene_name":"ST7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16044]","synonyms":"ST7OT2,ST7AS2","biotype":"antisense_RNA","ncbi_id":"93654","summary":null,"start":117072072,"end":117146480,"strand":-1,"description":"ST7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16044]"}, {"versioned_ensembl_gene_id":"ENSG00000111596.11","gene_symbol":"CNOT2","gene_name":"CCR4-NOT transcription complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:7878]","synonyms":"NOT2H,NOT2,CDC36","biotype":"protein_coding","ncbi_id":"4848","summary":"This gene encodes a subunit of the multi-component CCR4-NOT complex. The CCR4-NOT complex regulates mRNA synthesis and degradation and is also thought to be involved in mRNA splicing, transport and localization. The encoded protein interacts with histone deacetylases and functions as a repressor of polymerase II transcription. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]","start":70242994,"end":70354993,"strand":1,"description":"CCR4-NOT transcription complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:7878]"}, {"versioned_ensembl_gene_id":"ENSG00000274021.1","gene_symbol":"AC024909.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89351015,"end":89353271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101773.18","gene_symbol":"RBBP8","gene_name":"RB binding protein 8, endonuclease [Source:HGNC Symbol;Acc:HGNC:9891]","synonyms":"SCKL2,RIM,CtIP,COM1","biotype":"protein_coding","ncbi_id":"5932","summary":"The protein encoded by this gene is a ubiquitously expressed nuclear protein. It is found among several proteins that bind directly to retinoblastoma protein, which regulates cell proliferation. This protein complexes with transcriptional co-repressor CTBP. It is also associated with BRCA1 and is thought to modulate the functions of BRCA1 in transcriptional regulation, DNA repair, and/or cell cycle checkpoint control. It is suggested that this gene may itself be a tumor suppressor acting in the same pathway as BRCA1. Three transcript variants encoding two different isoforms have been found for this gene. More transcript variants exist, but their full-length natures have not been determined. [provided by RefSeq, Jul 2008]","start":22798261,"end":23026488,"strand":1,"description":"RB binding protein 8, endonuclease [Source:HGNC Symbol;Acc:HGNC:9891]"}, {"versioned_ensembl_gene_id":"ENSG00000066084.12","gene_symbol":"DIP2B","gene_name":"disco interacting protein 2 homolog B [Source:HGNC Symbol;Acc:HGNC:29284]","synonyms":"KIAA1463,FLJ34278","biotype":"protein_coding","ncbi_id":"57609","summary":"This gene encodes a member of the disco-interacting protein homolog 2 protein family. The encoded protein contains a binding site for the transcriptional regulator DNA methyltransferase 1 associated protein 1 as well as AMP-binding sites. The presence of these sites suggests that the encoded protein may participate in DNA methylation. This gene is located near a folate-sensitive fragile site, and CGG-repeat expansion in the promoter of this gene which affects transcription has been detected in individuals containing this fragile site on chromosome 12. [provided by RefSeq, Aug 2011]","start":50504985,"end":50748667,"strand":1,"description":"disco interacting protein 2 homolog B [Source:HGNC Symbol;Acc:HGNC:29284]"}, {"versioned_ensembl_gene_id":"ENSG00000259457.1","gene_symbol":"AC100826.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69564724,"end":69565790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159674.11","gene_symbol":"SPON2","gene_name":"spondin 2 [Source:HGNC Symbol;Acc:HGNC:11253]","synonyms":"DIL1","biotype":"protein_coding","ncbi_id":"10417","summary":null,"start":1166932,"end":1208962,"strand":-1,"description":"spondin 2 [Source:HGNC Symbol;Acc:HGNC:11253]"}, {"versioned_ensembl_gene_id":"ENSG00000160888.6","gene_symbol":"IER2","gene_name":"immediate early response 2 [Source:HGNC Symbol;Acc:HGNC:28871]","synonyms":"ETR101","biotype":"protein_coding","ncbi_id":"9592","summary":null,"start":13150415,"end":13154908,"strand":1,"description":"immediate early response 2 [Source:HGNC Symbol;Acc:HGNC:28871]"}, {"versioned_ensembl_gene_id":"ENSG00000135976.17","gene_symbol":"ANKRD36","gene_name":"ankyrin repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:24079]","synonyms":"UNQ2430","biotype":"protein_coding","ncbi_id":"375248","summary":null,"start":97113496,"end":97264521,"strand":1,"description":"ankyrin repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:24079]"}, {"versioned_ensembl_gene_id":"ENSG00000258368.2","gene_symbol":"ZNF970P","gene_name":"zinc finger protein 970, pseudogene [Source:HGNC Symbol;Acc:HGNC:44511]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105369729","summary":null,"start":37575587,"end":37576384,"strand":1,"description":"zinc finger protein 970, pseudogene [Source:HGNC Symbol;Acc:HGNC:44511]"}, {"versioned_ensembl_gene_id":"ENSG00000156509.13","gene_symbol":"FBXO43","gene_name":"F-box protein 43 [Source:HGNC Symbol;Acc:HGNC:28521]","synonyms":"Fbx43","biotype":"protein_coding","ncbi_id":"286151","summary":"Members of the F-box protein family, such as FBXO43, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":100133360,"end":100145800,"strand":-1,"description":"F-box protein 43 [Source:HGNC Symbol;Acc:HGNC:28521]"}, {"versioned_ensembl_gene_id":"ENSG00000267152.1","gene_symbol":"AC093227.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37728586,"end":37730643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231265.1","gene_symbol":"TRERNA1","gene_name":"translation regulatory long non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:44307]","synonyms":"treRNA,ncRNA-a7,LINC00651","biotype":"lincRNA","ncbi_id":"100887755","summary":null,"start":50040716,"end":50041504,"strand":-1,"description":"translation regulatory long non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:44307]"}, {"versioned_ensembl_gene_id":"ENSG00000257820.1","gene_symbol":"AC024909.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89319364,"end":89319649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180044.5","gene_symbol":"C3orf80","gene_name":"chromosome 3 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:40048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401097","summary":null,"start":160225496,"end":160228213,"strand":1,"description":"chromosome 3 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:40048]"}, {"versioned_ensembl_gene_id":"ENSG00000254480.1","gene_symbol":"AC015689.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4187140,"end":4202655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227649.1","gene_symbol":"MTND6P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52173]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075200","summary":null,"start":102806164,"end":102806646,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52173]"}, {"versioned_ensembl_gene_id":"ENSG00000236643.1","gene_symbol":"AL354928.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124770123,"end":124772927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198908.11","gene_symbol":"BHLHB9","gene_name":"basic helix-loop-helix family member b9 [Source:HGNC Symbol;Acc:HGNC:29353]","synonyms":"p60TRP,KIAA1701,GASP3","biotype":"protein_coding","ncbi_id":"80823","summary":"This gene is a member of a gene family which encodes proteins with a basic helix-loop-helix domain. Other members of this gene family encode proteins which function as transcription factors, either enhancing or inhibiting transcription depending on the activity of other DNA binding proteins. The coding region of this gene is located entirely within the terminal exon. The encoded protein may be involved in the survival of neurons (PMID: 15034937). Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]","start":102720688,"end":102753540,"strand":1,"description":"basic helix-loop-helix family member b9 [Source:HGNC Symbol;Acc:HGNC:29353]"}, {"versioned_ensembl_gene_id":"ENSG00000279438.1","gene_symbol":"AP001002.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91093875,"end":91094260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248278.1","gene_symbol":"SUMO2P17","gene_name":"SUMO2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49358]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100128010","summary":null,"start":48874860,"end":48908983,"strand":-1,"description":"SUMO2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49358]"}, {"versioned_ensembl_gene_id":"ENSG00000245482.2","gene_symbol":"AC046130.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34022281,"end":34046417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264491.1","gene_symbol":"AC005544.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67019934,"end":67021743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213486.3","gene_symbol":"AC108039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61710076,"end":61710978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254788.7","gene_symbol":"CKLF-CMTM1","gene_name":"CKLF-CMTM1 readthrough [Source:HGNC Symbol;Acc:HGNC:39977]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529251","summary":"This locus represents naturally occurring read-through transcription between the neighboring CKLF (chemokine-like factor) and CMTM1 (CKLF-like MARVEL transmembrane domain containing 1) genes on chromosome 16. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]","start":66552587,"end":66579135,"strand":1,"description":"CKLF-CMTM1 readthrough [Source:HGNC Symbol;Acc:HGNC:39977]"}, {"versioned_ensembl_gene_id":"ENSG00000136783.9","gene_symbol":"NIPSNAP3A","gene_name":"nipsnap homolog 3A [Source:HGNC Symbol;Acc:HGNC:23619]","synonyms":"MGC14553,HSPC299,FLJ13953,DKFZp564D177","biotype":"protein_coding","ncbi_id":"25934","summary":"NIPSNAP3A belongs to a family of proteins with putative roles in vesicular transport (Buechler et al., 2004 [PubMed 15177564]).[supplied by OMIM, Mar 2008]","start":104747688,"end":104760122,"strand":1,"description":"nipsnap homolog 3A [Source:HGNC Symbol;Acc:HGNC:23619]"}, {"versioned_ensembl_gene_id":"ENSG00000254350.1","gene_symbol":"AC091979.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158424585,"end":158452758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220483.4","gene_symbol":"SLC25A51P1","gene_name":"solute carrier family 25 member 51 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23325]","synonyms":"bA707M13.1,MCART3P","biotype":"processed_pseudogene","ncbi_id":"442229","summary":null,"start":65788417,"end":65789287,"strand":1,"description":"solute carrier family 25 member 51 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23325]"}, {"versioned_ensembl_gene_id":"ENSG00000146013.10","gene_symbol":"GFRA3","gene_name":"GDNF family receptor alpha 3 [Source:HGNC Symbol;Acc:HGNC:4245]","synonyms":"GFRa-3","biotype":"protein_coding","ncbi_id":"2676","summary":"The protein encoded by this gene is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor and a member of the GDNF receptor family. It forms a signaling receptor complex with RET tyrosine kinase receptor and binds the ligand, artemin. [provided by RefSeq, Jul 2008]","start":138252379,"end":138274671,"strand":-1,"description":"GDNF family receptor alpha 3 [Source:HGNC Symbol;Acc:HGNC:4245]"}, {"versioned_ensembl_gene_id":"ENSG00000273423.1","gene_symbol":"OR13I1P","gene_name":"olfactory receptor family 13 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14732]","synonyms":"OR13I2P","biotype":"unprocessed_pseudogene","ncbi_id":"79538","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104629754,"end":104631017,"strand":1,"description":"olfactory receptor family 13 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14732]"}, {"versioned_ensembl_gene_id":"ENSG00000265883.1","gene_symbol":"AC060771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65185319,"end":65185482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276457.1","gene_symbol":"FKBP4P8","gene_name":"FK506 binding protein 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643880","summary":null,"start":66744561,"end":66745929,"strand":-1,"description":"FK506 binding protein 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50377]"}, {"versioned_ensembl_gene_id":"ENSG00000160963.13","gene_symbol":"COL26A1","gene_name":"collagen type XXVI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:18038]","synonyms":"Emu2,EMID2,EMI6","biotype":"protein_coding","ncbi_id":"136227","summary":"This gene encodes a protein containing an emilin domain and two collagen stretches. This gene may be associated with aspirin-intolerant asthma. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":101362820,"end":101559024,"strand":1,"description":"collagen type XXVI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:18038]"}, {"versioned_ensembl_gene_id":"ENSG00000269952.1","gene_symbol":"AL117336.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35210416,"end":35210750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126106.13","gene_symbol":"TMEM53","gene_name":"transmembrane protein 53 [Source:HGNC Symbol;Acc:HGNC:26186]","synonyms":"NET4,FLJ22353","biotype":"protein_coding","ncbi_id":"79639","summary":null,"start":44635238,"end":44674555,"strand":-1,"description":"transmembrane protein 53 [Source:HGNC Symbol;Acc:HGNC:26186]"}, {"versioned_ensembl_gene_id":"ENSG00000172016.15","gene_symbol":"REG3A","gene_name":"regenerating family member 3 alpha [Source:HGNC Symbol;Acc:HGNC:8601]","synonyms":"REG3,REG-III,PBCGF,PAP1,PAP,HIP","biotype":"protein_coding","ncbi_id":"5068","summary":"This gene encodes a pancreatic secretory protein that may be involved in cell proliferation or differentiation. It has similarity to the C-type lectin superfamily. The enhanced expression of this gene is observed during pancreatic inflammation and liver carcinogenesis. The mature protein also functions as an antimicrobial protein with antibacterial activity. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Nov 2014]","start":79157003,"end":79159753,"strand":-1,"description":"regenerating family member 3 alpha [Source:HGNC Symbol;Acc:HGNC:8601]"}, {"versioned_ensembl_gene_id":"ENSG00000224731.1","gene_symbol":"AC016716.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80028012,"end":80030551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012963.14","gene_symbol":"UBR7","gene_name":"ubiquitin protein ligase E3 component n-recognin 7 (putative) [Source:HGNC Symbol;Acc:HGNC:20344]","synonyms":"C14orf130","biotype":"protein_coding","ncbi_id":"55148","summary":"This gene encodes a UBR box-containing protein that belongs to the E3 ubiquitin ligase family. The protein also contains a plant homeodomain (PHD) in the C-terminus. In mammals, the encoded protein recognizes N-degrons, the destabilizing N-terminal residues of short-lived proteins, which results in ubiquitinylation, and proteolysis via the proteasome. [provided by RefSeq, Jul 2016]","start":93207056,"end":93229215,"strand":1,"description":"ubiquitin protein ligase E3 component n-recognin 7 (putative) [Source:HGNC Symbol;Acc:HGNC:20344]"}, {"versioned_ensembl_gene_id":"ENSG00000184385.2","gene_symbol":"UMODL1-AS1","gene_name":"UMODL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23821]","synonyms":"FLJ33471,C21orf128","biotype":"sense_overlapping","ncbi_id":"150147","summary":null,"start":42102134,"end":42108534,"strand":-1,"description":"UMODL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23821]"}, {"versioned_ensembl_gene_id":"ENSG00000109686.17","gene_symbol":"SH3D19","gene_name":"SH3 domain containing 19 [Source:HGNC Symbol;Acc:HGNC:30418]","synonyms":"SH3P19,Kryn,EVE1,Eve-1,EBP,DKFZp434D0215","biotype":"protein_coding","ncbi_id":"152503","summary":"This gene encodes a multiple SH3 domain-containing protein, which interacts with other proteins, such as EBP and members of ADAM family, via the SH3 domains. This protein may be involved in suppression of Ras-induced cellular transformation and Ras-mediated activation of ELK1 by EBP, and regulation of ADAM proteins in the signaling of EGFR-ligand shedding. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":151102751,"end":151325632,"strand":-1,"description":"SH3 domain containing 19 [Source:HGNC Symbol;Acc:HGNC:30418]"}, {"versioned_ensembl_gene_id":"ENSG00000181234.9","gene_symbol":"TMEM132C","gene_name":"transmembrane protein 132C [Source:HGNC Symbol;Acc:HGNC:25436]","synonyms":"PPP1R152,DKFZp761O2018","biotype":"protein_coding","ncbi_id":"92293","summary":null,"start":128267403,"end":128707915,"strand":1,"description":"transmembrane protein 132C [Source:HGNC Symbol;Acc:HGNC:25436]"}, {"versioned_ensembl_gene_id":"ENSG00000244743.1","gene_symbol":"AC087588.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32863118,"end":32863433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129845.5","gene_symbol":"TTTY1","gene_name":"testis-specific transcript, Y-linked 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14022]","synonyms":"TTY1,NCRNA00033,LINC00033","biotype":"lincRNA","ncbi_id":"50858","summary":null,"start":9753156,"end":9774289,"strand":-1,"description":"testis-specific transcript, Y-linked 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14022]"}, {"versioned_ensembl_gene_id":"ENSG00000198585.11","gene_symbol":"NUDT16","gene_name":"nudix hydrolase 16 [Source:HGNC Symbol;Acc:HGNC:26442]","synonyms":"FLJ31265","biotype":"protein_coding","ncbi_id":"131870","summary":null,"start":131381671,"end":131388830,"strand":1,"description":"nudix hydrolase 16 [Source:HGNC Symbol;Acc:HGNC:26442]"}, {"versioned_ensembl_gene_id":"ENSG00000125498.19","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769811,"end":54784322,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000129484.13","gene_symbol":"PARP2","gene_name":"poly(ADP-ribose) polymerase 2 [Source:HGNC Symbol;Acc:HGNC:272]","synonyms":"ADPRTL2","biotype":"protein_coding","ncbi_id":"10038","summary":"This gene encodes poly(ADP-ribosyl)transferase-like 2 protein, which contains a catalytic domain and is capable of catalyzing a poly(ADP-ribosyl)ation reaction. This protein has a catalytic domain which is homologous to that of poly (ADP-ribosyl) transferase, but lacks an N-terminal DNA binding domain which activates the C-terminal catalytic domain of poly (ADP-ribosyl) transferase. The basic residues within the N-terminal region of this protein may bear potential DNA-binding properties, and may be involved in the nuclear and/or nucleolar targeting of the protein. Two alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jul 2008]","start":20343582,"end":20357905,"strand":1,"description":"poly(ADP-ribose) polymerase 2 [Source:HGNC Symbol;Acc:HGNC:272]"}, {"versioned_ensembl_gene_id":"ENSG00000107938.17","gene_symbol":"EDRF1","gene_name":"erythroid differentiation regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:24640]","synonyms":"FLJ21617,DKFZp586F1019,C10orf137","biotype":"protein_coding","ncbi_id":"26098","summary":"This gene may play a role in erythroid cell differentiation. The encoded protein inhibits DNA binding of the erythroid transcription factor GATA-1 and may regulate the expression of alpha-globin and gamma-globin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":125719515,"end":125764143,"strand":1,"description":"erythroid differentiation regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:24640]"}, {"versioned_ensembl_gene_id":"ENSG00000177464.4","gene_symbol":"GPR4","gene_name":"G protein-coupled receptor 4 [Source:HGNC Symbol;Acc:HGNC:4497]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2828","summary":null,"start":45589764,"end":45602208,"strand":-1,"description":"G protein-coupled receptor 4 [Source:HGNC Symbol;Acc:HGNC:4497]"}, {"versioned_ensembl_gene_id":"ENSG00000166250.11","gene_symbol":"CLMP","gene_name":"CXADR like membrane protein [Source:HGNC Symbol;Acc:HGNC:24039]","synonyms":"FLJ22415,ASAM,ACAM","biotype":"protein_coding","ncbi_id":"79827","summary":"This gene encodes a type I transmembrane protein that is localized to junctional complexes between endothelial and epithelial cells and may have a role in cell-cell adhesion. Expression of this gene in white adipose tissue is implicated in adipocyte maturation and development of obesity. This gene is also essential for normal intestinal development and mutations in the gene are associated with congenital short bowel syndrome. [provided by RefSeq, Aug 2015]","start":123069865,"end":123195281,"strand":-1,"description":"CXADR like membrane protein [Source:HGNC Symbol;Acc:HGNC:24039]"}, {"versioned_ensembl_gene_id":"ENSG00000254272.1","gene_symbol":"AC087854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22492631,"end":22493044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278409.1","gene_symbol":"CU467002.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54362810,"end":54366855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234902.6","gene_symbol":"AC007879.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207186717,"end":207236066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173083.14","gene_symbol":"HPSE","gene_name":"heparanase [Source:HGNC Symbol;Acc:HGNC:5164]","synonyms":"HSE1,HPSE1,HPA","biotype":"protein_coding","ncbi_id":"10855","summary":"Heparan sulfate proteoglycans are major components of the basement membrane and extracellular matrix. The protein encoded by this gene is an enzyme that cleaves heparan sulfate proteoglycans to permit cell movement through remodeling of the extracellular matrix. In addition, this cleavage can release bioactive molecules from the extracellular matrix. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":83292461,"end":83335153,"strand":-1,"description":"heparanase [Source:HGNC Symbol;Acc:HGNC:5164]"}, {"versioned_ensembl_gene_id":"ENSG00000280160.1","gene_symbol":"AC135050.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31093727,"end":31095944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136059.14","gene_symbol":"VILL","gene_name":"villin like [Source:HGNC Symbol;Acc:HGNC:30906]","synonyms":null,"biotype":"protein_coding","ncbi_id":"50853","summary":"The protein encoded by this gene belongs to the villin/gelsolin family. It contains 6 gelsolin-like repeats and a headpiece domain. It may play a role in actin-bundling. [provided by RefSeq, Jul 2008]","start":37988059,"end":38007188,"strand":1,"description":"villin like [Source:HGNC Symbol;Acc:HGNC:30906]"}, {"versioned_ensembl_gene_id":"ENSG00000283692.1","gene_symbol":"Z96074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137573752,"end":137981763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282481.1","gene_symbol":"AC100810.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1761552,"end":1764146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224525.2","gene_symbol":"AL591686.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":242203555,"end":242210827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102924.11","gene_symbol":"CBLN1","gene_name":"cerebellin 1 precursor [Source:HGNC Symbol;Acc:HGNC:1543]","synonyms":null,"biotype":"protein_coding","ncbi_id":"869","summary":"This gene encodes a cerebellum-specific precursor protein, precerebellin, with similarity to the globular (non-collagen-like) domain of complement component C1qB. Precerebellin is processed to give rise to several derivatives, including the hexadecapeptide, cerebellin, which is highly enriched in postsynaptic structures of Purkinje cells. Cerebellin has also been found in human and rat adrenals, where it has been shown to enhance the secretory activity of this gland. [provided by RefSeq, Aug 2008]","start":49277917,"end":49281831,"strand":-1,"description":"cerebellin 1 precursor [Source:HGNC Symbol;Acc:HGNC:1543]"}, {"versioned_ensembl_gene_id":"ENSG00000259473.1","gene_symbol":"LINC02205","gene_name":"long intergenic non-protein coding RNA 2205 [Source:HGNC Symbol;Acc:HGNC:53071]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370880","summary":null,"start":70503907,"end":70505928,"strand":-1,"description":"long intergenic non-protein coding RNA 2205 [Source:HGNC Symbol;Acc:HGNC:53071]"}, {"versioned_ensembl_gene_id":"ENSG00000278834.1","gene_symbol":"AC073508.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40648300,"end":40649718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230921.1","gene_symbol":"HAO2-IT1","gene_name":"HAO2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41342]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874270","summary":null,"start":119368946,"end":119370331,"strand":1,"description":"HAO2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41342]"}, {"versioned_ensembl_gene_id":"ENSG00000275993.2","gene_symbol":"CU639417.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6111134,"end":6123739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249609.1","gene_symbol":"AC080188.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168828919,"end":168832937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279045.1","gene_symbol":"AP003400.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89548130,"end":89548795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197576.13","gene_symbol":"HOXA4","gene_name":"homeobox A4 [Source:HGNC Symbol;Acc:HGNC:5105]","synonyms":"HOX1D,HOX1","biotype":"protein_coding","ncbi_id":"3201","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":27128507,"end":27130799,"strand":-1,"description":"homeobox A4 [Source:HGNC Symbol;Acc:HGNC:5105]"}, {"versioned_ensembl_gene_id":"ENSG00000278661.1","gene_symbol":"TRAJ37","gene_name":"T-cell receptor alpha joining 37 [Source:HGNC Symbol;Acc:HGNC:12067]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28718","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22503750,"end":22503814,"strand":1,"description":"T-cell receptor alpha joining 37 [Source:HGNC Symbol;Acc:HGNC:12067]"}, {"versioned_ensembl_gene_id":"ENSG00000282787.1","gene_symbol":"AL157888.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125162379,"end":125162971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230068.2","gene_symbol":"CDC42-IT1","gene_name":"CDC42 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41317]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874292","summary":null,"start":22059197,"end":22064199,"strand":1,"description":"CDC42 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41317]"}, {"versioned_ensembl_gene_id":"ENSG00000224727.1","gene_symbol":"FCF1P7","gene_name":"FCF1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44619]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422536","summary":null,"start":243267257,"end":243268119,"strand":-1,"description":"FCF1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44619]"}, {"versioned_ensembl_gene_id":"ENSG00000163792.6","gene_symbol":"TCF23","gene_name":"transcription factor 23 [Source:HGNC Symbol;Acc:HGNC:18602]","synonyms":"bHLHa24,OUT","biotype":"protein_coding","ncbi_id":"150921","summary":"The gene encodes a member of the basic helix-loop-helix transcription factor family. Studies of the orthologous gene in mouse have shown the encoded protein does not bind DNA but may negatively regulate other basic helix-loop-helix factors via the formation of a functionally inactive heterodimeric complex. [provided by RefSeq, May 2010]","start":27149004,"end":27156974,"strand":1,"description":"transcription factor 23 [Source:HGNC Symbol;Acc:HGNC:18602]"}, {"versioned_ensembl_gene_id":"ENSG00000198093.10","gene_symbol":"ZNF649","gene_name":"zinc finger protein 649 [Source:HGNC Symbol;Acc:HGNC:25741]","synonyms":"FLJ12644","biotype":"protein_coding","ncbi_id":"65251","summary":null,"start":51889224,"end":51905040,"strand":-1,"description":"zinc finger protein 649 [Source:HGNC Symbol;Acc:HGNC:25741]"}, {"versioned_ensembl_gene_id":"ENSG00000227138.1","gene_symbol":"AL161788.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10777357,"end":10777525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278266.1","gene_symbol":"AC079949.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127147149,"end":127150081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258934.1","gene_symbol":"AL356800.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42807378,"end":42808112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148606.12","gene_symbol":"POLR3A","gene_name":"RNA polymerase III subunit A [Source:HGNC Symbol;Acc:HGNC:30074]","synonyms":"RPC155,RPC1,hRPC155","biotype":"protein_coding","ncbi_id":"11128","summary":"The protein encoded by this gene is the catalytic component of RNA polymerase III, which synthesizes small RNAs. The encoded protein also acts as a sensor to detect foreign DNA and trigger an innate immune response. [provided by RefSeq, Aug 2011]","start":77969251,"end":78029545,"strand":-1,"description":"RNA polymerase III subunit A [Source:HGNC Symbol;Acc:HGNC:30074]"}, {"versioned_ensembl_gene_id":"ENSG00000236864.1","gene_symbol":"AC068295.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187932764,"end":187946221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234163.1","gene_symbol":"MTND4LP11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42245]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075238","summary":null,"start":33023368,"end":33023647,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42245]"}, {"versioned_ensembl_gene_id":"ENSG00000224339.1","gene_symbol":"AL121578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37945884,"end":37946775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164326.4","gene_symbol":"CARTPT","gene_name":"CART prepropeptide [Source:HGNC Symbol;Acc:HGNC:24323]","synonyms":"CART","biotype":"protein_coding","ncbi_id":"9607","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple biologically active peptides. These peptides play a role in appetite, energy balance, maintenance of body weight, reward and addiction, and the stress response. Expression of a similar gene transcript in rodents is upregulated following administration of cocaine and amphetamine. Mutations in this gene are associated with susceptibility to obesity in humans. [provided by RefSeq, Feb 2016]","start":71719163,"end":71721048,"strand":1,"description":"CART prepropeptide [Source:HGNC Symbol;Acc:HGNC:24323]"}, {"versioned_ensembl_gene_id":"ENSG00000280235.1","gene_symbol":"AC139494.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69659867,"end":69661133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196970.8","gene_symbol":"NXF4","gene_name":"nuclear RNA export factor 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8074]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"55999","summary":null,"start":102549965,"end":102571695,"strand":1,"description":"nuclear RNA export factor 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:8074]"}, {"versioned_ensembl_gene_id":"ENSG00000230279.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31562799,"end":31565069,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000279144.1","gene_symbol":"AC099667.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52848085,"end":52848553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250243.2","gene_symbol":"AC110296.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21304542,"end":21316485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259012.2","gene_symbol":"MTCYBP27","gene_name":"mitochondrially encoded cytochrome b pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:51993]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075133","summary":null,"start":84176419,"end":84177088,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:51993]"}, {"versioned_ensembl_gene_id":"ENSG00000237904.2","gene_symbol":"BX284632.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65798726,"end":65799124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237408.1","gene_symbol":"ART2BP","gene_name":"ADP-ribosyltransferase 2B, pseudogene [Source:HGNC Symbol;Acc:HGNC:51489]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481723","summary":null,"start":72478221,"end":72479237,"strand":1,"description":"ADP-ribosyltransferase 2B, pseudogene [Source:HGNC Symbol;Acc:HGNC:51489]"}, {"versioned_ensembl_gene_id":"ENSG00000226566.2","gene_symbol":"AL390962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103361952,"end":103429892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260828.1","gene_symbol":"AC018552.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57603137,"end":57603697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251557.2","gene_symbol":"HNRNPKP3","gene_name":"heterogeneous nuclear ribonucleoprotein K pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42376]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"399881","summary":null,"start":43120762,"end":43269393,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein K pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42376]"}, {"versioned_ensembl_gene_id":"ENSG00000231436.1","gene_symbol":"RBMY3AP","gene_name":"RNA binding motif protein, Y-linked, family 3, member A pseudogene [Source:HGNC Symbol;Acc:HGNC:23286]","synonyms":"SPATA14,RBMY4P,RBMY3P","biotype":"unprocessed_pseudogene","ncbi_id":"64593","summary":null,"start":9610571,"end":9621276,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 3, member A pseudogene [Source:HGNC Symbol;Acc:HGNC:23286]"}, {"versioned_ensembl_gene_id":"ENSG00000231906.1","gene_symbol":"AC016397.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48546472,"end":48546713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215186.6","gene_symbol":"GOLGA6B","gene_name":"golgin A6 family member B [Source:HGNC Symbol;Acc:HGNC:32205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55889","summary":"This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, which are greater than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosomal rearrangements that underlie genomic disease. This gene is a member of the golgin gene family, whose protein products localize to the Golgi apparatus. The majority of the related gene copies are thought to be transcribed pseudogenes. It is not known whether this gene is a pseudogene or if it encodes a golgin protein. [provided by RefSeq, Jul 2008]","start":72654738,"end":72666394,"strand":1,"description":"golgin A6 family member B [Source:HGNC Symbol;Acc:HGNC:32205]"}, {"versioned_ensembl_gene_id":"ENSG00000172270.18","gene_symbol":"BSG","gene_name":"basigin (Ok blood group) [Source:HGNC Symbol;Acc:HGNC:1116]","synonyms":"OK,EMMPRIN,CD147","biotype":"protein_coding","ncbi_id":"682","summary":"The protein encoded by this gene, basigin, is a plasma membrane protein that is important in spermatogenesis, embryo implantation, neural network formation, and tumor progression. Basigin is also a member of the immunoglobulin superfamily, ubiquitously expressed in various tissues. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2020]","start":571277,"end":583493,"strand":1,"description":"basigin (Ok blood group) [Source:HGNC Symbol;Acc:HGNC:1116]"}, {"versioned_ensembl_gene_id":"ENSG00000260144.1","gene_symbol":"AC100827.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72605183,"end":72612326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261243.1","gene_symbol":"AC022165.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84495599,"end":84497495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159208.15","gene_symbol":"CIART","gene_name":"circadian associated repressor of transcription [Source:HGNC Symbol;Acc:HGNC:25200]","synonyms":"C1orf51,BC017397","biotype":"protein_coding","ncbi_id":"148523","summary":null,"start":150282543,"end":150287093,"strand":1,"description":"circadian associated repressor of transcription [Source:HGNC Symbol;Acc:HGNC:25200]"}, {"versioned_ensembl_gene_id":"ENSG00000169129.14","gene_symbol":"AFAP1L2","gene_name":"actin filament associated protein 1 like 2 [Source:HGNC Symbol;Acc:HGNC:25901]","synonyms":"XB130,KIAA1914,FLJ14564,Em:AC005383.4","biotype":"protein_coding","ncbi_id":"84632","summary":null,"start":114294824,"end":114404756,"strand":-1,"description":"actin filament associated protein 1 like 2 [Source:HGNC Symbol;Acc:HGNC:25901]"}, {"versioned_ensembl_gene_id":"ENSG00000154743.17","gene_symbol":"TSEN2","gene_name":"tRNA splicing endonuclease subunit 2 [Source:HGNC Symbol;Acc:HGNC:28422]","synonyms":"SEN2L,SEN2,MGC2776","biotype":"protein_coding","ncbi_id":"80746","summary":"This gene encodes one of the subunits of the tRNA splicing endonuclease. This endonuclease catalyzes the first step in RNA splicing which is the removal of introns. Mutations in this gene have been associated with pontocerebellar hypoplasia type 2. A pseudogene has been identified on chromosome 4. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2009]","start":12484432,"end":12539623,"strand":1,"description":"tRNA splicing endonuclease subunit 2 [Source:HGNC Symbol;Acc:HGNC:28422]"}, {"versioned_ensembl_gene_id":"ENSG00000227961.1","gene_symbol":"CR759870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582464,"end":29582981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232218.1","gene_symbol":"AL021937.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32386668,"end":32386868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135960.9","gene_symbol":"EDAR","gene_name":"ectodysplasin A receptor [Source:HGNC Symbol;Acc:HGNC:2895]","synonyms":"Edar,EDA3,EDA1R,ED5,ED3,ED1R,DL","biotype":"protein_coding","ncbi_id":"10913","summary":"This gene encodes a member of the tumor necrosis factor receptor family. The encoded transmembrane protein is a receptor for the soluble ligand ectodysplasin A, and can activate the nuclear factor-kappaB, JNK, and caspase-independent cell death pathways. It is required for the development of hair, teeth, and other ectodermal derivatives. Mutations in this gene result in autosomal dominant and recessive forms of hypohidrotic ectodermal dysplasia. [provided by RefSeq, Jul 2008]","start":108894471,"end":108989372,"strand":-1,"description":"ectodysplasin A receptor [Source:HGNC Symbol;Acc:HGNC:2895]"}, {"versioned_ensembl_gene_id":"ENSG00000223573.6","gene_symbol":"TINCR","gene_name":"tissue differentiation-inducing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:14607]","synonyms":"PLAC2,onco-lncRNA-16,NCRNA00036,LINC00036,FLJ90734","biotype":"protein_coding","ncbi_id":"257000","summary":"This gene produces a spliced long non-coding RNA that binds RNAs. This transcript interacts with staufen-1 protein to regulate the stability of mRNAs for genes involved in the differentiation of epidermal tissue. Variation in this gene may be associated with cancer progression. [provided by RefSeq, Aug 2017]","start":5558167,"end":5568034,"strand":-1,"description":"tissue differentiation-inducing non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:14607]"}, {"versioned_ensembl_gene_id":"ENSG00000230902.1","gene_symbol":"FAM204CP","gene_name":"family with sequence similarity 204 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:42012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420916","summary":null,"start":75688556,"end":75689197,"strand":-1,"description":"family with sequence similarity 204 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:42012]"}, {"versioned_ensembl_gene_id":"ENSG00000168421.12","gene_symbol":"RHOH","gene_name":"ras homolog family member H [Source:HGNC Symbol;Acc:HGNC:686]","synonyms":"TTF,RhoH,ARHH","biotype":"protein_coding","ncbi_id":"399","summary":"The protein encoded by this gene is a member of the Ras superfamily of guanosine triphosphate (GTP)-metabolizing enzymes. The encoded protein is expressed in hematopoietic cells, where it functions as a negative regulator of cell growth and survival. This gene may be hypermutated or misexpressed in leukemias and lymphomas. Chromosomal translocations in non-Hodgkin's lymphoma occur between this locus and B-cell CLL/lymphoma 6 (BCL6) on chromosome 3, leading to the production of fusion transcripts. Alternative splicing in the 5' untranslated region results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2013]","start":40191053,"end":40246967,"strand":1,"description":"ras homolog family member H [Source:HGNC Symbol;Acc:HGNC:686]"}, {"versioned_ensembl_gene_id":"ENSG00000261613.2","gene_symbol":"AC093525.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2554060,"end":2556060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256221.1","gene_symbol":"AC244502.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22332922,"end":22334685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228662.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31605067,"end":31606582,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000258742.5","gene_symbol":"AL117192.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92886352,"end":92893506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226733.2","gene_symbol":"AL138826.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50093616,"end":50181007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197888.2","gene_symbol":"UGT2B17","gene_name":"UDP glucuronosyltransferase family 2 member B17 [Source:HGNC Symbol;Acc:HGNC:12547]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7367","summary":"This gene encodes a member of the uridine diphosphoglucuronosyltransferase protein family. The encoded enzyme catalyzes the transfer of glucuronic acid from uridine diphosphoglucuronic acid to a diverse array of substrates including steroid hormones and lipid-soluble drugs. This process, known as glucuronidation, is an intermediate step in the metabolism of steroids. Copy number variation in this gene is associated with susceptibility to osteoporosis.[provided by RefSeq, Apr 2010]","start":68537184,"end":68568527,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B17 [Source:HGNC Symbol;Acc:HGNC:12547]"}, {"versioned_ensembl_gene_id":"ENSG00000279171.1","gene_symbol":"AC006065.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126677262,"end":126677806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110367.11","gene_symbol":"DDX6","gene_name":"DEAD-box helicase 6 [Source:HGNC Symbol;Acc:HGNC:2747]","synonyms":"RCK,HLR2","biotype":"protein_coding","ncbi_id":"1656","summary":"This gene encodes a member of the DEAD box protein family. The protein is an RNA helicase found in P-bodies and stress granules, and functions in translation suppression and mRNA degradation. It is required for microRNA-induced gene silencing. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Mar 2012]","start":118747766,"end":118791149,"strand":-1,"description":"DEAD-box helicase 6 [Source:HGNC Symbol;Acc:HGNC:2747]"}, {"versioned_ensembl_gene_id":"ENSG00000198785.4","gene_symbol":"GRIN3A","gene_name":"glutamate ionotropic receptor NMDA type subunit 3A [Source:HGNC Symbol;Acc:HGNC:16767]","synonyms":"GluN3A","biotype":"protein_coding","ncbi_id":"116443","summary":"This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptors, which belong to the superfamily of glutamate-regulated ion channels, and function in physiological and pathological processes in the central nervous system. This subunit shows greater than 90% identity to the corresponding subunit in rat. Studies in the knockout mouse deficient in this subunit suggest that this gene may be involved in the development of synaptic elements by modulating NMDA receptor activity. [provided by RefSeq, Jul 2008]","start":101569353,"end":101738580,"strand":-1,"description":"glutamate ionotropic receptor NMDA type subunit 3A [Source:HGNC Symbol;Acc:HGNC:16767]"}, {"versioned_ensembl_gene_id":"ENSG00000196126.11","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32578769,"end":32589848,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000254750.1","gene_symbol":"CASP1P2","gene_name":"caspase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43776]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440067","summary":null,"start":105063345,"end":105071541,"strand":-1,"description":"caspase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43776]"}, {"versioned_ensembl_gene_id":"ENSG00000236290.1","gene_symbol":"EEF1GP7","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645311","summary":null,"start":52573114,"end":52573816,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44562]"}, {"versioned_ensembl_gene_id":"ENSG00000143603.18","gene_symbol":"KCNN3","gene_name":"potassium calcium-activated channel subfamily N member 3 [Source:HGNC Symbol;Acc:HGNC:6292]","synonyms":"hSK3,SKCA3,KCa2.3","biotype":"protein_coding","ncbi_id":"3782","summary":"Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. This gene belongs to the KCNN family of potassium channels. It encodes an integral membrane protein that forms a voltage-independent calcium-activated channel, which is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene contains two CAG repeat regions in the coding sequence. It was thought that expansion of one or both of these repeats could lead to an increased susceptibility to schizophrenia or bipolar disorder, but studies indicate that this is probably not the case. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":154697455,"end":154870280,"strand":-1,"description":"potassium calcium-activated channel subfamily N member 3 [Source:HGNC Symbol;Acc:HGNC:6292]"}, {"versioned_ensembl_gene_id":"ENSG00000074842.7","gene_symbol":"MYDGF","gene_name":"myeloid derived growth factor [Source:HGNC Symbol;Acc:HGNC:16948]","synonyms":"SF20,R33729_1,IL27w,IL27,IL25,IL-27,IL-25,C19orf10","biotype":"protein_coding","ncbi_id":"56005","summary":"The protein encoded by this gene was previously thought to support proliferation of lymphoid cells and was considered an interleukin. However, this activity has not been reproducible and the function of this protein is currently unknown. [provided by RefSeq, Jul 2008]","start":4641374,"end":4670370,"strand":-1,"description":"myeloid derived growth factor [Source:HGNC Symbol;Acc:HGNC:16948]"}, {"versioned_ensembl_gene_id":"ENSG00000164649.19","gene_symbol":"CDCA7L","gene_name":"cell division cycle associated 7 like [Source:HGNC Symbol;Acc:HGNC:30777]","synonyms":"RAM2,R1,JPO2","biotype":"protein_coding","ncbi_id":"55536","summary":null,"start":21900900,"end":21946084,"strand":-1,"description":"cell division cycle associated 7 like [Source:HGNC Symbol;Acc:HGNC:30777]"}, {"versioned_ensembl_gene_id":"ENSG00000272861.1","gene_symbol":"AC012360.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105249404,"end":105249794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176007.10","gene_symbol":"FAM220BP","gene_name":"family with sequence similarity 220 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:23678]","synonyms":"C9orf51,bA392E22.4","biotype":"processed_pseudogene","ncbi_id":"647044","summary":null,"start":38527097,"end":38527912,"strand":1,"description":"family with sequence similarity 220 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:23678]"}, {"versioned_ensembl_gene_id":"ENSG00000250708.1","gene_symbol":"LINC02269","gene_name":"long intergenic non-protein coding RNA 2269 [Source:HGNC Symbol;Acc:HGNC:53184]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928478","summary":null,"start":173897252,"end":173929525,"strand":1,"description":"long intergenic non-protein coding RNA 2269 [Source:HGNC Symbol;Acc:HGNC:53184]"}, {"versioned_ensembl_gene_id":"ENSG00000251525.6","gene_symbol":"TCP11X3P","gene_name":"t-complex 11 family, X-linked 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:48370]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106481605","summary":null,"start":102173100,"end":102185021,"strand":1,"description":"t-complex 11 family, X-linked 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:48370]"}, {"versioned_ensembl_gene_id":"ENSG00000155729.12","gene_symbol":"KCTD18","gene_name":"potassium channel tetramerization domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26446]","synonyms":"FLJ31322,6530404F10Rik,FLJ37818","biotype":"protein_coding","ncbi_id":"130535","summary":null,"start":200488952,"end":200519784,"strand":-1,"description":"potassium channel tetramerization domain containing 18 [Source:HGNC Symbol;Acc:HGNC:26446]"}, {"versioned_ensembl_gene_id":"ENSG00000228820.2","gene_symbol":"RPSAP1","gene_name":"ribosomal protein SA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16560]","synonyms":"LAMR1P1,LAMR1P,dJ1193N1.1","biotype":"processed_pseudogene","ncbi_id":"170529","summary":null,"start":51130788,"end":51131667,"strand":-1,"description":"ribosomal protein SA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16560]"}, {"versioned_ensembl_gene_id":"ENSG00000178522.14","gene_symbol":"AMBN","gene_name":"ameloblastin [Source:HGNC Symbol;Acc:HGNC:452]","synonyms":null,"biotype":"protein_coding","ncbi_id":"258","summary":"This gene encodes the nonamelogenin enamel matrix protein ameloblastin. The encoded protein may be important in enamel matrix formation and mineralization. This gene is located in the calcium-binding phosphoprotein gene cluster on chromosome 4. Mutations in this gene may be associated with dentinogenesis imperfect and autosomal dominant amylogenesis imperfect. [provided by RefSeq, Aug 2011]","start":70592256,"end":70607288,"strand":1,"description":"ameloblastin [Source:HGNC Symbol;Acc:HGNC:452]"}, {"versioned_ensembl_gene_id":"ENSG00000279942.1","gene_symbol":"AL353597.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37567716,"end":37571460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164362.18","gene_symbol":"TERT","gene_name":"telomerase reverse transcriptase [Source:HGNC Symbol;Acc:HGNC:11730]","synonyms":"TRT,TP2,TCS1,hEST2,EST2","biotype":"protein_coding","ncbi_id":"7015","summary":"Telomerase is a ribonucleoprotein polymerase that maintains telomere ends by addition of the telomere repeat TTAGGG. The enzyme consists of a protein component with reverse transcriptase activity, encoded by this gene, and an RNA component which serves as a template for the telomere repeat. Telomerase expression plays a role in cellular senescence, as it is normally repressed in postnatal somatic cells resulting in progressive shortening of telomeres. Deregulation of telomerase expression in somatic cells may be involved in oncogenesis. Studies in mouse suggest that telomerase also participates in chromosomal repair, since de novo synthesis of telomere repeats may occur at double-stranded breaks. Alternatively spliced variants encoding different isoforms of telomerase reverse transcriptase have been identified; the full-length sequence of some variants has not been determined. Alternative splicing at this locus is thought to be one mechanism of regulation of telomerase activity. [provided by RefSeq, Jul 2008]","start":1253147,"end":1295069,"strand":-1,"description":"telomerase reverse transcriptase [Source:HGNC Symbol;Acc:HGNC:11730]"}, {"versioned_ensembl_gene_id":"ENSG00000123353.9","gene_symbol":"ORMDL2","gene_name":"ORMDL sphingolipid biosynthesis regulator 2 [Source:HGNC Symbol;Acc:HGNC:16037]","synonyms":"MSTP095,MST095,HSPC160,adoplin-2","biotype":"protein_coding","ncbi_id":"29095","summary":null,"start":55817919,"end":55821879,"strand":1,"description":"ORMDL sphingolipid biosynthesis regulator 2 [Source:HGNC Symbol;Acc:HGNC:16037]"}, {"versioned_ensembl_gene_id":"ENSG00000225906.1","gene_symbol":"AP000949.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22882582,"end":22884000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244249.1","gene_symbol":"AC063955.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159386756,"end":159387440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160710.15","gene_symbol":"ADAR","gene_name":"adenosine deaminase, RNA specific [Source:HGNC Symbol;Acc:HGNC:225]","synonyms":"ADAR1,IFI4,G1P1","biotype":"protein_coding","ncbi_id":"103","summary":"This gene encodes the enzyme responsible for RNA editing by site-specific deamination of adenosines. This enzyme destabilizes double-stranded RNA through conversion of adenosine to inosine. Mutations in this gene have been associated with dyschromatosis symmetrica hereditaria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":154582062,"end":154627999,"strand":-1,"description":"adenosine deaminase, RNA specific [Source:HGNC Symbol;Acc:HGNC:225]"}, {"versioned_ensembl_gene_id":"ENSG00000272912.1","gene_symbol":"AL356608.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102914585,"end":102915404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180720.7","gene_symbol":"CHRM4","gene_name":"cholinergic receptor muscarinic 4 [Source:HGNC Symbol;Acc:HGNC:1953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1132","summary":"The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The clinical implications of this receptor are unknown; however, mouse studies link its function to adenylyl cyclase inhibition. [provided by RefSeq, Jul 2008]","start":46385098,"end":46386608,"strand":-1,"description":"cholinergic receptor muscarinic 4 [Source:HGNC Symbol;Acc:HGNC:1953]"}, {"versioned_ensembl_gene_id":"ENSG00000230430.4","gene_symbol":"USP17L25","gene_name":"ubiquitin specific peptidase 17-like family member 25 [Source:HGNC Symbol;Acc:HGNC:44452]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728373","summary":null,"start":9329911,"end":9331862,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 25 [Source:HGNC Symbol;Acc:HGNC:44452]"}, {"versioned_ensembl_gene_id":"ENSG00000121895.7","gene_symbol":"TMEM156","gene_name":"transmembrane protein 156 [Source:HGNC Symbol;Acc:HGNC:26260]","synonyms":"FLJ23235","biotype":"protein_coding","ncbi_id":"80008","summary":null,"start":38966744,"end":39032922,"strand":-1,"description":"transmembrane protein 156 [Source:HGNC Symbol;Acc:HGNC:26260]"}, {"versioned_ensembl_gene_id":"ENSG00000157404.15","gene_symbol":"KIT","gene_name":"KIT proto-oncogene receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6342]","synonyms":"SCFR,PBT,CD117,C-Kit","biotype":"protein_coding","ncbi_id":"3815","summary":"This gene encodes a receptor tyrosine kinase. This gene was initially identified as a homolog of the feline sarcoma viral oncogene v-kit and is often referred to as proto-oncogene c-Kit. The canonical form of this glycosylated transmembrane protein has an N-terminal extracellular region with five immunoglobulin-like domains, a transmembrane region, and an intracellular tyrosine kinase domain at the C-terminus. Upon activation by its cytokine ligand, stem cell factor (SCF), this protein phosphorylates multiple intracellular proteins that play a role in in the proliferation, differentiation, migration and apoptosis of many cell types and thereby plays an important role in hematopoiesis, stem cell maintenance, gametogenesis, melanogenesis, and in mast cell development, migration and function. This protein can be a membrane-bound or soluble protein. Mutations in this gene are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous leukemia, and piebaldism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2020]","start":54657918,"end":54740715,"strand":1,"description":"KIT proto-oncogene receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6342]"}, {"versioned_ensembl_gene_id":"ENSG00000271338.1","gene_symbol":"AL591034.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53381519,"end":53382203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184058.13","gene_symbol":"TBX1","gene_name":"T-box 1 [Source:HGNC Symbol;Acc:HGNC:11592]","synonyms":"CATCH22,VCF","biotype":"protein_coding","ncbi_id":"6899","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":19756703,"end":19783593,"strand":1,"description":"T-box 1 [Source:HGNC Symbol;Acc:HGNC:11592]"}, {"versioned_ensembl_gene_id":"ENSG00000250913.2","gene_symbol":"USP17L23","gene_name":"ubiquitin specific peptidase 17-like family member 23 [Source:HGNC Symbol;Acc:HGNC:44451]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101241878","summary":null,"start":9272364,"end":9272914,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 23 [Source:HGNC Symbol;Acc:HGNC:44451]"}, {"versioned_ensembl_gene_id":"ENSG00000267100.1","gene_symbol":"ILF3-AS1","gene_name":"ILF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27115]","synonyms":null,"biotype":"lincRNA","ncbi_id":"147727","summary":null,"start":10651862,"end":10653844,"strand":-1,"description":"ILF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27115]"}, {"versioned_ensembl_gene_id":"ENSG00000100600.14","gene_symbol":"LGMN","gene_name":"legumain [Source:HGNC Symbol;Acc:HGNC:9472]","synonyms":"PRSC1,LGMN1","biotype":"protein_coding","ncbi_id":"5641","summary":"This gene encodes a cysteine protease that has a strict specificity for hydrolysis of asparaginyl bonds. This enzyme may be involved in the processing of bacterial peptides and endogenous proteins for MHC class II presentation in the lysosomal/endosomal systems. Enzyme activation is triggered by acidic pH and appears to be autocatalytic. Protein expression occurs after monocytes differentiate into dendritic cells. A fully mature, active enzyme is produced following lipopolysaccharide expression in mature dendritic cells. Overexpression of this gene may be associated with the majority of solid tumor types. This gene has a pseudogene on chromosome 13. Several alternatively spliced transcript variants have been described, but the biological validity of only two has been determined. These two variants encode the same isoform. [provided by RefSeq, Jul 2008]","start":92703807,"end":92748702,"strand":-1,"description":"legumain [Source:HGNC Symbol;Acc:HGNC:9472]"}, {"versioned_ensembl_gene_id":"ENSG00000219863.5","gene_symbol":"AL034374.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53354715,"end":53355065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271367.1","gene_symbol":"AL034374.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53350158,"end":53350705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100526.19","gene_symbol":"CDKN3","gene_name":"cyclin dependent kinase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:1791]","synonyms":"KAP,CDI1","biotype":"protein_coding","ncbi_id":"1033","summary":"The protein encoded by this gene belongs to the dual specificity protein phosphatase family. It was identified as a cyclin-dependent kinase inhibitor, and has been shown to interact with, and dephosphorylate CDK2 kinase, thus prevent the activation of CDK2 kinase. This gene was reported to be deleted, mutated, or overexpressed in several kinds of cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":54396849,"end":54420218,"strand":1,"description":"cyclin dependent kinase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:1791]"}, {"versioned_ensembl_gene_id":"ENSG00000250745.2","gene_symbol":"USP17L20","gene_name":"ubiquitin specific peptidase 17-like family member 20 [Source:HGNC Symbol;Acc:HGNC:44448]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287441","summary":null,"start":9258124,"end":9260075,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 20 [Source:HGNC Symbol;Acc:HGNC:44448]"}, {"versioned_ensembl_gene_id":"ENSG00000227278.1","gene_symbol":"AL603839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40514461,"end":40515057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283972.1","gene_symbol":"AP000550.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21193360,"end":21203755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262262.1","gene_symbol":"AC026271.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18638019,"end":18638370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272010.1","gene_symbol":"AC100814.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65591850,"end":65592472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233997.5","gene_symbol":"LINC01425","gene_name":"long intergenic non-protein coding RNA 1425 [Source:HGNC Symbol;Acc:HGNC:50733]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927821","summary":null,"start":21746973,"end":21797415,"strand":1,"description":"long intergenic non-protein coding RNA 1425 [Source:HGNC Symbol;Acc:HGNC:50733]"}, {"versioned_ensembl_gene_id":"ENSG00000281920.1","gene_symbol":"AC007389.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65623272,"end":65628424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204929.12","gene_symbol":"AC007389.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":65436711,"end":66084639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248913.1","gene_symbol":"PHBP14","gene_name":"prohibitin pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39293]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873751","summary":null,"start":167648430,"end":167648796,"strand":1,"description":"prohibitin pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39293]"}, {"versioned_ensembl_gene_id":"ENSG00000223911.1","gene_symbol":"AC009480.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147899401,"end":147902956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224007.1","gene_symbol":"AC019070.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148295656,"end":148296679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166233.14","gene_symbol":"ARIH1","gene_name":"ariadne RBR E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:689]","synonyms":"UBCH7BP,HHARI,HARI,ARI","biotype":"protein_coding","ncbi_id":"25820","summary":null,"start":72474326,"end":72602985,"strand":1,"description":"ariadne RBR E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:689]"}, {"versioned_ensembl_gene_id":"ENSG00000104613.11","gene_symbol":"INTS10","gene_name":"integrator complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:25548]","synonyms":"INT10,FLJ10569,C8orf35","biotype":"protein_coding","ncbi_id":"55174","summary":"INTS10 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":19817140,"end":19852083,"strand":1,"description":"integrator complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:25548]"}, {"versioned_ensembl_gene_id":"ENSG00000061492.11","gene_symbol":"WNT8A","gene_name":"Wnt family member 8A [Source:HGNC Symbol;Acc:HGNC:12788]","synonyms":"WNT8D","biotype":"protein_coding","ncbi_id":"7478","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family, and may be implicated in development of early embryos as well as germ cell tumors. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2014]","start":138083892,"end":138092365,"strand":1,"description":"Wnt family member 8A [Source:HGNC Symbol;Acc:HGNC:12788]"}, {"versioned_ensembl_gene_id":"ENSG00000099365.10","gene_symbol":"STX1B","gene_name":"syntaxin 1B [Source:HGNC Symbol;Acc:HGNC:18539]","synonyms":"STX1B2,STX1B1","biotype":"protein_coding","ncbi_id":"112755","summary":"The protein encoded by this gene belongs to a family of proteins thought to play a role in the exocytosis of synaptic vesicles. Vesicle exocytosis releases vesicular contents and is important to various cellular functions. For instance, the secretion of transmitters from neurons plays an important role in synaptic transmission. After exocytosis, the membrane and proteins from the vesicle are retrieved from the plasma membrane through the process of endocytosis. Mutations in this gene have been identified as one cause of fever-associated epilepsy syndromes. A possible link between this gene and Parkinson's disease has also been suggested. [provided by RefSeq, Jan 2015]","start":30989256,"end":31010661,"strand":-1,"description":"syntaxin 1B [Source:HGNC Symbol;Acc:HGNC:18539]"}, {"versioned_ensembl_gene_id":"ENSG00000188895.11","gene_symbol":"MSL1","gene_name":"male specific lethal 1 homolog [Source:HGNC Symbol;Acc:HGNC:27905]","synonyms":"MSL-1,hMSL1,DKFZp686P24239","biotype":"protein_coding","ncbi_id":"339287","summary":null,"start":40122298,"end":40136916,"strand":1,"description":"male specific lethal 1 homolog [Source:HGNC Symbol;Acc:HGNC:27905]"}, {"versioned_ensembl_gene_id":"ENSG00000233481.4","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"protein_coding","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29396107,"end":29397175,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000106397.11","gene_symbol":"PLOD3","gene_name":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 [Source:HGNC Symbol;Acc:HGNC:9083]","synonyms":"LH3","biotype":"protein_coding","ncbi_id":"8985","summary":"The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. [provided by RefSeq, Jul 2008]","start":101205977,"end":101218420,"strand":-1,"description":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 [Source:HGNC Symbol;Acc:HGNC:9083]"}, {"versioned_ensembl_gene_id":"ENSG00000230164.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"MAS1LP,OTTHUMG00000086553","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29475025,"end":29476071,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000170379.19","gene_symbol":"TCAF2","gene_name":"TRPM8 channel associated factor 2 [Source:HGNC Symbol;Acc:HGNC:26878]","synonyms":"GATD9,FLJ40722,FAM139A,FAM115C","biotype":"protein_coding","ncbi_id":"285966","summary":null,"start":143620950,"end":143730409,"strand":1,"description":"TRPM8 channel associated factor 2 [Source:HGNC Symbol;Acc:HGNC:26878]"}, {"versioned_ensembl_gene_id":"ENSG00000238287.1","gene_symbol":"AL603839.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40493157,"end":40508661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237040.6","gene_symbol":"DPH3P2","gene_name":"diphthamide biosynthesis 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38719]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478926","summary":null,"start":155875636,"end":155875885,"strand":1,"description":"diphthamide biosynthesis 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38719]"}, {"versioned_ensembl_gene_id":"ENSG00000172487.4","gene_symbol":"OR8J1","gene_name":"olfactory receptor family 8 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:14855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219477","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56354291,"end":56361511,"strand":1,"description":"olfactory receptor family 8 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:14855]"}, {"versioned_ensembl_gene_id":"ENSG00000231533.1","gene_symbol":"AL078601.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79420297,"end":79421305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251680.5","gene_symbol":"AC008591.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129500361,"end":129905917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198108.3","gene_symbol":"CHSY3","gene_name":"chondroitin sulfate synthase 3 [Source:HGNC Symbol;Acc:HGNC:24293]","synonyms":"CSS3,CHSY-2","biotype":"protein_coding","ncbi_id":"337876","summary":"CSS3 is a glycosyltransferase that has both glucuronyltransferase and N-acetylgalactosaminyltransferase activities (Yada et al., 2003 [PubMed 12907687]).[supplied by OMIM, Mar 2008]","start":129904472,"end":130186634,"strand":1,"description":"chondroitin sulfate synthase 3 [Source:HGNC Symbol;Acc:HGNC:24293]"}, {"versioned_ensembl_gene_id":"ENSG00000227453.1","gene_symbol":"HNRNPA1P63","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:48793]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645436","summary":null,"start":54536796,"end":54537758,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:48793]"}, {"versioned_ensembl_gene_id":"ENSG00000131068.3","gene_symbol":"DEFB118","gene_name":"defensin beta 118 [Source:HGNC Symbol;Acc:HGNC:16196]","synonyms":"DEFB-18,C20orf63,ESC42,dJ1018D12.3","biotype":"protein_coding","ncbi_id":"117285","summary":"This gene encodes a member of the beta subfamily of defensins. Beta-defensins are antimicrobial peptides that protect tissues and organs from infection by a variety of microorganisms. Expression of this gene is regulated by androgen, and the encoded protein binds to sperm and exhibits antibacterial activity against E. coli. This gene is found in a cluster with other beta-defensin genes on the long arm of chromosome 20. [provided by RefSeq, Nov 2014]","start":31368618,"end":31373923,"strand":1,"description":"defensin beta 118 [Source:HGNC Symbol;Acc:HGNC:16196]"}, {"versioned_ensembl_gene_id":"ENSG00000232693.2","gene_symbol":"AC012370.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65373700,"end":65380685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237173.1","gene_symbol":"AC099796.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54524824,"end":54524931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235741.1","gene_symbol":"AC099796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54516412,"end":54517259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248958.2","gene_symbol":"ZSWIM5P3","gene_name":"zinc finger SWIM-type containing 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391697","summary":null,"start":129135926,"end":129139740,"strand":-1,"description":"zinc finger SWIM-type containing 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43770]"}, {"versioned_ensembl_gene_id":"ENSG00000234806.1","gene_symbol":"RPL26P29","gene_name":"ribosomal protein L26 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36135]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131788","summary":null,"start":68424560,"end":68424997,"strand":1,"description":"ribosomal protein L26 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36135]"}, {"versioned_ensembl_gene_id":"ENSG00000227188.1","gene_symbol":"MGAT3-AS1","gene_name":"MGAT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51356]","synonyms":"TapSAKI","biotype":"antisense_RNA","ncbi_id":"104502417","summary":null,"start":39475807,"end":39476822,"strand":-1,"description":"MGAT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51356]"}, {"versioned_ensembl_gene_id":"ENSG00000213077.5","gene_symbol":"FAM106A","gene_name":"family with sequence similarity 106 member A [Source:HGNC Symbol;Acc:HGNC:25682]","synonyms":"FLJ11800","biotype":"protein_coding","ncbi_id":"80039","summary":null,"start":18524566,"end":18526846,"strand":-1,"description":"family with sequence similarity 106 member A [Source:HGNC Symbol;Acc:HGNC:25682]"}, {"versioned_ensembl_gene_id":"ENSG00000238231.2","gene_symbol":"AL512288.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27990158,"end":27990524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102743.14","gene_symbol":"SLC25A15","gene_name":"solute carrier family 25 member 15 [Source:HGNC Symbol;Acc:HGNC:10985]","synonyms":"ORNT1,ORC1,HHH,D13S327","biotype":"protein_coding","ncbi_id":"10166","summary":"This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.[provided by RefSeq, May 2009]","start":40789412,"end":40810111,"strand":1,"description":"solute carrier family 25 member 15 [Source:HGNC Symbol;Acc:HGNC:10985]"}, {"versioned_ensembl_gene_id":"ENSG00000134061.5","gene_symbol":"CD180","gene_name":"CD180 molecule [Source:HGNC Symbol;Acc:HGNC:6726]","synonyms":"RP105,Ly78,LY64","biotype":"protein_coding","ncbi_id":"4064","summary":"CD180 is a cell surface molecule consisting of extracellular leucine-rich repeats (LRR) and a short cytoplasmic tail. The extracellular LRR is associated with a molecule called MD-1 and form the cell surface receptor complex, RP105/MD-1. It belongs to the family of pathogen receptors, Toll-like receptors (TLR). RP105/MD1, by working in concert with TLR4, controls B cell recognition and signaling of lipopolysaccharide (LPS), a membrane constituent of Gram-negative bacteria. [provided by RefSeq, Jul 2008]","start":67179613,"end":67196799,"strand":-1,"description":"CD180 molecule [Source:HGNC Symbol;Acc:HGNC:6726]"}, {"versioned_ensembl_gene_id":"ENSG00000137807.13","gene_symbol":"KIF23","gene_name":"kinesin family member 23 [Source:HGNC Symbol;Acc:HGNC:6392]","synonyms":"MKLP1,MKLP-1,KNSL5","biotype":"protein_coding","ncbi_id":"9493","summary":"The protein encoded by this gene is a member of kinesin-like protein family. This family includes microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. This protein has been shown to cross-bridge antiparallel microtubules and drive microtubule movement in vitro. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":69414246,"end":69448427,"strand":1,"description":"kinesin family member 23 [Source:HGNC Symbol;Acc:HGNC:6392]"}, {"versioned_ensembl_gene_id":"ENSG00000132170.19","gene_symbol":"PPARG","gene_name":"peroxisome proliferator activated receptor gamma [Source:HGNC Symbol;Acc:HGNC:9236]","synonyms":"PPARgamma,PPARG2,PPARG1,NR1C3","biotype":"protein_coding","ncbi_id":"5468","summary":"This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]","start":12287368,"end":12434356,"strand":1,"description":"peroxisome proliferator activated receptor gamma [Source:HGNC Symbol;Acc:HGNC:9236]"}, {"versioned_ensembl_gene_id":"ENSG00000279268.1","gene_symbol":"AC068213.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":65226472,"end":65226697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230459.3","gene_symbol":"AC060773.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77278465,"end":77278774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267321.2","gene_symbol":"LINC02001","gene_name":"long intergenic non-protein coding RNA 2001 [Source:HGNC Symbol;Acc:HGNC:52836]","synonyms":"RP11-1094M14.11","biotype":"lincRNA","ncbi_id":"105371743","summary":null,"start":35568109,"end":35574843,"strand":1,"description":"long intergenic non-protein coding RNA 2001 [Source:HGNC Symbol;Acc:HGNC:52836]"}, {"versioned_ensembl_gene_id":"ENSG00000277745.1","gene_symbol":"H2AFB3","gene_name":"H2A histone family member B3 [Source:HGNC Symbol;Acc:HGNC:14455]","synonyms":"H2AFB","biotype":"protein_coding","ncbi_id":"83740","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the most telomeric copy. [provided by RefSeq, Oct 2015]","start":155459415,"end":155460005,"strand":-1,"description":"H2A histone family member B3 [Source:HGNC Symbol;Acc:HGNC:14455]"}, {"versioned_ensembl_gene_id":"ENSG00000215546.2","gene_symbol":"DKKL1P1","gene_name":"dickkopf-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16593]","synonyms":"DKKL2,dJ854E16.1","biotype":"processed_pseudogene","ncbi_id":"128848","summary":null,"start":31274170,"end":31274867,"strand":1,"description":"dickkopf-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16593]"}, {"versioned_ensembl_gene_id":"ENSG00000236425.1","gene_symbol":"AC069213.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195561215,"end":195561580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233663.1","gene_symbol":"AL161722.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35710911,"end":35711942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240721.2","gene_symbol":"RPS4XP15","gene_name":"ribosomal protein S4X pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36308]","synonyms":"RPS4P15","biotype":"processed_pseudogene","ncbi_id":"100131055","summary":null,"start":87944885,"end":87950819,"strand":1,"description":"ribosomal protein S4X pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36308]"}, {"versioned_ensembl_gene_id":"ENSG00000123179.13","gene_symbol":"EBPL","gene_name":"emopamil binding protein like [Source:HGNC Symbol;Acc:HGNC:18061]","synonyms":"EBRP","biotype":"protein_coding","ncbi_id":"84650","summary":null,"start":49660723,"end":49691475,"strand":-1,"description":"emopamil binding protein like [Source:HGNC Symbol;Acc:HGNC:18061]"}, {"versioned_ensembl_gene_id":"ENSG00000213896.4","gene_symbol":"AC109486.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60429903,"end":60430276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204697.3","gene_symbol":"AL672167.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29262703,"end":29264079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084070.11","gene_symbol":"SMAP2","gene_name":"small ArfGAP2 [Source:HGNC Symbol;Acc:HGNC:25082]","synonyms":"SMAP1L","biotype":"protein_coding","ncbi_id":"64744","summary":null,"start":40344850,"end":40423326,"strand":1,"description":"small ArfGAP2 [Source:HGNC Symbol;Acc:HGNC:25082]"}, {"versioned_ensembl_gene_id":"ENSG00000256814.1","gene_symbol":"AC122688.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125150058,"end":125151394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258468.1","gene_symbol":"OR11G1P","gene_name":"olfactory receptor family 11 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15345]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390438","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20179189,"end":20180156,"strand":1,"description":"olfactory receptor family 11 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15345]"}, {"versioned_ensembl_gene_id":"ENSG00000227529.1","gene_symbol":"CR547123.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076537,"end":29077132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234132.2","gene_symbol":"AL358473.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201031136,"end":201043073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259956.1","gene_symbol":"RBM15B","gene_name":"RNA binding motif protein 15B [Source:HGNC Symbol;Acc:HGNC:24303]","synonyms":"OTT3,HUMAGCGB","biotype":"protein_coding","ncbi_id":"29890","summary":"Members of the SPEN (Split-end) family of proteins, including RBM15B, have repressor function in several signaling pathways and may bind to RNA through interaction with spliceosome components (Hiriart et al., 2005 [PubMed 16129689]).[supplied by OMIM, Feb 2009]","start":51391268,"end":51397908,"strand":1,"description":"RNA binding motif protein 15B [Source:HGNC Symbol;Acc:HGNC:24303]"}, {"versioned_ensembl_gene_id":"ENSG00000226677.3","gene_symbol":"IGBP1P1","gene_name":"immunoglobulin (CD79A) binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19709]","synonyms":"C14orf19","biotype":"processed_pseudogene","ncbi_id":"280655","summary":null,"start":34939324,"end":34940332,"strand":1,"description":"immunoglobulin (CD79A) binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19709]"}, {"versioned_ensembl_gene_id":"ENSG00000186104.10","gene_symbol":"CYP2R1","gene_name":"cytochrome P450 family 2 subfamily R member 1 [Source:HGNC Symbol;Acc:HGNC:20580]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120227","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a microsomal vitamin D hydroxylase that converts vitamin D into the active ligand for the vitamin D receptor. A mutation in this gene has been associated with selective 25-hydroxyvitamin D deficiency. [provided by RefSeq, Jul 2008]","start":14877440,"end":14892252,"strand":-1,"description":"cytochrome P450 family 2 subfamily R member 1 [Source:HGNC Symbol;Acc:HGNC:20580]"}, {"versioned_ensembl_gene_id":"ENSG00000213394.3","gene_symbol":"RPSAP46","gene_name":"ribosomal protein SA pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36082]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652624","summary":null,"start":101203614,"end":101204495,"strand":-1,"description":"ribosomal protein SA pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36082]"}, {"versioned_ensembl_gene_id":"ENSG00000118482.11","gene_symbol":"PHF3","gene_name":"PHD finger protein 3 [Source:HGNC Symbol;Acc:HGNC:8921]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23469","summary":"This gene encodes a member of a PHD finger-containing gene family. This gene may function as a transcription factor and may be involved in glioblastomas development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":63635820,"end":63779336,"strand":1,"description":"PHD finger protein 3 [Source:HGNC Symbol;Acc:HGNC:8921]"}, {"versioned_ensembl_gene_id":"ENSG00000267493.3","gene_symbol":"CIRBP-AS1","gene_name":"CIRBP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28588]","synonyms":"MGC39338,C19orf23","biotype":"antisense_RNA","ncbi_id":"148046","summary":null,"start":1267814,"end":1270241,"strand":-1,"description":"CIRBP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28588]"}, {"versioned_ensembl_gene_id":"ENSG00000121892.14","gene_symbol":"PDS5A","gene_name":"PDS5 cohesin associated factor A [Source:HGNC Symbol;Acc:HGNC:29088]","synonyms":"SCC-112,PIG54,KIAA0648","biotype":"protein_coding","ncbi_id":"23244","summary":"The protein encoded by this gene binds to the cohesin complex and associates with chromatin through most of the cell cycle. The encoded protein may play a role in regulating sister chromatid cohesion during mitosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":39822863,"end":39977956,"strand":-1,"description":"PDS5 cohesin associated factor A [Source:HGNC Symbol;Acc:HGNC:29088]"}, {"versioned_ensembl_gene_id":"ENSG00000253355.1","gene_symbol":"AP003469.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":101128987,"end":101133486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268350.7","gene_symbol":"FAM156A","gene_name":"family with sequence similarity 156 member A [Source:HGNC Symbol;Acc:HGNC:30114]","synonyms":"TMEM29,PRO0659","biotype":"protein_coding","ncbi_id":"29057","summary":null,"start":52926402,"end":52995472,"strand":-1,"description":"family with sequence similarity 156 member A [Source:HGNC Symbol;Acc:HGNC:30114]"}, {"versioned_ensembl_gene_id":"ENSG00000248599.1","gene_symbol":"FLJ42969","gene_name":"uncharacterized LOC441374 [Source:NCBI gene;Acc:441374]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441374","summary":null,"start":101052054,"end":101076251,"strand":1,"description":"uncharacterized LOC441374 [Source:NCBI gene;Acc:441374]"}, {"versioned_ensembl_gene_id":"ENSG00000075539.14","gene_symbol":"FRYL","gene_name":"FRY like transcription coactivator [Source:HGNC Symbol;Acc:HGNC:29127]","synonyms":"MOR2,KIAA0826,DKFZp686E205,AF4p12","biotype":"protein_coding","ncbi_id":"285527","summary":null,"start":48497361,"end":48780322,"strand":-1,"description":"FRY like transcription coactivator [Source:HGNC Symbol;Acc:HGNC:29127]"}, {"versioned_ensembl_gene_id":"ENSG00000004846.16","gene_symbol":"ABCB5","gene_name":"ATP binding cassette subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:46]","synonyms":"ABCB5alpha,EST422562,ABCB5beta","biotype":"protein_coding","ncbi_id":"340273","summary":"ABCB5 belongs to the ATP-binding cassette (ABC) transporter superfamily of integral membrane proteins. These proteins participate in ATP-dependent transmembrane transport of structurally diverse molecules ranging from small ions, sugars, and peptides to more complex organic molecules (Chen et al., 2005 [PubMed 15760339]).[supplied by OMIM, Mar 2008]","start":20615207,"end":20777038,"strand":1,"description":"ATP binding cassette subfamily B member 5 [Source:HGNC Symbol;Acc:HGNC:46]"}, {"versioned_ensembl_gene_id":"ENSG00000188107.14","gene_symbol":"EYS","gene_name":"eyes shut homolog (Drosophila) [Source:HGNC Symbol;Acc:HGNC:21555]","synonyms":"dJ303F19.1,dJ1018A4.2,C6orf180,C6orf179,C6orf178,bA74E24.1,bA307F22.3,bA166P24.2,SPAM,RP25,EGFL11,EGFL10","biotype":"protein_coding","ncbi_id":"346007","summary":"The product of this gene contains multiple epidermal growth factor (EGF)-like and LamG domains. The protein is expressed in the photoreceptor layer of the retina, and the gene is mutated in autosomal recessive retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":63719980,"end":65707225,"strand":-1,"description":"eyes shut homolog (Drosophila) [Source:HGNC Symbol;Acc:HGNC:21555]"}, {"versioned_ensembl_gene_id":"ENSG00000273887.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"p58,CD158B2,cl-6,nkat2,nkat2a,nkat2b","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738479,"end":54753050,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000102241.11","gene_symbol":"HTATSF1","gene_name":"HIV-1 Tat specific factor 1 [Source:HGNC Symbol;Acc:HGNC:5276]","synonyms":"TAT-SF1","biotype":"protein_coding","ncbi_id":"27336","summary":"The protein encoded by this gene functions as a cofactor for the stimulation of transcriptional elongation by HIV-1 Tat, which binds to the HIV-1 promoter through Tat-TAR interaction. This protein may also serve as a dual-function factor to couple transcription and splicing and to facilitate their reciprocal activation. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Sep 2009]","start":136497079,"end":136512346,"strand":1,"description":"HIV-1 Tat specific factor 1 [Source:HGNC Symbol;Acc:HGNC:5276]"}, {"versioned_ensembl_gene_id":"ENSG00000243207.6","gene_symbol":"PPAN-P2RY11","gene_name":"PPAN-P2RY11 readthrough [Source:HGNC Symbol;Acc:HGNC:33526]","synonyms":null,"biotype":"protein_coding","ncbi_id":"692312","summary":"This locus represents naturally occurring read-through transcription between the adjacent PPAN and P2RY11 genes. Alternative splicing results in two transcript variants, one of which encodes a fusion protein that shares sequence identity with each individual gene product. This transcript is found to be ubiquitously expressed and is up-regulated by agents inducing granulocytic differentiation. However, its functional significance in vivo remains unclear. [provided by RefSeq, Nov 2010]","start":10106223,"end":10114780,"strand":1,"description":"PPAN-P2RY11 readthrough [Source:HGNC Symbol;Acc:HGNC:33526]"}, {"versioned_ensembl_gene_id":"ENSG00000268584.1","gene_symbol":"AC073389.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73625996,"end":73626790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162456.9","gene_symbol":"KNCN","gene_name":"kinocilin [Source:HGNC Symbol;Acc:HGNC:26488]","synonyms":"L5,KINO,FLJ32011","biotype":"protein_coding","ncbi_id":"148930","summary":null,"start":46545644,"end":46551527,"strand":-1,"description":"kinocilin [Source:HGNC Symbol;Acc:HGNC:26488]"}, {"versioned_ensembl_gene_id":"ENSG00000258481.1","gene_symbol":"AL133240.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92253493,"end":92263656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258178.1","gene_symbol":"AC016993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85958686,"end":85960946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250878.3","gene_symbol":"METTL21EP","gene_name":"methyltransferase like 21E, pseudogene [Source:HGNC Symbol;Acc:HGNC:41948]","synonyms":"METTL21CP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"121952","summary":null,"start":102880099,"end":102896033,"strand":1,"description":"methyltransferase like 21E, pseudogene [Source:HGNC Symbol;Acc:HGNC:41948]"}, {"versioned_ensembl_gene_id":"ENSG00000177463.15","gene_symbol":"NR2C2","gene_name":"nuclear receptor subfamily 2 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7972]","synonyms":"TR4,TR2R1,TAK1,hTAK1","biotype":"protein_coding","ncbi_id":"7182","summary":"This gene encodes a protein that belongs to the nuclear hormone receptor family. Members of this family act as ligand-activated transcription factors and function in many biological processes such as development, cellular differentiation and homeostasis. The activated receptor/ligand complex is translocated to the nucleus where it binds to hormone response elements of target genes. The protein encoded by this gene plays a role in protecting cells from oxidative stress and damage induced by ionizing radiation. The lack of a similar gene in mouse results in growth retardation, severe spinal curvature, subfertility, premature aging, and prostatic intraepithelial neoplasia (PIN) development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014]","start":14947584,"end":15053600,"strand":1,"description":"nuclear receptor subfamily 2 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7972]"}, {"versioned_ensembl_gene_id":"ENSG00000231247.8","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30666252,"end":30677758,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000240793.1","gene_symbol":"AC023818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48334471,"end":48334854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261538.1","gene_symbol":"AC096996.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":48164952,"end":48167238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186352.8","gene_symbol":"ANKRD37","gene_name":"ankyrin repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:29593]","synonyms":"Lrp2bp","biotype":"protein_coding","ncbi_id":"353322","summary":null,"start":185396021,"end":185400628,"strand":1,"description":"ankyrin repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:29593]"}, {"versioned_ensembl_gene_id":"ENSG00000093144.18","gene_symbol":"ECHDC1","gene_name":"ethylmalonyl-CoA decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:21489]","synonyms":"dJ351K20.2","biotype":"protein_coding","ncbi_id":"55862","summary":null,"start":127288710,"end":127343609,"strand":-1,"description":"ethylmalonyl-CoA decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:21489]"}, {"versioned_ensembl_gene_id":"ENSG00000265836.1","gene_symbol":"CCND3P2","gene_name":"cyclin D3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480307","summary":null,"start":76751305,"end":76751841,"strand":1,"description":"cyclin D3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50852]"}, {"versioned_ensembl_gene_id":"ENSG00000230413.9","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29820648,"end":29824817,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000240924.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30279091,"end":30370766,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000233241.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29898045,"end":29898411,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000204160.11","gene_symbol":"ZDHHC18","gene_name":"zinc finger DHHC-type containing 18 [Source:HGNC Symbol;Acc:HGNC:20712]","synonyms":"DKFZp667O2416","biotype":"protein_coding","ncbi_id":"84243","summary":null,"start":26826710,"end":26857602,"strand":1,"description":"zinc finger DHHC-type containing 18 [Source:HGNC Symbol;Acc:HGNC:20712]"}, {"versioned_ensembl_gene_id":"ENSG00000231928.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30283353,"end":30286914,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000232331.2","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29917929,"end":29920706,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000267597.1","gene_symbol":"RPIAP1","gene_name":"ribose 5-phosphate isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27250]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"619449","summary":null,"start":61957273,"end":61958014,"strand":-1,"description":"ribose 5-phosphate isomerase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27250]"}, {"versioned_ensembl_gene_id":"ENSG00000198171.12","gene_symbol":"DDRGK1","gene_name":"DDRGK domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16110]","synonyms":"UFBP1,dJ1187M17.3,C20orf116","biotype":"protein_coding","ncbi_id":"65992","summary":"The protein encoded by this gene interacts with components of the ubiquitin fold modifier 1 conjugation pathway and helps prevent apoptosis in ER-stressed secretory tissues. In addition, the encoded protein regulates nuclear factor-κB activity. [provided by RefSeq, Dec 2015]","start":3190350,"end":3204685,"strand":-1,"description":"DDRGK domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16110]"}, {"versioned_ensembl_gene_id":"ENSG00000270323.1","gene_symbol":"AP000860.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73640479,"end":73641037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229739.2","gene_symbol":"AL596220.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186435161,"end":186470291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277103.1","gene_symbol":"AL445670.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97151894,"end":97152694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253406.1","gene_symbol":"AC012613.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149216523,"end":149276805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100418.7","gene_symbol":"DESI1","gene_name":"desumoylating isopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:24577]","synonyms":"PPPDE2,FAM152B,D15Wsu75e","biotype":"protein_coding","ncbi_id":"27351","summary":null,"start":41598028,"end":41621096,"strand":-1,"description":"desumoylating isopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:24577]"}, {"versioned_ensembl_gene_id":"ENSG00000213612.3","gene_symbol":"FAM220CP","gene_name":"family with sequence similarity 220 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507415","summary":null,"start":97121659,"end":97122489,"strand":1,"description":"family with sequence similarity 220 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43640]"}, {"versioned_ensembl_gene_id":"ENSG00000120729.9","gene_symbol":"MYOT","gene_name":"myotilin [Source:HGNC Symbol;Acc:HGNC:12399]","synonyms":"TTID,LGMD1A,LGMD1","biotype":"protein_coding","ncbi_id":"9499","summary":"This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.[provided by RefSeq, Oct 2008]","start":137867791,"end":137887851,"strand":1,"description":"myotilin [Source:HGNC Symbol;Acc:HGNC:12399]"}, {"versioned_ensembl_gene_id":"ENSG00000228038.1","gene_symbol":"VN1R51P","gene_name":"vomeronasal 1 receptor 51 pseudogene [Source:HGNC Symbol;Acc:HGNC:37371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312801","summary":null,"start":97093694,"end":97094638,"strand":-1,"description":"vomeronasal 1 receptor 51 pseudogene [Source:HGNC Symbol;Acc:HGNC:37371]"}, {"versioned_ensembl_gene_id":"ENSG00000233044.1","gene_symbol":"AL049820.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157107727,"end":157119706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250260.1","gene_symbol":"AC113382.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138039199,"end":138039979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278325.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000228220.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"CDA12,HLA-59,D6S203,HLA-CDA12","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":29996087,"end":29999460,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000139547.7","gene_symbol":"RDH16","gene_name":"retinol dehydrogenase 16 (all-trans) [Source:HGNC Symbol;Acc:HGNC:29674]","synonyms":"SDR9C8,RODH-4","biotype":"protein_coding","ncbi_id":"8608","summary":null,"start":56951431,"end":56959374,"strand":-1,"description":"retinol dehydrogenase 16 (all-trans) [Source:HGNC Symbol;Acc:HGNC:29674]"}, {"versioned_ensembl_gene_id":"ENSG00000166435.15","gene_symbol":"XRRA1","gene_name":"X-ray radiation resistance associated 1 [Source:HGNC Symbol;Acc:HGNC:18868]","synonyms":"FLJ00225","biotype":"protein_coding","ncbi_id":"143570","summary":null,"start":74807739,"end":74949200,"strand":-1,"description":"X-ray radiation resistance associated 1 [Source:HGNC Symbol;Acc:HGNC:18868]"}, {"versioned_ensembl_gene_id":"ENSG00000206446.9","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29720576,"end":29743014,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000278879.1","gene_symbol":"AP000560.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74830574,"end":74832510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241170.2","gene_symbol":"AP001992.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":74876286,"end":74920022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232810.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31575567,"end":31578336,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000104881.15","gene_symbol":"PPP1R13L","gene_name":"protein phosphatase 1 regulatory subunit 13 like [Source:HGNC Symbol;Acc:HGNC:18838]","synonyms":"RAI,IASPP","biotype":"protein_coding","ncbi_id":"10848","summary":"IASPP is one of the most evolutionarily conserved inhibitors of p53 (TP53; MIM 191170), whereas ASPP1 (MIM 606455) and ASPP2 (MIM 602143) are activators of p53.[supplied by OMIM, Mar 2008]","start":45379634,"end":45406349,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 13 like [Source:HGNC Symbol;Acc:HGNC:18838]"}, {"versioned_ensembl_gene_id":"ENSG00000280311.1","gene_symbol":"AC131212.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132621999,"end":132622973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109775.10","gene_symbol":"UFSP2","gene_name":"UFM1 specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:25640]","synonyms":"FLJ11200,C4orf20","biotype":"protein_coding","ncbi_id":"55325","summary":"This gene encodes a highly conserved cysteine protease. The protein cleaves two C-terminal residues from ubiquitin-fold modifier 1, a ubiquitin-like post-translational modifier protein. Activation of ubiquitin-fold modifier 1 by the encoded protein exposes a C-terminal glycine residue that allows interaction with other proteins and transfer to its target protein. An allelic variant of this gene has been associated with Beukes hip dysplasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":185399540,"end":185425985,"strand":-1,"description":"UFM1 specific peptidase 2 [Source:HGNC Symbol;Acc:HGNC:25640]"}, {"versioned_ensembl_gene_id":"ENSG00000130810.19","gene_symbol":"PPAN","gene_name":"peter pan homolog (Drosophila) [Source:HGNC Symbol;Acc:HGNC:9227]","synonyms":"SSF2,SSF1,SSF,BXDC3","biotype":"protein_coding","ncbi_id":"56342","summary":"The protein encoded by this gene is an evolutionarily conserved protein similar to yeast SSF1 as well as to the gene product of the Drosophila gene peter pan (ppan). SSF1 is known to be involved in the second step of mRNA splicing. Both SSF1 and ppan are essential for cell growth and proliferation. Exogenous expression of this gene was reported to reduce the anchorage-independent growth of some tumor cells. Read-through transcription of this gene with P2RY11/P2Y(11), an adjacent downstream gene that encodes an ATP receptor, has been found. These read-through transcripts are ubiquitously present and up-regulated during granulocyte differentiation. [provided by RefSeq, Nov 2010]","start":10106289,"end":10111634,"strand":1,"description":"peter pan homolog (Drosophila) [Source:HGNC Symbol;Acc:HGNC:9227]"}, {"versioned_ensembl_gene_id":"ENSG00000225384.1","gene_symbol":"AL606662.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34717440,"end":34717992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171867.16","gene_symbol":"PRNP","gene_name":"prion protein [Source:HGNC Symbol;Acc:HGNC:9449]","synonyms":"PRP,PRIP,GSS,CJD,CD230,AltPrP","biotype":"protein_coding","ncbi_id":"5621","summary":"The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":4686236,"end":4701590,"strand":1,"description":"prion protein [Source:HGNC Symbol;Acc:HGNC:9449]"}, {"versioned_ensembl_gene_id":"ENSG00000145779.7","gene_symbol":"TNFAIP8","gene_name":"TNF alpha induced protein 8 [Source:HGNC Symbol;Acc:HGNC:17260]","synonyms":"GG2-1,SCC-S2,MDC-3.13","biotype":"protein_coding","ncbi_id":"25816","summary":null,"start":119268692,"end":119399688,"strand":1,"description":"TNF alpha induced protein 8 [Source:HGNC Symbol;Acc:HGNC:17260]"}, {"versioned_ensembl_gene_id":"ENSG00000101126.15","gene_symbol":"ADNP","gene_name":"activity dependent neuroprotector homeobox [Source:HGNC Symbol;Acc:HGNC:15766]","synonyms":"ADNP1,KIAA0784","biotype":"protein_coding","ncbi_id":"23394","summary":"Vasoactive intestinal peptide is a neuroprotective factor that has a stimulatory effect on the growth of some tumor cells and an inhibitory effect on others. This gene encodes a protein that is upregulated by vasoactive intestinal peptide and may be involved in its stimulatory effect on certain tumor cells. The encoded protein contains one homeobox and nine zinc finger domains, suggesting that it functions as a transcription factor. This gene is also upregulated in normal proliferative tissues. Finally, the encoded protein may increase the viability of certain cell types through modulation of p53 activity. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":50888919,"end":50931240,"strand":-1,"description":"activity dependent neuroprotector homeobox [Source:HGNC Symbol;Acc:HGNC:15766]"}, {"versioned_ensembl_gene_id":"ENSG00000215353.2","gene_symbol":"C1QBPP1","gene_name":"complement C1q binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1244]","synonyms":"C1QBPP","biotype":"processed_pseudogene","ncbi_id":"54098","summary":null,"start":19759359,"end":19760128,"strand":-1,"description":"complement C1q binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1244]"}, {"versioned_ensembl_gene_id":"ENSG00000273431.1","gene_symbol":"TAS2R50","gene_name":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]","synonyms":"T2R51","biotype":"protein_coding","ncbi_id":"259296","summary":"TAS2R50 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). See also TAS2R10 (MIM 604791).[supplied by OMIM, Mar 2008]","start":10985913,"end":10986912,"strand":-1,"description":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]"}, {"versioned_ensembl_gene_id":"ENSG00000262829.1","gene_symbol":"AC242308.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11115354,"end":11116274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116852.14","gene_symbol":"KIF21B","gene_name":"kinesin family member 21B [Source:HGNC Symbol;Acc:HGNC:29442]","synonyms":"KIAA0449,DKFZP434J212","biotype":"protein_coding","ncbi_id":"23046","summary":"This gene encodes a member of the kinesin superfamily. Kinesins are ATP-dependent microtubule-based motor proteins that are involved in the intracellular transport of membranous organelles. Single nucleotide polymorphisms in this gene are associated with inflammatory bowel disease and multiple sclerosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":200969390,"end":201023700,"strand":-1,"description":"kinesin family member 21B [Source:HGNC Symbol;Acc:HGNC:29442]"}, {"versioned_ensembl_gene_id":"ENSG00000259456.3","gene_symbol":"ADNP-AS1","gene_name":"ADNP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51227]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927631","summary":null,"start":50930984,"end":50945134,"strand":1,"description":"ADNP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51227]"}, {"versioned_ensembl_gene_id":"ENSG00000164199.16","gene_symbol":"ADGRV1","gene_name":"adhesion G protein-coupled receptor V1 [Source:HGNC Symbol;Acc:HGNC:17416]","synonyms":"KIAA0686,GPR98,FEB4,DKFZp761P0710,VLGR1,USH2C,MASS1","biotype":"protein_coding","ncbi_id":"84059","summary":"This gene encodes a member of the G-protein coupled receptor superfamily. The encoded protein contains a 7-transmembrane receptor domain, binds calcium and is expressed in the central nervous system. Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures. Several alternatively spliced transcripts have been described. [provided by RefSeq, Jul 2008]","start":90529344,"end":91164437,"strand":1,"description":"adhesion G protein-coupled receptor V1 [Source:HGNC Symbol;Acc:HGNC:17416]"}, {"versioned_ensembl_gene_id":"ENSG00000273286.1","gene_symbol":"BX908720.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861381,"end":28862012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147027.3","gene_symbol":"TMEM47","gene_name":"transmembrane protein 47 [Source:HGNC Symbol;Acc:HGNC:18515]","synonyms":"DKFZP761J17121,DKFZp564E153,BCMP1,VAB-9,TM4SF10","biotype":"protein_coding","ncbi_id":"83604","summary":"This gene encodes a member of the PMP22/EMP/claudin protein family. The encoded protein is localized to the ER and the plasma membrane. In dogs, transcripts of this gene exist at high levels in the brain. [provided by RefSeq, Jul 2008]","start":34627064,"end":34657288,"strand":-1,"description":"transmembrane protein 47 [Source:HGNC Symbol;Acc:HGNC:18515]"}, {"versioned_ensembl_gene_id":"ENSG00000255140.1","gene_symbol":"AC068339.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56116639,"end":56117256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158286.12","gene_symbol":"RNF207","gene_name":"ring finger protein 207 [Source:HGNC Symbol;Acc:HGNC:32947]","synonyms":"FLJ46380,FLJ32096,C1orf188","biotype":"protein_coding","ncbi_id":"388591","summary":null,"start":6205475,"end":6221299,"strand":1,"description":"ring finger protein 207 [Source:HGNC Symbol;Acc:HGNC:32947]"}, {"versioned_ensembl_gene_id":"ENSG00000231488.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"NG26,D6S82E,BAT5","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31669120,"end":31685587,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000133794.17","gene_symbol":"ARNTL","gene_name":"aryl hydrocarbon receptor nuclear translocator like [Source:HGNC Symbol;Acc:HGNC:701]","synonyms":"MOP3,JAP3,BMAL1,bHLHe5,PASD3","biotype":"protein_coding","ncbi_id":"406","summary":"The protein encoded by this gene is a basic helix-loop-helix protein that forms a heterodimer with CLOCK. This heterodimer binds E-box enhancer elements upstream of Period (PER1, PER2, PER3) and Cryptochrome (CRY1, CRY2) genes and activates transcription of these genes. PER and CRY proteins heterodimerize and repress their own transcription by interacting in a feedback loop with CLOCK/ARNTL complexes. Defects in this gene have been linked to infertility, problems with gluconeogenesis and lipogenesis, and altered sleep patterns. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":13276652,"end":13387266,"strand":1,"description":"aryl hydrocarbon receptor nuclear translocator like [Source:HGNC Symbol;Acc:HGNC:701]"}, {"versioned_ensembl_gene_id":"ENSG00000242390.1","gene_symbol":"RPL6P9","gene_name":"ribosomal protein L6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270847","summary":null,"start":142580910,"end":142582399,"strand":1,"description":"ribosomal protein L6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36484]"}, {"versioned_ensembl_gene_id":"ENSG00000254595.1","gene_symbol":"AC084337.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6488186,"end":6489377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230161.1","gene_symbol":"AL162395.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100912320,"end":100912741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274330.1","gene_symbol":"AL160191.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70230224,"end":70232426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254524.1","gene_symbol":"AC068339.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56097244,"end":56097384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135269.17","gene_symbol":"TES","gene_name":"testin LIM domain protein [Source:HGNC Symbol;Acc:HGNC:14620]","synonyms":"TESTIN,TESS-2,DKFZP586B2022","biotype":"protein_coding","ncbi_id":"26136","summary":"Cancer-associated chromosomal changes often involve regions containing fragile sites. This gene maps to a commom fragile site on chromosome 7q31.2 designated FRA7G. This gene is similar to mouse Testin, a testosterone-responsive gene encoding a Sertoli cell secretory protein containing three LIM domains. LIM domains are double zinc-finger motifs that mediate protein-protein interactions between transcription factors, cytoskeletal proteins and signaling proteins. This protein is a negative regulator of cell growth and may act as a tumor suppressor. This scaffold protein may also play a role in cell adhesion, cell spreading and in the reorganization of the actin cytoskeleton. Multiple protein isoforms are encoded by transcript variants of this gene.[provided by RefSeq, Mar 2011]","start":116210493,"end":116258783,"strand":1,"description":"testin LIM domain protein [Source:HGNC Symbol;Acc:HGNC:14620]"}, {"versioned_ensembl_gene_id":"ENSG00000265934.1","gene_symbol":"AC110743.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76703444,"end":76704254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172154.10","gene_symbol":"OR8I2","gene_name":"olfactory receptor family 8 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15310]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120586","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56093277,"end":56094286,"strand":1,"description":"olfactory receptor family 8 subfamily I member 2 [Source:HGNC Symbol;Acc:HGNC:15310]"}, {"versioned_ensembl_gene_id":"ENSG00000197261.11","gene_symbol":"C6orf141","gene_name":"chromosome 6 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:21351]","synonyms":"MGC46457","biotype":"protein_coding","ncbi_id":"135398","summary":null,"start":49550646,"end":49561907,"strand":1,"description":"chromosome 6 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:21351]"}, {"versioned_ensembl_gene_id":"ENSG00000237999.2","gene_symbol":"ACTG1P19","gene_name":"actin gamma 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51499]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644160","summary":null,"start":100731240,"end":100732355,"strand":1,"description":"actin gamma 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51499]"}, {"versioned_ensembl_gene_id":"ENSG00000249931.4","gene_symbol":"GOLGA8K","gene_name":"golgin A8 family member K [Source:HGNC Symbol;Acc:HGNC:38652]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653125","summary":null,"start":32392782,"end":32403292,"strand":-1,"description":"golgin A8 family member K [Source:HGNC Symbol;Acc:HGNC:38652]"}, {"versioned_ensembl_gene_id":"ENSG00000267035.1","gene_symbol":"AC015911.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35540039,"end":35540797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223880.1","gene_symbol":"LINC01078","gene_name":"long intergenic non-protein coding RNA 1078 [Source:HGNC Symbol;Acc:HGNC:49121]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144536","summary":null,"start":75250480,"end":75252012,"strand":1,"description":"long intergenic non-protein coding RNA 1078 [Source:HGNC Symbol;Acc:HGNC:49121]"}, {"versioned_ensembl_gene_id":"ENSG00000276974.1","gene_symbol":"AC245128.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273457.1","gene_symbol":"TAS2R13","gene_name":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]","synonyms":"TRB3,T2R13","biotype":"protein_coding","ncbi_id":"50838","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10907926,"end":10909562,"strand":-1,"description":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]"}, {"versioned_ensembl_gene_id":"ENSG00000270981.1","gene_symbol":"AC092944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157230320,"end":157231208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263028.1","gene_symbol":"TAS2R19","gene_name":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]","synonyms":"TAS2R48,TAS2R23,T2R23,T2R19","biotype":"protein_coding","ncbi_id":"259294","summary":null,"start":11021619,"end":11022620,"strand":-1,"description":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]"}, {"versioned_ensembl_gene_id":"ENSG00000243176.5","gene_symbol":"AC092944.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":157175223,"end":157381265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262525.3","gene_symbol":"TAS2R46","gene_name":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]","synonyms":"T2R54","biotype":"protein_coding","ncbi_id":"259292","summary":"TAS2R46 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Sep 2009]","start":11061365,"end":11062294,"strand":-1,"description":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]"}, {"versioned_ensembl_gene_id":"ENSG00000231620.1","gene_symbol":"AP000855.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19301613,"end":19303739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163661.3","gene_symbol":"PTX3","gene_name":"pentraxin 3 [Source:HGNC Symbol;Acc:HGNC:9692]","synonyms":"TSG-14,TNFAIP5","biotype":"protein_coding","ncbi_id":"5806","summary":"This gene encodes a member of the pentraxin protein family. The expression of this protein is induced by inflammatory cytokines in response to inflammatory stimuli in several mesenchymal and epithelial cell types, particularly endothelial cells and mononuclear phagocytes. The protein promotes fibrocyte differentiation and is involved in regulating inflammation and complement activation. It also plays a role in angiogenesis and tissue remodeling. The protein serves as a biomarker for several inflammatory conditions. [provided by RefSeq, Jun 2016]","start":157436789,"end":157443628,"strand":1,"description":"pentraxin 3 [Source:HGNC Symbol;Acc:HGNC:9692]"}, {"versioned_ensembl_gene_id":"ENSG00000262531.1","gene_symbol":"AC134349.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11198038,"end":11203301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261984.1","gene_symbol":"TAS2R14","gene_name":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]","synonyms":"TRB1,T2R14","biotype":"protein_coding","ncbi_id":"50840","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10937406,"end":11203521,"strand":-1,"description":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]"}, {"versioned_ensembl_gene_id":"ENSG00000226818.1","gene_symbol":"SLC6A6P1","gene_name":"solute carrier family 6 member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11053]","synonyms":"SLC6A6P","biotype":"processed_pseudogene","ncbi_id":"54019","summary":null,"start":19244543,"end":19246392,"strand":1,"description":"solute carrier family 6 member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11053]"}, {"versioned_ensembl_gene_id":"ENSG00000229289.1","gene_symbol":"AP000431.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19130523,"end":19134423,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226204.1","gene_symbol":"AL157359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18953264,"end":18967058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232193.1","gene_symbol":"AL157359.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18917934,"end":18935859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260642.1","gene_symbol":"AC139426.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32359538,"end":32367784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215310.2","gene_symbol":"AL050305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33410944,"end":33412173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232640.1","gene_symbol":"AL354892.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169725091,"end":169725854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279156.1","gene_symbol":"AL157359.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18917213,"end":18917429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260211.2","gene_symbol":"AC139426.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32313126,"end":32315654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154478.3","gene_symbol":"GPR26","gene_name":"G protein-coupled receptor 26 [Source:HGNC Symbol;Acc:HGNC:4481]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2849","summary":"This gene encodes a G protein-couple receptor protein. G-protein-coupled receptors are a large family of membrane proteins that are involved in cellular responses to environmental stimuli, neurotransmitters, and hormones. The encoded protein may play a role in neurodegenerative diseases. Epigenetic silencing of this gene has been observed in gliomas. [provided by RefSeq, Sep 2016]","start":123666355,"end":123694607,"strand":1,"description":"G protein-coupled receptor 26 [Source:HGNC Symbol;Acc:HGNC:4481]"}, {"versioned_ensembl_gene_id":"ENSG00000198618.5","gene_symbol":"PPIAP22","gene_name":"peptidylprolyl isomerase A pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:17236]","synonyms":"PPIAL3,PPIA3L","biotype":"processed_pseudogene","ncbi_id":"653214","summary":null,"start":18857779,"end":18858276,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:17236]"}, {"versioned_ensembl_gene_id":"ENSG00000261234.1","gene_symbol":"AC025281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65938189,"end":65938453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267074.1","gene_symbol":"AC015911.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35499690,"end":35510270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234542.1","gene_symbol":"AL357127.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123574227,"end":123583767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267349.1","gene_symbol":"AC015911.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35477994,"end":35478444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272068.1","gene_symbol":"AL365181.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156637783,"end":156641004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225152.1","gene_symbol":"AL160290.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123425713,"end":123427640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260695.1","gene_symbol":"AC022164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65861112,"end":65863784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230131.5","gene_symbol":"AL160290.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123356450,"end":123517708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118418.14","gene_symbol":"HMGN3","gene_name":"high mobility group nucleosomal binding domain 3 [Source:HGNC Symbol;Acc:HGNC:12312]","synonyms":"TRIP7","biotype":"protein_coding","ncbi_id":"9324","summary":"The protein encoded by this gene binds thyroid hormone receptor beta in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is a related pseudogene on chromosome 1. [provided by RefSeq, Jan 2016]","start":79201245,"end":79234738,"strand":-1,"description":"high mobility group nucleosomal binding domain 3 [Source:HGNC Symbol;Acc:HGNC:12312]"}, {"versioned_ensembl_gene_id":"ENSG00000255987.1","gene_symbol":"TOMM20P2","gene_name":"TOMM20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50519]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927540","summary":null,"start":35514766,"end":35515186,"strand":-1,"description":"TOMM20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50519]"}, {"versioned_ensembl_gene_id":"ENSG00000270902.1","gene_symbol":"AL160290.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123323422,"end":123323586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000000419.12","gene_symbol":"DPM1","gene_name":"dolichyl-phosphate mannosyltransferase subunit 1, catalytic [Source:HGNC Symbol;Acc:HGNC:3005]","synonyms":"MPDS,CDGIE","biotype":"protein_coding","ncbi_id":"8813","summary":"Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. Human DPM1 lacks a carboxy-terminal transmembrane domain and signal sequence and is regulated by DPM2. Mutations in this gene are associated with congenital disorder of glycosylation type Ie. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":50934867,"end":50958555,"strand":-1,"description":"dolichyl-phosphate mannosyltransferase subunit 1, catalytic [Source:HGNC Symbol;Acc:HGNC:3005]"}, {"versioned_ensembl_gene_id":"ENSG00000173210.19","gene_symbol":"ABLIM3","gene_name":"actin binding LIM protein family member 3 [Source:HGNC Symbol;Acc:HGNC:29132]","synonyms":"KIAA0843","biotype":"protein_coding","ncbi_id":"22885","summary":"This gene encodes a member of the actin-binding LIM (abLIM) family of proteins. These proteins are characterized by an N-terminal LIM domain and a C-terminal dematin-like domain. The encoded protein interacts with actin filaments and may be a component of adherens junctions in several cell types. A variant of this gene may be associated with pain sensitivity in male human patients. [provided by RefSeq, Sep 2016]","start":149141483,"end":149260542,"strand":1,"description":"actin binding LIM protein family member 3 [Source:HGNC Symbol;Acc:HGNC:29132]"}, {"versioned_ensembl_gene_id":"ENSG00000181785.2","gene_symbol":"OR5AS1","gene_name":"olfactory receptor family 5 subfamily AS member 1 [Source:HGNC Symbol;Acc:HGNC:15261]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219447","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56027654,"end":56038191,"strand":1,"description":"olfactory receptor family 5 subfamily AS member 1 [Source:HGNC Symbol;Acc:HGNC:15261]"}, {"versioned_ensembl_gene_id":"ENSG00000267312.1","gene_symbol":"AC015911.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35459481,"end":35460550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105971.14","gene_symbol":"CAV2","gene_name":"caveolin 2 [Source:HGNC Symbol;Acc:HGNC:1528]","synonyms":"CAV","biotype":"protein_coding","ncbi_id":"858","summary":"The protein encoded by this gene is a major component of the inner surface of caveolae, small invaginations of the plasma membrane, and is involved in essential cellular functions, including signal transduction, lipid metabolism, cellular growth control and apoptosis. This protein may function as a tumor suppressor. This gene and related family member (CAV1) are located next to each other on chromosome 7, and express colocalizing proteins that form a stable hetero-oligomeric complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. Additional isoforms resulting from the use of alternate in-frame translation initiation codons have also been described, and shown to have preferential localization in the cell (PMID:11238462). [provided by RefSeq, May 2011]","start":116287380,"end":116508541,"strand":1,"description":"caveolin 2 [Source:HGNC Symbol;Acc:HGNC:1528]"}, {"versioned_ensembl_gene_id":"ENSG00000142961.14","gene_symbol":"MOB3C","gene_name":"MOB kinase activator 3C [Source:HGNC Symbol;Acc:HGNC:29800]","synonyms":"MOBKL2C,MOB1E","biotype":"protein_coding","ncbi_id":"148932","summary":"The protein encoded by this gene is similar to the yeast Mob1 protein. Yeast Mob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":46607715,"end":46616891,"strand":-1,"description":"MOB kinase activator 3C [Source:HGNC Symbol;Acc:HGNC:29800]"}, {"versioned_ensembl_gene_id":"ENSG00000279086.1","gene_symbol":"AC073130.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":116209234,"end":116211511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100883.11","gene_symbol":"SRP54","gene_name":"signal recognition particle 54 [Source:HGNC Symbol;Acc:HGNC:11301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6729","summary":null,"start":34981957,"end":35029567,"strand":1,"description":"signal recognition particle 54 [Source:HGNC Symbol;Acc:HGNC:11301]"}, {"versioned_ensembl_gene_id":"ENSG00000214880.3","gene_symbol":"OR7E5P","gene_name":"olfactory receptor family 7 subfamily E member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:8435]","synonyms":"OR7F5P,OR11-12,FLJ31393","biotype":"unprocessed_pseudogene","ncbi_id":"219445","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This family member is believed to be a pseudogene. [provided by RefSeq, Jun 2009]","start":55979398,"end":55980103,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:8435]"}, {"versioned_ensembl_gene_id":"ENSG00000230456.10","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"RTK6,CD167,NEP,PTK3A,CAK,EDDR1,NTRK4","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30871677,"end":30890873,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000112110.9","gene_symbol":"MRPL18","gene_name":"mitochondrial ribosomal protein L18 [Source:HGNC Symbol;Acc:HGNC:14477]","synonyms":"HSPC071","biotype":"protein_coding","ncbi_id":"29074","summary":"This nuclear gene encodes a protein component of the larger 39S subunit of mitochondrial ribosome. This protein may also aid in the import of nuclear-encoded 5S rRNA into mitochondria. Alternative splicing results in multiple transcript variants, most of which are not predicted to encode a protein. A pseudogene of this gene is found on chromosome 16. [provided by RefSeq, Jan 2016]","start":159789812,"end":159798436,"strand":1,"description":"mitochondrial ribosomal protein L18 [Source:HGNC Symbol;Acc:HGNC:14477]"}, {"versioned_ensembl_gene_id":"ENSG00000133980.4","gene_symbol":"VRTN","gene_name":"vertebrae development associated [Source:HGNC Symbol;Acc:HGNC:20223]","synonyms":"vertnin,FLJ10811,C14orf115","biotype":"protein_coding","ncbi_id":"55237","summary":null,"start":74303069,"end":74360008,"strand":1,"description":"vertebrae development associated [Source:HGNC Symbol;Acc:HGNC:20223]"}, {"versioned_ensembl_gene_id":"ENSG00000215512.9","gene_symbol":"AP005901.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15307663,"end":15330282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248442.2","gene_symbol":"OR10J7P","gene_name":"olfactory receptor family 10 subfamily J member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:19637]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"391119","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159351093,"end":159352026,"strand":1,"description":"olfactory receptor family 10 subfamily J member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:19637]"}, {"versioned_ensembl_gene_id":"ENSG00000222465.1","gene_symbol":"RNU2-5P","gene_name":"RNA, U2 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10155]","synonyms":"u2.7,U2,RNU2P3","biotype":"snRNA","ncbi_id":"26852","summary":null,"start":70188571,"end":70188750,"strand":-1,"description":"RNA, U2 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:10155]"}, {"versioned_ensembl_gene_id":"ENSG00000102910.13","gene_symbol":"LONP2","gene_name":"lon peptidase 2, peroxisomal [Source:HGNC Symbol;Acc:HGNC:20598]","synonyms":"MGC4840,LONPL,LONP","biotype":"protein_coding","ncbi_id":"83752","summary":"In human, peroxisomes function primarily to catalyze fatty acid beta-oxidation and, as a by-product, produce hydrogen peroxide and superoxide. The protein encoded by this gene is an ATP-dependent protease that likely plays a role in maintaining overall peroxisome homeostasis as well as proteolytically degrading peroxisomal proteins damaged by oxidation. The protein has an N-terminal Lon N substrate recognition domain, an ATPase domain, a proteolytic domain, and, in some isoforms, a C-terminal peroxisome targeting sequence. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2017]","start":48244296,"end":48363122,"strand":1,"description":"lon peptidase 2, peroxisomal [Source:HGNC Symbol;Acc:HGNC:20598]"}, {"versioned_ensembl_gene_id":"ENSG00000280067.1","gene_symbol":"AC023818.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48343755,"end":48346058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270701.1","gene_symbol":"AP002802.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81842435,"end":81842669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231525.1","gene_symbol":"AC002486.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20588990,"end":20590085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226948.1","gene_symbol":"RPS4XP2","gene_name":"ribosomal protein S4X pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16563]","synonyms":"RPS4P2,RPS4L2,dJ189G13.2","biotype":"processed_pseudogene","ncbi_id":"92507","summary":null,"start":4629427,"end":4630219,"strand":-1,"description":"ribosomal protein S4X pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16563]"}, {"versioned_ensembl_gene_id":"ENSG00000258704.6","gene_symbol":"SRP54-AS1","gene_name":"SRP54 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50643]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"100506157","summary":null,"start":34920858,"end":34982532,"strand":-1,"description":"SRP54 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50643]"}, {"versioned_ensembl_gene_id":"ENSG00000276930.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736536,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000175267.14","gene_symbol":"VWA3A","gene_name":"von Willebrand factor A domain containing 3A [Source:HGNC Symbol;Acc:HGNC:27088]","synonyms":"FLJ46765,FLJ40941","biotype":"protein_coding","ncbi_id":"146177","summary":null,"start":22092538,"end":22156966,"strand":1,"description":"von Willebrand factor A domain containing 3A [Source:HGNC Symbol;Acc:HGNC:27088]"}, {"versioned_ensembl_gene_id":"ENSG00000277317.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738506,"end":54752764,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000118298.10","gene_symbol":"CA14","gene_name":"carbonic anhydrase 14 [Source:HGNC Symbol;Acc:HGNC:1372]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23632","summary":" Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA XIV is predicted to be a type I membrane protein and shares highest sequence similarity with the other transmembrane CA isoform, CA XII; however, they have different patterns of tissue-specific expression and thus may play different physiologic roles. [provided by RefSeq, Jul 2008]","start":150257159,"end":150265078,"strand":1,"description":"carbonic anhydrase 14 [Source:HGNC Symbol;Acc:HGNC:1372]"}, {"versioned_ensembl_gene_id":"ENSG00000155249.5","gene_symbol":"OR4K1","gene_name":"olfactory receptor family 4 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14726]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79544","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19930917,"end":19936757,"strand":1,"description":"olfactory receptor family 4 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14726]"}, {"versioned_ensembl_gene_id":"ENSG00000254807.1","gene_symbol":"AP003033.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55957216,"end":55957630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157510.13","gene_symbol":"AFAP1L1","gene_name":"actin filament associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:26714]","synonyms":"FLJ36748","biotype":"protein_coding","ncbi_id":"134265","summary":null,"start":149271871,"end":149341802,"strand":1,"description":"actin filament associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:26714]"}, {"versioned_ensembl_gene_id":"ENSG00000120616.15","gene_symbol":"EPC1","gene_name":"enhancer of polycomb homolog 1 [Source:HGNC Symbol;Acc:HGNC:19876]","synonyms":"Epl1","biotype":"protein_coding","ncbi_id":"80314","summary":"This gene encodes a member of the polycomb group (PcG) family. The encoded protein is a component of the NuA4 histone acetyltransferase complex and can act as both a transcriptional activator and repressor. The encoded protein has been linked to apoptosis, DNA repair, skeletal muscle differentiation, gene silencing, and adult T-cell leukemia/lymphoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":32267751,"end":32378798,"strand":-1,"description":"enhancer of polycomb homolog 1 [Source:HGNC Symbol;Acc:HGNC:19876]"}, {"versioned_ensembl_gene_id":"ENSG00000221878.12","gene_symbol":"PSG7","gene_name":"pregnancy specific beta-1-glycoprotein 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9524]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5676","summary":"This gene is a member of the pregnancy-specific glycoprotein (PSG) gene family. The PSG genes are a subgroup of the carcinoembryonic antigen (CEA) family of immunoglobulin-like genes, and are found in a gene cluster at 19q13.1-q13.2 telomeric to another cluster of CEA-related genes. The PSG genes are expressed by placental trophoblasts and released into the maternal circulation during pregnancy, and are thought to be essential for maintenance of normal pregnancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":42924132,"end":42937178,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:9524]"}, {"versioned_ensembl_gene_id":"ENSG00000196266.4","gene_symbol":"OR10J3","gene_name":"olfactory receptor family 10 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14992]","synonyms":"OR10J3P","biotype":"protein_coding","ncbi_id":"441911","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This gene is considered a pseudogene because the encoded protein is truncated and missing the last transmembrane domain in several mammals.[provided by RefSeq, Jun 2021]","start":159313670,"end":159314659,"strand":-1,"description":"olfactory receptor family 10 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:14992]"}, {"versioned_ensembl_gene_id":"ENSG00000224539.1","gene_symbol":"SAGE4P","gene_name":"sarcoma antigen 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:51339]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442465","summary":null,"start":135598927,"end":135615431,"strand":1,"description":"sarcoma antigen 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:51339]"}, {"versioned_ensembl_gene_id":"ENSG00000227349.1","gene_symbol":"CEACAMP7","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:1829]","synonyms":"CGM14","biotype":"unprocessed_pseudogene","ncbi_id":"1095","summary":null,"start":42949503,"end":42950387,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:1829]"}, {"versioned_ensembl_gene_id":"ENSG00000280058.1","gene_symbol":"AL117378.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131910191,"end":131911527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255416.1","gene_symbol":"AP003033.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55948120,"end":55948924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136636.12","gene_symbol":"KCTD3","gene_name":"potassium channel tetramerization domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21305]","synonyms":"NY-REN-45","biotype":"protein_coding","ncbi_id":"51133","summary":"This gene encodes a member of the potassium channel tetramerization-domain containing (KCTD) protein family. Members of this protein family regulate the biophysical characteristics of ion channels. In mouse, this protein interacts with hyperpolarization-activated cyclic nucleotide-gated channel complex 3 and enhances its cell surface expression and current density. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":215567392,"end":215621807,"strand":1,"description":"potassium channel tetramerization domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21305]"}, {"versioned_ensembl_gene_id":"ENSG00000282881.1","gene_symbol":"AL136373.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46532166,"end":46533614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187612.1","gene_symbol":"OR5W2","gene_name":"olfactory receptor family 5 subfamily W member 2 [Source:HGNC Symbol;Acc:HGNC:15299]","synonyms":"OR5W3P,OR5W2P","biotype":"protein_coding","ncbi_id":"390148","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55913650,"end":55914582,"strand":-1,"description":"olfactory receptor family 5 subfamily W member 2 [Source:HGNC Symbol;Acc:HGNC:15299]"}, {"versioned_ensembl_gene_id":"ENSG00000228708.1","gene_symbol":"AL109763.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":18477358,"end":18486599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198604.10","gene_symbol":"BAZ1A","gene_name":"bromodomain adjacent to zinc finger domain 1A [Source:HGNC Symbol;Acc:HGNC:960]","synonyms":"WCRF180,WALp1,hACF1,ACF1","biotype":"protein_coding","ncbi_id":"11177","summary":"The BAZ1A gene encodes the accessory subunit of the ATP-dependent chromatin assembly factor (ACF), a member of the ISWI ('imitation switch') family of chromatin remodeling complexes (summarized by Racki et al., 2009 [PubMed 20033039]).[supplied by OMIM, Apr 2010]","start":34752731,"end":34875647,"strand":-1,"description":"bromodomain adjacent to zinc finger domain 1A [Source:HGNC Symbol;Acc:HGNC:960]"}, {"versioned_ensembl_gene_id":"ENSG00000159648.11","gene_symbol":"TEPP","gene_name":"testis, prostate and placenta expressed [Source:HGNC Symbol;Acc:HGNC:33745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"374739","summary":null,"start":57976435,"end":57988116,"strand":1,"description":"testis, prostate and placenta expressed [Source:HGNC Symbol;Acc:HGNC:33745]"}, {"versioned_ensembl_gene_id":"ENSG00000198707.14","gene_symbol":"CEP290","gene_name":"centrosomal protein 290 [Source:HGNC Symbol;Acc:HGNC:29021]","synonyms":"BBS14,3H11Ag,SLSN6,rd16,POC3,NPHP6,MKS4,LCA10,KIAA0373,JBTS5,FLJ13615,CT87","biotype":"protein_coding","ncbi_id":"80184","summary":"This gene encodes a protein with 13 putative coiled-coil domains, a region with homology to SMC chromosome segregation ATPases, six KID motifs, three tropomyosin homology domains and an ATP/GTP binding site motif A. The protein is localized to the centrosome and cilia and has sites for N-glycosylation, tyrosine sulfation, phosphorylation, N-myristoylation, and amidation. Mutations in this gene have been associated with Joubert syndrome and nephronophthisis and the presence of antibodies against this protein is associated with several forms of cancer. [provided by RefSeq, Jul 2008]","start":88049014,"end":88142216,"strand":-1,"description":"centrosomal protein 290 [Source:HGNC Symbol;Acc:HGNC:29021]"}, {"versioned_ensembl_gene_id":"ENSG00000279168.2","gene_symbol":"AC105052.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":102579104,"end":102679295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229094.9","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"MGC22487,Oct4,OCT3,OTF3","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31158060,"end":31164434,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000270249.1","gene_symbol":"AC093668.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":102541501,"end":102592444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272949.1","gene_symbol":"AC093668.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":102483344,"end":102543764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129968.15","gene_symbol":"ABHD17A","gene_name":"abhydrolase domain containing 17A [Source:HGNC Symbol;Acc:HGNC:28756]","synonyms":"FAM108A1,C19orf27,MGC5244","biotype":"protein_coding","ncbi_id":"81926","summary":null,"start":1876810,"end":1885547,"strand":-1,"description":"abhydrolase domain containing 17A [Source:HGNC Symbol;Acc:HGNC:28756]"}, {"versioned_ensembl_gene_id":"ENSG00000165934.12","gene_symbol":"CPSF2","gene_name":"cleavage and polyadenylation specific factor 2 [Source:HGNC Symbol;Acc:HGNC:2325]","synonyms":"KIAA1367,CPSF100","biotype":"protein_coding","ncbi_id":"53981","summary":null,"start":92121937,"end":92172145,"strand":1,"description":"cleavage and polyadenylation specific factor 2 [Source:HGNC Symbol;Acc:HGNC:2325]"}, {"versioned_ensembl_gene_id":"ENSG00000228049.7","gene_symbol":"POLR2J2","gene_name":"RNA polymerase II subunit J2 [Source:HGNC Symbol;Acc:HGNC:23208]","synonyms":"RPB11b1,RPB11b1,HRPB11B","biotype":"protein_coding","ncbi_id":"246721","summary":"This gene is a member of the RNA polymerase II subunit 11 gene family, which includes three genes in a cluster on chromosome 7q22.1 and a pseudogene on chromosome 7p13. The founding member of this family, DNA directed RNA polymerase II polypeptide J, has been shown to encode a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This locus produces multiple, alternatively spliced transcripts that potentially express isoforms with distinct C-termini compared to DNA directed RNA polymerase II polypeptide J. Most or all variants are spliced to include additional non-coding exons at the 3' end which makes them candidates for nonsense-mediated decay (NMD). Consequently, it is not known if this locus expresses a protein or proteins in vivo. [provided by RefSeq, Jul 2008]","start":102665368,"end":102671629,"strand":-1,"description":"RNA polymerase II subunit J2 [Source:HGNC Symbol;Acc:HGNC:23208]"}, {"versioned_ensembl_gene_id":"ENSG00000065361.14","gene_symbol":"ERBB3","gene_name":"erb-b2 receptor tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:3431]","synonyms":"LCCS2,HER3","biotype":"protein_coding","ncbi_id":"2065","summary":"This gene encodes a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases. This membrane-bound protein has a neuregulin binding domain but not an active kinase domain. It therefore can bind this ligand but not convey the signal into the cell through protein phosphorylation. However, it does form heterodimers with other EGF receptor family members which do have kinase activity. Heterodimerization leads to the activation of pathways which lead to cell proliferation or differentiation. Amplification of this gene and/or overexpression of its protein have been reported in numerous cancers, including prostate, bladder, and breast tumors. Alternate transcriptional splice variants encoding different isoforms have been characterized. One isoform lacks the intermembrane region and is secreted outside the cell. This form acts to modulate the activity of the membrane-bound form. Additional splice variants have also been reported, but they have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":56079857,"end":56103505,"strand":1,"description":"erb-b2 receptor tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:3431]"}, {"versioned_ensembl_gene_id":"ENSG00000267645.5","gene_symbol":"POLR2J2","gene_name":"RNA polymerase II subunit J2 [Source:NCBI gene;Acc:246721]","synonyms":"RPB11b1,RPB11b1,HRPB11B","biotype":"protein_coding","ncbi_id":"246721","summary":"This gene is a member of the RNA polymerase II subunit 11 gene family, which includes three genes in a cluster on chromosome 7q22.1 and a pseudogene on chromosome 7p13. The founding member of this family, DNA directed RNA polymerase II polypeptide J, has been shown to encode a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This locus produces multiple, alternatively spliced transcripts that potentially express isoforms with distinct C-termini compared to DNA directed RNA polymerase II polypeptide J. Most or all variants are spliced to include additional non-coding exons at the 3' end which makes them candidates for nonsense-mediated decay (NMD). Consequently, it is not known if this locus expresses a protein or proteins in vivo. [provided by RefSeq, Jul 2008]","start":102637049,"end":102671641,"strand":-1,"description":"RNA polymerase II subunit J2 [Source:NCBI gene;Acc:246721]"}, {"versioned_ensembl_gene_id":"ENSG00000125695.12","gene_symbol":"AC046185.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63702845,"end":63752097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205238.9","gene_symbol":"SPDYE2","gene_name":"speedy/RINGO cell cycle regulator family member E2 [Source:HGNC Symbol;Acc:HGNC:33841]","synonyms":"MGC119295","biotype":"protein_coding","ncbi_id":"441273","summary":null,"start":102551232,"end":102562308,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E2 [Source:HGNC Symbol;Acc:HGNC:33841]"}, {"versioned_ensembl_gene_id":"ENSG00000279369.1","gene_symbol":"AC046185.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":63700847,"end":63702670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126821.7","gene_symbol":"SGPP1","gene_name":"sphingosine-1-phosphate phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:17720]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81537","summary":"Sphingosine-1-phosphate (S1P) is a bioactive sphingolipid metabolite that regulates diverse biologic processes. SGPP1 catalyzes the degradation of S1P via salvage and recycling of sphingosine into long-chain ceramides (Mandala et al., 2000 [PubMed 10859351]; Le Stunff et al., 2007 [PubMed 17895250]).[supplied by OMIM, Jun 2009]","start":63684214,"end":63728039,"strand":-1,"description":"sphingosine-1-phosphate phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:17720]"}, {"versioned_ensembl_gene_id":"ENSG00000138030.12","gene_symbol":"KHK","gene_name":"ketohexokinase [Source:HGNC Symbol;Acc:HGNC:6315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3795","summary":"This gene encodes ketohexokinase that catalyzes conversion of fructose to fructose-1-phosphate. The product of this gene is the first enzyme with a specialized pathway that catabolizes dietary fructose. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":27086747,"end":27100772,"strand":1,"description":"ketohexokinase [Source:HGNC Symbol;Acc:HGNC:6315]"}, {"versioned_ensembl_gene_id":"ENSG00000258766.1","gene_symbol":"DIO2-AS1","gene_name":"DIO2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44153]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100628307","summary":null,"start":80211419,"end":80455469,"strand":1,"description":"DIO2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44153]"}, {"versioned_ensembl_gene_id":"ENSG00000258778.2","gene_symbol":"AL161670.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63734697,"end":63735923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211448.11","gene_symbol":"DIO2","gene_name":"iodothyronine deiodinase 2 [Source:HGNC Symbol;Acc:HGNC:2884]","synonyms":"TXDI2,SelY","biotype":"protein_coding","ncbi_id":"1734","summary":"The protein encoded by this gene belongs to the iodothyronine deiodinase family. It catalyzes the conversion of prohormone thyroxine (3,5,3',5'-tetraiodothyronine, T4) to the bioactive thyroid hormone (3,5,3'-triiodothyronine, T3) by outer ring 5'-deiodination. This gene is widely expressed, including in thyroid and brain. It is thought to be responsible for the 'local' production of T3, and thus important in influencing thyroid hormone action in these tissues. It has also been reported to be highly expressed in thyroids of patients with Graves disease, and in follicular adenomas. The intrathyroidal T4 to T3 conversion by this enzyme may contribute significantly to the relative increase in thyroidal T3 production in these patients. This protein is a selenoprotein containing the non-standard amino acid, selenocysteine (Sec), which is encoded by the UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Unlike the other two members (DIO1 and DIO3) of this enzyme family, the mRNA for this gene contains an additional in-frame UGA codon that has been reported (in human) to function either as a Sec or a stop codon, which can result in two isoforms with one or two Sec residues; however, only the upstream Sec (conserved with the single Sec residue found at the active site in DIO1 and DIO3) was shown to be essential for enzyme activity (PMID:10403186). Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2018]","start":80197527,"end":80387757,"strand":-1,"description":"iodothyronine deiodinase 2 [Source:HGNC Symbol;Acc:HGNC:2884]"}, {"versioned_ensembl_gene_id":"ENSG00000132286.11","gene_symbol":"TIMM10B","gene_name":"translocase of inner mitochondrial membrane 10B [Source:HGNC Symbol;Acc:HGNC:4022]","synonyms":"Tim9b,TIM10B,FXC1","biotype":"protein_coding","ncbi_id":"26515","summary":"FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004]","start":6481447,"end":6484679,"strand":1,"description":"translocase of inner mitochondrial membrane 10B [Source:HGNC Symbol;Acc:HGNC:4022]"}, {"versioned_ensembl_gene_id":"ENSG00000267368.1","gene_symbol":"UPK3BL1","gene_name":"uroplakin 3B like 1 [Source:HGNC Symbol;Acc:HGNC:37278]","synonyms":"UPK3BL,UPLP","biotype":"protein_coding","ncbi_id":"100134938","summary":null,"start":102637025,"end":102642791,"strand":-1,"description":"uroplakin 3B like 1 [Source:HGNC Symbol;Acc:HGNC:37278]"}, {"versioned_ensembl_gene_id":"ENSG00000266173.6","gene_symbol":"STRADA","gene_name":"STE20-related kinase adaptor alpha [Source:HGNC Symbol;Acc:HGNC:30172]","synonyms":"STRAD,Stlk,NY-BR-96,LYK5","biotype":"protein_coding","ncbi_id":"92335","summary":"The protein encoded by this gene contains a STE20-like kinase domain, but lacks several residues that are critical for catalytic activity, so it is termed a 'pseudokinase'. The protein forms a heterotrimeric complex with serine/threonine kinase 11 (STK11, also known as LKB1) and the scaffolding protein calcium binding protein 39 (CAB39, also known as MO25). The protein activates STK11 leading to the phosphorylation of both proteins and excluding STK11 from the nucleus. The protein is necessary for STK11-induced G1 cell cycle arrest. A mutation in this gene has been shown to result in polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described but their full-length nature is not known. [provided by RefSeq, Sep 2009]","start":63682336,"end":63741986,"strand":-1,"description":"STE20-related kinase adaptor alpha [Source:HGNC Symbol;Acc:HGNC:30172]"}, {"versioned_ensembl_gene_id":"ENSG00000218617.1","gene_symbol":"AL121949.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63392222,"end":63392606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258411.2","gene_symbol":"AL161670.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63762013,"end":63762149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218274.2","gene_symbol":"AL121949.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63395007,"end":63397106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270912.1","gene_symbol":"RPS28P1","gene_name":"ribosomal protein S28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652980","summary":null,"start":63808546,"end":63808732,"strand":1,"description":"ribosomal protein S28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23561]"}, {"versioned_ensembl_gene_id":"ENSG00000218048.2","gene_symbol":"AL121949.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63440766,"end":63443580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168255.19","gene_symbol":"POLR2J3","gene_name":"RNA polymerase II subunit J3 [Source:HGNC Symbol;Acc:HGNC:33853]","synonyms":null,"biotype":"protein_coding","ncbi_id":"548644","summary":"This gene is a member of the RNA polymerase II subunit 11 gene family, which includes three genes in a cluster on chromosome 7q22.1 and a pseudogene on chromosome 7p13. The founding member of this family, DNA directed RNA polymerase II polypeptide J, has been shown to encode a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This locus produces multiple, alternatively spliced transcripts that potentially express isoforms with distinct C-termini compared to DNA directed RNA polymerase II polypeptide J. Most or all variants are spliced to include additional non-coding exons at the 3' end which makes them candidates for nonsense-mediated decay (NMD). Consequently, it is not known if this locus expresses a protein or proteins in vivo. [provided by RefSeq, Jul 2008]","start":102537918,"end":102572656,"strand":-1,"description":"RNA polymerase II subunit J3 [Source:HGNC Symbol;Acc:HGNC:33853]"}, {"versioned_ensembl_gene_id":"ENSG00000104524.13","gene_symbol":"PYCR3","gene_name":"pyrroline-5-carboxylate reductase 3 [Source:HGNC Symbol;Acc:HGNC:25846]","synonyms":"PYCRL,FLJ13852","biotype":"protein_coding","ncbi_id":"65263","summary":"This gene encodes a protein that belongs to the pyrroline-5-carboxylate reductase family of enzymes. Members of this family catalyze the final step in proline biosynthesis, converting pyrroline-5-carboxylate to proline. Glutamate and ornithine are precursors in the synthesis of proline. The protein encoded by this gene is a cytoplasmic enzyme involved in the biosynthesis of proline from ornithine. [provided by RefSeq, Aug 2016]","start":143603913,"end":143609773,"strand":-1,"description":"pyrroline-5-carboxylate reductase 3 [Source:HGNC Symbol;Acc:HGNC:25846]"}, {"versioned_ensembl_gene_id":"ENSG00000225121.2","gene_symbol":"EEF1B2P5","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32476]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442227","summary":null,"start":63480134,"end":63481876,"strand":1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32476]"}, {"versioned_ensembl_gene_id":"ENSG00000198722.14","gene_symbol":"UNC13B","gene_name":"unc-13 homolog B [Source:HGNC Symbol;Acc:HGNC:12566]","synonyms":"UNC13,hmunc13,Unc13h2","biotype":"protein_coding","ncbi_id":"10497","summary":"This gene is expressed in the kidney cortical epithelial cells and is upregulated by hyperglycemia. The encoded protein shares a high level of similarity to the rat homolog, and contains 3 C2 domains and a diacylglycerol-binding C1 domain. Hyperglycemia increases the levels of diacylglycerol, which has been shown to induce apoptosis in cells transfected with this gene and thus contribute to the renal cell complications of hyperglycemia. Studies in other species also indicate a role for this protein in the priming step of synaptic vesicle exocytosis. [provided by RefSeq, Jul 2008]","start":35161992,"end":35405338,"strand":1,"description":"unc-13 homolog B [Source:HGNC Symbol;Acc:HGNC:12566]"}, {"versioned_ensembl_gene_id":"ENSG00000227606.2","gene_symbol":"AC005392.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43153279,"end":43160862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230529.1","gene_symbol":"CEACAMP9","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:1831]","synonyms":"CGM16","biotype":"unprocessed_pseudogene","ncbi_id":"1097","summary":null,"start":43096456,"end":43097360,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:1831]"}, {"versioned_ensembl_gene_id":"ENSG00000170848.15","gene_symbol":"PSG6","gene_name":"pregnancy specific beta-1-glycoprotein 6 [Source:HGNC Symbol;Acc:HGNC:9523]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5675","summary":"This gene is a member of the pregnancy-specific glycoprotein (PSG) gene family. The PSG genes are a subgroup of the carcinoembryonic antigen (CEA) family of immunoglobulin-like genes, and are found in a gene cluster at 19q13.1-q13.2 telomeric to another cluster of CEA-related genes. The PSG genes are expressed by placental trophoblasts and released into the maternal circulation during pregnancy, and are thought to be essential for maintenance of normal pregnancy. The protein encoded by this gene contains the Arg-Gly-Asp tripeptide associated with cellular adhesion and recognition. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":42902079,"end":42919563,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 6 [Source:HGNC Symbol;Acc:HGNC:9523]"}, {"versioned_ensembl_gene_id":"ENSG00000165457.13","gene_symbol":"FOLR2","gene_name":"folate receptor beta [Source:HGNC Symbol;Acc:HGNC:3793]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2350","summary":"The protein encoded by this gene is a member of the folate receptor (FOLR) family, and these genes exist in a cluster on chromosome 11. Members of this gene family have a high affinity for folic acid and for several reduced folic acid derivatives, and they mediate delivery of 5-methyltetrahydrofolate to the interior of cells. This protein has a 68% and 79% sequence homology with the FOLR1 and FOLR3 proteins, respectively. Although this protein was originally thought to be specific to placenta, it can also exist in other tissues, and it may play a role in the transport of methotrexate in synovial macrophages in rheumatoid arthritis patients. Multiple transcript variants that encode the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":72216601,"end":72221950,"strand":1,"description":"folate receptor beta [Source:HGNC Symbol;Acc:HGNC:3793]"}, {"versioned_ensembl_gene_id":"ENSG00000233190.1","gene_symbol":"RPS24P13","gene_name":"ribosomal protein S24 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216338","summary":null,"start":32231849,"end":32232245,"strand":-1,"description":"ribosomal protein S24 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36805]"}, {"versioned_ensembl_gene_id":"ENSG00000196505.10","gene_symbol":"GDAP2","gene_name":"ganglioside induced differentiation associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18010]","synonyms":"dJ776P7.1,MACROD3,FLJ20142","biotype":"protein_coding","ncbi_id":"54834","summary":null,"start":117863485,"end":117929630,"strand":-1,"description":"ganglioside induced differentiation associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18010]"}, {"versioned_ensembl_gene_id":"ENSG00000215846.6","gene_symbol":"MPTX1","gene_name":"mucosal pentraxin 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:48364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649458","summary":null,"start":159276503,"end":159277111,"strand":1,"description":"mucosal pentraxin 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:48364]"}, {"versioned_ensembl_gene_id":"ENSG00000250426.2","gene_symbol":"FTLP10","gene_name":"ferritin light chain pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37959]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100130017","summary":null,"start":68182292,"end":68212470,"strand":1,"description":"ferritin light chain pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37959]"}, {"versioned_ensembl_gene_id":"ENSG00000248642.1","gene_symbol":"OR10J2P","gene_name":"olfactory receptor family 10 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14991]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391117","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159279041,"end":159280001,"strand":-1,"description":"olfactory receptor family 10 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14991]"}, {"versioned_ensembl_gene_id":"ENSG00000103005.11","gene_symbol":"USB1","gene_name":"U6 snRNA biogenesis phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:25792]","synonyms":"Mpn1,HVSL1,FLJ13154,C16orf57","biotype":"protein_coding","ncbi_id":"79650","summary":"This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2011]","start":57999546,"end":58021618,"strand":1,"description":"U6 snRNA biogenesis phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:25792]"}, {"versioned_ensembl_gene_id":"ENSG00000177733.6","gene_symbol":"HNRNPA0","gene_name":"heterogeneous nuclear ribonucleoprotein A0 [Source:HGNC Symbol;Acc:HGNC:5030]","synonyms":"HNRPA0,hnRNPA0","biotype":"protein_coding","ncbi_id":"10949","summary":"This gene belongs to the A/B subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two repeats of quasi-RRM domains that bind RNAs, followed by a glycine-rich C-terminus. [provided by RefSeq, Jul 2008]","start":137745651,"end":137754376,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A0 [Source:HGNC Symbol;Acc:HGNC:5030]"}, {"versioned_ensembl_gene_id":"ENSG00000236377.1","gene_symbol":"AC084809.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32905662,"end":32906584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227360.1","gene_symbol":"AL512658.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156493226,"end":156499771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124900.12","gene_symbol":"TRIM51","gene_name":"tripartite motif-containing 51 [Source:HGNC Symbol;Acc:HGNC:19023]","synonyms":"TRIM51A,SPRYD5","biotype":"protein_coding","ncbi_id":"84767","summary":null,"start":55883297,"end":55891810,"strand":1,"description":"tripartite motif-containing 51 [Source:HGNC Symbol;Acc:HGNC:19023]"}, {"versioned_ensembl_gene_id":"ENSG00000197214.5","gene_symbol":"TCEA1P1","gene_name":"transcription elongation factor A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11613]","synonyms":"TCEA1P,GTF2SP","biotype":"processed_pseudogene","ncbi_id":"6918","summary":null,"start":97067749,"end":97068628,"strand":1,"description":"transcription elongation factor A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11613]"}, {"versioned_ensembl_gene_id":"ENSG00000124243.17","gene_symbol":"BCAS4","gene_name":"breast carcinoma amplified sequence 4 [Source:HGNC Symbol;Acc:HGNC:14367]","synonyms":"FLJ20495,CNOL","biotype":"protein_coding","ncbi_id":"55653","summary":null,"start":50794894,"end":50882676,"strand":1,"description":"breast carcinoma amplified sequence 4 [Source:HGNC Symbol;Acc:HGNC:14367]"}, {"versioned_ensembl_gene_id":"ENSG00000270697.1","gene_symbol":"AC106791.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137761546,"end":137761936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279353.1","gene_symbol":"AP001324.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74698231,"end":74699658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220347.1","gene_symbol":"AL355297.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156662050,"end":156662437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000054938.15","gene_symbol":"CHRDL2","gene_name":"chordin like 2 [Source:HGNC Symbol;Acc:HGNC:24168]","synonyms":"BNF1","biotype":"protein_coding","ncbi_id":"25884","summary":"This gene encodes a member of the chordin family of proteins. Chordin family members are secreted proteins that share a cysteine-rich pro-collagen repeat domain and associate with members of the transforming growth factor beta superfamily. In vitro assays demonstrate a direct interaction between the encoded protein and human activin A. This gene is expressed in many tissues including osteoblasts, where it is differentially expressed during differentiation. In addition, its expression is upregulated in human osteoarthritic joint cartilage, suggesting a role in adult cartilage regeneration. [provided by RefSeq, Jan 2015]","start":74696429,"end":74731385,"strand":-1,"description":"chordin like 2 [Source:HGNC Symbol;Acc:HGNC:24168]"}, {"versioned_ensembl_gene_id":"ENSG00000226306.6","gene_symbol":"NPY6R","gene_name":"neuropeptide Y receptor Y6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7959]","synonyms":"NPY1RL,PP2,NPY6RP","biotype":"transcribed_processed_pseudogene","ncbi_id":"4888","summary":null,"start":137801193,"end":137810751,"strand":1,"description":"neuropeptide Y receptor Y6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7959]"}, {"versioned_ensembl_gene_id":"ENSG00000271265.1","gene_symbol":"AL355297.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156774217,"end":156774662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242793.1","gene_symbol":"AC135999.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26851132,"end":26851610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228376.3","gene_symbol":"GAS2L1P2","gene_name":"growth arrest specific 2 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27986]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"340508","summary":null,"start":97075671,"end":97081945,"strand":-1,"description":"growth arrest specific 2 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27986]"}, {"versioned_ensembl_gene_id":"ENSG00000235518.2","gene_symbol":"AC011196.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26657030,"end":26658763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266975.1","gene_symbol":"FARSA-AS1","gene_name":"FARSA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50479]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106144598","summary":null,"start":12930522,"end":12933296,"strand":1,"description":"FARSA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50479]"}, {"versioned_ensembl_gene_id":"ENSG00000284715.1","gene_symbol":"AP001153.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":104975356,"end":104976116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278840.1","gene_symbol":"AC009878.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26557598,"end":26557937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179115.10","gene_symbol":"FARSA","gene_name":"phenylalanyl-tRNA synthetase alpha subunit [Source:HGNC Symbol;Acc:HGNC:3592]","synonyms":"FARSLA,FARSL,CML33","biotype":"protein_coding","ncbi_id":"2193","summary":"Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. This gene encodes a product which is similar to the catalytic subunit of prokaryotic and Saccharomyces cerevisiae phenylalanyl-tRNA synthetases (PheRS). This gene product has been shown to be expressed in a tumor-selective and cell cycle stage- and differentiation-dependent manner, the first member of the tRNA synthetase gene family shown to exhibit this type of regulated expression [provided by RefSeq, Jul 2008]","start":12922479,"end":12934037,"strand":-1,"description":"phenylalanyl-tRNA synthetase alpha subunit [Source:HGNC Symbol;Acc:HGNC:3592]"}, {"versioned_ensembl_gene_id":"ENSG00000226842.1","gene_symbol":"AL158834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32281686,"end":32282829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229327.1","gene_symbol":"AL391839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32347397,"end":32374488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166206.14","gene_symbol":"GABRB3","gene_name":"gamma-aminobutyric acid type A receptor beta3 subunit [Source:HGNC Symbol;Acc:HGNC:4083]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2562","summary":"This gene encodes a member of the ligand-gated ionic channel family. The encoded protein is one the subunits of a multi-subunit chloride channel that serves as the receptor for gamma-aminobutyric acid, a major inhibitory neurotransmitter of the mammalian nervous system. This gene is located on the long arm of chromosome 15 in a cluster with two other genes encoding related subunits of the family. This gene may be associated with the pathogenesis of several disorders including Angelman syndrome, Prader-Willi syndrome, nonsyndromic orofacial clefts, epilepsy and autism. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013]","start":26543546,"end":26939539,"strand":-1,"description":"gamma-aminobutyric acid type A receptor beta3 subunit [Source:HGNC Symbol;Acc:HGNC:4083]"}, {"versioned_ensembl_gene_id":"ENSG00000242221.8","gene_symbol":"PSG2","gene_name":"pregnancy specific beta-1-glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:9519]","synonyms":"PSGGB,PSG1,PSBG2,CEA","biotype":"protein_coding","ncbi_id":"5670","summary":"The human pregnancy-specific glycoproteins (PSGs) are a family of proteins that are synthesized in large amounts by placental trophoblasts and released into the maternal circulation during pregnancy. Molecular cloning and analysis of several PSG genes has indicated that the PSGs form a subgroup of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily of genes. Members of the CEA family consist of a single N domain, with structural similarity to the immunoglobulin variable domains, followed by a variable number of immunoglobulin constant-like A and/or B domains. Most PSGs have an arg-gly-asp (RGD) motif, which has been shown to function as an adhesion recognition signal for several integrins, in the N-terminal domain (summary by Teglund et al., 1994 [PubMed 7851896]). For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":43064211,"end":43083045,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:9519]"}, {"versioned_ensembl_gene_id":"ENSG00000250072.5","gene_symbol":"AC091940.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149063317,"end":149109787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179639.10","gene_symbol":"FCER1A","gene_name":"Fc fragment of IgE receptor Ia [Source:HGNC Symbol;Acc:HGNC:3609]","synonyms":"FCE1A","biotype":"protein_coding","ncbi_id":"2205","summary":"The immunoglobulin epsilon receptor (IgE receptor) is the initiator of the allergic response. When two or more high-affinity IgE receptors are brought together by allergen-bound IgE molecules, mediators such as histamine that are responsible for allergy symptoms are released. This receptor is comprised of an alpha subunit, a beta subunit, and two gamma subunits. The protein encoded by this gene represents the alpha subunit. [provided by RefSeq, Aug 2011]","start":159289714,"end":159308224,"strand":1,"description":"Fc fragment of IgE receptor Ia [Source:HGNC Symbol;Acc:HGNC:3609]"}, {"versioned_ensembl_gene_id":"ENSG00000204941.13","gene_symbol":"PSG5","gene_name":"pregnancy specific beta-1-glycoprotein 5 [Source:HGNC Symbol;Acc:HGNC:9522]","synonyms":"PSG,FL-NCA-3","biotype":"protein_coding","ncbi_id":"5673","summary":"The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":43166256,"end":43186536,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 5 [Source:HGNC Symbol;Acc:HGNC:9522]"}, {"versioned_ensembl_gene_id":"ENSG00000267765.1","gene_symbol":"AC100793.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42683187,"end":42699466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108797.11","gene_symbol":"CNTNAP1","gene_name":"contactin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:8011]","synonyms":"p190,NRXN4,CNTNAP,Caspr","biotype":"protein_coding","ncbi_id":"8506","summary":"The gene product was initially identified as a 190-kD protein associated with the contactin-PTPRZ1 complex. The 1,384-amino acid protein, also designated p190 or CASPR for 'contactin-associated protein,' includes an extracellular domain with several putative protein-protein interaction domains, a putative transmembrane domain, and a 74-amino acid cytoplasmic domain. Northern blot analysis showed that the gene is transcribed predominantly in brain as a transcript of 6.2 kb, with weak expression in several other tissues tested. The architecture of its extracellular domain is similar to that of neurexins, and this protein may be the signaling subunit of contactin, enabling recruitment and activation of intracellular signaling pathways in neurons. [provided by RefSeq, Jan 2009]","start":42682613,"end":42699814,"strand":1,"description":"contactin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:8011]"}, {"versioned_ensembl_gene_id":"ENSG00000105374.9","gene_symbol":"NKG7","gene_name":"natural killer cell granule protein 7 [Source:HGNC Symbol;Acc:HGNC:7830]","synonyms":"GMP-17,GIG1","biotype":"protein_coding","ncbi_id":"4818","summary":null,"start":51371606,"end":51372715,"strand":-1,"description":"natural killer cell granule protein 7 [Source:HGNC Symbol;Acc:HGNC:7830]"}, {"versioned_ensembl_gene_id":"ENSG00000233204.1","gene_symbol":"MAPRE1P3","gene_name":"MAPRE1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422229","summary":null,"start":165285253,"end":165286048,"strand":1,"description":"MAPRE1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37762]"}, {"versioned_ensembl_gene_id":"ENSG00000169507.9","gene_symbol":"SLC38A11","gene_name":"solute carrier family 38 member 11 [Source:HGNC Symbol;Acc:HGNC:26836]","synonyms":"FLJ39822,AVT2","biotype":"protein_coding","ncbi_id":"151258","summary":null,"start":164896186,"end":164955525,"strand":-1,"description":"solute carrier family 38 member 11 [Source:HGNC Symbol;Acc:HGNC:26836]"}, {"versioned_ensembl_gene_id":"ENSG00000230043.1","gene_symbol":"TMSB4XP6","gene_name":"thymosin beta 4, X-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:11888]","synonyms":"TMSL6,TMSB4L,dJ1071L10.1","biotype":"processed_pseudogene","ncbi_id":"7120","summary":null,"start":50840615,"end":50840749,"strand":-1,"description":"thymosin beta 4, X-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:11888]"}, {"versioned_ensembl_gene_id":"ENSG00000258738.1","gene_symbol":"AL121603.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34874343,"end":34876459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105370.7","gene_symbol":"LIM2","gene_name":"lens intrinsic membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:6610]","synonyms":"MP19,MP17","biotype":"protein_coding","ncbi_id":"3982","summary":"This gene encodes an eye lens-specific protein found at the junctions of lens fiber cells, where it may contribute to cell junctional organization. It acts as a receptor for calmodulin, and may play an important role in both lens development and cataractogenesis. Mutations in this gene have been associated with cataract formation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":51379909,"end":51387960,"strand":-1,"description":"lens intrinsic membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:6610]"}, {"versioned_ensembl_gene_id":"ENSG00000065491.8","gene_symbol":"TBC1D22B","gene_name":"TBC1 domain family member 22B [Source:HGNC Symbol;Acc:HGNC:21602]","synonyms":"FLJ20337,dJ744I24.2,C6orf197","biotype":"protein_coding","ncbi_id":"55633","summary":null,"start":37257772,"end":37332970,"strand":1,"description":"TBC1 domain family member 22B [Source:HGNC Symbol;Acc:HGNC:21602]"}, {"versioned_ensembl_gene_id":"ENSG00000197136.4","gene_symbol":"PCNX3","gene_name":"pecanex homolog 3 [Source:HGNC Symbol;Acc:HGNC:18760]","synonyms":"PCNXL3,FLJ22427","biotype":"protein_coding","ncbi_id":"399909","summary":null,"start":65615773,"end":65637439,"strand":1,"description":"pecanex homolog 3 [Source:HGNC Symbol;Acc:HGNC:18760]"}, {"versioned_ensembl_gene_id":"ENSG00000275550.1","gene_symbol":"AL096712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37295584,"end":37295742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117877.10","gene_symbol":"CD3EAP","gene_name":"CD3e molecule associated protein [Source:HGNC Symbol;Acc:HGNC:24219]","synonyms":"PAF49,CAST,ASE-1","biotype":"protein_coding","ncbi_id":"10849","summary":null,"start":45406209,"end":45410766,"strand":1,"description":"CD3e molecule associated protein [Source:HGNC Symbol;Acc:HGNC:24219]"}, {"versioned_ensembl_gene_id":"ENSG00000172738.11","gene_symbol":"TMEM217","gene_name":"transmembrane protein 217 [Source:HGNC Symbol;Acc:HGNC:21238]","synonyms":"dJ355M6.2,C6orf128","biotype":"protein_coding","ncbi_id":"221468","summary":null,"start":37212180,"end":37258155,"strand":-1,"description":"transmembrane protein 217 [Source:HGNC Symbol;Acc:HGNC:21238]"}, {"versioned_ensembl_gene_id":"ENSG00000138028.15","gene_symbol":"CGREF1","gene_name":"cell growth regulator with EF-hand domain 1 [Source:HGNC Symbol;Acc:HGNC:16962]","synonyms":"CGR11","biotype":"protein_coding","ncbi_id":"10669","summary":null,"start":27098889,"end":27119115,"strand":-1,"description":"cell growth regulator with EF-hand domain 1 [Source:HGNC Symbol;Acc:HGNC:16962]"}, {"versioned_ensembl_gene_id":"ENSG00000270487.1","gene_symbol":"AL355297.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156780327,"end":156780455,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233825.1","gene_symbol":"AL391839.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32346499,"end":32347179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250026.5","gene_symbol":"TMPRSS11BNL","gene_name":"TMPRSS11B N-terminal like, pseudogene [Source:HGNC Symbol;Acc:HGNC:37262]","synonyms":"FLJ41562","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401136","summary":null,"start":68184081,"end":68218080,"strand":-1,"description":"TMPRSS11B N-terminal like, pseudogene [Source:HGNC Symbol;Acc:HGNC:37262]"}, {"versioned_ensembl_gene_id":"ENSG00000244515.1","gene_symbol":"KRT18P34","gene_name":"keratin 18 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:33403]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391589","summary":null,"start":157162663,"end":157163932,"strand":-1,"description":"keratin 18 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:33403]"}, {"versioned_ensembl_gene_id":"ENSG00000166188.2","gene_symbol":"ZNF319","gene_name":"zinc finger protein 319 [Source:HGNC Symbol;Acc:HGNC:13644]","synonyms":"Zfp319,KIAA1388","biotype":"protein_coding","ncbi_id":"57567","summary":null,"start":57994668,"end":58000453,"strand":-1,"description":"zinc finger protein 319 [Source:HGNC Symbol;Acc:HGNC:13644]"}, {"versioned_ensembl_gene_id":"ENSG00000241770.1","gene_symbol":"AC104411.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157163452,"end":157169133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257553.1","gene_symbol":"AC034102.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56104614,"end":56113905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184451.5","gene_symbol":"CCR10","gene_name":"C-C motif chemokine receptor 10 [Source:HGNC Symbol;Acc:HGNC:4474]","synonyms":"GPR2","biotype":"protein_coding","ncbi_id":"2826","summary":"Chemokines are a group of small (approximately 8 to 14 kD), mostly basic, structurally related molecules that regulate cell trafficking of various types of leukocytes through interactions with a subset of 7-transmembrane, G protein-coupled receptors. Chemokines also play fundamental roles in the development, homeostasis, and function of the immune system, and they have effects on cells of the central nervous system as well as on endothelial cells involved in angiogenesis or angiostasis. Chemokines are divided into 2 major subfamilies, CXC and CC, based on the arrangement of the first 2 of the 4 conserved cysteine residues; the 2 cysteines are separated by a single amino acid in CXC chemokines and are adjacent in CC chemokines. CCR10 is the receptor for CCL27 (SCYA27; MIM 604833); CCR10-CCL27 interactions are involved in T cell-mediated skin inflammation (Homey et al., 2002 [PubMed 11821900]).[supplied by OMIM, Mar 2008]","start":42678889,"end":42683917,"strand":-1,"description":"C-C motif chemokine receptor 10 [Source:HGNC Symbol;Acc:HGNC:4474]"}, {"versioned_ensembl_gene_id":"ENSG00000049618.22","gene_symbol":"ARID1B","gene_name":"AT-rich interaction domain 1B [Source:HGNC Symbol;Acc:HGNC:18040]","synonyms":"p250R,KIAA1235,ELD/OSA1,DAN15,BAF250b,6A3-5","biotype":"protein_coding","ncbi_id":"57492","summary":"This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":156777374,"end":157210779,"strand":1,"description":"AT-rich interaction domain 1B [Source:HGNC Symbol;Acc:HGNC:18040]"}, {"versioned_ensembl_gene_id":"ENSG00000211455.7","gene_symbol":"STK38L","gene_name":"serine/threonine kinase 38 like [Source:HGNC Symbol;Acc:HGNC:17848]","synonyms":"NDR2,KIAA0965","biotype":"protein_coding","ncbi_id":"23012","summary":null,"start":27243968,"end":27325959,"strand":1,"description":"serine/threonine kinase 38 like [Source:HGNC Symbol;Acc:HGNC:17848]"}, {"versioned_ensembl_gene_id":"ENSG00000227433.1","gene_symbol":"AC090018.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195349664,"end":195350030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189120.4","gene_symbol":"SP6","gene_name":"Sp6 transcription factor [Source:HGNC Symbol;Acc:HGNC:14530]","synonyms":"KLF14,Epfn","biotype":"protein_coding","ncbi_id":"80320","summary":"SP6 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]","start":47844908,"end":47855874,"strand":-1,"description":"Sp6 transcription factor [Source:HGNC Symbol;Acc:HGNC:14530]"}, {"versioned_ensembl_gene_id":"ENSG00000229325.1","gene_symbol":"ACAP2-IT1","gene_name":"ACAP2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41426]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874306","summary":null,"start":195280723,"end":195282741,"strand":-1,"description":"ACAP2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41426]"}, {"versioned_ensembl_gene_id":"ENSG00000267042.1","gene_symbol":"AC100793.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42679963,"end":42682020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114331.13","gene_symbol":"ACAP2","gene_name":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 [Source:HGNC Symbol;Acc:HGNC:16469]","synonyms":"KIAA0041,CNT-B2,CENTB2","biotype":"protein_coding","ncbi_id":"23527","summary":null,"start":195274736,"end":195443078,"strand":-1,"description":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 [Source:HGNC Symbol;Acc:HGNC:16469]"}, {"versioned_ensembl_gene_id":"ENSG00000282943.1","gene_symbol":"AC004784.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42977463,"end":43171515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125740.13","gene_symbol":"FOSB","gene_name":"FosB proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3797]","synonyms":"MGC42291,GOSB,GOS3,G0S3,DKFZp686C0818,AP-1","biotype":"protein_coding","ncbi_id":"2354","summary":"The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":45467995,"end":45475179,"strand":1,"description":"FosB proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3797]"}, {"versioned_ensembl_gene_id":"ENSG00000262874.1","gene_symbol":"C19orf84","gene_name":"chromosome 19 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:27112]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147646","summary":null,"start":51388289,"end":51390574,"strand":-1,"description":"chromosome 19 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:27112]"}, {"versioned_ensembl_gene_id":"ENSG00000243137.7","gene_symbol":"PSG4","gene_name":"pregnancy specific beta-1-glycoprotein 4 [Source:HGNC Symbol;Acc:HGNC:9521]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5672","summary":"The protein encoded by this gene is a pregnancy-specific glycoprotein (PSG), one of several encoded by a cluster of similar genes on chromosome 19. This gene is a member of the carcinoembryonic antigen (CEA) gene family and may play a role in regulation of the innate immune system. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":43192702,"end":43207299,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 4 [Source:HGNC Symbol;Acc:HGNC:9521]"}, {"versioned_ensembl_gene_id":"ENSG00000163239.12","gene_symbol":"TDRD10","gene_name":"tudor domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25316]","synonyms":"DKFZp434M202","biotype":"protein_coding","ncbi_id":"126668","summary":null,"start":154502219,"end":154548147,"strand":1,"description":"tudor domain containing 10 [Source:HGNC Symbol;Acc:HGNC:25316]"}, {"versioned_ensembl_gene_id":"ENSG00000264243.1","gene_symbol":"AC018521.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47863342,"end":47865190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268889.1","gene_symbol":"AC008750.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51394488,"end":51403650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268144.1","gene_symbol":"NIFKP6","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44954]","synonyms":"MKI67IPP6","biotype":"processed_pseudogene","ncbi_id":"100132796","summary":null,"start":51396755,"end":51403526,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44954]"}, {"versioned_ensembl_gene_id":"ENSG00000266821.1","gene_symbol":"AC018521.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47879472,"end":47882398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044090.8","gene_symbol":"CUL7","gene_name":"cullin 7 [Source:HGNC Symbol;Acc:HGNC:21024]","synonyms":"KIAA0076,dJ20C7.5","biotype":"protein_coding","ncbi_id":"9820","summary":"The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":43037617,"end":43053945,"strand":-1,"description":"cullin 7 [Source:HGNC Symbol;Acc:HGNC:21024]"}, {"versioned_ensembl_gene_id":"ENSG00000178226.10","gene_symbol":"PRSS36","gene_name":"protease, serine 36 [Source:HGNC Symbol;Acc:HGNC:26906]","synonyms":"FLJ90661","biotype":"protein_coding","ncbi_id":"146547","summary":null,"start":31138925,"end":31150094,"strand":-1,"description":"protease, serine 36 [Source:HGNC Symbol;Acc:HGNC:26906]"}, {"versioned_ensembl_gene_id":"ENSG00000255647.3","gene_symbol":"AC093510.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":90410000,"end":90410669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264920.1","gene_symbol":"AC018521.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":47891255,"end":47895812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232809.1","gene_symbol":"VDAC1P10","gene_name":"voltage dependent anion channel 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37479]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643536","summary":null,"start":215376484,"end":215377374,"strand":1,"description":"voltage dependent anion channel 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37479]"}, {"versioned_ensembl_gene_id":"ENSG00000230176.2","gene_symbol":"LINC01433","gene_name":"long intergenic non-protein coding RNA 1433 [Source:HGNC Symbol;Acc:HGNC:50746]","synonyms":"LOC728228","biotype":"antisense_RNA","ncbi_id":"728228","summary":null,"start":4193065,"end":4195943,"strand":1,"description":"long intergenic non-protein coding RNA 1433 [Source:HGNC Symbol;Acc:HGNC:50746]"}, {"versioned_ensembl_gene_id":"ENSG00000227253.3","gene_symbol":"AL158834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32266289,"end":32269474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234494.7","gene_symbol":"SP2-AS1","gene_name":"SP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51341]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506325","summary":null,"start":47897330,"end":47941410,"strand":-1,"description":"SP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51341]"}, {"versioned_ensembl_gene_id":"ENSG00000170515.13","gene_symbol":"PA2G4","gene_name":"proliferation-associated 2G4 [Source:HGNC Symbol;Acc:HGNC:8550]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5036","summary":"This gene encodes an RNA-binding protein that is involved in growth regulation. This protein is present in pre-ribosomal ribonucleoprotein complexes and may be involved in ribosome assembly and the regulation of intermediate and late steps of rRNA processing. This protein can interact with the cytoplasmic domain of the ErbB3 receptor and may contribute to transducing growth regulatory signals. This protein is also a transcriptional co-repressor of androgen receptor-regulated genes and other cell cycle regulatory genes through its interactions with histone deacetylases. This protein has been implicated in growth inhibition and the induction of differentiation of human cancer cells. Six pseudogenes, located on chromosomes 3, 6, 9, 18, 20 and X, have been identified. [provided by RefSeq, Jul 2008]","start":56104319,"end":56113907,"strand":1,"description":"proliferation-associated 2G4 [Source:HGNC Symbol;Acc:HGNC:8550]"}, {"versioned_ensembl_gene_id":"ENSG00000113356.11","gene_symbol":"POLR3G","gene_name":"RNA polymerase III subunit G [Source:HGNC Symbol;Acc:HGNC:30075]","synonyms":"RPC7,RPC32","biotype":"protein_coding","ncbi_id":"10622","summary":null,"start":90471748,"end":90514553,"strand":1,"description":"RNA polymerase III subunit G [Source:HGNC Symbol;Acc:HGNC:30075]"}, {"versioned_ensembl_gene_id":"ENSG00000266601.1","gene_symbol":"AC018521.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47929682,"end":47933106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224331.2","gene_symbol":"AC019181.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164687287,"end":164687596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171873.7","gene_symbol":"ADRA1D","gene_name":"adrenoceptor alpha 1D [Source:HGNC Symbol;Acc:HGNC:280]","synonyms":"ADRA1R,ADRA1A,ADRA1","biotype":"protein_coding","ncbi_id":"146","summary":"Alpha-1-adrenergic receptors (alpha-1-ARs) are members of the G protein-coupled receptor superfamily. They activate mitogenic responses and regulate growth and proliferation of many cells. There are 3 alpha-1-AR subtypes: alpha-1A, -1B and -1D, all of which signal through the Gq/11 family of G-proteins and different subtypes show different patterns of activation. This gene encodes alpha-1D-adrenergic receptor. Similar to alpha-1B-adrenergic receptor gene, this gene comprises 2 exons and a single intron that interrupts the coding region. [provided by RefSeq, Jul 2008]","start":4220631,"end":4249074,"strand":-1,"description":"adrenoceptor alpha 1D [Source:HGNC Symbol;Acc:HGNC:280]"}, {"versioned_ensembl_gene_id":"ENSG00000278400.1","gene_symbol":"AC026120.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56941174,"end":56941482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130881.13","gene_symbol":"LRP3","gene_name":"LDL receptor related protein 3 [Source:HGNC Symbol;Acc:HGNC:6695]","synonyms":"LRP-3,hLRp105","biotype":"protein_coding","ncbi_id":"4037","summary":null,"start":33177603,"end":33208867,"strand":1,"description":"LDL receptor related protein 3 [Source:HGNC Symbol;Acc:HGNC:6695]"}, {"versioned_ensembl_gene_id":"ENSG00000167182.14","gene_symbol":"SP2","gene_name":"Sp2 transcription factor [Source:HGNC Symbol;Acc:HGNC:11207]","synonyms":"KIAA0048","biotype":"protein_coding","ncbi_id":"6668","summary":"This gene encodes a member of the Sp subfamily of Sp/XKLF transcription factors. Sp family proteins are sequence-specific DNA-binding proteins characterized by an amino-terminal trans-activation domain and three carboxy-terminal zinc finger motifs. This protein contains the least conserved DNA-binding domain within the Sp subfamily of proteins, and its DNA sequence specificity differs from the other Sp proteins. It localizes primarily within subnuclear foci associated with the nuclear matrix, and can activate or in some cases repress expression from different promoters. [provided by RefSeq, Jul 2008]","start":47896150,"end":47928957,"strand":1,"description":"Sp2 transcription factor [Source:HGNC Symbol;Acc:HGNC:11207]"}, {"versioned_ensembl_gene_id":"ENSG00000198590.11","gene_symbol":"C3orf35","gene_name":"chromosome 3 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:24082]","synonyms":"APRG1","biotype":"protein_coding","ncbi_id":"339883","summary":null,"start":37386269,"end":37435497,"strand":1,"description":"chromosome 3 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:24082]"}, {"versioned_ensembl_gene_id":"ENSG00000213312.3","gene_symbol":"AL135905.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63548708,"end":63549508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266680.1","gene_symbol":"AL135905.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63571005,"end":63572408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082438.15","gene_symbol":"COBLL1","gene_name":"cordon-bleu WH2 repeat protein like 1 [Source:HGNC Symbol;Acc:HGNC:23571]","synonyms":"KIAA0977","biotype":"protein_coding","ncbi_id":"22837","summary":null,"start":164653624,"end":164843679,"strand":-1,"description":"cordon-bleu WH2 repeat protein like 1 [Source:HGNC Symbol;Acc:HGNC:23571]"}, {"versioned_ensembl_gene_id":"ENSG00000112245.10","gene_symbol":"PTP4A1","gene_name":"protein tyrosine phosphatase type IVA, member 1 [Source:HGNC Symbol;Acc:HGNC:9634]","synonyms":"PTPCAAX1,PRL-1","biotype":"protein_coding","ncbi_id":"7803","summary":"This gene encodes a member of a small class of prenylated protein tyrosine phosphatases (PTPs), which contain a PTP domain and a characteristic C-terminal prenylation motif. The encoded protein is a cell signaling molecule that plays regulatory roles in a variety of cellular processes, including cell proliferation and migration. The protein may also be involved in cancer development and metastasis. This tyrosine phosphatase is a nuclear protein, but may associate with plasma membrane by means of its prenylation motif. Pseudogenes related to this gene are located on chromosomes 1, 2, 5, 7, 11 and X. [provided by RefSeq, Jun 2013]","start":63521748,"end":63583587,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 [Source:HGNC Symbol;Acc:HGNC:9634]"}, {"versioned_ensembl_gene_id":"ENSG00000133641.17","gene_symbol":"C12orf29","gene_name":"chromosome 12 open reading frame 29 [Source:HGNC Symbol;Acc:HGNC:25322]","synonyms":"DKFZp434N2030","biotype":"protein_coding","ncbi_id":"91298","summary":null,"start":88033846,"end":88050160,"strand":1,"description":"chromosome 12 open reading frame 29 [Source:HGNC Symbol;Acc:HGNC:25322]"}, {"versioned_ensembl_gene_id":"ENSG00000031691.6","gene_symbol":"CENPQ","gene_name":"centromere protein Q [Source:HGNC Symbol;Acc:HGNC:21347]","synonyms":"FLJ10545,CENP-Q,C6orf139","biotype":"protein_coding","ncbi_id":"55166","summary":"CENPQ is a subunit of a CENPH (MIM 605607)-CENPI (MIM 300065)-associated centromeric complex that targets CENPA (MIM 117139) to centromeres and is required for proper kinetochore function and mitotic progression (Okada et al., 2006 [PubMed 16622420]).[supplied by OMIM, Mar 2008]","start":49463378,"end":49493107,"strand":1,"description":"centromere protein Q [Source:HGNC Symbol;Acc:HGNC:21347]"}, {"versioned_ensembl_gene_id":"ENSG00000258541.1","gene_symbol":"OR4K4P","gene_name":"olfactory receptor family 4 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14744]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79318","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19905917,"end":19906600,"strand":1,"description":"olfactory receptor family 4 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14744]"}, {"versioned_ensembl_gene_id":"ENSG00000275763.3","gene_symbol":"C18orf65","gene_name":"chromosome 18 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:51248]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400658","summary":null,"start":76495521,"end":76498088,"strand":1,"description":"chromosome 18 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:51248]"}, {"versioned_ensembl_gene_id":"ENSG00000259847.1","gene_symbol":"LINC02126","gene_name":"long intergenic non-protein coding RNA 2126 [Source:HGNC Symbol;Acc:HGNC:52983]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927650","summary":null,"start":65141756,"end":65176713,"strand":-1,"description":"long intergenic non-protein coding RNA 2126 [Source:HGNC Symbol;Acc:HGNC:52983]"}, {"versioned_ensembl_gene_id":"ENSG00000273763.1","gene_symbol":"AC007318.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65203571,"end":65203813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259016.1","gene_symbol":"AL391156.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19908096,"end":19908649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283977.1","gene_symbol":"AC084337.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6481485,"end":6508978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172974.11","gene_symbol":"AC007318.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65205108,"end":65205988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267714.1","gene_symbol":"AC008738.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33217817,"end":33221170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263812.5","gene_symbol":"LINC00908","gene_name":"long intergenic non-protein coding RNA 908 [Source:HGNC Symbol;Acc:HGNC:27599]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284276","summary":null,"start":76528655,"end":76610968,"strand":1,"description":"long intergenic non-protein coding RNA 908 [Source:HGNC Symbol;Acc:HGNC:27599]"}, {"versioned_ensembl_gene_id":"ENSG00000130876.11","gene_symbol":"SLC7A10","gene_name":"solute carrier family 7 member 10 [Source:HGNC Symbol;Acc:HGNC:11058]","synonyms":"asc-1","biotype":"protein_coding","ncbi_id":"56301","summary":"SLC7A10, in association with 4F2HC (SLC3A2; MIM 158070), mediates high-affinity transport of D-serine and several other neutral amino acids (Nakauchi et al., 2000 [PubMed 10863037]).[supplied by OMIM, Mar 2008]","start":33208664,"end":33225850,"strand":-1,"description":"solute carrier family 7 member 10 [Source:HGNC Symbol;Acc:HGNC:11058]"}, {"versioned_ensembl_gene_id":"ENSG00000228713.1","gene_symbol":"CR759828.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31384925,"end":31385659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261742.5","gene_symbol":"LINC00922","gene_name":"long intergenic non-protein coding RNA 922 [Source:HGNC Symbol;Acc:HGNC:27545]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283867","summary":null,"start":65284499,"end":65576300,"strand":-1,"description":"long intergenic non-protein coding RNA 922 [Source:HGNC Symbol;Acc:HGNC:27545]"}, {"versioned_ensembl_gene_id":"ENSG00000226050.3","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"KIAA0055-hom,D84394.7,USP8P","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31352684,"end":31355856,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000179532.12","gene_symbol":"DNHD1","gene_name":"dynein heavy chain domain 1 [Source:HGNC Symbol;Acc:HGNC:26532]","synonyms":"DKFZp686J0796,DHCD1,CCDC35,C11orf47,FLJ46184,FLJ35709,FLJ32752,DNHD1L","biotype":"protein_coding","ncbi_id":"144132","summary":null,"start":6497260,"end":6593758,"strand":1,"description":"dynein heavy chain domain 1 [Source:HGNC Symbol;Acc:HGNC:26532]"}, {"versioned_ensembl_gene_id":"ENSG00000227656.3","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31357419,"end":31358618,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000232126.8","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31346626,"end":31433637,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000253583.1","gene_symbol":"AC018953.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63586000,"end":63589408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197415.11","gene_symbol":"VEPH1","gene_name":"ventricular zone expressed PH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25735]","synonyms":"KIAA1692,FLJ12604","biotype":"protein_coding","ncbi_id":"79674","summary":null,"start":157259742,"end":157533619,"strand":-1,"description":"ventricular zone expressed PH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25735]"}, {"versioned_ensembl_gene_id":"ENSG00000131379.9","gene_symbol":"C3orf20","gene_name":"chromosome 3 open reading frame 20 [Source:HGNC Symbol;Acc:HGNC:25320]","synonyms":"DKFZP434N1817","biotype":"protein_coding","ncbi_id":"84077","summary":null,"start":14675099,"end":14773034,"strand":1,"description":"chromosome 3 open reading frame 20 [Source:HGNC Symbol;Acc:HGNC:25320]"}, {"versioned_ensembl_gene_id":"ENSG00000171199.10","gene_symbol":"OPRPN","gene_name":"opiorphin prepropeptide [Source:HGNC Symbol;Acc:HGNC:17279]","synonyms":"PROL1,PRL1,BPLP","biotype":"protein_coding","ncbi_id":"58503","summary":"This gene encodes a member of the proline-rich protein family. The encoded protein has multiple proposed functions, including roles in pain suppression, penile erection, and protection of the eye surface. The QRFSR pentapeptide, known as opiorphin, is derived from the N-terminal of this protein. Opiorphin inhibits the enkephalin-inactivating peptidases neprilysin and aminopeptidase N, and this activity is thought to reduce sensitivity to painful stimuli by effecting enkephalin-related activation of opioid-dependent pathways. Opiorphin may also act as an anti-depressant. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":70397882,"end":70410194,"strand":1,"description":"opiorphin prepropeptide [Source:HGNC Symbol;Acc:HGNC:17279]"}, {"versioned_ensembl_gene_id":"ENSG00000260364.1","gene_symbol":"AC009055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65233056,"end":65432820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260834.1","gene_symbol":"AC009055.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65190973,"end":65234914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253762.1","gene_symbol":"AC069133.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63704756,"end":63751677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000031003.10","gene_symbol":"FAM13B","gene_name":"family with sequence similarity 13 member B [Source:HGNC Symbol;Acc:HGNC:1335]","synonyms":"N61,KHCHP,FAM13B1,C5orf5,ARHGAP49","biotype":"protein_coding","ncbi_id":"51306","summary":null,"start":137937960,"end":138051961,"strand":-1,"description":"family with sequence similarity 13 member B [Source:HGNC Symbol;Acc:HGNC:1335]"}, {"versioned_ensembl_gene_id":"ENSG00000253554.5","gene_symbol":"AC022639.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63687179,"end":64368558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176281.4","gene_symbol":"OR4K5","gene_name":"olfactory receptor family 4 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:14745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79317","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19920582,"end":19921659,"strand":1,"description":"olfactory receptor family 4 subfamily K member 5 [Source:HGNC Symbol;Acc:HGNC:14745]"}, {"versioned_ensembl_gene_id":"ENSG00000012061.15","gene_symbol":"ERCC1","gene_name":"ERCC excision repair 1, endonuclease non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:3433]","synonyms":"RAD10","biotype":"protein_coding","ncbi_id":"2067","summary":"The product of this gene functions in the nucleotide excision repair pathway, and is required for the repair of DNA lesions such as those induced by UV light or formed by electrophilic compounds including cisplatin. The encoded protein forms a heterodimer with the XPF endonuclease (also known as ERCC4), and the heterodimeric endonuclease catalyzes the 5' incision in the process of excising the DNA lesion. The heterodimeric endonuclease is also involved in recombinational DNA repair and in the repair of inter-strand crosslinks. Mutations in this gene result in cerebrooculofacioskeletal syndrome, and polymorphisms that alter expression of this gene may play a role in carcinogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. The last exon of this gene overlaps with the CD3e molecule, epsilon associated protein gene on the opposite strand. [provided by RefSeq, Oct 2009]","start":45407333,"end":45478828,"strand":-1,"description":"ERCC excision repair 1, endonuclease non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:3433]"}, {"versioned_ensembl_gene_id":"ENSG00000277186.1","gene_symbol":"AC131212.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132593031,"end":132593698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221716.1","gene_symbol":"SNORA11","gene_name":"small nucleolar RNA, H/ACA box 11 [Source:HGNC Symbol;Acc:HGNC:32599]","synonyms":"U107,SNORA11A","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":54814370,"end":54814497,"strand":1,"description":"small nucleolar RNA, H/ACA box 11 [Source:HGNC Symbol;Acc:HGNC:32599]"}, {"versioned_ensembl_gene_id":"ENSG00000222750.1","gene_symbol":"RNU4-46P","gene_name":"RNA, U4 small nuclear 46, pseudogene [Source:HGNC Symbol;Acc:HGNC:46982]","synonyms":null,"biotype":"snRNA","ncbi_id":"107048985","summary":null,"start":19498610,"end":19498747,"strand":1,"description":"RNA, U4 small nuclear 46, pseudogene [Source:HGNC Symbol;Acc:HGNC:46982]"}, {"versioned_ensembl_gene_id":"ENSG00000110429.13","gene_symbol":"FBXO3","gene_name":"F-box protein 3 [Source:HGNC Symbol;Acc:HGNC:13582]","synonyms":"FBX3,FBA","biotype":"protein_coding","ncbi_id":"26273","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Alternative splicing of this gene generates 2 transcript variants diverging at the 3' end. [provided by RefSeq, Jul 2008]","start":33740939,"end":33774543,"strand":-1,"description":"F-box protein 3 [Source:HGNC Symbol;Acc:HGNC:13582]"}, {"versioned_ensembl_gene_id":"ENSG00000138604.9","gene_symbol":"GLCE","gene_name":"glucuronic acid epimerase [Source:HGNC Symbol;Acc:HGNC:17855]","synonyms":"KIAA0836,HSEPI","biotype":"protein_coding","ncbi_id":"26035","summary":null,"start":69160584,"end":69272217,"strand":1,"description":"glucuronic acid epimerase [Source:HGNC Symbol;Acc:HGNC:17855]"}, {"versioned_ensembl_gene_id":"ENSG00000227806.1","gene_symbol":"OR5W1P","gene_name":"olfactory receptor family 5 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15298]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81182","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55903341,"end":55904278,"strand":-1,"description":"olfactory receptor family 5 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15298]"}, {"versioned_ensembl_gene_id":"ENSG00000253734.1","gene_symbol":"LINC01289","gene_name":"long intergenic non-protein coding RNA 1289 [Source:HGNC Symbol;Acc:HGNC:50354]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286184","summary":null,"start":63769430,"end":63785501,"strand":1,"description":"long intergenic non-protein coding RNA 1289 [Source:HGNC Symbol;Acc:HGNC:50354]"}, {"versioned_ensembl_gene_id":"ENSG00000236932.2","gene_symbol":"CEACAMP8","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:1830]","synonyms":"CGM15","biotype":"unprocessed_pseudogene","ncbi_id":"1096","summary":null,"start":43035869,"end":43041248,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:1830]"}, {"versioned_ensembl_gene_id":"ENSG00000176055.9","gene_symbol":"MBLAC2","gene_name":"metallo-beta-lactamase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33711]","synonyms":"MGC46734,DKFZp686P15118","biotype":"protein_coding","ncbi_id":"153364","summary":null,"start":90458203,"end":90474768,"strand":-1,"description":"metallo-beta-lactamase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33711]"}, {"versioned_ensembl_gene_id":"ENSG00000253231.1","gene_symbol":"COX6CP8","gene_name":"cytochrome c oxidase subunit 6C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481680","summary":null,"start":64331927,"end":64332152,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49360]"}, {"versioned_ensembl_gene_id":"ENSG00000243130.7","gene_symbol":"PSG11","gene_name":"pregnancy specific beta-1-glycoprotein 11 [Source:HGNC Symbol;Acc:HGNC:9516]","synonyms":"PSG14,PSG13,MGC22484","biotype":"protein_coding","ncbi_id":"5680","summary":"The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":43007656,"end":43026512,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 11 [Source:HGNC Symbol;Acc:HGNC:9516]"}, {"versioned_ensembl_gene_id":"ENSG00000132702.12","gene_symbol":"HAPLN2","gene_name":"hyaluronan and proteoglycan link protein 2 [Source:HGNC Symbol;Acc:HGNC:17410]","synonyms":"BRAL1","biotype":"protein_coding","ncbi_id":"60484","summary":null,"start":156619294,"end":156625725,"strand":1,"description":"hyaluronan and proteoglycan link protein 2 [Source:HGNC Symbol;Acc:HGNC:17410]"}, {"versioned_ensembl_gene_id":"ENSG00000204583.9","gene_symbol":"LRCOL1","gene_name":"leucine rich colipase like 1 [Source:HGNC Symbol;Acc:HGNC:44160]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507055","summary":null,"start":132603150,"end":132610543,"strand":-1,"description":"leucine rich colipase like 1 [Source:HGNC Symbol;Acc:HGNC:44160]"}, {"versioned_ensembl_gene_id":"ENSG00000282265.1","gene_symbol":"AL450990.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215393646,"end":215394418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273420.1","gene_symbol":"AC008738.7","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":33207129,"end":33207639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267054.1","gene_symbol":"AC008738.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33178056,"end":33178651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168615.11","gene_symbol":"ADAM9","gene_name":"ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:HGNC:216]","synonyms":"CORD9,Mltng,MDC9,MCMP,KIAA0021","biotype":"protein_coding","ncbi_id":"8754","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene interacts with SH3 domain-containing proteins, binds mitotic arrest deficient 2 beta protein, and is also involved in TPA-induced ectodomain shedding of membrane-anchored heparin-binding EGF-like growth factor. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2010]","start":38996869,"end":39105144,"strand":1,"description":"ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:HGNC:216]"}, {"versioned_ensembl_gene_id":"ENSG00000237833.1","gene_symbol":"AL391380.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135583651,"end":135585160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172345.13","gene_symbol":"STARD5","gene_name":"StAR related lipid transfer domain containing 5 [Source:HGNC Symbol;Acc:HGNC:18065]","synonyms":"MGC10327","biotype":"protein_coding","ncbi_id":"80765","summary":"Proteins containing a steroidogenic acute regulatory-related lipid transfer (START) domain are often involved in the trafficking of lipids and cholesterol between diverse intracellular membranes. This gene is a member of the StarD subfamily that encodes START-related lipid transfer proteins. The protein encoded by this gene is a cholesterol transporter and is also able to bind and transport other sterol-derived molecules related to the cholesterol/bile acid biosynthetic pathways such as 25-hydroxycholesterol. Its expression is upregulated during endoplasmic reticulum (ER) stress. The protein is thought to act as a cytosolic sterol transporter that moves cholesterol between intracellular membranes such as from the cytoplasm to the ER and from the ER to the Golgi apparatus. Alternative splicing of this gene produces multiple transcript variants. [provided by RefSeq, Jan 2016]","start":81309053,"end":81324183,"strand":-1,"description":"StAR related lipid transfer domain containing 5 [Source:HGNC Symbol;Acc:HGNC:18065]"}, {"versioned_ensembl_gene_id":"ENSG00000167494.9","gene_symbol":"NOS2P2","gene_name":"nitric oxide synthase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7874]","synonyms":"NOS2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"201288","summary":null,"start":18497095,"end":18506313,"strand":-1,"description":"nitric oxide synthase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7874]"}, {"versioned_ensembl_gene_id":"ENSG00000278172.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29864372,"end":29864629,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201433.1","gene_symbol":"RNU6-335P","gene_name":"RNA, U6 small nuclear 335, pseudogene [Source:HGNC Symbol;Acc:HGNC:47298]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479715","summary":null,"start":183675603,"end":183675715,"strand":-1,"description":"RNA, U6 small nuclear 335, pseudogene [Source:HGNC Symbol;Acc:HGNC:47298]"}, {"versioned_ensembl_gene_id":"ENSG00000199293.1","gene_symbol":"SNORA21","gene_name":"small nucleolar RNA, H/ACA box 21 [Source:HGNC Symbol;Acc:HGNC:32611]","synonyms":"ACA21","biotype":"snoRNA","ncbi_id":"619505","summary":null,"start":38852863,"end":38852994,"strand":-1,"description":"small nucleolar RNA, H/ACA box 21 [Source:HGNC Symbol;Acc:HGNC:32611]"}, {"versioned_ensembl_gene_id":"ENSG00000207091.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34314728,"end":34314828,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265140.1","gene_symbol":"MIR4301","gene_name":"microRNA 4301 [Source:HGNC Symbol;Acc:HGNC:38323]","synonyms":"hsa-mir-4301","biotype":"miRNA","ncbi_id":"100422855","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113450023,"end":113450088,"strand":-1,"description":"microRNA 4301 [Source:HGNC Symbol;Acc:HGNC:38323]"}, {"versioned_ensembl_gene_id":"ENSG00000199961.1","gene_symbol":"SNORD1B","gene_name":"small nucleolar RNA, C/D box 1B [Source:HGNC Symbol;Acc:HGNC:32676]","synonyms":"snR38B,R38B","biotype":"snoRNA","ncbi_id":"677849","summary":null,"start":76561109,"end":76561192,"strand":1,"description":"small nucleolar RNA, C/D box 1B [Source:HGNC Symbol;Acc:HGNC:32676]"}, {"versioned_ensembl_gene_id":"ENSG00000283656.1","gene_symbol":"MIR4483","gene_name":"microRNA 4483 [Source:HGNC Symbol;Acc:HGNC:41761]","synonyms":"hsa-mir-4483","biotype":"miRNA","ncbi_id":"100616162","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113777993,"end":113778054,"strand":-1,"description":"microRNA 4483 [Source:HGNC Symbol;Acc:HGNC:41761]"}, {"versioned_ensembl_gene_id":"ENSG00000283534.1","gene_symbol":"MIR374C","gene_name":"microRNA 374c [Source:HGNC Symbol;Acc:HGNC:38907]","synonyms":"hsa-mir-374c","biotype":"miRNA","ncbi_id":"100500807","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74218549,"end":74218618,"strand":1,"description":"microRNA 374c [Source:HGNC Symbol;Acc:HGNC:38907]"}, {"versioned_ensembl_gene_id":"ENSG00000222490.1","gene_symbol":"RNU6-712P","gene_name":"RNA, U6 small nuclear 712, pseudogene [Source:HGNC Symbol;Acc:HGNC:47675]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481404","summary":null,"start":90184634,"end":90184733,"strand":1,"description":"RNA, U6 small nuclear 712, pseudogene [Source:HGNC Symbol;Acc:HGNC:47675]"}, {"versioned_ensembl_gene_id":"ENSG00000206718.1","gene_symbol":"RNU6-546P","gene_name":"RNA, U6 small nuclear 546, pseudogene [Source:HGNC Symbol;Acc:HGNC:47509]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479809","summary":null,"start":155330421,"end":155330527,"strand":1,"description":"RNA, U6 small nuclear 546, pseudogene [Source:HGNC Symbol;Acc:HGNC:47509]"}, {"versioned_ensembl_gene_id":"ENSG00000202001.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100755099,"end":100755195,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239821.3","gene_symbol":"RN7SL513P","gene_name":"RNA, 7SL, cytoplasmic 513, pseudogene [Source:HGNC Symbol;Acc:HGNC:46529]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481062","summary":null,"start":18333276,"end":18333573,"strand":1,"description":"RNA, 7SL, cytoplasmic 513, pseudogene [Source:HGNC Symbol;Acc:HGNC:46529]"}, {"versioned_ensembl_gene_id":"ENSG00000238965.1","gene_symbol":"RNA5SP351","gene_name":"RNA, 5S ribosomal pseudogene 351 [Source:HGNC Symbol;Acc:HGNC:43251]","synonyms":"RN5S351","biotype":"rRNA","ncbi_id":"106480764","summary":null,"start":111928400,"end":111928508,"strand":1,"description":"RNA, 5S ribosomal pseudogene 351 [Source:HGNC Symbol;Acc:HGNC:43251]"}, {"versioned_ensembl_gene_id":"ENSG00000272253.1","gene_symbol":"RNA5SP386","gene_name":"RNA, 5S ribosomal pseudogene 386 [Source:HGNC Symbol;Acc:HGNC:43286]","synonyms":"RN5S386","biotype":"rRNA","ncbi_id":"100873641","summary":null,"start":67657105,"end":67657211,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 386 [Source:HGNC Symbol;Acc:HGNC:43286]"}, {"versioned_ensembl_gene_id":"ENSG00000223330.1","gene_symbol":"RNU6-1052P","gene_name":"RNA, U6 small nuclear 1052, pseudogene [Source:HGNC Symbol;Acc:HGNC:48015]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480028","summary":null,"start":56402070,"end":56402173,"strand":-1,"description":"RNA, U6 small nuclear 1052, pseudogene [Source:HGNC Symbol;Acc:HGNC:48015]"}, {"versioned_ensembl_gene_id":"ENSG00000252742.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128350829,"end":128350927,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284394.1","gene_symbol":"MIR4750","gene_name":"microRNA 4750 [Source:HGNC Symbol;Acc:HGNC:41765]","synonyms":"hsa-mir-4750","biotype":"miRNA","ncbi_id":"100616314","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49888175,"end":49888230,"strand":1,"description":"microRNA 4750 [Source:HGNC Symbol;Acc:HGNC:41765]"}, {"versioned_ensembl_gene_id":"ENSG00000207959.1","gene_symbol":"MIR656","gene_name":"microRNA 656 [Source:HGNC Symbol;Acc:HGNC:32912]","synonyms":"MIRN656,hsa-mir-656","biotype":"miRNA","ncbi_id":"724026","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101066724,"end":101066801,"strand":1,"description":"microRNA 656 [Source:HGNC Symbol;Acc:HGNC:32912]"}, {"versioned_ensembl_gene_id":"ENSG00000278384.1","gene_symbol":"AL354822.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":51867,"end":54893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238399.1","gene_symbol":"MIR2053","gene_name":"microRNA 2053 [Source:HGNC Symbol;Acc:HGNC:37069]","synonyms":"hsa-mir-2053","biotype":"miRNA","ncbi_id":"100302225","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112643493,"end":112643583,"strand":1,"description":"microRNA 2053 [Source:HGNC Symbol;Acc:HGNC:37069]"}, {"versioned_ensembl_gene_id":"ENSG00000222182.1","gene_symbol":"RNA5SP156","gene_name":"RNA, 5S ribosomal pseudogene 156 [Source:HGNC Symbol;Acc:HGNC:43056]","synonyms":"RN5S156","biotype":"rRNA","ncbi_id":"100873422","summary":null,"start":11414051,"end":11414160,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 156 [Source:HGNC Symbol;Acc:HGNC:43056]"}, {"versioned_ensembl_gene_id":"ENSG00000207450.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47805079,"end":47805179,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206926.1","gene_symbol":"RNU6-1024P","gene_name":"RNA, U6 small nuclear 1024, pseudogene [Source:HGNC Symbol;Acc:HGNC:47987]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481504","summary":null,"start":15433110,"end":15433216,"strand":-1,"description":"RNA, U6 small nuclear 1024, pseudogene [Source:HGNC Symbol;Acc:HGNC:47987]"}, {"versioned_ensembl_gene_id":"ENSG00000206703.1","gene_symbol":"RNU6-128P","gene_name":"RNA, U6 small nuclear 128, pseudogene [Source:HGNC Symbol;Acc:HGNC:47091]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481217","summary":null,"start":158794590,"end":158794696,"strand":-1,"description":"RNA, U6 small nuclear 128, pseudogene [Source:HGNC Symbol;Acc:HGNC:47091]"}, {"versioned_ensembl_gene_id":"ENSG00000252115.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116909877,"end":116909964,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273904.1","gene_symbol":"Hammerhead_HH10","gene_name":"Hammerhead ribozyme HH10 [Source:RFAM;Acc:RF02277]","synonyms":null,"biotype":"ribozyme","ncbi_id":null,"summary":null,"start":114168156,"end":114168280,"strand":-1,"description":"Hammerhead ribozyme HH10 [Source:RFAM;Acc:RF02277]"}, {"versioned_ensembl_gene_id":"ENSG00000265539.1","gene_symbol":"MIR3164","gene_name":"microRNA 3164 [Source:HGNC Symbol;Acc:HGNC:38288]","synonyms":"hsa-mir-3164","biotype":"miRNA","ncbi_id":"100422846","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69083176,"end":69083258,"strand":1,"description":"microRNA 3164 [Source:HGNC Symbol;Acc:HGNC:38288]"}, {"versioned_ensembl_gene_id":"ENSG00000266228.1","gene_symbol":"MIR3611","gene_name":"microRNA 3611 [Source:HGNC Symbol;Acc:HGNC:38914]","synonyms":"hsa-mir-3611","biotype":"miRNA","ncbi_id":"100500890","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35079598,"end":35079680,"strand":-1,"description":"microRNA 3611 [Source:HGNC Symbol;Acc:HGNC:38914]"}, {"versioned_ensembl_gene_id":"ENSG00000281000.1","gene_symbol":"SNORD3D","gene_name":"small nucleolar RNA, C/D box 3D [Source:HGNC Symbol;Acc:HGNC:33192]","synonyms":"U3-4,RNU3-4,U3-4,RNU3-4","biotype":"snoRNA","ncbi_id":"780854","summary":null,"start":19112420,"end":19112636,"strand":-1,"description":"small nucleolar RNA, C/D box 3D [Source:HGNC Symbol;Acc:HGNC:33192]"}, {"versioned_ensembl_gene_id":"ENSG00000201609.1","gene_symbol":"RNU4-28P","gene_name":"RNA, U4 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46964]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479570","summary":null,"start":19510593,"end":19510733,"strand":1,"description":"RNA, U4 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:46964]"}, {"versioned_ensembl_gene_id":"ENSG00000265059.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32549943,"end":32550090,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000265456.1","gene_symbol":"MIR3672","gene_name":"microRNA 3672 [Source:HGNC Symbol;Acc:HGNC:38957]","synonyms":"hsa-mir-3672","biotype":"miRNA","ncbi_id":"100500869","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":121370972,"end":121371053,"strand":1,"description":"microRNA 3672 [Source:HGNC Symbol;Acc:HGNC:38957]"}, {"versioned_ensembl_gene_id":"ENSG00000284519.1","gene_symbol":"MIR6741","gene_name":"microRNA 6741 [Source:HGNC Symbol;Acc:HGNC:50004]","synonyms":"hsa-mir-6741","biotype":"miRNA","ncbi_id":"102466270","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":225922080,"end":225922142,"strand":-1,"description":"microRNA 6741 [Source:HGNC Symbol;Acc:HGNC:50004]"}, {"versioned_ensembl_gene_id":"ENSG00000278347.1","gene_symbol":"ZNRD1-AS1_1","gene_name":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30114397,"end":30114464,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02218]"}, {"versioned_ensembl_gene_id":"ENSG00000284277.1","gene_symbol":"MIR7162","gene_name":"microRNA 7162 [Source:HGNC Symbol;Acc:HGNC:50189]","synonyms":"hsa-mir-7162","biotype":"miRNA","ncbi_id":"102466227","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30368597,"end":30368665,"strand":-1,"description":"microRNA 7162 [Source:HGNC Symbol;Acc:HGNC:50189]"}, {"versioned_ensembl_gene_id":"ENSG00000202031.1","gene_symbol":"SNORD38A","gene_name":"small nucleolar RNA, C/D box 38A [Source:HGNC Symbol;Acc:HGNC:30355]","synonyms":"RNU38A,U38A","biotype":"snoRNA","ncbi_id":"94162","summary":null,"start":44777843,"end":44777912,"strand":1,"description":"small nucleolar RNA, C/D box 38A [Source:HGNC Symbol;Acc:HGNC:30355]"}, {"versioned_ensembl_gene_id":"ENSG00000201839.1","gene_symbol":"SNORD114-3","gene_name":"small nucleolar RNA, C/D box 114-3 [Source:HGNC Symbol;Acc:HGNC:32991]","synonyms":"14q(II-3)","biotype":"snoRNA","ncbi_id":"767579","summary":null,"start":100953349,"end":100953423,"strand":1,"description":"small nucleolar RNA, C/D box 114-3 [Source:HGNC Symbol;Acc:HGNC:32991]"}, {"versioned_ensembl_gene_id":"ENSG00000201065.1","gene_symbol":"RNU6-461P","gene_name":"RNA, U6 small nuclear 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:47424]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481897","summary":null,"start":102755064,"end":102755170,"strand":-1,"description":"RNA, U6 small nuclear 461, pseudogene [Source:HGNC Symbol;Acc:HGNC:47424]"}, {"versioned_ensembl_gene_id":"ENSG00000200987.1","gene_symbol":"SNORD115-30","gene_name":"small nucleolar RNA, C/D box 115-30 [Source:HGNC Symbol;Acc:HGNC:33049]","synonyms":"HBII-52-30","biotype":"snoRNA","ncbi_id":"100033804","summary":null,"start":25225203,"end":25225284,"strand":1,"description":"small nucleolar RNA, C/D box 115-30 [Source:HGNC Symbol;Acc:HGNC:33049]"}, {"versioned_ensembl_gene_id":"ENSG00000222344.1","gene_symbol":"RNU6-613P","gene_name":"RNA, U6 small nuclear 613, pseudogene [Source:HGNC Symbol;Acc:HGNC:47576]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479837","summary":null,"start":229894346,"end":229894453,"strand":1,"description":"RNA, U6 small nuclear 613, pseudogene [Source:HGNC Symbol;Acc:HGNC:47576]"}, {"versioned_ensembl_gene_id":"ENSG00000275822.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54835171,"end":54842110,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000222421.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127832635,"end":127832743,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200812.1","gene_symbol":"SNORD115-6","gene_name":"small nucleolar RNA, C/D box 115-6 [Source:HGNC Symbol;Acc:HGNC:33025]","synonyms":"HBII-52-6","biotype":"snoRNA","ncbi_id":"100033443","summary":null,"start":25180497,"end":25180578,"strand":1,"description":"small nucleolar RNA, C/D box 115-6 [Source:HGNC Symbol;Acc:HGNC:33025]"}, {"versioned_ensembl_gene_id":"ENSG00000276955.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28524151,"end":28524440,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207525.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74463888,"end":74463988,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207731.1","gene_symbol":"MIR506","gene_name":"microRNA 506 [Source:HGNC Symbol;Acc:HGNC:32143]","synonyms":"MIRN506,hsa-mir-506","biotype":"miRNA","ncbi_id":"574511","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147230720,"end":147230843,"strand":-1,"description":"microRNA 506 [Source:HGNC Symbol;Acc:HGNC:32143]"}, {"versioned_ensembl_gene_id":"ENSG00000239081.1","gene_symbol":"RNU7-24P","gene_name":"RNA, U7 small nuclear 24 pseudogene [Source:HGNC Symbol;Acc:HGNC:34120]","synonyms":"U7.24,RNU7P3,HSU7.25","biotype":"snRNA","ncbi_id":"6074","summary":null,"start":24400056,"end":24400117,"strand":-1,"description":"RNA, U7 small nuclear 24 pseudogene [Source:HGNC Symbol;Acc:HGNC:34120]"}, {"versioned_ensembl_gene_id":"ENSG00000275377.1","gene_symbol":"MIR1299","gene_name":"microRNA 1299 [Source:HGNC Symbol;Acc:HGNC:35290]","synonyms":"MIRN1299,hsa-mir-1299","biotype":"miRNA","ncbi_id":"100302167","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40929010,"end":40929092,"strand":-1,"description":"microRNA 1299 [Source:HGNC Symbol;Acc:HGNC:35290]"}, {"versioned_ensembl_gene_id":"ENSG00000216077.3","gene_symbol":"MIR887","gene_name":"microRNA 887 [Source:HGNC Symbol;Acc:HGNC:33661]","synonyms":"MIRN887,hsa-mir-887","biotype":"miRNA","ncbi_id":"100126347","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15935182,"end":15935260,"strand":1,"description":"microRNA 887 [Source:HGNC Symbol;Acc:HGNC:33661]"}, {"versioned_ensembl_gene_id":"ENSG00000240733.3","gene_symbol":"RN7SL502P","gene_name":"RNA, 7SL, cytoplasmic 502, pseudogene [Source:HGNC Symbol;Acc:HGNC:46518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479407","summary":null,"start":36450912,"end":36451201,"strand":-1,"description":"RNA, 7SL, cytoplasmic 502, pseudogene [Source:HGNC Symbol;Acc:HGNC:46518]"}, {"versioned_ensembl_gene_id":"ENSG00000252496.1","gene_symbol":"RNA5SP33","gene_name":"RNA, 5S ribosomal pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42609]","synonyms":"RN5S33","biotype":"rRNA","ncbi_id":"100873365","summary":null,"start":79389534,"end":79389631,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42609]"}, {"versioned_ensembl_gene_id":"ENSG00000276599.1","gene_symbol":"RNA5SP411","gene_name":"RNA, 5S ribosomal pseudogene 411 [Source:HGNC Symbol;Acc:HGNC:43311]","synonyms":"RN5S411","biotype":"rRNA","ncbi_id":"100887740","summary":null,"start":35746523,"end":35746636,"strand":1,"description":"RNA, 5S ribosomal pseudogene 411 [Source:HGNC Symbol;Acc:HGNC:43311]"}, {"versioned_ensembl_gene_id":"ENSG00000206709.1","gene_symbol":"RNU6-1080P","gene_name":"RNA, U6 small nuclear 1080, pseudogene [Source:HGNC Symbol;Acc:HGNC:48043]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481520","summary":null,"start":73339094,"end":73339200,"strand":-1,"description":"RNA, U6 small nuclear 1080, pseudogene [Source:HGNC Symbol;Acc:HGNC:48043]"}, {"versioned_ensembl_gene_id":"ENSG00000207197.1","gene_symbol":"SNORD116-12","gene_name":"small nucleolar RNA, C/D box 116-12 [Source:HGNC Symbol;Acc:HGNC:33078]","synonyms":"HBII-85-12","biotype":"snoRNA","ncbi_id":"100033424","summary":null,"start":25077051,"end":25077142,"strand":1,"description":"small nucleolar RNA, C/D box 116-12 [Source:HGNC Symbol;Acc:HGNC:33078]"}, {"versioned_ensembl_gene_id":"ENSG00000206583.1","gene_symbol":"RNU6-1292P","gene_name":"RNA, U6 small nuclear 1292, pseudogene [Source:HGNC Symbol;Acc:HGNC:48255]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480656","summary":null,"start":85509938,"end":85510044,"strand":1,"description":"RNA, U6 small nuclear 1292, pseudogene [Source:HGNC Symbol;Acc:HGNC:48255]"}, {"versioned_ensembl_gene_id":"ENSG00000206684.1","gene_symbol":"RNU6-157P","gene_name":"RNA, U6 small nuclear 157, pseudogene [Source:HGNC Symbol;Acc:HGNC:47120]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479636","summary":null,"start":172366540,"end":172366646,"strand":1,"description":"RNA, U6 small nuclear 157, pseudogene [Source:HGNC Symbol;Acc:HGNC:47120]"}, {"versioned_ensembl_gene_id":"ENSG00000251906.2","gene_symbol":"RNU6-351P","gene_name":"RNA, U6 small nuclear 351, pseudogene [Source:HGNC Symbol;Acc:HGNC:47314]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479722","summary":null,"start":104974672,"end":104974771,"strand":1,"description":"RNA, U6 small nuclear 351, pseudogene [Source:HGNC Symbol;Acc:HGNC:47314]"}, {"versioned_ensembl_gene_id":"ENSG00000207546.1","gene_symbol":"MIR548C","gene_name":"microRNA 548c [Source:HGNC Symbol;Acc:HGNC:32800]","synonyms":"MIRN548C,hsa-mir-548c","biotype":"miRNA","ncbi_id":"693129","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64622509,"end":64622605,"strand":1,"description":"microRNA 548c [Source:HGNC Symbol;Acc:HGNC:32800]"}, {"versioned_ensembl_gene_id":"ENSG00000207356.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39944890,"end":39944998,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252149.1","gene_symbol":"RNA5SP315","gene_name":"RNA, 5S ribosomal pseudogene 315 [Source:HGNC Symbol;Acc:HGNC:43215]","synonyms":"RN5S315","biotype":"rRNA","ncbi_id":"106479005","summary":null,"start":48040462,"end":48040577,"strand":1,"description":"RNA, 5S ribosomal pseudogene 315 [Source:HGNC Symbol;Acc:HGNC:43215]"}, {"versioned_ensembl_gene_id":"ENSG00000208839.1","gene_symbol":"SNORA35","gene_name":"small nucleolar RNA, H/ACA box 35 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000281269.1","gene_symbol":"AC068724.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":43109928,"end":43110018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223042.1","gene_symbol":"RN7SKP161","gene_name":"RNA, 7SK small nuclear pseudogene 161 [Source:HGNC Symbol;Acc:HGNC:45885]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479167","summary":null,"start":10084186,"end":10084490,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 161 [Source:HGNC Symbol;Acc:HGNC:45885]"}, {"versioned_ensembl_gene_id":"ENSG00000207343.1","gene_symbol":"RNU6-225P","gene_name":"RNA, U6 small nuclear 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:47188]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479667","summary":null,"start":20416797,"end":20416899,"strand":-1,"description":"RNA, U6 small nuclear 225, pseudogene [Source:HGNC Symbol;Acc:HGNC:47188]"}, {"versioned_ensembl_gene_id":"ENSG00000251807.1","gene_symbol":"RNU6-202P","gene_name":"RNA, U6 small nuclear 202, pseudogene [Source:HGNC Symbol;Acc:HGNC:47165]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479656","summary":null,"start":41919254,"end":41919349,"strand":-1,"description":"RNA, U6 small nuclear 202, pseudogene [Source:HGNC Symbol;Acc:HGNC:47165]"}, {"versioned_ensembl_gene_id":"ENSG00000238519.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30384959,"end":30385091,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000200336.1","gene_symbol":"RNA5SP333","gene_name":"RNA, 5S ribosomal pseudogene 333 [Source:HGNC Symbol;Acc:HGNC:43233]","synonyms":"RN5S333","biotype":"rRNA","ncbi_id":"106480763","summary":null,"start":18248389,"end":18248506,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 333 [Source:HGNC Symbol;Acc:HGNC:43233]"}, {"versioned_ensembl_gene_id":"ENSG00000243905.3","gene_symbol":"RN7SL679P","gene_name":"RNA, 7SL, cytoplasmic 679, pseudogene [Source:HGNC Symbol;Acc:HGNC:46695]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481855","summary":null,"start":26593243,"end":26593546,"strand":-1,"description":"RNA, 7SL, cytoplasmic 679, pseudogene [Source:HGNC Symbol;Acc:HGNC:46695]"}, {"versioned_ensembl_gene_id":"ENSG00000252450.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32286452,"end":32286561,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238575.1","gene_symbol":"snoU109","gene_name":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":2555358,"end":2555492,"strand":1,"description":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]"}, {"versioned_ensembl_gene_id":"ENSG00000200953.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51156868,"end":51156977,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201938.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96103079,"end":96103174,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284718.1","gene_symbol":"AC093762.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227728335,"end":227728625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207029.1","gene_symbol":"RNU6-43P","gene_name":"RNA, U6 small nuclear 43, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201541.1","gene_symbol":"SNORA1","gene_name":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]","synonyms":"ACA1","biotype":"snoRNA","ncbi_id":"677792","summary":null,"start":24333415,"end":24333547,"strand":-1,"description":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]"}, {"versioned_ensembl_gene_id":"ENSG00000200444.1","gene_symbol":"RNU6-1339P","gene_name":"RNA, U6 small nuclear 1339, pseudogene [Source:HGNC Symbol;Acc:HGNC:48302]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481603","summary":null,"start":83824863,"end":83824953,"strand":-1,"description":"RNA, U6 small nuclear 1339, pseudogene [Source:HGNC Symbol;Acc:HGNC:48302]"}, {"versioned_ensembl_gene_id":"ENSG00000199895.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":92170353,"end":92170453,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284518.1","gene_symbol":"MIR4658","gene_name":"microRNA 4658 [Source:HGNC Symbol;Acc:HGNC:41673]","synonyms":"hsa-mir-4658","biotype":"miRNA","ncbi_id":"100616439","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100156605,"end":100156669,"strand":-1,"description":"microRNA 4658 [Source:HGNC Symbol;Acc:HGNC:41673]"}, {"versioned_ensembl_gene_id":"ENSG00000212440.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":9286673,"end":9286822,"strand":-1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000207984.1","gene_symbol":"MIR513A2","gene_name":"microRNA 513a-2 [Source:HGNC Symbol;Acc:HGNC:32142]","synonyms":"MIRN513A2,MIRN513A-2,MIRN513-2,hsa-mir-513-2","biotype":"miRNA","ncbi_id":"574510","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147225826,"end":147225952,"strand":-1,"description":"microRNA 513a-2 [Source:HGNC Symbol;Acc:HGNC:32142]"}, {"versioned_ensembl_gene_id":"ENSG00000264675.1","gene_symbol":"MIR4285","gene_name":"microRNA 4285 [Source:HGNC Symbol;Acc:HGNC:38337]","synonyms":"hsa-mir-4285","biotype":"miRNA","ncbi_id":"100422858","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102293103,"end":102293187,"strand":1,"description":"microRNA 4285 [Source:HGNC Symbol;Acc:HGNC:38337]"}, {"versioned_ensembl_gene_id":"ENSG00000263763.1","gene_symbol":"MIR3686","gene_name":"microRNA 3686 [Source:HGNC Symbol;Acc:HGNC:38887]","synonyms":"hsa-mir-3686","biotype":"miRNA","ncbi_id":"100500839","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129484057,"end":129484142,"strand":-1,"description":"microRNA 3686 [Source:HGNC Symbol;Acc:HGNC:38887]"}, {"versioned_ensembl_gene_id":"ENSG00000207963.1","gene_symbol":"MIR569","gene_name":"microRNA 569 [Source:HGNC Symbol;Acc:HGNC:32825]","synonyms":"MIRN569,hsa-mir-569","biotype":"miRNA","ncbi_id":"693154","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":171106664,"end":171106759,"strand":-1,"description":"microRNA 569 [Source:HGNC Symbol;Acc:HGNC:32825]"}, {"versioned_ensembl_gene_id":"ENSG00000251837.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93027410,"end":93027506,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202538.1","gene_symbol":"RNU4-2","gene_name":"RNA, U4 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10193]","synonyms":"U4c,U4b,U4A,RNU4C,RNU4B1,RNU4-1B","biotype":"snRNA","ncbi_id":"26834","summary":null,"start":120291763,"end":120291903,"strand":-1,"description":"RNA, U4 small nuclear 2 [Source:HGNC Symbol;Acc:HGNC:10193]"}, {"versioned_ensembl_gene_id":"ENSG00000275161.1","gene_symbol":"Mico1","gene_name":"Maternal intergenic circadian oscillating RNA 1 [Source:RFAM;Acc:RF01928]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100816041,"end":100816244,"strand":1,"description":"Maternal intergenic circadian oscillating RNA 1 [Source:RFAM;Acc:RF01928]"}, {"versioned_ensembl_gene_id":"ENSG00000199833.1","gene_symbol":"SNORD115-21","gene_name":"small nucleolar RNA, C/D box 115-21 [Source:HGNC Symbol;Acc:HGNC:33040]","synonyms":"HBII-52-21","biotype":"snoRNA","ncbi_id":"100033603","summary":null,"start":25208083,"end":25208163,"strand":1,"description":"small nucleolar RNA, C/D box 115-21 [Source:HGNC Symbol;Acc:HGNC:33040]"}, {"versioned_ensembl_gene_id":"ENSG00000277635.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":109295239,"end":109295498,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212610.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":218541690,"end":218541899,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000284027.1","gene_symbol":"MIR497","gene_name":"microRNA 497 [Source:HGNC Symbol;Acc:HGNC:32088]","synonyms":"MIRN497,hsa-mir-497","biotype":"miRNA","ncbi_id":"574456","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7017911,"end":7018022,"strand":-1,"description":"microRNA 497 [Source:HGNC Symbol;Acc:HGNC:32088]"}, {"versioned_ensembl_gene_id":"ENSG00000207368.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":195419436,"end":195419546,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200537.1","gene_symbol":"RNY4P6","gene_name":"RNA, Ro-associated Y4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34055]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379287","summary":null,"start":117015897,"end":117015992,"strand":1,"description":"RNA, Ro-associated Y4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34055]"}, {"versioned_ensembl_gene_id":"ENSG00000284525.1","gene_symbol":"MIR4687","gene_name":"microRNA 4687 [Source:HGNC Symbol;Acc:HGNC:41712]","synonyms":"hsa-mir-4687","biotype":"miRNA","ncbi_id":"100616453","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3856062,"end":3856141,"strand":1,"description":"microRNA 4687 [Source:HGNC Symbol;Acc:HGNC:41712]"}, {"versioned_ensembl_gene_id":"ENSG00000222721.1","gene_symbol":"RN7SKP188","gene_name":"RNA, 7SK small nuclear pseudogene 188 [Source:HGNC Symbol;Acc:HGNC:45912]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479179","summary":null,"start":167662986,"end":167663302,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 188 [Source:HGNC Symbol;Acc:HGNC:45912]"}, {"versioned_ensembl_gene_id":"ENSG00000207229.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55040847,"end":55040945,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283678.1","gene_symbol":"MIR6830","gene_name":"microRNA 6830 [Source:HGNC Symbol;Acc:HGNC:49966]","synonyms":"hsa-mir-6830","biotype":"miRNA","ncbi_id":"102465498","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":132217849,"end":132217918,"strand":-1,"description":"microRNA 6830 [Source:HGNC Symbol;Acc:HGNC:49966]"}, {"versioned_ensembl_gene_id":"ENSG00000222302.1","gene_symbol":"RNA5SP371","gene_name":"RNA, 5S ribosomal pseudogene 371 [Source:HGNC Symbol;Acc:HGNC:43271]","synonyms":"RN5S371","biotype":"rRNA","ncbi_id":"100873629","summary":null,"start":107486511,"end":107486635,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 371 [Source:HGNC Symbol;Acc:HGNC:43271]"}, {"versioned_ensembl_gene_id":"ENSG00000223023.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23024596,"end":23024703,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252112.1","gene_symbol":"SNORD63","gene_name":"Small nucleolar RNA SNORD63 [Source:RFAM;Acc:RF00154]","synonyms":"U63,SNORD63A,RNU63","biotype":"snoRNA","ncbi_id":"26785","summary":null,"start":30246757,"end":30246820,"strand":-1,"description":"Small nucleolar RNA SNORD63 [Source:RFAM;Acc:RF00154]"}, {"versioned_ensembl_gene_id":"ENSG00000199407.1","gene_symbol":"RNA5SP301","gene_name":"RNA, 5S ribosomal pseudogene 301 [Source:HGNC Symbol;Acc:HGNC:43201]","synonyms":"RN5S301","biotype":"rRNA","ncbi_id":"100873576","summary":null,"start":13727796,"end":13727916,"strand":1,"description":"RNA, 5S ribosomal pseudogene 301 [Source:HGNC Symbol;Acc:HGNC:43201]"}, {"versioned_ensembl_gene_id":"ENSG00000247372.2","gene_symbol":"AC008897.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75320155,"end":75336914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229814.1","gene_symbol":"RPL35AP21","gene_name":"ribosomal protein L35a pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36814]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271506","summary":null,"start":71589601,"end":71589933,"strand":1,"description":"ribosomal protein L35a pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36814]"}, {"versioned_ensembl_gene_id":"ENSG00000196390.6","gene_symbol":"AC116337.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74929880,"end":74930566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163481.7","gene_symbol":"RNF25","gene_name":"ring finger protein 25 [Source:HGNC Symbol;Acc:HGNC:14662]","synonyms":"FLJ13906,AO7","biotype":"protein_coding","ncbi_id":"64320","summary":"The protein encoded by this gene contains a RING finger motif. The mouse counterpart of this protein has been shown to interact with Rela, the p65 subunit of NF-kappaB (NFKB), and modulate NFKB-mediated transcription activity. The mouse protein also binds ubiquitin-conjugating enzymes (E2s) and is a substrate for E2-dependent ubiquitination. [provided by RefSeq, Jul 2008]","start":218663864,"end":218672411,"strand":-1,"description":"ring finger protein 25 [Source:HGNC Symbol;Acc:HGNC:14662]"}, {"versioned_ensembl_gene_id":"ENSG00000228417.1","gene_symbol":"AL360182.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110207850,"end":110208591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214067.2","gene_symbol":"AL360182.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110257064,"end":110257843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264930.1","gene_symbol":"AC131055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22606388,"end":22606703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261020.1","gene_symbol":"AC132825.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22420022,"end":22424731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164758.7","gene_symbol":"MED30","gene_name":"mediator complex subunit 30 [Source:HGNC Symbol;Acc:HGNC:23032]","synonyms":"TRAP25,THRAP6","biotype":"protein_coding","ncbi_id":"90390","summary":"The multiprotein TRAP/Mediator complex facilitates gene expression through a wide variety of transcriptional activators. MED30 is a component of this complex that appears to be metazoan specific (Baek et al., 2002 [PubMed 11909976]).[supplied by OMIM, Nov 2010]","start":117520713,"end":117540262,"strand":1,"description":"mediator complex subunit 30 [Source:HGNC Symbol;Acc:HGNC:23032]"}, {"versioned_ensembl_gene_id":"ENSG00000271757.1","gene_symbol":"AP002360.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76392196,"end":76392905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164346.9","gene_symbol":"NSA2","gene_name":"NSA2, ribosome biogenesis homolog [Source:HGNC Symbol;Acc:HGNC:30728]","synonyms":"TINP1,HUSSY-29,HCLG1,FLJ94393","biotype":"protein_coding","ncbi_id":"10412","summary":"This gene encodes a nucleolar protein involved in cell cycle regulation and proliferation. This gene was identified based on sequence similarity to a highly conserved Saccharomyces cerevisiae gene encoding a pre-ribosomal protein, which is involved in large ribosomal subunit biogenesis. The encoded protein is found at elevated levels in diabetic nephropathy. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified. [provided by RefSeq, Nov 2012]","start":74766991,"end":74780113,"strand":1,"description":"NSA2, ribosome biogenesis homolog [Source:HGNC Symbol;Acc:HGNC:30728]"}, {"versioned_ensembl_gene_id":"ENSG00000174567.7","gene_symbol":"GOLT1A","gene_name":"golgi transport 1A [Source:HGNC Symbol;Acc:HGNC:24766]","synonyms":"MGC62027,GOT1,FLJ42654,CGI-141,YMR292W","biotype":"protein_coding","ncbi_id":"127845","summary":null,"start":204198160,"end":204214092,"strand":-1,"description":"golgi transport 1A [Source:HGNC Symbol;Acc:HGNC:24766]"}, {"versioned_ensembl_gene_id":"ENSG00000143839.14","gene_symbol":"REN","gene_name":"renin [Source:HGNC Symbol;Acc:HGNC:9958]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5972","summary":"This gene encodes renin, an aspartic protease that is secreted by the kidneys. Renin is a part of the renin-angiotensin-aldosterone system involved in regulation of blood pressure, and electrolyte balance. This enzyme catalyzes the first step in the activation pathway of angiotensinogen by cleaving angiotensinogen to form angiotensin I, which is then converted to angiotensin II by angiotensin I converting enzyme. This cascade can result in aldosterone release, narrowing of blood vessels, and increase in blood pressure as angiotension II is a vasoconstrictive peptide. Transcript variants that encode different protein isoforms and that arise from alternative splicing and the use of alternative promoters have been described, but their full-length nature has not been determined. Mutations in this gene have been shown to cause hyperuricemic nephropathy familial juvenile 2, familial hyperproreninemia, and renal tubular dysgenesis. [provided by RefSeq, May 2020]","start":204154819,"end":204190324,"strand":-1,"description":"renin [Source:HGNC Symbol;Acc:HGNC:9958]"}, {"versioned_ensembl_gene_id":"ENSG00000034152.18","gene_symbol":"MAP2K3","gene_name":"mitogen-activated protein kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6843]","synonyms":"PRKMK3,MKK3,MEK3,MAPKK3","biotype":"protein_coding","ncbi_id":"5606","summary":"The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase is activated by mitogenic and environmental stress, and participates in the MAP kinase-mediated signaling cascade. It phosphorylates and thus activates MAPK14/p38-MAPK. This kinase can be activated by insulin, and is necessary for the expression of glucose transporter. Expression of RAS oncogene is found to result in the accumulation of the active form of this kinase, which thus leads to the constitutive activation of MAPK14, and confers oncogenic transformation of primary cells. The inhibition of this kinase is involved in the pathogenesis of Yersina pseudotuberculosis. Multiple alternatively spliced transcript variants that encode distinct isoforms have been reported for this gene. [provided by RefSeq, Jul 2008]","start":21284672,"end":21315240,"strand":1,"description":"mitogen-activated protein kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6843]"}, {"versioned_ensembl_gene_id":"ENSG00000258904.1","gene_symbol":"AL157871.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":100263781,"end":100265405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122218.14","gene_symbol":"COPA","gene_name":"coatomer protein complex subunit alpha [Source:HGNC Symbol;Acc:HGNC:2230]","synonyms":"HEP-COP","biotype":"protein_coding","ncbi_id":"1314","summary":"In eukaryotic cells, protein transport between the endoplasmic reticulum and Golgi compartments is mediated in part by non-clathrin-coated vesicular coat proteins (COPs). Seven coat proteins have been identified, and they represent subunits of a complex known as coatomer. The subunits are designated alpha-COP, beta-COP, beta-prime-COP, gamma-COP, delta-COP, epsilon-COP, and zeta-COP. The alpha-COP, encoded by COPA, shares high sequence similarity with RET1P, the alpha subunit of the coatomer complex in yeast. Also, the N-terminal 25 amino acids of alpha-COP encode the bioactive peptide, xenin, which stimulates exocrine pancreatic secretion and may act as a gastrointestinal hormone. Alternative splicing results in multiple splice forms encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":160289273,"end":160343400,"strand":-1,"description":"coatomer protein complex subunit alpha [Source:HGNC Symbol;Acc:HGNC:2230]"}, {"versioned_ensembl_gene_id":"ENSG00000248677.1","gene_symbol":"LINC02102","gene_name":"long intergenic non-protein coding RNA 2102 [Source:HGNC Symbol;Acc:HGNC:52957]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505625","summary":null,"start":6686325,"end":6707711,"strand":-1,"description":"long intergenic non-protein coding RNA 2102 [Source:HGNC Symbol;Acc:HGNC:52957]"}, {"versioned_ensembl_gene_id":"ENSG00000159708.17","gene_symbol":"LRRC36","gene_name":"leucine rich repeat containing 36 [Source:HGNC Symbol;Acc:HGNC:25615]","synonyms":"FLJ11004","biotype":"protein_coding","ncbi_id":"55282","summary":null,"start":67326798,"end":67385203,"strand":1,"description":"leucine rich repeat containing 36 [Source:HGNC Symbol;Acc:HGNC:25615]"}, {"versioned_ensembl_gene_id":"ENSG00000279817.1","gene_symbol":"AC073911.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133077762,"end":133078392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265688.1","gene_symbol":"MAFG-AS1","gene_name":"MAFG antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43649]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"92659","summary":null,"start":81927829,"end":81930753,"strand":1,"description":"MAFG antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43649]"}, {"versioned_ensembl_gene_id":"ENSG00000268636.1","gene_symbol":"AC011495.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49625994,"end":49626439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223701.3","gene_symbol":"RAET1E-AS1","gene_name":"RAET1E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48994]","synonyms":"RAET1G-AS1,RAET1G-AS1","biotype":"antisense_RNA","ncbi_id":"100652739","summary":null,"start":149884431,"end":149919508,"strand":1,"description":"RAET1E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48994]"}, {"versioned_ensembl_gene_id":"ENSG00000132000.11","gene_symbol":"PODNL1","gene_name":"podocan like 1 [Source:HGNC Symbol;Acc:HGNC:26275]","synonyms":"SLRR5B,FLJ23447","biotype":"protein_coding","ncbi_id":"79883","summary":null,"start":13931187,"end":13953392,"strand":-1,"description":"podocan like 1 [Source:HGNC Symbol;Acc:HGNC:26275]"}, {"versioned_ensembl_gene_id":"ENSG00000254854.1","gene_symbol":"AP003390.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119729583,"end":119739623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254099.1","gene_symbol":"AC005740.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141970637,"end":141982687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248954.1","gene_symbol":"AC027801.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49887598,"end":49900893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106723.16","gene_symbol":"SPIN1","gene_name":"spindlin 1 [Source:HGNC Symbol;Acc:HGNC:11243]","synonyms":"TDRD24,SPIN","biotype":"protein_coding","ncbi_id":"10927","summary":null,"start":88388419,"end":88478694,"strand":1,"description":"spindlin 1 [Source:HGNC Symbol;Acc:HGNC:11243]"}, {"versioned_ensembl_gene_id":"ENSG00000267123.5","gene_symbol":"LINC02081","gene_name":"long intergenic non-protein coding RNA 2081 [Source:HGNC Symbol;Acc:HGNC:52930]","synonyms":"XLOC_012582,CTD-2357A8.3","biotype":"lincRNA","ncbi_id":"101928710","summary":null,"start":78617389,"end":78632057,"strand":-1,"description":"long intergenic non-protein coding RNA 2081 [Source:HGNC Symbol;Acc:HGNC:52930]"}, {"versioned_ensembl_gene_id":"ENSG00000213209.2","gene_symbol":"AC005229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148637179,"end":148637587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213210.4","gene_symbol":"AC005229.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148580401,"end":148580799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283504.1","gene_symbol":"AC006974.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148473599,"end":148503458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255247.1","gene_symbol":"AP003390.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119709920,"end":119713925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224048.5","gene_symbol":"AC104777.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150612381,"end":150635348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161653.10","gene_symbol":"NAGS","gene_name":"N-acetylglutamate synthase [Source:HGNC Symbol;Acc:HGNC:17996]","synonyms":"NAT7,ARGA,AGAS","biotype":"protein_coding","ncbi_id":"162417","summary":"The N-acetylglutamate synthase gene encodes a mitochondrial enzyme that catalyzes the formation of N-acetylglutamate (NAG) from glutamate and acetyl coenzyme-A. NAG is a cofactor of carbamyl phosphate synthetase I (CPSI), the first enzyme of the urea cycle in mammals. This gene may regulate ureagenesis by altering NAG availability and, thereby, CPSI activity. Deficiencies in N-acetylglutamate synthase have been associated with hyperammonemia. [provided by RefSeq, Jul 2008]","start":44004546,"end":44009063,"strand":1,"description":"N-acetylglutamate synthase [Source:HGNC Symbol;Acc:HGNC:17996]"}, {"versioned_ensembl_gene_id":"ENSG00000232359.1","gene_symbol":"AC104777.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150595102,"end":150620067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274133.1","gene_symbol":"AC083849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148445786,"end":148446299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131096.10","gene_symbol":"PYY","gene_name":"peptide YY [Source:HGNC Symbol;Acc:HGNC:9748]","synonyms":"PYY1","biotype":"protein_coding","ncbi_id":"5697","summary":"This gene encodes a member of the neuropeptide Y (NPY) family of peptides. The encoded preproprotein is proteolytically processed to generate two alternative peptide products that differ in length by three amino acids. These peptides, secreted by endocrine cells in the gut, exhibit different binding affinities for each of the neuropeptide Y receptors. Binding of the encoded peptides to these receptors mediates regulation of pancreatic secretion, gut mobility and energy homeostasis. Rare variations in this gene could increase susceptibility to obesity and elevated serum levels of the encoded peptides may be associated with anorexia nervosa. [provided by RefSeq, Feb 2016]","start":43952738,"end":44004469,"strand":-1,"description":"peptide YY [Source:HGNC Symbol;Acc:HGNC:9748]"}, {"versioned_ensembl_gene_id":"ENSG00000133943.20","gene_symbol":"C14orf159","gene_name":"chromosome 14 open reading frame 159 [Source:HGNC Symbol;Acc:HGNC:20498]","synonyms":"FLJ39975","biotype":"protein_coding","ncbi_id":"80017","summary":null,"start":91060333,"end":91225632,"strand":1,"description":"chromosome 14 open reading frame 159 [Source:HGNC Symbol;Acc:HGNC:20498]"}, {"versioned_ensembl_gene_id":"ENSG00000272255.1","gene_symbol":"AC113361.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139644460,"end":139645002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267770.1","gene_symbol":"AC016182.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78522247,"end":78522828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110400.10","gene_symbol":"NECTIN1","gene_name":"nectin cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:9706]","synonyms":"PRR1,PRR,OFC7,HVEC,HIgR,ED4,CLPED1,CD111,SK-12,PVRR1,PVRL1","biotype":"protein_coding","ncbi_id":"5818","summary":"This gene encodes an adhesion protein that plays a role in the organization of adherens junctions and tight junctions in epithelial and endothelial cells. The protein is a calcium(2+)-independent cell-cell adhesion molecule that belongs to the immunoglobulin superfamily and has 3 extracellular immunoglobulin-like loops, a single transmembrane domain (in some isoforms), and a cytoplasmic region. This protein acts as a receptor for glycoprotein D (gD) of herpes simplex viruses 1 and 2 (HSV-1, HSV-2), and pseudorabies virus (PRV) and mediates viral entry into epithelial and neuronal cells. Mutations in this gene cause cleft lip and palate/ectodermal dysplasia 1 syndrome (CLPED1) as well as non-syndromic cleft lip with or without cleft palate (CL/P). Alternative splicing results in multiple transcript variants encoding proteins with distinct C-termini. [provided by RefSeq, Oct 2009]","start":119623408,"end":119729084,"strand":-1,"description":"nectin cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:9706]"}, {"versioned_ensembl_gene_id":"ENSG00000261949.5","gene_symbol":"GFY","gene_name":"golgi associated olfactory signaling regulator [Source:HGNC Symbol;Acc:HGNC:44663]","synonyms":"Goofy","biotype":"protein_coding","ncbi_id":"100507003","summary":null,"start":49423749,"end":49428818,"strand":1,"description":"golgi associated olfactory signaling regulator [Source:HGNC Symbol;Acc:HGNC:44663]"}, {"versioned_ensembl_gene_id":"ENSG00000142538.1","gene_symbol":"PTH2","gene_name":"parathyroid hormone 2 [Source:HGNC Symbol;Acc:HGNC:30828]","synonyms":"TIP39","biotype":"protein_coding","ncbi_id":"113091","summary":"This gene encodes the precursor of a peptide hormone that shares sequence similarity with the parathyroid hormone. This gene is expressed in various regions of the brain where it plays a role in the release of pituitary hormones, anxiety and nociception. The encoded precursor protein is proteolytically processed to generate the biologically active neuropeptide. [provided by RefSeq, Jul 2015]","start":49422414,"end":49423441,"strand":-1,"description":"parathyroid hormone 2 [Source:HGNC Symbol;Acc:HGNC:30828]"}, {"versioned_ensembl_gene_id":"ENSG00000123684.12","gene_symbol":"LPGAT1","gene_name":"lysophosphatidylglycerol acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:28985]","synonyms":"NET8,KIAA0205,FAM34A1,FAM34A","biotype":"protein_coding","ncbi_id":"9926","summary":"This gene encodes a member of the lysophospholipid acyltransferase family. The encoded protein catalyzes the reacylation of lysophosphatidylglycerol to phosphatidylglycerol, a membrane phospholipid that is an important precursor for the synthesis of cardiolipin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":211743457,"end":211830772,"strand":-1,"description":"lysophosphatidylglycerol acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:28985]"}, {"versioned_ensembl_gene_id":"ENSG00000224896.2","gene_symbol":"SIGLEC30P","gene_name":"sialic acid binding Ig like lectin 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:15623]","synonyms":"SIGLECP14","biotype":"processed_pseudogene","ncbi_id":"114190","summary":null,"start":170115636,"end":170116576,"strand":1,"description":"sialic acid binding Ig like lectin 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:15623]"}, {"versioned_ensembl_gene_id":"ENSG00000170906.15","gene_symbol":"NDUFA3","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 [Source:HGNC Symbol;Acc:HGNC:7686]","synonyms":"B9","biotype":"protein_coding","ncbi_id":"4696","summary":null,"start":54102728,"end":54109257,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 [Source:HGNC Symbol;Acc:HGNC:7686]"}, {"versioned_ensembl_gene_id":"ENSG00000235538.1","gene_symbol":"AL137005.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163703904,"end":163759841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250390.2","gene_symbol":"AP001790.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95482406,"end":95497553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235137.2","gene_symbol":"HSP90AB6P","gene_name":"heat shock protein 90 alpha family class B member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"541611","summary":null,"start":96883842,"end":96885821,"strand":-1,"description":"heat shock protein 90 alpha family class B member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32540]"}, {"versioned_ensembl_gene_id":"ENSG00000236426.5","gene_symbol":"AL583824.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119330233,"end":119336182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177688.6","gene_symbol":"SUMO4","gene_name":"small ubiquitin-like modifier 4 [Source:HGNC Symbol;Acc:HGNC:21181]","synonyms":"SMT3H4,IDDM5,dJ281H8.4","biotype":"protein_coding","ncbi_id":"387082","summary":"This gene is a member of the SUMO gene family. This family of genes encode small ubiquitin-related modifiers that are attached to proteins and control the target proteins' subcellular localization, stability, or activity. The protein described in this record is located in the cytoplasm and specifically modifies IKBA, leading to negative regulation of NF-kappa-B-dependent transcription of the IL12B gene. A specific polymorphism in this SUMO gene, which leads to the M55V substitution, has been associated with type I diabetes. The RefSeq contains this polymorphism. [provided by RefSeq, Jul 2008]","start":149400227,"end":149401292,"strand":1,"description":"small ubiquitin-like modifier 4 [Source:HGNC Symbol;Acc:HGNC:21181]"}, {"versioned_ensembl_gene_id":"ENSG00000213892.11","gene_symbol":"CEACAM16","gene_name":"carcinoembryonic antigen related cell adhesion molecule 16 [Source:HGNC Symbol;Acc:HGNC:31948]","synonyms":"DFNA4B","biotype":"protein_coding","ncbi_id":"388551","summary":"The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012]","start":44699151,"end":44710714,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 16 [Source:HGNC Symbol;Acc:HGNC:31948]"}, {"versioned_ensembl_gene_id":"ENSG00000140057.8","gene_symbol":"AK7","gene_name":"adenylate kinase 7 [Source:HGNC Symbol;Acc:HGNC:20091]","synonyms":"FLJ32864","biotype":"protein_coding","ncbi_id":"122481","summary":"This gene encodes a member of the adenylate kinase family of enzymes. The encoded enzyme is a phosphotransferase that catalyzes the reversible phosphorylation of adenine nucleotides. This enzyme plays a role in energy homeostasis of the cell. Alternative splicing results in multiple transcript variants. Mutations in the mouse gene are associated with primary ciliary dyskinesia. [provided by RefSeq, Apr 2017]","start":96392111,"end":96489427,"strand":1,"description":"adenylate kinase 7 [Source:HGNC Symbol;Acc:HGNC:20091]"}, {"versioned_ensembl_gene_id":"ENSG00000227764.1","gene_symbol":"LINC01693","gene_name":"long intergenic non-protein coding RNA 1693 [Source:HGNC Symbol;Acc:HGNC:52478]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105748977","summary":null,"start":211639695,"end":211654581,"strand":1,"description":"long intergenic non-protein coding RNA 1693 [Source:HGNC Symbol;Acc:HGNC:52478]"}, {"versioned_ensembl_gene_id":"ENSG00000279801.1","gene_symbol":"AC111170.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77444704,"end":77447167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271492.1","gene_symbol":"MEMO1P5","gene_name":"mediator of cell motility 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49102]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481668","summary":null,"start":95394049,"end":95394454,"strand":1,"description":"mediator of cell motility 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49102]"}, {"versioned_ensembl_gene_id":"ENSG00000243730.2","gene_symbol":"AL079303.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36577543,"end":36578005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136810.12","gene_symbol":"TXN","gene_name":"thioredoxin [Source:HGNC Symbol;Acc:HGNC:12435]","synonyms":"TRX","biotype":"protein_coding","ncbi_id":"7295","summary":"The protein encoded by this gene acts as a homodimer and is involved in many redox reactions. The encoded protein is active in the reversible S-nitrosylation of cysteines in certain proteins, which is part of the response to intracellular nitric oxide. This protein is found in the cytoplasm. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":110243811,"end":110256640,"strand":-1,"description":"thioredoxin [Source:HGNC Symbol;Acc:HGNC:12435]"}, {"versioned_ensembl_gene_id":"ENSG00000282834.1","gene_symbol":"AP000787.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95203727,"end":95204033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053108.16","gene_symbol":"FSTL4","gene_name":"follistatin like 4 [Source:HGNC Symbol;Acc:HGNC:21389]","synonyms":"KIAA1061","biotype":"protein_coding","ncbi_id":"23105","summary":null,"start":133196455,"end":133612564,"strand":-1,"description":"follistatin like 4 [Source:HGNC Symbol;Acc:HGNC:21389]"}, {"versioned_ensembl_gene_id":"ENSG00000232031.1","gene_symbol":"AL078599.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":81724722,"end":81736353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226977.1","gene_symbol":"HMGN1P24","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874462","summary":null,"start":95809310,"end":95809607,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39368]"}, {"versioned_ensembl_gene_id":"ENSG00000170276.5","gene_symbol":"HSPB2","gene_name":"heat shock protein family B (small) member 2 [Source:HGNC Symbol;Acc:HGNC:5247]","synonyms":"MKBP,Hs.78846","biotype":"protein_coding","ncbi_id":"3316","summary":"The protein encoded by this gene belongs to the superfamily of small heat-shock proteins containing a conservative alpha-crystallin domain at the C-terminal part of the molecule. The protein is expressed preferentially in the heart and skeletal muscle. This protein regulates Myotonic Dystrophy Protein Kinase, which plays an important role in maintenance of muscle structure and function. [provided by RefSeq, Dec 2012]","start":111912242,"end":111914093,"strand":1,"description":"heat shock protein family B (small) member 2 [Source:HGNC Symbol;Acc:HGNC:5247]"}, {"versioned_ensembl_gene_id":"ENSG00000249326.1","gene_symbol":"CTD-2194D22.4","gene_name":"uncharacterized LOC101929081 [Source:NCBI gene;Acc:101929081]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929081","summary":null,"start":1887332,"end":1900493,"strand":1,"description":"uncharacterized LOC101929081 [Source:NCBI gene;Acc:101929081]"}, {"versioned_ensembl_gene_id":"ENSG00000233967.6","gene_symbol":"AL359715.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80443344,"end":80465927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272748.1","gene_symbol":"AC063962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74821610,"end":74822130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249751.3","gene_symbol":"ECSCR","gene_name":"endothelial cell surface expressed chemotaxis and apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:35454]","synonyms":"ECSM2,ARIA","biotype":"protein_coding","ncbi_id":"641700","summary":"The protein encoded by this gene is primarily found in endothelial cells and blood vessels, where it is involved in cell shape changes and EGF-induced cell migration. It can enhance the activation of vascular endothelial growth factor receptor-2/kinase insert domain receptor and also promote the proteolysis of internalized kinase insert domain receptor. This gene may play a role in angiogenesis-related diseases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":139448556,"end":139462743,"strand":-1,"description":"endothelial cell surface expressed chemotaxis and apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:35454]"}, {"versioned_ensembl_gene_id":"ENSG00000239510.2","gene_symbol":"AL135752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58564146,"end":58564616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229300.9","gene_symbol":"C6orf48","gene_name":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]","synonyms":"G8,D6S57","biotype":"protein_coding","ncbi_id":"50854","summary":null,"start":31816794,"end":31821951,"strand":1,"description":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]"}, {"versioned_ensembl_gene_id":"ENSG00000261723.1","gene_symbol":"AC008870.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23605841,"end":23624107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157350.12","gene_symbol":"ST3GAL2","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10863]","synonyms":"ST3GALII,ST3GalA.2,SIAT4B","biotype":"protein_coding","ncbi_id":"6483","summary":"The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi but can be proteolytically processed to a soluble form. This protein, which is a member of glycosyltransferase family 29, can use the same acceptor substrates as does sialyltransferase 4A. [provided by RefSeq, Jul 2008]","start":70375978,"end":70439237,"strand":-1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10863]"}, {"versioned_ensembl_gene_id":"ENSG00000218870.1","gene_symbol":"SLC25A6P6","gene_name":"solute carrier family 25 member 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128312","summary":null,"start":70663502,"end":70664279,"strand":-1,"description":"solute carrier family 25 member 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43855]"}, {"versioned_ensembl_gene_id":"ENSG00000281219.2","gene_symbol":"LINC00254","gene_name":"long intergenic non-protein coding RNA 254 [Source:NCBI gene;Acc:64735]","synonyms":"NCRNA00254,C16orf32","biotype":"lincRNA","ncbi_id":"64735","summary":null,"start":1878285,"end":1884233,"strand":-1,"description":"long intergenic non-protein coding RNA 254 [Source:NCBI gene;Acc:64735]"}, {"versioned_ensembl_gene_id":"ENSG00000167889.12","gene_symbol":"MGAT5B","gene_name":"mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:24140]","synonyms":"GnT-VB,GnT-IX,FLJ25132","biotype":"protein_coding","ncbi_id":"146664","summary":"The MGAT5B gene encodes a beta-1,6-N-acetylglucosaminyltransferase (EC 2.4.1.155) that functions in the synthesis of complex cell surface N-glycans (Kaneko et al., 2003 [PubMed 14623122]).[supplied by OMIM, Nov 2008]","start":76868456,"end":76950393,"strand":1,"description":"mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:24140]"}, {"versioned_ensembl_gene_id":"ENSG00000167384.10","gene_symbol":"ZNF180","gene_name":"zinc finger protein 180 [Source:HGNC Symbol;Acc:HGNC:12970]","synonyms":"HHZ168","biotype":"protein_coding","ncbi_id":"7733","summary":"Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002]","start":44474428,"end":44500524,"strand":-1,"description":"zinc finger protein 180 [Source:HGNC Symbol;Acc:HGNC:12970]"}, {"versioned_ensembl_gene_id":"ENSG00000267345.1","gene_symbol":"AC010632.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37075113,"end":37078605,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255561.6","gene_symbol":"FDXACB1","gene_name":"ferredoxin-fold anticodon binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25110]","synonyms":"LOC91893,hCG_2033039","biotype":"protein_coding","ncbi_id":"91893","summary":"This gene encodes a protein which contains a ferredoxin-fold anticodon-binding domain which is contained in a subset of phenylalanyl tRNA synthetases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":111874056,"end":111881243,"strand":-1,"description":"ferredoxin-fold anticodon binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25110]"}, {"versioned_ensembl_gene_id":"ENSG00000092931.11","gene_symbol":"MFSD11","gene_name":"major facilitator superfamily domain containing 11 [Source:HGNC Symbol;Acc:HGNC:25458]","synonyms":"FLJ22196,FLJ20226","biotype":"protein_coding","ncbi_id":"79157","summary":null,"start":76735865,"end":76781449,"strand":1,"description":"major facilitator superfamily domain containing 11 [Source:HGNC Symbol;Acc:HGNC:25458]"}, {"versioned_ensembl_gene_id":"ENSG00000283629.1","gene_symbol":"AC016526.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76131707,"end":76152627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242814.2","gene_symbol":"AC113398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124808828,"end":124809233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271343.1","gene_symbol":"AL355598.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119093140,"end":119093341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253674.1","gene_symbol":"IGHVII-78-1","gene_name":"immunoglobulin heavy variable (II)-78-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5691]","synonyms":"IGHV(II)-78-1","biotype":"IG_V_pseudogene","ncbi_id":"28356","summary":null,"start":106865627,"end":106865895,"strand":-1,"description":"immunoglobulin heavy variable (II)-78-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5691]"}, {"versioned_ensembl_gene_id":"ENSG00000258791.7","gene_symbol":"LINC00520","gene_name":"long intergenic non-protein coding RNA 520 [Source:HGNC Symbol;Acc:HGNC:19843]","synonyms":"C14orf34","biotype":"lincRNA","ncbi_id":"645687","summary":null,"start":55781135,"end":55796688,"strand":-1,"description":"long intergenic non-protein coding RNA 520 [Source:HGNC Symbol;Acc:HGNC:19843]"}, {"versioned_ensembl_gene_id":"ENSG00000197813.5","gene_symbol":"AC011450.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49331617,"end":49340303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265484.1","gene_symbol":"AC091691.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71216704,"end":71237102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228730.1","gene_symbol":"LINC02013","gene_name":"long intergenic non-protein coding RNA 2013 [Source:HGNC Symbol;Acc:HGNC:52848]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374272","summary":null,"start":190697923,"end":190698848,"strand":-1,"description":"long intergenic non-protein coding RNA 2013 [Source:HGNC Symbol;Acc:HGNC:52848]"}, {"versioned_ensembl_gene_id":"ENSG00000103249.17","gene_symbol":"CLCN7","gene_name":"chloride voltage-gated channel 7 [Source:HGNC Symbol;Acc:HGNC:2025]","synonyms":"PPP1R63,OPTA2,CLC7,CLC-7","biotype":"protein_coding","ncbi_id":"1186","summary":"The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008]","start":1444934,"end":1475580,"strand":-1,"description":"chloride voltage-gated channel 7 [Source:HGNC Symbol;Acc:HGNC:2025]"}, {"versioned_ensembl_gene_id":"ENSG00000269911.1","gene_symbol":"FAM226B","gene_name":"family with sequence similarity 226 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31964]","synonyms":"CXorf50B,NCRNA00246B,LINC00246B","biotype":"sense_intronic","ncbi_id":"653687","summary":null,"start":72777608,"end":72779097,"strand":1,"description":"family with sequence similarity 226 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31964]"}, {"versioned_ensembl_gene_id":"ENSG00000266304.1","gene_symbol":"LIVAR","gene_name":"liver cell viability associated lncRNA [Source:HGNC Symbol;Acc:HGNC:53130]","synonyms":"lnc18q22.2","biotype":"lincRNA","ncbi_id":"102724895","summary":null,"start":70335929,"end":70337310,"strand":-1,"description":"liver cell viability associated lncRNA [Source:HGNC Symbol;Acc:HGNC:53130]"}, {"versioned_ensembl_gene_id":"ENSG00000253807.5","gene_symbol":"LINC01170","gene_name":"long intergenic non-protein coding RNA 1170 [Source:HGNC Symbol;Acc:HGNC:49542]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103724389","summary":null,"start":124059794,"end":124405079,"strand":-1,"description":"long intergenic non-protein coding RNA 1170 [Source:HGNC Symbol;Acc:HGNC:49542]"}, {"versioned_ensembl_gene_id":"ENSG00000109991.8","gene_symbol":"P2RX3","gene_name":"purinergic receptor P2X 3 [Source:HGNC Symbol;Acc:HGNC:8534]","synonyms":"P2X3","biotype":"protein_coding","ncbi_id":"5024","summary":"This gene encodes a member of the P2X purinergic receptor (purinoceptor) gene family which includes seven members (P2RX1 - P2RX7). P2X purinoceptors are a family of cation-permeable, ligand-gated ion channels that open in response to the binding of extracellular adenosine 5'-triphosphate (ATP). The encoded protein is a subunit of the trimeric P2X3 receptor ion channel which is expressed by sensory or autonomic neurons. A deficiency of the orthologous protein in mice is associated with reduced pain-related behavior and urinary bladder hyporeflexia. [provided by RefSeq, Aug 2017]","start":57338374,"end":57370600,"strand":1,"description":"purinergic receptor P2X 3 [Source:HGNC Symbol;Acc:HGNC:8534]"}, {"versioned_ensembl_gene_id":"ENSG00000246859.2","gene_symbol":"STARD4-AS1","gene_name":"STARD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44117]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505678","summary":null,"start":111512226,"end":111739726,"strand":1,"description":"STARD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44117]"}, {"versioned_ensembl_gene_id":"ENSG00000108107.14","gene_symbol":"RPL28","gene_name":"ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:10330]","synonyms":"L28,FLJ43307","biotype":"protein_coding","ncbi_id":"6158","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L28E family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]","start":55385345,"end":55403250,"strand":1,"description":"ribosomal protein L28 [Source:HGNC Symbol;Acc:HGNC:10330]"}, {"versioned_ensembl_gene_id":"ENSG00000254869.1","gene_symbol":"AC068389.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60652502,"end":60653561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102890.14","gene_symbol":"ELMO3","gene_name":"engulfment and cell motility 3 [Source:HGNC Symbol;Acc:HGNC:17289]","synonyms":"FLJ13824,ELMO-3,CED12,CED-12","biotype":"protein_coding","ncbi_id":"79767","summary":"The protein encoded by this gene is similar to a C. elegans protein that functions in phagocytosis of apoptotic cells and in cell migration. Other members of this small family of engulfment and cell motility (ELMO) proteins have been shown to interact with the dedicator of cyto-kinesis 1 protein to promote phagocytosis and effect cell shape changes. [provided by RefSeq, Jul 2008]","start":67199111,"end":67204029,"strand":1,"description":"engulfment and cell motility 3 [Source:HGNC Symbol;Acc:HGNC:17289]"}, {"versioned_ensembl_gene_id":"ENSG00000251011.5","gene_symbol":"TMEM108-AS1","gene_name":"TMEM108 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50307]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927455","summary":null,"start":133246106,"end":133257188,"strand":-1,"description":"TMEM108 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50307]"}, {"versioned_ensembl_gene_id":"ENSG00000267590.1","gene_symbol":"NDUFA3P1","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131388","summary":null,"start":44297104,"end":44297355,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45043]"}, {"versioned_ensembl_gene_id":"ENSG00000258572.1","gene_symbol":"AL133467.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95516136,"end":95517911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134986.13","gene_symbol":"NREP","gene_name":"neuronal regeneration related protein [Source:HGNC Symbol;Acc:HGNC:16834]","synonyms":"PRO1873,P311,D4S114,C5orf13,PTZ17,SEZ17","biotype":"protein_coding","ncbi_id":"9315","summary":null,"start":111662621,"end":111997464,"strand":-1,"description":"neuronal regeneration related protein [Source:HGNC Symbol;Acc:HGNC:16834]"}, {"versioned_ensembl_gene_id":"ENSG00000277340.1","gene_symbol":"AL591926.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41573156,"end":41573453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236765.6","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31951992,"end":31954474,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000133665.12","gene_symbol":"DYDC2","gene_name":"DPY30 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23468]","synonyms":"MGC16186,bA36D19.6","biotype":"protein_coding","ncbi_id":"84332","summary":"This gene encodes a member of a family of proteins that contains a DPY30 domain. This gene locus overlaps with a closely related gene on the opposite strand. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":80344745,"end":80368073,"strand":1,"description":"DPY30 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23468]"}, {"versioned_ensembl_gene_id":"ENSG00000232565.1","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478955","summary":null,"start":31982173,"end":31985702,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000268833.1","gene_symbol":"AC243967.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41757898,"end":41786893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149115.13","gene_symbol":"TNKS1BP1","gene_name":"tankyrase 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19081]","synonyms":"TAB182,KIAA1741,FLJ45975","biotype":"protein_coding","ncbi_id":"85456","summary":null,"start":57299638,"end":57324952,"strand":-1,"description":"tankyrase 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19081]"}, {"versioned_ensembl_gene_id":"ENSG00000214376.5","gene_symbol":"VSTM5","gene_name":"V-set and transmembrane domain containing 5 [Source:HGNC Symbol;Acc:HGNC:34443]","synonyms":"LOC387804,C11orf90","biotype":"protein_coding","ncbi_id":"387804","summary":null,"start":93818232,"end":93850531,"strand":-1,"description":"V-set and transmembrane domain containing 5 [Source:HGNC Symbol;Acc:HGNC:34443]"}, {"versioned_ensembl_gene_id":"ENSG00000213655.4","gene_symbol":"AC010493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123236079,"end":123236370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225155.4","gene_symbol":"TOMM22P5","gene_name":"TOMM22 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38741]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390007","summary":null,"start":118643760,"end":118644198,"strand":1,"description":"TOMM22 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38741]"}, {"versioned_ensembl_gene_id":"ENSG00000112530.11","gene_symbol":"PACRG","gene_name":"parkin coregulated [Source:HGNC Symbol;Acc:HGNC:19152]","synonyms":"PARK2CRG,HAK005771,Glup,FLJ32724","biotype":"protein_coding","ncbi_id":"135138","summary":"This gene encodes a protein that is conserved across metazoans. In vertebrates, this gene is linked in a head-to-head arrangement with the adjacent parkin gene, which is associated with autosomal recessive juvenile Parkinson's disease. These genes are co-regulated in various tissues and they share a bi-directional promoter. Both genes are associated with susceptibility to leprosy. The parkin co-regulated gene protein forms a large molecular complex with chaperones, including heat shock proteins 70 and 90, and chaperonin components. This protein is also a component of Lewy bodies in Parkinson's disease patients, and it suppresses unfolded Pael receptor-induced neuronal cell death. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":162727132,"end":163315492,"strand":1,"description":"parkin coregulated [Source:HGNC Symbol;Acc:HGNC:19152]"}, {"versioned_ensembl_gene_id":"ENSG00000167645.16","gene_symbol":"YIF1B","gene_name":"Yip1 interacting factor homolog B, membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:30511]","synonyms":"FinGER8","biotype":"protein_coding","ncbi_id":"90522","summary":null,"start":38305104,"end":38317273,"strand":-1,"description":"Yip1 interacting factor homolog B, membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:30511]"}, {"versioned_ensembl_gene_id":"ENSG00000253759.1","gene_symbol":"IGHV3-57","gene_name":"immunoglobulin heavy variable 3-57 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5612]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28418","summary":null,"start":106618894,"end":106619173,"strand":-1,"description":"immunoglobulin heavy variable 3-57 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5612]"}, {"versioned_ensembl_gene_id":"ENSG00000253131.1","gene_symbol":"IGHV7-56","gene_name":"immunoglobulin heavy variable 7-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5667]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28380","summary":null,"start":106609762,"end":106610196,"strand":-1,"description":"immunoglobulin heavy variable 7-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5667]"}, {"versioned_ensembl_gene_id":"ENSG00000254395.1","gene_symbol":"IGHV4-55","gene_name":"immunoglobulin heavy variable 4-55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5653]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28393","summary":null,"start":106606101,"end":106606551,"strand":-1,"description":"immunoglobulin heavy variable 4-55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5653]"}, {"versioned_ensembl_gene_id":"ENSG00000160471.12","gene_symbol":"COX6B2","gene_name":"cytochrome c oxidase subunit 6B2 [Source:HGNC Symbol;Acc:HGNC:24380]","synonyms":"FLJ32865,CT59,COXVIB2","biotype":"protein_coding","ncbi_id":"125965","summary":null,"start":55349306,"end":55354814,"strand":-1,"description":"cytochrome c oxidase subunit 6B2 [Source:HGNC Symbol;Acc:HGNC:24380]"}, {"versioned_ensembl_gene_id":"ENSG00000253386.1","gene_symbol":"IGHVII-49-1","gene_name":"immunoglobulin heavy variable (II)-49-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5683]","synonyms":"IGHV(II)-49-1","biotype":"IG_V_pseudogene","ncbi_id":"28364","summary":null,"start":106564375,"end":106564598,"strand":-1,"description":"immunoglobulin heavy variable (II)-49-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5683]"}, {"versioned_ensembl_gene_id":"ENSG00000278647.1","gene_symbol":"CDK2AP2P1","gene_name":"cyclin dependent kinase 2 associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38492]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100289027","summary":null,"start":41280460,"end":41280787,"strand":1,"description":"cyclin dependent kinase 2 associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38492]"}, {"versioned_ensembl_gene_id":"ENSG00000204446.4","gene_symbol":"C9orf170","gene_name":"chromosome 9 open reading frame 170 [Source:HGNC Symbol;Acc:HGNC:33817]","synonyms":"FLJ45537","biotype":"lincRNA","ncbi_id":"401535","summary":null,"start":87148644,"end":87159556,"strand":1,"description":"chromosome 9 open reading frame 170 [Source:HGNC Symbol;Acc:HGNC:33817]"}, {"versioned_ensembl_gene_id":"ENSG00000259290.1","gene_symbol":"AP001007.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":125188115,"end":125191404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096171.14","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31759699,"end":31778134,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000182687.3","gene_symbol":"GALR2","gene_name":"galanin receptor 2 [Source:HGNC Symbol;Acc:HGNC:4133]","synonyms":"GALNR2","biotype":"protein_coding","ncbi_id":"8811","summary":"Galanin is an important neuromodulator present in the brain, gastrointestinal system, and hypothalamopituitary axis. It is a 30-amino acid non-C-terminally amidated peptide that potently stimulates growth hormone secretion, inhibits cardiac vagal slowing of heart rate, abolishes sinus arrhythmia, and inhibits postprandial gastrointestinal motility. The actions of galanin are mediated through interaction with specific membrane receptors that are members of the 7-transmembrane family of G protein-coupled receptors. GALR2 interacts with the N-terminal residues of the galanin peptide. The primary signaling mechanism for GALR2 is through the phospholipase C/protein kinase C pathway (via Gq), in contrast to GALR1, which communicates its intracellular signal by inhibition of adenylyl cyclase through Gi. However, it has been demonstrated that GALR2 couples efficiently to both the Gq and Gi proteins to simultaneously activate 2 independent signal transduction pathways. [provided by RefSeq, Jul 2008]","start":76074794,"end":76077541,"strand":1,"description":"galanin receptor 2 [Source:HGNC Symbol;Acc:HGNC:4133]"}, {"versioned_ensembl_gene_id":"ENSG00000283952.1","gene_symbol":"AC092017.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":211082872,"end":211188533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234233.1","gene_symbol":"KCNH1-IT1","gene_name":"KCNH1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41351]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874296","summary":null,"start":211132588,"end":211133374,"strand":-1,"description":"KCNH1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41351]"}, {"versioned_ensembl_gene_id":"ENSG00000284299.1","gene_symbol":"AL590132.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":210858125,"end":211134146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276471.1","gene_symbol":"AC105265.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72080564,"end":72084641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250061.5","gene_symbol":"AC091976.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":163012265,"end":163437326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254173.1","gene_symbol":"AC091996.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162424378,"end":162427345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273775.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816442,"end":54830745,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000230734.1","gene_symbol":"RPL10P3","gene_name":"ribosomal protein L10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23300]","synonyms":"bA567J2.2","biotype":"processed_pseudogene","ncbi_id":"619445","summary":null,"start":117180628,"end":117181095,"strand":-1,"description":"ribosomal protein L10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23300]"}, {"versioned_ensembl_gene_id":"ENSG00000229105.1","gene_symbol":"ASTN2-AS1","gene_name":"ASTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51175]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128505","summary":null,"start":116504283,"end":116562293,"strand":1,"description":"ASTN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51175]"}, {"versioned_ensembl_gene_id":"ENSG00000278051.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786397,"end":54790252,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000283156.1","gene_symbol":"AC068620.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56410516,"end":56431548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270883.1","gene_symbol":"AC080078.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152317902,"end":152318364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253491.2","gene_symbol":"IGHVII-30-1","gene_name":"immunoglobulin heavy variable (II)-30-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5676]","synonyms":"IGHV(II)-30-1","biotype":"IG_V_pseudogene","ncbi_id":"28371","summary":null,"start":106342680,"end":106342980,"strand":-1,"description":"immunoglobulin heavy variable (II)-30-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5676]"}, {"versioned_ensembl_gene_id":"ENSG00000224085.3","gene_symbol":"RPL23AP41","gene_name":"ribosomal protein L23a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35634]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646685","summary":null,"start":140902194,"end":140902651,"strand":1,"description":"ribosomal protein L23a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35634]"}, {"versioned_ensembl_gene_id":"ENSG00000229272.1","gene_symbol":"AL157788.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119003536,"end":119003884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160703.15","gene_symbol":"NLRX1","gene_name":"NLR family member X1 [Source:HGNC Symbol;Acc:HGNC:29890]","synonyms":"NOD9,CLR11.3","biotype":"protein_coding","ncbi_id":"79671","summary":"The protein encoded by this gene is a member of the NLR family and localizes to the outer mitochondrial membrane. The encoded protein is a regulator of mitochondrial antivirus responses. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2013]","start":119166568,"end":119184016,"strand":1,"description":"NLR family member X1 [Source:HGNC Symbol;Acc:HGNC:29890]"}, {"versioned_ensembl_gene_id":"ENSG00000236058.3","gene_symbol":"RPL17P36","gene_name":"ribosomal protein L17 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729340","summary":null,"start":118872054,"end":118872602,"strand":-1,"description":"ribosomal protein L17 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36051]"}, {"versioned_ensembl_gene_id":"ENSG00000263280.1","gene_symbol":"AC003965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2866348,"end":2867618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100823.11","gene_symbol":"APEX1","gene_name":"apurinic/apyrimidinic endodeoxyribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:587]","synonyms":"REF1,REF-1,HAP1,APX,APEX,APEN,APE-1,APE","biotype":"protein_coding","ncbi_id":"328","summary":"The APEX gene encodes the major AP endonuclease in human cells. It encodes the APEX endonuclease, a DNA repair enzyme with apurinic/apyrimidinic (AP) activity. Such AP activity sites occur frequently in DNA molecules by spontaneous hydrolysis, by DNA damaging agents or by DNA glycosylases that remove specific abnormal bases. The AP sites are the most frequent pre-mutagenic lesions that can prevent normal DNA replication. Splice variants have been found for this gene; all encode the same protein. Disruptions in the biological functions related to APEX are associated with many various malignancies and neurodegenerative diseases.[provided by RefSeq, Dec 2019]","start":20455191,"end":20457772,"strand":1,"description":"apurinic/apyrimidinic endodeoxyribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:587]"}, {"versioned_ensembl_gene_id":"ENSG00000249655.1","gene_symbol":"AC008434.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80630313,"end":80631590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228716.6","gene_symbol":"DHFR","gene_name":"dihydrofolate reductase [Source:HGNC Symbol;Acc:HGNC:2861]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1719","summary":"Dihydrofolate reductase converts dihydrofolate into tetrahydrofolate, a methyl group shuttle required for the de novo synthesis of purines, thymidylic acid, and certain amino acids. While the functional dihydrofolate reductase gene has been mapped to chromosome 5, multiple intronless processed pseudogenes or dihydrofolate reductase-like genes have been identified on separate chromosomes. Dihydrofolate reductase deficiency has been linked to megaloblastic anemia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]","start":80626228,"end":80654983,"strand":-1,"description":"dihydrofolate reductase [Source:HGNC Symbol;Acc:HGNC:2861]"}, {"versioned_ensembl_gene_id":"ENSG00000130529.15","gene_symbol":"TRPM4","gene_name":"transient receptor potential cation channel subfamily M member 4 [Source:HGNC Symbol;Acc:HGNC:17993]","synonyms":"FLJ20041","biotype":"protein_coding","ncbi_id":"54795","summary":"The protein encoded by this gene is a calcium-activated nonselective ion channel that mediates transport of monovalent cations across membranes, thereby depolarizing the membrane. The activity of the encoded protein increases with increasing intracellular calcium concentration, but this channel does not transport calcium. [provided by RefSeq, Mar 2016]","start":49157741,"end":49211836,"strand":1,"description":"transient receptor potential cation channel subfamily M member 4 [Source:HGNC Symbol;Acc:HGNC:17993]"}, {"versioned_ensembl_gene_id":"ENSG00000284643.1","gene_symbol":"AC064853.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227598893,"end":227599255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284622.1","gene_symbol":"AC064853.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227608784,"end":227608927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256508.2","gene_symbol":"MRGPRF-AS1","gene_name":"MRGPRF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51140]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928200","summary":null,"start":69012283,"end":69018447,"strand":1,"description":"MRGPRF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51140]"}, {"versioned_ensembl_gene_id":"ENSG00000233175.2","gene_symbol":"AC008105.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45238028,"end":45241734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216639.1","gene_symbol":"AL133406.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105298149,"end":105298895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244565.1","gene_symbol":"AC073901.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115503367,"end":115504081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172935.8","gene_symbol":"MRGPRF","gene_name":"MAS related GPR family member F [Source:HGNC Symbol;Acc:HGNC:24828]","synonyms":"mrgF,MGC21621,GPR168,GPR140","biotype":"protein_coding","ncbi_id":"116535","summary":null,"start":69004395,"end":69013409,"strand":-1,"description":"MAS related GPR family member F [Source:HGNC Symbol;Acc:HGNC:24828]"}, {"versioned_ensembl_gene_id":"ENSG00000275289.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,LILRA5,CD85m,ILT10,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000236383.8","gene_symbol":"LINC00854","gene_name":"long intergenic non-protein coding RNA 854 [Source:HGNC Symbol;Acc:HGNC:43658]","synonyms":"TMEM106A-AS1","biotype":"protein_coding","ncbi_id":"100874261","summary":null,"start":43216941,"end":43305397,"strand":-1,"description":"long intergenic non-protein coding RNA 854 [Source:HGNC Symbol;Acc:HGNC:43658]"}, {"versioned_ensembl_gene_id":"ENSG00000141569.10","gene_symbol":"TRIM65","gene_name":"tripartite motif containing 65 [Source:HGNC Symbol;Acc:HGNC:27316]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201292","summary":null,"start":75880335,"end":75897003,"strand":-1,"description":"tripartite motif containing 65 [Source:HGNC Symbol;Acc:HGNC:27316]"}, {"versioned_ensembl_gene_id":"ENSG00000196123.12","gene_symbol":"KIAA0895L","gene_name":"KIAA0895 like [Source:HGNC Symbol;Acc:HGNC:34408]","synonyms":"LOC653319","biotype":"protein_coding","ncbi_id":"653319","summary":null,"start":67175602,"end":67184040,"strand":-1,"description":"KIAA0895 like [Source:HGNC Symbol;Acc:HGNC:34408]"}, {"versioned_ensembl_gene_id":"ENSG00000011485.14","gene_symbol":"PPP5C","gene_name":"protein phosphatase 5 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9322]","synonyms":"PP5,PPP5","biotype":"protein_coding","ncbi_id":"5536","summary":"This gene encodes a serine/threonine phosphatase which is a member of the protein phosphatase catalytic subunit family. Proteins in this family participate in pathways regulated by reversible phosphorylation at serine and threonine residues; many of these pathways are involved in the regulation of cell growth and differentiation. The product of this gene has been shown to participate in signaling pathways in response to hormones or cellular stress, and elevated levels of this protein may be associated with breast cancer development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2011]","start":46346994,"end":46392981,"strand":1,"description":"protein phosphatase 5 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9322]"}, {"versioned_ensembl_gene_id":"ENSG00000269151.1","gene_symbol":"AC007193.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46390515,"end":46390852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231092.1","gene_symbol":"AC012513.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216259595,"end":216266130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095981.10","gene_symbol":"KCNK16","gene_name":"potassium two pore domain channel subfamily K member 16 [Source:HGNC Symbol;Acc:HGNC:14464]","synonyms":"TALK1,TALK-1,K2p16.1","biotype":"protein_coding","ncbi_id":"83795","summary":"The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is expressed predominantly in the pancreas and is activated at alkaline pH. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008]","start":39314698,"end":39322968,"strand":-1,"description":"potassium two pore domain channel subfamily K member 16 [Source:HGNC Symbol;Acc:HGNC:14464]"}, {"versioned_ensembl_gene_id":"ENSG00000255093.2","gene_symbol":"AP002008.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":111448450,"end":111475397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249042.5","gene_symbol":"AC008771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80482293,"end":80488063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229439.3","gene_symbol":"BX000531.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489145,"end":29489550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211943.2","gene_symbol":"IGHV3-15","gene_name":"immunoglobulin heavy variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5582]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28448","summary":null,"start":106153624,"end":106154163,"strand":-1,"description":"immunoglobulin heavy variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5582]"}, {"versioned_ensembl_gene_id":"ENSG00000257893.2","gene_symbol":"LINC02404","gene_name":"long intergenic non-protein coding RNA 2404 [Source:HGNC Symbol;Acc:HGNC:53331]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369900","summary":null,"start":91877391,"end":91880655,"strand":1,"description":"long intergenic non-protein coding RNA 2404 [Source:HGNC Symbol;Acc:HGNC:53331]"}, {"versioned_ensembl_gene_id":"ENSG00000229782.1","gene_symbol":"AC118754.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4497394,"end":4499674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261528.2","gene_symbol":"AC002400.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23500905,"end":23501630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254053.1","gene_symbol":"IGHVIII-5-2","gene_name":"immunoglobulin heavy variable (III)-5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5703]","synonyms":"IGHV(III)-5-2","biotype":"IG_V_pseudogene","ncbi_id":"28353","summary":null,"start":106045600,"end":106045860,"strand":-1,"description":"immunoglobulin heavy variable (III)-5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5703]"}, {"versioned_ensembl_gene_id":"ENSG00000282122.1","gene_symbol":"AC244226.1","gene_name":"Immunoglobulin heavy variable 7-4-1 [Source:UniProtKB/Swiss-Prot;Acc:A0A0J9YVY3]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106025145,"end":106025630,"strand":-1,"description":"Immunoglobulin heavy variable 7-4-1 [Source:UniProtKB/Swiss-Prot;Acc:A0A0J9YVY3]"}, {"versioned_ensembl_gene_id":"ENSG00000271350.1","gene_symbol":"AC103792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47041027,"end":47041945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165724.5","gene_symbol":"ZMYND19","gene_name":"zinc finger MYND-type containing 19 [Source:HGNC Symbol;Acc:HGNC:21146]","synonyms":"MIZIP","biotype":"protein_coding","ncbi_id":"116225","summary":"ZMYND19 is a MYND zinc finger domain-containing protein that binds to the C terminus of melanin-concentrating hormone receptor-1 (MCHR1; MIM 601751) (Bachner et al., 2002 [PubMed 12208518]), and to the N termini of alpha-tubulin (TUBA1; MIM 191110), and beta-tubulin (TUBB; MIM 191130) (Francke et al., 2005 [PubMed 16039987]).[supplied by OMIM, Mar 2008]","start":137582079,"end":137590490,"strand":-1,"description":"zinc finger MYND-type containing 19 [Source:HGNC Symbol;Acc:HGNC:21146]"}, {"versioned_ensembl_gene_id":"ENSG00000227935.1","gene_symbol":"AL390243.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57386576,"end":57387450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254726.2","gene_symbol":"MEX3A","gene_name":"mex-3 RNA binding family member A [Source:HGNC Symbol;Acc:HGNC:33482]","synonyms":"RKHD4","biotype":"protein_coding","ncbi_id":"92312","summary":null,"start":156072013,"end":156081998,"strand":-1,"description":"mex-3 RNA binding family member A [Source:HGNC Symbol;Acc:HGNC:33482]"}, {"versioned_ensembl_gene_id":"ENSG00000253870.1","gene_symbol":"IGKV1-32","gene_name":"immunoglobulin kappa variable 1-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5736]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28934","summary":null,"start":89253571,"end":89254015,"strand":-1,"description":"immunoglobulin kappa variable 1-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5736]"}, {"versioned_ensembl_gene_id":"ENSG00000232925.2","gene_symbol":"MRPS16P2","gene_name":"mitochondrial ribosomal protein S16 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16541]","synonyms":"MRPS16P,bA379F14.1","biotype":"processed_pseudogene","ncbi_id":"128609","summary":null,"start":59113224,"end":59113631,"strand":1,"description":"mitochondrial ribosomal protein S16 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16541]"}, {"versioned_ensembl_gene_id":"ENSG00000165478.6","gene_symbol":"HEPACAM","gene_name":"hepatic and glial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:26361]","synonyms":"hepaCAM,GLIALCAM,FLJ25530","biotype":"protein_coding","ncbi_id":"220296","summary":"The protein encoded by this gene is a single-pass type I membrane protein that localizes to the cytoplasmic side of the cell membrane. The encoded protein acts as a homodimer and is involved in cell motility and cell-matrix interactions. The expression of this gene is downregulated or undetectable in many cancer cell lines, so this may be a tumor suppressor gene. [provided by RefSeq, Jul 2011]","start":124919193,"end":124936412,"strand":-1,"description":"hepatic and glial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:26361]"}, {"versioned_ensembl_gene_id":"ENSG00000225750.1","gene_symbol":"AL357500.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29144494,"end":29146994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283627.1","gene_symbol":"AL137785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89013386,"end":89025807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258990.2","gene_symbol":"MPPE1P1","gene_name":"metallophosphoesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20143]","synonyms":"MPPE1P","biotype":"processed_pseudogene","ncbi_id":"390501","summary":null,"start":89110148,"end":89111223,"strand":-1,"description":"metallophosphoesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20143]"}, {"versioned_ensembl_gene_id":"ENSG00000165861.13","gene_symbol":"ZFYVE1","gene_name":"zinc finger FYVE-type containing 1 [Source:HGNC Symbol;Acc:HGNC:13180]","synonyms":"ZNFN2A1,TAFF1,PPP1R172,KIAA1589,DFCP1","biotype":"protein_coding","ncbi_id":"53349","summary":"The FYVE domain mediates the recruitment of proteins involved in membrane trafficking and cell signaling to phosphatidylinositol 3-phosphate-containing membranes. This protein contains two zinc-binding FYVE domains in tandem and is reported to localize to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":72969451,"end":73027212,"strand":-1,"description":"zinc finger FYVE-type containing 1 [Source:HGNC Symbol;Acc:HGNC:13180]"}, {"versioned_ensembl_gene_id":"ENSG00000105063.18","gene_symbol":"PPP6R1","gene_name":"protein phosphatase 6 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:29195]","synonyms":"SAPS1,SAP190,KIAA1115","biotype":"protein_coding","ncbi_id":"22870","summary":"Protein phosphatase regulatory subunits, such as SAPS1, modulate the activity of protein phosphatase catalytic subunits by restricting substrate specificity, recruiting substrates, and determining the intracellular localization of the holoenzyme. SAPS1 is a regulatory subunit for the protein phosphatase-6 catalytic subunit (PPP6C; MIM 612725) (Stefansson and Brautigan, 2006 [PubMed 16769727]).[supplied by OMIM, Nov 2010]","start":55229780,"end":55258995,"strand":-1,"description":"protein phosphatase 6 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:29195]"}, {"versioned_ensembl_gene_id":"ENSG00000261393.1","gene_symbol":"AC007493.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50368580,"end":50371480,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271564.1","gene_symbol":"LINC02333","gene_name":"long intergenic non-protein coding RNA 2333 [Source:HGNC Symbol;Acc:HGNC:53253]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103191607","summary":null,"start":52334295,"end":52341896,"strand":1,"description":"long intergenic non-protein coding RNA 2333 [Source:HGNC Symbol;Acc:HGNC:53253]"}, {"versioned_ensembl_gene_id":"ENSG00000184100.6","gene_symbol":"BRD7P2","gene_name":"bromodomain containing 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33541]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647076","summary":null,"start":160100850,"end":160102793,"strand":1,"description":"bromodomain containing 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33541]"}, {"versioned_ensembl_gene_id":"ENSG00000217227.1","gene_symbol":"AL079341.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38587323,"end":38588529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110244.6","gene_symbol":"APOA4","gene_name":"apolipoprotein A4 [Source:HGNC Symbol;Acc:HGNC:602]","synonyms":null,"biotype":"protein_coding","ncbi_id":"337","summary":"Apoliprotein (apo) A-IV gene contains 3 exons separated by two introns. A sequence polymorphism has been identified in the 3'UTR of the third exon. The primary translation product is a 396-residue preprotein which after proteolytic processing is secreted its primary site of synthesis, the intestine, in association with chylomicron particles. Although its precise function is not known, apo A-IV is a potent activator of lecithin-cholesterol acyltransferase in vitro. [provided by RefSeq, Jul 2008]","start":116820700,"end":116823306,"strand":-1,"description":"apolipoprotein A4 [Source:HGNC Symbol;Acc:HGNC:602]"}, {"versioned_ensembl_gene_id":"ENSG00000253732.1","gene_symbol":"IGKV2-19","gene_name":"immunoglobulin kappa variable 2-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5779]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28925","summary":null,"start":89134975,"end":89135257,"strand":-1,"description":"immunoglobulin kappa variable 2-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5779]"}, {"versioned_ensembl_gene_id":"ENSG00000271916.1","gene_symbol":"AC012467.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53797764,"end":53798019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119650.12","gene_symbol":"IFT43","gene_name":"intraflagellar transport 43 [Source:HGNC Symbol;Acc:HGNC:29669]","synonyms":"MGC16028,FLJ32173,C14orf179","biotype":"protein_coding","ncbi_id":"112752","summary":"This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":75902136,"end":76084585,"strand":1,"description":"intraflagellar transport 43 [Source:HGNC Symbol;Acc:HGNC:29669]"}, {"versioned_ensembl_gene_id":"ENSG00000196131.6","gene_symbol":"VN1R2","gene_name":"vomeronasal 1 receptor 2 [Source:HGNC Symbol;Acc:HGNC:19872]","synonyms":"V1RL2","biotype":"protein_coding","ncbi_id":"317701","summary":null,"start":53258292,"end":53261837,"strand":1,"description":"vomeronasal 1 receptor 2 [Source:HGNC Symbol;Acc:HGNC:19872]"}, {"versioned_ensembl_gene_id":"ENSG00000279518.1","gene_symbol":"AC083843.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134783694,"end":134785879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189056.13","gene_symbol":"RELN","gene_name":"reelin [Source:HGNC Symbol;Acc:HGNC:9957]","synonyms":"RL,PRO1598","biotype":"protein_coding","ncbi_id":"5649","summary":"This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":103471784,"end":103989516,"strand":-1,"description":"reelin [Source:HGNC Symbol;Acc:HGNC:9957]"}, {"versioned_ensembl_gene_id":"ENSG00000227313.1","gene_symbol":"AL365500.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35896874,"end":35898963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139631.18","gene_symbol":"CSAD","gene_name":"cysteine sulfinic acid decarboxylase [Source:HGNC Symbol;Acc:HGNC:18966]","synonyms":"PCAP,CSD","biotype":"protein_coding","ncbi_id":"51380","summary":"This gene encodes a member of the group 2 decarboxylase family. A similar protein in rodents plays a role in multiple biological processes as the rate-limiting enzyme in taurine biosynthesis, catalyzing the decarboxylation of cysteinesulfinate to hypotaurine. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":53157663,"end":53180909,"strand":-1,"description":"cysteine sulfinic acid decarboxylase [Source:HGNC Symbol;Acc:HGNC:18966]"}, {"versioned_ensembl_gene_id":"ENSG00000263586.1","gene_symbol":"HID1-AS1","gene_name":"HID1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51181]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723641","summary":null,"start":74970704,"end":74975728,"strand":1,"description":"HID1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51181]"}, {"versioned_ensembl_gene_id":"ENSG00000183034.12","gene_symbol":"OTOP2","gene_name":"otopetrin 2 [Source:HGNC Symbol;Acc:HGNC:19657]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92736","summary":null,"start":74924275,"end":74933912,"strand":1,"description":"otopetrin 2 [Source:HGNC Symbol;Acc:HGNC:19657]"}, {"versioned_ensembl_gene_id":"ENSG00000234028.3","gene_symbol":"AC062029.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88627539,"end":88631821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283913.1","gene_symbol":"AL512662.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":79904898,"end":79951029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273804.1","gene_symbol":"AC138932.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14953012,"end":14953120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121897.14","gene_symbol":"LIAS","gene_name":"lipoic acid synthetase [Source:HGNC Symbol;Acc:HGNC:16429]","synonyms":"LAS","biotype":"protein_coding","ncbi_id":"11019","summary":"The protein encoded by this gene belongs to the biotin and lipoic acid synthetases family. Localized in the mitochondrion, this iron-sulfur enzyme catalyzes the final step in the de novo pathway for the biosynthesis of lipoic acid, a potent antioxidant. The deficient expression of this enzyme has been linked to conditions such as diabetes, atherosclerosis and neonatal-onset epilepsy. Alternative splicing occurs at this locus, and several transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Aug 2020]","start":39458587,"end":39485109,"strand":1,"description":"lipoic acid synthetase [Source:HGNC Symbol;Acc:HGNC:16429]"}, {"versioned_ensembl_gene_id":"ENSG00000224097.5","gene_symbol":"AC021148.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":39480255,"end":39481905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229477.3","gene_symbol":"FAM90A16P","gene_name":"family with sequence similarity 90 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:32264]","synonyms":"FAM90A16","biotype":"unprocessed_pseudogene","ncbi_id":"441323","summary":null,"start":7730739,"end":7733749,"strand":1,"description":"family with sequence similarity 90 member A16, pseudogene [Source:HGNC Symbol;Acc:HGNC:32264]"}, {"versioned_ensembl_gene_id":"ENSG00000172782.11","gene_symbol":"FADS6","gene_name":"fatty acid desaturase 6 [Source:HGNC Symbol;Acc:HGNC:30459]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283985","summary":null,"start":74877299,"end":74893781,"strand":-1,"description":"fatty acid desaturase 6 [Source:HGNC Symbol;Acc:HGNC:30459]"}, {"versioned_ensembl_gene_id":"ENSG00000126775.8","gene_symbol":"ATG14","gene_name":"autophagy related 14 [Source:HGNC Symbol;Acc:HGNC:19962]","synonyms":"KIAA0831,ATG14L","biotype":"protein_coding","ncbi_id":"22863","summary":null,"start":55366392,"end":55411858,"strand":-1,"description":"autophagy related 14 [Source:HGNC Symbol;Acc:HGNC:19962]"}, {"versioned_ensembl_gene_id":"ENSG00000233250.1","gene_symbol":"AC233728.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53432722,"end":53433032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270455.1","gene_symbol":"AC134882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11335627,"end":11337693,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228570.7","gene_symbol":"NUTM2E","gene_name":"NUT family member 2E [Source:HGNC Symbol;Acc:HGNC:23448]","synonyms":"FAM22E","biotype":"protein_coding","ncbi_id":"283008","summary":null,"start":79841358,"end":79850878,"strand":1,"description":"NUT family member 2E [Source:HGNC Symbol;Acc:HGNC:23448]"}, {"versioned_ensembl_gene_id":"ENSG00000257725.1","gene_symbol":"LINC02399","gene_name":"long intergenic non-protein coding RNA 2399 [Source:HGNC Symbol;Acc:HGNC:53326]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369891","summary":null,"start":89947693,"end":89949726,"strand":1,"description":"long intergenic non-protein coding RNA 2399 [Source:HGNC Symbol;Acc:HGNC:53326]"}, {"versioned_ensembl_gene_id":"ENSG00000258050.2","gene_symbol":"AL139316.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55196727,"end":55199013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267005.1","gene_symbol":"AC002984.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36173406,"end":36173853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149243.15","gene_symbol":"KLHL35","gene_name":"kelch like family member 35 [Source:HGNC Symbol;Acc:HGNC:26597]","synonyms":"FLJ33790","biotype":"protein_coding","ncbi_id":"283212","summary":null,"start":75422394,"end":75430629,"strand":-1,"description":"kelch like family member 35 [Source:HGNC Symbol;Acc:HGNC:26597]"}, {"versioned_ensembl_gene_id":"ENSG00000160282.13","gene_symbol":"FTCD","gene_name":"formimidoyltransferase cyclodeaminase [Source:HGNC Symbol;Acc:HGNC:3974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10841","summary":"The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]","start":46136262,"end":46155567,"strand":-1,"description":"formimidoyltransferase cyclodeaminase [Source:HGNC Symbol;Acc:HGNC:3974]"}, {"versioned_ensembl_gene_id":"ENSG00000213455.3","gene_symbol":"AC093799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98454119,"end":98454617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267681.1","gene_symbol":"AC135721.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":43144956,"end":43145255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228940.1","gene_symbol":"AL391730.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40938104,"end":40939763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256774.1","gene_symbol":"AC087241.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22596228,"end":22596551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197125.3","gene_symbol":"OR8B8","gene_name":"olfactory receptor family 8 subfamily B member 8 [Source:HGNC Symbol;Acc:HGNC:8477]","synonyms":"TPCR85","biotype":"protein_coding","ncbi_id":"26493","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124437445,"end":124445696,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 8 [Source:HGNC Symbol;Acc:HGNC:8477]"}, {"versioned_ensembl_gene_id":"ENSG00000236366.2","gene_symbol":"AL359313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142526455,"end":142637889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263657.1","gene_symbol":"AC023389.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29761103,"end":29787836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274886.1","gene_symbol":"SEPT14P17","gene_name":"septin 14 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51703]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480344","summary":null,"start":227980051,"end":227980227,"strand":1,"description":"septin 14 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51703]"}, {"versioned_ensembl_gene_id":"ENSG00000227170.1","gene_symbol":"AF178030.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115509602,"end":115511325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044574.7","gene_symbol":"HSPA5","gene_name":"heat shock protein family A (Hsp70) member 5 [Source:HGNC Symbol;Acc:HGNC:5238]","synonyms":"BiP,GRP78","biotype":"protein_coding","ncbi_id":"3309","summary":"The protein encoded by this gene is a member of the heat shock protein 70 (HSP70) family. This protein localizes to the lumen of the endoplasmic reticulum (ER) where it operates as a typical HSP70 chaperone involved in the folding and assembly of proteins in the ER and is a master regulator of ER homeostasis. During cellular stress, as during viral infection or tumorogenesis, this protein interacts with the transmembrane stress sensor proteins PERK (protein kinase R-like endoplasmic reticulum kinase), IRE1 (inositol-requiring kinase 1), and ATF6 (activating transcription factor 6) where it acts as a repressor of the unfolded protein response (UPR) and also plays a role in cellular apoptosis and senescence. Elevated expression and atypical translocation of this protein to the cell surface has been reported in viral infections and some types of cancer cells. At the cell surface this protein may facilitate viral attachment and entry to host cells. This gene is a therapeutic target for the treatment of coronavirus diseases and chemoresistant cancers. [provided by RefSeq, Jul 2020]","start":125234853,"end":125241330,"strand":-1,"description":"heat shock protein family A (Hsp70) member 5 [Source:HGNC Symbol;Acc:HGNC:5238]"}, {"versioned_ensembl_gene_id":"ENSG00000196214.10","gene_symbol":"ZNF766","gene_name":"zinc finger protein 766 [Source:HGNC Symbol;Acc:HGNC:28063]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90321","summary":null,"start":52269571,"end":52296046,"strand":1,"description":"zinc finger protein 766 [Source:HGNC Symbol;Acc:HGNC:28063]"}, {"versioned_ensembl_gene_id":"ENSG00000106692.13","gene_symbol":"FKTN","gene_name":"fukutin [Source:HGNC Symbol;Acc:HGNC:3622]","synonyms":"LGMD2M,FCMD","biotype":"protein_coding","ncbi_id":"2218","summary":"The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2010]","start":105558130,"end":105641118,"strand":1,"description":"fukutin [Source:HGNC Symbol;Acc:HGNC:3622]"}, {"versioned_ensembl_gene_id":"ENSG00000253585.1","gene_symbol":"AP003351.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94097764,"end":94104322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239900.12","gene_symbol":"ADSL","gene_name":"adenylosuccinate lyase [Source:HGNC Symbol;Acc:HGNC:291]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158","summary":"The protein encoded by this gene belongs to the lyase 1 family. It is an essential enzyme involved in purine metabolism, and catalyzes two non-sequential reactions in the de novo purine biosynthetic pathway: the conversion of succinylaminoimidazole carboxamide ribotide (SAICAR) to aminoimidazole carboxamide ribotide (AICAR) and the conversion of adenylosuccinate (S-AMP) to adenosine monophosphate (AMP). Mutations in this gene are associated with adenylosuccinase deficiency (ADSLD), a disorder marked with psychomotor retardation, epilepsy or autistic features. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":40346500,"end":40390463,"strand":1,"description":"adenylosuccinate lyase [Source:HGNC Symbol;Acc:HGNC:291]"}, {"versioned_ensembl_gene_id":"ENSG00000259452.2","gene_symbol":"AC009269.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70791013,"end":70791486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136933.16","gene_symbol":"RABEPK","gene_name":"Rab9 effector protein with kelch motifs [Source:HGNC Symbol;Acc:HGNC:16896]","synonyms":"RAB9P40,bA65N13.1","biotype":"protein_coding","ncbi_id":"10244","summary":null,"start":125200542,"end":125234158,"strand":1,"description":"Rab9 effector protein with kelch motifs [Source:HGNC Symbol;Acc:HGNC:16896]"}, {"versioned_ensembl_gene_id":"ENSG00000240405.6","gene_symbol":"SAMMSON","gene_name":"survival associated mitochondrial melanoma specific oncogenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49644]","synonyms":"LINC01212","biotype":"lincRNA","ncbi_id":"101927152","summary":null,"start":69999550,"end":70518064,"strand":1,"description":"survival associated mitochondrial melanoma specific oncogenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49644]"}, {"versioned_ensembl_gene_id":"ENSG00000110723.11","gene_symbol":"EXPH5","gene_name":"exophilin 5 [Source:HGNC Symbol;Acc:HGNC:30578]","synonyms":"SLAC2-B","biotype":"protein_coding","ncbi_id":"23086","summary":"The protein encoded by this gene is a member of the synaptotagmin-like protein (Slp) family lacking a C2 domain. It contains an N-terminal synaptotagmin-like homology domain (SHD), and is a ras-related protein Rab-27B effector protein. This protein is thought to be involved in exosome secretion and intracellular vesicle trafficking. Reduced expression of this gene results in keratin filament defects. Mutations in this gene have been associated with some cases of epidermolysis bullosa, an inherited skin fragility disorder. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":108505431,"end":108593738,"strand":-1,"description":"exophilin 5 [Source:HGNC Symbol;Acc:HGNC:30578]"}, {"versioned_ensembl_gene_id":"ENSG00000170419.10","gene_symbol":"VSTM2A","gene_name":"V-set and transmembrane domain containing 2A [Source:HGNC Symbol;Acc:HGNC:28499]","synonyms":"VSTM2,MGC33530","biotype":"protein_coding","ncbi_id":"222008","summary":null,"start":54542325,"end":54571080,"strand":1,"description":"V-set and transmembrane domain containing 2A [Source:HGNC Symbol;Acc:HGNC:28499]"}, {"versioned_ensembl_gene_id":"ENSG00000170412.16","gene_symbol":"GPRC5C","gene_name":"G protein-coupled receptor class C group 5 member C [Source:HGNC Symbol;Acc:HGNC:13309]","synonyms":"RAIG-3","biotype":"protein_coding","ncbi_id":"55890","summary":"The protein encoded by this gene is a member of the type 3 G protein-coupled receptor family. Members of this superfamily are characterized by a signature 7-transmembrane domain motif. The specific function of this protein is unknown; however, this protein may mediate the cellular effects of retinoic acid on the G protein signal transduction cascade. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":74424851,"end":74451653,"strand":1,"description":"G protein-coupled receptor class C group 5 member C [Source:HGNC Symbol;Acc:HGNC:13309]"}, {"versioned_ensembl_gene_id":"ENSG00000277480.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29827404,"end":29828384,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000272763.1","gene_symbol":"AC103702.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48635923,"end":48647023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244559.1","gene_symbol":"AC091179.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48690481,"end":48690624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204300.6","gene_symbol":"TMEM225","gene_name":"transmembrane protein 225 [Source:HGNC Symbol;Acc:HGNC:32390]","synonyms":"SPATA47,PPP1R154,PMP22CD","biotype":"protein_coding","ncbi_id":"338661","summary":null,"start":123882926,"end":123885642,"strand":-1,"description":"transmembrane protein 225 [Source:HGNC Symbol;Acc:HGNC:32390]"}, {"versioned_ensembl_gene_id":"ENSG00000254613.2","gene_symbol":"OR6M2P","gene_name":"olfactory receptor family 6 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14713]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79546","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123839035,"end":123841930,"strand":-1,"description":"olfactory receptor family 6 subfamily M member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14713]"}, {"versioned_ensembl_gene_id":"ENSG00000253298.1","gene_symbol":"LINC01845","gene_name":"long intergenic non-protein coding RNA 1845 [Source:HGNC Symbol;Acc:HGNC:27747]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285627","summary":null,"start":159448556,"end":159466276,"strand":-1,"description":"long intergenic non-protein coding RNA 1845 [Source:HGNC Symbol;Acc:HGNC:27747]"}, {"versioned_ensembl_gene_id":"ENSG00000174842.16","gene_symbol":"GLMN","gene_name":"glomulin, FKBP associated protein [Source:HGNC Symbol;Acc:HGNC:14373]","synonyms":"VMGLOM,GVM,GLML,FKBPAP,FAP48","biotype":"protein_coding","ncbi_id":"11146","summary":"This gene encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Multiple splice variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":92246402,"end":92298987,"strand":-1,"description":"glomulin, FKBP associated protein [Source:HGNC Symbol;Acc:HGNC:14373]"}, {"versioned_ensembl_gene_id":"ENSG00000124357.12","gene_symbol":"NAGK","gene_name":"N-acetylglucosamine kinase [Source:HGNC Symbol;Acc:HGNC:17174]","synonyms":"GNK","biotype":"protein_coding","ncbi_id":"55577","summary":"This gene encodes a member of the N-acetylhexosamine kinase family. The encoded protein catalyzes the conversion of N-acetyl-D-glucosamine to N-acetyl-D-glucosamine 6-phosphate, and is the major mammalian enzyme which recovers amino sugars. [provided by RefSeq, Nov 2011]","start":71064344,"end":71079805,"strand":1,"description":"N-acetylglucosamine kinase [Source:HGNC Symbol;Acc:HGNC:17174]"}, {"versioned_ensembl_gene_id":"ENSG00000256120.1","gene_symbol":"SOX5-AS1","gene_name":"SOX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53311]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928471","summary":null,"start":24223271,"end":24237965,"strand":1,"description":"SOX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53311]"}, {"versioned_ensembl_gene_id":"ENSG00000223729.1","gene_symbol":"LINC02247","gene_name":"long intergenic non-protein coding RNA 2247 [Source:HGNC Symbol;Acc:HGNC:53140]","synonyms":"ENST00000417135","biotype":"lincRNA","ncbi_id":"105376310","summary":null,"start":134293931,"end":134295397,"strand":-1,"description":"long intergenic non-protein coding RNA 2247 [Source:HGNC Symbol;Acc:HGNC:53140]"}, {"versioned_ensembl_gene_id":"ENSG00000108830.9","gene_symbol":"RND2","gene_name":"Rho family GTPase 2 [Source:HGNC Symbol;Acc:HGNC:18315]","synonyms":"Rho7,ARHN,RhoN","biotype":"protein_coding","ncbi_id":"8153","summary":"This gene encodes a member of the Rho GTPase family, whose members play a key role in the regulation of actin cytoskeleton organization in response to extracellular growth factors. This particular family member has been implicated in the regulation of neuronal morphology and endosomal trafficking. The gene localizes to chromosome 17 and is the centromeric neighbor of the breast-ovarian cancer susceptibility gene BRCA1. [provided by RefSeq, Jul 2008]","start":43025241,"end":43032036,"strand":1,"description":"Rho family GTPase 2 [Source:HGNC Symbol;Acc:HGNC:18315]"}, {"versioned_ensembl_gene_id":"ENSG00000255864.5","gene_symbol":"AC069208.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24213256,"end":24562590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214182.5","gene_symbol":"PTMAP5","gene_name":"prothymosin, alpha pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:9628]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"150928","summary":null,"start":81689911,"end":81691072,"strand":1,"description":"prothymosin, alpha pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:9628]"}, {"versioned_ensembl_gene_id":"ENSG00000176925.7","gene_symbol":"OR51F2","gene_name":"olfactory receptor family 51 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:15197]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119694","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4821321,"end":4822456,"strand":1,"description":"olfactory receptor family 51 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:15197]"}, {"versioned_ensembl_gene_id":"ENSG00000141219.15","gene_symbol":"C17orf80","gene_name":"chromosome 17 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:29601]","synonyms":"SPEP1,MIG3,HLC-8,FLJ20721","biotype":"protein_coding","ncbi_id":"55028","summary":null,"start":73232233,"end":73248947,"strand":1,"description":"chromosome 17 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:29601]"}, {"versioned_ensembl_gene_id":"ENSG00000162398.11","gene_symbol":"LEXM","gene_name":"lymphocyte expansion molecule [Source:HGNC Symbol;Acc:HGNC:26854]","synonyms":"LEM,FLJ40201,C1orf177","biotype":"protein_coding","ncbi_id":"163747","summary":null,"start":54806063,"end":54842252,"strand":1,"description":"lymphocyte expansion molecule [Source:HGNC Symbol;Acc:HGNC:26854]"}, {"versioned_ensembl_gene_id":"ENSG00000271101.1","gene_symbol":"AC005181.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71011997,"end":71013587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246263.2","gene_symbol":"UBR5-AS1","gene_name":"UBR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51661]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927221","summary":null,"start":102239394,"end":102253333,"strand":1,"description":"UBR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51661]"}, {"versioned_ensembl_gene_id":"ENSG00000259590.1","gene_symbol":"AC015660.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99395179,"end":99396593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231768.1","gene_symbol":"LINC01354","gene_name":"long intergenic non-protein coding RNA 1354 [Source:HGNC Symbol;Acc:HGNC:50581]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506795","summary":null,"start":234527891,"end":234531779,"strand":-1,"description":"long intergenic non-protein coding RNA 1354 [Source:HGNC Symbol;Acc:HGNC:50581]"}, {"versioned_ensembl_gene_id":"ENSG00000159692.15","gene_symbol":"CTBP1","gene_name":"C-terminal binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2494]","synonyms":"BARS","biotype":"protein_coding","ncbi_id":"1487","summary":"This gene encodes a protein that binds to the C-terminus of adenovirus E1A proteins. This phosphoprotein is a transcriptional repressor and may play a role during cellular proliferation. This protein and the product of a second closely related gene, CTBP2, can dimerize. Both proteins can also interact with a polycomb group protein complex which participates in regulation of gene expression during development. Alternative splicing of transcripts from this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":1211448,"end":1249953,"strand":-1,"description":"C-terminal binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2494]"}, {"versioned_ensembl_gene_id":"ENSG00000267827.5","gene_symbol":"AC011468.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":52130548,"end":52171533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251135.2","gene_symbol":"AC008565.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121040090,"end":121044032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234231.3","gene_symbol":"AC093616.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87700984,"end":87738105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183876.8","gene_symbol":"ARSI","gene_name":"arylsulfatase family member I [Source:HGNC Symbol;Acc:HGNC:32521]","synonyms":"SPG66,FLJ16069","biotype":"protein_coding","ncbi_id":"340075","summary":"This gene encodes a protein that belongs to a large family of sulfatases that hydrolyze sulfate esters and sulfamates. Members of this family play a role in several cellular processes, including hormone synthesis, cell signaling in development and degradation of macromolecules. The protein encoded by this gene is thought to be secreted, and to function in extracellular space. [provided by RefSeq, Jul 2016]","start":150296343,"end":150339307,"strand":-1,"description":"arylsulfatase family member I [Source:HGNC Symbol;Acc:HGNC:32521]"}, {"versioned_ensembl_gene_id":"ENSG00000244301.6","gene_symbol":"AOX3P","gene_name":"aldehyde oxidase 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:19049]","synonyms":"AOH1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107126360","summary":null,"start":200678233,"end":200734109,"strand":1,"description":"aldehyde oxidase 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:19049]"}, {"versioned_ensembl_gene_id":"ENSG00000167601.11","gene_symbol":"AXL","gene_name":"AXL receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:905]","synonyms":"UFO,Tyro7,JTK11,ARK","biotype":"protein_coding","ncbi_id":"558","summary":"The protein encoded by this gene is a member of the Tyro3-Axl-Mer (TAM) receptor tyrosine kinase subfamily. The encoded protein possesses an extracellular domain which is composed of two immunoglobulin-like motifs at the N-terminal, followed by two fibronectin type-III motifs. It transduces signals from the extracellular matrix into the cytoplasm by binding to the vitamin K-dependent protein growth arrest-specific 6 (Gas6). This gene may be involved in several cellular functions including growth, migration, aggregation and anti-inflammation in multiple cell types. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":41219203,"end":41261766,"strand":1,"description":"AXL receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:905]"}, {"versioned_ensembl_gene_id":"ENSG00000250031.1","gene_symbol":"AC009927.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58424588,"end":58426685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226093.1","gene_symbol":"RPS28P8","gene_name":"ribosomal protein S28 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271381","summary":null,"start":42003430,"end":42003637,"strand":1,"description":"ribosomal protein S28 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36938]"}, {"versioned_ensembl_gene_id":"ENSG00000135999.11","gene_symbol":"EPC2","gene_name":"enhancer of polycomb homolog 2 [Source:HGNC Symbol;Acc:HGNC:24543]","synonyms":"DKFZP566F2124","biotype":"protein_coding","ncbi_id":"26122","summary":null,"start":148644440,"end":148787568,"strand":1,"description":"enhancer of polycomb homolog 2 [Source:HGNC Symbol;Acc:HGNC:24543]"}, {"versioned_ensembl_gene_id":"ENSG00000232059.3","gene_symbol":"AL451007.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":244694432,"end":244694720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120093.11","gene_symbol":"HOXB3","gene_name":"homeobox B3 [Source:HGNC Symbol;Acc:HGNC:5114]","synonyms":"HOX2G,HOX2","biotype":"protein_coding","ncbi_id":"3213","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML). [provided by RefSeq, Jul 2008]","start":48548870,"end":48604912,"strand":-1,"description":"homeobox B3 [Source:HGNC Symbol;Acc:HGNC:5114]"}, {"versioned_ensembl_gene_id":"ENSG00000261245.2","gene_symbol":"AC093520.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31361278,"end":31361695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230601.6","gene_symbol":"TEX48","gene_name":"testis expressed 48 [Source:HGNC Symbol;Acc:HGNC:52393]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505478","summary":null,"start":114666434,"end":114682066,"strand":-1,"description":"testis expressed 48 [Source:HGNC Symbol;Acc:HGNC:52393]"}, {"versioned_ensembl_gene_id":"ENSG00000146477.5","gene_symbol":"SLC22A3","gene_name":"solute carrier family 22 member 3 [Source:HGNC Symbol;Acc:HGNC:10967]","synonyms":"OCT3,EMT","biotype":"protein_coding","ncbi_id":"6581","summary":"Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]","start":160348268,"end":160452581,"strand":1,"description":"solute carrier family 22 member 3 [Source:HGNC Symbol;Acc:HGNC:10967]"}, {"versioned_ensembl_gene_id":"ENSG00000133216.16","gene_symbol":"EPHB2","gene_name":"EPH receptor B2 [Source:HGNC Symbol;Acc:HGNC:3393]","synonyms":"Tyro5,Hek5,ERK,EPHT3,DRT","biotype":"protein_coding","ncbi_id":"2048","summary":"This gene encodes a member of the Eph receptor family of receptor tyrosine kinase transmembrane glycoproteins. These receptors are composed of an N-terminal glycosylated ligand-binding domain, a transmembrane region and an intracellular kinase domain. They bind ligands called ephrins and are involved in diverse cellular processes including motility, division, and differentiation. A distinguishing characteristic of Eph-ephrin signaling is that both receptors and ligands are competent to transduce a signaling cascade, resulting in bidirectional signaling. This protein belongs to a subgroup of the Eph receptors called EphB. Proteins of this subgroup are distinguished from other members of the family by sequence homology and preferential binding affinity for membrane-bound ephrin-B ligands. Allelic variants are associated with prostate and brain cancer susceptibility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015]","start":22710839,"end":22921500,"strand":1,"description":"EPH receptor B2 [Source:HGNC Symbol;Acc:HGNC:3393]"}, {"versioned_ensembl_gene_id":"ENSG00000205356.9","gene_symbol":"TECPR1","gene_name":"tectonin beta-propeller repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:22214]","synonyms":"KIAA1358,FLJ90593,FLJ23419,DKFZP434B0335","biotype":"protein_coding","ncbi_id":"25851","summary":"This gene encodes a tethering factor involved in autophagy. The encoded protein is found at autolysosomes, and is involved in targeting protein aggregates, damaged mitochondria, and bacterial pathogens for autophagy [provided by RefSeq, Nov 2012]","start":98214624,"end":98252251,"strand":-1,"description":"tectonin beta-propeller repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:22214]"}, {"versioned_ensembl_gene_id":"ENSG00000234259.3","gene_symbol":"AC008550.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119680197,"end":119681080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250895.1","gene_symbol":"AC010409.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119652523,"end":119653000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279715.1","gene_symbol":"AL161912.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79913269,"end":79915736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167646.13","gene_symbol":"DNAAF3","gene_name":"dynein axonemal assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:30492]","synonyms":"PF22,PCD,FLJ40069,FLJ36139,CILD2,C19orf51","biotype":"protein_coding","ncbi_id":"352909","summary":"The protein encoded by this gene is required for the assembly of axonemal inner and outer dynein arms and plays a role in assembling dynein complexes for transport into cilia. Defects in this gene are a cause of primary ciliary dyskinesia type 2 (CILD2). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":55158661,"end":55166722,"strand":-1,"description":"dynein axonemal assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:30492]"}, {"versioned_ensembl_gene_id":"ENSG00000172382.9","gene_symbol":"PRSS27","gene_name":"protease, serine 27 [Source:HGNC Symbol;Acc:HGNC:15475]","synonyms":"MPN,CAPH2","biotype":"protein_coding","ncbi_id":"83886","summary":"This gene is located within a large protease gene cluster on chromosome 16. It belongs to the group-1 subfamily of serine proteases. The encoded protein is a secreted tryptic serine protease and is expressed mainly in the pancreas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":2712418,"end":2720551,"strand":-1,"description":"protease, serine 27 [Source:HGNC Symbol;Acc:HGNC:15475]"}, {"versioned_ensembl_gene_id":"ENSG00000124313.13","gene_symbol":"IQSEC2","gene_name":"IQ motif and Sec7 domain 2 [Source:HGNC Symbol;Acc:HGNC:29059]","synonyms":"MRX78,MRX18,MRX1,KIAA0522","biotype":"protein_coding","ncbi_id":"23096","summary":"This gene encodes a guanine nucleotide exchange factor for the ARF family of small GTP-binding proteins. The encoded protein is a component of the postsynaptic density at excitatory synapses, and may play a critical role in cytoskeletal and synaptic organization through the activation of selected ARF substrates including ARF1 and ARF6. Mutations in this gene have been implicated in nonsyndromic X-linked cognitive disability. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":53225828,"end":53321328,"strand":-1,"description":"IQ motif and Sec7 domain 2 [Source:HGNC Symbol;Acc:HGNC:29059]"}, {"versioned_ensembl_gene_id":"ENSG00000169925.16","gene_symbol":"BRD3","gene_name":"bromodomain containing 3 [Source:HGNC Symbol;Acc:HGNC:1104]","synonyms":"RING3L,ORFX,KIAA0043","biotype":"protein_coding","ncbi_id":"8019","summary":"This gene was identified based on its homology to the gene encoding the RING3 protein, a serine/threonine kinase. The gene localizes to 9q34, a region which contains several major histocompatibility complex (MHC) genes. The function of the encoded protein is not known. [provided by RefSeq, Jul 2008]","start":134030305,"end":134068535,"strand":-1,"description":"bromodomain containing 3 [Source:HGNC Symbol;Acc:HGNC:1104]"}, {"versioned_ensembl_gene_id":"ENSG00000234508.7","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"C6orf9,G18.1a,G18.2,AGS4,G18,G18.1b,NG1","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32198436,"end":32203193,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000197838.4","gene_symbol":"CYP2A13","gene_name":"cytochrome P450 family 2 subfamily A member 13 [Source:HGNC Symbol;Acc:HGNC:2608]","synonyms":"CPAD,CYP2A","biotype":"protein_coding","ncbi_id":"1553","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. Although its endogenous substrate has not been determined, it is known to metabolize 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, a major nitrosamine specific to tobacco. This gene is part of a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. [provided by RefSeq, Jul 2008]","start":41088472,"end":41096195,"strand":1,"description":"cytochrome P450 family 2 subfamily A member 13 [Source:HGNC Symbol;Acc:HGNC:2608]"}, {"versioned_ensembl_gene_id":"ENSG00000240023.1","gene_symbol":"AL133163.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35388121,"end":35389069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258860.1","gene_symbol":"AL133163.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35362232,"end":35363628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216365.2","gene_symbol":"AL133388.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70098390,"end":70098676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242807.1","gene_symbol":"AP002371.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93052395,"end":93052827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226334.1","gene_symbol":"AL359182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104927553,"end":104928892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256975.1","gene_symbol":"AC092821.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9506347,"end":9508440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204837.4","gene_symbol":"FGF7P3","gene_name":"fibroblast growth factor 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:26671]","synonyms":"KGFLP2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"654466","summary":null,"start":39816542,"end":40106661,"strand":-1,"description":"fibroblast growth factor 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:26671]"}, {"versioned_ensembl_gene_id":"ENSG00000244687.11","gene_symbol":"UBE2V1","gene_name":"ubiquitin conjugating enzyme E2 V1 [Source:HGNC Symbol;Acc:HGNC:12494]","synonyms":"UEV1A,UEV-1,UBE2V,CROC1,CROC-1","biotype":"protein_coding","ncbi_id":"7335","summary":"Ubiquitin-conjugating E2 enzyme variant proteins constitute a distinct subfamily within the E2 protein family. They have sequence similarity to other ubiquitin-conjugating enzymes but lack the conserved cysteine residue that is critical for the catalytic activity of E2s. The protein encoded by this gene is located in the nucleus and can cause transcriptional activation of the human FOS proto-oncogene. It is thought to be involved in the control of differentiation by altering cell cycle behavior. Alternatively spliced transcript variants encoding multiple isoforms have been described for this gene, and multiple pseudogenes of this gene have been identified. Co-transcription of this gene and the neighboring upstream gene generates a rare transcript (Kua-UEV), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Apr 2012]","start":50081124,"end":50115959,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 [Source:HGNC Symbol;Acc:HGNC:12494]"}, {"versioned_ensembl_gene_id":"ENSG00000234465.10","gene_symbol":"PINLYP","gene_name":"phospholipase A2 inhibitor and LY6/PLAUR domain containing [Source:HGNC Symbol;Acc:HGNC:44206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390940","summary":null,"start":43576800,"end":43583964,"strand":1,"description":"phospholipase A2 inhibitor and LY6/PLAUR domain containing [Source:HGNC Symbol;Acc:HGNC:44206]"}, {"versioned_ensembl_gene_id":"ENSG00000235760.3","gene_symbol":"HCG2040054","gene_name":"uncharacterized LOC644093 [Source:NCBI gene;Acc:644093]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644093","summary":null,"start":47527537,"end":47535199,"strand":1,"description":"uncharacterized LOC644093 [Source:NCBI gene;Acc:644093]"}, {"versioned_ensembl_gene_id":"ENSG00000160439.15","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":55039108,"end":55071291,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000271327.1","gene_symbol":"AC010201.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89367807,"end":89369301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267422.1","gene_symbol":"AC016582.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":37779686,"end":37792865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141293.15","gene_symbol":"SKAP1","gene_name":"src kinase associated phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:15605]","synonyms":"SKAP55,SCAP1","biotype":"protein_coding","ncbi_id":"8631","summary":"This gene encodes a T cell adaptor protein, a class of intracellular molecules with modular domains capable of recruiting additional proteins but that exhibit no intrinsic enzymatic activity. The encoded protein contains a unique N-terminal region followed by a PH domain and C-terminal SH3 domain. Along with the adhesion and degranulation-promoting adaptor protein, the encoded protein plays a critical role in inside-out signaling by coupling T-cell antigen receptor stimulation to the activation of integrins. [provided by RefSeq, Jul 2008]","start":48133440,"end":48430275,"strand":-1,"description":"src kinase associated phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:15605]"}, {"versioned_ensembl_gene_id":"ENSG00000236175.3","gene_symbol":"SSU72P6","gene_name":"SSU72 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643263","summary":null,"start":4278705,"end":4279192,"strand":1,"description":"SSU72 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43625]"}, {"versioned_ensembl_gene_id":"ENSG00000270855.1","gene_symbol":"AC099849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22418829,"end":22419294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166268.10","gene_symbol":"MYRFL","gene_name":"myelin regulatory factor-like [Source:HGNC Symbol;Acc:HGNC:26316]","synonyms":"FLJ25056,C12orf28,C12orf15,bcm1377","biotype":"protein_coding","ncbi_id":"196446","summary":null,"start":69825304,"end":69959097,"strand":1,"description":"myelin regulatory factor-like [Source:HGNC Symbol;Acc:HGNC:26316]"}, {"versioned_ensembl_gene_id":"ENSG00000141574.7","gene_symbol":"SECTM1","gene_name":"secreted and transmembrane 1 [Source:HGNC Symbol;Acc:HGNC:10707]","synonyms":"K12","biotype":"protein_coding","ncbi_id":"6398","summary":"This gene encodes a transmembrane and secreted protein with characteristics of a type 1a transmembrane protein. It is found in a perinuclear Golgi-like pattern and thought to be involved in hematopoietic and/or immune system processes. [provided by RefSeq, Jul 2008]","start":82321024,"end":82334074,"strand":-1,"description":"secreted and transmembrane 1 [Source:HGNC Symbol;Acc:HGNC:10707]"}, {"versioned_ensembl_gene_id":"ENSG00000156931.15","gene_symbol":"VPS8","gene_name":"VPS8, CORVET complex subunit [Source:HGNC Symbol;Acc:HGNC:29122]","synonyms":"KIAA0804,FLJ32099","biotype":"protein_coding","ncbi_id":"23355","summary":null,"start":184812143,"end":185052614,"strand":1,"description":"VPS8, CORVET complex subunit [Source:HGNC Symbol;Acc:HGNC:29122]"}, {"versioned_ensembl_gene_id":"ENSG00000231548.2","gene_symbol":"OR55B1P","gene_name":"olfactory receptor family 55 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15241]","synonyms":"OR55C1P,OR55B2P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"390030","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4146112,"end":4151104,"strand":-1,"description":"olfactory receptor family 55 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15241]"}, {"versioned_ensembl_gene_id":"ENSG00000257580.1","gene_symbol":"AC008055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98317741,"end":98318349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235106.9","gene_symbol":"LINC00094","gene_name":"long intergenic non-protein coding RNA 94 [Source:HGNC Symbol;Acc:HGNC:24742]","synonyms":"NCRNA00094,FLJ35348,bA374P20.3","biotype":"protein_coding","ncbi_id":"266655","summary":null,"start":134025439,"end":134034666,"strand":1,"description":"long intergenic non-protein coding RNA 94 [Source:HGNC Symbol;Acc:HGNC:24742]"}, {"versioned_ensembl_gene_id":"ENSG00000231744.1","gene_symbol":"AL669818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124598707,"end":124599580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205562.2","gene_symbol":"AL049775.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85524432,"end":85529988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197429.10","gene_symbol":"IPP","gene_name":"intracisternal A particle-promoted polypeptide [Source:HGNC Symbol;Acc:HGNC:6108]","synonyms":"KLHL27","biotype":"protein_coding","ncbi_id":"3652","summary":"The protein encoded by this gene is a member of the kelch family of proteins, which is characterized by a 50 amino acid repeat which interacts with actin. Transcript variants have been described but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":45694324,"end":45750650,"strand":-1,"description":"intracisternal A particle-promoted polypeptide [Source:HGNC Symbol;Acc:HGNC:6108]"}, {"versioned_ensembl_gene_id":"ENSG00000162757.4","gene_symbol":"C1orf74","gene_name":"chromosome 1 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:26319]","synonyms":"URLC4,FLJ25078","biotype":"protein_coding","ncbi_id":"148304","summary":null,"start":209779208,"end":209784559,"strand":-1,"description":"chromosome 1 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:26319]"}, {"versioned_ensembl_gene_id":"ENSG00000230204.1","gene_symbol":"FTH1P5","gene_name":"ferritin heavy chain 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3996]","synonyms":"FTHP1,FTHL5","biotype":"processed_pseudogene","ncbi_id":"2509","summary":null,"start":50912712,"end":50913256,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3996]"}, {"versioned_ensembl_gene_id":"ENSG00000104915.14","gene_symbol":"STX10","gene_name":"syntaxin 10 [Source:HGNC Symbol;Acc:HGNC:11428]","synonyms":"SYN10,hsyn10","biotype":"protein_coding","ncbi_id":"8677","summary":"This gene belongs to the syntaxin family and encodes a soluble N-ethylmaleimide sensitive factor attachment protein receptor (SNARE). The encoded protein is involved in docking and fusion events at the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":13144058,"end":13150383,"strand":-1,"description":"syntaxin 10 [Source:HGNC Symbol;Acc:HGNC:11428]"}, {"versioned_ensembl_gene_id":"ENSG00000229454.1","gene_symbol":"AL157882.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85756042,"end":85765112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159592.10","gene_symbol":"GPBP1L1","gene_name":"GC-rich promoter binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28843]","synonyms":"SP192","biotype":"protein_coding","ncbi_id":"60313","summary":null,"start":45627304,"end":45688113,"strand":-1,"description":"GC-rich promoter binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28843]"}, {"versioned_ensembl_gene_id":"ENSG00000105755.7","gene_symbol":"ETHE1","gene_name":"ETHE1, persulfide dioxygenase [Source:HGNC Symbol;Acc:HGNC:23287]","synonyms":"YF13H12,HSCO","biotype":"protein_coding","ncbi_id":"23474","summary":"This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":43506719,"end":43527244,"strand":-1,"description":"ETHE1, persulfide dioxygenase [Source:HGNC Symbol;Acc:HGNC:23287]"}, {"versioned_ensembl_gene_id":"ENSG00000103260.8","gene_symbol":"METRN","gene_name":"meteorin, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:14151]","synonyms":"MGC2601,C16orf23","biotype":"protein_coding","ncbi_id":"79006","summary":"Meteorin regulates glial cell differentiation and promotes the formation of axonal networks during neurogenesis (Nishino et al., 2004 [PubMed 15085178]).[supplied by OMIM, Mar 2008]","start":715115,"end":719655,"strand":1,"description":"meteorin, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:14151]"}, {"versioned_ensembl_gene_id":"ENSG00000259605.3","gene_symbol":"AC074212.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45764785,"end":45769806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124216.3","gene_symbol":"SNAI1","gene_name":"snail family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:11128]","synonyms":"SNAIL1,SNAIL,SNAH,SNA,SLUGH2","biotype":"protein_coding","ncbi_id":"6615","summary":"The Drosophila embryonic protein snail is a zinc finger transcriptional repressor which downregulates the expression of ectodermal genes within the mesoderm. The nuclear protein encoded by this gene is structurally similar to the Drosophila snail protein, and is also thought to be critical for mesoderm formation in the developing embryo. At least two variants of a similar processed pseudogene have been found on chromosome 2. [provided by RefSeq, Jul 2008]","start":49982999,"end":49988886,"strand":1,"description":"snail family transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:11128]"}, {"versioned_ensembl_gene_id":"ENSG00000227279.1","gene_symbol":"AC110015.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27954519,"end":27963687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170558.8","gene_symbol":"CDH2","gene_name":"cadherin 2 [Source:HGNC Symbol;Acc:HGNC:1759]","synonyms":"NCAD,CDHN,CD325","biotype":"protein_coding","ncbi_id":"1000","summary":"This gene encodes a classical cadherin and member of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein is proteolytically processed to generate a calcium-dependent cell adhesion molecule and glycoprotein. This protein plays a role in the establishment of left-right asymmetry, development of the nervous system and the formation of cartilage and bone. [provided by RefSeq, Nov 2015]","start":27950966,"end":28177446,"strand":-1,"description":"cadherin 2 [Source:HGNC Symbol;Acc:HGNC:1759]"}, {"versioned_ensembl_gene_id":"ENSG00000141448.8","gene_symbol":"GATA6","gene_name":"GATA binding protein 6 [Source:HGNC Symbol;Acc:HGNC:4174]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2627","summary":"This gene is a member of a small family of zinc finger transcription factors that play an important role in the regulation of cellular differentiation and organogenesis during vertebrate development. This gene is expressed during early embryogenesis and localizes to endo- and mesodermally derived cells during later embryogenesis and thereby plays an important role in gut, lung, and heart development. Mutations in this gene are associated with several congenital defects. [provided by RefSeq, Mar 2012]","start":22169443,"end":22202528,"strand":1,"description":"GATA binding protein 6 [Source:HGNC Symbol;Acc:HGNC:4174]"}, {"versioned_ensembl_gene_id":"ENSG00000111344.11","gene_symbol":"RASAL1","gene_name":"RAS protein activator like 1 [Source:HGNC Symbol;Acc:HGNC:9873]","synonyms":"RASAL","biotype":"protein_coding","ncbi_id":"8437","summary":"The protein encoded by this gene is member of the GAP1 family of GTPase-activating proteins. These proteins stimulate the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. This particular family member contains domains which are characteristic of the GAP1 subfamily of RasGAP proteins but, in contrast to the other GAP1 family members, this protein is strongly and selectively expressed in endocrine tissues. Alternatively spliced transcript variants that encode different isoforms have been described [provided by RefSeq, Jul 2010]","start":113098819,"end":113136239,"strand":-1,"description":"RAS protein activator like 1 [Source:HGNC Symbol;Acc:HGNC:9873]"}, {"versioned_ensembl_gene_id":"ENSG00000189253.7","gene_symbol":"TRIM64B","gene_name":"tripartite motif containing 64B [Source:HGNC Symbol;Acc:HGNC:37147]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642446","summary":null,"start":89869282,"end":89876017,"strand":-1,"description":"tripartite motif containing 64B [Source:HGNC Symbol;Acc:HGNC:37147]"}, {"versioned_ensembl_gene_id":"ENSG00000279266.1","gene_symbol":"AC068860.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20131730,"end":20135465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243050.1","gene_symbol":"RPL30P10","gene_name":"ribosomal protein L30 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36822]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270982","summary":null,"start":57392546,"end":57392882,"strand":1,"description":"ribosomal protein L30 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36822]"}, {"versioned_ensembl_gene_id":"ENSG00000139370.11","gene_symbol":"SLC15A4","gene_name":"solute carrier family 15 member 4 [Source:HGNC Symbol;Acc:HGNC:23090]","synonyms":"PTR4,PHT1","biotype":"protein_coding","ncbi_id":"121260","summary":null,"start":128793191,"end":128823983,"strand":-1,"description":"solute carrier family 15 member 4 [Source:HGNC Symbol;Acc:HGNC:23090]"}, {"versioned_ensembl_gene_id":"ENSG00000225528.3","gene_symbol":"Z82206.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":39960397,"end":39964718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162062.14","gene_symbol":"C16orf59","gene_name":"chromosome 16 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:25849]","synonyms":"FLJ13909","biotype":"protein_coding","ncbi_id":"80178","summary":null,"start":2460080,"end":2464963,"strand":1,"description":"chromosome 16 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:25849]"}, {"versioned_ensembl_gene_id":"ENSG00000229773.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28860338,"end":28864060,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000263611.1","gene_symbol":"AC068408.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27397952,"end":27401904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278816.1","gene_symbol":"AL121890.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5061037,"end":5061340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212807.2","gene_symbol":"OR2A42","gene_name":"olfactory receptor family 2 subfamily A member 42 [Source:HGNC Symbol;Acc:HGNC:31230]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402317","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144228244,"end":144239605,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 42 [Source:HGNC Symbol;Acc:HGNC:31230]"}, {"versioned_ensembl_gene_id":"ENSG00000163581.13","gene_symbol":"SLC2A2","gene_name":"solute carrier family 2 member 2 [Source:HGNC Symbol;Acc:HGNC:11006]","synonyms":"GLUT2","biotype":"protein_coding","ncbi_id":"6514","summary":"This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":170996348,"end":171026750,"strand":-1,"description":"solute carrier family 2 member 2 [Source:HGNC Symbol;Acc:HGNC:11006]"}, {"versioned_ensembl_gene_id":"ENSG00000221933.3","gene_symbol":"OR2A25","gene_name":"olfactory receptor family 2 subfamily A member 25 [Source:HGNC Symbol;Acc:HGNC:19562]","synonyms":"OR2A27,OR2A25P","biotype":"protein_coding","ncbi_id":"392138","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144069811,"end":144075870,"strand":1,"description":"olfactory receptor family 2 subfamily A member 25 [Source:HGNC Symbol;Acc:HGNC:19562]"}, {"versioned_ensembl_gene_id":"ENSG00000204246.3","gene_symbol":"OR13C3","gene_name":"olfactory receptor family 13 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:14704]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138803","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104535749,"end":104536856,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:14704]"}, {"versioned_ensembl_gene_id":"ENSG00000226031.5","gene_symbol":"FGF13-AS1","gene_name":"FGF13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44264]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129662","summary":null,"start":138711452,"end":138716617,"strand":1,"description":"FGF13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44264]"}, {"versioned_ensembl_gene_id":"ENSG00000240305.1","gene_symbol":"AC091152.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44719760,"end":44720597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234096.9","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTNL11,BTN6","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29657097,"end":29672487,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000236277.1","gene_symbol":"NIPA2P5","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42045]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874488","summary":null,"start":79090783,"end":79094119,"strand":1,"description":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42045]"}, {"versioned_ensembl_gene_id":"ENSG00000122687.17","gene_symbol":"MRM2","gene_name":"mitochondrial rRNA methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16352]","synonyms":"RRMJ2,FTSJ2,FJH1","biotype":"protein_coding","ncbi_id":"29960","summary":"The protein encoded by this gene is a member of the S-adenosylmethionine-binding protein family. It is a nucleolar protein and it may be involved in the processing and modification of rRNA. This gene has been suggested to be involved in cell cycle control and DNA repair. [provided by RefSeq, Jul 2008]","start":2234231,"end":2242198,"strand":-1,"description":"mitochondrial rRNA methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16352]"}, {"versioned_ensembl_gene_id":"ENSG00000228683.1","gene_symbol":"AC016820.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78696062,"end":78697022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057294.14","gene_symbol":"PKP2","gene_name":"plakophilin 2 [Source:HGNC Symbol;Acc:HGNC:9024]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5318","summary":"This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This gene product may regulate the signaling activity of beta-catenin. Two alternately spliced transcripts encoding two protein isoforms have been identified. A processed pseudogene with high similarity to this locus has been mapped to chromosome 12p13. [provided by RefSeq, Jul 2008]","start":32790745,"end":32896840,"strand":-1,"description":"plakophilin 2 [Source:HGNC Symbol;Acc:HGNC:9024]"}, {"versioned_ensembl_gene_id":"ENSG00000259054.1","gene_symbol":"LINC02332","gene_name":"long intergenic non-protein coding RNA 2332 [Source:HGNC Symbol;Acc:HGNC:53252]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370400","summary":null,"start":22556311,"end":22557062,"strand":-1,"description":"long intergenic non-protein coding RNA 2332 [Source:HGNC Symbol;Acc:HGNC:53252]"}, {"versioned_ensembl_gene_id":"ENSG00000071991.8","gene_symbol":"CDH19","gene_name":"cadherin 19 [Source:HGNC Symbol;Acc:HGNC:1758]","synonyms":"CDH7","biotype":"protein_coding","ncbi_id":"28513","summary":"This gene is one of three related type II cadherin genes situated in a cluster on chromosome 18. The encoded protein is a calcium dependent cell-cell adhesion glycoprotein containing five extracellular cadherin repeats. Loss of cadherins may be associated with cancer formation. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Aug 2012]","start":66501083,"end":66604138,"strand":-1,"description":"cadherin 19 [Source:HGNC Symbol;Acc:HGNC:1758]"}, {"versioned_ensembl_gene_id":"ENSG00000256452.1","gene_symbol":"AP003170.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113818077,"end":113822458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120709.10","gene_symbol":"FAM53C","gene_name":"family with sequence similarity 53 member C [Source:HGNC Symbol;Acc:HGNC:1336]","synonyms":"C5orf6","biotype":"protein_coding","ncbi_id":"51307","summary":"The protein encoded by this gene belongs to the FAM53 protein family. FAM53 protein family members bind to a transcriptional regulator that modulates cell proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":138331935,"end":138349729,"strand":1,"description":"family with sequence similarity 53 member C [Source:HGNC Symbol;Acc:HGNC:1336]"}, {"versioned_ensembl_gene_id":"ENSG00000270690.1","gene_symbol":"AC105129.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65458574,"end":65459534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230848.1","gene_symbol":"AL360268.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128039135,"end":128057362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042317.16","gene_symbol":"SPATA7","gene_name":"spermatogenesis associated 7 [Source:HGNC Symbol;Acc:HGNC:20423]","synonyms":"LCA3,HSD3","biotype":"protein_coding","ncbi_id":"55812","summary":"This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":88384924,"end":88470350,"strand":1,"description":"spermatogenesis associated 7 [Source:HGNC Symbol;Acc:HGNC:20423]"}, {"versioned_ensembl_gene_id":"ENSG00000283096.1","gene_symbol":"AL731555.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78176928,"end":78178186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234522.1","gene_symbol":"AC073587.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":120434983,"end":120440376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223455.1","gene_symbol":"AL355298.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120069980,"end":120070159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240440.1","gene_symbol":"AC007879.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207235299,"end":207237875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112584.13","gene_symbol":"FAM120B","gene_name":"family with sequence similarity 120B [Source:HGNC Symbol;Acc:HGNC:21109]","synonyms":"CCPG,PGCC1,KIAA1838","biotype":"protein_coding","ncbi_id":"84498","summary":null,"start":170290703,"end":170407065,"strand":1,"description":"family with sequence similarity 120B [Source:HGNC Symbol;Acc:HGNC:21109]"}, {"versioned_ensembl_gene_id":"ENSG00000255757.1","gene_symbol":"AC087894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127876999,"end":127877516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262655.3","gene_symbol":"SPON1","gene_name":"spondin 1 [Source:HGNC Symbol;Acc:HGNC:11252]","synonyms":"KIAA0762,f-spondin","biotype":"protein_coding","ncbi_id":"10418","summary":null,"start":13962689,"end":14267884,"strand":1,"description":"spondin 1 [Source:HGNC Symbol;Acc:HGNC:11252]"}, {"versioned_ensembl_gene_id":"ENSG00000235423.8","gene_symbol":"AC068768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123252030,"end":123261483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213994.3","gene_symbol":"AL157395.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6197612,"end":6202693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276537.4","gene_symbol":"TTYH1","gene_name":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57348","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-independent, volume-sensitive large conductance chloride(-) channel. Three transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jan 2011]","start":54347370,"end":54369057,"strand":1,"description":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]"}, {"versioned_ensembl_gene_id":"ENSG00000108854.15","gene_symbol":"SMURF2","gene_name":"SMAD specific E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16809]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64750","summary":null,"start":64542295,"end":64662068,"strand":-1,"description":"SMAD specific E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16809]"}, {"versioned_ensembl_gene_id":"ENSG00000230650.1","gene_symbol":"AC140479.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110360608,"end":110363737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175018.12","gene_symbol":"TEX36","gene_name":"testis expressed 36 [Source:HGNC Symbol;Acc:HGNC:31653]","synonyms":"C10orf122,bA383C5.1","biotype":"protein_coding","ncbi_id":"387718","summary":null,"start":125576522,"end":125683144,"strand":-1,"description":"testis expressed 36 [Source:HGNC Symbol;Acc:HGNC:31653]"}, {"versioned_ensembl_gene_id":"ENSG00000116882.14","gene_symbol":"HAO2","gene_name":"hydroxyacid oxidase 2 [Source:HGNC Symbol;Acc:HGNC:4810]","synonyms":"HAOX2,GIG16","biotype":"protein_coding","ncbi_id":"51179","summary":"This gene is one of three related genes that have 2-hydroxyacid oxidase activity. The encoded protein localizes to the peroxisome has the highest activity toward the substrate 2-hydroxypalmitate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":119368779,"end":119394130,"strand":1,"description":"hydroxyacid oxidase 2 [Source:HGNC Symbol;Acc:HGNC:4810]"}, {"versioned_ensembl_gene_id":"ENSG00000283167.1","gene_symbol":"AC140479.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110335525,"end":110348944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236971.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SUMO2P,SMT3Bp,dJ271M21,SMT3H2P","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29636180,"end":29636463,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000088002.11","gene_symbol":"SULT2B1","gene_name":"sulfotransferase family 2B member 1 [Source:HGNC Symbol;Acc:HGNC:11459]","synonyms":"HSST2","biotype":"protein_coding","ncbi_id":"6820","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene sulfates dehydroepiandrosterone but not 4-nitrophenol, a typical substrate for the phenol and estrogen sulfotransferase subfamilies. Two alternatively spliced variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]","start":48552075,"end":48599425,"strand":1,"description":"sulfotransferase family 2B member 1 [Source:HGNC Symbol;Acc:HGNC:11459]"}, {"versioned_ensembl_gene_id":"ENSG00000036257.12","gene_symbol":"CUL3","gene_name":"cullin 3 [Source:HGNC Symbol;Acc:HGNC:2553]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8452","summary":"This gene encodes a member of the cullin protein family. The encoded protein plays a critical role in the polyubiquitination and subsequent degradation of specific protein substrates as the core component and scaffold protein of an E3 ubiquitin ligase complex. Complexes including the encoded protein may also play a role in late endosome maturation. Mutations in this gene are a cause of type 2E pseudohypoaldosteronism. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":224470150,"end":224585397,"strand":-1,"description":"cullin 3 [Source:HGNC Symbol;Acc:HGNC:2553]"}, {"versioned_ensembl_gene_id":"ENSG00000215120.2","gene_symbol":"AL590763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71527814,"end":71530225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250341.1","gene_symbol":"LINC02510","gene_name":"long intergenic non-protein coding RNA 2510 [Source:HGNC Symbol;Acc:HGNC:53499]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729307","summary":null,"start":137193756,"end":137198367,"strand":1,"description":"long intergenic non-protein coding RNA 2510 [Source:HGNC Symbol;Acc:HGNC:53499]"}, {"versioned_ensembl_gene_id":"ENSG00000258733.5","gene_symbol":"LINC02328","gene_name":"long intergenic non-protein coding RNA 2328 [Source:HGNC Symbol;Acc:HGNC:53248]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928767","summary":null,"start":85934710,"end":86129778,"strand":1,"description":"long intergenic non-protein coding RNA 2328 [Source:HGNC Symbol;Acc:HGNC:53248]"}, {"versioned_ensembl_gene_id":"ENSG00000258912.1","gene_symbol":"LINC02316","gene_name":"long intergenic non-protein coding RNA 2316 [Source:HGNC Symbol;Acc:HGNC:53235]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724380","summary":null,"start":86014686,"end":86062960,"strand":-1,"description":"long intergenic non-protein coding RNA 2316 [Source:HGNC Symbol;Acc:HGNC:53235]"}, {"versioned_ensembl_gene_id":"ENSG00000273831.2","gene_symbol":"LRRC56","gene_name":"leucine rich repeat containing 56 [Source:HGNC Symbol;Acc:HGNC:25430]","synonyms":"FLJ00101,DKFZp761L1518","biotype":"protein_coding","ncbi_id":"115399","summary":null,"start":537527,"end":554915,"strand":1,"description":"leucine rich repeat containing 56 [Source:HGNC Symbol;Acc:HGNC:25430]"}, {"versioned_ensembl_gene_id":"ENSG00000223375.1","gene_symbol":"AC096638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":218338541,"end":218338756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156298.12","gene_symbol":"TSPAN7","gene_name":"tetraspanin 7 [Source:HGNC Symbol;Acc:HGNC:11854]","synonyms":"TM4SF2,TALLA-1,MXS1,MRX58,DXS1692E,CD231,A15","biotype":"protein_coding","ncbi_id":"7102","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked cognitive disability and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy. [provided by RefSeq, Jul 2008]","start":38561370,"end":38688920,"strand":1,"description":"tetraspanin 7 [Source:HGNC Symbol;Acc:HGNC:11854]"}, {"versioned_ensembl_gene_id":"ENSG00000259051.1","gene_symbol":"HNRNPUP1","gene_name":"heterogeneous nuclear ribonucleoprotein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19931]","synonyms":"HNRPUP","biotype":"processed_pseudogene","ncbi_id":"319134","summary":null,"start":43300263,"end":43300595,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein U pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19931]"}, {"versioned_ensembl_gene_id":"ENSG00000267060.5","gene_symbol":"PTGES3L","gene_name":"prostaglandin E synthase 3 like [Source:HGNC Symbol;Acc:HGNC:43943]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100885848","summary":null,"start":42968088,"end":42980433,"strand":-1,"description":"prostaglandin E synthase 3 like [Source:HGNC Symbol;Acc:HGNC:43943]"}, {"versioned_ensembl_gene_id":"ENSG00000105509.10","gene_symbol":"HAS1","gene_name":"hyaluronan synthase 1 [Source:HGNC Symbol;Acc:HGNC:4818]","synonyms":"HAS","biotype":"protein_coding","ncbi_id":"3036","summary":"Hyaluronan or hyaluronic acid (HA) is a high molecular weight unbranched polysaccharide synthesized by a wide variety of organisms from bacteria to mammals, and is a constituent of the extracellular matrix. It consists of alternating glucuronic acid and N-acetylglucosamine residues that are linked by beta-1-3 and beta-1-4 glycosidic bonds. HA is synthesized by membrane-bound synthase at the inner surface of the plasma membrane, and the chains are extruded through pore-like structures into the extracellular space. It serves a variety of functions, including space filling, lubrication of joints, and provision of a matrix through which cells can migrate. HA is actively produced during wound healing and tissue repair to provide a framework for ingrowth of blood vessels and fibroblasts. Changes in the serum concentration of HA are associated with inflammatory and degenerative arthropathies such as rheumatoid arthritis. In addition, the interaction of HA with the leukocyte receptor CD44 is important in tissue-specific homing by leukocytes, and overexpression of HA receptors has been correlated with tumor metastasis. HAS1 is a member of the newly identified vertebrate gene family encoding putative hyaluronan synthases, and its amino acid sequence shows significant homology to the hasA gene product of Streptococcus pyogenes, a glycosaminoglycan synthetase (DG42) from Xenopus laevis, and a recently described murine hyaluronan synthase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":51713112,"end":51723994,"strand":-1,"description":"hyaluronan synthase 1 [Source:HGNC Symbol;Acc:HGNC:4818]"}, {"versioned_ensembl_gene_id":"ENSG00000260579.1","gene_symbol":"AC024270.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83113617,"end":83114566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211841.1","gene_symbol":"TRAJ48","gene_name":"T-cell receptor alpha joining 48 [Source:HGNC Symbol;Acc:HGNC:12079]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28707","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22490491,"end":22490553,"strand":1,"description":"T-cell receptor alpha joining 48 [Source:HGNC Symbol;Acc:HGNC:12079]"}, {"versioned_ensembl_gene_id":"ENSG00000171931.12","gene_symbol":"FBXW10","gene_name":"F-box and WD repeat domain containing 10 [Source:HGNC Symbol;Acc:HGNC:1211]","synonyms":"SM2SH2,HREP,Fbw10,C17orf1A,C17orf1","biotype":"protein_coding","ncbi_id":"10517","summary":"Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":18744024,"end":18779349,"strand":1,"description":"F-box and WD repeat domain containing 10 [Source:HGNC Symbol;Acc:HGNC:1211]"}, {"versioned_ensembl_gene_id":"ENSG00000230967.2","gene_symbol":"AL133387.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101322485,"end":101323394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151553.14","gene_symbol":"FAM160B1","gene_name":"family with sequence similarity 160 member B1 [Source:HGNC Symbol;Acc:HGNC:29320]","synonyms":"KIAA1600,bA106M7.3","biotype":"protein_coding","ncbi_id":"57700","summary":null,"start":114821744,"end":114899832,"strand":1,"description":"family with sequence similarity 160 member B1 [Source:HGNC Symbol;Acc:HGNC:29320]"}, {"versioned_ensembl_gene_id":"ENSG00000224837.1","gene_symbol":"GCSHP5","gene_name":"glycine cleavage system protein H pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44195]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100329108","summary":null,"start":168055901,"end":168056422,"strand":-1,"description":"glycine cleavage system protein H pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44195]"}, {"versioned_ensembl_gene_id":"ENSG00000234070.1","gene_symbol":"SPATA17-AS1","gene_name":"SPATA17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41086]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103752555","summary":null,"start":217781198,"end":217785120,"strand":-1,"description":"SPATA17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41086]"}, {"versioned_ensembl_gene_id":"ENSG00000120314.18","gene_symbol":"WDR55","gene_name":"WD repeat domain 55 [Source:HGNC Symbol;Acc:HGNC:25971]","synonyms":"FLJ21702,FLJ20195","biotype":"protein_coding","ncbi_id":"54853","summary":null,"start":140664676,"end":140674124,"strand":1,"description":"WD repeat domain 55 [Source:HGNC Symbol;Acc:HGNC:25971]"}, {"versioned_ensembl_gene_id":"ENSG00000178860.8","gene_symbol":"MSC","gene_name":"musculin [Source:HGNC Symbol;Acc:HGNC:7321]","synonyms":"bHLHa22,ABF-1","biotype":"protein_coding","ncbi_id":"9242","summary":"The protein encoded by this gene is a transcriptional repressor capable of binding an E-box element either as a homodimer or as a heterodimer with E2A in vitro. The encoded protein also forms heterodimers with E2A proteins in vivo. This protein is capable of inhibiting the transactivation capability of E47, an E2A protein, in mammalian cells. This gene is a downstream target of the B-cell receptor signal transduction pathway. [provided by RefSeq, Jul 2008]","start":71841549,"end":71844468,"strand":-1,"description":"musculin [Source:HGNC Symbol;Acc:HGNC:7321]"}, {"versioned_ensembl_gene_id":"ENSG00000143158.10","gene_symbol":"MPC2","gene_name":"mitochondrial pyruvate carrier 2 [Source:HGNC Symbol;Acc:HGNC:24515]","synonyms":"SLC54A2,DKFZP564B167,BRP44","biotype":"protein_coding","ncbi_id":"25874","summary":null,"start":167916729,"end":167937040,"strand":-1,"description":"mitochondrial pyruvate carrier 2 [Source:HGNC Symbol;Acc:HGNC:24515]"}, {"versioned_ensembl_gene_id":"ENSG00000137948.18","gene_symbol":"BRDT","gene_name":"bromodomain testis associated [Source:HGNC Symbol;Acc:HGNC:1105]","synonyms":"CT9,BRD6","biotype":"protein_coding","ncbi_id":"676","summary":"BRDT is similar to the RING3 protein family. It possesses 2 bromodomain motifs and a PEST sequence (a cluster of proline, glutamic acid, serine, and threonine residues), characteristic of proteins that undergo rapid intracellular degradation. The bromodomain is found in proteins that regulate transcription. Several transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":91949371,"end":92014426,"strand":1,"description":"bromodomain testis associated [Source:HGNC Symbol;Acc:HGNC:1105]"}, {"versioned_ensembl_gene_id":"ENSG00000229821.1","gene_symbol":"AC103925.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201222113,"end":201223123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101955.14","gene_symbol":"SRPX","gene_name":"sushi repeat containing protein, X-linked [Source:HGNC Symbol;Acc:HGNC:11309]","synonyms":"ETX1","biotype":"protein_coding","ncbi_id":"8406","summary":null,"start":38149336,"end":38220924,"strand":-1,"description":"sushi repeat containing protein, X-linked [Source:HGNC Symbol;Acc:HGNC:11309]"}, {"versioned_ensembl_gene_id":"ENSG00000153498.11","gene_symbol":"SPACA7","gene_name":"sperm acrosome associated 7 [Source:HGNC Symbol;Acc:HGNC:29575]","synonyms":"C13orf28","biotype":"protein_coding","ncbi_id":"122258","summary":null,"start":112376319,"end":112434689,"strand":1,"description":"sperm acrosome associated 7 [Source:HGNC Symbol;Acc:HGNC:29575]"}, {"versioned_ensembl_gene_id":"ENSG00000233851.1","gene_symbol":"LATS2-AS1","gene_name":"LATS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39912]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874066","summary":null,"start":21005157,"end":21018122,"strand":1,"description":"LATS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39912]"}, {"versioned_ensembl_gene_id":"ENSG00000282203.1","gene_symbol":"TRBV7-3","gene_name":"T-cell receptor beta variable 7-3 [Source:HGNC Symbol;Acc:HGNC:12237]","synonyms":"TCRBV6S1A1N1,TRBV73,TCRBV7S3","biotype":"TR_V_gene","ncbi_id":"28595","summary":null,"start":142406045,"end":142406551,"strand":1,"description":"T-cell receptor beta variable 7-3 [Source:HGNC Symbol;Acc:HGNC:12237]"}, {"versioned_ensembl_gene_id":"ENSG00000258814.1","gene_symbol":"LINC02329","gene_name":"long intergenic non-protein coding RNA 2329 [Source:HGNC Symbol;Acc:HGNC:53249]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370605","summary":null,"start":85387275,"end":85388765,"strand":1,"description":"long intergenic non-protein coding RNA 2329 [Source:HGNC Symbol;Acc:HGNC:53249]"}, {"versioned_ensembl_gene_id":"ENSG00000055955.15","gene_symbol":"ITIH4","gene_name":"inter-alpha-trypsin inhibitor heavy chain family member 4 [Source:HGNC Symbol;Acc:HGNC:6169]","synonyms":"ITIHL1,IHRP,H4P","biotype":"protein_coding","ncbi_id":"3700","summary":"The protein encoded by this gene is secreted into the blood, where it is cleaved by plasma kallikrein into two smaller forms. Expression of this gene has been detected only in liver, and it seems to be upregulated during surgical trauma. This gene is part of a cluster of similar genes on chromosome 3. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":52812975,"end":52831479,"strand":-1,"description":"inter-alpha-trypsin inhibitor heavy chain family member 4 [Source:HGNC Symbol;Acc:HGNC:6169]"}, {"versioned_ensembl_gene_id":"ENSG00000284722.1","gene_symbol":"AP003175.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75069243,"end":75081023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236392.2","gene_symbol":"AC100848.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64147209,"end":64159299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227467.3","gene_symbol":"LINC01537","gene_name":"long intergenic non-protein coding RNA 1537 [Source:HGNC Symbol;Acc:HGNC:51301]","synonyms":"RP11-169D4.1-001","biotype":"lincRNA","ncbi_id":"101928555","summary":null,"start":72570660,"end":72573229,"strand":1,"description":"long intergenic non-protein coding RNA 1537 [Source:HGNC Symbol;Acc:HGNC:51301]"}, {"versioned_ensembl_gene_id":"ENSG00000239799.1","gene_symbol":"ITIH4-AS1","gene_name":"ITIH4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40310]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873993","summary":null,"start":52823935,"end":52825314,"strand":1,"description":"ITIH4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40310]"}, {"versioned_ensembl_gene_id":"ENSG00000266952.1","gene_symbol":"LINC01538","gene_name":"long intergenic non-protein coding RNA 1538 [Source:HGNC Symbol;Acc:HGNC:51306]","synonyms":"TCONS_00026184","biotype":"lincRNA","ncbi_id":"400654","summary":null,"start":64213082,"end":64260055,"strand":-1,"description":"long intergenic non-protein coding RNA 1538 [Source:HGNC Symbol;Acc:HGNC:51306]"}, {"versioned_ensembl_gene_id":"ENSG00000180336.17","gene_symbol":"MEIOC","gene_name":"meiosis specific with coiled-coil domain [Source:HGNC Symbol;Acc:HGNC:26670]","synonyms":"FLJ35848,C17orf104","biotype":"protein_coding","ncbi_id":"284071","summary":null,"start":44656404,"end":44690308,"strand":1,"description":"meiosis specific with coiled-coil domain [Source:HGNC Symbol;Acc:HGNC:26670]"}, {"versioned_ensembl_gene_id":"ENSG00000258636.1","gene_symbol":"AL121821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41587861,"end":41604856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267160.1","gene_symbol":"AC091152.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44673689,"end":44676257,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232143.9","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30586013,"end":30601810,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000236311.6","gene_symbol":"TLX1NB","gene_name":"TLX1 neighbor [Source:HGNC Symbol;Acc:HGNC:37183]","synonyms":"APT-B7,TDI,TD1","biotype":"processed_transcript","ncbi_id":"100038246","summary":null,"start":101089321,"end":101131126,"strand":-1,"description":"TLX1 neighbor [Source:HGNC Symbol;Acc:HGNC:37183]"}, {"versioned_ensembl_gene_id":"ENSG00000215374.5","gene_symbol":"FAM66B","gene_name":"family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128890","summary":null,"start":7301611,"end":7355354,"strand":-1,"description":"family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]"}, {"versioned_ensembl_gene_id":"ENSG00000245869.2","gene_symbol":"AP004609.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118885841,"end":118887742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011454.16","gene_symbol":"RABGAP1","gene_name":"RAB GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:17155]","synonyms":"TBC1D11,GAPCenA","biotype":"protein_coding","ncbi_id":"23637","summary":null,"start":122940833,"end":123104866,"strand":1,"description":"RAB GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:17155]"}, {"versioned_ensembl_gene_id":"ENSG00000223534.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480429","summary":null,"start":32659880,"end":32660729,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000100433.15","gene_symbol":"KCNK10","gene_name":"potassium two pore domain channel subfamily K member 10 [Source:HGNC Symbol;Acc:HGNC:6273]","synonyms":"TREK2,TREK-2,PPP1R97,K2p10.1","biotype":"protein_coding","ncbi_id":"54207","summary":"The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations, and is stimulated strongly by arachidonic acid and to a lesser degree by membrane stretching, intracellular acidification, and general anaesthetics. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008]","start":88180103,"end":88326907,"strand":-1,"description":"potassium two pore domain channel subfamily K member 10 [Source:HGNC Symbol;Acc:HGNC:6273]"}, {"versioned_ensembl_gene_id":"ENSG00000158023.9","gene_symbol":"WDR66","gene_name":"WD repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:28506]","synonyms":"MGC33630,CaM-IP4","biotype":"protein_coding","ncbi_id":"144406","summary":"This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member appears to function in the determination of mean platelet volume (MPV), and polymorphisms in this gene have been associated with variance in MPV. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":121917862,"end":122003927,"strand":1,"description":"WD repeat domain 66 [Source:HGNC Symbol;Acc:HGNC:28506]"}, {"versioned_ensembl_gene_id":"ENSG00000256950.2","gene_symbol":"AC069503.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":121888809,"end":121921470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112983.17","gene_symbol":"BRD8","gene_name":"bromodomain containing 8 [Source:HGNC Symbol;Acc:HGNC:19874]","synonyms":"SMAP,p120","biotype":"protein_coding","ncbi_id":"10902","summary":"The protein encoded by this gene interacts with thyroid hormone receptor in a ligand-dependent manner and enhances thyroid hormone-dependent activation from thyroid response elements. This protein contains a bromodomain and is thought to be a nuclear receptor coactivator. Multiple alternatively spliced transcript variants that encode distinct isoforms have been identified. [provided by RefSeq, Jul 2014]","start":138139766,"end":138178986,"strand":-1,"description":"bromodomain containing 8 [Source:HGNC Symbol;Acc:HGNC:19874]"}, {"versioned_ensembl_gene_id":"ENSG00000108551.4","gene_symbol":"RASD1","gene_name":"ras related dexamethasone induced 1 [Source:HGNC Symbol;Acc:HGNC:15828]","synonyms":"DEXRAS1,AGS1","biotype":"protein_coding","ncbi_id":"51655","summary":"This gene encodes a member of the Ras superfamily of small GTPases and is induced by dexamethasone. The encoded protein is an activator of G-protein signaling and acts as a direct nucleotide exchange factor for Gi-Go proteins. This protein interacts with the neuronal nitric oxide adaptor protein CAPON, and a nuclear adaptor protein FE65, which interacts with the Alzheimer's disease amyloid precursor protein. This gene may play a role in dexamethasone-induced alterations in cell morphology, growth and cell-extracellular matrix interactions. Epigenetic inactivation of this gene is closely correlated with resistance to dexamethasone in multiple myeloma cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2011]","start":17494437,"end":17496395,"strand":-1,"description":"ras related dexamethasone induced 1 [Source:HGNC Symbol;Acc:HGNC:15828]"}, {"versioned_ensembl_gene_id":"ENSG00000259909.1","gene_symbol":"AC100827.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72638821,"end":72640125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271028.1","gene_symbol":"AC009643.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43063637,"end":43065932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254725.1","gene_symbol":"AC009643.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43065686,"end":43066076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282515.1","gene_symbol":"AC242019.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1247928,"end":1260201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249456.1","gene_symbol":"AL731577.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":124917143,"end":124942881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227852.1","gene_symbol":"RPS29P17","gene_name":"ribosomal protein S29 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35479]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129379","summary":null,"start":35592786,"end":35592951,"strand":1,"description":"ribosomal protein S29 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35479]"}, {"versioned_ensembl_gene_id":"ENSG00000273038.2","gene_symbol":"AL365203.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32887255,"end":32889311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228901.3","gene_symbol":"HMGN2P36","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39407]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874480","summary":null,"start":13610363,"end":13610771,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:39407]"}, {"versioned_ensembl_gene_id":"ENSG00000267952.1","gene_symbol":"AC008878.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7507052,"end":7519622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254604.1","gene_symbol":"AP002336.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70282367,"end":70363368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276175.4","gene_symbol":"LILRA3","gene_name":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]","synonyms":"ILT6,HM43,HM31,LIR4,CD85e,LIR-4","biotype":"protein_coding","ncbi_id":"11026","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]","start":54294163,"end":54306461,"strand":-1,"description":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]"}, {"versioned_ensembl_gene_id":"ENSG00000130827.6","gene_symbol":"PLXNA3","gene_name":"plexin A3 [Source:HGNC Symbol;Acc:HGNC:9101]","synonyms":"XAP-6,SEX,PLXN4,Plxn3,6.3","biotype":"protein_coding","ncbi_id":"55558","summary":"This gene encodes a member of the plexin class of proteins. The encoded protein is a class 3 semaphorin receptor, and may be involved in cytoskeletal remodeling and as well as apoptosis. Studies of a similar gene in zebrafish suggest that it is important for axon pathfinding in the developing nervous system. This gene may be associated with tumor progression. [provided by RefSeq, Aug 2013]","start":154458281,"end":154477779,"strand":1,"description":"plexin A3 [Source:HGNC Symbol;Acc:HGNC:9101]"}, {"versioned_ensembl_gene_id":"ENSG00000226983.2","gene_symbol":"LINC01692","gene_name":"long intergenic non-protein coding RNA 1692 [Source:HGNC Symbol;Acc:HGNC:52480]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339622","summary":null,"start":24840550,"end":25057746,"strand":1,"description":"long intergenic non-protein coding RNA 1692 [Source:HGNC Symbol;Acc:HGNC:52480]"}, {"versioned_ensembl_gene_id":"ENSG00000175224.16","gene_symbol":"ATG13","gene_name":"autophagy related 13 [Source:HGNC Symbol;Acc:HGNC:29091]","synonyms":"KIAA0652","biotype":"protein_coding","ncbi_id":"9776","summary":"The protein encoded by this gene is an autophagy factor and a target of the TOR kinase signaling pathway. The encoded protein is essential for autophagosome formation and mitophagy. [provided by RefSeq, Oct 2016]","start":46617527,"end":46674818,"strand":1,"description":"autophagy related 13 [Source:HGNC Symbol;Acc:HGNC:29091]"}, {"versioned_ensembl_gene_id":"ENSG00000233270.1","gene_symbol":"SNRPEP4","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43446]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130109","summary":null,"start":5576660,"end":5576938,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43446]"}, {"versioned_ensembl_gene_id":"ENSG00000211825.1","gene_symbol":"TRDJ1","gene_name":"T-cell receptor delta joining 1 [Source:HGNC Symbol;Acc:HGNC:12257]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28522","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22450089,"end":22450139,"strand":1,"description":"T-cell receptor delta joining 1 [Source:HGNC Symbol;Acc:HGNC:12257]"}, {"versioned_ensembl_gene_id":"ENSG00000237484.5","gene_symbol":"LINC01684","gene_name":"long intergenic non-protein coding RNA 1684 [Source:HGNC Symbol;Acc:HGNC:52472]","synonyms":"lnc-JAM2-6","biotype":"lincRNA","ncbi_id":"105372751","summary":null,"start":24428740,"end":24547942,"strand":1,"description":"long intergenic non-protein coding RNA 1684 [Source:HGNC Symbol;Acc:HGNC:52472]"}, {"versioned_ensembl_gene_id":"ENSG00000278084.1","gene_symbol":"AC069503.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121874193,"end":121874337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142235.8","gene_symbol":"LMTK3","gene_name":"lemur tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:19295]","synonyms":"TYKLM3,PPP1R101,LMR3,KIAA1883","biotype":"protein_coding","ncbi_id":"114783","summary":null,"start":48485271,"end":48513189,"strand":-1,"description":"lemur tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:19295]"}, {"versioned_ensembl_gene_id":"ENSG00000249847.1","gene_symbol":"AC104619.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134932889,"end":134934131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243469.1","gene_symbol":"RPL7P51","gene_name":"ribosomal protein L7 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36432]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271226","summary":null,"start":51648862,"end":51649610,"strand":1,"description":"ribosomal protein L7 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36432]"}, {"versioned_ensembl_gene_id":"ENSG00000256128.5","gene_symbol":"LINC00944","gene_name":"long intergenic non-protein coding RNA 944 [Source:HGNC Symbol;Acc:HGNC:48640]","synonyms":null,"biotype":"lincRNA","ncbi_id":"387895","summary":null,"start":126729787,"end":126772411,"strand":-1,"description":"long intergenic non-protein coding RNA 944 [Source:HGNC Symbol;Acc:HGNC:48640]"}, {"versioned_ensembl_gene_id":"ENSG00000249000.1","gene_symbol":"AC093722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134759399,"end":134817289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279769.1","gene_symbol":"CU639417.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6034690,"end":6036093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254668.1","gene_symbol":"AC023442.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41797543,"end":41797964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006432.15","gene_symbol":"MAP3K9","gene_name":"mitogen-activated protein kinase kinase kinase 9 [Source:HGNC Symbol;Acc:HGNC:6861]","synonyms":"PRKE1,MLK1,MEKK9","biotype":"protein_coding","ncbi_id":"4293","summary":null,"start":70722526,"end":70809534,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 9 [Source:HGNC Symbol;Acc:HGNC:6861]"}, {"versioned_ensembl_gene_id":"ENSG00000248174.5","gene_symbol":"LINC02268","gene_name":"long intergenic non-protein coding RNA 2268 [Source:HGNC Symbol;Acc:HGNC:53183]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928509","summary":null,"start":174094660,"end":174220398,"strand":-1,"description":"long intergenic non-protein coding RNA 2268 [Source:HGNC Symbol;Acc:HGNC:53183]"}, {"versioned_ensembl_gene_id":"ENSG00000282029.1","gene_symbol":"AC120035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1160740,"end":1186922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237859.2","gene_symbol":"EEF1A1P31","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37908]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"553820","summary":null,"start":154908885,"end":154919103,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37908]"}, {"versioned_ensembl_gene_id":"ENSG00000241357.1","gene_symbol":"AC092849.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100435257,"end":100436510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241112.1","gene_symbol":"RPL29P14","gene_name":"ribosomal protein L29 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36687]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270974","summary":null,"start":149545383,"end":149545810,"strand":-1,"description":"ribosomal protein L29 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36687]"}, {"versioned_ensembl_gene_id":"ENSG00000187051.8","gene_symbol":"RPS19BP1","gene_name":"ribosomal protein S19 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:28749]","synonyms":"FLJ21770,MGC52010","biotype":"protein_coding","ncbi_id":"91582","summary":null,"start":39529093,"end":39532855,"strand":-1,"description":"ribosomal protein S19 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:28749]"}, {"versioned_ensembl_gene_id":"ENSG00000236019.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31524481,"end":31525315,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000100445.17","gene_symbol":"SDR39U1","gene_name":"short chain dehydrogenase/reductase family 39U member 1 [Source:HGNC Symbol;Acc:HGNC:20275]","synonyms":"HCDI,C14orf124","biotype":"protein_coding","ncbi_id":"56948","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) superfamily, which includes both classical and extended types. The encoded protein represents an extended type, with similarity to epimerases. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Mar 2014]","start":24439766,"end":24442905,"strand":-1,"description":"short chain dehydrogenase/reductase family 39U member 1 [Source:HGNC Symbol;Acc:HGNC:20275]"}, {"versioned_ensembl_gene_id":"ENSG00000243023.2","gene_symbol":"UBA52P3","gene_name":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122837","summary":null,"start":58141279,"end":58141660,"strand":1,"description":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20056]"}, {"versioned_ensembl_gene_id":"ENSG00000243314.1","gene_symbol":"AC106707.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158496561,"end":158496934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279822.1","gene_symbol":"AC016397.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48443836,"end":48445820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074356.16","gene_symbol":"NCBP3","gene_name":"nuclear cap binding subunit 3 [Source:HGNC Symbol;Acc:HGNC:24612]","synonyms":"HSA277841,ELG,C17orf85","biotype":"protein_coding","ncbi_id":"55421","summary":null,"start":3802165,"end":3846251,"strand":-1,"description":"nuclear cap binding subunit 3 [Source:HGNC Symbol;Acc:HGNC:24612]"}, {"versioned_ensembl_gene_id":"ENSG00000136883.13","gene_symbol":"KIF12","gene_name":"kinesin family member 12 [Source:HGNC Symbol;Acc:HGNC:21495]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113220","summary":"This gene encodes a member of the kinesin superfamily of microtubule-associated molecular motors with functions related to the microtubule cytosekelton. Members of this superfamily play important roles in intracellular transport and cell division. A similar protein in mouse functions in the beta cell antioxidant signaling cascade, acting as a scaffold for the transcription factor specificity protein 1 (Sp1). Mice that lack this gene exhibit beta cell oxidative stress resulting in hypoinsulinemic glucose intolerance. [provided by RefSeq, Jul 2016]","start":114086126,"end":114099291,"strand":-1,"description":"kinesin family member 12 [Source:HGNC Symbol;Acc:HGNC:21495]"}, {"versioned_ensembl_gene_id":"ENSG00000255944.1","gene_symbol":"AC006065.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126628172,"end":126690322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255900.1","gene_symbol":"AC006065.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126616344,"end":126616554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278376.1","gene_symbol":"AP004609.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118791254,"end":118793137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256732.1","gene_symbol":"AC006065.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126610034,"end":126690318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057019.15","gene_symbol":"DCBLD2","gene_name":"discoidin, CUB and LCCL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24627]","synonyms":"ESDN,CLCP1","biotype":"protein_coding","ncbi_id":"131566","summary":null,"start":98795941,"end":98901689,"strand":-1,"description":"discoidin, CUB and LCCL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24627]"}, {"versioned_ensembl_gene_id":"ENSG00000256310.1","gene_symbol":"NDUFA5P6","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48848]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288339","summary":null,"start":126524248,"end":126524626,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48848]"}, {"versioned_ensembl_gene_id":"ENSG00000267417.1","gene_symbol":"AC138474.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13013662,"end":13014511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173085.13","gene_symbol":"COQ2","gene_name":"coenzyme Q2, polyprenyltransferase [Source:HGNC Symbol;Acc:HGNC:25223]","synonyms":"FLJ26072,CL640","biotype":"protein_coding","ncbi_id":"27235","summary":"This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009]","start":83261536,"end":83284914,"strand":-1,"description":"coenzyme Q2, polyprenyltransferase [Source:HGNC Symbol;Acc:HGNC:25223]"}, {"versioned_ensembl_gene_id":"ENSG00000100441.9","gene_symbol":"KHNYN","gene_name":"KH and NYN domain containing [Source:HGNC Symbol;Acc:HGNC:20166]","synonyms":"KIAA0323","biotype":"protein_coding","ncbi_id":"23351","summary":"This gene encodes a protein containing a ribonuclease NYN domain. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":24429286,"end":24441834,"strand":1,"description":"KH and NYN domain containing [Source:HGNC Symbol;Acc:HGNC:20166]"}, {"versioned_ensembl_gene_id":"ENSG00000126581.12","gene_symbol":"BECN1","gene_name":"beclin 1 [Source:HGNC Symbol;Acc:HGNC:1034]","synonyms":"VPS30,ATG6","biotype":"protein_coding","ncbi_id":"8678","summary":"This gene encodes a protein that regulates autophagy, a catabolic process of degradation induced by starvation. The encoded protein is a component of the phosphatidylinositol-3-kinase (PI3K) complex which mediates vesicle-trafficking processes. This protein is thought to play a role in multiple cellular processes, including tumorigenesis, neurodegeneration and apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42810134,"end":42833350,"strand":-1,"description":"beclin 1 [Source:HGNC Symbol;Acc:HGNC:1034]"}, {"versioned_ensembl_gene_id":"ENSG00000184270.4","gene_symbol":"HIST2H2AB","gene_name":"histone cluster 2 H2A family member b [Source:HGNC Symbol;Acc:HGNC:20508]","synonyms":null,"biotype":"protein_coding","ncbi_id":"317772","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":149887524,"end":149887916,"strand":-1,"description":"histone cluster 2 H2A family member b [Source:HGNC Symbol;Acc:HGNC:20508]"}, {"versioned_ensembl_gene_id":"ENSG00000143199.17","gene_symbol":"ADCY10","gene_name":"adenylate cyclase 10, soluble [Source:HGNC Symbol;Acc:HGNC:21285]","synonyms":"SAC,RP1-313L4.2,HCA2,Sacy,SACI","biotype":"protein_coding","ncbi_id":"55811","summary":"The protein encoded by this gene belongs to a distinct class of adenylyl cyclases that is soluble and insensitive to G protein or forskolin regulation. Activity of this protein is regulated by bicarbonate. Variation at this gene has been observed in patients with absorptive hypercalciuria. Alternatively spliced transcript variants encoding different isoforms have been observed. There is a pseudogene of this gene on chromosome 6. [provided by RefSeq, Jul 2014]","start":167809388,"end":167914215,"strand":-1,"description":"adenylate cyclase 10, soluble [Source:HGNC Symbol;Acc:HGNC:21285]"}, {"versioned_ensembl_gene_id":"ENSG00000268500.5","gene_symbol":"AC018755.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":51612091,"end":51646889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089057.14","gene_symbol":"SLC23A2","gene_name":"solute carrier family 23 member 2 [Source:HGNC Symbol;Acc:HGNC:10973]","synonyms":"YSPL2,SVCT2,SLC23A1,KIAA0238","biotype":"protein_coding","ncbi_id":"9962","summary":"The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1. [provided by RefSeq, Jul 2008]","start":4852356,"end":5010293,"strand":-1,"description":"solute carrier family 23 member 2 [Source:HGNC Symbol;Acc:HGNC:10973]"}, {"versioned_ensembl_gene_id":"ENSG00000230551.4","gene_symbol":"AC021078.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":149494314,"end":149504670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232087.1","gene_symbol":"HCFC2P1","gene_name":"host cell factor C2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39815]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419149","summary":null,"start":108480226,"end":108481817,"strand":1,"description":"host cell factor C2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39815]"}, {"versioned_ensembl_gene_id":"ENSG00000065485.19","gene_symbol":"PDIA5","gene_name":"protein disulfide isomerase family A member 5 [Source:HGNC Symbol;Acc:HGNC:24811]","synonyms":"PDIR,FLJ30401","biotype":"protein_coding","ncbi_id":"10954","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, three catalytically active thioredoxin (TRX) domains, a TRX-like domain, and a C-terminal ER-retention sequence. The N-terminal TRX-like domain is the primary binding site for the major ER chaperone calreticulin and possibly other proteins and substrates as well. Alternative splicing results in multiple protein- and non-protein-coding transcript variants. [provided by RefSeq, Dec 2016]","start":123067062,"end":123225227,"strand":1,"description":"protein disulfide isomerase family A member 5 [Source:HGNC Symbol;Acc:HGNC:24811]"}, {"versioned_ensembl_gene_id":"ENSG00000244342.5","gene_symbol":"LINC00698","gene_name":"long intergenic non-protein coding RNA 698 [Source:HGNC Symbol;Acc:HGNC:27720]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285401","summary":null,"start":62950430,"end":63125062,"strand":1,"description":"long intergenic non-protein coding RNA 698 [Source:HGNC Symbol;Acc:HGNC:27720]"}, {"versioned_ensembl_gene_id":"ENSG00000237064.1","gene_symbol":"EIF3IP1","gene_name":"eukaryotic translation initiation factor 3 subunit I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13277]","synonyms":"RG208K23","biotype":"processed_pseudogene","ncbi_id":"442720","summary":null,"start":109959218,"end":109960184,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13277]"}, {"versioned_ensembl_gene_id":"ENSG00000283384.1","gene_symbol":"AL138694.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":108335354,"end":108448316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226082.2","gene_symbol":"AC096915.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62926371,"end":62926882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203392.3","gene_symbol":"AC105020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75678548,"end":75680752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236422.1","gene_symbol":"BX927214.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30403920,"end":30404553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185010.13","gene_symbol":"F8","gene_name":"coagulation factor VIII [Source:HGNC Symbol;Acc:HGNC:3546]","synonyms":"HEMA,FVIII,F8C,DXS1253E","biotype":"protein_coding","ncbi_id":"2157","summary":"This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder. [provided by RefSeq, Jul 2008]","start":154835788,"end":155026940,"strand":-1,"description":"coagulation factor VIII [Source:HGNC Symbol;Acc:HGNC:3546]"}, {"versioned_ensembl_gene_id":"ENSG00000279636.2","gene_symbol":"LINC00216","gene_name":"long intergenic non-protein coding RNA 216 [Source:NCBI gene;Acc:55451]","synonyms":"PRO1617,NCRNA00216,C14orf107","biotype":"lincRNA","ncbi_id":"55451","summary":null,"start":58288033,"end":58289158,"strand":1,"description":"long intergenic non-protein coding RNA 216 [Source:NCBI gene;Acc:55451]"}, {"versioned_ensembl_gene_id":"ENSG00000132323.8","gene_symbol":"ILKAP","gene_name":"ILK associated serine/threonine phosphatase [Source:HGNC Symbol;Acc:HGNC:15566]","synonyms":"PPM1O,FLJ10181,DKFZP434J2031","biotype":"protein_coding","ncbi_id":"80895","summary":"The protein encoded by this gene is a protein serine/threonine phosphatase of the PP2C family. This protein can interact with integrin-linked kinase (ILK/ILK1), a regulator of integrin mediated signaling, and regulate the kinase activity of ILK. Through the interaction with ILK, this protein may selectively affect the signaling process of ILK-mediated glycogen synthase kinase 3 beta (GSK3beta), and thus participate in Wnt signaling pathway. [provided by RefSeq, Jul 2008]","start":238170401,"end":238203729,"strand":-1,"description":"ILK associated serine/threonine phosphatase [Source:HGNC Symbol;Acc:HGNC:15566]"}, {"versioned_ensembl_gene_id":"ENSG00000186594.14","gene_symbol":"MIR22HG","gene_name":"MIR22 host gene [Source:HGNC Symbol;Acc:HGNC:28219]","synonyms":"MGC14376,DKFZp686O06159,C17orf91","biotype":"lincRNA","ncbi_id":"84981","summary":null,"start":1711493,"end":1717174,"strand":-1,"description":"MIR22 host gene [Source:HGNC Symbol;Acc:HGNC:28219]"}, {"versioned_ensembl_gene_id":"ENSG00000257053.1","gene_symbol":"Z98941.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121149010,"end":121149109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253434.5","gene_symbol":"LINC02237","gene_name":"long intergenic non-protein coding RNA 2237 [Source:HGNC Symbol;Acc:HGNC:53108]","synonyms":"RP11-1101K5.1","biotype":"lincRNA","ncbi_id":"105375706","summary":null,"start":111376639,"end":111542973,"strand":1,"description":"long intergenic non-protein coding RNA 2237 [Source:HGNC Symbol;Acc:HGNC:53108]"}, {"versioned_ensembl_gene_id":"ENSG00000121542.11","gene_symbol":"SEC22A","gene_name":"SEC22 homolog A, vesicle trafficking protein [Source:HGNC Symbol;Acc:HGNC:20260]","synonyms":"SEC22L2","biotype":"protein_coding","ncbi_id":"26984","summary":"The protein encoded by this gene belongs to the member of the SEC22 family of vesicle trafficking proteins. This protein has similarity to rat SEC22 and may act in the early stages of the secretory pathway. [provided by RefSeq, Nov 2008]","start":123201927,"end":123274130,"strand":1,"description":"SEC22 homolog A, vesicle trafficking protein [Source:HGNC Symbol;Acc:HGNC:20260]"}, {"versioned_ensembl_gene_id":"ENSG00000274183.1","gene_symbol":"H2AFB1","gene_name":"H2A histone family member B1 [Source:HGNC Symbol;Acc:HGNC:22516]","synonyms":null,"biotype":"protein_coding","ncbi_id":"474382","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the most centromeric copy which is in intron 22 of the F8 gene. [provided by RefSeq, Oct 2015]","start":154884972,"end":154885558,"strand":1,"description":"H2A histone family member B1 [Source:HGNC Symbol;Acc:HGNC:22516]"}, {"versioned_ensembl_gene_id":"ENSG00000227968.1","gene_symbol":"BUB3P1","gene_name":"BUB3 mitotic checkpoint protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51559]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646614","summary":null,"start":108994031,"end":108995029,"strand":-1,"description":"BUB3 mitotic checkpoint protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51559]"}, {"versioned_ensembl_gene_id":"ENSG00000139971.15","gene_symbol":"C14orf37","gene_name":"chromosome 14 open reading frame 37 [Source:HGNC Symbol;Acc:HGNC:19846]","synonyms":"UT2","biotype":"protein_coding","ncbi_id":"145407","summary":null,"start":57999735,"end":58298139,"strand":-1,"description":"chromosome 14 open reading frame 37 [Source:HGNC Symbol;Acc:HGNC:19846]"}, {"versioned_ensembl_gene_id":"ENSG00000160111.12","gene_symbol":"CPAMD8","gene_name":"C3 and PZP like, alpha-2-macroglobulin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23228]","synonyms":"VIP,KIAA1283,K-CAP","biotype":"protein_coding","ncbi_id":"27151","summary":"This gene encodes a member of the protease inhibitor I39 (alpha-2-macroglobulin) family of proteins. These proteins are important in innate and acquired immunity. The encoded protein is membrane-associated and proteolytically processed to generate two chains. Mutations in this gene cause a form of anterior segment dysgenesis, a developmental disorder of the eye. [provided by RefSeq, May 2017]","start":16892947,"end":17026815,"strand":-1,"description":"C3 and PZP like, alpha-2-macroglobulin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:23228]"}, {"versioned_ensembl_gene_id":"ENSG00000205174.4","gene_symbol":"C7orf66","gene_name":"chromosome 7 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33712]","synonyms":null,"biotype":"lincRNA","ncbi_id":"154907","summary":null,"start":108883975,"end":108884587,"strand":-1,"description":"chromosome 7 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33712]"}, {"versioned_ensembl_gene_id":"ENSG00000270425.1","gene_symbol":"AC002487.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108720608,"end":108721601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277246.1","gene_symbol":"AL157762.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":108267320,"end":108267734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214359.3","gene_symbol":"RPL18P10","gene_name":"ribosomal protein L18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35957]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271286","summary":null,"start":50099331,"end":50099868,"strand":1,"description":"ribosomal protein L18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35957]"}, {"versioned_ensembl_gene_id":"ENSG00000237152.3","gene_symbol":"DLEU7-AS1","gene_name":"DLEU7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39966]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874074","summary":null,"start":50807856,"end":50849905,"strand":1,"description":"DLEU7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39966]"}, {"versioned_ensembl_gene_id":"ENSG00000260867.1","gene_symbol":"AC009107.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58197112,"end":58217805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282293.1","gene_symbol":"AC245078.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11048621,"end":11049550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229391.7","gene_symbol":"HLA-DRB6","gene_name":"major histocompatibility complex, class II, DR beta 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4954]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3128","summary":null,"start":32552713,"end":32560022,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4954]"}, {"versioned_ensembl_gene_id":"ENSG00000282594.1","gene_symbol":"LINC01300","gene_name":"long intergenic non-protein coding RNA 1300 [Source:HGNC Symbol;Acc:HGNC:50460]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"731779","summary":null,"start":141340549,"end":141344621,"strand":1,"description":"long intergenic non-protein coding RNA 1300 [Source:HGNC Symbol;Acc:HGNC:50460]"}, {"versioned_ensembl_gene_id":"ENSG00000128052.8","gene_symbol":"KDR","gene_name":"kinase insert domain receptor [Source:HGNC Symbol;Acc:HGNC:6307]","synonyms":"FLK1,CD309,VEGFR2,VEGFR","biotype":"protein_coding","ncbi_id":"3791","summary":"Vascular endothelial growth factor (VEGF) is a major growth factor for endothelial cells. This gene encodes one of the two receptors of the VEGF. This receptor, known as kinase insert domain receptor, is a type III receptor tyrosine kinase. It functions as the main mediator of VEGF-induced endothelial proliferation, survival, migration, tubular morphogenesis and sprouting. The signalling and trafficking of this receptor are regulated by multiple factors, including Rab GTPase, P2Y purine nucleotide receptor, integrin alphaVbeta3, T-cell protein tyrosine phosphatase, etc.. Mutations of this gene are implicated in infantile capillary hemangiomas. [provided by RefSeq, May 2009]","start":55078477,"end":55125589,"strand":-1,"description":"kinase insert domain receptor [Source:HGNC Symbol;Acc:HGNC:6307]"}, {"versioned_ensembl_gene_id":"ENSG00000250646.1","gene_symbol":"AC111194.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55053060,"end":55092534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102524.11","gene_symbol":"TNFSF13B","gene_name":"TNF superfamily member 13b [Source:HGNC Symbol;Acc:HGNC:11929]","synonyms":"TNFSF20,THANK,TALL1,TALL-1,CD257,BLYS,BAFF","biotype":"protein_coding","ncbi_id":"10673","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for receptors TNFRSF13B/TACI, TNFRSF17/BCMA, and TNFRSF13C/BAFFR. This cytokine is expressed in B cell lineage cells, and acts as a potent B cell activator. It has been also shown to play an important role in the proliferation and differentiation of B cells. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011]","start":108251240,"end":108308484,"strand":1,"description":"TNF superfamily member 13b [Source:HGNC Symbol;Acc:HGNC:11929]"}, {"versioned_ensembl_gene_id":"ENSG00000184678.10","gene_symbol":"HIST2H2BE","gene_name":"histone cluster 2 H2B family member e [Source:HGNC Symbol;Acc:HGNC:4760]","synonyms":"H2BFQ,H2B/q,H2B.1,H2B","biotype":"protein_coding","ncbi_id":"8349","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-dependent histone that is a member of the histone H2B family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif. The protein has antibacterial and antifungal antimicrobial activity. [provided by RefSeq, Aug 2015]","start":149884459,"end":149886652,"strand":-1,"description":"histone cluster 2 H2B family member e [Source:HGNC Symbol;Acc:HGNC:4760]"}, {"versioned_ensembl_gene_id":"ENSG00000260927.1","gene_symbol":"AC009107.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58129529,"end":58159133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248317.1","gene_symbol":"AC111194.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54943630,"end":54956818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212695.5","gene_symbol":"AL583805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8713311,"end":8713841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265205.1","gene_symbol":"AC010761.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28670054,"end":28672804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235389.2","gene_symbol":"AL583805.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8700595,"end":8701552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197081.12","gene_symbol":"IGF2R","gene_name":"insulin like growth factor 2 receptor [Source:HGNC Symbol;Acc:HGNC:5467]","synonyms":"CIMPR,CI-MPR,CI-M6PR,CD222,MPRI,MPR300,MPR1,M6P-R","biotype":"protein_coding","ncbi_id":"3482","summary":"This gene encodes a receptor for both insulin-like growth factor 2 and mannose 6-phosphate. The binding sites for each ligand are located on different segments of the protein. This receptor has various functions, including in the intracellular trafficking of lysosomal enzymes, the activation of transforming growth factor beta, and the degradation of insulin-like growth factor 2. Mutation or loss of heterozygosity of this gene has been association with risk of hepatocellular carcinoma. The orthologous mouse gene is imprinted and shows exclusive expression from the maternal allele; however, imprinting of the human gene may be polymorphic, as only a minority of individuals showed biased expression from the maternal allele (PMID:8267611). [provided by RefSeq, Nov 2015]","start":159969099,"end":160113507,"strand":1,"description":"insulin like growth factor 2 receptor [Source:HGNC Symbol;Acc:HGNC:5467]"}, {"versioned_ensembl_gene_id":"ENSG00000225647.1","gene_symbol":"AC005487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108598375,"end":108614267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281930.1","gene_symbol":"SMIM10L1","gene_name":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129361","summary":null,"start":11167456,"end":11172249,"strand":1,"description":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]"}, {"versioned_ensembl_gene_id":"ENSG00000269130.1","gene_symbol":"AC020914.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51560122,"end":51560590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282174.1","gene_symbol":"AC006518.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10831074,"end":10832016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238289.9","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31574447,"end":31587478,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000276541.2","gene_symbol":"TAS2R14","gene_name":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]","synonyms":"TRB1,T2R14","biotype":"protein_coding","ncbi_id":"50840","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10937405,"end":11167807,"strand":-1,"description":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]"}, {"versioned_ensembl_gene_id":"ENSG00000170903.10","gene_symbol":"MSANTD4","gene_name":"Myb/SANT DNA binding domain containing 4 with coiled-coils [Source:HGNC Symbol;Acc:HGNC:29383]","synonyms":"KIAA1826","biotype":"protein_coding","ncbi_id":"84437","summary":null,"start":105995623,"end":106022403,"strand":-1,"description":"Myb/SANT DNA binding domain containing 4 with coiled-coils [Source:HGNC Symbol;Acc:HGNC:29383]"}, {"versioned_ensembl_gene_id":"ENSG00000276167.1","gene_symbol":"TAS2R50","gene_name":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]","synonyms":"T2R51","biotype":"protein_coding","ncbi_id":"259296","summary":"TAS2R50 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). See also TAS2R10 (MIM 604791).[supplied by OMIM, Mar 2008]","start":10985900,"end":10986899,"strand":-1,"description":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]"}, {"versioned_ensembl_gene_id":"ENSG00000282079.1","gene_symbol":"AC245078.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11079729,"end":11080651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104415.13","gene_symbol":"WISP1","gene_name":"WNT1 inducible signaling pathway protein 1 [Source:HGNC Symbol;Acc:HGNC:12769]","synonyms":"CCN4","biotype":"protein_coding","ncbi_id":"8840","summary":"This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. It is expressed at a high level in fibroblast cells, and overexpressed in colon tumors. The encoded protein binds to decorin and biglycan, two members of a family of small leucine-rich proteoglycans present in the extracellular matrix of connective tissue, and possibly prevents the inhibitory activity of decorin and biglycan in tumor cell proliferation. It also attenuates p53-mediated apoptosis in response to DNA damage through activation of the Akt kinase. It is 83% identical to the mouse protein at the amino acid level. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2011]","start":133191039,"end":133230344,"strand":1,"description":"WNT1 inducible signaling pathway protein 1 [Source:HGNC Symbol;Acc:HGNC:12769]"}, {"versioned_ensembl_gene_id":"ENSG00000251256.1","gene_symbol":"LINC02358","gene_name":"long intergenic non-protein coding RNA 2358 [Source:HGNC Symbol;Acc:HGNC:53281]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986226","summary":null,"start":54845568,"end":54859241,"strand":1,"description":"long intergenic non-protein coding RNA 2358 [Source:HGNC Symbol;Acc:HGNC:53281]"}, {"versioned_ensembl_gene_id":"ENSG00000275679.4","gene_symbol":"PRH2","gene_name":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]","synonyms":"Pr","biotype":"protein_coding","ncbi_id":"5555","summary":"This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. In western population this locus is commonly biallelic and encodes proline-rich protein (PRP) isoforms, PRP-1 and PRP-2. The reference genome encodes the PRP-1 allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Oct 2015]","start":10929236,"end":10932341,"strand":1,"description":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]"}, {"versioned_ensembl_gene_id":"ENSG00000271093.1","gene_symbol":"IGLCOR22-2","gene_name":"immunoglobulin lambda constant/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15697]","synonyms":"IGLC/OR22-2","biotype":"IG_C_pseudogene","ncbi_id":"84086","summary":null,"start":32356676,"end":32356988,"strand":-1,"description":"immunoglobulin lambda constant/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15697]"}, {"versioned_ensembl_gene_id":"ENSG00000185361.8","gene_symbol":"TNFAIP8L1","gene_name":"TNF alpha induced protein 8 like 1 [Source:HGNC Symbol;Acc:HGNC:28279]","synonyms":"MGC17791","biotype":"protein_coding","ncbi_id":"126282","summary":null,"start":4639518,"end":4655568,"strand":1,"description":"TNF alpha induced protein 8 like 1 [Source:HGNC Symbol;Acc:HGNC:28279]"}, {"versioned_ensembl_gene_id":"ENSG00000130023.15","gene_symbol":"ERMARD","gene_name":"ER membrane associated RNA degradation [Source:HGNC Symbol;Acc:HGNC:21056]","synonyms":"FLJ11152,dJ266L20.3,C6orf70","biotype":"protein_coding","ncbi_id":"55780","summary":"The protein encoded by this gene contains 2 transmembrane domains near the C-terminus and is localized in the endoplasmic reticulum. Knockout of this gene in developing rat brain showed that it may be involved in neuronal migration. Mutations in this gene are associated with periventricular nodular heterotopia-6 (PVNH6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":169751622,"end":169781584,"strand":1,"description":"ER membrane associated RNA degradation [Source:HGNC Symbol;Acc:HGNC:21056]"}, {"versioned_ensembl_gene_id":"ENSG00000268565.1","gene_symbol":"AC005339.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4654964,"end":4655524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140104.13","gene_symbol":"C14orf79","gene_name":"chromosome 14 open reading frame 79 [Source:HGNC Symbol;Acc:HGNC:20126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122616","summary":null,"start":104985775,"end":105010482,"strand":1,"description":"chromosome 14 open reading frame 79 [Source:HGNC Symbol;Acc:HGNC:20126]"}, {"versioned_ensembl_gene_id":"ENSG00000277823.3","gene_symbol":"PRH1","gene_name":"proline rich protein HaeIII subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9366]","synonyms":"Pa","biotype":"protein_coding","ncbi_id":"5554","summary":"This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. Multiple distinct alleles of this locus including the parotid isoelectric-focusing variant slow (PIF-s), the parotid acidic protein (Pa), and the double band slow (Db-s) isoforms have been characterized. The reference genome encodes the Db-s allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Co-transcription of this gene with adjacent genes has been observed. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]","start":10824960,"end":11167778,"strand":-1,"description":"proline rich protein HaeIII subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9366]"}, {"versioned_ensembl_gene_id":"ENSG00000266896.1","gene_symbol":"AL354892.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":169770413,"end":169772042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277254.1","gene_symbol":"TAS2R13","gene_name":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]","synonyms":"TRB3,T2R13","biotype":"protein_coding","ncbi_id":"50838","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10907926,"end":10909562,"strand":-1,"description":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]"}, {"versioned_ensembl_gene_id":"ENSG00000239445.5","gene_symbol":"ST3GAL6-AS1","gene_name":"ST3GAL6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40828]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874207","summary":null,"start":98714330,"end":98732651,"strand":-1,"description":"ST3GAL6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40828]"}, {"versioned_ensembl_gene_id":"ENSG00000278307.3","gene_symbol":"TAS2R19","gene_name":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]","synonyms":"TAS2R48,TAS2R23,T2R23,T2R19","biotype":"protein_coding","ncbi_id":"259294","summary":null,"start":11021607,"end":11022608,"strand":-1,"description":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]"}, {"versioned_ensembl_gene_id":"ENSG00000205853.10","gene_symbol":"RFPL3S","gene_name":"RFPL3 antisense [Source:HGNC Symbol;Acc:HGNC:9981]","synonyms":"RFPL3-AS1,RFPL3-AS,NCRNA00005","biotype":"protein_coding","ncbi_id":"10737","summary":null,"start":32359906,"end":32382052,"strand":-1,"description":"RFPL3 antisense [Source:HGNC Symbol;Acc:HGNC:9981]"}, {"versioned_ensembl_gene_id":"ENSG00000008441.16","gene_symbol":"NFIX","gene_name":"nuclear factor I X [Source:HGNC Symbol;Acc:HGNC:7788]","synonyms":"NF1A","biotype":"protein_coding","ncbi_id":"4784","summary":"The protein encoded by this gene is a transcription factor that binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3 in viral and cellular promoters. The encoded protein can also stimulate adenovirus replication in vitro. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2012]","start":12995608,"end":13098796,"strand":1,"description":"nuclear factor I X [Source:HGNC Symbol;Acc:HGNC:7788]"}, {"versioned_ensembl_gene_id":"ENSG00000170779.10","gene_symbol":"CDCA4","gene_name":"cell division cycle associated 4 [Source:HGNC Symbol;Acc:HGNC:14625]","synonyms":"Hepp,FLJ20764","biotype":"protein_coding","ncbi_id":"55038","summary":"This gene encodes a protein that belongs to the E2F family of transcription factors. This protein regulates E2F-dependent transcriptional activation and cell proliferation, mainly through the E2F/retinoblastoma protein pathway. It also functions in the regulation of JUN oncogene expression. This protein shows distinctive nuclear-mitotic apparatus distribution, it is involved in spindle organization from prometaphase, and may also play a role as a midzone factor involved in chromosome segregation or cytokinesis. Two alternatively spliced transcript variants encoding the same protein have been noted for this gene. Two pseudogenes have also been identified on chromosome 1. [provided by RefSeq, May 2014]","start":105009573,"end":105021148,"strand":-1,"description":"cell division cycle associated 4 [Source:HGNC Symbol;Acc:HGNC:14625]"}, {"versioned_ensembl_gene_id":"ENSG00000241954.1","gene_symbol":"AL021937.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32383786,"end":32385631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228382.1","gene_symbol":"ITPKB-IT1","gene_name":"ITPKB intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41349]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506443","summary":null,"start":226656640,"end":226675067,"strand":-1,"description":"ITPKB intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41349]"}, {"versioned_ensembl_gene_id":"ENSG00000136153.19","gene_symbol":"LMO7","gene_name":"LIM domain 7 [Source:HGNC Symbol;Acc:HGNC:6646]","synonyms":"KIAA0858,FBXO20,FBX20","biotype":"protein_coding","ncbi_id":"4008","summary":"This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009]","start":75620434,"end":75859870,"strand":1,"description":"LIM domain 7 [Source:HGNC Symbol;Acc:HGNC:6646]"}, {"versioned_ensembl_gene_id":"ENSG00000128276.10","gene_symbol":"RFPL3","gene_name":"ret finger protein like 3 [Source:HGNC Symbol;Acc:HGNC:9980]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10738","summary":null,"start":32354885,"end":32361161,"strand":1,"description":"ret finger protein like 3 [Source:HGNC Symbol;Acc:HGNC:9980]"}, {"versioned_ensembl_gene_id":"ENSG00000261553.5","gene_symbol":"AL137782.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75549773,"end":75807120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254166.2","gene_symbol":"CASC19","gene_name":"cancer susceptibility 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49476]","synonyms":"CARLo-6,LINC01245","biotype":"processed_transcript","ncbi_id":"103021165","summary":null,"start":127072694,"end":127227541,"strand":-1,"description":"cancer susceptibility 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49476]"}, {"versioned_ensembl_gene_id":"ENSG00000243519.1","gene_symbol":"IGLVIVOR22-2","gene_name":"immunoglobulin lambda variable (IV)/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15695]","synonyms":"IGLV(IV)/OR22-2","biotype":"IG_V_pseudogene","ncbi_id":"84087","summary":null,"start":32376682,"end":32377135,"strand":1,"description":"immunoglobulin lambda variable (IV)/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15695]"}, {"versioned_ensembl_gene_id":"ENSG00000261105.5","gene_symbol":"LMO7-AS1","gene_name":"LMO7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50277]","synonyms":"UCHL3-AS1","biotype":"antisense_RNA","ncbi_id":"101927155","summary":null,"start":75604700,"end":75635994,"strand":-1,"description":"LMO7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50277]"}, {"versioned_ensembl_gene_id":"ENSG00000224722.3","gene_symbol":"AC020688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127086263,"end":127087510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217128.11","gene_symbol":"FNIP1","gene_name":"folliculin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29418]","synonyms":"KIAA1961","biotype":"protein_coding","ncbi_id":"96459","summary":"This gene encodes a protein that binds to the tumor suppressor protein folliculin and to AMP-activated protein kinase (AMPK). The encoded protein participates in the regulation of cellular metabolism and nutrient sensing by modulating the AMPK and target of rapamycin signaling pathways. This gene has a closely related paralog that encodes a protein with similar binding activities. Both related proteins also associate with the molecular chaperone heat shock protein-90 (Hsp90) and negatively regulate its ATPase activity and facilitate its association with folliculin. [provided by RefSeq, Jul 2017]","start":131641714,"end":131797063,"strand":-1,"description":"folliculin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29418]"}, {"versioned_ensembl_gene_id":"ENSG00000282961.1","gene_symbol":"PRNCR1","gene_name":"prostate cancer associated non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:48942]","synonyms":"PCAT8","biotype":"lincRNA","ncbi_id":"101867536","summary":null,"start":127079874,"end":127092600,"strand":1,"description":"prostate cancer associated non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:48942]"}, {"versioned_ensembl_gene_id":"ENSG00000238837.3","gene_symbol":"LINC02031","gene_name":"long intergenic non-protein coding RNA 2031 [Source:HGNC Symbol;Acc:HGNC:52865]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724617","summary":null,"start":182644214,"end":182655880,"strand":1,"description":"long intergenic non-protein coding RNA 2031 [Source:HGNC Symbol;Acc:HGNC:52865]"}, {"versioned_ensembl_gene_id":"ENSG00000203852.3","gene_symbol":"HIST2H3A","gene_name":"histone cluster 2 H3 family member a [Source:HGNC Symbol;Acc:HGNC:20505]","synonyms":"H3/o,H3/n","biotype":"protein_coding","ncbi_id":"333932","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the centromeric copy. [provided by RefSeq, Aug 2015]","start":149852619,"end":149854274,"strand":1,"description":"histone cluster 2 H3 family member a [Source:HGNC Symbol;Acc:HGNC:20505]"}, {"versioned_ensembl_gene_id":"ENSG00000101096.19","gene_symbol":"NFATC2","gene_name":"nuclear factor of activated T-cells 2 [Source:HGNC Symbol;Acc:HGNC:7776]","synonyms":"NFATp,NFAT1,NF-ATP","biotype":"protein_coding","ncbi_id":"4773","summary":"This gene is a member of the nuclear factor of activated T cells (NFAT) family. The product of this gene is a DNA-binding protein with a REL-homology region (RHR) and an NFAT-homology region (NHR). This protein is present in the cytosol and only translocates to the nucleus upon T cell receptor (TCR) stimulation, where it becomes a member of the nuclear factors of activated T cells transcription complex. This complex plays a central role in inducing gene transcription during the immune response. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Apr 2012]","start":51386957,"end":51562831,"strand":-1,"description":"nuclear factor of activated T-cells 2 [Source:HGNC Symbol;Acc:HGNC:7776]"}, {"versioned_ensembl_gene_id":"ENSG00000245105.2","gene_symbol":"A2M-AS1","gene_name":"A2M antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27057]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"144571","summary":null,"start":9065177,"end":9068060,"strand":1,"description":"A2M antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27057]"}, {"versioned_ensembl_gene_id":"ENSG00000177684.3","gene_symbol":"DEFB114","gene_name":"defensin beta 114 [Source:HGNC Symbol;Acc:HGNC:18095]","synonyms":"DEFB-14","biotype":"protein_coding","ncbi_id":"245928","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. The protein encoded by this gene is a beta-defensin with antimicrobial activity against E. coli, S. aureus, and C. albicans. The encoded protein also binds and neutralizes lipopolysaccharide (LPS), a factor involved in inflammatory diseases and male reproductive issues. [provided by RefSeq, Nov 2014]","start":49960249,"end":49964105,"strand":-1,"description":"defensin beta 114 [Source:HGNC Symbol;Acc:HGNC:18095]"}, {"versioned_ensembl_gene_id":"ENSG00000270494.1","gene_symbol":"AL513534.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68717311,"end":68717795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225815.2","gene_symbol":"AC092669.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66327349,"end":66328984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213500.3","gene_symbol":"LAP3P2","gene_name":"leucine aminopeptidase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42365]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389386","summary":null,"start":36673817,"end":36675270,"strand":1,"description":"leucine aminopeptidase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42365]"}, {"versioned_ensembl_gene_id":"ENSG00000279044.1","gene_symbol":"AC007787.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":13081966,"end":13082564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277791.4","gene_symbol":"PSMB3","gene_name":"proteasome subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:9540]","synonyms":"MGC4147,HC10-II","biotype":"protein_coding","ncbi_id":"5691","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. The 26 S proteasome may be involved in trinucleotide repeat expansion, a phenomenon which is associated with many hereditary neurological diseases. Pseudogenes have been identified on chromosomes 2 and 12. Alternative splicing results in multiple transcript variants [provided by RefSeq, Sep 2013]","start":38752736,"end":38764231,"strand":1,"description":"proteasome subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:9540]"}, {"versioned_ensembl_gene_id":"ENSG00000139826.5","gene_symbol":"ABHD13","gene_name":"abhydrolase domain containing 13 [Source:HGNC Symbol;Acc:HGNC:20293]","synonyms":"FLJ14906,C13orf6,BEM46L1,bA153I24.2","biotype":"protein_coding","ncbi_id":"84945","summary":null,"start":108218379,"end":108234255,"strand":1,"description":"abhydrolase domain containing 13 [Source:HGNC Symbol;Acc:HGNC:20293]"}, {"versioned_ensembl_gene_id":"ENSG00000066455.12","gene_symbol":"GOLGA5","gene_name":"golgin A5 [Source:HGNC Symbol;Acc:HGNC:4428]","synonyms":"rfg5,ret-II,GOLIM5,golgin-84","biotype":"protein_coding","ncbi_id":"9950","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This protein is a coiled-coil membrane protein that has been postulated to play a role in vesicle tethering and docking. Translocations involving this gene and the ret proto-oncogene have been found in tumor tissues; the chimeric sequences have been designated RET-II and PTC5. A pseudogene of this gene is located on the short arm of chromosome 5. [provided by RefSeq, Jul 2013]","start":92794231,"end":92839963,"strand":1,"description":"golgin A5 [Source:HGNC Symbol;Acc:HGNC:4428]"}, {"versioned_ensembl_gene_id":"ENSG00000254535.3","gene_symbol":"PABPC4L","gene_name":"poly(A) binding protein cytoplasmic 4 like [Source:HGNC Symbol;Acc:HGNC:31955]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132430","summary":null,"start":134196333,"end":134201748,"strand":-1,"description":"poly(A) binding protein cytoplasmic 4 like [Source:HGNC Symbol;Acc:HGNC:31955]"}, {"versioned_ensembl_gene_id":"ENSG00000197562.9","gene_symbol":"RAB40C","gene_name":"RAB40C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18285]","synonyms":"RASL8C,RARL","biotype":"protein_coding","ncbi_id":"57799","summary":null,"start":589357,"end":629272,"strand":1,"description":"RAB40C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18285]"}, {"versioned_ensembl_gene_id":"ENSG00000271776.1","gene_symbol":"AL445209.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78596129,"end":78599619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143772.9","gene_symbol":"ITPKB","gene_name":"inositol-trisphosphate 3-kinase B [Source:HGNC Symbol;Acc:HGNC:6179]","synonyms":"IP3KB,IP3-3KB","biotype":"protein_coding","ncbi_id":"3707","summary":"The protein encoded by this protein regulates inositol phosphate metabolism by phosphorylation of second messenger inositol 1,4,5-trisphosphate to Ins(1,3,4,5)P4. The activity of this encoded protein is responsible for regulating the levels of a large number of inositol polyphosphates that are important in cellular signaling. Both calcium/calmodulin and protein phosphorylation mechanisms control its activity. [provided by RefSeq, Jul 2008]","start":226631690,"end":226739323,"strand":-1,"description":"inositol-trisphosphate 3-kinase B [Source:HGNC Symbol;Acc:HGNC:6179]"}, {"versioned_ensembl_gene_id":"ENSG00000228548.1","gene_symbol":"ITPKB-AS1","gene_name":"ITPKB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40312]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873994","summary":null,"start":226668897,"end":226676345,"strand":1,"description":"ITPKB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40312]"}, {"versioned_ensembl_gene_id":"ENSG00000230624.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"D6S81E,BAT1,UAP56","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31512399,"end":31528755,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000272994.1","gene_symbol":"AC012360.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105334027,"end":105337475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231975.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31510897,"end":31512412,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000244153.1","gene_symbol":"WWP1P1","gene_name":"WW domain containing E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48944]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339843","summary":null,"start":98657802,"end":98660570,"strand":1,"description":"WW domain containing E3 ubiquitin protein ligase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48944]"}, {"versioned_ensembl_gene_id":"ENSG00000260400.1","gene_symbol":"AL513534.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":68698500,"end":68700794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182359.14","gene_symbol":"KBTBD3","gene_name":"kelch repeat and BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22934]","synonyms":"BKLHD3","biotype":"protein_coding","ncbi_id":"143879","summary":null,"start":106051098,"end":106077765,"strand":-1,"description":"kelch repeat and BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22934]"}, {"versioned_ensembl_gene_id":"ENSG00000234512.1","gene_symbol":"TLR12P","gene_name":"toll like receptor 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:31754]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100131451","summary":null,"start":33466249,"end":33468954,"strand":1,"description":"toll like receptor 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:31754]"}, {"versioned_ensembl_gene_id":"ENSG00000244199.1","gene_symbol":"EIF4EP3","gene_name":"eukaryotic translation initiation factor 4E pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51461]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132918","summary":null,"start":182460417,"end":182461072,"strand":-1,"description":"eukaryotic translation initiation factor 4E pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51461]"}, {"versioned_ensembl_gene_id":"ENSG00000242012.1","gene_symbol":"AC084211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182365147,"end":182368256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179766.18","gene_symbol":"ATP8B5P","gene_name":"ATPase phospholipid transporting 8B5, pseudogene [Source:HGNC Symbol;Acc:HGNC:27245]","synonyms":"FetA","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"158381","summary":null,"start":35406755,"end":35483035,"strand":1,"description":"ATPase phospholipid transporting 8B5, pseudogene [Source:HGNC Symbol;Acc:HGNC:27245]"}, {"versioned_ensembl_gene_id":"ENSG00000205978.5","gene_symbol":"NYNRIN","gene_name":"NYN domain and retroviral integrase containing [Source:HGNC Symbol;Acc:HGNC:20165]","synonyms":"KIAA1305,FLJ11811,CGIN1","biotype":"protein_coding","ncbi_id":"57523","summary":null,"start":24398786,"end":24419288,"strand":1,"description":"NYN domain and retroviral integrase containing [Source:HGNC Symbol;Acc:HGNC:20165]"}, {"versioned_ensembl_gene_id":"ENSG00000250959.2","gene_symbol":"GLUD1P3","gene_name":"glutamate dehydrogenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4338]","synonyms":"GLUDP3,Em:AC022400.11,C10orf102","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"2749","summary":null,"start":73730562,"end":73737311,"strand":1,"description":"glutamate dehydrogenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4338]"}, {"versioned_ensembl_gene_id":"ENSG00000251087.3","gene_symbol":"ALG1L3P","gene_name":"asparagine-linked glycosylation 1-like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44372]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132066","summary":null,"start":9703754,"end":9710812,"strand":-1,"description":"asparagine-linked glycosylation 1-like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44372]"}, {"versioned_ensembl_gene_id":"ENSG00000254698.1","gene_symbol":"AP000893.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":82963681,"end":83039115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274327.1","gene_symbol":"TAS2R7","gene_name":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]","synonyms":"TRB4,T2R7","biotype":"protein_coding","ncbi_id":"50837","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10801532,"end":10802627,"strand":-1,"description":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]"}, {"versioned_ensembl_gene_id":"ENSG00000155827.11","gene_symbol":"RNF20","gene_name":"ring finger protein 20 [Source:HGNC Symbol;Acc:HGNC:10062]","synonyms":"KAIA2779,hBRE1,FLJ20382,FLJ11189,BRE1A,BRE1","biotype":"protein_coding","ncbi_id":"56254","summary":"The protein encoded by this gene shares similarity with BRE1 of S. cerevisiae. The protein encoded by this human gene is an E3 ubiquitin ligase that regulates chromosome structure by monoubiquitinating histone H2B. This protein acts as a putative tumor suppressor and positively regulates the p53 tumor suppressor as well as numerous histone H2A and H2B genes. In contrast, this protein also suppresses the expression of several protooncogenes and growth-related genes, including many genes that are induced by epidermal growth factor. This gene selectively suppresses the expression of some genes by interfering with chromatin recruitment of transcription elongation factor SII (TFIIS). [provided by RefSeq, Feb 2012]","start":101533851,"end":101563344,"strand":1,"description":"ring finger protein 20 [Source:HGNC Symbol;Acc:HGNC:10062]"}, {"versioned_ensembl_gene_id":"ENSG00000268119.5","gene_symbol":"AC010615.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":21444241,"end":21463908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229535.1","gene_symbol":"CR753820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31510294,"end":31510873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123171.6","gene_symbol":"CCDC70","gene_name":"coiled-coil domain containing 70 [Source:HGNC Symbol;Acc:HGNC:25303]","synonyms":"FLJ25853,DKFZP434K1172","biotype":"protein_coding","ncbi_id":"83446","summary":null,"start":51861981,"end":51866232,"strand":1,"description":"coiled-coil domain containing 70 [Source:HGNC Symbol;Acc:HGNC:25303]"}, {"versioned_ensembl_gene_id":"ENSG00000256403.1","gene_symbol":"AP003785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72410716,"end":72412079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132953.16","gene_symbol":"XPO4","gene_name":"exportin 4 [Source:HGNC Symbol;Acc:HGNC:17796]","synonyms":"KIAA1721,FLJ13046","biotype":"protein_coding","ncbi_id":"64328","summary":"XPO4 belongs to a large family of karyopherins (see MIM 602738) that mediate the transport of proteins and other cargo between the nuclear and cytoplasmic compartments (Lipowsky et al., 2000 [PubMed 10944119]).[supplied by OMIM, Mar 2009]","start":20777329,"end":20903048,"strand":-1,"description":"exportin 4 [Source:HGNC Symbol;Acc:HGNC:17796]"}, {"versioned_ensembl_gene_id":"ENSG00000272196.2","gene_symbol":"HIST2H2AA4","gene_name":"histone cluster 2 H2A family member a4 [Source:HGNC Symbol;Acc:HGNC:29668]","synonyms":"H2A/r","biotype":"protein_coding","ncbi_id":"723790","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the telomeric copy. [provided by RefSeq, Aug 2015]","start":149851061,"end":149851624,"strand":1,"description":"histone cluster 2 H2A family member a4 [Source:HGNC Symbol;Acc:HGNC:29668]"}, {"versioned_ensembl_gene_id":"ENSG00000231118.3","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31501676,"end":31502487,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000108349.16","gene_symbol":"CASC3","gene_name":"cancer susceptibility 3 [Source:HGNC Symbol;Acc:HGNC:17040]","synonyms":"MLN51,BTZ","biotype":"protein_coding","ncbi_id":"22794","summary":"The product of this gene is a core component of the exon junction complex (EJC), a protein complex that is deposited on spliced mRNAs at exon-exon junctions and functions in nonsense-mediated mRNA decay (NMD). The encoded protein binds RNA and interacts with two other EJC core components. It is predominantly located in the cytoplasm, but shuttles into the nucleus where it localizes to nuclear speckles. [provided by RefSeq, Jul 2008]","start":40140318,"end":40172183,"strand":1,"description":"cancer susceptibility 3 [Source:HGNC Symbol;Acc:HGNC:17040]"}, {"versioned_ensembl_gene_id":"ENSG00000006377.10","gene_symbol":"DLX6","gene_name":"distal-less homeobox 6 [Source:HGNC Symbol;Acc:HGNC:2919]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1750","summary":"This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This family is comprised of at least 6 different members that encode proteins with roles in forebrain and craniofacial development. This gene is in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7. [provided by RefSeq, Jul 2008]","start":97005548,"end":97011039,"strand":1,"description":"distal-less homeobox 6 [Source:HGNC Symbol;Acc:HGNC:2919]"}, {"versioned_ensembl_gene_id":"ENSG00000229965.1","gene_symbol":"AL359704.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226438564,"end":226439344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272993.1","gene_symbol":"AC239868.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149845816,"end":149846486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220323.3","gene_symbol":"AC239868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149843041,"end":149843533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203812.2","gene_symbol":"HIST2H2AA3","gene_name":"histone cluster 2 H2A family member a3 [Source:HGNC Symbol;Acc:HGNC:4736]","synonyms":"H2AFO,H2A/q,H2A.2,HIST2H2AA","biotype":"protein_coding","ncbi_id":"8337","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the centromeric copy. [provided by RefSeq, Aug 2015]","start":149842188,"end":149842736,"strand":-1,"description":"histone cluster 2 H2A family member a3 [Source:HGNC Symbol;Acc:HGNC:4736]"}, {"versioned_ensembl_gene_id":"ENSG00000267552.6","gene_symbol":"AC093227.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37689865,"end":37719188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136603.13","gene_symbol":"SKIL","gene_name":"SKI like proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10897]","synonyms":"SnoN,SnoA,SNO","biotype":"protein_coding","ncbi_id":"6498","summary":"The protein encoded by this gene is a component of the SMAD pathway, which regulates cell growth and differentiation through transforming growth factor-beta (TGFB). In the absence of ligand, the encoded protein binds to the promoter region of TGFB-responsive genes and recruits a nuclear repressor complex. TGFB signaling causes SMAD3 to enter the nucleus and degrade this protein, allowing these genes to be activated. Four transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":170357678,"end":170396835,"strand":1,"description":"SKI like proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10897]"}, {"versioned_ensembl_gene_id":"ENSG00000259420.5","gene_symbol":"AC046168.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77568970,"end":77608888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225254.2","gene_symbol":"ARMC8P1","gene_name":"armadillo repeat containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49918]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130871","summary":null,"start":38452782,"end":38454070,"strand":-1,"description":"armadillo repeat containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49918]"}, {"versioned_ensembl_gene_id":"ENSG00000249690.1","gene_symbol":"AC110813.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150579089,"end":150581545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204442.3","gene_symbol":"FAM155A","gene_name":"family with sequence similarity 155 member A [Source:HGNC Symbol;Acc:HGNC:33877]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728215","summary":null,"start":107163510,"end":107866735,"strand":-1,"description":"family with sequence similarity 155 member A [Source:HGNC Symbol;Acc:HGNC:33877]"}, {"versioned_ensembl_gene_id":"ENSG00000248521.1","gene_symbol":"AC092612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150422645,"end":150423642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136840.18","gene_symbol":"ST6GALNAC4","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:17846]","synonyms":"SIAT3C,ST6GALNACIV,SIAT7D","biotype":"protein_coding","ncbi_id":"27090","summary":"The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein prefers glycoproteins rather than glycolipids as substrates and shows restricted substrate specificity, utilizing only the trisaccharide sequence Neu5Ac-alpha-2,3-Gal-beta-1,3-GalNAc. In addition, it is involved in the synthesis of ganglioside GD1A from GM1B. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":127907886,"end":127917038,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:17846]"}, {"versioned_ensembl_gene_id":"ENSG00000175899.14","gene_symbol":"A2M","gene_name":"alpha-2-macroglobulin [Source:HGNC Symbol;Acc:HGNC:7]","synonyms":"S863-7,FWP007,CPAMD5","biotype":"protein_coding","ncbi_id":"2","summary":"The protein encoded by this gene is a protease inhibitor and cytokine transporter. It uses a bait-and-trap mechanism to inhibit a broad spectrum of proteases, including trypsin, thrombin and collagenase. It can also inhibit inflammatory cytokines, and it thus disrupts inflammatory cascades. Mutations in this gene are a cause of alpha-2-macroglobulin deficiency. This gene is implicated in Alzheimer's disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. A related pseudogene, which is also located on the p arm of chromosome 12, has been identified. [provided by RefSeq, Nov 2016]","start":9067664,"end":9116229,"strand":-1,"description":"alpha-2-macroglobulin [Source:HGNC Symbol;Acc:HGNC:7]"}, {"versioned_ensembl_gene_id":"ENSG00000242291.1","gene_symbol":"RPL36AP51","gene_name":"ribosomal protein L36a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36632]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649299","summary":null,"start":21233335,"end":21233652,"strand":1,"description":"ribosomal protein L36a pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36632]"}, {"versioned_ensembl_gene_id":"ENSG00000276053.4","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54359738,"end":54378912,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000250670.1","gene_symbol":"AC004063.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104556960,"end":104568877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245384.1","gene_symbol":"CXXC4-AS1","gene_name":"CXXC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41054]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929468","summary":null,"start":104490965,"end":104697592,"strand":1,"description":"CXXC4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41054]"}, {"versioned_ensembl_gene_id":"ENSG00000214881.4","gene_symbol":"TMEM14DP","gene_name":"transmembrane protein 14D, pseudogene [Source:HGNC Symbol;Acc:HGNC:15660]","synonyms":"TMEM14D,bA524O24.3","biotype":"processed_pseudogene","ncbi_id":"645203","summary":null,"start":68544489,"end":68544833,"strand":-1,"description":"transmembrane protein 14D, pseudogene [Source:HGNC Symbol;Acc:HGNC:15660]"}, {"versioned_ensembl_gene_id":"ENSG00000268326.1","gene_symbol":"AC008739.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20972262,"end":20983210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268081.1","gene_symbol":"AC123912.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21554640,"end":21569237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183978.7","gene_symbol":"COA3","gene_name":"cytochrome c oxidase assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:24990]","synonyms":"MITRAC12,HSPC009,COX25,CCDC56","biotype":"protein_coding","ncbi_id":"28958","summary":"This gene encodes a member of the cytochrome c oxidase assembly factor family. Studies of a related gene in fly suggest that the encoded protein is localized to mitochondria and is essential for cytochrome c oxidase function. [provided by RefSeq, Nov 2012]","start":42795147,"end":42798704,"strand":-1,"description":"cytochrome c oxidase assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:24990]"}, {"versioned_ensembl_gene_id":"ENSG00000104442.9","gene_symbol":"ARMC1","gene_name":"armadillo repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:17684]","synonyms":"FLJ10511,Arcp","biotype":"protein_coding","ncbi_id":"55156","summary":null,"start":65602456,"end":65634217,"strand":-1,"description":"armadillo repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:17684]"}, {"versioned_ensembl_gene_id":"ENSG00000088836.12","gene_symbol":"SLC4A11","gene_name":"solute carrier family 4 member 11 [Source:HGNC Symbol;Acc:HGNC:16438]","synonyms":"NaBC1,FECD4,dJ794I6.2,CHED2,CDPD1,BTR1","biotype":"protein_coding","ncbi_id":"83959","summary":"This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]","start":3227417,"end":3239190,"strand":-1,"description":"solute carrier family 4 member 11 [Source:HGNC Symbol;Acc:HGNC:16438]"}, {"versioned_ensembl_gene_id":"ENSG00000215165.3","gene_symbol":"TCEA1P3","gene_name":"transcription elongation factor A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30569]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340501","summary":null,"start":38478471,"end":38479350,"strand":1,"description":"transcription elongation factor A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30569]"}, {"versioned_ensembl_gene_id":"ENSG00000071537.13","gene_symbol":"SEL1L","gene_name":"SEL1L ERAD E3 ligase adaptor subunit [Source:HGNC Symbol;Acc:HGNC:10717]","synonyms":"SEL1L1,IBD2","biotype":"protein_coding","ncbi_id":"6400","summary":"The protein encoded by this gene is part of a protein complex required for the retrotranslocation or dislocation of misfolded proteins from the endoplasmic reticulum lumen to the cytosol, where they are degraded by the proteasome in a ubiquitin-dependent manner. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":81471549,"end":81533861,"strand":-1,"description":"SEL1L ERAD E3 ligase adaptor subunit [Source:HGNC Symbol;Acc:HGNC:10717]"}, {"versioned_ensembl_gene_id":"ENSG00000229511.1","gene_symbol":"GAS2L1P1","gene_name":"growth arrest specific 2 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50293]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927222","summary":null,"start":38486859,"end":38488338,"strand":-1,"description":"growth arrest specific 2 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50293]"}, {"versioned_ensembl_gene_id":"ENSG00000243085.1","gene_symbol":"AL390726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38526831,"end":38527032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283706.1","gene_symbol":"PRSS50","gene_name":"protease, serine 50 [Source:HGNC Symbol;Acc:HGNC:17910]","synonyms":"TSP50,CT20,TSP50,CT20","biotype":"protein_coding","ncbi_id":"29122","summary":null,"start":46712115,"end":46717907,"strand":-1,"description":"protease, serine 50 [Source:HGNC Symbol;Acc:HGNC:17910]"}, {"versioned_ensembl_gene_id":"ENSG00000164002.11","gene_symbol":"EXO5","gene_name":"exonuclease 5 [Source:HGNC Symbol;Acc:HGNC:26115]","synonyms":"FLJ21144,DEM1,C1orf176","biotype":"protein_coding","ncbi_id":"64789","summary":"The protein encoded by this gene is a single-stranded DNA (ssDNA)-specific exonuclease that can slide along the DNA before cutting it. However, human replication protein A binds ssDNA and restricts sliding of the encoded protein, providing a 5'-directionality to the enzyme. This protein localizes to nuclear repair loci after DNA damage. [provided by RefSeq, Nov 2016]","start":40508741,"end":40516556,"strand":1,"description":"exonuclease 5 [Source:HGNC Symbol;Acc:HGNC:26115]"}, {"versioned_ensembl_gene_id":"ENSG00000124812.14","gene_symbol":"CRISP1","gene_name":"cysteine rich secretory protein 1 [Source:HGNC Symbol;Acc:HGNC:304]","synonyms":"AEGL1,HUMARP,HSCRISP1G,HSCRISP1D,CRISP-1,ARP","biotype":"protein_coding","ncbi_id":"167","summary":"Fertilization consists of a sequence of specific cell-cell interactions culminating in the fusion of the sperm and egg plasma membranes. Recognition, binding, and fusion occur through the interaction of complementary molecules that are localized to specific domains of the sperm and egg plasma membranes. In the sperm, the postacrosomal region or equatorial segment is involved in sperm-egg plasma membrane fusion. The protein encoded by this gene is a member of the cysteine-rich secretory protein (CRISP) family. It is expressed in the epididymis, is secreted into the epididymal lumen, and binds to the postacrosomal region of the sperm head, where it plays a role in sperm-egg fusion. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":49834257,"end":49877096,"strand":-1,"description":"cysteine rich secretory protein 1 [Source:HGNC Symbol;Acc:HGNC:304]"}, {"versioned_ensembl_gene_id":"ENSG00000244004.1","gene_symbol":"AC097493.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9563171,"end":9563950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126562.16","gene_symbol":"WNK4","gene_name":"WNK lysine deficient protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:14544]","synonyms":"PRKWNK4","biotype":"protein_coding","ncbi_id":"65266","summary":"This gene encodes a member of the WNK family of serine-threonine protein kinases. The kinase is part of the tight junction complex in kidney cells, and regulates the balance between NaCl reabsorption and K(+) secretion. The kinase regulates the activities of several types of ion channels, cotransporters, and exchangers involved in electrolyte flux in epithelial cells. Mutations in this gene result in pseudohypoaldosteronism type IIB.[provided by RefSeq, Sep 2009]","start":42780678,"end":42796936,"strand":1,"description":"WNK lysine deficient protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:14544]"}, {"versioned_ensembl_gene_id":"ENSG00000253489.1","gene_symbol":"AC009930.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111179193,"end":111179872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196705.8","gene_symbol":"ZNF431","gene_name":"zinc finger protein 431 [Source:HGNC Symbol;Acc:HGNC:20809]","synonyms":"KIAA1969","biotype":"protein_coding","ncbi_id":"170959","summary":"This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein may negatively regulate transcription of target genes, including the hedgehog signaling pathway receptor patched 1, by interacting with histone deacetylases. Mutations in this gene may be associated with non-syndromic facial clefting in human patients. [provided by RefSeq, Jul 2016]","start":21142024,"end":21196053,"strand":1,"description":"zinc finger protein 431 [Source:HGNC Symbol;Acc:HGNC:20809]"}, {"versioned_ensembl_gene_id":"ENSG00000272934.1","gene_symbol":"AL390726.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":38542389,"end":38543215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214071.4","gene_symbol":"BX842568.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37077851,"end":37078401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224018.1","gene_symbol":"AP000470.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24155170,"end":24188342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269237.1","gene_symbol":"AC010615.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21405159,"end":21491266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269839.1","gene_symbol":"AC010620.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21225098,"end":21245241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243048.3","gene_symbol":"FTH1P18","gene_name":"ferritin heavy chain 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:3988]","synonyms":"FTHL18","biotype":"unprocessed_pseudogene","ncbi_id":"441490","summary":null,"start":37043023,"end":37043571,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:3988]"}, {"versioned_ensembl_gene_id":"ENSG00000279404.1","gene_symbol":"AC008739.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20926777,"end":20928714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268747.1","gene_symbol":"AC022432.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21276023,"end":21276332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235564.1","gene_symbol":"AP000477.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23960905,"end":23967273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259115.1","gene_symbol":"AL357153.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70593314,"end":70641204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258951.1","gene_symbol":"KRT18P7","gene_name":"keratin 18 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:20283]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418877","summary":null,"start":70594552,"end":70595770,"strand":1,"description":"keratin 18 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:20283]"}, {"versioned_ensembl_gene_id":"ENSG00000181585.3","gene_symbol":"TMIE","gene_name":"transmembrane inner ear [Source:HGNC Symbol;Acc:HGNC:30800]","synonyms":"DFNB6","biotype":"protein_coding","ncbi_id":"259236","summary":"This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment. [provided by RefSeq, Mar 2009]","start":46701333,"end":46710886,"strand":1,"description":"transmembrane inner ear [Source:HGNC Symbol;Acc:HGNC:30800]"}, {"versioned_ensembl_gene_id":"ENSG00000163235.15","gene_symbol":"TGFA","gene_name":"transforming growth factor alpha [Source:HGNC Symbol;Acc:HGNC:11765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7039","summary":"This gene encodes a growth factor that is a ligand for the epidermal growth factor receptor, which activates a signaling pathway for cell proliferation, differentiation and development. This protein may act as either a transmembrane-bound ligand or a soluble ligand. This gene has been associated with many types of cancers, and it may also be involved in some cases of cleft lip/palate. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":70447280,"end":70554193,"strand":-1,"description":"transforming growth factor alpha [Source:HGNC Symbol;Acc:HGNC:11765]"}, {"versioned_ensembl_gene_id":"ENSG00000071859.14","gene_symbol":"FAM50A","gene_name":"family with sequence similarity 50 member A [Source:HGNC Symbol;Acc:HGNC:18786]","synonyms":"XAP5,HXC-26,DXS9928E,9F","biotype":"protein_coding","ncbi_id":"9130","summary":"This gene belongs to the FAM50 family. The encoded protein is highly conserved in length and sequence across different species. It is a basic protein containing a nuclear localization signal, and may function as a DNA-binding protein or a transcriptional factor. [provided by RefSeq, Sep 2009]","start":154444126,"end":154450654,"strand":1,"description":"family with sequence similarity 50 member A [Source:HGNC Symbol;Acc:HGNC:18786]"}, {"versioned_ensembl_gene_id":"ENSG00000245311.2","gene_symbol":"ARNTL2-AS1","gene_name":"ARNTL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49892]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928646","summary":null,"start":27389789,"end":27446625,"strand":-1,"description":"ARNTL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49892]"}, {"versioned_ensembl_gene_id":"ENSG00000255776.1","gene_symbol":"VDAC2P2","gene_name":"voltage dependent anion channel 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643996","summary":null,"start":9036344,"end":9037244,"strand":1,"description":"voltage dependent anion channel 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32693]"}, {"versioned_ensembl_gene_id":"ENSG00000224050.1","gene_symbol":"AL008723.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32273420,"end":32277186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169403.11","gene_symbol":"PTAFR","gene_name":"platelet activating factor receptor [Source:HGNC Symbol;Acc:HGNC:9582]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5724","summary":"This gene encodes a seven-transmembrane G-protein-coupled receptor for platelet-activating factor (PAF) that localizes to lipid rafts and/or caveolae in the cell membrane. PAF (1-0-alkyl-2-acetyl-sn-glycero-3-phosphorylcholine) is a phospholipid that plays a significant role in oncogenic transformation, tumor growth, angiogenesis, metastasis, and pro-inflammatory processes. Binding of PAF to the PAF-receptor (PAFR) stimulates numerous signal transduction pathways including phospholipase C, D, A2, mitogen-activated protein kinases (MAPKs), and the phosphatidylinositol-calcium second messenger system. Following PAFR activation, cells become rapidly desensitized and this refractory state is dependent on PAFR phosphorylation, internalization, and down-regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":28147166,"end":28193936,"strand":-1,"description":"platelet activating factor receptor [Source:HGNC Symbol;Acc:HGNC:9582]"}, {"versioned_ensembl_gene_id":"ENSG00000161055.3","gene_symbol":"SCGB3A1","gene_name":"secretoglobin family 3A member 1 [Source:HGNC Symbol;Acc:HGNC:18384]","synonyms":"UGRP2,PnSP-2,LU105,HIN1,HIN-1","biotype":"protein_coding","ncbi_id":"92304","summary":null,"start":180590103,"end":180591540,"strand":-1,"description":"secretoglobin family 3A member 1 [Source:HGNC Symbol;Acc:HGNC:18384]"}, {"versioned_ensembl_gene_id":"ENSG00000259577.1","gene_symbol":"CERNA1","gene_name":"competing endogenous lncRNA 1 for miR-4707-5p and miR-4767 [Source:HGNC Symbol;Acc:HGNC:52664]","synonyms":"LOC100129973","biotype":"lincRNA","ncbi_id":"100129973","summary":null,"start":52180093,"end":52205874,"strand":1,"description":"competing endogenous lncRNA 1 for miR-4707-5p and miR-4767 [Source:HGNC Symbol;Acc:HGNC:52664]"}, {"versioned_ensembl_gene_id":"ENSG00000220311.1","gene_symbol":"AL133475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79964215,"end":79964519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218582.2","gene_symbol":"GAPDHP63","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:4157]","synonyms":"GAPDHL8,GAPDL8","biotype":"processed_pseudogene","ncbi_id":"442231","summary":null,"start":79953005,"end":79954011,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:4157]"}, {"versioned_ensembl_gene_id":"ENSG00000248715.2","gene_symbol":"AC105424.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131540281,"end":131540489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267550.1","gene_symbol":"AC022517.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5178119,"end":5178464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231396.2","gene_symbol":"USP17L10","gene_name":"ubiquitin specific peptidase 17-like family member 10 [Source:HGNC Symbol;Acc:HGNC:44438]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287144","summary":null,"start":9210657,"end":9212608,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 10 [Source:HGNC Symbol;Acc:HGNC:44438]"}, {"versioned_ensembl_gene_id":"ENSG00000279667.1","gene_symbol":"AL603839.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40473055,"end":40474059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263748.1","gene_symbol":"EXOGP1","gene_name":"endo/exonuclease (5'-3'), endonuclease G-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44547]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128324","summary":null,"start":21182503,"end":21183499,"strand":-1,"description":"endo/exonuclease (5'-3'), endonuclease G-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44547]"}, {"versioned_ensembl_gene_id":"ENSG00000233196.2","gene_symbol":"AL096803.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":186580515,"end":186581191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145734.18","gene_symbol":"BDP1","gene_name":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]","synonyms":"KIAA1241,TFIIIB90,HSA238520,TFIIIB150,TFC5,TAF3B1,KIAA1689,TFNR","biotype":"protein_coding","ncbi_id":"55814","summary":"The product of this gene is a subunit of the TFIIIB transcription initiation complex, which recruits RNA polymerase III to target promoters in order to initiate transcription. The encoded protein localizes to concentrated aggregates in the nucleus, and is required for transcription from all three types of polymerase III promoters. It is phosphorylated by casein kinase II during mitosis, resulting in its release from chromatin and suppression of polymerase III transcription. [provided by RefSeq, Jul 2008]","start":71455615,"end":71567820,"strand":1,"description":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]"}, {"versioned_ensembl_gene_id":"ENSG00000226119.1","gene_symbol":"Z80107.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102006883,"end":102007294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207524.1","gene_symbol":"RNU6-33P","gene_name":"RNA, U6 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:34277]","synonyms":"RNU6-33","biotype":"snRNA","ncbi_id":"100873748","summary":null,"start":88684848,"end":88684954,"strand":-1,"description":"RNA, U6 small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:34277]"}, {"versioned_ensembl_gene_id":"ENSG00000284015.1","gene_symbol":"MIR1281","gene_name":"microRNA 1281 [Source:HGNC Symbol;Acc:HGNC:35359]","synonyms":"MIRN1281,hsa-mir-1281","biotype":"miRNA","ncbi_id":"100302237","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41092513,"end":41092566,"strand":1,"description":"microRNA 1281 [Source:HGNC Symbol;Acc:HGNC:35359]"}, {"versioned_ensembl_gene_id":"ENSG00000275605.1","gene_symbol":"AC012314.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276769.1","gene_symbol":"MIR6752","gene_name":"microRNA 6752 [Source:HGNC Symbol;Acc:HGNC:50020]","synonyms":"hsa-mir-6752","biotype":"miRNA","ncbi_id":"102465450","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67490245,"end":67490315,"strand":1,"description":"microRNA 6752 [Source:HGNC Symbol;Acc:HGNC:50020]"}, {"versioned_ensembl_gene_id":"ENSG00000221585.1","gene_symbol":"MIR1226","gene_name":"microRNA 1226 [Source:HGNC Symbol;Acc:HGNC:33922]","synonyms":"MIRN1226,hsa-mir-1226","biotype":"miRNA","ncbi_id":"100302232","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47849555,"end":47849629,"strand":1,"description":"microRNA 1226 [Source:HGNC Symbol;Acc:HGNC:33922]"}, {"versioned_ensembl_gene_id":"ENSG00000275981.1","gene_symbol":"AC018816.2","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":4750333,"end":4750685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252510.1","gene_symbol":"RNA5SP55","gene_name":"RNA, 5S ribosomal pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:42832]","synonyms":"RN5S55","biotype":"rRNA","ncbi_id":"100873293","summary":null,"start":116962347,"end":116962471,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:42832]"}, {"versioned_ensembl_gene_id":"ENSG00000274887.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000240474.3","gene_symbol":"RN7SL116P","gene_name":"RNA, 7SL, cytoplasmic 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:46132]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480488","summary":null,"start":38872770,"end":38873074,"strand":1,"description":"RNA, 7SL, cytoplasmic 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:46132]"}, {"versioned_ensembl_gene_id":"ENSG00000252475.1","gene_symbol":"RNU6-1332P","gene_name":"RNA, U6 small nuclear 1332, pseudogene [Source:HGNC Symbol;Acc:HGNC:48295]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480660","summary":null,"start":44962830,"end":44962933,"strand":1,"description":"RNA, U6 small nuclear 1332, pseudogene [Source:HGNC Symbol;Acc:HGNC:48295]"}, {"versioned_ensembl_gene_id":"ENSG00000238410.1","gene_symbol":"snoU109","gene_name":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":75489576,"end":75489710,"strand":1,"description":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]"}, {"versioned_ensembl_gene_id":"ENSG00000212599.1","gene_symbol":"RNU6-279P","gene_name":"RNA, U6 small nuclear 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:47242]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479690","summary":null,"start":59369051,"end":59369151,"strand":-1,"description":"RNA, U6 small nuclear 279, pseudogene [Source:HGNC Symbol;Acc:HGNC:47242]"}, {"versioned_ensembl_gene_id":"ENSG00000201616.1","gene_symbol":"RNU1-91P","gene_name":"RNA, U1 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:48433]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480179","summary":null,"start":3048359,"end":3048521,"strand":-1,"description":"RNA, U1 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:48433]"}, {"versioned_ensembl_gene_id":"ENSG00000277396.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47383160,"end":47383421,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000264704.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32518027,"end":32518174,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000207289.1","gene_symbol":"RNU6-1235P","gene_name":"RNA, U6 small nuclear 1235, pseudogene [Source:HGNC Symbol;Acc:HGNC:48198]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480701","summary":null,"start":21307749,"end":21307855,"strand":1,"description":"RNA, U6 small nuclear 1235, pseudogene [Source:HGNC Symbol;Acc:HGNC:48198]"}, {"versioned_ensembl_gene_id":"ENSG00000209645.1","gene_symbol":"SNORD105","gene_name":"small nucleolar RNA, C/D box 105 [Source:HGNC Symbol;Acc:HGNC:32769]","synonyms":"U105","biotype":"snoRNA","ncbi_id":"692229","summary":null,"start":10107651,"end":10107735,"strand":1,"description":"small nucleolar RNA, C/D box 105 [Source:HGNC Symbol;Acc:HGNC:32769]"}, {"versioned_ensembl_gene_id":"ENSG00000201294.1","gene_symbol":"RNU6-1019P","gene_name":"RNA, U6 small nuclear 1019, pseudogene [Source:HGNC Symbol;Acc:HGNC:47982]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480015","summary":null,"start":3360036,"end":3360142,"strand":1,"description":"RNA, U6 small nuclear 1019, pseudogene [Source:HGNC Symbol;Acc:HGNC:47982]"}, {"versioned_ensembl_gene_id":"ENSG00000199104.2","gene_symbol":"MIR346","gene_name":"microRNA 346 [Source:HGNC Symbol;Acc:HGNC:31780]","synonyms":"hsa-mir-346,MIRN346","biotype":"miRNA","ncbi_id":"442911","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86264694,"end":86264788,"strand":-1,"description":"microRNA 346 [Source:HGNC Symbol;Acc:HGNC:31780]"}, {"versioned_ensembl_gene_id":"ENSG00000222426.1","gene_symbol":"RNU2-50P","gene_name":"RNA, U2 small nuclear 50, pseudogene [Source:HGNC Symbol;Acc:HGNC:48543]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481650","summary":null,"start":34282528,"end":34282670,"strand":-1,"description":"RNA, U2 small nuclear 50, pseudogene [Source:HGNC Symbol;Acc:HGNC:48543]"}, {"versioned_ensembl_gene_id":"ENSG00000274978.1","gene_symbol":"RNU11","gene_name":"RNA, U11 small nuclear [Source:HGNC Symbol;Acc:HGNC:10108]","synonyms":"U11,RNU11-1","biotype":"snRNA","ncbi_id":"26824","summary":null,"start":28648600,"end":28648733,"strand":1,"description":"RNA, U11 small nuclear [Source:HGNC Symbol;Acc:HGNC:10108]"}, {"versioned_ensembl_gene_id":"ENSG00000201330.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29582249,"end":29582332,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000252186.1","gene_symbol":"RNU6-781P","gene_name":"RNA, U6 small nuclear 781, pseudogene [Source:HGNC Symbol;Acc:HGNC:47744]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479911","summary":null,"start":6709452,"end":6709552,"strand":1,"description":"RNA, U6 small nuclear 781, pseudogene [Source:HGNC Symbol;Acc:HGNC:47744]"}, {"versioned_ensembl_gene_id":"ENSG00000207688.2","gene_symbol":"MIR548D2","gene_name":"microRNA 548d-2 [Source:HGNC Symbol;Acc:HGNC:32802]","synonyms":"MIRN548D2,hsa-mir-548d-2","biotype":"miRNA","ncbi_id":"693131","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67471489,"end":67471585,"strand":1,"description":"microRNA 548d-2 [Source:HGNC Symbol;Acc:HGNC:32802]"}, {"versioned_ensembl_gene_id":"ENSG00000200753.1","gene_symbol":"SNORD56","gene_name":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]","synonyms":"U56,RNU56","biotype":"snoRNA","ncbi_id":"26793","summary":null,"start":20377331,"end":20377401,"strand":1,"description":"Small nucleolar RNA SNORD56 [Source:RFAM;Acc:RF00275]"}, {"versioned_ensembl_gene_id":"ENSG00000252183.1","gene_symbol":"RNU6-948P","gene_name":"RNA, U6 small nuclear 948, pseudogene [Source:HGNC Symbol;Acc:HGNC:47911]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481479","summary":null,"start":121192797,"end":121192903,"strand":-1,"description":"RNA, U6 small nuclear 948, pseudogene [Source:HGNC Symbol;Acc:HGNC:47911]"}, {"versioned_ensembl_gene_id":"ENSG00000252562.1","gene_symbol":"RNU6-922P","gene_name":"RNA, U6 small nuclear 922, pseudogene [Source:HGNC Symbol;Acc:HGNC:47885]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479974","summary":null,"start":23613661,"end":23613759,"strand":-1,"description":"RNA, U6 small nuclear 922, pseudogene [Source:HGNC Symbol;Acc:HGNC:47885]"}, {"versioned_ensembl_gene_id":"ENSG00000252329.1","gene_symbol":"SCARNA16","gene_name":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]","synonyms":"ACA47","biotype":"scaRNA","ncbi_id":"677781","summary":null,"start":12904817,"end":12904988,"strand":-1,"description":"Small Cajal body specific RNA 16 [Source:RFAM;Acc:RF00424]"}, {"versioned_ensembl_gene_id":"ENSG00000265083.1","gene_symbol":"MIR3691","gene_name":"microRNA 3691 [Source:HGNC Symbol;Acc:HGNC:38909]","synonyms":"hsa-mir-3691","biotype":"miRNA","ncbi_id":"100500900","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5148233,"end":5148322,"strand":-1,"description":"microRNA 3691 [Source:HGNC Symbol;Acc:HGNC:38909]"}, {"versioned_ensembl_gene_id":"ENSG00000201140.1","gene_symbol":"RN7SKP128","gene_name":"RNA, 7SK small nuclear pseudogene 128 [Source:HGNC Symbol;Acc:HGNC:45852]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479151","summary":null,"start":117197118,"end":117197420,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 128 [Source:HGNC Symbol;Acc:HGNC:45852]"}, {"versioned_ensembl_gene_id":"ENSG00000252185.1","gene_symbol":"RNU6-752P","gene_name":"RNA, U6 small nuclear 752, pseudogene [Source:HGNC Symbol;Acc:HGNC:47715]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481417","summary":null,"start":126755316,"end":126755417,"strand":-1,"description":"RNA, U6 small nuclear 752, pseudogene [Source:HGNC Symbol;Acc:HGNC:47715]"}, {"versioned_ensembl_gene_id":"ENSG00000200183.1","gene_symbol":"RNU6-238P","gene_name":"RNA, U6 small nuclear 238, pseudogene [Source:HGNC Symbol;Acc:HGNC:47201]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481253","summary":null,"start":50656973,"end":50657078,"strand":1,"description":"RNA, U6 small nuclear 238, pseudogene [Source:HGNC Symbol;Acc:HGNC:47201]"}, {"versioned_ensembl_gene_id":"ENSG00000251829.1","gene_symbol":"RNA5SP436","gene_name":"RNA, 5S ribosomal pseudogene 436 [Source:HGNC Symbol;Acc:HGNC:43336]","synonyms":"RN5S436","biotype":"rRNA","ncbi_id":"100873685","summary":null,"start":15782341,"end":15782455,"strand":1,"description":"RNA, 5S ribosomal pseudogene 436 [Source:HGNC Symbol;Acc:HGNC:43336]"}, {"versioned_ensembl_gene_id":"ENSG00000212539.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":56957270,"end":56957469,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000265996.1","gene_symbol":"MIR3671","gene_name":"microRNA 3671 [Source:HGNC Symbol;Acc:HGNC:38925]","synonyms":"hsa-mir-3671","biotype":"miRNA","ncbi_id":"100500854","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65057755,"end":65057842,"strand":-1,"description":"microRNA 3671 [Source:HGNC Symbol;Acc:HGNC:38925]"}, {"versioned_ensembl_gene_id":"ENSG00000200224.2","gene_symbol":"RNU6-626P","gene_name":"RNA, U6 small nuclear 626, pseudogene [Source:HGNC Symbol;Acc:HGNC:47589]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481379","summary":null,"start":56945730,"end":56945836,"strand":1,"description":"RNA, U6 small nuclear 626, pseudogene [Source:HGNC Symbol;Acc:HGNC:47589]"}, {"versioned_ensembl_gene_id":"ENSG00000223287.1","gene_symbol":"RNU6-954P","gene_name":"RNA, U6 small nuclear 954, pseudogene [Source:HGNC Symbol;Acc:HGNC:47917]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481481","summary":null,"start":13968489,"end":13968595,"strand":-1,"description":"RNA, U6 small nuclear 954, pseudogene [Source:HGNC Symbol;Acc:HGNC:47917]"}, {"versioned_ensembl_gene_id":"ENSG00000202310.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100158868,"end":100158975,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200086.1","gene_symbol":"RNU6-433P","gene_name":"RNA, U6 small nuclear 433, pseudogene [Source:HGNC Symbol;Acc:HGNC:47396]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481315","summary":null,"start":55014418,"end":55014521,"strand":-1,"description":"RNA, U6 small nuclear 433, pseudogene [Source:HGNC Symbol;Acc:HGNC:47396]"}, {"versioned_ensembl_gene_id":"ENSG00000202399.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97772313,"end":97772425,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284370.1","gene_symbol":"MIR4640","gene_name":"microRNA 4640 [Source:HGNC Symbol;Acc:HGNC:41561]","synonyms":"hsa-mir-4640","biotype":"miRNA","ncbi_id":"100616237","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30890883,"end":30890972,"strand":1,"description":"microRNA 4640 [Source:HGNC Symbol;Acc:HGNC:41561]"}, {"versioned_ensembl_gene_id":"ENSG00000265160.1","gene_symbol":"MIR5003","gene_name":"microRNA 5003 [Source:HGNC Symbol;Acc:HGNC:43512]","synonyms":"hsa-mir-5003","biotype":"miRNA","ncbi_id":"100847029","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":172662165,"end":172662263,"strand":1,"description":"microRNA 5003 [Source:HGNC Symbol;Acc:HGNC:43512]"}, {"versioned_ensembl_gene_id":"ENSG00000283871.1","gene_symbol":"MIR130B","gene_name":"microRNA 130b [Source:HGNC Symbol;Acc:HGNC:31515]","synonyms":"MIRN130B,hsa-mir-130b,MIRN130B,hsa-mir-130b","biotype":"miRNA","ncbi_id":"406920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21653304,"end":21653385,"strand":1,"description":"microRNA 130b [Source:HGNC Symbol;Acc:HGNC:31515]"}, {"versioned_ensembl_gene_id":"ENSG00000278502.1","gene_symbol":"MIR6082","gene_name":"microRNA 6082 [Source:HGNC Symbol;Acc:HGNC:49984]","synonyms":"hsa-mir-6082","biotype":"miRNA","ncbi_id":"102466953","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":171186184,"end":171186292,"strand":1,"description":"microRNA 6082 [Source:HGNC Symbol;Acc:HGNC:49984]"}, {"versioned_ensembl_gene_id":"ENSG00000200254.1","gene_symbol":"RNU6-536P","gene_name":"RNA, U6 small nuclear 536, pseudogene [Source:HGNC Symbol;Acc:HGNC:47499]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481350","summary":null,"start":42569033,"end":42569139,"strand":1,"description":"RNA, U6 small nuclear 536, pseudogene [Source:HGNC Symbol;Acc:HGNC:47499]"}, {"versioned_ensembl_gene_id":"ENSG00000263556.2","gene_symbol":"RN7SL383P","gene_name":"RNA, 7SL, cytoplasmic 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:46399]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479363","summary":null,"start":44716193,"end":44716486,"strand":1,"description":"RNA, 7SL, cytoplasmic 383, pseudogene [Source:HGNC Symbol;Acc:HGNC:46399]"}, {"versioned_ensembl_gene_id":"ENSG00000277630.4","gene_symbol":"BX072566.1","gene_name":"uncharacterized protein LOC100288966 [Source:RefSeq peptide;Acc:NP_001244291]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":108007,"end":139659,"strand":-1,"description":"uncharacterized protein LOC100288966 [Source:RefSeq peptide;Acc:NP_001244291]"}, {"versioned_ensembl_gene_id":"ENSG00000222448.1","gene_symbol":"RN7SKP150","gene_name":"RNA, 7SK small nuclear pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:45874]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480880","summary":null,"start":179845832,"end":179846152,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:45874]"}, {"versioned_ensembl_gene_id":"ENSG00000266232.1","gene_symbol":"MIR3178","gene_name":"microRNA 3178 [Source:HGNC Symbol;Acc:HGNC:38381]","synonyms":"hsa-mir-3178","biotype":"miRNA","ncbi_id":"100422974","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2531922,"end":2532005,"strand":-1,"description":"microRNA 3178 [Source:HGNC Symbol;Acc:HGNC:38381]"}, {"versioned_ensembl_gene_id":"ENSG00000264397.1","gene_symbol":"MIR3180-5","gene_name":"microRNA 3180-5 [Source:HGNC Symbol;Acc:HGNC:38969]","synonyms":"hsa-mir-3180-5","biotype":"miRNA","ncbi_id":"100500916","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2135977,"end":2136129,"strand":-1,"description":"microRNA 3180-5 [Source:HGNC Symbol;Acc:HGNC:38969]"}, {"versioned_ensembl_gene_id":"ENSG00000264266.1","gene_symbol":"MIR4322","gene_name":"microRNA 4322 [Source:HGNC Symbol;Acc:HGNC:38261]","synonyms":"hsa-mir-4322","biotype":"miRNA","ncbi_id":"100422925","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10230413,"end":10230485,"strand":1,"description":"microRNA 4322 [Source:HGNC Symbol;Acc:HGNC:38261]"}, {"versioned_ensembl_gene_id":"ENSG00000216179.1","gene_symbol":"MIR541","gene_name":"microRNA 541 [Source:HGNC Symbol;Acc:HGNC:33650]","synonyms":"MIRN541,hsa-mir-541","biotype":"miRNA","ncbi_id":"100126308","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101064495,"end":101064578,"strand":1,"description":"microRNA 541 [Source:HGNC Symbol;Acc:HGNC:33650]"}, {"versioned_ensembl_gene_id":"ENSG00000273758.1","gene_symbol":"MIR6790","gene_name":"microRNA 6790 [Source:HGNC Symbol;Acc:HGNC:50161]","synonyms":"hsa-mir-6790","biotype":"miRNA","ncbi_id":"102465473","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6392921,"end":6392983,"strand":-1,"description":"microRNA 6790 [Source:HGNC Symbol;Acc:HGNC:50161]"}, {"versioned_ensembl_gene_id":"ENSG00000284293.1","gene_symbol":"MIR7113","gene_name":"microRNA 7113 [Source:HGNC Symbol;Acc:HGNC:49947]","synonyms":"hsa-mir-7113","biotype":"miRNA","ncbi_id":"102465669","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68032864,"end":68032922,"strand":1,"description":"microRNA 7113 [Source:HGNC Symbol;Acc:HGNC:49947]"}, {"versioned_ensembl_gene_id":"ENSG00000207410.1","gene_symbol":"SNORA8","gene_name":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]","synonyms":"ACA8","biotype":"snoRNA","ncbi_id":"654320","summary":null,"start":67271469,"end":67271607,"strand":1,"description":"Small nucleolar RNA SNORA8 [Source:RFAM;Acc:RF00393]"}, {"versioned_ensembl_gene_id":"ENSG00000201709.1","gene_symbol":"RNU6-686P","gene_name":"RNA, U6 small nuclear 686, pseudogene [Source:HGNC Symbol;Acc:HGNC:47649]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481397","summary":null,"start":65229861,"end":65229967,"strand":1,"description":"RNA, U6 small nuclear 686, pseudogene [Source:HGNC Symbol;Acc:HGNC:47649]"}, {"versioned_ensembl_gene_id":"ENSG00000201308.1","gene_symbol":"RNU6-512P","gene_name":"RNA, U6 small nuclear 512, pseudogene [Source:HGNC Symbol;Acc:HGNC:47475]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480394","summary":null,"start":135656477,"end":135656579,"strand":-1,"description":"RNA, U6 small nuclear 512, pseudogene [Source:HGNC Symbol;Acc:HGNC:47475]"}, {"versioned_ensembl_gene_id":"ENSG00000272113.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32820261,"end":32820350,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283929.1","gene_symbol":"MIR5010","gene_name":"microRNA 5010 [Source:HGNC Symbol;Acc:HGNC:43484]","synonyms":"hsa-mir-5010","biotype":"miRNA","ncbi_id":"100847046","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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{"versioned_ensembl_gene_id":"ENSG00000271814.1","gene_symbol":"RN7SKP290","gene_name":"RNA, 7SK small nuclear pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:46014]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480480","summary":null,"start":12614003,"end":12614197,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 290 [Source:HGNC Symbol;Acc:HGNC:46014]"}, {"versioned_ensembl_gene_id":"ENSG00000221564.1","gene_symbol":"RNU6ATAC42P","gene_name":"RNA, U6atac small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46941]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481173","summary":null,"start":64939023,"end":64939117,"strand":1,"description":"RNA, U6atac small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46941]"}, {"versioned_ensembl_gene_id":"ENSG00000200436.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112661657,"end":112661768,"strand":1,"description":"Y RNA 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51692612,"end":51692681,"strand":1,"description":"microRNA 99b [Source:HGNC Symbol;Acc:HGNC:31651]"}, {"versioned_ensembl_gene_id":"ENSG00000283867.1","gene_symbol":"MIR1307","gene_name":"microRNA 1307 [Source:HGNC Symbol;Acc:HGNC:35372]","synonyms":"MIRN1307,hsa-mir-1307","biotype":"miRNA","ncbi_id":"100302174","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112634170,"end":112634254,"strand":1,"description":"microRNA 4295 [Source:HGNC Symbol;Acc:HGNC:38220]"}, {"versioned_ensembl_gene_id":"ENSG00000252274.1","gene_symbol":"SCARNA24","gene_name":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]","synonyms":null,"biotype":"scaRNA","ncbi_id":null,"summary":null,"start":72818836,"end":72818972,"strand":-1,"description":"Small Cajal body specific RNA 24 [Source:RFAM;Acc:RF00422]"}, {"versioned_ensembl_gene_id":"ENSG00000277510.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40450225,"end":40450480,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201825.1","gene_symbol":"RNU6-1131P","gene_name":"RNA, U6 small nuclear 1131, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207386.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206025593,"end":206025697,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000244534.3","gene_symbol":"RN7SL211P","gene_name":"RNA, 7SL, cytoplasmic 211, pseudogene [Source:HGNC Symbol;Acc:HGNC:46227]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479299","summary":null,"start":64906863,"end":64907138,"strand":-1,"description":"RNA, 7SL, cytoplasmic 211, pseudogene [Source:HGNC Symbol;Acc:HGNC:46227]"}, {"versioned_ensembl_gene_id":"ENSG00000201041.1","gene_symbol":"RNA5SP242","gene_name":"RNA, 5S ribosomal pseudogene 242 [Source:HGNC Symbol;Acc:HGNC:43142]","synonyms":"RN5S242","biotype":"rRNA","ncbi_id":"100873500","summary":null,"start":128697439,"end":128697556,"strand":1,"description":"RNA, 5S ribosomal pseudogene 242 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000264857.1","gene_symbol":"MIR5696","gene_name":"microRNA 5696 [Source:HGNC Symbol;Acc:HGNC:43516]","synonyms":"hsa-mir-5696","biotype":"miRNA","ncbi_id":"100847007","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101309450,"end":101309534,"strand":1,"description":"microRNA 5696 [Source:HGNC Symbol;Acc:HGNC:43516]"}, {"versioned_ensembl_gene_id":"ENSG00000252816.1","gene_symbol":"RNA5SP337","gene_name":"RNA, 5S ribosomal pseudogene 337 [Source:HGNC Symbol;Acc:HGNC:43237]","synonyms":"RN5S337","biotype":"rRNA","ncbi_id":"100873600","summary":null,"start":21383801,"end":21383909,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 337 [Source:HGNC Symbol;Acc:HGNC:43237]"}, {"versioned_ensembl_gene_id":"ENSG00000207810.1","gene_symbol":"MIR519E","gene_name":"microRNA 519e [Source:HGNC Symbol;Acc:HGNC:32095]","synonyms":"MIRN519E,hsa-mir-519e","biotype":"miRNA","ncbi_id":"574463","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53679940,"end":53680023,"strand":1,"description":"microRNA 519e [Source:HGNC Symbol;Acc:HGNC:32095]"}, {"versioned_ensembl_gene_id":"ENSG00000284172.1","gene_symbol":"MIR4315-2","gene_name":"microRNA 4315-2 [Source:HGNC Symbol;Acc:HGNC:38356]","synonyms":"hsa-mir-4315-2","biotype":"miRNA","ncbi_id":"100422961","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64822030,"end":64822102,"strand":-1,"description":"microRNA 4315-2 [Source:HGNC Symbol;Acc:HGNC:38356]"}, {"versioned_ensembl_gene_id":"ENSG00000238531.1","gene_symbol":"SNORD105B","gene_name":"small nucleolar RNA, C/D box 105B [Source:HGNC Symbol;Acc:HGNC:33572]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113382","summary":null,"start":10109757,"end":10109835,"strand":1,"description":"small nucleolar RNA, C/D box 105B [Source:HGNC Symbol;Acc:HGNC:33572]"}, {"versioned_ensembl_gene_id":"ENSG00000221036.5","gene_symbol":"MIR1193","gene_name":"microRNA 1193 [Source:HGNC Symbol;Acc:HGNC:38247]","synonyms":"hsa-mir-1193","biotype":"miRNA","ncbi_id":"100422837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101030052,"end":101030129,"strand":1,"description":"microRNA 1193 [Source:HGNC Symbol;Acc:HGNC:38247]"}, {"versioned_ensembl_gene_id":"ENSG00000281825.1","gene_symbol":"AL355480.4","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":45605657,"end":45605730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240160.3","gene_symbol":"RN7SL263P","gene_name":"RNA, 7SL, cytoplasmic 263, pseudogene [Source:HGNC Symbol;Acc:HGNC:46279]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480993","summary":null,"start":23261782,"end":23262071,"strand":-1,"description":"RNA, 7SL, cytoplasmic 263, pseudogene [Source:HGNC Symbol;Acc:HGNC:46279]"}, {"versioned_ensembl_gene_id":"ENSG00000202200.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128761717,"end":128761808,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284360.1","gene_symbol":"MIR6125","gene_name":"microRNA 6125 [Source:HGNC Symbol;Acc:HGNC:49931]","synonyms":"hsa-mir-6125","biotype":"miRNA","ncbi_id":"102465133","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62260359,"end":62260454,"strand":1,"description":"microRNA 6125 [Source:HGNC Symbol;Acc:HGNC:49931]"}, {"versioned_ensembl_gene_id":"ENSG00000202269.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":15110786,"end":15110920,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000207252.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":24455911,"end":24456010,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277733.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000201346.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":3384229,"end":3384440,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000207422.1","gene_symbol":"RNU6-813P","gene_name":"RNA, U6 small nuclear 813, pseudogene [Source:HGNC Symbol;Acc:HGNC:47776]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481438","summary":null,"start":151615773,"end":151615879,"strand":-1,"description":"RNA, U6 small nuclear 813, pseudogene [Source:HGNC Symbol;Acc:HGNC:47776]"}, {"versioned_ensembl_gene_id":"ENSG00000200822.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":222404985,"end":222405095,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212134.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":31376319,"end":31376446,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000199780.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":59533786,"end":59533898,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222675.1","gene_symbol":"RNA5SP146","gene_name":"RNA, 5S ribosomal pseudogene 146 [Source:HGNC Symbol;Acc:HGNC:43046]","synonyms":"RN5S146","biotype":"rRNA","ncbi_id":"100873413","summary":null,"start":157173918,"end":157174040,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 146 [Source:HGNC Symbol;Acc:HGNC:43046]"}, {"versioned_ensembl_gene_id":"ENSG00000212344.1","gene_symbol":"RNU6-823P","gene_name":"RNA, U6 small nuclear 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:47786]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481441","summary":null,"start":128141875,"end":128141977,"strand":-1,"description":"RNA, U6 small nuclear 823, pseudogene [Source:HGNC Symbol;Acc:HGNC:47786]"}, {"versioned_ensembl_gene_id":"ENSG00000207827.1","gene_symbol":"MIR30A","gene_name":"microRNA 30a [Source:HGNC Symbol;Acc:HGNC:31624]","synonyms":"hsa-mir-30a,MIRN30A","biotype":"miRNA","ncbi_id":"407029","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The encoded miRNA is one of five members of the miR-30 family of highly conserved miRNAs and participates in many cellular processes. It has additionally been implicated in the development of several types of cancer. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2017]","start":71403551,"end":71403621,"strand":-1,"description":"microRNA 30a [Source:HGNC Symbol;Acc:HGNC:31624]"}, {"versioned_ensembl_gene_id":"ENSG00000274582.1","gene_symbol":"SNORA16A","gene_name":"small nucleolar RNA, H/ACA box 16A [Source:HGNC Symbol;Acc:HGNC:32605]","synonyms":"ACA16,ACA16","biotype":"snoRNA","ncbi_id":"692073","summary":null,"start":28580920,"end":28581056,"strand":-1,"description":"small nucleolar RNA, H/ACA box 16A [Source:HGNC Symbol;Acc:HGNC:32605]"}, {"versioned_ensembl_gene_id":"ENSG00000277759.1","gene_symbol":"MIR6719","gene_name":"microRNA 6719 [Source:HGNC Symbol;Acc:HGNC:50012]","synonyms":"hsa-mir-6719","biotype":"miRNA","ncbi_id":"102465974","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39829716,"end":39829802,"strand":-1,"description":"microRNA 6719 [Source:HGNC Symbol;Acc:HGNC:50012]"}, {"versioned_ensembl_gene_id":"ENSG00000200312.1","gene_symbol":"RN7SKP255","gene_name":"RNA, 7SK small nuclear pseudogene 255 [Source:HGNC Symbol;Acc:HGNC:45979]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479209","summary":null,"start":89712511,"end":89712823,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 255 [Source:HGNC Symbol;Acc:HGNC:45979]"}, {"versioned_ensembl_gene_id":"ENSG00000207505.1","gene_symbol":"RNU6-1105P","gene_name":"RNA, U6 small nuclear 1105, pseudogene [Source:HGNC Symbol;Acc:HGNC:48068]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480052","summary":null,"start":186771841,"end":186771947,"strand":-1,"description":"RNA, U6 small nuclear 1105, pseudogene [Source:HGNC Symbol;Acc:HGNC:48068]"}, {"versioned_ensembl_gene_id":"ENSG00000277754.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":101145480,"end":101145695,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000276774.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000276083.1","gene_symbol":"MIR7976","gene_name":"microRNA 7976 [Source:HGNC Symbol;Acc:HGNC:50092]","synonyms":"hsa-mir-7976","biotype":"miRNA","ncbi_id":"102465857","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127587111,"end":127587176,"strand":-1,"description":"microRNA 7976 [Source:HGNC Symbol;Acc:HGNC:50092]"}, {"versioned_ensembl_gene_id":"ENSG00000206936.1","gene_symbol":"RNU4-52P","gene_name":"RNA, U4 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:46988]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481188","summary":null,"start":49082028,"end":49082165,"strand":1,"description":"RNA, U4 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:46988]"}, {"versioned_ensembl_gene_id":"ENSG00000277943.4","gene_symbol":"CCL4","gene_name":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]","synonyms":"SCYA4,SCYA4,MIP-1-beta,MIP-1-beta,LAG1,LAG1,AT744.1,AT744.1,Act-2,Act-2","biotype":"protein_coding","ncbi_id":"6351","summary":"The protein encoded by this gene is a mitogen-inducible monokine and is one of the major HIV-suppressive factors produced by CD8+ T-cells. The encoded protein is secreted and has chemokinetic and inflammatory functions. [provided by RefSeq, Dec 2012]","start":36103827,"end":36105621,"strand":1,"description":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]"}, {"versioned_ensembl_gene_id":"ENSG00000275842.1","gene_symbol":"MIR941-5","gene_name":"microRNA 941-5 [Source:HGNC Symbol;Acc:HGNC:50845]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504732","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919868,"end":63919939,"strand":1,"description":"microRNA 941-5 [Source:HGNC Symbol;Acc:HGNC:50845]"}, {"versioned_ensembl_gene_id":"ENSG00000216191.1","gene_symbol":"MIR8485","gene_name":"microRNA 8485 [Source:HGNC Symbol;Acc:HGNC:50839]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504737","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50696172,"end":50696262,"strand":-1,"description":"microRNA 8485 [Source:HGNC Symbol;Acc:HGNC:50839]"}, {"versioned_ensembl_gene_id":"ENSG00000278287.1","gene_symbol":"DLEU2_5","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63549133,"end":63549216,"strand":-1,"description":"Deleted in lymphocytic leukemia 2 conserved region 5 [Source:RFAM;Acc:RF02109]"}, {"versioned_ensembl_gene_id":"ENSG00000200213.1","gene_symbol":"RNU6-992P","gene_name":"RNA, U6 small nuclear 992, pseudogene [Source:HGNC Symbol;Acc:HGNC:47955]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481493","summary":null,"start":36066545,"end":36066652,"strand":1,"description":"RNA, U6 small nuclear 992, pseudogene [Source:HGNC Symbol;Acc:HGNC:47955]"}, {"versioned_ensembl_gene_id":"ENSG00000264274.1","gene_symbol":"MIR4799","gene_name":"microRNA 4799 [Source:HGNC Symbol;Acc:HGNC:41584]","synonyms":"hsa-mir-4799","biotype":"miRNA","ncbi_id":"100616246","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147782595,"end":147782668,"strand":1,"description":"microRNA 4799 [Source:HGNC Symbol;Acc:HGNC:41584]"}, {"versioned_ensembl_gene_id":"ENSG00000252005.2","gene_symbol":"RNU4ATAC8P","gene_name":"RNA, U4atac small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:46894]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481157","summary":null,"start":73883714,"end":73883822,"strand":1,"description":"RNA, U4atac small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:46894]"}, {"versioned_ensembl_gene_id":"ENSG00000277184.1","gene_symbol":"SNORA9","gene_name":"small nucleolar RNA, H/ACA box 9 [Source:HGNC Symbol;Acc:HGNC:32597]","synonyms":"ACA9,SNORA9A","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":44985378,"end":44985510,"strand":-1,"description":"small nucleolar RNA, H/ACA box 9 [Source:HGNC Symbol;Acc:HGNC:32597]"}, {"versioned_ensembl_gene_id":"ENSG00000277784.1","gene_symbol":"MIR6786","gene_name":"microRNA 6786 [Source:HGNC Symbol;Acc:HGNC:49970]","synonyms":"hsa-mir-6786","biotype":"miRNA","ncbi_id":"102465471","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81693757,"end":81693869,"strand":1,"description":"microRNA 6786 [Source:HGNC Symbol;Acc:HGNC:49970]"}, {"versioned_ensembl_gene_id":"ENSG00000199601.1","gene_symbol":"RNU6-562P","gene_name":"RNA, U6 small nuclear 562, pseudogene [Source:HGNC Symbol;Acc:HGNC:47525]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479816","summary":null,"start":75202703,"end":75202809,"strand":1,"description":"RNA, U6 small nuclear 562, pseudogene [Source:HGNC Symbol;Acc:HGNC:47525]"}, {"versioned_ensembl_gene_id":"ENSG00000206954.1","gene_symbol":"RNU6-1201P","gene_name":"RNA, U6 small nuclear 1201, pseudogene [Source:HGNC Symbol;Acc:HGNC:48164]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481942","summary":null,"start":48088678,"end":48088784,"strand":-1,"description":"RNA, U6 small nuclear 1201, pseudogene [Source:HGNC Symbol;Acc:HGNC:48164]"}, {"versioned_ensembl_gene_id":"ENSG00000274662.1","gene_symbol":"RN7SKP236","gene_name":"RNA, 7SK small nuclear pseudogene 236 [Source:HGNC Symbol;Acc:HGNC:45960]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480906","summary":null,"start":25101132,"end":25101415,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 236 [Source:HGNC Symbol;Acc:HGNC:45960]"}, {"versioned_ensembl_gene_id":"ENSG00000265123.2","gene_symbol":"RN7SL200P","gene_name":"RNA, 7SL, cytoplasmic 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:46216]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480976","summary":null,"start":34685355,"end":34685642,"strand":-1,"description":"RNA, 7SL, cytoplasmic 200, pseudogene [Source:HGNC Symbol;Acc:HGNC:46216]"}, {"versioned_ensembl_gene_id":"ENSG00000251956.1","gene_symbol":"RNU6-617P","gene_name":"RNA, U6 small nuclear 617, pseudogene [Source:HGNC Symbol;Acc:HGNC:47580]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479839","summary":null,"start":131602790,"end":131602896,"strand":1,"description":"RNA, U6 small nuclear 617, pseudogene [Source:HGNC Symbol;Acc:HGNC:47580]"}, {"versioned_ensembl_gene_id":"ENSG00000276588.1","gene_symbol":"RN7SL322P","gene_name":"RNA, 7SL, cytoplasmic 322, pseudogene [Source:HGNC Symbol;Acc:HGNC:46338]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479340","summary":null,"start":47581023,"end":47581321,"strand":1,"description":"RNA, 7SL, cytoplasmic 322, pseudogene [Source:HGNC Symbol;Acc:HGNC:46338]"}, {"versioned_ensembl_gene_id":"ENSG00000263897.1","gene_symbol":"MIR4669","gene_name":"microRNA 4669 [Source:HGNC Symbol;Acc:HGNC:41558]","synonyms":"hsa-mir-4669","biotype":"miRNA","ncbi_id":"100616236","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134379411,"end":134379472,"strand":1,"description":"microRNA 4669 [Source:HGNC Symbol;Acc:HGNC:41558]"}, {"versioned_ensembl_gene_id":"ENSG00000265658.6","gene_symbol":"MIR3690","gene_name":"microRNA 3690 [Source:HGNC Symbol;Acc:HGNC:38967]","synonyms":"MIR3690-2,MIR3690-1,hsa-mir-3690-2,hsa-mir-3690","biotype":"miRNA","ncbi_id":"100500894","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1293918,"end":1293992,"strand":1,"description":"microRNA 3690 [Source:HGNC Symbol;Acc:HGNC:38967]"}, {"versioned_ensembl_gene_id":"ENSG00000222459.1","gene_symbol":"RNA5SP293","gene_name":"RNA, 5S ribosomal pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:43193]","synonyms":"RN5S293","biotype":"rRNA","ncbi_id":"100873546","summary":null,"start":107918866,"end":107918978,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 293 [Source:HGNC Symbol;Acc:HGNC:43193]"}, {"versioned_ensembl_gene_id":"ENSG00000252935.1","gene_symbol":"RNU6-1220P","gene_name":"RNA, U6 small nuclear 1220, pseudogene [Source:HGNC Symbol;Acc:HGNC:48183]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481565","summary":null,"start":78398515,"end":78398622,"strand":-1,"description":"RNA, U6 small nuclear 1220, pseudogene [Source:HGNC Symbol;Acc:HGNC:48183]"}, {"versioned_ensembl_gene_id":"ENSG00000240003.2","gene_symbol":"RPL7P24","gene_name":"ribosomal protein L7 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127893","summary":null,"start":80500332,"end":80501400,"strand":1,"description":"ribosomal protein L7 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36715]"}, {"versioned_ensembl_gene_id":"ENSG00000221028.1","gene_symbol":"MIR1231","gene_name":"microRNA 1231 [Source:HGNC Symbol;Acc:HGNC:33921]","synonyms":"MIRN1231,hsa-mir-1231","biotype":"miRNA","ncbi_id":"100302158","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":201808611,"end":201808702,"strand":1,"description":"microRNA 1231 [Source:HGNC Symbol;Acc:HGNC:33921]"}, {"versioned_ensembl_gene_id":"ENSG00000207992.1","gene_symbol":"MIR519A1","gene_name":"microRNA 519a-1 [Source:HGNC Symbol;Acc:HGNC:32128]","synonyms":"MIRN519A1,MIRN519A-1,hsa-mir-519a-1","biotype":"miRNA","ncbi_id":"574496","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53752397,"end":53752481,"strand":1,"description":"microRNA 519a-1 [Source:HGNC Symbol;Acc:HGNC:32128]"}, {"versioned_ensembl_gene_id":"ENSG00000276830.1","gene_symbol":"MIR6730","gene_name":"microRNA 6730 [Source:HGNC Symbol;Acc:HGNC:50222]","synonyms":"hsa-mir-6730","biotype":"miRNA","ncbi_id":"102466722","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12578957,"end":12579023,"strand":-1,"description":"microRNA 6730 [Source:HGNC Symbol;Acc:HGNC:50222]"}, {"versioned_ensembl_gene_id":"ENSG00000207778.3","gene_symbol":"MIR3591","gene_name":"microRNA 3591 [Source:HGNC Symbol;Acc:HGNC:41875]","synonyms":"hsa-mir-3591","biotype":"miRNA","ncbi_id":"100616357","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58451080,"end":58451152,"strand":-1,"description":"microRNA 3591 [Source:HGNC Symbol;Acc:HGNC:41875]"}, {"versioned_ensembl_gene_id":"ENSG00000207752.1","gene_symbol":"MIR199A1","gene_name":"microRNA 199a-1 [Source:HGNC Symbol;Acc:HGNC:31571]","synonyms":"MIRN199A1,hsa-mir-199a-1","biotype":"miRNA","ncbi_id":"406976","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10817426,"end":10817496,"strand":-1,"description":"microRNA 199a-1 [Source:HGNC Symbol;Acc:HGNC:31571]"}, {"versioned_ensembl_gene_id":"ENSG00000238728.1","gene_symbol":"MIR1972-1","gene_name":"microRNA 1972-1 [Source:HGNC Symbol;Acc:HGNC:37060]","synonyms":"MIR1972,hsa-mir-1972","biotype":"miRNA","ncbi_id":"100302243","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15010321,"end":15010397,"strand":-1,"description":"microRNA 1972-1 [Source:HGNC Symbol;Acc:HGNC:37060]"}, {"versioned_ensembl_gene_id":"ENSG00000244264.3","gene_symbol":"RN7SL597P","gene_name":"RNA, 7SL, cytoplasmic 597, pseudogene [Source:HGNC Symbol;Acc:HGNC:46613]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479440","summary":null,"start":41121876,"end":41122171,"strand":1,"description":"RNA, 7SL, cytoplasmic 597, pseudogene [Source:HGNC Symbol;Acc:HGNC:46613]"}, {"versioned_ensembl_gene_id":"ENSG00000207114.1","gene_symbol":"RNU6-348P","gene_name":"RNA, U6 small nuclear 348, pseudogene [Source:HGNC Symbol;Acc:HGNC:47311]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481289","summary":null,"start":171504245,"end":171504351,"strand":-1,"description":"RNA, U6 small nuclear 348, pseudogene [Source:HGNC Symbol;Acc:HGNC:47311]"}, {"versioned_ensembl_gene_id":"ENSG00000201942.1","gene_symbol":"RNA5SP363","gene_name":"RNA, 5S ribosomal pseudogene 363 [Source:HGNC Symbol;Acc:HGNC:43263]","synonyms":"RN5S363","biotype":"rRNA","ncbi_id":"100873622","summary":null,"start":79878305,"end":79878419,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 363 [Source:HGNC Symbol;Acc:HGNC:43263]"}, {"versioned_ensembl_gene_id":"ENSG00000275987.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":30437,"end":30580,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000199130.3","gene_symbol":"MIR365A","gene_name":"microRNA 365a [Source:HGNC Symbol;Acc:HGNC:33692]","synonyms":"MIRN365-1,MIR365-1,hsa-mir-365-1","biotype":"miRNA","ncbi_id":"100126355","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14309285,"end":14309371,"strand":1,"description":"microRNA 365a [Source:HGNC Symbol;Acc:HGNC:33692]"}, {"versioned_ensembl_gene_id":"ENSG00000267200.1","gene_symbol":"MIR132","gene_name":"microRNA 132 [Source:HGNC Symbol;Acc:HGNC:31516]","synonyms":"MIRN132,hsa-mir-132","biotype":"miRNA","ncbi_id":"406921","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2049908,"end":2050008,"strand":-1,"description":"microRNA 132 [Source:HGNC Symbol;Acc:HGNC:31516]"}, {"versioned_ensembl_gene_id":"ENSG00000277030.1","gene_symbol":"MIR8071-2","gene_name":"microRNA 8071-2 [Source:HGNC Symbol;Acc:HGNC:49958]","synonyms":"hsa-mir-8071-2","biotype":"miRNA","ncbi_id":"102466889","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105640168,"end":105640232,"strand":1,"description":"microRNA 8071-2 [Source:HGNC Symbol;Acc:HGNC:49958]"}, {"versioned_ensembl_gene_id":"ENSG00000238570.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":161558544,"end":161558646,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000201806.1","gene_symbol":"RNU4-8P","gene_name":"RNA, U4 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:10195]","synonyms":"U4/14,U4,RNU4P2","biotype":"snRNA","ncbi_id":"6070","summary":null,"start":97664591,"end":97664731,"strand":-1,"description":"RNA, U4 small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:10195]"}, {"versioned_ensembl_gene_id":"ENSG00000241037.3","gene_symbol":"RN7SL335P","gene_name":"RNA, 7SL, cytoplasmic 335, pseudogene [Source:HGNC Symbol;Acc:HGNC:46351]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480375","summary":null,"start":122087508,"end":122087811,"strand":-1,"description":"RNA, 7SL, cytoplasmic 335, pseudogene [Source:HGNC Symbol;Acc:HGNC:46351]"}, {"versioned_ensembl_gene_id":"ENSG00000206682.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31505684,"end":31505788,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207392.1","gene_symbol":"SNORA20","gene_name":"small nucleolar RNA, H/ACA box 20 [Source:HGNC Symbol;Acc:HGNC:32610]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":159780250,"end":159780381,"strand":-1,"description":"small nucleolar RNA, H/ACA box 20 [Source:HGNC Symbol;Acc:HGNC:32610]"}, {"versioned_ensembl_gene_id":"ENSG00000200024.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87743952,"end":87744053,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207178.1","gene_symbol":"RNU6-1122P","gene_name":"RNA, U6 small nuclear 1122, pseudogene [Source:HGNC Symbol;Acc:HGNC:48085]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481936","summary":null,"start":182873841,"end":182873947,"strand":1,"description":"RNA, U6 small nuclear 1122, pseudogene [Source:HGNC Symbol;Acc:HGNC:48085]"}, {"versioned_ensembl_gene_id":"ENSG00000238405.1","gene_symbol":"RNA5SP311","gene_name":"RNA, 5S ribosomal pseudogene 311 [Source:HGNC Symbol;Acc:HGNC:43211]","synonyms":"RN5S314,RN5S311,RNA5SP314","biotype":"rRNA","ncbi_id":"106480358","summary":null,"start":46807458,"end":46807573,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 311 [Source:HGNC Symbol;Acc:HGNC:43211]"}, {"versioned_ensembl_gene_id":"ENSG00000207036.1","gene_symbol":"RNY3P14","gene_name":"RNA, Ro-associated Y3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50893]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480316","summary":null,"start":70357347,"end":70357448,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:50893]"}, {"versioned_ensembl_gene_id":"ENSG00000264931.1","gene_symbol":"MIR3138","gene_name":"microRNA 3138 [Source:HGNC Symbol;Acc:HGNC:38341]","synonyms":"hsa-mir-3138","biotype":"miRNA","ncbi_id":"100423011","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10078611,"end":10078692,"strand":-1,"description":"microRNA 3138 [Source:HGNC Symbol;Acc:HGNC:38341]"}, {"versioned_ensembl_gene_id":"ENSG00000221227.1","gene_symbol":"MIR1305","gene_name":"microRNA 1305 [Source:HGNC Symbol;Acc:HGNC:35303]","synonyms":"MIRN1305,hsa-mir-1305","biotype":"miRNA","ncbi_id":"100302270","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":182169293,"end":182169378,"strand":1,"description":"microRNA 1305 [Source:HGNC Symbol;Acc:HGNC:35303]"}, {"versioned_ensembl_gene_id":"ENSG00000264171.1","gene_symbol":"MIR4305","gene_name":"microRNA 4305 [Source:HGNC Symbol;Acc:HGNC:38301]","synonyms":"hsa-mir-4305","biotype":"miRNA","ncbi_id":"100422940","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39664034,"end":39664135,"strand":-1,"description":"microRNA 4305 [Source:HGNC Symbol;Acc:HGNC:38301]"}, {"versioned_ensembl_gene_id":"ENSG00000277031.1","gene_symbol":"RN7SL796P","gene_name":"RNA, 7SL, cytoplasmic 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:46812]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080653","summary":null,"start":30560644,"end":30560934,"strand":1,"description":"RNA, 7SL, cytoplasmic 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:46812]"}, {"versioned_ensembl_gene_id":"ENSG00000243424.2","gene_symbol":"RN7SL107P","gene_name":"RNA, 7SL, cytoplasmic 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:46123]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479262","summary":null,"start":80613544,"end":80613826,"strand":-1,"description":"RNA, 7SL, cytoplasmic 107, pseudogene [Source:HGNC Symbol;Acc:HGNC:46123]"}, {"versioned_ensembl_gene_id":"ENSG00000239823.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64390158,"end":64390263,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263838.1","gene_symbol":"MIR4698","gene_name":"microRNA 4698 [Source:HGNC Symbol;Acc:HGNC:41867]","synonyms":"hsa-mir-4698","biotype":"miRNA","ncbi_id":"100616486","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47187812,"end":47187891,"strand":1,"description":"microRNA 4698 [Source:HGNC Symbol;Acc:HGNC:41867]"}, {"versioned_ensembl_gene_id":"ENSG00000262710.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":153802951,"end":153803052,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238426.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41316488,"end":41316589,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222592.1","gene_symbol":"RNU6-887P","gene_name":"RNA, U6 small nuclear 887, pseudogene [Source:HGNC Symbol;Acc:HGNC:47850]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481459","summary":null,"start":39399149,"end":39399248,"strand":1,"description":"RNA, U6 small nuclear 887, pseudogene [Source:HGNC Symbol;Acc:HGNC:47850]"}, {"versioned_ensembl_gene_id":"ENSG00000222666.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":28408039,"end":28408251,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000201708.1","gene_symbol":"RNA5SP359","gene_name":"RNA, 5S ribosomal pseudogene 359 [Source:HGNC Symbol;Acc:HGNC:43259]","synonyms":"RN5S359","biotype":"rRNA","ncbi_id":"100873618","summary":null,"start":38163403,"end":38163515,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 359 [Source:HGNC Symbol;Acc:HGNC:43259]"}, {"versioned_ensembl_gene_id":"ENSG00000253038.1","gene_symbol":"RNU6-706P","gene_name":"RNA, U6 small nuclear 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:47669]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479878","summary":null,"start":39034007,"end":39034110,"strand":1,"description":"RNA, U6 small nuclear 706, pseudogene [Source:HGNC Symbol;Acc:HGNC:47669]"}, {"versioned_ensembl_gene_id":"ENSG00000202526.1","gene_symbol":"RNA5S13","gene_name":"RNA, 5S ribosomal 13 [Source:HGNC Symbol;Acc:HGNC:34374]","synonyms":"RN5S13","biotype":"rRNA","ncbi_id":"100169764","summary":null,"start":228637096,"end":228637214,"strand":-1,"description":"RNA, 5S ribosomal 13 [Source:HGNC Symbol;Acc:HGNC:34374]"}, {"versioned_ensembl_gene_id":"ENSG00000202205.1","gene_symbol":"RNU6-1034P","gene_name":"RNA, U6 small nuclear 1034, pseudogene [Source:HGNC Symbol;Acc:HGNC:47997]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480632","summary":null,"start":29445300,"end":29445400,"strand":-1,"description":"RNA, U6 small nuclear 1034, pseudogene [Source:HGNC Symbol;Acc:HGNC:47997]"}, {"versioned_ensembl_gene_id":"ENSG00000283836.1","gene_symbol":"MIR6734","gene_name":"microRNA 6734 [Source:HGNC Symbol;Acc:HGNC:50219]","synonyms":"hsa-mir-6734","biotype":"miRNA","ncbi_id":"102466723","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43364648,"end":43364715,"strand":-1,"description":"microRNA 6734 [Source:HGNC Symbol;Acc:HGNC:50219]"}, {"versioned_ensembl_gene_id":"ENSG00000222431.1","gene_symbol":"RNU6-141P","gene_name":"RNA, U6 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:47104]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480555","summary":null,"start":20452369,"end":20452473,"strand":-1,"description":"RNA, U6 small nuclear 141, pseudogene [Source:HGNC Symbol;Acc:HGNC:47104]"}, {"versioned_ensembl_gene_id":"ENSG00000206732.1","gene_symbol":"RNU6-936P","gene_name":"RNA, U6 small nuclear 936, pseudogene [Source:HGNC Symbol;Acc:HGNC:47899]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481924","summary":null,"start":24676309,"end":24676415,"strand":1,"description":"RNA, U6 small nuclear 936, pseudogene [Source:HGNC Symbol;Acc:HGNC:47899]"}, {"versioned_ensembl_gene_id":"ENSG00000264540.2","gene_symbol":"RN7SL405P","gene_name":"RNA, 7SL, cytoplasmic 405, pseudogene [Source:HGNC Symbol;Acc:HGNC:46421]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479373","summary":null,"start":44883986,"end":44884274,"strand":1,"description":"RNA, 7SL, cytoplasmic 405, pseudogene [Source:HGNC Symbol;Acc:HGNC:46421]"}, {"versioned_ensembl_gene_id":"ENSG00000238551.1","gene_symbol":"RNU6-1193P","gene_name":"RNA, U6 small nuclear 1193, pseudogene [Source:HGNC Symbol;Acc:HGNC:48156]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481556","summary":null,"start":64380194,"end":64380300,"strand":1,"description":"RNA, U6 small nuclear 1193, pseudogene [Source:HGNC Symbol;Acc:HGNC:48156]"}, {"versioned_ensembl_gene_id":"ENSG00000252155.1","gene_symbol":"RNU6-941P","gene_name":"RNA, U6 small nuclear 941, pseudogene [Source:HGNC Symbol;Acc:HGNC:47904]","synonyms":null,"biotype":"snRNA","ncbi_id":"107063612","summary":null,"start":7378672,"end":7378779,"strand":1,"description":"RNA, U6 small nuclear 941, pseudogene [Source:HGNC Symbol;Acc:HGNC:47904]"}, {"versioned_ensembl_gene_id":"ENSG00000281459.1","gene_symbol":"PADI1","gene_name":"peptidyl arginine deiminase 1 [Source:HGNC Symbol;Acc:HGNC:18367]","synonyms":"PDI1,PDI,PAD1,HPAD10","biotype":"protein_coding","ncbi_id":"29943","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type I enzyme is involved in the late stages of epidermal differentiation, where it deiminates filaggrin and keratin K1, which maintains hydration of the stratum corneum, and hence the cutaneous barrier function. This enzyme may also play a role in hair follicle formation. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17205126,"end":17246005,"strand":1,"description":"peptidyl arginine deiminase 1 [Source:HGNC Symbol;Acc:HGNC:18367]"}, {"versioned_ensembl_gene_id":"ENSG00000261709.3","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"SNORA11A,U107","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":45214906,"end":45215033,"strand":-1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000274144.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"hPrp31,hPrp31,RP11,RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31,PRP31","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000199319.1","gene_symbol":"RN7SKP25","gene_name":"RNA, 7SK small nuclear pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:45749]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480364","summary":null,"start":142673597,"end":142673904,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:45749]"}, {"versioned_ensembl_gene_id":"ENSG00000252348.1","gene_symbol":"RNU6-1256P","gene_name":"RNA, U6 small nuclear 1256, pseudogene [Source:HGNC Symbol;Acc:HGNC:48219]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480114","summary":null,"start":101615826,"end":101615928,"strand":1,"description":"RNA, U6 small nuclear 1256, pseudogene [Source:HGNC Symbol;Acc:HGNC:48219]"}, {"versioned_ensembl_gene_id":"ENSG00000252153.1","gene_symbol":"MIR2278","gene_name":"microRNA 2278 [Source:HGNC Symbol;Acc:HGNC:37315]","synonyms":"hsa-mir-2278","biotype":"miRNA","ncbi_id":"100313780","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94809962,"end":94810057,"strand":1,"description":"microRNA 2278 [Source:HGNC Symbol;Acc:HGNC:37315]"}, {"versioned_ensembl_gene_id":"ENSG00000202175.1","gene_symbol":"RNA5SP128","gene_name":"RNA, 5S ribosomal pseudogene 128 [Source:HGNC Symbol;Acc:HGNC:43028]","synonyms":"RN5S128","biotype":"rRNA","ncbi_id":"100873398","summary":null,"start":33491983,"end":33492098,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 128 [Source:HGNC Symbol;Acc:HGNC:43028]"}, {"versioned_ensembl_gene_id":"ENSG00000239078.1","gene_symbol":"RNU7-55P","gene_name":"RNA, U7 small nuclear 55 pseudogene [Source:HGNC Symbol;Acc:HGNC:10239]","synonyms":"U7.55,RNU7P4,HSU7.36","biotype":"snRNA","ncbi_id":"6075","summary":null,"start":9072455,"end":9072516,"strand":-1,"description":"RNA, U7 small nuclear 55 pseudogene [Source:HGNC Symbol;Acc:HGNC:10239]"}, {"versioned_ensembl_gene_id":"ENSG00000244056.3","gene_symbol":"RN7SL417P","gene_name":"RNA, 7SL, cytoplasmic 417, pseudogene [Source:HGNC Symbol;Acc:HGNC:46433]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080636","summary":null,"start":84394072,"end":84394336,"strand":1,"description":"RNA, 7SL, cytoplasmic 417, pseudogene [Source:HGNC Symbol;Acc:HGNC:46433]"}, {"versioned_ensembl_gene_id":"ENSG00000199804.1","gene_symbol":"RNA5SP383","gene_name":"RNA, 5S ribosomal pseudogene 383 [Source:HGNC Symbol;Acc:HGNC:43283]","synonyms":"RN5S383","biotype":"rRNA","ncbi_id":"100873638","summary":null,"start":24158603,"end":24158722,"strand":1,"description":"RNA, 5S ribosomal pseudogene 383 [Source:HGNC Symbol;Acc:HGNC:43283]"}, {"versioned_ensembl_gene_id":"ENSG00000276895.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":390790,"end":391079,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276823.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48524480,"end":48524806,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000251993.1","gene_symbol":"RNA5SP227","gene_name":"RNA, 5S ribosomal pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:43127]","synonyms":"RN5S227","biotype":"rRNA","ncbi_id":"100873485","summary":null,"start":22298594,"end":22298706,"strand":1,"description":"RNA, 5S ribosomal pseudogene 227 [Source:HGNC Symbol;Acc:HGNC:43127]"}, {"versioned_ensembl_gene_id":"ENSG00000206616.1","gene_symbol":"RNU6-741P","gene_name":"RNA, U6 small nuclear 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:47704]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479894","summary":null,"start":23777437,"end":23777543,"strand":-1,"description":"RNA, U6 small nuclear 741, pseudogene [Source:HGNC Symbol;Acc:HGNC:47704]"}, {"versioned_ensembl_gene_id":"ENSG00000201042.1","gene_symbol":"SNORA38","gene_name":"Small nucleolar RNA SNORA38 [Source:RFAM;Acc:RF00428]","synonyms":"ACA38,ACA38","biotype":"snoRNA","ncbi_id":"677820","summary":null,"start":118888434,"end":118888564,"strand":-1,"description":"Small nucleolar RNA SNORA38 [Source:RFAM;Acc:RF00428]"}, {"versioned_ensembl_gene_id":"ENSG00000201813.1","gene_symbol":"RNU6-915P","gene_name":"RNA, U6 small nuclear 915, pseudogene [Source:HGNC Symbol;Acc:HGNC:47878]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481923","summary":null,"start":195670372,"end":195670474,"strand":-1,"description":"RNA, U6 small nuclear 915, pseudogene [Source:HGNC Symbol;Acc:HGNC:47878]"}, {"versioned_ensembl_gene_id":"ENSG00000222506.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":171439526,"end":171439627,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201028.1","gene_symbol":"RNU6-151P","gene_name":"RNA, U6 small nuclear 151, pseudogene [Source:HGNC Symbol;Acc:HGNC:47114]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479633","summary":null,"start":111650431,"end":111650537,"strand":-1,"description":"RNA, U6 small nuclear 151, pseudogene [Source:HGNC Symbol;Acc:HGNC:47114]"}, {"versioned_ensembl_gene_id":"ENSG00000238842.1","gene_symbol":"RNU7-106P","gene_name":"RNA, U7 small nuclear 106 pseudogene [Source:HGNC Symbol;Acc:HGNC:45640]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479066","summary":null,"start":80068691,"end":80068757,"strand":-1,"description":"RNA, U7 small nuclear 106 pseudogene [Source:HGNC Symbol;Acc:HGNC:45640]"}, {"versioned_ensembl_gene_id":"ENSG00000200888.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45071442,"end":45071543,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212404.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":182828124,"end":182828221,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207367.1","gene_symbol":"RNU6-29P","gene_name":"RNA, U6 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:34273]","synonyms":"RNU6-29","biotype":"snRNA","ncbi_id":"107131122","summary":null,"start":48776965,"end":48777071,"strand":-1,"description":"RNA, U6 small nuclear 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:34273]"}, {"versioned_ensembl_gene_id":"ENSG00000207769.1","gene_symbol":"MIR586","gene_name":"microRNA 586 [Source:HGNC Symbol;Acc:HGNC:32842]","synonyms":"MIRN586,hsa-mir-586","biotype":"miRNA","ncbi_id":"693171","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45197674,"end":45197770,"strand":-1,"description":"microRNA 586 [Source:HGNC Symbol;Acc:HGNC:32842]"}, {"versioned_ensembl_gene_id":"ENSG00000211942.3","gene_symbol":"IGHV3-13","gene_name":"immunoglobulin heavy variable 3-13 [Source:HGNC Symbol;Acc:HGNC:5581]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28449","summary":null,"start":106129540,"end":106130072,"strand":-1,"description":"immunoglobulin heavy variable 3-13 [Source:HGNC Symbol;Acc:HGNC:5581]"}, {"versioned_ensembl_gene_id":"ENSG00000255326.1","gene_symbol":"AP001922.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75583196,"end":75594665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258380.1","gene_symbol":"AL356805.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89399995,"end":89409469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253534.1","gene_symbol":"TRBV6-8","gene_name":"T-cell receptor beta variable 6-8 [Source:HGNC Symbol;Acc:HGNC:12233]","synonyms":"TRBV68,TCRBV6S8,TCRBV13S7P","biotype":"TR_V_gene","ncbi_id":"28599","summary":null,"start":142507382,"end":142507810,"strand":1,"description":"T-cell receptor beta variable 6-8 [Source:HGNC Symbol;Acc:HGNC:12233]"}, {"versioned_ensembl_gene_id":"ENSG00000208023.3","gene_symbol":"MIR185","gene_name":"microRNA 185 [Source:HGNC Symbol;Acc:HGNC:31556]","synonyms":"MIRN185,hsa-mir-185","biotype":"miRNA","ncbi_id":"406961","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20033139,"end":20033220,"strand":1,"description":"microRNA 185 [Source:HGNC Symbol;Acc:HGNC:31556]"}, {"versioned_ensembl_gene_id":"ENSG00000276221.1","gene_symbol":"MIR8057","gene_name":"microRNA 8057 [Source:HGNC Symbol;Acc:HGNC:49960]","synonyms":"hsa-mir-8057","biotype":"miRNA","ncbi_id":"102466874","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26591467,"end":26591535,"strand":-1,"description":"microRNA 8057 [Source:HGNC Symbol;Acc:HGNC:49960]"}, {"versioned_ensembl_gene_id":"ENSG00000199903.1","gene_symbol":"RNU6-1273P","gene_name":"RNA, U6 small nuclear 1273, pseudogene [Source:HGNC Symbol;Acc:HGNC:48236]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481947","summary":null,"start":51037499,"end":51037602,"strand":1,"description":"RNA, U6 small nuclear 1273, pseudogene [Source:HGNC Symbol;Acc:HGNC:48236]"}, {"versioned_ensembl_gene_id":"ENSG00000252367.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":5113993,"end":5114083,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265871.1","gene_symbol":"MIR3174","gene_name":"microRNA 3174 [Source:HGNC Symbol;Acc:HGNC:38264]","synonyms":"hsa-mir-3174","biotype":"miRNA","ncbi_id":"100422841","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90006755,"end":90006841,"strand":1,"description":"microRNA 3174 [Source:HGNC Symbol;Acc:HGNC:38264]"}, {"versioned_ensembl_gene_id":"ENSG00000201436.1","gene_symbol":"RNU6-660P","gene_name":"RNA, U6 small nuclear 660, pseudogene [Source:HGNC Symbol;Acc:HGNC:47623]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480599","summary":null,"start":16941843,"end":16941951,"strand":-1,"description":"RNA, U6 small nuclear 660, pseudogene [Source:HGNC Symbol;Acc:HGNC:47623]"}, {"versioned_ensembl_gene_id":"ENSG00000201542.1","gene_symbol":"SNORA62","gene_name":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]","synonyms":"E2,RNE2,E2-1,RNU108","biotype":"snoRNA","ncbi_id":"6044","summary":null,"start":35310274,"end":35310425,"strand":1,"description":"Small nucleolar RNA SNORA62/SNORA6 family [Source:RFAM;Acc:RF00091]"}, {"versioned_ensembl_gene_id":"ENSG00000207020.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":139554900,"end":139555001,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252371.1","gene_symbol":"RNU6-725P","gene_name":"RNA, U6 small nuclear 725, pseudogene [Source:HGNC Symbol;Acc:HGNC:47688]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481408","summary":null,"start":238325687,"end":238325788,"strand":-1,"description":"RNA, U6 small nuclear 725, pseudogene [Source:HGNC Symbol;Acc:HGNC:47688]"}, {"versioned_ensembl_gene_id":"ENSG00000276137.1","gene_symbol":"MIR6133","gene_name":"microRNA 6133 [Source:HGNC Symbol;Acc:HGNC:50007]","synonyms":"hsa-mir-6133","biotype":"miRNA","ncbi_id":"102465139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133290881,"end":133290988,"strand":1,"description":"microRNA 6133 [Source:HGNC Symbol;Acc:HGNC:50007]"}, {"versioned_ensembl_gene_id":"ENSG00000201907.1","gene_symbol":"SNORD115-38","gene_name":"small nucleolar RNA, C/D box 115-38 [Source:HGNC Symbol;Acc:HGNC:33057]","synonyms":"HBII-52-38","biotype":"snoRNA","ncbi_id":"100033812","summary":null,"start":25239838,"end":25239919,"strand":1,"description":"small nucleolar RNA, C/D box 115-38 [Source:HGNC Symbol;Acc:HGNC:33057]"}, {"versioned_ensembl_gene_id":"ENSG00000276712.1","gene_symbol":"MIR7111","gene_name":"microRNA 7111 [Source:HGNC Symbol;Acc:HGNC:50073]","synonyms":"hsa-mir-7111","biotype":"miRNA","ncbi_id":"102465668","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35470508,"end":35470579,"strand":1,"description":"microRNA 7111 [Source:HGNC Symbol;Acc:HGNC:50073]"}, {"versioned_ensembl_gene_id":"ENSG00000086598.10","gene_symbol":"TMED2","gene_name":"transmembrane p24 trafficking protein 2 [Source:HGNC Symbol;Acc:HGNC:16996]","synonyms":"RNP24,p24beta1,p24b1,P24A","biotype":"protein_coding","ncbi_id":"10959","summary":null,"start":123584531,"end":123598577,"strand":1,"description":"transmembrane p24 trafficking protein 2 [Source:HGNC Symbol;Acc:HGNC:16996]"}, {"versioned_ensembl_gene_id":"ENSG00000224295.2","gene_symbol":"OLFM5P","gene_name":"olfactomedin family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:51927]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927763","summary":null,"start":5518441,"end":5524955,"strand":-1,"description":"olfactomedin family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:51927]"}, {"versioned_ensembl_gene_id":"ENSG00000277723.1","gene_symbol":"MIR6827","gene_name":"microRNA 6827 [Source:HGNC Symbol;Acc:HGNC:50234]","synonyms":"hsa-mir-6827","biotype":"miRNA","ncbi_id":"102466744","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134367804,"end":134367862,"strand":-1,"description":"microRNA 6827 [Source:HGNC Symbol;Acc:HGNC:50234]"}, {"versioned_ensembl_gene_id":"ENSG00000276359.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":164703026,"end":164703309,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283452.1","gene_symbol":"Clostridiales-1","gene_name":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]","synonyms":null,"biotype":"sRNA","ncbi_id":null,"summary":null,"start":75086368,"end":75086514,"strand":1,"description":"Clostridiales-1 RNA [Source:RFAM;Acc:RF01699]"}, {"versioned_ensembl_gene_id":"ENSG00000202490.1","gene_symbol":"RNU6-597P","gene_name":"RNA, U6 small nuclear 597, pseudogene [Source:HGNC Symbol;Acc:HGNC:47560]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481905","summary":null,"start":63618043,"end":63618144,"strand":1,"description":"RNA, U6 small nuclear 597, pseudogene [Source:HGNC Symbol;Acc:HGNC:47560]"}, {"versioned_ensembl_gene_id":"ENSG00000241391.3","gene_symbol":"RN7SL234P","gene_name":"RNA, 7SL, cytoplasmic 234, pseudogene [Source:HGNC Symbol;Acc:HGNC:46250]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479307","summary":null,"start":149291352,"end":149291646,"strand":1,"description":"RNA, 7SL, cytoplasmic 234, pseudogene [Source:HGNC Symbol;Acc:HGNC:46250]"}, {"versioned_ensembl_gene_id":"ENSG00000223126.1","gene_symbol":"RN7SKP263","gene_name":"RNA, 7SK small nuclear pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:45987]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480913","summary":null,"start":94008739,"end":94009047,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 263 [Source:HGNC Symbol;Acc:HGNC:45987]"}, {"versioned_ensembl_gene_id":"ENSG00000200176.1","gene_symbol":"RNU1-19P","gene_name":"RNA, U1 small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:41945]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873861","summary":null,"start":86889569,"end":86889733,"strand":1,"description":"RNA, U1 small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:41945]"}, {"versioned_ensembl_gene_id":"ENSG00000222969.1","gene_symbol":"RN7SKP8","gene_name":"RNA, 7SK small nuclear pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42626]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873852","summary":null,"start":98203835,"end":98204192,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42626]"}, {"versioned_ensembl_gene_id":"ENSG00000207384.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":139200395,"end":139200513,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199767.1","gene_symbol":"RNU6-78P","gene_name":"RNA, U6 small nuclear 78, pseudogene [Source:HGNC Symbol;Acc:HGNC:42568]","synonyms":"RNU6-78","biotype":"snRNA","ncbi_id":"100873778","summary":null,"start":25517119,"end":25517225,"strand":1,"description":"RNA, U6 small nuclear 78, pseudogene [Source:HGNC Symbol;Acc:HGNC:42568]"}, {"versioned_ensembl_gene_id":"ENSG00000207266.1","gene_symbol":"RNU6-1241P","gene_name":"RNA, U6 small nuclear 1241, pseudogene [Source:HGNC Symbol;Acc:HGNC:48204]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481572","summary":null,"start":27998295,"end":27998401,"strand":-1,"description":"RNA, U6 small nuclear 1241, pseudogene [Source:HGNC Symbol;Acc:HGNC:48204]"}, {"versioned_ensembl_gene_id":"ENSG00000244044.3","gene_symbol":"RN7SL735P","gene_name":"RNA, 7SL, cytoplasmic 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:46751]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480529","summary":null,"start":66364029,"end":66364320,"strand":1,"description":"RNA, 7SL, cytoplasmic 735, pseudogene [Source:HGNC Symbol;Acc:HGNC:46751]"}, {"versioned_ensembl_gene_id":"ENSG00000252349.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":19662000,"end":19662090,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000108679.12","gene_symbol":"LGALS3BP","gene_name":"galectin 3 binding protein [Source:HGNC Symbol;Acc:HGNC:6564]","synonyms":"TANGO10B,MAC-2-BP,M2BP,gp90,CyCAP,BTBD17B,90K","biotype":"protein_coding","ncbi_id":"3959","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. LGALS3BP has been found elevated in the serum of patients with cancer and in those infected by the human immunodeficiency virus (HIV). It appears to be implicated in immune response associated with natural killer (NK) and lymphokine-activated killer (LAK) cell cytotoxicity. Using fluorescence in situ hybridization the full length 90K cDNA has been localized to chromosome 17q25. The native protein binds specifically to a human macrophage-associated lectin known as Mac-2 and also binds galectin 1. [provided by RefSeq, Jul 2008]","start":78971238,"end":78980109,"strand":-1,"description":"galectin 3 binding protein [Source:HGNC Symbol;Acc:HGNC:6564]"}, {"versioned_ensembl_gene_id":"ENSG00000275329.1","gene_symbol":"AL138781.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136122521,"end":136124363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178199.13","gene_symbol":"ZC3H12D","gene_name":"zinc finger CCCH-type containing 12D [Source:HGNC Symbol;Acc:HGNC:21175]","synonyms":"MCPIP4,dJ281H8.1,C6orf95","biotype":"protein_coding","ncbi_id":"340152","summary":null,"start":149446795,"end":149485061,"strand":-1,"description":"zinc finger CCCH-type containing 12D [Source:HGNC Symbol;Acc:HGNC:21175]"}, {"versioned_ensembl_gene_id":"ENSG00000108849.7","gene_symbol":"PPY","gene_name":"pancreatic polypeptide [Source:HGNC Symbol;Acc:HGNC:9327]","synonyms":"PNP","biotype":"protein_coding","ncbi_id":"5539","summary":"This gene encodes a member of the neuropeptide Y (NPY) family of peptides. The encoded 95 aa preproprotein is synthesized in the pancreatic islets of Langerhans and proteolytically processed to generate two peptide products. These products include the active pancreatic hormone of 36 aa and an icosapeptide of unknown function. This hormone acts as a regulator of pancreatic and gastrointestinal functions and may be important in the regulation of food intake. Plasma level of this hormone has been shown to be reduced in conditions associated with increased food intake and elevated in anorexia nervosa. In addition, infusion of this hormone in obese rodents has shown to decrease weight gain. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":43940804,"end":43942468,"strand":-1,"description":"pancreatic polypeptide [Source:HGNC Symbol;Acc:HGNC:9327]"}, {"versioned_ensembl_gene_id":"ENSG00000267420.1","gene_symbol":"AC007993.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43927563,"end":43932622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259230.1","gene_symbol":"LINC02323","gene_name":"long intergenic non-protein coding RNA 2323 [Source:HGNC Symbol;Acc:HGNC:53242]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370681","summary":null,"start":102545254,"end":102555826,"strand":1,"description":"long intergenic non-protein coding RNA 2323 [Source:HGNC Symbol;Acc:HGNC:53242]"}, {"versioned_ensembl_gene_id":"ENSG00000113583.7","gene_symbol":"C5orf15","gene_name":"chromosome 5 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:20656]","synonyms":"KCT2,HTGN29","biotype":"protein_coding","ncbi_id":"56951","summary":null,"start":133955502,"end":133968787,"strand":-1,"description":"chromosome 5 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:20656]"}, {"versioned_ensembl_gene_id":"ENSG00000276742.1","gene_symbol":"AL731566.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121956782,"end":121957098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249941.1","gene_symbol":"AC026415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4866521,"end":4874759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100739.10","gene_symbol":"BDKRB1","gene_name":"bradykinin receptor B1 [Source:HGNC Symbol;Acc:HGNC:1029]","synonyms":"bradyb1,BKR1,B1BKR","biotype":"protein_coding","ncbi_id":"623","summary":"Bradykinin, a 9 aa peptide, is generated in pathophysiologic conditions such as inflammation, trauma, burns, shock, and allergy. The protein encoded by this gene belongs to the G-protein coupled receptor 1 family. Two types of G-protein coupled receptors have been found which bind bradykinin and mediate responses to these pathophysiologic conditions. The protein encoded by this gene is one of these receptors and is synthesized de novo following tissue injury. Receptor binding leads to an increase in the cytosolic calcium ion concentration, ultimately resulting in chronic and acute inflammatory responses. [provided by RefSeq, Aug 2020]","start":96255824,"end":96268967,"strand":1,"description":"bradykinin receptor B1 [Source:HGNC Symbol;Acc:HGNC:1029]"}, {"versioned_ensembl_gene_id":"ENSG00000258691.1","gene_symbol":"AL355102.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":96204844,"end":96263929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165672.6","gene_symbol":"PRDX3","gene_name":"peroxiredoxin 3 [Source:HGNC Symbol;Acc:HGNC:9354]","synonyms":"SP-22,MER5,AOP1,AOP-1","biotype":"protein_coding","ncbi_id":"10935","summary":"This gene encodes a mitochondrial protein with antioxidant function. The protein is similar to the C22 subunit of Salmonella typhimurium alkylhydroperoxide reductase, and it can rescue bacterial resistance to alkylhydroperoxide in E. coli that lack the C22 subunit. The human and mouse genes are highly conserved, and they map to the regions syntenic between mouse and human chromosomes. Sequence comparisons with recently cloned mammalian homologs suggest that these genes consist of a family that is responsible for the regulation of cellular proliferation, differentiation and antioxidant functions. This family member can protect cells from oxidative stress, and it can promote cell survival in prostate cancer. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 3, 13 and 22. [provided by RefSeq, Oct 2014]","start":119167703,"end":119178833,"strand":-1,"description":"peroxiredoxin 3 [Source:HGNC Symbol;Acc:HGNC:9354]"}, {"versioned_ensembl_gene_id":"ENSG00000198570.5","gene_symbol":"RD3","gene_name":"retinal degeneration 3 [Source:HGNC Symbol;Acc:HGNC:19689]","synonyms":"LCA12,C1orf36","biotype":"protein_coding","ncbi_id":"343035","summary":"This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":211476522,"end":211492917,"strand":-1,"description":"retinal degeneration 3 [Source:HGNC Symbol;Acc:HGNC:19689]"}, {"versioned_ensembl_gene_id":"ENSG00000230246.7","gene_symbol":"SPATA31C1","gene_name":"SPATA31 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:27846]","synonyms":"FLJ36055,FAM75C1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441452","summary":null,"start":87914493,"end":87923505,"strand":1,"description":"SPATA31 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:27846]"}, {"versioned_ensembl_gene_id":"ENSG00000223774.5","gene_symbol":"AL513217.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201893842,"end":201899978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233884.1","gene_symbol":"AL772337.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87848113,"end":87853442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226453.1","gene_symbol":"LINC02542","gene_name":"long intergenic non-protein coding RNA 2542 [Source:HGNC Symbol;Acc:HGNC:53576]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724168","summary":null,"start":81845185,"end":81933480,"strand":-1,"description":"long intergenic non-protein coding RNA 2542 [Source:HGNC Symbol;Acc:HGNC:53576]"}, {"versioned_ensembl_gene_id":"ENSG00000249808.2","gene_symbol":"LINC01377","gene_name":"long intergenic non-protein coding RNA 1377 [Source:NCBI gene;Acc:102467074]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467074","summary":null,"start":3177835,"end":3181232,"strand":1,"description":"long intergenic non-protein coding RNA 1377 [Source:NCBI gene;Acc:102467074]"}, {"versioned_ensembl_gene_id":"ENSG00000248550.3","gene_symbol":"OTX2-AS1","gene_name":"OTX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43906]","synonyms":"OTX2OS1","biotype":"lincRNA","ncbi_id":"100309464","summary":null,"start":56813183,"end":57152177,"strand":1,"description":"OTX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43906]"}, {"versioned_ensembl_gene_id":"ENSG00000233262.1","gene_symbol":"AL356134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84278219,"end":84290131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268234.1","gene_symbol":"FKBP4P6","gene_name":"FK506 binding protein 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50375]","synonyms":"FKBP4P5,FKBP4P4","biotype":"processed_pseudogene","ncbi_id":"100132268","summary":null,"start":42384805,"end":42386136,"strand":1,"description":"FK506 binding protein 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50375]"}, {"versioned_ensembl_gene_id":"ENSG00000173598.13","gene_symbol":"NUDT4","gene_name":"nudix hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:8051]","synonyms":"KIAA0487,HDCMB47P,DIPP2beta,DIPP2alpha,DIPP2","biotype":"protein_coding","ncbi_id":"11163","summary":"The protein encoded by this gene regulates the turnover of diphosphoinositol polyphosphates. The turnover of these high-energy diphosphoinositol polyphosphates represents a molecular switching activity with important regulatory consequences. Molecular switching by diphosphoinositol polyphosphates may contribute to regulating intracellular trafficking. Several alternatively spliced transcript variants have been described, but the full-length nature of some variants has not been determined. Isoforms DIPP2alpha and DIPP2beta are distinguishable from each other solely by DIPP2beta possessing one additional amino acid due to intron boundary skidding in alternate splicing. [provided by RefSeq, Jul 2008]","start":93377883,"end":93408146,"strand":1,"description":"nudix hydrolase 4 [Source:HGNC Symbol;Acc:HGNC:8051]"}, {"versioned_ensembl_gene_id":"ENSG00000259163.1","gene_symbol":"AL096869.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90642638,"end":90648894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135476.11","gene_symbol":"ESPL1","gene_name":"extra spindle pole bodies like 1, separase [Source:HGNC Symbol;Acc:HGNC:16856]","synonyms":"SEPA,KIAA0165,ESP1","biotype":"protein_coding","ncbi_id":"9700","summary":"Stable cohesion between sister chromatids before anaphase and their timely separation during anaphase are critical for chromosome inheritance. In vertebrates, sister chromatid cohesion is released in 2 steps via distinct mechanisms. The first step involves phosphorylation of STAG1 (MIM 604358) or STAG2 (MIM 300826) in the cohesin complex. The second step involves cleavage of the cohesin subunit SCC1 (RAD21; MIM 606462) by ESPL1, or separase, which initiates the final separation of sister chromatids (Sun et al., 2009 [PubMed 19345191]).[supplied by OMIM, Nov 2010]","start":53268299,"end":53293643,"strand":1,"description":"extra spindle pole bodies like 1, separase [Source:HGNC Symbol;Acc:HGNC:16856]"}, {"versioned_ensembl_gene_id":"ENSG00000161036.12","gene_symbol":"LRWD1","gene_name":"leucine rich repeats and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21769]","synonyms":"ORCA,DKFZp434K1815,CENP-33","biotype":"protein_coding","ncbi_id":"222229","summary":"The protein encoded by this gene interacts with components of the origin recognition complex (ORC) and regulates the formation of the prereplicative complex. The encoded protein stabilizes the ORC and therefore aids in DNA replication. This protein is required for the G1/S phase transition of the cell cycle. In addition, the encoded protein binds to trimethylated histone H3 in heterochromatin and recruits the ORC and lysine methyltransferases, which help maintain the repressive heterochromatic state. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":102464929,"end":102473168,"strand":1,"description":"leucine rich repeats and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21769]"}, {"versioned_ensembl_gene_id":"ENSG00000224658.1","gene_symbol":"AL513164.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148237585,"end":148283408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155511.17","gene_symbol":"GRIA1","gene_name":"glutamate ionotropic receptor AMPA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4571]","synonyms":"GLURA,GLUR1,GluA1","biotype":"protein_coding","ncbi_id":"2890","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes with multiple subunits, each possessing transmembrane regions, and all arranged to form a ligand-gated ion channel. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. This gene belongs to a family of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":153489615,"end":153813869,"strand":1,"description":"glutamate ionotropic receptor AMPA type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4571]"}, {"versioned_ensembl_gene_id":"ENSG00000135913.10","gene_symbol":"USP37","gene_name":"ubiquitin specific peptidase 37 [Source:HGNC Symbol;Acc:HGNC:20063]","synonyms":"KIAA1594","biotype":"protein_coding","ncbi_id":"57695","summary":null,"start":218450251,"end":218568361,"strand":-1,"description":"ubiquitin specific peptidase 37 [Source:HGNC Symbol;Acc:HGNC:20063]"}, {"versioned_ensembl_gene_id":"ENSG00000259036.1","gene_symbol":"AL355102.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96233431,"end":96234101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278949.1","gene_symbol":"AC127070.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132865855,"end":132867958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235105.1","gene_symbol":"AL356968.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48435967,"end":48437223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011332.19","gene_symbol":"DPF1","gene_name":"double PHD fingers 1 [Source:HGNC Symbol;Acc:HGNC:20225]","synonyms":"neuro-d4,NEUD4,BAF45b","biotype":"protein_coding","ncbi_id":"8193","summary":null,"start":38211006,"end":38229714,"strand":-1,"description":"double PHD fingers 1 [Source:HGNC Symbol;Acc:HGNC:20225]"}, {"versioned_ensembl_gene_id":"ENSG00000233873.1","gene_symbol":"RPL7P44","gene_name":"ribosomal protein L7 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36143]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390413","summary":null,"start":76981175,"end":76981916,"strand":-1,"description":"ribosomal protein L7 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36143]"}, {"versioned_ensembl_gene_id":"ENSG00000207955.5","gene_symbol":"MIR219A2","gene_name":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]","synonyms":"MIRN219-2,MIR219-2,hsa-mir-219-2,MIRN219-2,MIR219-2,hsa-mir-219-2","biotype":"lincRNA","ncbi_id":"407003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128392007,"end":128393510,"strand":-1,"description":"microRNA 219a-2 [Source:HGNC Symbol;Acc:HGNC:31598]"}, {"versioned_ensembl_gene_id":"ENSG00000135047.14","gene_symbol":"CTSL","gene_name":"cathepsin L [Source:HGNC Symbol;Acc:HGNC:2537]","synonyms":"CTSL1,FLJ31037","biotype":"protein_coding","ncbi_id":"1514","summary":"The protein encoded by this gene is a lysosomal cysteine proteinase that plays a major role in intracellular protein catabolism. Its substrates include collagen and elastin, as well as alpha-1 protease inhibitor, a major controlling element of neutrophil elastase activity. The encoded protein has been implicated in several pathologic processes, including myofibril necrosis in myopathies and in myocardial ischemia, and in the renal tubular response to proteinuria. This protein, which is a member of the peptidase C1 family, is a dimer composed of disulfide-linked heavy and light chains, both produced from a single protein precursor. Additionally, this protein cleaves the S1 subunit of the SARS-CoV-2 spike protein, which is necessary for entry of the virus into the cell. [provided by RefSeq, Aug 2020]","start":87725519,"end":87731393,"strand":1,"description":"cathepsin L [Source:HGNC Symbol;Acc:HGNC:2537]"}, {"versioned_ensembl_gene_id":"ENSG00000198668.10","gene_symbol":"CALM1","gene_name":"calmodulin 1 [Source:HGNC Symbol;Acc:HGNC:1442]","synonyms":"PHKD,DD132,CAMI,CALML2","biotype":"protein_coding","ncbi_id":"801","summary":"This gene encodes one of three calmodulin proteins which are members of the EF-hand calcium-binding protein family. Calcium-induced activation of calmodulin regulates and modulates the function of cardiac ion channels. Two pseudogenes have been identified on chromosome 7 and X. Multiple transcript variants encoding different isoforms have been found for this gene.A missense mutation in the CALM1 gene has been associated with ventricular tachycardia.[provided by RefSeq, May 2020]","start":90396502,"end":90408261,"strand":1,"description":"calmodulin 1 [Source:HGNC Symbol;Acc:HGNC:1442]"}, {"versioned_ensembl_gene_id":"ENSG00000262803.1","gene_symbol":"AL354943.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70693839,"end":70694619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258428.5","gene_symbol":"AL161757.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56633244,"end":56648658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260457.2","gene_symbol":"AC027458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71837039,"end":71870788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242995.1","gene_symbol":"AL161757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56683421,"end":56683741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275520.1","gene_symbol":"FAM236A","gene_name":"family with sequence similarity 235 member A [Source:HGNC Symbol;Acc:HGNC:44268]","synonyms":"DMRTC1-AS1,LINC00684","biotype":"protein_coding","ncbi_id":"100129407","summary":null,"start":72938163,"end":72938958,"strand":1,"description":"family with sequence similarity 235 member A [Source:HGNC Symbol;Acc:HGNC:44268]"}, {"versioned_ensembl_gene_id":"ENSG00000091527.15","gene_symbol":"CDV3","gene_name":"CDV3 homolog [Source:HGNC Symbol;Acc:HGNC:26928]","synonyms":"H41","biotype":"protein_coding","ncbi_id":"55573","summary":null,"start":133573730,"end":133590261,"strand":1,"description":"CDV3 homolog [Source:HGNC Symbol;Acc:HGNC:26928]"}, {"versioned_ensembl_gene_id":"ENSG00000265845.2","gene_symbol":"AC024267.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28926275,"end":28944749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263613.1","gene_symbol":"AC024619.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29009799,"end":29011009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232373.2","gene_symbol":"MTCYBP3","gene_name":"mitochondrially encoded cytochrome b pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39579]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873204","summary":null,"start":95694569,"end":95695705,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39579]"}, {"versioned_ensembl_gene_id":"ENSG00000257252.5","gene_symbol":"AC124947.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93317135,"end":93377736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161649.12","gene_symbol":"CD300LG","gene_name":"CD300 molecule like family member g [Source:HGNC Symbol;Acc:HGNC:30455]","synonyms":"Trem4,CLM9","biotype":"protein_coding","ncbi_id":"146894","summary":"Members of the CD300 (see MIM 606786)-like (CD300L) family, such as CD300LG, are widely expressed on hematopoietic cells. All CD300L proteins are type I cell surface glycoproteins that contain a single immunoglobulin (Ig) V-like domain (Takatsu et al., 2006 [PubMed 16876123]).[supplied by OMIM, Mar 2008]","start":43847148,"end":43863629,"strand":1,"description":"CD300 molecule like family member g [Source:HGNC Symbol;Acc:HGNC:30455]"}, {"versioned_ensembl_gene_id":"ENSG00000227714.1","gene_symbol":"MTND6P18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39481]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478951","summary":null,"start":95693983,"end":95694495,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39481]"}, {"versioned_ensembl_gene_id":"ENSG00000137501.17","gene_symbol":"SYTL2","gene_name":"synaptotagmin like 2 [Source:HGNC Symbol;Acc:HGNC:15585]","synonyms":"SLP2,SGA72M,PPP1R151,MGC102768,KIAA1597,FLJ21219,FLJ20163,exophilin-4,CHR11SYT","biotype":"protein_coding","ncbi_id":"54843","summary":"The protein encoded by this gene is a synaptotagmin-like protein (SLP) that belongs to a C2 domain-containing protein family. The SLP homology domain (SHD) of this protein has been shown to specifically bind the GTP-bound form of Ras-related protein Rab-27A (RAB27A). This protein plays a role in RAB27A-dependent vesicle trafficking and controls melanosome distribution in the cell periphery. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jun 2009]","start":85694224,"end":85811159,"strand":-1,"description":"synaptotagmin like 2 [Source:HGNC Symbol;Acc:HGNC:15585]"}, {"versioned_ensembl_gene_id":"ENSG00000237571.1","gene_symbol":"AC073284.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":215274992,"end":215277947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183479.12","gene_symbol":"TREX2","gene_name":"three prime repair exonuclease 2 [Source:HGNC Symbol;Acc:HGNC:12270]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11219","summary":"This gene encodes a nuclear protein with 3' to 5' exonuclease activity. The encoded protein participates in double-stranded DNA break repair, and may interact with DNA polymerase delta. [provided by RefSeq, Nov 2012]","start":153444720,"end":153470587,"strand":-1,"description":"three prime repair exonuclease 2 [Source:HGNC Symbol;Acc:HGNC:12270]"}, {"versioned_ensembl_gene_id":"ENSG00000255243.1","gene_symbol":"AC099687.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26189123,"end":26208347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268471.6","gene_symbol":"LINC02486","gene_name":"long intergenic non-protein coding RNA 2486 [Source:HGNC Symbol;Acc:HGNC:25288]","synonyms":"DKFZP434I0714","biotype":"lincRNA","ncbi_id":"54553","summary":null,"start":152536264,"end":152539263,"strand":1,"description":"long intergenic non-protein coding RNA 2486 [Source:HGNC Symbol;Acc:HGNC:25288]"}, {"versioned_ensembl_gene_id":"ENSG00000156171.14","gene_symbol":"DRAM2","gene_name":"DNA damage regulated autophagy modulator 2 [Source:HGNC Symbol;Acc:HGNC:28769]","synonyms":"WWFQ154,TMEM77,RP5-1180E21.1,PRO180,MGC54289","biotype":"protein_coding","ncbi_id":"128338","summary":"The protein encoded by this gene binds microtubule-associated protein 1 light chain 3 and is required for autophagy. Defects in this gene are a cause of retinal dystrophy. In addition, two microRNAs (microRNA 125b-1 and microRNA 144) can bind to the mRNA of this gene and produce the disease state. [provided by RefSeq, Mar 2017]","start":111117333,"end":111140216,"strand":-1,"description":"DNA damage regulated autophagy modulator 2 [Source:HGNC Symbol;Acc:HGNC:28769]"}, {"versioned_ensembl_gene_id":"ENSG00000267353.1","gene_symbol":"AC020928.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36773712,"end":36775908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229870.1","gene_symbol":"RPL21P89","gene_name":"ribosomal protein L21 pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:36474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271422","summary":null,"start":49815096,"end":49815562,"strand":1,"description":"ribosomal protein L21 pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:36474]"}, {"versioned_ensembl_gene_id":"ENSG00000245904.3","gene_symbol":"AC025164.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92145573,"end":92189660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197766.7","gene_symbol":"CFD","gene_name":"complement factor D [Source:HGNC Symbol;Acc:HGNC:2771]","synonyms":"ADN,PFD,DF","biotype":"protein_coding","ncbi_id":"1675","summary":"This gene encodes a member of the S1, or chymotrypsin, family of serine peptidases. This protease catalyzes the cleavage of factor B, the rate-limiting step of the alternative pathway of complement activation. This protein also functions as an adipokine, a cell signaling protein secreted by adipocytes, which regulates insulin secretion in mice. Mutations in this gene underlie complement factor D deficiency, which is associated with recurrent bacterial meningitis infections in human patients. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature protease. [provided by RefSeq, Nov 2015]","start":859643,"end":863630,"strand":1,"description":"complement factor D [Source:HGNC Symbol;Acc:HGNC:2771]"}, {"versioned_ensembl_gene_id":"ENSG00000273569.1","gene_symbol":"AC008432.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163855140,"end":163856642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225190.10","gene_symbol":"PLEKHM1","gene_name":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]","synonyms":"KIAA0356","biotype":"protein_coding","ncbi_id":"9842","summary":"The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":45435900,"end":45490749,"strand":-1,"description":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]"}, {"versioned_ensembl_gene_id":"ENSG00000181038.13","gene_symbol":"METTL23","gene_name":"methyltransferase like 23 [Source:HGNC Symbol;Acc:HGNC:26988]","synonyms":"LOC124512,C17orf95","biotype":"protein_coding","ncbi_id":"124512","summary":"The protein encoded by this gene functions as a transcription factor regulator in the transcriptional pathway for human cognition. It is a partner of the alpha subunit of the GA-binding protein transcription factor. Mutations in this gene cause mild autosomal recessive intellectual disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":76726830,"end":76733936,"strand":1,"description":"methyltransferase like 23 [Source:HGNC Symbol;Acc:HGNC:26988]"}, {"versioned_ensembl_gene_id":"ENSG00000243859.3","gene_symbol":"RPL5P17","gene_name":"ribosomal protein L5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36605]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270839","summary":null,"start":85464434,"end":85465310,"strand":1,"description":"ribosomal protein L5 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36605]"}, {"versioned_ensembl_gene_id":"ENSG00000257345.2","gene_symbol":"LINC02413","gene_name":"long intergenic non-protein coding RNA 2413 [Source:HGNC Symbol;Acc:HGNC:53342]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369906","summary":null,"start":92999218,"end":93019820,"strand":1,"description":"long intergenic non-protein coding RNA 2413 [Source:HGNC Symbol;Acc:HGNC:53342]"}, {"versioned_ensembl_gene_id":"ENSG00000248170.1","gene_symbol":"AC117522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85237681,"end":85238074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259483.1","gene_symbol":"AL355073.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56303490,"end":56310761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275569.1","gene_symbol":"AL355073.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56305838,"end":56306394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258122.1","gene_symbol":"AC044802.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66841433,"end":66853448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217514.1","gene_symbol":"AL031121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163363210,"end":163363463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143315.6","gene_symbol":"PIGM","gene_name":"phosphatidylinositol glycan anchor biosynthesis class M [Source:HGNC Symbol;Acc:HGNC:18858]","synonyms":"GPI-MT-I","biotype":"protein_coding","ncbi_id":"93183","summary":"This gene encodes a transmembrane protein that is located in the endoplasmic reticulum and is involved in GPI-anchor biosynthesis. The glycosylphosphatidylinositol (GPI)-anchor is a glycolipid which contains three mannose molecules in its core backbone. The GPI-anchor is found on many blood cells and serves to anchor proteins to the cell surface. This gene encodes a mannosyltransferase, GPI-MT-I, that transfers the first mannose to GPI on the lumenal side of the endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":160027673,"end":160031991,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class M [Source:HGNC Symbol;Acc:HGNC:18858]"}, {"versioned_ensembl_gene_id":"ENSG00000254949.1","gene_symbol":"AP001781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111864254,"end":111864460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275407.1","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"cl-43,CD158B1,nkat6,CD158k","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754722,"end":54769049,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000149547.14","gene_symbol":"EI24","gene_name":"EI24, autophagy associated transmembrane protein [Source:HGNC Symbol;Acc:HGNC:13276]","synonyms":"TP53I8,PIG8,EPG4","biotype":"protein_coding","ncbi_id":"9538","summary":"This gene encodes a putative tumor suppressor and has higher expression in p53-expressing cells than in control cells and is an immediate-early induction target of p53-mediated apoptosis. The encoded protein may suppress cell growth by inducing apoptotic cell death through the caspase 9 and mitochondrial pathways. This gene is located on human chromosome 11q24, a region frequently altered in cancers. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 1, 3, 7, and 8. [provided by RefSeq, Feb 2014]","start":125569216,"end":125584687,"strand":1,"description":"EI24, autophagy associated transmembrane protein [Source:HGNC Symbol;Acc:HGNC:13276]"}, {"versioned_ensembl_gene_id":"ENSG00000188958.9","gene_symbol":"UTS2B","gene_name":"urotensin 2B [Source:HGNC Symbol;Acc:HGNC:30894]","synonyms":"URP,U2B,UTS2D","biotype":"protein_coding","ncbi_id":"257313","summary":null,"start":191267168,"end":191330536,"strand":-1,"description":"urotensin 2B [Source:HGNC Symbol;Acc:HGNC:30894]"}, {"versioned_ensembl_gene_id":"ENSG00000182534.13","gene_symbol":"MXRA7","gene_name":"matrix remodeling associated 7 [Source:HGNC Symbol;Acc:HGNC:7541]","synonyms":"TMAP1,PS1TP1,FLJ46603","biotype":"protein_coding","ncbi_id":"439921","summary":null,"start":76672551,"end":76711016,"strand":-1,"description":"matrix remodeling associated 7 [Source:HGNC Symbol;Acc:HGNC:7541]"}, {"versioned_ensembl_gene_id":"ENSG00000267084.1","gene_symbol":"AC015802.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76595584,"end":76595772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160991.15","gene_symbol":"ORAI2","gene_name":"ORAI calcium release-activated calcium modulator 2 [Source:HGNC Symbol;Acc:HGNC:21667]","synonyms":"TMEM142B,H_NH0514P08.8,FLJ14733,FLJ12474,CBCIP2,C7orf19","biotype":"protein_coding","ncbi_id":"80228","summary":null,"start":102433106,"end":102456821,"strand":1,"description":"ORAI calcium release-activated calcium modulator 2 [Source:HGNC Symbol;Acc:HGNC:21667]"}, {"versioned_ensembl_gene_id":"ENSG00000273933.1","gene_symbol":"AL513485.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":159972548,"end":159974064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274339.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000000460.16","gene_symbol":"C1orf112","gene_name":"chromosome 1 open reading frame 112 [Source:HGNC Symbol;Acc:HGNC:25565]","synonyms":"FLJ10706","biotype":"protein_coding","ncbi_id":"55732","summary":null,"start":169662007,"end":169854080,"strand":1,"description":"chromosome 1 open reading frame 112 [Source:HGNC Symbol;Acc:HGNC:25565]"}, {"versioned_ensembl_gene_id":"ENSG00000139546.10","gene_symbol":"TARBP2","gene_name":"TARBP2, RISC loading complex RNA binding subunit [Source:HGNC Symbol;Acc:HGNC:11569]","synonyms":"Trbp","biotype":"protein_coding","ncbi_id":"6895","summary":"HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expression by the transactivator Tat is dependent on an RNA regulatory element (TAR) located downstream of the transcription initiation site. The protein encoded by this gene binds between the bulge and the loop of the HIV-1 TAR RNA regulatory element and activates HIV-1 gene expression in synergy with the viral Tat protein. Alternative splicing results in multiple transcript variants encoding different isoforms. This gene also has a pseudogene. [provided by RefSeq, Jul 2008]","start":53500921,"end":53506431,"strand":1,"description":"TARBP2, RISC loading complex RNA binding subunit [Source:HGNC Symbol;Acc:HGNC:11569]"}, {"versioned_ensembl_gene_id":"ENSG00000196826.7","gene_symbol":"AC008758.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12461559,"end":12551474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196466.10","gene_symbol":"ZNF799","gene_name":"zinc finger protein 799 [Source:HGNC Symbol;Acc:HGNC:28071]","synonyms":"ZNF842,MGC71805,HIT-40","biotype":"protein_coding","ncbi_id":"90576","summary":null,"start":12390016,"end":12401271,"strand":-1,"description":"zinc finger protein 799 [Source:HGNC Symbol;Acc:HGNC:28071]"}, {"versioned_ensembl_gene_id":"ENSG00000168916.15","gene_symbol":"ZNF608","gene_name":"zinc finger protein 608 [Source:HGNC Symbol;Acc:HGNC:29238]","synonyms":"NY-REN-36,KIAA1281,DKFZp434M098","biotype":"protein_coding","ncbi_id":"57507","summary":null,"start":124636913,"end":124748807,"strand":-1,"description":"zinc finger protein 608 [Source:HGNC Symbol;Acc:HGNC:29238]"}, {"versioned_ensembl_gene_id":"ENSG00000232610.1","gene_symbol":"CCT6P4","gene_name":"chaperonin containing TCP1 subunit 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35148]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130481","summary":null,"start":190714811,"end":190716399,"strand":1,"description":"chaperonin containing TCP1 subunit 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35148]"}, {"versioned_ensembl_gene_id":"ENSG00000152939.14","gene_symbol":"MARVELD2","gene_name":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]","synonyms":"TRIC,MRVLDC2,FLJ30532,DFNB49","biotype":"protein_coding","ncbi_id":"153562","summary":"The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":69415112,"end":69444330,"strand":1,"description":"MARVEL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26401]"}, {"versioned_ensembl_gene_id":"ENSG00000267188.1","gene_symbol":"AC245748.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":44392439,"end":44448452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248296.1","gene_symbol":"AC025465.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124492775,"end":124536348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228016.1","gene_symbol":"RAPGEF4-AS1","gene_name":"RAPGEF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28081]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"91149","summary":null,"start":172677141,"end":172736206,"strand":-1,"description":"RAPGEF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28081]"}, {"versioned_ensembl_gene_id":"ENSG00000038274.16","gene_symbol":"MAT2B","gene_name":"methionine adenosyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:6905]","synonyms":"SDR23E1,MATIIbeta","biotype":"protein_coding","ncbi_id":"27430","summary":"The protein encoded by this gene belongs to the methionine adenosyltransferase (MAT) family. MAT catalyzes the biosynthesis of S-adenosylmethionine from methionine and ATP. This protein is the regulatory beta subunit of MAT. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]","start":163503114,"end":163519336,"strand":1,"description":"methionine adenosyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:6905]"}, {"versioned_ensembl_gene_id":"ENSG00000233466.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30404517,"end":30409122,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000265185.5","gene_symbol":"SNORD3B-1","gene_name":"small nucleolar RNA, C/D box 3B-1 [Source:HGNC Symbol;Acc:HGNC:10168]","synonyms":"U3b2,U3b1,U3a,RNU3A1","biotype":"snoRNA","ncbi_id":"26851","summary":null,"start":19061912,"end":19062669,"strand":1,"description":"small nucleolar RNA, C/D box 3B-1 [Source:HGNC Symbol;Acc:HGNC:10168]"}, {"versioned_ensembl_gene_id":"ENSG00000185262.8","gene_symbol":"UBALD2","gene_name":"UBA like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28438]","synonyms":"MGC29814,FAM100B","biotype":"protein_coding","ncbi_id":"283991","summary":null,"start":76265202,"end":76271299,"strand":1,"description":"UBA like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28438]"}, {"versioned_ensembl_gene_id":"ENSG00000217377.1","gene_symbol":"AK4P5","gene_name":"adenylate kinase 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526416","summary":null,"start":80077729,"end":80078362,"strand":-1,"description":"adenylate kinase 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39068]"}, {"versioned_ensembl_gene_id":"ENSG00000228487.2","gene_symbol":"AL450263.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127213783,"end":127221907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218418.2","gene_symbol":"AL591135.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80064286,"end":80070199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272742.1","gene_symbol":"AC135457.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139364677,"end":139369717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267748.4","gene_symbol":"AC011479.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38289151,"end":38304910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258927.1","gene_symbol":"AL133467.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95620914,"end":95643285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228305.2","gene_symbol":"AC016734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63622178,"end":63622831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182512.4","gene_symbol":"GLRX5","gene_name":"glutaredoxin 5 [Source:HGNC Symbol;Acc:HGNC:20134]","synonyms":"PR01238,GRX5,C14orf87","biotype":"protein_coding","ncbi_id":"51218","summary":"This gene encodes a mitochondrial protein, which is evolutionarily conserved. It is involved in the biogenesis of iron-sulfur clusters, which are required for normal iron homeostasis. Mutations in this gene are associated with autosomal recessive pyridoxine-refractory sideroblastic anemia. [provided by RefSeq, May 2010]","start":95533503,"end":95544724,"strand":1,"description":"glutaredoxin 5 [Source:HGNC Symbol;Acc:HGNC:20134]"}, {"versioned_ensembl_gene_id":"ENSG00000233716.1","gene_symbol":"AC074367.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63232453,"end":63233577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185345.18","gene_symbol":"PRKN","gene_name":"parkin RBR E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:8607]","synonyms":"PDJ,parkin,PARK2,AR-JP","biotype":"protein_coding","ncbi_id":"5071","summary":"The precise function of this gene is unknown; however, the encoded protein is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. Mutations in this gene are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease. Alternative splicing of this gene produces multiple transcript variants encoding distinct isoforms. Additional splice variants of this gene have been described but currently lack transcript support. [provided by RefSeq, Jul 2008]","start":161347420,"end":162727771,"strand":-1,"description":"parkin RBR E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:8607]"}, {"versioned_ensembl_gene_id":"ENSG00000258844.1","gene_symbol":"AL162511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36214607,"end":36235608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279772.1","gene_symbol":"AC026422.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123508736,"end":123509187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276916.1","gene_symbol":"AL442125.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113511747,"end":113514473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206511.10","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"GPRC3A,hGB1a","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555518,"end":29633080,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000205002.3","gene_symbol":"AARD","gene_name":"alanine and arginine rich domain containing protein [Source:HGNC Symbol;Acc:HGNC:33842]","synonyms":"LOC441376,C8orf85","biotype":"protein_coding","ncbi_id":"441376","summary":null,"start":116938199,"end":116944487,"strand":1,"description":"alanine and arginine rich domain containing protein [Source:HGNC Symbol;Acc:HGNC:33842]"}, {"versioned_ensembl_gene_id":"ENSG00000278988.1","gene_symbol":"AL356490.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82543718,"end":82544196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232749.2","gene_symbol":"AL162726.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82451656,"end":82455225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182531.7","gene_symbol":"OR7E115P","gene_name":"olfactory receptor family 7 subfamily E member 115 pseudogene [Source:HGNC Symbol;Acc:HGNC:15127]","synonyms":"OST704","biotype":"unprocessed_pseudogene","ncbi_id":"81353","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15007861,"end":15008884,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 115 pseudogene [Source:HGNC Symbol;Acc:HGNC:15127]"}, {"versioned_ensembl_gene_id":"ENSG00000227728.2","gene_symbol":"AL356583.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":246509038,"end":246522592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211959.2","gene_symbol":"IGHV4-39","gene_name":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28394","summary":null,"start":106421711,"end":106422218,"strand":-1,"description":"immunoglobulin heavy variable 4-39 [Source:HGNC Symbol;Acc:HGNC:5651]"}, {"versioned_ensembl_gene_id":"ENSG00000204850.4","gene_symbol":"AC011484.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46494508,"end":46496502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253359.1","gene_symbol":"IGHV3-37","gene_name":"immunoglobulin heavy variable 3-37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5600]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28430","summary":null,"start":106396676,"end":106397114,"strand":-1,"description":"immunoglobulin heavy variable 3-37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5600]"}, {"versioned_ensembl_gene_id":"ENSG00000211957.2","gene_symbol":"IGHV3-35","gene_name":"immunoglobulin heavy variable 3-35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5598]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28432","summary":null,"start":106389392,"end":106389858,"strand":-1,"description":"immunoglobulin heavy variable 3-35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5598]"}, {"versioned_ensembl_gene_id":"ENSG00000274937.1","gene_symbol":"AC090826.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74374678,"end":74375511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125285.5","gene_symbol":"SOX21","gene_name":"SRY-box 21 [Source:HGNC Symbol;Acc:HGNC:11197]","synonyms":"SOX25","biotype":"protein_coding","ncbi_id":"11166","summary":"SRY-related HMG-box (SOX) genes encode a family of DNA-binding proteins containing a 79-amino acid HMG (high mobility group) domain that shares at least 50% sequence identity with the DNA-binding HMG box of the SRY protein (MIM 480000). SOX proteins are divided into 6 subgroups based on sequence similarity within and outside of the HMG domain. For additional background information on SOX genes, see SOX1 (MIM 602148).[supplied by OMIM, Apr 2004]","start":94709622,"end":94712399,"strand":-1,"description":"SRY-box 21 [Source:HGNC Symbol;Acc:HGNC:11197]"}, {"versioned_ensembl_gene_id":"ENSG00000269811.2","gene_symbol":"SCGB2B3P","gene_name":"secretoglobin family 2B member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:31895]","synonyms":"SCGB4A3P,C2B","biotype":"processed_pseudogene","ncbi_id":"100130342","summary":null,"start":34645662,"end":34646070,"strand":1,"description":"secretoglobin family 2B member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:31895]"}, {"versioned_ensembl_gene_id":"ENSG00000237054.9","gene_symbol":"PRMT5-AS1","gene_name":"PRMT5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40533]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505758","summary":null,"start":22918947,"end":22926900,"strand":1,"description":"PRMT5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40533]"}, {"versioned_ensembl_gene_id":"ENSG00000273719.1","gene_symbol":"AL359547.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146638844,"end":146639261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268027.5","gene_symbol":"AC243960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41545192,"end":41555462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250519.6","gene_symbol":"AP002784.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94238150,"end":94279206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270164.1","gene_symbol":"LINC01480","gene_name":"long intergenic non-protein coding RNA 1480 [Source:HGNC Symbol;Acc:HGNC:51124]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927931","summary":null,"start":41535183,"end":41536904,"strand":1,"description":"long intergenic non-protein coding RNA 1480 [Source:HGNC Symbol;Acc:HGNC:51124]"}, {"versioned_ensembl_gene_id":"ENSG00000198382.8","gene_symbol":"UVRAG","gene_name":"UV radiation resistance associated [Source:HGNC Symbol;Acc:HGNC:12640]","synonyms":"VPS38","biotype":"protein_coding","ncbi_id":"7405","summary":"This gene complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells and encodes a protein with a C2 domain. The protein activates the Beclin1-PI(3)KC3 complex, promoting autophagy and suppressing the proliferation and tumorigenicity of human colon cancer cells. Chromosomal aberrations involving this gene are associated with left-right axis malformation and mutations in this gene have been associated with colon cancer. [provided by RefSeq, Jul 2008]","start":75815167,"end":76143195,"strand":1,"description":"UV radiation resistance associated [Source:HGNC Symbol;Acc:HGNC:12640]"}, {"versioned_ensembl_gene_id":"ENSG00000274922.1","gene_symbol":"AL139384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112686769,"end":112689815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268034.1","gene_symbol":"AC243960.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41506152,"end":41506898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172247.3","gene_symbol":"C1QTNF4","gene_name":"C1q and TNF related 4 [Source:HGNC Symbol;Acc:HGNC:14346]","synonyms":"ZACRP4,CTRP4","biotype":"protein_coding","ncbi_id":"114900","summary":null,"start":47589664,"end":47594659,"strand":-1,"description":"C1q and TNF related 4 [Source:HGNC Symbol;Acc:HGNC:14346]"}, {"versioned_ensembl_gene_id":"ENSG00000214784.4","gene_symbol":"AC010468.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111192226,"end":111193042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180376.16","gene_symbol":"CCDC66","gene_name":"coiled-coil domain containing 66 [Source:HGNC Symbol;Acc:HGNC:27709]","synonyms":"DKFZp686C0433","biotype":"protein_coding","ncbi_id":"285331","summary":null,"start":56557161,"end":56621818,"strand":1,"description":"coiled-coil domain containing 66 [Source:HGNC Symbol;Acc:HGNC:27709]"}, {"versioned_ensembl_gene_id":"ENSG00000269921.1","gene_symbol":"AC068620.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56387625,"end":56388153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198142.4","gene_symbol":"SOWAHC","gene_name":"sosondowah ankyrin repeat domain family member C [Source:HGNC Symbol;Acc:HGNC:26149]","synonyms":"FLJ21870,C2orf26,ANKRD57","biotype":"protein_coding","ncbi_id":"65124","summary":null,"start":109614334,"end":109618990,"strand":1,"description":"sosondowah ankyrin repeat domain family member C [Source:HGNC Symbol;Acc:HGNC:26149]"}, {"versioned_ensembl_gene_id":"ENSG00000255585.3","gene_symbol":"AL590627.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":137776539,"end":137789235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237934.1","gene_symbol":"AL590729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29223933,"end":29224816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085377.13","gene_symbol":"PREP","gene_name":"prolyl endopeptidase [Source:HGNC Symbol;Acc:HGNC:9358]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5550","summary":"The protein encoded by this gene is a cytosolic prolyl endopeptidase that cleaves peptide bonds on the C-terminal side of prolyl residues within peptides that are up to approximately 30 amino acids long. Prolyl endopeptidases have been reported to be involved in the maturation and degradation of peptide hormones and neuropeptides. [provided by RefSeq, Jul 2008]","start":105277565,"end":105403084,"strand":-1,"description":"prolyl endopeptidase [Source:HGNC Symbol;Acc:HGNC:9358]"}, {"versioned_ensembl_gene_id":"ENSG00000128886.11","gene_symbol":"ELL3","gene_name":"elongation factor for RNA polymerase II 3 [Source:HGNC Symbol;Acc:HGNC:23113]","synonyms":"FLJ22637","biotype":"protein_coding","ncbi_id":"80237","summary":null,"start":43772600,"end":43777543,"strand":-1,"description":"elongation factor for RNA polymerase II 3 [Source:HGNC Symbol;Acc:HGNC:23113]"}, {"versioned_ensembl_gene_id":"ENSG00000119973.5","gene_symbol":"PRLHR","gene_name":"prolactin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4464]","synonyms":"PrRPR,GPR10","biotype":"protein_coding","ncbi_id":"2834","summary":"PRLHR is a 7-transmembrane domain receptor for prolactin-releasing hormone (PRLH; MIM 602663) that is highly expressed in anterior pituitary (Ozawa et al., 2002 [PubMed 11923475]).[supplied by OMIM, Mar 2008]","start":118589989,"end":118595699,"strand":-1,"description":"prolactin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4464]"}, {"versioned_ensembl_gene_id":"ENSG00000231973.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"HS6M1-14,OR2I2,OR2I4P,OR2I1,OR2I3P","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29553124,"end":29554071,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000187003.6","gene_symbol":"ACTL7A","gene_name":"actin like 7A [Source:HGNC Symbol;Acc:HGNC:161]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10881","summary":"The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7A), and related gene, ACTL7B, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7A gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. The ACTL7A gene is expressed in a wide variety of adult tissues, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":108862266,"end":108863759,"strand":1,"description":"actin like 7A [Source:HGNC Symbol;Acc:HGNC:161]"}, {"versioned_ensembl_gene_id":"ENSG00000173406.15","gene_symbol":"DAB1","gene_name":"DAB1, reelin adaptor protein [Source:HGNC Symbol;Acc:HGNC:2661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1600","summary":"The laminar organization of multiple neuronal types in the cerebral cortex is required for normal cognitive function. In mice, the disabled-1 gene plays a central role in brain development, directing the migration of cortical neurons past previously formed neurons to reach their proper layer. This gene is similar to disabled-1, and the protein encoded by this gene is thought to be a signal transducer that interacts with protein kinase pathways to regulate neuronal positioning in the developing brain. [provided by RefSeq, Jan 2017]","start":56994778,"end":58546734,"strand":-1,"description":"DAB1, reelin adaptor protein [Source:HGNC Symbol;Acc:HGNC:2661]"}, {"versioned_ensembl_gene_id":"ENSG00000230564.1","gene_symbol":"CALM1P2","gene_name":"calmodulin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1444]","synonyms":"TCAG_1643085","biotype":"processed_pseudogene","ncbi_id":"804","summary":null,"start":55259809,"end":55260256,"strand":-1,"description":"calmodulin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1444]"}, {"versioned_ensembl_gene_id":"ENSG00000227350.1","gene_symbol":"AL389915.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107543151,"end":107543616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236888.1","gene_symbol":"RPS20P5","gene_name":"ribosomal protein S20 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36367]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270899","summary":null,"start":57605847,"end":57606206,"strand":-1,"description":"ribosomal protein S20 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36367]"}, {"versioned_ensembl_gene_id":"ENSG00000261819.1","gene_symbol":"AC138932.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14988259,"end":14990160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244437.1","gene_symbol":"IGKV3-15","gene_name":"immunoglobulin kappa variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5816]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28913","summary":null,"start":89085177,"end":89085787,"strand":-1,"description":"immunoglobulin kappa variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5816]"}, {"versioned_ensembl_gene_id":"ENSG00000258039.2","gene_symbol":"AC117377.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99093359,"end":99105011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196743.8","gene_symbol":"GM2A","gene_name":"GM2 ganglioside activator [Source:HGNC Symbol;Acc:HGNC:4367]","synonyms":"SAP-3","biotype":"protein_coding","ncbi_id":"2760","summary":"This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":151212150,"end":151270440,"strand":1,"description":"GM2 ganglioside activator [Source:HGNC Symbol;Acc:HGNC:4367]"}, {"versioned_ensembl_gene_id":"ENSG00000266714.7","gene_symbol":"MYO15B","gene_name":"myosin XVB [Source:HGNC Symbol;Acc:HGNC:14083]","synonyms":"MYO15BP","biotype":"protein_coding","ncbi_id":"80022","summary":null,"start":75588058,"end":75626501,"strand":1,"description":"myosin XVB [Source:HGNC Symbol;Acc:HGNC:14083]"}, {"versioned_ensembl_gene_id":"ENSG00000085721.12","gene_symbol":"RRN3","gene_name":"RRN3 homolog, RNA polymerase I transcription factor [Source:HGNC Symbol;Acc:HGNC:30346]","synonyms":"DKFZp566E104,TIF-IA","biotype":"protein_coding","ncbi_id":"54700","summary":null,"start":15060022,"end":15094317,"strand":-1,"description":"RRN3 homolog, RNA polymerase I transcription factor [Source:HGNC Symbol;Acc:HGNC:30346]"}, {"versioned_ensembl_gene_id":"ENSG00000173805.15","gene_symbol":"HAP1","gene_name":"huntingtin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:4812]","synonyms":"HLP,HIP5,hHLP1,HAP2","biotype":"protein_coding","ncbi_id":"9001","summary":"Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":41717742,"end":41734644,"strand":-1,"description":"huntingtin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:4812]"}, {"versioned_ensembl_gene_id":"ENSG00000171714.10","gene_symbol":"ANO5","gene_name":"anoctamin 5 [Source:HGNC Symbol;Acc:HGNC:27337]","synonyms":"TMEM16E,LGMD2L,GDD1","biotype":"protein_coding","ncbi_id":"203859","summary":"This gene encodes a member of the anoctamin family of transmembrane proteins. The encoded protein is likely a calcium activated chloride channel. Mutations in this gene have been associated with gnathodiaphyseal dysplasia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2009]","start":22193176,"end":22283357,"strand":1,"description":"anoctamin 5 [Source:HGNC Symbol;Acc:HGNC:27337]"}, {"versioned_ensembl_gene_id":"ENSG00000253692.3","gene_symbol":"IGHEP1","gene_name":"immunoglobulin heavy constant epsilon P1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5523]","synonyms":null,"biotype":"IG_C_pseudogene","ncbi_id":"3498","summary":null,"start":105721794,"end":105722527,"strand":-1,"description":"immunoglobulin heavy constant epsilon P1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5523]"}, {"versioned_ensembl_gene_id":"ENSG00000241755.1","gene_symbol":"IGKV1-9","gene_name":"immunoglobulin kappa variable 1-9 [Source:HGNC Symbol;Acc:HGNC:5744]","synonyms":"L8,IGKV19","biotype":"IG_V_gene","ncbi_id":"28941","summary":null,"start":89009982,"end":89010515,"strand":-1,"description":"immunoglobulin kappa variable 1-9 [Source:HGNC Symbol;Acc:HGNC:5744]"}, {"versioned_ensembl_gene_id":"ENSG00000228567.3","gene_symbol":"VN1R4","gene_name":"vomeronasal 1 receptor 4 [Source:HGNC Symbol;Acc:HGNC:19871]","synonyms":"V1RL4","biotype":"protein_coding","ncbi_id":"317703","summary":null,"start":53266676,"end":53267723,"strand":-1,"description":"vomeronasal 1 receptor 4 [Source:HGNC Symbol;Acc:HGNC:19871]"}, {"versioned_ensembl_gene_id":"ENSG00000240671.4","gene_symbol":"IGKV1-8","gene_name":"immunoglobulin kappa variable 1-8 [Source:HGNC Symbol;Acc:HGNC:5743]","synonyms":"L9,IGKV18","biotype":"IG_V_gene","ncbi_id":"28942","summary":null,"start":88992409,"end":88992931,"strand":-1,"description":"immunoglobulin kappa variable 1-8 [Source:HGNC Symbol;Acc:HGNC:5743]"}, {"versioned_ensembl_gene_id":"ENSG00000211895.5","gene_symbol":"IGHA1","gene_name":"immunoglobulin heavy constant alpha 1 [Source:HGNC Symbol;Acc:HGNC:5478]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3493","summary":null,"start":105703995,"end":105708665,"strand":-1,"description":"immunoglobulin heavy constant alpha 1 [Source:HGNC Symbol;Acc:HGNC:5478]"}, {"versioned_ensembl_gene_id":"ENSG00000278898.1","gene_symbol":"AC087045.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134764809,"end":134767276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258933.1","gene_symbol":"LINC02279","gene_name":"long intergenic non-protein coding RNA 2279 [Source:HGNC Symbol;Acc:HGNC:53195]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984637","summary":null,"start":94960277,"end":94962976,"strand":-1,"description":"long intergenic non-protein coding RNA 2279 [Source:HGNC Symbol;Acc:HGNC:53195]"}, {"versioned_ensembl_gene_id":"ENSG00000121236.20","gene_symbol":"TRIM6","gene_name":"tripartite motif containing 6 [Source:HGNC Symbol;Acc:HGNC:16277]","synonyms":"RNF89","biotype":"protein_coding","ncbi_id":"117854","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, B-box type 1 and B-box type 2 domain, and a coiled-coil region. The protein localizes to the nucleus, but its specific function has not been identified. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. Alternative splicing results in multiple transcript variants. A read-through transcript from this gene into the downstream TRIM34 gene has also been observed, which results in a fusion product from these neighboring family members. [provided by RefSeq, Oct 2010]","start":5596109,"end":5612958,"strand":1,"description":"tripartite motif containing 6 [Source:HGNC Symbol;Acc:HGNC:16277]"}, {"versioned_ensembl_gene_id":"ENSG00000235377.1","gene_symbol":"AL158047.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82130752,"end":82131632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113494.16","gene_symbol":"PRLR","gene_name":"prolactin receptor [Source:HGNC Symbol;Acc:HGNC:9446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5618","summary":"This gene encodes a receptor for the anterior pituitary hormone, prolactin, and belongs to the type I cytokine receptor family. Prolactin-dependent signaling occurs as the result of ligand-induced dimerization of the prolactin receptor. Several alternatively spliced transcript variants encoding different membrane-bound and soluble isoforms have been described for this gene, which may function to modulate the endocrine and autocrine effects of prolactin in normal tissue and cancer. [provided by RefSeq, Feb 2011]","start":35048756,"end":35230589,"strand":-1,"description":"prolactin receptor [Source:HGNC Symbol;Acc:HGNC:9446]"}, {"versioned_ensembl_gene_id":"ENSG00000258011.2","gene_symbol":"AC144548.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110429959,"end":110430282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231668.2","gene_symbol":"PPP2R2DP1","gene_name":"protein phosphatase 2 regulatory subunit Bdelta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100327036","summary":null,"start":38051759,"end":38052395,"strand":1,"description":"protein phosphatase 2 regulatory subunit Bdelta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44544]"}, {"versioned_ensembl_gene_id":"ENSG00000276791.1","gene_symbol":"AC092117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2777319,"end":2780568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184321.1","gene_symbol":"OR51J1","gene_name":"olfactory receptor family 51 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14856]","synonyms":"OR51J2,OR51J1P","biotype":"protein_coding","ncbi_id":"79470","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":5402597,"end":5403547,"strand":1,"description":"olfactory receptor family 51 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14856]"}, {"versioned_ensembl_gene_id":"ENSG00000236359.1","gene_symbol":"OR51B8P","gene_name":"olfactory receptor family 51 subfamily B member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:31279]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403266","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5330592,"end":5331360,"strand":-1,"description":"olfactory receptor family 51 subfamily B member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:31279]"}, {"versioned_ensembl_gene_id":"ENSG00000171532.4","gene_symbol":"NEUROD2","gene_name":"neuronal differentiation 2 [Source:HGNC Symbol;Acc:HGNC:7763]","synonyms":"NDRF,bHLHa1","biotype":"protein_coding","ncbi_id":"4761","summary":"This gene encodes a member of the neuroD family of neurogenic basic helix-loop-helix (bHLH) proteins. Expression of this gene can induce transcription from neuron-specific promoters, such as the GAP-43 promoter, which contain a specific DNA sequence known as an E-box. The product of the human gene can induce neurogenic differentiation in non-neuronal cells in Xenopus embryos, and is thought to play a role in the determination and maintenance of neuronal cell fates. [provided by RefSeq, Jul 2008]","start":39603536,"end":39609777,"strand":-1,"description":"neuronal differentiation 2 [Source:HGNC Symbol;Acc:HGNC:7763]"}, {"versioned_ensembl_gene_id":"ENSG00000198384.8","gene_symbol":"TPTE2P3","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27345]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"220115","summary":null,"start":52522632,"end":52586906,"strand":1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27345]"}, {"versioned_ensembl_gene_id":"ENSG00000170345.9","gene_symbol":"FOS","gene_name":"Fos proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3796]","synonyms":"c-fos,AP-1","biotype":"protein_coding","ncbi_id":"2353","summary":"The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. In some cases, expression of the FOS gene has also been associated with apoptotic cell death. [provided by RefSeq, Jul 2008]","start":75278774,"end":75282230,"strand":1,"description":"Fos proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3796]"}, {"versioned_ensembl_gene_id":"ENSG00000174453.9","gene_symbol":"VWC2L","gene_name":"von Willebrand factor C domain containing protein 2 like [Source:HGNC Symbol;Acc:HGNC:37203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402117","summary":null,"start":214411065,"end":214578959,"strand":1,"description":"von Willebrand factor C domain containing protein 2 like [Source:HGNC Symbol;Acc:HGNC:37203]"}, {"versioned_ensembl_gene_id":"ENSG00000273526.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832771,"end":54848624,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000154277.12","gene_symbol":"UCHL1","gene_name":"ubiquitin C-terminal hydrolase L1 [Source:HGNC Symbol;Acc:HGNC:12513]","synonyms":"Uch-L1,PGP9.5,PARK5","biotype":"protein_coding","ncbi_id":"7345","summary":"The protein encoded by this gene belongs to the peptidase C12 family. This enzyme is a thiol protease that hydrolyzes a peptide bond at the C-terminal glycine of ubiquitin. This gene is specifically expressed in the neurons and in cells of the diffuse neuroendocrine system. Mutations in this gene may be associated with Parkinson disease.[provided by RefSeq, Sep 2009]","start":41256413,"end":41268455,"strand":1,"description":"ubiquitin C-terminal hydrolase L1 [Source:HGNC Symbol;Acc:HGNC:12513]"}, {"versioned_ensembl_gene_id":"ENSG00000211716.2","gene_symbol":"TRBV9","gene_name":"T-cell receptor beta variable 9 [Source:HGNC Symbol;Acc:HGNC:12246]","synonyms":"TCRBV1S1A1N1,TCRBV9S1","biotype":"TR_V_gene","ncbi_id":"28586","summary":null,"start":142391891,"end":142392412,"strand":1,"description":"T-cell receptor beta variable 9 [Source:HGNC Symbol;Acc:HGNC:12246]"}, {"versioned_ensembl_gene_id":"ENSG00000196510.12","gene_symbol":"ANAPC7","gene_name":"anaphase promoting complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:17380]","synonyms":"APC7","biotype":"protein_coding","ncbi_id":"51434","summary":"This gene encodes a tetratricopeptide repeat containing component of the anaphase promoting complex/cyclosome (APC/C), a large E3 ubiquitin ligase that controls cell cycle progression by targeting a number of cell cycle regulators such as B-type cyclins for 26S proteasome-mediated degradation through ubiquitination. The encoded protein is required for proper protein ubiquitination function of APC/C and for the interaction of APC/C with certain transcription coactivators. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":110372900,"end":110403730,"strand":-1,"description":"anaphase promoting complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:17380]"}, {"versioned_ensembl_gene_id":"ENSG00000197043.13","gene_symbol":"ANXA6","gene_name":"annexin A6 [Source:HGNC Symbol;Acc:HGNC:544]","synonyms":"ANX6","biotype":"protein_coding","ncbi_id":"309","summary":"Annexin VI belongs to a family of calcium-dependent membrane and phospholipid binding proteins. Several members of the annexin family have been implicated in membrane-related events along exocytotic and endocytotic pathways. The annexin VI gene is approximately 60 kbp long and contains 26 exons. It encodes a protein of about 68 kDa that consists of eight 68-amino acid repeats separated by linking sequences of variable lengths. It is highly similar to human annexins I and II sequences, each of which contain four such repeats. Annexin VI has been implicated in mediating the endosome aggregation and vesicle fusion in secreting epithelia during exocytosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2010]","start":151100712,"end":151157882,"strand":-1,"description":"annexin A6 [Source:HGNC Symbol;Acc:HGNC:544]"}, {"versioned_ensembl_gene_id":"ENSG00000109917.10","gene_symbol":"ZPR1","gene_name":"ZPR1 zinc finger [Source:HGNC Symbol;Acc:HGNC:13051]","synonyms":"ZNF259","biotype":"protein_coding","ncbi_id":"8882","summary":"The protein encoded by this gene is found in the cytoplasm of quiescent cells but translocates to the nucleolus in proliferating cells. The encoded protein interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth. Defects in this gene or the SMN1 gene can cause spinal muscular atrophy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":116773799,"end":116788050,"strand":-1,"description":"ZPR1 zinc finger [Source:HGNC Symbol;Acc:HGNC:13051]"}, {"versioned_ensembl_gene_id":"ENSG00000235480.1","gene_symbol":"AC013270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96527940,"end":96532306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224682.1","gene_symbol":"SOCS5P2","gene_name":"suppressor of cytokine signaling 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128299","summary":null,"start":135447446,"end":135450154,"strand":1,"description":"suppressor of cytokine signaling 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44598]"}, {"versioned_ensembl_gene_id":"ENSG00000272418.1","gene_symbol":"AC090607.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":78280950,"end":78282190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244259.1","gene_symbol":"AP000797.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115950196,"end":115950801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251675.1","gene_symbol":"AC010260.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80128361,"end":80143883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257067.5","gene_symbol":"AP000797.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115932774,"end":115942995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277482.1","gene_symbol":"AC090607.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78299701,"end":78299924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259322.1","gene_symbol":"AC090607.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78293286,"end":78296049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273565.1","gene_symbol":"AL691403.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75176929,"end":75177418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267191.1","gene_symbol":"AC006213.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43902001,"end":43926545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279375.1","gene_symbol":"AC244517.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141191599,"end":141194088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226962.1","gene_symbol":"RAC1P6","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422657","summary":null,"start":115136475,"end":115137220,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42006]"}, {"versioned_ensembl_gene_id":"ENSG00000130307.11","gene_symbol":"USHBP1","gene_name":"USH1 protein network component harmonin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24058]","synonyms":"MCC2,FLJ38709,AIEBP","biotype":"protein_coding","ncbi_id":"83878","summary":null,"start":17249176,"end":17282786,"strand":-1,"description":"USH1 protein network component harmonin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24058]"}, {"versioned_ensembl_gene_id":"ENSG00000188293.5","gene_symbol":"IGFL1","gene_name":"IGF like family member 1 [Source:HGNC Symbol;Acc:HGNC:24093]","synonyms":"UNQ644","biotype":"protein_coding","ncbi_id":"374918","summary":"The protein encoded by this gene is a member of the insulin-like growth factor family of signaling molecules. The encoded protein is synthesized as a precursor protein and is proteolytically cleaved to form a secreted mature peptide. The mature peptide binds to a receptor, which in mouse was found on the cell surface of T cells. Increased expression of this gene may be linked to psoriasis. [provided by RefSeq, Aug 2016]","start":46229752,"end":46231243,"strand":1,"description":"IGF like family member 1 [Source:HGNC Symbol;Acc:HGNC:24093]"}, {"versioned_ensembl_gene_id":"ENSG00000233114.2","gene_symbol":"AL358075.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46104950,"end":46105175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278139.1","gene_symbol":"AL358075.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46043661,"end":46176488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176043.5","gene_symbol":"AC007160.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72929612,"end":72929930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226252.1","gene_symbol":"AL135960.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47225797,"end":47230750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274492.1","gene_symbol":"AL121768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88819608,"end":88822151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279558.1","gene_symbol":"AC244517.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141078076,"end":141084481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153094.22","gene_symbol":"BCL2L11","gene_name":"BCL2 like 11 [Source:HGNC Symbol;Acc:HGNC:994]","synonyms":"BOD,BimS,BimL,BimEL,BIM","biotype":"protein_coding","ncbi_id":"10018","summary":"The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The protein encoded by this gene contains a Bcl-2 homology domain 3 (BH3). It has been shown to interact with other members of the BCL-2 protein family and to act as an apoptotic activator. The expression of this gene can be induced by nerve growth factor (NGF), as well as by the forkhead transcription factor FKHR-L1, which suggests a role of this gene in neuronal and lymphocyte apoptosis. Transgenic studies of the mouse counterpart suggested that this gene functions as an essential initiator of apoptosis in thymocyte-negative selection. Several alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2013]","start":111119378,"end":111168447,"strand":1,"description":"BCL2 like 11 [Source:HGNC Symbol;Acc:HGNC:994]"}, {"versioned_ensembl_gene_id":"ENSG00000234625.1","gene_symbol":"LINC00380","gene_name":"long intergenic non-protein coding RNA 380 [Source:HGNC Symbol;Acc:HGNC:42706]","synonyms":"TCONS_00021685","biotype":"lincRNA","ncbi_id":"101930747","summary":null,"start":91087254,"end":91089593,"strand":-1,"description":"long intergenic non-protein coding RNA 380 [Source:HGNC Symbol;Acc:HGNC:42706]"}, {"versioned_ensembl_gene_id":"ENSG00000186832.8","gene_symbol":"KRT16","gene_name":"keratin 16 [Source:HGNC Symbol;Acc:HGNC:6423]","synonyms":"NEPPK","biotype":"protein_coding","ncbi_id":"3868","summary":"The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12-q21. This keratin has been coexpressed with keratin 14 in a number of epithelial tissues, including esophagus, tongue, and hair follicles. Mutations in this gene are associated with type 1 pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus. [provided by RefSeq, Jul 2008]","start":41609778,"end":41615899,"strand":-1,"description":"keratin 16 [Source:HGNC Symbol;Acc:HGNC:6423]"}, {"versioned_ensembl_gene_id":"ENSG00000215131.10","gene_symbol":"C16orf90","gene_name":"chromosome 16 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:34455]","synonyms":"LOC646174","biotype":"protein_coding","ncbi_id":"646174","summary":null,"start":3493484,"end":3495480,"strand":-1,"description":"chromosome 16 open reading frame 90 [Source:HGNC Symbol;Acc:HGNC:34455]"}, {"versioned_ensembl_gene_id":"ENSG00000153574.8","gene_symbol":"RPIA","gene_name":"ribose 5-phosphate isomerase A [Source:HGNC Symbol;Acc:HGNC:10297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22934","summary":"The protein encoded by this gene is an enzyme, which catalyzes the reversible conversion between ribose-5-phosphate and ribulose-5-phosphate in the pentose-phosphate pathway. This gene is highly conserved in most organisms. The enzyme plays an essential role in the carbohydrate metabolism. Mutations in this gene cause ribose 5-phosphate isomerase deficiency. A pseudogene is found on chromosome 18. [provided by RefSeq, Mar 2010]","start":88691644,"end":88750935,"strand":1,"description":"ribose 5-phosphate isomerase A [Source:HGNC Symbol;Acc:HGNC:10297]"}, {"versioned_ensembl_gene_id":"ENSG00000251603.1","gene_symbol":"AC092611.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151667224,"end":151670502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159217.9","gene_symbol":"IGF2BP1","gene_name":"insulin like growth factor 2 mRNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:28866]","synonyms":"IMP-1","biotype":"protein_coding","ncbi_id":"10642","summary":"This gene encodes a member of the insulin-like growth factor 2 mRNA-binding protein family. The protein encoded by this gene contains four K homology domains and two RNA recognition motifs. It functions by binding to the mRNAs of certain genes, including insulin-like growth factor 2, beta-actin and beta-transducin repeat-containing protein, and regulating their translation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":48997412,"end":49055650,"strand":1,"description":"insulin like growth factor 2 mRNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:28866]"}, {"versioned_ensembl_gene_id":"ENSG00000186847.5","gene_symbol":"KRT14","gene_name":"keratin 14 [Source:HGNC Symbol;Acc:HGNC:6416]","synonyms":"EBS4,EBS3","biotype":"protein_coding","ncbi_id":"3861","summary":"This gene encodes a member of the keratin family, the most diverse group of intermediate filaments. This gene product, a type I keratin, is usually found as a heterotetramer with two keratin 5 molecules, a type II keratin. Together they form the cytoskeleton of epithelial cells. Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex. At least one pseudogene has been identified at 17p12-p11. [provided by RefSeq, Jul 2008]","start":41582279,"end":41586921,"strand":-1,"description":"keratin 14 [Source:HGNC Symbol;Acc:HGNC:6416]"}, {"versioned_ensembl_gene_id":"ENSG00000005810.17","gene_symbol":"MYCBP2","gene_name":"MYC binding protein 2, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:23386]","synonyms":"PAM,KIAA0916,FLJ10106","biotype":"protein_coding","ncbi_id":"23077","summary":"This gene encodes an E3 ubiquitin-protein ligase and member of the PHR (Phr1/MYCBP2, highwire and RPM-1) family of proteins. The encoded protein plays a role in axon guidance and synapse formation in the developing nervous system. In mammalian cells, this protein regulates the cAMP and mTOR signaling pathways, and may additionally regulate autophagy. Reduced expression of this gene has been observed in acute lymphoblastic leukemia patients and a mutation in this gene has been identified in patients with a rare inherited vision defect. [provided by RefSeq, Mar 2017]","start":77044655,"end":77327050,"strand":-1,"description":"MYC binding protein 2, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:23386]"}, {"versioned_ensembl_gene_id":"ENSG00000162407.8","gene_symbol":"PLPP3","gene_name":"phospholipid phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:9229]","synonyms":"PPAP2B,PAP-2b,LPP3","biotype":"protein_coding","ncbi_id":"8613","summary":"The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. This protein is a membrane glycoprotein localized at the cell plasma membrane. It has been shown to actively hydrolyze extracellular lysophosphatidic acid and short-chain phosphatidic acid. The expression of this gene is found to be enhanced by epidermal growth factor in Hela cells. [provided by RefSeq, Mar 2010]","start":56494747,"end":56645301,"strand":-1,"description":"phospholipid phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:9229]"}, {"versioned_ensembl_gene_id":"ENSG00000229871.1","gene_symbol":"RPSAP20","gene_name":"ribosomal protein SA pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35595]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"127406","summary":null,"start":56207567,"end":56208456,"strand":-1,"description":"ribosomal protein SA pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35595]"}, {"versioned_ensembl_gene_id":"ENSG00000149289.10","gene_symbol":"ZC3H12C","gene_name":"zinc finger CCCH-type containing 12C [Source:HGNC Symbol;Acc:HGNC:29362]","synonyms":"MCPIP3,KIAA1726","biotype":"protein_coding","ncbi_id":"85463","summary":null,"start":110093361,"end":110171841,"strand":1,"description":"zinc finger CCCH-type containing 12C [Source:HGNC Symbol;Acc:HGNC:29362]"}, {"versioned_ensembl_gene_id":"ENSG00000278112.1","gene_symbol":"AC145423.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123519390,"end":123519856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258449.1","gene_symbol":"AC023510.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25096868,"end":25100980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135940.6","gene_symbol":"COX5B","gene_name":"cytochrome c oxidase subunit 5B [Source:HGNC Symbol;Acc:HGNC:2269]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1329","summary":"Cytochrome C oxidase (COX) is the terminal enzyme of the mitochondrial respiratory chain. It is a multi-subunit enzyme complex that couples the transfer of electrons from cytochrome c to molecular oxygen and contributes to a proton electrochemical gradient across the inner mitochondrial membrane. The complex consists of 13 mitochondrial- and nuclear-encoded subunits. The mitochondrially-encoded subunits perform the electron transfer and proton pumping activities. The functions of the nuclear-encoded subunits are unknown but they may play a role in the regulation and assembly of the complex. This gene encodes the nuclear-encoded subunit Vb of the human mitochondrial respiratory chain enzyme. [provided by RefSeq, Jul 2008]","start":97646040,"end":97648383,"strand":1,"description":"cytochrome c oxidase subunit 5B [Source:HGNC Symbol;Acc:HGNC:2269]"}, {"versioned_ensembl_gene_id":"ENSG00000270993.1","gene_symbol":"AC111186.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75060491,"end":75060620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279696.1","gene_symbol":"AP001273.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93726654,"end":93729805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145864.12","gene_symbol":"GABRB2","gene_name":"gamma-aminobutyric acid type A receptor beta2 subunit [Source:HGNC Symbol;Acc:HGNC:4082]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2561","summary":"The gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes GABA A receptor, beta 2 subunit. It is mapped to chromosome 5q34 in a cluster comprised of genes encoding alpha 1 and gamma 2 subunits of the GABA A receptor. Alternative splicing of this gene generates 2 transcript variants, differing by a 114 bp insertion. [provided by RefSeq, Jul 2008]","start":161288429,"end":161549044,"strand":-1,"description":"gamma-aminobutyric acid type A receptor beta2 subunit [Source:HGNC Symbol;Acc:HGNC:4082]"}, {"versioned_ensembl_gene_id":"ENSG00000215126.10","gene_symbol":"CBWD6","gene_name":"COBW domain containing 6 [Source:HGNC Symbol;Acc:HGNC:31978]","synonyms":"CBWD7,OTTHUMG00000067194,OTTHUMG00000066820","biotype":"protein_coding","ncbi_id":"644019","summary":null,"start":41131306,"end":41199261,"strand":-1,"description":"COBW domain containing 6 [Source:HGNC Symbol;Acc:HGNC:31978]"}, {"versioned_ensembl_gene_id":"ENSG00000284057.1","gene_symbol":"AP001273.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":93741664,"end":93812378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183323.12","gene_symbol":"CCDC125","gene_name":"coiled-coil domain containing 125 [Source:HGNC Symbol;Acc:HGNC:28924]","synonyms":"KENAE","biotype":"protein_coding","ncbi_id":"202243","summary":null,"start":69280175,"end":69332809,"strand":-1,"description":"coiled-coil domain containing 125 [Source:HGNC Symbol;Acc:HGNC:28924]"}, {"versioned_ensembl_gene_id":"ENSG00000218173.1","gene_symbol":"AL356967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104687241,"end":104687671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151247.12","gene_symbol":"EIF4E","gene_name":"eukaryotic translation initiation factor 4E [Source:HGNC Symbol;Acc:HGNC:3287]","synonyms":"EIF4F,EIF4EL1,EIF4E1","biotype":"protein_coding","ncbi_id":"1977","summary":"The protein encoded by this gene is a component of the eukaryotic translation initiation factor 4F complex, which recognizes the 7-methylguanosine cap structure at the 5' end of messenger RNAs. The encoded protein aids in translation initiation by recruiting ribosomes to the 5'-cap structure. Association of this protein with the 4F complex is the rate-limiting step in translation initiation. This gene acts as a proto-oncogene, and its expression and activation is associated with transformation and tumorigenesis. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":98871684,"end":98930637,"strand":-1,"description":"eukaryotic translation initiation factor 4E [Source:HGNC Symbol;Acc:HGNC:3287]"}, {"versioned_ensembl_gene_id":"ENSG00000157869.14","gene_symbol":"RAB28","gene_name":"RAB28, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9768]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9364","summary":"This gene encodes a member of the Rab subfamily of Ras-related small GTPases. The encoded protein may be involved in regulating intracellular trafficking. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 9 and X. [provided by RefSeq, Apr 2009]","start":13361354,"end":13484365,"strand":-1,"description":"RAB28, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9768]"}, {"versioned_ensembl_gene_id":"ENSG00000249476.1","gene_symbol":"AC008467.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109237120,"end":109326369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161281.10","gene_symbol":"COX7A1","gene_name":"cytochrome c oxidase subunit 7A1 [Source:HGNC Symbol;Acc:HGNC:2287]","synonyms":"COX7AH,COX7A","biotype":"protein_coding","ncbi_id":"1346","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 1 (muscle isoform) of subunit VIIa and the polypeptide 1 is present only in muscle tissues. Other polypeptides of subunit VIIa are present in both muscle and nonmuscle tissues, and are encoded by different genes. [provided by RefSeq, Jul 2008]","start":36150922,"end":36152869,"strand":-1,"description":"cytochrome c oxidase subunit 7A1 [Source:HGNC Symbol;Acc:HGNC:2287]"}, {"versioned_ensembl_gene_id":"ENSG00000254937.1","gene_symbol":"AP000916.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":124538500,"end":124539334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215199.3","gene_symbol":"YWHAZP6","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158383","summary":null,"start":34922184,"end":34922921,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30849]"}, {"versioned_ensembl_gene_id":"ENSG00000267308.1","gene_symbol":"LINC01764","gene_name":"long intergenic non-protein coding RNA 1764 [Source:HGNC Symbol;Acc:HGNC:52553]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372290","summary":null,"start":15827045,"end":15835853,"strand":-1,"description":"long intergenic non-protein coding RNA 1764 [Source:HGNC Symbol;Acc:HGNC:52553]"}, {"versioned_ensembl_gene_id":"ENSG00000267056.2","gene_symbol":"AC005336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15910582,"end":15911824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273330.1","gene_symbol":"CYP4F36P","gene_name":"cytochrome P450 family 4 subfamily F member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:42407]","synonyms":"CYP4F2-de12b","biotype":"unprocessed_pseudogene","ncbi_id":"100422235","summary":null,"start":15871667,"end":15871852,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:42407]"}, {"versioned_ensembl_gene_id":"ENSG00000248313.1","gene_symbol":"CYP4F27P","gene_name":"cytochrome P450 family 4 subfamily F member 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:39946]","synonyms":"CYP4F-se3[6:7:8]","biotype":"unprocessed_pseudogene","ncbi_id":"107133494","summary":null,"start":130048426,"end":130049440,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:39946]"}, {"versioned_ensembl_gene_id":"ENSG00000131196.17","gene_symbol":"NFATC1","gene_name":"nuclear factor of activated T-cells 1 [Source:HGNC Symbol;Acc:HGNC:7775]","synonyms":"NFATc,NFAT2,NF-ATC","biotype":"protein_coding","ncbi_id":"4772","summary":"The product of this gene is a component of the nuclear factor of activated T cells DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor (TCR) stimulation, and an inducible nuclear component. Proteins belonging to this family of transcription factors play a central role in inducible gene transcription during immune response. The product of this gene is an inducible nuclear component. It functions as a major molecular target for the immunosuppressive drugs such as cyclosporin A. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Different isoforms of this protein may regulate inducible expression of different cytokine genes. [provided by RefSeq, Jul 2013]","start":79395856,"end":79529325,"strand":1,"description":"nuclear factor of activated T-cells 1 [Source:HGNC Symbol;Acc:HGNC:7775]"}, {"versioned_ensembl_gene_id":"ENSG00000261702.2","gene_symbol":"AC022254.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67974391,"end":67974625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282352.1","gene_symbol":"ZNF965P","gene_name":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132598","summary":null,"start":18734080,"end":18734896,"strand":1,"description":"zinc finger protein 965, pseudogene [Source:HGNC Symbol;Acc:HGNC:42025]"}, {"versioned_ensembl_gene_id":"ENSG00000189043.9","gene_symbol":"NDUFA4","gene_name":"NDUFA4, mitochondrial complex associated [Source:HGNC Symbol;Acc:HGNC:7687]","synonyms":"MLRQ,CI-9k","biotype":"protein_coding","ncbi_id":"4697","summary":"The protein encoded by this gene belongs to the complex I 9kDa subunit family. Mammalian complex I of mitochondrial respiratory chain is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [provided by RefSeq, Jul 2008]","start":10931951,"end":10940256,"strand":-1,"description":"NDUFA4, mitochondrial complex associated [Source:HGNC Symbol;Acc:HGNC:7687]"}, {"versioned_ensembl_gene_id":"ENSG00000267661.1","gene_symbol":"AP001269.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11928838,"end":11929476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072133.10","gene_symbol":"RPS6KA6","gene_name":"ribosomal protein S6 kinase A6 [Source:HGNC Symbol;Acc:HGNC:10435]","synonyms":"RSK4","biotype":"protein_coding","ncbi_id":"27330","summary":"This gene encodes a member of ribosomal S6 kinase family, serine-threonine protein kinases which are regulated by growth factors. The encoded protein may be distinct from other members of this family, however, as studies suggest it is not growth factor dependent and may not participate in the same signaling pathways. [provided by RefSeq, Jan 2010]","start":84058346,"end":84187907,"strand":-1,"description":"ribosomal protein S6 kinase A6 [Source:HGNC Symbol;Acc:HGNC:10435]"}, {"versioned_ensembl_gene_id":"ENSG00000206535.7","gene_symbol":"LNP1","gene_name":"leukemia NUP98 fusion partner 1 [Source:HGNC Symbol;Acc:HGNC:28014]","synonyms":"NP3","biotype":"protein_coding","ncbi_id":"348801","summary":null,"start":100401193,"end":100456319,"strand":1,"description":"leukemia NUP98 fusion partner 1 [Source:HGNC Symbol;Acc:HGNC:28014]"}, {"versioned_ensembl_gene_id":"ENSG00000269445.1","gene_symbol":"AC067969.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38526954,"end":38528555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198765.11","gene_symbol":"SYCP1","gene_name":"synaptonemal complex protein 1 [Source:HGNC Symbol;Acc:HGNC:11487]","synonyms":"CT8,SCP1,HOM-TES-14","biotype":"protein_coding","ncbi_id":"6847","summary":null,"start":114854803,"end":114995370,"strand":1,"description":"synaptonemal complex protein 1 [Source:HGNC Symbol;Acc:HGNC:11487]"}, {"versioned_ensembl_gene_id":"ENSG00000130818.11","gene_symbol":"ZNF426","gene_name":"zinc finger protein 426 [Source:HGNC Symbol;Acc:HGNC:20725]","synonyms":"MGC2663","biotype":"protein_coding","ncbi_id":"79088","summary":"Kaposi's sarcoma-associated herpesvirus (KSHV) can be reactivated from latency by the viral protein RTA. The protein encoded by this gene is a zinc finger transcriptional repressor that interacts with RTA to modulate RTA-mediated reactivation of KSHV. While the encoded protein can repress KSHV reactivation, RTA can induce degradation of this protein through the ubiquitin-proteasome pathway to overcome the repression. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":9523224,"end":9538645,"strand":-1,"description":"zinc finger protein 426 [Source:HGNC Symbol;Acc:HGNC:20725]"}, {"versioned_ensembl_gene_id":"ENSG00000235986.9","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30531215,"end":30547013,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000236768.1","gene_symbol":"AC124916.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48120669,"end":48121215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265541.1","gene_symbol":"H3F3BP2","gene_name":"H3 histone, family 3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42979]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420410","summary":null,"start":28416922,"end":28417492,"strand":1,"description":"H3 histone, family 3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42979]"}, {"versioned_ensembl_gene_id":"ENSG00000186529.15","gene_symbol":"CYP4F3","gene_name":"cytochrome P450 family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:2646]","synonyms":"CYP4F,LTB4H","biotype":"protein_coding","ncbi_id":"4051","summary":"This gene, CYP4F3, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. The enzyme starts the process of inactivating and degrading leukotriene B4, a potent mediator of inflammation. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F8, is approximately 18 kb away. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Apr 2019]","start":15640897,"end":15662825,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 3 [Source:HGNC Symbol;Acc:HGNC:2646]"}, {"versioned_ensembl_gene_id":"ENSG00000101213.6","gene_symbol":"PTK6","gene_name":"protein tyrosine kinase 6 [Source:HGNC Symbol;Acc:HGNC:9617]","synonyms":"BRK","biotype":"protein_coding","ncbi_id":"5753","summary":"The protein encoded by this gene is a cytoplasmic nonreceptor protein kinase which may function as an intracellular signal transducer in epithelial tissues. Overexpression of this gene in mammary epithelial cells leads to sensitization of the cells to epidermal growth factor and results in a partially transformed phenotype. Expression of this gene has been detected at low levels in some breast tumors but not in normal breast tissue. The encoded protein has been shown to undergo autophosphorylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":63528001,"end":63537370,"strand":-1,"description":"protein tyrosine kinase 6 [Source:HGNC Symbol;Acc:HGNC:9617]"}, {"versioned_ensembl_gene_id":"ENSG00000205116.3","gene_symbol":"TMEM88B","gene_name":"transmembrane protein 88B [Source:HGNC Symbol;Acc:HGNC:37099]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643965","summary":null,"start":1426128,"end":1427787,"strand":1,"description":"transmembrane protein 88B [Source:HGNC Symbol;Acc:HGNC:37099]"}, {"versioned_ensembl_gene_id":"ENSG00000105255.10","gene_symbol":"FSD1","gene_name":"fibronectin type III and SPRY domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13745]","synonyms":"MIR1,MGC3213","biotype":"protein_coding","ncbi_id":"79187","summary":"This gene encodes a centrosome associated protein that is characterized by an N-terminal coiled-coil region downstream of B-box (BBC) domain, a central fibronectin type III domain, and a C-terminal repeats in splA and RyR (SPRY) domain. The encoded protein associates with a subset of microtubules and may be involved in the stability and organization of microtubules during cytokinesis. [provided by RefSeq, Apr 2009]","start":4304600,"end":4323843,"strand":1,"description":"fibronectin type III and SPRY domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13745]"}, {"versioned_ensembl_gene_id":"ENSG00000229031.1","gene_symbol":"MTCO1P25","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52090]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075167","summary":null,"start":69331835,"end":69333633,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52090]"}, {"versioned_ensembl_gene_id":"ENSG00000271857.1","gene_symbol":"AL096865.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45421079,"end":45422005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163655.15","gene_symbol":"GMPS","gene_name":"guanine monophosphate synthase [Source:HGNC Symbol;Acc:HGNC:4378]","synonyms":"GATD7","biotype":"protein_coding","ncbi_id":"8833","summary":"In the de novo synthesis of purine nucleotides, IMP is the branch point metabolite at which point the pathway diverges to the synthesis of either guanine or adenine nucleotides. In the guanine nucleotide pathway, there are 2 enzymes involved in converting IMP to GMP, namely IMP dehydrogenase (IMPD1), which catalyzes the oxidation of IMP to XMP, and GMP synthetase, which catalyzes the amination of XMP to GMP. [provided by RefSeq, Jul 2008]","start":155870536,"end":155944026,"strand":1,"description":"guanine monophosphate synthase [Source:HGNC Symbol;Acc:HGNC:4378]"}, {"versioned_ensembl_gene_id":"ENSG00000228176.1","gene_symbol":"AC092265.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29708851,"end":29709547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269904.2","gene_symbol":"MAP2K4P1","gene_name":"mitogen-activated protein kinase kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43837]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"139201","summary":null,"start":73524275,"end":73563085,"strand":-1,"description":"mitogen-activated protein kinase kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43837]"}, {"versioned_ensembl_gene_id":"ENSG00000237475.2","gene_symbol":"RPL7P53","gene_name":"ribosomal protein L7 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271145","summary":null,"start":73535503,"end":73536241,"strand":1,"description":"ribosomal protein L7 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36831]"}, {"versioned_ensembl_gene_id":"ENSG00000230470.1","gene_symbol":"AL078645.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":184408337,"end":184412360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279069.1","gene_symbol":"AC015813.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58006674,"end":58008187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166342.18","gene_symbol":"NETO1","gene_name":"neuropilin and tolloid like 1 [Source:HGNC Symbol;Acc:HGNC:13823]","synonyms":"BTCL1,BCTL1","biotype":"protein_coding","ncbi_id":"81832","summary":"This gene encodes a transmembrane protein containing two extracellular CUB domains followed by a low-density lipoprotein class A (LDLa) domain. This protein is thought to play a critical role in spatial learning and memory by regulating the function of synaptic N-methyl-D-aspartic acid receptor complexes in the hippocampus. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2017]","start":72742314,"end":72868146,"strand":-1,"description":"neuropilin and tolloid like 1 [Source:HGNC Symbol;Acc:HGNC:13823]"}, {"versioned_ensembl_gene_id":"ENSG00000197779.13","gene_symbol":"ZNF81","gene_name":"zinc finger protein 81 [Source:HGNC Symbol;Acc:HGNC:13156]","synonyms":"MRX45,HFZ20","biotype":"protein_coding","ncbi_id":"347344","summary":"This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017]","start":47836902,"end":48002561,"strand":1,"description":"zinc finger protein 81 [Source:HGNC Symbol;Acc:HGNC:13156]"}, {"versioned_ensembl_gene_id":"ENSG00000231884.1","gene_symbol":"NDUFB1P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30893]","synonyms":"NDUFB1P,bcm3095","biotype":"processed_pseudogene","ncbi_id":"100190952","summary":null,"start":48181547,"end":48181726,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30893]"}, {"versioned_ensembl_gene_id":"ENSG00000277459.1","gene_symbol":"AP001527.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102109827,"end":102110457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237014.1","gene_symbol":"AC004074.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73237647,"end":73238709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259091.1","gene_symbol":"LINC00517","gene_name":"long intergenic non-protein coding RNA 517 [Source:HGNC Symbol;Acc:HGNC:19831]","synonyms":"C14orf26","biotype":"antisense_RNA","ncbi_id":"400208","summary":null,"start":37896060,"end":37902372,"strand":-1,"description":"long intergenic non-protein coding RNA 517 [Source:HGNC Symbol;Acc:HGNC:19831]"}, {"versioned_ensembl_gene_id":"ENSG00000138311.15","gene_symbol":"ZNF365","gene_name":"zinc finger protein 365 [Source:HGNC Symbol;Acc:HGNC:18194]","synonyms":"UAN,KIAA0844","biotype":"protein_coding","ncbi_id":"22891","summary":"This gene encodes a zinc finger protein that may play a role in the repair of DNA damage and maintenance of genome stability. The N-terminal C2H2 zinc finger motif is required to form a protein complex with PARP1 and MRE11, which are known to be involved in the restart of stalled DNA replication forks. A mutation in this gene may be associated with breast cancer susceptibility. [provided by RefSeq, Mar 2020]","start":62374192,"end":62672011,"strand":1,"description":"zinc finger protein 365 [Source:HGNC Symbol;Acc:HGNC:18194]"}, {"versioned_ensembl_gene_id":"ENSG00000162878.12","gene_symbol":"PKDCC","gene_name":"protein kinase domain containing, cytoplasmic [Source:HGNC Symbol;Acc:HGNC:25123]","synonyms":"Vlk,SgK493","biotype":"protein_coding","ncbi_id":"91461","summary":null,"start":42048020,"end":42058528,"strand":1,"description":"protein kinase domain containing, cytoplasmic [Source:HGNC Symbol;Acc:HGNC:25123]"}, {"versioned_ensembl_gene_id":"ENSG00000273456.1","gene_symbol":"AC064836.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":202374932,"end":202375604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236305.1","gene_symbol":"SLC12A9-AS1","gene_name":"SLC12A9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40807]","synonyms":"RP11-126L15.4","biotype":"antisense_RNA","ncbi_id":"105375430","summary":null,"start":100837314,"end":100852616,"strand":-1,"description":"SLC12A9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40807]"}, {"versioned_ensembl_gene_id":"ENSG00000277804.4","gene_symbol":"PRTN3","gene_name":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]","synonyms":"PR-3,P29,MBT,C-ANCA,AGP7,ACPA","biotype":"protein_coding","ncbi_id":"5657","summary":null,"start":840960,"end":848175,"strand":1,"description":"proteinase 3 [Source:HGNC Symbol;Acc:HGNC:9495]"}, {"versioned_ensembl_gene_id":"ENSG00000090924.14","gene_symbol":"PLEKHG2","gene_name":"pleckstrin homology and RhoGEF domain containing G2 [Source:HGNC Symbol;Acc:HGNC:29515]","synonyms":"CLG,ARHGEF42,FLJ00018","biotype":"protein_coding","ncbi_id":"64857","summary":"The protein encoded by this gene is a RhoGTPase that can activate CDC42 by promoting exchange of GDP for GTP on CDC42. The encoded protein is activated by binding to the beta and gamma subunits of heterotrimeric guanine nucleotide-binding protein. Defects in this gene have been associated with leukodystrophy and acquired microcephaly with or without dystonia. [provided by RefSeq, May 2017]","start":39412585,"end":39428415,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G2 [Source:HGNC Symbol;Acc:HGNC:29515]"}, {"versioned_ensembl_gene_id":"ENSG00000282747.1","gene_symbol":"AC131056.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36326893,"end":36328453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151500.14","gene_symbol":"THYN1","gene_name":"thymocyte nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:29560]","synonyms":"THY28","biotype":"protein_coding","ncbi_id":"29087","summary":"This gene encodes a protein that is highly conserved among vertebrates and plant species and may be involved in the induction of apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":134248279,"end":134253370,"strand":-1,"description":"thymocyte nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:29560]"}, {"versioned_ensembl_gene_id":"ENSG00000197943.9","gene_symbol":"PLCG2","gene_name":"phospholipase C gamma 2 [Source:HGNC Symbol;Acc:HGNC:9066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5336","summary":"The protein encoded by this gene is a transmembrane signaling enzyme that catalyzes the conversion of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate to 1D-myo-inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) using calcium as a cofactor. IP3 and DAG are second messenger molecules important for transmitting signals from growth factor receptors and immune system receptors across the cell membrane. Mutations in this gene have been found in autoinflammation, antibody deficiency, and immune dysregulation syndrome and familial cold autoinflammatory syndrome 3. [provided by RefSeq, Mar 2014]","start":81739097,"end":81962693,"strand":1,"description":"phospholipase C gamma 2 [Source:HGNC Symbol;Acc:HGNC:9066]"}, {"versioned_ensembl_gene_id":"ENSG00000235713.1","gene_symbol":"AC004522.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99992397,"end":99993050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275358.1","gene_symbol":"AL080312.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25062962,"end":25063591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187151.7","gene_symbol":"ANGPTL5","gene_name":"angiopoietin like 5 [Source:HGNC Symbol;Acc:HGNC:19705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253935","summary":null,"start":101890674,"end":101916522,"strand":-1,"description":"angiopoietin like 5 [Source:HGNC Symbol;Acc:HGNC:19705]"}, {"versioned_ensembl_gene_id":"ENSG00000163743.13","gene_symbol":"RCHY1","gene_name":"ring finger and CHY zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17479]","synonyms":"ARNIP,ZNF363,ZCHY,RNF199,PRO1996,PIRH2,DKFZp586C1620,CHIMP","biotype":"protein_coding","ncbi_id":"25898","summary":"The protein encoded by this gene has ubiquitin ligase activity. It mediates E3-dependent ubiquitination and proteasomal degradation of target proteins, including tumor protein 53, histone deacetylase 1, and cyclin-dependent kinase inhibitor 1B, thus regulating their levels and cell cycle progression. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2013]","start":75479037,"end":75514764,"strand":-1,"description":"ring finger and CHY zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17479]"}, {"versioned_ensembl_gene_id":"ENSG00000203780.10","gene_symbol":"FANK1","gene_name":"fibronectin type III and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:23527]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92565","summary":null,"start":125896539,"end":126009592,"strand":1,"description":"fibronectin type III and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:23527]"}, {"versioned_ensembl_gene_id":"ENSG00000197177.15","gene_symbol":"ADGRA1","gene_name":"adhesion G protein-coupled receptor A1 [Source:HGNC Symbol;Acc:HGNC:13838]","synonyms":"KIAA1828,GPR123","biotype":"protein_coding","ncbi_id":"84435","summary":"This gene encodes a protein that belongs to the adhesion family of G-protein-coupled receptors. Members of this family function in several sensory systems and regulate blood pressure, immune responses, food intake and development. A similar protein in rodents is thought to play a role in in the regulation of neuronal signaling pathways. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Mar 2014]","start":133070929,"end":133131675,"strand":1,"description":"adhesion G protein-coupled receptor A1 [Source:HGNC Symbol;Acc:HGNC:13838]"}, {"versioned_ensembl_gene_id":"ENSG00000281365.1","gene_symbol":"AL049541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48471308,"end":48472414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225614.2","gene_symbol":"ZNF469","gene_name":"zinc finger protein 469 [Source:HGNC Symbol;Acc:HGNC:23216]","synonyms":"KIAA1858","biotype":"protein_coding","ncbi_id":"84627","summary":"This gene encodes a zinc-finger protein. Low-percent homology to certain collagens suggests that it may function as a transcription factor or extra-nuclear regulator factor for the synthesis or organization of collagen fibers. Mutations in this gene cause brittle cornea syndrome. [provided by RefSeq, Jul 2008]","start":88427471,"end":88440757,"strand":1,"description":"zinc finger protein 469 [Source:HGNC Symbol;Acc:HGNC:23216]"}, {"versioned_ensembl_gene_id":"ENSG00000236090.2","gene_symbol":"LDHAP3","gene_name":"lactate dehydrogenase A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:6538]","synonyms":"LDHAL3","biotype":"processed_pseudogene","ncbi_id":"442013","summary":null,"start":41819747,"end":41820754,"strand":1,"description":"lactate dehydrogenase A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:6538]"}, {"versioned_ensembl_gene_id":"ENSG00000233084.2","gene_symbol":"RPL23AP25","gene_name":"ribosomal protein L23a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35672]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653789","summary":null,"start":248936581,"end":248937043,"strand":1,"description":"ribosomal protein L23a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35672]"}, {"versioned_ensembl_gene_id":"ENSG00000166329.2","gene_symbol":"CCDC182","gene_name":"coiled-coil domain containing 182 [Source:HGNC Symbol;Acc:HGNC:49392]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101927581","summary":null,"start":57744481,"end":57745312,"strand":-1,"description":"coiled-coil domain containing 182 [Source:HGNC Symbol;Acc:HGNC:49392]"}, {"versioned_ensembl_gene_id":"ENSG00000154429.10","gene_symbol":"CCSAP","gene_name":"centriole, cilia and spindle associated protein [Source:HGNC Symbol;Acc:HGNC:29578]","synonyms":"CSAP,C1orf96,FLJ41471","biotype":"protein_coding","ncbi_id":"126731","summary":null,"start":229321005,"end":229343294,"strand":-1,"description":"centriole, cilia and spindle associated protein [Source:HGNC Symbol;Acc:HGNC:29578]"}, {"versioned_ensembl_gene_id":"ENSG00000234022.1","gene_symbol":"AC008278.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15564170,"end":15573868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226321.5","gene_symbol":"CROCC2","gene_name":"ciliary rootlet coiled-coil, rootletin family member 2 [Source:HGNC Symbol;Acc:HGNC:51677]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728763","summary":null,"start":240906330,"end":240993311,"strand":1,"description":"ciliary rootlet coiled-coil, rootletin family member 2 [Source:HGNC Symbol;Acc:HGNC:51677]"}, {"versioned_ensembl_gene_id":"ENSG00000258774.1","gene_symbol":"NANOGP7","gene_name":"Nanog homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23105]","synonyms":"NANOGP3","biotype":"transcribed_processed_pseudogene","ncbi_id":"414130","summary":null,"start":91604402,"end":91605319,"strand":-1,"description":"Nanog homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23105]"}, {"versioned_ensembl_gene_id":"ENSG00000283321.1","gene_symbol":"AC019117.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17299295,"end":17467234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091106.18","gene_symbol":"NLRC4","gene_name":"NLR family CARD domain containing 4 [Source:HGNC Symbol;Acc:HGNC:16412]","synonyms":"CLR2.1,CLAND,CLANC,CLANB,CLANA,CLAN1,CLAN,CARD12,ipaf","biotype":"protein_coding","ncbi_id":"58484","summary":"This gene encodes a member of the caspase recruitment domain-containing NLR family. Family members play essential roles in innate immune response to a wide range of pathogenic organisms, tissue damage and other cellular stresses. Mutations in this gene result in autoinflammation with infantile enterocolitis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":32224453,"end":32265854,"strand":-1,"description":"NLR family CARD domain containing 4 [Source:HGNC Symbol;Acc:HGNC:16412]"}, {"versioned_ensembl_gene_id":"ENSG00000102362.15","gene_symbol":"SYTL4","gene_name":"synaptotagmin like 4 [Source:HGNC Symbol;Acc:HGNC:15588]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94121","summary":"This gene encodes a member of the synaptotagmin like protein family. Members of this family are characterized by an N-terminal Rab27 binding domain and C-terminal tandem C2 domains. The encoded protein binds specific small Rab GTPases and is involved in intracellular membrane trafficking. This protein binds Rab27 and may be involved in inhibiting dense core vesicle exocytosis. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Mar 2010]","start":100674491,"end":100732123,"strand":-1,"description":"synaptotagmin like 4 [Source:HGNC Symbol;Acc:HGNC:15588]"}, {"versioned_ensembl_gene_id":"ENSG00000181885.18","gene_symbol":"CLDN7","gene_name":"claudin 7 [Source:HGNC Symbol;Acc:HGNC:2049]","synonyms":"Hs.84359,CPETRL2,CEPTRL2","biotype":"protein_coding","ncbi_id":"1366","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. Differential expression of this gene has been observed in different types of malignancies, including breast cancer, ovarian cancer, hepatocellular carcinomas, urinary tumors, prostate cancer, lung cancer, head and neck cancers, thyroid carcinomas, etc.. Alternatively spliced transcript variants encoding different isoforms have been found.[provided by RefSeq, May 2010]","start":7259903,"end":7263983,"strand":-1,"description":"claudin 7 [Source:HGNC Symbol;Acc:HGNC:2049]"}, {"versioned_ensembl_gene_id":"ENSG00000258474.1","gene_symbol":"LINC02313","gene_name":"long intergenic non-protein coding RNA 2313 [Source:HGNC Symbol;Acc:HGNC:53232]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370439","summary":null,"start":31944853,"end":31950382,"strand":1,"description":"long intergenic non-protein coding RNA 2313 [Source:HGNC Symbol;Acc:HGNC:53232]"}, {"versioned_ensembl_gene_id":"ENSG00000275002.1","gene_symbol":"AL352984.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31964550,"end":31965095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237626.1","gene_symbol":"AL161629.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89978282,"end":89987486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151338.18","gene_symbol":"MIPOL1","gene_name":"mirror-image polydactyly 1 [Source:HGNC Symbol;Acc:HGNC:21460]","synonyms":"CCDC193","biotype":"protein_coding","ncbi_id":"145282","summary":"This gene encodes a coiled-coil domain-containing protein. The encoded protein may function as a tumor suppressor. A translocation that results in truncation of the protein encoded by this locus has been associated with mirror-image polydactyly, also known as Laurin-Sandrow Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2010]","start":37197913,"end":37552361,"strand":1,"description":"mirror-image polydactyly 1 [Source:HGNC Symbol;Acc:HGNC:21460]"}, {"versioned_ensembl_gene_id":"ENSG00000176153.11","gene_symbol":"GPX2","gene_name":"glutathione peroxidase 2 [Source:HGNC Symbol;Acc:HGNC:4554]","synonyms":"GSHPX-GI","biotype":"protein_coding","ncbi_id":"2877","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is predominantly expressed in the gastrointestinal tract (also in liver in human), is localized in the cytoplasm, and whose preferred substrate is hydrogen peroxide. Overexpression of this gene is associated with increased differentiation and proliferation in colorectal cancer. This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2016]","start":64939152,"end":64942905,"strand":-1,"description":"glutathione peroxidase 2 [Source:HGNC Symbol;Acc:HGNC:4554]"}, {"versioned_ensembl_gene_id":"ENSG00000102081.13","gene_symbol":"FMR1","gene_name":"fragile X mental retardation 1 [Source:HGNC Symbol;Acc:HGNC:3775]","synonyms":"FMRP,POF1,POF,MGC87458,FRAXA","biotype":"protein_coding","ncbi_id":"2332","summary":"The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010]","start":147911951,"end":147951125,"strand":1,"description":"fragile X mental retardation 1 [Source:HGNC Symbol;Acc:HGNC:3775]"}, {"versioned_ensembl_gene_id":"ENSG00000224620.2","gene_symbol":"MEF2AP1","gene_name":"myocyte enhancer factor 2A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6994]","synonyms":"MEF2AP","biotype":"processed_pseudogene","ncbi_id":"4206","summary":null,"start":179447578,"end":179448440,"strand":-1,"description":"myocyte enhancer factor 2A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6994]"}, {"versioned_ensembl_gene_id":"ENSG00000140575.12","gene_symbol":"IQGAP1","gene_name":"IQ motif containing GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:6110]","synonyms":"p195,KIAA0051,HUMORFA01,SAR1","biotype":"protein_coding","ncbi_id":"8826","summary":"This gene encodes a member of the IQGAP family. The protein contains four IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. It interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. Expression of the protein is upregulated by gene amplification in two gastric cancer cell lines. [provided by RefSeq, Jul 2008]","start":90388218,"end":90502243,"strand":1,"description":"IQ motif containing GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:6110]"}, {"versioned_ensembl_gene_id":"ENSG00000259177.1","gene_symbol":"AC018946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90393490,"end":90397881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253851.1","gene_symbol":"AC025370.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103228425,"end":103229314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236939.2","gene_symbol":"BAALC-AS2","gene_name":"BAALC antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:28595]","synonyms":"MGC39526,C8orf56,BAALCOS","biotype":"antisense_RNA","ncbi_id":"157556","summary":null,"start":103132963,"end":103141475,"strand":-1,"description":"BAALC antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:28595]"}, {"versioned_ensembl_gene_id":"ENSG00000174514.12","gene_symbol":"MFSD4A","gene_name":"major facilitator superfamily domain containing 4A [Source:HGNC Symbol;Acc:HGNC:25433]","synonyms":"UNQ3064,MFSD4,FLJ34577,FLJ25004,DKFZp761N1114","biotype":"protein_coding","ncbi_id":"148808","summary":null,"start":205568885,"end":205602918,"strand":1,"description":"major facilitator superfamily domain containing 4A [Source:HGNC Symbol;Acc:HGNC:25433]"}, {"versioned_ensembl_gene_id":"ENSG00000236942.1","gene_symbol":"AC096533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205625483,"end":205626153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196159.11","gene_symbol":"FAT4","gene_name":"FAT atypical cadherin 4 [Source:HGNC Symbol;Acc:HGNC:23109]","synonyms":"FAT-J,CDHR11,CDHF14","biotype":"protein_coding","ncbi_id":"79633","summary":"The protein encoded by this gene is a member of the protocadherin family. This gene may play a role in regulating planar cell polarity (PCP). Studies in mice suggest that loss of PCP signaling may cause cystic kidney disease, and mutations in this gene have been associated with Van Maldergem Syndrome 2. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Mar 2014]","start":125316399,"end":125492932,"strand":1,"description":"FAT atypical cadherin 4 [Source:HGNC Symbol;Acc:HGNC:23109]"}, {"versioned_ensembl_gene_id":"ENSG00000117697.14","gene_symbol":"NSL1","gene_name":"NSL1, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24548]","synonyms":"MIS14,DKFZP566O1646,DC8,C1orf48","biotype":"protein_coding","ncbi_id":"25936","summary":"This gene encodes a protein with two coiled-coil domains that localizes to kinetochores, which are chromosome-associated structures that attach to microtubules and mediate chromosome movements during cell division. The encoded protein is part of a conserved protein complex that includes two chromodomain-containing proteins and a component of the outer plate of the kinetochore. This protein complex is proposed to bridge centromeric heterochromatin with the outer kinetochore structure. Multiple transcript variants encoding different isoforms have been found for this gene. There is a pseudogene of the 3' UTR region of this gene on chromosome X. [provided by RefSeq, Jul 2014]","start":212726153,"end":212791782,"strand":-1,"description":"NSL1, MIS12 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24548]"}, {"versioned_ensembl_gene_id":"ENSG00000248565.2","gene_symbol":"TECRP2","gene_name":"trans-2,3-enoyl-CoA reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391696","summary":null,"start":124462863,"end":124463790,"strand":-1,"description":"trans-2,3-enoyl-CoA reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44051]"}, {"versioned_ensembl_gene_id":"ENSG00000254253.1","gene_symbol":"AC022861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67569416,"end":67570078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154153.13","gene_symbol":"RETREG1","gene_name":"reticulophagy regulator 1 [Source:HGNC Symbol;Acc:HGNC:25964]","synonyms":"JK1,FLJ20152,FAM134B","biotype":"protein_coding","ncbi_id":"54463","summary":"The protein encoded by this gene is a cis-Golgi transmembrane protein that may be necessary for the long-term survival of nociceptive and autonomic ganglion neurons. Mutations in this gene are a cause of hereditary sensory and autonomic neuropathy type IIB (HSAN IIB), and this gene may also play a role in susceptibility to vascular dementia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":16473038,"end":16617058,"strand":-1,"description":"reticulophagy regulator 1 [Source:HGNC Symbol;Acc:HGNC:25964]"}, {"versioned_ensembl_gene_id":"ENSG00000233689.1","gene_symbol":"AC104688.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69040152,"end":69046803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173960.13","gene_symbol":"UBXN2A","gene_name":"UBX domain protein 2A [Source:HGNC Symbol;Acc:HGNC:27265]","synonyms":"UBXD4","biotype":"protein_coding","ncbi_id":"165324","summary":null,"start":23927285,"end":24004909,"strand":1,"description":"UBX domain protein 2A [Source:HGNC Symbol;Acc:HGNC:27265]"}, {"versioned_ensembl_gene_id":"ENSG00000166913.12","gene_symbol":"YWHAB","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta [Source:HGNC Symbol;Acc:HGNC:12849]","synonyms":"YWHAA","biotype":"protein_coding","ncbi_id":"7529","summary":"This gene encodes a protein belonging to the 14-3-3 family of proteins, members of which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals. The encoded protein has been shown to interact with RAF1 and CDC25 phosphatases, suggesting that it may play a role in linking mitogenic signaling and the cell cycle machinery. Two transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":44885676,"end":44908532,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta [Source:HGNC Symbol;Acc:HGNC:12849]"}, {"versioned_ensembl_gene_id":"ENSG00000258214.1","gene_symbol":"AC108721.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59366218,"end":59411171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228928.1","gene_symbol":"KPNA2P2","gene_name":"karyopherin subunit alpha 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52872]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645680","summary":null,"start":88564793,"end":88566281,"strand":-1,"description":"karyopherin subunit alpha 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52872]"}, {"versioned_ensembl_gene_id":"ENSG00000173545.4","gene_symbol":"ZNF622","gene_name":"zinc finger protein 622 [Source:HGNC Symbol;Acc:HGNC:30958]","synonyms":"ZPR9,MGC2485,MGC17552","biotype":"protein_coding","ncbi_id":"90441","summary":null,"start":16451519,"end":16465792,"strand":-1,"description":"zinc finger protein 622 [Source:HGNC Symbol;Acc:HGNC:30958]"}, {"versioned_ensembl_gene_id":"ENSG00000198054.11","gene_symbol":"DSCR8","gene_name":"Down syndrome critical region 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16707]","synonyms":"MTAG2,MMA-1b,MMA-1a,CT25.1b,CT25.1a,C21orf65","biotype":"protein_coding","ncbi_id":"84677","summary":null,"start":38121451,"end":38188016,"strand":1,"description":"Down syndrome critical region 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16707]"}, {"versioned_ensembl_gene_id":"ENSG00000233316.4","gene_symbol":"DSCR10","gene_name":"Down syndrome critical region 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16302]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"259234","summary":null,"start":38206156,"end":38208644,"strand":1,"description":"Down syndrome critical region 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16302]"}, {"versioned_ensembl_gene_id":"ENSG00000230099.2","gene_symbol":"TRBV5-4","gene_name":"T-cell receptor beta variable 5-4 [Source:HGNC Symbol;Acc:HGNC:12221]","synonyms":"TCRBV5S6A3N2T,TCRBV5S4,TRBV54","biotype":"TR_V_gene","ncbi_id":"28611","summary":null,"start":142462916,"end":142463581,"strand":1,"description":"T-cell receptor beta variable 5-4 [Source:HGNC Symbol;Acc:HGNC:12221]"}, {"versioned_ensembl_gene_id":"ENSG00000251126.2","gene_symbol":"AC017007.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112880298,"end":112882330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149571.11","gene_symbol":"KIRREL3","gene_name":"kirre like nephrin family adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:23204]","synonyms":"KIRRE,KIAA1867,NEPH2","biotype":"protein_coding","ncbi_id":"84623","summary":"The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":126423359,"end":127003460,"strand":-1,"description":"kirre like nephrin family adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:23204]"}, {"versioned_ensembl_gene_id":"ENSG00000249367.1","gene_symbol":"FABP5P12","gene_name":"fatty acid binding protein 5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:31067]","synonyms":"FABP5L12","biotype":"processed_pseudogene","ncbi_id":"100270673","summary":null,"start":159026139,"end":159026527,"strand":1,"description":"fatty acid binding protein 5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:31067]"}, {"versioned_ensembl_gene_id":"ENSG00000231963.1","gene_symbol":"AL662864.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73080167,"end":73084635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261411.1","gene_symbol":"AL161938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11685144,"end":11687323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125821.11","gene_symbol":"DTD1","gene_name":"D-tyrosyl-tRNA deacylase 1 [Source:HGNC Symbol;Acc:HGNC:16219]","synonyms":"bA555E18.1,bA379J5.3,pqn-68,MGC41905,MGC119131,HARS2,DUEB,C20orf88","biotype":"protein_coding","ncbi_id":"92675","summary":"The protein encoded by this gene is similar in sequence to histidyl-tRNA synthetase, which hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). The encoded protein binds the DNA unwinding element and plays a role in the initiation of DNA replication. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":18567453,"end":18763917,"strand":1,"description":"D-tyrosyl-tRNA deacylase 1 [Source:HGNC Symbol;Acc:HGNC:16219]"}, {"versioned_ensembl_gene_id":"ENSG00000225999.1","gene_symbol":"NDUFA12P1","gene_name":"NADH:ubiquinone oxidoreductase subunit A12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39419]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100527945","summary":null,"start":100027769,"end":100028174,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39419]"}, {"versioned_ensembl_gene_id":"ENSG00000260738.1","gene_symbol":"LINC00554","gene_name":"long intergenic non-protein coding RNA 554 [Source:HGNC Symbol;Acc:HGNC:43697]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861542","summary":null,"start":99994899,"end":99997909,"strand":-1,"description":"long intergenic non-protein coding RNA 554 [Source:HGNC Symbol;Acc:HGNC:43697]"}, {"versioned_ensembl_gene_id":"ENSG00000204524.6","gene_symbol":"ZNF805","gene_name":"zinc finger protein 805 [Source:HGNC Symbol;Acc:HGNC:23272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390980","summary":null,"start":57240685,"end":57255135,"strand":1,"description":"zinc finger protein 805 [Source:HGNC Symbol;Acc:HGNC:23272]"}, {"versioned_ensembl_gene_id":"ENSG00000105251.10","gene_symbol":"SHD","gene_name":"Src homology 2 domain containing transforming protein D [Source:HGNC Symbol;Acc:HGNC:30633]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56961","summary":null,"start":4278601,"end":4290724,"strand":1,"description":"Src homology 2 domain containing transforming protein D [Source:HGNC Symbol;Acc:HGNC:30633]"}, {"versioned_ensembl_gene_id":"ENSG00000151503.12","gene_symbol":"NCAPD3","gene_name":"non-SMC condensin II complex subunit D3 [Source:HGNC Symbol;Acc:HGNC:28952]","synonyms":"KIAA0056,hHCP-6,hcp-6,hCAP-D3,FLJ42888,CAP-D3","biotype":"protein_coding","ncbi_id":"23310","summary":"Condensin complexes I and II play essential roles in mitotic chromosome assembly and segregation. Both condensins contain 2 invariant structural maintenance of chromosome (SMC) subunits, SMC2 (MIM 605576) and SMC4 (MIM 605575), but they contain different sets of non-SMC subunits. NCAPD3 is 1 of 3 non-SMC subunits that define condensin II (Ono et al., 2003 [PubMed 14532007]).[supplied by OMIM, Mar 2008]","start":134150119,"end":134225454,"strand":-1,"description":"non-SMC condensin II complex subunit D3 [Source:HGNC Symbol;Acc:HGNC:28952]"}, {"versioned_ensembl_gene_id":"ENSG00000241657.1","gene_symbol":"TRBV11-2","gene_name":"T-cell receptor beta variable 11-2 [Source:HGNC Symbol;Acc:HGNC:12181]","synonyms":"TRBV112,TCRBV21S3A2N2T,TCRBV11S2","biotype":"lincRNA","ncbi_id":"28581","summary":null,"start":142433895,"end":142434394,"strand":1,"description":"T-cell receptor beta variable 11-2 [Source:HGNC Symbol;Acc:HGNC:12181]"}, {"versioned_ensembl_gene_id":"ENSG00000152683.14","gene_symbol":"SLC30A6","gene_name":"solute carrier family 30 member 6 [Source:HGNC Symbol;Acc:HGNC:19305]","synonyms":"ZNT6,FLJ31101","biotype":"protein_coding","ncbi_id":"55676","summary":"This gene encodes a member of a family of proteins that function as zinc transporters. This protein can regulate subcellular levels of zinc in the Golgi and vesicles. Expression of this gene is altered in the Alzheimer's disease brain plaques. [provided by RefSeq, Aug 2016]","start":32165841,"end":32224379,"strand":1,"description":"solute carrier family 30 member 6 [Source:HGNC Symbol;Acc:HGNC:19305]"}, {"versioned_ensembl_gene_id":"ENSG00000183929.7","gene_symbol":"DUSP5P1","gene_name":"dual specificity phosphatase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32020]","synonyms":"FLJ34941,DUSP5P","biotype":"processed_pseudogene","ncbi_id":"574029","summary":null,"start":228650241,"end":228651379,"strand":1,"description":"dual specificity phosphatase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32020]"}, {"versioned_ensembl_gene_id":"ENSG00000280295.1","gene_symbol":"AC099811.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":42233832,"end":42235469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277655.1","gene_symbol":"AC245407.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":146459449,"end":146461859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011451.17","gene_symbol":"WIZ","gene_name":"widely interspaced zinc finger motifs [Source:HGNC Symbol;Acc:HGNC:30917]","synonyms":"ZNF803","biotype":"protein_coding","ncbi_id":"58525","summary":null,"start":15419980,"end":15449951,"strand":-1,"description":"widely interspaced zinc finger motifs [Source:HGNC Symbol;Acc:HGNC:30917]"}, {"versioned_ensembl_gene_id":"ENSG00000261680.1","gene_symbol":"AC093249.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30624285,"end":30624714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242152.1","gene_symbol":"AC108729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155431229,"end":155433398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007350.16","gene_symbol":"TKTL1","gene_name":"transketolase like 1 [Source:HGNC Symbol;Acc:HGNC:11835]","synonyms":"TKT2,TKR","biotype":"protein_coding","ncbi_id":"8277","summary":"The protein encoded by this gene is a transketolase that acts as a homodimer and catalyzes the conversion of sedoheptulose 7-phosphate and D-glyceraldehyde 3-phosphate to D-ribose 5-phosphate and D-xylulose 5-phosphate. This reaction links the pentose phosphate pathway with the glycolytic pathway. Variations in this gene may be the cause of Wernicke-Korsakoff syndrome. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":154295671,"end":154330350,"strand":1,"description":"transketolase like 1 [Source:HGNC Symbol;Acc:HGNC:11835]"}, {"versioned_ensembl_gene_id":"ENSG00000105701.15","gene_symbol":"FKBP8","gene_name":"FK506 binding protein 8 [Source:HGNC Symbol;Acc:HGNC:3724]","synonyms":"FKBPr38,FKBP38","biotype":"protein_coding","ncbi_id":"23770","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. Unlike the other members of the family, this encoded protein does not seem to have PPIase/rotamase activity. It may have a role in neurons associated with memory function. [provided by RefSeq, Jul 2008]","start":18531751,"end":18544077,"strand":-1,"description":"FK506 binding protein 8 [Source:HGNC Symbol;Acc:HGNC:3724]"}, {"versioned_ensembl_gene_id":"ENSG00000119771.14","gene_symbol":"KLHL29","gene_name":"kelch like family member 29 [Source:HGNC Symbol;Acc:HGNC:29404]","synonyms":"KIAA1921,KBTBD9","biotype":"protein_coding","ncbi_id":"114818","summary":null,"start":23385217,"end":23708611,"strand":1,"description":"kelch like family member 29 [Source:HGNC Symbol;Acc:HGNC:29404]"}, {"versioned_ensembl_gene_id":"ENSG00000178462.11","gene_symbol":"TUBAL3","gene_name":"tubulin alpha like 3 [Source:HGNC Symbol;Acc:HGNC:23534]","synonyms":"FLJ21665","biotype":"protein_coding","ncbi_id":"79861","summary":null,"start":5393098,"end":5404830,"strand":-1,"description":"tubulin alpha like 3 [Source:HGNC Symbol;Acc:HGNC:23534]"}, {"versioned_ensembl_gene_id":"ENSG00000076351.12","gene_symbol":"SLC46A1","gene_name":"solute carrier family 46 member 1 [Source:HGNC Symbol;Acc:HGNC:30521]","synonyms":"PCFT,MGC9564,HCP1","biotype":"protein_coding","ncbi_id":"113235","summary":"This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]","start":28394756,"end":28407197,"strand":-1,"description":"solute carrier family 46 member 1 [Source:HGNC Symbol;Acc:HGNC:30521]"}, {"versioned_ensembl_gene_id":"ENSG00000231591.6","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32997846,"end":33000255,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000280450.1","gene_symbol":"AL683826.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":5346651,"end":5347277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165983.14","gene_symbol":"PTER","gene_name":"phosphotriesterase related [Source:HGNC Symbol;Acc:HGNC:9590]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9317","summary":null,"start":16436943,"end":16513745,"strand":1,"description":"phosphotriesterase related [Source:HGNC Symbol;Acc:HGNC:9590]"}, {"versioned_ensembl_gene_id":"ENSG00000254100.1","gene_symbol":"AC069120.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38552248,"end":38559020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226173.4","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32998969,"end":33007738,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000284607.1","gene_symbol":"AL121936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26569324,"end":26574698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279189.1","gene_symbol":"AP003972.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133297189,"end":133302634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275959.1","gene_symbol":"AC108467.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44994426,"end":44996022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280169.1","gene_symbol":"AL136526.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100537365,"end":100539567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225594.1","gene_symbol":"AC098826.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":132087289,"end":132102564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237710.10","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33053864,"end":33065131,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000214226.8","gene_symbol":"C17orf67","gene_name":"chromosome 17 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:27900]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339210","summary":null,"start":56791913,"end":56838773,"strand":-1,"description":"chromosome 17 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:27900]"}, {"versioned_ensembl_gene_id":"ENSG00000258169.1","gene_symbol":"LINC00485","gene_name":"long intergenic non-protein coding RNA 485 [Source:HGNC Symbol;Acc:HGNC:27476]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283432","summary":null,"start":102809280,"end":102824399,"strand":-1,"description":"long intergenic non-protein coding RNA 485 [Source:HGNC Symbol;Acc:HGNC:27476]"}, {"versioned_ensembl_gene_id":"ENSG00000228980.3","gene_symbol":"LINC01205","gene_name":"long intergenic non-protein coding RNA 1205 [Source:HGNC Symbol;Acc:HGNC:49636]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401082","summary":null,"start":109409990,"end":109495167,"strand":1,"description":"long intergenic non-protein coding RNA 1205 [Source:HGNC Symbol;Acc:HGNC:49636]"}, {"versioned_ensembl_gene_id":"ENSG00000152117.17","gene_symbol":"AC073869.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":131492813,"end":131521573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109321.10","gene_symbol":"AREG","gene_name":"amphiregulin [Source:HGNC Symbol;Acc:HGNC:651]","synonyms":"SDGF,AREGB","biotype":"protein_coding","ncbi_id":"374","summary":"The protein encoded by this gene is a member of the epidermal growth factor family. It is an autocrine growth factor as well as a mitogen for astrocytes, Schwann cells and fibroblasts. It is related to epidermal growth factor (EGF) and transforming growth factor alpha (TGF-alpha). The protein interacts with the EGF/TGF-alpha receptor to promote the growth of normal epithelial cells, and it inhibits the growth of certain aggressive carcinoma cell lines. It also functions in mammary gland, oocyte and bone tissue development. This gene is associated with a psoriasis-like skin phenotype, and is also associated with other pathological disorders, including various types of cancers and inflammatory conditions. [provided by RefSeq, Apr 2014]","start":74445134,"end":74455009,"strand":1,"description":"amphiregulin [Source:HGNC Symbol;Acc:HGNC:651]"}, {"versioned_ensembl_gene_id":"ENSG00000261156.6","gene_symbol":"LINC01989","gene_name":"long intergenic non-protein coding RNA 1989 [Source:HGNC Symbol;Acc:HGNC:52821]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927239","summary":null,"start":34169372,"end":34195937,"strand":-1,"description":"long intergenic non-protein coding RNA 1989 [Source:HGNC Symbol;Acc:HGNC:52821]"}, {"versioned_ensembl_gene_id":"ENSG00000265179.6","gene_symbol":"AP000894.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":902766,"end":906667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279416.1","gene_symbol":"AC099689.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79085134,"end":79086435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197405.7","gene_symbol":"C5AR1","gene_name":"complement C5a receptor 1 [Source:HGNC Symbol;Acc:HGNC:1338]","synonyms":"CD88,C5R1,C5AR,C5A","biotype":"protein_coding","ncbi_id":"728","summary":null,"start":47290023,"end":47322066,"strand":1,"description":"complement C5a receptor 1 [Source:HGNC Symbol;Acc:HGNC:1338]"}, {"versioned_ensembl_gene_id":"ENSG00000267655.1","gene_symbol":"AC125437.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79117207,"end":79117920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271347.1","gene_symbol":"AC124312.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24991486,"end":24991753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154122.12","gene_symbol":"ANKH","gene_name":"ANKH inorganic pyrophosphate transport regulator [Source:HGNC Symbol;Acc:HGNC:15492]","synonyms":"HANK,CPPDD,CMDJ,CCAL2,ANK","biotype":"protein_coding","ncbi_id":"56172","summary":"This gene encodes a multipass transmembrane protein that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. Progressive ankylosis-mediated control of pyrophosphate levels has been suggested as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals. Mutations in this gene have been associated with autosomal dominant craniometaphyseal dysplasia. [provided by RefSeq, Jul 2008]","start":14704804,"end":14871778,"strand":-1,"description":"ANKH inorganic pyrophosphate transport regulator [Source:HGNC Symbol;Acc:HGNC:15492]"}, {"versioned_ensembl_gene_id":"ENSG00000236832.1","gene_symbol":"AC073465.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173477996,"end":173478400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233594.2","gene_symbol":"BTF3P5","gene_name":"basic transcription factor 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652959","summary":null,"start":55435156,"end":55435622,"strand":-1,"description":"basic transcription factor 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38565]"}, {"versioned_ensembl_gene_id":"ENSG00000223868.1","gene_symbol":"AL845458.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31192602,"end":31194361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273888.1","gene_symbol":"FRMD6-AS1","gene_name":"FRMD6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20129]","synonyms":"C14orf82","biotype":"antisense_RNA","ncbi_id":"145438","summary":null,"start":51649516,"end":51651744,"strand":-1,"description":"FRMD6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20129]"}, {"versioned_ensembl_gene_id":"ENSG00000223971.1","gene_symbol":"AL669854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31367866,"end":31368468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282821.1","gene_symbol":"IGHV3-65","gene_name":"immunoglobulin heavy variable 3-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5618]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28413","summary":null,"start":106690773,"end":106691213,"strand":-1,"description":"immunoglobulin heavy variable 3-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5618]"}, {"versioned_ensembl_gene_id":"ENSG00000282082.1","gene_symbol":"IGHVII-60-1","gene_name":"immunoglobulin heavy variable (II)-60-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5686]","synonyms":"IGHV(II)-60-1","biotype":"IG_V_pseudogene","ncbi_id":"28361","summary":null,"start":106662399,"end":106662654,"strand":-1,"description":"immunoglobulin heavy variable (II)-60-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5686]"}, {"versioned_ensembl_gene_id":"ENSG00000272442.2","gene_symbol":"AL353588.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":44273194,"end":44378957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176083.17","gene_symbol":"ZNF683","gene_name":"zinc finger protein 683 [Source:HGNC Symbol;Acc:HGNC:28495]","synonyms":"MGC33414,Hobit","biotype":"protein_coding","ncbi_id":"257101","summary":null,"start":26361634,"end":26374522,"strand":-1,"description":"zinc finger protein 683 [Source:HGNC Symbol;Acc:HGNC:28495]"}, {"versioned_ensembl_gene_id":"ENSG00000249973.2","gene_symbol":"CHCHD2P7","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39591]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874509","summary":null,"start":87785920,"end":87786371,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39591]"}, {"versioned_ensembl_gene_id":"ENSG00000260621.1","gene_symbol":"AC092140.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56409320,"end":56411683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153815.16","gene_symbol":"CMIP","gene_name":"c-Maf inducing protein [Source:HGNC Symbol;Acc:HGNC:24319]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80790","summary":"This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":81445170,"end":81711762,"strand":1,"description":"c-Maf inducing protein [Source:HGNC Symbol;Acc:HGNC:24319]"}, {"versioned_ensembl_gene_id":"ENSG00000273032.1","gene_symbol":"DGCR9","gene_name":"DiGeorge syndrome critical region gene 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17227]","synonyms":"POM121L5P,DGS-A","biotype":"lincRNA","ncbi_id":"25787","summary":null,"start":19017834,"end":19020248,"strand":1,"description":"DiGeorge syndrome critical region gene 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17227]"}, {"versioned_ensembl_gene_id":"ENSG00000163702.18","gene_symbol":"IL17RC","gene_name":"interleukin 17 receptor C [Source:HGNC Symbol;Acc:HGNC:18358]","synonyms":"IL17-RL","biotype":"protein_coding","ncbi_id":"84818","summary":"This gene encodes a single-pass type I membrane protein that shares similarity with the interleukin-17 receptor (IL-17RA). Unlike IL-17RA, which is predominantly expressed in hemopoietic cells, and binds with high affinity to only IL-17A, this protein is expressed in nonhemopoietic tissues, and binds both IL-17A and IL-17F with similar affinities. The proinflammatory cytokines, IL-17A and IL-17F, have been implicated in the progression of inflammatory and autoimmune diseases. Multiple alternatively spliced transcript variants encoding different isoforms have been detected for this gene, and it has been proposed that soluble, secreted proteins lacking transmembrane and intracellular domains may function as extracellular antagonists to cytokine signaling. [provided by RefSeq, Feb 2011]","start":9917074,"end":9933630,"strand":1,"description":"interleukin 17 receptor C [Source:HGNC Symbol;Acc:HGNC:18358]"}, {"versioned_ensembl_gene_id":"ENSG00000283583.1","gene_symbol":"AC007326.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18980695,"end":18981325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100109.16","gene_symbol":"TFIP11","gene_name":"tuftelin interacting protein 11 [Source:HGNC Symbol;Acc:HGNC:17165]","synonyms":"Spp382,DKFZP434B194,TIP39","biotype":"protein_coding","ncbi_id":"24144","summary":"This gene encodes a protein component of the spliceosome that promotes the release of the lariat-intron during late-stage splicing through the recruitment of a pre-mRNA splicing factor called DEAH-box helicase 15. The encoded protein contains a G-patch domain, a hallmark of RNA-processing proteins, that binds DEAH-box helicase 15. This protein contains an atypical nuclear localization sequence as well as a nuclear speckle-targeting sequence, enabling it to localize to distinct speckled regions within the cell nucleus. Polymorphisms in this gene are associated with dental caries suggesting a role in amelogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":26491225,"end":26512505,"strand":-1,"description":"tuftelin interacting protein 11 [Source:HGNC Symbol;Acc:HGNC:17165]"}, {"versioned_ensembl_gene_id":"ENSG00000169957.9","gene_symbol":"ZNF768","gene_name":"zinc finger protein 768 [Source:HGNC Symbol;Acc:HGNC:26273]","synonyms":"FLJ23436","biotype":"protein_coding","ncbi_id":"79724","summary":null,"start":30524001,"end":30526821,"strand":-1,"description":"zinc finger protein 768 [Source:HGNC Symbol;Acc:HGNC:26273]"}, {"versioned_ensembl_gene_id":"ENSG00000233383.1","gene_symbol":"AC073089.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67089257,"end":67089470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164113.10","gene_symbol":"ADAD1","gene_name":"adenosine deaminase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30713]","synonyms":"Tenr","biotype":"protein_coding","ncbi_id":"132612","summary":null,"start":122378966,"end":122429802,"strand":1,"description":"adenosine deaminase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30713]"}, {"versioned_ensembl_gene_id":"ENSG00000157540.19","gene_symbol":"DYRK1A","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 1A [Source:HGNC Symbol;Acc:HGNC:3091]","synonyms":"MNBH,DYRK1,DYRK","biotype":"protein_coding","ncbi_id":"1859","summary":"This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5' UTR or in the 3' coding region. These variants encode at least five different isoforms. [provided by RefSeq, Jul 2008]","start":37365790,"end":37517450,"strand":1,"description":"dual specificity tyrosine phosphorylation regulated kinase 1A [Source:HGNC Symbol;Acc:HGNC:3091]"}, {"versioned_ensembl_gene_id":"ENSG00000220008.3","gene_symbol":"LINGO3","gene_name":"leucine rich repeat and Ig domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21206]","synonyms":"LRRN6B,LERN2","biotype":"protein_coding","ncbi_id":"645191","summary":null,"start":2289784,"end":2292024,"strand":-1,"description":"leucine rich repeat and Ig domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21206]"}, {"versioned_ensembl_gene_id":"ENSG00000145087.12","gene_symbol":"STXBP5L","gene_name":"syntaxin binding protein 5 like [Source:HGNC Symbol;Acc:HGNC:30757]","synonyms":"LLGL4,KIAA1006","biotype":"protein_coding","ncbi_id":"9515","summary":"The protein encoded by this gene is similar to syntaxin-binding protein 5 and contains ten N-terminal WD40 repeats, four variable region WD40 repeats, and a C-terminal R-SNARE domain. Studies of the orthologous proteins in mouse and rat have shown that the encoded protein may inhibit exocytosis in neurosecretory cells, and may negatively regulate the secretion of insulin. A missense variant in this gene is likely the cause of an infantile-onset neurodegenerative disorder diagnosed in two siblings of consanguineous parents. [provided by RefSeq, Jan 2017]","start":120908072,"end":121424761,"strand":1,"description":"syntaxin binding protein 5 like [Source:HGNC Symbol;Acc:HGNC:30757]"}, {"versioned_ensembl_gene_id":"ENSG00000254694.1","gene_symbol":"AP001893.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126208611,"end":126209027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260495.1","gene_symbol":"AC009148.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81310731,"end":81313423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270782.1","gene_symbol":"AC072026.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120924612,"end":120925158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005187.11","gene_symbol":"ACSM3","gene_name":"acyl-CoA synthetase medium chain family member 3 [Source:HGNC Symbol;Acc:HGNC:10522]","synonyms":"SAH,SA","biotype":"protein_coding","ncbi_id":"6296","summary":null,"start":20610243,"end":20797581,"strand":1,"description":"acyl-CoA synthetase medium chain family member 3 [Source:HGNC Symbol;Acc:HGNC:10522]"}, {"versioned_ensembl_gene_id":"ENSG00000273522.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR2DL6,KIRY,KIRZ,KIR15","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755023,"end":54767371,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000137075.17","gene_symbol":"RNF38","gene_name":"ring finger protein 38 [Source:HGNC Symbol;Acc:HGNC:18052]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152006","summary":"This gene encodes a protein with a coiled-coil motif and a RING-H2 motif (C3H2C2) at its carboxy-terminus. The RING motif is a zinc-binding domain found in a large set of proteins playing roles in diverse cellular processes including oncogenesis, development, signal transduction, and apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":36336396,"end":36487548,"strand":-1,"description":"ring finger protein 38 [Source:HGNC Symbol;Acc:HGNC:18052]"}, {"versioned_ensembl_gene_id":"ENSG00000123358.19","gene_symbol":"NR4A1","gene_name":"nuclear receptor subfamily 4 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7980]","synonyms":"TR3,NUR77,NGFIB,NAK-1,N10,HMR,GFRP1","biotype":"protein_coding","ncbi_id":"3164","summary":"This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. Expression is induced by phytohemagglutinin in human lymphocytes and by serum stimulation of arrested fibroblasts. The encoded protein acts as a nuclear transcription factor. Translocation of the protein from the nucleus to mitochondria induces apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":52022832,"end":52059507,"strand":1,"description":"nuclear receptor subfamily 4 group A member 1 [Source:HGNC Symbol;Acc:HGNC:7980]"}, {"versioned_ensembl_gene_id":"ENSG00000270571.2","gene_symbol":"AC007681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75154366,"end":75189949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261904.1","gene_symbol":"MTND5P33","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:51952]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075118","summary":null,"start":10720015,"end":10721464,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:51952]"}, {"versioned_ensembl_gene_id":"ENSG00000254292.1","gene_symbol":"IGKV2D-14","gene_name":"immunoglobulin kappa variable 2D-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5793]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28889","summary":null,"start":90121786,"end":90122564,"strand":1,"description":"immunoglobulin kappa variable 2D-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5793]"}, {"versioned_ensembl_gene_id":"ENSG00000235136.1","gene_symbol":"AL627224.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55599663,"end":55600106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176092.14","gene_symbol":"CRYBG2","gene_name":"crystallin beta-gamma domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17295]","synonyms":"FLJ38020,AIM1L","biotype":"protein_coding","ncbi_id":"55057","summary":null,"start":26321859,"end":26360052,"strand":-1,"description":"crystallin beta-gamma domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17295]"}, {"versioned_ensembl_gene_id":"ENSG00000236638.1","gene_symbol":"AC006455.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63263065,"end":63263456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164023.14","gene_symbol":"SGMS2","gene_name":"sphingomyelin synthase 2 [Source:HGNC Symbol;Acc:HGNC:28395]","synonyms":"SMS2,MGC26963","biotype":"protein_coding","ncbi_id":"166929","summary":"Sphingomyelin, a major component of cell and Golgi membranes, is made by the transfer of phosphocholine from phosphatidylcholine onto ceramide, with diacylglycerol as a side product. The protein encoded by this gene is an enzyme that catalyzes this reaction primarily at the cell membrane. The synthesis is reversible, and this enzyme can catalyze the reaction in either direction. The encoded protein is required for cell growth. Three transcript variants encoding the same protein have been found for this gene. There is evidence for more variants, but the full-length nature of their transcripts has not been determined.[provided by RefSeq, Oct 2008]","start":107824563,"end":107915047,"strand":1,"description":"sphingomyelin synthase 2 [Source:HGNC Symbol;Acc:HGNC:28395]"}, {"versioned_ensembl_gene_id":"ENSG00000241423.2","gene_symbol":"RPL21P103","gene_name":"ribosomal protein L21 pseudogene 103 [Source:HGNC Symbol;Acc:HGNC:36732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271433","summary":null,"start":58244378,"end":58244865,"strand":1,"description":"ribosomal protein L21 pseudogene 103 [Source:HGNC Symbol;Acc:HGNC:36732]"}, {"versioned_ensembl_gene_id":"ENSG00000172725.13","gene_symbol":"CORO1B","gene_name":"coronin 1B [Source:HGNC Symbol;Acc:HGNC:2253]","synonyms":"coronin-2","biotype":"protein_coding","ncbi_id":"57175","summary":"Members of the coronin family, such as CORO1B, are WD repeat-containing actin-binding proteins that regulate cell motility (Cai et al., 2005 [PubMed 16027158]).[supplied by OMIM, Mar 2008]","start":67435510,"end":67443821,"strand":-1,"description":"coronin 1B [Source:HGNC Symbol;Acc:HGNC:2253]"}, {"versioned_ensembl_gene_id":"ENSG00000224463.1","gene_symbol":"AC079354.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202231696,"end":202231849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250321.1","gene_symbol":"AC079140.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":342821,"end":342962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249492.1","gene_symbol":"AC114956.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":43483959,"end":43509356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230618.3","gene_symbol":"H3F3AP3","gene_name":"H3 histone family member 3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42873]","synonyms":"p18","biotype":"processed_pseudogene","ncbi_id":"100689229","summary":null,"start":109409678,"end":109410084,"strand":-1,"description":"H3 histone family member 3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42873]"}, {"versioned_ensembl_gene_id":"ENSG00000205669.2","gene_symbol":"ACOT6","gene_name":"acyl-CoA thioesterase 6 [Source:HGNC Symbol;Acc:HGNC:33159]","synonyms":"C14orf42","biotype":"protein_coding","ncbi_id":"641372","summary":null,"start":73610945,"end":73619888,"strand":1,"description":"acyl-CoA thioesterase 6 [Source:HGNC Symbol;Acc:HGNC:33159]"}, {"versioned_ensembl_gene_id":"ENSG00000162624.14","gene_symbol":"LHX8","gene_name":"LIM homeobox 8 [Source:HGNC Symbol;Acc:HGNC:28838]","synonyms":"Lhx7","biotype":"protein_coding","ncbi_id":"431707","summary":"The protein encoded by this gene is a member of the LIM homeobox family of proteins, which are involved in patterning and differentiation of various tissue types. These proteins contain two tandemly repeated cysteine-rich double-zinc finger motifs known as LIM domains, in addition to a DNA-binding homeodomain. This family member is a transcription factor that plays a role in tooth morphogenesis. It is also involved in oogenesis and in neuronal differentiation. This gene is a candidate gene for cleft palate, and it is also associated with odontoma formation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":75128434,"end":75161533,"strand":1,"description":"LIM homeobox 8 [Source:HGNC Symbol;Acc:HGNC:28838]"}, {"versioned_ensembl_gene_id":"ENSG00000215182.8","gene_symbol":"MUC5AC","gene_name":"mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7515]","synonyms":"MUC5","biotype":"protein_coding","ncbi_id":"4586","summary":null,"start":1157953,"end":1201138,"strand":1,"description":"mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7515]"}, {"versioned_ensembl_gene_id":"ENSG00000231980.1","gene_symbol":"AC011899.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158027373,"end":158031128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236268.5","gene_symbol":"LINC01361","gene_name":"long intergenic non-protein coding RNA 1361 [Source:HGNC Symbol;Acc:HGNC:50595]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927498","summary":null,"start":82973882,"end":82986208,"strand":-1,"description":"long intergenic non-protein coding RNA 1361 [Source:HGNC Symbol;Acc:HGNC:50595]"}, {"versioned_ensembl_gene_id":"ENSG00000277574.2","gene_symbol":"IGHV5-51","gene_name":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28388","summary":null,"start":106603423,"end":106603917,"strand":-1,"description":"immunoglobulin heavy variable 5-51 [Source:HGNC Symbol;Acc:HGNC:5659]"}, {"versioned_ensembl_gene_id":"ENSG00000259271.1","gene_symbol":"ANKRD62P1","gene_name":"ankyrin repeat domain 62 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42363]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107080639","summary":null,"start":16671090,"end":16679493,"strand":-1,"description":"ankyrin repeat domain 62 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42363]"}, {"versioned_ensembl_gene_id":"ENSG00000276261.1","gene_symbol":"AC009509.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27700066,"end":27700574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275903.2","gene_symbol":"PSMB3","gene_name":"proteasome subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:9540]","synonyms":"MGC4147,HC10-II","biotype":"protein_coding","ncbi_id":"5691","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. The 26 S proteasome may be involved in trinucleotide repeat expansion, a phenomenon which is associated with many hereditary neurological diseases. Pseudogenes have been identified on chromosomes 2 and 12. Alternative splicing results in multiple transcript variants [provided by RefSeq, Sep 2013]","start":38553523,"end":38565018,"strand":1,"description":"proteasome subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:9540]"}, {"versioned_ensembl_gene_id":"ENSG00000226516.7","gene_symbol":"FAM138B","gene_name":"family with sequence similarity 138 member B [Source:HGNC Symbol;Acc:HGNC:33582]","synonyms":"F379","biotype":"lincRNA","ncbi_id":"654412","summary":null,"start":113577382,"end":113578852,"strand":1,"description":"family with sequence similarity 138 member B [Source:HGNC Symbol;Acc:HGNC:33582]"}, {"versioned_ensembl_gene_id":"ENSG00000271336.1","gene_symbol":"IGHD1OR15-1A","gene_name":"immunoglobulin heavy diversity 1/OR15-1A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5487]","synonyms":"IGHD1OR151A,IGHD1/OR15-1A","biotype":"IG_D_gene","ncbi_id":"28335","summary":null,"start":20011153,"end":20011169,"strand":-1,"description":"immunoglobulin heavy diversity 1/OR15-1A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5487]"}, {"versioned_ensembl_gene_id":"ENSG00000270104.1","gene_symbol":"AL670729.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":228384114,"end":228385016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234510.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32764544,"end":32765480,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000174332.5","gene_symbol":"GLIS1","gene_name":"GLIS family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:29525]","synonyms":"FLJ36155","biotype":"protein_coding","ncbi_id":"148979","summary":"GLIS1 is a GLI (MIM 165220)-related Kruppel-like zinc finger protein that functions as an activator and repressor of transcription (Kim et al., 2002 [PubMed 12042312]).[supplied by OMIM, Mar 2008]","start":53506237,"end":53738106,"strand":-1,"description":"GLIS family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:29525]"}, {"versioned_ensembl_gene_id":"ENSG00000205704.6","gene_symbol":"LINC00634","gene_name":"long intergenic non-protein coding RNA 634 [Source:HGNC Symbol;Acc:HGNC:27930]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"339674","summary":null,"start":41952165,"end":41958933,"strand":1,"description":"long intergenic non-protein coding RNA 634 [Source:HGNC Symbol;Acc:HGNC:27930]"}, {"versioned_ensembl_gene_id":"ENSG00000251159.1","gene_symbol":"AC093852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44533615,"end":44533880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177432.6","gene_symbol":"NAP1L5","gene_name":"nucleosome assembly protein 1 like 5 [Source:HGNC Symbol;Acc:HGNC:19968]","synonyms":"DRLM","biotype":"protein_coding","ncbi_id":"266812","summary":"This gene encodes a protein that shares sequence similarity to nucleosome assembly factors, but may be localized to the cytoplasm rather than the nucleus. Expression of this gene is downregulated in hepatocellular carcinomas. This gene is located within a differentially methylated region (DMR) and is imprinted and paternally expressed. There is a related pseudogene on chromosome 4. [provided by RefSeq, Nov 2015]","start":88695915,"end":88698235,"strand":-1,"description":"nucleosome assembly protein 1 like 5 [Source:HGNC Symbol;Acc:HGNC:19968]"}, {"versioned_ensembl_gene_id":"ENSG00000249986.1","gene_symbol":"YWHAQP6","gene_name":"YWHAQ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37685]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101290504","summary":null,"start":141600276,"end":141600579,"strand":-1,"description":"YWHAQ pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37685]"}, {"versioned_ensembl_gene_id":"ENSG00000265095.1","gene_symbol":"AC093484.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16391434,"end":16391882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130748.6","gene_symbol":"TMEM160","gene_name":"transmembrane protein 160 [Source:HGNC Symbol;Acc:HGNC:26042]","synonyms":"FLJ20512","biotype":"protein_coding","ncbi_id":"54958","summary":null,"start":47045907,"end":47048630,"strand":-1,"description":"transmembrane protein 160 [Source:HGNC Symbol;Acc:HGNC:26042]"}, {"versioned_ensembl_gene_id":"ENSG00000211625.2","gene_symbol":"IGKV3D-20","gene_name":"immunoglobulin kappa variable 3D-20 [Source:HGNC Symbol;Acc:HGNC:5825]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28874","summary":null,"start":90038848,"end":90039479,"strand":1,"description":"immunoglobulin kappa variable 3D-20 [Source:HGNC Symbol;Acc:HGNC:5825]"}, {"versioned_ensembl_gene_id":"ENSG00000240225.10","gene_symbol":"ZNF542P","gene_name":"zinc finger protein 542, pseudogene [Source:HGNC Symbol;Acc:HGNC:25393]","synonyms":"ZNF542,DKFZp686B2197","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"147947","summary":null,"start":56368099,"end":56379828,"strand":1,"description":"zinc finger protein 542, pseudogene [Source:HGNC Symbol;Acc:HGNC:25393]"}, {"versioned_ensembl_gene_id":"ENSG00000253765.1","gene_symbol":"IGKV2D-19","gene_name":"immunoglobulin kappa variable 2D-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5795]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28887","summary":null,"start":90046796,"end":90047057,"strand":1,"description":"immunoglobulin kappa variable 2D-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5795]"}, {"versioned_ensembl_gene_id":"ENSG00000267192.1","gene_symbol":"AC006116.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56387412,"end":56388424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145337.4","gene_symbol":"PYURF","gene_name":"PIGY upstream reading frame [Source:HGNC Symbol;Acc:HGNC:44317]","synonyms":"PreY","biotype":"protein_coding","ncbi_id":"100996939","summary":"The product of this gene, which is well-conserved, is encoded by the same bicistronic transcript that encodes phosphatidylinositol glycan anchor biosynthesis, class Y, but the two proteins are unrelated. This gene represents the protein encoded by the upstream open reading frame, while the protein encoded by the downstream open reading frame is represented by GeneID:84992. [provided by RefSeq, Aug 2012]","start":88520985,"end":88523813,"strand":-1,"description":"PIGY upstream reading frame [Source:HGNC Symbol;Acc:HGNC:44317]"}, {"versioned_ensembl_gene_id":"ENSG00000234207.1","gene_symbol":"AC096570.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22377594,"end":22482004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223691.1","gene_symbol":"AC068044.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22188336,"end":22190313,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228999.2","gene_symbol":"AC068490.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21942178,"end":21965680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070182.19","gene_symbol":"SPTB","gene_name":"spectrin beta, erythrocytic [Source:HGNC Symbol;Acc:HGNC:11274]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6710","summary":"This locus encodes a member of the spectrin gene family. Spectrin proteins, along with ankyrin, play a role in cell membrane organization and stability. The protein encoded by this locus functions in stability of erythrocyte membranes, and mutations in this gene have been associated with spherocytosis type 2, hereditary elliptocytosis, and neonatal hemolytic anemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2009]","start":64746283,"end":64879883,"strand":-1,"description":"spectrin beta, erythrocytic [Source:HGNC Symbol;Acc:HGNC:11274]"}, {"versioned_ensembl_gene_id":"ENSG00000204532.6","gene_symbol":"ZSCAN5C","gene_name":"zinc finger and SCAN domain containing 5C [Source:HGNC Symbol;Acc:HGNC:34294]","synonyms":"ZSCAN5CP,ZNF495C","biotype":"protein_coding","ncbi_id":"649137","summary":null,"start":56202301,"end":56209452,"strand":1,"description":"zinc finger and SCAN domain containing 5C [Source:HGNC Symbol;Acc:HGNC:34294]"}, {"versioned_ensembl_gene_id":"ENSG00000241478.1","gene_symbol":"HSPA8P9","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402143","summary":null,"start":137880295,"end":137882237,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44924]"}, {"versioned_ensembl_gene_id":"ENSG00000158486.13","gene_symbol":"DNAH3","gene_name":"dynein axonemal heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:2949]","synonyms":"Hsadhc3,Dnahc3b,DLP3,DKFZp434N074","biotype":"protein_coding","ncbi_id":"55567","summary":"This gene belongs to the dynein family, whose members encode large proteins that are constituents of the microtubule-associated motor protein complex. This complex is composed of dynein heavy, intermediate and light chains, which can be axonemal or cytoplasmic. This protein is an axonemal dynein heavy chain. It is involved in producing force for ciliary beating by using energy from ATP hydrolysis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]","start":20933111,"end":21159441,"strand":-1,"description":"dynein axonemal heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:2949]"}, {"versioned_ensembl_gene_id":"ENSG00000265401.1","gene_symbol":"AC093484.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16382152,"end":16382669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233981.1","gene_symbol":"AL022396.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14004920,"end":14006901,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282196.1","gene_symbol":"IGHVII-46-1","gene_name":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]","synonyms":"IGHV(II)-46-1","biotype":"IG_V_pseudogene","ncbi_id":"28365","summary":null,"start":106540499,"end":106540535,"strand":-1,"description":"immunoglobulin heavy variable (II)-46-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5682]"}, {"versioned_ensembl_gene_id":"ENSG00000282494.1","gene_symbol":"AC006449.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38503239,"end":38505534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165288.10","gene_symbol":"BRWD3","gene_name":"bromodomain and WD repeat domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17342]","synonyms":"MRX93,FLJ38568","biotype":"protein_coding","ncbi_id":"254065","summary":"The protein encoded by this gene contains a bromodomain and several WD repeats. It is thought to have a chromatin-modifying function, and may thus play a role in transcription. Mutations in this gene are associated with a spectrum of cognitive disabilities and X-linked macrocephaly. This gene is also associated with translocations in patients with B-cell chronic lymphocytic leukemia. [provided by RefSeq, Jul 2017]","start":80670854,"end":80809688,"strand":-1,"description":"bromodomain and WD repeat domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17342]"}, {"versioned_ensembl_gene_id":"ENSG00000180953.11","gene_symbol":"ST20","gene_name":"suppressor of tumorigenicity 20 [Source:HGNC Symbol;Acc:HGNC:33520]","synonyms":"HCCS-1","biotype":"protein_coding","ncbi_id":"400410","summary":null,"start":79898840,"end":79923702,"strand":-1,"description":"suppressor of tumorigenicity 20 [Source:HGNC Symbol;Acc:HGNC:33520]"}, {"versioned_ensembl_gene_id":"ENSG00000229941.5","gene_symbol":"AC012499.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177698429,"end":177723289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255376.1","gene_symbol":"AP003066.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96642671,"end":96643225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259069.1","gene_symbol":"AL512310.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19677644,"end":19679016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196772.4","gene_symbol":"OR14A16","gene_name":"olfactory receptor family 14 subfamily A member 16 [Source:HGNC Symbol;Acc:HGNC:15022]","synonyms":"OR5AT1","biotype":"protein_coding","ncbi_id":"284532","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247814660,"end":247824119,"strand":-1,"description":"olfactory receptor family 14 subfamily A member 16 [Source:HGNC Symbol;Acc:HGNC:15022]"}, {"versioned_ensembl_gene_id":"ENSG00000231416.1","gene_symbol":"AL358472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153995632,"end":153995960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220868.2","gene_symbol":"MRPL35P1","gene_name":"mitochondrial ribosomal protein L35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29705]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359742","summary":null,"start":13949095,"end":13949666,"strand":1,"description":"mitochondrial ribosomal protein L35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29705]"}, {"versioned_ensembl_gene_id":"ENSG00000227673.1","gene_symbol":"AL162734.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155710098,"end":155710563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232230.1","gene_symbol":"TPM4P1","gene_name":"tropomyosin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45234]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644566","summary":null,"start":100114417,"end":100115223,"strand":-1,"description":"tropomyosin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45234]"}, {"versioned_ensembl_gene_id":"ENSG00000151882.11","gene_symbol":"CCL28","gene_name":"C-C motif chemokine ligand 28 [Source:HGNC Symbol;Acc:HGNC:17700]","synonyms":"SCYA28,MEC,CCK1","biotype":"protein_coding","ncbi_id":"56477","summary":"This antimicrobial gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for resting CD4 or CD8 T cells and eosinophils. The product of this gene binds to chemokine receptors CCR3 and CCR10. This chemokine may play a role in the physiology of extracutaneous epithelial tissues, including diverse mucosal organs. Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":43376645,"end":43412391,"strand":-1,"description":"C-C motif chemokine ligand 28 [Source:HGNC Symbol;Acc:HGNC:17700]"}, {"versioned_ensembl_gene_id":"ENSG00000258436.1","gene_symbol":"RNASE12","gene_name":"ribonuclease A family member 12 (inactive) [Source:HGNC Symbol;Acc:HGNC:24211]","synonyms":"RAI1","biotype":"protein_coding","ncbi_id":"493901","summary":null,"start":20590193,"end":20590823,"strand":-1,"description":"ribonuclease A family member 12 (inactive) [Source:HGNC Symbol;Acc:HGNC:24211]"}, {"versioned_ensembl_gene_id":"ENSG00000267599.1","gene_symbol":"AC008794.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31465653,"end":31466431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105852.10","gene_symbol":"PON3","gene_name":"paraoxonase 3 [Source:HGNC Symbol;Acc:HGNC:9206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5446","summary":"This gene is a member of the paraoxonase family and lies in a cluster on chromosome 7 with the other two family members. The encoded protein is secreted into the bloodstream and associates with high-density lipoprotein (HDL). The protein also rapidly hydrolyzes lactones and can inhibit the oxidation of low-density lipoprotein (LDL), a function that is believed to slow the initiation and progression of atherosclerosis. Alternatively spliced variants which encode different protein isoforms have been described; however, only one has been fully characterized. [provided by RefSeq, Jul 2008]","start":95359944,"end":95396368,"strand":-1,"description":"paraoxonase 3 [Source:HGNC Symbol;Acc:HGNC:9206]"}, {"versioned_ensembl_gene_id":"ENSG00000256258.1","gene_symbol":"AC117500.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131621891,"end":131623203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220326.2","gene_symbol":"AL603865.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121641009,"end":121641221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231200.1","gene_symbol":"LINC01830","gene_name":"long intergenic non-protein coding RNA 1830 [Source:HGNC Symbol;Acc:HGNC:52636]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374322","summary":null,"start":21933336,"end":22531105,"strand":-1,"description":"long intergenic non-protein coding RNA 1830 [Source:HGNC Symbol;Acc:HGNC:52636]"}, {"versioned_ensembl_gene_id":"ENSG00000231204.5","gene_symbol":"AC011752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21317660,"end":21561313,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137332.19","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"RTK6,CD167,NEP,PTK3A,CAK,EDDR1,NTRK4","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30870863,"end":30890046,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000237614.1","gene_symbol":"AC073257.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120542909,"end":120544326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250154.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29738801,"end":29746041,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000251194.2","gene_symbol":"AL133330.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35212550,"end":35214007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242039.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29723740,"end":29724210,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000225206.8","gene_symbol":"MIR137HG","gene_name":"MIR137 host gene [Source:HGNC Symbol;Acc:HGNC:42871]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400765","summary":null,"start":97986740,"end":98049863,"strand":-1,"description":"MIR137 host gene [Source:HGNC Symbol;Acc:HGNC:42871]"}, {"versioned_ensembl_gene_id":"ENSG00000259946.1","gene_symbol":"BX005019.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97967005,"end":97968814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269998.1","gene_symbol":"LINC01930","gene_name":"long intergenic non-protein coding RNA 1930 [Source:HGNC Symbol;Acc:HGNC:52744]","synonyms":"EU358092","biotype":"lincRNA","ncbi_id":"109729128","summary":null,"start":97933474,"end":97941746,"strand":-1,"description":"long intergenic non-protein coding RNA 1930 [Source:HGNC Symbol;Acc:HGNC:52744]"}, {"versioned_ensembl_gene_id":"ENSG00000164898.12","gene_symbol":"FMC1","gene_name":"formation of mitochondrial complex V assembly factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:26946]","synonyms":"C7orf55,HSPC268","biotype":"protein_coding","ncbi_id":"154791","summary":null,"start":139339457,"end":139346319,"strand":1,"description":"formation of mitochondrial complex V assembly factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:26946]"}, {"versioned_ensembl_gene_id":"ENSG00000136014.11","gene_symbol":"USP44","gene_name":"ubiquitin specific peptidase 44 [Source:HGNC Symbol;Acc:HGNC:20064]","synonyms":"FLJ14528","biotype":"protein_coding","ncbi_id":"84101","summary":"The protein encoded by this gene is a protease that functions as a deubiquitinating enzyme. The encoded protein is thought to help regulate the spindle assembly checkpoint by preventing early anaphase onset. This protein specifically deubiquitinates CDC20, which stabilizes the anaphase promoting complex/cyclosome. [provided by RefSeq, Dec 2016]","start":95516560,"end":95551490,"strand":-1,"description":"ubiquitin specific peptidase 44 [Source:HGNC Symbol;Acc:HGNC:20064]"}, {"versioned_ensembl_gene_id":"ENSG00000092529.23","gene_symbol":"CAPN3","gene_name":"calpain 3 [Source:HGNC Symbol;Acc:HGNC:1480]","synonyms":"p94,nCL-1,LGMD2A,LGMD2,CANP3","biotype":"protein_coding","ncbi_id":"825","summary":"Calpain, a heterodimer consisting of a large and a small subunit, is a major intracellular protease, although its function has not been well established. This gene encodes a muscle-specific member of the calpain large subunit family that specifically binds to titin. Mutations in this gene are associated with limb-girdle muscular dystrophies type 2A. Alternate promoters and alternative splicing result in multiple transcript variants encoding different isoforms and some variants are ubiquitously expressed. [provided by RefSeq, Jul 2008]","start":42359500,"end":42412318,"strand":1,"description":"calpain 3 [Source:HGNC Symbol;Acc:HGNC:1480]"}, {"versioned_ensembl_gene_id":"ENSG00000206408.8","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31651454,"end":31656514,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000147065.16","gene_symbol":"MSN","gene_name":"moesin [Source:HGNC Symbol;Acc:HGNC:7373]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4478","summary":"Moesin (for membrane-organizing extension spike protein) is a member of the ERM family which includes ezrin and radixin. ERM proteins appear to function as cross-linkers between plasma membranes and actin-based cytoskeletons. Moesin is localized to filopodia and other membranous protrusions that are important for cell-cell recognition and signaling and for cell movement. [provided by RefSeq, Jul 2008]","start":65588377,"end":65741931,"strand":1,"description":"moesin [Source:HGNC Symbol;Acc:HGNC:7373]"}, {"versioned_ensembl_gene_id":"ENSG00000282552.1","gene_symbol":"IGHVII-33-1","gene_name":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]","synonyms":"IGHV(II)-33-1","biotype":"IG_V_pseudogene","ncbi_id":"28369","summary":null,"start":106392066,"end":106392345,"strand":-1,"description":"immunoglobulin heavy variable (II)-33-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5678]"}, {"versioned_ensembl_gene_id":"ENSG00000250950.1","gene_symbol":"AC093752.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119456350,"end":119457277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246203.2","gene_symbol":"AL353807.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155614726,"end":155660245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237767.1","gene_symbol":"LINC01370","gene_name":"long intergenic non-protein coding RNA 1370 [Source:HGNC Symbol;Acc:HGNC:50608]","synonyms":"HI-LNC25","biotype":"lincRNA","ncbi_id":"100505663","summary":null,"start":40004477,"end":40008529,"strand":1,"description":"long intergenic non-protein coding RNA 1370 [Source:HGNC Symbol;Acc:HGNC:50608]"}, {"versioned_ensembl_gene_id":"ENSG00000234878.1","gene_symbol":"HSPE1P1","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16530]","synonyms":"HSPEP1,bA101E14.1","biotype":"processed_pseudogene","ncbi_id":"140895","summary":null,"start":39932922,"end":39933239,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16530]"}, {"versioned_ensembl_gene_id":"ENSG00000225075.1","gene_symbol":"AL603832.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112693688,"end":112696621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228202.1","gene_symbol":"CR788234.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745422,"end":29745646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258640.3","gene_symbol":"RPL21P5","gene_name":"ribosomal protein L21 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23541]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641613","summary":null,"start":31111569,"end":31112239,"strand":-1,"description":"ribosomal protein L21 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23541]"}, {"versioned_ensembl_gene_id":"ENSG00000171053.9","gene_symbol":"PATE1","gene_name":"prostate and testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24664]","synonyms":"PATE","biotype":"protein_coding","ncbi_id":"160065","summary":null,"start":125746293,"end":125749867,"strand":1,"description":"prostate and testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24664]"}, {"versioned_ensembl_gene_id":"ENSG00000279182.1","gene_symbol":"CR559946.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50316035,"end":50317025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243257.1","gene_symbol":"MTCO2P29","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52158]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075194","summary":null,"start":120722458,"end":120722646,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52158]"}, {"versioned_ensembl_gene_id":"ENSG00000163083.5","gene_symbol":"INHBB","gene_name":"inhibin beta B subunit [Source:HGNC Symbol;Acc:HGNC:6067]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3625","summary":"This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate a subunit of the dimeric activin and inhibin protein complexes. These complexes activate and inhibit, respectively, follicle stimulating hormone secretion from the pituitary gland. Polymorphisms near this gene are associated with pre-eclampsia in female human patients. [provided by RefSeq, Aug 2016]","start":120346143,"end":120351808,"strand":1,"description":"inhibin beta B subunit [Source:HGNC Symbol;Acc:HGNC:6067]"}, {"versioned_ensembl_gene_id":"ENSG00000091436.16","gene_symbol":"MAP3K20","gene_name":"mitogen-activated protein kinase kinase kinase 20 [Source:HGNC Symbol;Acc:HGNC:17797]","synonyms":"ZAK,MRK,MLTKbeta,MLTKalpha,MLTK,MLK7","biotype":"protein_coding","ncbi_id":"51776","summary":"This gene is a member of the MAPKKK family of signal transduction molecules and encodes a protein with an N-terminal kinase catalytic domain, followed by a leucine zipper motif and a sterile-alpha motif (SAM). This magnesium-binding protein forms homodimers and is located in the cytoplasm. The protein mediates gamma radiation signaling leading to cell cycle arrest and activity of this protein plays a role in cell cycle checkpoint regulation in cells. The protein also has pro-apoptotic activity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":173075435,"end":173268010,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 20 [Source:HGNC Symbol;Acc:HGNC:17797]"}, {"versioned_ensembl_gene_id":"ENSG00000254864.1","gene_symbol":"AC107884.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7568866,"end":7572046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225882.1","gene_symbol":"LINC01456","gene_name":"long intergenic non-protein coding RNA 1456 [Source:HGNC Symbol;Acc:HGNC:50846]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373144","summary":null,"start":17970197,"end":18104644,"strand":-1,"description":"long intergenic non-protein coding RNA 1456 [Source:HGNC Symbol;Acc:HGNC:50846]"}, {"versioned_ensembl_gene_id":"ENSG00000248387.1","gene_symbol":"AC121161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158469586,"end":158470702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070019.4","gene_symbol":"GUCY2C","gene_name":"guanylate cyclase 2C [Source:HGNC Symbol;Acc:HGNC:4688]","synonyms":"STAR,GUC2C","biotype":"protein_coding","ncbi_id":"2984","summary":"This gene encodes a transmembrane protein that functions as a receptor for endogenous peptides guanylin and uroguanylin, and the heat-stable E. coli enterotoxin. The encoded protein activates the cystic fibrosis transmembrane conductance regulator. Mutations in this gene are associated with familial diarrhea (autosomal dominant) and meconium ileus (autosomal recessive). [provided by RefSeq, Nov 2016]","start":14612632,"end":14696585,"strand":-1,"description":"guanylate cyclase 2C [Source:HGNC Symbol;Acc:HGNC:4688]"}, {"versioned_ensembl_gene_id":"ENSG00000104055.15","gene_symbol":"TGM5","gene_name":"transglutaminase 5 [Source:HGNC Symbol;Acc:HGNC:11781]","synonyms":"TGX","biotype":"protein_coding","ncbi_id":"9333","summary":"This gene encodes a member of the transglutaminase family. The encoded protein catalyzes formation of protein cross-links between glutamine and lysine residues, often resulting in stabilization of protein assemblies. This reaction is calcium dependent. Mutations in this gene have been associated with acral peeling skin syndrome. [provided by RefSeq, Oct 2009]","start":43232595,"end":43266857,"strand":-1,"description":"transglutaminase 5 [Source:HGNC Symbol;Acc:HGNC:11781]"}, {"versioned_ensembl_gene_id":"ENSG00000148356.13","gene_symbol":"LRSAM1","gene_name":"leucine rich repeat and sterile alpha motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25135]","synonyms":"FLJ31641,CMT2P","biotype":"protein_coding","ncbi_id":"90678","summary":"This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self-ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jan 2012]","start":127451486,"end":127503501,"strand":1,"description":"leucine rich repeat and sterile alpha motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25135]"}, {"versioned_ensembl_gene_id":"ENSG00000282750.1","gene_symbol":"TBC1D3B","gene_name":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]","synonyms":"PRC17,TBC1D3I,PRC17,TBC1D3I","biotype":"unprocessed_pseudogene","ncbi_id":"414059","summary":"This gene encodes a protein that is similar to TBC1 domain family, member 3. This protein contains a TBC (Tre-2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q. [provided by RefSeq, Apr 2009]","start":36165687,"end":36176601,"strand":-1,"description":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]"}, {"versioned_ensembl_gene_id":"ENSG00000243566.6","gene_symbol":"UPK3B","gene_name":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]","synonyms":"UPIIIb,p35,MGC10902,FLJ32198","biotype":"protein_coding","ncbi_id":"105375355","summary":"UPK3B is a minor component of the apical plaques of mammalian urothelium that binds and dimerizes with uroplakin-1b (UPK1B; MIM 602380), one of the major conserved urothelium membrane proteins. The other major conserved integral membrane proteins of urothelial plaques are UPK1A (MIM 611557), UPK2 (MIM 611558), and UPK3A (MIM 611559) (Deng et al., 2002 [PubMed 12446744]).[supplied by OMIM, Mar 2008]","start":76510428,"end":76516521,"strand":1,"description":"uroplakin 3B [Source:HGNC Symbol;Acc:HGNC:21444]"}, {"versioned_ensembl_gene_id":"ENSG00000280418.1","gene_symbol":"AC007326.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18951934,"end":18959512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225066.1","gene_symbol":"Z93929.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17933349,"end":17934823,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282642.1","gene_symbol":"IGHV3-33","gene_name":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28434","summary":null,"start":106359784,"end":106360304,"strand":-1,"description":"immunoglobulin heavy variable 3-33 [Source:HGNC Symbol;Acc:HGNC:5596]"}, {"versioned_ensembl_gene_id":"ENSG00000276467.1","gene_symbol":"Z93929.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17897711,"end":17900333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281983.1","gene_symbol":"IGHV3-29","gene_name":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28440","summary":null,"start":106356982,"end":106357409,"strand":-1,"description":"immunoglobulin heavy variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5590]"}, {"versioned_ensembl_gene_id":"ENSG00000266969.1","gene_symbol":"AP002449.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12984694,"end":12991173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282761.1","gene_symbol":"AC234301.5","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106355443,"end":106355479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282404.1","gene_symbol":"IGHV4-31","gene_name":"immunoglobulin heavy variable 4-31 [Source:HGNC Symbol;Acc:HGNC:5649]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28396","summary":null,"start":106350054,"end":106350526,"strand":-1,"description":"immunoglobulin heavy variable 4-31 [Source:HGNC Symbol;Acc:HGNC:5649]"}, {"versioned_ensembl_gene_id":"ENSG00000257545.4","gene_symbol":"AC079385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106495958,"end":106774918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282356.1","gene_symbol":"IGHV3-30-2","gene_name":"immunoglobulin heavy variable 3-30-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5592]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28438","summary":null,"start":106345166,"end":106345604,"strand":-1,"description":"immunoglobulin heavy variable 3-30-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5592]"}, {"versioned_ensembl_gene_id":"ENSG00000121316.10","gene_symbol":"PLBD1","gene_name":"phospholipase B domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26215]","synonyms":"FLJ22662","biotype":"protein_coding","ncbi_id":"79887","summary":null,"start":14503661,"end":14568349,"strand":-1,"description":"phospholipase B domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26215]"}, {"versioned_ensembl_gene_id":"ENSG00000255649.1","gene_symbol":"AC008114.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14530151,"end":14533229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196132.11","gene_symbol":"MYT1","gene_name":"myelin transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7622]","synonyms":"ZC2H2C1,PLPB1,NZF2,MYTI,MTF1,ZC2HC4A","biotype":"protein_coding","ncbi_id":"4661","summary":"The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system. [provided by RefSeq, Jul 2008]","start":64151791,"end":64242253,"strand":1,"description":"myelin transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7622]"}, {"versioned_ensembl_gene_id":"ENSG00000214772.2","gene_symbol":"AC010168.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14665655,"end":14757963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258461.5","gene_symbol":"AC012651.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42348103,"end":42412317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158435.7","gene_symbol":"CNOT11","gene_name":"CCR4-NOT transcription complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:25217]","synonyms":"C40,C2orf29","biotype":"protein_coding","ncbi_id":"55571","summary":null,"start":101252802,"end":101270316,"strand":1,"description":"CCR4-NOT transcription complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:25217]"}, {"versioned_ensembl_gene_id":"ENSG00000230138.1","gene_symbol":"AC119428.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53366668,"end":53368245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276888.1","gene_symbol":"AL512624.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19420975,"end":19425017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182768.8","gene_symbol":"NGRN","gene_name":"neugrin, neurite outgrowth associated [Source:HGNC Symbol;Acc:HGNC:18077]","synonyms":"DSC92","biotype":"protein_coding","ncbi_id":"51335","summary":null,"start":90265659,"end":90278141,"strand":1,"description":"neugrin, neurite outgrowth associated [Source:HGNC Symbol;Acc:HGNC:18077]"}, {"versioned_ensembl_gene_id":"ENSG00000235840.1","gene_symbol":"AC012363.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120319007,"end":120326298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234189.1","gene_symbol":"AC099799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22317053,"end":22317244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277833.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769756,"end":54784259,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000228181.1","gene_symbol":"AL590365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15171036,"end":15171278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163382.11","gene_symbol":"NAXE","gene_name":"NAD(P)HX epimerase [Source:HGNC Symbol;Acc:HGNC:18453]","synonyms":"MGC119145,MGC119144,MGC119143,APOA1BP,AIBP,YJEFN1","biotype":"protein_coding","ncbi_id":"128240","summary":"The product of this gene interacts with apolipoprotein A-I (apoA-I), the major apolipoprotein of high-density lipoproteins (HDLs). It is secreted into some bodily fluids, and its synthesis and secretion are stimulated in vitro by incubating cells with apoA-I. The human genome contains related pseudogenes. [provided by RefSeq, Jul 2008]","start":156591762,"end":156594299,"strand":1,"description":"NAD(P)HX epimerase [Source:HGNC Symbol;Acc:HGNC:18453]"}, {"versioned_ensembl_gene_id":"ENSG00000116791.13","gene_symbol":"CRYZ","gene_name":"crystallin zeta [Source:HGNC Symbol;Acc:HGNC:2419]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1429","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. The former class is also called phylogenetically-restricted crystallins. This gene encodes a taxon-specific crystallin protein which has NADPH-dependent quinone reductase activity distinct from other known quinone reductases. It lacks alcohol dehydrogenase activity although by similarity it is considered a member of the zinc-containing alcohol dehydrogenase family. Unlike other mammalian species, in humans, lens expression is low. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. One pseudogene is known to exist. [provided by RefSeq, Sep 2008]","start":74705482,"end":74733408,"strand":-1,"description":"crystallin zeta [Source:HGNC Symbol;Acc:HGNC:2419]"}, {"versioned_ensembl_gene_id":"ENSG00000232009.1","gene_symbol":"AL591503.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47389961,"end":47392300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143006.7","gene_symbol":"DMRTB1","gene_name":"DMRT like family B with proline rich C-terminal 1 [Source:HGNC Symbol;Acc:HGNC:13913]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63948","summary":null,"start":53459399,"end":53467488,"strand":1,"description":"DMRT like family B with proline rich C-terminal 1 [Source:HGNC Symbol;Acc:HGNC:13913]"}, {"versioned_ensembl_gene_id":"ENSG00000160505.15","gene_symbol":"NLRP4","gene_name":"NLR family pyrin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:22943]","synonyms":"RNH2,PYPAF4,PAN2,NALP4,FLJ32126,CT58,CLR19.5","biotype":"protein_coding","ncbi_id":"147945","summary":"The protein encoded by this gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). This gene product has a demonstrated role as a negative regulator of autophagy and type I interferon signaling pathways as a result of protein interactions with its NACHT domain. The PYD domain has also been shown to be important in the inhibition of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells). [provided by RefSeq, Dec 2016]","start":55836578,"end":55881854,"strand":1,"description":"NLR family pyrin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:22943]"}, {"versioned_ensembl_gene_id":"ENSG00000180834.7","gene_symbol":"MAP6D1","gene_name":"MAP6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25753]","synonyms":"SL21,FLJ12748","biotype":"protein_coding","ncbi_id":"79929","summary":"This gene encodes a protein highly similar to the mouse MAP6 domain containing 1 protein, which is related to the STOP proteins. Based on the study of the mouse protein, the encoded protein may function as a calmodulin-regulated neuronal protein that binds and stabilizes microtubules but also associates with the Golgi membranes through N-terminal palmitoylation. [provided by RefSeq, Oct 2008]","start":183815876,"end":183825594,"strand":-1,"description":"MAP6 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25753]"}, {"versioned_ensembl_gene_id":"ENSG00000254156.1","gene_symbol":"MTND6P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39483]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106478952","summary":null,"start":46838788,"end":46839205,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39483]"}, {"versioned_ensembl_gene_id":"ENSG00000270422.1","gene_symbol":"AL133247.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31651381,"end":31651862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270941.1","gene_symbol":"AC006254.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52734735,"end":52735013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275674.1","gene_symbol":"AC091167.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":90266317,"end":90314499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240452.1","gene_symbol":"MTCO1P29","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52094]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075225","summary":null,"start":120722024,"end":120722311,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52094]"}, {"versioned_ensembl_gene_id":"ENSG00000229424.1","gene_symbol":"AC007349.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36750687,"end":36763081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270322.1","gene_symbol":"AC091167.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90281848,"end":90282031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071242.11","gene_symbol":"RPS6KA2","gene_name":"ribosomal protein S6 kinase A2 [Source:HGNC Symbol;Acc:HGNC:10431]","synonyms":"RSK3,RSK,HU-2","biotype":"protein_coding","ncbi_id":"6196","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains two non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Alternative splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jan 2016]","start":166409364,"end":166906451,"strand":-1,"description":"ribosomal protein S6 kinase A2 [Source:HGNC Symbol;Acc:HGNC:10431]"}, {"versioned_ensembl_gene_id":"ENSG00000114904.12","gene_symbol":"NEK4","gene_name":"NIMA related kinase 4 [Source:HGNC Symbol;Acc:HGNC:11399]","synonyms":"STK2,pp12301,NRK2","biotype":"protein_coding","ncbi_id":"6787","summary":"The protein encoded by this gene is a serine/threonine protein kinase required for normal entry into replicative senescence. The encoded protein also is involved in cell cycle arrest in response to double-stranded DNA damage. Finally, this protein plays a role in maintaining cilium integrity, and defects in this gene have been associated with ciliopathies. [provided by RefSeq, Jan 2017]","start":52708449,"end":52770949,"strand":-1,"description":"NIMA related kinase 4 [Source:HGNC Symbol;Acc:HGNC:11399]"}, {"versioned_ensembl_gene_id":"ENSG00000239722.1","gene_symbol":"IMP3P2","gene_name":"IMP3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49386]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480272","summary":null,"start":128693450,"end":128693924,"strand":1,"description":"IMP3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49386]"}, {"versioned_ensembl_gene_id":"ENSG00000271137.1","gene_symbol":"AC006254.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52753526,"end":52754690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276084.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724447,"end":54736085,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000160218.12","gene_symbol":"TRAPPC10","gene_name":"trafficking protein particle complex 10 [Source:HGNC Symbol;Acc:HGNC:11868]","synonyms":"TRS130,TMEM1,EHOC-1","biotype":"protein_coding","ncbi_id":"7109","summary":"The protein encoded by this gene is a transmembrane protein found in the cis-Golgi complex. The encoded protein is part of the multisubunit transport protein particle (TRAPP) complex and may be involved in vesicular transport from the endoplasmic reticulum to the Golgi. Mutations in this gene could be responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy, or for autoimmune polyglandular disease type 1. [provided by RefSeq, Jul 2008]","start":44012319,"end":44106552,"strand":1,"description":"trafficking protein particle complex 10 [Source:HGNC Symbol;Acc:HGNC:11868]"}, {"versioned_ensembl_gene_id":"ENSG00000235272.1","gene_symbol":"FAM103A2P","gene_name":"family with sequence similarity 103 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:21234]","synonyms":"dJ427A4.2,C6orf119","biotype":"processed_pseudogene","ncbi_id":"353267","summary":null,"start":166586124,"end":166586477,"strand":-1,"description":"family with sequence similarity 103 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:21234]"}, {"versioned_ensembl_gene_id":"ENSG00000231982.1","gene_symbol":"AC112907.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":186826549,"end":186827337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223947.1","gene_symbol":"AC016738.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100993676,"end":101002244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249141.1","gene_symbol":"AL159163.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":166858094,"end":166956124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274402.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738465,"end":54752989,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000253828.3","gene_symbol":"MTND2P38","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52069]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075276","summary":null,"start":46827228,"end":46827894,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52069]"}, {"versioned_ensembl_gene_id":"ENSG00000272902.2","gene_symbol":"TBC1D8-AS1","gene_name":"TBC1 domain family member 8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52782]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506286","summary":null,"start":101151660,"end":101155412,"strand":1,"description":"TBC1 domain family member 8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52782]"}, {"versioned_ensembl_gene_id":"ENSG00000232082.1","gene_symbol":"RPS6KA2-IT1","gene_name":"RPS6KA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41378]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874353","summary":null,"start":166460663,"end":166465383,"strand":-1,"description":"RPS6KA2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41378]"}, {"versioned_ensembl_gene_id":"ENSG00000277893.1","gene_symbol":"SRD5A2","gene_name":"steroid 5 alpha-reductase 2 [Source:HGNC Symbol;Acc:HGNC:11285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6716","summary":"This gene encodes a microsomal protein expressed at high levels in androgen-sensitive tissues such as the prostate. The encoded protein is active at acidic pH and is sensitive to the 4-azasteroid inhibitor finasteride. Deficiencies in this gene can result in male pseudohermaphroditism, specifically pseudovaginal perineoscrotal hypospadias (PPSH). [provided by RefSeq, Jul 2008]","start":31522480,"end":31581067,"strand":-1,"description":"steroid 5 alpha-reductase 2 [Source:HGNC Symbol;Acc:HGNC:11285]"}, {"versioned_ensembl_gene_id":"ENSG00000258665.1","gene_symbol":"AC068831.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91031712,"end":91032435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258542.1","gene_symbol":"AC068831.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":91029888,"end":91029996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275345.1","gene_symbol":"AC091167.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90281858,"end":90282270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116922.14","gene_symbol":"C1orf109","gene_name":"chromosome 1 open reading frame 109 [Source:HGNC Symbol;Acc:HGNC:26039]","synonyms":"FLJ20508","biotype":"protein_coding","ncbi_id":"54955","summary":null,"start":37681570,"end":37692249,"strand":-1,"description":"chromosome 1 open reading frame 109 [Source:HGNC Symbol;Acc:HGNC:26039]"}, {"versioned_ensembl_gene_id":"ENSG00000267662.1","gene_symbol":"AC025809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31348881,"end":31417794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214432.9","gene_symbol":"AC068831.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91022619,"end":91036611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105983.20","gene_symbol":"LMBR1","gene_name":"limb development membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13243]","synonyms":"ZRS,FLJ11665,C7orf2,ACHP","biotype":"protein_coding","ncbi_id":"64327","summary":"This gene encodes a member of the LMBR1-like membrane protein family. Another member of this protein family has been shown to be a lipocalin transmembrane receptor. A highly conserved, cis-acting regulatory module for the sonic hedgehog gene is located within an intron of this gene. Consequently, disruption of this genic region can alter sonic hedgehog expression and affect limb patterning, but it is not known if this gene functions directly in limb development. Mutations and chromosomal deletions and rearrangements in this genic region are associated with acheiropody and preaxial polydactyly, which likely result from altered sonic hedgehog expression. [provided by RefSeq, Jul 2008]","start":156668946,"end":156893230,"strand":-1,"description":"limb development membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13243]"}, {"versioned_ensembl_gene_id":"ENSG00000267777.1","gene_symbol":"LINC01791","gene_name":"long intergenic non-protein coding RNA 1791 [Source:HGNC Symbol;Acc:HGNC:52581]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985312","summary":null,"start":31167516,"end":31207663,"strand":1,"description":"long intergenic non-protein coding RNA 1791 [Source:HGNC Symbol;Acc:HGNC:52581]"}, {"versioned_ensembl_gene_id":"ENSG00000240766.1","gene_symbol":"PLCXD2-AS1","gene_name":"PLCXD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41145]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874115","summary":null,"start":111676736,"end":111677433,"strand":-1,"description":"PLCXD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41145]"}, {"versioned_ensembl_gene_id":"ENSG00000092377.13","gene_symbol":"TBL1Y","gene_name":"transducin beta like 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:18502]","synonyms":"TBL1","biotype":"protein_coding","ncbi_id":"90665","summary":"The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This gene is highly similar to TBL1X gene in nucleotide sequence and protein sequence, but the TBL1X gene is located on chromosome X and this gene is on chromosome Y. This gene has three alternatively spliced transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":6910686,"end":7091683,"strand":1,"description":"transducin beta like 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:18502]"}, {"versioned_ensembl_gene_id":"ENSG00000227597.1","gene_symbol":"WASF1P1","gene_name":"WASF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51533]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131624","summary":null,"start":108276812,"end":108277942,"strand":1,"description":"WASF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51533]"}, {"versioned_ensembl_gene_id":"ENSG00000162813.17","gene_symbol":"BPNT1","gene_name":"3'(2'), 5'-bisphosphate nucleotidase 1 [Source:HGNC Symbol;Acc:HGNC:1096]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10380","summary":"BPNT1, also called bisphosphate 3-prime-nucleotidase, or BPntase, is a member of a magnesium-dependent phosphomonoesterase family. Lithium, a major drug used to treat manic depression, acts as an uncompetitive inhibitor of BPntase. The predicted human protein is 92% identical to mouse BPntase. BPntase's physiologic role in nucleotide metabolism may be regulated by inositol signaling pathways. The inhibition of human BPntase may account for lithium-induced nephrotoxicity. [provided by RefSeq, Jul 2008]","start":220057482,"end":220090462,"strand":-1,"description":"3'(2'), 5'-bisphosphate nucleotidase 1 [Source:HGNC Symbol;Acc:HGNC:1096]"}, {"versioned_ensembl_gene_id":"ENSG00000273906.1","gene_symbol":"AC011297.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6918682,"end":6920791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185043.10","gene_symbol":"CIB1","gene_name":"calcium and integrin binding 1 [Source:HGNC Symbol;Acc:HGNC:16920]","synonyms":"SIP2-28,KIP,CIB","biotype":"protein_coding","ncbi_id":"10519","summary":"This gene encodes a member of the EF-hand domain-containing calcium-binding superfamily. The encoded protein interacts with many other proteins, including the platelet integrin alpha-IIb-beta-3, DNA-dependent protein kinase, presenilin-2, focal adhesion kinase, p21 activated kinase, and protein kinase D. The encoded protein may be involved in cell survival and proliferation, and is associated with several disease states including cancer and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":90229975,"end":90234047,"strand":-1,"description":"calcium and integrin binding 1 [Source:HGNC Symbol;Acc:HGNC:16920]"}, {"versioned_ensembl_gene_id":"ENSG00000030066.13","gene_symbol":"NUP160","gene_name":"nucleoporin 160 [Source:HGNC Symbol;Acc:HGNC:18017]","synonyms":"KIAA0197,FLJ22583","biotype":"protein_coding","ncbi_id":"23279","summary":"NUP160 is 1 of up to 60 proteins that make up the 120-MD nuclear pore complex, which mediates nucleoplasmic transport.[supplied by OMIM, Apr 2004]","start":47778087,"end":47848555,"strand":-1,"description":"nucleoporin 160 [Source:HGNC Symbol;Acc:HGNC:18017]"}, {"versioned_ensembl_gene_id":"ENSG00000228751.1","gene_symbol":"AC004022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95350164,"end":95351229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271543.1","gene_symbol":"AC021443.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47796169,"end":47796379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179873.14","gene_symbol":"NLRP11","gene_name":"NLR family pyrin domain containing 11 [Source:HGNC Symbol;Acc:HGNC:22945]","synonyms":"PAN10,NOD17,NALP11,CLR19.6,PYPAF6","biotype":"protein_coding","ncbi_id":"204801","summary":"This gene is a member of the the NOD-like receptor protein (NLRP) gene family and encodes a protein with an N-terminal pyrin death (PYD) domain and nucleoside triphosphate hydrolase (NACHT) domain and a C-terminal leucine-rich repeats (LRR) region. This gene has been shown to regulate caspases in the proinflammatory signal transduction pathway and, based on studies of other members of the NLRP gene family with similar domain structure, is predicted to form part of the multiprotein inflammasome complex. Alternative splicing produces multiple transcript variants encoding distince isoforms. [provided by RefSeq, May 2017]","start":55785397,"end":55836800,"strand":-1,"description":"NLR family pyrin domain containing 11 [Source:HGNC Symbol;Acc:HGNC:22945]"}, {"versioned_ensembl_gene_id":"ENSG00000229733.1","gene_symbol":"AL030996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123558350,"end":123558584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274476.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR2DL6,KIRY,KIRZ,KIR15","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754923,"end":54767817,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000259943.1","gene_symbol":"AL050341.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40256427,"end":40257967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128011.4","gene_symbol":"LRFN1","gene_name":"leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29290]","synonyms":"SALM2,KIAA1484","biotype":"protein_coding","ncbi_id":"57622","summary":null,"start":39306568,"end":39315336,"strand":-1,"description":"leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29290]"}, {"versioned_ensembl_gene_id":"ENSG00000213471.10","gene_symbol":"TTLL13P","gene_name":"tubulin tyrosine ligase like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32484]","synonyms":"TTLL13,MGC33417,FLJ46079","biotype":"protein_coding","ncbi_id":"440307","summary":null,"start":90249530,"end":90265482,"strand":1,"description":"tubulin tyrosine ligase like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32484]"}, {"versioned_ensembl_gene_id":"ENSG00000150990.7","gene_symbol":"DHX37","gene_name":"DEAH-box helicase 37 [Source:HGNC Symbol;Acc:HGNC:17210]","synonyms":"MGC4322,MGC2695,KIAA1517,Dhr1,DDX37","biotype":"protein_coding","ncbi_id":"57647","summary":"This gene encodes a DEAD box protein. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. [provided by RefSeq, Jul 2008]","start":124946825,"end":124989122,"strand":-1,"description":"DEAH-box helicase 37 [Source:HGNC Symbol;Acc:HGNC:17210]"}, {"versioned_ensembl_gene_id":"ENSG00000244657.1","gene_symbol":"AC008267.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66485095,"end":66486532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196549.10","gene_symbol":"MME","gene_name":"membrane metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:7154]","synonyms":"NEP,CD10,CALLA","biotype":"protein_coding","ncbi_id":"4311","summary":"The protein encoded by this gene is a type II transmembrane glycoprotein and a common acute lymphocytic leukemia antigen that is an important cell surface marker in the diagnosis of human acute lymphocytic leukemia (ALL). The encoded protein is present on leukemic cells of pre-B phenotype, which represent 85% of cases of ALL. This protein is not restricted to leukemic cells, however, and is found on a variety of normal tissues. The protein is a neutral endopeptidase that cleaves peptides at the amino side of hydrophobic residues and inactivates several peptide hormones including glucagon, enkephalins, substance P, neurotensin, oxytocin, and bradykinin. [provided by RefSeq, Aug 2017]","start":155024124,"end":155183729,"strand":1,"description":"membrane metalloendopeptidase [Source:HGNC Symbol;Acc:HGNC:7154]"}, {"versioned_ensembl_gene_id":"ENSG00000278867.1","gene_symbol":"AC090616.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32051030,"end":32053208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260668.1","gene_symbol":"AC093536.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64260570,"end":64261239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261028.1","gene_symbol":"AC012322.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64242608,"end":64343909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280866.1","gene_symbol":"IGLV3-32","gene_name":"immunoglobulin lambda variable 3-32 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5914]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28787","summary":null,"start":22603633,"end":22604161,"strand":1,"description":"immunoglobulin lambda variable 3-32 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5914]"}, {"versioned_ensembl_gene_id":"ENSG00000228569.1","gene_symbol":"AC073133.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156432523,"end":156435833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233878.1","gene_symbol":"AC073133.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156437789,"end":156445588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153487.12","gene_symbol":"ING1","gene_name":"inhibitor of growth family member 1 [Source:HGNC Symbol;Acc:HGNC:6062]","synonyms":"p47ING1a,p47,p33ING1b,p33ING1,p33,p24ING1c","biotype":"protein_coding","ncbi_id":"3621","summary":"This gene encodes a tumor suppressor protein that can induce cell growth arrest and apoptosis. The encoded protein is a nuclear protein that physically interacts with the tumor suppressor protein TP53 and is a component of the p53 signaling pathway. Reduced expression and rearrangement of this gene have been detected in various cancers. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":110712736,"end":110723339,"strand":1,"description":"inhibitor of growth family member 1 [Source:HGNC Symbol;Acc:HGNC:6062]"}, {"versioned_ensembl_gene_id":"ENSG00000267378.1","gene_symbol":"AC020897.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30946582,"end":30957192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005421.8","gene_symbol":"PON1","gene_name":"paraoxonase 1 [Source:HGNC Symbol;Acc:HGNC:9204]","synonyms":"PON,ESA","biotype":"protein_coding","ncbi_id":"5444","summary":"This gene encodes a member of the paraoxonase family of enzymes and exhibits lactonase and ester hydrolase activity. Following synthesis in the kidney and liver, the enzyme is secreted into the circulation, where it binds to high density lipoprotein (HDL) particles and hydrolyzes thiolactones and xenobiotics, including paraoxon, a metabolite of the insecticide parathion. Polymorphisms in this gene may be associated with coronary artery disease and diabetic retinopathy. The gene is found in a cluster of three related paraoxonase genes on chromosome 7. [provided by RefSeq, Aug 2017]","start":95297676,"end":95324707,"strand":-1,"description":"paraoxonase 1 [Source:HGNC Symbol;Acc:HGNC:9204]"}, {"versioned_ensembl_gene_id":"ENSG00000235829.1","gene_symbol":"TBCAP2","gene_name":"tubulin folding cofactor A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"494541","summary":null,"start":14692129,"end":14692613,"strand":-1,"description":"tubulin folding cofactor A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42631]"}, {"versioned_ensembl_gene_id":"ENSG00000260715.1","gene_symbol":"AC093536.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64155169,"end":64156574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234593.2","gene_symbol":"AL359873.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14348955,"end":14391575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281055.1","gene_symbol":"IGLV2-34","gene_name":"immunoglobulin lambda variable 2-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5893]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28810","summary":null,"start":22588947,"end":22589401,"strand":1,"description":"immunoglobulin lambda variable 2-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5893]"}, {"versioned_ensembl_gene_id":"ENSG00000278567.2","gene_symbol":"CCL3","gene_name":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]","synonyms":"SCYA3,MIP-1-alpha,LD78ALPHA,G0S19-1","biotype":"protein_coding","ncbi_id":"6348","summary":"This locus represents a small inducible cytokine. The encoded protein, also known as macrophage inflammatory protein 1 alpha, plays a role in inflammatory responses through binding to the receptors CCR1, CCR4 and CCR5. Polymorphisms at this locus may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1.[provided by RefSeq, Sep 2010]","start":36088256,"end":36090169,"strand":-1,"description":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]"}, {"versioned_ensembl_gene_id":"ENSG00000231234.2","gene_symbol":"SKP1P1","gene_name":"S-phase kinase associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33696]","synonyms":"TCEB1P,TCEB1L,OCP2,EMC19","biotype":"transcribed_processed_pseudogene","ncbi_id":"6922","summary":null,"start":66423405,"end":66423893,"strand":-1,"description":"S-phase kinase associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33696]"}, {"versioned_ensembl_gene_id":"ENSG00000261653.1","gene_symbol":"AC092337.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63935778,"end":63936906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267735.1","gene_symbol":"AC020934.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12880969,"end":12884088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216775.2","gene_symbol":"AL109918.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52665148,"end":52669155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175147.11","gene_symbol":"TMEM51-AS1","gene_name":"TMEM51 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26301]","synonyms":"FLJ23703,C1orf126","biotype":"antisense_RNA","ncbi_id":"200197","summary":null,"start":15111815,"end":15152464,"strand":-1,"description":"TMEM51 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26301]"}, {"versioned_ensembl_gene_id":"ENSG00000100162.14","gene_symbol":"CENPM","gene_name":"centromere protein M [Source:HGNC Symbol;Acc:HGNC:18352]","synonyms":"Pane1,MGC861,CENP-M,C22orf18","biotype":"protein_coding","ncbi_id":"79019","summary":"The protein encoded by this gene is an inner protein of the kinetochore, the multi-protein complex that binds spindle microtubules to regulate chromosome segregation during cell division. It belongs to the constitutive centromere-associated network protein group, whose members interact with outer kinetochore proteins and help to maintain centromere identity at each cell division cycle. The protein is structurally related to GTPases but cannot bind guanosine triphosphate. A point mutation that affects interaction with another constitutive centromere-associated network protein, CENP-I, impairs kinetochore assembly and chromosome alignment, suggesting that it is required for kinetochore formation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":41938721,"end":41947164,"strand":-1,"description":"centromere protein M [Source:HGNC Symbol;Acc:HGNC:18352]"}, {"versioned_ensembl_gene_id":"ENSG00000133115.11","gene_symbol":"STOML3","gene_name":"stomatin like 3 [Source:HGNC Symbol;Acc:HGNC:19420]","synonyms":"SRO,Epb7.2l","biotype":"protein_coding","ncbi_id":"161003","summary":null,"start":38965925,"end":38991066,"strand":-1,"description":"stomatin like 3 [Source:HGNC Symbol;Acc:HGNC:19420]"}, {"versioned_ensembl_gene_id":"ENSG00000132676.15","gene_symbol":"DAP3","gene_name":"death associated protein 3 [Source:HGNC Symbol;Acc:HGNC:2673]","synonyms":"MRPS29,MRP-S29,MGC126059,MGC126058,DKFZp686G12159,DAP-3,bMRP-10","biotype":"protein_coding","ncbi_id":"7818","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that also participates in apoptotic pathways which are initiated by tumor necrosis factor-alpha, Fas ligand, and gamma interferon. This protein potentially binds ATP/GTP and might be a functional partner of the mitoribosomal protein S27. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Dec 2010]","start":155687960,"end":155739010,"strand":1,"description":"death associated protein 3 [Source:HGNC Symbol;Acc:HGNC:2673]"}, {"versioned_ensembl_gene_id":"ENSG00000283041.1","gene_symbol":"AC008038.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133034607,"end":133035920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229204.3","gene_symbol":"PTGES3P3","gene_name":"prostaglandin E synthase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43823]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441050","summary":null,"start":169791221,"end":169791702,"strand":-1,"description":"prostaglandin E synthase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43823]"}, {"versioned_ensembl_gene_id":"ENSG00000228051.1","gene_symbol":"AL512504.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80560146,"end":80562054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282217.1","gene_symbol":"AC006449.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38401836,"end":38403488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276725.4","gene_symbol":"CEP170","gene_name":"centrosomal protein 170 [Source:HGNC Symbol;Acc:HGNC:28920]","synonyms":"KIAA0470,KAB,FAM68A","biotype":"protein_coding","ncbi_id":"9859","summary":"The product of this gene is a component of the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. During interphase, the encoded protein localizes to the sub-distal appendages of mature centrioles, which are microtubule-based structures thought to help organize centrosomes. During mitosis, the protein associates with spindle microtubules near the centrosomes. The protein interacts with and is phosphorylated by polo-like kinase 1, and functions in maintaining microtubule organization and cell morphology. The human genome contains a putative transcribed pseudogene. Several alternatively spliced transcript variants of this gene have been found, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":243124428,"end":243255321,"strand":-1,"description":"centrosomal protein 170 [Source:HGNC Symbol;Acc:HGNC:28920]"}, {"versioned_ensembl_gene_id":"ENSG00000169214.4","gene_symbol":"OR6F1","gene_name":"olfactory receptor family 6 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:15027]","synonyms":"OST731","biotype":"protein_coding","ncbi_id":"343169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247711436,"end":247716646,"strand":-1,"description":"olfactory receptor family 6 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:15027]"}, {"versioned_ensembl_gene_id":"ENSG00000255801.1","gene_symbol":"AC092746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8548361,"end":8567613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228360.1","gene_symbol":"AC009220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139227537,"end":139227828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239395.2","gene_symbol":"AC118470.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":247711813,"end":247723764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237939.1","gene_symbol":"AC097523.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138307319,"end":138307970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225881.1","gene_symbol":"AC009365.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132758970,"end":132760632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268593.3","gene_symbol":"AC008749.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55707550,"end":55707855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196204.11","gene_symbol":"RNF216P1","gene_name":"ring finger protein 216 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33610]","synonyms":"RNF216L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441191","summary":null,"start":4973988,"end":5040675,"strand":1,"description":"ring finger protein 216 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33610]"}, {"versioned_ensembl_gene_id":"ENSG00000278809.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850485,"end":54867216,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000225635.7","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31803320,"end":31806899,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000261014.1","gene_symbol":"LINC02165","gene_name":"long intergenic non-protein coding RNA 2165 [Source:HGNC Symbol;Acc:HGNC:53026]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927629","summary":null,"start":63730277,"end":63754757,"strand":1,"description":"long intergenic non-protein coding RNA 2165 [Source:HGNC Symbol;Acc:HGNC:53026]"}, {"versioned_ensembl_gene_id":"ENSG00000272968.5","gene_symbol":"RBAK-RBAKDN","gene_name":"RBAK-RBAKDN readthrough [Source:HGNC Symbol;Acc:HGNC:42971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533952","summary":"This locus represents naturally occurring read-through transcription between the neighboring RBAK (RB-associated KRAB zinc finger) and LOC389458 (hypothetical LOC389458) genes on chromosome 7. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to frameshifts relative to the downstream gene. [provided by RefSeq, Mar 2011]","start":4983718,"end":5073221,"strand":1,"description":"RBAK-RBAKDN readthrough [Source:HGNC Symbol;Acc:HGNC:42971]"}, {"versioned_ensembl_gene_id":"ENSG00000117000.8","gene_symbol":"RLF","gene_name":"rearranged L-myc fusion [Source:HGNC Symbol;Acc:HGNC:10025]","synonyms":"ZNF292L,Zn-15L","biotype":"protein_coding","ncbi_id":"6018","summary":null,"start":40161373,"end":40240921,"strand":1,"description":"rearranged L-myc fusion [Source:HGNC Symbol;Acc:HGNC:10025]"}, {"versioned_ensembl_gene_id":"ENSG00000259864.1","gene_symbol":"AC018846.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63703483,"end":63703665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275328.1","gene_symbol":"SPDYE19P","gene_name":"speedy/RINGO cell cycle regulator family member E19, pseudogene [Source:HGNC Symbol;Acc:HGNC:51515]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130307","summary":null,"start":5031608,"end":5037831,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E19, pseudogene [Source:HGNC Symbol;Acc:HGNC:51515]"}, {"versioned_ensembl_gene_id":"ENSG00000274827.4","gene_symbol":"LINC01297","gene_name":"long intergenic non-protein coding RNA 1297 [Source:HGNC Symbol;Acc:HGNC:50443]","synonyms":"LA16c-83F12.6","biotype":"lincRNA","ncbi_id":"106146148","summary":null,"start":19344578,"end":19384587,"strand":-1,"description":"long intergenic non-protein coding RNA 1297 [Source:HGNC Symbol;Acc:HGNC:50443]"}, {"versioned_ensembl_gene_id":"ENSG00000278301.1","gene_symbol":"GRAMD4P3","gene_name":"GRAM domain containing 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49138]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631248","summary":null,"start":19371822,"end":19373490,"strand":1,"description":"GRAM domain containing 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49138]"}, {"versioned_ensembl_gene_id":"ENSG00000224646.2","gene_symbol":"AC007387.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74754670,"end":74754819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185792.9","gene_symbol":"NLRP9","gene_name":"NLR family pyrin domain containing 9 [Source:HGNC Symbol;Acc:HGNC:22941]","synonyms":"PAN12,NOD6,NALP9,CLR19.1","biotype":"protein_coding","ncbi_id":"338321","summary":"The protein encoded by this gene belongs to the NALP protein family. Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). This protein may play a regulatory role in the innate immune system as similar family members belong to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. [provided by RefSeq, Jul 2008]","start":55708432,"end":55738402,"strand":-1,"description":"NLR family pyrin domain containing 9 [Source:HGNC Symbol;Acc:HGNC:22941]"}, {"versioned_ensembl_gene_id":"ENSG00000261743.1","gene_symbol":"AC138305.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63368844,"end":63369456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241808.1","gene_symbol":"RPS15AP34","gene_name":"ribosomal protein S15a pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35609]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390735","summary":null,"start":63350763,"end":63351149,"strand":-1,"description":"ribosomal protein S15a pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35609]"}, {"versioned_ensembl_gene_id":"ENSG00000272311.1","gene_symbol":"IFNL4P1","gene_name":"interferon lambda 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45090]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927833","summary":null,"start":39264382,"end":39265817,"strand":1,"description":"interferon lambda 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45090]"}, {"versioned_ensembl_gene_id":"ENSG00000283374.1","gene_symbol":"TXNRD3NB","gene_name":"thioredoxin reductase 3 neighbor [Source:HGNC Symbol;Acc:HGNC:33870]","synonyms":"TR2IT1,TXNRD3NT1,TXNRD3IT1,TR2IT1,TXNRD3NT1,TXNRD3IT1","biotype":"protein_coding","ncbi_id":"645840","summary":null,"start":126571779,"end":126608555,"strand":-1,"description":"thioredoxin reductase 3 neighbor [Source:HGNC Symbol;Acc:HGNC:33870]"}, {"versioned_ensembl_gene_id":"ENSG00000242136.1","gene_symbol":"AC093904.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9103440,"end":9105114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234487.11","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29719887,"end":29722948,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000260658.5","gene_symbol":"AC138305.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63314264,"end":63618046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249663.1","gene_symbol":"CR759790.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720114,"end":29721104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280261.1","gene_symbol":"AC009161.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":62342420,"end":62342557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273398.6","gene_symbol":"AC017083.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":68131238,"end":68261230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183470.9","gene_symbol":"FLJ40288","gene_name":"uncharacterized FLJ40288 [Source:NCBI gene;Acc:286023]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286023","summary":null,"start":132648794,"end":132728769,"strand":1,"description":"uncharacterized FLJ40288 [Source:NCBI gene;Acc:286023]"}, {"versioned_ensembl_gene_id":"ENSG00000080503.22","gene_symbol":"SMARCA2","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 [Source:HGNC Symbol;Acc:HGNC:11098]","synonyms":"SWI2,Sth1p,SNF2LA,SNF2L2,SNF2,hSNF2a,hBRM,BRM,BAF190","biotype":"protein_coding","ncbi_id":"6595","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins and is highly similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, which contains a trinucleotide repeat (CAG) length polymorphism. [provided by RefSeq, Jan 2014]","start":1980290,"end":2193624,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 [Source:HGNC Symbol;Acc:HGNC:11098]"}, {"versioned_ensembl_gene_id":"ENSG00000163735.6","gene_symbol":"CXCL5","gene_name":"C-X-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10642]","synonyms":"SCYB5,ENA-78","biotype":"protein_coding","ncbi_id":"6374","summary":"This gene encodes a protein that is a member of the CXC subfamily of chemokines. Chemokines, which recruit and activate leukocytes, are classified by function (inflammatory or homeostatic) or by structure. This protein is proposed to bind the G-protein coupled receptor chemokine (C-X-C motif) receptor 2 to recruit neutrophils, to promote angiogenesis and to remodel connective tissues. This protein is thought to play a role in cancer cell proliferation, migration, and invasion. [provided by RefSeq, May 2013]","start":73995642,"end":73998779,"strand":-1,"description":"C-X-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10642]"}, {"versioned_ensembl_gene_id":"ENSG00000136261.14","gene_symbol":"BZW2","gene_name":"basic leucine zipper and W2 domains 2 [Source:HGNC Symbol;Acc:HGNC:18808]","synonyms":"HSPC028,MSTP017,MST017","biotype":"protein_coding","ncbi_id":"28969","summary":null,"start":16646131,"end":16706523,"strand":1,"description":"basic leucine zipper and W2 domains 2 [Source:HGNC Symbol;Acc:HGNC:18808]"}, {"versioned_ensembl_gene_id":"ENSG00000056050.6","gene_symbol":"HPF1","gene_name":"histone PARylation factor 1 [Source:HGNC Symbol;Acc:HGNC:26051]","synonyms":"FLJ20534,C4orf27","biotype":"protein_coding","ncbi_id":"54969","summary":null,"start":169729465,"end":169757953,"strand":-1,"description":"histone PARylation factor 1 [Source:HGNC Symbol;Acc:HGNC:26051]"}, {"versioned_ensembl_gene_id":"ENSG00000185158.12","gene_symbol":"LRRC37B","gene_name":"leucine rich repeat containing 37B [Source:HGNC Symbol;Acc:HGNC:29070]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114659","summary":null,"start":32007872,"end":32053504,"strand":1,"description":"leucine rich repeat containing 37B [Source:HGNC Symbol;Acc:HGNC:29070]"}, {"versioned_ensembl_gene_id":"ENSG00000264497.1","gene_symbol":"AC090616.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32024469,"end":32024583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280199.1","gene_symbol":"Z82202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49264201,"end":49266080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250210.5","gene_symbol":"FO082796.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":138286248,"end":138286430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226142.2","gene_symbol":"RPL35P8","gene_name":"ribosomal protein L35 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36158]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643653","summary":null,"start":49213911,"end":49214247,"strand":-1,"description":"ribosomal protein L35 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36158]"}, {"versioned_ensembl_gene_id":"ENSG00000266777.1","gene_symbol":"AC090616.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32039974,"end":32042828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236199.1","gene_symbol":"AL359076.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2041900,"end":2046023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240898.1","gene_symbol":"AC132942.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3665220,"end":3665702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272345.1","gene_symbol":"AL031775.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24700907,"end":24701793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262903.1","gene_symbol":"AC027796.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3655621,"end":3658092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010327.10","gene_symbol":"STAB1","gene_name":"stabilin 1 [Source:HGNC Symbol;Acc:HGNC:18628]","synonyms":"STAB-1,SCARH2,KIAA0246,FEX1,FELE-1,FEEL-1,CLEVER-1","biotype":"protein_coding","ncbi_id":"23166","summary":"This gene encodes a large, transmembrane receptor protein which may function in angiogenesis, lymphocyte homing, cell adhesion, or receptor scavenging. The protein contains 7 fasciclin, 16 epidermal growth factor (EGF)-like, and 2 laminin-type EGF-like domains as well as a C-type lectin-like hyaluronan-binding Link module. The protein is primarily expressed on sinusoidal endothelial cells of liver, spleen, and lymph node. The receptor has been shown to endocytose ligands such as low density lipoprotein, Gram-positive and Gram-negative bacteria, and advanced glycosylation end products. Supporting its possible role as a scavenger receptor, the protein rapidly cycles between the plasma membrane and early endosomes. [provided by RefSeq, Jul 2008]","start":52495338,"end":52524495,"strand":1,"description":"stabilin 1 [Source:HGNC Symbol;Acc:HGNC:18628]"}, {"versioned_ensembl_gene_id":"ENSG00000233013.10","gene_symbol":"FAM157B","gene_name":"family with sequence similarity 157 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34080]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132403","summary":null,"start":138217068,"end":138253217,"strand":1,"description":"family with sequence similarity 157 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34080]"}, {"versioned_ensembl_gene_id":"ENSG00000204536.13","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"HCR,C6orf18","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31142439,"end":31158238,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000234958.6","gene_symbol":"FABP5P13","gene_name":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]","synonyms":"FABP5L13","biotype":"processed_pseudogene","ncbi_id":"106480712","summary":null,"start":523775,"end":524102,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]"}, {"versioned_ensembl_gene_id":"ENSG00000273443.1","gene_symbol":"AL645608.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1062208,"end":1063288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162997.15","gene_symbol":"PRORSD1P","gene_name":"prolyl-tRNA synthetase associated domain containing 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:34379]","synonyms":"Ybakd1,PRDXDD1P,Prdxdd1,NCRNA00117","biotype":"transcribed_unitary_pseudogene","ncbi_id":"344405","summary":null,"start":55282319,"end":55284522,"strand":1,"description":"prolyl-tRNA synthetase associated domain containing 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:34379]"}, {"versioned_ensembl_gene_id":"ENSG00000159958.6","gene_symbol":"TNFRSF13C","gene_name":"TNF receptor superfamily member 13C [Source:HGNC Symbol;Acc:HGNC:17755]","synonyms":"CD268,BAFFR","biotype":"protein_coding","ncbi_id":"115650","summary":"B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008]","start":41922023,"end":41926818,"strand":-1,"description":"TNF receptor superfamily member 13C [Source:HGNC Symbol;Acc:HGNC:17755]"}, {"versioned_ensembl_gene_id":"ENSG00000230314.6","gene_symbol":"ELOVL2-AS1","gene_name":"ELOVL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44156]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506409","summary":null,"start":11043524,"end":11078226,"strand":1,"description":"ELOVL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44156]"}, {"versioned_ensembl_gene_id":"ENSG00000271629.1","gene_symbol":"AC067959.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21198518,"end":21198896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234965.2","gene_symbol":"SHISA8","gene_name":"shisa family member 8 [Source:HGNC Symbol;Acc:HGNC:18351]","synonyms":"Orf26,C22orf17","biotype":"protein_coding","ncbi_id":"440829","summary":null,"start":41909554,"end":41914667,"strand":-1,"description":"shisa family member 8 [Source:HGNC Symbol;Acc:HGNC:18351]"}, {"versioned_ensembl_gene_id":"ENSG00000197437.4","gene_symbol":"OR13G1","gene_name":"olfactory receptor family 13 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:14999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441933","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247670812,"end":247679739,"strand":-1,"description":"olfactory receptor family 13 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:14999]"}, {"versioned_ensembl_gene_id":"ENSG00000226417.6","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"NCC27,G6,p64CLCP","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31806863,"end":31816046,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000163736.3","gene_symbol":"PPBP","gene_name":"pro-platelet basic protein [Source:HGNC Symbol;Acc:HGNC:9240]","synonyms":"THBGB1,TGB1,TGB,SCYB7,PBP,NAP-2-L1,NAP-2,MDGF,LDGF,LA-PF4,CXCL7,CTAPIII,CTAP3,Beta-TG,b-TG1","biotype":"protein_coding","ncbi_id":"5473","summary":"The protein encoded by this gene is a platelet-derived growth factor that belongs to the CXC chemokine family. This growth factor is a potent chemoattractant and activator of neutrophils. It has been shown to stimulate various cellular processes including DNA synthesis, mitosis, glycolysis, intracellular cAMP accumulation, prostaglandin E2 secretion, and synthesis of hyaluronic acid and sulfated glycosaminoglycan. It also stimulates the formation and secretion of plasminogen activator by synovial cells. The protein also is an antimicrobial protein with bactericidal and antifungal activity. [provided by RefSeq, Nov 2014]","start":73987038,"end":73988197,"strand":-1,"description":"pro-platelet basic protein [Source:HGNC Symbol;Acc:HGNC:9240]"}, {"versioned_ensembl_gene_id":"ENSG00000204399.3","gene_symbol":"AC012306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127931327,"end":127931440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272667.1","gene_symbol":"AC012306.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127886556,"end":127887185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000036054.12","gene_symbol":"TBC1D23","gene_name":"TBC1 domain family member 23 [Source:HGNC Symbol;Acc:HGNC:25622]","synonyms":"FLJ11046","biotype":"protein_coding","ncbi_id":"55773","summary":null,"start":100261000,"end":100325251,"strand":1,"description":"TBC1 domain family member 23 [Source:HGNC Symbol;Acc:HGNC:25622]"}, {"versioned_ensembl_gene_id":"ENSG00000164690.7","gene_symbol":"SHH","gene_name":"sonic hedgehog [Source:HGNC Symbol;Acc:HGNC:10848]","synonyms":"HLP3,HHG1,TPTPS,TPT,SMMCI,MCOPCB5,HPE3","biotype":"protein_coding","ncbi_id":"6469","summary":"This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly. [provided by RefSeq, Jul 2008]","start":155799986,"end":155812273,"strand":-1,"description":"sonic hedgehog [Source:HGNC Symbol;Acc:HGNC:10848]"}, {"versioned_ensembl_gene_id":"ENSG00000100099.20","gene_symbol":"HPS4","gene_name":"HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 [Source:HGNC Symbol;Acc:HGNC:15844]","synonyms":"LE,KIAA1667,BLOC3S2","biotype":"protein_coding","ncbi_id":"89781","summary":"This gene encodes a protein component of biogenesis of lysosome-related organelles complexes (BLOC). BLOC complexes are important for the formation of endosomal-lysosomal organelles such as melanosomes and platelet dense granules. Mutations in this gene result in subtype 4 of Hermansky-Pudlak syndrome, a form of albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":26443423,"end":26483837,"strand":-1,"description":"HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 [Source:HGNC Symbol;Acc:HGNC:15844]"}, {"versioned_ensembl_gene_id":"ENSG00000235058.1","gene_symbol":"ZMYND10-AS1","gene_name":"ZMYND10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40890]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874210","summary":null,"start":50341106,"end":50345697,"strand":1,"description":"ZMYND10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40890]"}, {"versioned_ensembl_gene_id":"ENSG00000251615.3","gene_symbol":"AC104825.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8355090,"end":8358338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128203.6","gene_symbol":"ASPHD2","gene_name":"aspartate beta-hydroxylase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30437]","synonyms":"FLJ39838","biotype":"protein_coding","ncbi_id":"57168","summary":null,"start":26429273,"end":26445015,"strand":1,"description":"aspartate beta-hydroxylase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30437]"}, {"versioned_ensembl_gene_id":"ENSG00000281849.3","gene_symbol":"AL732314.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":386980,"end":405579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244310.1","gene_symbol":"AC093904.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9115197,"end":9116884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261104.1","gene_symbol":"AC093904.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9106593,"end":9109865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223640.1","gene_symbol":"RPL30P3","gene_name":"ribosomal protein L30 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270977","summary":null,"start":9081395,"end":9081727,"strand":-1,"description":"ribosomal protein L30 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36380]"}, {"versioned_ensembl_gene_id":"ENSG00000281976.1","gene_symbol":"ADAMTS7P1","gene_name":"ADAMTS7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49407]","synonyms":"ADAMTS7P2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390660","summary":null,"start":82298559,"end":82334628,"strand":1,"description":"ADAMTS7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49407]"}, {"versioned_ensembl_gene_id":"ENSG00000226564.1","gene_symbol":"FTH1P20","gene_name":"ferritin heavy chain 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37639]","synonyms":"FTHL20","biotype":"processed_pseudogene","ncbi_id":"729009","summary":null,"start":180872867,"end":180873414,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37639]"}, {"versioned_ensembl_gene_id":"ENSG00000280390.1","gene_symbol":"AC010872.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21023496,"end":21024170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237385.1","gene_symbol":"AL583839.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93430342,"end":93431299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231666.6","gene_symbol":"LINC01704","gene_name":"long intergenic non-protein coding RNA 1704 [Source:HGNC Symbol;Acc:HGNC:52492]","synonyms":null,"biotype":"lincRNA","ncbi_id":"646268","summary":null,"start":158132040,"end":158146929,"strand":-1,"description":"long intergenic non-protein coding RNA 1704 [Source:HGNC Symbol;Acc:HGNC:52492]"}, {"versioned_ensembl_gene_id":"ENSG00000182545.6","gene_symbol":"RNASE10","gene_name":"ribonuclease A family member 10 (inactive) [Source:HGNC Symbol;Acc:HGNC:19275]","synonyms":"RNASE9,RAH1","biotype":"protein_coding","ncbi_id":"338879","summary":null,"start":20505537,"end":20511169,"strand":1,"description":"ribonuclease A family member 10 (inactive) [Source:HGNC Symbol;Acc:HGNC:19275]"}, {"versioned_ensembl_gene_id":"ENSG00000265972.5","gene_symbol":"TXNIP","gene_name":"thioredoxin interacting protein [Source:HGNC Symbol;Acc:HGNC:16952]","synonyms":"THIF,HHCPA78,EST01027,ARRDC6,VDUP1","biotype":"protein_coding","ncbi_id":"10628","summary":"This gene encodes a thioredoxin-binding protein that is a member of the alpha arrestin protein family. Thioredoxin is a thiol-oxidoreductase that is a major regulator of cellular redox signaling which protects cells from oxidative stress. This protein inhibits the antioxidative function of thioredoxin resulting in the accumulation of reactive oxygen species and cellular stress. This protein also functions as a regulator of cellular metabolism and of endoplasmic reticulum (ER) stress. This protein may also function as a tumor suppressor. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":145992435,"end":145996600,"strand":-1,"description":"thioredoxin interacting protein [Source:HGNC Symbol;Acc:HGNC:16952]"}, {"versioned_ensembl_gene_id":"ENSG00000227295.2","gene_symbol":"ELL2P1","gene_name":"elongation factor for RNA polymerase II 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646270","summary":null,"start":158175850,"end":158177755,"strand":-1,"description":"elongation factor for RNA polymerase II 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39343]"}, {"versioned_ensembl_gene_id":"ENSG00000258456.2","gene_symbol":"PTCD2P1","gene_name":"pentatricopeptide repeat domain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131302","summary":null,"start":20524287,"end":20525422,"strand":-1,"description":"pentatricopeptide repeat domain 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31718]"}, {"versioned_ensembl_gene_id":"ENSG00000134905.16","gene_symbol":"CARS2","gene_name":"cysteinyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:25695]","synonyms":"FLJ12118","biotype":"protein_coding","ncbi_id":"79587","summary":"This gene encodes a putative member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of cysteine to tRNA molecules. A splice-site mutation in this gene has been associated with a novel progressive myoclonic epilepsy disease with similar symptoms to MERRF syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2017]","start":110641412,"end":110713603,"strand":-1,"description":"cysteinyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:25695]"}, {"versioned_ensembl_gene_id":"ENSG00000273605.1","gene_symbol":"AC209234.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79384784,"end":79385673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234791.1","gene_symbol":"AC108448.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3189546,"end":3189929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158473.6","gene_symbol":"CD1D","gene_name":"CD1d molecule [Source:HGNC Symbol;Acc:HGNC:1637]","synonyms":null,"biotype":"protein_coding","ncbi_id":"912","summary":"This gene encodes a divergent member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":158179947,"end":158184896,"strand":1,"description":"CD1d molecule [Source:HGNC Symbol;Acc:HGNC:1637]"}, {"versioned_ensembl_gene_id":"ENSG00000281759.1","gene_symbol":"AC145029.2","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":90245744,"end":90246220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276388.1","gene_symbol":"AL591424.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":138129399,"end":138129526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268189.2","gene_symbol":"AC005785.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":15379076,"end":15381194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236301.5","gene_symbol":"MRGPRG-AS1","gene_name":"MRGPRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26691]","synonyms":"HSD-40,FLJ36102,C11orf36","biotype":"antisense_RNA","ncbi_id":"283303","summary":null,"start":3218332,"end":3223131,"strand":1,"description":"MRGPRG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26691]"}, {"versioned_ensembl_gene_id":"ENSG00000229926.1","gene_symbol":"AL591424.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":138137095,"end":138143864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279716.1","gene_symbol":"AC006128.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15398696,"end":15400356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279203.1","gene_symbol":"AC005785.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15383202,"end":15383832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182170.3","gene_symbol":"MRGPRG","gene_name":"MAS related GPR family member G [Source:HGNC Symbol;Acc:HGNC:24829]","synonyms":"mrgG,GPR169","biotype":"protein_coding","ncbi_id":"386746","summary":null,"start":3217944,"end":3218813,"strand":-1,"description":"MAS related GPR family member G [Source:HGNC Symbol;Acc:HGNC:24829]"}, {"versioned_ensembl_gene_id":"ENSG00000281925.1","gene_symbol":"AC243902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29374919,"end":29376383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011243.17","gene_symbol":"AKAP8L","gene_name":"A-kinase anchoring protein 8 like [Source:HGNC Symbol;Acc:HGNC:29857]","synonyms":"NAKAP95,HAP95","biotype":"protein_coding","ncbi_id":"26993","summary":null,"start":15380048,"end":15419141,"strand":-1,"description":"A-kinase anchoring protein 8 like [Source:HGNC Symbol;Acc:HGNC:29857]"}, {"versioned_ensembl_gene_id":"ENSG00000282130.1","gene_symbol":"NSMCE3","gene_name":"NSE3 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:7677]","synonyms":"NSE3,NDNL2,MAGEL3,MAGEG1,HCA4","biotype":"protein_coding","ncbi_id":"56160","summary":"The protein encoded by this gene is part of the SMC5-6 chromatin reorganizing complex and is a member of the MAGE superfamily. This is an intronless gene. [provided by RefSeq, May 2011]","start":29409413,"end":29411093,"strand":-1,"description":"NSE3 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:7677]"}, {"versioned_ensembl_gene_id":"ENSG00000224513.2","gene_symbol":"AC109309.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3226061,"end":3232838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273564.2","gene_symbol":"FAM189A1","gene_name":"family with sequence similarity 189 member A1 [Source:HGNC Symbol;Acc:HGNC:29075]","synonyms":"TMEM228,KIAA0574","biotype":"protein_coding","ncbi_id":"23359","summary":null,"start":29260596,"end":29720617,"strand":-1,"description":"family with sequence similarity 189 member A1 [Source:HGNC Symbol;Acc:HGNC:29075]"}, {"versioned_ensembl_gene_id":"ENSG00000184350.9","gene_symbol":"MRGPRE","gene_name":"MAS related GPR family member E [Source:HGNC Symbol;Acc:HGNC:30694]","synonyms":"mrgE,GPR167","biotype":"protein_coding","ncbi_id":"116534","summary":null,"start":3227698,"end":3232386,"strand":-1,"description":"MAS related GPR family member E [Source:HGNC Symbol;Acc:HGNC:30694]"}, {"versioned_ensembl_gene_id":"ENSG00000159247.13","gene_symbol":"TUBBP5","gene_name":"tubulin beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23674]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643224","summary":null,"start":138150075,"end":138177433,"strand":1,"description":"tubulin beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23674]"}, {"versioned_ensembl_gene_id":"ENSG00000258863.1","gene_symbol":"SETP1","gene_name":"SET pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19279]","synonyms":"SETP,SETP19","biotype":"processed_pseudogene","ncbi_id":"100133314","summary":null,"start":20528115,"end":20528959,"strand":-1,"description":"SET pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19279]"}, {"versioned_ensembl_gene_id":"ENSG00000236987.2","gene_symbol":"NDUFA5P8","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48850]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"103091863","summary":null,"start":3276045,"end":3276390,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48850]"}, {"versioned_ensembl_gene_id":"ENSG00000204603.6","gene_symbol":"LINC01257","gene_name":"long intergenic non-protein coding RNA 1257 [Source:HGNC Symbol;Acc:HGNC:26972]","synonyms":null,"biotype":"lincRNA","ncbi_id":"116437","summary":null,"start":131165011,"end":131212931,"strand":1,"description":"long intergenic non-protein coding RNA 1257 [Source:HGNC Symbol;Acc:HGNC:26972]"}, {"versioned_ensembl_gene_id":"ENSG00000276951.1","gene_symbol":"AC109309.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3289311,"end":3289642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232390.3","gene_symbol":"NDUFA5P1","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7689]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"4699","summary":null,"start":3321862,"end":3322202,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7689]"}, {"versioned_ensembl_gene_id":"ENSG00000230324.1","gene_symbol":"LINC01734","gene_name":"long intergenic non-protein coding RNA 1734 [Source:HGNC Symbol;Acc:HGNC:52522]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339568","summary":null,"start":39213777,"end":39224748,"strand":-1,"description":"long intergenic non-protein coding RNA 1734 [Source:HGNC Symbol;Acc:HGNC:52522]"}, {"versioned_ensembl_gene_id":"ENSG00000089775.11","gene_symbol":"ZBTB25","gene_name":"zinc finger and BTB domain containing 25 [Source:HGNC Symbol;Acc:HGNC:13112]","synonyms":"ZNF46,KUP,C14orf51","biotype":"protein_coding","ncbi_id":"7597","summary":null,"start":64449106,"end":64505213,"strand":-1,"description":"zinc finger and BTB domain containing 25 [Source:HGNC Symbol;Acc:HGNC:13112]"}, {"versioned_ensembl_gene_id":"ENSG00000280217.1","gene_symbol":"AC126564.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131235511,"end":131237523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121957.12","gene_symbol":"GPSM2","gene_name":"G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29501]","synonyms":"Pins,LGN,DFNB82","biotype":"protein_coding","ncbi_id":"29899","summary":"The protein encoded by this gene belongs to a family of proteins that modulate activation of G proteins, which transduce extracellular signals received by cell surface receptors into integrated cellular responses. The N-terminal half of this protein contains 10 copies of leu-gly-asn (LGN) repeat, and the C-terminal half contains 4 GoLoco motifs, which are involved in guanine nucleotide exchange. This protein may play a role in neuroblast division and in the development of normal hearing. Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":108875350,"end":108934545,"strand":1,"description":"G protein signaling modulator 2 [Source:HGNC Symbol;Acc:HGNC:29501]"}, {"versioned_ensembl_gene_id":"ENSG00000229914.1","gene_symbol":"AL138899.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158195633,"end":158196131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273813.1","gene_symbol":"AC123788.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3335125,"end":3335407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282503.1","gene_symbol":"AC243686.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29514804,"end":29518158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278130.1","gene_symbol":"AL591424.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":138177426,"end":138179774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278697.1","gene_symbol":"AL078601.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79354443,"end":79354713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226179.6","gene_symbol":"LINC00685","gene_name":"long intergenic non-protein coding RNA 685 [Source:HGNC Symbol;Acc:HGNC:27560]","synonyms":"PPP2R3B-AS1,OTTHUMT00000055574,NCRNA00107,CXYorf10","biotype":"antisense_RNA","ncbi_id":"283981","summary":null,"start":320990,"end":321851,"strand":1,"description":"long intergenic non-protein coding RNA 685 [Source:HGNC Symbol;Acc:HGNC:27560]"}, {"versioned_ensembl_gene_id":"ENSG00000126803.9","gene_symbol":"HSPA2","gene_name":"heat shock protein family A (Hsp70) member 2 [Source:HGNC Symbol;Acc:HGNC:5235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3306","summary":null,"start":64535905,"end":64546173,"strand":1,"description":"heat shock protein family A (Hsp70) member 2 [Source:HGNC Symbol;Acc:HGNC:5235]"}, {"versioned_ensembl_gene_id":"ENSG00000083454.21","gene_symbol":"P2RX5","gene_name":"purinergic receptor P2X 5 [Source:HGNC Symbol;Acc:HGNC:8536]","synonyms":"P2X5,LRH-1","biotype":"protein_coding","ncbi_id":"5026","summary":"The product of this gene belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring downstream gene, TAX1BP3 (Tax1 binding protein 3). [provided by RefSeq, Mar 2011]","start":3672199,"end":3696404,"strand":-1,"description":"purinergic receptor P2X 5 [Source:HGNC Symbol;Acc:HGNC:8536]"}, {"versioned_ensembl_gene_id":"ENSG00000112697.15","gene_symbol":"TMEM30A","gene_name":"transmembrane protein 30A [Source:HGNC Symbol;Acc:HGNC:16667]","synonyms":"C6orf67,FLJ10856,CDC50A","biotype":"protein_coding","ncbi_id":"55754","summary":null,"start":75252924,"end":75284968,"strand":-1,"description":"transmembrane protein 30A [Source:HGNC Symbol;Acc:HGNC:16667]"}, {"versioned_ensembl_gene_id":"ENSG00000215580.10","gene_symbol":"BCORP1","gene_name":"BCL6 corepressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23953]","synonyms":"BCORL2,FLJ39821","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"286554","summary":null,"start":19455431,"end":19503153,"strand":-1,"description":"BCL6 corepressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23953]"}, {"versioned_ensembl_gene_id":"ENSG00000231377.6","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DDX16,PRPF2,DBP2,Prp2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30731576,"end":30751521,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000259160.1","gene_symbol":"AL049869.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64535702,"end":64535879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250412.1","gene_symbol":"KLHL2P1","gene_name":"kelch like family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44046]","synonyms":"MAVP1","biotype":"unprocessed_pseudogene","ncbi_id":"729249","summary":null,"start":119334329,"end":119378233,"strand":1,"description":"kelch like family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44046]"}, {"versioned_ensembl_gene_id":"ENSG00000179841.8","gene_symbol":"AKAP5","gene_name":"A-kinase anchoring protein 5 [Source:HGNC Symbol;Acc:HGNC:375]","synonyms":"AKAP79,AKAP75","biotype":"protein_coding","ncbi_id":"9495","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein binds to the RII-beta regulatory subunit of PKA, and also to protein kinase C and the phosphatase calcineurin. It is predominantly expressed in cerebral cortex and may anchor the PKA protein at postsynaptic densities (PSD) and be involved in the regulation of postsynaptic events. It is also expressed in T lymphocytes and may function to inhibit interleukin-2 transcription by disrupting calcineurin-dependent dephosphorylation of NFAT. [provided by RefSeq, Jul 2008]","start":64465499,"end":64474503,"strand":1,"description":"A-kinase anchoring protein 5 [Source:HGNC Symbol;Acc:HGNC:375]"}, {"versioned_ensembl_gene_id":"ENSG00000275777.3","gene_symbol":"IGKV3D-7","gene_name":"immunoglobulin kappa variable 3D-7 [Source:HGNC Symbol;Acc:HGNC:5829]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28877","summary":null,"start":90259509,"end":90260067,"strand":1,"description":"immunoglobulin kappa variable 3D-7 [Source:HGNC Symbol;Acc:HGNC:5829]"}, {"versioned_ensembl_gene_id":"ENSG00000176753.5","gene_symbol":"C15orf56","gene_name":"chromosome 15 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:33868]","synonyms":"FLJ38596","biotype":"processed_transcript","ncbi_id":"644809","summary":null,"start":40250664,"end":40252969,"strand":-1,"description":"chromosome 15 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:33868]"}, {"versioned_ensembl_gene_id":"ENSG00000163510.13","gene_symbol":"CWC22","gene_name":"CWC22 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:29322]","synonyms":"NCM,KIAA1604,fSAPb,EIF4GL","biotype":"protein_coding","ncbi_id":"57703","summary":null,"start":179944876,"end":180007113,"strand":-1,"description":"CWC22 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:29322]"}, {"versioned_ensembl_gene_id":"ENSG00000272909.1","gene_symbol":"AL122035.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64440369,"end":64442238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113645.14","gene_symbol":"WWC1","gene_name":"WW and C2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29435]","synonyms":"KIAA0869,PPP1R168,KIBRA","biotype":"protein_coding","ncbi_id":"23286","summary":"The protein encoded by this gene is a cytoplasmic phosphoprotein that interacts with PRKC-zeta and dynein light chain-1. Alleles of this gene have been found that enhance memory in some individuals. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":168291651,"end":168472303,"strand":1,"description":"WW and C2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29435]"}, {"versioned_ensembl_gene_id":"ENSG00000281421.1","gene_symbol":"AL513210.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":168820423,"end":168820656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259116.1","gene_symbol":"AL049869.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64514154,"end":64540368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273786.1","gene_symbol":"AC020658.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40226386,"end":40227069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280768.1","gene_symbol":"AC145029.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90340444,"end":90340547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260648.3","gene_symbol":"AC020658.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40232082,"end":40236109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281625.1","gene_symbol":"AL354892.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169725091,"end":169725854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264300.1","gene_symbol":"AC090616.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32003110,"end":32006688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279409.1","gene_symbol":"AC020658.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40258501,"end":40260370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281410.1","gene_symbol":"AL354892.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169725504,"end":169738992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137843.11","gene_symbol":"PAK6","gene_name":"p21 (RAC1) activated kinase 6 [Source:HGNC Symbol;Acc:HGNC:16061]","synonyms":"PAK5","biotype":"protein_coding","ncbi_id":"56924","summary":"This gene encodes a member of a family of p21-stimulated serine/threonine protein kinases, which contain an amino-terminal Cdc42/Rac interactive binding (CRIB) domain and a carboxyl-terminal kinase domain. These kinases function in a number of cellular processes, including cytoskeleton rearrangement, apoptosis, and the mitogen-activated protein (MAP) kinase signaling pathway. The protein encoded by this gene interacts with androgen receptor (AR) and translocates to the nucleus, where it is involved in transcriptional regulation. Changes in expression of this gene have been linked to prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":40238759,"end":40277487,"strand":1,"description":"p21 (RAC1) activated kinase 6 [Source:HGNC Symbol;Acc:HGNC:16061]"}, {"versioned_ensembl_gene_id":"ENSG00000280572.1","gene_symbol":"IGKV1OR2-118","gene_name":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]","synonyms":"IGKV1/OR2-118","biotype":"IG_V_pseudogene","ncbi_id":"339562","summary":null,"start":90346572,"end":90347042,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]"}, {"versioned_ensembl_gene_id":"ENSG00000163352.5","gene_symbol":"LENEP","gene_name":"lens epithelial protein [Source:HGNC Symbol;Acc:HGNC:14429]","synonyms":"LEP503","biotype":"protein_coding","ncbi_id":"55891","summary":"The ocular lens is a tissue of epithelial origin and devoid of blood vessels and nerves. Cells of the lens epithelium are responsible for the growth and maintenance of the lens through mitosis, protein synthesis, and active transport of ions and metabolites across the lens capsule. Lens epithelial protein is expressed exclusively in lens epithelial cells and may play a role in cell differentiation. [provided by RefSeq, Jul 2008]","start":154993586,"end":154994315,"strand":1,"description":"lens epithelial protein [Source:HGNC Symbol;Acc:HGNC:14429]"}, {"versioned_ensembl_gene_id":"ENSG00000280569.1","gene_symbol":"AC233263.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90389792,"end":90390015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188505.4","gene_symbol":"NCCRP1","gene_name":"non-specific cytotoxic cell receptor protein 1 homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:33739]","synonyms":"LOC342897,FBXO50,NCCRP-1","biotype":"protein_coding","ncbi_id":"342897","summary":null,"start":39196961,"end":39201884,"strand":1,"description":"non-specific cytotoxic cell receptor protein 1 homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:33739]"}, {"versioned_ensembl_gene_id":"ENSG00000280491.1","gene_symbol":"AC233263.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90395720,"end":90397682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235190.1","gene_symbol":"AL008629.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131937670,"end":131937853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271267.1","gene_symbol":"AL353807.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155566050,"end":155566306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235363.1","gene_symbol":"SNRPGP10","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130289","summary":null,"start":205351247,"end":205351471,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39329]"}, {"versioned_ensembl_gene_id":"ENSG00000162873.14","gene_symbol":"KLHDC8A","gene_name":"kelch domain containing 8A [Source:HGNC Symbol;Acc:HGNC:25573]","synonyms":"FLJ10748","biotype":"protein_coding","ncbi_id":"55220","summary":"This gene encodes a kelch domain-containing protein which is upregulated in cancer. Upregulated expression of the encoded protein may provide an alternative pathway for tumors to maintain aggressiveness in the absence of epidermal growth factor receptor dependence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":205336065,"end":205357090,"strand":-1,"description":"kelch domain containing 8A [Source:HGNC Symbol;Acc:HGNC:25573]"}, {"versioned_ensembl_gene_id":"ENSG00000273320.1","gene_symbol":"AC007032.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106285480,"end":106286326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223858.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672173,"end":29680888,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000105835.11","gene_symbol":"NAMPT","gene_name":"nicotinamide phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30092]","synonyms":"PBEF1,PBEF","biotype":"protein_coding","ncbi_id":"10135","summary":"This gene encodes a protein that catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to yield nicotinamide mononucleotide, one step in the biosynthesis of nicotinamide adenine dinucleotide. The protein belongs to the nicotinic acid phosphoribosyltransferase (NAPRTase) family and is thought to be involved in many important biological processes, including metabolism, stress response and aging. This gene has a pseudogene on chromosome 10. [provided by RefSeq, Feb 2011]","start":106248285,"end":106286326,"strand":-1,"description":"nicotinamide phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30092]"}, {"versioned_ensembl_gene_id":"ENSG00000179751.6","gene_symbol":"SYCN","gene_name":"syncollin [Source:HGNC Symbol;Acc:HGNC:18442]","synonyms":"FLJ27441,SYL,INSSA1","biotype":"protein_coding","ncbi_id":"342898","summary":null,"start":39202831,"end":39204266,"strand":-1,"description":"syncollin [Source:HGNC Symbol;Acc:HGNC:18442]"}, {"versioned_ensembl_gene_id":"ENSG00000258057.5","gene_symbol":"BCDIN3D-AS1","gene_name":"BCDIN3D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44113]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100286844","summary":null,"start":49828542,"end":49841143,"strand":1,"description":"BCDIN3D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44113]"}, {"versioned_ensembl_gene_id":"ENSG00000227603.1","gene_symbol":"AL583839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93435332,"end":93437121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106524.8","gene_symbol":"ANKMY2","gene_name":"ankyrin repeat and MYND domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25370]","synonyms":"ZMYND20,DKFZP564O043","biotype":"protein_coding","ncbi_id":"57037","summary":null,"start":16599776,"end":16645817,"strand":-1,"description":"ankyrin repeat and MYND domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25370]"}, {"versioned_ensembl_gene_id":"ENSG00000162641.18","gene_symbol":"AKNAD1","gene_name":"AKNA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28398]","synonyms":"MGC26989,C1orf62","biotype":"protein_coding","ncbi_id":"254268","summary":"This gene encodes a protein which contains a domain found in an AT-hook-containing transcription factor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":108815898,"end":108858228,"strand":-1,"description":"AKNA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28398]"}, {"versioned_ensembl_gene_id":"ENSG00000260551.1","gene_symbol":"PWRN2","gene_name":"Prader-Willi region non-protein coding RNA 2 [Source:HGNC Symbol;Acc:HGNC:33236]","synonyms":"NCRNA00199","biotype":"lincRNA","ncbi_id":"791115","summary":null,"start":24162754,"end":24169948,"strand":-1,"description":"Prader-Willi region non-protein coding RNA 2 [Source:HGNC Symbol;Acc:HGNC:33236]"}, {"versioned_ensembl_gene_id":"ENSG00000176320.2","gene_symbol":"AL138899.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158197922,"end":158203877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260091.1","gene_symbol":"AC093752.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119409333,"end":119410233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154485.4","gene_symbol":"MMP21","gene_name":"matrix metallopeptidase 21 [Source:HGNC Symbol;Acc:HGNC:14357]","synonyms":null,"biotype":"protein_coding","ncbi_id":"118856","summary":"This gene encodes a member of the matrix metalloproteinase family. Proteins in this family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, and disease processes, such as asthma and tumor metastasis. The encoded protein may play an important role in embryogenesis, particularly in neuronal cells, as well as in lymphocyte development and survival. [provided by RefSeq, May 2013]","start":125766453,"end":125775821,"strand":-1,"description":"matrix metallopeptidase 21 [Source:HGNC Symbol;Acc:HGNC:14357]"}, {"versioned_ensembl_gene_id":"ENSG00000167393.17","gene_symbol":"PPP2R3B","gene_name":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]","synonyms":"PPP2R3L,PR70,PR48,PPP2R3LY","biotype":"protein_coding","ncbi_id":"28227","summary":"Protein phosphatase 2 (formerly named type 2A) is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phosphatase 2 holoenzymes are heterotrimeric proteins composed of a structural subunit A, a catalytic subunit C, and a regulatory subunit B. The regulatory subunit is encoded by a diverse set of genes that have been grouped into the B/PR55, B'/PR61, and B''/PR72 families. These different regulatory subunits confer distinct enzymatic specificities and intracellular localizations to the holozenzyme. The product of this gene belongs to the B'' family. The B'' family has been further divided into subfamilies. The product of this gene belongs to the beta subfamily of regulatory subunit B''. [provided by RefSeq, Apr 2010]","start":333963,"end":386955,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]"}, {"versioned_ensembl_gene_id":"ENSG00000172775.16","gene_symbol":"FAM192A","gene_name":"family with sequence similarity 192 member A [Source:HGNC Symbol;Acc:HGNC:29856]","synonyms":"NIP30,C16orf94","biotype":"protein_coding","ncbi_id":"80011","summary":null,"start":57152466,"end":57186116,"strand":-1,"description":"family with sequence similarity 192 member A [Source:HGNC Symbol;Acc:HGNC:29856]"}, {"versioned_ensembl_gene_id":"ENSG00000256915.1","gene_symbol":"AC090023.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65644334,"end":65663299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186666.5","gene_symbol":"BCDIN3D","gene_name":"BCDIN3 domain containing RNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:27050]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144233","summary":"This gene encodes an RNA methyltransferase which belongs to the rossmann fold methyltransferase family, and serves as a 5'-methylphosphate capping enzyme that is specific for cytoplasmic histidyl tRNA. The encoded protein contains an S-adenosylmethionine binding domain and uses the methyl group donor, S-adenosylmethionine. This gene is overexpressed in breast cancer cells, and is related to the tumorigenic phenotype and poor prognosis of breast cancer. The encoded protein is thought to promote the cellular invasion of breast cancer cells, by downregulating the expression of tumor suppressor miRNAs through the dimethylation of the 5-monophosphate of the corresponding precursor miRNAs. [provided by RefSeq, Apr 2017]","start":49836039,"end":49843129,"strand":-1,"description":"BCDIN3 domain containing RNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:27050]"}, {"versioned_ensembl_gene_id":"ENSG00000213344.2","gene_symbol":"PCNPP3","gene_name":"PEST containing nuclear protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41975]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729298","summary":null,"start":65645992,"end":65646462,"strand":-1,"description":"PEST containing nuclear protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41975]"}, {"versioned_ensembl_gene_id":"ENSG00000273209.1","gene_symbol":"AC069148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":202032770,"end":202033537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130787.13","gene_symbol":"HIP1R","gene_name":"huntingtin interacting protein 1 related [Source:HGNC Symbol;Acc:HGNC:18415]","synonyms":"KIAA0655,ILWEQ,HIP3,HIP12,FLJ14000","biotype":"protein_coding","ncbi_id":"9026","summary":null,"start":122834453,"end":122862960,"strand":1,"description":"huntingtin interacting protein 1 related [Source:HGNC Symbol;Acc:HGNC:18415]"}, {"versioned_ensembl_gene_id":"ENSG00000225419.1","gene_symbol":"RPL21P3","gene_name":"ribosomal protein L21 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16533]","synonyms":"bA189K21.4","biotype":"processed_pseudogene","ncbi_id":"128760","summary":null,"start":18485265,"end":18486052,"strand":1,"description":"ribosomal protein L21 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16533]"}, {"versioned_ensembl_gene_id":"ENSG00000155760.2","gene_symbol":"FZD7","gene_name":"frizzled class receptor 7 [Source:HGNC Symbol;Acc:HGNC:4045]","synonyms":"FzE3","biotype":"protein_coding","ncbi_id":"8324","summary":" Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD7 protein contains an N-terminal signal sequence, 10 cysteine residues typical of the cysteine-rich extracellular domain of Fz family members, 7 putative transmembrane domains, and an intracellular C-terminal tail with a PDZ domain-binding motif. FZD7 gene expression may downregulate APC function and enhance beta-catenin-mediated signals in poorly differentiated human esophageal carcinomas. [provided by RefSeq, Jul 2008]","start":202034587,"end":202038445,"strand":1,"description":"frizzled class receptor 7 [Source:HGNC Symbol;Acc:HGNC:4045]"}, {"versioned_ensembl_gene_id":"ENSG00000167566.16","gene_symbol":"NCKAP5L","gene_name":"NCK associated protein 5 like [Source:HGNC Symbol;Acc:HGNC:29321]","synonyms":"KIAA1602","biotype":"protein_coding","ncbi_id":"57701","summary":null,"start":49791146,"end":49828750,"strand":-1,"description":"NCK associated protein 5 like [Source:HGNC Symbol;Acc:HGNC:29321]"}, {"versioned_ensembl_gene_id":"ENSG00000268510.1","gene_symbol":"IFNL3P1","gene_name":"interferon lambda 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44483]","synonyms":"IL28BP1","biotype":"unprocessed_pseudogene","ncbi_id":"100421129","summary":null,"start":39236433,"end":39237293,"strand":-1,"description":"interferon lambda 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44483]"}, {"versioned_ensembl_gene_id":"ENSG00000236926.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29707877,"end":29708299,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000197110.8","gene_symbol":"IFNL3","gene_name":"interferon lambda 3 [Source:HGNC Symbol;Acc:HGNC:18365]","synonyms":"IL28C,IL28B,IL-28B","biotype":"protein_coding","ncbi_id":"282617","summary":"This gene encodes a cytokine distantly related to type I interferons and the IL-10 family. This gene, interleukin 28A (IL28A), and interleukin 29 (IL29) are three closely related cytokine genes that form a cytokine gene cluster on a chromosomal region mapped to 19q13. Expression of the cytokines encoded by the three genes can be induced by viral infection. All three cytokines have been shown to interact with a heterodimeric class II cytokine receptor that consists of interleukin 10 receptor, beta (IL10RB) and interleukin 28 receptor, alpha (IL28RA). [provided by RefSeq, Jul 2008]","start":39243553,"end":39245129,"strand":-1,"description":"interferon lambda 3 [Source:HGNC Symbol;Acc:HGNC:18365]"}, {"versioned_ensembl_gene_id":"ENSG00000177954.11","gene_symbol":"RPS27","gene_name":"ribosomal protein S27 [Source:HGNC Symbol;Acc:HGNC:10416]","synonyms":"S27,MPS1,MPS-1","biotype":"protein_coding","ncbi_id":"6232","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the S27e family of ribosomal proteins and component of the 40S subunit. The encoded protein contains a C4-type zinc finger domain that can bind to zinc and may bind to nucleic acid. Mutations in this gene have been identified in numerous melanoma patients and in at least one patient with Diamond-Blackfan anemia (DBA). Elevated expression of this gene has been observed in various human cancers. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2018]","start":153990759,"end":153992150,"strand":1,"description":"ribosomal protein S27 [Source:HGNC Symbol;Acc:HGNC:10416]"}, {"versioned_ensembl_gene_id":"ENSG00000273345.5","gene_symbol":"AC104109.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":134205614,"end":134371044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249244.1","gene_symbol":"AC110373.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":119391831,"end":119395335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270177.1","gene_symbol":"AC104109.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134226410,"end":134227827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239615.1","gene_symbol":"AC104109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134267421,"end":134267856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198046.11","gene_symbol":"ZNF667","gene_name":"zinc finger protein 667 [Source:HGNC Symbol;Acc:HGNC:28854]","synonyms":"FLJ14011","biotype":"protein_coding","ncbi_id":"63934","summary":null,"start":56439325,"end":56478065,"strand":-1,"description":"zinc finger protein 667 [Source:HGNC Symbol;Acc:HGNC:28854]"}, {"versioned_ensembl_gene_id":"ENSG00000177535.8","gene_symbol":"OR2B11","gene_name":"olfactory receptor family 2 subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:31249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127623","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247449118,"end":247458105,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:31249]"}, {"versioned_ensembl_gene_id":"ENSG00000283050.1","gene_symbol":"GTF2IP12","gene_name":"general transcription factor IIi pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51723]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101926918","summary":null,"start":119407967,"end":119454638,"strand":-1,"description":"general transcription factor IIi pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51723]"}, {"versioned_ensembl_gene_id":"ENSG00000260780.1","gene_symbol":"AC087463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24206784,"end":24225854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260959.1","gene_symbol":"AC087463.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24238145,"end":24240192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272395.7","gene_symbol":"IFNL4","gene_name":"interferon lambda 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:44480]","synonyms":"IFNAN","biotype":"polymorphic_pseudogene","ncbi_id":"101180976","summary":"This gene is a polymorphic pseudogene which, in some humans, encodes the interferon (IFN) lambda 4 protein. Humans are polymorphic for the dinucleotide TT/deltaG allele. Compared to the ancestral state in non-human primates, the TT allele produces a frameshift in the coding region of this gene which is predicted to induce nonsense-mediated mRNA decay. This allele, and an allele in the first intron of this gene, have experienced a rapid increase in frequency and show indications of positive selection. The ancestral states of these alleles are associated with an impaired ability to clear hepatitis C virus. This gene, like other type III interferons (IFNs), interacts with the IFN lambda receptor complex (IFNLR) whose signaling is generally restricted to epithelial cells. This gene resides in a cluster of four type III IFN genes and at least two pseudogenes on chromosome 19q13.2. In general, interferons are produced in response to viral infection and block viral replication and propagation to uninfected cells by activating the JAK-STAT pathway and up-regulating antiviral genes. Multiple alternatively spliced transcripts have been described for this gene but their biological validity and protein coding status is still being ascertained. [provided by RefSeq, May 2017]","start":39246314,"end":39248856,"strand":-1,"description":"interferon lambda 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:44480]"}, {"versioned_ensembl_gene_id":"ENSG00000261621.1","gene_symbol":"AC087463.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24235078,"end":24276829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261598.1","gene_symbol":"AC087463.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24299749,"end":24300638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197301.7","gene_symbol":"AC090673.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65851340,"end":65882167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260760.1","gene_symbol":"PWRN3","gene_name":"Prader-Willi region non-protein coding RNA 3 [Source:HGNC Symbol;Acc:HGNC:49131]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928840","summary":null,"start":24441127,"end":24447967,"strand":1,"description":"Prader-Willi region non-protein coding RNA 3 [Source:HGNC Symbol;Acc:HGNC:49131]"}, {"versioned_ensembl_gene_id":"ENSG00000182329.12","gene_symbol":"KIAA2012","gene_name":"KIAA2012 [Source:HGNC Symbol;Acc:HGNC:51250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100652824","summary":null,"start":202073289,"end":202205203,"strand":1,"description":"KIAA2012 [Source:HGNC Symbol;Acc:HGNC:51250]"}, {"versioned_ensembl_gene_id":"ENSG00000136297.14","gene_symbol":"MMD2","gene_name":"monocyte to macrophage differentiation associated 2 [Source:HGNC Symbol;Acc:HGNC:30133]","synonyms":"PAQR10","biotype":"protein_coding","ncbi_id":"221938","summary":"This gene encodes a member of the PAQR (progestin and adipoQ receptor) family. Members of this family are evolutionarily conserved with significant sequence identity to bacterial hemolysin-like proteins and are defined by a set of seven transmembrane domains. The protein encoded by this gene localizes to the Golgi apparatus to modulate Ras signaling. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]","start":4905989,"end":4959213,"strand":-1,"description":"monocyte to macrophage differentiation associated 2 [Source:HGNC Symbol;Acc:HGNC:30133]"}, {"versioned_ensembl_gene_id":"ENSG00000196152.10","gene_symbol":"ZNF79","gene_name":"zinc finger protein 79 [Source:HGNC Symbol;Acc:HGNC:13153]","synonyms":"pT7","biotype":"protein_coding","ncbi_id":"7633","summary":null,"start":127424374,"end":127445372,"strand":1,"description":"zinc finger protein 79 [Source:HGNC Symbol;Acc:HGNC:13153]"}, {"versioned_ensembl_gene_id":"ENSG00000279996.1","gene_symbol":"AC004491.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75625089,"end":75626970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124160.11","gene_symbol":"NCOA5","gene_name":"nuclear receptor coactivator 5 [Source:HGNC Symbol;Acc:HGNC:15909]","synonyms":"CIA,bA465L10.6","biotype":"protein_coding","ncbi_id":"57727","summary":"This gene encodes a coregulator for the alpha and beta estrogen receptors and the orphan nuclear receptor NR1D2. The protein localizes to the nucleus, and is thought to have both coactivator and corepressor functions. Its interaction with nuclear receptors is independent of the AF2 domain on the receptors, which is known to regulate interaction with other coreceptors. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2017]","start":46060985,"end":46089952,"strand":-1,"description":"nuclear receptor coactivator 5 [Source:HGNC Symbol;Acc:HGNC:15909]"}, {"versioned_ensembl_gene_id":"ENSG00000248557.1","gene_symbol":"AC024558.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126624792,"end":126626061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282485.1","gene_symbol":"Z98882.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":528677,"end":530929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278711.1","gene_symbol":"AC007368.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126365344,"end":126367107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197763.14","gene_symbol":"TXNRD3","gene_name":"thioredoxin reductase 3 [Source:HGNC Symbol;Acc:HGNC:20667]","synonyms":"TRXR3,TR2,TGR","biotype":"protein_coding","ncbi_id":"114112","summary":"The protein encoded by this gene belongs to the pyridine nucleotide-disulfide oxidoreductase family, and is a member of the thioredoxin (Trx) system. Three thioredoxin reductase (TrxR) isozymes are found in mammals. TrxRs are selenocysteine-containing flavoenzymes, which reduce thioredoxins, as well as other substrates, and play a key role in redox homoeostasis. This gene encodes the third TrxR, which unlike the other two isozymes, contains an additional N-terminal glutaredoxin (Grx) domain, and shows highest expression in testis. The Grx domain allows this isozyme to participate in both Trx and glutathione systems. It functions as a homodimer containing FAD, and selenocysteine (Sec) at the active site. Sec is encoded by UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. Experimental evidence suggests the use of a non-AUG (CUG) codon as a translation initiation codon (PMID:20018845). [provided by RefSeq, Aug 2017]","start":126607052,"end":126655155,"strand":-1,"description":"thioredoxin reductase 3 [Source:HGNC Symbol;Acc:HGNC:20667]"}, {"versioned_ensembl_gene_id":"ENSG00000282214.1","gene_symbol":"CAPN15","gene_name":"calpain 15 [Source:HGNC Symbol;Acc:HGNC:11182]","synonyms":"SOLH","biotype":"processed_transcript","ncbi_id":"6650","summary":"This gene encodes a protein containing zinc-finger-like repeats and a calpain-like protease domain. The encoded protein may function as a transcription factor, RNA-binding protein, or in protein-protein interactions during visual system development. [provided by RefSeq, Jul 2008]","start":531239,"end":531551,"strand":1,"description":"calpain 15 [Source:HGNC Symbol;Acc:HGNC:11182]"}, {"versioned_ensembl_gene_id":"ENSG00000223107.1","gene_symbol":"RNU2-72P","gene_name":"RNA, U2 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:48565]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480702","summary":null,"start":60912765,"end":60912927,"strand":-1,"description":"RNA, U2 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:48565]"}, {"versioned_ensembl_gene_id":"ENSG00000136143.14","gene_symbol":"SUCLA2","gene_name":"succinate-CoA ligase ADP-forming beta subunit [Source:HGNC Symbol;Acc:HGNC:11448]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8803","summary":"Succinyl-CoA synthetase (SCS) is a mitochondrial matrix enzyme that acts as a heterodimer, being composed of an invariant alpha subunit and a substrate-specific beta subunit. The protein encoded by this gene is an ATP-specific SCS beta subunit that dimerizes with the SCS alpha subunit to form SCS-A, an essential component of the tricarboxylic acid cycle. SCS-A hydrolyzes ATP to convert succinate to succinyl-CoA. Defects in this gene are a cause of myopathic mitochondrial DNA depletion syndrome. A pseudogene of this gene has been found on chromosome 6. [provided by RefSeq, Jul 2008]","start":47936491,"end":48001354,"strand":-1,"description":"succinate-CoA ligase ADP-forming beta subunit [Source:HGNC Symbol;Acc:HGNC:11448]"}, {"versioned_ensembl_gene_id":"ENSG00000276226.1","gene_symbol":"AC007368.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126406834,"end":126411516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141480.17","gene_symbol":"ARRB2","gene_name":"arrestin beta 2 [Source:HGNC Symbol;Acc:HGNC:712]","synonyms":"DKFZp686L0365,BARR2,ARR2","biotype":"protein_coding","ncbi_id":"409","summary":"Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. Arrestin beta 2, like arrestin beta 1, was shown to inhibit beta-adrenergic receptor function in vitro. It is expressed at high levels in the central nervous system and may play a role in the regulation of synaptic receptors. Besides the brain, a cDNA for arrestin beta 2 was isolated from thyroid gland, and thus it may also be involved in hormone-specific desensitization of TSH receptors. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":4710489,"end":4721499,"strand":1,"description":"arrestin beta 2 [Source:HGNC Symbol;Acc:HGNC:712]"}, {"versioned_ensembl_gene_id":"ENSG00000149948.13","gene_symbol":"HMGA2","gene_name":"high mobility group AT-hook 2 [Source:HGNC Symbol;Acc:HGNC:5009]","synonyms":"LIPO,HMGIC,BABL","biotype":"protein_coding","ncbi_id":"8091","summary":"This gene encodes a protein that belongs to the non-histone chromosomal high mobility group (HMG) protein family. HMG proteins function as architectural factors and are essential components of the enhancesome. This protein contains structural DNA-binding domains and may act as a transcriptional regulating factor. Identification of the deletion, amplification, and rearrangement of this gene that are associated with myxoid liposarcoma suggests a role in adipogenesis and mesenchymal differentiation. A gene knock out study of the mouse counterpart demonstrated that this gene is involved in diet-induced obesity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":65824131,"end":65966295,"strand":1,"description":"high mobility group AT-hook 2 [Source:HGNC Symbol;Acc:HGNC:5009]"}, {"versioned_ensembl_gene_id":"ENSG00000197223.11","gene_symbol":"C1D","gene_name":"C1D nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:29911]","synonyms":"Rrp47,LRP1,SUNCOR,SUN-CoR","biotype":"protein_coding","ncbi_id":"10438","summary":"The protein encoded by this gene is a DNA binding and apoptosis-inducing protein and is localized in the nucleus. It is also a Rac3-interacting protein which acts as a corepressor for the thyroid hormone receptor. This protein is thought to regulate TRAX/Translin complex formation. Alternate splicing results in multiple transcript variants that encode the same protein. Multiple pseudogenes of this gene are found on chromosome 10.[provided by RefSeq, Jun 2010]","start":68041130,"end":68110948,"strand":-1,"description":"C1D nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:29911]"}, {"versioned_ensembl_gene_id":"ENSG00000243503.2","gene_symbol":"AC090453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36987977,"end":36988412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254038.1","gene_symbol":"AC092818.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37067441,"end":37069418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253650.1","gene_symbol":"SMARCE1P4","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39735]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642879","summary":null,"start":37095150,"end":37095390,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39735]"}, {"versioned_ensembl_gene_id":"ENSG00000047634.14","gene_symbol":"SCML1","gene_name":"sex comb on midleg like 1 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10580]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6322","summary":null,"start":17737449,"end":17754988,"strand":1,"description":"sex comb on midleg like 1 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:10580]"}, {"versioned_ensembl_gene_id":"ENSG00000253123.3","gene_symbol":"AC091182.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":37326575,"end":37331984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222035.3","gene_symbol":"AC079354.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":202113626,"end":202117058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253746.1","gene_symbol":"AC091182.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37405439,"end":37406724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227890.1","gene_symbol":"PSMA2P3","gene_name":"proteasome subunit alpha 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43834]","synonyms":"PSMA2L","biotype":"processed_pseudogene","ncbi_id":"79055","summary":null,"start":202179297,"end":202179971,"strand":1,"description":"proteasome subunit alpha 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43834]"}, {"versioned_ensembl_gene_id":"ENSG00000203664.7","gene_symbol":"OR2W5","gene_name":"olfactory receptor family 2 subfamily W member 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15424]","synonyms":"OST722,OR2W5P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene has a coding sequence that is comparable in length to other olfactory receptor genes, but it should be noted that a frameshift is present in the 3' coding region that disrupts the 7-transmembrane domain structure in the protein. It is unclear if the protein can function as an olfactory receptor or if an alternate function is served. For this reason, this gene has also been interpreted to be a pseudogene. [provided by RefSeq, Jan 2010]","start":247488093,"end":247492415,"strand":1,"description":"olfactory receptor family 2 subfamily W member 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15424]"}, {"versioned_ensembl_gene_id":"ENSG00000145284.11","gene_symbol":"SCD5","gene_name":"stearoyl-CoA desaturase 5 [Source:HGNC Symbol;Acc:HGNC:21088]","synonyms":"ACOD4,SCD4,HSCD5,FLJ21032,FADS4","biotype":"protein_coding","ncbi_id":"79966","summary":"Stearoyl-CoA desaturase (SCD; EC 1.14.99.5) is an integral membrane protein of the endoplasmic reticulum that catalyzes the formation of monounsaturated fatty acids from saturated fatty acids. SCD may be a key regulator of energy metabolism with a role in obesity and dislipidemia. Four SCD isoforms, Scd1 through Scd4, have been identified in mouse. In contrast, only 2 SCD isoforms, SCD1 (MIM 604031) and SCD5, have been identified in human. SCD1 shares about 85% amino acid identity with all 4 mouse SCD isoforms, as well as with rat Scd1 and Scd2. In contrast, SCD5 shares limited homology with the rodent SCDs and appears to be unique to primates (Wang et al., 2005 [PubMed 15907797]).[supplied by OMIM, Mar 2008]","start":82629539,"end":82798857,"strand":-1,"description":"stearoyl-CoA desaturase 5 [Source:HGNC Symbol;Acc:HGNC:21088]"}, {"versioned_ensembl_gene_id":"ENSG00000223825.5","gene_symbol":"DAZAP2P1","gene_name":"DAZ associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43869]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645805","summary":null,"start":202201384,"end":202201886,"strand":-1,"description":"DAZ associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43869]"}, {"versioned_ensembl_gene_id":"ENSG00000231903.1","gene_symbol":"AC079354.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":202178660,"end":202179391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243339.3","gene_symbol":"RN7SL738P","gene_name":"RNA, 7SL, cytoplasmic 738, pseudogene [Source:HGNC Symbol;Acc:HGNC:46754]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480695","summary":null,"start":196399911,"end":196400207,"strand":1,"description":"RNA, 7SL, cytoplasmic 738, pseudogene [Source:HGNC Symbol;Acc:HGNC:46754]"}, {"versioned_ensembl_gene_id":"ENSG00000228284.8","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32663658,"end":32684403,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000189376.11","gene_symbol":"C8orf76","gene_name":"chromosome 8 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25924]","synonyms":"FLJ14825","biotype":"protein_coding","ncbi_id":"84933","summary":null,"start":123219957,"end":123241398,"strand":-1,"description":"chromosome 8 open reading frame 76 [Source:HGNC Symbol;Acc:HGNC:25924]"}, {"versioned_ensembl_gene_id":"ENSG00000168509.19","gene_symbol":"HFE2","gene_name":"hemochromatosis type 2 (juvenile) [Source:HGNC Symbol;Acc:HGNC:4887]","synonyms":"RGMC,JH,HJV,HFE2A,hemojuvelin,haemojuvelin","biotype":"protein_coding","ncbi_id":"148738","summary":"The product of this gene is involved in iron metabolism. It may be a component of the signaling pathway which activates hepcidin or it may act as a modulator of hepcidin expression. It could also represent the cellular receptor for hepcidin. Two uORFs in the 5' UTR negatively regulate the expression and activity of the encoded protein. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. Defects in this gene are the cause of hemochromatosis type 2A, also called juvenile hemochromatosis (JH). JH is an early-onset autosomal recessive disorder due to severe iron overload resulting in hypogonadotrophic hypogonadism, hepatic fibrosis or cirrhosis and cardiomyopathy, occurring typically before age of 30. [provided by RefSeq, Oct 2015]","start":146017468,"end":146036746,"strand":-1,"description":"hemochromatosis type 2 (juvenile) [Source:HGNC Symbol;Acc:HGNC:4887]"}, {"versioned_ensembl_gene_id":"ENSG00000197958.12","gene_symbol":"RPL12","gene_name":"ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10302]","synonyms":"L12","biotype":"protein_coding","ncbi_id":"6136","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L11P family of ribosomal proteins. It is located in the cytoplasm. The protein binds directly to the 26S rRNA. This gene is co-transcribed with the U65 snoRNA, which is located in its fourth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":127447674,"end":127451405,"strand":-1,"description":"ribosomal protein L12 [Source:HGNC Symbol;Acc:HGNC:10302]"}, {"versioned_ensembl_gene_id":"ENSG00000163739.4","gene_symbol":"CXCL1","gene_name":"C-X-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:4602]","synonyms":"SCYB1,NAP-3,MGSA-a,MGSA,GROa,GRO1,FSP","biotype":"protein_coding","ncbi_id":"2919","summary":"This antimicrobial gene encodes a member of the CXC subfamily of chemokines. The encoded protein is a secreted growth factor that signals through the G-protein coupled receptor, CXC receptor 2. This protein plays a role in inflammation and as a chemoattractant for neutrophils. Aberrant expression of this protein is associated with the growth and progression of certain tumors. A naturally occurring processed form of this protein has increased chemotactic activity. Alternate splicing results in coding and non-coding variants of this gene. A pseudogene of this gene is found on chromosome 4. [provided by RefSeq, Sep 2014]","start":73869393,"end":73871242,"strand":1,"description":"C-X-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:4602]"}, {"versioned_ensembl_gene_id":"ENSG00000270480.1","gene_symbol":"AC073413.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82691737,"end":82692468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270842.1","gene_symbol":"AC073413.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82775461,"end":82776101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224231.1","gene_symbol":"LINC01832","gene_name":"long intergenic non-protein coding RNA 1832 [Source:HGNC Symbol;Acc:HGNC:52638]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373635","summary":null,"start":138101884,"end":138105905,"strand":1,"description":"long intergenic non-protein coding RNA 1832 [Source:HGNC Symbol;Acc:HGNC:52638]"}, {"versioned_ensembl_gene_id":"ENSG00000233045.1","gene_symbol":"AC097523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138278574,"end":138279210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000048828.16","gene_symbol":"FAM120A","gene_name":"family with sequence similarity 120A [Source:HGNC Symbol;Acc:HGNC:13247]","synonyms":"OSSA,KIAA0183,C9orf10","biotype":"protein_coding","ncbi_id":"23196","summary":null,"start":93451722,"end":93566107,"strand":1,"description":"family with sequence similarity 120A [Source:HGNC Symbol;Acc:HGNC:13247]"}, {"versioned_ensembl_gene_id":"ENSG00000166387.11","gene_symbol":"PPFIBP2","gene_name":"PPFIA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9250]","synonyms":"Cclp1","biotype":"protein_coding","ncbi_id":"8495","summary":"This gene encodes a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. The encoded protein is a beta liprin and plays a role in axon guidance and neuronal synapse development by recruiting LAR protein-tyrosine phosphatases to the plasma membrane. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":7513298,"end":7657127,"strand":1,"description":"PPFIA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9250]"}, {"versioned_ensembl_gene_id":"ENSG00000229074.8","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32723350,"end":32757450,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000125823.12","gene_symbol":"CSTL1","gene_name":"cystatin like 1 [Source:HGNC Symbol;Acc:HGNC:15958]","synonyms":"dJ322G13.4,CTES1","biotype":"protein_coding","ncbi_id":"128817","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located at the telomeric end of the cystatin locus and encodes a type 2 cystatin-like protein. The specific function of this protein has not been determined. [provided by RefSeq, Jul 2008]","start":23439685,"end":23444930,"strand":1,"description":"cystatin like 1 [Source:HGNC Symbol;Acc:HGNC:15958]"}, {"versioned_ensembl_gene_id":"ENSG00000096384.19","gene_symbol":"HSP90AB1","gene_name":"heat shock protein 90 alpha family class B member 1 [Source:HGNC Symbol;Acc:HGNC:5258]","synonyms":"HSPCB,HSPC2","biotype":"protein_coding","ncbi_id":"3326","summary":"This gene encodes a member of the heat shock protein 90 family; these proteins are involved in signal transduction, protein folding and degradation and morphological evolution. This gene encodes the constitutive form of the cytosolic 90 kDa heat-shock protein and is thought to play a role in gastric apoptosis and inflammation. Alternative splicing results in multiple transcript variants. Pseudogenes have been identified on multiple chromosomes. [provided by RefSeq, Dec 2012]","start":44246166,"end":44253888,"strand":1,"description":"heat shock protein 90 alpha family class B member 1 [Source:HGNC Symbol;Acc:HGNC:5258]"}, {"versioned_ensembl_gene_id":"ENSG00000276734.4","gene_symbol":"KIF5C","gene_name":"kinesin family member 5C [Source:HGNC Symbol;Acc:HGNC:6325]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3800","summary":"The protein encoded by this gene is a kinesin heavy chain subunit involved in the transport of cargo within the central nervous system. The encoded protein, which acts as a tetramer by associating with another heavy chain and two light chains, interacts with protein kinase CK2. Mutations in this gene have been associated with complex cortical dysplasia with other brain malformations-2. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Jul 2015]","start":148937284,"end":149030199,"strand":1,"description":"kinesin family member 5C [Source:HGNC Symbol;Acc:HGNC:6325]"}, {"versioned_ensembl_gene_id":"ENSG00000144233.9","gene_symbol":"AMMECR1L","gene_name":"AMMECR1 like [Source:HGNC Symbol;Acc:HGNC:28658]","synonyms":"MGC4268","biotype":"protein_coding","ncbi_id":"83607","summary":null,"start":127861630,"end":127885922,"strand":-1,"description":"AMMECR1 like [Source:HGNC Symbol;Acc:HGNC:28658]"}, {"versioned_ensembl_gene_id":"ENSG00000234645.3","gene_symbol":"YWHAEP5","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49439]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440917","summary":null,"start":138288029,"end":138288793,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49439]"}, {"versioned_ensembl_gene_id":"ENSG00000124151.18","gene_symbol":"NCOA3","gene_name":"nuclear receptor coactivator 3 [Source:HGNC Symbol;Acc:HGNC:7670]","synonyms":"TNRC16,SRC3,SRC-3,RAC3,p/CIP,KAT13B,CAGH16,bHLHe42,AIB1,ACTR,TRAM-1","biotype":"protein_coding","ncbi_id":"8202","summary":"The protein encoded by this gene is a nuclear receptor coactivator that interacts with nuclear hormone receptors to enhance their transcriptional activator functions. The encoded protein has histone acetyltransferase activity and recruits p300/CBP-associated factor and CREB binding protein as part of a multisubunit coactivation complex. This protein is initially found in the cytoplasm but is translocated into the nucleus upon phosphorylation. Several transcript variants encoding different isoforms have been found for this gene. In addition, a polymorphic repeat region is found in the C-terminus of the encoded protein. [provided by RefSeq, Mar 2010]","start":47501902,"end":47656877,"strand":1,"description":"nuclear receptor coactivator 3 [Source:HGNC Symbol;Acc:HGNC:7670]"}, {"versioned_ensembl_gene_id":"ENSG00000203644.3","gene_symbol":"AC083799.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":129847048,"end":129847957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000029363.16","gene_symbol":"BCLAF1","gene_name":"BCL2 associated transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:16863]","synonyms":"KIAA0164,BTF","biotype":"protein_coding","ncbi_id":"9774","summary":"This gene encodes a transcriptional repressor that interacts with several members of the BCL2 family of proteins. Overexpression of this protein induces apoptosis, which can be suppressed by co-expression of BCL2 proteins. The protein localizes to dot-like structures throughout the nucleus, and redistributes to a zone near the nuclear envelope in cells undergoing apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":136256627,"end":136289851,"strand":-1,"description":"BCL2 associated transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:16863]"}, {"versioned_ensembl_gene_id":"ENSG00000095932.6","gene_symbol":"SMIM24","gene_name":"small integral membrane protein 24 [Source:HGNC Symbol;Acc:HGNC:37244]","synonyms":"HSPC323,C19orf77","biotype":"protein_coding","ncbi_id":"284422","summary":null,"start":3473986,"end":3480542,"strand":-1,"description":"small integral membrane protein 24 [Source:HGNC Symbol;Acc:HGNC:37244]"}, {"versioned_ensembl_gene_id":"ENSG00000275517.4","gene_symbol":"PRB1","gene_name":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]","synonyms":"PRB1M,PRB1L,PMS,PMF,PM","biotype":"protein_coding","ncbi_id":"5542","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Medium\" allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015]","start":11351822,"end":11356402,"strand":-1,"description":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]"}, {"versioned_ensembl_gene_id":"ENSG00000172765.16","gene_symbol":"TMCC1","gene_name":"transmembrane and coiled-coil domain family 1 [Source:HGNC Symbol;Acc:HGNC:29116]","synonyms":"KIAA0779","biotype":"protein_coding","ncbi_id":"23023","summary":null,"start":129647792,"end":129893576,"strand":-1,"description":"transmembrane and coiled-coil domain family 1 [Source:HGNC Symbol;Acc:HGNC:29116]"}, {"versioned_ensembl_gene_id":"ENSG00000165156.14","gene_symbol":"ZHX1","gene_name":"zinc fingers and homeoboxes 1 [Source:HGNC Symbol;Acc:HGNC:12871]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11244","summary":"The members of the zinc fingers and homeoboxes gene family are nuclear homodimeric transcriptional repressors that interact with the A subunit of nuclear factor-Y (NF-YA) and contain two C2H2-type zinc fingers and five homeobox DNA-binding domains. This gene encodes member 1 of this gene family. In addition to forming homodimers, this protein heterodimerizes with members 2 and 3 of the zinc fingers and homeoboxes family. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 8 open reading frame 76 (C8orf76) gene. [provided by RefSeq, Feb 2011]","start":123248451,"end":123275541,"strand":-1,"description":"zinc fingers and homeoboxes 1 [Source:HGNC Symbol;Acc:HGNC:12871]"}, {"versioned_ensembl_gene_id":"ENSG00000231433.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31278540,"end":31279994,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000213820.3","gene_symbol":"RPL13P2","gene_name":"ribosomal protein L13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16342]","synonyms":"RPL13P3,dJ599F21.2","biotype":"processed_pseudogene","ncbi_id":"128500","summary":null,"start":46099518,"end":46100176,"strand":1,"description":"ribosomal protein L13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16342]"}, {"versioned_ensembl_gene_id":"ENSG00000200547.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":116452536,"end":116452627,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201612.1","gene_symbol":"RN7SKP15","gene_name":"RNA, 7SK small nuclear pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:45739]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480456","summary":null,"start":27806082,"end":27806390,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:45739]"}, {"versioned_ensembl_gene_id":"ENSG00000243446.3","gene_symbol":"RN7SL284P","gene_name":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480999","summary":null,"start":77912271,"end":77912545,"strand":-1,"description":"RNA, 7SL, cytoplasmic 284, pseudogene [Source:HGNC Symbol;Acc:HGNC:46300]"}, {"versioned_ensembl_gene_id":"ENSG00000200310.1","gene_symbol":"RNA5SP215","gene_name":"RNA, 5S ribosomal pseudogene 215 [Source:HGNC Symbol;Acc:HGNC:43115]","synonyms":"RN5S215","biotype":"rRNA","ncbi_id":"100873475","summary":null,"start":120686621,"end":120686742,"strand":1,"description":"RNA, 5S ribosomal pseudogene 215 [Source:HGNC Symbol;Acc:HGNC:43115]"}, {"versioned_ensembl_gene_id":"ENSG00000233841.11","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31259794,"end":31263175,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000249920.2","gene_symbol":"HNRNPA1P55","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:48785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642958","summary":null,"start":73938604,"end":73939558,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:48785]"}, {"versioned_ensembl_gene_id":"ENSG00000230886.3","gene_symbol":"HMGB1P25","gene_name":"high mobility group box 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644651","summary":null,"start":9018293,"end":9018899,"strand":-1,"description":"high mobility group box 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39116]"}, {"versioned_ensembl_gene_id":"ENSG00000271344.1","gene_symbol":"AC018638.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128690451,"end":128691717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272192.1","gene_symbol":"AC100812.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65842752,"end":65843331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250339.2","gene_symbol":"CXCL1P1","gene_name":"C-X-C motif chemokine ligand 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10641]","synonyms":"SCYB1P,MGSAP,GROP,GRO1P,CXCL1P","biotype":"processed_pseudogene","ncbi_id":"50612","summary":null,"start":73944011,"end":73944324,"strand":-1,"description":"C-X-C motif chemokine ligand 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10641]"}, {"versioned_ensembl_gene_id":"ENSG00000270289.1","gene_symbol":"AC012669.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180473137,"end":180473419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264582.2","gene_symbol":"RN7SL326P","gene_name":"RNA, 7SL, cytoplasmic 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:46342]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479342","summary":null,"start":40804846,"end":40805141,"strand":1,"description":"RNA, 7SL, cytoplasmic 326, pseudogene [Source:HGNC Symbol;Acc:HGNC:46342]"}, {"versioned_ensembl_gene_id":"ENSG00000206863.1","gene_symbol":"RNU5A-6P","gene_name":"RNA, U5A small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42527]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873871","summary":null,"start":24124170,"end":24124285,"strand":-1,"description":"RNA, U5A small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42527]"}, {"versioned_ensembl_gene_id":"ENSG00000252857.1","gene_symbol":"RNU6-389P","gene_name":"RNA, U6 small nuclear 389, pseudogene [Source:HGNC Symbol;Acc:HGNC:47352]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481301","summary":null,"start":55685977,"end":55686081,"strand":1,"description":"RNA, U6 small nuclear 389, pseudogene [Source:HGNC Symbol;Acc:HGNC:47352]"}, {"versioned_ensembl_gene_id":"ENSG00000278779.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":38532589,"end":38532707,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000201066.1","gene_symbol":"RN7SKP280","gene_name":"RNA, 7SK small nuclear pseudogene 280 [Source:HGNC Symbol;Acc:HGNC:46004]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479220","summary":null,"start":155181881,"end":155182184,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 280 [Source:HGNC Symbol;Acc:HGNC:46004]"}, {"versioned_ensembl_gene_id":"ENSG00000252619.1","gene_symbol":"RNU6-1149P","gene_name":"RNA, U6 small nuclear 1149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48112]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481542","summary":null,"start":42417497,"end":42417593,"strand":-1,"description":"RNA, U6 small nuclear 1149, pseudogene [Source:HGNC Symbol;Acc:HGNC:48112]"}, {"versioned_ensembl_gene_id":"ENSG00000223156.1","gene_symbol":"RNU2-18P","gene_name":"RNA, U2 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:48511]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480205","summary":null,"start":16476003,"end":16476164,"strand":1,"description":"RNA, U2 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:48511]"}, {"versioned_ensembl_gene_id":"ENSG00000212321.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":122840426,"end":122840645,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000212623.1","gene_symbol":"RNU6-493P","gene_name":"RNA, U6 small nuclear 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:47456]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481336","summary":null,"start":80900757,"end":80900864,"strand":1,"description":"RNA, U6 small nuclear 493, pseudogene [Source:HGNC Symbol;Acc:HGNC:47456]"}, {"versioned_ensembl_gene_id":"ENSG00000278334.1","gene_symbol":"HOXA11-AS1_2","gene_name":"HOXA11 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02138]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27185832,"end":27186018,"strand":1,"description":"HOXA11 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02138]"}, {"versioned_ensembl_gene_id":"ENSG00000207023.1","gene_symbol":"RNU6-975P","gene_name":"RNA, U6 small nuclear 975, pseudogene [Source:HGNC Symbol;Acc:HGNC:47938]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479997","summary":null,"start":73464073,"end":73464177,"strand":1,"description":"RNA, U6 small nuclear 975, pseudogene [Source:HGNC Symbol;Acc:HGNC:47938]"}, {"versioned_ensembl_gene_id":"ENSG00000199326.1","gene_symbol":"RNU6-1298P","gene_name":"RNA, U6 small nuclear 1298, pseudogene [Source:HGNC Symbol;Acc:HGNC:48261]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481590","summary":null,"start":88226729,"end":88226829,"strand":1,"description":"RNA, U6 small nuclear 1298, pseudogene [Source:HGNC Symbol;Acc:HGNC:48261]"}, {"versioned_ensembl_gene_id":"ENSG00000211991.4","gene_symbol":"MIR676","gene_name":"microRNA 676 [Source:HGNC Symbol;Acc:HGNC:38880]","synonyms":"hsa-mir-676","biotype":"miRNA","ncbi_id":"100500887","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70022857,"end":70022923,"strand":1,"description":"microRNA 676 [Source:HGNC Symbol;Acc:HGNC:38880]"}, {"versioned_ensembl_gene_id":"ENSG00000203286.5","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128745857,"end":128746138,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238554.1","gene_symbol":"RNU1-88P","gene_name":"RNA, U1 small nuclear 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:48430]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481619","summary":null,"start":36639545,"end":36639672,"strand":-1,"description":"RNA, U1 small nuclear 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:48430]"}, {"versioned_ensembl_gene_id":"ENSG00000263950.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30726562,"end":30726672,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200097.1","gene_symbol":"RNU6-1167P","gene_name":"RNA, U6 small nuclear 1167, pseudogene [Source:HGNC Symbol;Acc:HGNC:48130]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480407","summary":null,"start":35250959,"end":35251052,"strand":-1,"description":"RNA, U6 small nuclear 1167, pseudogene [Source:HGNC Symbol;Acc:HGNC:48130]"}, {"versioned_ensembl_gene_id":"ENSG00000199979.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68885576,"end":68885677,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263697.1","gene_symbol":"MIR3621","gene_name":"microRNA 3621 [Source:HGNC Symbol;Acc:HGNC:38930]","synonyms":"hsa-mir-3621","biotype":"miRNA","ncbi_id":"100500811","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":137169186,"end":137169270,"strand":-1,"description":"microRNA 3621 [Source:HGNC Symbol;Acc:HGNC:38930]"}, {"versioned_ensembl_gene_id":"ENSG00000207503.1","gene_symbol":"SNORA32","gene_name":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":41539206,"end":41539326,"strand":1,"description":"Small nucleolar RNA SNORA32 [Source:RFAM;Acc:RF00421]"}, {"versioned_ensembl_gene_id":"ENSG00000264792.1","gene_symbol":"MIR4637","gene_name":"microRNA 4637 [Source:HGNC Symbol;Acc:HGNC:41651]","synonyms":"hsa-mir-4637","biotype":"miRNA","ncbi_id":"100616271","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14825929,"end":14826012,"strand":-1,"description":"microRNA 4637 [Source:HGNC Symbol;Acc:HGNC:41651]"}, {"versioned_ensembl_gene_id":"ENSG00000240189.3","gene_symbol":"RN7SL621P","gene_name":"RNA, 7SL, cytoplasmic 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:46637]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479449","summary":null,"start":33580210,"end":33580508,"strand":-1,"description":"RNA, 7SL, cytoplasmic 621, pseudogene [Source:HGNC Symbol;Acc:HGNC:46637]"}, {"versioned_ensembl_gene_id":"ENSG00000199566.1","gene_symbol":"SNORA64","gene_name":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]","synonyms":"U64,RNU64","biotype":"snoRNA","ncbi_id":"26784","summary":null,"start":47346166,"end":47346297,"strand":-1,"description":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]"}, {"versioned_ensembl_gene_id":"ENSG00000200151.1","gene_symbol":"RN7SKP231","gene_name":"RNA, 7SK small nuclear pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:45955]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479198","summary":null,"start":91594965,"end":91595241,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 231 [Source:HGNC Symbol;Acc:HGNC:45955]"}, {"versioned_ensembl_gene_id":"ENSG00000278161.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,FB1,FB1,INO80F,INO80F,amida","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000206708.1","gene_symbol":"RNU6-1227P","gene_name":"RNA, U6 small nuclear 1227, pseudogene [Source:HGNC Symbol;Acc:HGNC:48190]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481567","summary":null,"start":39025987,"end":39026093,"strand":1,"description":"RNA, U6 small nuclear 1227, pseudogene [Source:HGNC Symbol;Acc:HGNC:48190]"}, {"versioned_ensembl_gene_id":"ENSG00000263701.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31413150,"end":31413256,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000216195.3","gene_symbol":"MIR941-4","gene_name":"microRNA 941-4 [Source:HGNC Symbol;Acc:HGNC:33687]","synonyms":"MIRN941-4,hsa-mir-941-4","biotype":"miRNA","ncbi_id":"100126330","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919756,"end":63919827,"strand":1,"description":"microRNA 941-4 [Source:HGNC Symbol;Acc:HGNC:33687]"}, {"versioned_ensembl_gene_id":"ENSG00000212392.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":57493667,"end":57493780,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275606.1","gene_symbol":"CR388407.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29064006,"end":29076532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277387.1","gene_symbol":"MIR8058","gene_name":"microRNA 8058 [Source:HGNC Symbol;Acc:HGNC:50018]","synonyms":"hsa-mir-8058","biotype":"miRNA","ncbi_id":"102465863","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82688931,"end":82689019,"strand":1,"description":"microRNA 8058 [Source:HGNC Symbol;Acc:HGNC:50018]"}, {"versioned_ensembl_gene_id":"ENSG00000276152.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30951585,"end":30951821,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000273717.1","gene_symbol":"RN7SL343P","gene_name":"RNA, 7SL, cytoplasmic 343, pseudogene [Source:HGNC Symbol;Acc:HGNC:46359]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481018","summary":null,"start":42011350,"end":42011610,"strand":1,"description":"RNA, 7SL, cytoplasmic 343, pseudogene [Source:HGNC Symbol;Acc:HGNC:46359]"}, {"versioned_ensembl_gene_id":"ENSG00000212510.1","gene_symbol":"RNU6-972P","gene_name":"RNA, U6 small nuclear 972, pseudogene [Source:HGNC Symbol;Acc:HGNC:47935]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479995","summary":null,"start":136773999,"end":136774105,"strand":1,"description":"RNA, U6 small nuclear 972, pseudogene [Source:HGNC Symbol;Acc:HGNC:47935]"}, {"versioned_ensembl_gene_id":"ENSG00000239043.1","gene_symbol":"SNORD127","gene_name":"small nucleolar RNA, C/D box 127 [Source:HGNC Symbol;Acc:HGNC:33555]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113389","summary":null,"start":45110883,"end":45110968,"strand":1,"description":"small nucleolar RNA, C/D box 127 [Source:HGNC Symbol;Acc:HGNC:33555]"}, {"versioned_ensembl_gene_id":"ENSG00000200215.3","gene_symbol":"SNORD113-6","gene_name":"small nucleolar RNA, C/D box 113-6 [Source:HGNC Symbol;Acc:HGNC:32985]","synonyms":"14q(I-6)","biotype":"snoRNA","ncbi_id":"767566","summary":null,"start":100939556,"end":100939630,"strand":1,"description":"small nucleolar RNA, C/D box 113-6 [Source:HGNC Symbol;Acc:HGNC:32985]"}, {"versioned_ensembl_gene_id":"ENSG00000202379.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"U70,DXS648E,RNU70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":108574565,"end":108574698,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000265810.1","gene_symbol":"MIR3907","gene_name":"microRNA 3907 [Source:HGNC Symbol;Acc:HGNC:38988]","synonyms":"hsa-mir-3907","biotype":"miRNA","ncbi_id":"100500835","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151433489,"end":151433639,"strand":-1,"description":"microRNA 3907 [Source:HGNC Symbol;Acc:HGNC:38988]"}, {"versioned_ensembl_gene_id":"ENSG00000264474.1","gene_symbol":"MIR4656","gene_name":"microRNA 4656 [Source:HGNC Symbol;Acc:HGNC:41749]","synonyms":"hsa-mir-4656","biotype":"miRNA","ncbi_id":"100616465","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4788565,"end":4788639,"strand":-1,"description":"microRNA 4656 [Source:HGNC Symbol;Acc:HGNC:41749]"}, {"versioned_ensembl_gene_id":"ENSG00000273937.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":149259,"end":149348,"strand":1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000239923.3","gene_symbol":"RN7SL864P","gene_name":"RNA, 7SL, cytoplasmic 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:46880]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479536","summary":null,"start":14223041,"end":14223325,"strand":1,"description":"RNA, 7SL, cytoplasmic 864, pseudogene [Source:HGNC Symbol;Acc:HGNC:46880]"}, {"versioned_ensembl_gene_id":"ENSG00000273833.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"amida,FB1,FB1,INO80F,INO80F,amida","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000263515.1","gene_symbol":"MIR548AN","gene_name":"microRNA 548an [Source:HGNC Symbol;Acc:HGNC:41681]","synonyms":"hsa-mir-548an","biotype":"miRNA","ncbi_id":"100616144","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":106639814,"end":106639896,"strand":1,"description":"microRNA 548an [Source:HGNC Symbol;Acc:HGNC:41681]"}, {"versioned_ensembl_gene_id":"ENSG00000284378.1","gene_symbol":"MIR1244-1","gene_name":"microRNA 1244-1 [Source:HGNC Symbol;Acc:HGNC:35310]","synonyms":"MIRN1244,MIR1244,hsa-mir-1244","biotype":"miRNA","ncbi_id":"100302285","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":231713314,"end":231713398,"strand":1,"description":"microRNA 1244-1 [Source:HGNC Symbol;Acc:HGNC:35310]"}, {"versioned_ensembl_gene_id":"ENSG00000284433.1","gene_symbol":"MIR1914","gene_name":"microRNA 1914 [Source:HGNC Symbol;Acc:HGNC:35398]","synonyms":"MIRN1914,hsa-mir-1914","biotype":"miRNA","ncbi_id":"100302137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63941465,"end":63941544,"strand":-1,"description":"microRNA 1914 [Source:HGNC Symbol;Acc:HGNC:35398]"}, {"versioned_ensembl_gene_id":"ENSG00000201699.1","gene_symbol":"RNU1-59P","gene_name":"RNA, U1 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:48401]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480167","summary":null,"start":149162783,"end":149162944,"strand":-1,"description":"RNA, U1 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:48401]"}, {"versioned_ensembl_gene_id":"ENSG00000199270.1","gene_symbol":"RNA5S12","gene_name":"RNA, 5S ribosomal 12 [Source:HGNC Symbol;Acc:HGNC:34373]","synonyms":"RN5S12","biotype":"rRNA","ncbi_id":"100169763","summary":null,"start":228634871,"end":228634989,"strand":-1,"description":"RNA, 5S ribosomal 12 [Source:HGNC Symbol;Acc:HGNC:34373]"}, {"versioned_ensembl_gene_id":"ENSG00000212226.1","gene_symbol":"RNU6-907P","gene_name":"RNA, U6 small nuclear 907, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000210839.1","gene_symbol":"RNU6ATAC5P","gene_name":"RNA, U6atac small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:34095]","synonyms":null,"biotype":"snRNA","ncbi_id":"100151688","summary":null,"start":73026748,"end":73026873,"strand":1,"description":"RNA, U6atac small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:34095]"}, {"versioned_ensembl_gene_id":"ENSG00000222579.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":104851824,"end":104851918,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000262922.1","gene_symbol":"RNU6-164P","gene_name":"RNA, U6 small nuclear 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:47127]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479639","summary":null,"start":162477891,"end":162477993,"strand":1,"description":"RNA, U6 small nuclear 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:47127]"}, {"versioned_ensembl_gene_id":"ENSG00000274098.1","gene_symbol":"RN7SL787P","gene_name":"RNA, 7SL, cytoplasmic 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:46803]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479507","summary":null,"start":67791499,"end":67791782,"strand":-1,"description":"RNA, 7SL, cytoplasmic 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:46803]"}, {"versioned_ensembl_gene_id":"ENSG00000264554.2","gene_symbol":"RN7SL793P","gene_name":"RNA, 7SL, cytoplasmic 793, pseudogene [Source:HGNC Symbol;Acc:HGNC:46809]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481137","summary":null,"start":102217318,"end":102217613,"strand":-1,"description":"RNA, 7SL, cytoplasmic 793, pseudogene [Source:HGNC Symbol;Acc:HGNC:46809]"}, {"versioned_ensembl_gene_id":"ENSG00000284334.1","gene_symbol":"MIR4651","gene_name":"microRNA 4651 [Source:HGNC Symbol;Acc:HGNC:41647]","synonyms":"hsa-mir-4651","biotype":"miRNA","ncbi_id":"100616270","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75915197,"end":75915269,"strand":1,"description":"microRNA 4651 [Source:HGNC Symbol;Acc:HGNC:41647]"}, {"versioned_ensembl_gene_id":"ENSG00000222931.1","gene_symbol":"RN7SKP205","gene_name":"RNA, 7SK small nuclear pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:45929]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479186","summary":null,"start":23791930,"end":23792236,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 205 [Source:HGNC Symbol;Acc:HGNC:45929]"}, {"versioned_ensembl_gene_id":"ENSG00000266745.1","gene_symbol":"MIR3135A","gene_name":"microRNA 3135a [Source:HGNC Symbol;Acc:HGNC:38199]","synonyms":"MIR3135,hsa-mir-3135","biotype":"miRNA","ncbi_id":"100422901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20137565,"end":20137641,"strand":1,"description":"microRNA 3135a [Source:HGNC Symbol;Acc:HGNC:38199]"}, {"versioned_ensembl_gene_id":"ENSG00000266808.1","gene_symbol":"MIR548AE1","gene_name":"microRNA 548ae-1 [Source:HGNC Symbol;Acc:HGNC:41742]","synonyms":"hsa-mir-548ae-1","biotype":"miRNA","ncbi_id":"100616305","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":184378975,"end":184379044,"strand":1,"description":"microRNA 548ae-1 [Source:HGNC Symbol;Acc:HGNC:41742]"}, {"versioned_ensembl_gene_id":"ENSG00000199222.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":21481716,"end":21481817,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265074.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32672452,"end":32672615,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000265694.1","gene_symbol":"MIR4774","gene_name":"microRNA 4774 [Source:HGNC Symbol;Acc:HGNC:41873]","synonyms":"hsa-mir-4774","biotype":"miRNA","ncbi_id":"100616356","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168582943,"end":168583018,"strand":1,"description":"microRNA 4774 [Source:HGNC Symbol;Acc:HGNC:41873]"}, {"versioned_ensembl_gene_id":"ENSG00000206979.1","gene_symbol":"SNORD61","gene_name":"small nucleolar RNA, C/D box 61 [Source:HGNC Symbol;Acc:HGNC:10218]","synonyms":"U61,RNU61,HBII-342","biotype":"snoRNA","ncbi_id":"26787","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in an intron of the RNA binding motif protein, X-linked gene (RBMX). [provided by RefSeq, Sep 2009]","start":136879199,"end":136879271,"strand":-1,"description":"small nucleolar RNA, C/D box 61 [Source:HGNC Symbol;Acc:HGNC:10218]"}, {"versioned_ensembl_gene_id":"ENSG00000212379.1","gene_symbol":"RNU6-269P","gene_name":"RNA, U6 small nuclear 269, pseudogene [Source:HGNC Symbol;Acc:HGNC:47232]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481263","summary":null,"start":58378052,"end":58378148,"strand":-1,"description":"RNA, U6 small nuclear 269, pseudogene [Source:HGNC Symbol;Acc:HGNC:47232]"}, {"versioned_ensembl_gene_id":"ENSG00000206834.1","gene_symbol":"SNORA1","gene_name":"small nucleolar RNA, H/ACA box 1 [Source:HGNC Symbol;Acc:HGNC:32557]","synonyms":"ACA1","biotype":"snoRNA","ncbi_id":"677792","summary":null,"start":93732004,"end":93732133,"strand":-1,"description":"small nucleolar RNA, H/ACA box 1 [Source:HGNC Symbol;Acc:HGNC:32557]"}, {"versioned_ensembl_gene_id":"ENSG00000221055.1","gene_symbol":"MIR1302-3","gene_name":"microRNA 1302-3 [Source:HGNC Symbol;Acc:HGNC:35295]","synonyms":"MIRN1302-3,hsa-mir-1302-3","biotype":"miRNA","ncbi_id":"100302128","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113582959,"end":113583096,"strand":-1,"description":"microRNA 1302-3 [Source:HGNC Symbol;Acc:HGNC:35295]"}, {"versioned_ensembl_gene_id":"ENSG00000275394.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30263132,"end":30263264,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000240837.3","gene_symbol":"RN7SL77P","gene_name":"RNA, 7SL, cytoplasmic 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:46093]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479252","summary":null,"start":70610086,"end":70610379,"strand":1,"description":"RNA, 7SL, cytoplasmic 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:46093]"}, {"versioned_ensembl_gene_id":"ENSG00000207277.1","gene_symbol":"RNA5SP284","gene_name":"RNA, 5S ribosomal pseudogene 284 [Source:HGNC Symbol;Acc:HGNC:43184]","synonyms":"RN5S284","biotype":"rRNA","ncbi_id":"100873537","summary":null,"start":63813190,"end":63813307,"strand":1,"description":"RNA, 5S ribosomal pseudogene 284 [Source:HGNC Symbol;Acc:HGNC:43184]"}, {"versioned_ensembl_gene_id":"ENSG00000273573.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":181668749,"end":181669028,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000277569.1","gene_symbol":"MIR6134","gene_name":"microRNA 6134 [Source:HGNC Symbol;Acc:HGNC:49951]","synonyms":"hsa-mir-6134","biotype":"miRNA","ncbi_id":"102465140","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28495555,"end":28495663,"strand":-1,"description":"microRNA 6134 [Source:HGNC Symbol;Acc:HGNC:49951]"}, {"versioned_ensembl_gene_id":"ENSG00000208015.1","gene_symbol":"MIR362","gene_name":"microRNA 362 [Source:HGNC Symbol;Acc:HGNC:32022]","synonyms":"MIRN362,hsa-mir-362","biotype":"miRNA","ncbi_id":"574030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50008964,"end":50009028,"strand":1,"description":"microRNA 362 [Source:HGNC Symbol;Acc:HGNC:32022]"}, {"versioned_ensembl_gene_id":"ENSG00000263979.1","gene_symbol":"MIR4672","gene_name":"microRNA 4672 [Source:HGNC Symbol;Acc:HGNC:41662]","synonyms":"hsa-mir-4672","biotype":"miRNA","ncbi_id":"100616429","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127869415,"end":127869495,"strand":-1,"description":"microRNA 4672 [Source:HGNC Symbol;Acc:HGNC:41662]"}, {"versioned_ensembl_gene_id":"ENSG00000202048.1","gene_symbol":"SNORD114-20","gene_name":"small nucleolar RNA, C/D box 114-20 [Source:HGNC Symbol;Acc:HGNC:33008]","synonyms":"14q(II-20)","biotype":"snoRNA","ncbi_id":"767598","summary":null,"start":100981004,"end":100981075,"strand":1,"description":"small nucleolar RNA, C/D box 114-20 [Source:HGNC Symbol;Acc:HGNC:33008]"}, {"versioned_ensembl_gene_id":"ENSG00000222499.1","gene_symbol":"RN7SKP177","gene_name":"RNA, 7SK small nuclear pseudogene 177 [Source:HGNC Symbol;Acc:HGNC:45901]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479174","summary":null,"start":157017342,"end":157017696,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 177 [Source:HGNC Symbol;Acc:HGNC:45901]"}, {"versioned_ensembl_gene_id":"ENSG00000239168.1","gene_symbol":"RNU7-197P","gene_name":"RNA, U7 small nuclear 197 pseudogene [Source:HGNC Symbol;Acc:HGNC:45731]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480455","summary":null,"start":148991572,"end":148991633,"strand":-1,"description":"RNA, U7 small nuclear 197 pseudogene [Source:HGNC Symbol;Acc:HGNC:45731]"}, {"versioned_ensembl_gene_id":"ENSG00000207208.1","gene_symbol":"RNU6-790P","gene_name":"RNA, U6 small nuclear 790, pseudogene [Source:HGNC Symbol;Acc:HGNC:47753]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481430","summary":null,"start":101803227,"end":101803331,"strand":1,"description":"RNA, U6 small nuclear 790, pseudogene [Source:HGNC Symbol;Acc:HGNC:47753]"}, {"versioned_ensembl_gene_id":"ENSG00000274585.1","gene_symbol":"RNU2-1","gene_name":"RNA, U2 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10142]","synonyms":"U2","biotype":"snRNA","ncbi_id":"6066","summary":"The spliceosome is a multicomponent ribonucleoprotein complex that catalyzes the removal of introns from nuclear mRNA precursors. The spliceosome is composed of four small ribonucleoprotein particles (the U1, U2, and U4/U6 snRNPs) and numerous additional proteins. The U2 small nuclear RNA (snRNA) is a RNA component of the U2 snRNP that interacts with the 3' region of the intron at the branch site. Several sites in the human genome express U2 snRNAs. This locus represents an array of U2 snRNA genes located at 17q21-22 that undergoes concerted evolution to homogenize repeat units within the array. Each repeat in this array is approximately 6.1 kb long and contains a single copy of the U2 snRNA. Arrays of six to more than 30 repeats have been reported. [provided by RefSeq, Mar 2009]","start":43233787,"end":43233977,"strand":-1,"description":"RNA, U2 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10142]"}, {"versioned_ensembl_gene_id":"ENSG00000207417.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":74376687,"end":74376793,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264185.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31360589,"end":31360695,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207475.1","gene_symbol":"SNORA80E","gene_name":"small nucleolar RNA, H/ACA box 80E [Source:HGNC Symbol;Acc:HGNC:32635]","synonyms":"SNORA42,ACA42","biotype":"snoRNA","ncbi_id":"677823","summary":null,"start":155919909,"end":155920045,"strand":-1,"description":"small nucleolar RNA, H/ACA box 80E [Source:HGNC Symbol;Acc:HGNC:32635]"}, {"versioned_ensembl_gene_id":"ENSG00000252583.2","gene_symbol":"MIR514B","gene_name":"microRNA 514b [Source:HGNC Symbol;Acc:HGNC:38292]","synonyms":"hsa-mir-514b","biotype":"miRNA","ncbi_id":"100422847","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147250151,"end":147250230,"strand":-1,"description":"microRNA 514b [Source:HGNC Symbol;Acc:HGNC:38292]"}, {"versioned_ensembl_gene_id":"ENSG00000199153.1","gene_symbol":"MIR30D","gene_name":"microRNA 30d [Source:HGNC Symbol;Acc:HGNC:31628]","synonyms":"MIRN30D,hsa-mir-30d","biotype":"miRNA","ncbi_id":"407033","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134804876,"end":134804945,"strand":-1,"description":"microRNA 30d [Source:HGNC Symbol;Acc:HGNC:31628]"}, {"versioned_ensembl_gene_id":"ENSG00000200327.1","gene_symbol":"RNA5SP62","gene_name":"RNA, 5S ribosomal pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:42839]","synonyms":"RN5S62","biotype":"rRNA","ncbi_id":"100873297","summary":null,"start":163468496,"end":163468605,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:42839]"}, {"versioned_ensembl_gene_id":"ENSG00000242876.3","gene_symbol":"RN7SL812P","gene_name":"RNA, 7SL, cytoplasmic 812, pseudogene [Source:HGNC Symbol;Acc:HGNC:46828]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479518","summary":null,"start":20481935,"end":20482213,"strand":-1,"description":"RNA, 7SL, cytoplasmic 812, pseudogene [Source:HGNC Symbol;Acc:HGNC:46828]"}, {"versioned_ensembl_gene_id":"ENSG00000221455.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":92790453,"end":92790665,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000284387.1","gene_symbol":"MIR24-2","gene_name":"microRNA 24-2 [Source:HGNC Symbol;Acc:HGNC:31608]","synonyms":"MIRN24-2,hsa-mir-24-2","biotype":"miRNA","ncbi_id":"407013","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13836287,"end":13836359,"strand":-1,"description":"microRNA 24-2 [Source:HGNC Symbol;Acc:HGNC:31608]"}, {"versioned_ensembl_gene_id":"ENSG00000284268.1","gene_symbol":"MIR1181","gene_name":"microRNA 1181 [Source:HGNC Symbol;Acc:HGNC:35262]","synonyms":"MIRN1181,hsa-mir-1181","biotype":"miRNA","ncbi_id":"100302213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10403458,"end":10403538,"strand":-1,"description":"microRNA 1181 [Source:HGNC Symbol;Acc:HGNC:35262]"}, {"versioned_ensembl_gene_id":"ENSG00000273968.1","gene_symbol":"RN7SL105P","gene_name":"RNA, 7SL, cytoplasmic 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:46121]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480487","summary":null,"start":1604374,"end":1604672,"strand":-1,"description":"RNA, 7SL, cytoplasmic 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:46121]"}, {"versioned_ensembl_gene_id":"ENSG00000200370.1","gene_symbol":"RNA5S17","gene_name":"RNA, 5S ribosomal 17 [Source:HGNC Symbol;Acc:HGNC:34378]","synonyms":"RN5S17","biotype":"rRNA","ncbi_id":"100169768","summary":null,"start":228646040,"end":228646158,"strand":-1,"description":"RNA, 5S ribosomal 17 [Source:HGNC Symbol;Acc:HGNC:34378]"}, {"versioned_ensembl_gene_id":"ENSG00000200728.1","gene_symbol":"RNU6-271P","gene_name":"RNA, U6 small nuclear 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:47234]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481264","summary":null,"start":96112747,"end":96112851,"strand":1,"description":"RNA, U6 small nuclear 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:47234]"}, {"versioned_ensembl_gene_id":"ENSG00000266646.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31531364,"end":31531441,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000264047.2","gene_symbol":"RN7SL455P","gene_name":"RNA, 7SL, cytoplasmic 455, pseudogene [Source:HGNC Symbol;Acc:HGNC:46471]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479389","summary":null,"start":43904412,"end":43904693,"strand":1,"description":"RNA, 7SL, cytoplasmic 455, pseudogene [Source:HGNC Symbol;Acc:HGNC:46471]"}, {"versioned_ensembl_gene_id":"ENSG00000223111.1","gene_symbol":"SNORA74C-2","gene_name":"small nucleolar RNA, H/ACA box 74C-2 [Source:HGNC Symbol;Acc:HGNC:52218]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617009","summary":null,"start":49954214,"end":49954414,"strand":1,"description":"small nucleolar RNA, H/ACA box 74C-2 [Source:HGNC Symbol;Acc:HGNC:52218]"}, {"versioned_ensembl_gene_id":"ENSG00000252282.1","gene_symbol":"RNU6-1089P","gene_name":"RNA, U6 small nuclear 1089, pseudogene [Source:HGNC Symbol;Acc:HGNC:48052]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481523","summary":null,"start":245023015,"end":245023118,"strand":1,"description":"RNA, U6 small nuclear 1089, pseudogene [Source:HGNC Symbol;Acc:HGNC:48052]"}, {"versioned_ensembl_gene_id":"ENSG00000065833.8","gene_symbol":"ME1","gene_name":"malic enzyme 1 [Source:HGNC Symbol;Acc:HGNC:6983]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4199","summary":"This gene encodes a cytosolic, NADP-dependent enzyme that generates NADPH for fatty acid biosynthesis. The activity of this enzyme, the reversible oxidative decarboxylation of malate, links the glycolytic and citric acid cycles. The regulation of expression for this gene is complex. Increased expression can result from elevated levels of thyroid hormones or by higher proportions of carbohydrates in the diet. [provided by RefSeq, Jul 2008]","start":83210389,"end":83431071,"strand":-1,"description":"malic enzyme 1 [Source:HGNC Symbol;Acc:HGNC:6983]"}, {"versioned_ensembl_gene_id":"ENSG00000219951.4","gene_symbol":"AL391416.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83392416,"end":83393409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207625.1","gene_symbol":"MIR128-2","gene_name":"microRNA 128-2 [Source:HGNC Symbol;Acc:HGNC:31511]","synonyms":"MIRN128B,MIRN128-2,hsa-mir-128b,hsa-mir-128-2","biotype":"miRNA","ncbi_id":"406916","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35744476,"end":35744559,"strand":1,"description":"microRNA 128-2 [Source:HGNC Symbol;Acc:HGNC:31511]"}, {"versioned_ensembl_gene_id":"ENSG00000238669.1","gene_symbol":"RNU6-333P","gene_name":"RNA, U6 small nuclear 333, pseudogene [Source:HGNC Symbol;Acc:HGNC:47296]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480571","summary":null,"start":53138545,"end":53138651,"strand":-1,"description":"RNA, U6 small nuclear 333, pseudogene [Source:HGNC Symbol;Acc:HGNC:47296]"}, {"versioned_ensembl_gene_id":"ENSG00000199755.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67340068,"end":67340176,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263593.1","gene_symbol":"MIR4804","gene_name":"microRNA 4804 [Source:HGNC Symbol;Acc:HGNC:41720]","synonyms":"hsa-mir-4804","biotype":"miRNA","ncbi_id":"100616152","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72878591,"end":72878663,"strand":1,"description":"microRNA 4804 [Source:HGNC Symbol;Acc:HGNC:41720]"}, {"versioned_ensembl_gene_id":"ENSG00000266435.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32419522,"end":32419628,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000199568.1","gene_symbol":"RNU5A-1","gene_name":"RNA, U5A small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10211]","synonyms":"U5B1,U5A,RNU5C,RNU5A","biotype":"snRNA","ncbi_id":"26831","summary":null,"start":65296051,"end":65296166,"strand":1,"description":"RNA, U5A small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10211]"}, {"versioned_ensembl_gene_id":"ENSG00000240713.3","gene_symbol":"RN7SL860P","gene_name":"RNA, 7SL, cytoplasmic 860, pseudogene [Source:HGNC Symbol;Acc:HGNC:46876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106635537","summary":null,"start":22601485,"end":22601707,"strand":1,"description":"RNA, 7SL, cytoplasmic 860, pseudogene [Source:HGNC Symbol;Acc:HGNC:46876]"}, {"versioned_ensembl_gene_id":"ENSG00000284252.1","gene_symbol":"MIR4444-1","gene_name":"microRNA 4444-1 [Source:HGNC Symbol;Acc:HGNC:41710]","synonyms":"MIR4444,hsa-mir-4444","biotype":"miRNA","ncbi_id":"100616394","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177212726,"end":177212799,"strand":1,"description":"microRNA 4444-1 [Source:HGNC Symbol;Acc:HGNC:41710]"}, {"versioned_ensembl_gene_id":"ENSG00000284180.1","gene_symbol":"MIR3606","gene_name":"microRNA 3606 [Source:HGNC Symbol;Acc:HGNC:38881]","synonyms":"hsa-mir-3606","biotype":"miRNA","ncbi_id":"100500837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188995630,"end":188995692,"strand":1,"description":"microRNA 3606 [Source:HGNC Symbol;Acc:HGNC:38881]"}, {"versioned_ensembl_gene_id":"ENSG00000284544.1","gene_symbol":"MIR330","gene_name":"microRNA 330 [Source:HGNC Symbol;Acc:HGNC:31771]","synonyms":"MIRN330,hsa-mir-330","biotype":"miRNA","ncbi_id":"442902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45638994,"end":45639087,"strand":-1,"description":"microRNA 330 [Source:HGNC Symbol;Acc:HGNC:31771]"}, {"versioned_ensembl_gene_id":"ENSG00000165804.15","gene_symbol":"ZNF219","gene_name":"zinc finger protein 219 [Source:HGNC Symbol;Acc:HGNC:13011]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51222","summary":"This gene is a member of the Kruppel-like zinc finger gene family. The encoded protein functions as a transcriptional repressor of the high mobility group nucleosome binding domain 1 protein, which is associated with transcriptionally active chromatin. [provided by RefSeq, Apr 2017]","start":21090046,"end":21104722,"strand":-1,"description":"zinc finger protein 219 [Source:HGNC Symbol;Acc:HGNC:13011]"}, {"versioned_ensembl_gene_id":"ENSG00000232070.8","gene_symbol":"TMEM253","gene_name":"transmembrane protein 253 [Source:HGNC Symbol;Acc:HGNC:32545]","synonyms":"NCRNA00220,C14orf95,C14orf176","biotype":"protein_coding","ncbi_id":"643382","summary":null,"start":21098937,"end":21103724,"strand":1,"description":"transmembrane protein 253 [Source:HGNC Symbol;Acc:HGNC:32545]"}, {"versioned_ensembl_gene_id":"ENSG00000154898.15","gene_symbol":"CCDC144CP","gene_name":"coiled-coil domain containing 144C, pseudogene [Source:HGNC Symbol;Acc:HGNC:29073]","synonyms":"CCDC144C","biotype":"transcribed_processed_pseudogene","ncbi_id":"348254","summary":null,"start":20321164,"end":20403557,"strand":1,"description":"coiled-coil domain containing 144C, pseudogene [Source:HGNC Symbol;Acc:HGNC:29073]"}, {"versioned_ensembl_gene_id":"ENSG00000274620.1","gene_symbol":"MIR378J","gene_name":"microRNA 378j [Source:HGNC Symbol;Acc:HGNC:49979]","synonyms":"hsa-mir-378j","biotype":"miRNA","ncbi_id":"102465136","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37614931,"end":37615039,"strand":-1,"description":"microRNA 378j [Source:HGNC Symbol;Acc:HGNC:49979]"}, {"versioned_ensembl_gene_id":"ENSG00000278672.1","gene_symbol":"MIR8059","gene_name":"microRNA 8059 [Source:HGNC Symbol;Acc:HGNC:50068]","synonyms":"hsa-mir-8059","biotype":"miRNA","ncbi_id":"102466918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50768650,"end":50768730,"strand":1,"description":"microRNA 8059 [Source:HGNC Symbol;Acc:HGNC:50068]"}, {"versioned_ensembl_gene_id":"ENSG00000269906.1","gene_symbol":"AL606834.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50662511,"end":50663178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259113.1","gene_symbol":"AL118556.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50448807,"end":50456742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198513.11","gene_symbol":"ATL1","gene_name":"atlastin GTPase 1 [Source:HGNC Symbol;Acc:HGNC:11231]","synonyms":"SPG3,FSP1,AD-FSP,SPG3A","biotype":"protein_coding","ncbi_id":"51062","summary":"The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":50532509,"end":50633068,"strand":1,"description":"atlastin GTPase 1 [Source:HGNC Symbol;Acc:HGNC:11231]"}, {"versioned_ensembl_gene_id":"ENSG00000113161.15","gene_symbol":"HMGCR","gene_name":"3-hydroxy-3-methylglutaryl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:5006]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3156","summary":"HMG-CoA reductase is the rate-limiting enzyme for cholesterol synthesis and is regulated via a negative feedback mechanism mediated by sterols and non-sterol metabolites derived from mevalonate, the product of the reaction catalyzed by reductase. Normally in mammalian cells this enzyme is suppressed by cholesterol derived from the internalization and degradation of low density lipoprotein (LDL) via the LDL receptor. Competitive inhibitors of the reductase induce the expression of LDL receptors in the liver, which in turn increases the catabolism of plasma LDL and lowers the plasma concentration of cholesterol, an important determinant of atherosclerosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":75336329,"end":75362104,"strand":1,"description":"3-hydroxy-3-methylglutaryl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:5006]"}, {"versioned_ensembl_gene_id":"ENSG00000179038.8","gene_symbol":"AP001885.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":67195569,"end":67197167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061938.17","gene_symbol":"TNK2","gene_name":"tyrosine kinase non receptor 2 [Source:HGNC Symbol;Acc:HGNC:19297]","synonyms":"ACK,p21cdc42Hs,ACK1","biotype":"protein_coding","ncbi_id":"10188","summary":"This gene encodes a tyrosine kinase that binds Cdc42Hs in its GTP-bound form and inhibits both the intrinsic and GTPase-activating protein (GAP)-stimulated GTPase activity of Cdc42Hs. This binding is mediated by a unique sequence of 47 amino acids C-terminal to an SH3 domain. The protein may be involved in a regulatory mechanism that sustains the GTP-bound active form of Cdc42Hs and which is directly linked to a tyrosine phosphorylation signal transduction pathway. Several alternatively spliced transcript variants have been identified from this gene, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]","start":195863364,"end":195911945,"strand":-1,"description":"tyrosine kinase non receptor 2 [Source:HGNC Symbol;Acc:HGNC:19297]"}, {"versioned_ensembl_gene_id":"ENSG00000163531.15","gene_symbol":"NFASC","gene_name":"neurofascin [Source:HGNC Symbol;Acc:HGNC:29866]","synonyms":"NRCAML,NF,KIAA0756,FLJ46866","biotype":"protein_coding","ncbi_id":"23114","summary":"This gene encodes an L1 family immunoglobulin cell adhesion molecule with multiple IGcam and fibronectin domains. The protein functions in neurite outgrowth, neurite fasciculation, and organization of the axon initial segment (AIS) and nodes of Ranvier on axons during early development. Both the AIS and nodes of Ranvier contain high densities of voltage-gated Na+ (Nav) channels which are clustered by interactions with cytoskeletal and scaffolding proteins including this protein, gliomedin, ankyrin 3 (ankyrin-G), and betaIV spectrin. This protein links the AIS extracellular matrix to the intracellular cytoskeleton. This gene undergoes extensive alternative splicing, and the full-length nature of some variants has not been determined.[provided by RefSeq, May 2009]","start":204828651,"end":205022822,"strand":1,"description":"neurofascin [Source:HGNC Symbol;Acc:HGNC:29866]"}, {"versioned_ensembl_gene_id":"ENSG00000223966.1","gene_symbol":"AL159990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70726040,"end":70730856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176387.6","gene_symbol":"HSD11B2","gene_name":"hydroxysteroid 11-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5209]","synonyms":"SDR9C3","biotype":"protein_coding","ncbi_id":"3291","summary":"There are at least two isozymes of the corticosteroid 11-beta-dehydrogenase, a microsomal enzyme complex responsible for the interconversion of cortisol and cortisone. The type I isozyme has both 11-beta-dehydrogenase (cortisol to cortisone) and 11-oxoreductase (cortisone to cortisol) activities. The type II isozyme, encoded by this gene, has only 11-beta-dehydrogenase activity. In aldosterone-selective epithelial tissues such as the kidney, the type II isozyme catalyzes the glucocorticoid cortisol to the inactive metabolite cortisone, thus preventing illicit activation of the mineralocorticoid receptor. In tissues that do not express the mineralocorticoid receptor, such as the placenta and testis, it protects cells from the growth-inhibiting and/or pro-apoptotic effects of cortisol, particularly during embryonic development. Mutations in this gene cause the syndrome of apparent mineralocorticoid excess and hypertension. [provided by RefSeq, Feb 2010]","start":67430652,"end":67437553,"strand":1,"description":"hydroxysteroid 11-beta dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:5209]"}, {"versioned_ensembl_gene_id":"ENSG00000205786.8","gene_symbol":"LINC01531","gene_name":"long intergenic non-protein coding RNA 1531 [Source:HGNC Symbol;Acc:HGNC:51270]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128682","summary":null,"start":35399511,"end":35419385,"strand":1,"description":"long intergenic non-protein coding RNA 1531 [Source:HGNC Symbol;Acc:HGNC:51270]"}, {"versioned_ensembl_gene_id":"ENSG00000250866.1","gene_symbol":"AC022424.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5142138,"end":5176214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083067.22","gene_symbol":"TRPM3","gene_name":"transient receptor potential cation channel subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:17992]","synonyms":"LTRPC3,KIAA1616,GON-2","biotype":"protein_coding","ncbi_id":"80036","summary":"The product of this gene belongs to the family of transient receptor potential (TRP) channels. TRP channels are cation-selective channels important for cellular calcium signaling and homeostasis. The protein encoded by this gene mediates calcium entry, and this entry is potentiated by calcium store depletion. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":70529063,"end":71446904,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:17992]"}, {"versioned_ensembl_gene_id":"ENSG00000239223.3","gene_symbol":"AC026254.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27274107,"end":27274477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213664.4","gene_symbol":"AC026254.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27280482,"end":27280912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173599.13","gene_symbol":"PC","gene_name":"pyruvate carboxylase [Source:HGNC Symbol;Acc:HGNC:8636]","synonyms":"PCB","biotype":"protein_coding","ncbi_id":"5091","summary":"This gene encodes pyruvate carboxylase, which requires biotin and ATP to catalyse the carboxylation of pyruvate to oxaloacetate. The active enzyme is a homotetramer arranged in a tetrahedron which is located exclusively in the mitochondrial matrix. Pyruvate carboxylase is involved in gluconeogenesis, lipogenesis, insulin secretion and synthesis of the neurotransmitter glutamate. Mutations in this gene have been associated with pyruvate carboxylase deficiency. Alternatively spliced transcript variants with different 5' UTRs, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]","start":66848233,"end":66958376,"strand":-1,"description":"pyruvate carboxylase [Source:HGNC Symbol;Acc:HGNC:8636]"}, {"versioned_ensembl_gene_id":"ENSG00000100485.11","gene_symbol":"SOS2","gene_name":"SOS Ras/Rho guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:11188]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6655","summary":"This gene encodes a regulatory protein that is involved in the positive regulation of ras proteins. Mutations in this gene are associated with Noonan Syndrome-9. [provided by RefSeq, Jul 2016]","start":50117120,"end":50231558,"strand":-1,"description":"SOS Ras/Rho guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:11188]"}, {"versioned_ensembl_gene_id":"ENSG00000264431.1","gene_symbol":"AC131274.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22693325,"end":22694831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249865.1","gene_symbol":"AC027343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7367929,"end":7373074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227759.2","gene_symbol":"VTI1BP4","gene_name":"vesicle transport through interaction with t-SNAREs 1B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43730]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422540","summary":null,"start":128650998,"end":128652145,"strand":1,"description":"vesicle transport through interaction with t-SNAREs 1B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43730]"}, {"versioned_ensembl_gene_id":"ENSG00000249638.1","gene_symbol":"AC027343.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7362979,"end":7364531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273132.1","gene_symbol":"AL355312.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149852462,"end":149853192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236819.1","gene_symbol":"LINC01563","gene_name":"long intergenic non-protein coding RNA 1563 [Source:HGNC Symbol;Acc:HGNC:51343]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060544","summary":null,"start":21075556,"end":21090615,"strand":1,"description":"long intergenic non-protein coding RNA 1563 [Source:HGNC Symbol;Acc:HGNC:51343]"}, {"versioned_ensembl_gene_id":"ENSG00000108379.9","gene_symbol":"WNT3","gene_name":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]","synonyms":"MGC131950,INT4,MGC138323,MGC138321,MGC138323,MGC131950,MGC138321,INT4","biotype":"protein_coding","ncbi_id":"7473","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 98% amino acid identity to mouse Wnt3 protein, and 84% to human WNT3A protein, another WNT gene product. The mouse studies show the requirement of Wnt3 in primary axis formation in the mouse. Studies of the gene expression suggest that this gene may play a key role in some cases of human breast, rectal, lung, and gastric cancer through activation of the WNT-beta-catenin-TCF signaling pathway. This gene is clustered with WNT15, another family member, in the chromosome 17q21 region. [provided by RefSeq, Jul 2008]","start":46762506,"end":46833154,"strand":-1,"description":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]"}, {"versioned_ensembl_gene_id":"ENSG00000173261.8","gene_symbol":"PLAC8L1","gene_name":"PLAC8 like 1 [Source:HGNC Symbol;Acc:HGNC:31746]","synonyms":null,"biotype":"protein_coding","ncbi_id":"153770","summary":null,"start":146084386,"end":146104369,"strand":-1,"description":"PLAC8 like 1 [Source:HGNC Symbol;Acc:HGNC:31746]"}, {"versioned_ensembl_gene_id":"ENSG00000131408.13","gene_symbol":"NR1H2","gene_name":"nuclear receptor subfamily 1 group H member 2 [Source:HGNC Symbol;Acc:HGNC:7965]","synonyms":"UNR,RIP15,NER-I,NER,LXR-b","biotype":"protein_coding","ncbi_id":"7376","summary":"The liver X receptors, LXRA (NR1H3; MIM 602423) and LXRB, form a subfamily of the nuclear receptor superfamily and are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. The inducible LXRA is highly expressed in liver, adrenal gland, intestine, adipose tissue, macrophages, lung, and kidney, whereas LXRB is ubiquitously expressed. Ligand-activated LXRs form obligate heterodimers with retinoid X receptors (RXRs; see MIM 180245) and regulate expression of target genes containing LXR response elements (summary by Korf et al., 2009 [PubMed 19436111]).[supplied by OMIM, Jan 2010]","start":50329653,"end":50382982,"strand":1,"description":"nuclear receptor subfamily 1 group H member 2 [Source:HGNC Symbol;Acc:HGNC:7965]"}, {"versioned_ensembl_gene_id":"ENSG00000258381.1","gene_symbol":"AL512360.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48819360,"end":48819593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271153.1","gene_symbol":"RPL23AP88","gene_name":"ribosomal protein L23a pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:51579]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289034","summary":null,"start":242175181,"end":242175634,"strand":1,"description":"ribosomal protein L23a pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:51579]"}, {"versioned_ensembl_gene_id":"ENSG00000265556.1","gene_symbol":"LINC01984","gene_name":"long intergenic non-protein coding RNA 1984 [Source:HGNC Symbol;Acc:HGNC:52814]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107987252","summary":null,"start":20433206,"end":20434285,"strand":1,"description":"long intergenic non-protein coding RNA 1984 [Source:HGNC Symbol;Acc:HGNC:52814]"}, {"versioned_ensembl_gene_id":"ENSG00000235151.1","gene_symbol":"AC131097.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241844380,"end":241845036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278913.1","gene_symbol":"AC026797.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6134303,"end":6137171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250730.2","gene_symbol":"HMGB3P3","gene_name":"high mobility group box 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39102]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419949","summary":null,"start":6289857,"end":6290624,"strand":1,"description":"high mobility group box 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39102]"}, {"versioned_ensembl_gene_id":"ENSG00000123975.4","gene_symbol":"CKS2","gene_name":"CDC28 protein kinase regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:2000]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1164","summary":"CKS2 protein binds to the catalytic subunit of the cyclin dependent kinases and is essential for their biological function. The CKS2 mRNA is found to be expressed in different patterns through the cell cycle in HeLa cells, which reflects specialized role for the encoded protein. [provided by RefSeq, Jul 2008]","start":89311198,"end":89316703,"strand":1,"description":"CDC28 protein kinase regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:2000]"}, {"versioned_ensembl_gene_id":"ENSG00000232680.2","gene_symbol":"AC002511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35432957,"end":35434642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155506.16","gene_symbol":"LARP1","gene_name":"La ribonucleoprotein domain family member 1 [Source:HGNC Symbol;Acc:HGNC:29531]","synonyms":"KIAA0731,MGC19556,LARP","biotype":"protein_coding","ncbi_id":"23367","summary":null,"start":154712902,"end":154817607,"strand":1,"description":"La ribonucleoprotein domain family member 1 [Source:HGNC Symbol;Acc:HGNC:29531]"}, {"versioned_ensembl_gene_id":"ENSG00000281021.1","gene_symbol":"AL078581.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149576089,"end":149590864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205436.7","gene_symbol":"EXOC3L4","gene_name":"exocyst complex component 3 like 4 [Source:HGNC Symbol;Acc:HGNC:20120]","synonyms":"C14orf73","biotype":"protein_coding","ncbi_id":"91828","summary":null,"start":103100144,"end":103110559,"strand":1,"description":"exocyst complex component 3 like 4 [Source:HGNC Symbol;Acc:HGNC:20120]"}, {"versioned_ensembl_gene_id":"ENSG00000224945.1","gene_symbol":"AL353150.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89088604,"end":89109934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259444.1","gene_symbol":"AL161669.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":103094723,"end":103098885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145536.15","gene_symbol":"ADAMTS16","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 16 [Source:HGNC Symbol;Acc:HGNC:17108]","synonyms":"ADAMTS16s","biotype":"protein_coding","ncbi_id":"170690","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may inhibit chondrosarcoma cell proliferation and migration. This gene may regulate blood pressure. [provided by RefSeq, May 2016]","start":5140330,"end":5320304,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 16 [Source:HGNC Symbol;Acc:HGNC:17108]"}, {"versioned_ensembl_gene_id":"ENSG00000271871.1","gene_symbol":"AC005740.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141952419,"end":141953375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254039.1","gene_symbol":"AC027801.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49914403,"end":49932918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273314.1","gene_symbol":"AC005229.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148696467,"end":148698664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258602.1","gene_symbol":"LINC01629","gene_name":"long intergenic non-protein coding RNA 1629 [Source:HGNC Symbol;Acc:HGNC:52260]","synonyms":"linc-KIAA1737-2","biotype":"lincRNA","ncbi_id":"105370578","summary":null,"start":76959638,"end":76965802,"strand":1,"description":"long intergenic non-protein coding RNA 1629 [Source:HGNC Symbol;Acc:HGNC:52260]"}, {"versioned_ensembl_gene_id":"ENSG00000243225.2","gene_symbol":"AC007686.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76968683,"end":76969145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241081.1","gene_symbol":"AF111169.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76886377,"end":76886750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270200.1","gene_symbol":"AC005229.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148649547,"end":148650240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118705.16","gene_symbol":"RPN2","gene_name":"ribophorin II [Source:HGNC Symbol;Acc:HGNC:10382]","synonyms":"RIBIIR,SWP1,RPNII,RPN-II","biotype":"protein_coding","ncbi_id":"6185","summary":"This gene encodes a type I integral membrane protein found only in the rough endoplasmic reticulum. The encoded protein is part of an N-oligosaccharyl transferase complex that links high mannose oligosaccharides to asparagine residues found in the Asn-X-Ser/Thr consensus motif of nascent polypeptide chains. This protein is similar in sequence to the yeast oligosaccharyl transferase subunit SWP1. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":37178410,"end":37241623,"strand":1,"description":"ribophorin II [Source:HGNC Symbol;Acc:HGNC:10382]"}, {"versioned_ensembl_gene_id":"ENSG00000259508.1","gene_symbol":"AL132801.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102770040,"end":102774791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236159.1","gene_symbol":"AL031659.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37165774,"end":37166312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249215.1","gene_symbol":"NCOA4P4","gene_name":"nuclear receptor coactivator 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52405]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642262","summary":null,"start":139494256,"end":139496116,"strand":1,"description":"nuclear receptor coactivator 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52405]"}, {"versioned_ensembl_gene_id":"ENSG00000227671.4","gene_symbol":"AL390728.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":247189851,"end":247210856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179082.3","gene_symbol":"C9orf106","gene_name":"chromosome 9 open reading frame 106 [Source:HGNC Symbol;Acc:HGNC:31370]","synonyms":"bA65J3.5","biotype":"lincRNA","ncbi_id":"414318","summary":null,"start":129321016,"end":129324905,"strand":1,"description":"chromosome 9 open reading frame 106 [Source:HGNC Symbol;Acc:HGNC:31370]"}, {"versioned_ensembl_gene_id":"ENSG00000268615.1","gene_symbol":"AL353803.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129328261,"end":129328401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050130.17","gene_symbol":"JKAMP","gene_name":"JNK1/MAPK8-associated membrane protein [Source:HGNC Symbol;Acc:HGNC:20184]","synonyms":"JAMP,HSPC327,HSPC213,CDA06,C14orf100","biotype":"protein_coding","ncbi_id":"51528","summary":null,"start":59484443,"end":59505410,"strand":1,"description":"JNK1/MAPK8-associated membrane protein [Source:HGNC Symbol;Acc:HGNC:20184]"}, {"versioned_ensembl_gene_id":"ENSG00000204193.10","gene_symbol":"TXNDC8","gene_name":"thioredoxin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:31454]","synonyms":"TRX6,SPTRX-3,bA427L11.2","biotype":"protein_coding","ncbi_id":"255220","summary":null,"start":110303521,"end":110337884,"strand":-1,"description":"thioredoxin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:31454]"}, {"versioned_ensembl_gene_id":"ENSG00000130559.18","gene_symbol":"CAMSAP1","gene_name":"calmodulin regulated spectrin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:19946]","synonyms":"FLJ31228,DKFZp434F195","biotype":"protein_coding","ncbi_id":"157922","summary":null,"start":135808487,"end":135907228,"strand":-1,"description":"calmodulin regulated spectrin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:19946]"}, {"versioned_ensembl_gene_id":"ENSG00000267679.1","gene_symbol":"EIF5AP2","gene_name":"eukaryotic translation initiation factor 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3303]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1986","summary":null,"start":78157403,"end":78159135,"strand":1,"description":"eukaryotic translation initiation factor 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3303]"}, {"versioned_ensembl_gene_id":"ENSG00000100565.15","gene_symbol":"LRRC74A","gene_name":"leucine rich repeat containing 74A [Source:HGNC Symbol;Acc:HGNC:23346]","synonyms":"LRRC74,C14orf166B","biotype":"protein_coding","ncbi_id":"145497","summary":null,"start":76826372,"end":76870302,"strand":1,"description":"leucine rich repeat containing 74A [Source:HGNC Symbol;Acc:HGNC:23346]"}, {"versioned_ensembl_gene_id":"ENSG00000099337.4","gene_symbol":"KCNK6","gene_name":"potassium two pore domain channel subfamily K member 6 [Source:HGNC Symbol;Acc:HGNC:6281]","synonyms":"TWIK-2,K2p6.1","biotype":"protein_coding","ncbi_id":"9424","summary":"This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. This channel protein, considered an open rectifier, is widely expressed. It is stimulated by arachidonic acid, and inhibited by internal acidification and volatile anaesthetics. [provided by RefSeq, Jul 2008]","start":38319844,"end":38332076,"strand":1,"description":"potassium two pore domain channel subfamily K member 6 [Source:HGNC Symbol;Acc:HGNC:6281]"}, {"versioned_ensembl_gene_id":"ENSG00000279095.1","gene_symbol":"AC243964.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44664131,"end":44666158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107672.14","gene_symbol":"NSMCE4A","gene_name":"NSE4 homolog A, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:25935]","synonyms":"NSE4A,FLJ20003,C10orf86,bA500G22.3","biotype":"protein_coding","ncbi_id":"54780","summary":null,"start":121957088,"end":121975217,"strand":-1,"description":"NSE4 homolog A, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:25935]"}, {"versioned_ensembl_gene_id":"ENSG00000234982.1","gene_symbol":"AL441963.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14204248,"end":14205039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266903.1","gene_symbol":"AC243964.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44632199,"end":44718759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126583.10","gene_symbol":"PRKCG","gene_name":"protein kinase C gamma [Source:HGNC Symbol;Acc:HGNC:9402]","synonyms":"SCA14,PKCG,PKCC,MGC57564","biotype":"protein_coding","ncbi_id":"5582","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":53879190,"end":53907652,"strand":1,"description":"protein kinase C gamma [Source:HGNC Symbol;Acc:HGNC:9402]"}, {"versioned_ensembl_gene_id":"ENSG00000149218.4","gene_symbol":"ENDOD1","gene_name":"endonuclease domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29129]","synonyms":"KIAA0830","biotype":"protein_coding","ncbi_id":"23052","summary":null,"start":95089810,"end":95132645,"strand":1,"description":"endonuclease domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29129]"}, {"versioned_ensembl_gene_id":"ENSG00000255458.5","gene_symbol":"AC108471.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39639140,"end":39666644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249061.1","gene_symbol":"AC109492.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86967321,"end":87137712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258583.5","gene_symbol":"LINC01500","gene_name":"long intergenic non-protein coding RNA 1500 [Source:HGNC Symbol;Acc:HGNC:51166]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723742","summary":null,"start":58828234,"end":59017328,"strand":1,"description":"long intergenic non-protein coding RNA 1500 [Source:HGNC Symbol;Acc:HGNC:51166]"}, {"versioned_ensembl_gene_id":"ENSG00000109846.7","gene_symbol":"CRYAB","gene_name":"crystallin alpha B [Source:HGNC Symbol;Acc:HGNC:2389]","synonyms":"HSPB5,CRYA2","biotype":"protein_coding","ncbi_id":"1410","summary":"Mammalian lens crystallins are divided into alpha, beta, and gamma families. Alpha crystallins are composed of two gene products: alpha-A and alpha-B, for acidic and basic, respectively. Alpha crystallins can be induced by heat shock and are members of the small heat shock protein (HSP20) family. They act as molecular chaperones although they do not renature proteins and release them in the fashion of a true chaperone; instead they hold them in large soluble aggregates. These heterogeneous aggregates consist of 30-40 subunits; the alpha-A and alpha-B subunits have a 3:1 ratio, respectively. Two additional functions of alpha crystallins are an autokinase activity and participation in the intracellular architecture. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alpha-A and alpha-B gene products are differentially expressed; alpha-A is preferentially restricted to the lens and alpha-B is expressed widely in many tissues and organs. Elevated expression of alpha-B crystallin occurs in many neurological diseases; a missense mutation cosegregated in a family with a desmin-related myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2019]","start":111908565,"end":111923722,"strand":-1,"description":"crystallin alpha B [Source:HGNC Symbol;Acc:HGNC:2389]"}, {"versioned_ensembl_gene_id":"ENSG00000144191.11","gene_symbol":"CNGA3","gene_name":"cyclic nucleotide gated channel alpha 3 [Source:HGNC Symbol;Acc:HGNC:2150]","synonyms":"CNCG3,CCNCa,CCNC1,ACHM2,CNG3","biotype":"protein_coding","ncbi_id":"1261","summary":"This gene encodes a member of the cyclic nucleotide-gated cation channel protein family which is required for normal vision and olfactory signal transduction. Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness. Two alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":98346155,"end":98398601,"strand":1,"description":"cyclic nucleotide gated channel alpha 3 [Source:HGNC Symbol;Acc:HGNC:2150]"}, {"versioned_ensembl_gene_id":"ENSG00000135747.11","gene_symbol":"ZNF670-ZNF695","gene_name":"ZNF670-ZNF695 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533111","summary":"This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 670 (ZNF670) and zinc finger protein 695 (ZNF695) genes on chromosome 1. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":246945547,"end":247078811,"strand":-1,"description":"ZNF670-ZNF695 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49200]"}, {"versioned_ensembl_gene_id":"ENSG00000255703.1","gene_symbol":"AC127070.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132899984,"end":132900368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135604.9","gene_symbol":"STX11","gene_name":"syntaxin 11 [Source:HGNC Symbol;Acc:HGNC:11429]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8676","summary":"This gene encodes a member of the syntaxin family. Syntaxins have been implicated in the targeting and fusion of intracellular transport vesicles. This family member may regulate protein transport among late endosomes and the trans-Golgi network. Mutations in this gene have been associated with familial hemophagocytic lymphohistiocytosis. [provided by RefSeq, Jul 2008]","start":144150526,"end":144188370,"strand":1,"description":"syntaxin 11 [Source:HGNC Symbol;Acc:HGNC:11429]"}, {"versioned_ensembl_gene_id":"ENSG00000229738.1","gene_symbol":"AC010240.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132987652,"end":132988110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168398.6","gene_symbol":"BDKRB2","gene_name":"bradykinin receptor B2 [Source:HGNC Symbol;Acc:HGNC:1030]","synonyms":"BK-2","biotype":"protein_coding","ncbi_id":"624","summary":"This gene encodes a receptor for bradykinin. The 9 aa bradykinin peptide elicits many responses including vasodilation, edema, smooth muscle spasm and pain fiber stimulation. Bradykinin is released upon activation by pathophysiologic conditions such as trauma and inflammation, and binds to its kinin receptors, B1 and B2. The B2 receptor associates with G proteins that stimulate a phosphatidylinositol-calcium second messenger system. [provided by RefSeq, Apr 2020]","start":96204679,"end":96244166,"strand":1,"description":"bradykinin receptor B2 [Source:HGNC Symbol;Acc:HGNC:1030]"}, {"versioned_ensembl_gene_id":"ENSG00000251585.1","gene_symbol":"AC026444.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86402465,"end":86402960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227681.5","gene_symbol":"AL033504.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147660703,"end":147953937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100380.13","gene_symbol":"ST13","gene_name":"ST13, Hsp70 interacting protein [Source:HGNC Symbol;Acc:HGNC:11343]","synonyms":"HIP,FAM10A1,SNC6,P48,HSPABP1","biotype":"protein_coding","ncbi_id":"6767","summary":"The protein encoded by this gene is an adaptor protein that mediates the association of the heat shock proteins HSP70 and HSP90. This protein has been shown to be involved in the assembly process of glucocorticoid receptor, which requires the assistance of multiple molecular chaperones. The expression of this gene is reported to be downregulated in colorectal carcinoma tissue suggesting that it is a candidate tumor suppressor gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]","start":40824535,"end":40857022,"strand":-1,"description":"ST13, Hsp70 interacting protein [Source:HGNC Symbol;Acc:HGNC:11343]"}, {"versioned_ensembl_gene_id":"ENSG00000130312.6","gene_symbol":"MRPL34","gene_name":"mitochondrial ribosomal protein L34 [Source:HGNC Symbol;Acc:HGNC:14488]","synonyms":"MGC2633,MGC24974,L34mt","biotype":"protein_coding","ncbi_id":"64981","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":17292609,"end":17306843,"strand":1,"description":"mitochondrial ribosomal protein L34 [Source:HGNC Symbol;Acc:HGNC:14488]"}, {"versioned_ensembl_gene_id":"ENSG00000242952.1","gene_symbol":"RPSAP3","gene_name":"ribosomal protein SA pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19792]","synonyms":"LAMR1P3","biotype":"transcribed_processed_pseudogene","ncbi_id":"158674","summary":null,"start":76634775,"end":76635661,"strand":-1,"description":"ribosomal protein SA pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:19792]"}, {"versioned_ensembl_gene_id":"ENSG00000253713.1","gene_symbol":"AC091819.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167116318,"end":167119585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229119.3","gene_symbol":"AC026403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166382305,"end":166382599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260103.2","gene_symbol":"AC012435.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":74478070,"end":74490286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267246.1","gene_symbol":"AC091132.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45549781,"end":45558738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272832.1","gene_symbol":"AC022296.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133543064,"end":133543466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101342.9","gene_symbol":"TLDC2","gene_name":"TBC/LysM-associated domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16112]","synonyms":"C20orf118,dJ132F21.2","biotype":"protein_coding","ncbi_id":"140711","summary":null,"start":36876121,"end":36894235,"strand":1,"description":"TBC/LysM-associated domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16112]"}, {"versioned_ensembl_gene_id":"ENSG00000161647.18","gene_symbol":"MPP3","gene_name":"membrane palmitoylated protein 3 [Source:HGNC Symbol;Acc:HGNC:7221]","synonyms":"DLG3","biotype":"protein_coding","ncbi_id":"4356","summary":"This gene product is a member of a family of membrane-associated proteins termed MAGUKs (membrane-associated guanylate kinase homologs). MAGUKs interact with the cytoskeleton and regulate cell proliferation, signaling pathways, and intracellular junctions. This protein contains a conserved sequence, called the SH3 (src homology 3) motif, found in several other proteins that associate with the cytoskeleton and are suspected to play important roles in signal transduction. Alternatively spliced transcript variants have been identified. One transcript variant is experimentally supported, but it doesn't encode a protein. [provided by RefSeq, Jul 2008]","start":43800799,"end":43833170,"strand":-1,"description":"membrane palmitoylated protein 3 [Source:HGNC Symbol;Acc:HGNC:7221]"}, {"versioned_ensembl_gene_id":"ENSG00000070526.14","gene_symbol":"ST6GALNAC1","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23614]","synonyms":"ST6GalNAcI,SIAT7A","biotype":"protein_coding","ncbi_id":"55808","summary":"Glycosylation of proteins affects cell-cell interaction, interactions with the matrix, and the functions of intracellular molecules. ST6GALNAC1 transfers a sialic acid, N-acetylneuraminic acid (NeuAc), in an alpha-2,6 linkage to O-linked GalNAc residues. The cancer-associated sialyl-Tn (sTn) antigen is formed by ST6GALNAC1-catalyzed sialylation of GalNAc residues on mucins (Ikehara et al., 1999 [PubMed 10536037]; Sewell et al., 2006 [PubMed 16319059]).[supplied by OMIM, Mar 2008]","start":76624761,"end":76643838,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23614]"}, {"versioned_ensembl_gene_id":"ENSG00000224302.1","gene_symbol":"AL500527.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102085476,"end":102085730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004779.9","gene_symbol":"NDUFAB1","gene_name":"NADH:ubiquinone oxidoreductase subunit AB1 [Source:HGNC Symbol;Acc:HGNC:7694]","synonyms":"SDAP,FASN2A,ACP1,ACP","biotype":"protein_coding","ncbi_id":"4706","summary":null,"start":23581002,"end":23596356,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit AB1 [Source:HGNC Symbol;Acc:HGNC:7694]"}, {"versioned_ensembl_gene_id":"ENSG00000168685.14","gene_symbol":"IL7R","gene_name":"interleukin 7 receptor [Source:HGNC Symbol;Acc:HGNC:6024]","synonyms":"CD127","biotype":"protein_coding","ncbi_id":"3575","summary":"The protein encoded by this gene is a receptor for interleukin 7 (IL7). The function of this receptor requires the interleukin 2 receptor, gamma chain (IL2RG), which is a common gamma chain shared by the receptors of various cytokines, including interleukins 2, 4, 7, 9, and 15. This protein has been shown to play a critical role in V(D)J recombination during lymphocyte development. Defects in this gene may be associated with severe combined immunodeficiency (SCID). Alternatively spliced transcript variants have been found. [provided by RefSeq, Dec 2015]","start":35852695,"end":35879603,"strand":1,"description":"interleukin 7 receptor [Source:HGNC Symbol;Acc:HGNC:6024]"}, {"versioned_ensembl_gene_id":"ENSG00000273877.4","gene_symbol":"AC236972.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153225649,"end":153230357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284635.1","gene_symbol":"AC093762.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":227745845,"end":227746681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226718.1","gene_symbol":"SNRPGP8","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39327]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874409","summary":null,"start":227778510,"end":227778735,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39327]"}, {"versioned_ensembl_gene_id":"ENSG00000164405.10","gene_symbol":"UQCRQ","gene_name":"ubiquinol-cytochrome c reductase complex III subunit VII [Source:HGNC Symbol;Acc:HGNC:29594]","synonyms":"UQCR7,QP-C,QCR8","biotype":"protein_coding","ncbi_id":"27089","summary":"This gene encodes a ubiquinone-binding protein of low molecular mass. This protein is a small core-associated protein and a subunit of ubiquinol-cytochrome c reductase complex III, which is part of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2008]","start":132866560,"end":132868031,"strand":1,"description":"ubiquinol-cytochrome c reductase complex III subunit VII [Source:HGNC Symbol;Acc:HGNC:29594]"}, {"versioned_ensembl_gene_id":"ENSG00000188729.6","gene_symbol":"OSTN","gene_name":"osteocrin [Source:HGNC Symbol;Acc:HGNC:29961]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344901","summary":null,"start":191199241,"end":191265615,"strand":1,"description":"osteocrin [Source:HGNC Symbol;Acc:HGNC:29961]"}, {"versioned_ensembl_gene_id":"ENSG00000214140.10","gene_symbol":"PRCD","gene_name":"photoreceptor disc component [Source:HGNC Symbol;Acc:HGNC:32528]","synonyms":"RP36","biotype":"protein_coding","ncbi_id":"768206","summary":"This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]","start":76527586,"end":76553578,"strand":1,"description":"photoreceptor disc component [Source:HGNC Symbol;Acc:HGNC:32528]"}, {"versioned_ensembl_gene_id":"ENSG00000080815.18","gene_symbol":"PSEN1","gene_name":"presenilin 1 [Source:HGNC Symbol;Acc:HGNC:9508]","synonyms":"S182,PS1,FAD,AD3","biotype":"protein_coding","ncbi_id":"5663","summary":"Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1; PSEN2) or in the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor, such that they either directly regulate gamma-secretase activity or themselves are protease enzymes. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene, the full-length nature of only some have been determined. [provided by RefSeq, Aug 2008]","start":73136418,"end":73223691,"strand":1,"description":"presenilin 1 [Source:HGNC Symbol;Acc:HGNC:9508]"}, {"versioned_ensembl_gene_id":"ENSG00000163683.11","gene_symbol":"SMIM14","gene_name":"small integral membrane protein 14 [Source:HGNC Symbol;Acc:HGNC:27321]","synonyms":"FLJ13289,C4orf34","biotype":"protein_coding","ncbi_id":"201895","summary":null,"start":39546330,"end":39639090,"strand":-1,"description":"small integral membrane protein 14 [Source:HGNC Symbol;Acc:HGNC:27321]"}, {"versioned_ensembl_gene_id":"ENSG00000104894.11","gene_symbol":"CD37","gene_name":"CD37 molecule [Source:HGNC Symbol;Acc:HGNC:1666]","synonyms":"TSPAN26","biotype":"protein_coding","ncbi_id":"951","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins and other transmembrane 4 superfamily proteins. It may play a role in T-cell-B-cell interactions. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":49335171,"end":49343335,"strand":1,"description":"CD37 molecule [Source:HGNC Symbol;Acc:HGNC:1666]"}, {"versioned_ensembl_gene_id":"ENSG00000268157.1","gene_symbol":"AC010524.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49356152,"end":49357769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134802.17","gene_symbol":"SLC43A3","gene_name":"solute carrier family 43 member 3 [Source:HGNC Symbol;Acc:HGNC:17466]","synonyms":"SEEEG-1,PRO1659,FOAP-13,Eeg1,DKFZp762A227","biotype":"protein_coding","ncbi_id":"29015","summary":null,"start":57406954,"end":57427580,"strand":-1,"description":"solute carrier family 43 member 3 [Source:HGNC Symbol;Acc:HGNC:17466]"}, {"versioned_ensembl_gene_id":"ENSG00000269560.1","gene_symbol":"AC010422.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12529768,"end":12532973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180855.15","gene_symbol":"ZNF443","gene_name":"zinc finger protein 443 [Source:HGNC Symbol;Acc:HGNC:20878]","synonyms":"ZK1","biotype":"protein_coding","ncbi_id":"10224","summary":"Zinc finger proteins (ZNFs) bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. For a general description of these proteins, see ZNF91 (MIM 603971).[supplied by OMIM, Jul 2002]","start":12429707,"end":12441112,"strand":-1,"description":"zinc finger protein 443 [Source:HGNC Symbol;Acc:HGNC:20878]"}, {"versioned_ensembl_gene_id":"ENSG00000091428.17","gene_symbol":"RAPGEF4","gene_name":"Rap guanine nucleotide exchange factor 4 [Source:HGNC Symbol;Acc:HGNC:16626]","synonyms":"cAMP-GEFII,CGEF2","biotype":"protein_coding","ncbi_id":"11069","summary":null,"start":172735274,"end":173052893,"strand":1,"description":"Rap guanine nucleotide exchange factor 4 [Source:HGNC Symbol;Acc:HGNC:16626]"}, {"versioned_ensembl_gene_id":"ENSG00000141744.3","gene_symbol":"PNMT","gene_name":"phenylethanolamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:9160]","synonyms":"PENT","biotype":"protein_coding","ncbi_id":"5409","summary":"The product of this gene catalyzes the last step of the catecholamine biosynthesis pathway, which methylates norepinephrine to form epinephrine (adrenaline). The enzyme also has beta-carboline 2N-methyltransferase activity. This gene is thought to play a key step in regulating epinephrine production. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2012]","start":39667981,"end":39670475,"strand":1,"description":"phenylethanolamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:9160]"}, {"versioned_ensembl_gene_id":"ENSG00000253209.1","gene_symbol":"IGHV3-65","gene_name":"immunoglobulin heavy variable 3-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5618]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28413","summary":null,"start":106666092,"end":106666532,"strand":-1,"description":"immunoglobulin heavy variable 3-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5618]"}, {"versioned_ensembl_gene_id":"ENSG00000089060.11","gene_symbol":"SLC8B1","gene_name":"solute carrier family 8 member B1 [Source:HGNC Symbol;Acc:HGNC:26175]","synonyms":"SLC24A6,NCLX,NCKX6,FLJ22233","biotype":"protein_coding","ncbi_id":"80024","summary":"SLC24A6 belongs to a family of potassium-dependent sodium/calcium exchangers that maintain cellular calcium homeostasis through the electrogenic countertransport of 4 sodium ions for 1 calcium ion and 1 potassium ion (Cai and Lytton, 2004 [PubMed 14625281]).[supplied by OMIM, Mar 2008]","start":113298759,"end":113359493,"strand":-1,"description":"solute carrier family 8 member B1 [Source:HGNC Symbol;Acc:HGNC:26175]"}, {"versioned_ensembl_gene_id":"ENSG00000258467.1","gene_symbol":"AL132857.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36533506,"end":36534538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224931.3","gene_symbol":"AC152010.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153122145,"end":153128323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253563.2","gene_symbol":"NKX2-1-AS1","gene_name":"NKX2-1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40585]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506237","summary":null,"start":36519278,"end":36523016,"strand":1,"description":"NKX2-1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40585]"}, {"versioned_ensembl_gene_id":"ENSG00000169436.16","gene_symbol":"COL22A1","gene_name":"collagen type XXII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22989]","synonyms":null,"biotype":"protein_coding","ncbi_id":"169044","summary":"This gene encodes member of the collagen family which is thought to contribute to the stabilization of myotendinous junctions and strengthen skeletal muscle attachments during contractile activity. It belongs to the fibril-associated collagens with interrupted triple helix (FACIT) subset of the collagen superfamily, which associate with collagen fibers through their C-terminal collagenous domains and mediate protein-protein interactions through their N-terminal noncollagenous domains. The encoded protein is deposited in the basement membrane zone of the myotendinous junction which is present only at the tissue junctions of muscles, tendons, the heart, articular cartilage, and skin. A knockdown of the orthologous zebrafish gene induces a muscular dystrophy by disruption of the myotendinous junction. [provided by RefSeq, May 2017]","start":138588235,"end":138914006,"strand":-1,"description":"collagen type XXII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22989]"}, {"versioned_ensembl_gene_id":"ENSG00000254682.1","gene_symbol":"AP002387.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71448674,"end":71452157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233493.3","gene_symbol":"TMEM238","gene_name":"transmembrane protein 238 [Source:HGNC Symbol;Acc:HGNC:40042]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388564","summary":null,"start":55379245,"end":55384598,"strand":-1,"description":"transmembrane protein 238 [Source:HGNC Symbol;Acc:HGNC:40042]"}, {"versioned_ensembl_gene_id":"ENSG00000269275.1","gene_symbol":"AC020922.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55377579,"end":55378125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080823.22","gene_symbol":"MOK","gene_name":"MOK protein kinase [Source:HGNC Symbol;Acc:HGNC:9833]","synonyms":"STK30,RAGE1,RAGE","biotype":"protein_coding","ncbi_id":"5891","summary":"This gene belongs to the MAP kinase superfamily. The gene was found to be regulated by caudal type transcription factor 2 (Cdx2) protein. The encoded protein, which is localized to epithelial cells in the intestinal crypt, may play a role in growth arrest and differentiation of cells of upper crypt and lower villus regions. Multiple alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Dec 2012]","start":102224500,"end":102305200,"strand":-1,"description":"MOK protein kinase [Source:HGNC Symbol;Acc:HGNC:9833]"}, {"versioned_ensembl_gene_id":"ENSG00000235371.1","gene_symbol":"AL122018.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":236110061,"end":236112370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120727.12","gene_symbol":"PAIP2","gene_name":"poly(A) binding protein interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17970]","synonyms":"PAIP2A","biotype":"protein_coding","ncbi_id":"51247","summary":null,"start":139341587,"end":139369720,"strand":1,"description":"poly(A) binding protein interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17970]"}, {"versioned_ensembl_gene_id":"ENSG00000167523.13","gene_symbol":"SPATA33","gene_name":"spermatogenesis associated 33 [Source:HGNC Symbol;Acc:HGNC:26463]","synonyms":"FLJ31606,C16orf55","biotype":"protein_coding","ncbi_id":"124045","summary":null,"start":89657802,"end":89671272,"strand":1,"description":"spermatogenesis associated 33 [Source:HGNC Symbol;Acc:HGNC:26463]"}, {"versioned_ensembl_gene_id":"ENSG00000185986.11","gene_symbol":"SDHAP3","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18781]","synonyms":"SDHAL,SDHACL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728609","summary":null,"start":1572222,"end":1594620,"strand":-1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18781]"}, {"versioned_ensembl_gene_id":"ENSG00000251532.1","gene_symbol":"AC091849.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1544107,"end":1551710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100372.14","gene_symbol":"SLC25A17","gene_name":"solute carrier family 25 member 17 [Source:HGNC Symbol;Acc:HGNC:10987]","synonyms":"PMP34","biotype":"protein_coding","ncbi_id":"10478","summary":"This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":40769630,"end":40819399,"strand":-1,"description":"solute carrier family 25 member 17 [Source:HGNC Symbol;Acc:HGNC:10987]"}, {"versioned_ensembl_gene_id":"ENSG00000269009.1","gene_symbol":"SLC6A21P","gene_name":"solute carrier family 6 member 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:31400]","synonyms":"SLC6A21","biotype":"processed_pseudogene","ncbi_id":"652969","summary":null,"start":49255472,"end":49256102,"strand":-1,"description":"solute carrier family 6 member 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:31400]"}, {"versioned_ensembl_gene_id":"ENSG00000247092.6","gene_symbol":"SNHG10","gene_name":"small nucleolar RNA host gene 10 [Source:HGNC Symbol;Acc:HGNC:27510]","synonyms":"NCRNA00063,LINC00063,FLJ40557,C14orf62","biotype":"antisense_RNA","ncbi_id":"283596","summary":"This gene is small nucleolar RNA host gene 10 and represents a non-protein coding RNA. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]","start":95532297,"end":95534872,"strand":-1,"description":"small nucleolar RNA host gene 10 [Source:HGNC Symbol;Acc:HGNC:27510]"}, {"versioned_ensembl_gene_id":"ENSG00000228218.1","gene_symbol":"ATF4P3","gene_name":"activating transcription factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:788]","synonyms":"ATF4C","biotype":"processed_pseudogene","ncbi_id":"643159","summary":null,"start":76225751,"end":76226806,"strand":-1,"description":"activating transcription factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:788]"}, {"versioned_ensembl_gene_id":"ENSG00000267128.1","gene_symbol":"RNF157-AS1","gene_name":"RNF157 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44127]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507218","summary":null,"start":76140556,"end":76154650,"strand":1,"description":"RNF157 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44127]"}, {"versioned_ensembl_gene_id":"ENSG00000144452.14","gene_symbol":"ABCA12","gene_name":"ATP binding cassette subfamily A member 12 [Source:HGNC Symbol;Acc:HGNC:14637]","synonyms":"LI2,ICR2B,DKFZP434G232","biotype":"protein_coding","ncbi_id":"26154","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily, which is the only major ABC subfamily found exclusively in multicellular eukaryotes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":214931542,"end":215138428,"strand":-1,"description":"ATP binding cassette subfamily A member 12 [Source:HGNC Symbol;Acc:HGNC:14637]"}, {"versioned_ensembl_gene_id":"ENSG00000227769.7","gene_symbol":"AC072062.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":215004782,"end":215085488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279382.1","gene_symbol":"AC018665.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76090308,"end":76091669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000014641.17","gene_symbol":"MDH1","gene_name":"malate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:6970]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4190","summary":"This gene encodes an enzyme that catalyzes the NAD/NADH-dependent, reversible oxidation of malate to oxaloacetate in many metabolic pathways, including the citric acid cycle. Two main isozymes are known to exist in eukaryotic cells: one is found in the mitochondrial matrix and the other in the cytoplasm. This gene encodes the cytosolic isozyme, which plays a key role in the malate-aspartate shuttle that allows malate to pass through the mitochondrial membrane to be transformed into oxaloacetate for further cellular processes. Alternatively spliced transcript variants have been found for this gene. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Pseudogenes have been identified on chromosomes X and 6. [provided by RefSeq, Feb 2016]","start":63588609,"end":63607197,"strand":1,"description":"malate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:6970]"}, {"versioned_ensembl_gene_id":"ENSG00000160999.10","gene_symbol":"SH2B2","gene_name":"SH2B adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:17381]","synonyms":"APS","biotype":"protein_coding","ncbi_id":"10603","summary":"The protein encoded by this gene is expressed in B lymphocytes and contains pleckstrin homology and src homology 2 (SH2) domains. In Burkitt's lymphoma cell lines, it is tyrosine-phosphorylated in response to B cell receptor stimulation. Because it binds Shc independent of stimulation and Grb2 after stimulation, it appears to play a role in signal transduction from the receptor to the Shc/Grb2 pathway. [provided by RefSeq, Jun 2009]","start":102285091,"end":102321711,"strand":1,"description":"SH2B adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:17381]"}, {"versioned_ensembl_gene_id":"ENSG00000226631.1","gene_symbol":"SLC9A3P3","gene_name":"solute carrier family 9 member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33492]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728990","summary":null,"start":50025135,"end":50027363,"strand":-1,"description":"solute carrier family 9 member 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33492]"}, {"versioned_ensembl_gene_id":"ENSG00000182473.21","gene_symbol":"EXOC7","gene_name":"exocyst complex component 7 [Source:HGNC Symbol;Acc:HGNC:23214]","synonyms":"YJL085W,KIAA1067,Exo70p,EXO70","biotype":"protein_coding","ncbi_id":"23265","summary":"The protein encoded by this gene is a component of the exocyst complex. The exocyst complex plays a critical role in vesicular trafficking and the secretory pathway by targeting post-Golgi vesicles to the plasma membrane. The encoded protein is required for assembly of the exocyst complex and docking of the complex to the plasma membrane. The encoded protein may also play a role in pre-mRNA splicing through interactions with pre-mRNA-processing factor 19. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Nov 2011]","start":76081017,"end":76121576,"strand":-1,"description":"exocyst complex component 7 [Source:HGNC Symbol;Acc:HGNC:23214]"}, {"versioned_ensembl_gene_id":"ENSG00000229776.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480730","summary":null,"start":32032713,"end":32036258,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000279333.1","gene_symbol":"AC096636.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":210678315,"end":210681932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181282.4","gene_symbol":"OR5AK3P","gene_name":"olfactory receptor family 5 subfamily AK member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15252]","synonyms":"OR5AK3","biotype":"unprocessed_pseudogene","ncbi_id":"81228","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56970850,"end":56972146,"strand":1,"description":"olfactory receptor family 5 subfamily AK member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15252]"}, {"versioned_ensembl_gene_id":"ENSG00000113328.18","gene_symbol":"CCNG1","gene_name":"cyclin G1 [Source:HGNC Symbol;Acc:HGNC:1592]","synonyms":"CCNG","biotype":"protein_coding","ncbi_id":"900","summary":"The eukaryotic cell cycle is governed by cyclin-dependent protein kinases (CDKs) whose activities are regulated by cyclins and CDK inhibitors. The protein encoded by this gene is a member of the cyclin family and contains the cyclin box. The encoded protein lacks the protein destabilizing (PEST) sequence that is present in other family members. Transcriptional activation of this gene can be induced by tumor protein p53. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":163437569,"end":163446151,"strand":1,"description":"cyclin G1 [Source:HGNC Symbol;Acc:HGNC:1592]"}, {"versioned_ensembl_gene_id":"ENSG00000109670.13","gene_symbol":"FBXW7","gene_name":"F-box and WD repeat domain containing 7 [Source:HGNC Symbol;Acc:HGNC:16712]","synonyms":"FBW7,CDC4,AGO,SEL10,SEL-10,FLJ11071,FBXW6,FBX30","biotype":"protein_coding","ncbi_id":"55294","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene was previously referred to as FBX30, and belongs to the Fbws class; in addition to an F-box, this protein contains 7 tandem WD40 repeats. This protein binds directly to cyclin E and probably targets cyclin E for ubiquitin-mediated degradation. Mutations in this gene are detected in ovarian and breast cancer cell lines, implicating the gene's potential role in the pathogenesis of human cancers. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":152321259,"end":152536101,"strand":-1,"description":"F-box and WD repeat domain containing 7 [Source:HGNC Symbol;Acc:HGNC:16712]"}, {"versioned_ensembl_gene_id":"ENSG00000243083.5","gene_symbol":"LINC00870","gene_name":"long intergenic non-protein coding RNA 870 [Source:HGNC Symbol;Acc:HGNC:27319]","synonyms":null,"biotype":"lincRNA","ncbi_id":"201617","summary":null,"start":72151257,"end":72174332,"strand":1,"description":"long intergenic non-protein coding RNA 870 [Source:HGNC Symbol;Acc:HGNC:27319]"}, {"versioned_ensembl_gene_id":"ENSG00000273461.5","gene_symbol":"AC105265.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72061061,"end":72069933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239350.2","gene_symbol":"AC105265.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72085109,"end":72085287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254880.1","gene_symbol":"PKNOX2-AS1","gene_name":"PKNOX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103695364","summary":null,"start":125158461,"end":125164609,"strand":-1,"description":"PKNOX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50690]"}, {"versioned_ensembl_gene_id":"ENSG00000249449.1","gene_symbol":"MRPL57P6","gene_name":"mitochondrial ribosomal protein L57 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29689]","synonyms":"MRP63P6","biotype":"processed_pseudogene","ncbi_id":"134490","summary":null,"start":163039291,"end":163039599,"strand":1,"description":"mitochondrial ribosomal protein L57 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29689]"}, {"versioned_ensembl_gene_id":"ENSG00000255433.5","gene_symbol":"AP001803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56848478,"end":56878078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283607.2","gene_symbol":"AC245166.3","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106354448,"end":106354704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231475.3","gene_symbol":"IGHV4-31","gene_name":"immunoglobulin heavy variable 4-31 [Source:HGNC Symbol;Acc:HGNC:5649]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28396","summary":null,"start":106349283,"end":106349792,"strand":-1,"description":"immunoglobulin heavy variable 4-31 [Source:HGNC Symbol;Acc:HGNC:5649]"}, {"versioned_ensembl_gene_id":"ENSG00000168944.15","gene_symbol":"CEP120","gene_name":"centrosomal protein 120 [Source:HGNC Symbol;Acc:HGNC:26690]","synonyms":"FLJ36090,CCDC100","biotype":"protein_coding","ncbi_id":"153241","summary":"This gene encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. A similar protein in mouse plays a role in both interkinetic nuclear migration, which is a characteristic pattern of nuclear movement in neural progenitors, and in neural progenitor self-renewal. Mutations in this gene are predicted to result in neurogenic defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":123344885,"end":123423592,"strand":-1,"description":"centrosomal protein 120 [Source:HGNC Symbol;Acc:HGNC:26690]"}, {"versioned_ensembl_gene_id":"ENSG00000148408.12","gene_symbol":"CACNA1B","gene_name":"calcium voltage-gated channel subunit alpha1 B [Source:HGNC Symbol;Acc:HGNC:1389]","synonyms":"Cav2.2,CACNN,CACNL1A5","biotype":"protein_coding","ncbi_id":"774","summary":"The protein encoded by this gene is the pore-forming subunit of an N-type voltage-dependent calcium channel, which controls neurotransmitter release from neurons. The encoded protein forms a complex with alpha-2, beta, and delta subunits to form the high-voltage activated channel. This channel is sensitive to omega-conotoxin-GVIA and omega-agatoxin-IIIA but insensitive to dihydropyridines. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":137877789,"end":138124624,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 B [Source:HGNC Symbol;Acc:HGNC:1389]"}, {"versioned_ensembl_gene_id":"ENSG00000275564.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54804243,"end":54821411,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000006062.14","gene_symbol":"MAP3K14","gene_name":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]","synonyms":"NIK,HSNIK,HS,FTDCR1B","biotype":"protein_coding","ncbi_id":"9020","summary":"This gene encodes mitogen-activated protein kinase kinase kinase 14, which is a serine/threonine protein-kinase. This kinase binds to TRAF2 and stimulates NF-kappaB activity. It shares sequence similarity with several other MAPKK kinases. It participates in an NF-kappaB-inducing signalling cascade common to receptors of the tumour-necrosis/nerve-growth factor (TNF/NGF) family and to the interleukin-1 type-I receptor. [provided by RefSeq, Jul 2008]","start":45263121,"end":45317040,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 14 [Source:HGNC Symbol;Acc:HGNC:6853]"}, {"versioned_ensembl_gene_id":"ENSG00000139835.13","gene_symbol":"GRTP1","gene_name":"growth hormone regulated TBC protein 1 [Source:HGNC Symbol;Acc:HGNC:20310]","synonyms":"TBC1D6,FLJ22474","biotype":"protein_coding","ncbi_id":"79774","summary":null,"start":113324164,"end":113364148,"strand":-1,"description":"growth hormone regulated TBC protein 1 [Source:HGNC Symbol;Acc:HGNC:20310]"}, {"versioned_ensembl_gene_id":"ENSG00000162849.15","gene_symbol":"KIF26B","gene_name":"kinesin family member 26B [Source:HGNC Symbol;Acc:HGNC:25484]","synonyms":"FLJ10157","biotype":"protein_coding","ncbi_id":"55083","summary":"The protein encoded by this gene is an intracellular motor protein thought to transport organelles along microtubules. The encoded protein is required for kidney development. Elevated levels of this protein have been found in some breast and colorectal cancers. [provided by RefSeq, Mar 2017]","start":245154985,"end":245709431,"strand":1,"description":"kinesin family member 26B [Source:HGNC Symbol;Acc:HGNC:25484]"}, {"versioned_ensembl_gene_id":"ENSG00000235706.7","gene_symbol":"DICER1-AS1","gene_name":"DICER1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43017]","synonyms":"FLJ45244,DICER1-AS","biotype":"antisense_RNA","ncbi_id":"400242","summary":null,"start":95157645,"end":95179933,"strand":1,"description":"DICER1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43017]"}, {"versioned_ensembl_gene_id":"ENSG00000270060.1","gene_symbol":"AC090589.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47168281,"end":47169563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282602.1","gene_symbol":"Z82244.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35372174,"end":35372621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250698.1","gene_symbol":"AC131182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140128015,"end":140134565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242083.2","gene_symbol":"AC068620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56356135,"end":56356932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224008.1","gene_symbol":"LINC01441","gene_name":"long intergenic non-protein coding RNA 1441 [Source:HGNC Symbol;Acc:HGNC:50763]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927796","summary":null,"start":55420336,"end":55427197,"strand":-1,"description":"long intergenic non-protein coding RNA 1441 [Source:HGNC Symbol;Acc:HGNC:50763]"}, {"versioned_ensembl_gene_id":"ENSG00000280148.1","gene_symbol":"AL049844.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":143857318,"end":143938471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271968.2","gene_symbol":"ADAM6","gene_name":"ADAM metallopeptidase domain 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:213]","synonyms":"tMDCIV,C14orf96","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"8755","summary":null,"start":105969729,"end":105972269,"strand":-1,"description":"ADAM metallopeptidase domain 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:213]"}, {"versioned_ensembl_gene_id":"ENSG00000196167.9","gene_symbol":"COLCA1","gene_name":"colorectal cancer associated 1 [Source:HGNC Symbol;Acc:HGNC:33789]","synonyms":"FLJ45803,CASC12,C11orf92","biotype":"antisense_RNA","ncbi_id":"399948","summary":"This gene encodes a transmembrane protein that localizes to granular structures, including crystalloid eosinophilic granules and other granular organelles. This gene, along with an overlapping opposite strand gene, has been implicated as a susceptibility locus for colorectal cancer. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":111290787,"end":111305045,"strand":-1,"description":"colorectal cancer associated 1 [Source:HGNC Symbol;Acc:HGNC:33789]"}, {"versioned_ensembl_gene_id":"ENSG00000118491.9","gene_symbol":"ZC2HC1B","gene_name":"zinc finger C2HC-type containing 1B [Source:HGNC Symbol;Acc:HGNC:21174]","synonyms":"FAM164B,dJ468K18.5,C6orf94","biotype":"protein_coding","ncbi_id":"153918","summary":null,"start":143864436,"end":143938356,"strand":1,"description":"zinc finger C2HC-type containing 1B [Source:HGNC Symbol;Acc:HGNC:21174]"}, {"versioned_ensembl_gene_id":"ENSG00000151655.18","gene_symbol":"ITIH2","gene_name":"inter-alpha-trypsin inhibitor heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:6167]","synonyms":"H2P","biotype":"protein_coding","ncbi_id":"3698","summary":"The inter-alpha-trypsin inhibitors (ITI) are a family of structurally related plasma serine protease inhibitors involved in extracellular matrix stabilization and in prevention of tumor metastasis. The ITI family contains multiple proteins made up of a light chain (see MIM 176870) and a variable number of heavy chains (Salier et al., 1987 [PubMed 2446322]; Himmelfarb et al., 2004 [PubMed 14744536]).[supplied by OMIM, Nov 2009]","start":7703269,"end":7749520,"strand":1,"description":"inter-alpha-trypsin inhibitor heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:6167]"}, {"versioned_ensembl_gene_id":"ENSG00000196646.11","gene_symbol":"ZNF136","gene_name":"zinc finger protein 136 [Source:HGNC Symbol;Acc:HGNC:12920]","synonyms":"pHZ-20","biotype":"protein_coding","ncbi_id":"7695","summary":"This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) A-box domain at its N-terminus, followed by fourteen contiguous C2H2 zinc finger domains and a degenerate zinc finger. The KRAB A-box showed weak transcriptional repressor activity in a reporter gene assay. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":12163064,"end":12189881,"strand":1,"description":"zinc finger protein 136 [Source:HGNC Symbol;Acc:HGNC:12920]"}, {"versioned_ensembl_gene_id":"ENSG00000172322.13","gene_symbol":"CLEC12A","gene_name":"C-type lectin domain family 12 member A [Source:HGNC Symbol;Acc:HGNC:31713]","synonyms":"MICL,DCAL-2,CLL-1,CD371","biotype":"protein_coding","ncbi_id":"160364","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The protein encoded by this gene is a negative regulator of granulocyte and monocyte function. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. This gene is closely linked to other CTL/CTLD superfamily members in the natural killer gene complex region on chromosome 12p13. [provided by RefSeq, May 2011]","start":9951316,"end":9995694,"strand":1,"description":"C-type lectin domain family 12 member A [Source:HGNC Symbol;Acc:HGNC:31713]"}, {"versioned_ensembl_gene_id":"ENSG00000256803.1","gene_symbol":"AC024224.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10015240,"end":10030606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223416.3","gene_symbol":"RPS26P15","gene_name":"ribosomal protein S26 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35680]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644928","summary":null,"start":58056133,"end":58056480,"strand":-1,"description":"ribosomal protein S26 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35680]"}, {"versioned_ensembl_gene_id":"ENSG00000230997.5","gene_symbol":"RAB42P1","gene_name":"RAB42, member RAS oncogene family, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19799]","synonyms":"RAB42,RAB42P","biotype":"processed_pseudogene","ncbi_id":"646996","summary":null,"start":89892128,"end":89892443,"strand":1,"description":"RAB42, member RAS oncogene family, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19799]"}, {"versioned_ensembl_gene_id":"ENSG00000258920.1","gene_symbol":"FOXN3-AS1","gene_name":"FOXN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44290]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"400236","summary":null,"start":89417354,"end":89419793,"strand":1,"description":"FOXN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44290]"}, {"versioned_ensembl_gene_id":"ENSG00000259050.2","gene_symbol":"CHORDC2P","gene_name":"cysteine and histidine rich domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:20050]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317775","summary":null,"start":89736965,"end":89738391,"strand":-1,"description":"cysteine and histidine rich domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:20050]"}, {"versioned_ensembl_gene_id":"ENSG00000227224.1","gene_symbol":"AC092035.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53474700,"end":53475089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172955.17","gene_symbol":"ADH6","gene_name":"alcohol dehydrogenase 6 (class V) [Source:HGNC Symbol;Acc:HGNC:255]","synonyms":"ADH-5","biotype":"protein_coding","ncbi_id":"130","summary":"This gene encodes class V alcohol dehydrogenase, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. This gene is expressed in the stomach as well as in the liver, and it contains a glucocorticoid response element upstream of its 5' UTR, which is a steroid hormone receptor binding site. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":99202638,"end":99219537,"strand":-1,"description":"alcohol dehydrogenase 6 (class V) [Source:HGNC Symbol;Acc:HGNC:255]"}, {"versioned_ensembl_gene_id":"ENSG00000226877.7","gene_symbol":"AL354733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83829656,"end":83837861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185046.18","gene_symbol":"ANKS1B","gene_name":"ankyrin repeat and sterile alpha motif domain containing 1B [Source:HGNC Symbol;Acc:HGNC:24600]","synonyms":"EB-1,cajalin-2,ANKS2,AIDA-1","biotype":"protein_coding","ncbi_id":"56899","summary":"This gene encodes a multi-domain protein that is predominantly expressed in brain and testis. This protein interacts with amyloid beta protein precursor (AbetaPP) and may have a role in normal brain development, and in the pathogenesis of Alzheimer's disease. Expression of this gene has been shown to be elevated in patients with pre-B cell acute lymphocytic leukemia associated with t(1;19) translocation. Alternatively spliced transcript variants encoding different isoforms (some with different subcellular localization, PMID:15004329) have been described for this gene. [provided by RefSeq, Aug 2011]","start":98726457,"end":99984654,"strand":-1,"description":"ankyrin repeat and sterile alpha motif domain containing 1B [Source:HGNC Symbol;Acc:HGNC:24600]"}, {"versioned_ensembl_gene_id":"ENSG00000220550.7","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439182,"end":29440853,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000224349.2","gene_symbol":"AL365226.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70412828,"end":70413950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211921.1","gene_symbol":"IGHD5-12","gene_name":"immunoglobulin heavy diversity 5-12 [Source:HGNC Symbol;Acc:HGNC:5508]","synonyms":"IGHD512,DK1","biotype":"IG_D_gene","ncbi_id":"28491","summary":null,"start":105902649,"end":105902671,"strand":-1,"description":"immunoglobulin heavy diversity 5-12 [Source:HGNC Symbol;Acc:HGNC:5508]"}, {"versioned_ensembl_gene_id":"ENSG00000237583.1","gene_symbol":"AC093166.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111675026,"end":111675343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211909.1","gene_symbol":"IGHD5-24","gene_name":"immunoglobulin heavy diversity 5-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5510]","synonyms":"IGHD524","biotype":"IG_D_gene","ncbi_id":"28489","summary":null,"start":105883903,"end":105883922,"strand":-1,"description":"immunoglobulin heavy diversity 5-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5510]"}, {"versioned_ensembl_gene_id":"ENSG00000131773.13","gene_symbol":"KHDRBS3","gene_name":"KH RNA binding domain containing, signal transduction associated 3 [Source:HGNC Symbol;Acc:HGNC:18117]","synonyms":"T-STAR,SLM2,SLM-2,SALP,etoile,Etle","biotype":"protein_coding","ncbi_id":"10656","summary":null,"start":135457457,"end":135656722,"strand":1,"description":"KH RNA binding domain containing, signal transduction associated 3 [Source:HGNC Symbol;Acc:HGNC:18117]"}, {"versioned_ensembl_gene_id":"ENSG00000270779.1","gene_symbol":"AC008782.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110908284,"end":110908713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232970.1","gene_symbol":"POLHP1","gene_name":"DNA polymerase eta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480782","summary":null,"start":216156342,"end":216156811,"strand":-1,"description":"DNA polymerase eta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43967]"}, {"versioned_ensembl_gene_id":"ENSG00000085231.13","gene_symbol":"AK6","gene_name":"adenylate kinase 6 [Source:HGNC Symbol;Acc:HGNC:49151]","synonyms":"CINAP","biotype":"protein_coding","ncbi_id":"102157402","summary":"This gene encodes a protein that belongs to the adenylate kinase family of enzymes. The protein has a nuclear localization and contains Walker A (P-loop) and Walker B motifs and a metal-coordinating residue. The protein may be involved in regulation of Cajal body formation. In human, AK6 and TAF9 (GeneID: 6880) are two distinct genes that share 5' exons. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":69350984,"end":69370013,"strand":-1,"description":"adenylate kinase 6 [Source:HGNC Symbol;Acc:HGNC:49151]"}, {"versioned_ensembl_gene_id":"ENSG00000253767.2","gene_symbol":"PCDHGA8","gene_name":"protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:HGNC:8706]","synonyms":"PCDH-GAMMA-A8,KIAA0327","biotype":"protein_coding","ncbi_id":"9708","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141390157,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:HGNC:8706]"}, {"versioned_ensembl_gene_id":"ENSG00000253873.5","gene_symbol":"PCDHGA11","gene_name":"protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:HGNC:8698]","synonyms":"PCDH-GAMMA-A11","biotype":"protein_coding","ncbi_id":"56105","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141421047,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:HGNC:8698]"}, {"versioned_ensembl_gene_id":"ENSG00000217268.1","gene_symbol":"TXNP7","gene_name":"thioredoxin pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480275","summary":null,"start":74004520,"end":74004812,"strand":-1,"description":"thioredoxin pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49487]"}, {"versioned_ensembl_gene_id":"ENSG00000116586.11","gene_symbol":"LAMTOR2","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 [Source:HGNC Symbol;Acc:HGNC:29796]","synonyms":"MAPKSP1AP,MAPBPIP,ENDAP,ROBLD3,Ragulator2,p14","biotype":"protein_coding","ncbi_id":"28956","summary":"The product of this gene is highly conserved with a mouse protein associated with the cytoplasmic face of late endosomes and lysosomes. The mouse protein interacts with MAPK scaffold protein 1, a component of the mitogen-activated protein kinase pathway. In humans, a mutation in this gene has been associated with a primary immunodeficiency syndrome, and suggests a role for this protein in endosomal biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":156054752,"end":156058510,"strand":1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 [Source:HGNC Symbol;Acc:HGNC:29796]"}, {"versioned_ensembl_gene_id":"ENSG00000160285.14","gene_symbol":"LSS","gene_name":"lanosterol synthase [Source:HGNC Symbol;Acc:HGNC:6708]","synonyms":"OSC","biotype":"protein_coding","ncbi_id":"4047","summary":"The protein encoded by this gene catalyzes the conversion of (S)-2,3 oxidosqualene to lanosterol. The encoded protein is a member of the terpene cyclase/mutase family and catalyzes the first step in the biosynthesis of cholesterol, steroid hormones, and vitamin D. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2009]","start":46188141,"end":46228824,"strand":-1,"description":"lanosterol synthase [Source:HGNC Symbol;Acc:HGNC:6708]"}, {"versioned_ensembl_gene_id":"ENSG00000205517.12","gene_symbol":"RGL3","gene_name":"ral guanine nucleotide dissociation stimulator like 3 [Source:HGNC Symbol;Acc:HGNC:30282]","synonyms":"FLJ32585","biotype":"protein_coding","ncbi_id":"57139","summary":null,"start":11384341,"end":11419342,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 3 [Source:HGNC Symbol;Acc:HGNC:30282]"}, {"versioned_ensembl_gene_id":"ENSG00000255500.2","gene_symbol":"AC109635.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50268161,"end":50269273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115392.11","gene_symbol":"FANCL","gene_name":"Fanconi anemia complementation group L [Source:HGNC Symbol;Acc:HGNC:20748]","synonyms":"Pog,PHF9,FLJ10335,FAAP43","biotype":"protein_coding","ncbi_id":"55120","summary":"This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018]","start":58159243,"end":58241372,"strand":-1,"description":"Fanconi anemia complementation group L [Source:HGNC Symbol;Acc:HGNC:20748]"}, {"versioned_ensembl_gene_id":"ENSG00000175820.3","gene_symbol":"CCDC168","gene_name":"coiled-coil domain containing 168 [Source:HGNC Symbol;Acc:HGNC:26851]","synonyms":"FLJ40176,C13orf40","biotype":"protein_coding","ncbi_id":"643677","summary":null,"start":102729369,"end":102759070,"strand":-1,"description":"coiled-coil domain containing 168 [Source:HGNC Symbol;Acc:HGNC:26851]"}, {"versioned_ensembl_gene_id":"ENSG00000231633.1","gene_symbol":"LINC00283","gene_name":"long intergenic non-protein coding RNA 283 [Source:HGNC Symbol;Acc:HGNC:38809]","synonyms":"NCRNA00283","biotype":"antisense_RNA","ncbi_id":"100874057","summary":null,"start":102742990,"end":102745224,"strand":1,"description":"long intergenic non-protein coding RNA 283 [Source:HGNC Symbol;Acc:HGNC:38809]"}, {"versioned_ensembl_gene_id":"ENSG00000139436.20","gene_symbol":"GIT2","gene_name":"GIT ArfGAP 2 [Source:HGNC Symbol;Acc:HGNC:4273]","synonyms":"PKL,KIAA0148","biotype":"protein_coding","ncbi_id":"9815","summary":"This gene encodes a member of the GIT protein family, which interact with G protein-coupled receptor kinases and possess ADP-ribosylation factor (ARF) GTPase-activating protein (GAP) activity. GIT proteins traffic between cytoplasmic complexes, focal adhesions, and the cell periphery, and interact with Pak interacting exchange factor beta (PIX) to form large oligomeric complexes that transiently recruit other proteins. GIT proteins regulate cytoskeletal dynamics and participate in receptor internalization and membrane trafficking. This gene has been shown to repress lamellipodial extension and focal adhesion turnover, and is thought to regulate cell motility. This gene undergoes extensive alternative splicing to generate multiple isoforms, but the full-length nature of some of these variants has not been determined. The various isoforms have functional differences, with respect to ARF GAP activity and to G protein-coupled receptor kinase 2 binding. [provided by RefSeq, Sep 2008]","start":109929792,"end":109996389,"strand":-1,"description":"GIT ArfGAP 2 [Source:HGNC Symbol;Acc:HGNC:4273]"}, {"versioned_ensembl_gene_id":"ENSG00000247317.3","gene_symbol":"AC105202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142981738,"end":143018437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154803.12","gene_symbol":"FLCN","gene_name":"folliculin [Source:HGNC Symbol;Acc:HGNC:27310]","synonyms":"MGC17998,BHD,MGC23445","biotype":"protein_coding","ncbi_id":"201163","summary":"This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":17212212,"end":17237188,"strand":-1,"description":"folliculin [Source:HGNC Symbol;Acc:HGNC:27310]"}, {"versioned_ensembl_gene_id":"ENSG00000134452.19","gene_symbol":"FBXO18","gene_name":"F-box protein, helicase, 18 [Source:HGNC Symbol;Acc:HGNC:13620]","synonyms":"FLJ14590,Fbx18,FBH1","biotype":"protein_coding","ncbi_id":"84893","summary":"This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into three classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbx class. It contains an F-box motif and seven conserved helicase motifs, and has both DNA-dependent ATPase and DNA unwinding activities. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":5890203,"end":5937594,"strand":1,"description":"F-box protein, helicase, 18 [Source:HGNC Symbol;Acc:HGNC:13620]"}, {"versioned_ensembl_gene_id":"ENSG00000153922.10","gene_symbol":"CHD1","gene_name":"chromodomain helicase DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1915]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1105","summary":"The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. [provided by RefSeq, Jul 2008]","start":98853985,"end":98928957,"strand":-1,"description":"chromodomain helicase DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1915]"}, {"versioned_ensembl_gene_id":"ENSG00000278664.1","gene_symbol":"DUX4L10","gene_name":"double homeobox 4 like 10 [Source:HGNC Symbol;Acc:HGNC:31354]","synonyms":"DUX10","biotype":"unprocessed_pseudogene","ncbi_id":"440013","summary":null,"start":133743332,"end":133744598,"strand":1,"description":"double homeobox 4 like 10 [Source:HGNC Symbol;Acc:HGNC:31354]"}, {"versioned_ensembl_gene_id":"ENSG00000234112.2","gene_symbol":"AC099066.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":225803148,"end":225803448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256896.1","gene_symbol":"PSMC1P8","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390297","summary":null,"start":17383352,"end":17384647,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39783]"}, {"versioned_ensembl_gene_id":"ENSG00000086475.14","gene_symbol":"SEPHS1","gene_name":"selenophosphate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:19685]","synonyms":"SPS1,SPS","biotype":"protein_coding","ncbi_id":"22929","summary":"This gene encodes an enzyme that synthesizes selenophosphate from selenide and ATP. Selenophosphate is the selenium donor used to synthesize selenocysteine, which is co-translationally incorporated into selenoproteins at in-frame UGA codons. [provided by RefSeq, Sep 2010]","start":13317424,"end":13348298,"strand":-1,"description":"selenophosphate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:19685]"}, {"versioned_ensembl_gene_id":"ENSG00000259006.1","gene_symbol":"AC092143.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89919827,"end":89922662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123297.17","gene_symbol":"TSFM","gene_name":"Ts translation elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12367]","synonyms":"EF-Tsmt,EF-TS","biotype":"protein_coding","ncbi_id":"10102","summary":"This gene encodes a mitochondrial translation elongation factor. The encoded protein is an enzyme that catalyzes the exchange of guanine nucleotides on the translation elongation factor Tu during the elongation step of mitchondrial protein translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-3 syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]","start":57782589,"end":57808071,"strand":1,"description":"Ts translation elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12367]"}, {"versioned_ensembl_gene_id":"ENSG00000041802.10","gene_symbol":"LSG1","gene_name":"large 60S subunit nuclear export GTPase 1 [Source:HGNC Symbol;Acc:HGNC:25652]","synonyms":"FLJ11301","biotype":"protein_coding","ncbi_id":"55341","summary":"This gene encodes a protein related to the yeast large subunit GTPase 1. The encoded protein is necessary for cell viability and may localize in the endoplasmic reticulum, nucleus and cytoplasm.[provided by RefSeq, Feb 2009]","start":194640788,"end":194672477,"strand":-1,"description":"large 60S subunit nuclear export GTPase 1 [Source:HGNC Symbol;Acc:HGNC:25652]"}, {"versioned_ensembl_gene_id":"ENSG00000275654.1","gene_symbol":"AC138894.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28451644,"end":28455356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282002.1","gene_symbol":"AC243807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45561416,"end":45570373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258251.1","gene_symbol":"YPEL5P3","gene_name":"YPEL5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100653396","summary":null,"start":96060024,"end":96060375,"strand":-1,"description":"YPEL5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50557]"}, {"versioned_ensembl_gene_id":"ENSG00000145839.1","gene_symbol":"IL9","gene_name":"interleukin 9 [Source:HGNC Symbol;Acc:HGNC:6029]","synonyms":"P40,IL-9,HP40","biotype":"protein_coding","ncbi_id":"3578","summary":"The protein encoded by this gene is a cytokine that acts as a regulator of a variety of hematopoietic cells. This cytokine stimulates cell proliferation and prevents apoptosis. It functions through the interleukin 9 receptor (IL9R), which activates different signal transducer and activator (STAT) proteins and thus connects this cytokine to various biological processes. The gene encoding this cytokine has been identified as a candidate gene for asthma. Genetic studies on a mouse model of asthma demonstrated that this cytokine is a determining factor in the pathogenesis of bronchial hyperresponsiveness. [provided by RefSeq, Jul 2008]","start":135892246,"end":135895827,"strand":-1,"description":"interleukin 9 [Source:HGNC Symbol;Acc:HGNC:6029]"}, {"versioned_ensembl_gene_id":"ENSG00000267044.1","gene_symbol":"AC005757.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45135993,"end":45136977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267346.1","gene_symbol":"EIF5AP3","gene_name":"eukaryotic translation initiation factor 5A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3304]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1987","summary":null,"start":45128569,"end":45129030,"strand":1,"description":"eukaryotic translation initiation factor 5A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3304]"}, {"versioned_ensembl_gene_id":"ENSG00000255435.6","gene_symbol":"AP001267.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118511911,"end":118531094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181826.9","gene_symbol":"RELL1","gene_name":"RELT like 1 [Source:HGNC Symbol;Acc:HGNC:27379]","synonyms":null,"biotype":"protein_coding","ncbi_id":"768211","summary":null,"start":37590800,"end":37686376,"strand":-1,"description":"RELT like 1 [Source:HGNC Symbol;Acc:HGNC:27379]"}, {"versioned_ensembl_gene_id":"ENSG00000254983.1","gene_symbol":"AC025300.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12303533,"end":12308216,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103423.13","gene_symbol":"DNAJA3","gene_name":"DnaJ heat shock protein family (Hsp40) member A3 [Source:HGNC Symbol;Acc:HGNC:11808]","synonyms":"TID1,hTid-1","biotype":"protein_coding","ncbi_id":"9093","summary":"This gene encodes a member of the DNAJ/Hsp40 protein family. DNAJ/Hsp40 proteins stimulate the ATPase activity of Hsp70 chaperones and play critical roles in protein folding, degradation, and multimeric complex assembly. The encoded protein is localized to mitochondria and mediates several cellular processes including proliferation, survival and apoptotic signal transduction. The encoded protein also plays a critical role in tumor suppression through interactions with oncogenic proteins including ErbB2 and the p53 tumor suppressor protein. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":4425805,"end":4456775,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A3 [Source:HGNC Symbol;Acc:HGNC:11808]"}, {"versioned_ensembl_gene_id":"ENSG00000283662.1","gene_symbol":"AC138904.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28258686,"end":28292173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228040.1","gene_symbol":"AL390729.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112890767,"end":112890922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133895.14","gene_symbol":"MEN1","gene_name":"menin 1 [Source:HGNC Symbol;Acc:HGNC:7010]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4221","summary":"This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic gene regulation. It is thought to regulate several pathways and processes by altering chromatin structure through the modification of histones. [provided by RefSeq, May 2019]","start":64803510,"end":64811294,"strand":-1,"description":"menin 1 [Source:HGNC Symbol;Acc:HGNC:7010]"}, {"versioned_ensembl_gene_id":"ENSG00000163519.13","gene_symbol":"TRAT1","gene_name":"T-cell receptor associated transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:30698]","synonyms":"TRIM,TCRIM,HSPC062","biotype":"protein_coding","ncbi_id":"50852","summary":null,"start":108822698,"end":108855005,"strand":1,"description":"T-cell receptor associated transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:30698]"}, {"versioned_ensembl_gene_id":"ENSG00000260477.7","gene_symbol":"LINC01584","gene_name":"long intergenic non-protein coding RNA 1584 [Source:HGNC Symbol;Acc:HGNC:51426]","synonyms":"TCONS_00024001","biotype":"antisense_RNA","ncbi_id":"101929701","summary":null,"start":86078809,"end":86116717,"strand":-1,"description":"long intergenic non-protein coding RNA 1584 [Source:HGNC Symbol;Acc:HGNC:51426]"}, {"versioned_ensembl_gene_id":"ENSG00000165389.6","gene_symbol":"SPTSSA","gene_name":"serine palmitoyltransferase small subunit A [Source:HGNC Symbol;Acc:HGNC:20361]","synonyms":"ssSPTa,C14orf147","biotype":"protein_coding","ncbi_id":"171546","summary":"Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTA is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010]","start":34432789,"end":34462356,"strand":-1,"description":"serine palmitoyltransferase small subunit A [Source:HGNC Symbol;Acc:HGNC:20361]"}, {"versioned_ensembl_gene_id":"ENSG00000260125.1","gene_symbol":"AGBL1-AS1","gene_name":"AGBL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48617]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"727915","summary":null,"start":86295649,"end":86317173,"strand":-1,"description":"AGBL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48617]"}, {"versioned_ensembl_gene_id":"ENSG00000259608.1","gene_symbol":"AC104229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85958717,"end":85958971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083838.15","gene_symbol":"ZNF446","gene_name":"zinc finger protein 446 [Source:HGNC Symbol;Acc:HGNC:21036]","synonyms":"ZSCAN52,ZKSCAN20,FLJ20626","biotype":"protein_coding","ncbi_id":"55663","summary":null,"start":58474017,"end":58481230,"strand":1,"description":"zinc finger protein 446 [Source:HGNC Symbol;Acc:HGNC:21036]"}, {"versioned_ensembl_gene_id":"ENSG00000255526.6","gene_symbol":"NEDD8-MDP1","gene_name":"NEDD8-MDP1 readthrough [Source:HGNC Symbol;Acc:HGNC:39551]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528064","summary":"This locus represents naturally occurring read-through transcription between the neighboring NEDD8 (neural precursor cell expressed, developmentally down-regulated 8) and MDP1 (magnesium-dependent phosphatase 1) genes on chromosome 14. One of the read-through transcripts on this locus encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Jul 2016]","start":24213955,"end":24232352,"strand":-1,"description":"NEDD8-MDP1 readthrough [Source:HGNC Symbol;Acc:HGNC:39551]"}, {"versioned_ensembl_gene_id":"ENSG00000176134.5","gene_symbol":"AL445665.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64637845,"end":64652556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239706.1","gene_symbol":"AC117392.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156988117,"end":156988712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213016.3","gene_symbol":"AC245036.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54521723,"end":54522031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253415.1","gene_symbol":"AC016877.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98904603,"end":98905671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255871.2","gene_symbol":"AC007529.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16693800,"end":16695977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260276.2","gene_symbol":"AC022167.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8848105,"end":8860456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233762.3","gene_symbol":"AC007969.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171517270,"end":171517716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154222.14","gene_symbol":"CC2D1B","gene_name":"coiled-coil and C2 domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29386]","synonyms":"KIAA1836","biotype":"protein_coding","ncbi_id":"200014","summary":null,"start":52345723,"end":52366193,"strand":-1,"description":"coiled-coil and C2 domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29386]"}, {"versioned_ensembl_gene_id":"ENSG00000267678.1","gene_symbol":"AC011921.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60562010,"end":60562161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253725.1","gene_symbol":"AC126915.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178840097,"end":178841134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249152.1","gene_symbol":"LNCPRESS2","gene_name":"lncRNA p53 regulated and ESC associated 2 [Source:HGNC Symbol;Acc:HGNC:52747]","synonyms":"lncPRESS2","biotype":"lincRNA","ncbi_id":"101929194","summary":null,"start":92268767,"end":92277075,"strand":-1,"description":"lncRNA p53 regulated and ESC associated 2 [Source:HGNC Symbol;Acc:HGNC:52747]"}, {"versioned_ensembl_gene_id":"ENSG00000189377.8","gene_symbol":"CXCL17","gene_name":"C-X-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:19232]","synonyms":"VCC1,UNQ473,DMC,Dcip1","biotype":"protein_coding","ncbi_id":"284340","summary":"The protein encoded by this gene is a mucosal chemokine that attracts immature dendritic cells and blood monocytes to the lungs. The encoded protein also promotes tumorigenesis through an angiogenic activity. Finally, this protein exhibits strong antimicrobial activity against E. coli, S. aureus, Salmonella, P. aeruginosa, and C. albicans. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":42428288,"end":42443048,"strand":-1,"description":"C-X-C motif chemokine ligand 17 [Source:HGNC Symbol;Acc:HGNC:19232]"}, {"versioned_ensembl_gene_id":"ENSG00000254942.1","gene_symbol":"AL355310.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109539906,"end":109543837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106686.16","gene_symbol":"SPATA6L","gene_name":"spermatogenesis associated 6 like [Source:HGNC Symbol;Acc:HGNC:25472]","synonyms":"FLJ10058,C9orf68","biotype":"protein_coding","ncbi_id":"55064","summary":null,"start":4553386,"end":4666674,"strand":-1,"description":"spermatogenesis associated 6 like [Source:HGNC Symbol;Acc:HGNC:25472]"}, {"versioned_ensembl_gene_id":"ENSG00000260328.1","gene_symbol":"AC104024.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17011914,"end":17014990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168010.10","gene_symbol":"ATG16L2","gene_name":"autophagy related 16 like 2 [Source:HGNC Symbol;Acc:HGNC:25464]","synonyms":"WDR80,FLJ00012,ATG16B","biotype":"protein_coding","ncbi_id":"89849","summary":null,"start":72814308,"end":72843674,"strand":1,"description":"autophagy related 16 like 2 [Source:HGNC Symbol;Acc:HGNC:25464]"}, {"versioned_ensembl_gene_id":"ENSG00000260450.1","gene_symbol":"LINC02134","gene_name":"long intergenic non-protein coding RNA 2134 [Source:HGNC Symbol;Acc:HGNC:52994]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371238","summary":null,"start":47965672,"end":47971687,"strand":1,"description":"long intergenic non-protein coding RNA 2134 [Source:HGNC Symbol;Acc:HGNC:52994]"}, {"versioned_ensembl_gene_id":"ENSG00000263252.1","gene_symbol":"AC005341.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53353427,"end":53354134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128298.16","gene_symbol":"BAIAP2L2","gene_name":"BAI1 associated protein 2 like 2 [Source:HGNC Symbol;Acc:HGNC:26203]","synonyms":"pinkbar,FLJ22582","biotype":"protein_coding","ncbi_id":"80115","summary":"The protein encoded by this gene binds phosphoinositides and promotes the formation of planar or curved membrane structures. The encoded protein is found in RAB13-positive vesicles and at intercellular contacts with the plasma membrane. [provided by RefSeq, Dec 2012]","start":38084889,"end":38110670,"strand":-1,"description":"BAI1 associated protein 2 like 2 [Source:HGNC Symbol;Acc:HGNC:26203]"}, {"versioned_ensembl_gene_id":"ENSG00000237750.2","gene_symbol":"AC011900.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162768936,"end":162797972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235233.9","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31442784,"end":31459233,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000213270.5","gene_symbol":"AC090680.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83151331,"end":83152190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276789.1","gene_symbol":"AC103974.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18836304,"end":18837081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225411.2","gene_symbol":"CR786580.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63802144,"end":63814159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248998.2","gene_symbol":"EFTUD1P2","gene_name":"elongation factor Tu GTP binding domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44202]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422019","summary":null,"start":65142703,"end":65145763,"strand":-1,"description":"elongation factor Tu GTP binding domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44202]"}, {"versioned_ensembl_gene_id":"ENSG00000251193.1","gene_symbol":"AC112203.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97737894,"end":97738913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248447.2","gene_symbol":"AC107058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65034634,"end":65036017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074803.17","gene_symbol":"SLC12A1","gene_name":"solute carrier family 12 member 1 [Source:HGNC Symbol;Acc:HGNC:10910]","synonyms":"NKCC2","biotype":"protein_coding","ncbi_id":"6557","summary":"This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa. It plays a key role in concentrating urine and accounts for most of the NaCl resorption. It is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity in humans has not been experimentally proven.[provided by RefSeq, May 2010]","start":48191664,"end":48304078,"strand":1,"description":"solute carrier family 12 member 1 [Source:HGNC Symbol;Acc:HGNC:10910]"}, {"versioned_ensembl_gene_id":"ENSG00000205710.3","gene_symbol":"C17orf107","gene_name":"chromosome 17 open reading frame 107 [Source:HGNC Symbol;Acc:HGNC:37238]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130311","summary":null,"start":4899418,"end":4902932,"strand":1,"description":"chromosome 17 open reading frame 107 [Source:HGNC Symbol;Acc:HGNC:37238]"}, {"versioned_ensembl_gene_id":"ENSG00000233932.4","gene_symbol":"CTXN2","gene_name":"cortexin 2 [Source:HGNC Symbol;Acc:HGNC:31109]","synonyms":null,"biotype":"protein_coding","ncbi_id":"399697","summary":null,"start":48191539,"end":48203756,"strand":1,"description":"cortexin 2 [Source:HGNC Symbol;Acc:HGNC:31109]"}, {"versioned_ensembl_gene_id":"ENSG00000213108.3","gene_symbol":"BTF3L4P3","gene_name":"basic transcription factor 3 like 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391040","summary":null,"start":137543897,"end":137544372,"strand":-1,"description":"basic transcription factor 3 like 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39647]"}, {"versioned_ensembl_gene_id":"ENSG00000165322.17","gene_symbol":"ARHGAP12","gene_name":"Rho GTPase activating protein 12 [Source:HGNC Symbol;Acc:HGNC:16348]","synonyms":"FLJ21785,FLJ20737,FLJ10971","biotype":"protein_coding","ncbi_id":"94134","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may be involved in suppressing tumor formation by regulating cell invasion and adhesion. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31805404,"end":31928876,"strand":-1,"description":"Rho GTPase activating protein 12 [Source:HGNC Symbol;Acc:HGNC:16348]"}, {"versioned_ensembl_gene_id":"ENSG00000276431.1","gene_symbol":"AC023511.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30169881,"end":30170091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130193.7","gene_symbol":"THEM6","gene_name":"thioesterase superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:29656]","synonyms":"DSCD75,C8orf55","biotype":"protein_coding","ncbi_id":"51337","summary":null,"start":142727203,"end":142736927,"strand":1,"description":"thioesterase superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:29656]"}, {"versioned_ensembl_gene_id":"ENSG00000153721.18","gene_symbol":"CNKSR3","gene_name":"CNKSR family member 3 [Source:HGNC Symbol;Acc:HGNC:23034]","synonyms":"MAGI1,FLJ31349","biotype":"protein_coding","ncbi_id":"154043","summary":null,"start":154387504,"end":154510659,"strand":-1,"description":"CNKSR family member 3 [Source:HGNC Symbol;Acc:HGNC:23034]"}, {"versioned_ensembl_gene_id":"ENSG00000254349.5","gene_symbol":"MIR2052HG","gene_name":"MIR2052 host gene [Source:HGNC Symbol;Acc:HGNC:51555]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441355","summary":null,"start":74599775,"end":74823313,"strand":1,"description":"MIR2052 host gene [Source:HGNC Symbol;Acc:HGNC:51555]"}, {"versioned_ensembl_gene_id":"ENSG00000229515.1","gene_symbol":"FLT1P1","gene_name":"fms related tyrosine kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44609]","synonyms":"LOC391533","biotype":"processed_pseudogene","ncbi_id":"391533","summary":null,"start":46142358,"end":46143677,"strand":-1,"description":"fms related tyrosine kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44609]"}, {"versioned_ensembl_gene_id":"ENSG00000140961.12","gene_symbol":"OSGIN1","gene_name":"oxidative stress induced growth inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:30093]","synonyms":"OKL38,BDGI","biotype":"protein_coding","ncbi_id":"29948","summary":"This gene encodes an oxidative stress response protein that regulates cell death. Expression of the gene is regulated by p53 and is induced by DNA damage. The protein regulates apoptosis by inducing cytochrome c release from mitochondria. It also appears to be a key regulator of both inflammatory and anti-inflammatory molecules. The loss of this protein correlates with uncontrolled cell growth and tumor formation. Naturally occurring read-through transcription exists between this gene and the neighboring upstream malonyl-CoA decarboxylase (MLYCD) gene, but the read-through transcripts are unlikely to produce a protein product. [provided by RefSeq, Aug 2011]","start":83948282,"end":83966332,"strand":1,"description":"oxidative stress induced growth inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:30093]"}, {"versioned_ensembl_gene_id":"ENSG00000271589.1","gene_symbol":"AL139395.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74769639,"end":74769798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162881.6","gene_symbol":"OXER1","gene_name":"oxoeicosanoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:24884]","synonyms":"GPCR,TG1019,GPR170","biotype":"protein_coding","ncbi_id":"165140","summary":null,"start":42762481,"end":42764261,"strand":-1,"description":"oxoeicosanoid receptor 1 [Source:HGNC Symbol;Acc:HGNC:24884]"}, {"versioned_ensembl_gene_id":"ENSG00000162804.13","gene_symbol":"SNED1","gene_name":"sushi, nidogen and EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:24696]","synonyms":"SST3,Snep,FLJ00133","biotype":"protein_coding","ncbi_id":"25992","summary":null,"start":240998838,"end":241095568,"strand":1,"description":"sushi, nidogen and EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:24696]"}, {"versioned_ensembl_gene_id":"ENSG00000225265.1","gene_symbol":"TAF1A-AS1","gene_name":"TAF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40573]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506161","summary":null,"start":222589825,"end":222593032,"strand":1,"description":"TAF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40573]"}, {"versioned_ensembl_gene_id":"ENSG00000224594.2","gene_symbol":"AC041040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48384590,"end":48385049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253843.1","gene_symbol":"AC104989.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48193850,"end":48194627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251298.1","gene_symbol":"AC093835.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147609552,"end":147617245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175309.14","gene_symbol":"PHYKPL","gene_name":"5-phosphohydroxy-L-lysine phospho-lyase [Source:HGNC Symbol;Acc:HGNC:28249]","synonyms":"MGC15875,AGXT2L2","biotype":"protein_coding","ncbi_id":"85007","summary":"This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":178208497,"end":178232791,"strand":-1,"description":"5-phosphohydroxy-L-lysine phospho-lyase [Source:HGNC Symbol;Acc:HGNC:28249]"}, {"versioned_ensembl_gene_id":"ENSG00000011260.13","gene_symbol":"UTP18","gene_name":"UTP18, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24274]","synonyms":"WDR50,CGI-48","biotype":"protein_coding","ncbi_id":"51096","summary":null,"start":51260528,"end":51297936,"strand":1,"description":"UTP18, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24274]"}, {"versioned_ensembl_gene_id":"ENSG00000269243.1","gene_symbol":"AC008894.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16123661,"end":16139892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145916.18","gene_symbol":"RMND5B","gene_name":"required for meiotic nuclear division 5 homolog B [Source:HGNC Symbol;Acc:HGNC:26181]","synonyms":"GID2B,GID2,FLJ22318","biotype":"protein_coding","ncbi_id":"64777","summary":null,"start":178130996,"end":178150565,"strand":1,"description":"required for meiotic nuclear division 5 homolog B [Source:HGNC Symbol;Acc:HGNC:26181]"}, {"versioned_ensembl_gene_id":"ENSG00000113734.17","gene_symbol":"BNIP1","gene_name":"BCL2 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:1082]","synonyms":"Nip1,SEC20","biotype":"protein_coding","ncbi_id":"662","summary":"This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. In addition, this protein is involved in vesicle transport into the endoplasmic reticulum. Alternative splicing of this gene results in four protein products with identical N- and C-termini. [provided by RefSeq, Mar 2011]","start":173144442,"end":173164387,"strand":1,"description":"BCL2 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:1082]"}, {"versioned_ensembl_gene_id":"ENSG00000253172.1","gene_symbol":"AC008378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173144162,"end":173145039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280839.2","gene_symbol":"CES5AP1","gene_name":"carboxylesterase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38516]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"649264","summary":null,"start":23359603,"end":23387731,"strand":-1,"description":"carboxylesterase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38516]"}, {"versioned_ensembl_gene_id":"ENSG00000164674.15","gene_symbol":"SYTL3","gene_name":"synaptotagmin like 3 [Source:HGNC Symbol;Acc:HGNC:15587]","synonyms":"SLP3,exophilin-6","biotype":"protein_coding","ncbi_id":"94120","summary":"The protein encoded by this gene belongs to a family of peripheral membrane proteins that play a role in vesicular trafficking. This protein binds phospholipids in the presence of calcium ions. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":158650014,"end":158764876,"strand":1,"description":"synaptotagmin like 3 [Source:HGNC Symbol;Acc:HGNC:15587]"}, {"versioned_ensembl_gene_id":"ENSG00000257837.1","gene_symbol":"AC089998.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82505211,"end":82506188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267318.1","gene_symbol":"AC005702.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":59940908,"end":59973101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224751.2","gene_symbol":"SHMT1P1","gene_name":"serine hydroxymethyltransferase 1 (soluble) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10851]","synonyms":"SHMT1P","biotype":"processed_pseudogene","ncbi_id":"6471","summary":null,"start":43850300,"end":43851611,"strand":-1,"description":"serine hydroxymethyltransferase 1 (soluble) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10851]"}, {"versioned_ensembl_gene_id":"ENSG00000236200.5","gene_symbol":"KDM4A-AS1","gene_name":"KDM4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40528]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132774","summary":null,"start":43699765,"end":43708138,"strand":-1,"description":"KDM4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40528]"}, {"versioned_ensembl_gene_id":"ENSG00000272941.1","gene_symbol":"AC083862.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135168403,"end":135169547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237123.2","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31108861,"end":31114200,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000236760.1","gene_symbol":"AC019118.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3131581,"end":3145780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275501.4","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195720882,"end":195741123,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000260761.1","gene_symbol":"AC106754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25319834,"end":25321346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157965.11","gene_symbol":"SSX8","gene_name":"SSX family member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:19654]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"280659","summary":null,"start":52624998,"end":52632895,"strand":1,"description":"SSX family member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:19654]"}, {"versioned_ensembl_gene_id":"ENSG00000176495.3","gene_symbol":"OR5AN1","gene_name":"olfactory receptor family 5 subfamily AN member 1 [Source:HGNC Symbol;Acc:HGNC:15255]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390195","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59358895,"end":59371714,"strand":1,"description":"olfactory receptor family 5 subfamily AN member 1 [Source:HGNC Symbol;Acc:HGNC:15255]"}, {"versioned_ensembl_gene_id":"ENSG00000167751.12","gene_symbol":"KLK2","gene_name":"kallikrein related peptidase 2 [Source:HGNC Symbol;Acc:HGNC:6363]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3817","summary":"This gene encodes a member of the grandular kallikrein protein family. Kallikreins are a subgroup of serine proteases that are clustered on chromosome 19. Members of this family are involved in a diverse array of biological functions. The protein encoded by this gene is a highly active trypsin-like serine protease that selectively cleaves at arginine residues. This protein is primarily expressed in prostatic tissue and is responsible for cleaving pro-prostate-specific antigen into its enzymatically active form. This gene is highly expressed in prostate tumor cells and may be a prognostic maker for prostate cancer risk. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Jan 2012]","start":50861568,"end":50880567,"strand":1,"description":"kallikrein related peptidase 2 [Source:HGNC Symbol;Acc:HGNC:6363]"}, {"versioned_ensembl_gene_id":"ENSG00000218226.1","gene_symbol":"TATDN2P2","gene_name":"TatD DNase domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39255]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100272205","summary":null,"start":158609706,"end":158621636,"strand":-1,"description":"TatD DNase domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39255]"}, {"versioned_ensembl_gene_id":"ENSG00000204991.10","gene_symbol":"SPIRE2","gene_name":"spire type actin nucleation factor 2 [Source:HGNC Symbol;Acc:HGNC:30623]","synonyms":"spir-2,KIAA1832","biotype":"protein_coding","ncbi_id":"84501","summary":null,"start":89818179,"end":89871319,"strand":1,"description":"spire type actin nucleation factor 2 [Source:HGNC Symbol;Acc:HGNC:30623]"}, {"versioned_ensembl_gene_id":"ENSG00000234520.5","gene_symbol":"HRAT17","gene_name":"heart tissue-associated transcript 17 [Source:NCBI gene;Acc:101928036]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928036","summary":null,"start":112954646,"end":112995634,"strand":-1,"description":"heart tissue-associated transcript 17 [Source:NCBI gene;Acc:101928036]"}, {"versioned_ensembl_gene_id":"ENSG00000102466.15","gene_symbol":"FGF14","gene_name":"fibroblast growth factor 14 [Source:HGNC Symbol;Acc:HGNC:3671]","synonyms":"SCA27,FHF4","biotype":"protein_coding","ncbi_id":"2259","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":101710804,"end":102402457,"strand":-1,"description":"fibroblast growth factor 14 [Source:HGNC Symbol;Acc:HGNC:3671]"}, {"versioned_ensembl_gene_id":"ENSG00000249129.1","gene_symbol":"SUDS3P1","gene_name":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285647","summary":null,"start":177971316,"end":177972281,"strand":1,"description":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]"}, {"versioned_ensembl_gene_id":"ENSG00000265408.1","gene_symbol":"AC009084.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":66942712,"end":66963256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243995.3","gene_symbol":"AL035660.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45230868,"end":45233331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104853.15","gene_symbol":"CLPTM1","gene_name":"CLPTM1, transmembrane protein [Source:HGNC Symbol;Acc:HGNC:2087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1209","summary":null,"start":44954585,"end":44993341,"strand":1,"description":"CLPTM1, transmembrane protein [Source:HGNC Symbol;Acc:HGNC:2087]"}, {"versioned_ensembl_gene_id":"ENSG00000268866.1","gene_symbol":"AC020915.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58224506,"end":58225469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102119.10","gene_symbol":"EMD","gene_name":"emerin [Source:HGNC Symbol;Acc:HGNC:3331]","synonyms":"LEMD5,STA","biotype":"protein_coding","ncbi_id":"2010","summary":"Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene. [provided by RefSeq, Jul 2008]","start":154379197,"end":154381523,"strand":1,"description":"emerin [Source:HGNC Symbol;Acc:HGNC:3331]"}, {"versioned_ensembl_gene_id":"ENSG00000186075.12","gene_symbol":"ZPBP2","gene_name":"zona pellucida binding protein 2 [Source:HGNC Symbol;Acc:HGNC:20678]","synonyms":"ZPBPL,MGC41930","biotype":"protein_coding","ncbi_id":"124626","summary":null,"start":39868164,"end":39877896,"strand":1,"description":"zona pellucida binding protein 2 [Source:HGNC Symbol;Acc:HGNC:20678]"}, {"versioned_ensembl_gene_id":"ENSG00000257414.1","gene_symbol":"OR6C73P","gene_name":"olfactory receptor family 6 subfamily C member 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:31302]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403289","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55396340,"end":55396697,"strand":1,"description":"olfactory receptor family 6 subfamily C member 73 pseudogene [Source:HGNC Symbol;Acc:HGNC:31302]"}, {"versioned_ensembl_gene_id":"ENSG00000228623.5","gene_symbol":"ZNF883","gene_name":"zinc finger protein 883 [Source:HGNC Symbol;Acc:HGNC:27271]","synonyms":null,"biotype":"protein_coding","ncbi_id":"169834","summary":null,"start":112957722,"end":113050043,"strand":-1,"description":"zinc finger protein 883 [Source:HGNC Symbol;Acc:HGNC:27271]"}, {"versioned_ensembl_gene_id":"ENSG00000164265.8","gene_symbol":"SCGB3A2","gene_name":"secretoglobin family 3A member 2 [Source:HGNC Symbol;Acc:HGNC:18391]","synonyms":"UGRP1,PNSP1,LU103","biotype":"protein_coding","ncbi_id":"117156","summary":"The protein encoded by this gene is a secreted lung surfactant protein and a downstream target of thyroid transcription factor. A single nucleotide polymorphism in the promoter of this gene results in susceptibility to asthma.[provided by RefSeq, Mar 2010]","start":147870682,"end":147882191,"strand":1,"description":"secretoglobin family 3A member 2 [Source:HGNC Symbol;Acc:HGNC:18391]"}, {"versioned_ensembl_gene_id":"ENSG00000276407.4","gene_symbol":"AC024559.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194070103,"end":194080443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008394.12","gene_symbol":"MGST1","gene_name":"microsomal glutathione S-transferase 1 [Source:HGNC Symbol;Acc:HGNC:7061]","synonyms":"MGST-I,GST12","biotype":"protein_coding","ncbi_id":"4257","summary":"The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family consists of six human proteins, two of which are involved in the production of leukotrienes and prostaglandin E, important mediators of inflammation. Other family members, demonstrating glutathione S-transferase and peroxidase activities, are involved in cellular defense against toxic, carcinogenic, and pharmacologically active electrophilic compounds. This gene encodes a protein that catalyzes the conjugation of glutathione to electrophiles and the reduction of lipid hydroperoxides. This protein is localized to the endoplasmic reticulum and outer mitochondrial membrane where it is thought to protect these membranes from oxidative stress. Several transcript variants, some non-protein coding and some protein coding, have been found for this gene. [provided by RefSeq, May 2012]","start":16347142,"end":16609259,"strand":1,"description":"microsomal glutathione S-transferase 1 [Source:HGNC Symbol;Acc:HGNC:7061]"}, {"versioned_ensembl_gene_id":"ENSG00000270799.1","gene_symbol":"AC013467.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174171891,"end":174172725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126500.3","gene_symbol":"FLRT1","gene_name":"fibronectin leucine rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:3760]","synonyms":"SPG68,MGC21624","biotype":"protein_coding","ncbi_id":"23769","summary":"This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. The family members may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. The encoded protein shares sequence similarity with two other family members, FLRT2 and FLRT3. This gene is expressed in kidney and brain. [provided by RefSeq, Jul 2008]","start":64103188,"end":64119173,"strand":1,"description":"fibronectin leucine rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:3760]"}, {"versioned_ensembl_gene_id":"ENSG00000164603.11","gene_symbol":"BMT2","gene_name":"base methyltransferase of 25S rRNA 2 homolog [Source:HGNC Symbol;Acc:HGNC:26475]","synonyms":"FLJ31818,DKFZp762M126,C7orf60","biotype":"protein_coding","ncbi_id":"154743","summary":null,"start":112819147,"end":112939916,"strand":-1,"description":"base methyltransferase of 25S rRNA 2 homolog [Source:HGNC Symbol;Acc:HGNC:26475]"}, {"versioned_ensembl_gene_id":"ENSG00000273509.1","gene_symbol":"CNTNAP3P1","gene_name":"contactin associated protein-like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49591]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420787","summary":null,"start":62924911,"end":62934964,"strand":1,"description":"contactin associated protein-like 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49591]"}, {"versioned_ensembl_gene_id":"ENSG00000235747.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"processed_transcript","ncbi_id":"102723346","summary":null,"start":30936693,"end":30945575,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000232251.5","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"C6orf37,bCX105N19.6,PBLT","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":30931715,"end":30944934,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000140564.11","gene_symbol":"FURIN","gene_name":"furin, paired basic amino acid cleaving enzyme [Source:HGNC Symbol;Acc:HGNC:8568]","synonyms":"PCSK3,PACE,FUR,SPC1","biotype":"protein_coding","ncbi_id":"5045","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. Like other members of this convertase family, the product of this gene specifically cleaves substrates at single or paired basic residues. Some of its substrates include proparathyroid hormone, transforming growth factor beta 1 precursor, proalbumin, pro-beta-secretase, membrane type-1 matrix metalloproteinase, beta subunit of pro-nerve growth factor and von Willebrand factor. It is thought to be one of the proteases responsible for the activation of HIV envelope glycoproteins gp160 and gp140, and may play a role in tumor progression. Unlike SARS-CoV and other coronaviruses, the spike protein of SARS-CoV-2 is thought to be uniquely cleaved by this protease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2020]","start":90868592,"end":90883458,"strand":1,"description":"furin, paired basic amino acid cleaving enzyme [Source:HGNC Symbol;Acc:HGNC:8568]"}, {"versioned_ensembl_gene_id":"ENSG00000128482.15","gene_symbol":"RNF112","gene_name":"ring finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12968]","synonyms":"ZNF179,BFP","biotype":"protein_coding","ncbi_id":"7732","summary":"This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":19411125,"end":19417276,"strand":1,"description":"ring finger protein 112 [Source:HGNC Symbol;Acc:HGNC:12968]"}, {"versioned_ensembl_gene_id":"ENSG00000204516.9","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31494881,"end":31511124,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000235199.1","gene_symbol":"CYP2C58P","gene_name":"cytochrome P450 family 2 subfamily C member 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:39969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480430","summary":null,"start":94865852,"end":94873129,"strand":-1,"description":"cytochrome P450 family 2 subfamily C member 58, pseudogene [Source:HGNC Symbol;Acc:HGNC:39969]"}, {"versioned_ensembl_gene_id":"ENSG00000233554.5","gene_symbol":"B4GALT1-AS1","gene_name":"B4GALT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49910]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929639","summary":null,"start":33166975,"end":33179983,"strand":1,"description":"B4GALT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49910]"}, {"versioned_ensembl_gene_id":"ENSG00000080986.12","gene_symbol":"NDC80","gene_name":"NDC80, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16909]","synonyms":"TID3,KNTC2,hsNDC80,HEC1,HEC","biotype":"protein_coding","ncbi_id":"10403","summary":"This gene encodes a component of the NDC80 kinetochore complex. The encoded protein consists of an N-terminal microtubule binding domain and a C-terminal coiled-coiled domain that interacts with other components of the complex. This protein functions to organize and stabilize microtubule-kinetochore interactions and is required for proper chromosome segregation. [provided by RefSeq, Oct 2011]","start":2571511,"end":2616635,"strand":1,"description":"NDC80, kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:16909]"}, {"versioned_ensembl_gene_id":"ENSG00000117410.13","gene_symbol":"ATP6V0B","gene_name":"ATPase H+ transporting V0 subunit b [Source:HGNC Symbol;Acc:HGNC:861]","synonyms":"HATPL,VMA16,ATP6F","biotype":"protein_coding","ncbi_id":"533","summary":"This gene encodes a portion of the V0 domain of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. Activity of this enzyme is necessary for such varied processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":43974487,"end":43978295,"strand":1,"description":"ATPase H+ transporting V0 subunit b [Source:HGNC Symbol;Acc:HGNC:861]"}, {"versioned_ensembl_gene_id":"ENSG00000278178.2","gene_symbol":"AC171558.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21659028,"end":21660224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249237.5","gene_symbol":"AL359273.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":84344678,"end":84349939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229125.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H6,OR6-2,OR2H8","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457248,"end":29464396,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000226548.1","gene_symbol":"AC016722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46852020,"end":46853496,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236841.7","gene_symbol":"AC007750.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162159762,"end":162173223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279231.1","gene_symbol":"AL356585.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18331933,"end":18348596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234906.9","gene_symbol":"APOC2","gene_name":"apolipoprotein C2 [Source:HGNC Symbol;Acc:HGNC:609]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344","summary":"This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is secreted in plasma where it is a component of very low density lipoprotein. This protein activates the enzyme lipoprotein lipase, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring upstream apolipoprotein C-IV (APOC4) gene. [provided by RefSeq, Mar 2011]","start":44945982,"end":44949565,"strand":1,"description":"apolipoprotein C2 [Source:HGNC Symbol;Acc:HGNC:609]"}, {"versioned_ensembl_gene_id":"ENSG00000249518.1","gene_symbol":"AC011352.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147851644,"end":147852659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124207.16","gene_symbol":"CSE1L","gene_name":"chromosome segregation 1 like [Source:HGNC Symbol;Acc:HGNC:2431]","synonyms":"XPO2,CSE1,CAS","biotype":"protein_coding","ncbi_id":"1434","summary":"Proteins that carry a nuclear localization signal (NLS) are transported into the nucleus by the importin-alpha/beta heterodimer. Importin-alpha binds the NLS, while importin-beta mediates translocation through the nuclear pore complex. After translocation, RanGTP binds importin-beta and displaces importin-alpha. Importin-alpha must then be returned to the cytoplasm, leaving the NLS protein behind. The protein encoded by this gene binds strongly to NLS-free importin-alpha, and this binding is released in the cytoplasm by the combined action of RANBP1 and RANGAP1. In addition, the encoded protein may play a role both in apoptosis and in cell proliferation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":49046246,"end":49096960,"strand":1,"description":"chromosome segregation 1 like [Source:HGNC Symbol;Acc:HGNC:2431]"}, {"versioned_ensembl_gene_id":"ENSG00000146067.15","gene_symbol":"FAM193B","gene_name":"family with sequence similarity 193 member B [Source:HGNC Symbol;Acc:HGNC:25524]","synonyms":"KIAA1931,IRIZIO,FLJ10404","biotype":"protein_coding","ncbi_id":"54540","summary":null,"start":177519788,"end":177554541,"strand":-1,"description":"family with sequence similarity 193 member B [Source:HGNC Symbol;Acc:HGNC:25524]"}, {"versioned_ensembl_gene_id":"ENSG00000223811.1","gene_symbol":"AL589684.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113357003,"end":113367944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272843.1","gene_symbol":"AC211476.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72924418,"end":72925125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237766.2","gene_symbol":"GGTA2P","gene_name":"glycoprotein, alpha-galactosyltransferase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:4254]","synonyms":"GLYT3,GLYT2L,GGTA1P,HGT2","biotype":"processed_pseudogene","ncbi_id":"121328","summary":null,"start":67265842,"end":67266966,"strand":-1,"description":"glycoprotein, alpha-galactosyltransferase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:4254]"}, {"versioned_ensembl_gene_id":"ENSG00000255976.1","gene_symbol":"RAB11AP2","gene_name":"RAB11A, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45189]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480447","summary":null,"start":67131567,"end":67132205,"strand":-1,"description":"RAB11A, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45189]"}, {"versioned_ensembl_gene_id":"ENSG00000168229.3","gene_symbol":"PTGDR","gene_name":"prostaglandin D2 receptor [Source:HGNC Symbol;Acc:HGNC:9591]","synonyms":"PTGDR1,DP1,DP","biotype":"protein_coding","ncbi_id":"5729","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor (GPCR) superfamily. The receptors are seven-pass transmembrane proteins that respond to extracellular cues and activate intracellular signal transduction pathways. This protein is reported to be a receptor for prostaglandin D2, which is a mediator of allergic inflammation and allergic airway inflammation in asthma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":52267713,"end":52276724,"strand":1,"description":"prostaglandin D2 receptor [Source:HGNC Symbol;Acc:HGNC:9591]"}, {"versioned_ensembl_gene_id":"ENSG00000230542.6","gene_symbol":"LINC00102","gene_name":"long intergenic non-protein coding RNA 102 [Source:HGNC Symbol;Acc:HGNC:30470]","synonyms":"OTTHUMT00000055623,NCRNA00102","biotype":"lincRNA","ncbi_id":"100359394","summary":null,"start":2612988,"end":2615347,"strand":-1,"description":"long intergenic non-protein coding RNA 102 [Source:HGNC Symbol;Acc:HGNC:30470]"}, {"versioned_ensembl_gene_id":"ENSG00000225851.1","gene_symbol":"HLA-S","gene_name":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]","synonyms":"HLA-17","biotype":"unprocessed_pseudogene","ncbi_id":"267015","summary":null,"start":31382074,"end":31382288,"strand":-1,"description":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]"}, {"versioned_ensembl_gene_id":"ENSG00000282427.1","gene_symbol":"AC243753.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14695572,"end":14707060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241281.1","gene_symbol":"AC010683.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147425974,"end":147426351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279376.1","gene_symbol":"AC092435.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":147025914,"end":147030072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229381.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"RFB30,HERF1,RNF9","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30230427,"end":30239418,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000087077.13","gene_symbol":"TRIP6","gene_name":"thyroid hormone receptor interactor 6 [Source:HGNC Symbol;Acc:HGNC:12311]","synonyms":"ZRP-1,OIP1,MGC4423,MGC3837,MGC29959,MGC10558,MGC10556","biotype":"protein_coding","ncbi_id":"7205","summary":"This gene is a member of the zyxin family and encodes a protein with three LIM zinc-binding domains. This protein localizes to focal adhesion sites and along actin stress fibers. Recruitment of this protein to the plasma membrane occurs in a lysophosphatidic acid (LPA)-dependent manner and it regulates LPA-induced cell migration. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":100867138,"end":100873454,"strand":1,"description":"thyroid hormone receptor interactor 6 [Source:HGNC Symbol;Acc:HGNC:12311]"}, {"versioned_ensembl_gene_id":"ENSG00000274828.1","gene_symbol":"AC068473.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79677287,"end":79679358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187533.13","gene_symbol":"PRR27","gene_name":"proline rich 27 [Source:HGNC Symbol;Acc:HGNC:33193]","synonyms":"C4orf40","biotype":"protein_coding","ncbi_id":"401137","summary":null,"start":70133616,"end":70176799,"strand":1,"description":"proline rich 27 [Source:HGNC Symbol;Acc:HGNC:33193]"}, {"versioned_ensembl_gene_id":"ENSG00000132958.17","gene_symbol":"TPTE2","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 [Source:HGNC Symbol;Acc:HGNC:17299]","synonyms":"TPIP","biotype":"protein_coding","ncbi_id":"93492","summary":"TPIP is a member of a large class of membrane-associated phosphatases with substrate specificity for the 3-position phosphate of inositol phospholipids.[supplied by OMIM, Jul 2002]","start":19422877,"end":19536762,"strand":-1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 [Source:HGNC Symbol;Acc:HGNC:17299]"}, {"versioned_ensembl_gene_id":"ENSG00000255188.1","gene_symbol":"AP003327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129788064,"end":129788190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000043039.6","gene_symbol":"BARX2","gene_name":"BARX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:956]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8538","summary":"This gene encodes a member of the homeobox transcription factor family. A highly related protein in mouse has been shown to influence cellular processes that control cell adhesion and remodeling of the actin cytoskeleton in myoblast fusion and chondrogenesis. The encoded protein may also play a role in cancer progression. [provided by RefSeq, Jul 2008]","start":129375940,"end":129452279,"strand":1,"description":"BARX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:956]"}, {"versioned_ensembl_gene_id":"ENSG00000230758.1","gene_symbol":"SNAP23P1","gene_name":"synaptosome associated protein 23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16561]","synonyms":"SNAP23P,dJ155G6.3","biotype":"processed_pseudogene","ncbi_id":"101290500","summary":null,"start":49038357,"end":49038602,"strand":-1,"description":"synaptosome associated protein 23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16561]"}, {"versioned_ensembl_gene_id":"ENSG00000238082.1","gene_symbol":"AC009948.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178454716,"end":178455428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225508.1","gene_symbol":"SSXP5","gene_name":"SSX family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30642]","synonyms":"psiSSX5","biotype":"unprocessed_pseudogene","ncbi_id":"326339","summary":null,"start":52672718,"end":52677051,"strand":1,"description":"SSX family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30642]"}, {"versioned_ensembl_gene_id":"ENSG00000112818.9","gene_symbol":"MEP1A","gene_name":"meprin A subunit alpha [Source:HGNC Symbol;Acc:HGNC:7015]","synonyms":"PPHA","biotype":"protein_coding","ncbi_id":"4224","summary":null,"start":46793390,"end":46839782,"strand":1,"description":"meprin A subunit alpha [Source:HGNC Symbol;Acc:HGNC:7015]"}, {"versioned_ensembl_gene_id":"ENSG00000205044.4","gene_symbol":"AC027369.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49009959,"end":49015894,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174705.12","gene_symbol":"SH3PXD2B","gene_name":"SH3 and PX domains 2B [Source:HGNC Symbol;Acc:HGNC:29242]","synonyms":"KIAA1295,FLJ20831","biotype":"protein_coding","ncbi_id":"285590","summary":"This gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), and also Borrone Dermato-Cardio-Skeletal (BDCS) syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":172325000,"end":172454523,"strand":-1,"description":"SH3 and PX domains 2B [Source:HGNC Symbol;Acc:HGNC:29242]"}, {"versioned_ensembl_gene_id":"ENSG00000145335.15","gene_symbol":"SNCA","gene_name":"synuclein alpha [Source:HGNC Symbol;Acc:HGNC:11138]","synonyms":"PD1,PARK4,PARK1,NACP","biotype":"protein_coding","ncbi_id":"6622","summary":"Alpha-synuclein is a member of the synuclein family, which also includes beta- and gamma-synuclein. Synucleins are abundantly expressed in the brain and alpha- and beta-synuclein inhibit phospholipase D2 selectively. SNCA may serve to integrate presynaptic signaling and membrane trafficking. Defects in SNCA have been implicated in the pathogenesis of Parkinson disease. SNCA peptides are a major component of amyloid plaques in the brains of patients with Alzheimer's disease. Alternatively spliced transcripts encoding different isoforms have been identified for this gene. [provided by RefSeq, Feb 2016]","start":89724099,"end":89838315,"strand":-1,"description":"synuclein alpha [Source:HGNC Symbol;Acc:HGNC:11138]"}, {"versioned_ensembl_gene_id":"ENSG00000204195.3","gene_symbol":"AWAT1","gene_name":"acyl-CoA wax alcohol acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23252]","synonyms":"DGAT2L3","biotype":"protein_coding","ncbi_id":"158833","summary":"The protein encoded by this gene belongs to the diacylglycerol acyltransferase family. It esterifies long chain (wax) alcohols with acyl-CoA-derived fatty acids to produce wax esters. Wax esters are enriched in sebum, suggesting that this enzyme plays a central role in lipid metabolism in skin. Consistent with this observation, this protein is predominantly expressed in the sebaceous gland of the skin. [provided by RefSeq, Sep 2009]","start":70234655,"end":70240627,"strand":1,"description":"acyl-CoA wax alcohol acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23252]"}, {"versioned_ensembl_gene_id":"ENSG00000226647.2","gene_symbol":"AL365356.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5712174,"end":5744067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229599.1","gene_symbol":"LINC00411","gene_name":"long intergenic non-protein coding RNA 411 [Source:HGNC Symbol;Acc:HGNC:42744]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874161","summary":null,"start":100940862,"end":100944364,"strand":-1,"description":"long intergenic non-protein coding RNA 411 [Source:HGNC Symbol;Acc:HGNC:42744]"}, {"versioned_ensembl_gene_id":"ENSG00000149090.11","gene_symbol":"PAMR1","gene_name":"peptidase domain containing associated with muscle regeneration 1 [Source:HGNC Symbol;Acc:HGNC:24554]","synonyms":"RAMP,DKFZP586H2123","biotype":"protein_coding","ncbi_id":"25891","summary":null,"start":35431823,"end":35530300,"strand":-1,"description":"peptidase domain containing associated with muscle regeneration 1 [Source:HGNC Symbol;Acc:HGNC:24554]"}, {"versioned_ensembl_gene_id":"ENSG00000132670.20","gene_symbol":"PTPRA","gene_name":"protein tyrosine phosphatase, receptor type A [Source:HGNC Symbol;Acc:HGNC:9664]","synonyms":"RPTPA,PTPRL2,PTPA,LRP,HPTPA,HLPR","biotype":"protein_coding","ncbi_id":"5786","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. This PTP has been shown to dephosphorylate and activate Src family tyrosine kinases, and is implicated in the regulation of integrin signaling, cell adhesion and proliferation. Three alternatively spliced variants of this gene, which encode two distinct isoforms, have been reported. [provided by RefSeq, Jul 2008]","start":2864184,"end":3039076,"strand":1,"description":"protein tyrosine phosphatase, receptor type A [Source:HGNC Symbol;Acc:HGNC:9664]"}, {"versioned_ensembl_gene_id":"ENSG00000237993.1","gene_symbol":"AL365318.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116013813,"end":116017705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264608.1","gene_symbol":"AC005726.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28601827,"end":28602284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164855.15","gene_symbol":"TMEM184A","gene_name":"transmembrane protein 184A [Source:HGNC Symbol;Acc:HGNC:28797]","synonyms":"SDMG1,MGC9712","biotype":"protein_coding","ncbi_id":"202915","summary":null,"start":1542235,"end":1560821,"strand":-1,"description":"transmembrane protein 184A [Source:HGNC Symbol;Acc:HGNC:28797]"}, {"versioned_ensembl_gene_id":"ENSG00000169715.14","gene_symbol":"MT1E","gene_name":"metallothionein 1E [Source:HGNC Symbol;Acc:HGNC:7397]","synonyms":"MTD,MT1","biotype":"protein_coding","ncbi_id":"4493","summary":null,"start":56625475,"end":56627112,"strand":1,"description":"metallothionein 1E [Source:HGNC Symbol;Acc:HGNC:7397]"}, {"versioned_ensembl_gene_id":"ENSG00000171757.15","gene_symbol":"LRRC34","gene_name":"leucine rich repeat containing 34 [Source:HGNC Symbol;Acc:HGNC:28408]","synonyms":"MGC27085","biotype":"protein_coding","ncbi_id":"151827","summary":null,"start":169793428,"end":169812986,"strand":-1,"description":"leucine rich repeat containing 34 [Source:HGNC Symbol;Acc:HGNC:28408]"}, {"versioned_ensembl_gene_id":"ENSG00000236496.2","gene_symbol":"GPS2P1","gene_name":"G protein pathway suppressor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392281","summary":null,"start":2875442,"end":2876427,"strand":-1,"description":"G protein pathway suppressor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49622]"}, {"versioned_ensembl_gene_id":"ENSG00000227941.1","gene_symbol":"UQCRBP2","gene_name":"ubiquinol-cytochrome c reductase binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12584]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130719","summary":null,"start":162541332,"end":162541628,"strand":-1,"description":"ubiquinol-cytochrome c reductase binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12584]"}, {"versioned_ensembl_gene_id":"ENSG00000270555.1","gene_symbol":"AC211469.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72768798,"end":72769191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120055.7","gene_symbol":"C10orf95","gene_name":"chromosome 10 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:25880]","synonyms":"FLJ14280","biotype":"protein_coding","ncbi_id":"79946","summary":null,"start":102449837,"end":102451543,"strand":-1,"description":"chromosome 10 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:25880]"}, {"versioned_ensembl_gene_id":"ENSG00000220418.1","gene_symbol":"TUBB3P1","gene_name":"tubulin beta 3 class III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288513","summary":null,"start":89301783,"end":89303114,"strand":1,"description":"tubulin beta 3 class III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42339]"}, {"versioned_ensembl_gene_id":"ENSG00000206447.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31518986,"end":31520501,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000268333.1","gene_symbol":"AL132655.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58833809,"end":58836529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204379.10","gene_symbol":"XAGE1A","gene_name":"X antigen family member 1A [Source:HGNC Symbol;Acc:HGNC:4111]","synonyms":"XAGE1,XAGE-1,GAGED2,CT12.1a","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52495676,"end":52500812,"strand":1,"description":"X antigen family member 1A [Source:HGNC Symbol;Acc:HGNC:4111]"}, {"versioned_ensembl_gene_id":"ENSG00000212951.5","gene_symbol":"BX005266.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62532397,"end":62532853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250084.1","gene_symbol":"BX510359.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52448587,"end":52451138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244255.5","gene_symbol":"AL645922.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31927698,"end":31952048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276897.1","gene_symbol":"AC231532.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52409772,"end":52410432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239939.1","gene_symbol":"RPSAP34","gene_name":"ribosomal protein SA pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36643]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270876","summary":null,"start":108407843,"end":108408578,"strand":-1,"description":"ribosomal protein SA pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36643]"}, {"versioned_ensembl_gene_id":"ENSG00000274567.1","gene_symbol":"AC144587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69469588,"end":69469841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260274.1","gene_symbol":"AC068338.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75368155,"end":75369584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255215.1","gene_symbol":"OR4R1P","gene_name":"olfactory receptor family 4 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14798]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79528","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48486363,"end":48486825,"strand":-1,"description":"olfactory receptor family 4 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14798]"}, {"versioned_ensembl_gene_id":"ENSG00000259242.2","gene_symbol":"AC002306.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19606350,"end":19608660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249307.5","gene_symbol":"LINC01088","gene_name":"long intergenic non-protein coding RNA 1088 [Source:HGNC Symbol;Acc:HGNC:49148]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505875","summary":null,"start":78971748,"end":79308798,"strand":1,"description":"long intergenic non-protein coding RNA 1088 [Source:HGNC Symbol;Acc:HGNC:49148]"}, {"versioned_ensembl_gene_id":"ENSG00000161849.3","gene_symbol":"KRT84","gene_name":"keratin 84 [Source:HGNC Symbol;Acc:HGNC:6461]","synonyms":"KRTHB4,Hb-4","biotype":"protein_coding","ncbi_id":"3890","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin is contained primarily in the filiform tongue papilla, among other hair keratins. [provided by RefSeq, Jul 2008]","start":52377812,"end":52385652,"strand":-1,"description":"keratin 84 [Source:HGNC Symbol;Acc:HGNC:6461]"}, {"versioned_ensembl_gene_id":"ENSG00000267687.1","gene_symbol":"AC010928.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60525616,"end":60526156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250343.1","gene_symbol":"STK32A-AS1","gene_name":"STK32A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53468]","synonyms":"CTC-255N20","biotype":"antisense_RNA","ncbi_id":"105378217","summary":null,"start":147180204,"end":147234859,"strand":-1,"description":"STK32A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53468]"}, {"versioned_ensembl_gene_id":"ENSG00000229572.1","gene_symbol":"EIF4BP4","gene_name":"eukaryotic translation initiation factor 4B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130064","summary":null,"start":42340588,"end":42342367,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37937]"}, {"versioned_ensembl_gene_id":"ENSG00000233747.1","gene_symbol":"RPL36AP13","gene_name":"ribosomal protein L36a pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35877]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271323","summary":null,"start":24334512,"end":24335152,"strand":1,"description":"ribosomal protein L36a pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35877]"}, {"versioned_ensembl_gene_id":"ENSG00000231280.1","gene_symbol":"SALL4P6","gene_name":"spalt like transcription factor 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39823]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391530","summary":null,"start":42321005,"end":42322695,"strand":1,"description":"spalt like transcription factor 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39823]"}, {"versioned_ensembl_gene_id":"ENSG00000275756.1","gene_symbol":"AL354751.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92104425,"end":92105451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138380.17","gene_symbol":"CARF","gene_name":"calcium responsive transcription factor [Source:HGNC Symbol;Acc:HGNC:14435]","synonyms":"NYD-SP24,FLJ21579,CaRF,ALS2CR8","biotype":"protein_coding","ncbi_id":"79800","summary":null,"start":202912214,"end":202987063,"strand":1,"description":"calcium responsive transcription factor [Source:HGNC Symbol;Acc:HGNC:14435]"}, {"versioned_ensembl_gene_id":"ENSG00000204801.7","gene_symbol":"FGF7P7","gene_name":"fibroblast growth factor 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33589]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728433","summary":null,"start":62474948,"end":62476333,"strand":-1,"description":"fibroblast growth factor 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33589]"}, {"versioned_ensembl_gene_id":"ENSG00000176406.22","gene_symbol":"RIMS2","gene_name":"regulating synaptic membrane exocytosis 2 [Source:HGNC Symbol;Acc:HGNC:17283]","synonyms":"RIM2,RAB3IP3,OBOE,KIAA0751","biotype":"protein_coding","ncbi_id":"9699","summary":"The protein encoded by this gene is a presynaptic protein that interacts with RAB3, a protein important for normal neurotransmitter release. The encoded protein can also bind several other synaptic proteins, including UNC-13 homolog B, ELKS/Rab6-interacting/CAST family member 1, and synaptotagmin 1. This protein is involved in synaptic membrane exocytosis. Polymorphisms in this gene have been associated with degenerative lumbar scoliosis. [provided by RefSeq, Feb 2017]","start":103500748,"end":104256094,"strand":1,"description":"regulating synaptic membrane exocytosis 2 [Source:HGNC Symbol;Acc:HGNC:17283]"}, {"versioned_ensembl_gene_id":"ENSG00000254644.1","gene_symbol":"AC007751.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103568603,"end":103568978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225038.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30183722,"end":30193204,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000258472.8","gene_symbol":"AC005726.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28455752,"end":28614197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272335.1","gene_symbol":"AC093297.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44826076,"end":44828592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131183.10","gene_symbol":"SLC34A1","gene_name":"solute carrier family 34 member 1 [Source:HGNC Symbol;Acc:HGNC:11019]","synonyms":"NAPI-3,SLC17A2,SLC11,NPTIIa,NPT2","biotype":"protein_coding","ncbi_id":"6569","summary":"This gene encodes a member of the type II sodium-phosphate cotransporter family. Mutations in this gene are associated with hypophosphatemia nephrolithiasis/osteoporosis 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":177379235,"end":177398848,"strand":1,"description":"solute carrier family 34 member 1 [Source:HGNC Symbol;Acc:HGNC:11019]"}, {"versioned_ensembl_gene_id":"ENSG00000227498.2","gene_symbol":"AC018359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34524818,"end":34543880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228861.5","gene_symbol":"RPL23AP12","gene_name":"ribosomal protein L23a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:23840]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391282","summary":null,"start":39127568,"end":39128040,"strand":1,"description":"ribosomal protein L23a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:23840]"}, {"versioned_ensembl_gene_id":"ENSG00000237994.1","gene_symbol":"AC003659.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28942050,"end":28942568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169306.9","gene_symbol":"IL1RAPL1","gene_name":"interleukin 1 receptor accessory protein like 1 [Source:HGNC Symbol;Acc:HGNC:5996]","synonyms":"TIGIRR-2,OPHN4,MRX34,MRX21,MRX10,IL1RAPL,IL1R8","biotype":"protein_coding","ncbi_id":"11141","summary":"The protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. This protein has an N-terminal signal peptide, three extracellular immunoglobulin Ig-like domains, a transmembrane domain, an intracellular Toll/IL-1R domain, and a long C-terminal tail which interacts with multiple signalling molecules. This gene is located at a region on chromosome X that is associated with a non-syndromic form of X-linked intellectual disability. Deletions and mutations in this gene were found in patients with intellectual disability. This gene is expressed at a high level in post-natal brain structures involved in the hippocampal memory system, which suggests a specialized role in the physiological processes underlying memory and learning abilities, and plays a role in synapse formation and stabilization. [provided by RefSeq, Jul 2017]","start":28587399,"end":29956723,"strand":1,"description":"interleukin 1 receptor accessory protein like 1 [Source:HGNC Symbol;Acc:HGNC:5996]"}, {"versioned_ensembl_gene_id":"ENSG00000237620.1","gene_symbol":"GCNT1P5","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37975]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421598","summary":null,"start":77461458,"end":77462139,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37975]"}, {"versioned_ensembl_gene_id":"ENSG00000259941.1","gene_symbol":"AC084782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56394321,"end":56396785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267454.5","gene_symbol":"ZNF582-AS1","gene_name":"ZNF582 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:25213]","synonyms":null,"biotype":"lincRNA","ncbi_id":"386758","summary":null,"start":56393656,"end":56399172,"strand":1,"description":"ZNF582 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:25213]"}, {"versioned_ensembl_gene_id":"ENSG00000230336.9","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"MGC22487,Oct4,OCT3,OTF3","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31209245,"end":31215620,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000118162.13","gene_symbol":"KPTN","gene_name":"kaptin, actin binding protein [Source:HGNC Symbol;Acc:HGNC:6404]","synonyms":"2.00E+04","biotype":"protein_coding","ncbi_id":"11133","summary":"This gene encodes a filamentous-actin-associated protein, which is involved in actin dynamics and plays an important role in neuromorphogenesis. This protein is part of the KICSTOR protein complex that localizes to lysosomes. Mutations in this gene result in an autosomal recessive form of intellectual disability. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2017]","start":47475144,"end":47484268,"strand":-1,"description":"kaptin, actin binding protein [Source:HGNC Symbol;Acc:HGNC:6404]"}, {"versioned_ensembl_gene_id":"ENSG00000162972.10","gene_symbol":"MAIP1","gene_name":"matrix AAA peptidase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26198]","synonyms":"FLJ22555,DKFZp666A212,C2orf47","biotype":"protein_coding","ncbi_id":"79568","summary":null,"start":199955317,"end":200008540,"strand":1,"description":"matrix AAA peptidase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26198]"}, {"versioned_ensembl_gene_id":"ENSG00000226287.8","gene_symbol":"TMEM191A","gene_name":"transmembrane protein 191A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:25317]","synonyms":"TMEM191AP,DKFZp434N035","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"84222","summary":null,"start":20701114,"end":20704606,"strand":1,"description":"transmembrane protein 191A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:25317]"}, {"versioned_ensembl_gene_id":"ENSG00000261693.1","gene_symbol":"AC134682.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142403652,"end":142407028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229788.1","gene_symbol":"LINC00388","gene_name":"long intergenic non-protein coding RNA 388 [Source:HGNC Symbol;Acc:HGNC:42716]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874153","summary":null,"start":18610298,"end":18611675,"strand":-1,"description":"long intergenic non-protein coding RNA 388 [Source:HGNC Symbol;Acc:HGNC:42716]"}, {"versioned_ensembl_gene_id":"ENSG00000147852.15","gene_symbol":"VLDLR","gene_name":"very low density lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:12698]","synonyms":"VLDLRCH,CHRMQ1,CARMQ1","biotype":"protein_coding","ncbi_id":"7436","summary":"The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq, Aug 2009]","start":2621834,"end":2660053,"strand":1,"description":"very low density lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:12698]"}, {"versioned_ensembl_gene_id":"ENSG00000272514.5","gene_symbol":"CFAP206","gene_name":"cilia and flagella associated protein 206 [Source:HGNC Symbol;Acc:HGNC:21405]","synonyms":"FLJ25974,dJ382I10.1,C6orf165","biotype":"protein_coding","ncbi_id":"154313","summary":null,"start":87407983,"end":87464465,"strand":1,"description":"cilia and flagella associated protein 206 [Source:HGNC Symbol;Acc:HGNC:21405]"}, {"versioned_ensembl_gene_id":"ENSG00000267453.7","gene_symbol":"LINC01835","gene_name":"long intergenic non-protein coding RNA 1835 [Source:HGNC Symbol;Acc:HGNC:52651]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"102724279","summary":null,"start":15851993,"end":15864904,"strand":-1,"description":"long intergenic non-protein coding RNA 1835 [Source:HGNC Symbol;Acc:HGNC:52651]"}, {"versioned_ensembl_gene_id":"ENSG00000178301.3","gene_symbol":"AQP11","gene_name":"aquaporin 11 [Source:HGNC Symbol;Acc:HGNC:19940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282679","summary":null,"start":77589391,"end":77610355,"strand":1,"description":"aquaporin 11 [Source:HGNC Symbol;Acc:HGNC:19940]"}, {"versioned_ensembl_gene_id":"ENSG00000250727.1","gene_symbol":"AC100871.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124141888,"end":124143512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147316.12","gene_symbol":"MCPH1","gene_name":"microcephalin 1 [Source:HGNC Symbol;Acc:HGNC:6954]","synonyms":"BRIT1,FLJ12847","biotype":"protein_coding","ncbi_id":"79648","summary":"This gene encodes a DNA damage response protein. The encoded protein may play a role in G2/M checkpoint arrest via maintenance of inhibitory phosphorylation of cyclin-dependent kinase 1. Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]","start":6406592,"end":6648504,"strand":1,"description":"microcephalin 1 [Source:HGNC Symbol;Acc:HGNC:6954]"}, {"versioned_ensembl_gene_id":"ENSG00000121417.13","gene_symbol":"ZNF211","gene_name":"zinc finger protein 211 [Source:HGNC Symbol;Acc:HGNC:13003]","synonyms":"ZNF-25,CH2H2-25","biotype":"protein_coding","ncbi_id":"10520","summary":"This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. This protein may play a role in developmental processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":57630395,"end":57642779,"strand":1,"description":"zinc finger protein 211 [Source:HGNC Symbol;Acc:HGNC:13003]"}, {"versioned_ensembl_gene_id":"ENSG00000271384.1","gene_symbol":"AL161729.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95406990,"end":95407662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230221.2","gene_symbol":"AL157384.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95292338,"end":95294810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270766.1","gene_symbol":"AC024940.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31244440,"end":31244685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179909.15","gene_symbol":"ZNF154","gene_name":"zinc finger protein 154 [Source:HGNC Symbol;Acc:HGNC:12939]","synonyms":"pHZ-92","biotype":"protein_coding","ncbi_id":"7710","summary":"This gene encodes a protein that belongs to the zinc finger Kruppel family of transcriptional regulators, whose members are thought to function in normal and abnormal cell growth and differentiation. Hypermethylation of this gene is associated with the recurrence of non muscle invasive bladder cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":57697367,"end":57709194,"strand":-1,"description":"zinc finger protein 154 [Source:HGNC Symbol;Acc:HGNC:12939]"}, {"versioned_ensembl_gene_id":"ENSG00000250207.1","gene_symbol":"AC079776.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":129992602,"end":129993105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272953.1","gene_symbol":"AC092171.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5425770,"end":5426401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079689.13","gene_symbol":"SCGN","gene_name":"secretagogin, EF-hand calcium binding protein [Source:HGNC Symbol;Acc:HGNC:16941]","synonyms":"SEGN,SECRET,DJ501N12.8,CALBL","biotype":"protein_coding","ncbi_id":"10590","summary":"The encoded protein is a secreted calcium-binding protein which is found in the cytoplasm. It is related to calbindin D-28K and calretinin. This protein is thought to be involved in KCL-stimulated calcium flux and cell proliferation. [provided by RefSeq, Jul 2008]","start":25652201,"end":25701783,"strand":1,"description":"secretagogin, EF-hand calcium binding protein [Source:HGNC Symbol;Acc:HGNC:16941]"}, {"versioned_ensembl_gene_id":"ENSG00000137077.7","gene_symbol":"CCL21","gene_name":"C-C motif chemokine ligand 21 [Source:HGNC Symbol;Acc:HGNC:10620]","synonyms":"TCA4,SLC,SCYA21,exodus-2,ECL,CKb9,6Ckine","biotype":"protein_coding","ncbi_id":"6366","summary":"This antimicrobial gene is one of several CC cytokine genes clustered on the p-arm of chromosome 9. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. Similar to other chemokines the protein encoded by this gene inhibits hemopoiesis and stimulates chemotaxis. This protein is chemotactic in vitro for thymocytes and activated T cells, but not for B cells, macrophages, or neutrophils. The cytokine encoded by this gene may also play a role in mediating homing of lymphocytes to secondary lymphoid organs. It is a high affinity functional ligand for chemokine receptor 7 that is expressed on T and B lymphocytes and a known receptor for another member of the cytokine family (small inducible cytokine A19). [provided by RefSeq, Sep 2014]","start":34709005,"end":34710124,"strand":-1,"description":"C-C motif chemokine ligand 21 [Source:HGNC Symbol;Acc:HGNC:10620]"}, {"versioned_ensembl_gene_id":"ENSG00000254007.1","gene_symbol":"AC084768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5659679,"end":5670077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205707.10","gene_symbol":"ETFRF1","gene_name":"electron transfer flavoprotein regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:27052]","synonyms":"LYRM5","biotype":"protein_coding","ncbi_id":"144363","summary":null,"start":25195216,"end":25209645,"strand":1,"description":"electron transfer flavoprotein regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:27052]"}, {"versioned_ensembl_gene_id":"ENSG00000253560.1","gene_symbol":"AC013643.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27697217,"end":27697526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165548.10","gene_symbol":"TMEM63C","gene_name":"transmembrane protein 63C [Source:HGNC Symbol;Acc:HGNC:23787]","synonyms":"hsCSC1,DKFZp434P0111,CSC1,C14orf171","biotype":"protein_coding","ncbi_id":"57156","summary":null,"start":77116568,"end":77259495,"strand":1,"description":"transmembrane protein 63C [Source:HGNC Symbol;Acc:HGNC:23787]"}, {"versioned_ensembl_gene_id":"ENSG00000046651.14","gene_symbol":"OFD1","gene_name":"OFD1, centriole and centriolar satellite protein [Source:HGNC Symbol;Acc:HGNC:2567]","synonyms":"RP23,JBTS10,CXorf5,71-7A","biotype":"protein_coding","ncbi_id":"8481","summary":"This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. [provided by RefSeq, Aug 2016]","start":13734745,"end":13769353,"strand":1,"description":"OFD1, centriole and centriolar satellite protein [Source:HGNC Symbol;Acc:HGNC:2567]"}, {"versioned_ensembl_gene_id":"ENSG00000255829.1","gene_symbol":"AC092490.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8664011,"end":8669011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101811.13","gene_symbol":"CSTF2","gene_name":"cleavage stimulation factor subunit 2 [Source:HGNC Symbol;Acc:HGNC:2484]","synonyms":"CstF-64","biotype":"protein_coding","ncbi_id":"1478","summary":"This gene encodes a nuclear protein with an RRM (RNA recognition motif) domain. The protein is a member of the cleavage stimulation factor (CSTF) complex that is involved in the 3' end cleavage and polyadenylation of pre-mRNAs. Specifically, this protein binds GU-rich elements within the 3'-untranslated region of mRNAs. [provided by RefSeq, Jul 2008]","start":100820359,"end":100840932,"strand":1,"description":"cleavage stimulation factor subunit 2 [Source:HGNC Symbol;Acc:HGNC:2484]"}, {"versioned_ensembl_gene_id":"ENSG00000125843.10","gene_symbol":"AP5S1","gene_name":"adaptor related protein complex 5 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:15875]","synonyms":"FLJ11168,C20orf29","biotype":"protein_coding","ncbi_id":"55317","summary":null,"start":3820524,"end":3828837,"strand":1,"description":"adaptor related protein complex 5 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:15875]"}, {"versioned_ensembl_gene_id":"ENSG00000170892.10","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"SEN34L,LENG5,LENG5,SEN34,SEN34,SEN34L","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54189938,"end":54194536,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000231586.2","gene_symbol":"RPS23P9","gene_name":"ribosomal protein S23 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48341]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419472","summary":null,"start":161617992,"end":161619585,"strand":-1,"description":"ribosomal protein S23 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48341]"}, {"versioned_ensembl_gene_id":"ENSG00000132141.13","gene_symbol":"CCT6B","gene_name":"chaperonin containing TCP1 subunit 6B [Source:HGNC Symbol;Acc:HGNC:1621]","synonyms":"TSA303,Cctz2","biotype":"protein_coding","ncbi_id":"10693","summary":"This gene encodes a molecular chaperone that is a member of the chaperonin-containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":34927859,"end":34981078,"strand":-1,"description":"chaperonin containing TCP1 subunit 6B [Source:HGNC Symbol;Acc:HGNC:1621]"}, {"versioned_ensembl_gene_id":"ENSG00000237593.1","gene_symbol":"AL445220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154216931,"end":154217489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277684.1","gene_symbol":"AL392048.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48340797,"end":48341330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136720.6","gene_symbol":"HS6ST1","gene_name":"heparan sulfate 6-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5201]","synonyms":"HS6ST","biotype":"protein_coding","ncbi_id":"9394","summary":"The protein encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biological activities. This enzyme is a type II integral membrane protein and is responsible for 6-O-sulfation of heparan sulfate. This enzyme does not share significant sequence similarity with other known sulfotransferases. A pseudogene located on chromosome 1 has been found for this gene. [provided by RefSeq, Jul 2008]","start":128236716,"end":128318577,"strand":-1,"description":"heparan sulfate 6-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5201]"}, {"versioned_ensembl_gene_id":"ENSG00000249258.2","gene_symbol":"AC079193.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17131181,"end":17149789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270926.1","gene_symbol":"AC008013.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31105105,"end":31106830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282454.1","gene_symbol":"AC023315.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36941879,"end":36945288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263505.1","gene_symbol":"AP005265.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1159198,"end":1160404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167595.14","gene_symbol":"PROSER3","gene_name":"proline and serine rich 3 [Source:HGNC Symbol;Acc:HGNC:25204]","synonyms":"FLJ30657,C19orf55","biotype":"protein_coding","ncbi_id":"148137","summary":null,"start":35758143,"end":35771028,"strand":1,"description":"proline and serine rich 3 [Source:HGNC Symbol;Acc:HGNC:25204]"}, {"versioned_ensembl_gene_id":"ENSG00000250129.5","gene_symbol":"AC116424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131053317,"end":131072339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248859.2","gene_symbol":"LINC01574","gene_name":"long intergenic non-protein coding RNA 1574 [Source:HGNC Symbol;Acc:HGNC:51388]","synonyms":"TCONS_00009551,HI-LNC12","biotype":"lincRNA","ncbi_id":"102577424","summary":null,"start":176743205,"end":176743871,"strand":1,"description":"long intergenic non-protein coding RNA 1574 [Source:HGNC Symbol;Acc:HGNC:51388]"}, {"versioned_ensembl_gene_id":"ENSG00000103089.8","gene_symbol":"FA2H","gene_name":"fatty acid 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:21197]","synonyms":"SPG35,FLJ25287,FAXDC1,FAAH","biotype":"protein_coding","ncbi_id":"79152","summary":"This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.[provided by RefSeq, Mar 2010]","start":74712955,"end":74774831,"strand":-1,"description":"fatty acid 2-hydroxylase [Source:HGNC Symbol;Acc:HGNC:21197]"}, {"versioned_ensembl_gene_id":"ENSG00000253291.1","gene_symbol":"TRBV7-7","gene_name":"T-cell receptor beta variable 7-7 [Source:HGNC Symbol;Acc:HGNC:12241]","synonyms":"TRBV77,TCRBV7S7,TCRBV6S6A2T","biotype":"TR_V_gene","ncbi_id":"28591","summary":null,"start":142511626,"end":142512127,"strand":1,"description":"T-cell receptor beta variable 7-7 [Source:HGNC Symbol;Acc:HGNC:12241]"}, {"versioned_ensembl_gene_id":"ENSG00000197322.3","gene_symbol":"C17orf102","gene_name":"chromosome 17 open reading frame 102 [Source:HGNC Symbol;Acc:HGNC:34412]","synonyms":"FLJ44815","biotype":"bidirectional_promoter_lncRNA","ncbi_id":"400591","summary":null,"start":34574123,"end":34579369,"strand":-1,"description":"chromosome 17 open reading frame 102 [Source:HGNC Symbol;Acc:HGNC:34412]"}, {"versioned_ensembl_gene_id":"ENSG00000150551.10","gene_symbol":"LYPD1","gene_name":"LY6/PLAUR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28431]","synonyms":"MGC29643,LYPDC1","biotype":"protein_coding","ncbi_id":"116372","summary":null,"start":132644853,"end":132671579,"strand":-1,"description":"LY6/PLAUR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28431]"}, {"versioned_ensembl_gene_id":"ENSG00000139998.14","gene_symbol":"RAB15","gene_name":"RAB15, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:20150]","synonyms":null,"biotype":"protein_coding","ncbi_id":"376267","summary":null,"start":64945814,"end":64972776,"strand":-1,"description":"RAB15, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:20150]"}, {"versioned_ensembl_gene_id":"ENSG00000100625.8","gene_symbol":"SIX4","gene_name":"SIX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:10890]","synonyms":"AREC3","biotype":"protein_coding","ncbi_id":"51804","summary":"This gene encodes a member of the homeobox family, subfamily SIX. The drosophila homolog is a nuclear homeoprotein required for eye development. Studies in mouse show that this gene product functions as a transcription factor, and may have a role in the differentiation or maturation of neuronal cells. [provided by RefSeq, May 2010]","start":60709528,"end":60724348,"strand":-1,"description":"SIX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:10890]"}, {"versioned_ensembl_gene_id":"ENSG00000233424.2","gene_symbol":"BX664718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42707800,"end":42714539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225774.2","gene_symbol":"SIRPAP1","gene_name":"signal regulatory protein alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9663]","synonyms":"SIRPA2P,PTPNS1L","biotype":"processed_pseudogene","ncbi_id":"23755","summary":null,"start":30542536,"end":30544305,"strand":1,"description":"signal regulatory protein alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9663]"}, {"versioned_ensembl_gene_id":"ENSG00000135413.8","gene_symbol":"LACRT","gene_name":"lacritin [Source:HGNC Symbol;Acc:HGNC:16430]","synonyms":"LACRITIN","biotype":"protein_coding","ncbi_id":"90070","summary":"The protein encoded by this gene is highly expressed in the lacrimal glands and localized primarily to secretory granules and secretory fluid. It augments lacrimal acinar cell secretion, promotes ductal cell proliferation, and stimulates signaling through tyrosine phosphorylation and release of calcium. [provided by RefSeq, Jul 2008]","start":54630811,"end":54634895,"strand":-1,"description":"lacritin [Source:HGNC Symbol;Acc:HGNC:16430]"}, {"versioned_ensembl_gene_id":"ENSG00000198738.4","gene_symbol":"SMIM11P1","gene_name":"small integral membrane protein 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21400]","synonyms":"FAM165A,C6orf161,bA33E24.4","biotype":"processed_pseudogene","ncbi_id":"100127905","summary":null,"start":85735744,"end":85735921,"strand":-1,"description":"small integral membrane protein 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21400]"}, {"versioned_ensembl_gene_id":"ENSG00000181227.3","gene_symbol":"DLSTP1","gene_name":"dihydrolipoamide S-succinyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2912]","synonyms":"DLSTP","biotype":"processed_pseudogene","ncbi_id":"1744","summary":null,"start":75743423,"end":75744776,"strand":-1,"description":"dihydrolipoamide S-succinyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2912]"}, {"versioned_ensembl_gene_id":"ENSG00000277322.1","gene_symbol":"GOLGA6L6","gene_name":"golgin A6 family-like 6 [Source:HGNC Symbol;Acc:HGNC:37225]","synonyms":"FLJ36131","biotype":"protein_coding","ncbi_id":"727832","summary":null,"start":20531856,"end":20541800,"strand":-1,"description":"golgin A6 family-like 6 [Source:HGNC Symbol;Acc:HGNC:37225]"}, {"versioned_ensembl_gene_id":"ENSG00000136574.17","gene_symbol":"GATA4","gene_name":"GATA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:4173]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2626","summary":"This gene encodes a member of the GATA family of zinc-finger transcription factors. Members of this family recognize the GATA motif which is present in the promoters of many genes. This protein is thought to regulate genes involved in embryogenesis and in myocardial differentiation and function, and is necessary for normal testicular development. Mutations in this gene have been associated with cardiac septal defects. Additionally, alterations in gene expression have been associated with several cancer types. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":11676959,"end":11760002,"strand":1,"description":"GATA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:4173]"}, {"versioned_ensembl_gene_id":"ENSG00000217334.1","gene_symbol":"AL355615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85731371,"end":85732011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235862.2","gene_symbol":"AL590648.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":212624284,"end":212626771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213881.3","gene_symbol":"NPM1P6","gene_name":"nucleophosmin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:7926]","synonyms":"NPMP6,NG6-4","biotype":"processed_pseudogene","ncbi_id":"4875","summary":null,"start":61202350,"end":61203220,"strand":1,"description":"nucleophosmin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:7926]"}, {"versioned_ensembl_gene_id":"ENSG00000123594.5","gene_symbol":"ATXN3L","gene_name":"ataxin 3 like [Source:HGNC Symbol;Acc:HGNC:24173]","synonyms":"MJDL","biotype":"protein_coding","ncbi_id":"92552","summary":"This intronless gene may be a pseudogene (PMID:11450850). This gene is similar to the multi-exon gene which encodes ataxin 3 and contains a coding region which could encode a protein similar to ataxin 3. Mutations in the gene encoding ataxin 3 are associated with Machado-Joseph disease. [provided by RefSeq, Sep 2011]","start":13318236,"end":13320399,"strand":-1,"description":"ataxin 3 like [Source:HGNC Symbol;Acc:HGNC:24173]"}, {"versioned_ensembl_gene_id":"ENSG00000231575.1","gene_symbol":"AL139118.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":94109116,"end":94121107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275102.2","gene_symbol":"OR2T5","gene_name":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401993","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248491033,"end":248491980,"strand":1,"description":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]"}, {"versioned_ensembl_gene_id":"ENSG00000164645.2","gene_symbol":"TEX47","gene_name":"testis expressed 47 [Source:HGNC Symbol;Acc:HGNC:22402]","synonyms":"MGC26647,C7orf62","biotype":"protein_coding","ncbi_id":"219557","summary":null,"start":88794106,"end":88795721,"strand":-1,"description":"testis expressed 47 [Source:HGNC Symbol;Acc:HGNC:22402]"}, {"versioned_ensembl_gene_id":"ENSG00000259111.1","gene_symbol":"AL079307.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51750560,"end":51763114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198535.5","gene_symbol":"C2CD4A","gene_name":"C2 calcium dependent domain containing 4A [Source:HGNC Symbol;Acc:HGNC:33627]","synonyms":"NLF1,FAM148A","biotype":"protein_coding","ncbi_id":"145741","summary":null,"start":62066977,"end":62070917,"strand":1,"description":"C2 calcium dependent domain containing 4A [Source:HGNC Symbol;Acc:HGNC:33627]"}, {"versioned_ensembl_gene_id":"ENSG00000216364.1","gene_symbol":"MRPL42P2","gene_name":"mitochondrial ribosomal protein L42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"346116","summary":null,"start":16171606,"end":16172031,"strand":1,"description":"mitochondrial ribosomal protein L42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29711]"}, {"versioned_ensembl_gene_id":"ENSG00000217078.1","gene_symbol":"AL021407.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16163377,"end":16163762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235639.1","gene_symbol":"AC002069.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88512029,"end":88513187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196656.7","gene_symbol":"AC004057.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":113214046,"end":113217170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165140.9","gene_symbol":"FBP1","gene_name":"fructose-bisphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3606]","synonyms":"FBP","biotype":"protein_coding","ncbi_id":"2203","summary":"Fructose-1,6-bisphosphatase 1, a gluconeogenesis regulatory enzyme, catalyzes the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate and inorganic phosphate. Fructose-1,6-diphosphatase deficiency is associated with hypoglycemia and metabolic acidosis. [provided by RefSeq, Jul 2008]","start":94603133,"end":94640249,"strand":-1,"description":"fructose-bisphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3606]"}, {"versioned_ensembl_gene_id":"ENSG00000263612.1","gene_symbol":"AF186192.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144713899,"end":144714845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139352.3","gene_symbol":"ASCL1","gene_name":"achaete-scute family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:738]","synonyms":"ASH1,HASH1,bHLHa46","biotype":"protein_coding","ncbi_id":"429","summary":"This gene encodes a member of the basic helix-loop-helix (BHLH) family of transcription factors. The protein activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. This protein plays a role in the neuronal commitment and differentiation and in the generation of olfactory and autonomic neurons. Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases. [provided by RefSeq, Jul 2008]","start":102957686,"end":102960516,"strand":1,"description":"achaete-scute family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:738]"}, {"versioned_ensembl_gene_id":"ENSG00000151502.10","gene_symbol":"VPS26B","gene_name":"VPS26, retromer complex component B [Source:HGNC Symbol;Acc:HGNC:28119]","synonyms":"Pep8b,MGC10485","biotype":"protein_coding","ncbi_id":"112936","summary":null,"start":134224645,"end":134247792,"strand":1,"description":"VPS26, retromer complex component B [Source:HGNC Symbol;Acc:HGNC:28119]"}, {"versioned_ensembl_gene_id":"ENSG00000224815.3","gene_symbol":"AL691447.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94338347,"end":94338733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225959.1","gene_symbol":"MTND4P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42190]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873189","summary":null,"start":68266319,"end":68266859,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42190]"}, {"versioned_ensembl_gene_id":"ENSG00000176903.4","gene_symbol":"PNMA1","gene_name":"paraneoplastic Ma antigen 1 [Source:HGNC Symbol;Acc:HGNC:9158]","synonyms":"MA1","biotype":"protein_coding","ncbi_id":"9240","summary":"This gene encodes a neuron- and testis-specific protein that is also expressed in some paraneoplastic syndromes affecting the nervous system. Some patients with neurologic disorders develop antibodies against the protein encoded by this gene. The identification of the antineuronal antibodies in the sera of these patients has facilitated the diagnosis of paraneoplastic neurological disorders and the early detection of the associated tumors. [provided by RefSeq, Feb 2014]","start":73711783,"end":73714372,"strand":-1,"description":"paraneoplastic Ma antigen 1 [Source:HGNC Symbol;Acc:HGNC:9158]"}, {"versioned_ensembl_gene_id":"ENSG00000151779.12","gene_symbol":"NBAS","gene_name":"neuroblastoma amplified sequence [Source:HGNC Symbol;Acc:HGNC:15625]","synonyms":"NAG","biotype":"protein_coding","ncbi_id":"51594","summary":"This gene encodes a protein with two leucine zipper domains, a ribosomal protein S14 signature domain and a Sec39 like domain. The protein is thought to be involved in Golgi-to-ER transport. Mutations in this gene are associated with short stature, optic nerve atrophy, and Pelger-Huet anomaly. [provided by RefSeq, Oct 2012]","start":15166909,"end":15561330,"strand":-1,"description":"neuroblastoma amplified sequence [Source:HGNC Symbol;Acc:HGNC:15625]"}, {"versioned_ensembl_gene_id":"ENSG00000225392.1","gene_symbol":"AC016700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70102551,"end":70102862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248486.1","gene_symbol":"LINC02149","gene_name":"long intergenic non-protein coding RNA 2149 [Source:HGNC Symbol;Acc:HGNC:53010]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929454","summary":null,"start":15192139,"end":15266541,"strand":-1,"description":"long intergenic non-protein coding RNA 2149 [Source:HGNC Symbol;Acc:HGNC:53010]"}, {"versioned_ensembl_gene_id":"ENSG00000280349.1","gene_symbol":"AC008133.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":33099969,"end":33100319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079616.12","gene_symbol":"KIF22","gene_name":"kinesin family member 22 [Source:HGNC Symbol;Acc:HGNC:6391]","synonyms":"OBP-2,OBP-1,KNSL4,Kid","biotype":"protein_coding","ncbi_id":"3835","summary":"The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. The C-terminal half of this protein has been shown to bind DNA. Studies with the Xenopus homolog suggests its essential role in metaphase chromosome alignment and maintenance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":29790719,"end":29805385,"strand":1,"description":"kinesin family member 22 [Source:HGNC Symbol;Acc:HGNC:6391]"}, {"versioned_ensembl_gene_id":"ENSG00000163263.6","gene_symbol":"C1orf189","gene_name":"chromosome 1 open reading frame 189 [Source:HGNC Symbol;Acc:HGNC:32305]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388701","summary":null,"start":154199372,"end":154206333,"strand":-1,"description":"chromosome 1 open reading frame 189 [Source:HGNC Symbol;Acc:HGNC:32305]"}, {"versioned_ensembl_gene_id":"ENSG00000279474.1","gene_symbol":"AC125437.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79144752,"end":79146918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232760.1","gene_symbol":"AC103564.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131833783,"end":131836532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153930.11","gene_symbol":"ANKFN1","gene_name":"ankyrin repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26766]","synonyms":"FLJ38335","biotype":"protein_coding","ncbi_id":"162282","summary":null,"start":55882301,"end":56511659,"strand":1,"description":"ankyrin repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26766]"}, {"versioned_ensembl_gene_id":"ENSG00000204767.3","gene_symbol":"FAM196B","gene_name":"family with sequence similarity 196 member B [Source:HGNC Symbol;Acc:HGNC:37271]","synonyms":"C5orf57","biotype":"protein_coding","ncbi_id":"100131897","summary":null,"start":169864264,"end":169980740,"strand":-1,"description":"family with sequence similarity 196 member B [Source:HGNC Symbol;Acc:HGNC:37271]"}, {"versioned_ensembl_gene_id":"ENSG00000101384.11","gene_symbol":"JAG1","gene_name":"jagged 1 [Source:HGNC Symbol;Acc:HGNC:6188]","synonyms":"JAGL1,HJ1,CD339,AWS,AHD,AGS","biotype":"protein_coding","ncbi_id":"182","summary":"The jagged 1 protein encoded by JAG1 is the human homolog of the Drosophilia jagged protein. Human jagged 1 is the ligand for the receptor notch 1, the latter is involved in signaling processes. Mutations that alter the jagged 1 protein cause Alagille syndrome. Jagged 1 signalling through notch 1 has also been shown to play a role in hematopoiesis. [provided by RefSeq, Nov 2019]","start":10637684,"end":10674107,"strand":-1,"description":"jagged 1 [Source:HGNC Symbol;Acc:HGNC:6188]"}, {"versioned_ensembl_gene_id":"ENSG00000254270.1","gene_symbol":"ERHP1","gene_name":"ERH pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507125","summary":null,"start":139534240,"end":139534549,"strand":1,"description":"ERH pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41916]"}, {"versioned_ensembl_gene_id":"ENSG00000250182.3","gene_symbol":"EEF1A1P13","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:3196]","synonyms":"EEF1AL11","biotype":"processed_pseudogene","ncbi_id":"133283","summary":null,"start":14651941,"end":14653329,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:3196]"}, {"versioned_ensembl_gene_id":"ENSG00000224367.6","gene_symbol":"OACYLP","gene_name":"O-acyltransferase like, pseudogene [Source:HGNC Symbol;Acc:HGNC:44362]","synonyms":"ACYL3P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"390858","summary":"This gene is ancient and exists in archaea, bacteria, fungi, worms, flies, and mammals. The gene has been inactivated by mutation and is nonfunctional in humans and chimpanzees. [provided by RefSeq, Oct 2008]","start":58996734,"end":59069338,"strand":1,"description":"O-acyltransferase like, pseudogene [Source:HGNC Symbol;Acc:HGNC:44362]"}, {"versioned_ensembl_gene_id":"ENSG00000215267.8","gene_symbol":"AKR1C7P","gene_name":"aldo-keto reductase family 1 member C7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44681]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"648947","summary":null,"start":5275173,"end":5288470,"strand":-1,"description":"aldo-keto reductase family 1 member C7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44681]"}, {"versioned_ensembl_gene_id":"ENSG00000232659.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31370871,"end":31371297,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000279681.1","gene_symbol":"AC092135.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81617038,"end":81617543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260229.1","gene_symbol":"AC092139.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81476023,"end":81476519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165264.10","gene_symbol":"NDUFB6","gene_name":"NADH:ubiquinone oxidoreductase subunit B6 [Source:HGNC Symbol;Acc:HGNC:7701]","synonyms":"CI,B17","biotype":"protein_coding","ncbi_id":"4712","summary":"The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing occurs at this locus and three transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jan 2011]","start":32552999,"end":32573184,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B6 [Source:HGNC Symbol;Acc:HGNC:7701]"}, {"versioned_ensembl_gene_id":"ENSG00000152217.16","gene_symbol":"SETBP1","gene_name":"SET binding protein 1 [Source:HGNC Symbol;Acc:HGNC:15573]","synonyms":"SEB,KIAA0437","biotype":"protein_coding","ncbi_id":"26040","summary":"This gene encodes a protein which contains a several motifs including a ski homology region and a SET-binding region in addition to three nuclear localization signals. The encoded protein has been shown to bind the SET nuclear oncogene which is involved in DNA replication. Mutations in this gene are associated with Schinzel-Giedion midface retraction syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":44680173,"end":45068510,"strand":1,"description":"SET binding protein 1 [Source:HGNC Symbol;Acc:HGNC:15573]"}, {"versioned_ensembl_gene_id":"ENSG00000235699.2","gene_symbol":"CXorf51B","gene_name":"chromosome X open reading frame 51B [Source:HGNC Symbol;Acc:HGNC:42787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100133053","summary":null,"start":146809784,"end":146810409,"strand":1,"description":"chromosome X open reading frame 51B [Source:HGNC Symbol;Acc:HGNC:42787]"}, {"versioned_ensembl_gene_id":"ENSG00000259255.1","gene_symbol":"AC073941.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46693288,"end":46804844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108924.13","gene_symbol":"HLF","gene_name":"HLF, PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:4977]","synonyms":"MGC33822","biotype":"protein_coding","ncbi_id":"3131","summary":"This gene encodes a member of the proline and acidic-rich (PAR) protein family, a subset of the bZIP transcription factors. The encoded protein forms homodimers or heterodimers with other PAR family members and binds sequence-specific promoter elements to activate transcription. Chromosomal translocations fusing portions of this gene with the E2A gene cause a subset of childhood B-lineage acute lymphoid leukemias. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":55265012,"end":55325065,"strand":1,"description":"HLF, PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:4977]"}, {"versioned_ensembl_gene_id":"ENSG00000232595.1","gene_symbol":"CST2P1","gene_name":"cystatin SA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45042]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101410546","summary":null,"start":23711320,"end":23711406,"strand":-1,"description":"cystatin SA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45042]"}, {"versioned_ensembl_gene_id":"ENSG00000234121.1","gene_symbol":"GPM6BP3","gene_name":"glycoprotein M6B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873787","summary":null,"start":16837522,"end":16837666,"strand":1,"description":"glycoprotein M6B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38783]"}, {"versioned_ensembl_gene_id":"ENSG00000229027.3","gene_symbol":"HSFY1P1","gene_name":"heat shock transcription factor, Y-linked 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1846]","synonyms":"HSFYP1,HSFYL1,CECR8","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"27437","summary":null,"start":16827474,"end":16829335,"strand":1,"description":"heat shock transcription factor, Y-linked 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1846]"}, {"versioned_ensembl_gene_id":"ENSG00000260810.1","gene_symbol":"AL135818.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91258299,"end":91259003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272161.1","gene_symbol":"AL589739.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2326201,"end":2326693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279469.1","gene_symbol":"AC109454.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134394360,"end":134395008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227082.1","gene_symbol":"AC244021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121396754,"end":121463129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261813.2","gene_symbol":"AC015720.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74976240,"end":74976573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260443.1","gene_symbol":"AC127455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87945058,"end":87945202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183397.5","gene_symbol":"C19orf71","gene_name":"chromosome 19 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34496]","synonyms":"LOC100128569","biotype":"protein_coding","ncbi_id":"100128569","summary":null,"start":3539154,"end":3544030,"strand":1,"description":"chromosome 19 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34496]"}, {"versioned_ensembl_gene_id":"ENSG00000005189.19","gene_symbol":"REXO5","gene_name":"RNA exonuclease 5 [Source:HGNC Symbol;Acc:HGNC:24661]","synonyms":"NEF-sp","biotype":"protein_coding","ncbi_id":"81691","summary":null,"start":20806429,"end":20849668,"strand":1,"description":"RNA exonuclease 5 [Source:HGNC Symbol;Acc:HGNC:24661]"}, {"versioned_ensembl_gene_id":"ENSG00000198874.12","gene_symbol":"TYW1","gene_name":"tRNA-yW synthesizing protein 1 homolog [Source:HGNC Symbol;Acc:HGNC:25598]","synonyms":"YPL207W,TYW1A,RSAFD1,MGC60291,MGC23001,FLJ10900","biotype":"protein_coding","ncbi_id":"55253","summary":"Wybutosine (yW) is a hypermodified guanosine found in phenylalanine tRNA adjacent to the anticodon that stabilizes codon-anticodon interactions in the ribosome. In yeast, the homolog of this gene is essential for the synthesis of wybutosine. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":66995173,"end":67239519,"strand":1,"description":"tRNA-yW synthesizing protein 1 homolog [Source:HGNC Symbol;Acc:HGNC:25598]"}, {"versioned_ensembl_gene_id":"ENSG00000066926.10","gene_symbol":"FECH","gene_name":"ferrochelatase [Source:HGNC Symbol;Acc:HGNC:3647]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2235","summary":"The protein encoded by this gene is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome 3.[provided by RefSeq, May 2010]","start":57548283,"end":57586772,"strand":-1,"description":"ferrochelatase [Source:HGNC Symbol;Acc:HGNC:3647]"}, {"versioned_ensembl_gene_id":"ENSG00000186088.15","gene_symbol":"GSAP","gene_name":"gamma-secretase activating protein [Source:HGNC Symbol;Acc:HGNC:28042]","synonyms":"PION,LOC54103","biotype":"protein_coding","ncbi_id":"54103","summary":"Accumulation of neurotoxic amyloid-beta is a major hallmark of Alzheimer disease (AD; MIM 104300). Formation of amyloid-beta is catalyzed by gamma-secretase (see PSEN1; MIM 104311), a protease with numerous substrates. PION, or GSAP, selectively increases amyloid-beta production through a mechanism involving its interaction with both gamma-secretase and its substrate, the amyloid-beta precursor protein (APP; MIM 104760) C-terminal fragment (APP-CTF) (He et al., 2010 [PubMed 20811458]).[supplied by OMIM, Nov 2010]","start":77310751,"end":77416400,"strand":-1,"description":"gamma-secretase activating protein [Source:HGNC Symbol;Acc:HGNC:28042]"}, {"versioned_ensembl_gene_id":"ENSG00000282522.1","gene_symbol":"PKD1P1","gene_name":"polycystin 1, transient receptor potential channel interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30065]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339044","summary":null,"start":16395246,"end":16465697,"strand":1,"description":"polycystin 1, transient receptor potential channel interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30065]"}, {"versioned_ensembl_gene_id":"ENSG00000277390.1","gene_symbol":"APOL5","gene_name":"apolipoprotein L5 [Source:HGNC Symbol;Acc:HGNC:14869]","synonyms":"APOLV","biotype":"protein_coding","ncbi_id":"80831","summary":"This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. [provided by RefSeq, Jul 2008]","start":35717872,"end":35729483,"strand":1,"description":"apolipoprotein L5 [Source:HGNC Symbol;Acc:HGNC:14869]"}, {"versioned_ensembl_gene_id":"ENSG00000281923.1","gene_symbol":"IGHVII-53-1","gene_name":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]","synonyms":"IGHV(II)-53-1","biotype":"IG_V_pseudogene","ncbi_id":"28362","summary":null,"start":106624351,"end":106624605,"strand":-1,"description":"immunoglobulin heavy variable (II)-53-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5685]"}, {"versioned_ensembl_gene_id":"ENSG00000179796.11","gene_symbol":"LRRC3B","gene_name":"leucine rich repeat containing 3B [Source:HGNC Symbol;Acc:HGNC:28105]","synonyms":"LRP15","biotype":"protein_coding","ncbi_id":"116135","summary":"The protein encoded by this gene is a tumor suppressor, with lowered expression levels found in gastric, renal, colorectal, lung, and breast cancer tissues. The promoter of this gene is frequently hypermethylated in these cancer tissues, although the hypermethylation does not appear to be the cause of the reduced expression of this gene. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015]","start":26622806,"end":26710776,"strand":1,"description":"leucine rich repeat containing 3B [Source:HGNC Symbol;Acc:HGNC:28105]"}, {"versioned_ensembl_gene_id":"ENSG00000104904.12","gene_symbol":"OAZ1","gene_name":"ornithine decarboxylase antizyme 1 [Source:HGNC Symbol;Acc:HGNC:8095]","synonyms":"OAZ,MGC138338,AZI","biotype":"protein_coding","ncbi_id":"4946","summary":"The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamine levels. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 1, the first member of the antizyme family, that has broad tissue distribution, and negatively regulates intracellular polyamine levels by binding to and targeting ODC for degradation, as well as inhibiting polyamine uptake. Antizyme 1 mRNA contains two potential in-frame AUGs; and studies in rat suggest that alternative use of the two translation initiation sites results in N-terminally distinct protein isoforms with different subcellular localization. Alternatively spliced transcript variants have also been noted for this gene. [provided by RefSeq, Dec 2014]","start":2269509,"end":2273490,"strand":1,"description":"ornithine decarboxylase antizyme 1 [Source:HGNC Symbol;Acc:HGNC:8095]"}, {"versioned_ensembl_gene_id":"ENSG00000272595.2","gene_symbol":"AC092028.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5103719,"end":5120245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204658.5","gene_symbol":"CST9LP2","gene_name":"cystatin 9-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44337]","synonyms":"CTES7D","biotype":"unprocessed_pseudogene","ncbi_id":"106480788","summary":null,"start":23583645,"end":23586510,"strand":1,"description":"cystatin 9-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44337]"}, {"versioned_ensembl_gene_id":"ENSG00000178922.16","gene_symbol":"HYI","gene_name":"hydroxypyruvate isomerase (putative) [Source:HGNC Symbol;Acc:HGNC:26948]","synonyms":"HT036","biotype":"protein_coding","ncbi_id":"81888","summary":"This gene encodes a putative hydroxypyruvate isomerase, which likely catalyzes the conversion of hydroxypyruvate to 2-hydroxy-3-oxopropanoate, and may be involved in carbohydrate transport and metabolism. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":43451003,"end":43453989,"strand":-1,"description":"hydroxypyruvate isomerase (putative) [Source:HGNC Symbol;Acc:HGNC:26948]"}, {"versioned_ensembl_gene_id":"ENSG00000225854.2","gene_symbol":"AL451139.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26326688,"end":26327033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256650.1","gene_symbol":"RERG-IT1","gene_name":"RERG intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39991]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874290","summary":null,"start":15112363,"end":15114698,"strand":-1,"description":"RERG intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39991]"}, {"versioned_ensembl_gene_id":"ENSG00000232922.1","gene_symbol":"MTND6P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51982]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107063611","summary":null,"start":112373733,"end":112374250,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51982]"}, {"versioned_ensembl_gene_id":"ENSG00000255660.1","gene_symbol":"RERG-AS1","gene_name":"RERG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39990]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100873980","summary":null,"start":15151923,"end":15155283,"strand":1,"description":"RERG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39990]"}, {"versioned_ensembl_gene_id":"ENSG00000168813.16","gene_symbol":"ZNF507","gene_name":"zinc finger protein 507 [Source:HGNC Symbol;Acc:HGNC:23783]","synonyms":"KIAA1084","biotype":"protein_coding","ncbi_id":"22847","summary":null,"start":32345594,"end":32387667,"strand":1,"description":"zinc finger protein 507 [Source:HGNC Symbol;Acc:HGNC:23783]"}, {"versioned_ensembl_gene_id":"ENSG00000248564.1","gene_symbol":"AC079140.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":338097,"end":338583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172244.8","gene_symbol":"C5orf34","gene_name":"chromosome 5 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:24738]","synonyms":"FLJ32363","biotype":"protein_coding","ncbi_id":"375444","summary":null,"start":43486701,"end":43515145,"strand":-1,"description":"chromosome 5 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:24738]"}, {"versioned_ensembl_gene_id":"ENSG00000128617.2","gene_symbol":"OPN1SW","gene_name":"opsin 1, short wave sensitive [Source:HGNC Symbol;Acc:HGNC:1012]","synonyms":"CBT,BOP,BCP","biotype":"protein_coding","ncbi_id":"611","summary":"This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]","start":128772491,"end":128775790,"strand":-1,"description":"opsin 1, short wave sensitive [Source:HGNC Symbol;Acc:HGNC:1012]"}, {"versioned_ensembl_gene_id":"ENSG00000189002.10","gene_symbol":"PROS2P","gene_name":"protein S (beta) pseudogene [Source:HGNC Symbol;Acc:HGNC:9458]","synonyms":"PROSP,PROS2","biotype":"unprocessed_pseudogene","ncbi_id":"5628","summary":null,"start":90202316,"end":90257415,"strand":-1,"description":"protein S (beta) pseudogene [Source:HGNC Symbol;Acc:HGNC:9458]"}, {"versioned_ensembl_gene_id":"ENSG00000116030.16","gene_symbol":"SUMO1","gene_name":"small ubiquitin-like modifier 1 [Source:HGNC Symbol;Acc:HGNC:12502]","synonyms":"PIC1,OFC10,GMP1,UBL1,SUMO-1,SMT3H3,SMT3C","biotype":"protein_coding","ncbi_id":"7341","summary":"This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last four amino acids of the carboxy-terminus have been cleaved off. Several pseudogenes have been reported for this gene. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008]","start":202206180,"end":202238608,"strand":-1,"description":"small ubiquitin-like modifier 1 [Source:HGNC Symbol;Acc:HGNC:12502]"}, {"versioned_ensembl_gene_id":"ENSG00000231515.1","gene_symbol":"AC006003.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":157739010,"end":157740456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258780.1","gene_symbol":"BMS1P15","gene_name":"BMS1, ribosome biogenesis factor pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49160]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642311","summary":null,"start":20153776,"end":20160826,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49160]"}, {"versioned_ensembl_gene_id":"ENSG00000225649.5","gene_symbol":"AC064875.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":12966784,"end":13007013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077235.17","gene_symbol":"GTF3C1","gene_name":"general transcription factor IIIC subunit 1 [Source:HGNC Symbol;Acc:HGNC:4664]","synonyms":"TFIIIC220","biotype":"protein_coding","ncbi_id":"2975","summary":null,"start":27459555,"end":27549913,"strand":-1,"description":"general transcription factor IIIC subunit 1 [Source:HGNC Symbol;Acc:HGNC:4664]"}, {"versioned_ensembl_gene_id":"ENSG00000258695.2","gene_symbol":"AC005225.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73522878,"end":73530610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260498.5","gene_symbol":"AC126696.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87773488,"end":87779374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241394.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32926550,"end":32931062,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000243438.1","gene_symbol":"LARP1BP2","gene_name":"La ribonucleoprotein domain family member 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44084]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479034","summary":null,"start":106315225,"end":106315743,"strand":1,"description":"La ribonucleoprotein domain family member 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44084]"}, {"versioned_ensembl_gene_id":"ENSG00000237871.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32874341,"end":32874415,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000240616.1","gene_symbol":"RPS6P25","gene_name":"ribosomal protein S6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35948]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729389","summary":null,"start":12894133,"end":12894880,"strand":1,"description":"ribosomal protein S6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35948]"}, {"versioned_ensembl_gene_id":"ENSG00000227149.1","gene_symbol":"MTCO1P44","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52109]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075226","summary":null,"start":140216997,"end":140217239,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52109]"}, {"versioned_ensembl_gene_id":"ENSG00000105607.12","gene_symbol":"GCDH","gene_name":"glutaryl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4189]","synonyms":"ACAD5","biotype":"protein_coding","ncbi_id":"2639","summary":"The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12. [provided by RefSeq, Mar 2013]","start":12891026,"end":12914207,"strand":1,"description":"glutaryl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4189]"}, {"versioned_ensembl_gene_id":"ENSG00000237531.6","gene_symbol":"AL672277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":990221,"end":994365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217680.1","gene_symbol":"UBE2V1P15","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52414]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288170","summary":null,"start":75465123,"end":75465570,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52414]"}, {"versioned_ensembl_gene_id":"ENSG00000232992.2","gene_symbol":"AHCYP4","gene_name":"adenosylhomocysteinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44996]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"129560","summary":null,"start":138901433,"end":138902747,"strand":-1,"description":"adenosylhomocysteinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44996]"}, {"versioned_ensembl_gene_id":"ENSG00000183726.10","gene_symbol":"TMEM50A","gene_name":"transmembrane protein 50A [Source:HGNC Symbol;Acc:HGNC:30590]","synonyms":"SMP1","biotype":"protein_coding","ncbi_id":"23585","summary":"This gene is located in the RH gene locus, between the RHD and RHCE genes. The function of its protein product is unknown; however, its sequence has potential transmembrane domains suggesting that it may be an integral membrane protein. Its position between the RH genes suggests that polymorphisms in this gene may be tightly linked to RH haplotypes and may contribute to selective pressure for or against certain RH haplotypes. [provided by RefSeq, Jul 2008]","start":25337917,"end":25362361,"strand":1,"description":"transmembrane protein 50A [Source:HGNC Symbol;Acc:HGNC:30590]"}, {"versioned_ensembl_gene_id":"ENSG00000233396.7","gene_symbol":"LINC01719","gene_name":"long intergenic non-protein coding RNA 1719 [Source:HGNC Symbol;Acc:HGNC:52506]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928979","summary":null,"start":146052566,"end":146061948,"strand":1,"description":"long intergenic non-protein coding RNA 1719 [Source:HGNC Symbol;Acc:HGNC:52506]"}, {"versioned_ensembl_gene_id":"ENSG00000259060.7","gene_symbol":"AL163195.3","gene_name":"probable ribonuclease 11 precursor [Source:RefSeq peptide;Acc:NP_660293]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":20582892,"end":20609795,"strand":-1,"description":"probable ribonuclease 11 precursor [Source:RefSeq peptide;Acc:NP_660293]"}, {"versioned_ensembl_gene_id":"ENSG00000257150.3","gene_symbol":"PGAM1P5","gene_name":"phosphoglycerate mutase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42452]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100132594","summary":null,"start":95551582,"end":95673999,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42452]"}, {"versioned_ensembl_gene_id":"ENSG00000260201.2","gene_symbol":"AC141273.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20580999,"end":20586640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271532.1","gene_symbol":"BBIP1P1","gene_name":"BBSome interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105373509","summary":null,"start":101068378,"end":101068656,"strand":1,"description":"BBSome interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52781]"}, {"versioned_ensembl_gene_id":"ENSG00000267586.6","gene_symbol":"LINC00907","gene_name":"long intergenic non-protein coding RNA 907 [Source:HGNC Symbol;Acc:HGNC:44327]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284260","summary":null,"start":42159283,"end":42691422,"strand":1,"description":"long intergenic non-protein coding RNA 907 [Source:HGNC Symbol;Acc:HGNC:44327]"}, {"versioned_ensembl_gene_id":"ENSG00000101224.17","gene_symbol":"CDC25B","gene_name":"cell division cycle 25B [Source:HGNC Symbol;Acc:HGNC:1726]","synonyms":null,"biotype":"protein_coding","ncbi_id":"994","summary":"CDC25B is a member of the CDC25 family of phosphatases. CDC25B activates the cyclin dependent kinase CDC2 by removing two phosphate groups and it is required for entry into mitosis. CDC25B shuttles between the nucleus and the cytoplasm due to nuclear localization and nuclear export signals. The protein is nuclear in the M and G1 phases of the cell cycle and moves to the cytoplasm during S and G2. CDC25B has oncogenic properties, although its role in tumor formation has not been determined. Multiple transcript variants for this gene exist. [provided by RefSeq, Jul 2008]","start":3786772,"end":3806121,"strand":1,"description":"cell division cycle 25B [Source:HGNC Symbol;Acc:HGNC:1726]"}, {"versioned_ensembl_gene_id":"ENSG00000255949.1","gene_symbol":"AP003419.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67431367,"end":67435399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271547.1","gene_symbol":"AC117498.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48800576,"end":48801086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226160.1","gene_symbol":"AC137499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16405330,"end":16405417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225293.1","gene_symbol":"ABCD1P4","gene_name":"ATP binding cassette subfamily D member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:65]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"26957","summary":null,"start":16387694,"end":16390887,"strand":1,"description":"ATP binding cassette subfamily D member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:65]"}, {"versioned_ensembl_gene_id":"ENSG00000215567.5","gene_symbol":"AC138701.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19878555,"end":19887814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000026297.15","gene_symbol":"RNASET2","gene_name":"ribonuclease T2 [Source:HGNC Symbol;Acc:HGNC:21686]","synonyms":"RNASE6PL,FLJ10907,bA514O12.3","biotype":"protein_coding","ncbi_id":"8635","summary":"This ribonuclease gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular ribonucleases. It is a single copy gene that maps to 6q27, a region associated with human malignancies and chromosomal rearrangement. [provided by RefSeq, Jul 2008]","start":166929504,"end":166957191,"strand":-1,"description":"ribonuclease T2 [Source:HGNC Symbol;Acc:HGNC:21686]"}, {"versioned_ensembl_gene_id":"ENSG00000253861.1","gene_symbol":"SLC2A3P1","gene_name":"solute carrier family 2 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11008]","synonyms":"SLC2A3P,GLUT6,GLUT3P1","biotype":"processed_pseudogene","ncbi_id":"100128062","summary":null,"start":168552277,"end":168553727,"strand":-1,"description":"solute carrier family 2 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11008]"}, {"versioned_ensembl_gene_id":"ENSG00000245958.6","gene_symbol":"AC093752.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":119454791,"end":119552025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248302.3","gene_symbol":"BNIP3P41","gene_name":"BCL2 interacting protein 3 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:49721]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"101059988","summary":null,"start":49096,"end":50124,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:49721]"}, {"versioned_ensembl_gene_id":"ENSG00000284638.1","gene_symbol":"AC005551.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3482804,"end":3483446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279785.1","gene_symbol":"AC008267.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":66474556,"end":66475749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255238.1","gene_symbol":"RFPL4AP1","gene_name":"ret finger protein like 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45138]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646663","summary":null,"start":55777553,"end":55778900,"strand":1,"description":"ret finger protein like 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45138]"}, {"versioned_ensembl_gene_id":"ENSG00000232335.1","gene_symbol":"AL354864.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35739389,"end":35743576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087053.18","gene_symbol":"MTMR2","gene_name":"myotubularin related protein 2 [Source:HGNC Symbol;Acc:HGNC:7450]","synonyms":"KIAA1073,CMT4B","biotype":"protein_coding","ncbi_id":"8898","summary":"This gene is a member of the myotubularin family of phosphoinositide lipid phosphatases. The encoded protein possesses phosphatase activity towards phosphatidylinositol-3-phosphate and phosphatidylinositol-3,5-bisphosphate. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4B, an autosomal recessive demyelinating neuropathy. Alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":95832882,"end":95925315,"strand":-1,"description":"myotubularin related protein 2 [Source:HGNC Symbol;Acc:HGNC:7450]"}, {"versioned_ensembl_gene_id":"ENSG00000160685.13","gene_symbol":"ZBTB7B","gene_name":"zinc finger and BTB domain containing 7B [Source:HGNC Symbol;Acc:HGNC:18668]","synonyms":"ZNF857B,ZFP67,ZBTB15,hcKrox,c-Krox","biotype":"protein_coding","ncbi_id":"51043","summary":"This gene encodes a zinc finger-containing transcription factor that acts as a key regulator of lineage commitment of immature T-cell precursors. It is necessary and sufficient for commitment of CD4 lineage, while its absence causes CD8 commitment. It also functions as a transcriptional repressor of type I collagen genes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":155002630,"end":155018522,"strand":1,"description":"zinc finger and BTB domain containing 7B [Source:HGNC Symbol;Acc:HGNC:18668]"}, {"versioned_ensembl_gene_id":"ENSG00000232915.1","gene_symbol":"AC097721.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138412066,"end":138413318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282332.1","gene_symbol":"AC244489.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16375283,"end":16377390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244561.1","gene_symbol":"AC092905.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109396616,"end":109397870,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280057.1","gene_symbol":"AL022069.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":166388136,"end":166389920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244306.10","gene_symbol":"DUXAP10","gene_name":"double homeobox A pseudogene 10 [Source:NCBI gene;Acc:503639]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"503639","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":19284653,"end":19337730,"strand":-1,"description":"double homeobox A pseudogene 10 [Source:NCBI gene;Acc:503639]"}, {"versioned_ensembl_gene_id":"ENSG00000183709.7","gene_symbol":"IFNL2","gene_name":"interferon lambda 2 [Source:HGNC Symbol;Acc:HGNC:18364]","synonyms":"IL28A,IL-28A","biotype":"protein_coding","ncbi_id":"282616","summary":"This gene encodes a cytokine distantly related to type I interferons and the IL-10 family. This gene, interleukin 28B (IL28B), and interleukin 29 (IL29) are three closely related cytokine genes that form a cytokine gene cluster on a chromosomal region mapped to 19q13. Expression of the cytokines encoded by the three genes can be induced by viral infection. All three cytokines have been shown to interact with a heterodimeric class II cytokine receptor that consists of interleukin 10 receptor, beta (IL10RB) and interleukin 28 receptor, alpha (IL28RA). [provided by RefSeq, Jul 2008]","start":39268514,"end":39270092,"strand":1,"description":"interferon lambda 2 [Source:HGNC Symbol;Acc:HGNC:18364]"}, {"versioned_ensembl_gene_id":"ENSG00000278530.4","gene_symbol":"CHMP1B2P","gene_name":"charged multivesicular body protein 1B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49380]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"101060146","summary":null,"start":80228489,"end":80335364,"strand":-1,"description":"charged multivesicular body protein 1B2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49380]"}, {"versioned_ensembl_gene_id":"ENSG00000142794.18","gene_symbol":"NBPF3","gene_name":"NBPF member 3 [Source:HGNC Symbol;Acc:HGNC:25076]","synonyms":"AE2","biotype":"protein_coding","ncbi_id":"84224","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. DUF1220 copy number variations in human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Feb 2013]","start":21440128,"end":21485005,"strand":1,"description":"NBPF member 3 [Source:HGNC Symbol;Acc:HGNC:25076]"}, {"versioned_ensembl_gene_id":"ENSG00000213926.3","gene_symbol":"MSRB1P1","gene_name":"methionine sulfoxide reductase B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43985]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441849","summary":null,"start":39254916,"end":39255269,"strand":-1,"description":"methionine sulfoxide reductase B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43985]"}, {"versioned_ensembl_gene_id":"ENSG00000225890.10","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32780908,"end":32803273,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000274541.1","gene_symbol":"AL121955.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11015586,"end":11015888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000040531.14","gene_symbol":"CTNS","gene_name":"cystinosin, lysosomal cystine transporter [Source:HGNC Symbol;Acc:HGNC:2518]","synonyms":"PQLC4,CTNS-LSB","biotype":"protein_coding","ncbi_id":"1497","summary":"This gene encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes. Its activity is driven by the H+ electrochemical gradient of the lysosomal membrane. Mutations in this gene cause cystinosis, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":3636468,"end":3661542,"strand":1,"description":"cystinosin, lysosomal cystine transporter [Source:HGNC Symbol;Acc:HGNC:2518]"}, {"versioned_ensembl_gene_id":"ENSG00000280534.2","gene_symbol":"LINC01347","gene_name":"long intergenic non-protein coding RNA 1347 [Source:HGNC Symbol;Acc:HGNC:50566]","synonyms":null,"biotype":"lincRNA","ncbi_id":"731275","summary":null,"start":243029512,"end":243047869,"strand":-1,"description":"long intergenic non-protein coding RNA 1347 [Source:HGNC Symbol;Acc:HGNC:50566]"}, {"versioned_ensembl_gene_id":"ENSG00000255438.2","gene_symbol":"AL354813.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47677901,"end":47686297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158092.6","gene_symbol":"NCK1","gene_name":"NCK adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:7664]","synonyms":"NCKalpha,NCK","biotype":"protein_coding","ncbi_id":"4690","summary":"The protein encoded by this gene is one of the signaling and transforming proteins containing Src homology 2 and 3 (SH2 and SH3) domains. It is located in the cytoplasm and is an adaptor protein involved in transducing signals from receptor tyrosine kinases to downstream signal recipients such as RAS. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Jun 2010]","start":136862208,"end":136949823,"strand":1,"description":"NCK adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:7664]"}, {"versioned_ensembl_gene_id":"ENSG00000078596.10","gene_symbol":"ITM2A","gene_name":"integral membrane protein 2A [Source:HGNC Symbol;Acc:HGNC:6173]","synonyms":"E25A,BRICD2A","biotype":"protein_coding","ncbi_id":"9452","summary":"This gene encodes a type II membrane protein that belongs to the ITM2 family. Studies in mouse suggest that it may be involved in osteo- and chondrogenic differentiation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":79360384,"end":79367667,"strand":-1,"description":"integral membrane protein 2A [Source:HGNC Symbol;Acc:HGNC:6173]"}, {"versioned_ensembl_gene_id":"ENSG00000278208.1","gene_symbol":"AC007368.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126364076,"end":126364938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276488.1","gene_symbol":"AC008735.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55612490,"end":55613097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277540.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54837484,"end":54858960,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000147138.1","gene_symbol":"GPR174","gene_name":"G protein-coupled receptor 174 [Source:HGNC Symbol;Acc:HGNC:30245]","synonyms":"FKSG79","biotype":"protein_coding","ncbi_id":"84636","summary":"This gene encodes a protein belonging to the G protein-coupled receptor superfamily. These proteins are characterized by the presence of seven alpha-helical transmembrane domains, and they activate or interact with various endogenous or exogenous ligands, including neurotransmitters, hormones, and odorant and taste substances. This family member is classified as an orphan receptor because the cognate ligand has not been identified. [provided by RefSeq, Sep 2011]","start":79170972,"end":79172229,"strand":1,"description":"G protein-coupled receptor 174 [Source:HGNC Symbol;Acc:HGNC:30245]"}, {"versioned_ensembl_gene_id":"ENSG00000232168.2","gene_symbol":"P2RY10P2","gene_name":"purinergic receptor P2Y10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"449518","summary":null,"start":79084936,"end":79085848,"strand":1,"description":"purinergic receptor P2Y10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32924]"}, {"versioned_ensembl_gene_id":"ENSG00000238084.4","gene_symbol":"AL031284.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25398721,"end":25399198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253978.1","gene_symbol":"CTB-178M22.2","gene_name":"uncharacterized LOC101927862 [Source:NCBI gene;Acc:101927862]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927862","summary":null,"start":168229583,"end":168232357,"strand":-1,"description":"uncharacterized LOC101927862 [Source:NCBI gene;Acc:101927862]"}, {"versioned_ensembl_gene_id":"ENSG00000106399.11","gene_symbol":"RPA3","gene_name":"replication protein A3 [Source:HGNC Symbol;Acc:HGNC:10291]","synonyms":"REPA3","biotype":"protein_coding","ncbi_id":"6119","summary":null,"start":7636518,"end":7718607,"strand":-1,"description":"replication protein A3 [Source:HGNC Symbol;Acc:HGNC:10291]"}, {"versioned_ensembl_gene_id":"ENSG00000261604.1","gene_symbol":"AC114947.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43287601,"end":43290839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109084.13","gene_symbol":"TMEM97","gene_name":"transmembrane protein 97 [Source:HGNC Symbol;Acc:HGNC:28106]","synonyms":"MAC30","biotype":"protein_coding","ncbi_id":"27346","summary":"TMEM97 is a conserved integral membrane protein that plays a role in controlling cellular cholesterol levels (Bartz et al., 2009 [PubMed 19583955]).[supplied by OMIM, Aug 2009]","start":28319095,"end":28328685,"strand":1,"description":"transmembrane protein 97 [Source:HGNC Symbol;Acc:HGNC:28106]"}, {"versioned_ensembl_gene_id":"ENSG00000274365.1","gene_symbol":"AC013412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6789153,"end":6789344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206491.12","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"CAT56,Em:AB023052.2,Em:AB014077.1","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30546378,"end":30553215,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000189252.4","gene_symbol":"SPANXN3","gene_name":"SPANX family member N3 [Source:HGNC Symbol;Acc:HGNC:33176]","synonyms":"SPANX-N3,CT11.8","biotype":"protein_coding","ncbi_id":"139067","summary":null,"start":143508735,"end":143517475,"strand":-1,"description":"SPANX family member N3 [Source:HGNC Symbol;Acc:HGNC:33176]"}, {"versioned_ensembl_gene_id":"ENSG00000260388.2","gene_symbol":"LINC00562","gene_name":"long intergenic non-protein coding RNA 562 [Source:HGNC Symbol;Acc:HGNC:43706]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861549","summary":null,"start":47930153,"end":47932622,"strand":-1,"description":"long intergenic non-protein coding RNA 562 [Source:HGNC Symbol;Acc:HGNC:43706]"}, {"versioned_ensembl_gene_id":"ENSG00000224835.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31648554,"end":31650946,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000182636.5","gene_symbol":"NDN","gene_name":"necdin, MAGE family member [Source:HGNC Symbol;Acc:HGNC:7675]","synonyms":"PWCR,HsT16328","biotype":"protein_coding","ncbi_id":"4692","summary":"This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]","start":23685400,"end":23687330,"strand":-1,"description":"necdin, MAGE family member [Source:HGNC Symbol;Acc:HGNC:7675]"}, {"versioned_ensembl_gene_id":"ENSG00000115355.15","gene_symbol":"CCDC88A","gene_name":"coiled-coil domain containing 88A [Source:HGNC Symbol;Acc:HGNC:25523]","synonyms":"KIAA1212,HkRP1,GRDN,GIV,FLJ10392,APE","biotype":"protein_coding","ncbi_id":"55704","summary":"This gene encodes a member of the Girdin family of coiled-coil domain containing proteins. The encoded protein is an actin-binding protein that is activated by the serine/threonine kinase Akt and plays a role in cytoskeleton remodeling and cell migration. The encoded protein also enhances Akt signaling by mediating phosphoinositide 3-kinase (PI3K)-dependent activation of Akt by growth factor receptor tyrosine kinases and G protein-coupled receptors. Increased expression of this gene and phosphorylation of the encoded protein may play a role in cancer metastasis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55287842,"end":55419921,"strand":-1,"description":"coiled-coil domain containing 88A [Source:HGNC Symbol;Acc:HGNC:25523]"}, {"versioned_ensembl_gene_id":"ENSG00000230009.1","gene_symbol":"MTCO2P3","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39576]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873203","summary":null,"start":57204379,"end":57204799,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39576]"}, {"versioned_ensembl_gene_id":"ENSG00000282267.1","gene_symbol":"IGHV7-27","gene_name":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28383","summary":null,"start":106318594,"end":106319007,"strand":-1,"description":"immunoglobulin heavy variable 7-27 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5663]"}, {"versioned_ensembl_gene_id":"ENSG00000198963.10","gene_symbol":"RORB","gene_name":"RAR related orphan receptor B [Source:HGNC Symbol;Acc:HGNC:10259]","synonyms":"RZRB,ROR-BETA,NR1F2","biotype":"protein_coding","ncbi_id":"6096","summary":"The protein encoded by this gene is a member of the NR1 subfamily of nuclear hormone receptors. It is a DNA-binding protein that can bind as a monomer or as a homodimer to hormone response elements upstream of several genes to enhance the expression of those genes. The encoded protein has been shown to interact with NM23-2, a nucleoside diphosphate kinase involved in organogenesis and differentiation, and to help regulate the expression of some genes involved in circadian rhythm. [provided by RefSeq, Feb 2014]","start":74497365,"end":74693177,"strand":1,"description":"RAR related orphan receptor B [Source:HGNC Symbol;Acc:HGNC:10259]"}, {"versioned_ensembl_gene_id":"ENSG00000275013.4","gene_symbol":"PRAME","gene_name":"preferentially expressed antigen in melanoma [Source:HGNC Symbol;Acc:HGNC:9336]","synonyms":"MAPE,CT130","biotype":"protein_coding","ncbi_id":"23532","summary":"This gene encodes an antigen that is preferentially expressed in human melanomas and that is recognized by cytolytic T lymphocytes. It is not expressed in normal tissues, except testis. The encoded protein acts as a repressor of retinoic acid receptor, and likely confers a growth advantage to cancer cells via this function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":22556806,"end":22568466,"strand":-1,"description":"preferentially expressed antigen in melanoma [Source:HGNC Symbol;Acc:HGNC:9336]"}, {"versioned_ensembl_gene_id":"ENSG00000186543.7","gene_symbol":"CROCCP5","gene_name":"ciliary rootlet coiled-coil, rootletin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43865]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421114","summary":null,"start":21434318,"end":21437558,"strand":1,"description":"ciliary rootlet coiled-coil, rootletin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43865]"}, {"versioned_ensembl_gene_id":"ENSG00000163545.8","gene_symbol":"NUAK2","gene_name":"NUAK family kinase 2 [Source:HGNC Symbol;Acc:HGNC:29558]","synonyms":"SNARK,FLJ90349","biotype":"protein_coding","ncbi_id":"81788","summary":null,"start":205302059,"end":205321791,"strand":-1,"description":"NUAK family kinase 2 [Source:HGNC Symbol;Acc:HGNC:29558]"}, {"versioned_ensembl_gene_id":"ENSG00000231672.6","gene_symbol":"DIRC3","gene_name":"disrupted in renal carcinoma 3 [Source:HGNC Symbol;Acc:HGNC:17805]","synonyms":"FLJ14199","biotype":"protein_coding","ncbi_id":"729582","summary":null,"start":217284019,"end":217756593,"strand":-1,"description":"disrupted in renal carcinoma 3 [Source:HGNC Symbol;Acc:HGNC:17805]"}, {"versioned_ensembl_gene_id":"ENSG00000234381.1","gene_symbol":"MED15P7","gene_name":"mediator complex subunit 15 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48656]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996466","summary":null,"start":15635180,"end":15644330,"strand":-1,"description":"mediator complex subunit 15 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48656]"}, {"versioned_ensembl_gene_id":"ENSG00000236009.1","gene_symbol":"AL592309.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21415898,"end":21417492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228823.1","gene_symbol":"AL592309.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21411460,"end":21413293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201347.1","gene_symbol":"RNA5SP69","gene_name":"RNA, 5S ribosomal pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:42846]","synonyms":"RN5S69","biotype":"rRNA","ncbi_id":"100873304","summary":null,"start":178560913,"end":178561029,"strand":1,"description":"RNA, 5S ribosomal pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:42846]"}, {"versioned_ensembl_gene_id":"ENSG00000258227.6","gene_symbol":"CLEC5A","gene_name":"C-type lectin domain containing 5A [Source:HGNC Symbol;Acc:HGNC:2054]","synonyms":"MDL-1,CLECSF5","biotype":"protein_coding","ncbi_id":"23601","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type II transmembrane protein interacts with dnax-activation protein 12 and may play a role in cell activation. Alternative splice variants have been described but their full-length sequence has not been determined. [provided by RefSeq, Jul 2008]","start":141927357,"end":141947007,"strand":-1,"description":"C-type lectin domain containing 5A [Source:HGNC Symbol;Acc:HGNC:2054]"}, {"versioned_ensembl_gene_id":"ENSG00000249262.2","gene_symbol":"AC112250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87410644,"end":87411388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274369.1","gene_symbol":"GRAMD4P4","gene_name":"GRAM domain containing 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480248","summary":null,"start":19026521,"end":19028189,"strand":-1,"description":"GRAM domain containing 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49139]"}, {"versioned_ensembl_gene_id":"ENSG00000009335.17","gene_symbol":"UBE3C","gene_name":"ubiquitin protein ligase E3C [Source:HGNC Symbol;Acc:HGNC:16803]","synonyms":"KIAA10,KIAA0010","biotype":"protein_coding","ncbi_id":"9690","summary":null,"start":157138913,"end":157269372,"strand":1,"description":"ubiquitin protein ligase E3C [Source:HGNC Symbol;Acc:HGNC:16803]"}, {"versioned_ensembl_gene_id":"ENSG00000233754.2","gene_symbol":"AP001628.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42781074,"end":42782229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234118.1","gene_symbol":"RPL13AP6","gene_name":"ribosomal protein L13a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23737]","synonyms":"bA348N5.5","biotype":"processed_pseudogene","ncbi_id":"644511","summary":null,"start":110936622,"end":110937233,"strand":-1,"description":"ribosomal protein L13a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23737]"}, {"versioned_ensembl_gene_id":"ENSG00000103035.10","gene_symbol":"PSMD7","gene_name":"proteasome 26S subunit, non-ATPase 7 [Source:HGNC Symbol;Acc:HGNC:9565]","synonyms":"S12,Rpn8,P40,MOV34","biotype":"protein_coding","ncbi_id":"5713","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]","start":74296775,"end":74306288,"strand":1,"description":"proteasome 26S subunit, non-ATPase 7 [Source:HGNC Symbol;Acc:HGNC:9565]"}, {"versioned_ensembl_gene_id":"ENSG00000227425.1","gene_symbol":"MRPS21P2","gene_name":"mitochondrial ribosomal protein S21 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359766","summary":null,"start":157861197,"end":157861460,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29749]"}, {"versioned_ensembl_gene_id":"ENSG00000171763.18","gene_symbol":"SPATA5L1","gene_name":"spermatogenesis associated 5 like 1 [Source:HGNC Symbol;Acc:HGNC:28762]","synonyms":"MGC5347,FLJ12286","biotype":"protein_coding","ncbi_id":"79029","summary":null,"start":45402331,"end":45421419,"strand":1,"description":"spermatogenesis associated 5 like 1 [Source:HGNC Symbol;Acc:HGNC:28762]"}, {"versioned_ensembl_gene_id":"ENSG00000122882.10","gene_symbol":"ECD","gene_name":"ecdysoneless cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:17029]","synonyms":"hSGT1,GCR2","biotype":"protein_coding","ncbi_id":"11319","summary":null,"start":73130155,"end":73169055,"strand":-1,"description":"ecdysoneless cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:17029]"}, {"versioned_ensembl_gene_id":"ENSG00000217004.1","gene_symbol":"Z97832.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35279177,"end":35279819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159650.8","gene_symbol":"UROC1","gene_name":"urocanate hydratase 1 [Source:HGNC Symbol;Acc:HGNC:26444]","synonyms":"HMFN0320,FLJ31300","biotype":"protein_coding","ncbi_id":"131669","summary":"This gene encodes an enzyme involved in the second step of histidine catabolism, metabolizing urocanic acid to formiminoglutamic acid. Deficiency of this enzyme results in urocanic aciduria, and is an apparent cause of mental retardation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2021]","start":126481281,"end":126517773,"strand":-1,"description":"urocanate hydratase 1 [Source:HGNC Symbol;Acc:HGNC:26444]"}, {"versioned_ensembl_gene_id":"ENSG00000242661.1","gene_symbol":"RPS3AP43","gene_name":"ribosomal protein S3a pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727970","summary":null,"start":8359054,"end":8359834,"strand":-1,"description":"ribosomal protein S3a pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36684]"}, {"versioned_ensembl_gene_id":"ENSG00000212124.2","gene_symbol":"TAS2R19","gene_name":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]","synonyms":"TAS2R23,T2R23,T2R19,TAS2R48","biotype":"protein_coding","ncbi_id":"259294","summary":null,"start":11021619,"end":11022620,"strand":-1,"description":"taste 2 receptor member 19 [Source:HGNC Symbol;Acc:HGNC:19108]"}, {"versioned_ensembl_gene_id":"ENSG00000164654.15","gene_symbol":"MIOS","gene_name":"meiosis regulator for oocyte development [Source:HGNC Symbol;Acc:HGNC:21905]","synonyms":"FLJ20323,Sea4,MIO","biotype":"protein_coding","ncbi_id":"54468","summary":null,"start":7566872,"end":7608929,"strand":1,"description":"meiosis regulator for oocyte development [Source:HGNC Symbol;Acc:HGNC:21905]"}, {"versioned_ensembl_gene_id":"ENSG00000237930.1","gene_symbol":"AC007563.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":216785774,"end":216786144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236354.1","gene_symbol":"LINC00437","gene_name":"long intergenic non-protein coding RNA 437 [Source:HGNC Symbol;Acc:HGNC:42772]","synonyms":"TCONS_00021639","biotype":"lincRNA","ncbi_id":"101929121","summary":null,"start":38533343,"end":38545299,"strand":-1,"description":"long intergenic non-protein coding RNA 437 [Source:HGNC Symbol;Acc:HGNC:42772]"}, {"versioned_ensembl_gene_id":"ENSG00000282684.1","gene_symbol":"ZC3H3","gene_name":"zinc finger CCCH-type containing 3 [Source:HGNC Symbol;Acc:HGNC:28972]","synonyms":"KIAA0150,ZC3HDC3","biotype":"protein_coding","ncbi_id":"23144","summary":null,"start":143536257,"end":143541453,"strand":-1,"description":"zinc finger CCCH-type containing 3 [Source:HGNC Symbol;Acc:HGNC:28972]"}, {"versioned_ensembl_gene_id":"ENSG00000244184.1","gene_symbol":"AC091153.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4704230,"end":4705529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235085.3","gene_symbol":"AC091153.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4673830,"end":4696831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227826.9","gene_symbol":"HLA-DRB4","gene_name":"major histocompatibility complex, class II, DR beta 4 [Source:HGNC Symbol;Acc:HGNC:4952]","synonyms":"HLA-DR4B,HLA-DR4B","biotype":"protein_coding","ncbi_id":"3126","summary":"HLA-DRB4 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32574846,"end":32589794,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 4 [Source:HGNC Symbol;Acc:HGNC:4952]"}, {"versioned_ensembl_gene_id":"ENSG00000229151.1","gene_symbol":"AC233976.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51356944,"end":51396462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256436.1","gene_symbol":"TAS2R31","gene_name":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]","synonyms":"T2R53,T2R31,TAS2R44","biotype":"protein_coding","ncbi_id":"259290","summary":"TAS2R44 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11030387,"end":11031407,"strand":-1,"description":"taste 2 receptor member 31 [Source:HGNC Symbol;Acc:HGNC:19113]"}, {"versioned_ensembl_gene_id":"ENSG00000282540.1","gene_symbol":"WHAMMP2","gene_name":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32360]","synonyms":"WHDC1L2,WHAMML2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440253","summary":null,"start":28879087,"end":28900706,"strand":1,"description":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32360]"}, {"versioned_ensembl_gene_id":"ENSG00000237621.3","gene_symbol":"OR9A1P","gene_name":"olfactory receptor family 9 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8486]","synonyms":"OR9A1,HTPCRX06,HSHTPCRX06","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26495","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":141887148,"end":141888092,"strand":1,"description":"olfactory receptor family 9 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8486]"}, {"versioned_ensembl_gene_id":"ENSG00000133800.8","gene_symbol":"LYVE1","gene_name":"lymphatic vessel endothelial hyaluronan receptor 1 [Source:HGNC Symbol;Acc:HGNC:14687]","synonyms":"XLKD1,LYVE-1","biotype":"protein_coding","ncbi_id":"10894","summary":"This gene encodes a type I integral membrane glycoprotein. The encoded protein acts as a receptor and binds to both soluble and immobilized hyaluronan. This protein may function in lymphatic hyaluronan transport and have a role in tumor metastasis. [provided by RefSeq, Jul 2008]","start":10556966,"end":10611689,"strand":-1,"description":"lymphatic vessel endothelial hyaluronan receptor 1 [Source:HGNC Symbol;Acc:HGNC:14687]"}, {"versioned_ensembl_gene_id":"ENSG00000213939.4","gene_symbol":"AC091153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4704816,"end":4705217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212128.2","gene_symbol":"TAS2R13","gene_name":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]","synonyms":"TRB3,T2R13","biotype":"protein_coding","ncbi_id":"50838","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10907926,"end":10909562,"strand":-1,"description":"taste 2 receptor member 13 [Source:HGNC Symbol;Acc:HGNC:14919]"}, {"versioned_ensembl_gene_id":"ENSG00000282192.1","gene_symbol":"AC067930.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143542110,"end":143542400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170801.9","gene_symbol":"HTRA3","gene_name":"HtrA serine peptidase 3 [Source:HGNC Symbol;Acc:HGNC:30406]","synonyms":"Tasp,Prsp","biotype":"protein_coding","ncbi_id":"94031","summary":null,"start":8269765,"end":8307111,"strand":1,"description":"HtrA serine peptidase 3 [Source:HGNC Symbol;Acc:HGNC:30406]"}, {"versioned_ensembl_gene_id":"ENSG00000258745.1","gene_symbol":"AL358334.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50912226,"end":50913358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226530.1","gene_symbol":"AL158055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51396511,"end":51465661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231312.6","gene_symbol":"AC007388.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39436637,"end":39665343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256188.3","gene_symbol":"TAS2R30","gene_name":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]","synonyms":"T2R30,TAS2R47","biotype":"protein_coding","ncbi_id":"259293","summary":null,"start":11132958,"end":11134644,"strand":-1,"description":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]"}, {"versioned_ensembl_gene_id":"ENSG00000100504.16","gene_symbol":"PYGL","gene_name":"glycogen phosphorylase L [Source:HGNC Symbol;Acc:HGNC:9725]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5836","summary":"This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2011]","start":50857891,"end":50944736,"strand":-1,"description":"glycogen phosphorylase L [Source:HGNC Symbol;Acc:HGNC:9725]"}, {"versioned_ensembl_gene_id":"ENSG00000187690.3","gene_symbol":"CXorf67","gene_name":"chromosome X open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:33738]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340602","summary":null,"start":51406915,"end":51408843,"strand":1,"description":"chromosome X open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:33738]"}, {"versioned_ensembl_gene_id":"ENSG00000263126.1","gene_symbol":"AC040162.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67882461,"end":67886367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226761.3","gene_symbol":"TAS2R46","gene_name":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]","synonyms":"T2R54","biotype":"protein_coding","ncbi_id":"259292","summary":"TAS2R46 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Sep 2009]","start":11061365,"end":11062294,"strand":-1,"description":"taste 2 receptor member 46 [Source:HGNC Symbol;Acc:HGNC:18877]"}, {"versioned_ensembl_gene_id":"ENSG00000065518.7","gene_symbol":"NDUFB4","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 [Source:HGNC Symbol;Acc:HGNC:7699]","synonyms":"B15","biotype":"protein_coding","ncbi_id":"4710","summary":"This gene encodes a non-catalytic subunit of the multisubunit NADH:ubiquinone oxidoreductase, the first enzyme complex in the mitochondrial electron transport chain (complex I). Mammalian complex I is composed of 45 different subunits and transfers electrons from NADH to ubiquinone. [provided by RefSeq, Dec 2009]","start":120596309,"end":120602500,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 [Source:HGNC Symbol;Acc:HGNC:7699]"}, {"versioned_ensembl_gene_id":"ENSG00000134551.12","gene_symbol":"PRH2","gene_name":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]","synonyms":"Pr","biotype":"protein_coding","ncbi_id":"5555","summary":"This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. In western population this locus is commonly biallelic and encodes proline-rich protein (PRP) isoforms, PRP-1 and PRP-2. The reference genome encodes the PRP-1 allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Oct 2015]","start":10929236,"end":10932341,"strand":1,"description":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]"}, {"versioned_ensembl_gene_id":"ENSG00000254016.2","gene_symbol":"ALG1L10P","gene_name":"asparagine-linked glycosylation 1-like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:44379]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479037","summary":null,"start":8227734,"end":8231764,"strand":1,"description":"asparagine-linked glycosylation 1-like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:44379]"}, {"versioned_ensembl_gene_id":"ENSG00000257891.1","gene_symbol":"AL929601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18920109,"end":18934078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230126.1","gene_symbol":"FGF12-AS2","gene_name":"FGF12 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40235]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873987","summary":null,"start":192515022,"end":192516573,"strand":1,"description":"FGF12 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40235]"}, {"versioned_ensembl_gene_id":"ENSG00000278186.2","gene_symbol":"GOLGA8M","gene_name":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653720","summary":null,"start":28843455,"end":28853824,"strand":-1,"description":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]"}, {"versioned_ensembl_gene_id":"ENSG00000226709.1","gene_symbol":"FGF12-AS3","gene_name":"FGF12 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40236]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873988","summary":null,"start":192516831,"end":192521398,"strand":1,"description":"FGF12 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40236]"}, {"versioned_ensembl_gene_id":"ENSG00000196368.4","gene_symbol":"NUDT11","gene_name":"nudix hydrolase 11 [Source:HGNC Symbol;Acc:HGNC:18011]","synonyms":"hDIPP3beta,FLJ10628,DIPP3b","biotype":"protein_coding","ncbi_id":"55190","summary":"NUDT11 belongs to a subgroup of phosphohydrolases that preferentially attack diphosphoinositol polyphosphates (Hidaka et al., 2002 [PubMed 12105228]).[supplied by OMIM, Mar 2008]","start":51490011,"end":51496596,"strand":-1,"description":"nudix hydrolase 11 [Source:HGNC Symbol;Acc:HGNC:18011]"}, {"versioned_ensembl_gene_id":"ENSG00000231383.2","gene_symbol":"FGF12-AS1","gene_name":"FGF12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40234]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873986","summary":null,"start":192238037,"end":192283097,"strand":1,"description":"FGF12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40234]"}, {"versioned_ensembl_gene_id":"ENSG00000213551.4","gene_symbol":"DNAJC9","gene_name":"DnaJ heat shock protein family (Hsp40) member C9 [Source:HGNC Symbol;Acc:HGNC:19123]","synonyms":"SB73,JDD1","biotype":"protein_coding","ncbi_id":"23234","summary":null,"start":73183362,"end":73248862,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C9 [Source:HGNC Symbol;Acc:HGNC:19123]"}, {"versioned_ensembl_gene_id":"ENSG00000234788.1","gene_symbol":"HSPA8P3","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44918]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420143","summary":null,"start":26714622,"end":26715832,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44918]"}, {"versioned_ensembl_gene_id":"ENSG00000164916.10","gene_symbol":"FOXK1","gene_name":"forkhead box K1 [Source:HGNC Symbol;Acc:HGNC:23480]","synonyms":"IMAGE:5164497","biotype":"protein_coding","ncbi_id":"221937","summary":null,"start":4682309,"end":4771443,"strand":1,"description":"forkhead box K1 [Source:HGNC Symbol;Acc:HGNC:23480]"}, {"versioned_ensembl_gene_id":"ENSG00000114279.13","gene_symbol":"FGF12","gene_name":"fibroblast growth factor 12 [Source:HGNC Symbol;Acc:HGNC:3668]","synonyms":"FHF1,FGF12B","biotype":"protein_coding","ncbi_id":"2257","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. [provided by RefSeq, Dec 2019]","start":192139395,"end":192767764,"strand":-1,"description":"fibroblast growth factor 12 [Source:HGNC Symbol;Acc:HGNC:3668]"}, {"versioned_ensembl_gene_id":"ENSG00000136754.17","gene_symbol":"ABI1","gene_name":"abl interactor 1 [Source:HGNC Symbol;Acc:HGNC:11320]","synonyms":"SSH3BP1,E3B1,ABI-1","biotype":"protein_coding","ncbi_id":"10006","summary":"This gene encodes a member of the Abelson-interactor family of adaptor proteins. These proteins facilitate signal transduction as components of several multiprotein complexes, and regulate actin polymerization and cytoskeletal remodeling through interactions with Abelson tyrosine kinases. The encoded protein plays a role in macropinocytosis as a component of the WAVE2 complex, and also forms a complex with EPS8 and SOS1 that mediates signal transduction from Ras to Rac. This gene may play a role in the progression of several malignancies including melanoma, colon cancer and breast cancer, and a t(10;11) chromosomal translocation involving this gene and the MLL gene has been associated with acute myeloid leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 14. [provided by RefSeq, Sep 2011]","start":26746593,"end":26861087,"strand":-1,"description":"abl interactor 1 [Source:HGNC Symbol;Acc:HGNC:11320]"}, {"versioned_ensembl_gene_id":"ENSG00000177112.7","gene_symbol":"MRVI1-AS1","gene_name":"MRVI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43434]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129827","summary":null,"start":10541272,"end":10599932,"strand":1,"description":"MRVI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43434]"}, {"versioned_ensembl_gene_id":"ENSG00000150394.13","gene_symbol":"CDH8","gene_name":"cadherin 8 [Source:HGNC Symbol;Acc:HGNC:1767]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1006","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. The extracellular domain consists of 5 subdomains, each containing a cadherin motif, and appears to determine the specificity of the protein's homophilic cell adhesion activity. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. This particular cadherin is expressed in brain and is putatively involved in synaptic adhesion, axon outgrowth and guidance. [provided by RefSeq, Jul 2008]","start":61647242,"end":62037035,"strand":-1,"description":"cadherin 8 [Source:HGNC Symbol;Acc:HGNC:1767]"}, {"versioned_ensembl_gene_id":"ENSG00000214381.4","gene_symbol":"LINC00488","gene_name":"long intergenic non-protein coding RNA 488 [Source:HGNC Symbol;Acc:HGNC:32675]","synonyms":"FLJ41232,C3orf66","biotype":"lincRNA","ncbi_id":"677779","summary":null,"start":109178165,"end":109185257,"strand":1,"description":"long intergenic non-protein coding RNA 488 [Source:HGNC Symbol;Acc:HGNC:32675]"}, {"versioned_ensembl_gene_id":"ENSG00000243861.1","gene_symbol":"AC092994.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154511535,"end":154539309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256712.1","gene_symbol":"AC134349.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11166090,"end":11171353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267226.2","gene_symbol":"AC104971.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":58670009,"end":58671877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255837.1","gene_symbol":"TAS2R20","gene_name":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]","synonyms":"TAS2R49,T2R56,T2R20","biotype":"protein_coding","ncbi_id":"259295","summary":"This gene encodes a member of the taste receptor two family of class C G-protein coupled receptors. Receptors of this family have a short extracellular N-terminus, seven transmembrane helices, three extracellular loops and three intracellular loops, and an intracellular C-terminus. Members of this family are expressed in a subset of taste receptor cells, where they function in bitter taste reception, as well as in non-gustatory cells including those of the brain, reproductive organs, respiratory system, and gastrointestinal system. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2016]","start":10996495,"end":10997875,"strand":-1,"description":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]"}, {"versioned_ensembl_gene_id":"ENSG00000243154.1","gene_symbol":"SYPL1P1","gene_name":"synaptophysin like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:53546]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130011","summary":null,"start":154651656,"end":154652423,"strand":-1,"description":"synaptophysin like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:53546]"}, {"versioned_ensembl_gene_id":"ENSG00000232645.5","gene_symbol":"LINC01431","gene_name":"long intergenic non-protein coding RNA 1431 [Source:HGNC Symbol;Acc:HGNC:50744]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505683","summary":null,"start":23356594,"end":23358116,"strand":-1,"description":"long intergenic non-protein coding RNA 1431 [Source:HGNC Symbol;Acc:HGNC:50744]"}, {"versioned_ensembl_gene_id":"ENSG00000164845.16","gene_symbol":"FAM86FP","gene_name":"family with sequence similarity 86 member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:42357]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653113","summary":null,"start":8232512,"end":8242948,"strand":-1,"description":"family with sequence similarity 86 member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:42357]"}, {"versioned_ensembl_gene_id":"ENSG00000224565.1","gene_symbol":"LINC01754","gene_name":"long intergenic non-protein coding RNA 1754 [Source:HGNC Symbol;Acc:HGNC:52542]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723442","summary":null,"start":47391929,"end":47412327,"strand":-1,"description":"long intergenic non-protein coding RNA 1754 [Source:HGNC Symbol;Acc:HGNC:52542]"}, {"versioned_ensembl_gene_id":"ENSG00000228572.7","gene_symbol":"AL954722.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":253743,"end":255091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266946.1","gene_symbol":"MRPL37P1","gene_name":"mitochondrial ribosomal protein L37 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31003]","synonyms":"HsT4307","biotype":"processed_pseudogene","ncbi_id":"100420950","summary":null,"start":58690356,"end":58692153,"strand":1,"description":"mitochondrial ribosomal protein L37 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31003]"}, {"versioned_ensembl_gene_id":"ENSG00000256274.1","gene_symbol":"AC018630.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":11076769,"end":11079171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242151.1","gene_symbol":"DYNLL1P5","gene_name":"dynein light chain LC8-type 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49656]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480681","summary":null,"start":154657294,"end":154657563,"strand":1,"description":"dynein light chain LC8-type 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49656]"}, {"versioned_ensembl_gene_id":"ENSG00000221120.1","gene_symbol":"MIR1224","gene_name":"microRNA 1224 [Source:HGNC Symbol;Acc:HGNC:33923]","synonyms":"MIRN1224,hsa-mir-1224","biotype":"miRNA","ncbi_id":"100187716","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":184241405,"end":184241489,"strand":1,"description":"microRNA 1224 [Source:HGNC Symbol;Acc:HGNC:33923]"}, {"versioned_ensembl_gene_id":"ENSG00000244066.3","gene_symbol":"RN7SL148P","gene_name":"RNA, 7SL, cytoplasmic 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:46164]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479275","summary":null,"start":244103932,"end":244104210,"strand":1,"description":"RNA, 7SL, cytoplasmic 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:46164]"}, {"versioned_ensembl_gene_id":"ENSG00000284565.1","gene_symbol":"MIR451A","gene_name":"microRNA 451a [Source:HGNC Symbol;Acc:HGNC:32053]","synonyms":"MIRN451,MIR451,hsa-mir-451","biotype":"miRNA","ncbi_id":"574411","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28861369,"end":28861440,"strand":-1,"description":"microRNA 451a [Source:HGNC Symbol;Acc:HGNC:32053]"}, {"versioned_ensembl_gene_id":"ENSG00000275424.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30053585,"end":30053688,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000206647.1","gene_symbol":"SNORA2","gene_name":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":10155072,"end":10155206,"strand":-1,"description":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]"}, {"versioned_ensembl_gene_id":"ENSG00000201442.2","gene_symbol":"Y_RNA","gene_name":"Y RNA 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{"versioned_ensembl_gene_id":"ENSG00000281822.1","gene_symbol":"RNU1-62P","gene_name":"RNA, U1 small nuclear 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:48404]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481613","summary":null,"start":72577040,"end":72577203,"strand":1,"description":"RNA, U1 small nuclear 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:48404]"}, {"versioned_ensembl_gene_id":"ENSG00000251973.1","gene_symbol":"RNU6-473P","gene_name":"RNA, U6 small nuclear 473, pseudogene [Source:HGNC Symbol;Acc:HGNC:47436]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479775","summary":null,"start":130497743,"end":130497849,"strand":-1,"description":"RNA, U6 small nuclear 473, pseudogene [Source:HGNC Symbol;Acc:HGNC:47436]"}, {"versioned_ensembl_gene_id":"ENSG00000263363.1","gene_symbol":"MIR5702","gene_name":"microRNA 5702 [Source:HGNC Symbol;Acc:HGNC:43503]","synonyms":"hsa-mir-5702","biotype":"miRNA","ncbi_id":"100847053","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":226658710,"end":226658793,"strand":-1,"description":"microRNA 5702 [Source:HGNC Symbol;Acc:HGNC:43503]"}, {"versioned_ensembl_gene_id":"ENSG00000207989.3","gene_symbol":"MIR493","gene_name":"microRNA 493 [Source:HGNC Symbol;Acc:HGNC:32082]","synonyms":"MIRN493,hsa-mir-493","biotype":"miRNA","ncbi_id":"574450","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100869060,"end":100869148,"strand":1,"description":"microRNA 493 [Source:HGNC Symbol;Acc:HGNC:32082]"}, {"versioned_ensembl_gene_id":"ENSG00000199963.1","gene_symbol":"RNU6-605P","gene_name":"RNA, U6 small nuclear 605, pseudogene [Source:HGNC Symbol;Acc:HGNC:47568]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481372","summary":null,"start":38926870,"end":38926977,"strand":1,"description":"RNA, U6 small nuclear 605, pseudogene [Source:HGNC Symbol;Acc:HGNC:47568]"}, {"versioned_ensembl_gene_id":"ENSG00000277255.1","gene_symbol":"MIR7854","gene_name":"microRNA 7854 [Source:HGNC Symbol;Acc:HGNC:50047]","synonyms":"hsa-mir-7854","biotype":"miRNA","ncbi_id":"102465840","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81533902,"end":81533966,"strand":1,"description":"microRNA 7854 [Source:HGNC Symbol;Acc:HGNC:50047]"}, {"versioned_ensembl_gene_id":"ENSG00000212279.2","gene_symbol":"SNORD77","gene_name":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692197","summary":null,"start":74490959,"end":74491028,"strand":-1,"description":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]"}, {"versioned_ensembl_gene_id":"ENSG00000284402.1","gene_symbol":"MIR7107","gene_name":"microRNA 7107 [Source:HGNC Symbol;Acc:HGNC:50006]","synonyms":"hsa-mir-7107","biotype":"miRNA","ncbi_id":"102465665","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":121444273,"end":121444352,"strand":-1,"description":"microRNA 7107 [Source:HGNC Symbol;Acc:HGNC:50006]"}, {"versioned_ensembl_gene_id":"ENSG00000265258.1","gene_symbol":"MIR4686","gene_name":"microRNA 4686 [Source:HGNC Symbol;Acc:HGNC:41601]","synonyms":"hsa-mir-4686","biotype":"miRNA","ncbi_id":"100616126","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2173063,"end":2173138,"strand":1,"description":"microRNA 4686 [Source:HGNC Symbol;Acc:HGNC:41601]"}, {"versioned_ensembl_gene_id":"ENSG00000283677.1","gene_symbol":"MIR3913-2","gene_name":"microRNA 3913-2 [Source:HGNC Symbol;Acc:HGNC:38953]","synonyms":"hsa-mir-3913-2","biotype":"miRNA","ncbi_id":"100500868","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69584723,"end":69584822,"strand":1,"description":"microRNA 3913-2 [Source:HGNC Symbol;Acc:HGNC:38953]"}, {"versioned_ensembl_gene_id":"ENSG00000275249.1","gene_symbol":"AC171558.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":372322,"end":373405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274350.1","gene_symbol":"RN7SL853P","gene_name":"RNA, 7SL, cytoplasmic 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:46869]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481153","summary":null,"start":72664577,"end":72664799,"strand":1,"description":"RNA, 7SL, cytoplasmic 853, pseudogene [Source:HGNC Symbol;Acc:HGNC:46869]"}, {"versioned_ensembl_gene_id":"ENSG00000252508.1","gene_symbol":"RNU4ATAC3P","gene_name":"RNA, U4atac small nuclear 3, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000251941.1","gene_symbol":"RNA5SP116","gene_name":"RNA, 5S ribosomal pseudogene 116 [Source:HGNC Symbol;Acc:HGNC:42914]","synonyms":"RN5S116","biotype":"rRNA","ncbi_id":"100873386","summary":null,"start":208054161,"end":208054258,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 116 [Source:HGNC Symbol;Acc:HGNC:42914]"}, {"versioned_ensembl_gene_id":"ENSG00000201096.1","gene_symbol":"RNA5SP387","gene_name":"RNA, 5S ribosomal pseudogene 387 [Source:HGNC Symbol;Acc:HGNC:43287]","synonyms":"RN5S387","biotype":"rRNA","ncbi_id":"107133508","summary":null,"start":75604173,"end":75604278,"strand":1,"description":"RNA, 5S ribosomal pseudogene 387 [Source:HGNC Symbol;Acc:HGNC:43287]"}, {"versioned_ensembl_gene_id":"ENSG00000252135.1","gene_symbol":"RNVU1-2","gene_name":"RNA, variant U1 small nuclear 2 [Source:HGNC 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particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28665659,"end":28665948,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000244033.3","gene_symbol":"RN7SL228P","gene_name":"RNA, 7SL, cytoplasmic 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:46244]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480983","summary":null,"start":117017946,"end":117018248,"strand":1,"description":"RNA, 7SL, cytoplasmic 228, pseudogene [Source:HGNC Symbol;Acc:HGNC:46244]"}, {"versioned_ensembl_gene_id":"ENSG00000252376.1","gene_symbol":"RNA5SP395","gene_name":"RNA, 5S ribosomal pseudogene 395 [Source:HGNC Symbol;Acc:HGNC:43295]","synonyms":"RN5S395","biotype":"rRNA","ncbi_id":"100873648","summary":null,"start":50463381,"end":50463498,"strand":1,"description":"RNA, 5S ribosomal pseudogene 395 [Source:HGNC Symbol;Acc:HGNC:43295]"}, {"versioned_ensembl_gene_id":"ENSG00000207420.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":176556704,"end":176556805,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201815.1","gene_symbol":"RNU6-526P","gene_name":"RNA, U6 small nuclear 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:47489]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481347","summary":null,"start":9371090,"end":9371195,"strand":-1,"description":"RNA, U6 small nuclear 526, pseudogene [Source:HGNC Symbol;Acc:HGNC:47489]"}, {"versioned_ensembl_gene_id":"ENSG00000212415.1","gene_symbol":"SNORD77","gene_name":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692197","summary":null,"start":32970727,"end":32970791,"strand":1,"description":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]"}, {"versioned_ensembl_gene_id":"ENSG00000201588.1","gene_symbol":"RNA5S2","gene_name":"RNA, 5S ribosomal 2 [Source:HGNC Symbol;Acc:HGNC:34363]","synonyms":"RN5S2","biotype":"rRNA","ncbi_id":"100169753","summary":null,"start":228612509,"end":228612627,"strand":-1,"description":"RNA, 5S ribosomal 2 [Source:HGNC Symbol;Acc:HGNC:34363]"}, {"versioned_ensembl_gene_id":"ENSG00000207161.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":147472133,"end":147472243,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221782.1","gene_symbol":"MIR548F2","gene_name":"microRNA 548f-2 [Source:HGNC Symbol;Acc:HGNC:35306]","synonyms":"MIRN548F2,hsa-mir-548f-2","biotype":"miRNA","ncbi_id":"100313771","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":212426263,"end":212426360,"strand":-1,"description":"microRNA 548f-2 [Source:HGNC Symbol;Acc:HGNC:35306]"}, {"versioned_ensembl_gene_id":"ENSG00000275109.1","gene_symbol":"MIR6504","gene_name":"microRNA 6504 [Source:HGNC Symbol;Acc:HGNC:49976]","synonyms":"hsa-mir-6504","biotype":"miRNA","ncbi_id":"102465251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81611348,"end":81611408,"strand":1,"description":"microRNA 6504 [Source:HGNC Symbol;Acc:HGNC:49976]"}, {"versioned_ensembl_gene_id":"ENSG00000212597.1","gene_symbol":"RNU6-876P","gene_name":"RNA, U6 small nuclear 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:47839]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481455","summary":null,"start":128993237,"end":128993340,"strand":-1,"description":"RNA, U6 small nuclear 876, pseudogene [Source:HGNC Symbol;Acc:HGNC:47839]"}, {"versioned_ensembl_gene_id":"ENSG00000199643.1","gene_symbol":"RNU4-90P","gene_name":"RNA, U4 small nuclear 90, pseudogene [Source:HGNC Symbol;Acc:HGNC:47026]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479600","summary":null,"start":91270727,"end":91270867,"strand":1,"description":"RNA, U4 small nuclear 90, pseudogene [Source:HGNC Symbol;Acc:HGNC:47026]"}, {"versioned_ensembl_gene_id":"ENSG00000263399.1","gene_symbol":"MIR3170","gene_name":"microRNA 3170 [Source:HGNC Symbol;Acc:HGNC:38282]","synonyms":"hsa-mir-3170","biotype":"miRNA","ncbi_id":"100422881","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98208524,"end":98208600,"strand":1,"description":"microRNA 3170 [Source:HGNC Symbol;Acc:HGNC:38282]"}, {"versioned_ensembl_gene_id":"ENSG00000201532.1","gene_symbol":"RNA5SP194","gene_name":"RNA, 5S ribosomal pseudogene 194 [Source:HGNC Symbol;Acc:HGNC:43094]","synonyms":"RN5S194","biotype":"rRNA","ncbi_id":"100873456","summary":null,"start":139012329,"end":139012441,"strand":1,"description":"RNA, 5S ribosomal pseudogene 194 [Source:HGNC Symbol;Acc:HGNC:43094]"}, {"versioned_ensembl_gene_id":"ENSG00000207967.1","gene_symbol":"MIR620","gene_name":"microRNA 620 [Source:HGNC Symbol;Acc:HGNC:32876]","synonyms":"MIRN620,hsa-mir-620","biotype":"miRNA","ncbi_id":"693205","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116148560,"end":116148654,"strand":-1,"description":"microRNA 620 [Source:HGNC Symbol;Acc:HGNC:32876]"}, {"versioned_ensembl_gene_id":"ENSG00000201711.1","gene_symbol":"RNU6-1303P","gene_name":"RNA, U6 small nuclear 1303, pseudogene [Source:HGNC Symbol;Acc:HGNC:48266]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481949","summary":null,"start":77635203,"end":77635309,"strand":-1,"description":"RNA, U6 small nuclear 1303, pseudogene [Source:HGNC Symbol;Acc:HGNC:48266]"}, {"versioned_ensembl_gene_id":"ENSG00000202297.1","gene_symbol":"RNY3P12","gene_name":"RNA, Ro-associated Y3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50888]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480315","summary":null,"start":92334463,"end":92334564,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:50888]"}, {"versioned_ensembl_gene_id":"ENSG00000275344.1","gene_symbol":"MIR6503","gene_name":"microRNA 6503 [Source:HGNC Symbol;Acc:HGNC:49968]","synonyms":"hsa-mir-6503","biotype":"miRNA","ncbi_id":"102465250","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60209071,"end":60209156,"strand":-1,"description":"microRNA 6503 [Source:HGNC Symbol;Acc:HGNC:49968]"}, {"versioned_ensembl_gene_id":"ENSG00000274066.1","gene_symbol":"MIR6514","gene_name":"microRNA 6514 [Source:HGNC Symbol;Acc:HGNC:50147]","synonyms":"hsa-mir-6514","biotype":"miRNA","ncbi_id":"102465257","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62792702,"end":62792771,"strand":-1,"description":"microRNA 6514 [Source:HGNC Symbol;Acc:HGNC:50147]"}, {"versioned_ensembl_gene_id":"ENSG00000206820.1","gene_symbol":"RNU1-138P","gene_name":"RNA, U1 small nuclear 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:48480]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480195","summary":null,"start":113420323,"end":113420486,"strand":1,"description":"RNA, U1 small nuclear 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:48480]"}, {"versioned_ensembl_gene_id":"ENSG00000200703.1","gene_symbol":"RNU6-873P","gene_name":"RNA, U6 small nuclear 873, pseudogene [Source:HGNC Symbol;Acc:HGNC:47836]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479951","summary":null,"start":87742543,"end":87742649,"strand":-1,"description":"RNA, U6 small nuclear 873, pseudogene [Source:HGNC Symbol;Acc:HGNC:47836]"}, {"versioned_ensembl_gene_id":"ENSG00000207445.1","gene_symbol":"SNORD15B","gene_name":"small nucleolar RNA, C/D box 15B [Source:HGNC Symbol;Acc:HGNC:16649]","synonyms":"U15B,RNU15B","biotype":"snoRNA","ncbi_id":"114599","summary":null,"start":75404421,"end":75404566,"strand":1,"description":"small nucleolar RNA, C/D box 15B [Source:HGNC Symbol;Acc:HGNC:16649]"}, {"versioned_ensembl_gene_id":"ENSG00000201659.1","gene_symbol":"RNU12-2P","gene_name":"RNA, U12 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:10109]","synonyms":"U12,RNU12P,RNU12","biotype":"snRNA","ncbi_id":"26823","summary":null,"start":47132671,"end":47132826,"strand":1,"description":"RNA, U12 small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:10109]"}, {"versioned_ensembl_gene_id":"ENSG00000212175.1","gene_symbol":"SNORA12","gene_name":"Small nucleolar RNA SNORA12 [Source:RFAM;Acc:RF00586]","synonyms":"U108","biotype":"snoRNA","ncbi_id":"677800","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":55565703,"end":55565850,"strand":1,"description":"Small nucleolar RNA SNORA12 [Source:RFAM;Acc:RF00586]"}, {"versioned_ensembl_gene_id":"ENSG00000252645.1","gene_symbol":"RNU7-111P","gene_name":"RNA, U7 small nuclear 111 pseudogene [Source:HGNC Symbol;Acc:HGNC:45645]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481800","summary":null,"start":89897576,"end":89897637,"strand":1,"description":"RNA, U7 small nuclear 111 pseudogene [Source:HGNC Symbol;Acc:HGNC:45645]"}, {"versioned_ensembl_gene_id":"ENSG00000263871.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32720817,"end":32720965,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000239008.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":80857076,"end":80857202,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000222610.1","gene_symbol":"RNU6-402P","gene_name":"RNA, U6 small nuclear 402, pseudogene [Source:HGNC Symbol;Acc:HGNC:47365]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481305","summary":null,"start":98889731,"end":98889833,"strand":1,"description":"RNA, U6 small nuclear 402, pseudogene [Source:HGNC Symbol;Acc:HGNC:47365]"}, {"versioned_ensembl_gene_id":"ENSG00000251763.1","gene_symbol":"RNU6-470P","gene_name":"RNA, U6 small nuclear 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:47433]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479773","summary":null,"start":43412427,"end":43412530,"strand":1,"description":"RNA, U6 small nuclear 470, pseudogene [Source:HGNC Symbol;Acc:HGNC:47433]"}, {"versioned_ensembl_gene_id":"ENSG00000276881.1","gene_symbol":"RNU6-1258P","gene_name":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480115","summary":null,"start":93437400,"end":93437510,"strand":-1,"description":"RNA, U6 small nuclear 1258, pseudogene [Source:HGNC Symbol;Acc:HGNC:48221]"}, {"versioned_ensembl_gene_id":"ENSG00000212102.1","gene_symbol":"MIR301B","gene_name":"microRNA 301b [Source:HGNC Symbol;Acc:HGNC:33667]","synonyms":"MIRN301B,hsa-mir-301b","biotype":"miRNA","ncbi_id":"100126318","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21652981,"end":21653058,"strand":1,"description":"microRNA 301b [Source:HGNC Symbol;Acc:HGNC:33667]"}, {"versioned_ensembl_gene_id":"ENSG00000243976.2","gene_symbol":"RN7SL523P","gene_name":"RNA, 7SL, cytoplasmic 523, pseudogene [Source:HGNC Symbol;Acc:HGNC:46539]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479414","summary":null,"start":100319073,"end":100319370,"strand":-1,"description":"RNA, 7SL, cytoplasmic 523, pseudogene [Source:HGNC Symbol;Acc:HGNC:46539]"}, {"versioned_ensembl_gene_id":"ENSG00000251722.1","gene_symbol":"RNU5E-3P","gene_name":"RNA, U5E small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42512]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873828","summary":null,"start":48574453,"end":48574520,"strand":-1,"description":"RNA, U5E small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:42512]"}, {"versioned_ensembl_gene_id":"ENSG00000277588.1","gene_symbol":"MIR6806","gene_name":"microRNA 6806 [Source:HGNC Symbol;Acc:HGNC:49937]","synonyms":"hsa-mir-6806","biotype":"miRNA","ncbi_id":"102465484","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58334688,"end":58334751,"strand":1,"description":"microRNA 6806 [Source:HGNC Symbol;Acc:HGNC:49937]"}, {"versioned_ensembl_gene_id":"ENSG00000207341.1","gene_symbol":"RNA5SP64","gene_name":"RNA, 5S ribosomal pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:42841]","synonyms":"RN5S64","biotype":"rRNA","ncbi_id":"100873299","summary":null,"start":166042244,"end":166042350,"strand":1,"description":"RNA, 5S ribosomal pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:42841]"}, {"versioned_ensembl_gene_id":"ENSG00000202272.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23782210,"end":23782310,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283519.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":75270700,"end":75270780,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000243532.3","gene_symbol":"RN7SL19P","gene_name":"RNA, 7SL, cytoplasmic 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:46035]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480370","summary":null,"start":70654578,"end":70654883,"strand":-1,"description":"RNA, 7SL, cytoplasmic 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:46035]"}, {"versioned_ensembl_gene_id":"ENSG00000212391.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"ACA48,SNORA48A","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":226968989,"end":226969122,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000274458.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":36438661,"end":36438788,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000207719.1","gene_symbol":"MIR623","gene_name":"microRNA 623 [Source:HGNC Symbol;Acc:HGNC:32879]","synonyms":"MIRN623,hsa-mir-623","biotype":"miRNA","ncbi_id":"693208","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99356131,"end":99356228,"strand":1,"description":"microRNA 623 [Source:HGNC Symbol;Acc:HGNC:32879]"}, {"versioned_ensembl_gene_id":"ENSG00000199121.4","gene_symbol":"MIR26B","gene_name":"microRNA 26b [Source:HGNC Symbol;Acc:HGNC:31612]","synonyms":"MIRN26B,hsa-mir-26b","biotype":"miRNA","ncbi_id":"407017","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":218402646,"end":218402722,"strand":1,"description":"microRNA 26b [Source:HGNC Symbol;Acc:HGNC:31612]"}, {"versioned_ensembl_gene_id":"ENSG00000252018.1","gene_symbol":"RNU2-30P","gene_name":"RNA, U2 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:48523]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481643","summary":null,"start":52754322,"end":52754462,"strand":1,"description":"RNA, U2 small nuclear 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:48523]"}, {"versioned_ensembl_gene_id":"ENSG00000207293.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":57169108,"end":57169209,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278204.1","gene_symbol":"MIR6857","gene_name":"microRNA 6857 [Source:HGNC Symbol;Acc:HGNC:50263]","synonyms":"hsa-mir-6857","biotype":"miRNA","ncbi_id":"102465516","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53405673,"end":53405765,"strand":-1,"description":"microRNA 6857 [Source:HGNC Symbol;Acc:HGNC:50263]"}, {"versioned_ensembl_gene_id":"ENSG00000277824.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54913845,"end":54920784,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000283690.1","gene_symbol":"MIR3116-2","gene_name":"microRNA 3116-2 [Source:HGNC Symbol;Acc:HGNC:38318]","synonyms":"hsa-mir-3116-2","biotype":"miRNA","ncbi_id":"100422946","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62078789,"end":62078856,"strand":-1,"description":"microRNA 3116-2 [Source:HGNC Symbol;Acc:HGNC:38318]"}, {"versioned_ensembl_gene_id":"ENSG00000251890.1","gene_symbol":"RNA5SP497","gene_name":"RNA, 5S ribosomal pseudogene 497 [Source:HGNC Symbol;Acc:HGNC:43397]","synonyms":"RN5S497","biotype":"rRNA","ncbi_id":"100873739","summary":null,"start":32635102,"end":32635198,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 497 [Source:HGNC Symbol;Acc:HGNC:43397]"}, {"versioned_ensembl_gene_id":"ENSG00000223293.1","gene_symbol":"RNA5SP270","gene_name":"RNA, 5S ribosomal pseudogene 270 [Source:HGNC Symbol;Acc:HGNC:43170]","synonyms":"RN5S270","biotype":"rRNA","ncbi_id":"100873523","summary":null,"start":69929905,"end":69930022,"strand":1,"description":"RNA, 5S ribosomal pseudogene 270 [Source:HGNC Symbol;Acc:HGNC:43170]"}, {"versioned_ensembl_gene_id":"ENSG00000251835.1","gene_symbol":"RNU6ATAC32P","gene_name":"RNA, U6atac small nuclear 32, 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{"versioned_ensembl_gene_id":"ENSG00000273515.1","gene_symbol":"DAOA-AS1_2","gene_name":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":103953098,"end":103953284,"strand":-1,"description":"DAOA antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02091]"}, {"versioned_ensembl_gene_id":"ENSG00000239595.3","gene_symbol":"RN7SL79P","gene_name":"RNA, 7SL, cytoplasmic 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:46095]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480943","summary":null,"start":31465543,"end":31465832,"strand":1,"description":"RNA, 7SL, cytoplasmic 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:46095]"}, {"versioned_ensembl_gene_id":"ENSG00000252444.1","gene_symbol":"RNU6-344P","gene_name":"RNA, U6 small nuclear 344, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000244194.3","gene_symbol":"RN7SL218P","gene_name":"RNA, 7SL, cytoplasmic 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:46234]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480981","summary":null,"start":74011578,"end":74011876,"strand":1,"description":"RNA, 7SL, cytoplasmic 218, pseudogene [Source:HGNC Symbol;Acc:HGNC:46234]"}, {"versioned_ensembl_gene_id":"ENSG00000242509.3","gene_symbol":"RN7SL156P","gene_name":"RNA, 7SL, cytoplasmic 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:46172]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480963","summary":null,"start":36870099,"end":36870402,"strand":1,"description":"RNA, 7SL, cytoplasmic 156, pseudogene [Source:HGNC Symbol;Acc:HGNC:46172]"}, {"versioned_ensembl_gene_id":"ENSG00000200443.1","gene_symbol":"RNU6-1066P","gene_name":"RNA, U6 small nuclear 1066, pseudogene [Source:HGNC 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[provided by RefSeq, Sep 2009]","start":53787890,"end":53787956,"strand":1,"description":"microRNA 372 [Source:HGNC Symbol;Acc:HGNC:31786]"}, {"versioned_ensembl_gene_id":"ENSG00000253084.3","gene_symbol":"RNU6-840P","gene_name":"RNA, U6 small nuclear 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:47803]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479938","summary":null,"start":35093909,"end":35093973,"strand":1,"description":"RNA, U6 small nuclear 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:47803]"}, {"versioned_ensembl_gene_id":"ENSG00000201944.1","gene_symbol":"SNORA72","gene_name":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]","synonyms":"RNU72,U72","biotype":"snoRNA","ncbi_id":"26775","summary":null,"start":205731221,"end":205731352,"strand":-1,"description":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]"}, {"versioned_ensembl_gene_id":"ENSG00000199845.1","gene_symbol":"RNA5SP375","gene_name":"RNA, 5S ribosomal pseudogene 375 [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":131792172,"end":131792231,"strand":1,"description":"microRNA 548h-5 [Source:HGNC Symbol;Acc:HGNC:41768]"}, {"versioned_ensembl_gene_id":"ENSG00000283343.1","gene_symbol":"MIR4320","gene_name":"microRNA 4320 [Source:HGNC Symbol;Acc:HGNC:38369]","synonyms":"hsa-mir-4320","biotype":"miRNA","ncbi_id":"100422865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50126499,"end":50126563,"strand":-1,"description":"microRNA 4320 [Source:HGNC Symbol;Acc:HGNC:38369]"}, {"versioned_ensembl_gene_id":"ENSG00000283359.1","gene_symbol":"MIR3977","gene_name":"microRNA 3977 [Source:HGNC Symbol;Acc:HGNC:41721]","synonyms":"hsa-mir-3977","biotype":"miRNA","ncbi_id":"100616297","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82840155,"end":82840224,"strand":1,"description":"microRNA 3977 [Source:HGNC Symbol;Acc:HGNC:41721]"}, {"versioned_ensembl_gene_id":"ENSG00000221630.3","gene_symbol":"MIR1179","gene_name":"microRNA 1179 [Source:HGNC Symbol;Acc:HGNC:35260]","synonyms":"MIRN1179,hsa-mir-1179","biotype":"miRNA","ncbi_id":"100302235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88608107,"end":88608197,"strand":1,"description":"microRNA 1179 [Source:HGNC Symbol;Acc:HGNC:35260]"}, {"versioned_ensembl_gene_id":"ENSG00000221808.1","gene_symbol":"MIR1256","gene_name":"microRNA 1256 [Source:HGNC Symbol;Acc:HGNC:35321]","synonyms":"MIRN1256,hsa-mir-1256","biotype":"miRNA","ncbi_id":"100302155","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20988314,"end":20988432,"strand":-1,"description":"microRNA 1256 [Source:HGNC Symbol;Acc:HGNC:35321]"}, {"versioned_ensembl_gene_id":"ENSG00000268592.3","gene_symbol":"RAET1E-AS1","gene_name":"RAET1E antisense RNA 1 [Source:NCBI gene;Acc:100652739]","synonyms":"RAET1G-AS1,RAET1G-AS1","biotype":"antisense_RNA","ncbi_id":"100652739","summary":null,"start":149863494,"end":149919507,"strand":1,"description":"RAET1E antisense RNA 1 [Source:NCBI gene;Acc:100652739]"}, {"versioned_ensembl_gene_id":"ENSG00000217733.2","gene_symbol":"CCT7P1","gene_name":"chaperonin containing TCP1 subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442267","summary":null,"start":149879962,"end":149881572,"strand":1,"description":"chaperonin containing TCP1 subunit 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35149]"}, {"versioned_ensembl_gene_id":"ENSG00000236658.1","gene_symbol":"AL161733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130933851,"end":130945520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240622.1","gene_symbol":"RPL7P15","gene_name":"ribosomal protein L7 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270850","summary":null,"start":124151960,"end":124153063,"strand":-1,"description":"ribosomal protein L7 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36740]"}, {"versioned_ensembl_gene_id":"ENSG00000263634.1","gene_symbol":"MIR3919","gene_name":"microRNA 3919 [Source:HGNC Symbol;Acc:HGNC:38890]","synonyms":"hsa-mir-3919","biotype":"miRNA","ncbi_id":"100500803","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159282646,"end":159282734,"strand":1,"description":"microRNA 3919 [Source:HGNC Symbol;Acc:HGNC:38890]"}, {"versioned_ensembl_gene_id":"ENSG00000264477.1","gene_symbol":"MIR5682","gene_name":"microRNA 5682 [Source:HGNC Symbol;Acc:HGNC:43477]","synonyms":"hsa-mir-5682","biotype":"miRNA","ncbi_id":"100847043","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":121049640,"end":121049715,"strand":1,"description":"microRNA 5682 [Source:HGNC Symbol;Acc:HGNC:43477]"}, {"versioned_ensembl_gene_id":"ENSG00000275818.1","gene_symbol":"MIR6818","gene_name":"microRNA 6818 [Source:HGNC Symbol;Acc:HGNC:49940]","synonyms":"hsa-mir-6818","biotype":"miRNA","ncbi_id":"102466742","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30007049,"end":30007113,"strand":1,"description":"microRNA 6818 [Source:HGNC Symbol;Acc:HGNC:49940]"}, {"versioned_ensembl_gene_id":"ENSG00000266508.1","gene_symbol":"MIR3201","gene_name":"microRNA 3201 [Source:HGNC Symbol;Acc:HGNC:38235]","synonyms":"hsa-mir-3201","biotype":"miRNA","ncbi_id":"100422916","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48274364,"end":48274415,"strand":1,"description":"microRNA 3201 [Source:HGNC Symbol;Acc:HGNC:38235]"}, {"versioned_ensembl_gene_id":"ENSG00000273606.1","gene_symbol":"MIR6776","gene_name":"microRNA 6776 [Source:HGNC Symbol;Acc:HGNC:50193]","synonyms":"hsa-mir-6776","biotype":"miRNA","ncbi_id":"102465465","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2692861,"end":2692919,"strand":-1,"description":"microRNA 6776 [Source:HGNC Symbol;Acc:HGNC:50193]"}, {"versioned_ensembl_gene_id":"ENSG00000211491.2","gene_symbol":"MIR320D1","gene_name":"microRNA 320d-1 [Source:HGNC Symbol;Acc:HGNC:35386]","synonyms":"MIRN320D1,hsa-mir-320d-1","biotype":"miRNA","ncbi_id":"100313896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40727828,"end":40727875,"strand":-1,"description":"microRNA 320d-1 [Source:HGNC Symbol;Acc:HGNC:35386]"}, {"versioned_ensembl_gene_id":"ENSG00000164520.11","gene_symbol":"RAET1E","gene_name":"retinoic acid early transcript 1E [Source:HGNC Symbol;Acc:HGNC:16793]","synonyms":"ULBP4,LETAL,bA350J20.7","biotype":"protein_coding","ncbi_id":"135250","summary":"This gene belong to the RAET1 family, which consists of major histocompatibility complex (MHC) class I-related genes located in a cluster on chromosome 6q24.2-q25.3. This and RAET1G protein differ from other RAET1 proteins in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. This protein functions as a ligand for NKG2D receptor, which is expressed on the surface of several types of immune cells, and is involved in innate and adaptive immune responses. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2011]","start":149883375,"end":149898102,"strand":-1,"description":"retinoic acid early transcript 1E [Source:HGNC Symbol;Acc:HGNC:16793]"}, {"versioned_ensembl_gene_id":"ENSG00000199157.2","gene_symbol":"MIR208A","gene_name":"microRNA 208a [Source:HGNC Symbol;Acc:HGNC:31585]","synonyms":"MIRN208A,MIRN208,hsa-mir-208a,hsa-mir-208","biotype":"miRNA","ncbi_id":"406990","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23388596,"end":23388666,"strand":-1,"description":"microRNA 208a [Source:HGNC Symbol;Acc:HGNC:31585]"}, {"versioned_ensembl_gene_id":"ENSG00000273943.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000274638.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1,CLR19.9","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54970903,"end":55006759,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000173120.14","gene_symbol":"KDM2A","gene_name":"lysine demethylase 2A [Source:HGNC Symbol;Acc:HGNC:13606]","synonyms":"LILINA,KIAA1004,JHDM1A,FLJ00115,FBXL11,FBL7,FBL11,DKFZP434M1735,CXXC8","biotype":"protein_coding","ncbi_id":"22992","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains at least six highly degenerated leucine-rich repeats. This family member plays a role in epigenetic silencing. It nucleates at CpG islands and specifically demethylates both mono- and di-methylated lysine-36 of histone H3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":67119269,"end":67258087,"strand":1,"description":"lysine demethylase 2A [Source:HGNC Symbol;Acc:HGNC:13606]"}, {"versioned_ensembl_gene_id":"ENSG00000229657.2","gene_symbol":"AL391822.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204946608,"end":204947169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159720.11","gene_symbol":"ATP6V0D1","gene_name":"ATPase H+ transporting V0 subunit d1 [Source:HGNC Symbol;Acc:HGNC:13724]","synonyms":"VPATPD,Vma6,VATX,P39,ATP6DV,ATP6D","biotype":"protein_coding","ncbi_id":"9114","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is known as the D subunit and is found ubiquitously. [provided by RefSeq, Jul 2008]","start":67438014,"end":67481237,"strand":-1,"description":"ATPase H+ transporting V0 subunit d1 [Source:HGNC Symbol;Acc:HGNC:13724]"}, {"versioned_ensembl_gene_id":"ENSG00000105011.8","gene_symbol":"ASF1B","gene_name":"anti-silencing function 1B histone chaperone [Source:HGNC Symbol;Acc:HGNC:20996]","synonyms":"FLJ10604","biotype":"protein_coding","ncbi_id":"55723","summary":"This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The encoded protein is the substrate of the tousled-like kinase family of cell cycle-regulated kinases, and may play a key role in modulating the nucleosome structure of chromatin by ensuring a constant supply of histones at sites of nucleosome assembly. [provided by RefSeq, Jul 2008]","start":14119509,"end":14136956,"strand":-1,"description":"anti-silencing function 1B histone chaperone [Source:HGNC Symbol;Acc:HGNC:20996]"}, {"versioned_ensembl_gene_id":"ENSG00000283566.2","gene_symbol":"AC243725.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21773754,"end":21783465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274180.1","gene_symbol":"NATD1","gene_name":"N-acetyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30770]","synonyms":"MGC33894,Gtlf3b,C17orf103","biotype":"protein_coding","ncbi_id":"256302","summary":null,"start":21238870,"end":21253410,"strand":-1,"description":"N-acetyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30770]"}, {"versioned_ensembl_gene_id":"ENSG00000251250.1","gene_symbol":"AC091951.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7326064,"end":7326609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250974.1","gene_symbol":"LINC02196","gene_name":"long intergenic non-protein coding RNA 2196 [Source:HGNC Symbol;Acc:HGNC:53062]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986402","summary":null,"start":6933670,"end":7190812,"strand":1,"description":"long intergenic non-protein coding RNA 2196 [Source:HGNC Symbol;Acc:HGNC:53062]"}, {"versioned_ensembl_gene_id":"ENSG00000228887.3","gene_symbol":"EEF1DP1","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126037","summary":null,"start":14070342,"end":14071237,"strand":1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32474]"}, {"versioned_ensembl_gene_id":"ENSG00000132005.8","gene_symbol":"RFX1","gene_name":"regulatory factor X1 [Source:HGNC Symbol;Acc:HGNC:9982]","synonyms":"EF-C","biotype":"protein_coding","ncbi_id":"5989","summary":"This gene encodes a member of the regulatory factor X (RFX) family of transcription factors, which are characterized by a winged-helix DNA-binding domain. The encoded transcription factor contains an N-terminal activation domain and a C-terminal repression domain, and may activate or repress target gene expression depending on cellular context. This transcription factor has been shown to regulate a wide variety of genes involved in immunity and cancer, including the MHC class II genes and genes that may be involved in cancer progression. This gene exhibits altered expression in glioblastoma and the autoimmune disease systemic lupus erythematosis (SLE). [provided by RefSeq, Jul 2016]","start":13961538,"end":14007039,"strand":-1,"description":"regulatory factor X1 [Source:HGNC Symbol;Acc:HGNC:9982]"}, {"versioned_ensembl_gene_id":"ENSG00000065600.12","gene_symbol":"TMEM206","gene_name":"transmembrane protein 206 [Source:HGNC Symbol;Acc:HGNC:25593]","synonyms":"FLJ10874,C1orf75","biotype":"protein_coding","ncbi_id":"55248","summary":null,"start":212363931,"end":212414901,"strand":-1,"description":"transmembrane protein 206 [Source:HGNC Symbol;Acc:HGNC:25593]"}, {"versioned_ensembl_gene_id":"ENSG00000158955.10","gene_symbol":"WNT9B","gene_name":"Wnt family member 9B [Source:HGNC Symbol;Acc:HGNC:12779]","synonyms":"WNT15,WNT14B","biotype":"protein_coding","ncbi_id":"7484","summary":"The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. Study of its expression in the teratocarcinoma cell line NT2 suggests that it may be implicated in the early process of neuronal differentiation of NT2 cells induced by retinoic acid. This gene is clustered with WNT3, another family member, in the chromosome 17q21 region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":46833201,"end":46886730,"strand":1,"description":"Wnt family member 9B [Source:HGNC Symbol;Acc:HGNC:12779]"}, {"versioned_ensembl_gene_id":"ENSG00000036530.8","gene_symbol":"CYP46A1","gene_name":"cytochrome P450 family 46 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2641]","synonyms":"CYP46","biotype":"protein_coding","ncbi_id":"10858","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein is expressed in the brain, where it converts cholesterol to 24S-hydroxycholesterol. While cholesterol cannot pass the blood-brain barrier, 24S-hydroxycholesterol can be secreted in the brain into the circulation to be returned to the liver for catabolism. [provided by RefSeq, Jul 2008]","start":99684304,"end":99727301,"strand":1,"description":"cytochrome P450 family 46 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2641]"}, {"versioned_ensembl_gene_id":"ENSG00000269404.6","gene_symbol":"SPIB","gene_name":"Spi-B transcription factor [Source:HGNC Symbol;Acc:HGNC:11242]","synonyms":"SPI-B","biotype":"protein_coding","ncbi_id":"6689","summary":"The protein encoded by this gene is a transcriptional activator that binds to the PU-box (5'-GAGGAA-3') and acts as a lymphoid-specific enhancer. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":50418938,"end":50431313,"strand":1,"description":"Spi-B transcription factor [Source:HGNC Symbol;Acc:HGNC:11242]"}, {"versioned_ensembl_gene_id":"ENSG00000156463.17","gene_symbol":"SH3RF2","gene_name":"SH3 domain containing ring finger 2 [Source:HGNC Symbol;Acc:HGNC:26299]","synonyms":"PPP1R39,POSHER,Hepp1,FLJ23654,RNF158","biotype":"protein_coding","ncbi_id":"153769","summary":null,"start":145936579,"end":146081791,"strand":1,"description":"SH3 domain containing ring finger 2 [Source:HGNC Symbol;Acc:HGNC:26299]"}, {"versioned_ensembl_gene_id":"ENSG00000248493.1","gene_symbol":"AC005351.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145997218,"end":145998003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204928.2","gene_symbol":"GRXCR2","gene_name":"glutaredoxin and cysteine rich domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33862]","synonyms":"DFNB101","biotype":"protein_coding","ncbi_id":"643226","summary":"This gene encodes a protein containing a glutaredoxin domain, which functions in protein S-glutathionylation. A mutation in this gene was found in a family with autoosomal recessive nonsyndromic sensorineural deafness-101. [provided by RefSeq, Jun 2014]","start":145858521,"end":145937126,"strand":-1,"description":"glutaredoxin and cysteine rich domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33862]"}, {"versioned_ensembl_gene_id":"ENSG00000213233.5","gene_symbol":"RPL23AP62","gene_name":"ribosomal protein L23a pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:36276]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271617","summary":null,"start":112461468,"end":112461920,"strand":-1,"description":"ribosomal protein L23a pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:36276]"}, {"versioned_ensembl_gene_id":"ENSG00000254968.6","gene_symbol":"AP003063.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112393118,"end":112621729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275902.1","gene_symbol":"AC139530.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81697025,"end":81697714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185359.12","gene_symbol":"HGS","gene_name":"hepatocyte growth factor-regulated tyrosine kinase substrate [Source:HGNC Symbol;Acc:HGNC:4897]","synonyms":"ZFYVE8,Vps27,Hrs","biotype":"protein_coding","ncbi_id":"9146","summary":"The protein encoded by this gene regulates endosomal sorting and plays a critical role in the recycling and degradation of membrane receptors. The encoded protein sorts monoubiquitinated membrane proteins into the multivesicular body, targeting these proteins for lysosome-dependent degradation. [provided by RefSeq, Dec 2010]","start":81683326,"end":81703138,"strand":1,"description":"hepatocyte growth factor-regulated tyrosine kinase substrate [Source:HGNC Symbol;Acc:HGNC:4897]"}, {"versioned_ensembl_gene_id":"ENSG00000188771.4","gene_symbol":"PLET1","gene_name":"placenta expressed transcript 1 [Source:HGNC Symbol;Acc:HGNC:30053]","synonyms":"C11orf34","biotype":"protein_coding","ncbi_id":"349633","summary":null,"start":112248479,"end":112260860,"strand":-1,"description":"placenta expressed transcript 1 [Source:HGNC Symbol;Acc:HGNC:30053]"}, {"versioned_ensembl_gene_id":"ENSG00000213671.3","gene_symbol":"OLA1P2","gene_name":"Obg-like ATPase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45277]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479059","summary":null,"start":20775642,"end":20776905,"strand":1,"description":"Obg-like ATPase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45277]"}, {"versioned_ensembl_gene_id":"ENSG00000262223.6","gene_symbol":"AC110285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81376001,"end":81385360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251604.1","gene_symbol":"LINC01385","gene_name":"long intergenic non-protein coding RNA 1385 [Source:HGNC Symbol;Acc:HGNC:50657]","synonyms":"TCONS_00009424","biotype":"lincRNA","ncbi_id":"106144542","summary":null,"start":73451498,"end":73453395,"strand":1,"description":"long intergenic non-protein coding RNA 1385 [Source:HGNC Symbol;Acc:HGNC:50657]"}, {"versioned_ensembl_gene_id":"ENSG00000122188.12","gene_symbol":"LAX1","gene_name":"lymphocyte transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:26005]","synonyms":"LAX,FLJ20340","biotype":"protein_coding","ncbi_id":"54900","summary":null,"start":203765176,"end":203776233,"strand":1,"description":"lymphocyte transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:26005]"}, {"versioned_ensembl_gene_id":"ENSG00000275542.1","gene_symbol":"AC027601.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81339183,"end":81339691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260005.6","gene_symbol":"AC027601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81228707,"end":81233983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248746.5","gene_symbol":"ACTN3","gene_name":"actinin alpha 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:165]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89","summary":"This gene encodes a member of the alpha-actin binding protein gene family. The encoded protein is primarily expressed in skeletal muscle and functions as a structural component of sarcomeric Z line. This protein is involved in crosslinking actin containing thin filaments. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the coding allele. The non-functional allele of this gene is associated with elite athlete status. [provided by RefSeq, Feb 2014]","start":66546395,"end":66563329,"strand":1,"description":"actinin alpha 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:165]"}, {"versioned_ensembl_gene_id":"ENSG00000250105.1","gene_symbol":"AP002748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66558866,"end":66560384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225180.7","gene_symbol":"AATK-AS1","gene_name":"AATK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40053]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388428","summary":null,"start":81165507,"end":81183164,"strand":1,"description":"AATK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40053]"}, {"versioned_ensembl_gene_id":"ENSG00000182700.4","gene_symbol":"IGIP","gene_name":"IgA inducing protein [Source:HGNC Symbol;Acc:HGNC:33847]","synonyms":"LOC492311,C5orf53","biotype":"protein_coding","ncbi_id":"492311","summary":null,"start":140125935,"end":140129392,"strand":1,"description":"IgA inducing protein [Source:HGNC Symbol;Acc:HGNC:33847]"}, {"versioned_ensembl_gene_id":"ENSG00000272808.3","gene_symbol":"AC015712.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":100849831,"end":100865457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148834.12","gene_symbol":"GSTO1","gene_name":"glutathione S-transferase omega 1 [Source:HGNC Symbol;Acc:HGNC:13312]","synonyms":"P28,GSTTLp28","biotype":"protein_coding","ncbi_id":"9446","summary":"The protein encoded by this gene is an omega class glutathione S-transferase (GST) with glutathione-dependent thiol transferase and dehydroascorbate reductase activities. GSTs are involved in the metabolism of xenobiotics and carcinogens. The encoded protein acts as a homodimer and is found in the cytoplasm. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":104235356,"end":104267459,"strand":1,"description":"glutathione S-transferase omega 1 [Source:HGNC Symbol;Acc:HGNC:13312]"}, {"versioned_ensembl_gene_id":"ENSG00000240270.1","gene_symbol":"RPL12P37","gene_name":"ribosomal protein L12 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129801","summary":null,"start":80976454,"end":80976948,"strand":1,"description":"ribosomal protein L12 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35565]"}, {"versioned_ensembl_gene_id":"ENSG00000232083.3","gene_symbol":"AC109327.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80602549,"end":80602926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244270.1","gene_symbol":"AL139099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49577392,"end":49577794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271340.1","gene_symbol":"AC120024.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80515657,"end":80515812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171246.5","gene_symbol":"NPTX1","gene_name":"neuronal pentraxin 1 [Source:HGNC Symbol;Acc:HGNC:7952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4884","summary":"NPTX1 is a member of the neuronal pentraxin gene family. Neuronal pentraxin 1 is similar to the rat NP1 gene which encodes a binding protein for the snake venom toxin taipoxin. Human NPTX1 mRNA is exclusively localized to the nervous system. [provided by RefSeq, Jul 2008]","start":80467148,"end":80477843,"strand":-1,"description":"neuronal pentraxin 1 [Source:HGNC Symbol;Acc:HGNC:7952]"}, {"versioned_ensembl_gene_id":"ENSG00000145545.11","gene_symbol":"SRD5A1","gene_name":"steroid 5 alpha-reductase 1 [Source:HGNC Symbol;Acc:HGNC:11284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6715","summary":"Steroid 5-alpha-reductase (EC 1.3.99.5) catalyzes the conversion of testosterone into the more potent androgen, dihydrotestosterone (DHT). Also see SRD5A2 (MIM 607306).[supplied by OMIM, Mar 2008]","start":6633343,"end":6674386,"strand":1,"description":"steroid 5 alpha-reductase 1 [Source:HGNC Symbol;Acc:HGNC:11284]"}, {"versioned_ensembl_gene_id":"ENSG00000270705.1","gene_symbol":"AL161669.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103207748,"end":103207789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251533.2","gene_symbol":"LINC00605","gene_name":"long intergenic non-protein coding RNA 605 [Source:HGNC Symbol;Acc:HGNC:43928]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100131366","summary":null,"start":103187221,"end":103189028,"strand":-1,"description":"long intergenic non-protein coding RNA 605 [Source:HGNC Symbol;Acc:HGNC:43928]"}, {"versioned_ensembl_gene_id":"ENSG00000165496.4","gene_symbol":"RPL10L","gene_name":"ribosomal protein L10 like [Source:HGNC Symbol;Acc:HGNC:17976]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140801","summary":"This gene encodes a protein sharing sequence similarity with ribosomal protein L10. It is not currently known whether the encoded protein is a functional ribosomal protein or whether it has evolved a function that is independent of the ribosome. This gene is intronless. [provided by RefSeq, Jul 2008]","start":46651010,"end":46651821,"strand":-1,"description":"ribosomal protein L10 like [Source:HGNC Symbol;Acc:HGNC:17976]"}, {"versioned_ensembl_gene_id":"ENSG00000106462.10","gene_symbol":"EZH2","gene_name":"enhancer of zeste 2 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3527]","synonyms":"KMT6A,KMT6,EZH1,ENX-1","biotype":"protein_coding","ncbi_id":"2146","summary":"This gene encodes a member of the Polycomb-group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein associates with the embryonic ectoderm development protein, the VAV1 oncoprotein, and the X-linked nuclear protein. This protein may play a role in the hematopoietic and central nervous systems. Multiple alternatively splcied transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Feb 2011]","start":148807383,"end":148884321,"strand":-1,"description":"enhancer of zeste 2 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:3527]"}, {"versioned_ensembl_gene_id":"ENSG00000166793.10","gene_symbol":"YPEL4","gene_name":"yippee like 4 [Source:HGNC Symbol;Acc:HGNC:18328]","synonyms":"FLJ30213","biotype":"protein_coding","ncbi_id":"219539","summary":null,"start":57645087,"end":57649944,"strand":-1,"description":"yippee like 4 [Source:HGNC Symbol;Acc:HGNC:18328]"}, {"versioned_ensembl_gene_id":"ENSG00000172409.5","gene_symbol":"CLP1","gene_name":"cleavage and polyadenylation factor I subunit 1 [Source:HGNC Symbol;Acc:HGNC:16999]","synonyms":"HEAB,hClp1","biotype":"protein_coding","ncbi_id":"10978","summary":"This gene encodes a member of the Clp1 family. The encoded protein is a multifunctional kinase which is a component of the tRNA splicing endonuclease complex and a component of the pre-mRNA cleavage complex II. This protein is implicated in tRNA, mRNA, and siRNA maturation. Mutations in this gene are associated with pontocerebellar hypoplasia type 10 (PCH10). Alternatively splice transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":57648992,"end":57661868,"strand":1,"description":"cleavage and polyadenylation factor I subunit 1 [Source:HGNC Symbol;Acc:HGNC:16999]"}, {"versioned_ensembl_gene_id":"ENSG00000120071.13","gene_symbol":"KANSL1","gene_name":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]","synonyms":"MSL1v1,KIAA1267,KIAA1267,DKFZP727C091,DKFZP727C091,CENP-36,CENP-36,NSL1,NSL1,MSL1v1","biotype":"protein_coding","ncbi_id":"284058","summary":"This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes. [provided by RefSeq, Jun 2012]","start":46029916,"end":46225389,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]"}, {"versioned_ensembl_gene_id":"ENSG00000149131.15","gene_symbol":"SERPING1","gene_name":"serpin family G member 1 [Source:HGNC Symbol;Acc:HGNC:1228]","synonyms":"HAE2,HAE1,C1NH,C1IN,C1-INH","biotype":"protein_coding","ncbi_id":"710","summary":"This gene encodes a highly glycosylated plasma protein involved in the regulation of the complement cascade. Its encoded protein, C1 inhibitor, inhibits activated C1r and C1s of the first complement component and thus regulates complement activation. It is synthesized in the liver, and its deficiency is associated with hereditary angioneurotic oedema (HANE). Alternative splicing results in multiple transcript variants encoding the same isoform. [provided by RefSeq, May 2020]","start":57597387,"end":57614853,"strand":1,"description":"serpin family G member 1 [Source:HGNC Symbol;Acc:HGNC:1228]"}, {"versioned_ensembl_gene_id":"ENSG00000262768.2","gene_symbol":"AC100791.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79800598,"end":79802529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224988.1","gene_symbol":"AL158207.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129883693,"end":129884170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280047.1","gene_symbol":"AC091825.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":142165767,"end":142168387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131507.10","gene_symbol":"NDFIP1","gene_name":"Nedd4 family interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:17592]","synonyms":"N4WBP5,MGC10924","biotype":"protein_coding","ncbi_id":"80762","summary":"The protein encoded by this gene belongs to a small group of evolutionarily conserved proteins with three transmembrane domains. It is a potential target for ubiquitination by the Nedd4 family of proteins. This protein is thought to be part of a family of integral Golgi membrane proteins. [provided by RefSeq, Jul 2008]","start":142108505,"end":142154443,"strand":1,"description":"Nedd4 family interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:17592]"}, {"versioned_ensembl_gene_id":"ENSG00000161654.9","gene_symbol":"LSM12","gene_name":"LSM12 homolog [Source:HGNC Symbol;Acc:HGNC:26407]","synonyms":"FLJ30656","biotype":"protein_coding","ncbi_id":"124801","summary":null,"start":44034635,"end":44067619,"strand":-1,"description":"LSM12 homolog [Source:HGNC Symbol;Acc:HGNC:26407]"}, {"versioned_ensembl_gene_id":"ENSG00000162734.12","gene_symbol":"PEA15","gene_name":"phosphoprotein enriched in astrocytes 15 [Source:HGNC Symbol;Acc:HGNC:8822]","synonyms":"PED,PEA-15,MAT1H,MAT1,HUMMAT1H,HMAT1","biotype":"protein_coding","ncbi_id":"8682","summary":"This gene encodes a death effector domain-containing protein that functions as a negative regulator of apoptosis. The encoded protein is an endogenous substrate for protein kinase C. This protein is also overexpressed in type 2 diabetes mellitus, where it may contribute to insulin resistance in glucose uptake. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":160205337,"end":160215376,"strand":1,"description":"phosphoprotein enriched in astrocytes 15 [Source:HGNC Symbol;Acc:HGNC:8822]"}, {"versioned_ensembl_gene_id":"ENSG00000254406.1","gene_symbol":"AP001994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119821304,"end":119822129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108813.10","gene_symbol":"DLX4","gene_name":"distal-less homeobox 4 [Source:HGNC Symbol;Acc:HGNC:2917]","synonyms":"DLX7,BP1,DLX9,DLX8","biotype":"protein_coding","ncbi_id":"1748","summary":"Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. The DLX proteins are postulated to play a role in forebrain and craniofacial development. Three transcript variants have been described for this gene, however, the full length nature of one variant has not been described. Studies of the two splice variants revealed that one encoded isoform functions as a repressor of the beta-globin gene while the other isoform lacks that function. [provided by RefSeq, Jul 2008]","start":49968970,"end":49974959,"strand":1,"description":"distal-less homeobox 4 [Source:HGNC Symbol;Acc:HGNC:2917]"}, {"versioned_ensembl_gene_id":"ENSG00000267432.5","gene_symbol":"DNAH17-AS1","gene_name":"DNAH17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48594]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100996295","summary":null,"start":78484882,"end":78503056,"strand":1,"description":"DNAH17 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48594]"}, {"versioned_ensembl_gene_id":"ENSG00000230988.3","gene_symbol":"RPL23AP11","gene_name":"ribosomal protein L23a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19808]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326294","summary":null,"start":102662240,"end":102662708,"strand":-1,"description":"ribosomal protein L23a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:19808]"}, {"versioned_ensembl_gene_id":"ENSG00000087157.18","gene_symbol":"PGS1","gene_name":"phosphatidylglycerophosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:30029]","synonyms":"DKFZP762M186","biotype":"protein_coding","ncbi_id":"9489","summary":null,"start":78378640,"end":78425114,"strand":1,"description":"phosphatidylglycerophosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:30029]"}, {"versioned_ensembl_gene_id":"ENSG00000275506.1","gene_symbol":"AC010378.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139612002,"end":139612363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161609.9","gene_symbol":"CCDC155","gene_name":"coiled-coil domain containing 155 [Source:HGNC Symbol;Acc:HGNC:26520]","synonyms":"KASH5,FLJ32658","biotype":"protein_coding","ncbi_id":"147872","summary":null,"start":49388218,"end":49417994,"strand":1,"description":"coiled-coil domain containing 155 [Source:HGNC Symbol;Acc:HGNC:26520]"}, {"versioned_ensembl_gene_id":"ENSG00000231082.1","gene_symbol":"AL731544.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80649797,"end":80653732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233353.1","gene_symbol":"RPS7P9","gene_name":"ribosomal protein S7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36998]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128756","summary":null,"start":80716483,"end":80717068,"strand":-1,"description":"ribosomal protein S7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36998]"}, {"versioned_ensembl_gene_id":"ENSG00000172292.14","gene_symbol":"CERS6","gene_name":"ceramide synthase 6 [Source:HGNC Symbol;Acc:HGNC:23826]","synonyms":"LASS6","biotype":"protein_coding","ncbi_id":"253782","summary":null,"start":168455862,"end":168775137,"strand":1,"description":"ceramide synthase 6 [Source:HGNC Symbol;Acc:HGNC:23826]"}, {"versioned_ensembl_gene_id":"ENSG00000226040.3","gene_symbol":"AC005740.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141896168,"end":141896689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279886.1","gene_symbol":"AC087645.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78250346,"end":78250932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158483.15","gene_symbol":"FAM86C1","gene_name":"family with sequence similarity 86 member C1 [Source:HGNC Symbol;Acc:HGNC:25561]","synonyms":"FLJ27199,FLJ10661,FAM86C","biotype":"protein_coding","ncbi_id":"55199","summary":null,"start":71787510,"end":71801236,"strand":1,"description":"family with sequence similarity 86 member C1 [Source:HGNC Symbol;Acc:HGNC:25561]"}, {"versioned_ensembl_gene_id":"ENSG00000214534.5","gene_symbol":"ZNF705E","gene_name":"zinc finger protein 705E [Source:HGNC Symbol;Acc:HGNC:33203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131539","summary":null,"start":71814045,"end":71821548,"strand":-1,"description":"zinc finger protein 705E [Source:HGNC Symbol;Acc:HGNC:33203]"}, {"versioned_ensembl_gene_id":"ENSG00000251591.2","gene_symbol":"AC016612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36071791,"end":36072079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273600.1","gene_symbol":"AP001877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95756959,"end":95757442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196418.12","gene_symbol":"ZNF124","gene_name":"zinc finger protein 124 [Source:HGNC Symbol;Acc:HGNC:12907]","synonyms":"HZF16,HZF-16","biotype":"protein_coding","ncbi_id":"7678","summary":"This gene encodes a protein with an amino-terminal KRAB-A box and multiple repeated Kruppel-type (C2H2) zinc finger motifs at its carboxy terminus. The encoded protein may function as a transcription factor. Expression of this gene is increased after vascular endothelial growth factor (VEGF) stimulation in human leukemia cell lines and results in inhibition of apoptotic cell death induced by irradiation or exposure to etoposide. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2014]","start":247121975,"end":247172016,"strand":-1,"description":"zinc finger protein 124 [Source:HGNC Symbol;Acc:HGNC:12907]"}, {"versioned_ensembl_gene_id":"ENSG00000224763.1","gene_symbol":"FDPSP8","gene_name":"farnesyl diphosphate synthase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39085]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401981","summary":null,"start":211660189,"end":211661277,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39085]"}, {"versioned_ensembl_gene_id":"ENSG00000184584.12","gene_symbol":"TMEM173","gene_name":"transmembrane protein 173 [Source:HGNC Symbol;Acc:HGNC:27962]","synonyms":"STING,NET23,MPYS,MITA,FLJ38577,ERIS","biotype":"protein_coding","ncbi_id":"340061","summary":"This gene encodes a five transmembrane protein that functions as a major regulator of the innate immune response to viral and bacterial infections. The encoded protein is a pattern recognition receptor that detects cytosolic nucleic acids and transmits signals that activate type I interferon responses. The encoded protein has also been shown to play a role in apoptotic signaling by associating with type II major histocompatibility complex. Mutations in this gene are the cause of infantile-onset STING-associated vasculopathy. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":139475534,"end":139482935,"strand":-1,"description":"transmembrane protein 173 [Source:HGNC Symbol;Acc:HGNC:27962]"}, {"versioned_ensembl_gene_id":"ENSG00000259081.1","gene_symbol":"AF111169.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76774284,"end":76781518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141524.15","gene_symbol":"TMC6","gene_name":"transmembrane channel like 6 [Source:HGNC Symbol;Acc:HGNC:18021]","synonyms":"LAK-4P,EVIN1,EVER1","biotype":"protein_coding","ncbi_id":"11322","summary":"Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 10 transmembrane domains and 2 leucine zipper motifs. [provided by RefSeq, Jul 2008]","start":78110458,"end":78132407,"strand":-1,"description":"transmembrane channel like 6 [Source:HGNC Symbol;Acc:HGNC:18021]"}, {"versioned_ensembl_gene_id":"ENSG00000075945.12","gene_symbol":"KIFAP3","gene_name":"kinesin associated protein 3 [Source:HGNC Symbol;Acc:HGNC:17060]","synonyms":"SMAP,KAP3,KAP-1,FLA3","biotype":"protein_coding","ncbi_id":"22920","summary":"The small G protein GDP dissociation stimulator (smg GDS) is a regulator protein having two activities on a group of small G proteins including the Rho and Rap1 family members and Ki-Ras; one is to stimulate their GDP/GTP exchange reactions, and the other is to inhibit their interactions with membranes. The protein encoded by this gene contains 9 'Armadillo' repeats and interacts with the smg GDS protein through these repeats. This protein, which is highly concentrated around the endoplasmic reticulum, is phosphorylated by v-src, and this phosphorylation reduces the affinity of the protein for smg GDS. It is thought that this protein serves as a linker between human chromosome-associated polypeptide (HCAP) and KIF3A/B, a kinesin superfamily protein in the nucleus, and that it plays a role in the interaction of chromosomes with an ATPase motor protein. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":169921326,"end":170085208,"strand":-1,"description":"kinesin associated protein 3 [Source:HGNC Symbol;Acc:HGNC:17060]"}, {"versioned_ensembl_gene_id":"ENSG00000105053.10","gene_symbol":"VRK3","gene_name":"vaccinia related kinase 3 [Source:HGNC Symbol;Acc:HGNC:18996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51231","summary":"This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. In both human and mouse, this gene has substitutions at several residues within the ATP binding motifs that in other kinases have been shown to be required for catalysis. In vitro assays indicate the protein lacks phosphorylation activity. The protein, however, likely retains its substrate binding capability. This gene is widely expressed in human tissues and its protein localizes to the nucleus. Alternative splicing results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]","start":49976467,"end":50025946,"strand":-1,"description":"vaccinia related kinase 3 [Source:HGNC Symbol;Acc:HGNC:18996]"}, {"versioned_ensembl_gene_id":"ENSG00000259059.1","gene_symbol":"PEBP1P1","gene_name":"phosphatidylethanolamine binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20054]","synonyms":"PBPP1","biotype":"processed_pseudogene","ncbi_id":"326614","summary":null,"start":96423700,"end":96424209,"strand":-1,"description":"phosphatidylethanolamine binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20054]"}, {"versioned_ensembl_gene_id":"ENSG00000267506.5","gene_symbol":"AC021683.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77546940,"end":77563243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279572.1","gene_symbol":"AC021683.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77571418,"end":77572516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267466.1","gene_symbol":"AC021683.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77563368,"end":77568695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267665.1","gene_symbol":"AC021683.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77526998,"end":77536592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254247.1","gene_symbol":"AC107953.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118982579,"end":118982875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241233.3","gene_symbol":"KRTAP5-8","gene_name":"keratin associated protein 5-8 [Source:HGNC Symbol;Acc:HGNC:23603]","synonyms":"UHSKerB,KRTAP5.8,KRTAP5-2","biotype":"protein_coding","ncbi_id":"57830","summary":null,"start":71538025,"end":71539207,"strand":1,"description":"keratin associated protein 5-8 [Source:HGNC Symbol;Acc:HGNC:23603]"}, {"versioned_ensembl_gene_id":"ENSG00000248769.1","gene_symbol":"AC139495.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69653248,"end":69654334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212952.6","gene_symbol":"BX088651.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42568865,"end":42569315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177992.9","gene_symbol":"SPATA31E1","gene_name":"SPATA31 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:26672]","synonyms":"FLJ35866,FAM75E1,C9orf79","biotype":"protein_coding","ncbi_id":"286234","summary":null,"start":87882826,"end":87888899,"strand":1,"description":"SPATA31 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:26672]"}, {"versioned_ensembl_gene_id":"ENSG00000280106.1","gene_symbol":"AC008555.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34949038,"end":34951205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225472.1","gene_symbol":"AL136366.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14317085,"end":14357908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183734.4","gene_symbol":"ASCL2","gene_name":"achaete-scute family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:739]","synonyms":"bHLHa45,ASH2,HASH2","biotype":"protein_coding","ncbi_id":"430","summary":"This gene is a member of the basic helix-loop-helix (BHLH) family of transcription factors. It activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. Involved in the determination of the neuronal precursors in the peripheral nervous system and the central nervous system. [provided by RefSeq, Jul 2008]","start":2268495,"end":2270952,"strand":-1,"description":"achaete-scute family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:739]"}, {"versioned_ensembl_gene_id":"ENSG00000231241.1","gene_symbol":"RPS3AP3","gene_name":"ribosomal protein S3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16537]","synonyms":"bA332A4.2","biotype":"processed_pseudogene","ncbi_id":"140713","summary":null,"start":37021743,"end":37021984,"strand":-1,"description":"ribosomal protein S3A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16537]"}, {"versioned_ensembl_gene_id":"ENSG00000197506.7","gene_symbol":"SLC28A3","gene_name":"solute carrier family 28 member 3 [Source:HGNC Symbol;Acc:HGNC:16484]","synonyms":"CNT3","biotype":"protein_coding","ncbi_id":"64078","summary":"Nucleoside transporters, such as SLC28A3, regulate multiple cellular processes, including neurotransmission, vascular tone, adenosine concentration in the vicinity of cell surface receptors, and transport and metabolism of nucleoside drugs. SLC28A3 shows broad specificity for pyrimidine and purine nucleosides (Ritzel et al., 2001 [PubMed 11032837]).[supplied by OMIM, Mar 2008]","start":84275457,"end":84340683,"strand":-1,"description":"solute carrier family 28 member 3 [Source:HGNC Symbol;Acc:HGNC:16484]"}, {"versioned_ensembl_gene_id":"ENSG00000274630.1","gene_symbol":"AC125257.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41867581,"end":41867736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196189.12","gene_symbol":"SEMA4A","gene_name":"semaphorin 4A [Source:HGNC Symbol;Acc:HGNC:10729]","synonyms":"SemB,SEMAB,FLJ12287,CORD10","biotype":"protein_coding","ncbi_id":"64218","summary":"This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]","start":156147366,"end":156177752,"strand":1,"description":"semaphorin 4A [Source:HGNC Symbol;Acc:HGNC:10729]"}, {"versioned_ensembl_gene_id":"ENSG00000268050.2","gene_symbol":"AL158151.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129175807,"end":129177575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272202.1","gene_symbol":"AC097358.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57078943,"end":57080101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165588.16","gene_symbol":"OTX2","gene_name":"orthodenticle homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5015","summary":"This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine. [provided by RefSeq, Jul 2012]","start":56799905,"end":56810479,"strand":-1,"description":"orthodenticle homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8522]"}, {"versioned_ensembl_gene_id":"ENSG00000178966.16","gene_symbol":"RMI1","gene_name":"RecQ mediated genome instability 1 [Source:HGNC Symbol;Acc:HGNC:25764]","synonyms":"BLAP75,FLJ12888,C9orf76","biotype":"protein_coding","ncbi_id":"80010","summary":"RMI1 is a component of protein complexes that limit DNA crossover formation via the dissolution of double Holliday junctions (Raynard et al., 2006 [PubMed 16595695]).[supplied by OMIM, Mar 2008]","start":83980711,"end":84004074,"strand":1,"description":"RecQ mediated genome instability 1 [Source:HGNC Symbol;Acc:HGNC:25764]"}, {"versioned_ensembl_gene_id":"ENSG00000107669.17","gene_symbol":"ATE1","gene_name":"arginyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:782]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11101","summary":"This gene encodes an arginyltransferase, an enzyme that is involved in posttranslational conjugation of arginine to N-terminal aspartate or glutamate residues. Conjugation of arginine to the N-terminal aspartate or glutamate targets proteins for ubiquitin-dependent degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":121740421,"end":121928801,"strand":-1,"description":"arginyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:782]"}, {"versioned_ensembl_gene_id":"ENSG00000267016.1","gene_symbol":"AC111170.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77469162,"end":77472770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258437.1","gene_symbol":"AL139193.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90675118,"end":90676294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223432.1","gene_symbol":"AC009988.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121615425,"end":121615839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158636.16","gene_symbol":"EMSY","gene_name":"EMSY, BRCA2 interacting transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:18071]","synonyms":"C11orf30","biotype":"protein_coding","ncbi_id":"56946","summary":null,"start":76444923,"end":76553025,"strand":1,"description":"EMSY, BRCA2 interacting transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:18071]"}, {"versioned_ensembl_gene_id":"ENSG00000167118.10","gene_symbol":"URM1","gene_name":"ubiquitin related modifier 1 [Source:HGNC Symbol;Acc:HGNC:28378]","synonyms":"MGC2668,C9orf74","biotype":"protein_coding","ncbi_id":"81605","summary":null,"start":128371319,"end":128392016,"strand":1,"description":"ubiquitin related modifier 1 [Source:HGNC Symbol;Acc:HGNC:28378]"}, {"versioned_ensembl_gene_id":"ENSG00000235335.2","gene_symbol":"AC016723.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167814774,"end":167941144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279686.1","gene_symbol":"AC142391.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":139442316,"end":139462707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262837.1","gene_symbol":"AC027801.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49834239,"end":49836454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182362.13","gene_symbol":"YBEY","gene_name":"ybeY metallopeptidase (putative) [Source:HGNC Symbol;Acc:HGNC:1299]","synonyms":"C21orf57","biotype":"protein_coding","ncbi_id":"54059","summary":"This gene encodes a highly conserved metalloprotein. A similar protein in bacteria acts as an endoribonuclease, and is thought to function in ribosomal RNA maturation and ribosome assembly. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":46286337,"end":46297751,"strand":1,"description":"ybeY metallopeptidase (putative) [Source:HGNC Symbol;Acc:HGNC:1299]"}, {"versioned_ensembl_gene_id":"ENSG00000121104.7","gene_symbol":"FAM117A","gene_name":"family with sequence similarity 117 member A [Source:HGNC Symbol;Acc:HGNC:24179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81558","summary":null,"start":49710332,"end":49789180,"strand":-1,"description":"family with sequence similarity 117 member A [Source:HGNC Symbol;Acc:HGNC:24179]"}, {"versioned_ensembl_gene_id":"ENSG00000163395.16","gene_symbol":"IGFN1","gene_name":"immunoglobulin-like and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24607]","synonyms":"EEF1A2BP1,DKFZp434B1231","biotype":"protein_coding","ncbi_id":"91156","summary":null,"start":201190825,"end":201228952,"strand":1,"description":"immunoglobulin-like and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24607]"}, {"versioned_ensembl_gene_id":"ENSG00000179361.17","gene_symbol":"ARID3B","gene_name":"AT-rich interaction domain 3B [Source:HGNC Symbol;Acc:HGNC:14350]","synonyms":"DRIL2,BDP","biotype":"protein_coding","ncbi_id":"10620","summary":"This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA-binding proteins. The encoded protein is homologous with two proteins that bind to the retinoblastoma gene product, and also with the mouse Bright and Drosophila dead ringer proteins. A pseudogene on chromosome 1p31 exists for this gene. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]","start":74541177,"end":74598131,"strand":1,"description":"AT-rich interaction domain 3B [Source:HGNC Symbol;Acc:HGNC:14350]"}, {"versioned_ensembl_gene_id":"ENSG00000167114.12","gene_symbol":"SLC27A4","gene_name":"solute carrier family 27 member 4 [Source:HGNC Symbol;Acc:HGNC:10998]","synonyms":"FATP4,ACSVL4","biotype":"protein_coding","ncbi_id":"10999","summary":"This gene encodes a member of a family of fatty acid transport proteins, which are involved in translocation of long-chain fatty acids cross the plasma membrane. This protein is expressed at high levels on the apical side of mature enterocytes in the small intestine, and appears to be the principal fatty acid transporter in enterocytes. Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome. Mutations in this gene have been associated with ichthyosis prematurity syndrome. [provided by RefSeq, Apr 2010]","start":128340646,"end":128361470,"strand":1,"description":"solute carrier family 27 member 4 [Source:HGNC Symbol;Acc:HGNC:10998]"}, {"versioned_ensembl_gene_id":"ENSG00000185324.21","gene_symbol":"CDK10","gene_name":"cyclin dependent kinase 10 [Source:HGNC Symbol;Acc:HGNC:1770]","synonyms":"PISSLRE","biotype":"protein_coding","ncbi_id":"8558","summary":"The protein encoded by this gene belongs to the CDK subfamily of the Ser/Thr protein kinase family. The CDK subfamily members are highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, and are known to be essential for cell cycle progression. This kinase has been shown to play a role in cellular proliferation and its function is limited to cell cycle G2-M phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":89680737,"end":89696364,"strand":1,"description":"cyclin dependent kinase 10 [Source:HGNC Symbol;Acc:HGNC:1770]"}, {"versioned_ensembl_gene_id":"ENSG00000158792.15","gene_symbol":"SPATA2L","gene_name":"spermatogenesis associated 2 like [Source:HGNC Symbol;Acc:HGNC:28393]","synonyms":"tamo,MGC26885,C16orf76","biotype":"protein_coding","ncbi_id":"124044","summary":null,"start":89696343,"end":89701705,"strand":-1,"description":"spermatogenesis associated 2 like [Source:HGNC Symbol;Acc:HGNC:28393]"}, {"versioned_ensembl_gene_id":"ENSG00000170469.10","gene_symbol":"SPATA24","gene_name":"spermatogenesis associated 24 [Source:HGNC Symbol;Acc:HGNC:27322]","synonyms":"T6441,CCDC161","biotype":"protein_coding","ncbi_id":"202051","summary":null,"start":139396563,"end":139404088,"strand":-1,"description":"spermatogenesis associated 24 [Source:HGNC Symbol;Acc:HGNC:27322]"}, {"versioned_ensembl_gene_id":"ENSG00000225885.6","gene_symbol":"AC023590.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118282139,"end":118400605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271358.1","gene_symbol":"AL137190.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96019484,"end":96019765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131484.4","gene_symbol":"AC091132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45533963,"end":45534710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164406.7","gene_symbol":"LEAP2","gene_name":"liver enriched antimicrobial peptide 2 [Source:HGNC Symbol;Acc:HGNC:29571]","synonyms":"LEAP-2","biotype":"protein_coding","ncbi_id":"116842","summary":"This gene encodes a cysteine-rich cationic antimicrobial peptide that is expressed predominantly in the liver. The mature peptide has activity against gram-positive bacteria and yeasts. [provided by RefSeq, Sep 2014]","start":132872322,"end":132875046,"strand":1,"description":"liver enriched antimicrobial peptide 2 [Source:HGNC Symbol;Acc:HGNC:29571]"}, {"versioned_ensembl_gene_id":"ENSG00000257322.5","gene_symbol":"AC138123.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93003415,"end":93215679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257210.1","gene_symbol":"NACAP3","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49490]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101928685","summary":null,"start":93124063,"end":93124543,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49490]"}, {"versioned_ensembl_gene_id":"ENSG00000257275.6","gene_symbol":"AL139020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95711747,"end":95757656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250253.3","gene_symbol":"AC117522.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85210060,"end":85210903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244355.7","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"NG25,G6D,MEGT1,C6orf23,Ly6-D","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31715356,"end":31717804,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000070444.14","gene_symbol":"MNT","gene_name":"MAX network transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:7188]","synonyms":"ROX,MXD6,MAD6,bHLHd3","biotype":"protein_coding","ncbi_id":"4335","summary":"The Myc/Max/Mad network comprises a group of transcription factors that co-interact to regulate gene-specific transcriptional activation or repression. This gene encodes a protein member of the Myc/Max/Mad network. This protein has a basic-Helix-Loop-Helix-zipper domain (bHLHzip) with which it binds the canonical DNA sequence CANNTG, known as the E box, following heterodimerization with Max proteins. This protein is likely a transcriptional repressor and an antagonist of Myc-dependent transcriptional activation and cell growth. This protein represses transcription by binding to DNA binding proteins at its N-terminal Sin3-interaction domain. [provided by RefSeq, Jul 2008]","start":2384060,"end":2401118,"strand":-1,"description":"MAX network transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:7188]"}, {"versioned_ensembl_gene_id":"ENSG00000254176.1","gene_symbol":"IGHV3-75","gene_name":"immunoglobulin heavy variable 3-75 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5625]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28407","summary":null,"start":106823687,"end":106824147,"strand":-1,"description":"immunoglobulin heavy variable 3-75 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5625]"}, {"versioned_ensembl_gene_id":"ENSG00000260766.1","gene_symbol":"AL513302.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":160024953,"end":160026794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237409.2","gene_symbol":"AL513302.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160020300,"end":160020727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225279.1","gene_symbol":"AL121987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160062488,"end":160079821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262921.1","gene_symbol":"AC118754.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4565752,"end":4571760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070495.14","gene_symbol":"JMJD6","gene_name":"arginine demethylase and lysine hydroxylase [Source:HGNC Symbol;Acc:HGNC:19355]","synonyms":"PTDSR1,PTDSR,KIAA0585","biotype":"protein_coding","ncbi_id":"23210","summary":"This gene encodes a nuclear protein with a JmjC domain. JmjC domain-containing proteins are predicted to function as protein hydroxylases or histone demethylases. This protein was first identified as a putative phosphatidylserine receptor involved in phagocytosis of apoptotic cells; however, subsequent studies have indicated that it does not directly function in the clearance of apoptotic cells, and questioned whether it is a true phosphatidylserine receptor. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":76712832,"end":76726799,"strand":-1,"description":"arginine demethylase and lysine hydroxylase [Source:HGNC Symbol;Acc:HGNC:19355]"}, {"versioned_ensembl_gene_id":"ENSG00000283571.1","gene_symbol":"AC245369.8","gene_name":null,"synonyms":null,"biotype":"IG_pseudogene","ncbi_id":null,"summary":null,"start":106750289,"end":106750594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225182.1","gene_symbol":"AC092601.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166889502,"end":166889884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267543.1","gene_symbol":"AC015802.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":76549951,"end":76550826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279878.1","gene_symbol":"AP003108.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61525708,"end":61526602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260698.1","gene_symbol":"AL591848.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":246682108,"end":246685075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162897.14","gene_symbol":"FCAMR","gene_name":"Fc fragment of IgA and IgM receptor [Source:HGNC Symbol;Acc:HGNC:24692]","synonyms":"FKSG87,FCA/MR,CD351","biotype":"protein_coding","ncbi_id":"83953","summary":null,"start":206957965,"end":206970625,"strand":-1,"description":"Fc fragment of IgA and IgM receptor [Source:HGNC Symbol;Acc:HGNC:24692]"}, {"versioned_ensembl_gene_id":"ENSG00000109919.9","gene_symbol":"MTCH2","gene_name":"mitochondrial carrier 2 [Source:HGNC Symbol;Acc:HGNC:17587]","synonyms":"SLC25A50","biotype":"protein_coding","ncbi_id":"23788","summary":"This gene encodes a member of the SLC25 family of nuclear-encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome-wide association studies in human have identified single-nucleotide polymorphisms in several loci associated with obesity. This gene is one such locus, which is highly expressed in white adipose tissue and adipocytes, and thought to play a regulatory role in adipocyte differentiation and biology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target that can produce two isoforms from the same mRNA by use of alternative in-frame translation termination codons. [provided by RefSeq, Dec 2017]","start":47617315,"end":47642623,"strand":-1,"description":"mitochondrial carrier 2 [Source:HGNC Symbol;Acc:HGNC:17587]"}, {"versioned_ensembl_gene_id":"ENSG00000170956.16","gene_symbol":"CEACAM3","gene_name":"carcinoembryonic antigen related cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:1815]","synonyms":"CGM1,CD66d","biotype":"protein_coding","ncbi_id":"1084","summary":"This gene encodes a member of the family of carcinoembryonic antigen-related cell adhesion molecules (CEACAMs), which are used by several bacterial pathogens to bind and invade host cells. The encoded transmembrane protein directs phagocytosis of several bacterial species that is dependent on the small GTPase Rac. It is thought to serve an important role in controlling human-specific pathogens by the innate immune system. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2013]","start":41796437,"end":41811553,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:1815]"}, {"versioned_ensembl_gene_id":"ENSG00000129038.15","gene_symbol":"LOXL1","gene_name":"lysyl oxidase like 1 [Source:HGNC Symbol;Acc:HGNC:6665]","synonyms":"LOXL,LOL","biotype":"protein_coding","ncbi_id":"4016","summary":"This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome. [provided by RefSeq, Jan 2016]","start":73925989,"end":73952137,"strand":1,"description":"lysyl oxidase like 1 [Source:HGNC Symbol;Acc:HGNC:6665]"}, {"versioned_ensembl_gene_id":"ENSG00000254456.5","gene_symbol":"AC090592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25734770,"end":25781758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227748.1","gene_symbol":"AL138916.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146859181,"end":146863081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085741.12","gene_symbol":"WNT11","gene_name":"Wnt family member 11 [Source:HGNC Symbol;Acc:HGNC:12776]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7481","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 97%, 85%, and 63% amino acid identity with mouse, chicken, and Xenopus Wnt11 protein, respectively. This gene may play roles in the development of skeleton, kidney and lung, and is considered to be a plausible candidate gene for High Bone Mass Syndrome. [provided by RefSeq, Jul 2008]","start":76186325,"end":76210736,"strand":-1,"description":"Wnt family member 11 [Source:HGNC Symbol;Acc:HGNC:12776]"}, {"versioned_ensembl_gene_id":"ENSG00000258827.2","gene_symbol":"AL079304.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37097062,"end":37098563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167208.14","gene_symbol":"SNX20","gene_name":"sorting nexin 20 [Source:HGNC Symbol;Acc:HGNC:30390]","synonyms":"SLIC1,SLIC-1","biotype":"protein_coding","ncbi_id":"124460","summary":"SNX20 interacts with the cytoplasmic domain of PSGL1 (SELPLG; MIM 600738) and cycles PSGL1 into endosomes.[supplied by OMIM, Feb 2010]","start":50666300,"end":50681353,"strand":-1,"description":"sorting nexin 20 [Source:HGNC Symbol;Acc:HGNC:30390]"}, {"versioned_ensembl_gene_id":"ENSG00000272203.1","gene_symbol":"AC004775.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132817248,"end":132818000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198944.5","gene_symbol":"SOWAHA","gene_name":"sosondowah ankyrin repeat domain family member A [Source:HGNC Symbol;Acc:HGNC:27033]","synonyms":"ANKRD43","biotype":"protein_coding","ncbi_id":"134548","summary":null,"start":132813587,"end":132816797,"strand":1,"description":"sosondowah ankyrin repeat domain family member A [Source:HGNC Symbol;Acc:HGNC:27033]"}, {"versioned_ensembl_gene_id":"ENSG00000131115.15","gene_symbol":"ZNF227","gene_name":"zinc finger protein 227 [Source:HGNC Symbol;Acc:HGNC:13020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7770","summary":null,"start":44207547,"end":44237268,"strand":1,"description":"zinc finger protein 227 [Source:HGNC Symbol;Acc:HGNC:13020]"}, {"versioned_ensembl_gene_id":"ENSG00000249820.1","gene_symbol":"AC055753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133409955,"end":133410843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249993.1","gene_symbol":"BFSP2-AS1","gene_name":"BFSP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28425]","synonyms":"MGC2848","biotype":"antisense_RNA","ncbi_id":"85003","summary":null,"start":133429269,"end":133455776,"strand":-1,"description":"BFSP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28425]"}, {"versioned_ensembl_gene_id":"ENSG00000234488.1","gene_symbol":"AC096664.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63684305,"end":63684710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101076.16","gene_symbol":"HNF4A","gene_name":"hepatocyte nuclear factor 4 alpha [Source:HGNC Symbol;Acc:HGNC:5024]","synonyms":"HNF4,TCF14,NR2A1,MODY1,MODY","biotype":"protein_coding","ncbi_id":"3172","summary":"The protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012]","start":44355700,"end":44434596,"strand":1,"description":"hepatocyte nuclear factor 4 alpha [Source:HGNC Symbol;Acc:HGNC:5024]"}, {"versioned_ensembl_gene_id":"ENSG00000253169.2","gene_symbol":"IGHVII-65-1","gene_name":"immunoglobulin heavy variable (II)-65-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5688]","synonyms":"IGHV(II)-65-1","biotype":"IG_V_pseudogene","ncbi_id":"28359","summary":null,"start":106671772,"end":106672073,"strand":-1,"description":"immunoglobulin heavy variable (II)-65-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5688]"}, {"versioned_ensembl_gene_id":"ENSG00000183837.9","gene_symbol":"PNMA3","gene_name":"paraneoplastic Ma antigen 3 [Source:HGNC Symbol;Acc:HGNC:18742]","synonyms":"MGC132758,MGC132756,MA5,MA3","biotype":"protein_coding","ncbi_id":"29944","summary":"The protein encoded by this gene belongs to the paraneoplastic antigen MA (PNMA) family, which shares homology with retroviral Gag proteins. The PNMA antigens are highly expressed in the brain and also in a range of tumors associated with serious neurological phenotypes. PMID:16407312 reports the presence of a functional -1 ribosomal frameshift signal (consisting of a heptanucleotide shift motif followed 3' by a pseudoknot structure) in this gene, however, the frame-shifted product has not been characterized. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":153056409,"end":153060467,"strand":1,"description":"paraneoplastic Ma antigen 3 [Source:HGNC Symbol;Acc:HGNC:18742]"}, {"versioned_ensembl_gene_id":"ENSG00000248905.8","gene_symbol":"FMN1","gene_name":"formin 1 [Source:HGNC Symbol;Acc:HGNC:3768]","synonyms":"MGC125288,LD,FMN,FLJ45135,DKFZP686C2281,MGC125289","biotype":"protein_coding","ncbi_id":"342184","summary":"This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]","start":32765545,"end":33194733,"strand":-1,"description":"formin 1 [Source:HGNC Symbol;Acc:HGNC:3768]"}, {"versioned_ensembl_gene_id":"ENSG00000119402.16","gene_symbol":"FBXW2","gene_name":"F-box and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:13608]","synonyms":"Md6,Fwd2,FBW2","biotype":"protein_coding","ncbi_id":"26190","summary":"F-box proteins are an expanding family of eukaryotic proteins characterized by an approximately 40 amino acid motif, the F box. Some F-box proteins have been shown to be critical for the ubiquitin-mediated degradation of cellular regulatory proteins. In fact, F-box proteins are one of the four subunits of ubiquitin protein ligases, called SCFs. SCF ligases bring ubiquitin conjugating enzymes to substrates that are specifically recruited by the different F-box proteins. Mammalian F-box proteins are classified into three groups based on the presence of either WD-40 repeats, leucine-rich repeats, or the presence or absence of other protein-protein interacting domains. This gene encodes the second identified member of the F-box gene family and contains multiple WD-40 repeats. [provided by RefSeq, Jul 2008]","start":120751978,"end":120793412,"strand":-1,"description":"F-box and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:13608]"}, {"versioned_ensembl_gene_id":"ENSG00000253936.1","gene_symbol":"IGHV3-63","gene_name":"immunoglobulin heavy variable 3-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5616]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28415","summary":null,"start":106652237,"end":106652681,"strand":-1,"description":"immunoglobulin heavy variable 3-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5616]"}, {"versioned_ensembl_gene_id":"ENSG00000229979.1","gene_symbol":"AC243428.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153052150,"end":153052413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254329.1","gene_symbol":"IGHVII-60-1","gene_name":"immunoglobulin heavy variable (II)-60-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5686]","synonyms":"IGHV(II)-60-1","biotype":"IG_V_pseudogene","ncbi_id":"28361","summary":null,"start":106637718,"end":106637973,"strand":-1,"description":"immunoglobulin heavy variable (II)-60-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5686]"}, {"versioned_ensembl_gene_id":"ENSG00000255537.1","gene_symbol":"AP000708.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":125495214,"end":125499528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239969.5","gene_symbol":"AC091390.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102364162,"end":102380633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224373.3","gene_symbol":"IGHV4-59","gene_name":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28392","summary":null,"start":106627249,"end":106627825,"strand":-1,"description":"immunoglobulin heavy variable 4-59 [Source:HGNC Symbol;Acc:HGNC:5654]"}, {"versioned_ensembl_gene_id":"ENSG00000267747.1","gene_symbol":"AC068675.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43544785,"end":43610338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211967.3","gene_symbol":"IGHV3-53","gene_name":"immunoglobulin heavy variable 3-53 [Source:HGNC Symbol;Acc:HGNC:5610]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28420","summary":null,"start":106592676,"end":106593347,"strand":-1,"description":"immunoglobulin heavy variable 3-53 [Source:HGNC Symbol;Acc:HGNC:5610]"}, {"versioned_ensembl_gene_id":"ENSG00000260624.1","gene_symbol":"AC018943.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73870950,"end":73873366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254167.1","gene_symbol":"IGHVIII-51-1","gene_name":"immunoglobulin heavy variable (III)-51-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5704]","synonyms":"IGHV(III)-51-1","biotype":"IG_V_pseudogene","ncbi_id":"28343","summary":null,"start":106583506,"end":106583807,"strand":-1,"description":"immunoglobulin heavy variable (III)-51-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5704]"}, {"versioned_ensembl_gene_id":"ENSG00000231007.5","gene_symbol":"CDC20P1","gene_name":"cell division cycle 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29487]","synonyms":"CDC20P,OTTHUMG00000020142","biotype":"processed_pseudogene","ncbi_id":"157956","summary":null,"start":87011652,"end":87013151,"strand":1,"description":"cell division cycle 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29487]"}, {"versioned_ensembl_gene_id":"ENSG00000175854.11","gene_symbol":"SWI5","gene_name":"SWI5 homologous recombination repair protein [Source:HGNC Symbol;Acc:HGNC:31412]","synonyms":"bA395P17.9,SAE3,C9orf119","biotype":"protein_coding","ncbi_id":"375757","summary":null,"start":128275379,"end":128288990,"strand":1,"description":"SWI5 homologous recombination repair protein [Source:HGNC Symbol;Acc:HGNC:31412]"}, {"versioned_ensembl_gene_id":"ENSG00000163602.10","gene_symbol":"RYBP","gene_name":"RING1 and YY1 binding protein [Source:HGNC Symbol;Acc:HGNC:10480]","synonyms":"DEDAF,YEAF1,AAP1,DEDAF,APAP-1,AAP1,YEAF1","biotype":"protein_coding","ncbi_id":"23429","summary":null,"start":72371825,"end":72446621,"strand":-1,"description":"RING1 and YY1 binding protein [Source:HGNC Symbol;Acc:HGNC:10480]"}, {"versioned_ensembl_gene_id":"ENSG00000146411.5","gene_symbol":"SLC2A12","gene_name":"solute carrier family 2 member 12 [Source:HGNC Symbol;Acc:HGNC:18067]","synonyms":"GLUT8,GLUT12","biotype":"protein_coding","ncbi_id":"154091","summary":"SLC2A12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Rogers et al., 2002). This family of transporters show conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]","start":133988697,"end":134052636,"strand":-1,"description":"solute carrier family 2 member 12 [Source:HGNC Symbol;Acc:HGNC:18067]"}, {"versioned_ensembl_gene_id":"ENSG00000164756.12","gene_symbol":"SLC30A8","gene_name":"solute carrier family 30 member 8 [Source:HGNC Symbol;Acc:HGNC:20303]","synonyms":"ZNT8,ZnT-8","biotype":"protein_coding","ncbi_id":"169026","summary":"The protein encoded by this gene is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles. This gene is expressed at a high level only in the pancreas, particularly in islets of Langerhans. The encoded protein colocalizes with insulin in the secretory pathway granules of the insulin-secreting INS-1 cells. Allelic variants of this gene exist that confer susceptibility to diabetes mellitus, noninsulin-dependent (NIDDM). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]","start":116950273,"end":117176714,"strand":1,"description":"solute carrier family 30 member 8 [Source:HGNC Symbol;Acc:HGNC:20303]"}, {"versioned_ensembl_gene_id":"ENSG00000253271.2","gene_symbol":"AC027419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117055818,"end":117056145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205250.8","gene_symbol":"E2F4","gene_name":"E2F transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:3118]","synonyms":"E2F-4","biotype":"protein_coding","ncbi_id":"1874","summary":"The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein binds to all three of the tumor suppressor proteins pRB, p107 and p130, but with higher affinity to the last two. It plays an important role in the suppression of proliferation-associated genes, and its gene mutation and increased expression may be associated with human cancer. [provided by RefSeq, Jul 2008]","start":67192169,"end":67198918,"strand":1,"description":"E2F transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:3118]"}, {"versioned_ensembl_gene_id":"ENSG00000277803.1","gene_symbol":"AC099842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23886135,"end":23893557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042088.13","gene_symbol":"TDP1","gene_name":"tyrosyl-DNA phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:18884]","synonyms":"SCAN1,FLJ11090","biotype":"protein_coding","ncbi_id":"55775","summary":"The protein encoded by this gene is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. This protein may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains. Mutations in this gene are associated with the disease spinocerebellar ataxia with axonal neuropathy (SCAN1). [provided by RefSeq, Aug 2016]","start":89954939,"end":90044768,"strand":1,"description":"tyrosyl-DNA phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:18884]"}, {"versioned_ensembl_gene_id":"ENSG00000197599.12","gene_symbol":"CCDC154","gene_name":"coiled-coil domain containing 154 [Source:HGNC Symbol;Acc:HGNC:34454]","synonyms":"LOC645811,C16orf29","biotype":"protein_coding","ncbi_id":"645811","summary":null,"start":1434383,"end":1444556,"strand":-1,"description":"coiled-coil domain containing 154 [Source:HGNC Symbol;Acc:HGNC:34454]"}, {"versioned_ensembl_gene_id":"ENSG00000169122.11","gene_symbol":"FAM110B","gene_name":"family with sequence similarity 110 member B [Source:HGNC Symbol;Acc:HGNC:28587]","synonyms":"MGC39325,C8orf72","biotype":"protein_coding","ncbi_id":"90362","summary":null,"start":57994509,"end":58204279,"strand":1,"description":"family with sequence similarity 110 member B [Source:HGNC Symbol;Acc:HGNC:28587]"}, {"versioned_ensembl_gene_id":"ENSG00000229022.1","gene_symbol":"AL365366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":241831935,"end":241832787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276310.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769748,"end":54784069,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284395.1","gene_symbol":"AL032819.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1431035,"end":1433397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231413.1","gene_symbol":"AL356289.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48078787,"end":48082196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237180.1","gene_symbol":"CYP46A4P","gene_name":"cytochrome P450 family 46 subfamily A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42349]","synonyms":"CYP46A-se1[12:13:14]","biotype":"processed_pseudogene","ncbi_id":"100874494","summary":null,"start":48089368,"end":48089634,"strand":1,"description":"cytochrome P450 family 46 subfamily A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:42349]"}, {"versioned_ensembl_gene_id":"ENSG00000059122.16","gene_symbol":"FLYWCH1","gene_name":"FLYWCH-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:25404]","synonyms":"DKFZp761A132","biotype":"protein_coding","ncbi_id":"84256","summary":null,"start":2911937,"end":2951208,"strand":1,"description":"FLYWCH-type zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:25404]"}, {"versioned_ensembl_gene_id":"ENSG00000236307.2","gene_symbol":"EEF1E1P1","gene_name":"eukaryotic translation elongation factor 1 epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51459]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130388","summary":null,"start":111887914,"end":111888741,"strand":1,"description":"eukaryotic translation elongation factor 1 epsilon 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51459]"}, {"versioned_ensembl_gene_id":"ENSG00000249725.1","gene_symbol":"AC079942.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133015004,"end":133037052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277161.1","gene_symbol":"PIGW","gene_name":"phosphatidylinositol glycan anchor biosynthesis class W [Source:HGNC Symbol;Acc:HGNC:23213]","synonyms":"Gwt1,FLJ37433","biotype":"protein_coding","ncbi_id":"284098","summary":"The protein encoded by this gene is an inositol acyltransferase that acylates the inositol ring of phosphatidylinositol. This occurs in the endoplasmic reticulum and is a step in the biosynthesis of glycosylphosphatidylinositol (GPI), which anchors many cell surface proteins to the membrane. Defects in this gene are a cause of the age-dependent epileptic encephalopathy West syndrome as well as a syndrome exhibiting hyperphosphatasia and cognitive disability (HPMRS5). [provided by RefSeq, Jul 2017]","start":36535020,"end":36539310,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class W [Source:HGNC Symbol;Acc:HGNC:23213]"}, {"versioned_ensembl_gene_id":"ENSG00000228283.3","gene_symbol":"KATNBL1P6","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49056]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729176","summary":null,"start":146802359,"end":146803824,"strand":-1,"description":"katanin regulatory subunit B1 like 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49056]"}, {"versioned_ensembl_gene_id":"ENSG00000197296.5","gene_symbol":"FITM2","gene_name":"fat storage inducing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:16135]","synonyms":"FIT2,dJ881L22.2,C20orf142","biotype":"protein_coding","ncbi_id":"128486","summary":"FIT2 belongs to an evolutionarily conserved family of proteins involved in fat storage (Kadereit et al., 2008 [PubMed 18160536]).[supplied by OMIM, May 2008]","start":44302838,"end":44311169,"strand":-1,"description":"fat storage inducing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:16135]"}, {"versioned_ensembl_gene_id":"ENSG00000177125.5","gene_symbol":"ZBTB34","gene_name":"zinc finger and BTB domain containing 34 [Source:HGNC Symbol;Acc:HGNC:31446]","synonyms":"ZNF918,MGC24652,KIAA1993","biotype":"protein_coding","ncbi_id":"403341","summary":null,"start":126860665,"end":126885878,"strand":1,"description":"zinc finger and BTB domain containing 34 [Source:HGNC Symbol;Acc:HGNC:31446]"}, {"versioned_ensembl_gene_id":"ENSG00000178773.14","gene_symbol":"CPNE7","gene_name":"copine 7 [Source:HGNC Symbol;Acc:HGNC:2320]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27132","summary":"This gene encodes a member of the copine family, which is composed of calcium-dependent membrane-binding proteins. The gene product contains two N-terminal C2 domains and one von Willebrand factor A domain. The encoded protein may be involved in membrane trafficking. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":89575768,"end":89597246,"strand":1,"description":"copine 7 [Source:HGNC Symbol;Acc:HGNC:2320]"}, {"versioned_ensembl_gene_id":"ENSG00000174914.2","gene_symbol":"OR9G1","gene_name":"olfactory receptor family 9 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:15319]","synonyms":"OR9G5","biotype":"protein_coding","ncbi_id":"390174","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56699095,"end":56703884,"strand":1,"description":"olfactory receptor family 9 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:15319]"}, {"versioned_ensembl_gene_id":"ENSG00000169155.9","gene_symbol":"ZBTB43","gene_name":"zinc finger and BTB domain containing 43 [Source:HGNC Symbol;Acc:HGNC:17908]","synonyms":"ZNF297B,ZNF-X,ZBTB22B,KIAA0414,FLJ22470","biotype":"protein_coding","ncbi_id":"23099","summary":null,"start":126805006,"end":126838210,"strand":1,"description":"zinc finger and BTB domain containing 43 [Source:HGNC Symbol;Acc:HGNC:17908]"}, {"versioned_ensembl_gene_id":"ENSG00000124194.16","gene_symbol":"GDAP1L1","gene_name":"ganglioside induced differentiation associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:4213]","synonyms":null,"biotype":"protein_coding","ncbi_id":"78997","summary":"The ganglioside GD3 synthase causes cell differentiation with neurite sprouting when transfected into the mouse neuroblastoma cell line Neuro2a. After differentiation, the expression of several genes is upregulated, including one that encodes a protein termed ganglioside-induced differentiation-associated protein 1 (Gdap1). A similar gene was found in humans, and mutations in the human gene are associated with Charcot-Marie-Tooth type 4A disease. The protein encoded by this gene is similar in sequence to the human GDAP1 protein. Several transcript variants encoding different isoforms, as well as a noncoding transcript variant, have been found for this gene. [provided by RefSeq, Feb 2012]","start":44247099,"end":44280917,"strand":1,"description":"ganglioside induced differentiation associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:4213]"}, {"versioned_ensembl_gene_id":"ENSG00000132823.10","gene_symbol":"OSER1","gene_name":"oxidative stress responsive serine rich 1 [Source:HGNC Symbol;Acc:HGNC:16105]","synonyms":"C20orf111,Perit1,Osr1,HSPC207,dJ1183I21.1","biotype":"protein_coding","ncbi_id":"51526","summary":null,"start":44196496,"end":44210791,"strand":-1,"description":"oxidative stress responsive serine rich 1 [Source:HGNC Symbol;Acc:HGNC:16105]"}, {"versioned_ensembl_gene_id":"ENSG00000254143.1","gene_symbol":"AC022733.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40161458,"end":40172612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203987.2","gene_symbol":"AL772363.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137867925,"end":137892570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233622.2","gene_symbol":"CYP2T1P","gene_name":"cytochrome P450 family 2 subfamily T member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18852]","synonyms":"CYP2T2P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"171523","summary":null,"start":40808474,"end":40811390,"strand":-1,"description":"cytochrome P450 family 2 subfamily T member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18852]"}, {"versioned_ensembl_gene_id":"ENSG00000110218.8","gene_symbol":"PANX1","gene_name":"pannexin 1 [Source:HGNC Symbol;Acc:HGNC:8599]","synonyms":"UNQ2529,PX1,MRS1","biotype":"protein_coding","ncbi_id":"24145","summary":"The protein encoded by this gene belongs to the innexin family. Innexin family members are the structural components of gap junctions. This protein and pannexin 2 are abundantly expressed in central nerve system (CNS) and are coexpressed in various neuronal populations. Studies in Xenopus oocytes suggest that this protein alone and in combination with pannexin 2 may form cell type-specific gap junctions with distinct properties. [provided by RefSeq, Jul 2008]","start":94128928,"end":94181972,"strand":1,"description":"pannexin 1 [Source:HGNC Symbol;Acc:HGNC:8599]"}, {"versioned_ensembl_gene_id":"ENSG00000165118.14","gene_symbol":"C9orf64","gene_name":"chromosome 9 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:28144]","synonyms":"MGC10999","biotype":"protein_coding","ncbi_id":"84267","summary":null,"start":83938311,"end":83956986,"strand":-1,"description":"chromosome 9 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:28144]"}, {"versioned_ensembl_gene_id":"ENSG00000258300.2","gene_symbol":"NUTF2P2","gene_name":"nuclear transport factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19934]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326613","summary":null,"start":35819837,"end":35820220,"strand":1,"description":"nuclear transport factor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19934]"}, {"versioned_ensembl_gene_id":"ENSG00000267260.1","gene_symbol":"AC020928.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36773153,"end":36777078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239201.1","gene_symbol":"AC025164.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92168400,"end":92168877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224920.1","gene_symbol":"TACC1P1","gene_name":"transforming acidic coiled-coil containing protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44974]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"219752","summary":null,"start":37523011,"end":37544701,"strand":1,"description":"transforming acidic coiled-coil containing protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44974]"}, {"versioned_ensembl_gene_id":"ENSG00000250310.1","gene_symbol":"AC006487.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49544847,"end":49577962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275923.1","gene_symbol":"AL160413.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55504906,"end":55505215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149182.14","gene_symbol":"ARFGAP2","gene_name":"ADP ribosylation factor GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:13504]","synonyms":"ZNF289,Zfp289,IRZ,FLJ14576","biotype":"protein_coding","ncbi_id":"84364","summary":null,"start":47164299,"end":47177125,"strand":-1,"description":"ADP ribosylation factor GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:13504]"}, {"versioned_ensembl_gene_id":"ENSG00000276241.1","gene_symbol":"AC243829.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36116177,"end":36177510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188404.8","gene_symbol":"SELL","gene_name":"selectin L [Source:HGNC Symbol;Acc:HGNC:10720]","synonyms":"PLNHR,LYAM1,Lyam-1,LSEL,LNHR,Leu-8,LAM1,LAM-1,hLHRc,CD62L","biotype":"protein_coding","ncbi_id":"6402","summary":"This gene encodes a cell surface adhesion molecule that belongs to a family of adhesion/homing receptors. The encoded protein contains a C-type lectin-like domain, a calcium-binding epidermal growth factor-like domain, and two short complement-like repeats. The gene product is required for binding and subsequent rolling of leucocytes on endothelial cells, facilitating their migration into secondary lymphoid organs and inflammation sites. Single-nucleotide polymorphisms in this gene have been associated with various diseases including immunoglobulin A nephropathy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2009]","start":169690667,"end":169711698,"strand":-1,"description":"selectin L [Source:HGNC Symbol;Acc:HGNC:10720]"}, {"versioned_ensembl_gene_id":"ENSG00000233686.3","gene_symbol":"PIEZO1P1","gene_name":"piezo type mechanosensitive ion channel component 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16214]","synonyms":"FAM38CP,C20orf83,bA164D18.1","biotype":"processed_pseudogene","ncbi_id":"128615","summary":null,"start":59460619,"end":59460837,"strand":-1,"description":"piezo type mechanosensitive ion channel component 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16214]"}, {"versioned_ensembl_gene_id":"ENSG00000230704.1","gene_symbol":"AL021940.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169762929,"end":169764648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230352.1","gene_symbol":"AL035250.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59360927,"end":59364773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171533.11","gene_symbol":"MAP6","gene_name":"microtubule associated protein 6 [Source:HGNC Symbol;Acc:HGNC:6868]","synonyms":"FLJ41346,STOP,MAP6-N,KIAA1878","biotype":"protein_coding","ncbi_id":"4135","summary":"This gene encodes a microtubule-associated protein. The encoded protein is a calmodulin-binding and calmodulin-regulated protein that is involved in microtubule stabilization. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":75586918,"end":75669120,"strand":-1,"description":"microtubule associated protein 6 [Source:HGNC Symbol;Acc:HGNC:6868]"}, {"versioned_ensembl_gene_id":"ENSG00000253472.1","gene_symbol":"AC034205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151378003,"end":151378640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211931.1","gene_symbol":"IGHD2-2","gene_name":"immunoglobulin heavy diversity 2-2 [Source:HGNC Symbol;Acc:HGNC:5490]","synonyms":"IGHD22","biotype":"IG_D_gene","ncbi_id":"28505","summary":null,"start":105916826,"end":105916856,"strand":-1,"description":"immunoglobulin heavy diversity 2-2 [Source:HGNC Symbol;Acc:HGNC:5490]"}, {"versioned_ensembl_gene_id":"ENSG00000108479.11","gene_symbol":"GALK1","gene_name":"galactokinase 1 [Source:HGNC Symbol;Acc:HGNC:4118]","synonyms":"GALK","biotype":"protein_coding","ncbi_id":"2584","summary":"Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population. [provided by RefSeq, Jul 2008]","start":75751594,"end":75765711,"strand":-1,"description":"galactokinase 1 [Source:HGNC Symbol;Acc:HGNC:4118]"}, {"versioned_ensembl_gene_id":"ENSG00000274316.1","gene_symbol":"ZNF646P1","gene_name":"zinc finger protein 646 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39749]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419854","summary":null,"start":53408882,"end":53409876,"strand":-1,"description":"zinc finger protein 646 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39749]"}, {"versioned_ensembl_gene_id":"ENSG00000231047.1","gene_symbol":"GCNT1P3","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421581","summary":null,"start":190624595,"end":190625169,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37973]"}, {"versioned_ensembl_gene_id":"ENSG00000176225.13","gene_symbol":"RTTN","gene_name":"rotatin [Source:HGNC Symbol;Acc:HGNC:18654]","synonyms":"DKFZP434G145","biotype":"protein_coding","ncbi_id":"25914","summary":"This gene encodes a large protein whose specific function is unknown. Absence of the orthologous protein in mouse results in embryonic lethality with deficient axial rotation, abnormal differentiation of the neural tube, and randomized looping of the heart tube during development. In human, mutations in this gene are associated with polymicrogyria with seizures. In human fibroblasts this protein localizes at the ciliary basal bodies. Given the intracellular localization of this protein and the phenotypic effects of mutations, this gene is suspected of playing a role in the maintenance of normal ciliary structure which in turn effects the developmental process of left-right organ specification, axial rotation, and perhaps notochord development. [provided by RefSeq, Jan 2013]","start":70003031,"end":70205945,"strand":-1,"description":"rotatin [Source:HGNC Symbol;Acc:HGNC:18654]"}, {"versioned_ensembl_gene_id":"ENSG00000229942.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29748420,"end":29748840,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000157131.10","gene_symbol":"C8A","gene_name":"complement C8 alpha chain [Source:HGNC Symbol;Acc:HGNC:1352]","synonyms":null,"biotype":"protein_coding","ncbi_id":"731","summary":"C8 is a component of the complement system and contains three polypeptides, alpha, beta and gamma. This gene encodes the alpha subunit of C8. C8 participates in the formation of the membrane attack complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in this gene cause complement C8 alpha-gamma deficiency. [provided by RefSeq, Nov 2008]","start":56854806,"end":56918221,"strand":1,"description":"complement C8 alpha chain [Source:HGNC Symbol;Acc:HGNC:1352]"}, {"versioned_ensembl_gene_id":"ENSG00000166171.12","gene_symbol":"DPCD","gene_name":"deleted in primary ciliary dyskinesia homolog (mouse) [Source:HGNC Symbol;Acc:HGNC:24542]","synonyms":"RP11-529I10.4,DKFZP566F084","biotype":"protein_coding","ncbi_id":"25911","summary":"This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia. [provided by RefSeq, Jul 2016]","start":101570560,"end":101609668,"strand":1,"description":"deleted in primary ciliary dyskinesia homolog (mouse) [Source:HGNC Symbol;Acc:HGNC:24542]"}, {"versioned_ensembl_gene_id":"ENSG00000165113.12","gene_symbol":"GKAP1","gene_name":"G kinase anchoring protein 1 [Source:HGNC Symbol;Acc:HGNC:17496]","synonyms":"GKAP42,FKSG21","biotype":"protein_coding","ncbi_id":"80318","summary":"This gene encodes a protein that is highly similar to the mouse cGMP-dependent protein kinase anchoring protein 42kDa. The mouse protein has been found to localize with the Golgi and recruit cGMP-dependent protein kinase I alpha to the Golgi in mouse testes. It is thought to play a role in germ cell development. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":83739421,"end":83829516,"strand":-1,"description":"G kinase anchoring protein 1 [Source:HGNC Symbol;Acc:HGNC:17496]"}, {"versioned_ensembl_gene_id":"ENSG00000229913.1","gene_symbol":"AL360295.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56823679,"end":56826920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197721.16","gene_symbol":"CR1L","gene_name":"complement C3b/C4b receptor 1 like [Source:HGNC Symbol;Acc:HGNC:2335]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1379","summary":null,"start":207645113,"end":207738416,"strand":1,"description":"complement C3b/C4b receptor 1 like [Source:HGNC Symbol;Acc:HGNC:2335]"}, {"versioned_ensembl_gene_id":"ENSG00000267649.1","gene_symbol":"AC010327.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55216660,"end":55221616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078304.19","gene_symbol":"PPP2R5C","gene_name":"protein phosphatase 2 regulatory subunit B'gamma [Source:HGNC Symbol;Acc:HGNC:9311]","synonyms":"PR61G,B56gamma,B56G","biotype":"protein_coding","ncbi_id":"5527","summary":"The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a gamma isoform of the regulatory subunit B56 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":101761798,"end":101927989,"strand":1,"description":"protein phosphatase 2 regulatory subunit B'gamma [Source:HGNC Symbol;Acc:HGNC:9311]"}, {"versioned_ensembl_gene_id":"ENSG00000143297.18","gene_symbol":"FCRL5","gene_name":"Fc receptor like 5 [Source:HGNC Symbol;Acc:HGNC:18508]","synonyms":"IRTA2,FCRH5,CD307e,BXMAS1","biotype":"protein_coding","ncbi_id":"83416","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and the Fc-receptor like family. This gene and several other Fc receptor-like gene members are clustered on the long arm of chromosome 1. The encoded protein is a single-pass type I membrane protein and contains 8 immunoglobulin-like C2-type domains. This gene is implicated in B cell development and lymphomagenesis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2010]","start":157513377,"end":157552520,"strand":-1,"description":"Fc receptor like 5 [Source:HGNC Symbol;Acc:HGNC:18508]"}, {"versioned_ensembl_gene_id":"ENSG00000226289.1","gene_symbol":"CDCA4P3","gene_name":"cell division cycle associated 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49772]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420558","summary":null,"start":207658454,"end":207659142,"strand":1,"description":"cell division cycle associated 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49772]"}, {"versioned_ensembl_gene_id":"ENSG00000178386.12","gene_symbol":"ZNF223","gene_name":"zinc finger protein 223 [Source:HGNC Symbol;Acc:HGNC:13016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7766","summary":"This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. The function of this protein has yet to be determined. [provided by RefSeq, Mar 2014]","start":44051367,"end":44067991,"strand":1,"description":"zinc finger protein 223 [Source:HGNC Symbol;Acc:HGNC:13016]"}, {"versioned_ensembl_gene_id":"ENSG00000150276.8","gene_symbol":"PPIAP26","gene_name":"peptidylprolyl isomerase A pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39271]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"121981","summary":null,"start":52820497,"end":52821018,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39271]"}, {"versioned_ensembl_gene_id":"ENSG00000060709.14","gene_symbol":"RIMBP2","gene_name":"RIMS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30339]","synonyms":"RIM-BP2,RBP2,PPP1R133,MGC15831,KIAA0318","biotype":"protein_coding","ncbi_id":"23504","summary":null,"start":130396137,"end":130517917,"strand":-1,"description":"RIMS binding protein 2 [Source:HGNC Symbol;Acc:HGNC:30339]"}, {"versioned_ensembl_gene_id":"ENSG00000242419.5","gene_symbol":"PCDHGC4","gene_name":"protocadherin gamma subfamily C, 4 [Source:HGNC Symbol;Acc:HGNC:8717]","synonyms":"PCDH-GAMMA-C4","biotype":"protein_coding","ncbi_id":"56098","summary":"This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]","start":141484997,"end":141512979,"strand":1,"description":"protocadherin gamma subfamily C, 4 [Source:HGNC Symbol;Acc:HGNC:8717]"}, {"versioned_ensembl_gene_id":"ENSG00000211897.9","gene_symbol":"IGHG3","gene_name":"immunoglobulin heavy constant gamma 3 (G3m marker) [Source:HGNC Symbol;Acc:HGNC:5527]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3502","summary":null,"start":105764503,"end":105771405,"strand":-1,"description":"immunoglobulin heavy constant gamma 3 (G3m marker) [Source:HGNC Symbol;Acc:HGNC:5527]"}, {"versioned_ensembl_gene_id":"ENSG00000131203.12","gene_symbol":"IDO1","gene_name":"indoleamine 2,3-dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:6059]","synonyms":"INDO,IDO","biotype":"protein_coding","ncbi_id":"3620","summary":"This gene encodes indoleamine 2,3-dioxygenase (IDO) - a heme enzyme that catalyzes the first and rate-limiting step in tryptophan catabolism to N-formyl-kynurenine. This enzyme acts on multiple tryptophan substrates including D-tryptophan, L-tryptophan, 5-hydroxy-tryptophan, tryptamine, and serotonin. This enzyme is thought to play a role in a variety of pathophysiological processes such as antimicrobial and antitumor defense, neuropathology, immunoregulation, and antioxidant activity. Through its expression in dendritic cells, monocytes, and macrophages this enzyme modulates T-cell behavior by its peri-cellular catabolization of the essential amino acid tryptophan.[provided by RefSeq, Feb 2011]","start":39902275,"end":39928444,"strand":1,"description":"indoleamine 2,3-dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:6059]"}, {"versioned_ensembl_gene_id":"ENSG00000243290.3","gene_symbol":"IGKV1-12","gene_name":"immunoglobulin kappa variable 1-12 [Source:HGNC Symbol;Acc:HGNC:5730]","synonyms":"IGKV112,L19","biotype":"IG_V_gene","ncbi_id":"28940","summary":null,"start":89040224,"end":89040745,"strand":-1,"description":"immunoglobulin kappa variable 1-12 [Source:HGNC Symbol;Acc:HGNC:5730]"}, {"versioned_ensembl_gene_id":"ENSG00000211596.3","gene_symbol":"IGKJ2","gene_name":"immunoglobulin kappa joining 2 [Source:HGNC Symbol;Acc:HGNC:5720]","synonyms":"J2","biotype":"IG_J_gene","ncbi_id":"28949","summary":null,"start":88861525,"end":88861563,"strand":-1,"description":"immunoglobulin kappa joining 2 [Source:HGNC Symbol;Acc:HGNC:5720]"}, {"versioned_ensembl_gene_id":"ENSG00000268287.1","gene_symbol":"AC008687.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49064259,"end":49064856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283270.1","gene_symbol":"AC244205.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":88811186,"end":88825207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175518.6","gene_symbol":"UBQLNL","gene_name":"ubiquilin like [Source:HGNC Symbol;Acc:HGNC:28294]","synonyms":"MGC26958,MGC20470","biotype":"protein_coding","ncbi_id":"143630","summary":null,"start":5514393,"end":5516705,"strand":-1,"description":"ubiquilin like [Source:HGNC Symbol;Acc:HGNC:28294]"}, {"versioned_ensembl_gene_id":"ENSG00000101752.11","gene_symbol":"MIB1","gene_name":"mindbomb E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21086]","synonyms":"ZZZ6,ZZANK2,MIB,KIAA1323,DIP-1","biotype":"protein_coding","ncbi_id":"57534","summary":"This gene encodes a protein containing multiple ankyrin repeats and RING finger domains that functions as an E3 ubiquitin ligase. The encoded protein positively regulates Notch signaling by ubiquitinating the Notch receptors, thereby facilitating their endocytosis. This protein may also promote the ubiquitination and degradation of death-associated protein kinase 1 (DAPK1). [provided by RefSeq, Jun 2013]","start":21704957,"end":21870957,"strand":1,"description":"mindbomb E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21086]"}, {"versioned_ensembl_gene_id":"ENSG00000189052.6","gene_symbol":"CGB5","gene_name":"chorionic gonadotropin beta subunit 5 [Source:HGNC Symbol;Acc:HGNC:16452]","synonyms":"HCG","biotype":"protein_coding","ncbi_id":"93659","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 5 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]","start":49043884,"end":49045311,"strand":1,"description":"chorionic gonadotropin beta subunit 5 [Source:HGNC Symbol;Acc:HGNC:16452]"}, {"versioned_ensembl_gene_id":"ENSG00000217648.1","gene_symbol":"AL136116.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143342246,"end":143343383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259687.1","gene_symbol":"LINC01220","gene_name":"long intergenic non-protein coding RNA 1220 [Source:HGNC Symbol;Acc:HGNC:49664]","synonyms":null,"biotype":"lincRNA","ncbi_id":"731223","summary":null,"start":75294404,"end":75296638,"strand":1,"description":"long intergenic non-protein coding RNA 1220 [Source:HGNC Symbol;Acc:HGNC:49664]"}, {"versioned_ensembl_gene_id":"ENSG00000184698.5","gene_symbol":"OR51M1","gene_name":"olfactory receptor family 51 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390059","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5383812,"end":5393263,"strand":1,"description":"olfactory receptor family 51 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14847]"}, {"versioned_ensembl_gene_id":"ENSG00000271335.5","gene_symbol":"AL117336.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35314552,"end":35336401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177303.9","gene_symbol":"CASKIN2","gene_name":"CASK interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:18200]","synonyms":"KIAA1139,FLJ21609,ANKS5B","biotype":"protein_coding","ncbi_id":"57513","summary":"This gene encodes a large protein that contains six ankyrin repeats, as well as a Src homology 3 (SH3) domain and two sterile alpha motif (SAM) domains, which may be involved in protein-protein interactions. The C-terminal portion of this protein is proline-rich and contains a conserved region. A related protein interacts with calcium/calmodulin-dependent serine protein kinase (CASK). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":75500261,"end":75515583,"strand":-1,"description":"CASK interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:18200]"}, {"versioned_ensembl_gene_id":"ENSG00000137656.11","gene_symbol":"BUD13","gene_name":"BUD13 homolog [Source:HGNC Symbol;Acc:HGNC:28199]","synonyms":"MGC13125,fSAP71,Cwc26","biotype":"protein_coding","ncbi_id":"84811","summary":null,"start":116748170,"end":116772988,"strand":-1,"description":"BUD13 homolog [Source:HGNC Symbol;Acc:HGNC:28199]"}, {"versioned_ensembl_gene_id":"ENSG00000283097.1","gene_symbol":"AL159152.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":92446470,"end":92449056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251461.3","gene_symbol":"AC091133.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49004731,"end":49013725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214178.3","gene_symbol":"PPIAP23","gene_name":"peptidylprolyl isomerase A pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39268]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390419","summary":null,"start":91272081,"end":91272577,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39268]"}, {"versioned_ensembl_gene_id":"ENSG00000254820.1","gene_symbol":"AC107882.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22113448,"end":22117001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225505.1","gene_symbol":"AC104332.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92732000,"end":92733257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236171.1","gene_symbol":"RPL12P26","gene_name":"ribosomal protein L12 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271404","summary":null,"start":117196168,"end":117196654,"strand":-1,"description":"ribosomal protein L12 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36811]"}, {"versioned_ensembl_gene_id":"ENSG00000223896.2","gene_symbol":"CCNJP2","gene_name":"cyclin J pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37997]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418724","summary":null,"start":92755794,"end":92756956,"strand":1,"description":"cyclin J pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37997]"}, {"versioned_ensembl_gene_id":"ENSG00000223787.2","gene_symbol":"AL354890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92580476,"end":92580821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253224.1","gene_symbol":"PGAM5P1","gene_name":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42467]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421133","summary":null,"start":109884610,"end":109885423,"strand":-1,"description":"PGAM family member 5, mitochondrial serine/threonine protein phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42467]"}, {"versioned_ensembl_gene_id":"ENSG00000104826.12","gene_symbol":"LHB","gene_name":"luteinizing hormone beta polypeptide [Source:HGNC Symbol;Acc:HGNC:6584]","synonyms":"LSH-B,hLHB,CGB4","biotype":"protein_coding","ncbi_id":"3972","summary":"This gene is a member of the glycoprotein hormone beta chain family and encodes the beta subunit of luteinizing hormone (LH). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. LH is expressed in the pituitary gland and promotes spermatogenesis and ovulation by stimulating the testes and ovaries to synthesize steroids. The genes for the beta chains of chorionic gonadotropin and for luteinizing hormone are contiguous on chromosome 19q13.3. Mutations in this gene are associated with hypogonadism which is characterized by infertility and pseudohermaphroditism. [provided by RefSeq, Jul 2008]","start":49015980,"end":49017081,"strand":-1,"description":"luteinizing hormone beta polypeptide [Source:HGNC Symbol;Acc:HGNC:6584]"}, {"versioned_ensembl_gene_id":"ENSG00000258354.1","gene_symbol":"AC138932.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14909887,"end":14911345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176787.2","gene_symbol":"OR52E2","gene_name":"olfactory receptor family 52 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:14769]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119678","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5058650,"end":5059627,"strand":-1,"description":"olfactory receptor family 52 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:14769]"}, {"versioned_ensembl_gene_id":"ENSG00000224337.1","gene_symbol":"FAM8A3P","gene_name":"family with sequence similarity 8 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129594","summary":null,"start":149320593,"end":149321436,"strand":1,"description":"family with sequence similarity 8 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16374]"}, {"versioned_ensembl_gene_id":"ENSG00000261593.1","gene_symbol":"CYP4A27P","gene_name":"cytochrome P450 family 4 subfamily A member 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:42414]","synonyms":"CYP4A-se3[12]","biotype":"unprocessed_pseudogene","ncbi_id":"100422288","summary":null,"start":47000898,"end":47001087,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:42414]"}, {"versioned_ensembl_gene_id":"ENSG00000272834.1","gene_symbol":"AL022238.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40415003,"end":40415445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255710.2","gene_symbol":"AP003170.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113820856,"end":113821885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250140.1","gene_symbol":"AC026801.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34860783,"end":34861506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204952.2","gene_symbol":"FBXO47","gene_name":"F-box protein 47 [Source:HGNC Symbol;Acc:HGNC:31969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"494188","summary":null,"start":38936432,"end":38967402,"strand":-1,"description":"F-box protein 47 [Source:HGNC Symbol;Acc:HGNC:31969]"}, {"versioned_ensembl_gene_id":"ENSG00000254791.1","gene_symbol":"FAR1-IT1","gene_name":"FAR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41485]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478978","summary":null,"start":13669327,"end":13670149,"strand":1,"description":"FAR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41485]"}, {"versioned_ensembl_gene_id":"ENSG00000196588.14","gene_symbol":"MKL1","gene_name":"megakaryoblastic leukemia (translocation) 1 [Source:HGNC Symbol;Acc:HGNC:14334]","synonyms":"MRTF-A,MAL,KIAA1438,BSAC","biotype":"protein_coding","ncbi_id":"57591","summary":"The protein encoded by this gene interacts with the transcription factor myocardin, a key regulator of smooth muscle cell differentiation. The encoded protein is predominantly nuclear and may help transduce signals from the cytoskeleton to the nucleus. This gene is involved in a specific translocation event that creates a fusion of this gene and the RNA-binding motif protein-15 gene. This translocation has been associated with acute megakaryocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":40410281,"end":40636702,"strand":-1,"description":"megakaryoblastic leukemia (translocation) 1 [Source:HGNC Symbol;Acc:HGNC:14334]"}, {"versioned_ensembl_gene_id":"ENSG00000229999.6","gene_symbol":"AL022238.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40372664,"end":40388290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232612.1","gene_symbol":"RPL31P35","gene_name":"ribosomal protein L31 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271199","summary":null,"start":54656358,"end":54656734,"strand":1,"description":"ribosomal protein L31 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36932]"}, {"versioned_ensembl_gene_id":"ENSG00000236107.7","gene_symbol":"AC010127.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165957399,"end":166301784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163349.21","gene_symbol":"HIPK1","gene_name":"homeodomain interacting protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:19006]","synonyms":"Nbak2,Myak,MGC33548,MGC33446,MGC26642,KIAA0630","biotype":"protein_coding","ncbi_id":"204851","summary":"The protein encoded by this gene belongs to the Ser/Thr family of protein kinases and HIPK subfamily. It phosphorylates homeodomain transcription factors and may also function as a co-repressor for homeodomain transcription factors. Alternative splicing results in four transcript variants encoding four distinct isoforms. [provided by RefSeq, Jul 2008]","start":113929192,"end":113977869,"strand":1,"description":"homeodomain interacting protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:19006]"}, {"versioned_ensembl_gene_id":"ENSG00000249621.1","gene_symbol":"AC113349.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122321291,"end":122323358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249916.1","gene_symbol":"AC119150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122369762,"end":122383568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168724.14","gene_symbol":"DNAJC21","gene_name":"DnaJ heat shock protein family (Hsp40) member C21 [Source:HGNC Symbol;Acc:HGNC:27030]","synonyms":"JJJ1,GS3,DNAJA5","biotype":"protein_coding","ncbi_id":"134218","summary":"This gene encodes a member of the DNAJ heat shock protein 40 family of proteins that is characterized by two N-terminal tetratricopeptide repeat domains and a C-terminal DNAJ domain. This protein binds the precursor 45S ribosomal RNA and may be involved in early nuclear ribosomal RNA biogenesis and maturation of the 60S ribosomal subunit. Mutations in this gene result in Bone marrow failure syndrome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2017]","start":34929593,"end":34958964,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C21 [Source:HGNC Symbol;Acc:HGNC:27030]"}, {"versioned_ensembl_gene_id":"ENSG00000234290.2","gene_symbol":"AC116366.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132468890,"end":132473043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266027.8","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31722193,"end":31747032,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000238160.1","gene_symbol":"AC116366.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132419416,"end":132426714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233926.1","gene_symbol":"AL591368.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81689713,"end":81776900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157216.15","gene_symbol":"SSBP3","gene_name":"single stranded DNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:15674]","synonyms":"SSDP1,SSDP,FLJ10355,CSDP","biotype":"protein_coding","ncbi_id":"23648","summary":null,"start":54225432,"end":54413479,"strand":-1,"description":"single stranded DNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:15674]"}, {"versioned_ensembl_gene_id":"ENSG00000074755.14","gene_symbol":"ZZEF1","gene_name":"zinc finger ZZ-type and EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29027]","synonyms":"ZZZ4,KIAA0399,FLJ10821","biotype":"protein_coding","ncbi_id":"23140","summary":null,"start":4004445,"end":4143020,"strand":-1,"description":"zinc finger ZZ-type and EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29027]"}, {"versioned_ensembl_gene_id":"ENSG00000187272.6","gene_symbol":"KRTAP9-8","gene_name":"keratin associated protein 9-8 [Source:HGNC Symbol;Acc:HGNC:17231]","synonyms":"KAP9.8","biotype":"protein_coding","ncbi_id":"83901","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41238045,"end":41239004,"strand":1,"description":"keratin associated protein 9-8 [Source:HGNC Symbol;Acc:HGNC:17231]"}, {"versioned_ensembl_gene_id":"ENSG00000260267.1","gene_symbol":"AC026471.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31456711,"end":31459736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225840.2","gene_symbol":"AC010970.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10197256,"end":10199103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228317.1","gene_symbol":"AL158070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105554035,"end":105558029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270760.1","gene_symbol":"AD001527.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36144081,"end":36148348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141965.4","gene_symbol":"FEM1A","gene_name":"fem-1 homolog A [Source:HGNC Symbol;Acc:HGNC:16934]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55527","summary":null,"start":4791681,"end":4801273,"strand":1,"description":"fem-1 homolog A [Source:HGNC Symbol;Acc:HGNC:16934]"}, {"versioned_ensembl_gene_id":"ENSG00000277543.1","gene_symbol":"AC026471.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31428180,"end":31428646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254430.1","gene_symbol":"OR6M3P","gene_name":"olfactory receptor family 6 subfamily M member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14741]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79321","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123861822,"end":123862521,"strand":-1,"description":"olfactory receptor family 6 subfamily M member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14741]"}, {"versioned_ensembl_gene_id":"ENSG00000267179.1","gene_symbol":"AC008770.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":11925075,"end":11979290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126249.7","gene_symbol":"PDCD2L","gene_name":"programmed cell death 2 like [Source:HGNC Symbol;Acc:HGNC:28194]","synonyms":"MGC13096","biotype":"protein_coding","ncbi_id":"84306","summary":null,"start":34404384,"end":34426168,"strand":1,"description":"programmed cell death 2 like [Source:HGNC Symbol;Acc:HGNC:28194]"}, {"versioned_ensembl_gene_id":"ENSG00000249738.9","gene_symbol":"AC008691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159310745,"end":159805536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260905.1","gene_symbol":"AC009021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22612543,"end":22613483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283213.1","gene_symbol":"AC130466.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22806289,"end":22813680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277297.1","gene_symbol":"ATP5A1P10","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37668]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132619","summary":null,"start":66721158,"end":66722760,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37668]"}, {"versioned_ensembl_gene_id":"ENSG00000278987.1","gene_symbol":"AL031009.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1688355,"end":1690536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257467.5","gene_symbol":"PPFIA2-AS1","gene_name":"PPFIA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53397]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724663","summary":null,"start":81270675,"end":81312422,"strand":1,"description":"PPFIA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53397]"}, {"versioned_ensembl_gene_id":"ENSG00000196365.11","gene_symbol":"LONP1","gene_name":"lon peptidase 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:9479]","synonyms":"PRSS15,PIM1,LonHS,hLON","biotype":"protein_coding","ncbi_id":"9361","summary":"This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]","start":5691834,"end":5720572,"strand":-1,"description":"lon peptidase 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:9479]"}, {"versioned_ensembl_gene_id":"ENSG00000258634.3","gene_symbol":"AL160006.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110058340,"end":110062555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204161.13","gene_symbol":"C10orf128","gene_name":"chromosome 10 open reading frame 128 [Source:HGNC Symbol;Acc:HGNC:27274]","synonyms":"Em:AC084727.5","biotype":"protein_coding","ncbi_id":"170371","summary":null,"start":49154725,"end":49188585,"strand":-1,"description":"chromosome 10 open reading frame 128 [Source:HGNC Symbol;Acc:HGNC:27274]"}, {"versioned_ensembl_gene_id":"ENSG00000278870.2","gene_symbol":"OR51G1","gene_name":"olfactory receptor family 51 subfamily G member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14738]","synonyms":"OR51G3P","biotype":"polymorphic_pseudogene","ncbi_id":"79324","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":4923374,"end":4924339,"strand":-1,"description":"olfactory receptor family 51 subfamily G member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14738]"}, {"versioned_ensembl_gene_id":"ENSG00000245812.2","gene_symbol":"LINC02202","gene_name":"long intergenic non-protein coding RNA 2202 [Source:HGNC Symbol;Acc:HGNC:53068]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927740","summary":null,"start":159100483,"end":159117478,"strand":1,"description":"long intergenic non-protein coding RNA 2202 [Source:HGNC Symbol;Acc:HGNC:53068]"}, {"versioned_ensembl_gene_id":"ENSG00000251447.1","gene_symbol":"AC107027.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131537571,"end":131537685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225541.1","gene_symbol":"AC002480.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":22571607,"end":22661792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263680.2","gene_symbol":"AC007639.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72425939,"end":72428852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264026.1","gene_symbol":"LINC02003","gene_name":"long intergenic non-protein coding RNA 2003 [Source:HGNC Symbol;Acc:HGNC:27099]","synonyms":null,"biotype":"lincRNA","ncbi_id":"146795","summary":null,"start":72342940,"end":72355136,"strand":1,"description":"long intergenic non-protein coding RNA 2003 [Source:HGNC Symbol;Acc:HGNC:27099]"}, {"versioned_ensembl_gene_id":"ENSG00000163866.8","gene_symbol":"SMIM12","gene_name":"small integral membrane protein 12 [Source:HGNC Symbol;Acc:HGNC:25154]","synonyms":"FLJ90372,C1orf212","biotype":"protein_coding","ncbi_id":"113444","summary":null,"start":34712737,"end":34859816,"strand":-1,"description":"small integral membrane protein 12 [Source:HGNC Symbol;Acc:HGNC:25154]"}, {"versioned_ensembl_gene_id":"ENSG00000227630.3","gene_symbol":"LINC01132","gene_name":"long intergenic non-protein coding RNA 1132 [Source:HGNC Symbol;Acc:HGNC:49444]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506810","summary":null,"start":234724042,"end":234736720,"strand":1,"description":"long intergenic non-protein coding RNA 1132 [Source:HGNC Symbol;Acc:HGNC:49444]"}, {"versioned_ensembl_gene_id":"ENSG00000139323.13","gene_symbol":"POC1B","gene_name":"POC1 centriolar protein B [Source:HGNC Symbol;Acc:HGNC:30836]","synonyms":"WDR51B,TUWD12,FLJ14923","biotype":"protein_coding","ncbi_id":"282809","summary":"POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutation in this gene result in autosomal-recessive cone-rod dystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":89419718,"end":89526024,"strand":-1,"description":"POC1 centriolar protein B [Source:HGNC Symbol;Acc:HGNC:30836]"}, {"versioned_ensembl_gene_id":"ENSG00000229855.8","gene_symbol":"AC008568.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121199704,"end":121357398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282179.1","gene_symbol":"TRBV7-7","gene_name":"T-cell receptor beta variable 7-7 [Source:HGNC Symbol;Acc:HGNC:12241]","synonyms":"TRBV77,TCRBV7S7,TCRBV6S6A2T","biotype":"TR_V_gene","ncbi_id":"28591","summary":null,"start":142533342,"end":142533843,"strand":1,"description":"T-cell receptor beta variable 7-7 [Source:HGNC Symbol;Acc:HGNC:12241]"}, {"versioned_ensembl_gene_id":"ENSG00000271306.1","gene_symbol":"RAC1P9","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:50774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422658","summary":null,"start":53779783,"end":53780263,"strand":1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:50774]"}, {"versioned_ensembl_gene_id":"ENSG00000228627.1","gene_symbol":"AC009468.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53559214,"end":53568249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196267.12","gene_symbol":"ZNF836","gene_name":"zinc finger protein 836 [Source:HGNC Symbol;Acc:HGNC:34333]","synonyms":"FLJ16287","biotype":"protein_coding","ncbi_id":"162962","summary":null,"start":52153864,"end":52171643,"strand":-1,"description":"zinc finger protein 836 [Source:HGNC Symbol;Acc:HGNC:34333]"}, {"versioned_ensembl_gene_id":"ENSG00000226763.4","gene_symbol":"SRRM5","gene_name":"serine/arginine repetitive matrix 5 [Source:HGNC Symbol;Acc:HGNC:37248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100170229","summary":null,"start":43596617,"end":43614497,"strand":1,"description":"serine/arginine repetitive matrix 5 [Source:HGNC Symbol;Acc:HGNC:37248]"}, {"versioned_ensembl_gene_id":"ENSG00000131116.11","gene_symbol":"ZNF428","gene_name":"zinc finger protein 428 [Source:HGNC Symbol;Acc:HGNC:20804]","synonyms":"Zfp428,MGC51082,C19orf37","biotype":"protein_coding","ncbi_id":"126299","summary":null,"start":43607219,"end":43619874,"strand":-1,"description":"zinc finger protein 428 [Source:HGNC Symbol;Acc:HGNC:20804]"}, {"versioned_ensembl_gene_id":"ENSG00000234213.1","gene_symbol":"FHP1","gene_name":"fumarate hydratase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873790","summary":null,"start":42255873,"end":42256575,"strand":1,"description":"fumarate hydratase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39442]"}, {"versioned_ensembl_gene_id":"ENSG00000256087.6","gene_symbol":"ZNF432","gene_name":"zinc finger protein 432 [Source:HGNC Symbol;Acc:HGNC:20810]","synonyms":"KIAA0798","biotype":"protein_coding","ncbi_id":"9668","summary":null,"start":52031379,"end":52095738,"strand":-1,"description":"zinc finger protein 432 [Source:HGNC Symbol;Acc:HGNC:20810]"}, {"versioned_ensembl_gene_id":"ENSG00000105048.16","gene_symbol":"TNNT1","gene_name":"troponin T1, slow skeletal type [Source:HGNC Symbol;Acc:HGNC:11948]","synonyms":"TNTS,TNT,STNT,NEM5,MGC104241,FLJ98147,ANM","biotype":"protein_coding","ncbi_id":"7138","summary":"This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":55132794,"end":55149354,"strand":-1,"description":"troponin T1, slow skeletal type [Source:HGNC Symbol;Acc:HGNC:11948]"}, {"versioned_ensembl_gene_id":"ENSG00000257645.1","gene_symbol":"AC087897.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38532895,"end":38533050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235174.1","gene_symbol":"AC019205.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73373108,"end":73373263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237788.1","gene_symbol":"AL162615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49829125,"end":49831085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223949.6","gene_symbol":"ROR1-AS1","gene_name":"ROR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40508]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927034","summary":null,"start":64094442,"end":64171297,"strand":-1,"description":"ROR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40508]"}, {"versioned_ensembl_gene_id":"ENSG00000136425.12","gene_symbol":"CIB2","gene_name":"calcium and integrin binding family member 2 [Source:HGNC Symbol;Acc:HGNC:24579]","synonyms":"USH1J,KIP2,DFNB48","biotype":"protein_coding","ncbi_id":"10518","summary":"The protein encoded by this gene is similar to that of KIP/CIB, calcineurin B, and calmodulin. The encoded protein is a calcium-binding regulatory protein that interacts with DNA-dependent protein kinase catalytic subunits (DNA-PKcs), and it is involved in photoreceptor cell maintenance. Mutations in this gene cause deafness, autosomal recessive, 48 (DFNB48), and also Usher syndrome 1J (USH1J). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":78104606,"end":78131544,"strand":-1,"description":"calcium and integrin binding family member 2 [Source:HGNC Symbol;Acc:HGNC:24579]"}, {"versioned_ensembl_gene_id":"ENSG00000231386.1","gene_symbol":"AC007395.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70810798,"end":70811474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168385.17","gene_symbol":"SEPT2","gene_name":"septin 2 [Source:HGNC Symbol;Acc:HGNC:7729]","synonyms":"Pnutl3,NEDD5,KIAA0158,hNedd5,DIFF6","biotype":"protein_coding","ncbi_id":"4735","summary":null,"start":241315100,"end":241354027,"strand":1,"description":"septin 2 [Source:HGNC Symbol;Acc:HGNC:7729]"}, {"versioned_ensembl_gene_id":"ENSG00000282134.1","gene_symbol":"TRBV6-8","gene_name":"T-cell receptor beta variable 6-8 [Source:HGNC Symbol;Acc:HGNC:12233]","synonyms":"TRBV68,TCRBV6S8,TCRBV13S7P","biotype":"TR_V_gene","ncbi_id":"28599","summary":null,"start":142529032,"end":142529526,"strand":1,"description":"T-cell receptor beta variable 6-8 [Source:HGNC Symbol;Acc:HGNC:12233]"}, {"versioned_ensembl_gene_id":"ENSG00000140678.16","gene_symbol":"ITGAX","gene_name":"integrin subunit alpha X [Source:HGNC Symbol;Acc:HGNC:6152]","synonyms":"CD11C","biotype":"protein_coding","ncbi_id":"3687","summary":"This gene encodes the integrin alpha X chain protein. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as inactivated-C3b (iC3b) receptor 4 (CR4). The alpha X beta 2 complex seems to overlap the properties of the alpha M beta 2 integrin in the adherence of neutrophils and monocytes to stimulated endothelium cells, and in the phagocytosis of complement coated particles. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":31355134,"end":31382997,"strand":1,"description":"integrin subunit alpha X [Source:HGNC Symbol;Acc:HGNC:6152]"}, {"versioned_ensembl_gene_id":"ENSG00000231868.1","gene_symbol":"AL031848.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6443034,"end":6447006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230747.1","gene_symbol":"AC021188.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96307263,"end":96321731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141748.12","gene_symbol":"ARL5C","gene_name":"ADP ribosylation factor like GTPase 5C [Source:HGNC Symbol;Acc:HGNC:31111]","synonyms":"ARL12","biotype":"protein_coding","ncbi_id":"390790","summary":null,"start":39156894,"end":39167484,"strand":-1,"description":"ADP ribosylation factor like GTPase 5C [Source:HGNC Symbol;Acc:HGNC:31111]"}, {"versioned_ensembl_gene_id":"ENSG00000196778.3","gene_symbol":"OR52K1","gene_name":"olfactory receptor family 52 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:15222]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390036","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4482646,"end":4493497,"strand":1,"description":"olfactory receptor family 52 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:15222]"}, {"versioned_ensembl_gene_id":"ENSG00000255517.6","gene_symbol":"AP002748.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66473490,"end":66480233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254916.1","gene_symbol":"AP004607.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90051837,"end":90053736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254803.1","gene_symbol":"AP004607.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90049945,"end":90050266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273367.1","gene_symbol":"AL355472.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234372186,"end":234372811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253281.6","gene_symbol":"AC092819.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":58255771,"end":58272119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233332.1","gene_symbol":"AL122008.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234212606,"end":234215088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236521.1","gene_symbol":"NPAP1P4","gene_name":"nuclear pore associated protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533674","summary":null,"start":80357029,"end":80360338,"strand":-1,"description":"nuclear pore associated protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45021]"}, {"versioned_ensembl_gene_id":"ENSG00000226565.2","gene_symbol":"AL445493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":207150205,"end":207150281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235797.2","gene_symbol":"AL160275.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114572901,"end":114573371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117595.10","gene_symbol":"IRF6","gene_name":"interferon regulatory factor 6 [Source:HGNC Symbol;Acc:HGNC:6121]","synonyms":"VWS1,VWS,OFC6,LPS","biotype":"protein_coding","ncbi_id":"3664","summary":"This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. The encoded protein may be a transcriptional activator. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. Mutations in this gene are also associated with non-syndromic orofacial cleft type 6. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2011]","start":209785623,"end":209806175,"strand":-1,"description":"interferon regulatory factor 6 [Source:HGNC Symbol;Acc:HGNC:6121]"}, {"versioned_ensembl_gene_id":"ENSG00000183092.16","gene_symbol":"BEGAIN","gene_name":"brain enriched guanylate kinase associated [Source:HGNC Symbol;Acc:HGNC:24163]","synonyms":"KIAA1446","biotype":"protein_coding","ncbi_id":"57596","summary":null,"start":100537147,"end":100587413,"strand":-1,"description":"brain enriched guanylate kinase associated [Source:HGNC Symbol;Acc:HGNC:24163]"}, {"versioned_ensembl_gene_id":"ENSG00000267110.1","gene_symbol":"AC010327.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55154757,"end":55160671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259031.1","gene_symbol":"AL845552.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100538939,"end":100540409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251296.1","gene_symbol":"AC006499.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10167159,"end":10167765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259379.1","gene_symbol":"MTND5P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:51951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075254","summary":null,"start":58152606,"end":58154407,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:51951]"}, {"versioned_ensembl_gene_id":"ENSG00000147669.10","gene_symbol":"POLR2K","gene_name":"RNA polymerase II subunit K [Source:HGNC Symbol;Acc:HGNC:9198]","synonyms":"RPB10alpha","biotype":"protein_coding","ncbi_id":"5440","summary":"This gene encodes one of the smallest subunits of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This subunit is shared by the other two DNA-directed RNA polymerases. [provided by RefSeq, Jul 2008]","start":100150584,"end":100154002,"strand":1,"description":"RNA polymerase II subunit K [Source:HGNC Symbol;Acc:HGNC:9198]"}, {"versioned_ensembl_gene_id":"ENSG00000136918.7","gene_symbol":"WDR38","gene_name":"WD repeat domain 38 [Source:HGNC Symbol;Acc:HGNC:23745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401551","summary":null,"start":124853417,"end":124857890,"strand":1,"description":"WD repeat domain 38 [Source:HGNC Symbol;Acc:HGNC:23745]"}, {"versioned_ensembl_gene_id":"ENSG00000259215.1","gene_symbol":"AC027237.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69458522,"end":69461806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262664.2","gene_symbol":"OVCA2","gene_name":"OVCA2, serine hydrolase domain containing [Source:HGNC Symbol;Acc:HGNC:24203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124641","summary":null,"start":2041936,"end":2043430,"strand":1,"description":"OVCA2, serine hydrolase domain containing [Source:HGNC Symbol;Acc:HGNC:24203]"}, {"versioned_ensembl_gene_id":"ENSG00000235652.7","gene_symbol":"AL356599.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145799409,"end":145886585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260425.1","gene_symbol":"AL031709.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1358900,"end":1361405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280184.2","gene_symbol":"AL023806.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145789270,"end":145791973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176024.17","gene_symbol":"ZNF613","gene_name":"zinc finger protein 613 [Source:HGNC Symbol;Acc:HGNC:25827]","synonyms":"FLJ13590","biotype":"protein_coding","ncbi_id":"79898","summary":null,"start":51927147,"end":51948759,"strand":1,"description":"zinc finger protein 613 [Source:HGNC Symbol;Acc:HGNC:25827]"}, {"versioned_ensembl_gene_id":"ENSG00000253603.1","gene_symbol":"CERNA3","gene_name":"competing endogenous lncRNA 3 for miR-645 [Source:HGNC Symbol;Acc:HGNC:53469]","synonyms":"CTA","biotype":"antisense_RNA","ncbi_id":"105375847","summary":null,"start":56074592,"end":56075274,"strand":1,"description":"competing endogenous lncRNA 3 for miR-645 [Source:HGNC Symbol;Acc:HGNC:53469]"}, {"versioned_ensembl_gene_id":"ENSG00000101150.17","gene_symbol":"TPD52L2","gene_name":"tumor protein D52 like 2 [Source:HGNC Symbol;Acc:HGNC:12007]","synonyms":"hD54,D54","biotype":"protein_coding","ncbi_id":"7165","summary":"This gene encodes a member of the tumor protein D52-like family. These proteins are characterized by an N-terminal coiled-coil motif that is used to form homo- and heteromeric complexes with other tumor protein D52-like proteins. Expression of this gene may be a marker for breast cancer and acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 12. [provided by RefSeq, Aug 2011]","start":63865228,"end":63891545,"strand":1,"description":"tumor protein D52 like 2 [Source:HGNC Symbol;Acc:HGNC:12007]"}, {"versioned_ensembl_gene_id":"ENSG00000260024.1","gene_symbol":"MRPS21P7","gene_name":"mitochondrial ribosomal protein S21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:29754]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359771","summary":null,"start":49708006,"end":49708243,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:29754]"}, {"versioned_ensembl_gene_id":"ENSG00000099331.13","gene_symbol":"MYO9B","gene_name":"myosin IXB [Source:HGNC Symbol;Acc:HGNC:7609]","synonyms":"CELIAC4","biotype":"protein_coding","ncbi_id":"4650","summary":"This gene encodes a member of the myosin family of actin-based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single-headed structure and exhibits processive movement on actin filaments toward the minus-end. The protein also has rho-GTPase activity. Polymorphisms in this gene are associated with celiac disease and ulcerative colitis susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":17075781,"end":17214537,"strand":1,"description":"myosin IXB [Source:HGNC Symbol;Acc:HGNC:7609]"}, {"versioned_ensembl_gene_id":"ENSG00000268056.5","gene_symbol":"AC020913.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17152588,"end":17168051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167131.16","gene_symbol":"CCDC103","gene_name":"coiled-coil domain containing 103 [Source:HGNC Symbol;Acc:HGNC:32700]","synonyms":"PR46b,FLJ34211,FLJ13094,CILD17","biotype":"protein_coding","ncbi_id":"388389","summary":"This gene encodes a protein that contains a coiled-coil domain. [provided by RefSeq, Apr 2012]","start":44899142,"end":44905390,"strand":1,"description":"coiled-coil domain containing 103 [Source:HGNC Symbol;Acc:HGNC:32700]"}, {"versioned_ensembl_gene_id":"ENSG00000278918.1","gene_symbol":"AC080112.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40348049,"end":40350539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223446.1","gene_symbol":"AL451065.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93094939,"end":93095529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237818.1","gene_symbol":"RPS3AP29","gene_name":"ribosomal protein S3a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730861","summary":null,"start":97898347,"end":97899115,"strand":-1,"description":"ribosomal protein S3a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35531]"}, {"versioned_ensembl_gene_id":"ENSG00000109851.6","gene_symbol":"DBX1","gene_name":"developing brain homeobox 1 [Source:HGNC Symbol;Acc:HGNC:33185]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120237","summary":null,"start":20156155,"end":20160613,"strand":-1,"description":"developing brain homeobox 1 [Source:HGNC Symbol;Acc:HGNC:33185]"}, {"versioned_ensembl_gene_id":"ENSG00000228379.1","gene_symbol":"AC010891.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9813315,"end":9817513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265046.1","gene_symbol":"AC004253.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31830731,"end":31831750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264699.1","gene_symbol":"LINC01912","gene_name":"long intergenic non-protein coding RNA 1912 [Source:HGNC Symbol;Acc:HGNC:52731]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372175","summary":null,"start":68258339,"end":68264827,"strand":-1,"description":"long intergenic non-protein coding RNA 1912 [Source:HGNC Symbol;Acc:HGNC:52731]"}, {"versioned_ensembl_gene_id":"ENSG00000197408.8","gene_symbol":"CYP2B6","gene_name":"cytochrome P450 family 2 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:2615]","synonyms":"CYPIIB6,CYP2B,CPB6","biotype":"protein_coding","ncbi_id":"1555","summary":"This gene, CYP2B6, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital. The enzyme is known to metabolize some xenobiotics, such as the anti-cancer drugs cyclophosphamide and ifosphamide. Transcript variants for this gene have been described; however, it has not been resolved whether these transcripts are in fact produced by this gene or by a closely related pseudogene, CYP2B7. Both the gene and the pseudogene are located in the middle of a CYP2A pseudogene found in a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. [provided by RefSeq, Jul 2008]","start":40991299,"end":41018398,"strand":1,"description":"cytochrome P450 family 2 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:2615]"}, {"versioned_ensembl_gene_id":"ENSG00000179364.13","gene_symbol":"PACS2","gene_name":"phosphofurin acidic cluster sorting protein 2 [Source:HGNC Symbol;Acc:HGNC:23794]","synonyms":"PACS1L,KIAA0602","biotype":"protein_coding","ncbi_id":"23241","summary":null,"start":105300563,"end":105398147,"strand":1,"description":"phosphofurin acidic cluster sorting protein 2 [Source:HGNC Symbol;Acc:HGNC:23794]"}, {"versioned_ensembl_gene_id":"ENSG00000221970.2","gene_symbol":"OR2A1","gene_name":"olfactory receptor family 2 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8229]","synonyms":null,"biotype":"protein_coding","ncbi_id":"346528","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144312464,"end":144322668,"strand":1,"description":"olfactory receptor family 2 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8229]"}, {"versioned_ensembl_gene_id":"ENSG00000264104.1","gene_symbol":"AC114689.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67788268,"end":67791035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272085.1","gene_symbol":"AC091979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158464465,"end":158464678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179299.16","gene_symbol":"NSUN7","gene_name":"NOP2/Sun RNA methyltransferase family member 7 [Source:HGNC Symbol;Acc:HGNC:25857]","synonyms":"FLJ14001","biotype":"protein_coding","ncbi_id":"79730","summary":null,"start":40749897,"end":40809985,"strand":1,"description":"NOP2/Sun RNA methyltransferase family member 7 [Source:HGNC Symbol;Acc:HGNC:25857]"}, {"versioned_ensembl_gene_id":"ENSG00000244479.7","gene_symbol":"OR2A1-AS1","gene_name":"OR2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49168]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928492","summary":null,"start":144300395,"end":144356181,"strand":-1,"description":"OR2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49168]"}, {"versioned_ensembl_gene_id":"ENSG00000265374.1","gene_symbol":"LINC01908","gene_name":"long intergenic non-protein coding RNA 1908 [Source:HGNC Symbol;Acc:HGNC:52727]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372037","summary":null,"start":27225742,"end":27247188,"strand":1,"description":"long intergenic non-protein coding RNA 1908 [Source:HGNC Symbol;Acc:HGNC:52727]"}, {"versioned_ensembl_gene_id":"ENSG00000284242.1","gene_symbol":"AC009452.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66278059,"end":66278664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279709.1","gene_symbol":"CU633906.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6309161,"end":6312948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180667.10","gene_symbol":"YOD1","gene_name":"YOD1 deubiquitinase [Source:HGNC Symbol;Acc:HGNC:25035]","synonyms":"OTUD2,DUBA8,DKFZp451J1719","biotype":"protein_coding","ncbi_id":"55432","summary":"Protein ubiquitination controls many intracellular processes, including cell cycle progression, transcriptional activation, and signal transduction. This dynamic process, involving ubiquitin conjugating enzymes and deubiquitinating enzymes, adds and removes ubiquitin. Deubiquitinating enzymes are cysteine proteases that specifically cleave ubiquitin from ubiquitin-conjugated protein substrates. The protein encoded by this gene belongs to a DUB subfamily characterized by an ovarian tumor (OTU) domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":207043849,"end":207052980,"strand":-1,"description":"YOD1 deubiquitinase [Source:HGNC Symbol;Acc:HGNC:25035]"}, {"versioned_ensembl_gene_id":"ENSG00000274976.1","gene_symbol":"AC087588.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32820142,"end":32820567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173674.10","gene_symbol":"EIF1AX","gene_name":"eukaryotic translation initiation factor 1A, X-linked [Source:HGNC Symbol;Acc:HGNC:3250]","synonyms":"EIF4C,EIF1A,eIF-4C,eIF-1A","biotype":"protein_coding","ncbi_id":"1964","summary":"This gene encodes an essential eukaryotic translation initiation factor. The protein is required for the binding of the 43S complex (a 40S subunit, eIF2/GTP/Met-tRNAi and eIF3) to the 5' end of capped RNA. [provided by RefSeq, Jul 2008]","start":20124518,"end":20141844,"strand":-1,"description":"eukaryotic translation initiation factor 1A, X-linked [Source:HGNC Symbol;Acc:HGNC:3250]"}, {"versioned_ensembl_gene_id":"ENSG00000237200.1","gene_symbol":"ZBTB40-IT1","gene_name":"ZBTB40 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41493]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874345","summary":null,"start":22517474,"end":22519708,"strand":1,"description":"ZBTB40 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41493]"}, {"versioned_ensembl_gene_id":"ENSG00000230534.6","gene_symbol":"AL392046.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35098006,"end":35127020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100439.10","gene_symbol":"ABHD4","gene_name":"abhydrolase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:20154]","synonyms":"FLJ12816","biotype":"protein_coding","ncbi_id":"63874","summary":null,"start":22598237,"end":22613215,"strand":1,"description":"abhydrolase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:20154]"}, {"versioned_ensembl_gene_id":"ENSG00000244331.1","gene_symbol":"AC008677.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157931258,"end":157931563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243772.7","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738515,"end":54753052,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000130595.18","gene_symbol":"TNNT3","gene_name":"troponin T3, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11950]","synonyms":"FSSV,DKFZp779M2348,DA2B,AMCD2B","biotype":"protein_coding","ncbi_id":"7140","summary":"The binding of Ca(2+) to the trimeric troponin complex initiates the process of muscle contraction. Increased Ca(2+) concentrations produce a conformational change in the troponin complex that is transmitted to tropomyosin dimers situated along actin filaments. The altered conformation permits increased interaction between a myosin head and an actin filament which, ultimately, produces a muscle contraction. The troponin complex has protein subunits C, I, and T. Subunit C binds Ca(2+) and subunit I binds to actin and inhibits actin-myosin interaction. Subunit T binds the troponin complex to the tropomyosin complex and is also required for Ca(2+)-mediated activation of actomyosin ATPase activity. There are 3 different troponin T genes that encode tissue-specific isoforms of subunit T for fast skeletal-, slow skeletal-, and cardiac-muscle. This gene encodes fast skeletal troponin T protein; also known as troponin T type 3. Alternative splicing results in multiple transcript variants encoding additional distinct troponin T type 3 isoforms. A developmentally regulated switch between fetal/neonatal and adult troponin T type 3 isoforms occurs. Additional splice variants have been described but their biological validity has not been established. Mutations in this gene may cause distal arthrogryposis multiplex congenita type 2B (DA2B). [provided by RefSeq, Oct 2009]","start":1919562,"end":1938706,"strand":1,"description":"troponin T3, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11950]"}, {"versioned_ensembl_gene_id":"ENSG00000278905.1","gene_symbol":"AC106818.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93600357,"end":93603598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110172.11","gene_symbol":"CHORDC1","gene_name":"cysteine and histidine rich domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14525]","synonyms":"CHP1,CHP-1","biotype":"protein_coding","ncbi_id":"26973","summary":null,"start":90201160,"end":90223364,"strand":-1,"description":"cysteine and histidine rich domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14525]"}, {"versioned_ensembl_gene_id":"ENSG00000159588.14","gene_symbol":"CCDC17","gene_name":"coiled-coil domain containing 17 [Source:HGNC Symbol;Acc:HGNC:26574]","synonyms":"FLJ33084","biotype":"protein_coding","ncbi_id":"149483","summary":null,"start":45620044,"end":45624057,"strand":-1,"description":"coiled-coil domain containing 17 [Source:HGNC Symbol;Acc:HGNC:26574]"}, {"versioned_ensembl_gene_id":"ENSG00000267036.2","gene_symbol":"AC005559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":590430,"end":591300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281938.1","gene_symbol":"AC026398.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":131807143,"end":131994278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218834.1","gene_symbol":"AL606923.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68598204,"end":68598393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280561.1","gene_symbol":"AL158835.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125707416,"end":125749525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260186.5","gene_symbol":"LINC02137","gene_name":"long intergenic non-protein coding RNA 2137 [Source:HGNC Symbol;Acc:HGNC:52997]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371295","summary":null,"start":58421326,"end":58462470,"strand":1,"description":"long intergenic non-protein coding RNA 2137 [Source:HGNC Symbol;Acc:HGNC:52997]"}, {"versioned_ensembl_gene_id":"ENSG00000158402.18","gene_symbol":"CDC25C","gene_name":"cell division cycle 25C [Source:HGNC Symbol;Acc:HGNC:1727]","synonyms":"PPP1R60,CDC25","biotype":"protein_coding","ncbi_id":"995","summary":"This gene encodes a conserved protein that plays a key role in the regulation of cell division. The encoded protein directs dephosphorylation of cyclin B-bound CDC2 and triggers entry into mitosis. It also suppresses p53-induced growth arrest. Multiple alternatively spliced transcript variants of this gene have been described. [provided by RefSeq, Dec 2015]","start":138285265,"end":138338355,"strand":-1,"description":"cell division cycle 25C [Source:HGNC Symbol;Acc:HGNC:1727]"}, {"versioned_ensembl_gene_id":"ENSG00000254407.1","gene_symbol":"PHBP17","gene_name":"prohibitin pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51550]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480420","summary":null,"start":123340174,"end":123340714,"strand":-1,"description":"prohibitin pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51550]"}, {"versioned_ensembl_gene_id":"ENSG00000171928.13","gene_symbol":"TVP23B","gene_name":"trans-golgi network vesicle protein 23 homolog B [Source:HGNC Symbol;Acc:HGNC:20399]","synonyms":"CGI-148,YDR084C,FAM18B1,FAM18B","biotype":"protein_coding","ncbi_id":"51030","summary":null,"start":18780995,"end":18806714,"strand":1,"description":"trans-golgi network vesicle protein 23 homolog B [Source:HGNC Symbol;Acc:HGNC:20399]"}, {"versioned_ensembl_gene_id":"ENSG00000130921.7","gene_symbol":"C12orf65","gene_name":"chromosome 12 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:26784]","synonyms":"SPG55,FLJ38663","biotype":"protein_coding","ncbi_id":"91574","summary":"This nuclear gene encodes a mitochondrial matrix protein that appears to contribute to peptide chain termination in the mitochondrial translation machinery. Two different 1 bp deletions (resulting in the same premature stop codon)result in decreased mitochondrial translation, decreased levels of oxidative phosphorylation complexes and encepthalomyopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":123232916,"end":123257959,"strand":1,"description":"chromosome 12 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:26784]"}, {"versioned_ensembl_gene_id":"ENSG00000174371.16","gene_symbol":"EXO1","gene_name":"exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3511]","synonyms":"hExoI,HEX1","biotype":"protein_coding","ncbi_id":"9156","summary":"This gene encodes a protein with 5' to 3' exonuclease activity as well as an RNase H activity. It is similar to the Saccharomyces cerevisiae protein Exo1 which interacts with Msh2 and which is involved in mismatch repair and recombination. Alternative splicing of this gene results in three transcript variants encoding two different isoforms. [provided by RefSeq, Jul 2008]","start":241847967,"end":241895148,"strand":1,"description":"exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:3511]"}, {"versioned_ensembl_gene_id":"ENSG00000211873.1","gene_symbol":"TRAJ16","gene_name":"T-cell receptor alpha joining 16 [Source:HGNC Symbol;Acc:HGNC:12044]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28739","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22528527,"end":22528586,"strand":1,"description":"T-cell receptor alpha joining 16 [Source:HGNC Symbol;Acc:HGNC:12044]"}, {"versioned_ensembl_gene_id":"ENSG00000111328.6","gene_symbol":"CDK2AP1","gene_name":"cyclin dependent kinase 2 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:14002]","synonyms":"ST19,p12DOC-1,DORC1,DOC1,doc-1","biotype":"protein_coding","ncbi_id":"8099","summary":"The protein encoded by this gene is a cyclin-dependent kinase 2 (CDK2) -associated protein which is thought to negatively regulate CDK2 activity by sequestering monomeric CDK2, and targeting CDK2 for proteolysis. This protein was found to also interact with DNA polymerase alpha/primase and mediate the phosphorylation of the large p180 subunit, which suggests a regulatory role in DNA replication during the S-phase of the cell cycle. This protein also forms a core subunit of the nucleosome remodeling and histone deacetylation (NURD) complex that epigenetically regulates embryonic stem cell differentiation. This gene thus plays a role in both cell-cycle and epigenetic regulation. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012]","start":123260971,"end":123272334,"strand":-1,"description":"cyclin dependent kinase 2 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:14002]"}, {"versioned_ensembl_gene_id":"ENSG00000240970.1","gene_symbol":"RPL23AP64","gene_name":"ribosomal protein L23a pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:36552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649946","summary":null,"start":119003012,"end":119003446,"strand":-1,"description":"ribosomal protein L23a pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:36552]"}, {"versioned_ensembl_gene_id":"ENSG00000240704.1","gene_symbol":"KLF7P1","gene_name":"kruppel like factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17207]","synonyms":"KLF7P","biotype":"processed_pseudogene","ncbi_id":"100128036","summary":null,"start":170952850,"end":170953897,"strand":-1,"description":"kruppel like factor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17207]"}, {"versioned_ensembl_gene_id":"ENSG00000259839.1","gene_symbol":"AC007614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49336683,"end":49337345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260614.1","gene_symbol":"AC007614.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49287430,"end":49290227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214676.4","gene_symbol":"AC080188.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168755816,"end":168756382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125753.13","gene_symbol":"VASP","gene_name":"vasodilator stimulated phosphoprotein [Source:HGNC Symbol;Acc:HGNC:12652]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7408","summary":"Vasodilator-stimulated phosphoprotein (VASP) is a member of the Ena-VASP protein family. Ena-VASP family members contain an EHV1 N-terminal domain that binds proteins containing E/DFPPPPXD/E motifs and targets Ena-VASP proteins to focal adhesions. In the mid-region of the protein, family members have a proline-rich domain that binds SH3 and WW domain-containing proteins. Their C-terminal EVH2 domain mediates tetramerization and binds both G and F actin. VASP is associated with filamentous actin formation and likely plays a widespread role in cell adhesion and motility. VASP may also be involved in the intracellular signaling pathways that regulate integrin-extracellular matrix interactions. VASP is regulated by the cyclic nucleotide-dependent kinases PKA and PKG. [provided by RefSeq, Jul 2008]","start":45506579,"end":45526983,"strand":1,"description":"vasodilator stimulated phosphoprotein [Source:HGNC Symbol;Acc:HGNC:12652]"}, {"versioned_ensembl_gene_id":"ENSG00000231490.1","gene_symbol":"RPL7L1P2","gene_name":"ribosomal protein L7 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420155","summary":null,"start":51259429,"end":51260167,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39484]"}, {"versioned_ensembl_gene_id":"ENSG00000152404.15","gene_symbol":"CWF19L2","gene_name":"CWF19 like 2, cell cycle control (S. pombe) [Source:HGNC Symbol;Acc:HGNC:26508]","synonyms":"FLJ32343","biotype":"protein_coding","ncbi_id":"143884","summary":null,"start":107326345,"end":107457844,"strand":-1,"description":"CWF19 like 2, cell cycle control (S. pombe) [Source:HGNC Symbol;Acc:HGNC:26508]"}, {"versioned_ensembl_gene_id":"ENSG00000275468.1","gene_symbol":"AC004678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2013728,"end":2014656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279653.1","gene_symbol":"AC004678.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2002580,"end":2003581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236044.1","gene_symbol":"FABP5P2","gene_name":"fatty acid binding protein 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31060]","synonyms":"FABP5L2","biotype":"processed_pseudogene","ncbi_id":"729163","summary":null,"start":51966742,"end":51967149,"strand":1,"description":"fatty acid binding protein 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31060]"}, {"versioned_ensembl_gene_id":"ENSG00000279697.1","gene_symbol":"AP003400.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89545128,"end":89545744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271454.1","gene_symbol":"AL353729.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39159071,"end":39160319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196878.14","gene_symbol":"LAMB3","gene_name":"laminin subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:6490]","synonyms":"nicein-125kDa,LAMNB1,kalinin-140kDa,BM600-125kDa","biotype":"protein_coding","ncbi_id":"3914","summary":"The product encoded by this gene is a laminin that belongs to a family of basement membrane proteins. This protein is a beta subunit laminin, which together with an alpha and a gamma subunit, forms laminin-5. Mutations in this gene cause epidermolysis bullosa junctional Herlitz type, and generalized atrophic benign epidermolysis bullosa, diseases that are characterized by blistering of the skin. Multiple alternatively spliced transcript variants that encode the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":209614870,"end":209652466,"strand":-1,"description":"laminin subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:6490]"}, {"versioned_ensembl_gene_id":"ENSG00000135749.18","gene_symbol":"PCNX2","gene_name":"pecanex homolog 2 [Source:HGNC Symbol;Acc:HGNC:8736]","synonyms":"PCNXL2,KIAA0435,FLJ11383","biotype":"protein_coding","ncbi_id":"80003","summary":"This gene contains coding mononucleotide repeats that are associated with tumors of high mcrosatellite instability (MSI-H). Defects in this gene are involved in the tumorigenesis of MSI-H colorectal carcinomas. [provided by RefSeq, Jun 2016]","start":232983435,"end":233295713,"strand":-1,"description":"pecanex homolog 2 [Source:HGNC Symbol;Acc:HGNC:8736]"}, {"versioned_ensembl_gene_id":"ENSG00000272186.1","gene_symbol":"AP003392.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119067374,"end":119067698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136824.18","gene_symbol":"SMC2","gene_name":"structural maintenance of chromosomes 2 [Source:HGNC Symbol;Acc:HGNC:14011]","synonyms":"SMC2L1,hCAP-E,CAP-E","biotype":"protein_coding","ncbi_id":"10592","summary":null,"start":104094260,"end":104141417,"strand":1,"description":"structural maintenance of chromosomes 2 [Source:HGNC Symbol;Acc:HGNC:14011]"}, {"versioned_ensembl_gene_id":"ENSG00000259096.1","gene_symbol":"FAM35CP","gene_name":"family with sequence similarity 35 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31427]","synonyms":"FAM35AP,FAM35A2","biotype":"processed_pseudogene","ncbi_id":"100128781","summary":null,"start":87952527,"end":87955203,"strand":1,"description":"family with sequence similarity 35 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:31427]"}, {"versioned_ensembl_gene_id":"ENSG00000105996.6","gene_symbol":"HOXA2","gene_name":"homeobox A2 [Source:HGNC Symbol;Acc:HGNC:5103]","synonyms":"HOX1K","biotype":"protein_coding","ncbi_id":"3199","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. The encoded protein may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development. [provided by RefSeq, Jul 2008]","start":27100354,"end":27102811,"strand":-1,"description":"homeobox A2 [Source:HGNC Symbol;Acc:HGNC:5103]"}, {"versioned_ensembl_gene_id":"ENSG00000269993.1","gene_symbol":"KC877982.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151182386,"end":151182855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171049.8","gene_symbol":"FPR2","gene_name":"formyl peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:3827]","synonyms":"FPRH2,FPR2A,FMLPX,FMLP-R-II,ALXR,LXA4R,HM63,FPRL1","biotype":"protein_coding","ncbi_id":"2358","summary":null,"start":51752026,"end":51770526,"strand":1,"description":"formyl peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:3827]"}, {"versioned_ensembl_gene_id":"ENSG00000129993.14","gene_symbol":"CBFA2T3","gene_name":"CBFA2/RUNX1 translocation partner 3 [Source:HGNC Symbol;Acc:HGNC:1537]","synonyms":"ZMYND4,RUNX1T3,MTGR2,MTG16,ETO2","biotype":"protein_coding","ncbi_id":"863","summary":"This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(16;21)(q24;q22) translocation is one of the less common karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. This gene is also a putative breast tumor suppressor. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010]","start":88874858,"end":88977204,"strand":-1,"description":"CBFA2/RUNX1 translocation partner 3 [Source:HGNC Symbol;Acc:HGNC:1537]"}, {"versioned_ensembl_gene_id":"ENSG00000256453.1","gene_symbol":"DND1","gene_name":"DND microRNA-mediated repression inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:23799]","synonyms":"RBMS4,MGC34750","biotype":"protein_coding","ncbi_id":"373863","summary":"This gene encodes a protein that binds to microRNA-targeting sequences of mRNAs, inhibiting microRNA-mediated repression. Reduced expression of this gene has been implicated in tongue squamous cell carcinoma. Two pseudogenes of this gene are located on the long arm of chromosome 17. [provided by RefSeq, Dec 2010]","start":140670794,"end":140673586,"strand":-1,"description":"DND microRNA-mediated repression inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:23799]"}, {"versioned_ensembl_gene_id":"ENSG00000237892.1","gene_symbol":"KLF7-IT1","gene_name":"KLF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41355]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874272","summary":null,"start":207120884,"end":207122044,"strand":-1,"description":"KLF7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41355]"}, {"versioned_ensembl_gene_id":"ENSG00000223575.2","gene_symbol":"RBMX2P3","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421047","summary":null,"start":119084998,"end":119085954,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39925]"}, {"versioned_ensembl_gene_id":"ENSG00000224238.2","gene_symbol":"WARS2-IT1","gene_name":"WARS2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41393]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104472716","summary":null,"start":119047405,"end":119064785,"strand":1,"description":"WARS2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41393]"}, {"versioned_ensembl_gene_id":"ENSG00000227712.1","gene_symbol":"AL359915.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119260265,"end":119327303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224826.1","gene_symbol":"AC019109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224169664,"end":224171537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187984.12","gene_symbol":"ANKRD19P","gene_name":"ankyrin repeat domain 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:22567]","synonyms":"FLJ36178,ANKRD19","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"138649","summary":null,"start":92809388,"end":92888693,"strand":1,"description":"ankyrin repeat domain 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:22567]"}, {"versioned_ensembl_gene_id":"ENSG00000211840.1","gene_symbol":"TRAJ49","gene_name":"T-cell receptor alpha joining 49 [Source:HGNC Symbol;Acc:HGNC:12080]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28706","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22489488,"end":22489543,"strand":1,"description":"T-cell receptor alpha joining 49 [Source:HGNC Symbol;Acc:HGNC:12080]"}, {"versioned_ensembl_gene_id":"ENSG00000267534.2","gene_symbol":"S1PR2","gene_name":"sphingosine-1-phosphate receptor 2 [Source:HGNC Symbol;Acc:HGNC:3169]","synonyms":"H218,Gpcr13,EDG5,DFNB68,AGR16","biotype":"protein_coding","ncbi_id":"9294","summary":"This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]","start":10221435,"end":10231272,"strand":-1,"description":"sphingosine-1-phosphate receptor 2 [Source:HGNC Symbol;Acc:HGNC:3169]"}, {"versioned_ensembl_gene_id":"ENSG00000148835.10","gene_symbol":"TAF5","gene_name":"TATA-box binding protein associated factor 5 [Source:HGNC Symbol;Acc:HGNC:11539]","synonyms":"TAFII100,TAF2D","biotype":"protein_coding","ncbi_id":"6877","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes an integral subunit of TFIID associated with all transcriptionally competent forms of that complex. This subunit interacts strongly with two TFIID subunits that show similarity to histones H3 and H4, and it may participate in forming a nucleosome-like core in the TFIID complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":103367967,"end":103389065,"strand":1,"description":"TATA-box binding protein associated factor 5 [Source:HGNC Symbol;Acc:HGNC:11539]"}, {"versioned_ensembl_gene_id":"ENSG00000177946.5","gene_symbol":"CENPBD1","gene_name":"CENPB DNA-binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28272]","synonyms":"MGC16385","biotype":"protein_coding","ncbi_id":"92806","summary":null,"start":89969791,"end":89972534,"strand":-1,"description":"CENPB DNA-binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28272]"}, {"versioned_ensembl_gene_id":"ENSG00000162139.9","gene_symbol":"NEU3","gene_name":"neuraminidase 3 [Source:HGNC Symbol;Acc:HGNC:7760]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10825","summary":"This gene product belongs to a family of glycohydrolytic enzymes which remove sialic acid residues from glycoproteins and glycolipids. It is localized in the plasma membrane, and its activity is specific for gangliosides. It may play a role in modulating the ganglioside content of the lipid bilayer. [provided by RefSeq, Jul 2008]","start":74988134,"end":75018893,"strand":1,"description":"neuraminidase 3 [Source:HGNC Symbol;Acc:HGNC:7760]"}, {"versioned_ensembl_gene_id":"ENSG00000258536.1","gene_symbol":"FKBP1BP1","gene_name":"FK506 binding protein 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107984636","summary":null,"start":41742639,"end":41742963,"strand":1,"description":"FK506 binding protein 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52378]"}, {"versioned_ensembl_gene_id":"ENSG00000224222.1","gene_symbol":"AC024601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69994626,"end":70007836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238048.1","gene_symbol":"ART2P","gene_name":"ADP-ribosyltransferase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:724]","synonyms":"ART1P,RT6","biotype":"unprocessed_pseudogene","ncbi_id":"418","summary":null,"start":72519986,"end":72521733,"strand":1,"description":"ADP-ribosyltransferase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:724]"}, {"versioned_ensembl_gene_id":"ENSG00000228397.2","gene_symbol":"LINC01635","gene_name":"long intergenic non-protein coding RNA 1635 [Source:HGNC Symbol;Acc:HGNC:52422]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928043","summary":null,"start":22023990,"end":22026048,"strand":-1,"description":"long intergenic non-protein coding RNA 1635 [Source:HGNC Symbol;Acc:HGNC:52422]"}, {"versioned_ensembl_gene_id":"ENSG00000235893.5","gene_symbol":"BX284632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65816932,"end":65817472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239253.1","gene_symbol":"RPS4XP23","gene_name":"ribosomal protein S4X pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:48367]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480153","summary":null,"start":34021659,"end":34021895,"strand":1,"description":"ribosomal protein S4X pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:48367]"}, {"versioned_ensembl_gene_id":"ENSG00000183385.9","gene_symbol":"TTTY8","gene_name":"testis-specific transcript, Y-linked 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18489]","synonyms":"TTY8,NCRNA00130,LINC00130","biotype":"lincRNA","ncbi_id":"84673","summary":null,"start":9691100,"end":9693957,"strand":1,"description":"testis-specific transcript, Y-linked 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18489]"}, {"versioned_ensembl_gene_id":"ENSG00000258549.1","gene_symbol":"AL161713.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83805496,"end":83805640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226285.1","gene_symbol":"NUP35P2","gene_name":"nucleoporin 35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101059916","summary":null,"start":79543911,"end":79544853,"strand":-1,"description":"nucleoporin 35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52371]"}, {"versioned_ensembl_gene_id":"ENSG00000235907.2","gene_symbol":"AC115285.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33512008,"end":33512743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274914.4","gene_symbol":"LILRA5","gene_name":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]","synonyms":"LIR9,CD85,LILRB7,ILT11,CD85f","biotype":"protein_coding","ncbi_id":"353514","summary":"The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":54314131,"end":54327636,"strand":-1,"description":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]"}, {"versioned_ensembl_gene_id":"ENSG00000277835.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54830630,"end":54842447,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000226147.1","gene_symbol":"TUBBP10","gene_name":"tubulin beta class I pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418902","summary":null,"start":52994726,"end":52996026,"strand":1,"description":"tubulin beta class I pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42344]"}, {"versioned_ensembl_gene_id":"ENSG00000237279.2","gene_symbol":"AC099677.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52943536,"end":52943930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123191.14","gene_symbol":"ATP7B","gene_name":"ATPase copper transporting beta [Source:HGNC Symbol;Acc:HGNC:870]","synonyms":"WND","biotype":"protein_coding","ncbi_id":"540","summary":"This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein is a monomer, and functions as a copper-transporting ATPase which exports copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease which is characterized by copper accumulation. [provided by RefSeq, Dec 2019]","start":51930436,"end":52012125,"strand":-1,"description":"ATPase copper transporting beta [Source:HGNC Symbol;Acc:HGNC:870]"}, {"versioned_ensembl_gene_id":"ENSG00000279775.1","gene_symbol":"AC004585.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40597113,"end":40598585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110801.13","gene_symbol":"PSMD9","gene_name":"proteasome 26S subunit, non-ATPase 9 [Source:HGNC Symbol;Acc:HGNC:9567]","synonyms":"Rpn4,p27","biotype":"protein_coding","ncbi_id":"5715","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":121888731,"end":121918297,"strand":1,"description":"proteasome 26S subunit, non-ATPase 9 [Source:HGNC Symbol;Acc:HGNC:9567]"}, {"versioned_ensembl_gene_id":"ENSG00000206077.10","gene_symbol":"ZDHHC11B","gene_name":"zinc finger DHHC-type containing 11B [Source:HGNC Symbol;Acc:HGNC:32962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653082","summary":null,"start":710360,"end":766952,"strand":-1,"description":"zinc finger DHHC-type containing 11B [Source:HGNC Symbol;Acc:HGNC:32962]"}, {"versioned_ensembl_gene_id":"ENSG00000250464.1","gene_symbol":"LRRC34P2","gene_name":"leucine rich repeat containing 34 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420613","summary":null,"start":55313011,"end":55313924,"strand":-1,"description":"leucine rich repeat containing 34 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49888]"}, {"versioned_ensembl_gene_id":"ENSG00000107651.12","gene_symbol":"SEC23IP","gene_name":"SEC23 interacting protein [Source:HGNC Symbol;Acc:HGNC:17018]","synonyms":"p125","biotype":"protein_coding","ncbi_id":"11196","summary":"This gene encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]","start":119892711,"end":119944658,"strand":1,"description":"SEC23 interacting protein [Source:HGNC Symbol;Acc:HGNC:17018]"}, {"versioned_ensembl_gene_id":"ENSG00000229323.1","gene_symbol":"DLEU1-AS1","gene_name":"DLEU1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50496]","synonyms":"LINC01308","biotype":"lincRNA","ncbi_id":"103689915","summary":null,"start":50520933,"end":50527449,"strand":-1,"description":"DLEU1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50496]"}, {"versioned_ensembl_gene_id":"ENSG00000273559.4","gene_symbol":"CWC25","gene_name":"CWC25 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:25989]","synonyms":"FLJ20291,CCDC49","biotype":"protein_coding","ncbi_id":"54883","summary":"This gene encodes a factor that is part of the multi-protein C complex involved in pre-mRNA splicing. Alternatively spliced transcripts have been described for this gene. [provided by RefSeq, Nov 2012]","start":38800434,"end":38825481,"strand":-1,"description":"CWC25 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:25989]"}, {"versioned_ensembl_gene_id":"ENSG00000233700.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"Em:AB014080.3,TMPOL1","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30511094,"end":30512636,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000242578.1","gene_symbol":"AC073288.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170410512,"end":170418615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272446.5","gene_symbol":"AL158850.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":139159157,"end":139277181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144935.14","gene_symbol":"TRPC1","gene_name":"transient receptor potential cation channel subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:12333]","synonyms":"HTRP-1","biotype":"protein_coding","ncbi_id":"7220","summary":"The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":142724074,"end":142807888,"strand":1,"description":"transient receptor potential cation channel subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:12333]"}, {"versioned_ensembl_gene_id":"ENSG00000260060.1","gene_symbol":"AC009088.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31196131,"end":31196963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279689.1","gene_symbol":"AC022400.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73769264,"end":73772862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186940.6","gene_symbol":"CHCHD2P9","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23676]","synonyms":"CHCHD9,C9orf49","biotype":"processed_pseudogene","ncbi_id":"645345","summary":null,"start":79391304,"end":79391759,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23676]"}, {"versioned_ensembl_gene_id":"ENSG00000211818.1","gene_symbol":"TRAV39","gene_name":"T-cell receptor alpha variable 39 [Source:HGNC Symbol;Acc:HGNC:12139]","synonyms":"TCRAV27S1,TCRAV39S1","biotype":"TR_V_gene","ncbi_id":"28642","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22304054,"end":22304553,"strand":1,"description":"T-cell receptor alpha variable 39 [Source:HGNC Symbol;Acc:HGNC:12139]"}, {"versioned_ensembl_gene_id":"ENSG00000119681.11","gene_symbol":"LTBP2","gene_name":"latent transforming growth factor beta binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6715]","synonyms":"LTBP3,C14orf141","biotype":"protein_coding","ncbi_id":"4053","summary":"The protein encoded by this gene belongs to the family of latent transforming growth factor (TGF)-beta binding proteins (LTBP), which are extracellular matrix proteins with multi-domain structure. This protein is the largest member of the LTBP family possessing unique regions and with most similarity to the fibrillins. It has thus been suggested that it may have multiple functions: as a member of the TGF-beta latent complex, as a structural component of microfibrils, and a role in cell adhesion. [provided by RefSeq, Jul 2008]","start":74498170,"end":74612378,"strand":-1,"description":"latent transforming growth factor beta binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6715]"}, {"versioned_ensembl_gene_id":"ENSG00000255422.1","gene_symbol":"AP002954.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118704607,"end":118750263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277143.1","gene_symbol":"AC074276.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158336430,"end":158336777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250677.1","gene_symbol":"AC114781.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83237303,"end":83237444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227333.8","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"C6orf30,G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31861940,"end":31879868,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000231659.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30407752,"end":30408920,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000228766.3","gene_symbol":"RPL7L1P8","gene_name":"ribosomal protein L7 like 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39490]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402152","summary":null,"start":182610674,"end":182611414,"strand":1,"description":"ribosomal protein L7 like 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39490]"}, {"versioned_ensembl_gene_id":"ENSG00000232189.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"OTTHUMG00000086663,BPG126D10.10","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577415,"end":29577704,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000214643.6","gene_symbol":"DEFB133","gene_name":"defensin beta 133 [Source:HGNC Symbol;Acc:HGNC:31331]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403339","summary":null,"start":49946021,"end":49950265,"strand":-1,"description":"defensin beta 133 [Source:HGNC Symbol;Acc:HGNC:31331]"}, {"versioned_ensembl_gene_id":"ENSG00000249669.9","gene_symbol":"CARMN","gene_name":"cardiac mesoderm enhancer-associated non-coding RNA [Source:HGNC Symbol;Acc:HGNC:42872]","synonyms":"MIR143HG,CARMEN","biotype":"lincRNA","ncbi_id":"728264","summary":null,"start":149406689,"end":149432835,"strand":1,"description":"cardiac mesoderm enhancer-associated non-coding RNA [Source:HGNC Symbol;Acc:HGNC:42872]"}, {"versioned_ensembl_gene_id":"ENSG00000274214.1","gene_symbol":"AP005212.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14253548,"end":14254075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273713.2","gene_symbol":"TAS2R9","gene_name":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]","synonyms":"TRB6,T2R9","biotype":"protein_coding","ncbi_id":"50835","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10809137,"end":10810168,"strand":-1,"description":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]"}, {"versioned_ensembl_gene_id":"ENSG00000236401.1","gene_symbol":"SLC4A1APP2","gene_name":"solute carrier family 4 member 1 adaptor protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49812]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422527","summary":null,"start":187706561,"end":187708898,"strand":1,"description":"solute carrier family 4 member 1 adaptor protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49812]"}, {"versioned_ensembl_gene_id":"ENSG00000244213.1","gene_symbol":"ZFAND6P1","gene_name":"zinc finger AN1-type containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631382","summary":null,"start":35449748,"end":35450352,"strand":1,"description":"zinc finger AN1-type containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42978]"}, {"versioned_ensembl_gene_id":"ENSG00000254721.1","gene_symbol":"AP000879.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70206291,"end":70207390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268731.1","gene_symbol":"AC010615.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21381220,"end":21381921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261716.1","gene_symbol":"AC239868.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":149844498,"end":149849024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226996.5","gene_symbol":"AP000477.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24043257,"end":24050286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237257.1","gene_symbol":"MTND2P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42109]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873178","summary":null,"start":78741720,"end":78742744,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42109]"}, {"versioned_ensembl_gene_id":"ENSG00000274397.1","gene_symbol":"AL357153.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70556206,"end":70557478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270287.1","gene_symbol":"AL359704.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":226411615,"end":226412135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277182.1","gene_symbol":"AC006449.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38749360,"end":38751457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257390.5","gene_symbol":"AC023055.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55757275,"end":55827546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116711.9","gene_symbol":"PLA2G4A","gene_name":"phospholipase A2 group IVA [Source:HGNC Symbol;Acc:HGNC:9035]","synonyms":"PLA2G4,cPLA2-alpha","biotype":"protein_coding","ncbi_id":"5321","summary":"This gene encodes a member of the cytosolic phospholipase A2 group IV family. The enzyme catalyzes the hydrolysis of membrane phospholipids to release arachidonic acid which is subsequently metabolized into eicosanoids. Eicosanoids, including prostaglandins and leukotrienes, are lipid-based cellular hormones that regulate hemodynamics, inflammatory responses, and other intracellular pathways. The hydrolysis reaction also produces lysophospholipids that are converted into platelet-activating factor. The enzyme is activated by increased intracellular Ca(2+) levels and phosphorylation, resulting in its translocation from the cytosol and nucleus to perinuclear membrane vesicles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":186828953,"end":186988981,"strand":1,"description":"phospholipase A2 group IVA [Source:HGNC Symbol;Acc:HGNC:9035]"}, {"versioned_ensembl_gene_id":"ENSG00000254542.1","gene_symbol":"NAV2-AS3","gene_name":"NAV2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40742]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874013","summary":null,"start":19978699,"end":19981337,"strand":-1,"description":"NAV2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40742]"}, {"versioned_ensembl_gene_id":"ENSG00000254453.1","gene_symbol":"NAV2-AS2","gene_name":"NAV2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40743]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874014","summary":null,"start":20043846,"end":20049303,"strand":-1,"description":"NAV2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40743]"}, {"versioned_ensembl_gene_id":"ENSG00000219451.3","gene_symbol":"RPL23P8","gene_name":"ribosomal protein L23 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36225]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"222901","summary":null,"start":20827326,"end":20827753,"strand":1,"description":"ribosomal protein L23 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36225]"}, {"versioned_ensembl_gene_id":"ENSG00000276592.1","gene_symbol":"PHBP6","gene_name":"prohibitin pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39285]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478940","summary":null,"start":75203926,"end":75204711,"strand":1,"description":"prohibitin pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39285]"}, {"versioned_ensembl_gene_id":"ENSG00000263829.1","gene_symbol":"FAM60BP","gene_name":"family with sequence similarity 60 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:19052]","synonyms":"HsT2323","biotype":"processed_pseudogene","ncbi_id":"100421588","summary":null,"start":26255698,"end":26256355,"strand":-1,"description":"family with sequence similarity 60 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:19052]"}, {"versioned_ensembl_gene_id":"ENSG00000177602.5","gene_symbol":"HASPIN","gene_name":"histone H3 associated protein kinase [Source:HGNC Symbol;Acc:HGNC:19682]","synonyms":"GSG2","biotype":"protein_coding","ncbi_id":"83903","summary":null,"start":3723903,"end":3726699,"strand":1,"description":"histone H3 associated protein kinase [Source:HGNC Symbol;Acc:HGNC:19682]"}, {"versioned_ensembl_gene_id":"ENSG00000187806.7","gene_symbol":"TMEM202","gene_name":"transmembrane protein 202 [Source:HGNC Symbol;Acc:HGNC:33733]","synonyms":"FLJ27523","biotype":"protein_coding","ncbi_id":"338949","summary":null,"start":72398273,"end":72408029,"strand":1,"description":"transmembrane protein 202 [Source:HGNC Symbol;Acc:HGNC:33733]"}, {"versioned_ensembl_gene_id":"ENSG00000261856.1","gene_symbol":"LINC02186","gene_name":"long intergenic non-protein coding RNA 2186 [Source:HGNC Symbol;Acc:HGNC:53048]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927348","summary":null,"start":14018880,"end":14021077,"strand":-1,"description":"long intergenic non-protein coding RNA 2186 [Source:HGNC Symbol;Acc:HGNC:53048]"}, {"versioned_ensembl_gene_id":"ENSG00000187815.9","gene_symbol":"ZFP69","gene_name":"ZFP69 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:24708]","synonyms":"ZSCAN54A,ZNF642,ZKSCAN23A,ZFP69A,FLJ16030","biotype":"protein_coding","ncbi_id":"339559","summary":null,"start":40477215,"end":40496343,"strand":1,"description":"ZFP69 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:24708]"}, {"versioned_ensembl_gene_id":"ENSG00000235773.8","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30677910,"end":30681283,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000225274.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"dJ271M21.8,PsiGPR53","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537638,"end":29538721,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000270379.5","gene_symbol":"HEATR9","gene_name":"HEAT repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:26548]","synonyms":"FLJ32830,C17orf66","biotype":"protein_coding","ncbi_id":"256957","summary":null,"start":35854946,"end":35868891,"strand":-1,"description":"HEAT repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:26548]"}, {"versioned_ensembl_gene_id":"ENSG00000214456.8","gene_symbol":"PLIN5","gene_name":"perilipin 5 [Source:HGNC Symbol;Acc:HGNC:33196]","synonyms":"LSDP5,LSDA5,OXPAT,MLDP","biotype":"protein_coding","ncbi_id":"440503","summary":"Members of the perilipin family, such as PLIN5, coat intracellular lipid storage droplets and protect them from lipolytic degradation (Dalen et al., 2007 [PubMed 17234449]).[supplied by OMIM, Feb 2010]","start":4522531,"end":4535224,"strand":-1,"description":"perilipin 5 [Source:HGNC Symbol;Acc:HGNC:33196]"}, {"versioned_ensembl_gene_id":"ENSG00000260874.5","gene_symbol":"AC106820.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2456252,"end":2459979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138073.13","gene_symbol":"PREB","gene_name":"prolactin regulatory element binding [Source:HGNC Symbol;Acc:HGNC:9356]","synonyms":"SEC12","biotype":"protein_coding","ncbi_id":"10113","summary":"This gene encodes a protein that specifically binds to a Pit1-binding element of the prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand. [provided by RefSeq, Jul 2008]","start":27130756,"end":27134675,"strand":-1,"description":"prolactin regulatory element binding [Source:HGNC Symbol;Acc:HGNC:9356]"}, {"versioned_ensembl_gene_id":"ENSG00000165816.12","gene_symbol":"VWA2","gene_name":"von Willebrand factor A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24709]","synonyms":"CCSP-2,AMACO,NET42,FLJ45857,FLJ16213","biotype":"protein_coding","ncbi_id":"340706","summary":"This gene encodes a member of the von Willebrand factor A-like domain protein superfamily. The encoded protein is localized to the extracellular matrix and may serve as a structural component in basement membranes or in anchoring structures on scaffolds of collagen VII or fibrillin. This gene has been linked to type 1A diabetes and is a candidate serological marker for colon cancer. [provided by RefSeq, Jan 2013]","start":114239330,"end":114291513,"strand":1,"description":"von Willebrand factor A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24709]"}, {"versioned_ensembl_gene_id":"ENSG00000233107.1","gene_symbol":"SUCLA2P2","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38102]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129863","summary":null,"start":76106016,"end":76107324,"strand":-1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38102]"}, {"versioned_ensembl_gene_id":"ENSG00000230690.1","gene_symbol":"AC013402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104659337,"end":104664837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140284.10","gene_symbol":"SLC27A2","gene_name":"solute carrier family 27 member 2 [Source:HGNC Symbol;Acc:HGNC:10996]","synonyms":"VLCS,VLACS,HsT17226,hFACVL1,FATP2,FACVL1,ACSVL1","biotype":"protein_coding","ncbi_id":"11001","summary":"The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]","start":50182196,"end":50236395,"strand":1,"description":"solute carrier family 27 member 2 [Source:HGNC Symbol;Acc:HGNC:10996]"}, {"versioned_ensembl_gene_id":"ENSG00000282624.1","gene_symbol":"TRBV3-1","gene_name":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]","synonyms":"TRBV31,TCRBV9S1A1T,TCRBV3S1","biotype":"TR_V_gene","ncbi_id":"28619","summary":null,"start":142308565,"end":142309071,"strand":1,"description":"T-cell receptor beta variable 3-1 [Source:HGNC Symbol;Acc:HGNC:12212]"}, {"versioned_ensembl_gene_id":"ENSG00000185760.15","gene_symbol":"KCNQ5","gene_name":"potassium voltage-gated channel subfamily Q member 5 [Source:HGNC Symbol;Acc:HGNC:6299]","synonyms":"Kv7.5","biotype":"protein_coding","ncbi_id":"56479","summary":"This gene is a member of the KCNQ potassium channel gene family that is differentially expressed in subregions of the brain and in skeletal muscle. The protein encoded by this gene yields currents that activate slowly with depolarization and can form heteromeric channels with the protein encoded by the KCNQ3 gene. Currents expressed from this protein have voltage dependences and inhibitor sensitivities in common with M-currents. They are also inhibited by M1 muscarinic receptor activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":72621792,"end":73198851,"strand":1,"description":"potassium voltage-gated channel subfamily Q member 5 [Source:HGNC Symbol;Acc:HGNC:6299]"}, {"versioned_ensembl_gene_id":"ENSG00000214064.3","gene_symbol":"RPL6P5","gene_name":"ribosomal protein L6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36199]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270844","summary":null,"start":145337230,"end":145338057,"strand":1,"description":"ribosomal protein L6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36199]"}, {"versioned_ensembl_gene_id":"ENSG00000269356.1","gene_symbol":"AL356740.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113008778,"end":113009424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235280.2","gene_symbol":"MCF2L-AS1","gene_name":"MCF2L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39825]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289410","summary":null,"start":112967484,"end":112968824,"strand":-1,"description":"MCF2L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39825]"}, {"versioned_ensembl_gene_id":"ENSG00000234156.1","gene_symbol":"AL162254.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122609915,"end":122639685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104313.17","gene_symbol":"EYA1","gene_name":"EYA transcriptional coactivator and phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3519]","synonyms":"BOR","biotype":"protein_coding","ncbi_id":"2138","summary":"This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2013]","start":71197433,"end":71362232,"strand":-1,"description":"EYA transcriptional coactivator and phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3519]"}, {"versioned_ensembl_gene_id":"ENSG00000242208.1","gene_symbol":"RPL5P29","gene_name":"ribosomal protein L5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36335]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390158","summary":null,"start":56357328,"end":56358221,"strand":1,"description":"ribosomal protein L5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36335]"}, {"versioned_ensembl_gene_id":"ENSG00000271434.3","gene_symbol":"AL445237.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":124447152,"end":124450048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218029.3","gene_symbol":"AL078601.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79354443,"end":79354713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279127.1","gene_symbol":"AL121950.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49721931,"end":49724007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113504.20","gene_symbol":"SLC12A7","gene_name":"solute carrier family 12 member 7 [Source:HGNC Symbol;Acc:HGNC:10915]","synonyms":"KCC4,DKFZP434F076","biotype":"protein_coding","ncbi_id":"10723","summary":null,"start":1050376,"end":1112035,"strand":-1,"description":"solute carrier family 12 member 7 [Source:HGNC Symbol;Acc:HGNC:10915]"}, {"versioned_ensembl_gene_id":"ENSG00000237106.2","gene_symbol":"FABP5P15","gene_name":"fatty acid binding protein 5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:31071]","synonyms":"FABP5L15","biotype":"processed_pseudogene","ncbi_id":"100873958","summary":null,"start":77727867,"end":77728080,"strand":1,"description":"fatty acid binding protein 5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:31071]"}, {"versioned_ensembl_gene_id":"ENSG00000172602.9","gene_symbol":"RND1","gene_name":"Rho family GTPase 1 [Source:HGNC Symbol;Acc:HGNC:18314]","synonyms":"RHOS,Rho6,ARHS","biotype":"protein_coding","ncbi_id":"27289","summary":"This gene encodes a protein that belongs to the Rho GTPase family. Members of this family regulate the organization of the actin cytoskeleton in response to extracellular growth factors. A similar protein in rat interacts with a microtubule regulator to control axon extension. [provided by RefSeq, Apr 2014]","start":48857145,"end":48865898,"strand":-1,"description":"Rho family GTPase 1 [Source:HGNC Symbol;Acc:HGNC:18314]"}, {"versioned_ensembl_gene_id":"ENSG00000238064.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33419923,"end":33425374,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000169371.13","gene_symbol":"SNUPN","gene_name":"snurportin 1 [Source:HGNC Symbol;Acc:HGNC:14245]","synonyms":"Snurportin1,SNURPORTIN-1,RNUT1","biotype":"protein_coding","ncbi_id":"10073","summary":"The nuclear import of the spliceosomal snRNPs U1, U2, U4 and U5, is dependent on the presence of a complex nuclear localization signal. The latter is composed of the 5'-2,2,7-terminal trimethylguanosine (m3G) cap structure of the U snRNA and the Sm core domain. The protein encoded by this gene interacts specifically with m3G-cap and functions as an snRNP-specific nuclear import receptor. Alternatively spliced transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":75598083,"end":75626469,"strand":-1,"description":"snurportin 1 [Source:HGNC Symbol;Acc:HGNC:14245]"}, {"versioned_ensembl_gene_id":"ENSG00000250436.1","gene_symbol":"LINC02499","gene_name":"long intergenic non-protein coding RNA 2499 [Source:HGNC Symbol;Acc:HGNC:53484]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728040","summary":null,"start":73508803,"end":73534128,"strand":1,"description":"long intergenic non-protein coding RNA 2499 [Source:HGNC Symbol;Acc:HGNC:53484]"}, {"versioned_ensembl_gene_id":"ENSG00000203999.8","gene_symbol":"LINC01270","gene_name":"long intergenic non-protein coding RNA 1270 [Source:HGNC Symbol;Acc:HGNC:27658]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284751","summary":null,"start":50292720,"end":50314922,"strand":1,"description":"long intergenic non-protein coding RNA 1270 [Source:HGNC Symbol;Acc:HGNC:27658]"}, {"versioned_ensembl_gene_id":"ENSG00000272087.1","gene_symbol":"AC080013.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158693120,"end":158693768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173517.10","gene_symbol":"PEAK1","gene_name":"pseudopodium enriched atypical kinase 1 [Source:HGNC Symbol;Acc:HGNC:29431]","synonyms":"sgk269,KIAA2002","biotype":"protein_coding","ncbi_id":"79834","summary":"This gene encodes a non-receptor tyrosine kinase that is a member of the new kinase family three (NFK3) family. In migrating cells, the encoded protein is associated with the actin cytoskeleton and focal adhesions and promotes developing focal adhesion elongation. This protein may play a role in the regulation of cell migration, proliferation and cancer metastasis. [provided by RefSeq, Mar 2014]","start":77100656,"end":77420144,"strand":-1,"description":"pseudopodium enriched atypical kinase 1 [Source:HGNC Symbol;Acc:HGNC:29431]"}, {"versioned_ensembl_gene_id":"ENSG00000142798.17","gene_symbol":"HSPG2","gene_name":"heparan sulfate proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:5273]","synonyms":"SJS1,PRCAN,perlecan","biotype":"protein_coding","ncbi_id":"3339","summary":"This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans (heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and transthyretin, etc., and it plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and tardive dyskinesia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]","start":21822245,"end":21937297,"strand":-1,"description":"heparan sulfate proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:5273]"}, {"versioned_ensembl_gene_id":"ENSG00000262267.5","gene_symbol":"U95743.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13730137,"end":13779760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230086.1","gene_symbol":"VN1R96P","gene_name":"vomeronasal 1 receptor 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:37416]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100127969","summary":null,"start":40121311,"end":40122168,"strand":-1,"description":"vomeronasal 1 receptor 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:37416]"}, {"versioned_ensembl_gene_id":"ENSG00000259648.1","gene_symbol":"AL132640.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":67614929,"end":67616626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242022.8","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29373478,"end":29450027,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000224533.4","gene_symbol":"TMLHE-AS1","gene_name":"TMLHE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44261]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507404","summary":null,"start":155466540,"end":155611616,"strand":1,"description":"TMLHE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44261]"}, {"versioned_ensembl_gene_id":"ENSG00000196832.4","gene_symbol":"OR11G2","gene_name":"olfactory receptor family 11 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15346]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390439","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20190894,"end":20201075,"strand":1,"description":"olfactory receptor family 11 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15346]"}, {"versioned_ensembl_gene_id":"ENSG00000091640.7","gene_symbol":"SPAG7","gene_name":"sperm associated antigen 7 [Source:HGNC Symbol;Acc:HGNC:11216]","synonyms":"MGC20134,FSA-1,ACRP","biotype":"protein_coding","ncbi_id":"9552","summary":null,"start":4959226,"end":4967872,"strand":-1,"description":"sperm associated antigen 7 [Source:HGNC Symbol;Acc:HGNC:11216]"}, {"versioned_ensembl_gene_id":"ENSG00000238151.1","gene_symbol":"MLLT10P1","gene_name":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15794]","synonyms":"MLLT10L,bA348I14.3","biotype":"processed_pseudogene","ncbi_id":"140678","summary":null,"start":30403123,"end":30403384,"strand":-1,"description":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15794]"}, {"versioned_ensembl_gene_id":"ENSG00000231707.4","gene_symbol":"PABPC1P1","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8558]","synonyms":"PABPCP1,PABP1","biotype":"processed_pseudogene","ncbi_id":"26980","summary":null,"start":39973444,"end":39974338,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8558]"}, {"versioned_ensembl_gene_id":"ENSG00000039560.13","gene_symbol":"RAI14","gene_name":"retinoic acid induced 14 [Source:HGNC Symbol;Acc:HGNC:14873]","synonyms":"RAI13,KIAA1334,NORPEG,DKFZp564G013","biotype":"protein_coding","ncbi_id":"26064","summary":null,"start":34656237,"end":34832627,"strand":1,"description":"retinoic acid induced 14 [Source:HGNC Symbol;Acc:HGNC:14873]"}, {"versioned_ensembl_gene_id":"ENSG00000198721.12","gene_symbol":"ECI2","gene_name":"enoyl-CoA delta isomerase 2 [Source:HGNC Symbol;Acc:HGNC:14601]","synonyms":"PECI,HCA88,DRS1,ACBD2","biotype":"protein_coding","ncbi_id":"10455","summary":"This gene encodes a member of the hydratase/isomerase superfamily. The protein encoded is a key mitochondrial enzyme involved in beta-oxidation of unsaturated fatty acids. It catalyzes the transformation of 3-cis and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-, mono-, and polyunsaturated fatty acids to the 2-trans-enoyl-CoA intermediates. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011]","start":4115689,"end":4135597,"strand":-1,"description":"enoyl-CoA delta isomerase 2 [Source:HGNC Symbol;Acc:HGNC:14601]"}, {"versioned_ensembl_gene_id":"ENSG00000259388.1","gene_symbol":"AC025040.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49794246,"end":49796097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277375.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRY,KIRZ,KIR15,KIR2DL6","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754958,"end":54767824,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000258185.2","gene_symbol":"AC010196.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86599578,"end":86838998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272542.1","gene_symbol":"AL137246.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102888858,"end":102889834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257897.1","gene_symbol":"AC139697.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86015697,"end":86016441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272440.1","gene_symbol":"AC080013.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158695367,"end":158695581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224397.5","gene_symbol":"SMIM25","gene_name":"small integral membrane protein 25 [Source:HGNC Symbol;Acc:HGNC:50328]","synonyms":"LINC01272","biotype":"lincRNA","ncbi_id":"100506115","summary":null,"start":50267486,"end":50279795,"strand":1,"description":"small integral membrane protein 25 [Source:HGNC Symbol;Acc:HGNC:50328]"}, {"versioned_ensembl_gene_id":"ENSG00000253506.2","gene_symbol":"NACA2","gene_name":"nascent polypeptide associated complex alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:23290]","synonyms":"NACAL,MGC71999","biotype":"protein_coding","ncbi_id":"342538","summary":null,"start":61590426,"end":61591202,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:23290]"}, {"versioned_ensembl_gene_id":"ENSG00000181761.5","gene_symbol":"OR8H3","gene_name":"olfactory receptor family 8 subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:15309]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390152","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56122373,"end":56123311,"strand":1,"description":"olfactory receptor family 8 subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:15309]"}, {"versioned_ensembl_gene_id":"ENSG00000274826.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000254511.1","gene_symbol":"AP002802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81970994,"end":81987813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169488.6","gene_symbol":"OR4K15","gene_name":"olfactory receptor family 4 subfamily K member 15 [Source:HGNC Symbol;Acc:HGNC:15353]","synonyms":"OR4K15Q","biotype":"protein_coding","ncbi_id":"81127","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19975444,"end":19976659,"strand":1,"description":"olfactory receptor family 4 subfamily K member 15 [Source:HGNC Symbol;Acc:HGNC:15353]"}, {"versioned_ensembl_gene_id":"ENSG00000260871.1","gene_symbol":"AC093510.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":90388468,"end":90389363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270878.1","gene_symbol":"AL136038.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63594031,"end":63595291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233514.1","gene_symbol":"AL356653.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44122153,"end":44122512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266818.1","gene_symbol":"AP005901.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15254418,"end":15271744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226359.1","gene_symbol":"ACTG1P24","gene_name":"actin gamma 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49661]","synonyms":"POTENP","biotype":"processed_pseudogene","ncbi_id":"441783","summary":null,"start":17242010,"end":17242886,"strand":1,"description":"actin gamma 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49661]"}, {"versioned_ensembl_gene_id":"ENSG00000228781.1","gene_symbol":"AL353705.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78180214,"end":78180693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087470.17","gene_symbol":"DNM1L","gene_name":"dynamin 1 like [Source:HGNC Symbol;Acc:HGNC:2973]","synonyms":"VPS1,HDYNIV,DYMPLE,DVLP,DRP1","biotype":"protein_coding","ncbi_id":"10059","summary":"This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]","start":32679200,"end":32745650,"strand":1,"description":"dynamin 1 like [Source:HGNC Symbol;Acc:HGNC:2973]"}, {"versioned_ensembl_gene_id":"ENSG00000224859.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"RPA12,HTEX-6,tctex-6,hZR14","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30048795,"end":30054799,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000233068.2","gene_symbol":"AL590004.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3893126,"end":3894292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161149.12","gene_symbol":"TUBA3FP","gene_name":"tubulin alpha 3f pseudogene [Source:HGNC Symbol;Acc:HGNC:24067]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"113691","summary":null,"start":21008193,"end":21014292,"strand":-1,"description":"tubulin alpha 3f pseudogene [Source:HGNC Symbol;Acc:HGNC:24067]"}, {"versioned_ensembl_gene_id":"ENSG00000204700.5","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"hs6M1-6,dJ80I19.4,OR6-8","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29170907,"end":29175811,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000138829.11","gene_symbol":"FBN2","gene_name":"fibrillin 2 [Source:HGNC Symbol;Acc:HGNC:3604]","synonyms":"DA9,CCA","biotype":"protein_coding","ncbi_id":"2201","summary":"The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]","start":128257909,"end":128659185,"strand":-1,"description":"fibrillin 2 [Source:HGNC Symbol;Acc:HGNC:3604]"}, {"versioned_ensembl_gene_id":"ENSG00000238286.1","gene_symbol":"SLC35E1P1","gene_name":"solute carrier family 35 member E1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42046]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727991","summary":null,"start":20607268,"end":20608131,"strand":1,"description":"solute carrier family 35 member E1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42046]"}, {"versioned_ensembl_gene_id":"ENSG00000250831.1","gene_symbol":"AC074131.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89466537,"end":89470039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249057.1","gene_symbol":"MAST4-IT1","gene_name":"MAST4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41448]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874310","summary":null,"start":66662331,"end":66662988,"strand":1,"description":"MAST4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41448]"}, {"versioned_ensembl_gene_id":"ENSG00000100726.14","gene_symbol":"TELO2","gene_name":"telomere maintenance 2 [Source:HGNC Symbol;Acc:HGNC:29099]","synonyms":"TEL2,KIAA0683,hCLK2","biotype":"protein_coding","ncbi_id":"9894","summary":"This gene encodes a protein that functions as an S-phase checkpoint protein in the cell cycle. The protein may also play a role in DNA repair.[provided by RefSeq, Mar 2009]","start":1493344,"end":1510457,"strand":1,"description":"telomere maintenance 2 [Source:HGNC Symbol;Acc:HGNC:29099]"}, {"versioned_ensembl_gene_id":"ENSG00000269403.1","gene_symbol":"AC008750.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":51350373,"end":51368099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234825.3","gene_symbol":"XRCC6P2","gene_name":"X-ray repair cross complementing 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45184]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389901","summary":null,"start":150231075,"end":150232896,"strand":-1,"description":"X-ray repair cross complementing 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45184]"}, {"versioned_ensembl_gene_id":"ENSG00000253380.1","gene_symbol":"AC090155.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49496763,"end":49512180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260630.6","gene_symbol":"SNAI3-AS1","gene_name":"SNAI3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28327]","synonyms":"MGC23284","biotype":"antisense_RNA","ncbi_id":"197187","summary":null,"start":88663298,"end":88687186,"strand":1,"description":"SNAI3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28327]"}, {"versioned_ensembl_gene_id":"ENSG00000012660.13","gene_symbol":"ELOVL5","gene_name":"ELOVL fatty acid elongase 5 [Source:HGNC Symbol;Acc:HGNC:21308]","synonyms":"dJ483K16.1,SCA38,HELO1","biotype":"protein_coding","ncbi_id":"60481","summary":"This gene belongs to the ELO family. It is highly expressed in the adrenal gland and testis, and encodes a multi-pass membrane protein that is localized in the endoplasmic reticulum. This protein is involved in the elongation of long-chain polyunsaturated fatty acids. Mutations in this gene have been associated with spinocerebellar ataxia-38 (SCA38). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":53267398,"end":53349179,"strand":-1,"description":"ELOVL fatty acid elongase 5 [Source:HGNC Symbol;Acc:HGNC:21308]"}, {"versioned_ensembl_gene_id":"ENSG00000198934.4","gene_symbol":"MAGEE1","gene_name":"MAGE family member E1 [Source:HGNC Symbol;Acc:HGNC:24934]","synonyms":"KIAA1587,DAMAGE","biotype":"protein_coding","ncbi_id":"57692","summary":"This gene encodes an alpha-dystrobrevin-associated MAGE (melanoma-associated antigen) protein, which is a member of the MAGE family. The protein contains a nuclear localization signal in the N-terminus, 30 12-amino acid repeats beginning at nt 60 with the consensus sequence ASEGPSTSVLPT, and two MAGE domains in the C-terminus. It may play a signaling role in brain, muscle, and peripheral nerve. This gene is located on X chromosome in a region containing loci linked to cognitive disability. [provided by RefSeq, Mar 2010]","start":76427724,"end":76431353,"strand":1,"description":"MAGE family member E1 [Source:HGNC Symbol;Acc:HGNC:24934]"}, {"versioned_ensembl_gene_id":"ENSG00000225062.1","gene_symbol":"CATIP-AS1","gene_name":"CATIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41080]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101928513","summary":null,"start":218366665,"end":218367835,"strand":-1,"description":"CATIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41080]"}, {"versioned_ensembl_gene_id":"ENSG00000259150.5","gene_symbol":"LINC00929","gene_name":"long intergenic non-protein coding RNA 929 [Source:HGNC Symbol;Acc:HGNC:48615]","synonyms":null,"biotype":"lincRNA","ncbi_id":"503519","summary":null,"start":26115813,"end":26133037,"strand":1,"description":"long intergenic non-protein coding RNA 929 [Source:HGNC Symbol;Acc:HGNC:48615]"}, {"versioned_ensembl_gene_id":"ENSG00000264668.1","gene_symbol":"AC138696.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":143247110,"end":143276403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219102.3","gene_symbol":"HNRNPA3P12","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48758]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421395","summary":null,"start":53974969,"end":53976031,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48758]"}, {"versioned_ensembl_gene_id":"ENSG00000249803.5","gene_symbol":"AC112178.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136466677,"end":136520298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260284.1","gene_symbol":"TPSP2","gene_name":"tryptase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14136]","synonyms":"Mastin","biotype":"unprocessed_pseudogene","ncbi_id":"650474","summary":null,"start":1286351,"end":1288837,"strand":-1,"description":"tryptase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14136]"}, {"versioned_ensembl_gene_id":"ENSG00000166477.12","gene_symbol":"LEO1","gene_name":"LEO1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:30401]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123169","summary":"LEO1, parafibromin (CDC73; MIM 607393), CTR9 (MIM 609366), and PAF1 (MIM 610506) form the PAF protein complex that associates with the RNA polymerase II subunit POLR2A (MIM 180660) and with a histone methyltransferase complex (Rozenblatt-Rosen et al., 2005 [PubMed 15632063]).[supplied by OMIM, Mar 2008]","start":51938025,"end":51971806,"strand":-1,"description":"LEO1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:30401]"}, {"versioned_ensembl_gene_id":"ENSG00000259185.1","gene_symbol":"AC090971.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51908902,"end":51909642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171603.16","gene_symbol":"CLSTN1","gene_name":"calsyntenin 1 [Source:HGNC Symbol;Acc:HGNC:17447]","synonyms":"CSTN1,CDHR12,KIAA0911","biotype":"protein_coding","ncbi_id":"22883","summary":"This gene is a member of the calsyntenin family, a subset of the cadherin superfamily. The encoded transmembrane protein, also known as alcadein-alpha, is thought to bind to kinesin-1 motors to mediate the axonal anterograde transport of certain types of vesicle. Amyloid precursor protein (APP) is trafficked via these vesicles and so this protein is being investigated to see how it might contribute to the mechanisms underlying Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":9729026,"end":9824526,"strand":-1,"description":"calsyntenin 1 [Source:HGNC Symbol;Acc:HGNC:17447]"}, {"versioned_ensembl_gene_id":"ENSG00000164053.19","gene_symbol":"ATRIP","gene_name":"ATR interacting protein [Source:HGNC Symbol;Acc:HGNC:33499]","synonyms":"MGC21482,FLJ12343,MGC20625,MGC26740","biotype":"protein_coding","ncbi_id":"84126","summary":"This gene encodes an essential component of the DNA damage checkpoint. The encoded protein binds to single-stranded DNA coated with replication protein A. The protein also interacts with the ataxia telangiectasia and Rad3 related protein kinase, resulting in its accumulation at intranuclear foci induced by DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2012]","start":48446710,"end":48465716,"strand":1,"description":"ATR interacting protein [Source:HGNC Symbol;Acc:HGNC:33499]"}, {"versioned_ensembl_gene_id":"ENSG00000237139.1","gene_symbol":"RPS26P41","gene_name":"ribosomal protein S26 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271567","summary":null,"start":73537803,"end":73538391,"strand":1,"description":"ribosomal protein S26 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36062]"}, {"versioned_ensembl_gene_id":"ENSG00000212994.5","gene_symbol":"RPS26P6","gene_name":"ribosomal protein S26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31090]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392256","summary":null,"start":100895771,"end":100896118,"strand":1,"description":"ribosomal protein S26 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31090]"}, {"versioned_ensembl_gene_id":"ENSG00000227402.11","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"KE4,D6S2244E,ZIP7,HKE4,RING5,H2-KE4","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33354325,"end":33358319,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000270193.1","gene_symbol":"AC009237.12","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95616492,"end":95617233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226854.1","gene_symbol":"AL451105.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75903105,"end":75904858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225005.1","gene_symbol":"AC211485.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73314107,"end":73315213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282772.1","gene_symbol":"AL358790.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102845761,"end":102854513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251286.2","gene_symbol":"AC097522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52440494,"end":52441535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227053.1","gene_symbol":"AC105446.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101014320,"end":101017608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230428.1","gene_symbol":"AL049542.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":451404,"end":453461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233026.1","gene_symbol":"MTCO1P5","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51300]","synonyms":"AC026166.2-001","biotype":"processed_pseudogene","ncbi_id":"106480318","summary":null,"start":12165299,"end":12165642,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51300]"}, {"versioned_ensembl_gene_id":"ENSG00000269072.1","gene_symbol":"AC063977.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51152923,"end":51181966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226247.1","gene_symbol":"SUPT4H1P1","gene_name":"SPT4 homolog, DSIF elongation factor subunit pseudogene [Source:HGNC Symbol;Acc:HGNC:33981]","synonyms":"SUPT4H1P","biotype":"processed_pseudogene","ncbi_id":"100190947","summary":null,"start":75651288,"end":75651627,"strand":-1,"description":"SPT4 homolog, DSIF elongation factor subunit pseudogene [Source:HGNC Symbol;Acc:HGNC:33981]"}, {"versioned_ensembl_gene_id":"ENSG00000132746.14","gene_symbol":"ALDH3B2","gene_name":"aldehyde dehydrogenase 3 family member B2 [Source:HGNC Symbol;Acc:HGNC:411]","synonyms":"ALDH8","biotype":"protein_coding","ncbi_id":"222","summary":"This gene encodes a member of the aldehyde dehydrogenase family, a group of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The gene of this particular family member is over 10 kb in length. Altered methylation patterns at this locus have been observed in spermatozoa derived from patients exhibiting reduced fecundity. [provided by RefSeq, Aug 2017]","start":67662162,"end":67681200,"strand":-1,"description":"aldehyde dehydrogenase 3 family member B2 [Source:HGNC Symbol;Acc:HGNC:411]"}, {"versioned_ensembl_gene_id":"ENSG00000254889.1","gene_symbol":"AC084121.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7696830,"end":7697093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231861.2","gene_symbol":"OR5K2","gene_name":"olfactory receptor family 5 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14774]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402135","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98497604,"end":98498663,"strand":1,"description":"olfactory receptor family 5 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14774]"}, {"versioned_ensembl_gene_id":"ENSG00000234324.1","gene_symbol":"AC005517.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15443639,"end":15444191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220600.2","gene_symbol":"AL121834.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":138878899,"end":138879407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224992.2","gene_symbol":"AL445645.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":132768965,"end":132770212,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165698.15","gene_symbol":"SPACA9","gene_name":"sperm acrosome associated 9 [Source:HGNC Symbol;Acc:HGNC:1367]","synonyms":"Mast,C9orf9","biotype":"protein_coding","ncbi_id":"11092","summary":null,"start":132878027,"end":132890201,"strand":1,"description":"sperm acrosome associated 9 [Source:HGNC Symbol;Acc:HGNC:1367]"}, {"versioned_ensembl_gene_id":"ENSG00000180658.4","gene_symbol":"OR2A4","gene_name":"olfactory receptor family 2 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14729]","synonyms":"OR2A10","biotype":"protein_coding","ncbi_id":"79541","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131699644,"end":131701401,"strand":-1,"description":"olfactory receptor family 2 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14729]"}, {"versioned_ensembl_gene_id":"ENSG00000273237.1","gene_symbol":"AC004520.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26173533,"end":26174945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175182.14","gene_symbol":"FAM131A","gene_name":"family with sequence similarity 131 member A [Source:HGNC Symbol;Acc:HGNC:28308]","synonyms":"MGC21688,C3orf40","biotype":"protein_coding","ncbi_id":"131408","summary":null,"start":184335926,"end":184348421,"strand":1,"description":"family with sequence similarity 131 member A [Source:HGNC Symbol;Acc:HGNC:28308]"}, {"versioned_ensembl_gene_id":"ENSG00000110047.17","gene_symbol":"EHD1","gene_name":"EH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:3242]","synonyms":"PAST1,HPAST1,H-PAST,FLJ44618,FLJ42622","biotype":"protein_coding","ncbi_id":"10938","summary":"This gene belongs to a highly conserved gene family encoding EPS15 homology (EH) domain-containing proteins. The protein-binding EH domain was first noted in EPS15, a substrate for the epidermal growth factor receptor. The EH domain has been shown to be an important motif in proteins involved in protein-protein interactions and in intracellular sorting. The protein encoded by this gene is thought to play a role in the endocytosis of IGF1 receptors. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]","start":64851642,"end":64888296,"strand":-1,"description":"EH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:3242]"}, {"versioned_ensembl_gene_id":"ENSG00000161021.12","gene_symbol":"MAML1","gene_name":"mastermind like transcriptional coactivator 1 [Source:HGNC Symbol;Acc:HGNC:13632]","synonyms":"Mam-1,KIAA0200","biotype":"protein_coding","ncbi_id":"9794","summary":"This protein is the human homolog of mastermind, a Drosophila protein that plays a role in the Notch signaling pathway involved in cell-fate determination. There is in vitro evidence that the human homolog forms a complex with the intracellular portion of human Notch receptors and can increase expression of a Notch-induced gene. This evidence supports its proposed function as a transcriptional co-activator in the Notch signaling pathway. [provided by RefSeq, Jul 2008]","start":179732850,"end":179777286,"strand":1,"description":"mastermind like transcriptional coactivator 1 [Source:HGNC Symbol;Acc:HGNC:13632]"}, {"versioned_ensembl_gene_id":"ENSG00000064115.10","gene_symbol":"TM7SF3","gene_name":"transmembrane 7 superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:23049]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51768","summary":null,"start":26973195,"end":27014434,"strand":-1,"description":"transmembrane 7 superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:23049]"}, {"versioned_ensembl_gene_id":"ENSG00000272368.2","gene_symbol":"AC074032.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50112197,"end":50165618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267073.1","gene_symbol":"AC005256.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1748056,"end":1748745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186442.7","gene_symbol":"KRT3","gene_name":"keratin 3 [Source:HGNC Symbol;Acc:HGNC:6440]","synonyms":"K3,CK3","biotype":"protein_coding","ncbi_id":"3850","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52789685,"end":52796117,"strand":-1,"description":"keratin 3 [Source:HGNC Symbol;Acc:HGNC:6440]"}, {"versioned_ensembl_gene_id":"ENSG00000243939.1","gene_symbol":"AC090142.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104981164,"end":104981579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267275.1","gene_symbol":"AC020911.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16283359,"end":16324514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185247.14","gene_symbol":"MAGEA11","gene_name":"MAGE family member A11 [Source:HGNC Symbol;Acc:HGNC:6798]","synonyms":"CT1.11,MGC10511,MAGEA-11,MAGE11,MAGE-11","biotype":"protein_coding","ncbi_id":"4110","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":149688228,"end":149717266,"strand":1,"description":"MAGE family member A11 [Source:HGNC Symbol;Acc:HGNC:6798]"}, {"versioned_ensembl_gene_id":"ENSG00000242675.1","gene_symbol":"RPS16P9","gene_name":"ribosomal protein S16 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35659]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645412","summary":null,"start":45332698,"end":45333124,"strand":-1,"description":"ribosomal protein S16 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35659]"}, {"versioned_ensembl_gene_id":"ENSG00000227854.1","gene_symbol":"AL590135.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":239052748,"end":239052903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138835.22","gene_symbol":"RGS3","gene_name":"regulator of G protein signaling 3 [Source:HGNC Symbol;Acc:HGNC:9999]","synonyms":"PDZ-RGS3,FLJ20370,C2PA","biotype":"protein_coding","ncbi_id":"5998","summary":"This gene encodes a member of the regulator of G-protein signaling (RGS) family. This protein is a GTPase-activating protein that inhibits G-protein-mediated signal transduction. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different isoforms. Long isoforms are largely cytosolic and plasma membrane-associated with a function in Wnt signaling and in the epithelial mesenchymal transition, while shorter N-terminally-truncated isoforms can be nuclear. [provided by RefSeq, Jan 2013]","start":113444731,"end":113597743,"strand":1,"description":"regulator of G protein signaling 3 [Source:HGNC Symbol;Acc:HGNC:9999]"}, {"versioned_ensembl_gene_id":"ENSG00000224783.1","gene_symbol":"MIPEPP2","gene_name":"mitochondrial intermediate peptidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130099","summary":null,"start":238777049,"end":238779200,"strand":-1,"description":"mitochondrial intermediate peptidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39457]"}, {"versioned_ensembl_gene_id":"ENSG00000225997.1","gene_symbol":"OR4A8","gene_name":"olfactory receptor family 4 subfamily A member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15165]","synonyms":"OR4A8P","biotype":"polymorphic_pseudogene","ncbi_id":"81315","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":54682877,"end":54683821,"strand":1,"description":"olfactory receptor family 4 subfamily A member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15165]"}, {"versioned_ensembl_gene_id":"ENSG00000175319.3","gene_symbol":"NF1P5","gene_name":"neurofibromin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:7770]","synonyms":"NF1L5","biotype":"processed_pseudogene","ncbi_id":"4768","summary":null,"start":14153001,"end":14157342,"strand":-1,"description":"neurofibromin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:7770]"}, {"versioned_ensembl_gene_id":"ENSG00000198056.13","gene_symbol":"PRIM1","gene_name":"primase (DNA) subunit 1 [Source:HGNC Symbol;Acc:HGNC:9369]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5557","summary":"The replication of DNA in eukaryotic cells is carried out by a complex chromosomal replication apparatus, in which DNA polymerase alpha and primase are two key enzymatic components. Primase, which is a heterodimer of a small subunit and a large subunit, synthesizes small RNA primers for the Okazaki fragments made during discontinuous DNA replication. The protein encoded by this gene is the small, 49 kDa primase subunit. [provided by RefSeq, Jul 2008]","start":56731596,"end":56752373,"strand":-1,"description":"primase (DNA) subunit 1 [Source:HGNC Symbol;Acc:HGNC:9369]"}, {"versioned_ensembl_gene_id":"ENSG00000262543.1","gene_symbol":"SMIM28","gene_name":"small integral membrane protein 28 [Source:HGNC Symbol;Acc:HGNC:53434]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":138377905,"end":138383075,"strand":1,"description":"small integral membrane protein 28 [Source:HGNC Symbol;Acc:HGNC:53434]"}, {"versioned_ensembl_gene_id":"ENSG00000119862.12","gene_symbol":"LGALSL","gene_name":"galectin like [Source:HGNC Symbol;Acc:HGNC:25012]","synonyms":"HSPC159,GRP","biotype":"protein_coding","ncbi_id":"29094","summary":null,"start":64453969,"end":64461381,"strand":1,"description":"galectin like [Source:HGNC Symbol;Acc:HGNC:25012]"}, {"versioned_ensembl_gene_id":"ENSG00000197575.6","gene_symbol":"RPS17P2","gene_name":"ribosomal protein S17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10398]","synonyms":"RPS17L1,RPS17A","biotype":"processed_pseudogene","ncbi_id":"6219","summary":null,"start":116716243,"end":116716650,"strand":1,"description":"ribosomal protein S17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10398]"}, {"versioned_ensembl_gene_id":"ENSG00000254840.1","gene_symbol":"AC024405.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50307681,"end":50361706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280665.1","gene_symbol":"AL513210.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":168820423,"end":168820656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266647.1","gene_symbol":"AC053481.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62260634,"end":62261936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278694.1","gene_symbol":"AL354980.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154312462,"end":154313084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230993.1","gene_symbol":"RPL12P15","gene_name":"ribosomal protein L12 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36619]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270920","summary":null,"start":121658475,"end":121658973,"strand":-1,"description":"ribosomal protein L12 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36619]"}, {"versioned_ensembl_gene_id":"ENSG00000204899.5","gene_symbol":"MZT1","gene_name":"mitotic spindle organizing protein 1 [Source:HGNC Symbol;Acc:HGNC:33830]","synonyms":"LOC440145,FLJ21869,C13orf37,RP11-11C5.2,MOZART1,MGC150539","biotype":"protein_coding","ncbi_id":"440145","summary":null,"start":72708357,"end":72727687,"strand":-1,"description":"mitotic spindle organizing protein 1 [Source:HGNC Symbol;Acc:HGNC:33830]"}, {"versioned_ensembl_gene_id":"ENSG00000115604.10","gene_symbol":"IL18R1","gene_name":"interleukin 18 receptor 1 [Source:HGNC Symbol;Acc:HGNC:5988]","synonyms":"IL1RRP,IL-1Rrp,CD218a","biotype":"protein_coding","ncbi_id":"8809","summary":"The protein encoded by this gene is a cytokine receptor that belongs to the interleukin 1 receptor family. This receptor specifically binds interleukin 18 (IL18), and is essential for IL18 mediated signal transduction. IFN-alpha and IL12 are reported to induce the expression of this receptor in NK and T cells. This gene along with four other members of the interleukin 1 receptor family, including IL1R2, IL1R1, ILRL2 (IL-1Rrp2), and IL1RL1 (T1/ST2), form a gene cluster on chromosome 2q. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":102311529,"end":102398775,"strand":1,"description":"interleukin 18 receptor 1 [Source:HGNC Symbol;Acc:HGNC:5988]"}, {"versioned_ensembl_gene_id":"ENSG00000249403.1","gene_symbol":"AC008413.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174986295,"end":174987050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255350.1","gene_symbol":"MTCO1P15","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075265","summary":null,"start":103404309,"end":103405834,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52017]"}, {"versioned_ensembl_gene_id":"ENSG00000266049.1","gene_symbol":"AP001011.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2688564,"end":2833065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169393.8","gene_symbol":"ELSPBP1","gene_name":"epididymal sperm binding protein 1 [Source:HGNC Symbol;Acc:HGNC:14417]","synonyms":"HE12,EDDM12,E12","biotype":"protein_coding","ncbi_id":"64100","summary":"The protein encoded by this gene belongs to the sperm-coating protein family of epididymal origin. This protein and its canine homolog are the first known examples of proteins with four tandemly arranged fibronectin type 2 (Fn2) domains in the Fn2-module protein family. [provided by RefSeq, Jul 2008]","start":47994651,"end":48025153,"strand":1,"description":"epididymal sperm binding protein 1 [Source:HGNC Symbol;Acc:HGNC:14417]"}, {"versioned_ensembl_gene_id":"ENSG00000118197.13","gene_symbol":"DDX59","gene_name":"DEAD-box helicase 59 [Source:HGNC Symbol;Acc:HGNC:25360]","synonyms":"ZNHIT5,DKFZP564B1023","biotype":"protein_coding","ncbi_id":"83479","summary":null,"start":200623896,"end":200669969,"strand":-1,"description":"DEAD-box helicase 59 [Source:HGNC Symbol;Acc:HGNC:25360]"}, {"versioned_ensembl_gene_id":"ENSG00000260088.1","gene_symbol":"AL445483.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":200669507,"end":200694250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282246.1","gene_symbol":"AL157392.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":13610047,"end":13655929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274211.4","gene_symbol":"SOCS7","gene_name":"suppressor of cytokine signaling 7 [Source:HGNC Symbol;Acc:HGNC:29846]","synonyms":"NCKAP4,NAP4","biotype":"protein_coding","ncbi_id":"30837","summary":null,"start":38352228,"end":38405593,"strand":1,"description":"suppressor of cytokine signaling 7 [Source:HGNC Symbol;Acc:HGNC:29846]"}, {"versioned_ensembl_gene_id":"ENSG00000144591.18","gene_symbol":"GMPPA","gene_name":"GDP-mannose pyrophosphorylase A [Source:HGNC Symbol;Acc:HGNC:22923]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29926","summary":"This gene is thought to encode a GDP-mannose pyrophosphorylase. This enzyme catalyzes the reaction which converts mannose-1-phosphate and GTP to GDP-mannose which is involved in the production of N-linked oligosaccharides. [provided by RefSeq, Jul 2008]","start":219498867,"end":219506989,"strand":1,"description":"GDP-mannose pyrophosphorylase A [Source:HGNC Symbol;Acc:HGNC:22923]"}, {"versioned_ensembl_gene_id":"ENSG00000188334.3","gene_symbol":"BSPH1","gene_name":"binder of sperm protein homolog 1 [Source:HGNC Symbol;Acc:HGNC:33906]","synonyms":"ELSPBP2,BSP1","biotype":"protein_coding","ncbi_id":"100131137","summary":null,"start":47968046,"end":47992170,"strand":-1,"description":"binder of sperm protein homolog 1 [Source:HGNC Symbol;Acc:HGNC:33906]"}, {"versioned_ensembl_gene_id":"ENSG00000175115.11","gene_symbol":"PACS1","gene_name":"phosphofurin acidic cluster sorting protein 1 [Source:HGNC Symbol;Acc:HGNC:30032]","synonyms":"KIAA1175,FLJ10209","biotype":"protein_coding","ncbi_id":"55690","summary":"This gene encodes a protein with a putative role in the localization of trans-Golgi network (TGN) membrane proteins. Mouse and rat homologs have been identified and studies of the homologous rat protein indicate a role in directing TGN localization of furin by binding to the protease's phosphorylated cytosolic domain. In addition, the human protein plays a role in HIV-1 Nef-mediated downregulation of cell surface MHC-I molecules to the TGN, thereby enabling HIV-1 to escape immune surveillance. [provided by RefSeq, Jul 2008]","start":66070363,"end":66244747,"strand":1,"description":"phosphofurin acidic cluster sorting protein 1 [Source:HGNC Symbol;Acc:HGNC:30032]"}, {"versioned_ensembl_gene_id":"ENSG00000277998.1","gene_symbol":"AC107075.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":164573741,"end":164574054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068120.14","gene_symbol":"COASY","gene_name":"Coenzyme A synthase [Source:HGNC Symbol;Acc:HGNC:29932]","synonyms":"PPAT,NBP,DPCK,CoASY","biotype":"protein_coding","ncbi_id":"80347","summary":"Coenzyme A (CoA) functions as a carrier of acetyl and acyl groups in cells and thus plays an important role in numerous synthetic and degradative metabolic pathways in all organisms. In eukaryotes, CoA and its derivatives are also involved in membrane trafficking and signal transduction. This gene encodes the bifunctional protein coenzyme A synthase (CoAsy) which carries out the last two steps in the biosynthesis of CoA from pantothenic acid (vitamin B5). The phosphopantetheine adenylyltransferase domain of this bifunctional protein catalyzes the conversion of 4'-phosphopantetheine into dephospho-coenzyme A (dpCoA) while its dephospho-CoA kinase domain completes the final step by phosphorylating dpCoA to form CoA. Mutations in this gene are associated with neurodegeneration with brain iron accumulation (NBIA). Alternative splicing results in multiple isoforms. [provided by RefSeq, Apr 2014]","start":42561467,"end":42566277,"strand":1,"description":"Coenzyme A synthase [Source:HGNC Symbol;Acc:HGNC:29932]"}, {"versioned_ensembl_gene_id":"ENSG00000251527.1","gene_symbol":"AC097110.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65858761,"end":65860204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278468.3","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195746774,"end":195792809,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000102900.12","gene_symbol":"NUP93","gene_name":"nucleoporin 93 [Source:HGNC Symbol;Acc:HGNC:28958]","synonyms":"KIAA0095","biotype":"protein_coding","ncbi_id":"9688","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. This gene encodes a nucleoporin protein that localizes both to the basket of the pore and to the nuclear entry of the central gated channel of the pore. The encoded protein is a target of caspase cysteine proteases that play a central role in programmed cell death by apoptosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":56730105,"end":56850286,"strand":1,"description":"nucleoporin 93 [Source:HGNC Symbol;Acc:HGNC:28958]"}, {"versioned_ensembl_gene_id":"ENSG00000115598.9","gene_symbol":"IL1RL2","gene_name":"interleukin 1 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:5999]","synonyms":"IL1RRP2,IL1R-rp2","biotype":"protein_coding","ncbi_id":"8808","summary":"The protein encoded by this gene is a member of the interleukin 1 receptor family. An experiment with transient gene expression demonstrated that this receptor was incapable of binding to interleukin 1 alpha and interleukin 1 beta with high affinity. This gene and four other interleukin 1 receptor family genes, including interleukin 1 receptor, type I (IL1R1), interleukin 1 receptor, type II (IL1R2), interleukin 1 receptor-like 1 (IL1RL1), and interleukin 18 receptor 1 (IL18R1), form a cytokine receptor gene cluster in a region mapped to chromosome 2q12. [provided by RefSeq, Jul 2008]","start":102186973,"end":102240002,"strand":1,"description":"interleukin 1 receptor like 2 [Source:HGNC Symbol;Acc:HGNC:5999]"}, {"versioned_ensembl_gene_id":"ENSG00000278845.4","gene_symbol":"MRPL45","gene_name":"mitochondrial ribosomal protein L45 [Source:HGNC Symbol;Acc:HGNC:16651]","synonyms":"MGC11321","biotype":"protein_coding","ncbi_id":"84311","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Alternative splicing results in multiple transcript variants. Pseudogenes corresponding to this gene are found on chromosomes 2p and 17q. [provided by RefSeq, May 2013]","start":38297023,"end":38323218,"strand":1,"description":"mitochondrial ribosomal protein L45 [Source:HGNC Symbol;Acc:HGNC:16651]"}, {"versioned_ensembl_gene_id":"ENSG00000235708.8","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"HKE5,DFNB53,DFNA13","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33333046,"end":33362862,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000143575.14","gene_symbol":"HAX1","gene_name":"HCLS1 associated protein X-1 [Source:HGNC Symbol;Acc:HGNC:16915]","synonyms":"HS1BP1,HCLSBP1","biotype":"protein_coding","ncbi_id":"10456","summary":"The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":154272511,"end":154275875,"strand":1,"description":"HCLS1 associated protein X-1 [Source:HGNC Symbol;Acc:HGNC:16915]"}, {"versioned_ensembl_gene_id":"ENSG00000164616.15","gene_symbol":"FBXL21","gene_name":"F-box and leucine rich repeat protein 21 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13600]","synonyms":"FBXL3P,FBXL3B,FBL3B,Fbl21","biotype":"transcribed_unitary_pseudogene","ncbi_id":"26223","summary":"This locus represents a transcribed pseudogene that is related to genes encoding members of the F-box family of proteins. [provided by RefSeq, Nov 2017]","start":135930317,"end":135951591,"strand":1,"description":"F-box and leucine rich repeat protein 21 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:13600]"}, {"versioned_ensembl_gene_id":"ENSG00000228123.4","gene_symbol":"AL162726.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82431889,"end":82432905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230360.1","gene_symbol":"DDX10P2","gene_name":"DEAD-box helicase 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44961]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401533","summary":null,"start":82086155,"end":82088768,"strand":-1,"description":"DEAD-box helicase 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44961]"}, {"versioned_ensembl_gene_id":"ENSG00000101246.19","gene_symbol":"ARFRP1","gene_name":"ADP ribosylation factor related protein 1 [Source:HGNC Symbol;Acc:HGNC:662]","synonyms":"Arp1,ARP,ARL18","biotype":"protein_coding","ncbi_id":"10139","summary":"The protein encoded by this gene is a membrane-associated GTP-ase which localizes to the plasma membrane and is related to the ADP-ribosylation factor (ARF) and ARF-like (ARL) proteins. This gene plays a role in membrane trafficking between the trans-Golgi network and endosomes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, May 2012]","start":63698642,"end":63708025,"strand":-1,"description":"ADP ribosylation factor related protein 1 [Source:HGNC Symbol;Acc:HGNC:662]"}, {"versioned_ensembl_gene_id":"ENSG00000273901.1","gene_symbol":"AC012313.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58500505,"end":58501137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284652.1","gene_symbol":"BX323043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9421098,"end":9422862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118058.20","gene_symbol":"KMT2A","gene_name":"lysine methyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:7132]","synonyms":"TRX1,MLL1A,MLL,HTRX1,HRX,CXXC7,ALL-1","biotype":"protein_coding","ncbi_id":"4297","summary":"This gene encodes a transcriptional coactivator that plays an essential role in regulating gene expression during early development and hematopoiesis. The encoded protein contains multiple conserved functional domains. One of these domains, the SET domain, is responsible for its histone H3 lysine 4 (H3K4) methyltransferase activity which mediates chromatin modifications associated with epigenetic transcriptional activation. This protein is processed by the enzyme Taspase 1 into two fragments, MLL-C and MLL-N. These fragments reassociate and further assemble into different multiprotein complexes that regulate the transcription of specific target genes, including many of the HOX genes. Multiple chromosomal translocations involving this gene are the cause of certain acute lymphoid leukemias and acute myeloid leukemias. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]","start":118436490,"end":118526832,"strand":1,"description":"lysine methyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:7132]"}, {"versioned_ensembl_gene_id":"ENSG00000119431.9","gene_symbol":"HDHD3","gene_name":"haloacid dehalogenase like hydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28171]","synonyms":"MGC12904,C9orf158","biotype":"protein_coding","ncbi_id":"81932","summary":null,"start":113373419,"end":113376999,"strand":-1,"description":"haloacid dehalogenase like hydrolase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28171]"}, {"versioned_ensembl_gene_id":"ENSG00000266179.2","gene_symbol":"AC025627.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19600860,"end":19601345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258671.2","gene_symbol":"AL132639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39211781,"end":39212255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248187.1","gene_symbol":"AC078850.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128567972,"end":128570531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235181.1","gene_symbol":"AC245036.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54551970,"end":54552256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273077.1","gene_symbol":"AC110609.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128552590,"end":128553416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203721.6","gene_symbol":"LINC00862","gene_name":"long intergenic non-protein coding RNA 862 [Source:HGNC Symbol;Acc:HGNC:21901]","synonyms":"SMIM16,C1orf98","biotype":"lincRNA","ncbi_id":"554279","summary":null,"start":200253419,"end":200400705,"strand":-1,"description":"long intergenic non-protein coding RNA 862 [Source:HGNC Symbol;Acc:HGNC:21901]"}, {"versioned_ensembl_gene_id":"ENSG00000233934.2","gene_symbol":"RPL21P38","gene_name":"ribosomal protein L21 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131481","summary":null,"start":171587093,"end":171587259,"strand":1,"description":"ribosomal protein L21 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36349]"}, {"versioned_ensembl_gene_id":"ENSG00000230457.3","gene_symbol":"PA2G4P4","gene_name":"proliferation-associated 2G4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32217]","synonyms":"PA2G4L1","biotype":"processed_pseudogene","ncbi_id":"647033","summary":null,"start":156809551,"end":156810732,"strand":-1,"description":"proliferation-associated 2G4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32217]"}, {"versioned_ensembl_gene_id":"ENSG00000249471.7","gene_symbol":"ZNF324B","gene_name":"zinc finger protein 324B [Source:HGNC Symbol;Acc:HGNC:33107]","synonyms":"FLJ45850","biotype":"protein_coding","ncbi_id":"388569","summary":null,"start":58451604,"end":58457833,"strand":1,"description":"zinc finger protein 324B [Source:HGNC Symbol;Acc:HGNC:33107]"}, {"versioned_ensembl_gene_id":"ENSG00000234187.1","gene_symbol":"AIMP1P1","gene_name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16543]","synonyms":"SCYE1P,bA400P21.1","biotype":"processed_pseudogene","ncbi_id":"170547","summary":null,"start":14127400,"end":14128336,"strand":1,"description":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16543]"}, {"versioned_ensembl_gene_id":"ENSG00000253520.1","gene_symbol":"AC136628.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179527224,"end":179527513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139433.9","gene_symbol":"GLTP","gene_name":"glycolipid transfer protein [Source:HGNC Symbol;Acc:HGNC:24867]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51228","summary":"The protein encoded by this gene is similar to bovine and porcine proteins which accelerate transfer of certain glycosphingolipids and glyceroglycolipids between membranes. It is thought to be a cytoplasmic protein. [provided by RefSeq, Jul 2008]","start":109850943,"end":109880488,"strand":-1,"description":"glycolipid transfer protein [Source:HGNC Symbol;Acc:HGNC:24867]"}, {"versioned_ensembl_gene_id":"ENSG00000271483.1","gene_symbol":"AC108676.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":194471923,"end":194472085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244675.2","gene_symbol":"AC108676.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":194496317,"end":194501503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280269.1","gene_symbol":"AP000577.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74204869,"end":74205746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253163.1","gene_symbol":"AC109479.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179377531,"end":179378761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203565.2","gene_symbol":"AL450313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33684755,"end":33687064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165996.13","gene_symbol":"HACD1","gene_name":"3-hydroxyacyl-CoA dehydratase 1 [Source:HGNC Symbol;Acc:HGNC:9639]","synonyms":"PTPLA,CAP","biotype":"protein_coding","ncbi_id":"9200","summary":"The protein encoded by this gene contains a characteristic catalytic motif of the protein tyrosine phosphatases (PTPs) family. The PTP motif of this protein has the highly conserved arginine residue replaced by a proline residue; thus it may represent a distinct class of PTPs. Members of the PTP family are known to be signaling molecules that regulate a variety of cellular processes. This gene was preferentially expressed in both adult and fetal heart. A much lower expression level was detected in skeletal and smooth muscle tissues, and no expression was observed in other tissues. The tissue specific expression in the developing and adult heart suggests a role in regulating cardiac development and differentiation. [provided by RefSeq, Jul 2008]","start":17589032,"end":17617377,"strand":-1,"description":"3-hydroxyacyl-CoA dehydratase 1 [Source:HGNC Symbol;Acc:HGNC:9639]"}, {"versioned_ensembl_gene_id":"ENSG00000253176.3","gene_symbol":"AC104997.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27838477,"end":27840382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121797.9","gene_symbol":"CCRL2","gene_name":"C-C motif chemokine receptor like 2 [Source:HGNC Symbol;Acc:HGNC:1612]","synonyms":"CRAM-A,CKRX,ACKR5,HCR,CRAM-B","biotype":"protein_coding","ncbi_id":"9034","summary":"This gene encodes a chemokine receptor like protein, which is predicted to be a seven transmembrane protein and most closely related to CCR1. Chemokines and their receptors mediated signal transduction are critical for the recruitment of effector immune cells to the site of inflammation. This gene is expressed at high levels in primary neutrophils and primary monocytes, and is further upregulated on neutrophil activation and during monocyte to macrophage differentiation. The function of this gene is unknown. This gene is mapped to the region where the chemokine receptor gene cluster is located. [provided by RefSeq, Jul 2008]","start":46407163,"end":46412997,"strand":1,"description":"C-C motif chemokine receptor like 2 [Source:HGNC Symbol;Acc:HGNC:1612]"}, {"versioned_ensembl_gene_id":"ENSG00000071967.11","gene_symbol":"CYBRD1","gene_name":"cytochrome b reductase 1 [Source:HGNC Symbol;Acc:HGNC:20797]","synonyms":"DCYTB,CYB561A2,FRRS3,FLJ23462","biotype":"protein_coding","ncbi_id":"79901","summary":"This gene is a member of the cytochrome b(561) family that encodes an iron-regulated protein. It highly expressed in the duodenal brush border membrane. It has ferric reductase activity and is believed to play a physiological role in dietary iron absorption. [provided by RefSeq, Jul 2008]","start":171522247,"end":171558133,"strand":1,"description":"cytochrome b reductase 1 [Source:HGNC Symbol;Acc:HGNC:20797]"}, {"versioned_ensembl_gene_id":"ENSG00000271585.1","gene_symbol":"AC011416.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127176696,"end":127177050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230182.1","gene_symbol":"RNF10P1","gene_name":"ring finger protein 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44472]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419599","summary":null,"start":5068676,"end":5069044,"strand":-1,"description":"ring finger protein 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44472]"}, {"versioned_ensembl_gene_id":"ENSG00000243509.4","gene_symbol":"TNFRSF6B","gene_name":"TNF receptor superfamily member 6b [Source:HGNC Symbol;Acc:HGNC:11921]","synonyms":"TR6,M68,DcR3","biotype":"protein_coding","ncbi_id":"8771","summary":"This gene belongs to the tumor necrosis factor receptor superfamily. The encoded protein is postulated to play a regulatory role in suppressing FasL- and LIGHT-mediated cell death. It acts as a decoy receptor that competes with death receptors for ligand binding. Over-expression of this gene has been noted in gastrointestinal tract tumors. Read-through transcription into this gene from the neighboring upstream gene, which encodes regulator of telomere elongation helicase 1 (RTEL1), generates a non-coding transcript. [provided by RefSeq, Feb 2011]","start":63696668,"end":63698684,"strand":1,"description":"TNF receptor superfamily member 6b [Source:HGNC Symbol;Acc:HGNC:11921]"}, {"versioned_ensembl_gene_id":"ENSG00000259030.6","gene_symbol":"FPGT-TNNI3K","gene_name":"FPGT-TNNI3K readthrough [Source:HGNC Symbol;Acc:HGNC:42952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526835","summary":"This locus represents naturally occurring read-through transcription from the neighboring fucose-1-phosphate guanylyltransferase (FPGT) and TNNI3 interacting kinase (TNNI3K) genes. Alternative splicing results in multiple transcript variants that are composed of in-frame exons from each individual gene. [provided by RefSeq, Dec 2010]","start":74198235,"end":74543982,"strand":1,"description":"FPGT-TNNI3K readthrough [Source:HGNC Symbol;Acc:HGNC:42952]"}, {"versioned_ensembl_gene_id":"ENSG00000229747.1","gene_symbol":"AL445687.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199908921,"end":199909648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274813.1","gene_symbol":"AC126915.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":178825382,"end":178825571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229299.2","gene_symbol":"AL121845.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63744689,"end":63745958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226580.1","gene_symbol":"RPL39P40","gene_name":"ribosomal protein L39 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:35823]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271531","summary":null,"start":17500679,"end":17500824,"strand":-1,"description":"ribosomal protein L39 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:35823]"}, {"versioned_ensembl_gene_id":"ENSG00000163888.3","gene_symbol":"CAMK2N2","gene_name":"calcium/calmodulin dependent protein kinase II inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:24197]","synonyms":"CaM-KIIN","biotype":"protein_coding","ncbi_id":"94032","summary":"This gene encodes a protein that is highly similar to the rat CaM-KII inhibitory protein, an inhibitor of calcium/calmodulin-dependent protein kinase II (CAMKII). CAMKII regulates numerous physiological functions, including neuronal synaptic plasticity through the phosphorylation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-type glutamate (AMPA) receptors. Studies of the similar protein in rat suggest that this protein may function as a negative regulator of CaM-KII and may act to inhibit the phosphorylation of AMPA receptors. [provided by RefSeq, Jul 2008]","start":184259213,"end":184261463,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:24197]"}, {"versioned_ensembl_gene_id":"ENSG00000231836.1","gene_symbol":"LINC01149","gene_name":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]","synonyms":"XXbac-BPG181B23.4","biotype":"processed_transcript","ncbi_id":"101929111","summary":null,"start":31484113,"end":31489410,"strand":1,"description":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]"}, {"versioned_ensembl_gene_id":"ENSG00000106536.19","gene_symbol":"POU6F2","gene_name":"POU class 6 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21694]","synonyms":"RPF-1","biotype":"protein_coding","ncbi_id":"11281","summary":"This gene encodes a member of the POU protein family characterized by the presence of a bipartite DNA binding domain, consisting of a POU-specific domain and a homeodomain, separated by a variable polylinker. The DNA binding domain may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner. The POU family members are transcriptional regulators, many of which are known to control cell type-specific differentiation pathways. This gene is a tumor suppressor involved in Wilms tumor (WT) predisposition. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":38977998,"end":39493095,"strand":1,"description":"POU class 6 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21694]"}, {"versioned_ensembl_gene_id":"ENSG00000182487.12","gene_symbol":"NCF1B","gene_name":"neutrophil cytosolic factor 1B pseudogene [Source:HGNC Symbol;Acc:HGNC:32522]","synonyms":"SH3PXD1B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"654816","summary":null,"start":73220624,"end":73235945,"strand":1,"description":"neutrophil cytosolic factor 1B pseudogene [Source:HGNC Symbol;Acc:HGNC:32522]"}, {"versioned_ensembl_gene_id":"ENSG00000116815.15","gene_symbol":"CD58","gene_name":"CD58 molecule [Source:HGNC Symbol;Acc:HGNC:1688]","synonyms":"LFA3","biotype":"protein_coding","ncbi_id":"965","summary":"This gene encodes a member of the immunoglobulin superfamily. The encoded protein is a ligand of the T lymphocyte CD2 protein, and functions in adhesion and activation of T lymphocytes. The protein is localized to the plasma membrane. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009]","start":116514535,"end":116571039,"strand":-1,"description":"CD58 molecule [Source:HGNC Symbol;Acc:HGNC:1688]"}, {"versioned_ensembl_gene_id":"ENSG00000224950.2","gene_symbol":"AL390066.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116493016,"end":116499212,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168309.16","gene_symbol":"FAM107A","gene_name":"family with sequence similarity 107 member A [Source:HGNC Symbol;Acc:HGNC:30827]","synonyms":"TU3A,DRR1","biotype":"protein_coding","ncbi_id":"11170","summary":null,"start":58564117,"end":58627610,"strand":-1,"description":"family with sequence similarity 107 member A [Source:HGNC Symbol;Acc:HGNC:30827]"}, {"versioned_ensembl_gene_id":"ENSG00000260256.1","gene_symbol":"AP001063.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44347767,"end":44348295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118503.14","gene_symbol":"TNFAIP3","gene_name":"TNF alpha induced protein 3 [Source:HGNC Symbol;Acc:HGNC:11896]","synonyms":"OTUD7C,A20","biotype":"protein_coding","ncbi_id":"7128","summary":"This gene was identified as a gene whose expression is rapidly induced by the tumor necrosis factor (TNF). The protein encoded by this gene is a zinc finger protein and ubiqitin-editing enzyme, and has been shown to inhibit NF-kappa B activation as well as TNF-mediated apoptosis. The encoded protein, which has both ubiquitin ligase and deubiquitinase activities, is involved in the cytokine-mediated immune and inflammatory responses. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2012]","start":137867188,"end":137883312,"strand":1,"description":"TNF alpha induced protein 3 [Source:HGNC Symbol;Acc:HGNC:11896]"}, {"versioned_ensembl_gene_id":"ENSG00000223479.3","gene_symbol":"LINC02238","gene_name":"long intergenic non-protein coding RNA 2238 [Source:HGNC Symbol;Acc:HGNC:53116]","synonyms":"RP4-788P17.1","biotype":"lincRNA","ncbi_id":"109729166","summary":null,"start":73635216,"end":73715214,"strand":1,"description":"long intergenic non-protein coding RNA 2238 [Source:HGNC Symbol;Acc:HGNC:53116]"}, {"versioned_ensembl_gene_id":"ENSG00000232716.2","gene_symbol":"AC016831.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130840204,"end":130843725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270761.1","gene_symbol":"AL355353.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47477243,"end":47477572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267289.1","gene_symbol":"AC008752.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9834079,"end":9835013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154380.17","gene_symbol":"ENAH","gene_name":"ENAH, actin regulator [Source:HGNC Symbol;Acc:HGNC:18271]","synonyms":"FLJ10773,NDPP1,MENA","biotype":"protein_coding","ncbi_id":"55740","summary":"This gene encodes a member of the enabled/ vasodilator-stimulated phosphoprotein. Members of this gene family are involved in actin-based motility. This protein is involved in regulating the assembly of actin filaments and modulates cell adhesion and motility. Alternate splice variants of this gene have been correlated with tumor invasiveness in certain tissues and these variants may serve as prognostic markers. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Sep 2016]","start":225486835,"end":225653142,"strand":-1,"description":"ENAH, actin regulator [Source:HGNC Symbol;Acc:HGNC:18271]"}, {"versioned_ensembl_gene_id":"ENSG00000100156.10","gene_symbol":"SLC16A8","gene_name":"solute carrier family 16 member 8 [Source:HGNC Symbol;Acc:HGNC:16270]","synonyms":"REMP,MCT3","biotype":"protein_coding","ncbi_id":"23539","summary":"SLC16A8 is a member of a family of proton-coupled monocarboxylate transporters that mediate lactate transport across cell membranes (Yoon et al., 1999 [PubMed 10493836]).[supplied by OMIM, Apr 2010]","start":38078134,"end":38084093,"strand":-1,"description":"solute carrier family 16 member 8 [Source:HGNC Symbol;Acc:HGNC:16270]"}, {"versioned_ensembl_gene_id":"ENSG00000153093.18","gene_symbol":"ACOXL","gene_name":"acyl-CoA oxidase like [Source:HGNC Symbol;Acc:HGNC:25621]","synonyms":"FLJ11042","biotype":"protein_coding","ncbi_id":"55289","summary":null,"start":110732573,"end":111118222,"strand":1,"description":"acyl-CoA oxidase like [Source:HGNC Symbol;Acc:HGNC:25621]"}, {"versioned_ensembl_gene_id":"ENSG00000140488.15","gene_symbol":"CELF6","gene_name":"CUGBP Elav-like family member 6 [Source:HGNC Symbol;Acc:HGNC:14059]","synonyms":"BRUNOL6","biotype":"protein_coding","ncbi_id":"60677","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]","start":72284727,"end":72320129,"strand":-1,"description":"CUGBP Elav-like family member 6 [Source:HGNC Symbol;Acc:HGNC:14059]"}, {"versioned_ensembl_gene_id":"ENSG00000176183.8","gene_symbol":"AC233964.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98338744,"end":98339832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248391.5","gene_symbol":"LINC02064","gene_name":"long intergenic non-protein coding RNA 2064 [Source:HGNC Symbol;Acc:HGNC:52909]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929681","summary":null,"start":29380296,"end":29395981,"strand":-1,"description":"long intergenic non-protein coding RNA 2064 [Source:HGNC Symbol;Acc:HGNC:52909]"}, {"versioned_ensembl_gene_id":"ENSG00000146072.6","gene_symbol":"TNFRSF21","gene_name":"TNF receptor superfamily member 21 [Source:HGNC Symbol;Acc:HGNC:13469]","synonyms":"DR6,CD358","biotype":"protein_coding","ncbi_id":"27242","summary":"This gene encodes a member of the tumor necrosis factor receptor superfamily. The encoded protein activates nuclear factor kappa-B and mitogen-activated protein kinase 8 (also called c-Jun N-terminal kinase 1), and induces cell apoptosis. Through its death domain, the encoded receptor interacts with tumor necrosis factor receptor type 1-associated death domain (TRADD) protein, which is known to mediate signal transduction of tumor necrosis factor receptors. Knockout studies in mice suggest that this gene plays a role in T-helper cell activation, and may be involved in inflammation and immune regulation. [provided by RefSeq, Jul 2013]","start":47231532,"end":47309905,"strand":-1,"description":"TNF receptor superfamily member 21 [Source:HGNC Symbol;Acc:HGNC:13469]"}, {"versioned_ensembl_gene_id":"ENSG00000276098.1","gene_symbol":"AC027345.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29516005,"end":29516504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248418.2","gene_symbol":"UBL5P1","gene_name":"ubiquitin like 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44639]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130803","summary":null,"start":29600676,"end":29600868,"strand":1,"description":"ubiquitin like 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44639]"}, {"versioned_ensembl_gene_id":"ENSG00000234181.1","gene_symbol":"AL353795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35096378,"end":35098141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130600.17","gene_symbol":"H19","gene_name":"H19, imprinted maternally expressed transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:4713]","synonyms":"NCRNA00008,LINC00008,D11S813E,ASM1,ASM","biotype":"processed_transcript","ncbi_id":"283120","summary":"This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":1995163,"end":2001470,"strand":-1,"description":"H19, imprinted maternally expressed transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:4713]"}, {"versioned_ensembl_gene_id":"ENSG00000167863.11","gene_symbol":"ATP5H","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D [Source:HGNC Symbol;Acc:HGNC:845]","synonyms":"ATPQ,ATP5JD","biotype":"protein_coding","ncbi_id":"10476","summary":"Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010]","start":75038863,"end":75046985,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D [Source:HGNC Symbol;Acc:HGNC:845]"}, {"versioned_ensembl_gene_id":"ENSG00000232788.1","gene_symbol":"AC078883.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172464262,"end":172466022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197651.4","gene_symbol":"CCER1","gene_name":"coiled-coil glutamate rich protein 1 [Source:HGNC Symbol;Acc:HGNC:28373]","synonyms":"MGC26598,C12orf12","biotype":"protein_coding","ncbi_id":"196477","summary":null,"start":90905622,"end":90955176,"strand":-1,"description":"coiled-coil glutamate rich protein 1 [Source:HGNC Symbol;Acc:HGNC:28373]"}, {"versioned_ensembl_gene_id":"ENSG00000180901.10","gene_symbol":"KCTD2","gene_name":"potassium channel tetramerization domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21294]","synonyms":"KIAA0176","biotype":"protein_coding","ncbi_id":"23510","summary":null,"start":75032575,"end":75065889,"strand":1,"description":"potassium channel tetramerization domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21294]"}, {"versioned_ensembl_gene_id":"ENSG00000109089.7","gene_symbol":"CDR2L","gene_name":"cerebellar degeneration related protein 2 like [Source:HGNC Symbol;Acc:HGNC:29999]","synonyms":"HUMPPA","biotype":"protein_coding","ncbi_id":"30850","summary":null,"start":74987632,"end":75005800,"strand":1,"description":"cerebellar degeneration related protein 2 like [Source:HGNC Symbol;Acc:HGNC:29999]"}, {"versioned_ensembl_gene_id":"ENSG00000276362.1","gene_symbol":"AC010087.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84850711,"end":84851148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232486.1","gene_symbol":"AL592437.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105758164,"end":105760755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282516.1","gene_symbol":"AC138747.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28422060,"end":28422264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101084.17","gene_symbol":"C20orf24","gene_name":"chromosome 20 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:15870]","synonyms":"RIP5,PNAS-11","biotype":"protein_coding","ncbi_id":"55969","summary":null,"start":36605734,"end":36612557,"strand":1,"description":"chromosome 20 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:15870]"}, {"versioned_ensembl_gene_id":"ENSG00000162676.11","gene_symbol":"GFI1","gene_name":"growth factor independent 1 transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:4237]","synonyms":"GFI-1,ZNF163,GFI1A","biotype":"protein_coding","ncbi_id":"2672","summary":"This gene encodes a nuclear zinc finger protein that functions as a transcriptional repressor. This protein plays a role in diverse developmental contexts, including hematopoiesis and oncogenesis. It functions as part of a complex along with other cofactors to control histone modifications that lead to silencing of the target gene promoters. Mutations in this gene cause autosomal dominant severe congenital neutropenia, and also dominant nonimmune chronic idiopathic neutropenia of adults, which are heterogeneous hematopoietic disorders that cause predispositions to leukemias and infections. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":92474762,"end":92486876,"strand":-1,"description":"growth factor independent 1 transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:4237]"}, {"versioned_ensembl_gene_id":"ENSG00000218536.1","gene_symbol":"AP002530.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102078872,"end":102079555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267530.2","gene_symbol":"LINC01836","gene_name":"long intergenic non-protein coding RNA 1836 [Source:HGNC Symbol;Acc:HGNC:52652]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985343","summary":null,"start":782755,"end":785080,"strand":1,"description":"long intergenic non-protein coding RNA 1836 [Source:HGNC Symbol;Acc:HGNC:52652]"}, {"versioned_ensembl_gene_id":"ENSG00000257194.2","gene_symbol":"AC126178.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90107739,"end":90112779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258290.1","gene_symbol":"BRWD1P2","gene_name":"bromodomain and WD repeat domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51529]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287505","summary":null,"start":89919437,"end":89919776,"strand":-1,"description":"bromodomain and WD repeat domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51529]"}, {"versioned_ensembl_gene_id":"ENSG00000259363.5","gene_symbol":"AC090825.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99807023,"end":99877148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276143.1","gene_symbol":"AC138747.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28402766,"end":28404923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259862.1","gene_symbol":"AC026336.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130249679,"end":130266725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242963.1","gene_symbol":"AC026336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130216807,"end":130217157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280144.1","gene_symbol":"AC073308.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":146050062,"end":146050366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166012.16","gene_symbol":"TAF1D","gene_name":"TATA-box binding protein associated factor, RNA polymerase I subunit D [Source:HGNC Symbol;Acc:HGNC:28759]","synonyms":"TAF(I)41,MGC5306,JOSD3","biotype":"protein_coding","ncbi_id":"79101","summary":"TAF1D is a member of the SL1 complex, which includes TBP (MIM 600075) and TAF1A (MIM 604903), TAF1B (MIM 604904), and TAF1C (MIM 604905), and plays a role in RNA polymerase I transcription (Wang et al., 2004 [PubMed 15520167]; Gorski et al., 2007 [PubMed 17318177]).[supplied by OMIM, Jun 2009]","start":93729948,"end":93784391,"strand":-1,"description":"TATA-box binding protein associated factor, RNA polymerase I subunit D [Source:HGNC Symbol;Acc:HGNC:28759]"}, {"versioned_ensembl_gene_id":"ENSG00000118903.6","gene_symbol":"BTF3P11","gene_name":"basic transcription factor 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:1126]","synonyms":"TNFRSF11B,OPG,OCIF,HUMBTFB,BTF3L1","biotype":"processed_pseudogene","ncbi_id":"690","summary":null,"start":76928066,"end":76928836,"strand":1,"description":"basic transcription factor 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:1126]"}, {"versioned_ensembl_gene_id":"ENSG00000178695.5","gene_symbol":"KCTD12","gene_name":"potassium channel tetramerization domain containing 12 [Source:HGNC Symbol;Acc:HGNC:14678]","synonyms":"PFET1,KIAA1778,C13orf2","biotype":"protein_coding","ncbi_id":"115207","summary":null,"start":76880166,"end":76886390,"strand":-1,"description":"potassium channel tetramerization domain containing 12 [Source:HGNC Symbol;Acc:HGNC:14678]"}, {"versioned_ensembl_gene_id":"ENSG00000238254.3","gene_symbol":"AC008496.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79849552,"end":79849846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270240.2","gene_symbol":"AC015849.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35868967,"end":35885863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250098.1","gene_symbol":"AC007370.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12947574,"end":12948670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142039.3","gene_symbol":"CCDC97","gene_name":"coiled-coil domain containing 97 [Source:HGNC Symbol;Acc:HGNC:28289]","synonyms":"MGC20255,FLJ40267","biotype":"protein_coding","ncbi_id":"90324","summary":null,"start":41310189,"end":41324883,"strand":1,"description":"coiled-coil domain containing 97 [Source:HGNC Symbol;Acc:HGNC:28289]"}, {"versioned_ensembl_gene_id":"ENSG00000198492.15","gene_symbol":"YTHDF2","gene_name":"YTH N6-methyladenosine RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:31675]","synonyms":"CAHL,NY-REN-2,HGRG8","biotype":"protein_coding","ncbi_id":"51441","summary":"This gene encodes a member of the YTH (YT521-B homology) superfamily containing YTH domain. The YTH domain is typical for the eukaryotes and is particularly abundant in plants. The YTH domain is usually located in the middle of the protein sequence and may function in binding to RNA. In addition to a YTH domain, this protein has a proline rich region which may be involved in signal transduction. An Alu-rich domain has been identified in one of the introns of this gene, which is thought to be associated with human longevity. In addition, reciprocal translocations between this gene and the Runx1 (AML1) gene on chromosome 21 has been observed in patients with acute myeloid leukemia. This gene was initially mapped to chromosome 14, which was later turned out to be a pseudogene. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Oct 2012]","start":28736621,"end":28769775,"strand":1,"description":"YTH N6-methyladenosine RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:31675]"}, {"versioned_ensembl_gene_id":"ENSG00000270936.1","gene_symbol":"AL034351.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210462345,"end":210463012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279193.1","gene_symbol":"AC026336.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130121925,"end":130122974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123810.7","gene_symbol":"B9D2","gene_name":"B9 protein domain 2 [Source:HGNC Symbol;Acc:HGNC:28636]","synonyms":"MKS10,MGC4093","biotype":"protein_coding","ncbi_id":"80776","summary":"This gene encodes a B9 domain protein, which are exclusively found in ciliated organisms. The gene is upregulated during mucociliary differentiation, and the encoded protein localizes to basal bodies and cilia. Disrupting expression of this gene results in ciliogenesis defects. [provided by RefSeq, Oct 2009]","start":41354421,"end":41364173,"strand":-1,"description":"B9 protein domain 2 [Source:HGNC Symbol;Acc:HGNC:28636]"}, {"versioned_ensembl_gene_id":"ENSG00000232144.1","gene_symbol":"PSAT1P2","gene_name":"phosphoserine aminotransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43988]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107133519","summary":null,"start":62552463,"end":62553434,"strand":-1,"description":"phosphoserine aminotransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43988]"}, {"versioned_ensembl_gene_id":"ENSG00000235845.1","gene_symbol":"AC098649.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44899178,"end":44900925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090989.17","gene_symbol":"EXOC1","gene_name":"exocyst complex component 1 [Source:HGNC Symbol;Acc:HGNC:30380]","synonyms":"Sec3p,SEC3L1,SEC3,FLJ10893,BM-102","biotype":"protein_coding","ncbi_id":"55763","summary":"The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":55853616,"end":55905034,"strand":1,"description":"exocyst complex component 1 [Source:HGNC Symbol;Acc:HGNC:30380]"}, {"versioned_ensembl_gene_id":"ENSG00000232618.1","gene_symbol":"AL355304.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142950211,"end":142956646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254976.1","gene_symbol":"AP001804.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":124324871,"end":124325789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169031.18","gene_symbol":"COL4A3","gene_name":"collagen type IV alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2204]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1285","summary":"Type IV collagen, the major structural component of basement membranes, is a multimeric protein composed of 3 alpha subunits. These subunits are encoded by 6 different genes, alpha 1 through alpha 6, each of which can form a triple helix structure with 2 other subunits to form type IV collagen. This gene encodes alpha 3. In the Goodpasture syndrome, autoantibodies bind to the collagen molecules in the basement membranes of alveoli and glomeruli. The epitopes that elicit these autoantibodies are localized largely to the non-collagenous C-terminal domain of the protein. A specific kinase phosphorylates amino acids in this same C-terminal region and the expression of this kinase is upregulated during pathogenesis. This gene is also linked to an autosomal recessive form of Alport syndrome. The mutations contributing to this syndrome are also located within the exons that encode this C-terminal region. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. [provided by RefSeq, Jun 2010]","start":227164565,"end":227314792,"strand":1,"description":"collagen type IV alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2204]"}, {"versioned_ensembl_gene_id":"ENSG00000261206.1","gene_symbol":"LINC00561","gene_name":"long intergenic non-protein coding RNA 561 [Source:HGNC Symbol;Acc:HGNC:43705]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861545","summary":null,"start":75932395,"end":75935132,"strand":-1,"description":"long intergenic non-protein coding RNA 561 [Source:HGNC Symbol;Acc:HGNC:43705]"}, {"versioned_ensembl_gene_id":"ENSG00000105329.9","gene_symbol":"TGFB1","gene_name":"transforming growth factor beta 1 [Source:HGNC Symbol;Acc:HGNC:11766]","synonyms":"TGFbeta,TGFB,DPD1,CED","biotype":"protein_coding","ncbi_id":"7040","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate a latency-associated peptide (LAP) and a mature peptide, and is found in either a latent form composed of a mature peptide homodimer, a LAP homodimer, and a latent TGF-beta binding protein, or in an active form consisting solely of the mature peptide homodimer. The mature peptide may also form heterodimers with other TGFB family members. This encoded protein regulates cell proliferation, differentiation and growth, and can modulate expression and activation of other growth factors including interferon gamma and tumor necrosis factor alpha. This gene is frequently upregulated in tumor cells, and mutations in this gene result in Camurati-Engelmann disease. [provided by RefSeq, Aug 2016]","start":41301587,"end":41353911,"strand":-1,"description":"transforming growth factor beta 1 [Source:HGNC Symbol;Acc:HGNC:11766]"}, {"versioned_ensembl_gene_id":"ENSG00000242520.5","gene_symbol":"MAGEA5","gene_name":"MAGE family member A5 [Source:HGNC Symbol;Acc:HGNC:6803]","synonyms":"MGC129526,MAGE5,CT1.5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4104","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This MAGEA gene is interpreted to be a pseudogene. Read-through transcription exists between this gene and the upstream melanoma antigen family A, 10 (MAGEA10) gene. [provided by RefSeq, Dec 2020]","start":152114599,"end":152115540,"strand":-1,"description":"MAGE family member A5 [Source:HGNC Symbol;Acc:HGNC:6803]"}, {"versioned_ensembl_gene_id":"ENSG00000255730.5","gene_symbol":"AC011462.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41350853,"end":41425001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137463.4","gene_symbol":"MGARP","gene_name":"mitochondria localized glutamic acid rich protein [Source:HGNC Symbol;Acc:HGNC:29969]","synonyms":"OSAP,HUMMR,CESP-1,C4orf49","biotype":"protein_coding","ncbi_id":"84709","summary":null,"start":139266163,"end":139280338,"strand":-1,"description":"mitochondria localized glutamic acid rich protein [Source:HGNC Symbol;Acc:HGNC:29969]"}, {"versioned_ensembl_gene_id":"ENSG00000261574.1","gene_symbol":"AC092120.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89392375,"end":89412564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091490.10","gene_symbol":"SEL1L3","gene_name":"SEL1L family member 3 [Source:HGNC Symbol;Acc:HGNC:29108]","synonyms":"KIAA0746","biotype":"protein_coding","ncbi_id":"23231","summary":null,"start":25747427,"end":25863760,"strand":-1,"description":"SEL1L family member 3 [Source:HGNC Symbol;Acc:HGNC:29108]"}, {"versioned_ensembl_gene_id":"ENSG00000260279.2","gene_symbol":"AC137932.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89297508,"end":89298317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103034.14","gene_symbol":"NDRG4","gene_name":"NDRG family member 4 [Source:HGNC Symbol;Acc:HGNC:14466]","synonyms":"SMAP-8,KIAA1180","biotype":"protein_coding","ncbi_id":"65009","summary":"This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein that is required for cell cycle progression and survival in primary astrocytes and may be involved in the regulation of mitogenic signalling in vascular smooth muscles cells. Alternative splicing results in multiple transcripts encoding different isoforms.[provided by RefSeq, Jun 2011]","start":58462846,"end":58513628,"strand":1,"description":"NDRG family member 4 [Source:HGNC Symbol;Acc:HGNC:14466]"}, {"versioned_ensembl_gene_id":"ENSG00000236052.1","gene_symbol":"LINC01643","gene_name":"long intergenic non-protein coding RNA 1643 [Source:HGNC Symbol;Acc:HGNC:52430]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373010","summary":null,"start":34017473,"end":34188425,"strand":1,"description":"long intergenic non-protein coding RNA 1643 [Source:HGNC Symbol;Acc:HGNC:52430]"}, {"versioned_ensembl_gene_id":"ENSG00000233014.1","gene_symbol":"TBC1D3P7","gene_name":"TBC1 domain family member 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43569]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480773","summary":null,"start":41323427,"end":41329545,"strand":1,"description":"TBC1 domain family member 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43569]"}, {"versioned_ensembl_gene_id":"ENSG00000198083.9","gene_symbol":"KRTAP9-9","gene_name":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]","synonyms":"KRTAP9-5,KAP9.9,KAP9.5,KRTAP9-5,KAP9.9,KAP9.5","biotype":"protein_coding","ncbi_id":"81870","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. Alternative haplotypes of this gene are represented in the GRCh38 reference genome assembly. [provided by RefSeq, Dec 2015]","start":41255384,"end":41256364,"strand":1,"description":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]"}, {"versioned_ensembl_gene_id":"ENSG00000229383.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529901,"end":29534049,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000257355.1","gene_symbol":"AC008770.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12017888,"end":12052967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196096.3","gene_symbol":"AC079610.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":213276552,"end":213284205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113525.9","gene_symbol":"IL5","gene_name":"interleukin 5 [Source:HGNC Symbol;Acc:HGNC:6016]","synonyms":"TRF,IL-5,EDF","biotype":"protein_coding","ncbi_id":"3567","summary":"This gene encodes a cytokine that acts as a growth and differentiation factor for both B cells and eosinophils. The encoded cytokine plays a major role in the regulation of eosinophil formation, maturation, recruitment and survival. The increased production of this cytokine may be related to pathogenesis of eosinophil-dependent inflammatory diseases. This cytokine functions by binding to its receptor, which is a heterodimer, whose beta subunit is shared with the receptors for interleukine 3 (IL3) and colony stimulating factor 2 (CSF2/GM-CSF). This gene is located on chromosome 5 within a cytokine gene cluster which includes interleukin 4 (IL4), interleukin 13 (IL13), and CSF2 . This gene, IL4, and IL13 may be regulated coordinately by long-range regulatory elements spread over 120 kilobases on chromosome 5q31. [provided by RefSeq, Jul 2013]","start":132541444,"end":132556838,"strand":-1,"description":"interleukin 5 [Source:HGNC Symbol;Acc:HGNC:6016]"}, {"versioned_ensembl_gene_id":"ENSG00000188316.13","gene_symbol":"ENO4","gene_name":"enolase family member 4 [Source:HGNC Symbol;Acc:HGNC:31670]","synonyms":"C10orf134,AC023283.3","biotype":"protein_coding","ncbi_id":"387712","summary":null,"start":116849512,"end":116911788,"strand":1,"description":"enolase family member 4 [Source:HGNC Symbol;Acc:HGNC:31670]"}, {"versioned_ensembl_gene_id":"ENSG00000173077.14","gene_symbol":"DEC1","gene_name":"deleted in esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:23658]","synonyms":"CTS9","biotype":"protein_coding","ncbi_id":"50514","summary":"The function of this gene is not known. This gene is located in a region commonly deleted in esophageal squamous cell carcinomas. Gene expression is reduced or absent in these carcinomas and thus this is a candidate tumor suppressor gene for esophageal squamous cell carcinomas. [provided by RefSeq, Jul 2008]","start":115141818,"end":115402644,"strand":1,"description":"deleted in esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:23658]"}, {"versioned_ensembl_gene_id":"ENSG00000275452.2","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"cl-49,nkat5,183ActI,CD158J","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738501,"end":54769226,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000250328.5","gene_symbol":"MGC32805","gene_name":"uncharacterized LOC153163 [Source:NCBI gene;Acc:153163]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"153163","summary":null,"start":122436497,"end":122479087,"strand":-1,"description":"uncharacterized LOC153163 [Source:NCBI gene;Acc:153163]"}, {"versioned_ensembl_gene_id":"ENSG00000197249.13","gene_symbol":"SERPINA1","gene_name":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]","synonyms":"AAT,A1AT,A1A,PI1,PI,alpha1AT,alpha-1-antitrypsin","biotype":"protein_coding","ncbi_id":"5265","summary":"The protein encoded by this gene is a serine protease inhibitor belonging to the serpin superfamily whose targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, and plasminogen activator. This protein is produced in the liver, the bone marrow, by lymphocytic and monocytic cells in lymphoid tissue, and by the Paneth cells of the gut. Defects in this gene are associated with chronic obstructive pulmonary disease, emphysema, and chronic liver disease. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2020]","start":94376747,"end":94390693,"strand":-1,"description":"serpin family A member 1 [Source:HGNC Symbol;Acc:HGNC:8941]"}, {"versioned_ensembl_gene_id":"ENSG00000170703.15","gene_symbol":"TTLL6","gene_name":"tubulin tyrosine ligase like 6 [Source:HGNC Symbol;Acc:HGNC:26664]","synonyms":"FLJ35808","biotype":"protein_coding","ncbi_id":"284076","summary":null,"start":48762235,"end":48817214,"strand":-1,"description":"tubulin tyrosine ligase like 6 [Source:HGNC Symbol;Acc:HGNC:26664]"}, {"versioned_ensembl_gene_id":"ENSG00000088325.15","gene_symbol":"TPX2","gene_name":"TPX2, microtubule nucleation factor [Source:HGNC Symbol;Acc:HGNC:1249]","synonyms":"C20orf1,p100,DIL-2,C20orf2","biotype":"protein_coding","ncbi_id":"22974","summary":null,"start":31739271,"end":31801805,"strand":1,"description":"TPX2, microtubule nucleation factor [Source:HGNC Symbol;Acc:HGNC:1249]"}, {"versioned_ensembl_gene_id":"ENSG00000276255.2","gene_symbol":"AL136379.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":228073909,"end":228076550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159182.4","gene_symbol":"PRAC1","gene_name":"PRAC1 small nuclear protein [Source:HGNC Symbol;Acc:HGNC:30591]","synonyms":"PRAC,C17orf92","biotype":"protein_coding","ncbi_id":"84366","summary":"This gene is reported to be specifically expressed in prostate, rectum and distal colon. Sequence analysis suggests that it may play a regulatory role in the nucleus. [provided by RefSeq, Jul 2008]","start":48721719,"end":48722522,"strand":-1,"description":"PRAC1 small nuclear protein [Source:HGNC Symbol;Acc:HGNC:30591]"}, {"versioned_ensembl_gene_id":"ENSG00000239741.3","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"NG32,C6orf21,LY6G6D,G6f","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31746341,"end":31750054,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000241788.2","gene_symbol":"COX6B1P2","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2282]","synonyms":"COX6BP2","biotype":"processed_pseudogene","ncbi_id":"1342","summary":null,"start":48713730,"end":48713959,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2282]"}, {"versioned_ensembl_gene_id":"ENSG00000271240.1","gene_symbol":"AC110741.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133962992,"end":133963259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253627.1","gene_symbol":"AC105180.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134211865,"end":134320447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253593.2","gene_symbol":"AC110741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133886496,"end":133902407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263345.1","gene_symbol":"AC006435.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2375061,"end":2379306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196933.5","gene_symbol":"RPS26P11","gene_name":"ribosomal protein S26 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:31817]","synonyms":"RPS26L1,bA366E13.1","biotype":"processed_pseudogene","ncbi_id":"441502","summary":null,"start":72044545,"end":72044892,"strand":1,"description":"ribosomal protein S26 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:31817]"}, {"versioned_ensembl_gene_id":"ENSG00000225084.1","gene_symbol":"AL450226.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2232680,"end":2233610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279040.1","gene_symbol":"AC090617.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2101542,"end":2101667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204131.9","gene_symbol":"NHSL2","gene_name":"NHS like 2 [Source:HGNC Symbol;Acc:HGNC:33737]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340527","summary":null,"start":71910818,"end":72161750,"strand":1,"description":"NHS like 2 [Source:HGNC Symbol;Acc:HGNC:33737]"}, {"versioned_ensembl_gene_id":"ENSG00000232630.1","gene_symbol":"PRPS1P2","gene_name":"phosphoribosyl pyrophosphate synthetase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9464]","synonyms":"PRPS1L2","biotype":"processed_pseudogene","ncbi_id":"100421295","summary":null,"start":125150653,"end":125151589,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9464]"}, {"versioned_ensembl_gene_id":"ENSG00000105220.14","gene_symbol":"GPI","gene_name":"glucose-6-phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:4458]","synonyms":"NLK,AMF","biotype":"protein_coding","ncbi_id":"2821","summary":"This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phosphate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":34359480,"end":34402156,"strand":1,"description":"glucose-6-phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:4458]"}, {"versioned_ensembl_gene_id":"ENSG00000279221.1","gene_symbol":"AC068254.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69659837,"end":69663413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265643.1","gene_symbol":"AC119868.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69483627,"end":69618694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257008.6","gene_symbol":"GPR142","gene_name":"G protein-coupled receptor 142 [Source:HGNC Symbol;Acc:HGNC:20088]","synonyms":"PGR2","biotype":"protein_coding","ncbi_id":"350383","summary":"GPR142 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003 [PubMed 14623098]).[supplied by OMIM, Mar 2008]","start":74367407,"end":74372622,"strand":1,"description":"G protein-coupled receptor 142 [Source:HGNC Symbol;Acc:HGNC:20088]"}, {"versioned_ensembl_gene_id":"ENSG00000204347.3","gene_symbol":"BTBD17","gene_name":"BTB domain containing 17 [Source:HGNC Symbol;Acc:HGNC:33758]","synonyms":"TANGO10A,LGALS3BPL,BTBD17A","biotype":"protein_coding","ncbi_id":"388419","summary":null,"start":74356416,"end":74361946,"strand":-1,"description":"BTB domain containing 17 [Source:HGNC Symbol;Acc:HGNC:33758]"}, {"versioned_ensembl_gene_id":"ENSG00000233964.2","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29920543,"end":29923320,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000236203.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29986556,"end":29987433,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000196757.7","gene_symbol":"ZNF700","gene_name":"zinc finger protein 700 [Source:HGNC Symbol;Acc:HGNC:25292]","synonyms":"DKFZp434I1610","biotype":"protein_coding","ncbi_id":"90592","summary":null,"start":11925068,"end":11950773,"strand":1,"description":"zinc finger protein 700 [Source:HGNC Symbol;Acc:HGNC:25292]"}, {"versioned_ensembl_gene_id":"ENSG00000263050.1","gene_symbol":"AC090617.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2043475,"end":2044968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170214.4","gene_symbol":"ADRA1B","gene_name":"adrenoceptor alpha 1B [Source:HGNC Symbol;Acc:HGNC:278]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147","summary":"Alpha-1-adrenergic receptors (alpha-1-ARs) are members of the G protein-coupled receptor superfamily. They activate mitogenic responses and regulate growth and proliferation of many cells. There are 3 alpha-1-AR subtypes: alpha-1A, -1B and -1D, all of which signal through the Gq/11 family of G-proteins and different subtypes show different patterns of activation. This gene encodes alpha-1B-adrenergic receptor, which induces neoplastic transformation when transfected into NIH 3T3 fibroblasts and other cell lines. Thus, this normal cellular gene is identified as a protooncogene. This gene comprises 2 exons and a single large intron of at least 20 kb that interrupts the coding region. [provided by RefSeq, Jul 2008]","start":159865080,"end":159972544,"strand":1,"description":"adrenoceptor alpha 1B [Source:HGNC Symbol;Acc:HGNC:278]"}, {"versioned_ensembl_gene_id":"ENSG00000150637.8","gene_symbol":"CD226","gene_name":"CD226 molecule [Source:HGNC Symbol;Acc:HGNC:16961]","synonyms":"TLiSA1,PTA1,DNAM1,DNAM-1","biotype":"protein_coding","ncbi_id":"10666","summary":"This gene encodes a glycoprotein expressed on the surface of NK cells, platelets, monocytes and a subset of T cells. It is a member of the Ig-superfamily containing 2 Ig-like domains of the V-set. The protein mediates cellular adhesion of platelets and megakaryocytic cells to vascular endothelial cells. The protein also plays a role in megakaryocytic cell maturation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":69831158,"end":69961803,"strand":-1,"description":"CD226 molecule [Source:HGNC Symbol;Acc:HGNC:16961]"}, {"versioned_ensembl_gene_id":"ENSG00000268015.1","gene_symbol":"AC010320.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52222225,"end":52231294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119632.3","gene_symbol":"IFI27L2","gene_name":"interferon alpha inducible protein 27 like 2 [Source:HGNC Symbol;Acc:HGNC:19753]","synonyms":"TLH29,FAM14A","biotype":"protein_coding","ncbi_id":"83982","summary":null,"start":94127779,"end":94130253,"strand":-1,"description":"interferon alpha inducible protein 27 like 2 [Source:HGNC Symbol;Acc:HGNC:19753]"}, {"versioned_ensembl_gene_id":"ENSG00000126653.17","gene_symbol":"NSRP1","gene_name":"nuclear speckle splicing regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:25305]","synonyms":"NSrp70,DKFZP434K1421,CCDC55","biotype":"protein_coding","ncbi_id":"84081","summary":null,"start":30115521,"end":30186475,"strand":1,"description":"nuclear speckle splicing regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:25305]"}, {"versioned_ensembl_gene_id":"ENSG00000054267.21","gene_symbol":"ARID4B","gene_name":"AT-rich interaction domain 4B [Source:HGNC Symbol;Acc:HGNC:15550]","synonyms":"SAP180,RBP1L1,BRCAA1,BCAA","biotype":"protein_coding","ncbi_id":"51742","summary":"This gene encodes a protein with sequence similarity to retinoblastoma-binding protein-1. The encoded protein is a subunit of the histone deacetylase-dependant SIN3A transcriptional corepressor complex, which functions in diverse cellular processes including proliferation, differentiation, apoptosis, oncogenesis, and cell fate determination. The gene product is recognized by IgG antibody isolated from a breast cancer patient and appears to be a molecular marker associated with a broad range of human malignancies. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008]","start":235131634,"end":235328219,"strand":-1,"description":"AT-rich interaction domain 4B [Source:HGNC Symbol;Acc:HGNC:15550]"}, {"versioned_ensembl_gene_id":"ENSG00000266876.1","gene_symbol":"AC104996.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":30068632,"end":30069631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225746.9","gene_symbol":"MEG8","gene_name":"maternally expressed 8, small nucleolar RNA host gene [Source:HGNC Symbol;Acc:HGNC:14574]","synonyms":"AL132709.8,SNHG24,SNHG23,Rian,NCRNA00024,lnc-MGC,LINC00024,Irm,Bsr","biotype":"lincRNA","ncbi_id":"79104","summary":"This gene is located in a cluster of imprinted genes on chromosome 14q32.3. It encodes a a non-protein coding transcript that is preferentially expressed from the maternal allele in skeletal muscle, and appears to be coordinately regulated with other imprinted genes in this region. [provided by RefSeq, Oct 2010]","start":100894770,"end":101027415,"strand":1,"description":"maternally expressed 8, small nucleolar RNA host gene [Source:HGNC Symbol;Acc:HGNC:14574]"}, {"versioned_ensembl_gene_id":"ENSG00000171595.13","gene_symbol":"DNAI2","gene_name":"dynein axonemal intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:18744]","synonyms":"DIC2,CILD9","biotype":"protein_coding","ncbi_id":"64446","summary":"The protein encoded by this gene belongs to the dynein intermediate chain family, and is part of the dynein complex of respiratory cilia and sperm flagella. Mutations in this gene are associated with primary ciliary dyskinesia type 9. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010]","start":74274247,"end":74314884,"strand":1,"description":"dynein axonemal intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:18744]"}, {"versioned_ensembl_gene_id":"ENSG00000266106.1","gene_symbol":"AC103809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74307210,"end":74309790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251204.1","gene_symbol":"AC027313.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106415576,"end":106417241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236863.2","gene_symbol":"RPL23AP23","gene_name":"ribosomal protein L23a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36272]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271292","summary":null,"start":235295865,"end":235296335,"strand":1,"description":"ribosomal protein L23a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36272]"}, {"versioned_ensembl_gene_id":"ENSG00000167363.13","gene_symbol":"FN3K","gene_name":"fructosamine 3 kinase [Source:HGNC Symbol;Acc:HGNC:24822]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64122","summary":"A high concentration of glucose can result in non-enzymatic oxidation of proteins by reaction of glucose and lysine residues (glycation). Proteins modified in this way, fructosamines, are less active or functional. This gene encodes an enzyme which catalyzes the phosphorylation of fructosamines which may result in deglycation. [provided by RefSeq, Feb 2012]","start":82735575,"end":82751197,"strand":1,"description":"fructosamine 3 kinase [Source:HGNC Symbol;Acc:HGNC:24822]"}, {"versioned_ensembl_gene_id":"ENSG00000244662.1","gene_symbol":"AC087312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24642687,"end":24643166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256674.1","gene_symbol":"AC020549.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114583253,"end":114584692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228509.5","gene_symbol":"AC006460.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190676944,"end":190708716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241458.1","gene_symbol":"RPL7P19","gene_name":"ribosomal protein L7 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36268]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270853","summary":null,"start":138473744,"end":138474361,"strand":1,"description":"ribosomal protein L7 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36268]"}, {"versioned_ensembl_gene_id":"ENSG00000279613.1","gene_symbol":"AC124283.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82648849,"end":82650657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248944.1","gene_symbol":"FAM90A6P","gene_name":"family with sequence similarity 90 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32254]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"389618","summary":null,"start":7549053,"end":7552062,"strand":-1,"description":"family with sequence similarity 90 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32254]"}, {"versioned_ensembl_gene_id":"ENSG00000185915.5","gene_symbol":"KLHL34","gene_name":"kelch like family member 34 [Source:HGNC Symbol;Acc:HGNC:26634]","synonyms":"RP11-450P7.3,FLJ34960","biotype":"protein_coding","ncbi_id":"257240","summary":null,"start":21654690,"end":21658330,"strand":-1,"description":"kelch like family member 34 [Source:HGNC Symbol;Acc:HGNC:26634]"}, {"versioned_ensembl_gene_id":"ENSG00000230626.4","gene_symbol":"AC011005.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":129126518,"end":129130793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234831.1","gene_symbol":"CR759913.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29934229,"end":29935221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145860.11","gene_symbol":"RNF145","gene_name":"ring finger protein 145 [Source:HGNC Symbol;Acc:HGNC:20853]","synonyms":"FLJ31951","biotype":"protein_coding","ncbi_id":"153830","summary":null,"start":159157409,"end":159210053,"strand":-1,"description":"ring finger protein 145 [Source:HGNC Symbol;Acc:HGNC:20853]"}, {"versioned_ensembl_gene_id":"ENSG00000235144.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29948716,"end":29950690,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000253756.1","gene_symbol":"CARSP2","gene_name":"cysteinyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50478]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481707","summary":null,"start":114791653,"end":114791929,"strand":-1,"description":"cysteinyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50478]"}, {"versioned_ensembl_gene_id":"ENSG00000168827.14","gene_symbol":"GFM1","gene_name":"G elongation factor mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:13780]","synonyms":"GFM,EGF1,EFGM","biotype":"protein_coding","ncbi_id":"85476","summary":"Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known. [provided by RefSeq, Jul 2008]","start":158644278,"end":158692575,"strand":1,"description":"G elongation factor mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:13780]"}, {"versioned_ensembl_gene_id":"ENSG00000227725.3","gene_symbol":"GCOM2","gene_name":"GRINL1B complex locus 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15712]","synonyms":"GRINL1B,GLURR2","biotype":"processed_pseudogene","ncbi_id":"339970","summary":null,"start":68038544,"end":68039647,"strand":1,"description":"GRINL1B complex locus 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15712]"}, {"versioned_ensembl_gene_id":"ENSG00000250905.1","gene_symbol":"AC093893.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149666057,"end":149711149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266522.1","gene_symbol":"AP005242.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15003975,"end":15006352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197023.6","gene_symbol":"OR51A6P","gene_name":"olfactory receptor family 51 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15187]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390046","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4889593,"end":4890596,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15187]"}, {"versioned_ensembl_gene_id":"ENSG00000231913.1","gene_symbol":"RARRES2P3","gene_name":"retinoic acid receptor responder 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48702]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481659","summary":null,"start":21421822,"end":21422294,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48702]"}, {"versioned_ensembl_gene_id":"ENSG00000126231.13","gene_symbol":"PROZ","gene_name":"protein Z, vitamin K dependent plasma glycoprotein [Source:HGNC Symbol;Acc:HGNC:9460]","synonyms":"PZ","biotype":"protein_coding","ncbi_id":"8858","summary":"This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":113158654,"end":113172383,"strand":1,"description":"protein Z, vitamin K dependent plasma glycoprotein [Source:HGNC Symbol;Acc:HGNC:9460]"}, {"versioned_ensembl_gene_id":"ENSG00000242162.1","gene_symbol":"AC018639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129066021,"end":129066462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233347.1","gene_symbol":"ERP29P1","gene_name":"endoplasmic reticulum lumenal protein 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24625]","synonyms":"ERP28P","biotype":"processed_pseudogene","ncbi_id":"100420612","summary":null,"start":52110344,"end":52111049,"strand":-1,"description":"endoplasmic reticulum lumenal protein 29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24625]"}, {"versioned_ensembl_gene_id":"ENSG00000237751.2","gene_symbol":"LINC01143","gene_name":"long intergenic non-protein coding RNA 1143 [Source:HGNC Symbol;Acc:HGNC:49458]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355141","summary":null,"start":70887871,"end":70889959,"strand":1,"description":"long intergenic non-protein coding RNA 1143 [Source:HGNC Symbol;Acc:HGNC:49458]"}, {"versioned_ensembl_gene_id":"ENSG00000237469.2","gene_symbol":"TUBB8P10","gene_name":"tubulin beta 8 class VIII pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42348]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391171","summary":null,"start":227493029,"end":227495142,"strand":-1,"description":"tubulin beta 8 class VIII pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42348]"}, {"versioned_ensembl_gene_id":"ENSG00000230013.1","gene_symbol":"AL359182.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104990796,"end":104991781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230148.8","gene_symbol":"HOXB-AS1","gene_name":"HOXB cluster antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43744]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874362","summary":null,"start":48543551,"end":48551250,"strand":1,"description":"HOXB cluster antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43744]"}, {"versioned_ensembl_gene_id":"ENSG00000122970.15","gene_symbol":"IFT81","gene_name":"intraflagellar transport 81 [Source:HGNC Symbol;Acc:HGNC:14313]","synonyms":"MGC4027,CDV1,CDV-1R","biotype":"protein_coding","ncbi_id":"28981","summary":"The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]","start":110124335,"end":110218797,"strand":1,"description":"intraflagellar transport 81 [Source:HGNC Symbol;Acc:HGNC:14313]"}, {"versioned_ensembl_gene_id":"ENSG00000080031.9","gene_symbol":"PTPRH","gene_name":"protein tyrosine phosphatase, receptor type H [Source:HGNC Symbol;Acc:HGNC:9672]","synonyms":"SAP-1","biotype":"protein_coding","ncbi_id":"5794","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. The extracellular region contains eight fibronectin type III-like repeats and multiple N-glycosylation sites. The gene was shown to be expressed primarily in brain and liver, and at a lower level in heart and stomach. It was also found to be expressed in several cancer cell lines, but not in the corresponding normal tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]","start":55181248,"end":55209506,"strand":-1,"description":"protein tyrosine phosphatase, receptor type H [Source:HGNC Symbol;Acc:HGNC:9672]"}, {"versioned_ensembl_gene_id":"ENSG00000227964.1","gene_symbol":"LINC01429","gene_name":"long intergenic non-protein coding RNA 1429 [Source:HGNC Symbol;Acc:HGNC:50741]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927678","summary":null,"start":51831797,"end":51862912,"strand":-1,"description":"long intergenic non-protein coding RNA 1429 [Source:HGNC Symbol;Acc:HGNC:50741]"}, {"versioned_ensembl_gene_id":"ENSG00000234050.1","gene_symbol":"Z95624.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102937770,"end":102940561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131746.12","gene_symbol":"TNS4","gene_name":"tensin 4 [Source:HGNC Symbol;Acc:HGNC:24352]","synonyms":"CTEN","biotype":"protein_coding","ncbi_id":"84951","summary":null,"start":40475828,"end":40501597,"strand":-1,"description":"tensin 4 [Source:HGNC Symbol;Acc:HGNC:24352]"}, {"versioned_ensembl_gene_id":"ENSG00000162004.16","gene_symbol":"CCDC78","gene_name":"coiled-coil domain containing 78 [Source:HGNC Symbol;Acc:HGNC:14153]","synonyms":"C16orf25,FLJ34512","biotype":"protein_coding","ncbi_id":"124093","summary":"The product of this gene contains two coiled-coil domains. The function of this gene is currently unknown. [provided by RefSeq, Sep 2012]","start":722582,"end":726954,"strand":-1,"description":"coiled-coil domain containing 78 [Source:HGNC Symbol;Acc:HGNC:14153]"}, {"versioned_ensembl_gene_id":"ENSG00000225101.5","gene_symbol":"OR52K3P","gene_name":"olfactory receptor family 52 subfamily K member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15224]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390035","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4469461,"end":4476407,"strand":1,"description":"olfactory receptor family 52 subfamily K member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15224]"}, {"versioned_ensembl_gene_id":"ENSG00000249163.3","gene_symbol":"AL121809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45083045,"end":45083977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278147.1","gene_symbol":"AL121809.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45079849,"end":45080189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250034.1","gene_symbol":"AC131956.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137807706,"end":137816402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104804.7","gene_symbol":"TULP2","gene_name":"tubby like protein 2 [Source:HGNC Symbol;Acc:HGNC:12424]","synonyms":"TUBL2,CT65","biotype":"protein_coding","ncbi_id":"7288","summary":"TULP2 is a member of a family of tubby-like genes (TULPs) that encode proteins of unknown function. Members of this family have been identified in plants, vertebrates, and invertebrates. The TULP proteins share a conserved C-terminal region of approximately 200 amino acid residues. [provided by RefSeq, Jul 2008]","start":48880965,"end":48898733,"strand":-1,"description":"tubby like protein 2 [Source:HGNC Symbol;Acc:HGNC:12424]"}, {"versioned_ensembl_gene_id":"ENSG00000255332.7","gene_symbol":"AP003028.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91794362,"end":91812294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280352.1","gene_symbol":"AC116563.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":137601899,"end":137602433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235736.1","gene_symbol":"AL031275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168763365,"end":168774490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141338.13","gene_symbol":"ABCA8","gene_name":"ATP binding cassette subfamily A member 8 [Source:HGNC Symbol;Acc:HGNC:38]","synonyms":"KIAA0822","biotype":"protein_coding","ncbi_id":"10351","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The encoded protein may regulate lipid metabolism and be involved in the formation and maintenance of myelin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":68867292,"end":68955392,"strand":-1,"description":"ATP binding cassette subfamily A member 8 [Source:HGNC Symbol;Acc:HGNC:38]"}, {"versioned_ensembl_gene_id":"ENSG00000234637.1","gene_symbol":"RPS19P6","gene_name":"ribosomal protein S19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36217]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271078","summary":null,"start":80782338,"end":80782770,"strand":-1,"description":"ribosomal protein S19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36217]"}, {"versioned_ensembl_gene_id":"ENSG00000231272.1","gene_symbol":"AL122008.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":234261706,"end":234274465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227789.1","gene_symbol":"MTCYBP7","gene_name":"mitochondrially encoded cytochrome b pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51964]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075257","summary":null,"start":82818131,"end":82819264,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51964]"}, {"versioned_ensembl_gene_id":"ENSG00000225901.1","gene_symbol":"MTND2P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42110]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100884155","summary":null,"start":80565032,"end":80565962,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42110]"}, {"versioned_ensembl_gene_id":"ENSG00000250040.2","gene_symbol":"RAF1P1","gene_name":"RAF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9830]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"348910","summary":null,"start":10254926,"end":10256621,"strand":-1,"description":"RAF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9830]"}, {"versioned_ensembl_gene_id":"ENSG00000232981.1","gene_symbol":"MTCO1P51","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:52116]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287067","summary":null,"start":80563571,"end":80564630,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:52116]"}, {"versioned_ensembl_gene_id":"ENSG00000236244.1","gene_symbol":"AL122008.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234268583,"end":234272500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231749.3","gene_symbol":"ABCA9-AS1","gene_name":"ABCA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39983]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355297","summary":null,"start":68944531,"end":69042784,"strand":1,"description":"ABCA9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39983]"}, {"versioned_ensembl_gene_id":"ENSG00000232494.1","gene_symbol":"AL161912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79874696,"end":79886678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253733.3","gene_symbol":"LZTS1-AS1","gene_name":"LZTS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43630]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874051","summary":null,"start":20275773,"end":20290458,"strand":1,"description":"LZTS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43630]"}, {"versioned_ensembl_gene_id":"ENSG00000229403.1","gene_symbol":"AC005999.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51614251,"end":51630870,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117477.12","gene_symbol":"CCDC181","gene_name":"coiled-coil domain containing 181 [Source:HGNC Symbol;Acc:HGNC:28051]","synonyms":"FLJ25846,C1orf114","biotype":"protein_coding","ncbi_id":"57821","summary":null,"start":169394870,"end":169460669,"strand":-1,"description":"coiled-coil domain containing 181 [Source:HGNC Symbol;Acc:HGNC:28051]"}, {"versioned_ensembl_gene_id":"ENSG00000228897.1","gene_symbol":"AC012441.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51386363,"end":51387101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129990.14","gene_symbol":"SYT5","gene_name":"synaptotagmin 5 [Source:HGNC Symbol;Acc:HGNC:11513]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6861","summary":"Synaptotagmins, such as SYT5, are a family of type III membrane proteins characterized by cytoplasmic repeats related to protein kinase C (see MIM 176960) regulatory (C2) domains, which are thought to bind calcium. Synaptotagmins may act both as negative regulators of vesicle fusion, allowing fusion in the presence of calcium, and as calcium receptors or sensor molecules (summary by Hudson and Birnbaum, 1995 [PubMed 7597049]).[supplied by OMIM, Feb 2011]","start":55171199,"end":55180441,"strand":-1,"description":"synaptotagmin 5 [Source:HGNC Symbol;Acc:HGNC:11513]"}, {"versioned_ensembl_gene_id":"ENSG00000243287.2","gene_symbol":"AP002088.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108378831,"end":108379545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283631.1","gene_symbol":"AL928596.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20311838,"end":20317783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236447.2","gene_symbol":"ATG10-IT1","gene_name":"ATG10 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41455]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874311","summary":null,"start":81991995,"end":81992481,"strand":1,"description":"ATG10 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41455]"}, {"versioned_ensembl_gene_id":"ENSG00000255074.1","gene_symbol":"AC018523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14440787,"end":14441677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265939.1","gene_symbol":"AC091147.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22900486,"end":22900995,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234720.3","gene_symbol":"ATP5A1P8","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37666]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392322","summary":null,"start":39654241,"end":39655531,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37666]"}, {"versioned_ensembl_gene_id":"ENSG00000186468.12","gene_symbol":"RPS23","gene_name":"ribosomal protein S23 [Source:HGNC Symbol;Acc:HGNC:10410]","synonyms":"S23","biotype":"protein_coding","ncbi_id":"6228","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S12P family of ribosomal proteins. It is located in the cytoplasm. The protein shares significant amino acid similarity with S. cerevisiae ribosomal protein S28. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":82273358,"end":82278577,"strand":-1,"description":"ribosomal protein S23 [Source:HGNC Symbol;Acc:HGNC:10410]"}, {"versioned_ensembl_gene_id":"ENSG00000271976.1","gene_symbol":"AC012467.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53858994,"end":53861576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123838.10","gene_symbol":"C4BPA","gene_name":"complement component 4 binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1325]","synonyms":"C4BP","biotype":"protein_coding","ncbi_id":"722","summary":"This gene encodes a member of a superfamily of proteins composed predominantly of tandemly arrayed short consensus repeats of approximately 60 amino acids. Along with a single, unique beta-chain, seven identical alpha-chains encoded by this gene assemble into the predominant isoform of C4b-binding protein, a multimeric protein that controls activation of the complement cascade through the classical pathway. The genes encoding both alpha and beta chains are located adjacent to each other on human chromosome 1 in the regulator of complement activation gene cluster. Two pseudogenes of this gene are also found in the cluster. [provided by RefSeq, Jul 2008]","start":207104262,"end":207144972,"strand":1,"description":"complement component 4 binding protein alpha [Source:HGNC Symbol;Acc:HGNC:1325]"}, {"versioned_ensembl_gene_id":"ENSG00000267640.6","gene_symbol":"AC016582.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37817359,"end":37832160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228316.1","gene_symbol":"MTATP6P19","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52064]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075275","summary":null,"start":102798396,"end":102799560,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52064]"}, {"versioned_ensembl_gene_id":"ENSG00000242248.2","gene_symbol":"RPL7AP57","gene_name":"ribosomal protein L7a pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:36551]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271537","summary":null,"start":92161106,"end":92161889,"strand":1,"description":"ribosomal protein L7a pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:36551]"}, {"versioned_ensembl_gene_id":"ENSG00000224244.1","gene_symbol":"AC073508.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40687038,"end":40689360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233405.1","gene_symbol":"LINC01046","gene_name":"long intergenic non-protein coding RNA 1046 [Source:HGNC Symbol;Acc:HGNC:49040]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103689843","summary":null,"start":21234568,"end":21235204,"strand":1,"description":"long intergenic non-protein coding RNA 1046 [Source:HGNC Symbol;Acc:HGNC:49040]"}, {"versioned_ensembl_gene_id":"ENSG00000278859.1","gene_symbol":"AP002799.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91992833,"end":91993255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134532.15","gene_symbol":"SOX5","gene_name":"SRY-box 5 [Source:HGNC Symbol;Acc:HGNC:11201]","synonyms":"MGC35153,L-SOX5","biotype":"protein_coding","ncbi_id":"6660","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":23529500,"end":23951032,"strand":-1,"description":"SRY-box 5 [Source:HGNC Symbol;Acc:HGNC:11201]"}, {"versioned_ensembl_gene_id":"ENSG00000197044.10","gene_symbol":"ZNF441","gene_name":"zinc finger protein 441 [Source:HGNC Symbol;Acc:HGNC:20875]","synonyms":"FLJ38637","biotype":"protein_coding","ncbi_id":"126068","summary":null,"start":11767000,"end":11784078,"strand":1,"description":"zinc finger protein 441 [Source:HGNC Symbol;Acc:HGNC:20875]"}, {"versioned_ensembl_gene_id":"ENSG00000114686.8","gene_symbol":"MRPL3","gene_name":"mitochondrial ribosomal protein L3 [Source:HGNC Symbol;Acc:HGNC:10379]","synonyms":"RPML3,MRL3","biotype":"protein_coding","ncbi_id":"11222","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L3P ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 13q. [provided by RefSeq, Jul 2008]","start":131462212,"end":131502983,"strand":-1,"description":"mitochondrial ribosomal protein L3 [Source:HGNC Symbol;Acc:HGNC:10379]"}, {"versioned_ensembl_gene_id":"ENSG00000173728.10","gene_symbol":"C1orf100","gene_name":"chromosome 1 open reading frame 100 [Source:HGNC Symbol;Acc:HGNC:30435]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200159","summary":null,"start":244352635,"end":244389663,"strand":1,"description":"chromosome 1 open reading frame 100 [Source:HGNC Symbol;Acc:HGNC:30435]"}, {"versioned_ensembl_gene_id":"ENSG00000148248.13","gene_symbol":"SURF4","gene_name":"surfeit 4 [Source:HGNC Symbol;Acc:HGNC:11476]","synonyms":"MGC102753,FLJ22993,ERV29","biotype":"protein_coding","ncbi_id":"6836","summary":"This gene is located in the surfeit gene cluster, which is comprised of very tightly linked housekeeping genes that do not share sequence similarity. The encoded protein is a conserved integral membrane protein that interacts with endoplasmic reticulum-Golgi intermediate compartment proteins. Disruption of this gene results in reduced numbers of endoplasmic reticulum-Golgi intermediate compartment clusters and redistribution of coat protein I to the cytosol. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133361449,"end":133376166,"strand":-1,"description":"surfeit 4 [Source:HGNC Symbol;Acc:HGNC:11476]"}, {"versioned_ensembl_gene_id":"ENSG00000277866.1","gene_symbol":"AC022106.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":150978419,"end":150979175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280407.2","gene_symbol":"AC132872.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82249067,"end":82251844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275888.1","gene_symbol":"AC132872.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82244770,"end":82245591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000035687.9","gene_symbol":"ADSS","gene_name":"adenylosuccinate synthase [Source:HGNC Symbol;Acc:HGNC:292]","synonyms":null,"biotype":"protein_coding","ncbi_id":"159","summary":"This gene encodes the enzyme adenylosuccinate synthetase which catalyzes the first committed step in the conversion of inosine monophosphate to adenosine monophosphate. A pseudogene of this gene is found on chromosome 17.[provided by RefSeq, Nov 2010]","start":244408494,"end":244452134,"strand":-1,"description":"adenylosuccinate synthase [Source:HGNC Symbol;Acc:HGNC:292]"}, {"versioned_ensembl_gene_id":"ENSG00000256235.1","gene_symbol":"SMIM3","gene_name":"small integral membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:30248]","synonyms":"NID67,MSTP150,C5orf62","biotype":"protein_coding","ncbi_id":"85027","summary":null,"start":150777946,"end":150796734,"strand":1,"description":"small integral membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:30248]"}, {"versioned_ensembl_gene_id":"ENSG00000113722.16","gene_symbol":"CDX1","gene_name":"caudal type homeobox 1 [Source:HGNC Symbol;Acc:HGNC:1805]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1044","summary":"This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded DNA-binding protein regulates intestine-specific gene expression and enterocyte differentiation. It has been shown to induce expression of the intestinal alkaline phosphatase gene, and inhibit beta-catenin/T-cell factor transcriptional activity. [provided by RefSeq, Jul 2008]","start":150166795,"end":150184558,"strand":1,"description":"caudal type homeobox 1 [Source:HGNC Symbol;Acc:HGNC:1805]"}, {"versioned_ensembl_gene_id":"ENSG00000230303.5","gene_symbol":"AL353743.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85785722,"end":85793480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224020.1","gene_symbol":"MIR181A2HG","gene_name":"MIR181A2 host gene [Source:HGNC Symbol;Acc:HGNC:37188]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100379345","summary":null,"start":124658467,"end":124698631,"strand":1,"description":"MIR181A2 host gene [Source:HGNC Symbol;Acc:HGNC:37188]"}, {"versioned_ensembl_gene_id":"ENSG00000203837.4","gene_symbol":"PNLIPRP3","gene_name":"pancreatic lipase related protein 3 [Source:HGNC Symbol;Acc:HGNC:23492]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119548","summary":null,"start":116427867,"end":116477957,"strand":1,"description":"pancreatic lipase related protein 3 [Source:HGNC Symbol;Acc:HGNC:23492]"}, {"versioned_ensembl_gene_id":"ENSG00000164330.16","gene_symbol":"EBF1","gene_name":"early B-cell factor 1 [Source:HGNC Symbol;Acc:HGNC:3126]","synonyms":"OLF1,EBF","biotype":"protein_coding","ncbi_id":"1879","summary":null,"start":158695916,"end":159099761,"strand":-1,"description":"early B-cell factor 1 [Source:HGNC Symbol;Acc:HGNC:3126]"}, {"versioned_ensembl_gene_id":"ENSG00000141526.16","gene_symbol":"SLC16A3","gene_name":"solute carrier family 16 member 3 [Source:HGNC Symbol;Acc:HGNC:10924]","synonyms":"MCT4,MCT3","biotype":"protein_coding","ncbi_id":"9123","summary":"Lactic acid and pyruvate transport across plasma membranes is catalyzed by members of the proton-linked monocarboxylate transporter (MCT) family, which has been designated solute carrier family-16. Each MCT appears to have slightly different substrate and inhibitor specificities and transport kinetics, which are related to the metabolic requirements of the tissues in which it is found. The MCTs, which include MCT1 (SLC16A1; MIM 600682) and MCT2 (SLC16A7; MIM 603654), are characterized by 12 predicted transmembrane domains (Price et al., 1998 [PubMed 9425115]).[supplied by OMIM, Mar 2008]","start":82228397,"end":82261129,"strand":1,"description":"solute carrier family 16 member 3 [Source:HGNC Symbol;Acc:HGNC:10924]"}, {"versioned_ensembl_gene_id":"ENSG00000253456.1","gene_symbol":"AC136424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158985806,"end":158987199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232132.1","gene_symbol":"NDFIP2-AS1","gene_name":"NDFIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40844]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874208","summary":null,"start":79477364,"end":79481231,"strand":-1,"description":"NDFIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40844]"}, {"versioned_ensembl_gene_id":"ENSG00000189430.12","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335,NKP46","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54906150,"end":54916140,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000273445.1","gene_symbol":"AC133644.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87477495,"end":87478034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279255.1","gene_symbol":"Z97653.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":707650,"end":709067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222011.8","gene_symbol":"FAM185A","gene_name":"family with sequence similarity 185 member A [Source:HGNC Symbol;Acc:HGNC:22412]","synonyms":"MGC35361","biotype":"protein_coding","ncbi_id":"222234","summary":null,"start":102748971,"end":102809225,"strand":1,"description":"family with sequence similarity 185 member A [Source:HGNC Symbol;Acc:HGNC:22412]"}, {"versioned_ensembl_gene_id":"ENSG00000230584.1","gene_symbol":"CCT5P2","gene_name":"chaperonin containing TCP1 subunit 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390415","summary":null,"start":78908919,"end":78910542,"strand":1,"description":"chaperonin containing TCP1 subunit 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35139]"}, {"versioned_ensembl_gene_id":"ENSG00000282007.1","gene_symbol":"TRBV10-2","gene_name":"T-cell receptor beta variable 10-2 [Source:HGNC Symbol;Acc:HGNC:12178]","synonyms":"TRBV102,TCRBV12S3,TCRBV10S2","biotype":"TR_V_gene","ncbi_id":"28584","summary":null,"start":142446652,"end":142447152,"strand":1,"description":"T-cell receptor beta variable 10-2 [Source:HGNC Symbol;Acc:HGNC:12178]"}, {"versioned_ensembl_gene_id":"ENSG00000279625.1","gene_symbol":"AL591122.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":22364630,"end":22366482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275764.1","gene_symbol":"AC092747.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27037100,"end":27038960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166479.9","gene_symbol":"TMX3","gene_name":"thioredoxin related transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:24718]","synonyms":"TXNDC10,PDIA13,KIAA1830,FLJ20793","biotype":"protein_coding","ncbi_id":"54495","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The canonical protein encoded by this gene has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, one transmembrane domain and a C-terminal ER-retention sequence. This gene is expressed in many tissues but has its highest expression in heart and skeletal muscle. It is expressed in the retinal neuroepithelium and lens epithelium in the developing murine eye and haploinsufficiency of this gene in humans and zebrafish is associated with microphthalmia. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]","start":68673688,"end":68715298,"strand":-1,"description":"thioredoxin related transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:24718]"}, {"versioned_ensembl_gene_id":"ENSG00000263637.1","gene_symbol":"AC022035.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68753179,"end":68754583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158301.18","gene_symbol":"GPRASP2","gene_name":"G protein-coupled receptor associated sorting protein 2 [Source:HGNC Symbol;Acc:HGNC:25169]","synonyms":"GASP2,FLJ37327","biotype":"protein_coding","ncbi_id":"114928","summary":"The protein encoded by this gene is a member of a family that regulates the activity of G protein-coupled receptors (GPCRs). The encoded protein has been shown to be capable of interacting with several GPCRs, including the M1 muscarinic acetylcholine receptor and the calcitonin receptor. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]","start":102712176,"end":102717733,"strand":1,"description":"G protein-coupled receptor associated sorting protein 2 [Source:HGNC Symbol;Acc:HGNC:25169]"}, {"versioned_ensembl_gene_id":"ENSG00000214837.8","gene_symbol":"LINC01347","gene_name":"long intergenic non-protein coding RNA 1347 [Source:HGNC Symbol;Acc:HGNC:50566]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"731275","summary":null,"start":243056307,"end":243101744,"strand":-1,"description":"long intergenic non-protein coding RNA 1347 [Source:HGNC Symbol;Acc:HGNC:50566]"}, {"versioned_ensembl_gene_id":"ENSG00000140067.6","gene_symbol":"FAM181A","gene_name":"family with sequence similarity 181 member A [Source:HGNC Symbol;Acc:HGNC:20491]","synonyms":"C14orf152","biotype":"protein_coding","ncbi_id":"90050","summary":null,"start":93918894,"end":93929608,"strand":1,"description":"family with sequence similarity 181 member A [Source:HGNC Symbol;Acc:HGNC:20491]"}, {"versioned_ensembl_gene_id":"ENSG00000235514.1","gene_symbol":"LLPHP2","gene_name":"LLP homolog, long-term synaptic facilitation pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50492]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480300","summary":null,"start":25762938,"end":25763333,"strand":-1,"description":"LLP homolog, long-term synaptic facilitation pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50492]"}, {"versioned_ensembl_gene_id":"ENSG00000274154.1","gene_symbol":"AC114781.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83369416,"end":83369523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206527.9","gene_symbol":"HACD2","gene_name":"3-hydroxyacyl-CoA dehydratase 2 [Source:HGNC Symbol;Acc:HGNC:9640]","synonyms":"PTPLB","biotype":"protein_coding","ncbi_id":"201562","summary":"The protein encoded by this gene can catalyze the third step (dehydration) in the conversion of long chain fatty acids to very long chain fatty acids. The encoded protein localizes to the endoplasmic reticulum membrane. [provided by RefSeq, Jul 2016]","start":123490820,"end":123585185,"strand":-1,"description":"3-hydroxyacyl-CoA dehydratase 2 [Source:HGNC Symbol;Acc:HGNC:9640]"}, {"versioned_ensembl_gene_id":"ENSG00000279500.1","gene_symbol":"AC108704.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":128813186,"end":128814750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264421.1","gene_symbol":"AC007448.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67224303,"end":67225541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264093.1","gene_symbol":"AC007448.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67276118,"end":67276351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254965.1","gene_symbol":"C1DP5","gene_name":"C1D nuclear receptor corepressor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51613]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481729","summary":null,"start":83111060,"end":83111442,"strand":-1,"description":"C1D nuclear receptor corepressor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51613]"}, {"versioned_ensembl_gene_id":"ENSG00000224792.6","gene_symbol":"IQCF4","gene_name":"IQ motif containing F5 pseudogene [Source:NCBI gene;Acc:100506840]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100506840","summary":null,"start":51817603,"end":51819635,"strand":1,"description":"IQ motif containing F5 pseudogene [Source:NCBI gene;Acc:100506840]"}, {"versioned_ensembl_gene_id":"ENSG00000231149.2","gene_symbol":"AL354979.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124514938,"end":124516056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260578.1","gene_symbol":"AC110597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67481791,"end":67484966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237452.2","gene_symbol":"BHMG1","gene_name":"basic helix-loop-helix and HMG-box containing 1 [Source:HGNC Symbol;Acc:HGNC:44318]","synonyms":"HMGDC","biotype":"protein_coding","ncbi_id":"388553","summary":null,"start":45733251,"end":45764534,"strand":1,"description":"basic helix-loop-helix and HMG-box containing 1 [Source:HGNC Symbol;Acc:HGNC:44318]"}, {"versioned_ensembl_gene_id":"ENSG00000175785.12","gene_symbol":"PRIMA1","gene_name":"proline rich membrane anchor 1 [Source:HGNC Symbol;Acc:HGNC:18319]","synonyms":"PRIMA","biotype":"protein_coding","ncbi_id":"145270","summary":"The product of this gene functions to organize acetylcholinesterase (AChE) into tetramers, and to anchor AChE at neural cell membranes. [provided by RefSeq, Nov 2008]","start":93718298,"end":93788481,"strand":-1,"description":"proline rich membrane anchor 1 [Source:HGNC Symbol;Acc:HGNC:18319]"}, {"versioned_ensembl_gene_id":"ENSG00000213064.9","gene_symbol":"SFT2D2","gene_name":"SFT2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25140]","synonyms":"UNQ512,dJ747L4.C1.2","biotype":"protein_coding","ncbi_id":"375035","summary":null,"start":168225938,"end":168253025,"strand":1,"description":"SFT2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25140]"}, {"versioned_ensembl_gene_id":"ENSG00000124466.8","gene_symbol":"LYPD3","gene_name":"LY6/PLAUR domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24880]","synonyms":"C4.4A","biotype":"protein_coding","ncbi_id":"27076","summary":null,"start":43460787,"end":43465660,"strand":-1,"description":"LY6/PLAUR domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24880]"}, {"versioned_ensembl_gene_id":"ENSG00000027869.11","gene_symbol":"SH2D2A","gene_name":"SH2 domain containing 2A [Source:HGNC Symbol;Acc:HGNC:10821]","synonyms":"TSAd,F2771","biotype":"protein_coding","ncbi_id":"9047","summary":"This gene encodes an adaptor protein thought to function in T-cell signal transduction. A related protein in mouse is responsible for the activation of lymphocyte-specific protein-tyrosine kinase and functions in downstream signaling. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":156806243,"end":156816862,"strand":-1,"description":"SH2 domain containing 2A [Source:HGNC Symbol;Acc:HGNC:10821]"}, {"versioned_ensembl_gene_id":"ENSG00000054793.13","gene_symbol":"ATP9A","gene_name":"ATPase phospholipid transporting 9A (putative) [Source:HGNC Symbol;Acc:HGNC:13540]","synonyms":"KIAA0611,ATPIIA","biotype":"protein_coding","ncbi_id":"10079","summary":null,"start":51596514,"end":51768634,"strand":-1,"description":"ATPase phospholipid transporting 9A (putative) [Source:HGNC Symbol;Acc:HGNC:13540]"}, {"versioned_ensembl_gene_id":"ENSG00000242111.1","gene_symbol":"TOPORSLP1","gene_name":"topoisomerase I binding, arginine and serine rich like, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50276]","synonyms":"TOPORSLP","biotype":"transcribed_unitary_pseudogene","ncbi_id":"347281","summary":null,"start":104270228,"end":104286955,"strand":1,"description":"topoisomerase I binding, arginine and serine rich like, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50276]"}, {"versioned_ensembl_gene_id":"ENSG00000109667.11","gene_symbol":"SLC2A9","gene_name":"solute carrier family 2 member 9 [Source:HGNC Symbol;Acc:HGNC:13446]","synonyms":"URATv1,GLUTX,Glut9","biotype":"protein_coding","ncbi_id":"56606","summary":"This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":9771153,"end":10054936,"strand":-1,"description":"solute carrier family 2 member 9 [Source:HGNC Symbol;Acc:HGNC:13446]"}, {"versioned_ensembl_gene_id":"ENSG00000204933.3","gene_symbol":"CD177P1","gene_name":"CD177 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34508]","synonyms":"CD177P","biotype":"unprocessed_pseudogene","ncbi_id":"653579","summary":null,"start":43372742,"end":43379123,"strand":-1,"description":"CD177 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34508]"}, {"versioned_ensembl_gene_id":"ENSG00000226670.1","gene_symbol":"BCAS2P3","gene_name":"BCAS2, pre-mRNA processing factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128339","summary":null,"start":79166119,"end":79166885,"strand":1,"description":"BCAS2, pre-mRNA processing factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39596]"}, {"versioned_ensembl_gene_id":"ENSG00000144021.2","gene_symbol":"CIAO1","gene_name":"cytosolic iron-sulfur assembly component 1 [Source:HGNC Symbol;Acc:HGNC:14280]","synonyms":"WDR39,CIA1","biotype":"protein_coding","ncbi_id":"9391","summary":null,"start":96266132,"end":96273349,"strand":1,"description":"cytosolic iron-sulfur assembly component 1 [Source:HGNC Symbol;Acc:HGNC:14280]"}, {"versioned_ensembl_gene_id":"ENSG00000196465.10","gene_symbol":"MYL6B","gene_name":"myosin light chain 6B [Source:HGNC Symbol;Acc:HGNC:29823]","synonyms":"MLC1SA","biotype":"protein_coding","ncbi_id":"140465","summary":"Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in both slow-twitch skeletal muscle and in nonmuscle tissue. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":56152256,"end":56159647,"strand":1,"description":"myosin light chain 6B [Source:HGNC Symbol;Acc:HGNC:29823]"}, {"versioned_ensembl_gene_id":"ENSG00000176809.10","gene_symbol":"LRRC37A3","gene_name":"leucine rich repeat containing 37 member A3 [Source:HGNC Symbol;Acc:HGNC:32427]","synonyms":"KIAA0563,FLJ34306","biotype":"protein_coding","ncbi_id":"374819","summary":null,"start":64854312,"end":64919480,"strand":-1,"description":"leucine rich repeat containing 37 member A3 [Source:HGNC Symbol;Acc:HGNC:32427]"}, {"versioned_ensembl_gene_id":"ENSG00000171169.8","gene_symbol":"NAIF1","gene_name":"nuclear apoptosis inducing factor 1 [Source:HGNC Symbol;Acc:HGNC:25446]","synonyms":"DKFZp762G199,C9orf90,bA379C10.2","biotype":"protein_coding","ncbi_id":"203245","summary":null,"start":128061233,"end":128068206,"strand":-1,"description":"nuclear apoptosis inducing factor 1 [Source:HGNC Symbol;Acc:HGNC:25446]"}, {"versioned_ensembl_gene_id":"ENSG00000272400.1","gene_symbol":"AC103810.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64847386,"end":64847728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270521.1","gene_symbol":"AL450336.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66710242,"end":66710827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279249.1","gene_symbol":"AC007614.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49341663,"end":49350554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185482.7","gene_symbol":"STAC3","gene_name":"SH3 and cysteine rich domain 3 [Source:HGNC Symbol;Acc:HGNC:28423]","synonyms":"MGC2793","biotype":"protein_coding","ncbi_id":"246329","summary":"The protein encoded by this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided by RefSeq, Nov 2013]","start":57243453,"end":57251193,"strand":-1,"description":"SH3 and cysteine rich domain 3 [Source:HGNC Symbol;Acc:HGNC:28423]"}, {"versioned_ensembl_gene_id":"ENSG00000228278.3","gene_symbol":"ORM2","gene_name":"orosomucoid 2 [Source:HGNC Symbol;Acc:HGNC:8499]","synonyms":"AGP2,AGP-B',AGP-B","biotype":"protein_coding","ncbi_id":"5005","summary":"This gene encodes a key acute phase plasma protein. Because of its increase due to acute inflammation, this protein is classified as an acute-phase reactant. The specific function of this protein has not yet been determined; however, it may be involved in aspects of immunosuppression. [provided by RefSeq, Jul 2008]","start":114329869,"end":114333252,"strand":1,"description":"orosomucoid 2 [Source:HGNC Symbol;Acc:HGNC:8499]"}, {"versioned_ensembl_gene_id":"ENSG00000215769.8","gene_symbol":"ARHGAP27P1-BPTFP1-KPNA2P3","gene_name":"ARHGAP27P1-BPTFP1-KPNA2P3 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:52873]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"109286553","summary":"This locus represents naturally-occurring readthrough transcription between multiple unprocessed pseudogene loci. Readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Dec 2016]","start":64749663,"end":64781707,"strand":-1,"description":"ARHGAP27P1-BPTFP1-KPNA2P3 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:52873]"}, {"versioned_ensembl_gene_id":"ENSG00000130829.17","gene_symbol":"DUSP9","gene_name":"dual specificity phosphatase 9 [Source:HGNC Symbol;Acc:HGNC:3076]","synonyms":"MKP4,MKP-4","biotype":"protein_coding","ncbi_id":"1852","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product shows selectivity for members of the ERK family of MAP kinases and is localized to the cytoplasm and nucleus. Aberrant expression of this gene is associated with type 2 diabetes and cancer progression in several cell types. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":153642492,"end":153651326,"strand":1,"description":"dual specificity phosphatase 9 [Source:HGNC Symbol;Acc:HGNC:3076]"}, {"versioned_ensembl_gene_id":"ENSG00000265982.1","gene_symbol":"AC103810.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64778842,"end":64778937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231259.4","gene_symbol":"AC125232.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87031815,"end":87053069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244086.1","gene_symbol":"AC110749.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38855314,"end":38855670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211880.1","gene_symbol":"TRAJ9","gene_name":"T-cell receptor alpha joining 9 [Source:HGNC Symbol;Acc:HGNC:12097]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28746","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22535554,"end":22535614,"strand":1,"description":"T-cell receptor alpha joining 9 [Source:HGNC Symbol;Acc:HGNC:12097]"}, {"versioned_ensembl_gene_id":"ENSG00000230108.3","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31566312,"end":31569081,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000236062.1","gene_symbol":"GSTM5P1","gene_name":"glutathione S-transferase mu 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4633]","synonyms":"GSTM1L,GST1L","biotype":"processed_pseudogene","ncbi_id":"100505557","summary":null,"start":12257801,"end":12258460,"strand":-1,"description":"glutathione S-transferase mu 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4633]"}, {"versioned_ensembl_gene_id":"ENSG00000211879.1","gene_symbol":"TRAJ10","gene_name":"T-cell receptor alpha joining 10 [Source:HGNC Symbol;Acc:HGNC:12038]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28745","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22533497,"end":22533560,"strand":1,"description":"T-cell receptor alpha joining 10 [Source:HGNC Symbol;Acc:HGNC:12038]"}, {"versioned_ensembl_gene_id":"ENSG00000132383.11","gene_symbol":"RPA1","gene_name":"replication protein A1 [Source:HGNC Symbol;Acc:HGNC:10289]","synonyms":"HSSB,RPA70,RP-A,RF-A,REPA1","biotype":"protein_coding","ncbi_id":"6117","summary":"This gene encodes the largest subunit of the heterotrimeric Replication Protein A (RPA) complex, which binds to single-stranded DNA (ssDNA), forming a nucleoprotein complex that plays an important role in DNA metabolism, being involved in DNA replication, repair, recombination, telomere maintenance, and co-ordinating the cellular response to DNA damage through activation of the ataxia telangiectasia and Rad3-related protein (ATR) kinase. The nucleoprotein complex protects the single-stranded DNA from nucleases, prevents formation of secondary structures that would interfere with repair, and co-ordinates the recruitment and departure of different genome maintenance factors. This subunit contains four oligonucleotide/oligosaccharide-binding (OB) domains, though the majority of ssDNA binding occurs in two of these domains. The heterotrimeric complex has two different modes of ssDNA binding, a low-affinity and high-affinity mode, determined by which ssDNA binding domains are utilized. The different binding modes differ in the length of DNA bound and in the proteins with which it interacts, thereby playing a role in regulating different genomic maintenance pathways. [provided by RefSeq, Sep 2017]","start":1829702,"end":1900082,"strand":1,"description":"replication protein A1 [Source:HGNC Symbol;Acc:HGNC:10289]"}, {"versioned_ensembl_gene_id":"ENSG00000174669.11","gene_symbol":"SLC29A2","gene_name":"solute carrier family 29 member 2 [Source:HGNC Symbol;Acc:HGNC:11004]","synonyms":"HNP36,ENT2,DER12","biotype":"protein_coding","ncbi_id":"3177","summary":"The uptake of nucleosides by transporters, such as SLC29A2, is essential for nucleotide synthesis by salvage pathways in cells that lack de novo biosynthetic pathways. Nucleoside transport also plays a key role in the regulation of many physiologic processes through its effect on adenosine concentration at the cell surface (Griffiths et al., 1997 [PubMed 9396714]).[supplied by OMIM, Nov 2008]","start":66362521,"end":66372214,"strand":-1,"description":"solute carrier family 29 member 2 [Source:HGNC Symbol;Acc:HGNC:11004]"}, {"versioned_ensembl_gene_id":"ENSG00000276203.4","gene_symbol":"ANKRD20A3","gene_name":"ankyrin repeat domain 20 family member A3 [Source:HGNC Symbol;Acc:HGNC:31981]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441425","summary":null,"start":66106815,"end":66153135,"strand":-1,"description":"ankyrin repeat domain 20 family member A3 [Source:HGNC Symbol;Acc:HGNC:31981]"}, {"versioned_ensembl_gene_id":"ENSG00000260635.1","gene_symbol":"AC092338.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22365121,"end":22369047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119772.16","gene_symbol":"DNMT3A","gene_name":"DNA methyltransferase 3 alpha [Source:HGNC Symbol;Acc:HGNC:2978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1788","summary":"CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase that is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes to the cytoplasm and nucleus and its expression is developmentally regulated. [provided by RefSeq, Mar 2016]","start":25227855,"end":25342590,"strand":-1,"description":"DNA methyltransferase 3 alpha [Source:HGNC Symbol;Acc:HGNC:2978]"}, {"versioned_ensembl_gene_id":"ENSG00000231412.2","gene_symbol":"AC005392.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43329295,"end":43331430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271820.1","gene_symbol":"AL109910.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170266669,"end":170276762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224765.1","gene_symbol":"AL035443.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137556191,"end":137564387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275496.4","gene_symbol":"CU633906.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6228966,"end":6267317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232394.1","gene_symbol":"AC090696.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27775621,"end":27776798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237675.5","gene_symbol":"TEX36-AS1","gene_name":"TEX36 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49500]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100169752","summary":null,"start":125574371,"end":125578445,"strand":1,"description":"TEX36 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49500]"}, {"versioned_ensembl_gene_id":"ENSG00000260184.1","gene_symbol":"AC023827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48849919,"end":48850015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135049.15","gene_symbol":"AGTPBP1","gene_name":"ATP/GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17258]","synonyms":"Nna1,KIAA1035,CCP1","biotype":"protein_coding","ncbi_id":"23287","summary":"NNA1 is a zinc carboxypeptidase that contains nuclear localization signals and an ATP/GTP-binding motif that was initially cloned from regenerating spinal cord neurons of the mouse.[supplied by OMIM, Jul 2002]","start":85546539,"end":85742029,"strand":-1,"description":"ATP/GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17258]"}, {"versioned_ensembl_gene_id":"ENSG00000166530.8","gene_symbol":"HSBP1P2","gene_name":"heat shock factor binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288483","summary":null,"start":110251871,"end":110252099,"strand":-1,"description":"heat shock factor binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37300]"}, {"versioned_ensembl_gene_id":"ENSG00000269483.2","gene_symbol":"AC006272.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51842878,"end":51843315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226428.1","gene_symbol":"RPL15P13","gene_name":"ribosomal protein L15 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131338","summary":null,"start":114900722,"end":114901366,"strand":1,"description":"ribosomal protein L15 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35915]"}, {"versioned_ensembl_gene_id":"ENSG00000283236.1","gene_symbol":"AC074141.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51860242,"end":51863236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205695.3","gene_symbol":"AL390205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139659928,"end":139661513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139324.11","gene_symbol":"TMTC3","gene_name":"transmembrane and tetratricopeptide repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:26899]","synonyms":"SMILE,FLJ90492","biotype":"protein_coding","ncbi_id":"160418","summary":"This gene encodes a protein that belongs to the transmembrane and tetratricopeptide repeat-containing protein family. [provided by RefSeq, May 2010]","start":88142296,"end":88199887,"strand":1,"description":"transmembrane and tetratricopeptide repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:26899]"}, {"versioned_ensembl_gene_id":"ENSG00000273036.3","gene_symbol":"AL390726.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":38540567,"end":38542792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279042.1","gene_symbol":"AP005242.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":14990707,"end":14993235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255060.1","gene_symbol":"AC009656.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36425447,"end":36426122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255186.1","gene_symbol":"AC087277.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36386521,"end":36388250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042286.14","gene_symbol":"AIFM2","gene_name":"apoptosis inducing factor, mitochondria associated 2 [Source:HGNC Symbol;Acc:HGNC:21411]","synonyms":"PRG3,FLJ14497,AMID","biotype":"protein_coding","ncbi_id":"84883","summary":"This gene encodes a flavoprotein oxidoreductase that binds single stranded DNA and is thought to contribute to apoptosis in the presence of bacterial and viral DNA. The expression of this gene is also found to be induced by tumor suppressor protein p53 in colon cancer cells. [provided by RefSeq, Nov 2010]","start":70098223,"end":70132934,"strand":-1,"description":"apoptosis inducing factor, mitochondria associated 2 [Source:HGNC Symbol;Acc:HGNC:21411]"}, {"versioned_ensembl_gene_id":"ENSG00000271474.1","gene_symbol":"AC106881.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95549129,"end":95552457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130816.14","gene_symbol":"DNMT1","gene_name":"DNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2976]","synonyms":"MCMT,DNMT,CXXC9","biotype":"protein_coding","ncbi_id":"1786","summary":"This gene encodes an enzyme that transfers methyl groups to cytosine nucleotides of genomic DNA. This protein is the major enzyme responsible for maintaining methylation patterns following DNA replication and shows a preference for hemi-methylated DNA. Methylation of DNA is an important component of mammalian epigenetic gene regulation. Aberrant methylation patterns are found in human tumors and associated with developmental abnormalities. Variation in this gene has been associated with cerebellar ataxia, deafness, and narcolepsy, and neuropathy, hereditary sensory, type IE. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":10133345,"end":10231286,"strand":-1,"description":"DNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2976]"}, {"versioned_ensembl_gene_id":"ENSG00000165379.13","gene_symbol":"LRFN5","gene_name":"leucine rich repeat and fibronectin type III domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20360]","synonyms":"SALM5,FIGLER8,C14orf146","biotype":"protein_coding","ncbi_id":"145581","summary":"This gene encodes a protein that belongs to the leucine-rich repeat and fibronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmembrane protein, is thought to function in presynaptic differentiation. [provided by RefSeq, Sep 2016]","start":41607570,"end":41904549,"strand":1,"description":"leucine rich repeat and fibronectin type III domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20360]"}, {"versioned_ensembl_gene_id":"ENSG00000197045.12","gene_symbol":"GMFB","gene_name":"glia maturation factor beta [Source:HGNC Symbol;Acc:HGNC:4373]","synonyms":"GMF","biotype":"protein_coding","ncbi_id":"2764","summary":null,"start":54474484,"end":54489196,"strand":-1,"description":"glia maturation factor beta [Source:HGNC Symbol;Acc:HGNC:4373]"}, {"versioned_ensembl_gene_id":"ENSG00000179676.6","gene_symbol":"LINC00305","gene_name":"long intergenic non-protein coding RNA 305 [Source:HGNC Symbol;Acc:HGNC:28597]","synonyms":"NCRNA00305,MGC39571,HsT1235,C18orf20","biotype":"lincRNA","ncbi_id":"221241","summary":null,"start":64080009,"end":64149030,"strand":-1,"description":"long intergenic non-protein coding RNA 305 [Source:HGNC Symbol;Acc:HGNC:28597]"}, {"versioned_ensembl_gene_id":"ENSG00000213533.11","gene_symbol":"TMEM110","gene_name":"transmembrane protein 110 [Source:HGNC Symbol;Acc:HGNC:30526]","synonyms":"MGC52022","biotype":"protein_coding","ncbi_id":"375346","summary":null,"start":52836219,"end":52897596,"strand":-1,"description":"transmembrane protein 110 [Source:HGNC Symbol;Acc:HGNC:30526]"}, {"versioned_ensembl_gene_id":"ENSG00000274664.1","gene_symbol":"AP005019.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72562044,"end":72562554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260171.1","gene_symbol":"AC008269.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206821190,"end":206822294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276109.1","gene_symbol":"AP005019.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72551049,"end":72551919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267134.1","gene_symbol":"LINC01924","gene_name":"long intergenic non-protein coding RNA 1924 [Source:HGNC Symbol;Acc:HGNC:27600]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284294","summary":null,"start":64104091,"end":64423601,"strand":1,"description":"long intergenic non-protein coding RNA 1924 [Source:HGNC Symbol;Acc:HGNC:27600]"}, {"versioned_ensembl_gene_id":"ENSG00000143590.13","gene_symbol":"EFNA3","gene_name":"ephrin A3 [Source:HGNC Symbol;Acc:HGNC:3223]","synonyms":"LERK3,EPLG3,Ehk1-L","biotype":"protein_coding","ncbi_id":"1944","summary":"This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNA class ephrin. [provided by RefSeq, Jul 2008]","start":155078872,"end":155087538,"strand":1,"description":"ephrin A3 [Source:HGNC Symbol;Acc:HGNC:3223]"}, {"versioned_ensembl_gene_id":"ENSG00000251246.1","gene_symbol":"AL691442.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":155063748,"end":155086807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228288.6","gene_symbol":"PCAT6","gene_name":"prostate cancer associated transcript 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43714]","synonyms":"PCAN-R1,onco-lncRNA-96,ncRNA-a2,KDM5BAS1,KDM5B-AS1","biotype":"antisense_RNA","ncbi_id":"100506696","summary":null,"start":202810954,"end":202812156,"strand":1,"description":"prostate cancer associated transcript 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43714]"}, {"versioned_ensembl_gene_id":"ENSG00000251363.2","gene_symbol":"LINC02315","gene_name":"long intergenic non-protein coding RNA 2315 [Source:HGNC Symbol;Acc:HGNC:53234]","synonyms":null,"biotype":"lincRNA","ncbi_id":"644919","summary":null,"start":40954898,"end":40975877,"strand":1,"description":"long intergenic non-protein coding RNA 2315 [Source:HGNC Symbol;Acc:HGNC:53234]"}, {"versioned_ensembl_gene_id":"ENSG00000258385.1","gene_symbol":"AL391516.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41296286,"end":41298734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112984.11","gene_symbol":"KIF20A","gene_name":"kinesin family member 20A [Source:HGNC Symbol;Acc:HGNC:9787]","synonyms":"RAB6KIFL","biotype":"protein_coding","ncbi_id":"10112","summary":null,"start":138178719,"end":138187715,"strand":1,"description":"kinesin family member 20A [Source:HGNC Symbol;Acc:HGNC:9787]"}, {"versioned_ensembl_gene_id":"ENSG00000066136.20","gene_symbol":"NFYC","gene_name":"nuclear transcription factor Y subunit gamma [Source:HGNC Symbol;Acc:HGNC:7806]","synonyms":"CBF-C,NF-YC","biotype":"protein_coding","ncbi_id":"4802","summary":"This gene encodes one subunit of a trimeric complex forming a highly conserved transcription factor that binds with high specificity to CCAAT motifs in the promoters of a variety of genes. The encoded protein, subunit C, forms a tight dimer with the B subunit, a prerequisite for subunit A association. The resulting trimer binds to DNA with high specificity and affinity. Subunits B and C each contain a histone-like motif. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":40691648,"end":40771603,"strand":1,"description":"nuclear transcription factor Y subunit gamma [Source:HGNC Symbol;Acc:HGNC:7806]"}, {"versioned_ensembl_gene_id":"ENSG00000282304.1","gene_symbol":"AC140479.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110245591,"end":110285856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115386.5","gene_symbol":"REG1A","gene_name":"regenerating family member 1 alpha [Source:HGNC Symbol;Acc:HGNC:9951]","synonyms":"PSPS1,PSPS,PSP,REG,PTP","biotype":"protein_coding","ncbi_id":"5967","summary":"This gene is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV, based on the primary structures of the encoded proteins. This gene encodes a protein that is secreted by the exocrine pancreas. It is associated with islet cell regeneration and diabetogenesis and may be involved in pancreatic lithogenesis. Reg family members REG1B, REGL, PAP and this gene are tandemly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication. [provided by RefSeq, Jul 2008]","start":79120362,"end":79123419,"strand":1,"description":"regenerating family member 1 alpha [Source:HGNC Symbol;Acc:HGNC:9951]"}, {"versioned_ensembl_gene_id":"ENSG00000214851.4","gene_symbol":"LINC00612","gene_name":"long intergenic non-protein coding RNA 612 [Source:HGNC Symbol;Acc:HGNC:28621]","synonyms":"MGC40170,FLJ41814,C12orf33","biotype":"processed_transcript","ncbi_id":"253128","summary":null,"start":9055586,"end":9065070,"strand":-1,"description":"long intergenic non-protein coding RNA 612 [Source:HGNC Symbol;Acc:HGNC:28621]"}, {"versioned_ensembl_gene_id":"ENSG00000137270.10","gene_symbol":"GCM1","gene_name":"glial cells missing homolog 1 [Source:HGNC Symbol;Acc:HGNC:4197]","synonyms":"hGCMa,GCMA","biotype":"protein_coding","ncbi_id":"8521","summary":"This gene encodes a DNA-binding protein with a gcm-motif (glial cell missing motif). The encoded protein is a homolog of the Drosophila glial cells missing gene (gcm). This protein binds to the GCM-motif (A/G)CCCGCAT, a novel sequence among known targets of DNA-binding proteins. The N-terminal DNA-binding domain confers the unique DNA-binding activity of this protein. [provided by RefSeq, Jul 2008]","start":53126964,"end":53148829,"strand":-1,"description":"glial cells missing homolog 1 [Source:HGNC Symbol;Acc:HGNC:4197]"}, {"versioned_ensembl_gene_id":"ENSG00000256590.2","gene_symbol":"TRDV3","gene_name":"T-cell receptor delta variable 3 [Source:HGNC Symbol;Acc:HGNC:12264]","synonyms":"hDV103S1","biotype":"TR_V_gene","ncbi_id":"28516","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22469041,"end":22469698,"strand":-1,"description":"T-cell receptor delta variable 3 [Source:HGNC Symbol;Acc:HGNC:12264]"}, {"versioned_ensembl_gene_id":"ENSG00000250144.1","gene_symbol":"AC104619.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135045464,"end":135046850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214807.2","gene_symbol":"NPM1P31","gene_name":"nucleophosmin 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:45210]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287472","summary":null,"start":124867510,"end":124868326,"strand":1,"description":"nucleophosmin 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:45210]"}, {"versioned_ensembl_gene_id":"ENSG00000251002.7","gene_symbol":"AC244502.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22380680,"end":22482959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281501.1","gene_symbol":"AC104662.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25160641,"end":25201440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239739.1","gene_symbol":"AC026316.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170740351,"end":170741365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225955.2","gene_symbol":"CR759770.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573865,"end":29574792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241098.1","gene_symbol":"LINC01994","gene_name":"long intergenic non-protein coding RNA 1994 [Source:HGNC Symbol;Acc:HGNC:52827]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401103","summary":null,"start":182446970,"end":182486364,"strand":-1,"description":"long intergenic non-protein coding RNA 1994 [Source:HGNC Symbol;Acc:HGNC:52827]"}, {"versioned_ensembl_gene_id":"ENSG00000249563.1","gene_symbol":"AC098976.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9733370,"end":9742361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260206.1","gene_symbol":"AC105020.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75636139,"end":75639239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235625.1","gene_symbol":"AL138957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78275720,"end":78277514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152192.7","gene_symbol":"POU4F1","gene_name":"POU class 4 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9218]","synonyms":"RDC-1,BRN3A","biotype":"protein_coding","ncbi_id":"5457","summary":"This gene encodes a member of the POU-IV class of neural transcription factors. This protein is expressed in a subset of retinal ganglion cells and may be involved in the developing sensory nervous system. This protein may also promote the growth of cervical tumors. A translocation of this gene is associated with some adult acute myeloid leukemias. [provided by RefSeq, Mar 2012]","start":78598362,"end":78603560,"strand":-1,"description":"POU class 4 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9218]"}, {"versioned_ensembl_gene_id":"ENSG00000196482.16","gene_symbol":"ESRRG","gene_name":"estrogen related receptor gamma [Source:HGNC Symbol;Acc:HGNC:3474]","synonyms":"NR3B3","biotype":"protein_coding","ncbi_id":"2104","summary":"This gene encodes a member of the estrogen receptor-related receptor (ESRR) family, which belongs to the nuclear hormone receptor superfamily. All members of the ESRR family share an almost identical DNA binding domain, which is composed of two C4-type zinc finger motifs. The ESRR members are orphan nuclear receptors; they bind to the estrogen response element and steroidogenic factor 1 response element, and activate genes controlled by both response elements in the absence of any ligands. The ESRR family is closely related to the estrogen receptor (ER) family. They share target genes, co-regulators and promoters, and by targeting the same set of genes, the ESRRs seem to interfere with the ER-mediated estrogen response in various ways. It has been reported that the family member encoded by this gene functions as a transcriptional activator of DNA cytosine-5-methyltransferases 1 (Dnmt1) expression by direct binding to its response elements in the DNMT1 promoters, modulates cell proliferation and estrogen signaling in breast cancer, and negatively regulates bone morphogenetic protein 2-induced osteoblast differentiation and bone formation. Multiple alternatively spliced transcript variants have been identified, which mainly differ at the 5' end and some of which encode protein isoforms differing in the N-terminal region. [provided by RefSeq, Aug 2011]","start":216503246,"end":217137755,"strand":-1,"description":"estrogen related receptor gamma [Source:HGNC Symbol;Acc:HGNC:3474]"}, {"versioned_ensembl_gene_id":"ENSG00000229865.1","gene_symbol":"RPL31P54","gene_name":"ribosomal protein L31 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36077]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271483","summary":null,"start":78422823,"end":78423192,"strand":1,"description":"ribosomal protein L31 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36077]"}, {"versioned_ensembl_gene_id":"ENSG00000277316.2","gene_symbol":"TAS2R8","gene_name":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]","synonyms":"TRB5,T2R8","biotype":"protein_coding","ncbi_id":"50836","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10806051,"end":10807293,"strand":-1,"description":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]"}, {"versioned_ensembl_gene_id":"ENSG00000262592.2","gene_symbol":"AC068305.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59063055,"end":59063157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204628.11","gene_symbol":"RACK1","gene_name":"receptor for activated C kinase 1 [Source:HGNC Symbol;Acc:HGNC:4399]","synonyms":"H12.3,GNB2L1,Gnb2-rs1","biotype":"protein_coding","ncbi_id":"10399","summary":null,"start":181236909,"end":181248096,"strand":-1,"description":"receptor for activated C kinase 1 [Source:HGNC Symbol;Acc:HGNC:4399]"}, {"versioned_ensembl_gene_id":"ENSG00000227248.1","gene_symbol":"FAM155A-IT1","gene_name":"FAM155A intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41503]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874375","summary":null,"start":107788342,"end":107835451,"strand":-1,"description":"FAM155A intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41503]"}, {"versioned_ensembl_gene_id":"ENSG00000118620.12","gene_symbol":"ZNF430","gene_name":"zinc finger protein 430 [Source:HGNC Symbol;Acc:HGNC:20808]","synonyms":"FLJ13659","biotype":"protein_coding","ncbi_id":"80264","summary":null,"start":21020620,"end":21060050,"strand":1,"description":"zinc finger protein 430 [Source:HGNC Symbol;Acc:HGNC:20808]"}, {"versioned_ensembl_gene_id":"ENSG00000237811.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"dJ271M21.8,PsiGPR53","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537242,"end":29538325,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000268322.1","gene_symbol":"BNIP3P25","gene_name":"BCL2 interacting protein 3 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49705]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421707","summary":null,"start":21318161,"end":21318719,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49705]"}, {"versioned_ensembl_gene_id":"ENSG00000237487.1","gene_symbol":"VN1R48P","gene_name":"vomeronasal 1 receptor 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:37368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312798","summary":null,"start":38504447,"end":38505482,"strand":-1,"description":"vomeronasal 1 receptor 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:37368]"}, {"versioned_ensembl_gene_id":"ENSG00000198502.5","gene_symbol":"HLA-DRB5","gene_name":"major histocompatibility complex, class II, DR beta 5 [Source:HGNC Symbol;Acc:HGNC:4953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3127","summary":"HLA-DRB5 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32517343,"end":32530287,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 5 [Source:HGNC Symbol;Acc:HGNC:4953]"}, {"versioned_ensembl_gene_id":"ENSG00000129675.15","gene_symbol":"ARHGEF6","gene_name":"Rac/Cdc42 guanine nucleotide exchange factor 6 [Source:HGNC Symbol;Acc:HGNC:685]","synonyms":"alphaPIX,alpha-PIX,MRX46,KIAA0006,Cool2,Cool-2","biotype":"protein_coding","ncbi_id":"9459","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein belongs to a family of cytoplasmic proteins that activate the Ras-like family of Rho proteins by exchanging bound GDP for GTP. It may form a complex with G proteins and stimulate Rho-dependent signals. This protein is activated by PI3-kinase. Mutations in this gene can cause X-chromosomal non-specific cognitive disability. [provided by RefSeq, Jul 2008]","start":136665547,"end":136782088,"strand":-1,"description":"Rac/Cdc42 guanine nucleotide exchange factor 6 [Source:HGNC Symbol;Acc:HGNC:685]"}, {"versioned_ensembl_gene_id":"ENSG00000251398.1","gene_symbol":"LINC01256","gene_name":"long intergenic non-protein coding RNA 1256 [Source:HGNC Symbol;Acc:HGNC:49895]","synonyms":"TCONS_l2_00021715","biotype":"lincRNA","ncbi_id":"104355285","summary":null,"start":132591089,"end":132678503,"strand":1,"description":"long intergenic non-protein coding RNA 1256 [Source:HGNC Symbol;Acc:HGNC:49895]"}, {"versioned_ensembl_gene_id":"ENSG00000076685.18","gene_symbol":"NT5C2","gene_name":"5'-nucleotidase, cytosolic II [Source:HGNC Symbol;Acc:HGNC:8022]","synonyms":"SPG65,PNT5,NT5B,GMP,cN-II","biotype":"protein_coding","ncbi_id":"22978","summary":"This gene encodes a hydrolase that serves as an important role in cellular purine metabolism by acting primarily on inosine 5'-monophosphate and other purine nucleotides. [provided by RefSeq, Oct 2011]","start":103088017,"end":103193306,"strand":-1,"description":"5'-nucleotidase, cytosolic II [Source:HGNC Symbol;Acc:HGNC:8022]"}, {"versioned_ensembl_gene_id":"ENSG00000228224.3","gene_symbol":"NACAP1","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24688]","synonyms":"FKSG17","biotype":"transcribed_processed_pseudogene","ncbi_id":"83955","summary":null,"start":101361794,"end":101372707,"strand":1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24688]"}, {"versioned_ensembl_gene_id":"ENSG00000237569.1","gene_symbol":"TUBAP","gene_name":"tubulin alpha pseudogene [Source:HGNC Symbol;Acc:HGNC:12411]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54016","summary":null,"start":23407658,"end":23409128,"strand":-1,"description":"tubulin alpha pseudogene [Source:HGNC Symbol;Acc:HGNC:12411]"}, {"versioned_ensembl_gene_id":"ENSG00000273129.1","gene_symbol":"PACERR","gene_name":"PTGS2 antisense NFKB1 complex-mediated expression regulator RNA [Source:HGNC Symbol;Acc:HGNC:50552]","synonyms":"PTGS2-AS1,PACER","biotype":"lincRNA","ncbi_id":"103752588","summary":"This gene represents transcription of a long non-coding RNA produced in antisense to the prostaglandin-endoperoxide synthase 2 (PTGS2) gene. This transcript interacts with NF-kB transcriptional regulators to promote expression of PTGS2. [provided by RefSeq, Feb 2015]","start":186680622,"end":186681446,"strand":1,"description":"PTGS2 antisense NFKB1 complex-mediated expression regulator RNA [Source:HGNC Symbol;Acc:HGNC:50552]"}, {"versioned_ensembl_gene_id":"ENSG00000144488.14","gene_symbol":"ESPNL","gene_name":"espin like [Source:HGNC Symbol;Acc:HGNC:27937]","synonyms":"FLJ42568","biotype":"protein_coding","ncbi_id":"339768","summary":null,"start":238100157,"end":238133287,"strand":1,"description":"espin like [Source:HGNC Symbol;Acc:HGNC:27937]"}, {"versioned_ensembl_gene_id":"ENSG00000078487.17","gene_symbol":"ZCWPW1","gene_name":"zinc finger CW-type and PWWP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23486]","synonyms":"ZCW1,FLJ10057,DKFZp434N0510","biotype":"protein_coding","ncbi_id":"55063","summary":null,"start":100400826,"end":100428992,"strand":-1,"description":"zinc finger CW-type and PWWP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23486]"}, {"versioned_ensembl_gene_id":"ENSG00000174977.8","gene_symbol":"AC026271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18650195,"end":18651542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261113.1","gene_symbol":"AC009034.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22286708,"end":22288738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234255.8","gene_symbol":"AC012370.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65439888,"end":65456571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260534.1","gene_symbol":"AC100827.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":72589691,"end":72591845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131459.12","gene_symbol":"GFPT2","gene_name":"glutamine-fructose-6-phosphate transaminase 2 [Source:HGNC Symbol;Acc:HGNC:4242]","synonyms":"GFAT2","biotype":"protein_coding","ncbi_id":"9945","summary":null,"start":180300690,"end":180353387,"strand":-1,"description":"glutamine-fructose-6-phosphate transaminase 2 [Source:HGNC Symbol;Acc:HGNC:4242]"}, {"versioned_ensembl_gene_id":"ENSG00000243441.6","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29355241,"end":29431509,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000213900.2","gene_symbol":"AL645927.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489271,"end":29489676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283528.2","gene_symbol":"AC073264.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":143639230,"end":143647646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248101.2","gene_symbol":"AC002116.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":36008638,"end":36014235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244952.2","gene_symbol":"AC123768.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32613733,"end":32615111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282308.1","gene_symbol":"AL121594.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35222174,"end":35222746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258790.1","gene_symbol":"AL121594.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35122549,"end":35317474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077312.8","gene_symbol":"SNRPA","gene_name":"small nuclear ribonucleoprotein polypeptide A [Source:HGNC Symbol;Acc:HGNC:11151]","synonyms":"U1-A,Mud1,U1A","biotype":"protein_coding","ncbi_id":"6626","summary":"The protein encoded by this gene associates with stem loop II of the U1 small nuclear ribonucleoprotein, which binds the 5' splice site of precursor mRNAs and is required for splicing. The encoded protein autoregulates itself by polyadenylation inhibition of its own pre-mRNA via dimerization and has been implicated in the coupling of splicing and polyadenylation. [provided by RefSeq, Oct 2010]","start":40750637,"end":40765389,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide A [Source:HGNC Symbol;Acc:HGNC:11151]"}, {"versioned_ensembl_gene_id":"ENSG00000262678.1","gene_symbol":"AC004771.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4986466,"end":4987324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233760.1","gene_symbol":"AC004947.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26551822,"end":26557200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123739.10","gene_symbol":"PLA2G12A","gene_name":"phospholipase A2 group XIIA [Source:HGNC Symbol;Acc:HGNC:18554]","synonyms":"PLA2G12","biotype":"protein_coding","ncbi_id":"81579","summary":"Secreted phospholipase A2 (sPLA2) enzymes liberate arachidonic acid from phospholipids for production of eicosanoids and exert a variety of physiologic and pathologic effects. Group XII sPLA2s, such as PLA2G12A, have relatively low specific activity and are structurally and functionally distinct from other sPLA2s (Gelb et al., 2000 [PubMed 11031251]).[supplied by OMIM, Mar 2008]","start":109709989,"end":109730077,"strand":-1,"description":"phospholipase A2 group XIIA [Source:HGNC Symbol;Acc:HGNC:18554]"}, {"versioned_ensembl_gene_id":"ENSG00000173166.17","gene_symbol":"RAPH1","gene_name":"Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 [Source:HGNC Symbol;Acc:HGNC:14436]","synonyms":"KIAA1681,ALS2CR9,ALS2CR18","biotype":"protein_coding","ncbi_id":"65059","summary":"This gene encodes a protein that belongs to the Mig10/Rap1-interacting adaptor molecule/Lamellipodin family of adapter proteins, which function in cell migration. Members of this family contain pleckstrin-homology domains, Ras-association domains, and proline-rich C-termini. The protein encoded by this gene regulates actin dynamics through interaction with Ena/Vasodilator proteins as well as direct binding to filamentous actin to regulate actin network assembly. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":203394345,"end":203535410,"strand":-1,"description":"Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 [Source:HGNC Symbol;Acc:HGNC:14436]"}, {"versioned_ensembl_gene_id":"ENSG00000249894.1","gene_symbol":"AC024581.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67800740,"end":67890096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169567.11","gene_symbol":"HINT1","gene_name":"histidine triad nucleotide binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4912]","synonyms":"PRKCNH1,PKCI-1,HINT","biotype":"protein_coding","ncbi_id":"3094","summary":"This gene encodes a protein that hydrolyzes purine nucleotide phosphoramidates substrates, including AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif. This gene is considered a tumor suppressor gene. In addition, mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy. There are several related pseudogenes on chromosome 7. Several transcript variants have been observed. [provided by RefSeq, Dec 2015]","start":131159027,"end":131171735,"strand":-1,"description":"histidine triad nucleotide binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4912]"}, {"versioned_ensembl_gene_id":"ENSG00000162889.10","gene_symbol":"MAPKAPK2","gene_name":"mitogen-activated protein kinase-activated protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:6887]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9261","summary":"This gene encodes a member of the Ser/Thr protein kinase family. This kinase is regulated through direct phosphorylation by p38 MAP kinase. In conjunction with p38 MAP kinase, this kinase is known to be involved in many cellular processes including stress and inflammatory responses, nuclear export, gene expression regulation and cell proliferation. Heat shock protein HSP27 was shown to be one of the substrates of this kinase in vivo. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":206684944,"end":206734283,"strand":1,"description":"mitogen-activated protein kinase-activated protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:6887]"}, {"versioned_ensembl_gene_id":"ENSG00000136939.1","gene_symbol":"OR1L4","gene_name":"olfactory receptor family 1 subfamily L member 4 [Source:HGNC Symbol;Acc:HGNC:8216]","synonyms":"OR9-E,OR1L5","biotype":"protein_coding","ncbi_id":"254973","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122723990,"end":122724925,"strand":1,"description":"olfactory receptor family 1 subfamily L member 4 [Source:HGNC Symbol;Acc:HGNC:8216]"}, {"versioned_ensembl_gene_id":"ENSG00000181036.13","gene_symbol":"FCRL6","gene_name":"Fc receptor like 6 [Source:HGNC Symbol;Acc:HGNC:31910]","synonyms":"IFGP6,FLJ16056,FcRH6","biotype":"protein_coding","ncbi_id":"343413","summary":null,"start":159800511,"end":159816251,"strand":1,"description":"Fc receptor like 6 [Source:HGNC Symbol;Acc:HGNC:31910]"}, {"versioned_ensembl_gene_id":"ENSG00000234125.5","gene_symbol":"EEF1GP8","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44563]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391698","summary":null,"start":129903010,"end":129904163,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44563]"}, {"versioned_ensembl_gene_id":"ENSG00000113269.13","gene_symbol":"RNF130","gene_name":"ring finger protein 130 [Source:HGNC Symbol;Acc:HGNC:18280]","synonyms":"GP,GOLIATH,G1RZFP","biotype":"protein_coding","ncbi_id":"55819","summary":"The protein encoded by this gene contains a RING finger motif and is similar to g1, a Drosophila zinc-finger protein that is expressed in mesoderm and involved in embryonic development. The expression of the mouse counterpart was found to be upregulated in myeloblastic cells following IL3 deprivation, suggesting that this gene may regulate growth factor withdrawal-induced apoptosis of myeloid precursor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":179911651,"end":180072118,"strand":-1,"description":"ring finger protein 130 [Source:HGNC Symbol;Acc:HGNC:18280]"}, {"versioned_ensembl_gene_id":"ENSG00000181514.6","gene_symbol":"FO393414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72598451,"end":72599634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249421.1","gene_symbol":"ADAMTS19-AS1","gene_name":"ADAMTS19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40797]","synonyms":"RP11-346A9.1","biotype":"antisense_RNA","ncbi_id":"103689846","summary":null,"start":129459559,"end":129460689,"strand":-1,"description":"ADAMTS19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40797]"}, {"versioned_ensembl_gene_id":"ENSG00000139364.10","gene_symbol":"TMEM132B","gene_name":"transmembrane protein 132B [Source:HGNC Symbol;Acc:HGNC:29397]","synonyms":"KIAA1906,KIAA1786","biotype":"protein_coding","ncbi_id":"114795","summary":null,"start":125186836,"end":125662377,"strand":1,"description":"transmembrane protein 132B [Source:HGNC Symbol;Acc:HGNC:29397]"}, {"versioned_ensembl_gene_id":"ENSG00000254330.1","gene_symbol":"AC104232.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":64703774,"end":64734459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249489.1","gene_symbol":"GAPDHP70","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:4148]","synonyms":"GAPDL15,GAPDHL15","biotype":"processed_pseudogene","ncbi_id":"642259","summary":null,"start":88408179,"end":88409223,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:4148]"}, {"versioned_ensembl_gene_id":"ENSG00000270885.1","gene_symbol":"RASL10B","gene_name":"RAS like family 10 member B [Source:HGNC Symbol;Acc:HGNC:30295]","synonyms":"VTS58635,RRP17","biotype":"protein_coding","ncbi_id":"91608","summary":null,"start":35731649,"end":35743521,"strand":1,"description":"RAS like family 10 member B [Source:HGNC Symbol;Acc:HGNC:30295]"}, {"versioned_ensembl_gene_id":"ENSG00000196361.9","gene_symbol":"ELAVL3","gene_name":"ELAV like RNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3314]","synonyms":"PLE21,MGC20653,HUCL,HUC,DKFZp547J036","biotype":"protein_coding","ncbi_id":"1995","summary":"A member of the ELAVL protein family, ELAV-like 3 is a neural-specific RNA-binding protein which contains three RNP-type RNA recognition motifs. The observation that ELAVL3 is one of several Hu antigens (neuronal-specific RNA-binding proteins) recognized by the anti-Hu serum antibody present in sera from patients with paraneoplastic encephalomyelitis and sensory neuronopathy (PEM/PSN) suggests it has a role in neurogenesis. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":11451326,"end":11481046,"strand":-1,"description":"ELAV like RNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3314]"}, {"versioned_ensembl_gene_id":"ENSG00000230213.1","gene_symbol":"OR8V1P","gene_name":"olfactory receptor family 8 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:19613]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"282776","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56188379,"end":56189251,"strand":-1,"description":"olfactory receptor family 8 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:19613]"}, {"versioned_ensembl_gene_id":"ENSG00000274601.1","gene_symbol":"AC240442.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135710095,"end":135710377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186654.20","gene_symbol":"PRR5","gene_name":"proline rich 5 [Source:HGNC Symbol;Acc:HGNC:31682]","synonyms":"Protor-1,PP610,FLJ20185k","biotype":"protein_coding","ncbi_id":"55615","summary":"This gene encodes a protein with a proline-rich domain. This gene is located in a region of chromosome 22 reported to contain a tumor suppressor gene that may be involved in breast and colorectal tumorigenesis. The protein is a component of the mammalian target of rapamycin complex 2 (mTORC2), and it regulates platelet-derived growth factor (PDGF) receptor beta expression and PDGF signaling to Akt and S6K1. Alternative splicing and the use of alternative promoters results in transcripts encoding different isoforms. Read-through transcripts from this gene into the downstream Rho GTPase activating protein 8 (ARHGAP8) gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010]","start":44668547,"end":44737681,"strand":1,"description":"proline rich 5 [Source:HGNC Symbol;Acc:HGNC:31682]"}, {"versioned_ensembl_gene_id":"ENSG00000063046.17","gene_symbol":"EIF4B","gene_name":"eukaryotic translation initiation factor 4B [Source:HGNC Symbol;Acc:HGNC:3285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1975","summary":null,"start":53006158,"end":53042209,"strand":1,"description":"eukaryotic translation initiation factor 4B [Source:HGNC Symbol;Acc:HGNC:3285]"}, {"versioned_ensembl_gene_id":"ENSG00000125255.6","gene_symbol":"SLC10A2","gene_name":"solute carrier family 10 member 2 [Source:HGNC Symbol;Acc:HGNC:10906]","synonyms":"ISBT,ASBT","biotype":"protein_coding","ncbi_id":"6555","summary":"This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also critical for cholesterol homeostasis. Mutations in this gene cause primary bile acid malabsorption (PBAM); muatations in this gene may also be associated with other diseases of the liver and intestines, such as familial hypertriglyceridemia (FHTG). [provided by RefSeq, Mar 2010]","start":103043998,"end":103066846,"strand":-1,"description":"solute carrier family 10 member 2 [Source:HGNC Symbol;Acc:HGNC:10906]"}, {"versioned_ensembl_gene_id":"ENSG00000271278.1","gene_symbol":"ELOCP33","gene_name":"elongin C pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49174]","synonyms":"TCEB1P33","biotype":"processed_pseudogene","ncbi_id":"101928827","summary":null,"start":39932454,"end":39933561,"strand":1,"description":"elongin C pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49174]"}, {"versioned_ensembl_gene_id":"ENSG00000258644.5","gene_symbol":"SYNJ2BP-COX16","gene_name":"SYNJ2BP-COX16 readthrough [Source:HGNC Symbol;Acc:HGNC:48350]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529257","summary":"This locus represents naturally occurring read-through transcription between the neighboring SYNJ2BP (synaptojanin 2 binding protein) and COX16 (COX16 cytochrome c oxidase assembly homolog (S. cerevisiae)) genes on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. Alternate splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Feb 2011]","start":70326064,"end":70417074,"strand":-1,"description":"SYNJ2BP-COX16 readthrough [Source:HGNC Symbol;Acc:HGNC:48350]"}, {"versioned_ensembl_gene_id":"ENSG00000204475.9","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31588895,"end":31592985,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000217811.1","gene_symbol":"HNRNPDP2","gene_name":"heterogeneous nuclear ribonucleoprotein D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481661","summary":null,"start":64631205,"end":64631682,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48749]"}, {"versioned_ensembl_gene_id":"ENSG00000259033.1","gene_symbol":"AL356804.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70275296,"end":70291859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152270.8","gene_symbol":"PDE3B","gene_name":"phosphodiesterase 3B [Source:HGNC Symbol;Acc:HGNC:8779]","synonyms":"HcGIP1","biotype":"protein_coding","ncbi_id":"5140","summary":null,"start":14643723,"end":14872044,"strand":1,"description":"phosphodiesterase 3B [Source:HGNC Symbol;Acc:HGNC:8779]"}, {"versioned_ensembl_gene_id":"ENSG00000186281.12","gene_symbol":"GPAT2","gene_name":"glycerol-3-phosphate acyltransferase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:27168]","synonyms":"CT123","biotype":"protein_coding","ncbi_id":"150763","summary":null,"start":96021946,"end":96039451,"strand":-1,"description":"glycerol-3-phosphate acyltransferase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:27168]"}, {"versioned_ensembl_gene_id":"ENSG00000100324.13","gene_symbol":"TAB1","gene_name":"TGF-beta activated kinase 1 (MAP3K7) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:18157]","synonyms":"MAP3K7IP1","biotype":"protein_coding","ncbi_id":"10454","summary":"The protein encoded by this gene was identified as a regulator of the MAP kinase kinase kinase MAP3K7/TAK1, which is known to mediate various intracellular signaling pathways, such as those induced by TGF beta, interleukin 1, and WNT-1. This protein interacts and thus activates TAK1 kinase. It has been shown that the C-terminal portion of this protein is sufficient for binding and activation of TAK1, while a portion of the N-terminus acts as a dominant-negative inhibitor of TGF beta, suggesting that this protein may function as a mediator between TGF beta receptors and TAK1. This protein can also interact with and activate the mitogen-activated protein kinase 14 (MAPK14/p38alpha), and thus represents an alternative activation pathway, in addition to the MAPKK pathways, which contributes to the biological responses of MAPK14 to various stimuli. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":39399741,"end":39437060,"strand":1,"description":"TGF-beta activated kinase 1 (MAP3K7) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:18157]"}, {"versioned_ensembl_gene_id":"ENSG00000130598.15","gene_symbol":"TNNI2","gene_name":"troponin I2, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11946]","synonyms":"DA2B,AMCD2B,FSSV","biotype":"protein_coding","ncbi_id":"7136","summary":"This gene encodes a fast-twitch skeletal muscle protein, a member of the troponin I gene family, and a component of the troponin complex including troponin T, troponin C and troponin I subunits. The troponin complex, along with tropomyosin, is responsible for the calcium-dependent regulation of striated muscle contraction. Mouse studies show that this component is also present in vascular smooth muscle and may play a role in regulation of smooth muscle function. In addition to muscle tissues, this protein is found in corneal epithelium, cartilage where it is an inhibitor of angiogenesis to inhibit tumor growth and metastasis, and mammary gland where it functions as a co-activator of estrogen receptor-related receptor alpha. This protein also suppresses tumor growth in human ovarian carcinoma. Mutations in this gene cause myopathy and distal arthrogryposis type 2B. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]","start":1838989,"end":1841680,"strand":1,"description":"troponin I2, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11946]"}, {"versioned_ensembl_gene_id":"ENSG00000226437.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30371111,"end":30388367,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000105245.9","gene_symbol":"NUMBL","gene_name":"NUMB like, endocytic adaptor protein [Source:HGNC Symbol;Acc:HGNC:8061]","synonyms":"TNRC23,NUMBR,NUMBLIKE,NUMB-R,CTG3a,CAG3A","biotype":"protein_coding","ncbi_id":"9253","summary":null,"start":40665905,"end":40690972,"strand":-1,"description":"NUMB like, endocytic adaptor protein [Source:HGNC Symbol;Acc:HGNC:8061]"}, {"versioned_ensembl_gene_id":"ENSG00000174130.12","gene_symbol":"TLR6","gene_name":"toll like receptor 6 [Source:HGNC Symbol;Acc:HGNC:16711]","synonyms":"CD286","biotype":"protein_coding","ncbi_id":"10333","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This receptor functionally interacts with toll-like receptor 2 to mediate cellular response to bacterial lipoproteins. A Ser249Pro polymorphism in the extracellular domain of the encoded protein may be associated with an increased of asthma is some populations.[provided by RefSeq, Jan 2011]","start":38823715,"end":38856817,"strand":-1,"description":"toll like receptor 6 [Source:HGNC Symbol;Acc:HGNC:16711]"}, {"versioned_ensembl_gene_id":"ENSG00000239618.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLA-92,HLAL,HLA92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30304241,"end":30311591,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000233035.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28986169,"end":28987450,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000228263.8","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"CTL4,NG22,C6orf29,FLJ14491,TPPT","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31845377,"end":31861227,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000231450.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31167475,"end":31171640,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000174428.16","gene_symbol":"GTF2IRD2B","gene_name":"GTF2I repeat domain containing 2B [Source:HGNC Symbol;Acc:HGNC:33125]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389524","summary":"This gene encodes a glycosylated phosphoprotein with a leucine zipper motif, two helix-loop-helix motifs (I repeats) that are similar to domains found in the TFII-I family of transcription factors, one CHARLIE8 transposable element-like sequence, and a BED zinc finger. This gene lies within a region that is deleted in Williams-Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":75092573,"end":75149817,"strand":1,"description":"GTF2I repeat domain containing 2B [Source:HGNC Symbol;Acc:HGNC:33125]"}, {"versioned_ensembl_gene_id":"ENSG00000237247.6","gene_symbol":"MBD3L5","gene_name":"methyl-CpG binding domain protein 3 like 5 [Source:HGNC Symbol;Acc:HGNC:37204]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284428","summary":null,"start":7030578,"end":7033011,"strand":1,"description":"methyl-CpG binding domain protein 3 like 5 [Source:HGNC Symbol;Acc:HGNC:37204]"}, {"versioned_ensembl_gene_id":"ENSG00000233480.1","gene_symbol":"LINC01683","gene_name":"long intergenic non-protein coding RNA 1683 [Source:HGNC Symbol;Acc:HGNC:52471]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372746","summary":null,"start":19893279,"end":19899755,"strand":-1,"description":"long intergenic non-protein coding RNA 1683 [Source:HGNC Symbol;Acc:HGNC:52471]"}, {"versioned_ensembl_gene_id":"ENSG00000181767.3","gene_symbol":"OR8H2","gene_name":"olfactory receptor family 8 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:15308]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390151","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56103687,"end":56107658,"strand":1,"description":"olfactory receptor family 8 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:15308]"}, {"versioned_ensembl_gene_id":"ENSG00000279493.1","gene_symbol":"FP565260.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5011799,"end":5017145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262612.3","gene_symbol":"TAS2R43","gene_name":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]","synonyms":"T2R52","biotype":"protein_coding","ncbi_id":"259289","summary":"TAS2R43 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11091308,"end":11092334,"strand":-1,"description":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]"}, {"versioned_ensembl_gene_id":"ENSG00000233571.1","gene_symbol":"AL592043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34206725,"end":34415537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185448.10","gene_symbol":"FAM47A","gene_name":"family with sequence similarity 47 member A [Source:HGNC Symbol;Acc:HGNC:29962]","synonyms":"MGC27003","biotype":"protein_coding","ncbi_id":"158724","summary":null,"start":34129756,"end":34132314,"strand":-1,"description":"family with sequence similarity 47 member A [Source:HGNC Symbol;Acc:HGNC:29962]"}, {"versioned_ensembl_gene_id":"ENSG00000228560.1","gene_symbol":"AL513323.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159346166,"end":159469068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272803.5","gene_symbol":"PRH2","gene_name":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]","synonyms":"Pr","biotype":"protein_coding","ncbi_id":"5555","summary":"This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. In western population this locus is commonly biallelic and encodes proline-rich protein (PRP) isoforms, PRP-1 and PRP-2. The reference genome encodes the PRP-1 allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Oct 2015]","start":10929236,"end":10932341,"strand":1,"description":"proline rich protein HaeIII subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9367]"}, {"versioned_ensembl_gene_id":"ENSG00000162909.17","gene_symbol":"CAPN2","gene_name":"calpain 2 [Source:HGNC Symbol;Acc:HGNC:1479]","synonyms":"mCANP,CANPml,CANPL2","biotype":"protein_coding","ncbi_id":"824","summary":"The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 2. Multiple heterogeneous transcriptional start sites in the 5' UTR have been reported. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":223701593,"end":223776018,"strand":1,"description":"calpain 2 [Source:HGNC Symbol;Acc:HGNC:1479]"}, {"versioned_ensembl_gene_id":"ENSG00000236678.7","gene_symbol":"LINC00347","gene_name":"long intergenic non-protein coding RNA 347 [Source:HGNC Symbol;Acc:HGNC:27890]","synonyms":null,"biotype":"lincRNA","ncbi_id":"338864","summary":null,"start":74552503,"end":74565445,"strand":1,"description":"long intergenic non-protein coding RNA 347 [Source:HGNC Symbol;Acc:HGNC:27890]"}, {"versioned_ensembl_gene_id":"ENSG00000244088.1","gene_symbol":"RPL23AP44","gene_name":"ribosomal protein L23a pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:35955]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391825","summary":null,"start":121575848,"end":121576320,"strand":-1,"description":"ribosomal protein L23a pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:35955]"}, {"versioned_ensembl_gene_id":"ENSG00000162065.12","gene_symbol":"TBC1D24","gene_name":"TBC1 domain family member 24 [Source:HGNC Symbol;Acc:HGNC:29203]","synonyms":"DFNA65,TLDC6,KIAA1171,DFNB86","biotype":"protein_coding","ncbi_id":"57465","summary":"This gene encodes a protein with a conserved domain, referred to as the TBC domain, characteristic of proteins which interact with GTPases. TBC domain proteins may serve as GTPase-activating proteins for a particular group of GTPases, the Rab (Ras-related proteins in brain) small GTPases which are involved in the regulation of membrane trafficking. Mutations in this gene are associated with familial infantile myoclonic epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2011]","start":2475051,"end":2509560,"strand":1,"description":"TBC1 domain family member 24 [Source:HGNC Symbol;Acc:HGNC:29203]"}, {"versioned_ensembl_gene_id":"ENSG00000177596.1","gene_symbol":"AL355390.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74412957,"end":74419115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257531.2","gene_symbol":"AC008147.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":50217662,"end":50218343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110717.12","gene_symbol":"NDUFS8","gene_name":"NADH:ubiquinone oxidoreductase core subunit S8 [Source:HGNC Symbol;Acc:HGNC:7715]","synonyms":"TYKY,CI-23k","biotype":"protein_coding","ncbi_id":"4728","summary":"This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome. [provided by RefSeq, Mar 2010]","start":68030617,"end":68036644,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S8 [Source:HGNC Symbol;Acc:HGNC:7715]"}, {"versioned_ensembl_gene_id":"ENSG00000151640.12","gene_symbol":"DPYSL4","gene_name":"dihydropyrimidinase like 4 [Source:HGNC Symbol;Acc:HGNC:3016]","synonyms":"ULIP4,DRP-4","biotype":"protein_coding","ncbi_id":"10570","summary":null,"start":132186900,"end":132205776,"strand":1,"description":"dihydropyrimidinase like 4 [Source:HGNC Symbol;Acc:HGNC:3016]"}, {"versioned_ensembl_gene_id":"ENSG00000174501.14","gene_symbol":"ANKRD36C","gene_name":"ankyrin repeat domain 36C [Source:HGNC Symbol;Acc:HGNC:32946]","synonyms":"DKFZp667P0924","biotype":"protein_coding","ncbi_id":"400986","summary":null,"start":95836919,"end":95991831,"strand":-1,"description":"ankyrin repeat domain 36C [Source:HGNC Symbol;Acc:HGNC:32946]"}, {"versioned_ensembl_gene_id":"ENSG00000235278.2","gene_symbol":"ZNF652P1","gene_name":"zinc finger protein 652 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35166]","synonyms":"ZNF652P","biotype":"processed_pseudogene","ncbi_id":"646592","summary":null,"start":50786674,"end":50788285,"strand":-1,"description":"zinc finger protein 652 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35166]"}, {"versioned_ensembl_gene_id":"ENSG00000204403.9","gene_symbol":"CASP12","gene_name":"caspase 12 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19004]","synonyms":"CASP12P1","biotype":"polymorphic_pseudogene","ncbi_id":"100506742","summary":"Caspases are cysteine proteases that cleave C-terminal aspartic acid residues on their substrate molecules. This gene is most highly related to members of the ICE subfamily of caspases that process inflammatory cytokines. In rodents, the homolog of this gene mediates apoptosis in response to endoplasmic reticulum stress. However, in humans this gene contains a polymorphism for the presence or absence of a premature stop codon. The majority of human individuals have the premature stop codon and produce a truncated non-functional protein. The read-through codon occurs primarily in individuals of African descent and carriers have endotoxin hypo-responsiveness and an increased susceptibility to severe sepsis. Several alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Feb 2011]","start":104885718,"end":104898670,"strand":-1,"description":"caspase 12 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19004]"}, {"versioned_ensembl_gene_id":"ENSG00000105379.9","gene_symbol":"ETFB","gene_name":"electron transfer flavoprotein beta subunit [Source:HGNC Symbol;Acc:HGNC:3482]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2109","summary":"This gene encodes electron-transfer-flavoprotein, beta polypeptide, which shuttles electrons between primary flavoprotein dehydrogenases involved in mitochondrial fatty acid and amino acid catabolism and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. The gene deficiencies have been implicated in type II glutaricaciduria. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":51345169,"end":51366418,"strand":-1,"description":"electron transfer flavoprotein beta subunit [Source:HGNC Symbol;Acc:HGNC:3482]"}, {"versioned_ensembl_gene_id":"ENSG00000273988.1","gene_symbol":"AL450472.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135445897,"end":135447368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225769.1","gene_symbol":"CROCCP1","gene_name":"ciliary rootlet coiled-coil, rootletin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33602]","synonyms":"CROCCP","biotype":"processed_pseudogene","ncbi_id":"392547","summary":null,"start":135432960,"end":135438634,"strand":1,"description":"ciliary rootlet coiled-coil, rootletin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33602]"}, {"versioned_ensembl_gene_id":"ENSG00000230980.1","gene_symbol":"RPL36AP39","gene_name":"ribosomal protein L36a pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36074]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271643","summary":null,"start":1792553,"end":1792870,"strand":1,"description":"ribosomal protein L36a pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36074]"}, {"versioned_ensembl_gene_id":"ENSG00000249019.2","gene_symbol":"AC108471.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39713842,"end":39714451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277414.4","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR-8,CD85c,LIR8","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54250781,"end":54257977,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000274373.1","gene_symbol":"AC148476.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132424504,"end":132425208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125633.10","gene_symbol":"CCDC93","gene_name":"coiled-coil domain containing 93 [Source:HGNC Symbol;Acc:HGNC:25611]","synonyms":"FLJ10996","biotype":"protein_coding","ncbi_id":"54520","summary":null,"start":117915478,"end":118014133,"strand":-1,"description":"coiled-coil domain containing 93 [Source:HGNC Symbol;Acc:HGNC:25611]"}, {"versioned_ensembl_gene_id":"ENSG00000219027.2","gene_symbol":"RPS3AP2","gene_name":"ribosomal protein S3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14196]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"64725","summary":null,"start":1477830,"end":1478583,"strand":1,"description":"ribosomal protein S3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14196]"}, {"versioned_ensembl_gene_id":"ENSG00000250686.2","gene_symbol":"AL049544.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":61630233,"end":61681049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172123.12","gene_symbol":"SLFN12","gene_name":"schlafen family member 12 [Source:HGNC Symbol;Acc:HGNC:25500]","synonyms":"FLJ10260","biotype":"protein_coding","ncbi_id":"55106","summary":null,"start":35411060,"end":35433283,"strand":-1,"description":"schlafen family member 12 [Source:HGNC Symbol;Acc:HGNC:25500]"}, {"versioned_ensembl_gene_id":"ENSG00000274024.1","gene_symbol":"AL590282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135297046,"end":135298585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227002.2","gene_symbol":"SNRPEP10","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:43575]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874424","summary":null,"start":223644110,"end":223644383,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:43575]"}, {"versioned_ensembl_gene_id":"ENSG00000080802.18","gene_symbol":"CNOT4","gene_name":"CCR4-NOT transcription complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:7880]","synonyms":"NOT4H,NOT4,CLONE243","biotype":"protein_coding","ncbi_id":"4850","summary":"The protein encoded by this gene is a subunit of the CCR4-NOT complex, a global transcriptional regulator. The encoded protein interacts with CNOT1 and has E3 ubiquitin ligase activity. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]","start":135361795,"end":135510127,"strand":-1,"description":"CCR4-NOT transcription complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:7880]"}, {"versioned_ensembl_gene_id":"ENSG00000166454.9","gene_symbol":"ATMIN","gene_name":"ATM interactor [Source:HGNC Symbol;Acc:HGNC:29034]","synonyms":"ZNF822,KIAA0431,ASCIZ","biotype":"protein_coding","ncbi_id":"23300","summary":null,"start":81035847,"end":81047358,"strand":1,"description":"ATM interactor [Source:HGNC Symbol;Acc:HGNC:29034]"}, {"versioned_ensembl_gene_id":"ENSG00000153802.11","gene_symbol":"TMPRSS11D","gene_name":"transmembrane protease, serine 11D [Source:HGNC Symbol;Acc:HGNC:24059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9407","summary":"This gene encodes a trypsin-like serine protease released from the submucosal serous glands onto mucous membrane. It is a type II integral membrane protein and has 29-38% identity in the sequence of the catalytic region with human hepsin, enteropeptidase, acrosin, and mast cell tryptase. The noncatalytic region has little similarity to other known proteins. This protein may play some biological role in the host defense system on the mucous membrane independently of or in cooperation with other substances in airway mucous or bronchial secretions. [provided by RefSeq, Jul 2008]","start":67820876,"end":67884032,"strand":-1,"description":"transmembrane protease, serine 11D [Source:HGNC Symbol;Acc:HGNC:24059]"}, {"versioned_ensembl_gene_id":"ENSG00000266094.7","gene_symbol":"RASSF5","gene_name":"Ras association domain family member 5 [Source:HGNC Symbol;Acc:HGNC:17609]","synonyms":"RAPL,NORE1,Maxp1","biotype":"protein_coding","ncbi_id":"83593","summary":"This gene is a member of the Ras association domain family. It functions as a tumor suppressor, and is inactivated in a variety of cancers. The encoded protein localizes to centrosomes and microtubules, and associates with the GTP-activated forms of Ras, Rap1, and several other Ras-like small GTPases. The protein regulates lymphocyte adhesion and suppresses cell growth in response to activated Rap1 or Ras. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":206507530,"end":206589448,"strand":1,"description":"Ras association domain family member 5 [Source:HGNC Symbol;Acc:HGNC:17609]"}, {"versioned_ensembl_gene_id":"ENSG00000169291.9","gene_symbol":"SHE","gene_name":"Src homology 2 domain containing E [Source:HGNC Symbol;Acc:HGNC:27004]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126669","summary":null,"start":154469772,"end":154502113,"strand":-1,"description":"Src homology 2 domain containing E [Source:HGNC Symbol;Acc:HGNC:27004]"}, {"versioned_ensembl_gene_id":"ENSG00000198092.5","gene_symbol":"TMPRSS11F","gene_name":"transmembrane protease, serine 11F [Source:HGNC Symbol;Acc:HGNC:29994]","synonyms":"FLJ16046","biotype":"protein_coding","ncbi_id":"389208","summary":null,"start":68053198,"end":68129880,"strand":-1,"description":"transmembrane protease, serine 11F [Source:HGNC Symbol;Acc:HGNC:29994]"}, {"versioned_ensembl_gene_id":"ENSG00000196205.8","gene_symbol":"EEF1A1P5","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3200]","synonyms":"EEF1AL3","biotype":"processed_pseudogene","ncbi_id":"158078","summary":null,"start":133019486,"end":133020874,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3200]"}, {"versioned_ensembl_gene_id":"ENSG00000237222.3","gene_symbol":"LINC01968","gene_name":"long intergenic non-protein coding RNA 1968 [Source:HGNC Symbol;Acc:HGNC:52794]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507391","summary":null,"start":194708421,"end":194782168,"strand":1,"description":"long intergenic non-protein coding RNA 1968 [Source:HGNC Symbol;Acc:HGNC:52794]"}, {"versioned_ensembl_gene_id":"ENSG00000090686.15","gene_symbol":"USP48","gene_name":"ubiquitin specific peptidase 48 [Source:HGNC Symbol;Acc:HGNC:18533]","synonyms":"USP31,MGC14879,FLJ23277,FLJ23054,FLJ20103,FLJ11328","biotype":"protein_coding","ncbi_id":"84196","summary":"This gene encodes a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl-terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C-terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":21678298,"end":21783606,"strand":-1,"description":"ubiquitin specific peptidase 48 [Source:HGNC Symbol;Acc:HGNC:18533]"}, {"versioned_ensembl_gene_id":"ENSG00000055950.16","gene_symbol":"MRPL43","gene_name":"mitochondrial ribosomal protein L43 [Source:HGNC Symbol;Acc:HGNC:14517]","synonyms":"bMRP36a","biotype":"protein_coding","ncbi_id":"84545","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. This gene and the gene for a semaphorin class 4 protein (SEMA4G) overlap at map location 10q24.31 and are transcribed in opposite directions. Sequence analysis identified multiple transcript variants encoding at least four different protein isoforms. [provided by RefSeq, Jul 2008]","start":100969458,"end":100987515,"strand":-1,"description":"mitochondrial ribosomal protein L43 [Source:HGNC Symbol;Acc:HGNC:14517]"}, {"versioned_ensembl_gene_id":"ENSG00000100558.8","gene_symbol":"PLEK2","gene_name":"pleckstrin 2 [Source:HGNC Symbol;Acc:HGNC:19238]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26499","summary":"The protein encoded by this gene associates with membrane-bound phosphatidylinositols generated by phosphatidylinositol 3-kinase. The encoded protein then interacts with the actin cytoskeleton to induce cell spreading. In conjunction with complement component 1, q subcomponent, B chain (C1QB), this gene shows an increase in expression in melanoma cells and may serve as an accurate biomarker for the disease. [provided by RefSeq, Dec 2015]","start":67386983,"end":67412200,"strand":-1,"description":"pleckstrin 2 [Source:HGNC Symbol;Acc:HGNC:19238]"}, {"versioned_ensembl_gene_id":"ENSG00000171405.12","gene_symbol":"XAGE5","gene_name":"X antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:30930]","synonyms":"XAGE-5,GAGED5,CT12.5","biotype":"protein_coding","ncbi_id":"170627","summary":"This gene is a member of the XAGE subfamily, which belongs to the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. The protein encoded by this gene shares a sequence similarity with other GAGE/PAGE proteins. Because of the expression pattern and the sequence similarity, this protein also belongs to a family of CT (cancer-testis) antigens. [provided by RefSeq, Jul 2008]","start":52812204,"end":52818301,"strand":1,"description":"X antigen family member 5 [Source:HGNC Symbol;Acc:HGNC:30930]"}, {"versioned_ensembl_gene_id":"ENSG00000181638.17","gene_symbol":"ZFP41","gene_name":"ZFP41 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:26786]","synonyms":"ZNF753,FLJ38705,FLJ00028","biotype":"protein_coding","ncbi_id":"286128","summary":null,"start":143246821,"end":143262705,"strand":1,"description":"ZFP41 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:26786]"}, {"versioned_ensembl_gene_id":"ENSG00000249317.1","gene_symbol":"AC002460.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":148940941,"end":148942378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088205.12","gene_symbol":"DDX18","gene_name":"DEAD-box helicase 18 [Source:HGNC Symbol;Acc:HGNC:2741]","synonyms":"MrDb,Has1","biotype":"protein_coding","ncbi_id":"8886","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, and it is activated by Myc protein. [provided by RefSeq, Jul 2008]","start":117814650,"end":117832379,"strand":1,"description":"DEAD-box helicase 18 [Source:HGNC Symbol;Acc:HGNC:2741]"}, {"versioned_ensembl_gene_id":"ENSG00000198924.7","gene_symbol":"DCLRE1A","gene_name":"DNA cross-link repair 1A [Source:HGNC Symbol;Acc:HGNC:17660]","synonyms":"KIAA0086,hSNM1,SNM1,PSO2","biotype":"protein_coding","ncbi_id":"9937","summary":"This gene encodes a conserved protein that is involved in the repair of DNA interstrand cross-links. DNA cross-links suppress transcription, replication, and DNA segregation. The encoded protein is a regulator of the mitotic cell cycle checkpoint. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":113834725,"end":113854383,"strand":-1,"description":"DNA cross-link repair 1A [Source:HGNC Symbol;Acc:HGNC:17660]"}, {"versioned_ensembl_gene_id":"ENSG00000268581.1","gene_symbol":"SIGLEC18P","gene_name":"sialic acid binding Ig like lectin 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:15491]","synonyms":"SIGLECP1","biotype":"unprocessed_pseudogene","ncbi_id":"114184","summary":null,"start":51119987,"end":51122965,"strand":1,"description":"sialic acid binding Ig like lectin 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:15491]"}, {"versioned_ensembl_gene_id":"ENSG00000276838.4","gene_symbol":"SERPINF2","gene_name":"serpin family F member 2 [Source:HGNC Symbol;Acc:HGNC:9075]","synonyms":"PLI,API,ALPHA-2-PI,AAP,A2AP","biotype":"protein_coding","ncbi_id":"5345","summary":"This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":1741760,"end":1754189,"strand":1,"description":"serpin family F member 2 [Source:HGNC Symbol;Acc:HGNC:9075]"}, {"versioned_ensembl_gene_id":"ENSG00000221817.9","gene_symbol":"PPP3CB-AS1","gene_name":"PPP3CB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50750]","synonyms":"USP54-AS1","biotype":"processed_transcript","ncbi_id":"101929145","summary":null,"start":73495525,"end":73520070,"strand":1,"description":"PPP3CB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50750]"}, {"versioned_ensembl_gene_id":"ENSG00000254850.2","gene_symbol":"AC004923.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67935558,"end":67935926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254610.3","gene_symbol":"AC004923.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67934563,"end":67955802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249948.6","gene_symbol":"GBA3","gene_name":"glucosylceramidase beta 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19069]","synonyms":"KLrP,GLUC","biotype":"polymorphic_pseudogene","ncbi_id":"57733","summary":"The protein encoded by this gene is an enzyme that can hydrolyze several types of glycosides. This gene is a polymorphic pseudogene, with the most common allele being the functional allele that encodes the full-length protein. Some individuals, as represented by the reference genome allele, contain a single nucleotide polymorphism that results in a premature stop codon in the coding region, and therefore this allele is pseudogenic due to the failure to produce a functional full-length protein. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":22692914,"end":22819575,"strand":1,"description":"glucosylceramidase beta 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19069]"}, {"versioned_ensembl_gene_id":"ENSG00000276318.1","gene_symbol":"GTF2IP8","gene_name":"general transcription factor IIi pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51719]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927717","summary":null,"start":14695422,"end":14706597,"strand":1,"description":"general transcription factor IIi pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51719]"}, {"versioned_ensembl_gene_id":"ENSG00000243672.1","gene_symbol":"AC004924.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67925651,"end":67926431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253532.1","gene_symbol":"AC107909.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":99119352,"end":99120581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173327.7","gene_symbol":"MAP3K11","gene_name":"mitogen-activated protein kinase kinase kinase 11 [Source:HGNC Symbol;Acc:HGNC:6850]","synonyms":"SPRK,PTK1,MLK3,MEKK11","biotype":"protein_coding","ncbi_id":"4296","summary":"The protein encoded by this gene is a member of the serine/threonine kinase family. This kinase contains a SH3 domain and a leucine zipper-basic motif. This kinase preferentially activates MAPK8/JNK kinase, and functions as a positive regulator of JNK signaling pathway. This kinase can directly phosphorylate, and activates IkappaB kinase alpha and beta, and is found to be involved in the transcription activity of NF-kappaB mediated by Rho family GTPases and CDC42. [provided by RefSeq, Jul 2008]","start":65597755,"end":65615382,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 11 [Source:HGNC Symbol;Acc:HGNC:6850]"}, {"versioned_ensembl_gene_id":"ENSG00000187534.6","gene_symbol":"PRR13P5","gene_name":"proline rich 13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440525","summary":null,"start":39943239,"end":39943680,"strand":-1,"description":"proline rich 13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50618]"}, {"versioned_ensembl_gene_id":"ENSG00000206433.10","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31576352,"end":31579139,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000236750.1","gene_symbol":"AC009237.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95641634,"end":95641980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235202.1","gene_symbol":"LINC01525","gene_name":"long intergenic non-protein coding RNA 1525 [Source:HGNC Symbol;Acc:HGNC:51264]","synonyms":"lnc-MAN1A2-1","biotype":"lincRNA","ncbi_id":"104355292","summary":null,"start":117295520,"end":117321336,"strand":1,"description":"long intergenic non-protein coding RNA 1525 [Source:HGNC Symbol;Acc:HGNC:51264]"}, {"versioned_ensembl_gene_id":"ENSG00000245317.2","gene_symbol":"AC008393.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179859013,"end":179861283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264570.1","gene_symbol":"AP005058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14629832,"end":14632806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174996.11","gene_symbol":"KLC2","gene_name":"kinesin light chain 2 [Source:HGNC Symbol;Acc:HGNC:20716]","synonyms":"FLJ12387","biotype":"protein_coding","ncbi_id":"64837","summary":"The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]","start":66257294,"end":66267860,"strand":1,"description":"kinesin light chain 2 [Source:HGNC Symbol;Acc:HGNC:20716]"}, {"versioned_ensembl_gene_id":"ENSG00000165699.13","gene_symbol":"TSC1","gene_name":"tuberous sclerosis 1 [Source:HGNC Symbol;Acc:HGNC:12362]","synonyms":"KIAA0243,hamartin,TSC,LAM","biotype":"protein_coding","ncbi_id":"7248","summary":"This gene is a tumor suppressor gene that encodes the growth inhibitory protein hamartin. The encoded protein interacts with and stabilizes the GTPase activating protein tuberin. This hamartin-tuberin complex negatively regulates mammalian target of rapamycin complex 1 (mTORC1) signalling which is a major regulator of anabolic cell growth. This protein also functions as a co-chaperone for Hsp90 that inhibits its ATPase activity. This protein functions as a facilitator of Hsp90-mediated folding of kinase and non-kinase clients, including Tsc2 and thereby preventing their ubiquitination and proteasomal degradation. Mutations in this gene have been associated with tuberous sclerosis. [provided by RefSeq, Apr 2018]","start":132891348,"end":132944633,"strand":-1,"description":"tuberous sclerosis 1 [Source:HGNC Symbol;Acc:HGNC:12362]"}, {"versioned_ensembl_gene_id":"ENSG00000256518.3","gene_symbol":"AP000812.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72158822,"end":72159734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250562.1","gene_symbol":"RPL38P4","gene_name":"ribosomal protein L38 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130963","summary":null,"start":98525061,"end":98525274,"strand":-1,"description":"ribosomal protein L38 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48867]"}, {"versioned_ensembl_gene_id":"ENSG00000110203.8","gene_symbol":"FOLR3","gene_name":"folate receptor 3 [Source:HGNC Symbol;Acc:HGNC:3795]","synonyms":"FR-G","biotype":"protein_coding","ncbi_id":"2352","summary":"This gene encodes a member of the folate receptor (FOLR) family of proteins, which have a high affinity for folic acid and for several reduced folic acid derivatives, and mediate delivery of 5-methyltetrahydrofolate to the interior of cells. Expression of this gene may be elevated in ovarian and primary peritoneal carcinoma. This gene is present in a gene cluster on chromosome 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":72114869,"end":72139892,"strand":1,"description":"folate receptor 3 [Source:HGNC Symbol;Acc:HGNC:3795]"}, {"versioned_ensembl_gene_id":"ENSG00000140044.12","gene_symbol":"JDP2","gene_name":"Jun dimerization protein 2 [Source:HGNC Symbol;Acc:HGNC:17546]","synonyms":"JUNDM2","biotype":"protein_coding","ncbi_id":"122953","summary":null,"start":75427716,"end":75474111,"strand":1,"description":"Jun dimerization protein 2 [Source:HGNC Symbol;Acc:HGNC:17546]"}, {"versioned_ensembl_gene_id":"ENSG00000259319.1","gene_symbol":"AF111167.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75423683,"end":75427741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177191.2","gene_symbol":"B3GNT8","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:24139]","synonyms":"BGALT15,beta3Gn-T8,B3GALT7","biotype":"protein_coding","ncbi_id":"374907","summary":null,"start":41425359,"end":41428730,"strand":-1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:24139]"}, {"versioned_ensembl_gene_id":"ENSG00000260741.1","gene_symbol":"AC099482.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23194878,"end":23213104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272356.1","gene_symbol":"AL080317.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111309203,"end":111313517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206536.1","gene_symbol":"OR5K3","gene_name":"olfactory receptor family 5 subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:31290]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403277","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98390666,"end":98391631,"strand":1,"description":"olfactory receptor family 5 subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:31290]"}, {"versioned_ensembl_gene_id":"ENSG00000231170.5","gene_symbol":"AC002451.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95596682,"end":95613719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277157.1","gene_symbol":"HIST1H4D","gene_name":"histone cluster 1 H4 family member d [Source:HGNC Symbol;Acc:HGNC:4782]","synonyms":"H4FB,H4/b","biotype":"protein_coding","ncbi_id":"8360","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26188765,"end":26189076,"strand":-1,"description":"histone cluster 1 H4 family member d [Source:HGNC Symbol;Acc:HGNC:4782]"}, {"versioned_ensembl_gene_id":"ENSG00000234104.1","gene_symbol":"AL133465.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20970448,"end":20972562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254891.1","gene_symbol":"OR4A9P","gene_name":"olfactory receptor family 4 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15166]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390137","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55388529,"end":55389472,"strand":1,"description":"olfactory receptor family 4 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15166]"}, {"versioned_ensembl_gene_id":"ENSG00000270123.3","gene_symbol":"VTRNA2-1","gene_name":"vault RNA 2-1 [Source:HGNC Symbol;Acc:HGNC:37054]","synonyms":"VTRNA2,nc886,MIRN886,MIR886,hvg-5,hsa-mir-886,CBL-3","biotype":"vaultRNA","ncbi_id":"100126299","summary":"This gene produces an RNA polymerase III transcript that resembles both a component of the ribonucleoprotein vault particle and a pre-microRNA. However, the RNA product does not function as a vault or microRNA; rather, it acts as a direct inhibitor of protein kinase R (also known as eukaryotic translation initiation factor 2-alpha kinase 2, EIF2AK2), and thereby plays an important role in the regulation of cell growth. This gene is located in the vicinity of a differentially methylated region (DMR) and is imprinted and may show allele-specific expression. This gene is also often hypermethylated and repressed in cancers. [provided by RefSeq, Nov 2015]","start":136080471,"end":136080597,"strand":-1,"description":"vault RNA 2-1 [Source:HGNC Symbol;Acc:HGNC:37054]"}, {"versioned_ensembl_gene_id":"ENSG00000234523.1","gene_symbol":"NDUFB1P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37815]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100380272","summary":null,"start":222945725,"end":222945900,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37815]"}, {"versioned_ensembl_gene_id":"ENSG00000278610.1","gene_symbol":"AC093152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222815064,"end":222994906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171055.14","gene_symbol":"FEZ2","gene_name":"fasciculation and elongation protein zeta 2 [Source:HGNC Symbol;Acc:HGNC:3660]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9637","summary":"This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal bundling and elongation within axon bundles. Other orthologs include the rat gene that encodes zygin II, which can bind to synaptotagmin. [provided by RefSeq, Jul 2008]","start":36531805,"end":36646087,"strand":-1,"description":"fasciculation and elongation protein zeta 2 [Source:HGNC Symbol;Acc:HGNC:3660]"}, {"versioned_ensembl_gene_id":"ENSG00000278886.1","gene_symbol":"AC087821.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18864681,"end":18865247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244018.1","gene_symbol":"RPL35P6","gene_name":"ribosomal protein L35 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35520]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271007","summary":null,"start":18774547,"end":18774918,"strand":-1,"description":"ribosomal protein L35 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35520]"}, {"versioned_ensembl_gene_id":"ENSG00000233319.1","gene_symbol":"PPIAP32","gene_name":"peptidylprolyl isomerase A pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927399","summary":null,"start":130131770,"end":130132241,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49531]"}, {"versioned_ensembl_gene_id":"ENSG00000170921.15","gene_symbol":"TANC2","gene_name":"tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 [Source:HGNC Symbol;Acc:HGNC:30212]","synonyms":"ROLSA,rols,KIAA1636,KIAA1148,FLJ11824,FLJ10215,DKFZP564D166","biotype":"protein_coding","ncbi_id":"26115","summary":null,"start":63009556,"end":63427699,"strand":1,"description":"tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 [Source:HGNC Symbol;Acc:HGNC:30212]"}, {"versioned_ensembl_gene_id":"ENSG00000253335.1","gene_symbol":"AC009884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18989279,"end":19000952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254828.1","gene_symbol":"AP005597.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55302290,"end":55305060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187229.3","gene_symbol":"AC100800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18720905,"end":18734405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242583.1","gene_symbol":"AC008040.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170062244,"end":170062951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226956.1","gene_symbol":"AP000432.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17659276,"end":17660384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254663.1","gene_symbol":"OR4A11P","gene_name":"olfactory receptor family 4 subfamily A member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:15148]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390136","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55318560,"end":55319465,"strand":1,"description":"olfactory receptor family 4 subfamily A member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:15148]"}, {"versioned_ensembl_gene_id":"ENSG00000279648.1","gene_symbol":"AP000432.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17705408,"end":17707455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134253.9","gene_symbol":"TRIM45","gene_name":"tripartite motif containing 45 [Source:HGNC Symbol;Acc:HGNC:19018]","synonyms":"RNF99,FLJ13181","biotype":"protein_coding","ncbi_id":"80263","summary":"This gene encodes a member of the tripartite motif family. The encoded protein may function as a transcriptional repressor of the mitogen-activated protein kinase pathway. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2009]","start":117111060,"end":117122587,"strand":-1,"description":"tripartite motif containing 45 [Source:HGNC Symbol;Acc:HGNC:19018]"}, {"versioned_ensembl_gene_id":"ENSG00000167360.5","gene_symbol":"OR51Q1","gene_name":"olfactory receptor family 51 subfamily Q member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14851]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390061","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5422111,"end":5423206,"strand":1,"description":"olfactory receptor family 51 subfamily Q member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14851]"}, {"versioned_ensembl_gene_id":"ENSG00000140403.12","gene_symbol":"DNAJA4","gene_name":"DnaJ heat shock protein family (Hsp40) member A4 [Source:HGNC Symbol;Acc:HGNC:14885]","synonyms":"PRO1472","biotype":"protein_coding","ncbi_id":"55466","summary":null,"start":78264086,"end":78282196,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A4 [Source:HGNC Symbol;Acc:HGNC:14885]"}, {"versioned_ensembl_gene_id":"ENSG00000264853.1","gene_symbol":"AC011933.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75370947,"end":75373736,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224394.1","gene_symbol":"GPC6-AS2","gene_name":"GPC6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39910]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873973","summary":null,"start":93818424,"end":93836144,"strand":-1,"description":"GPC6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39910]"}, {"versioned_ensembl_gene_id":"ENSG00000101057.15","gene_symbol":"MYBL2","gene_name":"MYB proto-oncogene like 2 [Source:HGNC Symbol;Acc:HGNC:7548]","synonyms":"BMYB,B-MYB","biotype":"protein_coding","ncbi_id":"4605","summary":"The protein encoded by this gene, a member of the MYB family of transcription factor genes, is a nuclear protein involved in cell cycle progression. The encoded protein is phosphorylated by cyclin A/cyclin-dependent kinase 2 during the S-phase of the cell cycle and possesses both activator and repressor activities. It has been shown to activate the cell division cycle 2, cyclin D1, and insulin-like growth factor-binding protein 5 genes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":43667019,"end":43716496,"strand":1,"description":"MYB proto-oncogene like 2 [Source:HGNC Symbol;Acc:HGNC:7548]"}, {"versioned_ensembl_gene_id":"ENSG00000256717.1","gene_symbol":"AP002991.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115659658,"end":115843146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233936.1","gene_symbol":"AL390778.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135245696,"end":135252708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255599.1","gene_symbol":"AP000997.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115628065,"end":115629743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108100.17","gene_symbol":"CCNY","gene_name":"cyclin Y [Source:HGNC Symbol;Acc:HGNC:23354]","synonyms":"CFP1,CBCP1,C10orf9","biotype":"protein_coding","ncbi_id":"219771","summary":"Cyclins, such as CCNY, control cell division cycles and regulate cyclin-dependent kinases (e.g., CDC2; MIM 116940) (Li et al., 2009 [PubMed 18060517]).[supplied by OMIM, May 2009]","start":35247025,"end":35572669,"strand":1,"description":"cyclin Y [Source:HGNC Symbol;Acc:HGNC:23354]"}, {"versioned_ensembl_gene_id":"ENSG00000267309.1","gene_symbol":"AC092295.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36489649,"end":36491040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227068.1","gene_symbol":"AL162584.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125567579,"end":125573023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262096.2","gene_symbol":"PCDHB19P","gene_name":"protocadherin beta 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:14549]","synonyms":"PCDH-PSI5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"84054","summary":null,"start":141239923,"end":141243034,"strand":1,"description":"protocadherin beta 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:14549]"}, {"versioned_ensembl_gene_id":"ENSG00000233200.1","gene_symbol":"AL117336.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35219894,"end":35230598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229898.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29708627,"end":29709049,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000255622.3","gene_symbol":"PCDHB17P","gene_name":"protocadherin beta 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:14547]","synonyms":"PCDHB17,PCDH-psi1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54661","summary":null,"start":141155996,"end":141159061,"strand":1,"description":"protocadherin beta 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:14547]"}, {"versioned_ensembl_gene_id":"ENSG00000243286.1","gene_symbol":"AL929561.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28986785,"end":28988521,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090530.9","gene_symbol":"P3H2","gene_name":"prolyl 3-hydroxylase 2 [Source:HGNC Symbol;Acc:HGNC:19317]","synonyms":"MLAT4,LEPREL1,FLJ10718","biotype":"protein_coding","ncbi_id":"55214","summary":"This gene encodes a member of the prolyl 3-hydroxylase subfamily of 2-oxo-glutarate-dependent dioxygenases. These enzymes play a critical role in collagen chain assembly, stability and cross-linking by catalyzing post-translational 3-hydroxylation of proline residues. Mutations in this gene are associated with nonsyndromic severe myopia with cataract and vitreoretinal degeneration, and downregulation of this gene may play a role in breast cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":189956728,"end":190122437,"strand":-1,"description":"prolyl 3-hydroxylase 2 [Source:HGNC Symbol;Acc:HGNC:19317]"}, {"versioned_ensembl_gene_id":"ENSG00000185825.15","gene_symbol":"BCAP31","gene_name":"B-cell receptor associated protein 31 [Source:HGNC Symbol;Acc:HGNC:16695]","synonyms":"DXS1357E,CDM,BAP31,6C6-Ag","biotype":"protein_coding","ncbi_id":"10134","summary":"This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16. [provided by RefSeq, Jan 2012]","start":153700497,"end":153724697,"strand":-1,"description":"B-cell receptor associated protein 31 [Source:HGNC Symbol;Acc:HGNC:16695]"}, {"versioned_ensembl_gene_id":"ENSG00000277334.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335,NKP46","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54892528,"end":54896443,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000221867.8","gene_symbol":"MAGEA3","gene_name":"MAGE family member A3 [Source:HGNC Symbol;Acc:HGNC:6801]","synonyms":"HIP8,CT1.3,MGC14613,MAGE3,HYPD","biotype":"protein_coding","ncbi_id":"4102","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]","start":152698752,"end":152702347,"strand":1,"description":"MAGE family member A3 [Source:HGNC Symbol;Acc:HGNC:6801]"}, {"versioned_ensembl_gene_id":"ENSG00000188624.2","gene_symbol":"IGFL3","gene_name":"IGF like family member 3 [Source:HGNC Symbol;Acc:HGNC:32930]","synonyms":"UNQ483","biotype":"protein_coding","ncbi_id":"388555","summary":"IGFL3 belongs to the insulin-like growth factor (IGF; see MIM 147440) family of signaling molecules that play critical roles in cellular energy metabolism and in growth and development, especially prenatal growth (Emtage et al., 2006 [PubMed 16890402]).[supplied by OMIM, Mar 2008]","start":46120071,"end":46124674,"strand":-1,"description":"IGF like family member 3 [Source:HGNC Symbol;Acc:HGNC:32930]"}, {"versioned_ensembl_gene_id":"ENSG00000164309.14","gene_symbol":"CMYA5","gene_name":"cardiomyopathy associated 5 [Source:HGNC Symbol;Acc:HGNC:14305]","synonyms":"TRIM76,SPRYD2,myospryn,DKFZp451G223,C5orf10","biotype":"protein_coding","ncbi_id":"202333","summary":null,"start":79689877,"end":79800240,"strand":1,"description":"cardiomyopathy associated 5 [Source:HGNC Symbol;Acc:HGNC:14305]"}, {"versioned_ensembl_gene_id":"ENSG00000235141.1","gene_symbol":"COX6CP17","gene_name":"cytochrome c oxidase subunit 6C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480269","summary":null,"start":7295106,"end":7295290,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49369]"}, {"versioned_ensembl_gene_id":"ENSG00000203710.10","gene_symbol":"CR1","gene_name":"complement C3b/C4b receptor 1 (Knops blood group) [Source:HGNC Symbol;Acc:HGNC:2334]","synonyms":"KN,CD35","biotype":"protein_coding","ncbi_id":"1378","summary":"This gene is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1. The genome is polymorphic at this locus with allele-specific splice variants encoding different isoforms, based on the presence/absence of long homologous repeats (LHRs). The gene encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes, leukocytes, glomerular podocytes, and splenic follicular dendritic cells. The Knops blood group system is a system of antigens located on this protein. The protein mediates cellular binding to particles and immune complexes that have activated complement. Decreases in expression of this protein and/or mutations in this gene have been associated with gallbladder carcinomas, mesangiocapillary glomerulonephritis, systemic lupus erythematosus, sarcoidosis and Alzheimer's disease. Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting, conferring protection against severe malaria. [provided by RefSeq, May 2020]","start":207496147,"end":207640647,"strand":1,"description":"complement C3b/C4b receptor 1 (Knops blood group) [Source:HGNC Symbol;Acc:HGNC:2334]"}, {"versioned_ensembl_gene_id":"ENSG00000176182.5","gene_symbol":"MYPOP","gene_name":"Myb related transcription factor, partner of profilin [Source:HGNC Symbol;Acc:HGNC:20178]","synonyms":"P42pop","biotype":"protein_coding","ncbi_id":"339344","summary":null,"start":45890020,"end":45902604,"strand":-1,"description":"Myb related transcription factor, partner of profilin [Source:HGNC Symbol;Acc:HGNC:20178]"}, {"versioned_ensembl_gene_id":"ENSG00000277879.1","gene_symbol":"AL391988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117267116,"end":117268668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085382.11","gene_symbol":"HACE1","gene_name":"HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21033]","synonyms":"KIAA1320","biotype":"protein_coding","ncbi_id":"57531","summary":"This gene encodes a HECT domain and ankyrin repeat-containing ubiquitin ligase. The encoded protein is involved in specific tagging of target proteins, leading to their subcellular localization or proteasomal degradation. The protein is a potential tumor suppressor and is involved in the pathophysiology of several tumors, including Wilm's tumor. [provided by RefSeq, Mar 2016]","start":104728093,"end":104859919,"strand":-1,"description":"HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21033]"}, {"versioned_ensembl_gene_id":"ENSG00000227535.2","gene_symbol":"AL357315.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":104831129,"end":104845820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159224.4","gene_symbol":"GIP","gene_name":"gastric inhibitory polypeptide [Source:HGNC Symbol;Acc:HGNC:4270]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2695","summary":"This gene encodes an incretin hormone and belongs to the glucagon superfamily. The encoded protein is important in maintaining glucose homeostasis as it is a potent stimulator of insulin secretion from pancreatic beta-cells following food ingestion and nutrient absorption. This gene stimulates insulin secretion via its G protein-coupled receptor activation of adenylyl cyclase and other signal transduction pathways. It is a relatively poor inhibitor of gastric acid secretion. [provided by RefSeq, Jul 2008]","start":48958554,"end":48968596,"strand":-1,"description":"gastric inhibitory polypeptide [Source:HGNC Symbol;Acc:HGNC:4270]"}, {"versioned_ensembl_gene_id":"ENSG00000238059.1","gene_symbol":"HSPE1P21","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:49340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480258","summary":null,"start":133510386,"end":133510693,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:49340]"}, {"versioned_ensembl_gene_id":"ENSG00000276291.5","gene_symbol":"FRG1HP","gene_name":"FSHD region gene 1 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51767]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132352","summary":null,"start":40992249,"end":41218410,"strand":1,"description":"FSHD region gene 1 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51767]"}, {"versioned_ensembl_gene_id":"ENSG00000149564.11","gene_symbol":"ESAM","gene_name":"endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:17474]","synonyms":"W117m","biotype":"protein_coding","ncbi_id":"90952","summary":null,"start":124752583,"end":124762290,"strand":-1,"description":"endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:17474]"}, {"versioned_ensembl_gene_id":"ENSG00000167258.13","gene_symbol":"CDK12","gene_name":"cyclin dependent kinase 12 [Source:HGNC Symbol;Acc:HGNC:24224]","synonyms":"CRKRS,CRKR,CRK7,KIAA0904","biotype":"protein_coding","ncbi_id":"51755","summary":null,"start":39461511,"end":39564907,"strand":1,"description":"cyclin dependent kinase 12 [Source:HGNC Symbol;Acc:HGNC:24224]"}, {"versioned_ensembl_gene_id":"ENSG00000182985.17","gene_symbol":"CADM1","gene_name":"cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:5951]","synonyms":"BL2,TSLC1,SYNCAM1,SYNCAM,ST17,RA175,NECL2,Necl-2,IGSF4A,IGSF4","biotype":"protein_coding","ncbi_id":"23705","summary":null,"start":115169218,"end":115504957,"strand":-1,"description":"cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:5951]"}, {"versioned_ensembl_gene_id":"ENSG00000231166.2","gene_symbol":"TUBB4BP6","gene_name":"tubulin beta 4B class IVb pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42336]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996306","summary":null,"start":118763867,"end":118764345,"strand":1,"description":"tubulin beta 4B class IVb pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42336]"}, {"versioned_ensembl_gene_id":"ENSG00000279609.1","gene_symbol":"AL158070.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":105656369,"end":105657989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214695.3","gene_symbol":"NPAP1P2","gene_name":"nuclear pore associated protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45019]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420829","summary":null,"start":79860573,"end":79861806,"strand":1,"description":"nuclear pore associated protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45019]"}, {"versioned_ensembl_gene_id":"ENSG00000261326.2","gene_symbol":"LINC01355","gene_name":"long intergenic non-protein coding RNA 1355 [Source:HGNC Symbol;Acc:HGNC:50584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996511","summary":null,"start":23281309,"end":23286752,"strand":-1,"description":"long intergenic non-protein coding RNA 1355 [Source:HGNC Symbol;Acc:HGNC:50584]"}, {"versioned_ensembl_gene_id":"ENSG00000275269.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54860626,"end":54876850,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000110013.12","gene_symbol":"SIAE","gene_name":"sialic acid acetylesterase [Source:HGNC Symbol;Acc:HGNC:18187]","synonyms":"YSG2,MGC87009,LSE,CSE-C","biotype":"protein_coding","ncbi_id":"54414","summary":"This gene encodes an enzyme which removes 9-O-acetylation modifications from sialic acids. Mutations in this gene are associated with susceptibility to autoimmune disease 6. Multiple transcript variants encoding different isoforms, found either in the cytosol or in the lysosome, have been found for this gene.[provided by RefSeq, Feb 2011]","start":124633113,"end":124695707,"strand":-1,"description":"sialic acid acetylesterase [Source:HGNC Symbol;Acc:HGNC:18187]"}, {"versioned_ensembl_gene_id":"ENSG00000172638.12","gene_symbol":"EFEMP2","gene_name":"EGF containing fibulin like extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:3219]","synonyms":"UPH1,FBLN4","biotype":"protein_coding","ncbi_id":"30008","summary":"A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jan 2011]","start":65866441,"end":65873592,"strand":-1,"description":"EGF containing fibulin like extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:3219]"}, {"versioned_ensembl_gene_id":"ENSG00000279392.1","gene_symbol":"AL158801.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55229217,"end":55229681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253687.1","gene_symbol":"AC008456.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160613873,"end":160639183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274714.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819131,"end":54834528,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000106327.12","gene_symbol":"TFR2","gene_name":"transferrin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11762]","synonyms":"TFRC2,HFE3","biotype":"protein_coding","ncbi_id":"7036","summary":"This gene encodes a single-pass type II membrane protein, which is a member of the transferrin receptor-like family. This protein mediates cellular uptake of transferrin-bound iron, and may be involved in iron metabolism, hepatocyte function and erythrocyte differentiation. Mutations in this gene have been associated with hereditary hemochromatosis type III. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]","start":100620416,"end":100642779,"strand":-1,"description":"transferrin receptor 2 [Source:HGNC Symbol;Acc:HGNC:11762]"}, {"versioned_ensembl_gene_id":"ENSG00000275601.1","gene_symbol":"AC011330.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43642389,"end":43643023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270811.1","gene_symbol":"AL590095.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7154120,"end":7154236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223581.1","gene_symbol":"AL590095.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7097152,"end":7097675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142046.14","gene_symbol":"TMEM91","gene_name":"transmembrane protein 91 [Source:HGNC Symbol;Acc:HGNC:32393]","synonyms":"IFITMD6,FLJ27310","biotype":"protein_coding","ncbi_id":"641649","summary":null,"start":41350911,"end":41384083,"strand":1,"description":"transmembrane protein 91 [Source:HGNC Symbol;Acc:HGNC:32393]"}, {"versioned_ensembl_gene_id":"ENSG00000260641.1","gene_symbol":"AC114811.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98658904,"end":98664550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152457.17","gene_symbol":"DCLRE1C","gene_name":"DNA cross-link repair 1C [Source:HGNC Symbol;Acc:HGNC:17642]","synonyms":"SCIDA,FLJ11360,ARTEMIS,A-SCID,SNM1C","biotype":"protein_coding","ncbi_id":"64421","summary":"This gene encodes a nuclear protein that is involved in V(D)J recombination and DNA repair. The encoded protein has single-strand-specific 5'-3' exonuclease activity; it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins. The protein also functions in the regulation of the cell cycle in response to DNA damage. Mutations in this gene can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":14897359,"end":14954432,"strand":-1,"description":"DNA cross-link repair 1C [Source:HGNC Symbol;Acc:HGNC:17642]"}, {"versioned_ensembl_gene_id":"ENSG00000188554.13","gene_symbol":"NBR1","gene_name":"NBR1, autophagy cargo receptor [Source:HGNC Symbol;Acc:HGNC:6746]","synonyms":"M17S2,KIAA0049,CA125,1A1-3B","biotype":"protein_coding","ncbi_id":"4077","summary":"The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled-coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of chromosome 17q21.1 that is in close proximity to the BRCA1 tumor suppressor gene. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":43170481,"end":43211689,"strand":1,"description":"NBR1, autophagy cargo receptor [Source:HGNC Symbol;Acc:HGNC:6746]"}, {"versioned_ensembl_gene_id":"ENSG00000255510.1","gene_symbol":"OR8A2P","gene_name":"olfactory receptor family 8 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15306]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390273","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124460534,"end":124461485,"strand":1,"description":"olfactory receptor family 8 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15306]"}, {"versioned_ensembl_gene_id":"ENSG00000251210.5","gene_symbol":"LINC02270","gene_name":"long intergenic non-protein coding RNA 2270 [Source:HGNC Symbol;Acc:HGNC:53185]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929019","summary":null,"start":12223451,"end":12251286,"strand":1,"description":"long intergenic non-protein coding RNA 2270 [Source:HGNC Symbol;Acc:HGNC:53185]"}, {"versioned_ensembl_gene_id":"ENSG00000255048.1","gene_symbol":"OR8X1P","gene_name":"olfactory receptor family 8 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31318]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403305","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124404234,"end":124405102,"strand":-1,"description":"olfactory receptor family 8 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31318]"}, {"versioned_ensembl_gene_id":"ENSG00000284609.1","gene_symbol":"OR8B3","gene_name":"olfactory receptor family 8 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8472]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390271","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124395534,"end":124399024,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8472]"}, {"versioned_ensembl_gene_id":"ENSG00000243643.1","gene_symbol":"TSPY20P","gene_name":"testis specific protein, Y-linked 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:38093]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130848","summary":null,"start":10036195,"end":10038375,"strand":1,"description":"testis specific protein, Y-linked 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:38093]"}, {"versioned_ensembl_gene_id":"ENSG00000284680.1","gene_symbol":"OR8B2","gene_name":"olfactory receptor family 8 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:8471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26595","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124382394,"end":124384462,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:8471]"}, {"versioned_ensembl_gene_id":"ENSG00000175455.14","gene_symbol":"CCDC14","gene_name":"coiled-coil domain containing 14 [Source:HGNC Symbol;Acc:HGNC:25766]","synonyms":"FLJ12892,DKFZp434L1050","biotype":"protein_coding","ncbi_id":"64770","summary":null,"start":123897305,"end":123961408,"strand":-1,"description":"coiled-coil domain containing 14 [Source:HGNC Symbol;Acc:HGNC:25766]"}, {"versioned_ensembl_gene_id":"ENSG00000255225.1","gene_symbol":"AP001804.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":124338783,"end":124339662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105341.18","gene_symbol":"DMAC2","gene_name":"distal membrane arm assembly complex 2 [Source:HGNC Symbol;Acc:HGNC:25496]","synonyms":"FLJ10241,ATP5SL","biotype":"protein_coding","ncbi_id":"55101","summary":null,"start":41431318,"end":41440717,"strand":-1,"description":"distal membrane arm assembly complex 2 [Source:HGNC Symbol;Acc:HGNC:25496]"}, {"versioned_ensembl_gene_id":"ENSG00000257264.5","gene_symbol":"AC136443.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14901499,"end":14902174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184709.7","gene_symbol":"LRRC26","gene_name":"leucine rich repeat containing 26 [Source:HGNC Symbol;Acc:HGNC:31409]","synonyms":"OTTHUMG00000020980,bA350O14.10","biotype":"protein_coding","ncbi_id":"389816","summary":null,"start":137168758,"end":137170051,"strand":-1,"description":"leucine rich repeat containing 26 [Source:HGNC Symbol;Acc:HGNC:31409]"}, {"versioned_ensembl_gene_id":"ENSG00000232294.5","gene_symbol":"AL031674.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52671917,"end":52690929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228074.1","gene_symbol":"UBBP5","gene_name":"ubiquitin B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42645]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873783","summary":null,"start":87219004,"end":87219269,"strand":1,"description":"ubiquitin B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42645]"}, {"versioned_ensembl_gene_id":"ENSG00000197647.11","gene_symbol":"ZNF433","gene_name":"zinc finger protein 433 [Source:HGNC Symbol;Acc:HGNC:20811]","synonyms":"FLJ40981","biotype":"protein_coding","ncbi_id":"163059","summary":null,"start":12014732,"end":12035741,"strand":-1,"description":"zinc finger protein 433 [Source:HGNC Symbol;Acc:HGNC:20811]"}, {"versioned_ensembl_gene_id":"ENSG00000282415.1","gene_symbol":"AC229888.7","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142639852,"end":142640305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237369.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29465074,"end":29470282,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000185432.11","gene_symbol":"METTL7A","gene_name":"methyltransferase like 7A [Source:HGNC Symbol;Acc:HGNC:24550]","synonyms":"DKFZP586A0522","biotype":"protein_coding","ncbi_id":"25840","summary":null,"start":50923472,"end":50932517,"strand":1,"description":"methyltransferase like 7A [Source:HGNC Symbol;Acc:HGNC:24550]"}, {"versioned_ensembl_gene_id":"ENSG00000274370.1","gene_symbol":"AC130371.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83098377,"end":83098987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253949.1","gene_symbol":"AC022634.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108581062,"end":108626767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164841.4","gene_symbol":"TMEM74","gene_name":"transmembrane protein 74 [Source:HGNC Symbol;Acc:HGNC:26409]","synonyms":"NET36,FLJ30668","biotype":"protein_coding","ncbi_id":"157753","summary":null,"start":108606850,"end":108787615,"strand":-1,"description":"transmembrane protein 74 [Source:HGNC Symbol;Acc:HGNC:26409]"}, {"versioned_ensembl_gene_id":"ENSG00000117408.10","gene_symbol":"IPO13","gene_name":"importin 13 [Source:HGNC Symbol;Acc:HGNC:16853]","synonyms":"RANBP13,KIAA0724,IMP13","biotype":"protein_coding","ncbi_id":"9670","summary":"This gene encodes a member of the importin-beta family of nuclear transport proteins. The encoded protein mediates the import of specific cargo proteins from the cytoplasm to the nucleus and is dependent on the Ras-related nuclear protein-GTPase system. The encoded protein is also involved in nuclear export of the eukaryotic translation initiation factor 1A.[provided by RefSeq, Mar 2009]","start":43946939,"end":43968022,"strand":1,"description":"importin 13 [Source:HGNC Symbol;Acc:HGNC:16853]"}, {"versioned_ensembl_gene_id":"ENSG00000213122.4","gene_symbol":"RPL23AP46","gene_name":"ribosomal protein L23a pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:35894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442260","summary":null,"start":132997551,"end":132998040,"strand":-1,"description":"ribosomal protein L23a pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:35894]"}, {"versioned_ensembl_gene_id":"ENSG00000258783.1","gene_symbol":"KRT18P6","gene_name":"keratin 18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:20280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122592","summary":null,"start":35511825,"end":35513089,"strand":-1,"description":"keratin 18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:20280]"}, {"versioned_ensembl_gene_id":"ENSG00000236571.1","gene_symbol":"AC245102.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53337783,"end":53337973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226299.2","gene_symbol":"RPSAP62","gene_name":"ribosomal protein SA pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:35583]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131469","summary":null,"start":53322990,"end":53323822,"strand":1,"description":"ribosomal protein SA pseudogene 62 [Source:HGNC Symbol;Acc:HGNC:35583]"}, {"versioned_ensembl_gene_id":"ENSG00000263477.1","gene_symbol":"AC104982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29863402,"end":29866092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274758.1","gene_symbol":"AC006435.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2366589,"end":2366791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278953.1","gene_symbol":"AP003499.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93592187,"end":93592669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272762.5","gene_symbol":"AC115284.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":51961212,"end":51974031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258597.3","gene_symbol":"SERPINA2","gene_name":"serpin family A member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8985]","synonyms":"SERPINA2P,PIL,ATR,ARGS","biotype":"polymorphic_pseudogene","ncbi_id":"390502","summary":"This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. The encoded intracellular glycoprotein is localized at the endoplasmic reticulum. This gene is a polymorphic pseudogene, with the non-functional allele being predominant in some populations. Some individuals, as represented by the reference genome allele, contain a 2kb coding region deletion and a start code mutation. [provided by RefSeq, Feb 2014]","start":94364313,"end":94366698,"strand":-1,"description":"serpin family A member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8985]"}, {"versioned_ensembl_gene_id":"ENSG00000240240.8","gene_symbol":"BX664727.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":40264971,"end":40329221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198090.3","gene_symbol":"KRTAP4-6","gene_name":"keratin associated protein 4-6 [Source:HGNC Symbol;Acc:HGNC:18909]","synonyms":"KRTAP4-15,KAP4.6,KAP4.15","biotype":"protein_coding","ncbi_id":"81871","summary":null,"start":41139433,"end":41140487,"strand":-1,"description":"keratin associated protein 4-6 [Source:HGNC Symbol;Acc:HGNC:18909]"}, {"versioned_ensembl_gene_id":"ENSG00000234812.1","gene_symbol":"BX664727.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40291275,"end":40291502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273693.1","gene_symbol":"C2orf27AP1","gene_name":"chromosome 2 open reading frame 27A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38413]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420811","summary":null,"start":11085476,"end":11086061,"strand":-1,"description":"chromosome 2 open reading frame 27A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38413]"}, {"versioned_ensembl_gene_id":"ENSG00000205015.1","gene_symbol":"LINC02138","gene_name":"long intergenic non-protein coding RNA 2138 [Source:HGNC Symbol;Acc:HGNC:52998]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400558","summary":null,"start":89166383,"end":89169147,"strand":1,"description":"long intergenic non-protein coding RNA 2138 [Source:HGNC Symbol;Acc:HGNC:52998]"}, {"versioned_ensembl_gene_id":"ENSG00000226370.1","gene_symbol":"LINC00375","gene_name":"long intergenic non-protein coding RNA 375 [Source:HGNC Symbol;Acc:HGNC:42699]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355140","summary":null,"start":85065087,"end":85078920,"strand":-1,"description":"long intergenic non-protein coding RNA 375 [Source:HGNC Symbol;Acc:HGNC:42699]"}, {"versioned_ensembl_gene_id":"ENSG00000198208.11","gene_symbol":"RPS6KL1","gene_name":"ribosomal protein S6 kinase like 1 [Source:HGNC Symbol;Acc:HGNC:20222]","synonyms":"MGC11287","biotype":"protein_coding","ncbi_id":"83694","summary":null,"start":74903954,"end":74923396,"strand":-1,"description":"ribosomal protein S6 kinase like 1 [Source:HGNC Symbol;Acc:HGNC:20222]"}, {"versioned_ensembl_gene_id":"ENSG00000106410.14","gene_symbol":"NOBOX","gene_name":"NOBOX oogenesis homeobox [Source:HGNC Symbol;Acc:HGNC:22448]","synonyms":"Og2x,OG2","biotype":"protein_coding","ncbi_id":"135935","summary":"This homeobox gene encodes a transcription factor that is thought to play a role in oogenesis. In mice, it is essential for folliculogenesis and regulation of oocyte-specific genes. Defects in this gene result in premature ovarian failure type 5.[provided by RefSeq, May 2011]","start":144397240,"end":144410227,"strand":-1,"description":"NOBOX oogenesis homeobox [Source:HGNC Symbol;Acc:HGNC:22448]"}, {"versioned_ensembl_gene_id":"ENSG00000278958.1","gene_symbol":"AC091931.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":104434772,"end":104435499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113013.12","gene_symbol":"HSPA9","gene_name":"heat shock protein family A (Hsp70) member 9 [Source:HGNC Symbol;Acc:HGNC:5244]","synonyms":"mthsp75,mot-2,HSPA9B,GRP75,PBP74","biotype":"protein_coding","ncbi_id":"3313","summary":"This gene encodes a member of the heat shock protein 70 gene family. The encoded protein is primarily localized to the mitochondria but is also found in the endoplasmic reticulum, plasma membrane and cytoplasmic vesicles. This protein is a heat-shock cognate protein. This protein plays a role in cell proliferation, stress response and maintenance of the mitochondria. A pseudogene of this gene is found on chromosome 2.[provided by RefSeq, May 2010]","start":138554882,"end":138575444,"strand":-1,"description":"heat shock protein family A (Hsp70) member 9 [Source:HGNC Symbol;Acc:HGNC:5244]"}, {"versioned_ensembl_gene_id":"ENSG00000283176.1","gene_symbol":"AC103706.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133515506,"end":133515745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065675.14","gene_symbol":"PRKCQ","gene_name":"protein kinase C theta [Source:HGNC Symbol;Acc:HGNC:9410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5588","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role. The protein encoded by this gene is one of the PKC family members. It is a calcium-independent and phospholipid-dependent protein kinase. This kinase is important for T-cell activation. It is required for the activation of the transcription factors NF-kappaB and AP-1, and may link the T cell receptor (TCR) signaling complex to the activation of the transcription factors. [provided by RefSeq, Jul 2008]","start":6427143,"end":6580301,"strand":-1,"description":"protein kinase C theta [Source:HGNC Symbol;Acc:HGNC:9410]"}, {"versioned_ensembl_gene_id":"ENSG00000122484.8","gene_symbol":"RPAP2","gene_name":"RNA polymerase II associated protein 2 [Source:HGNC Symbol;Acc:HGNC:25791]","synonyms":"Rtr1,FLJ13150,C1orf82","biotype":"protein_coding","ncbi_id":"79871","summary":null,"start":92298965,"end":92402056,"strand":1,"description":"RNA polymerase II associated protein 2 [Source:HGNC Symbol;Acc:HGNC:25791]"}, {"versioned_ensembl_gene_id":"ENSG00000198720.12","gene_symbol":"ANKRD13B","gene_name":"ankyrin repeat domain 13B [Source:HGNC Symbol;Acc:HGNC:26363]","synonyms":"FLJ25555","biotype":"protein_coding","ncbi_id":"124930","summary":null,"start":29589769,"end":29614761,"strand":1,"description":"ankyrin repeat domain 13B [Source:HGNC Symbol;Acc:HGNC:26363]"}, {"versioned_ensembl_gene_id":"ENSG00000171291.8","gene_symbol":"ZNF439","gene_name":"zinc finger protein 439 [Source:HGNC Symbol;Acc:HGNC:20873]","synonyms":"DKFZp571K0837","biotype":"protein_coding","ncbi_id":"90594","summary":null,"start":11848726,"end":11883750,"strand":1,"description":"zinc finger protein 439 [Source:HGNC Symbol;Acc:HGNC:20873]"}, {"versioned_ensembl_gene_id":"ENSG00000188739.14","gene_symbol":"RBM34","gene_name":"RNA binding motif protein 34 [Source:HGNC Symbol;Acc:HGNC:28965]","synonyms":"KIAA0117","biotype":"protein_coding","ncbi_id":"23029","summary":"This gene encodes a member of the RNA-binding motif family of RNA recognition motif proteins. The encoded protein contains an RNA-binding domain made up of two RNA recognition motif subdomains referred to as RNA recognition motif-1 and RNA recognition motif-2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":235131183,"end":235161457,"strand":-1,"description":"RNA binding motif protein 34 [Source:HGNC Symbol;Acc:HGNC:28965]"}, {"versioned_ensembl_gene_id":"ENSG00000105568.17","gene_symbol":"PPP2R1A","gene_name":"protein phosphatase 2 scaffold subunit Aalpha [Source:HGNC Symbol;Acc:HGNC:9302]","synonyms":"PR65A,PP2AA,PP2A-Aalpha","biotype":"protein_coding","ncbi_id":"5518","summary":"This gene encodes a constant regulatory subunit of protein phosphatase 2. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The constant regulatory subunit A serves as a scaffolding molecule to coordinate the assembly of the catalytic subunit and a variable regulatory B subunit. This gene encodes an alpha isoform of the constant regulatory subunit A. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":52190039,"end":52229533,"strand":1,"description":"protein phosphatase 2 scaffold subunit Aalpha [Source:HGNC Symbol;Acc:HGNC:9302]"}, {"versioned_ensembl_gene_id":"ENSG00000149273.14","gene_symbol":"RPS3","gene_name":"ribosomal protein S3 [Source:HGNC Symbol;Acc:HGNC:10420]","synonyms":"S3,MGC87870,FLJ27450,FLJ26283","biotype":"protein_coding","ncbi_id":"6188","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit, where it forms part of the domain where translation is initiated. The protein belongs to the S3P family of ribosomal proteins. Studies of the mouse and rat proteins have demonstrated that the protein has an extraribosomal role as an endonuclease involved in the repair of UV-induced DNA damage. The protein appears to be located in both the cytoplasm and nucleus but not in the nucleolus. Higher levels of expression of this gene in colon adenocarcinomas and adenomatous polyps compared to adjacent normal colonic mucosa have been observed. This gene is co-transcribed with the small nucleolar RNA genes U15A and U15B, which are located in its first and fifth introns, respectively. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":75399486,"end":75422280,"strand":1,"description":"ribosomal protein S3 [Source:HGNC Symbol;Acc:HGNC:10420]"}, {"versioned_ensembl_gene_id":"ENSG00000264435.1","gene_symbol":"AC104982.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":29972514,"end":29973027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262251.1","gene_symbol":"AC087388.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7685260,"end":7686371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246731.2","gene_symbol":"MGC16275","gene_name":"uncharacterized protein MGC16275 [Source:NCBI gene;Acc:85001]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"85001","summary":null,"start":74209980,"end":74213342,"strand":-1,"description":"uncharacterized protein MGC16275 [Source:NCBI gene;Acc:85001]"}, {"versioned_ensembl_gene_id":"ENSG00000137575.11","gene_symbol":"SDCBP","gene_name":"syndecan binding protein [Source:HGNC Symbol;Acc:HGNC:10662]","synonyms":"SYCL,MDA-9","biotype":"protein_coding","ncbi_id":"6386","summary":"The protein encoded by this gene was initially identified as a molecule linking syndecan-mediated signaling to the cytoskeleton. The syntenin protein contains tandemly repeated PDZ domains that bind the cytoplasmic, C-terminal domains of a variety of transmembrane proteins. This protein may also affect cytoskeletal-membrane organization, cell adhesion, protein trafficking, and the activation of transcription factors. The protein is primarily localized to membrane-associated adherens junctions and focal adhesions but is also found at the endoplasmic reticulum and nucleus. Alternative splicing results in multiple transcript variants encoding different isoforms. Related pseudogenes have been identified on multiple chromosomes. [provided by RefSeq, Jan 2017]","start":58552924,"end":58582860,"strand":1,"description":"syndecan binding protein [Source:HGNC Symbol;Acc:HGNC:10662]"}, {"versioned_ensembl_gene_id":"ENSG00000224188.1","gene_symbol":"UBE2D3P4","gene_name":"ubiquitin conjugating enzyme E2 D3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39391]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131800","summary":null,"start":84020327,"end":84020762,"strand":1,"description":"ubiquitin conjugating enzyme E2 D3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39391]"}, {"versioned_ensembl_gene_id":"ENSG00000256852.1","gene_symbol":"KNOP1P1","gene_name":"lysine rich nucleolar protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129937","summary":null,"start":24583561,"end":24584549,"strand":1,"description":"lysine rich nucleolar protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48919]"}, {"versioned_ensembl_gene_id":"ENSG00000196781.14","gene_symbol":"TLE1","gene_name":"transducin like enhancer of split 1 [Source:HGNC Symbol;Acc:HGNC:11837]","synonyms":"GRG1,ESG1,ESG","biotype":"protein_coding","ncbi_id":"7088","summary":null,"start":81583683,"end":81689305,"strand":-1,"description":"transducin like enhancer of split 1 [Source:HGNC Symbol;Acc:HGNC:11837]"}, {"versioned_ensembl_gene_id":"ENSG00000253776.1","gene_symbol":"AC099520.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104773641,"end":104799772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141560.14","gene_symbol":"FN3KRP","gene_name":"fructosamine 3 kinase related protein [Source:HGNC Symbol;Acc:HGNC:25700]","synonyms":"FLJ12171,FN3KL","biotype":"protein_coding","ncbi_id":"79672","summary":"A high concentration of glucose can result in non-enzymatic oxidation of proteins by reaction of glucose and lysine residues (glycation). Proteins modified in this way are less active or functional. This gene encodes an enzyme which catalyzes the phosphorylation of psicosamines and ribulosamines compared to the neighboring gene which encodes a highly similar enzyme, fructosamine-3-kinase, which has different substrate specificity. The activity of both enzymes may result in deglycation of proteins to restore their function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":82716683,"end":82730328,"strand":1,"description":"fructosamine 3 kinase related protein [Source:HGNC Symbol;Acc:HGNC:25700]"}, {"versioned_ensembl_gene_id":"ENSG00000253315.1","gene_symbol":"LINC01932","gene_name":"long intergenic non-protein coding RNA 1932 [Source:HGNC Symbol;Acc:HGNC:52755]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377682","summary":null,"start":159227715,"end":159245127,"strand":1,"description":"long intergenic non-protein coding RNA 1932 [Source:HGNC Symbol;Acc:HGNC:52755]"}, {"versioned_ensembl_gene_id":"ENSG00000266357.5","gene_symbol":"LINC02074","gene_name":"long intergenic non-protein coding RNA 2074 [Source:HGNC Symbol;Acc:HGNC:52920]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723567","summary":null,"start":74043452,"end":74154212,"strand":-1,"description":"long intergenic non-protein coding RNA 2074 [Source:HGNC Symbol;Acc:HGNC:52920]"}, {"versioned_ensembl_gene_id":"ENSG00000266765.1","gene_symbol":"AC137735.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73894749,"end":73911878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265927.1","gene_symbol":"AC125421.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73831572,"end":73836019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143093.14","gene_symbol":"STRIP1","gene_name":"striatin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:25916]","synonyms":"KIAA1761,FLJ14743,FAR11A,FAM40A","biotype":"protein_coding","ncbi_id":"85369","summary":"This gene encodes a member of the striatin-interacting phosphatase and kinase complex, which is involved in localization of the Golgi body. The encoded protein participates in cytosketelal organization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":110031577,"end":110074641,"strand":1,"description":"striatin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:25916]"}, {"versioned_ensembl_gene_id":"ENSG00000156150.6","gene_symbol":"ALX3","gene_name":"ALX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:449]","synonyms":"FND","biotype":"protein_coding","ncbi_id":"257","summary":"This gene encodes a nuclear protein with a homeobox DNA-binding domain that functions as a transcriptional regulator involved in cell-type differentiation and development. Preferential methylation of this gene's promoter is associated with advanced-stage neuroblastoma tumors. [provided by RefSeq, Jul 2008]","start":110059994,"end":110070700,"strand":-1,"description":"ALX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:449]"}, {"versioned_ensembl_gene_id":"ENSG00000225259.4","gene_symbol":"ST13P6","gene_name":"ST13, Hsp70 interacting protein pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18557]","synonyms":"FAM10A6P,FAM10A6","biotype":"processed_pseudogene","ncbi_id":"157530","summary":null,"start":133408006,"end":133409107,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18557]"}, {"versioned_ensembl_gene_id":"ENSG00000234736.5","gene_symbol":"FAM170B-AS1","gene_name":"FAM170B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45006]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506733","summary":null,"start":49121839,"end":49151547,"strand":1,"description":"FAM170B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45006]"}, {"versioned_ensembl_gene_id":"ENSG00000273416.1","gene_symbol":"AL732292.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235104180,"end":235104609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233018.1","gene_symbol":"AL732292.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235097187,"end":235097412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253328.2","gene_symbol":"SUMO2P19","gene_name":"SUMO2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49357]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422265","summary":null,"start":102242040,"end":102242619,"strand":-1,"description":"SUMO2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49357]"}, {"versioned_ensembl_gene_id":"ENSG00000272037.1","gene_symbol":"AP002907.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102256392,"end":102257821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260381.2","gene_symbol":"AC007610.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50100339,"end":50121943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115677.16","gene_symbol":"HDLBP","gene_name":"high density lipoprotein binding protein [Source:HGNC Symbol;Acc:HGNC:4857]","synonyms":"VGL,HBP","biotype":"protein_coding","ncbi_id":"3069","summary":"The protein encoded by this gene binds high density lipoprotein (HDL) and may function to regulate excess cholesterol levels in cells. The encoded protein also binds RNA and can induce heterochromatin formation. [provided by RefSeq, Mar 2016]","start":241227264,"end":241317061,"strand":-1,"description":"high density lipoprotein binding protein [Source:HGNC Symbol;Acc:HGNC:4857]"}, {"versioned_ensembl_gene_id":"ENSG00000242899.1","gene_symbol":"RPL7P16","gene_name":"ribosomal protein L7 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36591]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729677","summary":null,"start":132243528,"end":132244265,"strand":-1,"description":"ribosomal protein L7 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36591]"}, {"versioned_ensembl_gene_id":"ENSG00000240854.1","gene_symbol":"AC117409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132175402,"end":132176711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264196.1","gene_symbol":"AC011120.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72839039,"end":72839718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250734.2","gene_symbol":"AL391335.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151612038,"end":151613363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250295.6","gene_symbol":"RDH10-AS1","gene_name":"RDH10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51658]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926926","summary":null,"start":73297711,"end":73356461,"strand":-1,"description":"RDH10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51658]"}, {"versioned_ensembl_gene_id":"ENSG00000263893.2","gene_symbol":"AC080037.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72642731,"end":72644490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234115.2","gene_symbol":"AL138878.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7516600,"end":7517840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230089.1","gene_symbol":"BX248084.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29224848,"end":29267951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219993.1","gene_symbol":"AL138878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7506203,"end":7506549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000056678.11","gene_symbol":"KIFC1","gene_name":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]","synonyms":"KNSL2,HSET","biotype":"processed_transcript","ncbi_id":"3833","summary":null,"start":33561891,"end":33562220,"strand":1,"description":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]"}, {"versioned_ensembl_gene_id":"ENSG00000243514.2","gene_symbol":"RPL32P33","gene_name":"ribosomal protein L32 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36231]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271493","summary":null,"start":72627231,"end":72627624,"strand":1,"description":"ribosomal protein L32 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36231]"}, {"versioned_ensembl_gene_id":"ENSG00000227726.1","gene_symbol":"AP001271.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70477277,"end":70477592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162105.17","gene_symbol":"SHANK2","gene_name":"SH3 and multiple ankyrin repeat domains 2 [Source:HGNC Symbol;Acc:HGNC:14295]","synonyms":"SHANK,ProSAP1,CTTNBP1,CORTBP1,SPANK-3","biotype":"protein_coding","ncbi_id":"22941","summary":"This gene encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein-protein interaction, including ankyrin repeats, and an SH3 domain. This particular family member contains a PDZ domain, a consensus sequence for cortactin SH3 domain-binding peptides and a sterile alpha motif. The alternative splicing demonstrated in Shank genes has been suggested as a mechanism for regulating the molecular structure of Shank and the spectrum of Shank-interacting proteins in the postsynaptic densities of the adult and developing brain. Alterations in the encoded protein may be associated with susceptibility to autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":70467856,"end":71252577,"strand":-1,"description":"SH3 and multiple ankyrin repeat domains 2 [Source:HGNC Symbol;Acc:HGNC:14295]"}, {"versioned_ensembl_gene_id":"ENSG00000228118.3","gene_symbol":"MYL6P5","gene_name":"myosin light chain 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"124685","summary":null,"start":71620978,"end":71621436,"strand":1,"description":"myosin light chain 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51646]"}, {"versioned_ensembl_gene_id":"ENSG00000267603.1","gene_symbol":"LINC01028","gene_name":"long intergenic non-protein coding RNA 1028 [Source:HGNC Symbol;Acc:HGNC:49014]","synonyms":"TCONS_00025127","biotype":"lincRNA","ncbi_id":"101928141","summary":null,"start":70051277,"end":70068095,"strand":1,"description":"long intergenic non-protein coding RNA 1028 [Source:HGNC Symbol;Acc:HGNC:49014]"}, {"versioned_ensembl_gene_id":"ENSG00000251574.6","gene_symbol":"AC099520.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104383298,"end":105392970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270241.1","gene_symbol":"AC115286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34276859,"end":34277292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279860.1","gene_symbol":"AC008568.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":121363002,"end":121365314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258587.1","gene_symbol":"AC006530.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74873684,"end":74874254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230979.3","gene_symbol":"AC079250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47690716,"end":47691246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271569.1","gene_symbol":"IGKV1OR2-6","gene_name":"immunoglobulin kappa variable 1/OR2-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5770]","synonyms":"IGKV1/OR2-6","biotype":"IG_V_pseudogene","ncbi_id":"28865","summary":null,"start":97355059,"end":97355335,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5770]"}, {"versioned_ensembl_gene_id":"ENSG00000268458.1","gene_symbol":"AC011468.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52142626,"end":52144156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280927.1","gene_symbol":"CTBP1-AS","gene_name":"CTBP1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:48337]","synonyms":"PCAT10","biotype":"antisense_RNA","ncbi_id":"285463","summary":null,"start":1210120,"end":1218591,"strand":1,"description":"CTBP1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:48337]"}, {"versioned_ensembl_gene_id":"ENSG00000232418.1","gene_symbol":"AC074348.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53787167,"end":53787298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196273.7","gene_symbol":"LINC00523","gene_name":"long intergenic non-protein coding RNA 523 [Source:HGNC Symbol;Acc:HGNC:20117]","synonyms":"C14orf70","biotype":"lincRNA","ncbi_id":"283601","summary":null,"start":100657250,"end":100676069,"strand":1,"description":"long intergenic non-protein coding RNA 523 [Source:HGNC Symbol;Acc:HGNC:20117]"}, {"versioned_ensembl_gene_id":"ENSG00000244578.1","gene_symbol":"LINC01391","gene_name":"long intergenic non-protein coding RNA 1391 [Source:HGNC Symbol;Acc:HGNC:50666]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103344930","summary":null,"start":138935189,"end":138944020,"strand":-1,"description":"long intergenic non-protein coding RNA 1391 [Source:HGNC Symbol;Acc:HGNC:50666]"}, {"versioned_ensembl_gene_id":"ENSG00000268051.1","gene_symbol":"AC008395.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37963853,"end":37964790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188199.10","gene_symbol":"NUTM2B","gene_name":"NUT family member 2B [Source:HGNC Symbol;Acc:HGNC:23445]","synonyms":"FAM22B,bA119F19.1","biotype":"protein_coding","ncbi_id":"729262","summary":null,"start":79703227,"end":79714681,"strand":1,"description":"NUT family member 2B [Source:HGNC Symbol;Acc:HGNC:23445]"}, {"versioned_ensembl_gene_id":"ENSG00000151948.11","gene_symbol":"GLT1D1","gene_name":"glycosyltransferase 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26483]","synonyms":"FLJ31978","biotype":"protein_coding","ncbi_id":"144423","summary":null,"start":128853427,"end":128984968,"strand":1,"description":"glycosyltransferase 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26483]"}, {"versioned_ensembl_gene_id":"ENSG00000259703.5","gene_symbol":"LINC00593","gene_name":"long intergenic non-protein coding RNA 593 [Source:HGNC Symbol;Acc:HGNC:32382]","synonyms":"C15orf50,MGC42951","biotype":"lincRNA","ncbi_id":"414926","summary":null,"start":69835234,"end":69843120,"strand":1,"description":"long intergenic non-protein coding RNA 593 [Source:HGNC Symbol;Acc:HGNC:32382]"}, {"versioned_ensembl_gene_id":"ENSG00000231547.1","gene_symbol":"AC096632.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":202999738,"end":203000352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231663.1","gene_symbol":"AL355472.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234372807,"end":234373593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236358.1","gene_symbol":"AL355472.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234357006,"end":234365828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237453.1","gene_symbol":"AC096536.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54792885,"end":54794905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271544.1","gene_symbol":"AC006499.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10238213,"end":10238235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132109.9","gene_symbol":"TRIM21","gene_name":"tripartite motif containing 21 [Source:HGNC Symbol;Acc:HGNC:11312]","synonyms":"Ro/SSA,RNF81,SSA1,RO52","biotype":"protein_coding","ncbi_id":"6737","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The encoded protein is part of the RoSSA ribonucleoprotein, which includes a single polypeptide and one of four small RNA molecules. The RoSSA particle localizes to both the cytoplasm and the nucleus. RoSSA interacts with autoantigens in patients with Sjogren syndrome and systemic lupus erythematosus. Alternatively spliced transcript variants for this gene have been described but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]","start":4384897,"end":4393696,"strand":-1,"description":"tripartite motif containing 21 [Source:HGNC Symbol;Acc:HGNC:11312]"}, {"versioned_ensembl_gene_id":"ENSG00000257449.1","gene_symbol":"AC034102.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56029649,"end":56041806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171295.12","gene_symbol":"ZNF440","gene_name":"zinc finger protein 440 [Source:HGNC Symbol;Acc:HGNC:20874]","synonyms":"FLJ37933","biotype":"protein_coding","ncbi_id":"126070","summary":null,"start":11814284,"end":11835201,"strand":1,"description":"zinc finger protein 440 [Source:HGNC Symbol;Acc:HGNC:20874]"}, {"versioned_ensembl_gene_id":"ENSG00000119596.17","gene_symbol":"YLPM1","gene_name":"YLP motif containing 1 [Source:HGNC Symbol;Acc:HGNC:17798]","synonyms":"ZAP,PPP1R169,C14orf170","biotype":"protein_coding","ncbi_id":"56252","summary":null,"start":74763366,"end":74859435,"strand":1,"description":"YLP motif containing 1 [Source:HGNC Symbol;Acc:HGNC:17798]"}, {"versioned_ensembl_gene_id":"ENSG00000178082.6","gene_symbol":"AC005412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29203426,"end":29204474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227858.1","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672598,"end":29673248,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000238145.2","gene_symbol":"AL731892.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46891639,"end":46892830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180425.11","gene_symbol":"C11orf71","gene_name":"chromosome 11 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:25937]","synonyms":"FLJ20010","biotype":"protein_coding","ncbi_id":"54494","summary":null,"start":114391443,"end":114400511,"strand":-1,"description":"chromosome 11 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:25937]"}, {"versioned_ensembl_gene_id":"ENSG00000261546.1","gene_symbol":"AC135782.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89113175,"end":89115279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143702.15","gene_symbol":"CEP170","gene_name":"centrosomal protein 170 [Source:HGNC Symbol;Acc:HGNC:28920]","synonyms":"KAB,FAM68A,KIAA0470","biotype":"protein_coding","ncbi_id":"9859","summary":"The product of this gene is a component of the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. During interphase, the encoded protein localizes to the sub-distal appendages of mature centrioles, which are microtubule-based structures thought to help organize centrosomes. During mitosis, the protein associates with spindle microtubules near the centrosomes. The protein interacts with and is phosphorylated by polo-like kinase 1, and functions in maintaining microtubule organization and cell morphology. The human genome contains a putative transcribed pseudogene. Several alternatively spliced transcript variants of this gene have been found, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":243124428,"end":243255348,"strand":-1,"description":"centrosomal protein 170 [Source:HGNC Symbol;Acc:HGNC:28920]"}, {"versioned_ensembl_gene_id":"ENSG00000215571.5","gene_symbol":"GRK6P1","gene_name":"G protein-coupled receptor kinase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4547]","synonyms":"GRK6PS,GPRK6P,GPRK6L","biotype":"processed_pseudogene","ncbi_id":"2871","summary":null,"start":21319156,"end":21320866,"strand":1,"description":"G protein-coupled receptor kinase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4547]"}, {"versioned_ensembl_gene_id":"ENSG00000267646.1","gene_symbol":"AC008543.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11796084,"end":11798598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227230.1","gene_symbol":"AL606534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":243135898,"end":243140588,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244244.2","gene_symbol":"AP000805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92498152,"end":92498935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164076.16","gene_symbol":"CAMKV","gene_name":"CaM kinase like vesicle associated [Source:HGNC Symbol;Acc:HGNC:28788]","synonyms":"VACAMKL,MGC8407","biotype":"protein_coding","ncbi_id":"79012","summary":null,"start":49857988,"end":49870222,"strand":-1,"description":"CaM kinase like vesicle associated [Source:HGNC Symbol;Acc:HGNC:28788]"}, {"versioned_ensembl_gene_id":"ENSG00000177599.12","gene_symbol":"ZNF491","gene_name":"zinc finger protein 491 [Source:HGNC Symbol;Acc:HGNC:23706]","synonyms":"FLJ34791","biotype":"protein_coding","ncbi_id":"126069","summary":null,"start":11797667,"end":11809622,"strand":1,"description":"zinc finger protein 491 [Source:HGNC Symbol;Acc:HGNC:23706]"}, {"versioned_ensembl_gene_id":"ENSG00000114767.6","gene_symbol":"RRP9","gene_name":"ribosomal RNA processing 9, U3 small nucleolar RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16829]","synonyms":"U3-55K,RNU3IP2","biotype":"protein_coding","ncbi_id":"9136","summary":"This gene encodes a member of the WD-repeat protein family. The encoded protein is a component of the nucleolar small nuclear ribonucleoprotein particle (snoRNP) and is essential for 18s rRNA processing during ribosome synthesis. It contains seven WD domains required for nucleolar localization and specific interaction with the U3 small nucleolar RNA (U3 snoRNA). [provided by RefSeq, Oct 2012]","start":51933430,"end":51941941,"strand":-1,"description":"ribosomal RNA processing 9, U3 small nucleolar RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16829]"}, {"versioned_ensembl_gene_id":"ENSG00000231254.2","gene_symbol":"PCED1CP","gene_name":"PC-esterase domain containing 1C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44083]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646249","summary":null,"start":212832161,"end":212832945,"strand":1,"description":"PC-esterase domain containing 1C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44083]"}, {"versioned_ensembl_gene_id":"ENSG00000141337.12","gene_symbol":"ARSG","gene_name":"arylsulfatase G [Source:HGNC Symbol;Acc:HGNC:24102]","synonyms":"KIAA1001","biotype":"protein_coding","ncbi_id":"22901","summary":"The protein encoded by this gene belongs to the sulfatase enzyme family. Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules. This protein displays arylsulfatase activity at acidic pH, as is typical of lysosomal sulfatases, and has been shown to localize in the lysosomes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]","start":68259182,"end":68422731,"strand":1,"description":"arylsulfatase G [Source:HGNC Symbol;Acc:HGNC:24102]"}, {"versioned_ensembl_gene_id":"ENSG00000173372.16","gene_symbol":"C1QA","gene_name":"complement C1q A chain [Source:HGNC Symbol;Acc:HGNC:1241]","synonyms":null,"biotype":"protein_coding","ncbi_id":"712","summary":"This gene encodes the A-chain polypeptide of serum complement subcomponent C1q, which associates with C1r and C1s to yield the first component of the serum complement system. C1q deficiency is associated with lupus erythematosus and glomerulonephritis. C1q is composed of 18 polypeptide chains which include 6 A-chains, 6 B-chains, and 6 C-chains. Each chain contains an N-terminal collagen-like region and a C-terminal C1q globular domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":22636506,"end":22639608,"strand":1,"description":"complement C1q A chain [Source:HGNC Symbol;Acc:HGNC:1241]"}, {"versioned_ensembl_gene_id":"ENSG00000270306.1","gene_symbol":"AL158050.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51385282,"end":51385849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229757.2","gene_symbol":"AL031736.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168578653,"end":168579439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175220.11","gene_symbol":"ARHGAP1","gene_name":"Rho GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:673]","synonyms":"RhoGAP,p50rhoGAP,CDC42GAP","biotype":"protein_coding","ncbi_id":"392","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein contains a SRC homology 3 domain and interacts with Bcl-2-associated protein family members. [provided by RefSeq, Aug 2012]","start":46677080,"end":46700615,"strand":-1,"description":"Rho GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:673]"}, {"versioned_ensembl_gene_id":"ENSG00000223861.1","gene_symbol":"AL365436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151557446,"end":151557940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159596.6","gene_symbol":"TMEM69","gene_name":"transmembrane protein 69 [Source:HGNC Symbol;Acc:HGNC:28035]","synonyms":"FLJ21029,C1orf154","biotype":"protein_coding","ncbi_id":"51249","summary":null,"start":45687214,"end":45694443,"strand":1,"description":"transmembrane protein 69 [Source:HGNC Symbol;Acc:HGNC:28035]"}, {"versioned_ensembl_gene_id":"ENSG00000229222.1","gene_symbol":"KRT18P4","gene_name":"keratin 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16604]","synonyms":"OTTHUMG00000032705,dJ963K23.1","biotype":"processed_pseudogene","ncbi_id":"391256","summary":null,"start":49956745,"end":49958032,"strand":1,"description":"keratin 18 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16604]"}, {"versioned_ensembl_gene_id":"ENSG00000232965.1","gene_symbol":"RPS12P18","gene_name":"ribosomal protein S12 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271354","summary":null,"start":79544087,"end":79544356,"strand":1,"description":"ribosomal protein S12 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36421]"}, {"versioned_ensembl_gene_id":"ENSG00000163808.16","gene_symbol":"KIF15","gene_name":"kinesin family member 15 [Source:HGNC Symbol;Acc:HGNC:17273]","synonyms":"NY-BR-62,KNSL7,HKLP2","biotype":"protein_coding","ncbi_id":"56992","summary":null,"start":44761717,"end":44873376,"strand":1,"description":"kinesin family member 15 [Source:HGNC Symbol;Acc:HGNC:17273]"}, {"versioned_ensembl_gene_id":"ENSG00000227777.1","gene_symbol":"AL031736.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":168542737,"end":168543354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277575.1","gene_symbol":"AL162233.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67203635,"end":67208072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102471.13","gene_symbol":"NDFIP2","gene_name":"Nedd4 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:18537]","synonyms":"N4wbp5a,KIAA1165","biotype":"protein_coding","ncbi_id":"54602","summary":null,"start":79481124,"end":79556075,"strand":1,"description":"Nedd4 family interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:18537]"}, {"versioned_ensembl_gene_id":"ENSG00000259840.1","gene_symbol":"Z97653.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":710746,"end":711277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279791.1","gene_symbol":"AC018892.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97094935,"end":97097433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234699.1","gene_symbol":"AL139339.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103452846,"end":103462695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254449.1","gene_symbol":"AP002765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123597946,"end":123599452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266283.1","gene_symbol":"AC091588.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22200619,"end":22205229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214354.3","gene_symbol":"AC133644.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87565828,"end":87566764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274820.1","gene_symbol":"AL353770.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66979460,"end":66979862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274561.1","gene_symbol":"AC005332.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68131462,"end":68131907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257435.1","gene_symbol":"AC087311.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32988763,"end":32993754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274461.1","gene_symbol":"AL391425.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":120819307,"end":120825311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205293.3","gene_symbol":"LINC01602","gene_name":"long intergenic non-protein coding RNA 1602 [Source:HGNC Symbol;Acc:HGNC:51634]","synonyms":"T1560","biotype":"lincRNA","ncbi_id":"100505477","summary":null,"start":57978358,"end":57984126,"strand":1,"description":"long intergenic non-protein coding RNA 1602 [Source:HGNC Symbol;Acc:HGNC:51634]"}, {"versioned_ensembl_gene_id":"ENSG00000271670.1","gene_symbol":"AC010998.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120879256,"end":120880667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214222.2","gene_symbol":"TUBBP2","gene_name":"tubulin beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12415]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647000","summary":null,"start":41384773,"end":41385183,"strand":-1,"description":"tubulin beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12415]"}, {"versioned_ensembl_gene_id":"ENSG00000280085.1","gene_symbol":"AP001002.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90972316,"end":90972521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227574.2","gene_symbol":"AC112229.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110449242,"end":110451064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279361.1","gene_symbol":"AC079331.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67637774,"end":67638973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237731.1","gene_symbol":"RNGTTP1","gene_name":"RNA guanylyltransferase and 5'-phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39652]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421428","summary":null,"start":25643489,"end":25644216,"strand":1,"description":"RNA guanylyltransferase and 5'-phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39652]"}, {"versioned_ensembl_gene_id":"ENSG00000184115.17","gene_symbol":"AC112229.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110397406,"end":110435166,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214552.4","gene_symbol":"COPS8P2","gene_name":"COP9 signalosome subunit 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45270]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"375350","summary":null,"start":68145004,"end":68145630,"strand":1,"description":"COP9 signalosome subunit 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45270]"}, {"versioned_ensembl_gene_id":"ENSG00000259989.1","gene_symbol":"AC135782.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88984032,"end":88995369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214223.4","gene_symbol":"HNRNPA1P10","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39128]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"664709","summary":null,"start":11666069,"end":11667030,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39128]"}, {"versioned_ensembl_gene_id":"ENSG00000267500.1","gene_symbol":"ZNF887P","gene_name":"zinc finger protein 887, pseudogene [Source:HGNC Symbol;Acc:HGNC:38700]","synonyms":"ZNF887","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100419709","summary":null,"start":11648364,"end":11652877,"strand":1,"description":"zinc finger protein 887, pseudogene [Source:HGNC Symbol;Acc:HGNC:38700]"}, {"versioned_ensembl_gene_id":"ENSG00000081277.12","gene_symbol":"PKP1","gene_name":"plakophilin 1 [Source:HGNC Symbol;Acc:HGNC:9023]","synonyms":"B6P","biotype":"protein_coding","ncbi_id":"5317","summary":"This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may be involved in molecular recruitment and stabilization during desmosome formation. Mutations in this gene have been associated with the ectodermal dysplasia/skin fragility syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":201283452,"end":201332993,"strand":1,"description":"plakophilin 1 [Source:HGNC Symbol;Acc:HGNC:9023]"}, {"versioned_ensembl_gene_id":"ENSG00000215867.4","gene_symbol":"KRT18P57","gene_name":"keratin 18 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:48884]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643329","summary":null,"start":111648291,"end":111649544,"strand":-1,"description":"keratin 18 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:48884]"}, {"versioned_ensembl_gene_id":"ENSG00000073670.13","gene_symbol":"ADAM11","gene_name":"ADAM metallopeptidase domain 11 [Source:HGNC Symbol;Acc:HGNC:189]","synonyms":"MDC","biotype":"protein_coding","ncbi_id":"4185","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease) protein family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature protease. This gene represents a candidate tumor suppressor gene for human breast cancer based on its location within a minimal region of chromosome 17q21 previously defined by tumor deletion mapping. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":44759031,"end":44781846,"strand":1,"description":"ADAM metallopeptidase domain 11 [Source:HGNC Symbol;Acc:HGNC:189]"}, {"versioned_ensembl_gene_id":"ENSG00000224952.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"G17,PBX2MHC,HOX12","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32192405,"end":32197856,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000104331.8","gene_symbol":"IMPAD1","gene_name":"inositol monophosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26019]","synonyms":"IMPA3,gPAPP,FLJ20421","biotype":"protein_coding","ncbi_id":"54928","summary":"This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]","start":56957933,"end":56993844,"strand":-1,"description":"inositol monophosphatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26019]"}, {"versioned_ensembl_gene_id":"ENSG00000256612.7","gene_symbol":"CYP2B7P","gene_name":"cytochrome P450 family 2 subfamily B member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:2616]","synonyms":"CYP2B7P1,CYP2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1556","summary":null,"start":40924219,"end":40950660,"strand":1,"description":"cytochrome P450 family 2 subfamily B member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:2616]"}, {"versioned_ensembl_gene_id":"ENSG00000244693.1","gene_symbol":"CTAGE8","gene_name":"CTAGE family member 8 [Source:HGNC Symbol;Acc:HGNC:37294]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100142659","summary":null,"start":144266701,"end":144269288,"strand":-1,"description":"CTAGE family member 8 [Source:HGNC Symbol;Acc:HGNC:37294]"}, {"versioned_ensembl_gene_id":"ENSG00000241431.1","gene_symbol":"RPL37P6","gene_name":"ribosomal protein L37 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31080]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"346950","summary":null,"start":56588385,"end":56588787,"strand":1,"description":"ribosomal protein L37 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31080]"}, {"versioned_ensembl_gene_id":"ENSG00000173080.5","gene_symbol":"RXFP4","gene_name":"relaxin/insulin like family peptide receptor 4 [Source:HGNC Symbol;Acc:HGNC:14666]","synonyms":"RLN3R2,GPR100,GPCR142,RXFPR4","biotype":"protein_coding","ncbi_id":"339403","summary":"GPR100 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003 [PubMed 14623098]).[supplied by OMIM, Mar 2008]","start":155941710,"end":155942949,"strand":1,"description":"relaxin/insulin like family peptide receptor 4 [Source:HGNC Symbol;Acc:HGNC:14666]"}, {"versioned_ensembl_gene_id":"ENSG00000254758.1","gene_symbol":"AP000889.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":107642887,"end":107643871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278765.1","gene_symbol":"AC004477.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48066704,"end":48067293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275094.1","gene_symbol":"AC079395.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":97000436,"end":97001593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253449.1","gene_symbol":"AC025437.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158225352,"end":158234376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272323.1","gene_symbol":"AC026801.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34837549,"end":34839278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237031.7","gene_symbol":"AC008067.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80572681,"end":80618777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229569.1","gene_symbol":"AL356753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79000484,"end":79003803,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258595.2","gene_symbol":"AL110118.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93138066,"end":93138465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189099.11","gene_symbol":"PRSS48","gene_name":"protease, serine 48 [Source:HGNC Symbol;Acc:HGNC:24635]","synonyms":"ESSPL","biotype":"protein_coding","ncbi_id":"345062","summary":null,"start":151277171,"end":151291453,"strand":1,"description":"protease, serine 48 [Source:HGNC Symbol;Acc:HGNC:24635]"}, {"versioned_ensembl_gene_id":"ENSG00000185774.14","gene_symbol":"KCNIP4","gene_name":"potassium voltage-gated channel interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30083]","synonyms":"MGC44947,KCHIP4,CALP","biotype":"protein_coding","ncbi_id":"80333","summary":"This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have EF-hand-like domains, and differ from each other in the N-terminus. They are integral subunit components of native Kv4 channel complexes. They may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. This protein member also interacts with presenilin. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":20728616,"end":21948799,"strand":-1,"description":"potassium voltage-gated channel interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30083]"}, {"versioned_ensembl_gene_id":"ENSG00000272995.1","gene_symbol":"AC097505.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20766808,"end":20767372,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254230.1","gene_symbol":"AC037459.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22565997,"end":22567171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181381.13","gene_symbol":"DDX60L","gene_name":"DEAD-box helicase 60 like [Source:HGNC Symbol;Acc:HGNC:26429]","synonyms":"FLJ31033","biotype":"protein_coding","ncbi_id":"91351","summary":"This gene encodes a member of the DExD/H-box helicase family of proteins, a subset of the super family 2 helicases. Members of the DExD/H-box helicase family share a conserved functional core comprised of two RecA-like globular domains. These domains contain conserved motifs that mediate ATP binding, ATP hydrolysis, nucleic acid binding, and RNA unwinding. In addition to functions in RNA metabolism, members of this family are involved in anti-viral immunity and act as cytosolic sensors of viral nucleic acids. The protein encoded by this gene has been shown to inhibit hepatitis C virus replication in response to interferon stimulation in cell culture. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":168356735,"end":168537786,"strand":-1,"description":"DEAD-box helicase 60 like [Source:HGNC Symbol;Acc:HGNC:26429]"}, {"versioned_ensembl_gene_id":"ENSG00000136436.14","gene_symbol":"CALCOCO2","gene_name":"calcium binding and coiled-coil domain 2 [Source:HGNC Symbol;Acc:HGNC:29912]","synonyms":"NDP52,MGC17318","biotype":"protein_coding","ncbi_id":"10241","summary":"This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a receptor for ubiquitin-coated bacteria and plays an important role in innate immunity by mediating macroautophagy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":48830988,"end":48866522,"strand":1,"description":"calcium binding and coiled-coil domain 2 [Source:HGNC Symbol;Acc:HGNC:29912]"}, {"versioned_ensembl_gene_id":"ENSG00000133958.13","gene_symbol":"UNC79","gene_name":"unc-79 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:19966]","synonyms":"KIAA1409","biotype":"protein_coding","ncbi_id":"57578","summary":"The NALCN channel is responsible for Na(+) leak currents. The protein encoded by this gene, along with UNC80, is an accessory subunit of the NALCN channel that contributes to the Ca(2+) sensitivity of the channel. [provided by RefSeq, Sep 2016]","start":93333219,"end":93707876,"strand":1,"description":"unc-79 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:19966]"}, {"versioned_ensembl_gene_id":"ENSG00000254400.1","gene_symbol":"AC091564.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6603642,"end":6604420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267589.1","gene_symbol":"AC011444.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6072823,"end":6073527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128626.11","gene_symbol":"MRPS12","gene_name":"mitochondrial ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10380]","synonyms":"RPSM12,RPS12,RPMS12","biotype":"protein_coding","ncbi_id":"6183","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S12P family. The encoded protein is a key component of the ribosomal small subunit and controls the decoding fidelity and susceptibility to aminoglycoside antibiotics. The gene for mitochondrial seryl-tRNA synthetase is located upstream and adjacent to this gene, and both genes are possible candidates for the autosomal dominant deafness gene (DFNA4). Splice variants that differ in the 5' UTR have been found for this gene; all three variants encode the same protein. [provided by RefSeq, Jul 2008]","start":38930548,"end":38933162,"strand":1,"description":"mitochondrial ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10380]"}, {"versioned_ensembl_gene_id":"ENSG00000135218.17","gene_symbol":"CD36","gene_name":"CD36 molecule [Source:HGNC Symbol;Acc:HGNC:1663]","synonyms":"GPIV,GP4,GP3B,FAT,SCARB3","biotype":"protein_coding","ncbi_id":"948","summary":"The protein encoded by this gene is the fourth major glycoprotein of the platelet surface and serves as a receptor for thrombospondin in platelets and various cell lines. Since thrombospondins are widely distributed proteins involved in a variety of adhesive processes, this protein may have important functions as a cell adhesion molecule. It binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL. It directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes and it binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport. Mutations in this gene cause platelet glycoprotein deficiency. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2014]","start":80369575,"end":80679277,"strand":1,"description":"CD36 molecule [Source:HGNC Symbol;Acc:HGNC:1663]"}, {"versioned_ensembl_gene_id":"ENSG00000279920.1","gene_symbol":"LINC01651","gene_name":"long intergenic non-protein coding RNA 1651 [Source:HGNC Symbol;Acc:HGNC:52439]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372944","summary":null,"start":21354563,"end":21355763,"strand":1,"description":"long intergenic non-protein coding RNA 1651 [Source:HGNC Symbol;Acc:HGNC:52439]"}, {"versioned_ensembl_gene_id":"ENSG00000174678.9","gene_symbol":"FAM47DP","gene_name":"family with sequence similarity 47 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:34342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139249","summary":null,"start":37541077,"end":37545262,"strand":-1,"description":"family with sequence similarity 47 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:34342]"}, {"versioned_ensembl_gene_id":"ENSG00000235774.1","gene_symbol":"AC023347.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126308510,"end":126343992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166181.12","gene_symbol":"API5","gene_name":"apoptosis inhibitor 5 [Source:HGNC Symbol;Acc:HGNC:594]","synonyms":"API5L1,AAC11,AAC-11","biotype":"protein_coding","ncbi_id":"8539","summary":"This gene encodes an apoptosis inhibitory protein whose expression prevents apoptosis after growth factor deprivation. This protein suppresses the transcription factor E2F1-induced apoptosis and also interacts with, and negatively regulates Acinus, a nuclear factor involved in apoptotic DNA fragmentation. Its depletion enhances the cytotoxic action of the chemotherapeutic drugs. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":43311963,"end":43344529,"strand":1,"description":"apoptosis inhibitor 5 [Source:HGNC Symbol;Acc:HGNC:594]"}, {"versioned_ensembl_gene_id":"ENSG00000254927.1","gene_symbol":"AC027779.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13826843,"end":13879499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279891.1","gene_symbol":"FLJ42393","gene_name":"uncharacterized LOC401105 [Source:NCBI gene;Acc:401105]","synonyms":"AVPC1948","biotype":"TEC","ncbi_id":"401105","summary":null,"start":188178543,"end":188180812,"strand":1,"description":"uncharacterized LOC401105 [Source:NCBI gene;Acc:401105]"}, {"versioned_ensembl_gene_id":"ENSG00000085365.17","gene_symbol":"SCAMP1","gene_name":"secretory carrier membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:10563]","synonyms":"SCAMP37","biotype":"protein_coding","ncbi_id":"9522","summary":"This gene product belongs to the SCAMP family of proteins, which are secretory carrier membrane proteins. They function as carriers to the cell surface in post-golgi recycling pathways. Different family members are highly related products of distinct genes, and are usually expressed together. These findings suggest that these protein family members may function at the same site during vesicular transport rather than in separate pathways. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":78360583,"end":78479071,"strand":1,"description":"secretory carrier membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:10563]"}, {"versioned_ensembl_gene_id":"ENSG00000249685.1","gene_symbol":"AC079921.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39133913,"end":39135608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231814.2","gene_symbol":"LINC00210","gene_name":"long intergenic non-protein coding RNA 210 [Source:HGNC Symbol;Acc:HGNC:37458]","synonyms":"RP11-72L13.1,NCRNA00210","biotype":"lincRNA","ncbi_id":"100885798","summary":null,"start":217892900,"end":217920804,"strand":1,"description":"long intergenic non-protein coding RNA 210 [Source:HGNC Symbol;Acc:HGNC:37458]"}, {"versioned_ensembl_gene_id":"ENSG00000234238.1","gene_symbol":"AC022498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188107096,"end":188147020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260052.1","gene_symbol":"AC023813.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48637143,"end":48638719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274628.4","gene_symbol":"AL669942.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":66047084,"end":66055006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260086.2","gene_symbol":"AC007611.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48623436,"end":48744921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236412.1","gene_symbol":"AC092941.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188001700,"end":188003406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258394.1","gene_symbol":"AL442163.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":42362983,"end":42703655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231878.1","gene_symbol":"SNRPFP1","gene_name":"small nuclear ribonucleoprotein polypeptide F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16551]","synonyms":"dJ1041C10.2","biotype":"processed_pseudogene","ncbi_id":"170550","summary":null,"start":49729591,"end":49729842,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16551]"}, {"versioned_ensembl_gene_id":"ENSG00000219755.1","gene_symbol":"AL137784.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99575712,"end":99576456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237557.1","gene_symbol":"YWHABP1","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50294]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647051","summary":null,"start":38643042,"end":38643768,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50294]"}, {"versioned_ensembl_gene_id":"ENSG00000225585.1","gene_symbol":"IPPKP1","gene_name":"inositol 1,3,4,5,6-pentakisphosphate 2-kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39390]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874419","summary":null,"start":21103003,"end":21104371,"strand":-1,"description":"inositol 1,3,4,5,6-pentakisphosphate 2-kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39390]"}, {"versioned_ensembl_gene_id":"ENSG00000254475.1","gene_symbol":"OR2AT1P","gene_name":"olfactory receptor family 2 subfamily AT member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15145]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390225","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":75131138,"end":75131880,"strand":-1,"description":"olfactory receptor family 2 subfamily AT member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15145]"}, {"versioned_ensembl_gene_id":"ENSG00000147761.8","gene_symbol":"TTTY7B","gene_name":"testis-specific transcript, Y-linked 7B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37463]","synonyms":"NCRNA00215","biotype":"lincRNA","ncbi_id":"100101120","summary":null,"start":9706824,"end":9715262,"strand":-1,"description":"testis-specific transcript, Y-linked 7B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37463]"}, {"versioned_ensembl_gene_id":"ENSG00000227128.4","gene_symbol":"LBX1-AS1","gene_name":"LBX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48678]","synonyms":"FLJ41350","biotype":"processed_transcript","ncbi_id":"399806","summary":null,"start":101229594,"end":101270148,"strand":1,"description":"LBX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48678]"}, {"versioned_ensembl_gene_id":"ENSG00000150093.18","gene_symbol":"ITGB1","gene_name":"integrin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6153]","synonyms":"MSK12,MDF2,GPIIA,FNRB,CD29","biotype":"protein_coding","ncbi_id":"3688","summary":"Integrins are heterodimeric proteins made up of alpha and beta subunits. At least 18 alpha and 8 beta subunits have been described in mammals. Integrin family members are membrane receptors involved in cell adhesion and recognition in a variety of processes including embryogenesis, hemostasis, tissue repair, immune response and metastatic diffusion of tumor cells. This gene encodes a beta subunit. Multiple alternatively spliced transcript variants which encode different protein isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32900319,"end":33005792,"strand":-1,"description":"integrin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6153]"}, {"versioned_ensembl_gene_id":"ENSG00000229878.1","gene_symbol":"AL365203.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33035469,"end":33035664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100346.17","gene_symbol":"CACNA1I","gene_name":"calcium voltage-gated channel subunit alpha1 I [Source:HGNC Symbol;Acc:HGNC:1396]","synonyms":"Cav3.3","biotype":"protein_coding","ncbi_id":"8911","summary":"This gene encodes the pore-forming alpha subunit of a voltage gated calcium channel. The encoded protein is a member of a subfamily of calcium channels referred to as is a low voltage-activated, T-type, calcium channel. The channel encoded by this protein is characterized by a slower activation and inactivation compared to other T-type calcium channels. This protein may be involved in calcium signaling in neurons. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":39570753,"end":39689737,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 I [Source:HGNC Symbol;Acc:HGNC:1396]"}, {"versioned_ensembl_gene_id":"ENSG00000148334.14","gene_symbol":"PTGES2","gene_name":"prostaglandin E synthase 2 [Source:HGNC Symbol;Acc:HGNC:17822]","synonyms":"FLJ14038,C9orf15","biotype":"protein_coding","ncbi_id":"80142","summary":"The protein encoded by this gene is a membrane-associated prostaglandin E synthase, which catalyzes the conversion of prostaglandin H2 to prostaglandin E2. This protein also has been shown to activate the transcription regulated by a gamma-interferon-activated transcription element (GATE). Multiple transcript variants have been found for this gene. [provided by RefSeq, Jun 2009]","start":128120693,"end":128128462,"strand":-1,"description":"prostaglandin E synthase 2 [Source:HGNC Symbol;Acc:HGNC:17822]"}, {"versioned_ensembl_gene_id":"ENSG00000184774.9","gene_symbol":"MGAT4EP","gene_name":"MGAT4 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:49418]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"641515","summary":null,"start":202820266,"end":202827225,"strand":1,"description":"MGAT4 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:49418]"}, {"versioned_ensembl_gene_id":"ENSG00000258901.2","gene_symbol":"AL121821.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41555662,"end":41556055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085733.15","gene_symbol":"CTTN","gene_name":"cortactin [Source:HGNC Symbol;Acc:HGNC:3338]","synonyms":"EMS1","biotype":"protein_coding","ncbi_id":"2017","summary":"This gene is overexpressed in breast cancer and squamous cell carcinomas of the head and neck. The encoded protein is localized in the cytoplasm and in areas of the cell-substratum contacts. This gene has two roles: (1) regulating the interactions between components of adherens-type junctions and (2) organizing the cytoskeleton and cell adhesion structures of epithelia and carcinoma cells. During apoptosis, the encoded protein is degraded in a caspase-dependent manner. The aberrant regulation of this gene contributes to tumor cell invasion and metastasis. Three splice variants that encode different isoforms have been identified for this gene. [provided by RefSeq, May 2010]","start":70398404,"end":70436584,"strand":1,"description":"cortactin [Source:HGNC Symbol;Acc:HGNC:3338]"}, {"versioned_ensembl_gene_id":"ENSG00000215760.2","gene_symbol":"TAF9BP2","gene_name":"TATA-box binding protein associated factor 9b pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38836]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130319","summary":null,"start":114809375,"end":114811170,"strand":1,"description":"TATA-box binding protein associated factor 9b pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38836]"}, {"versioned_ensembl_gene_id":"ENSG00000218565.2","gene_symbol":"AL592429.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139338018,"end":139339580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229674.1","gene_symbol":"AL121578.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37994344,"end":37994790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246889.2","gene_symbol":"AP000487.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70372246,"end":70398488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167578.17","gene_symbol":"RAB4B","gene_name":"RAB4B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9782]","synonyms":"MGC52123,FLJ78649","biotype":"protein_coding","ncbi_id":"53916","summary":"RAB proteins, such as RAB4B, are members of the RAS superfamily of small GTPases that are involved in vesicular trafficking (He et al., 2002 [PubMed 12450215]).[supplied by OMIM, Aug 2009]","start":40778216,"end":40796938,"strand":1,"description":"RAB4B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9782]"}, {"versioned_ensembl_gene_id":"ENSG00000267698.1","gene_symbol":"AC002116.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36014508,"end":36045972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258538.5","gene_symbol":"AL133279.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88175391,"end":88180198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163630.10","gene_symbol":"SYNPR","gene_name":"synaptoporin [Source:HGNC Symbol;Acc:HGNC:16507]","synonyms":"SPO,MGC26651","biotype":"protein_coding","ncbi_id":"132204","summary":null,"start":63228315,"end":63616921,"strand":1,"description":"synaptoporin [Source:HGNC Symbol;Acc:HGNC:16507]"}, {"versioned_ensembl_gene_id":"ENSG00000105270.14","gene_symbol":"CLIP3","gene_name":"CAP-Gly domain containing linker protein 3 [Source:HGNC Symbol;Acc:HGNC:24314]","synonyms":"RSNL1,CLIPR-59","biotype":"protein_coding","ncbi_id":"25999","summary":"This gene encodes a member of the cytoplasmic linker protein 170 family. Members of this protein family contain a cytoskeleton-associated protein glycine-rich domain and mediate the interaction of microtubules with cellular organelles. The encoded protein plays a role in T cell apoptosis by facilitating the association of tubulin and the lipid raft ganglioside GD3. The encoded protein also functions as a scaffold protein mediating membrane localization of phosphorylated protein kinase B. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]","start":36014660,"end":36033343,"strand":-1,"description":"CAP-Gly domain containing linker protein 3 [Source:HGNC Symbol;Acc:HGNC:24314]"}, {"versioned_ensembl_gene_id":"ENSG00000268975.1","gene_symbol":"MIA-RAB4B","gene_name":"MIA-RAB4B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48352]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529262","summary":"This locus represents naturally occurring read-through transcription between the neighboring MIA (melanoma inhibitory activity) and RAB4B (RAB4B, member RAS oncogene family) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":40771648,"end":40786685,"strand":1,"description":"MIA-RAB4B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48352]"}, {"versioned_ensembl_gene_id":"ENSG00000228859.2","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"G6c,C6orf24,NG24","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31700817,"end":31704014,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000196115.13","gene_symbol":"ADAM5","gene_name":"ADAM metallopeptidase domain 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:212]","synonyms":"tMDCII,ADAM5P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"255926","summary":null,"start":39314591,"end":39417378,"strand":1,"description":"ADAM metallopeptidase domain 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:212]"}, {"versioned_ensembl_gene_id":"ENSG00000211831.2","gene_symbol":"TRAJ61","gene_name":"T-cell receptor alpha joining 61 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12094]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28694","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22475316,"end":22475375,"strand":1,"description":"T-cell receptor alpha joining 61 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12094]"}, {"versioned_ensembl_gene_id":"ENSG00000249241.1","gene_symbol":"LINC02265","gene_name":"long intergenic non-protein coding RNA 2265 [Source:HGNC Symbol;Acc:HGNC:53179]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060498","summary":null,"start":40316485,"end":40330419,"strand":1,"description":"long intergenic non-protein coding RNA 2265 [Source:HGNC Symbol;Acc:HGNC:53179]"}, {"versioned_ensembl_gene_id":"ENSG00000223997.1","gene_symbol":"TRDD1","gene_name":"T-cell receptor delta diversity 1 [Source:HGNC Symbol;Acc:HGNC:12254]","synonyms":null,"biotype":"TR_D_gene","ncbi_id":"28525","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22438547,"end":22438554,"strand":1,"description":"T-cell receptor delta diversity 1 [Source:HGNC Symbol;Acc:HGNC:12254]"}, {"versioned_ensembl_gene_id":"ENSG00000198853.11","gene_symbol":"RUSC2","gene_name":"RUN and SH3 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23625]","synonyms":"KIAA0375","biotype":"protein_coding","ncbi_id":"9853","summary":"This gene encodes a RUN and SH3 domain containing protein that interacts with Rab1b and Rab1-binding protein GM130. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jun 2012]","start":35490127,"end":35561898,"strand":1,"description":"RUN and SH3 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23625]"}, {"versioned_ensembl_gene_id":"ENSG00000181690.7","gene_symbol":"PLAG1","gene_name":"PLAG1 zinc finger [Source:HGNC Symbol;Acc:HGNC:9045]","synonyms":"ZNF912","biotype":"protein_coding","ncbi_id":"5324","summary":"Pleomorphic adenoma gene 1 encodes a zinc finger protein with 2 putative nuclear localization signals. PLAG1, which is developmentally regulated, has been shown to be consistently rearranged in pleomorphic adenomas of the salivary glands. PLAG1 is activated by the reciprocal chromosomal translocations involving 8q12 in a subset of salivary gland pleomorphic adenomas. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56160904,"end":56211324,"strand":-1,"description":"PLAG1 zinc finger [Source:HGNC Symbol;Acc:HGNC:9045]"}, {"versioned_ensembl_gene_id":"ENSG00000261043.5","gene_symbol":"AC019294.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75759501,"end":75762405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130770.17","gene_symbol":"ATPIF1","gene_name":"ATPase inhibitory factor 1 [Source:HGNC Symbol;Acc:HGNC:871]","synonyms":"MGC1167,IP,ATPIP,ATPI,MGC8898","biotype":"protein_coding","ncbi_id":"93974","summary":"This gene encodes a mitochondrial ATPase inhibitor. Alternative splicing occurs at this locus and three transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":28236109,"end":28246906,"strand":1,"description":"ATPase inhibitory factor 1 [Source:HGNC Symbol;Acc:HGNC:871]"}, {"versioned_ensembl_gene_id":"ENSG00000226486.1","gene_symbol":"LINC01035","gene_name":"long intergenic non-protein coding RNA 1035 [Source:HGNC Symbol;Acc:HGNC:49022]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144592","summary":null,"start":188905688,"end":189037262,"strand":1,"description":"long intergenic non-protein coding RNA 1035 [Source:HGNC Symbol;Acc:HGNC:49022]"}, {"versioned_ensembl_gene_id":"ENSG00000226126.2","gene_symbol":"PSMC1P12","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39787]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644094","summary":null,"start":118614333,"end":118615646,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39787]"}, {"versioned_ensembl_gene_id":"ENSG00000254583.1","gene_symbol":"AC021269.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13478333,"end":13479037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264785.1","gene_symbol":"AC005722.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19737682,"end":19738542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229187.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30459359,"end":30463963,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000224243.1","gene_symbol":"LINC00403","gene_name":"long intergenic non-protein coding RNA 403 [Source:HGNC Symbol;Acc:HGNC:42733]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505996","summary":null,"start":112107119,"end":112108015,"strand":1,"description":"long intergenic non-protein coding RNA 403 [Source:HGNC Symbol;Acc:HGNC:42733]"}, {"versioned_ensembl_gene_id":"ENSG00000251101.1","gene_symbol":"AC147055.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68615393,"end":68616137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149313.10","gene_symbol":"AASDHPPT","gene_name":"aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase [Source:HGNC Symbol;Acc:HGNC:14235]","synonyms":"LYS5,CGI-80,ACPS,AASD-PPT","biotype":"protein_coding","ncbi_id":"60496","summary":"The protein encoded by this gene is similar to Saccharomyces cerevisiae LYS5, which is required for the activation of the alpha-aminoadipate dehydrogenase in the biosynthetic pathway of lysine. Yeast alpha-aminoadipate dehydrogenase converts alpha-biosynthetic-aminoadipate semialdehyde to alpha-aminoadipate. It has been suggested that defects in the human gene result in pipecolic acidemia. [provided by RefSeq, Jul 2008]","start":106075501,"end":106098710,"strand":1,"description":"aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase [Source:HGNC Symbol;Acc:HGNC:14235]"}, {"versioned_ensembl_gene_id":"ENSG00000236133.1","gene_symbol":"LINC01069","gene_name":"long intergenic non-protein coding RNA 1069 [Source:HGNC Symbol;Acc:HGNC:49109]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927176","summary":null,"start":77989372,"end":77990646,"strand":-1,"description":"long intergenic non-protein coding RNA 1069 [Source:HGNC Symbol;Acc:HGNC:49109]"}, {"versioned_ensembl_gene_id":"ENSG00000277043.1","gene_symbol":"EEF1A1P42","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442215","summary":null,"start":49358185,"end":49360420,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:48927]"}, {"versioned_ensembl_gene_id":"ENSG00000211814.1","gene_symbol":"TRAV35","gene_name":"T-cell receptor alpha variable 35 [Source:HGNC Symbol;Acc:HGNC:12134]","synonyms":"TCRAV35S1,TCRAV25S1","biotype":"TR_V_pseudogene","ncbi_id":"28647","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22221896,"end":22222475,"strand":1,"description":"T-cell receptor alpha variable 35 [Source:HGNC Symbol;Acc:HGNC:12134]"}, {"versioned_ensembl_gene_id":"ENSG00000232450.1","gene_symbol":"AL133517.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":113698884,"end":113699631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135314.12","gene_symbol":"KHDC1","gene_name":"KH homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21366]","synonyms":"MGC10818,Em:AC019205.8,C6orf148,C6orf147,bA257K9.4,NDG1","biotype":"protein_coding","ncbi_id":"80759","summary":null,"start":73241314,"end":73310365,"strand":-1,"description":"KH homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21366]"}, {"versioned_ensembl_gene_id":"ENSG00000111335.12","gene_symbol":"OAS2","gene_name":"2'-5'-oligoadenylate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:8087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4939","summary":"This gene encodes a member of the 2-5A synthetase family, essential proteins involved in the innate immune response to viral infection. The encoded protein is induced by interferons and uses adenosine triphosphate in 2'-specific nucleotidyl transfer reactions to synthesize 2',5'-oligoadenylates (2-5As). These molecules activate latent RNase L, which results in viral RNA degradation and the inhibition of viral replication. The three known members of this gene family are located in a cluster on chromosome 12. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":112978395,"end":113011723,"strand":1,"description":"2'-5'-oligoadenylate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:8087]"}, {"versioned_ensembl_gene_id":"ENSG00000224436.1","gene_symbol":"BX323014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":232221938,"end":232222174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132842.13","gene_symbol":"AP3B1","gene_name":"adaptor related protein complex 3 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:566]","synonyms":"ADTB3A,HPS2","biotype":"protein_coding","ncbi_id":"8546","summary":"This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012]","start":78000525,"end":78294755,"strand":-1,"description":"adaptor related protein complex 3 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:566]"}, {"versioned_ensembl_gene_id":"ENSG00000275575.4","gene_symbol":"PTP4A3","gene_name":"protein tyrosine phosphatase type IVA, member 3 [Source:HGNC Symbol;Acc:HGNC:9636]","synonyms":"PRL3,PRL-R,PRL-3","biotype":"protein_coding","ncbi_id":"11156","summary":"This gene encodes a member of the protein-tyrosine phosphatase family. Protein tyrosine phosphatases are cell signaling molecules that play regulatory roles in a variety of cellular processes. Studies of this class of protein tyrosine phosphatase in mice demonstrates that they are prenylated in vivo, suggesting their association with cell plasma membrane. The encoded protein may enhance cell proliferation, and overexpression of this gene has been implicated in tumor metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":141391991,"end":141438356,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 3 [Source:HGNC Symbol;Acc:HGNC:9636]"}, {"versioned_ensembl_gene_id":"ENSG00000089041.16","gene_symbol":"P2RX7","gene_name":"purinergic receptor P2X 7 [Source:HGNC Symbol;Acc:HGNC:8537]","synonyms":"P2X7,MGC20089","biotype":"protein_coding","ncbi_id":"5027","summary":"The product of this gene belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel and is responsible for ATP-dependent lysis of macrophages through the formation of membrane pores permeable to large molecules. Activation of this nuclear receptor by ATP in the cytoplasm may be a mechanism by which cellular activity can be coupled to changes in gene expression. Multiple alternatively spliced variants have been identified, most of which fit nonsense-mediated decay (NMD) criteria. [provided by RefSeq, Jul 2010]","start":121132819,"end":121188032,"strand":1,"description":"purinergic receptor P2X 7 [Source:HGNC Symbol;Acc:HGNC:8537]"}, {"versioned_ensembl_gene_id":"ENSG00000254262.1","gene_symbol":"AC022360.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111742012,"end":111756826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253156.1","gene_symbol":"AC022360.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111621458,"end":111621797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255033.1","gene_symbol":"SERPINA15P","gene_name":"serpin family A member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:44397]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101930744","summary":null,"start":111380603,"end":111380868,"strand":1,"description":"serpin family A member 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:44397]"}, {"versioned_ensembl_gene_id":"ENSG00000234273.1","gene_symbol":"AC073071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109521981,"end":109597166,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229603.1","gene_symbol":"AC004014.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108909453,"end":108952666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158987.20","gene_symbol":"RAPGEF6","gene_name":"Rap guanine nucleotide exchange factor 6 [Source:HGNC Symbol;Acc:HGNC:20655]","synonyms":"PDZ-GEF2,RA-GEF-2,PDZGEF2","biotype":"protein_coding","ncbi_id":"51735","summary":null,"start":131423921,"end":131635236,"strand":-1,"description":"Rap guanine nucleotide exchange factor 6 [Source:HGNC Symbol;Acc:HGNC:20655]"}, {"versioned_ensembl_gene_id":"ENSG00000268985.1","gene_symbol":"AC020908.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17009189,"end":17013460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274333.4","gene_symbol":"CU633967.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5553637,"end":5614880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203970.3","gene_symbol":"DEFB110","gene_name":"defensin beta 110 [Source:HGNC Symbol;Acc:HGNC:18091]","synonyms":"DEFB111,DEFB-11,DEFB-10","biotype":"protein_coding","ncbi_id":"245913","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":50009138,"end":50021981,"strand":-1,"description":"defensin beta 110 [Source:HGNC Symbol;Acc:HGNC:18091]"}, {"versioned_ensembl_gene_id":"ENSG00000229520.1","gene_symbol":"LINC00404","gene_name":"long intergenic non-protein coding RNA 404 [Source:HGNC Symbol;Acc:HGNC:42734]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874160","summary":null,"start":112106095,"end":112106882,"strand":-1,"description":"long intergenic non-protein coding RNA 404 [Source:HGNC Symbol;Acc:HGNC:42734]"}, {"versioned_ensembl_gene_id":"ENSG00000110497.14","gene_symbol":"AMBRA1","gene_name":"autophagy and beclin 1 regulator 1 [Source:HGNC Symbol;Acc:HGNC:25990]","synonyms":"WDR94,KIAA1736,FLJ20294,DCAF3","biotype":"protein_coding","ncbi_id":"55626","summary":null,"start":46396414,"end":46594125,"strand":-1,"description":"autophagy and beclin 1 regulator 1 [Source:HGNC Symbol;Acc:HGNC:25990]"}, {"versioned_ensembl_gene_id":"ENSG00000234377.7","gene_symbol":"RNF219-AS1","gene_name":"RNF219 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42700]","synonyms":"POU4F1-AS1","biotype":"antisense_RNA","ncbi_id":"100874222","summary":null,"start":77919689,"end":78617328,"strand":1,"description":"RNF219 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42700]"}, {"versioned_ensembl_gene_id":"ENSG00000123178.14","gene_symbol":"SPRYD7","gene_name":"SPRY domain containing 7 [Source:HGNC Symbol;Acc:HGNC:14297]","synonyms":"CLLD6,C13orf1","biotype":"protein_coding","ncbi_id":"57213","summary":null,"start":49912706,"end":49936490,"strand":-1,"description":"SPRY domain containing 7 [Source:HGNC Symbol;Acc:HGNC:14297]"}, {"versioned_ensembl_gene_id":"ENSG00000279513.1","gene_symbol":"AL157902.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":117493515,"end":117495006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204351.11","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"SKIV2L1,HLP,SKIV2,DDX13,SKI2W,170A","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31959080,"end":31969755,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000258977.1","gene_symbol":"LINC01467","gene_name":"long intergenic non-protein coding RNA 1467 [Source:HGNC Symbol;Acc:HGNC:50911]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928559","summary":null,"start":81605347,"end":81623061,"strand":-1,"description":"long intergenic non-protein coding RNA 1467 [Source:HGNC Symbol;Acc:HGNC:50911]"}, {"versioned_ensembl_gene_id":"ENSG00000145675.14","gene_symbol":"PIK3R1","gene_name":"phosphoinositide-3-kinase regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:8979]","synonyms":"p85-ALPHA,p85,GRB1","biotype":"protein_coding","ncbi_id":"5295","summary":"Phosphatidylinositol 3-kinase phosphorylates the inositol ring of phosphatidylinositol at the 3-prime position. The enzyme comprises a 110 kD catalytic subunit and a regulatory subunit of either 85, 55, or 50 kD. This gene encodes the 85 kD regulatory subunit. Phosphatidylinositol 3-kinase plays an important role in the metabolic actions of insulin, and a mutation in this gene has been associated with insulin resistance. Alternative splicing of this gene results in four transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]","start":68215720,"end":68301821,"strand":1,"description":"phosphoinositide-3-kinase regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:8979]"}, {"versioned_ensembl_gene_id":"ENSG00000235316.1","gene_symbol":"DUSP8P5","gene_name":"dual specificity phosphatase 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45003]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106903081","summary":null,"start":73731824,"end":73733638,"strand":1,"description":"dual specificity phosphatase 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45003]"}, {"versioned_ensembl_gene_id":"ENSG00000273162.1","gene_symbol":"AL133215.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101060029,"end":101061005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231764.8","gene_symbol":"DLX6-AS1","gene_name":"DLX6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37151]","synonyms":"NCRNA00212,FLJ34048,Evf-2","biotype":"antisense_RNA","ncbi_id":"285987","summary":null,"start":96955141,"end":97014065,"strand":-1,"description":"DLX6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37151]"}, {"versioned_ensembl_gene_id":"ENSG00000196381.10","gene_symbol":"ZNF781","gene_name":"zinc finger protein 781 [Source:HGNC Symbol;Acc:HGNC:26745]","synonyms":"FLJ37549","biotype":"protein_coding","ncbi_id":"163115","summary":null,"start":37667751,"end":37692322,"strand":-1,"description":"zinc finger protein 781 [Source:HGNC Symbol;Acc:HGNC:26745]"}, {"versioned_ensembl_gene_id":"ENSG00000283486.2","gene_symbol":"FAM95C","gene_name":"family with sequence similarity 95 member C [Source:HGNC Symbol;Acc:HGNC:45272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100289137","summary":null,"start":38540569,"end":38577207,"strand":-1,"description":"family with sequence similarity 95 member C [Source:HGNC Symbol;Acc:HGNC:45272]"}, {"versioned_ensembl_gene_id":"ENSG00000206549.13","gene_symbol":"PRSS50","gene_name":"protease, serine 50 [Source:HGNC Symbol;Acc:HGNC:17910]","synonyms":"TSP50,CT20,TSP50,CT20","biotype":"protein_coding","ncbi_id":"29122","summary":null,"start":46712115,"end":46812574,"strand":-1,"description":"protease, serine 50 [Source:HGNC Symbol;Acc:HGNC:17910]"}, {"versioned_ensembl_gene_id":"ENSG00000129351.17","gene_symbol":"ILF3","gene_name":"interleukin enhancer binding factor 3 [Source:HGNC Symbol;Acc:HGNC:6038]","synonyms":"NFAR-1,NF90,MPP4,MPHOSPH4,DRBP76","biotype":"protein_coding","ncbi_id":"3609","summary":"This gene encodes a double-stranded RNA (dsRNA) binding protein that complexes with other proteins, dsRNAs, small noncoding RNAs, and mRNAs to regulate gene expression and stabilize mRNAs. This protein (NF90, ILF3) forms a heterodimer with a 45 kDa transcription factor (NF45, ILF2) required for T-cell expression of interleukin 2. This complex has been shown to affect the redistribution of nuclear mRNA to the cytoplasm. Knockdown of NF45 or NF90 protein retards cell growth, possibly by inhibition of mRNA stabilization. In contrast, an isoform (NF110) of this gene that is predominantly restricted to the nucleus has only minor effects on cell growth when its levels are reduced. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2014]","start":10654261,"end":10692417,"strand":1,"description":"interleukin enhancer binding factor 3 [Source:HGNC Symbol;Acc:HGNC:6038]"}, {"versioned_ensembl_gene_id":"ENSG00000108094.14","gene_symbol":"CUL2","gene_name":"cullin 2 [Source:HGNC Symbol;Acc:HGNC:2552]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8453","summary":null,"start":35008551,"end":35090642,"strand":-1,"description":"cullin 2 [Source:HGNC Symbol;Acc:HGNC:2552]"}, {"versioned_ensembl_gene_id":"ENSG00000247049.2","gene_symbol":"AC008443.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181224646,"end":181230685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250884.1","gene_symbol":"OR7E85P","gene_name":"olfactory receptor family 7 subfamily E member 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:14692]","synonyms":"OR7E88P","biotype":"unprocessed_pseudogene","ncbi_id":"442105","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9483718,"end":9484702,"strand":1,"description":"olfactory receptor family 7 subfamily E member 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:14692]"}, {"versioned_ensembl_gene_id":"ENSG00000230156.2","gene_symbol":"LINC00443","gene_name":"long intergenic non-protein coding RNA 443 [Source:HGNC Symbol;Acc:HGNC:42780]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874173","summary":null,"start":106653916,"end":106672163,"strand":1,"description":"long intergenic non-protein coding RNA 443 [Source:HGNC Symbol;Acc:HGNC:42780]"}, {"versioned_ensembl_gene_id":"ENSG00000233354.1","gene_symbol":"LINC00028","gene_name":"long intergenic non-protein coding RNA 28 [Source:HGNC Symbol;Acc:HGNC:16224]","synonyms":"C20orf93,NCRNA00028,dJ1093G12.6","biotype":"lincRNA","ncbi_id":"140875","summary":null,"start":31485778,"end":31487574,"strand":1,"description":"long intergenic non-protein coding RNA 28 [Source:HGNC Symbol;Acc:HGNC:16224]"}, {"versioned_ensembl_gene_id":"ENSG00000138379.4","gene_symbol":"MSTN","gene_name":"myostatin [Source:HGNC Symbol;Acc:HGNC:4223]","synonyms":"GDF8","biotype":"protein_coding","ncbi_id":"2660","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein negatively regulates skeletal muscle cell proliferation and differentiation. Mutations in this gene are associated with increased skeletal muscle mass in humans and other mammals. [provided by RefSeq, Jul 2016]","start":190055697,"end":190062729,"strand":-1,"description":"myostatin [Source:HGNC Symbol;Acc:HGNC:4223]"}, {"versioned_ensembl_gene_id":"ENSG00000181982.18","gene_symbol":"CCDC149","gene_name":"coiled-coil domain containing 149 [Source:HGNC Symbol;Acc:HGNC:25405]","synonyms":"DKFZp761B107","biotype":"protein_coding","ncbi_id":"91050","summary":null,"start":24806117,"end":24980204,"strand":-1,"description":"coiled-coil domain containing 149 [Source:HGNC Symbol;Acc:HGNC:25405]"}, {"versioned_ensembl_gene_id":"ENSG00000169662.8","gene_symbol":"BCRP6","gene_name":"breakpoint cluster region pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39074]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728468","summary":null,"start":21290760,"end":21294586,"strand":-1,"description":"breakpoint cluster region pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39074]"}, {"versioned_ensembl_gene_id":"ENSG00000256927.1","gene_symbol":"LINC02350","gene_name":"long intergenic non-protein coding RNA 2350 [Source:HGNC Symbol;Acc:HGNC:53272]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370059","summary":null,"start":126425990,"end":126434008,"strand":1,"description":"long intergenic non-protein coding RNA 2350 [Source:HGNC Symbol;Acc:HGNC:53272]"}, {"versioned_ensembl_gene_id":"ENSG00000256494.1","gene_symbol":"AC007368.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126400792,"end":126405528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000001084.10","gene_symbol":"GCLC","gene_name":"glutamate-cysteine ligase catalytic subunit [Source:HGNC Symbol;Acc:HGNC:4311]","synonyms":"GLCLC,GLCL,GCS","biotype":"protein_coding","ncbi_id":"2729","summary":"Glutamate-cysteine ligase, also known as gamma-glutamylcysteine synthetase is the first rate-limiting enzyme of glutathione synthesis. The enzyme consists of two subunits, a heavy catalytic subunit and a light regulatory subunit. This locus encodes the catalytic subunit, while the regulatory subunit is derived from a different gene located on chromosome 1p22-p21. Mutations at this locus have been associated with hemolytic anemia due to deficiency of gamma-glutamylcysteine synthetase and susceptibility to myocardial infarction.[provided by RefSeq, Oct 2010]","start":53497341,"end":53616970,"strand":-1,"description":"glutamate-cysteine ligase catalytic subunit [Source:HGNC Symbol;Acc:HGNC:4311]"}, {"versioned_ensembl_gene_id":"ENSG00000259005.1","gene_symbol":"AC005479.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74474007,"end":74474864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234274.1","gene_symbol":"COX7BP2","gene_name":"cytochrome c oxidase subunit 7B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16601]","synonyms":"dJ901O8.2","biotype":"processed_pseudogene","ncbi_id":"140692","summary":null,"start":35850674,"end":35850915,"strand":-1,"description":"cytochrome c oxidase subunit 7B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16601]"}, {"versioned_ensembl_gene_id":"ENSG00000106331.15","gene_symbol":"PAX4","gene_name":"paired box 4 [Source:HGNC Symbol;Acc:HGNC:8618]","synonyms":"MODY9","biotype":"protein_coding","ncbi_id":"5078","summary":"This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. The paired box 4 gene is involved in pancreatic islet development and mouse studies have demonstrated a role for this gene in differentiation of insulin-producing beta cells. [provided by RefSeq, Jul 2008]","start":127610292,"end":127618114,"strand":-1,"description":"paired box 4 [Source:HGNC Symbol;Acc:HGNC:8618]"}, {"versioned_ensembl_gene_id":"ENSG00000232264.4","gene_symbol":"USP17L24","gene_name":"ubiquitin specific peptidase 17-like family member 24 [Source:HGNC Symbol;Acc:HGNC:44453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728369","summary":null,"start":9325165,"end":9327116,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 24 [Source:HGNC Symbol;Acc:HGNC:44453]"}, {"versioned_ensembl_gene_id":"ENSG00000218261.1","gene_symbol":"AL591034.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53378503,"end":53378861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214812.3","gene_symbol":"AL137792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28120449,"end":28121321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224126.2","gene_symbol":"AC026271.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18677261,"end":18677757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213638.5","gene_symbol":"ADAT3","gene_name":"adenosine deaminase, tRNA specific 3 [Source:HGNC Symbol;Acc:HGNC:25151]","synonyms":"TAD3","biotype":"protein_coding","ncbi_id":"113179","summary":"This gene encodes a subunit of a tRNA-specific adenosine deaminase. This heterodimeric enzyme converts adenosine to inosine in the tRNA anticodon. A mutation in this gene causes a syndrome characterized by intellectual disability and strabismus. This gene shares its 5' exon with the overlapping gene, secretory carrier membrane protein 4 (Gene ID: 113178). [provided by RefSeq, Jul 2016]","start":1905378,"end":1913447,"strand":1,"description":"adenosine deaminase, tRNA specific 3 [Source:HGNC Symbol;Acc:HGNC:25151]"}, {"versioned_ensembl_gene_id":"ENSG00000277675.1","gene_symbol":"AC211486.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75225433,"end":75234310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204472.12","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"AIF-1,IBA1,Em:AF129756.17,IRT-1","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31615184,"end":31617021,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000185838.13","gene_symbol":"GNB1L","gene_name":"G protein subunit beta 1 like [Source:HGNC Symbol;Acc:HGNC:4397]","synonyms":"WDR14,GY2","biotype":"protein_coding","ncbi_id":"54584","summary":"This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008]","start":19783224,"end":19854939,"strand":-1,"description":"G protein subunit beta 1 like [Source:HGNC Symbol;Acc:HGNC:4397]"}, {"versioned_ensembl_gene_id":"ENSG00000189375.10","gene_symbol":"TBC1D28","gene_name":"TBC1 domain family member 28 [Source:HGNC Symbol;Acc:HGNC:26858]","synonyms":"FLJ40244","biotype":"protein_coding","ncbi_id":"254272","summary":null,"start":18635006,"end":18661950,"strand":-1,"description":"TBC1 domain family member 28 [Source:HGNC Symbol;Acc:HGNC:26858]"}, {"versioned_ensembl_gene_id":"ENSG00000139977.13","gene_symbol":"NAA30","gene_name":"N(alpha)-acetyltransferase 30, NatC catalytic subunit [Source:HGNC Symbol;Acc:HGNC:19844]","synonyms":"NAT12,Mak3p,MAK3,FLJ35355,C14orf35","biotype":"protein_coding","ncbi_id":"122830","summary":null,"start":57390544,"end":57415917,"strand":1,"description":"N(alpha)-acetyltransferase 30, NatC catalytic subunit [Source:HGNC Symbol;Acc:HGNC:19844]"}, {"versioned_ensembl_gene_id":"ENSG00000277053.4","gene_symbol":"GTF2IP1","gene_name":"general transcription factor IIi pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4660]","synonyms":"WBSCR7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"2970","summary":null,"start":75185385,"end":75237696,"strand":-1,"description":"general transcription factor IIi pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4660]"}, {"versioned_ensembl_gene_id":"ENSG00000250749.1","gene_symbol":"AC122714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180534184,"end":180534642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262692.1","gene_symbol":"AC116914.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3721628,"end":3722488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251676.1","gene_symbol":"SNHG27","gene_name":"small nucleolar RNA host gene 27 [Source:HGNC Symbol;Acc:HGNC:53481]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927305","summary":null,"start":131773302,"end":131791482,"strand":1,"description":"small nucleolar RNA host gene 27 [Source:HGNC Symbol;Acc:HGNC:53481]"}, {"versioned_ensembl_gene_id":"ENSG00000275834.1","gene_symbol":"AC084368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96306810,"end":96306874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204688.9","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H8,OR2H6,OR6-2","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29457181,"end":29464328,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000138443.15","gene_symbol":"ABI2","gene_name":"abl interactor 2 [Source:HGNC Symbol;Acc:HGNC:24011]","synonyms":"SSH3BP2,argBPIA,AIP-1,AblBP3,ABI2B,ABI-2","biotype":"protein_coding","ncbi_id":"10152","summary":null,"start":203328219,"end":203447723,"strand":1,"description":"abl interactor 2 [Source:HGNC Symbol;Acc:HGNC:24011]"}, {"versioned_ensembl_gene_id":"ENSG00000248184.1","gene_symbol":"LINC02283","gene_name":"long intergenic non-protein coding RNA 2283 [Source:HGNC Symbol;Acc:HGNC:53200]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377656","summary":null,"start":54332892,"end":54355954,"strand":1,"description":"long intergenic non-protein coding RNA 2283 [Source:HGNC Symbol;Acc:HGNC:53200]"}, {"versioned_ensembl_gene_id":"ENSG00000234228.1","gene_symbol":"NCLP2","gene_name":"nucleolin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35473]","synonyms":"bA85L21.1","biotype":"processed_pseudogene","ncbi_id":"100379142","summary":null,"start":135075136,"end":135076597,"strand":-1,"description":"nucleolin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35473]"}, {"versioned_ensembl_gene_id":"ENSG00000204548.3","gene_symbol":"DEFB121","gene_name":"defensin beta 121 [Source:HGNC Symbol;Acc:HGNC:18101]","synonyms":"DEFB-21","biotype":"protein_coding","ncbi_id":"245934","summary":"This gene encodes a member of the beta subfamily of defensins. Beta-defensins are antimicrobial peptides that protect tissues and organs from infection by a variety of microorganisms. This gene is found in a cluster with other beta-defensin genes on the long arm of chromosome 20. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":31404845,"end":31412838,"strand":-1,"description":"defensin beta 121 [Source:HGNC Symbol;Acc:HGNC:18101]"}, {"versioned_ensembl_gene_id":"ENSG00000168070.11","gene_symbol":"MAJIN","gene_name":"membrane anchored junction protein [Source:HGNC Symbol;Acc:HGNC:27441]","synonyms":"C11orf85","biotype":"protein_coding","ncbi_id":"283129","summary":null,"start":64937517,"end":64972085,"strand":-1,"description":"membrane anchored junction protein [Source:HGNC Symbol;Acc:HGNC:27441]"}, {"versioned_ensembl_gene_id":"ENSG00000226484.2","gene_symbol":"AL606516.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36365626,"end":36440292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282693.1","gene_symbol":"LY6L","gene_name":"lymphocyte antigen 6 family member L [Source:HGNC Symbol;Acc:HGNC:52284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928108","summary":null,"start":143085735,"end":143088278,"strand":1,"description":"lymphocyte antigen 6 family member L [Source:HGNC Symbol;Acc:HGNC:52284]"}, {"versioned_ensembl_gene_id":"ENSG00000242550.5","gene_symbol":"SERPINB10","gene_name":"serpin family B member 10 [Source:HGNC Symbol;Acc:HGNC:8942]","synonyms":"PI10,bomapin","biotype":"protein_coding","ncbi_id":"5273","summary":"This gene is a member of the serpin peptidase inhibitor, clade B family and is found in a cluster of other similar genes on chromosome 18. The protein encoded by this gene appears to help control the regulation of protease functions during hematopoiesis. Variations in this gene may increase the risk of prostate cancer. [provided by RefSeq, Dec 2015]","start":63897174,"end":63936111,"strand":1,"description":"serpin family B member 10 [Source:HGNC Symbol;Acc:HGNC:8942]"}, {"versioned_ensembl_gene_id":"ENSG00000244229.1","gene_symbol":"AC027575.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76834429,"end":76834888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250213.2","gene_symbol":"AC025554.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131112748,"end":131113255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240291.1","gene_symbol":"AL450384.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18513115,"end":18545651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176204.13","gene_symbol":"LRRTM4","gene_name":"leucine rich repeat transmembrane neuronal 4 [Source:HGNC Symbol;Acc:HGNC:19411]","synonyms":"FLJ12568","biotype":"protein_coding","ncbi_id":"80059","summary":null,"start":76747719,"end":77593319,"strand":-1,"description":"leucine rich repeat transmembrane neuronal 4 [Source:HGNC Symbol;Acc:HGNC:19411]"}, {"versioned_ensembl_gene_id":"ENSG00000234100.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29306699,"end":29307664,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000259346.2","gene_symbol":"AC105129.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65301922,"end":65302311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234177.5","gene_symbol":"LINC01114","gene_name":"long intergenic non-protein coding RNA 1114 [Source:HGNC Symbol;Acc:HGNC:49245]","synonyms":"PANCAT,LOC284998","biotype":"lincRNA","ncbi_id":"284998","summary":null,"start":104746638,"end":104757719,"strand":-1,"description":"long intergenic non-protein coding RNA 1114 [Source:HGNC Symbol;Acc:HGNC:49245]"}, {"versioned_ensembl_gene_id":"ENSG00000173679.2","gene_symbol":"OR1L1","gene_name":"olfactory receptor family 1 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:8213]","synonyms":"OR9-C,OR1L2","biotype":"protein_coding","ncbi_id":"26737","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122661566,"end":122662648,"strand":1,"description":"olfactory receptor family 1 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:8213]"}, {"versioned_ensembl_gene_id":"ENSG00000160408.14","gene_symbol":"ST6GALNAC6","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:23364]","synonyms":"ST6GALNACVI,SIAT7F","biotype":"protein_coding","ncbi_id":"30815","summary":"ST6GALNAC6 belongs to a family of sialyltransferases that modify proteins and ceramides on the cell surface to alter cell-cell or cell-extracellular matrix interactions (Tsuchida et al., 2003 [PubMed 12668675]).[supplied by OMIM, Mar 2008]","start":127885321,"end":127905408,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:23364]"}, {"versioned_ensembl_gene_id":"ENSG00000171496.4","gene_symbol":"OR1L8","gene_name":"olfactory receptor family 1 subfamily L member 8 [Source:HGNC Symbol;Acc:HGNC:15110]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138881","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122567117,"end":122583384,"strand":-1,"description":"olfactory receptor family 1 subfamily L member 8 [Source:HGNC Symbol;Acc:HGNC:15110]"}, {"versioned_ensembl_gene_id":"ENSG00000179262.9","gene_symbol":"RAD23A","gene_name":"RAD23 homolog A, nucleotide excision repair protein [Source:HGNC Symbol;Acc:HGNC:9812]","synonyms":"MGC111083,HHR23A","biotype":"protein_coding","ncbi_id":"5886","summary":"The protein encoded by this gene is one of two human homologs of Saccharomyces cerevisiae Rad23, a protein involved in nucleotide excision repair. Proteins in this family have a modular domain structure consisting of an ubiquitin-like domain (UbL), ubiquitin-associated domain 1 (UbA1), XPC-binding domain and UbA2. The protein encoded by this gene plays an important role in nucleotide excision repair and also in delivery of polyubiquitinated proteins to the proteasome. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Jun 2012]","start":12945855,"end":12953642,"strand":1,"description":"RAD23 homolog A, nucleotide excision repair protein [Source:HGNC Symbol;Acc:HGNC:9812]"}, {"versioned_ensembl_gene_id":"ENSG00000254722.1","gene_symbol":"FAM8A2P","gene_name":"family with sequence similarity 8 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:16373]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728097","summary":null,"start":56331347,"end":56332488,"strand":-1,"description":"family with sequence similarity 8 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:16373]"}, {"versioned_ensembl_gene_id":"ENSG00000186367.6","gene_symbol":"KIAA1024L","gene_name":"KIAA1024 like [Source:HGNC Symbol;Acc:HGNC:33914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100127206","summary":null,"start":129748079,"end":129766732,"strand":1,"description":"KIAA1024 like [Source:HGNC Symbol;Acc:HGNC:33914]"}, {"versioned_ensembl_gene_id":"ENSG00000262048.1","gene_symbol":"AL078601.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79406240,"end":79406774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185112.5","gene_symbol":"FAM43A","gene_name":"family with sequence similarity 43 member A [Source:HGNC Symbol;Acc:HGNC:26888]","synonyms":"FLJ90022","biotype":"protein_coding","ncbi_id":"131583","summary":null,"start":194686544,"end":194689037,"strand":1,"description":"family with sequence similarity 43 member A [Source:HGNC Symbol;Acc:HGNC:26888]"}, {"versioned_ensembl_gene_id":"ENSG00000254087.7","gene_symbol":"LYN","gene_name":"LYN proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6735]","synonyms":"JTK8","biotype":"protein_coding","ncbi_id":"4067","summary":"This gene encodes a tyrosine protein kinase, which maybe involved in the regulation of mast cell degranulation, and erythroid differentiation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":55879813,"end":56014168,"strand":1,"description":"LYN proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6735]"}, {"versioned_ensembl_gene_id":"ENSG00000128268.11","gene_symbol":"MGAT3","gene_name":"mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7046]","synonyms":"GNT-III","biotype":"protein_coding","ncbi_id":"4248","summary":"There are believed to be over 100 different glycosyltransferases involved in the synthesis of protein-bound and lipid-bound oligosaccharides. The enzyme encoded by this gene transfers a GlcNAc residue to the beta-linked mannose of the trimannosyl core of N-linked oligosaccharides and produces a bisecting GlcNAc. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":39457344,"end":39492194,"strand":1,"description":"mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7046]"}, {"versioned_ensembl_gene_id":"ENSG00000254064.1","gene_symbol":"AC105206.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22254576,"end":22275162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276856.3","gene_symbol":"TUBGCP5","gene_name":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]","synonyms":"KIAA1899,GCP5","biotype":"protein_coding","ncbi_id":"114791","summary":null,"start":22983146,"end":23039654,"strand":-1,"description":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]"}, {"versioned_ensembl_gene_id":"ENSG00000256448.5","gene_symbol":"AP000763.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73405297,"end":73410682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237356.5","gene_symbol":"AL365295.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":53169054,"end":53687258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184428.12","gene_symbol":"TOP1MT","gene_name":"topoisomerase (DNA) I, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116447","summary":"This gene encodes a mitochondrial DNA topoisomerase that plays a role in the modification of DNA topology. The encoded protein is a type IB topoisomerase and catalyzes the transient breaking and rejoining of DNA to relieve tension and DNA supercoiling generated in the mitochondrial genome during replication and transcription. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":143304384,"end":143359979,"strand":-1,"description":"topoisomerase (DNA) I, mitochondrial [Source:HGNC Symbol;Acc:HGNC:29787]"}, {"versioned_ensembl_gene_id":"ENSG00000241744.1","gene_symbol":"AC079953.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101228141,"end":101228876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119004.15","gene_symbol":"CYP20A1","gene_name":"cytochrome P450 family 20 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:20576]","synonyms":"CYP-M","biotype":"protein_coding","ncbi_id":"57404","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein lacks one amino acid of the conserved heme binding site. It also lacks the conserved I-helix motif AGX(D,E)T, suggesting that its substrate may carry its own oxygen. [provided by RefSeq, Jul 2008]","start":203238940,"end":203305611,"strand":1,"description":"cytochrome P450 family 20 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:20576]"}, {"versioned_ensembl_gene_id":"ENSG00000269970.1","gene_symbol":"AL162424.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":122372605,"end":122372825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272170.1","gene_symbol":"AL355385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43074331,"end":43074739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167674.14","gene_symbol":"HDGFL2","gene_name":"HDGF like 2 [Source:HGNC Symbol;Acc:HGNC:14680]","synonyms":"HRP2,Hdgfrp2","biotype":"protein_coding","ncbi_id":"84717","summary":"This gene encodes a member of the hepatoma-derived growth factor (HDGF) family. The protein includes an N-terminal PWWP domain that binds to methyl-lysine-containing histones, with specific binding of this protein to tri-methylated lysines 36 and 79 of histone H3, and di- and tri-methylated lysine 20 of histone H4. The protein functions in LEDGF/p75-independent HIV-1 replication by determining HIV-1 integration site selection. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":4472287,"end":4502211,"strand":1,"description":"HDGF like 2 [Source:HGNC Symbol;Acc:HGNC:14680]"}, {"versioned_ensembl_gene_id":"ENSG00000109208.4","gene_symbol":"SMR3A","gene_name":"submaxillary gland androgen regulated protein 3A [Source:HGNC Symbol;Acc:HGNC:19216]","synonyms":"PROL5,PRL5,PBI","biotype":"protein_coding","ncbi_id":"26952","summary":null,"start":70360761,"end":70367158,"strand":1,"description":"submaxillary gland androgen regulated protein 3A [Source:HGNC Symbol;Acc:HGNC:19216]"}, {"versioned_ensembl_gene_id":"ENSG00000088899.14","gene_symbol":"LZTS3","gene_name":"leucine zipper tumor suppressor family member 3 [Source:HGNC Symbol;Acc:HGNC:30139]","synonyms":"ProSAPiP1,KIAA0552","biotype":"protein_coding","ncbi_id":"9762","summary":null,"start":3162617,"end":3173592,"strand":-1,"description":"leucine zipper tumor suppressor family member 3 [Source:HGNC Symbol;Acc:HGNC:30139]"}, {"versioned_ensembl_gene_id":"ENSG00000182685.7","gene_symbol":"BRICD5","gene_name":"BRICHOS domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28309]","synonyms":"MGC21830,C16orf79","biotype":"protein_coding","ncbi_id":"283870","summary":null,"start":2209253,"end":2211950,"strand":-1,"description":"BRICHOS domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28309]"}, {"versioned_ensembl_gene_id":"ENSG00000196954.13","gene_symbol":"CASP4","gene_name":"caspase 4 [Source:HGNC Symbol;Acc:HGNC:1505]","synonyms":"TX,ICH-2,ICE(rel)II","biotype":"protein_coding","ncbi_id":"837","summary":"This gene encodes a protein that is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain and a large and small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This caspase is able to cleave and activate its own precursor protein, as well as caspase 1 precursor. When overexpressed, this gene induces cell apoptosis. Alternative splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":104942866,"end":104969436,"strand":-1,"description":"caspase 4 [Source:HGNC Symbol;Acc:HGNC:1505]"}, {"versioned_ensembl_gene_id":"ENSG00000258503.1","gene_symbol":"AL352979.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53011971,"end":53012267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136463.7","gene_symbol":"TACO1","gene_name":"translational activator of cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:24316]","synonyms":"CCDC44","biotype":"protein_coding","ncbi_id":"51204","summary":"This gene encodes a mitochondrial protein that function as a translational activator of mitochondrially-encoded cytochrome c oxidase 1. Mutations in this gene are associated with Leigh syndrome.[provided by RefSeq, Mar 2010]","start":63600872,"end":63608365,"strand":1,"description":"translational activator of cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:24316]"}, {"versioned_ensembl_gene_id":"ENSG00000260619.1","gene_symbol":"AC068870.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80990804,"end":80993258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188152.12","gene_symbol":"NUTM2G","gene_name":"NUT family member 2G [Source:HGNC Symbol;Acc:HGNC:23449]","synonyms":"FAM22G","biotype":"protein_coding","ncbi_id":"441457","summary":null,"start":96928310,"end":96940253,"strand":1,"description":"NUT family member 2G [Source:HGNC Symbol;Acc:HGNC:23449]"}, {"versioned_ensembl_gene_id":"ENSG00000173641.17","gene_symbol":"HSPB7","gene_name":"heat shock protein family B (small) member 7 [Source:HGNC Symbol;Acc:HGNC:5249]","synonyms":"cvHSP","biotype":"protein_coding","ncbi_id":"27129","summary":"This gene encodes a small heat shock family B member that can heterodimerize with similar heat shock proteins. Defects in this gene are associated with advanced heart failure. In addition, the encoded protein may be a tumor suppressor in the p53 pathway, with defects in this gene being associated with renal cell carcinoma. [provided by RefSeq, Mar 2017]","start":16014028,"end":16019594,"strand":-1,"description":"heat shock protein family B (small) member 7 [Source:HGNC Symbol;Acc:HGNC:5249]"}, {"versioned_ensembl_gene_id":"ENSG00000232454.2","gene_symbol":"AL138752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37836044,"end":37836394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226068.1","gene_symbol":"HNRNPA3P4","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39773]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389395","summary":null,"start":48149203,"end":48150005,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39773]"}, {"versioned_ensembl_gene_id":"ENSG00000106367.13","gene_symbol":"AP1S1","gene_name":"adaptor related protein complex 1 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:559]","synonyms":"WUGSC:H_DJ0747G18.2,SIGMA1A,EKV3,CLAPS1,AP19","biotype":"protein_coding","ncbi_id":"1174","summary":"The protein encoded by this gene is part of the clathrin coat assembly complex which links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. This protein, as well as beta-prime-adaptin, gamma-adaptin, and the medium (mu) chain AP47, form the AP-1 assembly protein complex located at the Golgi vesicle. [provided by RefSeq, Jul 2008]","start":101154397,"end":101161596,"strand":1,"description":"adaptor related protein complex 1 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:559]"}, {"versioned_ensembl_gene_id":"ENSG00000128245.14","gene_symbol":"YWHAH","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta [Source:HGNC Symbol;Acc:HGNC:12853]","synonyms":"YWHA1","biotype":"protein_coding","ncbi_id":"7533","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 99% identical to the mouse, rat and bovine orthologs. This gene contains a 7 bp repeat sequence in its 5' UTR, and changes in the number of this repeat have been associated with early-onset schizophrenia and psychotic bipolar disorder. [provided by RefSeq, Jun 2009]","start":31944461,"end":31957603,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta [Source:HGNC Symbol;Acc:HGNC:12853]"}, {"versioned_ensembl_gene_id":"ENSG00000280015.1","gene_symbol":"AC024023.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":38390754,"end":38391675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128254.13","gene_symbol":"C22orf24","gene_name":"chromosome 22 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:23051]","synonyms":"HSN44A4A","biotype":"processed_transcript","ncbi_id":"25775","summary":null,"start":31933521,"end":31945518,"strand":-1,"description":"chromosome 22 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:23051]"}, {"versioned_ensembl_gene_id":"ENSG00000239839.6","gene_symbol":"DEFA3","gene_name":"defensin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2762]","synonyms":"HNP-3,DEF3","biotype":"protein_coding","ncbi_id":"1668","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. The protein encoded by this gene, defensin, alpha 3, is found in the microbicidal granules of neutrophils and likely plays a role in phagocyte-mediated host defense. Several alpha defensin genes are clustered on chromosome 8. This gene differs from defensin, alpha 1 by only one amino acid. This gene and the gene encoding defensin, alpha 1 are both subject to copy number variation. [provided by RefSeq, Oct 2014]","start":7015869,"end":7018301,"strand":-1,"description":"defensin alpha 3 [Source:HGNC Symbol;Acc:HGNC:2762]"}, {"versioned_ensembl_gene_id":"ENSG00000268583.1","gene_symbol":"AC011466.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48204083,"end":48213154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186806.5","gene_symbol":"VSIG10L","gene_name":"V-set and immunoglobulin domain containing 10 like [Source:HGNC Symbol;Acc:HGNC:27111]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147645","summary":null,"start":51331536,"end":51342124,"strand":-1,"description":"V-set and immunoglobulin domain containing 10 like [Source:HGNC Symbol;Acc:HGNC:27111]"}, {"versioned_ensembl_gene_id":"ENSG00000269892.1","gene_symbol":"AC125494.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6742985,"end":6743641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235917.1","gene_symbol":"MTCO2P11","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52027]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075214","summary":null,"start":5098341,"end":5099325,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52027]"}, {"versioned_ensembl_gene_id":"ENSG00000264813.6","gene_symbol":"AC113554.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63484823,"end":63521848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233078.1","gene_symbol":"AL355994.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16006160,"end":16006671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230496.1","gene_symbol":"MTCO2P7","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52023]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075145","summary":null,"start":130275592,"end":130276257,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52023]"}, {"versioned_ensembl_gene_id":"ENSG00000250682.5","gene_symbol":"LINC00491","gene_name":"long intergenic non-protein coding RNA 491 [Source:HGNC Symbol;Acc:HGNC:43428]","synonyms":"BC008363","biotype":"lincRNA","ncbi_id":"285708","summary":null,"start":102609156,"end":102671559,"strand":-1,"description":"long intergenic non-protein coding RNA 491 [Source:HGNC Symbol;Acc:HGNC:43428]"}, {"versioned_ensembl_gene_id":"ENSG00000228097.1","gene_symbol":"MTATP6P11","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52057]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075311","summary":null,"start":5099560,"end":5100229,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52057]"}, {"versioned_ensembl_gene_id":"ENSG00000230225.1","gene_symbol":"MTND5P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42276]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873258","summary":null,"start":5109496,"end":5110762,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42276]"}, {"versioned_ensembl_gene_id":"ENSG00000225670.4","gene_symbol":"CADM3-AS1","gene_name":"CADM3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40812]","synonyms":"CTA-134P22.2","biotype":"antisense_RNA","ncbi_id":"100131825","summary":null,"start":159194325,"end":159207973,"strand":-1,"description":"CADM3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40812]"}, {"versioned_ensembl_gene_id":"ENSG00000249997.1","gene_symbol":"MTCO3P7","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52037]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075150","summary":null,"start":130277184,"end":130277957,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52037]"}, {"versioned_ensembl_gene_id":"ENSG00000187054.15","gene_symbol":"TMPRSS11A","gene_name":"transmembrane protease, serine 11A [Source:HGNC Symbol;Acc:HGNC:27954]","synonyms":"ECRG1","biotype":"protein_coding","ncbi_id":"339967","summary":null,"start":67909385,"end":67964140,"strand":-1,"description":"transmembrane protease, serine 11A [Source:HGNC Symbol;Acc:HGNC:27954]"}, {"versioned_ensembl_gene_id":"ENSG00000232990.2","gene_symbol":"MTATP6P7","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44581]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480798","summary":null,"start":130276507,"end":130277187,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44581]"}, {"versioned_ensembl_gene_id":"ENSG00000236254.1","gene_symbol":"MTND4P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42201]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100653489","summary":null,"start":5107937,"end":5109290,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42201]"}, {"versioned_ensembl_gene_id":"ENSG00000282051.1","gene_symbol":"AC010507.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":197961,"end":200775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247402.2","gene_symbol":"AC099487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102605635,"end":102606197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177410.12","gene_symbol":"ZFAS1","gene_name":"ZNFX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33101]","synonyms":"ZNFX1-AS1,NCRNA00275,HSUP2,HSUP1,C20orf199","biotype":"antisense_RNA","ncbi_id":"441951","summary":"This gene represents a snoRNA host gene that produces a non-coding RNA. Increased expression or amplification of this locus is associated with cancer progression and metastasis. This transcript regulates expression of genes involved in differentiation. It may act a molecular sponge for microRNAs. Alternatively spliced transcript variants have been observed. [provided by RefSeq, Dec 2017]","start":49278178,"end":49295738,"strand":1,"description":"ZNFX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:33101]"}, {"versioned_ensembl_gene_id":"ENSG00000248136.1","gene_symbol":"MTND6P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39471]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480726","summary":null,"start":130282085,"end":130282606,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39471]"}, {"versioned_ensembl_gene_id":"ENSG00000279829.1","gene_symbol":"AC015959.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46385707,"end":46387083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261385.1","gene_symbol":"AC009088.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31131433,"end":31131877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233460.1","gene_symbol":"RPL35AP31","gene_name":"ribosomal protein L35a pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:36284]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271640","summary":null,"start":71845981,"end":71846317,"strand":1,"description":"ribosomal protein L35a pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:36284]"}, {"versioned_ensembl_gene_id":"ENSG00000096968.13","gene_symbol":"JAK2","gene_name":"Janus kinase 2 [Source:HGNC Symbol;Acc:HGNC:6192]","synonyms":"JTK10","biotype":"protein_coding","ncbi_id":"3717","summary":"This gene encodes a non-receptor tyrosine kinase that plays a central role in cytokine and growth factor signalling. The primary isoform of this protein has an N-terminal FERM domain that is required for erythropoietin receptor association, an SH2 domain that binds STAT transcription factors, a pseudokinase domain and a C-terminal tyrosine kinase domain. Cytokine binding induces autophosphorylation and activation of this kinase. This kinase then recruits and phosphorylates signal transducer and activator of transcription (STAT) proteins. Growth factors like TGF-beta 1 also induce phosphorylation and activation of this kinase and translocation of downstream STAT proteins to the nucleus where they influence gene transcription. Mutations in this gene are associated with numerous inflammatory diseases and malignancies. This gene is a downstream target of the pleiotropic cytokine IL6 that is produced by B cells, T cells, dendritic cells and macrophages to produce an immune response or inflammation. Disregulation of the IL6/JAK2/STAT3 signalling pathways produces increased cellular proliferation and myeloproliferative neoplasms of hematopoietic stem cells. A nonsynonymous mutation in the pseudokinase domain of this gene disrupts the domains inhibitory effect and results in constitutive tyrosine phosphorylation activity and hypersensitivity to cytokine signalling. This gene and the IL6/JAK2/STAT3 signalling pathway is a therapeutic target for the treatment of excessive inflammatory responses to viral infections. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2020]","start":4984390,"end":5128183,"strand":1,"description":"Janus kinase 2 [Source:HGNC Symbol;Acc:HGNC:6192]"}, {"versioned_ensembl_gene_id":"ENSG00000168528.11","gene_symbol":"SERINC2","gene_name":"serine incorporator 2 [Source:HGNC Symbol;Acc:HGNC:23231]","synonyms":"TDE2L,TDE2,PRO0899,FKSG84","biotype":"protein_coding","ncbi_id":"347735","summary":null,"start":31409565,"end":31434680,"strand":1,"description":"serine incorporator 2 [Source:HGNC Symbol;Acc:HGNC:23231]"}, {"versioned_ensembl_gene_id":"ENSG00000250958.1","gene_symbol":"LINC00492","gene_name":"long intergenic non-protein coding RNA 492 [Source:HGNC Symbol;Acc:HGNC:43429]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861468","summary":null,"start":102581368,"end":102617589,"strand":1,"description":"long intergenic non-protein coding RNA 492 [Source:HGNC Symbol;Acc:HGNC:43429]"}, {"versioned_ensembl_gene_id":"ENSG00000282508.1","gene_symbol":"LINC01002","gene_name":"long intergenic non-protein coding RNA 1002 [Source:HGNC Symbol;Acc:HGNC:38538]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"399844","summary":null,"start":198264,"end":239440,"strand":-1,"description":"long intergenic non-protein coding RNA 1002 [Source:HGNC Symbol;Acc:HGNC:38538]"}, {"versioned_ensembl_gene_id":"ENSG00000257354.2","gene_symbol":"AC048341.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62602752,"end":62622213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181939.3","gene_symbol":"OR4C15","gene_name":"olfactory receptor family 4 subfamily C member 15 [Source:HGNC Symbol;Acc:HGNC:15171]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81309","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55554307,"end":55555419,"strand":1,"description":"olfactory receptor family 4 subfamily C member 15 [Source:HGNC Symbol;Acc:HGNC:15171]"}, {"versioned_ensembl_gene_id":"ENSG00000169551.12","gene_symbol":"CT55","gene_name":"cancer/testis antigen 55 [Source:HGNC Symbol;Acc:HGNC:26047]","synonyms":"FLJ20527,CXorf48","biotype":"protein_coding","ncbi_id":"54967","summary":null,"start":135156536,"end":135171398,"strand":-1,"description":"cancer/testis antigen 55 [Source:HGNC Symbol;Acc:HGNC:26047]"}, {"versioned_ensembl_gene_id":"ENSG00000221949.5","gene_symbol":"LINC01465","gene_name":"long intergenic non-protein coding RNA 1465 [Source:HGNC Symbol;Acc:HGNC:26364]","synonyms":"FLJ25590,C12orf61","biotype":"lincRNA","ncbi_id":"283416","summary":null,"start":62601751,"end":62603690,"strand":-1,"description":"long intergenic non-protein coding RNA 1465 [Source:HGNC Symbol;Acc:HGNC:26364]"}, {"versioned_ensembl_gene_id":"ENSG00000243824.1","gene_symbol":"RPL12P6","gene_name":"ribosomal protein L12 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23538]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440176","summary":null,"start":34740336,"end":34740833,"strand":-1,"description":"ribosomal protein L12 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23538]"}, {"versioned_ensembl_gene_id":"ENSG00000279514.2","gene_symbol":"OR4C16","gene_name":"olfactory receptor family 4 subfamily C member 16 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15172]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"219428","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":55572128,"end":55573060,"strand":1,"description":"olfactory receptor family 4 subfamily C member 16 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15172]"}, {"versioned_ensembl_gene_id":"ENSG00000275180.1","gene_symbol":"AC048341.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62603909,"end":62604399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238031.1","gene_symbol":"AC090505.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194827890,"end":194832592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283529.1","gene_symbol":"AL035685.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49318337,"end":49441654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283940.1","gene_symbol":"AC068137.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130278036,"end":130278376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172188.5","gene_symbol":"OR4C11","gene_name":"olfactory receptor family 4 subfamily C member 11 [Source:HGNC Symbol;Acc:HGNC:15167]","synonyms":"OR4C11P","biotype":"protein_coding","ncbi_id":"219429","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55602360,"end":55607645,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 11 [Source:HGNC Symbol;Acc:HGNC:15167]"}, {"versioned_ensembl_gene_id":"ENSG00000198732.10","gene_symbol":"SMOC1","gene_name":"SPARC related modular calcium binding 1 [Source:HGNC Symbol;Acc:HGNC:20318]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64093","summary":"This gene encodes a multi-domain secreted protein that may have a critical role in ocular and limb development. Mutations in this gene are associated with microphthalmia and limb anomalies. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":69854131,"end":70032366,"strand":1,"description":"SPARC related modular calcium binding 1 [Source:HGNC Symbol;Acc:HGNC:20318]"}, {"versioned_ensembl_gene_id":"ENSG00000284171.1","gene_symbol":"AC068137.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130278444,"end":130278739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230548.1","gene_symbol":"MTND4P27","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42214]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873248","summary":null,"start":130278757,"end":130280110,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42214]"}, {"versioned_ensembl_gene_id":"ENSG00000181927.3","gene_symbol":"OR4P4","gene_name":"olfactory receptor family 4 subfamily P member 4 [Source:HGNC Symbol;Acc:HGNC:15180]","synonyms":"OR4P3P","biotype":"protein_coding","ncbi_id":"81300","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55635113,"end":55640309,"strand":1,"description":"olfactory receptor family 4 subfamily P member 4 [Source:HGNC Symbol;Acc:HGNC:15180]"}, {"versioned_ensembl_gene_id":"ENSG00000234934.1","gene_symbol":"MTND5P29","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42291]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873265","summary":null,"start":130280299,"end":130282105,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42291]"}, {"versioned_ensembl_gene_id":"ENSG00000233550.1","gene_symbol":"MTCYBP8","gene_name":"mitochondrially encoded cytochrome b pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075220","summary":null,"start":130282679,"end":130283329,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51965]"}, {"versioned_ensembl_gene_id":"ENSG00000232733.3","gene_symbol":"RPL12P1","gene_name":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]","synonyms":"RPL12-L,dJ570F3.5,CICK0721Q.1","biotype":"processed_pseudogene","ncbi_id":"729727","summary":null,"start":33540223,"end":33540720,"strand":-1,"description":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]"}, {"versioned_ensembl_gene_id":"ENSG00000277142.1","gene_symbol":"Z98882.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":525155,"end":527407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174982.3","gene_symbol":"OR4S2","gene_name":"olfactory receptor family 4 subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:15183]","synonyms":"OST725,OR4S2P","biotype":"protein_coding","ncbi_id":"219431","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55648327,"end":55652854,"strand":1,"description":"olfactory receptor family 4 subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:15183]"}, {"versioned_ensembl_gene_id":"ENSG00000213287.3","gene_symbol":"AP001102.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87258851,"end":87259259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279836.1","gene_symbol":"AP002967.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87121058,"end":87121596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236491.1","gene_symbol":"AC234771.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135180255,"end":135194679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228922.1","gene_symbol":"AC234771.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":135201731,"end":135215232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240247.7","gene_symbol":"DEFA1B","gene_name":"defensin alpha 1B [Source:HGNC Symbol;Acc:HGNC:33596]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728358","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. The protein encoded by this gene, defensin, alpha 1, is found in the microbicidal granules of neutrophils and likely plays a role in phagocyte-mediated host defense. Several alpha defensin genes are clustered on chromosome 8. This gene differs from defensin, alpha 3 by only one amino acid. This gene and the gene encoding defensin, alpha 3 are both subject to copy number variation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":6996766,"end":6999195,"strand":-1,"description":"defensin alpha 1B [Source:HGNC Symbol;Acc:HGNC:33596]"}, {"versioned_ensembl_gene_id":"ENSG00000204186.7","gene_symbol":"ZDBF2","gene_name":"zinc finger DBF-type containing 2 [Source:HGNC Symbol;Acc:HGNC:29313]","synonyms":"Slx9,KIAA1571,FLJ45338","biotype":"protein_coding","ncbi_id":"57683","summary":"This gene encodes a protein containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":206274663,"end":206314428,"strand":1,"description":"zinc finger DBF-type containing 2 [Source:HGNC Symbol;Acc:HGNC:29313]"}, {"versioned_ensembl_gene_id":"ENSG00000181903.5","gene_symbol":"OR4C6","gene_name":"olfactory receptor family 4 subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:14743]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219432","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55662201,"end":55666195,"strand":1,"description":"olfactory receptor family 4 subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:14743]"}, {"versioned_ensembl_gene_id":"ENSG00000268220.1","gene_symbol":"AC008040.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170087810,"end":170089590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224923.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"AB023051.1,NCRNA00149","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30757206,"end":30782937,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000166575.16","gene_symbol":"TMEM135","gene_name":"transmembrane protein 135 [Source:HGNC Symbol;Acc:HGNC:26167]","synonyms":"FLJ22104","biotype":"protein_coding","ncbi_id":"65084","summary":null,"start":87037844,"end":87323758,"strand":1,"description":"transmembrane protein 135 [Source:HGNC Symbol;Acc:HGNC:26167]"}, {"versioned_ensembl_gene_id":"ENSG00000254841.1","gene_symbol":"OR4V1P","gene_name":"olfactory receptor family 4 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14736]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79534","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55673536,"end":55674675,"strand":1,"description":"olfactory receptor family 4 subfamily V member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14736]"}, {"versioned_ensembl_gene_id":"ENSG00000173889.15","gene_symbol":"PHC3","gene_name":"polyhomeotic homolog 3 [Source:HGNC Symbol;Acc:HGNC:15682]","synonyms":"FLJ12967,FLJ12729,EDR3,HPH3","biotype":"protein_coding","ncbi_id":"80012","summary":null,"start":170086732,"end":170181749,"strand":-1,"description":"polyhomeotic homolog 3 [Source:HGNC Symbol;Acc:HGNC:15682]"}, {"versioned_ensembl_gene_id":"ENSG00000112232.8","gene_symbol":"KHDRBS2","gene_name":"KH RNA binding domain containing, signal transduction associated 2 [Source:HGNC Symbol;Acc:HGNC:18114]","synonyms":"SLM1,SLM-1,MGC26664","biotype":"protein_coding","ncbi_id":"202559","summary":null,"start":61679960,"end":62286227,"strand":-1,"description":"KH RNA binding domain containing, signal transduction associated 2 [Source:HGNC Symbol;Acc:HGNC:18114]"}, {"versioned_ensembl_gene_id":"ENSG00000109163.6","gene_symbol":"GNRHR","gene_name":"gonadotropin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4421]","synonyms":"LHRHR,GRHR","biotype":"protein_coding","ncbi_id":"2798","summary":"This gene encodes the receptor for type 1 gonadotropin-releasing hormone. This receptor is a member of the seven-transmembrane, G-protein coupled receptor (GPCR) family. It is expressed on the surface of pituitary gonadotrope cells as well as lymphocytes, breast, ovary, and prostate. Following binding of gonadotropin-releasing hormone, the receptor associates with G-proteins that activate a phosphatidylinositol-calcium second messenger system. Activation of the receptor ultimately causes the release of gonadotropic luteinizing hormone (LH) and follicle stimulating hormone (FSH). Defects in this gene are a cause of hypogonadotropic hypogonadism (HH). Alternative splicing results in multiple transcript variants encoding different isoforms. More than 18 transcription initiation sites in the 5' region and multiple polyA signals in the 3' region have been identified for this gene. [provided by RefSeq, Jul 2008]","start":67739328,"end":67754360,"strand":-1,"description":"gonadotropin releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4421]"}, {"versioned_ensembl_gene_id":"ENSG00000255916.1","gene_symbol":"AC148477.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132329850,"end":132331575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206486.8","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DBP2,Prp2,DDX16,PRPF2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30642608,"end":30662557,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000269833.2","gene_symbol":"AC234771.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135236895,"end":135237408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227596.5","gene_symbol":"CR388215.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30789330,"end":30821330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180105.11","gene_symbol":"AC017081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206410087,"end":206410909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219940.2","gene_symbol":"SPTLC1P3","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39670]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874499","summary":null,"start":63227485,"end":63227743,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39670]"}, {"versioned_ensembl_gene_id":"ENSG00000251220.2","gene_symbol":"RFPL4AP3","gene_name":"ret finger protein like 4A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480810","summary":null,"start":23514940,"end":23515284,"strand":-1,"description":"ret finger protein like 4A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45139]"}, {"versioned_ensembl_gene_id":"ENSG00000249645.1","gene_symbol":"AC114912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23105502,"end":23123487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103381.11","gene_symbol":"CPPED1","gene_name":"calcineurin like phosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25632]","synonyms":"FLJ11151,CSTP1","biotype":"protein_coding","ncbi_id":"55313","summary":null,"start":12659799,"end":12804017,"strand":-1,"description":"calcineurin like phosphoesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25632]"}, {"versioned_ensembl_gene_id":"ENSG00000184436.11","gene_symbol":"THAP7","gene_name":"THAP domain containing 7 [Source:HGNC Symbol;Acc:HGNC:23190]","synonyms":"MGC10963","biotype":"protein_coding","ncbi_id":"80764","summary":null,"start":20999104,"end":21002196,"strand":-1,"description":"THAP domain containing 7 [Source:HGNC Symbol;Acc:HGNC:23190]"}, {"versioned_ensembl_gene_id":"ENSG00000232701.1","gene_symbol":"RPL21P108","gene_name":"ribosomal protein L21 pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:35496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271434","summary":null,"start":74377163,"end":74377951,"strand":-1,"description":"ribosomal protein L21 pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:35496]"}, {"versioned_ensembl_gene_id":"ENSG00000215899.3","gene_symbol":"AC209007.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31487589,"end":31488930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067167.7","gene_symbol":"TRAM1","gene_name":"translocation associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:20568]","synonyms":"TRAMP,TRAM","biotype":"protein_coding","ncbi_id":"23471","summary":"This gene encodes a multi-pass membrane protein that is part of the mammalian endoplasmic reticulum. The encoded protein influences glycosylation and facilitates the translocation of secretory proteins across the endoplasmic reticulum membrane by regulating which domains of the nascent polypeptide chain are visible to the cytosol during a translocational pause. [provided by RefSeq, Oct 2009]","start":70573442,"end":70608387,"strand":-1,"description":"translocation associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:20568]"}, {"versioned_ensembl_gene_id":"ENSG00000162068.1","gene_symbol":"NTN3","gene_name":"netrin 3 [Source:HGNC Symbol;Acc:HGNC:8030]","synonyms":"NTN2L","biotype":"protein_coding","ncbi_id":"4917","summary":null,"start":2471499,"end":2474145,"strand":1,"description":"netrin 3 [Source:HGNC Symbol;Acc:HGNC:8030]"}, {"versioned_ensembl_gene_id":"ENSG00000253716.5","gene_symbol":"MINCR","gene_name":"MYC-induced long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51653]","synonyms":"TCONS_00015189,LINC01604","biotype":"antisense_RNA","ncbi_id":"100507316","summary":null,"start":143280161,"end":143281690,"strand":-1,"description":"MYC-induced long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51653]"}, {"versioned_ensembl_gene_id":"ENSG00000135404.11","gene_symbol":"CD63","gene_name":"CD63 molecule [Source:HGNC Symbol;Acc:HGNC:1692]","synonyms":"TSPAN30,MLA1,ME491","biotype":"protein_coding","ncbi_id":"967","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. The encoded protein is a cell surface glycoprotein that is known to complex with integrins. It may function as a blood platelet activation marker. Deficiency of this protein is associated with Hermansky-Pudlak syndrome. Also this gene has been associated with tumor progression. Alternative splicing results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Apr 2012]","start":55725323,"end":55729707,"strand":-1,"description":"CD63 molecule [Source:HGNC Symbol;Acc:HGNC:1692]"}, {"versioned_ensembl_gene_id":"ENSG00000165359.15","gene_symbol":"INTS6L","gene_name":"integrator complex subunit 6 like [Source:HGNC Symbol;Acc:HGNC:27334]","synonyms":"FLJ41215,DDX26B","biotype":"protein_coding","ncbi_id":"203522","summary":null,"start":135520643,"end":135582510,"strand":1,"description":"integrator complex subunit 6 like [Source:HGNC Symbol;Acc:HGNC:27334]"}, {"versioned_ensembl_gene_id":"ENSG00000248227.1","gene_symbol":"LINC02513","gene_name":"long intergenic non-protein coding RNA 2513 [Source:HGNC Symbol;Acc:HGNC:53502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374410","summary":null,"start":38366914,"end":38385759,"strand":1,"description":"long intergenic non-protein coding RNA 2513 [Source:HGNC Symbol;Acc:HGNC:53502]"}, {"versioned_ensembl_gene_id":"ENSG00000230080.2","gene_symbol":"AC139143.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1802889,"end":1804095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264108.1","gene_symbol":"AC090457.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76008118,"end":76015861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279700.1","gene_symbol":"AC131212.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132565071,"end":132566425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232458.1","gene_symbol":"LINC01450","gene_name":"long intergenic non-protein coding RNA 1450 [Source:HGNC Symbol;Acc:HGNC:50792]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928744","summary":null,"start":40964667,"end":40979939,"strand":-1,"description":"long intergenic non-protein coding RNA 1450 [Source:HGNC Symbol;Acc:HGNC:50792]"}, {"versioned_ensembl_gene_id":"ENSG00000124784.8","gene_symbol":"RIOK1","gene_name":"RIO kinase 1 [Source:HGNC Symbol;Acc:HGNC:18656]","synonyms":"AD034,RRP10,FLJ30006,bA288G3.1","biotype":"protein_coding","ncbi_id":"83732","summary":"The protein encoded by this gene competes with pICln for inclusion in the protein arginine methyltransferase 5 complex. This complex targets substrates for dimethylation. The encoded protein is essential for the last steps in the maturation of 40S subunits. [provided by RefSeq, Jan 2017]","start":7389496,"end":7418037,"strand":1,"description":"RIO kinase 1 [Source:HGNC Symbol;Acc:HGNC:18656]"}, {"versioned_ensembl_gene_id":"ENSG00000129521.13","gene_symbol":"EGLN3","gene_name":"egl-9 family hypoxia inducible factor 3 [Source:HGNC Symbol;Acc:HGNC:14661]","synonyms":"PHD3,HIFPH3","biotype":"protein_coding","ncbi_id":"112399","summary":null,"start":33924231,"end":34462774,"strand":-1,"description":"egl-9 family hypoxia inducible factor 3 [Source:HGNC Symbol;Acc:HGNC:14661]"}, {"versioned_ensembl_gene_id":"ENSG00000186376.14","gene_symbol":"ZNF75D","gene_name":"zinc finger protein 75D [Source:HGNC Symbol;Acc:HGNC:13145]","synonyms":"ZNF75,ZKSCAN24,D8C6,ZSCAN28,ZNF82","biotype":"protein_coding","ncbi_id":"7626","summary":"This gene encodes a protein that likely functions as a transcription factor. The protein, which belongs to the ZNF75 family, includes an N-terminal SCAN domain, a KRAB box, and five C2H2-type zinc finger motifs. Another functional gene belonging to this family is located on chromosome 16, while pseudogenes have been identified on chromosomes 11 and 12. Alternative splicing results in multiple transcripts variants. [provided by RefSeq, Jun 2010]","start":135248920,"end":135344087,"strand":-1,"description":"zinc finger protein 75D [Source:HGNC Symbol;Acc:HGNC:13145]"}, {"versioned_ensembl_gene_id":"ENSG00000215805.3","gene_symbol":"AL356361.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":239972787,"end":239974245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270228.1","gene_symbol":"AC079880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67718996,"end":67724262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169871.12","gene_symbol":"TRIM56","gene_name":"tripartite motif containing 56 [Source:HGNC Symbol;Acc:HGNC:19028]","synonyms":"RNF109","biotype":"protein_coding","ncbi_id":"81844","summary":null,"start":101085439,"end":101097967,"strand":1,"description":"tripartite motif containing 56 [Source:HGNC Symbol;Acc:HGNC:19028]"}, {"versioned_ensembl_gene_id":"ENSG00000283392.1","gene_symbol":"AC090952.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14602035,"end":14641443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215369.3","gene_symbol":"RPL37P3","gene_name":"ribosomal protein L37 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:17238]","synonyms":"RL37P","biotype":"processed_pseudogene","ncbi_id":"378818","summary":null,"start":17894193,"end":17894485,"strand":-1,"description":"ribosomal protein L37 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:17238]"}, {"versioned_ensembl_gene_id":"ENSG00000105383.14","gene_symbol":"CD33","gene_name":"CD33 molecule [Source:HGNC Symbol;Acc:HGNC:1659]","synonyms":"SIGLEC-3,p67,FLJ00391,SIGLEC3","biotype":"protein_coding","ncbi_id":"945","summary":null,"start":51225064,"end":51243860,"strand":1,"description":"CD33 molecule [Source:HGNC Symbol;Acc:HGNC:1659]"}, {"versioned_ensembl_gene_id":"ENSG00000254837.2","gene_symbol":"AP001372.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":74493366,"end":74498533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216917.2","gene_symbol":"AC005587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131780721,"end":131781312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259438.1","gene_symbol":"AC090970.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52010999,"end":52019095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271264.1","gene_symbol":"MZT1P1","gene_name":"mitotic spindle organizing protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50605]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480302","summary":null,"start":9780822,"end":9781240,"strand":1,"description":"mitotic spindle organizing protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50605]"}, {"versioned_ensembl_gene_id":"ENSG00000268849.5","gene_symbol":"SIGLEC22P","gene_name":"sialic acid binding Ig like lectin 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:15611]","synonyms":"SIGLECP6","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"114195","summary":null,"start":51211080,"end":51212088,"strand":1,"description":"sialic acid binding Ig like lectin 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:15611]"}, {"versioned_ensembl_gene_id":"ENSG00000269253.1","gene_symbol":"SIGLEC21P","gene_name":"sialic acid binding Ig like lectin 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:15610]","synonyms":"SIGLECP5","biotype":"unprocessed_pseudogene","ncbi_id":"114194","summary":null,"start":51198855,"end":51201449,"strand":1,"description":"sialic acid binding Ig like lectin 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:15610]"}, {"versioned_ensembl_gene_id":"ENSG00000154165.4","gene_symbol":"GPR15","gene_name":"G protein-coupled receptor 15 [Source:HGNC Symbol;Acc:HGNC:4469]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2838","summary":"This gene encodes a G protein-coupled receptor that acts as a chemokine receptor for human immunodeficiency virus type 1 and 2. The encoded protein localizes to the cell membrane. [provided by RefSeq, Nov 2012]","start":98531899,"end":98533150,"strand":1,"description":"G protein-coupled receptor 15 [Source:HGNC Symbol;Acc:HGNC:4469]"}, {"versioned_ensembl_gene_id":"ENSG00000138594.13","gene_symbol":"TMOD3","gene_name":"tropomodulin 3 [Source:HGNC Symbol;Acc:HGNC:11873]","synonyms":"UTMOD","biotype":"protein_coding","ncbi_id":"29766","summary":null,"start":51829628,"end":51947295,"strand":1,"description":"tropomodulin 3 [Source:HGNC Symbol;Acc:HGNC:11873]"}, {"versioned_ensembl_gene_id":"ENSG00000091129.19","gene_symbol":"NRCAM","gene_name":"neuronal cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:7994]","synonyms":"KIAA0343,Bravo","biotype":"protein_coding","ncbi_id":"4897","summary":"Cell adhesion molecules (CAMs) are members of the immunoglobulin superfamily. This gene encodes a neuronal cell adhesion molecule with multiple immunoglobulin-like C2-type domains and fibronectin type-III domains. This ankyrin-binding protein is involved in neuron-neuron adhesion and promotes directional signaling during axonal cone growth. This gene is also expressed in non-neural tissues and may play a general role in cell-cell communication via signaling from its intracellular domain to the actin cytoskeleton during directional cell migration. Allelic variants of this gene have been associated with autism and addiction vulnerability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":108147623,"end":108456717,"strand":-1,"description":"neuronal cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:7994]"}, {"versioned_ensembl_gene_id":"ENSG00000271427.1","gene_symbol":"AL358072.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117364899,"end":117365473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279039.1","gene_symbol":"AC011447.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20207192,"end":20209789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107758.15","gene_symbol":"PPP3CB","gene_name":"protein phosphatase 3 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9315]","synonyms":"PP2Bbeta,CNA2,CALNB,CALNA2","biotype":"protein_coding","ncbi_id":"5532","summary":null,"start":73436428,"end":73496024,"strand":-1,"description":"protein phosphatase 3 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9315]"}, {"versioned_ensembl_gene_id":"ENSG00000223982.3","gene_symbol":"SNRPD2P2","gene_name":"small nuclear ribonucleoprotein D2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645339","summary":null,"start":231475956,"end":231476288,"strand":-1,"description":"small nuclear ribonucleoprotein D2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38598]"}, {"versioned_ensembl_gene_id":"ENSG00000063761.15","gene_symbol":"ADCK1","gene_name":"aarF domain containing kinase 1 [Source:HGNC Symbol;Acc:HGNC:19038]","synonyms":"FLJ39600","biotype":"protein_coding","ncbi_id":"57143","summary":null,"start":77800083,"end":77935012,"strand":1,"description":"aarF domain containing kinase 1 [Source:HGNC Symbol;Acc:HGNC:19038]"}, {"versioned_ensembl_gene_id":"ENSG00000171916.16","gene_symbol":"LGALS9C","gene_name":"galectin 9C [Source:HGNC Symbol;Acc:HGNC:33874]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654346","summary":"This gene was initially thought to represent a pseudogene of galectin 9; however, this transcript has good exon-intron structure and encodes a predicted protein of the same size as and highly similar to galectin 9. This gene is one of two similar loci on chromosome 17p similar to galectin 9 and now thought to be protein-encoding. This gene is the more telomeric gene. [provided by RefSeq, Jul 2008]","start":18476737,"end":18494945,"strand":1,"description":"galectin 9C [Source:HGNC Symbol;Acc:HGNC:33874]"}, {"versioned_ensembl_gene_id":"ENSG00000271010.1","gene_symbol":"AC011475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10598001,"end":10598965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274033.1","gene_symbol":"AC006539.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20056466,"end":20056594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255256.1","gene_symbol":"AL136146.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35972428,"end":35989007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235333.3","gene_symbol":"PVRIG2P","gene_name":"poliovirus receptor related immunoglobulin domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:48897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101752334","summary":null,"start":100352360,"end":100353692,"strand":1,"description":"poliovirus receptor related immunoglobulin domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:48897]"}, {"versioned_ensembl_gene_id":"ENSG00000247982.6","gene_symbol":"LINC00926","gene_name":"long intergenic non-protein coding RNA 926 [Source:HGNC Symbol;Acc:HGNC:27514]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283663","summary":null,"start":57300365,"end":57307769,"strand":1,"description":"long intergenic non-protein coding RNA 926 [Source:HGNC Symbol;Acc:HGNC:27514]"}, {"versioned_ensembl_gene_id":"ENSG00000168992.4","gene_symbol":"OR7E102P","gene_name":"olfactory receptor family 7 subfamily E member 102 pseudogene [Source:HGNC Symbol;Acc:HGNC:15043]","synonyms":"OR7E102","biotype":"unprocessed_pseudogene","ncbi_id":"400984","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":95546531,"end":95547545,"strand":1,"description":"olfactory receptor family 7 subfamily E member 102 pseudogene [Source:HGNC Symbol;Acc:HGNC:15043]"}, {"versioned_ensembl_gene_id":"ENSG00000126266.3","gene_symbol":"FFAR1","gene_name":"free fatty acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:4498]","synonyms":"GPR40,FFA1R","biotype":"protein_coding","ncbi_id":"2864","summary":"This gene encodes a member of the GP40 family of G protein-coupled receptors that are clustered together on chromosome 19. The encoded protein is a receptor for medium and long chain free fatty acids and may be involved in the metabolic regulation of insulin secretion. Polymorphisms in this gene may be associated with type 2 diabetes. [provided by RefSeq, Apr 2009]","start":35351552,"end":35353862,"strand":1,"description":"free fatty acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:4498]"}, {"versioned_ensembl_gene_id":"ENSG00000224107.5","gene_symbol":"ETDB","gene_name":"embryonic testis differentiation homolog B [Source:HGNC Symbol;Acc:HGNC:44269]","synonyms":"LINC00633","biotype":"protein_coding","ncbi_id":"100129515","summary":null,"start":135118955,"end":135120526,"strand":-1,"description":"embryonic testis differentiation homolog B [Source:HGNC Symbol;Acc:HGNC:44269]"}, {"versioned_ensembl_gene_id":"ENSG00000253173.3","gene_symbol":"AC084251.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70103798,"end":70104179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157150.4","gene_symbol":"TIMP4","gene_name":"TIMP metallopeptidase inhibitor 4 [Source:HGNC Symbol;Acc:HGNC:11823]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7079","summary":"This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. The secreted, netrin domain-containing protein encoded by this gene is involved in regulation of platelet aggregation and recruitment and may play role in hormonal regulation and endometrial tissue remodeling. [provided by RefSeq, Jul 2008]","start":12153051,"end":12159351,"strand":-1,"description":"TIMP metallopeptidase inhibitor 4 [Source:HGNC Symbol;Acc:HGNC:11823]"}, {"versioned_ensembl_gene_id":"ENSG00000279933.1","gene_symbol":"AL031595.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44183031,"end":44187739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226642.1","gene_symbol":"ACTG1P12","gene_name":"actin gamma 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418921","summary":null,"start":12070195,"end":12071360,"strand":1,"description":"actin gamma 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:44496]"}, {"versioned_ensembl_gene_id":"ENSG00000273305.1","gene_symbol":"AC009237.15","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95537969,"end":95538469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157152.16","gene_symbol":"SYN2","gene_name":"synapsin II [Source:HGNC Symbol;Acc:HGNC:11495]","synonyms":"SYNIIb,SYNIIa,SYNII","biotype":"protein_coding","ncbi_id":"6854","summary":"This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014]","start":12004402,"end":12191400,"strand":1,"description":"synapsin II [Source:HGNC Symbol;Acc:HGNC:11495]"}, {"versioned_ensembl_gene_id":"ENSG00000212961.4","gene_symbol":"HNRNPA1P40","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:48769]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129920","summary":null,"start":74354443,"end":74355720,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:48769]"}, {"versioned_ensembl_gene_id":"ENSG00000214787.9","gene_symbol":"MS4A4E","gene_name":"membrane spanning 4-domains A4E [Source:HGNC Symbol;Acc:HGNC:14284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643680","summary":"Most MS4A genes, including MS4A4E, encode proteins with at least 4 potential transmembrane domains and N- and C-terminal cytoplasmic domains encoded by distinct exons.[supplied by OMIM, Apr 2004]","start":60201253,"end":60243088,"strand":-1,"description":"membrane spanning 4-domains A4E [Source:HGNC Symbol;Acc:HGNC:14284]"}, {"versioned_ensembl_gene_id":"ENSG00000236303.2","gene_symbol":"AL355500.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130439067,"end":130483154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280393.1","gene_symbol":"AC090574.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69938168,"end":69938400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279464.1","gene_symbol":"AC096720.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67607856,"end":67610313,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225604.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859634,"end":28863359,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000226575.3","gene_symbol":"MYL8P","gene_name":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]","synonyms":"BING3","biotype":"processed_pseudogene","ncbi_id":"442204","summary":null,"start":33260584,"end":33261101,"strand":1,"description":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]"}, {"versioned_ensembl_gene_id":"ENSG00000158373.8","gene_symbol":"HIST1H2BD","gene_name":"histone cluster 1 H2B family member d [Source:HGNC Symbol;Acc:HGNC:4747]","synonyms":"H2BFB,H2B/b","biotype":"protein_coding","ncbi_id":"3017","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Two transcripts that encode the same protein have been identified for this gene, which is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26158146,"end":26171349,"strand":1,"description":"histone cluster 1 H2B family member d [Source:HGNC Symbol;Acc:HGNC:4747]"}, {"versioned_ensembl_gene_id":"ENSG00000216331.2","gene_symbol":"HIST1H1PS1","gene_name":"histone cluster 1 H1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19163]","synonyms":"H1F6P,FLJ39701,dJ34B20.16","biotype":"unprocessed_pseudogene","ncbi_id":"387325","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This histone pseudogene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Oct 2015]","start":26195554,"end":26196633,"strand":1,"description":"histone cluster 1 H1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19163]"}, {"versioned_ensembl_gene_id":"ENSG00000148498.15","gene_symbol":"PARD3","gene_name":"par-3 family cell polarity regulator [Source:HGNC Symbol;Acc:HGNC:16051]","synonyms":"PPP1R118,PARD3A,PAR3,Bazooka,Baz,ASIP","biotype":"protein_coding","ncbi_id":"56288","summary":"This gene encodes a member of the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]","start":34109560,"end":34815325,"strand":-1,"description":"par-3 family cell polarity regulator [Source:HGNC Symbol;Acc:HGNC:16051]"}, {"versioned_ensembl_gene_id":"ENSG00000234167.1","gene_symbol":"ELOBP4","gene_name":"elongin B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39722]","synonyms":"TCEB2P4","biotype":"processed_pseudogene","ncbi_id":"100874519","summary":null,"start":34488583,"end":34488878,"strand":-1,"description":"elongin B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39722]"}, {"versioned_ensembl_gene_id":"ENSG00000271936.1","gene_symbol":"AC012073.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24825610,"end":24826717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264513.1","gene_symbol":"AC006270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63117019,"end":63130947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277218.1","gene_symbol":"AL139123.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":130104569,"end":130104998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237489.3","gene_symbol":"LINC00959","gene_name":"long intergenic non-protein coding RNA 959 [Source:HGNC Symbol;Acc:HGNC:48677]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387723","summary":null,"start":130063900,"end":130110817,"strand":-1,"description":"long intergenic non-protein coding RNA 959 [Source:HGNC Symbol;Acc:HGNC:48677]"}, {"versioned_ensembl_gene_id":"ENSG00000265000.1","gene_symbol":"AC068512.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62808500,"end":62836371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280091.1","gene_symbol":"AC020895.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6894994,"end":6896832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100412.15","gene_symbol":"ACO2","gene_name":"aconitase 2 [Source:HGNC Symbol;Acc:HGNC:118]","synonyms":"ACONM","biotype":"protein_coding","ncbi_id":"50","summary":"The protein encoded by this gene belongs to the aconitase/IPM isomerase family. It is an enzyme that catalyzes the interconversion of citrate to isocitrate via cis-aconitate in the second step of the TCA cycle. This protein is encoded in the nucleus and functions in the mitochondrion. It was found to be one of the mitochondrial matrix proteins that are preferentially degraded by the serine protease 15(PRSS15), also known as Lon protease, after oxidative modification. [provided by RefSeq, Jul 2008]","start":41469125,"end":41528989,"strand":1,"description":"aconitase 2 [Source:HGNC Symbol;Acc:HGNC:118]"}, {"versioned_ensembl_gene_id":"ENSG00000233752.1","gene_symbol":"AC009414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36299388,"end":36299830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234587.1","gene_symbol":"MRPL50P1","gene_name":"mitochondrial ribosomal protein L50 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29719]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"351143","summary":null,"start":35724759,"end":35725142,"strand":-1,"description":"mitochondrial ribosomal protein L50 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29719]"}, {"versioned_ensembl_gene_id":"ENSG00000276043.4","gene_symbol":"UHRF1","gene_name":"ubiquitin like with PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:12556]","synonyms":"TDRD22,RNF106,Np95,ICBP90,FLJ21925","biotype":"protein_coding","ncbi_id":"29128","summary":"This gene encodes a member of a subfamily of RING-finger type E3 ubiquitin ligases. The protein binds to specific DNA sequences, and recruits a histone deacetylase to regulate gene expression. Its expression peaks at late G1 phase and continues during G2 and M phases of the cell cycle. It plays a major role in the G1/S transition by regulating topoisomerase IIalpha and retinoblastoma gene expression, and functions in the p53-dependent DNA damage checkpoint. It is regarded as a hub protein for the integration of epigenetic information. This gene is up-regulated in various cancers, and it is therefore considered to be a therapeutic target. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene exists on chromosome 12. [provided by RefSeq, Feb 2014]","start":4903080,"end":4962154,"strand":1,"description":"ubiquitin like with PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:12556]"}, {"versioned_ensembl_gene_id":"ENSG00000084693.15","gene_symbol":"AGBL5","gene_name":"ATP/GTP binding protein like 5 [Source:HGNC Symbol;Acc:HGNC:26147]","synonyms":"FLJ21839,CCP5","biotype":"protein_coding","ncbi_id":"60509","summary":"This gene encodes a metallocarboxypeptidase involved in protein deglutamylation and a member of the peptidase M14 family of proteins. The encoded protein has been described as a \"dual-functional\" deglutamylase that can remove glutamate residues from both carboxyl termini and side chains of protein substrates. This deglutamylase activity may be important in antiviral immunity. Mutations in this gene are associated with retinitis pigmentosa. [provided by RefSeq, Jul 2016]","start":27042364,"end":27070622,"strand":1,"description":"ATP/GTP binding protein like 5 [Source:HGNC Symbol;Acc:HGNC:26147]"}, {"versioned_ensembl_gene_id":"ENSG00000143768.12","gene_symbol":"LEFTY2","gene_name":"left-right determination factor 2 [Source:HGNC Symbol;Acc:HGNC:3122]","synonyms":"TGFB4,LEFTYA,LEFTA,EBAF","biotype":"protein_coding","ncbi_id":"7044","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which plays a role in left-right asymmetry determination of organ systems during development. The protein may also play a role in endometrial bleeding. Mutations in this gene have been associated with left-right axis malformations, particularly in the heart and lungs. Some types of infertility have been associated with dysregulated expression of this gene in the endometrium. This gene is closely linked to both a related family member and a related pseudogene. This gene encodes multiple isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]","start":225936598,"end":225941489,"strand":-1,"description":"left-right determination factor 2 [Source:HGNC Symbol;Acc:HGNC:3122]"}, {"versioned_ensembl_gene_id":"ENSG00000249787.1","gene_symbol":"AC113385.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100401441,"end":100408899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279968.2","gene_symbol":"GVQW2","gene_name":"GVQW motif containing 2 [Source:HGNC Symbol;Acc:HGNC:51715]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507462","summary":null,"start":138725211,"end":138773652,"strand":-1,"description":"GVQW motif containing 2 [Source:HGNC Symbol;Acc:HGNC:51715]"}, {"versioned_ensembl_gene_id":"ENSG00000235855.3","gene_symbol":"AP003385.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67722483,"end":67723455,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184795.9","gene_symbol":"UNC93B5","gene_name":"unc-93 homolog B5 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:34051]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729196","summary":null,"start":67711702,"end":67716005,"strand":-1,"description":"unc-93 homolog B5 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:34051]"}, {"versioned_ensembl_gene_id":"ENSG00000230215.1","gene_symbol":"LINC01840","gene_name":"long intergenic non-protein coding RNA 1840 [Source:HGNC Symbol;Acc:HGNC:40209]","synonyms":"EIF2B5-AS1","biotype":"antisense_RNA","ncbi_id":"100874079","summary":null,"start":184546714,"end":184556918,"strand":-1,"description":"long intergenic non-protein coding RNA 1840 [Source:HGNC Symbol;Acc:HGNC:40209]"}, {"versioned_ensembl_gene_id":"ENSG00000185640.5","gene_symbol":"KRT79","gene_name":"keratin 79 [Source:HGNC Symbol;Acc:HGNC:28930]","synonyms":"KRT6L,K6L","biotype":"protein_coding","ncbi_id":"338785","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes an epithelial keratin that is expressed in skeletal muscle, skin and scalp. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]","start":52821410,"end":52834295,"strand":-1,"description":"keratin 79 [Source:HGNC Symbol;Acc:HGNC:28930]"}, {"versioned_ensembl_gene_id":"ENSG00000282355.1","gene_symbol":"CARS-AS1","gene_name":"CARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100852407","summary":null,"start":3027879,"end":3040098,"strand":1,"description":"CARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40125]"}, {"versioned_ensembl_gene_id":"ENSG00000144010.9","gene_symbol":"TRIM43B","gene_name":"tripartite motif containing 43B [Source:HGNC Symbol;Acc:HGNC:37146]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653192","summary":null,"start":95476967,"end":95484731,"strand":-1,"description":"tripartite motif containing 43B [Source:HGNC Symbol;Acc:HGNC:37146]"}, {"versioned_ensembl_gene_id":"ENSG00000256050.2","gene_symbol":"AL583722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104681146,"end":104684932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247872.2","gene_symbol":"SPCS2P3","gene_name":"signal peptidase complex subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45236]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288739","summary":null,"start":816346,"end":817001,"strand":1,"description":"signal peptidase complex subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45236]"}, {"versioned_ensembl_gene_id":"ENSG00000259037.1","gene_symbol":"BX927359.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104589021,"end":104589847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269385.1","gene_symbol":"AC020895.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6898299,"end":6898686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146872.17","gene_symbol":"TLK2","gene_name":"tousled like kinase 2 [Source:HGNC Symbol;Acc:HGNC:11842]","synonyms":"PKU-ALPHA,MGC44450","biotype":"protein_coding","ncbi_id":"11011","summary":"This gene encodes a nuclear serine/threonine kinase that was first identified in Arabidopsis. The encoded protein is thought to function in the regulation of chromatin assembly in the S phase of the cell cycle by regulating the levels of a histone H3/H4 chaperone. This protein is associated with double-strand break repair of DNA damage caused by radiation. Pseudogenes of this gene are present on chromosomes 10 and 17. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":62458658,"end":62615481,"strand":1,"description":"tousled like kinase 2 [Source:HGNC Symbol;Acc:HGNC:11842]"}, {"versioned_ensembl_gene_id":"ENSG00000158517.13","gene_symbol":"NCF1","gene_name":"neutrophil cytosolic factor 1 [Source:HGNC Symbol;Acc:HGNC:7660]","synonyms":"SH3PXD1A,p47phox,NOXO2,NCF1A","biotype":"protein_coding","ncbi_id":"653361","summary":"The protein encoded by this gene is a 47 kDa cytosolic subunit of neutrophil NADPH oxidase. This oxidase is a multicomponent enzyme that is activated to produce superoxide anion. Mutations in this gene have been associated with chronic granulomatous disease. [provided by RefSeq, Jul 2008]","start":74773962,"end":74789315,"strand":1,"description":"neutrophil cytosolic factor 1 [Source:HGNC Symbol;Acc:HGNC:7660]"}, {"versioned_ensembl_gene_id":"ENSG00000060558.3","gene_symbol":"GNA15","gene_name":"G protein subunit alpha 15 [Source:HGNC Symbol;Acc:HGNC:4383]","synonyms":"GNA16","biotype":"protein_coding","ncbi_id":"2769","summary":null,"start":3136193,"end":3163769,"strand":1,"description":"G protein subunit alpha 15 [Source:HGNC Symbol;Acc:HGNC:4383]"}, {"versioned_ensembl_gene_id":"ENSG00000254464.1","gene_symbol":"OR4A3P","gene_name":"olfactory receptor family 4 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15160]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81320","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54662580,"end":54663450,"strand":1,"description":"olfactory receptor family 4 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15160]"}, {"versioned_ensembl_gene_id":"ENSG00000206356.5","gene_symbol":"AC114324.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99522311,"end":99525462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047410.13","gene_symbol":"TPR","gene_name":"translocated promoter region, nuclear basket protein [Source:HGNC Symbol;Acc:HGNC:12017]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7175","summary":"This gene encodes a large coiled-coil protein that forms intranuclear filaments attached to the inner surface of nuclear pore complexes (NPCs). The protein directly interacts with several components of the NPC. It is required for the nuclear export of mRNAs and some proteins. Oncogenic fusions of the 5' end of this gene with several different kinase genes occur in some neoplasias. [provided by RefSeq, Jul 2008]","start":186311652,"end":186375693,"strand":-1,"description":"translocated promoter region, nuclear basket protein [Source:HGNC Symbol;Acc:HGNC:12017]"}, {"versioned_ensembl_gene_id":"ENSG00000251038.1","gene_symbol":"AC090958.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11909634,"end":11910765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000025423.11","gene_symbol":"HSD17B6","gene_name":"hydroxysteroid 17-beta dehydrogenase 6 [Source:HGNC Symbol;Acc:HGNC:23316]","synonyms":"SDR9C6,RODH,HSE","biotype":"protein_coding","ncbi_id":"8630","summary":"The protein encoded by this gene has both oxidoreductase and epimerase activities and is involved in androgen catabolism. The oxidoreductase activity can convert 3 alpha-adiol to dihydrotestosterone, while the epimerase activity can convert androsterone to epi-androsterone. Both reactions use NAD+ as the preferred cofactor. This gene is a member of the retinol dehydrogenase family. [provided by RefSeq, Aug 2013]","start":56752161,"end":56787790,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 6 [Source:HGNC Symbol;Acc:HGNC:23316]"}, {"versioned_ensembl_gene_id":"ENSG00000237727.7","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"AIF-1,IBA1,Em:AF129756.17,IRT-1","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31602592,"end":31604429,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000096070.19","gene_symbol":"BRPF3","gene_name":"bromodomain and PHD finger containing 3 [Source:HGNC Symbol;Acc:HGNC:14256]","synonyms":"KIAA1286","biotype":"protein_coding","ncbi_id":"27154","summary":null,"start":36196744,"end":36232790,"strand":1,"description":"bromodomain and PHD finger containing 3 [Source:HGNC Symbol;Acc:HGNC:14256]"}, {"versioned_ensembl_gene_id":"ENSG00000255250.1","gene_symbol":"AP003059.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86727355,"end":86765265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205971.2","gene_symbol":"AC074389.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1692810,"end":1694325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259265.1","gene_symbol":"AC027088.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69037549,"end":69043565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271647.1","gene_symbol":"KRT8P47","gene_name":"keratin 8 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:44461]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644743","summary":null,"start":44103306,"end":44104703,"strand":-1,"description":"keratin 8 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:44461]"}, {"versioned_ensembl_gene_id":"ENSG00000140798.15","gene_symbol":"ABCC12","gene_name":"ATP binding cassette subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:14640]","synonyms":"MRP9","biotype":"protein_coding","ncbi_id":"94160","summary":"This gene is a member of the superfamily of ATP-binding cassette (ABC) transporters and the encoded protein contains two ATP-binding domains and 12 transmembrane regions. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies: ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White. This gene is a member of the MRP subfamily which is involved in multi-drug resistance. This gene and another subfamily member are arranged head-to-tail on chromosome 16q12.1. Increased expression of this gene is associated with breast cancer. [provided by RefSeq, Jul 2008]","start":48082973,"end":48156018,"strand":-1,"description":"ATP binding cassette subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:14640]"}, {"versioned_ensembl_gene_id":"ENSG00000259761.1","gene_symbol":"AC078905.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87042054,"end":87047161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268243.1","gene_symbol":"RPS29P30","gene_name":"ribosomal protein S29 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107987273","summary":null,"start":39644502,"end":39644612,"strand":1,"description":"ribosomal protein S29 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52363]"}, {"versioned_ensembl_gene_id":"ENSG00000276021.4","gene_symbol":"WDR81","gene_name":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]","synonyms":"FLJ33817,CAMRQ2,SORF-2,PPP1R166","biotype":"protein_coding","ncbi_id":"124997","summary":"This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":1716523,"end":1738610,"strand":1,"description":"WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]"}, {"versioned_ensembl_gene_id":"ENSG00000280511.1","gene_symbol":"AL591030.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76561328,"end":76562590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259793.1","gene_symbol":"AC013726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":233351132,"end":233353416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188755.9","gene_symbol":"TBC1D3P2","gene_name":"TBC1 domain family member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27783]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440452","summary":null,"start":62264705,"end":62275655,"strand":-1,"description":"TBC1 domain family member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27783]"}, {"versioned_ensembl_gene_id":"ENSG00000250385.1","gene_symbol":"AC106772.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":524705,"end":526594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282800.1","gene_symbol":"MIR22HG","gene_name":"MIR22 host gene [Source:HGNC Symbol;Acc:HGNC:28219]","synonyms":"DKFZp686O06159,C17orf91,MGC14376","biotype":"lincRNA","ncbi_id":"84981","summary":null,"start":1711493,"end":1717174,"strand":-1,"description":"MIR22 host gene [Source:HGNC Symbol;Acc:HGNC:28219]"}, {"versioned_ensembl_gene_id":"ENSG00000270929.1","gene_symbol":"SRD5A3P1","gene_name":"steroid 5 alpha-reductase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390203","summary":null,"start":59898185,"end":59899133,"strand":1,"description":"steroid 5 alpha-reductase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49243]"}, {"versioned_ensembl_gene_id":"ENSG00000254420.1","gene_symbol":"AP003086.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78324758,"end":78444049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241597.2","gene_symbol":"AC022121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98954394,"end":98954972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261057.1","gene_symbol":"LINC00555","gene_name":"long intergenic non-protein coding RNA 555 [Source:HGNC Symbol;Acc:HGNC:43699]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861543","summary":null,"start":102589372,"end":102589813,"strand":-1,"description":"long intergenic non-protein coding RNA 555 [Source:HGNC Symbol;Acc:HGNC:43699]"}, {"versioned_ensembl_gene_id":"ENSG00000280334.1","gene_symbol":"AC009084.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67006672,"end":67009481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258897.1","gene_symbol":"EGLN3-AS1","gene_name":"EGLN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49077]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105370445","summary":null,"start":34040097,"end":34059300,"strand":1,"description":"EGLN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49077]"}, {"versioned_ensembl_gene_id":"ENSG00000235914.1","gene_symbol":"MACROD2-AS1","gene_name":"MACROD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37193]","synonyms":"NCRNA00186,BA318C17.1","biotype":"antisense_RNA","ncbi_id":"100379174","summary":null,"start":14884253,"end":14929515,"strand":-1,"description":"MACROD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37193]"}, {"versioned_ensembl_gene_id":"ENSG00000242009.1","gene_symbol":"AC129807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81840547,"end":81922861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129515.18","gene_symbol":"SNX6","gene_name":"sorting nexin 6 [Source:HGNC Symbol;Acc:HGNC:14970]","synonyms":null,"biotype":"protein_coding","ncbi_id":"58533","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein associates with the long isoform of the leptin receptor, the transforming growth factor-beta family of receptor serine-threonine kinases, and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor. This protein may form oligomeric complexes with family member proteins through interactions of both the PX domain and the coiled coil regions of the molecules. Translocation of this protein from the cytoplasm to the nucleus occurs after binding to proviral integration site 1 protein. This gene results in two transcripts encoding two distinct isoforms. [provided by RefSeq, Jul 2008]","start":34561094,"end":34630183,"strand":-1,"description":"sorting nexin 6 [Source:HGNC Symbol;Acc:HGNC:14970]"}, {"versioned_ensembl_gene_id":"ENSG00000105398.3","gene_symbol":"SULT2A1","gene_name":"sulfotransferase family 2A member 1 [Source:HGNC Symbol;Acc:HGNC:11458]","synonyms":"STD,DHEA-ST","biotype":"protein_coding","ncbi_id":"6822","summary":"This gene encodes a member of the sulfotransferase family. Sulfotransferases aid in the metabolism of drugs and endogenous compounds by converting these substances into more hydrophilic water-soluble sulfate conjugates that can be easily excreted. This protein catalyzes the sulfation of steroids and bile acids in the liver and adrenal glands, and may have a role in the inherited adrenal androgen excess in women with polycystic ovary syndrome. [provided by RefSeq, Mar 2010]","start":47870466,"end":47886397,"strand":-1,"description":"sulfotransferase family 2A member 1 [Source:HGNC Symbol;Acc:HGNC:11458]"}, {"versioned_ensembl_gene_id":"ENSG00000256756.1","gene_symbol":"TIMM17BP1","gene_name":"translocase of inner mitochondrial membrane 17B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49865]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390298","summary":null,"start":17400399,"end":17400914,"strand":1,"description":"translocase of inner mitochondrial membrane 17B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49865]"}, {"versioned_ensembl_gene_id":"ENSG00000272576.1","gene_symbol":"AC027271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51918772,"end":51919381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225859.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"D6S81E,BAT1,UAP56","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31569699,"end":31586038,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000224691.1","gene_symbol":"AL133553.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186176814,"end":186177302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077152.9","gene_symbol":"UBE2T","gene_name":"ubiquitin conjugating enzyme E2 T [Source:HGNC Symbol;Acc:HGNC:25009]","synonyms":"HSPC150,FANCT","biotype":"protein_coding","ncbi_id":"29089","summary":"The protein encoded by this gene catalyzes the covalent attachment of ubiquitin to protein substrates. Defects in this gene have been associated with Fanconi anemia of complementation group T. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":202331657,"end":202341980,"strand":-1,"description":"ubiquitin conjugating enzyme E2 T [Source:HGNC Symbol;Acc:HGNC:25009]"}, {"versioned_ensembl_gene_id":"ENSG00000103200.6","gene_symbol":"AC069335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140435316,"end":140435787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282614.1","gene_symbol":"AC243807.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45597507,"end":45598565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229023.1","gene_symbol":"AC067945.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190992639,"end":190993567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141279.15","gene_symbol":"NPEPPS","gene_name":"aminopeptidase puromycin sensitive [Source:HGNC Symbol;Acc:HGNC:7900]","synonyms":"PSA,MP100","biotype":"protein_coding","ncbi_id":"9520","summary":"This gene encodes the puromycin-sensitive aminopeptidase, a zinc metallopeptidase which hydrolyzes amino acids from the N-terminus of its substrate. The protein has been localized to both the cytoplasm and to cellular membranes. This enzyme degrades enkaphalins in the brain, and studies in mouse suggest that it is involved in proteolytic events regulating the cell cycle. [provided by RefSeq, Jul 2008]","start":47522942,"end":47623276,"strand":1,"description":"aminopeptidase puromycin sensitive [Source:HGNC Symbol;Acc:HGNC:7900]"}, {"versioned_ensembl_gene_id":"ENSG00000234768.1","gene_symbol":"AL611929.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168194358,"end":168204501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258177.1","gene_symbol":"AC008149.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96222797,"end":96223973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168096.14","gene_symbol":"ANKS3","gene_name":"ankyrin repeat and sterile alpha motif domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29422]","synonyms":"KIAA1977,FLJ32767,FLJ32345","biotype":"protein_coding","ncbi_id":"124401","summary":null,"start":4696510,"end":4734378,"strand":-1,"description":"ankyrin repeat and sterile alpha motif domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29422]"}, {"versioned_ensembl_gene_id":"ENSG00000270469.1","gene_symbol":"AC006557.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14053951,"end":14054761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227952.2","gene_symbol":"RPL18AP17","gene_name":"ribosomal protein L18a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39850]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873859","summary":null,"start":72460132,"end":72460329,"strand":-1,"description":"ribosomal protein L18a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39850]"}, {"versioned_ensembl_gene_id":"ENSG00000272265.1","gene_symbol":"AC034236.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116078110,"end":116078570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119574.12","gene_symbol":"ZBTB45","gene_name":"zinc finger and BTB domain containing 45 [Source:HGNC Symbol;Acc:HGNC:23715]","synonyms":"ZNF499,FLJ14486","biotype":"protein_coding","ncbi_id":"84878","summary":null,"start":58513530,"end":58538911,"strand":-1,"description":"zinc finger and BTB domain containing 45 [Source:HGNC Symbol;Acc:HGNC:23715]"}, {"versioned_ensembl_gene_id":"ENSG00000185684.13","gene_symbol":"EP400NL","gene_name":"EP400 N-terminal like [Source:HGNC Symbol;Acc:HGNC:26602]","synonyms":"FLJ33915","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"347918","summary":null,"start":132084283,"end":132131639,"strand":1,"description":"EP400 N-terminal like [Source:HGNC Symbol;Acc:HGNC:26602]"}, {"versioned_ensembl_gene_id":"ENSG00000241544.1","gene_symbol":"LINC02029","gene_name":"long intergenic non-protein coding RNA 2029 [Source:HGNC Symbol;Acc:HGNC:52863]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374177","summary":null,"start":157081841,"end":157088547,"strand":1,"description":"long intergenic non-protein coding RNA 2029 [Source:HGNC Symbol;Acc:HGNC:52863]"}, {"versioned_ensembl_gene_id":"ENSG00000269106.1","gene_symbol":"AC012313.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58475355,"end":58475763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231208.4","gene_symbol":"ZBTB46-AS1","gene_name":"ZBTB46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40753]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928604","summary":null,"start":63808076,"end":63816521,"strand":1,"description":"ZBTB46 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40753]"}, {"versioned_ensembl_gene_id":"ENSG00000172824.14","gene_symbol":"CES4A","gene_name":"carboxylesterase 4A [Source:HGNC Symbol;Acc:HGNC:26741]","synonyms":"FLJ37464,CES8","biotype":"protein_coding","ncbi_id":"283848","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They also participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene, also called CES6, encodes a secreted enzyme, and may play a role in the detoxification of drugs and xenobiotics in neural and other tissues of the body and in the cerebrospinal fluid. Multiple transcript variants encoding different isoforms have been reported, but the full-length nature and/or biological validity of some variants have not been determined. [provided by RefSeq, Jun 2010]","start":66988589,"end":67009758,"strand":1,"description":"carboxylesterase 4A [Source:HGNC Symbol;Acc:HGNC:26741]"}, {"versioned_ensembl_gene_id":"ENSG00000109943.8","gene_symbol":"CRTAM","gene_name":"cytotoxic and regulatory T-cell molecule [Source:HGNC Symbol;Acc:HGNC:24313]","synonyms":"CD355","biotype":"protein_coding","ncbi_id":"56253","summary":"The CRTAM gene is upregulated in CD4 (see MIM 186940)-positive and CD8 (see CD8A; MIM 186910)-positive T cells and encodes a type I transmembrane protein with V and C1-like Ig domains (Yeh et al., 2008 [PubMed 18329370]).[supplied by OMIM, Feb 2009]","start":122838500,"end":122872639,"strand":1,"description":"cytotoxic and regulatory T-cell molecule [Source:HGNC Symbol;Acc:HGNC:24313]"}, {"versioned_ensembl_gene_id":"ENSG00000224274.1","gene_symbol":"ENSAP1","gene_name":"endosulfine alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16588]","synonyms":"ENSAP,dJ822J19.1","biotype":"processed_pseudogene","ncbi_id":"170511","summary":null,"start":15619494,"end":15619819,"strand":-1,"description":"endosulfine alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16588]"}, {"versioned_ensembl_gene_id":"ENSG00000230935.1","gene_symbol":"RPS3P1","gene_name":"ribosomal protein S3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16579]","synonyms":"dJ631M13.3","biotype":"processed_pseudogene","ncbi_id":"140754","summary":null,"start":14003508,"end":14003699,"strand":1,"description":"ribosomal protein S3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16579]"}, {"versioned_ensembl_gene_id":"ENSG00000274145.2","gene_symbol":"RILP","gene_name":"Rab interacting lysosomal protein [Source:HGNC Symbol;Acc:HGNC:30266]","synonyms":"FLJ31193","biotype":"protein_coding","ncbi_id":"83547","summary":"This gene encodes a lysosomal protein that interacts with RAB7, a small GTPase that controls transport to endocytic degradative compartments. Studies using mutant forms of the two proteins suggest that this protein represents a downstream effector for RAB7, and both proteins act together in the regulation of late endocytic traffic. A unique region of this protein has also been shown to be involved in the regulation of lysosomal morphology. [provided by RefSeq, Sep 2011]","start":1646145,"end":1650077,"strand":-1,"description":"Rab interacting lysosomal protein [Source:HGNC Symbol;Acc:HGNC:30266]"}, {"versioned_ensembl_gene_id":"ENSG00000064102.14","gene_symbol":"INTS13","gene_name":"integrator complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:20174]","synonyms":"SPATA30,NET48,Mat89Bb,FLJ10637,C12orf11,ASUN","biotype":"protein_coding","ncbi_id":"55726","summary":null,"start":26905181,"end":26938326,"strand":-1,"description":"integrator complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:20174]"}, {"versioned_ensembl_gene_id":"ENSG00000273951.1","gene_symbol":"AL031667.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41485571,"end":41486225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283646.1","gene_symbol":"LINC02009","gene_name":"long intergenic non-protein coding RNA 2009 [Source:HGNC Symbol;Acc:HGNC:52845]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377068","summary":null,"start":46416524,"end":46423591,"strand":-1,"description":"long intergenic non-protein coding RNA 2009 [Source:HGNC Symbol;Acc:HGNC:52845]"}, {"versioned_ensembl_gene_id":"ENSG00000080200.9","gene_symbol":"CRYBG3","gene_name":"crystallin beta-gamma domain containing 3 [Source:HGNC Symbol;Acc:HGNC:34427]","synonyms":"DKFZp667G2110","biotype":"protein_coding","ncbi_id":"131544","summary":null,"start":97822040,"end":97944963,"strand":1,"description":"crystallin beta-gamma domain containing 3 [Source:HGNC Symbol;Acc:HGNC:34427]"}, {"versioned_ensembl_gene_id":"ENSG00000282471.1","gene_symbol":"IGHJ3","gene_name":"immunoglobulin heavy joining 3 [Source:HGNC Symbol;Acc:HGNC:5536]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28479","summary":null,"start":105865358,"end":105865407,"strand":-1,"description":"immunoglobulin heavy joining 3 [Source:HGNC Symbol;Acc:HGNC:5536]"}, {"versioned_ensembl_gene_id":"ENSG00000272933.1","gene_symbol":"AL391121.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102642792,"end":102644140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282615.1","gene_symbol":"IGHJ5","gene_name":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28476","summary":null,"start":105864585,"end":105864635,"strand":-1,"description":"immunoglobulin heavy joining 5 [Source:HGNC Symbol;Acc:HGNC:5539]"}, {"versioned_ensembl_gene_id":"ENSG00000113262.14","gene_symbol":"GRM6","gene_name":"glutamate metabotropic receptor 6 [Source:HGNC Symbol;Acc:HGNC:4598]","synonyms":"MGLUR6,mGlu6,GPRC1F,CSNB1B","biotype":"protein_coding","ncbi_id":"2916","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Mutations in this gene result in congenital stationary night blindness type 1B. [provided by RefSeq, May 2018]","start":178978327,"end":178996206,"strand":-1,"description":"glutamate metabotropic receptor 6 [Source:HGNC Symbol;Acc:HGNC:4598]"}, {"versioned_ensembl_gene_id":"ENSG00000228292.1","gene_symbol":"AL512604.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37205112,"end":37205368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196188.10","gene_symbol":"CTSE","gene_name":"cathepsin E [Source:HGNC Symbol;Acc:HGNC:2530]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1510","summary":"This gene encodes a member of the A1 family of peptidases. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme, an aspartic endopeptidase, may be involved in antigen processing and the maturation of secretory proteins. Elevated expression of this gene has been observed in neurodegeneration. [provided by RefSeq, Nov 2015]","start":206009264,"end":206023909,"strand":-1,"description":"cathepsin E [Source:HGNC Symbol;Acc:HGNC:2530]"}, {"versioned_ensembl_gene_id":"ENSG00000272431.1","gene_symbol":"AC104117.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178938677,"end":178939223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156194.17","gene_symbol":"PPEF2","gene_name":"protein phosphatase with EF-hand domain 2 [Source:HGNC Symbol;Acc:HGNC:9244]","synonyms":"PPP7CB","biotype":"protein_coding","ncbi_id":"5470","summary":"This gene encodes a member of the serine/threonine protein phosphatase with EF-hand motif family. The protein contains a protein phosphatase catalytic domain, and at least two EF-hand calcium-binding motifs in its C terminus. Although its substrate(s) is unknown, the encoded protein, which is expressed specifically in photoreceptors and the pineal, has been suggested to play a role in the visual system. This gene shares high sequence similarity with the Drosophila retinal degeneration C (rdgC) gene. [provided by RefSeq, Jul 2008]","start":75859864,"end":75902571,"strand":-1,"description":"protein phosphatase with EF-hand domain 2 [Source:HGNC Symbol;Acc:HGNC:9244]"}, {"versioned_ensembl_gene_id":"ENSG00000167792.11","gene_symbol":"NDUFV1","gene_name":"NADH:ubiquinone oxidoreductase core subunit V1 [Source:HGNC Symbol;Acc:HGNC:7716]","synonyms":"CI-51K","biotype":"protein_coding","ncbi_id":"4723","summary":"The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]","start":67606852,"end":67612535,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit V1 [Source:HGNC Symbol;Acc:HGNC:7716]"}, {"versioned_ensembl_gene_id":"ENSG00000229805.1","gene_symbol":"LINC01813","gene_name":"long intergenic non-protein coding RNA 1813 [Source:HGNC Symbol;Acc:HGNC:52617]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927165","summary":null,"start":56077417,"end":56090382,"strand":-1,"description":"long intergenic non-protein coding RNA 1813 [Source:HGNC Symbol;Acc:HGNC:52617]"}, {"versioned_ensembl_gene_id":"ENSG00000226846.1","gene_symbol":"LINC00348","gene_name":"long intergenic non-protein coding RNA 348 [Source:HGNC Symbol;Acc:HGNC:42658]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100885781","summary":null,"start":71015141,"end":71168417,"strand":1,"description":"long intergenic non-protein coding RNA 348 [Source:HGNC Symbol;Acc:HGNC:42658]"}, {"versioned_ensembl_gene_id":"ENSG00000176584.17","gene_symbol":"DMBT1P1","gene_name":"deleted in malignant brain tumors 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49497]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375940","summary":null,"start":122729429,"end":122802665,"strand":1,"description":"deleted in malignant brain tumors 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49497]"}, {"versioned_ensembl_gene_id":"ENSG00000079435.9","gene_symbol":"LIPE","gene_name":"lipase E, hormone sensitive type [Source:HGNC Symbol;Acc:HGNC:6621]","synonyms":"HSL","biotype":"protein_coding","ncbi_id":"3991","summary":"The protein encoded by this gene has a long and a short form, generated by use of alternative translational start codons. The long form is expressed in steroidogenic tissues such as testis, where it converts cholesteryl esters to free cholesterol for steroid hormone production. The short form is expressed in adipose tissue, among others, where it hydrolyzes stored triglycerides to free fatty acids. [provided by RefSeq, Jul 2008]","start":42401507,"end":42427426,"strand":-1,"description":"lipase E, hormone sensitive type [Source:HGNC Symbol;Acc:HGNC:6621]"}, {"versioned_ensembl_gene_id":"ENSG00000248627.1","gene_symbol":"AC095059.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92833685,"end":92838842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251438.1","gene_symbol":"AC104078.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36311190,"end":36392410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204790.9","gene_symbol":"AL163540.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63974762,"end":64004155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254720.1","gene_symbol":"AC023078.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18971746,"end":18972703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248416.1","gene_symbol":"AC107464.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":722275,"end":724034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204136.10","gene_symbol":"GGTA1P","gene_name":"glycoprotein, alpha-galactosyltransferase 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:4253]","synonyms":"GLYT2,GGTA1,GGTA","biotype":"transcribed_unitary_pseudogene","ncbi_id":"2681","summary":"Alpha-1,3-galactosyltransferase (GGTA1) is an enzyme present in most mammals except man, apes, and Old World monkeys. This gene is thought to encode a truncated, non-enzymatic form of the GGTA1 protein that lacks the C-terminal catalytic domain. Aberrant expression of the GGTA1 protein in man can lead to autoimmune diseases and sometimes germ cell tumors. [provided by RefSeq, May 2020]","start":121444991,"end":121500027,"strand":-1,"description":"glycoprotein, alpha-galactosyltransferase 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:4253]"}, {"versioned_ensembl_gene_id":"ENSG00000255536.1","gene_symbol":"AC023078.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18910436,"end":18911396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277125.1","gene_symbol":"AC211476.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":73065529,"end":73077353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235757.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30623124,"end":30623393,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000250984.1","gene_symbol":"AC108082.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29795938,"end":29796268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238000.1","gene_symbol":"AC116347.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98213402,"end":98214121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124159.15","gene_symbol":"MATN4","gene_name":"matrilin 4 [Source:HGNC Symbol;Acc:HGNC:6910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8785","summary":"This gene encodes a member of von Willebrand factor A domain-containing protein family. The proteins of this family are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This family member is thought to be play a role in reorganizing and regenerating the corneal matrix in granular and lattice type I dystrophies. It may also be involved in wound healing in the dentin-pulp complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":45293445,"end":45308529,"strand":-1,"description":"matrilin 4 [Source:HGNC Symbol;Acc:HGNC:6910]"}, {"versioned_ensembl_gene_id":"ENSG00000227747.2","gene_symbol":"AC096631.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":198949016,"end":198949805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228657.1","gene_symbol":"RPL23AP58","gene_name":"ribosomal protein L23a pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:36138]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271616","summary":null,"start":102572757,"end":102573225,"strand":-1,"description":"ribosomal protein L23a pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:36138]"}, {"versioned_ensembl_gene_id":"ENSG00000228309.6","gene_symbol":"LINC01350","gene_name":"long intergenic non-protein coding RNA 1350 [Source:HGNC Symbol;Acc:HGNC:50575]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929093","summary":null,"start":185558372,"end":185628527,"strand":-1,"description":"long intergenic non-protein coding RNA 1350 [Source:HGNC Symbol;Acc:HGNC:50575]"}, {"versioned_ensembl_gene_id":"ENSG00000270430.1","gene_symbol":"AC024589.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29105568,"end":29106861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254529.1","gene_symbol":"AC023078.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18863558,"end":18864509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182400.14","gene_symbol":"TRAPPC6B","gene_name":"trafficking protein particle complex 6B [Source:HGNC Symbol;Acc:HGNC:23066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122553","summary":"TRAPPC6B is a component of TRAPP complexes, which are tethering complexes involved in vesicle transport (Kummel et al., 2005 [PubMed 16025134]).[supplied by OMIM, Mar 2008]","start":39147811,"end":39170532,"strand":-1,"description":"trafficking protein particle complex 6B [Source:HGNC Symbol;Acc:HGNC:23066]"}, {"versioned_ensembl_gene_id":"ENSG00000254403.1","gene_symbol":"OR10Y1P","gene_name":"olfactory receptor family 10 subfamily Y member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15140]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81340","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59728519,"end":59729492,"strand":1,"description":"olfactory receptor family 10 subfamily Y member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15140]"}, {"versioned_ensembl_gene_id":"ENSG00000224919.1","gene_symbol":"AL591684.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47496212,"end":47502195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255021.1","gene_symbol":"AC093496.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14272373,"end":14303845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226498.2","gene_symbol":"RPSAP21","gene_name":"ribosomal protein SA pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36928]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729079","summary":null,"start":236819634,"end":236820518,"strand":1,"description":"ribosomal protein SA pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36928]"}, {"versioned_ensembl_gene_id":"ENSG00000255384.1","gene_symbol":"AP001267.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118433121,"end":118435206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226209.1","gene_symbol":"C8orf59P1","gene_name":"chromosome 8 open reading frame 59 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481719","summary":null,"start":13308145,"end":13308447,"strand":-1,"description":"chromosome 8 open reading frame 59 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51355]"}, {"versioned_ensembl_gene_id":"ENSG00000234956.5","gene_symbol":"LINC02539","gene_name":"long intergenic non-protein coding RNA 2539 [Source:HGNC Symbol;Acc:HGNC:53572]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507406","summary":null,"start":137730170,"end":137738983,"strand":-1,"description":"long intergenic non-protein coding RNA 2539 [Source:HGNC Symbol;Acc:HGNC:53572]"}, {"versioned_ensembl_gene_id":"ENSG00000063169.10","gene_symbol":"BICRA","gene_name":"BRD4 interacting chromatin remodeling complex associated protein [Source:HGNC Symbol;Acc:HGNC:4332]","synonyms":"GLTSCR1","biotype":"protein_coding","ncbi_id":"29998","summary":null,"start":47608196,"end":47703277,"strand":1,"description":"BRD4 interacting chromatin remodeling complex associated protein [Source:HGNC Symbol;Acc:HGNC:4332]"}, {"versioned_ensembl_gene_id":"ENSG00000227600.11","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32160569,"end":32179650,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000237764.2","gene_symbol":"AC010099.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125172218,"end":125379321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259999.1","gene_symbol":"AC009054.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75321890,"end":75325048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261717.5","gene_symbol":"AC009163.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":75412684,"end":75464706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248408.1","gene_symbol":"LINC02469","gene_name":"long intergenic non-protein coding RNA 2469 [Source:HGNC Symbol;Acc:HGNC:53408]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377301","summary":null,"start":79663761,"end":79696837,"strand":1,"description":"long intergenic non-protein coding RNA 2469 [Source:HGNC Symbol;Acc:HGNC:53408]"}, {"versioned_ensembl_gene_id":"ENSG00000265303.1","gene_symbol":"AC099850.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":59197566,"end":59215226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131269.15","gene_symbol":"ABCB7","gene_name":"ATP binding cassette subfamily B member 7 [Source:HGNC Symbol;Acc:HGNC:48]","synonyms":"EST140535,Atm1p,ASAT,ABC7","biotype":"protein_coding","ncbi_id":"22","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a half-transporter involved in the transport of heme from the mitochondria to the cytosol. With iron/sulfur cluster precursors as its substrates, this protein may play a role in metal homeostasis. Mutations in this gene have been associated with mitochondrial iron accumulation and isodicentric (X)(q13) and sideroblastic anemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]","start":75053172,"end":75156732,"strand":-1,"description":"ATP binding cassette subfamily B member 7 [Source:HGNC Symbol;Acc:HGNC:48]"}, {"versioned_ensembl_gene_id":"ENSG00000166822.12","gene_symbol":"TMEM170A","gene_name":"transmembrane protein 170A [Source:HGNC Symbol;Acc:HGNC:29577]","synonyms":"TMEM170,FLJ37611","biotype":"protein_coding","ncbi_id":"124491","summary":null,"start":75443054,"end":75465497,"strand":-1,"description":"transmembrane protein 170A [Source:HGNC Symbol;Acc:HGNC:29577]"}, {"versioned_ensembl_gene_id":"ENSG00000027697.13","gene_symbol":"IFNGR1","gene_name":"interferon gamma receptor 1 [Source:HGNC Symbol;Acc:HGNC:5439]","synonyms":"IFNGR,CD119","biotype":"protein_coding","ncbi_id":"3459","summary":"This gene (IFNGR1) encodes the ligand-binding chain (alpha) of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection. In addition, defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease, also known as familial disseminated atypical mycobacterial infection. [provided by RefSeq, Jul 2008]","start":137197484,"end":137219449,"strand":-1,"description":"interferon gamma receptor 1 [Source:HGNC Symbol;Acc:HGNC:5439]"}, {"versioned_ensembl_gene_id":"ENSG00000196553.15","gene_symbol":"CCDC196","gene_name":"coiled-coil domain containing 196 [Source:HGNC Symbol;Acc:HGNC:20100]","synonyms":"LINC00238,C14orf53,NCRNA00238","biotype":"protein_coding","ncbi_id":"440184","summary":null,"start":66411704,"end":66498677,"strand":1,"description":"coiled-coil domain containing 196 [Source:HGNC Symbol;Acc:HGNC:20100]"}, {"versioned_ensembl_gene_id":"ENSG00000258796.1","gene_symbol":"AL133241.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66760532,"end":66761018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145912.8","gene_symbol":"NHP2","gene_name":"NHP2 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14377]","synonyms":"NOLA2,FLJ20479","biotype":"protein_coding","ncbi_id":"55651","summary":"This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA1 and NOLA3 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. The four H/ACA snoRNP proteins are also components of the telomerase complex. This gene encodes a protein related to Saccharomyces cerevisiae Nhp2p. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008]","start":178149460,"end":178153967,"strand":-1,"description":"NHP2 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14377]"}, {"versioned_ensembl_gene_id":"ENSG00000178828.6","gene_symbol":"RNF186","gene_name":"ring finger protein 186 [Source:HGNC Symbol;Acc:HGNC:25978]","synonyms":"FLJ20225","biotype":"protein_coding","ncbi_id":"54546","summary":null,"start":19814029,"end":19815278,"strand":-1,"description":"ring finger protein 186 [Source:HGNC Symbol;Acc:HGNC:25978]"}, {"versioned_ensembl_gene_id":"ENSG00000231419.6","gene_symbol":"LINC00689","gene_name":"long intergenic non-protein coding RNA 689 [Source:HGNC Symbol;Acc:HGNC:27217]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"154822","summary":null,"start":159006522,"end":159030195,"strand":1,"description":"long intergenic non-protein coding RNA 689 [Source:HGNC Symbol;Acc:HGNC:27217]"}, {"versioned_ensembl_gene_id":"ENSG00000277500.1","gene_symbol":"AC026951.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31787494,"end":31787734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235434.1","gene_symbol":"AL391883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19814367,"end":19819502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258980.1","gene_symbol":"EIF1AXP2","gene_name":"eukaryotic translation initiation factor 1A, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44295]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479036","summary":null,"start":65528830,"end":65529574,"strand":-1,"description":"eukaryotic translation initiation factor 1A, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44295]"}, {"versioned_ensembl_gene_id":"ENSG00000242137.1","gene_symbol":"AC063943.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120594015,"end":120594548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259827.1","gene_symbol":"AC026461.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":56682470,"end":56687807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006715.15","gene_symbol":"VPS41","gene_name":"VPS41, HOPS complex subunit [Source:HGNC Symbol;Acc:HGNC:12713]","synonyms":"HVSP41","biotype":"protein_coding","ncbi_id":"27072","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human ortholog of yeast Vps41 protein which is also conserved in Drosophila, tomato, and Arabidopsis. Expression studies in yeast and human indicate that this protein may be involved in the formation and fusion of transport vesicles from the Golgi. Several transcript variants encoding different isoforms have been described for this gene, however, the full-length nature of not all is known. [provided by RefSeq, Jul 2008]","start":38722963,"end":38932394,"strand":-1,"description":"VPS41, HOPS complex subunit [Source:HGNC Symbol;Acc:HGNC:12713]"}, {"versioned_ensembl_gene_id":"ENSG00000258956.2","gene_symbol":"COX4I1P1","gene_name":"cytochrome c oxidase subunit 4I1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2266]","synonyms":"COX4P1,COX4L1","biotype":"processed_pseudogene","ncbi_id":"122867","summary":null,"start":61831861,"end":61832369,"strand":-1,"description":"cytochrome c oxidase subunit 4I1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2266]"}, {"versioned_ensembl_gene_id":"ENSG00000223500.1","gene_symbol":"AC083862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135128444,"end":135129685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119777.18","gene_symbol":"TMEM214","gene_name":"transmembrane protein 214 [Source:HGNC Symbol;Acc:HGNC:25983]","synonyms":"FLJ20254","biotype":"protein_coding","ncbi_id":"54867","summary":null,"start":27032910,"end":27041695,"strand":1,"description":"transmembrane protein 214 [Source:HGNC Symbol;Acc:HGNC:25983]"}, {"versioned_ensembl_gene_id":"ENSG00000159063.12","gene_symbol":"ALG8","gene_name":"ALG8, alpha-1,3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23161]","synonyms":"MGC2840","biotype":"protein_coding","ncbi_id":"79053","summary":"This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":78100936,"end":78139660,"strand":-1,"description":"ALG8, alpha-1,3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23161]"}, {"versioned_ensembl_gene_id":"ENSG00000154059.9","gene_symbol":"IMPACT","gene_name":"impact RWD domain protein [Source:HGNC Symbol;Acc:HGNC:20387]","synonyms":"RWDD5","biotype":"protein_coding","ncbi_id":"55364","summary":null,"start":24426616,"end":24453535,"strand":1,"description":"impact RWD domain protein [Source:HGNC Symbol;Acc:HGNC:20387]"}, {"versioned_ensembl_gene_id":"ENSG00000233439.8","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"SEEK1,C6orf16","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31108521,"end":31133775,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000196605.7","gene_symbol":"ZNF846","gene_name":"zinc finger protein 846 [Source:HGNC Symbol;Acc:HGNC:27260]","synonyms":null,"biotype":"protein_coding","ncbi_id":"162993","summary":null,"start":9751993,"end":9793180,"strand":-1,"description":"zinc finger protein 846 [Source:HGNC Symbol;Acc:HGNC:27260]"}, {"versioned_ensembl_gene_id":"ENSG00000225391.5","gene_symbol":"NHEG1","gene_name":"neuroblastoma highly expressed 1 [Source:NCBI gene;Acc:100294720]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100294720","summary":null,"start":136982165,"end":136993234,"strand":-1,"description":"neuroblastoma highly expressed 1 [Source:NCBI gene;Acc:100294720]"}, {"versioned_ensembl_gene_id":"ENSG00000139200.13","gene_symbol":"PIANP","gene_name":"PILR alpha associated neural protein [Source:HGNC Symbol;Acc:HGNC:25338]","synonyms":"PANP,DKFZp547D2210,C12orf53","biotype":"protein_coding","ncbi_id":"196500","summary":"This gene encodes a ligand for the paired immunoglobin-like type 2 receptor alpha, and so may be involved in immune regulation. Alternate splicing results in multiple transcript variants encoding different proteins. [provided by RefSeq, Sep 2011]","start":6693792,"end":6700800,"strand":-1,"description":"PILR alpha associated neural protein [Source:HGNC Symbol;Acc:HGNC:25338]"}, {"versioned_ensembl_gene_id":"ENSG00000267302.5","gene_symbol":"AC005702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59964832,"end":59996972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241913.1","gene_symbol":"RPS29P21","gene_name":"ribosomal protein S29 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36479]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129542","summary":null,"start":59912197,"end":59912366,"strand":1,"description":"ribosomal protein S29 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36479]"}, {"versioned_ensembl_gene_id":"ENSG00000230018.1","gene_symbol":"AL133482.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113482616,"end":113483113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280912.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000100403.11","gene_symbol":"ZC3H7B","gene_name":"zinc finger CCCH-type containing 7B [Source:HGNC Symbol;Acc:HGNC:30869]","synonyms":"RoXaN,KIAA1031,FLJ13787,DKFZp434K0920","biotype":"protein_coding","ncbi_id":"23264","summary":"This gene encodes a protein that contains a tetratricopeptide repeat domain. The encoded protein also interacts with the rotavirus non-structural protein NSP3. [provided by RefSeq, Jul 2008]","start":41301522,"end":41360147,"strand":1,"description":"zinc finger CCCH-type containing 7B [Source:HGNC Symbol;Acc:HGNC:30869]"}, {"versioned_ensembl_gene_id":"ENSG00000139990.17","gene_symbol":"DCAF5","gene_name":"DDB1 and CUL4 associated factor 5 [Source:HGNC Symbol;Acc:HGNC:20224]","synonyms":"WDR22,KIAA1824,D14S1461E,BCRP2,BCRG2","biotype":"protein_coding","ncbi_id":"8816","summary":null,"start":69050881,"end":69153150,"strand":-1,"description":"DDB1 and CUL4 associated factor 5 [Source:HGNC Symbol;Acc:HGNC:20224]"}, {"versioned_ensembl_gene_id":"ENSG00000276045.2","gene_symbol":"ORAI1","gene_name":"ORAI calcium release-activated calcium modulator 1 [Source:HGNC Symbol;Acc:HGNC:25896]","synonyms":"TMEM142A,FLJ14466,CRACM1","biotype":"protein_coding","ncbi_id":"84876","summary":"The protein encoded by this gene is a membrane calcium channel subunit that is activated by the calcium sensor STIM1 when calcium stores are depleted. This type of channel is the primary way for calcium influx into T-cells. Defects in this gene are a cause of immune dysfunction with T-cell inactivation due to calcium entry defect type 1 (IDTICED1). [provided by RefSeq, Sep 2011]","start":121626550,"end":121642677,"strand":1,"description":"ORAI calcium release-activated calcium modulator 1 [Source:HGNC Symbol;Acc:HGNC:25896]"}, {"versioned_ensembl_gene_id":"ENSG00000180662.8","gene_symbol":"RPL21P8","gene_name":"ribosomal protein L21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:19779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319145","summary":null,"start":65467807,"end":65468341,"strand":-1,"description":"ribosomal protein L21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:19779]"}, {"versioned_ensembl_gene_id":"ENSG00000265163.1","gene_symbol":"CDRT8","gene_name":"CMT1A duplicated region transcript 8 [Source:HGNC Symbol;Acc:HGNC:14387]","synonyms":null,"biotype":"lincRNA","ncbi_id":"94151","summary":null,"start":15105237,"end":15106187,"strand":-1,"description":"CMT1A duplicated region transcript 8 [Source:HGNC Symbol;Acc:HGNC:14387]"}, {"versioned_ensembl_gene_id":"ENSG00000232998.1","gene_symbol":"VPS13A-AS1","gene_name":"VPS13A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44167]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100286938","summary":null,"start":77176756,"end":77177994,"strand":-1,"description":"VPS13A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44167]"}, {"versioned_ensembl_gene_id":"ENSG00000073605.18","gene_symbol":"GSDMB","gene_name":"gasdermin B [Source:HGNC Symbol;Acc:HGNC:23690]","synonyms":"PRO2521,GSDML","biotype":"protein_coding","ncbi_id":"55876","summary":"This gene encodes a member of the gasdermin-domain containing protein family. Other gasdermin-family genes are implicated in the regulation of apoptosis in epithelial cells, and are linked to cancer. Alternative splicing and the use of alternative promoters results in multiple transcript variants. Additional variants have been described, but they are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to be protein-coding. [provided by RefSeq, Nov 2016]","start":39904595,"end":39919854,"strand":-1,"description":"gasdermin B [Source:HGNC Symbol;Acc:HGNC:23690]"}, {"versioned_ensembl_gene_id":"ENSG00000147127.8","gene_symbol":"RAB41","gene_name":"RAB41, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18293]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347517","summary":"This gene encodes a small GTP-binding protein that belongs to the largest family within the Ras superfamily. These proteins function as regulators of membrane trafficking. They cycle between inactive GDP-bound and activated GTP-bound states, which is controlled by GTP hydrolysis-activating proteins (GAPs). This family member can be activated by the GAP protein RN-Tre, and it is localized to the Golgi complex. [provided by RefSeq, May 2010]","start":70282093,"end":70285002,"strand":1,"description":"RAB41, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18293]"}, {"versioned_ensembl_gene_id":"ENSG00000186466.5","gene_symbol":"AQP7P1","gene_name":"aquaporin 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32048]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"375719","summary":null,"start":63317067,"end":63333091,"strand":-1,"description":"aquaporin 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32048]"}, {"versioned_ensembl_gene_id":"ENSG00000272143.1","gene_symbol":"FGF14-AS2","gene_name":"FGF14 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44368]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283481","summary":null,"start":102394630,"end":102395703,"strand":1,"description":"FGF14 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44368]"}, {"versioned_ensembl_gene_id":"ENSG00000155906.16","gene_symbol":"RMND1","gene_name":"required for meiotic nuclear division 1 homolog [Source:HGNC Symbol;Acc:HGNC:21176]","synonyms":"RMD1,FLJ20627,C6orf96,bA351K16.3","biotype":"protein_coding","ncbi_id":"55005","summary":"The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]","start":151404763,"end":151452181,"strand":-1,"description":"required for meiotic nuclear division 1 homolog [Source:HGNC Symbol;Acc:HGNC:21176]"}, {"versioned_ensembl_gene_id":"ENSG00000175229.6","gene_symbol":"GAL3ST3","gene_name":"galactose-3-O-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:24144]","synonyms":"GAL3ST2","biotype":"protein_coding","ncbi_id":"89792","summary":"This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the 3' position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans, but not on type 1 or core-1-branched structures. This gene, which has also been referred to as GAL3ST2, is different from the GAL3ST2 gene located on chromosome 2 that encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 3. [provided by RefSeq, Jul 2008]","start":66041952,"end":66049180,"strand":-1,"description":"galactose-3-O-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:24144]"}, {"versioned_ensembl_gene_id":"ENSG00000188991.3","gene_symbol":"SLC15A5","gene_name":"solute carrier family 15 member 5 [Source:HGNC Symbol;Acc:HGNC:33455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729025","summary":null,"start":16188485,"end":16277685,"strand":-1,"description":"solute carrier family 15 member 5 [Source:HGNC Symbol;Acc:HGNC:33455]"}, {"versioned_ensembl_gene_id":"ENSG00000205231.1","gene_symbol":"TTLL10-AS1","gene_name":"TTLL10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41159]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506376","summary":null,"start":1173056,"end":1179555,"strand":-1,"description":"TTLL10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41159]"}, {"versioned_ensembl_gene_id":"ENSG00000279145.1","gene_symbol":"AC011912.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":55171972,"end":55178175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267175.5","gene_symbol":"AC105094.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61592375,"end":61748832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267409.1","gene_symbol":"AC068473.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79610747,"end":79612303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167797.7","gene_symbol":"CDK2AP2","gene_name":"cyclin dependent kinase 2 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:30833]","synonyms":"p14,DOC-1R","biotype":"protein_coding","ncbi_id":"10263","summary":"This gene encodes a protein that interacts with cyclin-dependent kinase 2 associated protein 1. Pseudogenes associated with this gene are located on chromosomes 7 and 9. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2012]","start":67506497,"end":67508649,"strand":-1,"description":"cyclin dependent kinase 2 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:30833]"}, {"versioned_ensembl_gene_id":"ENSG00000143933.16","gene_symbol":"CALM2","gene_name":"calmodulin 2 [Source:HGNC Symbol;Acc:HGNC:1445]","synonyms":"PHKD,CAMII","biotype":"protein_coding","ncbi_id":"805","summary":"This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role in signaling pathways, cell cycle progression and proliferation. Several infants with severe forms of long-QT syndrome (LQTS) who displayed life-threatening ventricular arrhythmias together with delayed neurodevelopment and epilepsy were found to have mutations in either this gene or another member of the calmodulin gene family (PMID:23388215). Mutations in this gene have also been identified in patients with less severe forms of LQTS (PMID:24917665), while mutations in another calmodulin gene family member have been associated with catecholaminergic polymorphic ventricular tachycardia (CPVT)(PMID:23040497), a rare disorder thought to be the cause of a significant fraction of sudden cardiac deaths in young individuals. Pseudogenes of this gene are found on chromosomes 10, 13, and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]","start":47160082,"end":47176601,"strand":-1,"description":"calmodulin 2 [Source:HGNC Symbol;Acc:HGNC:1445]"}, {"versioned_ensembl_gene_id":"ENSG00000228163.8","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33218673,"end":33234885,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000247193.2","gene_symbol":"AC104078.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36244116,"end":36274220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271597.1","gene_symbol":"AC112230.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69251818,"end":69252364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151364.16","gene_symbol":"KCTD14","gene_name":"potassium channel tetramerization domain containing 14 [Source:HGNC Symbol;Acc:HGNC:23295]","synonyms":"MGC2376","biotype":"protein_coding","ncbi_id":"65987","summary":null,"start":78015715,"end":78046191,"strand":-1,"description":"potassium channel tetramerization domain containing 14 [Source:HGNC Symbol;Acc:HGNC:23295]"}, {"versioned_ensembl_gene_id":"ENSG00000129749.3","gene_symbol":"CHRNA10","gene_name":"cholinergic receptor nicotinic alpha 10 subunit [Source:HGNC Symbol;Acc:HGNC:13800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57053","summary":null,"start":3665587,"end":3671384,"strand":-1,"description":"cholinergic receptor nicotinic alpha 10 subunit [Source:HGNC Symbol;Acc:HGNC:13800]"}, {"versioned_ensembl_gene_id":"ENSG00000238043.1","gene_symbol":"AC024559.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":193980614,"end":194006098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269318.1","gene_symbol":"AC007292.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4356637,"end":4358448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267119.1","gene_symbol":"RPL10P15","gene_name":"ribosomal protein L10 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52347]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129975","summary":null,"start":9820141,"end":9820455,"strand":1,"description":"ribosomal protein L10 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52347]"}, {"versioned_ensembl_gene_id":"ENSG00000242986.2","gene_symbol":"RPL21P99","gene_name":"ribosomal protein L21 pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:36628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271429","summary":null,"start":29658376,"end":29658798,"strand":-1,"description":"ribosomal protein L21 pseudogene 99 [Source:HGNC Symbol;Acc:HGNC:36628]"}, {"versioned_ensembl_gene_id":"ENSG00000129596.4","gene_symbol":"CDO1","gene_name":"cysteine dioxygenase type 1 [Source:HGNC Symbol;Acc:HGNC:1795]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1036","summary":null,"start":115804733,"end":115816954,"strand":-1,"description":"cysteine dioxygenase type 1 [Source:HGNC Symbol;Acc:HGNC:1795]"}, {"versioned_ensembl_gene_id":"ENSG00000123600.19","gene_symbol":"METTL8","gene_name":"methyltransferase like 8 [Source:HGNC Symbol;Acc:HGNC:25856]","synonyms":"TIP,FLJ13984","biotype":"protein_coding","ncbi_id":"79828","summary":null,"start":171317405,"end":171434802,"strand":-1,"description":"methyltransferase like 8 [Source:HGNC Symbol;Acc:HGNC:25856]"}, {"versioned_ensembl_gene_id":"ENSG00000280087.1","gene_symbol":"AC011481.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44909375,"end":44914968,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004777.18","gene_symbol":"ARHGAP33","gene_name":"Rho GTPase activating protein 33 [Source:HGNC Symbol;Acc:HGNC:23085]","synonyms":"TCGAP,SNX26,FLJ39019","biotype":"protein_coding","ncbi_id":"115703","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Alternative splice variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]","start":35774532,"end":35788822,"strand":1,"description":"Rho GTPase activating protein 33 [Source:HGNC Symbol;Acc:HGNC:23085]"}, {"versioned_ensembl_gene_id":"ENSG00000283697.2","gene_symbol":"HSFX3","gene_name":"heat shock transcription factor family, X-linked member 3 [Source:HGNC Symbol;Acc:HGNC:52395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928917","summary":null,"start":149548210,"end":149549932,"strand":-1,"description":"heat shock transcription factor family, X-linked member 3 [Source:HGNC Symbol;Acc:HGNC:52395]"}, {"versioned_ensembl_gene_id":"ENSG00000176289.4","gene_symbol":"IDSP1","gene_name":"iduronate 2-sulfatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5390]","synonyms":"IDS2","biotype":"unprocessed_pseudogene","ncbi_id":"3424","summary":null,"start":149525001,"end":149526043,"strand":1,"description":"iduronate 2-sulfatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5390]"}, {"versioned_ensembl_gene_id":"ENSG00000238039.1","gene_symbol":"AC244197.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149511509,"end":149526264,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204612.1","gene_symbol":"FOXB2","gene_name":"forkhead box B2 [Source:HGNC Symbol;Acc:HGNC:23315]","synonyms":"bA159H20.4","biotype":"protein_coding","ncbi_id":"442425","summary":null,"start":77019655,"end":77020953,"strand":1,"description":"forkhead box B2 [Source:HGNC Symbol;Acc:HGNC:23315]"}, {"versioned_ensembl_gene_id":"ENSG00000281093.1","gene_symbol":"NCF4-AS1","gene_name":"NCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40393]","synonyms":"CTA-833B7.2","biotype":"antisense_RNA","ncbi_id":"107985578","summary":null,"start":36847372,"end":36873605,"strand":-1,"description":"NCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40393]"}, {"versioned_ensembl_gene_id":"ENSG00000170088.13","gene_symbol":"TMEM192","gene_name":"transmembrane protein 192 [Source:HGNC Symbol;Acc:HGNC:26775]","synonyms":"FLJ38482","biotype":"protein_coding","ncbi_id":"201931","summary":null,"start":165070608,"end":165208549,"strand":-1,"description":"transmembrane protein 192 [Source:HGNC Symbol;Acc:HGNC:26775]"}, {"versioned_ensembl_gene_id":"ENSG00000282580.1","gene_symbol":"AC004980.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76646507,"end":76684889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146955.10","gene_symbol":"RAB19","gene_name":"RAB19, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:19982]","synonyms":"RAB19B","biotype":"protein_coding","ncbi_id":"401409","summary":null,"start":140404043,"end":140426250,"strand":1,"description":"RAB19, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:19982]"}, {"versioned_ensembl_gene_id":"ENSG00000260496.3","gene_symbol":"AC009041.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":991151,"end":1000926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213956.4","gene_symbol":"AC112187.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50633124,"end":50633602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234634.1","gene_symbol":"LINC02093","gene_name":"long intergenic non-protein coding RNA 2093 [Source:HGNC Symbol;Acc:HGNC:52944]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371541","summary":null,"start":13299184,"end":13306760,"strand":-1,"description":"long intergenic non-protein coding RNA 2093 [Source:HGNC Symbol;Acc:HGNC:52944]"}, {"versioned_ensembl_gene_id":"ENSG00000237451.3","gene_symbol":"CDK2AP2P2","gene_name":"cyclin dependent kinase 2 associated protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107133486","summary":null,"start":62844818,"end":62845184,"strand":1,"description":"cyclin dependent kinase 2 associated protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38493]"}, {"versioned_ensembl_gene_id":"ENSG00000235803.1","gene_symbol":"MTCO2P23","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52152]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075192","summary":null,"start":69590583,"end":69591262,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52152]"}, {"versioned_ensembl_gene_id":"ENSG00000230665.3","gene_symbol":"THAP12P1","gene_name":"THAP domain containing 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39563]","synonyms":"PRKRIRP1","biotype":"processed_pseudogene","ncbi_id":"728748","summary":null,"start":74396871,"end":74399550,"strand":-1,"description":"THAP domain containing 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39563]"}, {"versioned_ensembl_gene_id":"ENSG00000271498.1","gene_symbol":"AL360085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112825939,"end":112826470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179994.10","gene_symbol":"SPDYE7P","gene_name":"speedy/RINGO cell cycle regulator family member E7, pseudogene [Source:HGNC Symbol;Acc:HGNC:35466]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441251","summary":null,"start":72862757,"end":72870510,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E7, pseudogene [Source:HGNC Symbol;Acc:HGNC:35466]"}, {"versioned_ensembl_gene_id":"ENSG00000162733.16","gene_symbol":"DDR2","gene_name":"discoidin domain receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:2731]","synonyms":"TYRO10,TKT,NTRKR3","biotype":"protein_coding","ncbi_id":"4921","summary":"This gene encodes a member of the discoidin domain receptor subclass of the receptor tyrosine kinase (RTKs) protein family. RTKs play a key role in the communication of cells with their microenvironment. The encoded protein is a collagen-induced receptor that activates signal transduction pathways involved in cell adhesion, proliferation, and extracellular matrix remodeling. This protein is expressed in numerous cell types and may alos be involved in wound repair and regulate tumor growth and invasiveness. Mutations in this gene are the cause of short limb-hand type spondylometaepiphyseal dysplasia. [provided by RefSeq, Aug 2017]","start":162631373,"end":162787400,"strand":1,"description":"discoidin domain receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:2731]"}, {"versioned_ensembl_gene_id":"ENSG00000102387.15","gene_symbol":"TAF7L","gene_name":"TATA-box binding protein associated factor 7 like [Source:HGNC Symbol;Acc:HGNC:11548]","synonyms":"TAF2Q,CT40","biotype":"protein_coding","ncbi_id":"54457","summary":"This gene is similar to a mouse gene that encodes a TATA box binding protein-associated factor, and shows testis-specific expression. The encoded protein could be a spermatogenesis-specific component of the DNA-binding general transcription factor complex TFIID. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":101268253,"end":101293057,"strand":-1,"description":"TATA-box binding protein associated factor 7 like [Source:HGNC Symbol;Acc:HGNC:11548]"}, {"versioned_ensembl_gene_id":"ENSG00000176979.12","gene_symbol":"TRIM60","gene_name":"tripartite motif containing 60 [Source:HGNC Symbol;Acc:HGNC:21162]","synonyms":"RNF33,RNF129,FLJ35882","biotype":"protein_coding","ncbi_id":"166655","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Pseudogenes of this gene are located on more than six chromosomes including chromosome 4. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]","start":165031953,"end":165041744,"strand":1,"description":"tripartite motif containing 60 [Source:HGNC Symbol;Acc:HGNC:21162]"}, {"versioned_ensembl_gene_id":"ENSG00000260570.1","gene_symbol":"AC133550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28830612,"end":28837200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267612.1","gene_symbol":"AC008759.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9730853,"end":9731943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050165.17","gene_symbol":"DKK3","gene_name":"dickkopf WNT signaling pathway inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:2893]","synonyms":"RIG,REIC","biotype":"protein_coding","ncbi_id":"27122","summary":"This gene encodes a protein that is a member of the dickkopf family. The secreted protein contains two cysteine rich regions and is involved in embryonic development through its interactions with the Wnt signaling pathway. The expression of this gene is decreased in a variety of cancer cell lines and it may function as a tumor suppressor gene. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":11963106,"end":12009769,"strand":-1,"description":"dickkopf WNT signaling pathway inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:2893]"}, {"versioned_ensembl_gene_id":"ENSG00000224689.9","gene_symbol":"ZNF812P","gene_name":"zinc finger protein 812, pseudogene [Source:HGNC Symbol;Acc:HGNC:33242]","synonyms":"ZNF812","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729648","summary":null,"start":9689924,"end":9700776,"strand":-1,"description":"zinc finger protein 812, pseudogene [Source:HGNC Symbol;Acc:HGNC:33242]"}, {"versioned_ensembl_gene_id":"ENSG00000142513.5","gene_symbol":"ACP4","gene_name":"acid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:14376]","synonyms":"ACPT","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50790415,"end":50795224,"strand":1,"description":"acid phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:14376]"}, {"versioned_ensembl_gene_id":"ENSG00000117676.13","gene_symbol":"RPS6KA1","gene_name":"ribosomal protein S6 kinase A1 [Source:HGNC Symbol;Acc:HGNC:10430]","synonyms":"RSK,p90Rsk,HU-1,RSK1","biotype":"protein_coding","ncbi_id":"6195","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 nonidentical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":26529761,"end":26575030,"strand":1,"description":"ribosomal protein S6 kinase A1 [Source:HGNC Symbol;Acc:HGNC:10430]"}, {"versioned_ensembl_gene_id":"ENSG00000023608.4","gene_symbol":"SNAPC1","gene_name":"small nuclear RNA activating complex polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:11134]","synonyms":"SNAP43,PTFgamma","biotype":"protein_coding","ncbi_id":"6617","summary":null,"start":61762357,"end":61796428,"strand":1,"description":"small nuclear RNA activating complex polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:11134]"}, {"versioned_ensembl_gene_id":"ENSG00000258777.1","gene_symbol":"HIF1A-AS1","gene_name":"HIF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43014]","synonyms":"5'aHIF-1A","biotype":"lincRNA","ncbi_id":"100750246","summary":null,"start":61681041,"end":61695823,"strand":-1,"description":"HIF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43014]"}, {"versioned_ensembl_gene_id":"ENSG00000226117.1","gene_symbol":"AC090844.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39839369,"end":39839524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260428.2","gene_symbol":"SCX","gene_name":"scleraxis bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:32322]","synonyms":"SCXB,SCXA,bHLHa48,bHLHa41","biotype":"protein_coding","ncbi_id":"642658","summary":null,"start":144266560,"end":144268481,"strand":1,"description":"scleraxis bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:32322]"}, {"versioned_ensembl_gene_id":"ENSG00000227420.8","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"HSPC183,PTD017,C6orf14,MRPS18-2","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30607552,"end":30616238,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000248874.5","gene_symbol":"C5orf17","gene_name":"chromosome 5 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:26630]","synonyms":"FLJ34836","biotype":"lincRNA","ncbi_id":"439936","summary":null,"start":23951348,"end":24178263,"strand":1,"description":"chromosome 5 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:26630]"}, {"versioned_ensembl_gene_id":"ENSG00000257599.2","gene_symbol":"OVCH1-AS1","gene_name":"OVCH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44484]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101055625","summary":null,"start":29389289,"end":29487488,"strand":1,"description":"OVCH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44484]"}, {"versioned_ensembl_gene_id":"ENSG00000249607.1","gene_symbol":"AC108103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23688927,"end":23689386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269565.1","gene_symbol":"GPR32P1","gene_name":"G protein-coupled receptor 32, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4488]","synonyms":"GPR32P","biotype":"unprocessed_pseudogene","ncbi_id":"2855","summary":null,"start":50758382,"end":50759192,"strand":1,"description":"G protein-coupled receptor 32, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4488]"}, {"versioned_ensembl_gene_id":"ENSG00000230185.4","gene_symbol":"C9orf147","gene_name":"chromosome 9 open reading frame 147 [Source:HGNC Symbol;Acc:HGNC:31438]","synonyms":"bA32M23.3","biotype":"antisense_RNA","ncbi_id":"100133204","summary":null,"start":112433816,"end":112487204,"strand":-1,"description":"chromosome 9 open reading frame 147 [Source:HGNC Symbol;Acc:HGNC:31438]"}, {"versioned_ensembl_gene_id":"ENSG00000250068.1","gene_symbol":"AL445187.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":112581779,"end":112582590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173698.17","gene_symbol":"ADGRG2","gene_name":"adhesion G protein-coupled receptor G2 [Source:HGNC Symbol;Acc:HGNC:4516]","synonyms":"TM7LN2,HE6,GPR64,EDDM6","biotype":"protein_coding","ncbi_id":"10149","summary":"This gene encodes a member of the G protein-coupled receptor family described as an epididymis-specific transmembrane protein. The encoded protein may be proteolytically processed as it contains a motif shown to be a protein scission motif in some members of this family (PMID: 11973329). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":18989309,"end":19122637,"strand":-1,"description":"adhesion G protein-coupled receptor G2 [Source:HGNC Symbol;Acc:HGNC:4516]"}, {"versioned_ensembl_gene_id":"ENSG00000108395.13","gene_symbol":"TRIM37","gene_name":"tripartite motif containing 37 [Source:HGNC Symbol;Acc:HGNC:7523]","synonyms":"TEF3,POB1,MUL,KIAA0898","biotype":"protein_coding","ncbi_id":"4591","summary":"This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020]","start":58982638,"end":59106921,"strand":-1,"description":"tripartite motif containing 37 [Source:HGNC Symbol;Acc:HGNC:7523]"}, {"versioned_ensembl_gene_id":"ENSG00000241462.1","gene_symbol":"AC100832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58897776,"end":58899692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250334.5","gene_symbol":"LINC00989","gene_name":"long intergenic non-protein coding RNA 989 [Source:HGNC Symbol;Acc:HGNC:48918]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506035","summary":null,"start":79492416,"end":79576460,"strand":1,"description":"long intergenic non-protein coding RNA 989 [Source:HGNC Symbol;Acc:HGNC:48918]"}, {"versioned_ensembl_gene_id":"ENSG00000137766.16","gene_symbol":"UNC13C","gene_name":"unc-13 homolog C [Source:HGNC Symbol;Acc:HGNC:23149]","synonyms":"Munc13-3,DKFZp547H074","biotype":"protein_coding","ncbi_id":"440279","summary":null,"start":54012904,"end":54633414,"strand":1,"description":"unc-13 homolog C [Source:HGNC Symbol;Acc:HGNC:23149]"}, {"versioned_ensembl_gene_id":"ENSG00000224976.2","gene_symbol":"PARP4P2","gene_name":"poly(ADP-ribose) polymerase family member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37760]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645771","summary":null,"start":19349137,"end":19407962,"strand":1,"description":"poly(ADP-ribose) polymerase family member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37760]"}, {"versioned_ensembl_gene_id":"ENSG00000249910.3","gene_symbol":"TRIM51CP","gene_name":"tripartite motif-containing 51C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43968]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130105","summary":null,"start":48945694,"end":48951895,"strand":1,"description":"tripartite motif-containing 51C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43968]"}, {"versioned_ensembl_gene_id":"ENSG00000255527.1","gene_symbol":"AC027369.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48907103,"end":48908946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105696.8","gene_symbol":"TMEM59L","gene_name":"transmembrane protein 59 like [Source:HGNC Symbol;Acc:HGNC:13237]","synonyms":"C19orf4,BSMAP","biotype":"protein_coding","ncbi_id":"25789","summary":"This gene encodes a predicted type-I membrane glycoprotein. The encoded protein may play a role in functioning of the central nervous system. [provided by RefSeq, Jul 2008]","start":18607430,"end":18621039,"strand":1,"description":"transmembrane protein 59 like [Source:HGNC Symbol;Acc:HGNC:13237]"}, {"versioned_ensembl_gene_id":"ENSG00000231445.1","gene_symbol":"TIMM8AP1","gene_name":"translocase of inner mitochondrial membrane 8A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17802]","synonyms":"TIMM8AP,DDPP","biotype":"processed_pseudogene","ncbi_id":"399520","summary":null,"start":162077357,"end":162077651,"strand":-1,"description":"translocase of inner mitochondrial membrane 8A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17802]"}, {"versioned_ensembl_gene_id":"ENSG00000270096.1","gene_symbol":"AC078795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169794962,"end":169796213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228030.2","gene_symbol":"AC019084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158719730,"end":158720161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270720.1","gene_symbol":"AC104785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89119284,"end":89119871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261251.1","gene_symbol":"Z97055.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43812456,"end":43817394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167460.14","gene_symbol":"TPM4","gene_name":"tropomyosin 4 [Source:HGNC Symbol;Acc:HGNC:12013]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7171","summary":"This gene encodes a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2009]","start":16067021,"end":16103005,"strand":1,"description":"tropomyosin 4 [Source:HGNC Symbol;Acc:HGNC:12013]"}, {"versioned_ensembl_gene_id":"ENSG00000072163.19","gene_symbol":"LIMS2","gene_name":"LIM zinc finger domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16084]","synonyms":"PINCH2,PINCH-2","biotype":"protein_coding","ncbi_id":"55679","summary":"This gene encodes a member of a small family of focal adhesion proteins which interacts with ILK (integrin-linked kinase), a protein which effects protein-protein interactions with the extraceullar matrix. The encoded protein has five LIM domains, each domain forming two zinc fingers, which permit interactions which regulate cell shape and migration. A pseudogene of this gene is located on chromosome 4. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":127638381,"end":127681786,"strand":-1,"description":"LIM zinc finger domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16084]"}, {"versioned_ensembl_gene_id":"ENSG00000142507.9","gene_symbol":"PSMB6","gene_name":"proteasome subunit beta 6 [Source:HGNC Symbol;Acc:HGNC:9543]","synonyms":"Y,DELTA","biotype":"protein_coding","ncbi_id":"5694","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. The encoded protein is a member of the proteasome B-type family, also known as the T1B family, and is a 20S core beta subunit in the proteasome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":4796144,"end":4798503,"strand":1,"description":"proteasome subunit beta 6 [Source:HGNC Symbol;Acc:HGNC:9543]"}, {"versioned_ensembl_gene_id":"ENSG00000121388.5","gene_symbol":"AL139327.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19185225,"end":19187349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250480.3","gene_symbol":"AC034244.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57120796,"end":57122624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254832.1","gene_symbol":"OR4A40P","gene_name":"olfactory receptor family 4 subfamily A member 40 pseudogene [Source:HGNC Symbol;Acc:HGNC:31259]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390116","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48512273,"end":48513220,"strand":1,"description":"olfactory receptor family 4 subfamily A member 40 pseudogene [Source:HGNC Symbol;Acc:HGNC:31259]"}, {"versioned_ensembl_gene_id":"ENSG00000283328.1","gene_symbol":"AL603764.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":122624524,"end":122624867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241782.1","gene_symbol":"AP002812.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77868722,"end":77869195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185811.17","gene_symbol":"IKZF1","gene_name":"IKAROS family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13176]","synonyms":"ZNFN1A1,PPP1R92,LyF-1,IKAROS,Hs.54452,hIk-1","biotype":"protein_coding","ncbi_id":"10320","summary":"This gene encodes a transcription factor that belongs to the family of zinc-finger DNA-binding proteins associated with chromatin remodeling. The expression of this protein is restricted to the fetal and adult hemo-lymphopoietic system, and it functions as a regulator of lymphocyte differentiation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. Most isoforms share a common C-terminal domain, which contains two zinc finger motifs that are required for hetero- or homo-dimerization, and for interactions with other proteins. The isoforms, however, differ in the number of N-terminal zinc finger motifs that bind DNA and in nuclear localization signal presence, resulting in members with and without DNA-binding properties. Only a few isoforms contain the requisite three or more N-terminal zinc motifs that confer high affinity binding to a specific core DNA sequence element in the promoters of target genes. The non-DNA-binding isoforms are largely found in the cytoplasm, and are thought to function as dominant-negative factors. Overexpression of some dominant-negative isoforms have been associated with B-cell malignancies, such as acute lymphoblastic leukemia (ALL). [provided by RefSeq, May 2014]","start":50304124,"end":50405101,"strand":1,"description":"IKAROS family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13176]"}, {"versioned_ensembl_gene_id":"ENSG00000244187.7","gene_symbol":"TMEM141","gene_name":"transmembrane protein 141 [Source:HGNC Symbol;Acc:HGNC:28211]","synonyms":"MGC14141","biotype":"protein_coding","ncbi_id":"85014","summary":null,"start":136791355,"end":136793257,"strand":1,"description":"transmembrane protein 141 [Source:HGNC Symbol;Acc:HGNC:28211]"}, {"versioned_ensembl_gene_id":"ENSG00000213212.3","gene_symbol":"NCLP1","gene_name":"nucleolin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35472]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100302751","summary":null,"start":136812788,"end":136815536,"strand":-1,"description":"nucleolin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35472]"}, {"versioned_ensembl_gene_id":"ENSG00000255381.1","gene_symbol":"AP001258.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59142121,"end":59142610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259367.1","gene_symbol":"AC087286.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85619623,"end":85670948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162520.14","gene_symbol":"SYNC","gene_name":"syncoilin, intermediate filament protein [Source:HGNC Symbol;Acc:HGNC:28897]","synonyms":"SYNCOILIN,SYNC1","biotype":"protein_coding","ncbi_id":"81493","summary":"This gene encodes a member of the intermediate filament family which contains an N-terminal head domain, followed by a central coiled-coil region and a short C-terminal tail. The protein is highly expressed in skeletal and cardiac muscle. The protein links the dystrophin associated protein complex (DAPC) to desmin filaments in muscle and may have a structural role in striated muscle. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":32680360,"end":32703596,"strand":-1,"description":"syncoilin, intermediate filament protein [Source:HGNC Symbol;Acc:HGNC:28897]"}, {"versioned_ensembl_gene_id":"ENSG00000274665.3","gene_symbol":"PVALB","gene_name":"parvalbumin [Source:HGNC Symbol;Acc:HGNC:9704]","synonyms":"D22S749","biotype":"protein_coding","ncbi_id":"5816","summary":"The protein encoded by this gene is a high affinity calcium ion-binding protein that is structurally and functionally similar to calmodulin and troponin C. The encoded protein is thought to be involved in muscle relaxation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":36800684,"end":36819479,"strand":-1,"description":"parvalbumin [Source:HGNC Symbol;Acc:HGNC:9704]"}, {"versioned_ensembl_gene_id":"ENSG00000266490.1","gene_symbol":"AC127024.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30792372,"end":30792833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074054.17","gene_symbol":"CLASP1","gene_name":"cytoplasmic linker associated protein 1 [Source:HGNC Symbol;Acc:HGNC:17088]","synonyms":"MAST1,KIAA0622","biotype":"protein_coding","ncbi_id":"23332","summary":"CLASPs, such as CLASP1, are nonmotor microtubule-associated proteins that interact with CLIPs (e.g., CLIP170; MIM 179838). CLASP1 is involved in the regulation of microtubule dynamics at the kinetochore and throughout the spindle (Maiato et al., 2003 [PubMed 12837247]).[supplied by OMIM, Mar 2008]","start":121337776,"end":121649587,"strand":-1,"description":"cytoplasmic linker associated protein 1 [Source:HGNC Symbol;Acc:HGNC:17088]"}, {"versioned_ensembl_gene_id":"ENSG00000276250.1","gene_symbol":"AC127024.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30803654,"end":30804077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269028.3","gene_symbol":"MTRNR2L12","gene_name":"MT-RNR2-like 12 [Source:HGNC Symbol;Acc:HGNC:37169]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463498","summary":null,"start":96617188,"end":96618236,"strand":-1,"description":"MT-RNR2-like 12 [Source:HGNC Symbol;Acc:HGNC:37169]"}, {"versioned_ensembl_gene_id":"ENSG00000254966.1","gene_symbol":"AC103974.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18706537,"end":18740568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227243.3","gene_symbol":"SLAMF6P1","gene_name":"SLAM family member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32012]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100862852","summary":null,"start":162445549,"end":162446566,"strand":1,"description":"SLAM family member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32012]"}, {"versioned_ensembl_gene_id":"ENSG00000272106.1","gene_symbol":"AL691432.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1613758,"end":1615795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225351.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994816,"end":29005348,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000089101.17","gene_symbol":"CFAP61","gene_name":"cilia and flagella associated protein 61 [Source:HGNC Symbol;Acc:HGNC:15872]","synonyms":"DKFZP434K156,dJ1002M8.3,CaM-IP3,C20orf26","biotype":"protein_coding","ncbi_id":"26074","summary":null,"start":20052514,"end":20360702,"strand":1,"description":"cilia and flagella associated protein 61 [Source:HGNC Symbol;Acc:HGNC:15872]"}, {"versioned_ensembl_gene_id":"ENSG00000108384.14","gene_symbol":"RAD51C","gene_name":"RAD51 paralog C [Source:HGNC Symbol;Acc:HGNC:9820]","synonyms":"RAD51L2,FANCO","biotype":"protein_coding","ncbi_id":"5889","summary":"This gene is a member of the RAD51 family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51 and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with other RAD51 paralogs and is reported to be important for Holliday junction resolution. Mutations in this gene are associated with Fanconi anemia-like syndrome. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":58692573,"end":58735611,"strand":1,"description":"RAD51 paralog C [Source:HGNC Symbol;Acc:HGNC:9820]"}, {"versioned_ensembl_gene_id":"ENSG00000269609.5","gene_symbol":"RPARP-AS1","gene_name":"RPARP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45238]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100505761","summary":null,"start":102449817,"end":102461106,"strand":1,"description":"RPARP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45238]"}, {"versioned_ensembl_gene_id":"ENSG00000270951.1","gene_symbol":"AL121917.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58876592,"end":58876981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273814.4","gene_symbol":"OCLN","gene_name":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]","synonyms":"PPP1R115","biotype":"protein_coding","ncbi_id":"100506658","summary":"This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]","start":69492007,"end":69556424,"strand":1,"description":"occludin [Source:HGNC Symbol;Acc:HGNC:8104]"}, {"versioned_ensembl_gene_id":"ENSG00000198574.5","gene_symbol":"SH2D1B","gene_name":"SH2 domain containing 1B [Source:HGNC Symbol;Acc:HGNC:30416]","synonyms":"EAT2","biotype":"protein_coding","ncbi_id":"117157","summary":"By binding phosphotyrosines through its free SRC (MIM 190090) homology-2 (SH2) domain, EAT2 regulates signal transduction through receptors expressed on the surface of antigen-presenting cells (Morra et al., 2001 [PubMed 11689425]).[supplied by OMIM, Mar 2008]","start":162395266,"end":162412138,"strand":-1,"description":"SH2 domain containing 1B [Source:HGNC Symbol;Acc:HGNC:30416]"}, {"versioned_ensembl_gene_id":"ENSG00000239439.1","gene_symbol":"RFKP2","gene_name":"riboflavin kinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39182]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132753","summary":null,"start":112030931,"end":112031649,"strand":-1,"description":"riboflavin kinase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39182]"}, {"versioned_ensembl_gene_id":"ENSG00000198033.11","gene_symbol":"TUBA3C","gene_name":"tubulin alpha 3c [Source:HGNC Symbol;Acc:HGNC:12408]","synonyms":"TUBA2,bA408E5.3","biotype":"protein_coding","ncbi_id":"7278","summary":"Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulin. The genes encoding these microtubule constituents are part of the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes and they are highly conserved among and between species. This gene is an alpha tubulin gene that encodes a protein 99% identical to the mouse testis-specific Tuba3 and Tuba7 gene products. This gene is located in the 13q11 region, which is associated with the genetic diseases Clouston hidrotic ectodermal dysplasia and Kabuki syndrome. [provided by RefSeq, Jul 2008]","start":19173770,"end":19181852,"strand":-1,"description":"tubulin alpha 3c [Source:HGNC Symbol;Acc:HGNC:12408]"}, {"versioned_ensembl_gene_id":"ENSG00000237388.2","gene_symbol":"OR4A47","gene_name":"olfactory receptor family 4 subfamily A member 47 [Source:HGNC Symbol;Acc:HGNC:31266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403253","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48488717,"end":48489780,"strand":1,"description":"olfactory receptor family 4 subfamily A member 47 [Source:HGNC Symbol;Acc:HGNC:31266]"}, {"versioned_ensembl_gene_id":"ENSG00000242389.8","gene_symbol":"RBMY1E","gene_name":"RNA binding motif protein, Y-linked, family 1, member E [Source:HGNC Symbol;Acc:HGNC:23916]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378950","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. Multiple copies of this gene are found in the AZFb azoospermia factor region of chromosome Y and the encoded protein is thought to be involved in spermatogenesis. Most copies of this locus are pseudogenes, although six highly similar copies have full-length ORFs and are considered functional. Four functional copies of this gene are found within inverted repeat IR2; two functional copies of this gene are found in palindrome P3, along with two copies of PTPN13-like, Y-linked. [provided by RefSeq, Jul 2008]","start":21903618,"end":21918067,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 1, member E [Source:HGNC Symbol;Acc:HGNC:23916]"}, {"versioned_ensembl_gene_id":"ENSG00000253104.1","gene_symbol":"AC139497.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22139247,"end":22141468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151320.10","gene_symbol":"AKAP6","gene_name":"A-kinase anchoring protein 6 [Source:HGNC Symbol;Acc:HGNC:376]","synonyms":"PRKA6,mAKAP,KIAA0311,AKAP100,ADAP6","biotype":"protein_coding","ncbi_id":"9472","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is highly expressed in various brain regions and cardiac and skeletal muscle. It is specifically localized to the sarcoplasmic reticulum and nuclear membrane, and is involved in anchoring PKA to the nuclear membrane or sarcoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":32329273,"end":32837681,"strand":1,"description":"A-kinase anchoring protein 6 [Source:HGNC Symbol;Acc:HGNC:376]"}, {"versioned_ensembl_gene_id":"ENSG00000258580.1","gene_symbol":"AL136298.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32373337,"end":32417974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246334.2","gene_symbol":"PRR7-AS1","gene_name":"PRR7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27961]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"340037","summary":null,"start":177438503,"end":177447699,"strand":-1,"description":"PRR7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27961]"}, {"versioned_ensembl_gene_id":"ENSG00000226691.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32929849,"end":32929923,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000229416.1","gene_symbol":"USP9YP8","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38424]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421219","summary":null,"start":21677246,"end":21681118,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38424]"}, {"versioned_ensembl_gene_id":"ENSG00000232057.1","gene_symbol":"AC093390.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1824412,"end":1828667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225131.2","gene_symbol":"PSME2P2","gene_name":"proteasome activator subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30160]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338099","summary":null,"start":48771128,"end":48771827,"strand":1,"description":"proteasome activator subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30160]"}, {"versioned_ensembl_gene_id":"ENSG00000226396.1","gene_symbol":"AL031727.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19608114,"end":19608568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196724.12","gene_symbol":"ZNF418","gene_name":"zinc finger protein 418 [Source:HGNC Symbol;Acc:HGNC:20647]","synonyms":"KIAA1956,FLJ31551","biotype":"protein_coding","ncbi_id":"147686","summary":null,"start":57921884,"end":57935393,"strand":-1,"description":"zinc finger protein 418 [Source:HGNC Symbol;Acc:HGNC:20647]"}, {"versioned_ensembl_gene_id":"ENSG00000120471.15","gene_symbol":"TP53AIP1","gene_name":"tumor protein p53 regulated apoptosis inducing protein 1 [Source:HGNC Symbol;Acc:HGNC:29984]","synonyms":"p53AIP1","biotype":"protein_coding","ncbi_id":"63970","summary":"This gene is specifically expressed in the thymus, and encodes a protein that is localized to the mitochondrion. The expression of this gene is inducible by p53, and it is thought to play an important role in mediating p53-dependent apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":128934731,"end":128943399,"strand":-1,"description":"tumor protein p53 regulated apoptosis inducing protein 1 [Source:HGNC Symbol;Acc:HGNC:29984]"}, {"versioned_ensembl_gene_id":"ENSG00000227043.1","gene_symbol":"LINC01682","gene_name":"long intergenic non-protein coding RNA 1682 [Source:HGNC Symbol;Acc:HGNC:52470]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927504","summary":null,"start":229875550,"end":229885752,"strand":-1,"description":"long intergenic non-protein coding RNA 1682 [Source:HGNC Symbol;Acc:HGNC:52470]"}, {"versioned_ensembl_gene_id":"ENSG00000258651.1","gene_symbol":"SEC23A-AS1","gene_name":"SEC23A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53213]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370458","summary":null,"start":39103140,"end":39103812,"strand":1,"description":"SEC23A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53213]"}, {"versioned_ensembl_gene_id":"ENSG00000162745.10","gene_symbol":"OLFML2B","gene_name":"olfactomedin like 2B [Source:HGNC Symbol;Acc:HGNC:24558]","synonyms":"DKFZP586L151","biotype":"protein_coding","ncbi_id":"25903","summary":"This gene encodes an olfactomedin domain-containing protein. Most olfactomedin domain-containing proteins are secreted glycoproteins. [provided by RefSeq, Dec 2016]","start":161983192,"end":162023854,"strand":-1,"description":"olfactomedin like 2B [Source:HGNC Symbol;Acc:HGNC:24558]"}, {"versioned_ensembl_gene_id":"ENSG00000225984.1","gene_symbol":"HMGB1P26","gene_name":"high mobility group box 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645201","summary":null,"start":229705234,"end":229705861,"strand":-1,"description":"high mobility group box 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39117]"}, {"versioned_ensembl_gene_id":"ENSG00000213028.3","gene_symbol":"AL354983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":229688999,"end":229689904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173436.13","gene_symbol":"MINOS1","gene_name":"mitochondrial inner membrane organizing system 1 [Source:HGNC Symbol;Acc:HGNC:32068]","synonyms":"MIO10,Mic10,FLJ36999,C1orf151,RP5-1056L3.2","biotype":"protein_coding","ncbi_id":"440574","summary":null,"start":19596977,"end":19629821,"strand":1,"description":"mitochondrial inner membrane organizing system 1 [Source:HGNC Symbol;Acc:HGNC:32068]"}, {"versioned_ensembl_gene_id":"ENSG00000281507.1","gene_symbol":"AC136352.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21328492,"end":21343937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273213.1","gene_symbol":"AC239798.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143904301,"end":143905964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275038.1","gene_symbol":"AC091980.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":171305981,"end":171308755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116678.19","gene_symbol":"LEPR","gene_name":"leptin receptor [Source:HGNC Symbol;Acc:HGNC:6554]","synonyms":"CD295,OBR","biotype":"protein_coding","ncbi_id":"3953","summary":"The protein encoded by this gene belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins. This protein is a receptor for leptin (an adipocyte-specific hormone that regulates body weight), and is involved in the regulation of fat metabolism, as well as in a novel hematopoietic pathway that is required for normal lymphopoiesis. Mutations in this gene have been associated with obesity and pituitary dysfunction. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. It is noteworthy that this gene and LEPROT gene (GeneID:54741) share the same promoter and the first 2 exons, however, encode distinct proteins (PMID:9207021).[provided by RefSeq, Nov 2010]","start":65420652,"end":65641559,"strand":1,"description":"leptin receptor [Source:HGNC Symbol;Acc:HGNC:6554]"}, {"versioned_ensembl_gene_id":"ENSG00000225956.1","gene_symbol":"AL050320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13244064,"end":13245369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236149.9","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"EST123147,ABC50","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30561217,"end":30587022,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000173221.13","gene_symbol":"GLRX","gene_name":"glutaredoxin [Source:HGNC Symbol;Acc:HGNC:4330]","synonyms":"GRX1,GRX","biotype":"protein_coding","ncbi_id":"2745","summary":"This gene encodes a member of the glutaredoxin family. The encoded protein is a cytoplasmic enzyme catalyzing the reversible reduction of glutathione-protein mixed disulfides. This enzyme highly contributes to the antioxidant defense system. It is crucial for several signalling pathways by controlling the S-glutathionylation status of signalling mediators. It is involved in beta-amyloid toxicity and Alzheimer's disease. Multiple alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Aug 2011]","start":95751319,"end":95823005,"strand":-1,"description":"glutaredoxin [Source:HGNC Symbol;Acc:HGNC:4330]"}, {"versioned_ensembl_gene_id":"ENSG00000186010.18","gene_symbol":"NDUFA13","gene_name":"NADH:ubiquinone oxidoreductase subunit A13 [Source:HGNC Symbol;Acc:HGNC:17194]","synonyms":"GRIM19,GRIM-19,CGI-39,CDA016,B16.6","biotype":"protein_coding","ncbi_id":"51079","summary":"This gene encodes a subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), which functions in the transfer of electrons from NADH to the respiratory chain. The protein is required for complex I assembly and electron transfer activity. The protein binds the signal transducers and activators of transcription 3 (STAT3) transcription factor, and can function as a tumor suppressor. The human protein purified from mitochondria migrates at approximately 16 kDa. Transcripts originating from an upstream promoter and capable of expressing a protein with a longer N-terminus have been found, but their biological validity has not been determined. [provided by RefSeq, Oct 2009]","start":19515736,"end":19529054,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A13 [Source:HGNC Symbol;Acc:HGNC:17194]"}, {"versioned_ensembl_gene_id":"ENSG00000100139.13","gene_symbol":"MICALL1","gene_name":"MICAL like 1 [Source:HGNC Symbol;Acc:HGNC:29804]","synonyms":"MIRAB13,MICAL-L1,KIAA1668","biotype":"protein_coding","ncbi_id":"85377","summary":null,"start":37905657,"end":37942822,"strand":1,"description":"MICAL like 1 [Source:HGNC Symbol;Acc:HGNC:29804]"}, {"versioned_ensembl_gene_id":"ENSG00000106868.16","gene_symbol":"SUSD1","gene_name":"sushi domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25413]","synonyms":"DKFZP761E1824","biotype":"protein_coding","ncbi_id":"64420","summary":null,"start":112040785,"end":112175408,"strand":-1,"description":"sushi domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25413]"}, {"versioned_ensembl_gene_id":"ENSG00000231720.1","gene_symbol":"AL353747.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167237508,"end":167240480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166917.10","gene_symbol":"MIR202HG","gene_name":"MIR202 host gene [Source:HGNC Symbol;Acc:HGNC:49402]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927671","summary":null,"start":133246478,"end":133247891,"strand":-1,"description":"MIR202 host gene [Source:HGNC Symbol;Acc:HGNC:49402]"}, {"versioned_ensembl_gene_id":"ENSG00000171794.3","gene_symbol":"UTF1","gene_name":"undifferentiated embryonic cell transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8433","summary":"The protein encoded by this gene is a leucine zipper-containing transcriptional coactivator that may link the upstream activator ATF2 with the basal transcription complex. The encoded protein is closely associated with chromatin and is required for the proper differentiation of embryonic carcinoma and embryonic stem cells. Found nearly exclusively in pluripotent cells, this protein can also serve as a transcriptional repressor. [provided by RefSeq, Nov 2015]","start":133230274,"end":133231558,"strand":1,"description":"undifferentiated embryonic cell transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12634]"}, {"versioned_ensembl_gene_id":"ENSG00000181790.10","gene_symbol":"ADGRB1","gene_name":"adhesion G protein-coupled receptor B1 [Source:HGNC Symbol;Acc:HGNC:943]","synonyms":"BAI1","biotype":"protein_coding","ncbi_id":"575","summary":"Angiogenesis is controlled by a local balance between stimulators and inhibitors of new vessel growth and is suppressed under normal physiologic conditions. Angiogenesis has been shown to be essential for growth and metastasis of solid tumors. In order to obtain blood supply for their growth, tumor cells are potently angiogenic and attract new vessels as results of increased secretion of inducers and decreased production of endogenous negative regulators. BAI1 contains at least one 'functional' p53-binding site within an intron, and its expression has been shown to be induced by wildtype p53. There are two other brain-specific angiogenesis inhibitor genes, designated BAI2 and BAI3 which along with BAI1 have similar tissue specificities and structures, however only BAI1 is transcriptionally regulated by p53. BAI1 is postulated to be a member of the secretin receptor family, an inhibitor of angiogenesis and a growth suppressor of glioblastomas [provided by RefSeq, Jul 2008]","start":142449430,"end":142545009,"strand":1,"description":"adhesion G protein-coupled receptor B1 [Source:HGNC Symbol;Acc:HGNC:943]"}, {"versioned_ensembl_gene_id":"ENSG00000234678.1","gene_symbol":"ELF3-AS1","gene_name":"ELF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40211]","synonyms":"ENST00000415582","biotype":"antisense_RNA","ncbi_id":"102723465","summary":null,"start":202000094,"end":202010353,"strand":-1,"description":"ELF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40211]"}, {"versioned_ensembl_gene_id":"ENSG00000183647.10","gene_symbol":"ZNF530","gene_name":"zinc finger protein 530 [Source:HGNC Symbol;Acc:HGNC:29297]","synonyms":"KIAA1508","biotype":"protein_coding","ncbi_id":"348327","summary":null,"start":57599885,"end":57612722,"strand":1,"description":"zinc finger protein 530 [Source:HGNC Symbol;Acc:HGNC:29297]"}, {"versioned_ensembl_gene_id":"ENSG00000164414.17","gene_symbol":"SLC35A1","gene_name":"solute carrier family 35 member A1 [Source:HGNC Symbol;Acc:HGNC:11021]","synonyms":"hCST,CMPST","biotype":"protein_coding","ncbi_id":"10559","summary":"The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]","start":87470623,"end":87512336,"strand":1,"description":"solute carrier family 35 member A1 [Source:HGNC Symbol;Acc:HGNC:11021]"}, {"versioned_ensembl_gene_id":"ENSG00000232267.1","gene_symbol":"ACTR3P2","gene_name":"ACTR3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129013","summary":null,"start":68771322,"end":68772578,"strand":1,"description":"ACTR3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38676]"}, {"versioned_ensembl_gene_id":"ENSG00000224246.2","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":30921066,"end":30921888,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000138756.17","gene_symbol":"BMP2K","gene_name":"BMP2 inducible kinase [Source:HGNC Symbol;Acc:HGNC:18041]","synonyms":"DKFZp434K0614,BIKe","biotype":"protein_coding","ncbi_id":"55589","summary":"This gene is the human homolog of mouse BMP-2-inducible kinase. Bone morphogenic proteins (BMPs) play a key role in skeletal development and patterning. Expression of the mouse gene is increased during BMP-2 induced differentiation and the gene product is a putative serine/threonine protein kinase containing a nuclear localization signal. Therefore, the protein encoded by this human homolog is thought to be a protein kinase with a putative regulatory role in attenuating the program of osteoblast differentiation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":78776342,"end":78916372,"strand":1,"description":"BMP2 inducible kinase [Source:HGNC Symbol;Acc:HGNC:18041]"}, {"versioned_ensembl_gene_id":"ENSG00000260873.6","gene_symbol":"SNTB2","gene_name":"syntrophin beta 2 [Source:HGNC Symbol;Acc:HGNC:11169]","synonyms":"EST25263,D16S2531E,SNTL,SNT3,SNT2B2","biotype":"protein_coding","ncbi_id":"6645","summary":"Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]","start":69187122,"end":69187739,"strand":1,"description":"syntrophin beta 2 [Source:HGNC Symbol;Acc:HGNC:11169]"}, {"versioned_ensembl_gene_id":"ENSG00000228906.1","gene_symbol":"AL353804.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73948973,"end":73949558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083814.13","gene_symbol":"ZNF671","gene_name":"zinc finger protein 671 [Source:HGNC Symbol;Acc:HGNC:26279]","synonyms":"FLJ23506","biotype":"protein_coding","ncbi_id":"79891","summary":null,"start":57719751,"end":57727624,"strand":-1,"description":"zinc finger protein 671 [Source:HGNC Symbol;Acc:HGNC:26279]"}, {"versioned_ensembl_gene_id":"ENSG00000241216.1","gene_symbol":"SNAPC5P1","gene_name":"small nuclear RNA activating complex polypeptide 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38667]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100750245","summary":null,"start":6347081,"end":6347381,"strand":-1,"description":"small nuclear RNA activating complex polypeptide 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38667]"}, {"versioned_ensembl_gene_id":"ENSG00000267282.1","gene_symbol":"AC011481.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44882027,"end":44890876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271199.1","gene_symbol":"AL353804.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":73958059,"end":73969485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257860.5","gene_symbol":"AC068643.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103151842,"end":103168309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083817.8","gene_symbol":"ZNF416","gene_name":"zinc finger protein 416 [Source:HGNC Symbol;Acc:HGNC:20645]","synonyms":"FLJ20557","biotype":"protein_coding","ncbi_id":"55659","summary":null,"start":57571566,"end":57578927,"strand":-1,"description":"zinc finger protein 416 [Source:HGNC Symbol;Acc:HGNC:20645]"}, {"versioned_ensembl_gene_id":"ENSG00000259736.1","gene_symbol":"CRTC3-AS1","gene_name":"CRTC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51433]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926895","summary":null,"start":90620007,"end":90717141,"strand":-1,"description":"CRTC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51433]"}, {"versioned_ensembl_gene_id":"ENSG00000275461.1","gene_symbol":"AC084768.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5716584,"end":5716804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061936.9","gene_symbol":"SFSWAP","gene_name":"splicing factor SWAP homolog [Source:HGNC Symbol;Acc:HGNC:10790]","synonyms":"SFRS8,SWAP","biotype":"protein_coding","ncbi_id":"6433","summary":"This gene encodes a human homolog of Drosophila splicing regulatory protein. This gene autoregulates its expression by control of splicing of its first two introns. In addition, it also regulates the splicing of fibronectin and CD45 genes. Two transcript variants encoding different isoforms have been identified. [provided by RefSeq, May 2012]","start":131711081,"end":131799737,"strand":1,"description":"splicing factor SWAP homolog [Source:HGNC Symbol;Acc:HGNC:10790]"}, {"versioned_ensembl_gene_id":"ENSG00000237135.1","gene_symbol":"DDX10P1","gene_name":"DEAD-box helicase 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421371","summary":null,"start":30919012,"end":30921235,"strand":-1,"description":"DEAD-box helicase 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44960]"}, {"versioned_ensembl_gene_id":"ENSG00000248727.5","gene_symbol":"LINC01948","gene_name":"long intergenic non-protein coding RNA 1948 [Source:HGNC Symbol;Acc:HGNC:52772]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467147","summary":null,"start":56457795,"end":56481946,"strand":-1,"description":"long intergenic non-protein coding RNA 1948 [Source:HGNC Symbol;Acc:HGNC:52772]"}, {"versioned_ensembl_gene_id":"ENSG00000235356.1","gene_symbol":"AL592466.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65313785,"end":65314970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227761.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31621198,"end":31634883,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000183621.15","gene_symbol":"ZNF438","gene_name":"zinc finger protein 438 [Source:HGNC Symbol;Acc:HGNC:21029]","synonyms":"bA330O11.1","biotype":"protein_coding","ncbi_id":"220929","summary":null,"start":30820207,"end":31031937,"strand":-1,"description":"zinc finger protein 438 [Source:HGNC Symbol;Acc:HGNC:21029]"}, {"versioned_ensembl_gene_id":"ENSG00000119711.12","gene_symbol":"ALDH6A1","gene_name":"aldehyde dehydrogenase 6 family member A1 [Source:HGNC Symbol;Acc:HGNC:7179]","synonyms":"MMSDH","biotype":"protein_coding","ncbi_id":"4329","summary":"This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":74056850,"end":74084493,"strand":-1,"description":"aldehyde dehydrogenase 6 family member A1 [Source:HGNC Symbol;Acc:HGNC:7179]"}, {"versioned_ensembl_gene_id":"ENSG00000223850.1","gene_symbol":"MYCNUT","gene_name":"MYCN upstream transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32684]","synonyms":"MYCNUN,lncUSMycN","biotype":"lincRNA","ncbi_id":"103752554","summary":null,"start":15920399,"end":15936017,"strand":1,"description":"MYCN upstream transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32684]"}, {"versioned_ensembl_gene_id":"ENSG00000282268.1","gene_symbol":"IGHD2OR15-2B","gene_name":"immunoglobulin heavy diversity 2/OR15-2B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5494]","synonyms":"IGHD2OR152B,IGHD2/OR15-2B","biotype":"IG_D_gene","ncbi_id":"28332","summary":null,"start":21015048,"end":21015078,"strand":-1,"description":"immunoglobulin heavy diversity 2/OR15-2B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5494]"}, {"versioned_ensembl_gene_id":"ENSG00000282003.1","gene_symbol":"TUBGCP3","gene_name":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]","synonyms":"Spc98p,SPBC98,GCP3","biotype":"protein_coding","ncbi_id":"10426","summary":null,"start":112468853,"end":112488558,"strand":-1,"description":"tubulin gamma complex associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18598]"}, {"versioned_ensembl_gene_id":"ENSG00000134323.11","gene_symbol":"MYCN","gene_name":"MYCN proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7559]","synonyms":"NMYC,N-myc,MYCNOT,bHLHe37","biotype":"protein_coding","ncbi_id":"4613","summary":"This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":15940564,"end":15947007,"strand":1,"description":"MYCN proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7559]"}, {"versioned_ensembl_gene_id":"ENSG00000272606.1","gene_symbol":"AC015982.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55617909,"end":55618373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275052.4","gene_symbol":"PPP4R3B","gene_name":"protein phosphatase 4 regulatory subunit 3B [Source:HGNC Symbol;Acc:HGNC:29267]","synonyms":"SMEK2,PSY2,KIAA1387,FLJ31474,FLFL2","biotype":"protein_coding","ncbi_id":"57223","summary":null,"start":55547292,"end":55618880,"strand":-1,"description":"protein phosphatase 4 regulatory subunit 3B [Source:HGNC Symbol;Acc:HGNC:29267]"}, {"versioned_ensembl_gene_id":"ENSG00000265531.3","gene_symbol":"FCGR1CP","gene_name":"Fc fragment of IgG receptor Ic, pseudogene [Source:HGNC Symbol;Acc:HGNC:3615]","synonyms":"FCGR1C,CD64c","biotype":"unprocessed_pseudogene","ncbi_id":"100132417","summary":"The gene represents one of three related immunoglobulin gamma Fc receptor genes located on chromosome 1. This family member lacks the transmembrane and coiled-coiled domains found in other family members and is thought to be a pseudogene of Fc-gamma-receptor 1A. [provided by RefSeq, Apr 2009]","start":143874793,"end":143883575,"strand":1,"description":"Fc fragment of IgG receptor Ic, pseudogene [Source:HGNC Symbol;Acc:HGNC:3615]"}, {"versioned_ensembl_gene_id":"ENSG00000283586.1","gene_symbol":"AC097495.1","gene_name":null,"synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":null,"summary":null,"start":68921248,"end":68926834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249276.1","gene_symbol":"AC104119.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43874367,"end":43886628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237836.5","gene_symbol":"PHKA2-AS1","gene_name":"PHKA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44110]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132163","summary":null,"start":18890296,"end":18894497,"strand":1,"description":"PHKA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44110]"}, {"versioned_ensembl_gene_id":"ENSG00000203818.7","gene_symbol":"HIST2H3PS2","gene_name":"histone cluster 2 H3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32060]","synonyms":"p06","biotype":"protein_coding","ncbi_id":"440686","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a member of the H3 family, but is found outside of the histone cluster. There is evidence that it is transcribed and has an intact CDS, but residue changes in the protein suggest that it may be on its way to becoming a psuedogene. [provided by RefSeq, Aug 2019]","start":143905556,"end":143905966,"strand":-1,"description":"histone cluster 2 H3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32060]"}, {"versioned_ensembl_gene_id":"ENSG00000227204.1","gene_symbol":"RBMY2JP","gene_name":"RNA binding motif protein, Y-linked, family 2, member J pseudogene [Source:HGNC Symbol;Acc:HGNC:23918]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378955","summary":null,"start":8127130,"end":8144203,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member J pseudogene [Source:HGNC Symbol;Acc:HGNC:23918]"}, {"versioned_ensembl_gene_id":"ENSG00000282782.1","gene_symbol":"CYP4F34P","gene_name":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]","synonyms":"CYP4F-se7[6:7:8]","biotype":"unprocessed_pseudogene","ncbi_id":"100422247","summary":null,"start":18741730,"end":18742718,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:39953]"}, {"versioned_ensembl_gene_id":"ENSG00000233041.8","gene_symbol":"PHGR1","gene_name":"proline, histidine and glycine rich 1 [Source:HGNC Symbol;Acc:HGNC:37226]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644844","summary":null,"start":40351033,"end":40356434,"strand":1,"description":"proline, histidine and glycine rich 1 [Source:HGNC Symbol;Acc:HGNC:37226]"}, {"versioned_ensembl_gene_id":"ENSG00000164438.5","gene_symbol":"TLX3","gene_name":"T-cell leukemia homeobox 3 [Source:HGNC Symbol;Acc:HGNC:13532]","synonyms":"HOX11L2,RNX","biotype":"protein_coding","ncbi_id":"30012","summary":"The protein encoded by this gene is an orphan homeobox protein that encodes a DNA-binding nuclear transcription factor. A translocation [t(5;14)(q35;q32)] involving this gene is associated with T-cell acute lymphoblastic leukemia (T-ALL) in children and young adults. [provided by RefSeq, Nov 2015]","start":171309284,"end":171312134,"strand":1,"description":"T-cell leukemia homeobox 3 [Source:HGNC Symbol;Acc:HGNC:13532]"}, {"versioned_ensembl_gene_id":"ENSG00000044446.11","gene_symbol":"PHKA2","gene_name":"phosphorylase kinase regulatory subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:8926]","synonyms":"PYK,PHK","biotype":"protein_coding","ncbi_id":"5256","summary":"Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, which are encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9A, also known as X-linked liver glycogenosis. Alternatively spliced transcript variants have been reported, but the full-length nature of these variants has not been determined.[provided by RefSeq, Feb 2010]","start":18892300,"end":18984598,"strand":-1,"description":"phosphorylase kinase regulatory subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:8926]"}, {"versioned_ensembl_gene_id":"ENSG00000173110.7","gene_symbol":"HSPA6","gene_name":"heat shock protein family A (Hsp70) member 6 [Source:HGNC Symbol;Acc:HGNC:5239]","synonyms":"HSP70B'","biotype":"protein_coding","ncbi_id":"3310","summary":null,"start":161524540,"end":161526910,"strand":1,"description":"heat shock protein family A (Hsp70) member 6 [Source:HGNC Symbol;Acc:HGNC:5239]"}, {"versioned_ensembl_gene_id":"ENSG00000230186.3","gene_symbol":"AC246680.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143905487,"end":143934776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267234.1","gene_symbol":"AC092067.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19401979,"end":19402603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229407.5","gene_symbol":"AL359853.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179816184,"end":179818191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282677.1","gene_symbol":"SNX18P26","gene_name":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419038","summary":null,"start":18807279,"end":18808018,"strand":-1,"description":"sorting nexin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39634]"}, {"versioned_ensembl_gene_id":"ENSG00000273112.1","gene_symbol":"AL590385.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":161513176,"end":161605099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143340.6","gene_symbol":"FAM163A","gene_name":"family with sequence similarity 163 member A [Source:HGNC Symbol;Acc:HGNC:28274]","synonyms":"NDSP,MGC16664,C1orf76","biotype":"protein_coding","ncbi_id":"148753","summary":null,"start":179743163,"end":179816198,"strand":1,"description":"family with sequence similarity 163 member A [Source:HGNC Symbol;Acc:HGNC:28274]"}, {"versioned_ensembl_gene_id":"ENSG00000187791.12","gene_symbol":"FAM205C","gene_name":"family with sequence similarity 205 member C [Source:HGNC Symbol;Acc:HGNC:42673]","synonyms":"FAM205CP","biotype":"protein_coding","ncbi_id":"100129969","summary":null,"start":34889064,"end":34895778,"strand":-1,"description":"family with sequence similarity 205 member C [Source:HGNC Symbol;Acc:HGNC:42673]"}, {"versioned_ensembl_gene_id":"ENSG00000213393.5","gene_symbol":"AC091980.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171345343,"end":171345630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224203.2","gene_symbol":"RPS23P10","gene_name":"ribosomal protein S23 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48342]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419471","summary":null,"start":161536571,"end":161538158,"strand":-1,"description":"ribosomal protein S23 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48342]"}, {"versioned_ensembl_gene_id":"ENSG00000259368.1","gene_symbol":"AC013356.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40368925,"end":40369640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140323.5","gene_symbol":"DISP2","gene_name":"dispatched RND transporter family member 2 [Source:HGNC Symbol;Acc:HGNC:19712]","synonyms":"HsT16908,DISPB,C15orf36,LINC00594,KIAA1742","biotype":"protein_coding","ncbi_id":"85455","summary":"This gene is one of two human homologs of a segment-polarity gene known as dispatched identified in Drosophila. The product of this gene may be required for normal Hedgehog (Hh) signaling during embryonic pattern formation. [provided by RefSeq, Jan 2017]","start":40358235,"end":40378639,"strand":1,"description":"dispatched RND transporter family member 2 [Source:HGNC Symbol;Acc:HGNC:19712]"}, {"versioned_ensembl_gene_id":"ENSG00000254012.1","gene_symbol":"RPL10P8","gene_name":"ribosomal protein L10 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644937","summary":null,"start":171366299,"end":171366611,"strand":1,"description":"ribosomal protein L10 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52344]"}, {"versioned_ensembl_gene_id":"ENSG00000095015.5","gene_symbol":"MAP3K1","gene_name":"mitogen-activated protein kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6848]","synonyms":"MEKK1,MEKK,MAPKKK1","biotype":"protein_coding","ncbi_id":"4214","summary":"The protein encoded by this gene is a serine/threonine kinase and is part of some signal transduction cascades, including the ERK and JNK kinase pathways as well as the NF-kappa-B pathway. The encoded protein is activated by autophosphorylation and requires magnesium as a cofactor in phosphorylating other proteins. This protein has E3 ligase activity conferred by a plant homeodomain (PHD) in its N-terminus and phospho-kinase activity conferred by a kinase domain in its C-terminus. [provided by RefSeq, Mar 2012]","start":56815574,"end":56896152,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6848]"}, {"versioned_ensembl_gene_id":"ENSG00000074695.5","gene_symbol":"LMAN1","gene_name":"lectin, mannose binding 1 [Source:HGNC Symbol;Acc:HGNC:6631]","synonyms":"ERGIC-53,MR60,MCFD1,gp58,FMFD1,F5F8D,ERGIC53","biotype":"protein_coding","ncbi_id":"3998","summary":"The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH-sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015]","start":59327823,"end":59359962,"strand":-1,"description":"lectin, mannose binding 1 [Source:HGNC Symbol;Acc:HGNC:6631]"}, {"versioned_ensembl_gene_id":"ENSG00000254256.1","gene_symbol":"RPSAP71","gene_name":"ribosomal protein SA pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:51924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075249","summary":null,"start":171365595,"end":171367693,"strand":1,"description":"ribosomal protein SA pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:51924]"}, {"versioned_ensembl_gene_id":"ENSG00000143226.13","gene_symbol":"FCGR2A","gene_name":"Fc fragment of IgG receptor IIa [Source:HGNC Symbol;Acc:HGNC:3616]","synonyms":"IGFR2,FCGR2A1,FCGR2,FCG2,CDw32,CD32A,CD32","biotype":"protein_coding","ncbi_id":"2212","summary":"This gene encodes one member of a family of immunoglobulin Fc receptor genes found on the surface of many immune response cells. The protein encoded by this gene is a cell surface receptor found on phagocytic cells such as macrophages and neutrophils, and is involved in the process of phagocytosis and clearing of immune complexes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008]","start":161505430,"end":161524013,"strand":1,"description":"Fc fragment of IgG receptor IIa [Source:HGNC Symbol;Acc:HGNC:3616]"}, {"versioned_ensembl_gene_id":"ENSG00000255546.1","gene_symbol":"AP001973.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127021754,"end":127053553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165025.14","gene_symbol":"SYK","gene_name":"spleen associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11491]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6850","summary":"This gene encodes a member of the family of non-receptor type Tyr protein kinases. This protein is widely expressed in hematopoietic cells and is involved in coupling activated immunoreceptors to downstream signaling events that mediate diverse cellular responses, including proliferation, differentiation, and phagocytosis. It is thought to be a modulator of epithelial cell growth and a potential tumour suppressor in human breast carcinomas. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":90801787,"end":90898549,"strand":1,"description":"spleen associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11491]"}, {"versioned_ensembl_gene_id":"ENSG00000279717.1","gene_symbol":"AC005336.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15904556,"end":15907234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255087.2","gene_symbol":"AP001993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127067002,"end":127101320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070193.4","gene_symbol":"FGF10","gene_name":"fibroblast growth factor 10 [Source:HGNC Symbol;Acc:HGNC:3666]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2255","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This gene is also implicated to be a primary factor in the process of wound healing. [provided by RefSeq, Jul 2008]","start":44303544,"end":44389706,"strand":-1,"description":"fibroblast growth factor 10 [Source:HGNC Symbol;Acc:HGNC:3666]"}, {"versioned_ensembl_gene_id":"ENSG00000278344.1","gene_symbol":"AC063943.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120500735,"end":120501090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186723.4","gene_symbol":"OR10H1","gene_name":"olfactory receptor family 10 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8172]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26539","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15804549,"end":15815664,"strand":-1,"description":"olfactory receptor family 10 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8172]"}, {"versioned_ensembl_gene_id":"ENSG00000155975.9","gene_symbol":"VPS37A","gene_name":"VPS37A, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:24928]","synonyms":"SPG53,PQBP2,HCRP1,FLJ32642","biotype":"protein_coding","ncbi_id":"137492","summary":"This gene belongs to the VPS37 family, and encodes a component of the ESCRT-I (endosomal sorting complex required for transport I) protein complex, required for the sorting of ubiquitinated transmembrane proteins into internal vesicles of multivesicular bodies. Expression of this gene is downregulated in hepatocellular carcinoma, and mutations in this gene are associated with autosomal recessive spastic paraplegia-53. A related pseudogene has been identified on chromosome 5. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]","start":17246571,"end":17302427,"strand":1,"description":"VPS37A, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:24928]"}, {"versioned_ensembl_gene_id":"ENSG00000268518.1","gene_symbol":"AC020909.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50486810,"end":50487638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267594.5","gene_symbol":"CYP4F24P","gene_name":"cytochrome P450 family 4 subfamily F member 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:39945]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"388514","summary":null,"start":15760241,"end":15779909,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:39945]"}, {"versioned_ensembl_gene_id":"ENSG00000237176.4","gene_symbol":"AC079905.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59812102,"end":59812576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268854.1","gene_symbol":"AC020909.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50480119,"end":50483351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257294.2","gene_symbol":"AC080011.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60092864,"end":60096071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282636.1","gene_symbol":"AC023315.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36981999,"end":36982254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171483.13","gene_symbol":"SSX6","gene_name":"SSX family member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:19652]","synonyms":"SSXP2,SSX6P,psiSSX2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"280657","summary":"This gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene is classified as a pseudogene because a splice donor in the 3' UTR has changed compared to other family members, rendering the transcript a candidate for nonsense-mediated mRNA decay (NMD). [provided by RefSeq, Aug 2009]","start":48107992,"end":48120210,"strand":1,"description":"SSX family member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:19652]"}, {"versioned_ensembl_gene_id":"ENSG00000258184.1","gene_symbol":"AC087883.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60215994,"end":60216384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161671.16","gene_symbol":"EMC10","gene_name":"ER membrane protein complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:27609]","synonyms":"HSM1,C19orf63,INM02,HSS1","biotype":"protein_coding","ncbi_id":"284361","summary":null,"start":50476400,"end":50490870,"strand":1,"description":"ER membrane protein complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:27609]"}, {"versioned_ensembl_gene_id":"ENSG00000267695.1","gene_symbol":"AC105227.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50302190,"end":50313595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146233.7","gene_symbol":"CYP39A1","gene_name":"cytochrome P450 family 39 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:17449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51302","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein is involved in the conversion of cholesterol to bile acids. Its substrates include the oxysterols 25-hydroxycholesterol, 27-hydroxycholesterol and 24-hydroxycholesterol. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":46549580,"end":46652830,"strand":-1,"description":"cytochrome P450 family 39 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:17449]"}, {"versioned_ensembl_gene_id":"ENSG00000143632.14","gene_symbol":"ACTA1","gene_name":"actin, alpha 1, skeletal muscle [Source:HGNC Symbol;Acc:HGNC:129]","synonyms":"NEM3,ACTA","biotype":"protein_coding","ncbi_id":"58","summary":"The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019]","start":229431245,"end":229434098,"strand":-1,"description":"actin, alpha 1, skeletal muscle [Source:HGNC Symbol;Acc:HGNC:129]"}, {"versioned_ensembl_gene_id":"ENSG00000248464.1","gene_symbol":"FGF10-AS1","gene_name":"FGF10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49382]","synonyms":"RP11-473L15.2","biotype":"antisense_RNA","ncbi_id":"101927075","summary":null,"start":44388732,"end":44413989,"strand":1,"description":"FGF10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49382]"}, {"versioned_ensembl_gene_id":"ENSG00000239614.1","gene_symbol":"HMGN1P7","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129555","summary":null,"start":93988634,"end":93988946,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39350]"}, {"versioned_ensembl_gene_id":"ENSG00000267558.2","gene_symbol":"AC087685.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45788530,"end":45788670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267235.2","gene_symbol":"ZNF861P","gene_name":"zinc finger protein 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:34514]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100302737","summary":null,"start":15821796,"end":15823797,"strand":-1,"description":"zinc finger protein 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:34514]"}, {"versioned_ensembl_gene_id":"ENSG00000178694.9","gene_symbol":"NSUN3","gene_name":"NOP2/Sun RNA methyltransferase family member 3 [Source:HGNC Symbol;Acc:HGNC:26208]","synonyms":"FLJ22609","biotype":"protein_coding","ncbi_id":"63899","summary":null,"start":94062916,"end":94128545,"strand":1,"description":"NOP2/Sun RNA methyltransferase family member 3 [Source:HGNC Symbol;Acc:HGNC:26208]"}, {"versioned_ensembl_gene_id":"ENSG00000268673.3","gene_symbol":"AC004597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15760375,"end":15770828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248753.1","gene_symbol":"AC008406.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135120526,"end":135139681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172519.9","gene_symbol":"OR10H5","gene_name":"olfactory receptor family 10 subfamily H member 5 [Source:HGNC Symbol;Acc:HGNC:15389]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284433","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15787661,"end":15801025,"strand":1,"description":"olfactory receptor family 10 subfamily H member 5 [Source:HGNC Symbol;Acc:HGNC:15389]"}, {"versioned_ensembl_gene_id":"ENSG00000069011.15","gene_symbol":"PITX1","gene_name":"paired like homeodomain 1 [Source:HGNC Symbol;Acc:HGNC:9004]","synonyms":"PTX1,POTX,BFT","biotype":"protein_coding","ncbi_id":"5307","summary":"This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family are involved in organ development and left-right asymmetry. This protein acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. [provided by RefSeq, Jul 2008]","start":135027735,"end":135034813,"strand":-1,"description":"paired like homeodomain 1 [Source:HGNC Symbol;Acc:HGNC:9004]"}, {"versioned_ensembl_gene_id":"ENSG00000180178.10","gene_symbol":"FAR2P1","gene_name":"fatty acyl-CoA reductase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49284]","synonyms":"LOC440905","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440905","summary":null,"start":129990456,"end":130051131,"strand":-1,"description":"fatty acyl-CoA reductase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49284]"}, {"versioned_ensembl_gene_id":"ENSG00000197046.11","gene_symbol":"SIGLEC15","gene_name":"sialic acid binding Ig like lectin 15 [Source:HGNC Symbol;Acc:HGNC:27596]","synonyms":"HsT1361,CD33L3","biotype":"protein_coding","ncbi_id":"284266","summary":null,"start":45825512,"end":45844080,"strand":1,"description":"sialic acid binding Ig like lectin 15 [Source:HGNC Symbol;Acc:HGNC:27596]"}, {"versioned_ensembl_gene_id":"ENSG00000259314.1","gene_symbol":"AC103739.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90604225,"end":90614558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259212.1","gene_symbol":"AC103739.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90595840,"end":90596447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186115.12","gene_symbol":"CYP4F2","gene_name":"cytochrome P450 family 4 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:2645]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8529","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. The enzyme starts the process of inactivating and degrading leukotriene B4, a potent mediator of inflammation. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F11, is approximately 16 kb away. [provided by RefSeq, Jul 2008]","start":15878023,"end":15898120,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:2645]"}, {"versioned_ensembl_gene_id":"ENSG00000249007.1","gene_symbol":"AL691482.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":202011370,"end":202015657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176393.10","gene_symbol":"RNPEP","gene_name":"arginyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:10078]","synonyms":"APB","biotype":"protein_coding","ncbi_id":"6051","summary":null,"start":201982372,"end":202006147,"strand":1,"description":"arginyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:10078]"}, {"versioned_ensembl_gene_id":"ENSG00000263267.3","gene_symbol":"AC129507.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":362640,"end":364923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270496.1","gene_symbol":"BNIP3P7","gene_name":"BCL2 interacting protein 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49101]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927265","summary":null,"start":18491904,"end":18492419,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49101]"}, {"versioned_ensembl_gene_id":"ENSG00000248337.1","gene_symbol":"AC233724.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17654373,"end":17654643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163435.15","gene_symbol":"ELF3","gene_name":"E74 like ETS transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:3318]","synonyms":"ESE-1,ERT,EPR-1,ESX","biotype":"protein_coding","ncbi_id":"1999","summary":null,"start":202007945,"end":202017188,"strand":1,"description":"E74 like ETS transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:3318]"}, {"versioned_ensembl_gene_id":"ENSG00000272981.1","gene_symbol":"AP001993.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127119326,"end":127139735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088888.17","gene_symbol":"MAVS","gene_name":"mitochondrial antiviral signaling protein [Source:HGNC Symbol;Acc:HGNC:29233]","synonyms":"VISA,KIAA1271,IPS-1,Cardif","biotype":"protein_coding","ncbi_id":"57506","summary":"This gene encodes an intermediary protein necessary in the virus-triggered beta interferon signaling pathways. It is required for activation of transcription factors which regulate expression of beta interferon and contributes to antiviral innate immunity. [provided by RefSeq, Jul 2020]","start":3846799,"end":3876123,"strand":1,"description":"mitochondrial antiviral signaling protein [Source:HGNC Symbol;Acc:HGNC:29233]"}, {"versioned_ensembl_gene_id":"ENSG00000135842.16","gene_symbol":"FAM129A","gene_name":"family with sequence similarity 129 member A [Source:HGNC Symbol;Acc:HGNC:16784]","synonyms":"NIBAN,GIG39,C1orf24","biotype":"protein_coding","ncbi_id":"116496","summary":"This gene encodes a member of the family with sequence similarity 129 protein family. This gene is highly expressed in several cancer cells and may serve as a prognostic marker for certain cancers. The encoded protein may play a role in regulating p53-mediated apoptosis. [provided by RefSeq, Sep 2016]","start":184790724,"end":184974550,"strand":-1,"description":"family with sequence similarity 129 member A [Source:HGNC Symbol;Acc:HGNC:16784]"}, {"versioned_ensembl_gene_id":"ENSG00000255988.1","gene_symbol":"TUBB4BP1","gene_name":"tubulin beta 4B class IVb pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42180]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478981","summary":null,"start":25440875,"end":25441052,"strand":-1,"description":"tubulin beta 4B class IVb pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42180]"}, {"versioned_ensembl_gene_id":"ENSG00000122733.12","gene_symbol":"PHF24","gene_name":"PHD finger protein 24 [Source:HGNC Symbol;Acc:HGNC:29180]","synonyms":"KIAA1045","biotype":"protein_coding","ncbi_id":"23349","summary":null,"start":34957608,"end":34982544,"strand":1,"description":"PHD finger protein 24 [Source:HGNC Symbol;Acc:HGNC:29180]"}, {"versioned_ensembl_gene_id":"ENSG00000223382.4","gene_symbol":"LINC01778","gene_name":"long intergenic non-protein coding RNA 1778 [Source:HGNC Symbol;Acc:HGNC:52568]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378622","summary":null,"start":30824228,"end":30834431,"strand":1,"description":"long intergenic non-protein coding RNA 1778 [Source:HGNC Symbol;Acc:HGNC:52568]"}, {"versioned_ensembl_gene_id":"ENSG00000177340.5","gene_symbol":"FLJ13224","gene_name":"uncharacterized LOC79857 [Source:NCBI gene;Acc:79857]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"79857","summary":null,"start":31324316,"end":31325829,"strand":1,"description":"uncharacterized LOC79857 [Source:NCBI gene;Acc:79857]"}, {"versioned_ensembl_gene_id":"ENSG00000231500.6","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"KE-3,S18,HKE3,KE3,D6S218E","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33272010,"end":33276510,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000231238.1","gene_symbol":"LINC00349","gene_name":"long intergenic non-protein coding RNA 349 [Source:HGNC Symbol;Acc:HGNC:42667]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874135","summary":null,"start":18540497,"end":18550697,"strand":1,"description":"long intergenic non-protein coding RNA 349 [Source:HGNC Symbol;Acc:HGNC:42667]"}, {"versioned_ensembl_gene_id":"ENSG00000108848.15","gene_symbol":"LUC7L3","gene_name":"LUC7 like 3 pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:24309]","synonyms":"CREAP-1,CRA,OA48-18,LUC7A,hLuc7A,FLJ11063,CROP","biotype":"protein_coding","ncbi_id":"51747","summary":"This gene encodes a protein with an N-terminal half that contains cysteine/histidine motifs and leucine zipper-like repeats, and the C-terminal half is rich in arginine and glutamate residues (RE domain) and arginine and serine residues (RS domain). This protein localizes with a speckled pattern in the nucleus, and could be involved in the formation of splicesome via the RE and RS domains. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2009]","start":50719544,"end":50756213,"strand":1,"description":"LUC7 like 3 pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:24309]"}, {"versioned_ensembl_gene_id":"ENSG00000233905.1","gene_symbol":"LONRF2P2","gene_name":"LON peptidase N-terminal domain and ring finger 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39829]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421799","summary":null,"start":18609132,"end":18609702,"strand":1,"description":"LON peptidase N-terminal domain and ring finger 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39829]"}, {"versioned_ensembl_gene_id":"ENSG00000260038.1","gene_symbol":"AC009090.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":57247350,"end":57248492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233680.4","gene_symbol":"HNRNPA1P27","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39545]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"664721","summary":null,"start":100887636,"end":100888590,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39545]"}, {"versioned_ensembl_gene_id":"ENSG00000234891.1","gene_symbol":"Z82196.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34703126,"end":34704885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280356.1","gene_symbol":"AL021877.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34641179,"end":34651862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284655.1","gene_symbol":"AC084121.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7680309,"end":7680526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224965.1","gene_symbol":"KCNC4-AS1","gene_name":"KCNC4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39958]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873974","summary":null,"start":110208834,"end":110209987,"strand":-1,"description":"KCNC4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39958]"}, {"versioned_ensembl_gene_id":"ENSG00000227118.3","gene_symbol":"BTF3P13","gene_name":"basic transcription factor 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:1128]","synonyms":"HUMBTFD,BTF3L3","biotype":"processed_pseudogene","ncbi_id":"132556","summary":"This locus defines a putative member of the BTF3 family of transcription factors and is thought to represent a pseudogene. [provided by RefSeq, Jul 2008]","start":98740742,"end":98741231,"strand":1,"description":"basic transcription factor 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:1128]"}, {"versioned_ensembl_gene_id":"ENSG00000249764.1","gene_symbol":"AC114811.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98713804,"end":98713971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160602.13","gene_symbol":"NEK8","gene_name":"NIMA related kinase 8 [Source:HGNC Symbol;Acc:HGNC:13387]","synonyms":"NPHP9","biotype":"protein_coding","ncbi_id":"284086","summary":"This gene encodes a member of the serine/threionine protein kinase family related to NIMA (never in mitosis, gene A) of Aspergillus nidulans. The encoded protein may play a role in cell cycle progression from G2 to M phase. Mutations in the related mouse gene are associated with a disease phenotype that closely parallels the juvenile autosomal recessive form of polycystic kidney disease in humans. [provided by RefSeq, Jul 2008]","start":28725897,"end":28743455,"strand":1,"description":"NIMA related kinase 8 [Source:HGNC Symbol;Acc:HGNC:13387]"}, {"versioned_ensembl_gene_id":"ENSG00000234248.1","gene_symbol":"AL392086.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6891457,"end":6920472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155465.18","gene_symbol":"SLC7A7","gene_name":"solute carrier family 7 member 7 [Source:HGNC Symbol;Acc:HGNC:11065]","synonyms":"y+LAT-1,LPI","biotype":"protein_coding","ncbi_id":"9056","summary":"The protein encoded by this gene is the light subunit of a cationic amino acid transporter. This sodium-independent transporter is formed when the light subunit encoded by this gene dimerizes with the heavy subunit transporter protein SLC3A2. This transporter is found in epithelial cell membranes where it transfers cationic and large neutral amino acids from the cell to the extracellular space. Defects in this gene are a cause of lysinuric protein intolerance (LPI). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2011]","start":22773222,"end":22829820,"strand":-1,"description":"solute carrier family 7 member 7 [Source:HGNC Symbol;Acc:HGNC:11065]"}, {"versioned_ensembl_gene_id":"ENSG00000265073.1","gene_symbol":"AC010761.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28732963,"end":28743102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267729.1","gene_symbol":"AC010761.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28727258,"end":28727739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223919.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31554192,"end":31556464,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000079112.9","gene_symbol":"CDH17","gene_name":"cadherin 17 [Source:HGNC Symbol;Acc:HGNC:1756]","synonyms":"HPT-1,cadherin","biotype":"protein_coding","ncbi_id":"1015","summary":"This gene is a member of the cadherin superfamily, genes encoding calcium-dependent, membrane-associated glycoproteins. The encoded protein is cadherin-like, consisting of an extracellular region, containing 7 cadherin domains, and a transmembrane region but lacking the conserved cytoplasmic domain. The protein is a component of the gastrointestinal tract and pancreatic ducts, acting as an intestinal proton-dependent peptide transporter in the first step in oral absorption of many medically important peptide-based drugs. The protein may also play a role in the morphological organization of liver and intestine. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":94127171,"end":94217303,"strand":-1,"description":"cadherin 17 [Source:HGNC Symbol;Acc:HGNC:1756]"}, {"versioned_ensembl_gene_id":"ENSG00000249780.1","gene_symbol":"AC093809.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12640298,"end":12640637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276266.1","gene_symbol":"FP325318.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40611252,"end":40622155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123454.10","gene_symbol":"DBH","gene_name":"dopamine beta-hydroxylase [Source:HGNC Symbol;Acc:HGNC:2689]","synonyms":"DBM","biotype":"protein_coding","ncbi_id":"1621","summary":"The protein encoded by this gene is an oxidoreductase belonging to the copper type II, ascorbate-dependent monooxygenase family. The encoded protein, expressed in neuroscretory vesicles and chromaffin granules of the adrenal medulla, catalyzes the conversion of dopamine to norepinephrine, which functions as both a hormone and as the main neurotransmitter of the sympathetic nervous system. The enzyme encoded by this gene exists exists in both soluble and membrane-bound forms, depending on the absence or presence, respectively, of a signal peptide. Mutations in this gene cause dopamine beta-hydroxylate deficiency in human patients, characterized by deficits in autonomic and cardiovascular function, including hypotension and ptosis. Polymorphisms in this gene may play a role in a variety of psychiatric disorders. [provided by RefSeq, Aug 2017]","start":133636360,"end":133659344,"strand":1,"description":"dopamine beta-hydroxylase [Source:HGNC Symbol;Acc:HGNC:2689]"}, {"versioned_ensembl_gene_id":"ENSG00000279116.2","gene_symbol":"OR8D2","gene_name":"olfactory receptor family 8 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8482]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"283160","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":124319238,"end":124320288,"strand":-1,"description":"olfactory receptor family 8 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8482]"}, {"versioned_ensembl_gene_id":"ENSG00000224300.1","gene_symbol":"OR51P1P","gene_name":"olfactory receptor family 51 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14762]","synonyms":"OR51P2P","biotype":"unprocessed_pseudogene","ncbi_id":"79300","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5015138,"end":5016079,"strand":1,"description":"olfactory receptor family 51 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14762]"}, {"versioned_ensembl_gene_id":"ENSG00000099864.17","gene_symbol":"PALM","gene_name":"paralemmin [Source:HGNC Symbol;Acc:HGNC:8594]","synonyms":"KIAA0270","biotype":"protein_coding","ncbi_id":"5064","summary":"This gene encodes a member of the paralemmin protein family. The product of this gene is a prenylated and palmitoylated phosphoprotein that associates with the cytoplasmic face of plasma membranes and is implicated in plasma membrane dynamics in neurons and other cell types. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]","start":708939,"end":748329,"strand":1,"description":"paralemmin [Source:HGNC Symbol;Acc:HGNC:8594]"}, {"versioned_ensembl_gene_id":"ENSG00000253824.1","gene_symbol":"AP003472.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100381260,"end":100414459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186788.13","gene_symbol":"SPATA31D3","gene_name":"SPATA31 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:38603]","synonyms":"FLJ44082,FAM75D3","biotype":"protein_coding","ncbi_id":"389762","summary":null,"start":81943586,"end":81950038,"strand":1,"description":"SPATA31 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:38603]"}, {"versioned_ensembl_gene_id":"ENSG00000274156.1","gene_symbol":"AC008121.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50934942,"end":50935464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124260.11","gene_symbol":"MAGEA10","gene_name":"MAGE family member A10 [Source:HGNC Symbol;Acc:HGNC:6797]","synonyms":"MGC10599,MAGE10,CT1.10","biotype":"protein_coding","ncbi_id":"4109","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream melanoma antigen family A, 5 (MAGEA5) gene.[provided by RefSeq, Oct 2011]","start":152133310,"end":152138578,"strand":-1,"description":"MAGE family member A10 [Source:HGNC Symbol;Acc:HGNC:6797]"}, {"versioned_ensembl_gene_id":"ENSG00000236196.8","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"NFKBIL,IKBL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31529043,"end":31540993,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000165300.7","gene_symbol":"SLITRK5","gene_name":"SLIT and NTRK like family member 5 [Source:HGNC Symbol;Acc:HGNC:20295]","synonyms":"LRRC11,KIAA0918,bA364G4.2","biotype":"protein_coding","ncbi_id":"26050","summary":"Members of the SLITRK family, such as SLITRK5, are integral membrane proteins with 2 N-terminal leucine-rich repeat (LRR) domains similar to those of SLIT proteins (see SLIT1; MIM 603742). Most SLITRKs, including SLITRK5, also have C-terminal regions that share homology with neurotrophin receptors (see NTRK1; MIM 191315). SLITRKs are expressed predominantly in neural tissues and have neurite-modulating activity (Aruga et al., 2003 [PubMed 14557068]).[supplied by OMIM, Mar 2008]","start":87672615,"end":87696272,"strand":1,"description":"SLIT and NTRK like family member 5 [Source:HGNC Symbol;Acc:HGNC:20295]"}, {"versioned_ensembl_gene_id":"ENSG00000261196.1","gene_symbol":"CYP4A43P","gene_name":"cytochrome P450 family 4 subfamily A member 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:42417]","synonyms":"CYP4A-se2[1]","biotype":"unprocessed_pseudogene","ncbi_id":"100874495","summary":null,"start":46994382,"end":46994502,"strand":-1,"description":"cytochrome P450 family 4 subfamily A member 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:42417]"}, {"versioned_ensembl_gene_id":"ENSG00000278122.1","gene_symbol":"AQP7P5","gene_name":"aquaporin 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51836]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102724655","summary":null,"start":40481558,"end":40497592,"strand":-1,"description":"aquaporin 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51836]"}, {"versioned_ensembl_gene_id":"ENSG00000165863.16","gene_symbol":"C10orf82","gene_name":"chromosome 10 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:28500]","synonyms":"MGC33547,Em:AC016825.4","biotype":"protein_coding","ncbi_id":"143379","summary":null,"start":116663696,"end":116670264,"strand":-1,"description":"chromosome 10 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:28500]"}, {"versioned_ensembl_gene_id":"ENSG00000103512.14","gene_symbol":"NOMO1","gene_name":"NODAL modulator 1 [Source:HGNC Symbol;Acc:HGNC:30060]","synonyms":"PM5","biotype":"protein_coding","ncbi_id":"23420","summary":"This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a region of duplication located on the p arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum (PXE). [provided by RefSeq, Jul 2008]","start":14833681,"end":14896160,"strand":1,"description":"NODAL modulator 1 [Source:HGNC Symbol;Acc:HGNC:30060]"}, {"versioned_ensembl_gene_id":"ENSG00000272950.1","gene_symbol":"AC093799.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98322853,"end":98323430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125347.13","gene_symbol":"IRF1","gene_name":"interferon regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:6116]","synonyms":"MAR","biotype":"protein_coding","ncbi_id":"3659","summary":"The protein encoded by this gene is a transcriptional regulator and tumor suppressor, serving as an activator of genes involved in both innate and acquired immune responses. The encoded protein activates the transcription of genes involved in the body's response to viruses and bacteria, playing a role in cell proliferation, apoptosis, the immune response, and DNA damage response. This protein represses the transcription of several other genes. As a tumor suppressor, it both suppresses tumor cell growth and stimulates an immune response against tumor cells. Defects in this gene have been associated with gastric cancer, myelogenous leukemia, and lung cancer. [provided by RefSeq, Aug 2017]","start":132481609,"end":132490798,"strand":-1,"description":"interferon regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:6116]"}, {"versioned_ensembl_gene_id":"ENSG00000186074.18","gene_symbol":"CD300LF","gene_name":"CD300 molecule like family member f [Source:HGNC Symbol;Acc:HGNC:29883]","synonyms":"CD300f,NKIR,IREM1,IGSF13,CLM1","biotype":"protein_coding","ncbi_id":"146722","summary":"This gene encodes a member of the CD300 protein family. Members of this family are cell surface glycoproteins with a single IgV-like extracellular domain, and are involved in the regulation of immune response. The encoded protein is an inhibitory receptor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":74694311,"end":74712978,"strand":-1,"description":"CD300 molecule like family member f [Source:HGNC Symbol;Acc:HGNC:29883]"}, {"versioned_ensembl_gene_id":"ENSG00000101160.13","gene_symbol":"CTSZ","gene_name":"cathepsin Z [Source:HGNC Symbol;Acc:HGNC:2547]","synonyms":"CTSX","biotype":"protein_coding","ncbi_id":"1522","summary":"The protein encoded by this gene is a lysosomal cysteine proteinase and member of the peptidase C1 family. It exhibits both carboxy-monopeptidase and carboxy-dipeptidase activities. The encoded protein has also been known as cathepsin X and cathepsin P. This gene is expressed ubiquitously in cancer cell lines and primary tumors and, like other members of this family, may be involved in tumorigenesis. [provided by RefSeq, Oct 2008]","start":58995185,"end":59007247,"strand":-1,"description":"cathepsin Z [Source:HGNC Symbol;Acc:HGNC:2547]"}, {"versioned_ensembl_gene_id":"ENSG00000174695.9","gene_symbol":"TMEM167A","gene_name":"transmembrane protein 167A [Source:HGNC Symbol;Acc:HGNC:28330]","synonyms":"TMEM167,MGC23909,FLJ30508","biotype":"protein_coding","ncbi_id":"153339","summary":null,"start":83052846,"end":83077863,"strand":-1,"description":"transmembrane protein 167A [Source:HGNC Symbol;Acc:HGNC:28330]"}, {"versioned_ensembl_gene_id":"ENSG00000168348.3","gene_symbol":"INSM2","gene_name":"INSM transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:17539]","synonyms":"Mlt1,IA-6","biotype":"protein_coding","ncbi_id":"84684","summary":null,"start":35534042,"end":35537054,"strand":1,"description":"INSM transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:17539]"}, {"versioned_ensembl_gene_id":"ENSG00000253580.1","gene_symbol":"TRMT10BP1","gene_name":"tRNA methyltransferase 10B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52409]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108652373,"end":108653315,"strand":1,"description":"tRNA methyltransferase 10B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52409]"}, {"versioned_ensembl_gene_id":"ENSG00000280425.2","gene_symbol":"AL357673.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54137746,"end":54142980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259105.1","gene_symbol":"RPS3AP4","gene_name":"ribosomal protein S3A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132142","summary":null,"start":35468272,"end":35469330,"strand":1,"description":"ribosomal protein S3A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23562]"}, {"versioned_ensembl_gene_id":"ENSG00000257790.1","gene_symbol":"EIF4A1P4","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728698","summary":null,"start":53153272,"end":53154484,"strand":1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37923]"}, {"versioned_ensembl_gene_id":"ENSG00000186452.10","gene_symbol":"TMPRSS12","gene_name":"transmembrane protease, serine 12 [Source:HGNC Symbol;Acc:HGNC:28779]","synonyms":"MGC57341,CT151","biotype":"protein_coding","ncbi_id":"283471","summary":null,"start":50842920,"end":50887884,"strand":1,"description":"transmembrane protease, serine 12 [Source:HGNC Symbol;Acc:HGNC:28779]"}, {"versioned_ensembl_gene_id":"ENSG00000128602.9","gene_symbol":"SMO","gene_name":"smoothened, frizzled class receptor [Source:HGNC Symbol;Acc:HGNC:11119]","synonyms":"SMOH,FZD11","biotype":"protein_coding","ncbi_id":"6608","summary":"The protein encoded by this gene is a G protein-coupled receptor that interacts with the patched protein, a receptor for hedgehog proteins. The encoded protein tranduces signals to other proteins after activation by a hedgehog protein/patched protein complex. [provided by RefSeq, Jul 2010]","start":129188872,"end":129213545,"strand":1,"description":"smoothened, frizzled class receptor [Source:HGNC Symbol;Acc:HGNC:11119]"}, {"versioned_ensembl_gene_id":"ENSG00000121274.12","gene_symbol":"PAPD5","gene_name":"poly(A) RNA polymerase D5, non-canonical [Source:HGNC Symbol;Acc:HGNC:30758]","synonyms":"TRF4-2","biotype":"protein_coding","ncbi_id":"64282","summary":null,"start":50152918,"end":50235310,"strand":1,"description":"poly(A) RNA polymerase D5, non-canonical [Source:HGNC Symbol;Acc:HGNC:30758]"}, {"versioned_ensembl_gene_id":"ENSG00000240542.4","gene_symbol":"KRTAP9-1","gene_name":"keratin associated protein 9-1 [Source:HGNC Symbol;Acc:HGNC:18912]","synonyms":"KRTAP9L3,KAP9.1","biotype":"protein_coding","ncbi_id":"728318","summary":null,"start":41189887,"end":41190639,"strand":1,"description":"keratin associated protein 9-1 [Source:HGNC Symbol;Acc:HGNC:18912]"}, {"versioned_ensembl_gene_id":"ENSG00000178105.9","gene_symbol":"DDX10","gene_name":"DEAD-box helicase 10 [Source:HGNC Symbol;Acc:HGNC:2735]","synonyms":"HRH-J8,Dbp4","biotype":"protein_coding","ncbi_id":"1662","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, and it may be involved in ribosome assembly. Fusion of this gene and the nucleoporin gene, NUP98, by inversion 11 (p15q22) chromosome translocation is found in the patients with de novo or therapy-related myeloid malignancies. [provided by RefSeq, Jul 2008]","start":108665025,"end":108940930,"strand":1,"description":"DEAD-box helicase 10 [Source:HGNC Symbol;Acc:HGNC:2735]"}, {"versioned_ensembl_gene_id":"ENSG00000231390.1","gene_symbol":"SNX18P8","gene_name":"sorting nexin 18 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39616]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418981","summary":null,"start":40293082,"end":40293955,"strand":1,"description":"sorting nexin 18 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39616]"}, {"versioned_ensembl_gene_id":"ENSG00000267898.1","gene_symbol":"AC026803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48963975,"end":48965158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248487.8","gene_symbol":"ABHD14A","gene_name":"abhydrolase domain containing 14A [Source:HGNC Symbol;Acc:HGNC:24538]","synonyms":"DORZ1,DKFZP564O243","biotype":"protein_coding","ncbi_id":"25864","summary":null,"start":51971426,"end":51981199,"strand":1,"description":"abhydrolase domain containing 14A [Source:HGNC Symbol;Acc:HGNC:24538]"}, {"versioned_ensembl_gene_id":"ENSG00000204345.1","gene_symbol":"CD300LD","gene_name":"CD300 molecule like family member d [Source:HGNC Symbol;Acc:HGNC:16848]","synonyms":"CMRF35A4,CD300D","biotype":"protein_coding","ncbi_id":"100131439","summary":null,"start":74579365,"end":74592283,"strand":-1,"description":"CD300 molecule like family member d [Source:HGNC Symbol;Acc:HGNC:16848]"}, {"versioned_ensembl_gene_id":"ENSG00000221880.3","gene_symbol":"KRTAP1-3","gene_name":"keratin associated protein 1-3 [Source:HGNC Symbol;Acc:HGNC:16771]","synonyms":"KAP1.3","biotype":"protein_coding","ncbi_id":"81850","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41033884,"end":41034855,"strand":-1,"description":"keratin associated protein 1-3 [Source:HGNC Symbol;Acc:HGNC:16771]"}, {"versioned_ensembl_gene_id":"ENSG00000212901.3","gene_symbol":"KRTAP3-1","gene_name":"keratin associated protein 3-1 [Source:HGNC Symbol;Acc:HGNC:16778]","synonyms":"KAP3.1","biotype":"protein_coding","ncbi_id":"83896","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41008521,"end":41019324,"strand":-1,"description":"keratin associated protein 3-1 [Source:HGNC Symbol;Acc:HGNC:16778]"}, {"versioned_ensembl_gene_id":"ENSG00000206282.11","gene_symbol":"RGL2","gene_name":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]","synonyms":"KE1.5,HKE1.5,RAB2L","biotype":"protein_coding","ncbi_id":"5863","summary":null,"start":33220485,"end":33228152,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]"}, {"versioned_ensembl_gene_id":"ENSG00000274245.1","gene_symbol":"AL391597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207372559,"end":207373252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008513.14","gene_symbol":"ST3GAL1","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10862]","synonyms":"ST3O,ST3GalA.1,SIATFL,SIAT4A","biotype":"protein_coding","ncbi_id":"6482","summary":"The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi but can be proteolytically processed to a soluble form. Correct glycosylation of the encoded protein may be critical to its sialyltransferase activity. This protein, which is a member of glycosyltransferase family 29, can use the same acceptor substrates as does sialyltransferase 4B. Two transcript variants encoding the same protein have been found for this gene. Other transcript variants may exist, but have not been fully characterized yet. [provided by RefSeq, Jul 2008]","start":133454848,"end":133571940,"strand":-1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10862]"}, {"versioned_ensembl_gene_id":"ENSG00000250273.1","gene_symbol":"PSMC1P5","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480732","summary":null,"start":107195156,"end":107195332,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39780]"}, {"versioned_ensembl_gene_id":"ENSG00000174485.15","gene_symbol":"DENND4A","gene_name":"DENN domain containing 4A [Source:HGNC Symbol;Acc:HGNC:24321]","synonyms":"MYCPBP,IRLB","biotype":"protein_coding","ncbi_id":"10260","summary":"This gene encodes a DENN domain-containing protein that may function as a guanine nucleotide exchange factor that specifically activates ras-related protein Rab-10. This protein also contains a interferon stimulated response element-binding domain and may be involved in regulating the v-myc avian myelocytomatosis viral (MYC) oncogene. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 8. [provided by RefSeq, Mar 2016]","start":65658046,"end":65792293,"strand":-1,"description":"DENN domain containing 4A [Source:HGNC Symbol;Acc:HGNC:24321]"}, {"versioned_ensembl_gene_id":"ENSG00000283083.1","gene_symbol":"LINC02498","gene_name":"long intergenic non-protein coding RNA 2498 [Source:HGNC Symbol;Acc:HGNC:53483]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723525","summary":null,"start":10737572,"end":10749586,"strand":1,"description":"long intergenic non-protein coding RNA 2498 [Source:HGNC Symbol;Acc:HGNC:53483]"}, {"versioned_ensembl_gene_id":"ENSG00000249334.1","gene_symbol":"AC084048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10685003,"end":10697661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254467.1","gene_symbol":"AP002765.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123668499,"end":123671637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178235.7","gene_symbol":"SLITRK1","gene_name":"SLIT and NTRK like family member 1 [Source:HGNC Symbol;Acc:HGNC:20297]","synonyms":"LRRC12,KIAA1910","biotype":"protein_coding","ncbi_id":"114798","summary":"This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. However, the protein encoded by this gene lacks the region of homology to neurotrophin receptors. This protein is thought to be involved in neurite outgrowth. Mutations in this gene may be associated with Tourette syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":83877205,"end":83882393,"strand":-1,"description":"SLIT and NTRK like family member 1 [Source:HGNC Symbol;Acc:HGNC:20297]"}, {"versioned_ensembl_gene_id":"ENSG00000224617.1","gene_symbol":"BX276092.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71789386,"end":71789636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255745.1","gene_symbol":"AC023796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24704565,"end":24774213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247311.2","gene_symbol":"AC010255.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122128762,"end":122154856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243537.1","gene_symbol":"KC877373.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133325997,"end":133326404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279270.2","gene_symbol":"OR52R1","gene_name":"olfactory receptor family 52 subfamily R member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15235]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"119695","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":4803433,"end":4804380,"strand":-1,"description":"olfactory receptor family 52 subfamily R member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15235]"}, {"versioned_ensembl_gene_id":"ENSG00000176895.9","gene_symbol":"OR51A7","gene_name":"olfactory receptor family 51 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:15188]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119687","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4903783,"end":4909462,"strand":1,"description":"olfactory receptor family 51 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:15188]"}, {"versioned_ensembl_gene_id":"ENSG00000272634.2","gene_symbol":"AC103710.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4709569,"end":4712421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095110.7","gene_symbol":"NXPE1","gene_name":"neurexophilin and PC-esterase domain family member 1 [Source:HGNC Symbol;Acc:HGNC:28527]","synonyms":"MGC34290,FAM55A","biotype":"protein_coding","ncbi_id":"120400","summary":null,"start":114521715,"end":114559895,"strand":-1,"description":"neurexophilin and PC-esterase domain family member 1 [Source:HGNC Symbol;Acc:HGNC:28527]"}, {"versioned_ensembl_gene_id":"ENSG00000186599.7","gene_symbol":"DEFB105B","gene_name":"defensin beta 105B [Source:HGNC Symbol;Acc:HGNC:29930]","synonyms":null,"biotype":"protein_coding","ncbi_id":"504180","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 105, DEFB105A and DEFB105B, in tail-to-tail orientation. This gene, DEFB105B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7487669,"end":7489593,"strand":1,"description":"defensin beta 105B [Source:HGNC Symbol;Acc:HGNC:29930]"}, {"versioned_ensembl_gene_id":"ENSG00000226627.1","gene_symbol":"SHANK2-AS1","gene_name":"SHANK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40014]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874198","summary":null,"start":70631094,"end":70635490,"strand":1,"description":"SHANK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40014]"}, {"versioned_ensembl_gene_id":"ENSG00000143376.12","gene_symbol":"SNX27","gene_name":"sorting nexin family member 27 [Source:HGNC Symbol;Acc:HGNC:20073]","synonyms":"MY014,MGC20471,KIAA0488","biotype":"protein_coding","ncbi_id":"81609","summary":"This gene encodes a member of the sorting nexin family, a diverse group of cytoplasmic and membrane-associated proteins involved in endocytosis of plasma membrane receptors and protein trafficking through these compartments. All members of this protein family contain a phosphoinositide binding domain (PX domain). A highly similar protein in mouse is responsible for the specific recruitment of an isoform of serotonin 5-hydroxytryptamine 4 receptor into early endosomes, suggesting the analogous role for the human protein. [provided by RefSeq, Jul 2008]","start":151612065,"end":151699091,"strand":1,"description":"sorting nexin family member 27 [Source:HGNC Symbol;Acc:HGNC:20073]"}, {"versioned_ensembl_gene_id":"ENSG00000224443.1","gene_symbol":"AC006509.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47705468,"end":47705979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225818.1","gene_symbol":"AC118653.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71596338,"end":71597279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273287.2","gene_symbol":"AL008718.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45262273,"end":45263585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226241.2","gene_symbol":"Z75746.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103087198,"end":103089277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265458.1","gene_symbol":"AC132938.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82454273,"end":82458521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267507.1","gene_symbol":"AC010327.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55119250,"end":55120383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227517.6","gene_symbol":"LINC01483","gene_name":"long intergenic non-protein coding RNA 1483 [Source:HGNC Symbol;Acc:HGNC:51130]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928122","summary":null,"start":69577251,"end":69903000,"strand":1,"description":"long intergenic non-protein coding RNA 1483 [Source:HGNC Symbol;Acc:HGNC:51130]"}, {"versioned_ensembl_gene_id":"ENSG00000101158.13","gene_symbol":"NELFCD","gene_name":"negative elongation factor complex member C/D [Source:HGNC Symbol;Acc:HGNC:15934]","synonyms":"TH1L,TH1,NELF-D,NELF-C,HSPC130","biotype":"protein_coding","ncbi_id":"51497","summary":"The NELF complex of proteins interacts with the DSIF protein complex to repress transcriptional elongation by RNA polymerase II. The protein encoded by this gene is an essential part of the NELF complex. Alternative translation initiation site usage results in the formation of two isoforms with different N-termini. [provided by RefSeq, Jul 2008]","start":58981208,"end":58995133,"strand":1,"description":"negative elongation factor complex member C/D [Source:HGNC Symbol;Acc:HGNC:15934]"}, {"versioned_ensembl_gene_id":"ENSG00000170374.5","gene_symbol":"SP7","gene_name":"Sp7 transcription factor [Source:HGNC Symbol;Acc:HGNC:17321]","synonyms":"OSX,osterix","biotype":"protein_coding","ncbi_id":"121340","summary":"This gene encodes a member of the Sp subfamily of Sp/XKLF transcription factors. Sp family proteins are sequence-specific DNA-binding proteins characterized by an amino-terminal trans-activation domain and three carboxy-terminal zinc finger motifs. This protein is a bone specific transcription factor and is required for osteoblast differentiation and bone formation.[provided by RefSeq, Jul 2010]","start":53326575,"end":53345315,"strand":-1,"description":"Sp7 transcription factor [Source:HGNC Symbol;Acc:HGNC:17321]"}, {"versioned_ensembl_gene_id":"ENSG00000231427.5","gene_symbol":"LINC01445","gene_name":"long intergenic non-protein coding RNA 1445 [Source:HGNC Symbol;Acc:HGNC:50771]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723605","summary":null,"start":54330697,"end":54349849,"strand":1,"description":"long intergenic non-protein coding RNA 1445 [Source:HGNC Symbol;Acc:HGNC:50771]"}, {"versioned_ensembl_gene_id":"ENSG00000280920.1","gene_symbol":"HPVC1","gene_name":"human papillomavirus (type 18) E5 central sequence-like 1 [Source:HGNC Symbol;Acc:HGNC:5169]","synonyms":"PE5L,HPV18E5L","biotype":"lincRNA","ncbi_id":"3262","summary":null,"start":54201224,"end":54202421,"strand":1,"description":"human papillomavirus (type 18) E5 central sequence-like 1 [Source:HGNC Symbol;Acc:HGNC:5169]"}, {"versioned_ensembl_gene_id":"ENSG00000258658.1","gene_symbol":"AL139021.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58370023,"end":58395641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238131.1","gene_symbol":"AC073521.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53926676,"end":53947744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235454.1","gene_symbol":"HAUS6P3","gene_name":"HAUS augmin like complex subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723574","summary":null,"start":53862233,"end":53863339,"strand":1,"description":"HAUS augmin like complex subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50772]"}, {"versioned_ensembl_gene_id":"ENSG00000226683.2","gene_symbol":"PWWP2AP1","gene_name":"PWWP domain containing 2A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39709]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129459","summary":null,"start":80654755,"end":80657027,"strand":1,"description":"PWWP domain containing 2A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39709]"}, {"versioned_ensembl_gene_id":"ENSG00000270450.1","gene_symbol":"IGKV2OR2-7","gene_name":"immunoglobulin kappa variable 2/OR2-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5810]","synonyms":"IGKV2/OR2-7","biotype":"IG_V_pseudogene","ncbi_id":"652873","summary":null,"start":97372532,"end":97372835,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5810]"}, {"versioned_ensembl_gene_id":"ENSG00000254213.2","gene_symbol":"FAM213AP2","gene_name":"family with sequence similarity 213 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52408]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131252","summary":null,"start":73277364,"end":73278046,"strand":-1,"description":"family with sequence similarity 213 member A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52408]"}, {"versioned_ensembl_gene_id":"ENSG00000228154.3","gene_symbol":"AC092436.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25622777,"end":25623601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163319.10","gene_symbol":"MRPS18C","gene_name":"mitochondrial ribosomal protein S18C [Source:HGNC Symbol;Acc:HGNC:16633]","synonyms":"MRPS18-1,FLJ22967,FLJ11146,CGI-134","biotype":"protein_coding","ncbi_id":"51023","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 8p, 12p, 15q, and 22q. [provided by RefSeq, Jul 2008]","start":83455932,"end":83469735,"strand":1,"description":"mitochondrial ribosomal protein S18C [Source:HGNC Symbol;Acc:HGNC:16633]"}, {"versioned_ensembl_gene_id":"ENSG00000248608.2","gene_symbol":"AC133963.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25504997,"end":25506675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283462.1","gene_symbol":"AC008505.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":103880129,"end":103891393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260160.1","gene_symbol":"AC011468.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":52058490,"end":52063703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258576.1","gene_symbol":"AL163974.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":100587775,"end":100589326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138709.17","gene_symbol":"LARP1B","gene_name":"La ribonucleoprotein domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24704]","synonyms":"LARP2,FLJ10378,DKFZp686E0316,DKFZp434K245","biotype":"protein_coding","ncbi_id":"55132","summary":"This gene encodes a protein containing domains found in the La related protein of Drosophila melanogaster. La motif-containing proteins are thought to be RNA-binding proteins, where the La motif and adjacent amino acids fold into an RNA recognition motif. The La motif is also found in proteins unrelated to the La protein. Alternative splicing has been observed at this locus and multiple variants, encoding distinct isoforms, are described. Additional splice variation has been identified but the full-length nature of these transcripts has not been determined. [provided by RefSeq, Jun 2013]","start":128061268,"end":128222931,"strand":1,"description":"La ribonucleoprotein domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24704]"}, {"versioned_ensembl_gene_id":"ENSG00000167600.13","gene_symbol":"CYP2S1","gene_name":"cytochrome P450 family 2 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15654]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29785","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. In rodents, the homologous protein has been shown to metabolize certain carcinogens; however, the specific function of the human protein has not been determined. [provided by RefSeq, Jul 2008]","start":41193049,"end":41207539,"strand":1,"description":"cytochrome P450 family 2 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:15654]"}, {"versioned_ensembl_gene_id":"ENSG00000260538.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29800445,"end":29802452,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000264808.1","gene_symbol":"AC068025.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29369717,"end":29390777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259477.1","gene_symbol":"AC012653.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57979716,"end":57980646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154262.12","gene_symbol":"ABCA6","gene_name":"ATP binding cassette subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:36]","synonyms":"EST155051","biotype":"protein_coding","ncbi_id":"23460","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24 and may play a role in macrophage lipid homeostasis. [provided by RefSeq, Jul 2008]","start":69078702,"end":69141888,"strand":-1,"description":"ATP binding cassette subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:36]"}, {"versioned_ensembl_gene_id":"ENSG00000276561.4","gene_symbol":"IRF7","gene_name":"interferon regulatory factor 7 [Source:HGNC Symbol;Acc:HGNC:6122]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3665","summary":"IRF7 encodes interferon regulatory factor 7, a member of the interferon regulatory transcription factor (IRF) family. IRF7 has been shown to play a role in the transcriptional activation of virus-inducible cellular genes, including interferon beta chain genes. Inducible expression of IRF7 is largely restricted to lymphoid tissue. Multiple IRF7 transcript variants have been identified, although the functional consequences of these have not yet been established. [provided by RefSeq, Jul 2008]","start":612805,"end":616257,"strand":-1,"description":"interferon regulatory factor 7 [Source:HGNC Symbol;Acc:HGNC:6122]"}, {"versioned_ensembl_gene_id":"ENSG00000234477.1","gene_symbol":"AC004231.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40921430,"end":40975926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237837.1","gene_symbol":"AC159540.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97301729,"end":97304151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250922.1","gene_symbol":"ATP5EP1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:839]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"23744","summary":null,"start":105532475,"end":105532630,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:839]"}, {"versioned_ensembl_gene_id":"ENSG00000196961.12","gene_symbol":"AP2A1","gene_name":"adaptor related protein complex 2 alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:561]","synonyms":"CLAPA1,ADTAA","biotype":"protein_coding","ncbi_id":"160","summary":"This gene encodes the alpha 1 adaptin subunit of the adaptor protein 2 (AP-2) complex found in clathrin coated vesicles. The AP-2 complex is a heterotetramer consisting of two large adaptins (alpha or beta), a medium adaptin (mu), and a small adaptin (sigma). The complex is part of the protein coat on the cytoplasmic face of coated vesicles which links clathrin to receptors in vesicles. Alternative splicing of this gene results in two transcript variants encoding two different isoforms. A third transcript variant has been described, but its full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":49766968,"end":49807113,"strand":1,"description":"adaptor related protein complex 2 alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:561]"}, {"versioned_ensembl_gene_id":"ENSG00000235149.1","gene_symbol":"AC096659.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":185918140,"end":185919460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164715.5","gene_symbol":"LMTK2","gene_name":"lemur tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:17880]","synonyms":"PPP1R100,LMR2,KPI2,KPI-2,KIAA1079,cprk,BREK,AATYK2","biotype":"protein_coding","ncbi_id":"22853","summary":"The protein encoded by this gene belongs to the protein kinase superfamily and the protein tyrosine kinase family. It contains N-terminal transmembrane helices and a long C-terminal cytoplasmic tail with serine/threonine/tyrosine kinase activity. This protein interacts with several other proteins, such as Inhibitor-2 (Inh2), protein phosphatase-1 (PP1C), p35, and myosin VI. It phosporylates other proteins, and is itself also phosporylated when interacting with cyclin-dependent kinase 5 (cdk5)/p35 complex. This protein involves in nerve growth factor (NGF)-TrkA signalling, and also plays a critical role in endosomal membrane trafficking. Mouse studies suggested an essential role of this protein in spermatogenesis. [provided by RefSeq, Oct 2009]","start":98106885,"end":98209633,"strand":1,"description":"lemur tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:17880]"}, {"versioned_ensembl_gene_id":"ENSG00000136888.6","gene_symbol":"ATP6V1G1","gene_name":"ATPase H+ transporting V1 subunit G1 [Source:HGNC Symbol;Acc:HGNC:864]","synonyms":"ATP6J,ATP6GL,ATP6G1,ATP6G,Vma10,DKFZp547P234","biotype":"protein_coding","ncbi_id":"9550","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. The protein encoded by this gene is one of three V1 domain G subunit proteins. Pseudogenes of this gene have been characterized. [provided by RefSeq, Jul 2008]","start":114587746,"end":114598373,"strand":1,"description":"ATPase H+ transporting V1 subunit G1 [Source:HGNC Symbol;Acc:HGNC:864]"}, {"versioned_ensembl_gene_id":"ENSG00000223977.1","gene_symbol":"AC138623.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83218890,"end":83219105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226108.2","gene_symbol":"RAB28P1","gene_name":"RAB28, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133203","summary":null,"start":39734670,"end":39735628,"strand":1,"description":"RAB28, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50380]"}, {"versioned_ensembl_gene_id":"ENSG00000139697.13","gene_symbol":"SBNO1","gene_name":"strawberry notch homolog 1 [Source:HGNC Symbol;Acc:HGNC:22973]","synonyms":"Sno,MOP3,FLJ10833,FLJ10701","biotype":"protein_coding","ncbi_id":"55206","summary":null,"start":123289109,"end":123364843,"strand":-1,"description":"strawberry notch homolog 1 [Source:HGNC Symbol;Acc:HGNC:22973]"}, {"versioned_ensembl_gene_id":"ENSG00000206478.5","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30732716,"end":30734071,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000138834.12","gene_symbol":"MAPK8IP3","gene_name":"mitogen-activated protein kinase 8 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:6884]","synonyms":"syd,KIAA1066,JSAP1,JIP3","biotype":"protein_coding","ncbi_id":"23162","summary":"The protein encoded by this gene shares similarity with the product of Drosophila syd gene, required for the functional interaction of kinesin I with axonal cargo. Studies of the similar gene in mouse suggested that this protein may interact with, and regulate the activity of numerous protein kinases of the JNK signaling pathway, and thus function as a scaffold protein in neuronal cells. The C. elegans counterpart of this gene is found to regulate synaptic vesicle transport possibly by integrating JNK signaling and kinesin-1 transport. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":1706183,"end":1770317,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:6884]"}, {"versioned_ensembl_gene_id":"ENSG00000187049.9","gene_symbol":"TMEM216","gene_name":"transmembrane protein 216 [Source:HGNC Symbol;Acc:HGNC:25018]","synonyms":"MKS2,MGC13379,JBTS2,HSPC244,CORS2","biotype":"protein_coding","ncbi_id":"51259","summary":"This locus encodes a transmembrane domain-containing protein. Mutations at this locus have been associated with Meckel-Gruber Syndrome Type 2, and Joubert Syndrome 2, also known as Cerebello-oculorenal Syndrome 2. [provided by RefSeq, Aug 2010]","start":61391687,"end":61398863,"strand":1,"description":"transmembrane protein 216 [Source:HGNC Symbol;Acc:HGNC:25018]"}, {"versioned_ensembl_gene_id":"ENSG00000229560.1","gene_symbol":"LYARP1","gene_name":"Ly1 antibody reactive pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50747]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420968","summary":null,"start":82268427,"end":82269927,"strand":-1,"description":"Ly1 antibody reactive pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50747]"}, {"versioned_ensembl_gene_id":"ENSG00000253636.1","gene_symbol":"AC022893.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73052178,"end":73063061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255753.1","gene_symbol":"AC009533.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9314402,"end":9316173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236054.1","gene_symbol":"Z82246.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32583300,"end":32584204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172366.19","gene_symbol":"MCRIP2","gene_name":"MAPK regulated corepressor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:14142]","synonyms":"MGC15416,FAM195A,C16orf14","biotype":"protein_coding","ncbi_id":"84331","summary":null,"start":636817,"end":648474,"strand":1,"description":"MAPK regulated corepressor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:14142]"}, {"versioned_ensembl_gene_id":"ENSG00000228201.1","gene_symbol":"AL022341.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":648473,"end":649200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141551.14","gene_symbol":"CSNK1D","gene_name":"casein kinase 1 delta [Source:HGNC Symbol;Acc:HGNC:2452]","synonyms":"HCKID,CKIdelta,CKID","biotype":"protein_coding","ncbi_id":"1453","summary":"This gene is a member of the casein kinase I (CKI) gene family whose members have been implicated in the control of cytoplasmic and nuclear processes, including DNA replication and repair. The encoded protein may also be involved in the regulation of apoptosis, circadian rhythm, microtubule dynamics, chromosome segregation, and p53-mediated effects on growth. The encoded protein is highly similar to the mouse and rat CK1 delta homologs. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]","start":82239023,"end":82273731,"strand":-1,"description":"casein kinase 1 delta [Source:HGNC Symbol;Acc:HGNC:2452]"}, {"versioned_ensembl_gene_id":"ENSG00000248895.1","gene_symbol":"AC068531.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48881122,"end":48881316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232926.1","gene_symbol":"AC000078.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19887289,"end":19887970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123689.5","gene_symbol":"G0S2","gene_name":"G0/G1 switch 2 [Source:HGNC Symbol;Acc:HGNC:30229]","synonyms":null,"biotype":"protein_coding","ncbi_id":"50486","summary":null,"start":209675420,"end":209676388,"strand":1,"description":"G0/G1 switch 2 [Source:HGNC Symbol;Acc:HGNC:30229]"}, {"versioned_ensembl_gene_id":"ENSG00000279495.1","gene_symbol":"AL928654.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":105370418,"end":105372918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277807.5","gene_symbol":"LILRB1","gene_name":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]","synonyms":"LIR1,PIRB,CD85,LIR-1,PIR-B,ILT2,MIR-7,CD85j","biotype":"protein_coding","ncbi_id":"10859","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54547681,"end":54568080,"strand":1,"description":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]"}, {"versioned_ensembl_gene_id":"ENSG00000113273.15","gene_symbol":"ARSB","gene_name":"arylsulfatase B [Source:HGNC Symbol;Acc:HGNC:714]","synonyms":null,"biotype":"protein_coding","ncbi_id":"411","summary":"Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2016]","start":78777209,"end":78986087,"strand":-1,"description":"arylsulfatase B [Source:HGNC Symbol;Acc:HGNC:714]"}, {"versioned_ensembl_gene_id":"ENSG00000106336.12","gene_symbol":"FBXO24","gene_name":"F-box protein 24 [Source:HGNC Symbol;Acc:HGNC:13595]","synonyms":"FBX24","biotype":"protein_coding","ncbi_id":"26261","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009]","start":100583982,"end":100601117,"strand":1,"description":"F-box protein 24 [Source:HGNC Symbol;Acc:HGNC:13595]"}, {"versioned_ensembl_gene_id":"ENSG00000268970.1","gene_symbol":"AC022150.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52597699,"end":52598887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123870.10","gene_symbol":"ZNF137P","gene_name":"zinc finger protein 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:12921]","synonyms":"ZNF137,pHZ-30","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"7696","summary":null,"start":52588505,"end":52597345,"strand":1,"description":"zinc finger protein 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:12921]"}, {"versioned_ensembl_gene_id":"ENSG00000183826.16","gene_symbol":"BTBD9","gene_name":"BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:21228]","synonyms":"KIAA1880,dJ322I12.1","biotype":"protein_coding","ncbi_id":"114781","summary":"This locus encodes a BTB/POZ domain-containing protein. This domain is known to be involved in protein-protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011]","start":38168451,"end":38640148,"strand":-1,"description":"BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:21228]"}, {"versioned_ensembl_gene_id":"ENSG00000224340.1","gene_symbol":"AL590639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10054445,"end":10054781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143353.11","gene_symbol":"LYPLAL1","gene_name":"lysophospholipase like 1 [Source:HGNC Symbol;Acc:HGNC:20440]","synonyms":"Q96AV0","biotype":"protein_coding","ncbi_id":"127018","summary":null,"start":219173844,"end":219212865,"strand":1,"description":"lysophospholipase like 1 [Source:HGNC Symbol;Acc:HGNC:20440]"}, {"versioned_ensembl_gene_id":"ENSG00000234881.1","gene_symbol":"PIGFP2","gene_name":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422349","summary":null,"start":123843036,"end":123843686,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45150]"}, {"versioned_ensembl_gene_id":"ENSG00000253542.7","gene_symbol":"SDR16C6P","gene_name":"short chain dehydrogenase/reductase family 16C member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:35413]","synonyms":"SDR16C6","biotype":"transcribed_unitary_pseudogene","ncbi_id":"442388","summary":null,"start":56373064,"end":56395365,"strand":-1,"description":"short chain dehydrogenase/reductase family 16C member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:35413]"}, {"versioned_ensembl_gene_id":"ENSG00000217612.2","gene_symbol":"AL031119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145489630,"end":145492092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270638.1","gene_symbol":"AL023806.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145735570,"end":145737218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230872.1","gene_symbol":"MFSD13B","gene_name":"major facilitator superfamily domain containing 13B [Source:HGNC Symbol;Acc:HGNC:52163]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"105371130","summary":null,"start":22382436,"end":22407428,"strand":1,"description":"major facilitator superfamily domain containing 13B [Source:HGNC Symbol;Acc:HGNC:52163]"}, {"versioned_ensembl_gene_id":"ENSG00000249851.1","gene_symbol":"RPS27AP18","gene_name":"ribosomal protein S27a pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52299]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419548","summary":null,"start":138266996,"end":138267757,"strand":-1,"description":"ribosomal protein S27a pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52299]"}, {"versioned_ensembl_gene_id":"ENSG00000108654.13","gene_symbol":"DDX5","gene_name":"DEAD-box helicase 5 [Source:HGNC Symbol;Acc:HGNC:2746]","synonyms":"p68,HLR1,G17P1","biotype":"protein_coding","ncbi_id":"1655","summary":"This gene encodes a member of the DEAD box family of RNA helicases that are involved in a variety of cellular processes as a result of its role as an adaptor molecule, promoting interactions with a large number of other factors. This protein is involved in pathways that include the alteration of RNA structures, plays a role as a coregulator of transcription, a regulator of splicing, and in the processing of small noncoding RNAs. Members of this family contain nine conserved motifs, including the conserved Asp-Glu-Ala-Asp (DEAD) motif, important to ATP binding and hydrolysis as well as RNA binding and unwinding activities. Dysregulation of this gene may play a role in cancer development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2017]","start":64499616,"end":64508199,"strand":-1,"description":"DEAD-box helicase 5 [Source:HGNC Symbol;Acc:HGNC:2746]"}, {"versioned_ensembl_gene_id":"ENSG00000205790.1","gene_symbol":"DPP9-AS1","gene_name":"DPP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50706]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131094","summary":null,"start":4679282,"end":4685948,"strand":1,"description":"DPP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50706]"}, {"versioned_ensembl_gene_id":"ENSG00000224625.2","gene_symbol":"TUBB8P6","gene_name":"tubulin beta 8 class VIII pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42343]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"200149","summary":null,"start":242057085,"end":242060242,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42343]"}, {"versioned_ensembl_gene_id":"ENSG00000236515.3","gene_symbol":"ZBTB9","gene_name":"zinc finger and BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28323]","synonyms":"ZNF919,MGC23166","biotype":"protein_coding","ncbi_id":"221504","summary":null,"start":33594767,"end":33597736,"strand":1,"description":"zinc finger and BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28323]"}, {"versioned_ensembl_gene_id":"ENSG00000260067.1","gene_symbol":"MTND4LP25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42259]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075243","summary":null,"start":49066567,"end":49066729,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42259]"}, {"versioned_ensembl_gene_id":"ENSG00000263863.1","gene_symbol":"AC007948.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65105873,"end":65125710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134242.15","gene_symbol":"PTPN22","gene_name":"protein tyrosine phosphatase, non-receptor type 22 [Source:HGNC Symbol;Acc:HGNC:9652]","synonyms":"Lyp1,Lyp,PTPN8,Lyp2","biotype":"protein_coding","ncbi_id":"26191","summary":"This gene encodes of member of the non-receptor class 4 subfamily of the protein-tyrosine phosphatase family. The encoded protein is a lymphoid-specific intracellular phosphatase that associates with the molecular adapter protein CBL and may be involved in regulating CBL function in the T-cell receptor signaling pathway. Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes, rheumatoid arthritis, systemic lupus erythematosus and Graves' disease. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Mar 2009]","start":113813811,"end":113871759,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 22 [Source:HGNC Symbol;Acc:HGNC:9652]"}, {"versioned_ensembl_gene_id":"ENSG00000249335.1","gene_symbol":"AC093523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68832585,"end":68962158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249588.1","gene_symbol":"AC010280.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68523878,"end":68530007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255197.5","gene_symbol":"AC090559.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47383148,"end":47409190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254369.6","gene_symbol":"HOXA-AS3","gene_name":"HOXA cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:43748]","synonyms":"HOXA6as","biotype":"antisense_RNA","ncbi_id":"100133311","summary":null,"start":27129977,"end":27155928,"strand":1,"description":"HOXA cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:43748]"}, {"versioned_ensembl_gene_id":"ENSG00000269190.5","gene_symbol":"FBXO17","gene_name":"F-box protein 17 [Source:HGNC Symbol;Acc:HGNC:18754]","synonyms":"MGC9379,FLJ25205,FLJ11798,FBXO26,Fbx17,FBG4","biotype":"protein_coding","ncbi_id":"115290","summary":"This gene encodes a member of the F-box protein family which is characterized by the F-box motif. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it contains an F-box domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":38941401,"end":38975910,"strand":-1,"description":"F-box protein 17 [Source:HGNC Symbol;Acc:HGNC:18754]"}, {"versioned_ensembl_gene_id":"ENSG00000279534.1","gene_symbol":"AP001340.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25371827,"end":25372043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236099.1","gene_symbol":"AC013403.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27158563,"end":27159229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251583.1","gene_symbol":"AC008427.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149932014,"end":149932668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205018.2","gene_symbol":"AC092384.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88939789,"end":88951524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261281.1","gene_symbol":"AC009712.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":72682266,"end":72682904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047597.5","gene_symbol":"XK","gene_name":"X-linked Kx blood group [Source:HGNC Symbol;Acc:HGNC:12811]","synonyms":"NA,Kx,XKR1,X1k,NAC","biotype":"protein_coding","ncbi_id":"7504","summary":"This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]","start":37685759,"end":37732130,"strand":1,"description":"X-linked Kx blood group [Source:HGNC Symbol;Acc:HGNC:12811]"}, {"versioned_ensembl_gene_id":"ENSG00000229735.1","gene_symbol":"FTLP16","gene_name":"ferritin light chain pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37966]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420158","summary":null,"start":38484752,"end":38485264,"strand":-1,"description":"ferritin light chain pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37966]"}, {"versioned_ensembl_gene_id":"ENSG00000171067.10","gene_symbol":"C11orf24","gene_name":"chromosome 11 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:1174]","synonyms":"DM4E3","biotype":"protein_coding","ncbi_id":"53838","summary":null,"start":68261335,"end":68272001,"strand":-1,"description":"chromosome 11 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:1174]"}, {"versioned_ensembl_gene_id":"ENSG00000261124.1","gene_symbol":"AC135050.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31065495,"end":31069246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232035.1","gene_symbol":"AL135790.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10631750,"end":10632203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159289.6","gene_symbol":"GOLGA6A","gene_name":"golgin A6 family member A [Source:HGNC Symbol;Acc:HGNC:13567]","synonyms":"GOLGA6,GLP","biotype":"protein_coding","ncbi_id":"342096","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes. [provided by RefSeq, Jul 2008]","start":74069857,"end":74082550,"strand":-1,"description":"golgin A6 family member A [Source:HGNC Symbol;Acc:HGNC:13567]"}, {"versioned_ensembl_gene_id":"ENSG00000248366.1","gene_symbol":"TRAJ51","gene_name":"T-cell receptor alpha joining 51 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12083]","synonyms":null,"biotype":"TR_J_pseudogene","ncbi_id":"28704","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22487183,"end":22487245,"strand":1,"description":"T-cell receptor alpha joining 51 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12083]"}, {"versioned_ensembl_gene_id":"ENSG00000234612.1","gene_symbol":"H2AFZP5","gene_name":"H2A histone family member Z pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288330","summary":null,"start":77953495,"end":77953876,"strand":1,"description":"H2A histone family member Z pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38018]"}, {"versioned_ensembl_gene_id":"ENSG00000110660.14","gene_symbol":"SLC35F2","gene_name":"solute carrier family 35 member F2 [Source:HGNC Symbol;Acc:HGNC:23615]","synonyms":"FLJ13018","biotype":"protein_coding","ncbi_id":"54733","summary":null,"start":107790991,"end":107928293,"strand":-1,"description":"solute carrier family 35 member F2 [Source:HGNC Symbol;Acc:HGNC:23615]"}, {"versioned_ensembl_gene_id":"ENSG00000162814.10","gene_symbol":"SPATA17","gene_name":"spermatogenesis associated 17 [Source:HGNC Symbol;Acc:HGNC:25184]","synonyms":"IQCH","biotype":"protein_coding","ncbi_id":"128153","summary":null,"start":217631324,"end":217871696,"strand":1,"description":"spermatogenesis associated 17 [Source:HGNC Symbol;Acc:HGNC:25184]"}, {"versioned_ensembl_gene_id":"ENSG00000234223.2","gene_symbol":"AC003988.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80246409,"end":80312456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272573.5","gene_symbol":"MUSTN1","gene_name":"musculoskeletal, embryonic nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:22144]","synonyms":"Mustang","biotype":"protein_coding","ncbi_id":"389125","summary":null,"start":52833114,"end":52835219,"strand":-1,"description":"musculoskeletal, embryonic nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:22144]"}, {"versioned_ensembl_gene_id":"ENSG00000004660.14","gene_symbol":"CAMKK1","gene_name":"calcium/calmodulin dependent protein kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:1469]","synonyms":"CAMKKA,MGC34095,DKFZp761M0423","biotype":"protein_coding","ncbi_id":"84254","summary":"The product of this gene belongs to the Serine/Threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. This protein plays a role in the calcium/calmodulin-dependent (CaM) kinase cascade. Three transcript variants encoding two distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":3860315,"end":3894891,"strand":-1,"description":"calcium/calmodulin dependent protein kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:1469]"}, {"versioned_ensembl_gene_id":"ENSG00000281357.2","gene_symbol":"ARRDC3-AS1","gene_name":"ARRDC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44145]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129716","summary":null,"start":91380349,"end":91439085,"strand":1,"description":"ARRDC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44145]"}, {"versioned_ensembl_gene_id":"ENSG00000237579.2","gene_symbol":"LINC01514","gene_name":"long intergenic non-protein coding RNA 1514 [Source:HGNC Symbol;Acc:HGNC:51207]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927396","summary":null,"start":101176323,"end":101194147,"strand":1,"description":"long intergenic non-protein coding RNA 1514 [Source:HGNC Symbol;Acc:HGNC:51207]"}, {"versioned_ensembl_gene_id":"ENSG00000270973.1","gene_symbol":"SMARCE1P7","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51208]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481716","summary":null,"start":101181144,"end":101181951,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51208]"}, {"versioned_ensembl_gene_id":"ENSG00000225564.6","gene_symbol":"LINC01492","gene_name":"long intergenic non-protein coding RNA 1492 [Source:HGNC Symbol;Acc:HGNC:51149]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928496","summary":null,"start":103140523,"end":103325034,"strand":-1,"description":"long intergenic non-protein coding RNA 1492 [Source:HGNC Symbol;Acc:HGNC:51149]"}, {"versioned_ensembl_gene_id":"ENSG00000232617.1","gene_symbol":"AC017019.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9665229,"end":9669010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180329.13","gene_symbol":"CCDC43","gene_name":"coiled-coil domain containing 43 [Source:HGNC Symbol;Acc:HGNC:26472]","synonyms":"FLJ31795","biotype":"protein_coding","ncbi_id":"124808","summary":null,"start":44673069,"end":44689779,"strand":-1,"description":"coiled-coil domain containing 43 [Source:HGNC Symbol;Acc:HGNC:26472]"}, {"versioned_ensembl_gene_id":"ENSG00000133835.14","gene_symbol":"HSD17B4","gene_name":"hydroxysteroid 17-beta dehydrogenase 4 [Source:HGNC Symbol;Acc:HGNC:5213]","synonyms":"SDR8C1,MFE-2,DBP","biotype":"protein_coding","ncbi_id":"3295","summary":"The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":119452443,"end":119637199,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 4 [Source:HGNC Symbol;Acc:HGNC:5213]"}, {"versioned_ensembl_gene_id":"ENSG00000241059.2","gene_symbol":"AC008799.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91355380,"end":91356026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158050.4","gene_symbol":"DUSP2","gene_name":"dual specificity phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3068]","synonyms":"PAC-1","biotype":"protein_coding","ncbi_id":"1844","summary":" The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates ERK1 and ERK2, is predominantly expressed in hematopoietic tissues, and is localized in the nucleus. [provided by RefSeq, Jul 2008]","start":96143166,"end":96145440,"strand":-1,"description":"dual specificity phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3068]"}, {"versioned_ensembl_gene_id":"ENSG00000206034.1","gene_symbol":"DEFB109B","gene_name":"defensin beta 109B [Source:HGNC Symbol;Acc:HGNC:33469]","synonyms":"DEFB109P1B","biotype":"unprocessed_pseudogene","ncbi_id":"641517","summary":null,"start":7312846,"end":7319951,"strand":1,"description":"defensin beta 109B [Source:HGNC Symbol;Acc:HGNC:33469]"}, {"versioned_ensembl_gene_id":"ENSG00000139438.5","gene_symbol":"FAM222A","gene_name":"family with sequence similarity 222 member A [Source:HGNC Symbol;Acc:HGNC:25915]","synonyms":"C12orf34,FLJ14721","biotype":"protein_coding","ncbi_id":"84915","summary":null,"start":109714228,"end":109770507,"strand":1,"description":"family with sequence similarity 222 member A [Source:HGNC Symbol;Acc:HGNC:25915]"}, {"versioned_ensembl_gene_id":"ENSG00000041515.15","gene_symbol":"MYO16","gene_name":"myosin XVI [Source:HGNC Symbol;Acc:HGNC:29822]","synonyms":"NYAP3,MYR8,Myo16b,KIAA0865,PPP1R107","biotype":"protein_coding","ncbi_id":"23026","summary":"This gene encodes an unconventional myosin protein. The encoded protein has been proposed to act as a serine/threonine phosphatase-1 targeting or regulatory subunit. Studies in a rat cell line suggest that this protein may regulate cell cycle progression. A variant within this gene may be associated with susceptibility to schizophrenia and elevated expression of this gene has been observed in the frontal cortex of human schizophrenia patients. [provided by RefSeq, Mar 2017]","start":108596152,"end":109208007,"strand":1,"description":"myosin XVI [Source:HGNC Symbol;Acc:HGNC:29822]"}, {"versioned_ensembl_gene_id":"ENSG00000183828.14","gene_symbol":"NUDT14","gene_name":"nudix hydrolase 14 [Source:HGNC Symbol;Acc:HGNC:20141]","synonyms":"UGPP","biotype":"protein_coding","ncbi_id":"256281","summary":"The protein encoded by this gene is a member of the Nudix hydrolase family. Nudix hydrolases eliminate potentially toxic nucleotide metabolites from the cell and regulate the concentrations and availability of many different nucleotide substrates, cofactors, and signaling molecules. This enzyme contains a Nudix hydrolase domain and is a UDPG pyrophosphatase that hydrolyzes UDPG to produce glucose 1-phosphate and UMP. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":105172938,"end":105181323,"strand":-1,"description":"nudix hydrolase 14 [Source:HGNC Symbol;Acc:HGNC:20141]"}, {"versioned_ensembl_gene_id":"ENSG00000260672.1","gene_symbol":"AC100827.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72615810,"end":72618250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106689.10","gene_symbol":"LHX2","gene_name":"LIM homeobox 2 [Source:HGNC Symbol;Acc:HGNC:6594]","synonyms":"LH-2,hLhx2","biotype":"protein_coding","ncbi_id":"9355","summary":"This gene encodes a protein belonging to a large protein family, members of which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator. The protein can recapitulate or rescue phenotypes in Drosophila caused by a related protein, suggesting conservation of function during evolution. [provided by RefSeq, Jul 2008]","start":124001670,"end":124033301,"strand":1,"description":"LIM homeobox 2 [Source:HGNC Symbol;Acc:HGNC:6594]"}, {"versioned_ensembl_gene_id":"ENSG00000279299.1","gene_symbol":"AP000648.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90125658,"end":90126061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141026.5","gene_symbol":"MED9","gene_name":"mediator complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:25487]","synonyms":"MED25,FLJ10193","biotype":"protein_coding","ncbi_id":"55090","summary":"The multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":17476986,"end":17493226,"strand":1,"description":"mediator complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:25487]"}, {"versioned_ensembl_gene_id":"ENSG00000129292.20","gene_symbol":"PHF20L1","gene_name":"PHD finger protein 20 like 1 [Source:HGNC Symbol;Acc:HGNC:24280]","synonyms":"TDRD20B,MGC64923,FLJ21615,FLJ13649,CGI-72","biotype":"protein_coding","ncbi_id":"51105","summary":null,"start":132775358,"end":132848807,"strand":1,"description":"PHD finger protein 20 like 1 [Source:HGNC Symbol;Acc:HGNC:24280]"}, {"versioned_ensembl_gene_id":"ENSG00000232771.2","gene_symbol":"PPP1R26P5","gene_name":"protein phosphatase 1 regulatory subunit 26 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42019]","synonyms":"KIAA0649P5","biotype":"processed_pseudogene","ncbi_id":"100133040","summary":null,"start":21341595,"end":21345258,"strand":1,"description":"protein phosphatase 1 regulatory subunit 26 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42019]"}, {"versioned_ensembl_gene_id":"ENSG00000241416.1","gene_symbol":"KRT8P13","gene_name":"keratin 8 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:33365]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730023","summary":null,"start":170495627,"end":170496636,"strand":1,"description":"keratin 8 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:33365]"}, {"versioned_ensembl_gene_id":"ENSG00000211836.1","gene_symbol":"TRAJ54","gene_name":"T-cell receptor alpha joining 54 [Source:HGNC Symbol;Acc:HGNC:12086]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28701","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22482287,"end":22482346,"strand":1,"description":"T-cell receptor alpha joining 54 [Source:HGNC Symbol;Acc:HGNC:12086]"}, {"versioned_ensembl_gene_id":"ENSG00000283234.1","gene_symbol":"AL590556.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":21950679,"end":21956871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167711.13","gene_symbol":"SERPINF2","gene_name":"serpin family F member 2 [Source:HGNC Symbol;Acc:HGNC:9075]","synonyms":"PLI,API,ALPHA-2-PI,AAP,A2AP","biotype":"protein_coding","ncbi_id":"5345","summary":"This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":1742836,"end":1755268,"strand":1,"description":"serpin family F member 2 [Source:HGNC Symbol;Acc:HGNC:9075]"}, {"versioned_ensembl_gene_id":"ENSG00000237899.1","gene_symbol":"AL031289.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40669089,"end":40687588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241667.1","gene_symbol":"AC104445.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69591341,"end":69593121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255587.7","gene_symbol":"RAB44","gene_name":"RAB44, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:21068]","synonyms":"RASL13,RASD3,dJ431A14.3","biotype":"protein_coding","ncbi_id":"401258","summary":null,"start":36697851,"end":36733183,"strand":1,"description":"RAB44, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:21068]"}, {"versioned_ensembl_gene_id":"ENSG00000235376.5","gene_symbol":"RPEL1","gene_name":"ribulose-5-phosphate-3-epimerase like 1 [Source:HGNC Symbol;Acc:HGNC:45241]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729020","summary":null,"start":103245887,"end":103248016,"strand":1,"description":"ribulose-5-phosphate-3-epimerase like 1 [Source:HGNC Symbol;Acc:HGNC:45241]"}, {"versioned_ensembl_gene_id":"ENSG00000248191.1","gene_symbol":"PES1P1","gene_name":"pescadillo ribosomal biogenesis factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44058]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"345016","summary":null,"start":134327063,"end":134328798,"strand":1,"description":"pescadillo ribosomal biogenesis factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44058]"}, {"versioned_ensembl_gene_id":"ENSG00000245466.1","gene_symbol":"AL357153.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70608798,"end":70641298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234626.1","gene_symbol":"AL021937.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32327171,"end":32343105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237733.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"LIRF,HZFw1","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30065423,"end":30071044,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000227429.5","gene_symbol":"HCP5","gene_name":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]","synonyms":"P5-1,D6S2650E","biotype":"processed_transcript","ncbi_id":"10866","summary":null,"start":31540726,"end":31542189,"strand":1,"description":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]"}, {"versioned_ensembl_gene_id":"ENSG00000196345.12","gene_symbol":"ZKSCAN7","gene_name":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]","synonyms":"ZSCAN39,ZNF64,ZNF448,ZNF167,FLJ12738","biotype":"protein_coding","ncbi_id":"55888","summary":null,"start":44555193,"end":44594173,"strand":1,"description":"zinc finger with KRAB and SCAN domains 7 [Source:HGNC Symbol;Acc:HGNC:12955]"}, {"versioned_ensembl_gene_id":"ENSG00000227920.2","gene_symbol":"AL353597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37545145,"end":37550860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223822.2","gene_symbol":"EEF1A1P1","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3191]","synonyms":"EEF1A1P","biotype":"processed_pseudogene","ncbi_id":"54054","summary":null,"start":23390258,"end":23390996,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3191]"}, {"versioned_ensembl_gene_id":"ENSG00000233509.2","gene_symbol":"ZNF197-AS1","gene_name":"ZNF197 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40620]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874094","summary":null,"start":44617128,"end":44624797,"strand":-1,"description":"ZNF197 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40620]"}, {"versioned_ensembl_gene_id":"ENSG00000249467.1","gene_symbol":"AL592156.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36719918,"end":36720221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070761.7","gene_symbol":"CFAP20","gene_name":"cilia and flagella associated protein 20 [Source:HGNC Symbol;Acc:HGNC:29523]","synonyms":"GTL3,fSAP23,C16orf80","biotype":"protein_coding","ncbi_id":"29105","summary":null,"start":58113588,"end":58129450,"strand":-1,"description":"cilia and flagella associated protein 20 [Source:HGNC Symbol;Acc:HGNC:29523]"}, {"versioned_ensembl_gene_id":"ENSG00000219608.3","gene_symbol":"HIGD1AP16","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:43011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874476","summary":null,"start":35878476,"end":35878733,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:43011]"}, {"versioned_ensembl_gene_id":"ENSG00000136514.2","gene_symbol":"RTP4","gene_name":"receptor transporter protein 4 [Source:HGNC Symbol;Acc:HGNC:23992]","synonyms":"Z3CXXC4,IFRG28","biotype":"protein_coding","ncbi_id":"64108","summary":null,"start":187368332,"end":187372076,"strand":1,"description":"receptor transporter protein 4 [Source:HGNC Symbol;Acc:HGNC:23992]"}, {"versioned_ensembl_gene_id":"ENSG00000283145.1","gene_symbol":"AP000550.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21228760,"end":21229138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185561.9","gene_symbol":"TLCD2","gene_name":"TLC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"727910","summary":null,"start":1702790,"end":1710438,"strand":-1,"description":"TLC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33522]"}, {"versioned_ensembl_gene_id":"ENSG00000231245.2","gene_symbol":"C1DP1","gene_name":"C1D nuclear receptor corepressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31465]","synonyms":"bA195O1.1","biotype":"processed_pseudogene","ncbi_id":"554049","summary":null,"start":32511336,"end":32511737,"strand":-1,"description":"C1D nuclear receptor corepressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31465]"}, {"versioned_ensembl_gene_id":"ENSG00000143319.16","gene_symbol":"ISG20L2","gene_name":"interferon stimulated exonuclease gene 20 like 2 [Source:HGNC Symbol;Acc:HGNC:25745]","synonyms":"FLJ12671","biotype":"protein_coding","ncbi_id":"81875","summary":"This gene encodes a 3'-5' exoribonuclease that may be involved in the processing of the 12S pre-rRNA. Pseudogenes have been identified on chromosomes 6 and 11. [provided by RefSeq, Dec 2014]","start":156721891,"end":156728799,"strand":-1,"description":"interferon stimulated exonuclease gene 20 like 2 [Source:HGNC Symbol;Acc:HGNC:25745]"}, {"versioned_ensembl_gene_id":"ENSG00000204197.9","gene_symbol":"KIFC1","gene_name":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]","synonyms":"KNSL2,HSET","biotype":"protein_coding","ncbi_id":"3833","summary":null,"start":33320351,"end":33338717,"strand":1,"description":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]"}, {"versioned_ensembl_gene_id":"ENSG00000214015.3","gene_symbol":"RPL32P23","gene_name":"ribosomal protein L32 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644020","summary":null,"start":6071514,"end":6071918,"strand":-1,"description":"ribosomal protein L32 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36007]"}, {"versioned_ensembl_gene_id":"ENSG00000255270.1","gene_symbol":"NAV2-IT1","gene_name":"NAV2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41416]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874305","summary":null,"start":19380484,"end":19385014,"strand":1,"description":"NAV2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41416]"}, {"versioned_ensembl_gene_id":"ENSG00000254622.1","gene_symbol":"NAV2-AS4","gene_name":"NAV2 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40741]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"399876","summary":null,"start":19510890,"end":19519896,"strand":-1,"description":"NAV2 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40741]"}, {"versioned_ensembl_gene_id":"ENSG00000133475.17","gene_symbol":"GGT2","gene_name":"gamma-glutamyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4251]","synonyms":"GGT","biotype":"protein_coding","ncbi_id":"728441","summary":"GGT2 belongs to the gamma-glutamyltransferase (GGT; EC 2.3.2.2) gene family. GGT is a membrane-bound extracellular enzyme that cleaves gamma-glutamyl peptide bonds in glutathione and other peptides and transfers the gamma-glutamyl moiety to acceptors. GGT is also key to glutathione homeostasis because it provides substrates for glutathione synthesis (Heisterkamp et al., 2008 [PubMed 18357469]).[supplied by OMIM, Oct 2008]","start":21207973,"end":21227637,"strand":-1,"description":"gamma-glutamyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4251]"}, {"versioned_ensembl_gene_id":"ENSG00000228410.6","gene_symbol":"ELOCP24","gene_name":"elongin C pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:38160]","synonyms":"TCEB1P25,TCEB1P24","biotype":"processed_pseudogene","ncbi_id":"100287692","summary":null,"start":155978992,"end":155979325,"strand":-1,"description":"elongin C pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:38160]"}, {"versioned_ensembl_gene_id":"ENSG00000233215.5","gene_symbol":"LINC01687","gene_name":"long intergenic non-protein coding RNA 1687 [Source:HGNC Symbol;Acc:HGNC:52474]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927843","summary":null,"start":22008944,"end":22098459,"strand":-1,"description":"long intergenic non-protein coding RNA 1687 [Source:HGNC Symbol;Acc:HGNC:52474]"}, {"versioned_ensembl_gene_id":"ENSG00000264911.1","gene_symbol":"AC022069.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26348347,"end":26349004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101265.15","gene_symbol":"RASSF2","gene_name":"Ras association domain family member 2 [Source:HGNC Symbol;Acc:HGNC:9883]","synonyms":"KIAA0168,CENP-34","biotype":"protein_coding","ncbi_id":"9770","summary":"This gene encodes a protein that contains a Ras association domain. Similar to its cattle and sheep counterparts, this gene is located near the prion gene. Two alternatively spliced transcripts encoding the same isoform have been reported. [provided by RefSeq, Jul 2008]","start":4780023,"end":4823645,"strand":-1,"description":"Ras association domain family member 2 [Source:HGNC Symbol;Acc:HGNC:9883]"}, {"versioned_ensembl_gene_id":"ENSG00000148908.14","gene_symbol":"RGS10","gene_name":"regulator of G protein signaling 10 [Source:HGNC Symbol;Acc:HGNC:9992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6001","summary":"Regulator of G protein signaling (RGS) family members are regulatory molecules that act as GTPase activating proteins (GAPs) for G alpha subunits of heterotrimeric G proteins. RGS proteins are able to deactivate G protein subunits of the Gi alpha, Go alpha and Gq alpha subtypes. They drive G proteins into their inactive GDP-bound forms. Regulator of G protein signaling 10 belongs to this family. All RGS proteins share a conserved 120-amino acid sequence termed the RGS domain. This protein associates specifically with the activated forms of the two related G-protein subunits, G-alphai3 and G-alphaz but fails to interact with the structurally and functionally distinct G-alpha subunits. Regulator of G protein signaling 10 protein is localized in the nucleus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":119499828,"end":119542708,"strand":-1,"description":"regulator of G protein signaling 10 [Source:HGNC Symbol;Acc:HGNC:9992]"}, {"versioned_ensembl_gene_id":"ENSG00000229877.1","gene_symbol":"PAICSP5","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38098]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780811","summary":null,"start":143545186,"end":143546735,"strand":-1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38098]"}, {"versioned_ensembl_gene_id":"ENSG00000237258.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425047,"end":29456602,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000283537.1","gene_symbol":"AC073264.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143623776,"end":143624398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260246.1","gene_symbol":"AC000032.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109693117,"end":109693742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237551.1","gene_symbol":"AC096775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96283357,"end":96283804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166352.15","gene_symbol":"C11orf74","gene_name":"chromosome 11 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:25142]","synonyms":"FLJ38678,NWC,HEPIS","biotype":"protein_coding","ncbi_id":"119710","summary":"This gene encodes a protein that was identified as a cellular interacting partner of non-structural protein 10 of the severe acute respiratory syndrome coronavirus (SARS-CoV). The encoded protein may function as a negative regulator of transcription. There is a pseudogene for this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":36594493,"end":36659290,"strand":1,"description":"chromosome 11 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:25142]"}, {"versioned_ensembl_gene_id":"ENSG00000167680.15","gene_symbol":"SEMA6B","gene_name":"semaphorin 6B [Source:HGNC Symbol;Acc:HGNC:10739]","synonyms":"semaZ,SEMAN,SEMA-VIB,SEM-SEMA-Y","biotype":"protein_coding","ncbi_id":"10501","summary":"This gene encodes a member of the semaphorin family, a group of proteins characterized by the presence of a conserved semaphorin (sema) domain. Whereas some semaphorins are transmembrane proteins, others are secreted. Semaphorins play a major role in axon guidance. The protein encoded by this gene may be involved in both peripheral and central nervous system development. [provided by RefSeq, Jul 2008]","start":4542593,"end":4559808,"strand":-1,"description":"semaphorin 6B [Source:HGNC Symbol;Acc:HGNC:10739]"}, {"versioned_ensembl_gene_id":"ENSG00000279033.1","gene_symbol":"AC090984.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77484275,"end":77485606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055957.10","gene_symbol":"ITIH1","gene_name":"inter-alpha-trypsin inhibitor heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:6166]","synonyms":"ITIH,IATIH,H1P","biotype":"protein_coding","ncbi_id":"3697","summary":"This gene encodes a member of the inter-alpha-trypsin inhibitor family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the heavy chain of the inter-alpha-trypsin inhibitor complex, which is secreted by hepatocytes into the blood. The heavy chain also interacts with hyaluronan, and this interaction may play a role in ovulation and fertilization, and has been implicated in multiple inflammatory diseases. This gene is present in a gene cluster on chromosome 3. [provided by RefSeq, Nov 2015]","start":52777592,"end":52792068,"strand":1,"description":"inter-alpha-trypsin inhibitor heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:6166]"}, {"versioned_ensembl_gene_id":"ENSG00000198826.10","gene_symbol":"ARHGAP11A","gene_name":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]","synonyms":"KIAA0013,KIAA0013","biotype":"protein_coding","ncbi_id":"9824","summary":"This gene encodes a member of the Rho GTPase activating protein family. In response to DNA damage, the encoded protein interacts with the p53 tumor suppressor protein and stimulates its tetramerization, which results in cell-cycle arrest and apoptosis. A chromosomal deletion that includes this gene is one cause of Prader-Willi syndrome, and an intronic variant of this gene may be associated with sleep duration in children. This gene is highly expressed in colon cancers and in a human basal-like breast cancer cell line. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32615144,"end":32639949,"strand":1,"description":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]"}, {"versioned_ensembl_gene_id":"ENSG00000241052.1","gene_symbol":"RPL23AP70","gene_name":"ribosomal protein L23a pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:36030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271619","summary":null,"start":35144021,"end":35144480,"strand":-1,"description":"ribosomal protein L23a pseudogene 70 [Source:HGNC Symbol;Acc:HGNC:36030]"}, {"versioned_ensembl_gene_id":"ENSG00000230559.1","gene_symbol":"RPL17P12","gene_name":"ribosomal protein L17 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270938","summary":null,"start":146194296,"end":146194821,"strand":1,"description":"ribosomal protein L17 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36779]"}, {"versioned_ensembl_gene_id":"ENSG00000246662.6","gene_symbol":"LINC00535","gene_name":"long intergenic non-protein coding RNA 535 [Source:HGNC Symbol;Acc:HGNC:43644]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"642924","summary":null,"start":93213302,"end":93700433,"strand":-1,"description":"long intergenic non-protein coding RNA 535 [Source:HGNC Symbol;Acc:HGNC:43644]"}, {"versioned_ensembl_gene_id":"ENSG00000243284.1","gene_symbol":"VSIG8","gene_name":"V-set and immunoglobulin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:32063]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391123","summary":null,"start":159854316,"end":159862657,"strand":-1,"description":"V-set and immunoglobulin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:32063]"}, {"versioned_ensembl_gene_id":"ENSG00000275557.1","gene_symbol":"AC242842.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149607765,"end":149612402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259426.5","gene_symbol":"AC027237.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69396904,"end":69415029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105549.10","gene_symbol":"THEG","gene_name":"theg spermatid protein [Source:HGNC Symbol;Acc:HGNC:13706]","synonyms":"THEG1,CT56","biotype":"protein_coding","ncbi_id":"51298","summary":"This gene is specifically expressed in the nucleus of haploid male germ cells. The orthologous gene in mice encodes a protein that may play a role in protein assembly through interactions with T-complex protein 1 subunit epsilon. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":361747,"end":376670,"strand":-1,"description":"theg spermatid protein [Source:HGNC Symbol;Acc:HGNC:13706]"}, {"versioned_ensembl_gene_id":"ENSG00000054654.16","gene_symbol":"SYNE2","gene_name":"spectrin repeat containing nuclear envelope protein 2 [Source:HGNC Symbol;Acc:HGNC:17084]","synonyms":"NUANCE,NUA,Nesprin-2,Nesp2,KIAA1011,DKFZP434H2235,SYNE-2","biotype":"protein_coding","ncbi_id":"23224","summary":"The protein encoded by this gene is a nuclear outer membrane protein that binds cytoplasmic F-actin. This binding tethers the nucleus to the cytoskeleton and aids in the maintenance of the structural integrity of the nucleus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":63852983,"end":64226433,"strand":1,"description":"spectrin repeat containing nuclear envelope protein 2 [Source:HGNC Symbol;Acc:HGNC:17084]"}, {"versioned_ensembl_gene_id":"ENSG00000229154.1","gene_symbol":"KCNQ5-AS1","gene_name":"KCNQ5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40323]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873997","summary":null,"start":73134803,"end":73143514,"strand":-1,"description":"KCNQ5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40323]"}, {"versioned_ensembl_gene_id":"ENSG00000233524.1","gene_symbol":"RANP8","gene_name":"RAN, member RAS oncogene family pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420519","summary":null,"start":20747035,"end":20748057,"strand":-1,"description":"RAN, member RAS oncogene family pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39863]"}, {"versioned_ensembl_gene_id":"ENSG00000160094.14","gene_symbol":"ZNF362","gene_name":"zinc finger protein 362 [Source:HGNC Symbol;Acc:HGNC:18079]","synonyms":"RN,lin-29,FLJ25476","biotype":"protein_coding","ncbi_id":"149076","summary":null,"start":33256545,"end":33300719,"strand":1,"description":"zinc finger protein 362 [Source:HGNC Symbol;Acc:HGNC:18079]"}, {"versioned_ensembl_gene_id":"ENSG00000260304.1","gene_symbol":"AC009088.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31182511,"end":31183285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214870.8","gene_symbol":"AC004540.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26398593,"end":26494256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109771.15","gene_symbol":"LRP2BP","gene_name":"LRP2 binding protein [Source:HGNC Symbol;Acc:HGNC:25434]","synonyms":"DKFZp761O0113","biotype":"protein_coding","ncbi_id":"55805","summary":null,"start":185363879,"end":185395899,"strand":-1,"description":"LRP2 binding protein [Source:HGNC Symbol;Acc:HGNC:25434]"}, {"versioned_ensembl_gene_id":"ENSG00000232387.2","gene_symbol":"SKA2P1","gene_name":"spindle and kinetochore associated complex subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23122]","synonyms":"SKA2L,FAM33B,Em:AC006313.1","biotype":"processed_pseudogene","ncbi_id":"729012","summary":null,"start":122761844,"end":122762233,"strand":1,"description":"spindle and kinetochore associated complex subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23122]"}, {"versioned_ensembl_gene_id":"ENSG00000249267.6","gene_symbol":"LINC00939","gene_name":"long intergenic non-protein coding RNA 939 [Source:HGNC Symbol;Acc:HGNC:48631]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400084","summary":null,"start":125958688,"end":125983374,"strand":-1,"description":"long intergenic non-protein coding RNA 939 [Source:HGNC Symbol;Acc:HGNC:48631]"}, {"versioned_ensembl_gene_id":"ENSG00000130758.7","gene_symbol":"MAP3K10","gene_name":"mitogen-activated protein kinase kinase kinase 10 [Source:HGNC Symbol;Acc:HGNC:6849]","synonyms":"MST,MLK2,MEKK10","biotype":"protein_coding","ncbi_id":"4294","summary":"The protein encoded by this gene is a member of the serine/threonine kinase family. This kinase has been shown to activate MAPK8/JNK and MKK4/SEK1, and this kinase itself can be phoshorylated, and thus activated by JNK kinases. This kinase functions preferentially on the JNK signaling pathway, and is reported to be involved in nerve growth factor (NGF) induced neuronal apoptosis. [provided by RefSeq, Jul 2008]","start":40191744,"end":40215575,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 10 [Source:HGNC Symbol;Acc:HGNC:6849]"}, {"versioned_ensembl_gene_id":"ENSG00000246876.6","gene_symbol":"LINC02466","gene_name":"long intergenic non-protein coding RNA 2466 [Source:HGNC Symbol;Acc:HGNC:53405]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927282","summary":null,"start":129724171,"end":129771481,"strand":-1,"description":"long intergenic non-protein coding RNA 2466 [Source:HGNC Symbol;Acc:HGNC:53405]"}, {"versioned_ensembl_gene_id":"ENSG00000081181.7","gene_symbol":"ARG2","gene_name":"arginase 2 [Source:HGNC Symbol;Acc:HGNC:664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"384","summary":" Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exists (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type II isoform encoded by this gene, is located in the mitochondria and expressed in extra-hepatic tissues, especially kidney. The physiologic role of this isoform is poorly understood; it is thought to play a role in nitric oxide and polyamine metabolism. Transcript variants of the type II gene resulting from the use of alternative polyadenylation sites have been described. [provided by RefSeq, Jul 2008]","start":67619798,"end":67651720,"strand":1,"description":"arginase 2 [Source:HGNC Symbol;Acc:HGNC:664]"}, {"versioned_ensembl_gene_id":"ENSG00000168959.14","gene_symbol":"GRM5","gene_name":"glutamate metabotropic receptor 5 [Source:HGNC Symbol;Acc:HGNC:4597]","synonyms":"PPP1R86,MGLUR5,mGlu5,GPRC1E","biotype":"protein_coding","ncbi_id":"2915","summary":"This gene encodes a member of the G-protein coupled receptor 3 protein family. The encoded protein is a metabatropic glutamate receptor, whose signaling activates a phosphatidylinositol-calcium second messenger system. This protein may be involved in the regulation of neural network activity and synaptic plasticity. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. A pseudogene of this gene has been defined on chromosome 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":88504576,"end":89065945,"strand":-1,"description":"glutamate metabotropic receptor 5 [Source:HGNC Symbol;Acc:HGNC:4597]"}, {"versioned_ensembl_gene_id":"ENSG00000253800.1","gene_symbol":"AC090136.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64570913,"end":64571332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253750.1","gene_symbol":"AC090136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64554236,"end":64554475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105556.11","gene_symbol":"MIER2","gene_name":"MIER family member 2 [Source:HGNC Symbol;Acc:HGNC:29210]","synonyms":"KIAA1193","biotype":"protein_coding","ncbi_id":"54531","summary":null,"start":301444,"end":344815,"strand":-1,"description":"MIER family member 2 [Source:HGNC Symbol;Acc:HGNC:29210]"}, {"versioned_ensembl_gene_id":"ENSG00000230742.3","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"processed_transcript","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29422544,"end":29431896,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000226013.1","gene_symbol":"MRPS18BP1","gene_name":"mitochondrial ribosomal protein S18B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29741]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359762","summary":null,"start":216201635,"end":216201826,"strand":-1,"description":"mitochondrial ribosomal protein S18B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29741]"}, {"versioned_ensembl_gene_id":"ENSG00000204588.5","gene_symbol":"LINC01123","gene_name":"long intergenic non-protein coding RNA 1123 [Source:HGNC Symbol;Acc:HGNC:49269]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440894","summary":null,"start":109987063,"end":109996140,"strand":1,"description":"long intergenic non-protein coding RNA 1123 [Source:HGNC Symbol;Acc:HGNC:49269]"}, {"versioned_ensembl_gene_id":"ENSG00000227750.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"TAT-SF1-L,HTATSF1P,dJ1033B10.6","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33408140,"end":33410038,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000271088.1","gene_symbol":"AL161722.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35741600,"end":35744582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197171.6","gene_symbol":"AL672167.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29223973,"end":29292963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259095.1","gene_symbol":"GTF2IP22","gene_name":"general transcription factor IIi pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480347","summary":null,"start":20173632,"end":20173813,"strand":-1,"description":"general transcription factor IIi pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51734]"}, {"versioned_ensembl_gene_id":"ENSG00000189132.6","gene_symbol":"FAM47B","gene_name":"family with sequence similarity 47 member B [Source:HGNC Symbol;Acc:HGNC:26659]","synonyms":"FLJ35782","biotype":"protein_coding","ncbi_id":"170062","summary":null,"start":34942796,"end":34944915,"strand":1,"description":"family with sequence similarity 47 member B [Source:HGNC Symbol;Acc:HGNC:26659]"}, {"versioned_ensembl_gene_id":"ENSG00000196090.12","gene_symbol":"PTPRT","gene_name":"protein tyrosine phosphatase, receptor type T [Source:HGNC Symbol;Acc:HGNC:9682]","synonyms":"RPTPrho,KIAA0283","biotype":"protein_coding","ncbi_id":"11122","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP (MAM) domain, Ig-like and fibronectin type III-like repeats. The protein domain structure and the expression pattern of the mouse counterpart of this PTP suggest its roles in both signal transduction and cellular adhesion in the central nervous system. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]","start":42072752,"end":43189970,"strand":-1,"description":"protein tyrosine phosphatase, receptor type T [Source:HGNC Symbol;Acc:HGNC:9682]"}, {"versioned_ensembl_gene_id":"ENSG00000154473.17","gene_symbol":"BUB3","gene_name":"BUB3, mitotic checkpoint protein [Source:HGNC Symbol;Acc:HGNC:1151]","synonyms":"BUB3L","biotype":"protein_coding","ncbi_id":"9184","summary":"This gene encodes a protein involved in spindle checkpoint function. The encoded protein contains four WD repeat domains and has sequence similarity with the yeast BUB3 protein. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":123154277,"end":123170467,"strand":1,"description":"BUB3, mitotic checkpoint protein [Source:HGNC Symbol;Acc:HGNC:1151]"}, {"versioned_ensembl_gene_id":"ENSG00000270477.1","gene_symbol":"AL033523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3693923,"end":3694075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158161.15","gene_symbol":"EYA3","gene_name":"EYA transcriptional coactivator and phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3521]","synonyms":"DKFZp686C132","biotype":"protein_coding","ncbi_id":"2140","summary":"This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator and have a role during development. It can act as a mediator of chemoresistance and cell survival in Ewing sarcoma cells, where this gene is up-regulated via a micro-RNA that binds to the 3' UTR of the transcript. A similar protein in mice acts as a transcriptional activator. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":27970344,"end":28088696,"strand":-1,"description":"EYA transcriptional coactivator and phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:3521]"}, {"versioned_ensembl_gene_id":"ENSG00000242660.1","gene_symbol":"AC015911.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35566517,"end":35566672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218813.1","gene_symbol":"AL354719.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63797189,"end":63798031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257648.1","gene_symbol":"CYCSP30","gene_name":"cytochrome c, somatic pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:24405]","synonyms":"HCP30","biotype":"processed_pseudogene","ncbi_id":"121026","summary":null,"start":87750142,"end":87750313,"strand":1,"description":"cytochrome c, somatic pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:24405]"}, {"versioned_ensembl_gene_id":"ENSG00000258899.1","gene_symbol":"OR4U1P","gene_name":"olfactory receptor family 4 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15361]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390434","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20043916,"end":20044827,"strand":1,"description":"olfactory receptor family 4 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15361]"}, {"versioned_ensembl_gene_id":"ENSG00000155761.13","gene_symbol":"SPAG17","gene_name":"sperm associated antigen 17 [Source:HGNC Symbol;Acc:HGNC:26620]","synonyms":"RP4-776P7.2,PF6,FLJ34497,CT143","biotype":"protein_coding","ncbi_id":"200162","summary":"This gene encodes a central pair protein present in the axonemes of cells with a \"9 + 2\" organization of microtubules. The encoded protein is required for the proper function of the axoneme. Mutations in the orthologous gene in mice lead to primary ciliary dyskinesia characterized by immotile nasal and tracheal cilia, reduced clearance of nasal mucus, profound respiratory distress, hydrocephalus, and neonatal lethality within twelve hours of birth due to impaired airway mucociliary clearance. Single-nucleotide polymorphisms in this gene are associated with human height and targeted mutations lead to skeletal malformations affecting the limbs in mice, suggesting a role for this gene in skeletal development. [provided by RefSeq, Feb 2017]","start":117953861,"end":118185223,"strand":-1,"description":"sperm associated antigen 17 [Source:HGNC Symbol;Acc:HGNC:26620]"}, {"versioned_ensembl_gene_id":"ENSG00000271551.2","gene_symbol":"AL355297.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156776360,"end":156778422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266312.1","gene_symbol":"LINC01927","gene_name":"long intergenic non-protein coding RNA 1927 [Source:HGNC Symbol;Acc:HGNC:52749]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927651","summary":null,"start":76623006,"end":76639011,"strand":-1,"description":"long intergenic non-protein coding RNA 1927 [Source:HGNC Symbol;Acc:HGNC:52749]"}, {"versioned_ensembl_gene_id":"ENSG00000203972.9","gene_symbol":"GLYATL3","gene_name":"glycine-N-acyltransferase like 3 [Source:HGNC Symbol;Acc:HGNC:21349]","synonyms":"C6orf140,bA28H17.2","biotype":"protein_coding","ncbi_id":"389396","summary":null,"start":49499958,"end":49527047,"strand":1,"description":"glycine-N-acyltransferase like 3 [Source:HGNC Symbol;Acc:HGNC:21349]"}, {"versioned_ensembl_gene_id":"ENSG00000176882.5","gene_symbol":"AL135901.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49620314,"end":49620646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167825.3","gene_symbol":"OR5I1","gene_name":"olfactory receptor family 5 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:8347]","synonyms":"OLF1,HSOlf1","biotype":"protein_coding","ncbi_id":"10798","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55935456,"end":55936400,"strand":-1,"description":"olfactory receptor family 5 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:8347]"}, {"versioned_ensembl_gene_id":"ENSG00000173678.14","gene_symbol":"SPDYE2B","gene_name":"speedy/RINGO cell cycle regulator family member E2B [Source:HGNC Symbol;Acc:HGNC:48334]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100310812","summary":null,"start":102650325,"end":102661398,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E2B [Source:HGNC Symbol;Acc:HGNC:48334]"}, {"versioned_ensembl_gene_id":"ENSG00000205611.4","gene_symbol":"LINC01597","gene_name":"long intergenic non-protein coding RNA 1597 [Source:HGNC Symbol;Acc:HGNC:51594]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400841","summary":null,"start":30278906,"end":30288479,"strand":-1,"description":"long intergenic non-protein coding RNA 1597 [Source:HGNC Symbol;Acc:HGNC:51594]"}, {"versioned_ensembl_gene_id":"ENSG00000050405.13","gene_symbol":"LIMA1","gene_name":"LIM domain and actin binding 1 [Source:HGNC Symbol;Acc:HGNC:24636]","synonyms":"EPLIN","biotype":"protein_coding","ncbi_id":"51474","summary":"This gene encodes a cytoskeleton-associated protein that inhibits actin filament depolymerization and cross-links filaments in bundles. It is downregulated in some cancer cell lines. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and expression of some of the variants maybe independently regulated. [provided by RefSeq, Aug 2011]","start":50175788,"end":50283546,"strand":-1,"description":"LIM domain and actin binding 1 [Source:HGNC Symbol;Acc:HGNC:24636]"}, {"versioned_ensembl_gene_id":"ENSG00000147592.8","gene_symbol":"LACTB2","gene_name":"lactamase beta 2 [Source:HGNC Symbol;Acc:HGNC:18512]","synonyms":"CGI-83","biotype":"protein_coding","ncbi_id":"51110","summary":null,"start":70635318,"end":70669174,"strand":-1,"description":"lactamase beta 2 [Source:HGNC Symbol;Acc:HGNC:18512]"}, {"versioned_ensembl_gene_id":"ENSG00000184702.18","gene_symbol":"SEPT5","gene_name":"septin 5 [Source:HGNC Symbol;Acc:HGNC:9164]","synonyms":"PNUTL1,HCDCREL-1,H5","biotype":"protein_coding","ncbi_id":"5413","summary":"This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. [provided by RefSeq, Dec 2010]","start":19714464,"end":19724772,"strand":1,"description":"septin 5 [Source:HGNC Symbol;Acc:HGNC:9164]"}, {"versioned_ensembl_gene_id":"ENSG00000282968.1","gene_symbol":"AGGF1P10","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51747]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288774","summary":null,"start":29430723,"end":29432913,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51747]"}, {"versioned_ensembl_gene_id":"ENSG00000262566.1","gene_symbol":"AL355375.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62611153,"end":62611327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228363.2","gene_symbol":"AC015971.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86562070,"end":86618766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248634.1","gene_symbol":"AC008588.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":128663978,"end":128742829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267184.1","gene_symbol":"AC002545.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69707193,"end":69707373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249884.8","gene_symbol":"RNF103-CHMP3","gene_name":"RNF103-CHMP3 readthrough [Source:HGNC Symbol;Acc:HGNC:38847]","synonyms":"RNF103-VPS24","biotype":"protein_coding","ncbi_id":"100526767","summary":"This locus represents naturally occurring read-through transcription between the neighboring RNF103 (ring finger protein 103) and CHMP3 (charged multivesicular body protein 3) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Oct 2011]","start":86505668,"end":86721122,"strand":-1,"description":"RNF103-CHMP3 readthrough [Source:HGNC Symbol;Acc:HGNC:38847]"}, {"versioned_ensembl_gene_id":"ENSG00000099364.16","gene_symbol":"FBXL19","gene_name":"F-box and leucine rich repeat protein 19 [Source:HGNC Symbol;Acc:HGNC:25300]","synonyms":"JHDM1C,Fbl19,DKFZp434K0410,CXXC11","biotype":"protein_coding","ncbi_id":"54620","summary":"This gene encodes a member of the Skp1-Cullin-F-box family of E3 ubiquitin ligases. The encoded protein is reported to bind to the transmembrane receptor interleukin 1 receptor-like 1 and regulate its ubiquitination and degradation. This protein has been linked to the regulation of pulmonary inflammation and psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":30923055,"end":30948783,"strand":1,"description":"F-box and leucine rich repeat protein 19 [Source:HGNC Symbol;Acc:HGNC:25300]"}, {"versioned_ensembl_gene_id":"ENSG00000260852.1","gene_symbol":"FBXL19-AS1","gene_name":"FBXL19 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27557]","synonyms":"NCRNA00095,MGC125472,MGC125470,MGC125469","biotype":"antisense_RNA","ncbi_id":"283932","summary":null,"start":30919319,"end":30923269,"strand":-1,"description":"FBXL19 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27557]"}, {"versioned_ensembl_gene_id":"ENSG00000255022.1","gene_symbol":"AP000676.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87816224,"end":87816524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254650.1","gene_symbol":"MTCYBP41","gene_name":"mitochondrially encoded cytochrome b pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52309]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729118","summary":null,"start":87815035,"end":87816157,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52309]"}, {"versioned_ensembl_gene_id":"ENSG00000106328.9","gene_symbol":"FSCN3","gene_name":"fascin actin-bundling protein 3 [Source:HGNC Symbol;Acc:HGNC:3961]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29999","summary":null,"start":127591409,"end":127602144,"strand":1,"description":"fascin actin-bundling protein 3 [Source:HGNC Symbol;Acc:HGNC:3961]"}, {"versioned_ensembl_gene_id":"ENSG00000271418.1","gene_symbol":"AC092747.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27093923,"end":27094223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278458.4","gene_symbol":"KANSL1","gene_name":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]","synonyms":"MSL1v1,MSL1v1,KIAA1267,KIAA1267,DKFZP727C091,DKFZP727C091,CENP-36,CENP-36,NSL1,NSL1","biotype":"protein_coding","ncbi_id":"284058","summary":"This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes. [provided by RefSeq, Jun 2012]","start":46041525,"end":46237041,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]"}, {"versioned_ensembl_gene_id":"ENSG00000278929.1","gene_symbol":"AP001784.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87565994,"end":87566421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248803.1","gene_symbol":"AC092349.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66622868,"end":66623177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254582.1","gene_symbol":"PSMA2P1","gene_name":"proteasome subunit alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43832]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130923","summary":null,"start":87329407,"end":87330052,"strand":-1,"description":"proteasome subunit alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43832]"}, {"versioned_ensembl_gene_id":"ENSG00000130175.9","gene_symbol":"PRKCSH","gene_name":"protein kinase C substrate 80K-H [Source:HGNC Symbol;Acc:HGNC:9411]","synonyms":"G19P1,VASAP-60,PLD1,PCLD,GIIB","biotype":"protein_coding","ncbi_id":"5589","summary":"This gene encodes the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in the endoplasmic reticulum. The encoded protein is an acidic phosphoprotein known to be a substrate for protein kinase C. Mutations in this gene have been associated with the autosomal dominant polycystic liver disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":11435288,"end":11450968,"strand":1,"description":"protein kinase C substrate 80K-H [Source:HGNC Symbol;Acc:HGNC:9411]"}, {"versioned_ensembl_gene_id":"ENSG00000228343.1","gene_symbol":"AC115618.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48579774,"end":48581157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268001.1","gene_symbol":"CARD8-AS1","gene_name":"CARD8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51408]","synonyms":"LOC100505812","biotype":"antisense_RNA","ncbi_id":"100505812","summary":null,"start":48255675,"end":48258199,"strand":1,"description":"CARD8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51408]"}, {"versioned_ensembl_gene_id":"ENSG00000204620.3","gene_symbol":"AC115618.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48568014,"end":48574860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254547.1","gene_symbol":"AC036111.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55867569,"end":55874537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227231.3","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30733457,"end":30734812,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000261194.1","gene_symbol":"LINC01898","gene_name":"long intergenic non-protein coding RNA 1898 [Source:HGNC Symbol;Acc:HGNC:52717]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505853","summary":null,"start":75696079,"end":75712385,"strand":-1,"description":"long intergenic non-protein coding RNA 1898 [Source:HGNC Symbol;Acc:HGNC:52717]"}, {"versioned_ensembl_gene_id":"ENSG00000182896.12","gene_symbol":"TMEM95","gene_name":"transmembrane protein 95 [Source:HGNC Symbol;Acc:HGNC:27898]","synonyms":"UNQ9390,MGC129793","biotype":"protein_coding","ncbi_id":"339168","summary":null,"start":7355123,"end":7357219,"strand":1,"description":"transmembrane protein 95 [Source:HGNC Symbol;Acc:HGNC:27898]"}, {"versioned_ensembl_gene_id":"ENSG00000237252.1","gene_symbol":"AC233981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76222637,"end":76223097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130812.10","gene_symbol":"ANGPTL6","gene_name":"angiopoietin like 6 [Source:HGNC Symbol;Acc:HGNC:23140]","synonyms":"ARP5,AGF","biotype":"protein_coding","ncbi_id":"83854","summary":null,"start":10092338,"end":10102796,"strand":-1,"description":"angiopoietin like 6 [Source:HGNC Symbol;Acc:HGNC:23140]"}, {"versioned_ensembl_gene_id":"ENSG00000127419.16","gene_symbol":"TMEM175","gene_name":"transmembrane protein 175 [Source:HGNC Symbol;Acc:HGNC:28709]","synonyms":"MGC4618","biotype":"protein_coding","ncbi_id":"84286","summary":null,"start":932387,"end":958656,"strand":1,"description":"transmembrane protein 175 [Source:HGNC Symbol;Acc:HGNC:28709]"}, {"versioned_ensembl_gene_id":"ENSG00000185100.10","gene_symbol":"ADSSL1","gene_name":"adenylosuccinate synthase like 1 [Source:HGNC Symbol;Acc:HGNC:20093]","synonyms":"FLJ38602","biotype":"protein_coding","ncbi_id":"122622","summary":"This gene encodes a member of the adenylosuccinate synthase family of proteins. The encoded muscle-specific enzyme plays a role in the purine nucleotide cycle by catalyzing the first step in the conversion of inosine monophosphate (IMP) to adenosine monophosphate (AMP). Mutations in this gene may cause adolescent onset distal myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":104724186,"end":104747325,"strand":1,"description":"adenylosuccinate synthase like 1 [Source:HGNC Symbol;Acc:HGNC:20093]"}, {"versioned_ensembl_gene_id":"ENSG00000070729.13","gene_symbol":"CNGB1","gene_name":"cyclic nucleotide gated channel beta 1 [Source:HGNC Symbol;Acc:HGNC:2151]","synonyms":"RP45,RCNCb,RCNC2,GARP,GAR1,CNGB1B,CNCG3L,CNCG2","biotype":"protein_coding","ncbi_id":"1258","summary":"In humans, the rod photoreceptor cGMP-gated cation channel helps regulate ion flow into the rod photoreceptor outer segment in response to light-induced alteration of the levels of intracellular cGMP. This channel consists of two subunits, alpha and beta, with the protein encoded by this gene representing the beta subunit. Defects in this gene are a cause of cause of retinitis pigmentosa type 45. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":57882340,"end":57971116,"strand":-1,"description":"cyclic nucleotide gated channel beta 1 [Source:HGNC Symbol;Acc:HGNC:2151]"}, {"versioned_ensembl_gene_id":"ENSG00000203985.10","gene_symbol":"LDLRAD1","gene_name":"low density lipoprotein receptor class A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32069]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388633","summary":null,"start":54007299,"end":54018186,"strand":-1,"description":"low density lipoprotein receptor class A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32069]"}, {"versioned_ensembl_gene_id":"ENSG00000231954.1","gene_symbol":"MTND2P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42123]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873228","summary":null,"start":130272479,"end":130273511,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42123]"}, {"versioned_ensembl_gene_id":"ENSG00000187821.8","gene_symbol":"HELT","gene_name":"helt bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:33783]","synonyms":"bHLHb44,Mgn,MEGANE,HESL,HCM1228","biotype":"protein_coding","ncbi_id":"391723","summary":null,"start":185018841,"end":185020804,"strand":1,"description":"helt bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:33783]"}, {"versioned_ensembl_gene_id":"ENSG00000229237.2","gene_symbol":"HMGN1P37","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728776","summary":null,"start":154817099,"end":154817401,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39421]"}, {"versioned_ensembl_gene_id":"ENSG00000237722.2","gene_symbol":"MTND1P29","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42078]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873216","summary":null,"start":130270440,"end":130272272,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42078]"}, {"versioned_ensembl_gene_id":"ENSG00000226192.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"hs6M1-4,OR6-5,dJ80I19.2,OR2J1P","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100958,"end":29101896,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000248616.1","gene_symbol":"AC109439.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136857628,"end":136858342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245849.6","gene_symbol":"RAD51-AS1","gene_name":"RAD51 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48621]","synonyms":"TODRA","biotype":"processed_transcript","ncbi_id":"100505648","summary":null,"start":40686724,"end":40695107,"strand":-1,"description":"RAD51 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48621]"}, {"versioned_ensembl_gene_id":"ENSG00000131462.7","gene_symbol":"TUBG1","gene_name":"tubulin gamma 1 [Source:HGNC Symbol;Acc:HGNC:12417]","synonyms":"TUBGCP1,TUBG","biotype":"protein_coding","ncbi_id":"7283","summary":"This gene encodes a member of the tubulin superfamily. The encoded protein localizes to the centrosome where it binds to microtubules as part of a complex referred to as the gamma-tubulin ring complex. The protein mediates microtubule nucleation and is required for microtubule formation and progression of the cell cycle. A pseudogene of this gene is found on chromosome 7. [provided by RefSeq, Jan 2009]","start":42609676,"end":42615234,"strand":1,"description":"tubulin gamma 1 [Source:HGNC Symbol;Acc:HGNC:12417]"}, {"versioned_ensembl_gene_id":"ENSG00000259178.1","gene_symbol":"AC023906.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52082302,"end":52086574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242327.1","gene_symbol":"AC023906.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52095295,"end":52095747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110442.11","gene_symbol":"COMMD9","gene_name":"COMM domain containing 9 [Source:HGNC Symbol;Acc:HGNC:25014]","synonyms":"HSPC166,FLJ31106","biotype":"protein_coding","ncbi_id":"29099","summary":null,"start":36269284,"end":36289449,"strand":-1,"description":"COMM domain containing 9 [Source:HGNC Symbol;Acc:HGNC:25014]"}, {"versioned_ensembl_gene_id":"ENSG00000250357.1","gene_symbol":"AC108935.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148693032,"end":148694323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197563.10","gene_symbol":"PIGN","gene_name":"phosphatidylinositol glycan anchor biosynthesis class N [Source:HGNC Symbol;Acc:HGNC:8967]","synonyms":"PIG-N,MDC4","biotype":"protein_coding","ncbi_id":"23556","summary":"This gene encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This protein is expressed in the endoplasmic reticulum and transfers phosphoethanolamine (EtNP) to the first mannose of the GPI anchor. Two alternatively spliced variants, which encode an identical isoform, have been reported. [provided by RefSeq, Jul 2008]","start":61905255,"end":62187118,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class N [Source:HGNC Symbol;Acc:HGNC:8967]"}, {"versioned_ensembl_gene_id":"ENSG00000114738.10","gene_symbol":"MAPKAPK3","gene_name":"mitogen-activated protein kinase-activated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:6888]","synonyms":"MAPKAP3,3pK","biotype":"protein_coding","ncbi_id":"7867","summary":"This gene encodes a member of the Ser/Thr protein kinase family. This kinase functions as a mitogen-activated protein kinase (MAP kinase)- activated protein kinase. MAP kinases are also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals. This kinase was shown to be activated by growth inducers and stress stimulation of cells. In vitro studies demonstrated that ERK, p38 MAP kinase and Jun N-terminal kinase were all able to phosphorylate and activate this kinase, which suggested the role of this kinase as an integrative element of signaling in both mitogen and stress responses. This kinase was reported to interact with, phosphorylate and repress the activity of E47, which is a basic helix-loop-helix transcription factor known to be involved in the regulation of tissue-specific gene expression and cell differentiation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011]","start":50611520,"end":50649297,"strand":1,"description":"mitogen-activated protein kinase-activated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:6888]"}, {"versioned_ensembl_gene_id":"ENSG00000235246.1","gene_symbol":"AL020993.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38231320,"end":38232248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253309.6","gene_symbol":"SERPINE3","gene_name":"serpin family E member 3 [Source:HGNC Symbol;Acc:HGNC:24774]","synonyms":null,"biotype":"protein_coding","ncbi_id":"647174","summary":null,"start":51335773,"end":51364735,"strand":1,"description":"serpin family E member 3 [Source:HGNC Symbol;Acc:HGNC:24774]"}, {"versioned_ensembl_gene_id":"ENSG00000229530.1","gene_symbol":"AL136097.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92339658,"end":92341663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204699.4","gene_symbol":"UBTFL3","gene_name":"upstream binding transcription factor, RNA polymerase I-like 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35402]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"129870","summary":null,"start":95625213,"end":95626236,"strand":1,"description":"upstream binding transcription factor, RNA polymerase I-like 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35402]"}, {"versioned_ensembl_gene_id":"ENSG00000280321.1","gene_symbol":"AC129502.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36196248,"end":36197901,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254615.2","gene_symbol":"AC027031.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106270144,"end":106272899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169495.4","gene_symbol":"HTRA4","gene_name":"HtrA serine peptidase 4 [Source:HGNC Symbol;Acc:HGNC:26909]","synonyms":"FLJ90724","biotype":"protein_coding","ncbi_id":"203100","summary":"This gene encodes a member of the HtrA family of proteases. The encoded protein contains a putative signal peptide, an insulin growth factor binding domain, a Kazal protease inhibitor domain, a conserved trypsin domain and a PDZ domain. Based on studies on other related family members, this enzyme may function as a secreted oligomeric chaperone protease to degrade misfolded secretory proteins. Other human HtrA proteins have been implicated in arthritis, tumor suppression, unfolded stress response, apoptosis, and aging. [provided by RefSeq, Oct 2008]","start":38974164,"end":38988662,"strand":1,"description":"HtrA serine peptidase 4 [Source:HGNC Symbol;Acc:HGNC:26909]"}, {"versioned_ensembl_gene_id":"ENSG00000274800.1","gene_symbol":"AC007204.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19978190,"end":19979610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146755.10","gene_symbol":"TRIM50","gene_name":"tripartite motif containing 50 [Source:HGNC Symbol;Acc:HGNC:19017]","synonyms":"TRIM50A,FLJ32804","biotype":"protein_coding","ncbi_id":"135892","summary":null,"start":73312539,"end":73328082,"strand":-1,"description":"tripartite motif containing 50 [Source:HGNC Symbol;Acc:HGNC:19017]"}, {"versioned_ensembl_gene_id":"ENSG00000248885.1","gene_symbol":"AC118465.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119126782,"end":119128444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183742.12","gene_symbol":"MACC1","gene_name":"MACC1, MET transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:30215]","synonyms":"SH3BP4L,7A5","biotype":"protein_coding","ncbi_id":"346389","summary":"MACC1 is a key regulator of the hepatocyte growth factor (HGF; MIM 142409)-HGF receptor (HGFR, or MET; MIM 164860) pathway, which is involved in cellular growth, epithelial-mesenchymal transition, angiogenesis, cell motility, invasiveness, and metastasis. Expression of MACC1 in colon cancer (MIM 114500) specimens is an independent prognostic indicator for metastasis formation and metastasis-free survival (Stein et al., 2009 [PubMed 19098908]).[supplied by OMIM, Mar 2009]","start":20134655,"end":20217404,"strand":-1,"description":"MACC1, MET transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:30215]"}, {"versioned_ensembl_gene_id":"ENSG00000167798.17","gene_symbol":"C3P1","gene_name":"complement component 3 precursor pseudogene [Source:HGNC Symbol;Acc:HGNC:34414]","synonyms":"CPLP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388503","summary":null,"start":10037803,"end":10074135,"strand":1,"description":"complement component 3 precursor pseudogene [Source:HGNC Symbol;Acc:HGNC:34414]"}, {"versioned_ensembl_gene_id":"ENSG00000253167.1","gene_symbol":"WASHC5-AS1","gene_name":"WASHC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43440]","synonyms":"KIAA0196-AS1","biotype":"antisense_RNA","ncbi_id":"106479020","summary":null,"start":125040684,"end":125044989,"strand":1,"description":"WASHC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43440]"}, {"versioned_ensembl_gene_id":"ENSG00000254431.1","gene_symbol":"AC084083.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125348196,"end":125351416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126368.5","gene_symbol":"NR1D1","gene_name":"nuclear receptor subfamily 1 group D member 1 [Source:HGNC Symbol;Acc:HGNC:7962]","synonyms":"THRAL,THRA1,Rev-ErbAalpha,hRev,ear-1","biotype":"protein_coding","ncbi_id":"9572","summary":"This gene encodes a transcription factor that is a member of the nuclear receptor subfamily 1. The encoded protein is a ligand-sensitive transcription factor that negatively regulates the expression of core clock proteins. In particular this protein represses the circadian clock transcription factor aryl hydrocarbon receptor nuclear translocator-like protein 1 (ARNTL). This protein may also be involved in regulating genes that function in metabolic, inflammatory and cardiovascular processes. [provided by RefSeq, Jan 2013]","start":40092787,"end":40100725,"strand":-1,"description":"nuclear receptor subfamily 1 group D member 1 [Source:HGNC Symbol;Acc:HGNC:7962]"}, {"versioned_ensembl_gene_id":"ENSG00000269534.5","gene_symbol":"AC011466.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48118432,"end":48127706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217631.1","gene_symbol":"FO393413.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49273600,"end":49273794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244653.1","gene_symbol":"UBFD1P1","gene_name":"ubiquitin family domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42389]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130484","summary":null,"start":98434034,"end":98434847,"strand":1,"description":"ubiquitin family domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42389]"}, {"versioned_ensembl_gene_id":"ENSG00000184924.5","gene_symbol":"PTRHD1","gene_name":"peptidyl-tRNA hydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33782]","synonyms":"LOC391356,C2orf79","biotype":"protein_coding","ncbi_id":"391356","summary":"This gene encodes the enzyme peptidyl-tRNA hydrolase. Peptidyl-tRNA hydrolases perform the essential function of recycling peptidyl-tRNAs. Mutations in this gene are associated with autosomal-recessive intellectual disability and parkinsonism. [provided by RefSeq, May 2017]","start":24789734,"end":24793382,"strand":-1,"description":"peptidyl-tRNA hydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33782]"}, {"versioned_ensembl_gene_id":"ENSG00000274290.2","gene_symbol":"HIST1H2BE","gene_name":"histone cluster 1 H2B family member e [Source:HGNC Symbol;Acc:HGNC:4753]","synonyms":"H2BFH,H2B/h,H2B.h","biotype":"protein_coding","ncbi_id":"8344","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. The protein has antibacterial and antifungal antimicrobial activity. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26172059,"end":26184655,"strand":1,"description":"histone cluster 1 H2B family member e [Source:HGNC Symbol;Acc:HGNC:4753]"}, {"versioned_ensembl_gene_id":"ENSG00000144724.19","gene_symbol":"PTPRG","gene_name":"protein tyrosine phosphatase, receptor type G [Source:HGNC Symbol;Acc:HGNC:9671]","synonyms":"RPTPG,PTPG","biotype":"protein_coding","ncbi_id":"5793","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this PTP contains a carbonic anhydrase-like (CAH) domain, which is also found in the extracellular region of PTPRBETA/ZETA. This gene is located in a chromosomal region that is frequently deleted in renal cell carcinoma and lung carcinoma, thus is thought to be a candidate tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":61561569,"end":62297613,"strand":1,"description":"protein tyrosine phosphatase, receptor type G [Source:HGNC Symbol;Acc:HGNC:9671]"}, {"versioned_ensembl_gene_id":"ENSG00000253118.1","gene_symbol":"AC022695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92351912,"end":92352148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271590.1","gene_symbol":"AC108463.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111210995,"end":111212476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263041.1","gene_symbol":"AL513324.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117825903,"end":117830518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261777.5","gene_symbol":"AC012184.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":70315640,"end":70346747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215148.8","gene_symbol":"PRSS41","gene_name":"protease, serine 41 [Source:HGNC Symbol;Acc:HGNC:30715]","synonyms":"TESSP1","biotype":"protein_coding","ncbi_id":"360226","summary":null,"start":2798485,"end":2805302,"strand":1,"description":"protease, serine 41 [Source:HGNC Symbol;Acc:HGNC:30715]"}, {"versioned_ensembl_gene_id":"ENSG00000233277.1","gene_symbol":"LINC01728","gene_name":"long intergenic non-protein coding RNA 1728 [Source:HGNC Symbol;Acc:HGNC:52516]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372626","summary":null,"start":43894720,"end":43895468,"strand":1,"description":"long intergenic non-protein coding RNA 1728 [Source:HGNC Symbol;Acc:HGNC:52516]"}, {"versioned_ensembl_gene_id":"ENSG00000150045.11","gene_symbol":"KLRF1","gene_name":"killer cell lectin like receptor F1 [Source:HGNC Symbol;Acc:HGNC:13342]","synonyms":"CLEC5C,NKp80","biotype":"protein_coding","ncbi_id":"51348","summary":"KLRF1, an activating homodimeric C-type lectin-like receptor (CTLR), is expressed on nearly all natural killer (NK) cells and stimulates their cytoxicity and cytokine release (Kuttruff et al., 2009 [PubMed 18922855]).[supplied by OMIM, Oct 2009]","start":9827481,"end":9845007,"strand":1,"description":"killer cell lectin like receptor F1 [Source:HGNC Symbol;Acc:HGNC:13342]"}, {"versioned_ensembl_gene_id":"ENSG00000280719.1","gene_symbol":"PCAT5","gene_name":"prostate cancer associated transcript 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48665]","synonyms":"TPCAT-10-36067,LINC01452","biotype":"lincRNA","ncbi_id":"102578074","summary":null,"start":35778302,"end":35800920,"strand":1,"description":"prostate cancer associated transcript 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48665]"}, {"versioned_ensembl_gene_id":"ENSG00000273176.1","gene_symbol":"AL008635.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35298838,"end":35299541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259430.1","gene_symbol":"CERS3-AS1","gene_name":"CERS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51431]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723320","summary":null,"start":100372939,"end":100437914,"strand":1,"description":"CERS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51431]"}, {"versioned_ensembl_gene_id":"ENSG00000253382.3","gene_symbol":"POU5F1P2","gene_name":"POU class 5 homeobox 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33309]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129512","summary":null,"start":102621509,"end":102622331,"strand":-1,"description":"POU class 5 homeobox 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33309]"}, {"versioned_ensembl_gene_id":"ENSG00000198417.6","gene_symbol":"MT1F","gene_name":"metallothionein 1F [Source:HGNC Symbol;Acc:HGNC:7398]","synonyms":"MT1","biotype":"protein_coding","ncbi_id":"4494","summary":null,"start":56657694,"end":56660698,"strand":1,"description":"metallothionein 1F [Source:HGNC Symbol;Acc:HGNC:7398]"}, {"versioned_ensembl_gene_id":"ENSG00000211599.2","gene_symbol":"IGKV5-2","gene_name":"immunoglobulin kappa variable 5-2 [Source:HGNC Symbol;Acc:HGNC:5835]","synonyms":"IGKV52,B2","biotype":"IG_V_gene","ncbi_id":"28907","summary":null,"start":88897232,"end":88897784,"strand":1,"description":"immunoglobulin kappa variable 5-2 [Source:HGNC Symbol;Acc:HGNC:5835]"}, {"versioned_ensembl_gene_id":"ENSG00000168938.5","gene_symbol":"PPIC","gene_name":"peptidylprolyl isomerase C [Source:HGNC Symbol;Acc:HGNC:9256]","synonyms":"CYPC","biotype":"protein_coding","ncbi_id":"5480","summary":"The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase)) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. Similar to other PPIases, this protein can bind immunosuppressant cyclosporin A. [provided by RefSeq, Jul 2008]","start":123023250,"end":123036741,"strand":-1,"description":"peptidylprolyl isomerase C [Source:HGNC Symbol;Acc:HGNC:9256]"}, {"versioned_ensembl_gene_id":"ENSG00000228629.2","gene_symbol":"AC092295.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36528318,"end":36535235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198930.12","gene_symbol":"CSAG1","gene_name":"chondrosarcoma associated gene 1 [Source:HGNC Symbol;Acc:HGNC:24294]","synonyms":"CT24.1,CSAGE","biotype":"protein_coding","ncbi_id":"158511","summary":"This gene encodes a member of a family of tumor antigens. The protein is expressed in chondrosarcomas, but may also be expressed in normal tissues such as testis. Alternative splicing of this gene results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":152727484,"end":152733735,"strand":-1,"description":"chondrosarcoma associated gene 1 [Source:HGNC Symbol;Acc:HGNC:24294]"}, {"versioned_ensembl_gene_id":"ENSG00000247675.6","gene_symbol":"LRP4-AS1","gene_name":"LRP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44128]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507401","summary":null,"start":46846412,"end":46874396,"strand":1,"description":"LRP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44128]"}, {"versioned_ensembl_gene_id":"ENSG00000258498.8","gene_symbol":"DIO3OS","gene_name":"DIO3 opposite strand/antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:20348]","synonyms":"NCRNA00041,DIO3-AS1,C14orf134","biotype":"lincRNA","ncbi_id":"64150","summary":"The mouse and human DIO3OS and DIO3 (MIM 601038) genes overlap and are transcribed in opposite directions. The mouse Dio3 gene is imprinted from the paternal allele during fetal development, suggesting that DIO3OS is a noncoding gene that may have a role in maintaining monoallelic expression of DIO3 (Hernandez et al., 2004 [PubMed 14962667]).[supplied by OMIM, Mar 2008]","start":101552221,"end":101560431,"strand":-1,"description":"DIO3 opposite strand/antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:20348]"}, {"versioned_ensembl_gene_id":"ENSG00000143436.10","gene_symbol":"MRPL9","gene_name":"mitochondrial ribosomal protein L9 [Source:HGNC Symbol;Acc:HGNC:14277]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65005","summary":"This is a nuclear gene encoding a protein component of the 39S subunit of the mitochondrial ribosome. Alternative splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 8. [provided by RefSeq, Jul 2014]","start":151759643,"end":151763564,"strand":-1,"description":"mitochondrial ribosomal protein L9 [Source:HGNC Symbol;Acc:HGNC:14277]"}, {"versioned_ensembl_gene_id":"ENSG00000225950.8","gene_symbol":"NTF4","gene_name":"neurotrophin 4 [Source:HGNC Symbol;Acc:HGNC:8024]","synonyms":"NTF5,NT-4/5,GLC1O","biotype":"protein_coding","ncbi_id":"4909","summary":"This gene is a member of a family of neurotrophic factors, neurotrophins, that control survival and differentiation of mammalian neurons. The expression of this gene is ubiquitous and less influenced by environmental signals. While knock-outs of other neurotrophins including nerve growth factor, brain-derived neurotrophic factor, and neurotrophin 3 prove lethal during early postnatal development, NTF5-deficient mice only show minor cellular deficits and develop normally to adulthood. [provided by RefSeq, Jul 2008]","start":49061066,"end":49065054,"strand":-1,"description":"neurotrophin 4 [Source:HGNC Symbol;Acc:HGNC:8024]"}, {"versioned_ensembl_gene_id":"ENSG00000211592.8","gene_symbol":"IGKC","gene_name":"immunoglobulin kappa constant [Source:HGNC Symbol;Acc:HGNC:5716]","synonyms":"HCAK1","biotype":"IG_C_gene","ncbi_id":"3514","summary":null,"start":88857161,"end":88857683,"strand":-1,"description":"immunoglobulin kappa constant [Source:HGNC Symbol;Acc:HGNC:5716]"}, {"versioned_ensembl_gene_id":"ENSG00000248424.1","gene_symbol":"OR51K1P","gene_name":"olfactory receptor family 51 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15202]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"81278","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5430653,"end":5431602,"strand":-1,"description":"olfactory receptor family 51 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15202]"}, {"versioned_ensembl_gene_id":"ENSG00000258588.3","gene_symbol":"TRIM6-TRIM34","gene_name":"TRIM6-TRIM34 readthrough [Source:HGNC Symbol;Acc:HGNC:33440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"445372","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This gene represents a readthrough transcript from genes TRIM6 and TRIM34, and it was described as a splice variant of TRIM34. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. [provided by RefSeq, Nov 2009]","start":5596725,"end":5644398,"strand":1,"description":"TRIM6-TRIM34 readthrough [Source:HGNC Symbol;Acc:HGNC:33440]"}, {"versioned_ensembl_gene_id":"ENSG00000246100.3","gene_symbol":"LINC00900","gene_name":"long intergenic non-protein coding RNA 900 [Source:HGNC Symbol;Acc:HGNC:27444]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283143","summary":null,"start":115754248,"end":115760627,"strand":-1,"description":"long intergenic non-protein coding RNA 900 [Source:HGNC Symbol;Acc:HGNC:27444]"}, {"versioned_ensembl_gene_id":"ENSG00000214761.3","gene_symbol":"HNRNPA1P15","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39133]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421353","summary":null,"start":125595669,"end":125596628,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39133]"}, {"versioned_ensembl_gene_id":"ENSG00000225535.6","gene_symbol":"LINC01393","gene_name":"long intergenic non-protein coding RNA 1393 [Source:HGNC Symbol;Acc:HGNC:50669]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724386","summary":null,"start":115078958,"end":115126314,"strand":1,"description":"long intergenic non-protein coding RNA 1393 [Source:HGNC Symbol;Acc:HGNC:50669]"}, {"versioned_ensembl_gene_id":"ENSG00000169260.11","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994770,"end":29005301,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000280296.1","gene_symbol":"AL137058.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52497097,"end":52500195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271237.1","gene_symbol":"HMGB1P50","gene_name":"high mobility group box 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:52368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729125","summary":null,"start":49551308,"end":49552652,"strand":1,"description":"high mobility group box 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:52368]"}, {"versioned_ensembl_gene_id":"ENSG00000081307.12","gene_symbol":"UBA5","gene_name":"ubiquitin like modifier activating enzyme 5 [Source:HGNC Symbol;Acc:HGNC:23230]","synonyms":"UBE1DC1,FLJ23251","biotype":"protein_coding","ncbi_id":"79876","summary":"This gene encodes a member of the E1-like ubiquitin-activating enzyme family. This protein activates ubiquitin-fold modifier 1, a ubiquitin-like post-translational modifier protein, via the formation of a high-energy thioester bond. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been identified on chromosome 1. [provided by RefSeq, Feb 2016]","start":132654446,"end":132678097,"strand":1,"description":"ubiquitin like modifier activating enzyme 5 [Source:HGNC Symbol;Acc:HGNC:23230]"}, {"versioned_ensembl_gene_id":"ENSG00000274810.4","gene_symbol":"NPHP3-ACAD11","gene_name":"NPHP3-ACAD11 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48351]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532724","summary":"This locus represents naturally occurring read-through transcription between the neighboring NPHP3 (nephronophthisis 3, adolescent) and ACAD11 (acyl-CoA dehydrogenase family, member 11) genes on chromosome 3. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":132558142,"end":132722459,"strand":-1,"description":"NPHP3-ACAD11 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48351]"}, {"versioned_ensembl_gene_id":"ENSG00000186795.1","gene_symbol":"KCNK18","gene_name":"potassium two pore domain channel subfamily K member 18 [Source:HGNC Symbol;Acc:HGNC:19439]","synonyms":"TRIK,TRESK2,TRESK-2,TRESK,K2p18.1","biotype":"protein_coding","ncbi_id":"338567","summary":"Potassium channels play a role in many cellular processes including maintenance of the action potential, muscle contraction, hormone secretion, osmotic regulation, and ion flow. This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains and the encoded protein functions as an outward rectifying potassium channel. A mutation in this gene has been found to be associated with migraine with aura.[provided by RefSeq, Jan 2011]","start":117197489,"end":117210299,"strand":1,"description":"potassium two pore domain channel subfamily K member 18 [Source:HGNC Symbol;Acc:HGNC:19439]"}, {"versioned_ensembl_gene_id":"ENSG00000267363.1","gene_symbol":"AC092296.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36379351,"end":36380912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142065.13","gene_symbol":"ZFP14","gene_name":"ZFP14 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:29312]","synonyms":"ZNF531,KIAA1559","biotype":"protein_coding","ncbi_id":"57677","summary":null,"start":36334453,"end":36379199,"strand":-1,"description":"ZFP14 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:29312]"}, {"versioned_ensembl_gene_id":"ENSG00000255580.1","gene_symbol":"AP000462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115363629,"end":115377931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237103.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31571039,"end":31575129,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000270423.1","gene_symbol":"AP001981.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109985243,"end":109985660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258017.1","gene_symbol":"AC011603.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49127782,"end":49147869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263786.1","gene_symbol":"AC022211.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75145261,"end":75146546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261666.1","gene_symbol":"LINC00560","gene_name":"long intergenic non-protein coding RNA 560 [Source:HGNC Symbol;Acc:HGNC:43704]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861553","summary":null,"start":88626853,"end":88630397,"strand":1,"description":"long intergenic non-protein coding RNA 560 [Source:HGNC Symbol;Acc:HGNC:43704]"}, {"versioned_ensembl_gene_id":"ENSG00000257808.1","gene_symbol":"AC073573.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53159586,"end":53161000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175216.14","gene_symbol":"CKAP5","gene_name":"cytoskeleton associated protein 5 [Source:HGNC Symbol;Acc:HGNC:28959]","synonyms":"TOGp,TOG,KIAA0097,ch-TOG","biotype":"protein_coding","ncbi_id":"9793","summary":"This gene encodes a cytoskeleton-associated protein which belongs to the TOG/XMAP215 family. The N-terminal half of this protein contains a microtubule-binding domain and the C-terminal half contains a KXGS motif for binding tubulin dimers. This protein has two distinct roles in spindle formation; it protects kinetochore microtubules from depolymerization and plays an essential role in centrosomal microtubule assembly. This protein may be necessary for the proper interaction of microtubules with the cell cortex for directional cell movement. It also plays a role in translation of the myelin basic protein (MBP) mRNA by interacting with heterogeneous nuclear ribonucleoprotein (hnRNP) A2, which associates with MBP. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":46743048,"end":46846308,"strand":-1,"description":"cytoskeleton associated protein 5 [Source:HGNC Symbol;Acc:HGNC:28959]"}, {"versioned_ensembl_gene_id":"ENSG00000066468.22","gene_symbol":"FGFR2","gene_name":"fibroblast growth factor receptor 2 [Source:HGNC Symbol;Acc:HGNC:3689]","synonyms":"CFD1,CEK3,CD332,TK25,BEK,TK14,KGFR,K-SAM,JWS,ECT1","biotype":"protein_coding","ncbi_id":"2263","summary":"The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis. Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]","start":121478334,"end":121598458,"strand":-1,"description":"fibroblast growth factor receptor 2 [Source:HGNC Symbol;Acc:HGNC:3689]"}, {"versioned_ensembl_gene_id":"ENSG00000223940.1","gene_symbol":"KRT8P8","gene_name":"keratin 8 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402429","summary":null,"start":152479577,"end":152481024,"strand":1,"description":"keratin 8 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33362]"}, {"versioned_ensembl_gene_id":"ENSG00000223967.1","gene_symbol":"AL603910.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73526744,"end":73526879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239557.1","gene_symbol":"AC092045.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52373652,"end":52374882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253327.2","gene_symbol":"RAD21-AS1","gene_name":"RAD21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32158]","synonyms":"NCRNA00255,C8orf81","biotype":"antisense_RNA","ncbi_id":"644660","summary":null,"start":116874424,"end":116876868,"strand":1,"description":"RAD21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32158]"}, {"versioned_ensembl_gene_id":"ENSG00000119638.12","gene_symbol":"NEK9","gene_name":"NIMA related kinase 9 [Source:HGNC Symbol;Acc:HGNC:18591]","synonyms":"NERCC,Nek8,MGC16714,DKFZp434D0935","biotype":"protein_coding","ncbi_id":"91754","summary":"This gene encodes a member of the NimA (never in mitosis A) family of serine/threonine protein kinases. The encoded protein is activated in mitosis and, in turn, activates other family members during mitosis. This protein also mediates cellular processes that are essential for interphase progression. [provided by RefSeq, Jul 2016]","start":75079353,"end":75127344,"strand":-1,"description":"NIMA related kinase 9 [Source:HGNC Symbol;Acc:HGNC:18591]"}, {"versioned_ensembl_gene_id":"ENSG00000204437.7","gene_symbol":"CTSLP6","gene_name":"cathepsin L pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23611]","synonyms":"CTSLL6,CTSL1P6,bA479O17.1","biotype":"unprocessed_pseudogene","ncbi_id":"642413","summary":null,"start":79870375,"end":79873903,"strand":-1,"description":"cathepsin L pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23611]"}, {"versioned_ensembl_gene_id":"ENSG00000155926.13","gene_symbol":"SLA","gene_name":"Src like adaptor [Source:HGNC Symbol;Acc:HGNC:10902]","synonyms":"SLAP-1,SLAP,SLA1,hSLAP","biotype":"protein_coding","ncbi_id":"6503","summary":null,"start":133036724,"end":133103054,"strand":-1,"description":"Src like adaptor [Source:HGNC Symbol;Acc:HGNC:10902]"}, {"versioned_ensembl_gene_id":"ENSG00000254744.3","gene_symbol":"AC084855.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99970215,"end":99974010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177034.14","gene_symbol":"MTX3","gene_name":"metaxin 3 [Source:HGNC Symbol;Acc:HGNC:24812]","synonyms":null,"biotype":"protein_coding","ncbi_id":"345778","summary":null,"start":79976731,"end":79991262,"strand":-1,"description":"metaxin 3 [Source:HGNC Symbol;Acc:HGNC:24812]"}, {"versioned_ensembl_gene_id":"ENSG00000112893.9","gene_symbol":"MAN2A1","gene_name":"mannosidase alpha class 2A member 1 [Source:HGNC Symbol;Acc:HGNC:6824]","synonyms":"GOLIM7,MANA2","biotype":"protein_coding","ncbi_id":"4124","summary":"This gene encodes a glycosyl hydrolase that localizes to the Golgi and catalyzes the final hydrolytic step in the asparagine-linked oligosaccharide (N-glycan) maturation pathway. Mutations in the mouse homolog of this gene have been shown to cause a systemic autoimmune disease similar to human systemic lupus erythematosus. [provided by RefSeq, Dec 2013]","start":109689366,"end":109869625,"strand":1,"description":"mannosidase alpha class 2A member 1 [Source:HGNC Symbol;Acc:HGNC:6824]"}, {"versioned_ensembl_gene_id":"ENSG00000241562.2","gene_symbol":"RPL7P5","gene_name":"ribosomal protein L7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:28886]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654381","summary":null,"start":99551382,"end":99552117,"strand":-1,"description":"ribosomal protein L7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:28886]"}, {"versioned_ensembl_gene_id":"ENSG00000064199.6","gene_symbol":"SPA17","gene_name":"sperm autoantigenic protein 17 [Source:HGNC Symbol;Acc:HGNC:11210]","synonyms":"SP17,CT22","biotype":"protein_coding","ncbi_id":"53340","summary":"This gene encodes a protein present at the cell surface. The N-terminus has sequence similarity to human cAMP-dependent protein kinase A (PKA) type II alpha regulatory subunit (RIIa) while the C-terminus has an IQ calmodulin-binding motif. The central portion of the protein has carbohydrate binding motifs and likely functions in cell-cell adhesion. The protein was initially characterized by its involvement in the binding of sperm to the zona pellucida of the oocyte. Recent studies indicate that it is also involved in additional cell-cell adhesion functions such as immune cell migration and metastasis. A retrotransposed pseudogene is present on chromosome 10q22.[provided by RefSeq, Jan 2009]","start":124673798,"end":124697518,"strand":1,"description":"sperm autoantigenic protein 17 [Source:HGNC Symbol;Acc:HGNC:11210]"}, {"versioned_ensembl_gene_id":"ENSG00000229443.1","gene_symbol":"LINC00433","gene_name":"long intergenic non-protein coding RNA 433 [Source:HGNC Symbol;Acc:HGNC:42768]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874168","summary":null,"start":88540864,"end":88545509,"strand":1,"description":"long intergenic non-protein coding RNA 433 [Source:HGNC Symbol;Acc:HGNC:42768]"}, {"versioned_ensembl_gene_id":"ENSG00000224082.1","gene_symbol":"UBTFL8","gene_name":"upstream binding transcription factor, RNA polymerase I-like 8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44476]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643182","summary":null,"start":5080212,"end":5084429,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44476]"}, {"versioned_ensembl_gene_id":"ENSG00000258455.1","gene_symbol":"AL158801.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55325834,"end":55339501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225289.1","gene_symbol":"RPL29P29","gene_name":"ribosomal protein L29 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36577]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271474","summary":null,"start":88236547,"end":88236969,"strand":-1,"description":"ribosomal protein L29 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36577]"}, {"versioned_ensembl_gene_id":"ENSG00000257480.1","gene_symbol":"MRPL2P1","gene_name":"mitochondrial ribosomal protein L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29698]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347894","summary":null,"start":89752913,"end":89753831,"strand":1,"description":"mitochondrial ribosomal protein L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29698]"}, {"versioned_ensembl_gene_id":"ENSG00000230017.6","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29724084,"end":29746526,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000239686.1","gene_symbol":"AL158801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55282296,"end":55282643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248440.1","gene_symbol":"AC091917.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109497877,"end":109499108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248876.1","gene_symbol":"AC091917.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109470843,"end":109471586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230801.1","gene_symbol":"AL160175.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31808503,"end":31808749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167635.11","gene_symbol":"ZNF146","gene_name":"zinc finger protein 146 [Source:HGNC Symbol;Acc:HGNC:12931]","synonyms":"OZF","biotype":"protein_coding","ncbi_id":"7705","summary":null,"start":36214602,"end":36238774,"strand":1,"description":"zinc finger protein 146 [Source:HGNC Symbol;Acc:HGNC:12931]"}, {"versioned_ensembl_gene_id":"ENSG00000120533.12","gene_symbol":"ENY2","gene_name":"ENY2, transcription and export complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:24449]","synonyms":"Sus1,FLJ20480,DC6","biotype":"protein_coding","ncbi_id":"56943","summary":null,"start":109334324,"end":109345953,"strand":1,"description":"ENY2, transcription and export complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:24449]"}, {"versioned_ensembl_gene_id":"ENSG00000275825.1","gene_symbol":"AC139494.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69814552,"end":69814989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228046.2","gene_symbol":"MTCO3P40","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52143]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075188","summary":null,"start":82427350,"end":82428025,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52143]"}, {"versioned_ensembl_gene_id":"ENSG00000183458.13","gene_symbol":"AC138932.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14911551,"end":14935708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240890.2","gene_symbol":"AC020633.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132386522,"end":132389074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104960.15","gene_symbol":"PTOV1","gene_name":"prostate tumor overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:9632]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53635","summary":"This gene encodes a protein that was found to be overexpressed in prostate adenocarcinomas. The encoded protein was found to interact with the lipid raft protein flotillin-1 and shuttle it from the cytoplasm to the nucleus in a cell cycle dependent manner. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":49850735,"end":49860744,"strand":1,"description":"prostate tumor overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:9632]"}, {"versioned_ensembl_gene_id":"ENSG00000276122.1","gene_symbol":"AC026336.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130138693,"end":130140768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012048.20","gene_symbol":"BRCA1","gene_name":"BRCA1, DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1100]","synonyms":"PPP1R53,FANCS,BRCC1,RNF53","biotype":"protein_coding","ncbi_id":"672","summary":"This gene encodes a 190 kD nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The BRCA1 gene contains 22 exons spanning about 110 kb of DNA. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2020]","start":43044295,"end":43170245,"strand":-1,"description":"BRCA1, DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1100]"}, {"versioned_ensembl_gene_id":"ENSG00000229528.1","gene_symbol":"AC119677.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40863914,"end":40876670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198879.11","gene_symbol":"SFMBT2","gene_name":"Scm-like with four mbt domains 2 [Source:HGNC Symbol;Acc:HGNC:20256]","synonyms":"KIAA1617","biotype":"protein_coding","ncbi_id":"57713","summary":null,"start":7158624,"end":7411486,"strand":-1,"description":"Scm-like with four mbt domains 2 [Source:HGNC Symbol;Acc:HGNC:20256]"}, {"versioned_ensembl_gene_id":"ENSG00000143374.16","gene_symbol":"TARS2","gene_name":"threonyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:30740]","synonyms":"TARSL1,FLJ12528","biotype":"protein_coding","ncbi_id":"80222","summary":"This gene encodes a member of the class-II aminoacyl-tRNA synthetase family. The encoded protein is a mitochondrial aminoacyl-tRNA synthetase. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 4. [provided by RefSeq, Dec 2012]","start":150487364,"end":150507609,"strand":1,"description":"threonyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:30740]"}, {"versioned_ensembl_gene_id":"ENSG00000259154.1","gene_symbol":"DUX4L17","gene_name":"double homeobox 4 like 17 [Source:HGNC Symbol;Acc:HGNC:37717]","synonyms":"DUXY3","biotype":"unprocessed_pseudogene","ncbi_id":"643001","summary":null,"start":11314921,"end":11316187,"strand":1,"description":"double homeobox 4 like 17 [Source:HGNC Symbol;Acc:HGNC:37717]"}, {"versioned_ensembl_gene_id":"ENSG00000236651.1","gene_symbol":"DLX2-AS1","gene_name":"DLX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50638]","synonyms":"TCONS_00003049","biotype":"lincRNA","ncbi_id":"104326193","summary":null,"start":172103006,"end":172109982,"strand":1,"description":"DLX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50638]"}, {"versioned_ensembl_gene_id":"ENSG00000234707.2","gene_symbol":"AC074351.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54759425,"end":54804928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254482.1","gene_symbol":"AP003102.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109637468,"end":109638128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256357.1","gene_symbol":"AL132708.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94430633,"end":94464730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273247.5","gene_symbol":"AC097376.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139411927,"end":139454034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212659.1","gene_symbol":"KRTAP9-6","gene_name":"keratin associated protein 9-6 [Source:HGNC Symbol;Acc:HGNC:18914]","synonyms":"KRTAP9L2,KAP9.6","biotype":"protein_coding","ncbi_id":"100507608","summary":null,"start":41265339,"end":41266641,"strand":1,"description":"keratin associated protein 9-6 [Source:HGNC Symbol;Acc:HGNC:18914]"}, {"versioned_ensembl_gene_id":"ENSG00000241595.2","gene_symbol":"KRTAP9-4","gene_name":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]","synonyms":"KAP9.4","biotype":"protein_coding","ncbi_id":"85280","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41249687,"end":41250653,"strand":1,"description":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]"}, {"versioned_ensembl_gene_id":"ENSG00000185742.6","gene_symbol":"C11orf87","gene_name":"chromosome 11 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:33788]","synonyms":"NEURIM1,LOH11CR1A,LOC399947","biotype":"protein_coding","ncbi_id":"399947","summary":null,"start":109422120,"end":109429114,"strand":1,"description":"chromosome 11 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:33788]"}, {"versioned_ensembl_gene_id":"ENSG00000278212.1","gene_symbol":"AC134878.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11153858,"end":11159013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234692.1","gene_symbol":"AL355601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115252538,"end":115254251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169194.9","gene_symbol":"IL13","gene_name":"interleukin 13 [Source:HGNC Symbol;Acc:HGNC:5973]","synonyms":"BHR1,ALRH,P600,MGC116789,MGC116788,MGC116786,IL-13","biotype":"protein_coding","ncbi_id":"3596","summary":"This gene encodes an immunoregulatory cytokine produced primarily by activated Th2 cells. This cytokine is involved in several stages of B-cell maturation and differentiation. It up-regulates CD23 and MHC class II expression, and promotes IgE isotype switching of B cells. This cytokine down-regulates macrophage activity, thereby inhibits the production of pro-inflammatory cytokines and chemokines. This cytokine is found to be critical to the pathogenesis of allergen-induced asthma but operates through mechanisms independent of IgE and eosinophils. This gene, IL3, IL5, IL4, and CSF2 form a cytokine gene cluster on chromosome 5q, with this gene particularly close to IL4. [provided by RefSeq, Jul 2008]","start":132656263,"end":132661110,"strand":1,"description":"interleukin 13 [Source:HGNC Symbol;Acc:HGNC:5973]"}, {"versioned_ensembl_gene_id":"ENSG00000183955.12","gene_symbol":"KMT5A","gene_name":"lysine methyltransferase 5A [Source:HGNC Symbol;Acc:HGNC:29489]","synonyms":"SETD8,SET8,SET07,PR-Set7","biotype":"protein_coding","ncbi_id":"387893","summary":"The protein encoded by this gene is a protein-lysine N-methyltransferase that can monomethylate Lys-20 of histone H4 to effect transcriptional repression of some genes. The encoded protein is required for cell proliferation and plays a role in chromatin condensation. [provided by RefSeq, May 2016]","start":123383773,"end":123409358,"strand":1,"description":"lysine methyltransferase 5A [Source:HGNC Symbol;Acc:HGNC:29489]"}, {"versioned_ensembl_gene_id":"ENSG00000274480.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724486,"end":54736514,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000159184.7","gene_symbol":"HOXB13","gene_name":"homeobox B13 [Source:HGNC Symbol;Acc:HGNC:5112]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10481","summary":"This gene encodes a transcription factor that belongs to the homeobox gene family. Genes of this family are highly conserved among vertebrates and essential for vertebrate embryonic development. This gene has been implicated to play a role in fetal skin development and cutaneous regeneration. In mice, a similar gene was shown to exhibit temporal and spatial colinearity in the main body axis of the embryo, but was not expressed in the secondary axes, which suggests functions in body patterning along the axis. This gene and other HOXB genes form a gene cluster at chromosome the 17q21-22 region. [provided by RefSeq, Jul 2008]","start":48724763,"end":48729178,"strand":-1,"description":"homeobox B13 [Source:HGNC Symbol;Acc:HGNC:5112]"}, {"versioned_ensembl_gene_id":"ENSG00000232938.2","gene_symbol":"RPL23AP87","gene_name":"ribosomal protein L23a pseudogene 87 [Source:HGNC Symbol;Acc:HGNC:51578]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"388574","summary":null,"start":83226897,"end":83240804,"strand":1,"description":"ribosomal protein L23a pseudogene 87 [Source:HGNC Symbol;Acc:HGNC:51578]"}, {"versioned_ensembl_gene_id":"ENSG00000197536.11","gene_symbol":"C5orf56","gene_name":"chromosome 5 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:33838]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441108","summary":null,"start":132410636,"end":132488702,"strand":1,"description":"chromosome 5 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:33838]"}, {"versioned_ensembl_gene_id":"ENSG00000279143.1","gene_symbol":"AC139099.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":83132647,"end":83136150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227413.1","gene_symbol":"AL022238.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40433136,"end":40433641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157445.14","gene_symbol":"CACNA2D3","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 3 [Source:HGNC Symbol;Acc:HGNC:15460]","synonyms":"HSA272268","biotype":"protein_coding","ncbi_id":"55799","summary":"This gene encodes a member of the alpha-2/delta subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Various versions of each of these subunits exist, either expressed from similar genes or the result of alternative splicing. Research on a highly similar protein in rabbit suggests the protein described in this record is cleaved into alpha-2 and delta subunits. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":54122547,"end":55074557,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit alpha2delta 3 [Source:HGNC Symbol;Acc:HGNC:15460]"}, {"versioned_ensembl_gene_id":"ENSG00000251552.1","gene_symbol":"COQ10BP2","gene_name":"coenzyme Q10B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421072","summary":null,"start":83279921,"end":83280644,"strand":-1,"description":"coenzyme Q10B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44913]"}, {"versioned_ensembl_gene_id":"ENSG00000279340.1","gene_symbol":"AC090617.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2122342,"end":2122508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255167.1","gene_symbol":"AC090857.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21260061,"end":21262570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271309.1","gene_symbol":"AC140113.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11107389,"end":11107596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196156.4","gene_symbol":"KRTAP4-3","gene_name":"keratin associated protein 4-3 [Source:HGNC Symbol;Acc:HGNC:18908]","synonyms":"KAP4.3","biotype":"protein_coding","ncbi_id":"85290","summary":null,"start":41167231,"end":41168194,"strand":-1,"description":"keratin associated protein 4-3 [Source:HGNC Symbol;Acc:HGNC:18908]"}, {"versioned_ensembl_gene_id":"ENSG00000271365.1","gene_symbol":"AC140113.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11107065,"end":11107263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239705.1","gene_symbol":"AL354710.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125241663,"end":125257018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152433.14","gene_symbol":"ZNF547","gene_name":"zinc finger protein 547 [Source:HGNC Symbol;Acc:HGNC:26432]","synonyms":"FLJ31100","biotype":"protein_coding","ncbi_id":"284306","summary":null,"start":57363477,"end":57379565,"strand":1,"description":"zinc finger protein 547 [Source:HGNC Symbol;Acc:HGNC:26432]"}, {"versioned_ensembl_gene_id":"ENSG00000125826.20","gene_symbol":"RBCK1","gene_name":"RANBP2-type and C3HC4-type zinc finger containing 1 [Source:HGNC Symbol;Acc:HGNC:15864]","synonyms":"ZRANB4,XAP4,UBCE7IP3,RNF54,RBCK2,HOIL1,C20orf18","biotype":"protein_coding","ncbi_id":"10616","summary":"The protein encoded by this gene is similar to mouse UIP28/UbcM4 interacting protein. Alternative splicing has been observed at this locus, resulting in distinct isoforms. [provided by RefSeq, Jul 2008]","start":407498,"end":430966,"strand":1,"description":"RANBP2-type and C3HC4-type zinc finger containing 1 [Source:HGNC Symbol;Acc:HGNC:15864]"}, {"versioned_ensembl_gene_id":"ENSG00000236770.1","gene_symbol":"AC079325.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":74549399,"end":74552737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225632.1","gene_symbol":"AL161644.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54285405,"end":54287371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275638.1","gene_symbol":"AC011939.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65655620,"end":65656085,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106266.10","gene_symbol":"SNX8","gene_name":"sorting nexin 8 [Source:HGNC Symbol;Acc:HGNC:14972]","synonyms":"Mvp1","biotype":"protein_coding","ncbi_id":"29886","summary":null,"start":2251770,"end":2354318,"strand":-1,"description":"sorting nexin 8 [Source:HGNC Symbol;Acc:HGNC:14972]"}, {"versioned_ensembl_gene_id":"ENSG00000243406.6","gene_symbol":"MRPS31P5","gene_name":"mitochondrial ribosomal protein S31 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39253]","synonyms":"MRPS31P3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100887750","summary":null,"start":52167709,"end":52194465,"strand":-1,"description":"mitochondrial ribosomal protein S31 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39253]"}, {"versioned_ensembl_gene_id":"ENSG00000231737.7","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"FB19,PNUTS,CAT53,p99","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30645036,"end":30663248,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000080845.17","gene_symbol":"DLGAP4","gene_name":"DLG associated protein 4 [Source:HGNC Symbol;Acc:HGNC:24476]","synonyms":"SAPAP4,KIAA0964,DAP4","biotype":"protein_coding","ncbi_id":"22839","summary":"The product of this gene is a membrane-associated guanylate kinase found at the postsynaptic density in neuronal cells. It is a signaling molecule that can interact with potassium channels and receptors, as well as other signaling molecules. The protein encoded by this gene can interact with PSD-95 through its guanylate kinase domain and may be involved in clustering PSD-95 in the postsynaptic density region. The encoded protein is one of at least four similar proteins that have been found. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":36306336,"end":36528637,"strand":1,"description":"DLG associated protein 4 [Source:HGNC Symbol;Acc:HGNC:24476]"}, {"versioned_ensembl_gene_id":"ENSG00000170234.12","gene_symbol":"PWWP2A","gene_name":"PWWP domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29406]","synonyms":"KIAA1935","biotype":"protein_coding","ncbi_id":"114825","summary":null,"start":160061801,"end":160119423,"strand":-1,"description":"PWWP domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29406]"}, {"versioned_ensembl_gene_id":"ENSG00000235372.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30024180,"end":30025470,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000178202.12","gene_symbol":"KDELC2","gene_name":"KDEL motif containing 2 [Source:HGNC Symbol;Acc:HGNC:28496]","synonyms":"MGC33424","biotype":"protein_coding","ncbi_id":"143888","summary":null,"start":108472105,"end":108498432,"strand":-1,"description":"KDEL motif containing 2 [Source:HGNC Symbol;Acc:HGNC:28496]"}, {"versioned_ensembl_gene_id":"ENSG00000166261.10","gene_symbol":"ZNF202","gene_name":"zinc finger protein 202 [Source:HGNC Symbol;Acc:HGNC:12994]","synonyms":"ZSCAN42,ZKSCAN10","biotype":"protein_coding","ncbi_id":"7753","summary":null,"start":123724177,"end":123741675,"strand":-1,"description":"zinc finger protein 202 [Source:HGNC Symbol;Acc:HGNC:12994]"}, {"versioned_ensembl_gene_id":"ENSG00000152413.14","gene_symbol":"HOMER1","gene_name":"homer scaffolding protein 1 [Source:HGNC Symbol;Acc:HGNC:17512]","synonyms":"Ves-1,SYN47,HOMER-1B","biotype":"protein_coding","ncbi_id":"9456","summary":"This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. [provided by RefSeq, Jul 2008]","start":79372636,"end":79514217,"strand":-1,"description":"homer scaffolding protein 1 [Source:HGNC Symbol;Acc:HGNC:17512]"}, {"versioned_ensembl_gene_id":"ENSG00000213755.3","gene_symbol":"AC093270.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79510434,"end":79510919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227045.1","gene_symbol":"AL589765.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151701026,"end":151708386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250906.1","gene_symbol":"AC131953.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40812779,"end":40826151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264272.1","gene_symbol":"AC100786.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74256896,"end":74262020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165949.12","gene_symbol":"IFI27","gene_name":"interferon alpha inducible protein 27 [Source:HGNC Symbol;Acc:HGNC:5397]","synonyms":"P27,ISG12,FAM14D","biotype":"protein_coding","ncbi_id":"3429","summary":null,"start":94104836,"end":94116698,"strand":1,"description":"interferon alpha inducible protein 27 [Source:HGNC Symbol;Acc:HGNC:5397]"}, {"versioned_ensembl_gene_id":"ENSG00000176978.13","gene_symbol":"DPP7","gene_name":"dipeptidyl peptidase 7 [Source:HGNC Symbol;Acc:HGNC:14892]","synonyms":"DPPII,DPP2","biotype":"protein_coding","ncbi_id":"29952","summary":"The protein encoded by this gene is a post-proline cleaving aminopeptidase expressed in quiescent lymphocytes. The resting lymphocytes are maintained through suppression of apoptosis, a state which is disrupted by inhibition of this novel serine protease. The enzyme has strong sequence homology with prolylcarboxypeptidase and is active at both acidic and neutral pH. [provided by RefSeq, Jul 2008]","start":137110542,"end":137115177,"strand":-1,"description":"dipeptidyl peptidase 7 [Source:HGNC Symbol;Acc:HGNC:14892]"}, {"versioned_ensembl_gene_id":"ENSG00000234667.2","gene_symbol":"ACTBP13","gene_name":"actin, beta pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44626]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"389120","summary":null,"start":49873347,"end":49877305,"strand":-1,"description":"actin, beta pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44626]"}, {"versioned_ensembl_gene_id":"ENSG00000090097.21","gene_symbol":"PCBP4","gene_name":"poly(rC) binding protein 4 [Source:HGNC Symbol;Acc:HGNC:8652]","synonyms":"MCG10,LIP4","biotype":"protein_coding","ncbi_id":"57060","summary":"This gene encodes a member of the KH-domain protein subfamily. Proteins of this subfamily, also referred to as alpha-CPs, bind to RNA with a specificity for C-rich pyrimidine regions. Alpha-CPs play important roles in post-transcriptional activities and have different cellular distributions. This gene is induced by the p53 tumor suppressor, and the encoded protein can suppress cell proliferation by inducing apoptosis and cell cycle arrest in G(2)-M. This gene's protein is found in the cytoplasm, yet it lacks the nuclear localization signals found in other subfamily members. Multiple alternatively spliced transcript variants have been described, but the full-length nature for only some has been determined. [provided by RefSeq, Jul 2008]","start":51957454,"end":51974016,"strand":-1,"description":"poly(rC) binding protein 4 [Source:HGNC Symbol;Acc:HGNC:8652]"}, {"versioned_ensembl_gene_id":"ENSG00000257586.1","gene_symbol":"AC018448.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38994803,"end":38996882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236208.1","gene_symbol":"C10orf71-AS1","gene_name":"C10orf71 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45007]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506769","summary":null,"start":49296112,"end":49299018,"strand":-1,"description":"C10orf71 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45007]"}, {"versioned_ensembl_gene_id":"ENSG00000070404.9","gene_symbol":"FSTL3","gene_name":"follistatin like 3 [Source:HGNC Symbol;Acc:HGNC:3973]","synonyms":"FSRP,FLRG","biotype":"protein_coding","ncbi_id":"10272","summary":"Follistatin-like 3 is a secreted glycoprotein of the follistatin-module-protein family. It may have a role in leukemogenesis. [provided by RefSeq, Jul 2008]","start":676365,"end":683399,"strand":1,"description":"follistatin like 3 [Source:HGNC Symbol;Acc:HGNC:3973]"}, {"versioned_ensembl_gene_id":"ENSG00000254387.1","gene_symbol":"MYL12AP1","gene_name":"myosin light chain 12A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"157667","summary":null,"start":93849561,"end":93850075,"strand":1,"description":"myosin light chain 12A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51648]"}, {"versioned_ensembl_gene_id":"ENSG00000264750.1","gene_symbol":"AC032019.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73641026,"end":73643106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224120.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30725496,"end":30731566,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000205847.6","gene_symbol":"OR7E91P","gene_name":"olfactory receptor family 7 subfamily E member 91 pseudogene [Source:HGNC Symbol;Acc:HGNC:14747]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79315","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":71024127,"end":71029893,"strand":1,"description":"olfactory receptor family 7 subfamily E member 91 pseudogene [Source:HGNC Symbol;Acc:HGNC:14747]"}, {"versioned_ensembl_gene_id":"ENSG00000278035.1","gene_symbol":"AL121895.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36233851,"end":36234297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267666.2","gene_symbol":"AC004156.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":663482,"end":669500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265010.1","gene_symbol":"AC087301.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73243093,"end":73244706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206285.6","gene_symbol":"B3GALT4","gene_name":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]","synonyms":"GalT4,beta3Gal-T4","biotype":"protein_coding","ncbi_id":"8705","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is oriented telomere to centromere in close proximity to the ribosomal protein S18 gene. The functionality of the encoded protein is limited to ganglioseries glycolipid biosynthesis. [provided by RefSeq, Jul 2008]","start":33205959,"end":33207652,"strand":1,"description":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]"}, {"versioned_ensembl_gene_id":"ENSG00000272559.1","gene_symbol":"AC103710.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4736178,"end":4737078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255982.1","gene_symbol":"NXPE2P1","gene_name":"neurexophilin and PC-esterase domain family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44082]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101926945","summary":null,"start":114512706,"end":114513431,"strand":-1,"description":"neurexophilin and PC-esterase domain family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44082]"}, {"versioned_ensembl_gene_id":"ENSG00000256533.1","gene_symbol":"AP002373.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114453064,"end":114454123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283599.2","gene_symbol":"BX276092.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71667542,"end":71671524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230934.1","gene_symbol":"BX276092.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71691932,"end":71692179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213757.3","gene_symbol":"AC020898.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79284132,"end":79284918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138785.14","gene_symbol":"INTS12","gene_name":"integrator complex subunit 12 [Source:HGNC Symbol;Acc:HGNC:25067]","synonyms":"SBBI22,PHF22,INT12","biotype":"protein_coding","ncbi_id":"57117","summary":"INTS12 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":105682627,"end":105895986,"strand":-1,"description":"integrator complex subunit 12 [Source:HGNC Symbol;Acc:HGNC:25067]"}, {"versioned_ensembl_gene_id":"ENSG00000233476.3","gene_symbol":"EEF1A1P6","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3201]","synonyms":"EEF1AL4","biotype":"processed_pseudogene","ncbi_id":"221838","summary":null,"start":22510616,"end":22511999,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:3201]"}, {"versioned_ensembl_gene_id":"ENSG00000100373.9","gene_symbol":"UPK3A","gene_name":"uroplakin 3A [Source:HGNC Symbol;Acc:HGNC:12580]","synonyms":"UPK3","biotype":"protein_coding","ncbi_id":"7380","summary":"This gene encodes a member of the uroplakin family, a group of transmembrane proteins that form complexes on the apical surface of the bladder epithelium. Mutations in this gene may be associated with renal adysplasia. Alternatively spliced transcript variants have been described.[provided by RefSeq, Nov 2009]","start":45284982,"end":45295874,"strand":1,"description":"uroplakin 3A [Source:HGNC Symbol;Acc:HGNC:12580]"}, {"versioned_ensembl_gene_id":"ENSG00000229069.2","gene_symbol":"BX248093.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29182359,"end":29183294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229195.1","gene_symbol":"AC009495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165794857,"end":165846091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235192.1","gene_symbol":"AC009495.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165794851,"end":165810010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227036.6","gene_symbol":"LINC00511","gene_name":"long intergenic non-protein coding RNA 511 [Source:HGNC Symbol;Acc:HGNC:43564]","synonyms":"onco-lncRNA-12","biotype":"lincRNA","ncbi_id":"400619","summary":null,"start":72323123,"end":72640472,"strand":-1,"description":"long intergenic non-protein coding RNA 511 [Source:HGNC Symbol;Acc:HGNC:43564]"}, {"versioned_ensembl_gene_id":"ENSG00000259528.1","gene_symbol":"AC068397.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73255334,"end":73256109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230163.1","gene_symbol":"AL122010.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34850694,"end":34851555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255811.1","gene_symbol":"AL121988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34761426,"end":34788097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249857.1","gene_symbol":"AC027338.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82940458,"end":82940983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189433.5","gene_symbol":"GJB4","gene_name":"gap junction protein beta 4 [Source:HGNC Symbol;Acc:HGNC:4286]","synonyms":"CX30.3","biotype":"protein_coding","ncbi_id":"127534","summary":"This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment. [provided by RefSeq, Dec 2009]","start":34759741,"end":34763724,"strand":1,"description":"gap junction protein beta 4 [Source:HGNC Symbol;Acc:HGNC:4286]"}, {"versioned_ensembl_gene_id":"ENSG00000041982.15","gene_symbol":"TNC","gene_name":"tenascin C [Source:HGNC Symbol;Acc:HGNC:5318]","synonyms":"DFNA56,TN,MGC167029,HXB","biotype":"protein_coding","ncbi_id":"3371","summary":"This gene encodes an extracellular matrix protein with a spatially and temporally restricted tissue distribution. This protein is homohexameric with disulfide-linked subunits, and contains multiple EGF-like and fibronectin type-III domains. It is implicated in guidance of migrating neurons as well as axons during development, synaptic plasticity, and neuronal regeneration. [provided by RefSeq, Jul 2011]","start":115019578,"end":115118257,"strand":-1,"description":"tenascin C [Source:HGNC Symbol;Acc:HGNC:5318]"}, {"versioned_ensembl_gene_id":"ENSG00000267109.1","gene_symbol":"AC011990.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70312831,"end":70368916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135272.10","gene_symbol":"MDFIC","gene_name":"MyoD family inhibitor domain containing [Source:HGNC Symbol;Acc:HGNC:28870]","synonyms":"MDFIC1,HIC","biotype":"protein_coding","ncbi_id":"29969","summary":"This gene product is a member of a family of proteins characterized by a specific cysteine-rich C-terminal domain, which is involved in transcriptional regulation of viral genome expression. Alternative translation initiation from an upstream non-AUG (GUG), and an in-frame, downstream AUG codon, results in the production of two isoforms, p40 and p32, respectively, which have different subcellular localization; p32 is mainly found in the cytoplasm, whereas p40 is targeted to the nucleolus. Both isoforms have transcriptional regulatory activity that is attributable to the cysteine-rich C-terminal domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":114922154,"end":115019202,"strand":1,"description":"MyoD family inhibitor domain containing [Source:HGNC Symbol;Acc:HGNC:28870]"}, {"versioned_ensembl_gene_id":"ENSG00000230258.6","gene_symbol":"AC005208.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70017324,"end":70128859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280422.1","gene_symbol":"AC115284.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51951849,"end":51953902,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113811.10","gene_symbol":"SELENOK","gene_name":"selenoprotein K [Source:HGNC Symbol;Acc:HGNC:30394]","synonyms":"SELK","biotype":"protein_coding","ncbi_id":"58515","summary":"The protein encoded by this gene belongs to the selenoprotein K family. It is a transmembrane protein that is localized in the endoplasmic reticulum (ER), and is involved in ER-associated degradation (ERAD) of misfolded, glycosylated proteins. It also has a role in the protection of cells from ER stress-induced apoptosis. Knockout studies in mice show the importance of this gene in promoting Ca(2+) flux in immune cells and mounting effective immune response. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Pseudogenes of this locus have been identified on chromosomes 6 and 19.[provided by RefSeq, Aug 2017]","start":53884410,"end":53891988,"strand":-1,"description":"selenoprotein K [Source:HGNC Symbol;Acc:HGNC:30394]"}, {"versioned_ensembl_gene_id":"ENSG00000243224.1","gene_symbol":"AC006252.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52239258,"end":52241097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107021.15","gene_symbol":"TBC1D13","gene_name":"TBC1 domain family member 13 [Source:HGNC Symbol;Acc:HGNC:25571]","synonyms":"FLJ10743","biotype":"protein_coding","ncbi_id":"54662","summary":null,"start":128787204,"end":128810432,"strand":1,"description":"TBC1 domain family member 13 [Source:HGNC Symbol;Acc:HGNC:25571]"}, {"versioned_ensembl_gene_id":"ENSG00000154263.17","gene_symbol":"ABCA10","gene_name":"ATP binding cassette subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:30]","synonyms":"EST698739","biotype":"protein_coding","ncbi_id":"10349","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. [provided by RefSeq, Jul 2008]","start":69147214,"end":69244846,"strand":-1,"description":"ATP binding cassette subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:30]"}, {"versioned_ensembl_gene_id":"ENSG00000273082.1","gene_symbol":"Z73429.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33922422,"end":33922766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227344.2","gene_symbol":"HAUS6P1","gene_name":"HAUS augmin like complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43764]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653175","summary":null,"start":53187388,"end":53188938,"strand":1,"description":"HAUS augmin like complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43764]"}, {"versioned_ensembl_gene_id":"ENSG00000187753.12","gene_symbol":"C9orf153","gene_name":"chromosome 9 open reading frame 153 [Source:HGNC Symbol;Acc:HGNC:31456]","synonyms":"bA507D14.1","biotype":"protein_coding","ncbi_id":"389766","summary":null,"start":86220265,"end":86259657,"strand":-1,"description":"chromosome 9 open reading frame 153 [Source:HGNC Symbol;Acc:HGNC:31456]"}, {"versioned_ensembl_gene_id":"ENSG00000250522.1","gene_symbol":"AC004066.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105540190,"end":105552355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081052.11","gene_symbol":"COL4A4","gene_name":"collagen type IV alpha 4 chain [Source:HGNC Symbol;Acc:HGNC:2206]","synonyms":"CA44","biotype":"protein_coding","ncbi_id":"1286","summary":"This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. This particular collagen IV subunit, however, is only found in a subset of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease). Two transcripts, differing only in their transcription start sites, have been identified for this gene and, as is common for collagen genes, multiple polyadenylation sites are found in the 3' UTR. [provided by RefSeq, Jul 2008]","start":227002711,"end":227164113,"strand":-1,"description":"collagen type IV alpha 4 chain [Source:HGNC Symbol;Acc:HGNC:2206]"}, {"versioned_ensembl_gene_id":"ENSG00000230423.1","gene_symbol":"AL731684.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170735751,"end":170736545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234950.1","gene_symbol":"RBMY2OP","gene_name":"RNA binding motif protein, Y-linked, family 2, member O pseudogene [Source:HGNC Symbol;Acc:HGNC:23894]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379005","summary":null,"start":9951553,"end":9959423,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member O pseudogene [Source:HGNC Symbol;Acc:HGNC:23894]"}, {"versioned_ensembl_gene_id":"ENSG00000225532.1","gene_symbol":"AL731684.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170736173,"end":170737777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284196.1","gene_symbol":"AL158064.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":80041725,"end":80074557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280177.1","gene_symbol":"AC004408.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":39165073,"end":39167849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225484.6","gene_symbol":"NUTM2B-AS1","gene_name":"NUTM2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51204]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101060691","summary":null,"start":79663088,"end":79826594,"strand":-1,"description":"NUTM2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51204]"}, {"versioned_ensembl_gene_id":"ENSG00000250567.1","gene_symbol":"AC010406.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103408941,"end":103412511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117597.17","gene_symbol":"DIEXF","gene_name":"digestive organ expansion factor homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:28440]","synonyms":"C1orf107,UTP25,MGC29875,DEF","biotype":"protein_coding","ncbi_id":"27042","summary":null,"start":209828007,"end":209857565,"strand":1,"description":"digestive organ expansion factor homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:28440]"}, {"versioned_ensembl_gene_id":"ENSG00000231583.1","gene_symbol":"AC108938.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110500100,"end":110500235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082293.12","gene_symbol":"COL19A1","gene_name":"collagen type XIX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2196]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1310","summary":"This gene encodes the alpha chain of type XIX collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Although the function of this collagen is not known, other members of this collagen family are found in association with fibril-forming collagens such as type I and II, and serve to maintain the integrity of the extracellular matrix. The transcript produced from this gene has an unusually large 3' UTR which has not been completely sequenced. [provided by RefSeq, Jul 2008]","start":69866571,"end":70209976,"strand":1,"description":"collagen type XIX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2196]"}, {"versioned_ensembl_gene_id":"ENSG00000230371.1","gene_symbol":"KARSP2","gene_name":"lysyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39208]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419560","summary":null,"start":113130416,"end":113132054,"strand":1,"description":"lysyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39208]"}, {"versioned_ensembl_gene_id":"ENSG00000134640.2","gene_symbol":"MTNR1B","gene_name":"melatonin receptor 1B [Source:HGNC Symbol;Acc:HGNC:7464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4544","summary":"This gene encodes one of two high affinity forms of a receptor for melatonin, the primary hormone secreted by the pineal gland. This gene product is an integral membrane protein that is a G-protein coupled, 7-transmembrane receptor. It is found primarily in the retina and brain although this detection requires RT-PCR. It is thought to participate in light-dependent functions in the retina and may be involved in the neurobiological effects of melatonin. [provided by RefSeq, Jul 2008]","start":92969720,"end":92985066,"strand":1,"description":"melatonin receptor 1B [Source:HGNC Symbol;Acc:HGNC:7464]"}, {"versioned_ensembl_gene_id":"ENSG00000256092.2","gene_symbol":"AC137767.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123363868,"end":123366113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227080.2","gene_symbol":"AC012441.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51388430,"end":51389114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227233.1","gene_symbol":"CICP17","gene_name":"capicua transcriptional repressor pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:48827]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642663","summary":null,"start":51382284,"end":51384660,"strand":1,"description":"capicua transcriptional repressor pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:48827]"}, {"versioned_ensembl_gene_id":"ENSG00000101203.16","gene_symbol":"COL20A1","gene_name":"collagen type XX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:14670]","synonyms":"KIAA1510","biotype":"protein_coding","ncbi_id":"57642","summary":null,"start":63293186,"end":63334851,"strand":1,"description":"collagen type XX alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:14670]"}, {"versioned_ensembl_gene_id":"ENSG00000277156.1","gene_symbol":"AL589743.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19267115,"end":19268164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111796.3","gene_symbol":"KLRB1","gene_name":"killer cell lectin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6373]","synonyms":"CD161,NKR-P1A,NKR-P1,NKR,hNKR-P1A,CLEC5B","biotype":"protein_coding","ncbi_id":"3820","summary":"Natural killer (NK) cells are lymphocytes that mediate cytotoxicity and secrete cytokines after immune stimulation. Several genes of the C-type lectin superfamily, including the rodent NKRP1 family of glycoproteins, are expressed by NK cells and may be involved in the regulation of NK cell function. The KLRB1 protein contains an extracellular domain with several motifs characteristic of C-type lectins, a transmembrane domain, and a cytoplasmic domain. The KLRB1 protein is classified as a type II membrane protein because it has an external C terminus. [provided by RefSeq, Jul 2008]","start":9594551,"end":9607886,"strand":-1,"description":"killer cell lectin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6373]"}, {"versioned_ensembl_gene_id":"ENSG00000123411.14","gene_symbol":"IKZF4","gene_name":"IKAROS family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:13179]","synonyms":"ZNFN1A4,Eos","biotype":"protein_coding","ncbi_id":"64375","summary":"Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Eos, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002]","start":56007659,"end":56038435,"strand":1,"description":"IKAROS family zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:13179]"}, {"versioned_ensembl_gene_id":"ENSG00000218475.2","gene_symbol":"ACTG1P18","gene_name":"actin gamma 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418924","summary":null,"start":101430411,"end":101431553,"strand":-1,"description":"actin gamma 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51498]"}, {"versioned_ensembl_gene_id":"ENSG00000134057.14","gene_symbol":"CCNB1","gene_name":"cyclin B1 [Source:HGNC Symbol;Acc:HGNC:1579]","synonyms":"CCNB","biotype":"protein_coding","ncbi_id":"891","summary":"The protein encoded by this gene is a regulatory protein involved in mitosis. The gene product complexes with p34(cdc2) to form the maturation-promoting factor (MPF). The encoded protein is necessary for proper control of the G2/M transition phase of the cell cycle. [provided by RefSeq, Aug 2017]","start":69167010,"end":69178245,"strand":1,"description":"cyclin B1 [Source:HGNC Symbol;Acc:HGNC:1579]"}, {"versioned_ensembl_gene_id":"ENSG00000255287.1","gene_symbol":"SNRPGP16","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480270","summary":null,"start":92937441,"end":92937666,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49373]"}, {"versioned_ensembl_gene_id":"ENSG00000231140.3","gene_symbol":"BX005214.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39395737,"end":39397406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227532.1","gene_symbol":"AC002542.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117187548,"end":117187740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228368.1","gene_symbol":"AC106873.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116965846,"end":116967472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224429.7","gene_symbol":"LINC00539","gene_name":"long intergenic non-protein coding RNA 539 [Source:HGNC Symbol;Acc:HGNC:43672]","synonyms":"LINC00422","biotype":"lincRNA","ncbi_id":"100652865","summary":null,"start":21303515,"end":21348721,"strand":-1,"description":"long intergenic non-protein coding RNA 539 [Source:HGNC Symbol;Acc:HGNC:43672]"}, {"versioned_ensembl_gene_id":"ENSG00000011083.8","gene_symbol":"SLC6A7","gene_name":"solute carrier family 6 member 7 [Source:HGNC Symbol;Acc:HGNC:11054]","synonyms":"PROT","biotype":"protein_coding","ncbi_id":"6534","summary":"This gene is a member of the gamma-aminobutyric acid (GABA) neurotransmitter gene family and encodes a high-affinity mammalian brain L-proline transporter protein. This transporter protein differs from other sodium-dependent plasma membrane carriers by its pharmacological specificity, kinetic properties, and ionic requirements. [provided by RefSeq, Jul 2008]","start":150189957,"end":150222788,"strand":1,"description":"solute carrier family 6 member 7 [Source:HGNC Symbol;Acc:HGNC:11054]"}, {"versioned_ensembl_gene_id":"ENSG00000175213.2","gene_symbol":"ZNF408","gene_name":"zinc finger protein 408 [Source:HGNC Symbol;Acc:HGNC:20041]","synonyms":"FLJ12827","biotype":"protein_coding","ncbi_id":"79797","summary":"The protein encoded by this gene contains ten tandem zinc fingers and an N-terminal SET domain, so it is likely a DNA binding protein that interacts with other proteins. In adults, the encoded protein is expressed most highly in retina. Consequently, defects in this gene have been associated with familial exudative vitreoretinopathy (FEVR) and retinitis pigmentosa (RP). [provided by RefSeq, Dec 2016]","start":46700818,"end":46705912,"strand":1,"description":"zinc finger protein 408 [Source:HGNC Symbol;Acc:HGNC:20041]"}, {"versioned_ensembl_gene_id":"ENSG00000147381.11","gene_symbol":"MAGEA4","gene_name":"MAGE family member A4 [Source:HGNC Symbol;Acc:HGNC:6802]","synonyms":"MGC21336,MAGE4B,MAGE4A,MAGE4,MAGE-X2,MAGE-41,CT1.4","biotype":"protein_coding","ncbi_id":"4103","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Several variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2020]","start":151912509,"end":151925170,"strand":1,"description":"MAGE family member A4 [Source:HGNC Symbol;Acc:HGNC:6802]"}, {"versioned_ensembl_gene_id":"ENSG00000198538.10","gene_symbol":"ZNF28","gene_name":"zinc finger protein 28 [Source:HGNC Symbol;Acc:HGNC:13073]","synonyms":"KOX24,DKFZp781D0275","biotype":"protein_coding","ncbi_id":"7576","summary":null,"start":52797409,"end":52857600,"strand":-1,"description":"zinc finger protein 28 [Source:HGNC Symbol;Acc:HGNC:13073]"}, {"versioned_ensembl_gene_id":"ENSG00000213711.3","gene_symbol":"PHBP7","gene_name":"prohibitin pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39286]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"548599","summary":null,"start":85898903,"end":85899716,"strand":1,"description":"prohibitin pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39286]"}, {"versioned_ensembl_gene_id":"ENSG00000182674.5","gene_symbol":"KCNB2","gene_name":"potassium voltage-gated channel subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:6232]","synonyms":"Kv2.2","biotype":"protein_coding","ncbi_id":"9312","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel. The gene is expressed in gastrointestinal smooth muscle cells. [provided by RefSeq, Jul 2008]","start":72537391,"end":72938349,"strand":1,"description":"potassium voltage-gated channel subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:6232]"}, {"versioned_ensembl_gene_id":"ENSG00000268282.1","gene_symbol":"AC010328.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53004040,"end":53005150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212710.4","gene_symbol":"CTAGE1","gene_name":"cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:24346]","synonyms":"cTAGE-1,CTAGE,CT21.2,CT21.1,cTAGE-2","biotype":"protein_coding","ncbi_id":"64693","summary":null,"start":22413601,"end":22417915,"strand":-1,"description":"cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:24346]"}, {"versioned_ensembl_gene_id":"ENSG00000154723.12","gene_symbol":"ATP5J","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6 [Source:HGNC Symbol;Acc:HGNC:847]","synonyms":"ATP5,CF6,ATPM,ATP5A","biotype":"protein_coding","ncbi_id":"522","summary":"Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo complex has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the F6 subunit of the Fo complex. The F6 subunit is required for F1 and Fo interactions. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has 1 or more pseudogenes. [provided by RefSeq, Feb 2016]","start":25716503,"end":25735673,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6 [Source:HGNC Symbol;Acc:HGNC:847]"}, {"versioned_ensembl_gene_id":"ENSG00000255808.1","gene_symbol":"AP003065.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72643237,"end":72659407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277356.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769746,"end":54783981,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000257501.6","gene_symbol":"AC007424.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":97713412,"end":97761859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257157.1","gene_symbol":"AC018659.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97679879,"end":97680047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237628.2","gene_symbol":"MTCO2P19","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075223","summary":null,"start":102797531,"end":102798128,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52035]"}, {"versioned_ensembl_gene_id":"ENSG00000256673.1","gene_symbol":"AC141557.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9398355,"end":9414851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231722.1","gene_symbol":"AC012075.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81418723,"end":81419302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280124.1","gene_symbol":"AP003485.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91184934,"end":91185543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237759.1","gene_symbol":"AL590483.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":244107365,"end":244109011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262533.1","gene_symbol":"AC090617.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2042900,"end":2043425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229006.7","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RNF76,RFP","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28903869,"end":28924846,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000112655.15","gene_symbol":"PTK7","gene_name":"protein tyrosine kinase 7 (inactive) [Source:HGNC Symbol;Acc:HGNC:9618]","synonyms":"CCK4","biotype":"protein_coding","ncbi_id":"5754","summary":"This gene encodes a member of the receptor protein tyrosine kinase family of proteins that transduce extracellular signals across the cell membrane. The encoded protein lacks detectable catalytic tyrosine kinase activity, is involved in the Wnt signaling pathway and plays a role in multiple cellular processes including polarity and adhesion. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":43076268,"end":43161719,"strand":1,"description":"protein tyrosine kinase 7 (inactive) [Source:HGNC Symbol;Acc:HGNC:9618]"}, {"versioned_ensembl_gene_id":"ENSG00000137409.19","gene_symbol":"MTCH1","gene_name":"mitochondrial carrier 1 [Source:HGNC Symbol;Acc:HGNC:17586]","synonyms":"SLC25A49,PSAP,CGI-64","biotype":"protein_coding","ncbi_id":"23787","summary":"This gene encodes a member of the mitochondrial carrier family. The encoded protein is localized to the mitochondrion inner membrane and induces apoptosis independent of the proapoptotic proteins Bax and Bak. Pseudogenes on chromosomes 6 and 11 have been identified for this gene. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Oct 2012]","start":36968141,"end":36986298,"strand":-1,"description":"mitochondrial carrier 1 [Source:HGNC Symbol;Acc:HGNC:17586]"}, {"versioned_ensembl_gene_id":"ENSG00000267395.5","gene_symbol":"DM1-AS","gene_name":"DM1 locus antisense RNA [Source:HGNC Symbol;Acc:HGNC:53125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"109729182","summary":null,"start":45767796,"end":45772504,"strand":1,"description":"DM1 locus antisense RNA [Source:HGNC Symbol;Acc:HGNC:53125]"}, {"versioned_ensembl_gene_id":"ENSG00000232536.1","gene_symbol":"AL365436.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":151540516,"end":151561855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113721.13","gene_symbol":"PDGFRB","gene_name":"platelet derived growth factor receptor beta [Source:HGNC Symbol;Acc:HGNC:8804]","synonyms":"PDGFR1,PDGFR,JTK12,CD140b","biotype":"protein_coding","ncbi_id":"5159","summary":"The protein encoded by this gene is a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer (PDGFB or PDGFD) or a heterodimer (PDGFA and PDGFB). This gene is essential for normal development of the cardiovascular system and aids in rearrangement of the actin cytoskeleton. This gene is flanked on chromosome 5 by the genes for granulocyte-macrophage colony-stimulating factor and macrophage-colony stimulating factor receptor; all three genes may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12, that fuses this gene to that of the ETV6 gene, results in chronic myeloproliferative disorder with eosinophilia. [provided by RefSeq, Aug 2017]","start":150113837,"end":150155872,"strand":-1,"description":"platelet derived growth factor receptor beta [Source:HGNC Symbol;Acc:HGNC:8804]"}, {"versioned_ensembl_gene_id":"ENSG00000260176.1","gene_symbol":"AC141586.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2644084,"end":2645214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279573.1","gene_symbol":"AC134407.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67955314,"end":67957291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241577.1","gene_symbol":"AC060234.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":48883955,"end":48935213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233665.8","gene_symbol":"AC060234.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48976554,"end":48993046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255051.1","gene_symbol":"BCAS2P1","gene_name":"BCAS2, pre-mRNA processing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39594]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127960","summary":null,"start":83132056,"end":83134737,"strand":1,"description":"BCAS2, pre-mRNA processing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39594]"}, {"versioned_ensembl_gene_id":"ENSG00000074370.17","gene_symbol":"ATP2A3","gene_name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:813]","synonyms":"SERCA3","biotype":"protein_coding","ncbi_id":"489","summary":"This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in calcium sequestration associated with muscular excitation and contraction. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":3923870,"end":3964464,"strand":-1,"description":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3 [Source:HGNC Symbol;Acc:HGNC:813]"}, {"versioned_ensembl_gene_id":"ENSG00000226038.5","gene_symbol":"PPIAP21","gene_name":"peptidylprolyl isomerase A pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:16246]","synonyms":"PPIAL,dJ269M15.1","biotype":"processed_pseudogene","ncbi_id":"170536","summary":null,"start":43230760,"end":43231260,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:16246]"}, {"versioned_ensembl_gene_id":"ENSG00000270959.1","gene_symbol":"LPP-AS2","gene_name":"LPP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:27952]","synonyms":"MYCLo-6,MYCLo-5","biotype":"antisense_RNA","ncbi_id":"339929","summary":null,"start":188151206,"end":188154057,"strand":-1,"description":"LPP antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:27952]"}, {"versioned_ensembl_gene_id":"ENSG00000143776.18","gene_symbol":"CDC42BPA","gene_name":"CDC42 binding protein kinase alpha [Source:HGNC Symbol;Acc:HGNC:1737]","synonyms":"PK428,MRCKA,MRCK,KIAA0451,FLJ23347","biotype":"protein_coding","ncbi_id":"8476","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase contains multiple functional domains. Its kinase domain is highly similar to that of the myotonic dystrophy protein kinase (DMPK). This kinase also contains a Rac interactive binding (CRIB) domain, and has been shown to bind CDC42. It may function as a CDC42 downstream effector mediating CDC42 induced peripheral actin formation, and promoting cytoskeletal reorganization. Multiple alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2018]","start":226989865,"end":227318474,"strand":-1,"description":"CDC42 binding protein kinase alpha [Source:HGNC Symbol;Acc:HGNC:1737]"}, {"versioned_ensembl_gene_id":"ENSG00000145740.18","gene_symbol":"SLC30A5","gene_name":"solute carrier family 30 member 5 [Source:HGNC Symbol;Acc:HGNC:19089]","synonyms":"ZnT-5,MGC5499,FLJ12756,FLJ12496,ZTL1,ZNTL1,ZNT5","biotype":"protein_coding","ncbi_id":"64924","summary":"This gene encodes a member of the SLC30A/ZnT family of zinc transporter proteins. ZnT proteins mediate both cellular zinc efflux and zinc sequestration into membrane-bound organelles. The encoded protein plays a role in the early secretory pathway as a heterodimer with zinc transporter 6, and may also regulate zinc sequestration into secretory granules of pancreatic beta cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Oct 2011]","start":69093646,"end":69131069,"strand":1,"description":"solute carrier family 30 member 5 [Source:HGNC Symbol;Acc:HGNC:19089]"}, {"versioned_ensembl_gene_id":"ENSG00000198251.7","gene_symbol":"CYP2A7P2","gene_name":"cytochrome P450 family 2 subfamily A member 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2613]","synonyms":"CYP2A18PC","biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":40908480,"end":40910685,"strand":-1,"description":"cytochrome P450 family 2 subfamily A member 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2613]"}, {"versioned_ensembl_gene_id":"ENSG00000264790.1","gene_symbol":"AC021382.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27343252,"end":27346110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226884.1","gene_symbol":"RPS29P10","gene_name":"ribosomal protein S29 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132037","summary":null,"start":61589498,"end":61589663,"strand":-1,"description":"ribosomal protein S29 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37006]"}, {"versioned_ensembl_gene_id":"ENSG00000265555.1","gene_symbol":"LINC01903","gene_name":"long intergenic non-protein coding RNA 1903 [Source:HGNC Symbol;Acc:HGNC:52722]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927430","summary":null,"start":67808505,"end":67814822,"strand":-1,"description":"long intergenic non-protein coding RNA 1903 [Source:HGNC Symbol;Acc:HGNC:52722]"}, {"versioned_ensembl_gene_id":"ENSG00000264630.5","gene_symbol":"PRKCA-AS1","gene_name":"PRKCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51347]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928001","summary":null,"start":66398069,"end":66416854,"strand":-1,"description":"PRKCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51347]"}, {"versioned_ensembl_gene_id":"ENSG00000236007.1","gene_symbol":"MTCO1P46","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52111]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075175","summary":null,"start":211778273,"end":211779763,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52111]"}, {"versioned_ensembl_gene_id":"ENSG00000232631.1","gene_symbol":"MTND2P23","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42124]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873229","summary":null,"start":211777206,"end":211777856,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42124]"}, {"versioned_ensembl_gene_id":"ENSG00000273234.1","gene_symbol":"AC091768.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144142009,"end":144142938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136839.1","gene_symbol":"OR13C9","gene_name":"olfactory receptor family 13 subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:15104]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286362","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104617248,"end":104618204,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:15104]"}, {"versioned_ensembl_gene_id":"ENSG00000266588.1","gene_symbol":"AC006441.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39003248,"end":39013032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276119.1","gene_symbol":"OR13C2","gene_name":"olfactory receptor family 13 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:14701]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392376","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104604671,"end":104605627,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:14701]"}, {"versioned_ensembl_gene_id":"ENSG00000186943.1","gene_symbol":"OR13C8","gene_name":"olfactory receptor family 13 subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:15103]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138802","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104569168,"end":104570130,"strand":1,"description":"olfactory receptor family 13 subfamily C member 8 [Source:HGNC Symbol;Acc:HGNC:15103]"}, {"versioned_ensembl_gene_id":"ENSG00000276768.1","gene_symbol":"AL121890.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5049857,"end":5050321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237049.1","gene_symbol":"RPL34P1","gene_name":"ribosomal protein L34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10341]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"26514","summary":null,"start":168210616,"end":168210969,"strand":1,"description":"ribosomal protein L34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10341]"}, {"versioned_ensembl_gene_id":"ENSG00000240096.1","gene_symbol":"AL132838.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93223598,"end":93224139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267512.1","gene_symbol":"AC011446.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13139617,"end":13141147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239642.5","gene_symbol":"MEIKIN","gene_name":"meiotic kinetochore factor [Source:HGNC Symbol;Acc:HGNC:51253]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728637","summary":null,"start":131806993,"end":131945698,"strand":-1,"description":"meiotic kinetochore factor [Source:HGNC Symbol;Acc:HGNC:51253]"}, {"versioned_ensembl_gene_id":"ENSG00000225561.1","gene_symbol":"LINC01710","gene_name":"long intergenic non-protein coding RNA 1710 [Source:HGNC Symbol;Acc:HGNC:52498]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372925","summary":null,"start":218912757,"end":218916184,"strand":-1,"description":"long intergenic non-protein coding RNA 1710 [Source:HGNC Symbol;Acc:HGNC:52498]"}, {"versioned_ensembl_gene_id":"ENSG00000253651.1","gene_symbol":"SOD1P3","gene_name":"superoxide dismutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45136]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060005","summary":null,"start":125951861,"end":125952314,"strand":-1,"description":"superoxide dismutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45136]"}, {"versioned_ensembl_gene_id":"ENSG00000233532.5","gene_symbol":"LINC00460","gene_name":"long intergenic non-protein coding RNA 460 [Source:HGNC Symbol;Acc:HGNC:42809]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728192","summary":null,"start":106376563,"end":106378217,"strand":1,"description":"long intergenic non-protein coding RNA 460 [Source:HGNC Symbol;Acc:HGNC:42809]"}, {"versioned_ensembl_gene_id":"ENSG00000139163.15","gene_symbol":"ETNK1","gene_name":"ethanolamine kinase 1 [Source:HGNC Symbol;Acc:HGNC:24649]","synonyms":"EKI1,EKI","biotype":"protein_coding","ncbi_id":"55500","summary":"This gene encodes an ethanolamine kinase, which functions in the first committed step of the phosphatidylethanolamine synthesis pathway. This cytosolic enzyme is specific for ethanolamine and exhibits negligible kinase activity on choline. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":22625075,"end":22690665,"strand":1,"description":"ethanolamine kinase 1 [Source:HGNC Symbol;Acc:HGNC:24649]"}, {"versioned_ensembl_gene_id":"ENSG00000274885.1","gene_symbol":"AC087241.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22638464,"end":22638943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269945.1","gene_symbol":"AC004817.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71219100,"end":71222724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268886.1","gene_symbol":"AC022150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52575883,"end":52585561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072201.13","gene_symbol":"LNX1","gene_name":"ligand of numb-protein X 1 [Source:HGNC Symbol;Acc:HGNC:6657]","synonyms":"LNX,PDZRN2,MPDZ","biotype":"protein_coding","ncbi_id":"84708","summary":"This gene encodes a membrane-bound protein that is involved in signal transduction and protein interactions. The encoded product is an E3 ubiquitin-protein ligase, which mediates ubiquitination and subsequent proteasomal degradation of proteins containing phosphotyrosine binding (PTB) domains. This protein may play an important role in tumorogenesis. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene, which is located on chromosome 17, has been identified for this gene. [provided by RefSeq, Jul 2008]","start":53459301,"end":53701405,"strand":-1,"description":"ligand of numb-protein X 1 [Source:HGNC Symbol;Acc:HGNC:6657]"}, {"versioned_ensembl_gene_id":"ENSG00000163114.5","gene_symbol":"PDHA2","gene_name":"pyruvate dehydrogenase alpha 2 [Source:HGNC Symbol;Acc:HGNC:8807]","synonyms":"PDHAL","biotype":"protein_coding","ncbi_id":"5161","summary":null,"start":95840019,"end":95841474,"strand":1,"description":"pyruvate dehydrogenase alpha 2 [Source:HGNC Symbol;Acc:HGNC:8807]"}, {"versioned_ensembl_gene_id":"ENSG00000251034.1","gene_symbol":"AC037459.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22540845,"end":22545405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177398.18","gene_symbol":"UMODL1","gene_name":"uromodulin like 1 [Source:HGNC Symbol;Acc:HGNC:12560]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89766","summary":null,"start":42062959,"end":42143453,"strand":1,"description":"uromodulin like 1 [Source:HGNC Symbol;Acc:HGNC:12560]"}, {"versioned_ensembl_gene_id":"ENSG00000249971.1","gene_symbol":"AC104116.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138347027,"end":138349641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218890.1","gene_symbol":"AL049842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66093431,"end":66094909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279584.1","gene_symbol":"AC005593.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131797415,"end":131797929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230417.11","gene_symbol":"LINC00595","gene_name":"long intergenic non-protein coding RNA 595 [Source:HGNC Symbol;Acc:HGNC:31430]","synonyms":"C10orf101","biotype":"lincRNA","ncbi_id":"414243","summary":null,"start":78179185,"end":78551355,"strand":1,"description":"long intergenic non-protein coding RNA 595 [Source:HGNC Symbol;Acc:HGNC:31430]"}, {"versioned_ensembl_gene_id":"ENSG00000113282.13","gene_symbol":"CLINT1","gene_name":"clathrin interactor 1 [Source:HGNC Symbol;Acc:HGNC:23186]","synonyms":"KIAA0171,EPNR,ENTH,CLINT","biotype":"protein_coding","ncbi_id":"9685","summary":"This gene encodes a protein with similarity to the epsin family of endocytic adapter proteins. The encoded protein interacts with clathrin, the adapter protein AP-1 and phosphoinositides. This protein may be involved in the formation of clathrin coated vesicles and trafficking between the trans-Golgi network and endosomes. Mutations in this gene are associated with a susceptibility to schizophrenia and psychotic disorders. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":157785743,"end":157859175,"strand":-1,"description":"clathrin interactor 1 [Source:HGNC Symbol;Acc:HGNC:23186]"}, {"versioned_ensembl_gene_id":"ENSG00000063177.12","gene_symbol":"RPL18","gene_name":"ribosomal protein L18 [Source:HGNC Symbol;Acc:HGNC:10310]","synonyms":"L18","biotype":"protein_coding","ncbi_id":"6141","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18E family of ribosomal proteins that is a component of the 60S subunit. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":48615328,"end":48619536,"strand":-1,"description":"ribosomal protein L18 [Source:HGNC Symbol;Acc:HGNC:10310]"}, {"versioned_ensembl_gene_id":"ENSG00000226750.1","gene_symbol":"AL360271.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":242345558,"end":242345718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234586.2","gene_symbol":"AL161449.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13021694,"end":13022892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180287.16","gene_symbol":"PLD5","gene_name":"phospholipase D family member 5 [Source:HGNC Symbol;Acc:HGNC:26879]","synonyms":"FLJ40773","biotype":"protein_coding","ncbi_id":"200150","summary":null,"start":242082986,"end":242524696,"strand":-1,"description":"phospholipase D family member 5 [Source:HGNC Symbol;Acc:HGNC:26879]"}, {"versioned_ensembl_gene_id":"ENSG00000255540.1","gene_symbol":"AP003122.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89731017,"end":89734782,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255486.1","gene_symbol":"AP003122.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89723482,"end":89727253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168228.14","gene_symbol":"ZCCHC4","gene_name":"zinc finger CCHC-type containing 4 [Source:HGNC Symbol;Acc:HGNC:22917]","synonyms":"ZGRF4,HSPC052,FLJ23024","biotype":"protein_coding","ncbi_id":"29063","summary":null,"start":25312785,"end":25370383,"strand":1,"description":"zinc finger CCHC-type containing 4 [Source:HGNC Symbol;Acc:HGNC:22917]"}, {"versioned_ensembl_gene_id":"ENSG00000108405.3","gene_symbol":"P2RX1","gene_name":"purinergic receptor P2X 1 [Source:HGNC Symbol;Acc:HGNC:8533]","synonyms":"P2X1","biotype":"protein_coding","ncbi_id":"5023","summary":"The protein encoded by this gene belongs to the P2X family of G-protein-coupled receptors. These proteins can form homo-and heterotimers and function as ATP-gated ion channels and mediate rapid and selective permeability to cations. This protein is primarily localized to smooth muscle where binds ATP and mediates synaptic transmission between neurons and from neurons to smooth muscle and may being responsible for sympathetic vasoconstriction in small arteries, arterioles and vas deferens. Mouse studies suggest that this receptor is essential for normal male reproductive function. This protein may also be involved in promoting apoptosis. [provided by RefSeq, Jun 2013]","start":3896592,"end":3916500,"strand":-1,"description":"purinergic receptor P2X 1 [Source:HGNC Symbol;Acc:HGNC:8533]"}, {"versioned_ensembl_gene_id":"ENSG00000127084.17","gene_symbol":"FGD3","gene_name":"FYVE, RhoGEF and PH domain containing 3 [Source:HGNC Symbol;Acc:HGNC:16027]","synonyms":"ZFYVE5,FLJ00004","biotype":"protein_coding","ncbi_id":"89846","summary":null,"start":92947451,"end":93036236,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 3 [Source:HGNC Symbol;Acc:HGNC:16027]"}, {"versioned_ensembl_gene_id":"ENSG00000145439.11","gene_symbol":"CBR4","gene_name":"carbonyl reductase 4 [Source:HGNC Symbol;Acc:HGNC:25891]","synonyms":"SDR45C1,FLJ14431","biotype":"protein_coding","ncbi_id":"84869","summary":null,"start":168863770,"end":169010275,"strand":-1,"description":"carbonyl reductase 4 [Source:HGNC Symbol;Acc:HGNC:25891]"}, {"versioned_ensembl_gene_id":"ENSG00000250594.2","gene_symbol":"AC108145.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110264865,"end":110265017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279163.1","gene_symbol":"AP003122.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89704164,"end":89704658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258890.6","gene_symbol":"CEP95","gene_name":"centrosomal protein 95 [Source:HGNC Symbol;Acc:HGNC:25141]","synonyms":"DKFZp667E1824,CCDC45","biotype":"protein_coding","ncbi_id":"90799","summary":null,"start":64506588,"end":64542461,"strand":1,"description":"centrosomal protein 95 [Source:HGNC Symbol;Acc:HGNC:25141]"}, {"versioned_ensembl_gene_id":"ENSG00000274629.1","gene_symbol":"AC073052.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":224464682,"end":224474500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254789.2","gene_symbol":"AC073172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15571819,"end":15622403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280426.1","gene_symbol":"AC084876.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":109997419,"end":109999127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229962.1","gene_symbol":"AP000221.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25515473,"end":25518338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230508.1","gene_symbol":"RPL19P21","gene_name":"ribosomal protein L19 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35868]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392557","summary":null,"start":150993501,"end":150994091,"strand":1,"description":"ribosomal protein L19 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35868]"}, {"versioned_ensembl_gene_id":"ENSG00000258770.1","gene_symbol":"LINC02330","gene_name":"long intergenic non-protein coding RNA 2330 [Source:HGNC Symbol;Acc:HGNC:53250]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370611","summary":null,"start":87634379,"end":87655294,"strand":-1,"description":"long intergenic non-protein coding RNA 2330 [Source:HGNC Symbol;Acc:HGNC:53250]"}, {"versioned_ensembl_gene_id":"ENSG00000099814.15","gene_symbol":"CEP170B","gene_name":"centrosomal protein 170B [Source:HGNC Symbol;Acc:HGNC:20362]","synonyms":"KIAA0284,FAM68C,Cep170R","biotype":"protein_coding","ncbi_id":"283638","summary":null,"start":104865280,"end":104896770,"strand":1,"description":"centrosomal protein 170B [Source:HGNC Symbol;Acc:HGNC:20362]"}, {"versioned_ensembl_gene_id":"ENSG00000157322.17","gene_symbol":"CLEC18A","gene_name":"C-type lectin domain family 18 member A [Source:HGNC Symbol;Acc:HGNC:30388]","synonyms":"MRCL","biotype":"protein_coding","ncbi_id":"348174","summary":"This is one of three closely related paralogous genes on chromosome 16 encoding secreted proteins containing C-type lectin domains. These domains bind to carbohydrates in the presence of calcium, and may be involved in cell adhesion, immune response and apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012]","start":69950705,"end":69964452,"strand":1,"description":"C-type lectin domain family 18 member A [Source:HGNC Symbol;Acc:HGNC:30388]"}, {"versioned_ensembl_gene_id":"ENSG00000213236.3","gene_symbol":"YWHAZP2","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31078]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"150554","summary":null,"start":126557435,"end":126558162,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31078]"}, {"versioned_ensembl_gene_id":"ENSG00000254577.1","gene_symbol":"AC087276.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":43390283,"end":43395495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000094880.10","gene_symbol":"CDC23","gene_name":"cell division cycle 23 [Source:HGNC Symbol;Acc:HGNC:1724]","synonyms":"CUT23,APC8,ANAPC8","biotype":"protein_coding","ncbi_id":"8697","summary":"The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. [provided by RefSeq, Jul 2008]","start":138187648,"end":138213343,"strand":-1,"description":"cell division cycle 23 [Source:HGNC Symbol;Acc:HGNC:1724]"}, {"versioned_ensembl_gene_id":"ENSG00000231470.1","gene_symbol":"HMGB3P2","gene_name":"high mobility group box 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16574]","synonyms":"HMGB3L2,HMG4L2,dJ550H1.1","biotype":"processed_pseudogene","ncbi_id":"128879","summary":null,"start":36076018,"end":36076601,"strand":-1,"description":"high mobility group box 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16574]"}, {"versioned_ensembl_gene_id":"ENSG00000230280.2","gene_symbol":"HNRNPA1P59","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:48789]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730246","summary":null,"start":202911812,"end":202912729,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:48789]"}, {"versioned_ensembl_gene_id":"ENSG00000230153.5","gene_symbol":"AF274573.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150915813,"end":150920938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234146.1","gene_symbol":"AKAP8P1","gene_name":"A-kinase anchoring protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49758]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646114","summary":null,"start":11011748,"end":11013096,"strand":1,"description":"A-kinase anchoring protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49758]"}, {"versioned_ensembl_gene_id":"ENSG00000178607.15","gene_symbol":"ERN1","gene_name":"endoplasmic reticulum to nucleus signaling 1 [Source:HGNC Symbol;Acc:HGNC:3449]","synonyms":"IRE1P,IRE1","biotype":"protein_coding","ncbi_id":"2081","summary":"This gene encodes the transmembrane protein kinase inositol-requiring enzyme 1. The encoded protein contains two functional catalytic domains, a serine/threonine-protein kinase domain and an endoribonuclease domain. This protein functions as a sensor of unfolded proteins in the endoplasmic reticulum (ER) and triggers an intracellular signaling pathway termed the unfolded protein response (UPR). The UPR is an ER stress response that is conserved from yeast to mammals and activates genes involved in degrading misfolded proteins, regulating protein synthesis and activating molecular chaperones. This protein specifically mediates the splicing and activation of the stress response transcription factor X-box binding protein 1. [provided by RefSeq, Aug 2017]","start":64039142,"end":64130819,"strand":-1,"description":"endoplasmic reticulum to nucleus signaling 1 [Source:HGNC Symbol;Acc:HGNC:3449]"}, {"versioned_ensembl_gene_id":"ENSG00000279170.1","gene_symbol":"AL137784.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":99587611,"end":99589898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232100.1","gene_symbol":"LINC01653","gene_name":"long intergenic non-protein coding RNA 1653 [Source:HGNC Symbol;Acc:HGNC:52441]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929631","summary":null,"start":218043505,"end":218059140,"strand":1,"description":"long intergenic non-protein coding RNA 1653 [Source:HGNC Symbol;Acc:HGNC:52441]"}, {"versioned_ensembl_gene_id":"ENSG00000221995.5","gene_symbol":"TIAF1","gene_name":"TGFB1-induced anti-apoptotic factor 1 [Source:HGNC Symbol;Acc:HGNC:11803]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9220","summary":null,"start":29073521,"end":29078857,"strand":-1,"description":"TGFB1-induced anti-apoptotic factor 1 [Source:HGNC Symbol;Acc:HGNC:11803]"}, {"versioned_ensembl_gene_id":"ENSG00000249169.1","gene_symbol":"AC026780.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92654848,"end":92679141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255088.1","gene_symbol":"AC013828.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13758111,"end":13758345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249776.5","gene_symbol":"AC124854.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92410256,"end":92660863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236800.1","gene_symbol":"AC068898.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48664199,"end":48672424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248826.2","gene_symbol":"PCBP2P3","gene_name":"poly(rC) binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131236","summary":null,"start":91843687,"end":91844529,"strand":-1,"description":"poly(rC) binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39032]"}, {"versioned_ensembl_gene_id":"ENSG00000256001.1","gene_symbol":"AC079949.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127145072,"end":127146532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259047.1","gene_symbol":"AL163153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42989201,"end":42989483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177243.3","gene_symbol":"DEFB103B","gene_name":"defensin beta 103B [Source:HGNC Symbol;Acc:HGNC:31702]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55894","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 103, which has broad spectrum antimicrobial activity and may play an important role in innate epithelial defense. [provided by RefSeq, Oct 2014]","start":7428888,"end":7430348,"strand":-1,"description":"defensin beta 103B [Source:HGNC Symbol;Acc:HGNC:31702]"}, {"versioned_ensembl_gene_id":"ENSG00000224383.7","gene_symbol":"PRR29","gene_name":"proline rich 29 [Source:HGNC Symbol;Acc:HGNC:25673]","synonyms":"DKFZp761M2312,C17orf72,FLJ11724","biotype":"protein_coding","ncbi_id":"92340","summary":null,"start":63998351,"end":64004304,"strand":1,"description":"proline rich 29 [Source:HGNC Symbol;Acc:HGNC:25673]"}, {"versioned_ensembl_gene_id":"ENSG00000167394.12","gene_symbol":"ZNF668","gene_name":"zinc finger protein 668 [Source:HGNC Symbol;Acc:HGNC:25821]","synonyms":"FLJ13479","biotype":"protein_coding","ncbi_id":"79759","summary":null,"start":31060843,"end":31074320,"strand":-1,"description":"zinc finger protein 668 [Source:HGNC Symbol;Acc:HGNC:25821]"}, {"versioned_ensembl_gene_id":"ENSG00000262484.1","gene_symbol":"CCER2","gene_name":"coiled-coil glutamate rich protein 2 [Source:HGNC Symbol;Acc:HGNC:44662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643669","summary":null,"start":38908980,"end":38912158,"strand":-1,"description":"coiled-coil glutamate rich protein 2 [Source:HGNC Symbol;Acc:HGNC:44662]"}, {"versioned_ensembl_gene_id":"ENSG00000172586.7","gene_symbol":"CHCHD1","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23518]","synonyms":"C10orf34,FLJ25854","biotype":"protein_coding","ncbi_id":"118487","summary":null,"start":73782047,"end":73783652,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23518]"}, {"versioned_ensembl_gene_id":"ENSG00000262454.3","gene_symbol":"MIR193BHG","gene_name":"MIR193B host gene [Source:HGNC Symbol;Acc:HGNC:51945]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129781","summary":null,"start":14301389,"end":14331067,"strand":1,"description":"MIR193B host gene [Source:HGNC Symbol;Acc:HGNC:51945]"}, {"versioned_ensembl_gene_id":"ENSG00000163344.5","gene_symbol":"PMVK","gene_name":"phosphomevalonate kinase [Source:HGNC Symbol;Acc:HGNC:9141]","synonyms":"PMKA,PMK,HUMPMKI","biotype":"protein_coding","ncbi_id":"10654","summary":"This gene encodes a peroxisomal enzyme that is a member of the galactokinase, homoserine kinase, mevalonate kinase, and phosphomevalonate kinase (GHMP) family of ATP-dependent enzymes. The encoded protein catalyzes the conversion of mevalonate 5-phosphate to mevalonate 5-diphosphate, which is the fifth step in the mevalonate pathway of isoprenoid biosynthesis. Mutations in this gene are linked to certain types of porokeratosis including disseminated superficial porokeratosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":154924734,"end":154936991,"strand":-1,"description":"phosphomevalonate kinase [Source:HGNC Symbol;Acc:HGNC:9141]"}, {"versioned_ensembl_gene_id":"ENSG00000256243.2","gene_symbol":"AL121594.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35235180,"end":35235651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276707.1","gene_symbol":"AC243773.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36940049,"end":36943456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227460.8","gene_symbol":"SYNGAP1","gene_name":"synaptic Ras GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:11497]","synonyms":"KIAA1938,SYNGAP,RASA5","biotype":"protein_coding","ncbi_id":"8831","summary":"This gene encodes a Ras GTPase activating protein that is a member of the N-methyl-D-aspartate receptor complex. The N-terminal domain of the protein contains a Ras-GAP domain, a pleckstrin homology domain, and a C2 domain that may be involved in binding of calcium and phospholipids. The C-terminal domain consists of a ten histidine repeat region, serine and tyrosine phosphorylation sites, and a T/SXV motif required for postsynaptic scaffold protein interaction. The encoded protein negatively regulates Ras, Rap and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking to the postsynaptic membrane to regulate synaptic plasticity and neuronal homeostasis. Allelic variants of this gene are associated with intellectual disability and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":33560260,"end":33593877,"strand":1,"description":"synaptic Ras GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:11497]"}, {"versioned_ensembl_gene_id":"ENSG00000234363.1","gene_symbol":"PPIAP27","gene_name":"peptidylprolyl isomerase A pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874405","summary":null,"start":20956179,"end":20956443,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42646]"}, {"versioned_ensembl_gene_id":"ENSG00000277013.1","gene_symbol":"AC008556.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33906352,"end":33908391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254495.1","gene_symbol":"AP000487.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70358198,"end":70358677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245556.2","gene_symbol":"SCAMP1-AS1","gene_name":"SCAMP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50544]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728769","summary":null,"start":78342365,"end":78360507,"strand":-1,"description":"SCAMP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50544]"}, {"versioned_ensembl_gene_id":"ENSG00000255539.1","gene_symbol":"AP002336.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70324871,"end":70327209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282353.1","gene_symbol":"AC234635.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142370836,"end":142371348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077616.10","gene_symbol":"NAALAD2","gene_name":"N-acetylated alpha-linked acidic dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:14526]","synonyms":"NAALADASE2,GCPIII","biotype":"protein_coding","ncbi_id":"10003","summary":"This gene is a member of the N-acetylated alpha-linked acidic dipeptidase (NAALADase) gene family. The representative member of this family is the gene encoding human prostate-specific membrane antigen (PSM), which is a marker of prostatic carcinomas and is the first to be shown to possess NAALADase activity. NAALADase cleaves N-acetyl-L-aspartate-L-glutamate (NAAG), which is a neuropeptide expressed both in the central nervous systems and in the periphery and is thought to function as a neurotransmitter. The product of this gene is a type II integral membrane protein. Transient transfection of this gene confers both NAALADase and dipetidyl peptidase IV activities to mammalian cells. This gene is highly expressed in ovary and testis as well as within discrete brain areas. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":90131515,"end":90192894,"strand":1,"description":"N-acetylated alpha-linked acidic dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:14526]"}, {"versioned_ensembl_gene_id":"ENSG00000155846.16","gene_symbol":"PPARGC1B","gene_name":"PPARG coactivator 1 beta [Source:HGNC Symbol;Acc:HGNC:30022]","synonyms":"PERC,PGC1B","biotype":"protein_coding","ncbi_id":"133522","summary":"The protein encoded by this gene stimulates the activity of several transcription factors and nuclear receptors, including estrogen receptor alpha, nuclear respiratory factor 1, and glucocorticoid receptor. The encoded protein may be involved in fat oxidation, non-oxidative glucose metabolism, and the regulation of energy expenditure. This protein is downregulated in prediabetic and type 2 diabetes mellitus patients. Certain allelic variations in this gene increase the risk of the development of obesity. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":149730298,"end":149855022,"strand":1,"description":"PPARG coactivator 1 beta [Source:HGNC Symbol;Acc:HGNC:30022]"}, {"versioned_ensembl_gene_id":"ENSG00000250834.1","gene_symbol":"KRT18P54","gene_name":"keratin 18 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:39425]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418792","summary":null,"start":135371177,"end":135371924,"strand":-1,"description":"keratin 18 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:39425]"}, {"versioned_ensembl_gene_id":"ENSG00000248104.1","gene_symbol":"TARS2P1","gene_name":"threonyl-tRNA synthetase 2, mitochondrial (putative) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43712]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533844","summary":null,"start":135565117,"end":135567157,"strand":-1,"description":"threonyl-tRNA synthetase 2, mitochondrial (putative) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43712]"}, {"versioned_ensembl_gene_id":"ENSG00000162670.10","gene_symbol":"BRINP3","gene_name":"BMP/retinoic acid inducible neural specific 3 [Source:HGNC Symbol;Acc:HGNC:22393]","synonyms":"FAM5C,DBCCR1L1,DBCCR1L","biotype":"protein_coding","ncbi_id":"339479","summary":"This gene is overexpressed in pituitary tumors but is underexpressed in tongue squamous cell carcinomas, ulcerative colitis, and peri-implantitis. Polymorphisms that increase expression of this gene have been shown to increase vascular inflammation, and an association of this gene with myocardial infarction has been demonstrated. Finally, hypermethylation of this gene may find usefulness as a biomarker for gastric cancer. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":190097662,"end":190478404,"strand":-1,"description":"BMP/retinoic acid inducible neural specific 3 [Source:HGNC Symbol;Acc:HGNC:22393]"}, {"versioned_ensembl_gene_id":"ENSG00000250338.1","gene_symbol":"AC095057.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40265472,"end":40266457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213174.3","gene_symbol":"AC026316.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170653846,"end":170654259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244278.1","gene_symbol":"AP000235.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25055535,"end":25069906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171222.10","gene_symbol":"SCAND1","gene_name":"SCAN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:10566]","synonyms":"SDP1,RAZ1","biotype":"protein_coding","ncbi_id":"51282","summary":"This gene encodes a SCAN box domain-containing protein. The SCAN domain is a highly conserved, leucine-rich motif of approximately 60 aa originally found within a subfamily of zinc finger proteins. This gene belongs to a family of genes that encode an isolated SCAN domain, but no zinc finger motif. This protein binds to and may regulate the function of the transcription factor myeloid zinc finger 1B. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]","start":35953617,"end":35959472,"strand":-1,"description":"SCAN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:10566]"}, {"versioned_ensembl_gene_id":"ENSG00000258718.1","gene_symbol":"LINC02311","gene_name":"long intergenic non-protein coding RNA 2311 [Source:HGNC Symbol;Acc:HGNC:53230]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724294","summary":null,"start":81727780,"end":81743138,"strand":-1,"description":"long intergenic non-protein coding RNA 2311 [Source:HGNC Symbol;Acc:HGNC:53230]"}, {"versioned_ensembl_gene_id":"ENSG00000139350.11","gene_symbol":"NEDD1","gene_name":"neural precursor cell expressed, developmentally down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:7723]","synonyms":"TUBGCP7,GCP-WD","biotype":"protein_coding","ncbi_id":"121441","summary":null,"start":96907223,"end":96953777,"strand":1,"description":"neural precursor cell expressed, developmentally down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:7723]"}, {"versioned_ensembl_gene_id":"ENSG00000132300.18","gene_symbol":"PTCD3","gene_name":"pentatricopeptide repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:24717]","synonyms":"FLJ20758,DKFZp666K071","biotype":"protein_coding","ncbi_id":"55037","summary":null,"start":86106182,"end":86142157,"strand":1,"description":"pentatricopeptide repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:24717]"}, {"versioned_ensembl_gene_id":"ENSG00000130766.4","gene_symbol":"SESN2","gene_name":"sestrin 2 [Source:HGNC Symbol;Acc:HGNC:20746]","synonyms":"HI95,DKFZp761M0212,SEST2,SES2","biotype":"protein_coding","ncbi_id":"83667","summary":"This gene encodes a member of the sestrin family of PA26-related proteins. The encoded protein may function in the regulation of cell growth and survival. This protein may be involved in cellular response to different stress conditions. [provided by RefSeq, Jul 2008]","start":28259527,"end":28282491,"strand":1,"description":"sestrin 2 [Source:HGNC Symbol;Acc:HGNC:20746]"}, {"versioned_ensembl_gene_id":"ENSG00000255065.1","gene_symbol":"AP002001.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106310045,"end":106311791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227948.4","gene_symbol":"AC003989.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111411319,"end":111411883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248103.1","gene_symbol":"AC008443.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181281375,"end":181283652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237481.1","gene_symbol":"AL117350.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":229319403,"end":229323087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111331.12","gene_symbol":"OAS3","gene_name":"2'-5'-oligoadenylate synthetase 3 [Source:HGNC Symbol;Acc:HGNC:8088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4940","summary":"This gene encodes an enzyme included in the 2', 5' oligoadenylate synthase family. This enzyme is induced by interferons and catalyzes the 2', 5' oligomers of adenosine in order to bind and activate RNase L. This enzyme family plays a significant role in the inhibition of cellular protein synthesis and viral infection resistance. [provided by RefSeq, Jul 2008]","start":112938352,"end":112973249,"strand":1,"description":"2'-5'-oligoadenylate synthetase 3 [Source:HGNC Symbol;Acc:HGNC:8088]"}, {"versioned_ensembl_gene_id":"ENSG00000225006.1","gene_symbol":"AL929288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188508538,"end":188536465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167088.10","gene_symbol":"SNRPD1","gene_name":"small nuclear ribonucleoprotein D1 polypeptide [Source:HGNC Symbol;Acc:HGNC:11158]","synonyms":"SNRPD,Sm-D1,HsT2456","biotype":"protein_coding","ncbi_id":"6632","summary":"This gene encodes a small nuclear ribonucleoprotein that belongs to the SNRNP core protein family. The protein may act as a charged protein scaffold to promote SNRNP assembly or strengthen SNRNP-SNRNP interactions through nonspecific electrostatic contacts with RNA. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":21612267,"end":21633524,"strand":1,"description":"small nuclear ribonucleoprotein D1 polypeptide [Source:HGNC Symbol;Acc:HGNC:11158]"}, {"versioned_ensembl_gene_id":"ENSG00000283667.1","gene_symbol":"AC009802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63966406,"end":63970181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170545.16","gene_symbol":"SMAGP","gene_name":"small cell adhesion glycoprotein [Source:HGNC Symbol;Acc:HGNC:26918]","synonyms":"MGC149453,hSMAGP,MGC149454","biotype":"protein_coding","ncbi_id":"57228","summary":null,"start":51244558,"end":51270890,"strand":-1,"description":"small cell adhesion glycoprotein [Source:HGNC Symbol;Acc:HGNC:26918]"}, {"versioned_ensembl_gene_id":"ENSG00000159618.15","gene_symbol":"ADGRG5","gene_name":"adhesion G protein-coupled receptor G5 [Source:HGNC Symbol;Acc:HGNC:19010]","synonyms":"PGR27,GPR114","biotype":"protein_coding","ncbi_id":"221188","summary":"This gene encodes a member of the adhesion family of G-protein coupled receptors. Members of this family are characterized by long N-termini and multiple functional domains. They may play a role in the immune system as well as in the central nervous system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":57542421,"end":57591681,"strand":1,"description":"adhesion G protein-coupled receptor G5 [Source:HGNC Symbol;Acc:HGNC:19010]"}, {"versioned_ensembl_gene_id":"ENSG00000257452.1","gene_symbol":"AC004551.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112907628,"end":113017751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107821.14","gene_symbol":"KAZALD1","gene_name":"Kazal type serine peptidase inhibitor domain 1 [Source:HGNC Symbol;Acc:HGNC:25460]","synonyms":"FKSG40,FKSG28","biotype":"protein_coding","ncbi_id":"81621","summary":"This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":101061841,"end":101068131,"strand":1,"description":"Kazal type serine peptidase inhibitor domain 1 [Source:HGNC Symbol;Acc:HGNC:25460]"}, {"versioned_ensembl_gene_id":"ENSG00000236372.1","gene_symbol":"AL353052.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":232174932,"end":232180113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184260.5","gene_symbol":"HIST2H2AC","gene_name":"histone cluster 2 H2A family member c [Source:HGNC Symbol;Acc:HGNC:4738]","synonyms":"H2AFQ,H2A/q,H2A","biotype":"protein_coding","ncbi_id":"8338","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. [provided by RefSeq, Aug 2015]","start":149886975,"end":149887364,"strand":1,"description":"histone cluster 2 H2A family member c [Source:HGNC Symbol;Acc:HGNC:4738]"}, {"versioned_ensembl_gene_id":"ENSG00000250762.1","gene_symbol":"Z99943.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":167819898,"end":167820248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282573.1","gene_symbol":"AC100803.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141353403,"end":141355365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198553.8","gene_symbol":"KCNRG","gene_name":"potassium channel regulator [Source:HGNC Symbol;Acc:HGNC:18893]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283518","summary":"This gene encodes a protein which regulates the activity of voltage-gated potassium channels. This gene is on chromosome 13 and overlaps the gene for tripartite motif containing 13 on the same strand. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":50015254,"end":50020922,"strand":1,"description":"potassium channel regulator [Source:HGNC Symbol;Acc:HGNC:18893]"}, {"versioned_ensembl_gene_id":"ENSG00000140992.18","gene_symbol":"PDPK1","gene_name":"3-phosphoinositide dependent protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:8816]","synonyms":"PDK1","biotype":"protein_coding","ncbi_id":"5170","summary":null,"start":2537964,"end":2603188,"strand":1,"description":"3-phosphoinositide dependent protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:8816]"}, {"versioned_ensembl_gene_id":"ENSG00000261093.1","gene_symbol":"AC141586.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2597881,"end":2599718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233937.6","gene_symbol":"AC008443.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":181246523,"end":181272167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266844.1","gene_symbol":"AC093330.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76974690,"end":76984162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282363.1","gene_symbol":"AC006518.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":10894943,"end":10896952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204469.12","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"BAT2,G2,D6S51E","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31620720,"end":31637771,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000239716.1","gene_symbol":"AC079943.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157976561,"end":157978136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127578.6","gene_symbol":"WFIKKN1","gene_name":"WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30912]","synonyms":"WFIKKN,WFDC20A,RJD2,C16orf12","biotype":"protein_coding","ncbi_id":"117166","summary":"This gene encodes a secreted multidomain protein consisting of a signal peptide, a WAP domain, a follistatin domain, an immunoglobulin domain, two tandem Kunitz domains, and an NTR domain. These domains have been implicated frequently in inhibition of various types of proteases, suggesting that the encoded protein may be a multivalent protease inhibitor and may control the action of multiple types of serine proteases as well as metalloproteinases. [provided by RefSeq, Jul 2008]","start":629239,"end":634116,"strand":1,"description":"WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30912]"}, {"versioned_ensembl_gene_id":"ENSG00000234901.1","gene_symbol":"MTND6P13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39476]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480428","summary":null,"start":102008524,"end":102009046,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39476]"}, {"versioned_ensembl_gene_id":"ENSG00000227277.9","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"G16,RING5,RMA1,NG2","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32186026,"end":32188465,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000250566.1","gene_symbol":"UGT2B29P","gene_name":"UDP glucuronosyltransferase family 2 member B29, pseudogene [Source:HGNC Symbol;Acc:HGNC:12552]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"54568","summary":null,"start":68509441,"end":68517647,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B29, pseudogene [Source:HGNC Symbol;Acc:HGNC:12552]"}, {"versioned_ensembl_gene_id":"ENSG00000275454.1","gene_symbol":"AC105020.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75639760,"end":75640976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151929.9","gene_symbol":"BAG3","gene_name":"BCL2 associated athanogene 3 [Source:HGNC Symbol;Acc:HGNC:939]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9531","summary":"BAG proteins compete with Hip for binding to the Hsc70/Hsp70 ATPase domain and promote substrate release. All the BAG proteins have an approximately 45-amino acid BAG domain near the C terminus but differ markedly in their N-terminal regions. The protein encoded by this gene contains a WW domain in the N-terminal region and a BAG domain in the C-terminal region. The BAG domains of BAG1, BAG2, and BAG3 interact specifically with the Hsc70 ATPase domain in vitro and in mammalian cells. All 3 proteins bind with high affinity to the ATPase domain of Hsc70 and inhibit its chaperone activity in a Hip-repressible manner. [provided by RefSeq, Jul 2008]","start":119651370,"end":119677819,"strand":1,"description":"BCL2 associated athanogene 3 [Source:HGNC Symbol;Acc:HGNC:939]"}, {"versioned_ensembl_gene_id":"ENSG00000244313.3","gene_symbol":"AC024293.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46428653,"end":46429150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274702.1","gene_symbol":"AL357559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187632166,"end":187632439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236766.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30692927,"end":30703043,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000224587.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"Em:AB023051.5,NFBD1,KIAA0170","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30689666,"end":30707748,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000205129.8","gene_symbol":"C4orf47","gene_name":"chromosome 4 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:34346]","synonyms":"LOC441054","biotype":"protein_coding","ncbi_id":"441054","summary":null,"start":185426249,"end":185449826,"strand":1,"description":"chromosome 4 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:34346]"}, {"versioned_ensembl_gene_id":"ENSG00000177770.11","gene_symbol":"CDKN2AIPNLP1","gene_name":"CDKN2A interacting protein N-terminal like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39854]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391169","summary":null,"start":226493188,"end":226493489,"strand":-1,"description":"CDKN2A interacting protein N-terminal like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39854]"}, {"versioned_ensembl_gene_id":"ENSG00000137628.16","gene_symbol":"DDX60","gene_name":"DExD/H-box helicase 60 [Source:HGNC Symbol;Acc:HGNC:25942]","synonyms":"FLJ20035","biotype":"protein_coding","ncbi_id":"55601","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases which are implicated in a number of cellular procsses involving RNA binding and alteration of RNA secondary structure. This gene encodes a DEXD/H box RNA helicase that functions as an antiviral factor and promotes RIG-I-like receptor-mediated signaling. [provided by RefSeq, Apr 2017]","start":168216293,"end":168318807,"strand":-1,"description":"DExD/H-box helicase 60 [Source:HGNC Symbol;Acc:HGNC:25942]"}, {"versioned_ensembl_gene_id":"ENSG00000253618.1","gene_symbol":"GRPEL2-AS1","gene_name":"GRPEL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48999]","synonyms":"RP11-394O4.4","biotype":"antisense_RNA","ncbi_id":"106144529","summary":null,"start":149348116,"end":149357642,"strand":-1,"description":"GRPEL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48999]"}, {"versioned_ensembl_gene_id":"ENSG00000248369.1","gene_symbol":"AC114741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132435802,"end":132447235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228099.3","gene_symbol":"RPL12P1","gene_name":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]","synonyms":"RPL12-L,dJ570F3.5,CICK0721Q.1","biotype":"processed_pseudogene","ncbi_id":"729727","summary":null,"start":33328865,"end":33329362,"strand":-1,"description":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]"}, {"versioned_ensembl_gene_id":"ENSG00000226059.2","gene_symbol":"HMGB3P20","gene_name":"high mobility group box 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39312]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442661","summary":null,"start":26982768,"end":26983367,"strand":-1,"description":"high mobility group box 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39312]"}, {"versioned_ensembl_gene_id":"ENSG00000213787.3","gene_symbol":"AC073472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26922110,"end":26922912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139718.10","gene_symbol":"SETD1B","gene_name":"SET domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29187]","synonyms":"Set1B,KMT2G,KIAA1076","biotype":"protein_coding","ncbi_id":"23067","summary":"SET1B is a component of a histone methyltransferase complex that produces trimethylated histone H3 at Lys4 (Lee et al., 2007 [PubMed 17355966]).[supplied by OMIM, Mar 2008]","start":121804180,"end":121832584,"strand":1,"description":"SET domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29187]"}, {"versioned_ensembl_gene_id":"ENSG00000282803.1","gene_symbol":"TRBV5-1","gene_name":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]","synonyms":"TCRBV5S1A1T,TCRBV5S1,TRBV51","biotype":"TR_V_gene","ncbi_id":"28614","summary":null,"start":142320696,"end":142321563,"strand":1,"description":"T-cell receptor beta variable 5-1 [Source:HGNC Symbol;Acc:HGNC:12218]"}, {"versioned_ensembl_gene_id":"ENSG00000283542.1","gene_symbol":"AC079602.4","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":121053732,"end":121059670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223484.7","gene_symbol":"TRPC6P","gene_name":"transient receptor potential cation channel subfamily C member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:23270]","synonyms":"TRPC6L","biotype":"processed_pseudogene","ncbi_id":"644218","summary":null,"start":155985370,"end":155986249,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:23270]"}, {"versioned_ensembl_gene_id":"ENSG00000231210.2","gene_symbol":"LINC01510","gene_name":"long intergenic non-protein coding RNA 1510 [Source:HGNC Symbol;Acc:HGNC:51196]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996266","summary":"This gene encodes a natural antisense transcript highly expressed in papillary thyroid carcinomas harboring BRAF V600E mutation or RET gene rearrangements. This lncRNA induces the downstream MAPK pathway and is part of a co-expression network including different oncogenes belonging to the MAPK and PI3H/AKT pathways. In thyroid carcinomas, this gene has oncogenic properties associated with increased proliferation and drug resistance. [provided by RefSeq, Jan 2020]","start":116570960,"end":116614820,"strand":-1,"description":"long intergenic non-protein coding RNA 1510 [Source:HGNC Symbol;Acc:HGNC:51196]"}, {"versioned_ensembl_gene_id":"ENSG00000196419.12","gene_symbol":"XRCC6","gene_name":"X-ray repair cross complementing 6 [Source:HGNC Symbol;Acc:HGNC:4055]","synonyms":"D22S731,D22S671,ML8,KU70,G22P1","biotype":"protein_coding","ncbi_id":"2547","summary":"The p70/p80 autoantigen is a nuclear complex consisting of two subunits with molecular masses of approximately 70 and 80 kDa. The complex functions as a single-stranded DNA-dependent ATP-dependent helicase. The complex may be involved in the repair of nonhomologous DNA ends such as that required for double-strand break repair, transposition, and V(D)J recombination. High levels of autoantibodies to p70 and p80 have been found in some patients with systemic lupus erythematosus. [provided by RefSeq, Jul 2008]","start":41621119,"end":41664048,"strand":1,"description":"X-ray repair cross complementing 6 [Source:HGNC Symbol;Acc:HGNC:4055]"}, {"versioned_ensembl_gene_id":"ENSG00000235776.2","gene_symbol":"AC000089.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19792294,"end":19793094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281772.1","gene_symbol":"AC019226.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":148062154,"end":148062577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236979.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31628343,"end":31632433,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000188243.12","gene_symbol":"COMMD6","gene_name":"COMM domain containing 6 [Source:HGNC Symbol;Acc:HGNC:24015]","synonyms":"Acrg","biotype":"protein_coding","ncbi_id":"170622","summary":"COMMD6 belongs to a family of NF-kappa-B (see RELA; MIM 164014)-inhibiting proteins characterized by the presence of a COMM domain (see COMMD1; MIM 607238) (de Bie et al., 2006 [PubMed 16573520]).[supplied by OMIM, Mar 2009]","start":75525219,"end":75549439,"strand":-1,"description":"COMM domain containing 6 [Source:HGNC Symbol;Acc:HGNC:24015]"}, {"versioned_ensembl_gene_id":"ENSG00000258701.1","gene_symbol":"LINC00638","gene_name":"long intergenic non-protein coding RNA 638 [Source:HGNC Symbol;Acc:HGNC:28325]","synonyms":"MGC23270","biotype":"lincRNA","ncbi_id":"196872","summary":null,"start":104821201,"end":104823718,"strand":1,"description":"long intergenic non-protein coding RNA 638 [Source:HGNC Symbol;Acc:HGNC:28325]"}, {"versioned_ensembl_gene_id":"ENSG00000253282.1","gene_symbol":"AP001330.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101287445,"end":101293783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253679.1","gene_symbol":"AP001330.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101261541,"end":101262903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136634.5","gene_symbol":"IL10","gene_name":"interleukin 10 [Source:HGNC Symbol;Acc:HGNC:5962]","synonyms":"IL-10,CSIF,TGIF,IL10A","biotype":"protein_coding","ncbi_id":"3586","summary":"The protein encoded by this gene is a cytokine produced primarily by monocytes and to a lesser extent by lymphocytes. This cytokine has pleiotropic effects in immunoregulation and inflammation. It down-regulates the expression of Th1 cytokines, MHC class II Ags, and costimulatory molecules on macrophages. It also enhances B cell survival, proliferation, and antibody production. This cytokine can block NF-kappa B activity, and is involved in the regulation of the JAK-STAT signaling pathway. Knockout studies in mice suggested the function of this cytokine as an essential immunoregulator in the intestinal tract. Mutations in this gene are associated with an increased susceptibility to HIV-1 infection and rheumatoid arthritis. [provided by RefSeq, May 2020]","start":206767602,"end":206772494,"strand":-1,"description":"interleukin 10 [Source:HGNC Symbol;Acc:HGNC:5962]"}, {"versioned_ensembl_gene_id":"ENSG00000109511.11","gene_symbol":"ANXA10","gene_name":"annexin A10 [Source:HGNC Symbol;Acc:HGNC:534]","synonyms":"ANX14","biotype":"protein_coding","ncbi_id":"11199","summary":"This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. The function of this gene has not yet been determined. [provided by RefSeq, Jul 2008]","start":168092515,"end":168187690,"strand":1,"description":"annexin A10 [Source:HGNC Symbol;Acc:HGNC:534]"}, {"versioned_ensembl_gene_id":"ENSG00000213873.4","gene_symbol":"AC060775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65377592,"end":65378111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134460.15","gene_symbol":"IL2RA","gene_name":"interleukin 2 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6008]","synonyms":"IL2R,IDDM10,CD25","biotype":"protein_coding","ncbi_id":"3559","summary":"The interleukin 2 (IL2) receptor alpha (IL2RA) and beta (IL2RB) chains, together with the common gamma chain (IL2RG), constitute the high-affinity IL2 receptor. Homodimeric alpha chains (IL2RA) result in low-affinity receptor, while homodimeric beta (IL2RB) chains produce a medium-affinity receptor. Normally an integral-membrane protein, soluble IL2RA has been isolated and determined to result from extracellular proteolyisis. Alternately-spliced IL2RA mRNAs have been isolated, but the significance of each is presently unknown. Mutations in this gene are associated with interleukin 2 receptor alpha deficiency. Patients with severe Coronavirus Disease 2019 (COVID-19), the disease caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), have significantly elevated levels of IL2R in their plasma. Similarly, serum IL-2R levels are found to be elevated in patients with different types of carcinomas. Certain IL2RA and IL2RB gene polymorphisms have been associated with lung cancer risk. [provided by RefSeq, Jul 2020]","start":6010689,"end":6062325,"strand":-1,"description":"interleukin 2 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6008]"}, {"versioned_ensembl_gene_id":"ENSG00000248367.1","gene_symbol":"AC008610.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":180293245,"end":180295253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232397.5","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29438848,"end":29440519,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000232525.1","gene_symbol":"SS18L2P1","gene_name":"SS18 like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44965]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646213","summary":null,"start":34875210,"end":34875422,"strand":1,"description":"SS18 like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44965]"}, {"versioned_ensembl_gene_id":"ENSG00000227168.1","gene_symbol":"RPL35AP4","gene_name":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]","synonyms":"BPG294E21.7,OTTHUMG00000140156","biotype":"processed_pseudogene","ncbi_id":"100048922","summary":null,"start":33318189,"end":33318290,"strand":-1,"description":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]"}, {"versioned_ensembl_gene_id":"ENSG00000268560.1","gene_symbol":"AC010636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20611559,"end":20615389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231040.1","gene_symbol":"LINC01911","gene_name":"long intergenic non-protein coding RNA 1911 [Source:HGNC Symbol;Acc:HGNC:52730]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373669","summary":null,"start":146837749,"end":146850310,"strand":1,"description":"long intergenic non-protein coding RNA 1911 [Source:HGNC Symbol;Acc:HGNC:52730]"}, {"versioned_ensembl_gene_id":"ENSG00000004864.13","gene_symbol":"SLC25A13","gene_name":"solute carrier family 25 member 13 [Source:HGNC Symbol;Acc:HGNC:10983]","synonyms":"CTLN2,CITRIN,ARALAR2","biotype":"protein_coding","ncbi_id":"10165","summary":"This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":96120220,"end":96322147,"strand":-1,"description":"solute carrier family 25 member 13 [Source:HGNC Symbol;Acc:HGNC:10983]"}, {"versioned_ensembl_gene_id":"ENSG00000224451.2","gene_symbol":"ATP5F1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422523","summary":null,"start":51598416,"end":51599460,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39742]"}, {"versioned_ensembl_gene_id":"ENSG00000239382.10","gene_symbol":"ALKBH6","gene_name":"alkB homolog 6 [Source:HGNC Symbol;Acc:HGNC:28243]","synonyms":"MGC15677","biotype":"protein_coding","ncbi_id":"84964","summary":null,"start":36009120,"end":36014239,"strand":-1,"description":"alkB homolog 6 [Source:HGNC Symbol;Acc:HGNC:28243]"}, {"versioned_ensembl_gene_id":"ENSG00000254490.1","gene_symbol":"OR5M7P","gene_name":"olfactory receptor family 5 subfamily M member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14818]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79508","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56500300,"end":56501271,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14818]"}, {"versioned_ensembl_gene_id":"ENSG00000124333.15","gene_symbol":"VAMP7","gene_name":"vesicle associated membrane protein 7 [Source:HGNC Symbol;Acc:HGNC:11486]","synonyms":"VAMP-7,TI-VAMP,SYBL1","biotype":"protein_coding","ncbi_id":"6845","summary":"This gene encodes a transmembrane protein that is a member of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) family. The encoded protein localizes to late endosomes and lysosomes and is involved in the fusion of transport vesicles to their target membranes. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]","start":155881293,"end":155943769,"strand":1,"description":"vesicle associated membrane protein 7 [Source:HGNC Symbol;Acc:HGNC:11486]"}, {"versioned_ensembl_gene_id":"ENSG00000225662.2","gene_symbol":"AC012519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62779176,"end":62779785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233844.1","gene_symbol":"KCNQ5-IT1","gene_name":"KCNQ5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41354]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100507381","summary":null,"start":72630495,"end":72678558,"strand":1,"description":"KCNQ5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41354]"}, {"versioned_ensembl_gene_id":"ENSG00000138663.8","gene_symbol":"COPS4","gene_name":"COP9 signalosome subunit 4 [Source:HGNC Symbol;Acc:HGNC:16702]","synonyms":"CSN4","biotype":"protein_coding","ncbi_id":"51138","summary":"This gene encodes one of eight subunits composing COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":83034447,"end":83075818,"strand":1,"description":"COP9 signalosome subunit 4 [Source:HGNC Symbol;Acc:HGNC:16702]"}, {"versioned_ensembl_gene_id":"ENSG00000145808.9","gene_symbol":"ADAMTS19","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 19 [Source:HGNC Symbol;Acc:HGNC:17111]","synonyms":null,"biotype":"protein_coding","ncbi_id":"171019","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene has high sequence similarity to the protein encoded by ADAMTS16, another family member. [provided by RefSeq, Jul 2008]","start":129460265,"end":129738683,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 19 [Source:HGNC Symbol;Acc:HGNC:17111]"}, {"versioned_ensembl_gene_id":"ENSG00000150261.4","gene_symbol":"OR8K1","gene_name":"olfactory receptor family 8 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390157","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56345945,"end":56347031,"strand":1,"description":"olfactory receptor family 8 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14831]"}, {"versioned_ensembl_gene_id":"ENSG00000176198.3","gene_symbol":"OR11H4","gene_name":"olfactory receptor family 11 subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:15347]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390442","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20239286,"end":20244349,"strand":1,"description":"olfactory receptor family 11 subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:15347]"}, {"versioned_ensembl_gene_id":"ENSG00000258806.2","gene_symbol":"OR11H7","gene_name":"olfactory receptor family 11 subfamily H member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15350]","synonyms":"OR11H7P","biotype":"polymorphic_pseudogene","ncbi_id":"390441","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":20229402,"end":20230346,"strand":1,"description":"olfactory receptor family 11 subfamily H member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15350]"}, {"versioned_ensembl_gene_id":"ENSG00000258822.2","gene_symbol":"OR4K16P","gene_name":"olfactory receptor family 4 subfamily K member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:15354]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81126","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19954490,"end":19957996,"strand":1,"description":"olfactory receptor family 4 subfamily K member 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:15354]"}, {"versioned_ensembl_gene_id":"ENSG00000271725.1","gene_symbol":"AC103858.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":81303215,"end":81309391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132693.12","gene_symbol":"CRP","gene_name":"C-reactive protein [Source:HGNC Symbol;Acc:HGNC:2367]","synonyms":"PTX1","biotype":"protein_coding","ncbi_id":"1401","summary":"The protein encoded by this gene belongs to the pentraxin family which also includes serum amyloid P component protein and pentraxin 3. Pentraxins are involved in complement activation and amplification via communication with complement initiation pattern recognition molecules, but also complement regulation via recruitment of complement regulators. The encoded protein has a calcium dependent ligand binding domain with a distinctive flattened beta-jellyroll structure. It exists in two forms as either a pentamer in circulation or as a nonsoluble monomer in tissues. It is involved in several host defense related functions based on its ability to recognize foreign pathogens and damaged cells of the host and to initiate their elimination by interacting with humoral and cellular effector systems in the blood. Consequently, the level of this protein in plasma increases greatly during acute phase response to tissue injury, infection, or other inflammatory stimuli. Elevated expression of the encoded protein is associated with severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection. [provided by RefSeq, Aug 2020]","start":159712289,"end":159714589,"strand":-1,"description":"C-reactive protein [Source:HGNC Symbol;Acc:HGNC:2367]"}, {"versioned_ensembl_gene_id":"ENSG00000284728.1","gene_symbol":"AF228730.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7227853,"end":7228073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258205.1","gene_symbol":"AC079598.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87746567,"end":87746683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154175.16","gene_symbol":"ABI3BP","gene_name":"ABI family member 3 binding protein [Source:HGNC Symbol;Acc:HGNC:17265]","synonyms":"TARSH,NESHBP,DKFZP586L2024","biotype":"protein_coding","ncbi_id":"25890","summary":null,"start":100749156,"end":100993515,"strand":-1,"description":"ABI family member 3 binding protein [Source:HGNC Symbol;Acc:HGNC:17265]"}, {"versioned_ensembl_gene_id":"ENSG00000278399.1","gene_symbol":"AC026120.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56981211,"end":56985960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263083.1","gene_symbol":"AC018630.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":11076769,"end":11079171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262293.1","gene_symbol":"AC242308.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11097196,"end":11097291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214249.3","gene_symbol":"CTAGE11P","gene_name":"CTAGE family member 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:37293]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647288","summary":null,"start":75237944,"end":75240296,"strand":-1,"description":"CTAGE family member 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:37293]"}, {"versioned_ensembl_gene_id":"ENSG00000272718.1","gene_symbol":"AC006518.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10831074,"end":10832016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273092.1","gene_symbol":"TAS2R20","gene_name":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]","synonyms":"TAS2R49,T2R56,T2R20","biotype":"protein_coding","ncbi_id":"259295","summary":"This gene encodes a member of the taste receptor two family of class C G-protein coupled receptors. Receptors of this family have a short extracellular N-terminus, seven transmembrane helices, three extracellular loops and three intracellular loops, and an intracellular C-terminus. Members of this family are expressed in a subset of taste receptor cells, where they function in bitter taste reception, as well as in non-gustatory cells including those of the brain, reproductive organs, respiratory system, and gastrointestinal system. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2016]","start":10996495,"end":10997875,"strand":-1,"description":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]"}, {"versioned_ensembl_gene_id":"ENSG00000235965.2","gene_symbol":"AP000431.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19046310,"end":19047684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275406.1","gene_symbol":"AL359742.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":226331999,"end":226333655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267046.1","gene_symbol":"E2F3P1","gene_name":"E2F transcription factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1872","summary":null,"start":35490009,"end":35491238,"strand":1,"description":"E2F transcription factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3116]"}, {"versioned_ensembl_gene_id":"ENSG00000279912.1","gene_symbol":"AC068448.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32182551,"end":32186475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205045.8","gene_symbol":"SLFN12L","gene_name":"schlafen family member 12 like [Source:HGNC Symbol;Acc:HGNC:33920]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506736","summary":null,"start":35464249,"end":35537861,"strand":-1,"description":"schlafen family member 12 like [Source:HGNC Symbol;Acc:HGNC:33920]"}, {"versioned_ensembl_gene_id":"ENSG00000273144.1","gene_symbol":"TAS2R15P","gene_name":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]","synonyms":"PS8,TAS2R15,T2R15","biotype":"processed_pseudogene","ncbi_id":"266657","summary":null,"start":10964425,"end":10965352,"strand":-1,"description":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]"}, {"versioned_ensembl_gene_id":"ENSG00000174123.10","gene_symbol":"TLR10","gene_name":"toll like receptor 10 [Source:HGNC Symbol;Acc:HGNC:15634]","synonyms":"CD290","biotype":"protein_coding","ncbi_id":"81793","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is most highly expressed in lymphoid tissues such as spleen, lymph node, thymus, and tonsil. Multiple alternatively spliced transcript variants which encode different protein isoforms have been found for this gene. [provided by RefSeq, Aug 2010]","start":38772239,"end":38782990,"strand":-1,"description":"toll like receptor 10 [Source:HGNC Symbol;Acc:HGNC:15634]"}, {"versioned_ensembl_gene_id":"ENSG00000249730.1","gene_symbol":"OR10J4","gene_name":"olfactory receptor family 10 subfamily J member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15408]","synonyms":"OST717,OR10J4P","biotype":"polymorphic_pseudogene","ncbi_id":"391121","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":159432204,"end":159433138,"strand":1,"description":"olfactory receptor family 10 subfamily J member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15408]"}, {"versioned_ensembl_gene_id":"ENSG00000172349.17","gene_symbol":"IL16","gene_name":"interleukin 16 [Source:HGNC Symbol;Acc:HGNC:5980]","synonyms":"prIL-16,LCF,IL-16,HsT19289,FLJ42735,FLJ16806","biotype":"protein_coding","ncbi_id":"3603","summary":"The protein encoded by this gene is a pleiotropic cytokine that functions as a chemoattractant, a modulator of T cell activation, and an inhibitor of HIV replication. The signaling process of this cytokine is mediated by CD4. The product of this gene undergoes proteolytic processing, which is found to yield two functional proteins. The cytokine function is exclusively attributed to the secreted C-terminal peptide, while the N-terminal product may play a role in cell cycle control. Caspase 3 is reported to be involved in the proteolytic processing of this protein. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":81159575,"end":81314058,"strand":1,"description":"interleukin 16 [Source:HGNC Symbol;Acc:HGNC:5980]"}, {"versioned_ensembl_gene_id":"ENSG00000249265.1","gene_symbol":"AC113167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89944910,"end":89947573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248555.6","gene_symbol":"LINC01339","gene_name":"long intergenic non-protein coding RNA 1339 [Source:HGNC Symbol;Acc:HGNC:50549]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101929495","summary":null,"start":90158339,"end":90290071,"strand":-1,"description":"long intergenic non-protein coding RNA 1339 [Source:HGNC Symbol;Acc:HGNC:50549]"}, {"versioned_ensembl_gene_id":"ENSG00000214942.4","gene_symbol":"AC008448.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89900664,"end":89904908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196184.9","gene_symbol":"OR10J1","gene_name":"olfactory receptor family 10 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:8175]","synonyms":"HSHGMP07J,HGMP07J","biotype":"protein_coding","ncbi_id":"26476","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159437845,"end":159443078,"strand":1,"description":"olfactory receptor family 10 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:8175]"}, {"versioned_ensembl_gene_id":"ENSG00000254471.1","gene_symbol":"AP001284.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79987513,"end":79989630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258800.1","gene_symbol":"AL136038.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63598874,"end":63599248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183508.4","gene_symbol":"FAM46C","gene_name":"family with sequence similarity 46 member C [Source:HGNC Symbol;Acc:HGNC:24712]","synonyms":"FLJ20202","biotype":"protein_coding","ncbi_id":"54855","summary":null,"start":117605934,"end":117628372,"strand":1,"description":"family with sequence similarity 46 member C [Source:HGNC Symbol;Acc:HGNC:24712]"}, {"versioned_ensembl_gene_id":"ENSG00000279119.1","gene_symbol":"AC006449.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":38727833,"end":38728198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185883.11","gene_symbol":"ATP6V0C","gene_name":"ATPase H+ transporting V0 subunit c [Source:HGNC Symbol;Acc:HGNC:855]","synonyms":"ATPL,ATP6L,ATP6C,Vma3,VATL","biotype":"protein_coding","ncbi_id":"527","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. This gene encodes the V0 subunit c. Alternative splicing results in transcript variants. Pseudogenes have been identified on chromosomes 6 and 17. [provided by RefSeq, Nov 2010]","start":2513870,"end":2520218,"strand":1,"description":"ATPase H+ transporting V0 subunit c [Source:HGNC Symbol;Acc:HGNC:855]"}, {"versioned_ensembl_gene_id":"ENSG00000267141.1","gene_symbol":"AC012615.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1860250,"end":1862019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235340.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29983944,"end":29984821,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000223352.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29923817,"end":29924002,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000225516.6","gene_symbol":"FAM197Y5","gene_name":"family with sequence similarity 197 Y-linked member 5 [Source:HGNC Symbol;Acc:HGNC:37467]","synonyms":"FAM197Y5P","biotype":"lincRNA","ncbi_id":"100289150","summary":null,"start":9458613,"end":9465974,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 5 [Source:HGNC Symbol;Acc:HGNC:37467]"}, {"versioned_ensembl_gene_id":"ENSG00000217135.2","gene_symbol":"AL590004.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3921847,"end":3922146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241932.1","gene_symbol":"AC092324.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12881170,"end":12881493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074771.3","gene_symbol":"NOX3","gene_name":"NADPH oxidase 3 [Source:HGNC Symbol;Acc:HGNC:7890]","synonyms":"GP91-3","biotype":"protein_coding","ncbi_id":"50508","summary":"This gene encodes a member of the NOX family of NADPH oxidases. These enzymes have the capacity to generate superoxide and other reactive oxygen species (ROS) and transport electrons across the plasma membrane. The ROS generated by family members have been implicated in numerous biological functions including host defense, posttranlational processing of proteins, cellular signaling, regulation of gene expression, and cell differentiation. The protein encoded by this gene is expressed predominantly in the inner ear and is involved in the biogenesis of otoconia/otolith, which are crystalline structures of the inner ear involved in the perception of gravity.[provided by RefSeq, May 2009]","start":155395370,"end":155455903,"strand":-1,"description":"NADPH oxidase 3 [Source:HGNC Symbol;Acc:HGNC:7890]"}, {"versioned_ensembl_gene_id":"ENSG00000178188.14","gene_symbol":"SH2B1","gene_name":"SH2B adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:30417]","synonyms":"SH2B,FLJ30542","biotype":"protein_coding","ncbi_id":"25970","summary":"This gene encodes a member of the SH2-domain containing mediators family. The encoded protein mediates activation of various kinases and may function in cytokine and growth factor receptor signaling and cellular transformation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":28846600,"end":28874212,"strand":1,"description":"SH2B adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:30417]"}, {"versioned_ensembl_gene_id":"ENSG00000282859.1","gene_symbol":"AC003992.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":114560961,"end":114561517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204701.2","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29108059,"end":29114770,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000229228.1","gene_symbol":"LINC00582","gene_name":"long intergenic non-protein coding RNA 582 [Source:HGNC Symbol;Acc:HGNC:43842]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287814","summary":null,"start":231591292,"end":231612090,"strand":-1,"description":"long intergenic non-protein coding RNA 582 [Source:HGNC Symbol;Acc:HGNC:43842]"}, {"versioned_ensembl_gene_id":"ENSG00000260386.6","gene_symbol":"LINC01225","gene_name":"LINC01225 pseudogene [Source:HGNC Symbol;Acc:HGNC:49677]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"149086","summary":null,"start":31500085,"end":31509648,"strand":1,"description":"LINC01225 pseudogene [Source:HGNC Symbol;Acc:HGNC:49677]"}, {"versioned_ensembl_gene_id":"ENSG00000227565.8","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"NFKBIL,IKBL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31586326,"end":31598283,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000224165.5","gene_symbol":"DNAJC27-AS1","gene_name":"DNAJC27 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42943]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729723","summary":null,"start":24971390,"end":25039694,"strand":1,"description":"DNAJC27 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42943]"}, {"versioned_ensembl_gene_id":"ENSG00000274834.1","gene_symbol":"AC010333.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12614451,"end":12614852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228793.1","gene_symbol":"AL138881.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3594247,"end":3624747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235532.1","gene_symbol":"LINC00402","gene_name":"long intergenic non-protein coding RNA 402 [Source:HGNC Symbol;Acc:HGNC:42732]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507612","summary":null,"start":74231457,"end":74259976,"strand":1,"description":"long intergenic non-protein coding RNA 402 [Source:HGNC Symbol;Acc:HGNC:42732]"}, {"versioned_ensembl_gene_id":"ENSG00000223577.2","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bCX101P6.9,bQB115I13.2,bPG299F13.9,FLJ40123","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31276325,"end":31282581,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000187010.19","gene_symbol":"RHD","gene_name":"Rh blood group D antigen [Source:HGNC Symbol;Acc:HGNC:10009]","synonyms":"RhPI,RhII,Rh4,Rh30a,RH,DIIIc,CD240D","biotype":"protein_coding","ncbi_id":"6007","summary":"The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene, which encodes the RhD protein, and a second gene that encodes both the RhC and RhE antigens on a single polypeptide. The two genes, and a third unrelated gene, are found in a cluster on chromosome 1. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":25272393,"end":25330445,"strand":1,"description":"Rh blood group D antigen [Source:HGNC Symbol;Acc:HGNC:10009]"}, {"versioned_ensembl_gene_id":"ENSG00000226303.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29707631,"end":29708053,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000274068.1","gene_symbol":"AL449266.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":108837660,"end":108963484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231522.1","gene_symbol":"AL662848.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30829379,"end":30838017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232441.2","gene_symbol":"CR788250.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32561005,"end":32561100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230366.9","gene_symbol":"DSCR9","gene_name":"Down syndrome critical region 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16301]","synonyms":"NCRNA00038","biotype":"lincRNA","ncbi_id":"257203","summary":null,"start":37208503,"end":37221736,"strand":1,"description":"Down syndrome critical region 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16301]"}, {"versioned_ensembl_gene_id":"ENSG00000224280.1","gene_symbol":"AC005014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16583782,"end":16586757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234689.1","gene_symbol":"LINC00444","gene_name":"long intergenic non-protein coding RNA 444 [Source:HGNC Symbol;Acc:HGNC:42781]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984570","summary":null,"start":47905329,"end":47907357,"strand":-1,"description":"long intergenic non-protein coding RNA 444 [Source:HGNC Symbol;Acc:HGNC:42781]"}, {"versioned_ensembl_gene_id":"ENSG00000228573.1","gene_symbol":"AL138962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47825330,"end":47835956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234169.1","gene_symbol":"LINC01868","gene_name":"long intergenic non-protein coding RNA 1868 [Source:HGNC Symbol;Acc:HGNC:52688]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985924","summary":null,"start":100669892,"end":100676038,"strand":-1,"description":"long intergenic non-protein coding RNA 1868 [Source:HGNC Symbol;Acc:HGNC:52688]"}, {"versioned_ensembl_gene_id":"ENSG00000227259.2","gene_symbol":"HMGN2P22","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39387]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874468","summary":null,"start":100591150,"end":100591324,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39387]"}, {"versioned_ensembl_gene_id":"ENSG00000239315.4","gene_symbol":"RPL19P13","gene_name":"ribosomal protein L19 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36879]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392193","summary":null,"start":11256020,"end":11256602,"strand":1,"description":"ribosomal protein L19 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36879]"}, {"versioned_ensembl_gene_id":"ENSG00000253576.1","gene_symbol":"AF181450.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91975908,"end":91977418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282726.1","gene_symbol":"IGHV4-28","gene_name":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28400","summary":null,"start":106325025,"end":106325531,"strand":-1,"description":"immunoglobulin heavy variable 4-28 [Source:HGNC Symbol;Acc:HGNC:5645]"}, {"versioned_ensembl_gene_id":"ENSG00000241002.1","gene_symbol":"AC017007.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112738672,"end":112739106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240401.8","gene_symbol":"AC012358.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55282350,"end":55346049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224771.1","gene_symbol":"ATP2B2-IT2","gene_name":"ATP2B2 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41310]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874325","summary":null,"start":10626021,"end":10626807,"strand":-1,"description":"ATP2B2 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41310]"}, {"versioned_ensembl_gene_id":"ENSG00000250046.3","gene_symbol":"AC106864.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112693047,"end":112706810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272772.1","gene_symbol":"AC104109.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":134167170,"end":134226071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253171.1","gene_symbol":"AC037450.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87974165,"end":88019113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230726.9","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32515215,"end":32520425,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000276174.1","gene_symbol":"AC087683.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42052705,"end":42053030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220446.2","gene_symbol":"AL121978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5291030,"end":5291388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275815.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRY,KIRZ,KIR15,KIR2DL6","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754998,"end":54767346,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000254556.1","gene_symbol":"AF131215.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11136898,"end":11138607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225845.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTN7,BTN7,HSBLMHC1,BTL-II,HSBLMHC1,BTL-II","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32470120,"end":32483292,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000127249.14","gene_symbol":"ATP13A4","gene_name":"ATPase 13A4 [Source:HGNC Symbol;Acc:HGNC:25422]","synonyms":"FLJ37958,DKFZp761I1011","biotype":"protein_coding","ncbi_id":"84239","summary":null,"start":193402077,"end":193593111,"strand":-1,"description":"ATPase 13A4 [Source:HGNC Symbol;Acc:HGNC:25422]"}, {"versioned_ensembl_gene_id":"ENSG00000214487.3","gene_symbol":"AC092865.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8427640,"end":8428610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127252.5","gene_symbol":"HRASLS","gene_name":"HRAS like suppressor [Source:HGNC Symbol;Acc:HGNC:14922]","synonyms":"HRASLS1,H-REV107","biotype":"protein_coding","ncbi_id":"57110","summary":null,"start":193241125,"end":193277738,"strand":1,"description":"HRAS like suppressor [Source:HGNC Symbol;Acc:HGNC:14922]"}, {"versioned_ensembl_gene_id":"ENSG00000284461.1","gene_symbol":"RABGEF1","gene_name":"RAB guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:17676]","synonyms":"RABEX5,rabex-5,RABEX5,rabex-5","biotype":"protein_coding","ncbi_id":"27342","summary":"RABGEF1 forms a complex with rabaptin-5 (RABPT5; MIM 603616) that is required for endocytic membrane fusion, and it serves as a specific guanine nucleotide exchange factor (GEF) for RAB5 (RAB5A; MIM 179512) (Horiuchi et al., 1997 [PubMed 9323142]).[supplied by OMIM, Mar 2010]","start":66628958,"end":66811459,"strand":1,"description":"RAB guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:17676]"}, {"versioned_ensembl_gene_id":"ENSG00000179918.18","gene_symbol":"SEPHS2","gene_name":"selenophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:19686]","synonyms":"SPS2b,SPS2","biotype":"protein_coding","ncbi_id":"22928","summary":"This gene encodes an enzyme that catalyzes the production of monoselenophosphate (MSP) from selenide and ATP. MSP is the selenium donor required for synthesis of selenocysteine (Sec), which is co-translationally incorporated into selenoproteins at in-frame UGA codons that normally signal translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is itself a selenoprotein containing a Sec residue at its active site, suggesting the existence of an autoregulatory mechanism. It is preferentially expressed in tissues implicated in the synthesis of selenoproteins and in sites of blood cell development. A pseudogene for this locus has been identified on chromosome 5. [provided by RefSeq, May 2017]","start":30443631,"end":30446181,"strand":-1,"description":"selenophosphate synthetase 2 [Source:HGNC Symbol;Acc:HGNC:19686]"}, {"versioned_ensembl_gene_id":"ENSG00000283051.1","gene_symbol":"LINC01668","gene_name":"long intergenic non-protein coding RNA 1668 [Source:HGNC Symbol;Acc:HGNC:52456]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928311","summary":null,"start":42777819,"end":42779994,"strand":-1,"description":"long intergenic non-protein coding RNA 1668 [Source:HGNC Symbol;Acc:HGNC:52456]"}, {"versioned_ensembl_gene_id":"ENSG00000275778.1","gene_symbol":"AC018630.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10845849,"end":11171598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232747.2","gene_symbol":"IGKV1D-35","gene_name":"immunoglobulin kappa variable 1D-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5754]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28895","summary":null,"start":89895502,"end":89895772,"strand":1,"description":"immunoglobulin kappa variable 1D-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5754]"}, {"versioned_ensembl_gene_id":"ENSG00000212127.5","gene_symbol":"TAS2R14","gene_name":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]","synonyms":"TRB1,T2R14","biotype":"protein_coding","ncbi_id":"50840","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10937406,"end":11171573,"strand":-1,"description":"taste 2 receptor member 14 [Source:HGNC Symbol;Acc:HGNC:14920]"}, {"versioned_ensembl_gene_id":"ENSG00000250036.1","gene_symbol":"IGKV1D-37","gene_name":"immunoglobulin kappa variable 1D-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5755]","synonyms":"O4,IGKV1D37","biotype":"IG_V_gene","ncbi_id":"28894","summary":null,"start":89884740,"end":89885216,"strand":1,"description":"immunoglobulin kappa variable 1D-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5755]"}, {"versioned_ensembl_gene_id":"ENSG00000181109.3","gene_symbol":"OR52P1P","gene_name":"olfactory receptor family 52 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15232]","synonyms":"OR52P1","biotype":"unitary_pseudogene","ncbi_id":"81248","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5726502,"end":5727464,"strand":1,"description":"olfactory receptor family 52 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15232]"}, {"versioned_ensembl_gene_id":"ENSG00000138395.14","gene_symbol":"CDK15","gene_name":"cyclin dependent kinase 15 [Source:HGNC Symbol;Acc:HGNC:14434]","synonyms":"PFTAIRE2,ALS2CR7,PFTK2","biotype":"protein_coding","ncbi_id":"65061","summary":null,"start":201790461,"end":201895550,"strand":1,"description":"cyclin dependent kinase 15 [Source:HGNC Symbol;Acc:HGNC:14434]"}, {"versioned_ensembl_gene_id":"ENSG00000135622.12","gene_symbol":"SEMA4F","gene_name":"ssemaphorin 4F [Source:HGNC Symbol;Acc:HGNC:10734]","synonyms":"SEMAW,SEMAM","biotype":"protein_coding","ncbi_id":"10505","summary":"This gene encodes a transmembrane class IV semaphorin family protein, which plays a role in neural development. This gene may be involved in neurogenesis in prostate cancer, the development of neurofibromas, and breast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":74654228,"end":74683853,"strand":1,"description":"ssemaphorin 4F [Source:HGNC Symbol;Acc:HGNC:10734]"}, {"versioned_ensembl_gene_id":"ENSG00000248100.2","gene_symbol":"AC087257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27547050,"end":27552773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254009.1","gene_symbol":"IGKV2D-38","gene_name":"immunoglobulin kappa variable 2D-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5803]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28879","summary":null,"start":89872463,"end":89872702,"strand":1,"description":"immunoglobulin kappa variable 2D-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5803]"}, {"versioned_ensembl_gene_id":"ENSG00000015676.17","gene_symbol":"NUDCD3","gene_name":"NudC domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22208]","synonyms":"NudCL,KIAA1068","biotype":"protein_coding","ncbi_id":"23386","summary":"The product of this gene functions to maintain the stability of dynein intermediate chain. Depletion of this gene product results in aggregation and degradation of dynein intermediate chain, mislocalization of the dynein complex from kinetochores, spindle microtubules, and spindle poles, and loss of gamma-tubulin from spindle poles. The protein localizes to the Golgi apparatus during interphase, and levels of the protein increase after the G1/S transition. [provided by RefSeq, Jul 2008]","start":44379121,"end":44490880,"strand":-1,"description":"NudC domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22208]"}, {"versioned_ensembl_gene_id":"ENSG00000284673.1","gene_symbol":"AC092865.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8396423,"end":8396641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272732.1","gene_symbol":"AC004982.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7550104,"end":7552440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273035.1","gene_symbol":"AC007684.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39323328,"end":39323804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254753.1","gene_symbol":"AC022690.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13844101,"end":13849109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221845.4","gene_symbol":"C7orf65","gene_name":"chromosome 7 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:34432]","synonyms":"FLJ44108","biotype":"lincRNA","ncbi_id":"401335","summary":null,"start":47655244,"end":47661648,"strand":1,"description":"chromosome 7 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:34432]"}, {"versioned_ensembl_gene_id":"ENSG00000236078.1","gene_symbol":"LINC01447","gene_name":"long intergenic non-protein coding RNA 1447 [Source:HGNC Symbol;Acc:HGNC:50783]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929086","summary":null,"start":47621939,"end":47629893,"strand":1,"description":"long intergenic non-protein coding RNA 1447 [Source:HGNC Symbol;Acc:HGNC:50783]"}, {"versioned_ensembl_gene_id":"ENSG00000282198.1","gene_symbol":"AC243657.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":28930704,"end":28930991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281395.1","gene_symbol":"OR2T7","gene_name":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]","synonyms":"OST723,OR2T7P","biotype":"protein_coding","ncbi_id":"81458","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248447273,"end":248448199,"strand":1,"description":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]"}, {"versioned_ensembl_gene_id":"ENSG00000233096.1","gene_symbol":"AC099541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40970541,"end":40971578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234075.1","gene_symbol":"AL353777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47478214,"end":47479010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244441.1","gene_symbol":"AC126182.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120512850,"end":120513188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275140.1","gene_symbol":"AC245389.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148772640,"end":148784594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229162.1","gene_symbol":"AL445471.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24961345,"end":24963097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205409.3","gene_symbol":"OR52E6","gene_name":"olfactory receptor family 52 subfamily E member 6 [Source:HGNC Symbol;Acc:HGNC:15215]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390078","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5840928,"end":5841952,"strand":-1,"description":"olfactory receptor family 52 subfamily E member 6 [Source:HGNC Symbol;Acc:HGNC:15215]"}, {"versioned_ensembl_gene_id":"ENSG00000181017.5","gene_symbol":"OR56B2P","gene_name":"olfactory receptor family 56 subfamily B member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15246]","synonyms":"OR56B2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390073","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5761153,"end":5767465,"strand":1,"description":"olfactory receptor family 56 subfamily B member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15246]"}, {"versioned_ensembl_gene_id":"ENSG00000180988.2","gene_symbol":"OR52N2","gene_name":"olfactory receptor family 52 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15228]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390077","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5820314,"end":5821348,"strand":1,"description":"olfactory receptor family 52 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15228]"}, {"versioned_ensembl_gene_id":"ENSG00000181023.7","gene_symbol":"OR56B1","gene_name":"olfactory receptor family 56 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:15245]","synonyms":"OR56B1P","biotype":"protein_coding","ncbi_id":"387748","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5736448,"end":5738522,"strand":1,"description":"olfactory receptor family 56 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:15245]"}, {"versioned_ensembl_gene_id":"ENSG00000132661.3","gene_symbol":"NXT1","gene_name":"nuclear transport factor 2 like export factor 1 [Source:HGNC Symbol;Acc:HGNC:15913]","synonyms":"P15,MTR2","biotype":"protein_coding","ncbi_id":"29107","summary":"The protein encoded by this gene is located in the nuclear envelope. It has protein similarity to nuclear transport factor 2. This protein functions as a nuclear export factor in both RAN (Ras-related nuclear protein)- and CRM1 (required for chromosome region maintenance)-dependent pathways. It is found to stimulate the export of U1 snRNA in RAN- and CRM1-dependent pathways and the export of tRNA and mRNA in a CRM1-independent pathway. The encoded protein heterodimerizes with Tap protein and may regulate the ability of Tap protein to mediate nuclear mRNA export. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":23350736,"end":23354777,"strand":1,"description":"nuclear transport factor 2 like export factor 1 [Source:HGNC Symbol;Acc:HGNC:15913]"}, {"versioned_ensembl_gene_id":"ENSG00000223498.1","gene_symbol":"AL929302.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16897651,"end":16898521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284748.1","gene_symbol":"AL513220.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":37596126,"end":37607336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251364.6","gene_symbol":"AC107884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7427266,"end":7512515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223359.2","gene_symbol":"CR354545.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32524368,"end":32524463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116199.11","gene_symbol":"FAM20B","gene_name":"FAM20B, glycosaminoglycan xylosylkinase [Source:HGNC Symbol;Acc:HGNC:23017]","synonyms":"KIAA0475,GXK1","biotype":"protein_coding","ncbi_id":"9917","summary":null,"start":179025804,"end":179076562,"strand":1,"description":"FAM20B, glycosaminoglycan xylosylkinase [Source:HGNC Symbol;Acc:HGNC:23017]"}, {"versioned_ensembl_gene_id":"ENSG00000226260.9","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32478466,"end":32483677,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000179083.6","gene_symbol":"FAM133A","gene_name":"family with sequence similarity 133 member A [Source:HGNC Symbol;Acc:HGNC:26748]","synonyms":"RP1-32F7.2,FLJ37659,CT115","biotype":"protein_coding","ncbi_id":"286499","summary":null,"start":93674013,"end":93712274,"strand":1,"description":"family with sequence similarity 133 member A [Source:HGNC Symbol;Acc:HGNC:26748]"}, {"versioned_ensembl_gene_id":"ENSG00000259180.1","gene_symbol":"AC012378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55680385,"end":55681463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184999.11","gene_symbol":"SLC22A10","gene_name":"solute carrier family 22 member 10 [Source:HGNC Symbol;Acc:HGNC:18057]","synonyms":"OAT5,hOAT5","biotype":"protein_coding","ncbi_id":"387775","summary":null,"start":63137867,"end":63369718,"strand":1,"description":"solute carrier family 22 member 10 [Source:HGNC Symbol;Acc:HGNC:18057]"}, {"versioned_ensembl_gene_id":"ENSG00000280754.1","gene_symbol":"AC009286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22455773,"end":22457423,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262139.9","gene_symbol":"ANO4","gene_name":"anoctamin 4 [Source:HGNC Symbol;Acc:HGNC:23837]","synonyms":"FLJ34272,FLJ34221,TMEM16D,FLJ35277","biotype":"protein_coding","ncbi_id":"121601","summary":null,"start":101111599,"end":101128641,"strand":1,"description":"anoctamin 4 [Source:HGNC Symbol;Acc:HGNC:23837]"}, {"versioned_ensembl_gene_id":"ENSG00000278416.1","gene_symbol":"PMS2P2","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9127]","synonyms":"PMS4,PMS2L2","biotype":"unprocessed_pseudogene","ncbi_id":"5380","summary":null,"start":75344015,"end":75359550,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9127]"}, {"versioned_ensembl_gene_id":"ENSG00000183336.8","gene_symbol":"BOLA2","gene_name":"bolA family member 2 [Source:HGNC Symbol;Acc:HGNC:29488]","synonyms":"My016,BOLA2A","biotype":"protein_coding","ncbi_id":"552900","summary":"This gene is located within a region of a segmental duplication on chromosome 16 and is identical to BOLA2B (bolA family member 2B). The product of this gene belongs to a family of proteins that are widely conserved and may be involved in iron maturation. Related pseudogenes are found multiple different chromosomes. Alternative splicing results in multiple transcript variants. Transcripts initiating at this locus may extend into downstream SMG1 pseudogene 6 (SMG1P6) and encode fusion proteins with a C-terminus related to SMG1 phosphatidylinositol 3-kinase-related kinase. A readthrough locus is represented with GeneID:107282092. [provided by RefSeq, Feb 2016]","start":29443056,"end":29454964,"strand":-1,"description":"bolA family member 2 [Source:HGNC Symbol;Acc:HGNC:29488]"}, {"versioned_ensembl_gene_id":"ENSG00000228076.2","gene_symbol":"AL591719.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108766841,"end":108767584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270251.1","gene_symbol":"AL670379.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120986388,"end":120986639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271128.1","gene_symbol":"AC008608.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134081914,"end":134082040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233746.1","gene_symbol":"LINC00656","gene_name":"long intergenic non-protein coding RNA 656 [Source:HGNC Symbol;Acc:HGNC:27304]","synonyms":null,"biotype":"lincRNA","ncbi_id":"200261","summary":null,"start":23125068,"end":23132621,"strand":-1,"description":"long intergenic non-protein coding RNA 656 [Source:HGNC Symbol;Acc:HGNC:27304]"}, {"versioned_ensembl_gene_id":"ENSG00000258308.5","gene_symbol":"AC079907.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101954998,"end":101962390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248896.2","gene_symbol":"AC105001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10729314,"end":10771392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276095.2","gene_symbol":"LINC01663","gene_name":"long intergenic non-protein coding RNA 1663 [Source:HGNC Symbol;Acc:HGNC:52451]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996432","summary":null,"start":18873543,"end":18894407,"strand":-1,"description":"long intergenic non-protein coding RNA 1663 [Source:HGNC Symbol;Acc:HGNC:52451]"}, {"versioned_ensembl_gene_id":"ENSG00000175489.9","gene_symbol":"LRRC25","gene_name":"leucine rich repeat containing 25 [Source:HGNC Symbol;Acc:HGNC:29806]","synonyms":"MAPA,FLJ38116","biotype":"protein_coding","ncbi_id":"126364","summary":null,"start":18391144,"end":18397617,"strand":-1,"description":"leucine rich repeat containing 25 [Source:HGNC Symbol;Acc:HGNC:29806]"}, {"versioned_ensembl_gene_id":"ENSG00000236126.3","gene_symbol":"CT47A3","gene_name":"cancer/testis antigen family 47, member A3 [Source:HGNC Symbol;Acc:HGNC:33284]","synonyms":"CT47.3","biotype":"protein_coding","ncbi_id":"728082","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120972746,"end":120976068,"strand":-1,"description":"cancer/testis antigen family 47, member A3 [Source:HGNC Symbol;Acc:HGNC:33284]"}, {"versioned_ensembl_gene_id":"ENSG00000270771.1","gene_symbol":"AL670379.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120971808,"end":120972059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279212.1","gene_symbol":"AL390961.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":26695091,"end":26697625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227932.2","gene_symbol":"AL390961.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":26664206,"end":26697295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077238.13","gene_symbol":"IL4R","gene_name":"interleukin 4 receptor [Source:HGNC Symbol;Acc:HGNC:6015]","synonyms":"CD124","biotype":"protein_coding","ncbi_id":"3566","summary":"This gene encodes the alpha chain of the interleukin-4 receptor, a type I transmembrane protein that can bind interleukin 4 and interleukin 13 to regulate IgE production. The encoded protein also can bind interleukin 4 to promote differentiation of Th2 cells. A soluble form of the encoded protein can be produced by proteolysis of the membrane-bound protein, and this soluble form can inhibit IL4-mediated cell proliferation and IL5 upregulation by T-cells. Allelic variations in this gene have been associated with atopy, a condition that can manifest itself as allergic rhinitis, sinusitus, asthma, or eczema. Polymorphisms in this gene are also associated with resistance to human immunodeficiency virus type-1 infection. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]","start":27313668,"end":27364778,"strand":1,"description":"interleukin 4 receptor [Source:HGNC Symbol;Acc:HGNC:6015]"}, {"versioned_ensembl_gene_id":"ENSG00000178804.7","gene_symbol":"H1FOO","gene_name":"H1 histone family member O, oocyte specific [Source:HGNC Symbol;Acc:HGNC:18463]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132243","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. The protein encoded is a replication-independent histone that is a member of the histone H1 family. This gene contains introns, unlike most histone genes. The related mouse gene is expressed only in oocytes. [provided by RefSeq, Oct 2015]","start":129543214,"end":129551467,"strand":1,"description":"H1 histone family member O, oocyte specific [Source:HGNC Symbol;Acc:HGNC:18463]"}, {"versioned_ensembl_gene_id":"ENSG00000244381.1","gene_symbol":"AC007849.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169709295,"end":169709765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178636.8","gene_symbol":"AC092656.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":119192773,"end":119212644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214342.2","gene_symbol":"ATP5F1P2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645973","summary":null,"start":94738652,"end":94739411,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39743]"}, {"versioned_ensembl_gene_id":"ENSG00000121381.4","gene_symbol":"TAS2R9","gene_name":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]","synonyms":"TRB6,T2R9","biotype":"protein_coding","ncbi_id":"50835","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10809094,"end":10810168,"strand":-1,"description":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]"}, {"versioned_ensembl_gene_id":"ENSG00000279305.1","gene_symbol":"AC134026.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":154334809,"end":154337047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272142.1","gene_symbol":"AL359643.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5029972,"end":5043449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282391.1","gene_symbol":"AC024940.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31246713,"end":31246958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085760.14","gene_symbol":"MTIF2","gene_name":"mitochondrial translational initiation factor 2 [Source:HGNC Symbol;Acc:HGNC:7441]","synonyms":"IF-2mt","biotype":"protein_coding","ncbi_id":"4528","summary":"During the initiation of protein biosynthesis, initiation factor-2 (IF-2) promotes the binding of the initiator tRNA to the small subunit of the ribosome in a GTP-dependent manner. Prokaryotic IF-2 is a single polypeptide, while eukaryotic cytoplasmic IF-2 (eIF-2) is a trimeric protein. Bovine liver mitochondria contain IF-2(mt), an 85-kD monomeric protein that is equivalent to prokaryotic IF-2. The predicted 727-amino acid human protein contains a 29-amino acid presequence. Human IF-2(mt) shares 32 to 38% amino acid sequence identity with yeast IF-2(mt) and several prokaryotic IF-2s, with the greatest degree of conservation in the G domains of the proteins. [provided by RefSeq, Mar 2016]","start":55236595,"end":55269347,"strand":-1,"description":"mitochondrial translational initiation factor 2 [Source:HGNC Symbol;Acc:HGNC:7441]"}, {"versioned_ensembl_gene_id":"ENSG00000278110.1","gene_symbol":"SUSD2P2","gene_name":"sushi domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35197]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729450","summary":null,"start":18623339,"end":18625289,"strand":-1,"description":"sushi domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35197]"}, {"versioned_ensembl_gene_id":"ENSG00000283072.1","gene_symbol":"AL158175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22685391,"end":22746107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242371.1","gene_symbol":"IGKV1-39","gene_name":"immunoglobulin kappa variable 1-39 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5740]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28930","summary":null,"start":89319625,"end":89320146,"strand":-1,"description":"immunoglobulin kappa variable 1-39 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5740]"}, {"versioned_ensembl_gene_id":"ENSG00000233419.3","gene_symbol":"AL121994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25125053,"end":25125454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010322.15","gene_symbol":"NISCH","gene_name":"nischarin [Source:HGNC Symbol;Acc:HGNC:18006]","synonyms":"KIAA0975,IRAS,I-1","biotype":"protein_coding","ncbi_id":"11188","summary":"This gene encodes a nonadrenergic imidazoline-1 receptor protein that localizes to the cytosol and anchors to the inner layer of the plasma membrane. The orthologous mouse protein has been shown to influence cytoskeletal organization and cell migration by binding to alpha-5-beta-1 integrin. In humans, this protein has been shown to bind to the adapter insulin receptor substrate 4 (IRS4) to mediate translocation of alpha-5 integrin from the cell membrane to endosomes. Expression of this protein was reduced in human breast cancers while its overexpression reduced tumor growth and metastasis; possibly by limiting the expression of alpha-5 integrin. In human cardiac tissue, this gene was found to affect cell growth and death while in neural tissue it affected neuronal growth and differentiation. Alternative splicing results in multiple transcript variants encoding differerent isoforms. Some isoforms lack the expected C-terminal domains of a functional imidazoline receptor. [provided by RefSeq, Jan 2013]","start":52455118,"end":52493071,"strand":1,"description":"nischarin [Source:HGNC Symbol;Acc:HGNC:18006]"}, {"versioned_ensembl_gene_id":"ENSG00000187231.13","gene_symbol":"SESTD1","gene_name":"SEC14 and spectrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18379]","synonyms":"Solo,DKFZp434O0515","biotype":"protein_coding","ncbi_id":"91404","summary":null,"start":179101692,"end":179264790,"strand":-1,"description":"SEC14 and spectrin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18379]"}, {"versioned_ensembl_gene_id":"ENSG00000224071.1","gene_symbol":"AC009474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66820684,"end":66822570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243335.9","gene_symbol":"KCTD7","gene_name":"potassium channel tetramerization domain containing 7 [Source:HGNC Symbol;Acc:HGNC:21957]","synonyms":"FLJ32069,EPM3,CLN14","biotype":"protein_coding","ncbi_id":"154881","summary":"This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]","start":66628767,"end":66649067,"strand":1,"description":"potassium channel tetramerization domain containing 7 [Source:HGNC Symbol;Acc:HGNC:21957]"}, {"versioned_ensembl_gene_id":"ENSG00000229643.1","gene_symbol":"LINC00280","gene_name":"long intergenic non-protein coding RNA 280 [Source:HGNC Symbol;Acc:HGNC:38803]","synonyms":"NCRNA00280","biotype":"lincRNA","ncbi_id":"100873964","summary":null,"start":6357219,"end":6361413,"strand":-1,"description":"long intergenic non-protein coding RNA 280 [Source:HGNC Symbol;Acc:HGNC:38803]"}, {"versioned_ensembl_gene_id":"ENSG00000217482.2","gene_symbol":"HMGB1P17","gene_name":"high mobility group box 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419974","summary":null,"start":135636086,"end":135636713,"strand":-1,"description":"high mobility group box 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39099]"}, {"versioned_ensembl_gene_id":"ENSG00000066322.14","gene_symbol":"ELOVL1","gene_name":"ELOVL fatty acid elongase 1 [Source:HGNC Symbol;Acc:HGNC:14418]","synonyms":"Ssc1","biotype":"protein_coding","ncbi_id":"64834","summary":null,"start":43363397,"end":43368074,"strand":-1,"description":"ELOVL fatty acid elongase 1 [Source:HGNC Symbol;Acc:HGNC:14418]"}, {"versioned_ensembl_gene_id":"ENSG00000105404.10","gene_symbol":"RABAC1","gene_name":"Rab acceptor 1 [Source:HGNC Symbol;Acc:HGNC:9794]","synonyms":"YIP3,PRAF1,PRA1","biotype":"protein_coding","ncbi_id":"10567","summary":null,"start":41956681,"end":41959390,"strand":-1,"description":"Rab acceptor 1 [Source:HGNC Symbol;Acc:HGNC:9794]"}, {"versioned_ensembl_gene_id":"ENSG00000242590.1","gene_symbol":"AL645608.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1055033,"end":1056116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183049.12","gene_symbol":"CAMK1D","gene_name":"calcium/calmodulin dependent protein kinase ID [Source:HGNC Symbol;Acc:HGNC:19341]","synonyms":"CKLiK","biotype":"protein_coding","ncbi_id":"57118","summary":"This gene is a member of the calcium/calmodulin-dependent protein kinase 1 family, a subfamily of the serine/threonine kinases. The encoded protein is a component of the calcium-regulated calmodulin-dependent protein kinase cascade. It has been associated with multiple processes including regulation of granulocyte function, activation of CREB-dependent gene transcription, aldosterone synthesis, differentiation and activation of neutrophil cells, and apoptosis of erythroleukemia cells. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jan 2015]","start":12349482,"end":12835545,"strand":1,"description":"calcium/calmodulin dependent protein kinase ID [Source:HGNC Symbol;Acc:HGNC:19341]"}, {"versioned_ensembl_gene_id":"ENSG00000122824.10","gene_symbol":"NUDT10","gene_name":"nudix hydrolase 10 [Source:HGNC Symbol;Acc:HGNC:17621]","synonyms":"hDIPP3alpha,DIPP3a","biotype":"protein_coding","ncbi_id":"170685","summary":"This gene is a member of the nudix (nucleoside diphosphate linked moiety X)-type motif containing family. The encoded protein is a phosphohydrolase and may regulate the turnover of diphosphoinositol polyphosphates. The turnover of these high-energy diphosphoinositol polyphosphates represents a molecular switching activity with important regulatory consequences. Molecular switching by diphosphoinositol polyphosphates may contribute to the regulation of intracellular trafficking. In some populations putative prostate cancer susceptibility alleles have been identified for this gene. Alternatively spliced transcript variants, which differ only in the 5' UTR, have been found for this gene. [provided by RefSeq, Feb 2015]","start":51332231,"end":51337525,"strand":1,"description":"nudix hydrolase 10 [Source:HGNC Symbol;Acc:HGNC:17621]"}, {"versioned_ensembl_gene_id":"ENSG00000230003.2","gene_symbol":"AL445646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72445754,"end":72445969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235769.8","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31788620,"end":31790096,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000188157.14","gene_symbol":"AGRN","gene_name":"agrin [Source:HGNC Symbol;Acc:HGNC:329]","synonyms":"AGRIN","biotype":"protein_coding","ncbi_id":"375790","summary":"This gene encodes one of several proteins that are critical in the development of the neuromuscular junction (NMJ), as identified in mouse knock-out studies. The encoded protein contains several laminin G, Kazal type serine protease inhibitor, and epidermal growth factor domains. Additional post-translational modifications occur to add glycosaminoglycans and disulfide bonds. In one family with congenital myasthenic syndrome affecting limb-girdle muscles, a mutation in this gene was found. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]","start":1020123,"end":1056118,"strand":1,"description":"agrin [Source:HGNC Symbol;Acc:HGNC:329]"}, {"versioned_ensembl_gene_id":"ENSG00000115474.6","gene_symbol":"KCNJ13","gene_name":"potassium voltage-gated channel subfamily J member 13 [Source:HGNC Symbol;Acc:HGNC:6259]","synonyms":"LCA16,Kir7.1,Kir1.4","biotype":"protein_coding","ncbi_id":"3769","summary":"This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]","start":232766464,"end":232776568,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 13 [Source:HGNC Symbol;Acc:HGNC:6259]"}, {"versioned_ensembl_gene_id":"ENSG00000237828.1","gene_symbol":"PA2G4P1","gene_name":"proliferation-associated 2G4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8551]","synonyms":"PA2G4P","biotype":"processed_pseudogene","ncbi_id":"389884","summary":null,"start":120868611,"end":120869807,"strand":-1,"description":"proliferation-associated 2G4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8551]"}, {"versioned_ensembl_gene_id":"ENSG00000270453.1","gene_symbol":"AC007566.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92442077,"end":92442489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234350.4","gene_symbol":"AC007405.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170723086,"end":170770768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140854.12","gene_symbol":"KATNB1","gene_name":"katanin regulatory subunit B1 [Source:HGNC Symbol;Acc:HGNC:6217]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10300","summary":"Microtubules, polymers of alpha and beta tubulin subunits, form the mitotic spindle of a dividing cell and help to organize membranous organelles during interphase. Katanin is a heterodimer that consists of a 60 kDa ATPase (p60 subunit A 1) and an 80 kDa accessory protein (p80 subunit B 1). The p60 subunit acts to sever and disassemble microtubules, while the p80 subunit targets the enzyme to the centrosome. Katanin is a member of the AAA family of ATPases. [provided by RefSeq, Jul 2008]","start":57735730,"end":57757250,"strand":1,"description":"katanin regulatory subunit B1 [Source:HGNC Symbol;Acc:HGNC:6217]"}, {"versioned_ensembl_gene_id":"ENSG00000259580.1","gene_symbol":"AC023908.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":39770559,"end":39801333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281949.1","gene_symbol":"AC068473.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79708475,"end":79709405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277367.1","gene_symbol":"AL929601.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18889084,"end":18890424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112541.13","gene_symbol":"PDE10A","gene_name":"phosphodiesterase 10A [Source:HGNC Symbol;Acc:HGNC:8772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10846","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase family. It plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. This protein can hydrolyze both cAMP and cGMP to the corresponding nucleoside 5' monophosphate, but has higher affinity for cAMP, and is more efficient with cAMP as substrate. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2011]","start":165327287,"end":165986603,"strand":-1,"description":"phosphodiesterase 10A [Source:HGNC Symbol;Acc:HGNC:8772]"}, {"versioned_ensembl_gene_id":"ENSG00000163885.11","gene_symbol":"CFAP100","gene_name":"cilia and flagella associated protein 100 [Source:HGNC Symbol;Acc:HGNC:26842]","synonyms":"MIA1,FLJ40083,CCDC37","biotype":"protein_coding","ncbi_id":"348807","summary":null,"start":126394939,"end":126436556,"strand":1,"description":"cilia and flagella associated protein 100 [Source:HGNC Symbol;Acc:HGNC:26842]"}, {"versioned_ensembl_gene_id":"ENSG00000223897.1","gene_symbol":"AC069157.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53486144,"end":53486280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234196.2","gene_symbol":"ZBTB12","gene_name":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]","synonyms":"C6orf46,NG35,G10,D6S59E","biotype":"protein_coding","ncbi_id":"221527","summary":null,"start":31976089,"end":31978474,"strand":-1,"description":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]"}, {"versioned_ensembl_gene_id":"ENSG00000168887.10","gene_symbol":"C2orf68","gene_name":"chromosome 2 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:34353]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388969","summary":null,"start":85606654,"end":85612066,"strand":-1,"description":"chromosome 2 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:34353]"}, {"versioned_ensembl_gene_id":"ENSG00000261451.1","gene_symbol":"AC104964.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":10433672,"end":10438312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267313.7","gene_symbol":"KC6","gene_name":"keratoconus gene 6 [Source:NCBI gene;Acc:641516]","synonyms":null,"biotype":"lincRNA","ncbi_id":"641516","summary":null,"start":41465783,"end":41632185,"strand":-1,"description":"keratoconus gene 6 [Source:NCBI gene;Acc:641516]"}, {"versioned_ensembl_gene_id":"ENSG00000277909.4","gene_symbol":"SPC25","gene_name":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]","synonyms":"AD024,SPBC25,MGC22228","biotype":"protein_coding","ncbi_id":"57405","summary":"This gene encodes a protein that may be involved in kinetochore-microtubule interaction and spindle checkpoint activity. [provided by RefSeq, Jul 2008]","start":168834132,"end":168930360,"strand":-1,"description":"SPC25, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:24031]"}, {"versioned_ensembl_gene_id":"ENSG00000227708.1","gene_symbol":"LINC01850","gene_name":"long intergenic non-protein coding RNA 1850 [Source:HGNC Symbol;Acc:HGNC:52666]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985951","summary":null,"start":153337705,"end":153357422,"strand":1,"description":"long intergenic non-protein coding RNA 1850 [Source:HGNC Symbol;Acc:HGNC:52666]"}, {"versioned_ensembl_gene_id":"ENSG00000255763.1","gene_symbol":"MRPS18CP4","gene_name":"mitochondrial ribosomal protein S18C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29745]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"349842","summary":null,"start":14237091,"end":14237321,"strand":1,"description":"mitochondrial ribosomal protein S18C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29745]"}, {"versioned_ensembl_gene_id":"ENSG00000227760.2","gene_symbol":"AC135001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14192002,"end":14192284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159147.17","gene_symbol":"DONSON","gene_name":"downstream neighbor of SON [Source:HGNC Symbol;Acc:HGNC:2993]","synonyms":"DKFZP434M035,C2TA,C21orf60,B17","biotype":"protein_coding","ncbi_id":"29980","summary":"This gene lies downstream of the SON gene and spans 10 kb on chromosome 21. The function of this gene is unknown. [provided by RefSeq, Jul 2008]","start":33559542,"end":33588708,"strand":-1,"description":"downstream neighbor of SON [Source:HGNC Symbol;Acc:HGNC:2993]"}, {"versioned_ensembl_gene_id":"ENSG00000256044.1","gene_symbol":"AC026333.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122749481,"end":122749586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188848.15","gene_symbol":"BEND4","gene_name":"BEN domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23815]","synonyms":"FLJ43965,FLJ35632,CCDC4","biotype":"protein_coding","ncbi_id":"389206","summary":null,"start":42110938,"end":42152878,"strand":-1,"description":"BEN domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23815]"}, {"versioned_ensembl_gene_id":"ENSG00000177888.7","gene_symbol":"ZBTB41","gene_name":"zinc finger and BTB domain containing 41 [Source:HGNC Symbol;Acc:HGNC:24819]","synonyms":"ZNF924,FRBZ1,FLJ36199,DKFZp686C06120","biotype":"protein_coding","ncbi_id":"360023","summary":null,"start":197153680,"end":197200542,"strand":-1,"description":"zinc finger and BTB domain containing 41 [Source:HGNC Symbol;Acc:HGNC:24819]"}, {"versioned_ensembl_gene_id":"ENSG00000267258.1","gene_symbol":"AC008507.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29921182,"end":29921653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144635.8","gene_symbol":"DYNC1LI1","gene_name":"dynein cytoplasmic 1 light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:18745]","synonyms":"DNCLI1","biotype":"protein_coding","ncbi_id":"51143","summary":"The protein encoded by this gene belongs to light intermediate subunit family, whose members are components of the multiprotein cytoplasmic dynein complex, which is involved in intracellular trafficking and chromosome segregation during mitosis. The protein plays a role in moving the spindle assembly checkpoint (SAC) from kinetochores to spindle poles. The protein may also mediate binding to other cargo molecules to facilitate intracellular vesicle trafficking. [provided by RefSeq, Jul 2016]","start":32525971,"end":32570874,"strand":-1,"description":"dynein cytoplasmic 1 light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:18745]"}, {"versioned_ensembl_gene_id":"ENSG00000232320.6","gene_symbol":"AC009299.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161340816,"end":161341326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114654.7","gene_symbol":"EFCC1","gene_name":"EF-hand and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25692]","synonyms":"FLJ12057,CCDC48,C3orf73","biotype":"protein_coding","ncbi_id":"79825","summary":null,"start":129001629,"end":129040742,"strand":1,"description":"EF-hand and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25692]"}, {"versioned_ensembl_gene_id":"ENSG00000187695.8","gene_symbol":"AC112484.1","gene_name":"Uncharacterized protein FLJ43738 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZUG5]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":128909874,"end":128971330,"strand":-1,"description":"Uncharacterized protein FLJ43738 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZUG5]"}, {"versioned_ensembl_gene_id":"ENSG00000188315.7","gene_symbol":"C3orf62","gene_name":"chromosome 3 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:24771]","synonyms":"FLJ43654","biotype":"protein_coding","ncbi_id":"375341","summary":null,"start":49268602,"end":49277909,"strand":-1,"description":"chromosome 3 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:24771]"}, {"versioned_ensembl_gene_id":"ENSG00000151116.16","gene_symbol":"UEVLD","gene_name":"UEV and lactate/malate dehyrogenase domains [Source:HGNC Symbol;Acc:HGNC:30866]","synonyms":"UEV3,Attp","biotype":"protein_coding","ncbi_id":"55293","summary":null,"start":18529609,"end":18588747,"strand":-1,"description":"UEV and lactate/malate dehyrogenase domains [Source:HGNC Symbol;Acc:HGNC:30866]"}, {"versioned_ensembl_gene_id":"ENSG00000245888.6","gene_symbol":"FLJ21408","gene_name":"uncharacterized LOC400512 [Source:NCBI gene;Acc:400512]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"400512","summary":null,"start":27268205,"end":27290492,"strand":1,"description":"uncharacterized LOC400512 [Source:NCBI gene;Acc:400512]"}, {"versioned_ensembl_gene_id":"ENSG00000163879.10","gene_symbol":"DNALI1","gene_name":"dynein axonemal light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:14353]","synonyms":"P28,hp28,dJ423B22.5","biotype":"protein_coding","ncbi_id":"7802","summary":"This gene is the human homolog of the Chlamydomonas inner dynein arm gene, p28. The precise function of this gene is not known, however, it is a potential candidate for immotile cilia syndrome (ICS). Ultrastructural defects of the inner dynein arms are seen in patients with ICS. Immotile mutant strains of Chlamydomonas, a biflagellated algae, exhibit similar defects. [provided by RefSeq, Jul 2008]","start":37556919,"end":37566857,"strand":1,"description":"dynein axonemal light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:14353]"}, {"versioned_ensembl_gene_id":"ENSG00000274825.1","gene_symbol":"AL023803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38955910,"end":38956547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263237.1","gene_symbol":"AC106796.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20385957,"end":20391164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141505.11","gene_symbol":"ASGR1","gene_name":"asialoglycoprotein receptor 1 [Source:HGNC Symbol;Acc:HGNC:742]","synonyms":"CLEC4H1","biotype":"protein_coding","ncbi_id":"432","summary":"This gene encodes a subunit of the asialoglycoprotein receptor. This receptor is a transmembrane protein that plays a critical role in serum glycoprotein homeostasis by mediating the endocytosis and lysosomal degradation of glycoproteins with exposed terminal galactose or N-acetylgalactosamine residues. The asialoglycoprotein receptor may facilitate hepatic infection by multiple viruses including hepatitis B, and is also a target for liver-specific drug delivery. The asialoglycoprotein receptor is a hetero-oligomeric protein composed of major and minor subunits, which are encoded by different genes. The protein encoded by this gene is the more abundant major subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":7173431,"end":7179564,"strand":-1,"description":"asialoglycoprotein receptor 1 [Source:HGNC Symbol;Acc:HGNC:742]"}, {"versioned_ensembl_gene_id":"ENSG00000026103.21","gene_symbol":"FAS","gene_name":"Fas cell surface death receptor [Source:HGNC Symbol;Acc:HGNC:11920]","synonyms":"APT1,APO-1,TNFRSF6,FAS1,CD95","biotype":"protein_coding","ncbi_id":"355","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains a death domain. It has been shown to play a central role in the physiological regulation of programmed cell death, and has been implicated in the pathogenesis of various malignancies and diseases of the immune system. The interaction of this receptor with its ligand allows the formation of a death-inducing signaling complex that includes Fas-associated death domain protein (FADD), caspase 8, and caspase 10. The autoproteolytic processing of the caspases in the complex triggers a downstream caspase cascade, and leads to apoptosis. This receptor has been also shown to activate NF-kappaB, MAPK3/ERK1, and MAPK8/JNK, and is found to be involved in transducing the proliferating signals in normal diploid fibroblast and T cells. Several alternatively spliced transcript variants have been described, some of which are candidates for nonsense-mediated mRNA decay (NMD). The isoforms lacking the transmembrane domain may negatively regulate the apoptosis mediated by the full length isoform. [provided by RefSeq, Mar 2011]","start":88990582,"end":89015785,"strand":1,"description":"Fas cell surface death receptor [Source:HGNC Symbol;Acc:HGNC:11920]"}, {"versioned_ensembl_gene_id":"ENSG00000236493.2","gene_symbol":"EIF2S2P3","gene_name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31664]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283014","summary":null,"start":92668745,"end":92669743,"strand":-1,"description":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31664]"}, {"versioned_ensembl_gene_id":"ENSG00000114656.10","gene_symbol":"KIAA1257","gene_name":"KIAA1257 [Source:HGNC Symbol;Acc:HGNC:29231]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57501","summary":null,"start":128909866,"end":129002690,"strand":-1,"description":"KIAA1257 [Source:HGNC Symbol;Acc:HGNC:29231]"}, {"versioned_ensembl_gene_id":"ENSG00000228054.2","gene_symbol":"RANP5","gene_name":"RAN, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39860]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129428","summary":null,"start":109046828,"end":109047482,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39860]"}, {"versioned_ensembl_gene_id":"ENSG00000241546.1","gene_symbol":"AC092910.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120041190,"end":120041537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163877.10","gene_symbol":"SNIP1","gene_name":"Smad nuclear interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30587]","synonyms":"PML1","biotype":"protein_coding","ncbi_id":"79753","summary":"This gene encodes a protein that contains a coiled-coil motif and C-terminal forkhead-associated (FHA) domain. The encoded protein functions as a transcriptional coactivator that increases c-Myc activity and inhibits transforming growth factor beta (TGF-beta) and nuclear factor kappa-B (NF-kB) signaling. The encoded protein also regulates the stability of cyclin D1 mRNA, and may play a role in cell proliferation and cancer progression. Mutations in this gene are a cause of psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED). [provided by RefSeq, Mar 2012]","start":37534449,"end":37554344,"strand":-1,"description":"Smad nuclear interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30587]"}, {"versioned_ensembl_gene_id":"ENSG00000260750.5","gene_symbol":"AC092720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87492555,"end":87515635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262771.5","gene_symbol":"SSBP1","gene_name":"single stranded DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11317]","synonyms":"SSBP,mtSSB","biotype":"protein_coding","ncbi_id":"6742","summary":"SSBP1 is a housekeeping gene involved in mitochondrial biogenesis (Tiranti et al., 1995 [PubMed 7789991]). It is also a subunit of a single-stranded DNA (ssDNA)-binding complex involved in the maintenance of genome stability (Huang et al., 2009) [PubMed 19683501].[supplied by OMIM, Feb 2010]","start":141744329,"end":141752534,"strand":1,"description":"single stranded DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11317]"}, {"versioned_ensembl_gene_id":"ENSG00000267270.5","gene_symbol":"PARD6G-AS1","gene_name":"PARD6G antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44109]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100130522","summary":null,"start":80147924,"end":80178432,"strand":1,"description":"PARD6G antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44109]"}, {"versioned_ensembl_gene_id":"ENSG00000215177.3","gene_symbol":"IGLV8OR8-1","gene_name":"immunoglobulin lambda variable 8/OR8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5932]","synonyms":"IGLV8/OR8-1","biotype":"IG_V_pseudogene","ncbi_id":"28756","summary":null,"start":47202444,"end":47202897,"strand":-1,"description":"immunoglobulin lambda variable 8/OR8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5932]"}, {"versioned_ensembl_gene_id":"ENSG00000274252.1","gene_symbol":"GGTLC3","gene_name":"gamma-glutamyltransferase light chain 3 [Source:HGNC Symbol;Acc:HGNC:33426]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728226","summary":"Gamma-glutamyltransferase-1 (GGT1; MIM 612346) is a membrane-bound extracellular enzyme that cleaves gamma-glutamyl peptide bonds in glutathione and other peptides and transfers the gamma-glutamyl moiety to acceptors. Autocatalytic cleavage of the GGT1 precursor polypeptide produces a heavy chain and a light chain that associate with each other to form the functional enzyme. Light chain-only GGTs, such as GGTLC3, contain a region corresponding to the GGT1 light chain, but they lack the membrane-anchoring heavy chain region (Heisterkamp et al., 2008 [PubMed 18357469]).[supplied by OMIM, Oct 2008]","start":18516344,"end":18518161,"strand":-1,"description":"gamma-glutamyltransferase light chain 3 [Source:HGNC Symbol;Acc:HGNC:33426]"}, {"versioned_ensembl_gene_id":"ENSG00000077279.18","gene_symbol":"DCX","gene_name":"doublecortin [Source:HGNC Symbol;Acc:HGNC:2714]","synonyms":"XLIS,SCLH,LISX,DC,DBCN","biotype":"protein_coding","ncbi_id":"1641","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, cognitive disability, subcortical band heterotopia (\"double cortex\" syndrome) in females and lissencephaly (\"smooth brain\" syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]","start":111293779,"end":111412429,"strand":-1,"description":"doublecortin [Source:HGNC Symbol;Acc:HGNC:2714]"}, {"versioned_ensembl_gene_id":"ENSG00000185972.5","gene_symbol":"CCIN","gene_name":"calicin [Source:HGNC Symbol;Acc:HGNC:1568]","synonyms":"KBTBD14,BTBD20","biotype":"protein_coding","ncbi_id":"881","summary":"The protein encoded by this gene is a basic protein of the sperm head cytoskeleton. This protein contains kelch repeats and a BTB/POZ domain and is necessary for normal morphology during sperm differentiation. This gene is intronless. [provided by RefSeq, Jul 2008]","start":36169394,"end":36171334,"strand":1,"description":"calicin [Source:HGNC Symbol;Acc:HGNC:1568]"}, {"versioned_ensembl_gene_id":"ENSG00000223820.5","gene_symbol":"CFL1P1","gene_name":"cofilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28560]","synonyms":"MGC35136,CFLP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"142913","summary":null,"start":87817928,"end":87845612,"strand":1,"description":"cofilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28560]"}, {"versioned_ensembl_gene_id":"ENSG00000275060.1","gene_symbol":"PPP1R26P3","gene_name":"protein phosphatase 1 regulatory subunit 26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42017]","synonyms":"KIAA0649P3","biotype":"unprocessed_pseudogene","ncbi_id":"100132173","summary":null,"start":18400407,"end":18404206,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42017]"}, {"versioned_ensembl_gene_id":"ENSG00000177627.9","gene_symbol":"C12orf54","gene_name":"chromosome 12 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:28553]","synonyms":"MGC35033","biotype":"protein_coding","ncbi_id":"121273","summary":null,"start":48482503,"end":48496512,"strand":1,"description":"chromosome 12 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:28553]"}, {"versioned_ensembl_gene_id":"ENSG00000204385.10","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31863192,"end":31879046,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000257002.1","gene_symbol":"AP000438.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62909546,"end":62918361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177873.12","gene_symbol":"ZNF619","gene_name":"zinc finger protein 619 [Source:HGNC Symbol;Acc:HGNC:26910]","synonyms":"FLJ90764","biotype":"protein_coding","ncbi_id":"285267","summary":null,"start":40477113,"end":40490236,"strand":1,"description":"zinc finger protein 619 [Source:HGNC Symbol;Acc:HGNC:26910]"}, {"versioned_ensembl_gene_id":"ENSG00000253803.1","gene_symbol":"AC091163.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46870902,"end":46872045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276563.1","gene_symbol":"AL359075.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178017127,"end":178017343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226545.1","gene_symbol":"AL357552.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8798475,"end":8799506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101442.9","gene_symbol":"ACTR5","gene_name":"ARP5 actin related protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:14671]","synonyms":"INO80M,FLJ12785,Arp5","biotype":"protein_coding","ncbi_id":"79913","summary":null,"start":38748442,"end":38772520,"strand":1,"description":"ARP5 actin related protein 5 homolog [Source:HGNC Symbol;Acc:HGNC:14671]"}, {"versioned_ensembl_gene_id":"ENSG00000223777.1","gene_symbol":"AC092162.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176809426,"end":176809859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168894.9","gene_symbol":"RNF181","gene_name":"ring finger protein 181 [Source:HGNC Symbol;Acc:HGNC:28037]","synonyms":"HSPC238","biotype":"protein_coding","ncbi_id":"51255","summary":"RNF181 binds the integrin alpha-IIb (ITGA2B; MIM 607759)/beta-3 (ITGB3; MIM 173470) complex and has E3 ubiquitin ligase activity (Brophy et al., 2008 [PubMed 18331836]).[supplied by OMIM, Dec 2008]","start":85595725,"end":85597613,"strand":1,"description":"ring finger protein 181 [Source:HGNC Symbol;Acc:HGNC:28037]"}, {"versioned_ensembl_gene_id":"ENSG00000260580.1","gene_symbol":"AC009035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26721874,"end":26729126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205765.8","gene_symbol":"C5orf51","gene_name":"chromosome 5 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:27750]","synonyms":"LOC285636","biotype":"protein_coding","ncbi_id":"285636","summary":null,"start":41904188,"end":41921636,"strand":1,"description":"chromosome 5 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:27750]"}, {"versioned_ensembl_gene_id":"ENSG00000274925.1","gene_symbol":"AC008741.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25257952,"end":25261066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175105.6","gene_symbol":"ZNF654","gene_name":"zinc finger protein 654 [Source:HGNC Symbol;Acc:HGNC:25612]","synonyms":"FLJ21142,FLJ10997","biotype":"protein_coding","ncbi_id":"55279","summary":null,"start":88059274,"end":88144665,"strand":1,"description":"zinc finger protein 654 [Source:HGNC Symbol;Acc:HGNC:25612]"}, {"versioned_ensembl_gene_id":"ENSG00000262785.5","gene_symbol":"PKLR","gene_name":"pyruvate kinase, liver and RBC [Source:HGNC Symbol;Acc:HGNC:9020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5313","summary":"The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":155305243,"end":155316838,"strand":-1,"description":"pyruvate kinase, liver and RBC [Source:HGNC Symbol;Acc:HGNC:9020]"}, {"versioned_ensembl_gene_id":"ENSG00000177697.17","gene_symbol":"CD151","gene_name":"CD151 molecule (Raph blood group) [Source:HGNC Symbol;Acc:HGNC:1630]","synonyms":"TSPAN24,SFA-1,RAPH,PETA-3","biotype":"protein_coding","ncbi_id":"977","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins and other transmembrane 4 superfamily proteins. It is involved in cellular processes including cell adhesion and may regulate integrin trafficking and/or function. This protein enhances cell motility, invasion and metastasis of cancer cells. Multiple alternatively spliced transcript variants that encode the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":832843,"end":839831,"strand":1,"description":"CD151 molecule (Raph blood group) [Source:HGNC Symbol;Acc:HGNC:1630]"}, {"versioned_ensembl_gene_id":"ENSG00000270022.3","gene_symbol":"Z93241.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42615244,"end":42615907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282495.1","gene_symbol":"IGHD1-7","gene_name":"immunoglobulin heavy diversity 1-7 [Source:HGNC Symbol;Acc:HGNC:5486]","synonyms":"IGHD17,DM1","biotype":"IG_D_gene","ncbi_id":"28509","summary":null,"start":105910678,"end":105910694,"strand":-1,"description":"immunoglobulin heavy diversity 1-7 [Source:HGNC Symbol;Acc:HGNC:5486]"}, {"versioned_ensembl_gene_id":"ENSG00000264000.1","gene_symbol":"AP005059.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5567130,"end":5570942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261893.5","gene_symbol":"CLK2","gene_name":"CDC like kinase 2 [Source:HGNC Symbol;Acc:HGNC:2069]","synonyms":"clk2","biotype":"protein_coding","ncbi_id":"1196","summary":"This gene encodes a dual specificity protein kinase that phosphorylates serine/threonine and tyrosine-containing substrates. Activity of this protein regulates serine- and arginine-rich (SR) proteins of the spliceosomal complex, thereby influencing alternative transcript splicing. Chromosomal translocations have been characterized between this locus and the PAFAH1B3 (platelet-activating factor acetylhydrolase 1b, catalytic subunit 3 (29kDa)) gene on chromosome 19, resulting in the production of a fusion protein. Note that this gene is distinct from the TELO2 gene (GeneID:9894), which shares the CLK2 alias, but encodes a protein that is involved in telomere length regulation. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":155278272,"end":155293895,"strand":-1,"description":"CDC like kinase 2 [Source:HGNC Symbol;Acc:HGNC:2069]"}, {"versioned_ensembl_gene_id":"ENSG00000204387.12","gene_symbol":"C6orf48","gene_name":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]","synonyms":"G8,D6S57","biotype":"protein_coding","ncbi_id":"50854","summary":null,"start":31834608,"end":31839766,"strand":1,"description":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]"}, {"versioned_ensembl_gene_id":"ENSG00000279149.1","gene_symbol":"AL356750.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30344672,"end":30347167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228423.2","gene_symbol":"AL357552.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8805860,"end":8807051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225923.1","gene_symbol":"AC092393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96390652,"end":96391393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266114.1","gene_symbol":"AC015908.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10792059,"end":10794985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186364.11","gene_symbol":"NUDT17","gene_name":"nudix hydrolase 17 [Source:HGNC Symbol;Acc:HGNC:26618]","synonyms":"FLJ34433","biotype":"protein_coding","ncbi_id":"200035","summary":null,"start":145845629,"end":145848953,"strand":1,"description":"nudix hydrolase 17 [Source:HGNC Symbol;Acc:HGNC:26618]"}, {"versioned_ensembl_gene_id":"ENSG00000065308.4","gene_symbol":"TRAM2","gene_name":"translocation associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:16855]","synonyms":"KIAA0057","biotype":"protein_coding","ncbi_id":"9697","summary":"TRAM2 is a component of the translocon, a gated macromolecular channel that controls the posttranslational processing of nascent secretory and membrane proteins at the endoplasmic reticulum (ER) membrane.[supplied by OMIM, Jul 2004]","start":52497402,"end":52576915,"strand":-1,"description":"translocation associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:16855]"}, {"versioned_ensembl_gene_id":"ENSG00000261433.1","gene_symbol":"AC002347.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10658542,"end":10659082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235577.2","gene_symbol":"CR759837.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32460410,"end":32460505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117400.16","gene_symbol":"MPL","gene_name":"MPL proto-oncogene, thrombopoietin receptor [Source:HGNC Symbol;Acc:HGNC:7217]","synonyms":"TPOR,CD110","biotype":"protein_coding","ncbi_id":"4352","summary":"In 1990 an oncogene, v-mpl, was identified from the murine myeloproliferative leukemia virus that was capable of immortalizing bone marrow hematopoietic cells from different lineages. In 1992 the human homologue, named, c-mpl, was cloned. Sequence data revealed that c-mpl encoded a protein that was homologous with members of the hematopoietic receptor superfamily. Presence of anti-sense oligodeoxynucleotides of c-mpl inhibited megakaryocyte colony formation. The ligand for c-mpl, thrombopoietin, was cloned in 1994. Thrombopoietin was shown to be the major regulator of megakaryocytopoiesis and platelet formation. The protein encoded by the c-mpl gene, CD110, is a 635 amino acid transmembrane domain, with two extracellular cytokine receptor domains and two intracellular cytokine receptor box motifs . TPO-R deficient mice were severely thrombocytopenic, emphasizing the important role of CD110 and thrombopoietin in megakaryocyte and platelet formation. Upon binding of thrombopoietin CD110 is dimerized and the JAK family of non-receptor tyrosine kinases, as well as the STAT family, the MAPK family, the adaptor protein Shc and the receptors themselves become tyrosine phosphorylated. [provided by RefSeq, Jul 2008]","start":43337849,"end":43352772,"strand":1,"description":"MPL proto-oncogene, thrombopoietin receptor [Source:HGNC Symbol;Acc:HGNC:7217]"}, {"versioned_ensembl_gene_id":"ENSG00000182308.6","gene_symbol":"DCAF4L1","gene_name":"DDB1 and CUL4 associated factor 4 like 1 [Source:HGNC Symbol;Acc:HGNC:27723]","synonyms":"WDR21B","biotype":"protein_coding","ncbi_id":"285429","summary":null,"start":41981696,"end":41986467,"strand":1,"description":"DDB1 and CUL4 associated factor 4 like 1 [Source:HGNC Symbol;Acc:HGNC:27723]"}, {"versioned_ensembl_gene_id":"ENSG00000233956.1","gene_symbol":"BTF3P6","gene_name":"basic transcription factor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499261","summary":null,"start":33518610,"end":33519108,"strand":-1,"description":"basic transcription factor 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23765]"}, {"versioned_ensembl_gene_id":"ENSG00000180438.15","gene_symbol":"TPRXL","gene_name":"tetrapeptide repeat homeobox like [Source:HGNC Symbol;Acc:HGNC:32178]","synonyms":"TPRX3P,FLJ35107","biotype":"transcribed_processed_pseudogene","ncbi_id":"348825","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the TPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":13937273,"end":14082811,"strand":1,"description":"tetrapeptide repeat homeobox like [Source:HGNC Symbol;Acc:HGNC:32178]"}, {"versioned_ensembl_gene_id":"ENSG00000272485.1","gene_symbol":"AL392183.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":774747,"end":780214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267146.1","gene_symbol":"AC012301.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56872668,"end":56873970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272463.1","gene_symbol":"AL357054.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":708592,"end":711405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007174.17","gene_symbol":"DNAH9","gene_name":"dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]","synonyms":"KIAA0357,HL20,HL-20,DYH9,DNAL1,Dnahc9,DNAH17L","biotype":"protein_coding","ncbi_id":"1770","summary":"This gene encodes the heavy chain subunit of axonemal dynein, a large multi-subunit molecular motor. Axonemal dynein attaches to microtubules and hydrolyzes ATP to mediate the movement of cilia and flagella. The gene expresses at least two transcript variants; additional variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":11598431,"end":11969748,"strand":1,"description":"dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]"}, {"versioned_ensembl_gene_id":"ENSG00000185278.15","gene_symbol":"ZBTB37","gene_name":"zinc finger and BTB domain containing 37 [Source:HGNC Symbol;Acc:HGNC:28365]","synonyms":"ZNF908,MGC2629","biotype":"protein_coding","ncbi_id":"84614","summary":null,"start":173868082,"end":173903549,"strand":1,"description":"zinc finger and BTB domain containing 37 [Source:HGNC Symbol;Acc:HGNC:28365]"}, {"versioned_ensembl_gene_id":"ENSG00000278693.3","gene_symbol":"ASB2","gene_name":"ankyrin repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:16012]","synonyms":"ASB-2","biotype":"protein_coding","ncbi_id":"51676","summary":"This gene encodes a member of the ankyrin repeat and SOCS box-containing (ASB) protein family. These proteins play a role in protein degradation by coupling suppressor of cytokine signalling (SOCS) proteins with the elongin BC complex. The encoded protein is a subunit of a multimeric E3 ubiquitin ligase complex that mediates the degradation of actin-binding proteins. This gene plays a role in retinoic acid-induced growth inhibition and differentiation of myeloid leukemia cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":93934153,"end":93976791,"strand":-1,"description":"ankyrin repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:16012]"}, {"versioned_ensembl_gene_id":"ENSG00000267202.5","gene_symbol":"AC090386.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37273706,"end":37276572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276427.1","gene_symbol":"IGLL4P","gene_name":"immunoglobulin lambda like polypeptide 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:38475]","synonyms":"IGLL4","biotype":"unprocessed_pseudogene","ncbi_id":"100287528","summary":null,"start":20632619,"end":20632751,"strand":1,"description":"immunoglobulin lambda like polypeptide 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:38475]"}, {"versioned_ensembl_gene_id":"ENSG00000234830.7","gene_symbol":"FAM197Y9","gene_name":"family with sequence similarity 197 Y-linked member 9 [Source:HGNC Symbol;Acc:HGNC:37477]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132932","summary":null,"start":6256267,"end":6263953,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 9 [Source:HGNC Symbol;Acc:HGNC:37477]"}, {"versioned_ensembl_gene_id":"ENSG00000216316.1","gene_symbol":"AL022722.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119269133,"end":119269714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280626.1","gene_symbol":"AC226496.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68696372,"end":68697104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237138.1","gene_symbol":"HUNK-AS1","gene_name":"HUNK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40631]","synonyms":"TCONS_00028914","biotype":"antisense_RNA","ncbi_id":"106144524","summary":null,"start":32020966,"end":32021782,"strand":-1,"description":"HUNK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40631]"}, {"versioned_ensembl_gene_id":"ENSG00000271870.1","gene_symbol":"AC024060.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3152942,"end":3153435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204257.14","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32948613,"end":32969094,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000282445.1","gene_symbol":"AC243757.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16016803,"end":16017400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249726.1","gene_symbol":"TUBB1P1","gene_name":"tubulin beta 1 class VI pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23982]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"349448","summary":null,"start":18386974,"end":18389151,"strand":1,"description":"tubulin beta 1 class VI pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23982]"}, {"versioned_ensembl_gene_id":"ENSG00000233645.1","gene_symbol":"AL358876.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8218190,"end":8220529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233522.1","gene_symbol":"FAM224A","gene_name":"family with sequence similarity 224 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37736]","synonyms":"NCRNA00230A,LINC00230A","biotype":"lincRNA","ncbi_id":"401630","summary":"This locus is transcribed but does not appear to encode a protein. Two identical copies of this gene are present in a palindromic region on chromosome Y. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":18326253,"end":18353210,"strand":1,"description":"family with sequence similarity 224 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37736]"}, {"versioned_ensembl_gene_id":"ENSG00000281095.1","gene_symbol":"AC233263.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90309230,"end":90309333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237917.1","gene_symbol":"PARP4P1","gene_name":"poly(ADP-ribose) polymerase family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18500]","synonyms":"PARP4PY1,PARP4P,ADPRTL1P","biotype":"unprocessed_pseudogene","ncbi_id":"347613","summary":null,"start":26594851,"end":26634652,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18500]"}, {"versioned_ensembl_gene_id":"ENSG00000114166.7","gene_symbol":"KAT2B","gene_name":"lysine acetyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:8638]","synonyms":"PCAF,P/CAF,GCN5L,GCN5","biotype":"protein_coding","ncbi_id":"8850","summary":"CBP and p300 are large nuclear proteins that bind to many sequence-specific factors involved in cell growth and/or differentiation, including c-jun and the adenoviral oncoprotein E1A. The protein encoded by this gene associates with p300/CBP. It has in vitro and in vivo binding activity with CBP and p300, and competes with E1A for binding sites in p300/CBP. It has histone acetyl transferase activity with core histones and nucleosome core particles, indicating that this protein plays a direct role in transcriptional regulation. [provided by RefSeq, Jul 2008]","start":20040023,"end":20154404,"strand":1,"description":"lysine acetyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:8638]"}, {"versioned_ensembl_gene_id":"ENSG00000277283.1","gene_symbol":"AC004812.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120116907,"end":120119000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229358.3","gene_symbol":"DPY19L1P1","gene_name":"DPY19L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22395]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129460","summary":null,"start":32580949,"end":32761787,"strand":-1,"description":"DPY19L1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22395]"}, {"versioned_ensembl_gene_id":"ENSG00000234893.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ25550,Em:AB014087.1,FLJ31598","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30280294,"end":30316632,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000280350.1","gene_symbol":"LINC01726","gene_name":"long intergenic non-protein coding RNA 1726 [Source:HGNC Symbol;Acc:HGNC:52514]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929608","summary":null,"start":21610787,"end":21703585,"strand":-1,"description":"long intergenic non-protein coding RNA 1726 [Source:HGNC Symbol;Acc:HGNC:52514]"}, {"versioned_ensembl_gene_id":"ENSG00000235123.5","gene_symbol":"DSCAM-AS1","gene_name":"DSCAM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40197]","synonyms":"M41","biotype":"antisense_RNA","ncbi_id":"100506492","summary":null,"start":40383083,"end":40385358,"strand":1,"description":"DSCAM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40197]"}, {"versioned_ensembl_gene_id":"ENSG00000282105.1","gene_symbol":"RPL41P2","gene_name":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"22970","summary":null,"start":28428588,"end":28428996,"strand":1,"description":"ribosomal protein L41 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10357]"}, {"versioned_ensembl_gene_id":"ENSG00000236683.3","gene_symbol":"HMGA1P1","gene_name":"high mobility group AT-hook 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13321]","synonyms":"HMGIYL1,HMGA1L1","biotype":"processed_pseudogene","ncbi_id":"203477","summary":null,"start":26748029,"end":26749090,"strand":1,"description":"high mobility group AT-hook 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13321]"}, {"versioned_ensembl_gene_id":"ENSG00000232326.9","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"ABCB3,PSF2,D6S217E,RING11","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32912700,"end":32929495,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000213484.2","gene_symbol":"EIF4A1P8","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289102","summary":null,"start":92136875,"end":92138370,"strand":1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37927]"}, {"versioned_ensembl_gene_id":"ENSG00000120160.10","gene_symbol":"EQTN","gene_name":"equatorin [Source:HGNC Symbol;Acc:HGNC:1359]","synonyms":"equatorin,C9orf11,AFAF,SPACA8","biotype":"protein_coding","ncbi_id":"54586","summary":null,"start":27284659,"end":27297139,"strand":-1,"description":"equatorin [Source:HGNC Symbol;Acc:HGNC:1359]"}, {"versioned_ensembl_gene_id":"ENSG00000130385.5","gene_symbol":"BMP15","gene_name":"bone morphogenetic protein 15 [Source:HGNC Symbol;Acc:HGNC:1068]","synonyms":"GDF9B","biotype":"protein_coding","ncbi_id":"9210","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate subunits of a disulfide-linked homodimer, or alternatively, a heterodimer, with the related protein, growth differentiation factor 9 (GDF9). This protein plays a role in oocyte maturation and follicular development, through activation of granulosa cells. Defects in this gene are the cause of ovarian dysgenesis and are associated with premature ovarian failure. [provided by RefSeq, Aug 2016]","start":50910784,"end":50916607,"strand":1,"description":"bone morphogenetic protein 15 [Source:HGNC Symbol;Acc:HGNC:1068]"}, {"versioned_ensembl_gene_id":"ENSG00000146926.10","gene_symbol":"ASB10","gene_name":"ankyrin repeat and SOCS box containing 10 [Source:HGNC Symbol;Acc:HGNC:17185]","synonyms":"GLC1F","biotype":"protein_coding","ncbi_id":"136371","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. The SOCS box serves to couple suppressor of cytokine signaling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2008]","start":151175698,"end":151187832,"strand":-1,"description":"ankyrin repeat and SOCS box containing 10 [Source:HGNC Symbol;Acc:HGNC:17185]"}, {"versioned_ensembl_gene_id":"ENSG00000267425.1","gene_symbol":"LINC01928","gene_name":"long intergenic non-protein coding RNA 1928 [Source:HGNC Symbol;Acc:HGNC:52750]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371994","summary":null,"start":11454478,"end":11465996,"strand":1,"description":"long intergenic non-protein coding RNA 1928 [Source:HGNC Symbol;Acc:HGNC:52750]"}, {"versioned_ensembl_gene_id":"ENSG00000267252.5","gene_symbol":"LINC01255","gene_name":"long intergenic non-protein coding RNA 1255 [Source:HGNC Symbol;Acc:HGNC:49871]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927433","summary":null,"start":11488570,"end":11506983,"strand":1,"description":"long intergenic non-protein coding RNA 1255 [Source:HGNC Symbol;Acc:HGNC:49871]"}, {"versioned_ensembl_gene_id":"ENSG00000282412.1","gene_symbol":"AC243629.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15970173,"end":15971302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255680.1","gene_symbol":"AC091564.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6618790,"end":6619764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230956.2","gene_symbol":"AL024493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88096393,"end":88097225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185596.16","gene_symbol":"WASH3P","gene_name":"WAS protein family homolog 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:24362]","synonyms":"FLJ25222,FAM39DP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"374666","summary":null,"start":101961603,"end":101976543,"strand":1,"description":"WAS protein family homolog 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:24362]"}, {"versioned_ensembl_gene_id":"ENSG00000081803.15","gene_symbol":"CADPS2","gene_name":"calcium dependent secretion activator 2 [Source:HGNC Symbol;Acc:HGNC:16018]","synonyms":"CAPS2","biotype":"protein_coding","ncbi_id":"93664","summary":"This gene encodes a member of the calcium-dependent activator of secretion (CAPS) protein family, which are calcium binding proteins that regulate the exocytosis of synaptic and dense-core vesicles in neurons and neuroendocrine cells. Mutations in this gene may contribute to autism susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2009]","start":122318425,"end":122886759,"strand":-1,"description":"calcium dependent secretion activator 2 [Source:HGNC Symbol;Acc:HGNC:16018]"}, {"versioned_ensembl_gene_id":"ENSG00000105171.9","gene_symbol":"POP4","gene_name":"POP4 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:30081]","synonyms":"RPP29","biotype":"protein_coding","ncbi_id":"10775","summary":"This gene encodes one of the protein subunits of the small nucleolar ribonucleoprotein complexes: the endoribonuclease for mitochondrial RNA processing complex and the ribonuclease P complex. The encoded protein is localized to the nucleus and associates directly with the RNA component of these complexes. This protein is involved in processing of precursor RNAs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":29604017,"end":29617237,"strand":1,"description":"POP4 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:30081]"}, {"versioned_ensembl_gene_id":"ENSG00000196504.15","gene_symbol":"PRPF40A","gene_name":"pre-mRNA processing factor 40 homolog A [Source:HGNC Symbol;Acc:HGNC:16463]","synonyms":"Prp40,NY-REN-6,HYPA,HIP10,FNBP3,FLJ20585,FLAF1,FBP11,FBP-11","biotype":"protein_coding","ncbi_id":"55660","summary":null,"start":152651593,"end":152717997,"strand":-1,"description":"pre-mRNA processing factor 40 homolog A [Source:HGNC Symbol;Acc:HGNC:16463]"}, {"versioned_ensembl_gene_id":"ENSG00000213866.3","gene_symbol":"YBX1P10","gene_name":"Y-box binding protein 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42432]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158373","summary":null,"start":35971344,"end":35972318,"strand":-1,"description":"Y-box binding protein 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42432]"}, {"versioned_ensembl_gene_id":"ENSG00000162496.8","gene_symbol":"DHRS3","gene_name":"dehydrogenase/reductase 3 [Source:HGNC Symbol;Acc:HGNC:17693]","synonyms":"SDR16C1,SDR1,Rsdr1,retSDR1,RDH17","biotype":"protein_coding","ncbi_id":"9249","summary":"Short-chain dehydrogenases/reductases (SDRs), such as DHRS3, catalyze the oxidation/reduction of a wide range of substrates, including retinoids and steroids (Haeseleer and Palczewski, 2000 [PubMed 10800688]).[supplied by OMIM, Jun 2009]","start":12567910,"end":12617731,"strand":-1,"description":"dehydrogenase/reductase 3 [Source:HGNC Symbol;Acc:HGNC:17693]"}, {"versioned_ensembl_gene_id":"ENSG00000259616.2","gene_symbol":"AC104574.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61298791,"end":61635449,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177693.3","gene_symbol":"OR4F4","gene_name":"olfactory receptor family 4 subfamily F member 4 [Source:HGNC Symbol;Acc:HGNC:8301]","synonyms":"OR4F18","biotype":"protein_coding","ncbi_id":"26682","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101922042,"end":101923095,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 4 [Source:HGNC Symbol;Acc:HGNC:8301]"}, {"versioned_ensembl_gene_id":"ENSG00000232848.1","gene_symbol":"AL034417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8057245,"end":8058463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255519.1","gene_symbol":"AC103855.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45514187,"end":45514451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158352.15","gene_symbol":"SHROOM4","gene_name":"shroom family member 4 [Source:HGNC Symbol;Acc:HGNC:29215]","synonyms":"KIAA1202","biotype":"protein_coding","ncbi_id":"57477","summary":"This gene encodes a member of the APX/Shroom family, which contain an N-terminal PDZ domain and a C-terminal ASD2 motif. The encoded protein may play a role in cytoskeletal architecture. Mutations in this gene have been linked to the X-linked Stocco dos Santos syndrome characterized by cognitive disabilities. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2017]","start":50591647,"end":50814302,"strand":-1,"description":"shroom family member 4 [Source:HGNC Symbol;Acc:HGNC:29215]"}, {"versioned_ensembl_gene_id":"ENSG00000259635.1","gene_symbol":"AC100830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64701248,"end":64719602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237775.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bQB10J12.1,bPG70P20.2,TIGD1L,bCX111D4.7","biotype":"antisense_RNA","ncbi_id":"414771","summary":null,"start":30866982,"end":30875918,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000116285.12","gene_symbol":"ERRFI1","gene_name":"ERBB receptor feedback inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:18185]","synonyms":"RALT,MIG-6,GENE-33","biotype":"protein_coding","ncbi_id":"54206","summary":"ERRFI1 is a cytoplasmic protein whose expression is upregulated with cell growth (Wick et al., 1995 [PubMed 7641805]). It shares significant homology with the protein product of rat gene-33, which is induced during cell stress and mediates cell signaling (Makkinje et al., 2000 [PubMed 10749885]; Fiorentino et al., 2000 [PubMed 11003669]).[supplied by OMIM, Mar 2008]","start":8004404,"end":8026308,"strand":-1,"description":"ERBB receptor feedback inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:18185]"}, {"versioned_ensembl_gene_id":"ENSG00000274036.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54824676,"end":54838980,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000229310.1","gene_symbol":"RPP40P1","gene_name":"ribonuclease P/MRP subunit p40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39769]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874225","summary":null,"start":25591353,"end":25591808,"strand":-1,"description":"ribonuclease P/MRP subunit p40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39769]"}, {"versioned_ensembl_gene_id":"ENSG00000228519.3","gene_symbol":"AC097263.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25645722,"end":25646327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176812.7","gene_symbol":"AC112778.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25194381,"end":25195207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164099.3","gene_symbol":"PRSS12","gene_name":"protease, serine 12 [Source:HGNC Symbol;Acc:HGNC:9477]","synonyms":"MRT1,BSSP-3","biotype":"protein_coding","ncbi_id":"8492","summary":"This gene encodes a member of the trypsin family of serine proteases and contains a signal peptide, a proline-rich region, a Kringle domain, four scavenger receptor cysteine-rich domains, and a trypsin-like serine protease domain. The protein, sometimes referred to as neurotrypsin or motopsin, is secreted from neuronal cells and localizes to the synaptic cleft. Studies in mice show that this protein cleaves a protein, agrin, that is important for the formation and maintenance of exitatory synapses. Defects in this gene cause a form of autosomal recessive cognitive impairment (MRT1). [provided by RefSeq, Jul 2017]","start":118280038,"end":118353003,"strand":-1,"description":"protease, serine 12 [Source:HGNC Symbol;Acc:HGNC:9477]"}, {"versioned_ensembl_gene_id":"ENSG00000281617.2","gene_symbol":"ANKRD18DP","gene_name":"ankyrin repeat domain 18D, pseudogene [Source:HGNC Symbol;Acc:HGNC:28016]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"348840","summary":null,"start":198053522,"end":198080720,"strand":-1,"description":"ankyrin repeat domain 18D, pseudogene [Source:HGNC Symbol;Acc:HGNC:28016]"}, {"versioned_ensembl_gene_id":"ENSG00000241671.1","gene_symbol":"AC117394.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153129074,"end":153129640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185627.17","gene_symbol":"PSMD13","gene_name":"proteasome 26S subunit, non-ATPase 13 [Source:HGNC Symbol;Acc:HGNC:9558]","synonyms":"Rpn9,p40.5","biotype":"protein_coding","ncbi_id":"5719","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. Two transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":236546,"end":252984,"strand":1,"description":"proteasome 26S subunit, non-ATPase 13 [Source:HGNC Symbol;Acc:HGNC:9558]"}, {"versioned_ensembl_gene_id":"ENSG00000184494.8","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31848038,"end":31853285,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000266505.1","gene_symbol":"AL354674.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30022021,"end":30023800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267284.1","gene_symbol":"AC022031.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55721063,"end":55788761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255164.1","gene_symbol":"AF235103.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144992914,"end":144994837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250202.2","gene_symbol":"AC093827.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86876338,"end":86876652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274843.3","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195719081,"end":195738792,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000128645.14","gene_symbol":"HOXD1","gene_name":"homeobox D1 [Source:HGNC Symbol;Acc:HGNC:5132]","synonyms":"HOX4G,HOX4","biotype":"protein_coding","ncbi_id":"3231","summary":"This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis. [provided by RefSeq, Jul 2008]","start":176188579,"end":176190907,"strand":1,"description":"homeobox D1 [Source:HGNC Symbol;Acc:HGNC:5132]"}, {"versioned_ensembl_gene_id":"ENSG00000231083.1","gene_symbol":"AC011747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8600892,"end":8622942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184140.6","gene_symbol":"OR4F6","gene_name":"olfactory receptor family 4 subfamily F member 6 [Source:HGNC Symbol;Acc:HGNC:15372]","synonyms":"OR4F12","biotype":"protein_coding","ncbi_id":"390648","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101803509,"end":101806887,"strand":1,"description":"olfactory receptor family 4 subfamily F member 6 [Source:HGNC Symbol;Acc:HGNC:15372]"}, {"versioned_ensembl_gene_id":"ENSG00000188996.4","gene_symbol":"HUS1B","gene_name":"HUS1 checkpoint clamp component B [Source:HGNC Symbol;Acc:HGNC:16485]","synonyms":null,"biotype":"protein_coding","ncbi_id":"135458","summary":"The protein encoded by this gene is most closely related to HUS1, a component of a cell cycle checkpoint protein complex involved in cell cycle arrest in response to DNA damage. This protein can interact with the check point protein RAD1 but not with RAD9. Overexpression of this protein has been shown to induce cell death, which suggests a related but distinct role of this protein, as compared to the HUS1. [provided by RefSeq, Jul 2008]","start":655939,"end":656963,"strand":-1,"description":"HUS1 checkpoint clamp component B [Source:HGNC Symbol;Acc:HGNC:16485]"}, {"versioned_ensembl_gene_id":"ENSG00000237919.5","gene_symbol":"AL158840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70013982,"end":70031222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004468.12","gene_symbol":"CD38","gene_name":"CD38 molecule [Source:HGNC Symbol;Acc:HGNC:1667]","synonyms":null,"biotype":"protein_coding","ncbi_id":"952","summary":"The protein encoded by this gene is a non-lineage-restricted, type II transmembrane glycoprotein that synthesizes and hydrolyzes cyclic adenosine 5'-diphosphate-ribose, an intracellular calcium ion mobilizing messenger. The release of soluble protein and the ability of membrane-bound protein to become internalized indicate both extracellular and intracellular functions for the protein. This protein has an N-terminal cytoplasmic tail, a single membrane-spanning domain, and a C-terminal extracellular region with four N-glycosylation sites. Crystal structure analysis demonstrates that the functional molecule is a dimer, with the central portion containing the catalytic site. It is used as a prognostic marker for patients with chronic lymphocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":15778275,"end":15853230,"strand":1,"description":"CD38 molecule [Source:HGNC Symbol;Acc:HGNC:1667]"}, {"versioned_ensembl_gene_id":"ENSG00000229359.2","gene_symbol":"PIN1P1","gene_name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8989]","synonyms":"PIN1L","biotype":"transcribed_processed_pseudogene","ncbi_id":"5301","summary":null,"start":69919322,"end":69920317,"strand":1,"description":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8989]"}, {"versioned_ensembl_gene_id":"ENSG00000169402.15","gene_symbol":"RSPH10B2","gene_name":"radial spoke head 10 homolog B2 [Source:HGNC Symbol;Acc:HGNC:34385]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728194","summary":"This gene encodes a protein component of the radial spoke head in flagella and motile cilia. Eukaryotic flagella and motile cilia share a common 9 + 2 structure, in which nine peripheral microtubule doublets (MTDs) surround a central-pair of microtubules (CP), with radial spokes connecting the MTDs to the CP. The radial spoke is a multi-protein complex that works as a mechanochemical transducer between the CP and the MTDs. The radial spoke contributes to the regulation of the activity of dynein motors, and thus to flagellar motility. PMID: 22754630 provides a good review of radial spokes. [provided by RefSeq, Jul 2017]","start":6754109,"end":6799365,"strand":1,"description":"radial spoke head 10 homolog B2 [Source:HGNC Symbol;Acc:HGNC:34385]"}, {"versioned_ensembl_gene_id":"ENSG00000167608.11","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160108,"end":54173250,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000276392.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5.1,KIR2DL5,KIR2DL5,CD158F,KIR2DL5.1,CD158F","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819505,"end":54829001,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000234888.1","gene_symbol":"OFD1P15Y","gene_name":"OFD1 pseudogene 15, Y-linked [Source:HGNC Symbol;Acc:HGNC:23887]","synonyms":"OFDYP15,OFD1PY15,OFD1P15","biotype":"unprocessed_pseudogene","ncbi_id":"386699","summary":null,"start":26055779,"end":26088493,"strand":-1,"description":"OFD1 pseudogene 15, Y-linked [Source:HGNC Symbol;Acc:HGNC:23887]"}, {"versioned_ensembl_gene_id":"ENSG00000233052.1","gene_symbol":"AL513304.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1361001,"end":1361637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230433.1","gene_symbol":"AL031770.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":524171,"end":525581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224969.1","gene_symbol":"AL645608.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1011997,"end":1013193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178498.15","gene_symbol":"DTX3","gene_name":"deltex E3 ubiquitin ligase 3 [Source:HGNC Symbol;Acc:HGNC:24457]","synonyms":"RNF154,FLJ34766","biotype":"protein_coding","ncbi_id":"196403","summary":"DTX3 functions as an E3 ubiquitin ligase (Takeyama et al., 2003 [PubMed 12670957]).[supplied by OMIM, Nov 2009]","start":57604622,"end":57609804,"strand":1,"description":"deltex E3 ubiquitin ligase 3 [Source:HGNC Symbol;Acc:HGNC:24457]"}, {"versioned_ensembl_gene_id":"ENSG00000174749.5","gene_symbol":"C4orf32","gene_name":"chromosome 4 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26813]","synonyms":"FLJ39370","biotype":"protein_coding","ncbi_id":"132720","summary":null,"start":112145397,"end":112195256,"strand":1,"description":"chromosome 4 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:26813]"}, {"versioned_ensembl_gene_id":"ENSG00000225855.6","gene_symbol":"RUSC1-AS1","gene_name":"RUSC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26680]","synonyms":"FLJ35976,C1orf104","biotype":"antisense_RNA","ncbi_id":"284618","summary":null,"start":155316863,"end":155324176,"strand":-1,"description":"RUSC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26680]"}, {"versioned_ensembl_gene_id":"ENSG00000265545.1","gene_symbol":"AP005403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4459230,"end":4459458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198146.4","gene_symbol":"ZNF770","gene_name":"zinc finger protein 770 [Source:HGNC Symbol;Acc:HGNC:26061]","synonyms":"PRO1914,FLJ20582","biotype":"protein_coding","ncbi_id":"54989","summary":null,"start":34978341,"end":34988287,"strand":-1,"description":"zinc finger protein 770 [Source:HGNC Symbol;Acc:HGNC:26061]"}, {"versioned_ensembl_gene_id":"ENSG00000001631.15","gene_symbol":"KRIT1","gene_name":"KRIT1, ankyrin repeat containing [Source:HGNC Symbol;Acc:HGNC:1573]","synonyms":"CAM,CCM1","biotype":"protein_coding","ncbi_id":"889","summary":"This gene encodes a protein containing four ankyrin repeats, a band 4.1/ezrin/radixin/moesin (FERM) domain, and multiple NPXY sequences. The encoded protein is localized in the nucleus and cytoplasm. It binds to integrin cytoplasmic domain-associated protein-1 alpha (ICAP1alpha), and plays a critical role in beta1-integrin-mediated cell proliferation. It associates with junction proteins and RAS-related protein 1A (Rap1A), which requires the encoded protein for maintaining the integrity of endothelial junctions. It is also a microtubule-associated protein and may play a role in microtubule targeting. Mutations in this gene result in cerebral cavernous malformations. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":92198969,"end":92246166,"strand":-1,"description":"KRIT1, ankyrin repeat containing [Source:HGNC Symbol;Acc:HGNC:1573]"}, {"versioned_ensembl_gene_id":"ENSG00000215440.11","gene_symbol":"NPEPL1","gene_name":"aminopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:16244]","synonyms":"FLJ11583,bA261P9.2","biotype":"protein_coding","ncbi_id":"79716","summary":null,"start":58689131,"end":58719238,"strand":1,"description":"aminopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:16244]"}, {"versioned_ensembl_gene_id":"ENSG00000185818.7","gene_symbol":"NAT8L","gene_name":"N-acetyltransferase 8 like [Source:HGNC Symbol;Acc:HGNC:26742]","synonyms":"Hcml3,FLJ37478","biotype":"protein_coding","ncbi_id":"339983","summary":"This gene encodes a single-pass membrane protein, which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily. This protein is a neuron-specific protein and is the N-acetylaspartate (NAA) biosynthetic enzyme, catalyzing the NAA synthesis from L-aspartate and acetyl-CoA. NAA is a major storage and transport form of acetyl coenzyme A specific to the nervous system. The gene mutation results in primary NAA deficiency (hypoacetylaspartia). [provided by RefSeq, Dec 2010]","start":2059512,"end":2069089,"strand":1,"description":"N-acetyltransferase 8 like [Source:HGNC Symbol;Acc:HGNC:26742]"}, {"versioned_ensembl_gene_id":"ENSG00000276463.4","gene_symbol":"TAF9","gene_name":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]","synonyms":"MGC3647,MGC1603,CGI-137,TAFIID32,AD-004,TAFII32,TAFII31,TAF2G,MGC5067","biotype":"protein_coding","ncbi_id":"6880","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the smaller subunits of TFIID that binds to the basal transcription factor GTF2B as well as to several transcriptional activators such as p53 and VP16. In human, TAF9 and AK6 (GeneID: 102157402) are two distinct genes that share 5' exons. A similar but distinct gene (TAF9L) has been found on the X chromosome and a pseudogene has been identified on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":69364756,"end":69370027,"strand":-1,"description":"TATA-box binding protein associated factor 9 [Source:HGNC Symbol;Acc:HGNC:11542]"}, {"versioned_ensembl_gene_id":"ENSG00000178821.12","gene_symbol":"TMEM52","gene_name":"transmembrane protein 52 [Source:HGNC Symbol;Acc:HGNC:27916]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339456","summary":null,"start":1917590,"end":1919273,"strand":-1,"description":"transmembrane protein 52 [Source:HGNC Symbol;Acc:HGNC:27916]"}, {"versioned_ensembl_gene_id":"ENSG00000185610.6","gene_symbol":"DBX2","gene_name":"developing brain homeobox 2 [Source:HGNC Symbol;Acc:HGNC:33186]","synonyms":"FLJ16139","biotype":"protein_coding","ncbi_id":"440097","summary":null,"start":45014672,"end":45051099,"strand":-1,"description":"developing brain homeobox 2 [Source:HGNC Symbol;Acc:HGNC:33186]"}, {"versioned_ensembl_gene_id":"ENSG00000225256.1","gene_symbol":"TRAPPC2P5","gene_name":"trafficking protein particle complex 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:10714]","synonyms":"SEDLP5","biotype":"unprocessed_pseudogene","ncbi_id":"27193","summary":null,"start":25699451,"end":25702562,"strand":1,"description":"trafficking protein particle complex 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:10714]"}, {"versioned_ensembl_gene_id":"ENSG00000274310.1","gene_symbol":"AC091076.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54467208,"end":54470609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267320.5","gene_symbol":"AC005580.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28316705,"end":28386204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241810.1","gene_symbol":"HMGN2P13","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:33557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289682","summary":null,"start":153067278,"end":153067551,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:33557]"}, {"versioned_ensembl_gene_id":"ENSG00000150471.16","gene_symbol":"ADGRL3","gene_name":"adhesion G protein-coupled receptor L3 [Source:HGNC Symbol;Acc:HGNC:20974]","synonyms":"LPHN3,LEC3,KIAA0768","biotype":"protein_coding","ncbi_id":"23284","summary":"This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/calcitonin family of GPCRs) being non-covalently bound at the cell membrane. [provided by RefSeq, Jul 2008]","start":61201258,"end":62078335,"strand":1,"description":"adhesion G protein-coupled receptor L3 [Source:HGNC Symbol;Acc:HGNC:20974]"}, {"versioned_ensembl_gene_id":"ENSG00000261061.1","gene_symbol":"AC092718.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":81030770,"end":81031485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169347.16","gene_symbol":"GP2","gene_name":"glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:4441]","synonyms":"ZAP75","biotype":"protein_coding","ncbi_id":"2813","summary":"This gene encodes an integral membrane protein that is secreted from intracellular zymogen granules and associates with the plasma membrane via glycosylphosphatidylinositol (GPI) linkage. The encoded protein binds pathogens such as enterobacteria, thereby playing an important role in the innate immune response. The C-terminus of this protein is related to the C-terminus of the protein encoded by the neighboring gene, uromodulin (UMOD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":20309572,"end":20327808,"strand":-1,"description":"glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:4441]"}, {"versioned_ensembl_gene_id":"ENSG00000244005.12","gene_symbol":"NFS1","gene_name":"NFS1, cysteine desulfurase [Source:HGNC Symbol;Acc:HGNC:15910]","synonyms":"NifS,IscS","biotype":"protein_coding","ncbi_id":"9054","summary":"Iron-sulfur clusters are required for the function of many cellular enzymes. The proteins encoded by this gene supply inorganic sulfur to these clusters by removing the sulfur from cysteine, creating alanine in the process. This gene uses alternate in-frame translation initiation sites to generate mitochondrial forms and cytoplasmic/nuclear forms. Selection of the alternative initiation sites is determined by the cytosolic pH. The encoded proteins belong to the class-V family of pyridoxal phosphate-dependent aminotransferases. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]","start":35668055,"end":35699359,"strand":-1,"description":"NFS1, cysteine desulfurase [Source:HGNC Symbol;Acc:HGNC:15910]"}, {"versioned_ensembl_gene_id":"ENSG00000276428.1","gene_symbol":"AC245505.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22066016,"end":22066373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101746.15","gene_symbol":"NOL4","gene_name":"nucleolar protein 4 [Source:HGNC Symbol;Acc:HGNC:7870]","synonyms":"NOLP,HRIHFB2255,CT125","biotype":"protein_coding","ncbi_id":"8715","summary":null,"start":33851100,"end":34224952,"strand":-1,"description":"nucleolar protein 4 [Source:HGNC Symbol;Acc:HGNC:7870]"}, {"versioned_ensembl_gene_id":"ENSG00000267746.1","gene_symbol":"AC104985.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34222965,"end":34224761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263105.1","gene_symbol":"AC009171.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4180117,"end":4183515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152049.6","gene_symbol":"KCNE4","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:6244]","synonyms":"MiRP3","biotype":"protein_coding","ncbi_id":"23704","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the embryo and in adult uterus. [provided by RefSeq, Jul 2008]","start":223051814,"end":223198399,"strand":1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:6244]"}, {"versioned_ensembl_gene_id":"ENSG00000278021.4","gene_symbol":"PRAMEF8","gene_name":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391002","summary":null,"start":13299884,"end":13303717,"strand":-1,"description":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]"}, {"versioned_ensembl_gene_id":"ENSG00000277022.1","gene_symbol":"AL031663.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45435272,"end":45448325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278943.1","gene_symbol":"AC079228.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145376909,"end":145377957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253887.1","gene_symbol":"AC022784.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9255349,"end":9260295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274360.2","gene_symbol":"OR6W1P","gene_name":"olfactory receptor family 6 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15091]","synonyms":"sdolf,OR6W1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"89883","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143123517,"end":143124772,"strand":-1,"description":"olfactory receptor family 6 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15091]"}, {"versioned_ensembl_gene_id":"ENSG00000260034.1","gene_symbol":"LCMT1-AS2","gene_name":"LCMT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51178]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506655","summary":null,"start":25140577,"end":25149032,"strand":-1,"description":"LCMT1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51178]"}, {"versioned_ensembl_gene_id":"ENSG00000277378.1","gene_symbol":"OR6V1","gene_name":"olfactory receptor family 6 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15090]","synonyms":"GPR138","biotype":"protein_coding","ncbi_id":"346517","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143113507,"end":143114534,"strand":1,"description":"olfactory receptor family 6 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15090]"}, {"versioned_ensembl_gene_id":"ENSG00000277974.5","gene_symbol":"TBC1D3H","gene_name":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729877","summary":null,"start":36377903,"end":36388795,"strand":-1,"description":"TBC1 domain family member 3H [Source:HGNC Symbol;Acc:HGNC:30708]"}, {"versioned_ensembl_gene_id":"ENSG00000276299.5","gene_symbol":"PRAMEF25","gene_name":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441873","summary":null,"start":13169610,"end":13178799,"strand":-1,"description":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]"}, {"versioned_ensembl_gene_id":"ENSG00000088970.15","gene_symbol":"KIZ","gene_name":"kizuna centrosomal protein [Source:HGNC Symbol;Acc:HGNC:15865]","synonyms":"NCRNA00153,HT013,C20orf19,PLK1S1","biotype":"protein_coding","ncbi_id":"55857","summary":"The protein encoded by this gene localizes to centrosomes, strengthening and stabilizing the pericentriolar region prior to spindle formation. The encoded protein usually remains with the mother centrosome after centrosomal duplication. Sevral transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":21125983,"end":21246622,"strand":1,"description":"kizuna centrosomal protein [Source:HGNC Symbol;Acc:HGNC:15865]"}, {"versioned_ensembl_gene_id":"ENSG00000263270.5","gene_symbol":"AC093689.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34657606,"end":34669432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237090.1","gene_symbol":"AL512353.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42891094,"end":42892430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233708.1","gene_symbol":"AL512353.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42886597,"end":42888767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273914.2","gene_symbol":"OR9A2","gene_name":"olfactory receptor family 9 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15093]","synonyms":null,"biotype":"protein_coding","ncbi_id":"135924","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143087345,"end":143088382,"strand":-1,"description":"olfactory receptor family 9 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15093]"}, {"versioned_ensembl_gene_id":"ENSG00000236878.1","gene_symbol":"MTATP6P26","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:52182]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075301","summary":null,"start":120211054,"end":120211715,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:52182]"}, {"versioned_ensembl_gene_id":"ENSG00000277075.2","gene_symbol":"HIST1H2AE","gene_name":"histone cluster 1 H2A family member e [Source:HGNC Symbol;Acc:HGNC:4724]","synonyms":"H2AFA,H2A/a,H2A.1","biotype":"protein_coding","ncbi_id":"3012","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26216975,"end":26217483,"strand":1,"description":"histone cluster 1 H2A family member e [Source:HGNC Symbol;Acc:HGNC:4724]"}, {"versioned_ensembl_gene_id":"ENSG00000257999.1","gene_symbol":"AC016257.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105102472,"end":105107179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237862.1","gene_symbol":"Z94160.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37352190,"end":37354839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280877.1","gene_symbol":"FABP5P13","gene_name":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]","synonyms":"FABP5L13","biotype":"processed_pseudogene","ncbi_id":"106480712","summary":null,"start":522755,"end":523082,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]"}, {"versioned_ensembl_gene_id":"ENSG00000254999.3","gene_symbol":"BRK1","gene_name":"BRICK1, SCAR/WAVE actin nucleating complex subunit [Source:HGNC Symbol;Acc:HGNC:23057]","synonyms":"MDS027,HSPC300,C3orf10","biotype":"protein_coding","ncbi_id":"55845","summary":null,"start":10115592,"end":10127190,"strand":1,"description":"BRICK1, SCAR/WAVE actin nucleating complex subunit [Source:HGNC Symbol;Acc:HGNC:23057]"}, {"versioned_ensembl_gene_id":"ENSG00000105376.4","gene_symbol":"ICAM5","gene_name":"intercellular adhesion molecule 5 [Source:HGNC Symbol;Acc:HGNC:5348]","synonyms":"TLN,TLCN","biotype":"protein_coding","ncbi_id":"7087","summary":"The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein is expressed on the surface of telencephalic neurons and displays two types of adhesion activity, homophilic binding between neurons and heterophilic binding between neurons and leukocytes. It may be a critical component in neuron-microglial cell interactions in the course of normal development or as part of neurodegenerative diseases. [provided by RefSeq, Jul 2008]","start":10289981,"end":10296778,"strand":1,"description":"intercellular adhesion molecule 5 [Source:HGNC Symbol;Acc:HGNC:5348]"}, {"versioned_ensembl_gene_id":"ENSG00000130590.13","gene_symbol":"SAMD10","gene_name":"sterile alpha motif domain containing 10 [Source:HGNC Symbol;Acc:HGNC:16129]","synonyms":"C20orf136","biotype":"protein_coding","ncbi_id":"140700","summary":null,"start":63974113,"end":63980008,"strand":-1,"description":"sterile alpha motif domain containing 10 [Source:HGNC Symbol;Acc:HGNC:16129]"}, {"versioned_ensembl_gene_id":"ENSG00000236594.2","gene_symbol":"RPS27AP14","gene_name":"ribosomal protein S27a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36530]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271378","summary":null,"start":1164414,"end":1164867,"strand":-1,"description":"ribosomal protein S27a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36530]"}, {"versioned_ensembl_gene_id":"ENSG00000268112.1","gene_symbol":"AC008761.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17727840,"end":17734513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213613.2","gene_symbol":"RPL11P3","gene_name":"ribosomal protein L11 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271271","summary":null,"start":87945502,"end":87946024,"strand":1,"description":"ribosomal protein L11 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36342]"}, {"versioned_ensembl_gene_id":"ENSG00000237412.6","gene_symbol":"PRSS56","gene_name":"protease, serine 56 [Source:HGNC Symbol;Acc:HGNC:39433]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646960","summary":"This gene encodes a protein that contains a peptidase S1 domain and possesses trypsin-like serine protease activity. The encoded protein may play a role in eye development, and mutations in this gene are a cause of autosomal recessive posterior microphthalmos. [provided by RefSeq, Dec 2011]","start":232520463,"end":232525716,"strand":1,"description":"protease, serine 56 [Source:HGNC Symbol;Acc:HGNC:39433]"}, {"versioned_ensembl_gene_id":"ENSG00000231441.1","gene_symbol":"AL512422.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56844002,"end":56864078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248618.1","gene_symbol":"ENPP7P3","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481658","summary":null,"start":130167790,"end":130168030,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48686]"}, {"versioned_ensembl_gene_id":"ENSG00000279695.1","gene_symbol":"AL359757.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25141536,"end":25141809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237834.9","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTN6,BTNL11","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29653572,"end":29668964,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000151846.8","gene_symbol":"PABPC3","gene_name":"poly(A) binding protein cytoplasmic 3 [Source:HGNC Symbol;Acc:HGNC:8556]","synonyms":"tPABP,PABPL3,PABP3","biotype":"protein_coding","ncbi_id":"5042","summary":"Messenger RNA stability and translation initiation are extensively under the control of poly(A)-binding proteins (PABP). See PABPC1 (MIM 604679) for background information.[supplied by OMIM, Jul 2002]","start":25095868,"end":25099254,"strand":1,"description":"poly(A) binding protein cytoplasmic 3 [Source:HGNC Symbol;Acc:HGNC:8556]"}, {"versioned_ensembl_gene_id":"ENSG00000276958.1","gene_symbol":"AL590099.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25017766,"end":25017903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225330.1","gene_symbol":"AF064860.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":39630271,"end":39726085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272693.3","gene_symbol":"AC073107.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65647010,"end":65770810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231144.1","gene_symbol":"EEF1A1P40","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:37918]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874490","summary":null,"start":107032248,"end":107032820,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:37918]"}, {"versioned_ensembl_gene_id":"ENSG00000242268.2","gene_symbol":"LINC02082","gene_name":"long intergenic non-protein coding RNA 2082 [Source:HGNC Symbol;Acc:HGNC:52931]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507661","summary":null,"start":168903366,"end":168921996,"strand":1,"description":"long intergenic non-protein coding RNA 2082 [Source:HGNC Symbol;Acc:HGNC:52931]"}, {"versioned_ensembl_gene_id":"ENSG00000227888.4","gene_symbol":"FAM66A","gene_name":"family with sequence similarity 66 member A [Source:HGNC Symbol;Acc:HGNC:30444]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133172","summary":null,"start":12362019,"end":12388296,"strand":1,"description":"family with sequence similarity 66 member A [Source:HGNC Symbol;Acc:HGNC:30444]"}, {"versioned_ensembl_gene_id":"ENSG00000149480.6","gene_symbol":"MTA2","gene_name":"metastasis associated 1 family member 2 [Source:HGNC Symbol;Acc:HGNC:7411]","synonyms":"MTA1L1,MTA1-L1","biotype":"protein_coding","ncbi_id":"9219","summary":"This gene encodes a protein that has been identified as a component of NuRD, a nucleosome remodeling deacetylase complex identified in the nucleus of human cells. It shows a very broad expression pattern and is strongly expressed in many tissues. It may represent one member of a small gene family that encode different but related proteins involved either directly or indirectly in transcriptional regulation. Their indirect effects on transcriptional regulation may include chromatin remodeling. It is closely related to another member of this family, a protein that has been correlated with the metastatic potential of certain carcinomas. These two proteins are so closely related that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. One of the proteins known to be a target protein for this gene product is p53. Deacetylation of p53 is correlated with a loss of growth inhibition in transformed cells supporting a connection between these gene family members and metastasis. [provided by RefSeq, May 2011]","start":62593214,"end":62601840,"strand":-1,"description":"metastasis associated 1 family member 2 [Source:HGNC Symbol;Acc:HGNC:7411]"}, {"versioned_ensembl_gene_id":"ENSG00000226754.1","gene_symbol":"AL606760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53238610,"end":53242783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264311.1","gene_symbol":"CCDC58P1","gene_name":"coiled-coil domain containing 58 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645859","summary":null,"start":10623876,"end":10624305,"strand":-1,"description":"coiled-coil domain containing 58 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32457]"}, {"versioned_ensembl_gene_id":"ENSG00000272259.5","gene_symbol":"LINC01749","gene_name":"long intergenic non-protein coding RNA 1749 [Source:HGNC Symbol;Acc:HGNC:52537]","synonyms":null,"biotype":"lincRNA","ncbi_id":"63930","summary":null,"start":63009383,"end":63085071,"strand":1,"description":"long intergenic non-protein coding RNA 1749 [Source:HGNC Symbol;Acc:HGNC:52537]"}, {"versioned_ensembl_gene_id":"ENSG00000177981.10","gene_symbol":"ASB8","gene_name":"ankyrin repeat and SOCS box containing 8 [Source:HGNC Symbol;Acc:HGNC:17183]","synonyms":"MGC5540,FLJ21255","biotype":"protein_coding","ncbi_id":"140461","summary":null,"start":48147788,"end":48181213,"strand":-1,"description":"ankyrin repeat and SOCS box containing 8 [Source:HGNC Symbol;Acc:HGNC:17183]"}, {"versioned_ensembl_gene_id":"ENSG00000155100.10","gene_symbol":"OTUD6B","gene_name":"OTU domain containing 6B [Source:HGNC Symbol;Acc:HGNC:24281]","synonyms":"DUBA5,CGI-77","biotype":"protein_coding","ncbi_id":"51633","summary":"This gene encodes a member of the ovarian tumor domain (OTU)-containing subfamily of deubiquitinating enzymes. Deubiquitinating enzymes are primarily involved in removing ubiquitin from proteins targeted for degradation. This protein may function as a negative regulator of the cell cycle in B cells. [provided by RefSeq, Nov 2013]","start":91070196,"end":91087095,"strand":1,"description":"OTU domain containing 6B [Source:HGNC Symbol;Acc:HGNC:24281]"}, {"versioned_ensembl_gene_id":"ENSG00000224547.1","gene_symbol":"ZNF619P1","gene_name":"zinc finger protein 619 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419776","summary":null,"start":46144937,"end":46145688,"strand":1,"description":"zinc finger protein 619 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50784]"}, {"versioned_ensembl_gene_id":"ENSG00000007341.18","gene_symbol":"ST7L","gene_name":"suppression of tumorigenicity 7 like [Source:HGNC Symbol;Acc:HGNC:18441]","synonyms":"STLR,ST7R,FLJ20284,FAM4B","biotype":"protein_coding","ncbi_id":"54879","summary":"This gene was identified by its similarity to the ST7 tumor suppressor gene found in the chromosome 7q31 region. This gene is clustered in a tail-to-tail manner with the WNT2B gene in a chromosomal region known to be deleted and rearranged in a variety of cancers. Several transcript variants encoding many different isoforms have been described, but some have not been fully characterized. [provided by RefSeq, Feb 2011]","start":112523518,"end":112620825,"strand":-1,"description":"suppression of tumorigenicity 7 like [Source:HGNC Symbol;Acc:HGNC:18441]"}, {"versioned_ensembl_gene_id":"ENSG00000010295.19","gene_symbol":"IFFO1","gene_name":"intermediate filament family orphan 1 [Source:HGNC Symbol;Acc:HGNC:24970]","synonyms":"IFFO,HOM-TES-103","biotype":"protein_coding","ncbi_id":"25900","summary":"This gene is a member of the intermediate filament family. Intermediate filaments are proteins which are primordial components of the cytoskeleton and nuclear envelope. The proteins encoded by the members of this gene family are evolutionarily and structurally related but have limited sequence homology, with the exception of the central rod domain. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":6538375,"end":6556083,"strand":-1,"description":"intermediate filament family orphan 1 [Source:HGNC Symbol;Acc:HGNC:24970]"}, {"versioned_ensembl_gene_id":"ENSG00000245667.2","gene_symbol":"AC006064.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6543504,"end":6544931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140497.16","gene_symbol":"SCAMP2","gene_name":"secretory carrier membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:10564]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10066","summary":"This gene product belongs to the SCAMP family of proteins which are secretory carrier membrane proteins. They function as carriers to the cell surface in post-golgi recycling pathways. Different family members are highly related products of distinct genes, and are usually expressed together. These findings suggest that the SCAMPs may function at the same site during vesicular transport rather than in separate pathways. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":74843730,"end":74873365,"strand":-1,"description":"secretory carrier membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:10564]"}, {"versioned_ensembl_gene_id":"ENSG00000248139.2","gene_symbol":"CUL4AP1","gene_name":"cullin 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44027]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129008","summary":null,"start":116425983,"end":116430892,"strand":-1,"description":"cullin 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44027]"}, {"versioned_ensembl_gene_id":"ENSG00000284669.1","gene_symbol":"AC092053.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39148281,"end":39172952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221971.3","gene_symbol":"TTC4P1","gene_name":"tetratricopeptide repeat domain 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12395]","synonyms":"TTC4P","biotype":"processed_pseudogene","ncbi_id":"222052","summary":null,"start":45999621,"end":46000778,"strand":-1,"description":"tetratricopeptide repeat domain 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12395]"}, {"versioned_ensembl_gene_id":"ENSG00000275282.1","gene_symbol":"CFL1P5","gene_name":"cofilin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1877]","synonyms":"CFLP5,CFLL1","biotype":"processed_pseudogene","ncbi_id":"1074","summary":null,"start":69313353,"end":69313854,"strand":-1,"description":"cofilin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1877]"}, {"versioned_ensembl_gene_id":"ENSG00000253771.5","gene_symbol":"TPTE2P1","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35196]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646405","summary":null,"start":24924677,"end":24968487,"strand":-1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35196]"}, {"versioned_ensembl_gene_id":"ENSG00000284048.2","gene_symbol":"AC073111.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":150379329,"end":150410597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232762.1","gene_symbol":"AL355483.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53304536,"end":53307462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234939.1","gene_symbol":"MTND2P18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42119]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873224","summary":null,"start":131384461,"end":131385490,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42119]"}, {"versioned_ensembl_gene_id":"ENSG00000136193.16","gene_symbol":"SCRN1","gene_name":"secernin 1 [Source:HGNC Symbol;Acc:HGNC:22192]","synonyms":"KIAA0193","biotype":"protein_coding","ncbi_id":"9805","summary":"This gene likely encodes a member of the secernin family of proteins. A similar protein in rat functions in regulation of exocytosis in mast cells. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":29920103,"end":29990289,"strand":-1,"description":"secernin 1 [Source:HGNC Symbol;Acc:HGNC:22192]"}, {"versioned_ensembl_gene_id":"ENSG00000233662.1","gene_symbol":"CALM2P4","gene_name":"calmodulin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39661]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643193","summary":null,"start":98640814,"end":98641239,"strand":-1,"description":"calmodulin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39661]"}, {"versioned_ensembl_gene_id":"ENSG00000234796.1","gene_symbol":"AC113607.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":910926,"end":921124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226433.1","gene_symbol":"AP000290.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33156632,"end":33159110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271853.5","gene_symbol":"AL162258.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":153626332,"end":153634340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204359.9","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31985034,"end":31990148,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000115325.13","gene_symbol":"DOK1","gene_name":"docking protein 1 [Source:HGNC Symbol;Acc:HGNC:2990]","synonyms":"p62dok","biotype":"protein_coding","ncbi_id":"1796","summary":"The protein encoded by this gene is part of a signal transduction pathway downstream of receptor tyrosine kinases. The encoded protein is a scaffold protein that helps form a platform for the assembly of multiprotein signaling complexes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":74549026,"end":74557554,"strand":1,"description":"docking protein 1 [Source:HGNC Symbol;Acc:HGNC:2990]"}, {"versioned_ensembl_gene_id":"ENSG00000223747.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31973822,"end":31981098,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000206324.11","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32125820,"end":32135704,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000206331.11","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"C6orf31,NG5,IFITMD7","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32105963,"end":32111974,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000177669.3","gene_symbol":"MBOAT4","gene_name":"membrane bound O-acyltransferase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32311]","synonyms":"OACT4,GOAT,FKSG89","biotype":"protein_coding","ncbi_id":"619373","summary":null,"start":30131824,"end":30144686,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32311]"}, {"versioned_ensembl_gene_id":"ENSG00000133136.4","gene_symbol":"GNG5P2","gene_name":"G protein subunit gamma 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347687","summary":null,"start":110346703,"end":110346909,"strand":-1,"description":"G protein subunit gamma 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24826]"}, {"versioned_ensembl_gene_id":"ENSG00000083168.9","gene_symbol":"KAT6A","gene_name":"lysine acetyltransferase 6A [Source:HGNC Symbol;Acc:HGNC:13013]","synonyms":"ZNF220,ZC2HC6A,RUNXBP2,MYST3,MOZ","biotype":"protein_coding","ncbi_id":"7994","summary":"This gene encodes a member of the MOZ, YBFR2, SAS2, TIP60 family of histone acetyltransferases. The protein is composed of a nuclear localization domain, a double C2H2 zinc finger domain that binds to acetylated histone tails, a histone acetyl-transferase domain, a glutamate/aspartate-rich region, and a serine- and methionine-rich transactivation domain. It is part of a complex that acetylates lysine-9 residues in histone 3, and in addition, it acts as a co-activator for several transcription factors. Allelic variants of this gene are associated with an autosomal dominant form of cognitive disability. Chromosomal translocations of this gene are associated with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":41929479,"end":42051990,"strand":-1,"description":"lysine acetyltransferase 6A [Source:HGNC Symbol;Acc:HGNC:13013]"}, {"versioned_ensembl_gene_id":"ENSG00000137996.12","gene_symbol":"RTCA","gene_name":"RNA 3'-terminal phosphate cyclase [Source:HGNC Symbol;Acc:HGNC:17981]","synonyms":"RTCD1,RTC1,RPC","biotype":"protein_coding","ncbi_id":"8634","summary":"This gene encodes a member of the RNA 3'-phosphate cyclase family. The encoded protein plays a role in RNA metabolism by catalyzing the ATP-dependent conversion of the 3'-phosphate of RNA substrates to a 2',3'-cyclic phosphodiester. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":100266207,"end":100292769,"strand":1,"description":"RNA 3'-terminal phosphate cyclase [Source:HGNC Symbol;Acc:HGNC:17981]"}, {"versioned_ensembl_gene_id":"ENSG00000236958.1","gene_symbol":"AC051618.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":54864674,"end":54869122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249860.3","gene_symbol":"MTRNR2L5","gene_name":"MT-RNR2-like 5 [Source:HGNC Symbol;Acc:HGNC:37162]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463289","summary":null,"start":55599303,"end":55600041,"strand":1,"description":"MT-RNR2-like 5 [Source:HGNC Symbol;Acc:HGNC:37162]"}, {"versioned_ensembl_gene_id":"ENSG00000279727.1","gene_symbol":"LINC02033","gene_name":"long intergenic non-protein coding RNA 2033 [Source:HGNC Symbol;Acc:HGNC:52867]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377031","summary":null,"start":36819276,"end":36822498,"strand":-1,"description":"long intergenic non-protein coding RNA 2033 [Source:HGNC Symbol;Acc:HGNC:52867]"}, {"versioned_ensembl_gene_id":"ENSG00000248488.2","gene_symbol":"PGAM4P2","gene_name":"phosphoglycerate mutase family member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42466]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131611","summary":null,"start":115764099,"end":115764819,"strand":-1,"description":"phosphoglycerate mutase family member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42466]"}, {"versioned_ensembl_gene_id":"ENSG00000172667.10","gene_symbol":"ZMAT3","gene_name":"zinc finger matrin-type 3 [Source:HGNC Symbol;Acc:HGNC:29983]","synonyms":"WIG1,WIG-1,PAG608,MGC10613,FLJ12296","biotype":"protein_coding","ncbi_id":"64393","summary":"This gene encodes a protein containing three zinc finger domains and a nuclear localization signal. The mRNA and the protein of this gene are upregulated by wildtype p53 and overexpression of this gene inhibits tumor cell growth, suggesting that this gene may have a role in the p53-dependent growth regulatory pathway. Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid. [provided by RefSeq, Jul 2008]","start":179017223,"end":179072279,"strand":-1,"description":"zinc finger matrin-type 3 [Source:HGNC Symbol;Acc:HGNC:29983]"}, {"versioned_ensembl_gene_id":"ENSG00000251308.1","gene_symbol":"MRPS33P3","gene_name":"mitochondrial ribosomal protein S33 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29766]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359776","summary":null,"start":115142982,"end":115143303,"strand":1,"description":"mitochondrial ribosomal protein S33 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29766]"}, {"versioned_ensembl_gene_id":"ENSG00000230067.3","gene_symbol":"HSPD1P6","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5267]","synonyms":"HSPDP6,HSPD1-6P","biotype":"transcribed_processed_pseudogene","ncbi_id":"645548","summary":null,"start":36767117,"end":36784167,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:5267]"}, {"versioned_ensembl_gene_id":"ENSG00000241111.1","gene_symbol":"PRICKLE2-AS1","gene_name":"PRICKLE2 antisense RNA 1 [Source:NCBI gene;Acc:100652759]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652759","summary":null,"start":64067964,"end":64103131,"strand":1,"description":"PRICKLE2 antisense RNA 1 [Source:NCBI gene;Acc:100652759]"}, {"versioned_ensembl_gene_id":"ENSG00000248831.2","gene_symbol":"AC008638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77350370,"end":77351235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230010.1","gene_symbol":"AL049646.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18322552,"end":18359300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255700.2","gene_symbol":"APOOP3","gene_name":"apolipoprotein O pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48741]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131528","summary":null,"start":65134688,"end":65135273,"strand":1,"description":"apolipoprotein O pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48741]"}, {"versioned_ensembl_gene_id":"ENSG00000214732.2","gene_symbol":"AL096814.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42155426,"end":42163439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164692.17","gene_symbol":"COL1A2","gene_name":"collagen type I alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2198]","synonyms":"OI4","biotype":"protein_coding","ncbi_id":"1278","summary":"This gene encodes the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]","start":94394561,"end":94431232,"strand":1,"description":"collagen type I alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2198]"}, {"versioned_ensembl_gene_id":"ENSG00000227176.1","gene_symbol":"AC092641.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170077224,"end":170078294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273616.4","gene_symbol":"NDUFA6-AS1","gene_name":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100132273","summary":null,"start":42090956,"end":42125351,"strand":1,"description":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]"}, {"versioned_ensembl_gene_id":"ENSG00000112394.16","gene_symbol":"SLC16A10","gene_name":"solute carrier family 16 member 10 [Source:HGNC Symbol;Acc:HGNC:17027]","synonyms":"TAT1,MCT10","biotype":"protein_coding","ncbi_id":"117247","summary":"SLC16A10 is a member of a family of plasma membrane amino acid transporters that mediate the Na(+)-independent transport of aromatic amino acids across the plasma membrane.[supplied by OMIM, Apr 2004]","start":111087503,"end":111231194,"strand":1,"description":"solute carrier family 16 member 10 [Source:HGNC Symbol;Acc:HGNC:17027]"}, {"versioned_ensembl_gene_id":"ENSG00000231046.1","gene_symbol":"AL360227.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111227747,"end":111259034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166987.14","gene_symbol":"MBD6","gene_name":"methyl-CpG binding domain protein 6 [Source:HGNC Symbol;Acc:HGNC:20445]","synonyms":"KIAA1887","biotype":"protein_coding","ncbi_id":"114785","summary":null,"start":57520710,"end":57530148,"strand":1,"description":"methyl-CpG binding domain protein 6 [Source:HGNC Symbol;Acc:HGNC:20445]"}, {"versioned_ensembl_gene_id":"ENSG00000261394.1","gene_symbol":"AC007598.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12366982,"end":12372582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260488.1","gene_symbol":"AC007216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11976851,"end":11977850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239926.1","gene_symbol":"PRDX3P4","gene_name":"peroxiredoxin 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44643]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418955","summary":null,"start":64174401,"end":64175147,"strand":1,"description":"peroxiredoxin 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44643]"}, {"versioned_ensembl_gene_id":"ENSG00000137312.14","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30727709,"end":30742733,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000143222.11","gene_symbol":"UFC1","gene_name":"ubiquitin-fold modifier conjugating enzyme 1 [Source:HGNC Symbol;Acc:HGNC:26941]","synonyms":"HSPC155","biotype":"protein_coding","ncbi_id":"51506","summary":"UFC1 is an E2-like conjugating enzyme for ubiquitin-fold modifier-1 (UFM1; MIM 610553) (Komatsu et al., 2004 [PubMed 15071506]).[supplied by OMIM, Mar 2008]","start":161152776,"end":161158856,"strand":1,"description":"ubiquitin-fold modifier conjugating enzyme 1 [Source:HGNC Symbol;Acc:HGNC:26941]"}, {"versioned_ensembl_gene_id":"ENSG00000152430.17","gene_symbol":"BOLL","gene_name":"boule homolog, RNA binding protein [Source:HGNC Symbol;Acc:HGNC:14273]","synonyms":"BOULE","biotype":"protein_coding","ncbi_id":"66037","summary":"This gene belongs to the DAZ gene family required for germ cell development. It encodes an RNA-binding protein which is more similar to Drosophila Boule than to human proteins encoded by genes DAZ (deleted in azoospermia) or DAZL (deleted in azoospermia-like). Loss of this gene function results in the absence of sperm in semen (azoospermia). Histological studies demonstrated that the primary defect is at the meiotic G2/M transition. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":197726879,"end":197786762,"strand":-1,"description":"boule homolog, RNA binding protein [Source:HGNC Symbol;Acc:HGNC:14273]"}, {"versioned_ensembl_gene_id":"ENSG00000116120.9","gene_symbol":"FARSB","gene_name":"phenylalanyl-tRNA synthetase beta subunit [Source:HGNC Symbol;Acc:HGNC:17800]","synonyms":"PheHB,FRSB,FARSLB","biotype":"protein_coding","ncbi_id":"10056","summary":"This gene encodes a highly conserved enzyme that belongs to the aminoacyl-tRNA synthetase class IIc subfamily. This enzyme comprises the regulatory beta subunits that form a tetramer with two catalytic alpha subunits. In the presence of ATP, this tetramer is responsible for attaching L-phenylalanine to the terminal adenosine of the appropriate tRNA. A pseudogene located on chromosome 10 has been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":222570536,"end":222656337,"strand":-1,"description":"phenylalanyl-tRNA synthetase beta subunit [Source:HGNC Symbol;Acc:HGNC:17800]"}, {"versioned_ensembl_gene_id":"ENSG00000274518.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"cl-49,nkat5,183ActI,CD158J","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738519,"end":54752638,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000249071.2","gene_symbol":"EGFLAM-AS3","gene_name":"EGFLAM antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:41167]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874116","summary":null,"start":38345347,"end":38346551,"strand":-1,"description":"EGFLAM antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:41167]"}, {"versioned_ensembl_gene_id":"ENSG00000249491.1","gene_symbol":"EGFLAM-AS1","gene_name":"EGFLAM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41169]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874117","summary":null,"start":38425036,"end":38427376,"strand":-1,"description":"EGFLAM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41169]"}, {"versioned_ensembl_gene_id":"ENSG00000107863.17","gene_symbol":"ARHGAP21","gene_name":"Rho GTPase activating protein 21 [Source:HGNC Symbol;Acc:HGNC:23725]","synonyms":"KIAA1424,ARHGAP10","biotype":"protein_coding","ncbi_id":"57584","summary":"ARHGAP21 functions preferentially as a GTPase-activating protein (GAP) for CDC42 (MIM 116952) and regulates the ARP2/3 complex (MIM 604221) and F-actin dynamics at the Golgi through control of CDC42 activity (Dubois et al., 2005 [PubMed 15793564]).[supplied by OMIM, Mar 2008]","start":24583609,"end":24723668,"strand":-1,"description":"Rho GTPase activating protein 21 [Source:HGNC Symbol;Acc:HGNC:23725]"}, {"versioned_ensembl_gene_id":"ENSG00000244545.1","gene_symbol":"AC092924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152648146,"end":152650447,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241451.2","gene_symbol":"RPS27P22","gene_name":"ribosomal protein S27 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36090]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131418","summary":null,"start":22722229,"end":22722469,"strand":1,"description":"ribosomal protein S27 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36090]"}, {"versioned_ensembl_gene_id":"ENSG00000163082.9","gene_symbol":"SGPP2","gene_name":"sphingosine-1-phosphate phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:19953]","synonyms":"SPP2,FLJ39004","biotype":"protein_coding","ncbi_id":"130367","summary":"The protein encoded by this gene is a transmembrane protein that degrades the bioactive signaling molecule sphingosine 1-phosphate. The encoded protein is induced during inflammatory responses and has been shown to be downregulated by the microRNA-31 tumor suppressor. Alternative splice variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2016]","start":222424517,"end":222560948,"strand":1,"description":"sphingosine-1-phosphate phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:19953]"}, {"versioned_ensembl_gene_id":"ENSG00000136695.14","gene_symbol":"IL36RN","gene_name":"interleukin 36 receptor antagonist [Source:HGNC Symbol;Acc:HGNC:15561]","synonyms":"IL1HY1,IL1F5,IL-1F5,FIL1D,FIL1(DELTA),MGC29840,FIL1,IL36RA,IL1RP3,IL1L1","biotype":"protein_coding","ncbi_id":"26525","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine was shown to specifically inhibit the activation of NF-kappaB induced by interleukin 1 family, member 6 (IL1F6). This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. Two alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":113058638,"end":113065382,"strand":1,"description":"interleukin 36 receptor antagonist [Source:HGNC Symbol;Acc:HGNC:15561]"}, {"versioned_ensembl_gene_id":"ENSG00000256737.1","gene_symbol":"RBBP4P5","gene_name":"RB binding protein 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42372]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288451","summary":null,"start":21563819,"end":21565084,"strand":1,"description":"RB binding protein 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42372]"}, {"versioned_ensembl_gene_id":"ENSG00000271200.1","gene_symbol":"AC099791.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61741998,"end":61742424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230327.1","gene_symbol":"MTCO1P42","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075283","summary":null,"start":50588690,"end":50589415,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52107]"}, {"versioned_ensembl_gene_id":"ENSG00000177485.6","gene_symbol":"ZBTB33","gene_name":"zinc finger and BTB domain containing 33 [Source:HGNC Symbol;Acc:HGNC:16682]","synonyms":"ZNF348,ZNF-kaiso,WUGSC:H_DJ525N14.1,kaiso","biotype":"protein_coding","ncbi_id":"10009","summary":"This gene encodes a transcriptional regulator with bimodal DNA-binding specificity, which binds to methylated CGCG and also to the non-methylated consensus KAISO-binding site TCCTGCNA. The protein contains an N-terminal POZ/BTB domain and 3 C-terminal zinc finger motifs. It recruits the N-CoR repressor complex to promote histone deacetylation and the formation of repressive chromatin structures in target gene promoters. It may contribute to the repression of target genes of the Wnt signaling pathway, and may also activate transcription of a subset of target genes by the recruitment of catenin delta-2 (CTNND2). Its interaction with catenin delta-1 (CTNND1) inhibits binding to both methylated and non-methylated DNA. It also interacts directly with the nuclear import receptor Importin-α2 (also known as karyopherin alpha2 or RAG cohort 1), which may mediate nuclear import of this protein. Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq, May 2010]","start":120250752,"end":120258398,"strand":1,"description":"zinc finger and BTB domain containing 33 [Source:HGNC Symbol;Acc:HGNC:16682]"}, {"versioned_ensembl_gene_id":"ENSG00000271415.1","gene_symbol":"RPL23AP90","gene_name":"ribosomal protein L23a pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:51624]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480690","summary":null,"start":100196816,"end":100197051,"strand":1,"description":"ribosomal protein L23a pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:51624]"}, {"versioned_ensembl_gene_id":"ENSG00000124155.17","gene_symbol":"PIGT","gene_name":"phosphatidylinositol glycan anchor biosynthesis class T [Source:HGNC Symbol;Acc:HGNC:14938]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51604","summary":"This gene encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This protein is an essential component of the multisubunit enzyme, GPI transamidase. GPI transamidase mediates GPI anchoring in the endoplasmic reticulum, by catalyzing the transfer of fully assembled GPI units to proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":45416067,"end":45456934,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class T [Source:HGNC Symbol;Acc:HGNC:14938]"}, {"versioned_ensembl_gene_id":"ENSG00000151849.14","gene_symbol":"CENPJ","gene_name":"centromere protein J [Source:HGNC Symbol;Acc:HGNC:17272]","synonyms":"LAP,CPAP,BM032,SCKL4,SASS4,Sas-4,MCPH6,LIP1","biotype":"protein_coding","ncbi_id":"55835","summary":"This gene encodes a protein that belongs to the centromere protein family. During cell division, this protein plays a structural role in the maintenance of centrosome integrity and normal spindle morphology, and it is involved in microtubule disassembly at the centrosome. This protein can function as a transcriptional coactivator in the Stat5 signaling pathway, and also as a coactivator of NF-kappaB-mediated transcription, likely via its interaction with the coactivator p300/CREB-binding protein. Mutations in this gene are associated with primary autosomal recessive microcephaly, a disorder characterized by severely reduced brain size and cognitive disability. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2012]","start":24882284,"end":24922889,"strand":-1,"description":"centromere protein J [Source:HGNC Symbol;Acc:HGNC:17272]"}, {"versioned_ensembl_gene_id":"ENSG00000111860.13","gene_symbol":"CEP85L","gene_name":"centrosomal protein 85 like [Source:HGNC Symbol;Acc:HGNC:21638]","synonyms":"NY-BR-15,C6orf204,bA57K17.2","biotype":"protein_coding","ncbi_id":"387119","summary":"The protein encoded by this gene was identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":118460772,"end":118710075,"strand":-1,"description":"centrosomal protein 85 like [Source:HGNC Symbol;Acc:HGNC:21638]"}, {"versioned_ensembl_gene_id":"ENSG00000151576.10","gene_symbol":"QTRT2","gene_name":"queuine tRNA-ribosyltransferase accessory subunit 2 [Source:HGNC Symbol;Acc:HGNC:25771]","synonyms":"QTRTD1,FLJ12960","biotype":"protein_coding","ncbi_id":"79691","summary":"This gene encodes a subunit of tRNA-guanine transglycosylase. tRNA-guanine transglycosylase is a heterodimeric enzyme complex that plays a critical role in tRNA modification by synthesizing the 7-deazaguanosine queuosine, which is found in tRNAs that code for asparagine, aspartic acid, histidine, and tyrosine. The encoded protein may play a role in the queuosine 5'-monophosphate salvage pathway. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":114005833,"end":114088422,"strand":1,"description":"queuine tRNA-ribosyltransferase accessory subunit 2 [Source:HGNC Symbol;Acc:HGNC:25771]"}, {"versioned_ensembl_gene_id":"ENSG00000267034.1","gene_symbol":"AC010980.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":222317242,"end":222318653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225913.2","gene_symbol":"AL138767.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87607985,"end":87659279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198857.3","gene_symbol":"HSD3BP5","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5223]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"391081","summary":null,"start":119601340,"end":119609250,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5223]"}, {"versioned_ensembl_gene_id":"ENSG00000115649.15","gene_symbol":"CNPPD1","gene_name":"cyclin Pas1/PHO80 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25220]","synonyms":"CGI-57,C2orf24","biotype":"protein_coding","ncbi_id":"27013","summary":null,"start":219171897,"end":219178106,"strand":-1,"description":"cyclin Pas1/PHO80 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25220]"}, {"versioned_ensembl_gene_id":"ENSG00000145908.12","gene_symbol":"ZNF300","gene_name":"zinc finger protein 300 [Source:HGNC Symbol;Acc:HGNC:13091]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91975","summary":"The protein encoded by this gene is a C2H2-type zinc finger DNA binding protein and likely transcriptional regulator. The function of this protein is not yet known. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]","start":150894392,"end":150904983,"strand":-1,"description":"zinc finger protein 300 [Source:HGNC Symbol;Acc:HGNC:13091]"}, {"versioned_ensembl_gene_id":"ENSG00000282768.1","gene_symbol":"AC131056.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36336091,"end":36336195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126001.15","gene_symbol":"CEP250","gene_name":"centrosomal protein 250 [Source:HGNC Symbol;Acc:HGNC:1859]","synonyms":"CEP2,C-NAP1","biotype":"protein_coding","ncbi_id":"11190","summary":"This gene encodes a core centrosomal protein required for centriole-centriole cohesion during interphase of the cell cycle. The encoded protein dissociates from the centrosomes when parental centrioles separate at the beginning of mitosis. The protein associates with and is phosphorylated by NIMA-related kinase 2, which is also associated with the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":35455164,"end":35519280,"strand":1,"description":"centrosomal protein 250 [Source:HGNC Symbol;Acc:HGNC:1859]"}, {"versioned_ensembl_gene_id":"ENSG00000243069.7","gene_symbol":"ARHGEF26-AS1","gene_name":"ARHGEF26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41048]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507524","summary":null,"start":154024401,"end":154121332,"strand":-1,"description":"ARHGEF26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41048]"}, {"versioned_ensembl_gene_id":"ENSG00000173209.22","gene_symbol":"AHSA2","gene_name":"activator of HSP90 ATPase homolog 2 [Source:HGNC Symbol;Acc:HGNC:20437]","synonyms":"Hch1,DKFZp564C236,AHA1","biotype":"protein_coding","ncbi_id":"130872","summary":null,"start":61177418,"end":61191203,"strand":1,"description":"activator of HSP90 ATPase homolog 2 [Source:HGNC Symbol;Acc:HGNC:20437]"}, {"versioned_ensembl_gene_id":"ENSG00000274945.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54848094,"end":54859121,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000247556.6","gene_symbol":"OIP5-AS1","gene_name":"OIP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43563]","synonyms":"linc-OIP5,cyrano","biotype":"processed_transcript","ncbi_id":"729082","summary":"This is a conserved gene that produces a long non-coding RNA that maintains cell proliferation in embryonic stem cells. This RNA can bind to and negatively regulate the activity of multiple cellular RNAs and microRNAs, including cyclin G associated kinase and ELAV like RNA binding protein 1. [provided by RefSeq, Dec 2017]","start":41283990,"end":41309737,"strand":1,"description":"OIP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43563]"}, {"versioned_ensembl_gene_id":"ENSG00000275401.1","gene_symbol":"AL391095.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38418483,"end":38419202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278058.1","gene_symbol":"AC009159.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79605802,"end":79606605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267469.1","gene_symbol":"AC005944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3052910,"end":3053724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260941.1","gene_symbol":"LINC00622","gene_name":"long intergenic non-protein coding RNA 622 [Source:HGNC Symbol;Acc:HGNC:44251]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"644242","summary":null,"start":119597702,"end":119599271,"strand":-1,"description":"long intergenic non-protein coding RNA 622 [Source:HGNC Symbol;Acc:HGNC:44251]"}, {"versioned_ensembl_gene_id":"ENSG00000101624.10","gene_symbol":"CEP76","gene_name":"centrosomal protein 76 [Source:HGNC Symbol;Acc:HGNC:25727]","synonyms":"HsT1705,FLJ12542,C18orf9","biotype":"protein_coding","ncbi_id":"79959","summary":"This gene encodes a centrosomal protein which regulates centriole amplification by limiting centriole duplication to once per cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":12661833,"end":12702777,"strand":-1,"description":"centrosomal protein 76 [Source:HGNC Symbol;Acc:HGNC:25727]"}, {"versioned_ensembl_gene_id":"ENSG00000234813.1","gene_symbol":"AL357520.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18940501,"end":18940953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262003.1","gene_symbol":"AC087392.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":909632,"end":911212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133131.14","gene_symbol":"MORC4","gene_name":"MORC family CW-type zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:23485]","synonyms":"FLJ11565,ZCWCC2,ZCW4","biotype":"protein_coding","ncbi_id":"79710","summary":"In human, the four current members of the microrchidia (morc) gene family share an N-terminal ATPase-like ATP-binding region and a CW four-cysteine zinc-finger motif. The protein encoded by this gene also has a nuclear matrix binding domain and a two-stranded coiled-coil motif near its C-terminus. This gene is widely expressed at low levels in normal tissues and has elevated expression in placenta and testis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010]","start":106813871,"end":107000244,"strand":-1,"description":"MORC family CW-type zinc finger 4 [Source:HGNC Symbol;Acc:HGNC:23485]"}, {"versioned_ensembl_gene_id":"ENSG00000284738.1","gene_symbol":"AL358472.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153923337,"end":153935240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164978.17","gene_symbol":"NUDT2","gene_name":"nudix hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:8049]","synonyms":"APAH1","biotype":"protein_coding","ncbi_id":"318","summary":"This gene encodes a member of the MutT family of nucleotide pyrophosphatases, a subset of the larger NUDIX hydrolase family. The gene product possesses a modification of the MutT sequence motif found in certain nucleotide pyrophosphatases. The enzyme asymmetrically hydrolyzes Ap4A to yield AMP and ATP and is responsible for maintaining the intracellular level of the dinucleotide Ap4A, the function of which has yet to be established. This gene may be a candidate tumor suppressor gene. Alternative splicing has been observed at this locus and four transcript variants, all encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]","start":34329506,"end":34343713,"strand":1,"description":"nudix hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:8049]"}, {"versioned_ensembl_gene_id":"ENSG00000278983.1","gene_symbol":"AC048380.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48564795,"end":48568342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280882.1","gene_symbol":"AP000432.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17705408,"end":17707455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167992.12","gene_symbol":"VWCE","gene_name":"von Willebrand factor C and EGF domains [Source:HGNC Symbol;Acc:HGNC:26487]","synonyms":"VWC1,URG11,FLJ32009","biotype":"protein_coding","ncbi_id":"220001","summary":null,"start":61258286,"end":61295424,"strand":-1,"description":"von Willebrand factor C and EGF domains [Source:HGNC Symbol;Acc:HGNC:26487]"}, {"versioned_ensembl_gene_id":"ENSG00000113088.5","gene_symbol":"GZMK","gene_name":"granzyme K [Source:HGNC Symbol;Acc:HGNC:4711]","synonyms":"TRYP2,PRSS","biotype":"protein_coding","ncbi_id":"3003","summary":"This gene product is a member of a group of related serine proteases from the cytoplasmic granules of cytotoxic lymphocytes. Cytolytic T lymphocytes (CTL) and natural killer (NK) cells share the remarkable ability to recognize, bind, and lyse specific target cells. They are thought to protect their host by lysing cells bearing on their surface 'nonself' antigens, usually peptides or proteins resulting from infection by intracellular pathogens. The protein described here lacks consensus sequences for N-glycosylation present in other granzymes. [provided by RefSeq, Jul 2008]","start":55024253,"end":55034570,"strand":1,"description":"granzyme K [Source:HGNC Symbol;Acc:HGNC:4711]"}, {"versioned_ensembl_gene_id":"ENSG00000248716.2","gene_symbol":"AC093815.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114103938,"end":114104225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259291.2","gene_symbol":"ZNF710-AS1","gene_name":"ZNF710 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53141]","synonyms":"ENST00000558334","biotype":"antisense_RNA","ncbi_id":"109729181","summary":null,"start":90074512,"end":90082207,"strand":-1,"description":"ZNF710 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53141]"}, {"versioned_ensembl_gene_id":"ENSG00000203463.2","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"processed_transcript","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31902815,"end":31903058,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000169271.2","gene_symbol":"HSPB3","gene_name":"heat shock protein family B (small) member 3 [Source:HGNC Symbol;Acc:HGNC:5248]","synonyms":"HSPL27","biotype":"protein_coding","ncbi_id":"8988","summary":"This gene encodes a muscle-specific small heat shock protein. A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C.[provided by RefSeq, Sep 2010]","start":54455601,"end":54456384,"strand":1,"description":"heat shock protein family B (small) member 3 [Source:HGNC Symbol;Acc:HGNC:5248]"}, {"versioned_ensembl_gene_id":"ENSG00000186684.12","gene_symbol":"CYP27C1","gene_name":"cytochrome P450 family 27 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:33480]","synonyms":"FLJ16008","biotype":"protein_coding","ncbi_id":"339761","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. [provided by RefSeq, Jul 2008]","start":127184120,"end":127220078,"strand":-1,"description":"cytochrome P450 family 27 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:33480]"}, {"versioned_ensembl_gene_id":"ENSG00000181192.11","gene_symbol":"DHTKD1","gene_name":"dehydrogenase E1 and transketolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23537]","synonyms":"MGC3090,KIAA1630,DKFZP762M115,CMT2Q","biotype":"protein_coding","ncbi_id":"55526","summary":"This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria and Charcot-Marie-Tooth Disease Type 2Q. [provided by RefSeq, May 2013]","start":12068972,"end":12123225,"strand":1,"description":"dehydrogenase E1 and transketolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23537]"}, {"versioned_ensembl_gene_id":"ENSG00000238755.3","gene_symbol":"LINC02006","gene_name":"long intergenic non-protein coding RNA 2006 [Source:HGNC Symbol;Acc:HGNC:52842]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"105374165","summary":null,"start":153384934,"end":153980186,"strand":-1,"description":"long intergenic non-protein coding RNA 2006 [Source:HGNC Symbol;Acc:HGNC:52842]"}, {"versioned_ensembl_gene_id":"ENSG00000243486.1","gene_symbol":"AC068985.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153881526,"end":153940836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243012.1","gene_symbol":"LINC02083","gene_name":"long intergenic non-protein coding RNA 2083 [Source:HGNC Symbol;Acc:HGNC:52933]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986147","summary":null,"start":153431856,"end":153443531,"strand":1,"description":"long intergenic non-protein coding RNA 2083 [Source:HGNC Symbol;Acc:HGNC:52933]"}, {"versioned_ensembl_gene_id":"ENSG00000237787.4","gene_symbol":"C3orf79","gene_name":"chromosome 3 open reading frame 79 [Source:HGNC Symbol;Acc:HGNC:37259]","synonyms":null,"biotype":"lincRNA","ncbi_id":"152118","summary":null,"start":153484495,"end":153502697,"strand":1,"description":"chromosome 3 open reading frame 79 [Source:HGNC Symbol;Acc:HGNC:37259]"}, {"versioned_ensembl_gene_id":"ENSG00000224344.1","gene_symbol":"KNOP1P3","gene_name":"lysine rich nucleolar protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128029","summary":null,"start":51511058,"end":51511483,"strand":1,"description":"lysine rich nucleolar protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48921]"}, {"versioned_ensembl_gene_id":"ENSG00000259759.1","gene_symbol":"AC007907.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54239693,"end":54240654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231918.1","gene_symbol":"AC007402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51032601,"end":52407917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256311.1","gene_symbol":"AC084880.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119225834,"end":119259017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261501.1","gene_symbol":"AC079341.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121870583,"end":121872848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225444.1","gene_symbol":"LINC01867","gene_name":"long intergenic non-protein coding RNA 1867 [Source:HGNC Symbol;Acc:HGNC:52687]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374596","summary":null,"start":52373118,"end":52390012,"strand":1,"description":"long intergenic non-protein coding RNA 1867 [Source:HGNC Symbol;Acc:HGNC:52687]"}, {"versioned_ensembl_gene_id":"ENSG00000259517.2","gene_symbol":"LINC02169","gene_name":"long intergenic non-protein coding RNA 2169 [Source:HGNC Symbol;Acc:HGNC:53031]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996338","summary":null,"start":54245618,"end":54270746,"strand":-1,"description":"long intergenic non-protein coding RNA 2169 [Source:HGNC Symbol;Acc:HGNC:53031]"}, {"versioned_ensembl_gene_id":"ENSG00000238165.1","gene_symbol":"AC007560.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50829442,"end":50829678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146858.7","gene_symbol":"ZC3HAV1L","gene_name":"zinc finger CCCH-type containing, antiviral 1 like [Source:HGNC Symbol;Acc:HGNC:22423]","synonyms":"MGC14289,C7orf39","biotype":"protein_coding","ncbi_id":"92092","summary":null,"start":139025706,"end":139036029,"strand":-1,"description":"zinc finger CCCH-type containing, antiviral 1 like [Source:HGNC Symbol;Acc:HGNC:22423]"}, {"versioned_ensembl_gene_id":"ENSG00000281196.1","gene_symbol":"LINC00934","gene_name":"long intergenic non-protein coding RNA 934 [Source:NCBI gene;Acc:144742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"144742","summary":null,"start":119283825,"end":119303380,"strand":-1,"description":"long intergenic non-protein coding RNA 934 [Source:NCBI gene;Acc:144742]"}, {"versioned_ensembl_gene_id":"ENSG00000226366.1","gene_symbol":"AC097463.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51926882,"end":51927362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236538.1","gene_symbol":"ZNF863P","gene_name":"zinc finger protein 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:35156]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419682","summary":null,"start":52071355,"end":52077197,"strand":1,"description":"zinc finger protein 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:35156]"}, {"versioned_ensembl_gene_id":"ENSG00000225140.1","gene_symbol":"AL358216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":628638,"end":631255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233021.2","gene_symbol":"AL669841.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":437561,"end":441170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077009.13","gene_symbol":"NMRK2","gene_name":"nicotinamide riboside kinase 2 [Source:HGNC Symbol;Acc:HGNC:17871]","synonyms":"NRK2,MIBP,ITGB1BP3","biotype":"protein_coding","ncbi_id":"27231","summary":null,"start":3933103,"end":3942416,"strand":1,"description":"nicotinamide riboside kinase 2 [Source:HGNC Symbol;Acc:HGNC:17871]"}, {"versioned_ensembl_gene_id":"ENSG00000230840.1","gene_symbol":"AC097463.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51925692,"end":51925833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177508.11","gene_symbol":"IRX3","gene_name":"iroquois homeobox 3 [Source:HGNC Symbol;Acc:HGNC:14360]","synonyms":"IRX-1","biotype":"protein_coding","ncbi_id":"79191","summary":"IRX3 is a member of the Iroquois homeobox gene family (see IRX1; MIM 606197) and plays a role in an early step of neural development (Bellefroid et al., 1998 [PubMed 9427753]). Members of this family appear to play multiple roles during pattern formation of vertebrate embryos (Lewis et al., 1999 [PubMed 10370142]).[supplied by OMIM, Aug 2009]","start":54283304,"end":54286763,"strand":-1,"description":"iroquois homeobox 3 [Source:HGNC Symbol;Acc:HGNC:14360]"}, {"versioned_ensembl_gene_id":"ENSG00000180525.11","gene_symbol":"PRR26","gene_name":"proline rich 26 [Source:HGNC Symbol;Acc:HGNC:30724]","synonyms":"FLJ38681,C10orf108","biotype":"protein_coding","ncbi_id":"414235","summary":null,"start":649948,"end":669581,"strand":1,"description":"proline rich 26 [Source:HGNC Symbol;Acc:HGNC:30724]"}, {"versioned_ensembl_gene_id":"ENSG00000064687.12","gene_symbol":"ABCA7","gene_name":"ATP binding cassette subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:37]","synonyms":"ABCX","biotype":"protein_coding","ncbi_id":"10347","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This full transporter has been detected predominantly in myelo-lymphatic tissues with the highest expression in peripheral leukocytes, thymus, spleen, and bone marrow. The function of this protein is not yet known; however, the expression pattern suggests a role in lipid homeostasis in cells of the immune system. [provided by RefSeq, Jul 2008]","start":1040101,"end":1065572,"strand":1,"description":"ATP binding cassette subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:37]"}, {"versioned_ensembl_gene_id":"ENSG00000164684.13","gene_symbol":"ZNF704","gene_name":"zinc finger protein 704 [Source:HGNC Symbol;Acc:HGNC:32291]","synonyms":"Gig1,FLJ16218","biotype":"protein_coding","ncbi_id":"619279","summary":null,"start":80628451,"end":80874781,"strand":-1,"description":"zinc finger protein 704 [Source:HGNC Symbol;Acc:HGNC:32291]"}, {"versioned_ensembl_gene_id":"ENSG00000186193.8","gene_symbol":"SAPCD2","gene_name":"suppressor APC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28055]","synonyms":"p42.3,C9orf140","biotype":"protein_coding","ncbi_id":"89958","summary":null,"start":137062124,"end":137070588,"strand":-1,"description":"suppressor APC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28055]"}, {"versioned_ensembl_gene_id":"ENSG00000168394.10","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32845209,"end":32853978,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000118816.9","gene_symbol":"CCNI","gene_name":"cyclin I [Source:HGNC Symbol;Acc:HGNC:1595]","synonyms":"CCNI1","biotype":"protein_coding","ncbi_id":"10983","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin shows the highest similarity with cyclin G. The transcript of this gene was found to be expressed constantly during cell cycle progression. [provided by RefSeq, Jan 2017]","start":77047158,"end":77076005,"strand":-1,"description":"cyclin I [Source:HGNC Symbol;Acc:HGNC:1595]"}, {"versioned_ensembl_gene_id":"ENSG00000179915.22","gene_symbol":"NRXN1","gene_name":"neurexin 1 [Source:HGNC Symbol;Acc:HGNC:8008]","synonyms":"Hs.22998,KIAA0578","biotype":"protein_coding","ncbi_id":"9378","summary":"This gene encodes a single-pass type I membrane protein that belongs to the neurexin family. Neurexins are cell-surface receptors that bind neuroligins to form Ca(2+)-dependent neurexin/neuroligin complexes at synapses in the central nervous system. This complex is required for efficient neurotransmission and is involved in the formation of synaptic contacts. Three members of this gene family have been studied in detail and are estimated to generate over 3,000 variants through the use of two alternative promoters (alpha and beta) and extensive alternative splicing in each family member. Recently, a third promoter (gamma) was identified for this gene in the 3' region. Mutations in this gene are associated with Pitt-Hopkins-like syndrome-2 and may contribute to susceptibility to schizophrenia. [provided by RefSeq, Aug 2016]","start":49918505,"end":51225575,"strand":-1,"description":"neurexin 1 [Source:HGNC Symbol;Acc:HGNC:8008]"}, {"versioned_ensembl_gene_id":"ENSG00000151240.16","gene_symbol":"DIP2C","gene_name":"disco interacting protein 2 homolog C [Source:HGNC Symbol;Acc:HGNC:29150]","synonyms":"KIAA0934","biotype":"protein_coding","ncbi_id":"22982","summary":"This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]","start":274190,"end":689668,"strand":-1,"description":"disco interacting protein 2 homolog C [Source:HGNC Symbol;Acc:HGNC:29150]"}, {"versioned_ensembl_gene_id":"ENSG00000103148.15","gene_symbol":"NPRL3","gene_name":"NPR3 like, GATOR1 complex subunit [Source:HGNC Symbol;Acc:HGNC:14124]","synonyms":"RMD11,NPR3,MARE,HS-40,CGTHBA,C16orf35","biotype":"protein_coding","ncbi_id":"8131","summary":"The function of the encoded protein is not known. [provided by RefSeq, Aug 2011]","start":84271,"end":138860,"strand":-1,"description":"NPR3 like, GATOR1 complex subunit [Source:HGNC Symbol;Acc:HGNC:14124]"}, {"versioned_ensembl_gene_id":"ENSG00000223965.2","gene_symbol":"ZNF587P1","gene_name":"zinc finger protein 587 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42438]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419751","summary":null,"start":31794470,"end":31796175,"strand":1,"description":"zinc finger protein 587 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42438]"}, {"versioned_ensembl_gene_id":"ENSG00000144645.13","gene_symbol":"OSBPL10","gene_name":"oxysterol binding protein like 10 [Source:HGNC Symbol;Acc:HGNC:16395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114884","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Like most members, the encoded protein contains an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":31657890,"end":32077580,"strand":-1,"description":"oxysterol binding protein like 10 [Source:HGNC Symbol;Acc:HGNC:16395]"}, {"versioned_ensembl_gene_id":"ENSG00000283689.1","gene_symbol":"AC018553.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54285604,"end":54289568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123124.13","gene_symbol":"WWP1","gene_name":"WW domain containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:17004]","synonyms":"DKFZP434D2111,AIP5","biotype":"protein_coding","ncbi_id":"11059","summary":"WW domain-containing proteins are found in all eukaryotes and play an important role in the regulation of a wide variety of cellular functions such as protein degradation, transcription, and RNA splicing. This gene encodes a protein which contains 4 tandem WW domains and a HECT (homologous to the E6-associated protein carboxyl terminus) domain. The encoded protein belongs to a family of NEDD4-like proteins, which are E3 ubiquitin-ligase molecules and regulate key trafficking decisions, including targeting of proteins to proteosomes or lysosomes. Alternative splicing of this gene generates at least 6 transcript variants; however, the full length nature of these transcripts has not been defined. [provided by RefSeq, Jul 2008]","start":86342738,"end":86478420,"strand":1,"description":"WW domain containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:17004]"}, {"versioned_ensembl_gene_id":"ENSG00000264424.1","gene_symbol":"MYH4","gene_name":"myosin heavy chain 4 [Source:HGNC Symbol;Acc:HGNC:7574]","synonyms":"MyHC-IIb,MyHC-2B,MYH2B","biotype":"protein_coding","ncbi_id":"4622","summary":null,"start":10443290,"end":10469559,"strand":-1,"description":"myosin heavy chain 4 [Source:HGNC Symbol;Acc:HGNC:7574]"}, {"versioned_ensembl_gene_id":"ENSG00000240752.1","gene_symbol":"AC055731.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78758974,"end":78759374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106012.17","gene_symbol":"IQCE","gene_name":"IQ motif containing E [Source:HGNC Symbol;Acc:HGNC:29171]","synonyms":"KIAA1023","biotype":"protein_coding","ncbi_id":"23288","summary":null,"start":2558972,"end":2614734,"strand":1,"description":"IQ motif containing E [Source:HGNC Symbol;Acc:HGNC:29171]"}, {"versioned_ensembl_gene_id":"ENSG00000223920.2","gene_symbol":"AC099791.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61654194,"end":61654908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227663.1","gene_symbol":"RPL7P2","gene_name":"ribosomal protein L7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16336]","synonyms":"bA550O8.1","biotype":"processed_pseudogene","ncbi_id":"140695","summary":null,"start":2075555,"end":2075822,"strand":1,"description":"ribosomal protein L7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16336]"}, {"versioned_ensembl_gene_id":"ENSG00000260017.1","gene_symbol":"AC138811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18803083,"end":18812181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253516.1","gene_symbol":"HMGB1P41","gene_name":"high mobility group box 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:39188]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873896","summary":null,"start":80812142,"end":80812581,"strand":-1,"description":"high mobility group box 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:39188]"}, {"versioned_ensembl_gene_id":"ENSG00000254331.1","gene_symbol":"CKS1BP7","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:1999]","synonyms":"CKS1,CKS1A","biotype":"processed_pseudogene","ncbi_id":"137529","summary":null,"start":80644939,"end":80645173,"strand":-1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:1999]"}, {"versioned_ensembl_gene_id":"ENSG00000274842.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000236125.3","gene_symbol":"USP17L4","gene_name":"ubiquitin specific peptidase 17-like family member 4 [Source:HGNC Symbol;Acc:HGNC:37176]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645402","summary":null,"start":7337115,"end":7338707,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 4 [Source:HGNC Symbol;Acc:HGNC:37176]"}, {"versioned_ensembl_gene_id":"ENSG00000002745.12","gene_symbol":"WNT16","gene_name":"Wnt family member 16 [Source:HGNC Symbol;Acc:HGNC:16267]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51384","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It contains two transcript variants diverging at the 5' termini. These two variants are proposed to be the products of separate promoters and not to be splice variants from a single promoter. They are differentially expressed in normal tissues, one of which (variant 2) is expressed at significant levels only in the pancreas, whereas another one (variant 1) is expressed more ubiquitously with highest levels in adult kidney, placenta, brain, heart, and spleen. [provided by RefSeq, Jul 2008]","start":121325367,"end":121341104,"strand":1,"description":"Wnt family member 16 [Source:HGNC Symbol;Acc:HGNC:16267]"}, {"versioned_ensembl_gene_id":"ENSG00000143630.9","gene_symbol":"HCN3","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Source:HGNC Symbol;Acc:HGNC:19183]","synonyms":"KIAA1535","biotype":"protein_coding","ncbi_id":"57657","summary":"This gene encodes a multi-pass membrane protein that functions as a voltage gated cation channel. The encoded protein is a member of a family of closely related cyclic adenosine monophosphate-binding channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":155277583,"end":155289848,"strand":1,"description":"hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Source:HGNC Symbol;Acc:HGNC:19183]"}, {"versioned_ensembl_gene_id":"ENSG00000125657.4","gene_symbol":"TNFSF9","gene_name":"TNF superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:11939]","synonyms":"4-1BB-L","biotype":"protein_coding","ncbi_id":"8744","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This transmembrane cytokine is a bidirectional signal transducer that acts as a ligand for TNFRSF9/4-1BB, which is a costimulatory receptor molecule in T lymphocytes. This cytokine and its receptor are involved in the antigen presentation process and in the generation of cytotoxic T cells. The receptor TNFRSF9/4-1BB is absent from resting T lymphocytes but rapidly expressed upon antigenic stimulation. The ligand encoded by this gene, TNFSF9/4-1BBL, has been shown to reactivate anergic T lymphocytes in addition to promoting T lymphocyte proliferation. This cytokine has also been shown to be required for the optimal CD8 responses in CD8 T cells. This cytokine is expressed in carcinoma cell lines, and is thought to be involved in T cell-tumor cell interaction.[provided by RefSeq, Oct 2008]","start":6530999,"end":6535928,"strand":1,"description":"TNF superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:11939]"}, {"versioned_ensembl_gene_id":"ENSG00000273302.1","gene_symbol":"AC016747.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":61199979,"end":61200769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271146.1","gene_symbol":"AC018889.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61249780,"end":61250621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115464.14","gene_symbol":"USP34","gene_name":"ubiquitin specific peptidase 34 [Source:HGNC Symbol;Acc:HGNC:20066]","synonyms":"KIAA0729,KIAA0570","biotype":"protein_coding","ncbi_id":"9736","summary":null,"start":61187463,"end":61470769,"strand":-1,"description":"ubiquitin specific peptidase 34 [Source:HGNC Symbol;Acc:HGNC:20066]"}, {"versioned_ensembl_gene_id":"ENSG00000272434.1","gene_symbol":"AC137630.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49029316,"end":49029706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178035.11","gene_symbol":"IMPDH2","gene_name":"inosine monophosphate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:6053]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3615","summary":"This gene encodes the rate-limiting enzyme in the de novo guanine nucleotide biosynthesis. It is thus involved in maintaining cellular guanine deoxy- and ribonucleotide pools needed for DNA and RNA synthesis. The encoded protein catalyzes the NAD-dependent oxidation of inosine-5'-monophosphate into xanthine-5'-monophosphate, which is then converted into guanosine-5'-monophosphate. This gene is up-regulated in some neoplasms, suggesting it may play a role in malignant transformation. [provided by RefSeq, Jul 2008]","start":49024325,"end":49029408,"strand":-1,"description":"inosine monophosphate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:6053]"}, {"versioned_ensembl_gene_id":"ENSG00000236327.2","gene_symbol":"AL831737.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153890595,"end":153890865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223599.1","gene_symbol":"AL513523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153852106,"end":153853414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240068.1","gene_symbol":"RPL21P42","gene_name":"ribosomal protein L21 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:37017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271162","summary":null,"start":154023835,"end":154024298,"strand":1,"description":"ribosomal protein L21 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:37017]"}, {"versioned_ensembl_gene_id":"ENSG00000259273.1","gene_symbol":"AC027176.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89936492,"end":89937005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124224.16","gene_symbol":"PPP4R1L","gene_name":"protein phosphatase 4 regulatory subunit 1 like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15755]","synonyms":"PPP4R1P1,C20orf192,bA196N14.5,bA196N14.4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"55370","summary":null,"start":58228940,"end":58309439,"strand":-1,"description":"protein phosphatase 4 regulatory subunit 1 like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15755]"}, {"versioned_ensembl_gene_id":"ENSG00000229077.8","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31939669,"end":31955518,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000280377.1","gene_symbol":"AC027176.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89950760,"end":89951345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198837.9","gene_symbol":"DENND4B","gene_name":"DENN domain containing 4B [Source:HGNC Symbol;Acc:HGNC:29044]","synonyms":"KIAA0476","biotype":"protein_coding","ncbi_id":"9909","summary":null,"start":153929501,"end":153946696,"strand":-1,"description":"DENN domain containing 4B [Source:HGNC Symbol;Acc:HGNC:29044]"}, {"versioned_ensembl_gene_id":"ENSG00000283303.1","gene_symbol":"AC073869.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131363364,"end":131364881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233087.7","gene_symbol":"WTH3DI","gene_name":"RAB6C-like [Source:NCBI gene;Acc:150786]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150786","summary":null,"start":131361111,"end":131364142,"strand":-1,"description":"RAB6C-like [Source:NCBI gene;Acc:150786]"}, {"versioned_ensembl_gene_id":"ENSG00000125834.12","gene_symbol":"STK35","gene_name":"serine/threonine kinase 35 [Source:HGNC Symbol;Acc:HGNC:16254]","synonyms":"CLIK1,bA550O8.2","biotype":"protein_coding","ncbi_id":"140901","summary":"The protein encoded by this gene is a kinase that is predominantly found in the nucleus. However, it can interact with PDLIM1/CLP-36 in the cytoplasm and localize to actin stress fibers. The encoded protein may be a regulator of actin stress fibers in nonmuscle cells. [provided by RefSeq, Jul 2008]","start":2101611,"end":2177038,"strand":1,"description":"serine/threonine kinase 35 [Source:HGNC Symbol;Acc:HGNC:16254]"}, {"versioned_ensembl_gene_id":"ENSG00000133020.4","gene_symbol":"MYH8","gene_name":"myosin heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:7578]","synonyms":"MyHC-peri,MyHC-pn","biotype":"protein_coding","ncbi_id":"4626","summary":"Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is predominantly expressed in fetal skeletal muscle. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in trismus-pseudocamptodactyly syndrome. [provided by RefSeq, Sep 2009]","start":10390322,"end":10421950,"strand":-1,"description":"myosin heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:7578]"}, {"versioned_ensembl_gene_id":"ENSG00000204556.4","gene_symbol":"AL450124.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26018832,"end":26020684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170791.17","gene_symbol":"CHCHD7","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 7 [Source:HGNC Symbol;Acc:HGNC:28314]","synonyms":"MGC2217,COX23","biotype":"protein_coding","ncbi_id":"79145","summary":null,"start":56211686,"end":56218798,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 7 [Source:HGNC Symbol;Acc:HGNC:28314]"}, {"versioned_ensembl_gene_id":"ENSG00000275196.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54426396,"end":54427817,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000105939.12","gene_symbol":"ZC3HAV1","gene_name":"zinc finger CCCH-type containing, antiviral 1 [Source:HGNC Symbol;Acc:HGNC:23721]","synonyms":"ZC3HDC2,ZC3H2,ZAP,PARP13,MGC48898,FLJ13288,FLB6421","biotype":"protein_coding","ncbi_id":"56829","summary":"This gene encodes a CCCH-type zinc finger protein that is thought to prevent infection by retroviruses. Studies of the rat homolog indicate that the protein may primarily function to inhibit viral gene expression and induce an innate immunity to viral infection. Alternative splicing occurs at this locus and two variants, each encoding distinct isoforms, are described. [provided by RefSeq, Jul 2008]","start":139043520,"end":139109719,"strand":-1,"description":"zinc finger CCCH-type containing, antiviral 1 [Source:HGNC Symbol;Acc:HGNC:23721]"}, {"versioned_ensembl_gene_id":"ENSG00000233366.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"dJ111M5.3,ZNF463P","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28888832,"end":28889906,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000227840.1","gene_symbol":"KRTAP8-3P","gene_name":"keratin associated protein 8-3, pseudogene [Source:HGNC Symbol;Acc:HGNC:18949]","synonyms":"KRTAP8P2,KAP8B","biotype":"unprocessed_pseudogene","ncbi_id":"337981","summary":null,"start":30806932,"end":30807119,"strand":-1,"description":"keratin associated protein 8-3, pseudogene [Source:HGNC Symbol;Acc:HGNC:18949]"}, {"versioned_ensembl_gene_id":"ENSG00000183640.5","gene_symbol":"KRTAP8-1","gene_name":"keratin associated protein 8-1 [Source:HGNC Symbol;Acc:HGNC:18935]","synonyms":"KAP8.1","biotype":"protein_coding","ncbi_id":"337879","summary":null,"start":30812697,"end":30813252,"strand":-1,"description":"keratin associated protein 8-1 [Source:HGNC Symbol;Acc:HGNC:18935]"}, {"versioned_ensembl_gene_id":"ENSG00000148719.14","gene_symbol":"DNAJB12","gene_name":"DnaJ heat shock protein family (Hsp40) member B12 [Source:HGNC Symbol;Acc:HGNC:14891]","synonyms":"FLJ20027,DJ10","biotype":"protein_coding","ncbi_id":"54788","summary":"DNAJB12 belongs to the evolutionarily conserved DNAJ/HSP40 family of proteins, which regulate molecular chaperone activity by stimulating ATPase activity. DNAJ proteins may have up to 3 distinct domains: a conserved 70-amino acid J domain, usually at the N terminus; a glycine/phenylalanine (G/F)-rich region; and a cysteine-rich domain containing 4 motifs resembling a zinc finger domain (Ohtsuka and Hata, 2000 [PubMed 11147971]).[supplied by OMIM, Mar 2008]","start":72332830,"end":72355230,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B12 [Source:HGNC Symbol;Acc:HGNC:14891]"}, {"versioned_ensembl_gene_id":"ENSG00000159784.17","gene_symbol":"FAM131B","gene_name":"family with sequence similarity 131 member B [Source:HGNC Symbol;Acc:HGNC:22202]","synonyms":"KIAA0773","biotype":"protein_coding","ncbi_id":"9715","summary":null,"start":143353400,"end":143362770,"strand":-1,"description":"family with sequence similarity 131 member B [Source:HGNC Symbol;Acc:HGNC:22202]"}, {"versioned_ensembl_gene_id":"ENSG00000274749.1","gene_symbol":"KRTAP7-1","gene_name":"keratin associated protein 7-1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:18934]","synonyms":"KAP7.1","biotype":"protein_coding","ncbi_id":"337878","summary":null,"start":30829039,"end":30829759,"strand":-1,"description":"keratin associated protein 7-1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:18934]"}, {"versioned_ensembl_gene_id":"ENSG00000227368.1","gene_symbol":"CDK8P2","gene_name":"cyclin dependent kinase 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52296]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287419","summary":null,"start":112932625,"end":112933171,"strand":1,"description":"cyclin dependent kinase 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52296]"}, {"versioned_ensembl_gene_id":"ENSG00000240065.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32844136,"end":32859585,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000225080.1","gene_symbol":"PFN1P4","gene_name":"profilin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42992]","synonyms":"PFN1P5","biotype":"processed_pseudogene","ncbi_id":"767851","summary":null,"start":148129497,"end":148129898,"strand":1,"description":"profilin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42992]"}, {"versioned_ensembl_gene_id":"ENSG00000263956.6","gene_symbol":"NBPF11","gene_name":"NBPF member 11 [Source:HGNC Symbol;Acc:HGNC:31993]","synonyms":"NBPF24","biotype":"protein_coding","ncbi_id":"200030","summary":null,"start":148102046,"end":148152322,"strand":-1,"description":"NBPF member 11 [Source:HGNC Symbol;Acc:HGNC:31993]"}, {"versioned_ensembl_gene_id":"ENSG00000196937.10","gene_symbol":"FAM3C","gene_name":"family with sequence similarity 3 member C [Source:HGNC Symbol;Acc:HGNC:18664]","synonyms":"ILEI,GS3876","biotype":"protein_coding","ncbi_id":"10447","summary":"This gene is a member of the family with sequence similarity 3 (FAM3) family and encodes a secreted protein with a GG domain. A change in expression of this protein has been noted in pancreatic cancer-derived cells. [provided by RefSeq, Mar 2010]","start":121348851,"end":121396364,"strand":-1,"description":"family with sequence similarity 3 member C [Source:HGNC Symbol;Acc:HGNC:18664]"}, {"versioned_ensembl_gene_id":"ENSG00000237460.2","gene_symbol":"LINC01661","gene_name":"long intergenic non-protein coding RNA 1661 [Source:HGNC Symbol;Acc:HGNC:52449]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378889","summary":null,"start":106818239,"end":106838167,"strand":1,"description":"long intergenic non-protein coding RNA 1661 [Source:HGNC Symbol;Acc:HGNC:52449]"}, {"versioned_ensembl_gene_id":"ENSG00000226542.1","gene_symbol":"AC114814.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235084822,"end":235088586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172466.15","gene_symbol":"ZNF24","gene_name":"zinc finger protein 24 [Source:HGNC Symbol;Acc:HGNC:13032]","synonyms":"ZNF191,Zfp191,KOX17,ZSCAN3","biotype":"protein_coding","ncbi_id":"7572","summary":null,"start":35332212,"end":35345482,"strand":-1,"description":"zinc finger protein 24 [Source:HGNC Symbol;Acc:HGNC:13032]"}, {"versioned_ensembl_gene_id":"ENSG00000183862.5","gene_symbol":"CNGA2","gene_name":"cyclic nucleotide gated channel alpha 2 [Source:HGNC Symbol;Acc:HGNC:2149]","synonyms":"OCNCALPHA,OCNCa,OCNC1,FLJ46312,CNG2,CNCA1,CNCA","biotype":"protein_coding","ncbi_id":"1260","summary":"The protein encoded by this gene represents the alpha subunit of a cyclic nucleotide-gated olfactory channel. The encoded protein contains a carboxy-terminal leucine zipper that mediates channel formation. [provided by RefSeq, Jan 2010]","start":151738451,"end":151745304,"strand":1,"description":"cyclic nucleotide gated channel alpha 2 [Source:HGNC Symbol;Acc:HGNC:2149]"}, {"versioned_ensembl_gene_id":"ENSG00000253317.1","gene_symbol":"AC078906.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72196334,"end":72202269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198890.7","gene_symbol":"PRMT6","gene_name":"protein arginine methyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18241]","synonyms":"FLJ10559,HRMT1L6","biotype":"protein_coding","ncbi_id":"55170","summary":"The protein encoded by this gene belongs to the arginine N-methyltransferase family, which catalyze the sequential transfer of methyl group from S-adenosyl-L-methionine to the side chain nitrogens of arginine residues within proteins, to form methylated arginine derivatives and S-adenosyl-L-homocysteine. This protein can catalyze both, the formation of omega-N monomethylarginine and asymmetrical dimethylarginine, with a strong preference for the latter. It specifically mediates the asymmetric dimethylation of Arg2 of histone H3, and the methylated form represents a specific tag for epigenetic transcriptional repression. This protein also forms a complex with, and methylates DNA polymerase beta, resulting in stimulation of polymerase activity by enhancing DNA binding and processivity. [provided by RefSeq, Sep 2011]","start":107056679,"end":107059294,"strand":1,"description":"protein arginine methyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:18241]"}, {"versioned_ensembl_gene_id":"ENSG00000232517.2","gene_symbol":"AC112198.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":54808210,"end":54872551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224639.1","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"CO4,C4B3,CH,C4B1,CPAMD3,C4F","biotype":"processed_transcript","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":32058468,"end":32058494,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000226810.3","gene_symbol":"AC112198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54857272,"end":54858491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231032.1","gene_symbol":"AC114814.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235147016,"end":235147500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235293.1","gene_symbol":"AC114814.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235177896,"end":235178905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250229.1","gene_symbol":"AC111193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113840050,"end":113840236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257761.1","gene_symbol":"AC078860.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71582293,"end":71583852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278013.1","gene_symbol":"AC245033.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82540870,"end":82562374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230737.1","gene_symbol":"AC106870.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29890371,"end":29892354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175183.9","gene_symbol":"CSRP2","gene_name":"cysteine and glycine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:2470]","synonyms":"SmLIM,LMO5,CRP2","biotype":"protein_coding","ncbi_id":"1466","summary":"CSRP2 is a member of the CSRP family of genes, encoding a group of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. CRP2 contains two copies of the cysteine-rich amino acid sequence motif (LIM) with putative zinc-binding activity, and may be involved in regulating ordered cell growth. Other genes in the family include CSRP1 and CSRP3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":76858715,"end":76879060,"strand":-1,"description":"cysteine and glycine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:2470]"}, {"versioned_ensembl_gene_id":"ENSG00000230202.1","gene_symbol":"AL450405.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117998975,"end":117999448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196376.10","gene_symbol":"SLC35F1","gene_name":"solute carrier family 35 member F1 [Source:HGNC Symbol;Acc:HGNC:21483]","synonyms":"dJ230I3.1,C6orf169","biotype":"protein_coding","ncbi_id":"222553","summary":null,"start":117907526,"end":118317676,"strand":1,"description":"solute carrier family 35 member F1 [Source:HGNC Symbol;Acc:HGNC:21483]"}, {"versioned_ensembl_gene_id":"ENSG00000260836.1","gene_symbol":"AC245033.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":82540032,"end":82555932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149932.16","gene_symbol":"TMEM219","gene_name":"transmembrane protein 219 [Source:HGNC Symbol;Acc:HGNC:25201]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124446","summary":null,"start":29940885,"end":29973052,"strand":1,"description":"transmembrane protein 219 [Source:HGNC Symbol;Acc:HGNC:25201]"}, {"versioned_ensembl_gene_id":"ENSG00000280810.1","gene_symbol":"AC217769.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45573716,"end":45688015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254088.1","gene_symbol":"SLC2A3P4","gene_name":"solute carrier family 2 member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399495","summary":null,"start":86503591,"end":86505061,"strand":1,"description":"solute carrier family 2 member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31076]"}, {"versioned_ensembl_gene_id":"ENSG00000259707.1","gene_symbol":"AC105339.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82691723,"end":82692358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250569.1","gene_symbol":"NTAN1P2","gene_name":"N-terminal asparagine amidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45262]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420307","summary":null,"start":86481754,"end":86483002,"strand":-1,"description":"N-terminal asparagine amidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45262]"}, {"versioned_ensembl_gene_id":"ENSG00000254231.1","gene_symbol":"AC103760.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":86333274,"end":86343314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182774.10","gene_symbol":"RPS17","gene_name":"ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:10397]","synonyms":"MGC72007,S17,RPS17L2,RPS17L1,RPS17L","biotype":"protein_coding","ncbi_id":"6218","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S17E family of ribosomal proteins and is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia 4. Alternative splicing of this gene results in multiple transcript variants. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Apr 2014]","start":82536753,"end":82540564,"strand":-1,"description":"ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:10397]"}, {"versioned_ensembl_gene_id":"ENSG00000188707.5","gene_symbol":"ZBED6CL","gene_name":"ZBED6 C-terminal like [Source:HGNC Symbol;Acc:HGNC:21720]","synonyms":"C7orf29","biotype":"protein_coding","ncbi_id":"113763","summary":null,"start":150329789,"end":150332721,"strand":1,"description":"ZBED6 C-terminal like [Source:HGNC Symbol;Acc:HGNC:21720]"}, {"versioned_ensembl_gene_id":"ENSG00000259192.1","gene_symbol":"AC109631.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38458760,"end":38459540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176623.11","gene_symbol":"RMDN1","gene_name":"regulator of microtubule dynamics 1 [Source:HGNC Symbol;Acc:HGNC:24285]","synonyms":"RMD1,FLJ20665,FAM82B,CGI-90","biotype":"protein_coding","ncbi_id":"51115","summary":null,"start":86468257,"end":86514357,"strand":-1,"description":"regulator of microtubule dynamics 1 [Source:HGNC Symbol;Acc:HGNC:24285]"}, {"versioned_ensembl_gene_id":"ENSG00000106526.10","gene_symbol":"ACTR3C","gene_name":"ARP3 actin related protein 3 homolog C [Source:HGNC Symbol;Acc:HGNC:37282]","synonyms":"ARP11","biotype":"protein_coding","ncbi_id":"653857","summary":null,"start":150243916,"end":150323725,"strand":-1,"description":"ARP3 actin related protein 3 homolog C [Source:HGNC Symbol;Acc:HGNC:37282]"}, {"versioned_ensembl_gene_id":"ENSG00000154258.16","gene_symbol":"ABCA9","gene_name":"ATP binding cassette subfamily A member 9 [Source:HGNC Symbol;Acc:HGNC:39]","synonyms":"EST640918","biotype":"protein_coding","ncbi_id":"10350","summary":"This gene is a member of the superfamily of ATP-binding cassette (ABC) transporters and the encoded protein contains two transmembrane domains and two nucleotide binding folds. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This gene is a member of the ABC1 subfamily and is clustered with four other ABC1 family members on chromosome 17q24. Transcriptional expression of this gene is induced during monocyte differentiation into macrophages and is suppressed by cholesterol import. [provided by RefSeq, Jul 2008]","start":68974488,"end":69061064,"strand":-1,"description":"ATP binding cassette subfamily A member 9 [Source:HGNC Symbol;Acc:HGNC:39]"}, {"versioned_ensembl_gene_id":"ENSG00000276912.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54429845,"end":54441468,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000261722.1","gene_symbol":"AC092376.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79212711,"end":79229453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231827.3","gene_symbol":"AL513523.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153793947,"end":153802091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171262.11","gene_symbol":"FAM98B","gene_name":"family with sequence similarity 98 member B [Source:HGNC Symbol;Acc:HGNC:26773]","synonyms":"FLJ38426","biotype":"protein_coding","ncbi_id":"283742","summary":null,"start":38454127,"end":38487710,"strand":1,"description":"family with sequence similarity 98 member B [Source:HGNC Symbol;Acc:HGNC:26773]"}, {"versioned_ensembl_gene_id":"ENSG00000261472.1","gene_symbol":"AC084064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79505603,"end":79516293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227181.1","gene_symbol":"LINC01688","gene_name":"long intergenic non-protein coding RNA 1688 [Source:HGNC Symbol;Acc:HGNC:52475]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371644","summary":null,"start":182712862,"end":182714544,"strand":1,"description":"long intergenic non-protein coding RNA 1688 [Source:HGNC Symbol;Acc:HGNC:52475]"}, {"versioned_ensembl_gene_id":"ENSG00000204261.8","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"lincRNA","ncbi_id":"100507463","summary":null,"start":32844086,"end":32846495,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000136688.10","gene_symbol":"IL36G","gene_name":"interleukin 36, gamma [Source:HGNC Symbol;Acc:HGNC:15741]","synonyms":"IL1F9,IL1E,IL-1RP2,IL-1H1,IL-1F9,IL1H1","biotype":"protein_coding","ncbi_id":"56300","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. The activity of this cytokine is mediated by interleukin 1 receptor-like 2 (IL1RL2/IL1R-rp2), and is specifically inhibited by interleukin 1 family, member 5 (IL1F5/IL-1 delta). Interferon-gamma, tumor necrosis factor-alpha and interleukin 1, beta (IL1B) are reported to stimulate the expression of this cytokine in keratinocytes. The expression of this cytokine in keratinocytes can also be induced by a contact hypersensitivity reaction or herpes simplex virus infection. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. [provided by RefSeq, May 2019]","start":112973203,"end":112985665,"strand":1,"description":"interleukin 36, gamma [Source:HGNC Symbol;Acc:HGNC:15741]"}, {"versioned_ensembl_gene_id":"ENSG00000229207.1","gene_symbol":"SERPINH1P1","gene_name":"serpin family H member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19917]","synonyms":"SERPINHP1,pshsp47,bA571F15.6","biotype":"processed_pseudogene","ncbi_id":"158172","summary":null,"start":34318407,"end":34319655,"strand":1,"description":"serpin family H member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19917]"}, {"versioned_ensembl_gene_id":"ENSG00000143614.9","gene_symbol":"GATAD2B","gene_name":"GATA zinc finger domain containing 2B [Source:HGNC Symbol;Acc:HGNC:30778]","synonyms":"P66beta","biotype":"protein_coding","ncbi_id":"57459","summary":"This gene encodes a zinc finger protein transcriptional repressor. The encoded protein is part of the methyl-CpG-binding protein-1 complex, which represses gene expression by deacetylating methylated nucleosomes. Mutations in this gene are linked to intellectual disability and dysmorphic features associated with cognitive disability. [provided by RefSeq, Jun 2016]","start":153789030,"end":153923360,"strand":-1,"description":"GATA zinc finger domain containing 2B [Source:HGNC Symbol;Acc:HGNC:30778]"}, {"versioned_ensembl_gene_id":"ENSG00000187522.14","gene_symbol":"HSPA14","gene_name":"heat shock protein family A (Hsp70) member 14 [Source:HGNC Symbol;Acc:HGNC:29526]","synonyms":"HSP70L1,HSP70-4","biotype":"protein_coding","ncbi_id":"51182","summary":null,"start":14838164,"end":14871741,"strand":1,"description":"heat shock protein family A (Hsp70) member 14 [Source:HGNC Symbol;Acc:HGNC:29526]"}, {"versioned_ensembl_gene_id":"ENSG00000180773.14","gene_symbol":"SLC36A4","gene_name":"solute carrier family 36 member 4 [Source:HGNC Symbol;Acc:HGNC:19660]","synonyms":"PAT4,FLJ38932","biotype":"protein_coding","ncbi_id":"120103","summary":"SLC36A4 belongs to the SLC36 family of amino acid transporters based on sequence similarity with other family members (e.g., SLC36A1; MIM 606561). SLC36 proteins contain about 500 amino acids and have 9 to 11 transmembrane domains. Unlike other SLC36 family members, which are proton-coupled amino acid transporters, SLC36A4 is a high-affinity/low-capacity non-proton-coupled amino acid transporter (Pillai and Meredith, 2011 [PubMed 21097500]).[supplied by OMIM, Feb 2011]","start":93144171,"end":93197964,"strand":-1,"description":"solute carrier family 36 member 4 [Source:HGNC Symbol;Acc:HGNC:19660]"}, {"versioned_ensembl_gene_id":"ENSG00000183770.5","gene_symbol":"FOXL2","gene_name":"forkhead box L2 [Source:HGNC Symbol;Acc:HGNC:1092]","synonyms":"BPES1,BPES","biotype":"protein_coding","ncbi_id":"668","summary":"This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016]","start":138944224,"end":138947140,"strand":-1,"description":"forkhead box L2 [Source:HGNC Symbol;Acc:HGNC:1092]"}, {"versioned_ensembl_gene_id":"ENSG00000101115.12","gene_symbol":"SALL4","gene_name":"spalt like transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:15924]","synonyms":"ZNF797,dJ1112F19.1","biotype":"protein_coding","ncbi_id":"57167","summary":"This gene encodes a zinc finger transcription factor thought to play a role in the development of abducens motor neurons. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":51782331,"end":51802520,"strand":-1,"description":"spalt like transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:15924]"}, {"versioned_ensembl_gene_id":"ENSG00000244733.5","gene_symbol":"AL132656.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79660891,"end":79677996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148300.11","gene_symbol":"REXO4","gene_name":"REX4 homolog, 3'-5' exonuclease [Source:HGNC Symbol;Acc:HGNC:12820]","synonyms":"XPMC2H,hPMC2","biotype":"protein_coding","ncbi_id":"57109","summary":null,"start":133406059,"end":133418096,"strand":-1,"description":"REX4 homolog, 3'-5' exonuclease [Source:HGNC Symbol;Acc:HGNC:12820]"}, {"versioned_ensembl_gene_id":"ENSG00000271488.1","gene_symbol":"RBM11P1","gene_name":"RNA binding motif protein 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420213","summary":null,"start":132764660,"end":132765458,"strand":1,"description":"RNA binding motif protein 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43743]"}, {"versioned_ensembl_gene_id":"ENSG00000233632.1","gene_symbol":"Z82198.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33137140,"end":33137338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253754.1","gene_symbol":"AC087620.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108226200,"end":108227544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184961.5","gene_symbol":"RPL7AP49","gene_name":"ribosomal protein L7a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35507]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271214","summary":null,"start":39983821,"end":39984401,"strand":-1,"description":"ribosomal protein L7a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35507]"}, {"versioned_ensembl_gene_id":"ENSG00000124208.16","gene_symbol":"TMEM189-UBE2V1","gene_name":"TMEM189-UBE2V1 readthrough [Source:HGNC Symbol;Acc:HGNC:33521]","synonyms":"Kua-UEV,CROC-1B","biotype":"protein_coding","ncbi_id":"387522","summary":"The TMEM189-UEV mRNA is an infrequent but naturally occurring read-through transcript of the neighboring TMEM189 and UBE2V1 genes. Ubiquitin-conjugating E2 enzyme variant proteins constitute a distinct subfamily within the E2 protein family. They have sequence similarity to other ubiquitin-conjugating enzymes but lack the conserved cysteine residue that is critical for the catalytic activity of E2s. The protein produced by this transcript has UEV1 B domains but the protein is localized to the cytoplasm rather than to the nucleus. The significance of this read-through mRNA and the function of its protein product has not yet been determined. [provided by RefSeq, Oct 2010]","start":50081124,"end":50153637,"strand":-1,"description":"TMEM189-UBE2V1 readthrough [Source:HGNC Symbol;Acc:HGNC:33521]"}, {"versioned_ensembl_gene_id":"ENSG00000284634.1","gene_symbol":"AC092821.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9448295,"end":9658392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076043.9","gene_symbol":"REXO2","gene_name":"RNA exonuclease 2 [Source:HGNC Symbol;Acc:HGNC:17851]","synonyms":"SFN,DKFZP566E144,CGI-114","biotype":"protein_coding","ncbi_id":"25996","summary":"This gene encodes a 3'-to-5' exonuclease specific for small (primarily 5 nucleotides or less in length) single-stranded RNA and DNA oligomers. This protein may have a role in DNA repair, replication, and recombination, and in RNA processing and degradation. It may also be involved in resistance of human cells to UV-C-induced cell death through its role in the DNA repair process. [provided by RefSeq, Nov 2011]","start":114439386,"end":114450279,"strand":1,"description":"RNA exonuclease 2 [Source:HGNC Symbol;Acc:HGNC:17851]"}, {"versioned_ensembl_gene_id":"ENSG00000174516.14","gene_symbol":"PELI3","gene_name":"pellino E3 ubiquitin protein ligase family member 3 [Source:HGNC Symbol;Acc:HGNC:30010]","synonyms":"MGC35521","biotype":"protein_coding","ncbi_id":"246330","summary":"The protein encoded by this gene is a scaffold protein and an intermediate signaling protein in the innate immune response pathway. The encoded protein helps transmit the immune response signal from Toll-like receptors to IRAK1/TRAF6 complexes. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]","start":66466327,"end":66477337,"strand":1,"description":"pellino E3 ubiquitin protein ligase family member 3 [Source:HGNC Symbol;Acc:HGNC:30010]"}, {"versioned_ensembl_gene_id":"ENSG00000259259.1","gene_symbol":"NPM1P42","gene_name":"nucleophosmin 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:45221]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729686","summary":null,"start":72899399,"end":72900260,"strand":-1,"description":"nucleophosmin 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:45221]"}, {"versioned_ensembl_gene_id":"ENSG00000181408.3","gene_symbol":"UTS2R","gene_name":"urotensin 2 receptor [Source:HGNC Symbol;Acc:HGNC:4468]","synonyms":"GPR14","biotype":"protein_coding","ncbi_id":"2837","summary":null,"start":82374230,"end":82375586,"strand":1,"description":"urotensin 2 receptor [Source:HGNC Symbol;Acc:HGNC:4468]"}, {"versioned_ensembl_gene_id":"ENSG00000278964.1","gene_symbol":"AC132938.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82362349,"end":82363196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070540.12","gene_symbol":"WIPI1","gene_name":"WD repeat domain, phosphoinositide interacting 1 [Source:HGNC Symbol;Acc:HGNC:25471]","synonyms":"WIPI49,FLJ10055,ATG18A,ATG18","biotype":"protein_coding","ncbi_id":"55062","summary":"This gene encodes a WD40 repeat protein. Members of the WD40 repeat family are key components of many essential biologic functions. They regulate the assembly of multiprotein complexes by presenting a beta-propeller platform for simultaneous and reversible protein-protein interactions. Members of the WIPI subfamily of WD40 repeat proteins have a 7-bladed propeller structure and contain a conserved motif for interaction with phospholipids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":68420948,"end":68457513,"strand":-1,"description":"WD repeat domain, phosphoinositide interacting 1 [Source:HGNC Symbol;Acc:HGNC:25471]"}, {"versioned_ensembl_gene_id":"ENSG00000204604.9","gene_symbol":"ZNF468","gene_name":"zinc finger protein 468 [Source:HGNC Symbol;Acc:HGNC:33105]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90333","summary":null,"start":52838008,"end":52857649,"strand":-1,"description":"zinc finger protein 468 [Source:HGNC Symbol;Acc:HGNC:33105]"}, {"versioned_ensembl_gene_id":"ENSG00000257156.1","gene_symbol":"AC024909.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89048187,"end":89309553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234886.1","gene_symbol":"MTND5P26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42295]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873268","summary":null,"start":102803041,"end":102806138,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42295]"}, {"versioned_ensembl_gene_id":"ENSG00000069812.11","gene_symbol":"HES2","gene_name":"hes family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:16005]","synonyms":"bHLHb40","biotype":"protein_coding","ncbi_id":"54626","summary":null,"start":6412418,"end":6424670,"strand":-1,"description":"hes family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:16005]"}, {"versioned_ensembl_gene_id":"ENSG00000226056.1","gene_symbol":"MTND4P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42219]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873253","summary":null,"start":102799942,"end":102801399,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42219]"}, {"versioned_ensembl_gene_id":"ENSG00000273118.1","gene_symbol":"AC093865.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":212581357,"end":213021545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274108.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738481,"end":54752986,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000228194.1","gene_symbol":"Z83846.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33014980,"end":33015461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197083.11","gene_symbol":"ZNF300P1","gene_name":"zinc finger protein 300 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27032]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"134466","summary":null,"start":150930645,"end":150946289,"strand":-1,"description":"zinc finger protein 300 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27032]"}, {"versioned_ensembl_gene_id":"ENSG00000229673.1","gene_symbol":"Z73495.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32783177,"end":32784982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136098.16","gene_symbol":"NEK3","gene_name":"NIMA related kinase 3 [Source:HGNC Symbol;Acc:HGNC:7746]","synonyms":"MGC29949,HSPK36","biotype":"protein_coding","ncbi_id":"4752","summary":"This gene encodes a member of the NimA (never in mitosis A) family of serine/threonine protein kinases. The encoded protein differs from other NimA family members in that it is not cell cycle regulated and is found primarily in the cytoplasm. The kinase is activated by prolactin stimulation, leading to phosphorylation of VAV2 guanine nucleotide exchange factor, paxillin, and activation of the RAC1 GTPase. Two functional alleles for this gene have been identified in humans. The reference genome assembly (GRCh38) represents a functional allele that is associated with the inclusion of an additional coding exon in protein-coding transcripts, compared to an alternate functional allele that lacks the exon. [provided by RefSeq, Sep 2019]","start":52132639,"end":52159861,"strand":-1,"description":"NIMA related kinase 3 [Source:HGNC Symbol;Acc:HGNC:7746]"}, {"versioned_ensembl_gene_id":"ENSG00000277392.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736494,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000106436.4","gene_symbol":"MYL10","gene_name":"myosin light chain 10 [Source:HGNC Symbol;Acc:HGNC:29825]","synonyms":"PLRLC,MYLC2PL,MGC3479","biotype":"protein_coding","ncbi_id":"93408","summary":null,"start":101613325,"end":101629296,"strand":-1,"description":"myosin light chain 10 [Source:HGNC Symbol;Acc:HGNC:29825]"}, {"versioned_ensembl_gene_id":"ENSG00000276386.1","gene_symbol":"CNTNAP3P2","gene_name":"contactin associated protein-like 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49589]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643827","summary":null,"start":67059560,"end":67293468,"strand":1,"description":"contactin associated protein-like 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49589]"}, {"versioned_ensembl_gene_id":"ENSG00000265100.1","gene_symbol":"AC005332.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68246629,"end":68247938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232549.1","gene_symbol":"SRD5A1P1","gene_name":"steroid 5 alpha-reductase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11286]","synonyms":"SRD5AP1","biotype":"processed_pseudogene","ncbi_id":"6719","summary":null,"start":139446891,"end":139447676,"strand":1,"description":"steroid 5 alpha-reductase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11286]"}, {"versioned_ensembl_gene_id":"ENSG00000164953.15","gene_symbol":"TMEM67","gene_name":"transmembrane protein 67 [Source:HGNC Symbol;Acc:HGNC:28396]","synonyms":"MGC26979,JBTS6,NPHP11,MKS3","biotype":"protein_coding","ncbi_id":"91147","summary":"The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]","start":93754844,"end":93819234,"strand":1,"description":"transmembrane protein 67 [Source:HGNC Symbol;Acc:HGNC:28396]"}, {"versioned_ensembl_gene_id":"ENSG00000145692.14","gene_symbol":"BHMT","gene_name":"betaine--homocysteine S-methyltransferase [Source:HGNC Symbol;Acc:HGNC:1047]","synonyms":"BHMT1","biotype":"protein_coding","ncbi_id":"635","summary":"This gene encodes a cytosolic enzyme that catalyzes the conversion of betaine and homocysteine to dimethylglycine and methionine, respectively. Defects in this gene could lead to hyperhomocyst(e)inemia, but such a defect has not yet been observed. [provided by RefSeq, Jul 2008]","start":79111779,"end":79132290,"strand":1,"description":"betaine--homocysteine S-methyltransferase [Source:HGNC Symbol;Acc:HGNC:1047]"}, {"versioned_ensembl_gene_id":"ENSG00000230922.1","gene_symbol":"AL079301.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45000565,"end":45003619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223842.1","gene_symbol":"AL360093.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219222248,"end":219225497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206208.11","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33470037,"end":33484728,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000254617.1","gene_symbol":"AP005435.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89887366,"end":89889991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171634.16","gene_symbol":"BPTF","gene_name":"bromodomain PHD finger transcription factor [Source:HGNC Symbol;Acc:HGNC:3581]","synonyms":"NURF301,FALZ,FAC1","biotype":"protein_coding","ncbi_id":"2186","summary":"This gene was identified by the reactivity of its encoded protein to a monoclonal antibody prepared against brain homogenates from patients with Alzheimer's disease. Analysis of the original protein (fetal Alz-50 reactive clone 1, or FAC1), identified as an 810 aa protein containing a DNA-binding domain and a zinc finger motif, suggested it might play a role in the regulation of transcription. High levels of FAC1 were detected in fetal brain and in patients with neurodegenerative diseases. The protein encoded by this gene is actually much larger than originally thought, and it also contains a C-terminal bromodomain characteristic of proteins that regulate transcription during proliferation. The encoded protein is highly similar to the largest subunit of the Drosophila NURF (nucleosome remodeling factor) complex. In Drosophila, the NURF complex, which catalyzes nucleosome sliding on DNA and interacts with sequence-specific transcription factors, is necessary for the chromatin remodeling required for transcription. Two alternative transcripts encoding different isoforms have been described completely. [provided by RefSeq, Jul 2008]","start":67825524,"end":67984378,"strand":1,"description":"bromodomain PHD finger transcription factor [Source:HGNC Symbol;Acc:HGNC:3581]"}, {"versioned_ensembl_gene_id":"ENSG00000261055.1","gene_symbol":"AL450468.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109895973,"end":109897861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259532.1","gene_symbol":"AC009269.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70748932,"end":70754177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269836.1","gene_symbol":"AC020913.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17177511,"end":17178476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270818.1","gene_symbol":"AL445675.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242882066,"end":242883475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258987.1","gene_symbol":"AL132642.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93939555,"end":93944129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102935.11","gene_symbol":"ZNF423","gene_name":"zinc finger protein 423 [Source:HGNC Symbol;Acc:HGNC:16762]","synonyms":"Zfp104,Roaz,OAZ,NPHP14,KIAA0760,JBTS19,Ebfaz","biotype":"protein_coding","ncbi_id":"23090","summary":"The protein encoded by this gene is a nuclear protein that belongs to the family of Kruppel-like C2H2 zinc finger proteins. It functions as a DNA-binding transcription factor by using distinct zinc fingers in different signaling pathways. Thus, it is thought that this gene may have multiple roles in signal transduction during development. Mutations in this gene are associated with nephronophthisis-14 and Joubert syndrome-19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2012]","start":49487524,"end":49857919,"strand":-1,"description":"zinc finger protein 423 [Source:HGNC Symbol;Acc:HGNC:16762]"}, {"versioned_ensembl_gene_id":"ENSG00000242107.2","gene_symbol":"LINC01100","gene_name":"long intergenic non-protein coding RNA 1100 [Source:HGNC Symbol;Acc:HGNC:49224]","synonyms":null,"biotype":"lincRNA","ncbi_id":"730109","summary":null,"start":160016024,"end":160031423,"strand":1,"description":"long intergenic non-protein coding RNA 1100 [Source:HGNC Symbol;Acc:HGNC:49224]"}, {"versioned_ensembl_gene_id":"ENSG00000280430.1","gene_symbol":"AP002782.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90731110,"end":90731723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265936.1","gene_symbol":"AC091042.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67375133,"end":67375305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240621.1","gene_symbol":"OR2AO1P","gene_name":"olfactory receptor family 2 subfamily AO member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403235","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144176740,"end":144177142,"strand":1,"description":"olfactory receptor family 2 subfamily AO member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31247]"}, {"versioned_ensembl_gene_id":"ENSG00000242670.1","gene_symbol":"RPL22P13","gene_name":"ribosomal protein L22 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442108","summary":null,"start":54221126,"end":54221472,"strand":1,"description":"ribosomal protein L22 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36352]"}, {"versioned_ensembl_gene_id":"ENSG00000221858.3","gene_symbol":"OR2A12","gene_name":"olfactory receptor family 2 subfamily A member 12 [Source:HGNC Symbol;Acc:HGNC:15082]","synonyms":"OR2A12P","biotype":"protein_coding","ncbi_id":"346525","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144086278,"end":144098953,"strand":1,"description":"olfactory receptor family 2 subfamily A member 12 [Source:HGNC Symbol;Acc:HGNC:15082]"}, {"versioned_ensembl_gene_id":"ENSG00000099889.13","gene_symbol":"ARVCF","gene_name":"armadillo repeat gene deleted in velocardiofacial syndrome [Source:HGNC Symbol;Acc:HGNC:728]","synonyms":null,"biotype":"protein_coding","ncbi_id":"421","summary":"Armadillo Repeat gene deleted in Velo-Cardio-Facial syndrome (ARVCF) is a member of the catenin family. This family plays an important role in the formation of adherens junction complexes, which are thought to facilitate communication between the inside and outside environments of a cell. The ARVCF gene was isolated in the search for the genetic defect responsible for the autosomal dominant Velo-Cardio-Facial syndrome (VCFS), a relatively common human disorder with phenotypic features including cleft palate, conotruncal heart defects and facial dysmorphology. The ARVCF gene encodes a protein containing two motifs, a coiled coil domain in the N-terminus and a 10 armadillo repeat sequence in the midregion. Since these sequences can facilitate protein-protein interactions ARVCF is thought to function in a protein complex. In addition, ARVCF contains a predicted nuclear-targeting sequence suggesting that it may have a function as a nuclear protein. [provided by RefSeq, Jun 2010]","start":19969896,"end":20016808,"strand":-1,"description":"armadillo repeat gene deleted in velocardiofacial syndrome [Source:HGNC Symbol;Acc:HGNC:728]"}, {"versioned_ensembl_gene_id":"ENSG00000106333.12","gene_symbol":"PCOLCE","gene_name":"procollagen C-endopeptidase enhancer [Source:HGNC Symbol;Acc:HGNC:8738]","synonyms":"PCPE1,PCPE","biotype":"protein_coding","ncbi_id":"5118","summary":"Fibrillar collagen types I-III are synthesized as precursor molecules known as procollagens. These precursors contain amino- and carboxyl-terminal peptide extensions known as N- and C-propeptides, respectively, which are cleaved, upon secretion of procollagen from the cell, to yield the mature triple helical, highly structured fibrils. This gene encodes a glycoprotein which binds and drives the enzymatic cleavage of type I procollagen and heightens C-proteinase activity. [provided by RefSeq, Jul 2008]","start":100602177,"end":100608175,"strand":1,"description":"procollagen C-endopeptidase enhancer [Source:HGNC Symbol;Acc:HGNC:8738]"}, {"versioned_ensembl_gene_id":"ENSG00000270969.1","gene_symbol":"AP001823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107585901,"end":107586903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279251.1","gene_symbol":"AC015726.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19855747,"end":19856164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105552.14","gene_symbol":"BCAT2","gene_name":"branched chain amino acid transaminase 2 [Source:HGNC Symbol;Acc:HGNC:977]","synonyms":"BCT2,BCAM","biotype":"protein_coding","ncbi_id":"587","summary":"This gene encodes a branched chain aminotransferase found in mitochondria. The encoded protein forms a dimer that catalyzes the first step in the production of the branched chain amino acids leucine, isoleucine, and valine. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":48795062,"end":48811029,"strand":-1,"description":"branched chain amino acid transaminase 2 [Source:HGNC Symbol;Acc:HGNC:977]"}, {"versioned_ensembl_gene_id":"ENSG00000214904.5","gene_symbol":"DUTP8","gene_name":"deoxyuridine triphosphatase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39521]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873914","summary":null,"start":98048555,"end":98049043,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39521]"}, {"versioned_ensembl_gene_id":"ENSG00000272006.1","gene_symbol":"AC037487.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64951498,"end":64951609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272346.2","gene_symbol":"AC103810.9","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64940606,"end":64940717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265912.1","gene_symbol":"AC037487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64943262,"end":64951054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280299.1","gene_symbol":"AC037487.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":64940602,"end":64954177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254428.1","gene_symbol":"AP003392.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119003742,"end":119004893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266155.2","gene_symbol":"AC103810.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64936485,"end":64940229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138074.14","gene_symbol":"SLC5A6","gene_name":"solute carrier family 5 member 6 [Source:HGNC Symbol;Acc:HGNC:11041]","synonyms":"SMVT","biotype":"protein_coding","ncbi_id":"8884","summary":null,"start":27199587,"end":27212958,"strand":-1,"description":"solute carrier family 5 member 6 [Source:HGNC Symbol;Acc:HGNC:11041]"}, {"versioned_ensembl_gene_id":"ENSG00000242197.2","gene_symbol":"AC098869.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40491733,"end":40492024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197555.9","gene_symbol":"SIPA1L1","gene_name":"signal induced proliferation associated 1 like 1 [Source:HGNC Symbol;Acc:HGNC:20284]","synonyms":"KIAA0440,E6TP1","biotype":"protein_coding","ncbi_id":"26037","summary":null,"start":71320449,"end":71741229,"strand":1,"description":"signal induced proliferation associated 1 like 1 [Source:HGNC Symbol;Acc:HGNC:20284]"}, {"versioned_ensembl_gene_id":"ENSG00000271234.1","gene_symbol":"AL078605.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170297876,"end":170298375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268093.1","gene_symbol":"AC022154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48619272,"end":48624132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237296.9","gene_symbol":"SMG1P1","gene_name":"SMG1P1, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44186]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"641298","summary":null,"start":22437008,"end":22492220,"strand":1,"description":"SMG1P1, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44186]"}, {"versioned_ensembl_gene_id":"ENSG00000254823.1","gene_symbol":"AP001782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123313674,"end":123314770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164530.13","gene_symbol":"PI16","gene_name":"peptidase inhibitor 16 [Source:HGNC Symbol;Acc:HGNC:21245]","synonyms":"MSMBBP,MGC45378,dJ90K10.5,CD364","biotype":"protein_coding","ncbi_id":"221476","summary":null,"start":36948263,"end":36964837,"strand":1,"description":"peptidase inhibitor 16 [Source:HGNC Symbol;Acc:HGNC:21245]"}, {"versioned_ensembl_gene_id":"ENSG00000255342.1","gene_symbol":"AP000926.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123135923,"end":123136376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258747.1","gene_symbol":"AL356022.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44507407,"end":44538513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166925.8","gene_symbol":"TSC22D4","gene_name":"TSC22 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:21696]","synonyms":"TILZ2,THG-1","biotype":"protein_coding","ncbi_id":"81628","summary":"TSC22D4 is a member of the TSC22 domain family of leucine zipper transcriptional regulators (see TSC22D3; MIM 300506) (Kester et al., 1999 [PubMed 10488076]; Fiorenza et al., 2001 [PubMed 11707329]).[supplied by OMIM, Mar 2008]","start":100463359,"end":100479279,"strand":-1,"description":"TSC22 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:21696]"}, {"versioned_ensembl_gene_id":"ENSG00000275819.4","gene_symbol":"LAIR2","gene_name":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]","synonyms":"CD306","biotype":"protein_coding","ncbi_id":"3904","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1, a membrane-bound receptor that modulates innate immune response. The protein encoded by this locus is a soluble receptor that may play roles in both inhibition of collagen-induced platelet aggregation and vessel formation during placental implantation. This gene maps to a region of 19q13.4, termed the leukocyte receptor cluster, which contains 29 genes in the immunoglobulin superfamily. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":54428232,"end":54441459,"strand":1,"description":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]"}, {"versioned_ensembl_gene_id":"ENSG00000180198.15","gene_symbol":"RCC1","gene_name":"regulator of chromosome condensation 1 [Source:HGNC Symbol;Acc:HGNC:1913]","synonyms":"CHC1","biotype":"protein_coding","ncbi_id":"1104","summary":null,"start":28505943,"end":28539300,"strand":1,"description":"regulator of chromosome condensation 1 [Source:HGNC Symbol;Acc:HGNC:1913]"}, {"versioned_ensembl_gene_id":"ENSG00000271840.1","gene_symbol":"AL031281.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22100613,"end":22101360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233135.1","gene_symbol":"RPS27P18","gene_name":"ribosomal protein S27 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36296]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100271380","summary":null,"start":125473686,"end":125473932,"strand":-1,"description":"ribosomal protein S27 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36296]"}, {"versioned_ensembl_gene_id":"ENSG00000150459.12","gene_symbol":"SAP18","gene_name":"Sin3A associated protein 18 [Source:HGNC Symbol;Acc:HGNC:10530]","synonyms":"SAP18p,MGC27131,2HOR0202","biotype":"protein_coding","ncbi_id":"10284","summary":"Histone acetylation plays a key role in the regulation of eukaryotic gene expression. Histone acetylation and deacetylation are catalyzed by multisubunit complexes. The protein encoded by this gene is a component of the histone deacetylase complex, which includes SIN3, SAP30, HDAC1, HDAC2, RbAp46, RbAp48, and other polypeptides. This protein directly interacts with SIN3 and enhances SIN3-mediated transcriptional repression when tethered to the promoter. A pseudogene has been identified on chromosome 2. [provided by RefSeq, Dec 2008]","start":21140514,"end":21149084,"strand":1,"description":"Sin3A associated protein 18 [Source:HGNC Symbol;Acc:HGNC:10530]"}, {"versioned_ensembl_gene_id":"ENSG00000134612.11","gene_symbol":"FOLH1B","gene_name":"folate hydrolase 1B [Source:HGNC Symbol;Acc:HGNC:13636]","synonyms":"PSMAL,FOLHP,FOLH2","biotype":"transcribed_processed_pseudogene","ncbi_id":"219595","summary":null,"start":89639227,"end":89698718,"strand":1,"description":"folate hydrolase 1B [Source:HGNC Symbol;Acc:HGNC:13636]"}, {"versioned_ensembl_gene_id":"ENSG00000106714.17","gene_symbol":"CNTNAP3","gene_name":"contactin associated protein like 3 [Source:HGNC Symbol;Acc:HGNC:13834]","synonyms":"KIAA1714,FLJ14195,CNTNAP3A,CASPR3","biotype":"protein_coding","ncbi_id":"79937","summary":"The protein encoded by this gene belongs to the NCP family of cell-recognition molecules. This family represents a distinct subgroup of the neurexins. NCP proteins mediate neuron-glial interactions in vertebrates and glial-glial contact in invertebrates. The protein encoded by this gene may play a role in cell recognition within the nervous system. Alternatively spliced transcript variants encoding different isoforms have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":39072767,"end":39288315,"strand":-1,"description":"contactin associated protein like 3 [Source:HGNC Symbol;Acc:HGNC:13834]"}, {"versioned_ensembl_gene_id":"ENSG00000179912.20","gene_symbol":"R3HDM2","gene_name":"R3H domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29167]","synonyms":"KIAA1002","biotype":"protein_coding","ncbi_id":"22864","summary":null,"start":57253762,"end":57431005,"strand":-1,"description":"R3H domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29167]"}, {"versioned_ensembl_gene_id":"ENSG00000278977.1","gene_symbol":"AC003101.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31533171,"end":31533938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156521.13","gene_symbol":"TYSND1","gene_name":"trypsin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28531]","synonyms":"NET41,MGC34695","biotype":"protein_coding","ncbi_id":"219743","summary":"This gene encodes a protease that removes the N-terminal peroxisomal targeting signal (PTS2) from proteins produced in the cytosol, thereby facilitating their import into the peroxisome. The encoded protein is also capable of removing the C-terminal peroxisomal targeting signal (PTS1) from proteins in the peroxisomal matrix. The full-length protein undergoes self-cleavage to produce shorter, potentially inactive, peptides. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013]","start":70137981,"end":70146676,"strand":-1,"description":"trypsin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28531]"}, {"versioned_ensembl_gene_id":"ENSG00000106004.4","gene_symbol":"HOXA5","gene_name":"homeobox A5 [Source:HGNC Symbol;Acc:HGNC:5106]","synonyms":"HOX1C,HOX1","biotype":"protein_coding","ncbi_id":"3202","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Methylation of this gene may result in the loss of its expression and, since the encoded protein upregulates the tumor suppressor p53, this protein may play an important role in tumorigenesis. [provided by RefSeq, Jul 2008]","start":27141052,"end":27143668,"strand":-1,"description":"homeobox A5 [Source:HGNC Symbol;Acc:HGNC:5106]"}, {"versioned_ensembl_gene_id":"ENSG00000261371.5","gene_symbol":"PECAM1","gene_name":"platelet and endothelial cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:8823]","synonyms":"CD31","biotype":"protein_coding","ncbi_id":"5175","summary":"The protein encoded by this gene is found on the surface of platelets, monocytes, neutrophils, and some types of T-cells, and makes up a large portion of endothelial cell intercellular junctions. The encoded protein is a member of the immunoglobulin superfamily and is likely involved in leukocyte migration, angiogenesis, and integrin activation. [provided by RefSeq, May 2010]","start":64319415,"end":64413776,"strand":-1,"description":"platelet and endothelial cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:8823]"}, {"versioned_ensembl_gene_id":"ENSG00000264188.1","gene_symbol":"AC106037.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21661787,"end":21662395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268095.1","gene_symbol":"ZNF649-AS1","gene_name":"ZNF649 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51285]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928571","summary":null,"start":51888025,"end":51900463,"strand":1,"description":"ZNF649 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51285]"}, {"versioned_ensembl_gene_id":"ENSG00000084090.13","gene_symbol":"STARD7","gene_name":"StAR related lipid transfer domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18063]","synonyms":"GTT1","biotype":"protein_coding","ncbi_id":"56910","summary":null,"start":96184859,"end":96208825,"strand":-1,"description":"StAR related lipid transfer domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18063]"}, {"versioned_ensembl_gene_id":"ENSG00000234139.2","gene_symbol":"AL035420.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36072441,"end":36085260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258387.1","gene_symbol":"AL358913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43592142,"end":43592262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228873.1","gene_symbol":"AC012307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96145602,"end":96147012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230365.1","gene_symbol":"AL451129.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11275314,"end":11276314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154553.13","gene_symbol":"PDLIM3","gene_name":"PDZ and LIM domain 3 [Source:HGNC Symbol;Acc:HGNC:20767]","synonyms":"ALP","biotype":"protein_coding","ncbi_id":"27295","summary":"The protein encoded by this gene contains a PDZ domain and a LIM domain, indicating that it may be involved in cytoskeletal assembly. In support of this, the encoded protein has been shown to bind the spectrin-like repeats of alpha-actinin-2 and to colocalize with alpha-actinin-2 at the Z lines of skeletal muscle. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Aberrant alternative splicing of this gene may play a role in myotonic dystrophy. [provided by RefSeq, Apr 2012]","start":185500660,"end":185535612,"strand":-1,"description":"PDZ and LIM domain 3 [Source:HGNC Symbol;Acc:HGNC:20767]"}, {"versioned_ensembl_gene_id":"ENSG00000234690.6","gene_symbol":"AC106869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47192405,"end":47345074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238255.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30686326,"end":30687055,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000270605.1","gene_symbol":"AL353622.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28239509,"end":28241453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211838.1","gene_symbol":"TRAJ52","gene_name":"T-cell receptor alpha joining 52 [Source:HGNC Symbol;Acc:HGNC:12084]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28703","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22486228,"end":22486296,"strand":1,"description":"T-cell receptor alpha joining 52 [Source:HGNC Symbol;Acc:HGNC:12084]"}, {"versioned_ensembl_gene_id":"ENSG00000260033.1","gene_symbol":"AC023813.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48600176,"end":48600644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158164.6","gene_symbol":"TMSB15A","gene_name":"thymosin beta 15a [Source:HGNC Symbol;Acc:HGNC:30744]","synonyms":"TMSNB,TMSL8","biotype":"protein_coding","ncbi_id":"11013","summary":null,"start":102513676,"end":102516784,"strand":-1,"description":"thymosin beta 15a [Source:HGNC Symbol;Acc:HGNC:30744]"}, {"versioned_ensembl_gene_id":"ENSG00000234611.1","gene_symbol":"OR2AT2P","gene_name":"olfactory receptor family 2 subfamily AT member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:19619]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"390224","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":75071148,"end":75072052,"strand":-1,"description":"olfactory receptor family 2 subfamily AT member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:19619]"}, {"versioned_ensembl_gene_id":"ENSG00000184459.8","gene_symbol":"BPIFC","gene_name":"BPI fold containing family C [Source:HGNC Symbol;Acc:HGNC:16503]","synonyms":"dJ149A16.7,BPIL2","biotype":"protein_coding","ncbi_id":"254240","summary":null,"start":32413847,"end":32464484,"strand":-1,"description":"BPI fold containing family C [Source:HGNC Symbol;Acc:HGNC:16503]"}, {"versioned_ensembl_gene_id":"ENSG00000215371.3","gene_symbol":"DEFB108C","gene_name":"defensin beta 108C [Source:HGNC Symbol;Acc:HGNC:30847]","synonyms":"DEFB108P2","biotype":"unprocessed_pseudogene","ncbi_id":"503837","summary":null,"start":7373114,"end":7377500,"strand":1,"description":"defensin beta 108C [Source:HGNC Symbol;Acc:HGNC:30847]"}, {"versioned_ensembl_gene_id":"ENSG00000123472.12","gene_symbol":"ATPAF1","gene_name":"ATP synthase mitochondrial F1 complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:18803]","synonyms":"FLJ22351,Atp11p,ATP11","biotype":"protein_coding","ncbi_id":"64756","summary":"This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 beta subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]","start":46632737,"end":46673867,"strand":-1,"description":"ATP synthase mitochondrial F1 complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:18803]"}, {"versioned_ensembl_gene_id":"ENSG00000147041.11","gene_symbol":"SYTL5","gene_name":"synaptotagmin like 5 [Source:HGNC Symbol;Acc:HGNC:15589]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94122","summary":"The protein encoded by this gene belongs to the synaptotagmin-like (Slp) protein family, which contains a unique homology domain at the N-terminus, referred to as the Slp homology domain (SHD). The SHD functions as a binding site for Rab27A, which plays a role in protein transport. Expression of this gene is restricted to placenta and liver, suggesting that it might be involved in Rab27A-dependent membrane trafficking in specific tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":38006582,"end":38128819,"strand":1,"description":"synaptotagmin like 5 [Source:HGNC Symbol;Acc:HGNC:15589]"}, {"versioned_ensembl_gene_id":"ENSG00000213621.3","gene_symbol":"RPSAP54","gene_name":"ribosomal protein SA pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642641","summary":null,"start":20961310,"end":20962195,"strand":1,"description":"ribosomal protein SA pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36373]"}, {"versioned_ensembl_gene_id":"ENSG00000250349.3","gene_symbol":"AF241726.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37349330,"end":38687674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206481.11","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"Em:AB023051.5,NFBD1,KIAA0170","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30689327,"end":30707408,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000142789.19","gene_symbol":"CELA3A","gene_name":"chymotrypsin like elastase family member 3A [Source:HGNC Symbol;Acc:HGNC:15944]","synonyms":"ELA3A,ELA3","biotype":"protein_coding","ncbi_id":"10136","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Unlike other elastases, elastase 3A has little elastolytic activity. Like most of the human elastases, elastase 3A is secreted from the pancreas as a zymogen and, like other serine proteases such as trypsin, chymotrypsin and kallikrein, it has a digestive function in the intestine. Elastase 3A preferentially cleaves proteins after alanine residues. Elastase 3A may also function in the intestinal transport and metabolism of cholesterol. Both elastase 3A and elastase 3B have been referred to as protease E and as elastase 1. [provided by RefSeq, Jul 2008]","start":22001656,"end":22012539,"strand":1,"description":"chymotrypsin like elastase family member 3A [Source:HGNC Symbol;Acc:HGNC:15944]"}, {"versioned_ensembl_gene_id":"ENSG00000233780.3","gene_symbol":"HNRNPA1P30","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39548]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"440125","summary":null,"start":20938564,"end":20949599,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39548]"}, {"versioned_ensembl_gene_id":"ENSG00000237307.2","gene_symbol":"SRRM1P3","gene_name":"serine/arginine repetitive matrix 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130190","summary":null,"start":136976417,"end":136985705,"strand":-1,"description":"serine/arginine repetitive matrix 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38164]"}, {"versioned_ensembl_gene_id":"ENSG00000126353.3","gene_symbol":"CCR7","gene_name":"C-C motif chemokine receptor 7 [Source:HGNC Symbol;Acc:HGNC:1608]","synonyms":"EBI1,CMKBR7,CDw197,CD197,BLR2","biotype":"protein_coding","ncbi_id":"1236","summary":"The protein encoded by this gene is a member of the G protein-coupled receptor family. This receptor was identified as a gene induced by the Epstein-Barr virus (EBV), and is thought to be a mediator of EBV effects on B lymphocytes. This receptor is expressed in various lymphoid tissues and activates B and T lymphocytes. It has been shown to control the migration of memory T cells to inflamed tissues, as well as stimulate dendritic cell maturation. The chemokine (C-C motif) ligand 19 (CCL19/ECL) has been reported to be a specific ligand of this receptor. Signals mediated by this receptor regulate T cell homeostasis in lymph nodes, and may also function in the activation and polarization of T cells, and in chronic inflammation pathogenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":40553769,"end":40565472,"strand":-1,"description":"C-C motif chemokine receptor 7 [Source:HGNC Symbol;Acc:HGNC:1608]"}, {"versioned_ensembl_gene_id":"ENSG00000198898.13","gene_symbol":"CAPZA2","gene_name":"capping actin protein of muscle Z-line alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:1490]","synonyms":"CAPZ,CAPPA2","biotype":"protein_coding","ncbi_id":"830","summary":"The protein encoded by this gene is a member of the F-actin capping protein alpha subunit family. It is the alpha subunit of the barbed-end actin binding protein Cap Z. By capping the barbed end of actin filaments, Cap Z regulates the growth of the actin filaments at the barbed end. [provided by RefSeq, Jul 2008]","start":116811070,"end":116922049,"strand":1,"description":"capping actin protein of muscle Z-line alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:1490]"}, {"versioned_ensembl_gene_id":"ENSG00000276011.1","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"cl-43,CD158B1,nkat6,CD158k","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754397,"end":54768727,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000219274.1","gene_symbol":"RPS20P2","gene_name":"ribosomal protein S20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14195]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"64726","summary":null,"start":1329078,"end":1329777,"strand":1,"description":"ribosomal protein S20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14195]"}, {"versioned_ensembl_gene_id":"ENSG00000100528.11","gene_symbol":"CNIH1","gene_name":"cornichon family AMPA receptor auxiliary protein 1 [Source:HGNC Symbol;Acc:HGNC:19431]","synonyms":"TGAM77,CNIL,CNIH","biotype":"protein_coding","ncbi_id":"10175","summary":null,"start":54423560,"end":54441431,"strand":-1,"description":"cornichon family AMPA receptor auxiliary protein 1 [Source:HGNC Symbol;Acc:HGNC:19431]"}, {"versioned_ensembl_gene_id":"ENSG00000273599.1","gene_symbol":"AL731571.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124996064,"end":125001491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135900.3","gene_symbol":"MRPL44","gene_name":"mitochondrial ribosomal protein L44 [Source:HGNC Symbol;Acc:HGNC:16650]","synonyms":"FLJ13990,FLJ12701","biotype":"protein_coding","ncbi_id":"65080","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":223957404,"end":223967714,"strand":1,"description":"mitochondrial ribosomal protein L44 [Source:HGNC Symbol;Acc:HGNC:16650]"}, {"versioned_ensembl_gene_id":"ENSG00000261760.8","gene_symbol":"AC140479.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110231106,"end":110272050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255109.5","gene_symbol":"AC090458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42183292,"end":42253712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106404.13","gene_symbol":"CLDN15","gene_name":"claudin 15 [Source:HGNC Symbol;Acc:HGNC:2036]","synonyms":null,"biotype":"protein_coding","ncbi_id":"24146","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2010]","start":101232092,"end":101238820,"strand":-1,"description":"claudin 15 [Source:HGNC Symbol;Acc:HGNC:2036]"}, {"versioned_ensembl_gene_id":"ENSG00000271218.1","gene_symbol":"AL033384.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53918974,"end":53920788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276840.1","gene_symbol":"PMS2P10","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:9124]","synonyms":"PMSR4,PMS2L10","biotype":"unprocessed_pseudogene","ncbi_id":"100288713","summary":null,"start":75288120,"end":75299795,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:9124]"}, {"versioned_ensembl_gene_id":"ENSG00000227158.1","gene_symbol":"AC073621.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17422681,"end":17423704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234443.9","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"NG25,G6D,MEGT1,C6orf23,Ly6-D","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31697525,"end":31699973,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000103490.13","gene_symbol":"PYCARD","gene_name":"PYD and CARD domain containing [Source:HGNC Symbol;Acc:HGNC:16608]","synonyms":"TMS-1,CARD5,ASC","biotype":"protein_coding","ncbi_id":"29108","summary":"This gene encodes an adaptor protein that is composed of two protein-protein interaction domains: a N-terminal PYRIN-PAAD-DAPIN domain (PYD) and a C-terminal caspase-recruitment domain (CARD). The PYD and CARD domains are members of the six-helix bundle death domain-fold superfamily that mediates assembly of large signaling complexes in the inflammatory and apoptotic signaling pathways via the activation of caspase. In normal cells, this protein is localized to the cytoplasm; however, in cells undergoing apoptosis, it forms ball-like aggregates near the nuclear periphery. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31201485,"end":31203450,"strand":-1,"description":"PYD and CARD domain containing [Source:HGNC Symbol;Acc:HGNC:16608]"}, {"versioned_ensembl_gene_id":"ENSG00000215030.5","gene_symbol":"AC073621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17383377,"end":17384012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259507.1","gene_symbol":"AC103968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98466840,"end":98467412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215187.10","gene_symbol":"FAM166B","gene_name":"family with sequence similarity 166 member B [Source:HGNC Symbol;Acc:HGNC:34242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730112","summary":null,"start":35561831,"end":35563899,"strand":-1,"description":"family with sequence similarity 166 member B [Source:HGNC Symbol;Acc:HGNC:34242]"}, {"versioned_ensembl_gene_id":"ENSG00000164118.12","gene_symbol":"CEP44","gene_name":"centrosomal protein 44 [Source:HGNC Symbol;Acc:HGNC:29356]","synonyms":"KIAA1712","biotype":"protein_coding","ncbi_id":"80817","summary":null,"start":174283677,"end":174333380,"strand":1,"description":"centrosomal protein 44 [Source:HGNC Symbol;Acc:HGNC:29356]"}, {"versioned_ensembl_gene_id":"ENSG00000174891.12","gene_symbol":"RSRC1","gene_name":"arginine and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24152]","synonyms":"SRrp53,SFRS21,MGC12197,BM-011","biotype":"protein_coding","ncbi_id":"51319","summary":"This gene encodes a member of the serine and arginine rich-related protein family. The encoded protein is involved in both constitutive and alternative mRNA splicing. This gene may be associated with schizophrenia. A pseudogene of this gene is located on chromosome 9. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]","start":158105855,"end":158545730,"strand":1,"description":"arginine and serine rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:24152]"}, {"versioned_ensembl_gene_id":"ENSG00000235152.1","gene_symbol":"AL353052.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":232160091,"end":232185643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255388.5","gene_symbol":"AC021006.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41518895,"end":41714448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255853.1","gene_symbol":"AC006065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126510910,"end":126511711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131966.13","gene_symbol":"ACTR10","gene_name":"actin related protein 10 homolog [Source:HGNC Symbol;Acc:HGNC:17372]","synonyms":"Arp11,Arp10,ACTR11,HARP11","biotype":"protein_coding","ncbi_id":"55860","summary":null,"start":58200080,"end":58235636,"strand":1,"description":"actin related protein 10 homolog [Source:HGNC Symbol;Acc:HGNC:17372]"}, {"versioned_ensembl_gene_id":"ENSG00000275871.1","gene_symbol":"AC131025.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149425771,"end":149428289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227293.1","gene_symbol":"AC118345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66235377,"end":66236213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276564.1","gene_symbol":"AC130650.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14150833,"end":14153235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229249.6","gene_symbol":"LINC00446","gene_name":"long intergenic non-protein coding RNA 446 [Source:HGNC Symbol;Acc:HGNC:42783]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874175","summary":null,"start":78012883,"end":78053595,"strand":1,"description":"long intergenic non-protein coding RNA 446 [Source:HGNC Symbol;Acc:HGNC:42783]"}, {"versioned_ensembl_gene_id":"ENSG00000259969.1","gene_symbol":"AL049838.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":57993545,"end":57994525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237988.4","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"HS6M1-14,OR2I2,OR2I4P,OR2I1,OR2I3P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29550407,"end":29557721,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000204787.8","gene_symbol":"REG1CP","gene_name":"regenerating family member 1 gamma, pseudogene [Source:HGNC Symbol;Acc:HGNC:9953]","synonyms":"RS,REGL,REG1P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5969","summary":null,"start":79135503,"end":79138427,"strand":-1,"description":"regenerating family member 1 gamma, pseudogene [Source:HGNC Symbol;Acc:HGNC:9953]"}, {"versioned_ensembl_gene_id":"ENSG00000271558.1","gene_symbol":"AL391813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187506838,"end":187507119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105877.17","gene_symbol":"DNAH11","gene_name":"dynein axonemal heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:2942]","synonyms":"DPL11,DNHBL,Dnahc11,DNAHBL,CILD7","biotype":"protein_coding","ncbi_id":"8701","summary":"This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility. [provided by RefSeq, Mar 2013]","start":21543215,"end":21901839,"strand":1,"description":"dynein axonemal heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:2942]"}, {"versioned_ensembl_gene_id":"ENSG00000238013.1","gene_symbol":"AC109583.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46798123,"end":46798390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225400.1","gene_symbol":"RAB28P5","gene_name":"RAB28, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51547]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128416","summary":null,"start":136847384,"end":136848034,"strand":1,"description":"RAB28, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51547]"}, {"versioned_ensembl_gene_id":"ENSG00000269580.2","gene_symbol":"AC020914.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51508573,"end":51509311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087128.9","gene_symbol":"TMPRSS11E","gene_name":"transmembrane protease, serine 11E [Source:HGNC Symbol;Acc:HGNC:24465]","synonyms":"TMPRSS11E2,DESC1","biotype":"protein_coding","ncbi_id":"28983","summary":null,"start":68447449,"end":68497604,"strand":1,"description":"transmembrane protease, serine 11E [Source:HGNC Symbol;Acc:HGNC:24465]"}, {"versioned_ensembl_gene_id":"ENSG00000277972.1","gene_symbol":"CISD3","gene_name":"CDGSH iron sulfur domain 3 [Source:HGNC Symbol;Acc:HGNC:27578]","synonyms":"Miner2","biotype":"protein_coding","ncbi_id":"284106","summary":"CISD3 is a member of the CDGSH domain-containing family, which may play a role in regulating electron transport and oxidative phosphorylation (Wiley et al., 2007 [PubMed 17376863]).[supplied by OMIM, Apr 2008]","start":38730235,"end":38735044,"strand":1,"description":"CDGSH iron sulfur domain 3 [Source:HGNC Symbol;Acc:HGNC:27578]"}, {"versioned_ensembl_gene_id":"ENSG00000160271.14","gene_symbol":"RALGDS","gene_name":"ral guanine nucleotide dissociation stimulator [Source:HGNC Symbol;Acc:HGNC:9842]","synonyms":"RGF,RGDS,RalGEF","biotype":"protein_coding","ncbi_id":"5900","summary":"Guanine nucleotide dissociation stimulators (GDSs, or exchange factors), such as RALGDS, are effectors of Ras-related GTPases (see MIM 190020) that participate in signaling for a variety of cellular processes.[supplied by OMIM, Nov 2010]","start":133097720,"end":133149334,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator [Source:HGNC Symbol;Acc:HGNC:9842]"}, {"versioned_ensembl_gene_id":"ENSG00000168418.7","gene_symbol":"KCNG4","gene_name":"potassium voltage-gated channel modifier subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:19697]","synonyms":"Kv6.4","biotype":"protein_coding","ncbi_id":"93107","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This member functions as a modulatory subunit. The gene has strong expression in brain. Multiple alternatively spliced variants have been found in normal and cancerous tissues. [provided by RefSeq, Jul 2008]","start":84218667,"end":84239750,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:19697]"}, {"versioned_ensembl_gene_id":"ENSG00000266397.1","gene_symbol":"AP000919.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2967018,"end":2985410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204398.5","gene_symbol":"AL359649.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111588201,"end":111672608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260545.1","gene_symbol":"AC026771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58116885,"end":58119353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267852.1","gene_symbol":"AC119396.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7390522,"end":7395039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228592.1","gene_symbol":"D21S2088E","gene_name":"D21S2088E [Source:NCBI gene;Acc:266917]","synonyms":null,"biotype":"lincRNA","ncbi_id":"266917","summary":null,"start":23361104,"end":23384861,"strand":-1,"description":"D21S2088E [Source:NCBI gene;Acc:266917]"}, {"versioned_ensembl_gene_id":"ENSG00000283443.1","gene_symbol":"AC018688.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30545601,"end":30551470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233664.1","gene_symbol":"NDUFS5P3","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44041]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288149","summary":null,"start":52709122,"end":52709442,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44041]"}, {"versioned_ensembl_gene_id":"ENSG00000179284.5","gene_symbol":"DAND5","gene_name":"DAN domain BMP antagonist family member 5 [Source:HGNC Symbol;Acc:HGNC:26780]","synonyms":"GREM3,FLJ38607,DTE,DANTE,Coco,CKTSF1B3,CER2","biotype":"protein_coding","ncbi_id":"199699","summary":"This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to bind Nodal and to inhibit the Nodal signaling pathway which patterns left/right body asymmetry. [provided by RefSeq, Jul 2008]","start":12965159,"end":12974762,"strand":1,"description":"DAN domain BMP antagonist family member 5 [Source:HGNC Symbol;Acc:HGNC:26780]"}, {"versioned_ensembl_gene_id":"ENSG00000263862.1","gene_symbol":"LINC01543","gene_name":"long intergenic non-protein coding RNA 1543 [Source:HGNC Symbol;Acc:HGNC:51310]","synonyms":"TCONS_00026302","biotype":"lincRNA","ncbi_id":"100506787","summary":null,"start":26422995,"end":26426101,"strand":1,"description":"long intergenic non-protein coding RNA 1543 [Source:HGNC Symbol;Acc:HGNC:51310]"}, {"versioned_ensembl_gene_id":"ENSG00000249379.1","gene_symbol":"AL033397.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53503185,"end":53506919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162267.12","gene_symbol":"ITIH3","gene_name":"inter-alpha-trypsin inhibitor heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:6168]","synonyms":"H3P","biotype":"protein_coding","ncbi_id":"3699","summary":"This gene encodes the heavy chain subunit of the pre-alpha-trypsin inhibitor complex. This complex may stabilize the extracellular matrix through its ability to bind hyaluronic acid. Polymorphisms of this gene may be associated with increased risk for schizophrenia and major depressive disorder. This gene is present in an inter-alpha-trypsin inhibitor family gene cluster on chromosome 3. [provided by RefSeq, Jul 2015]","start":52794768,"end":52809009,"strand":1,"description":"inter-alpha-trypsin inhibitor heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:6168]"}, {"versioned_ensembl_gene_id":"ENSG00000249459.8","gene_symbol":"ZNF286B","gene_name":"zinc finger protein 286B [Source:HGNC Symbol;Acc:HGNC:33241]","synonyms":"ZNF590,ZNF286L,ZNF286C","biotype":"protein_coding","ncbi_id":"729288","summary":null,"start":18658429,"end":18682262,"strand":-1,"description":"zinc finger protein 286B [Source:HGNC Symbol;Acc:HGNC:33241]"}, {"versioned_ensembl_gene_id":"ENSG00000279234.1","gene_symbol":"AC142525.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69605896,"end":69607737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239365.2","gene_symbol":"AL590326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104830838,"end":104831171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255595.2","gene_symbol":"AC005885.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":126191263,"end":126361065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254998.1","gene_symbol":"AP003181.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105157927,"end":105531697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254767.1","gene_symbol":"OR2AL1P","gene_name":"olfactory receptor family 2 subfamily AL member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14712]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79547","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":105194440,"end":105194946,"strand":-1,"description":"olfactory receptor family 2 subfamily AL member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14712]"}, {"versioned_ensembl_gene_id":"ENSG00000284486.1","gene_symbol":"AL513315.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":206767602,"end":206770575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230622.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31611083,"end":31611356,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000224487.8","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29373120,"end":29449634,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000054277.13","gene_symbol":"OPN3","gene_name":"opsin 3 [Source:HGNC Symbol;Acc:HGNC:14007]","synonyms":"encephalopsin,ECPN,PPP1R116,NMO-1,ERO","biotype":"protein_coding","ncbi_id":"23596","summary":"Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. In addition to the visual opsins, mammals possess several photoreceptive non-visual opsins that are expressed in extraocular tissues. This gene, opsin 3, is strongly expressed in brain and testis and weakly expressed in liver, placenta, heart, lung, skeletal muscle, kidney, and pancreas. The gene may also be expressed in the retina. The protein has the canonical features of a photoreceptive opsin protein. [provided by RefSeq, Jul 2008]","start":241590102,"end":241677376,"strand":-1,"description":"opsin 3 [Source:HGNC Symbol;Acc:HGNC:14007]"}, {"versioned_ensembl_gene_id":"ENSG00000249256.2","gene_symbol":"ATP5LP3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:13216]","synonyms":"ATP5KP3","biotype":"processed_pseudogene","ncbi_id":"53409","summary":null,"start":24658072,"end":24658375,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:13216]"}, {"versioned_ensembl_gene_id":"ENSG00000135457.9","gene_symbol":"TFCP2","gene_name":"transcription factor CP2 [Source:HGNC Symbol;Acc:HGNC:11748]","synonyms":"TFCP2C,LSF,LBP-1C,CP2","biotype":"protein_coding","ncbi_id":"7024","summary":"This gene encodes a transcription factor that binds the alpha-globin promoter and activates transcription of the alpha-globin gene. The encoded protein regulates erythroid gene expression, plays a role in the transcriptional switch of globin gene promoters, and it activates many other cellular and viral gene promoters. The gene product interacts with certain inflammatory response factors, and polymorphisms of this gene may be involved in the pathogenesis of Alzheimer's disease. [provided by RefSeq, Mar 2010]","start":51093663,"end":51173134,"strand":-1,"description":"transcription factor CP2 [Source:HGNC Symbol;Acc:HGNC:11748]"}, {"versioned_ensembl_gene_id":"ENSG00000230328.2","gene_symbol":"AL359893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101358932,"end":101361242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236763.2","gene_symbol":"TRMT112P4","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288173","summary":null,"start":101356466,"end":101356844,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44023]"}, {"versioned_ensembl_gene_id":"ENSG00000254006.5","gene_symbol":"AC104232.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64801236,"end":64817573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183921.7","gene_symbol":"SDR42E2","gene_name":"short chain dehydrogenase/reductase family 42E, member 2 [Source:HGNC Symbol;Acc:HGNC:35414]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288072","summary":null,"start":22165583,"end":22191754,"strand":1,"description":"short chain dehydrogenase/reductase family 42E, member 2 [Source:HGNC Symbol;Acc:HGNC:35414]"}, {"versioned_ensembl_gene_id":"ENSG00000230066.5","gene_symbol":"FAM197Y3","gene_name":"family with sequence similarity 197 Y-linked member 3 [Source:HGNC Symbol;Acc:HGNC:37465]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107987341","summary":null,"start":9497287,"end":9506566,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 3 [Source:HGNC Symbol;Acc:HGNC:37465]"}, {"versioned_ensembl_gene_id":"ENSG00000165164.13","gene_symbol":"CFAP47","gene_name":"cilia and flagella associated protein 47 [Source:HGNC Symbol;Acc:HGNC:26708]","synonyms":"RP13-11B7.1,MGC34831,FLJ36601,CXorf59,CXorf30,CXorf22,CHDC2","biotype":"protein_coding","ncbi_id":"286464","summary":"While this gene is well-supported by transcript data, no functional information on its protein product is currently available. [provided by RefSeq, Dec 2009]","start":35919734,"end":36385319,"strand":1,"description":"cilia and flagella associated protein 47 [Source:HGNC Symbol;Acc:HGNC:26708]"}, {"versioned_ensembl_gene_id":"ENSG00000134686.18","gene_symbol":"PHC2","gene_name":"polyhomeotic homolog 2 [Source:HGNC Symbol;Acc:HGNC:3183]","synonyms":"HPH2,EDR2","biotype":"protein_coding","ncbi_id":"1912","summary":"In Drosophila melanogaster, the 'Polycomb' group (PcG) of genes are part of a cellular memory system that is responsible for the stable inheritance of gene activity. PcG proteins form a large multimeric, chromatin-associated protein complex. The protein encoded by this gene has homology to the Drosophila PcG protein 'polyhomeotic' (Ph) and is known to heterodimerize with EDR1 and colocalize with BMI1 in interphase nuclei of human cells. The specific function in human cells has not yet been determined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":33323623,"end":33431052,"strand":-1,"description":"polyhomeotic homolog 2 [Source:HGNC Symbol;Acc:HGNC:3183]"}, {"versioned_ensembl_gene_id":"ENSG00000082684.14","gene_symbol":"SEMA5B","gene_name":"semaphorin 5B [Source:HGNC Symbol;Acc:HGNC:10737]","synonyms":"SemG,SEMAG,KIAA1445,FLJ10372","biotype":"protein_coding","ncbi_id":"54437","summary":"This gene encodes a member of the semaphorin protein family which regulates axon growth during development of the nervous system. The encoded protein has a characteristic Sema domain near the N-terminus, through which semaphorins bind to plexin, and five thrombospondin type 1 repeats in the C-terminal region of the protein. The protein product may be cleaved and exist as a secreted molecule (PMID: 19463192). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":122909193,"end":123028605,"strand":-1,"description":"semaphorin 5B [Source:HGNC Symbol;Acc:HGNC:10737]"}, {"versioned_ensembl_gene_id":"ENSG00000260755.1","gene_symbol":"AC010542.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66509437,"end":66510048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166546.13","gene_symbol":"BEAN1","gene_name":"brain expressed associated with NEDD4 1 [Source:HGNC Symbol;Acc:HGNC:24160]","synonyms":"SCA31","biotype":"protein_coding","ncbi_id":"146227","summary":"The protein encoded by this gene is one of several proteins that interact with NEDD4, a member of a family of ubiquitin-protein ligases. These proteins have PY motifs in common that bind to the WW domains of NEDD4. NEDD4 is developmentally regulated, and is highly expressed in embryonic tissues. Mutations in this gene (i.e., intronic insertions of >100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":66427297,"end":66493529,"strand":1,"description":"brain expressed associated with NEDD4 1 [Source:HGNC Symbol;Acc:HGNC:24160]"}, {"versioned_ensembl_gene_id":"ENSG00000235640.1","gene_symbol":"AC092646.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123695302,"end":123697396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214770.2","gene_symbol":"AL161756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64329431,"end":64338599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259191.2","gene_symbol":"AC027237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69434466,"end":69435120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245164.6","gene_symbol":"LINC00861","gene_name":"long intergenic non-protein coding RNA 861 [Source:HGNC Symbol;Acc:HGNC:45133]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100130231","summary":null,"start":125922308,"end":125951249,"strand":-1,"description":"long intergenic non-protein coding RNA 861 [Source:HGNC Symbol;Acc:HGNC:45133]"}, {"versioned_ensembl_gene_id":"ENSG00000205138.3","gene_symbol":"SDHAF1","gene_name":"succinate dehydrogenase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:33867]","synonyms":"LYRM8","biotype":"protein_coding","ncbi_id":"644096","summary":"The succinate dehydrogenase (SDH) complex (or complex II) of the mitochondrial respiratory chain is composed of 4 individual subunits. The protein encoded by this gene resides in the mitochondria, and is essential for SDH assembly, but does not physically associate with the complex in vivo. Mutations in this gene are associated with SDH-defective infantile leukoencephalopathy (mitochondrial complex II deficiency).[provided by RefSeq, Mar 2010]","start":35995199,"end":35996315,"strand":1,"description":"succinate dehydrogenase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:33867]"}, {"versioned_ensembl_gene_id":"ENSG00000230165.1","gene_symbol":"AURKAPS2","gene_name":"aurora kinase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18612]","synonyms":"STK6LP","biotype":"processed_pseudogene","ncbi_id":"386665","summary":null,"start":114246074,"end":114246714,"strand":1,"description":"aurora kinase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18612]"}, {"versioned_ensembl_gene_id":"ENSG00000251313.1","gene_symbol":"AC073648.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9030286,"end":9031066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271057.1","gene_symbol":"AC073648.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9020857,"end":9021161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278090.1","gene_symbol":"AC036108.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99028538,"end":99031053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010030.13","gene_symbol":"ETV7","gene_name":"ETS variant 7 [Source:HGNC Symbol;Acc:HGNC:18160]","synonyms":"TEL2,TEL-2","biotype":"protein_coding","ncbi_id":"51513","summary":"The protein encoded by this gene belongs to the ETS family of transcription factors, which is a large group of evolutionarily conserved transcriptional regulators that play an important role in a variety of cellular processes throughout development and differentiation, and are involved in oncogenesis as well. This protein is predominantly expressed in hematopoietic tissues. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene (PMID:11108721).[provided by RefSeq, May 2011]","start":36354091,"end":36387800,"strand":-1,"description":"ETS variant 7 [Source:HGNC Symbol;Acc:HGNC:18160]"}, {"versioned_ensembl_gene_id":"ENSG00000229977.2","gene_symbol":"AC073264.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143532749,"end":143533164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236918.1","gene_symbol":"BX908738.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29262684,"end":29264060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279603.1","gene_symbol":"AP000720.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89300709,"end":89301477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077498.8","gene_symbol":"TYR","gene_name":"tyrosinase [Source:HGNC Symbol;Acc:HGNC:12442]","synonyms":"OCA1A,OCA1,OCAIA","biotype":"protein_coding","ncbi_id":"7299","summary":"The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene. [provided by RefSeq, Oct 2008]","start":89177452,"end":89295759,"strand":1,"description":"tyrosinase [Source:HGNC Symbol;Acc:HGNC:12442]"}, {"versioned_ensembl_gene_id":"ENSG00000215612.7","gene_symbol":"HMX1","gene_name":"H6 family homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5017]","synonyms":"NKX5-3,H6","biotype":"protein_coding","ncbi_id":"3166","summary":"This gene encodes a transcription factor that belongs to the H6 family of homeobox proteins. This protein can bind a 5'-CAAG-3' core DNA sequence, and it is involved in the development of craniofacial structures. Mutations in this gene cause oculoauricular syndrome, a disorder of the eye and external ear. [provided by RefSeq, Oct 2009]","start":8846076,"end":8871817,"strand":-1,"description":"H6 family homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5017]"}, {"versioned_ensembl_gene_id":"ENSG00000226771.1","gene_symbol":"AP001136.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21223295,"end":21226829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182183.14","gene_symbol":"FAM159A","gene_name":"family with sequence similarity 159 member A [Source:HGNC Symbol;Acc:HGNC:28757]","synonyms":"MGC52498","biotype":"protein_coding","ncbi_id":"348378","summary":null,"start":52633344,"end":52669683,"strand":1,"description":"family with sequence similarity 159 member A [Source:HGNC Symbol;Acc:HGNC:28757]"}, {"versioned_ensembl_gene_id":"ENSG00000219653.1","gene_symbol":"GCNT1P4","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462829","summary":null,"start":63857441,"end":63857769,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37974]"}, {"versioned_ensembl_gene_id":"ENSG00000205267.5","gene_symbol":"DGAT2L7P","gene_name":"diacylglycerol O-acyltransferase 2 like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44367]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646409","summary":null,"start":101201809,"end":101203526,"strand":-1,"description":"diacylglycerol O-acyltransferase 2 like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44367]"}, {"versioned_ensembl_gene_id":"ENSG00000267727.1","gene_symbol":"AC008738.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33301279,"end":33301940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254903.1","gene_symbol":"OR8L1P","gene_name":"olfactory receptor family 8 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15316]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81164","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56381635,"end":56382589,"strand":1,"description":"olfactory receptor family 8 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15316]"}, {"versioned_ensembl_gene_id":"ENSG00000275212.1","gene_symbol":"AC005858.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126032995,"end":126043485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256276.1","gene_symbol":"AC005186.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125983702,"end":125986234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262732.1","gene_symbol":"AC010401.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13930677,"end":13935635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229245.2","gene_symbol":"AL359636.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122403407,"end":122448977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242391.2","gene_symbol":"AC099677.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52881216,"end":52881730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230728.1","gene_symbol":"AL590093.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":54621477,"end":54628438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275837.3","gene_symbol":"SMARCB1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 [Source:HGNC Symbol;Acc:HGNC:11103]","synonyms":"RDT,PPP1R144,Ini1,Snr1,hSNFS,SNF5L1,BAF47,Sfh1p","biotype":"protein_coding","ncbi_id":"6598","summary":"The protein encoded by this gene is part of a complex that relieves repressive chromatin structures, allowing the transcriptional machinery to access its targets more effectively. The encoded nuclear protein may also bind to and enhance the DNA joining activity of HIV-1 integrase. This gene has been found to be a tumor suppressor, and mutations in it have been associated with malignant rhabdoid tumors. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":23786963,"end":23834516,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 [Source:HGNC Symbol;Acc:HGNC:11103]"}, {"versioned_ensembl_gene_id":"ENSG00000260120.1","gene_symbol":"AC104066.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52680609,"end":52692649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139428.11","gene_symbol":"MMAB","gene_name":"methylmalonic aciduria (cobalamin deficiency) cblB type [Source:HGNC Symbol;Acc:HGNC:19331]","synonyms":"CFAP23,cblB","biotype":"protein_coding","ncbi_id":"326625","summary":"This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]","start":109553737,"end":109573874,"strand":-1,"description":"methylmalonic aciduria (cobalamin deficiency) cblB type [Source:HGNC Symbol;Acc:HGNC:19331]"}, {"versioned_ensembl_gene_id":"ENSG00000228286.3","gene_symbol":"AP000593.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72249856,"end":72251288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249201.2","gene_symbol":"CTD-3080P12.3","gene_name":"uncharacterized LOC101928857 [Source:NCBI gene;Acc:101928857]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928857","summary":null,"start":1173141,"end":1178605,"strand":-1,"description":"uncharacterized LOC101928857 [Source:NCBI gene;Acc:101928857]"}, {"versioned_ensembl_gene_id":"ENSG00000132688.10","gene_symbol":"NES","gene_name":"nestin [Source:HGNC Symbol;Acc:HGNC:7756]","synonyms":"FLJ21841","biotype":"protein_coding","ncbi_id":"10763","summary":"This gene encodes a member of the intermediate filament protein family and is expressed primarily in nerve cells. [provided by RefSeq, Sep 2011]","start":156668763,"end":156677397,"strand":-1,"description":"nestin [Source:HGNC Symbol;Acc:HGNC:7756]"}, {"versioned_ensembl_gene_id":"ENSG00000251608.2","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"polymorphic_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29414928,"end":29418905,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000283283.1","gene_symbol":"AC013268.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":110022447,"end":110035270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206474.8","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439306,"end":29440977,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000220154.2","gene_symbol":"AL355796.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79278105,"end":79278427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277858.1","gene_symbol":"H2AFB2","gene_name":"H2A histone family member B2 [Source:HGNC Symbol;Acc:HGNC:18298]","synonyms":null,"biotype":"protein_coding","ncbi_id":"474381","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the middle copy. [provided by RefSeq, Oct 2015]","start":155380787,"end":155381134,"strand":1,"description":"H2A histone family member B2 [Source:HGNC Symbol;Acc:HGNC:18298]"}, {"versioned_ensembl_gene_id":"ENSG00000197181.11","gene_symbol":"PIWIL2","gene_name":"piwi like RNA-mediated gene silencing 2 [Source:HGNC Symbol;Acc:HGNC:17644]","synonyms":"Mili,HILI,FLJ10351,CT80","biotype":"protein_coding","ncbi_id":"55124","summary":"PIWIL2 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003 [PubMed 12906857]).[supplied by OMIM, Mar 2008]","start":22275297,"end":22357563,"strand":1,"description":"piwi like RNA-mediated gene silencing 2 [Source:HGNC Symbol;Acc:HGNC:17644]"}, {"versioned_ensembl_gene_id":"ENSG00000232141.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30021567,"end":30022857,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000227027.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29888080,"end":29889211,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000166439.5","gene_symbol":"RNF169","gene_name":"ring finger protein 169 [Source:HGNC Symbol;Acc:HGNC:26961]","synonyms":"KIAA1991","biotype":"protein_coding","ncbi_id":"254225","summary":null,"start":74748868,"end":74842413,"strand":1,"description":"ring finger protein 169 [Source:HGNC Symbol;Acc:HGNC:26961]"}, {"versioned_ensembl_gene_id":"ENSG00000237870.6","gene_symbol":"AC073130.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":116275606,"end":116286734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071553.16","gene_symbol":"ATP6AP1","gene_name":"ATPase H+ transporting accessory protein 1 [Source:HGNC Symbol;Acc:HGNC:868]","synonyms":"XAP3,XAP-3,VATPS1,ORF,CF2,ATP6S1,ATP6IP1,Ac45,16A","biotype":"protein_coding","ncbi_id":"537","summary":"This gene encodes a component of a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. Vacuolar ATPase (V-ATPase) is comprised of a cytosolic V1 (site of the ATP catalytic site) and a transmembrane V0 domain. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor-mediated endocytosis. The encoded protein of this gene may assist in the V-ATPase-mediated acidification of neuroendocrine secretory granules. This protein may also play a role in early development. [provided by RefSeq, Aug 2013]","start":154428632,"end":154436516,"strand":1,"description":"ATPase H+ transporting accessory protein 1 [Source:HGNC Symbol;Acc:HGNC:868]"}, {"versioned_ensembl_gene_id":"ENSG00000157181.15","gene_symbol":"C1orf27","gene_name":"chromosome 1 open reading frame 27 [Source:HGNC Symbol;Acc:HGNC:24299]","synonyms":"TTG1,odr-4,FLJ20505","biotype":"protein_coding","ncbi_id":"54953","summary":null,"start":186375838,"end":186421378,"strand":1,"description":"chromosome 1 open reading frame 27 [Source:HGNC Symbol;Acc:HGNC:24299]"}, {"versioned_ensembl_gene_id":"ENSG00000279520.1","gene_symbol":"AC093525.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2516658,"end":2517999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234811.1","gene_symbol":"AL161932.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32111644,"end":32111789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230106.1","gene_symbol":"SNRPCP15","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49830]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310857","summary":null,"start":7170550,"end":7170741,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49830]"}, {"versioned_ensembl_gene_id":"ENSG00000099960.12","gene_symbol":"SLC7A4","gene_name":"solute carrier family 7 member 4 [Source:HGNC Symbol;Acc:HGNC:11062]","synonyms":"VH,HCAT3,CAT-4","biotype":"protein_coding","ncbi_id":"6545","summary":null,"start":21028718,"end":21032840,"strand":-1,"description":"solute carrier family 7 member 4 [Source:HGNC Symbol;Acc:HGNC:11062]"}, {"versioned_ensembl_gene_id":"ENSG00000259041.1","gene_symbol":"AC015722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98282075,"end":98285907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082482.13","gene_symbol":"KCNK2","gene_name":"potassium two pore domain channel subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:6277]","synonyms":"TREK-1,K2p2.1","biotype":"protein_coding","ncbi_id":"3776","summary":"This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":215005775,"end":215237093,"strand":1,"description":"potassium two pore domain channel subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:6277]"}, {"versioned_ensembl_gene_id":"ENSG00000280231.1","gene_symbol":"AL031719.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1553655,"end":1554130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282921.1","gene_symbol":"CFTRP2","gene_name":"cystic fibrosis transmembrane conductance regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107080633","summary":null,"start":29641778,"end":29641976,"strand":1,"description":"cystic fibrosis transmembrane conductance regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51351]"}, {"versioned_ensembl_gene_id":"ENSG00000251292.1","gene_symbol":"ERVH-1","gene_name":"endogenous retrovirus group H member 1 [Source:HGNC Symbol;Acc:HGNC:39053]","synonyms":"HERV-H4p15.2","biotype":"lincRNA","ncbi_id":"100616446","summary":null,"start":23723262,"end":23733579,"strand":-1,"description":"endogenous retrovirus group H member 1 [Source:HGNC Symbol;Acc:HGNC:39053]"}, {"versioned_ensembl_gene_id":"ENSG00000237285.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32325219,"end":32326178,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000277427.1","gene_symbol":"AL671511.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32255284,"end":32350039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228364.1","gene_symbol":"AL662791.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076573,"end":29077168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000015568.12","gene_symbol":"RGPD5","gene_name":"RANBP2-like and GRIP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:32418]","synonyms":"RGP5,DKFZp686I1842,BS-63","biotype":"protein_coding","ncbi_id":"84220","summary":"RAN is a small GTP-binding protein of the RAS superfamily that is associated with the nuclear membrane and is thought to control a variety of cellular functions through its interactions with other proteins. This gene shares a high degree of sequence identity with RANBP2, a large RAN-binding protein localized at the cytoplasmic side of the nuclear pore complex. It is believed that this RANBP2 gene family member arose from a duplication event 3 Mb distal to RANBP2. Alternative splicing has been observed for this locus and two variants are described. Additional splicing is suggested but complete sequence for further transcripts has not been determined. [provided by RefSeq, Jul 2008]","start":109792758,"end":109857695,"strand":1,"description":"RANBP2-like and GRIP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:32418]"}, {"versioned_ensembl_gene_id":"ENSG00000267011.5","gene_symbol":"AC011498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4457962,"end":4471493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270677.1","gene_symbol":"AC007363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36656322,"end":36656941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212766.9","gene_symbol":"EWSAT1","gene_name":"Ewing sarcoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:26596]","synonyms":"TMEM84,NCRNA00277,LINC00277,FLJ33768","biotype":"lincRNA","ncbi_id":"283673","summary":null,"start":69072926,"end":69095820,"strand":1,"description":"Ewing sarcoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:26596]"}, {"versioned_ensembl_gene_id":"ENSG00000234379.1","gene_symbol":"HMGB1P48","gene_name":"high mobility group box 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:39281]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128639","summary":null,"start":45530927,"end":45532139,"strand":1,"description":"high mobility group box 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:39281]"}, {"versioned_ensembl_gene_id":"ENSG00000277545.1","gene_symbol":"AL356752.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":112811566,"end":112812158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141956.13","gene_symbol":"PRDM15","gene_name":"PR/SET domain 15 [Source:HGNC Symbol;Acc:HGNC:13999]","synonyms":"C21orf83,ZNF298","biotype":"protein_coding","ncbi_id":"63977","summary":null,"start":41798225,"end":41879482,"strand":-1,"description":"PR/SET domain 15 [Source:HGNC Symbol;Acc:HGNC:13999]"}, {"versioned_ensembl_gene_id":"ENSG00000240959.1","gene_symbol":"ST13P14","gene_name":"ST13, Hsp70 interacting protein pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422602","summary":null,"start":50876712,"end":50877657,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38849]"}, {"versioned_ensembl_gene_id":"ENSG00000258206.1","gene_symbol":"AC137768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85781892,"end":85782444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258815.1","gene_symbol":"AC131532.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85318060,"end":85342912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089169.14","gene_symbol":"RPH3A","gene_name":"rabphilin 3A [Source:HGNC Symbol;Acc:HGNC:17056]","synonyms":"rabphilin,KIAA0985,exophilin-1","biotype":"protein_coding","ncbi_id":"22895","summary":"The protein encoded by this gene is thought to be an effector for RAB3A, which is a small G protein that acts in the late stages of neurotransmitter exocytosis. The encoded protein may be involved in neurotransmitter release and synaptic vesicle traffic. [provided by RefSeq, Dec 2016]","start":112570380,"end":112898881,"strand":1,"description":"rabphilin 3A [Source:HGNC Symbol;Acc:HGNC:17056]"}, {"versioned_ensembl_gene_id":"ENSG00000258829.1","gene_symbol":"AC026888.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79072132,"end":79074767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236972.2","gene_symbol":"FABP5P1","gene_name":"fatty acid binding protein 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31059]","synonyms":"FABP5L1,FABP5","biotype":"processed_pseudogene","ncbi_id":"387934","summary":null,"start":73100575,"end":73100985,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31059]"}, {"versioned_ensembl_gene_id":"ENSG00000125787.11","gene_symbol":"GNRH2","gene_name":"gonadotropin releasing hormone 2 [Source:HGNC Symbol;Acc:HGNC:4420]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2797","summary":"This gene is a member of the gonadotropin-releasing hormone (GnRH) gene family. Proteins encoded by members of this gene family are proteolytically cleaved to form neuropeptides which, in part, regulate reproductive functions by stimulating the production and release of the gonadotropins follicle-stimulating hormone (FSH) and luteinizing hormone (LH). The human GNRH2 gene is predicted to encode a preproprotein from which a mature neuropeptide of 10 amino acids is cleaved. However, while the human genome retains the sequence for a functional GNRH2 decapeptide, translation of the human GNRH2 gene has not yet been demonstrated and the GNRH2 gene of chimpanzees, gorilla, and Sumatran orangutan have a premature stop at codon eight of the decapeptide sequence which suggests GNRH2 was a pseudogene in the hominid lineage. The GNRH2 gene is also believed to be a pseudogene in many other mammalian species such as mouse and cow. The receptor for this gene (GNRHR2) is predicted to be a pseudogene in human as well as many other mammalian species. The closely related GNRH1 and GNRHR1 genes are functional in human and other mammals and are generally functional in vertebrates. [provided by RefSeq, Mar 2019]","start":3043622,"end":3045747,"strand":1,"description":"gonadotropin releasing hormone 2 [Source:HGNC Symbol;Acc:HGNC:4420]"}, {"versioned_ensembl_gene_id":"ENSG00000158445.9","gene_symbol":"KCNB1","gene_name":"potassium voltage-gated channel subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:6231]","synonyms":"Kv2.1","biotype":"protein_coding","ncbi_id":"3745","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel and its activity is modulated by some other family members. [provided by RefSeq, Jul 2008]","start":49293394,"end":49484297,"strand":-1,"description":"potassium voltage-gated channel subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:6231]"}, {"versioned_ensembl_gene_id":"ENSG00000122641.10","gene_symbol":"INHBA","gene_name":"inhibin beta A subunit [Source:HGNC Symbol;Acc:HGNC:6066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3624","summary":"This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate a subunit of the dimeric activin and inhibin protein complexes. These complexes activate and inhibit, respectively, follicle stimulating hormone secretion from the pituitary gland. The encoded protein also plays a role in eye, tooth and testis development. Elevated expression of this gene may be associated with cancer cachexia in human patients. [provided by RefSeq, Aug 2016]","start":41667168,"end":41705834,"strand":-1,"description":"inhibin beta A subunit [Source:HGNC Symbol;Acc:HGNC:6066]"}, {"versioned_ensembl_gene_id":"ENSG00000185453.12","gene_symbol":"C19orf68","gene_name":"chromosome 19 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:34495]","synonyms":"LOC374920","biotype":"protein_coding","ncbi_id":"374920","summary":null,"start":48170692,"end":48197620,"strand":1,"description":"chromosome 19 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:34495]"}, {"versioned_ensembl_gene_id":"ENSG00000255204.1","gene_symbol":"AC036111.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55863932,"end":55881243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263547.1","gene_symbol":"AC011095.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":76122998,"end":76145255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188312.13","gene_symbol":"CENPP","gene_name":"centromere protein P [Source:HGNC Symbol;Acc:HGNC:32933]","synonyms":"RP11-19J3.3,CENP-P","biotype":"protein_coding","ncbi_id":"401541","summary":"CENPP is a subunit of a CENPH (MIM 605607)-CENPI (MIM 300065)-associated centromeric complex that targets CENPA (MIM 117139) to centromeres and is required for proper kinetochore function and mitotic progression (Okada et al., 2006 [PubMed 16622420]).[supplied by OMIM, Mar 2008]","start":92325484,"end":92620533,"strand":1,"description":"centromere protein P [Source:HGNC Symbol;Acc:HGNC:32933]"}, {"versioned_ensembl_gene_id":"ENSG00000227073.1","gene_symbol":"SDHDP2","gene_name":"succinate dehydrogenase complex subunit D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10685]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647081","summary":null,"start":135444461,"end":135444925,"strand":1,"description":"succinate dehydrogenase complex subunit D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10685]"}, {"versioned_ensembl_gene_id":"ENSG00000224781.1","gene_symbol":"EIF4A2P4","gene_name":"eukaryotic translation initiation factor 4A2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45101]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286512","summary":null,"start":52832704,"end":52833899,"strand":-1,"description":"eukaryotic translation initiation factor 4A2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45101]"}, {"versioned_ensembl_gene_id":"ENSG00000280870.2","gene_symbol":"MIR325HG","gene_name":"MIR325 host gene [Source:NCBI gene;Acc:101928469]","synonyms":"MIR384HG","biotype":"lincRNA","ncbi_id":"101928469","summary":null,"start":76657798,"end":77014532,"strand":-1,"description":"MIR325 host gene [Source:NCBI gene;Acc:101928469]"}, {"versioned_ensembl_gene_id":"ENSG00000147996.16","gene_symbol":"CBWD5","gene_name":"COBW domain containing 5 [Source:HGNC Symbol;Acc:HGNC:24584]","synonyms":null,"biotype":"protein_coding","ncbi_id":"220869","summary":null,"start":65668805,"end":65734041,"strand":1,"description":"COBW domain containing 5 [Source:HGNC Symbol;Acc:HGNC:24584]"}, {"versioned_ensembl_gene_id":"ENSG00000124541.6","gene_symbol":"RRP36","gene_name":"ribosomal RNA processing 36 [Source:HGNC Symbol;Acc:HGNC:21374]","synonyms":"dJ20C7.4,C6orf153","biotype":"protein_coding","ncbi_id":"88745","summary":"RRP36 functions at an early stage in the processing of 35S preribosomal RNA into the mature 18S species (Gerus et al., 2010 [PubMed 20038530]).[supplied by OMIM, Jul 2010]","start":43021645,"end":43034156,"strand":1,"description":"ribosomal RNA processing 36 [Source:HGNC Symbol;Acc:HGNC:21374]"}, {"versioned_ensembl_gene_id":"ENSG00000251637.6","gene_symbol":"AP003716.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67886477,"end":67906350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257038.1","gene_symbol":"AP002761.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73307235,"end":73309361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188763.4","gene_symbol":"FZD9","gene_name":"frizzled class receptor 9 [Source:HGNC Symbol;Acc:HGNC:4047]","synonyms":"FZD3,CD349","biotype":"protein_coding","ncbi_id":"8326","summary":" Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008]","start":73433783,"end":73436120,"strand":1,"description":"frizzled class receptor 9 [Source:HGNC Symbol;Acc:HGNC:4047]"}, {"versioned_ensembl_gene_id":"ENSG00000129680.15","gene_symbol":"MAP7D3","gene_name":"MAP7 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25742]","synonyms":"FLJ12649","biotype":"protein_coding","ncbi_id":"79649","summary":"The protein encoded by this gene belongs to the MAP7 (microtubule-associated protein 7) family. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Mar 2010]","start":136213220,"end":136256482,"strand":-1,"description":"MAP7 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25742]"}, {"versioned_ensembl_gene_id":"ENSG00000251516.1","gene_symbol":"AC098583.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22607501,"end":22611063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260368.1","gene_symbol":"AC027373.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":100913247,"end":100914388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242399.1","gene_symbol":"RPS20P23","gene_name":"ribosomal protein S20 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36146]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271089","summary":null,"start":100776512,"end":100776865,"strand":-1,"description":"ribosomal protein S20 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36146]"}, {"versioned_ensembl_gene_id":"ENSG00000110169.10","gene_symbol":"HPX","gene_name":"hemopexin [Source:HGNC Symbol;Acc:HGNC:5171]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3263","summary":"This gene encodes a plasma glycoprotein that binds heme with high affinity. The encoded protein is an acute phase protein that transports heme from the plasma to the liver and may be involved in protecting cells from oxidative stress. [provided by RefSeq, Apr 2009]","start":6431049,"end":6442617,"strand":-1,"description":"hemopexin [Source:HGNC Symbol;Acc:HGNC:5171]"}, {"versioned_ensembl_gene_id":"ENSG00000178952.10","gene_symbol":"TUFM","gene_name":"Tu translation elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12420]","synonyms":"EFTu,EF-TuMT","biotype":"protein_coding","ncbi_id":"7284","summary":"This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]","start":28842411,"end":28846408,"strand":-1,"description":"Tu translation elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12420]"}, {"versioned_ensembl_gene_id":"ENSG00000263528.7","gene_symbol":"IKBKE","gene_name":"inhibitor of nuclear factor kappa B kinase subunit epsilon [Source:HGNC Symbol;Acc:HGNC:14552]","synonyms":"IKK-i,KIAA0151,IKKE","biotype":"protein_coding","ncbi_id":"9641","summary":"IKBKE is a noncanonical I-kappa-B (see MIM 164008) kinase (IKK) that is essential for regulating antiviral signaling pathways. IKBKE has also been identified as a breast cancer (MIM 114480) oncogene and is amplified and overexpressed in over 30% of breast carcinomas and breast cancer cell lines (Hutti et al., 2009 [PubMed 19481526]).[supplied by OMIM, Oct 2009]","start":206470476,"end":206496889,"strand":1,"description":"inhibitor of nuclear factor kappa B kinase subunit epsilon [Source:HGNC Symbol;Acc:HGNC:14552]"}, {"versioned_ensembl_gene_id":"ENSG00000233987.1","gene_symbol":"AC106706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194705548,"end":194706964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231651.1","gene_symbol":"DLG3-AS1","gene_name":"DLG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40182]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873930","summary":null,"start":70452958,"end":70455994,"strand":-1,"description":"DLG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40182]"}, {"versioned_ensembl_gene_id":"ENSG00000176749.8","gene_symbol":"CDK5R1","gene_name":"cyclin dependent kinase 5 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:1775]","synonyms":"p35nck5a,p35,Nck5a","biotype":"protein_coding","ncbi_id":"8851","summary":"The protein encoded by this gene (p35) is a neuron-specific activator of cyclin-dependent kinase 5 (CDK5); the activation of CDK5 is required for proper development of the central nervous system. The p35 form of this protein is proteolytically cleaved by calpain, generating a p25 form. The cleavage of p35 into p25 results in relocalization of the protein from the cell periphery to nuclear and perinuclear regions. P25 deregulates CDK5 activity by prolonging its activation and changing its cellular location. The p25 form accumulates in the brain neurons of patients with Alzheimer's disease. This accumulation correlates with an increase in CDK5 kinase activity, and may lead to aberrantly phosphorylated forms of the microtubule-associated protein tau, which contributes to Alzheimer's disease. [provided by RefSeq, Jul 2008]","start":32486619,"end":32491256,"strand":1,"description":"cyclin dependent kinase 5 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:1775]"}, {"versioned_ensembl_gene_id":"ENSG00000065613.13","gene_symbol":"SLK","gene_name":"STE20 like kinase [Source:HGNC Symbol;Acc:HGNC:11088]","synonyms":"STK2,se20-9,KIAA0204","biotype":"protein_coding","ncbi_id":"9748","summary":null,"start":103967201,"end":104029233,"strand":1,"description":"STE20 like kinase [Source:HGNC Symbol;Acc:HGNC:11088]"}, {"versioned_ensembl_gene_id":"ENSG00000267895.1","gene_symbol":"AC063977.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51143826,"end":51144196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164961.15","gene_symbol":"WASHC5","gene_name":"WASH complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:28984]","synonyms":"SPG8,KIAA0196","biotype":"protein_coding","ncbi_id":"9897","summary":"This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq, Aug 2009]","start":125024260,"end":125091840,"strand":-1,"description":"WASH complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:28984]"}, {"versioned_ensembl_gene_id":"ENSG00000080822.16","gene_symbol":"CLDND1","gene_name":"claudin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1322]","synonyms":"C3orf4","biotype":"protein_coding","ncbi_id":"56650","summary":null,"start":98497912,"end":98523066,"strand":-1,"description":"claudin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1322]"}, {"versioned_ensembl_gene_id":"ENSG00000072818.11","gene_symbol":"ACAP1","gene_name":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 [Source:HGNC Symbol;Acc:HGNC:16467]","synonyms":"KIAA0050,CENTB1","biotype":"protein_coding","ncbi_id":"9744","summary":null,"start":7336529,"end":7351478,"strand":1,"description":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 [Source:HGNC Symbol;Acc:HGNC:16467]"}, {"versioned_ensembl_gene_id":"ENSG00000135953.10","gene_symbol":"MFSD9","gene_name":"major facilitator superfamily domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28158]","synonyms":"MGC11332","biotype":"protein_coding","ncbi_id":"84804","summary":null,"start":102715840,"end":102736888,"strand":-1,"description":"major facilitator superfamily domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28158]"}, {"versioned_ensembl_gene_id":"ENSG00000197938.5","gene_symbol":"OR5H2","gene_name":"olfactory receptor family 5 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:14752]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79310","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98282888,"end":98283832,"strand":1,"description":"olfactory receptor family 5 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:14752]"}, {"versioned_ensembl_gene_id":"ENSG00000253371.1","gene_symbol":"AC091096.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92500583,"end":92509816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253682.1","gene_symbol":"AC022695.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92403545,"end":92413645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265798.6","gene_symbol":"AC138207.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31038575,"end":31059121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237456.3","gene_symbol":"AC104849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62124204,"end":62124608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126861.4","gene_symbol":"OMG","gene_name":"oligodendrocyte myelin glycoprotein [Source:HGNC Symbol;Acc:HGNC:8135]","synonyms":"OMGP","biotype":"protein_coding","ncbi_id":"4974","summary":null,"start":31272013,"end":31297539,"strand":-1,"description":"oligodendrocyte myelin glycoprotein [Source:HGNC Symbol;Acc:HGNC:8135]"}, {"versioned_ensembl_gene_id":"ENSG00000230376.1","gene_symbol":"MEMO1P4","gene_name":"mediator of cell motility 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38504]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462785","summary":null,"start":123765301,"end":123765686,"strand":1,"description":"mediator of cell motility 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38504]"}, {"versioned_ensembl_gene_id":"ENSG00000233778.3","gene_symbol":"AC104339.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92144088,"end":92144435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282988.1","gene_symbol":"HIST1H3D","gene_name":"histone cluster 1 H3 family member d [Source:HGNC Symbol;Acc:HGNC:4767]","synonyms":"H3FB,H3/b,H3FB,H3/b","biotype":"protein_coding","ncbi_id":"8351","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26195595,"end":26199293,"strand":-1,"description":"histone cluster 1 H3 family member d [Source:HGNC Symbol;Acc:HGNC:4767]"}, {"versioned_ensembl_gene_id":"ENSG00000231647.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31581764,"end":31582598,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000138092.10","gene_symbol":"CENPO","gene_name":"centromere protein O [Source:HGNC Symbol;Acc:HGNC:28152]","synonyms":"CENP-O,MGC11266","biotype":"protein_coding","ncbi_id":"79172","summary":"This gene encodes a component of the interphase centromere complex. The encoded protein is localized to the centromere throughout the cell cycle and is required for bipolar spindle assembly, chromosome segregation and checkpoint signaling during mitosis. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":24793136,"end":24822376,"strand":1,"description":"centromere protein O [Source:HGNC Symbol;Acc:HGNC:28152]"}, {"versioned_ensembl_gene_id":"ENSG00000253431.1","gene_symbol":"SRPK2P","gene_name":"SRSF protein kinase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:30303]","synonyms":"SRPK2ps","biotype":"processed_pseudogene","ncbi_id":"100419416","summary":null,"start":62863082,"end":62864181,"strand":-1,"description":"SRSF protein kinase 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:30303]"}, {"versioned_ensembl_gene_id":"ENSG00000213070.3","gene_symbol":"HMGB3P6","gene_name":"high mobility group box 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39283]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729952","summary":null,"start":164356767,"end":164357364,"strand":1,"description":"high mobility group box 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39283]"}, {"versioned_ensembl_gene_id":"ENSG00000226978.1","gene_symbol":"MAGI2-AS2","gene_name":"MAGI2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40861]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874021","summary":null,"start":79008988,"end":79012277,"strand":1,"description":"MAGI2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40861]"}, {"versioned_ensembl_gene_id":"ENSG00000228165.1","gene_symbol":"AL158147.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4850299,"end":4850373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224981.1","gene_symbol":"AC000367.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126868767,"end":126870532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000024862.17","gene_symbol":"CCDC28A","gene_name":"coiled-coil domain containing 28A [Source:HGNC Symbol;Acc:HGNC:21098]","synonyms":"DKFZp586D0623,CCRL1AP,C6orf80","biotype":"protein_coding","ncbi_id":"25901","summary":"This gene encodes a coiled-coil domain containing protein. Although the specific function of this gene has not yet been determined, this gene is a known translocation partner of nucleoporin 98 in acute leukemias. The resulting fusion gene produces a nucleoporin 98-coiled-coil domain-containing protein 28A chimeric protein which may be involved in promoting myeloproliferative neoplasms. [provided by RefSeq, Jan 2017]","start":138773509,"end":138793319,"strand":1,"description":"coiled-coil domain containing 28A [Source:HGNC Symbol;Acc:HGNC:21098]"}, {"versioned_ensembl_gene_id":"ENSG00000238162.1","gene_symbol":"AC009237.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95485541,"end":95485805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233275.1","gene_symbol":"AC009238.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95434759,"end":95435113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077044.10","gene_symbol":"DGKD","gene_name":"diacylglycerol kinase delta [Source:HGNC Symbol;Acc:HGNC:2851]","synonyms":"KIAA0145,DGKdelta","biotype":"protein_coding","ncbi_id":"8527","summary":"This gene encodes a cytoplasmic enzyme that phosphorylates diacylglycerol to produce phosphatidic acid. Diacylglycerol and phosphatidic acid are two lipids that act as second messengers in signaling cascades. Their cellular concentrations are regulated by the encoded protein, and so it is thought to play an important role in cellular signal transduction. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":233354507,"end":233472104,"strand":1,"description":"diacylglycerol kinase delta [Source:HGNC Symbol;Acc:HGNC:2851]"}, {"versioned_ensembl_gene_id":"ENSG00000226855.1","gene_symbol":"RPSAP17","gene_name":"ribosomal protein SA pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35707]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270873","summary":null,"start":154378207,"end":154379089,"strand":-1,"description":"ribosomal protein SA pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35707]"}, {"versioned_ensembl_gene_id":"ENSG00000119508.17","gene_symbol":"NR4A3","gene_name":"nuclear receptor subfamily 4 group A member 3 [Source:HGNC Symbol;Acc:HGNC:7982]","synonyms":"CSMF,CHN,NOR1,MINOR","biotype":"protein_coding","ncbi_id":"8013","summary":"This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcriptional activator. The protein can efficiently bind the NGFI-B Response Element (NBRE). Three different versions of extraskeletal myxoid chondrosarcomas (EMCs) are the result of reciprocal translocations between this gene and other genes. The translocation breakpoints are associated with Nuclear Receptor Subfamily 4, Group A, Member 3 (on chromosome 9) and either Ewing Sarcome Breakpoint Region 1 (on chromosome 22), RNA Polymerase II, TATA Box-Binding Protein-Associated Factor, 68-KD (on chromosome 17), or Transcription factor 12 (on chromosome 15). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":99821855,"end":99866891,"strand":1,"description":"nuclear receptor subfamily 4 group A member 3 [Source:HGNC Symbol;Acc:HGNC:7982]"}, {"versioned_ensembl_gene_id":"ENSG00000215861.5","gene_symbol":"AC245297.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149197992,"end":149321732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274341.1","gene_symbol":"AC005899.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32408013,"end":32408309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251127.2","gene_symbol":"AC091173.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61759094,"end":61765969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238251.2","gene_symbol":"AL133477.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96407284,"end":96407797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175985.9","gene_symbol":"PLEKHD1","gene_name":"pleckstrin homology and coiled-coil domain containing D1 [Source:HGNC Symbol;Acc:HGNC:20148]","synonyms":"UPF0639","biotype":"protein_coding","ncbi_id":"400224","summary":null,"start":69484692,"end":69531551,"strand":1,"description":"pleckstrin homology and coiled-coil domain containing D1 [Source:HGNC Symbol;Acc:HGNC:20148]"}, {"versioned_ensembl_gene_id":"ENSG00000255558.1","gene_symbol":"AC013762.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13054615,"end":13134839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161202.17","gene_symbol":"DVL3","gene_name":"dishevelled segment polarity protein 3 [Source:HGNC Symbol;Acc:HGNC:3087]","synonyms":"KIAA0208","biotype":"protein_coding","ncbi_id":"1857","summary":"This gene is a member of a multi-gene family which shares strong similarity with the Drosophila dishevelled gene, dsh. The Drosophila dishevelled gene encodes a cytoplasmic phosphoprotein that regulates cell proliferation. [provided by RefSeq, Jul 2008]","start":184155388,"end":184173610,"strand":1,"description":"dishevelled segment polarity protein 3 [Source:HGNC Symbol;Acc:HGNC:3087]"}, {"versioned_ensembl_gene_id":"ENSG00000277092.4","gene_symbol":"LILRA4","gene_name":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]","synonyms":"CD85g,ILT7","biotype":"protein_coding","ncbi_id":"23547","summary":"This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015]","start":54341203,"end":54347168,"strand":-1,"description":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]"}, {"versioned_ensembl_gene_id":"ENSG00000246982.6","gene_symbol":"Z84485.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36146698,"end":36197205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124251.10","gene_symbol":"TP53TG5","gene_name":"TP53 target 5 [Source:HGNC Symbol;Acc:HGNC:15856]","synonyms":"dJ453C12.5,CLG01,C20orf10","biotype":"protein_coding","ncbi_id":"27296","summary":null,"start":45372563,"end":45407889,"strand":-1,"description":"TP53 target 5 [Source:HGNC Symbol;Acc:HGNC:15856]"}, {"versioned_ensembl_gene_id":"ENSG00000166106.3","gene_symbol":"ADAMTS15","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 15 [Source:HGNC Symbol;Acc:HGNC:16305]","synonyms":null,"biotype":"protein_coding","ncbi_id":"170689","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme, which may play a role in versican processing during skeletal muscle development. This gene may function as a tumor suppressor in colorectal and breast cancers. [provided by RefSeq, May 2016]","start":130448974,"end":130476641,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 15 [Source:HGNC Symbol;Acc:HGNC:16305]"}, {"versioned_ensembl_gene_id":"ENSG00000230171.1","gene_symbol":"RPL22P18","gene_name":"ribosomal protein L22 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36232]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271290","summary":null,"start":80125941,"end":80126317,"strand":1,"description":"ribosomal protein L22 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36232]"}, {"versioned_ensembl_gene_id":"ENSG00000171428.13","gene_symbol":"NAT1","gene_name":"N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:7645]","synonyms":"AAC1","biotype":"protein_coding","ncbi_id":"9","summary":"This gene is one of two arylamine N-acetyltransferase (NAT) genes in the human genome, and is orthologous to the mouse and rat Nat2 genes. The enzyme encoded by this gene catalyzes the transfer of an acetyl group from acetyl-CoA to various arylamine and hydrazine substrates. This enzyme helps metabolize drugs and other xenobiotics, and functions in folate catabolism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":18170477,"end":18223689,"strand":1,"description":"N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:7645]"}, {"versioned_ensembl_gene_id":"ENSG00000253937.1","gene_symbol":"NATP","gene_name":"N-acetyltransferase pseudogene [Source:HGNC Symbol;Acc:HGNC:15]","synonyms":"NATP1,AACP","biotype":"unprocessed_pseudogene","ncbi_id":"11","summary":null,"start":18370607,"end":18371484,"strand":1,"description":"N-acetyltransferase pseudogene [Source:HGNC Symbol;Acc:HGNC:15]"}, {"versioned_ensembl_gene_id":"ENSG00000090932.10","gene_symbol":"DLL3","gene_name":"delta like canonical Notch ligand 3 [Source:HGNC Symbol;Acc:HGNC:2909]","synonyms":"SCDO1","biotype":"protein_coding","ncbi_id":"10683","summary":"This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":39498895,"end":39508481,"strand":1,"description":"delta like canonical Notch ligand 3 [Source:HGNC Symbol;Acc:HGNC:2909]"}, {"versioned_ensembl_gene_id":"ENSG00000105662.15","gene_symbol":"CRTC1","gene_name":"CREB regulated transcription coactivator 1 [Source:HGNC Symbol;Acc:HGNC:16062]","synonyms":"TORC1,MECT1,KIAA0616,FLJ14027","biotype":"protein_coding","ncbi_id":"23373","summary":null,"start":18683677,"end":18782333,"strand":1,"description":"CREB regulated transcription coactivator 1 [Source:HGNC Symbol;Acc:HGNC:16062]"}, {"versioned_ensembl_gene_id":"ENSG00000269556.7","gene_symbol":"TMEM185A","gene_name":"transmembrane protein 185A [Source:HGNC Symbol;Acc:HGNC:17125]","synonyms":"FRAXF,FAM11A,CXorf13","biotype":"protein_coding","ncbi_id":"84548","summary":"The protein encoded by this gene is predicted to be a transmembrane protein. This gene is best known for localizing to the CpG island of the fragile site FRAXF. The 5' untranslated region of this gene contains a CGG trinucleotide repeat sequence that normally consists of 7-40 tandem CGG repeats but which can expand to greater than 300 repeats. Methylation of the CpG island leads to transcriptional silencing of this gene, but neither the silencing nor an expanded repeat region appear to manifest itself in a clear phenotypic manner. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Aug 2013]","start":149596556,"end":149631912,"strand":-1,"description":"transmembrane protein 185A [Source:HGNC Symbol;Acc:HGNC:17125]"}, {"versioned_ensembl_gene_id":"ENSG00000232807.2","gene_symbol":"AL137186.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5934270,"end":5945900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187079.16","gene_symbol":"TEAD1","gene_name":"TEA domain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:11714]","synonyms":"TEF-1,TCF13,AA","biotype":"protein_coding","ncbi_id":"7003","summary":"This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified. [provided by RefSeq, May 2010]","start":12674591,"end":12944483,"strand":1,"description":"TEA domain transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:11714]"}, {"versioned_ensembl_gene_id":"ENSG00000226785.1","gene_symbol":"AC068599.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34383788,"end":34635340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138459.8","gene_symbol":"SLC35A5","gene_name":"solute carrier family 35 member A5 [Source:HGNC Symbol;Acc:HGNC:20792]","synonyms":"FLJ20730","biotype":"protein_coding","ncbi_id":"55032","summary":"This gene encodes a transmembrane protein which belongs to subfamily 35A of the solute carrier superfamily. The encoded protein is a nucleoside-sugar transporter. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":112561709,"end":112585577,"strand":1,"description":"solute carrier family 35 member A5 [Source:HGNC Symbol;Acc:HGNC:20792]"}, {"versioned_ensembl_gene_id":"ENSG00000163689.19","gene_symbol":"C3orf67","gene_name":"chromosome 3 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:24763]","synonyms":"FLJ42930,FLJ42117","biotype":"protein_coding","ncbi_id":"200844","summary":null,"start":58717365,"end":59050084,"strand":-1,"description":"chromosome 3 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:24763]"}, {"versioned_ensembl_gene_id":"ENSG00000272662.1","gene_symbol":"AC073352.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119497678,"end":119498181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118849.9","gene_symbol":"RARRES1","gene_name":"retinoic acid receptor responder 1 [Source:HGNC Symbol;Acc:HGNC:9867]","synonyms":"TIG1,LXNL","biotype":"protein_coding","ncbi_id":"5918","summary":"This gene was identified as a retinoid acid (RA) receptor-responsive gene. It encodes a type 1 membrane protein. The expression of this gene is upregulated by tazarotene as well as by retinoic acid receptors. The expression of this gene is found to be downregulated in prostate cancer, which is caused by the methylation of its promoter and CpG island. Alternatively spliced transcript variant encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":158696892,"end":158732696,"strand":-1,"description":"retinoic acid receptor responder 1 [Source:HGNC Symbol;Acc:HGNC:9867]"}, {"versioned_ensembl_gene_id":"ENSG00000156414.18","gene_symbol":"TDRD9","gene_name":"tudor domain containing 9 [Source:HGNC Symbol;Acc:HGNC:20122]","synonyms":"NET54,FLJ36164,DKFZp434N0820,C14orf75","biotype":"protein_coding","ncbi_id":"122402","summary":null,"start":103928462,"end":104052667,"strand":1,"description":"tudor domain containing 9 [Source:HGNC Symbol;Acc:HGNC:20122]"}, {"versioned_ensembl_gene_id":"ENSG00000239528.1","gene_symbol":"RPS14P8","gene_name":"ribosomal protein S14 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37027]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644146","summary":null,"start":116562562,"end":116562930,"strand":1,"description":"ribosomal protein S14 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37027]"}, {"versioned_ensembl_gene_id":"ENSG00000251040.1","gene_symbol":"LINC02480","gene_name":"long intergenic non-protein coding RNA 2480 [Source:HGNC Symbol;Acc:HGNC:53454]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377652","summary":null,"start":52044805,"end":52046954,"strand":1,"description":"long intergenic non-protein coding RNA 2480 [Source:HGNC Symbol;Acc:HGNC:53454]"}, {"versioned_ensembl_gene_id":"ENSG00000130726.11","gene_symbol":"TRIM28","gene_name":"tripartite motif containing 28 [Source:HGNC Symbol;Acc:HGNC:16384]","synonyms":"KAP1,TIF1B,TF1B,RNF96,PPP1R157","biotype":"protein_coding","ncbi_id":"10155","summary":"The protein encoded by this gene mediates transcriptional control by interaction with the Kruppel-associated box repression domain found in many transcription factors. The protein localizes to the nucleus and is thought to associate with specific chromatin regions. The protein is a member of the tripartite motif family. This tripartite motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]","start":58544091,"end":58550722,"strand":1,"description":"tripartite motif containing 28 [Source:HGNC Symbol;Acc:HGNC:16384]"}, {"versioned_ensembl_gene_id":"ENSG00000270997.1","gene_symbol":"AC073137.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113415689,"end":113416322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278894.1","gene_symbol":"AC073348.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":113451072,"end":113451402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243675.1","gene_symbol":"AC080013.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158763431,"end":158763753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000029364.11","gene_symbol":"SLC39A9","gene_name":"solute carrier family 39 member 9 [Source:HGNC Symbol;Acc:HGNC:20182]","synonyms":"FLJ11274","biotype":"protein_coding","ncbi_id":"55334","summary":null,"start":69398015,"end":69462388,"strand":1,"description":"solute carrier family 39 member 9 [Source:HGNC Symbol;Acc:HGNC:20182]"}, {"versioned_ensembl_gene_id":"ENSG00000240207.6","gene_symbol":"AC080013.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158732263,"end":158784070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249167.1","gene_symbol":"SEMA6A-AS2","gene_name":"SEMA6A antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:52754]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379132","summary":null,"start":116574482,"end":116591398,"strand":1,"description":"SEMA6A antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:52754]"}, {"versioned_ensembl_gene_id":"ENSG00000186583.11","gene_symbol":"SPATC1","gene_name":"spermatogenesis and centriole associated 1 [Source:HGNC Symbol;Acc:HGNC:30510]","synonyms":"SPERIOLIN,SPATA15,MGC61633","biotype":"protein_coding","ncbi_id":"375686","summary":null,"start":144012414,"end":144047085,"strand":1,"description":"spermatogenesis and centriole associated 1 [Source:HGNC Symbol;Acc:HGNC:30510]"}, {"versioned_ensembl_gene_id":"ENSG00000248445.5","gene_symbol":"SEMA6A-AS1","gene_name":"SEMA6A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51110]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927233","summary":null,"start":116447547,"end":116508276,"strand":1,"description":"SEMA6A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51110]"}, {"versioned_ensembl_gene_id":"ENSG00000001036.13","gene_symbol":"FUCA2","gene_name":"fucosidase, alpha-L- 2, plasma [Source:HGNC Symbol;Acc:HGNC:4008]","synonyms":"MGC1314,dJ20N2.5","biotype":"protein_coding","ncbi_id":"2519","summary":"This gene encodes a plasma alpha-L-fucosidase, which represents 10-20% of the total cellular fucosidase activity. The protein is a member of the glycosyl hydrolase 29 family, and catalyzes the hydrolysis of the alpha-1,6-linked fucose joined to the reducing-end N-acetylglucosamine of the carbohydrate moieties of glycoproteins. This enzyme is essential for Helicobacter pylori adhesion to human gastric cancer cells. [provided by RefSeq, Aug 2010]","start":143494811,"end":143511690,"strand":-1,"description":"fucosidase, alpha-L- 2, plasma [Source:HGNC Symbol;Acc:HGNC:4008]"}, {"versioned_ensembl_gene_id":"ENSG00000198734.10","gene_symbol":"F5","gene_name":"coagulation factor V [Source:HGNC Symbol;Acc:HGNC:3542]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2153","summary":"This gene encodes an essential cofactor of the blood coagulation cascade. This factor circulates in plasma, and is converted to the active form by the release of the activation peptide by thrombin during coagulation. This generates a heavy chain and a light chain which are held together by calcium ions. The activated protein is a cofactor that participates with activated coagulation factor X to activate prothrombin to thrombin. Defects in this gene result in either an autosomal recessive hemorrhagic diathesis or an autosomal dominant form of thrombophilia, which is known as activated protein C resistance. [provided by RefSeq, Oct 2008]","start":169514166,"end":169586588,"strand":-1,"description":"coagulation factor V [Source:HGNC Symbol;Acc:HGNC:3542]"}, {"versioned_ensembl_gene_id":"ENSG00000260473.2","gene_symbol":"AC068987.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51815043,"end":51842106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221916.3","gene_symbol":"C19orf73","gene_name":"chromosome 19 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:25534]","synonyms":"FLJ10490","biotype":"protein_coding","ncbi_id":"55150","summary":null,"start":49118397,"end":49119140,"strand":-1,"description":"chromosome 19 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:25534]"}, {"versioned_ensembl_gene_id":"ENSG00000254416.5","gene_symbol":"AP000924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110355130,"end":110406400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232937.1","gene_symbol":"AL589765.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":151765709,"end":151766389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159905.14","gene_symbol":"ZNF221","gene_name":"zinc finger protein 221 [Source:HGNC Symbol;Acc:HGNC:13014]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7638","summary":null,"start":43951223,"end":43967709,"strand":1,"description":"zinc finger protein 221 [Source:HGNC Symbol;Acc:HGNC:13014]"}, {"versioned_ensembl_gene_id":"ENSG00000276779.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803599,"end":54814548,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000259562.2","gene_symbol":"AC090607.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":78290527,"end":78291221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230006.7","gene_symbol":"ANKRD36BP2","gene_name":"ankyrin repeat domain 36B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33607]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645784","summary":null,"start":88765807,"end":88806612,"strand":1,"description":"ankyrin repeat domain 36B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33607]"}, {"versioned_ensembl_gene_id":"ENSG00000276976.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54638174,"end":54643363,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000273576.1","gene_symbol":"AC009283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39566915,"end":39567559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182134.15","gene_symbol":"TDRKH","gene_name":"tudor and KH domain containing [Source:HGNC Symbol;Acc:HGNC:11713]","synonyms":"TDRD2","biotype":"protein_coding","ncbi_id":"11022","summary":null,"start":151770107,"end":151791416,"strand":-1,"description":"tudor and KH domain containing [Source:HGNC Symbol;Acc:HGNC:11713]"}, {"versioned_ensembl_gene_id":"ENSG00000163449.10","gene_symbol":"TMEM169","gene_name":"transmembrane protein 169 [Source:HGNC Symbol;Acc:HGNC:25130]","synonyms":"FLJ34263","biotype":"protein_coding","ncbi_id":"92691","summary":null,"start":216081866,"end":216102783,"strand":1,"description":"transmembrane protein 169 [Source:HGNC Symbol;Acc:HGNC:25130]"}, {"versioned_ensembl_gene_id":"ENSG00000108798.8","gene_symbol":"ABI3","gene_name":"ABI family member 3 [Source:HGNC Symbol;Acc:HGNC:29859]","synonyms":"SSH3BP3,NESH","biotype":"protein_coding","ncbi_id":"51225","summary":"This gene encodes a member of an adaptor protein family. Members of this family encode proteins containing a homeobox homology domain, proline rich region and Src-homology 3 (SH3) domain, and are components of the Abi/WAVE complex which regulates actin polymerization. The encoded protein inhibits ectopic metastasis of tumor cells as well as cell migration. This may be accomplished through interaction with p21-activated kinase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":49210227,"end":49223225,"strand":1,"description":"ABI family member 3 [Source:HGNC Symbol;Acc:HGNC:29859]"}, {"versioned_ensembl_gene_id":"ENSG00000237529.1","gene_symbol":"AL137847.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83276376,"end":83279499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172159.15","gene_symbol":"FRMD3","gene_name":"FERM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24125]","synonyms":"MGC20553,EPB41L4O","biotype":"protein_coding","ncbi_id":"257019","summary":"The protein encoded by this gene is a single pass membrane protein primarily found in ovaries. A similar protein in erythrocytes helps determine the shape of red blood cells, but the function of the encoded protein has not been determined. There is some evidence that this is a tumor suppressor gene, and there is also evidence linking defects in this gene to susceptibility to diabetic nephropathy in type 1 diabetes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":83242990,"end":83538546,"strand":-1,"description":"FERM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24125]"}, {"versioned_ensembl_gene_id":"ENSG00000259186.1","gene_symbol":"AC009660.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73483196,"end":73483943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278945.1","gene_symbol":"AP000770.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":116609995,"end":116610094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236437.1","gene_symbol":"LINC02151","gene_name":"long intergenic non-protein coding RNA 2151 [Source:HGNC Symbol;Acc:HGNC:53013]","synonyms":"TCONS_00019174","biotype":"lincRNA","ncbi_id":"109729162","summary":null,"start":116496899,"end":116500630,"strand":-1,"description":"long intergenic non-protein coding RNA 2151 [Source:HGNC Symbol;Acc:HGNC:53013]"}, {"versioned_ensembl_gene_id":"ENSG00000104983.8","gene_symbol":"CCDC61","gene_name":"coiled-coil domain containing 61 [Source:HGNC Symbol;Acc:HGNC:33629]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729440","summary":null,"start":45995461,"end":46021318,"strand":1,"description":"coiled-coil domain containing 61 [Source:HGNC Symbol;Acc:HGNC:33629]"}, {"versioned_ensembl_gene_id":"ENSG00000162032.15","gene_symbol":"SPSB3","gene_name":"splA/ryanodine receptor domain and SOCS box containing 3 [Source:HGNC Symbol;Acc:HGNC:30629]","synonyms":"SSB-3,C16orf31","biotype":"protein_coding","ncbi_id":"90864","summary":null,"start":1776712,"end":1793700,"strand":-1,"description":"splA/ryanodine receptor domain and SOCS box containing 3 [Source:HGNC Symbol;Acc:HGNC:30629]"}, {"versioned_ensembl_gene_id":"ENSG00000113209.8","gene_symbol":"PCDHB5","gene_name":"protocadherin beta 5 [Source:HGNC Symbol;Acc:HGNC:8690]","synonyms":"PCDH-BETA5,DKFZp586B0217","biotype":"protein_coding","ncbi_id":"26167","summary":"This gene is a member of the protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. [provided by RefSeq, Jul 2008]","start":141135218,"end":141138625,"strand":1,"description":"protocadherin beta 5 [Source:HGNC Symbol;Acc:HGNC:8690]"}, {"versioned_ensembl_gene_id":"ENSG00000268655.2","gene_symbol":"AC008687.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49017496,"end":49020523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279472.1","gene_symbol":"AC244517.8","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":141177849,"end":141182369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011465.16","gene_symbol":"DCN","gene_name":"decorin [Source:HGNC Symbol;Acc:HGNC:2705]","synonyms":"SLRR1B,DSPG2","biotype":"protein_coding","ncbi_id":"1634","summary":"This gene encodes a member of the small leucine-rich proteoglycan family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. This protein plays a role in collagen fibril assembly. Binding of this protein to multiple cell surface receptors mediates its role in tumor suppression, including a stimulatory effect on autophagy and inflammation and an inhibitory effect on angiogenesis and tumorigenesis. This gene and the related gene biglycan are thought to be the result of a gene duplication. Mutations in this gene are associated with congenital stromal corneal dystrophy in human patients. [provided by RefSeq, Nov 2015]","start":91140484,"end":91183123,"strand":-1,"description":"decorin [Source:HGNC Symbol;Acc:HGNC:2705]"}, {"versioned_ensembl_gene_id":"ENSG00000231863.1","gene_symbol":"AL139393.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160931080,"end":160969771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268460.1","gene_symbol":"AC006262.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46203426,"end":46214837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132694.18","gene_symbol":"ARHGEF11","gene_name":"Rho guanine nucleotide exchange factor 11 [Source:HGNC Symbol;Acc:HGNC:14580]","synonyms":"PDZ-RHOGEF,KIAA0380,GTRAP48","biotype":"protein_coding","ncbi_id":"9826","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form a complex with G proteins and stimulate Rho-dependent signals. A similar protein in rat interacts with glutamate transporter EAAT4 and modulates its glutamate transport activity. Expression of the rat protein induces the reorganization of the actin cytoskeleton and its overexpression induces the formation of membrane ruffling and filopodia. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":156934840,"end":157045370,"strand":-1,"description":"Rho guanine nucleotide exchange factor 11 [Source:HGNC Symbol;Acc:HGNC:14580]"}, {"versioned_ensembl_gene_id":"ENSG00000282997.1","gene_symbol":"AL162456.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":91994518,"end":91996523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240995.2","gene_symbol":"AC069454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49148339,"end":49149111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256281.1","gene_symbol":"AP003174.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115532322,"end":115532953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267922.1","gene_symbol":"AC007785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46101122,"end":46196218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167080.8","gene_symbol":"B4GALNT2","gene_name":"beta-1,4-N-acetyl-galactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:24136]","synonyms":"Sda,GALGT2,Cad","biotype":"protein_coding","ncbi_id":"124872","summary":"B4GALNT2 catalyzes the last step in the biosynthesis of the human Sd(a) antigen through the addition of an N-acetylgalactosamine residue via a beta-1,4 linkage to a subterminal galactose residue substituted with an alpha-2,3-linked sialic acid. B4GALNT2 also catalyzes the last step in the biosynthesis of the Cad antigen (Montiel et al., 2003 [PubMed 12678917]).[supplied by OMIM, Mar 2008]","start":49132460,"end":49176840,"strand":1,"description":"beta-1,4-N-acetyl-galactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:24136]"}, {"versioned_ensembl_gene_id":"ENSG00000204869.8","gene_symbol":"IGFL4","gene_name":"IGF like family member 4 [Source:HGNC Symbol;Acc:HGNC:32931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"444882","summary":null,"start":46039748,"end":46077118,"strand":-1,"description":"IGF like family member 4 [Source:HGNC Symbol;Acc:HGNC:32931]"}, {"versioned_ensembl_gene_id":"ENSG00000248724.6","gene_symbol":"NPHP3-AS1","gene_name":"NPHP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24129]","synonyms":"NCRNA00119","biotype":"antisense_RNA","ncbi_id":"348808","summary":null,"start":132721750,"end":132874223,"strand":1,"description":"NPHP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24129]"}, {"versioned_ensembl_gene_id":"ENSG00000035681.7","gene_symbol":"NSMAF","gene_name":"neutral sphingomyelinase activation associated factor [Source:HGNC Symbol;Acc:HGNC:8017]","synonyms":"GRAMD5,FAN","biotype":"protein_coding","ncbi_id":"8439","summary":"This gene encodes a WD-repeat protein that binds the cytoplasmic sphingomyelinase activation domain of the 55kD tumor necrosis factor receptor. This protein is required for TNF-mediated activation of neutral sphingomyelinase and may play a role in regulating TNF-induced cellular responses such as inflammation. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2009]","start":58583504,"end":58659844,"strand":-1,"description":"neutral sphingomyelinase activation associated factor [Source:HGNC Symbol;Acc:HGNC:8017]"}, {"versioned_ensembl_gene_id":"ENSG00000278978.1","gene_symbol":"AC092611.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":151669786,"end":151670503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064787.13","gene_symbol":"BCAS1","gene_name":"breast carcinoma amplified sequence 1 [Source:HGNC Symbol;Acc:HGNC:974]","synonyms":"NABC1,AIBC1","biotype":"protein_coding","ncbi_id":"8537","summary":"This gene resides in a region at 20q13 which is amplified in a variety of tumor types and associated with more aggressive tumor phenotypes. Among the genes identified from this region, it was found to be highly expressed in three amplified breast cancer cell lines and in one breast tumor without amplification at 20q13.2. However, this gene is not in the common region of maximal amplification and its expression was not detected in the breast cancer cell line MCF7, in which this region is highly amplified. Although not consistently expressed, this gene is a candidate oncogene. [provided by RefSeq, Apr 2016]","start":53936777,"end":54070594,"strand":-1,"description":"breast carcinoma amplified sequence 1 [Source:HGNC Symbol;Acc:HGNC:974]"}, {"versioned_ensembl_gene_id":"ENSG00000119599.16","gene_symbol":"DCAF4","gene_name":"DDB1 and CUL4 associated factor 4 [Source:HGNC Symbol;Acc:HGNC:20229]","synonyms":"WDR21A,WDR21,DKFZp434K114","biotype":"protein_coding","ncbi_id":"26094","summary":"This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2009]","start":72926332,"end":72959703,"strand":1,"description":"DDB1 and CUL4 associated factor 4 [Source:HGNC Symbol;Acc:HGNC:20229]"}, {"versioned_ensembl_gene_id":"ENSG00000268401.1","gene_symbol":"AC007785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46027654,"end":46030161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139405.15","gene_symbol":"RITA1","gene_name":"RBPJ interacting and tubulin associated 1 [Source:HGNC Symbol;Acc:HGNC:25925]","synonyms":"RITA,FLJ14827,C12orf52","biotype":"protein_coding","ncbi_id":"84934","summary":null,"start":113185526,"end":113192368,"strand":1,"description":"RBPJ interacting and tubulin associated 1 [Source:HGNC Symbol;Acc:HGNC:25925]"}, {"versioned_ensembl_gene_id":"ENSG00000225563.1","gene_symbol":"AC006076.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53799823,"end":53801318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257957.1","gene_symbol":"QRSL1P3","gene_name":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43669]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422374","summary":null,"start":35765795,"end":35767110,"strand":1,"description":"glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43669]"}, {"versioned_ensembl_gene_id":"ENSG00000148341.17","gene_symbol":"SH3GLB2","gene_name":"SH3 domain containing GRB2 like, endophilin B2 [Source:HGNC Symbol;Acc:HGNC:10834]","synonyms":"KIAA1848","biotype":"protein_coding","ncbi_id":"56904","summary":null,"start":129007036,"end":129028303,"strand":-1,"description":"SH3 domain containing GRB2 like, endophilin B2 [Source:HGNC Symbol;Acc:HGNC:10834]"}, {"versioned_ensembl_gene_id":"ENSG00000181007.8","gene_symbol":"ZFP82","gene_name":"ZFP82 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:28682]","synonyms":"ZNF545,MGC45380,KIAA1948","biotype":"protein_coding","ncbi_id":"284406","summary":null,"start":36383120,"end":36418656,"strand":-1,"description":"ZFP82 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:28682]"}, {"versioned_ensembl_gene_id":"ENSG00000279399.1","gene_symbol":"AL356095.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80091411,"end":80091867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186615.10","gene_symbol":"KTN1-AS1","gene_name":"KTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19842]","synonyms":"C14orf33,MYCLo-3","biotype":"antisense_RNA","ncbi_id":"100129075","summary":null,"start":55499278,"end":55580110,"strand":-1,"description":"KTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19842]"}, {"versioned_ensembl_gene_id":"ENSG00000170629.14","gene_symbol":"DPY19L2P2","gene_name":"DPY19L2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21764]","synonyms":"FLJ36166,DKFZp434E092","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"349152","summary":null,"start":103175133,"end":103280410,"strand":-1,"description":"DPY19L2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21764]"}, {"versioned_ensembl_gene_id":"ENSG00000230091.6","gene_symbol":"TMEM254-AS1","gene_name":"TMEM254 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27340]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"219347","summary":null,"start":80046860,"end":80078912,"strand":-1,"description":"TMEM254 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27340]"}, {"versioned_ensembl_gene_id":"ENSG00000228948.2","gene_symbol":"SLC25A6P5","gene_name":"solute carrier family 25 member 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43854]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129319","summary":null,"start":105849710,"end":105851425,"strand":1,"description":"solute carrier family 25 member 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43854]"}, {"versioned_ensembl_gene_id":"ENSG00000123416.15","gene_symbol":"TUBA1B","gene_name":"tubulin alpha 1b [Source:HGNC Symbol;Acc:HGNC:18809]","synonyms":"K-ALPHA-1","biotype":"protein_coding","ncbi_id":"10376","summary":null,"start":49127782,"end":49131397,"strand":-1,"description":"tubulin alpha 1b [Source:HGNC Symbol;Acc:HGNC:18809]"}, {"versioned_ensembl_gene_id":"ENSG00000233672.6","gene_symbol":"RNASEH2B-AS1","gene_name":"RNASEH2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39967]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874255","summary":null,"start":50862172,"end":50910764,"strand":-1,"description":"RNASEH2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39967]"}, {"versioned_ensembl_gene_id":"ENSG00000019102.11","gene_symbol":"VSIG2","gene_name":"V-set and immunoglobulin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17149]","synonyms":"CTXL,CTH","biotype":"protein_coding","ncbi_id":"23584","summary":null,"start":124747472,"end":124752238,"strand":-1,"description":"V-set and immunoglobulin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17149]"}, {"versioned_ensembl_gene_id":"ENSG00000235879.1","gene_symbol":"FAR1P1","gene_name":"fatty acyl-CoA reductase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39675]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128011","summary":null,"start":90170866,"end":90171799,"strand":1,"description":"fatty acyl-CoA reductase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39675]"}, {"versioned_ensembl_gene_id":"ENSG00000270634.1","gene_symbol":"AC005518.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147704294,"end":147704575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118307.18","gene_symbol":"CASC1","gene_name":"cancer susceptibility 1 [Source:HGNC Symbol;Acc:HGNC:29599]","synonyms":"PPP1R54,LAS1,FLJ10921","biotype":"protein_coding","ncbi_id":"55259","summary":null,"start":25108420,"end":25195162,"strand":-1,"description":"cancer susceptibility 1 [Source:HGNC Symbol;Acc:HGNC:29599]"}, {"versioned_ensembl_gene_id":"ENSG00000023516.8","gene_symbol":"AKAP11","gene_name":"A-kinase anchoring protein 11 [Source:HGNC Symbol;Acc:HGNC:369]","synonyms":"KIAA0629,FLJ11304,DKFZp781I12161,AKAP220,PRKA11,PPP1R44","biotype":"protein_coding","ncbi_id":"11215","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is expressed at high levels throughout spermatogenesis and in mature sperm. It binds the RI and RII subunits of PKA in testis. It may serve a function in cell cycle control of both somatic cells and germ cells in addition to its putative role in spermatogenesis and sperm function. [provided by RefSeq, Jul 2008]","start":42272153,"end":42323267,"strand":1,"description":"A-kinase anchoring protein 11 [Source:HGNC Symbol;Acc:HGNC:369]"}, {"versioned_ensembl_gene_id":"ENSG00000197191.4","gene_symbol":"CYSRT1","gene_name":"cysteine rich tail 1 [Source:HGNC Symbol;Acc:HGNC:30529]","synonyms":"MGC59937,C9orf169","biotype":"protein_coding","ncbi_id":"375791","summary":null,"start":137224635,"end":137226311,"strand":1,"description":"cysteine rich tail 1 [Source:HGNC Symbol;Acc:HGNC:30529]"}, {"versioned_ensembl_gene_id":"ENSG00000259138.1","gene_symbol":"AL049780.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75127153,"end":75136930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180769.8","gene_symbol":"WDFY3-AS2","gene_name":"WDFY3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:21603]","synonyms":"NCRNA00247,FBI4,C4orf12","biotype":"processed_transcript","ncbi_id":"404201","summary":null,"start":84965682,"end":85011277,"strand":1,"description":"WDFY3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:21603]"}, {"versioned_ensembl_gene_id":"ENSG00000235770.5","gene_symbol":"LINC00607","gene_name":"long intergenic non-protein coding RNA 607 [Source:HGNC Symbol;Acc:HGNC:43944]","synonyms":null,"biotype":"lincRNA","ncbi_id":"646324","summary":null,"start":215611563,"end":215843722,"strand":-1,"description":"long intergenic non-protein coding RNA 607 [Source:HGNC Symbol;Acc:HGNC:43944]"}, {"versioned_ensembl_gene_id":"ENSG00000230838.1","gene_symbol":"LINC01614","gene_name":"long intergenic non-protein coding RNA 1614 [Source:HGNC Symbol;Acc:HGNC:51847]","synonyms":"TCONS_00003105,LCAL4","biotype":"lincRNA","ncbi_id":"105373869","summary":null,"start":215718043,"end":215719424,"strand":1,"description":"long intergenic non-protein coding RNA 1614 [Source:HGNC Symbol;Acc:HGNC:51847]"}, {"versioned_ensembl_gene_id":"ENSG00000150977.10","gene_symbol":"RILPL2","gene_name":"Rab interacting lysosomal protein like 2 [Source:HGNC Symbol;Acc:HGNC:28787]","synonyms":"FLJ32372,FLJ30380,MGC7036","biotype":"protein_coding","ncbi_id":"196383","summary":"This gene encodes a protein that contains a rab-interacting lysosomal protein-like domain. This protein may be involved in regulating lysosome morphology. This protein may also be a target for the Hepatitis C virus and assist in viral replication. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":123410683,"end":123436717,"strand":-1,"description":"Rab interacting lysosomal protein like 2 [Source:HGNC Symbol;Acc:HGNC:28787]"}, {"versioned_ensembl_gene_id":"ENSG00000229862.5","gene_symbol":"AL121972.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73523618,"end":73570596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278238.1","gene_symbol":"AL359513.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52454775,"end":52455331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246095.2","gene_symbol":"LINC01096","gene_name":"long intergenic non-protein coding RNA 1096 [Source:HGNC Symbol;Acc:HGNC:27739]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285548","summary":null,"start":13546075,"end":13547801,"strand":-1,"description":"long intergenic non-protein coding RNA 1096 [Source:HGNC Symbol;Acc:HGNC:27739]"}, {"versioned_ensembl_gene_id":"ENSG00000170348.8","gene_symbol":"TMED10","gene_name":"transmembrane p24 trafficking protein 10 [Source:HGNC Symbol;Acc:HGNC:16998]","synonyms":"P24(DELTA),p23,TMP21,p24delta1,p24d1","biotype":"protein_coding","ncbi_id":"10972","summary":"This gene is a member of the EMP24/GP25L/p24 family and encodes a protein with a GOLD domain. This type I membrane protein is localized to the plasma membrane and golgi cisternae and is involved in vesicular protein trafficking. The protein is also a member of a heteromeric secretase complex and regulates the complex's gamma-secretase activity without affecting its epsilon-secretase activity. Mutations in this gene have been associated with early-onset familial Alzheimer's disease. This gene has a pseudogene on chromosome 8. [provided by RefSeq, Jul 2008]","start":75131470,"end":75176631,"strand":-1,"description":"transmembrane p24 trafficking protein 10 [Source:HGNC Symbol;Acc:HGNC:16998]"}, {"versioned_ensembl_gene_id":"ENSG00000281202.2","gene_symbol":"LINC01097","gene_name":"long intergenic non-protein coding RNA 1097 [Source:HGNC Symbol;Acc:HGNC:27738]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285547","summary":null,"start":13526319,"end":13534335,"strand":-1,"description":"long intergenic non-protein coding RNA 1097 [Source:HGNC Symbol;Acc:HGNC:27738]"}, {"versioned_ensembl_gene_id":"ENSG00000274192.1","gene_symbol":"ABCB10P4","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132289","summary":null,"start":28518244,"end":28520426,"strand":-1,"description":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]"}, {"versioned_ensembl_gene_id":"ENSG00000270977.1","gene_symbol":"AC015849.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35893707,"end":35911023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215381.3","gene_symbol":"AL109936.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23244765,"end":23245224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101306.10","gene_symbol":"MYLK2","gene_name":"myosin light chain kinase 2 [Source:HGNC Symbol;Acc:HGNC:16243]","synonyms":"KMLC,skMLCK,MLCK2","biotype":"protein_coding","ncbi_id":"85366","summary":"This gene encodes a myosin light chain kinase, a calcium/calmodulin dependent enzyme, that is exclusively expressed in adult skeletal muscle. [provided by RefSeq, Jul 2008]","start":31819308,"end":31834689,"strand":1,"description":"myosin light chain kinase 2 [Source:HGNC Symbol;Acc:HGNC:16243]"}, {"versioned_ensembl_gene_id":"ENSG00000282621.1","gene_symbol":"TRBV19","gene_name":"T-cell receptor beta variable 19 [Source:HGNC Symbol;Acc:HGNC:12194]","synonyms":"TCRBV19S1,TCRBV17S1A1T","biotype":"TR_V_gene","ncbi_id":"28568","summary":null,"start":142660632,"end":142661315,"strand":1,"description":"T-cell receptor beta variable 19 [Source:HGNC Symbol;Acc:HGNC:12194]"}, {"versioned_ensembl_gene_id":"ENSG00000182397.14","gene_symbol":"DNM1P46","gene_name":"dynamin 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:35199]","synonyms":"FLJ45937,DNM1DN14@,DNM1DN14.2,DKFZp434I1020,C15orf51","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"196968","summary":null,"start":99790156,"end":99806927,"strand":-1,"description":"dynamin 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:35199]"}, {"versioned_ensembl_gene_id":"ENSG00000250888.1","gene_symbol":"LINC01455","gene_name":"long intergenic non-protein coding RNA 1455 [Source:HGNC Symbol;Acc:HGNC:50545]","synonyms":"TCONS_00009433,MDONA","biotype":"antisense_RNA","ncbi_id":"105616916","summary":null,"start":79936579,"end":79967626,"strand":1,"description":"long intergenic non-protein coding RNA 1455 [Source:HGNC Symbol;Acc:HGNC:50545]"}, {"versioned_ensembl_gene_id":"ENSG00000250208.6","gene_symbol":"FZD10-AS1","gene_name":"FZD10 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48632]","synonyms":"FLJ31485","biotype":"processed_transcript","ncbi_id":"440119","summary":null,"start":130144315,"end":130162256,"strand":-1,"description":"FZD10 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48632]"}, {"versioned_ensembl_gene_id":"ENSG00000275536.1","gene_symbol":"AC118459.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69826364,"end":69826946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223402.1","gene_symbol":"AC074121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98478551,"end":98479225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240828.1","gene_symbol":"AC135721.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43079302,"end":43079780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269349.1","gene_symbol":"AC022150.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52511282,"end":52512342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144355.14","gene_symbol":"DLX1","gene_name":"distal-less homeobox 1 [Source:HGNC Symbol;Acc:HGNC:2914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1745","summary":"This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein is localized to the nucleus where it may function as a transcriptional regulator of signals from multiple TGF-{beta} superfamily members. The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain. This gene is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 2. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":172084740,"end":172089677,"strand":1,"description":"distal-less homeobox 1 [Source:HGNC Symbol;Acc:HGNC:2914]"}, {"versioned_ensembl_gene_id":"ENSG00000197309.3","gene_symbol":"OR10D3","gene_name":"olfactory receptor family 10 subfamily D member 3 (putative) [Source:HGNC Symbol;Acc:HGNC:8168]","synonyms":"OR10D3P,HTPCRX09","biotype":"protein_coding","ncbi_id":"26497","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124183345,"end":124188780,"strand":1,"description":"olfactory receptor family 10 subfamily D member 3 (putative) [Source:HGNC Symbol;Acc:HGNC:8168]"}, {"versioned_ensembl_gene_id":"ENSG00000258567.1","gene_symbol":"DUX4L16","gene_name":"double homeobox 4 like 16 [Source:HGNC Symbol;Acc:HGNC:37719]","synonyms":"DUXY1","biotype":"unprocessed_pseudogene","ncbi_id":"728169","summary":null,"start":11306918,"end":11308181,"strand":1,"description":"double homeobox 4 like 16 [Source:HGNC Symbol;Acc:HGNC:37719]"}, {"versioned_ensembl_gene_id":"ENSG00000277914.1","gene_symbol":"DDX6P2","gene_name":"DEAD-box helicase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37806]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130117","summary":null,"start":86275493,"end":86277262,"strand":1,"description":"DEAD-box helicase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37806]"}, {"versioned_ensembl_gene_id":"ENSG00000278580.1","gene_symbol":"AL162373.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85837126,"end":85837532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232767.1","gene_symbol":"AC016825.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116670103,"end":116672739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256040.2","gene_symbol":"PAPPA-AS1","gene_name":"PAPPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:35152]","synonyms":"TAFII105,TAF4B,TAF2C2,PAPPAS,PAPPA-AS,NCRNA00156,DIPAS","biotype":"antisense_RNA","ncbi_id":"493913","summary":null,"start":116398157,"end":116400606,"strand":-1,"description":"PAPPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:35152]"}, {"versioned_ensembl_gene_id":"ENSG00000243715.1","gene_symbol":"CACNA2D3-AS1","gene_name":"CACNA2D3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40702]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874237","summary":null,"start":54874605,"end":54901255,"strand":-1,"description":"CACNA2D3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40702]"}, {"versioned_ensembl_gene_id":"ENSG00000265992.1","gene_symbol":"ESRG","gene_name":"embryonic stem cell related (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:39079]","synonyms":"HESRG","biotype":"sense_intronic","ncbi_id":"790952","summary":null,"start":54632122,"end":54639857,"strand":-1,"description":"embryonic stem cell related (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:39079]"}, {"versioned_ensembl_gene_id":"ENSG00000260650.1","gene_symbol":"AC010542.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66579983,"end":66580716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282252.1","gene_symbol":"AC229888.4","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142629704,"end":142630195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109065.11","gene_symbol":"NAT9","gene_name":"N-acetyltransferase 9 (putative) [Source:HGNC Symbol;Acc:HGNC:23133]","synonyms":"DKFZP564C103","biotype":"protein_coding","ncbi_id":"26151","summary":null,"start":74770547,"end":74776367,"strand":-1,"description":"N-acetyltransferase 9 (putative) [Source:HGNC Symbol;Acc:HGNC:23133]"}, {"versioned_ensembl_gene_id":"ENSG00000182752.9","gene_symbol":"PAPPA","gene_name":"pappalysin 1 [Source:HGNC Symbol;Acc:HGNC:8602]","synonyms":"DIPLA1,ASBABP2,PAPPA1,PAPP-A,PAPA,IGFBP-4ase","biotype":"protein_coding","ncbi_id":"5069","summary":"This gene encodes a secreted metalloproteinase which cleaves insulin-like growth factor binding proteins (IGFBPs). Following IGFBP cleavage, insulin growth factors dissociate from IGFBPs and bind to IGF receptors, resulting in activation of the IGF pathway. The encoded protein plays a role in bone formation, inflammation, wound healing and female fertility. Enhanced expression of this protein is associated with diabetic nephropathy in human patients and this protein may promote tumor invasion and growth in various human cancers. [provided by RefSeq, Aug 2017]","start":116153804,"end":116402322,"strand":1,"description":"pappalysin 1 [Source:HGNC Symbol;Acc:HGNC:8602]"}, {"versioned_ensembl_gene_id":"ENSG00000226604.2","gene_symbol":"PAPPA-AS2","gene_name":"PAPPA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:35160]","synonyms":"AGU1","biotype":"antisense_RNA","ncbi_id":"103611155","summary":null,"start":116285829,"end":116288769,"strand":-1,"description":"PAPPA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:35160]"}, {"versioned_ensembl_gene_id":"ENSG00000262528.2","gene_symbol":"AL022341.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":654611,"end":656194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204978.2","gene_symbol":"ERICH4","gene_name":"glutamate rich 4 [Source:HGNC Symbol;Acc:HGNC:34497]","synonyms":"LOC100170765,C19orf69","biotype":"protein_coding","ncbi_id":"100170765","summary":null,"start":41443158,"end":41444765,"strand":1,"description":"glutamate rich 4 [Source:HGNC Symbol;Acc:HGNC:34497]"}, {"versioned_ensembl_gene_id":"ENSG00000141750.6","gene_symbol":"STAC2","gene_name":"SH3 and cysteine rich domain 2 [Source:HGNC Symbol;Acc:HGNC:23990]","synonyms":"24b2","biotype":"protein_coding","ncbi_id":"342667","summary":"This gene encodes a protein containing an SH3 domain and a zinc finger domain. The encoded protein has been shown to regulate calcium channel inactivation in a human cell line. Reduced expression of this gene has been observed in human heart failure. [provided by RefSeq, May 2017]","start":39210536,"end":39225872,"strand":-1,"description":"SH3 and cysteine rich domain 2 [Source:HGNC Symbol;Acc:HGNC:23990]"}, {"versioned_ensembl_gene_id":"ENSG00000272139.1","gene_symbol":"AC113349.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122311297,"end":122311673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231825.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"G2,D6S51E,BAT2","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31611467,"end":31628517,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000284431.1","gene_symbol":"AL022238.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":40346529,"end":40410054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109062.11","gene_symbol":"SLC9A3R1","gene_name":"SLC9A3 regulator 1 [Source:HGNC Symbol;Acc:HGNC:11075]","synonyms":"NHERF1,NHERF,EBP50","biotype":"protein_coding","ncbi_id":"9368","summary":"This gene encodes a sodium/hydrogen exchanger regulatory cofactor. The protein interacts with and regulates various proteins including the cystic fibrosis transmembrane conductance regulator and G-protein coupled receptors such as the beta2-adrenergic receptor and the parathyroid hormone 1 receptor. The protein also interacts with proteins that function as linkers between integral membrane and cytoskeletal proteins. The protein localizes to actin-rich structures including membrane ruffles, microvilli, and filopodia. Mutations in this gene result in hypophosphatemic nephrolithiasis/osteoporosis type 2, and loss of heterozygosity of this gene is implicated in breast cancer.[provided by RefSeq, Sep 2009]","start":74748652,"end":74769353,"strand":1,"description":"SLC9A3 regulator 1 [Source:HGNC Symbol;Acc:HGNC:11075]"}, {"versioned_ensembl_gene_id":"ENSG00000272219.1","gene_symbol":"AC005072.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":101960116,"end":101961894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279562.1","gene_symbol":"AC090617.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2117626,"end":2117772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106701.11","gene_symbol":"FSD1L","gene_name":"fibronectin type III and SPRY domain containing 1 like [Source:HGNC Symbol;Acc:HGNC:13753]","synonyms":"FSD1NL,FSD1CL,CSDUFD1,CCDC10","biotype":"protein_coding","ncbi_id":"83856","summary":null,"start":105447796,"end":105552433,"strand":1,"description":"fibronectin type III and SPRY domain containing 1 like [Source:HGNC Symbol;Acc:HGNC:13753]"}, {"versioned_ensembl_gene_id":"ENSG00000164329.13","gene_symbol":"PAPD4","gene_name":"poly(A) RNA polymerase D4, non-canonical [Source:HGNC Symbol;Acc:HGNC:26776]","synonyms":"TUT2,GLD2,FLJ38499","biotype":"protein_coding","ncbi_id":"167153","summary":null,"start":79612120,"end":79686648,"strand":1,"description":"poly(A) RNA polymerase D4, non-canonical [Source:HGNC Symbol;Acc:HGNC:26776]"}, {"versioned_ensembl_gene_id":"ENSG00000254373.1","gene_symbol":"AC112191.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160258253,"end":160258585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282340.1","gene_symbol":"TRBV10-3","gene_name":"T-cell receptor beta variable 10-3 [Source:HGNC Symbol;Acc:HGNC:12179]","synonyms":"TRBV103,TCRBV12S1A1N2,TCRBV10S3","biotype":"TR_V_gene","ncbi_id":"28583","summary":null,"start":142586067,"end":142586516,"strand":1,"description":"T-cell receptor beta variable 10-3 [Source:HGNC Symbol;Acc:HGNC:12179]"}, {"versioned_ensembl_gene_id":"ENSG00000134056.11","gene_symbol":"MRPS36","gene_name":"mitochondrial ribosomal protein S36 [Source:HGNC Symbol;Acc:HGNC:16631]","synonyms":"MRP-S36,DC47","biotype":"protein_coding","ncbi_id":"92259","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. The mitochondrial ribosome (mitoribosome) consists of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. Pseudogenes corresponding to this gene are found on chromosomes 3p, 4q, 8p, 11q, 12q, and 20p. [provided by RefSeq, Jul 2008]","start":69217760,"end":69230129,"strand":1,"description":"mitochondrial ribosomal protein S36 [Source:HGNC Symbol;Acc:HGNC:16631]"}, {"versioned_ensembl_gene_id":"ENSG00000242728.1","gene_symbol":"UQCRHP4","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38047]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128448","summary":null,"start":70140217,"end":70140488,"strand":1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38047]"}, {"versioned_ensembl_gene_id":"ENSG00000157211.11","gene_symbol":"CDCP2","gene_name":"CUB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:27297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200008","summary":null,"start":54132968,"end":54153770,"strand":-1,"description":"CUB domain containing protein 2 [Source:HGNC Symbol;Acc:HGNC:27297]"}, {"versioned_ensembl_gene_id":"ENSG00000249271.2","gene_symbol":"HNRNPA1P44","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:48774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421432","summary":null,"start":65816302,"end":65817481,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:48774]"}, {"versioned_ensembl_gene_id":"ENSG00000104808.7","gene_symbol":"DHDH","gene_name":"dihydrodiol dehydrogenase [Source:HGNC Symbol;Acc:HGNC:17887]","synonyms":"HUM2DD","biotype":"protein_coding","ncbi_id":"27294","summary":"This gene encodes an enzyme that belongs to the family of dihydrodiol dehydrogenases, which exist in multiple forms in mammalian tissues and are involved in the metabolism of xenobiotics and sugars. These enzymes catalyze the NADP1-linked oxidation of transdihydrodiols of aromatic hydrocarbons to corresponding catechols. This enzyme is a dimeric dihydrodiol dehydrogenase, and it differs from monomeric dihydrodiol dehydrogenases in its high substrate specificity for trans-dihydrodiols of aromatic hydrocarbons in the oxidative direction. [provided by RefSeq, Jul 2008]","start":48933682,"end":48944969,"strand":1,"description":"dihydrodiol dehydrogenase [Source:HGNC Symbol;Acc:HGNC:17887]"}, {"versioned_ensembl_gene_id":"ENSG00000119698.11","gene_symbol":"PPP4R4","gene_name":"protein phosphatase 4 regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:23788]","synonyms":"PP4R4,KIAA1622,CFAP14","biotype":"protein_coding","ncbi_id":"57718","summary":"The protein encoded by this gene is a HEAT-like repeat-containing protein. The HEAT repeat is a tandemly repeated, 37-47 amino acid long module occurring in a number of cytoplasmic proteins. Arrays of HEAT repeats form a rod-like helical structure and appear to function as protein-protein interaction surfaces. The repeat-containing region of this protein has some similarity to the constant regulatory domain of the protein phosphatase 2A PR65/A subunit. The encoded protein binds protein serine/threonine phosphatase 4c in the cytoplasm. [provided by RefSeq, Jan 2017]","start":94146128,"end":94279735,"strand":1,"description":"protein phosphatase 4 regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:23788]"}, {"versioned_ensembl_gene_id":"ENSG00000266840.1","gene_symbol":"AC068254.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69704978,"end":69724975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226461.3","gene_symbol":"OR10G5P","gene_name":"olfactory receptor family 10 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14811]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79515","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124009655,"end":124010012,"strand":1,"description":"olfactory receptor family 10 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14811]"}, {"versioned_ensembl_gene_id":"ENSG00000141556.20","gene_symbol":"TBCD","gene_name":"tubulin folding cofactor D [Source:HGNC Symbol;Acc:HGNC:11581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6904","summary":"Cofactor D is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. [provided by RefSeq, Jul 2008]","start":82752064,"end":82945922,"strand":1,"description":"tubulin folding cofactor D [Source:HGNC Symbol;Acc:HGNC:11581]"}, {"versioned_ensembl_gene_id":"ENSG00000244649.4","gene_symbol":"LINC02086","gene_name":"long intergenic non-protein coding RNA 2086 [Source:HGNC Symbol;Acc:HGNC:52936]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371809","summary":null,"start":48646923,"end":48707346,"strand":1,"description":"long intergenic non-protein coding RNA 2086 [Source:HGNC Symbol;Acc:HGNC:52936]"}, {"versioned_ensembl_gene_id":"ENSG00000206052.10","gene_symbol":"DOK6","gene_name":"docking protein 6 [Source:HGNC Symbol;Acc:HGNC:28301]","synonyms":"MGC20785,HsT3226,DOK5L","biotype":"protein_coding","ncbi_id":"220164","summary":"DOK6 is a member of the DOK (see DOK1; MIM 602919) family of intracellular adaptors that play a role in the RET (MIM 164761) signaling cascade (Crowder et al., 2004 [PubMed 15286081]).[supplied by OMIM, Mar 2008]","start":69401055,"end":69849087,"strand":1,"description":"docking protein 6 [Source:HGNC Symbol;Acc:HGNC:28301]"}, {"versioned_ensembl_gene_id":"ENSG00000235443.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"RPA12,HTEX-6,tctex-6,hZR14","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30051404,"end":30057408,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000264845.2","gene_symbol":"AC119868.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":69469517,"end":69471736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197054.11","gene_symbol":"ZNF763","gene_name":"zinc finger protein 763 [Source:HGNC Symbol;Acc:HGNC:27614]","synonyms":"ZNF440L","biotype":"protein_coding","ncbi_id":"284390","summary":null,"start":11965037,"end":11980381,"strand":1,"description":"zinc finger protein 763 [Source:HGNC Symbol;Acc:HGNC:27614]"}, {"versioned_ensembl_gene_id":"ENSG00000262339.5","gene_symbol":"AC130371.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82978525,"end":82981738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242207.1","gene_symbol":"HOXB-AS4","gene_name":"HOXB cluster antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40285]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874351","summary":null,"start":48628675,"end":48634932,"strand":1,"description":"HOXB cluster antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40285]"}, {"versioned_ensembl_gene_id":"ENSG00000253256.1","gene_symbol":"AC134043.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159209921,"end":159248796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284052.1","gene_symbol":"AC006460.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":190607660,"end":190649840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101255.10","gene_symbol":"TRIB3","gene_name":"tribbles pseudokinase 3 [Source:HGNC Symbol;Acc:HGNC:16228]","synonyms":"TRB3,dJ1103G7.3,C20orf97","biotype":"protein_coding","ncbi_id":"57761","summary":"The protein encoded by this gene is a putative protein kinase that is induced by the transcription factor NF-kappaB. The encoded protein is a negative regulator of NF-kappaB and can also sensitize cells to TNF- and TRAIL-induced apoptosis. In addition, this protein can negatively regulate the cell survival serine-threonine kinase AKT1. Differential promoter usage and alternate splicing result in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":362835,"end":397559,"strand":1,"description":"tribbles pseudokinase 3 [Source:HGNC Symbol;Acc:HGNC:16228]"}, {"versioned_ensembl_gene_id":"ENSG00000235588.8","gene_symbol":"AIF1","gene_name":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]","synonyms":"IBA1,Em:AF129756.17,IRT-1,AIF-1","biotype":"protein_coding","ncbi_id":"199","summary":"This gene encodes a protein that binds actin and calcium. This gene is induced by cytokines and interferon and may promote macrophage activation and growth of vascular smooth muscle cells and T-lymphocytes. Polymorphisms in this gene may be associated with systemic sclerosis. Alternative splicing results in multiple transcript variants, but the full-length and coding nature of some of these variants is not certain. [provided by RefSeq, Jan 2016]","start":31605935,"end":31607772,"strand":1,"description":"allograft inflammatory factor 1 [Source:HGNC Symbol;Acc:HGNC:352]"}, {"versioned_ensembl_gene_id":"ENSG00000162399.6","gene_symbol":"BSND","gene_name":"barttin CLCNK type accessory beta subunit [Source:HGNC Symbol;Acc:HGNC:16512]","synonyms":"DFNB73,BART","biotype":"protein_coding","ncbi_id":"7809","summary":"This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness. [provided by RefSeq, Jul 2008]","start":54998933,"end":55010883,"strand":1,"description":"barttin CLCNK type accessory beta subunit [Source:HGNC Symbol;Acc:HGNC:16512]"}, {"versioned_ensembl_gene_id":"ENSG00000241573.1","gene_symbol":"AC011005.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129096027,"end":129096735,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171097.13","gene_symbol":"KYAT1","gene_name":"kynurenine aminotransferase 1 [Source:HGNC Symbol;Acc:HGNC:1564]","synonyms":"KATI,GTK,CCBL1","biotype":"protein_coding","ncbi_id":"883","summary":"This gene encodes a cytosolic enzyme that is responsible for the metabolism of cysteine conjugates of certain halogenated alkenes and alkanes. This metabolism can form reactive metabolites leading to nephrotoxicity and neurotoxicity. Increased levels of this enzyme have been linked to schizophrenia. Multiple transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":128832942,"end":128882494,"strand":-1,"description":"kynurenine aminotransferase 1 [Source:HGNC Symbol;Acc:HGNC:1564]"}, {"versioned_ensembl_gene_id":"ENSG00000011422.11","gene_symbol":"PLAUR","gene_name":"plasminogen activator, urokinase receptor [Source:HGNC Symbol;Acc:HGNC:9053]","synonyms":"URKR,UPAR,CD87","biotype":"protein_coding","ncbi_id":"5329","summary":"This gene encodes the receptor for urokinase plasminogen activator and, given its role in localizing and promoting plasmin formation, likely influences many normal and pathological processes related to cell-surface plasminogen activation and localized degradation of the extracellular matrix. It binds both the proprotein and mature forms of urokinase plasminogen activator and permits the activation of the receptor-bound pro-enzyme by plasmin. The protein lacks transmembrane or cytoplasmic domains and may be anchored to the plasma membrane by a glycosyl-phosphatidylinositol (GPI) moiety following cleavage of the nascent polypeptide near its carboxy-terminus. However, a soluble protein is also produced in some cell types. Alternative splicing results in multiple transcript variants encoding different isoforms. The proprotein experiences several post-translational cleavage reactions that have not yet been fully defined. [provided by RefSeq, Jul 2008]","start":43646095,"end":43670547,"strand":-1,"description":"plasminogen activator, urokinase receptor [Source:HGNC Symbol;Acc:HGNC:9053]"}, {"versioned_ensembl_gene_id":"ENSG00000241102.1","gene_symbol":"AC011005.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129095301,"end":129095811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187959.9","gene_symbol":"CPSF4L","gene_name":"cleavage and polyadenylation specific factor 4 like [Source:HGNC Symbol;Acc:HGNC:33632]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642843","summary":null,"start":73248449,"end":73262352,"strand":-1,"description":"cleavage and polyadenylation specific factor 4 like [Source:HGNC Symbol;Acc:HGNC:33632]"}, {"versioned_ensembl_gene_id":"ENSG00000277728.1","gene_symbol":"AC097641.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73202968,"end":73203431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278586.1","gene_symbol":"AC005088.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102264706,"end":102264979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233203.6","gene_symbol":"AC096536.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54887563,"end":54888850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272664.1","gene_symbol":"AC103710.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4718612,"end":4719559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223898.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425980,"end":29457549,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000226932.1","gene_symbol":"BX005432.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29269328,"end":29270287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260094.1","gene_symbol":"LINC00564","gene_name":"long intergenic non-protein coding RNA 564 [Source:HGNC Symbol;Acc:HGNC:43708]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861546","summary":null,"start":81225865,"end":81226983,"strand":-1,"description":"long intergenic non-protein coding RNA 564 [Source:HGNC Symbol;Acc:HGNC:43708]"}, {"versioned_ensembl_gene_id":"ENSG00000280309.1","gene_symbol":"AC023300.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74299503,"end":74304527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254103.1","gene_symbol":"AC009927.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58503588,"end":58504068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259618.1","gene_symbol":"AC012170.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50494018,"end":50497080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266445.1","gene_symbol":"AC124287.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82476597,"end":82477924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204963.5","gene_symbol":"PCDHA7","gene_name":"protocadherin alpha 7 [Source:HGNC Symbol;Acc:HGNC:8673]","synonyms":"CNR4,CRNR4,CNRS4","biotype":"protein_coding","ncbi_id":"56141","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140834248,"end":141012344,"strand":1,"description":"protocadherin alpha 7 [Source:HGNC Symbol;Acc:HGNC:8673]"}, {"versioned_ensembl_gene_id":"ENSG00000278946.1","gene_symbol":"AC005609.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140867513,"end":140867959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166685.11","gene_symbol":"COG1","gene_name":"component of oligomeric golgi complex 1 [Source:HGNC Symbol;Acc:HGNC:6545]","synonyms":"LDLB,KIAA1381","biotype":"protein_coding","ncbi_id":"9382","summary":"The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. It is thought that this protein is required for steps in the normal medial and trans Golgi-associated processing of glycoconjugates and plays a role in the organization of the Golgi-localized complex. [provided by RefSeq, Jul 2008]","start":73192632,"end":73208507,"strand":1,"description":"component of oligomeric golgi complex 1 [Source:HGNC Symbol;Acc:HGNC:6545]"}, {"versioned_ensembl_gene_id":"ENSG00000260298.2","gene_symbol":"ACTG1P16","gene_name":"actin gamma 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51496]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100418960","summary":null,"start":50058150,"end":50059231,"strand":-1,"description":"actin gamma 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51496]"}, {"versioned_ensembl_gene_id":"ENSG00000070814.17","gene_symbol":"TCOF1","gene_name":"treacle ribosome biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:11654]","synonyms":"TCS,treacle","biotype":"protein_coding","ncbi_id":"6949","summary":"This gene encodes a nucleolar protein with a LIS1 homology domain. The protein is involved in ribosomal DNA gene transcription through its interaction with upstream binding factor (UBF). Mutations in this gene have been associated with Treacher Collins syndrome, a disorder which includes abnormal craniofacial development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":150357639,"end":150400308,"strand":1,"description":"treacle ribosome biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:11654]"}, {"versioned_ensembl_gene_id":"ENSG00000236549.1","gene_symbol":"RPS27AP7","gene_name":"ribosomal protein S27a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35735]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728971","summary":null,"start":47883455,"end":47883909,"strand":1,"description":"ribosomal protein S27a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35735]"}, {"versioned_ensembl_gene_id":"ENSG00000275895.6","gene_symbol":"U2AF1L5","gene_name":"U2 small nuclear RNA auxiliary factor 1 like 5 [Source:HGNC Symbol;Acc:HGNC:51830]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724594","summary":null,"start":6484623,"end":6499261,"strand":-1,"description":"U2 small nuclear RNA auxiliary factor 1 like 5 [Source:HGNC Symbol;Acc:HGNC:51830]"}, {"versioned_ensembl_gene_id":"ENSG00000282126.1","gene_symbol":"AC138747.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28346477,"end":28346643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254260.1","gene_symbol":"AC015468.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20941428,"end":20950175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259843.2","gene_symbol":"AC007610.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50046429,"end":50066224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253300.1","gene_symbol":"AC018541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20655691,"end":20700134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235691.1","gene_symbol":"AC006987.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10090802,"end":10091207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224874.3","gene_symbol":"MYL8P","gene_name":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]","synonyms":"BING3","biotype":"processed_pseudogene","ncbi_id":"442204","summary":null,"start":33509323,"end":33509840,"strand":1,"description":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]"}, {"versioned_ensembl_gene_id":"ENSG00000204965.8","gene_symbol":"PCDHA5","gene_name":"protocadherin alpha 5 [Source:HGNC Symbol;Acc:HGNC:8671]","synonyms":"PCDH-ALPHA5,CRNR6,CNRS6,CNRN6,CNR6","biotype":"protein_coding","ncbi_id":"56143","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140821604,"end":141012344,"strand":1,"description":"protocadherin alpha 5 [Source:HGNC Symbol;Acc:HGNC:8671]"}, {"versioned_ensembl_gene_id":"ENSG00000234899.9","gene_symbol":"SOX9-AS1","gene_name":"SOX9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49321]","synonyms":"FLJ37644","biotype":"processed_transcript","ncbi_id":"400618","summary":null,"start":72034107,"end":72237203,"strand":-1,"description":"SOX9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49321]"}, {"versioned_ensembl_gene_id":"ENSG00000249504.3","gene_symbol":"PCDHA14","gene_name":"protocadherin alpha 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:2163]","synonyms":"CNRS3,CNR3,PCDH-PSI4,CRNR3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26307","summary":null,"start":140861224,"end":140863521,"strand":1,"description":"protocadherin alpha 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:2163]"}, {"versioned_ensembl_gene_id":"ENSG00000187017.15","gene_symbol":"ESPN","gene_name":"espin [Source:HGNC Symbol;Acc:HGNC:13281]","synonyms":"DFNB36","biotype":"protein_coding","ncbi_id":"83715","summary":"This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement. [provided by RefSeq, Nov 2009]","start":6424788,"end":6461370,"strand":1,"description":"espin [Source:HGNC Symbol;Acc:HGNC:13281]"}, {"versioned_ensembl_gene_id":"ENSG00000278478.1","gene_symbol":"AC006987.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10070131,"end":10070409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125398.5","gene_symbol":"SOX9","gene_name":"SRY-box 9 [Source:HGNC Symbol;Acc:HGNC:11204]","synonyms":"SRA1,CMPD1,CMD1","biotype":"protein_coding","ncbi_id":"6662","summary":"The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008]","start":72121020,"end":72126420,"strand":1,"description":"SRY-box 9 [Source:HGNC Symbol;Acc:HGNC:11204]"}, {"versioned_ensembl_gene_id":"ENSG00000180846.8","gene_symbol":"CSNK1G2-AS1","gene_name":"CSNK1G2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28604]","synonyms":"MGC39696,C19orf34","biotype":"antisense_RNA","ncbi_id":"255193","summary":null,"start":1952531,"end":1954586,"strand":-1,"description":"CSNK1G2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28604]"}, {"versioned_ensembl_gene_id":"ENSG00000137269.14","gene_symbol":"LRRC1","gene_name":"leucine rich repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:14307]","synonyms":"FLJ11834,FLJ10775,dJ523E19.1,LANO","biotype":"protein_coding","ncbi_id":"55227","summary":null,"start":53794497,"end":53924121,"strand":1,"description":"leucine rich repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:14307]"}, {"versioned_ensembl_gene_id":"ENSG00000204962.5","gene_symbol":"PCDHA8","gene_name":"protocadherin alpha 8 [Source:HGNC Symbol;Acc:HGNC:8674]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56140","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140841187,"end":141012344,"strand":1,"description":"protocadherin alpha 8 [Source:HGNC Symbol;Acc:HGNC:8674]"}, {"versioned_ensembl_gene_id":"ENSG00000256124.5","gene_symbol":"LINC01152","gene_name":"long intergenic non-protein coding RNA 1152 [Source:HGNC Symbol;Acc:HGNC:16752]","synonyms":"CMPD,TCONS_00025128","biotype":"lincRNA","ncbi_id":"102606463","summary":null,"start":72030291,"end":72041297,"strand":1,"description":"long intergenic non-protein coding RNA 1152 [Source:HGNC Symbol;Acc:HGNC:16752]"}, {"versioned_ensembl_gene_id":"ENSG00000248400.2","gene_symbol":"ST13P12","gene_name":"ST13, Hsp70 interacting protein pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38787]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127911","summary":null,"start":82968888,"end":82977153,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38787]"}, {"versioned_ensembl_gene_id":"ENSG00000267471.1","gene_symbol":"AC005771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70628917,"end":70629265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267170.1","gene_symbol":"AC005242.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70241324,"end":70241761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279028.1","gene_symbol":"AC010223.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140966212,"end":140966490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123700.4","gene_symbol":"KCNJ2","gene_name":"potassium voltage-gated channel subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:6263]","synonyms":"LQT7,Kir2.1,IRK1","biotype":"protein_coding","ncbi_id":"3759","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]","start":70168673,"end":70180048,"strand":1,"description":"potassium voltage-gated channel subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:6263]"}, {"versioned_ensembl_gene_id":"ENSG00000169660.15","gene_symbol":"HEXDC","gene_name":"hexosaminidase D [Source:HGNC Symbol;Acc:HGNC:26307]","synonyms":"FLJ23825","biotype":"protein_coding","ncbi_id":"284004","summary":null,"start":82418318,"end":82442645,"strand":1,"description":"hexosaminidase D [Source:HGNC Symbol;Acc:HGNC:26307]"}, {"versioned_ensembl_gene_id":"ENSG00000279066.1","gene_symbol":"AC132938.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":82425498,"end":82427310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278537.1","gene_symbol":"IGKV2OR2-8","gene_name":"immunoglobulin kappa variable 2/OR2-8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5811]","synonyms":"IGKV2/OR2-8","biotype":"IG_V_pseudogene","ncbi_id":"100996600","summary":null,"start":97376674,"end":97376973,"strand":1,"description":"immunoglobulin kappa variable 2/OR2-8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5811]"}, {"versioned_ensembl_gene_id":"ENSG00000264812.1","gene_symbol":"AC132938.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":82400703,"end":82401382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125551.18","gene_symbol":"PLGLB2","gene_name":"plasminogen-like B2 [Source:HGNC Symbol;Acc:HGNC:9073]","synonyms":"PLGP1","biotype":"protein_coding","ncbi_id":"5342","summary":null,"start":87748087,"end":87758793,"strand":1,"description":"plasminogen-like B2 [Source:HGNC Symbol;Acc:HGNC:9073]"}, {"versioned_ensembl_gene_id":"ENSG00000278576.1","gene_symbol":"AL162171.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":88589231,"end":88592408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274443.4","gene_symbol":"C8orf89","gene_name":"chromosome 8 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:51258]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130301","summary":null,"start":73241329,"end":73259502,"strand":-1,"description":"chromosome 8 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:51258]"}, {"versioned_ensembl_gene_id":"ENSG00000282317.1","gene_symbol":"AL451007.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":244731024,"end":244731586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233831.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28995715,"end":29006139,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000215114.8","gene_symbol":"UBXN2B","gene_name":"UBX domain protein 2B [Source:HGNC Symbol;Acc:HGNC:27035]","synonyms":"p37","biotype":"protein_coding","ncbi_id":"137886","summary":null,"start":58411264,"end":58451501,"strand":1,"description":"UBX domain protein 2B [Source:HGNC Symbol;Acc:HGNC:27035]"}, {"versioned_ensembl_gene_id":"ENSG00000103245.13","gene_symbol":"NARFL","gene_name":"nuclear prelamin A recognition factor like [Source:HGNC Symbol;Acc:HGNC:14179]","synonyms":"PRN,NAR1,IOP1,HPRN,FLJ21988","biotype":"protein_coding","ncbi_id":"64428","summary":null,"start":729753,"end":741329,"strand":-1,"description":"nuclear prelamin A recognition factor like [Source:HGNC Symbol;Acc:HGNC:14179]"}, {"versioned_ensembl_gene_id":"ENSG00000282098.1","gene_symbol":"TRBV5-6","gene_name":"T-cell receptor beta variable 5-6 [Source:HGNC Symbol;Acc:HGNC:12223]","synonyms":"TRBV56,TCRBV5S6,TCRBV5S2","biotype":"TR_V_gene","ncbi_id":"28609","summary":null,"start":142521745,"end":142522251,"strand":1,"description":"T-cell receptor beta variable 5-6 [Source:HGNC Symbol;Acc:HGNC:12223]"}, {"versioned_ensembl_gene_id":"ENSG00000279806.1","gene_symbol":"AC018629.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40473554,"end":40475289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125841.12","gene_symbol":"NRSN2","gene_name":"neurensin 2 [Source:HGNC Symbol;Acc:HGNC:16229]","synonyms":"dJ1103G7.6,C20orf98","biotype":"protein_coding","ncbi_id":"80023","summary":null,"start":346782,"end":359660,"strand":1,"description":"neurensin 2 [Source:HGNC Symbol;Acc:HGNC:16229]"}, {"versioned_ensembl_gene_id":"ENSG00000228902.1","gene_symbol":"ST6GALNAC2P1","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45160]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422716","summary":null,"start":84039885,"end":84040720,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45160]"}, {"versioned_ensembl_gene_id":"ENSG00000227307.1","gene_symbol":"AC010998.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120925547,"end":120980700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273232.1","gene_symbol":"AC090912.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22882825,"end":22883357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283886.1","gene_symbol":"BX664615.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":39816599,"end":39874562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237846.1","gene_symbol":"AL773545.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40105822,"end":40106527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198416.9","gene_symbol":"ZNF658B","gene_name":"zinc finger protein 658B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:32033]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401509","summary":null,"start":39443815,"end":39508885,"strand":-1,"description":"zinc finger protein 658B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:32033]"}, {"versioned_ensembl_gene_id":"ENSG00000196476.11","gene_symbol":"C20orf96","gene_name":"chromosome 20 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:16227]","synonyms":"dJ1103G7.2","biotype":"protein_coding","ncbi_id":"140680","summary":null,"start":270863,"end":290778,"strand":-1,"description":"chromosome 20 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:16227]"}, {"versioned_ensembl_gene_id":"ENSG00000214776.11","gene_symbol":"AC092821.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":9467552,"end":9576275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264050.1","gene_symbol":"AC005412.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29197071,"end":29197785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129562.10","gene_symbol":"DAD1","gene_name":"defender against cell death 1 [Source:HGNC Symbol;Acc:HGNC:2664]","synonyms":"OST2","biotype":"protein_coding","ncbi_id":"1603","summary":"DAD1, the defender against apoptotic cell death, was initially identified as a negative regulator of programmed cell death in the temperature sensitive tsBN7 cell line. The DAD1 protein disappeared in temperature-sensitive cells following a shift to the nonpermissive temperature, suggesting that loss of the DAD1 protein triggered apoptosis. DAD1 is believed to be a tightly associated subunit of oligosaccharyltransferase both in the intact membrane and in the purified enzyme, thus reflecting the essential nature of N-linked glycosylation in eukaryotes. [provided by RefSeq, Jul 2008]","start":22564905,"end":22589269,"strand":-1,"description":"defender against cell death 1 [Source:HGNC Symbol;Acc:HGNC:2664]"}, {"versioned_ensembl_gene_id":"ENSG00000259001.3","gene_symbol":"AL355075.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20343048,"end":20343685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139629.15","gene_symbol":"GALNT6","gene_name":"polypeptide N-acetylgalactosaminyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:4128]","synonyms":"GalNAc-T6","biotype":"protein_coding","ncbi_id":"11226","summary":"This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. The encoded protein is capable of glycosylating fibronectin peptide in vitro and is expressed in a fibroblast cell line, indicating that it may be involved in the synthesis of oncofetal fibronectin. [provided by RefSeq, Jul 2008]","start":51351247,"end":51392867,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:4128]"}, {"versioned_ensembl_gene_id":"ENSG00000227676.3","gene_symbol":"LINC01068","gene_name":"long intergenic non-protein coding RNA 1068 [Source:HGNC Symbol;Acc:HGNC:49106]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103724388","summary":null,"start":79566727,"end":79571436,"strand":1,"description":"long intergenic non-protein coding RNA 1068 [Source:HGNC Symbol;Acc:HGNC:49106]"}, {"versioned_ensembl_gene_id":"ENSG00000214826.5","gene_symbol":"DDX12P","gene_name":"DEAD/H-box helicase 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:2737]","synonyms":"DDX12,CHLR2","biotype":"unprocessed_pseudogene","ncbi_id":"440081","summary":null,"start":9418673,"end":9448229,"strand":-1,"description":"DEAD/H-box helicase 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:2737]"}, {"versioned_ensembl_gene_id":"ENSG00000056736.9","gene_symbol":"IL17RB","gene_name":"interleukin 17 receptor B [Source:HGNC Symbol;Acc:HGNC:18015]","synonyms":"IL17RH1,IL17BR,EVI27,CRL4","biotype":"protein_coding","ncbi_id":"55540","summary":"The protein encoded by this gene is a cytokine receptor. This receptor specifically binds to IL17B and IL17E, but does not bind to IL17 and IL17C. This receptor has been shown to mediate the activation of NF-kappaB and the production of IL8 induced by IL17E. The expression of the rat counterpart of this gene was found to be significantly up-regulated during intestinal inflammation, which suggested the immunoregulatory activity of this receptor. [provided by RefSeq, Jul 2008]","start":53846580,"end":53865800,"strand":1,"description":"interleukin 17 receptor B [Source:HGNC Symbol;Acc:HGNC:18015]"}, {"versioned_ensembl_gene_id":"ENSG00000242321.1","gene_symbol":"RPL23AP40","gene_name":"ribosomal protein L23a pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:35587]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271462","summary":null,"start":138796851,"end":138797240,"strand":1,"description":"ribosomal protein L23a pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:35587]"}, {"versioned_ensembl_gene_id":"ENSG00000112499.12","gene_symbol":"SLC22A2","gene_name":"solute carrier family 22 member 2 [Source:HGNC Symbol;Acc:HGNC:10966]","synonyms":"OCT2","biotype":"protein_coding","ncbi_id":"6582","summary":"Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. It is found primarily in the kidney, where it may mediate the first step in cation reabsorption. [provided by RefSeq, Jul 2008]","start":160171061,"end":160277638,"strand":-1,"description":"solute carrier family 22 member 2 [Source:HGNC Symbol;Acc:HGNC:10966]"}, {"versioned_ensembl_gene_id":"ENSG00000213793.5","gene_symbol":"ZNF888","gene_name":"zinc finger protein 888 [Source:HGNC Symbol;Acc:HGNC:38695]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388559","summary":null,"start":52904417,"end":52923481,"strand":-1,"description":"zinc finger protein 888 [Source:HGNC Symbol;Acc:HGNC:38695]"}, {"versioned_ensembl_gene_id":"ENSG00000258360.1","gene_symbol":"NF1P12","gene_name":"neurofibromin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51739]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418983","summary":null,"start":38206231,"end":38207192,"strand":-1,"description":"neurofibromin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51739]"}, {"versioned_ensembl_gene_id":"ENSG00000269583.1","gene_symbol":"L34079.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43574638,"end":43575618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284306.1","gene_symbol":"AC018793.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4242056,"end":4242640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256947.1","gene_symbol":"AP002518.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114210616,"end":114356571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223373.1","gene_symbol":"AC108066.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212911003,"end":212919809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277077.1","gene_symbol":"AL158032.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21287634,"end":21287828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235519.2","gene_symbol":"LINC01815","gene_name":"long intergenic non-protein coding RNA 1815 [Source:HGNC Symbol;Acc:HGNC:52619]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507201","summary":null,"start":81461358,"end":81467468,"strand":-1,"description":"long intergenic non-protein coding RNA 1815 [Source:HGNC Symbol;Acc:HGNC:52619]"}, {"versioned_ensembl_gene_id":"ENSG00000102763.17","gene_symbol":"VWA8","gene_name":"von Willebrand factor A domain containing 8 [Source:HGNC Symbol;Acc:HGNC:29071]","synonyms":"KIAA0564","biotype":"protein_coding","ncbi_id":"23078","summary":null,"start":41566837,"end":41961120,"strand":-1,"description":"von Willebrand factor A domain containing 8 [Source:HGNC Symbol;Acc:HGNC:29071]"}, {"versioned_ensembl_gene_id":"ENSG00000159189.11","gene_symbol":"C1QC","gene_name":"complement C1q C chain [Source:HGNC Symbol;Acc:HGNC:1245]","synonyms":"C1QG","biotype":"protein_coding","ncbi_id":"714","summary":"This gene encodes the C-chain polypeptide of serum complement subcomponent C1q, which associates with C1r and C1s to yield the first component of the serum complement system. C1q is composed of 18 polypeptide chains which include 6 A-chains, 6 B-chains, and 6 C-chains. Each chain contains an N-terminal collagen-like region and a C-terminal C1q globular domain. C1q deficiency is associated with lupus erythematosus and glomerulonephritis. [provided by RefSeq, Dec 2016]","start":22643630,"end":22648110,"strand":1,"description":"complement C1q C chain [Source:HGNC Symbol;Acc:HGNC:1245]"}, {"versioned_ensembl_gene_id":"ENSG00000132563.15","gene_symbol":"REEP2","gene_name":"receptor accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:17975]","synonyms":"Yip2d,SPG72,SGC32445,C5orf19","biotype":"protein_coding","ncbi_id":"51308","summary":"This gene encodes a member of the receptor expression enhancing protein family. Studies of a related gene in mouse suggest that the encoded protein is found in the cell membrane and enhances the function of sweet taste receptors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":138439017,"end":138446969,"strand":1,"description":"receptor accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:17975]"}, {"versioned_ensembl_gene_id":"ENSG00000273523.1","gene_symbol":"AL139082.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52128891,"end":52132723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264236.1","gene_symbol":"AC096708.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68992718,"end":68993375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272986.1","gene_symbol":"AC009570.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70703747,"end":70704491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256070.1","gene_symbol":"AC016956.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33454345,"end":33455452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278740.1","gene_symbol":"AC005332.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68188547,"end":68189165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278730.1","gene_symbol":"AC005332.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68126666,"end":68129586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222041.10","gene_symbol":"CYTOR","gene_name":"cytoskeleton regulator RNA [Source:HGNC Symbol;Acc:HGNC:28717]","synonyms":"NCRNA00152,MGC4677,LINC00152,C2orf59","biotype":"lincRNA","ncbi_id":"112597","summary":"This gene produces a long non-coding RNA that is overexpressed in cancer cells and promotes cell proliferation and epithelial-mesenchymal transition. This RNA may bind enhancer of zeste homolog 2 and participate in the transcriptional silencing of tumor suppressor genes. It may act as a sponge for microRNAs. Alternatively spliced variants have been observed. [provided by RefSeq, Dec 2017]","start":87455368,"end":87606805,"strand":1,"description":"cytoskeleton regulator RNA [Source:HGNC Symbol;Acc:HGNC:28717]"}, {"versioned_ensembl_gene_id":"ENSG00000125746.16","gene_symbol":"EML2","gene_name":"echinoderm microtubule associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:18035]","synonyms":"EMAP2,EMAP-2,ELP70","biotype":"protein_coding","ncbi_id":"24139","summary":null,"start":45606994,"end":45645629,"strand":-1,"description":"echinoderm microtubule associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:18035]"}, {"versioned_ensembl_gene_id":"ENSG00000266598.1","gene_symbol":"AC037487.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65051909,"end":65053308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251620.1","gene_symbol":"STPG2-AS1","gene_name":"STPG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41209]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410545","summary":null,"start":97366926,"end":97490164,"strand":1,"description":"STPG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41209]"}, {"versioned_ensembl_gene_id":"ENSG00000231585.1","gene_symbol":"AC034228.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132011448,"end":132013199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250893.1","gene_symbol":"AC098869.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40426119,"end":40427585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197170.9","gene_symbol":"PSMD12","gene_name":"proteasome 26S subunit, non-ATPase 12 [Source:HGNC Symbol;Acc:HGNC:9557]","synonyms":"p55,Rpn5","biotype":"protein_coding","ncbi_id":"5718","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. A pseudogene has been identified on chromosome 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":67337916,"end":67366627,"strand":-1,"description":"proteasome 26S subunit, non-ATPase 12 [Source:HGNC Symbol;Acc:HGNC:9557]"}, {"versioned_ensembl_gene_id":"ENSG00000229972.7","gene_symbol":"IQCF3","gene_name":"IQ motif containing F3 [Source:HGNC Symbol;Acc:HGNC:31816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401067","summary":null,"start":51817604,"end":51830856,"strand":1,"description":"IQ motif containing F3 [Source:HGNC Symbol;Acc:HGNC:31816]"}, {"versioned_ensembl_gene_id":"ENSG00000112303.13","gene_symbol":"VNN2","gene_name":"vanin 2 [Source:HGNC Symbol;Acc:HGNC:12706]","synonyms":"GPI-80,FOAP-4","biotype":"protein_coding","ncbi_id":"8875","summary":"This gene product is a member of the Vanin family of proteins that share extensive sequence similarity with each other, and also with biotinidase. The family includes secreted and membrane-associated proteins, a few of which have been reported to participate in hematopoietic cell trafficking. No biotinidase activity has been demonstrated for any of the vanin proteins, however, they possess pantetheinase activity, which may play a role in oxidative-stress response. The encoded protein is a GPI-anchored cell surface molecule that plays a role in transendothelial migration of neutrophils. This gene lies in close proximity to, and in same transcriptional orientation as two other vanin genes on chromosome 6q23-q24. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]","start":132743870,"end":132763459,"strand":-1,"description":"vanin 2 [Source:HGNC Symbol;Acc:HGNC:12706]"}, {"versioned_ensembl_gene_id":"ENSG00000048392.11","gene_symbol":"RRM2B","gene_name":"ribonucleotide reductase regulatory TP53 inducible subunit M2B [Source:HGNC Symbol;Acc:HGNC:17296]","synonyms":"p53R2","biotype":"protein_coding","ncbi_id":"50484","summary":"This gene encodes the small subunit of a p53-inducible ribonucleotide reductase. This heterotetrameric enzyme catalyzes the conversion of ribonucleoside diphosphates to deoxyribonucleoside diphosphates. The product of this reaction is necessary for DNA synthesis. Mutations in this gene have been associated with autosomal recessive mitochondrial DNA depletion syndrome, autosomal dominant progressive external ophthalmoplegia-5, and mitochondrial neurogastrointestinal encephalopathy. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]","start":102204502,"end":102239118,"strand":-1,"description":"ribonucleotide reductase regulatory TP53 inducible subunit M2B [Source:HGNC Symbol;Acc:HGNC:17296]"}, {"versioned_ensembl_gene_id":"ENSG00000182809.10","gene_symbol":"CRIP2","gene_name":"cysteine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:2361]","synonyms":"ESP1,CRP2","biotype":"protein_coding","ncbi_id":"1397","summary":"This gene encodes a putative transcription factor with two LIM zinc-binding domains. The encoded protein may participate in the differentiation of smooth muscle tissue. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":105472962,"end":105480170,"strand":1,"description":"cysteine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:2361]"}, {"versioned_ensembl_gene_id":"ENSG00000173389.15","gene_symbol":"IQCF1","gene_name":"IQ motif containing F1 [Source:HGNC Symbol;Acc:HGNC:28607]","synonyms":"MGC39725","biotype":"protein_coding","ncbi_id":"132141","summary":null,"start":51894876,"end":51903335,"strand":-1,"description":"IQ motif containing F1 [Source:HGNC Symbol;Acc:HGNC:28607]"}, {"versioned_ensembl_gene_id":"ENSG00000064419.13","gene_symbol":"TNPO3","gene_name":"transportin 3 [Source:HGNC Symbol;Acc:HGNC:17103]","synonyms":"TRN-SR2,TRN-SR,MTR10A,LGMD1F,IPO12","biotype":"protein_coding","ncbi_id":"23534","summary":"The protein encoded by this gene is a nuclear import receptor for serine/arginine-rich (SR) proteins such as the splicing factors SFRS1 and SFRS2. The encoded protein has also been shown to be involved in HIV-1 infection, apparently through interaction with the HIV-1 capsid protein. Several protein-coding and non-coding transcript variants have been found for this gene. [provided by RefSeq, Apr 2020]","start":128954180,"end":129055173,"strand":-1,"description":"transportin 3 [Source:HGNC Symbol;Acc:HGNC:17103]"}, {"versioned_ensembl_gene_id":"ENSG00000251023.1","gene_symbol":"AC114980.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93860669,"end":93863825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185024.16","gene_symbol":"BRF1","gene_name":"BRF1, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:11551]","synonyms":"TFIIIB90,TAF3C,TAF3B2,hBRF,GTF3B,BRF","biotype":"protein_coding","ncbi_id":"2972","summary":"This gene encodes one of the three subunits of the RNA polymerase III transcription factor complex. This complex plays a central role in transcription initiation by RNA polymerase III on genes encoding tRNA, 5S rRNA, and other small structural RNAs. The gene product belongs to the TF2B family. Several alternatively spliced variants encoding different isoforms, that function at different promoters transcribed by RNA polymerase III, have been identified. [provided by RefSeq, Jun 2011]","start":105209286,"end":105315589,"strand":-1,"description":"BRF1, RNA polymerase III transcription initiation factor subunit [Source:HGNC Symbol;Acc:HGNC:11551]"}, {"versioned_ensembl_gene_id":"ENSG00000165383.11","gene_symbol":"LRRC18","gene_name":"leucine rich repeat containing 18 [Source:HGNC Symbol;Acc:HGNC:23199]","synonyms":"VKGE9338,UNQ9338,UNQ933,MGC34773","biotype":"protein_coding","ncbi_id":"474354","summary":null,"start":48909483,"end":48914232,"strand":-1,"description":"leucine rich repeat containing 18 [Source:HGNC Symbol;Acc:HGNC:23199]"}, {"versioned_ensembl_gene_id":"ENSG00000112592.13","gene_symbol":"TBP","gene_name":"TATA-box binding protein [Source:HGNC Symbol;Acc:HGNC:11588]","synonyms":"TFIID,SCA17,GTF2D1","biotype":"protein_coding","ncbi_id":"6908","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes TBP, the TATA-binding protein. A distinctive feature of TBP is a long string of glutamines in the N-terminus. This region of the protein modulates the DNA binding activity of the C terminus, and modulation of DNA binding affects the rate of transcription complex formation and initiation of transcription. The number of CAG repeats encoding the polyglutamine tract is usually 25-42, and expansion of the number of repeats to 45-66 increases the length of the polyglutamine string and is associated with spinocerebellar ataxia 17, a neurodegenerative disorder classified as a polyglutamine disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016]","start":170554302,"end":170572870,"strand":1,"description":"TATA-box binding protein [Source:HGNC Symbol;Acc:HGNC:11588]"}, {"versioned_ensembl_gene_id":"ENSG00000157335.20","gene_symbol":"CLEC18C","gene_name":"C-type lectin domain family 18 member C [Source:HGNC Symbol;Acc:HGNC:28538]","synonyms":"MRCL3,MGC34761","biotype":"protein_coding","ncbi_id":"283971","summary":null,"start":70173322,"end":70187361,"strand":1,"description":"C-type lectin domain family 18 member C [Source:HGNC Symbol;Acc:HGNC:28538]"}, {"versioned_ensembl_gene_id":"ENSG00000232032.1","gene_symbol":"AC079781.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97908256,"end":97908424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257025.1","gene_symbol":"AC023595.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":128399978,"end":128404814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143622.10","gene_symbol":"RIT1","gene_name":"Ras like without CAAX 1 [Source:HGNC Symbol;Acc:HGNC:10023]","synonyms":"ROC1,RIT,RIBB,MGC125865,MGC125864","biotype":"protein_coding","ncbi_id":"6016","summary":"This gene encodes a member of a subfamily of Ras-related GTPases. The encoded protein is involved in regulating p38 MAPK-dependent signaling cascades related to cellular stress. This protein also cooperates with nerve growth factor to promote neuronal development and regeneration. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":155897808,"end":155911404,"strand":-1,"description":"Ras like without CAAX 1 [Source:HGNC Symbol;Acc:HGNC:10023]"}, {"versioned_ensembl_gene_id":"ENSG00000170858.10","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000235672.1","gene_symbol":"AC090286.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18908279,"end":18908865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233859.2","gene_symbol":"ADH5P4","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21377]","synonyms":"bA707M13.2,ADH5B","biotype":"processed_pseudogene","ncbi_id":"642443","summary":null,"start":65836930,"end":65838039,"strand":-1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21377]"}, {"versioned_ensembl_gene_id":"ENSG00000255285.1","gene_symbol":"AP004833.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89789412,"end":89789733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231957.2","gene_symbol":"GNAI2P2","gene_name":"G protein subunit alpha i2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45110]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401646","summary":null,"start":78068623,"end":78069538,"strand":-1,"description":"G protein subunit alpha i2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45110]"}, {"versioned_ensembl_gene_id":"ENSG00000211871.1","gene_symbol":"TRAJ18","gene_name":"T-cell receptor alpha joining 18 [Source:HGNC Symbol;Acc:HGNC:12046]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28737","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22525650,"end":22525715,"strand":1,"description":"T-cell receptor alpha joining 18 [Source:HGNC Symbol;Acc:HGNC:12046]"}, {"versioned_ensembl_gene_id":"ENSG00000211870.1","gene_symbol":"TRAJ19","gene_name":"T-cell receptor alpha joining 19 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12047]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28736","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22525263,"end":22525322,"strand":1,"description":"T-cell receptor alpha joining 19 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12047]"}, {"versioned_ensembl_gene_id":"ENSG00000229562.1","gene_symbol":"ZFYVE9P1","gene_name":"zinc finger FYVE-type containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289259","summary":null,"start":137660519,"end":137662242,"strand":1,"description":"zinc finger FYVE-type containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33359]"}, {"versioned_ensembl_gene_id":"ENSG00000230681.1","gene_symbol":"CEACAMP4","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1826]","synonyms":"CGM11","biotype":"unprocessed_pseudogene","ncbi_id":"1093","summary":null,"start":43303171,"end":43304523,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1826]"}, {"versioned_ensembl_gene_id":"ENSG00000214121.4","gene_symbol":"PRDX1P1","gene_name":"peroxiredoxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11711]","synonyms":"TDPX2,PAGB","biotype":"processed_pseudogene","ncbi_id":"7002","summary":null,"start":12972843,"end":12973438,"strand":-1,"description":"peroxiredoxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11711]"}, {"versioned_ensembl_gene_id":"ENSG00000213690.3","gene_symbol":"AL360271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242376923,"end":242377432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235467.1","gene_symbol":"RPL10AP5","gene_name":"ribosomal protein L10a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645998","summary":null,"start":242365189,"end":242365822,"strand":1,"description":"ribosomal protein L10a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36770]"}, {"versioned_ensembl_gene_id":"ENSG00000054282.15","gene_symbol":"SDCCAG8","gene_name":"serologically defined colon cancer antigen 8 [Source:HGNC Symbol;Acc:HGNC:10671]","synonyms":"SLSN7,NY-CO-8,NPHP10,CCCAP,BBS16","biotype":"protein_coding","ncbi_id":"10806","summary":"This gene encodes a centrosome associated protein. This protein may be involved in organizing the centrosome during interphase and mitosis. Mutations in this gene are associated with retinal-renal ciliopathy. [provided by RefSeq, Oct 2010]","start":243256034,"end":243500092,"strand":1,"description":"serologically defined colon cancer antigen 8 [Source:HGNC Symbol;Acc:HGNC:10671]"}, {"versioned_ensembl_gene_id":"ENSG00000233508.2","gene_symbol":"AL021395.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43190101,"end":43202599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007312.12","gene_symbol":"CD79B","gene_name":"CD79b molecule [Source:HGNC Symbol;Acc:HGNC:1699]","synonyms":"B29,IGB","biotype":"protein_coding","ncbi_id":"974","summary":"The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-beta protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":63928740,"end":63932354,"strand":-1,"description":"CD79b molecule [Source:HGNC Symbol;Acc:HGNC:1699]"}, {"versioned_ensembl_gene_id":"ENSG00000182950.2","gene_symbol":"ODF3L1","gene_name":"outer dense fiber of sperm tails 3 like 1 [Source:HGNC Symbol;Acc:HGNC:28735]","synonyms":"MGC48986","biotype":"protein_coding","ncbi_id":"161753","summary":null,"start":75723977,"end":75727688,"strand":1,"description":"outer dense fiber of sperm tails 3 like 1 [Source:HGNC Symbol;Acc:HGNC:28735]"}, {"versioned_ensembl_gene_id":"ENSG00000211869.1","gene_symbol":"TRAJ20","gene_name":"T-cell receptor alpha joining 20 [Source:HGNC Symbol;Acc:HGNC:12049]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28735","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22524325,"end":22524381,"strand":1,"description":"T-cell receptor alpha joining 20 [Source:HGNC Symbol;Acc:HGNC:12049]"}, {"versioned_ensembl_gene_id":"ENSG00000227317.6","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31709206,"end":31712785,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000273100.1","gene_symbol":"AL596442.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170178681,"end":170179660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280120.1","gene_symbol":"AC073857.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123152324,"end":123153377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243818.4","gene_symbol":"AC021074.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142926675,"end":142942534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223550.1","gene_symbol":"SNRPBP1","gene_name":"small nuclear ribonucleoprotein polypeptides B and B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38665]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499258","summary":null,"start":80377554,"end":80377835,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptides B and B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38665]"}, {"versioned_ensembl_gene_id":"ENSG00000248696.1","gene_symbol":"AC011406.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150014785,"end":150015154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155850.7","gene_symbol":"SLC26A2","gene_name":"solute carrier family 26 member 2 [Source:HGNC Symbol;Acc:HGNC:10994]","synonyms":"DTDST,DTD","biotype":"protein_coding","ncbi_id":"1836","summary":"The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization. [provided by RefSeq, Jul 2008]","start":149960737,"end":149993455,"strand":1,"description":"solute carrier family 26 member 2 [Source:HGNC Symbol;Acc:HGNC:10994]"}, {"versioned_ensembl_gene_id":"ENSG00000250289.1","gene_symbol":"VWA8P1","gene_name":"von Willebrand factor A domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44271]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480787","summary":null,"start":68854910,"end":68855085,"strand":-1,"description":"von Willebrand factor A domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44271]"}, {"versioned_ensembl_gene_id":"ENSG00000171475.13","gene_symbol":"WIPF2","gene_name":"WAS/WASL interacting protein family member 2 [Source:HGNC Symbol;Acc:HGNC:30923]","synonyms":"WIRE,WICH","biotype":"protein_coding","ncbi_id":"147179","summary":"This gene encodes a WASP interacting protein (WIP)-related protein. It has been shown that this protein has a role in the WASP-mediated organization of the actin cytoskeleton and that this protein is a potential link between the activated platelet-derived growth factor receptor and the actin polymerization machinery. [provided by RefSeq, Jul 2008]","start":40219304,"end":40284136,"strand":1,"description":"WAS/WASL interacting protein family member 2 [Source:HGNC Symbol;Acc:HGNC:30923]"}, {"versioned_ensembl_gene_id":"ENSG00000118655.4","gene_symbol":"DCLRE1B","gene_name":"DNA cross-link repair 1B [Source:HGNC Symbol;Acc:HGNC:17641]","synonyms":"SNM1B,FLJ13998,FLJ12810","biotype":"protein_coding","ncbi_id":"64858","summary":"DNA interstrand cross-links prevent strand separation, thereby physically blocking transcription, replication, and segregation of DNA. DCLRE1B is one of several evolutionarily conserved genes involved in repair of interstrand cross-links (Dronkert et al., 2000 [PubMed 10848582]).[supplied by OMIM, Mar 2008]","start":113905141,"end":113914086,"strand":1,"description":"DNA cross-link repair 1B [Source:HGNC Symbol;Acc:HGNC:17641]"}, {"versioned_ensembl_gene_id":"ENSG00000275716.1","gene_symbol":"AL080285.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100093311,"end":100093768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259077.1","gene_symbol":"AL136501.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87810982,"end":87838339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052841.14","gene_symbol":"TTC17","gene_name":"tetratricopeptide repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:25596]","synonyms":"FLJ10890","biotype":"protein_coding","ncbi_id":"55761","summary":null,"start":43358932,"end":43494933,"strand":1,"description":"tetratricopeptide repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:25596]"}, {"versioned_ensembl_gene_id":"ENSG00000167325.14","gene_symbol":"RRM1","gene_name":"ribonucleotide reductase catalytic subunit M1 [Source:HGNC Symbol;Acc:HGNC:10451]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6240","summary":"This gene encodes the large and catalytic subunit of ribonucleotide reductase, an enzyme essential for the conversion of ribonucleotides into deoxyribonucleotides. A pool of available deoxyribonucleotides is important for DNA replication during S phase of the cell cycle as well as multiple DNA repair processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":4094707,"end":4138876,"strand":1,"description":"ribonucleotide reductase catalytic subunit M1 [Source:HGNC Symbol;Acc:HGNC:10451]"}, {"versioned_ensembl_gene_id":"ENSG00000258966.1","gene_symbol":"GTF3AP2","gene_name":"general transcription factor IIIA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49745]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106480682","summary":null,"start":71044375,"end":71044640,"strand":-1,"description":"general transcription factor IIIA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49745]"}, {"versioned_ensembl_gene_id":"ENSG00000206286.11","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"ARE1,SACM2L","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33179079,"end":33200871,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000226534.1","gene_symbol":"AP000552.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21370064,"end":21371945,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237050.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30100364,"end":30109841,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000136478.7","gene_symbol":"TEX2","gene_name":"testis expressed 2 [Source:HGNC Symbol;Acc:HGNC:30884]","synonyms":"TMEM96,KIAA1738,HT008","biotype":"protein_coding","ncbi_id":"55852","summary":null,"start":64147227,"end":64263301,"strand":-1,"description":"testis expressed 2 [Source:HGNC Symbol;Acc:HGNC:30884]"}, {"versioned_ensembl_gene_id":"ENSG00000243609.1","gene_symbol":"AC026470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48577524,"end":48578369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211844.1","gene_symbol":"TRAJ45","gene_name":"T-cell receptor alpha joining 45 [Source:HGNC Symbol;Acc:HGNC:12076]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28710","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22493925,"end":22493990,"strand":1,"description":"T-cell receptor alpha joining 45 [Source:HGNC Symbol;Acc:HGNC:12076]"}, {"versioned_ensembl_gene_id":"ENSG00000230589.1","gene_symbol":"IMP3P1","gene_name":"IMP3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49385]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646087","summary":null,"start":10829752,"end":10830308,"strand":-1,"description":"IMP3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49385]"}, {"versioned_ensembl_gene_id":"ENSG00000272545.1","gene_symbol":"AC023813.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48640473,"end":48641052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126012.11","gene_symbol":"KDM5C","gene_name":"lysine demethylase 5C [Source:HGNC Symbol;Acc:HGNC:11114]","synonyms":"XE169,SMCX,MRX13,JARID1C,DXS1272E","biotype":"protein_coding","ncbi_id":"8242","summary":"This gene is a member of the SMCY homolog family and encodes a protein with one ARID domain, one JmjC domain, one JmjN domain and two PHD-type zinc fingers. The DNA-binding motifs suggest this protein is involved in the regulation of transcription and chromatin remodeling. Mutations in this gene have been associated with X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":53191321,"end":53225422,"strand":-1,"description":"lysine demethylase 5C [Source:HGNC Symbol;Acc:HGNC:11114]"}, {"versioned_ensembl_gene_id":"ENSG00000278720.1","gene_symbol":"AL669942.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66042646,"end":66043342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226668.5","gene_symbol":"AL136981.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92882567,"end":92899608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257021.1","gene_symbol":"HSPE1P20","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288726","summary":null,"start":126912034,"end":126912322,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49339]"}, {"versioned_ensembl_gene_id":"ENSG00000279688.1","gene_symbol":"AQP7P3","gene_name":"aquaporin 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31976]","synonyms":"AQPap-3","biotype":"unprocessed_pseudogene","ncbi_id":"441432","summary":null,"start":65878766,"end":65894790,"strand":1,"description":"aquaporin 7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31976]"}, {"versioned_ensembl_gene_id":"ENSG00000112855.14","gene_symbol":"HARS2","gene_name":"histidyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:4817]","synonyms":"HO3,HARSR,HARSL","biotype":"protein_coding","ncbi_id":"23438","summary":"Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":140691426,"end":140699291,"strand":1,"description":"histidyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:4817]"}, {"versioned_ensembl_gene_id":"ENSG00000224049.1","gene_symbol":"AC108681.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187796187,"end":187805258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211839.1","gene_symbol":"TRAJ50","gene_name":"T-cell receptor alpha joining 50 [Source:HGNC Symbol;Acc:HGNC:12082]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28705","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22488593,"end":22488652,"strand":1,"description":"T-cell receptor alpha joining 50 [Source:HGNC Symbol;Acc:HGNC:12082]"}, {"versioned_ensembl_gene_id":"ENSG00000108622.10","gene_symbol":"ICAM2","gene_name":"intercellular adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:5345]","synonyms":"CD102","biotype":"protein_coding","ncbi_id":"3384","summary":"The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein may play a role in lymphocyte recirculation by blocking LFA-1-dependent cell adhesion. It mediates adhesive interactions important for antigen-specific immune response, NK-cell mediated clearance, lymphocyte recirculation, and other cellular interactions important for immune response and surveillance. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":64002594,"end":64020634,"strand":-1,"description":"intercellular adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:5345]"}, {"versioned_ensembl_gene_id":"ENSG00000264954.1","gene_symbol":"PRR29-AS1","gene_name":"PRR29 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51822]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400612","summary":null,"start":63996071,"end":63999899,"strand":-1,"description":"PRR29 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51822]"}, {"versioned_ensembl_gene_id":"ENSG00000226172.2","gene_symbol":"AL139420.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119000344,"end":119001392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174343.5","gene_symbol":"CHRNA9","gene_name":"cholinergic receptor nicotinic alpha 9 subunit [Source:HGNC Symbol;Acc:HGNC:14079]","synonyms":"NACHRA9","biotype":"protein_coding","ncbi_id":"55584","summary":"This gene is a member of the ligand-gated ionic channel family and nicotinic acetylcholine receptor gene superfamily. It encodes a plasma membrane protein that forms homo- or hetero-oligomeric divalent cation channels. This protein is involved in cochlea hair cell development and is also expressed in the outer hair cells (OHCs) of the adult cochlea. [provided by RefSeq, Feb 2012]","start":40335329,"end":40355217,"strand":1,"description":"cholinergic receptor nicotinic alpha 9 subunit [Source:HGNC Symbol;Acc:HGNC:14079]"}, {"versioned_ensembl_gene_id":"ENSG00000256720.1","gene_symbol":"BTG1P1","gene_name":"BTG anti-proliferation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37692]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129641","summary":null,"start":9135084,"end":9135591,"strand":1,"description":"BTG anti-proliferation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37692]"}, {"versioned_ensembl_gene_id":"ENSG00000274818.1","gene_symbol":"AC004825.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70906657,"end":70907111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275630.1","gene_symbol":"AC004816.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70822004,"end":70823984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092978.10","gene_symbol":"GPATCH2","gene_name":"G-patch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25499]","synonyms":"PPP1R30,Pfa1,GPATC2,FLJ10252,CT110","biotype":"protein_coding","ncbi_id":"55105","summary":"The gene encodes a nuclear factor that may play a role in spermatogenesis and in tumor growth during breast cancer. The encoded protein contains a G-patch domain with an RNA binding motif. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":217426992,"end":217631082,"strand":-1,"description":"G-patch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25499]"}, {"versioned_ensembl_gene_id":"ENSG00000226679.1","gene_symbol":"AL606748.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38221391,"end":38223667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213216.2","gene_symbol":"AC007066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123029373,"end":123029753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275500.1","gene_symbol":"GU182339.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54888671,"end":54903107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177238.13","gene_symbol":"TRIM72","gene_name":"tripartite motif containing 72 [Source:HGNC Symbol;Acc:HGNC:32671]","synonyms":"MG53","biotype":"protein_coding","ncbi_id":"493829","summary":null,"start":31214021,"end":31231537,"strand":1,"description":"tripartite motif containing 72 [Source:HGNC Symbol;Acc:HGNC:32671]"}, {"versioned_ensembl_gene_id":"ENSG00000136488.14","gene_symbol":"CSH1","gene_name":"chorionic somatomammotropin hormone 1 [Source:HGNC Symbol;Acc:HGNC:2440]","synonyms":"PL,hCS-A,FLJ75407,CSMT,CSA","biotype":"protein_coding","ncbi_id":"1442","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome. [provided by RefSeq, Jul 2008]","start":63894909,"end":63896661,"strand":-1,"description":"chorionic somatomammotropin hormone 1 [Source:HGNC Symbol;Acc:HGNC:2440]"}, {"versioned_ensembl_gene_id":"ENSG00000259998.1","gene_symbol":"AL133279.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88158240,"end":88160591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236497.1","gene_symbol":"LINC01744","gene_name":"long intergenic non-protein coding RNA 1744 [Source:HGNC Symbol;Acc:HGNC:52532]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927683","summary":null,"start":232727254,"end":232742715,"strand":-1,"description":"long intergenic non-protein coding RNA 1744 [Source:HGNC Symbol;Acc:HGNC:52532]"}, {"versioned_ensembl_gene_id":"ENSG00000235945.1","gene_symbol":"AC002543.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116873454,"end":116876376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255974.7","gene_symbol":"CYP2A6","gene_name":"cytochrome P450 family 2 subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:2610]","synonyms":"CYP2A3,CYP2A,CPA6","biotype":"protein_coding","ncbi_id":"1548","summary":"This gene, CYP2A6, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital. The enzyme is known to hydroxylate coumarin, and also metabolizes nicotine, aflatoxin B1, nitrosamines, and some pharmaceuticals. Individuals with certain allelic variants are said to have a poor metabolizer phenotype, meaning they do not efficiently metabolize coumarin or nicotine. This gene is part of a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. The gene was formerly referred to as CYP2A3; however, it has been renamed CYP2A6. [provided by RefSeq, Jul 2008]","start":40843538,"end":40850447,"strand":-1,"description":"cytochrome P450 family 2 subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:2610]"}, {"versioned_ensembl_gene_id":"ENSG00000128805.14","gene_symbol":"ARHGAP22","gene_name":"Rho GTPase activating protein 22 [Source:HGNC Symbol;Acc:HGNC:30320]","synonyms":"RhoGAP2","biotype":"protein_coding","ncbi_id":"58504","summary":"This gene encodes a member of the GTPase activating protein family which activates a GTPase belonging to the RAS superfamily of small GTP-binding proteins. The encoded protein is insulin-responsive, is dependent on the kinase Akt and requires the Akt-dependent 14-3-3 binding protein which binds sequentially to two serine residues. The result of these interactions is regulation of cell motility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":48446034,"end":48656265,"strand":-1,"description":"Rho GTPase activating protein 22 [Source:HGNC Symbol;Acc:HGNC:30320]"}, {"versioned_ensembl_gene_id":"ENSG00000211833.1","gene_symbol":"TRAJ58","gene_name":"T-cell receptor alpha joining 58 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12090]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28697","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22477707,"end":22477769,"strand":1,"description":"T-cell receptor alpha joining 58 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12090]"}, {"versioned_ensembl_gene_id":"ENSG00000116857.16","gene_symbol":"TMEM9","gene_name":"transmembrane protein 9 [Source:HGNC Symbol;Acc:HGNC:18823]","synonyms":"TMEM9A","biotype":"protein_coding","ncbi_id":"252839","summary":null,"start":201134772,"end":201171574,"strand":-1,"description":"transmembrane protein 9 [Source:HGNC Symbol;Acc:HGNC:18823]"}, {"versioned_ensembl_gene_id":"ENSG00000238270.1","gene_symbol":"AL591504.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189868001,"end":189868528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261359.2","gene_symbol":"PYCARD-AS1","gene_name":"PYCARD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45036]","synonyms":"PYCARDOS,C16orf98","biotype":"antisense_RNA","ncbi_id":"100652740","summary":null,"start":31201885,"end":31203452,"strand":1,"description":"PYCARD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45036]"}, {"versioned_ensembl_gene_id":"ENSG00000244738.1","gene_symbol":"AC026316.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":170656562,"end":170662123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175787.16","gene_symbol":"ZNF169","gene_name":"zinc finger protein 169 [Source:HGNC Symbol;Acc:HGNC:12957]","synonyms":"MGC51961","biotype":"protein_coding","ncbi_id":"169841","summary":null,"start":94259311,"end":94301454,"strand":1,"description":"zinc finger protein 169 [Source:HGNC Symbol;Acc:HGNC:12957]"}, {"versioned_ensembl_gene_id":"ENSG00000125084.11","gene_symbol":"WNT1","gene_name":"Wnt family member 1 [Source:HGNC Symbol;Acc:HGNC:12774]","synonyms":"INT1","biotype":"protein_coding","ncbi_id":"7471","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008]","start":48978453,"end":48981676,"strand":1,"description":"Wnt family member 1 [Source:HGNC Symbol;Acc:HGNC:12774]"}, {"versioned_ensembl_gene_id":"ENSG00000213285.4","gene_symbol":"RPL23AP45","gene_name":"ribosomal protein L23a pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36896]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729764","summary":null,"start":181471963,"end":181472430,"strand":1,"description":"ribosomal protein L23a pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36896]"}, {"versioned_ensembl_gene_id":"ENSG00000279186.1","gene_symbol":"FP236315.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":5703182,"end":5705637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220522.2","gene_symbol":"AL590002.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127416535,"end":127416952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260102.1","gene_symbol":"LINC01070","gene_name":"long intergenic non-protein coding RNA 1070 [Source:HGNC Symbol;Acc:HGNC:49110]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928698","summary":null,"start":112197350,"end":112201000,"strand":1,"description":"long intergenic non-protein coding RNA 1070 [Source:HGNC Symbol;Acc:HGNC:49110]"}, {"versioned_ensembl_gene_id":"ENSG00000008118.9","gene_symbol":"CAMK1G","gene_name":"calcium/calmodulin dependent protein kinase IG [Source:HGNC Symbol;Acc:HGNC:14585]","synonyms":"VWS1,dJ272L16.1,CLICKIII","biotype":"protein_coding","ncbi_id":"57172","summary":"This gene encodes a protein similar to calcium/calmodulin dependent protein kinase, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":209583717,"end":209613938,"strand":1,"description":"calcium/calmodulin dependent protein kinase IG [Source:HGNC Symbol;Acc:HGNC:14585]"}, {"versioned_ensembl_gene_id":"ENSG00000226590.1","gene_symbol":"UBE2V1P10","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:44895]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724605","summary":null,"start":85159682,"end":85159950,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:44895]"}, {"versioned_ensembl_gene_id":"ENSG00000258970.1","gene_symbol":"AC104002.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27418796,"end":27420735,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265693.1","gene_symbol":"AC026271.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18704640,"end":18704769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250957.1","gene_symbol":"AC012055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174135055,"end":174154637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236547.1","gene_symbol":"CR753864.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31604464,"end":31605043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249681.2","gene_symbol":"KRT19P3","gene_name":"keratin 19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33424]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442114","summary":null,"start":109879070,"end":109879897,"strand":-1,"description":"keratin 19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33424]"}, {"versioned_ensembl_gene_id":"ENSG00000253882.6","gene_symbol":"AC099548.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143761790,"end":143836933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279088.1","gene_symbol":"AC022400.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73742995,"end":73744230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256973.1","gene_symbol":"AC053513.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22460519,"end":22463914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231607.10","gene_symbol":"DLEU2","gene_name":"deleted in lymphocytic leukemia 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13748]","synonyms":"TRIM13OS,RFP2OS,NCRNA00022,MIR15AHG,LINC00022,LEU2,DLB2,BCMSUN","biotype":"antisense_RNA","ncbi_id":"8847","summary":"This locus represents a microRNA host gene and also produces long alternatively spliced non-coding RNAs. This genome region was observed to be deleted or epigenetically suppressed in leukemia, and was implicated as a negative regulator of cell proliferation. However, an alternative transcript produced at this locus was also found to promote progression through the cell cycle via angiotensin I converting enzyme 2 and cyclin D1. [provided by RefSeq, Dec 2017]","start":49982552,"end":50125720,"strand":-1,"description":"deleted in lymphocytic leukemia 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13748]"}, {"versioned_ensembl_gene_id":"ENSG00000223676.1","gene_symbol":"RPL34P26","gene_name":"ribosomal protein L34 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130718","summary":null,"start":50361410,"end":50361763,"strand":-1,"description":"ribosomal protein L34 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36100]"}, {"versioned_ensembl_gene_id":"ENSG00000234095.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30396057,"end":30396191,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000264207.1","gene_symbol":"AC239868.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149861271,"end":149862504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180071.19","gene_symbol":"ANKRD18A","gene_name":"ankyrin repeat domain 18A [Source:HGNC Symbol;Acc:HGNC:23643]","synonyms":"KIAA2015,FLJ35740","biotype":"protein_coding","ncbi_id":"253650","summary":null,"start":38571358,"end":38620660,"strand":-1,"description":"ankyrin repeat domain 18A [Source:HGNC Symbol;Acc:HGNC:23643]"}, {"versioned_ensembl_gene_id":"ENSG00000233379.1","gene_symbol":"AL139002.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77939162,"end":77944874,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262159.1","gene_symbol":"AC068305.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59027218,"end":59027943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253865.1","gene_symbol":"AC131025.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149372174,"end":149375116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224606.1","gene_symbol":"TGFA-IT1","gene_name":"TGFA intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41389]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874273","summary":null,"start":70467385,"end":70468495,"strand":-1,"description":"TGFA intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41389]"}, {"versioned_ensembl_gene_id":"ENSG00000224500.1","gene_symbol":"AL731575.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77313941,"end":77315694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251170.5","gene_symbol":"AC004052.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104230380,"end":104411035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225652.1","gene_symbol":"KCNMA1-AS3","gene_name":"KCNMA1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:51215]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929286","summary":null,"start":77354404,"end":77376613,"strand":1,"description":"KCNMA1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:51215]"}, {"versioned_ensembl_gene_id":"ENSG00000213976.4","gene_symbol":"AC010615.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21382865,"end":21387177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227284.2","gene_symbol":"MARK2P10","gene_name":"microtubule affinity regulating kinase 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402679","summary":null,"start":96858182,"end":96859618,"strand":1,"description":"microtubule affinity regulating kinase 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39801]"}, {"versioned_ensembl_gene_id":"ENSG00000260372.6","gene_symbol":"AQP4-AS1","gene_name":"AQP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26399]","synonyms":"CHST9-AS1,C18orf16,FLJ30507","biotype":"antisense_RNA","ncbi_id":"147429","summary":null,"start":26655742,"end":27190698,"strand":1,"description":"AQP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26399]"}, {"versioned_ensembl_gene_id":"ENSG00000182141.10","gene_symbol":"ZNF708","gene_name":"zinc finger protein 708 [Source:HGNC Symbol;Acc:HGNC:12945]","synonyms":"ZNF15L1,ZNF15,KOX8","biotype":"protein_coding","ncbi_id":"7562","summary":null,"start":21291160,"end":21329425,"strand":-1,"description":"zinc finger protein 708 [Source:HGNC Symbol;Acc:HGNC:12945]"}, {"versioned_ensembl_gene_id":"ENSG00000274161.4","gene_symbol":"DLGAP2","gene_name":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]","synonyms":"C8orf68,ERICH1-AS1,ERICH1-AS1,DAP2,DAP-2,C8orf68,SAPAP2","biotype":"protein_coding","ncbi_id":"9228","summary":"The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]","start":1501879,"end":1707457,"strand":1,"description":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]"}, {"versioned_ensembl_gene_id":"ENSG00000223723.1","gene_symbol":"BX842568.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36962196,"end":36963425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265948.1","gene_symbol":"AC015878.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21316878,"end":21317795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282977.1","gene_symbol":"PCBP2-OT1","gene_name":"PCBP2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49150]","synonyms":"TUC338","biotype":"non_coding","ncbi_id":"102157401","summary":null,"start":53464468,"end":53465057,"strand":1,"description":"PCBP2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49150]"}, {"versioned_ensembl_gene_id":"ENSG00000276230.4","gene_symbol":"RNH1","gene_name":"ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:10074]","synonyms":"RNH,RAI","biotype":"protein_coding","ncbi_id":"6050","summary":"Placental ribonuclease inhibitor (PRI) is a member of a family of proteinaceous cytoplasmic RNase inhibitors that occur in many tissues and bind to both intracellular and extracellular RNases (summarized by Lee et al., 1988 [PubMed 3219362]). In addition to control of intracellular RNases, the inhibitor may have a role in the regulation of angiogenin (MIM 105850). Ribonuclease inhibitor, of 50,000 Da, binds to ribonucleases and holds them in a latent form. Since neutral and alkaline ribonucleases probably play a critical role in the turnover of RNA in eukaryotic cells, RNH may be essential for control of mRNA turnover; the interaction of eukaryotic cells with ribonuclease may be reversible in vivo.[supplied by OMIM, Jul 2010]","start":494512,"end":507300,"strand":-1,"description":"ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:10074]"}, {"versioned_ensembl_gene_id":"ENSG00000223488.2","gene_symbol":"MAPK6PS2","gene_name":"mitogen-activated protein kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"254664","summary":null,"start":22436290,"end":22438349,"strand":-1,"description":"mitogen-activated protein kinase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16756]"}, {"versioned_ensembl_gene_id":"ENSG00000243116.1","gene_symbol":"AC092943.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159721524,"end":159722401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233132.4","gene_symbol":"FAM90A3P","gene_name":"family with sequence similarity 90 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32251]","synonyms":"FAM90A3","biotype":"unprocessed_pseudogene","ncbi_id":"389611","summary":"FAM90A3 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7264526,"end":7267536,"strand":1,"description":"family with sequence similarity 90 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32251]"}, {"versioned_ensembl_gene_id":"ENSG00000179627.9","gene_symbol":"ZBTB42","gene_name":"zinc finger and BTB domain containing 42 [Source:HGNC Symbol;Acc:HGNC:32550]","synonyms":"ZNF925","biotype":"protein_coding","ncbi_id":"100128927","summary":"The protein encoded by this gene is a member of the C2H2 zinc finger protein family. This protein is predicted to have a pox virus and zinc finger (POZ) domain at the N-terminus and four zinc finger domains at the C-terminus. In human and mouse, the protein localizes to the nuclei of skeletal muscle cells. Knockdown of this gene in zebrafish results in abnormal skeletal muscle development and myofibrillar disorganization. A novel homozygous variant of the human gene has been associated with lethal congenital contracture syndrome, an autosomal recessive disorder that results in muscle wasting. [provided by RefSeq, Mar 2015]","start":104800596,"end":104804712,"strand":1,"description":"zinc finger and BTB domain containing 42 [Source:HGNC Symbol;Acc:HGNC:32550]"}, {"versioned_ensembl_gene_id":"ENSG00000261187.1","gene_symbol":"AC079322.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72465128,"end":72466262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271560.1","gene_symbol":"AP001330.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101337496,"end":101337649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248444.1","gene_symbol":"HNRNPA1P65","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:48795]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481664","summary":null,"start":24771467,"end":24772420,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:48795]"}, {"versioned_ensembl_gene_id":"ENSG00000261121.1","gene_symbol":"LINC02473","gene_name":"long intergenic non-protein coding RNA 2473 [Source:HGNC Symbol;Acc:HGNC:53412]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986266","summary":null,"start":24659856,"end":24671568,"strand":1,"description":"long intergenic non-protein coding RNA 2473 [Source:HGNC Symbol;Acc:HGNC:53412]"}, {"versioned_ensembl_gene_id":"ENSG00000151327.12","gene_symbol":"FAM177A1","gene_name":"family with sequence similarity 177 member A1 [Source:HGNC Symbol;Acc:HGNC:19829]","synonyms":"C14orf24","biotype":"protein_coding","ncbi_id":"283635","summary":"This gene encodes a member of a conserved protein family. Alternative splicing results in multiple transcript variants. This gene is thought to be associated with susceptibility to juvenile idiopathic arthritis. [provided by RefSeq, Apr 2017]","start":35044907,"end":35113130,"strand":1,"description":"family with sequence similarity 177 member A1 [Source:HGNC Symbol;Acc:HGNC:19829]"}, {"versioned_ensembl_gene_id":"ENSG00000213366.12","gene_symbol":"GSTM2","gene_name":"glutathione S-transferase mu 2 [Source:HGNC Symbol;Acc:HGNC:4634]","synonyms":"GST4","biotype":"protein_coding","ncbi_id":"2946","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. [provided by RefSeq, Jul 2008]","start":109668022,"end":109709551,"strand":1,"description":"glutathione S-transferase mu 2 [Source:HGNC Symbol;Acc:HGNC:4634]"}, {"versioned_ensembl_gene_id":"ENSG00000181433.9","gene_symbol":"SAGE1","gene_name":"sarcoma antigen 1 [Source:HGNC Symbol;Acc:HGNC:30369]","synonyms":"SAGE,CT14","biotype":"protein_coding","ncbi_id":"55511","summary":"This gene belongs to a class of genes that are activated in tumors. These genes are expressed in tumors of different histologic types but not in normal tissues, except for spermatogenic cells and, for some, placenta. The proteins encoded by these genes appear to be strictly tumor specific, and hence may be excellent sources of antigens for cancer immunotherapy. This gene is expressed in sarcomas. [provided by RefSeq, Jul 2008]","start":135889205,"end":135913061,"strand":1,"description":"sarcoma antigen 1 [Source:HGNC Symbol;Acc:HGNC:30369]"}, {"versioned_ensembl_gene_id":"ENSG00000266227.1","gene_symbol":"AC016839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26204869,"end":26205904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234232.7","gene_symbol":"AC243772.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149676851,"end":149747818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237077.1","gene_symbol":"AC105399.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":77788382,"end":77793087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233842.1","gene_symbol":"AC062031.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145915090,"end":145931146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280255.1","gene_symbol":"AC004947.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":26538378,"end":26541048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271268.1","gene_symbol":"AC015849.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35861093,"end":35861566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122548.5","gene_symbol":"KIAA0087","gene_name":"KIAA0087 lncRNA [Source:HGNC Symbol;Acc:HGNC:22191]","synonyms":null,"biotype":"lincRNA","ncbi_id":"9808","summary":null,"start":26533121,"end":26538788,"strand":-1,"description":"KIAA0087 lncRNA [Source:HGNC Symbol;Acc:HGNC:22191]"}, {"versioned_ensembl_gene_id":"ENSG00000224929.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33059973,"end":33072108,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000163618.17","gene_symbol":"CADPS","gene_name":"calcium dependent secretion activator [Source:HGNC Symbol;Acc:HGNC:1426]","synonyms":"UNC-31,KIAA1121,CAPS1,CAPS","biotype":"protein_coding","ncbi_id":"8618","summary":"This gene encodes a novel neural/endocrine-specific cytosolic and peripheral membrane protein required for the Ca2+-regulated exocytosis of secretory vesicles. The protein acts at a stage in exocytosis that follows ATP-dependent priming, which involves the essential synthesis of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). Alternative splicing has been observed at this locus and three variants, encoding distinct isoforms, are described. [provided by RefSeq, Aug 2008]","start":62398346,"end":62875389,"strand":-1,"description":"calcium dependent secretion activator [Source:HGNC Symbol;Acc:HGNC:1426]"}, {"versioned_ensembl_gene_id":"ENSG00000234025.1","gene_symbol":"RBPMS2P1","gene_name":"RBPMS2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50509]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421512","summary":null,"start":73157517,"end":73158139,"strand":-1,"description":"RBPMS2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50509]"}, {"versioned_ensembl_gene_id":"ENSG00000253217.1","gene_symbol":"AP001574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100337595,"end":100350707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166833.19","gene_symbol":"NAV2","gene_name":"neuron navigator 2 [Source:HGNC Symbol;Acc:HGNC:15997]","synonyms":"RAINB1,POMFIL2,KIAA1419,HELAD1,FLJ23707,FLJ11030,FLJ10633","biotype":"protein_coding","ncbi_id":"89797","summary":"This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":19350724,"end":20121598,"strand":1,"description":"neuron navigator 2 [Source:HGNC Symbol;Acc:HGNC:15997]"}, {"versioned_ensembl_gene_id":"ENSG00000150269.1","gene_symbol":"OR5M9","gene_name":"olfactory receptor family 5 subfamily M member 9 [Source:HGNC Symbol;Acc:HGNC:15294]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390162","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56462469,"end":56463401,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 9 [Source:HGNC Symbol;Acc:HGNC:15294]"}, {"versioned_ensembl_gene_id":"ENSG00000272137.1","gene_symbol":"AL451064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79561132,"end":79561602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234653.1","gene_symbol":"AC079117.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76985965,"end":77009791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226218.1","gene_symbol":"AC079163.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145600907,"end":145603423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253179.1","gene_symbol":"CALCP","gene_name":"calcitonin pseudogene [Source:HGNC Symbol;Acc:HGNC:1439]","synonyms":"CALC3","biotype":"unprocessed_pseudogene","ncbi_id":"798","summary":null,"start":14907518,"end":14907986,"strand":1,"description":"calcitonin pseudogene [Source:HGNC Symbol;Acc:HGNC:1439]"}, {"versioned_ensembl_gene_id":"ENSG00000166866.12","gene_symbol":"MYO1A","gene_name":"myosin IA [Source:HGNC Symbol;Acc:HGNC:7595]","synonyms":"MYHL,DFNA48","biotype":"protein_coding","ncbi_id":"4640","summary":"This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011]","start":57028517,"end":57051198,"strand":-1,"description":"myosin IA [Source:HGNC Symbol;Acc:HGNC:7595]"}, {"versioned_ensembl_gene_id":"ENSG00000084636.17","gene_symbol":"COL16A1","gene_name":"collagen type XVI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2193]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1307","summary":"This gene encodes the alpha chain of type XVI collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Members of this collagen family are found in association with fibril-forming collagens such as type I and II, and serve to maintain the integrity of the extracellular matrix. High levels of type XVI collagen have been found in fibroblasts and keratinocytes, and in smooth muscle and amnion. [provided by RefSeq, Jul 2008]","start":31652247,"end":31704319,"strand":-1,"description":"collagen type XVI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2193]"}, {"versioned_ensembl_gene_id":"ENSG00000264078.1","gene_symbol":"AC114488.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31644694,"end":31649371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246898.1","gene_symbol":"LINC00920","gene_name":"long intergenic non-protein coding RNA 920 [Source:HGNC Symbol;Acc:HGNC:48611]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505865","summary":null,"start":66408524,"end":66412135,"strand":1,"description":"long intergenic non-protein coding RNA 920 [Source:HGNC Symbol;Acc:HGNC:48611]"}, {"versioned_ensembl_gene_id":"ENSG00000135363.11","gene_symbol":"LMO2","gene_name":"LIM domain only 2 [Source:HGNC Symbol;Acc:HGNC:6642]","synonyms":"TTG2,RHOM2,RBTNL1,RBTN2","biotype":"protein_coding","ncbi_id":"4005","summary":"LMO2 encodes a cysteine-rich, two LIM-domain protein that is required for yolk sac erythropoiesis. The LMO2 protein has a central and crucial role in hematopoietic development and is highly conserved. The LMO2 transcription start site is located approximately 25 kb downstream from the 11p13 T-cell translocation cluster (11p13 ttc), where a number T-cell acute lymphoblastic leukemia-specific translocations occur. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Nov 2008]","start":33858576,"end":33892289,"strand":-1,"description":"LIM domain only 2 [Source:HGNC Symbol;Acc:HGNC:6642]"}, {"versioned_ensembl_gene_id":"ENSG00000179271.2","gene_symbol":"GADD45GIP1","gene_name":"GADD45G interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29996]","synonyms":"PRG6,Plinp1,PLINP-1,MGC4758,MGC4667,CRIF1,CKbetaBP2,CKBBP2","biotype":"protein_coding","ncbi_id":"90480","summary":"This gene encodes a nuclear-localized protein that may be induced by p53 and regulates the cell cycle by inhibiting G1 to S phase progression. The encoded protein may interact with other cell cycle regulators. [provided by RefSeq, Aug 2012]","start":12953119,"end":12957236,"strand":-1,"description":"GADD45G interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29996]"}, {"versioned_ensembl_gene_id":"ENSG00000189319.13","gene_symbol":"FAM53B","gene_name":"family with sequence similarity 53 member B [Source:HGNC Symbol;Acc:HGNC:28968]","synonyms":"smp,KIAA0140,bA12J10.2","biotype":"protein_coding","ncbi_id":"9679","summary":null,"start":124619292,"end":124744269,"strand":-1,"description":"family with sequence similarity 53 member B [Source:HGNC Symbol;Acc:HGNC:28968]"}, {"versioned_ensembl_gene_id":"ENSG00000213365.3","gene_symbol":"AP000593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72280151,"end":72281178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166432.14","gene_symbol":"ZMAT1","gene_name":"zinc finger matrin-type 1 [Source:HGNC Symbol;Acc:HGNC:29377]","synonyms":"KIAA1789","biotype":"protein_coding","ncbi_id":"84460","summary":"This gene encodes a protein containing Cys2-His2 (C2H2)-type zinc fingers, which are similar to those found in the nuclear matrix protein matrin 3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":101882288,"end":101932031,"strand":-1,"description":"zinc finger matrin-type 1 [Source:HGNC Symbol;Acc:HGNC:29377]"}, {"versioned_ensembl_gene_id":"ENSG00000138346.14","gene_symbol":"DNA2","gene_name":"DNA replication helicase/nuclease 2 [Source:HGNC Symbol;Acc:HGNC:2939]","synonyms":"KIAA0083,DNA2L","biotype":"protein_coding","ncbi_id":"1763","summary":"This gene encodes a member of the DNA2/NAM7 helicase family. The encoded protein is a conserved helicase/nuclease involved in the maintenance of mitochondrial and nuclear DNA stability. Mutations in this gene are associated with autosomal dominant progressive external ophthalmoplegia-6 (PEOA6) and Seckel syndrome 8. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":68414064,"end":68472121,"strand":-1,"description":"DNA replication helicase/nuclease 2 [Source:HGNC Symbol;Acc:HGNC:2939]"}, {"versioned_ensembl_gene_id":"ENSG00000233327.10","gene_symbol":"USP32P2","gene_name":"ubiquitin specific peptidase 32 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30751]","synonyms":"TL132","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"220594","summary":null,"start":18511262,"end":18525930,"strand":-1,"description":"ubiquitin specific peptidase 32 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30751]"}, {"versioned_ensembl_gene_id":"ENSG00000221947.7","gene_symbol":"XKR9","gene_name":"XK related 9 [Source:HGNC Symbol;Acc:HGNC:20937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389668","summary":null,"start":70669365,"end":70790371,"strand":1,"description":"XK related 9 [Source:HGNC Symbol;Acc:HGNC:20937]"}, {"versioned_ensembl_gene_id":"ENSG00000179218.13","gene_symbol":"CALR","gene_name":"calreticulin [Source:HGNC Symbol;Acc:HGNC:1455]","synonyms":"SSA,RO,FLJ26680,CRT,cC1qR","biotype":"protein_coding","ncbi_id":"811","summary":"Calreticulin is a highly conserved chaperone protein which resides primarily in the endoplasmic reticulum, and is involved in a variety of cellular processes, among them, cell adhesion. Additionally, it functions in protein folding quality control and calcium homeostasis. Calreticulin is also found in the nucleus, suggesting that it may have a role in transcription regulation. Systemic lupus erythematosus is associated with increased autoantibody titers against calreticulin. Recurrent mutations in calreticulin have been linked to various neoplasms, including the myeloproliferative type.[provided by RefSeq, May 2020]","start":12938578,"end":12944489,"strand":1,"description":"calreticulin [Source:HGNC Symbol;Acc:HGNC:1455]"}, {"versioned_ensembl_gene_id":"ENSG00000224628.2","gene_symbol":"AL121723.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31285317,"end":31286835,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255461.1","gene_symbol":"OR8I1P","gene_name":"olfactory receptor family 8 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14828]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79498","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56296541,"end":56297471,"strand":-1,"description":"olfactory receptor family 8 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14828]"}, {"versioned_ensembl_gene_id":"ENSG00000276632.1","gene_symbol":"AL445528.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159649151,"end":159649620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132205.10","gene_symbol":"EMILIN2","gene_name":"elastin microfibril interfacer 2 [Source:HGNC Symbol;Acc:HGNC:19881]","synonyms":"FOAP-10,FLJ33200","biotype":"protein_coding","ncbi_id":"84034","summary":null,"start":2847030,"end":2915993,"strand":1,"description":"elastin microfibril interfacer 2 [Source:HGNC Symbol;Acc:HGNC:19881]"}, {"versioned_ensembl_gene_id":"ENSG00000236596.1","gene_symbol":"AC092568.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103494241,"end":103495842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182315.9","gene_symbol":"MBD3L3","gene_name":"methyl-CpG binding domain protein 3 like 3 [Source:HGNC Symbol;Acc:HGNC:37205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653657","summary":null,"start":7056209,"end":7058640,"strand":-1,"description":"methyl-CpG binding domain protein 3 like 3 [Source:HGNC Symbol;Acc:HGNC:37205]"}, {"versioned_ensembl_gene_id":"ENSG00000240111.1","gene_symbol":"BX927167.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28986766,"end":28988502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271329.1","gene_symbol":"AL035417.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44187943,"end":44189049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236673.5","gene_symbol":"AL117378.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131901963,"end":131920565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270798.1","gene_symbol":"AC018737.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121743479,"end":121745921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282907.1","gene_symbol":"Z98883.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":568837,"end":576257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233890.6","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31152269,"end":31157938,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000275023.4","gene_symbol":"MLLT6","gene_name":"MLLT6, PHD finger containing [Source:HGNC Symbol;Acc:HGNC:7138]","synonyms":"FLJ23480,AF17","biotype":"protein_coding","ncbi_id":"4302","summary":null,"start":38705542,"end":38729803,"strand":1,"description":"MLLT6, PHD finger containing [Source:HGNC Symbol;Acc:HGNC:7138]"}, {"versioned_ensembl_gene_id":"ENSG00000233457.1","gene_symbol":"AL353705.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78150532,"end":78151193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235269.1","gene_symbol":"LINC02331","gene_name":"long intergenic non-protein coding RNA 2331 [Source:HGNC Symbol;Acc:HGNC:53251]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370503","summary":null,"start":53768942,"end":53850882,"strand":-1,"description":"long intergenic non-protein coding RNA 2331 [Source:HGNC Symbol;Acc:HGNC:53251]"}, {"versioned_ensembl_gene_id":"ENSG00000231726.2","gene_symbol":"HMGN2P38","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39409]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874482","summary":null,"start":73580253,"end":73580517,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39409]"}, {"versioned_ensembl_gene_id":"ENSG00000241697.4","gene_symbol":"TMEFF1","gene_name":"transmembrane protein with EGF like and two follistatin like domains 1 [Source:HGNC Symbol;Acc:HGNC:11866]","synonyms":"H7365,CT120.1,C9orf2","biotype":"protein_coding","ncbi_id":"8577","summary":null,"start":100473113,"end":100577636,"strand":1,"description":"transmembrane protein with EGF like and two follistatin like domains 1 [Source:HGNC Symbol;Acc:HGNC:11866]"}, {"versioned_ensembl_gene_id":"ENSG00000153253.16","gene_symbol":"SCN3A","gene_name":"sodium voltage-gated channel alpha subunit 3 [Source:HGNC Symbol;Acc:HGNC:10590]","synonyms":"Nav1.3","biotype":"protein_coding","ncbi_id":"6328","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is found in a cluster of five alpha subunit genes on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":165087522,"end":165204067,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 3 [Source:HGNC Symbol;Acc:HGNC:10590]"}, {"versioned_ensembl_gene_id":"ENSG00000099957.16","gene_symbol":"P2RX6","gene_name":"purinergic receptor P2X 6 [Source:HGNC Symbol;Acc:HGNC:8538]","synonyms":"P2XM,P2X6,P2RXL1,MGC129625","biotype":"protein_coding","ncbi_id":"9127","summary":"The protein encoded by this gene belongs to the family of P2X receptors, which are ATP-gated ion channels and mediate rapid and selective permeability to cations. This gene is predominantly expressed in skeletal muscle, and regulated by p53. The encoded protein is associated with VE-cadherin at the adherens junctions of human umbilical vein endothelial cells. Alternative splicing results in multiple transcript variants. A related pseudogene, which is also located on chromosome 22, has been identified. [provided by RefSeq, Apr 2009]","start":21009808,"end":21028830,"strand":1,"description":"purinergic receptor P2X 6 [Source:HGNC Symbol;Acc:HGNC:8538]"}, {"versioned_ensembl_gene_id":"ENSG00000187535.13","gene_symbol":"IFT140","gene_name":"intraflagellar transport 140 [Source:HGNC Symbol;Acc:HGNC:29077]","synonyms":"gs114,WDTC2,KIAA0590","biotype":"protein_coding","ncbi_id":"9742","summary":"This gene encodes one of the subunits of the intraflagellar transport (IFT) complex A. Intraflagellar transport is involved in the genesis, resorption and signaling of primary cilia. The primary cilium is a microtubule-based sensory organelle at the surface of most quiescent mammalian cells, that receives signals from its environment, such as the flow of fluid, light or odors, and transduces those signals to the nucleus. Loss of the corresponding protein in mouse results in renal cystic disease. [provided by RefSeq, Jun 2012]","start":1510427,"end":1612110,"strand":-1,"description":"intraflagellar transport 140 [Source:HGNC Symbol;Acc:HGNC:29077]"}, {"versioned_ensembl_gene_id":"ENSG00000101200.5","gene_symbol":"AVP","gene_name":"arginine vasopressin [Source:HGNC Symbol;Acc:HGNC:894]","synonyms":"ARVP,ADH","biotype":"protein_coding","ncbi_id":"551","summary":"This gene encodes a member of the vasopressin/oxytocin family and preproprotein that is proteolytically processed to generate multiple protein products. These products include the neuropeptide hormone arginine vasopressin, and two other peptides, neurophysin 2 and copeptin. Arginine vasopressin is a posterior pituitary hormone that is synthesized in the supraoptic nucleus and paraventricular nucleus of the hypothalamus. Along with its carrier protein, neurophysin 2, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis where it is either stored or secreted into the bloodstream. The precursor is thought to be activated while it is being transported along the axon to the posterior pituitary. Arginine vasopressin acts as a growth factor by enhancing pH regulation through acid-base transport systems. It has a direct antidiuretic action on the kidney, and also causes vasoconstriction of the peripheral vessels. This hormone can contract smooth muscle during parturition and lactation. It is also involved in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. Mutations in this gene cause autosomal dominant neurohypophyseal diabetes insipidus (ADNDI). This gene is present in a gene cluster with the related gene oxytocin on chromosome 20. [provided by RefSeq, Nov 2015]","start":3082556,"end":3084724,"strand":-1,"description":"arginine vasopressin [Source:HGNC Symbol;Acc:HGNC:894]"}, {"versioned_ensembl_gene_id":"ENSG00000261018.1","gene_symbol":"AC002101.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133611798,"end":133633099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068137.14","gene_symbol":"PLEKHH3","gene_name":"pleckstrin homology, MyTH4 and FERM domain containing H3 [Source:HGNC Symbol;Acc:HGNC:26105]","synonyms":"FLJ21019","biotype":"protein_coding","ncbi_id":"79990","summary":null,"start":42667914,"end":42676994,"strand":-1,"description":"pleckstrin homology, MyTH4 and FERM domain containing H3 [Source:HGNC Symbol;Acc:HGNC:26105]"}, {"versioned_ensembl_gene_id":"ENSG00000138069.16","gene_symbol":"RAB1A","gene_name":"RAB1A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9758]","synonyms":"YPT1,RAB1","biotype":"protein_coding","ncbi_id":"5861","summary":"This gene encodes a member of the Ras superfamily of GTPases. Members of the gene family cycle between inactive GDP-bound and active GTP-bound forms. This small GTPase controls vesicle traffic from the endoplasmic reticulum to the Golgi apparatus. Multiple alternatively spliced transcript variants have been identified for this gene which encode different protein isoforms. [provided by RefSeq, Oct 2008]","start":65070701,"end":65130106,"strand":-1,"description":"RAB1A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9758]"}, {"versioned_ensembl_gene_id":"ENSG00000279793.1","gene_symbol":"AP000676.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87816999,"end":87817567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279701.1","gene_symbol":"AP003497.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87490144,"end":87491110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206042.1","gene_symbol":"DEFA7P","gene_name":"defensin alpha 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31798]","synonyms":"DEFA7","biotype":"unprocessed_pseudogene","ncbi_id":"724067","summary":null,"start":7038571,"end":7039439,"strand":-1,"description":"defensin alpha 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31798]"}, {"versioned_ensembl_gene_id":"ENSG00000054967.12","gene_symbol":"RELT","gene_name":"RELT, TNF receptor [Source:HGNC Symbol;Acc:HGNC:13764]","synonyms":"TNFRSF19L,FLJ14993","biotype":"protein_coding","ncbi_id":"84957","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is especially abundant in hematologic tissues. It has been shown to activate the NF-kappaB pathway and selectively bind TNF receptor-associated factor 1 (TRAF1). This receptor is capable of stimulating T-cell proliferation in the presence of CD3 signaling, which suggests its regulatory role in immune response. Two alternatively spliced transcript variants of this gene encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":73376264,"end":73397474,"strand":1,"description":"RELT, TNF receptor [Source:HGNC Symbol;Acc:HGNC:13764]"}, {"versioned_ensembl_gene_id":"ENSG00000236745.2","gene_symbol":"YRDCP2","gene_name":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128237","summary":null,"start":96954820,"end":96955461,"strand":1,"description":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39920]"}, {"versioned_ensembl_gene_id":"ENSG00000227257.1","gene_symbol":"AL158827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96918928,"end":96919318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228807.1","gene_symbol":"MRPS18CP6","gene_name":"mitochondrial ribosomal protein S18C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29747]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343901","summary":null,"start":44483495,"end":44483717,"strand":-1,"description":"mitochondrial ribosomal protein S18C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:29747]"}, {"versioned_ensembl_gene_id":"ENSG00000227466.1","gene_symbol":"AL590783.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66042500,"end":66050718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232655.1","gene_symbol":"LINC01656","gene_name":"long intergenic non-protein coding RNA 1656 [Source:HGNC Symbol;Acc:HGNC:52444]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927526","summary":null,"start":44443327,"end":44444788,"strand":1,"description":"long intergenic non-protein coding RNA 1656 [Source:HGNC Symbol;Acc:HGNC:52444]"}, {"versioned_ensembl_gene_id":"ENSG00000267189.1","gene_symbol":"AC067852.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42647834,"end":42648143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270587.1","gene_symbol":"AC046185.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63610772,"end":63611184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258419.1","gene_symbol":"AC022469.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79199982,"end":79201632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269688.1","gene_symbol":"AC008982.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38844729,"end":38845499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261691.1","gene_symbol":"Z97986.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":547185,"end":553847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103326.11","gene_symbol":"CAPN15","gene_name":"calpain 15 [Source:HGNC Symbol;Acc:HGNC:11182]","synonyms":"SOLH","biotype":"protein_coding","ncbi_id":"6650","summary":"This gene encodes a protein containing zinc-finger-like repeats and a calpain-like protease domain. The encoded protein may function as a transcription factor, RNA-binding protein, or in protein-protein interactions during visual system development. [provided by RefSeq, Jul 2008]","start":527717,"end":554636,"strand":1,"description":"calpain 15 [Source:HGNC Symbol;Acc:HGNC:11182]"}, {"versioned_ensembl_gene_id":"ENSG00000256783.1","gene_symbol":"AC079031.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132457160,"end":132460024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254804.1","gene_symbol":"AP006437.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55684141,"end":55686160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217327.3","gene_symbol":"RPS7P5","gene_name":"ribosomal protein S7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645884","summary":null,"start":240012646,"end":240013226,"strand":1,"description":"ribosomal protein S7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37037]"}, {"versioned_ensembl_gene_id":"ENSG00000005059.15","gene_symbol":"MCUB","gene_name":"mitochondrial calcium uniporter dominant negative beta subunit [Source:HGNC Symbol;Acc:HGNC:26076]","synonyms":"FLJ20647,CCDC109B","biotype":"protein_coding","ncbi_id":"55013","summary":null,"start":109560205,"end":109688726,"strand":1,"description":"mitochondrial calcium uniporter dominant negative beta subunit [Source:HGNC Symbol;Acc:HGNC:26076]"}, {"versioned_ensembl_gene_id":"ENSG00000169247.11","gene_symbol":"SH3TC2","gene_name":"SH3 domain and tetratricopeptide repeats 2 [Source:HGNC Symbol;Acc:HGNC:29427]","synonyms":"KIAA1985,CMT4C","biotype":"protein_coding","ncbi_id":"79628","summary":"This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons. [provided by RefSeq, Jul 2008]","start":148923639,"end":149063163,"strand":-1,"description":"SH3 domain and tetratricopeptide repeats 2 [Source:HGNC Symbol;Acc:HGNC:29427]"}, {"versioned_ensembl_gene_id":"ENSG00000138944.7","gene_symbol":"KIAA1644","gene_name":"KIAA1644 [Source:HGNC Symbol;Acc:HGNC:29335]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85352","summary":null,"start":44243667,"end":44312851,"strand":-1,"description":"KIAA1644 [Source:HGNC Symbol;Acc:HGNC:29335]"}, {"versioned_ensembl_gene_id":"ENSG00000254576.2","gene_symbol":"OR4C1P","gene_name":"olfactory receptor family 4 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8292]","synonyms":"OR4C1,HTPCRX11,HSHTPCRX11","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26242","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55506635,"end":55511169,"strand":1,"description":"olfactory receptor family 4 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8292]"}, {"versioned_ensembl_gene_id":"ENSG00000267007.1","gene_symbol":"AC012615.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1815249,"end":1815873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265222.1","gene_symbol":"AC079336.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32509954,"end":32523424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206026.7","gene_symbol":"SMIM21","gene_name":"small integral membrane protein 21 [Source:HGNC Symbol;Acc:HGNC:27598]","synonyms":"C18orf62","biotype":"protein_coding","ncbi_id":"284274","summary":null,"start":75409476,"end":75427703,"strand":-1,"description":"small integral membrane protein 21 [Source:HGNC Symbol;Acc:HGNC:27598]"}, {"versioned_ensembl_gene_id":"ENSG00000226377.1","gene_symbol":"AC084809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32876759,"end":32878637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271133.5","gene_symbol":"AC004130.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20328299,"end":20331747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226097.5","gene_symbol":"AC099342.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20296708,"end":20311712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158428.3","gene_symbol":"CATIP","gene_name":"ciliogenesis associated TTC17 interacting protein [Source:HGNC Symbol;Acc:HGNC:25062]","synonyms":"MGC50811,C2orf62","biotype":"protein_coding","ncbi_id":"375307","summary":null,"start":218356856,"end":218368099,"strand":1,"description":"ciliogenesis associated TTC17 interacting protein [Source:HGNC Symbol;Acc:HGNC:25062]"}, {"versioned_ensembl_gene_id":"ENSG00000274797.1","gene_symbol":"AC008121.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50953924,"end":50954356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270734.1","gene_symbol":"AC136443.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14862380,"end":14862749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231019.1","gene_symbol":"AL354896.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88142867,"end":88236082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148482.11","gene_symbol":"SLC39A12","gene_name":"solute carrier family 39 member 12 [Source:HGNC Symbol;Acc:HGNC:20860]","synonyms":"FLJ30499","biotype":"protein_coding","ncbi_id":"221074","summary":"Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A12 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Aug 2008]","start":17951839,"end":18043292,"strand":1,"description":"solute carrier family 39 member 12 [Source:HGNC Symbol;Acc:HGNC:20860]"}, {"versioned_ensembl_gene_id":"ENSG00000169490.16","gene_symbol":"TM2D2","gene_name":"TM2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24127]","synonyms":"BLP1","biotype":"protein_coding","ncbi_id":"83877","summary":"The protein encoded by this gene contains a structural module related to that of the seven transmembrane domain G protein-coupled receptor superfamily. This protein has sequence and structural similarities to the beta-amyloid binding protein (BBP), but, unlike BBP, it does not regulate a response to beta-amyloid peptide. This protein may have regulatory roles in cell death or proliferation signal cascades. This gene has multiple alternatively spliced transcript variants which encode two different isoforms. [provided by RefSeq, Jul 2008]","start":38988808,"end":38996824,"strand":-1,"description":"TM2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24127]"}, {"versioned_ensembl_gene_id":"ENSG00000235160.1","gene_symbol":"LINC02248","gene_name":"long intergenic non-protein coding RNA 2248 [Source:HGNC Symbol;Acc:HGNC:53147]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984780","summary":null,"start":26395072,"end":26446774,"strand":1,"description":"long intergenic non-protein coding RNA 2248 [Source:HGNC Symbol;Acc:HGNC:53147]"}, {"versioned_ensembl_gene_id":"ENSG00000184730.10","gene_symbol":"APOBR","gene_name":"apolipoprotein B receptor [Source:HGNC Symbol;Acc:HGNC:24087]","synonyms":"APOB48R,APOB100R","biotype":"protein_coding","ncbi_id":"55911","summary":"Apolipoprotein B48 receptor is a macrophage receptor that binds to the apolipoprotein B48 of dietary triglyceride (TG)-rich lipoproteins. This receptor may provide essential lipids, lipid-soluble vitamins and other nutrients to reticuloendothelial cells. If overwhelmed with elevated plasma triglyceride, the apolipoprotein B48 receptor may contribute to foam cell formation, endothelial dysfunction, and atherothrombogenesis. [provided by RefSeq, Jul 2008]","start":28494649,"end":28498970,"strand":1,"description":"apolipoprotein B receptor [Source:HGNC Symbol;Acc:HGNC:24087]"}, {"versioned_ensembl_gene_id":"ENSG00000260629.1","gene_symbol":"BGLT3","gene_name":"beta globin locus transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49033]","synonyms":"lncRNA-BGL3,LINC01083,BGL3","biotype":"sense_overlapping","ncbi_id":"103344929","summary":null,"start":5244554,"end":5245547,"strand":-1,"description":"beta globin locus transcript 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49033]"}, {"versioned_ensembl_gene_id":"ENSG00000215467.2","gene_symbol":"AL121886.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43652523,"end":43653291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067208.14","gene_symbol":"EVI5","gene_name":"ecotropic viral integration site 5 [Source:HGNC Symbol;Acc:HGNC:3501]","synonyms":"NB4S","biotype":"protein_coding","ncbi_id":"7813","summary":null,"start":92508696,"end":92792404,"strand":-1,"description":"ecotropic viral integration site 5 [Source:HGNC Symbol;Acc:HGNC:3501]"}, {"versioned_ensembl_gene_id":"ENSG00000150672.16","gene_symbol":"DLG2","gene_name":"discs large MAGUK scaffold protein 2 [Source:HGNC Symbol;Acc:HGNC:2901]","synonyms":"PSD93,PSD-93,PPP1R58,chapsyn-110","biotype":"protein_coding","ncbi_id":"1740","summary":"This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. The encoded protein forms a heterodimer with a related family member that may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described, but their full-length nature is not known. [provided by RefSeq, Dec 2008]","start":83455012,"end":85627922,"strand":-1,"description":"discs large MAGUK scaffold protein 2 [Source:HGNC Symbol;Acc:HGNC:2901]"}, {"versioned_ensembl_gene_id":"ENSG00000255396.2","gene_symbol":"AP000857.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84997226,"end":84997768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267834.1","gene_symbol":"AL592211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129004502,"end":129004998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236217.4","gene_symbol":"C1DP2","gene_name":"C1D nuclear receptor corepressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31660]","synonyms":"bA369J21.3","biotype":"processed_pseudogene","ncbi_id":"642538","summary":null,"start":80031968,"end":80032393,"strand":-1,"description":"C1D nuclear receptor corepressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31660]"}, {"versioned_ensembl_gene_id":"ENSG00000224760.4","gene_symbol":"C1DP3","gene_name":"C1D nuclear receptor corepressor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31661]","synonyms":"bA369J21.2","biotype":"processed_pseudogene","ncbi_id":"642521","summary":null,"start":80024737,"end":80025159,"strand":-1,"description":"C1D nuclear receptor corepressor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31661]"}, {"versioned_ensembl_gene_id":"ENSG00000256972.1","gene_symbol":"AP000462.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115333577,"end":115340262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224195.1","gene_symbol":"AC022400.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73813518,"end":73814737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167985.6","gene_symbol":"SDHAF2","gene_name":"succinate dehydrogenase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:26034]","synonyms":"SDH5,PGL2,FLJ20487,C11orf79","biotype":"protein_coding","ncbi_id":"54949","summary":"This gene encodes a mitochondrial protein needed for the flavination of a succinate dehydrogenase complex subunit required for activity of the complex. Mutations in this gene are associated with paraganglioma.[provided by RefSeq, Jul 2010]","start":61430042,"end":61447529,"strand":1,"description":"succinate dehydrogenase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:26034]"}, {"versioned_ensembl_gene_id":"ENSG00000270259.2","gene_symbol":"BX255925.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137286112,"end":137287236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174469.19","gene_symbol":"CNTNAP2","gene_name":"contactin associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13830]","synonyms":"NRXN4,KIAA0868,Caspr2","biotype":"protein_coding","ncbi_id":"26047","summary":"This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and is also involved in localization of potassium channels within differentiating axons. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by forkhead box protein P2, a transcription factor related to speech and language development. This gene has been implicated in multiple neurodevelopmental disorders, including Gilles de la Tourette syndrome, schizophrenia, epilepsy, autism, ADHD and intellectual disability. [provided by RefSeq, Jul 2017]","start":146116002,"end":148420998,"strand":1,"description":"contactin associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13830]"}, {"versioned_ensembl_gene_id":"ENSG00000188612.11","gene_symbol":"SUMO2","gene_name":"small ubiquitin-like modifier 2 [Source:HGNC Symbol;Acc:HGNC:11125]","synonyms":"SMT3H2,SMT3B","biotype":"protein_coding","ncbi_id":"6613","summary":"This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last two amino acids of the carboxy-terminus have been cleaved off. Numerous pseudogenes have been reported for this gene. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":75165586,"end":75182983,"strand":-1,"description":"small ubiquitin-like modifier 2 [Source:HGNC Symbol;Acc:HGNC:11125]"}, {"versioned_ensembl_gene_id":"ENSG00000253672.1","gene_symbol":"AC105177.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116402543,"end":116403757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196169.14","gene_symbol":"KIF19","gene_name":"kinesin family member 19 [Source:HGNC Symbol;Acc:HGNC:26735]","synonyms":"KIF19A,FLJ37300","biotype":"protein_coding","ncbi_id":"124602","summary":null,"start":74326210,"end":74355820,"strand":1,"description":"kinesin family member 19 [Source:HGNC Symbol;Acc:HGNC:26735]"}, {"versioned_ensembl_gene_id":"ENSG00000182040.8","gene_symbol":"USH1G","gene_name":"USH1 protein network component sans [Source:HGNC Symbol;Acc:HGNC:16356]","synonyms":"Sans,FLJ33924,ANKS4A","biotype":"protein_coding","ncbi_id":"124590","summary":"This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":74916084,"end":74923256,"strand":-1,"description":"USH1 protein network component sans [Source:HGNC Symbol;Acc:HGNC:16356]"}, {"versioned_ensembl_gene_id":"ENSG00000101052.12","gene_symbol":"IFT52","gene_name":"intraflagellar transport 52 [Source:HGNC Symbol;Acc:HGNC:15901]","synonyms":"NGD5,NGD2,dJ1028D15.1,CGI-53,C20orf9","biotype":"protein_coding","ncbi_id":"51098","summary":"This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]","start":43590931,"end":43647296,"strand":1,"description":"intraflagellar transport 52 [Source:HGNC Symbol;Acc:HGNC:15901]"}, {"versioned_ensembl_gene_id":"ENSG00000280259.1","gene_symbol":"AL512662.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79970963,"end":79973213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283130.1","gene_symbol":"AL445984.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88571654,"end":88572312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242600.8","gene_symbol":"MBL1P","gene_name":"mannose binding lectin 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:6921]","synonyms":"MBL1P1,COLEC3P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"8512","summary":null,"start":79920178,"end":79923119,"strand":1,"description":"mannose binding lectin 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:6921]"}, {"versioned_ensembl_gene_id":"ENSG00000163682.15","gene_symbol":"RPL9","gene_name":"ribosomal protein L9 [Source:HGNC Symbol;Acc:HGNC:10369]","synonyms":"L9","biotype":"protein_coding","ncbi_id":"6133","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L6P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":39454124,"end":39458948,"strand":-1,"description":"ribosomal protein L9 [Source:HGNC Symbol;Acc:HGNC:10369]"}, {"versioned_ensembl_gene_id":"ENSG00000113492.13","gene_symbol":"AGXT2","gene_name":"alanine--glyoxylate aminotransferase 2 [Source:HGNC Symbol;Acc:HGNC:14412]","synonyms":"AGT2","biotype":"protein_coding","ncbi_id":"64902","summary":"The protein encoded by this gene is a class III pyridoxal-phosphate-dependent mitochondrial aminotransferase. It catalyzes the conversion of glyoxylate to glycine using L-alanine as the amino donor. It is an important regulator of methylarginines and is involved in the control of blood pressure in kidney. Polymorphisms in this gene affect methylarginine and beta-aminoisobutyrate metabolism, and are associated with carotid atherosclerosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":34998101,"end":35048135,"strand":-1,"description":"alanine--glyoxylate aminotransferase 2 [Source:HGNC Symbol;Acc:HGNC:14412]"}, {"versioned_ensembl_gene_id":"ENSG00000136114.15","gene_symbol":"THSD1","gene_name":"thrombospondin type 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17754]","synonyms":"TMTSP","biotype":"protein_coding","ncbi_id":"55901","summary":"The protein encoded by this gene contains a type 1 thrombospondin domain, which is found in a number of proteins involved in the complement pathway, as well as in extracellular matrix proteins. Alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Jan 2009]","start":52377167,"end":52406494,"strand":-1,"description":"thrombospondin type 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17754]"}, {"versioned_ensembl_gene_id":"ENSG00000106236.3","gene_symbol":"NPTX2","gene_name":"neuronal pentraxin 2 [Source:HGNC Symbol;Acc:HGNC:7953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4885","summary":"This gene encodes a member of the family of neuronal petraxins, synaptic proteins that are related to C-reactive protein. This protein is involved in excitatory synapse formation. It also plays a role in clustering of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors at established synapses, resulting in non-apoptotic cell death of dopaminergic nerve cells. Up-regulation of this gene in Parkinson disease (PD) tissues suggests that the protein may be involved in the pathology of PD. [provided by RefSeq, Feb 2009]","start":98617297,"end":98629868,"strand":1,"description":"neuronal pentraxin 2 [Source:HGNC Symbol;Acc:HGNC:7953]"}, {"versioned_ensembl_gene_id":"ENSG00000224415.1","gene_symbol":"AC007683.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103141349,"end":103141939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232677.6","gene_symbol":"LINC00665","gene_name":"long intergenic non-protein coding RNA 665 [Source:HGNC Symbol;Acc:HGNC:44323]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506930","summary":null,"start":36313067,"end":36331718,"strand":-1,"description":"long intergenic non-protein coding RNA 665 [Source:HGNC Symbol;Acc:HGNC:44323]"}, {"versioned_ensembl_gene_id":"ENSG00000102309.12","gene_symbol":"PIN4","gene_name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4 [Source:HGNC Symbol;Acc:HGNC:8992]","synonyms":"PAR17,PAR14,EPVH","biotype":"protein_coding","ncbi_id":"5303","summary":"This gene encodes a member of the parvulin subfamily of the peptidyl-prolyl cis/trans isomerase protein family. The encoded protein catalyzes the isomerization of peptidylprolyl bonds, and may play a role in the cell cycle, chromatin remodeling, and/or ribosome biogenesis. The encoded protein may play an additional role in the mitochondria. [provided by RefSeq, Dec 2009]","start":72181353,"end":72302926,"strand":1,"description":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4 [Source:HGNC Symbol;Acc:HGNC:8992]"}, {"versioned_ensembl_gene_id":"ENSG00000213830.3","gene_symbol":"CFL1P5","gene_name":"cofilin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1877]","synonyms":"CFLP5,CFLL1","biotype":"processed_pseudogene","ncbi_id":"1074","summary":null,"start":69313371,"end":69313872,"strand":-1,"description":"cofilin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1877]"}, {"versioned_ensembl_gene_id":"ENSG00000282598.1","gene_symbol":"AC138374.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":668204,"end":680202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282712.1","gene_symbol":"DEAF1","gene_name":"DEAF1, transcription factor [Source:HGNC Symbol;Acc:HGNC:14677]","synonyms":"ZMYND5,SPN,NUDR","biotype":"protein_coding","ncbi_id":"10522","summary":"This gene encodes a zinc finger domain-containing protein that functions as a regulator of transcription. The encoded proteins binds to its own promoter as well as to that of several target genes. Activity of this protein is important in the regulation of embryonic development. Mutations in this gene have been found in individuals with autosomal dominant cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":646472,"end":677067,"strand":-1,"description":"DEAF1, transcription factor [Source:HGNC Symbol;Acc:HGNC:14677]"}, {"versioned_ensembl_gene_id":"ENSG00000216817.1","gene_symbol":"R3HDM2P2","gene_name":"R3H domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44057]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129694","summary":null,"start":104017633,"end":104019748,"strand":-1,"description":"R3H domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44057]"}, {"versioned_ensembl_gene_id":"ENSG00000198670.11","gene_symbol":"LPA","gene_name":"lipoprotein(a) [Source:HGNC Symbol;Acc:HGNC:6667]","synonyms":"Lp(a),LP","biotype":"protein_coding","ncbi_id":"4018","summary":"The protein encoded by this gene is a serine proteinase that inhibits the activity of tissue-type plasminogen activator I. The encoded protein constitutes a substantial portion of lipoprotein(a) and is proteolytically cleaved, resulting in fragments that attach to atherosclerotic lesions and promote thrombogenesis. Elevated plasma levels of this protein are linked to atherosclerosis. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type domains. The allele represented here contains 15 copies of the kringle-type repeats and corresponds to that found in the reference genome sequence. [provided by RefSeq, Dec 2009]","start":160531483,"end":160664259,"strand":-1,"description":"lipoprotein(a) [Source:HGNC Symbol;Acc:HGNC:6667]"}, {"versioned_ensembl_gene_id":"ENSG00000283413.1","gene_symbol":"AC008703.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159484130,"end":159511687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198034.10","gene_symbol":"RPS4X","gene_name":"ribosomal protein S4, X-linked [Source:HGNC Symbol;Acc:HGNC:10424]","synonyms":"S4,RPS4,FLJ40595,DXS306,CCG2,SCR10,SCAR","biotype":"protein_coding","ncbi_id":"6191","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes ribosomal protein S4, a component of the 40S subunit. Ribosomal protein S4 is the only ribosomal protein known to be encoded by more than one gene, namely this gene and ribosomal protein S4, Y-linked (RPS4Y). The 2 isoforms encoded by these genes are not identical, but are functionally equivalent. Ribosomal protein S4 belongs to the S4E family of ribosomal proteins. This gene is not subject to X-inactivation. It has been suggested that haploinsufficiency of the ribosomal protein S4 genes plays a role in Turner syndrome; however, this hypothesis is controversial. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":72255679,"end":72277300,"strand":-1,"description":"ribosomal protein S4, X-linked [Source:HGNC Symbol;Acc:HGNC:10424]"}, {"versioned_ensembl_gene_id":"ENSG00000178974.9","gene_symbol":"FBXO34","gene_name":"F-box protein 34 [Source:HGNC Symbol;Acc:HGNC:20201]","synonyms":"FLJ20725,Fbx34","biotype":"protein_coding","ncbi_id":"55030","summary":"Members of the F-box protein family, such as FBXO34, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":55271303,"end":55361918,"strand":1,"description":"F-box protein 34 [Source:HGNC Symbol;Acc:HGNC:20201]"}, {"versioned_ensembl_gene_id":"ENSG00000282731.1","gene_symbol":"AC138747.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28416342,"end":28416567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235238.1","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"dJ271M21,SMT3H2P,SUMO2P,SMT3Bp","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29636060,"end":29636343,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000236330.1","gene_symbol":"RPL5P9","gene_name":"ribosomal protein L5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270832","summary":null,"start":110967834,"end":110968719,"strand":1,"description":"ribosomal protein L5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36557]"}, {"versioned_ensembl_gene_id":"ENSG00000213443.2","gene_symbol":"AC007068.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9695384,"end":9696227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143761.15","gene_symbol":"ARF1","gene_name":"ADP ribosylation factor 1 [Source:HGNC Symbol;Acc:HGNC:652]","synonyms":null,"biotype":"protein_coding","ncbi_id":"375","summary":"ADP-ribosylation factor 1 (ARF1) is a member of the human ARF gene family. The family members encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking as activators of phospholipase D. The gene products, including 6 ARF proteins and 11 ARF-like proteins, constitute a family of the RAS superfamily. The ARF proteins are categorized as class I (ARF1, ARF2 and ARF3), class II (ARF4 and ARF5) and class III (ARF6), and members of each class share a common gene organization. The ARF1 protein is localized to the Golgi apparatus and has a central role in intra-Golgi transport. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":228082660,"end":228099212,"strand":1,"description":"ADP ribosylation factor 1 [Source:HGNC Symbol;Acc:HGNC:652]"}, {"versioned_ensembl_gene_id":"ENSG00000225085.1","gene_symbol":"AL162726.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82405188,"end":82406239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230746.1","gene_symbol":"AC006007.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145675882,"end":145681369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231839.1","gene_symbol":"AC073055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145583197,"end":145584817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254391.1","gene_symbol":"AC011363.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160685351,"end":160692889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273847.1","gene_symbol":"AC139494.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69766913,"end":69768768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205352.10","gene_symbol":"PRR13","gene_name":"proline rich 13 [Source:HGNC Symbol;Acc:HGNC:24528]","synonyms":"FLJ23818,DKFZP564J157","biotype":"protein_coding","ncbi_id":"54458","summary":null,"start":53441605,"end":53446645,"strand":1,"description":"proline rich 13 [Source:HGNC Symbol;Acc:HGNC:24528]"}, {"versioned_ensembl_gene_id":"ENSG00000230894.1","gene_symbol":"AL133284.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116568449,"end":116586328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268047.1","gene_symbol":"AC018766.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49852887,"end":49854967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000054392.12","gene_symbol":"HHAT","gene_name":"hedgehog acyltransferase [Source:HGNC Symbol;Acc:HGNC:18270]","synonyms":"FLJ10724,Skn,ski,sit,rasp,MART2,MART-2,GUP2","biotype":"protein_coding","ncbi_id":"55733","summary":"'Skinny hedgehog' (SKI1) encodes an enzyme that acts within the secretory pathway to catalyze amino-terminal palmitoylation of 'hedgehog' (see MIM 600725).[supplied by OMIM, Jul 2002]","start":210328252,"end":210676296,"strand":1,"description":"hedgehog acyltransferase [Source:HGNC Symbol;Acc:HGNC:18270]"}, {"versioned_ensembl_gene_id":"ENSG00000258013.2","gene_symbol":"RPL3P13","gene_name":"ribosomal protein L3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48494]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480199","summary":null,"start":84544304,"end":84544519,"strand":-1,"description":"ribosomal protein L3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48494]"}, {"versioned_ensembl_gene_id":"ENSG00000284698.1","gene_symbol":"AC084121.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7686423,"end":7686643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172803.17","gene_symbol":"SNX32","gene_name":"sorting nexin 32 [Source:HGNC Symbol;Acc:HGNC:26423]","synonyms":"SNX6B,FLJ30934","biotype":"protein_coding","ncbi_id":"254122","summary":null,"start":65833641,"end":65856896,"strand":1,"description":"sorting nexin 32 [Source:HGNC Symbol;Acc:HGNC:26423]"}, {"versioned_ensembl_gene_id":"ENSG00000267340.1","gene_symbol":"AC060780.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43169880,"end":43170077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164611.12","gene_symbol":"PTTG1","gene_name":"pituitary tumor-transforming 1 [Source:HGNC Symbol;Acc:HGNC:9690]","synonyms":"TUTR1,securin,PTTG,HPTTG,EAP1","biotype":"protein_coding","ncbi_id":"9232","summary":"The encoded protein is a homolog of yeast securin proteins, which prevent separins from promoting sister chromatid separation. It is an anaphase-promoting complex (APC) substrate that associates with a separin until activation of the APC. The gene product has transforming activity in vitro and tumorigenic activity in vivo, and the gene is highly expressed in various tumors. The gene product contains 2 PXXP motifs, which are required for its transforming and tumorigenic activities, as well as for its stimulation of basic fibroblast growth factor expression. It also contains a destruction box (D box) that is required for its degradation by the APC. The acidic C-terminal region of the encoded protein can act as a transactivation domain. The gene product is mainly a cytosolic protein, although it partially localizes in the nucleus. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013]","start":160421822,"end":160428744,"strand":1,"description":"pituitary tumor-transforming 1 [Source:HGNC Symbol;Acc:HGNC:9690]"}, {"versioned_ensembl_gene_id":"ENSG00000125686.11","gene_symbol":"MED1","gene_name":"mediator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:9234]","synonyms":"TRIP2,TRAP220,RB18A,PPARGBP,PPARBP,PBP,DRIP230,CRSP200,CRSP1","biotype":"protein_coding","ncbi_id":"5469","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. It also regulates p53-dependent apoptosis and it is essential for adipogenesis. This protein is known to have the ability to self-oligomerize. [provided by RefSeq, Jul 2008]","start":39404285,"end":39451286,"strand":-1,"description":"mediator complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:9234]"}, {"versioned_ensembl_gene_id":"ENSG00000119718.10","gene_symbol":"EIF2B2","gene_name":"eukaryotic translation initiation factor 2B subunit beta [Source:HGNC Symbol;Acc:HGNC:3258]","synonyms":"EIF2B,EIF-2Bbeta","biotype":"protein_coding","ncbi_id":"8892","summary":"This gene encodes the beta subunit of eukaryotic initiation factor-2B (EIF2B). EIF2B is involved in protein synthesis and exchanges GDP and GTP for its activation and deactivation. [provided by RefSeq, Aug 2011]","start":75002911,"end":75012366,"strand":1,"description":"eukaryotic translation initiation factor 2B subunit beta [Source:HGNC Symbol;Acc:HGNC:3258]"}, {"versioned_ensembl_gene_id":"ENSG00000277977.1","gene_symbol":"AC010332.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52392659,"end":52392755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283525.1","gene_symbol":"AC005622.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43690002,"end":43700508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219665.8","gene_symbol":"AC008770.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":11987617,"end":12046275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255120.5","gene_symbol":"OVOL1-AS1","gene_name":"OVOL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49319]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927828","summary":null,"start":65789051,"end":65790868,"strand":-1,"description":"OVOL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49319]"}, {"versioned_ensembl_gene_id":"ENSG00000006453.13","gene_symbol":"BAIAP2L1","gene_name":"BAI1 associated protein 2 like 1 [Source:HGNC Symbol;Acc:HGNC:21649]","synonyms":"IRTKS","biotype":"protein_coding","ncbi_id":"55971","summary":"This gene encodes a member of the IMD (IRSp53/MIM homology domain) family. Members of this family can be subdivided in two groups, the IRSp53-like and MIM-like, based on the presence or absence of the SH3 (Src homology 3) domain. The protein encoded by this gene contains a conserved IMD, also known as F-actin bundling domain, at the N-terminus, and a canonical SH3 domain near the C-terminus, so it belongs to the IRSp53-like group. This protein is the substrate for insulin receptor tyrosine kinase and binds to the small GTPase Rac. It is involved in signal transduction pathways that link deformation of the plasma membrane and remodeling of the actin cytoskeleton. It also promotes actin assembly and membrane protrusions when overexpressed in mammalian cells, and is essential to the formation of a potent actin assembly complex during EHEC (Enterohemorrhagic Escherichia coli) pedestal formation. [provided by RefSeq, Oct 2009]","start":98291651,"end":98401068,"strand":-1,"description":"BAI1 associated protein 2 like 1 [Source:HGNC Symbol;Acc:HGNC:21649]"}, {"versioned_ensembl_gene_id":"ENSG00000262952.1","gene_symbol":"AC139099.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83211996,"end":83221190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178734.5","gene_symbol":"LMO7DN","gene_name":"LMO7 downstream neighbor [Source:HGNC Symbol;Acc:HGNC:44370]","synonyms":"C13orf45","biotype":"protein_coding","ncbi_id":"729420","summary":null,"start":75871038,"end":75883811,"strand":1,"description":"LMO7 downstream neighbor [Source:HGNC Symbol;Acc:HGNC:44370]"}, {"versioned_ensembl_gene_id":"ENSG00000264647.1","gene_symbol":"AC104564.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29591703,"end":29592241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271621.1","gene_symbol":"AC013244.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50847925,"end":50848312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282208.1","gene_symbol":"AC229888.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142602235,"end":142602743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249196.6","gene_symbol":"TMEM132D-AS1","gene_name":"TMEM132D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27466]","synonyms":"LOC283352","biotype":"antisense_RNA","ncbi_id":"283352","summary":null,"start":129109629,"end":129113294,"strand":1,"description":"TMEM132D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27466]"}, {"versioned_ensembl_gene_id":"ENSG00000255379.1","gene_symbol":"CYCSP29","gene_name":"cytochrome c, somatic pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:24403]","synonyms":"HCP29","biotype":"processed_pseudogene","ncbi_id":"360180","summary":null,"start":108822333,"end":108822650,"strand":-1,"description":"cytochrome c, somatic pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:24403]"}, {"versioned_ensembl_gene_id":"ENSG00000150556.16","gene_symbol":"LYPD6B","gene_name":"LY6/PLAUR domain containing 6B [Source:HGNC Symbol;Acc:HGNC:27018]","synonyms":"LYPD7,CT116","biotype":"protein_coding","ncbi_id":"130576","summary":null,"start":149038107,"end":149215262,"strand":1,"description":"LY6/PLAUR domain containing 6B [Source:HGNC Symbol;Acc:HGNC:27018]"}, {"versioned_ensembl_gene_id":"ENSG00000282242.1","gene_symbol":"AC229888.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142596665,"end":142597147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230804.2","gene_symbol":"C2orf27AP3","gene_name":"chromosome 2 open reading frame 27A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50418]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420784","summary":null,"start":40121962,"end":40122540,"strand":1,"description":"chromosome 2 open reading frame 27A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50418]"}, {"versioned_ensembl_gene_id":"ENSG00000101335.9","gene_symbol":"MYL9","gene_name":"myosin light chain 9 [Source:HGNC Symbol;Acc:HGNC:15754]","synonyms":"MYRL2,MRLC1,MLC2,LC20","biotype":"protein_coding","ncbi_id":"10398","summary":"Myosin, a structural component of muscle, consists of two heavy chains and four light chains. The protein encoded by this gene is a myosin light chain that may regulate muscle contraction by modulating the ATPase activity of myosin heads. The encoded protein binds calcium and is activated by myosin light chain kinase. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":36541484,"end":36551447,"strand":1,"description":"myosin light chain 9 [Source:HGNC Symbol;Acc:HGNC:15754]"}, {"versioned_ensembl_gene_id":"ENSG00000206284.8","gene_symbol":"WDR46","gene_name":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]","synonyms":"BING4,UTP7,C6orf11","biotype":"protein_coding","ncbi_id":"9277","summary":null,"start":33207935,"end":33218358,"strand":-1,"description":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]"}, {"versioned_ensembl_gene_id":"ENSG00000240509.1","gene_symbol":"RPL34P18","gene_name":"ribosomal protein L34 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271003","summary":null,"start":93957338,"end":93957691,"strand":-1,"description":"ribosomal protein L34 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:35968]"}, {"versioned_ensembl_gene_id":"ENSG00000272281.6","gene_symbol":"TPTE2P2","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38076]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644623","summary":null,"start":52219344,"end":52334277,"strand":-1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38076]"}, {"versioned_ensembl_gene_id":"ENSG00000145743.15","gene_symbol":"FBXL17","gene_name":"F-box and leucine rich repeat protein 17 [Source:HGNC Symbol;Acc:HGNC:13615]","synonyms":"FBXO13,Fbx13,Fbl17,DKFZP434C1715","biotype":"protein_coding","ncbi_id":"64839","summary":"Members of the F-box protein family, such as FBXL17, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":107859035,"end":108382098,"strand":-1,"description":"F-box and leucine rich repeat protein 17 [Source:HGNC Symbol;Acc:HGNC:13615]"}, {"versioned_ensembl_gene_id":"ENSG00000259624.1","gene_symbol":"AC009269.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70768011,"end":70778868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261544.1","gene_symbol":"AC011939.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65766460,"end":65767398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228001.8","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30126032,"end":30138662,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000176927.15","gene_symbol":"EFCAB5","gene_name":"EF-hand calcium binding domain 5 [Source:HGNC Symbol;Acc:HGNC:24801]","synonyms":"FLJ46247","biotype":"protein_coding","ncbi_id":"374786","summary":null,"start":29929200,"end":30108452,"strand":1,"description":"EF-hand calcium binding domain 5 [Source:HGNC Symbol;Acc:HGNC:24801]"}, {"versioned_ensembl_gene_id":"ENSG00000221931.2","gene_symbol":"OR6X1","gene_name":"olfactory receptor family 6 subfamily X member 1 [Source:HGNC Symbol;Acc:HGNC:14737]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390260","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123753488,"end":123754545,"strand":-1,"description":"olfactory receptor family 6 subfamily X member 1 [Source:HGNC Symbol;Acc:HGNC:14737]"}, {"versioned_ensembl_gene_id":"ENSG00000196352.14","gene_symbol":"CD55","gene_name":"CD55 molecule (Cromer blood group) [Source:HGNC Symbol;Acc:HGNC:2665]","synonyms":"TC,DAF,CROM,CR","biotype":"protein_coding","ncbi_id":"1604","summary":"This gene encodes a glycoprotein involved in the regulation of the complement cascade. Binding of the encoded protein to complement proteins accelerates their decay, thereby disrupting the cascade and preventing damage to host cells. Antigens present on this protein constitute the Cromer blood group system (CROM). Alternative splicing results in multiple transcript variants. The predominant transcript variant encodes a membrane-bound protein, but alternatively spliced transcripts may produce soluble proteins. [provided by RefSeq, Jul 2014]","start":207321508,"end":207386804,"strand":1,"description":"CD55 molecule (Cromer blood group) [Source:HGNC Symbol;Acc:HGNC:2665]"}, {"versioned_ensembl_gene_id":"ENSG00000180210.14","gene_symbol":"F2","gene_name":"coagulation factor II, thrombin [Source:HGNC Symbol;Acc:HGNC:3535]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2147","summary":"This gene encodes the prothrombin protein (also known as coagulation factor II). This protein is proteolytically cleaved in multiple steps to form the activated serine protease thrombin. The activated thrombin enzyme plays an important role in thrombosis and hemostasis by converting fibrinogen to fibrin during blood clot formation, by stimulating platelet aggregation, and by activating additional coagulation factors. Thrombin also plays a role in cell proliferation, tissue repair, and angiogenesis as well as maintaining vascular integrity during development and postnatal life. Peptides derived from the C-terminus of this protein have antimicrobial activity against E. coli and P. aeruginosa. Mutations in this gene lead to various forms of thrombosis and dysprothrombinemia. Rapid increases in cytokine levels following coronavirus infections can dysregulate the coagulation cascade and produce thrombosis, compromised blood supply, and organ failure. [provided by RefSeq, May 2020]","start":46719180,"end":46739506,"strand":1,"description":"coagulation factor II, thrombin [Source:HGNC Symbol;Acc:HGNC:3535]"}, {"versioned_ensembl_gene_id":"ENSG00000167733.13","gene_symbol":"HSD11B1L","gene_name":"hydroxysteroid 11-beta dehydrogenase 1 like [Source:HGNC Symbol;Acc:HGNC:30419]","synonyms":"SDR26C2,SCDR10","biotype":"protein_coding","ncbi_id":"374875","summary":"This gene is a member of the hydroxysteroid dehydrogenase family. The encoded protein is similar to an enzyme that catalyzes the interconversion of inactive to active glucocorticoids (e.g. cortisone). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012]","start":5680604,"end":5688523,"strand":1,"description":"hydroxysteroid 11-beta dehydrogenase 1 like [Source:HGNC Symbol;Acc:HGNC:30419]"}, {"versioned_ensembl_gene_id":"ENSG00000278031.2","gene_symbol":"CU024913.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54574401,"end":54580112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234740.1","gene_symbol":"AL162386.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":13274510,"end":13279187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204348.9","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31969810,"end":31972292,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000070961.15","gene_symbol":"ATP2B1","gene_name":"ATPase plasma membrane Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:814]","synonyms":"PMCA1","biotype":"protein_coding","ncbi_id":"490","summary":"The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 1. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":89588049,"end":89709300,"strand":-1,"description":"ATPase plasma membrane Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:814]"}, {"versioned_ensembl_gene_id":"ENSG00000178796.12","gene_symbol":"RIIAD1","gene_name":"regulatory subunit of type II PKA R-subunit (RIIa) domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26686]","synonyms":"NCRNA00166,FLJ36032,C1orf230","biotype":"protein_coding","ncbi_id":"284485","summary":null,"start":151710433,"end":151729805,"strand":1,"description":"regulatory subunit of type II PKA R-subunit (RIIa) domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26686]"}, {"versioned_ensembl_gene_id":"ENSG00000215037.2","gene_symbol":"VENTXP2","gene_name":"VENT homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287345","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the VENT homeobox gene family [provided by RefSeq, Mar 2013]","start":83907301,"end":83907781,"strand":-1,"description":"VENT homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30901]"}, {"versioned_ensembl_gene_id":"ENSG00000106263.17","gene_symbol":"EIF3B","gene_name":"eukaryotic translation initiation factor 3 subunit B [Source:HGNC Symbol;Acc:HGNC:3280]","synonyms":"PRT1,EIF3S9,eIF3b","biotype":"protein_coding","ncbi_id":"8662","summary":null,"start":2354086,"end":2380745,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit B [Source:HGNC Symbol;Acc:HGNC:3280]"}, {"versioned_ensembl_gene_id":"ENSG00000164185.5","gene_symbol":"ZNF474","gene_name":"zinc finger protein 474 [Source:HGNC Symbol;Acc:HGNC:23245]","synonyms":"FLJ32921,4933409D10Rik","biotype":"protein_coding","ncbi_id":"133923","summary":null,"start":122129513,"end":122153571,"strand":1,"description":"zinc finger protein 474 [Source:HGNC Symbol;Acc:HGNC:23245]"}, {"versioned_ensembl_gene_id":"ENSG00000278532.1","gene_symbol":"AC026585.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69398726,"end":69399249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254057.1","gene_symbol":"AC084346.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93834454,"end":93846743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224490.5","gene_symbol":"TTC21B-AS1","gene_name":"TTC21B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41115]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506134","summary":null,"start":165933857,"end":165949891,"strand":1,"description":"TTC21B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41115]"}, {"versioned_ensembl_gene_id":"ENSG00000225428.1","gene_symbol":"NDUFB4P7","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45255]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075094","summary":null,"start":87968609,"end":87968971,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45255]"}, {"versioned_ensembl_gene_id":"ENSG00000256206.2","gene_symbol":"AC018523.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14493783,"end":14520344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165970.11","gene_symbol":"SLC6A5","gene_name":"solute carrier family 6 member 5 [Source:HGNC Symbol;Acc:HGNC:11051]","synonyms":"NET1,GLYT2","biotype":"protein_coding","ncbi_id":"9152","summary":"This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":20599400,"end":20659285,"strand":1,"description":"solute carrier family 6 member 5 [Source:HGNC Symbol;Acc:HGNC:11051]"}, {"versioned_ensembl_gene_id":"ENSG00000230606.10","gene_symbol":"AC092683.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97416165,"end":97433527,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164764.10","gene_symbol":"SBSPON","gene_name":"somatomedin B and thrombospondin type 1 domain containing [Source:HGNC Symbol;Acc:HGNC:30362]","synonyms":"RPESP,C8orf84","biotype":"protein_coding","ncbi_id":"157869","summary":null,"start":73064540,"end":73124088,"strand":-1,"description":"somatomedin B and thrombospondin type 1 domain containing [Source:HGNC Symbol;Acc:HGNC:30362]"}, {"versioned_ensembl_gene_id":"ENSG00000234195.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29307588,"end":29308553,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000270204.1","gene_symbol":"AC020549.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114517864,"end":114518371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242737.1","gene_symbol":"AC012170.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50466738,"end":50467096,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204961.6","gene_symbol":"PCDHA9","gene_name":"protocadherin alpha 9 [Source:HGNC Symbol;Acc:HGNC:8675]","synonyms":"PCDH-ALPHA9,KIAA0345","biotype":"protein_coding","ncbi_id":"9752","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140847463,"end":141012344,"strand":1,"description":"protocadherin alpha 9 [Source:HGNC Symbol;Acc:HGNC:8675]"}, {"versioned_ensembl_gene_id":"ENSG00000152409.8","gene_symbol":"JMY","gene_name":"junction mediating and regulatory protein, p53 cofactor [Source:HGNC Symbol;Acc:HGNC:28916]","synonyms":"WHAMM2,FLJ37870","biotype":"protein_coding","ncbi_id":"133746","summary":null,"start":79236189,"end":79327215,"strand":1,"description":"junction mediating and regulatory protein, p53 cofactor [Source:HGNC Symbol;Acc:HGNC:28916]"}, {"versioned_ensembl_gene_id":"ENSG00000177239.14","gene_symbol":"MAN1B1","gene_name":"mannosidase alpha class 1B member 1 [Source:HGNC Symbol;Acc:HGNC:6823]","synonyms":"MRT15,MANA-ER,ERManI","biotype":"protein_coding","ncbi_id":"11253","summary":"This gene encodes an enzyme belonging to the glycosyl hydrolase 47 family. This enzyme functions in N-glycan biosynthesis, and is a class I alpha-1,2-mannosidase that specifically converts Man9GlcNAc to Man8GlcNAc isomer B. It is required for N-glycan trimming to Man5-6GlcNAc2 in the endoplasmic-reticulum-associated degradation pathway. Mutations in this gene cause autosomal-recessive intellectual disability. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Dec 2011]","start":137086927,"end":137109187,"strand":1,"description":"mannosidase alpha class 1B member 1 [Source:HGNC Symbol;Acc:HGNC:6823]"}, {"versioned_ensembl_gene_id":"ENSG00000259298.1","gene_symbol":"AC012170.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50497195,"end":50498744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279684.1","gene_symbol":"AP003969.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93286629,"end":93288903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232621.1","gene_symbol":"C4BPAP2","gene_name":"complement component 4 binding protein, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1327]","synonyms":"C4BPAL2","biotype":"unprocessed_pseudogene","ncbi_id":"724","summary":null,"start":207225798,"end":207229202,"strand":1,"description":"complement component 4 binding protein, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1327]"}, {"versioned_ensembl_gene_id":"ENSG00000253147.5","gene_symbol":"AC015468.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20953127,"end":20968904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243989.8","gene_symbol":"ACY1","gene_name":"aminoacylase 1 [Source:HGNC Symbol;Acc:HGNC:177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"95","summary":"This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Nov 2010]","start":51983278,"end":51989202,"strand":1,"description":"aminoacylase 1 [Source:HGNC Symbol;Acc:HGNC:177]"}, {"versioned_ensembl_gene_id":"ENSG00000155393.12","gene_symbol":"HEATR3","gene_name":"HEAT repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:26087]","synonyms":"FLJ20718","biotype":"protein_coding","ncbi_id":"55027","summary":"The protein encoded by this gene plays a role in ribosomal protein transport and in the assembly of the 5S ribonucleoprotein particle (5S RNP). The encoded protein also may be involved in NOD2-mediated NF-kappaB signaling. [provided by RefSeq, Jul 2016]","start":50065941,"end":50106387,"strand":1,"description":"HEAT repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:26087]"}, {"versioned_ensembl_gene_id":"ENSG00000232467.2","gene_symbol":"TMA16P2","gene_name":"translation machinery associated 16 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101407","summary":null,"start":45846994,"end":45847594,"strand":-1,"description":"translation machinery associated 16 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43781]"}, {"versioned_ensembl_gene_id":"ENSG00000253866.1","gene_symbol":"TMEM97P2","gene_name":"transmembrane protein 97 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39641]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"724059","summary":null,"start":20934435,"end":20934837,"strand":-1,"description":"transmembrane protein 97 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39641]"}, {"versioned_ensembl_gene_id":"ENSG00000232949.1","gene_symbol":"AC002480.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22589705,"end":22591622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261189.1","gene_symbol":"AL031058.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7540451,"end":7541338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196353.11","gene_symbol":"CPNE4","gene_name":"copine 4 [Source:HGNC Symbol;Acc:HGNC:2317]","synonyms":"CPN4,COPN4","biotype":"protein_coding","ncbi_id":"131034","summary":"This gene belongs to the highly conserved copine family. It encodes a calcium-dependent, phospholipid-binding protein, which may be involved in membrane trafficking, mitogenesis and development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":131533555,"end":132285410,"strand":-1,"description":"copine 4 [Source:HGNC Symbol;Acc:HGNC:2317]"}, {"versioned_ensembl_gene_id":"ENSG00000101049.14","gene_symbol":"SGK2","gene_name":"SGK2, serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:13900]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10110","summary":"This gene encodes a serine/threonine protein kinase. Although this gene product is similar to serum- and glucocorticoid-induced protein kinase (SGK), this gene is not induced by serum or glucocorticoids. This gene is induced in response to signals that activate phosphatidylinositol 3-kinase, which is also true for SGK. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":43558968,"end":43588237,"strand":1,"description":"SGK2, serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:13900]"}, {"versioned_ensembl_gene_id":"ENSG00000224897.6","gene_symbol":"POT1-AS1","gene_name":"POT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49459]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"401398","summary":null,"start":124929873,"end":125179315,"strand":1,"description":"POT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49459]"}, {"versioned_ensembl_gene_id":"ENSG00000248383.4","gene_symbol":"PCDHAC1","gene_name":"protocadherin alpha subfamily C, 1 [Source:HGNC Symbol;Acc:HGNC:8676]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56135","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140926369,"end":141012344,"strand":1,"description":"protocadherin alpha subfamily C, 1 [Source:HGNC Symbol;Acc:HGNC:8676]"}, {"versioned_ensembl_gene_id":"ENSG00000198129.2","gene_symbol":"DEFB107B","gene_name":"defensin beta 107B [Source:HGNC Symbol;Acc:HGNC:31918]","synonyms":"HsT21816","biotype":"protein_coding","ncbi_id":"503614","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 107, DEFB107A and DEFB107B, in tail-to-tail orientation. This gene, DEFB107B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7495846,"end":7509311,"strand":1,"description":"defensin beta 107B [Source:HGNC Symbol;Acc:HGNC:31918]"}, {"versioned_ensembl_gene_id":"ENSG00000283546.1","gene_symbol":"BX088723.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21131496,"end":21163726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226975.1","gene_symbol":"AC006987.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10169788,"end":10170314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225592.1","gene_symbol":"BX248084.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29216117,"end":29217054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189280.3","gene_symbol":"GJB5","gene_name":"gap junction protein beta 5 [Source:HGNC Symbol;Acc:HGNC:4287]","synonyms":"CX31.1","biotype":"protein_coding","ncbi_id":"2709","summary":"This gene encodes a member of the beta-type (group I) connexin family. The encoded protein is a gap junction protein involved in intercellular communication related to epidermal differentiation and environmental sensing. This gene has been linked to non-small cell lung cancer. [provided by RefSeq, Nov 2012]","start":34755047,"end":34758512,"strand":1,"description":"gap junction protein beta 5 [Source:HGNC Symbol;Acc:HGNC:4287]"}, {"versioned_ensembl_gene_id":"ENSG00000141562.17","gene_symbol":"NARF","gene_name":"nuclear prelamin A recognition factor [Source:HGNC Symbol;Acc:HGNC:29916]","synonyms":"IOP2,DKFZp434G0420,FLJ10067","biotype":"protein_coding","ncbi_id":"26502","summary":"Several proteins have been found to be prenylated and methylated at their carboxyl-terminal ends. Prenylation was initially believed to be important only for membrane attachment. However, another role for prenylation appears to be its importance in protein-protein interactions. The only nuclear proteins known to be prenylated in mammalian cells are prelamin A- and B-type lamins. Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif. This post-translationally modified cysteine residue is removed from prelamin A when it is endoproteolytically processed into mature lamin A. The protein encoded by this gene binds to the prenylated prelamin A carboxyl-terminal tail domain. It may be a component of a prelamin A endoprotease complex. The encoded protein is located in the nucleus, where it partially colocalizes with the nuclear lamina. It shares limited sequence similarity with iron-only bacterial hydrogenases. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene, including one with a novel exon that is generated by RNA editing. [provided by RefSeq, Jul 2008]","start":82458180,"end":82490537,"strand":1,"description":"nuclear prelamin A recognition factor [Source:HGNC Symbol;Acc:HGNC:29916]"}, {"versioned_ensembl_gene_id":"ENSG00000022556.15","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1,CLR19.9,NBS1,FLJ20510","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54953130,"end":55001142,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000282097.1","gene_symbol":"AL160408.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234709383,"end":234720220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248530.1","gene_symbol":"BCL2L12P1","gene_name":"BCL2 like 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51327]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289095","summary":null,"start":131526447,"end":131527179,"strand":1,"description":"BCL2 like 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51327]"}, {"versioned_ensembl_gene_id":"ENSG00000138081.20","gene_symbol":"FBXO11","gene_name":"F-box protein 11 [Source:HGNC Symbol;Acc:HGNC:13590]","synonyms":"UBR6,FBX11","biotype":"protein_coding","ncbi_id":"80204","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. It can function as an arginine methyltransferase that symmetrically dimethylates arginine residues, and it acts as an adaptor protein to mediate the neddylation of p53, which leads to the suppression of p53 function. This gene is known to be down-regulated in melanocytes from patients with vitiligo, a skin disorder that results in depigmentation. Polymorphisms in this gene are associated with chronic otitis media with effusion and recurrent otitis media (COME/ROM), a hearing loss disorder, and the knockout of the homologous mouse gene results in the deaf mouse mutant Jeff (Jf), a single gene model of otitis media. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]","start":47789316,"end":47905793,"strand":-1,"description":"F-box protein 11 [Source:HGNC Symbol;Acc:HGNC:13590]"}, {"versioned_ensembl_gene_id":"ENSG00000249958.1","gene_symbol":"CCT7P2","gene_name":"chaperonin containing TCP1 subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288772","summary":null,"start":92889387,"end":92890840,"strand":-1,"description":"chaperonin containing TCP1 subunit 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35134]"}, {"versioned_ensembl_gene_id":"ENSG00000235684.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"TAT-SF1-L,HTATSF1P,dJ1033B10.6","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33166626,"end":33168528,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000186810.7","gene_symbol":"CXCR3","gene_name":"C-X-C motif chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:4540]","synonyms":"CD183,MigR,IP10-R,GPR9,CMKAR3,CKR-L2","biotype":"protein_coding","ncbi_id":"2833","summary":"This gene encodes a G protein-coupled receptor with selectivity for three chemokines, termed CXCL9/Mig (monokine induced by interferon-g), CXCL10/IP10 (interferon-g-inducible 10 kDa protein) and CXCL11/I-TAC (interferon-inducible T cell a-chemoattractant). Binding of chemokines to this protein induces cellular responses that are involved in leukocyte traffic, most notably integrin activation, cytoskeletal changes and chemotactic migration. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. One of the isoforms (CXCR3-B) shows high affinity binding to chemokine, CXCL4/PF4 (PMID:12782716). [provided by RefSeq, Jun 2011]","start":71615916,"end":71618517,"strand":-1,"description":"C-X-C motif chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:4540]"}, {"versioned_ensembl_gene_id":"ENSG00000267194.1","gene_symbol":"AC002546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69551358,"end":69553861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227862.1","gene_symbol":"HNRNPA1P31","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39549]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506925","summary":null,"start":80619098,"end":80620067,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39549]"}, {"versioned_ensembl_gene_id":"ENSG00000271015.1","gene_symbol":"IGKV2OR2-7D","gene_name":"immunoglobulin kappa variable 2/OR2-7D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37489]","synonyms":"IGKV2/OR2-7D","biotype":"IG_V_pseudogene","ncbi_id":"100310869","summary":null,"start":97335671,"end":97335974,"strand":-1,"description":"immunoglobulin kappa variable 2/OR2-7D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37489]"}, {"versioned_ensembl_gene_id":"ENSG00000232073.1","gene_symbol":"Z82198.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33164063,"end":33166439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089063.14","gene_symbol":"TMEM230","gene_name":"transmembrane protein 230 [Source:HGNC Symbol;Acc:HGNC:15876]","synonyms":"HSPC274,C20orf30","biotype":"protein_coding","ncbi_id":"29058","summary":"This gene encodes a multi-pass transmembrane protein that belongs to the TMEM134/TMEM230 protein family. The encoded protein localizes to secretory and recycling vesicle in the neuron and may be involved in synaptic vesicles trafficking and recycling. Mutations in this gene may be linked to familial Parkinson's disease. [provided by RefSeq, Mar 2017]","start":5068232,"end":5113103,"strand":-1,"description":"transmembrane protein 230 [Source:HGNC Symbol;Acc:HGNC:15876]"}, {"versioned_ensembl_gene_id":"ENSG00000269194.1","gene_symbol":"AC006942.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49808933,"end":49809738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242735.1","gene_symbol":"RPSAP26","gene_name":"ribosomal protein SA pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36195]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729209","summary":null,"start":62146413,"end":62147153,"strand":1,"description":"ribosomal protein SA pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36195]"}, {"versioned_ensembl_gene_id":"ENSG00000276050.1","gene_symbol":"IGKV2OR2-10","gene_name":"immunoglobulin kappa variable 2/OR2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5806]","synonyms":"IGKV2/OR2-10","biotype":"IG_V_pseudogene","ncbi_id":"28855","summary":null,"start":97331533,"end":97331843,"strand":-1,"description":"immunoglobulin kappa variable 2/OR2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5806]"}, {"versioned_ensembl_gene_id":"ENSG00000236355.2","gene_symbol":"AL391415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38714051,"end":38715217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230696.1","gene_symbol":"AC011753.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":109594693,"end":109605698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167333.12","gene_symbol":"TRIM68","gene_name":"tripartite motif containing 68 [Source:HGNC Symbol;Acc:HGNC:21161]","synonyms":"SS-56,RNF137,FLJ10369","biotype":"protein_coding","ncbi_id":"55128","summary":"This gene encodes a member of the tripartite motif-containing protein family, whose members are characterized by a \"really interesting new gene\" (RING) finger domain, a zinc-binding B-box motif, and a coiled-coil region. Members of this family function as E3 ubiquitin ligases and are involved in a broad range of biological processes. This gene regulates the activation of nuclear receptors, such as androgen receptor, and has been implicated in development of prostate cancer cells, where its expression increases in response to a downregulation of microRNAs. In addition, this gene participates in viral defense regulation as a negative regulator of interferon-beta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":4598672,"end":4608259,"strand":-1,"description":"tripartite motif containing 68 [Source:HGNC Symbol;Acc:HGNC:21161]"}, {"versioned_ensembl_gene_id":"ENSG00000279304.1","gene_symbol":"AP003072.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93133855,"end":93134164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183780.12","gene_symbol":"SLC35F3","gene_name":"solute carrier family 35 member F3 [Source:HGNC Symbol;Acc:HGNC:23616]","synonyms":"FLJ37712","biotype":"protein_coding","ncbi_id":"148641","summary":null,"start":233904933,"end":234324516,"strand":1,"description":"solute carrier family 35 member F3 [Source:HGNC Symbol;Acc:HGNC:23616]"}, {"versioned_ensembl_gene_id":"ENSG00000232166.1","gene_symbol":"AL122008.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":234284972,"end":234285541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280366.1","gene_symbol":"AL161782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79975023,"end":79990064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226700.1","gene_symbol":"MTND4P25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42212]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873246","summary":null,"start":82814984,"end":82815516,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42212]"}, {"versioned_ensembl_gene_id":"ENSG00000128708.12","gene_symbol":"HAT1","gene_name":"histone acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4821]","synonyms":"KAT1","biotype":"protein_coding","ncbi_id":"8520","summary":"The protein encoded by this gene is a type B histone acetyltransferase (HAT) that is involved in the rapid acetylation of newly synthesized cytoplasmic histones, which are in turn imported into the nucleus for de novo deposition onto nascent DNA chains. Histone acetylation, particularly of histone H4, plays an important role in replication-dependent chromatin assembly. Specifically, this HAT can acetylate soluble but not nucleosomal histone H4 at lysines 5 and 12, and to a lesser degree, histone H2A at lysine 5. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jun 2009]","start":171922448,"end":171983682,"strand":1,"description":"histone acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4821]"}, {"versioned_ensembl_gene_id":"ENSG00000259671.1","gene_symbol":"MTCYBP23","gene_name":"mitochondrially encoded cytochrome b pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51980]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075131","summary":null,"start":58154960,"end":58156061,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51980]"}, {"versioned_ensembl_gene_id":"ENSG00000103254.9","gene_symbol":"FAM173A","gene_name":"family with sequence similarity 173 member A [Source:HGNC Symbol;Acc:HGNC:14152]","synonyms":"MGC2494,C16orf24","biotype":"protein_coding","ncbi_id":"65990","summary":null,"start":720581,"end":722601,"strand":1,"description":"family with sequence similarity 173 member A [Source:HGNC Symbol;Acc:HGNC:14152]"}, {"versioned_ensembl_gene_id":"ENSG00000276692.1","gene_symbol":"CR769767.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39873931,"end":39874390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241429.1","gene_symbol":"EEF1A1P25","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37898]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646612","summary":null,"start":138825063,"end":138826329,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37898]"}, {"versioned_ensembl_gene_id":"ENSG00000179397.17","gene_symbol":"CATSPERE","gene_name":"catsper channel auxiliary subunit epsilon [Source:HGNC Symbol;Acc:HGNC:28491]","synonyms":"C1orf101,MGC33370","biotype":"protein_coding","ncbi_id":"257044","summary":null,"start":244454377,"end":244641177,"strand":1,"description":"catsper channel auxiliary subunit epsilon [Source:HGNC Symbol;Acc:HGNC:28491]"}, {"versioned_ensembl_gene_id":"ENSG00000074696.12","gene_symbol":"HACD3","gene_name":"3-hydroxyacyl-CoA dehydratase 3 [Source:HGNC Symbol;Acc:HGNC:24175]","synonyms":"PTPLAD1,HSPC121,B-ind1","biotype":"protein_coding","ncbi_id":"51495","summary":null,"start":65530418,"end":65578352,"strand":1,"description":"3-hydroxyacyl-CoA dehydratase 3 [Source:HGNC Symbol;Acc:HGNC:24175]"}, {"versioned_ensembl_gene_id":"ENSG00000227735.1","gene_symbol":"CYCSP5","gene_name":"cytochrome c, somatic pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:24416]","synonyms":"HCP5","biotype":"processed_pseudogene","ncbi_id":"360158","summary":null,"start":244598391,"end":244598687,"strand":-1,"description":"cytochrome c, somatic pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:24416]"}, {"versioned_ensembl_gene_id":"ENSG00000100364.18","gene_symbol":"KIAA0930","gene_name":"KIAA0930 [Source:HGNC Symbol;Acc:HGNC:1314]","synonyms":"C22orf9,bK268H5.C22.1","biotype":"protein_coding","ncbi_id":"23313","summary":null,"start":45190338,"end":45240769,"strand":-1,"description":"KIAA0930 [Source:HGNC Symbol;Acc:HGNC:1314]"}, {"versioned_ensembl_gene_id":"ENSG00000255127.3","gene_symbol":"AP003171.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92914603,"end":92931322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282916.1","gene_symbol":"AP003171.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92914272,"end":92915604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259149.1","gene_symbol":"AL445074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42259731,"end":42268586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164418.19","gene_symbol":"GRIK2","gene_name":"glutamate ionotropic receptor kainate type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4580]","synonyms":"MRT6,GLUR6,GluK2","biotype":"protein_coding","ncbi_id":"2898","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. The subunit encoded by this gene is subject to RNA editing at multiple sites within the first and second transmembrane domains, which is thought to alter the structure and function of the receptor complex. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. Mutations in this gene have been associated with autosomal recessive cognitive disability. [provided by RefSeq, Jul 2008]","start":101398788,"end":102070083,"strand":1,"description":"glutamate ionotropic receptor kainate type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4580]"}, {"versioned_ensembl_gene_id":"ENSG00000184371.13","gene_symbol":"CSF1","gene_name":"colony stimulating factor 1 [Source:HGNC Symbol;Acc:HGNC:2432]","synonyms":"M-CSF,MGC31930,MCSF","biotype":"protein_coding","ncbi_id":"1435","summary":"The protein encoded by this gene is a cytokine that controls the production, differentiation, and function of macrophages. The active form of the protein is found extracellularly as a disulfide-linked homodimer, and is thought to be produced by proteolytic cleavage of membrane-bound precursors. The encoded protein may be involved in development of the placenta. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":109910242,"end":109930992,"strand":1,"description":"colony stimulating factor 1 [Source:HGNC Symbol;Acc:HGNC:2432]"}, {"versioned_ensembl_gene_id":"ENSG00000267943.1","gene_symbol":"AC010328.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53007512,"end":53013180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275751.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786398,"end":54798220,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000095002.13","gene_symbol":"MSH2","gene_name":"mutS homolog 2 [Source:HGNC Symbol;Acc:HGNC:7325]","synonyms":"HNPCC1,HNPCC,COCA1","biotype":"protein_coding","ncbi_id":"4436","summary":"This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":47402969,"end":47562311,"strand":1,"description":"mutS homolog 2 [Source:HGNC Symbol;Acc:HGNC:7325]"}, {"versioned_ensembl_gene_id":"ENSG00000143196.4","gene_symbol":"DPT","gene_name":"dermatopontin [Source:HGNC Symbol;Acc:HGNC:3011]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1805","summary":"Dermatopontin is an extracellular matrix protein with possible functions in cell-matrix interactions and matrix assembly. The protein is found in various tissues and many of its tyrosine residues are sulphated. Dermatopontin is postulated to modify the behavior of TGF-beta through interaction with decorin. [provided by RefSeq, Jul 2008]","start":168695459,"end":168729264,"strand":-1,"description":"dermatopontin [Source:HGNC Symbol;Acc:HGNC:3011]"}, {"versioned_ensembl_gene_id":"ENSG00000268996.3","gene_symbol":"MAN1B1-AS1","gene_name":"MAN1B1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48715]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289341","summary":null,"start":137084946,"end":137086817,"strand":-1,"description":"MAN1B1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48715]"}, {"versioned_ensembl_gene_id":"ENSG00000225447.1","gene_symbol":"RPS15AP10","gene_name":"ribosomal protein S15a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37001]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728963","summary":null,"start":45645816,"end":45646197,"strand":-1,"description":"ribosomal protein S15a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37001]"}, {"versioned_ensembl_gene_id":"ENSG00000234329.1","gene_symbol":"AL604028.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45651039,"end":45651826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235119.1","gene_symbol":"AL138895.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114396724,"end":114398503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185303.16","gene_symbol":"SFTPA2","gene_name":"surfactant protein A2 [Source:HGNC Symbol;Acc:HGNC:10799]","synonyms":"SP-A2,COLEC5","biotype":"protein_coding","ncbi_id":"729238","summary":"This gene is one of several genes encoding pulmonary-surfactant associated proteins (SFTPA) located on chromosome 10. Mutations in this gene and a highly similar gene located nearby, which affect the highly conserved carbohydrate recognition domain, are associated with idiopathic pulmonary fibrosis. The current version of the assembly displays only a single centromeric SFTPA gene pair rather than the two gene pairs shown in the previous assembly which were thought to have resulted from a duplication. [provided by RefSeq, Sep 2009]","start":79555852,"end":79560402,"strand":-1,"description":"surfactant protein A2 [Source:HGNC Symbol;Acc:HGNC:10799]"}, {"versioned_ensembl_gene_id":"ENSG00000273353.1","gene_symbol":"AL008718.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45178990,"end":45179310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216913.2","gene_symbol":"AL049693.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50897615,"end":50898225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274578.1","gene_symbol":"AC006249.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28146233,"end":28146703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253376.1","gene_symbol":"AC012103.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57889576,"end":57890809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257184.3","gene_symbol":"AC004080.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":27163535,"end":27180013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234655.3","gene_symbol":"OR7E155P","gene_name":"olfactory receptor family 7 subfamily E member 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:31310]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403297","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":41439834,"end":41440847,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 155 pseudogene [Source:HGNC Symbol;Acc:HGNC:31310]"}, {"versioned_ensembl_gene_id":"ENSG00000260911.2","gene_symbol":"AC135050.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31043150,"end":31049868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234996.4","gene_symbol":"AC098934.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":202861754,"end":202875241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137831.14","gene_symbol":"UACA","gene_name":"uveal autoantigen with coiled-coil domains and ankyrin repeats [Source:HGNC Symbol;Acc:HGNC:15947]","synonyms":"KIAA1561,FLJ10128","biotype":"protein_coding","ncbi_id":"55075","summary":"This gene encodes a protein that contains ankyrin repeats and coiled coil domains and likely plays a role in apoptosis. Studies in rodents have implicated the encoded protein in the stimulation of apoptosis and the regulation of mammary gland involution, in which the mammary gland returns to its pre-pregnant state. This protein has also been proposed to negatively regulate apoptosis based on experiments in human cell lines in which the protein was shown to interact with PRKC apoptosis WT1 regulator protein, also known as PAR-4, and inhibit translocation of the PAR-4 receptor. Autoantibodies to this protein have been identified in human patients with panuveitis and Graves' disease. Differential expression of this gene has been observed in various human cancers. [provided by RefSeq, May 2017]","start":70654554,"end":70763593,"strand":-1,"description":"uveal autoantigen with coiled-coil domains and ankyrin repeats [Source:HGNC Symbol;Acc:HGNC:15947]"}, {"versioned_ensembl_gene_id":"ENSG00000165233.17","gene_symbol":"CARD19","gene_name":"caspase recruitment domain family member 19 [Source:HGNC Symbol;Acc:HGNC:28148]","synonyms":"MGC11115,C9orf89,BinCARD,bA370F5.1","biotype":"protein_coding","ncbi_id":"84270","summary":null,"start":93096218,"end":93113283,"strand":1,"description":"caspase recruitment domain family member 19 [Source:HGNC Symbol;Acc:HGNC:28148]"}, {"versioned_ensembl_gene_id":"ENSG00000009844.15","gene_symbol":"VTA1","gene_name":"vesicle trafficking 1 [Source:HGNC Symbol;Acc:HGNC:20954]","synonyms":"My012,HSPC228,C6orf55","biotype":"protein_coding","ncbi_id":"51534","summary":"C6ORF55 encodes a protein involved in trafficking of the multivesicular body, an endosomal compartment involved in sorting membrane proteins for degradation in lysosomes (Ward et al., 2005 [PubMed 15644320]).[supplied by OMIM, Mar 2008]","start":142147162,"end":142224689,"strand":1,"description":"vesicle trafficking 1 [Source:HGNC Symbol;Acc:HGNC:20954]"}, {"versioned_ensembl_gene_id":"ENSG00000228403.1","gene_symbol":"AC035139.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48878022,"end":48878649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263355.1","gene_symbol":"AKR1B10P2","gene_name":"aldo-keto reductase family 1 member B10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45063]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643582","summary":null,"start":68455951,"end":68456877,"strand":1,"description":"aldo-keto reductase family 1 member B10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45063]"}, {"versioned_ensembl_gene_id":"ENSG00000228754.1","gene_symbol":"RPL13AP19","gene_name":"ribosomal protein L13a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:35855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132924","summary":null,"start":48745545,"end":48746128,"strand":-1,"description":"ribosomal protein L13a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:35855]"}, {"versioned_ensembl_gene_id":"ENSG00000265425.1","gene_symbol":"AC005909.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68427030,"end":68436918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217555.12","gene_symbol":"CKLF","gene_name":"chemokine like factor [Source:HGNC Symbol;Acc:HGNC:13253]","synonyms":"UCK-1,HSPC224,CKLF4,CKLF3,CKLF1,C32","biotype":"protein_coding","ncbi_id":"51192","summary":"The product of this gene is a cytokine. Cytokines are small proteins that have an essential role in the immune and inflammatory responses. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. The protein encoded by this gene is a potent chemoattractant for neutrophils, monocytes and lymphocytes. It also can stimulate the proliferation of skeletal muscle cells. This protein may play important roles in inflammation and in the regeneration of skeletal muscle. Alternatively spliced transcript variants encoding different isoforms have been identified. Naturally occurring read-through transcription occurs between this locus and the neighboring locus CMTM1 (CKLF-like MARVEL transmembrane domain containing 1).[provided by RefSeq, Feb 2011]","start":66552563,"end":66566251,"strand":1,"description":"chemokine like factor [Source:HGNC Symbol;Acc:HGNC:13253]"}, {"versioned_ensembl_gene_id":"ENSG00000280023.1","gene_symbol":"AD000813.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36070239,"end":36071070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075702.16","gene_symbol":"WDR62","gene_name":"WD repeat domain 62 [Source:HGNC Symbol;Acc:HGNC:24502]","synonyms":"MCPH2,FLJ33298,DKFZP434J046,C19orf14","biotype":"protein_coding","ncbi_id":"284403","summary":"This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]","start":36054881,"end":36105106,"strand":1,"description":"WD repeat domain 62 [Source:HGNC Symbol;Acc:HGNC:24502]"}, {"versioned_ensembl_gene_id":"ENSG00000231746.1","gene_symbol":"BX119924.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28862129,"end":28862760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140694.16","gene_symbol":"PARN","gene_name":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]","synonyms":"DAN","biotype":"protein_coding","ncbi_id":"5073","summary":"The protein encoded by this gene is a 3'-exoribonuclease, with similarity to the RNase D family of 3'-exonucleases. It prefers poly(A) as the substrate, hence, efficiently degrades poly(A) tails of mRNAs. Exonucleolytic degradation of the poly(A) tail is often the first step in the decay of eukaryotic mRNAs. This protein is also involved in silencing of certain maternal mRNAs during oocyte maturation and early embryonic development, as well as in nonsense-mediated decay (NMD) of mRNAs that contain premature stop codons. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":14435701,"end":14632728,"strand":-1,"description":"poly(A)-specific ribonuclease [Source:HGNC Symbol;Acc:HGNC:8609]"}, {"versioned_ensembl_gene_id":"ENSG00000277425.1","gene_symbol":"AL121890.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5066082,"end":5068154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142156.14","gene_symbol":"COL6A1","gene_name":"collagen type VI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2211]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1291","summary":"The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy. [provided by RefSeq, Jul 2008]","start":45981737,"end":46005050,"strand":1,"description":"collagen type VI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2211]"}, {"versioned_ensembl_gene_id":"ENSG00000213180.4","gene_symbol":"RPL36AP48","gene_name":"ribosomal protein L36a pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36721]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646175","summary":null,"start":67224728,"end":67225041,"strand":1,"description":"ribosomal protein L36a pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36721]"}, {"versioned_ensembl_gene_id":"ENSG00000184470.20","gene_symbol":"TXNRD2","gene_name":"thioredoxin reductase 2 [Source:HGNC Symbol;Acc:HGNC:18155]","synonyms":"TRXR2,TR3,TR","biotype":"protein_coding","ncbi_id":"10587","summary":"The protein encoded by this gene belongs to the pyridine nucleotide-disulfide oxidoreductase family, and is a member of the thioredoxin (Trx) system. Three thioredoxin reductase (TrxR) isozymes are found in mammals. TrxRs are selenocysteine-containing flavoenzymes, which reduce thioredoxins, as well as other substrates, and play a key role in redox homoeostasis. This gene encodes a mitochondrial form important for scavenging reactive oxygen species in mitochondria. It functions as a homodimer containing FAD, and selenocysteine (Sec) at the active site. Sec is encoded by UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Alternatively spliced transcript variants encoding different isoforms, including a few localized in the cytosol and some lacking the C-terminal Sec residue, have been found for this gene. [provided by RefSeq, Jun 2017]","start":19875517,"end":19941992,"strand":-1,"description":"thioredoxin reductase 2 [Source:HGNC Symbol;Acc:HGNC:18155]"}, {"versioned_ensembl_gene_id":"ENSG00000181358.3","gene_symbol":"CTAGE10P","gene_name":"CTAGE family member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:37288]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"220429","summary":null,"start":49890591,"end":49892998,"strand":1,"description":"CTAGE family member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:37288]"}, {"versioned_ensembl_gene_id":"ENSG00000108878.4","gene_symbol":"CACNG1","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:1405]","synonyms":"CACNLG","biotype":"protein_coding","ncbi_id":"786","summary":"Voltage-dependent calcium channels are composed of five subunits. The protein encoded by this gene represents one of these subunits, gamma, and is one of two known gamma subunit proteins. This particular gamma subunit is part of skeletal muscle 1,4-dihydropyridine-sensitive calcium channels and is an integral membrane protein that plays a role in excitation-contraction coupling. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members that function as transmembrane AMPA receptor regulatory proteins (TARPs). [provided by RefSeq, Dec 2010]","start":67044590,"end":67056797,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:1405]"}, {"versioned_ensembl_gene_id":"ENSG00000168811.6","gene_symbol":"IL12A","gene_name":"interleukin 12A [Source:HGNC Symbol;Acc:HGNC:5969]","synonyms":"p35,NKSF1,NFSK,IL-12A,CLMF","biotype":"protein_coding","ncbi_id":"3592","summary":"This gene encodes a subunit of a cytokine that acts on T and natural killer cells, and has a broad array of biological activities. The cytokine is a disulfide-linked heterodimer composed of the 35-kD subunit encoded by this gene, and a 40-kD subunit that is a member of the cytokine receptor family. This cytokine is required for the T-cell-independent induction of interferon (IFN)-gamma, and is important for the differentiation of both Th1 and Th2 cells. The responses of lymphocytes to this cytokine are mediated by the activator of transcription protein STAT4. Nitric oxide synthase 2A (NOS2A/NOS2) is found to be required for the signaling process of this cytokine in innate immunity. [provided by RefSeq, Jul 2008]","start":159988750,"end":159996019,"strand":1,"description":"interleukin 12A [Source:HGNC Symbol;Acc:HGNC:5969]"}, {"versioned_ensembl_gene_id":"ENSG00000269353.1","gene_symbol":"AC092071.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40946347,"end":40947450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075429.8","gene_symbol":"CACNG5","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 5 [Source:HGNC Symbol;Acc:HGNC:1409]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27091","summary":"The protein encoded by this gene is a type II transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type I TARP and a calcium channel gamma subunit. This gene is a susceptibility locus for schizophrenia and bipolar disorder. [provided by RefSeq, Dec 2010]","start":66835117,"end":66885486,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 5 [Source:HGNC Symbol;Acc:HGNC:1409]"}, {"versioned_ensembl_gene_id":"ENSG00000271243.1","gene_symbol":"AC016727.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61575774,"end":61576394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279593.1","gene_symbol":"AL132642.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93895762,"end":93897759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256353.1","gene_symbol":"AC087258.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23108458,"end":23108493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244879.6","gene_symbol":"GABPB1-AS1","gene_name":"GABPB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44157]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129387","summary":null,"start":50354959,"end":50372202,"strand":1,"description":"GABPB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44157]"}, {"versioned_ensembl_gene_id":"ENSG00000179454.13","gene_symbol":"KLHL28","gene_name":"kelch like family member 28 [Source:HGNC Symbol;Acc:HGNC:19741]","synonyms":"FLJ20081,BTBD5","biotype":"protein_coding","ncbi_id":"54813","summary":null,"start":44924319,"end":45042322,"strand":-1,"description":"kelch like family member 28 [Source:HGNC Symbol;Acc:HGNC:19741]"}, {"versioned_ensembl_gene_id":"ENSG00000263466.1","gene_symbol":"AC006441.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38903704,"end":38904600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274248.1","gene_symbol":"AJ011932.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45974489,"end":45974953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249012.2","gene_symbol":"AC104819.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151259503,"end":151262849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271974.1","gene_symbol":"AC103810.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64905883,"end":64906018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272220.1","gene_symbol":"AC103810.8","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64892728,"end":64892845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275138.1","gene_symbol":"AL357080.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141019788,"end":141020026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254254.5","gene_symbol":"AC012349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56445807,"end":56552067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249706.1","gene_symbol":"AC105384.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53899871,"end":53916835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112249.13","gene_symbol":"ASCC3","gene_name":"activating signal cointegrator 1 complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:18697]","synonyms":"RNAH,HELIC1,dJ467N11.1,dJ121G13.4,ASC1p200","biotype":"protein_coding","ncbi_id":"10973","summary":"This gene encodes a protein that belongs to a family of helicases that are involved in the ATP-dependent unwinding of nucleic acid duplexes. The encoded protein is the largest subunit of the activating signal cointegrator 1 complex that is involved in DNA repair and resistance to alkylation damage. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":100508194,"end":100881372,"strand":-1,"description":"activating signal cointegrator 1 complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:18697]"}, {"versioned_ensembl_gene_id":"ENSG00000281333.1","gene_symbol":"AC024941.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88580531,"end":88598218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145723.16","gene_symbol":"GIN1","gene_name":"gypsy retrotransposon integrase 1 [Source:HGNC Symbol;Acc:HGNC:25959]","synonyms":"TGIN1,GIN-1,FLJ20125,ZH2C2","biotype":"protein_coding","ncbi_id":"54826","summary":null,"start":103086000,"end":103120151,"strand":-1,"description":"gypsy retrotransposon integrase 1 [Source:HGNC Symbol;Acc:HGNC:25959]"}, {"versioned_ensembl_gene_id":"ENSG00000148843.13","gene_symbol":"PDCD11","gene_name":"programmed cell death 11 [Source:HGNC Symbol;Acc:HGNC:13408]","synonyms":"RRP5,KIAA0185,ALG-4","biotype":"protein_coding","ncbi_id":"22984","summary":"PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation of 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008]","start":103396648,"end":103446292,"strand":1,"description":"programmed cell death 11 [Source:HGNC Symbol;Acc:HGNC:13408]"}, {"versioned_ensembl_gene_id":"ENSG00000124226.10","gene_symbol":"RNF114","gene_name":"ring finger protein 114 [Source:HGNC Symbol;Acc:HGNC:13094]","synonyms":"ZNF313,PSORS12","biotype":"protein_coding","ncbi_id":"55905","summary":null,"start":49936336,"end":49953892,"strand":1,"description":"ring finger protein 114 [Source:HGNC Symbol;Acc:HGNC:13094]"}, {"versioned_ensembl_gene_id":"ENSG00000256193.5","gene_symbol":"LINC00507","gene_name":"long intergenic non-protein coding RNA 507 [Source:HGNC Symbol;Acc:HGNC:43558]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100862680","summary":null,"start":127915372,"end":127951552,"strand":1,"description":"long intergenic non-protein coding RNA 507 [Source:HGNC Symbol;Acc:HGNC:43558]"}, {"versioned_ensembl_gene_id":"ENSG00000256597.2","gene_symbol":"LINC02393","gene_name":"long intergenic non-protein coding RNA 2393 [Source:HGNC Symbol;Acc:HGNC:53320]","synonyms":"FLJ37505","biotype":"lincRNA","ncbi_id":"400087","summary":null,"start":127881617,"end":127898639,"strand":1,"description":"long intergenic non-protein coding RNA 2393 [Source:HGNC Symbol;Acc:HGNC:53320]"}, {"versioned_ensembl_gene_id":"ENSG00000264685.1","gene_symbol":"PRPF19P1","gene_name":"PRPF19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23182]","synonyms":"PRPF19P,PRP19P,HsT1682","biotype":"processed_pseudogene","ncbi_id":"100422496","summary":null,"start":66068750,"end":66069647,"strand":-1,"description":"PRPF19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23182]"}, {"versioned_ensembl_gene_id":"ENSG00000266820.1","gene_symbol":"KPNA2P3","gene_name":"karyopherin subunit alpha 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52870]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"109286552","summary":null,"start":64749918,"end":64758603,"strand":-1,"description":"karyopherin subunit alpha 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52870]"}, {"versioned_ensembl_gene_id":"ENSG00000166152.3","gene_symbol":"C16orf78","gene_name":"chromosome 16 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:28479]","synonyms":"MGC33367","biotype":"protein_coding","ncbi_id":"123970","summary":null,"start":49373823,"end":49399431,"strand":1,"description":"chromosome 16 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:28479]"}, {"versioned_ensembl_gene_id":"ENSG00000253170.1","gene_symbol":"AC108515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97120701,"end":97135059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263647.1","gene_symbol":"BPTFP1","gene_name":"bromodomain PHD finger transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52869]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109286551","summary":null,"start":64761912,"end":64762710,"strand":-1,"description":"bromodomain PHD finger transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52869]"}, {"versioned_ensembl_gene_id":"ENSG00000268278.1","gene_symbol":"AC123912.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21637974,"end":21656300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232872.2","gene_symbol":"CTAGE3P","gene_name":"CTAGE family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:24348]","synonyms":"CTAGE3,cTAGE-3","biotype":"processed_pseudogene","ncbi_id":"220112","summary":null,"start":51908218,"end":51910621,"strand":-1,"description":"CTAGE family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:24348]"}, {"versioned_ensembl_gene_id":"ENSG00000143147.14","gene_symbol":"GPR161","gene_name":"G protein-coupled receptor 161 [Source:HGNC Symbol;Acc:HGNC:23694]","synonyms":"RE2","biotype":"protein_coding","ncbi_id":"23432","summary":"The protein encoded by this gene is an orphan G protein-coupled receptor whose ligand is unknown. This gene is overexpressed in triple-negative breast cancer, and disruption of this gene slows the proliferation of basal breast cancer cells. Therefore, this gene is a potential drug target for triple-negative breast cancer. [provided by RefSeq, Mar 2017]","start":168079543,"end":168137667,"strand":-1,"description":"G protein-coupled receptor 161 [Source:HGNC Symbol;Acc:HGNC:23694]"}, {"versioned_ensembl_gene_id":"ENSG00000266931.1","gene_symbol":"AC125232.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87055658,"end":87055800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211887.2","gene_symbol":"TRAJ2","gene_name":"T-cell receptor alpha joining 2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12048]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28753","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22544071,"end":22544136,"strand":1,"description":"T-cell receptor alpha joining 2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12048]"}, {"versioned_ensembl_gene_id":"ENSG00000237248.4","gene_symbol":"LINC00987","gene_name":"long intergenic non-protein coding RNA 987 [Source:HGNC Symbol;Acc:HGNC:48911]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100499405","summary":null,"start":9240003,"end":9243052,"strand":1,"description":"long intergenic non-protein coding RNA 987 [Source:HGNC Symbol;Acc:HGNC:48911]"}, {"versioned_ensembl_gene_id":"ENSG00000063176.15","gene_symbol":"SPHK2","gene_name":"sphingosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:18859]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56848","summary":"This gene encodes one of two sphingosine kinase isozymes that catalyze the phosphorylation of sphingosine into sphingosine 1-phosphate. Sphingosine 1-phosphate mediates many cellular processes including migration, proliferation and apoptosis, and also plays a role in several types of cancer by promoting angiogenesis and tumorigenesis. The encoded protein may play a role in breast cancer proliferation and chemoresistance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":48619291,"end":48630717,"strand":1,"description":"sphingosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:18859]"}, {"versioned_ensembl_gene_id":"ENSG00000256427.1","gene_symbol":"AC010175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9246497,"end":9257960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226248.6","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31712749,"end":31721936,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000221813.4","gene_symbol":"OR6B1","gene_name":"olfactory receptor family 6 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8354]","synonyms":"OR7-3","biotype":"protein_coding","ncbi_id":"135946","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144000320,"end":144008793,"strand":1,"description":"olfactory receptor family 6 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:8354]"}, {"versioned_ensembl_gene_id":"ENSG00000186166.8","gene_symbol":"CCDC84","gene_name":"coiled-coil domain containing 84 [Source:HGNC Symbol;Acc:HGNC:30460]","synonyms":"DLNB14","biotype":"protein_coding","ncbi_id":"338657","summary":"This gene encodes a protein thought to contain a coiled coil motif. No function has been determined for the encoded protein. A pseudogene of this gene is located on chromosome 20. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":118998142,"end":119015791,"strand":1,"description":"coiled-coil domain containing 84 [Source:HGNC Symbol;Acc:HGNC:30460]"}, {"versioned_ensembl_gene_id":"ENSG00000249352.4","gene_symbol":"LINC02198","gene_name":"long intergenic non-protein coding RNA 2198 [Source:HGNC Symbol;Acc:HGNC:53064]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928885","summary":null,"start":68970692,"end":69030165,"strand":-1,"description":"long intergenic non-protein coding RNA 2198 [Source:HGNC Symbol;Acc:HGNC:53064]"}, {"versioned_ensembl_gene_id":"ENSG00000271779.1","gene_symbol":"AC009994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64572829,"end":64573081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250066.1","gene_symbol":"AC093248.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68963246,"end":68967845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235606.3","gene_symbol":"AK4P6","gene_name":"adenylate kinase 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649288","summary":null,"start":151027090,"end":151027617,"strand":1,"description":"adenylate kinase 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39069]"}, {"versioned_ensembl_gene_id":"ENSG00000235313.1","gene_symbol":"HM13-IT1","gene_name":"HM13 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41424]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480432","summary":null,"start":31563166,"end":31564076,"strand":1,"description":"HM13 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41424]"}, {"versioned_ensembl_gene_id":"ENSG00000229601.1","gene_symbol":"AL590762.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71413834,"end":71414086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228939.1","gene_symbol":"AKT3-IT1","gene_name":"AKT3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41304]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874263","summary":null,"start":243793205,"end":243794400,"strand":-1,"description":"AKT3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41304]"}, {"versioned_ensembl_gene_id":"ENSG00000143368.9","gene_symbol":"SF3B4","gene_name":"splicing factor 3b subunit 4 [Source:HGNC Symbol;Acc:HGNC:10771]","synonyms":"SF3b49,SAP49,Hsh49","biotype":"protein_coding","ncbi_id":"10262","summary":"This gene encodes one of four subunits of the splicing factor 3B. The protein encoded by this gene cross-links to a region in the pre-mRNA immediately upstream of the branchpoint sequence in pre-mRNA in the prespliceosomal complex A. It also may be involved in the assembly of the B, C and E spliceosomal complexes. In addition to RNA-binding activity, this protein interacts directly and highly specifically with subunit 2 of the splicing factor 3B. This protein contains two N-terminal RNA-recognition motifs (RRMs), consistent with the observation that it binds directly to pre-mRNA. [provided by RefSeq, Jul 2008]","start":149923317,"end":149928344,"strand":-1,"description":"splicing factor 3b subunit 4 [Source:HGNC Symbol;Acc:HGNC:10771]"}, {"versioned_ensembl_gene_id":"ENSG00000258850.1","gene_symbol":"AL450442.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42412573,"end":42528888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224187.1","gene_symbol":"LINC01991","gene_name":"long intergenic non-protein coding RNA 1991 [Source:HGNC Symbol;Acc:HGNC:52823]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374266","summary":null,"start":187958775,"end":187976407,"strand":-1,"description":"long intergenic non-protein coding RNA 1991 [Source:HGNC Symbol;Acc:HGNC:52823]"}, {"versioned_ensembl_gene_id":"ENSG00000232843.2","gene_symbol":"SNX18P2","gene_name":"sorting nexin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39610]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642952","summary":null,"start":92893698,"end":92894505,"strand":-1,"description":"sorting nexin 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39610]"}, {"versioned_ensembl_gene_id":"ENSG00000211851.1","gene_symbol":"TRAJ38","gene_name":"T-cell receptor alpha joining 38 [Source:HGNC Symbol;Acc:HGNC:12068]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28717","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22502231,"end":22502292,"strand":1,"description":"T-cell receptor alpha joining 38 [Source:HGNC Symbol;Acc:HGNC:12068]"}, {"versioned_ensembl_gene_id":"ENSG00000269553.1","gene_symbol":"U62631.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35330843,"end":35331920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249311.4","gene_symbol":"TERF1P3","gene_name":"telomeric repeat binding factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38499]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646316","summary":null,"start":136355110,"end":136356336,"strand":-1,"description":"telomeric repeat binding factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38499]"}, {"versioned_ensembl_gene_id":"ENSG00000222042.1","gene_symbol":"AP001341.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25169431,"end":25333825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213885.3","gene_symbol":"RPL13AP7","gene_name":"ribosomal protein L13a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23755]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284821","summary":null,"start":25361821,"end":25362431,"strand":1,"description":"ribosomal protein L13a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23755]"}, {"versioned_ensembl_gene_id":"ENSG00000234696.1","gene_symbol":"GPR50-AS1","gene_name":"GPR50 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40259]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128688","summary":null,"start":151175192,"end":151177836,"strand":-1,"description":"GPR50 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40259]"}, {"versioned_ensembl_gene_id":"ENSG00000187474.4","gene_symbol":"FPR3","gene_name":"formyl peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:3828]","synonyms":"FPRH1,FMLPY,RMLP-R-I,FPRL2","biotype":"protein_coding","ncbi_id":"2359","summary":null,"start":51795163,"end":51826189,"strand":1,"description":"formyl peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:3828]"}, {"versioned_ensembl_gene_id":"ENSG00000257103.8","gene_symbol":"LSM14A","gene_name":"LSM14A, mRNA processing body assembly factor [Source:HGNC Symbol;Acc:HGNC:24489]","synonyms":"RAP55A,RAP55,FAM61A,DKFZP434D1335,C19orf13","biotype":"protein_coding","ncbi_id":"26065","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Mar 2008]","start":34172504,"end":34229515,"strand":1,"description":"LSM14A, mRNA processing body assembly factor [Source:HGNC Symbol;Acc:HGNC:24489]"}, {"versioned_ensembl_gene_id":"ENSG00000166507.17","gene_symbol":"NDST2","gene_name":"N-deacetylase and N-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:7681]","synonyms":"NST2,HSST2","biotype":"protein_coding","ncbi_id":"8509","summary":"This gene encodes a member of the N-deacetylase/N-sulfotransferase subfamily of the sulfotransferase 1 proteins. The encoded enzyme has dual functions in processing glucosamine and heparin polymers, including N-deacetylation and N-sulfation. The encoded protein may be localized to the Golgi. [provided by RefSeq, Feb 2009]","start":73801911,"end":73811798,"strand":-1,"description":"N-deacetylase and N-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:7681]"}, {"versioned_ensembl_gene_id":"ENSG00000280238.1","gene_symbol":"AC022400.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73791218,"end":73791490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203909.3","gene_symbol":"DPPA5","gene_name":"developmental pluripotency associated 5 [Source:HGNC Symbol;Acc:HGNC:19201]","synonyms":"Esg1","biotype":"protein_coding","ncbi_id":"340168","summary":"This gene encodes a protein that may function in the control of cell pluripotency and early embryogenesis. Expression of this gene is a specific marker for pluripotent stem cells. Pseudogenes of this gene are located on the short arm of chromosome 10 and the long arm of chromosomes 14 and 19. [provided by RefSeq, Dec 2010]","start":73353062,"end":73354295,"strand":-1,"description":"developmental pluripotency associated 5 [Source:HGNC Symbol;Acc:HGNC:19201]"}, {"versioned_ensembl_gene_id":"ENSG00000224563.1","gene_symbol":"LPP-AS1","gene_name":"LPP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40346]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873917","summary":null,"start":188562238,"end":188568666,"strand":-1,"description":"LPP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40346]"}, {"versioned_ensembl_gene_id":"ENSG00000248528.1","gene_symbol":"LINC02058","gene_name":"long intergenic non-protein coding RNA 2058 [Source:HGNC Symbol;Acc:HGNC:52901]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984117","summary":null,"start":92907180,"end":92939591,"strand":-1,"description":"long intergenic non-protein coding RNA 2058 [Source:HGNC Symbol;Acc:HGNC:52901]"}, {"versioned_ensembl_gene_id":"ENSG00000266402.3","gene_symbol":"SNHG25","gene_name":"small nucleolar RNA host gene 25 [Source:HGNC Symbol;Acc:HGNC:51534]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376843","summary":null,"start":64145970,"end":64146476,"strand":1,"description":"small nucleolar RNA host gene 25 [Source:HGNC Symbol;Acc:HGNC:51534]"}, {"versioned_ensembl_gene_id":"ENSG00000211846.1","gene_symbol":"TRAJ43","gene_name":"T-cell receptor alpha joining 43 [Source:HGNC Symbol;Acc:HGNC:12074]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28712","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22495913,"end":22495966,"strand":1,"description":"T-cell receptor alpha joining 43 [Source:HGNC Symbol;Acc:HGNC:12074]"}, {"versioned_ensembl_gene_id":"ENSG00000270372.1","gene_symbol":"AL162413.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10948372,"end":10948481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249679.1","gene_symbol":"AC106897.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185471516,"end":185472263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116874.11","gene_symbol":"WARS2","gene_name":"tryptophanyl tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12730]","synonyms":"TrpRS","biotype":"protein_coding","ncbi_id":"10352","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Two forms of tryptophanyl-tRNA synthetase exist, a cytoplasmic form, named WARS, and a mitochondrial form, named WARS2. This gene encodes the mitochondrial tryptophanyl-tRNA synthetase. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":119031216,"end":119140671,"strand":-1,"description":"tryptophanyl tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:12730]"}, {"versioned_ensembl_gene_id":"ENSG00000226087.1","gene_symbol":"AC073283.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47225794,"end":47239225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231365.5","gene_symbol":"AL359915.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119140396,"end":119275973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211842.1","gene_symbol":"TRAJ47","gene_name":"T-cell receptor alpha joining 47 [Source:HGNC Symbol;Acc:HGNC:12078]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28708","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22492851,"end":22492907,"strand":1,"description":"T-cell receptor alpha joining 47 [Source:HGNC Symbol;Acc:HGNC:12078]"}, {"versioned_ensembl_gene_id":"ENSG00000204031.3","gene_symbol":"LCN1P2","gene_name":"lipocalin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23680]","synonyms":"LCN1L2,bA244N20.11","biotype":"unprocessed_pseudogene","ncbi_id":"653163","summary":null,"start":133317794,"end":133318469,"strand":1,"description":"lipocalin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23680]"}, {"versioned_ensembl_gene_id":"ENSG00000282618.1","gene_symbol":"TRBV10-1","gene_name":"T-cell receptor beta variable 10-1(gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12177]","synonyms":"TCRBV12S2,TCRBV10S1,TRBV101,TCRBV12S2A1T","biotype":"TR_V_gene","ncbi_id":"28585","summary":null,"start":142421573,"end":142422090,"strand":1,"description":"T-cell receptor beta variable 10-1(gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12177]"}, {"versioned_ensembl_gene_id":"ENSG00000236804.1","gene_symbol":"RPS3AP12","gene_name":"ribosomal protein S3a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35527]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270905","summary":null,"start":119126539,"end":119127291,"strand":-1,"description":"ribosomal protein S3a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35527]"}, {"versioned_ensembl_gene_id":"ENSG00000260096.1","gene_symbol":"DNM1P33","gene_name":"dynamin 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35180]","synonyms":"DNM1DN7@,DNM1DN7-2","biotype":"unprocessed_pseudogene","ncbi_id":"554175","summary":null,"start":74062780,"end":74063785,"strand":1,"description":"dynamin 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35180]"}, {"versioned_ensembl_gene_id":"ENSG00000146007.10","gene_symbol":"ZMAT2","gene_name":"zinc finger matrin-type 2 [Source:HGNC Symbol;Acc:HGNC:26433]","synonyms":"Snu23,hSNU23,FLJ31121","biotype":"protein_coding","ncbi_id":"153527","summary":null,"start":140698680,"end":140706676,"strand":1,"description":"zinc finger matrin-type 2 [Source:HGNC Symbol;Acc:HGNC:26433]"}, {"versioned_ensembl_gene_id":"ENSG00000284612.1","gene_symbol":"AL591543.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38650215,"end":38662717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099284.13","gene_symbol":"H2AFY2","gene_name":"H2A histone family member Y2 [Source:HGNC Symbol;Acc:HGNC:14453]","synonyms":"macroH2A2","biotype":"protein_coding","ncbi_id":"55506","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. It replaces conventional H2A histones in a subset of nucleosomes where it represses transcription and may participate in stable X chromosome inactivation. [provided by RefSeq, Oct 2015]","start":70052796,"end":70112280,"strand":1,"description":"H2A histone family member Y2 [Source:HGNC Symbol;Acc:HGNC:14453]"}, {"versioned_ensembl_gene_id":"ENSG00000180172.7","gene_symbol":"RPS12P23","gene_name":"ribosomal protein S12 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35573]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338870","summary":null,"start":21094315,"end":21094714,"strand":-1,"description":"ribosomal protein S12 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35573]"}, {"versioned_ensembl_gene_id":"ENSG00000258902.1","gene_symbol":"AL049775.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85362457,"end":85516934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259107.1","gene_symbol":"LINC00911","gene_name":"long intergenic non-protein coding RNA 911 [Source:HGNC Symbol;Acc:HGNC:48596]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996280","summary":null,"start":85393879,"end":85420074,"strand":1,"description":"long intergenic non-protein coding RNA 911 [Source:HGNC Symbol;Acc:HGNC:48596]"}, {"versioned_ensembl_gene_id":"ENSG00000163138.18","gene_symbol":"PACRGL","gene_name":"parkin coregulated like [Source:HGNC Symbol;Acc:HGNC:28442]","synonyms":"MGC29898,C4orf28","biotype":"protein_coding","ncbi_id":"133015","summary":null,"start":20696282,"end":20752907,"strand":1,"description":"parkin coregulated like [Source:HGNC Symbol;Acc:HGNC:28442]"}, {"versioned_ensembl_gene_id":"ENSG00000171561.4","gene_symbol":"OR2AT4","gene_name":"olfactory receptor family 2 subfamily AT member 4 [Source:HGNC Symbol;Acc:HGNC:19620]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341152","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":75081753,"end":75096876,"strand":-1,"description":"olfactory receptor family 2 subfamily AT member 4 [Source:HGNC Symbol;Acc:HGNC:19620]"}, {"versioned_ensembl_gene_id":"ENSG00000114107.8","gene_symbol":"CEP70","gene_name":"centrosomal protein 70 [Source:HGNC Symbol;Acc:HGNC:29972]","synonyms":"FLJ13036,BITE","biotype":"protein_coding","ncbi_id":"80321","summary":null,"start":138494344,"end":138594538,"strand":-1,"description":"centrosomal protein 70 [Source:HGNC Symbol;Acc:HGNC:29972]"}, {"versioned_ensembl_gene_id":"ENSG00000213669.2","gene_symbol":"AL137074.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92676943,"end":92677407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204776.6","gene_symbol":"IGKV1OR-3","gene_name":"immunoglobulin kappa variable 1/OR-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5762]","synonyms":"IGKVPZ3,IGKV1/OR-3","biotype":"IG_V_pseudogene","ncbi_id":"644731","summary":null,"start":65770955,"end":65771434,"strand":1,"description":"immunoglobulin kappa variable 1/OR-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5762]"}, {"versioned_ensembl_gene_id":"ENSG00000271762.1","gene_symbol":"AC123595.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91313057,"end":91314402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131482.9","gene_symbol":"G6PC","gene_name":"glucose-6-phosphatase catalytic subunit [Source:HGNC Symbol;Acc:HGNC:4056]","synonyms":"GSD1a,G6PT","biotype":"protein_coding","ncbi_id":"2538","summary":"Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]","start":42900797,"end":42913369,"strand":1,"description":"glucose-6-phosphatase catalytic subunit [Source:HGNC Symbol;Acc:HGNC:4056]"}, {"versioned_ensembl_gene_id":"ENSG00000234292.3","gene_symbol":"AC123595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91280097,"end":91281142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258923.2","gene_symbol":"MTND5P35","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:51954]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075119","summary":null,"start":84173791,"end":84175510,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:51954]"}, {"versioned_ensembl_gene_id":"ENSG00000258762.1","gene_symbol":"MTND4P33","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:51947]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075253","summary":null,"start":84172841,"end":84173606,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:51947]"}, {"versioned_ensembl_gene_id":"ENSG00000261857.6","gene_symbol":"MIA","gene_name":"melanoma inhibitory activity [Source:HGNC Symbol;Acc:HGNC:7076]","synonyms":"CD-RAP","biotype":"protein_coding","ncbi_id":"8190","summary":null,"start":40771648,"end":40777490,"strand":1,"description":"melanoma inhibitory activity [Source:HGNC Symbol;Acc:HGNC:7076]"}, {"versioned_ensembl_gene_id":"ENSG00000260688.1","gene_symbol":"AC026470.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48470953,"end":48471133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197601.12","gene_symbol":"FAR1","gene_name":"fatty acyl-CoA reductase 1 [Source:HGNC Symbol;Acc:HGNC:26222]","synonyms":"FLJ22728,SDR10E1,MLSTD2","biotype":"protein_coding","ncbi_id":"84188","summary":"The protein encoded by this gene is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jan 2015]","start":13668670,"end":13732346,"strand":1,"description":"fatty acyl-CoA reductase 1 [Source:HGNC Symbol;Acc:HGNC:26222]"}, {"versioned_ensembl_gene_id":"ENSG00000231227.1","gene_symbol":"AC006450.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":124010530,"end":124011114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271172.1","gene_symbol":"AC104662.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25220403,"end":25220913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227090.1","gene_symbol":"AP000402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24886676,"end":24902756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250688.1","gene_symbol":"TRAJ55","gene_name":"T-cell receptor alpha joining 55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12087]","synonyms":null,"biotype":"TR_J_pseudogene","ncbi_id":"28700","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22481697,"end":22481753,"strand":1,"description":"T-cell receptor alpha joining 55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12087]"}, {"versioned_ensembl_gene_id":"ENSG00000276633.1","gene_symbol":"AJ011931.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45870854,"end":45873345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249700.8","gene_symbol":"SRD5A3-AS1","gene_name":"SRD5A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44138]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506462","summary":null,"start":55363971,"end":55395847,"strand":-1,"description":"SRD5A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44138]"}, {"versioned_ensembl_gene_id":"ENSG00000213706.2","gene_symbol":"AL590762.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71352418,"end":71352988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149646.12","gene_symbol":"CNBD2","gene_name":"cyclic nucleotide binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16145]","synonyms":"dJ954P9.1,CNMPD1,C20orf152","biotype":"protein_coding","ncbi_id":"140894","summary":null,"start":35954564,"end":36030700,"strand":1,"description":"cyclic nucleotide binding domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16145]"}, {"versioned_ensembl_gene_id":"ENSG00000274553.1","gene_symbol":"AC138035.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181329049,"end":181331839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231858.5","gene_symbol":"AC067945.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":191021526,"end":191032314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214338.10","gene_symbol":"SOGA3","gene_name":"SOGA family member 3 [Source:HGNC Symbol;Acc:HGNC:21494]","synonyms":"dJ403A15.3,C6orf174,dJ403A15.3,C6orf174","biotype":"protein_coding","ncbi_id":"387104","summary":null,"start":127472794,"end":127519191,"strand":-1,"description":"SOGA family member 3 [Source:HGNC Symbol;Acc:HGNC:21494]"}, {"versioned_ensembl_gene_id":"ENSG00000227412.1","gene_symbol":"STK33P1","gene_name":"serine/threonine kinase 33 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26871]","synonyms":"STK33ps,STK33P","biotype":"processed_pseudogene","ncbi_id":"553118","summary":null,"start":85492579,"end":85494094,"strand":1,"description":"serine/threonine kinase 33 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26871]"}, {"versioned_ensembl_gene_id":"ENSG00000104825.16","gene_symbol":"NFKBIB","gene_name":"NFKB inhibitor beta [Source:HGNC Symbol;Acc:HGNC:7798]","synonyms":"TRIP9,IKBB","biotype":"protein_coding","ncbi_id":"4793","summary":"The protein encoded by this gene belongs to the NF-kappa-B inhibitor family, which inhibit NF-kappa-B by complexing with, and trapping it in the cytoplasm. Phosphorylation of serine residues on these proteins by kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation of the NF-kappa-B, which translocates to the nucleus to function as a transcription factor. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jul 2011]","start":38899700,"end":38908893,"strand":1,"description":"NFKB inhibitor beta [Source:HGNC Symbol;Acc:HGNC:7798]"}, {"versioned_ensembl_gene_id":"ENSG00000278866.1","gene_symbol":"AC006065.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126675895,"end":126676243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257621.7","gene_symbol":"PSMA3-AS1","gene_name":"PSMA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26445]","synonyms":"FLJ31306","biotype":"antisense_RNA","ncbi_id":"379025","summary":null,"start":58265365,"end":58298134,"strand":-1,"description":"PSMA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26445]"}, {"versioned_ensembl_gene_id":"ENSG00000113712.17","gene_symbol":"CSNK1A1","gene_name":"casein kinase 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2451]","synonyms":"CKIalpha,CKIa,CK1alpha,CK1a,CK1","biotype":"protein_coding","ncbi_id":"1452","summary":null,"start":149492197,"end":149551552,"strand":-1,"description":"casein kinase 1 alpha 1 [Source:HGNC Symbol;Acc:HGNC:2451]"}, {"versioned_ensembl_gene_id":"ENSG00000242536.1","gene_symbol":"AC079943.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158016216,"end":158088997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249727.1","gene_symbol":"AC097494.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54836161,"end":54845402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226234.2","gene_symbol":"KRT18P24","gene_name":"keratin 18 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:33393]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340460","summary":null,"start":79036413,"end":79037568,"strand":-1,"description":"keratin 18 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:33393]"}, {"versioned_ensembl_gene_id":"ENSG00000135973.2","gene_symbol":"GPR45","gene_name":"G protein-coupled receptor 45 [Source:HGNC Symbol;Acc:HGNC:4503]","synonyms":"PSP24A,PSP24","biotype":"protein_coding","ncbi_id":"11250","summary":"This intronless gene encodes a member of the G protein-coupled receptor (GPCR) family. Members of this protein family contain seven putative transmembrane domains and may mediate signaling processes to the interior of the cell via activation of heterotrimeric G proteins. This protein may function in the central nervous system. [provided by RefSeq, Jul 2008]","start":105241743,"end":105243049,"strand":1,"description":"G protein-coupled receptor 45 [Source:HGNC Symbol;Acc:HGNC:4503]"}, {"versioned_ensembl_gene_id":"ENSG00000254124.1","gene_symbol":"EEF1A1P37","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:37915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421825","summary":null,"start":111225585,"end":111227049,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:37915]"}, {"versioned_ensembl_gene_id":"ENSG00000235342.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30686667,"end":30687396,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000206289.11","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"H-2RIIBP,RCoR-1,NR2B2","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33122398,"end":33129499,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000268240.1","gene_symbol":"AC123912.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21587432,"end":21594628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153012.11","gene_symbol":"LGI2","gene_name":"leucine rich repeat LGI family member 2 [Source:HGNC Symbol;Acc:HGNC:18710]","synonyms":"KIAA1916,FLJ10675","biotype":"protein_coding","ncbi_id":"55203","summary":null,"start":24998847,"end":25030879,"strand":-1,"description":"leucine rich repeat LGI family member 2 [Source:HGNC Symbol;Acc:HGNC:18710]"}, {"versioned_ensembl_gene_id":"ENSG00000224582.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507362","summary":null,"start":29529420,"end":29533665,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000260858.1","gene_symbol":"AC010551.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84255270,"end":84261049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120756.12","gene_symbol":"PLS1","gene_name":"plastin 1 [Source:HGNC Symbol;Acc:HGNC:9090]","synonyms":"Plastin-1,I-plastin","biotype":"protein_coding","ncbi_id":"5357","summary":"Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. The protein encoded by this gene is a third distinct plastin isoform, which is specifically expressed at high levels in the small intestine. Alternatively spliced transcript variants varying in the 5' UTR, but encoding the same protein, have been found for this gene. A pseudogene of this gene is found on chromosome 11.[provided by RefSeq, Feb 2010]","start":142596387,"end":142713664,"strand":1,"description":"plastin 1 [Source:HGNC Symbol;Acc:HGNC:9090]"}, {"versioned_ensembl_gene_id":"ENSG00000236374.1","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"KIAA0055-hom,D84394.7,USP8P","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31267736,"end":31270908,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000112139.14","gene_symbol":"MDGA1","gene_name":"MAM domain containing glycosylphosphatidylinositol anchor 1 [Source:HGNC Symbol;Acc:HGNC:19267]","synonyms":"MAMDC3,GPIM","biotype":"protein_coding","ncbi_id":"266727","summary":"This gene encodes a glycosylphosphatidylinositol (GPI)-anchored cell surface glycoprotein that is expressed predominantly in the developing nervous system. In addition to possessing several cell adhesion molecule-like domains, the mature protein has six Ig-like domains, a single fibronectin type III domain, a MAM domain and a C-terminal GPI-anchoring site. Studies in other mammals suggest this protein plays a role in cell adhesion, migration, and axon guidance and, in the developing brain, neuronal migration. In humans, this gene is associated with bipolar disorder and schizophrenia. [provided by RefSeq, Oct 2016]","start":37630679,"end":37699306,"strand":-1,"description":"MAM domain containing glycosylphosphatidylinositol anchor 1 [Source:HGNC Symbol;Acc:HGNC:19267]"}, {"versioned_ensembl_gene_id":"ENSG00000173681.16","gene_symbol":"BCLAF3","gene_name":"BCLAF1 and THRAP3 family member 3 [Source:HGNC Symbol;Acc:HGNC:27413]","synonyms":"CXorf23","biotype":"protein_coding","ncbi_id":"256643","summary":null,"start":19912860,"end":19970298,"strand":-1,"description":"BCLAF1 and THRAP3 family member 3 [Source:HGNC Symbol;Acc:HGNC:27413]"}, {"versioned_ensembl_gene_id":"ENSG00000239756.5","gene_symbol":"PHF1","gene_name":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]","synonyms":"MTF2L2,TDRD19C,PCL1","biotype":"processed_transcript","ncbi_id":"5252","summary":"This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":33339192,"end":33340037,"strand":1,"description":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]"}, {"versioned_ensembl_gene_id":"ENSG00000229949.1","gene_symbol":"AC005094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21400920,"end":21401613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279835.1","gene_symbol":"AL121785.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51098138,"end":51098845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248735.2","gene_symbol":"R3HDM2P1","gene_name":"R3H domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419742","summary":null,"start":133124104,"end":133126063,"strand":1,"description":"R3H domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44056]"}, {"versioned_ensembl_gene_id":"ENSG00000257543.1","gene_symbol":"AC063948.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101408372,"end":101409060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139641.12","gene_symbol":"ESYT1","gene_name":"extended synaptotagmin 1 [Source:HGNC Symbol;Acc:HGNC:29534]","synonyms":"MBC2,KIAA0747,FAM62A","biotype":"protein_coding","ncbi_id":"23344","summary":null,"start":56118250,"end":56144671,"strand":1,"description":"extended synaptotagmin 1 [Source:HGNC Symbol;Acc:HGNC:29534]"}, {"versioned_ensembl_gene_id":"ENSG00000249513.2","gene_symbol":"AC110751.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132985510,"end":132988677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280270.1","gene_symbol":"AC068299.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":187383101,"end":187384849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254795.1","gene_symbol":"OR5AP1P","gene_name":"olfactory receptor family 5 subfamily AP member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15257]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81223","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56633164,"end":56634103,"strand":-1,"description":"olfactory receptor family 5 subfamily AP member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15257]"}, {"versioned_ensembl_gene_id":"ENSG00000226885.1","gene_symbol":"E2F6P3","gene_name":"E2F transcription factor 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51451]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420178","summary":null,"start":21268161,"end":21268903,"strand":1,"description":"E2F transcription factor 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51451]"}, {"versioned_ensembl_gene_id":"ENSG00000226043.1","gene_symbol":"AP000561.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22209939,"end":22420819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231136.1","gene_symbol":"AP000705.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22153950,"end":22154299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283154.2","gene_symbol":"IQCJ-SCHIP1","gene_name":"IQCJ-SCHIP1 readthrough [Source:HGNC Symbol;Acc:HGNC:38842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505385","summary":"This locus represents naturally occurring read-through transcription from the neighboring IQ motif containing J (IQCJ) and schwannomin interacting protein 1 (SCHIP1) genes. Alternative splicing results in multiple transcript variants that are composed of in-frame exons from each individual gene. The resulting fusion products are thought to be components of the multimolecular complexes of axon initial segments and nodes of Ranvier, and they may play a role in calcium-mediated responses. [provided by RefSeq, Oct 2010]","start":158962235,"end":159897366,"strand":1,"description":"IQCJ-SCHIP1 readthrough [Source:HGNC Symbol;Acc:HGNC:38842]"}, {"versioned_ensembl_gene_id":"ENSG00000169446.5","gene_symbol":"MMGT1","gene_name":"membrane magnesium transporter 1 [Source:HGNC Symbol;Acc:HGNC:28100]","synonyms":"EMC5,TMEM32","biotype":"protein_coding","ncbi_id":"93380","summary":null,"start":135962070,"end":135974063,"strand":-1,"description":"membrane magnesium transporter 1 [Source:HGNC Symbol;Acc:HGNC:28100]"}, {"versioned_ensembl_gene_id":"ENSG00000265984.1","gene_symbol":"AC022809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21240675,"end":21241371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255221.3","gene_symbol":"CARD17","gene_name":"caspase recruitment domain family member 17 [Source:HGNC Symbol;Acc:HGNC:33827]","synonyms":"INCA","biotype":"protein_coding","ncbi_id":"440068","summary":null,"start":105092469,"end":105101431,"strand":-1,"description":"caspase recruitment domain family member 17 [Source:HGNC Symbol;Acc:HGNC:33827]"}, {"versioned_ensembl_gene_id":"ENSG00000266237.1","gene_symbol":"AC121320.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26266009,"end":26267409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145730.20","gene_symbol":"PAM","gene_name":"peptidylglycine alpha-amidating monooxygenase [Source:HGNC Symbol;Acc:HGNC:8596]","synonyms":"PHM,PAL","biotype":"protein_coding","ncbi_id":"5066","summary":"This gene encodes a multifunctional protein. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme includes two domains with distinct catalytic activities, a peptidylglycine alpha-hydroxylating monooxygenase (PHM) domain and a peptidyl-alpha-hydroxyglycine alpha-amidating lyase (PAL) domain. These catalytic domains work sequentially to catalyze the conversion of neuroendocrine peptides to active alpha-amidated products. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":102753981,"end":103031105,"strand":1,"description":"peptidylglycine alpha-amidating monooxygenase [Source:HGNC Symbol;Acc:HGNC:8596]"}, {"versioned_ensembl_gene_id":"ENSG00000198937.8","gene_symbol":"CCDC167","gene_name":"coiled-coil domain containing 167 [Source:HGNC Symbol;Acc:HGNC:21239]","synonyms":"dJ153P14.2,C6orf129","biotype":"protein_coding","ncbi_id":"154467","summary":null,"start":37482920,"end":37499922,"strand":-1,"description":"coiled-coil domain containing 167 [Source:HGNC Symbol;Acc:HGNC:21239]"}, {"versioned_ensembl_gene_id":"ENSG00000124217.4","gene_symbol":"MOCS3","gene_name":"molybdenum cofactor synthesis 3 [Source:HGNC Symbol;Acc:HGNC:15765]","synonyms":"UBA4,dJ914P20.3","biotype":"protein_coding","ncbi_id":"27304","summary":"Molybdenum cofactor (MoCo) is necessary for the function of all molybdoenzymes. The protein encoded by this gene adenylates and activates molybdopterin synthase, an enzyme required for biosynthesis of MoCo. This gene contains no introns. A pseudogene of this gene is present on chromosome 14. [provided by RefSeq, Nov 2012]","start":50958826,"end":50963931,"strand":1,"description":"molybdenum cofactor synthesis 3 [Source:HGNC Symbol;Acc:HGNC:15765]"}, {"versioned_ensembl_gene_id":"ENSG00000235427.1","gene_symbol":"AC006159.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116542718,"end":116551969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188171.15","gene_symbol":"ZNF626","gene_name":"zinc finger protein 626 [Source:HGNC Symbol;Acc:HGNC:30461]","synonyms":null,"biotype":"protein_coding","ncbi_id":"199777","summary":null,"start":20620061,"end":20661596,"strand":-1,"description":"zinc finger protein 626 [Source:HGNC Symbol;Acc:HGNC:30461]"}, {"versioned_ensembl_gene_id":"ENSG00000196296.13","gene_symbol":"ATP2A1","gene_name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:811]","synonyms":"SERCA1,ATP2A","biotype":"protein_coding","ncbi_id":"487","summary":"This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Oct 2013]","start":28878405,"end":28904509,"strand":1,"description":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:811]"}, {"versioned_ensembl_gene_id":"ENSG00000073756.11","gene_symbol":"PTGS2","gene_name":"prostaglandin-endoperoxide synthase 2 [Source:HGNC Symbol;Acc:HGNC:9605]","synonyms":"COX2","biotype":"protein_coding","ncbi_id":"5743","summary":"Prostaglandin-endoperoxide synthase (PTGS), also known as cyclooxygenase, is the key enzyme in prostaglandin biosynthesis, and acts both as a dioxygenase and as a peroxidase. There are two isozymes of PTGS: a constitutive PTGS1 and an inducible PTGS2, which differ in their regulation of expression and tissue distribution. This gene encodes the inducible isozyme. It is regulated by specific stimulatory events, suggesting that it is responsible for the prostanoid biosynthesis involved in inflammation and mitogenesis. [provided by RefSeq, Feb 2009]","start":186671791,"end":186680427,"strand":-1,"description":"prostaglandin-endoperoxide synthase 2 [Source:HGNC Symbol;Acc:HGNC:9605]"}, {"versioned_ensembl_gene_id":"ENSG00000270343.1","gene_symbol":"UNGP3","gene_name":"uracil-DNA glycosylase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20036]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319122","summary":null,"start":81259565,"end":81260239,"strand":-1,"description":"uracil-DNA glycosylase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:20036]"}, {"versioned_ensembl_gene_id":"ENSG00000069702.10","gene_symbol":"TGFBR3","gene_name":"transforming growth factor beta receptor 3 [Source:HGNC Symbol;Acc:HGNC:11774]","synonyms":"BGCAN,betaglycan","biotype":"protein_coding","ncbi_id":"7049","summary":"This locus encodes the transforming growth factor (TGF)-beta type III receptor. The encoded receptor is a membrane proteoglycan that often functions as a co-receptor with other TGF-beta receptor superfamily members. Ectodomain shedding produces soluble TGFBR3, which may inhibit TGFB signaling. Decreased expression of this receptor has been observed in various cancers. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.[provided by RefSeq, Sep 2010]","start":91680343,"end":91906335,"strand":-1,"description":"transforming growth factor beta receptor 3 [Source:HGNC Symbol;Acc:HGNC:11774]"}, {"versioned_ensembl_gene_id":"ENSG00000279199.1","gene_symbol":"AC068669.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40113215,"end":40115442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108465.14","gene_symbol":"CDK5RAP3","gene_name":"CDK5 regulatory subunit associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18673]","synonyms":"OK/SW-cl.114,MST016,LZAP,IC53,HSF-27,FLJ13660,C53","biotype":"protein_coding","ncbi_id":"80279","summary":"This gene encodes a protein that has been reported to function in signaling pathways governing transcriptional regulation and cell cycle progression. It may play a role in tumorigenesis and metastasis. A pseudogene of this gene is located on the long arm of chromosome 20. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, May 2013]","start":47967810,"end":47981774,"strand":1,"description":"CDK5 regulatory subunit associated protein 3 [Source:HGNC Symbol;Acc:HGNC:18673]"}, {"versioned_ensembl_gene_id":"ENSG00000203870.5","gene_symbol":"SMIM9","gene_name":"small integral membrane protein 9 [Source:HGNC Symbol;Acc:HGNC:41915]","synonyms":"CXorf68","biotype":"protein_coding","ncbi_id":"100132963","summary":null,"start":154823348,"end":154834662,"strand":-1,"description":"small integral membrane protein 9 [Source:HGNC Symbol;Acc:HGNC:41915]"}, {"versioned_ensembl_gene_id":"ENSG00000229384.2","gene_symbol":"HMGB1P16","gene_name":"high mobility group box 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39098]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646577","summary":null,"start":36211096,"end":36211635,"strand":1,"description":"high mobility group box 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39098]"}, {"versioned_ensembl_gene_id":"ENSG00000263798.2","gene_symbol":"AC018521.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":47945424,"end":47981736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270829.1","gene_symbol":"AC015849.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35808489,"end":35808897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232374.5","gene_symbol":"GPR79","gene_name":"G protein-coupled receptor 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:4529]","synonyms":"GPR79P","biotype":"processed_pseudogene","ncbi_id":"27200","summary":null,"start":158841093,"end":158841960,"strand":-1,"description":"G protein-coupled receptor 79, pseudogene [Source:HGNC Symbol;Acc:HGNC:4529]"}, {"versioned_ensembl_gene_id":"ENSG00000249721.1","gene_symbol":"AC112206.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67692812,"end":67693200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255466.1","gene_symbol":"OR5AL2P","gene_name":"olfactory receptor family 5 subfamily AL member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14850]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79476","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56393729,"end":56394648,"strand":1,"description":"olfactory receptor family 5 subfamily AL member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14850]"}, {"versioned_ensembl_gene_id":"ENSG00000249347.1","gene_symbol":"AC073648.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8990455,"end":8990806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225554.1","gene_symbol":"AL359764.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241424292,"end":241433492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253111.1","gene_symbol":"AC091114.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125466939,"end":125541373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248955.1","gene_symbol":"AC113367.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131008583,"end":131008742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165204.3","gene_symbol":"OR1K1","gene_name":"olfactory receptor family 1 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:8212]","synonyms":"MNAB,hg99","biotype":"protein_coding","ncbi_id":"392392","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122800123,"end":122801073,"strand":1,"description":"olfactory receptor family 1 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:8212]"}, {"versioned_ensembl_gene_id":"ENSG00000249415.1","gene_symbol":"BX908738.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29268443,"end":29269402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105699.16","gene_symbol":"LSR","gene_name":"lipolysis stimulated lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:29572]","synonyms":"ILDR3,LISCH7","biotype":"protein_coding","ncbi_id":"51599","summary":null,"start":35248330,"end":35267964,"strand":1,"description":"lipolysis stimulated lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:29572]"}, {"versioned_ensembl_gene_id":"ENSG00000228528.1","gene_symbol":"AC068057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104703758,"end":104705509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234119.1","gene_symbol":"AC079248.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145826285,"end":145827830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279297.1","gene_symbol":"AP000720.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89297717,"end":89298199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226783.1","gene_symbol":"TLK1P1","gene_name":"tousled like kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28608]","synonyms":"TLK1ps,TLK1P","biotype":"processed_pseudogene","ncbi_id":"100129793","summary":null,"start":122685933,"end":122688372,"strand":1,"description":"tousled like kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28608]"}, {"versioned_ensembl_gene_id":"ENSG00000224666.3","gene_symbol":"Z84484.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36386831,"end":36393462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180483.6","gene_symbol":"DEFB119","gene_name":"defensin beta 119 [Source:HGNC Symbol;Acc:HGNC:18099]","synonyms":"DEFB120,DEFB-20,DEFB-19","biotype":"protein_coding","ncbi_id":"245932","summary":"This gene encodes a member of the beta subfamily of defensins. Beta-defensins are antimicrobial peptides that protect tissues and organs from infection by a variety of microorganisms. This gene is found in a cluster with other beta-defensin genes on the long arm of chromosome 20. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":31377164,"end":31390603,"strand":-1,"description":"defensin beta 119 [Source:HGNC Symbol;Acc:HGNC:18099]"}, {"versioned_ensembl_gene_id":"ENSG00000175868.13","gene_symbol":"CALCB","gene_name":"calcitonin related polypeptide beta [Source:HGNC Symbol;Acc:HGNC:1438]","synonyms":"FLJ30166,CGRP-II,CALC2","biotype":"protein_coding","ncbi_id":"797","summary":null,"start":14904997,"end":15082342,"strand":1,"description":"calcitonin related polypeptide beta [Source:HGNC Symbol;Acc:HGNC:1438]"}, {"versioned_ensembl_gene_id":"ENSG00000179165.10","gene_symbol":"PXT1","gene_name":"peroxisomal, testis specific 1 [Source:HGNC Symbol;Acc:HGNC:18312]","synonyms":"STEPP","biotype":"protein_coding","ncbi_id":"222659","summary":null,"start":36390551,"end":36442889,"strand":-1,"description":"peroxisomal, testis specific 1 [Source:HGNC Symbol;Acc:HGNC:18312]"}, {"versioned_ensembl_gene_id":"ENSG00000153563.15","gene_symbol":"CD8A","gene_name":"CD8a molecule [Source:HGNC Symbol;Acc:HGNC:1706]","synonyms":"CD8","biotype":"protein_coding","ncbi_id":"925","summary":"The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen acts as a coreceptor with the T-cell receptor on the T lymphocyte to recognize antigens displayed by an antigen presenting cell in the context of class I MHC molecules. The coreceptor functions as either a homodimer composed of two alpha chains or as a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 alpha chain. Multiple transcript variants encoding different isoforms have been found for this gene. The major protein isoforms of this gene differ by the presence or absence of a transmembrane domain and thus differ in being a membrane-anchored or secreted protein. [provided by RefSeq, May 2020]","start":86784610,"end":86808396,"strand":-1,"description":"CD8a molecule [Source:HGNC Symbol;Acc:HGNC:1706]"}, {"versioned_ensembl_gene_id":"ENSG00000021826.14","gene_symbol":"CPS1","gene_name":"carbamoyl-phosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:2323]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1373","summary":"The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.[provided by RefSeq, May 2010]","start":210477682,"end":210679107,"strand":1,"description":"carbamoyl-phosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:2323]"}, {"versioned_ensembl_gene_id":"ENSG00000249412.1","gene_symbol":"AC010285.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179963615,"end":179964419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239590.1","gene_symbol":"OR1J4","gene_name":"olfactory receptor family 1 subfamily J member 4 [Source:HGNC Symbol;Acc:HGNC:8211]","synonyms":"HTPCRX01,HSHTPCRX01","biotype":"protein_coding","ncbi_id":"26219","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122519141,"end":122520082,"strand":1,"description":"olfactory receptor family 1 subfamily J member 4 [Source:HGNC Symbol;Acc:HGNC:8211]"}, {"versioned_ensembl_gene_id":"ENSG00000203791.14","gene_symbol":"EEF1AKMT2","gene_name":"EEF1A lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:33787]","synonyms":"METTL10,Efm4,C10orf138","biotype":"protein_coding","ncbi_id":"399818","summary":null,"start":124748149,"end":124791870,"strand":-1,"description":"EEF1A lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:33787]"}, {"versioned_ensembl_gene_id":"ENSG00000250437.1","gene_symbol":"LINC02161","gene_name":"long intergenic non-protein coding RNA 2161 [Source:HGNC Symbol;Acc:HGNC:53022]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379076","summary":null,"start":89581209,"end":89677701,"strand":1,"description":"long intergenic non-protein coding RNA 2161 [Source:HGNC Symbol;Acc:HGNC:53022]"}, {"versioned_ensembl_gene_id":"ENSG00000162390.17","gene_symbol":"ACOT11","gene_name":"acyl-CoA thioesterase 11 [Source:HGNC Symbol;Acc:HGNC:18156]","synonyms":"THEM1,THEA,STARD14,KIAA0707,BFIT1,BFIT","biotype":"protein_coding","ncbi_id":"26027","summary":"This gene encodes a member of the acyl-CoA thioesterase family which catalyse the conversion of activated fatty acids to the corresponding non-esterified fatty acid and coenzyme A. Expression of a mouse homolog in brown adipose tissue is induced by low temperatures and repressed by warm temperatures. Higher levels of expression of the mouse homolog has been found in obesity-resistant mice compared with obesity-prone mice, suggesting a role of acyl-CoA thioesterase 11 in obesity. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010]","start":54542257,"end":54639192,"strand":1,"description":"acyl-CoA thioesterase 11 [Source:HGNC Symbol;Acc:HGNC:18156]"}, {"versioned_ensembl_gene_id":"ENSG00000278831.1","gene_symbol":"AL513190.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124623353,"end":124624079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229455.2","gene_symbol":"RPS10P18","gene_name":"ribosomal protein S10 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271349","summary":null,"start":124489823,"end":124490578,"strand":-1,"description":"ribosomal protein S10 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36239]"}, {"versioned_ensembl_gene_id":"ENSG00000187905.10","gene_symbol":"LRRC74B","gene_name":"leucine rich repeat containing 74B [Source:HGNC Symbol;Acc:HGNC:34301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400891","summary":null,"start":21045960,"end":21064168,"strand":1,"description":"leucine rich repeat containing 74B [Source:HGNC Symbol;Acc:HGNC:34301]"}, {"versioned_ensembl_gene_id":"ENSG00000258626.2","gene_symbol":"AL049779.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67652300,"end":67652614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124299.13","gene_symbol":"PEPD","gene_name":"peptidase D [Source:HGNC Symbol;Acc:HGNC:8840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5184","summary":"This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline, and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency, which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":33386950,"end":33521794,"strand":-1,"description":"peptidase D [Source:HGNC Symbol;Acc:HGNC:8840]"}, {"versioned_ensembl_gene_id":"ENSG00000118094.11","gene_symbol":"TREH","gene_name":"trehalase [Source:HGNC Symbol;Acc:HGNC:12266]","synonyms":"TREA,TRE,MGC129621","biotype":"protein_coding","ncbi_id":"11181","summary":"This gene encodes an enzyme that hydrolyses trehalose, a disaccharide formed from two glucose molecules found mainly in fungi, plants, and insects. A partial duplication of this gene is located adjacent to this locus on chromosome 11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":118657316,"end":118679690,"strand":-1,"description":"trehalase [Source:HGNC Symbol;Acc:HGNC:12266]"}, {"versioned_ensembl_gene_id":"ENSG00000235721.1","gene_symbol":"AC013268.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110007675,"end":110010783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233019.1","gene_symbol":"CR547123.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071788,"end":29072563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086300.15","gene_symbol":"SNX10","gene_name":"sorting nexin 10 [Source:HGNC Symbol;Acc:HGNC:14974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29887","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene may play a role in regulating endosome homeostasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":26291895,"end":26374329,"strand":1,"description":"sorting nexin 10 [Source:HGNC Symbol;Acc:HGNC:14974]"}, {"versioned_ensembl_gene_id":"ENSG00000228197.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"bA150A6.3,DDX6P,DDX6-Lp","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29329677,"end":29331112,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000042781.12","gene_symbol":"USH2A","gene_name":"usherin [Source:HGNC Symbol;Acc:HGNC:12601]","synonyms":"USH2,RP39","biotype":"protein_coding","ncbi_id":"7399","summary":"This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":215622894,"end":216423396,"strand":-1,"description":"usherin [Source:HGNC Symbol;Acc:HGNC:12601]"}, {"versioned_ensembl_gene_id":"ENSG00000237777.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29306740,"end":29307705,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000066583.11","gene_symbol":"ISOC1","gene_name":"isochorismatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24254]","synonyms":"CGI-111","biotype":"protein_coding","ncbi_id":"51015","summary":null,"start":129094751,"end":129114028,"strand":1,"description":"isochorismatase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24254]"}, {"versioned_ensembl_gene_id":"ENSG00000275263.1","gene_symbol":"AC135048.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30956872,"end":30957199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223866.1","gene_symbol":"AC002486.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20641558,"end":20641948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238256.1","gene_symbol":"MTND5P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873269","summary":null,"start":113576757,"end":113576899,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42300]"}, {"versioned_ensembl_gene_id":"ENSG00000232499.2","gene_symbol":"AL391058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113449700,"end":113450728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203279.3","gene_symbol":"AL590705.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97200475,"end":97238700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221849.2","gene_symbol":"AC018880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103527620,"end":103529261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262986.1","gene_symbol":"SMIM10L1","gene_name":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129361","summary":null,"start":11203312,"end":11203513,"strand":1,"description":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]"}, {"versioned_ensembl_gene_id":"ENSG00000230233.1","gene_symbol":"AF240627.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18614431,"end":18650360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232529.1","gene_symbol":"AL031773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155380511,"end":155381183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280307.1","gene_symbol":"AP000676.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87879473,"end":87880095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226919.1","gene_symbol":"AL365184.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240765557,"end":240768680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196468.7","gene_symbol":"FGF16","gene_name":"fibroblast growth factor 16 [Source:HGNC Symbol;Acc:HGNC:3672]","synonyms":"MF4","biotype":"protein_coding","ncbi_id":"8823","summary":"This gene encodes a member of a family of proteins that are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene is expressed in cardiac cells and is required for proper heart development. Mutation in this gene was also observed in individuals with metacarpal 4-5 fusion. [provided by RefSeq, Mar 2014]","start":77447405,"end":77457278,"strand":1,"description":"fibroblast growth factor 16 [Source:HGNC Symbol;Acc:HGNC:3672]"}, {"versioned_ensembl_gene_id":"ENSG00000280327.1","gene_symbol":"Z97633.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1576716,"end":1578371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224320.9","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29879141,"end":29999464,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000255316.1","gene_symbol":"MTND6P25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:51984]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075262","summary":null,"start":81555910,"end":81556425,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:51984]"}, {"versioned_ensembl_gene_id":"ENSG00000228217.1","gene_symbol":"PNRC2P1","gene_name":"proline rich nuclear receptor coactivator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131261","summary":null,"start":117778087,"end":117778506,"strand":-1,"description":"proline rich nuclear receptor coactivator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51933]"}, {"versioned_ensembl_gene_id":"ENSG00000255178.1","gene_symbol":"AP002759.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80751200,"end":80762826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254437.1","gene_symbol":"AP003398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80957317,"end":80957634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227187.1","gene_symbol":"AC007435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175033778,"end":175034192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186297.11","gene_symbol":"GABRA5","gene_name":"gamma-aminobutyric acid type A receptor alpha5 subunit [Source:HGNC Symbol;Acc:HGNC:4079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2558","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. Transcript variants utilizing three different alternative non-coding first exons have been described. [provided by RefSeq, Jul 2008]","start":26866363,"end":26949207,"strand":1,"description":"gamma-aminobutyric acid type A receptor alpha5 subunit [Source:HGNC Symbol;Acc:HGNC:4079]"}, {"versioned_ensembl_gene_id":"ENSG00000224118.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29849539,"end":29849688,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000231998.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29899284,"end":29900148,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000230648.1","gene_symbol":"AL138831.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4018843,"end":4021215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139131.12","gene_symbol":"YARS2","gene_name":"tyrosyl-tRNA synthetase 2 [Source:HGNC Symbol;Acc:HGNC:24249]","synonyms":"mt-TyrRS,FLJ13995,CGI-04","biotype":"protein_coding","ncbi_id":"51067","summary":"This gene encodes a mitochondrial protein that catalyzes the attachment of tyrosine to tRNA(Tyr). Mutations in this gene are associated with myopathy with lactic acidosis and sideroblastic anemia type 2 (MLASA2). [provided by RefSeq, Jan 2011]","start":32727490,"end":32755902,"strand":-1,"description":"tyrosyl-tRNA synthetase 2 [Source:HGNC Symbol;Acc:HGNC:24249]"}, {"versioned_ensembl_gene_id":"ENSG00000216657.1","gene_symbol":"GLRX3P2","gene_name":"glutaredoxin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49788]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728344","summary":null,"start":3978062,"end":3979099,"strand":1,"description":"glutaredoxin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49788]"}, {"versioned_ensembl_gene_id":"ENSG00000164830.18","gene_symbol":"OXR1","gene_name":"oxidation resistance 1 [Source:HGNC Symbol;Acc:HGNC:15822]","synonyms":"TLDC3","biotype":"protein_coding","ncbi_id":"55074","summary":null,"start":106359476,"end":106752694,"strand":1,"description":"oxidation resistance 1 [Source:HGNC Symbol;Acc:HGNC:15822]"}, {"versioned_ensembl_gene_id":"ENSG00000123892.11","gene_symbol":"RAB38","gene_name":"RAB38, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9776]","synonyms":"NY-MEL-1","biotype":"protein_coding","ncbi_id":"23682","summary":null,"start":88113242,"end":88175467,"strand":-1,"description":"RAB38, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9776]"}, {"versioned_ensembl_gene_id":"ENSG00000229167.1","gene_symbol":"AC114488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31571585,"end":31575573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230513.1","gene_symbol":"THAP7-AS1","gene_name":"THAP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41013]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"439931","summary":null,"start":21001886,"end":21010342,"strand":1,"description":"THAP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41013]"}, {"versioned_ensembl_gene_id":"ENSG00000238158.6","gene_symbol":"AL391422.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3831933,"end":3855737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284130.1","gene_symbol":"AC002472.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21011384,"end":21014217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228744.1","gene_symbol":"AF228730.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7122857,"end":7123704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108588.13","gene_symbol":"CCDC47","gene_name":"coiled-coil domain containing 47 [Source:HGNC Symbol;Acc:HGNC:24856]","synonyms":"GK001","biotype":"protein_coding","ncbi_id":"57003","summary":null,"start":63745250,"end":63776351,"strand":-1,"description":"coiled-coil domain containing 47 [Source:HGNC Symbol;Acc:HGNC:24856]"}, {"versioned_ensembl_gene_id":"ENSG00000284656.1","gene_symbol":"AL645937.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29162475,"end":29166201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259266.1","gene_symbol":"AC022523.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98118171,"end":98118320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257298.1","gene_symbol":"AC008147.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50185580,"end":50191363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227922.1","gene_symbol":"SPTLC1P5","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39672]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874512","summary":null,"start":77659413,"end":77659664,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39672]"}, {"versioned_ensembl_gene_id":"ENSG00000101972.18","gene_symbol":"STAG2","gene_name":"stromal antigen 2 [Source:HGNC Symbol;Acc:HGNC:11355]","synonyms":"SA-2,SCC3B,SA2","biotype":"protein_coding","ncbi_id":"10735","summary":"The protein encoded by this gene is a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division. Targeted inactivation of this gene results in chromatid cohesion defects and aneuploidy, suggesting that genetic disruption of cohesin is a cause of aneuploidy in human cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":123960212,"end":124422664,"strand":1,"description":"stromal antigen 2 [Source:HGNC Symbol;Acc:HGNC:11355]"}, {"versioned_ensembl_gene_id":"ENSG00000282995.1","gene_symbol":"FRG1EP","gene_name":"FSHD region gene 1 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:51764]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723390","summary":null,"start":29480147,"end":29497179,"strand":-1,"description":"FSHD region gene 1 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:51764]"}, {"versioned_ensembl_gene_id":"ENSG00000206145.8","gene_symbol":"P2RX6P","gene_name":"purinergic receptor P2X 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:34076]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440799","summary":null,"start":21035243,"end":21045017,"strand":-1,"description":"purinergic receptor P2X 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:34076]"}, {"versioned_ensembl_gene_id":"ENSG00000214700.5","gene_symbol":"C12orf71","gene_name":"chromosome 12 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34452]","synonyms":"LOC728858","biotype":"protein_coding","ncbi_id":"728858","summary":null,"start":27081058,"end":27082514,"strand":-1,"description":"chromosome 12 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34452]"}, {"versioned_ensembl_gene_id":"ENSG00000230447.2","gene_symbol":"CTF2P","gene_name":"cardiotrophin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33173]","synonyms":"NP","biotype":"unitary_pseudogene","ncbi_id":"100289419","summary":"The cytokine neuropoietin belongs to the IL-6 superfamily. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Mar 2013]","start":30904348,"end":30910208,"strand":-1,"description":"cardiotrophin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33173]"}, {"versioned_ensembl_gene_id":"ENSG00000224359.2","gene_symbol":"AL358176.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240530452,"end":240530862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116005.11","gene_symbol":"PCYOX1","gene_name":"prenylcysteine oxidase 1 [Source:HGNC Symbol;Acc:HGNC:20588]","synonyms":"PCL1,KIAA0908","biotype":"protein_coding","ncbi_id":"51449","summary":"Prenylcysteine is released during the degradation of prenylated proteins. PCYOX1 catalyzes the degradation of prenylcysteine to yield free cysteines and a hydrophobic isoprenoid product (Tschantz et al., 1999 [PubMed 10585463]).[supplied by OMIM, Mar 2008]","start":70257386,"end":70281191,"strand":1,"description":"prenylcysteine oxidase 1 [Source:HGNC Symbol;Acc:HGNC:20588]"}, {"versioned_ensembl_gene_id":"ENSG00000231160.9","gene_symbol":"KLF3-AS1","gene_name":"KLF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25796]","synonyms":"FLJ13197","biotype":"processed_transcript","ncbi_id":"79667","summary":null,"start":38612701,"end":38664883,"strand":-1,"description":"KLF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25796]"}, {"versioned_ensembl_gene_id":"ENSG00000148308.17","gene_symbol":"GTF3C5","gene_name":"general transcription factor IIIC subunit 5 [Source:HGNC Symbol;Acc:HGNC:4668]","synonyms":"TFIIICepsilon,TFIIIC63,TFiiiC2-63","biotype":"protein_coding","ncbi_id":"9328","summary":null,"start":133030675,"end":133058503,"strand":1,"description":"general transcription factor IIIC subunit 5 [Source:HGNC Symbol;Acc:HGNC:4668]"}, {"versioned_ensembl_gene_id":"ENSG00000226014.1","gene_symbol":"AL358176.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240549867,"end":240550378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123965.13","gene_symbol":"PMS2P5","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:9130]","synonyms":"PMS7,PMS2L5,MGC34222","biotype":"unprocessed_pseudogene","ncbi_id":"5383","summary":null,"start":74894116,"end":74897835,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:9130]"}, {"versioned_ensembl_gene_id":"ENSG00000187187.13","gene_symbol":"ZNF546","gene_name":"zinc finger protein 546 [Source:HGNC Symbol;Acc:HGNC:28671]","synonyms":"ZNF49,MGC43537","biotype":"protein_coding","ncbi_id":"339327","summary":null,"start":39984134,"end":40021041,"strand":1,"description":"zinc finger protein 546 [Source:HGNC Symbol;Acc:HGNC:28671]"}, {"versioned_ensembl_gene_id":"ENSG00000068654.15","gene_symbol":"POLR1A","gene_name":"RNA polymerase I subunit A [Source:HGNC Symbol;Acc:HGNC:17264]","synonyms":"RPO1-4,RPA1,FLJ21915,DKFZP586M0122","biotype":"protein_coding","ncbi_id":"25885","summary":"The protein encoded by this gene is the largest subunit of the RNA polymerase I complex. The encoded protein represents the catalytic subunit of the complex, which transcribes DNA into ribosomal RNA precursors. Defects in this gene are a cause of the Cincinnati type of acrofacial dysostosis. [provided by RefSeq, May 2016]","start":86020216,"end":86106155,"strand":-1,"description":"RNA polymerase I subunit A [Source:HGNC Symbol;Acc:HGNC:17264]"}, {"versioned_ensembl_gene_id":"ENSG00000180875.4","gene_symbol":"GREM2","gene_name":"gremlin 2, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:17655]","synonyms":"Prdc,FLJ21195,DAND3,CKTSF1B2","biotype":"protein_coding","ncbi_id":"64388","summary":"This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted glycosylated protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. [provided by RefSeq, Jul 2008]","start":240489573,"end":240612149,"strand":-1,"description":"gremlin 2, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:17655]"}, {"versioned_ensembl_gene_id":"ENSG00000075461.5","gene_symbol":"CACNG4","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:1408]","synonyms":"MGC24983,MGC11138","biotype":"protein_coding","ncbi_id":"27092","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type II TARP and a calcium channel gamma subunit. [provided by RefSeq, Dec 2010]","start":66964910,"end":67033398,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:1408]"}, {"versioned_ensembl_gene_id":"ENSG00000254135.2","gene_symbol":"AC091939.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158485190,"end":158588546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213373.7","gene_symbol":"LINC00671","gene_name":"long intergenic non-protein coding RNA 671 [Source:HGNC Symbol;Acc:HGNC:44339]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388387","summary":null,"start":42874670,"end":42898704,"strand":-1,"description":"long intergenic non-protein coding RNA 671 [Source:HGNC Symbol;Acc:HGNC:44339]"}, {"versioned_ensembl_gene_id":"ENSG00000235775.1","gene_symbol":"AC063976.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":132163603,"end":132163765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279117.1","gene_symbol":"AP001972.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75260129,"end":75262466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254963.1","gene_symbol":"AP001972.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75264289,"end":75265170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149305.6","gene_symbol":"HTR3B","gene_name":"5-hydroxytryptamine receptor 3B [Source:HGNC Symbol;Acc:HGNC:5298]","synonyms":"5-HT3B","biotype":"protein_coding","ncbi_id":"9177","summary":"The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit B of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor causes fast, depolarizing responses in neurons after activation. It is not functional as a homomeric complex, but a pentaheteromeric complex with subunit A (HTR3A) displays the full functional features of this receptor. [provided by RefSeq, Aug 2011]","start":113904677,"end":113946565,"strand":1,"description":"5-hydroxytryptamine receptor 3B [Source:HGNC Symbol;Acc:HGNC:5298]"}, {"versioned_ensembl_gene_id":"ENSG00000142233.11","gene_symbol":"NTN5","gene_name":"netrin 5 [Source:HGNC Symbol;Acc:HGNC:25208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126147","summary":null,"start":48661407,"end":48673081,"strand":-1,"description":"netrin 5 [Source:HGNC Symbol;Acc:HGNC:25208]"}, {"versioned_ensembl_gene_id":"ENSG00000259721.1","gene_symbol":"AC090877.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32717270,"end":32719007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248655.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"dJ207F6.1,NOL5BP,NOL5B,NOP56-L","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28784437,"end":28784808,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000178568.14","gene_symbol":"ERBB4","gene_name":"erb-b2 receptor tyrosine kinase 4 [Source:HGNC Symbol;Acc:HGNC:3432]","synonyms":"HER4,ALS19","biotype":"protein_coding","ncbi_id":"2066","summary":"This gene is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily. It encodes a single-pass type I membrane protein with multiple cysteine rich domains, a transmembrane domain, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins and other factors and induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment. Mutations in this gene have been associated with cancer. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":211375717,"end":212538841,"strand":-1,"description":"erb-b2 receptor tyrosine kinase 4 [Source:HGNC Symbol;Acc:HGNC:3432]"}, {"versioned_ensembl_gene_id":"ENSG00000241183.1","gene_symbol":"AC009022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70079129,"end":70079624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270965.1","gene_symbol":"NTAN1P1","gene_name":"N-terminal asparagine amidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45261]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420389","summary":null,"start":115819842,"end":115820487,"strand":-1,"description":"N-terminal asparagine amidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45261]"}, {"versioned_ensembl_gene_id":"ENSG00000237443.1","gene_symbol":"OR13D2P","gene_name":"olfactory receptor family 13 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15105]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392375","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104590044,"end":104590950,"strand":1,"description":"olfactory receptor family 13 subfamily D member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15105]"}, {"versioned_ensembl_gene_id":"ENSG00000170270.4","gene_symbol":"GON7","gene_name":"GON7, KEOPS complex subunit homolog [Source:HGNC Symbol;Acc:HGNC:20356]","synonyms":"C14orf142","biotype":"protein_coding","ncbi_id":"84520","summary":null,"start":93202894,"end":93207094,"strand":-1,"description":"GON7, KEOPS complex subunit homolog [Source:HGNC Symbol;Acc:HGNC:20356]"}, {"versioned_ensembl_gene_id":"ENSG00000131126.18","gene_symbol":"TEX101","gene_name":"testis expressed 101 [Source:HGNC Symbol;Acc:HGNC:30722]","synonyms":"SPATA44,SGRG,MGC4766,CT131","biotype":"protein_coding","ncbi_id":"83639","summary":null,"start":43401496,"end":43418597,"strand":1,"description":"testis expressed 101 [Source:HGNC Symbol;Acc:HGNC:30722]"}, {"versioned_ensembl_gene_id":"ENSG00000265784.1","gene_symbol":"AC006441.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38918801,"end":38921769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123836.14","gene_symbol":"PFKFB2","gene_name":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:8873]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5208","summary":"The protein encoded by this gene is involved in both the synthesis and degradation of fructose-2,6-bisphosphate, a regulatory molecule that controls glycolysis in eukaryotes. The encoded protein has a 6-phosphofructo-2-kinase activity that catalyzes the synthesis of fructose-2,6-bisphosphate, and a fructose-2,6-biphosphatase activity that catalyzes the degradation of fructose-2,6-bisphosphate. This protein regulates fructose-2,6-bisphosphate levels in the heart, while a related enzyme encoded by a different gene regulates fructose-2,6-bisphosphate levels in the liver and muscle. This enzyme functions as a homodimer. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":207034366,"end":207081024,"strand":1,"description":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:8873]"}, {"versioned_ensembl_gene_id":"ENSG00000159346.12","gene_symbol":"ADIPOR1","gene_name":"adiponectin receptor 1 [Source:HGNC Symbol;Acc:HGNC:24040]","synonyms":"PAQR1,ACDCR1","biotype":"protein_coding","ncbi_id":"51094","summary":"This gene encodes a protein which acts as a receptor for adiponectin, a hormone secreted by adipocytes which regulates fatty acid catabolism and glucose levels. Binding of adiponectin to the encoded protein results in activation of an AMP-activated kinase signaling pathway which affects levels of fatty acid oxidation and insulin sensitivity. A pseudogene of this gene is located on chromosome 14. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2014]","start":202940823,"end":202958572,"strand":-1,"description":"adiponectin receptor 1 [Source:HGNC Symbol;Acc:HGNC:24040]"}, {"versioned_ensembl_gene_id":"ENSG00000214915.3","gene_symbol":"BX546450.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151515551,"end":151516245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278849.1","gene_symbol":"AL513478.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66159954,"end":66179430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232457.4","gene_symbol":"SLC16A6P1","gene_name":"SLC16A6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48932]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440459","summary":null,"start":64953683,"end":64956546,"strand":1,"description":"SLC16A6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48932]"}, {"versioned_ensembl_gene_id":"ENSG00000254909.1","gene_symbol":"AP003392.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119005727,"end":119005934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169738.7","gene_symbol":"DCXR","gene_name":"dicarbonyl and L-xylulose reductase [Source:HGNC Symbol;Acc:HGNC:18985]","synonyms":"SDR20C1,KIDCR,DCR","biotype":"protein_coding","ncbi_id":"51181","summary":"The protein encoded by this gene acts as a homotetramer to catalyze diacetyl reductase and L-xylulose reductase reactions. The encoded protein may play a role in the uronate cycle of glucose metabolism and in the cellular osmoregulation in the proximal renal tubules. Defects in this gene are a cause of pentosuria. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]","start":82035136,"end":82037732,"strand":-1,"description":"dicarbonyl and L-xylulose reductase [Source:HGNC Symbol;Acc:HGNC:18985]"}, {"versioned_ensembl_gene_id":"ENSG00000258949.1","gene_symbol":"AL049870.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44898908,"end":44911863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226693.1","gene_symbol":"NXNP1","gene_name":"nucleoredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130251","summary":null,"start":218881600,"end":218882650,"strand":-1,"description":"nucleoredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50561]"}, {"versioned_ensembl_gene_id":"ENSG00000250655.1","gene_symbol":"AC096661.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96212279,"end":96213100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272396.1","gene_symbol":"AC005392.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43360685,"end":43368970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211885.1","gene_symbol":"TRAJ4","gene_name":"T-cell receptor alpha joining 4 [Source:HGNC Symbol;Acc:HGNC:12070]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28751","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22542199,"end":22542261,"strand":1,"description":"T-cell receptor alpha joining 4 [Source:HGNC Symbol;Acc:HGNC:12070]"}, {"versioned_ensembl_gene_id":"ENSG00000230826.1","gene_symbol":"AL390774.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123736437,"end":123751941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188761.11","gene_symbol":"BCL2L15","gene_name":"BCL2 like 15 [Source:HGNC Symbol;Acc:HGNC:33624]","synonyms":"Bfk,FLJ22588,C1orf178","biotype":"protein_coding","ncbi_id":"440603","summary":null,"start":113878168,"end":113887547,"strand":-1,"description":"BCL2 like 15 [Source:HGNC Symbol;Acc:HGNC:33624]"}, {"versioned_ensembl_gene_id":"ENSG00000259126.1","gene_symbol":"AL161752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44392531,"end":44393716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251586.1","gene_symbol":"TET2-AS1","gene_name":"TET2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104384744","summary":null,"start":105171354,"end":105178063,"strand":-1,"description":"TET2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41125]"}, {"versioned_ensembl_gene_id":"ENSG00000204685.6","gene_symbol":"STARD7-AS1","gene_name":"STARD7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40827]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285033","summary":null,"start":96208416,"end":96242621,"strand":1,"description":"STARD7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40827]"}, {"versioned_ensembl_gene_id":"ENSG00000106351.12","gene_symbol":"AGFG2","gene_name":"ArfGAP with FG repeats 2 [Source:HGNC Symbol;Acc:HGNC:5177]","synonyms":"RABR,HRBL","biotype":"protein_coding","ncbi_id":"3268","summary":"This gene is a member of the HIV-1 Rev binding protein (HRB) family and encodes a protein with one Arf-GAP zinc finger domain, several phe-gly (FG) motifs, and four asn-pro-phe (NPF) motifs. This protein interacts with Eps15 homology (EH) domains and plays a role in the Rev export pathway, which mediates the nucleocytoplasmic transfer of proteins and RNAs. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Feb 2013]","start":100539211,"end":100568219,"strand":1,"description":"ArfGAP with FG repeats 2 [Source:HGNC Symbol;Acc:HGNC:5177]"}, {"versioned_ensembl_gene_id":"ENSG00000214414.9","gene_symbol":"TRIM77","gene_name":"tripartite motif containing 77 [Source:HGNC Symbol;Acc:HGNC:34228]","synonyms":"TRIM77P","biotype":"protein_coding","ncbi_id":"390231","summary":null,"start":89710299,"end":89717872,"strand":1,"description":"tripartite motif containing 77 [Source:HGNC Symbol;Acc:HGNC:34228]"}, {"versioned_ensembl_gene_id":"ENSG00000259957.2","gene_symbol":"AC007614.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49294886,"end":49296736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211859.1","gene_symbol":"TRAJ30","gene_name":"T-cell receptor alpha joining 30 [Source:HGNC Symbol;Acc:HGNC:12060]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28725","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22512852,"end":22512908,"strand":1,"description":"T-cell receptor alpha joining 30 [Source:HGNC Symbol;Acc:HGNC:12060]"}, {"versioned_ensembl_gene_id":"ENSG00000228992.2","gene_symbol":"RPL5P32","gene_name":"ribosomal protein L5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271207","summary":null,"start":27895704,"end":27896582,"strand":1,"description":"ribosomal protein L5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36973]"}, {"versioned_ensembl_gene_id":"ENSG00000261421.1","gene_symbol":"AC044798.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49159508,"end":49162023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213026.4","gene_symbol":"CFL1P4","gene_name":"cofilin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1880]","synonyms":"CFLP4,CFLL4","biotype":"processed_pseudogene","ncbi_id":"645980","summary":null,"start":241993185,"end":241993682,"strand":1,"description":"cofilin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1880]"}, {"versioned_ensembl_gene_id":"ENSG00000256826.1","gene_symbol":"ATP5J2P4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32451]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654485","summary":null,"start":64491523,"end":64491789,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32451]"}, {"versioned_ensembl_gene_id":"ENSG00000273261.1","gene_symbol":"AC092953.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":182921240,"end":182921938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131242.17","gene_symbol":"RAB11FIP4","gene_name":"RAB11 family interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30267]","synonyms":"RAB11-FIP4,MGC11316,KIAA1821,FLJ00131","biotype":"protein_coding","ncbi_id":"84440","summary":"The protein encoded by this gene interacts with RAB11 and is thought to be involved in bringing recycling endosome membranes to the cleavage furrow in late cytokinesis. Hypoxic conditions can lead to an upregulation of the encoded protein and enhance the metastatic potential of hepatocellular carcinoma. [provided by RefSeq, Oct 2016]","start":31391624,"end":31538217,"strand":1,"description":"RAB11 family interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30267]"}, {"versioned_ensembl_gene_id":"ENSG00000230064.1","gene_symbol":"AL772161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133338990,"end":133339465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270729.1","gene_symbol":"AC004853.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143979121,"end":143980225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223870.1","gene_symbol":"AP000233.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25127469,"end":25135247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166337.9","gene_symbol":"TAF10","gene_name":"TATA-box binding protein associated factor 10 [Source:HGNC Symbol;Acc:HGNC:11543]","synonyms":"TAFII30,TAF2H,TAF2A","biotype":"protein_coding","ncbi_id":"6881","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the small subunits of TFIID that is associated with a subset of TFIID complexes. Studies with human and mammalian cells have shown that this subunit is required for transcriptional activation by the estrogen receptor, for progression through the cell cycle, and may also be required for certain cellular differentiation programs. [provided by RefSeq, Jul 2008]","start":6606296,"end":6612667,"strand":-1,"description":"TATA-box binding protein associated factor 10 [Source:HGNC Symbol;Acc:HGNC:11543]"}, {"versioned_ensembl_gene_id":"ENSG00000232445.1","gene_symbol":"AC006329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101308346,"end":101310985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232301.1","gene_symbol":"LNCPRESS1","gene_name":"lncRNA p53 regulated and ESC associated 1 [Source:HGNC Symbol;Acc:HGNC:52746]","synonyms":"lncPRESS1","biotype":"antisense_RNA","ncbi_id":"101927721","summary":null,"start":101299613,"end":101301270,"strand":1,"description":"lncRNA p53 regulated and ESC associated 1 [Source:HGNC Symbol;Acc:HGNC:52746]"}, {"versioned_ensembl_gene_id":"ENSG00000214655.10","gene_symbol":"ZSWIM8","gene_name":"zinc finger SWIM-type containing 8 [Source:HGNC Symbol;Acc:HGNC:23528]","synonyms":"KIAA0913,4832404P21Rik","biotype":"protein_coding","ncbi_id":"23053","summary":null,"start":73785582,"end":73801797,"strand":1,"description":"zinc finger SWIM-type containing 8 [Source:HGNC Symbol;Acc:HGNC:23528]"}, {"versioned_ensembl_gene_id":"ENSG00000233429.9","gene_symbol":"HOTAIRM1","gene_name":"HOXA transcript antisense RNA, myeloid-specific 1 [Source:HGNC Symbol;Acc:HGNC:37117]","synonyms":"NCRNA00179,HOXA1-AS1,HOXA-AS1","biotype":"antisense_RNA","ncbi_id":"100506311","summary":"This non-coding locus is located in the HOX gene cluster. Transcription of this locus is induced by retinoic acid, and transcripts likely function in regulation of myelopoiesis through transcriptional activation of several genes in the HOXA cluster, in addition to several beta-2 integrins. [provided by RefSeq, Jan 2013]","start":27095647,"end":27100265,"strand":1,"description":"HOXA transcript antisense RNA, myeloid-specific 1 [Source:HGNC Symbol;Acc:HGNC:37117]"}, {"versioned_ensembl_gene_id":"ENSG00000232184.1","gene_symbol":"AL662889.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":243702857,"end":243740821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236901.6","gene_symbol":"MIR600HG","gene_name":"MIR600 host gene [Source:HGNC Symbol;Acc:HGNC:23642]","synonyms":"NCRNA00287,GL012,FLJ22161,C9orf45","biotype":"sense_intronic","ncbi_id":"81571","summary":null,"start":123109494,"end":123115477,"strand":-1,"description":"MIR600 host gene [Source:HGNC Symbol;Acc:HGNC:23642]"}, {"versioned_ensembl_gene_id":"ENSG00000236013.5","gene_symbol":"AL138737.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140067435,"end":140093721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170525.19","gene_symbol":"PFKFB3","gene_name":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 [Source:HGNC Symbol;Acc:HGNC:8874]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5209","summary":"The protein encoded by this gene belongs to a family of bifunctional proteins that are involved in both the synthesis and degradation of fructose-2,6-bisphosphate, a regulatory molecule that controls glycolysis in eukaryotes. The encoded protein has a 6-phosphofructo-2-kinase activity that catalyzes the synthesis of fructose-2,6-bisphosphate (F2,6BP), and a fructose-2,6-biphosphatase activity that catalyzes the degradation of F2,6BP. This protein is required for cell cycle progression and prevention of apoptosis. It functions as a regulator of cyclin-dependent kinase 1, linking glucose metabolism to cell proliferation and survival in tumor cells. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2016]","start":6144934,"end":6254644,"strand":1,"description":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 [Source:HGNC Symbol;Acc:HGNC:8874]"}, {"versioned_ensembl_gene_id":"ENSG00000236655.1","gene_symbol":"AC023347.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126311466,"end":126311927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131711.14","gene_symbol":"MAP1B","gene_name":"microtubule associated protein 1B [Source:HGNC Symbol;Acc:HGNC:6836]","synonyms":"PPP1R102,MAP5","biotype":"protein_coding","ncbi_id":"4131","summary":"This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The product of this gene is a precursor polypeptide that presumably undergoes proteolytic processing to generate the final MAP1B heavy chain and LC1 light chain. Gene knockout studies of the mouse microtubule-associated protein 1B gene suggested an important role in development and function of the nervous system. [provided by RefSeq, Jul 2008]","start":72107234,"end":72209570,"strand":1,"description":"microtubule associated protein 1B [Source:HGNC Symbol;Acc:HGNC:6836]"}, {"versioned_ensembl_gene_id":"ENSG00000211848.1","gene_symbol":"TRAJ41","gene_name":"T-cell receptor alpha joining 41 [Source:HGNC Symbol;Acc:HGNC:12072]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28714","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22497657,"end":22497718,"strand":1,"description":"T-cell receptor alpha joining 41 [Source:HGNC Symbol;Acc:HGNC:12072]"}, {"versioned_ensembl_gene_id":"ENSG00000277235.1","gene_symbol":"AL035420.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36064243,"end":36064563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169594.13","gene_symbol":"BNC1","gene_name":"basonuclin 1 [Source:HGNC Symbol;Acc:HGNC:1081]","synonyms":"HsT19447,BNC","biotype":"protein_coding","ncbi_id":"646","summary":"This gene encodes a zinc finger protein present in the basal cell layer of the epidermis and in hair follicles. It is also found in abundance in the germ cells of testis and ovary. This protein is thought to play a regulatory role in keratinocyte proliferation and it may also be a regulator for rRNA transcription. Disruption of this gene has been implicated in premature ovarian failure as well as testicular premature aging. [provided by RefSeq, Sep 2020]","start":83255903,"end":83284714,"strand":-1,"description":"basonuclin 1 [Source:HGNC Symbol;Acc:HGNC:1081]"}, {"versioned_ensembl_gene_id":"ENSG00000228681.1","gene_symbol":"AC008072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224294930,"end":224295753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248864.1","gene_symbol":"AC114316.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92329230,"end":92332584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172340.14","gene_symbol":"SUCLG2","gene_name":"succinate-CoA ligase GDP-forming beta subunit [Source:HGNC Symbol;Acc:HGNC:11450]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8801","summary":"This gene encodes a GTP-specific beta subunit of succinyl-CoA synthetase. Succinyl-CoA synthetase catalyzes the reversible reaction involving the formation of succinyl-CoA and succinate. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 5 and 12. [provided by RefSeq, Apr 2010]","start":67360460,"end":67654614,"strand":-1,"description":"succinate-CoA ligase GDP-forming beta subunit [Source:HGNC Symbol;Acc:HGNC:11450]"}, {"versioned_ensembl_gene_id":"ENSG00000249873.6","gene_symbol":"LINC02372","gene_name":"long intergenic non-protein coding RNA 2372 [Source:HGNC Symbol;Acc:HGNC:53294]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440117","summary":null,"start":126869490,"end":126874690,"strand":-1,"description":"long intergenic non-protein coding RNA 2372 [Source:HGNC Symbol;Acc:HGNC:53294]"}, {"versioned_ensembl_gene_id":"ENSG00000163584.17","gene_symbol":"RPL22L1","gene_name":"ribosomal protein L22 like 1 [Source:HGNC Symbol;Acc:HGNC:27610]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200916","summary":null,"start":170864875,"end":170870483,"strand":-1,"description":"ribosomal protein L22 like 1 [Source:HGNC Symbol;Acc:HGNC:27610]"}, {"versioned_ensembl_gene_id":"ENSG00000233647.2","gene_symbol":"NENFP1","gene_name":"neudesin neurotrophic factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480294","summary":null,"start":46665910,"end":46666375,"strand":-1,"description":"neudesin neurotrophic factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50298]"}, {"versioned_ensembl_gene_id":"ENSG00000255329.1","gene_symbol":"H2AFZP4","gene_name":"H2A histone family member Z pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38015]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462795","summary":null,"start":70278921,"end":70279297,"strand":-1,"description":"H2A histone family member Z pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38015]"}, {"versioned_ensembl_gene_id":"ENSG00000263489.1","gene_symbol":"AC127029.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63972920,"end":63989422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182168.14","gene_symbol":"UNC5C","gene_name":"unc-5 netrin receptor C [Source:HGNC Symbol;Acc:HGNC:12569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8633","summary":"This gene product belongs to the UNC-5 family of netrin receptors. Netrins are secreted proteins that direct axon extension and cell migration during neural development. They are bifunctional proteins that act as attractants for some cell types and as repellents for others, and these opposite actions are thought to be mediated by two classes of receptors. The UNC-5 family of receptors mediate the repellent response to netrin; they are transmembrane proteins containing 2 immunoglobulin (Ig)-like domains and 2 type I thrombospondin motifs in the extracellular region. [provided by RefSeq, Jul 2008]","start":95162504,"end":95549206,"strand":-1,"description":"unc-5 netrin receptor C [Source:HGNC Symbol;Acc:HGNC:12569]"}, {"versioned_ensembl_gene_id":"ENSG00000225305.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"OTTHUMG00000086663,BPG126D10.10","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577561,"end":29577850,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000249482.1","gene_symbol":"USP17L14P","gene_name":"ubiquitin specific peptidase 17-like family member 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44442]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287270","summary":null,"start":9229641,"end":9231233,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44442]"}, {"versioned_ensembl_gene_id":"ENSG00000150457.8","gene_symbol":"LATS2","gene_name":"large tumor suppressor kinase 2 [Source:HGNC Symbol;Acc:HGNC:6515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26524","summary":"This gene encodes a serine/threonine protein kinase belonging to the LATS tumor suppressor family. The protein localizes to centrosomes during interphase, and early and late metaphase. It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis. It also interacts with a negative regulator of p53 and may function in a positive feedback loop with p53 that responds to cytoskeleton damage. Additionally, it can function as a co-repressor of androgen-responsive gene expression. [provided by RefSeq, Jul 2008]","start":20973032,"end":21061547,"strand":-1,"description":"large tumor suppressor kinase 2 [Source:HGNC Symbol;Acc:HGNC:6515]"}, {"versioned_ensembl_gene_id":"ENSG00000138136.6","gene_symbol":"LBX1","gene_name":"ladybird homeobox 1 [Source:HGNC Symbol;Acc:HGNC:16960]","synonyms":"LBX1H,HPX6","biotype":"protein_coding","ncbi_id":"10660","summary":"This gene and the orthologous mouse gene were found by their homology to the Drosophila lady bird early and late homeobox genes. In the mouse, this gene is a key regulator of muscle precursor cell migration and is required for the acquisition of dorsal identities of forelimb muscles. [provided by RefSeq, Jul 2008]","start":101226195,"end":101229794,"strand":-1,"description":"ladybird homeobox 1 [Source:HGNC Symbol;Acc:HGNC:16960]"}, {"versioned_ensembl_gene_id":"ENSG00000229649.1","gene_symbol":"AL133387.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101252821,"end":101263550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248592.7","gene_symbol":"TMEM110-MUSTN1","gene_name":"TMEM110-MUSTN1 readthrough [Source:HGNC Symbol;Acc:HGNC:38834]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526772","summary":"This locus represents naturally occurring read-through transcription between the neighboring TMEM110 (transmembrane protein 110) and MUSTN1 (musculoskeletal, embryonic nuclear protein 1) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":52833121,"end":52897562,"strand":-1,"description":"TMEM110-MUSTN1 readthrough [Source:HGNC Symbol;Acc:HGNC:38834]"}, {"versioned_ensembl_gene_id":"ENSG00000229656.6","gene_symbol":"AL365203.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32958845,"end":33082102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253124.1","gene_symbol":"TRAPPC2P2","gene_name":"trafficking protein particle complex 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10711]","synonyms":"SEDLP2","biotype":"processed_pseudogene","ncbi_id":"27196","summary":null,"start":71448811,"end":71449219,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10711]"}, {"versioned_ensembl_gene_id":"ENSG00000205022.9","gene_symbol":"PABPN1L","gene_name":"poly(A) binding protein nuclear 1 like, cytoplasmic [Source:HGNC Symbol;Acc:HGNC:37237]","synonyms":"ePABP2","biotype":"protein_coding","ncbi_id":"390748","summary":null,"start":88863333,"end":88866660,"strand":-1,"description":"poly(A) binding protein nuclear 1 like, cytoplasmic [Source:HGNC Symbol;Acc:HGNC:37237]"}, {"versioned_ensembl_gene_id":"ENSG00000092607.13","gene_symbol":"TBX15","gene_name":"T-box 15 [Source:HGNC Symbol;Acc:HGNC:11594]","synonyms":"TBX14","biotype":"protein_coding","ncbi_id":"6913","summary":"This gene belongs to the T-box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T-box DNA-binding domain. Mutations in this gene are associated with Cousin syndrome.[provided by RefSeq, Oct 2009]","start":118883046,"end":118989556,"strand":-1,"description":"T-box 15 [Source:HGNC Symbol;Acc:HGNC:11594]"}, {"versioned_ensembl_gene_id":"ENSG00000258431.1","gene_symbol":"AC004825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70858844,"end":70859429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260288.3","gene_symbol":"AC019294.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":75737820,"end":75763321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259213.1","gene_symbol":"AC105133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77787193,"end":77788674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118473.21","gene_symbol":"SGIP1","gene_name":"SH3 domain GRB2 like endophilin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:25412]","synonyms":"DKFZp761D221","biotype":"protein_coding","ncbi_id":"84251","summary":"SGIP1 functions as an endocytic protein that affects signaling by receptors in neuronal systems involved in energy homeostasis via its interaction with endophilins (see SH3GL3; MIM 603362) (Trevaskis et al., 2005 [PubMed 15919751] and Uezu et al., 2007 [PubMed 17626015]).[supplied by OMIM, Mar 2008]","start":66533383,"end":66748299,"strand":1,"description":"SH3 domain GRB2 like endophilin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:25412]"}, {"versioned_ensembl_gene_id":"ENSG00000231968.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555562,"end":29559875,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000144677.14","gene_symbol":"CTDSPL","gene_name":"CTD small phosphatase like [Source:HGNC Symbol;Acc:HGNC:16890]","synonyms":"SCP3,RBSP3,PSR1,HYA22,C3orf8","biotype":"protein_coding","ncbi_id":"10217","summary":null,"start":37861960,"end":37984469,"strand":1,"description":"CTD small phosphatase like [Source:HGNC Symbol;Acc:HGNC:16890]"}, {"versioned_ensembl_gene_id":"ENSG00000189367.14","gene_symbol":"KIAA0408","gene_name":"KIAA0408 [Source:HGNC Symbol;Acc:HGNC:21636]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9729","summary":null,"start":127440343,"end":127459391,"strand":-1,"description":"KIAA0408 [Source:HGNC Symbol;Acc:HGNC:21636]"}, {"versioned_ensembl_gene_id":"ENSG00000234019.1","gene_symbol":"AL591212.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53093710,"end":53094858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235901.2","gene_symbol":"AL442644.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102515204,"end":102518308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255171.5","gene_symbol":"LINC01499","gene_name":"long intergenic non-protein coding RNA 1499 [Source:HGNC Symbol;Acc:HGNC:51165]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723644","summary":null,"start":41714568,"end":41836442,"strand":1,"description":"long intergenic non-protein coding RNA 1499 [Source:HGNC Symbol;Acc:HGNC:51165]"}, {"versioned_ensembl_gene_id":"ENSG00000220694.2","gene_symbol":"AL096711.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127435636,"end":127436189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228740.2","gene_symbol":"GABRG3-AS1","gene_name":"GABRG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40249]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928869","summary":null,"start":27157615,"end":27161319,"strand":-1,"description":"GABRG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40249]"}, {"versioned_ensembl_gene_id":"ENSG00000211816.2","gene_symbol":"TRAV38-1","gene_name":"T-cell receptor alpha variable 38-1 [Source:HGNC Symbol;Acc:HGNC:12137]","synonyms":"TRAV381,TCRAV38S1,TCRAV14S2","biotype":"TR_V_gene","ncbi_id":"28644","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22271968,"end":22272563,"strand":1,"description":"T-cell receptor alpha variable 38-1 [Source:HGNC Symbol;Acc:HGNC:12137]"}, {"versioned_ensembl_gene_id":"ENSG00000198689.10","gene_symbol":"SLC9A6","gene_name":"solute carrier family 9 member A6 [Source:HGNC Symbol;Acc:HGNC:11079]","synonyms":"NHE6,KIAA0267","biotype":"protein_coding","ncbi_id":"10479","summary":"This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":135973841,"end":136047269,"strand":1,"description":"solute carrier family 9 member A6 [Source:HGNC Symbol;Acc:HGNC:11079]"}, {"versioned_ensembl_gene_id":"ENSG00000211815.3","gene_symbol":"TRAV36DV7","gene_name":"T-cell receptor alpha variable 36/delta variable 7 [Source:HGNC Symbol;Acc:HGNC:12135]","synonyms":"TRAV36/DV7","biotype":"TR_V_gene","ncbi_id":"28646","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22226746,"end":22227254,"strand":1,"description":"T-cell receptor alpha variable 36/delta variable 7 [Source:HGNC Symbol;Acc:HGNC:12135]"}, {"versioned_ensembl_gene_id":"ENSG00000255998.1","gene_symbol":"AC069235.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126690479,"end":126695832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167103.11","gene_symbol":"PIP5KL1","gene_name":"phosphatidylinositol-4-phosphate 5-kinase like 1 [Source:HGNC Symbol;Acc:HGNC:28711]","synonyms":"MGC46424,bA203J24.5","biotype":"protein_coding","ncbi_id":"138429","summary":"PIP5KL1 is a phosphoinositide kinase-like protein that lacks intrinsic lipid kinase activity but associates with type I PIPKs (see PIP5K1A; MIM 603275) and may play a role in localization of PIPK activity (Chang et al., 2004 [PubMed 14701839]).[supplied by OMIM, Jun 2009]","start":127920879,"end":127930797,"strand":-1,"description":"phosphatidylinositol-4-phosphate 5-kinase like 1 [Source:HGNC Symbol;Acc:HGNC:28711]"}, {"versioned_ensembl_gene_id":"ENSG00000234882.1","gene_symbol":"EIF3EP1","gene_name":"eukaryotic translation initiation factor 3 subunit E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6102]","synonyms":"INT6P1,EIF3S6P1,EIF3EP","biotype":"processed_pseudogene","ncbi_id":"3647","summary":null,"start":73291962,"end":73293277,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6102]"}, {"versioned_ensembl_gene_id":"ENSG00000068903.19","gene_symbol":"SIRT2","gene_name":"sirtuin 2 [Source:HGNC Symbol;Acc:HGNC:10886]","synonyms":"SIR2L","biotype":"protein_coding","ncbi_id":"22933","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Several transcript variants are resulted from alternative splicing of this gene. [provided by RefSeq, Jul 2010]","start":38878555,"end":38899862,"strand":-1,"description":"sirtuin 2 [Source:HGNC Symbol;Acc:HGNC:10886]"}, {"versioned_ensembl_gene_id":"ENSG00000254144.3","gene_symbol":"AC067930.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143542110,"end":143542400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259152.1","gene_symbol":"AC104002.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27422381,"end":27428338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256980.4","gene_symbol":"KHDC1L","gene_name":"KH domain containing 1 like [Source:HGNC Symbol;Acc:HGNC:37274]","synonyms":"RP11-257K9.7","biotype":"protein_coding","ncbi_id":"100129128","summary":null,"start":73223544,"end":73225770,"strand":-1,"description":"KH domain containing 1 like [Source:HGNC Symbol;Acc:HGNC:37274]"}, {"versioned_ensembl_gene_id":"ENSG00000258154.2","gene_symbol":"AL512356.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":105112690,"end":105112863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258689.1","gene_symbol":"LINC01269","gene_name":"long intergenic non-protein coding RNA 1269 [Source:HGNC Symbol;Acc:HGNC:50325]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103695436","summary":null,"start":70698698,"end":70712153,"strand":1,"description":"long intergenic non-protein coding RNA 1269 [Source:HGNC Symbol;Acc:HGNC:50325]"}, {"versioned_ensembl_gene_id":"ENSG00000282315.1","gene_symbol":"HNRNPA1P38","gene_name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421384","summary":null,"start":141464977,"end":141465933,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:48767]"}, {"versioned_ensembl_gene_id":"ENSG00000233688.1","gene_symbol":"BX842559.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154919578,"end":154920182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224260.6","gene_symbol":"AL023754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":209528455,"end":209567673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188386.6","gene_symbol":"PPP3R2","gene_name":"protein phosphatase 3 regulatory subunit B, beta [Source:HGNC Symbol;Acc:HGNC:9318]","synonyms":"PPP3RL","biotype":"protein_coding","ncbi_id":"5535","summary":null,"start":101591615,"end":101595021,"strand":-1,"description":"protein phosphatase 3 regulatory subunit B, beta [Source:HGNC Symbol;Acc:HGNC:9318]"}, {"versioned_ensembl_gene_id":"ENSG00000115641.18","gene_symbol":"FHL2","gene_name":"four and a half LIM domains 2 [Source:HGNC Symbol;Acc:HGNC:3703]","synonyms":"SLIM3,DRAL","biotype":"protein_coding","ncbi_id":"2274","summary":"This gene encodes a member of the four-and-a-half-LIM-only protein family. Family members contain two highly conserved, tandemly arranged, zinc finger domains with four highly conserved cysteines binding a zinc atom in each zinc finger. This protein is thought to have a role in the assembly of extracellular membranes. Also, this gene is down-regulated during transformation of normal myoblasts to rhabdomyosarcoma cells and the encoded protein may function as a link between presenilin-2 and an intracellular signaling pathway. Multiple alternatively spliced variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2016]","start":105357712,"end":105438513,"strand":-1,"description":"four and a half LIM domains 2 [Source:HGNC Symbol;Acc:HGNC:3703]"}, {"versioned_ensembl_gene_id":"ENSG00000058600.15","gene_symbol":"POLR3E","gene_name":"RNA polymerase III subunit E [Source:HGNC Symbol;Acc:HGNC:30347]","synonyms":"SIN,RPC5,FLJ10509","biotype":"protein_coding","ncbi_id":"55718","summary":null,"start":22297375,"end":22335103,"strand":1,"description":"RNA polymerase III subunit E [Source:HGNC Symbol;Acc:HGNC:30347]"}, {"versioned_ensembl_gene_id":"ENSG00000186047.9","gene_symbol":"DLEU7","gene_name":"deleted in lymphocytic leukemia, 7 [Source:HGNC Symbol;Acc:HGNC:17567]","synonyms":"FLJ44882","biotype":"protein_coding","ncbi_id":"220107","summary":null,"start":50711008,"end":50843939,"strand":-1,"description":"deleted in lymphocytic leukemia, 7 [Source:HGNC Symbol;Acc:HGNC:17567]"}, {"versioned_ensembl_gene_id":"ENSG00000197971.14","gene_symbol":"MBP","gene_name":"myelin basic protein [Source:HGNC Symbol;Acc:HGNC:6925]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4155","summary":"The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann cells in the nervous system. However, MBP-related transcripts are also present in the bone marrow and the immune system. These mRNAs arise from the long MBP gene (otherwise called \"Golli-MBP\") that contains 3 additional exons located upstream of the classic MBP exons. Alternative splicing from the Golli and the MBP transcription start sites gives rise to 2 sets of MBP-related transcripts and gene products. The Golli mRNAs contain 3 exons unique to Golli-MBP, spliced in-frame to 1 or more MBP exons. They encode hybrid proteins that have N-terminal Golli aa sequence linked to MBP aa sequence. The second family of transcripts contain only MBP exons and produce the well characterized myelin basic proteins. This complex gene structure is conserved among species suggesting that the MBP transcription unit is an integral part of the Golli transcription unit and that this arrangement is important for the function and/or regulation of these genes. [provided by RefSeq, Jul 2008]","start":76978827,"end":77133683,"strand":-1,"description":"myelin basic protein [Source:HGNC Symbol;Acc:HGNC:6925]"}, {"versioned_ensembl_gene_id":"ENSG00000261288.1","gene_symbol":"AC093525.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2554975,"end":2556105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277454.2","gene_symbol":"AC245078.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10845849,"end":11167832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135974.9","gene_symbol":"C2orf49","gene_name":"chromosome 2 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28772]","synonyms":"asw,MGC5509","biotype":"protein_coding","ncbi_id":"79074","summary":null,"start":105337359,"end":105349211,"strand":1,"description":"chromosome 2 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28772]"}, {"versioned_ensembl_gene_id":"ENSG00000274515.1","gene_symbol":"AC105020.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75645020,"end":75645442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280272.1","gene_symbol":"AC005858.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126141952,"end":126142377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174405.13","gene_symbol":"LIG4","gene_name":"DNA ligase 4 [Source:HGNC Symbol;Acc:HGNC:6601]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3981","summary":"The protein encoded by this gene is a DNA ligase that joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). This protein forms a complex with the X-ray repair cross complementing protein 4 (XRCC4), and further interacts with the DNA-dependent protein kinase (DNA-PK). Both XRCC4 and DNA-PK are known to be required for NHEJ. The crystal structure of the complex formed by this protein and XRCC4 has been resolved. Defects in this gene are the cause of LIG4 syndrome. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":108207439,"end":108218368,"strand":-1,"description":"DNA ligase 4 [Source:HGNC Symbol;Acc:HGNC:6601]"}, {"versioned_ensembl_gene_id":"ENSG00000203819.6","gene_symbol":"HIST2H2BC","gene_name":"histone cluster 2 H2B family member c (pseudogene) [Source:NCBI gene;Acc:337873]","synonyms":"HIST2H2BD,H2B/t","biotype":"processed_pseudogene","ncbi_id":"337873","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is found in a histone cluster on chromosome 1. [provided by RefSeq, Oct 2015]","start":149850193,"end":149850772,"strand":-1,"description":"histone cluster 2 H2B family member c (pseudogene) [Source:NCBI gene;Acc:337873]"}, {"versioned_ensembl_gene_id":"ENSG00000135966.12","gene_symbol":"TGFBRAP1","gene_name":"transforming growth factor beta receptor associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16836]","synonyms":"VPS3,TRAP1,TRAP-1","biotype":"protein_coding","ncbi_id":"9392","summary":"This gene encodes a protein that binds to transforming growth factor-beta (TGF-beta) receptors and plays a role in TGF-beta signaling. The encoded protein acts as a chaprone in signaling downstream of TGF-beta. It is involved in signal-dependent association with SMAD4. The protein is also a component of mammalian CORVET, a multisubunit tethering protein complex that is involved in fusion of early endosomes. [provided by RefSeq, Jun 2016]","start":105264391,"end":105330034,"strand":-1,"description":"transforming growth factor beta receptor associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16836]"}, {"versioned_ensembl_gene_id":"ENSG00000267408.1","gene_symbol":"AC011498.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4621194,"end":4622307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156113.22","gene_symbol":"KCNMA1","gene_name":"potassium calcium-activated channel subfamily M alpha 1 [Source:HGNC Symbol;Acc:HGNC:6284]","synonyms":"SLO,mSLO1,KCa1.1","biotype":"protein_coding","ncbi_id":"3778","summary":"MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit, which is the product of this gene, and the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":76869601,"end":77638369,"strand":-1,"description":"potassium calcium-activated channel subfamily M alpha 1 [Source:HGNC Symbol;Acc:HGNC:6284]"}, {"versioned_ensembl_gene_id":"ENSG00000274718.1","gene_symbol":"AL136964.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107870383,"end":107873372,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249207.1","gene_symbol":"AC079921.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39112677,"end":39126818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261094.2","gene_symbol":"AC007066.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":122937623,"end":122940333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272904.1","gene_symbol":"AL390726.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":38542479,"end":38568422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127743.5","gene_symbol":"IL17B","gene_name":"interleukin 17B [Source:HGNC Symbol;Acc:HGNC:5982]","synonyms":"MGC138901,MGC138900,IL-20,IL-17B,ZCYTO7,NIRF","biotype":"protein_coding","ncbi_id":"27190","summary":"The protein encoded by this gene is a T cell-derived cytokine that shares sequence similarity with IL17. This cytokine was reported to stimulate the release of TNF alpha (TNF) and IL1 beta (IL1B) from a monocytic cell line. Immunohistochemical analysis of several nerve tissues indicated that this cytokine is primarily localized to neuronal cell bodies. Alternative splicing results in multiple splice variants. [provided by RefSeq, Dec 2015]","start":149371324,"end":149404202,"strand":-1,"description":"interleukin 17B [Source:HGNC Symbol;Acc:HGNC:5982]"}, {"versioned_ensembl_gene_id":"ENSG00000249799.1","gene_symbol":"SNRPCP13","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49828]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481786","summary":null,"start":9583942,"end":9584131,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49828]"}, {"versioned_ensembl_gene_id":"ENSG00000249866.1","gene_symbol":"OR7E83P","gene_name":"olfactory receptor family 7 subfamily E member 83 pseudogene [Source:HGNC Symbol;Acc:HGNC:14688]","synonyms":"OR7E134P","biotype":"unprocessed_pseudogene","ncbi_id":"391630","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9512905,"end":9513874,"strand":1,"description":"olfactory receptor family 7 subfamily E member 83 pseudogene [Source:HGNC Symbol;Acc:HGNC:14688]"}, {"versioned_ensembl_gene_id":"ENSG00000268658.5","gene_symbol":"LINC00664","gene_name":"long intergenic non-protein coding RNA 664 [Source:HGNC Symbol;Acc:HGNC:44319]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400680","summary":null,"start":21483374,"end":21503238,"strand":1,"description":"long intergenic non-protein coding RNA 664 [Source:HGNC Symbol;Acc:HGNC:44319]"}, {"versioned_ensembl_gene_id":"ENSG00000168427.8","gene_symbol":"KLHL30","gene_name":"kelch like family member 30 [Source:HGNC Symbol;Acc:HGNC:24770]","synonyms":"FLJ43374","biotype":"protein_coding","ncbi_id":"377007","summary":null,"start":238138722,"end":238152947,"strand":1,"description":"kelch like family member 30 [Source:HGNC Symbol;Acc:HGNC:24770]"}, {"versioned_ensembl_gene_id":"ENSG00000275314.1","gene_symbol":"AC006924.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36794500,"end":36795460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248115.1","gene_symbol":"AC023154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52945649,"end":52958087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264885.1","gene_symbol":"AC026271.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18667629,"end":18669461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105467.8","gene_symbol":"SYNGR4","gene_name":"synaptogyrin 4 [Source:HGNC Symbol;Acc:HGNC:11502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23546","summary":"This gene encodes an integral membrane protein. The gene belongs to the synaptogyrin gene family. Like other members of the family the protein contains four transmembrane regions. The exact function of this protein is unclear. [provided by RefSeq, Jul 2008]","start":48364395,"end":48376376,"strand":1,"description":"synaptogyrin 4 [Source:HGNC Symbol;Acc:HGNC:11502]"}, {"versioned_ensembl_gene_id":"ENSG00000177084.16","gene_symbol":"POLE","gene_name":"DNA polymerase epsilon, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9177]","synonyms":"POLE1","biotype":"protein_coding","ncbi_id":"5426","summary":"This gene encodes the catalytic subunit of DNA polymerase epsilon. The enzyme is involved in DNA repair and chromosomal DNA replication. Mutations in this gene have been associated with colorectal cancer 12 and facial dysmorphism, immunodeficiency, livedo, and short stature. [provided by RefSeq, Sep 2013]","start":132623753,"end":132687365,"strand":-1,"description":"DNA polymerase epsilon, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9177]"}, {"versioned_ensembl_gene_id":"ENSG00000250231.1","gene_symbol":"USP17L16P","gene_name":"ubiquitin specific peptidase 17-like family member 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:44444]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287302","summary":null,"start":9239130,"end":9240722,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:44444]"}, {"versioned_ensembl_gene_id":"ENSG00000223989.1","gene_symbol":"AL357140.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9848318,"end":9850154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280398.1","gene_symbol":"AC005858.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126130166,"end":126130865,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108509.20","gene_symbol":"CAMTA2","gene_name":"calmodulin binding transcription activator 2 [Source:HGNC Symbol;Acc:HGNC:18807]","synonyms":"KIAA0909","biotype":"protein_coding","ncbi_id":"23125","summary":"The protein encoded by this gene is a member of the calmodulin-binding transcription activator protein family. Members of this family share a common domain structure that consists of a transcription activation domain, a DNA-binding domain, and a calmodulin-binding domain. The encoded protein may be a transcriptional coactivator of genes involved in cardiac growth. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jan 2010]","start":4967992,"end":4987652,"strand":-1,"description":"calmodulin binding transcription activator 2 [Source:HGNC Symbol;Acc:HGNC:18807]"}, {"versioned_ensembl_gene_id":"ENSG00000262728.5","gene_symbol":"AC123768.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32586105,"end":32615158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282625.1","gene_symbol":"AL121594.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35219023,"end":35219283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227134.1","gene_symbol":"AC093084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146477427,"end":146478113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260146.1","gene_symbol":"AC132186.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66450998,"end":66451351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239511.2","gene_symbol":"POM121L7P","gene_name":"POM121 transmembrane nucleoporin like 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:35444]","synonyms":"POM121L7","biotype":"processed_pseudogene","ncbi_id":"728418","summary":null,"start":21125660,"end":21128063,"strand":-1,"description":"POM121 transmembrane nucleoporin like 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:35444]"}, {"versioned_ensembl_gene_id":"ENSG00000253908.1","gene_symbol":"AC104115.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180257680,"end":180258366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232422.1","gene_symbol":"KNOP1P4","gene_name":"lysine rich nucleolar protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420843","summary":null,"start":72986313,"end":72987750,"strand":1,"description":"lysine rich nucleolar protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48922]"}, {"versioned_ensembl_gene_id":"ENSG00000273860.1","gene_symbol":"AC024581.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67855735,"end":67855986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077380.15","gene_symbol":"DYNC1I2","gene_name":"dynein cytoplasmic 1 intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:2964]","synonyms":"DNCI2,DIC74","biotype":"protein_coding","ncbi_id":"1781","summary":"This gene encodes a member of the dynein intermediate chain family. The encoded protein is a non-catalytic component of the cytoplasmic dynein 1 complex, which acts as a retrograde microtubule motor to transport organelles and vesicles. A pseudogene of this gene is located on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":171687409,"end":171748420,"strand":1,"description":"dynein cytoplasmic 1 intermediate chain 2 [Source:HGNC Symbol;Acc:HGNC:2964]"}, {"versioned_ensembl_gene_id":"ENSG00000225927.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"bA150A6.3,DDX6P,DDX6-Lp","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29329636,"end":29331071,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000267388.1","gene_symbol":"AF038458.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35960512,"end":35964063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225669.1","gene_symbol":"RPL23AP27","gene_name":"ribosomal protein L23a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36497]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271456","summary":null,"start":104678223,"end":104678673,"strand":1,"description":"ribosomal protein L23a pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36497]"}, {"versioned_ensembl_gene_id":"ENSG00000251206.1","gene_symbol":"AC010420.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67268022,"end":67270182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197210.7","gene_symbol":"AP000550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21114607,"end":21124451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279876.1","gene_symbol":"AC079248.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145874520,"end":145874845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135114.12","gene_symbol":"OASL","gene_name":"2'-5'-oligoadenylate synthetase like [Source:HGNC Symbol;Acc:HGNC:8090]","synonyms":"TRIP14,p59OASL","biotype":"protein_coding","ncbi_id":"8638","summary":null,"start":121019111,"end":121039242,"strand":-1,"description":"2'-5'-oligoadenylate synthetase like [Source:HGNC Symbol;Acc:HGNC:8090]"}, {"versioned_ensembl_gene_id":"ENSG00000197692.5","gene_symbol":"CBX3P7","gene_name":"chromobox 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42879]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421975","summary":null,"start":89293745,"end":89294246,"strand":-1,"description":"chromobox 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42879]"}, {"versioned_ensembl_gene_id":"ENSG00000154654.14","gene_symbol":"NCAM2","gene_name":"neural cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:7657]","synonyms":"NCAM21,MGC51008","biotype":"protein_coding","ncbi_id":"4685","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein and may function in selective fasciculation and zone-to-zone projection of the primary olfactory axons. [provided by RefSeq, Jul 2008]","start":20998315,"end":21543329,"strand":1,"description":"neural cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:7657]"}, {"versioned_ensembl_gene_id":"ENSG00000233093.5","gene_symbol":"LINC00892","gene_name":"long intergenic non-protein coding RNA 892 [Source:HGNC Symbol;Acc:HGNC:48578]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100128420","summary":null,"start":136639543,"end":136642429,"strand":1,"description":"long intergenic non-protein coding RNA 892 [Source:HGNC Symbol;Acc:HGNC:48578]"}, {"versioned_ensembl_gene_id":"ENSG00000166317.11","gene_symbol":"SYNPO2L","gene_name":"synaptopodin 2 like [Source:HGNC Symbol;Acc:HGNC:23532]","synonyms":"FLJ12921","biotype":"protein_coding","ncbi_id":"79933","summary":null,"start":73644881,"end":73663803,"strand":-1,"description":"synaptopodin 2 like [Source:HGNC Symbol;Acc:HGNC:23532]"}, {"versioned_ensembl_gene_id":"ENSG00000255082.1","gene_symbol":"GRM5-AS1","gene_name":"GRM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40265]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873989","summary":null,"start":88504576,"end":88524054,"strand":1,"description":"GRM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40265]"}, {"versioned_ensembl_gene_id":"ENSG00000280314.3","gene_symbol":"OR8K3","gene_name":"olfactory receptor family 8 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15313]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"219473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":56315144,"end":56320639,"strand":1,"description":"olfactory receptor family 8 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15313]"}, {"versioned_ensembl_gene_id":"ENSG00000250915.1","gene_symbol":"AC209005.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8745397,"end":8746033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235196.3","gene_symbol":"Z68868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101911529,"end":101912072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249086.1","gene_symbol":"AC051649.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":1864177,"end":1866667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230056.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"bA150A6.3,DDX6P,DDX6-Lp","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29329626,"end":29331061,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000234817.2","gene_symbol":"AL136309.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4136072,"end":4157385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263247.6","gene_symbol":"PRR4","gene_name":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]","synonyms":"PROL4,LPRP","biotype":"protein_coding","ncbi_id":"11272","summary":"This gene encodes a member of the proline-rich protein family that lacks a conserved repetitive domain. This protein may play a role in protective functions in the eye. Alternative splicing result in multiple transcript variants. Read-through transcription also exists between this gene and the upstream PRH1 (proline-rich protein HaeIII subfamily 1) gene. [provided by RefSeq, Feb 2011]","start":10824960,"end":11203561,"strand":-1,"description":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]"}, {"versioned_ensembl_gene_id":"ENSG00000073712.14","gene_symbol":"FERMT2","gene_name":"fermitin family member 2 [Source:HGNC Symbol;Acc:HGNC:15767]","synonyms":"UNC112B,PLEKHC1,mig-2,KIND2","biotype":"protein_coding","ncbi_id":"10979","summary":null,"start":52857268,"end":52952435,"strand":-1,"description":"fermitin family member 2 [Source:HGNC Symbol;Acc:HGNC:15767]"}, {"versioned_ensembl_gene_id":"ENSG00000228372.7","gene_symbol":"SMIM10L2B-AS1","gene_name":"SMIM10L2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53137]","synonyms":"ENST00000453528","biotype":"lincRNA","ncbi_id":"100287728","summary":null,"start":135059685,"end":135123952,"strand":1,"description":"SMIM10L2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53137]"}, {"versioned_ensembl_gene_id":"ENSG00000117362.12","gene_symbol":"APH1A","gene_name":"aph-1 homolog A, gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:29509]","synonyms":"CGI-78,APH-1A","biotype":"protein_coding","ncbi_id":"51107","summary":"This gene encodes a component of the gamma secretase complex that cleaves integral membrane proteins such as Notch receptors and beta-amyloid precursor protein. The gamma secretase complex contains this gene product, or the paralogous anterior pharynx defective 1 homolog B (APH1B), along with the presenilin, nicastrin, and presenilin enhancer-2 proteins. The precise function of this seven-transmembrane-domain protein is unknown though it is suspected of facilitating the association of nicastrin and presenilin in the gamma secretase complex as well as interacting with substrates of the gamma secretase complex prior to their proteolytic processing. Polymorphisms in a promoter region of this gene have been associated with an increased risk for developing sporadic Alzheimer's disease. Alternative splicing results in multiple protein-coding and non-protein-coding transcript variants. [provided by RefSeq, Aug 2011]","start":150265399,"end":150269580,"strand":-1,"description":"aph-1 homolog A, gamma-secretase subunit [Source:HGNC Symbol;Acc:HGNC:29509]"}, {"versioned_ensembl_gene_id":"ENSG00000213911.2","gene_symbol":"AL645937.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229227,"end":29230157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258999.1","gene_symbol":"AL136040.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81107033,"end":81170414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224924.6","gene_symbol":"LINC00320","gene_name":"long intergenic non-protein coding RNA 320 [Source:HGNC Symbol;Acc:HGNC:19690]","synonyms":"PRED14,NCRNA00320,FLJ37539,C21orf131","biotype":"lincRNA","ncbi_id":"387486","summary":null,"start":20742590,"end":20803216,"strand":-1,"description":"long intergenic non-protein coding RNA 320 [Source:HGNC Symbol;Acc:HGNC:19690]"}, {"versioned_ensembl_gene_id":"ENSG00000242524.1","gene_symbol":"AL672167.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29268462,"end":29269421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165995.18","gene_symbol":"CACNB2","gene_name":"calcium voltage-gated channel auxiliary subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:1402]","synonyms":"MYSB,CACNLB2","biotype":"protein_coding","ncbi_id":"783","summary":"This gene encodes a subunit of a voltage-dependent calcium channel protein that is a member of the voltage-gated calcium channel superfamily. The gene product was originally identified as an antigen target in Lambert-Eaton myasthenic syndrome, an autoimmune disorder. Mutations in this gene are associated with Brugada syndrome. Alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Feb 2013]","start":18140677,"end":18541869,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:1402]"}, {"versioned_ensembl_gene_id":"ENSG00000231041.1","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"dJ25J6.5,C6orf100","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28943846,"end":28944506,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000224006.1","gene_symbol":"AL645935.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29995625,"end":29996628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176018.12","gene_symbol":"LYSMD3","gene_name":"LysM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26969]","synonyms":"FLJ13542","biotype":"protein_coding","ncbi_id":"116068","summary":null,"start":90515611,"end":90529584,"strand":-1,"description":"LysM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26969]"}, {"versioned_ensembl_gene_id":"ENSG00000249514.1","gene_symbol":"TMEM251P1","gene_name":"transmembrane protein 251 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52396]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420909","summary":null,"start":91030990,"end":91031307,"strand":-1,"description":"transmembrane protein 251 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52396]"}, {"versioned_ensembl_gene_id":"ENSG00000241097.2","gene_symbol":"AP001324.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74738478,"end":74738796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121270.15","gene_symbol":"ABCC11","gene_name":"ATP binding cassette subfamily C member 11 [Source:HGNC Symbol;Acc:HGNC:14639]","synonyms":"MRP8","biotype":"protein_coding","ncbi_id":"85320","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This ABC full transporter is a member of the MRP subfamily which is involved in multi-drug resistance. The product of this gene participates in physiological processes involving bile acids, conjugated steroids, and cyclic nucleotides. In addition, a SNP in this gene is responsible for determination of human earwax type. This gene and family member ABCC12 are determined to be derived by duplication and are both localized to chromosome 16q12.1. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jul 2008]","start":48166910,"end":48247568,"strand":-1,"description":"ATP binding cassette subfamily C member 11 [Source:HGNC Symbol;Acc:HGNC:14639]"}, {"versioned_ensembl_gene_id":"ENSG00000236283.4","gene_symbol":"AC019197.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":164840672,"end":165208261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000002822.15","gene_symbol":"MAD1L1","gene_name":"MAD1 mitotic arrest deficient like 1 [Source:HGNC Symbol;Acc:HGNC:6762]","synonyms":"PIG9,MAD1,HsMAD1,TXBP181,TP53I9","biotype":"protein_coding","ncbi_id":"8379","summary":"MAD1L1 is a component of the mitotic spindle-assembly checkpoint that prevents the onset of anaphase until all chromosome are properly aligned at the metaphase plate. MAD1L1 functions as a homodimer and interacts with MAD2L1. MAD1L1 may play a role in cell cycle control and tumor suppression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":1815793,"end":2233243,"strand":-1,"description":"MAD1 mitotic arrest deficient like 1 [Source:HGNC Symbol;Acc:HGNC:6762]"}, {"versioned_ensembl_gene_id":"ENSG00000272751.1","gene_symbol":"AC006518.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10894943,"end":10895882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263158.1","gene_symbol":"AC018630.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11048332,"end":11049256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230198.1","gene_symbol":"RPL37P4","gene_name":"ribosomal protein L37 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:17239]","synonyms":"RL37P2","biotype":"processed_pseudogene","ncbi_id":"378819","summary":null,"start":19593841,"end":19594108,"strand":1,"description":"ribosomal protein L37 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:17239]"}, {"versioned_ensembl_gene_id":"ENSG00000185638.9","gene_symbol":"FTH1P14","gene_name":"ferritin heavy chain 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39090]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139431","summary":null,"start":34147036,"end":34147586,"strand":1,"description":"ferritin heavy chain 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39090]"}, {"versioned_ensembl_gene_id":"ENSG00000146453.12","gene_symbol":"PNLDC1","gene_name":"PARN like, ribonuclease domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21185]","synonyms":"FLJ40240,dJ195P10.2","biotype":"protein_coding","ncbi_id":"154197","summary":null,"start":159800249,"end":159820704,"strand":1,"description":"PARN like, ribonuclease domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21185]"}, {"versioned_ensembl_gene_id":"ENSG00000271078.1","gene_symbol":"AC139426.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32250302,"end":32256125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267369.1","gene_symbol":"AC015911.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35498218,"end":35499175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176253.3","gene_symbol":"OR4K13","gene_name":"olfactory receptor family 4 subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:15351]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390433","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20029399,"end":20036038,"strand":-1,"description":"olfactory receptor family 4 subfamily K member 13 [Source:HGNC Symbol;Acc:HGNC:15351]"}, {"versioned_ensembl_gene_id":"ENSG00000227586.5","gene_symbol":"RPS26P39","gene_name":"ribosomal protein S26 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36958]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128168","summary":null,"start":123171535,"end":123171875,"strand":-1,"description":"ribosomal protein S26 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36958]"}, {"versioned_ensembl_gene_id":"ENSG00000141294.9","gene_symbol":"LRRC46","gene_name":"leucine rich repeat containing 46 [Source:HGNC Symbol;Acc:HGNC:25047]","synonyms":"MGC16309","biotype":"protein_coding","ncbi_id":"90506","summary":null,"start":47831627,"end":47837713,"strand":1,"description":"leucine rich repeat containing 46 [Source:HGNC Symbol;Acc:HGNC:25047]"}, {"versioned_ensembl_gene_id":"ENSG00000233648.1","gene_symbol":"AC010095.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108694750,"end":108694893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184741.6","gene_symbol":"OR5AQ1P","gene_name":"olfactory receptor family 5 subfamily AQ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15259]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81221","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56049785,"end":56055730,"strand":1,"description":"olfactory receptor family 5 subfamily AQ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15259]"}, {"versioned_ensembl_gene_id":"ENSG00000255246.1","gene_symbol":"AP000793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82603743,"end":82643419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262111.3","gene_symbol":"TAS2R30","gene_name":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]","synonyms":"T2R30,TAS2R47","biotype":"protein_coding","ncbi_id":"259293","summary":null,"start":11164906,"end":11166592,"strand":-1,"description":"taste 2 receptor member 30 [Source:HGNC Symbol;Acc:HGNC:19112]"}, {"versioned_ensembl_gene_id":"ENSG00000236387.1","gene_symbol":"AL139350.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4431161,"end":4431673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166359.10","gene_symbol":"WDR88","gene_name":"WD repeat domain 88 [Source:HGNC Symbol;Acc:HGNC:26999]","synonyms":"PQWD","biotype":"protein_coding","ncbi_id":"126248","summary":null,"start":33132090,"end":33175795,"strand":1,"description":"WD repeat domain 88 [Source:HGNC Symbol;Acc:HGNC:26999]"}, {"versioned_ensembl_gene_id":"ENSG00000251349.3","gene_symbol":"MSANTD3-TMEFF1","gene_name":"MSANTD3-TMEFF1 readthrough [Source:HGNC Symbol;Acc:HGNC:38838]","synonyms":"C9orf30-TMEFF1","biotype":"protein_coding","ncbi_id":"100526694","summary":"This locus represents naturally occurring read-through transcription from the neighboring MSANTD3 (Myb/SANT-like DNA-binding domain containing 3) and TMEFF1 (transmembrane protein with EGF-like and two follistatin-like domains 1) genes. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Aug 2013]","start":100442271,"end":100577636,"strand":1,"description":"MSANTD3-TMEFF1 readthrough [Source:HGNC Symbol;Acc:HGNC:38838]"}, {"versioned_ensembl_gene_id":"ENSG00000232011.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29946103,"end":29948077,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000141934.9","gene_symbol":"PLPP2","gene_name":"phospholipid phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:9230]","synonyms":"PPAP2C,PAP-2c,LPP2","biotype":"protein_coding","ncbi_id":"8612","summary":"The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. This protein is similar to phosphatidic acid phosphatase type 2A (PPAP2A) and type 2B (PPAP2B). All three proteins contain 6 transmembrane regions, and a consensus N-glycosylation site. This protein has been shown to possess membrane associated PAP activity. Three alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":281040,"end":291504,"strand":-1,"description":"phospholipid phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:9230]"}, {"versioned_ensembl_gene_id":"ENSG00000137193.13","gene_symbol":"PIM1","gene_name":"Pim-1 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:8986]","synonyms":"PIM","biotype":"protein_coding","ncbi_id":"5292","summary":"The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and PIM subfamily. This gene is expressed primarily in B-lymphoid and myeloid cell lines, and is overexpressed in hematopoietic malignancies and in prostate cancer. It plays a role in signal transduction in blood cells, contributing to both cell proliferation and survival, and thus provides a selective advantage in tumorigenesis. Both the human and orthologous mouse genes have been reported to encode two isoforms (with preferential cellular localization) resulting from the use of alternative in-frame translation initiation codons, the upstream non-AUG (CUG) and downstream AUG codons (PMIDs:16186805, 1825810).[provided by RefSeq, Aug 2011]","start":37170203,"end":37175426,"strand":1,"description":"Pim-1 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:8986]"}, {"versioned_ensembl_gene_id":"ENSG00000231408.8","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31611502,"end":31613772,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000273086.1","gene_symbol":"TAS2R9","gene_name":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]","synonyms":"TRB6,T2R9","biotype":"protein_coding","ncbi_id":"50835","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10809137,"end":10810168,"strand":-1,"description":"taste 2 receptor member 9 [Source:HGNC Symbol;Acc:HGNC:14917]"}, {"versioned_ensembl_gene_id":"ENSG00000217566.2","gene_symbol":"TDGF1P4","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11704]","synonyms":"TDGF4,CRIPTO-4,CR-4","biotype":"processed_pseudogene","ncbi_id":"22815","summary":null,"start":3941282,"end":3941801,"strand":1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:11704]"}, {"versioned_ensembl_gene_id":"ENSG00000261542.1","gene_symbol":"AC011978.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63215981,"end":63218034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225346.1","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29785655,"end":29786629,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000284543.1","gene_symbol":"LINC01226","gene_name":"long intergenic non-protein coding RNA 1226 [Source:HGNC Symbol;Acc:HGNC:49678]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"284551","summary":null,"start":31506226,"end":31583306,"strand":1,"description":"long intergenic non-protein coding RNA 1226 [Source:HGNC Symbol;Acc:HGNC:49678]"}, {"versioned_ensembl_gene_id":"ENSG00000264880.1","gene_symbol":"AP005901.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15159724,"end":15164467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284060.1","gene_symbol":"AC002472.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21002895,"end":21009453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100417.11","gene_symbol":"PMM1","gene_name":"phosphomannomutase 1 [Source:HGNC Symbol;Acc:HGNC:9114]","synonyms":"Sec53","biotype":"protein_coding","ncbi_id":"5372","summary":"Phosphomannomutase catalyzes the conversion between D-mannose 6-phosphate and D-mannose 1-phosphate which is a substrate for GDP-mannose synthesis. GDP-mannose is used for synthesis of dolichol-phosphate-mannose, which is essential for N-linked glycosylation and thus the secretion of several glycoproteins as well as for the synthesis of glycosyl-phosphatidyl-inositol (GPI) anchored proteins. [provided by RefSeq, Jul 2008]","start":41576894,"end":41589890,"strand":-1,"description":"phosphomannomutase 1 [Source:HGNC Symbol;Acc:HGNC:9114]"}, {"versioned_ensembl_gene_id":"ENSG00000267132.1","gene_symbol":"AC067852.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42648178,"end":42648738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021645.18","gene_symbol":"NRXN3","gene_name":"neurexin 3 [Source:HGNC Symbol;Acc:HGNC:8010]","synonyms":"KIAA0743,C14orf60","biotype":"protein_coding","ncbi_id":"9369","summary":"This gene encodes a member of a family of proteins that function in the nervous system as receptors and cell adhesion molecules. Extensive alternative splicing and the use of alternative promoters results in multiple transcript variants and protein isoforms for this gene, but the full-length nature of many of these variants has not been determined. Transcripts that initiate from an upstream promoter encode alpha isoforms, which contain epidermal growth factor-like (EGF-like) sequences and laminin G domains. Transcripts initiating from the downstream promoter encode beta isoforms, which lack EGF-like sequences. Genetic variation at this locus has been associated with a range of behavioral phenotypes, including alcohol dependence and autism spectrum disorder. [provided by RefSeq, Dec 2012]","start":78170373,"end":79868290,"strand":1,"description":"neurexin 3 [Source:HGNC Symbol;Acc:HGNC:8010]"}, {"versioned_ensembl_gene_id":"ENSG00000277782.1","gene_symbol":"AC068870.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80999593,"end":80999981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258723.1","gene_symbol":"AF099810.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78279572,"end":78283376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226770.1","gene_symbol":"AC000124.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127476883,"end":127485804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125901.5","gene_symbol":"MRPS26","gene_name":"mitochondrial ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:14045]","synonyms":"RPMS13,MRP-S26,MRP-S13,dJ534B8.3,C20orf193","biotype":"protein_coding","ncbi_id":"64949","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. This gene lies adjacent to and downstream of the gonadotropin-releasing hormone precursor gene. [provided by RefSeq, Jul 2008]","start":3045945,"end":3048254,"strand":1,"description":"mitochondrial ribosomal protein S26 [Source:HGNC Symbol;Acc:HGNC:14045]"}, {"versioned_ensembl_gene_id":"ENSG00000228295.1","gene_symbol":"LINC00392","gene_name":"long intergenic non-protein coding RNA 392 [Source:HGNC Symbol;Acc:HGNC:42720]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874155","summary":null,"start":73564244,"end":73588070,"strand":1,"description":"long intergenic non-protein coding RNA 392 [Source:HGNC Symbol;Acc:HGNC:42720]"}, {"versioned_ensembl_gene_id":"ENSG00000229708.1","gene_symbol":"MARK2P12","gene_name":"microtubule affinity regulating kinase 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421565","summary":null,"start":73407768,"end":73408352,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39803]"}, {"versioned_ensembl_gene_id":"ENSG00000225551.1","gene_symbol":"AL157827.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92539053,"end":92539184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251642.1","gene_symbol":"AC098680.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38286994,"end":38287491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127080.9","gene_symbol":"IPPK","gene_name":"inositol-pentakisphosphate 2-kinase [Source:HGNC Symbol;Acc:HGNC:14645]","synonyms":"INSP5K2,FLJ13163,C9orf12,IPK1,IP5K","biotype":"protein_coding","ncbi_id":"64768","summary":"The protein encoded by this gene is a kinase that phosphorylates position 2 of inositol-1,3,4,5,6-pentakisphosphate to form inositol-1,2,3,4,5,6-hexakisphosphate (InsP6). InsP6 has a variety of functions, including stimulation of DNA repair, endocytosis, and mRNA export. [provided by RefSeq, Nov 2010]","start":92613184,"end":92670265,"strand":-1,"description":"inositol-pentakisphosphate 2-kinase [Source:HGNC Symbol;Acc:HGNC:14645]"}, {"versioned_ensembl_gene_id":"ENSG00000237711.1","gene_symbol":"MTCO3P11","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52041]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075153","summary":null,"start":5100236,"end":5101009,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:52041]"}, {"versioned_ensembl_gene_id":"ENSG00000183888.4","gene_symbol":"C1orf64","gene_name":"chromosome 1 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:28339]","synonyms":"MGC24047,ERRF","biotype":"protein_coding","ncbi_id":"149563","summary":null,"start":16004236,"end":16008807,"strand":1,"description":"chromosome 1 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:28339]"}, {"versioned_ensembl_gene_id":"ENSG00000279761.2","gene_symbol":"OR5D13","gene_name":"olfactory receptor family 5 subfamily D member 13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15280]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390142","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":55773438,"end":55774382,"strand":1,"description":"olfactory receptor family 5 subfamily D member 13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15280]"}, {"versioned_ensembl_gene_id":"ENSG00000279227.1","gene_symbol":"AC009303.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":118014174,"end":118015673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147010.17","gene_symbol":"SH3KBP1","gene_name":"SH3 domain containing kinase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13867]","synonyms":"CIN85","biotype":"protein_coding","ncbi_id":"30011","summary":"This gene encodes an adapter protein that contains one or more N-terminal Src homology domains, a proline rich region and a C-terminal coiled-coil domain. The encoded protein facilitates protein-protein interactions and has been implicated in numerous cellular processes including apoptosis, cytoskeletal rearrangement, cell adhesion and in the regulation of clathrin-dependent endocytosis. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]","start":19533975,"end":19887601,"strand":-1,"description":"SH3 domain containing kinase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13867]"}, {"versioned_ensembl_gene_id":"ENSG00000232945.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"hs6M1-6,dJ80I19.4,OR6-8","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173317,"end":29174588,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000227311.3","gene_symbol":"AL031985.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40333078,"end":40333557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277959.1","gene_symbol":"AL162274.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131971202,"end":131971533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236771.2","gene_symbol":"CR388415.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137885,"end":29138821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261832.6","gene_symbol":"AC138894.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28456371,"end":28492098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264116.4","gene_symbol":"AC116003.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75407012,"end":75419040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241204.1","gene_symbol":"AC022730.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70424125,"end":70424576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276375.1","gene_symbol":"AL157712.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130282445,"end":130286604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229866.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29111900,"end":29112835,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000232931.5","gene_symbol":"LINC00342","gene_name":"long intergenic non-protein coding RNA 342 [Source:HGNC Symbol;Acc:HGNC:42470]","synonyms":"NCRNA00342","biotype":"lincRNA","ncbi_id":"150759","summary":null,"start":95807118,"end":95816215,"strand":-1,"description":"long intergenic non-protein coding RNA 342 [Source:HGNC Symbol;Acc:HGNC:42470]"}, {"versioned_ensembl_gene_id":"ENSG00000225736.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR2B3P,OR6-4","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086315,"end":29087321,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000070915.9","gene_symbol":"SLC12A3","gene_name":"solute carrier family 12 member 3 [Source:HGNC Symbol;Acc:HGNC:10912]","synonyms":"NCCT","biotype":"protein_coding","ncbi_id":"6559","summary":"This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56865207,"end":56915850,"strand":1,"description":"solute carrier family 12 member 3 [Source:HGNC Symbol;Acc:HGNC:10912]"}, {"versioned_ensembl_gene_id":"ENSG00000255554.1","gene_symbol":"OR7E1P","gene_name":"olfactory receptor family 7 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8391]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"341128","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":67974286,"end":67975243,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8391]"}, {"versioned_ensembl_gene_id":"ENSG00000213689.11","gene_symbol":"TREX1","gene_name":"three prime repair exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:12269]","synonyms":"DRN3,AGS1","biotype":"protein_coding","ncbi_id":"11277","summary":"This gene encodes a nuclear protein with 3' exonuclease activity. The encoded protein may play a role in DNA repair and serve as a proofreading function for DNA polymerase. Mutations in this gene result in Aicardi-Goutieres syndrome, chilblain lupus, Cree encephalitis, and other diseases of the immune system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":48465811,"end":48467645,"strand":1,"description":"three prime repair exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:12269]"}, {"versioned_ensembl_gene_id":"ENSG00000255230.1","gene_symbol":"AC004923.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67965873,"end":67966227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140740.10","gene_symbol":"UQCRC2","gene_name":"ubiquinol-cytochrome c reductase core protein II [Source:HGNC Symbol;Acc:HGNC:12586]","synonyms":"UQCR2,QCR2","biotype":"protein_coding","ncbi_id":"7385","summary":"The protein encoded by this gene is located in the mitochondrion, where it is part of the ubiquinol-cytochrome c reductase complex (also known as complex III). This complex constitutes a part of the mitochondrial respiratory chain. Defects in this gene are a cause of mitochondrial complex III deficiency nuclear type 5. [provided by RefSeq, Jul 2015]","start":21952660,"end":21983660,"strand":1,"description":"ubiquinol-cytochrome c reductase core protein II [Source:HGNC Symbol;Acc:HGNC:12586]"}, {"versioned_ensembl_gene_id":"ENSG00000185803.8","gene_symbol":"SLC52A2","gene_name":"solute carrier family 52 member 2 [Source:HGNC Symbol;Acc:HGNC:30224]","synonyms":"PAR1,hRFT3,GPR172A,GPCR41,FLJ11856,D15Ertd747e,RFVT2","biotype":"protein_coding","ncbi_id":"79581","summary":"This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012]","start":144354135,"end":144361272,"strand":1,"description":"solute carrier family 52 member 2 [Source:HGNC Symbol;Acc:HGNC:30224]"}, {"versioned_ensembl_gene_id":"ENSG00000238172.2","gene_symbol":"RPS2P35","gene_name":"ribosomal protein S2 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36757]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130980","summary":null,"start":100116755,"end":100117651,"strand":-1,"description":"ribosomal protein S2 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36757]"}, {"versioned_ensembl_gene_id":"ENSG00000271524.1","gene_symbol":"BNIP3P17","gene_name":"BCL2 interacting protein 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421704","summary":null,"start":20221869,"end":20222463,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49697]"}, {"versioned_ensembl_gene_id":"ENSG00000213988.10","gene_symbol":"ZNF90","gene_name":"zinc finger protein 90 [Source:HGNC Symbol;Acc:HGNC:13165]","synonyms":"HTF9","biotype":"protein_coding","ncbi_id":"7643","summary":null,"start":20077994,"end":20127076,"strand":1,"description":"zinc finger protein 90 [Source:HGNC Symbol;Acc:HGNC:13165]"}, {"versioned_ensembl_gene_id":"ENSG00000134590.13","gene_symbol":"RTL8C","gene_name":"retrotransposon Gag like 8C [Source:HGNC Symbol;Acc:HGNC:2569]","synonyms":"SIRH5,Mart8,MAR8C,Mar8,FAM127A,CXX1","biotype":"protein_coding","ncbi_id":"8933","summary":null,"start":135032366,"end":135033546,"strand":1,"description":"retrotransposon Gag like 8C [Source:HGNC Symbol;Acc:HGNC:2569]"}, {"versioned_ensembl_gene_id":"ENSG00000249834.3","gene_symbol":"PGBD4P3","gene_name":"piggyBac transposable element derived 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421136","summary":null,"start":148307298,"end":148308258,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44068]"}, {"versioned_ensembl_gene_id":"ENSG00000231951.1","gene_symbol":"AC004837.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39609610,"end":39610290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236015.1","gene_symbol":"AC011290.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39569376,"end":39570198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265340.1","gene_symbol":"OR4K7P","gene_name":"olfactory receptor family 4 subfamily K member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14756]","synonyms":"OR4K10P","biotype":"unprocessed_pseudogene","ncbi_id":"79306","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14570844,"end":14571788,"strand":1,"description":"olfactory receptor family 4 subfamily K member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14756]"}, {"versioned_ensembl_gene_id":"ENSG00000274307.1","gene_symbol":"AC023449.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25708470,"end":25710869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226122.1","gene_symbol":"DDC-AS1","gene_name":"DDC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40171]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129427","summary":null,"start":50531759,"end":50543463,"strand":1,"description":"DDC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40171]"}, {"versioned_ensembl_gene_id":"ENSG00000145248.6","gene_symbol":"SLC10A4","gene_name":"solute carrier family 10 member 4 [Source:HGNC Symbol;Acc:HGNC:22980]","synonyms":"MGC29802","biotype":"protein_coding","ncbi_id":"201780","summary":null,"start":48483343,"end":48489196,"strand":1,"description":"solute carrier family 10 member 4 [Source:HGNC Symbol;Acc:HGNC:22980]"}, {"versioned_ensembl_gene_id":"ENSG00000254461.1","gene_symbol":"AP001107.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66259567,"end":66261834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213860.4","gene_symbol":"RPL21P75","gene_name":"ribosomal protein L21 pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:36460]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728501","summary":null,"start":20002765,"end":20003247,"strand":1,"description":"ribosomal protein L21 pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:36460]"}, {"versioned_ensembl_gene_id":"ENSG00000253900.1","gene_symbol":"CDH12P4","gene_name":"cadherin 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37700]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100093626","summary":null,"start":71132993,"end":71133287,"strand":1,"description":"cadherin 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37700]"}, {"versioned_ensembl_gene_id":"ENSG00000253577.1","gene_symbol":"AC104211.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92765702,"end":92776451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229044.1","gene_symbol":"AL451070.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31333067,"end":31346799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269321.1","gene_symbol":"AC011466.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48145908,"end":48147413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274867.1","gene_symbol":"AL589994.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49115537,"end":49116115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275164.3","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195747176,"end":195811179,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000218337.1","gene_symbol":"AL589994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49077712,"end":49078051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255440.1","gene_symbol":"AP001085.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74409060,"end":74416379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187589.8","gene_symbol":"TERF1P2","gene_name":"telomeric repeat binding factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38110]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646359","summary":null,"start":14377546,"end":14378757,"strand":-1,"description":"telomeric repeat binding factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38110]"}, {"versioned_ensembl_gene_id":"ENSG00000163825.3","gene_symbol":"RTP3","gene_name":"receptor transporter protein 3 [Source:HGNC Symbol;Acc:HGNC:15572]","synonyms":"Z3CXXC3,TMEM7,LTM1","biotype":"protein_coding","ncbi_id":"83597","summary":null,"start":46497491,"end":46500949,"strand":1,"description":"receptor transporter protein 3 [Source:HGNC Symbol;Acc:HGNC:15572]"}, {"versioned_ensembl_gene_id":"ENSG00000138669.9","gene_symbol":"PRKG2","gene_name":"protein kinase, cGMP-dependent, type II [Source:HGNC Symbol;Acc:HGNC:9416]","synonyms":"PRKGR2,cGKII","biotype":"protein_coding","ncbi_id":"5593","summary":"This gene encodes a protein that belongs to the serine/threonine protein kinase family of proteins. The encoded protein binds to and inhibits the activation of several receptor tyrosine kinases. The membrane-bound protein is a regulator of intestinal secretion, bone growth and renin secretion. Alternate splicing results in multiple transcript variants encoding distinct isoforms whose regulatory N-termini differ in length but whose C-terminal catalytic domains are identical. [provided by RefSeq, May 2018]","start":81087370,"end":81215117,"strand":-1,"description":"protein kinase, cGMP-dependent, type II [Source:HGNC Symbol;Acc:HGNC:9416]"}, {"versioned_ensembl_gene_id":"ENSG00000230511.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"NOL5BP,NOL5B,NOP56-L,dJ207F6.1","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783633,"end":28784004,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000232535.2","gene_symbol":"OR5H8","gene_name":"olfactory receptor family 5 subfamily H member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14773]","synonyms":"OR5H8P","biotype":"polymorphic_pseudogene","ncbi_id":"79289","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":98306752,"end":98312843,"strand":1,"description":"olfactory receptor family 5 subfamily H member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14773]"}, {"versioned_ensembl_gene_id":"ENSG00000225127.2","gene_symbol":"LINC00237","gene_name":"long intergenic non-protein coding RNA 237 [Source:HGNC Symbol;Acc:HGNC:38166]","synonyms":"NCRNA00237","biotype":"lincRNA","ncbi_id":"105372556","summary":null,"start":21087604,"end":21106358,"strand":-1,"description":"long intergenic non-protein coding RNA 237 [Source:HGNC Symbol;Acc:HGNC:38166]"}, {"versioned_ensembl_gene_id":"ENSG00000108515.17","gene_symbol":"ENO3","gene_name":"enolase 3 [Source:HGNC Symbol;Acc:HGNC:3354]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2027","summary":"This gene encodes one of the three enolase isoenzymes found in mammals. This isoenzyme is found in skeletal muscle cells in the adult where it may play a role in muscle development and regeneration. A switch from alpha enolase to beta enolase occurs in muscle tissue during development in rodents. Mutations in this gene have be associated glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Jul 2010]","start":4948092,"end":4957131,"strand":1,"description":"enolase 3 [Source:HGNC Symbol;Acc:HGNC:3354]"}, {"versioned_ensembl_gene_id":"ENSG00000256138.1","gene_symbol":"ZKSCAN7P1","gene_name":"zinc finger with KRAB and SCAN domains 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419827","summary":null,"start":18493051,"end":18493723,"strand":1,"description":"zinc finger with KRAB and SCAN domains 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49867]"}, {"versioned_ensembl_gene_id":"ENSG00000182263.13","gene_symbol":"FIGN","gene_name":"fidgetin, microtubule severing factor [Source:HGNC Symbol;Acc:HGNC:13285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55137","summary":null,"start":163593396,"end":163736012,"strand":-1,"description":"fidgetin, microtubule severing factor [Source:HGNC Symbol;Acc:HGNC:13285]"}, {"versioned_ensembl_gene_id":"ENSG00000106540.4","gene_symbol":"AC004837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39609717,"end":39610280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197409.7","gene_symbol":"HIST1H3D","gene_name":"histone cluster 1 H3 family member d [Source:HGNC Symbol;Acc:HGNC:4767]","synonyms":"H3/b,H3FB,H3/b,H3FB","biotype":"protein_coding","ncbi_id":"8351","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26196840,"end":26197250,"strand":-1,"description":"histone cluster 1 H3 family member d [Source:HGNC Symbol;Acc:HGNC:4767]"}, {"versioned_ensembl_gene_id":"ENSG00000274956.2","gene_symbol":"UG0898H09","gene_name":"uncharacterized LOC643763 [Source:NCBI gene;Acc:643763]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643763","summary":null,"start":62977861,"end":62984900,"strand":1,"description":"uncharacterized LOC643763 [Source:NCBI gene;Acc:643763]"}, {"versioned_ensembl_gene_id":"ENSG00000137285.9","gene_symbol":"TUBB2B","gene_name":"tubulin beta 2B class IIb [Source:HGNC Symbol;Acc:HGNC:30829]","synonyms":"MGC8685,DKFZp566F223,bA506K6.1","biotype":"protein_coding","ncbi_id":"347733","summary":"The protein encoded by this gene is a beta isoform of tubulin, which binds GTP and is a major component of microtubules. This gene is highly similar to TUBB2A and TUBB2C. Defects in this gene are a cause of asymmetric polymicrogyria. [provided by RefSeq, Mar 2010]","start":3224261,"end":3231730,"strand":-1,"description":"tubulin beta 2B class IIb [Source:HGNC Symbol;Acc:HGNC:30829]"}, {"versioned_ensembl_gene_id":"ENSG00000253517.1","gene_symbol":"XRCC6P4","gene_name":"X-ray repair cross complementing 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45186]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422546","summary":null,"start":62855068,"end":62857134,"strand":-1,"description":"X-ray repair cross complementing 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45186]"}, {"versioned_ensembl_gene_id":"ENSG00000254050.1","gene_symbol":"AC018861.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62473217,"end":62474269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277011.1","gene_symbol":"AC148477.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132282814,"end":132284606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143324.13","gene_symbol":"XPR1","gene_name":"xenotropic and polytropic retrovirus receptor 1 [Source:HGNC Symbol;Acc:HGNC:12827]","synonyms":"X3,SYG1,SLC53A1","biotype":"protein_coding","ncbi_id":"9213","summary":"The protein encoded by this gene is a receptor for the xenotropic and polytropic classes of murine leukemia viruses. The encoded protein is involved in phosphate homeostasis by mediating phosphate export from the cell. Defects in this gene have been associated with idiopathic basal ganglia calcification-6. [provided by RefSeq, Jun 2016]","start":180632004,"end":180890251,"strand":1,"description":"xenotropic and polytropic retrovirus receptor 1 [Source:HGNC Symbol;Acc:HGNC:12827]"}, {"versioned_ensembl_gene_id":"ENSG00000236076.1","gene_symbol":"LINC01072","gene_name":"long intergenic non-protein coding RNA 1072 [Source:HGNC Symbol;Acc:HGNC:49112]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355137","summary":null,"start":20102701,"end":20103230,"strand":1,"description":"long intergenic non-protein coding RNA 1072 [Source:HGNC Symbol;Acc:HGNC:49112]"}, {"versioned_ensembl_gene_id":"ENSG00000260314.2","gene_symbol":"MRC1","gene_name":"mannose receptor C-type 1 [Source:HGNC Symbol;Acc:HGNC:7228]","synonyms":"MRC1L1,CLEC13DL,CLEC13D,CD206,bA541I19.1","biotype":"protein_coding","ncbi_id":"4360","summary":"The recognition of complex carbohydrate structures on glycoproteins is an important part of several biological processes, including cell-cell recognition, serum glycoprotein turnover, and neutralization of pathogens. The protein encoded by this gene is a type I membrane receptor that mediates the endocytosis of glycoproteins by macrophages. The protein has been shown to bind high-mannose structures on the surface of potentially pathogenic viruses, bacteria, and fungi so that they can be neutralized by phagocytic engulfment.[provided by RefSeq, Sep 2015]","start":17809344,"end":17911170,"strand":1,"description":"mannose receptor C-type 1 [Source:HGNC Symbol;Acc:HGNC:7228]"}, {"versioned_ensembl_gene_id":"ENSG00000138031.14","gene_symbol":"ADCY3","gene_name":"adenylate cyclase 3 [Source:HGNC Symbol;Acc:HGNC:234]","synonyms":"AC3","biotype":"protein_coding","ncbi_id":"109","summary":"This gene encodes adenylyl cyclase 3 which is a membrane-associated enzyme and catalyzes the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). This protein appears to be widely expressed in various human tissues and may be involved in a number of physiological and pathophysiological metabolic processes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":24819169,"end":24919839,"strand":-1,"description":"adenylate cyclase 3 [Source:HGNC Symbol;Acc:HGNC:234]"}, {"versioned_ensembl_gene_id":"ENSG00000230188.1","gene_symbol":"AL158156.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37490421,"end":37490893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151623.14","gene_symbol":"NR3C2","gene_name":"nuclear receptor subfamily 3 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7979]","synonyms":"MLR,MR","biotype":"protein_coding","ncbi_id":"4306","summary":"This gene encodes the mineralocorticoid receptor, which mediates aldosterone actions on salt and water balance within restricted target cells. The protein functions as a ligand-dependent transcription factor that binds to mineralocorticoid response elements in order to transactivate target genes. Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I, a disorder characterized by urinary salt wasting. Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":148078762,"end":148444698,"strand":-1,"description":"nuclear receptor subfamily 3 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7979]"}, {"versioned_ensembl_gene_id":"ENSG00000154642.10","gene_symbol":"C21orf91","gene_name":"chromosome 21 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:16459]","synonyms":"YG81,EURL,CSSG1,C21orf38,C21orf14","biotype":"protein_coding","ncbi_id":"54149","summary":null,"start":17788967,"end":17819386,"strand":-1,"description":"chromosome 21 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:16459]"}, {"versioned_ensembl_gene_id":"ENSG00000260410.2","gene_symbol":"AC040169.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84119293,"end":84121153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267565.1","gene_symbol":"AC011477.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19892433,"end":19895847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090006.17","gene_symbol":"LTBP4","gene_name":"latent transforming growth factor beta binding protein 4 [Source:HGNC Symbol;Acc:HGNC:6717]","synonyms":"LTBP-4L,LTBP-4,FLJ90018,FLJ46318","biotype":"protein_coding","ncbi_id":"8425","summary":"The protein encoded by this gene binds transforming growth factor beta (TGFB) as it is secreted and targeted to the extracellular matrix. TGFB is biologically latent after secretion and insertion into the extracellular matrix, and sheds TGFB and other proteins upon activation. Defects in this gene may be a cause of cutis laxa and severe pulmonary, gastrointestinal, and urinary abnormalities. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":40592883,"end":40629818,"strand":1,"description":"latent transforming growth factor beta binding protein 4 [Source:HGNC Symbol;Acc:HGNC:6717]"}, {"versioned_ensembl_gene_id":"ENSG00000266667.1","gene_symbol":"AC005703.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15379864,"end":15417878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130270.16","gene_symbol":"ATP8B3","gene_name":"ATPase phospholipid transporting 8B3 [Source:HGNC Symbol;Acc:HGNC:13535]","synonyms":"ATPIK","biotype":"protein_coding","ncbi_id":"148229","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to the other. This gene encodes member 3 of phospholipid-transporting ATPase 8B; other members of this protein family are located on chromosomes 1, 15 and 18. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":1782075,"end":1812276,"strand":-1,"description":"ATPase phospholipid transporting 8B3 [Source:HGNC Symbol;Acc:HGNC:13535]"}, {"versioned_ensembl_gene_id":"ENSG00000259805.1","gene_symbol":"AC022558.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82925884,"end":83103443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220105.2","gene_symbol":"AL353151.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4781475,"end":4782078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058729.10","gene_symbol":"RIOK2","gene_name":"RIO kinase 2 [Source:HGNC Symbol;Acc:HGNC:18999]","synonyms":"FLJ11159","biotype":"protein_coding","ncbi_id":"55781","summary":null,"start":97160867,"end":97183260,"strand":-1,"description":"RIO kinase 2 [Source:HGNC Symbol;Acc:HGNC:18999]"}, {"versioned_ensembl_gene_id":"ENSG00000134001.12","gene_symbol":"EIF2S1","gene_name":"eukaryotic translation initiation factor 2 subunit alpha [Source:HGNC Symbol;Acc:HGNC:3265]","synonyms":"EIF2A,EIF2,EIF-2alpha","biotype":"protein_coding","ncbi_id":"1965","summary":"The translation initiation factor EIF2 catalyzes the first regulated step of protein synthesis initiation, promoting the binding of the initiator tRNA to 40S ribosomal subunits. Binding occurs as a ternary complex of methionyl-tRNA, EIF2, and GTP. EIF2 is composed of 3 nonidentical subunits, the 36-kD EIF2-alpha subunit (EIF2S1), the 38-kD EIF2-beta subunit (EIF2S2; MIM 603908), and the 52-kD EIF2-gamma subunit (EIF2S3; MIM 300161). The rate of formation of the ternary complex is modulated by the phosphorylation state of EIF2-alpha (Ernst et al., 1987 [PubMed 2948954]).[supplied by OMIM, Feb 2010]","start":67359997,"end":67386516,"strand":1,"description":"eukaryotic translation initiation factor 2 subunit alpha [Source:HGNC Symbol;Acc:HGNC:3265]"}, {"versioned_ensembl_gene_id":"ENSG00000224153.2","gene_symbol":"LINC02054","gene_name":"long intergenic non-protein coding RNA 2054 [Source:HGNC Symbol;Acc:HGNC:52894]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374250","summary":null,"start":184401537,"end":184439648,"strand":1,"description":"long intergenic non-protein coding RNA 2054 [Source:HGNC Symbol;Acc:HGNC:52894]"}, {"versioned_ensembl_gene_id":"ENSG00000215421.9","gene_symbol":"ZNF407","gene_name":"zinc finger protein 407 [Source:HGNC Symbol;Acc:HGNC:19904]","synonyms":"KIAA1703,FLJ20307,FLJ13839","biotype":"protein_coding","ncbi_id":"55628","summary":"This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":74597870,"end":75065671,"strand":1,"description":"zinc finger protein 407 [Source:HGNC Symbol;Acc:HGNC:19904]"}, {"versioned_ensembl_gene_id":"ENSG00000229829.1","gene_symbol":"DUTP4","gene_name":"deoxyuridine triphosphatase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39517]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873910","summary":null,"start":149817170,"end":149817644,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39517]"}, {"versioned_ensembl_gene_id":"ENSG00000264083.1","gene_symbol":"AC005899.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32430967,"end":32432841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237920.2","gene_symbol":"AL162591.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154376966,"end":154379273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233144.1","gene_symbol":"AL512656.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73381433,"end":73383496,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274677.1","gene_symbol":"AC040169.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":84085979,"end":84086590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260092.1","gene_symbol":"AC009163.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":75528532,"end":75545428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171747.8","gene_symbol":"LGALS4","gene_name":"galectin 4 [Source:HGNC Symbol;Acc:HGNC:6565]","synonyms":"GAL4","biotype":"protein_coding","ncbi_id":"3960","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. The expression of this gene is restricted to small intestine, colon, and rectum, and it is underexpressed in colorectal cancer. [provided by RefSeq, Jul 2008]","start":38801671,"end":38813364,"strand":-1,"description":"galectin 4 [Source:HGNC Symbol;Acc:HGNC:6565]"}, {"versioned_ensembl_gene_id":"ENSG00000274785.1","gene_symbol":"AC008984.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54336291,"end":54339453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234977.1","gene_symbol":"AC074389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1691906,"end":1692450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205084.10","gene_symbol":"TMEM231","gene_name":"transmembrane protein 231 [Source:HGNC Symbol;Acc:HGNC:37234]","synonyms":"PRO1886,MKS11,JBTS20,FLJ22167,ALYE870","biotype":"protein_coding","ncbi_id":"79583","summary":"This gene encodes a transmembrane protein, which is a component of the B9 complex involved in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in this gene cause Joubert syndrome (JBTS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]","start":75536744,"end":75556286,"strand":-1,"description":"transmembrane protein 231 [Source:HGNC Symbol;Acc:HGNC:37234]"}, {"versioned_ensembl_gene_id":"ENSG00000125869.9","gene_symbol":"LAMP5","gene_name":"lysosomal associated membrane protein family member 5 [Source:HGNC Symbol;Acc:HGNC:16097]","synonyms":"UNC-46,dJ1119D9.3,C20orf103,BAD-LAMP","biotype":"protein_coding","ncbi_id":"24141","summary":null,"start":9514358,"end":9530524,"strand":1,"description":"lysosomal associated membrane protein family member 5 [Source:HGNC Symbol;Acc:HGNC:16097]"}, {"versioned_ensembl_gene_id":"ENSG00000225988.1","gene_symbol":"LAMP5-AS1","gene_name":"LAMP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40754]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929329","summary":null,"start":9505180,"end":9514998,"strand":-1,"description":"LAMP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40754]"}, {"versioned_ensembl_gene_id":"ENSG00000159214.12","gene_symbol":"CCDC24","gene_name":"coiled-coil domain containing 24 [Source:HGNC Symbol;Acc:HGNC:28688]","synonyms":"MGC45441","biotype":"protein_coding","ncbi_id":"149473","summary":null,"start":43991359,"end":43996528,"strand":1,"description":"coiled-coil domain containing 24 [Source:HGNC Symbol;Acc:HGNC:28688]"}, {"versioned_ensembl_gene_id":"ENSG00000234860.1","gene_symbol":"AL162394.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99531696,"end":99536924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154415.7","gene_symbol":"PPP1R3A","gene_name":"protein phosphatase 1 regulatory subunit 3A [Source:HGNC Symbol;Acc:HGNC:9291]","synonyms":"GM,PPP1R3","biotype":"protein_coding","ncbi_id":"5506","summary":"The glycogen-associated form of protein phosphatase-1 (PP1) derived from skeletal muscle is a heterodimer composed of a 37-kD catalytic subunit and a 124-kD targeting and regulatory subunit. This gene encodes the regulatory subunit which binds to muscle glycogen with high affinity, thereby enhancing dephosphorylation of glycogen-bound substrates for PP1 such as glycogen synthase and glycogen phosphorylase kinase. [provided by RefSeq, Jul 2008]","start":113876777,"end":114075920,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 3A [Source:HGNC Symbol;Acc:HGNC:9291]"}, {"versioned_ensembl_gene_id":"ENSG00000105875.13","gene_symbol":"WDR91","gene_name":"WD repeat domain 91 [Source:HGNC Symbol;Acc:HGNC:24997]","synonyms":"SORF-1,HSPC049","biotype":"protein_coding","ncbi_id":"29062","summary":null,"start":135183839,"end":135211534,"strand":-1,"description":"WD repeat domain 91 [Source:HGNC Symbol;Acc:HGNC:24997]"}, {"versioned_ensembl_gene_id":"ENSG00000147789.15","gene_symbol":"ZNF7","gene_name":"zinc finger protein 7 [Source:HGNC Symbol;Acc:HGNC:13139]","synonyms":"KOX4,HF.16","biotype":"protein_coding","ncbi_id":"7553","summary":null,"start":144827464,"end":144847509,"strand":1,"description":"zinc finger protein 7 [Source:HGNC Symbol;Acc:HGNC:13139]"}, {"versioned_ensembl_gene_id":"ENSG00000266498.1","gene_symbol":"AC055811.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17235433,"end":17236118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225442.2","gene_symbol":"MPRIP-AS1","gene_name":"MPRIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41263]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874529","summary":null,"start":17076038,"end":17077752,"strand":-1,"description":"MPRIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41263]"}, {"versioned_ensembl_gene_id":"ENSG00000254688.1","gene_symbol":"AC013549.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12822435,"end":12823667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107290.13","gene_symbol":"SETX","gene_name":"senataxin [Source:HGNC Symbol;Acc:HGNC:445]","synonyms":"Sen1,SCAR1,KIAA0625,AOA2,ALS4","biotype":"protein_coding","ncbi_id":"23064","summary":"This gene encodes a protein named for its homology to the Sen1p protein of fungi which has RNA helicase activity encoded by a domain at the C-terminal end of the protein. The protein encoded by this gene contains a DNA/RNA helicase domain at its C-terminal end which suggests that it may be involved in both DNA and RNA processing. Mutations in this gene have been associated with ataxia-ocular apraxia-2 (AOA2) and an autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS4). [provided by RefSeq, Jul 2008]","start":132261356,"end":132354985,"strand":-1,"description":"senataxin [Source:HGNC Symbol;Acc:HGNC:445]"}, {"versioned_ensembl_gene_id":"ENSG00000250611.1","gene_symbol":"AC098862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20037560,"end":20037972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238238.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31568197,"end":31569712,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000279918.1","gene_symbol":"AC006840.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19098199,"end":19098740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258668.1","gene_symbol":"COX6CP11","gene_name":"cytochrome c oxidase subunit 6C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480266","summary":null,"start":77652827,"end":77653055,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49363]"}, {"versioned_ensembl_gene_id":"ENSG00000116906.11","gene_symbol":"GNPAT","gene_name":"glyceronephosphate O-acyltransferase [Source:HGNC Symbol;Acc:HGNC:4416]","synonyms":"DHAPAT,DAPAT,DAP-AT","biotype":"protein_coding","ncbi_id":"8443","summary":"This gene encodes an enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in this gene are associated with rhizomelic chondrodysplasia punctata. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":231241207,"end":231277973,"strand":1,"description":"glyceronephosphate O-acyltransferase [Source:HGNC Symbol;Acc:HGNC:4416]"}, {"versioned_ensembl_gene_id":"ENSG00000109472.13","gene_symbol":"CPE","gene_name":"carboxypeptidase E [Source:HGNC Symbol;Acc:HGNC:2303]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1363","summary":"This gene encodes a member of the M14 family of metallocarboxypeptidases. The encoded preproprotein is proteolytically processed to generate the mature peptidase. This peripheral membrane protein cleaves C-terminal amino acid residues and is involved in the biosynthesis of peptide hormones and neurotransmitters, including insulin. This protein may also function independently of its peptidase activity, as a neurotrophic factor that promotes neuronal survival, and as a sorting receptor that binds to regulated secretory pathway proteins, including prohormones. Mutations in this gene are implicated in type 2 diabetes. [provided by RefSeq, Nov 2015]","start":165361194,"end":165498320,"strand":1,"description":"carboxypeptidase E [Source:HGNC Symbol;Acc:HGNC:2303]"}, {"versioned_ensembl_gene_id":"ENSG00000282351.1","gene_symbol":"MAPK8IP1P2","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52402]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644172","summary":null,"start":45612507,"end":45613978,"strand":-1,"description":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52402]"}, {"versioned_ensembl_gene_id":"ENSG00000100593.17","gene_symbol":"ISM2","gene_name":"isthmin 2 [Source:HGNC Symbol;Acc:HGNC:23176]","synonyms":"THSD3,TAIL1,FLJ32147","biotype":"protein_coding","ncbi_id":"145501","summary":"The protein encoded by this gene contains a type 1 thrombospondin domain, which is present in thrombospondin, a number of proteins involved in the complement pathway, as well as in extracellular matrix proteins. Two alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Mar 2009]","start":77474394,"end":77498850,"strand":-1,"description":"isthmin 2 [Source:HGNC Symbol;Acc:HGNC:23176]"}, {"versioned_ensembl_gene_id":"ENSG00000228177.2","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"D6S53E,G4","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31697751,"end":31700226,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000277399.4","gene_symbol":"GPR179","gene_name":"G protein-coupled receptor 179 [Source:HGNC Symbol;Acc:HGNC:31371]","synonyms":"GPR158L1,CSNB1E","biotype":"protein_coding","ncbi_id":"440435","summary":"This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]","start":38325530,"end":38343847,"strand":-1,"description":"G protein-coupled receptor 179 [Source:HGNC Symbol;Acc:HGNC:31371]"}, {"versioned_ensembl_gene_id":"ENSG00000230686.1","gene_symbol":"AC067945.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":191017954,"end":191019079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129518.8","gene_symbol":"EAPP","gene_name":"E2F associated phosphoprotein [Source:HGNC Symbol;Acc:HGNC:19312]","synonyms":"FLJ20578,C14orf11,BM036","biotype":"protein_coding","ncbi_id":"55837","summary":"This gene encodes a phosphoprotein that interacts with several members of the E2F family of proteins. The protein localizes to the nucleus, and is present throughout the cell cycle except during mitosis. It functions to modulate E2F-regulated transcription and stimulate proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":34515929,"end":34539711,"strand":-1,"description":"E2F associated phosphoprotein [Source:HGNC Symbol;Acc:HGNC:19312]"}, {"versioned_ensembl_gene_id":"ENSG00000205266.9","gene_symbol":"KRT17P5","gene_name":"keratin 17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50723]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339240","summary":null,"start":18415728,"end":18425097,"strand":1,"description":"keratin 17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50723]"}, {"versioned_ensembl_gene_id":"ENSG00000189182.9","gene_symbol":"KRT77","gene_name":"keratin 77 [Source:HGNC Symbol;Acc:HGNC:20411]","synonyms":"KRT1B","biotype":"protein_coding","ncbi_id":"374454","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes an epithelial keratin that is expressed in the skin and eccrine sweat glands. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]","start":52689626,"end":52703463,"strand":-1,"description":"keratin 77 [Source:HGNC Symbol;Acc:HGNC:20411]"}, {"versioned_ensembl_gene_id":"ENSG00000253397.1","gene_symbol":"AC069113.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27904481,"end":27910310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166246.13","gene_symbol":"C16orf71","gene_name":"chromosome 16 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:25081]","synonyms":"FLJ43261,DKFZp686H2240","biotype":"protein_coding","ncbi_id":"146562","summary":null,"start":4734272,"end":4749396,"strand":1,"description":"chromosome 16 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:25081]"}, {"versioned_ensembl_gene_id":"ENSG00000246541.2","gene_symbol":"AC096746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94117792,"end":94207556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198799.11","gene_symbol":"LRIG2","gene_name":"leucine rich repeats and immunoglobulin like domains 2 [Source:HGNC Symbol;Acc:HGNC:20889]","synonyms":"KIAA0806","biotype":"protein_coding","ncbi_id":"9860","summary":"This gene encodes a transmembrane protein containing leucine-rich repeats and immunoglobulin-like domains. The encoded protein promotes epidermal growth factor signalling, resulting in increased proliferation. Its expression in the cytoplasm of glioma cells is correlated with poor survival. Mutations in this gene can cause urofacial syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":113073209,"end":113132260,"strand":1,"description":"leucine rich repeats and immunoglobulin like domains 2 [Source:HGNC Symbol;Acc:HGNC:20889]"}, {"versioned_ensembl_gene_id":"ENSG00000282331.1","gene_symbol":"LRRC37A4P","gene_name":"leucine rich repeat containing 37 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:25479]","synonyms":"LRRC37A4,FLJ10120","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"55073","summary":null,"start":45506393,"end":45561970,"strand":-1,"description":"leucine rich repeat containing 37 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:25479]"}, {"versioned_ensembl_gene_id":"ENSG00000253927.1","gene_symbol":"AC002428.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135900353,"end":135918161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231018.1","gene_symbol":"EIF4A1P3","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462824","summary":null,"start":131782570,"end":131782813,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37922]"}, {"versioned_ensembl_gene_id":"ENSG00000172238.4","gene_symbol":"ATOH1","gene_name":"atonal bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:797]","synonyms":"bHLHa14,Math1,MATH-1,HATH1","biotype":"protein_coding","ncbi_id":"474","summary":"This protein belongs to the basic helix-loop-helix (BHLH) family of transcription factors. It activates E-box dependent transcription along with E47. [provided by RefSeq, Jul 2008]","start":93828753,"end":93830964,"strand":1,"description":"atonal bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:797]"}, {"versioned_ensembl_gene_id":"ENSG00000249140.1","gene_symbol":"PRDX2P3","gene_name":"peroxiredoxin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418943","summary":null,"start":179572156,"end":179572741,"strand":1,"description":"peroxiredoxin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44968]"}, {"versioned_ensembl_gene_id":"ENSG00000106799.12","gene_symbol":"TGFBR1","gene_name":"transforming growth factor beta receptor 1 [Source:HGNC Symbol;Acc:HGNC:11772]","synonyms":"ACVRLK4,MSSE,ESS1,ALK5,ALK-5","biotype":"protein_coding","ncbi_id":"7046","summary":"The protein encoded by this gene forms a heteromeric complex with type II TGF-beta receptors when bound to TGF-beta, transducing the TGF-beta signal from the cell surface to the cytoplasm. The encoded protein is a serine/threonine protein kinase. Mutations in this gene have been associated with Loeys-Dietz aortic aneurysm syndrome (LDAS). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":99104038,"end":99154192,"strand":1,"description":"transforming growth factor beta receptor 1 [Source:HGNC Symbol;Acc:HGNC:11772]"}, {"versioned_ensembl_gene_id":"ENSG00000258073.1","gene_symbol":"AC128657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84939524,"end":84939668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144559.10","gene_symbol":"TAMM41","gene_name":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]","synonyms":"MGC16471,DKFZp434E0519,C3orf31","biotype":"protein_coding","ncbi_id":"132001","summary":null,"start":11790442,"end":11846919,"strand":-1,"description":"TAM41 mitochondrial translocator assembly and maintenance homolog [Source:HGNC Symbol;Acc:HGNC:25187]"}, {"versioned_ensembl_gene_id":"ENSG00000241127.7","gene_symbol":"YAE1D1","gene_name":"Yae1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24857]","synonyms":"GK003,C7orf36","biotype":"protein_coding","ncbi_id":"57002","summary":null,"start":39566376,"end":39610320,"strand":1,"description":"Yae1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24857]"}, {"versioned_ensembl_gene_id":"ENSG00000176973.7","gene_symbol":"FAM89B","gene_name":"family with sequence similarity 89 member B [Source:HGNC Symbol;Acc:HGNC:16708]","synonyms":"MTVR1,LRAP25","biotype":"protein_coding","ncbi_id":"23625","summary":null,"start":65572349,"end":65574198,"strand":1,"description":"family with sequence similarity 89 member B [Source:HGNC Symbol;Acc:HGNC:16708]"}, {"versioned_ensembl_gene_id":"ENSG00000148218.15","gene_symbol":"ALAD","gene_name":"aminolevulinate dehydratase [Source:HGNC Symbol;Acc:HGNC:395]","synonyms":"PBGS,ALADH","biotype":"protein_coding","ncbi_id":"210","summary":"The ALAD enzyme is composed of 8 identical subunits and catalyzes the condensation of 2 molecules of delta-aminolevulinate to form porphobilinogen (a precursor of heme, cytochromes and other hemoproteins). ALAD catalyzes the second step in the porphyrin and heme biosynthetic pathway; zinc is essential for enzymatic activity. ALAD enzymatic activity is inhibited by lead and a defect in the ALAD structural gene can cause increased sensitivity to lead poisoning and acute hepatic porphyria. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":113386317,"end":113401333,"strand":-1,"description":"aminolevulinate dehydratase [Source:HGNC Symbol;Acc:HGNC:395]"}, {"versioned_ensembl_gene_id":"ENSG00000226780.1","gene_symbol":"AC244035.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206117783,"end":206126805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223372.7","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33145868,"end":33150636,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000267207.1","gene_symbol":"AC005884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61034636,"end":61070122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156411.9","gene_symbol":"C14orf2","gene_name":"chromosome 14 open reading frame 2 [Source:HGNC Symbol;Acc:HGNC:1188]","synonyms":"MLQ,6.8PL,MP68","biotype":"protein_coding","ncbi_id":"9556","summary":null,"start":103912288,"end":103928269,"strand":-1,"description":"chromosome 14 open reading frame 2 [Source:HGNC Symbol;Acc:HGNC:1188]"}, {"versioned_ensembl_gene_id":"ENSG00000249503.1","gene_symbol":"HMGN1P16","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874442","summary":null,"start":148221360,"end":148221642,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39360]"}, {"versioned_ensembl_gene_id":"ENSG00000154274.14","gene_symbol":"C4orf19","gene_name":"chromosome 4 open reading frame 19 [Source:HGNC Symbol;Acc:HGNC:25618]","synonyms":"FLJ11017","biotype":"protein_coding","ncbi_id":"55286","summary":null,"start":37453941,"end":37623495,"strand":1,"description":"chromosome 4 open reading frame 19 [Source:HGNC Symbol;Acc:HGNC:25618]"}, {"versioned_ensembl_gene_id":"ENSG00000259734.1","gene_symbol":"AC012229.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86630266,"end":86631136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266958.1","gene_symbol":"AC005779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45187388,"end":45216933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113361.12","gene_symbol":"CDH6","gene_name":"cadherin 6 [Source:HGNC Symbol;Acc:HGNC:1765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1004","summary":"This gene encodes a member of the cadherin superfamily. Cadherins are membrane glycoproteins that mediate homophilic cell-cell adhesion and play critical roles in cell differentiation and morphogenesis. The encoded protein is a type II cadherin and may play a role in kidney development as well as endometrium and placenta formation. Decreased expression of this gene may be associated with tumor growth and metastasis. [provided by RefSeq, May 2011]","start":31193750,"end":31329146,"strand":1,"description":"cadherin 6 [Source:HGNC Symbol;Acc:HGNC:1765]"}, {"versioned_ensembl_gene_id":"ENSG00000224254.2","gene_symbol":"MTCO1P39","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52104]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075282","summary":null,"start":19605454,"end":19605933,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52104]"}, {"versioned_ensembl_gene_id":"ENSG00000145824.12","gene_symbol":"CXCL14","gene_name":"C-X-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10640]","synonyms":"KS1,Kec,BRAK,bolekine,BMAC,SCYB14,NJAC,MIP-2g","biotype":"protein_coding","ncbi_id":"9547","summary":"This antimicrobial gene belongs to the cytokine gene family which encode secreted proteins involved in immunoregulatory and inflammatory processes. The protein encoded by this gene is structurally related to the CXC (Cys-X-Cys) subfamily of cytokines. Members of this subfamily are characterized by two cysteines separated by a single amino acid. This cytokine displays chemotactic activity for monocytes but not for lymphocytes, dendritic cells, neutrophils or macrophages. It has been implicated that this cytokine is involved in the homeostasis of monocyte-derived macrophages rather than in inflammation. [provided by RefSeq, Sep 2014]","start":135570679,"end":135579279,"strand":-1,"description":"C-X-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10640]"}, {"versioned_ensembl_gene_id":"ENSG00000253109.1","gene_symbol":"RPL12P22","gene_name":"ribosomal protein L12 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270922","summary":null,"start":174039751,"end":174040240,"strand":-1,"description":"ribosomal protein L12 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35762]"}, {"versioned_ensembl_gene_id":"ENSG00000237991.3","gene_symbol":"RPL35P1","gene_name":"ribosomal protein L35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440737","summary":null,"start":236981339,"end":236981708,"strand":1,"description":"ribosomal protein L35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36695]"}, {"versioned_ensembl_gene_id":"ENSG00000255222.1","gene_symbol":"SETP17","gene_name":"SET pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130043","summary":null,"start":86294760,"end":86295576,"strand":1,"description":"SET pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42936]"}, {"versioned_ensembl_gene_id":"ENSG00000186063.12","gene_symbol":"AIDA","gene_name":"axin interactor, dorsalization associated [Source:HGNC Symbol;Acc:HGNC:25761]","synonyms":"FLJ12806,C1orf80","biotype":"protein_coding","ncbi_id":"64853","summary":null,"start":222668013,"end":222713210,"strand":-1,"description":"axin interactor, dorsalization associated [Source:HGNC Symbol;Acc:HGNC:25761]"}, {"versioned_ensembl_gene_id":"ENSG00000090534.17","gene_symbol":"THPO","gene_name":"thrombopoietin [Source:HGNC Symbol;Acc:HGNC:11795]","synonyms":"MPLLG,MGDF,TPO","biotype":"protein_coding","ncbi_id":"7066","summary":"Megakaryocytopoiesis is the cellular development process that leads to platelet production. The main functional protein encoded by this gene is a humoral growth factor that is necessary for megakaryocyte proliferation and maturation, as well as for thrombopoiesis. This protein is the ligand for MLP/C_MPL, the product of myeloproliferative leukemia virus oncogene. Mutations in this gene are the cause of thrombocythemia 1. Alternative promoter usage and differential splicing result in multiple transcript variants differing in the 5' UTR and/or coding region. Multiple AUG codons upstream of the main open reading frame (ORF) have been identified, and these upstream AUGs inhibit translation of the main ORF at different extent. [provided by RefSeq, Feb 2014]","start":184371935,"end":184378144,"strand":-1,"description":"thrombopoietin [Source:HGNC Symbol;Acc:HGNC:11795]"}, {"versioned_ensembl_gene_id":"ENSG00000256098.1","gene_symbol":"AP002392.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74142151,"end":74142358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215866.7","gene_symbol":"LINC01356","gene_name":"long intergenic non-protein coding RNA 1356 [Source:HGNC Symbol;Acc:HGNC:50587]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996702","summary":null,"start":112820170,"end":112850643,"strand":-1,"description":"long intergenic non-protein coding RNA 1356 [Source:HGNC Symbol;Acc:HGNC:50587]"}, {"versioned_ensembl_gene_id":"ENSG00000246211.2","gene_symbol":"P4HA3-AS1","gene_name":"P4HA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53160]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928580","summary":null,"start":74311362,"end":74324705,"strand":1,"description":"P4HA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53160]"}, {"versioned_ensembl_gene_id":"ENSG00000249639.1","gene_symbol":"AC022092.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135450613,"end":135458697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138449.10","gene_symbol":"SLC40A1","gene_name":"solute carrier family 40 member 1 [Source:HGNC Symbol;Acc:HGNC:10909]","synonyms":"MTP1,IREG1,HFE4,FPN1,SLC11A3","biotype":"protein_coding","ncbi_id":"30061","summary":"The protein encoded by this gene is a cell membrane protein that may be involved in iron export from duodenal epithelial cells. Defects in this gene are a cause of hemochromatosis type 4 (HFE4). [provided by RefSeq, Jul 2008]","start":189560579,"end":189583758,"strand":-1,"description":"solute carrier family 40 member 1 [Source:HGNC Symbol;Acc:HGNC:10909]"}, {"versioned_ensembl_gene_id":"ENSG00000259416.2","gene_symbol":"AC021739.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85754941,"end":85756237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268912.1","gene_symbol":"AC012313.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58428632,"end":58431148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259762.1","gene_symbol":"AC021739.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85750336,"end":85752901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226554.1","gene_symbol":"MTCL1P1","gene_name":"MTCL1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42040]","synonyms":"SOGA2P1,CCDC165P1","biotype":"processed_pseudogene","ncbi_id":"100288130","summary":null,"start":70923664,"end":70924455,"strand":1,"description":"MTCL1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42040]"}, {"versioned_ensembl_gene_id":"ENSG00000104499.6","gene_symbol":"GML","gene_name":"glycosylphosphatidylinositol anchored molecule like [Source:HGNC Symbol;Acc:HGNC:4375]","synonyms":"LY6DL","biotype":"protein_coding","ncbi_id":"2765","summary":null,"start":142834247,"end":142916506,"strand":1,"description":"glycosylphosphatidylinositol anchored molecule like [Source:HGNC Symbol;Acc:HGNC:4375]"}, {"versioned_ensembl_gene_id":"ENSG00000277961.1","gene_symbol":"AC010518.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54294649,"end":54294966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231327.1","gene_symbol":"LINC01816","gene_name":"long intergenic non-protein coding RNA 1816 [Source:HGNC Symbol;Acc:HGNC:52621]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133985","summary":null,"start":70124036,"end":70125317,"strand":-1,"description":"long intergenic non-protein coding RNA 1816 [Source:HGNC Symbol;Acc:HGNC:52621]"}, {"versioned_ensembl_gene_id":"ENSG00000232492.1","gene_symbol":"NPM1P13","gene_name":"nucleophosmin 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:7915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10834","summary":null,"start":18948898,"end":18949762,"strand":-1,"description":"nucleophosmin 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:7915]"}, {"versioned_ensembl_gene_id":"ENSG00000180104.15","gene_symbol":"EXOC3","gene_name":"exocyst complex component 3 [Source:HGNC Symbol;Acc:HGNC:30378]","synonyms":"Sec6p,SEC6L1","biotype":"protein_coding","ncbi_id":"11336","summary":"The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. [provided by RefSeq, Jul 2008]","start":443158,"end":471937,"strand":1,"description":"exocyst complex component 3 [Source:HGNC Symbol;Acc:HGNC:30378]"}, {"versioned_ensembl_gene_id":"ENSG00000232493.2","gene_symbol":"RPL12P11","gene_name":"ribosomal protein L12 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:15835]","synonyms":"RPL12L2,dJ661I20.1","biotype":"processed_pseudogene","ncbi_id":"128467","summary":null,"start":41547422,"end":41547922,"strand":1,"description":"ribosomal protein L12 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:15835]"}, {"versioned_ensembl_gene_id":"ENSG00000169105.7","gene_symbol":"CHST14","gene_name":"carbohydrate sulfotransferase 14 [Source:HGNC Symbol;Acc:HGNC:24464]","synonyms":"D4ST1,D4ST-1,HD4ST","biotype":"protein_coding","ncbi_id":"113189","summary":"This gene encodes a member of the HNK-1 family of sulfotransferases. The encoded protein transfers sulfate to the C-4 hydroxyl of N-acetylgalactosamine residues in dermatan sulfate. Mutations in this gene have been associated with adducted thumb-clubfoot syndrome.[provided by RefSeq, Mar 2010]","start":40470998,"end":40474571,"strand":1,"description":"carbohydrate sulfotransferase 14 [Source:HGNC Symbol;Acc:HGNC:24464]"}, {"versioned_ensembl_gene_id":"ENSG00000233584.9","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33266563,"end":33282911,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000226591.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33257906,"end":33261442,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000072041.16","gene_symbol":"SLC6A15","gene_name":"solute carrier family 6 member 15 [Source:HGNC Symbol;Acc:HGNC:13621]","synonyms":"V7-3,SBAT1,NTT73,hv7-3,FLJ10316","biotype":"protein_coding","ncbi_id":"55117","summary":"This gene encodes a member of the solute carrier family 6 protein family which transports neutral amino acids. The encoded protein is thought to play a role in neuronal amino acid transport (PMID: 16185194) and may be associated with major depression (PMID: 21521612). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":84859488,"end":84913615,"strand":-1,"description":"solute carrier family 6 member 15 [Source:HGNC Symbol;Acc:HGNC:13621]"}, {"versioned_ensembl_gene_id":"ENSG00000153048.10","gene_symbol":"CARHSP1","gene_name":"calcium regulated heat stable protein 1 [Source:HGNC Symbol;Acc:HGNC:17150]","synonyms":"CSDC1,CRHSP-24","biotype":"protein_coding","ncbi_id":"23589","summary":null,"start":8852942,"end":8869012,"strand":-1,"description":"calcium regulated heat stable protein 1 [Source:HGNC Symbol;Acc:HGNC:17150]"}, {"versioned_ensembl_gene_id":"ENSG00000259939.1","gene_symbol":"AC022167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8853312,"end":8854347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259364.1","gene_symbol":"AC013356.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40453444,"end":40454639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267772.1","gene_symbol":"LINC01999","gene_name":"long intergenic non-protein coding RNA 1999 [Source:HGNC Symbol;Acc:HGNC:52834]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388406","summary":null,"start":60564547,"end":60586623,"strand":1,"description":"long intergenic non-protein coding RNA 1999 [Source:HGNC Symbol;Acc:HGNC:52834]"}, {"versioned_ensembl_gene_id":"ENSG00000137745.11","gene_symbol":"MMP13","gene_name":"matrix metallopeptidase 13 [Source:HGNC Symbol;Acc:HGNC:7159]","synonyms":"CLG3","biotype":"protein_coding","ncbi_id":"4322","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This protease cleaves type II collagen more efficiently than types I and III. It may be involved in articular cartilage turnover and cartilage pathophysiology associated with osteoarthritis. Mutations in this gene are associated with metaphyseal anadysplasia. This gene is part of a cluster of MMP genes on chromosome 11. [provided by RefSeq, Jan 2016]","start":102942995,"end":102955734,"strand":-1,"description":"matrix metallopeptidase 13 [Source:HGNC Symbol;Acc:HGNC:7159]"}, {"versioned_ensembl_gene_id":"ENSG00000021488.12","gene_symbol":"SLC7A9","gene_name":"solute carrier family 7 member 9 [Source:HGNC Symbol;Acc:HGNC:11067]","synonyms":"CSNU3","biotype":"protein_coding","ncbi_id":"11136","summary":"This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011]","start":32830509,"end":32869766,"strand":-1,"description":"solute carrier family 7 member 9 [Source:HGNC Symbol;Acc:HGNC:11067]"}, {"versioned_ensembl_gene_id":"ENSG00000267222.1","gene_symbol":"AC107993.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42495867,"end":42496550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267632.1","gene_symbol":"AC067852.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42509784,"end":42511519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233109.4","gene_symbol":"AC013701.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48913916,"end":48914380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233523.1","gene_symbol":"PHBP5","gene_name":"prohibitin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39284]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478939","summary":null,"start":73187969,"end":73188736,"strand":-1,"description":"prohibitin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39284]"}, {"versioned_ensembl_gene_id":"ENSG00000233996.1","gene_symbol":"AC013439.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189486480,"end":189487992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104859.14","gene_symbol":"CLASRP","gene_name":"CLK4 associating serine/arginine rich protein [Source:HGNC Symbol;Acc:HGNC:17731]","synonyms":"SWAP2,SFRS16,CLASP","biotype":"protein_coding","ncbi_id":"11129","summary":null,"start":45039040,"end":45070956,"strand":1,"description":"CLK4 associating serine/arginine rich protein [Source:HGNC Symbol;Acc:HGNC:17731]"}, {"versioned_ensembl_gene_id":"ENSG00000229156.1","gene_symbol":"CR769776.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64462819,"end":64463196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235176.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"RPA12,HTEX-6,tctex-6,hZR14","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30054063,"end":30060065,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000254873.1","gene_symbol":"AP001267.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118397095,"end":118401895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230915.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29951762,"end":29953727,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000223439.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"CDA12,HLA-59,D6S203,HLA-CDA12","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":30001721,"end":30005094,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000255244.1","gene_symbol":"AC023078.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18934985,"end":18939721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220412.1","gene_symbol":"AL356234.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137705423,"end":137707201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250644.3","gene_symbol":"AC068580.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1734821,"end":1763954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253702.1","gene_symbol":"AC026904.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48597458,"end":48621018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282360.1","gene_symbol":"ELK2AP","gene_name":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]","synonyms":"ELK2P1,ELK2.1,ELK2","biotype":"processed_pseudogene","ncbi_id":"2003","summary":null,"start":105673079,"end":105674085,"strand":-1,"description":"ELK2A, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3323]"}, {"versioned_ensembl_gene_id":"ENSG00000088808.16","gene_symbol":"PPP1R13B","gene_name":"protein phosphatase 1 regulatory subunit 13B [Source:HGNC Symbol;Acc:HGNC:14950]","synonyms":"p53BP2-like,KIAA0771,ASPP1,p85","biotype":"protein_coding","ncbi_id":"23368","summary":"This gene encodes a member of the ASPP (apoptosis-stimulating protein of p53) family of p53 interacting proteins. The protein contains four ankyrin repeats and an SH3 domain involved in protein-protein interactions. ASPP proteins are required for the induction of apoptosis by p53-family proteins. They promote DNA binding and transactivation of p53-family proteins on the promoters of proapoptotic genes. Expression of this gene is regulated by the E2F transcription factor. [provided by RefSeq, Jul 2008]","start":103733752,"end":103847590,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 13B [Source:HGNC Symbol;Acc:HGNC:14950]"}, {"versioned_ensembl_gene_id":"ENSG00000253455.1","gene_symbol":"AC022915.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48620465,"end":48623895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255355.1","gene_symbol":"AP000640.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":59669312,"end":59676041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087365.15","gene_symbol":"SF3B2","gene_name":"splicing factor 3b subunit 2 [Source:HGNC Symbol;Acc:HGNC:10769]","synonyms":"SF3b1,SAP145,Cus1,SF3b145","biotype":"protein_coding","ncbi_id":"10992","summary":"This gene encodes subunit 2 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence-independent manner and may anchor the U2 snRNP to the pre-mRNA. Splicing factor 3b is also a component of the minor U12-type spliceosome. Subunit 2 associates with pre-mRNA upstream of the branch site at the anchoring site. Subunit 2 also interacts directly with subunit 4 of the splicing factor 3b complex. Subunit 2 is a highly hydrophilic protein with a proline-rich N-terminus and a glutamate-rich stretch in the C-terminus. [provided by RefSeq, Jul 2008]","start":66050729,"end":66069308,"strand":1,"description":"splicing factor 3b subunit 2 [Source:HGNC Symbol;Acc:HGNC:10769]"}, {"versioned_ensembl_gene_id":"ENSG00000270068.1","gene_symbol":"AC125494.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6723233,"end":6723687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174021.10","gene_symbol":"GNG5","gene_name":"G protein subunit gamma 5 [Source:HGNC Symbol;Acc:HGNC:4408]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2787","summary":"G proteins are trimeric (alpha-beta-gamma) membrane-associated proteins that regulate flow of information from cell surface receptors to a variety of internal metabolic effectors. Interaction of a G protein with its activated receptor promotes exchange of GTP for GDP that is bound to the alpha subunit. The alpha-GTP complex dissociates from the beta-gamma heterodimer so that the subunits, in turn, may interact with and regulate effector molecules (Gilman, 1987 [PubMed 3113327]; summary by Ahmad et al., 1995) [PubMed 7606925].[supplied by OMIM, Nov 2010]","start":84498325,"end":84506565,"strand":-1,"description":"G protein subunit gamma 5 [Source:HGNC Symbol;Acc:HGNC:4408]"}, {"versioned_ensembl_gene_id":"ENSG00000255314.2","gene_symbol":"AC024475.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46123573,"end":46177106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122085.16","gene_symbol":"MTERF4","gene_name":"mitochondrial transcription termination factor 4 [Source:HGNC Symbol;Acc:HGNC:28785]","synonyms":"MTERFD2,MGC61716","biotype":"protein_coding","ncbi_id":"130916","summary":null,"start":241072169,"end":241102332,"strand":-1,"description":"mitochondrial transcription termination factor 4 [Source:HGNC Symbol;Acc:HGNC:28785]"}, {"versioned_ensembl_gene_id":"ENSG00000261024.7","gene_symbol":"GS1-279B7.1","gene_name":"microtubule associated protein 1 light chain 3 beta pseudogene [Source:NCBI gene;Acc:100288079]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100288079","summary":null,"start":185321157,"end":185335039,"strand":-1,"description":"microtubule associated protein 1 light chain 3 beta pseudogene [Source:NCBI gene;Acc:100288079]"}, {"versioned_ensembl_gene_id":"ENSG00000118156.12","gene_symbol":"ZNF541","gene_name":"zinc finger protein 541 [Source:HGNC Symbol;Acc:HGNC:25294]","synonyms":"DKFZp434I1930","biotype":"protein_coding","ncbi_id":"84215","summary":null,"start":47520685,"end":47555856,"strand":-1,"description":"zinc finger protein 541 [Source:HGNC Symbol;Acc:HGNC:25294]"}, {"versioned_ensembl_gene_id":"ENSG00000227038.3","gene_symbol":"GTF2IP7","gene_name":"general transcription factor IIi pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51720]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101927126","summary":null,"start":76090431,"end":76108779,"strand":-1,"description":"general transcription factor IIi pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51720]"}, {"versioned_ensembl_gene_id":"ENSG00000233893.1","gene_symbol":"EZR-AS1","gene_name":"EZR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40609]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101409257","summary":null,"start":158818011,"end":158820593,"strand":1,"description":"EZR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40609]"}, {"versioned_ensembl_gene_id":"ENSG00000230882.1","gene_symbol":"AC005077.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76071469,"end":76074963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164169.12","gene_symbol":"PRMT9","gene_name":"protein arginine methyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:25099]","synonyms":"PRMT10,FLJ46629","biotype":"protein_coding","ncbi_id":"90826","summary":"This gene encodes a type II methyltransferase. Post-translational modification of target proteins by PRMTs plays an important regulatory role in many biological processes, whereby PRMTs methylate arginine residues by transferring methyl groups from S-adenosyl-L-methionine to the guanidino nitrogen atoms of arginine. The protein encoded by this gene methylates spliceosome associated protein 145 to regulate alternative splicing and acts as a modulator of small nuclear ribonucleoprotein maturation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2017]","start":147637785,"end":147684230,"strand":-1,"description":"protein arginine methyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:25099]"}, {"versioned_ensembl_gene_id":"ENSG00000132196.13","gene_symbol":"HSD17B7","gene_name":"hydroxysteroid 17-beta dehydrogenase 7 [Source:HGNC Symbol;Acc:HGNC:5215]","synonyms":"SDR37C1,PRAP","biotype":"protein_coding","ncbi_id":"51478","summary":"HSD17B7 encodes an enzyme that functions both as a 17-beta-hydroxysteroid dehydrogenase (EC 1.1.1.62) in the biosynthesis of sex steroids and as a 3-ketosteroid reductase (EC 1.1.1.270) in the biosynthesis of cholesterol (Marijanovic et al., 2003 [PubMed 12829805]).[supplied by OMIM, May 2010]","start":162790702,"end":162812817,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 7 [Source:HGNC Symbol;Acc:HGNC:5215]"}, {"versioned_ensembl_gene_id":"ENSG00000280073.1","gene_symbol":"AL157996.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69357010,"end":69359308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213965.3","gene_symbol":"NUDT19","gene_name":"nudix hydrolase 19 [Source:HGNC Symbol;Acc:HGNC:32036]","synonyms":"RP2","biotype":"protein_coding","ncbi_id":"390916","summary":null,"start":32691961,"end":32713796,"strand":1,"description":"nudix hydrolase 19 [Source:HGNC Symbol;Acc:HGNC:32036]"}, {"versioned_ensembl_gene_id":"ENSG00000251593.1","gene_symbol":"MSNP1","gene_name":"moesin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7374]","synonyms":"MSNL1","biotype":"processed_pseudogene","ncbi_id":"4479","summary":null,"start":25909503,"end":25911234,"strand":1,"description":"moesin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7374]"}, {"versioned_ensembl_gene_id":"ENSG00000279869.1","gene_symbol":"AC022418.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25716271,"end":25716715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264895.1","gene_symbol":"AC006141.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51249579,"end":51251748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061987.15","gene_symbol":"MON2","gene_name":"MON2 homolog, regulator of endosome-to-Golgi trafficking [Source:HGNC Symbol;Acc:HGNC:29177]","synonyms":"KIAA1040","biotype":"protein_coding","ncbi_id":"23041","summary":null,"start":62466817,"end":62600479,"strand":1,"description":"MON2 homolog, regulator of endosome-to-Golgi trafficking [Source:HGNC Symbol;Acc:HGNC:29177]"}, {"versioned_ensembl_gene_id":"ENSG00000174353.17","gene_symbol":"STAG3L3","gene_name":"stromal antigen 3-like 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33845]","synonyms":"STAG3L3P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442578","summary":null,"start":72969696,"end":73005922,"strand":-1,"description":"stromal antigen 3-like 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33845]"}, {"versioned_ensembl_gene_id":"ENSG00000204511.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31528717,"end":31530232,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000182472.8","gene_symbol":"CAPN12","gene_name":"calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147968","summary":"The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes a member of the calpain large subunit family. [provided by RefSeq, Jun 2012]","start":38730187,"end":38769904,"strand":-1,"description":"calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]"}, {"versioned_ensembl_gene_id":"ENSG00000164902.13","gene_symbol":"PHAX","gene_name":"phosphorylated adaptor for RNA export [Source:HGNC Symbol;Acc:HGNC:10241]","synonyms":"RNUXA,FLJ13193","biotype":"protein_coding","ncbi_id":"51808","summary":null,"start":126600268,"end":126627252,"strand":1,"description":"phosphorylated adaptor for RNA export [Source:HGNC Symbol;Acc:HGNC:10241]"}, {"versioned_ensembl_gene_id":"ENSG00000231489.1","gene_symbol":"AL606490.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48423342,"end":48423468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283669.1","gene_symbol":"AC112487.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":112321140,"end":112321443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274244.1","gene_symbol":"AC243585.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37649133,"end":37650894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254669.1","gene_symbol":"AL135934.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35579430,"end":35585310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268201.1","gene_symbol":"AC020915.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58266635,"end":58267685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119280.16","gene_symbol":"C1orf198","gene_name":"chromosome 1 open reading frame 198 [Source:HGNC Symbol;Acc:HGNC:25900]","synonyms":"FLJ14525,DKFZp667D152,MGC10710,FLJ38847,FLJ16283","biotype":"protein_coding","ncbi_id":"84886","summary":null,"start":230837119,"end":230869589,"strand":-1,"description":"chromosome 1 open reading frame 198 [Source:HGNC Symbol;Acc:HGNC:25900]"}, {"versioned_ensembl_gene_id":"ENSG00000225656.1","gene_symbol":"AL118511.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":230823641,"end":230824707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184060.10","gene_symbol":"ADAP2","gene_name":"ArfGAP with dual PH domains 2 [Source:HGNC Symbol;Acc:HGNC:16487]","synonyms":"CENTA2","biotype":"protein_coding","ncbi_id":"55803","summary":"The protein encoded by this gene binds beta-tubulin and increases the stability of microtubules. The encoded protein can also translocate to the cell membrane and bind phosphatidylinositol 3,4,5-trisphosphate (PtdInsP3) and inositol 1,3,4,5-tetrakisphosphate (InsP4). In addition, this protein is a GTPase-activating protein for ADP ribosylation factor 6 and may be able to block the entry of some RNA viruses. [provided by RefSeq, Oct 2016]","start":30906344,"end":30959322,"strand":1,"description":"ArfGAP with dual PH domains 2 [Source:HGNC Symbol;Acc:HGNC:16487]"}, {"versioned_ensembl_gene_id":"ENSG00000219797.2","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31519480,"end":31520291,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000224544.2","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31130046,"end":31131862,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000279357.1","gene_symbol":"AC007224.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8666762,"end":8667271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170089.15","gene_symbol":"AC106795.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":177809407,"end":177950732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237421.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464664,"end":29469874,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000092208.16","gene_symbol":"GEMIN2","gene_name":"gem nuclear organelle associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10884]","synonyms":"SIP1","biotype":"protein_coding","ncbi_id":"8487","summary":"This gene encodes one of the proteins found in the SMN complex, which consists of several gemin proteins and the protein known as the survival of motor neuron protein. The SMN complex is localized to a subnuclear compartment called gems (gemini of coiled bodies) and is required for assembly of spliceosomal snRNPs and for pre-mRNA splicing. This protein interacts directly with the survival of motor neuron protein and it is required for formation of the SMN complex. A knockout mouse targeting the mouse homolog of this gene exhibited disrupted snRNP assembly and motor neuron degeneration. [provided by RefSeq, Aug 2011]","start":39114223,"end":39136973,"strand":1,"description":"gem nuclear organelle associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10884]"}, {"versioned_ensembl_gene_id":"ENSG00000249849.1","gene_symbol":"AC138819.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177682294,"end":177713969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238234.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"PBMUCL2,FLJ37114","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31046568,"end":31052373,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000224409.1","gene_symbol":"AC114489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32717734,"end":32725237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225092.2","gene_symbol":"AL355336.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7183083,"end":7185287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231528.2","gene_symbol":"FAM225A","gene_name":"family with sequence similarity 225 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27855]","synonyms":"NCRNA00256A,LINC00256A,DKFZp686A0127,C9orf109","biotype":"lincRNA","ncbi_id":"286333","summary":null,"start":113113073,"end":113119928,"strand":1,"description":"family with sequence similarity 225 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27855]"}, {"versioned_ensembl_gene_id":"ENSG00000250135.1","gene_symbol":"AL049795.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32170733,"end":32176568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273321.1","gene_symbol":"AC023983.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24402153,"end":24402714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170465.9","gene_symbol":"KRT6C","gene_name":"keratin 6C [Source:HGNC Symbol;Acc:HGNC:20406]","synonyms":"KRT6E","biotype":"protein_coding","ncbi_id":"286887","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. The type II keratins are clustered in a region of chromosome 12q13. [provided by RefSeq, Jul 2009]","start":52468516,"end":52473785,"strand":-1,"description":"keratin 6C [Source:HGNC Symbol;Acc:HGNC:20406]"}, {"versioned_ensembl_gene_id":"ENSG00000160460.15","gene_symbol":"SPTBN4","gene_name":"spectrin beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:HGNC:14896]","synonyms":"SPTBN3,KIAA1642","biotype":"protein_coding","ncbi_id":"57731","summary":"Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is composed of two antiparallel dimers of alpha- and beta- subunits. This gene is one member of a family of beta-spectrin genes. The encoded protein localizes to the nuclear matrix, PML nuclear bodies, and cytoplasmic vesicles. A highly similar gene in the mouse is required for localization of specific membrane proteins in polarized regions of neurons. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":40466241,"end":40576464,"strand":1,"description":"spectrin beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:HGNC:14896]"}, {"versioned_ensembl_gene_id":"ENSG00000177374.12","gene_symbol":"HIC1","gene_name":"HIC ZBTB transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:4909]","synonyms":"ZNF901,ZBTB29","biotype":"protein_coding","ncbi_id":"3090","summary":"This gene functions as a growth regulatory and tumor repressor gene. Hypermethylation or deletion of the region of this gene have been associated with tumors and the contiguous-gene syndrome, Miller-Dieker syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":2054154,"end":2063241,"strand":1,"description":"HIC ZBTB transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:4909]"}, {"versioned_ensembl_gene_id":"ENSG00000234137.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":30973408,"end":30979603,"strand":1,"description":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]"}, {"versioned_ensembl_gene_id":"ENSG00000234063.5","gene_symbol":"AL663093.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31000184,"end":31025215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233377.1","gene_symbol":"MTND4P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42207]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873352","summary":null,"start":94940253,"end":94941121,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42207]"}, {"versioned_ensembl_gene_id":"ENSG00000124102.4","gene_symbol":"PI3","gene_name":"peptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:8947]","synonyms":"WFDC14,WAP3,SKALP,ESI,ELAFIN,cementoin","biotype":"protein_coding","ncbi_id":"5266","summary":"This gene encodes an elastase-specific inhibitor that functions as an antimicrobial peptide against Gram-positive and Gram-negative bacteria, and fungal pathogens. The protein contains a WAP-type four-disulfide core (WFDC) domain, and is thus a member of the WFDC domain family. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. Expression of this gene is upgulated by bacterial lipopolysaccharides and cytokines. [provided by RefSeq, Oct 2014]","start":45174876,"end":45176544,"strand":1,"description":"peptidase inhibitor 3 [Source:HGNC Symbol;Acc:HGNC:8947]"}, {"versioned_ensembl_gene_id":"ENSG00000142583.17","gene_symbol":"SLC2A5","gene_name":"solute carrier family 2 member 5 [Source:HGNC Symbol;Acc:HGNC:11010]","synonyms":"GLUT5","biotype":"protein_coding","ncbi_id":"6518","summary":"The protein encoded by this gene is a fructose transporter responsible for fructose uptake by the small intestine. The encoded protein also is necessary for the increase in blood pressure due to high dietary fructose consumption. [provided by RefSeq, Jun 2016]","start":9035107,"end":9088478,"strand":-1,"description":"solute carrier family 2 member 5 [Source:HGNC Symbol;Acc:HGNC:11010]"}, {"versioned_ensembl_gene_id":"ENSG00000267114.1","gene_symbol":"AC011481.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44950044,"end":44954007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256450.1","gene_symbol":"AC007552.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16513445,"end":16514371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112337.10","gene_symbol":"SLC17A2","gene_name":"solute carrier family 17 member 2 [Source:HGNC Symbol;Acc:HGNC:10930]","synonyms":"NPT3","biotype":"protein_coding","ncbi_id":"10246","summary":null,"start":25912754,"end":25930726,"strand":-1,"description":"solute carrier family 17 member 2 [Source:HGNC Symbol;Acc:HGNC:10930]"}, {"versioned_ensembl_gene_id":"ENSG00000227969.1","gene_symbol":"NPM1P22","gene_name":"nucleophosmin 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39679]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390411","summary":null,"start":67831876,"end":67832827,"strand":-1,"description":"nucleophosmin 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39679]"}, {"versioned_ensembl_gene_id":"ENSG00000260532.1","gene_symbol":"AL031598.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1111627,"end":1113399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243926.1","gene_symbol":"TIPARP-AS1","gene_name":"TIPARP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41028]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287227","summary":null,"start":156671862,"end":156674378,"strand":-1,"description":"TIPARP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41028]"}, {"versioned_ensembl_gene_id":"ENSG00000231667.2","gene_symbol":"OR7E111P","gene_name":"olfactory receptor family 7 subfamily E member 111 pseudogene [Source:HGNC Symbol;Acc:HGNC:15344]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81136","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":67902208,"end":67903221,"strand":1,"description":"olfactory receptor family 7 subfamily E member 111 pseudogene [Source:HGNC Symbol;Acc:HGNC:15344]"}, {"versioned_ensembl_gene_id":"ENSG00000273551.1","gene_symbol":"AC120498.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1148224,"end":1148754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163659.12","gene_symbol":"TIPARP","gene_name":"TCDD inducible poly(ADP-ribose) polymerase [Source:HGNC Symbol;Acc:HGNC:23696]","synonyms":"DKFZP434J214,DDF1,RM1,pART14,PARP7,PARP-7,PARP-1,DKFZp686N0351","biotype":"protein_coding","ncbi_id":"25976","summary":"This gene encodes a member of the poly(ADP-ribose) polymerase superfamily. Studies of the mouse ortholog have shown that the encoded protein catalyzes histone poly(ADP-ribosyl)ation and may be involved in T-cell function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":156673235,"end":156706770,"strand":1,"description":"TCDD inducible poly(ADP-ribose) polymerase [Source:HGNC Symbol;Acc:HGNC:23696]"}, {"versioned_ensembl_gene_id":"ENSG00000124233.11","gene_symbol":"SEMG1","gene_name":"semenogelin I [Source:HGNC Symbol;Acc:HGNC:10742]","synonyms":"SEMG,CT103","biotype":"protein_coding","ncbi_id":"6406","summary":"The protein encoded by this gene is the predominant protein in semen. The encoded secreted protein is involved in the formation of a gel matrix that encases ejaculated spermatozoa. This preproprotein is proteolytically processed by the prostate-specific antigen (PSA) protease to generate multiple peptide products that exhibit distinct functions. One of these peptides, SgI-29, is an antimicrobial peptide with antibacterial activity. This proteolysis process also breaks down the gel matrix and allows the spermatozoa to move more freely. This gene and another similar semenogelin gene are present in a gene cluster on chromosome 20. [provided by RefSeq, Feb 2016]","start":45206997,"end":45209772,"strand":1,"description":"semenogelin I [Source:HGNC Symbol;Acc:HGNC:10742]"}, {"versioned_ensembl_gene_id":"ENSG00000233757.6","gene_symbol":"AC092835.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":95207535,"end":95259774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168306.12","gene_symbol":"ACOX2","gene_name":"acyl-CoA oxidase 2 [Source:HGNC Symbol;Acc:HGNC:120]","synonyms":"THCCox,BRCOX,BRCACOX","biotype":"protein_coding","ncbi_id":"8309","summary":"The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe cognitive disability, and death in children. [provided by RefSeq, Mar 2009]","start":58505136,"end":58537319,"strand":-1,"description":"acyl-CoA oxidase 2 [Source:HGNC Symbol;Acc:HGNC:120]"}, {"versioned_ensembl_gene_id":"ENSG00000229525.1","gene_symbol":"AC053503.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219388496,"end":219403633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228907.5","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"G16,RING5,RMA1,NG2","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32217742,"end":32220181,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000271290.1","gene_symbol":"AL390058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86798598,"end":86799226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123992.18","gene_symbol":"DNPEP","gene_name":"aspartyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:2981]","synonyms":"DAP,ASPEP","biotype":"protein_coding","ncbi_id":"23549","summary":"The protein encoded by this gene is an aminopeptidase which prefers acidic amino acids, and specifically favors aspartic acid over glutamic acid. It is thought to be a cytosolic protein involved in general metabolism of intracellular proteins. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":219373546,"end":219400022,"strand":-1,"description":"aspartyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:2981]"}, {"versioned_ensembl_gene_id":"ENSG00000261145.1","gene_symbol":"AC009060.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70202354,"end":70202459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229386.3","gene_symbol":"OR8B9P","gene_name":"olfactory receptor family 8 subfamily B member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:14746]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79316","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124476963,"end":124482870,"strand":-1,"description":"olfactory receptor family 8 subfamily B member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:14746]"}, {"versioned_ensembl_gene_id":"ENSG00000156218.12","gene_symbol":"ADAMTSL3","gene_name":"ADAMTS like 3 [Source:HGNC Symbol;Acc:HGNC:14633]","synonyms":"punctin-2,KIAA1233","biotype":"protein_coding","ncbi_id":"57188","summary":null,"start":83654086,"end":84039842,"strand":1,"description":"ADAMTS like 3 [Source:HGNC Symbol;Acc:HGNC:14633]"}, {"versioned_ensembl_gene_id":"ENSG00000144285.18","gene_symbol":"SCN1A","gene_name":"sodium voltage-gated channel alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:10585]","synonyms":"Nav1.1,NAC1,HBSCI,GEFSP2,FEB3,SMEI,SCN1","biotype":"protein_coding","ncbi_id":"6323","summary":"Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015]","start":165984641,"end":166149214,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:10585]"}, {"versioned_ensembl_gene_id":"ENSG00000264659.1","gene_symbol":"AC064805.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74672712,"end":74677600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134058.11","gene_symbol":"CDK7","gene_name":"cyclin dependent kinase 7 [Source:HGNC Symbol;Acc:HGNC:1778]","synonyms":"CDKN7,CAK1,CAK,STK1,MO15","biotype":"protein_coding","ncbi_id":"1022","summary":"The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of Saccharomyces cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, and are known to be important regulators of cell cycle progression. This protein forms a trimeric complex with cyclin H and MAT1, which functions as a Cdk-activating kinase (CAK). It is an essential component of the transcription factor TFIIH, that is involved in transcription initiation and DNA repair. This protein is thought to serve as a direct link between the regulation of transcription and the cell cycle. [provided by RefSeq, Jul 2008]","start":69234795,"end":69277430,"strand":1,"description":"cyclin dependent kinase 7 [Source:HGNC Symbol;Acc:HGNC:1778]"}, {"versioned_ensembl_gene_id":"ENSG00000087086.14","gene_symbol":"FTL","gene_name":"ferritin light chain [Source:HGNC Symbol;Acc:HGNC:3999]","synonyms":"MGC71996,NBIA3","biotype":"protein_coding","ncbi_id":"2512","summary":"This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes. [provided by RefSeq, Jul 2008]","start":48965301,"end":48966878,"strand":1,"description":"ferritin light chain [Source:HGNC Symbol;Acc:HGNC:3999]"}, {"versioned_ensembl_gene_id":"ENSG00000176845.12","gene_symbol":"METRNL","gene_name":"meteorin like, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:27584]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284207","summary":null,"start":83079691,"end":83095119,"strand":1,"description":"meteorin like, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:27584]"}, {"versioned_ensembl_gene_id":"ENSG00000229010.1","gene_symbol":"AL161672.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23140325,"end":23141142,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053501.12","gene_symbol":"USE1","gene_name":"unconventional SNARE in the ER 1 [Source:HGNC Symbol;Acc:HGNC:30882]","synonyms":"SLT1,p31,MDS032,D12","biotype":"protein_coding","ncbi_id":"55850","summary":null,"start":17215346,"end":17219829,"strand":1,"description":"unconventional SNARE in the ER 1 [Source:HGNC Symbol;Acc:HGNC:30882]"}, {"versioned_ensembl_gene_id":"ENSG00000259294.1","gene_symbol":"AC005096.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101822247,"end":101824729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264031.1","gene_symbol":"ABHD15-AS1","gene_name":"ABHD15 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49685]","synonyms":"lnc-TP53I13,linc-TP53I13","biotype":"antisense_RNA","ncbi_id":"104355133","summary":null,"start":29560547,"end":29707090,"strand":1,"description":"ABHD15 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49685]"}, {"versioned_ensembl_gene_id":"ENSG00000137821.11","gene_symbol":"LRRC49","gene_name":"leucine rich repeat containing 49 [Source:HGNC Symbol;Acc:HGNC:25965]","synonyms":"FLJ20156","biotype":"protein_coding","ncbi_id":"54839","summary":null,"start":70853239,"end":71053657,"strand":1,"description":"leucine rich repeat containing 49 [Source:HGNC Symbol;Acc:HGNC:25965]"}, {"versioned_ensembl_gene_id":"ENSG00000262402.1","gene_symbol":"AC090617.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2127430,"end":2127904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215365.4","gene_symbol":"FAM90A22P","gene_name":"family with sequence similarity 90 member A22, pseudogene [Source:HGNC Symbol;Acc:HGNC:32270]","synonyms":"FAM90A22","biotype":"unprocessed_pseudogene","ncbi_id":"645558","summary":null,"start":7571995,"end":7575006,"strand":-1,"description":"family with sequence similarity 90 member A22, pseudogene [Source:HGNC Symbol;Acc:HGNC:32270]"}, {"versioned_ensembl_gene_id":"ENSG00000258635.1","gene_symbol":"CR354443.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31746360,"end":31757371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131981.15","gene_symbol":"LGALS3","gene_name":"galectin 3 [Source:HGNC Symbol;Acc:HGNC:6563]","synonyms":"MAC-2,LGALS2,GALIG","biotype":"protein_coding","ncbi_id":"3958","summary":"This gene encodes a member of the galectin family of carbohydrate binding proteins. Members of this protein family have an affinity for beta-galactosides. The encoded protein is characterized by an N-terminal proline-rich tandem repeat domain and a single C-terminal carbohydrate recognition domain. This protein can self-associate through the N-terminal domain allowing it to bind to multivalent saccharide ligands. This protein localizes to the extracellular matrix, the cytoplasm and the nucleus. This protein plays a role in numerous cellular functions including apoptosis, innate immunity, cell adhesion and T-cell regulation. The protein exhibits antimicrobial activity against bacteria and fungi. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2014]","start":55124110,"end":55145413,"strand":1,"description":"galectin 3 [Source:HGNC Symbol;Acc:HGNC:6563]"}, {"versioned_ensembl_gene_id":"ENSG00000187103.3","gene_symbol":"FUNDC2P3","gene_name":"FUN14 domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644625","summary":null,"start":146171315,"end":146171847,"strand":1,"description":"FUN14 domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37970]"}, {"versioned_ensembl_gene_id":"ENSG00000104941.7","gene_symbol":"RSPH6A","gene_name":"radial spoke head 6 homolog A [Source:HGNC Symbol;Acc:HGNC:14241]","synonyms":"RSPH4B,RSP6,RSP4,RSHL1","biotype":"protein_coding","ncbi_id":"81492","summary":"The protein encoded by this gene is similar to a sea urchin radial spoke head protein. Radial spoke protein complexes form part of the axoneme of eukaryotic flagella and are located between the axoneme's outer ring of doublet microtubules and central pair of microtubules. In Chlamydomonas, radial spoke proteins are thought to regulate the activity of dynein and the symmetry of flagellar bending patterns. This gene maps to a region of chromosome 19 that is linked to primary ciliary dyskinesia-2 (CILD2). [provided by RefSeq, Jul 2008]","start":45795710,"end":45815319,"strand":-1,"description":"radial spoke head 6 homolog A [Source:HGNC Symbol;Acc:HGNC:14241]"}, {"versioned_ensembl_gene_id":"ENSG00000269604.1","gene_symbol":"AC005523.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4791745,"end":4795559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212724.3","gene_symbol":"KRTAP2-3","gene_name":"keratin associated protein 2-3 [Source:HGNC Symbol;Acc:HGNC:18906]","synonyms":"KAP2.3","biotype":"protein_coding","ncbi_id":"730755","summary":null,"start":41059240,"end":41060114,"strand":-1,"description":"keratin associated protein 2-3 [Source:HGNC Symbol;Acc:HGNC:18906]"}, {"versioned_ensembl_gene_id":"ENSG00000135409.10","gene_symbol":"AMHR2","gene_name":"anti-Mullerian hormone receptor type 2 [Source:HGNC Symbol;Acc:HGNC:465]","synonyms":"MISRII,MISR2","biotype":"protein_coding","ncbi_id":"269","summary":"This gene encodes the receptor for the anti-Mullerian hormone (AMH) which, in addition to testosterone, results in male sex differentiation. AMH and testosterone are produced in the testes by different cells and have different effects. Testosterone promotes the development of male genitalia while the binding of AMH to the encoded receptor prevents the development of the mullerian ducts into uterus and Fallopian tubes. Mutations in this gene are associated with persistent Mullerian duct syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2009]","start":53423855,"end":53431534,"strand":1,"description":"anti-Mullerian hormone receptor type 2 [Source:HGNC Symbol;Acc:HGNC:465]"}, {"versioned_ensembl_gene_id":"ENSG00000204361.8","gene_symbol":"NXPE2","gene_name":"neurexophilin and PC-esterase domain family member 2 [Source:HGNC Symbol;Acc:HGNC:26331]","synonyms":"FLJ25224,FAM55B","biotype":"protein_coding","ncbi_id":"120406","summary":null,"start":114678386,"end":114706933,"strand":1,"description":"neurexophilin and PC-esterase domain family member 2 [Source:HGNC Symbol;Acc:HGNC:26331]"}, {"versioned_ensembl_gene_id":"ENSG00000261474.1","gene_symbol":"AC026471.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31449535,"end":31453493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254656.1","gene_symbol":"RTL1","gene_name":"retrotransposon Gag like 1 [Source:HGNC Symbol;Acc:HGNC:14665]","synonyms":"SIRH2,PEG11,MART1,Mar1,HUR1","biotype":"protein_coding","ncbi_id":"388015","summary":"This gene is a retrotransposon-derived, paternally expressed imprinted gene that is highly expressed at the late fetal stage in both the fetus and placenta. It has an overlapping maternally expressed antisense transcript, which contains several microRNAs targeting the transcripts of this gene through an RNA interference (RNAi) mechanism. This gene is essential for maintenance of the fetal capillaries. [provided by RefSeq, Jul 2009]","start":100880655,"end":100884847,"strand":-1,"description":"retrotransposon Gag like 1 [Source:HGNC Symbol;Acc:HGNC:14665]"}, {"versioned_ensembl_gene_id":"ENSG00000140093.9","gene_symbol":"SERPINA10","gene_name":"serpin family A member 10 [Source:HGNC Symbol;Acc:HGNC:15996]","synonyms":"ZPI,PZI","biotype":"protein_coding","ncbi_id":"51156","summary":"The protein encoded by this gene belongs to the serpin family. It is predominantly expressed in the liver and secreted in plasma. It inhibits the activity of coagulation factors Xa and XIa in the presence of protein Z, calcium and phospholipid. Mutations in this gene are associated with venous thrombosis. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, May 2010]","start":94280455,"end":94293271,"strand":-1,"description":"serpin family A member 10 [Source:HGNC Symbol;Acc:HGNC:15996]"}, {"versioned_ensembl_gene_id":"ENSG00000188581.8","gene_symbol":"KRTAP1-1","gene_name":"keratin associated protein 1-1 [Source:HGNC Symbol;Acc:HGNC:16772]","synonyms":"HB2A,KAP1.1B,KAP1.1A,KAP1.1","biotype":"protein_coding","ncbi_id":"81851","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41040559,"end":41041461,"strand":-1,"description":"keratin associated protein 1-1 [Source:HGNC Symbol;Acc:HGNC:16772]"}, {"versioned_ensembl_gene_id":"ENSG00000250441.1","gene_symbol":"AC109481.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108894347,"end":108894628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253165.1","gene_symbol":"AC090821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133775551,"end":133777352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110002.15","gene_symbol":"VWA5A","gene_name":"von Willebrand factor A domain containing 5A [Source:HGNC Symbol;Acc:HGNC:6658]","synonyms":"LOH11CR2A,BCSC-1","biotype":"protein_coding","ncbi_id":"4013","summary":null,"start":124115362,"end":124147721,"strand":1,"description":"von Willebrand factor A domain containing 5A [Source:HGNC Symbol;Acc:HGNC:6658]"}, {"versioned_ensembl_gene_id":"ENSG00000271098.1","gene_symbol":"IMMP1LP3","gene_name":"inner mitochondrial membrane peptidase subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481715","summary":null,"start":2287915,"end":2288428,"strand":1,"description":"inner mitochondrial membrane peptidase subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51134]"}, {"versioned_ensembl_gene_id":"ENSG00000165325.13","gene_symbol":"DEUP1","gene_name":"deuterosome assembly protein 1 [Source:HGNC Symbol;Acc:HGNC:26344]","synonyms":"FLJ25393,CCDC67","biotype":"protein_coding","ncbi_id":"159989","summary":null,"start":93329971,"end":93438487,"strand":1,"description":"deuterosome assembly protein 1 [Source:HGNC Symbol;Acc:HGNC:26344]"}, {"versioned_ensembl_gene_id":"ENSG00000242640.1","gene_symbol":"RPS29P11","gene_name":"ribosomal protein S29 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36413]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129902","summary":null,"start":25678850,"end":25679020,"strand":1,"description":"ribosomal protein S29 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36413]"}, {"versioned_ensembl_gene_id":"ENSG00000275597.1","gene_symbol":"AC108479.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87980714,"end":87992858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247699.2","gene_symbol":"AC008609.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160195744,"end":160204826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233205.1","gene_symbol":"AC108479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87972656,"end":87973082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227868.5","gene_symbol":"TEX46","gene_name":"testis expressed 46 [Source:HGNC Symbol;Acc:HGNC:44651]","synonyms":"TEX#,C1orf234","biotype":"protein_coding","ncbi_id":"729059","summary":null,"start":23010834,"end":23015850,"strand":-1,"description":"testis expressed 46 [Source:HGNC Symbol;Acc:HGNC:44651]"}, {"versioned_ensembl_gene_id":"ENSG00000225471.5","gene_symbol":"BX119917.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":72159845,"end":72160346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254852.8","gene_symbol":"NPIPA2","gene_name":"nuclear pore complex interacting protein family member A2 [Source:HGNC Symbol;Acc:HGNC:41979]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642799","summary":null,"start":14748066,"end":14765413,"strand":1,"description":"nuclear pore complex interacting protein family member A2 [Source:HGNC Symbol;Acc:HGNC:41979]"}, {"versioned_ensembl_gene_id":"ENSG00000213182.4","gene_symbol":"OR10D5P","gene_name":"olfactory receptor family 10 subfamily D member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14838]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79488","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":124054793,"end":124055707,"strand":1,"description":"olfactory receptor family 10 subfamily D member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:14838]"}, {"versioned_ensembl_gene_id":"ENSG00000143740.14","gene_symbol":"SNAP47","gene_name":"synaptosome associated protein 47 [Source:HGNC Symbol;Acc:HGNC:30669]","synonyms":"SVAP1,SNAP-47,C1orf142","biotype":"protein_coding","ncbi_id":"116841","summary":null,"start":227728539,"end":227781231,"strand":1,"description":"synaptosome associated protein 47 [Source:HGNC Symbol;Acc:HGNC:30669]"}, {"versioned_ensembl_gene_id":"ENSG00000261090.1","gene_symbol":"AC127459.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23020337,"end":23023611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146409.10","gene_symbol":"SLC18B1","gene_name":"solute carrier family 18 member B1 [Source:HGNC Symbol;Acc:HGNC:21573]","synonyms":"dJ55C23.6,C6orf192","biotype":"protein_coding","ncbi_id":"116843","summary":"This gene encodes a protein, which has high sequence similarity to rat, xenopus and zebrafish proteins. The protein function is unknown. [provided by RefSeq, Jul 2008]","start":132769370,"end":132798553,"strand":-1,"description":"solute carrier family 18 member B1 [Source:HGNC Symbol;Acc:HGNC:21573]"}, {"versioned_ensembl_gene_id":"ENSG00000266987.1","gene_symbol":"AC104984.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30144062,"end":30144790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233110.1","gene_symbol":"AC093797.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185587909,"end":185594003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177354.11","gene_symbol":"C10orf71","gene_name":"chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:26973]","synonyms":"FLJ45913","biotype":"protein_coding","ncbi_id":"118461","summary":null,"start":49299193,"end":49327487,"strand":1,"description":"chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:26973]"}, {"versioned_ensembl_gene_id":"ENSG00000244731.7","gene_symbol":"C4A","gene_name":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]","synonyms":"C4A2,C4A6,CO4,C4,C4A4,C4S,RG,C4A3,C4B,CPAMD2","biotype":"protein_coding","ncbi_id":"720","summary":"This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain is cleaved to release C4 anaphylatoxin, an antimicrobial peptide and a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":31982024,"end":32002681,"strand":1,"description":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]"}, {"versioned_ensembl_gene_id":"ENSG00000233627.2","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478955","summary":null,"start":31999976,"end":32003521,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000145901.14","gene_symbol":"TNIP1","gene_name":"TNFAIP3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16903]","synonyms":"KIAA0113,ABIN-1,VAN,NAF1","biotype":"protein_coding","ncbi_id":"10318","summary":"This gene encodes an A20-binding protein which plays a role in autoimmunity and tissue homeostasis through the regulation of nuclear factor kappa-B activation. Mutations in this gene have been associated with psoriatic arthritis, rheumatoid arthritis, and systemic lupus erythematosus. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":151029945,"end":151093577,"strand":-1,"description":"TNFAIP3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16903]"}, {"versioned_ensembl_gene_id":"ENSG00000167543.15","gene_symbol":"TP53I13","gene_name":"tumor protein p53 inducible protein 13 [Source:HGNC Symbol;Acc:HGNC:25102]","synonyms":"DSCP1","biotype":"protein_coding","ncbi_id":"90313","summary":null,"start":29566052,"end":29573157,"strand":1,"description":"tumor protein p53 inducible protein 13 [Source:HGNC Symbol;Acc:HGNC:25102]"}, {"versioned_ensembl_gene_id":"ENSG00000152904.11","gene_symbol":"GGPS1","gene_name":"geranylgeranyl diphosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:4249]","synonyms":"GGPPS1","biotype":"protein_coding","ncbi_id":"9453","summary":"This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor. Alternate transcriptional splice variants, both protein-coding and non-protein-coding, have been found for this gene. [provided by RefSeq, Sep 2010]","start":235327350,"end":235344532,"strand":1,"description":"geranylgeranyl diphosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:4249]"}, {"versioned_ensembl_gene_id":"ENSG00000265394.1","gene_symbol":"AC104984.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30090366,"end":30117497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163697.16","gene_symbol":"APBB2","gene_name":"amyloid beta precursor protein binding family B member 2 [Source:HGNC Symbol;Acc:HGNC:582]","synonyms":"FE65L1,FE65L,MGC35575","biotype":"protein_coding","ncbi_id":"323","summary":"The protein encoded by this gene interacts with the cytoplasmic domains of amyloid beta (A4) precursor protein and amyloid beta (A4) precursor-like protein 2. This protein contains two phosphotyrosine binding (PTB) domains, which are thought to function in signal transduction. Polymorphisms in this gene have been associated with Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":40810027,"end":41216714,"strand":-1,"description":"amyloid beta precursor protein binding family B member 2 [Source:HGNC Symbol;Acc:HGNC:582]"}, {"versioned_ensembl_gene_id":"ENSG00000141540.10","gene_symbol":"TTYH2","gene_name":"tweety family member 2 [Source:HGNC Symbol;Acc:HGNC:13877]","synonyms":"C17orf29","biotype":"protein_coding","ncbi_id":"94015","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-activated large conductance chloride(-) channel, and may play a role in kidney tumorigenesis. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":74213514,"end":74262020,"strand":1,"description":"tweety family member 2 [Source:HGNC Symbol;Acc:HGNC:13877]"}, {"versioned_ensembl_gene_id":"ENSG00000262410.1","gene_symbol":"AC024361.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":82745068,"end":82745709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137634.9","gene_symbol":"NXPE4","gene_name":"neurexophilin and PC-esterase domain family member 4 [Source:HGNC Symbol;Acc:HGNC:23117]","synonyms":"FLJ20127,FAM55D,C11orf33","biotype":"protein_coding","ncbi_id":"54827","summary":null,"start":114570591,"end":114595762,"strand":-1,"description":"neurexophilin and PC-esterase domain family member 4 [Source:HGNC Symbol;Acc:HGNC:23117]"}, {"versioned_ensembl_gene_id":"ENSG00000131043.11","gene_symbol":"AAR2","gene_name":"AAR2 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:15886]","synonyms":"C20orf4,bA234K24.2","biotype":"protein_coding","ncbi_id":"25980","summary":"This gene encodes the homolog of the yeast A1-alpha2 repressin protein that is involved in mRNA splicing. Alternately spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]","start":36236459,"end":36270918,"strand":1,"description":"AAR2 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:15886]"}, {"versioned_ensembl_gene_id":"ENSG00000180008.8","gene_symbol":"SOCS4","gene_name":"suppressor of cytokine signaling 4 [Source:HGNC Symbol;Acc:HGNC:19392]","synonyms":"SOCS7","biotype":"protein_coding","ncbi_id":"122809","summary":"The protein encoded by this gene contains a SH2 domain and a SOCS BOX domain. The protein thus belongs to the suppressor of cytokine signaling (SOCS), also known as STAT-induced STAT inhibitor (SSI), protein family. SOCS family members are known to be cytokine-inducible negative regulators of cytokine signaling. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":55027230,"end":55049488,"strand":1,"description":"suppressor of cytokine signaling 4 [Source:HGNC Symbol;Acc:HGNC:19392]"}, {"versioned_ensembl_gene_id":"ENSG00000141542.10","gene_symbol":"RAB40B","gene_name":"RAB40B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18284]","synonyms":"SEC4L,RAR","biotype":"protein_coding","ncbi_id":"10966","summary":"The protein encoded by this gene has similarity to a yeast protein which suggests a role of the gene product in regulating secretory vesicles. [provided by RefSeq, Jul 2008]","start":82654973,"end":82698728,"strand":-1,"description":"RAB40B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18284]"}, {"versioned_ensembl_gene_id":"ENSG00000188060.7","gene_symbol":"RAB42","gene_name":"RAB42, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:28702]","synonyms":"MGC45806","biotype":"protein_coding","ncbi_id":"115273","summary":null,"start":28592200,"end":28595443,"strand":1,"description":"RAB42, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:28702]"}, {"versioned_ensembl_gene_id":"ENSG00000262147.1","gene_symbol":"AC124283.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82587313,"end":82588411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230741.1","gene_symbol":"Z82173.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33320865,"end":33322813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260988.1","gene_symbol":"AC090260.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78141243,"end":78143173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254697.1","gene_symbol":"COPS8P3","gene_name":"COP9 signalosome subunit 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45271]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479058","summary":null,"start":78581675,"end":78582156,"strand":1,"description":"COP9 signalosome subunit 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45271]"}, {"versioned_ensembl_gene_id":"ENSG00000069188.16","gene_symbol":"SDK2","gene_name":"sidekick cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:19308]","synonyms":"KIAA1514,FLJ10832","biotype":"protein_coding","ncbi_id":"54549","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains two immunoglobulin domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. This protein, and a homologous mouse sequence, are very similar to the Drosophila sidekick gene product but the specific function of this superfamily member is not yet known. Evidence for alternative splicing at this gene locus has been observed but the full-length nature of additional variants has not yet been determined. [provided by RefSeq, Jul 2008]","start":73334384,"end":73644089,"strand":-1,"description":"sidekick cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:19308]"}, {"versioned_ensembl_gene_id":"ENSG00000229215.9","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29881755,"end":30002076,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000270400.1","gene_symbol":"AL512782.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83145540,"end":83145903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233503.1","gene_symbol":"HNRNPLP1","gene_name":"heterogeneous nuclear ribonucleoprotein L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48748]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442157","summary":null,"start":7481094,"end":7482594,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48748]"}, {"versioned_ensembl_gene_id":"ENSG00000236262.1","gene_symbol":"SHANK2-AS2","gene_name":"SHANK2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40015]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874199","summary":null,"start":70646165,"end":70647562,"strand":1,"description":"SHANK2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40015]"}, {"versioned_ensembl_gene_id":"ENSG00000171671.6","gene_symbol":"SHANK2-AS3","gene_name":"SHANK2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:25098]","synonyms":"C11orf76","biotype":"antisense_RNA","ncbi_id":"220070","summary":null,"start":70862790,"end":70865115,"strand":1,"description":"SHANK2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:25098]"}, {"versioned_ensembl_gene_id":"ENSG00000280089.1","gene_symbol":"AP000590.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70705605,"end":70706068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225934.2","gene_symbol":"AL592310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227598424,"end":227599094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138780.14","gene_symbol":"GSTCD","gene_name":"glutathione S-transferase C-terminal domain containing [Source:HGNC Symbol;Acc:HGNC:25806]","synonyms":"FLJ13273","biotype":"protein_coding","ncbi_id":"79807","summary":null,"start":105708778,"end":105847728,"strand":1,"description":"glutathione S-transferase C-terminal domain containing [Source:HGNC Symbol;Acc:HGNC:25806]"}, {"versioned_ensembl_gene_id":"ENSG00000147604.13","gene_symbol":"RPL7","gene_name":"ribosomal protein L7 [Source:HGNC Symbol;Acc:HGNC:10363]","synonyms":"L7,humL7-1","biotype":"protein_coding","ncbi_id":"6129","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L30P family of ribosomal proteins. It contains an N-terminal basic region-leucine zipper (BZIP)-like domain and the RNP consensus submotif RNP2. In vitro the BZIP-like domain mediates homodimerization and stable binding to DNA and RNA, with a preference for 28S rRNA and mRNA. The protein can inhibit cell-free translation of mRNAs, suggesting that it plays a regulatory role in the translation apparatus. It is located in the cytoplasm. The protein has been shown to be an autoantigen in patients with systemic autoimmune diseases, such as systemic lupus erythematosus. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":73290267,"end":73295789,"strand":-1,"description":"ribosomal protein L7 [Source:HGNC Symbol;Acc:HGNC:10363]"}, {"versioned_ensembl_gene_id":"ENSG00000081842.17","gene_symbol":"PCDHA6","gene_name":"protocadherin alpha 6 [Source:HGNC Symbol;Acc:HGNC:8672]","synonyms":"PCDH-ALPHA6,CRNR2,CNRS2,CNR2","biotype":"protein_coding","ncbi_id":"56142","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140827958,"end":141012344,"strand":1,"description":"protocadherin alpha 6 [Source:HGNC Symbol;Acc:HGNC:8672]"}, {"versioned_ensembl_gene_id":"ENSG00000070423.17","gene_symbol":"RNF126","gene_name":"ring finger protein 126 [Source:HGNC Symbol;Acc:HGNC:21151]","synonyms":"FLJ20552","biotype":"protein_coding","ncbi_id":"55658","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008]","start":647526,"end":663277,"strand":-1,"description":"ring finger protein 126 [Source:HGNC Symbol;Acc:HGNC:21151]"}, {"versioned_ensembl_gene_id":"ENSG00000278915.1","gene_symbol":"AC005609.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140875346,"end":140875922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271239.1","gene_symbol":"AC007423.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70778604,"end":70779230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267365.1","gene_symbol":"KCNJ2-AS1","gene_name":"KCNJ2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43720]","synonyms":"FLJ36644","biotype":"antisense_RNA","ncbi_id":"400617","summary":null,"start":70166961,"end":70169402,"strand":-1,"description":"KCNJ2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43720]"}, {"versioned_ensembl_gene_id":"ENSG00000140600.16","gene_symbol":"SH3GL3","gene_name":"SH3 domain containing GRB2 like 3, endophilin A3 [Source:HGNC Symbol;Acc:HGNC:10832]","synonyms":"CNSA3,SH3P13,SH3D2C,HsT19371,EEN-B2","biotype":"protein_coding","ncbi_id":"6457","summary":null,"start":83447228,"end":83618743,"strand":1,"description":"SH3 domain containing GRB2 like 3, endophilin A3 [Source:HGNC Symbol;Acc:HGNC:10832]"}, {"versioned_ensembl_gene_id":"ENSG00000279842.1","gene_symbol":"AC007603.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49900019,"end":49900524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235651.1","gene_symbol":"AC064850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135510546,"end":135511943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106952.7","gene_symbol":"TNFSF8","gene_name":"TNF superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:11938]","synonyms":"CD30LG,CD153","biotype":"protein_coding","ncbi_id":"944","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for TNFRSF8/CD30, which is a cell surface antigen and a marker for Hodgkin lymphoma and related hematologic malignancies. The engagement of this cytokine expressed on B cell surface plays an inhibitory role in modulating Ig class switch. This cytokine was shown to enhance cell proliferation of some lymphoma cell lines, while to induce cell death and reduce cell proliferation of other lymphoma cell lines. The pleiotropic biologic activities of this cytokine on different CD30+ lymphoma cell lines may play a pathophysiologic role in Hodgkin's and some non-Hodgkin's lymphomas. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":114893343,"end":114930595,"strand":-1,"description":"TNF superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:11938]"}, {"versioned_ensembl_gene_id":"ENSG00000224678.3","gene_symbol":"GAPDHP46","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:37804]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240711","summary":null,"start":92114803,"end":92115796,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:37804]"}, {"versioned_ensembl_gene_id":"ENSG00000266111.2","gene_symbol":"AC068025.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29352069,"end":29404105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173163.10","gene_symbol":"COMMD1","gene_name":"copper metabolism domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23024]","synonyms":"MURR1,MGC27155,C2orf5","biotype":"protein_coding","ncbi_id":"150684","summary":"COMMD1 is a regulator of copper homeostasis, sodium uptake, and NF-kappa-B (see MIM 164011) signaling (de Bie et al., 2005 [PubMed 16267171]).[supplied by OMIM, Sep 2009]","start":61888724,"end":62147247,"strand":1,"description":"copper metabolism domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23024]"}, {"versioned_ensembl_gene_id":"ENSG00000228034.1","gene_symbol":"HMGN2P21","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39386]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874467","summary":null,"start":70803157,"end":70803426,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39386]"}, {"versioned_ensembl_gene_id":"ENSG00000120075.5","gene_symbol":"HOXB5","gene_name":"homeobox B5 [Source:HGNC Symbol;Acc:HGNC:5116]","synonyms":"HOX2A,HOX2","biotype":"protein_coding","ncbi_id":"3215","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in lung and gut development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML) and the occurrence of bronchopulmonary sequestration (BPS) and congenital cystic adenomatoid malformation (CCAM) tissue. [provided by RefSeq, Jul 2008]","start":48591257,"end":48593961,"strand":-1,"description":"homeobox B5 [Source:HGNC Symbol;Acc:HGNC:5116]"}, {"versioned_ensembl_gene_id":"ENSG00000268529.1","gene_symbol":"CYP2T3P","gene_name":"cytochrome P450 family 2 subfamily T member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:18853]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"163007","summary":null,"start":41134722,"end":41137308,"strand":1,"description":"cytochrome P450 family 2 subfamily T member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:18853]"}, {"versioned_ensembl_gene_id":"ENSG00000251374.1","gene_symbol":"AC010598.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82265157,"end":82265259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280003.1","gene_symbol":"AC097637.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52217016,"end":52219012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183733.6","gene_symbol":"FIGLA","gene_name":"folliculogenesis specific bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:24669]","synonyms":"bHLHc8","biotype":"protein_coding","ncbi_id":"344018","summary":"This gene encodes a protein that functions in postnatal oocyte-specific gene expression. The protein is a basic helix-loop-helix transcription factor that regulates multiple oocyte-specific genes, including genes involved in folliculogenesis and those that encode the zona pellucida. Mutations in this gene cause premature ovarian failure type 6. [provided by RefSeq, Sep 2009]","start":70777310,"end":70790643,"strand":-1,"description":"folliculogenesis specific bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:24669]"}, {"versioned_ensembl_gene_id":"ENSG00000260011.2","gene_symbol":"AC132938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82381110,"end":82382690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263787.1","gene_symbol":"SKAP1-AS1","gene_name":"SKAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53166]","synonyms":"RP11-456D7.1","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48185938,"end":48204529,"strand":1,"description":"SKAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53166]"}, {"versioned_ensembl_gene_id":"ENSG00000271259.1","gene_symbol":"AC010201.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89371820,"end":89372359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235300.4","gene_symbol":"THRA1/BTR","gene_name":"uncharacterized LOC105371807 [Source:NCBI gene;Acc:105371807]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105371807","summary":null,"start":48294335,"end":48308762,"strand":1,"description":"uncharacterized LOC105371807 [Source:NCBI gene;Acc:105371807]"}, {"versioned_ensembl_gene_id":"ENSG00000136950.13","gene_symbol":"ARPC5L","gene_name":"actin related protein 2/3 complex subunit 5 like [Source:HGNC Symbol;Acc:HGNC:23366]","synonyms":"ARC16-2,MGC3038","biotype":"protein_coding","ncbi_id":"81873","summary":null,"start":124862130,"end":124877733,"strand":1,"description":"actin related protein 2/3 complex subunit 5 like [Source:HGNC Symbol;Acc:HGNC:23366]"}, {"versioned_ensembl_gene_id":"ENSG00000268225.2","gene_symbol":"AC010487.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52861807,"end":52864151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260898.5","gene_symbol":"ADPGK-AS1","gene_name":"ADPGK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44144]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287559","summary":null,"start":72782835,"end":72798199,"strand":1,"description":"ADPGK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44144]"}, {"versioned_ensembl_gene_id":"ENSG00000108950.11","gene_symbol":"FAM20A","gene_name":"FAM20A, golgi associated secretory pathway pseudokinase [Source:HGNC Symbol;Acc:HGNC:23015]","synonyms":"DKFZp434F2322","biotype":"protein_coding","ncbi_id":"54757","summary":"This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]","start":68535113,"end":68601389,"strand":-1,"description":"FAM20A, golgi associated secretory pathway pseudokinase [Source:HGNC Symbol;Acc:HGNC:23015]"}, {"versioned_ensembl_gene_id":"ENSG00000108932.11","gene_symbol":"SLC16A6","gene_name":"solute carrier family 16 member 6 [Source:HGNC Symbol;Acc:HGNC:10927]","synonyms":"MCT7,MCT6","biotype":"protein_coding","ncbi_id":"9120","summary":null,"start":68267026,"end":68291267,"strand":-1,"description":"solute carrier family 16 member 6 [Source:HGNC Symbol;Acc:HGNC:10927]"}, {"versioned_ensembl_gene_id":"ENSG00000283088.1","gene_symbol":"AC010487.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":52880663,"end":52962768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176715.15","gene_symbol":"ACSF3","gene_name":"acyl-CoA synthetase family member 3 [Source:HGNC Symbol;Acc:HGNC:27288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"197322","summary":"This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]","start":89088375,"end":89155846,"strand":1,"description":"acyl-CoA synthetase family member 3 [Source:HGNC Symbol;Acc:HGNC:27288]"}, {"versioned_ensembl_gene_id":"ENSG00000173762.7","gene_symbol":"CD7","gene_name":"CD7 molecule [Source:HGNC Symbol;Acc:HGNC:1695]","synonyms":"TP41,Tp40,LEU-9,GP40","biotype":"protein_coding","ncbi_id":"924","summary":"This gene encodes a transmembrane protein which is a member of the immunoglobulin superfamily. This protein is found on thymocytes and mature T cells. It plays an essential role in T-cell interactions and also in T-cell/B-cell interaction during early lymphoid development. [provided by RefSeq, Jul 2008]","start":82314868,"end":82317602,"strand":-1,"description":"CD7 molecule [Source:HGNC Symbol;Acc:HGNC:1695]"}, {"versioned_ensembl_gene_id":"ENSG00000260563.3","gene_symbol":"AC132872.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82293716,"end":82294910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227096.1","gene_symbol":"HMGB3P8","gene_name":"high mobility group box 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506039","summary":null,"start":116439468,"end":116440044,"strand":-1,"description":"high mobility group box 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39300]"}, {"versioned_ensembl_gene_id":"ENSG00000244551.2","gene_symbol":"RPL34P29","gene_name":"ribosomal protein L34 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271503","summary":null,"start":49935028,"end":49935352,"strand":1,"description":"ribosomal protein L34 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35631]"}, {"versioned_ensembl_gene_id":"ENSG00000113456.18","gene_symbol":"RAD1","gene_name":"RAD1 checkpoint DNA exonuclease [Source:HGNC Symbol;Acc:HGNC:9806]","synonyms":"REC1,HRAD1","biotype":"protein_coding","ncbi_id":"5810","summary":"This gene encodes a component of a heterotrimeric cell cycle checkpoint complex, known as the 9-1-1 complex, that is activated to stop cell cycle progression in response to DNA damage or incomplete DNA replication. The 9-1-1 complex is recruited by RAD17 to affected sites where it may attract specialized DNA polymerases and other DNA repair effectors. Alternatively spliced transcript variants of this gene have been described. [provided by RefSeq, Jan 2009]","start":34905264,"end":34918989,"strand":-1,"description":"RAD1 checkpoint DNA exonuclease [Source:HGNC Symbol;Acc:HGNC:9806]"}, {"versioned_ensembl_gene_id":"ENSG00000147378.11","gene_symbol":"FATE1","gene_name":"fetal and adult testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24683]","synonyms":"FATE,CT43","biotype":"protein_coding","ncbi_id":"89885","summary":"This gene encodes a cancer-testis antigen that is highly expressed in hepatocellular carcinomas and other tumors and weakly expressed in normal tissues except testis. The protein is strongly expressed in spermatogonia, primary spermatocytes, and Sertoli cells in seminiferous tubules. This protein may have a role in the control of early testicular differentiation and cell proliferation. [provided by RefSeq, Jan 2010]","start":151716035,"end":151723194,"strand":1,"description":"fetal and adult testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24683]"}, {"versioned_ensembl_gene_id":"ENSG00000168393.12","gene_symbol":"DTYMK","gene_name":"deoxythymidylate kinase [Source:HGNC Symbol;Acc:HGNC:3061]","synonyms":"TYMK,TMPK,CDC8","biotype":"protein_coding","ncbi_id":"1841","summary":null,"start":241675742,"end":241686991,"strand":-1,"description":"deoxythymidylate kinase [Source:HGNC Symbol;Acc:HGNC:3061]"}, {"versioned_ensembl_gene_id":"ENSG00000260565.6","gene_symbol":"ERVK13-1","gene_name":"endogenous retrovirus group K13 member 1 [Source:HGNC Symbol;Acc:HGNC:27548]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507321","summary":null,"start":2660349,"end":2673444,"strand":-1,"description":"endogenous retrovirus group K13 member 1 [Source:HGNC Symbol;Acc:HGNC:27548]"}, {"versioned_ensembl_gene_id":"ENSG00000131097.6","gene_symbol":"HIGD1B","gene_name":"HIG1 hypoxia inducible domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24318]","synonyms":"CLST11240-15,CLST11240","biotype":"protein_coding","ncbi_id":"51751","summary":"This gene encodes a member of the hypoxia inducible gene 1 (HIG1) domain family. The encoded protein is localized to the cell membrane and has been linked to tumorigenesis and the progression of pituitary adenomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":44846353,"end":44850480,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24318]"}, {"versioned_ensembl_gene_id":"ENSG00000260747.1","gene_symbol":"AC022968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68277802,"end":68278243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265863.1","gene_symbol":"AC007923.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31759795,"end":31761385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228768.3","gene_symbol":"AC003101.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31571142,"end":31575659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176177.9","gene_symbol":"ENTHD1","gene_name":"ENTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26352]","synonyms":"FLJ25421","biotype":"protein_coding","ncbi_id":"150350","summary":null,"start":39743044,"end":39893864,"strand":-1,"description":"ENTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26352]"}, {"versioned_ensembl_gene_id":"ENSG00000176256.10","gene_symbol":"HMGB4","gene_name":"high mobility group box 4 [Source:HGNC Symbol;Acc:HGNC:24954]","synonyms":"FLJ40388","biotype":"protein_coding","ncbi_id":"127540","summary":null,"start":33860475,"end":33864791,"strand":1,"description":"high mobility group box 4 [Source:HGNC Symbol;Acc:HGNC:24954]"}, {"versioned_ensembl_gene_id":"ENSG00000131435.12","gene_symbol":"PDLIM4","gene_name":"PDZ and LIM domain 4 [Source:HGNC Symbol;Acc:HGNC:16501]","synonyms":"RIL","biotype":"protein_coding","ncbi_id":"8572","summary":"This gene encodes a protein which may be involved in bone development. Mutations in this gene are associated with susceptibility to osteoporosis. [provided by RefSeq, Nov 2009]","start":132257671,"end":132273454,"strand":1,"description":"PDZ and LIM domain 4 [Source:HGNC Symbol;Acc:HGNC:16501]"}, {"versioned_ensembl_gene_id":"ENSG00000264151.5","gene_symbol":"AC090403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27336379,"end":27595164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277110.3","gene_symbol":"TRBV6-5","gene_name":"T-cell receptor beta variable 6-5 [Source:HGNC Symbol;Acc:HGNC:12230]","synonyms":"TRBV65,TCRBV6S5,TCRBV13S1","biotype":"TR_V_gene","ncbi_id":"28602","summary":null,"start":142472647,"end":142473148,"strand":1,"description":"T-cell receptor beta variable 6-5 [Source:HGNC Symbol;Acc:HGNC:12230]"}, {"versioned_ensembl_gene_id":"ENSG00000263405.1","gene_symbol":"AC068408.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27452514,"end":27453657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261645.5","gene_symbol":"DISC1FP1","gene_name":"DISC1 fusion partner 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33625]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101929222","summary":null,"start":90251232,"end":90915052,"strand":1,"description":"DISC1 fusion partner 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33625]"}, {"versioned_ensembl_gene_id":"ENSG00000214391.3","gene_symbol":"TUBAP2","gene_name":"tubulin alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399942","summary":null,"start":90282560,"end":90284172,"strand":1,"description":"tubulin alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14531]"}, {"versioned_ensembl_gene_id":"ENSG00000145040.3","gene_symbol":"UCN2","gene_name":"urocortin 2 [Source:HGNC Symbol;Acc:HGNC:18414]","synonyms":"URP,UCNI,UCN-II,SRP","biotype":"protein_coding","ncbi_id":"90226","summary":"This gene is a member of the sauvagine/corticotropin-releasing factor/urotensin I family. It is structurally related to the corticotropin-releasing factor (CRF) gene and the encoded product is an endogenous ligand for CRF type 2 receptors. In the brain it may be responsible for the effects of stress on appetite. In spite of the gene family name similarity, the product of this gene has no sequence similarity to urotensin II. [provided by RefSeq, Jul 2008]","start":48561727,"end":48563773,"strand":-1,"description":"urocortin 2 [Source:HGNC Symbol;Acc:HGNC:18414]"}, {"versioned_ensembl_gene_id":"ENSG00000277398.5","gene_symbol":"LILRA1","gene_name":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]","synonyms":"LIR6,LIR-6,CD85i","biotype":"protein_coding","ncbi_id":"11024","summary":"This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":54524093,"end":54532898,"strand":1,"description":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]"}, {"versioned_ensembl_gene_id":"ENSG00000283001.1","gene_symbol":"AL450426.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104520829,"end":104537180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169676.5","gene_symbol":"DRD5","gene_name":"dopamine receptor D5 [Source:HGNC Symbol;Acc:HGNC:3026]","synonyms":"DRD1L2,DRD1B","biotype":"protein_coding","ncbi_id":"1816","summary":"This gene encodes the D5 subtype of the dopamine receptor. The D5 subtype is a G-protein coupled receptor which stimulates adenylyl cyclase. This receptor is expressed in neurons in the limbic regions of the brain. It has a 10-fold higher affinity for dopamine than the D1 subtype. Pseudogenes related to this gene reside on chromosomes 1 and 2. [provided by RefSeq, Jul 2008]","start":9781680,"end":9784009,"strand":1,"description":"dopamine receptor D5 [Source:HGNC Symbol;Acc:HGNC:3026]"}, {"versioned_ensembl_gene_id":"ENSG00000266897.1","gene_symbol":"AC005546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13131571,"end":13132410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259003.1","gene_symbol":"AC243965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22556640,"end":22559037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213215.5","gene_symbol":"OR2F1","gene_name":"olfactory receptor family 2 subfamily F member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8246]","synonyms":"OR7-140,OR7-139,OR2F5,OR2F4,OR2F3P,OR2F3,OR14-60,OLF3","biotype":"polymorphic_pseudogene","ncbi_id":"26211","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":143954844,"end":143997312,"strand":1,"description":"olfactory receptor family 2 subfamily F member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8246]"}, {"versioned_ensembl_gene_id":"ENSG00000264257.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786355,"end":54790318,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000163116.9","gene_symbol":"STPG2","gene_name":"sperm tail PG-rich repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:28712]","synonyms":"MGC46496,C4orf37","biotype":"protein_coding","ncbi_id":"285555","summary":null,"start":97184093,"end":98143240,"strand":-1,"description":"sperm tail PG-rich repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:28712]"}, {"versioned_ensembl_gene_id":"ENSG00000223504.1","gene_symbol":"AL646090.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68055351,"end":68060502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060339.13","gene_symbol":"CCAR1","gene_name":"cell division cycle and apoptosis regulator 1 [Source:HGNC Symbol;Acc:HGNC:24236]","synonyms":"FLJ10590,CARP1,CARP-1","biotype":"protein_coding","ncbi_id":"55749","summary":null,"start":68721012,"end":68792377,"strand":1,"description":"cell division cycle and apoptosis regulator 1 [Source:HGNC Symbol;Acc:HGNC:24236]"}, {"versioned_ensembl_gene_id":"ENSG00000279384.1","gene_symbol":"AC080188.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":168843988,"end":168844735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164086.9","gene_symbol":"DUSP7","gene_name":"dual specificity phosphatase 7 [Source:HGNC Symbol;Acc:HGNC:3073]","synonyms":"PYST2,MKP-X","biotype":"protein_coding","ncbi_id":"1849","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. DUSP7 belongs to a class of DUSPs, designated MKPs, that dephosphorylate MAPK (mitogen-activated protein kinase) proteins ERK (see MIM 601795), JNK (see MIM 601158), and p38 (see MIM 600289) with specificity distinct from that of individual MKP proteins. MKPs contain a highly conserved C-terminal catalytic domain and an N-terminal Cdc25 (see MIM 116947)-like (CH2) domain. MAPK activation cascades mediate various physiologic processes, including cellular proliferation, apoptosis, differentiation, and stress responses (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":52048919,"end":52056550,"strand":-1,"description":"dual specificity phosphatase 7 [Source:HGNC Symbol;Acc:HGNC:3073]"}, {"versioned_ensembl_gene_id":"ENSG00000120910.14","gene_symbol":"PPP3CC","gene_name":"protein phosphatase 3 catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9316]","synonyms":"PP2Bgamma,CALNA3","biotype":"protein_coding","ncbi_id":"5533","summary":"Calcineurin is a calcium-dependent, calmodulin-stimulated protein phosphatase involved in the downstream regulation of dopaminergic signal transduction. Calcineurin is composed of a regulatory subunit and a catalytic subunit. The protein encoded by this gene represents one of the regulatory subunits that has been found for calcineurin. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":22440819,"end":22541142,"strand":1,"description":"protein phosphatase 3 catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9316]"}, {"versioned_ensembl_gene_id":"ENSG00000255439.6","gene_symbol":"AC135050.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31083439,"end":31094956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272865.1","gene_symbol":"AL591686.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":242147514,"end":242209129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255467.1","gene_symbol":"AP002433.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108105074,"end":108121684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279475.1","gene_symbol":"AC087894.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127825938,"end":127826286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256922.1","gene_symbol":"AC087894.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127793527,"end":127821183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242936.1","gene_symbol":"RPL30P6","gene_name":"ribosomal protein L30 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37015]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270980","summary":null,"start":95644952,"end":95645293,"strand":-1,"description":"ribosomal protein L30 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37015]"}, {"versioned_ensembl_gene_id":"ENSG00000255945.1","gene_symbol":"AC025252.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127598168,"end":127599715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258666.1","gene_symbol":"AL157871.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100333790,"end":100354061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000051825.14","gene_symbol":"MPHOSPH9","gene_name":"M-phase phosphoprotein 9 [Source:HGNC Symbol;Acc:HGNC:7215]","synonyms":"MPP9","biotype":"protein_coding","ncbi_id":"10198","summary":null,"start":123152320,"end":123244014,"strand":-1,"description":"M-phase phosphoprotein 9 [Source:HGNC Symbol;Acc:HGNC:7215]"}, {"versioned_ensembl_gene_id":"ENSG00000232650.5","gene_symbol":"LINC01780","gene_name":"long intergenic non-protein coding RNA 1780 [Source:HGNC Symbol;Acc:HGNC:52570]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378934","summary":null,"start":119328176,"end":119356182,"strand":1,"description":"long intergenic non-protein coding RNA 1780 [Source:HGNC Symbol;Acc:HGNC:52570]"}, {"versioned_ensembl_gene_id":"ENSG00000241818.1","gene_symbol":"AC123768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32656084,"end":32673065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164296.6","gene_symbol":"TIGD6","gene_name":"tigger transposable element derived 6 [Source:HGNC Symbol;Acc:HGNC:18332]","synonyms":"DKFZp761E2110","biotype":"protein_coding","ncbi_id":"81789","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. [provided by RefSeq, Oct 2009]","start":149993118,"end":150001167,"strand":-1,"description":"tigger transposable element derived 6 [Source:HGNC Symbol;Acc:HGNC:18332]"}, {"versioned_ensembl_gene_id":"ENSG00000263709.1","gene_symbol":"AC024619.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29140483,"end":29155489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248359.1","gene_symbol":"AC010280.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68531690,"end":68533530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258571.1","gene_symbol":"PTTG4P","gene_name":"pituitary tumor-transforming 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:20055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326315","summary":null,"start":71085482,"end":71085833,"strand":-1,"description":"pituitary tumor-transforming 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:20055]"}, {"versioned_ensembl_gene_id":"ENSG00000251361.1","gene_symbol":"AC012625.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93019663,"end":93068669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255276.1","gene_symbol":"RRM1-AS1","gene_name":"RRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40512]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478966","summary":null,"start":4137116,"end":4138257,"strand":-1,"description":"RRM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40512]"}, {"versioned_ensembl_gene_id":"ENSG00000236173.1","gene_symbol":"AL049612.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169809318,"end":169810102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218143.2","gene_symbol":"ERHP2","gene_name":"ERH pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41917]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874403","summary":null,"start":54016479,"end":54016777,"strand":-1,"description":"ERH pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41917]"}, {"versioned_ensembl_gene_id":"ENSG00000230169.1","gene_symbol":"RPL30P16","gene_name":"ribosomal protein L30 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:48340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289099","summary":null,"start":112538889,"end":112539317,"strand":1,"description":"ribosomal protein L30 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:48340]"}, {"versioned_ensembl_gene_id":"ENSG00000076513.16","gene_symbol":"ANKRD13A","gene_name":"ankyrin repeat domain 13A [Source:HGNC Symbol;Acc:HGNC:21268]","synonyms":"NY-REN-25,ANKRD13","biotype":"protein_coding","ncbi_id":"88455","summary":null,"start":109999186,"end":110039763,"strand":1,"description":"ankyrin repeat domain 13A [Source:HGNC Symbol;Acc:HGNC:21268]"}, {"versioned_ensembl_gene_id":"ENSG00000167548.14","gene_symbol":"KMT2D","gene_name":"lysine methyltransferase 2D [Source:HGNC Symbol;Acc:HGNC:7133]","synonyms":"TNRC21,MLL4,MLL2,CAGL114,ALR","biotype":"protein_coding","ncbi_id":"8085","summary":"The protein encoded by this gene is a histone methyltransferase that methylates the Lys-4 position of histone H3. The encoded protein is part of a large protein complex called ASCOM, which has been shown to be a transcriptional regulator of the beta-globin and estrogen receptor genes. Mutations in this gene have been shown to be a cause of Kabuki syndrome. [provided by RefSeq, Oct 2010]","start":49018975,"end":49059774,"strand":-1,"description":"lysine methyltransferase 2D [Source:HGNC Symbol;Acc:HGNC:7133]"}, {"versioned_ensembl_gene_id":"ENSG00000261166.1","gene_symbol":"AC073429.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136097797,"end":136099240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266967.6","gene_symbol":"AARSD1","gene_name":"alanyl-tRNA synthetase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28417]","synonyms":"MGC2744","biotype":"protein_coding","ncbi_id":"80755","summary":null,"start":42950526,"end":42964498,"strand":-1,"description":"alanyl-tRNA synthetase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28417]"}, {"versioned_ensembl_gene_id":"ENSG00000169635.9","gene_symbol":"HIC2","gene_name":"HIC ZBTB transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:18595]","synonyms":"ZNF907,ZBTB30,KIAA1020,HRG22","biotype":"protein_coding","ncbi_id":"23119","summary":null,"start":21417404,"end":21451463,"strand":1,"description":"HIC ZBTB transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:18595]"}, {"versioned_ensembl_gene_id":"ENSG00000156639.11","gene_symbol":"ZFAND3","gene_name":"zinc finger AN1-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18019]","synonyms":"TEX27,FLJ13222","biotype":"protein_coding","ncbi_id":"60685","summary":null,"start":37819499,"end":38154624,"strand":1,"description":"zinc finger AN1-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18019]"}, {"versioned_ensembl_gene_id":"ENSG00000282464.1","gene_symbol":"AC137894.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":528907,"end":532261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272916.5","gene_symbol":"AC022400.6","gene_name":"bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 2 isoform 2 [Source:RefSeq peptide;Acc:NP_001317036]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":73796514,"end":73811651,"strand":-1,"description":"bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 2 isoform 2 [Source:RefSeq peptide;Acc:NP_001317036]"}, {"versioned_ensembl_gene_id":"ENSG00000248330.5","gene_symbol":"LINC00613","gene_name":"long intergenic non-protein coding RNA 613 [Source:HGNC Symbol;Acc:HGNC:44060]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507528","summary":null,"start":135866983,"end":135913680,"strand":-1,"description":"long intergenic non-protein coding RNA 613 [Source:HGNC Symbol;Acc:HGNC:44060]"}, {"versioned_ensembl_gene_id":"ENSG00000250865.1","gene_symbol":"AC105362.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135792384,"end":135805904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258496.1","gene_symbol":"AL352955.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87251103,"end":87251679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124019.9","gene_symbol":"FAM124B","gene_name":"family with sequence similarity 124 member B [Source:HGNC Symbol;Acc:HGNC:26224]","synonyms":"FLJ22746","biotype":"protein_coding","ncbi_id":"79843","summary":null,"start":224378698,"end":224402085,"strand":-1,"description":"family with sequence similarity 124 member B [Source:HGNC Symbol;Acc:HGNC:26224]"}, {"versioned_ensembl_gene_id":"ENSG00000211847.1","gene_symbol":"TRAJ42","gene_name":"T-cell receptor alpha joining 42 [Source:HGNC Symbol;Acc:HGNC:12073]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28713","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22496887,"end":22496952,"strand":1,"description":"T-cell receptor alpha joining 42 [Source:HGNC Symbol;Acc:HGNC:12073]"}, {"versioned_ensembl_gene_id":"ENSG00000258828.2","gene_symbol":"KRT8P2","gene_name":"keratin 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20282]","synonyms":"OTTHUMG00000135122","biotype":"processed_pseudogene","ncbi_id":"390472","summary":null,"start":43540883,"end":43541826,"strand":-1,"description":"keratin 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20282]"}, {"versioned_ensembl_gene_id":"ENSG00000255128.1","gene_symbol":"AC130360.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7418991,"end":7420546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238099.2","gene_symbol":"LINC01625","gene_name":"long intergenic non-protein coding RNA 1625 [Source:HGNC Symbol;Acc:HGNC:52052]","synonyms":"TCONS_00011139","biotype":"lincRNA","ncbi_id":"645434","summary":null,"start":139468995,"end":139474596,"strand":-1,"description":"long intergenic non-protein coding RNA 1625 [Source:HGNC Symbol;Acc:HGNC:52052]"}, {"versioned_ensembl_gene_id":"ENSG00000228247.1","gene_symbol":"UBBP2","gene_name":"ubiquitin B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12465]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"23668","summary":null,"start":217850403,"end":217850633,"strand":-1,"description":"ubiquitin B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12465]"}, {"versioned_ensembl_gene_id":"ENSG00000130962.17","gene_symbol":"PRRG1","gene_name":"proline rich and Gla domain 1 [Source:HGNC Symbol;Acc:HGNC:9469]","synonyms":"PRGP1","biotype":"protein_coding","ncbi_id":"5638","summary":"This gene encodes a vitamin K-dependent, gamma-carboxyglutamic acid (Gla)-containing, single-pass transmembrane protein. This protein contains a Gla domain at the N-terminus, preceded by a propeptide sequence required for post-translational gamma-carboxylation of specific glutamic acid residues by a vitamin K-dependent gamma-carboxylase. The C-terminus is proline-rich containing PPXY and PXXP motifs found in a variety of signaling and cytoskeletal proteins. This gene is highly expressed in the spinal cord. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]","start":37349275,"end":37457295,"strand":1,"description":"proline rich and Gla domain 1 [Source:HGNC Symbol;Acc:HGNC:9469]"}, {"versioned_ensembl_gene_id":"ENSG00000104321.10","gene_symbol":"TRPA1","gene_name":"transient receptor potential cation channel subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:497]","synonyms":"ANKTM1","biotype":"protein_coding","ncbi_id":"8989","summary":"The structure of the protein encoded by this gene is highly related to both the protein ankyrin and transmembrane proteins. The specific function of this protein has not yet been determined; however, studies indicate the function may involve a role in signal transduction and growth control. [provided by RefSeq, Jul 2008]","start":72019917,"end":72075617,"strand":-1,"description":"transient receptor potential cation channel subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:497]"}, {"versioned_ensembl_gene_id":"ENSG00000130176.7","gene_symbol":"CNN1","gene_name":"calponin 1 [Source:HGNC Symbol;Acc:HGNC:2155]","synonyms":"SMCC,Sm-Calp","biotype":"protein_coding","ncbi_id":"1264","summary":null,"start":11538717,"end":11550323,"strand":1,"description":"calponin 1 [Source:HGNC Symbol;Acc:HGNC:2155]"}, {"versioned_ensembl_gene_id":"ENSG00000240652.1","gene_symbol":"AP001024.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107908420,"end":107908764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007314.12","gene_symbol":"SCN4A","gene_name":"sodium voltage-gated channel alpha subunit 4 [Source:HGNC Symbol;Acc:HGNC:10591]","synonyms":"SkM1,Nav1.4,HYPP,HYKPP","biotype":"protein_coding","ncbi_id":"6329","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. It is expressed in skeletal muscle, and mutations in this gene have been linked to several myotonia and periodic paralysis disorders. [provided by RefSeq, Jul 2008]","start":63938554,"end":63972918,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 4 [Source:HGNC Symbol;Acc:HGNC:10591]"}, {"versioned_ensembl_gene_id":"ENSG00000137491.14","gene_symbol":"SLCO2B1","gene_name":"solute carrier organic anion transporter family member 2B1 [Source:HGNC Symbol;Acc:HGNC:10962]","synonyms":"SLC21A9,OATP2B1,OATP-B","biotype":"protein_coding","ncbi_id":"11309","summary":"This locus encodes a member of the organic anion-transporting polypeptide family of membrane proteins. The protein encoded by this locus may function in regulation of placental uptake of sulfated steroids. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]","start":75100563,"end":75206549,"strand":1,"description":"solute carrier organic anion transporter family member 2B1 [Source:HGNC Symbol;Acc:HGNC:10962]"}, {"versioned_ensembl_gene_id":"ENSG00000144410.4","gene_symbol":"CPO","gene_name":"carboxypeptidase O [Source:HGNC Symbol;Acc:HGNC:21011]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130749","summary":"This gene is a member of the metallocarboxypeptidase gene family. [provided by RefSeq, Jan 2011]","start":206939554,"end":206969474,"strand":1,"description":"carboxypeptidase O [Source:HGNC Symbol;Acc:HGNC:21011]"}, {"versioned_ensembl_gene_id":"ENSG00000175164.13","gene_symbol":"ABO","gene_name":"ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase [Source:HGNC Symbol;Acc:HGNC:79]","synonyms":"A3GALT1,A3GALNT","biotype":"protein_coding","ncbi_id":"28","summary":"This gene encodes proteins related to the first discovered blood group system, ABO. Variation in the ABO gene (chromosome 9q34.2) is the basis of the ABO blood group, thus the presence of an allele determines the blood group in an individual. The 'O' blood group is caused by a deletion of guanine-258 near the N-terminus of the protein which results in a frameshift and translation of an almost entirely different protein. Individuals with the A, B, and AB alleles express glycosyltransferase activities that convert the H antigen into the A or B antigen. Other minor alleles have been found for this gene. This locus has been identified as a susceptibility locus for severe coronavirus disease 2019 (COVID-19) by genome-wide association study. [provided by RefSeq, Aug 2020]","start":133250401,"end":133275214,"strand":-1,"description":"ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase [Source:HGNC Symbol;Acc:HGNC:79]"}, {"versioned_ensembl_gene_id":"ENSG00000176920.11","gene_symbol":"FUT2","gene_name":"fucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4013]","synonyms":"sej,SEC2,Se2,SE","biotype":"protein_coding","ncbi_id":"2524","summary":"The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of a precursor of the H antigen, which is required for the final step in the soluble A and B antigen synthesis pathway. This gene is one of two encoding the galactoside 2-L-fucosyltransferase enzyme. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":48695971,"end":48705950,"strand":1,"description":"fucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4013]"}, {"versioned_ensembl_gene_id":"ENSG00000253379.5","gene_symbol":"AC099805.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71403440,"end":71592025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249919.1","gene_symbol":"FABP5P6","gene_name":"fatty acid binding protein 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31069]","synonyms":"FABP5L6","biotype":"processed_pseudogene","ncbi_id":"100130687","summary":null,"start":119555250,"end":119555658,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31069]"}, {"versioned_ensembl_gene_id":"ENSG00000158470.5","gene_symbol":"B4GALT5","gene_name":"beta-1,4-galactosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:928]","synonyms":"beta4GalT-V","biotype":"protein_coding","ncbi_id":"9334","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. The function of the enzyme encoded by this gene is not clear. This gene was previously designated as B4GALT4 but was renamed to B4GALT5. In the literature it is also referred to as beta4GalT2. [provided by RefSeq, Jul 2008]","start":49632945,"end":49713878,"strand":-1,"description":"beta-1,4-galactosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:928]"}, {"versioned_ensembl_gene_id":"ENSG00000237118.3","gene_symbol":"CYP2F2P","gene_name":"cytochrome P450 family 2 subfamily F member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:18851]","synonyms":"CYP2F1P","biotype":"transcribed_processed_pseudogene","ncbi_id":"171427","summary":null,"start":40818414,"end":40826772,"strand":-1,"description":"cytochrome P450 family 2 subfamily F member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:18851]"}, {"versioned_ensembl_gene_id":"ENSG00000179344.16","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"CELIAC1,IDDM1,HLA-DQB","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32659467,"end":32668383,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000269437.6","gene_symbol":"NXF2B","gene_name":"nuclear RNA export factor 2B [Source:HGNC Symbol;Acc:HGNC:23984]","synonyms":"bA353J17.1","biotype":"protein_coding","ncbi_id":"728343","summary":"This gene encodes a member of a family of nuclear RNA export proteins. The encoded protein is associated with the nuclear envelope and aids in the export of mRNAs. There is a closely related paralog of this gene located adjacent on chromosome X and on the opposite strand. [provided by RefSeq, Jun 2015]","start":102360395,"end":102463274,"strand":-1,"description":"nuclear RNA export factor 2B [Source:HGNC Symbol;Acc:HGNC:23984]"}, {"versioned_ensembl_gene_id":"ENSG00000206053.12","gene_symbol":"JPT2","gene_name":"Jupiter microtubule associated homolog 2 [Source:HGNC Symbol;Acc:HGNC:14137]","synonyms":"HN1L,FLJ13092,C16orf34,L11,KIAA1426","biotype":"protein_coding","ncbi_id":"90861","summary":null,"start":1678256,"end":1702280,"strand":1,"description":"Jupiter microtubule associated homolog 2 [Source:HGNC Symbol;Acc:HGNC:14137]"}, {"versioned_ensembl_gene_id":"ENSG00000254621.1","gene_symbol":"SETP16","gene_name":"SET pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649925","summary":null,"start":118833846,"end":118834556,"strand":-1,"description":"SET pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42935]"}, {"versioned_ensembl_gene_id":"ENSG00000119440.8","gene_symbol":"LCN1P1","gene_name":"lipocalin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23412]","synonyms":"LCN1L1,bA430N14.2","biotype":"unprocessed_pseudogene","ncbi_id":"286310","summary":null,"start":133224905,"end":133228591,"strand":-1,"description":"lipocalin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23412]"}, {"versioned_ensembl_gene_id":"ENSG00000173548.8","gene_symbol":"SNX33","gene_name":"sorting nexin 33 [Source:HGNC Symbol;Acc:HGNC:28468]","synonyms":"SNX30,SH3PXD3C,SH3PX3,MGC32065","biotype":"protein_coding","ncbi_id":"257364","summary":"The protein encoded by this gene is involved in cytoskeletal reorganization, vesicle trafficking, endocytosis, and mitosis. The encoded protein is essential for the creation of the cleavage furrow during mitosis and for completion of mitosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":75647906,"end":75662301,"strand":1,"description":"sorting nexin 33 [Source:HGNC Symbol;Acc:HGNC:28468]"}, {"versioned_ensembl_gene_id":"ENSG00000214563.2","gene_symbol":"GAPDHP15","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:13950]","synonyms":"GAPDP15,GAPDH-Lp,b55C20.4","biotype":"processed_pseudogene","ncbi_id":"642317","summary":null,"start":57967687,"end":57968661,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:13950]"}, {"versioned_ensembl_gene_id":"ENSG00000247810.6","gene_symbol":"AL136537.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37078577,"end":37125424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277885.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"cl-49,nkat5,183ActI,CD158J","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738243,"end":54752150,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000228802.1","gene_symbol":"AC073641.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":223965701,"end":223967706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254484.1","gene_symbol":"AP002336.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":70319928,"end":70321415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183668.17","gene_symbol":"PSG9","gene_name":"pregnancy specific beta-1-glycoprotein 9 [Source:HGNC Symbol;Acc:HGNC:9526]","synonyms":"PSGII,PSG11","biotype":"protein_coding","ncbi_id":"5678","summary":"The protein encoded by this gene is a member of the pregnancy-specific glycoprotein (PSG) family. This protein family and the closely related carcinoembryonic antigen cell adhesion molecule (CEACAM) gene family are both members of the immunoglobulin superfamily, and are organized as a large gene cluster. This protein is thought to inhibit platelet-fibrinogen interactions. Several studies suggest that reduced serum concentrations of PSGs are associated with fetal growth restrictions, while up-regulation of this gene has been observed in colorectal cancers. Several pseudogenes of this gene are found on chromosome 19. Alternative splicing results in multiple transcript variants that encode multiple protein isoforms. [provided by RefSeq, Sep 2014]","start":43211791,"end":43269530,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 9 [Source:HGNC Symbol;Acc:HGNC:9526]"}, {"versioned_ensembl_gene_id":"ENSG00000271680.1","gene_symbol":"AC098935.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206905928,"end":206906393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225811.1","gene_symbol":"AL354771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190264898,"end":190362270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197540.7","gene_symbol":"GZMM","gene_name":"granzyme M [Source:HGNC Symbol;Acc:HGNC:4712]","synonyms":"MET1,LMET1","biotype":"protein_coding","ncbi_id":"3004","summary":"Human natural killer (NK) cells and activated lymphocytes express and store a distinct subset of neutral serine proteases together with proteoglycans and other immune effector molecules in large cytoplasmic granules. These serine proteases are collectively termed granzymes and include 4 distinct gene products: granzyme A, granzyme B, granzyme H, and the protein encoded by this gene, granzyme M. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":544034,"end":549924,"strand":1,"description":"granzyme M [Source:HGNC Symbol;Acc:HGNC:4712]"}, {"versioned_ensembl_gene_id":"ENSG00000259101.1","gene_symbol":"CR936239.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31689075,"end":31700087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226945.1","gene_symbol":"AC098935.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206907619,"end":206908229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232150.3","gene_symbol":"ST13P4","gene_name":"ST13, Hsp70 interacting protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18487]","synonyms":"FAM10A4P,FAM10A4","biotype":"processed_pseudogene","ncbi_id":"145165","summary":null,"start":50172089,"end":50173181,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:18487]"}, {"versioned_ensembl_gene_id":"ENSG00000143995.19","gene_symbol":"MEIS1","gene_name":"Meis homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7000]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4211","summary":"Homeobox genes, of which the most well-characterized category is represented by the HOX genes, play a crucial role in normal development. In addition, several homeoproteins are involved in neoplasia. This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. [provided by RefSeq, Jul 2008]","start":66433452,"end":66573869,"strand":1,"description":"Meis homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7000]"}, {"versioned_ensembl_gene_id":"ENSG00000204250.3","gene_symbol":"LINC00587","gene_name":"long intergenic non-protein coding RNA 587 [Source:HGNC Symbol;Acc:HGNC:31372]","synonyms":"C9orf107,bA785H23.1","biotype":"lincRNA","ncbi_id":"414319","summary":null,"start":102519636,"end":102657514,"strand":1,"description":"long intergenic non-protein coding RNA 587 [Source:HGNC Symbol;Acc:HGNC:31372]"}, {"versioned_ensembl_gene_id":"ENSG00000112406.4","gene_symbol":"HECA","gene_name":"hdc homolog, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:21041]","synonyms":"hHDC,HDCL,HDC,dJ225E12.1","biotype":"protein_coding","ncbi_id":"51696","summary":"This gene encodes the homolog of the Drosophila headcase protein, a highly basic, cytoplasmic protein that regulates the re-entry of imaginal cells into the mitotic cycle during adult morphogenesis. In Drosophila, the encoded protein also inhibits terminal branching of neighboring cells during tracheal development. [provided by RefSeq, Jul 2008]","start":139135112,"end":139180802,"strand":1,"description":"hdc homolog, cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:21041]"}, {"versioned_ensembl_gene_id":"ENSG00000152266.6","gene_symbol":"PTH","gene_name":"parathyroid hormone [Source:HGNC Symbol;Acc:HGNC:9606]","synonyms":"PTH1","biotype":"protein_coding","ncbi_id":"5741","summary":"This gene encodes a member of the parathyroid family of proteins. The encoded preproprotein is proteolytically processed to generate a protein that binds to the parathyroid hormone/parathyroid hormone-related peptide receptor and regulates blood calcium and phosphate levels. Excess production of the encoded protein, known as hyperparathyroidism, can result in hypercalcemia and kidney stones. On the other hand, defective processing of the encoded protein may lead to hypoparathyroidism, which can result in hypocalcemia and numbness. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":13492055,"end":13496181,"strand":-1,"description":"parathyroid hormone [Source:HGNC Symbol;Acc:HGNC:9606]"}, {"versioned_ensembl_gene_id":"ENSG00000231329.7","gene_symbol":"AL031772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139144204,"end":139239653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230418.2","gene_symbol":"ARL2BPP7","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39451]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131629","summary":null,"start":102055252,"end":102055741,"strand":-1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39451]"}, {"versioned_ensembl_gene_id":"ENSG00000238054.1","gene_symbol":"AL691515.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188869477,"end":188887434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227885.1","gene_symbol":"AL590652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53740749,"end":53747022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236903.1","gene_symbol":"CR388202.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31865942,"end":31866235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235083.1","gene_symbol":"AL929288.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188671353,"end":188671759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230452.1","gene_symbol":"LINC01381","gene_name":"long intergenic non-protein coding RNA 1381 [Source:HGNC Symbol;Acc:HGNC:50653]","synonyms":"TCONS_00002860,DADOT","biotype":"antisense_RNA","ncbi_id":"106144568","summary":null,"start":25204313,"end":25209202,"strand":1,"description":"long intergenic non-protein coding RNA 1381 [Source:HGNC Symbol;Acc:HGNC:50653]"}, {"versioned_ensembl_gene_id":"ENSG00000253558.1","gene_symbol":"AC024568.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":78041879,"end":78044138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279874.1","gene_symbol":"AC064859.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123850522,"end":123850695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277106.2","gene_symbol":"SPPL2C","gene_name":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]","synonyms":"IMP5,IMP5","biotype":"protein_coding","ncbi_id":"162540","summary":null,"start":45856453,"end":45858690,"strand":1,"description":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]"}, {"versioned_ensembl_gene_id":"ENSG00000259068.1","gene_symbol":"TRAV37","gene_name":"T-cell receptor alpha variable 37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12136]","synonyms":null,"biotype":"TR_V_pseudogene","ncbi_id":"28645","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22265749,"end":22266264,"strand":1,"description":"T-cell receptor alpha variable 37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12136]"}, {"versioned_ensembl_gene_id":"ENSG00000261426.1","gene_symbol":"AC144833.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27362310,"end":27366398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234082.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31618650,"end":31619484,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000171227.6","gene_symbol":"TMEM37","gene_name":"transmembrane protein 37 [Source:HGNC Symbol;Acc:HGNC:18216]","synonyms":"PR1,PR","biotype":"protein_coding","ncbi_id":"140738","summary":null,"start":119429901,"end":119438520,"strand":1,"description":"transmembrane protein 37 [Source:HGNC Symbol;Acc:HGNC:18216]"}, {"versioned_ensembl_gene_id":"ENSG00000251360.2","gene_symbol":"KHDC1P1","gene_name":"KH homology domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43757]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653194","summary":null,"start":73209083,"end":73210080,"strand":-1,"description":"KH homology domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43757]"}, {"versioned_ensembl_gene_id":"ENSG00000233470.1","gene_symbol":"AL360175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50514035,"end":50521104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239626.1","gene_symbol":"RPSAP41","gene_name":"ribosomal protein SA pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36663]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270918","summary":null,"start":73290403,"end":73291262,"strand":1,"description":"ribosomal protein SA pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:36663]"}, {"versioned_ensembl_gene_id":"ENSG00000230900.5","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G2,NG38,ATP6G,Em:AC004181.3,Vma10","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31620808,"end":31623190,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000235899.1","gene_symbol":"LINC01564","gene_name":"long intergenic non-protein coding RNA 1564 [Source:HGNC Symbol;Acc:HGNC:51361]","synonyms":"TCONS_00011314","biotype":"antisense_RNA","ncbi_id":"101927171","summary":null,"start":53628380,"end":53631394,"strand":1,"description":"long intergenic non-protein coding RNA 1564 [Source:HGNC Symbol;Acc:HGNC:51361]"}, {"versioned_ensembl_gene_id":"ENSG00000282612.1","gene_symbol":"TAS2R20","gene_name":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]","synonyms":"TAS2R49,T2R56,T2R20","biotype":"protein_coding","ncbi_id":"259295","summary":"This gene encodes a member of the taste receptor two family of class C G-protein coupled receptors. Receptors of this family have a short extracellular N-terminus, seven transmembrane helices, three extracellular loops and three intracellular loops, and an intracellular C-terminus. Members of this family are expressed in a subset of taste receptor cells, where they function in bitter taste reception, as well as in non-gustatory cells including those of the brain, reproductive organs, respiratory system, and gastrointestinal system. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2016]","start":10996484,"end":10997864,"strand":-1,"description":"taste 2 receptor member 20 [Source:HGNC Symbol;Acc:HGNC:19109]"}, {"versioned_ensembl_gene_id":"ENSG00000262470.2","gene_symbol":"TVP23CP2","gene_name":"TVP23C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"261735","summary":null,"start":14200357,"end":14200979,"strand":1,"description":"TVP23C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44647]"}, {"versioned_ensembl_gene_id":"ENSG00000124762.13","gene_symbol":"CDKN1A","gene_name":"cyclin dependent kinase inhibitor 1A [Source:HGNC Symbol;Acc:HGNC:1784]","synonyms":"P21,CIP1,CDKN1,CAP20,WAF1,SDI1,p21Cip1/Waf1,p21CIP1","biotype":"protein_coding","ncbi_id":"1026","summary":"This gene encodes a potent cyclin-dependent kinase inhibitor. The encoded protein binds to and inhibits the activity of cyclin-cyclin-dependent kinase2 or -cyclin-dependent kinase4 complexes, and thus functions as a regulator of cell cycle progression at G1. The expression of this gene is tightly controlled by the tumor suppressor protein p53, through which this protein mediates the p53-dependent cell cycle G1 phase arrest in response to a variety of stress stimuli. This protein can interact with proliferating cell nuclear antigen, a DNA polymerase accessory factor, and plays a regulatory role in S phase DNA replication and DNA damage repair. This protein was reported to be specifically cleaved by CASP3-like caspases, which thus leads to a dramatic activation of cyclin-dependent kinase2, and may be instrumental in the execution of apoptosis following caspase activation. Mice that lack this gene have the ability to regenerate damaged or missing tissue. Multiple alternatively spliced variants have been found for this gene. [provided by RefSeq, Sep 2015]","start":36676460,"end":36687339,"strand":1,"description":"cyclin dependent kinase inhibitor 1A [Source:HGNC Symbol;Acc:HGNC:1784]"}, {"versioned_ensembl_gene_id":"ENSG00000229668.1","gene_symbol":"AL133384.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114501997,"end":114502347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240478.1","gene_symbol":"AC012081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182121884,"end":182142137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168040.4","gene_symbol":"FADD","gene_name":"Fas associated via death domain [Source:HGNC Symbol;Acc:HGNC:3573]","synonyms":"MORT1,GIG3","biotype":"protein_coding","ncbi_id":"8772","summary":"The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development. [provided by RefSeq, Jul 2008]","start":70203163,"end":70207390,"strand":1,"description":"Fas associated via death domain [Source:HGNC Symbol;Acc:HGNC:3573]"}, {"versioned_ensembl_gene_id":"ENSG00000253177.1","gene_symbol":"AC104211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92668836,"end":92679594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278736.1","gene_symbol":"FO393412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48701491,"end":48701872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168772.10","gene_symbol":"CXXC4","gene_name":"CXXC finger protein 4 [Source:HGNC Symbol;Acc:HGNC:24593]","synonyms":"IDAX","biotype":"protein_coding","ncbi_id":"80319","summary":"This gene encodes a CXXC-type zinc finger domain-containing protein that functions as an antagonist of the canonical wingless/integrated signaling pathway. The encoded protein negatively regulates wingless/integrated signaling through interaction with the post synaptic density protein/ Drosophila disc large tumor suppressor/ zonula occludens-1 protein domain of Dishevelled, a scaffolding protein required for the stabilization of the transcriptional co-activator beta-catenin. In addition, the CXXC domain of this protein has been shown to bind unmethylated CpG dinucleotides, localize to promoters and CpG islands, and interact with the catalytic domain of methylcytosine dioxygenase ten-eleven-translocation 2, an iron and alpha-ketoglutarate-dependent dioxygenase that modifies the methylation status of DNA. In humans, a mutation in this gene has been associated with development of malignant renal cell carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":104468312,"end":104494901,"strand":-1,"description":"CXXC finger protein 4 [Source:HGNC Symbol;Acc:HGNC:24593]"}, {"versioned_ensembl_gene_id":"ENSG00000169884.13","gene_symbol":"WNT10B","gene_name":"Wnt family member 10B [Source:HGNC Symbol;Acc:HGNC:12775]","synonyms":"WNT-12,SHFM6","biotype":"protein_coding","ncbi_id":"7480","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It may be involved in breast cancer, and its protein signaling is likely a molecular switch that governs adipogenesis. This protein is 96% identical to the mouse Wnt10b protein at the amino acid level. This gene is clustered with another family member, WNT1, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008]","start":48965340,"end":48971763,"strand":-1,"description":"Wnt family member 10B [Source:HGNC Symbol;Acc:HGNC:12775]"}, {"versioned_ensembl_gene_id":"ENSG00000274503.1","gene_symbol":"AC123912.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21592727,"end":21593041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268555.1","gene_symbol":"AC123912.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21570822,"end":21587322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204860.4","gene_symbol":"FAM201A","gene_name":"family with sequence similarity 201 member A [Source:HGNC Symbol;Acc:HGNC:27239]","synonyms":"C9orf122","biotype":"antisense_RNA","ncbi_id":"158228","summary":null,"start":38620474,"end":38624990,"strand":1,"description":"family with sequence similarity 201 member A [Source:HGNC Symbol;Acc:HGNC:27239]"}, {"versioned_ensembl_gene_id":"ENSG00000168491.9","gene_symbol":"CCDC110","gene_name":"coiled-coil domain containing 110 [Source:HGNC Symbol;Acc:HGNC:28504]","synonyms":"MGC33607,KM-HN-1,CT52","biotype":"protein_coding","ncbi_id":"256309","summary":null,"start":185445182,"end":185471759,"strand":-1,"description":"coiled-coil domain containing 110 [Source:HGNC Symbol;Acc:HGNC:28504]"}, {"versioned_ensembl_gene_id":"ENSG00000273325.1","gene_symbol":"AL008723.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32284683,"end":32285131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120696.8","gene_symbol":"KBTBD7","gene_name":"kelch repeat and BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:25266]","synonyms":"DKFZP434E2318","biotype":"protein_coding","ncbi_id":"84078","summary":"The protein encoded by this gene is a transcriptional activator, having been shown to increase the transcription of activator protein-1 and serum response element. The encoded protein can also form a complex with KBTBD6 and CUL3, which regulates the ubiquitylation and degradation of TIAM1, which is a regulator of RAC1. [provided by RefSeq, Jul 2016]","start":41189833,"end":41194566,"strand":-1,"description":"kelch repeat and BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:25266]"}, {"versioned_ensembl_gene_id":"ENSG00000270815.1","gene_symbol":"AC019159.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124778454,"end":124778640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219368.3","gene_symbol":"ZNF299P","gene_name":"zinc finger protein 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:13088]","synonyms":"ZNF299P1,ZNF299","biotype":"processed_pseudogene","ncbi_id":"54012","summary":null,"start":23090028,"end":23091831,"strand":-1,"description":"zinc finger protein 299, pseudogene [Source:HGNC Symbol;Acc:HGNC:13088]"}, {"versioned_ensembl_gene_id":"ENSG00000213277.3","gene_symbol":"MARCKSL1P1","gene_name":"MARCKS like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100913183","summary":null,"start":103175554,"end":103176094,"strand":1,"description":"MARCKS like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45239]"}, {"versioned_ensembl_gene_id":"ENSG00000236814.1","gene_symbol":"AC046176.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56050038,"end":56051207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173039.18","gene_symbol":"RELA","gene_name":"RELA proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9955]","synonyms":"p65,NFKB3","biotype":"protein_coding","ncbi_id":"5970","summary":"NF-kappa-B is a ubiquitous transcription factor involved in several biological processes. It is held in the cytoplasm in an inactive state by specific inhibitors. Upon degradation of the inhibitor, NF-kappa-B moves to the nucleus and activates transcription of specific genes. NF-kappa-B is composed of NFKB1 or NFKB2 bound to either REL, RELA, or RELB. The most abundant form of NF-kappa-B is NFKB1 complexed with the product of this gene, RELA. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":65653596,"end":65663094,"strand":-1,"description":"RELA proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9955]"}, {"versioned_ensembl_gene_id":"ENSG00000275121.1","gene_symbol":"AC211486.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75237293,"end":75237405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263081.1","gene_symbol":"AC211486.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75232928,"end":75233924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255501.1","gene_symbol":"CARD18","gene_name":"caspase recruitment domain family member 18 [Source:HGNC Symbol;Acc:HGNC:28861]","synonyms":"UNQ5804,pseudo-ICE,ICEBERG","biotype":"protein_coding","ncbi_id":"59082","summary":null,"start":105137721,"end":105139726,"strand":-1,"description":"caspase recruitment domain family member 18 [Source:HGNC Symbol;Acc:HGNC:28861]"}, {"versioned_ensembl_gene_id":"ENSG00000255430.1","gene_symbol":"CASP1P1","gene_name":"caspase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43775]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874457","summary":null,"start":105122661,"end":105123339,"strand":-1,"description":"caspase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43775]"}, {"versioned_ensembl_gene_id":"ENSG00000271882.1","gene_symbol":"AP001330.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101208148,"end":101208558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240445.3","gene_symbol":"FOXO3B","gene_name":"forkhead box O3B pseudogene [Source:HGNC Symbol;Acc:HGNC:3822]","synonyms":"FKHRL1P1","biotype":"processed_pseudogene","ncbi_id":"2310","summary":null,"start":18670946,"end":18672873,"strand":-1,"description":"forkhead box O3B pseudogene [Source:HGNC Symbol;Acc:HGNC:3822]"}, {"versioned_ensembl_gene_id":"ENSG00000140382.14","gene_symbol":"HMG20A","gene_name":"high mobility group 20A [Source:HGNC Symbol;Acc:HGNC:5001]","synonyms":"HMGXB1,HMGX1,FLJ10739","biotype":"protein_coding","ncbi_id":"10363","summary":null,"start":77420412,"end":77485607,"strand":1,"description":"high mobility group 20A [Source:HGNC Symbol;Acc:HGNC:5001]"}, {"versioned_ensembl_gene_id":"ENSG00000128045.6","gene_symbol":"RASL11B","gene_name":"RAS like family 11 member B [Source:HGNC Symbol;Acc:HGNC:23804]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65997","summary":"RASL11B is a member of the small GTPase protein family with a high degree of similarity to RAS (see HRAS, MIM 190020) proteins.[supplied by OMIM, Nov 2008]","start":52862290,"end":52866835,"strand":1,"description":"RAS like family 11 member B [Source:HGNC Symbol;Acc:HGNC:23804]"}, {"versioned_ensembl_gene_id":"ENSG00000188493.14","gene_symbol":"C19orf54","gene_name":"chromosome 19 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:24758]","synonyms":"FLJ41131","biotype":"protein_coding","ncbi_id":"284325","summary":null,"start":40740856,"end":40751553,"strand":-1,"description":"chromosome 19 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:24758]"}, {"versioned_ensembl_gene_id":"ENSG00000233849.1","gene_symbol":"AC022201.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70301451,"end":70302072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248518.1","gene_symbol":"AC098587.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54376002,"end":54376752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102753.9","gene_symbol":"KPNA3","gene_name":"karyopherin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6396]","synonyms":"SRP4,SRP1gamma,IPOA4,hSRP1","biotype":"protein_coding","ncbi_id":"3839","summary":"The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC), which consists of 60-100 proteins. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion while larger molecules are transported by an active process. The protein encoded by this gene belongs to the importin alpha family, and is involved in nuclear protein import. [provided by RefSeq, Jan 2009]","start":49699307,"end":49792921,"strand":-1,"description":"karyopherin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6396]"}, {"versioned_ensembl_gene_id":"ENSG00000276436.1","gene_symbol":"AL136301.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49792886,"end":49793307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228238.1","gene_symbol":"AL096803.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":186578279,"end":186579299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225527.1","gene_symbol":"AL450384.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18531849,"end":18533336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102245.7","gene_symbol":"CD40LG","gene_name":"CD40 ligand [Source:HGNC Symbol;Acc:HGNC:11935]","synonyms":"CD40L,CD154,TRAP,TNFSF5,IMD3,HIGM1,hCD40L,gp39","biotype":"protein_coding","ncbi_id":"959","summary":"The protein encoded by this gene is expressed on the surface of T cells. It regulates B cell function by engaging CD40 on the B cell surface. A defect in this gene results in an inability to undergo immunoglobulin class switch and is associated with hyper-IgM syndrome. [provided by RefSeq, Jul 2008]","start":136648193,"end":136660390,"strand":1,"description":"CD40 ligand [Source:HGNC Symbol;Acc:HGNC:11935]"}, {"versioned_ensembl_gene_id":"ENSG00000206290.10","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"DFNB53,DFNA13,HKE5","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33091492,"end":33121309,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000180259.9","gene_symbol":"PRNT","gene_name":"prion locus lncRNA, testis expressed [Source:HGNC Symbol;Acc:HGNC:18046]","synonyms":"M8","biotype":"protein_coding","ncbi_id":"149830","summary":null,"start":4731282,"end":4740668,"strand":-1,"description":"prion locus lncRNA, testis expressed [Source:HGNC Symbol;Acc:HGNC:18046]"}, {"versioned_ensembl_gene_id":"ENSG00000222004.7","gene_symbol":"C7orf71","gene_name":"chromosome 7 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:22364]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285941","summary":null,"start":26637871,"end":26647305,"strand":1,"description":"chromosome 7 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:22364]"}, {"versioned_ensembl_gene_id":"ENSG00000235045.2","gene_symbol":"RPL7P8","gene_name":"ribosomal protein L7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441896","summary":null,"start":109651370,"end":109652099,"strand":1,"description":"ribosomal protein L7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35914]"}, {"versioned_ensembl_gene_id":"ENSG00000224688.1","gene_symbol":"E2F6P2","gene_name":"E2F transcription factor 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"376818","summary":null,"start":21141624,"end":21142371,"strand":-1,"description":"E2F transcription factor 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51450]"}, {"versioned_ensembl_gene_id":"ENSG00000226708.1","gene_symbol":"AC073409.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123443266,"end":123444445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213085.9","gene_symbol":"CFAP45","gene_name":"cilia and flagella associated protein 45 [Source:HGNC Symbol;Acc:HGNC:17229]","synonyms":"NESG1,CCDC19","biotype":"protein_coding","ncbi_id":"25790","summary":null,"start":159872364,"end":159900163,"strand":-1,"description":"cilia and flagella associated protein 45 [Source:HGNC Symbol;Acc:HGNC:17229]"}, {"versioned_ensembl_gene_id":"ENSG00000250669.1","gene_symbol":"AC112206.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67690033,"end":67690437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174937.4","gene_symbol":"OR5M3","gene_name":"olfactory receptor family 5 subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:14806]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219482","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56469274,"end":56473352,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:14806]"}, {"versioned_ensembl_gene_id":"ENSG00000178028.13","gene_symbol":"DMAP1","gene_name":"DNA methyltransferase 1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18291]","synonyms":"KIAA1425,EAF2,FLJ11543,DNMTAP1,DNMAP1,SWC4,MEAF2","biotype":"protein_coding","ncbi_id":"55929","summary":"This gene encodes a subunit of several, distinct complexes involved in the repression or activation of transcription. The encoded protein can independently repress transcription and is targeted to replication foci throughout S phase by interacting directly with the N-terminus of DNA methyltransferase 1. During late S phase, histone deacetylase 2 is added to this complex, providing a means to deacetylate histones in transcriptionally inactive heterochromatin following replication. The encoded protein is also a component of the nucleosome acetyltransferase of H4 complex and interacts with the transcriptional corepressor tumor susceptibility gene 101 and the pro-apoptotic death-associated protein 6, among others. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":44213455,"end":44220681,"strand":1,"description":"DNA methyltransferase 1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18291]"}, {"versioned_ensembl_gene_id":"ENSG00000284732.1","gene_symbol":"AP002512.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56459221,"end":56473352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160087.20","gene_symbol":"UBE2J2","gene_name":"ubiquitin conjugating enzyme E2 J2 [Source:HGNC Symbol;Acc:HGNC:19268]","synonyms":"Ubc6p,NCUBE2","biotype":"protein_coding","ncbi_id":"118424","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is located in the membrane of the endoplasmic reticulum. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]","start":1253909,"end":1273885,"strand":-1,"description":"ubiquitin conjugating enzyme E2 J2 [Source:HGNC Symbol;Acc:HGNC:19268]"}, {"versioned_ensembl_gene_id":"ENSG00000143994.13","gene_symbol":"ABHD1","gene_name":"abhydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17553]","synonyms":"LABH1,FLJ36128","biotype":"protein_coding","ncbi_id":"84696","summary":"This gene is a member of the AB hydrolase superfamily and encodes a protein with an alpha/beta hydrolase fold. This domain is common to a number of hydrolytic enzymes of widely differing phylogenetic origins and catalytic functions. [provided by RefSeq, Jul 2008]","start":27123789,"end":27130812,"strand":1,"description":"abhydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17553]"}, {"versioned_ensembl_gene_id":"ENSG00000275024.1","gene_symbol":"AC005383.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114280725,"end":114281258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197468.5","gene_symbol":"AC073648.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8949630,"end":8950559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270996.1","gene_symbol":"AC005034.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75719120,"end":75720018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249312.1","gene_symbol":"ARL2BPP4","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130265","summary":null,"start":130529419,"end":130529889,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39448]"}, {"versioned_ensembl_gene_id":"ENSG00000225188.1","gene_symbol":"BX908738.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29223980,"end":29267066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236109.1","gene_symbol":"AC013402.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104583152,"end":104585354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214300.7","gene_symbol":"SPDYE3","gene_name":"speedy/RINGO cell cycle regulator family member E3 [Source:HGNC Symbol;Acc:HGNC:35462]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441272","summary":null,"start":100307702,"end":100322196,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E3 [Source:HGNC Symbol;Acc:HGNC:35462]"}, {"versioned_ensembl_gene_id":"ENSG00000270444.1","gene_symbol":"AZU1P1","gene_name":"azurocidin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49098]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480244","summary":null,"start":39856710,"end":39857094,"strand":-1,"description":"azurocidin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49098]"}, {"versioned_ensembl_gene_id":"ENSG00000253634.1","gene_symbol":"AC091096.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92565443,"end":92655494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110680.12","gene_symbol":"CALCA","gene_name":"calcitonin related polypeptide alpha [Source:HGNC Symbol;Acc:HGNC:1437]","synonyms":"CALC1","biotype":"protein_coding","ncbi_id":"796","summary":"This gene encodes the peptide hormones calcitonin, calcitonin gene-related peptide and katacalcin by tissue-specific alternative RNA splicing of the gene transcripts and cleavage of inactive precursor proteins. Calcitonin is involved in calcium regulation and acts to regulate phosphorus metabolism. Calcitonin gene-related peptide functions as a vasodilator and as an antimicrobial peptide while katacalcin is a calcium-lowering peptide. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2014]","start":14966668,"end":14972354,"strand":-1,"description":"calcitonin related polypeptide alpha [Source:HGNC Symbol;Acc:HGNC:1437]"}, {"versioned_ensembl_gene_id":"ENSG00000282206.1","gene_symbol":"AC233280.19","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":195635188,"end":195636301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175595.14","gene_symbol":"ERCC4","gene_name":"ERCC excision repair 4, endonuclease catalytic subunit [Source:HGNC Symbol;Acc:HGNC:3436]","synonyms":"XPF,RAD1,FANCQ","biotype":"protein_coding","ncbi_id":"2072","summary":"The protein encoded by this gene forms a complex with ERCC1 and is involved in the 5' incision made during nucleotide excision repair. This complex is a structure specific DNA repair endonuclease that interacts with EME1. Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F), or xeroderma pigmentosum VI (XP6).[provided by RefSeq, Mar 2009]","start":13920157,"end":13952345,"strand":1,"description":"ERCC excision repair 4, endonuclease catalytic subunit [Source:HGNC Symbol;Acc:HGNC:3436]"}, {"versioned_ensembl_gene_id":"ENSG00000197233.7","gene_symbol":"OR1J2","gene_name":"olfactory receptor family 1 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8209]","synonyms":"OST044,OR1J5,OR1J3","biotype":"protein_coding","ncbi_id":"26740","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122510802,"end":122511743,"strand":1,"description":"olfactory receptor family 1 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8209]"}, {"versioned_ensembl_gene_id":"ENSG00000163064.6","gene_symbol":"EN1","gene_name":"engrailed homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3342]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2019","summary":"Homeobox-containing genes are thought to have a role in controlling development. In Drosophila, the 'engrailed' (en) gene plays an important role during development in segmentation, where it is required for the formation of posterior compartments. Different mutations in the mouse homologs, En1 and En2, produced different developmental defects that frequently are lethal. The human engrailed homologs 1 and 2 encode homeodomain-containing proteins and have been implicated in the control of pattern formation during development of the central nervous system. [provided by RefSeq, Jul 2008]","start":118842171,"end":118847678,"strand":-1,"description":"engrailed homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3342]"}, {"versioned_ensembl_gene_id":"ENSG00000248610.1","gene_symbol":"HSPA8P4","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420028","summary":null,"start":130140031,"end":130141950,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44919]"}, {"versioned_ensembl_gene_id":"ENSG00000280236.3","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"polymorphic_pseudogene","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29395631,"end":29398008,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000232037.3","gene_symbol":"AL590556.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21908098,"end":21908580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236121.1","gene_symbol":"HAUS6P2","gene_name":"HAUS augmin like complex subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133268","summary":null,"start":31341371,"end":31344471,"strand":-1,"description":"HAUS augmin like complex subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43765]"}, {"versioned_ensembl_gene_id":"ENSG00000249103.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29417201,"end":29418163,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000215545.1","gene_symbol":"DEFB116","gene_name":"defensin beta 116 [Source:HGNC Symbol;Acc:HGNC:18097]","synonyms":"DEFB-16","biotype":"protein_coding","ncbi_id":"245930","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. [provided by RefSeq, Oct 2014]","start":31303212,"end":31308585,"strand":-1,"description":"defensin beta 116 [Source:HGNC Symbol;Acc:HGNC:18097]"}, {"versioned_ensembl_gene_id":"ENSG00000267124.2","gene_symbol":"AC016588.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":305573,"end":306467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274437.4","gene_symbol":"DERL3","gene_name":"derlin 3 [Source:HGNC Symbol;Acc:HGNC:14236]","synonyms":"derlin-3,C22orf14,MGC71803,IZP6,FLJ43842","biotype":"protein_coding","ncbi_id":"91319","summary":"The protein encoded by this gene belongs to the derlin family, and resides in the endoplasmic reticulum (ER). Proteins that are unfolded or misfolded in the ER must be refolded or degraded to maintain the homeostasis of the ER. This protein appears to be involved in the degradation of misfolded glycoproteins in the ER. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008]","start":23834503,"end":23839128,"strand":-1,"description":"derlin 3 [Source:HGNC Symbol;Acc:HGNC:14236]"}, {"versioned_ensembl_gene_id":"ENSG00000235263.1","gene_symbol":"AL928921.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9501092,"end":9503471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261761.3","gene_symbol":"AL136537.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":37001816,"end":37020708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229412.5","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439235,"end":29440906,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000262235.2","gene_symbol":"TMF1P1","gene_name":"TATA element modulatory factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51353]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480320","summary":null,"start":13458326,"end":13458698,"strand":1,"description":"TATA element modulatory factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51353]"}, {"versioned_ensembl_gene_id":"ENSG00000189058.8","gene_symbol":"APOD","gene_name":"apolipoprotein D [Source:HGNC Symbol;Acc:HGNC:612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347","summary":"This gene encodes a component of high density lipoprotein that has no marked similarity to other apolipoprotein sequences. It has a high degree of homology to plasma retinol-binding protein and other members of the alpha 2 microglobulin protein superfamily of carrier proteins, also known as lipocalins. This glycoprotein is closely associated with the enzyme lecithin:cholesterol acyltransferase - an enzyme involved in lipoprotein metabolism. [provided by RefSeq, Aug 2008]","start":195568702,"end":195584205,"strand":-1,"description":"apolipoprotein D [Source:HGNC Symbol;Acc:HGNC:612]"}, {"versioned_ensembl_gene_id":"ENSG00000227446.2","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"protein_coding","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29396471,"end":29397539,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000278289.4","gene_symbol":"CT45A6","gene_name":"cancer/testis antigen family 45 member A6 [Source:HGNC Symbol;Acc:HGNC:33271]","synonyms":"CT45.6,CT45-6","biotype":"protein_coding","ncbi_id":"541465","summary":null,"start":135794706,"end":135802656,"strand":-1,"description":"cancer/testis antigen family 45 member A6 [Source:HGNC Symbol;Acc:HGNC:33271]"}, {"versioned_ensembl_gene_id":"ENSG00000279687.1","gene_symbol":"FP565260.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5073458,"end":5087867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230578.3","gene_symbol":"AC234781.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155348752,"end":155349799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229242.1","gene_symbol":"AL358452.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":215886582,"end":215901464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213172.3","gene_symbol":"AL031985.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40364766,"end":40365183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254947.1","gene_symbol":"OR8K4P","gene_name":"olfactory receptor family 8 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15314]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81166","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56142516,"end":56143387,"strand":-1,"description":"olfactory receptor family 8 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15314]"}, {"versioned_ensembl_gene_id":"ENSG00000165462.5","gene_symbol":"PHOX2A","gene_name":"paired like homeobox 2a [Source:HGNC Symbol;Acc:HGNC:691]","synonyms":"PMX2A,FEOM2,CFEOM2,ARIX","biotype":"protein_coding","ncbi_id":"401","summary":"The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. [provided by RefSeq, Jul 2008]","start":72239077,"end":72245664,"strand":-1,"description":"paired like homeobox 2a [Source:HGNC Symbol;Acc:HGNC:691]"}, {"versioned_ensembl_gene_id":"ENSG00000228299.9","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31260956,"end":31264327,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000284693.1","gene_symbol":"AL928921.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9425094,"end":9440564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148123.14","gene_symbol":"PLPPR1","gene_name":"phospholipid phosphatase related 1 [Source:HGNC Symbol;Acc:HGNC:25993]","synonyms":"LPPR1,FLJ20300,PRG-3,MGC26189","biotype":"protein_coding","ncbi_id":"54886","summary":"This gene encodes a member of the plasticity-related gene (PRG) family. Members of the PRG family mediate lipid phosphate phosphatase activity in neurons and are known to be involved in neuronal plasticity. The protein encoded by this gene does not perform its function through enzymatic phospholipid degradation. This gene is strongly expressed in brain. It shows dynamic expression regulation during brain development and neuronal excitation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":101028709,"end":101325135,"strand":1,"description":"phospholipid phosphatase related 1 [Source:HGNC Symbol;Acc:HGNC:25993]"}, {"versioned_ensembl_gene_id":"ENSG00000166856.2","gene_symbol":"GPR182","gene_name":"G protein-coupled receptor 182 [Source:HGNC Symbol;Acc:HGNC:13708]","synonyms":"hrhAMR,G10D,AM-R,ADMR","biotype":"protein_coding","ncbi_id":"11318","summary":"Adrenomedullin is a potent vasodilator peptide that exerts major effects on cardiovascular function. This gene encodes a seven-transmembrane protein that belongs to the family 1 of G-protein coupled receptors. Studies of the rat counterpart suggest that the encoded protein may function as a receptor for adrenomedullin. [provided by RefSeq, Jul 2008]","start":56994446,"end":56998441,"strand":1,"description":"G protein-coupled receptor 182 [Source:HGNC Symbol;Acc:HGNC:13708]"}, {"versioned_ensembl_gene_id":"ENSG00000163110.14","gene_symbol":"PDLIM5","gene_name":"PDZ and LIM domain 5 [Source:HGNC Symbol;Acc:HGNC:17468]","synonyms":"LIM,Enh","biotype":"protein_coding","ncbi_id":"10611","summary":"This gene encodes a member of a family of proteins that possess a 100-amino acid PDZ domain at the N terminus and one to three LIM domains at the C-terminus. This family member functions as a scaffold protein that tethers protein kinases to the Z-disk in striated muscles. It is thought to function in cardiomyocyte expansion and in restraining postsynaptic growth of excitatory synapses. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":94451857,"end":94668227,"strand":1,"description":"PDZ and LIM domain 5 [Source:HGNC Symbol;Acc:HGNC:17468]"}, {"versioned_ensembl_gene_id":"ENSG00000270362.1","gene_symbol":"HMGN3-AS1","gene_name":"HMGN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48984]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288198","summary":null,"start":79233718,"end":79236797,"strand":1,"description":"HMGN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48984]"}, {"versioned_ensembl_gene_id":"ENSG00000250159.6","gene_symbol":"AC106791.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137814333,"end":137889336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169484.3","gene_symbol":"OR4K14","gene_name":"olfactory receptor family 4 subfamily K member 14 [Source:HGNC Symbol;Acc:HGNC:15352]","synonyms":null,"biotype":"protein_coding","ncbi_id":"122740","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20014143,"end":20019307,"strand":-1,"description":"olfactory receptor family 4 subfamily K member 14 [Source:HGNC Symbol;Acc:HGNC:15352]"}, {"versioned_ensembl_gene_id":"ENSG00000260004.1","gene_symbol":"AC092138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65601101,"end":65601698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243243.5","gene_symbol":"AC073130.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116237929,"end":116327896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245832.6","gene_symbol":"MIR4300HG","gene_name":"MIR4300 host gene [Source:HGNC Symbol;Acc:HGNC:52003]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928989","summary":null,"start":81879851,"end":82718082,"strand":-1,"description":"MIR4300 host gene [Source:HGNC Symbol;Acc:HGNC:52003]"}, {"versioned_ensembl_gene_id":"ENSG00000149133.1","gene_symbol":"OR5F1","gene_name":"olfactory receptor family 5 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:8343]","synonyms":"OR11-10","biotype":"protein_coding","ncbi_id":"338674","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55993681,"end":55994625,"strand":-1,"description":"olfactory receptor family 5 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:8343]"}, {"versioned_ensembl_gene_id":"ENSG00000280347.1","gene_symbol":"AC000123.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127359785,"end":127364759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178395.6","gene_symbol":"CCDC185","gene_name":"coiled-coil domain containing 185 [Source:HGNC Symbol;Acc:HGNC:26654]","synonyms":"FLJ35728,C1orf65","biotype":"protein_coding","ncbi_id":"164127","summary":null,"start":223393417,"end":223395470,"strand":1,"description":"coiled-coil domain containing 185 [Source:HGNC Symbol;Acc:HGNC:26654]"}, {"versioned_ensembl_gene_id":"ENSG00000105855.9","gene_symbol":"ITGB8","gene_name":"integrin subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:6163]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3696","summary":"This gene is a member of the integrin beta chain family and encodes a single-pass type I membrane protein with a VWFA domain and four cysteine-rich repeats. This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex. In general, integrin complexes mediate cell-cell and cell-extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":20330702,"end":20415754,"strand":1,"description":"integrin subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:6163]"}, {"versioned_ensembl_gene_id":"ENSG00000226896.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"HS6M1-14,OR2I2,OR2I4P,OR2I1,OR2I3P","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29553320,"end":29554267,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000227576.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"dJ271M21.8,PsiGPR53","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537778,"end":29538861,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000275773.1","gene_symbol":"AL590227.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60723148,"end":60723898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283453.1","gene_symbol":"AC244258.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60281444,"end":60544955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270316.1","gene_symbol":"BORCS7-ASMT","gene_name":"BORCS7-ASMT readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49183]","synonyms":"C10orf32-ASMT","biotype":"protein_coding","ncbi_id":"100528007","summary":"This locus represents naturally occurring read-through transcription between the neighboring C10orf32 (chromosome 10 open reading frame 32) and AS3MT (arsenic, +3 oxidation state, methyltransferase) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":102854272,"end":102901899,"strand":1,"description":"BORCS7-ASMT readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49183]"}, {"versioned_ensembl_gene_id":"ENSG00000234920.3","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G2,NG38,ATP6G,Em:AC004181.3,Vma10","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31535211,"end":31537597,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000176956.12","gene_symbol":"LY6H","gene_name":"lymphocyte antigen 6 family member H [Source:HGNC Symbol;Acc:HGNC:6728]","synonyms":"NMLY6","biotype":"protein_coding","ncbi_id":"4062","summary":null,"start":143157914,"end":143160711,"strand":-1,"description":"lymphocyte antigen 6 family member H [Source:HGNC Symbol;Acc:HGNC:6728]"}, {"versioned_ensembl_gene_id":"ENSG00000233561.6","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DBP2,Prp2,DDX16,PRPF2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30642952,"end":30662900,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000237510.7","gene_symbol":"GPAT2P1","gene_name":"glycerol-3-phosphate acyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52330]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643219","summary":null,"start":95789654,"end":95800166,"strand":1,"description":"glycerol-3-phosphate acyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52330]"}, {"versioned_ensembl_gene_id":"ENSG00000051180.16","gene_symbol":"RAD51","gene_name":"RAD51 recombinase [Source:HGNC Symbol;Acc:HGNC:9817]","synonyms":"RECA,RAD51A,HsT16930,HsRad51,FANCR,BRCC5","biotype":"protein_coding","ncbi_id":"5888","summary":"The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51, and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with the ssDNA-binding protein RPA and RAD52, and it is thought to play roles in homologous pairing and strand transfer of DNA. This protein is also found to interact with BRCA1 and BRCA2, which may be important for the cellular response to DNA damage. BRCA2 is shown to regulate both the intracellular localization and DNA-binding ability of this protein. Loss of these controls following BRCA2 inactivation may be a key event leading to genomic instability and tumorigenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":40694774,"end":40732339,"strand":1,"description":"RAD51 recombinase [Source:HGNC Symbol;Acc:HGNC:9817]"}, {"versioned_ensembl_gene_id":"ENSG00000184113.9","gene_symbol":"CLDN5","gene_name":"claudin 5 [Source:HGNC Symbol;Acc:HGNC:2047]","synonyms":"TMVCF,CPETRL1,BEC1,AWAL","biotype":"protein_coding","ncbi_id":"7122","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Mutations in this gene have been found in patients with velocardiofacial syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018]","start":19523024,"end":19527545,"strand":-1,"description":"claudin 5 [Source:HGNC Symbol;Acc:HGNC:2047]"}, {"versioned_ensembl_gene_id":"ENSG00000236662.1","gene_symbol":"AL133215.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100980507,"end":100985614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182325.10","gene_symbol":"FBXL6","gene_name":"F-box and leucine rich repeat protein 6 [Source:HGNC Symbol;Acc:HGNC:13603]","synonyms":"FBL6","biotype":"protein_coding","ncbi_id":"26233","summary":"This gene encodes a member of a family of proteins that are characterized by an F-box motif. The encoded protein also contains leucine-rich repeats. F-box-containing proteins comprise one of the subunits of the SCF (SKP1-cullin-F-box) complex, which functions in phosphorylation-dependent ubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":144355431,"end":144359376,"strand":-1,"description":"F-box and leucine rich repeat protein 6 [Source:HGNC Symbol;Acc:HGNC:13603]"}, {"versioned_ensembl_gene_id":"ENSG00000254500.1","gene_symbol":"RANP3","gene_name":"RAN, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39858]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874227","summary":null,"start":74652636,"end":74652911,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39858]"}, {"versioned_ensembl_gene_id":"ENSG00000234160.1","gene_symbol":"AL513165.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37509150,"end":37510299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270257.1","gene_symbol":"AC096720.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67638177,"end":67638359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096746.17","gene_symbol":"HNRNPH3","gene_name":"heterogeneous nuclear ribonucleoprotein H3 [Source:HGNC Symbol;Acc:HGNC:5043]","synonyms":"HNRPH3,2H9","biotype":"protein_coding","ncbi_id":"3189","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two repeats of quasi-RRM domains that bind to RNAs. It is localized in nuclear bodies of the nucleus. This protein is involved in the splicing process and it also participates in early heat shock-induced splicing arrest by transiently leaving the hnRNP complexes. Several alternatively spliced transcript variants have been noted for this gene, however, not all are fully characterized. [provided by RefSeq, Jul 2008]","start":68331174,"end":68343191,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein H3 [Source:HGNC Symbol;Acc:HGNC:5043]"}, {"versioned_ensembl_gene_id":"ENSG00000283625.1","gene_symbol":"AC128714.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":184499484,"end":184500370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268324.2","gene_symbol":"LRRC2-AS1","gene_name":"LRRC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:15571]","synonyms":"LUZPP1,LUZP3P,LUZP3","biotype":"antisense_RNA","ncbi_id":"83598","summary":null,"start":46557398,"end":46559694,"strand":1,"description":"LRRC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:15571]"}, {"versioned_ensembl_gene_id":"ENSG00000283352.1","gene_symbol":"AL021368.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":57919912,"end":57961382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218189.4","gene_symbol":"POM121L14P","gene_name":"POM121 transmembrane nucleoporin like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44414]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727805","summary":null,"start":57937458,"end":57939015,"strand":1,"description":"POM121 transmembrane nucleoporin like 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:44414]"}, {"versioned_ensembl_gene_id":"ENSG00000103168.16","gene_symbol":"TAF1C","gene_name":"TATA-box binding protein associated factor, RNA polymerase I subunit C [Source:HGNC Symbol;Acc:HGNC:11534]","synonyms":"TAFI95,TAFI110,SL1,MGC:39976","biotype":"protein_coding","ncbi_id":"9013","summary":"Initiation of transcription by RNA polymerase I requires the formation of a complex composed of the TATA-binding protein (TBP) and three TBP-associated factors (TAFs) specific for RNA polymerase I. This complex, known as SL1, binds to the core promoter of ribosomal RNA genes to position the polymerase properly and acts as a channel for regulatory signals. This gene encodes the largest SL1-specific TAF. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2011]","start":84177847,"end":84187070,"strand":-1,"description":"TATA-box binding protein associated factor, RNA polymerase I subunit C [Source:HGNC Symbol;Acc:HGNC:11534]"}, {"versioned_ensembl_gene_id":"ENSG00000122565.18","gene_symbol":"CBX3","gene_name":"chromobox 3 [Source:HGNC Symbol;Acc:HGNC:1553]","synonyms":"HP1Hs-gamma","biotype":"protein_coding","ncbi_id":"11335","summary":"At the nuclear envelope, the nuclear lamina and heterochromatin are adjacent to the inner nuclear membrane. The protein encoded by this gene binds DNA and is a component of heterochromatin. This protein also can bind lamin B receptor, an integral membrane protein found in the inner nuclear membrane. The dual binding functions of the encoded protein may explain the association of heterochromatin with the inner nuclear membrane. This protein binds histone H3 tails methylated at Lys-9 sites. This protein is also recruited to sites of ultraviolet-induced DNA damage and double-strand breaks. Two transcript variants encoding the same protein but differing in the 5' UTR, have been found for this gene.[provided by RefSeq, Mar 2011]","start":26201162,"end":26213356,"strand":1,"description":"chromobox 3 [Source:HGNC Symbol;Acc:HGNC:1553]"}, {"versioned_ensembl_gene_id":"ENSG00000226455.1","gene_symbol":"AL121787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89950116,"end":89953186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230477.1","gene_symbol":"AC005034.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75598071,"end":75598559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278872.1","gene_symbol":"AC148477.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132279256,"end":132280900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259767.1","gene_symbol":"AC022558.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":83022236,"end":83024336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230389.3","gene_symbol":"HCP5","gene_name":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]","synonyms":"D6S2650E,P5-1","biotype":"processed_transcript","ncbi_id":"10866","summary":null,"start":31453889,"end":31456523,"strand":1,"description":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]"}, {"versioned_ensembl_gene_id":"ENSG00000273333.2","gene_symbol":"AL662884.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":32184733,"end":32185882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280752.1","gene_symbol":"LINC00850","gene_name":"long intergenic non-protein coding RNA 850 [Source:HGNC Symbol;Acc:HGNC:45092]","synonyms":"KUCG1","biotype":"lincRNA","ncbi_id":"101241891","summary":null,"start":149825708,"end":149879799,"strand":1,"description":"long intergenic non-protein coding RNA 850 [Source:HGNC Symbol;Acc:HGNC:45092]"}, {"versioned_ensembl_gene_id":"ENSG00000276445.1","gene_symbol":"AC005393.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39812972,"end":39813555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152990.13","gene_symbol":"ADGRA3","gene_name":"adhesion G protein-coupled receptor A3 [Source:HGNC Symbol;Acc:HGNC:13839]","synonyms":"PGR21,GPR125,FLJ38547","biotype":"protein_coding","ncbi_id":"166647","summary":"This gene encodes a member of the G protein-coupled receptor superfamily. This membrane protein may play a role in tumor angiogenesis through its interaction with the human homolog of the Drosophila disc large tumor suppressor gene. This gene is mapped to a candidate region of chromosome 4 which may be associated with bipolar disorder and schizophrenia. [provided by RefSeq, Oct 2012]","start":22345071,"end":22516054,"strand":-1,"description":"adhesion G protein-coupled receptor A3 [Source:HGNC Symbol;Acc:HGNC:13839]"}, {"versioned_ensembl_gene_id":"ENSG00000228833.1","gene_symbol":"AC244098.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149757797,"end":149757895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217325.2","gene_symbol":"PRELID1P1","gene_name":"PRELI domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43886]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"728666","summary":null,"start":126643488,"end":126644390,"strand":1,"description":"PRELI domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43886]"}, {"versioned_ensembl_gene_id":"ENSG00000275953.1","gene_symbol":"AL359535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126627484,"end":126628570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206047.2","gene_symbol":"DEFA1","gene_name":"defensin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2761]","synonyms":"MRS,HNP-1,DEFA2,DEF1","biotype":"protein_coding","ncbi_id":"1667","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. The protein encoded by this gene, defensin, alpha 1, is found in the microbicidal granules of neutrophils and likely plays a role in phagocyte-mediated host defense. Several alpha defensin genes are clustered on chromosome 8. This gene differs from defensin, alpha 3 by only one amino acid. This gene and the gene encoding defensin, alpha 3 are both subject to copy number variation. [provided by RefSeq, Oct 2014]","start":6977649,"end":6980080,"strand":-1,"description":"defensin alpha 1 [Source:HGNC Symbol;Acc:HGNC:2761]"}, {"versioned_ensembl_gene_id":"ENSG00000259797.1","gene_symbol":"AC020978.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68316801,"end":68319036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230971.1","gene_symbol":"AC005703.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15267461,"end":15272290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233238.1","gene_symbol":"DEFA9P","gene_name":"defensin alpha 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:31800]","synonyms":"DEFAP2","biotype":"unprocessed_pseudogene","ncbi_id":"449492","summary":null,"start":6959289,"end":6960161,"strand":-1,"description":"defensin alpha 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:31800]"}, {"versioned_ensembl_gene_id":"ENSG00000279386.1","gene_symbol":"AC021106.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37866561,"end":37867091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196712.17","gene_symbol":"NF1","gene_name":"neurofibromin 1 [Source:HGNC Symbol;Acc:HGNC:7765]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4763","summary":"This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. [provided by RefSeq, Jul 2008]","start":31094927,"end":31382116,"strand":1,"description":"neurofibromin 1 [Source:HGNC Symbol;Acc:HGNC:7765]"}, {"versioned_ensembl_gene_id":"ENSG00000231877.1","gene_symbol":"AL359551.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":238485445,"end":238538305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225124.1","gene_symbol":"RPL23AP36","gene_name":"ribosomal protein L23a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35685]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271296","summary":null,"start":203074685,"end":203075142,"strand":-1,"description":"ribosomal protein L23a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35685]"}, {"versioned_ensembl_gene_id":"ENSG00000249963.1","gene_symbol":"EEF1A1P20","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37893]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421797","summary":null,"start":99996547,"end":99997932,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37893]"}, {"versioned_ensembl_gene_id":"ENSG00000091128.12","gene_symbol":"LAMB4","gene_name":"laminin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6491]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22798","summary":null,"start":108023548,"end":108130356,"strand":-1,"description":"laminin subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:6491]"}, {"versioned_ensembl_gene_id":"ENSG00000206355.11","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"C6orf18,HCR","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31136168,"end":31151940,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000077684.15","gene_symbol":"JADE1","gene_name":"jade family PHD finger 1 [Source:HGNC Symbol;Acc:HGNC:30027]","synonyms":"PHF17,JADE-1","biotype":"protein_coding","ncbi_id":"79960","summary":null,"start":128809623,"end":128875224,"strand":1,"description":"jade family PHD finger 1 [Source:HGNC Symbol;Acc:HGNC:30027]"}, {"versioned_ensembl_gene_id":"ENSG00000249551.1","gene_symbol":"LINC02216","gene_name":"long intergenic non-protein coding RNA 2216 [Source:HGNC Symbol;Acc:HGNC:53083]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379141","summary":null,"start":118575575,"end":118581324,"strand":1,"description":"long intergenic non-protein coding RNA 2216 [Source:HGNC Symbol;Acc:HGNC:53083]"}, {"versioned_ensembl_gene_id":"ENSG00000274594.1","gene_symbol":"AL391669.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138464099,"end":138464383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229549.9","gene_symbol":"TSPY8","gene_name":"testis specific protein, Y-linked 8 [Source:HGNC Symbol;Acc:HGNC:37471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728403","summary":null,"start":9357797,"end":9360599,"strand":1,"description":"testis specific protein, Y-linked 8 [Source:HGNC Symbol;Acc:HGNC:37471]"}, {"versioned_ensembl_gene_id":"ENSG00000145194.17","gene_symbol":"ECE2","gene_name":"endothelin converting enzyme 2 [Source:HGNC Symbol;Acc:HGNC:13275]","synonyms":"MGC2408,KIAA0604","biotype":"protein_coding","ncbi_id":"9718","summary":null,"start":184249650,"end":184293031,"strand":1,"description":"endothelin converting enzyme 2 [Source:HGNC Symbol;Acc:HGNC:13275]"}, {"versioned_ensembl_gene_id":"ENSG00000253513.1","gene_symbol":"AC009908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124996985,"end":124998198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146966.12","gene_symbol":"DENND2A","gene_name":"DENN domain containing 2A [Source:HGNC Symbol;Acc:HGNC:22212]","synonyms":"KIAA1277,FAM31D","biotype":"protein_coding","ncbi_id":"27147","summary":null,"start":140518420,"end":140673993,"strand":-1,"description":"DENN domain containing 2A [Source:HGNC Symbol;Acc:HGNC:22212]"}, {"versioned_ensembl_gene_id":"ENSG00000253544.1","gene_symbol":"C1GALT1P3","gene_name":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481730","summary":null,"start":61909984,"end":61910802,"strand":-1,"description":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51616]"}, {"versioned_ensembl_gene_id":"ENSG00000251477.1","gene_symbol":"AC114322.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117719240,"end":117722097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258748.1","gene_symbol":"AL359399.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104137150,"end":104137898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255018.1","gene_symbol":"AC022878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13152200,"end":13152348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196396.9","gene_symbol":"PTPN1","gene_name":"protein tyrosine phosphatase, non-receptor type 1 [Source:HGNC Symbol;Acc:HGNC:9642]","synonyms":"PTP1B","biotype":"protein_coding","ncbi_id":"5770","summary":"The protein encoded by this gene is the founding member of the protein tyrosine phosphatase (PTP) family, which was isolated and identified based on its enzymatic activity and amino acid sequence. PTPs catalyze the hydrolysis of the phosphate monoesters specifically on tyrosine residues. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP has been shown to act as a negative regulator of insulin signaling by dephosphorylating the phosphotryosine residues of insulin receptor kinase. This PTP was also reported to dephosphorylate epidermal growth factor receptor kinase, as well as JAK2 and TYK2 kinases, which implicated the role of this PTP in cell growth control, and cell response to interferon stimulation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":50510321,"end":50585241,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 1 [Source:HGNC Symbol;Acc:HGNC:9642]"}, {"versioned_ensembl_gene_id":"ENSG00000100442.10","gene_symbol":"FKBP3","gene_name":"FK506 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3719]","synonyms":"PPIase,FKBP-25","biotype":"protein_coding","ncbi_id":"2287","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin, as well as histone deacetylases, the transcription factor YY1, casein kinase II, and nucleolin. It has a higher affinity for rapamycin than for FK506 and thus may be an important target molecule for immunosuppression by rapamycin. [provided by RefSeq, Sep 2008]","start":45115600,"end":45135319,"strand":-1,"description":"FK506 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:3719]"}, {"versioned_ensembl_gene_id":"ENSG00000120451.10","gene_symbol":"SNX19","gene_name":"sorting nexin 19 [Source:HGNC Symbol;Acc:HGNC:21532]","synonyms":"KIAA0254,CHET8","biotype":"protein_coding","ncbi_id":"399979","summary":"Islet antigen-2 (IA-2) is an autoantigen in type 1 diabetes and plays a role in insulin secretion. IA-2 is found in dense-core secretory vesicles and interacts with the product of this gene, a sorting nexin. In mouse pancreatic beta-cells, the encoded protein influenced insulin secretion by stabilizing the number of dense-core secretory vesicles. [provided by RefSeq, Dec 2016]","start":130875436,"end":130916509,"strand":-1,"description":"sorting nexin 19 [Source:HGNC Symbol;Acc:HGNC:21532]"}, {"versioned_ensembl_gene_id":"ENSG00000242856.3","gene_symbol":"VN1R105P","gene_name":"vomeronasal 1 receptor 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:37428]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100288264","summary":null,"start":54647944,"end":54648853,"strand":1,"description":"vomeronasal 1 receptor 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:37428]"}, {"versioned_ensembl_gene_id":"ENSG00000125149.11","gene_symbol":"C16orf70","gene_name":"chromosome 16 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:29564]","synonyms":"LIN10,lin-10,FLJ12076,C16orf6","biotype":"protein_coding","ncbi_id":"80262","summary":null,"start":67109958,"end":67148539,"strand":1,"description":"chromosome 16 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:29564]"}, {"versioned_ensembl_gene_id":"ENSG00000099326.8","gene_symbol":"MZF1","gene_name":"myeloid zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13108]","synonyms":"ZSCAN6,ZNF42,Zfp98,MZF1B,MZF-1","biotype":"protein_coding","ncbi_id":"7593","summary":null,"start":58561931,"end":58573575,"strand":-1,"description":"myeloid zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13108]"}, {"versioned_ensembl_gene_id":"ENSG00000010072.15","gene_symbol":"SPRTN","gene_name":"SprT-like N-terminal domain [Source:HGNC Symbol;Acc:HGNC:25356]","synonyms":"Spartan,DVC1,DKFZP547N043,C1orf124","biotype":"protein_coding","ncbi_id":"83932","summary":"The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]","start":231337104,"end":231355023,"strand":1,"description":"SprT-like N-terminal domain [Source:HGNC Symbol;Acc:HGNC:25356]"}, {"versioned_ensembl_gene_id":"ENSG00000226862.1","gene_symbol":"AC104463.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":202604268,"end":202605293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236616.3","gene_symbol":"BAK1P2","gene_name":"BCL2 antagonist/killer 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:997]","synonyms":"BCL2L7P2,BAK3P,BAK3","biotype":"processed_pseudogene","ncbi_id":"601","summary":null,"start":130546799,"end":130547429,"strand":-1,"description":"BCL2 antagonist/killer 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:997]"}, {"versioned_ensembl_gene_id":"ENSG00000117899.10","gene_symbol":"MESD","gene_name":"mesoderm development LRP chaperone [Source:HGNC Symbol;Acc:HGNC:13520]","synonyms":"KIAA0081,BOCA,MESDC2","biotype":"protein_coding","ncbi_id":"23184","summary":null,"start":80946289,"end":80989878,"strand":-1,"description":"mesoderm development LRP chaperone [Source:HGNC Symbol;Acc:HGNC:13520]"}, {"versioned_ensembl_gene_id":"ENSG00000254336.1","gene_symbol":"AC008694.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157604707,"end":157605637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269420.5","gene_symbol":"PLA2G4C-AS1","gene_name":"PLA2G4C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51585]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106144526","summary":null,"start":48061371,"end":48064945,"strand":1,"description":"PLA2G4C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51585]"}, {"versioned_ensembl_gene_id":"ENSG00000110427.14","gene_symbol":"KIAA1549L","gene_name":"KIAA1549 like [Source:HGNC Symbol;Acc:HGNC:24836]","synonyms":"MGC34830,G2,C11orf69,C11orf41","biotype":"protein_coding","ncbi_id":"25758","summary":null,"start":33542072,"end":33674102,"strand":1,"description":"KIAA1549 like [Source:HGNC Symbol;Acc:HGNC:24836]"}, {"versioned_ensembl_gene_id":"ENSG00000249045.1","gene_symbol":"MTND3P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52170]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075199","summary":null,"start":64610980,"end":64611308,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52170]"}, {"versioned_ensembl_gene_id":"ENSG00000161973.10","gene_symbol":"CCDC42","gene_name":"coiled-coil domain containing 42 [Source:HGNC Symbol;Acc:HGNC:26528]","synonyms":"FLJ32734,CCDC42A","biotype":"protein_coding","ncbi_id":"146849","summary":null,"start":8729934,"end":8745219,"strand":-1,"description":"coiled-coil domain containing 42 [Source:HGNC Symbol;Acc:HGNC:26528]"}, {"versioned_ensembl_gene_id":"ENSG00000274113.4","gene_symbol":"LILRA5","gene_name":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]","synonyms":"CD85,LILRB7,ILT11,CD85f,LIR9","biotype":"protein_coding","ncbi_id":"353514","summary":"The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":54315100,"end":54321156,"strand":-1,"description":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]"}, {"versioned_ensembl_gene_id":"ENSG00000279073.3","gene_symbol":"AL807752.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":137031241,"end":137040436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267481.1","gene_symbol":"AC011477.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19788755,"end":19790531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230342.2","gene_symbol":"FANCD2P2","gene_name":"Fanconi anemia complementation group D2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44488]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101929530","summary":null,"start":11859674,"end":11891172,"strand":1,"description":"Fanconi anemia complementation group D2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44488]"}, {"versioned_ensembl_gene_id":"ENSG00000268088.1","gene_symbol":"AC093063.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39693925,"end":39696258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260951.1","gene_symbol":"AC003985.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25358240,"end":25359908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126785.12","gene_symbol":"RHOJ","gene_name":"ras homolog family member J [Source:HGNC Symbol;Acc:HGNC:688]","synonyms":"TCL,RASL7B,FLJ14445,ARHJ","biotype":"protein_coding","ncbi_id":"57381","summary":"This gene encodes one of the many small GTP-binding proteins in the Rho family shown to be associated with focal adhesions in endothelial cells (PMID: 21148427, 22103495). The encoded protein is activated by vascular endothelial growth factor and may regulate angiogenesis. [provided by RefSeq, Dec 2011]","start":63204114,"end":63293219,"strand":1,"description":"ras homolog family member J [Source:HGNC Symbol;Acc:HGNC:688]"}, {"versioned_ensembl_gene_id":"ENSG00000254806.5","gene_symbol":"SYS1-DBNDD2","gene_name":"SYS1-DBNDD2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33535]","synonyms":null,"biotype":"protein_coding","ncbi_id":"767557","summary":"This locus represents naturally occurring read-through transcription from the neighboring SYS1 Golgi-localized integral membrane protein homolog and dysbindin domain containing 2 (DBNDD2) genes. The read-through transcript includes the majority of exons from each individual gene, but it would be subject to nonsense-mediated mRNA decay (NMD) and is therefore predicted to be non-coding. [provided by RefSeq, Oct 2010]","start":45363200,"end":45410610,"strand":1,"description":"SYS1-DBNDD2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:33535]"}, {"versioned_ensembl_gene_id":"ENSG00000065457.10","gene_symbol":"ADAT1","gene_name":"adenosine deaminase, tRNA specific 1 [Source:HGNC Symbol;Acc:HGNC:228]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23536","summary":"This gene is a member of the ADAR (adenosine deaminase acting on RNA) family. Using site-specific adenosine modification, proteins encoded by these genes participate in the pre-mRNA editing of nuclear transcripts. The protein encoded by this gene, tRNA-specific adenosine deaminase 1, is responsible for the deamination of adenosine 37 to inosine in eukaryotic tRNA. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2010]","start":75596981,"end":75623300,"strand":-1,"description":"adenosine deaminase, tRNA specific 1 [Source:HGNC Symbol;Acc:HGNC:228]"}, {"versioned_ensembl_gene_id":"ENSG00000167670.15","gene_symbol":"CHAF1A","gene_name":"chromatin assembly factor 1 subunit A [Source:HGNC Symbol;Acc:HGNC:1910]","synonyms":"P150,MGC71229,CAF1P150,CAF1B,CAF1,CAF-1","biotype":"protein_coding","ncbi_id":"10036","summary":"Chromatin assembly factor I (CAF1) is a nuclear complex consisting of p50, p60 (CHAF1B; MIM 601245), and p150 (CHAF1A) subunits that assembles histone octamers onto replicating DNA in vitro (Kaufman et al., 1995 [PubMed 7600578]).[supplied by OMIM, Mar 2008]","start":4402662,"end":4445018,"strand":1,"description":"chromatin assembly factor 1 subunit A [Source:HGNC Symbol;Acc:HGNC:1910]"}, {"versioned_ensembl_gene_id":"ENSG00000204471.3","gene_symbol":"TBC1D3P4","gene_name":"TBC1 domain family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32409]","synonyms":"USP6P2","biotype":"unprocessed_pseudogene","ncbi_id":"100631253","summary":null,"start":18393480,"end":18400961,"strand":1,"description":"TBC1 domain family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32409]"}, {"versioned_ensembl_gene_id":"ENSG00000145879.10","gene_symbol":"SPINK7","gene_name":"serine peptidase inhibitor, Kazal type 7 (putative) [Source:HGNC Symbol;Acc:HGNC:24643]","synonyms":"ECRG2,ECG2","biotype":"protein_coding","ncbi_id":"84651","summary":null,"start":148312419,"end":148315922,"strand":1,"description":"serine peptidase inhibitor, Kazal type 7 (putative) [Source:HGNC Symbol;Acc:HGNC:24643]"}, {"versioned_ensembl_gene_id":"ENSG00000258120.1","gene_symbol":"KRT128P","gene_name":"keratin 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:48882]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480238","summary":null,"start":52632866,"end":52634456,"strand":-1,"description":"keratin 128 pseudogene [Source:HGNC Symbol;Acc:HGNC:48882]"}, {"versioned_ensembl_gene_id":"ENSG00000250752.2","gene_symbol":"RPL23AP96","gene_name":"ribosomal protein L23a pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:51631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392181","summary":null,"start":6898878,"end":6899468,"strand":-1,"description":"ribosomal protein L23a pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:51631]"}, {"versioned_ensembl_gene_id":"ENSG00000204909.7","gene_symbol":"SPINK9","gene_name":"serine peptidase inhibitor, Kazal type 9 [Source:HGNC Symbol;Acc:HGNC:32951]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643394","summary":"The protein encoded by this gene is a Kazal-type serine protease inhibitor that appears to specifically target kallikrein-related peptidase 5 (KLK5) in the palmo-plantar epidermis. KLK5 is an important initiator of skin desquamation, so the encoded protease inhibitor may regulate skin differentiation in the palms of hands and soles of feet. This cationic protein has also been shown to promote keratinocyte migration by activation of the epidermal growth factor receptor (EGFR). [provided by RefSeq, Dec 2015]","start":148321203,"end":148339849,"strand":1,"description":"serine peptidase inhibitor, Kazal type 9 [Source:HGNC Symbol;Acc:HGNC:32951]"}, {"versioned_ensembl_gene_id":"ENSG00000072958.8","gene_symbol":"AP1M1","gene_name":"adaptor related protein complex 1 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:13667]","synonyms":"CLAPM2,AP47","biotype":"protein_coding","ncbi_id":"8907","summary":"The protein encoded by this gene is the medium chain of the trans-Golgi network clathrin-associated protein complex AP-1. The other components of this complex are beta-prime-adaptin, gamma-adaptin, and the small chain AP1S1. This complex is located at the Golgi vesicle and links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. Alternatively spliced transcript variants encoding distinct protein isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":16197578,"end":16245907,"strand":1,"description":"adaptor related protein complex 1 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:13667]"}, {"versioned_ensembl_gene_id":"ENSG00000165626.16","gene_symbol":"BEND7","gene_name":"BEN domain containing 7 [Source:HGNC Symbol;Acc:HGNC:23514]","synonyms":"FLJ40283,C10orf30","biotype":"protein_coding","ncbi_id":"222389","summary":null,"start":13438484,"end":13528974,"strand":-1,"description":"BEN domain containing 7 [Source:HGNC Symbol;Acc:HGNC:23514]"}, {"versioned_ensembl_gene_id":"ENSG00000254714.1","gene_symbol":"AP006587.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49850629,"end":49862528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213376.4","gene_symbol":"GAPDHP71","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:4149]","synonyms":"GAPDL16,GAPDHL16","biotype":"processed_pseudogene","ncbi_id":"2613","summary":null,"start":174513305,"end":174514307,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:4149]"}, {"versioned_ensembl_gene_id":"ENSG00000269656.1","gene_symbol":"NOP53-AS1","gene_name":"NOP53 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51587]","synonyms":"GLTSCR2-AS1","biotype":"antisense_RNA","ncbi_id":"106144593","summary":null,"start":47757036,"end":47768840,"strand":-1,"description":"NOP53 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51587]"}, {"versioned_ensembl_gene_id":"ENSG00000198301.11","gene_symbol":"SDAD1","gene_name":"SDA1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25537]","synonyms":"FLJ10498","biotype":"protein_coding","ncbi_id":"55153","summary":null,"start":75940950,"end":75990962,"strand":-1,"description":"SDA1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25537]"}, {"versioned_ensembl_gene_id":"ENSG00000250982.2","gene_symbol":"GAPDHP35","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:37789]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647001","summary":null,"start":28239693,"end":28240668,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:37789]"}, {"versioned_ensembl_gene_id":"ENSG00000161270.19","gene_symbol":"NPHS1","gene_name":"NPHS1, nephrin [Source:HGNC Symbol;Acc:HGNC:7908]","synonyms":"NPHN,CNF","biotype":"protein_coding","ncbi_id":"4868","summary":"This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]","start":35825964,"end":35869287,"strand":-1,"description":"NPHS1, nephrin [Source:HGNC Symbol;Acc:HGNC:7908]"}, {"versioned_ensembl_gene_id":"ENSG00000231372.8","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31545102,"end":31550607,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000239998.5","gene_symbol":"LILRA2","gene_name":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]","synonyms":"LIR7,LIR-7,ILT1,CD85h","biotype":"protein_coding","ncbi_id":"11027","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]","start":54572920,"end":54590287,"strand":1,"description":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]"}, {"versioned_ensembl_gene_id":"ENSG00000241879.1","gene_symbol":"KLF3P2","gene_name":"Kruppel like factor 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41519]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100124394","summary":null,"start":156977558,"end":156977825,"strand":1,"description":"Kruppel like factor 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41519]"}, {"versioned_ensembl_gene_id":"ENSG00000140650.11","gene_symbol":"PMM2","gene_name":"phosphomannomutase 2 [Source:HGNC Symbol;Acc:HGNC:9115]","synonyms":"PMI1,PMI,CDGS,CDG1a,CDG1","biotype":"protein_coding","ncbi_id":"5373","summary":"The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I. [provided by RefSeq, Jul 2008]","start":8788823,"end":8849331,"strand":1,"description":"phosphomannomutase 2 [Source:HGNC Symbol;Acc:HGNC:9115]"}, {"versioned_ensembl_gene_id":"ENSG00000145198.14","gene_symbol":"VWA5B2","gene_name":"von Willebrand factor A domain containing 5B2 [Source:HGNC Symbol;Acc:HGNC:25144]","synonyms":"LOC90113,DKFZp761K032","biotype":"protein_coding","ncbi_id":"90113","summary":null,"start":184230429,"end":184242329,"strand":1,"description":"von Willebrand factor A domain containing 5B2 [Source:HGNC Symbol;Acc:HGNC:25144]"}, {"versioned_ensembl_gene_id":"ENSG00000103064.13","gene_symbol":"SLC7A6","gene_name":"solute carrier family 7 member 6 [Source:HGNC Symbol;Acc:HGNC:11064]","synonyms":"y+LAT-2,LAT3,LAT-2,KIAA0245","biotype":"protein_coding","ncbi_id":"9057","summary":null,"start":68264516,"end":68301823,"strand":1,"description":"solute carrier family 7 member 6 [Source:HGNC Symbol;Acc:HGNC:11064]"}, {"versioned_ensembl_gene_id":"ENSG00000232339.5","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32234228,"end":32263476,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000239861.1","gene_symbol":"AP001486.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103045237,"end":103045712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282849.1","gene_symbol":"AL359834.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":200478020,"end":200483604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128891.15","gene_symbol":"CCDC32","gene_name":"coiled-coil domain containing 32 [Source:HGNC Symbol;Acc:HGNC:28295]","synonyms":"C15orf57,MGC20481","biotype":"protein_coding","ncbi_id":"90416","summary":null,"start":40528683,"end":40565057,"strand":-1,"description":"coiled-coil domain containing 32 [Source:HGNC Symbol;Acc:HGNC:28295]"}, {"versioned_ensembl_gene_id":"ENSG00000253652.1","gene_symbol":"AC136628.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179503322,"end":179515579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205625.2","gene_symbol":"AL591499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154706643,"end":154707795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231316.1","gene_symbol":"AL591419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154605616,"end":154605954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196440.11","gene_symbol":"ARMCX4","gene_name":"armadillo repeat containing, X-linked 4 [Source:HGNC Symbol;Acc:HGNC:28615]","synonyms":"MGC40053,GASP4,CXorf35","biotype":"protein_coding","ncbi_id":"100131755","summary":"The product of this gene belongs to the armadillo repeat-containing family of proteins, which interact with other proteins in a variety of cellular processes. The function of this family member is currently unknown. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":101418287,"end":101533459,"strand":1,"description":"armadillo repeat containing, X-linked 4 [Source:HGNC Symbol;Acc:HGNC:28615]"}, {"versioned_ensembl_gene_id":"ENSG00000225889.7","gene_symbol":"AC012368.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64143239,"end":64252859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283897.1","gene_symbol":"AC011416.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127215159,"end":127229809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223489.1","gene_symbol":"NEFHP1","gene_name":"neurofilament heavy pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7738]","synonyms":"NEFHL","biotype":"processed_pseudogene","ncbi_id":"339396","summary":null,"start":116739981,"end":116742609,"strand":-1,"description":"neurofilament heavy pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7738]"}, {"versioned_ensembl_gene_id":"ENSG00000254935.1","gene_symbol":"AP002469.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122618851,"end":122619274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196141.13","gene_symbol":"SPATS2L","gene_name":"spermatogenesis associated serine rich 2 like [Source:HGNC Symbol;Acc:HGNC:24574]","synonyms":"SGNP,DNAPTP6","biotype":"protein_coding","ncbi_id":"26010","summary":null,"start":200305881,"end":200482263,"strand":1,"description":"spermatogenesis associated serine rich 2 like [Source:HGNC Symbol;Acc:HGNC:24574]"}, {"versioned_ensembl_gene_id":"ENSG00000095370.19","gene_symbol":"SH2D3C","gene_name":"SH2 domain containing 3C [Source:HGNC Symbol;Acc:HGNC:16884]","synonyms":"NSP3","biotype":"protein_coding","ncbi_id":"10044","summary":"This gene encodes an adaptor protein and member of a cytoplasmic protein family involved in cell migration. The encoded protein contains a putative Src homology 2 (SH2) domain and guanine nucleotide exchange factor-like domain which allows this signaling protein to form a complex with scaffolding protein Crk-associated substrate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":127738317,"end":127778741,"strand":-1,"description":"SH2 domain containing 3C [Source:HGNC Symbol;Acc:HGNC:16884]"}, {"versioned_ensembl_gene_id":"ENSG00000275310.1","gene_symbol":"AC006158.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9325799,"end":9326047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143228.12","gene_symbol":"NUF2","gene_name":"NUF2, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:14621]","synonyms":"NUF2R,CT106,CDCA1","biotype":"protein_coding","ncbi_id":"83540","summary":"This gene encodes a protein that is highly similar to yeast Nuf2, a component of a conserved protein complex associated with the centromere. Yeast Nuf2 disappears from the centromere during meiotic prophase when centromeres lose their connection to the spindle pole body, and plays a regulatory role in chromosome segregation. The encoded protein is found to be associated with centromeres of mitotic HeLa cells, which suggests that this protein is a functional homolog of yeast Nuf2. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]","start":163266576,"end":163355764,"strand":1,"description":"NUF2, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:14621]"}, {"versioned_ensembl_gene_id":"ENSG00000240180.1","gene_symbol":"RPL12P28","gene_name":"ribosomal protein L12 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271273","summary":null,"start":5861805,"end":5862594,"strand":-1,"description":"ribosomal protein L12 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36818]"}, {"versioned_ensembl_gene_id":"ENSG00000226964.1","gene_symbol":"RHEBP2","gene_name":"Ras-homolog enriched in brain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44991]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060032","summary":null,"start":47706203,"end":47706802,"strand":1,"description":"Ras-homolog enriched in brain pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44991]"}, {"versioned_ensembl_gene_id":"ENSG00000105058.11","gene_symbol":"FAM32A","gene_name":"family with sequence similarity 32 member A [Source:HGNC Symbol;Acc:HGNC:24563]","synonyms":"OTAG-12,DKFZP586O0120","biotype":"protein_coding","ncbi_id":"26017","summary":null,"start":16185380,"end":16192046,"strand":1,"description":"family with sequence similarity 32 member A [Source:HGNC Symbol;Acc:HGNC:24563]"}, {"versioned_ensembl_gene_id":"ENSG00000233251.7","gene_symbol":"AC007743.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56173534,"end":56185770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228798.1","gene_symbol":"AP000473.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16630827,"end":16640683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280305.1","gene_symbol":"AC018765.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29979669,"end":29983114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136021.18","gene_symbol":"SCYL2","gene_name":"SCY1 like pseudokinase 2 [Source:HGNC Symbol;Acc:HGNC:19286]","synonyms":"KIAA1360,CVAK104","biotype":"protein_coding","ncbi_id":"55681","summary":"The protein encoded by this gene associates with clathrin-coated complexes at the plasma membrane and with endocytic coated vesicles. The encoded protein phosphorylates the beta2 subunit of the plasma membrane adapter complex AP2 and interacts with clathrin, showing involvement in clathrin-dependent pathways between the trans-Golgi network and the endosomal system. In addition, this protein has a role in the Wnt signaling pathway by targeting frizzled 5 (Fzd5) for lysosomal degradation. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015]","start":100267140,"end":100341724,"strand":1,"description":"SCY1 like pseudokinase 2 [Source:HGNC Symbol;Acc:HGNC:19286]"}, {"versioned_ensembl_gene_id":"ENSG00000248511.1","gene_symbol":"AC112695.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92297251,"end":92304178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233787.3","gene_symbol":"AC010374.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29881709,"end":29882945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237499.6","gene_symbol":"AL357060.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137823673,"end":137868233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226742.3","gene_symbol":"HSBP1L1","gene_name":"heat shock factor binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:37243]","synonyms":"MGC189743,FLJ10967","biotype":"protein_coding","ncbi_id":"440498","summary":null,"start":79964561,"end":79970822,"strand":1,"description":"heat shock factor binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:37243]"}, {"versioned_ensembl_gene_id":"ENSG00000257729.1","gene_symbol":"AC087798.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84271340,"end":84294562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271204.1","gene_symbol":"AC016831.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130930209,"end":130932206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227647.2","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"HCGIX-4,PERB11,HCGIX,HCGIX4","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29970259,"end":29973553,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000258914.1","gene_symbol":"AL132712.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103875055,"end":103877478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170255.7","gene_symbol":"MRGPRX1","gene_name":"MAS related GPR family member X1 [Source:HGNC Symbol;Acc:HGNC:17962]","synonyms":"MRGX1","biotype":"protein_coding","ncbi_id":"259249","summary":null,"start":18933813,"end":18939507,"strand":-1,"description":"MAS related GPR family member X1 [Source:HGNC Symbol;Acc:HGNC:17962]"}, {"versioned_ensembl_gene_id":"ENSG00000152234.15","gene_symbol":"ATP5A1","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle [Source:HGNC Symbol;Acc:HGNC:823]","synonyms":"ORM,OMR,hATP1,ATPM,ATP5AL2,ATP5A","biotype":"protein_coding","ncbi_id":"498","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, using an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the alpha subunit of the catalytic core. Alternatively spliced transcript variants encoding the different isoforms have been identified. Pseudogenes of this gene are located on chromosomes 9, 2, and 16. [provided by RefSeq, Mar 2012]","start":46080248,"end":46104334,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle [Source:HGNC Symbol;Acc:HGNC:823]"}, {"versioned_ensembl_gene_id":"ENSG00000231926.1","gene_symbol":"SEPHS1P7","gene_name":"selenophosphate synthetase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391428","summary":null,"start":114260050,"end":114261226,"strand":-1,"description":"selenophosphate synthetase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42167]"}, {"versioned_ensembl_gene_id":"ENSG00000113240.12","gene_symbol":"CLK4","gene_name":"CDC like kinase 4 [Source:HGNC Symbol;Acc:HGNC:13659]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57396","summary":"The protein encoded by this gene belongs to the CDC2-like protein kinase (CLK) family. This protein kinase can interact with and phosphorylate the serine- and arginine-rich (SR) proteins, which are known to play an important role in the formation of spliceosomes, and thus may be involved in the regulation of alternative splicing. Studies in the Israeli sand rat Psammomys obesus suggested that the ubiquitin-like 5 (UBL5/BEACON), a highly conserved ubiquitin-like protein, may interact with and regulate the activity of this kinase. Multiple alternatively spliced transcript variants have been observed, but the full-length natures of which have not yet been determined. [provided by RefSeq, Jul 2008]","start":178602664,"end":178630615,"strand":-1,"description":"CDC like kinase 4 [Source:HGNC Symbol;Acc:HGNC:13659]"}, {"versioned_ensembl_gene_id":"ENSG00000259235.1","gene_symbol":"AC066612.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48189037,"end":48191691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240373.1","gene_symbol":"SEC62-AS1","gene_name":"SEC62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40586]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478967","summary":null,"start":169978536,"end":169985715,"strand":-1,"description":"SEC62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40586]"}, {"versioned_ensembl_gene_id":"ENSG00000147403.16","gene_symbol":"RPL10","gene_name":"ribosomal protein L10 [Source:HGNC Symbol;Acc:HGNC:10298]","synonyms":"QM,NOV,L10,FLJ23544,DXS648E,DXS648","biotype":"protein_coding","ncbi_id":"6134","summary":"This gene encodes a ribosomal protein that is a component of the 60S ribosome subunit. The related protein in chicken can bind to c-Jun and can repress c-Jun-mediated transcriptional activation. Some studies have detected an association between variation in this gene and autism spectrum disorders, though others do not detect this relationship. There are multiple pseudogenes of this gene dispersed throughout the genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":154389955,"end":154409168,"strand":1,"description":"ribosomal protein L10 [Source:HGNC Symbol;Acc:HGNC:10298]"}, {"versioned_ensembl_gene_id":"ENSG00000229849.1","gene_symbol":"PYHIN5P","gene_name":"pyrin and HIN domain family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:51820]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646377","summary":null,"start":158878746,"end":158883500,"strand":1,"description":"pyrin and HIN domain family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:51820]"}, {"versioned_ensembl_gene_id":"ENSG00000168384.11","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33098041,"end":33114235,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000237133.1","gene_symbol":"AC020594.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33555047,"end":33563547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254639.1","gene_symbol":"AC116021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46238382,"end":46239267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279957.1","gene_symbol":"AC110769.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":113904086,"end":113905258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229338.1","gene_symbol":"AL136084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98890590,"end":98891937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176994.10","gene_symbol":"SMCR8","gene_name":"Smith-Magenis syndrome chromosome region, candidate 8 [Source:HGNC Symbol;Acc:HGNC:17921]","synonyms":"FLJ34716","biotype":"protein_coding","ncbi_id":"140775","summary":null,"start":18315310,"end":18328055,"strand":1,"description":"Smith-Magenis syndrome chromosome region, candidate 8 [Source:HGNC Symbol;Acc:HGNC:17921]"}, {"versioned_ensembl_gene_id":"ENSG00000226364.1","gene_symbol":"LINC02089","gene_name":"long intergenic non-protein coding RNA 2089 [Source:HGNC Symbol;Acc:HGNC:52940]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371831","summary":null,"start":52862121,"end":52899588,"strand":1,"description":"long intergenic non-protein coding RNA 2089 [Source:HGNC Symbol;Acc:HGNC:52940]"}, {"versioned_ensembl_gene_id":"ENSG00000251079.6","gene_symbol":"BMS1P2","gene_name":"BMS1, ribosome biogenesis factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23650]","synonyms":"OTTHUMG00000018142,OTTHUMG00000018113,BMS1P6,BMS1LP6,BMS1LP2,bA302K17.2,bA144G6.1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":47538377,"end":47551954,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23650]"}, {"versioned_ensembl_gene_id":"ENSG00000197930.12","gene_symbol":"ERO1A","gene_name":"endoplasmic reticulum oxidoreductase 1 alpha [Source:HGNC Symbol;Acc:HGNC:13280]","synonyms":"ERO1L,Ero1alpha,ERO1-alpha","biotype":"protein_coding","ncbi_id":"30001","summary":null,"start":52639916,"end":52695900,"strand":-1,"description":"endoplasmic reticulum oxidoreductase 1 alpha [Source:HGNC Symbol;Acc:HGNC:13280]"}, {"versioned_ensembl_gene_id":"ENSG00000162460.6","gene_symbol":"TMEM82","gene_name":"transmembrane protein 82 [Source:HGNC Symbol;Acc:HGNC:32350]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388595","summary":null,"start":15742422,"end":15747982,"strand":1,"description":"transmembrane protein 82 [Source:HGNC Symbol;Acc:HGNC:32350]"}, {"versioned_ensembl_gene_id":"ENSG00000255219.1","gene_symbol":"AP000755.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122295190,"end":122308019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248124.7","gene_symbol":"RRN3P1","gene_name":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30548]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"730092","summary":null,"start":21796106,"end":21820410,"strand":-1,"description":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30548]"}, {"versioned_ensembl_gene_id":"ENSG00000255015.1","gene_symbol":"AP000755.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122294938,"end":122301763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234964.4","gene_symbol":"FABP5P7","gene_name":"fatty acid binding protein 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31070]","synonyms":"FABP5L7","biotype":"processed_pseudogene","ncbi_id":"728641","summary":null,"start":59781318,"end":59781722,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31070]"}, {"versioned_ensembl_gene_id":"ENSG00000233858.4","gene_symbol":"AC026904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48590401,"end":48594621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225521.1","gene_symbol":"AC005237.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241015599,"end":241064116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262406.2","gene_symbol":"MMP12","gene_name":"matrix metallopeptidase 12 [Source:HGNC Symbol;Acc:HGNC:7158]","synonyms":"HME","biotype":"protein_coding","ncbi_id":"4321","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This protease degrades soluble and insoluble elastin. This gene may play a role in aneurysm formation and mutations in this gene are associated with lung function and chronic obstructive pulmonary disease (COPD). This gene is part of a cluster of MMP genes on chromosome 11. [provided by RefSeq, Jan 2016]","start":102862736,"end":102875034,"strand":-1,"description":"matrix metallopeptidase 12 [Source:HGNC Symbol;Acc:HGNC:7158]"}, {"versioned_ensembl_gene_id":"ENSG00000268746.1","gene_symbol":"AC010519.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47607524,"end":47733098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275045.4","gene_symbol":"GTF2H2","gene_name":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]","synonyms":"TFIIH,T-BTF2P44,p44,BTF2P44,BTF2","biotype":"protein_coding","ncbi_id":"2966","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq, Jul 2008]","start":69559974,"end":69592641,"strand":1,"description":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]"}, {"versioned_ensembl_gene_id":"ENSG00000269495.1","gene_symbol":"AC011483.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50950185,"end":50963649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130649.9","gene_symbol":"CYP2E1","gene_name":"cytochrome P450 family 2 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:2631]","synonyms":"CYP2E","biotype":"protein_coding","ncbi_id":"1571","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is induced by ethanol, the diabetic state, and starvation. The enzyme metabolizes both endogenous substrates, such as ethanol, acetone, and acetal, as well as exogenous substrates including benzene, carbon tetrachloride, ethylene glycol, and nitrosamines which are premutagens found in cigarette smoke. Due to its many substrates, this enzyme may be involved in such varied processes as gluconeogenesis, hepatic cirrhosis, diabetes, and cancer. [provided by RefSeq, Jul 2008]","start":133520406,"end":133561220,"strand":1,"description":"cytochrome P450 family 2 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:2631]"}, {"versioned_ensembl_gene_id":"ENSG00000067365.14","gene_symbol":"METTL22","gene_name":"methyltransferase like 22 [Source:HGNC Symbol;Acc:HGNC:28368]","synonyms":"FLJ12433,C16orf68,MGC2654","biotype":"protein_coding","ncbi_id":"79091","summary":"This gene encodes a member of the non-histone lysine methyltransferases. It interacts with its substrate, Kin17, which is involved in DNA repair and replication and mRNA processing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":8621683,"end":8649654,"strand":1,"description":"methyltransferase like 22 [Source:HGNC Symbol;Acc:HGNC:28368]"}, {"versioned_ensembl_gene_id":"ENSG00000265287.2","gene_symbol":"AC005726.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28607963,"end":28609730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102125.15","gene_symbol":"TAZ","gene_name":"tafazzin [Source:HGNC Symbol;Acc:HGNC:11577]","synonyms":"XAP-2,TAZ1,G4.5,EFE2,EFE,CMD3A,BTHS","biotype":"protein_coding","ncbi_id":"6901","summary":"This gene encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in this gene have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is produced; the short form lacks a hydrophobic leader sequence and may exist as a cytoplasmic protein rather than being membrane-bound. Other alternatively spliced transcripts have been described but the full-length nature of all these transcripts is not known. [provided by RefSeq, Jul 2008]","start":154411518,"end":154421726,"strand":1,"description":"tafazzin [Source:HGNC Symbol;Acc:HGNC:11577]"}, {"versioned_ensembl_gene_id":"ENSG00000235956.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32156028,"end":32162042,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000213590.2","gene_symbol":"AL807752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136935840,"end":136937161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188784.4","gene_symbol":"PLA2G2E","gene_name":"phospholipase A2 group IIE [Source:HGNC Symbol;Acc:HGNC:13414]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30814","summary":null,"start":19920009,"end":19923617,"strand":-1,"description":"phospholipase A2 group IIE [Source:HGNC Symbol;Acc:HGNC:13414]"}, {"versioned_ensembl_gene_id":"ENSG00000273025.1","gene_symbol":"AC009690.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":72266746,"end":72319946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274497.2","gene_symbol":"IGHG2","gene_name":"immunoglobulin heavy constant gamma 2 (G2m marker) [Source:HGNC Symbol;Acc:HGNC:5526]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3501","summary":null,"start":105643841,"end":105645561,"strand":-1,"description":"immunoglobulin heavy constant gamma 2 (G2m marker) [Source:HGNC Symbol;Acc:HGNC:5526]"}, {"versioned_ensembl_gene_id":"ENSG00000257262.1","gene_symbol":"AC023511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30200983,"end":30217916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257756.5","gene_symbol":"LINC02386","gene_name":"long intergenic non-protein coding RNA 2386 [Source:HGNC Symbol;Acc:HGNC:53312]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369717","summary":null,"start":30230779,"end":30296707,"strand":-1,"description":"long intergenic non-protein coding RNA 2386 [Source:HGNC Symbol;Acc:HGNC:53312]"}, {"versioned_ensembl_gene_id":"ENSG00000127191.17","gene_symbol":"TRAF2","gene_name":"TNF receptor associated factor 2 [Source:HGNC Symbol;Acc:HGNC:12032]","synonyms":"TRAP3","biotype":"protein_coding","ncbi_id":"7186","summary":"The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from members of the TNF receptor superfamily. This protein directly interacts with TNF receptors, and forms a heterodimeric complex with TRAF1. This protein is required for TNF-alpha-mediated activation of MAPK8/JNK and NF-kappaB. The protein complex formed by this protein and TRAF1 interacts with the inhibitor-of-apoptosis proteins (IAPs), and functions as a mediator of the anti-apoptotic signals from TNF receptors. The interaction of this protein with TRADD, a TNF receptor associated apoptotic signal transducer, ensures the recruitment of IAPs for the direct inhibition of caspase activation. BIRC2/c-IAP1, an apoptosis inhibitor possessing ubiquitin ligase activity, can unbiquitinate and induce the degradation of this protein, and thus potentiate TNF-induced apoptosis. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of only one transcript has been determined. [provided by RefSeq, Jul 2008]","start":136881912,"end":136926607,"strand":1,"description":"TNF receptor associated factor 2 [Source:HGNC Symbol;Acc:HGNC:12032]"}, {"versioned_ensembl_gene_id":"ENSG00000184224.3","gene_symbol":"C11orf72","gene_name":"chromosome 11 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:26915]","synonyms":"FLJ90834","biotype":"lincRNA","ncbi_id":"100505621","summary":null,"start":67602880,"end":67606706,"strand":-1,"description":"chromosome 11 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:26915]"}, {"versioned_ensembl_gene_id":"ENSG00000107249.21","gene_symbol":"GLIS3","gene_name":"GLIS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:28510]","synonyms":"ZNF515,MGC33662","biotype":"protein_coding","ncbi_id":"169792","summary":"This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear protein with five C2H2-type zinc finger domains. This protein functions as both a repressor and activator of transcription and is specifically involved in the development of pancreatic beta cells, the thyroid, eye, liver and kidney. Mutations in this gene have been associated with neonatal diabetes and congenital hypothyroidism (NDH). Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only two have been determined. [provided by RefSeq, Jul 2008]","start":3824127,"end":4348392,"strand":-1,"description":"GLIS family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:28510]"}, {"versioned_ensembl_gene_id":"ENSG00000110955.8","gene_symbol":"ATP5B","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide [Source:HGNC Symbol;Acc:HGNC:830]","synonyms":"ATPSB","biotype":"protein_coding","ncbi_id":"506","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the beta subunit of the catalytic core. [provided by RefSeq, Jul 2008]","start":56638175,"end":56646068,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide [Source:HGNC Symbol;Acc:HGNC:830]"}, {"versioned_ensembl_gene_id":"ENSG00000249658.1","gene_symbol":"AC005823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51335261,"end":51336240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225860.2","gene_symbol":"LINC02072","gene_name":"long intergenic non-protein coding RNA 2072 [Source:HGNC Symbol;Acc:HGNC:52918]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440446","summary":null,"start":51336715,"end":51342571,"strand":1,"description":"long intergenic non-protein coding RNA 2072 [Source:HGNC Symbol;Acc:HGNC:52918]"}, {"versioned_ensembl_gene_id":"ENSG00000258502.5","gene_symbol":"LINC02290","gene_name":"long intergenic non-protein coding RNA 2290 [Source:HGNC Symbol;Acc:HGNC:53206]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370540","summary":null,"start":66111581,"end":66125847,"strand":1,"description":"long intergenic non-protein coding RNA 2290 [Source:HGNC Symbol;Acc:HGNC:53206]"}, {"versioned_ensembl_gene_id":"ENSG00000163563.7","gene_symbol":"MNDA","gene_name":"myeloid cell nuclear differentiation antigen [Source:HGNC Symbol;Acc:HGNC:7183]","synonyms":"PYHIN3","biotype":"protein_coding","ncbi_id":"4332","summary":"The myeloid cell nuclear differentiation antigen (MNDA) is detected only in nuclei of cells of the granulocyte-monocyte lineage. A 200-amino acid region of human MNDA is strikingly similar to a region in the proteins encoded by a family of interferon-inducible mouse genes, designated Ifi-201, Ifi-202, and Ifi-203, that are not regulated in a cell- or tissue-specific fashion. The 1.8-kb MNDA mRNA, which contains an interferon-stimulated response element in the 5-prime untranslated region, was significantly upregulated in human monocytes exposed to interferon alpha. MNDA is located within 2,200 kb of FCER1A, APCS, CRP, and SPTA1. In its pattern of expression and/or regulation, MNDA resembles IFI16, suggesting that these genes participate in blood cell-specific responses to interferons. [provided by RefSeq, Jul 2008]","start":158831317,"end":158849506,"strand":1,"description":"myeloid cell nuclear differentiation antigen [Source:HGNC Symbol;Acc:HGNC:7183]"}, {"versioned_ensembl_gene_id":"ENSG00000105429.12","gene_symbol":"MEGF8","gene_name":"multiple EGF like domains 8 [Source:HGNC Symbol;Acc:HGNC:3233]","synonyms":"EGFL4,C19orf49,SBP1,FLJ22365","biotype":"protein_coding","ncbi_id":"1954","summary":"The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":42325609,"end":42378769,"strand":1,"description":"multiple EGF like domains 8 [Source:HGNC Symbol;Acc:HGNC:3233]"}, {"versioned_ensembl_gene_id":"ENSG00000180433.5","gene_symbol":"OR6K6","gene_name":"olfactory receptor family 6 subfamily K member 6 [Source:HGNC Symbol;Acc:HGNC:15033]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128371","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158754720,"end":158755891,"strand":1,"description":"olfactory receptor family 6 subfamily K member 6 [Source:HGNC Symbol;Acc:HGNC:15033]"}, {"versioned_ensembl_gene_id":"ENSG00000251688.1","gene_symbol":"LINC02507","gene_name":"long intergenic non-protein coding RNA 2507 [Source:HGNC Symbol;Acc:HGNC:53496]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377477","summary":null,"start":147567606,"end":147594587,"strand":1,"description":"long intergenic non-protein coding RNA 2507 [Source:HGNC Symbol;Acc:HGNC:53496]"}, {"versioned_ensembl_gene_id":"ENSG00000274964.1","gene_symbol":"AC026356.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32339368,"end":32340724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257094.1","gene_symbol":"AC016957.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32007127,"end":32007435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172215.5","gene_symbol":"CXCR6","gene_name":"C-X-C motif chemokine receptor 6 [Source:HGNC Symbol;Acc:HGNC:16647]","synonyms":"TYMSTR,STRL33,CD186,BONZO","biotype":"protein_coding","ncbi_id":"10663","summary":"The protein encoded by this gene is a G protein-coupled receptor with seven transmembrane domains that belongs to the CXC chemokine receptor family. This family also includes CXCR1, CXCR2, CXCR3, CXCR4, CXCR5, and CXCR7. This gene, which maps to the chemokine receptor gene cluster, is expressed in several T lymphocyte subsets and bone marrow stromal cells. The encoded protein and its exclusive ligand, chemokine ligand 16 (CCL16), are part of a signalling pathway that regulates T lymphocyte migration to various peripheral tissues (the liver, spleen red pulp, intestine, lungs, and skin) and promotes cell-cell interaction with dendritic cells and fibroblastic reticular cells. CXCR6/CCL16 also controls the localization of resident memory T lymphocytes to different compartments of the lung and maintains airway resident memory T lymphocytes, which are an important first line of defense against respiratory pathogens. The encoded protein serves as an entry coreceptor used by HIV-1 and SIV to enter target cells, in conjunction with CD4. [provided by RefSeq, Aug 2020]","start":45940933,"end":45948353,"strand":1,"description":"C-X-C motif chemokine receptor 6 [Source:HGNC Symbol;Acc:HGNC:16647]"}, {"versioned_ensembl_gene_id":"ENSG00000213701.4","gene_symbol":"SETP22","gene_name":"SET pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42941]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642737","summary":null,"start":97056402,"end":97057358,"strand":-1,"description":"SET pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42941]"}, {"versioned_ensembl_gene_id":"ENSG00000143499.13","gene_symbol":"SMYD2","gene_name":"SET and MYND domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20982]","synonyms":"ZMYND14,KMT3C,HSKM-B","biotype":"protein_coding","ncbi_id":"56950","summary":"SET domain-containing proteins, such as SMYD2, catalyze lysine methylation (Brown et al., 2006 [PubMed 16805913]).[supplied by OMIM, Nov 2008]","start":214281102,"end":214337131,"strand":1,"description":"SET and MYND domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20982]"}, {"versioned_ensembl_gene_id":"ENSG00000163820.14","gene_symbol":"FYCO1","gene_name":"FYVE and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14673]","synonyms":"ZFYVE7,FLJ13335","biotype":"protein_coding","ncbi_id":"79443","summary":"The gene encodes a Rab7 adapter protein that is implicated in the microtubule transport of autophagosomes. The encoded protein contains a RUN domain, a FYVE-type zinc finger domain, and Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtubule plus end-directed transport of autophagic vesicles through interactions with the small GTPase Rab7, phosphatidylinositol-3-phosphate (PI3P), the autophagosome marker LC3, and the kinesin KIF5. Mutations in this gene are associated with inclusion body myositis (IBM) and autosomal recessive congenital cataracts (CATC2). [provided by RefSeq, Aug 2020]","start":45917899,"end":45995824,"strand":-1,"description":"FYVE and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14673]"}, {"versioned_ensembl_gene_id":"ENSG00000238283.3","gene_symbol":"TBC1D3P1","gene_name":"TBC1 domain family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27445]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400609","summary":null,"start":60008437,"end":60017498,"strand":-1,"description":"TBC1 domain family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27445]"}, {"versioned_ensembl_gene_id":"ENSG00000070756.15","gene_symbol":"PABPC1","gene_name":"poly(A) binding protein cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:8554]","synonyms":"PABPL1,PABPC2,PABP1,PAB1","biotype":"protein_coding","ncbi_id":"26986","summary":"This gene encodes a poly(A) binding protein. The protein shuttles between the nucleus and cytoplasm and binds to the 3' poly(A) tail of eukaryotic messenger RNAs via RNA-recognition motifs. The binding of this protein to poly(A) promotes ribosome recruitment and translation initiation; it is also required for poly(A) shortening which is the first step in mRNA decay. The gene is part of a small gene family including three protein-coding genes and several pseudogenes.[provided by RefSeq, Aug 2010]","start":100685816,"end":100722809,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:8554]"}, {"versioned_ensembl_gene_id":"ENSG00000162542.13","gene_symbol":"TMCO4","gene_name":"transmembrane and coiled-coil domains 4 [Source:HGNC Symbol;Acc:HGNC:27393]","synonyms":"DKFZp686C23231","biotype":"protein_coding","ncbi_id":"255104","summary":null,"start":19682213,"end":19799945,"strand":-1,"description":"transmembrane and coiled-coil domains 4 [Source:HGNC Symbol;Acc:HGNC:27393]"}, {"versioned_ensembl_gene_id":"ENSG00000225973.3","gene_symbol":"PIGBOS1","gene_name":"PIGB opposite strand 1 [Source:HGNC Symbol;Acc:HGNC:50696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928527","summary":null,"start":55317184,"end":55319161,"strand":-1,"description":"PIGB opposite strand 1 [Source:HGNC Symbol;Acc:HGNC:50696]"}, {"versioned_ensembl_gene_id":"ENSG00000254870.5","gene_symbol":"ATP6V1G2-DDX39B","gene_name":"ATP6V1G2-DDX39B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532737","summary":"This locus represents naturally occurring read-through transcription between the neighboring ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) and DDX39B (DEAD box polypeptide 39B) genes located in the major histocompatibility complex class III region of chromosome 6. The read-through transcript and is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31530219,"end":31546608,"strand":-1,"description":"ATP6V1G2-DDX39B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41999]"}, {"versioned_ensembl_gene_id":"ENSG00000114650.18","gene_symbol":"SCAP","gene_name":"SREBF chaperone [Source:HGNC Symbol;Acc:HGNC:30634]","synonyms":"KIAA0199","biotype":"protein_coding","ncbi_id":"22937","summary":"This gene encodes a protein with a sterol sensing domain (SSD) and seven WD domains. In the presence of cholesterol, this protein binds to sterol regulatory element binding proteins (SREBPs) and mediates their transport from the ER to the Golgi. The SREBPs are then proteolytically cleaved and regulate sterol biosynthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":47413694,"end":47477126,"strand":-1,"description":"SREBF chaperone [Source:HGNC Symbol;Acc:HGNC:30634]"}, {"versioned_ensembl_gene_id":"ENSG00000250645.1","gene_symbol":"AC010442.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":418703,"end":419109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267402.1","gene_symbol":"TCF4-AS2","gene_name":"TCF4 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51643]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480339","summary":null,"start":55492175,"end":55496392,"strand":1,"description":"TCF4 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51643]"}, {"versioned_ensembl_gene_id":"ENSG00000270264.1","gene_symbol":"AC004686.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59885015,"end":59885552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223692.1","gene_symbol":"DIP2A-IT1","gene_name":"DIP2A intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41430]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100862692","summary":null,"start":46462471,"end":46469306,"strand":1,"description":"DIP2A intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41430]"}, {"versioned_ensembl_gene_id":"ENSG00000177150.12","gene_symbol":"FAM210A","gene_name":"family with sequence similarity 210 member A [Source:HGNC Symbol;Acc:HGNC:28346]","synonyms":"C18orf19,MGC24180,HsT2329","biotype":"protein_coding","ncbi_id":"125228","summary":null,"start":13663347,"end":13726663,"strand":-1,"description":"family with sequence similarity 210 member A [Source:HGNC Symbol;Acc:HGNC:28346]"}, {"versioned_ensembl_gene_id":"ENSG00000124107.5","gene_symbol":"SLPI","gene_name":"secretory leukocyte peptidase inhibitor [Source:HGNC Symbol;Acc:HGNC:11092]","synonyms":"WFDC4,WAP4,HUSI-I,HUSI,BLPI,ALP,ALK1","biotype":"protein_coding","ncbi_id":"6590","summary":"This gene encodes a secreted inhibitor which protects epithelial tissues from serine proteases. It is found in various secretions including seminal plasma, cervical mucus, and bronchial secretions, and has affinity for trypsin, leukocyte elastase, and cathepsin G. Its inhibitory effect contributes to the immune response by protecting epithelial surfaces from attack by endogenous proteolytic enzymes. This antimicrobial protein has antibacterial, antifungal and antiviral activity. [provided by RefSeq, Nov 2014]","start":45252239,"end":45254564,"strand":-1,"description":"secretory leukocyte peptidase inhibitor [Source:HGNC Symbol;Acc:HGNC:11092]"}, {"versioned_ensembl_gene_id":"ENSG00000198380.12","gene_symbol":"GFPT1","gene_name":"glutamine--fructose-6-phosphate transaminase 1 [Source:HGNC Symbol;Acc:HGNC:4241]","synonyms":"GFAT1,GFAT,GFA,GFPT","biotype":"protein_coding","ncbi_id":"2673","summary":"This gene encodes the first and rate-limiting enzyme of the hexosamine pathway and controls the flux of glucose into the hexosamine pathway. The product of this gene catalyzes the formation of glucosamine 6-phosphate. [provided by RefSeq, Sep 2008]","start":69319769,"end":69387254,"strand":-1,"description":"glutamine--fructose-6-phosphate transaminase 1 [Source:HGNC Symbol;Acc:HGNC:4241]"}, {"versioned_ensembl_gene_id":"ENSG00000168101.14","gene_symbol":"NUDT16L1","gene_name":"nudix hydrolase 16 like 1 [Source:HGNC Symbol;Acc:HGNC:28154]","synonyms":"SDOS","biotype":"protein_coding","ncbi_id":"84309","summary":null,"start":4693694,"end":4695859,"strand":1,"description":"nudix hydrolase 16 like 1 [Source:HGNC Symbol;Acc:HGNC:28154]"}, {"versioned_ensembl_gene_id":"ENSG00000215063.3","gene_symbol":"RPL21P2","gene_name":"ribosomal protein L21 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16539]","synonyms":"bA352D3.1","biotype":"processed_pseudogene","ncbi_id":"140715","summary":null,"start":4059633,"end":4060113,"strand":-1,"description":"ribosomal protein L21 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16539]"}, {"versioned_ensembl_gene_id":"ENSG00000272837.1","gene_symbol":"AC009779.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55646195,"end":55646663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177879.15","gene_symbol":"AP3S1","gene_name":"adaptor related protein complex 3 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:2013]","synonyms":"CLAPS3","biotype":"protein_coding","ncbi_id":"1176","summary":"This gene encodes a subunit of the AP3 adaptor complex. This complex functions in the formation of subcellular vesicles budded from the Golgi body. Several related pseudogenes of this gene have been found. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":115841481,"end":115914081,"strand":1,"description":"adaptor related protein complex 3 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:2013]"}, {"versioned_ensembl_gene_id":"ENSG00000235954.6","gene_symbol":"TTC28-AS1","gene_name":"TTC28 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:29336]","synonyms":"TTC28AS,TTC28-AS,KIAA1648","biotype":"processed_transcript","ncbi_id":"284900","summary":null,"start":27919376,"end":28008581,"strand":1,"description":"TTC28 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:29336]"}, {"versioned_ensembl_gene_id":"ENSG00000126733.20","gene_symbol":"DACH2","gene_name":"dachshund family transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:16814]","synonyms":null,"biotype":"protein_coding","ncbi_id":"117154","summary":"This gene is one of two genes which encode a protein similar to the Drosophila protein dachshund, a transcription factor involved in cell fate determination in the eye, limb and genital disc of the fly. The encoded protein contains two characteristic dachshund domains: an N-terminal domain responsible for DNA binding and a C-terminal domain responsible for protein-protein interactions. This gene is located on the X chromosome and is subject to inactivation by DNA methylation. The encoded protein may be involved in regulation of organogenesis and myogenesis, and may play a role in premature ovarian failure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":86148458,"end":86832604,"strand":1,"description":"dachshund family transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:16814]"}, {"versioned_ensembl_gene_id":"ENSG00000234765.1","gene_symbol":"ELL2P3","gene_name":"elongation factor for RNA polymerase II 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533713","summary":null,"start":68289679,"end":68291280,"strand":-1,"description":"elongation factor for RNA polymerase II 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39345]"}, {"versioned_ensembl_gene_id":"ENSG00000151365.2","gene_symbol":"THRSP","gene_name":"thyroid hormone responsive [Source:HGNC Symbol;Acc:HGNC:11800]","synonyms":"THRP,SPOT14,S14,LPGP1,Lpgp","biotype":"protein_coding","ncbi_id":"7069","summary":"The protein encoded by this gene is similar to the gene product of S14, a rat gene whose expression is limited to liver and adipose tissue and is controlled by nutritional and hormonal factors. This gene has been shown to be expressed in liver and adipocytes, particularly in lipomatous modules. It is also found to be expressed in lipogenic breast cancers, which suggests a role in controlling tumor lipid metabolism. [provided by RefSeq, Jul 2008]","start":78063861,"end":78068351,"strand":1,"description":"thyroid hormone responsive [Source:HGNC Symbol;Acc:HGNC:11800]"}, {"versioned_ensembl_gene_id":"ENSG00000233606.2","gene_symbol":"OR6C66P","gene_name":"olfactory receptor family 6 subfamily C member 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:31296]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"403283","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55385837,"end":55392964,"strand":1,"description":"olfactory receptor family 6 subfamily C member 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:31296]"}, {"versioned_ensembl_gene_id":"ENSG00000247679.2","gene_symbol":"AC139795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177611253,"end":177619754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276342.4","gene_symbol":"TMEM179","gene_name":"transmembrane protein 179 [Source:HGNC Symbol;Acc:HGNC:20137]","synonyms":"C14orf90,TMEM179A,FLJ42486","biotype":"protein_coding","ncbi_id":"388021","summary":null,"start":104474682,"end":104612791,"strand":-1,"description":"transmembrane protein 179 [Source:HGNC Symbol;Acc:HGNC:20137]"}, {"versioned_ensembl_gene_id":"ENSG00000269950.1","gene_symbol":"AP000962.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16574718,"end":16582637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187726.8","gene_symbol":"DNAJB13","gene_name":"DnaJ heat shock protein family (Hsp40) member B13 [Source:HGNC Symbol;Acc:HGNC:30718]","synonyms":"TSARG6,RSPH16A","biotype":"protein_coding","ncbi_id":"374407","summary":"This gene encodes a member of the heat shock protein 40 co-chaperone family which is produced in large amounts in the testis and is located on the radial spokes of the axoneme in human sperm flagella and other flagellar structures. The encoded protein associates with the sperm annulus, as part of the septin complex, through direct interaction with septin 4, during sperm terminal differentiation. Naturally occurring mutations in this gene are associated with primary ciliary dyskinesia and male infertility. [provided by RefSeq, Apr 2017]","start":73950319,"end":73970366,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B13 [Source:HGNC Symbol;Acc:HGNC:30718]"}, {"versioned_ensembl_gene_id":"ENSG00000163257.10","gene_symbol":"DCAF16","gene_name":"DDB1 and CUL4 associated factor 16 [Source:HGNC Symbol;Acc:HGNC:25987]","synonyms":"FLJ20280,C4orf30","biotype":"protein_coding","ncbi_id":"54876","summary":null,"start":17800655,"end":17810758,"strand":-1,"description":"DDB1 and CUL4 associated factor 16 [Source:HGNC Symbol;Acc:HGNC:25987]"}, {"versioned_ensembl_gene_id":"ENSG00000153902.13","gene_symbol":"LGI4","gene_name":"leucine rich repeat LGI family member 4 [Source:HGNC Symbol;Acc:HGNC:18712]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163175","summary":null,"start":35124513,"end":35142451,"strand":-1,"description":"leucine rich repeat LGI family member 4 [Source:HGNC Symbol;Acc:HGNC:18712]"}, {"versioned_ensembl_gene_id":"ENSG00000270960.1","gene_symbol":"AC106872.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164933086,"end":164933506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259375.1","gene_symbol":"AC087286.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85579046,"end":85580178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259453.1","gene_symbol":"AC087286.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":85701109,"end":85702771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261434.1","gene_symbol":"AC021087.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":195778,"end":196341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083099.10","gene_symbol":"LYRM2","gene_name":"LYR motif containing 2 [Source:HGNC Symbol;Acc:HGNC:25229]","synonyms":"DJ122O8.2","biotype":"protein_coding","ncbi_id":"57226","summary":null,"start":89568144,"end":89638753,"strand":-1,"description":"LYR motif containing 2 [Source:HGNC Symbol;Acc:HGNC:25229]"}, {"versioned_ensembl_gene_id":"ENSG00000112144.15","gene_symbol":"ICK","gene_name":"intestinal cell kinase [Source:HGNC Symbol;Acc:HGNC:21219]","synonyms":"KIAA0936,MRK,MGC46090,LCK2","biotype":"protein_coding","ncbi_id":"22858","summary":"Eukaryotic protein kinases are enzymes that belong to a very extensive family of proteins which share a conserved catalytic core common with both serine/threonine and tyrosine protein kinases. This gene encodes an intestinal serine/threonine kinase harboring a dual phosphorylation site found in mitogen-activating protein (MAP) kinases. The protein localizes to the intestinal crypt region and is thought to be important in intestinal epithelial cell proliferation and differentiation. Alternative splicing has been observed at this locus and two variants, encoding the same isoform, have been identified. [provided by RefSeq, Jul 2008]","start":53001279,"end":53061802,"strand":-1,"description":"intestinal cell kinase [Source:HGNC Symbol;Acc:HGNC:21219]"}, {"versioned_ensembl_gene_id":"ENSG00000048540.14","gene_symbol":"LMO3","gene_name":"LIM domain only 3 [Source:HGNC Symbol;Acc:HGNC:6643]","synonyms":"RBTNL2,DAT1,Rhom-3","biotype":"protein_coding","ncbi_id":"55885","summary":"The protein encoded by this gene belongs to the rhombotin family of cysteine-rich LIM domain oncogenes. This gene is predominantly expressed in the brain. Related family members, LMO1 and LMO2 on chromosome 11, have been reported to be involved in chromosomal translocations in T-cell leukemia. Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":16548373,"end":16610594,"strand":-1,"description":"LIM domain only 3 [Source:HGNC Symbol;Acc:HGNC:6643]"}, {"versioned_ensembl_gene_id":"ENSG00000057608.16","gene_symbol":"GDI2","gene_name":"GDP dissociation inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:4227]","synonyms":"RABGDIB","biotype":"protein_coding","ncbi_id":"2665","summary":"GDP dissociation inhibitors are proteins that regulate the GDP-GTP exchange reaction of members of the rab family, small GTP-binding proteins of the ras superfamily, that are involved in vesicular trafficking of molecules between cellular organelles. GDIs slow the rate of dissociation of GDP from rab proteins and release GDP from membrane-bound rabs. GDI2 is ubiquitously expressed. The GDI2 gene contains many repetitive elements indicating that it may be prone to inversion/deletion rearrangements. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":5765223,"end":5842132,"strand":-1,"description":"GDP dissociation inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:4227]"}, {"versioned_ensembl_gene_id":"ENSG00000270036.1","gene_symbol":"AC027243.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76343642,"end":76344365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145979.17","gene_symbol":"TBC1D7","gene_name":"TBC1 domain family member 7 [Source:HGNC Symbol;Acc:HGNC:21066]","synonyms":"FLJ32666,dJ257A7.3","biotype":"protein_coding","ncbi_id":"51256","summary":"This gene encodes a member of the TBC-domain containing protein family. The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation. Mutations in this gene have been associated with autosomal recessive megalencephaly. Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between this locus and downstream LOC100130357. [provided by RefSeq, Jan 2016]","start":13266542,"end":13328583,"strand":-1,"description":"TBC1 domain family member 7 [Source:HGNC Symbol;Acc:HGNC:21066]"}, {"versioned_ensembl_gene_id":"ENSG00000187857.4","gene_symbol":"OR6C75","gene_name":"olfactory receptor family 6 subfamily C member 75 [Source:HGNC Symbol;Acc:HGNC:31304]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390323","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55362975,"end":55369279,"strand":1,"description":"olfactory receptor family 6 subfamily C member 75 [Source:HGNC Symbol;Acc:HGNC:31304]"}, {"versioned_ensembl_gene_id":"ENSG00000185920.15","gene_symbol":"PTCH1","gene_name":"patched 1 [Source:HGNC Symbol;Acc:HGNC:9585]","synonyms":"NBCCS,BCNS,PTCH","biotype":"protein_coding","ncbi_id":"5727","summary":"This gene encodes a member of the patched family of proteins and a component of the hedgehog signaling pathway. Hedgehog signaling is important in embryonic development and tumorigenesis. The encoded protein is the receptor for the secreted hedgehog ligands, which include sonic hedgehog, indian hedgehog and desert hedgehog. Following binding by one of the hedgehog ligands, the encoded protein is trafficked away from the primary cilium, relieving inhibition of the G-protein-coupled receptor smoothened, which results in activation of downstream signaling. Mutations of this gene have been associated with basal cell nevus syndrome and holoprosencephaly. [provided by RefSeq, Aug 2017]","start":95442980,"end":95517057,"strand":-1,"description":"patched 1 [Source:HGNC Symbol;Acc:HGNC:9585]"}, {"versioned_ensembl_gene_id":"ENSG00000280219.1","gene_symbol":"AC093908.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":147487971,"end":147496062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151617.15","gene_symbol":"EDNRA","gene_name":"endothelin receptor type A [Source:HGNC Symbol;Acc:HGNC:3179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1909","summary":"This gene encodes the receptor for endothelin-1, a peptide that plays a role in potent and long-lasting vasoconstriction. This receptor associates with guanine-nucleotide-binding (G) proteins, and this coupling activates a phosphatidylinositol-calcium second messenger system. Polymorphisms in this gene have been linked to migraine headache resistance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":147480917,"end":147544954,"strand":1,"description":"endothelin receptor type A [Source:HGNC Symbol;Acc:HGNC:3179]"}, {"versioned_ensembl_gene_id":"ENSG00000230174.1","gene_symbol":"LINC01149","gene_name":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]","synonyms":"XXbac-BPG181B23.4","biotype":"lincRNA","ncbi_id":"101929111","summary":null,"start":31441667,"end":31446973,"strand":1,"description":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]"}, {"versioned_ensembl_gene_id":"ENSG00000267968.1","gene_symbol":"AC011523.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50830530,"end":50851089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136699.19","gene_symbol":"SMPD4","gene_name":"sphingomyelin phosphodiesterase 4 [Source:HGNC Symbol;Acc:HGNC:32949]","synonyms":"NSMASE3,nSMase-3,NET13,KIAA1418,FLJ20756,FLJ20297","biotype":"protein_coding","ncbi_id":"55627","summary":"The protein encoded by this gene is a sphingomyelinase that catalyzes the hydrolysis of membrane sphingomyelin to form phosphorylcholine and ceramide. This gene is activated by DNA damage, cellular stress, and tumor necrosis factor, but it is downregulated by wild-type p53. The encoded protein localizes to the endoplasmic reticulum and Golgi network. [provided by RefSeq, Mar 2017]","start":130151392,"end":130182750,"strand":-1,"description":"sphingomyelin phosphodiesterase 4 [Source:HGNC Symbol;Acc:HGNC:32949]"}, {"versioned_ensembl_gene_id":"ENSG00000170322.14","gene_symbol":"NFRKB","gene_name":"nuclear factor related to kappaB binding protein [Source:HGNC Symbol;Acc:HGNC:7802]","synonyms":"INO80G,DKFZp547B2013","biotype":"protein_coding","ncbi_id":"4798","summary":null,"start":129863636,"end":129895590,"strand":-1,"description":"nuclear factor related to kappaB binding protein [Source:HGNC Symbol;Acc:HGNC:7802]"}, {"versioned_ensembl_gene_id":"ENSG00000261208.1","gene_symbol":"AL365475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52286797,"end":52289268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170161.6","gene_symbol":"AL512625.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62897449,"end":62900104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232894.1","gene_symbol":"MRPS31P2","gene_name":"mitochondrial ribosomal protein S31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39252]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"341757","summary":null,"start":19552571,"end":19570288,"strand":-1,"description":"mitochondrial ribosomal protein S31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39252]"}, {"versioned_ensembl_gene_id":"ENSG00000270813.2","gene_symbol":"AL035422.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101337725,"end":101338289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230318.2","gene_symbol":"XRCC6P3","gene_name":"X-ray repair cross complementing 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45185]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"127086","summary":null,"start":220313945,"end":220315565,"strand":-1,"description":"X-ray repair cross complementing 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45185]"}, {"versioned_ensembl_gene_id":"ENSG00000271361.1","gene_symbol":"AL133351.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3023142,"end":3023772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227794.5","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"KE-3,S18,HKE3,KE3,D6S218E","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33412156,"end":33415676,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000259704.1","gene_symbol":"AC124248.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":90839724,"end":90841378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236604.1","gene_symbol":"LYPLA2P3","gene_name":"lysophospholipase II pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50446]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128790","summary":null,"start":76970322,"end":76971028,"strand":1,"description":"lysophospholipase II pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50446]"}, {"versioned_ensembl_gene_id":"ENSG00000253736.1","gene_symbol":"AC022217.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172762980,"end":172777774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124789.11","gene_symbol":"NUP153","gene_name":"nucleoporin 153 [Source:HGNC Symbol;Acc:HGNC:8062]","synonyms":"HNUP153","biotype":"protein_coding","ncbi_id":"9972","summary":"Nuclear pore complexes regulate the transport of macromolecules between the nucleus and cytoplasm. They are composed of at least 100 different polypeptide subunits, many of which belong to the nucleoporin family. Nucleoporins are glycoproteins found in nuclear pores and contain characteristic pentapeptide XFXFG repeats as well as O-linked N-acetylglucosamine residues oriented towards the cytoplasm. The protein encoded by this gene has three distinct domains: a N-terminal region containing a pore targeting and an RNA-binding domain domain, a central region containing multiple zinc finger motifs, and a C-terminal region containing multiple XFXFG repeats. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":17615035,"end":17706834,"strand":-1,"description":"nucleoporin 153 [Source:HGNC Symbol;Acc:HGNC:8062]"}, {"versioned_ensembl_gene_id":"ENSG00000276583.4","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195720882,"end":195741123,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000205362.11","gene_symbol":"MT1A","gene_name":"metallothionein 1A [Source:HGNC Symbol;Acc:HGNC:7393]","synonyms":"MT1S,MT1","biotype":"protein_coding","ncbi_id":"4489","summary":"This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions. The conserved cysteine residues co-ordinate metal ions using mercaptide linkages. These proteins act as anti-oxidants, protect against hydroxyl free radicals, are important in homeostatic control of metal in the cell, and play a role in detoxification of heavy metals. Disruption of two metallothionein genes in mouse resulted in defects in protection against heavy metals, oxidative stress, immune reactions, carcinogens, and displayed obesity. [provided by RefSeq, Sep 2017]","start":56638666,"end":56640087,"strand":1,"description":"metallothionein 1A [Source:HGNC Symbol;Acc:HGNC:7393]"}, {"versioned_ensembl_gene_id":"ENSG00000228842.3","gene_symbol":"PCDH9-AS2","gene_name":"PCDH9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39896]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874064","summary":null,"start":66825169,"end":66915031,"strand":1,"description":"PCDH9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39896]"}, {"versioned_ensembl_gene_id":"ENSG00000165841.9","gene_symbol":"CYP2C19","gene_name":"cytochrome P450 family 2 subfamily C member 19 [Source:HGNC Symbol;Acc:HGNC:2621]","synonyms":"P450IIC19,CYP2C,CPCJ","biotype":"protein_coding","ncbi_id":"1557","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize many xenobiotics, including the anticonvulsive drug mephenytoin, omeprazole, diazepam and some barbiturates. Polymorphism within this gene is associated with variable ability to metabolize mephenytoin, known as the poor metabolizer and extensive metabolizer phenotypes. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. [provided by RefSeq, Jul 2008]","start":94762624,"end":94853260,"strand":1,"description":"cytochrome P450 family 2 subfamily C member 19 [Source:HGNC Symbol;Acc:HGNC:2621]"}, {"versioned_ensembl_gene_id":"ENSG00000236872.1","gene_symbol":"AL451136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45415020,"end":45415344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223958.1","gene_symbol":"AC244505.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52707602,"end":52709933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253445.1","gene_symbol":"AC027309.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172690454,"end":172697720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253683.1","gene_symbol":"AC027309.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172656522,"end":172656713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254299.1","gene_symbol":"LINC01944","gene_name":"long intergenic non-protein coding RNA 1944 [Source:HGNC Symbol;Acc:HGNC:52768]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377728","summary":null,"start":172557392,"end":172559014,"strand":-1,"description":"long intergenic non-protein coding RNA 1944 [Source:HGNC Symbol;Acc:HGNC:52768]"}, {"versioned_ensembl_gene_id":"ENSG00000280388.1","gene_symbol":"AC006330.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76043977,"end":76045963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218965.1","gene_symbol":"NACAP7","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49494]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101059973","summary":null,"start":89422099,"end":89423048,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49494]"}, {"versioned_ensembl_gene_id":"ENSG00000236384.7","gene_symbol":"LINC00479","gene_name":"long intergenic non-protein coding RNA 479 [Source:HGNC Symbol;Acc:HGNC:19727]","synonyms":"PRED76,FLJ32835,C21orf129","biotype":"lincRNA","ncbi_id":"150135","summary":null,"start":41711520,"end":41715775,"strand":-1,"description":"long intergenic non-protein coding RNA 479 [Source:HGNC Symbol;Acc:HGNC:19727]"}, {"versioned_ensembl_gene_id":"ENSG00000230995.7","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"FB19,PNUTS,CAT53,p99","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30590243,"end":30608455,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000233397.1","gene_symbol":"AC008063.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162093429,"end":162094854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250485.1","gene_symbol":"EXOC7P1","gene_name":"exocyst complex component 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43871]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391681","summary":null,"start":108417705,"end":108419763,"strand":-1,"description":"exocyst complex component 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43871]"}, {"versioned_ensembl_gene_id":"ENSG00000115661.13","gene_symbol":"STK16","gene_name":"serine/threonine kinase 16 [Source:HGNC Symbol;Acc:HGNC:11394]","synonyms":"PKL12,MPSK","biotype":"protein_coding","ncbi_id":"8576","summary":null,"start":219245455,"end":219250337,"strand":1,"description":"serine/threonine kinase 16 [Source:HGNC Symbol;Acc:HGNC:11394]"}, {"versioned_ensembl_gene_id":"ENSG00000233335.1","gene_symbol":"AC016696.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46256860,"end":46257177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101542.9","gene_symbol":"CDH20","gene_name":"cadherin 20 [Source:HGNC Symbol;Acc:HGNC:1760]","synonyms":"CDH7L3,Cdh7","biotype":"protein_coding","ncbi_id":"28316","summary":"This gene is a type II classical cadherin from the cadherin superfamily and one of three cadherin 7-like genes located in a cluster on chromosome 18. The encoded membrane protein is a calcium dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. Since disturbance of intracellular adhesion is a prerequisite for invasion and metastasis of tumor cells, cadherins are considered prime candidates for tumor suppressor genes. [provided by RefSeq, Jul 2008]","start":61333582,"end":61555773,"strand":1,"description":"cadherin 20 [Source:HGNC Symbol;Acc:HGNC:1760]"}, {"versioned_ensembl_gene_id":"ENSG00000154007.6","gene_symbol":"ASB17","gene_name":"ankyrin repeat and SOCS box containing 17 [Source:HGNC Symbol;Acc:HGNC:19769]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127247","summary":null,"start":75918873,"end":75932431,"strand":-1,"description":"ankyrin repeat and SOCS box containing 17 [Source:HGNC Symbol;Acc:HGNC:19769]"}, {"versioned_ensembl_gene_id":"ENSG00000260832.1","gene_symbol":"AC125793.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82953230,"end":82990298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217488.2","gene_symbol":"AL356057.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":75610958,"end":75611945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140398.13","gene_symbol":"NEIL1","gene_name":"nei like DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:18448]","synonyms":"NEI1,hFPG1,FPG1,FLJ22402","biotype":"protein_coding","ncbi_id":"79661","summary":"This gene is a member of the Nei endonuclease VIII-like gene family which encodes DNA glycosylases. The encoded enzyme participates in the DNA repair pathway by initiating base excision repair by removing damaged bases, primarily oxidized pyrimidines. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":75346955,"end":75357114,"strand":1,"description":"nei like DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:18448]"}, {"versioned_ensembl_gene_id":"ENSG00000104361.9","gene_symbol":"NIPAL2","gene_name":"NIPA like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25854]","synonyms":"NPAL2,FLJ13955","biotype":"protein_coding","ncbi_id":"79815","summary":null,"start":98189833,"end":98294393,"strand":-1,"description":"NIPA like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25854]"}, {"versioned_ensembl_gene_id":"ENSG00000214204.4","gene_symbol":"HNRNPA1P43","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:48772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400769","summary":null,"start":115856910,"end":115857819,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:48772]"}, {"versioned_ensembl_gene_id":"ENSG00000239589.5","gene_symbol":"LINC00879","gene_name":"long intergenic non-protein coding RNA 879 [Source:HGNC Symbol;Acc:HGNC:48566]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255025","summary":null,"start":94938172,"end":95152509,"strand":1,"description":"long intergenic non-protein coding RNA 879 [Source:HGNC Symbol;Acc:HGNC:48566]"}, {"versioned_ensembl_gene_id":"ENSG00000234980.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31330914,"end":31332365,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000170776.21","gene_symbol":"AKAP13","gene_name":"A-kinase anchoring protein 13 [Source:HGNC Symbol;Acc:HGNC:371]","synonyms":"PROTO-LB,LBC,Ht31,HA-3,c-lbc,BRX,ARHGEF13,AKAP-Lbc","biotype":"protein_coding","ncbi_id":"11214","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c-terminal dbl oncogene homology (DH) and pleckstrin homology (PH) domains. The DH domain is associated with guanine nucleotide exchange activation for the Rho/Rac family of small GTP binding proteins, resulting in the conversion of the inactive GTPase to the active form capable of transducing signals. The PH domain has multiple functions. Therefore, these isoforms function as scaffolding proteins to coordinate a Rho signaling pathway, function as protein kinase A-anchoring proteins and, in addition, enhance ligand-dependent activity of estrogen receptors alpha and beta. [provided by RefSeq, Jul 2012]","start":85380571,"end":85749358,"strand":1,"description":"A-kinase anchoring protein 13 [Source:HGNC Symbol;Acc:HGNC:371]"}, {"versioned_ensembl_gene_id":"ENSG00000235382.1","gene_symbol":"MTND4P31","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42218]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873252","summary":null,"start":70124972,"end":70129071,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42218]"}, {"versioned_ensembl_gene_id":"ENSG00000154162.14","gene_symbol":"CDH12","gene_name":"cadherin 12 [Source:HGNC Symbol;Acc:HGNC:1751]","synonyms":"CDHB,Br-cadherin","biotype":"protein_coding","ncbi_id":"1010","summary":"This gene encodes a type II classical cadherin of the cadherin superfamily. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature cadherin protein. These integral membrane proteins mediate calcium-dependent cell-cell adhesion and are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. Type II (atypical) cadherins are defined based on their lack of a histidine-alanine-valine (HAV) cell adhesion recognition sequence specific to type I cadherins. This particular cadherin appears to be expressed specifically in the brain and its temporal pattern of expression would be consistent with a role during a critical period of neuronal development, perhaps specifically during synaptogenesis. [provided by RefSeq, Nov 2015]","start":21750673,"end":22853622,"strand":-1,"description":"cadherin 12 [Source:HGNC Symbol;Acc:HGNC:1751]"}, {"versioned_ensembl_gene_id":"ENSG00000225619.1","gene_symbol":"MYT1L-AS1","gene_name":"MYT1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49274]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"730811","summary":null,"start":2319232,"end":2327110,"strand":1,"description":"MYT1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49274]"}, {"versioned_ensembl_gene_id":"ENSG00000259301.2","gene_symbol":"AC084759.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53837271,"end":53837560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237382.2","gene_symbol":"AC127537.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18312760,"end":18313533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228069.1","gene_symbol":"MTCO3P29","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52132]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075185","summary":null,"start":92109013,"end":92110095,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52132]"}, {"versioned_ensembl_gene_id":"ENSG00000283496.1","gene_symbol":"AL360181.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":133309410,"end":133352529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000002549.12","gene_symbol":"LAP3","gene_name":"leucine aminopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:18449]","synonyms":"PEPS,LAPEP,LAP","biotype":"protein_coding","ncbi_id":"51056","summary":null,"start":17577192,"end":17607972,"strand":1,"description":"leucine aminopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:18449]"}, {"versioned_ensembl_gene_id":"ENSG00000249502.1","gene_symbol":"AC006160.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17587467,"end":17614571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275066.4","gene_symbol":"SYNRG","gene_name":"synergin gamma [Source:HGNC Symbol;Acc:HGNC:557]","synonyms":"SYNG,MGC104959,AP1GBP1","biotype":"protein_coding","ncbi_id":"11276","summary":"This gene encodes a protein that interacts with the gamma subunit of AP1 clathrin-adaptor complex. The AP1 complex is located at the trans-Golgi network and associates specific proteins with clathrin-coated vesicles. This encoded protein may act to connect the AP1 complex to other proteins. Alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":37514797,"end":37609496,"strand":-1,"description":"synergin gamma [Source:HGNC Symbol;Acc:HGNC:557]"}, {"versioned_ensembl_gene_id":"ENSG00000240056.2","gene_symbol":"AL445190.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134941392,"end":134942450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118514.13","gene_symbol":"ALDH8A1","gene_name":"aldehyde dehydrogenase 8 family member A1 [Source:HGNC Symbol;Acc:HGNC:15471]","synonyms":"ALDH12","biotype":"protein_coding","ncbi_id":"64577","summary":"This gene encodes a member of the aldehyde dehydrogenase family of proteins. The encoded protein has been implicated in the synthesis of 9-cis-retinoic acid and in the breakdown of the amino acid tryptophan. This enzyme converts 9-cis-retinal into the retinoid X receptor ligand 9-cis-retinoic acid, and has approximately 40-fold higher activity with 9-cis-retinal than with all-trans-retinal. In addition, this enzyme has been shown to catalyze the conversion of 2-aminomuconic semialdehyde to 2-aminomuconate in the kynurenine pathway of tryptophan catabolism. [provided by RefSeq, Jul 2018]","start":134917390,"end":134950122,"strand":-1,"description":"aldehyde dehydrogenase 8 family member A1 [Source:HGNC Symbol;Acc:HGNC:15471]"}, {"versioned_ensembl_gene_id":"ENSG00000250017.1","gene_symbol":"AC117529.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45574590,"end":45576612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227543.4","gene_symbol":"SPAG5-AS1","gene_name":"SPAG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41140]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506436","summary":null,"start":28598790,"end":28617377,"strand":1,"description":"SPAG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41140]"}, {"versioned_ensembl_gene_id":"ENSG00000249433.1","gene_symbol":"AC008628.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115493557,"end":115493821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249026.2","gene_symbol":"CTNNA1P1","gene_name":"catenin alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2513]","synonyms":"CTNNAP1","biotype":"processed_pseudogene","ncbi_id":"1498","summary":null,"start":115389643,"end":115392370,"strand":-1,"description":"catenin alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2513]"}, {"versioned_ensembl_gene_id":"ENSG00000135378.3","gene_symbol":"PRRG4","gene_name":"proline rich and Gla domain 4 [Source:HGNC Symbol;Acc:HGNC:30799]","synonyms":"TMG4","biotype":"protein_coding","ncbi_id":"79056","summary":null,"start":32829943,"end":32858123,"strand":1,"description":"proline rich and Gla domain 4 [Source:HGNC Symbol;Acc:HGNC:30799]"}, {"versioned_ensembl_gene_id":"ENSG00000229991.1","gene_symbol":"AKR1B1P1","gene_name":"aldehyde reductase family 1 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:420]","synonyms":"ALDRL1","biotype":"processed_pseudogene","ncbi_id":"401982","summary":null,"start":224574434,"end":224575389,"strand":1,"description":"aldehyde reductase family 1 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:420]"}, {"versioned_ensembl_gene_id":"ENSG00000173418.11","gene_symbol":"NAA20","gene_name":"N(alpha)-acetyltransferase 20, NatB catalytic subunit [Source:HGNC Symbol;Acc:HGNC:15908]","synonyms":"NAT5,NAT3,dJ1002M8.1","biotype":"protein_coding","ncbi_id":"51126","summary":"NAT5 is a component of N-acetyltransferase complex B (NatB). Human NatB performs cotranslational N(alpha)-terminal acetylation of methionine residues when they are followed by asparagine (Starheim et al., 2008 [PubMed 18570629]).[supplied by OMIM, Apr 2009]","start":20017116,"end":20033655,"strand":1,"description":"N(alpha)-acetyltransferase 20, NatB catalytic subunit [Source:HGNC Symbol;Acc:HGNC:15908]"}, {"versioned_ensembl_gene_id":"ENSG00000280173.1","gene_symbol":"AC104447.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47346950,"end":47349073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099282.9","gene_symbol":"TSPAN15","gene_name":"tetraspanin 15 [Source:HGNC Symbol;Acc:HGNC:23298]","synonyms":"TM4SF15,NET-7","biotype":"protein_coding","ncbi_id":"23555","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":69451473,"end":69507669,"strand":1,"description":"tetraspanin 15 [Source:HGNC Symbol;Acc:HGNC:23298]"}, {"versioned_ensembl_gene_id":"ENSG00000230845.1","gene_symbol":"GSTA10P","gene_name":"glutathione S-transferase alpha 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:49904]","synonyms":"GSTAP2","biotype":"unprocessed_pseudogene","ncbi_id":"647177","summary":null,"start":52873014,"end":52879940,"strand":-1,"description":"glutathione S-transferase alpha 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:49904]"}, {"versioned_ensembl_gene_id":"ENSG00000263970.1","gene_symbol":"AP001094.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8406761,"end":8406953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281988.1","gene_symbol":"GRK1","gene_name":"G protein-coupled receptor kinase 1 [Source:HGNC Symbol;Acc:HGNC:10013]","synonyms":"RK,RHOK,GPRK1","biotype":"protein_coding","ncbi_id":"6011","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates rhodopsin and initiates its deactivation. Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2). [provided by RefSeq, Jul 2008]","start":113731864,"end":113738248,"strand":1,"description":"G protein-coupled receptor kinase 1 [Source:HGNC Symbol;Acc:HGNC:10013]"}, {"versioned_ensembl_gene_id":"ENSG00000276795.1","gene_symbol":"AL391987.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61912704,"end":61913115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218052.5","gene_symbol":"ADAMTS7P4","gene_name":"ADAMTS7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49410]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"642935","summary":null,"start":85255369,"end":85330334,"strand":-1,"description":"ADAMTS7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49410]"}, {"versioned_ensembl_gene_id":"ENSG00000280938.1","gene_symbol":"TUSC5","gene_name":"tumor suppressor candidate 5 [Source:HGNC Symbol;Acc:HGNC:29592]","synonyms":"LOST1,IFITMD3,BEC-1","biotype":"polymorphic_pseudogene","ncbi_id":"286753","summary":null,"start":1201029,"end":1203765,"strand":1,"description":"tumor suppressor candidate 5 [Source:HGNC Symbol;Acc:HGNC:29592]"}, {"versioned_ensembl_gene_id":"ENSG00000235849.1","gene_symbol":"HS6ST2-AS1","gene_name":"HS6ST2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40870]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874102","summary":null,"start":132667642,"end":132669888,"strand":1,"description":"HS6ST2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40870]"}, {"versioned_ensembl_gene_id":"ENSG00000255299.5","gene_symbol":"AP003557.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58497888,"end":58505758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219626.8","gene_symbol":"FAM228B","gene_name":"family with sequence similarity 228 member B [Source:HGNC Symbol;Acc:HGNC:24736]","synonyms":null,"biotype":"protein_coding","ncbi_id":"375190","summary":null,"start":24076526,"end":24169640,"strand":1,"description":"family with sequence similarity 228 member B [Source:HGNC Symbol;Acc:HGNC:24736]"}, {"versioned_ensembl_gene_id":"ENSG00000172365.3","gene_symbol":"OR5B2","gene_name":"olfactory receptor family 5 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:8323]","synonyms":"OST073","biotype":"protein_coding","ncbi_id":"390190","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58421264,"end":58428121,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:8323]"}, {"versioned_ensembl_gene_id":"ENSG00000227592.1","gene_symbol":"PIGFP3","gene_name":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129049","summary":null,"start":30017160,"end":30017881,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45151]"}, {"versioned_ensembl_gene_id":"ENSG00000236471.1","gene_symbol":"AF127577.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15067070,"end":15067837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225043.1","gene_symbol":"RPL18AP2","gene_name":"ribosomal protein L18a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387494","summary":null,"start":46420553,"end":46421034,"strand":-1,"description":"ribosomal protein L18a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23774]"}, {"versioned_ensembl_gene_id":"ENSG00000090776.5","gene_symbol":"EFNB1","gene_name":"ephrin B1 [Source:HGNC Symbol;Acc:HGNC:3226]","synonyms":"EPLG2,Elk-L,CFNS,LERK2","biotype":"protein_coding","ncbi_id":"1947","summary":"The protein encoded by this gene is a type I membrane protein and a ligand of Eph-related receptor tyrosine kinases. It may play a role in cell adhesion and function in the development or maintenance of the nervous system. [provided by RefSeq, Jul 2008]","start":68828997,"end":68842147,"strand":1,"description":"ephrin B1 [Source:HGNC Symbol;Acc:HGNC:3226]"}, {"versioned_ensembl_gene_id":"ENSG00000276118.1","gene_symbol":"AC242852.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143343180,"end":143343275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278434.1","gene_symbol":"AC023830.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4532216,"end":4533670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276708.2","gene_symbol":"IGHV5-78","gene_name":"immunoglobulin heavy variable 5-78 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5660]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28387","summary":null,"start":106875299,"end":106875593,"strand":-1,"description":"immunoglobulin heavy variable 5-78 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5660]"}, {"versioned_ensembl_gene_id":"ENSG00000046653.14","gene_symbol":"GPM6B","gene_name":"glycoprotein M6B [Source:HGNC Symbol;Acc:HGNC:4461]","synonyms":"MGC54284,MGC17150,M6B","biotype":"protein_coding","ncbi_id":"2824","summary":"This gene encodes a membrane glycoprotein that belongs to the proteolipid protein family. Proteolipid protein family members are expressed in most brain regions and are thought to be involved in cellular housekeeping functions such as membrane trafficking and cell-to-cell communication. This protein may also be involved in osteoblast differentiation. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are located on chromosomes Y and 22. [provided by RefSeq, Jan 2016]","start":13771031,"end":13938638,"strand":-1,"description":"glycoprotein M6B [Source:HGNC Symbol;Acc:HGNC:4461]"}, {"versioned_ensembl_gene_id":"ENSG00000033800.13","gene_symbol":"PIAS1","gene_name":"protein inhibitor of activated STAT 1 [Source:HGNC Symbol;Acc:HGNC:2752]","synonyms":"ZMIZ3,GU/RH-II,GBP,DDXBP1","biotype":"protein_coding","ncbi_id":"8554","summary":"This gene encodes a member of the protein inhibitor of activated STAT (PIAS) family. PIAS proteins function as SUMO E3 ligases and play important roles in many cellular processes by mediating the sumoylation of target proteins. This protein plays a central role as a transcriptional coregulator of numerous cellular pathways includign the STAT1 and nuclear factor kappaB pathways. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":68054179,"end":68198603,"strand":1,"description":"protein inhibitor of activated STAT 1 [Source:HGNC Symbol;Acc:HGNC:2752]"}, {"versioned_ensembl_gene_id":"ENSG00000269984.1","gene_symbol":"AC078795.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169777192,"end":169780334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224941.6","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31203494,"end":31209123,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000224579.1","gene_symbol":"AC245052.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54209092,"end":54209418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263716.1","gene_symbol":"SLC25A51P2","gene_name":"solute carrier family 25 member 51 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23327]","synonyms":"MCART4P","biotype":"processed_pseudogene","ncbi_id":"645423","summary":null,"start":7134931,"end":7135819,"strand":1,"description":"solute carrier family 25 member 51 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23327]"}, {"versioned_ensembl_gene_id":"ENSG00000257009.1","gene_symbol":"AC022367.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25585994,"end":25592928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279173.1","gene_symbol":"AC092451.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25423600,"end":25424942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257865.1","gene_symbol":"AC090022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60418983,"end":60419293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203527.2","gene_symbol":"Z99756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43275955,"end":43283830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130340.15","gene_symbol":"SNX9","gene_name":"sorting nexin 9 [Source:HGNC Symbol;Acc:HGNC:14973]","synonyms":"SH3PXD3A,SH3PX1,SDP1","biotype":"protein_coding","ncbi_id":"51429","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phosphoinositide binding domain, and are involved in intracellular trafficking. The encoded protein does not contain a coiled coil region, like some family members, but does contain a SRC homology domain near its N-terminus. The encoded protein is reported to have a variety of interaction partners, including of adaptor protein 2 , dynamin, tyrosine kinase non-receptor 2, Wiskott-Aldrich syndrome-like, and ARP3 actin-related protein 3. The encoded protein is implicated in several stages of intracellular trafficking, including endocytosis, macropinocytosis, and F-actin nucleation. [provided by RefSeq, Jul 2013]","start":157700387,"end":157945077,"strand":1,"description":"sorting nexin 9 [Source:HGNC Symbol;Acc:HGNC:14973]"}, {"versioned_ensembl_gene_id":"ENSG00000262334.6","gene_symbol":"RPH3AL","gene_name":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]","synonyms":"Noc2","biotype":"protein_coding","ncbi_id":"9501","summary":"The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]","start":217541,"end":419308,"strand":-1,"description":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]"}, {"versioned_ensembl_gene_id":"ENSG00000270185.1","gene_symbol":"IGHD1OR15-1B","gene_name":"immunoglobulin heavy diversity 1/OR15-1B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5488]","synonyms":"IGHD1OR151B,IGHD1/OR15-1B","biotype":"IG_D_gene","ncbi_id":"28334","summary":null,"start":21017800,"end":21017816,"strand":-1,"description":"immunoglobulin heavy diversity 1/OR15-1B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5488]"}, {"versioned_ensembl_gene_id":"ENSG00000112183.14","gene_symbol":"RBM24","gene_name":"RNA binding motif protein 24 [Source:HGNC Symbol;Acc:HGNC:21539]","synonyms":"RNPC6,FLJ30829,dJ259A10.1","biotype":"protein_coding","ncbi_id":"221662","summary":null,"start":17281346,"end":17293875,"strand":1,"description":"RNA binding motif protein 24 [Source:HGNC Symbol;Acc:HGNC:21539]"}, {"versioned_ensembl_gene_id":"ENSG00000215915.9","gene_symbol":"ATAD3C","gene_name":"ATPase family, AAA domain containing 3C [Source:HGNC Symbol;Acc:HGNC:32151]","synonyms":"FLJ34599","biotype":"protein_coding","ncbi_id":"219293","summary":null,"start":1449689,"end":1470158,"strand":1,"description":"ATPase family, AAA domain containing 3C [Source:HGNC Symbol;Acc:HGNC:32151]"}, {"versioned_ensembl_gene_id":"ENSG00000213740.2","gene_symbol":"SERBP1P1","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32247]","synonyms":"SERBP1P","biotype":"processed_pseudogene","ncbi_id":"389866","summary":null,"start":68783472,"end":68785066,"strand":1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32247]"}, {"versioned_ensembl_gene_id":"ENSG00000237269.1","gene_symbol":"RBMY2TP","gene_name":"RNA binding motif protein, Y-linked, family 2, member T pseudogene [Source:HGNC Symbol;Acc:HGNC:23897]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379008","summary":null,"start":21430697,"end":21437245,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member T pseudogene [Source:HGNC Symbol;Acc:HGNC:23897]"}, {"versioned_ensembl_gene_id":"ENSG00000165553.4","gene_symbol":"NGB","gene_name":"neuroglobin [Source:HGNC Symbol;Acc:HGNC:14077]","synonyms":null,"biotype":"protein_coding","ncbi_id":"58157","summary":"This gene encodes an oxygen-binding protein that is distantly related to members of the globin gene family. It is highly conserved among other vertebrates. It is expressed in the central and peripheral nervous system where it may be involved in increasing oxygen availability and providing protection under hypoxic/ischemic conditions. [provided by RefSeq, Jul 2008]","start":77265483,"end":77271312,"strand":-1,"description":"neuroglobin [Source:HGNC Symbol;Acc:HGNC:14077]"}, {"versioned_ensembl_gene_id":"ENSG00000223960.6","gene_symbol":"AC009948.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178413939,"end":178440243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280288.1","gene_symbol":"AC131935.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":11725332,"end":11726702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247033.1","gene_symbol":"AC099508.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75108601,"end":75110712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256904.1","gene_symbol":"A2ML1-AS2","gene_name":"A2ML1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41523]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478979","summary":null,"start":8819816,"end":8820713,"strand":-1,"description":"A2ML1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41523]"}, {"versioned_ensembl_gene_id":"ENSG00000268266.1","gene_symbol":"AC003005.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57477649,"end":57482996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275417.1","gene_symbol":"AC068726.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56248787,"end":56249127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244921.2","gene_symbol":"MTCYBP18","gene_name":"mitochondrially encoded cytochrome b pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075130","summary":null,"start":134923303,"end":134924049,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51976]"}, {"versioned_ensembl_gene_id":"ENSG00000273876.1","gene_symbol":"AC019176.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5127919,"end":5128233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257671.1","gene_symbol":"KRT7-AS","gene_name":"KRT7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52643]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"109729127","summary":null,"start":52245048,"end":52247448,"strand":-1,"description":"KRT7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52643]"}, {"versioned_ensembl_gene_id":"ENSG00000227970.1","gene_symbol":"NR1H5P","gene_name":"nuclear receptor subfamily 1 group H member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32673]","synonyms":"NR1H5,Fxrb","biotype":"unitary_pseudogene","ncbi_id":"643609","summary":null,"start":114837227,"end":114851453,"strand":1,"description":"nuclear receptor subfamily 1 group H member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32673]"}, {"versioned_ensembl_gene_id":"ENSG00000183569.17","gene_symbol":"SERHL2","gene_name":"serine hydrolase like 2 [Source:HGNC Symbol;Acc:HGNC:29446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253190","summary":null,"start":42553617,"end":42574382,"strand":1,"description":"serine hydrolase like 2 [Source:HGNC Symbol;Acc:HGNC:29446]"}, {"versioned_ensembl_gene_id":"ENSG00000181915.4","gene_symbol":"ADO","gene_name":"2-aminoethanethiol dioxygenase [Source:HGNC Symbol;Acc:HGNC:23506]","synonyms":"FLJ14547,C10orf22","biotype":"protein_coding","ncbi_id":"84890","summary":"Human thiol dioxygenases include cysteine dioxygenase (CDO; MIM 603943) and cysteamine (2-aminoethanethiol) dioxygenase (ADO; EC 1.13.11.19). CDO adds 2 oxygen atoms to free cysteine, whereas ADO adds 2 oxygen atoms to free cysteamine to form hypotaurine (Dominy et al., 2007 [PubMed 17581819]).[supplied by OMIM, Mar 2008]","start":62804857,"end":62808483,"strand":1,"description":"2-aminoethanethiol dioxygenase [Source:HGNC Symbol;Acc:HGNC:23506]"}, {"versioned_ensembl_gene_id":"ENSG00000182379.9","gene_symbol":"NXPH4","gene_name":"neurexophilin 4 [Source:HGNC Symbol;Acc:HGNC:8078]","synonyms":"NPH4","biotype":"protein_coding","ncbi_id":"11247","summary":null,"start":57216795,"end":57226449,"strand":1,"description":"neurexophilin 4 [Source:HGNC Symbol;Acc:HGNC:8078]"}, {"versioned_ensembl_gene_id":"ENSG00000272857.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859616,"end":28863341,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000186513.3","gene_symbol":"OR9Q2","gene_name":"olfactory receptor family 9 subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:15328]","synonyms":"OR9Q2P","biotype":"protein_coding","ncbi_id":"219957","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58189070,"end":58194053,"strand":1,"description":"olfactory receptor family 9 subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:15328]"}, {"versioned_ensembl_gene_id":"ENSG00000283967.1","gene_symbol":"AC233724.18","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17590364,"end":17590960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272793.1","gene_symbol":"CR759954.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837861,"end":28838998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271108.1","gene_symbol":"KATNBL1P5","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420841","summary":null,"start":25248263,"end":25248779,"strand":1,"description":"katanin regulatory subunit B1 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49055]"}, {"versioned_ensembl_gene_id":"ENSG00000153443.12","gene_symbol":"UBALD1","gene_name":"UBA like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29576]","synonyms":"FAM100A","biotype":"protein_coding","ncbi_id":"124402","summary":null,"start":4608883,"end":4615027,"strand":-1,"description":"UBA like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29576]"}, {"versioned_ensembl_gene_id":"ENSG00000255266.1","gene_symbol":"AP003484.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57870322,"end":57870571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225285.1","gene_symbol":"LINC01770","gene_name":"long intergenic non-protein coding RNA 1770 [Source:HGNC Symbol;Acc:HGNC:52560]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724312","summary":null,"start":1430539,"end":1434573,"strand":-1,"description":"long intergenic non-protein coding RNA 1770 [Source:HGNC Symbol;Acc:HGNC:52560]"}, {"versioned_ensembl_gene_id":"ENSG00000275628.2","gene_symbol":"AL590491.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":60918581,"end":60927822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100387.8","gene_symbol":"RBX1","gene_name":"ring-box 1 [Source:HGNC Symbol;Acc:HGNC:9928]","synonyms":"ROC1,RNF75,BA554C12.1","biotype":"protein_coding","ncbi_id":"9978","summary":"This locus encodes a RING finger-like domain-containing protein. The encoded protein interacts with cullin proteins and likely plays a role in ubiquitination processes necessary for cell cycle progression. This protein may also affect protein turnover. Related pseudogenes exist on chromosomes 2 and 5.[provided by RefSeq, Sep 2010]","start":40951347,"end":40973309,"strand":1,"description":"ring-box 1 [Source:HGNC Symbol;Acc:HGNC:9928]"}, {"versioned_ensembl_gene_id":"ENSG00000213862.4","gene_symbol":"AC044787.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47730144,"end":47730935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276156.1","gene_symbol":"AL138880.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45097496,"end":45097976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168066.20","gene_symbol":"SF1","gene_name":"splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:12950]","synonyms":"ZNF162,ZFM1,ZCCHC25","biotype":"protein_coding","ncbi_id":"7536","summary":"This gene encodes a nuclear pre-mRNA splicing factor. The encoded protein specifically recognizes the intron branch point sequence at the 3' splice site, together with the large subunit of U2 auxiliary factor (U2AF), and is required for the early stages of spliceosome assembly. It also plays a role in nuclear pre-mRNA retention and transcriptional repression. The encoded protein contains an N-terminal U2AF ligand motif, a central hnRNP K homology motif and quaking 2 region which bind a key branch-site adenosine within the branch point sequence, a zinc knuckles domain, and a C-terminal proline-rich domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":64764606,"end":64778786,"strand":-1,"description":"splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:12950]"}, {"versioned_ensembl_gene_id":"ENSG00000266290.1","gene_symbol":"AC015813.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58076891,"end":58083204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230523.1","gene_symbol":"LINC01756","gene_name":"long intergenic non-protein coding RNA 1756 [Source:HGNC Symbol;Acc:HGNC:52545]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928460","summary":null,"start":29329620,"end":29350114,"strand":-1,"description":"long intergenic non-protein coding RNA 1756 [Source:HGNC Symbol;Acc:HGNC:52545]"}, {"versioned_ensembl_gene_id":"ENSG00000119820.10","gene_symbol":"YIPF4","gene_name":"Yip1 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:28145]","synonyms":"MGC11061,FinGER4","biotype":"protein_coding","ncbi_id":"84272","summary":null,"start":32277910,"end":32316594,"strand":1,"description":"Yip1 domain family member 4 [Source:HGNC Symbol;Acc:HGNC:28145]"}, {"versioned_ensembl_gene_id":"ENSG00000282518.1","gene_symbol":"AC240565.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97494,"end":118578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270432.1","gene_symbol":"OR7E108P","gene_name":"olfactory receptor family 7 subfamily E member 108 pseudogene [Source:HGNC Symbol;Acc:HGNC:15117]","synonyms":"OST726","biotype":"unprocessed_pseudogene","ncbi_id":"81363","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":90751240,"end":90752230,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 108 pseudogene [Source:HGNC Symbol;Acc:HGNC:15117]"}, {"versioned_ensembl_gene_id":"ENSG00000226953.7","gene_symbol":"AC010890.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133264968,"end":133284762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213928.8","gene_symbol":"IRF9","gene_name":"interferon regulatory factor 9 [Source:HGNC Symbol;Acc:HGNC:6131]","synonyms":"ISGF3G","biotype":"protein_coding","ncbi_id":"10379","summary":"This gene encodes a member of the interferon regulatory factor (IRF) family, a group of transcription factors with diverse roles, including virus-mediated activation of interferon, and modulation of cell growth, differentiation, apoptosis, and immune system activity. Members of the IRF family are characterized by a conserved N-terminal DNA-binding domain containing tryptophan (W) repeats. Mutations in this gene result in Immunodeficiency 65. [provided by RefSeq, Jul 2020]","start":24161053,"end":24166565,"strand":1,"description":"interferon regulatory factor 9 [Source:HGNC Symbol;Acc:HGNC:6131]"}, {"versioned_ensembl_gene_id":"ENSG00000220514.1","gene_symbol":"MTND4LP20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42254]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075242","summary":null,"start":153668589,"end":153668858,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42254]"}, {"versioned_ensembl_gene_id":"ENSG00000181264.8","gene_symbol":"TMEM136","gene_name":"transmembrane protein 136 [Source:HGNC Symbol;Acc:HGNC:28280]","synonyms":"MGC17839","biotype":"protein_coding","ncbi_id":"219902","summary":null,"start":120325129,"end":120333682,"strand":1,"description":"transmembrane protein 136 [Source:HGNC Symbol;Acc:HGNC:28280]"}, {"versioned_ensembl_gene_id":"ENSG00000270576.1","gene_symbol":"AC005520.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73840520,"end":73840609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196459.13","gene_symbol":"TRAPPC2","gene_name":"trafficking protein particle complex 2 [Source:HGNC Symbol;Acc:HGNC:23068]","synonyms":"ZNF547L,TRS20,SEDT,SEDL,MIP-2A,hYP38334","biotype":"protein_coding","ncbi_id":"6399","summary":"The protein encoded by this gene is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]","start":13712244,"end":13734635,"strand":-1,"description":"trafficking protein particle complex 2 [Source:HGNC Symbol;Acc:HGNC:23068]"}, {"versioned_ensembl_gene_id":"ENSG00000119782.13","gene_symbol":"FKBP1B","gene_name":"FK506 binding protein 1B [Source:HGNC Symbol;Acc:HGNC:3712]","synonyms":"PPIase,OTK4,FKBP9,FKBP1L,FKBP12.6","biotype":"protein_coding","ncbi_id":"2281","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It is highly similar to the FK506-binding protein 1A. Its physiological role is thought to be in excitation-contraction coupling in cardiac muscle. There are two alternatively spliced transcript variants of this gene encoding different isoforms. [provided by RefSeq, Jul 2008]","start":24049701,"end":24063681,"strand":1,"description":"FK506 binding protein 1B [Source:HGNC Symbol;Acc:HGNC:3712]"}, {"versioned_ensembl_gene_id":"ENSG00000258676.4","gene_symbol":"AC091544.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":92580829,"end":92600545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274752.1","gene_symbol":"AC244196.1","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142560423,"end":142560931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213338.3","gene_symbol":"ATF4P1","gene_name":"activating transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:789]","synonyms":"TXREBP,TAXREB67P,ATF4P","biotype":"processed_pseudogene","ncbi_id":"469","summary":null,"start":154622428,"end":154623500,"strand":-1,"description":"activating transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:789]"}, {"versioned_ensembl_gene_id":"ENSG00000261218.5","gene_symbol":"AC099524.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81738248,"end":81767868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258656.1","gene_symbol":"AL160236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60972272,"end":60972466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188785.11","gene_symbol":"ZNF548","gene_name":"zinc finger protein 548 [Source:HGNC Symbol;Acc:HGNC:26561]","synonyms":"FLJ32932","biotype":"protein_coding","ncbi_id":"147694","summary":null,"start":57389850,"end":57402992,"strand":1,"description":"zinc finger protein 548 [Source:HGNC Symbol;Acc:HGNC:26561]"}, {"versioned_ensembl_gene_id":"ENSG00000215196.4","gene_symbol":"AC026790.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17130028,"end":17217047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268967.1","gene_symbol":"AC119751.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49548564,"end":49548855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273989.1","gene_symbol":"AC022079.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28236227,"end":28236828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110697.12","gene_symbol":"PITPNM1","gene_name":"phosphatidylinositol transfer protein membrane associated 1 [Source:HGNC Symbol;Acc:HGNC:9003]","synonyms":"NIR2,DRES9,RDGBA1,RDGB1,RDGB,Rd9,PITPNM","biotype":"protein_coding","ncbi_id":"9600","summary":"PITPNM1 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]","start":67491768,"end":67506263,"strand":-1,"description":"phosphatidylinositol transfer protein membrane associated 1 [Source:HGNC Symbol;Acc:HGNC:9003]"}, {"versioned_ensembl_gene_id":"ENSG00000242385.1","gene_symbol":"LINC00901","gene_name":"long intergenic non-protein coding RNA 901 [Source:HGNC Symbol;Acc:HGNC:40352]","synonyms":"TCONS_00005428,LSAMP-AS4,BC040587","biotype":"antisense_RNA","ncbi_id":"100506724","summary":null,"start":116921431,"end":116932238,"strand":1,"description":"long intergenic non-protein coding RNA 901 [Source:HGNC Symbol;Acc:HGNC:40352]"}, {"versioned_ensembl_gene_id":"ENSG00000160883.10","gene_symbol":"HK3","gene_name":"hexokinase 3 [Source:HGNC Symbol;Acc:HGNC:4925]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3101","summary":"Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes hexokinase 3. Similar to hexokinases 1 and 2, this allosteric enzyme is inhibited by its product glucose-6-phosphate. [provided by RefSeq, Apr 2009]","start":176880869,"end":176899332,"strand":-1,"description":"hexokinase 3 [Source:HGNC Symbol;Acc:HGNC:4925]"}, {"versioned_ensembl_gene_id":"ENSG00000267561.2","gene_symbol":"AC093155.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":86993009,"end":87169204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074047.21","gene_symbol":"GLI2","gene_name":"GLI family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:4318]","synonyms":"THP2,THP1,HPE9","biotype":"protein_coding","ncbi_id":"2736","summary":"This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008]","start":120735623,"end":120992653,"strand":1,"description":"GLI family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:4318]"}, {"versioned_ensembl_gene_id":"ENSG00000271709.1","gene_symbol":"AC017033.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120866378,"end":120867403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278626.1","gene_symbol":"AC023310.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20642799,"end":20643448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251446.1","gene_symbol":"AC113391.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176726942,"end":176739458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196101.9","gene_symbol":"HLA-DRB3","gene_name":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]","synonyms":"HLA-DR3B,HLA-DR3B","biotype":"protein_coding","ncbi_id":"3125","summary":"HLA-DRB3 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32449765,"end":32462852,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]"}, {"versioned_ensembl_gene_id":"ENSG00000232903.2","gene_symbol":"LINC01166","gene_name":"long intergenic non-protein coding RNA 1166 [Source:HGNC Symbol;Acc:HGNC:49535]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927590","summary":null,"start":132943967,"end":132965289,"strand":-1,"description":"long intergenic non-protein coding RNA 1166 [Source:HGNC Symbol;Acc:HGNC:49535]"}, {"versioned_ensembl_gene_id":"ENSG00000163833.7","gene_symbol":"FBXO40","gene_name":"F-box protein 40 [Source:HGNC Symbol;Acc:HGNC:29816]","synonyms":"KIAA1195,Fbx40","biotype":"protein_coding","ncbi_id":"51725","summary":"Members of the F-box protein family, such as FBXO40, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":121593119,"end":121630295,"strand":1,"description":"F-box protein 40 [Source:HGNC Symbol;Acc:HGNC:29816]"}, {"versioned_ensembl_gene_id":"ENSG00000258445.3","gene_symbol":"AL132777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60779978,"end":60780595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169955.7","gene_symbol":"ZNF747","gene_name":"zinc finger protein 747 [Source:HGNC Symbol;Acc:HGNC:28350]","synonyms":"MGC2474","biotype":"protein_coding","ncbi_id":"65988","summary":null,"start":30530367,"end":30535347,"strand":-1,"description":"zinc finger protein 747 [Source:HGNC Symbol;Acc:HGNC:28350]"}, {"versioned_ensembl_gene_id":"ENSG00000154930.14","gene_symbol":"ACSS1","gene_name":"acyl-CoA synthetase short chain family member 1 [Source:HGNC Symbol;Acc:HGNC:16091]","synonyms":"MGC33843,dJ568C11.3,AceCS2L,ACAS2L","biotype":"protein_coding","ncbi_id":"84532","summary":"This gene encodes a mitochondrial acetyl-CoA synthetase enzyme. A similar protein in mice plays an important role in the tricarboxylic acid cycle by catalyzing the conversion of acetate to acetyl CoA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":25006230,"end":25058980,"strand":-1,"description":"acyl-CoA synthetase short chain family member 1 [Source:HGNC Symbol;Acc:HGNC:16091]"}, {"versioned_ensembl_gene_id":"ENSG00000232093.1","gene_symbol":"DCST1-AS1","gene_name":"DCST1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41147]","synonyms":"RP11-307C12.11","biotype":"antisense_RNA","ncbi_id":"100505666","summary":null,"start":155045191,"end":155046118,"strand":-1,"description":"DCST1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41147]"}, {"versioned_ensembl_gene_id":"ENSG00000248485.1","gene_symbol":"PCP4L1","gene_name":"Purkinje cell protein 4 like 1 [Source:HGNC Symbol;Acc:HGNC:20448]","synonyms":"IQM1","biotype":"protein_coding","ncbi_id":"654790","summary":null,"start":161258727,"end":161285450,"strand":1,"description":"Purkinje cell protein 4 like 1 [Source:HGNC Symbol;Acc:HGNC:20448]"}, {"versioned_ensembl_gene_id":"ENSG00000250041.2","gene_symbol":"AC069360.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10884885,"end":10899322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272158.1","gene_symbol":"AL139022.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65003325,"end":65003767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234898.1","gene_symbol":"CHEK2P3","gene_name":"checkpoint kinase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43579]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873791","summary":null,"start":91957436,"end":91963610,"strand":1,"description":"checkpoint kinase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43579]"}, {"versioned_ensembl_gene_id":"ENSG00000226036.1","gene_symbol":"AL590648.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":212647296,"end":212647755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232522.1","gene_symbol":"ZNF886P","gene_name":"zinc finger protein 886, pseudogene [Source:HGNC Symbol;Acc:HGNC:38420]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419728","summary":null,"start":20001185,"end":20012204,"strand":-1,"description":"zinc finger protein 886, pseudogene [Source:HGNC Symbol;Acc:HGNC:38420]"}, {"versioned_ensembl_gene_id":"ENSG00000253556.1","gene_symbol":"MTCO1P4","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480684","summary":null,"start":103088796,"end":103090671,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50350]"}, {"versioned_ensembl_gene_id":"ENSG00000196449.3","gene_symbol":"YRDC","gene_name":"yrdC N6-threonylcarbamoyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:28905]","synonyms":"SUA5,IRIP,FLJ23476","biotype":"protein_coding","ncbi_id":"79693","summary":null,"start":37802944,"end":37808185,"strand":-1,"description":"yrdC N6-threonylcarbamoyltransferase domain containing [Source:HGNC Symbol;Acc:HGNC:28905]"}, {"versioned_ensembl_gene_id":"ENSG00000275313.5","gene_symbol":"CCL4L2","gene_name":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9560","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this family member is similar to the chemokine (C-C motif) ligand 4 product, which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals, where most individuals have one to five copies. This gene copy contains a non-consensus splice acceptor site at the 3' terminal exon found in other highly similar gene copies, and it thus uses other alternative splice sites for the 3' terminal exon, resulting in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36312669,"end":36314484,"strand":1,"description":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]"}, {"versioned_ensembl_gene_id":"ENSG00000164123.6","gene_symbol":"C4orf45","gene_name":"chromosome 4 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:26342]","synonyms":"FLJ25371","biotype":"protein_coding","ncbi_id":"152940","summary":null,"start":158893134,"end":159038760,"strand":-1,"description":"chromosome 4 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:26342]"}, {"versioned_ensembl_gene_id":"ENSG00000172183.14","gene_symbol":"ISG20","gene_name":"interferon stimulated exonuclease gene 20 [Source:HGNC Symbol;Acc:HGNC:6130]","synonyms":"HEM45,CD25","biotype":"protein_coding","ncbi_id":"3669","summary":null,"start":88636153,"end":88656483,"strand":1,"description":"interferon stimulated exonuclease gene 20 [Source:HGNC Symbol;Acc:HGNC:6130]"}, {"versioned_ensembl_gene_id":"ENSG00000248396.1","gene_symbol":"TOMM22P4","gene_name":"TOMM22 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874517","summary":null,"start":162521682,"end":162522041,"strand":1,"description":"TOMM22 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38740]"}, {"versioned_ensembl_gene_id":"ENSG00000248988.1","gene_symbol":"AC093700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159007119,"end":159007835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239323.1","gene_symbol":"AL163973.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31462795,"end":31463371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228429.1","gene_symbol":"AC004910.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68640798,"end":68641584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266120.1","gene_symbol":"AC104984.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30238741,"end":30252237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165688.11","gene_symbol":"PMPCA","gene_name":"peptidase, mitochondrial processing alpha subunit [Source:HGNC Symbol;Acc:HGNC:18667]","synonyms":"KIAA0123,INPP5E,Alpha-MPP","biotype":"protein_coding","ncbi_id":"23203","summary":"The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2. [provided by RefSeq, Mar 2016]","start":136410570,"end":136423761,"strand":1,"description":"peptidase, mitochondrial processing alpha subunit [Source:HGNC Symbol;Acc:HGNC:18667]"}, {"versioned_ensembl_gene_id":"ENSG00000157916.19","gene_symbol":"RER1","gene_name":"retention in endoplasmic reticulum sorting receptor 1 [Source:HGNC Symbol;Acc:HGNC:30309]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11079","summary":"The protein encoded by this gene is a multi-pass membrane protein that is localized to the golgi apparatus. It is involved in the retention of endoplasmic reticulum (ER) membrane proteins in the ER and retrieval of ER membrane proteins from the early Golgi compartment to facilitate gamma-secretase complex assembly. [provided by RefSeq, Oct 2009]","start":2391775,"end":2405444,"strand":1,"description":"retention in endoplasmic reticulum sorting receptor 1 [Source:HGNC Symbol;Acc:HGNC:30309]"}, {"versioned_ensembl_gene_id":"ENSG00000241307.1","gene_symbol":"AC104472.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155760617,"end":155761217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227497.1","gene_symbol":"PABPC1P6","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37986]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128696","summary":null,"start":91877969,"end":91880195,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37986]"}, {"versioned_ensembl_gene_id":"ENSG00000083844.10","gene_symbol":"ZNF264","gene_name":"zinc finger protein 264 [Source:HGNC Symbol;Acc:HGNC:13057]","synonyms":"KIAA0412","biotype":"protein_coding","ncbi_id":"9422","summary":"This gene encodes a zinc finger protein and belongs to the krueppel C2H2-type zinc-finger protein family. Zinc finger proteins are often localized in the nucleus, bind nucleic acids, and regulate transcription. [provided by RefSeq, Jan 2010]","start":57191500,"end":57222846,"strand":1,"description":"zinc finger protein 264 [Source:HGNC Symbol;Acc:HGNC:13057]"}, {"versioned_ensembl_gene_id":"ENSG00000237085.2","gene_symbol":"AC127391.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91859384,"end":91859481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281848.1","gene_symbol":"AC093724.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131723253,"end":131724279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235235.6","gene_symbol":"IGKV1OR2-1","gene_name":"immunoglobulin kappa variable 1/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5760]","synonyms":"IGKVPZ1,IGKV1OR-1,IGKV1/OR2-1,IGKV1/OR-1","biotype":"IG_V_pseudogene","ncbi_id":"3531","summary":null,"start":91817771,"end":91818248,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5760]"}, {"versioned_ensembl_gene_id":"ENSG00000258873.2","gene_symbol":"DUXA","gene_name":"double homeobox A [Source:HGNC Symbol;Acc:HGNC:32179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503835","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the DUXA homeobox gene family. Evidence of mRNA expression has not yet been found for this gene. Multiple, related processed pseudogenes have been found which are thought to reflect expression of this gene in the germ line or embryonic cells. [provided by RefSeq, Jul 2008]","start":57154021,"end":57167443,"strand":-1,"description":"double homeobox A [Source:HGNC Symbol;Acc:HGNC:32179]"}, {"versioned_ensembl_gene_id":"ENSG00000232628.5","gene_symbol":"AC092809.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":224208747,"end":224213279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164109.13","gene_symbol":"MAD2L1","gene_name":"mitotic arrest deficient 2 like 1 [Source:HGNC Symbol;Acc:HGNC:6763]","synonyms":"MAD2,HSMAD2","biotype":"protein_coding","ncbi_id":"4085","summary":"MAD2L1 is a component of the mitotic spindle assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. MAD2L1 is related to the MAD2L2 gene located on chromosome 1. A MAD2 pseudogene has been mapped to chromosome 14. [provided by RefSeq, Jul 2008]","start":120055608,"end":120067074,"strand":-1,"description":"mitotic arrest deficient 2 like 1 [Source:HGNC Symbol;Acc:HGNC:6763]"}, {"versioned_ensembl_gene_id":"ENSG00000249713.1","gene_symbol":"AC026725.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76606608,"end":76608970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282305.1","gene_symbol":"IGHV3-74","gene_name":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28408","summary":null,"start":106834616,"end":106835307,"strand":-1,"description":"immunoglobulin heavy variable 3-74 [Source:HGNC Symbol;Acc:HGNC:5624]"}, {"versioned_ensembl_gene_id":"ENSG00000255354.1","gene_symbol":"AC022239.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11558466,"end":11560020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006704.10","gene_symbol":"GTF2IRD1","gene_name":"GTF2I repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:4661]","synonyms":"MusTRD1,GTF3,Cream1,BEN,WBSCR12,WBSCR11,RBAP2","biotype":"protein_coding","ncbi_id":"9569","summary":"The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":74453790,"end":74602604,"strand":1,"description":"GTF2I repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:4661]"}, {"versioned_ensembl_gene_id":"ENSG00000100012.11","gene_symbol":"SEC14L3","gene_name":"SEC14 like lipid binding 3 [Source:HGNC Symbol;Acc:HGNC:18655]","synonyms":"TAP2","biotype":"protein_coding","ncbi_id":"266629","summary":"The protein encoded by this gene is highly similar to the protein encoded by the Saccharomyces cerevisiae SEC14 gene. The SEC14 protein is a phophatidylinositol transfer protein that is essential for biogenesis of Golgi-derived transport vesicles, and thus is required for the export of yeast secretory proteins from the Golgi complex. The specific function of this protein has not yet been determined. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30447959,"end":30472049,"strand":-1,"description":"SEC14 like lipid binding 3 [Source:HGNC Symbol;Acc:HGNC:18655]"}, {"versioned_ensembl_gene_id":"ENSG00000271377.1","gene_symbol":"AC113143.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60906059,"end":60906452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008086.11","gene_symbol":"CDKL5","gene_name":"cyclin dependent kinase like 5 [Source:HGNC Symbol;Acc:HGNC:11411]","synonyms":"CFAP247,STK9,EIEE2","biotype":"protein_coding","ncbi_id":"6792","summary":"This gene is a member of Ser/Thr protein kinase family and encodes a phosphorylated protein with protein kinase activity. Mutations in this gene have been associated with X-linked infantile spasm syndrome (ISSX), also known as X-linked West syndrome, and Rett syndrome (RTT). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":18425583,"end":18653629,"strand":1,"description":"cyclin dependent kinase like 5 [Source:HGNC Symbol;Acc:HGNC:11411]"}, {"versioned_ensembl_gene_id":"ENSG00000250772.5","gene_symbol":"LINC01365","gene_name":"long intergenic non-protein coding RNA 1365 [Source:HGNC Symbol;Acc:HGNC:50603]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927007","summary":null,"start":119799089,"end":119804515,"strand":-1,"description":"long intergenic non-protein coding RNA 1365 [Source:HGNC Symbol;Acc:HGNC:50603]"}, {"versioned_ensembl_gene_id":"ENSG00000235497.5","gene_symbol":"AC012506.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23375229,"end":23381299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233340.1","gene_symbol":"AL139120.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112671812,"end":112677819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260152.2","gene_symbol":"AC113208.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75114261,"end":75114868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224843.6","gene_symbol":"LINC00240","gene_name":"long intergenic non-protein coding RNA 240 [Source:HGNC Symbol;Acc:HGNC:18772]","synonyms":"NCRNA00240,C6orf41,bA373D17.1","biotype":"lincRNA","ncbi_id":"100133205","summary":null,"start":26956992,"end":27023924,"strand":1,"description":"long intergenic non-protein coding RNA 240 [Source:HGNC Symbol;Acc:HGNC:18772]"}, {"versioned_ensembl_gene_id":"ENSG00000259065.1","gene_symbol":"AC005520.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73787360,"end":73803270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244661.1","gene_symbol":"TRBV12-1","gene_name":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]","synonyms":"TCRBV12S1,TRBV121,TCRBV8S4P","biotype":"TR_V_pseudogene","ncbi_id":"28579","summary":null,"start":142415224,"end":142415666,"strand":1,"description":"T-cell receptor beta variable 12-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12183]"}, {"versioned_ensembl_gene_id":"ENSG00000211717.3","gene_symbol":"TRBV10-1","gene_name":"T-cell receptor beta variable 10-1(gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12177]","synonyms":"TCRBV10S1,TRBV101,TCRBV12S2A1T,TCRBV12S2","biotype":"TR_V_gene","ncbi_id":"28585","summary":null,"start":142399860,"end":142400377,"strand":1,"description":"T-cell receptor beta variable 10-1(gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12177]"}, {"versioned_ensembl_gene_id":"ENSG00000232975.1","gene_symbol":"MTCO1P57","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:52315]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729155","summary":null,"start":68097737,"end":68098250,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:52315]"}, {"versioned_ensembl_gene_id":"ENSG00000236975.1","gene_symbol":"AL137793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":229092815,"end":229094905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059769.19","gene_symbol":"DNAJC25","gene_name":"DnaJ heat shock protein family (Hsp40) member C25 [Source:HGNC Symbol;Acc:HGNC:34187]","synonyms":"bA16L21.2.1","biotype":"protein_coding","ncbi_id":"548645","summary":null,"start":111631352,"end":111654351,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C25 [Source:HGNC Symbol;Acc:HGNC:34187]"}, {"versioned_ensembl_gene_id":"ENSG00000206310.8","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32250505,"end":32329363,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000163684.11","gene_symbol":"RPP14","gene_name":"ribonuclease P/MRP subunit p14 [Source:HGNC Symbol;Acc:HGNC:30327]","synonyms":"P14","biotype":"protein_coding","ncbi_id":"11102","summary":"This gene encodes a subunit of ribonuclease P and has 3' to 5' exoribonuclease activity. Transcripts for this gene are bicistronic and include a conserved downstream open reading frame for the hydroxyacyl-thioester dehydratase type 2 (HTD2) gene. [provided by RefSeq, May 2017]","start":58306247,"end":58324695,"strand":1,"description":"ribonuclease P/MRP subunit p14 [Source:HGNC Symbol;Acc:HGNC:30327]"}, {"versioned_ensembl_gene_id":"ENSG00000181704.11","gene_symbol":"YIPF6","gene_name":"Yip1 domain family member 6 [Source:HGNC Symbol;Acc:HGNC:28304]","synonyms":"MGC21416,FinGER6","biotype":"protein_coding","ncbi_id":"286451","summary":null,"start":68498323,"end":68537285,"strand":1,"description":"Yip1 domain family member 6 [Source:HGNC Symbol;Acc:HGNC:28304]"}, {"versioned_ensembl_gene_id":"ENSG00000229687.2","gene_symbol":"AL049745.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53841547,"end":53841832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250274.1","gene_symbol":"AC034199.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170308701,"end":170312716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230841.2","gene_symbol":"RPL23AP15","gene_name":"ribosomal protein L23a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391175","summary":null,"start":228449163,"end":228449621,"strand":-1,"description":"ribosomal protein L23a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36486]"}, {"versioned_ensembl_gene_id":"ENSG00000271227.1","gene_symbol":"AL109918.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52688661,"end":52688998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268407.1","gene_symbol":"AC006115.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56793048,"end":56793249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281648.1","gene_symbol":"AC131097.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241844380,"end":241845036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143355.15","gene_symbol":"LHX9","gene_name":"LIM homeobox 9 [Source:HGNC Symbol;Acc:HGNC:14222]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56956","summary":"This gene encodes a member of the LIM homeobox gene family of developmentally expressed transcription factors. The encoded protein contains a homeodomain and two cysteine-rich zinc-binding LIM domains involved in protein-protein interactions. The protein is highly similar to a mouse protein that causes gonadal agenesis when inactivated, suggesting a role in gonadal development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":197911902,"end":197935478,"strand":1,"description":"LIM homeobox 9 [Source:HGNC Symbol;Acc:HGNC:14222]"}, {"versioned_ensembl_gene_id":"ENSG00000267658.1","gene_symbol":"AC099811.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42154600,"end":42155972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183389.5","gene_symbol":"OR56A4","gene_name":"olfactory receptor family 56 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14791]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120793","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5999445,"end":6006946,"strand":-1,"description":"olfactory receptor family 56 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14791]"}, {"versioned_ensembl_gene_id":"ENSG00000197951.8","gene_symbol":"ZNF71","gene_name":"zinc finger protein 71 [Source:HGNC Symbol;Acc:HGNC:13141]","synonyms":"EZFIT,Cos26","biotype":"protein_coding","ncbi_id":"58491","summary":null,"start":56595264,"end":56626481,"strand":1,"description":"zinc finger protein 71 [Source:HGNC Symbol;Acc:HGNC:13141]"}, {"versioned_ensembl_gene_id":"ENSG00000233829.1","gene_symbol":"AC017078.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46003942,"end":46004309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148826.8","gene_symbol":"NKX6-2","gene_name":"NK6 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:19321]","synonyms":"NKX6B,NKX6.1,GTX","biotype":"protein_coding","ncbi_id":"84504","summary":null,"start":132783179,"end":132786052,"strand":-1,"description":"NK6 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:19321]"}, {"versioned_ensembl_gene_id":"ENSG00000166160.9","gene_symbol":"OPN1MW2","gene_name":"opsin 1, medium wave sensitive 2 [Source:HGNC Symbol;Acc:HGNC:26952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728458","summary":"This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009]","start":154219756,"end":154233286,"strand":1,"description":"opsin 1, medium wave sensitive 2 [Source:HGNC Symbol;Acc:HGNC:26952]"}, {"versioned_ensembl_gene_id":"ENSG00000226836.5","gene_symbol":"AC018437.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15943127,"end":15943532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105737.9","gene_symbol":"GRIK5","gene_name":"glutamate ionotropic receptor kainate type subunit 5 [Source:HGNC Symbol;Acc:HGNC:4583]","synonyms":"KA2,GRIK2,GluK5","biotype":"protein_coding","ncbi_id":"2901","summary":"This gene encodes a protein that belongs to the glutamate-gated ionic channel family. Glutamate functions as the major excitatory neurotransmitter in the central nervous system through activation of ligand-gated ion channels and G protein-coupled membrane receptors. The protein encoded by this gene forms functional heteromeric kainate-preferring ionic channels with the subunits encoded by related gene family members. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":41998321,"end":42069498,"strand":-1,"description":"glutamate ionotropic receptor kainate type subunit 5 [Source:HGNC Symbol;Acc:HGNC:4583]"}, {"versioned_ensembl_gene_id":"ENSG00000282085.1","gene_symbol":"AC105227.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50318420,"end":50319024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249729.2","gene_symbol":"AC093755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44840380,"end":44841402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004139.13","gene_symbol":"SARM1","gene_name":"sterile alpha and TIR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:17074]","synonyms":"SARM,SAMD2,KIAA0524","biotype":"protein_coding","ncbi_id":"23098","summary":null,"start":28364356,"end":28404049,"strand":1,"description":"sterile alpha and TIR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:17074]"}, {"versioned_ensembl_gene_id":"ENSG00000260357.1","gene_symbol":"DNM1P34","gene_name":"dynamin 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35181]","synonyms":"DNM1DN8@,DNM1DN8-5,DNM1DN8-1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729809","summary":null,"start":75299953,"end":75302965,"strand":-1,"description":"dynamin 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35181]"}, {"versioned_ensembl_gene_id":"ENSG00000206228.4","gene_symbol":"HNRNPA1P4","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32234]","synonyms":"HNRPA1P4","biotype":"processed_pseudogene","ncbi_id":"389674","summary":null,"start":82291624,"end":82292379,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32234]"}, {"versioned_ensembl_gene_id":"ENSG00000184478.7","gene_symbol":"OR56A3","gene_name":"olfactory receptor family 56 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:14786]","synonyms":"OR56A6,OR56A3P","biotype":"protein_coding","ncbi_id":"390083","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5938751,"end":5951347,"strand":1,"description":"olfactory receptor family 56 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:14786]"}, {"versioned_ensembl_gene_id":"ENSG00000270460.1","gene_symbol":"AC106900.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173811076,"end":173811392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272645.3","gene_symbol":"GTF2IP20","gene_name":"general transcription factor IIi pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51732]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441124","summary":null,"start":223951394,"end":223992594,"strand":-1,"description":"general transcription factor IIi pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51732]"}, {"versioned_ensembl_gene_id":"ENSG00000275099.2","gene_symbol":"GGNBP2","gene_name":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]","synonyms":"ZNF403,ZFP403,LZK1,FLJ22561,FLJ21230,DIF3,DIF-3","biotype":"protein_coding","ncbi_id":"79893","summary":null,"start":36545260,"end":36590811,"strand":1,"description":"gametogenetin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19357]"}, {"versioned_ensembl_gene_id":"ENSG00000166676.14","gene_symbol":"TVP23A","gene_name":"trans-golgi network vesicle protein 23 homolog A [Source:HGNC Symbol;Acc:HGNC:20398]","synonyms":"YDR084C,FAM18A","biotype":"protein_coding","ncbi_id":"780776","summary":"This gene encodes a membrane protein associated with the Golgi apparatus, which plays a crucial role in intracellular vesicular transport. The encoded protein is likely associated with the late (trans) Golgi compartments, which are involved in the delivery of secretory and membrane proteins to the endosome, lysosome or the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":10760919,"end":10818794,"strand":-1,"description":"trans-golgi network vesicle protein 23 homolog A [Source:HGNC Symbol;Acc:HGNC:20398]"}, {"versioned_ensembl_gene_id":"ENSG00000100124.14","gene_symbol":"ANKRD54","gene_name":"ankyrin repeat domain 54 [Source:HGNC Symbol;Acc:HGNC:25185]","synonyms":"LIAR","biotype":"protein_coding","ncbi_id":"129138","summary":null,"start":37830855,"end":37849327,"strand":-1,"description":"ankyrin repeat domain 54 [Source:HGNC Symbol;Acc:HGNC:25185]"}, {"versioned_ensembl_gene_id":"ENSG00000006652.13","gene_symbol":"IFRD1","gene_name":"interferon related developmental regulator 1 [Source:HGNC Symbol;Acc:HGNC:5456]","synonyms":"TIS7,PC4","biotype":"protein_coding","ncbi_id":"3475","summary":"This gene is an immediate early gene that encodes a protein related to interferon-gamma. This protein may function as a transcriptional co-activator/repressor that controls the growth and differentiation of specific cell types during embryonic development and tissue regeneration. Mutations in this gene are associated with sensory/motor neuropathy with ataxia. This gene may also be involved in modulating the pathogenesis of cystic fibrosis lung disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]","start":112422968,"end":112481017,"strand":1,"description":"interferon related developmental regulator 1 [Source:HGNC Symbol;Acc:HGNC:5456]"}, {"versioned_ensembl_gene_id":"ENSG00000255749.1","gene_symbol":"GNAI2P1","gene_name":"G protein subunit alpha i2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4386]","synonyms":"GNAI2L,GNAI2A","biotype":"processed_pseudogene","ncbi_id":"2772","summary":null,"start":14254912,"end":14255226,"strand":1,"description":"G protein subunit alpha i2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4386]"}, {"versioned_ensembl_gene_id":"ENSG00000198843.12","gene_symbol":"SELENOT","gene_name":"selenoprotein T [Source:HGNC Symbol;Acc:HGNC:18136]","synonyms":"SELT","biotype":"protein_coding","ncbi_id":"51714","summary":"This gene encodes a selenoprotein, containing a selenocysteine (Sec) residue at the active site. Sec is encoded by the UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is localized in the endoplasmic reticulum. It belongs to the SelWTH family that possesses a thioredoxin-like fold and a conserved CxxU (C is cysteine, U is Sec) motif found in several redox active proteins. Studies in mice indicate a crucial role for this gene in the protection of dopaminergic neurons against oxidative stress in Parkinson's disease, and in the control of glucose homeostasis in pancreatic beta-cells. Pseudogenes of this locus have been identified on chromosomes 9 and 5. [provided by RefSeq, Sep 2017]","start":150602875,"end":150630445,"strand":1,"description":"selenoprotein T [Source:HGNC Symbol;Acc:HGNC:18136]"}, {"versioned_ensembl_gene_id":"ENSG00000233023.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29747798,"end":29748218,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000280710.2","gene_symbol":"AL139035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99498524,"end":99501315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261529.1","gene_symbol":"AC100774.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25345633,"end":25347235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225455.3","gene_symbol":"TPI1P4","gene_name":"triosephosphate isomerase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38071]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728629","summary":null,"start":49016682,"end":49017154,"strand":-1,"description":"triosephosphate isomerase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38071]"}, {"versioned_ensembl_gene_id":"ENSG00000154124.4","gene_symbol":"OTULIN","gene_name":"OTU deubiquitinase with linear linkage specificity [Source:HGNC Symbol;Acc:HGNC:25118]","synonyms":"FLJ34884,FAM105B","biotype":"protein_coding","ncbi_id":"90268","summary":"This gene encodes a member of the peptidase C65 family of ubiquitin isopeptidases. Members of this family remove ubiquitin from proteins. The encoded enzyme specifically recognizes and removes M1(Met1)-linked, or linear, ubiquitin chains from protein substrates. Linear ubiquitin chains are known to regulate the NF-kappa B signaling pathway in the context of immunity and inflammation. Mutations in this gene cause a potentially fatal autoinflammatory syndrome in human patients. [provided by RefSeq, Sep 2016]","start":14664664,"end":14699711,"strand":1,"description":"OTU deubiquitinase with linear linkage specificity [Source:HGNC Symbol;Acc:HGNC:25118]"}, {"versioned_ensembl_gene_id":"ENSG00000256378.1","gene_symbol":"AC008011.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27935523,"end":27935749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270523.1","gene_symbol":"AC124303.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25130978,"end":25131337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102076.9","gene_symbol":"OPN1LW","gene_name":"opsin 1, long wave sensitive [Source:HGNC Symbol;Acc:HGNC:9936]","synonyms":"CBP,CBBM,RCP,COD5","biotype":"protein_coding","ncbi_id":"5956","summary":"This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness. [provided by RefSeq, Jul 2008]","start":154144224,"end":154159032,"strand":1,"description":"opsin 1, long wave sensitive [Source:HGNC Symbol;Acc:HGNC:9936]"}, {"versioned_ensembl_gene_id":"ENSG00000235126.1","gene_symbol":"AC128709.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197445061,"end":197458323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217809.1","gene_symbol":"FAT1P1","gene_name":"FAT atypical cadherin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16582]","synonyms":"dJ697P8.1","biotype":"processed_pseudogene","ncbi_id":"170513","summary":null,"start":10888582,"end":10889088,"strand":-1,"description":"FAT atypical cadherin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16582]"}, {"versioned_ensembl_gene_id":"ENSG00000254281.1","gene_symbol":"AP003354.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102978785,"end":103000184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124557.12","gene_symbol":"BTN1A1","gene_name":"butyrophilin subfamily 1 member A1 [Source:HGNC Symbol;Acc:HGNC:1135]","synonyms":"BTN1,BTN,BT","biotype":"protein_coding","ncbi_id":"696","summary":"Butyrophilin is the major protein associated with fat droplets in the milk. It is a member of the immunoglobulin superfamily. It may have a cell surface receptor function. The human butyrophilin gene is localized in the major histocompatibility complex (MHC) class I region of 6p and may have arisen relatively recently in evolution by the shuffling of exons between 2 ancestral gene families [provided by RefSeq, Jul 2008]","start":26501221,"end":26510422,"strand":1,"description":"butyrophilin subfamily 1 member A1 [Source:HGNC Symbol;Acc:HGNC:1135]"}, {"versioned_ensembl_gene_id":"ENSG00000266575.1","gene_symbol":"BOLA2P1","gene_name":"bolA family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51437]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652796","summary":null,"start":832238,"end":832469,"strand":1,"description":"bolA family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51437]"}, {"versioned_ensembl_gene_id":"ENSG00000105865.10","gene_symbol":"DUS4L","gene_name":"dihydrouridine synthase 4 like [Source:HGNC Symbol;Acc:HGNC:21517]","synonyms":"PP35,DUS4","biotype":"protein_coding","ncbi_id":"11062","summary":null,"start":107563484,"end":107578464,"strand":1,"description":"dihydrouridine synthase 4 like [Source:HGNC Symbol;Acc:HGNC:21517]"}, {"versioned_ensembl_gene_id":"ENSG00000233643.2","gene_symbol":"AC022398.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61781745,"end":61821246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165476.13","gene_symbol":"REEP3","gene_name":"receptor accessory protein 3 [Source:HGNC Symbol;Acc:HGNC:23711]","synonyms":"Yip2b,C10orf74","biotype":"protein_coding","ncbi_id":"221035","summary":null,"start":63521363,"end":63625123,"strand":1,"description":"receptor accessory protein 3 [Source:HGNC Symbol;Acc:HGNC:23711]"}, {"versioned_ensembl_gene_id":"ENSG00000282560.1","gene_symbol":"IGHV3-63","gene_name":"immunoglobulin heavy variable 3-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5616]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28415","summary":null,"start":106676918,"end":106677362,"strand":-1,"description":"immunoglobulin heavy variable 3-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5616]"}, {"versioned_ensembl_gene_id":"ENSG00000187764.11","gene_symbol":"SEMA4D","gene_name":"semaphorin 4D [Source:HGNC Symbol;Acc:HGNC:10732]","synonyms":"SEMAJ,FLJ39737,coll-4,CD100,C9orf164","biotype":"protein_coding","ncbi_id":"10507","summary":null,"start":89360787,"end":89498130,"strand":-1,"description":"semaphorin 4D [Source:HGNC Symbol;Acc:HGNC:10732]"}, {"versioned_ensembl_gene_id":"ENSG00000248127.1","gene_symbol":"AC026774.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76081946,"end":76084186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047579.19","gene_symbol":"DTNBP1","gene_name":"dystrobrevin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17328]","synonyms":"My031,HPS7,Dysbindin,DBND,BLOC1S8","biotype":"protein_coding","ncbi_id":"84062","summary":"This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. A similar protein in mouse is a component of a protein complex termed biogenesis of lysosome-related organelles complex 1 (BLOC-1), and binds to alpha- and beta-dystrobrevins, which are components of the dystrophin-associated protein complex (DPC). Mutations in this gene are associated with Hermansky-Pudlak syndrome type 7. This gene may also be associated with schizophrenia. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":15522801,"end":15663058,"strand":-1,"description":"dystrobrevin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17328]"}, {"versioned_ensembl_gene_id":"ENSG00000251668.2","gene_symbol":"AC113404.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76170930,"end":76171106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254893.6","gene_symbol":"AC113404.3","gene_name":null,"synonyms":null,"biotype":"translated_processed_pseudogene","ncbi_id":null,"summary":null,"start":76173629,"end":76174183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232451.1","gene_symbol":"AC018467.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23018125,"end":23199056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109079.9","gene_symbol":"TNFAIP1","gene_name":"TNF alpha induced protein 1 [Source:HGNC Symbol;Acc:HGNC:11894]","synonyms":"MGC2317,EDP1,BTBD34,B61,B12","biotype":"protein_coding","ncbi_id":"7126","summary":"This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. Studies of a similar gene in mouse suggest that the expression of this gene is developmentally regulated in a tissue-specific manner. [provided by RefSeq, Jul 2008]","start":28335602,"end":28347009,"strand":1,"description":"TNF alpha induced protein 1 [Source:HGNC Symbol;Acc:HGNC:11894]"}, {"versioned_ensembl_gene_id":"ENSG00000168158.3","gene_symbol":"OR2C1","gene_name":"olfactory receptor family 2 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8242]","synonyms":"OR2C2P,OLFmf3","biotype":"protein_coding","ncbi_id":"4993","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3355889,"end":3357294,"strand":1,"description":"olfactory receptor family 2 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8242]"}, {"versioned_ensembl_gene_id":"ENSG00000181004.9","gene_symbol":"BBS12","gene_name":"Bardet-Biedl syndrome 12 [Source:HGNC Symbol;Acc:HGNC:26648]","synonyms":"FLJ41559,FLJ35630,C4orf24","biotype":"protein_coding","ncbi_id":"166379","summary":"The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]","start":122732702,"end":122744943,"strand":1,"description":"Bardet-Biedl syndrome 12 [Source:HGNC Symbol;Acc:HGNC:26648]"}, {"versioned_ensembl_gene_id":"ENSG00000272420.1","gene_symbol":"AL513477.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2363061,"end":2363628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277080.1","gene_symbol":"AC010492.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54246700,"end":54247928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262107.1","gene_symbol":"MTND6P33","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52175]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075298","summary":null,"start":10719833,"end":10720015,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52175]"}, {"versioned_ensembl_gene_id":"ENSG00000240861.1","gene_symbol":"AC009153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74552251,"end":74552746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276566.1","gene_symbol":"IGKV1D-13","gene_name":"immunoglobulin kappa variable 1D-13 [Source:HGNC Symbol;Acc:HGNC:5747]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28902","summary":null,"start":90154073,"end":90154574,"strand":1,"description":"immunoglobulin kappa variable 1D-13 [Source:HGNC Symbol;Acc:HGNC:5747]"}, {"versioned_ensembl_gene_id":"ENSG00000214335.3","gene_symbol":"CTAGE16P","gene_name":"CTAGE family member 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:41967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341689","summary":null,"start":58528615,"end":58531026,"strand":1,"description":"CTAGE family member 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:41967]"}, {"versioned_ensembl_gene_id":"ENSG00000169083.16","gene_symbol":"AR","gene_name":"androgen receptor [Source:HGNC Symbol;Acc:HGNC:644]","synonyms":"HUMARA,DHTR,AIS,SMAX1,SBMA,NR3C4","biotype":"protein_coding","ncbi_id":"367","summary":"The androgen receptor gene is more than 90 kb long and codes for a protein that has 3 major functional domains: the N-terminal domain, DNA-binding domain, and androgen-binding domain. The protein functions as a steroid-hormone activated transcription factor. Upon binding the hormone ligand, the receptor dissociates from accessory proteins, translocates into the nucleus, dimerizes, and then stimulates transcription of androgen responsive genes. This gene contains 2 polymorphic trinucleotide repeat segments that encode polyglutamine and polyglycine tracts in the N-terminal transactivation domain of its protein. Expansion of the polyglutamine tract from the normal 9-34 repeats to the pathogenic 38-62 repeats causes spinal bulbar muscular atrophy (SBMA, also known as Kennedy's disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]","start":67544032,"end":67730619,"strand":1,"description":"androgen receptor [Source:HGNC Symbol;Acc:HGNC:644]"}, {"versioned_ensembl_gene_id":"ENSG00000277448.1","gene_symbol":"LINC02338","gene_name":"long intergenic non-protein coding RNA 2338 [Source:HGNC Symbol;Acc:HGNC:53258]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926897","summary":null,"start":58165827,"end":58209483,"strand":1,"description":"long intergenic non-protein coding RNA 2338 [Source:HGNC Symbol;Acc:HGNC:53258]"}, {"versioned_ensembl_gene_id":"ENSG00000163923.9","gene_symbol":"RPL39L","gene_name":"ribosomal protein L39 like [Source:HGNC Symbol;Acc:HGNC:17094]","synonyms":"RPL39L1","biotype":"protein_coding","ncbi_id":"116832","summary":"This gene encodes a protein sharing high sequence similarity with ribosomal protein L39. Although the name of this gene has been referred to as 'ribosomal protein L39' in the public databases, its official name is 'ribosomal protein L39-like'. It is not currently known whether the encoded protein is a functional ribosomal protein or whether it has evolved a function that is independent of the ribosome. [provided by RefSeq, Jul 2008]","start":187120948,"end":187180908,"strand":-1,"description":"ribosomal protein L39 like [Source:HGNC Symbol;Acc:HGNC:17094]"}, {"versioned_ensembl_gene_id":"ENSG00000005206.16","gene_symbol":"SPPL2B","gene_name":"signal peptide peptidase like 2B [Source:HGNC Symbol;Acc:HGNC:30627]","synonyms":"PSL1,KIAA1532,IMP4","biotype":"protein_coding","ncbi_id":"56928","summary":"This gene encodes a member of the GXGD family of aspartic proteases. The GXGD proteases are transmembrane proteins with two conserved catalytic motifs localized within the membrane-spanning regions. This enzyme localizes to endosomes, lysosomes, and the plasma membrane. It cleaves the transmembrane domain of tumor necrosis factor alpha to release the intracellular domain, which triggers cytokine expression in the innate and adaptive immunity pathways. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":2328615,"end":2354806,"strand":1,"description":"signal peptide peptidase like 2B [Source:HGNC Symbol;Acc:HGNC:30627]"}, {"versioned_ensembl_gene_id":"ENSG00000257668.1","gene_symbol":"AC084033.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57983795,"end":57984761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275316.3","gene_symbol":"IGHV3-49","gene_name":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28423","summary":null,"start":106581617,"end":106582158,"strand":-1,"description":"immunoglobulin heavy variable 3-49 [Source:HGNC Symbol;Acc:HGNC:5607]"}, {"versioned_ensembl_gene_id":"ENSG00000254008.1","gene_symbol":"LINC00051","gene_name":"long intergenic non-protein coding RNA 51 [Source:HGNC Symbol;Acc:HGNC:32028]","synonyms":"NCRNA00051,C8orf43","biotype":"antisense_RNA","ncbi_id":"619434","summary":null,"start":142198356,"end":142209003,"strand":1,"description":"long intergenic non-protein coding RNA 51 [Source:HGNC Symbol;Acc:HGNC:32028]"}, {"versioned_ensembl_gene_id":"ENSG00000244558.5","gene_symbol":"KCNK15-AS1","gene_name":"KCNK15 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49901]","synonyms":"RP11-445H22.4","biotype":"antisense_RNA","ncbi_id":"106144538","summary":null,"start":44694892,"end":44746021,"strand":-1,"description":"KCNK15 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49901]"}, {"versioned_ensembl_gene_id":"ENSG00000223663.2","gene_symbol":"NDUFB4P8","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45256]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075246","summary":null,"start":1378666,"end":1379032,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45256]"}, {"versioned_ensembl_gene_id":"ENSG00000188558.6","gene_symbol":"OR2G6","gene_name":"olfactory receptor family 2 subfamily G member 6 [Source:HGNC Symbol;Acc:HGNC:27019]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391211","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248508073,"end":248527337,"strand":1,"description":"olfactory receptor family 2 subfamily G member 6 [Source:HGNC Symbol;Acc:HGNC:27019]"}, {"versioned_ensembl_gene_id":"ENSG00000234998.1","gene_symbol":"AC244453.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121087528,"end":121116676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225214.1","gene_symbol":"AC079790.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152098328,"end":152109202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125863.18","gene_symbol":"MKKS","gene_name":"McKusick-Kaufman syndrome [Source:HGNC Symbol;Acc:HGNC:7108]","synonyms":"BBS6","biotype":"protein_coding","ncbi_id":"8195","summary":"This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family. The encoded protein is a centrosome-shuttling protein and plays an important role in cytokinesis. This protein also interacts with other type II chaperonin members to form a complex known as the BBSome, which involves ciliary membrane biogenesis. This protein is encoded by a downstream open reading frame (dORF). Several upstream open reading frames (uORFs) have been identified, which repress the translation of the dORF, and two of which can encode small mitochondrial membrane proteins. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 6, also known as McKusick-Kaufman syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":10401009,"end":10434222,"strand":-1,"description":"McKusick-Kaufman syndrome [Source:HGNC Symbol;Acc:HGNC:7108]"}, {"versioned_ensembl_gene_id":"ENSG00000223601.2","gene_symbol":"EBLN1","gene_name":"endogenous Bornavirus like nucleoprotein 1 [Source:HGNC Symbol;Acc:HGNC:39430]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340900","summary":null,"start":22208814,"end":22210021,"strand":-1,"description":"endogenous Bornavirus like nucleoprotein 1 [Source:HGNC Symbol;Acc:HGNC:39430]"}, {"versioned_ensembl_gene_id":"ENSG00000168803.14","gene_symbol":"ADAL","gene_name":"adenosine deaminase like [Source:HGNC Symbol;Acc:HGNC:31853]","synonyms":null,"biotype":"protein_coding","ncbi_id":"161823","summary":null,"start":43330674,"end":43354555,"strand":1,"description":"adenosine deaminase like [Source:HGNC Symbol;Acc:HGNC:31853]"}, {"versioned_ensembl_gene_id":"ENSG00000231211.2","gene_symbol":"RPL17P49","gene_name":"ribosomal protein L17 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:37009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271388","summary":null,"start":12395757,"end":12396167,"strand":-1,"description":"ribosomal protein L17 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:37009]"}, {"versioned_ensembl_gene_id":"ENSG00000151917.17","gene_symbol":"BEND6","gene_name":"BEN domain containing 6 [Source:HGNC Symbol;Acc:HGNC:20871]","synonyms":"FLJ30162,C6orf65,bA203B9.1","biotype":"protein_coding","ncbi_id":"221336","summary":null,"start":56955126,"end":57027342,"strand":1,"description":"BEN domain containing 6 [Source:HGNC Symbol;Acc:HGNC:20871]"}, {"versioned_ensembl_gene_id":"ENSG00000270094.1","gene_symbol":"AL670729.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228394290,"end":228396967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219790.3","gene_symbol":"OSTCP6","gene_name":"oligosaccharyltransferase complex subunit pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42868]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874387","summary":null,"start":56975606,"end":56976062,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42868]"}, {"versioned_ensembl_gene_id":"ENSG00000282520.1","gene_symbol":"IGHD3OR15-3A","gene_name":"immunoglobulin heavy diversity 3/OR15-3A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5500]","synonyms":"IGHD3OR153A,IGHD3/OR15-3A","biotype":"IG_D_gene","ncbi_id":"28331","summary":null,"start":20005905,"end":20005935,"strand":-1,"description":"immunoglobulin heavy diversity 3/OR15-3A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5500]"}, {"versioned_ensembl_gene_id":"ENSG00000237603.1","gene_symbol":"HMGB3P12","gene_name":"high mobility group box 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39304]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873898","summary":null,"start":26216322,"end":26216877,"strand":1,"description":"high mobility group box 3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39304]"}, {"versioned_ensembl_gene_id":"ENSG00000181991.15","gene_symbol":"MRPS11","gene_name":"mitochondrial ribosomal protein S11 [Source:HGNC Symbol;Acc:HGNC:14050]","synonyms":"HCC-2,FLJ23406,FLJ22512","biotype":"protein_coding","ncbi_id":"64963","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that contains a high level of sequence similarity with ribosomal protein S11P family members. A pseudogene corresponding to this gene is found on chromosome 20. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2016]","start":88467453,"end":88480773,"strand":1,"description":"mitochondrial ribosomal protein S11 [Source:HGNC Symbol;Acc:HGNC:14050]"}, {"versioned_ensembl_gene_id":"ENSG00000241244.1","gene_symbol":"IGKV1D-16","gene_name":"immunoglobulin kappa variable 1D-16 [Source:HGNC Symbol;Acc:HGNC:5748]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28901","summary":null,"start":90100236,"end":90100738,"strand":1,"description":"immunoglobulin kappa variable 1D-16 [Source:HGNC Symbol;Acc:HGNC:5748]"}, {"versioned_ensembl_gene_id":"ENSG00000115350.11","gene_symbol":"POLE4","gene_name":"DNA polymerase epsilon 4, accessory subunit [Source:HGNC Symbol;Acc:HGNC:18755]","synonyms":"p12","biotype":"protein_coding","ncbi_id":"56655","summary":"POLE4 is a histone-fold protein that interacts with other histone-fold proteins to bind DNA in a sequence-independent manner. These histone-fold protein dimers combine within larger enzymatic complexes for DNA transcription, replication, and packaging.[supplied by OMIM, Apr 2004]","start":74958492,"end":74970128,"strand":1,"description":"DNA polymerase epsilon 4, accessory subunit [Source:HGNC Symbol;Acc:HGNC:18755]"}, {"versioned_ensembl_gene_id":"ENSG00000138684.7","gene_symbol":"IL21","gene_name":"interleukin 21 [Source:HGNC Symbol;Acc:HGNC:6005]","synonyms":"Za11,IL-21","biotype":"protein_coding","ncbi_id":"59067","summary":"This gene encodes a member of the common-gamma chain family of cytokines with immunoregulatory activity. The encoded protein plays a role in both the innate and adaptive immune responses by inducing the differentiation, proliferation and activity of multiple target cells including macrophages, natural killer cells, B cells and cytotoxic T cells. Dysregulation of this gene plays a role in multiple immune-mediated diseases including lupus, psoriasis and chronic inflammatory diseases. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":122612628,"end":122621069,"strand":-1,"description":"interleukin 21 [Source:HGNC Symbol;Acc:HGNC:6005]"}, {"versioned_ensembl_gene_id":"ENSG00000134882.15","gene_symbol":"UBAC2","gene_name":"UBA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20486]","synonyms":"RP11-178C10.1,PHGDHL1,FLJ30548","biotype":"protein_coding","ncbi_id":"337867","summary":null,"start":99200774,"end":99386434,"strand":1,"description":"UBA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20486]"}, {"versioned_ensembl_gene_id":"ENSG00000235429.1","gene_symbol":"AC083875.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133315009,"end":133315413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100083.18","gene_symbol":"GGA1","gene_name":"golgi associated, gamma adaptin ear containing, ARF binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26088","summary":"This gene encodes a member of the Golgi-localized, gamma adaptin ear-containing, ARF-binding (GGA) protein family. Members of this family are ubiquitous coat proteins that regulate the trafficking of proteins between the trans-Golgi network and the lysosome. These proteins share an amino-terminal VHS domain which mediates sorting of the mannose 6-phosphate receptors at the trans-Golgi network. They also contain a carboxy-terminal region with homology to the ear domain of gamma-adaptins. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":37608475,"end":37633564,"strand":1,"description":"golgi associated, gamma adaptin ear containing, ARF binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17842]"}, {"versioned_ensembl_gene_id":"ENSG00000030110.12","gene_symbol":"BAK1","gene_name":"BCL2 antagonist/killer 1 [Source:HGNC Symbol;Acc:HGNC:949]","synonyms":"CDN1,BCL2L7,BAK","biotype":"protein_coding","ncbi_id":"578","summary":"The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form oligomers or heterodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. This protein localizes to mitochondria, and functions to induce apoptosis. It interacts with and accelerates the opening of the mitochondrial voltage-dependent anion channel, which leads to a loss in membrane potential and the release of cytochrome c. This protein also interacts with the tumor suppressor P53 after exposure to cell stress. [provided by RefSeq, Jul 2008]","start":33572547,"end":33580293,"strand":-1,"description":"BCL2 antagonist/killer 1 [Source:HGNC Symbol;Acc:HGNC:949]"}, {"versioned_ensembl_gene_id":"ENSG00000240159.1","gene_symbol":"AC079080.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184254509,"end":184255330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253678.1","gene_symbol":"AC104964.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10477491,"end":10479375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152464.14","gene_symbol":"RPP38","gene_name":"ribonuclease P/MRP subunit p38 [Source:HGNC Symbol;Acc:HGNC:30329]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10557","summary":null,"start":15097180,"end":15139818,"strand":1,"description":"ribonuclease P/MRP subunit p38 [Source:HGNC Symbol;Acc:HGNC:30329]"}, {"versioned_ensembl_gene_id":"ENSG00000255166.1","gene_symbol":"AC022616.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43247191,"end":43247410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279389.3","gene_symbol":"KIAA0355","gene_name":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9710","summary":null,"start":34261710,"end":34308123,"strand":1,"description":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]"}, {"versioned_ensembl_gene_id":"ENSG00000196862.9","gene_symbol":"RGPD4","gene_name":"RANBP2-like and GRIP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32417]","synonyms":"RGP4,DKFZp686P0288","biotype":"protein_coding","ncbi_id":"285190","summary":null,"start":107826937,"end":107890841,"strand":1,"description":"RANBP2-like and GRIP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:32417]"}, {"versioned_ensembl_gene_id":"ENSG00000253884.1","gene_symbol":"AC022616.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43246755,"end":43246935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241853.1","gene_symbol":"AC097484.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88163579,"end":88163967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235795.1","gene_symbol":"AC093157.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100995473,"end":100996260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136750.11","gene_symbol":"GAD2","gene_name":"glutamate decarboxylase 2 [Source:HGNC Symbol;Acc:HGNC:4093]","synonyms":"GAD65","biotype":"protein_coding","ncbi_id":"2572","summary":"This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantibody and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2008]","start":26216307,"end":26304558,"strand":1,"description":"glutamate decarboxylase 2 [Source:HGNC Symbol;Acc:HGNC:4093]"}, {"versioned_ensembl_gene_id":"ENSG00000259338.1","gene_symbol":"AC051619.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45215547,"end":45215943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088387.18","gene_symbol":"DOCK9","gene_name":"dedicator of cytokinesis 9 [Source:HGNC Symbol;Acc:HGNC:14132]","synonyms":"ZIZ1,KIAA1058","biotype":"protein_coding","ncbi_id":"23348","summary":null,"start":98793429,"end":99086625,"strand":-1,"description":"dedicator of cytokinesis 9 [Source:HGNC Symbol;Acc:HGNC:14132]"}, {"versioned_ensembl_gene_id":"ENSG00000250614.1","gene_symbol":"AC005522.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76474587,"end":76478856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173531.15","gene_symbol":"MST1","gene_name":"macrophage stimulating 1 [Source:HGNC Symbol;Acc:HGNC:7380]","synonyms":"NF15S2,MSP,HGFL,DNF15S2,D3F15S2","biotype":"protein_coding","ncbi_id":"4485","summary":"The protein encoded by this gene contains four kringle domains and a serine protease domain, similar to that found in hepatic growth factor. Despite the presence of the serine protease domain, the encoded protein may not have any proteolytic activity. The receptor for this protein is RON tyrosine kinase, which upon activation stimulates ciliary motility of ciliated epithelial lung cells. This protein is secreted and cleaved to form an alpha chain and a beta chain bridged by disulfide bonds. [provided by RefSeq, Jan 2010]","start":49683947,"end":49689501,"strand":-1,"description":"macrophage stimulating 1 [Source:HGNC Symbol;Acc:HGNC:7380]"}, {"versioned_ensembl_gene_id":"ENSG00000104731.13","gene_symbol":"KLHDC4","gene_name":"kelch domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25272]","synonyms":"DKFZp434G0522","biotype":"protein_coding","ncbi_id":"54758","summary":null,"start":87696485,"end":87765992,"strand":-1,"description":"kelch domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25272]"}, {"versioned_ensembl_gene_id":"ENSG00000158062.20","gene_symbol":"UBXN11","gene_name":"UBX domain protein 11 [Source:HGNC Symbol;Acc:HGNC:30600]","synonyms":"UBXD5,SOCI,SOC","biotype":"protein_coding","ncbi_id":"91544","summary":"This gene encodes a protein with a divergent C-terminal UBX domain. The homologous protein in the rat interacts with members of the Rnd subfamily of Rho GTPases at the cell periphery through its C-terminal region. It also interacts with several heterotrimeric G proteins through their G-alpha subunits and promotes Rho GTPase activation. It is proposed to serve a bidirectional role in the promotion and inhibition of Rho activity through upstream signaling pathways. The 3' coding sequence of this gene contains a polymoprhic region of 24 nt tandem repeats. Several transcripts containing between 1.5 and five repeat units have been reported. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":26281328,"end":26318363,"strand":-1,"description":"UBX domain protein 11 [Source:HGNC Symbol;Acc:HGNC:30600]"}, {"versioned_ensembl_gene_id":"ENSG00000282139.1","gene_symbol":"IGHVIII-5-2","gene_name":"immunoglobulin heavy variable (III)-5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5703]","synonyms":"IGHV(III)-5-2","biotype":"IG_V_pseudogene","ncbi_id":"28353","summary":null,"start":106046371,"end":106046631,"strand":-1,"description":"immunoglobulin heavy variable (III)-5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5703]"}, {"versioned_ensembl_gene_id":"ENSG00000279807.1","gene_symbol":"AC011472.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":11208195,"end":11208702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154118.12","gene_symbol":"JPH3","gene_name":"junctophilin 3 [Source:HGNC Symbol;Acc:HGNC:14203]","synonyms":"JP-3,HDL2,CAGL237,TNRC22,JP3","biotype":"protein_coding","ncbi_id":"57338","summary":"Junctional complexes between the plasma membrane and endoplasmic/sarcoplasmic reticulum are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. The protein encoded by this gene is a component of junctional complexes and is composed of a C-terminal hydrophobic segment spanning the endoplasmic/sarcoplasmic reticulum membrane and a remaining cytoplasmic domain that shows specific affinity for the plasma membrane. CAG/CTG repeat expansion from normally 6-28 repeats to 40-59 repeats in the 3' UTR of this gene have been associated with Huntington disease-like 2 (HDL2). This gene is a member of the junctophilin gene family. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jul 2016]","start":87601835,"end":87698156,"strand":1,"description":"junctophilin 3 [Source:HGNC Symbol;Acc:HGNC:14203]"}, {"versioned_ensembl_gene_id":"ENSG00000236782.6","gene_symbol":"AL391650.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":26169516,"end":26171821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214875.2","gene_symbol":"MED28P1","gene_name":"mediator complex subunit 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45078]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420207","summary":null,"start":68991137,"end":68991707,"strand":1,"description":"mediator complex subunit 28 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45078]"}, {"versioned_ensembl_gene_id":"ENSG00000215717.5","gene_symbol":"TMEM167B","gene_name":"transmembrane protein 167B [Source:HGNC Symbol;Acc:HGNC:30187]","synonyms":"FLJ90710,C1orf119,AD-020","biotype":"protein_coding","ncbi_id":"56900","summary":null,"start":109089803,"end":109096934,"strand":1,"description":"transmembrane protein 167B [Source:HGNC Symbol;Acc:HGNC:30187]"}, {"versioned_ensembl_gene_id":"ENSG00000235677.1","gene_symbol":"NPM1P26","gene_name":"nucleophosmin 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:45205]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422313","summary":null,"start":96560185,"end":96560922,"strand":1,"description":"nucleophosmin 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:45205]"}, {"versioned_ensembl_gene_id":"ENSG00000259371.2","gene_symbol":"AL136295.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24120956,"end":24131829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189227.5","gene_symbol":"C15orf61","gene_name":"chromosome 15 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:34453]","synonyms":"LOC145853","biotype":"protein_coding","ncbi_id":"145853","summary":null,"start":67521068,"end":67530143,"strand":1,"description":"chromosome 15 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:34453]"}, {"versioned_ensembl_gene_id":"ENSG00000103313.12","gene_symbol":"MEFV","gene_name":"MEFV, pyrin innate immunity regulator [Source:HGNC Symbol;Acc:HGNC:6998]","synonyms":"MEF,FMF,TRIM20","biotype":"protein_coding","ncbi_id":"4210","summary":"This gene encodes a protein, also known as pyrin or marenostrin, that is an important modulator of innate immunity. Mutations in this gene are associated with Mediterranean fever, a hereditary periodic fever syndrome. [provided by RefSeq, Jul 2008]","start":3242028,"end":3256627,"strand":-1,"description":"MEFV, pyrin innate immunity regulator [Source:HGNC Symbol;Acc:HGNC:6998]"}, {"versioned_ensembl_gene_id":"ENSG00000225399.4","gene_symbol":"AC121247.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49260085,"end":49261316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125089.16","gene_symbol":"SH3TC1","gene_name":"SH3 domain and tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:26009]","synonyms":"FLJ20356","biotype":"protein_coding","ncbi_id":"54436","summary":null,"start":8182072,"end":8241803,"strand":1,"description":"SH3 domain and tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:26009]"}, {"versioned_ensembl_gene_id":"ENSG00000226011.1","gene_symbol":"OFD1P1Y","gene_name":"OFD1 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:23873]","synonyms":"OFDYP1,OFD1P1","biotype":"unprocessed_pseudogene","ncbi_id":"378009","summary":null,"start":17809807,"end":17825329,"strand":1,"description":"OFD1 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:23873]"}, {"versioned_ensembl_gene_id":"ENSG00000259202.1","gene_symbol":"AC012568.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67142734,"end":67146939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115866.10","gene_symbol":"DARS","gene_name":"aspartyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:2678]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1615","summary":"This gene encodes a member of a multienzyme complex that functions in mediating the attachment of amino acids to their cognate tRNAs. The encoded protein ligates L-aspartate to tRNA(Asp). Mutations in this gene have been found in patients showing hypomyelination with brainstem and spinal cord involvement and leg spasticity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":135906677,"end":135986100,"strand":-1,"description":"aspartyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:2678]"}, {"versioned_ensembl_gene_id":"ENSG00000169340.9","gene_symbol":"PDILT","gene_name":"protein disulfide isomerase like, testis expressed [Source:HGNC Symbol;Acc:HGNC:27338]","synonyms":"PDIA7","biotype":"protein_coding","ncbi_id":"204474","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has has an N-terminal ER-signal sequence, two thioredoxin (TRX) domains with non-classical Ser-Lys-Gln-Ser and Ser-Lys-Lys-Cys motifs, respectively, two TRX-like domains, and a C-terminal ER-retention sequence. The protein lacks oxidoreductase activity in vitro and probably functions as a chaperone. This gene's expression appears to be limited to the testis. [provided by RefSeq, Dec 2016]","start":20359170,"end":20404737,"strand":-1,"description":"protein disulfide isomerase like, testis expressed [Source:HGNC Symbol;Acc:HGNC:27338]"}, {"versioned_ensembl_gene_id":"ENSG00000115526.10","gene_symbol":"CHST10","gene_name":"carbohydrate sulfotransferase 10 [Source:HGNC Symbol;Acc:HGNC:19650]","synonyms":"HNK-1ST","biotype":"protein_coding","ncbi_id":"9486","summary":"This protein encoded by this gene transfers sulfate to the C-3 hydroxyl of terminal glucuronic acid of protein- and lipid-linked oligosaccharides. This protein was first identified as a sulfotransferase that acts on the human natural killer-1 (HNK-1) glycan; HNK-1 is a carbohydrate involved in neurodevelopment and synaptic plasticity.[provided by RefSeq, Feb 2011]","start":100391860,"end":100417656,"strand":-1,"description":"carbohydrate sulfotransferase 10 [Source:HGNC Symbol;Acc:HGNC:19650]"}, {"versioned_ensembl_gene_id":"ENSG00000204335.3","gene_symbol":"SP5","gene_name":"Sp5 transcription factor [Source:HGNC Symbol;Acc:HGNC:14529]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389058","summary":null,"start":170715351,"end":170718078,"strand":1,"description":"Sp5 transcription factor [Source:HGNC Symbol;Acc:HGNC:14529]"}, {"versioned_ensembl_gene_id":"ENSG00000124140.13","gene_symbol":"SLC12A5","gene_name":"solute carrier family 12 member 5 [Source:HGNC Symbol;Acc:HGNC:13818]","synonyms":"KIAA1176,KCC2","biotype":"protein_coding","ncbi_id":"57468","summary":"K-Cl cotransporters are proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The protein encoded by this gene is an integral membrane K-Cl cotransporter that can function in either a net efflux or influx pathway, depending on the chemical concentration gradients of potassium and chloride. The encoded protein can act as a homomultimer, or as a heteromultimer with other K-Cl cotransporters, to maintain chloride homeostasis in neurons. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Sep 2008]","start":46021690,"end":46060152,"strand":1,"description":"solute carrier family 12 member 5 [Source:HGNC Symbol;Acc:HGNC:13818]"}, {"versioned_ensembl_gene_id":"ENSG00000227435.1","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"IPP-2P,PPP1R2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32857101,"end":32857778,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000155659.14","gene_symbol":"VSIG4","gene_name":"V-set and immunoglobulin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:17032]","synonyms":"Z39IG","biotype":"protein_coding","ncbi_id":"11326","summary":"This gene encodes a v-set and immunoglobulin-domain containing protein that is structurally related to the B7 family of immune regulatory proteins. The encoded protein may be a negative regulator of T-cell responses. This protein is also a receptor for the complement component 3 fragments C3b and iC3b. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":66021738,"end":66040125,"strand":-1,"description":"V-set and immunoglobulin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:17032]"}, {"versioned_ensembl_gene_id":"ENSG00000227739.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30710059,"end":30715284,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000276403.1","gene_symbol":"AC105105.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58476191,"end":58477484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227063.5","gene_symbol":"RPL41P1","gene_name":"ribosomal protein L41 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10356]","synonyms":"RPL41L2","biotype":"processed_pseudogene","ncbi_id":"22971","summary":null,"start":21755270,"end":21755350,"strand":1,"description":"ribosomal protein L41 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10356]"}, {"versioned_ensembl_gene_id":"ENSG00000281862.1","gene_symbol":"FAM90A23P","gene_name":"family with sequence similarity 90 member A23, pseudogene [Source:HGNC Symbol;Acc:HGNC:32271]","synonyms":"FAM90A23","biotype":"unprocessed_pseudogene","ncbi_id":"645572","summary":null,"start":7571620,"end":7574629,"strand":-1,"description":"family with sequence similarity 90 member A23, pseudogene [Source:HGNC Symbol;Acc:HGNC:32271]"}, {"versioned_ensembl_gene_id":"ENSG00000138160.5","gene_symbol":"KIF11","gene_name":"kinesin family member 11 [Source:HGNC Symbol;Acc:HGNC:6388]","synonyms":"TRIP5,KNSL1,HKSP,Eg5","biotype":"protein_coding","ncbi_id":"3832","summary":"This gene encodes a motor protein that belongs to the kinesin-like protein family. Members of this protein family are known to be involved in various kinds of spindle dynamics. The function of this gene product includes chromosome positioning, centrosome separation and establishing a bipolar spindle during cell mitosis. [provided by RefSeq, Jul 2008]","start":92593286,"end":92655395,"strand":1,"description":"kinesin family member 11 [Source:HGNC Symbol;Acc:HGNC:6388]"}, {"versioned_ensembl_gene_id":"ENSG00000282108.1","gene_symbol":"IGHVIII-2-1","gene_name":"immunoglobulin heavy variable (III)-2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5695]","synonyms":"IGHV(III)-2-1","biotype":"IG_V_pseudogene","ncbi_id":"28355","summary":null,"start":106002305,"end":106002595,"strand":-1,"description":"immunoglobulin heavy variable (III)-2-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5695]"}, {"versioned_ensembl_gene_id":"ENSG00000074181.8","gene_symbol":"NOTCH3","gene_name":"notch 3 [Source:HGNC Symbol;Acc:HGNC:7883]","synonyms":"CADASIL,CASIL","biotype":"protein_coding","ncbi_id":"4854","summary":"This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]","start":15159038,"end":15200981,"strand":-1,"description":"notch 3 [Source:HGNC Symbol;Acc:HGNC:7883]"}, {"versioned_ensembl_gene_id":"ENSG00000120341.18","gene_symbol":"SEC16B","gene_name":"SEC16 homolog B, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:30301]","synonyms":"Sec16S,RGPR,PGPR-p117,LZTR2","biotype":"protein_coding","ncbi_id":"89866","summary":"SEC16B is a mammalian homolog of S. cerevisiae Sec16 that is required for organization of transitional endoplasmic reticulum (ER) sites and protein export (Bhattacharyya and Glick, 2007 [PubMed 17192411]).[supplied by OMIM, Jun 2009]","start":177923956,"end":177984303,"strand":-1,"description":"SEC16 homolog B, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:30301]"}, {"versioned_ensembl_gene_id":"ENSG00000282114.1","gene_symbol":"LINC00824","gene_name":"long intergenic non-protein coding RNA 824 [Source:HGNC Symbol;Acc:HGNC:50281]","synonyms":"LINC01263","biotype":"processed_transcript","ncbi_id":"101927774","summary":null,"start":128559028,"end":128564679,"strand":-1,"description":"long intergenic non-protein coding RNA 824 [Source:HGNC Symbol;Acc:HGNC:50281]"}, {"versioned_ensembl_gene_id":"ENSG00000240118.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32822113,"end":32857517,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000267251.2","gene_symbol":"AC139100.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80183680,"end":80202992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233833.1","gene_symbol":"ETF1P3","gene_name":"eukaryotic translation termination factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3480]","synonyms":"SUP45L4","biotype":"processed_pseudogene","ncbi_id":"100132121","summary":null,"start":65794345,"end":65795835,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3480]"}, {"versioned_ensembl_gene_id":"ENSG00000233010.1","gene_symbol":"RPEP4","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44523]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420665","summary":null,"start":29608900,"end":29609501,"strand":1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44523]"}, {"versioned_ensembl_gene_id":"ENSG00000277976.1","gene_symbol":"KRT18P40","gene_name":"keratin 18 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:33409]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390904","summary":null,"start":20967473,"end":20971556,"strand":1,"description":"keratin 18 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:33409]"}, {"versioned_ensembl_gene_id":"ENSG00000253817.1","gene_symbol":"AC120036.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47198032,"end":47198323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254348.1","gene_symbol":"AC120036.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47189305,"end":47189560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253502.1","gene_symbol":"ATP6V1G1P2","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29359]","synonyms":"ATP6V1GP2","biotype":"processed_pseudogene","ncbi_id":"100128541","summary":null,"start":47194002,"end":47194347,"strand":-1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29359]"}, {"versioned_ensembl_gene_id":"ENSG00000188873.4","gene_symbol":"AC120036.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47157118,"end":47157771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261357.1","gene_symbol":"AC099518.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19065991,"end":19066694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240443.1","gene_symbol":"RPS10P20","gene_name":"ribosomal protein S10 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35829]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271547","summary":null,"start":48487946,"end":48488408,"strand":1,"description":"ribosomal protein S10 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35829]"}, {"versioned_ensembl_gene_id":"ENSG00000104886.11","gene_symbol":"PLEKHJ1","gene_name":"pleckstrin homology domain containing J1 [Source:HGNC Symbol;Acc:HGNC:18211]","synonyms":"FLJ10297","biotype":"protein_coding","ncbi_id":"55111","summary":null,"start":2230084,"end":2237704,"strand":-1,"description":"pleckstrin homology domain containing J1 [Source:HGNC Symbol;Acc:HGNC:18211]"}, {"versioned_ensembl_gene_id":"ENSG00000229132.2","gene_symbol":"EIF4A1P10","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421533","summary":null,"start":92113246,"end":92114461,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37930]"}, {"versioned_ensembl_gene_id":"ENSG00000167186.10","gene_symbol":"COQ7","gene_name":"coenzyme Q7, hydroxylase [Source:HGNC Symbol;Acc:HGNC:2244]","synonyms":"CLK-1,CAT5","biotype":"protein_coding","ncbi_id":"10229","summary":"The protein encoded by this gene is similar to a mitochondrial di-iron containing hydroxylase in Saccharomyces cerevisiae that is involved with ubiquinone biosynthesis. Mutations in the yeast gene lead to slower development and longer life span. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2010]","start":19067599,"end":19080095,"strand":1,"description":"coenzyme Q7, hydroxylase [Source:HGNC Symbol;Acc:HGNC:2244]"}, {"versioned_ensembl_gene_id":"ENSG00000167193.7","gene_symbol":"CRK","gene_name":"CRK proto-oncogene, adaptor protein [Source:HGNC Symbol;Acc:HGNC:2362]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1398","summary":"This gene encodes a member of an adapter protein family that binds to several tyrosine-phosphorylated proteins. The product of this gene has several SH2 and SH3 domains (src-homology domains) and is involved in several signaling pathways, recruiting cytoplasmic proteins in the vicinity of tyrosine kinase through SH2-phosphotyrosine interaction. The N-terminal SH2 domain of this protein functions as a positive regulator of transformation whereas the C-terminal SH3 domain functions as a negative regulator of transformation. Two alternative transcripts encoding different isoforms with distinct biological activity have been described. [provided by RefSeq, Jul 2008]","start":1420689,"end":1463162,"strand":-1,"description":"CRK proto-oncogene, adaptor protein [Source:HGNC Symbol;Acc:HGNC:2362]"}, {"versioned_ensembl_gene_id":"ENSG00000270538.1","gene_symbol":"AC121247.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49252129,"end":49252264,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279591.1","gene_symbol":"AC002044.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73015047,"end":73016016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142867.12","gene_symbol":"BCL10","gene_name":"B-cell CLL/lymphoma 10 [Source:HGNC Symbol;Acc:HGNC:989]","synonyms":"mE10,CLAP,CIPER,CARMEN,c-E10","biotype":"protein_coding","ncbi_id":"8915","summary":"This gene was identified by its translocation in a case of mucosa-associated lymphoid tissue (MALT) lymphoma. The protein encoded by this gene contains a caspase recruitment domain (CARD), and has been shown to induce apoptosis and to activate NF-kappaB. This protein is reported to interact with other CARD domain containing proteins including CARD9, 10, 11 and 14, which are thought to function as upstream regulators in NF-kappaB signaling. This protein is found to form a complex with MALT1, a protein encoded by another gene known to be translocated in MALT lymphoma. MALT1 and this protein are thought to synergize in the activation of NF-kappaB, and the deregulation of either of them may contribute to the same pathogenetic process that leads to the malignancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":85266248,"end":85277090,"strand":-1,"description":"B-cell CLL/lymphoma 10 [Source:HGNC Symbol;Acc:HGNC:989]"}, {"versioned_ensembl_gene_id":"ENSG00000223705.9","gene_symbol":"NSUN5P1","gene_name":"NOP2/Sun RNA methyltransferase family member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19146]","synonyms":"NSUN5B,WBSCR20B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"155400","summary":"This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":75410322,"end":75416787,"strand":1,"description":"NOP2/Sun RNA methyltransferase family member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19146]"}, {"versioned_ensembl_gene_id":"ENSG00000177830.17","gene_symbol":"CHID1","gene_name":"chitinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28474]","synonyms":"MGC3234,FLJ42707","biotype":"protein_coding","ncbi_id":"66005","summary":null,"start":867860,"end":915058,"strand":-1,"description":"chitinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28474]"}, {"versioned_ensembl_gene_id":"ENSG00000224831.3","gene_symbol":"AC117395.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149982181,"end":149983308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239351.1","gene_symbol":"NPM1P29","gene_name":"nucleophosmin 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:45208]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422259","summary":null,"start":149938997,"end":149939799,"strand":-1,"description":"nucleophosmin 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:45208]"}, {"versioned_ensembl_gene_id":"ENSG00000282714.1","gene_symbol":"IGHD1-1","gene_name":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]","synonyms":"IGHD11","biotype":"IG_D_gene","ncbi_id":"28510","summary":null,"start":105920273,"end":105920289,"strand":-1,"description":"immunoglobulin heavy diversity 1-1 [Source:HGNC Symbol;Acc:HGNC:5482]"}, {"versioned_ensembl_gene_id":"ENSG00000276393.1","gene_symbol":"AC105429.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87467138,"end":87467654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128283.6","gene_symbol":"CDC42EP1","gene_name":"CDC42 effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17014]","synonyms":"MSE55,CEP1,Borg5","biotype":"protein_coding","ncbi_id":"11135","summary":"CDC42 is a member of the Rho GTPase family that regulates multiple cellular activities, including actin polymerization. The protein encoded by this gene is a CDC42 binding protein that mediates actin cytoskeleton reorganization at the plasma membrane. This protein is secreted and is primarily found in bone marrow. [provided by RefSeq, Jul 2008]","start":37560447,"end":37569405,"strand":1,"description":"CDC42 effector protein 1 [Source:HGNC Symbol;Acc:HGNC:17014]"}, {"versioned_ensembl_gene_id":"ENSG00000225434.2","gene_symbol":"LINC01504","gene_name":"long intergenic non-protein coding RNA 1504 [Source:HGNC Symbol;Acc:HGNC:51185]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507540","summary":null,"start":72305430,"end":72343210,"strand":1,"description":"long intergenic non-protein coding RNA 1504 [Source:HGNC Symbol;Acc:HGNC:51185]"}, {"versioned_ensembl_gene_id":"ENSG00000230330.1","gene_symbol":"HMGN2P3","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33566]","synonyms":"HMGN2L3","biotype":"processed_pseudogene","ncbi_id":"728632","summary":null,"start":26032539,"end":26032811,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33566]"}, {"versioned_ensembl_gene_id":"ENSG00000260255.1","gene_symbol":"AC093524.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25824710,"end":25826330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231024.1","gene_symbol":"AC092431.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69700192,"end":69713847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225039.1","gene_symbol":"LINC01058","gene_name":"long intergenic non-protein coding RNA 1058 [Source:HGNC Symbol;Acc:HGNC:49061]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103724387","summary":null,"start":30419519,"end":30422237,"strand":-1,"description":"long intergenic non-protein coding RNA 1058 [Source:HGNC Symbol;Acc:HGNC:49061]"}, {"versioned_ensembl_gene_id":"ENSG00000136141.14","gene_symbol":"LRCH1","gene_name":"leucine rich repeats and calponin homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20309]","synonyms":"KIAA1016,CHDC1","biotype":"protein_coding","ncbi_id":"23143","summary":"This gene encodes a protein with a leucine-rich repeat and a calponin homology domain. Polymorphism in this gene may be associated with susceptibililty to knee osteoarthritis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2010]","start":46553168,"end":46753040,"strand":1,"description":"leucine rich repeats and calponin homology domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20309]"}, {"versioned_ensembl_gene_id":"ENSG00000165568.17","gene_symbol":"AKR1E2","gene_name":"aldo-keto reductase family 1 member E2 [Source:HGNC Symbol;Acc:HGNC:23437]","synonyms":"MGC10612,AKRDC1,AKR1CL2","biotype":"protein_coding","ncbi_id":"83592","summary":"The protein encoded by this gene is a member of the aldo-keto reductase superfamily. Members in this family are characterized by their structure (evolutionarily highly conserved TIM barrel) and function (NAD(P)H-dependent oxido-reduction of carbonyl groups). Transcripts of this gene have been reported in specimens of human testis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":4786629,"end":4848062,"strand":1,"description":"aldo-keto reductase family 1 member E2 [Source:HGNC Symbol;Acc:HGNC:23437]"}, {"versioned_ensembl_gene_id":"ENSG00000235525.1","gene_symbol":"FTLP1","gene_name":"ferritin light chain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16547]","synonyms":"FTLP,bA465L10.3","biotype":"processed_pseudogene","ncbi_id":"170514","summary":null,"start":45975249,"end":45976075,"strand":-1,"description":"ferritin light chain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16547]"}, {"versioned_ensembl_gene_id":"ENSG00000238178.6","gene_symbol":"AC078993.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16152941,"end":16170869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182798.10","gene_symbol":"MAGEB17","gene_name":"MAGE family member B17 [Source:HGNC Symbol;Acc:HGNC:17418]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645864","summary":null,"start":16167481,"end":16171464,"strand":1,"description":"MAGE family member B17 [Source:HGNC Symbol;Acc:HGNC:17418]"}, {"versioned_ensembl_gene_id":"ENSG00000095777.14","gene_symbol":"MYO3A","gene_name":"myosin IIIA [Source:HGNC Symbol;Acc:HGNC:7601]","synonyms":"DFNB30","biotype":"protein_coding","ncbi_id":"53904","summary":"The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008]","start":25934267,"end":26212527,"strand":1,"description":"myosin IIIA [Source:HGNC Symbol;Acc:HGNC:7601]"}, {"versioned_ensembl_gene_id":"ENSG00000133028.10","gene_symbol":"SCO1","gene_name":"SCO1, cytochrome c oxidase assembly protein [Source:HGNC Symbol;Acc:HGNC:10603]","synonyms":"SCOD1","biotype":"protein_coding","ncbi_id":"6341","summary":"Mammalian cytochrome c oxidase (COX) catalyzes the transfer of reducing equivalents from cytochrome c to molecular oxygen and pumps protons across the inner mitochondrial membrane. In yeast, 2 related COX assembly genes, SCO1 and SCO2 (synthesis of cytochrome c oxidase), enable subunits 1 and 2 to be incorporated into the holoprotein. This gene is the human homolog to the yeast SCO1 gene. [provided by RefSeq, Jul 2008]","start":10672474,"end":10698375,"strand":-1,"description":"SCO1, cytochrome c oxidase assembly protein [Source:HGNC Symbol;Acc:HGNC:10603]"}, {"versioned_ensembl_gene_id":"ENSG00000241464.3","gene_symbol":"RPL39P38","gene_name":"ribosomal protein L39 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271529","summary":null,"start":18285343,"end":18285495,"strand":-1,"description":"ribosomal protein L39 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36935]"}, {"versioned_ensembl_gene_id":"ENSG00000259234.5","gene_symbol":"ANKRD34C-AS1","gene_name":"ANKRD34C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48618]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729911","summary":null,"start":79191707,"end":79283945,"strand":-1,"description":"ANKRD34C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48618]"}, {"versioned_ensembl_gene_id":"ENSG00000272551.1","gene_symbol":"AC017048.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176611437,"end":176612249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231094.8","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"SEEK1,C6orf16","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31159671,"end":31184970,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000217261.4","gene_symbol":"POM121L4P","gene_name":"POM121 transmembrane nucleoporin like 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:19326]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"266697","summary":null,"start":20689929,"end":20698938,"strand":1,"description":"POM121 transmembrane nucleoporin like 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:19326]"}, {"versioned_ensembl_gene_id":"ENSG00000257473.7","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32565603,"end":32671108,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000270937.1","gene_symbol":"AL033381.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1026494,"end":1027225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176515.1","gene_symbol":"AL033381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1079929,"end":1104946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229731.1","gene_symbol":"AC107613.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27811885,"end":27812902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140948.11","gene_symbol":"ZCCHC14","gene_name":"zinc finger CCHC-type containing 14 [Source:HGNC Symbol;Acc:HGNC:24134]","synonyms":"BDG29,MGC14139","biotype":"protein_coding","ncbi_id":"23174","summary":null,"start":87406246,"end":87492045,"strand":-1,"description":"zinc finger CCHC-type containing 14 [Source:HGNC Symbol;Acc:HGNC:24134]"}, {"versioned_ensembl_gene_id":"ENSG00000234064.1","gene_symbol":"PRAMEF29P","gene_name":"PRAME family member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:51891]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729356","summary":null,"start":12926162,"end":12928253,"strand":1,"description":"PRAME family member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:51891]"}, {"versioned_ensembl_gene_id":"ENSG00000153779.10","gene_symbol":"TGIF2LX","gene_name":"TGFB induced factor homeobox 2 like, X-linked [Source:HGNC Symbol;Acc:HGNC:18570]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90316","summary":"This gene encodes a member of the TALE/TGIF homeobox family of transcription factors. Testis-specific expression suggests that this gene may play a role in spermatogenesis. A homolog of this gene lies within the male specific region of chromosome Y, in a block of sequence that is thought to be the result of a large X-to-Y transposition. [provided by RefSeq, Jul 2008]","start":89921882,"end":89922883,"strand":1,"description":"TGFB induced factor homeobox 2 like, X-linked [Source:HGNC Symbol;Acc:HGNC:18570]"}, {"versioned_ensembl_gene_id":"ENSG00000224065.2","gene_symbol":"SRIP2","gene_name":"sorcin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499485","summary":null,"start":89367435,"end":89367600,"strand":-1,"description":"sorcin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38734]"}, {"versioned_ensembl_gene_id":"ENSG00000235758.9","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32244640,"end":32254524,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000283547.1","gene_symbol":"AC099654.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57167200,"end":57167880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228945.3","gene_symbol":"CLUHP2","gene_name":"clustered mitochondria homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38453]","synonyms":"KIAA0664P2,KIAA0664L2","biotype":"unprocessed_pseudogene","ncbi_id":"100418709","summary":null,"start":18280178,"end":18284761,"strand":1,"description":"clustered mitochondria homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38453]"}, {"versioned_ensembl_gene_id":"ENSG00000213981.8","gene_symbol":"AC007277.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170640374,"end":170695374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241679.2","gene_symbol":"AC018450.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143123362,"end":143131893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236396.8","gene_symbol":"SLC35G4","gene_name":"solute carrier family 35 member G4 [Source:HGNC Symbol;Acc:HGNC:31043]","synonyms":"SLC35G4P,AMAC1L1","biotype":"protein_coding","ncbi_id":"646000","summary":null,"start":11609596,"end":11610612,"strand":1,"description":"solute carrier family 35 member G4 [Source:HGNC Symbol;Acc:HGNC:31043]"}, {"versioned_ensembl_gene_id":"ENSG00000282396.1","gene_symbol":"IGHD3-22","gene_name":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]","synonyms":"IGHD322","biotype":"IG_D_gene","ncbi_id":"28497","summary":null,"start":105886802,"end":105886832,"strand":-1,"description":"immunoglobulin heavy diversity 3-22 [Source:HGNC Symbol;Acc:HGNC:5497]"}, {"versioned_ensembl_gene_id":"ENSG00000167528.12","gene_symbol":"ZNF641","gene_name":"zinc finger protein 641 [Source:HGNC Symbol;Acc:HGNC:31834]","synonyms":"FLJ31295","biotype":"protein_coding","ncbi_id":"121274","summary":null,"start":48337180,"end":48351414,"strand":-1,"description":"zinc finger protein 641 [Source:HGNC Symbol;Acc:HGNC:31834]"}, {"versioned_ensembl_gene_id":"ENSG00000198060.9","gene_symbol":"MARCH5","gene_name":"membrane associated ring-CH-type finger 5 [Source:HGNC Symbol;Acc:HGNC:26025]","synonyms":"RNF153,MITOL,MARCH-V,FLJ20445","biotype":"protein_coding","ncbi_id":"54708","summary":"MARCH5 is a ubiquitin ligase of the mitochondrial outer membrane that plays a role in the control of mitochondrial morphology by regulating mitofusin-2 (MFN2; MIM 608507) and DRP1 (DNM1L; MIM 603850) (Nakamura et al., 2006 [PubMed 16936636]).[supplied by OMIM, Mar 2008]","start":92291163,"end":92353964,"strand":1,"description":"membrane associated ring-CH-type finger 5 [Source:HGNC Symbol;Acc:HGNC:26025]"}, {"versioned_ensembl_gene_id":"ENSG00000236063.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"D6S82E,BAT5,NG26","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31763228,"end":31779696,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000270893.1","gene_symbol":"AC008277.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159444117,"end":159444913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232805.1","gene_symbol":"NIP7P1","gene_name":"NIP7, nucleolar pre-rRNA processing protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45180]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389997","summary":null,"start":93106872,"end":93107383,"strand":-1,"description":"NIP7, nucleolar pre-rRNA processing protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45180]"}, {"versioned_ensembl_gene_id":"ENSG00000173239.13","gene_symbol":"LIPM","gene_name":"lipase family member M [Source:HGNC Symbol;Acc:HGNC:23455]","synonyms":"bA304I5.1,LIPL3","biotype":"protein_coding","ncbi_id":"340654","summary":null,"start":88802730,"end":88820546,"strand":1,"description":"lipase family member M [Source:HGNC Symbol;Acc:HGNC:23455]"}, {"versioned_ensembl_gene_id":"ENSG00000231388.1","gene_symbol":"AC079178.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26496936,"end":26505603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271161.1","gene_symbol":"BOLA2P2","gene_name":"bolA family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51438]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106480322","summary":null,"start":47499841,"end":47500407,"strand":1,"description":"bolA family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51438]"}, {"versioned_ensembl_gene_id":"ENSG00000257657.2","gene_symbol":"AC079950.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45481871,"end":45610620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111321.10","gene_symbol":"LTBR","gene_name":"lymphotoxin beta receptor [Source:HGNC Symbol;Acc:HGNC:6718]","synonyms":"TNFRSF3,TNFR2-RP,TNFR-RP,TNF-R-III,TNFCR,D12S370","biotype":"protein_coding","ncbi_id":"4055","summary":"This gene encodes a member of the tumor necrosis factor receptor superfamily. The major ligands of this receptor include lymphotoxin alpha/beta and tumor necrosis factor ligand superfamily member 14. The encoded protein plays a role in signalling during the development of lymphoid and other organs, lipid metabolism, immune response, and programmed cell death. Activity of this receptor has also been linked to carcinogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2012]","start":6375045,"end":6391571,"strand":1,"description":"lymphotoxin beta receptor [Source:HGNC Symbol;Acc:HGNC:6718]"}, {"versioned_ensembl_gene_id":"ENSG00000245910.8","gene_symbol":"SNHG6","gene_name":"small nucleolar RNA host gene 6 [Source:HGNC Symbol;Acc:HGNC:32965]","synonyms":"U87HG,NCRNA00058,HBII-276HG","biotype":"processed_transcript","ncbi_id":"641638","summary":null,"start":66921684,"end":66926398,"strand":-1,"description":"small nucleolar RNA host gene 6 [Source:HGNC Symbol;Acc:HGNC:32965]"}, {"versioned_ensembl_gene_id":"ENSG00000198286.9","gene_symbol":"CARD11","gene_name":"caspase recruitment domain family member 11 [Source:HGNC Symbol;Acc:HGNC:16393]","synonyms":"CARMA1,BIMP3","biotype":"protein_coding","ncbi_id":"84433","summary":"The protein encoded by this gene belongs to the membrane-associated guanylate kinase (MAGUK) family, a class of proteins that functions as molecular scaffolds for the assembly of multiprotein complexes at specialized regions of the plasma membrane. This protein is also a member of the CARD protein family, which is defined by carrying a characteristic caspase-associated recruitment domain (CARD). This protein has a domain structure similar to that of CARD14 protein. The CARD domains of both proteins have been shown to specifically interact with BCL10, a protein known to function as a positive regulator of cell apoptosis and NF-kappaB activation. When expressed in cells, this protein activated NF-kappaB and induced the phosphorylation of BCL10. [provided by RefSeq, Jul 2008]","start":2906141,"end":3043945,"strand":-1,"description":"caspase recruitment domain family member 11 [Source:HGNC Symbol;Acc:HGNC:16393]"}, {"versioned_ensembl_gene_id":"ENSG00000182552.14","gene_symbol":"RWDD4","gene_name":"RWD domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23750]","synonyms":"RWDD4A,MGC10198,FAM28A","biotype":"protein_coding","ncbi_id":"201965","summary":null,"start":183639635,"end":183659225,"strand":-1,"description":"RWD domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23750]"}, {"versioned_ensembl_gene_id":"ENSG00000248079.2","gene_symbol":"DPH6-AS1","gene_name":"DPH6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44147]","synonyms":"ATPBD4-AS1","biotype":"lincRNA","ncbi_id":"100507466","summary":null,"start":35546195,"end":35859001,"strand":1,"description":"DPH6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44147]"}, {"versioned_ensembl_gene_id":"ENSG00000233843.1","gene_symbol":"CYCSP48","gene_name":"cytochrome c, somatic pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:23942]","synonyms":"HCP48","biotype":"processed_pseudogene","ncbi_id":"360188","summary":null,"start":26400611,"end":26401230,"strand":1,"description":"cytochrome c, somatic pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:23942]"}, {"versioned_ensembl_gene_id":"ENSG00000278503.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54778013,"end":54792334,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000224685.1","gene_symbol":"AC099670.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100651947,"end":100652267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236060.2","gene_symbol":"HSPB1P1","gene_name":"heat shock protein family B (small) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5251]","synonyms":"HSPBL2","biotype":"processed_pseudogene","ncbi_id":"653553","summary":null,"start":72007881,"end":72008136,"strand":-1,"description":"heat shock protein family B (small) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5251]"}, {"versioned_ensembl_gene_id":"ENSG00000237558.1","gene_symbol":"CDY7P","gene_name":"chromodomain Y-linked 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:23854]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386731","summary":null,"start":17951589,"end":17953500,"strand":1,"description":"chromodomain Y-linked 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:23854]"}, {"versioned_ensembl_gene_id":"ENSG00000274410.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54746721,"end":54761251,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000173638.18","gene_symbol":"SLC19A1","gene_name":"solute carrier family 19 member 1 [Source:HGNC Symbol;Acc:HGNC:10937]","synonyms":"RFC1,FOLT","biotype":"protein_coding","ncbi_id":"6573","summary":"The membrane protein encoded by this gene is a transporter of folate and is involved in the regulation of intracellular concentrations of folate. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]","start":45493572,"end":45544411,"strand":-1,"description":"solute carrier family 19 member 1 [Source:HGNC Symbol;Acc:HGNC:10937]"}, {"versioned_ensembl_gene_id":"ENSG00000253313.5","gene_symbol":"C1orf210","gene_name":"chromosome 1 open reading frame 210 [Source:HGNC Symbol;Acc:HGNC:28755]","synonyms":"MGC52423","biotype":"protein_coding","ncbi_id":"149466","summary":null,"start":43281883,"end":43285617,"strand":-1,"description":"chromosome 1 open reading frame 210 [Source:HGNC Symbol;Acc:HGNC:28755]"}, {"versioned_ensembl_gene_id":"ENSG00000189166.6","gene_symbol":"TNRC18P3","gene_name":"trinucleotide repeat containing 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34015]","synonyms":"TNRC18C","biotype":"unprocessed_pseudogene","ncbi_id":"340221","summary":null,"start":56991888,"end":57009149,"strand":1,"description":"trinucleotide repeat containing 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34015]"}, {"versioned_ensembl_gene_id":"ENSG00000282619.1","gene_symbol":"AF186192.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144703585,"end":144711749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267399.1","gene_symbol":"AC006305.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56061109,"end":56063078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237108.1","gene_symbol":"CR759964.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31094157,"end":31098956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279703.1","gene_symbol":"AC017037.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":157818101,"end":157818572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267732.1","gene_symbol":"AC006305.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56138612,"end":56143221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249627.1","gene_symbol":"AC017037.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157815010,"end":157815480,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255559.1","gene_symbol":"ZNF252P-AS1","gene_name":"ZNF252P antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27821]","synonyms":"C8orf77","biotype":"antisense_RNA","ncbi_id":"286103","summary":null,"start":145002811,"end":145006046,"strand":1,"description":"ZNF252P antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27821]"}, {"versioned_ensembl_gene_id":"ENSG00000265091.5","gene_symbol":"AP001496.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5232876,"end":5238526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215277.8","gene_symbol":"RNF212B","gene_name":"ring finger protein 212B [Source:HGNC Symbol;Acc:HGNC:20438]","synonyms":"C14orf164","biotype":"protein_coding","ncbi_id":"100507650","summary":null,"start":23185316,"end":23273477,"strand":1,"description":"ring finger protein 212B [Source:HGNC Symbol;Acc:HGNC:20438]"}, {"versioned_ensembl_gene_id":"ENSG00000214344.4","gene_symbol":"OR4F13P","gene_name":"olfactory receptor family 4 subfamily F member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15076]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390651","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101842119,"end":101850324,"strand":1,"description":"olfactory receptor family 4 subfamily F member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15076]"}, {"versioned_ensembl_gene_id":"ENSG00000257604.1","gene_symbol":"AC027288.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79500119,"end":79500687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158156.7","gene_symbol":"XKR8","gene_name":"XK related 8 [Source:HGNC Symbol;Acc:HGNC:25508]","synonyms":"FLJ10307","biotype":"protein_coding","ncbi_id":"55113","summary":null,"start":27959462,"end":27968096,"strand":1,"description":"XK related 8 [Source:HGNC Symbol;Acc:HGNC:25508]"}, {"versioned_ensembl_gene_id":"ENSG00000273864.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54716447,"end":54721701,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000282113.1","gene_symbol":"LINC00976","gene_name":"long intergenic non-protein coding RNA 976 [Source:NCBI gene;Acc:106144608]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144608","summary":null,"start":128908170,"end":128924280,"strand":-1,"description":"long intergenic non-protein coding RNA 976 [Source:NCBI gene;Acc:106144608]"}, {"versioned_ensembl_gene_id":"ENSG00000122043.10","gene_symbol":"LINC00544","gene_name":"long intergenic non-protein coding RNA 544 [Source:HGNC Symbol;Acc:HGNC:43679]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440131","summary":null,"start":29935905,"end":29950488,"strand":1,"description":"long intergenic non-protein coding RNA 544 [Source:HGNC Symbol;Acc:HGNC:43679]"}, {"versioned_ensembl_gene_id":"ENSG00000262024.6","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"AR1,SPBP","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42147859,"end":42203293,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000105137.12","gene_symbol":"SYDE1","gene_name":"synapse defective Rho GTPase homolog 1 [Source:HGNC Symbol;Acc:HGNC:25824]","synonyms":"SYD1,FLJ13511,7h3","biotype":"protein_coding","ncbi_id":"85360","summary":"The protein encoded by this gene is a Rho GTPase-activating protein highly expressed in placenta. The encoded protein is involved in cytoskeletal remodeling and trophoblast cell migration. Decreased expression of this gene has been associated with intrauterine growth restriction (IUGR). [provided by RefSeq, Feb 2017]","start":15107403,"end":15114988,"strand":1,"description":"synapse defective Rho GTPase homolog 1 [Source:HGNC Symbol;Acc:HGNC:25824]"}, {"versioned_ensembl_gene_id":"ENSG00000183977.13","gene_symbol":"PP2D1","gene_name":"protein phosphatase 2C like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28406]","synonyms":"FLJ25449,C3orf48","biotype":"protein_coding","ncbi_id":"151649","summary":null,"start":19979961,"end":20012330,"strand":-1,"description":"protein phosphatase 2C like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28406]"}, {"versioned_ensembl_gene_id":"ENSG00000211806.2","gene_symbol":"TRAV25","gene_name":"T-cell receptor alpha variable 25 [Source:HGNC Symbol;Acc:HGNC:12122]","synonyms":"TCRAV32S1,TCRAV25S1","biotype":"TR_V_gene","ncbi_id":"28658","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22112347,"end":22113031,"strand":1,"description":"T-cell receptor alpha variable 25 [Source:HGNC Symbol;Acc:HGNC:12122]"}, {"versioned_ensembl_gene_id":"ENSG00000102445.18","gene_symbol":"RUBCNL","gene_name":"RUN and cysteine rich domain containing beclin 1 interacting protein like [Source:HGNC Symbol;Acc:HGNC:20420]","synonyms":"KIAA0226L,FLJ21562,C13orf18","biotype":"protein_coding","ncbi_id":"80183","summary":"This gene encodes a cysteine-rich protein that contains a putative zinc-RING and/or ribbon domain. The encoded protein is related to Run domain Beclin-1-interacting and cysteine-rich domain-containing protein, which plays a role in endocytic trafficking and autophagy. In cervical cancer cell lines, this gene is expressed at low levels and may function as a tumor suppressor. Promoter hypermethylation of this gene is observed in cervical cancer cell lines and tissue derived from human patients. [provided by RefSeq, Mar 2017]","start":46342000,"end":46438190,"strand":-1,"description":"RUN and cysteine rich domain containing beclin 1 interacting protein like [Source:HGNC Symbol;Acc:HGNC:20420]"}, {"versioned_ensembl_gene_id":"ENSG00000211799.3","gene_symbol":"TRAV19","gene_name":"T-cell receptor alpha variable 19 [Source:HGNC Symbol;Acc:HGNC:12115]","synonyms":"TCRAV19S1,TCRAV12S1","biotype":"TR_V_gene","ncbi_id":"28664","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22007512,"end":22008181,"strand":1,"description":"T-cell receptor alpha variable 19 [Source:HGNC Symbol;Acc:HGNC:12115]"}, {"versioned_ensembl_gene_id":"ENSG00000280406.1","gene_symbol":"AC104985.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34221007,"end":34221603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228518.1","gene_symbol":"SURF6P1","gene_name":"surfeit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37722]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643470","summary":null,"start":17192826,"end":17193652,"strand":1,"description":"surfeit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37722]"}, {"versioned_ensembl_gene_id":"ENSG00000284512.1","gene_symbol":"AC092718.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":81022316,"end":81096284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211798.3","gene_symbol":"TRAV18","gene_name":"T-cell receptor alpha variable 18 [Source:HGNC Symbol;Acc:HGNC:12114]","synonyms":"TCRAV18S1","biotype":"TR_V_gene","ncbi_id":"28665","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22003106,"end":22003673,"strand":1,"description":"T-cell receptor alpha variable 18 [Source:HGNC Symbol;Acc:HGNC:12114]"}, {"versioned_ensembl_gene_id":"ENSG00000262471.1","gene_symbol":"AC009171.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4130555,"end":4130820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226376.1","gene_symbol":"AL135923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7930827,"end":7935137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230724.9","gene_symbol":"LINC01001","gene_name":"long intergenic non-protein coding RNA 1001 [Source:HGNC Symbol;Acc:HGNC:38540]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133161","summary":null,"start":127204,"end":139612,"strand":-1,"description":"long intergenic non-protein coding RNA 1001 [Source:HGNC Symbol;Acc:HGNC:38540]"}, {"versioned_ensembl_gene_id":"ENSG00000168906.12","gene_symbol":"MAT2A","gene_name":"methionine adenosyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:6904]","synonyms":"SAMS2,MATII,MATA2","biotype":"protein_coding","ncbi_id":"4144","summary":"The protein encoded by this gene catalyzes the production of S-adenosylmethionine (AdoMet) from methionine and ATP. AdoMet is the key methyl donor in cellular processes. [provided by RefSeq, Jun 2011]","start":85539165,"end":85545280,"strand":1,"description":"methionine adenosyltransferase 2A [Source:HGNC Symbol;Acc:HGNC:6904]"}, {"versioned_ensembl_gene_id":"ENSG00000234636.2","gene_symbol":"MED14OS","gene_name":"MED14 opposite strand [Source:HGNC Symbol;Acc:HGNC:40162]","synonyms":"MED14-AS1","biotype":"protein_coding","ncbi_id":"100873985","summary":null,"start":40735400,"end":40738701,"strand":1,"description":"MED14 opposite strand [Source:HGNC Symbol;Acc:HGNC:40162]"}, {"versioned_ensembl_gene_id":"ENSG00000211795.3","gene_symbol":"TRAV8-6","gene_name":"T-cell receptor alpha variable 8-6 [Source:HGNC Symbol;Acc:HGNC:12151]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28680","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21978459,"end":21979120,"strand":1,"description":"T-cell receptor alpha variable 8-6 [Source:HGNC Symbol;Acc:HGNC:12151]"}, {"versioned_ensembl_gene_id":"ENSG00000276461.4","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"AR1,SPBP","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42160013,"end":42215442,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000134283.17","gene_symbol":"PPHLN1","gene_name":"periphilin 1 [Source:HGNC Symbol;Acc:HGNC:19369]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51535","summary":"The protein encoded by this gene is one of the several proteins that become sequentially incorporated into the cornified cell envelope during the terminal differentiation of keratinocyte at the outer layers of epidermis. This protein interacts with periplakin, which is known as a precursor of the cornified cell envelope. The cellular localization pattern and insolubility of this protein suggest that it may play a role in epithelial differentiation and contribute to epidermal integrity and barrier formation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":42238447,"end":42459715,"strand":1,"description":"periphilin 1 [Source:HGNC Symbol;Acc:HGNC:19369]"}, {"versioned_ensembl_gene_id":"ENSG00000258068.1","gene_symbol":"AC079600.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42485353,"end":42490019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172954.13","gene_symbol":"LCLAT1","gene_name":"lysocardiolipin acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26756]","synonyms":"LYCAT,FLJ37965,ALCAT1,AGPAT8","biotype":"protein_coding","ncbi_id":"253558","summary":null,"start":30447226,"end":30644225,"strand":1,"description":"lysocardiolipin acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26756]"}, {"versioned_ensembl_gene_id":"ENSG00000225737.9","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"HLP,SKIV2,DDX13,SKI2W,170A,SKIV2L1","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31946626,"end":31957297,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000233518.1","gene_symbol":"RPL7P35","gene_name":"ribosomal protein L7 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271216","summary":null,"start":110550115,"end":110550854,"strand":-1,"description":"ribosomal protein L7 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36153]"}, {"versioned_ensembl_gene_id":"ENSG00000267397.1","gene_symbol":"AC090229.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35716370,"end":35717978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229275.1","gene_symbol":"BX284656.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48141542,"end":48143229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261173.1","gene_symbol":"AC018845.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46973989,"end":46978983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231466.2","gene_symbol":"AL022324.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25349543,"end":25350322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232601.1","gene_symbol":"AC069218.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174302944,"end":174303287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154359.12","gene_symbol":"LONRF1","gene_name":"LON peptidase N-terminal domain and ring finger 1 [Source:HGNC Symbol;Acc:HGNC:26302]","synonyms":"RNF191,FLJ23749","biotype":"protein_coding","ncbi_id":"91694","summary":null,"start":12721894,"end":12756073,"strand":-1,"description":"LON peptidase N-terminal domain and ring finger 1 [Source:HGNC Symbol;Acc:HGNC:26302]"}, {"versioned_ensembl_gene_id":"ENSG00000170365.9","gene_symbol":"SMAD1","gene_name":"SMAD family member 1 [Source:HGNC Symbol;Acc:HGNC:6767]","synonyms":"MADR1,MADH1,JV4-1","biotype":"protein_coding","ncbi_id":"4086","summary":"The protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signals of the bone morphogenetic proteins (BMPs), which are involved in a range of biological activities including cell growth, apoptosis, morphogenesis, development and immune responses. In response to BMP ligands, this protein can be phosphorylated and activated by the BMP receptor kinase. The phosphorylated form of this protein forms a complex with SMAD4, which is important for its function in the transcription regulation. This protein is a target for SMAD-specific E3 ubiquitin ligases, such as SMURF1 and SMURF2, and undergoes ubiquitination and proteasome-mediated degradation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":145481194,"end":145558079,"strand":1,"description":"SMAD family member 1 [Source:HGNC Symbol;Acc:HGNC:6767]"}, {"versioned_ensembl_gene_id":"ENSG00000236609.3","gene_symbol":"ZNF853","gene_name":"zinc finger protein 853 [Source:HGNC Symbol;Acc:HGNC:21767]","synonyms":"DKFZp434J1015","biotype":"protein_coding","ncbi_id":"54753","summary":null,"start":6615617,"end":6624290,"strand":1,"description":"zinc finger protein 853 [Source:HGNC Symbol;Acc:HGNC:21767]"}, {"versioned_ensembl_gene_id":"ENSG00000237642.1","gene_symbol":"HMGB3P5","gene_name":"high mobility group box 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39105]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645360","summary":null,"start":110450629,"end":110451240,"strand":1,"description":"high mobility group box 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39105]"}, {"versioned_ensembl_gene_id":"ENSG00000235561.1","gene_symbol":"CR759281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30349532,"end":30350165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273785.2","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42149871,"end":42155001,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000249053.1","gene_symbol":"AC106794.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12794731,"end":12795522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000024526.16","gene_symbol":"DEPDC1","gene_name":"DEP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22949]","synonyms":"SDP35,FLJ20354,DEPDC1A,DEP.8","biotype":"protein_coding","ncbi_id":"55635","summary":null,"start":68474152,"end":68497221,"strand":-1,"description":"DEP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22949]"}, {"versioned_ensembl_gene_id":"ENSG00000268941.2","gene_symbol":"LINC01711","gene_name":"long intergenic non-protein coding RNA 1711 [Source:HGNC Symbol;Acc:HGNC:28663]","synonyms":"MGC4294","biotype":"lincRNA","ncbi_id":"79160","summary":null,"start":58634772,"end":58635738,"strand":1,"description":"long intergenic non-protein coding RNA 1711 [Source:HGNC Symbol;Acc:HGNC:28663]"}, {"versioned_ensembl_gene_id":"ENSG00000248783.1","gene_symbol":"AC106771.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12553890,"end":12574637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226165.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32847708,"end":32855144,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000254468.2","gene_symbol":"AC069287.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112967,"end":125927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277211.1","gene_symbol":"AC092132.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20155648,"end":20158391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237035.1","gene_symbol":"AC020719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198187802,"end":198191521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180269.7","gene_symbol":"GPR139","gene_name":"G protein-coupled receptor 139 [Source:HGNC Symbol;Acc:HGNC:19995]","synonyms":"PGR3","biotype":"protein_coding","ncbi_id":"124274","summary":"This gene encodes a member of the rhodopsin family of G-protein-coupled receptors. The encoded protein is almost exclusively expressed in the central nervous system. L-tryptophan and L-phenylalanine may act as the physiologic ligands of the encoded protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":20031485,"end":20073917,"strand":-1,"description":"G protein-coupled receptor 139 [Source:HGNC Symbol;Acc:HGNC:19995]"}, {"versioned_ensembl_gene_id":"ENSG00000135048.13","gene_symbol":"TMEM2","gene_name":"transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:11869]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23670","summary":"This gene encodes a type II transmembrane protein that belongs to the interferon-induced transmembrane (IFITM) protein superfamily. The encoded protein functions as a cell surface hyaluronidase that cleaves extracellular high molecular weight hyaluronan into intermediate size fragments before internalization and degradation in the lysosome. It also has an interferon-mediated antiviral function in humans through activation of the JAK STAT signaling pathway. The activation of this gene by transcription factor SOX4 in breast cancer cells has been shown to mediate the pathological effects of SOX4 on cancer progression. Naturally occurring mutations in this gene are associated with autosomal recessive non-syndromic hearing loss. [provided by RefSeq, Mar 2017]","start":71683366,"end":71816690,"strand":-1,"description":"transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:11869]"}, {"versioned_ensembl_gene_id":"ENSG00000234065.2","gene_symbol":"MTND4P26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42213]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873247","summary":null,"start":120213631,"end":120214989,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42213]"}, {"versioned_ensembl_gene_id":"ENSG00000254724.1","gene_symbol":"OR7E10P","gene_name":"olfactory receptor family 7 subfamily E member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:8381]","synonyms":"OR11-1","biotype":"unprocessed_pseudogene","ncbi_id":"10823","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":12703066,"end":12704056,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:8381]"}, {"versioned_ensembl_gene_id":"ENSG00000230326.1","gene_symbol":"HMGN1P33","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874446","summary":null,"start":9865093,"end":9865543,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39377]"}, {"versioned_ensembl_gene_id":"ENSG00000171824.13","gene_symbol":"EXOSC10","gene_name":"exosome component 10 [Source:HGNC Symbol;Acc:HGNC:9138]","synonyms":"Rrp6p,RRP6,PMSCL2,PM/Scl-100,PM-Scl,p4,p3,p2","biotype":"protein_coding","ncbi_id":"5394","summary":null,"start":11066618,"end":11099881,"strand":-1,"description":"exosome component 10 [Source:HGNC Symbol;Acc:HGNC:9138]"}, {"versioned_ensembl_gene_id":"ENSG00000243853.1","gene_symbol":"ALDH7A1P3","gene_name":"aldehyde dehydrogenase 7 family member A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:880]","synonyms":"ATQL3","biotype":"processed_pseudogene","ncbi_id":"543","summary":null,"start":150541754,"end":150542098,"strand":-1,"description":"aldehyde dehydrogenase 7 family member A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:880]"}, {"versioned_ensembl_gene_id":"ENSG00000276370.2","gene_symbol":"PRAMEF33","gene_name":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]","synonyms":"PRAMEF33P,PRAMEF33P","biotype":"protein_coding","ncbi_id":"645382","summary":null,"start":13322112,"end":13327566,"strand":1,"description":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]"}, {"versioned_ensembl_gene_id":"ENSG00000254237.5","gene_symbol":"AC021242.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9371970,"end":9436205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103811.15","gene_symbol":"CTSH","gene_name":"cathepsin H [Source:HGNC Symbol;Acc:HGNC:2535]","synonyms":"CPSB,ACC5,ACC4,ACC-5,ACC-4","biotype":"protein_coding","ncbi_id":"1512","summary":"The protein encoded by this gene is a lysosomal cysteine proteinase important in the overall degradation of lysosomal proteins. It is composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor. The encoded protein, which belongs to the peptidase C1 protein family, can act both as an aminopeptidase and as an endopeptidase. Increased expression of this gene has been correlated with malignant progression of prostate tumors. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":78921058,"end":78949574,"strand":-1,"description":"cathepsin H [Source:HGNC Symbol;Acc:HGNC:2535]"}, {"versioned_ensembl_gene_id":"ENSG00000259274.1","gene_symbol":"AC107241.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60529973,"end":60545159,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236641.1","gene_symbol":"Z99916.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25212742,"end":25213685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226626.2","gene_symbol":"NOP56P2","gene_name":"NOP56 ribonucleoprotein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402360","summary":null,"start":23681894,"end":23682662,"strand":1,"description":"NOP56 ribonucleoprotein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49800]"}, {"versioned_ensembl_gene_id":"ENSG00000260078.3","gene_symbol":"AC007342.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53364982,"end":53373083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262185.1","gene_symbol":"AC005736.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3947609,"end":3950444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283674.2","gene_symbol":"AC068587.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":12467693,"end":12665588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284663.1","gene_symbol":"AC068587.8","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12607291,"end":12607509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254023.1","gene_symbol":"PKMP4","gene_name":"pyruvate kinase, muscle pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44246]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480443","summary":null,"start":75376709,"end":75377014,"strand":1,"description":"pyruvate kinase, muscle pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44246]"}, {"versioned_ensembl_gene_id":"ENSG00000255549.2","gene_symbol":"ENPP7P6","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48698]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107133511","summary":null,"start":12448013,"end":12511278,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48698]"}, {"versioned_ensembl_gene_id":"ENSG00000255253.1","gene_symbol":"AC068587.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12638428,"end":12638602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223799.1","gene_symbol":"IL10RB-AS1","gene_name":"IL10RB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44303]","synonyms":"IFNAR2-AS1","biotype":"antisense_RNA","ncbi_id":"100288432","summary":null,"start":33263873,"end":33266260,"strand":-1,"description":"IL10RB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44303]"}, {"versioned_ensembl_gene_id":"ENSG00000260509.2","gene_symbol":"AL590787.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25300124,"end":25301438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281371.1","gene_symbol":"INE2","gene_name":"inactivation escape 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6061]","synonyms":"NCRNA00011","biotype":"antisense_RNA","ncbi_id":"8551","summary":null,"start":15785716,"end":15787589,"strand":-1,"description":"inactivation escape 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6061]"}, {"versioned_ensembl_gene_id":"ENSG00000144659.10","gene_symbol":"SLC25A38","gene_name":"solute carrier family 25 member 38 [Source:HGNC Symbol;Acc:HGNC:26054]","synonyms":"FLJ20551","biotype":"protein_coding","ncbi_id":"54977","summary":"This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]","start":39383348,"end":39397351,"strand":1,"description":"solute carrier family 25 member 38 [Source:HGNC Symbol;Acc:HGNC:26054]"}, {"versioned_ensembl_gene_id":"ENSG00000253346.1","gene_symbol":"AC109329.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30331961,"end":30332277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255621.1","gene_symbol":"AC023790.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13000451,"end":13040679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274109.2","gene_symbol":"HNRNPCL2","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]","synonyms":"HNRNPCP5,HNRNPCP5","biotype":"protein_coding","ncbi_id":"440563","summary":null,"start":13136151,"end":13137509,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]"}, {"versioned_ensembl_gene_id":"ENSG00000273585.1","gene_symbol":"LINC02348","gene_name":"long intergenic non-protein coding RNA 2348 [Source:HGNC Symbol;Acc:HGNC:53270]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927505","summary":null,"start":101613676,"end":101614339,"strand":-1,"description":"long intergenic non-protein coding RNA 2348 [Source:HGNC Symbol;Acc:HGNC:53270]"}, {"versioned_ensembl_gene_id":"ENSG00000282077.1","gene_symbol":"PATL2","gene_name":"PAT1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:33630]","synonyms":"Pat1a","biotype":"processed_transcript","ncbi_id":"197135","summary":null,"start":44711032,"end":44711328,"strand":1,"description":"PAT1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:33630]"}, {"versioned_ensembl_gene_id":"ENSG00000282700.1","gene_symbol":"AC018901.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44679746,"end":44684155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168961.16","gene_symbol":"LGALS9","gene_name":"galectin 9 [Source:HGNC Symbol;Acc:HGNC:6570]","synonyms":"LGALS9A","biotype":"protein_coding","ncbi_id":"3965","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. The protein encoded by this gene is an S-type lectin. It is overexpressed in Hodgkin's disease tissue and might participate in the interaction between the H&RS cells with their surrounding cells and might thus play a role in the pathogenesis of this disease and/or its associated immunodeficiency. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":27629798,"end":27649560,"strand":1,"description":"galectin 9 [Source:HGNC Symbol;Acc:HGNC:6570]"}, {"versioned_ensembl_gene_id":"ENSG00000277853.2","gene_symbol":"PRAMEF18","gene_name":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391003","summary":null,"start":13241912,"end":13244686,"strand":-1,"description":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]"}, {"versioned_ensembl_gene_id":"ENSG00000223549.1","gene_symbol":"MTND5P28","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505755","summary":null,"start":120215181,"end":120217279,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42290]"}, {"versioned_ensembl_gene_id":"ENSG00000281573.1","gene_symbol":"PRAMEF9","gene_name":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343070","summary":null,"start":13191011,"end":13198026,"strand":1,"description":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]"}, {"versioned_ensembl_gene_id":"ENSG00000172752.14","gene_symbol":"COL6A5","gene_name":"collagen type VI alpha 5 chain [Source:HGNC Symbol;Acc:HGNC:26674]","synonyms":"FLJ35880,COL29A1,VWA4","biotype":"protein_coding","ncbi_id":"256076","summary":"This gene encodes a member of the collagen superfamily of proteins. The encoded protein contains multiple von Willebrand factor A-like domains and may interact with the alpha 1 and alpha 2 chains of collagen VI to form the complete collagen VI trimer. Polymorphisms in this gene may be linked to dermal phenotypes, such as eczema. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":130345516,"end":130484844,"strand":1,"description":"collagen type VI alpha 5 chain [Source:HGNC Symbol;Acc:HGNC:26674]"}, {"versioned_ensembl_gene_id":"ENSG00000159842.14","gene_symbol":"ABR","gene_name":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]","synonyms":"MDB","biotype":"protein_coding","ncbi_id":"29","summary":"This gene encodes a protein that is similar to the protein encoded by the breakpoint cluster region gene located on chromosome 22. The protein encoded by this gene contains a GTPase-activating protein domain, a domain found in members of the Rho family of GTP-binding proteins. Functional studies in mice determined that this protein plays a role in vestibular morphogenesis. Alternatively spliced transcript variants have been reported for this gene. [provided by RefSeq, Feb 2012]","start":1003518,"end":1229021,"strand":-1,"description":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]"}, {"versioned_ensembl_gene_id":"ENSG00000269145.2","gene_symbol":"AC007192.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18144522,"end":18151691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166946.13","gene_symbol":"CCNDBP1","gene_name":"cyclin D1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1587]","synonyms":"HHM,GCIP,DIP1","biotype":"protein_coding","ncbi_id":"23582","summary":"This gene was identified by the interaction of its gene product with Grap2, a leukocyte-specific adaptor protein important for immune cell signaling. The protein encoded by this gene was shown to interact with cyclin D. Transfection of this gene in cells was reported to reduce the phosphorylation of Rb gene product by cyclin D-dependent protein kinase, and inhibit E2F1-mediated transcription activity. This protein was also found to interact with helix-loop-helix protein E12 and is thought to be a negative regulator of liver-specific gene expression. Several alternatively spliced variants have been found for this gene. [provided by RefSeq, Apr 2009]","start":43185118,"end":43197176,"strand":1,"description":"cyclin D1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1587]"}, {"versioned_ensembl_gene_id":"ENSG00000244652.1","gene_symbol":"AC079382.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106325737,"end":106326293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183199.6","gene_symbol":"AC093768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87891843,"end":87894015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231401.1","gene_symbol":"AC023481.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8364707,"end":8366392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215302.8","gene_symbol":"AC127502.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30470779,"end":30507623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137103.17","gene_symbol":"TMEM8B","gene_name":"transmembrane protein 8B [Source:HGNC Symbol;Acc:HGNC:21427]","synonyms":"NGX6,NAG-5,C9orf127","biotype":"protein_coding","ncbi_id":"51754","summary":null,"start":35814451,"end":35865518,"strand":1,"description":"transmembrane protein 8B [Source:HGNC Symbol;Acc:HGNC:21427]"}, {"versioned_ensembl_gene_id":"ENSG00000283345.1","gene_symbol":"AC127502.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30507377,"end":30513698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228686.2","gene_symbol":"AL590723.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176017277,"end":176018760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224398.7","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb1,Ckb2","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31741515,"end":31749825,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000232751.1","gene_symbol":"AL645568.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173351689,"end":173352004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260594.1","gene_symbol":"AC099313.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80736360,"end":80742305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269099.2","gene_symbol":"LSP1P1","gene_name":"lymphocyte-specific protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100463528","summary":null,"start":25017404,"end":25017536,"strand":1,"description":"lymphocyte-specific protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39716]"}, {"versioned_ensembl_gene_id":"ENSG00000184809.12","gene_symbol":"B3GALT5-AS1","gene_name":"B3GALT5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16424]","synonyms":"C21orf88","biotype":"antisense_RNA","ncbi_id":"114041","summary":null,"start":39597147,"end":39612821,"strand":-1,"description":"B3GALT5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16424]"}, {"versioned_ensembl_gene_id":"ENSG00000224121.1","gene_symbol":"ATG12P2","gene_name":"autophagy related 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38605]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100293948","summary":null,"start":222904640,"end":222905055,"strand":-1,"description":"autophagy related 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38605]"}, {"versioned_ensembl_gene_id":"ENSG00000227110.6","gene_symbol":"LMCD1-AS1","gene_name":"LMCD1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44477]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288428","summary":null,"start":7952805,"end":8611924,"strand":-1,"description":"LMCD1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44477]"}, {"versioned_ensembl_gene_id":"ENSG00000271937.1","gene_symbol":"AC104187.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44337941,"end":44338552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262025.1","gene_symbol":"AL513523.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153869337,"end":153870645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241859.6","gene_symbol":"ANOS2P","gene_name":"anosmin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:6214]","synonyms":"KALP,KAL-Y,ADMLY","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3734","summary":null,"start":13751656,"end":13915824,"strand":1,"description":"anosmin 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:6214]"}, {"versioned_ensembl_gene_id":"ENSG00000244235.2","gene_symbol":"AC103724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42101318,"end":42101836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131142.13","gene_symbol":"CCL25","gene_name":"C-C motif chemokine ligand 25 [Source:HGNC Symbol;Acc:HGNC:10624]","synonyms":"TECK,SCYA25,Ckb15","biotype":"protein_coding","ncbi_id":"6370","summary":"This antimicrobial gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for dendritic cells, thymocytes, and activated macrophages but is inactive on peripheral blood lymphocytes and neutrophils. The product of this gene binds to chemokine receptor CCR9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":8052767,"end":8062650,"strand":1,"description":"C-C motif chemokine ligand 25 [Source:HGNC Symbol;Acc:HGNC:10624]"}, {"versioned_ensembl_gene_id":"ENSG00000203616.2","gene_symbol":"RHOT1P2","gene_name":"ras homolog family member T1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37838]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462811","summary":null,"start":13936993,"end":13937325,"strand":-1,"description":"ras homolog family member T1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37838]"}, {"versioned_ensembl_gene_id":"ENSG00000115317.11","gene_symbol":"HTRA2","gene_name":"HtrA serine peptidase 2 [Source:HGNC Symbol;Acc:HGNC:14348]","synonyms":"PRSS25,PARK13,OMI","biotype":"protein_coding","ncbi_id":"27429","summary":"This gene encodes a serine protease. The protein has been localized in the endoplasmic reticulum and interacts with an alternatively spliced form of mitogen-activated protein kinase 14. The protein has also been localized to the mitochondria with release to the cytosol following apoptotic stimulus. The protein is thought to induce apoptosis by binding the apoptosis inhibitory protein baculoviral IAP repeat-containing 4. Nuclear localization of this protein has also been observed. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":74529377,"end":74533348,"strand":1,"description":"HtrA serine peptidase 2 [Source:HGNC Symbol;Acc:HGNC:14348]"}, {"versioned_ensembl_gene_id":"ENSG00000134245.17","gene_symbol":"WNT2B","gene_name":"Wnt family member 2B [Source:HGNC Symbol;Acc:HGNC:12781]","synonyms":"XWNT2,WNT13","biotype":"protein_coding","ncbi_id":"7482","summary":"This gene encodes a member of the wingless-type MMTV integration site (WNT) family of highly conserved, secreted signaling factors. WNT family members function in a variety of developmental processes including regulation of cell growth and differentiation and are characterized by a WNT-core domain. This gene may play a role in human development as well as carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":112466541,"end":112530165,"strand":1,"description":"Wnt family member 2B [Source:HGNC Symbol;Acc:HGNC:12781]"}, {"versioned_ensembl_gene_id":"ENSG00000283849.1","gene_symbol":"AC092053.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39152906,"end":39154723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267140.1","gene_symbol":"AC007998.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35443871,"end":35497940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068745.14","gene_symbol":"IP6K2","gene_name":"inositol hexakisphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:17313]","synonyms":"IHPK2","biotype":"protein_coding","ncbi_id":"51447","summary":"This gene encodes a protein that belongs to the inositol phosphokinase (IPK) family. This protein is likely responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4 and affect the growth suppressive and apoptotic activities of interferon-beta in some ovarian cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":48688003,"end":48740353,"strand":-1,"description":"inositol hexakisphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:17313]"}, {"versioned_ensembl_gene_id":"ENSG00000263878.1","gene_symbol":"DLGAP1-AS4","gene_name":"DLGAP1 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:44333]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410534","summary":null,"start":3962353,"end":4013943,"strand":1,"description":"DLGAP1 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:44333]"}, {"versioned_ensembl_gene_id":"ENSG00000243694.2","gene_symbol":"LINC02027","gene_name":"long intergenic non-protein coding RNA 2027 [Source:HGNC Symbol;Acc:HGNC:52862]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728290","summary":null,"start":80993868,"end":81095647,"strand":1,"description":"long intergenic non-protein coding RNA 2027 [Source:HGNC Symbol;Acc:HGNC:52862]"}, {"versioned_ensembl_gene_id":"ENSG00000154856.12","gene_symbol":"APCDD1","gene_name":"APC down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:15718]","synonyms":"B7323","biotype":"protein_coding","ncbi_id":"147495","summary":"This locus encodes an inhibitor of the Wnt signaling pathway. Mutations at this locus have been associated with hereditary hypotrichosis simplex. Increased expression of this gene may also be associated with colorectal carcinogenesis.[provided by RefSeq, Sep 2010]","start":10454628,"end":10489948,"strand":1,"description":"APC down-regulated 1 [Source:HGNC Symbol;Acc:HGNC:15718]"}, {"versioned_ensembl_gene_id":"ENSG00000134215.15","gene_symbol":"VAV3","gene_name":"vav guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:12659]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10451","summary":"This gene is a member of the VAV gene family. The VAV proteins are guanine nucleotide exchange factors (GEFs) for Rho family GTPases that activate pathways leading to actin cytoskeletal rearrangements and transcriptional alterations. This gene product acts as a GEF preferentially for RhoG, RhoA, and to a lesser extent, RAC1, and it associates maximally with the nucleotide-free states of these GTPases. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":107571160,"end":107965144,"strand":-1,"description":"vav guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:12659]"}, {"versioned_ensembl_gene_id":"ENSG00000236460.1","gene_symbol":"SNX2P2","gene_name":"sorting nexin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873785","summary":null,"start":31941261,"end":31941583,"strand":1,"description":"sorting nexin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41515]"}, {"versioned_ensembl_gene_id":"ENSG00000165730.14","gene_symbol":"STOX1","gene_name":"storkhead box 1 [Source:HGNC Symbol;Acc:HGNC:23508]","synonyms":"FLJ25162,C10orf24","biotype":"protein_coding","ncbi_id":"219736","summary":"The protein encoded by this gene may function as a DNA binding protein. Mutations in this gene are associated with pre-eclampsia/eclampsia 4 (PEE4). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":68827541,"end":68895432,"strand":1,"description":"storkhead box 1 [Source:HGNC Symbol;Acc:HGNC:23508]"}, {"versioned_ensembl_gene_id":"ENSG00000234367.1","gene_symbol":"PFN1P3","gene_name":"profilin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42987]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"200025","summary":null,"start":145407772,"end":145408173,"strand":1,"description":"profilin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42987]"}, {"versioned_ensembl_gene_id":"ENSG00000232927.1","gene_symbol":"USP12PY","gene_name":"ubiquitin specific peptidase 12 pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:23195]","synonyms":"USP12P3","biotype":"processed_pseudogene","ncbi_id":"359799","summary":null,"start":3682805,"end":3683868,"strand":1,"description":"ubiquitin specific peptidase 12 pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:23195]"}, {"versioned_ensembl_gene_id":"ENSG00000116649.9","gene_symbol":"SRM","gene_name":"spermidine synthase [Source:HGNC Symbol;Acc:HGNC:11296]","synonyms":"SRML1,SPS1","biotype":"protein_coding","ncbi_id":"6723","summary":"The polyamines putrescine, spermine, and spermidine are ubiquitous polycationic mediators of cell growth and differentiation. Spermidine synthase is one of four enzymes in the polyamine-biosynthetic pathway and carries out the final step of spermidine biosynthesis. This enzyme catalyzes the conversion of putrescine to spermidine using decarboxylated S-adenosylmethionine as the cofactor. [provided by RefSeq, Jul 2008]","start":11054584,"end":11060024,"strand":-1,"description":"spermidine synthase [Source:HGNC Symbol;Acc:HGNC:11296]"}, {"versioned_ensembl_gene_id":"ENSG00000224142.1","gene_symbol":"AMMECR1-IT1","gene_name":"AMMECR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41306]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874352","summary":null,"start":110305420,"end":110307221,"strand":-1,"description":"AMMECR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41306]"}, {"versioned_ensembl_gene_id":"ENSG00000159840.15","gene_symbol":"ZYX","gene_name":"zyxin [Source:HGNC Symbol;Acc:HGNC:13200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7791","summary":"Focal adhesions are actin-rich structures that enable cells to adhere to the extracellular matrix and at which protein complexes involved in signal transduction assemble. Zyxin is a zinc-binding phosphoprotein that concentrates at focal adhesions and along the actin cytoskeleton. Zyxin has an N-terminal proline-rich domain and three LIM domains in its C-terminal half. The proline-rich domain may interact with SH3 domains of proteins involved in signal transduction pathways while the LIM domains are likely involved in protein-protein binding. Zyxin may function as a messenger in the signal transduction pathway that mediates adhesion-stimulated changes in gene expression and may modulate the cytoskeletal organization of actin bundles. Alternative splicing results in multiple transcript variants that encode the same isoform. [provided by RefSeq, Jul 2008]","start":143381080,"end":143391111,"strand":1,"description":"zyxin [Source:HGNC Symbol;Acc:HGNC:13200]"}, {"versioned_ensembl_gene_id":"ENSG00000250363.1","gene_symbol":"KRT18P21","gene_name":"keratin 18 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:33389]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"132391","summary":null,"start":115920707,"end":115921978,"strand":1,"description":"keratin 18 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:33389]"}, {"versioned_ensembl_gene_id":"ENSG00000227661.1","gene_symbol":"MTCO3P18","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52048]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075215","summary":null,"start":131380153,"end":131380913,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52048]"}, {"versioned_ensembl_gene_id":"ENSG00000277800.3","gene_symbol":"TBX22","gene_name":"T-box 22 [Source:HGNC Symbol;Acc:HGNC:11600]","synonyms":"CPX,CLPA","biotype":"protein_coding","ncbi_id":"50945","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":80027033,"end":80044046,"strand":1,"description":"T-box 22 [Source:HGNC Symbol;Acc:HGNC:11600]"}, {"versioned_ensembl_gene_id":"ENSG00000248029.2","gene_symbol":"AC034238.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55063179,"end":55066230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270170.1","gene_symbol":"NCBP2-AS2","gene_name":"NCBP2 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:25121]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152217","summary":null,"start":196942623,"end":196943540,"strand":1,"description":"NCBP2 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:25121]"}, {"versioned_ensembl_gene_id":"ENSG00000243811.8","gene_symbol":"APOBEC3D","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3D [Source:HGNC Symbol;Acc:HGNC:17354]","synonyms":"ARP6,APOBEC3E,APOBEC3DE","biotype":"protein_coding","ncbi_id":"140564","summary":"This gene is a member of the cytidine deaminase gene family. It is one of a group of related genes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1 and inhibit retroviruses, such as HIV, by deaminating cytosine residues in nascent retroviral cDNA. [provided by RefSeq, Jul 2008]","start":39021113,"end":39033276,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3D [Source:HGNC Symbol;Acc:HGNC:17354]"}, {"versioned_ensembl_gene_id":"ENSG00000184307.14","gene_symbol":"ZDHHC23","gene_name":"zinc finger DHHC-type containing 23 [Source:HGNC Symbol;Acc:HGNC:28654]","synonyms":"MGC42530","biotype":"protein_coding","ncbi_id":"254887","summary":null,"start":113947901,"end":113965401,"strand":1,"description":"zinc finger DHHC-type containing 23 [Source:HGNC Symbol;Acc:HGNC:28654]"}, {"versioned_ensembl_gene_id":"ENSG00000234913.1","gene_symbol":"AC016027.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18004270,"end":18007308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140853.15","gene_symbol":"NLRC5","gene_name":"NLR family CARD domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29933]","synonyms":"NOD27,FLJ21709,CLR16.1","biotype":"protein_coding","ncbi_id":"84166","summary":"This gene encodes a member of the caspase recruitment domain-containing NLR family. This gene plays a role in cytokine response and antiviral immunity through its inhibition of NF-kappa-B activation and negative regulation of type I interferon signaling pathways. [provided by RefSeq, Oct 2011]","start":56989485,"end":57083531,"strand":1,"description":"NLR family CARD domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29933]"}, {"versioned_ensembl_gene_id":"ENSG00000234624.2","gene_symbol":"AC016894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61416887,"end":61417197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007001.12","gene_symbol":"UPP2","gene_name":"uridine phosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:23061]","synonyms":"UPASE2,UP2,UDRPASE2","biotype":"protein_coding","ncbi_id":"151531","summary":null,"start":157876702,"end":158136154,"strand":1,"description":"uridine phosphorylase 2 [Source:HGNC Symbol;Acc:HGNC:23061]"}, {"versioned_ensembl_gene_id":"ENSG00000181741.7","gene_symbol":"FDX1P1","gene_name":"ferredoxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3640]","synonyms":"FDXP1,ADXP1","biotype":"processed_pseudogene","ncbi_id":"2231","summary":null,"start":34475924,"end":34476474,"strand":-1,"description":"ferredoxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3640]"}, {"versioned_ensembl_gene_id":"ENSG00000164093.15","gene_symbol":"PITX2","gene_name":"paired like homeodomain 2 [Source:HGNC Symbol;Acc:HGNC:9005]","synonyms":"RIEG,RGS,Otlx2,IRID2,IHG2,IGDS,Brx1,ARP1,RS,RIEG1","biotype":"protein_coding","ncbi_id":"5308","summary":"This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":110617423,"end":110642123,"strand":-1,"description":"paired like homeodomain 2 [Source:HGNC Symbol;Acc:HGNC:9005]"}, {"versioned_ensembl_gene_id":"ENSG00000235366.2","gene_symbol":"LINC01055","gene_name":"long intergenic non-protein coding RNA 1055 [Source:HGNC Symbol;Acc:HGNC:49049]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103752581","summary":null,"start":45680184,"end":45701184,"strand":-1,"description":"long intergenic non-protein coding RNA 1055 [Source:HGNC Symbol;Acc:HGNC:49049]"}, {"versioned_ensembl_gene_id":"ENSG00000279250.1","gene_symbol":"AC022919.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48755693,"end":48756318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218632.3","gene_symbol":"RPL7P28","gene_name":"ribosomal protein L7 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35899]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442242","summary":null,"start":109327175,"end":109327914,"strand":-1,"description":"ribosomal protein L7 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35899]"}, {"versioned_ensembl_gene_id":"ENSG00000204183.1","gene_symbol":"GDF5OS","gene_name":"growth differentiation factor 5 opposite strand [Source:HGNC Symbol;Acc:HGNC:33435]","synonyms":null,"biotype":"protein_coding","ncbi_id":"554250","summary":null,"start":35433029,"end":35435450,"strand":1,"description":"growth differentiation factor 5 opposite strand [Source:HGNC Symbol;Acc:HGNC:33435]"}, {"versioned_ensembl_gene_id":"ENSG00000233285.1","gene_symbol":"MTCYBP10","gene_name":"mitochondrially encoded cytochrome b pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51961]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075121","summary":null,"start":131369062,"end":131369711,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51961]"}, {"versioned_ensembl_gene_id":"ENSG00000249016.1","gene_symbol":"AC112198.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54956235,"end":54957846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162944.10","gene_symbol":"RFTN2","gene_name":"raftlin family member 2 [Source:HGNC Symbol;Acc:HGNC:26402]","synonyms":"FLJ30574,C2orf11,Raftlin-2","biotype":"protein_coding","ncbi_id":"130132","summary":null,"start":197568224,"end":197676045,"strand":-1,"description":"raftlin family member 2 [Source:HGNC Symbol;Acc:HGNC:26402]"}, {"versioned_ensembl_gene_id":"ENSG00000271269.1","gene_symbol":"AL353778.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182733792,"end":182734779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249843.1","gene_symbol":"AC112198.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54878238,"end":54878588,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275723.4","gene_symbol":"NAPEPLD","gene_name":"N-acyl phosphatidylethanolamine phospholipase D [Source:HGNC Symbol;Acc:HGNC:21683]","synonyms":"NAPE-PLD,FMP30,C7orf18","biotype":"protein_coding","ncbi_id":"222236","summary":"NAPEPLD is a phospholipase D type enzyme that catalyzes the release of N-acylethanolamine (NAE) from N-acyl-phosphatidylethanolamine (NAPE) in the second step of the biosynthesis of N-acylethanolamine (Okamoto et al., 2004 [PubMed 14634025]).[supplied by OMIM, Oct 2008]","start":103099776,"end":103149564,"strand":-1,"description":"N-acyl phosphatidylethanolamine phospholipase D [Source:HGNC Symbol;Acc:HGNC:21683]"}, {"versioned_ensembl_gene_id":"ENSG00000053747.15","gene_symbol":"LAMA3","gene_name":"laminin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6483]","synonyms":"nicein-150kDa,LAMNA,kalinin-165kDa,epiligrin,BM600-150kDa","biotype":"protein_coding","ncbi_id":"3909","summary":"The protein encoded by this gene belongs to the laminin family of secreted molecules. Laminins are heterotrimeric molecules that consist of alpha, beta, and gamma subunits that assemble through a coiled-coil domain. Laminins are essential for formation and function of the basement membrane and have additional functions in regulating cell migration and mechanical signal transduction. This gene encodes an alpha subunit and is responsive to several epithelial-mesenchymal regulators including keratinocyte growth factor, epidermal growth factor and insulin-like growth factor. Mutations in this gene have been identified as the cause of Herlitz type junctional epidermolysis bullosa and laryngoonychocutaneous syndrome. Alternative splicing and alternative promoter usage result in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":23689443,"end":23955066,"strand":1,"description":"laminin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6483]"}, {"versioned_ensembl_gene_id":"ENSG00000080493.15","gene_symbol":"SLC4A4","gene_name":"solute carrier family 4 member 4 [Source:HGNC Symbol;Acc:HGNC:11030]","synonyms":"SLC4A5,pNBC,NBC2,NBC1,HNBC1,hhNMC","biotype":"protein_coding","ncbi_id":"8671","summary":"This gene encodes a sodium bicarbonate cotransporter (NBC) involved in the regulation of bicarbonate secretion and absorption and intracellular pH. Mutations in this gene are associated with proximal renal tubular acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":71186757,"end":71572087,"strand":1,"description":"solute carrier family 4 member 4 [Source:HGNC Symbol;Acc:HGNC:11030]"}, {"versioned_ensembl_gene_id":"ENSG00000276480.5","gene_symbol":"MYH11","gene_name":"myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]","synonyms":"SMMHC,SMHC","biotype":"protein_coding","ncbi_id":"4629","summary":"The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alternative splicing generates isoforms that are differentially expressed, with ratios changing during muscle cell maturation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":15788326,"end":15942169,"strand":-1,"description":"myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]"}, {"versioned_ensembl_gene_id":"ENSG00000101191.16","gene_symbol":"DIDO1","gene_name":"death inducer-obliterator 1 [Source:HGNC Symbol;Acc:HGNC:2680]","synonyms":"KIAA0333,FLJ11265,dJ885L7.8,DIO1,DIO-1,DATF1,C20orf158,BYE1","biotype":"protein_coding","ncbi_id":"11083","summary":"Apoptosis, a major form of cell death, is an efficient mechanism for eliminating unwanted cells and is of central importance for development and homeostasis in metazoan animals. In mice, the death inducer-obliterator-1 gene is upregulated by apoptotic signals and encodes a cytoplasmic protein that translocates to the nucleus upon apoptotic signal activation. When overexpressed, the mouse protein induced apoptosis in cell lines growing in vitro. This gene is similar to the mouse gene and therefore is thought to be involved in apoptosis. Alternatively spliced transcripts have been found for this gene, encoding multiple isoforms. [provided by RefSeq, Jul 2008]","start":62877738,"end":62937952,"strand":-1,"description":"death inducer-obliterator 1 [Source:HGNC Symbol;Acc:HGNC:2680]"}, {"versioned_ensembl_gene_id":"ENSG00000170017.12","gene_symbol":"ALCAM","gene_name":"activated leukocyte cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:400]","synonyms":"MEMD,CD166","biotype":"protein_coding","ncbi_id":"214","summary":"This gene encodes activated leukocyte cell adhesion molecule (ALCAM), also known as CD166 (cluster of differentiation 166), which is a member of a subfamily of immunoglobulin receptors with five immunoglobulin-like domains (VVC2C2C2) in the extracellular domain. This protein binds to T-cell differentiation antigene CD6, and is implicated in the processes of cell adhesion and migration. Multiple alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Aug 2011]","start":105366909,"end":105576900,"strand":1,"description":"activated leukocyte cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:400]"}, {"versioned_ensembl_gene_id":"ENSG00000224972.1","gene_symbol":"AL513412.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6902670,"end":6978859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107789.15","gene_symbol":"MINPP1","gene_name":"multiple inositol-polyphosphate phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:7102]","synonyms":"MIPP","biotype":"protein_coding","ncbi_id":"9562","summary":"This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009]","start":87504875,"end":87553460,"strand":1,"description":"multiple inositol-polyphosphate phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:7102]"}, {"versioned_ensembl_gene_id":"ENSG00000162595.5","gene_symbol":"DIRAS3","gene_name":"DIRAS family GTPase 3 [Source:HGNC Symbol;Acc:HGNC:687]","synonyms":"NOEY2,ARHI","biotype":"protein_coding","ncbi_id":"9077","summary":"This gene encodes a member of the ras superfamily. This gene is imprinted gene with monoallelic expression of the paternal allele which is associated with growth suppression. The encoded protein acts as a tumor suppressor whose function is abrogated in many ovarian and breast cancers. This protein may also play a role autophagy in certain cancer cells by regulating the autophagosome initiation complex. [provided by RefSeq, Nov 2015]","start":68045962,"end":68051631,"strand":-1,"description":"DIRAS family GTPase 3 [Source:HGNC Symbol;Acc:HGNC:687]"}, {"versioned_ensembl_gene_id":"ENSG00000225595.2","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401242","summary":null,"start":28859625,"end":28864630,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000278719.1","gene_symbol":"MCM8-AS1","gene_name":"MCM8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51230]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929225","summary":null,"start":5990943,"end":6005821,"strand":-1,"description":"MCM8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51230]"}, {"versioned_ensembl_gene_id":"ENSG00000215869.4","gene_symbol":"AC092506.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":104072983,"end":104226678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267424.1","gene_symbol":"AC020934.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12825711,"end":12832983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152137.6","gene_symbol":"HSPB8","gene_name":"heat shock protein family B (small) member 8 [Source:HGNC Symbol;Acc:HGNC:30171]","synonyms":"HSP22,H11,E2IG1,CMT2L,HspB8","biotype":"protein_coding","ncbi_id":"26353","summary":"The protein encoded by this gene belongs to the superfamily of small heat-shock proteins containing a conservative alpha-crystallin domain at the C-terminal part of the molecule. The expression of this gene in induced by estrogen in estrogen receptor-positive breast cancer cells, and this protein also functions as a chaperone in association with Bag3, a stimulator of macroautophagy. Thus, this gene appears to be involved in regulation of cell proliferation, apoptosis, and carcinogenesis, and mutations in this gene have been associated with different neuromuscular diseases, including Charcot-Marie-Tooth disease. [provided by RefSeq, Jul 2008]","start":119178642,"end":119221131,"strand":1,"description":"heat shock protein family B (small) member 8 [Source:HGNC Symbol;Acc:HGNC:30171]"}, {"versioned_ensembl_gene_id":"ENSG00000284717.1","gene_symbol":"AC087269.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":8714055,"end":8719536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213916.2","gene_symbol":"AL662890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861416,"end":28862047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270321.1","gene_symbol":"AC007953.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177954066,"end":177959798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279690.1","gene_symbol":"AP000280.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32790673,"end":32791504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229303.1","gene_symbol":"PPIAP25","gene_name":"peptidylprolyl isomerase A pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39270]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647085","summary":null,"start":45436121,"end":45436660,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39270]"}, {"versioned_ensembl_gene_id":"ENSG00000169717.6","gene_symbol":"ACTRT2","gene_name":"actin related protein T2 [Source:HGNC Symbol;Acc:HGNC:24026]","synonyms":"FLJ25424,ARPM2,Arp-T2","biotype":"protein_coding","ncbi_id":"140625","summary":"The protein encoded by this intronless gene belongs to the actin family. Studies have shown that this protein may be involved in cytoskeletal organization similar to other cytoplasmic actin-related protein (ARP) subfamily members. Antibody raised against the human protein has been used to detect the protein by immunoblotting and immunofluorescence microscopy, demonstrating its specific synthesis in the testis, late in spermatid differentiation, and its localization in the calyx. [provided by RefSeq, Jul 2008]","start":3021483,"end":3022903,"strand":1,"description":"actin related protein T2 [Source:HGNC Symbol;Acc:HGNC:24026]"}, {"versioned_ensembl_gene_id":"ENSG00000227267.3","gene_symbol":"AC072039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136055184,"end":136055764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231630.1","gene_symbol":"AL592464.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2814432,"end":2814998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270411.1","gene_symbol":"AL354984.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58097267,"end":58097591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214694.10","gene_symbol":"ARHGEF33","gene_name":"Rho guanine nucleotide exchange factor 33 [Source:HGNC Symbol;Acc:HGNC:37252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100271715","summary":null,"start":38889880,"end":38975449,"strand":1,"description":"Rho guanine nucleotide exchange factor 33 [Source:HGNC Symbol;Acc:HGNC:37252]"}, {"versioned_ensembl_gene_id":"ENSG00000253393.1","gene_symbol":"RANP9","gene_name":"RAN, member RAS oncogene family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874193","summary":null,"start":33039523,"end":33039793,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39864]"}, {"versioned_ensembl_gene_id":"ENSG00000243819.4","gene_symbol":"RN7SL832P","gene_name":"RNA, 7SL, cytoplasmic 832, pseudogene [Source:HGNC Symbol;Acc:HGNC:46848]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106479524","summary":null,"start":10690344,"end":10692099,"strand":1,"description":"RNA, 7SL, cytoplasmic 832, pseudogene [Source:HGNC Symbol;Acc:HGNC:46848]"}, {"versioned_ensembl_gene_id":"ENSG00000223731.2","gene_symbol":"SUPT20HL1","gene_name":"SUPT20H like 1 [Source:HGNC Symbol;Acc:HGNC:30773]","synonyms":"SPT20L,FAM48B1","biotype":"processed_pseudogene","ncbi_id":"100130302","summary":null,"start":24362761,"end":24365378,"strand":1,"description":"SUPT20H like 1 [Source:HGNC Symbol;Acc:HGNC:30773]"}, {"versioned_ensembl_gene_id":"ENSG00000224586.6","gene_symbol":"GPX5","gene_name":"glutathione peroxidase 5 [Source:HGNC Symbol;Acc:HGNC:4557]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2880","summary":"This gene belongs to the glutathione peroxidase family. It is specifically expressed in the epididymis in the mammalian male reproductive tract, and is androgen-regulated. Unlike several other characterized glutathione peroxidases, this enzyme is not a selenoprotein, lacking the selenocysteine residue. Thus, it is selenium-independent, and has been proposed to play a role in protecting the membranes of spermatozoa from the damaging effects of lipid peroxidation and/or preventing premature acrosome reaction. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2016]","start":28525925,"end":28534952,"strand":1,"description":"glutathione peroxidase 5 [Source:HGNC Symbol;Acc:HGNC:4557]"}, {"versioned_ensembl_gene_id":"ENSG00000170961.6","gene_symbol":"HAS2","gene_name":"hyaluronan synthase 2 [Source:HGNC Symbol;Acc:HGNC:4819]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3037","summary":" Hyaluronan or hyaluronic acid (HA) is a high molecular weight unbranched polysaccharide synthesized by a wide variety of organisms from bacteria to mammals, and is a constituent of the extracellular matrix. It consists of alternating glucuronic acid and N-acetylglucosamine residues that are linked by beta-1-3 and beta-1-4 glycosidic bonds. HA is synthesized by membrane-bound synthase at the inner surface of the plasma membrane, and the chains are extruded through pore-like structures into the extracellular space. It serves a variety of functions, including space filling, lubrication of joints, and provision of a matrix through which cells can migrate. HA is actively produced during wound healing and tissue repair to provide a framework for ingrowth of blood vessels and fibroblasts. Changes in the serum concentration of HA are associated with inflammatory and degenerative arthropathies such as rheumatoid arthritis. In addition, the interaction of HA with the leukocyte receptor CD44 is important in tissue-specific homing by leukocytes, and overexpression of HA receptors has been correlated with tumor metastasis. HAS2 is a member of the newly identified vertebrate gene family encoding putative hyaluronan synthases, and its amino acid sequence shows significant homology to glycosaminoglycan synthetase (DG42) from Xenopus laevis, and human and murine hyaluronan synthase 1. [provided by RefSeq, Jul 2008]","start":121612116,"end":121641390,"strand":-1,"description":"hyaluronan synthase 2 [Source:HGNC Symbol;Acc:HGNC:4819]"}, {"versioned_ensembl_gene_id":"ENSG00000064601.16","gene_symbol":"CTSA","gene_name":"cathepsin A [Source:HGNC Symbol;Acc:HGNC:9251]","synonyms":"PPGB,GSL","biotype":"protein_coding","ncbi_id":"5476","summary":"This gene encodes a member of the peptidase S10 family of serine carboxypeptidases. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate two chains that comprise the heterodimeric active enzyme. This enzyme possesses deamidase, esterase and carboxypeptidase activities and acts as a scaffold in the lysosomal multienzyme complex. Mutations in this gene are associated with galactosialidosis. [provided by RefSeq, Nov 2015]","start":45890144,"end":45898820,"strand":1,"description":"cathepsin A [Source:HGNC Symbol;Acc:HGNC:9251]"}, {"versioned_ensembl_gene_id":"ENSG00000271984.1","gene_symbol":"AL008726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45892694,"end":45893419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226690.8","gene_symbol":"AC013470.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12469621,"end":12542222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246273.6","gene_symbol":"SBF2-AS1","gene_name":"SBF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27438]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283104","summary":null,"start":9758292,"end":9811319,"strand":1,"description":"SBF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27438]"}, {"versioned_ensembl_gene_id":"ENSG00000237774.3","gene_symbol":"AC126615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95125760,"end":95126389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277517.1","gene_symbol":"AC212493.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":70153120,"end":70181968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214641.3","gene_symbol":"AL445529.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51537155,"end":51537543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130684.13","gene_symbol":"ZNF337","gene_name":"zinc finger protein 337 [Source:HGNC Symbol;Acc:HGNC:15809]","synonyms":"dJ694B14.1","biotype":"protein_coding","ncbi_id":"26152","summary":"This gene encodes a zinc finger domain containing protein. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":25674215,"end":25696841,"strand":-1,"description":"zinc finger protein 337 [Source:HGNC Symbol;Acc:HGNC:15809]"}, {"versioned_ensembl_gene_id":"ENSG00000278383.1","gene_symbol":"AL031673.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25680781,"end":25681246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148426.12","gene_symbol":"PROSER2","gene_name":"proline and serine rich 2 [Source:HGNC Symbol;Acc:HGNC:23728]","synonyms":"MGC35403,C10orf47","biotype":"protein_coding","ncbi_id":"254427","summary":null,"start":11823339,"end":11872277,"strand":1,"description":"proline and serine rich 2 [Source:HGNC Symbol;Acc:HGNC:23728]"}, {"versioned_ensembl_gene_id":"ENSG00000232004.1","gene_symbol":"CAP1P2","gene_name":"CAP1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399748","summary":null,"start":43604843,"end":43606251,"strand":-1,"description":"CAP1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31970]"}, {"versioned_ensembl_gene_id":"ENSG00000213160.9","gene_symbol":"KLHL23","gene_name":"kelch like family member 23 [Source:HGNC Symbol;Acc:HGNC:27506]","synonyms":"MGC2610,MGC22679,FLJ37812","biotype":"protein_coding","ncbi_id":"151230","summary":null,"start":169694488,"end":169776989,"strand":1,"description":"kelch like family member 23 [Source:HGNC Symbol;Acc:HGNC:27506]"}, {"versioned_ensembl_gene_id":"ENSG00000141084.10","gene_symbol":"RANBP10","gene_name":"RAN binding protein 10 [Source:HGNC Symbol;Acc:HGNC:29285]","synonyms":"KIAA1464","biotype":"protein_coding","ncbi_id":"57610","summary":"RAN is a small GTPase involved in the assembly of microtubules to form mitotic spindles. The protein encoded by this gene is a cytoplasmic guanine nucleotide exchange factor (GEF) that binds beta-tubulin and has GEF activity toward RAN. The encoded protein plays a role in the formation of noncentrosomal microtubules. In addition, this protein may be involved in the regulation of D(1) receptor signaling by protein kinase C delta and protein kinase C gamma. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":67723066,"end":67806652,"strand":-1,"description":"RAN binding protein 10 [Source:HGNC Symbol;Acc:HGNC:29285]"}, {"versioned_ensembl_gene_id":"ENSG00000128250.5","gene_symbol":"RFPL1","gene_name":"ret finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:9977]","synonyms":"RNF78","biotype":"protein_coding","ncbi_id":"5988","summary":null,"start":29438583,"end":29442455,"strand":1,"description":"ret finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:9977]"}, {"versioned_ensembl_gene_id":"ENSG00000172164.13","gene_symbol":"SNTB1","gene_name":"syntrophin beta 1 [Source:HGNC Symbol;Acc:HGNC:11168]","synonyms":"TIP-43,SNT2B1,SNT2,BSYN2,A1B,59-DAP","biotype":"protein_coding","ncbi_id":"6641","summary":"Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]","start":120535745,"end":120813273,"strand":-1,"description":"syntrophin beta 1 [Source:HGNC Symbol;Acc:HGNC:11168]"}, {"versioned_ensembl_gene_id":"ENSG00000253279.5","gene_symbol":"LINC02209","gene_name":"long intergenic non-protein coding RNA 2209 [Source:HGNC Symbol;Acc:HGNC:27827]","synonyms":"FAM183CP","biotype":"lincRNA","ncbi_id":"286135","summary":null,"start":29921513,"end":29953724,"strand":1,"description":"long intergenic non-protein coding RNA 2209 [Source:HGNC Symbol;Acc:HGNC:27827]"}, {"versioned_ensembl_gene_id":"ENSG00000132357.13","gene_symbol":"CARD6","gene_name":"caspase recruitment domain family member 6 [Source:HGNC Symbol;Acc:HGNC:16394]","synonyms":"CINCIN1","biotype":"protein_coding","ncbi_id":"84674","summary":"This gene encodes a protein that contains a caspase recruitment domain (CARD), an antiparallel six-helical bundle that mediates homotypic protein-protein interactions. The encoded protein is a microtubule-associated protein that has been shown to interact with receptor-interacting protein kinases and positively modulate signal transduction pathways converging on activation of the inducible transcription factor NF-kB. [provided by RefSeq, Jul 2008]","start":40841184,"end":40860175,"strand":1,"description":"caspase recruitment domain family member 6 [Source:HGNC Symbol;Acc:HGNC:16394]"}, {"versioned_ensembl_gene_id":"ENSG00000178997.11","gene_symbol":"EXD1","gene_name":"exonuclease 3'-5' domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28507]","synonyms":"MGC33637,EXDL1","biotype":"protein_coding","ncbi_id":"161829","summary":null,"start":41182725,"end":41230743,"strand":-1,"description":"exonuclease 3'-5' domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28507]"}, {"versioned_ensembl_gene_id":"ENSG00000237058.1","gene_symbol":"AL831784.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2632568,"end":2636620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103642.11","gene_symbol":"LACTB","gene_name":"lactamase beta [Source:HGNC Symbol;Acc:HGNC:16468]","synonyms":"MRPL56,FLJ14902","biotype":"protein_coding","ncbi_id":"114294","summary":"This gene encodes a mitochondrially-localized protein that has sequence similarity to prokaryotic beta-lactamases. Many of the residues responsible for beta-lactamase activity are not conserved in this protein, suggesting it may have a different enzymatic function. Increased expression of the related mouse gene was found to be associated with obesity. Alternative splicing results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Dec 2013]","start":63121800,"end":63142061,"strand":1,"description":"lactamase beta [Source:HGNC Symbol;Acc:HGNC:16468]"}, {"versioned_ensembl_gene_id":"ENSG00000267039.1","gene_symbol":"AC016493.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36901946,"end":36923814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241166.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLAL,HLA92,HLA-92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30249873,"end":30257227,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000279753.1","gene_symbol":"AC011558.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1038727,"end":1039064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283138.1","gene_symbol":"AC006207.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3752518,"end":3757842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180694.13","gene_symbol":"TMEM64","gene_name":"transmembrane protein 64 [Source:HGNC Symbol;Acc:HGNC:25441]","synonyms":"DKFZp762C1112","biotype":"protein_coding","ncbi_id":"169200","summary":null,"start":90621995,"end":90791632,"strand":-1,"description":"transmembrane protein 64 [Source:HGNC Symbol;Acc:HGNC:25441]"}, {"versioned_ensembl_gene_id":"ENSG00000064655.18","gene_symbol":"EYA2","gene_name":"EYA transcriptional coactivator and phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3520]","synonyms":"EAB1","biotype":"protein_coding","ncbi_id":"2139","summary":"This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may be post-translationally modified and may play a role in eye development. A similar protein in mice can act as a transcriptional activator. Alternative splicing results in multiple transcript variants, but the full-length natures of all of these variants have not yet been determined. [provided by RefSeq, Jul 2009]","start":46894624,"end":47188844,"strand":1,"description":"EYA transcriptional coactivator and phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3520]"}, {"versioned_ensembl_gene_id":"ENSG00000272758.5","gene_symbol":"AC083798.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122416207,"end":122443180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203756.7","gene_symbol":"TMEM244","gene_name":"transmembrane protein 244 [Source:HGNC Symbol;Acc:HGNC:21571]","synonyms":"C6orf191,bA174C7.4","biotype":"protein_coding","ncbi_id":"253582","summary":null,"start":129831244,"end":129861547,"strand":-1,"description":"transmembrane protein 244 [Source:HGNC Symbol;Acc:HGNC:21571]"}, {"versioned_ensembl_gene_id":"ENSG00000243507.1","gene_symbol":"AC005908.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3468950,"end":3469296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224488.1","gene_symbol":"SAMM50P1","gene_name":"SAMM50 sorting and assembly machinery component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49778]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271893","summary":null,"start":17447145,"end":17448543,"strand":-1,"description":"SAMM50 sorting and assembly machinery component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49778]"}, {"versioned_ensembl_gene_id":"ENSG00000233740.1","gene_symbol":"CICP2","gene_name":"capicua transcriptional repressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360016","summary":null,"start":24278337,"end":24281140,"strand":-1,"description":"capicua transcriptional repressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23935]"}, {"versioned_ensembl_gene_id":"ENSG00000179409.10","gene_symbol":"GEMIN4","gene_name":"gem nuclear organelle associated protein 4 [Source:HGNC Symbol;Acc:HGNC:15717]","synonyms":"DKFZP434B131,p97,HHRF-1,HCAP1,HC56,DKFZP434D174","biotype":"protein_coding","ncbi_id":"50628","summary":"The product of this gene is part of a large complex localized to the cytoplasm, nucleoli, and to discrete nuclear bodies called Gemini bodies (gems). The complex functions in spliceosomal snRNP assembly in the cytoplasm, and regenerates spliceosomes required for pre-mRNA splicing in the nucleus. The encoded protein directly interacts with a DEAD box protein and several spliceosome core proteins. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":744414,"end":753999,"strand":-1,"description":"gem nuclear organelle associated protein 4 [Source:HGNC Symbol;Acc:HGNC:15717]"}, {"versioned_ensembl_gene_id":"ENSG00000239831.1","gene_symbol":"RNF7P1","gene_name":"ring finger protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43425]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506872","summary":null,"start":57519669,"end":57520010,"strand":-1,"description":"ring finger protein 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43425]"}, {"versioned_ensembl_gene_id":"ENSG00000105929.15","gene_symbol":"ATP6V0A4","gene_name":"ATPase H+ transporting V0 subunit a4 [Source:HGNC Symbol;Acc:HGNC:866]","synonyms":"VPP2,Vph1,Stv1,RTADR,RTA1C,RDRTA2,ATP6N2,ATP6N1B,a4","biotype":"protein_coding","ncbi_id":"50617","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. This gene is one of four genes in man and mouse that encode different isoforms of the a subunit. Alternatively spliced transcript variants encoding the same protein have been described. Mutations in this gene are associated with renal tubular acidosis associated with preserved hearing. [provided by RefSeq, Jul 2008]","start":138706295,"end":138799560,"strand":-1,"description":"ATPase H+ transporting V0 subunit a4 [Source:HGNC Symbol;Acc:HGNC:866]"}, {"versioned_ensembl_gene_id":"ENSG00000276518.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"protein_coding","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54771247,"end":54784650,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000280274.1","gene_symbol":"AC009145.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79016136,"end":79017429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261837.1","gene_symbol":"AC046158.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":78534374,"end":78535648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279887.1","gene_symbol":"AC046158.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78525189,"end":78526535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160961.11","gene_symbol":"ZNF333","gene_name":"zinc finger protein 333 [Source:HGNC Symbol;Acc:HGNC:15624]","synonyms":"KIAA1806","biotype":"protein_coding","ncbi_id":"84449","summary":null,"start":14689801,"end":14733746,"strand":1,"description":"zinc finger protein 333 [Source:HGNC Symbol;Acc:HGNC:15624]"}, {"versioned_ensembl_gene_id":"ENSG00000101144.12","gene_symbol":"BMP7","gene_name":"bone morphogenetic protein 7 [Source:HGNC Symbol;Acc:HGNC:1074]","synonyms":"OP-1","biotype":"protein_coding","ncbi_id":"655","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone, kidney and brown adipose tissue development. Additionally, this protein induces ectopic bone formation and may promote fracture healing in human patients. [provided by RefSeq, Jul 2016]","start":57168748,"end":57266629,"strand":-1,"description":"bone morphogenetic protein 7 [Source:HGNC Symbol;Acc:HGNC:1074]"}, {"versioned_ensembl_gene_id":"ENSG00000139515.5","gene_symbol":"PDX1","gene_name":"pancreatic and duodenal homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6107]","synonyms":"STF-1,PDX-1,MODY4,IPF1,IDX-1","biotype":"protein_coding","ncbi_id":"3651","summary":"The protein encoded by this gene is a transcriptional activator of several genes, including insulin, somatostatin, glucokinase, islet amyloid polypeptide, and glucose transporter type 2. The encoded nuclear protein is involved in the early development of the pancreas and plays a major role in glucose-dependent regulation of insulin gene expression. Defects in this gene are a cause of pancreatic agenesis, which can lead to early-onset insulin-dependent diabetes mellitus (IDDM), as well as maturity onset diabetes of the young type 4 (MODY4). [provided by RefSeq, Aug 2017]","start":27920020,"end":27926231,"strand":1,"description":"pancreatic and duodenal homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6107]"}, {"versioned_ensembl_gene_id":"ENSG00000219302.2","gene_symbol":"AL451046.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129819637,"end":129820170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282608.1","gene_symbol":"ADORA3","gene_name":"adenosine A3 receptor [Source:HGNC Symbol;Acc:HGNC:268]","synonyms":"AD026","biotype":"protein_coding","ncbi_id":"140","summary":"This gene encodes a protein that belongs to the family of adenosine receptors, which are G-protein-coupled receptors that are involved in a variety of intracellular signaling pathways and physiological functions. The receptor encoded by this gene mediates a sustained cardioprotective function during cardiac ischemia, it is involved in the inhibition of neutrophil degranulation in neutrophil-mediated tissue injury, it has been implicated in both neuroprotective and neurodegenerative effects, and it may also mediate both cell proliferation and cell death. Alternative splicing results in multiple transcript variants. This gene shares its 5' terminal exon with some transcripts from overlapping GeneID:57413, which encodes an immunoglobulin domain-containing protein. [provided by RefSeq, Nov 2014]","start":111499429,"end":111503760,"strand":-1,"description":"adenosine A3 receptor [Source:HGNC Symbol;Acc:HGNC:268]"}, {"versioned_ensembl_gene_id":"ENSG00000219666.2","gene_symbol":"AL451046.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129783769,"end":129784045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102048.15","gene_symbol":"ASB9","gene_name":"ankyrin repeat and SOCS box containing 9 [Source:HGNC Symbol;Acc:HGNC:17184]","synonyms":"MGC4954,FLJ20636,DKFZP564L0862","biotype":"protein_coding","ncbi_id":"140462","summary":"This gene encodes a member of the ankyrin repeat and suppressor of cytokine signaling (SOCS) box protein family. Members of this family can interact with the elongin B-C adapter complex via their SOCS box domain and further complex with the cullin and ring box proteins to form E3 ubiquitin ligase complexes. They may function to mediate the substrate-recognition of the E3 ubiquitin ligases. A transcribed pseudogene of this gene has been identified on chromosome 15. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":15235288,"end":15270467,"strand":-1,"description":"ankyrin repeat and SOCS box containing 9 [Source:HGNC Symbol;Acc:HGNC:17184]"}, {"versioned_ensembl_gene_id":"ENSG00000227388.2","gene_symbol":"AL133410.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35772163,"end":35790432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217416.4","gene_symbol":"ISCA1P1","gene_name":"iron-sulfur cluster assembly 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33263]","synonyms":"ISCA1L","biotype":"processed_pseudogene","ncbi_id":"389293","summary":null,"start":62776877,"end":62777263,"strand":-1,"description":"iron-sulfur cluster assembly 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33263]"}, {"versioned_ensembl_gene_id":"ENSG00000174844.14","gene_symbol":"DNAH12","gene_name":"dynein axonemal heavy chain 12 [Source:HGNC Symbol;Acc:HGNC:2943]","synonyms":"HL-19,hdhc3,FLJ44290,FLJ40427,DNHD2,Dnahc3,DNAH7L,DNAH12L,DLP12,DHC3","biotype":"protein_coding","ncbi_id":"201625","summary":null,"start":57293699,"end":57544344,"strand":-1,"description":"dynein axonemal heavy chain 12 [Source:HGNC Symbol;Acc:HGNC:2943]"}, {"versioned_ensembl_gene_id":"ENSG00000141034.9","gene_symbol":"GID4","gene_name":"GID complex subunit 4 homolog [Source:HGNC Symbol;Acc:HGNC:28453]","synonyms":"VID24,C17orf39","biotype":"protein_coding","ncbi_id":"79018","summary":"The multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":18039292,"end":18068404,"strand":1,"description":"GID complex subunit 4 homolog [Source:HGNC Symbol;Acc:HGNC:28453]"}, {"versioned_ensembl_gene_id":"ENSG00000204619.7","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"HCG-V,TCTE5,CFAP255,HCGV,Tctex5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30066709,"end":30070333,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000228452.1","gene_symbol":"AC098484.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42775813,"end":42776790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140285.9","gene_symbol":"FGF7","gene_name":"fibroblast growth factor 7 [Source:HGNC Symbol;Acc:HGNC:3685]","synonyms":"KGF","biotype":"protein_coding","ncbi_id":"2252","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is a potent epithelial cell-specific growth factor, whose mitogenic activity is predominantly exhibited in keratinocytes but not in fibroblasts and endothelial cells. Studies of mouse and rat homologs of this gene implicated roles in morphogenesis of epithelium, reepithelialization of wounds, hair development and early lung organogenesis. [provided by RefSeq, Jul 2008]","start":49423096,"end":49488775,"strand":1,"description":"fibroblast growth factor 7 [Source:HGNC Symbol;Acc:HGNC:3685]"}, {"versioned_ensembl_gene_id":"ENSG00000253855.1","gene_symbol":"AC245187.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2518998,"end":2522182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121871.3","gene_symbol":"SLITRK3","gene_name":"SLIT and NTRK like family member 3 [Source:HGNC Symbol;Acc:HGNC:23501]","synonyms":"KIAA0848","biotype":"protein_coding","ncbi_id":"22865","summary":"This gene encodes a member of the Slitrk family of structurally related transmembrane proteins that are involved in controlling neurite outgrowth. The encoded protein contains two leucine-rich repeat (LRR) domains and a C-terminal domain that is partially similar to Trk neurotrophin receptor protein. Enhanced expression of this gene was found in tissue from several different types of tumors. Alternative splicing results in multiple transcript variants, all encoding the same protein. [provided by RefSeq, Jan 2016]","start":165186720,"end":165197109,"strand":-1,"description":"SLIT and NTRK like family member 3 [Source:HGNC Symbol;Acc:HGNC:23501]"}, {"versioned_ensembl_gene_id":"ENSG00000235318.3","gene_symbol":"MTND4LP13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075100","summary":null,"start":201214653,"end":201214950,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42247]"}, {"versioned_ensembl_gene_id":"ENSG00000237875.1","gene_symbol":"AL353691.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41790192,"end":41790250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236274.1","gene_symbol":"AC004865.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35509742,"end":35511438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197372.9","gene_symbol":"ZNF675","gene_name":"zinc finger protein 675 [Source:HGNC Symbol;Acc:HGNC:30768]","synonyms":"TIZ,TBZF","biotype":"protein_coding","ncbi_id":"171392","summary":null,"start":23525631,"end":23687220,"strand":-1,"description":"zinc finger protein 675 [Source:HGNC Symbol;Acc:HGNC:30768]"}, {"versioned_ensembl_gene_id":"ENSG00000129071.9","gene_symbol":"MBD4","gene_name":"methyl-CpG binding domain 4, DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:6919]","synonyms":"MED1","biotype":"protein_coding","ncbi_id":"8930","summary":"The protein encoded by this gene is a member of a family of nuclear proteins related by the presence of a methyl-CpG binding domain (MBD). These proteins are capable of binding specifically to methylated DNA, and some members can also repress transcription from methylated gene promoters. This protein contains an MBD domain at the N-terminus that functions both in binding to methylated DNA and in protein interactions and a C-terminal mismatch-specific glycosylase domain that is involved in DNA repair. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013]","start":129430944,"end":129440179,"strand":-1,"description":"methyl-CpG binding domain 4, DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:6919]"}, {"versioned_ensembl_gene_id":"ENSG00000171241.8","gene_symbol":"SHCBP1","gene_name":"SHC binding and spindle associated 1 [Source:HGNC Symbol;Acc:HGNC:29547]","synonyms":"PAL,FLJ22009","biotype":"protein_coding","ncbi_id":"79801","summary":null,"start":46580554,"end":46621626,"strand":-1,"description":"SHC binding and spindle associated 1 [Source:HGNC Symbol;Acc:HGNC:29547]"}, {"versioned_ensembl_gene_id":"ENSG00000262845.7","gene_symbol":"KRT40","gene_name":"keratin 40 [Source:HGNC Symbol;Acc:HGNC:26707]","synonyms":"FLJ36600,KA36","biotype":"protein_coding","ncbi_id":"125115","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40977843,"end":40987262,"strand":-1,"description":"keratin 40 [Source:HGNC Symbol;Acc:HGNC:26707]"}, {"versioned_ensembl_gene_id":"ENSG00000260731.1","gene_symbol":"KRT8P22","gene_name":"keratin 8 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:33374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"342419","summary":null,"start":78048483,"end":78049897,"strand":-1,"description":"keratin 8 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:33374]"}, {"versioned_ensembl_gene_id":"ENSG00000228393.3","gene_symbol":"LINC01004","gene_name":"long intergenic non-protein coding RNA 1004 [Source:HGNC Symbol;Acc:HGNC:48961]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100216546","summary":null,"start":104950315,"end":105013044,"strand":-1,"description":"long intergenic non-protein coding RNA 1004 [Source:HGNC Symbol;Acc:HGNC:48961]"}, {"versioned_ensembl_gene_id":"ENSG00000163788.13","gene_symbol":"SNRK","gene_name":"SNF related kinase [Source:HGNC Symbol;Acc:HGNC:30598]","synonyms":"KIAA0096,HSNFRK,FLJ20224","biotype":"protein_coding","ncbi_id":"54861","summary":"SNRK is a member of the sucrose nonfermenting (SNF)-related kinase family of serine/threonine kinases (Kertesz et al., 2002 [PubMed 12234663]).[supplied by OMIM, Apr 2009]","start":43286512,"end":43424764,"strand":1,"description":"SNF related kinase [Source:HGNC Symbol;Acc:HGNC:30598]"}, {"versioned_ensembl_gene_id":"ENSG00000197959.13","gene_symbol":"DNM3","gene_name":"dynamin 3 [Source:HGNC Symbol;Acc:HGNC:29125]","synonyms":"KIAA0820","biotype":"protein_coding","ncbi_id":"26052","summary":"This gene encodes a member of a family of guanosine triphosphate (GTP)-binding proteins that associate with microtubules and are involved in vesicular transport. The encoded protein functions in the development of megakaryocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":171841498,"end":172418466,"strand":1,"description":"dynamin 3 [Source:HGNC Symbol;Acc:HGNC:29125]"}, {"versioned_ensembl_gene_id":"ENSG00000261776.1","gene_symbol":"AC079414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78055824,"end":78056927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123561.14","gene_symbol":"SERPINA7","gene_name":"serpin family A member 7 [Source:HGNC Symbol;Acc:HGNC:11583]","synonyms":"TBG","biotype":"protein_coding","ncbi_id":"6906","summary":"There are three proteins including thyroxine-binding globulin (TBG), transthyretin and albumin responsible for carrying the thyroid hormones thyroxine (T4) and 3,5,3'-triiodothyronine (T3) in the bloodstream. This gene encodes the major thyroid hormone transport protein, TBG, in serum. It belongs to the serpin family in genomics, but the protein has no inhibitory function like many other members of the serpin family. Mutations in this gene result in TGB deficiency, which has been classified as partial deficiency, complete deficiency, and excess, based on the level of serum TBG. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined.[provided by RefSeq, Jun 2012]","start":106032442,"end":106038738,"strand":-1,"description":"serpin family A member 7 [Source:HGNC Symbol;Acc:HGNC:11583]"}, {"versioned_ensembl_gene_id":"ENSG00000257048.1","gene_symbol":"LINC02417","gene_name":"long intergenic non-protein coding RNA 2417 [Source:HGNC Symbol;Acc:HGNC:53347]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101930162","summary":null,"start":3367833,"end":3371346,"strand":1,"description":"long intergenic non-protein coding RNA 2417 [Source:HGNC Symbol;Acc:HGNC:53347]"}, {"versioned_ensembl_gene_id":"ENSG00000253225.1","gene_symbol":"AC103833.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129250967,"end":129251138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253451.1","gene_symbol":"IGLV2-28","gene_name":"immunoglobulin lambda variable 2-28 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5891]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28812","summary":null,"start":22664473,"end":22664907,"strand":1,"description":"immunoglobulin lambda variable 2-28 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5891]"}, {"versioned_ensembl_gene_id":"ENSG00000147123.10","gene_symbol":"NDUFB11","gene_name":"NADH:ubiquinone oxidoreductase subunit B11 [Source:HGNC Symbol;Acc:HGNC:20372]","synonyms":"Np15,ESSS,NP17.3","biotype":"protein_coding","ncbi_id":"54539","summary":"The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to ubiquinone. Mutations in the human gene are associated with linear skin defects with multiple congenital anomalies 3 and mitochondrial complex I deficiency. [provided by RefSeq, Dec 2016]","start":47142216,"end":47145504,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B11 [Source:HGNC Symbol;Acc:HGNC:20372]"}, {"versioned_ensembl_gene_id":"ENSG00000116704.7","gene_symbol":"SLC35D1","gene_name":"solute carrier family 35 member D1 [Source:HGNC Symbol;Acc:HGNC:20800]","synonyms":"KIAA0260,UGTREL7","biotype":"protein_coding","ncbi_id":"23169","summary":"Glycosylation of cellular glycoconjugates occurs in the endoplasmic reticulum (ER) and Golgi compartment, and requires transport of nucleotide sugars from the cytosol into the lumen of the ER and Golgi by specific transporters. The protein encoded by this gene resides in the ER, and transports both UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylgalactosamine (UDP-GalNAc) from the cytoplasm to the ER lumen. It may participate in glucuronidation and/or chondroitin sulfate biosynthesis. Mutations in this gene are associated with Schneckenbecken dysplasia.[provided by RefSeq, Sep 2009]","start":66999332,"end":67054099,"strand":-1,"description":"solute carrier family 35 member D1 [Source:HGNC Symbol;Acc:HGNC:20800]"}, {"versioned_ensembl_gene_id":"ENSG00000223946.1","gene_symbol":"AL513008.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42030053,"end":42031382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284070.1","gene_symbol":"AP000356.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24645171,"end":24651657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000043514.15","gene_symbol":"TRIT1","gene_name":"tRNA isopentenyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:20286]","synonyms":"IPT,FLJ20061","biotype":"protein_coding","ncbi_id":"54802","summary":"This gene encodes a protein that that is targeted to the mitochondrion and modifies transfer RNAs (tRNAs) by adding a dimethylallyl group onto the adenine at position 37. This modification is important for maintaining the correct reading frame during protein translation. This gene is considered a tumor suppressor and its expression can decrease cell growth. Alternative splicing results in multiple transcripts variants, most of which are likely non-functional. [provided by RefSeq, Aug 2015]","start":39841022,"end":39883511,"strand":-1,"description":"tRNA isopentenyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:20286]"}, {"versioned_ensembl_gene_id":"ENSG00000183706.4","gene_symbol":"OR4N4","gene_name":"olfactory receptor family 4 subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:15375]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283694","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22094431,"end":22095556,"strand":1,"description":"olfactory receptor family 4 subfamily N member 4 [Source:HGNC Symbol;Acc:HGNC:15375]"}, {"versioned_ensembl_gene_id":"ENSG00000278662.4","gene_symbol":"GOLGA6L10","gene_name":"golgin A6 family-like 10 [Source:HGNC Symbol;Acc:HGNC:37228]","synonyms":"GOLGA6L18,GOLGA6L18","biotype":"protein_coding","ncbi_id":"647042","summary":null,"start":82339998,"end":82349475,"strand":-1,"description":"golgin A6 family-like 10 [Source:HGNC Symbol;Acc:HGNC:37228]"}, {"versioned_ensembl_gene_id":"ENSG00000213759.9","gene_symbol":"UGT2B11","gene_name":"UDP glucuronosyltransferase family 2 member B11 [Source:HGNC Symbol;Acc:HGNC:12545]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10720","summary":null,"start":69199951,"end":69214731,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B11 [Source:HGNC Symbol;Acc:HGNC:12545]"}, {"versioned_ensembl_gene_id":"ENSG00000116273.5","gene_symbol":"PHF13","gene_name":"PHD finger protein 13 [Source:HGNC Symbol;Acc:HGNC:22983]","synonyms":"MGC43399","biotype":"protein_coding","ncbi_id":"148479","summary":null,"start":6613685,"end":6624033,"strand":1,"description":"PHD finger protein 13 [Source:HGNC Symbol;Acc:HGNC:22983]"}, {"versioned_ensembl_gene_id":"ENSG00000157703.15","gene_symbol":"SVOPL","gene_name":"SVOP like [Source:HGNC Symbol;Acc:HGNC:27034]","synonyms":"MGC46715","biotype":"protein_coding","ncbi_id":"136306","summary":"The protein encoded by this gene is thought to be a member of solute carrier family 22, which includes transmembrane proteins that transport toxins and drugs from the body. This gene is a paralog of the SVOP gene that encodes synaptic vesicle 2-related protein. [provided by RefSeq, Sep 2016]","start":138594285,"end":138701352,"strand":-1,"description":"SVOP like [Source:HGNC Symbol;Acc:HGNC:27034]"}, {"versioned_ensembl_gene_id":"ENSG00000147885.4","gene_symbol":"IFNA16","gene_name":"interferon alpha 16 [Source:HGNC Symbol;Acc:HGNC:5421]","synonyms":"IFN-alphaO","biotype":"protein_coding","ncbi_id":"3449","summary":null,"start":21216373,"end":21217311,"strand":-1,"description":"interferon alpha 16 [Source:HGNC Symbol;Acc:HGNC:5421]"}, {"versioned_ensembl_gene_id":"ENSG00000234818.1","gene_symbol":"AC007314.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10589166,"end":10604830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188095.4","gene_symbol":"MESP2","gene_name":"mesoderm posterior bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29659]","synonyms":"SCDO2,bHLHc6","biotype":"protein_coding","ncbi_id":"145873","summary":"This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02). [provided by RefSeq, Oct 2008]","start":89760591,"end":89778754,"strand":1,"description":"mesoderm posterior bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:29659]"}, {"versioned_ensembl_gene_id":"ENSG00000159086.14","gene_symbol":"PAXBP1","gene_name":"PAX3 and PAX7 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13579]","synonyms":"C21orf66,GCFC1,GCFC,fSAP105","biotype":"protein_coding","ncbi_id":"94104","summary":"This gene encodes a protein that may bind to GC-rich DNA sequences, which suggests its involvement in the regulation of transcription. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2009]","start":32733899,"end":32771858,"strand":-1,"description":"PAX3 and PAX7 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13579]"}, {"versioned_ensembl_gene_id":"ENSG00000231699.1","gene_symbol":"AC020550.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197533803,"end":197533965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232281.2","gene_symbol":"IFNWP15","gene_name":"interferon omega 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:5449]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130866","summary":null,"start":21178589,"end":21179188,"strand":-1,"description":"interferon omega 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:5449]"}, {"versioned_ensembl_gene_id":"ENSG00000036828.15","gene_symbol":"CASR","gene_name":"calcium sensing receptor [Source:HGNC Symbol;Acc:HGNC:1514]","synonyms":"FHH,NSHPT,HHC1,HHC,GPRC2A","biotype":"protein_coding","ncbi_id":"846","summary":"The protein encoded by this gene is a plasma membrane G protein-coupled receptor that senses small changes in circulating calcium concentration. The encoded protein couples this information to intracellular signaling pathways that modify parathyroid hormone secretion or renal cation handling, and thus this protein plays an essential role in maintaining mineral ion homeostasis. Mutations in this gene are a cause of familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia. [provided by RefSeq, Aug 2017]","start":122183683,"end":122291629,"strand":1,"description":"calcium sensing receptor [Source:HGNC Symbol;Acc:HGNC:1514]"}, {"versioned_ensembl_gene_id":"ENSG00000009724.16","gene_symbol":"MASP2","gene_name":"mannan binding lectin serine peptidase 2 [Source:HGNC Symbol;Acc:HGNC:6902]","synonyms":"MASP1P1","biotype":"protein_coding","ncbi_id":"10747","summary":"This gene encodes a member of the peptidase S1 family of serine proteases. The encoded preproprotein is proteolytically processed to generate A and B chains that heterodimerize to form the mature protease. This protease cleaves complement components C2 and C4 in order to generate C3 convertase in the lectin pathway of the complement system. The encoded protease also plays a role in the coagulation cascade through cleavage of prothrombin to form thrombin. Myocardial infarction and acute stroke patients exhibit reduced serum concentrations of the encoded protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":11026523,"end":11047233,"strand":-1,"description":"mannan binding lectin serine peptidase 2 [Source:HGNC Symbol;Acc:HGNC:6902]"}, {"versioned_ensembl_gene_id":"ENSG00000147813.15","gene_symbol":"NAPRT","gene_name":"nicotinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30450]","synonyms":"PP3856,NAPRT1","biotype":"protein_coding","ncbi_id":"93100","summary":"Nicotinic acid (NA; niacin) is converted by nicotinic acid phosphoribosyltransferase (NAPRT; EC 2.4.2.11) to NA mononucleotide (NaMN), which is then converted to NA adenine dinucleotide (NaAD), and finally to nicotinamide adenine dinucleotide (NAD), which serves as a coenzyme in cellular redox reactions and is an essential component of a variety of processes in cellular metabolism including response to stress (Hara et al., 2007).[supplied by OMIM, Mar 2008]","start":143574785,"end":143578649,"strand":-1,"description":"nicotinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30450]"}, {"versioned_ensembl_gene_id":"ENSG00000127554.12","gene_symbol":"GFER","gene_name":"growth factor, augmenter of liver regeneration [Source:HGNC Symbol;Acc:HGNC:4236]","synonyms":"HSS,HPO2,HPO1,HERV1,ERV1,ALR","biotype":"protein_coding","ncbi_id":"2671","summary":"The hepatotrophic factor designated augmenter of liver regeneration (ALR) is thought to be one of the factors responsible for the extraordinary regenerative capacity of mammalian liver. It has also been called hepatic regenerative stimulation substance (HSS). The gene resides on chromosome 16 in the interval containing the locus for polycystic kidney disease (PKD1). The putative gene product is 42% similar to the scERV1 protein of yeast. The yeast scERV1 gene had been found to be essential for oxidative phosphorylation, the maintenance of mitochondrial genomes, and the cell division cycle. The human gene is both the structural and functional homolog of the yeast scERV1 gene. [provided by RefSeq, Jul 2008]","start":1984207,"end":1987749,"strand":1,"description":"growth factor, augmenter of liver regeneration [Source:HGNC Symbol;Acc:HGNC:4236]"}, {"versioned_ensembl_gene_id":"ENSG00000005469.11","gene_symbol":"CROT","gene_name":"carnitine O-octanoyltransferase [Source:HGNC Symbol;Acc:HGNC:2366]","synonyms":"COT","biotype":"protein_coding","ncbi_id":"54677","summary":"This gene encodes a member of the carnitine/choline acetyltransferase family. The encoded protein converts 4,8-dimethylnonanoyl-CoA to its corresponding carnitine ester. This transesterification occurs in the peroxisome and is necessary for transport of medium- and long- chain acyl-CoA molecules out of the peroxisome to the cytosol and mitochondria. The protein thus plays a role in lipid metabolism and fatty acid beta-oxidation. Alternatively spliced transcript variants have been described.[provided by RefSeq, Jan 2009]","start":87345681,"end":87399795,"strand":1,"description":"carnitine O-octanoyltransferase [Source:HGNC Symbol;Acc:HGNC:2366]"}, {"versioned_ensembl_gene_id":"ENSG00000162298.18","gene_symbol":"SYVN1","gene_name":"synoviolin 1 [Source:HGNC Symbol;Acc:HGNC:20738]","synonyms":"HRD1,DER3","biotype":"protein_coding","ncbi_id":"84447","summary":"This gene encodes a protein involved in endoplasmic reticulum (ER)-associated degradation. The encoded protein removes unfolded proteins, accumulated during ER stress, by retrograde transport to the cytosol from the ER. This protein also uses the ubiquitin-proteasome system for additional degradation of unfolded proteins. Sequence analysis identified two transcript variants that encode different isoforms. [provided by RefSeq, May 2011]","start":65121780,"end":65134533,"strand":-1,"description":"synoviolin 1 [Source:HGNC Symbol;Acc:HGNC:20738]"}, {"versioned_ensembl_gene_id":"ENSG00000113569.15","gene_symbol":"NUP155","gene_name":"nucleoporin 155 [Source:HGNC Symbol;Acc:HGNC:8063]","synonyms":"N155,KIAA0791","biotype":"protein_coding","ncbi_id":"9631","summary":"Nucleoporins are proteins that play an important role in the assembly and functioning of the nuclear pore complex (NPC) which regulates the movement of macromolecules across the nuclear envelope (NE). The protein encoded by this gene plays a role in the fusion of NE vesicles and formation of the double membrane NE. The protein may also be involved in cardiac physiology and may be associated with the pathogenesis of atrial fibrillation. Alternative splicing results in multiple transcript variants of this gene. A pseudogene associated with this gene is located on chromosome 6. [provided by RefSeq, May 2013]","start":37288137,"end":37371181,"strand":-1,"description":"nucleoporin 155 [Source:HGNC Symbol;Acc:HGNC:8063]"}, {"versioned_ensembl_gene_id":"ENSG00000254948.1","gene_symbol":"OR7E158P","gene_name":"olfactory receptor family 7 subfamily E member 158 pseudogene [Source:HGNC Symbol;Acc:HGNC:31232]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":11919900,"end":11920809,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 158 pseudogene [Source:HGNC Symbol;Acc:HGNC:31232]"}, {"versioned_ensembl_gene_id":"ENSG00000278355.4","gene_symbol":"LILRA5","gene_name":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]","synonyms":"CD85,LILRB7,ILT11,CD85f,LIR9","biotype":"protein_coding","ncbi_id":"353514","summary":"The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":54314055,"end":54320118,"strand":-1,"description":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]"}, {"versioned_ensembl_gene_id":"ENSG00000132199.18","gene_symbol":"ENOSF1","gene_name":"enolase superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:30365]","synonyms":"TYMSAS,rTS,HSRTSBETA","biotype":"protein_coding","ncbi_id":"55556","summary":"This gene can encode a mitochondrial enzyme that is thought to convert L-fuconate to 2-keto-3-deoxy-L-fuconate. This locus was originally identified as the source of antisense RNAs of the adjacent thymidylate synthase gene. Splice variants at this locus may contain an alternate 3' exon that is complementary to the 3'UTR and terminal intron of the thymidylate synthase (TS) RNA and may downregulate TS expression. [provided by RefSeq, Aug 2017]","start":670324,"end":712676,"strand":-1,"description":"enolase superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:30365]"}, {"versioned_ensembl_gene_id":"ENSG00000227911.3","gene_symbol":"LINC02344","gene_name":"long intergenic non-protein coding RNA 2344 [Source:HGNC Symbol;Acc:HGNC:53264]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370154","summary":null,"start":33333679,"end":33335277,"strand":-1,"description":"long intergenic non-protein coding RNA 2344 [Source:HGNC Symbol;Acc:HGNC:53264]"}, {"versioned_ensembl_gene_id":"ENSG00000244176.1","gene_symbol":"AP003733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62011751,"end":62012602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125977.6","gene_symbol":"EIF2S2","gene_name":"eukaryotic translation initiation factor 2 subunit beta [Source:HGNC Symbol;Acc:HGNC:3266]","synonyms":"EIF2,PPP1R67,EIF2beta","biotype":"protein_coding","ncbi_id":"8894","summary":"Eukaryotic translation initiation factor 2 (EIF-2) functions in the early steps of protein synthesis by forming a ternary complex with GTP and initiator tRNA and binding to a 40S ribosomal subunit. EIF-2 is composed of three subunits, alpha, beta, and gamma, with the protein encoded by this gene representing the beta subunit. The beta subunit catalyzes the exchange of GDP for GTP, which recycles the EIF-2 complex for another round of initiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":34088298,"end":34112332,"strand":-1,"description":"eukaryotic translation initiation factor 2 subunit beta [Source:HGNC Symbol;Acc:HGNC:3266]"}, {"versioned_ensembl_gene_id":"ENSG00000266824.1","gene_symbol":"AC129492.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8176812,"end":8182812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228913.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29552212,"end":29556525,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000163961.4","gene_symbol":"RNF168","gene_name":"ring finger protein 168 [Source:HGNC Symbol;Acc:HGNC:26661]","synonyms":"FLJ35794","biotype":"protein_coding","ncbi_id":"165918","summary":"This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome. [provided by RefSeq, Sep 2011]","start":196468783,"end":196503768,"strand":-1,"description":"ring finger protein 168 [Source:HGNC Symbol;Acc:HGNC:26661]"}, {"versioned_ensembl_gene_id":"ENSG00000280198.1","gene_symbol":"AC087163.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18026072,"end":18026771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187626.8","gene_symbol":"ZKSCAN4","gene_name":"zinc finger with KRAB and SCAN domains 4 [Source:HGNC Symbol;Acc:HGNC:13854]","synonyms":"ZSCAN36,ZNF427,ZNF307,p373c6.1,P1P373C6,FLJ32136","biotype":"protein_coding","ncbi_id":"387032","summary":null,"start":28244623,"end":28252224,"strand":-1,"description":"zinc finger with KRAB and SCAN domains 4 [Source:HGNC Symbol;Acc:HGNC:13854]"}, {"versioned_ensembl_gene_id":"ENSG00000267072.2","gene_symbol":"NAGPA-AS1","gene_name":"NAGPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44184]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507589","summary":null,"start":5010909,"end":5043999,"strand":1,"description":"NAGPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44184]"}, {"versioned_ensembl_gene_id":"ENSG00000226827.1","gene_symbol":"NPM1P11","gene_name":"nucleophosmin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:7913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10836","summary":null,"start":11257681,"end":11258535,"strand":-1,"description":"nucleophosmin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:7913]"}, {"versioned_ensembl_gene_id":"ENSG00000121579.12","gene_symbol":"NAA50","gene_name":"N(alpha)-acetyltransferase 50, NatE catalytic subunit [Source:HGNC Symbol;Acc:HGNC:29533]","synonyms":"San,NAT5,NAT13,MAK3,FLJ13194","biotype":"protein_coding","ncbi_id":"80218","summary":null,"start":113716460,"end":113746300,"strand":-1,"description":"N(alpha)-acetyltransferase 50, NatE catalytic subunit [Source:HGNC Symbol;Acc:HGNC:29533]"}, {"versioned_ensembl_gene_id":"ENSG00000260001.6","gene_symbol":"TGFBR3L","gene_name":"transforming growth factor beta receptor 3 like [Source:HGNC Symbol;Acc:HGNC:44152]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507588","summary":null,"start":7916145,"end":7919097,"strand":1,"description":"transforming growth factor beta receptor 3 like [Source:HGNC Symbol;Acc:HGNC:44152]"}, {"versioned_ensembl_gene_id":"ENSG00000274882.4","gene_symbol":"LINC02109","gene_name":"long intergenic non-protein coding RNA 2109 [Source:HGNC Symbol;Acc:HGNC:52964]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929660","summary":null,"start":29152383,"end":29181238,"strand":1,"description":"long intergenic non-protein coding RNA 2109 [Source:HGNC Symbol;Acc:HGNC:52964]"}, {"versioned_ensembl_gene_id":"ENSG00000281349.1","gene_symbol":"AC093627.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178225,"end":179318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214765.8","gene_symbol":"SEPT7P2","gene_name":"septin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32339]","synonyms":"SEPT7B,SEPT13,DKFZp313J1114","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"641977","summary":"Septins, such as SEPT13, are conserved GTP-binding proteins that function as dynamic, regulatable scaffolds for the recruitment of other proteins. They are involved in membrane dynamics, vesicle trafficking, apoptosis, and cytoskeleton remodeling, as well as infection, neurodegeneration, and neoplasia (Hall et al., 2005 [PubMed 15915442]).[supplied by OMIM, Jul 2008]","start":45723780,"end":45768985,"strand":-1,"description":"septin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32339]"}, {"versioned_ensembl_gene_id":"ENSG00000217089.1","gene_symbol":"RPS29P13","gene_name":"ribosomal protein S29 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271122","summary":null,"start":117048670,"end":117048838,"strand":-1,"description":"ribosomal protein S29 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35818]"}, {"versioned_ensembl_gene_id":"ENSG00000219559.1","gene_symbol":"AL512430.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110562175,"end":110562615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237467.1","gene_symbol":"USP9YP35","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:38779]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480719","summary":null,"start":24077799,"end":24079812,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:38779]"}, {"versioned_ensembl_gene_id":"ENSG00000258627.1","gene_symbol":"AC103996.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":93825058,"end":93825159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260188.1","gene_symbol":"AC002464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110477907,"end":110479436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237730.1","gene_symbol":"AC078991.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6422092,"end":6422701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259724.1","gene_symbol":"LINC01581","gene_name":"long intergenic non-protein coding RNA 1581 [Source:HGNC Symbol;Acc:HGNC:51415]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927112","summary":null,"start":93905405,"end":94107938,"strand":-1,"description":"long intergenic non-protein coding RNA 1581 [Source:HGNC Symbol;Acc:HGNC:51415]"}, {"versioned_ensembl_gene_id":"ENSG00000231375.1","gene_symbol":"CDY17P","gene_name":"chromodomain Y-linked 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:23861]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386739","summary":null,"start":24049878,"end":24051487,"strand":-1,"description":"chromodomain Y-linked 17 pseudogene [Source:HGNC Symbol;Acc:HGNC:23861]"}, {"versioned_ensembl_gene_id":"ENSG00000271118.1","gene_symbol":"AC012119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23805933,"end":23806154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269543.5","gene_symbol":"AC074135.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23068473,"end":23071476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230563.2","gene_symbol":"AL121757.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5471207,"end":5475182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109519.12","gene_symbol":"GRPEL1","gene_name":"GrpE like 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:19696]","synonyms":"hMGE,GrpE,FLJ25609","biotype":"protein_coding","ncbi_id":"80273","summary":null,"start":7058906,"end":7068197,"strand":-1,"description":"GrpE like 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:19696]"}, {"versioned_ensembl_gene_id":"ENSG00000217258.2","gene_symbol":"AC007249.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10452319,"end":10455552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255173.1","gene_symbol":"AP003068.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65117157,"end":65117458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179133.12","gene_symbol":"C10orf67","gene_name":"chromosome 10 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:28716]","synonyms":"MGC46732,LINC01552,C10orf115,bA215C7.4","biotype":"protein_coding","ncbi_id":"256815","summary":null,"start":23201916,"end":23344845,"strand":-1,"description":"chromosome 10 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:28716]"}, {"versioned_ensembl_gene_id":"ENSG00000129255.15","gene_symbol":"MPDU1","gene_name":"mannose-P-dolichol utilization defect 1 [Source:HGNC Symbol;Acc:HGNC:7207]","synonyms":"SL15,PQLC5,Lec35,CDGIf","biotype":"protein_coding","ncbi_id":"9526","summary":"This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":7583529,"end":7592789,"strand":1,"description":"mannose-P-dolichol utilization defect 1 [Source:HGNC Symbol;Acc:HGNC:7207]"}, {"versioned_ensembl_gene_id":"ENSG00000271661.1","gene_symbol":"BNIP3P36","gene_name":"BCL2 interacting protein 3 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:49716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481696","summary":null,"start":22994968,"end":22995847,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:49716]"}, {"versioned_ensembl_gene_id":"ENSG00000109674.3","gene_symbol":"NEIL3","gene_name":"nei like DNA glycosylase 3 [Source:HGNC Symbol;Acc:HGNC:24573]","synonyms":"hFPG2,FPG2,FLJ10858,ZGRF3,hNEI3","biotype":"protein_coding","ncbi_id":"55247","summary":"NEIL3 belongs to a class of DNA glycosylases homologous to the bacterial Fpg/Nei family. These glycosylases initiate the first step in base excision repair by cleaving bases damaged by reactive oxygen species and introducing a DNA strand break via the associated lyase reaction (Bandaru et al., 2002 [PubMed 12509226]).[supplied by OMIM, Mar 2008]","start":177309836,"end":177362943,"strand":1,"description":"nei like DNA glycosylase 3 [Source:HGNC Symbol;Acc:HGNC:24573]"}, {"versioned_ensembl_gene_id":"ENSG00000268104.2","gene_symbol":"SLC6A14","gene_name":"solute carrier family 6 member 14 [Source:HGNC Symbol;Acc:HGNC:11047]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11254","summary":"This gene encodes a member of the solute carrier family 6. Members of this family are sodium and chloride dependent neurotransmitter transporters. The encoded protein transports both neutral and cationic amino acids. This protein may also function as a beta-alanine carrier. Mutations in this gene may be associated with X-linked obesity. A pseudogene of this gene is found on chromosome X.[provided by RefSeq, May 2010]","start":116436622,"end":116461458,"strand":1,"description":"solute carrier family 6 member 14 [Source:HGNC Symbol;Acc:HGNC:11047]"}, {"versioned_ensembl_gene_id":"ENSG00000275985.1","gene_symbol":"ANKRD30BP3","gene_name":"ankyrin repeat domain 30B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27873]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338579","summary":null,"start":45176724,"end":45176925,"strand":1,"description":"ankyrin repeat domain 30B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27873]"}, {"versioned_ensembl_gene_id":"ENSG00000278121.1","gene_symbol":"AL512324.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45181082,"end":45181427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230060.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"NG31,C6orf25,G6b-B,G6b","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31706001,"end":31714117,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000173662.20","gene_symbol":"TAS1R1","gene_name":"taste 1 receptor member 1 [Source:HGNC Symbol;Acc:HGNC:14448]","synonyms":"TR1,T1R1,GPR70","biotype":"protein_coding","ncbi_id":"80835","summary":"The protein encoded by this gene is a G protein-coupled receptor and is a component of the heterodimeric amino acid taste receptor T1R1+3. The T1R1+3 receptor responds to L-amino acids but not to D-enantiomers or other compounds. Most amino acids that are perceived as sweet activate T1R1+3, and this activation is strictly dependent on an intact T1R1+3 heterodimer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":6555181,"end":6579757,"strand":1,"description":"taste 1 receptor member 1 [Source:HGNC Symbol;Acc:HGNC:14448]"}, {"versioned_ensembl_gene_id":"ENSG00000152782.16","gene_symbol":"PANK1","gene_name":"pantothenate kinase 1 [Source:HGNC Symbol;Acc:HGNC:8598]","synonyms":"MGC24596,PANK1b,PANK1a,PANK","biotype":"protein_coding","ncbi_id":"53354","summary":"This gene encodes a member of the pantothenate kinase family. Pantothenate kinases are key regulatory enzymes in the biosynthesis of coenzyme A (CoA). The encoded protein catalyzes the first and rate-limiting enzymatic reaction in CoA biosynthesis and is regulated by CoA through feedback inhibition. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. This gene and an intronic miRNA on the same strand are co-regulated by the tumor suppressor p53 (see PMID 20833636). [provided by RefSeq, Apr 2011]","start":89579497,"end":89645572,"strand":-1,"description":"pantothenate kinase 1 [Source:HGNC Symbol;Acc:HGNC:8598]"}, {"versioned_ensembl_gene_id":"ENSG00000261036.1","gene_symbol":"AC113418.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120345907,"end":120404837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258826.5","gene_symbol":"AL157955.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88018605,"end":88036319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223821.1","gene_symbol":"AL603910.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73492025,"end":73492742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151012.13","gene_symbol":"SLC7A11","gene_name":"solute carrier family 7 member 11 [Source:HGNC Symbol;Acc:HGNC:11059]","synonyms":"xCT","biotype":"protein_coding","ncbi_id":"23657","summary":"This gene encodes a member of a heteromeric, sodium-independent, anionic amino acid transport system that is highly specific for cysteine and glutamate. In this system, designated Xc(-), the anionic form of cysteine is transported in exchange for glutamate. This protein has been identified as the predominant mediator of Kaposi sarcoma-associated herpesvirus fusion and entry permissiveness into cells. Also, increased expression of this gene in primary gliomas (compared to normal brain tissue) was associated with increased glutamate secretion via the XCT channels, resulting in neuronal cell death. [provided by RefSeq, Sep 2011]","start":138164097,"end":138242349,"strand":-1,"description":"solute carrier family 7 member 11 [Source:HGNC Symbol;Acc:HGNC:11059]"}, {"versioned_ensembl_gene_id":"ENSG00000100354.20","gene_symbol":"TNRC6B","gene_name":"trinucleotide repeat containing 6B [Source:HGNC Symbol;Acc:HGNC:29190]","synonyms":"KIAA1093","biotype":"protein_coding","ncbi_id":"23112","summary":null,"start":40044817,"end":40335808,"strand":1,"description":"trinucleotide repeat containing 6B [Source:HGNC Symbol;Acc:HGNC:29190]"}, {"versioned_ensembl_gene_id":"ENSG00000227143.1","gene_symbol":"LINC01153","gene_name":"long intergenic non-protein coding RNA 1153 [Source:HGNC Symbol;Acc:HGNC:49495]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927889","summary":null,"start":121178700,"end":121185966,"strand":1,"description":"long intergenic non-protein coding RNA 1153 [Source:HGNC Symbol;Acc:HGNC:49495]"}, {"versioned_ensembl_gene_id":"ENSG00000243636.1","gene_symbol":"AL445493.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":207179296,"end":207184062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259476.1","gene_symbol":"AC018904.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58521311,"end":58523371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250074.1","gene_symbol":"AC006499.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10267895,"end":10268231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006555.10","gene_symbol":"TTC22","gene_name":"tetratricopeptide repeat domain 22 [Source:HGNC Symbol;Acc:HGNC:26067]","synonyms":"FLJ20619","biotype":"protein_coding","ncbi_id":"55001","summary":"This gene encodes a protein with seven tetratricopeptide (TPR) repeats. Tetratricopeptide repeat containing motifs are found in a variety of proteins and may mediate protein-protein interactions and chaperone activity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011]","start":54779712,"end":54801267,"strand":-1,"description":"tetratricopeptide repeat domain 22 [Source:HGNC Symbol;Acc:HGNC:26067]"}, {"versioned_ensembl_gene_id":"ENSG00000224695.1","gene_symbol":"MTND6P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39470]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478945","summary":null,"start":82817538,"end":82818061,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39470]"}, {"versioned_ensembl_gene_id":"ENSG00000197446.8","gene_symbol":"CYP2F1","gene_name":"cytochrome P450 family 2 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:2632]","synonyms":"CYP2F","biotype":"protein_coding","ncbi_id":"1572","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to dehydrogenate 3-methylindole, an endogenous toxin derived from the fermentation of tryptophan, as well as xenobiotic substrates such as naphthalene and ethoxycoumarin. This gene is part of a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. [provided by RefSeq, Jul 2008]","start":41114432,"end":41128366,"strand":1,"description":"cytochrome P450 family 2 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:2632]"}, {"versioned_ensembl_gene_id":"ENSG00000260564.1","gene_symbol":"AL161912.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79889001,"end":79892007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242125.3","gene_symbol":"SNHG3","gene_name":"small nucleolar RNA host gene 3 [Source:HGNC Symbol;Acc:HGNC:10118]","synonyms":"U17HG-A,U17HG,RNU17D,RNU17C,NCRNA00014","biotype":"sense_intronic","ncbi_id":"8420","summary":null,"start":28505980,"end":28510892,"strand":1,"description":"small nucleolar RNA host gene 3 [Source:HGNC Symbol;Acc:HGNC:10118]"}, {"versioned_ensembl_gene_id":"ENSG00000136935.13","gene_symbol":"GOLGA1","gene_name":"golgin A1 [Source:HGNC Symbol;Acc:HGNC:4424]","synonyms":"MGC33154,golgin-97","biotype":"protein_coding","ncbi_id":"2800","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This encoded protein is associated with Sjogren's syndrome. [provided by RefSeq, Feb 2010]","start":124878357,"end":124948492,"strand":-1,"description":"golgin A1 [Source:HGNC Symbol;Acc:HGNC:4424]"}, {"versioned_ensembl_gene_id":"ENSG00000135175.5","gene_symbol":"OCM2","gene_name":"oncomodulin 2 [Source:HGNC Symbol;Acc:HGNC:34396]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4951","summary":"This gene is similar to the oncomodulin gene, a high-affinity calcium ion-binding protein that belongs to the superfamily of calmodulin proteins, also known as the EF-hand proteins. [provided by RefSeq, Jul 2008]","start":97984684,"end":97991169,"strand":-1,"description":"oncomodulin 2 [Source:HGNC Symbol;Acc:HGNC:34396]"}, {"versioned_ensembl_gene_id":"ENSG00000143156.13","gene_symbol":"NME7","gene_name":"NME/NM23 family member 7 [Source:HGNC Symbol;Acc:HGNC:20461]","synonyms":"NM23-H7,FLJ37194,CFAP67","biotype":"protein_coding","ncbi_id":"29922","summary":"This gene encodes a member of the non-metastatic expressed family of nucleoside diphosphate kinases. Members of this family are enzymes that catalyzes phosphate transfer from nucleoside triphosphates to nucleoside diphosphates. This protein contains two kinase domains, one of which is involved in autophosphorylation and the other may be inactive. This protein localizes to the centrosome and functions as a component of the gamma-tubulin ring complex which plays a role in microtubule organization. Mutations in this gene may be associated with venous thromboembolism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":169132531,"end":169367967,"strand":-1,"description":"NME/NM23 family member 7 [Source:HGNC Symbol;Acc:HGNC:20461]"}, {"versioned_ensembl_gene_id":"ENSG00000154198.14","gene_symbol":"CYP4Z2P","gene_name":"cytochrome P450 family 4 subfamily Z member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:24426]","synonyms":"FLJ40054","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"163720","summary":null,"start":46843095,"end":46900437,"strand":-1,"description":"cytochrome P450 family 4 subfamily Z member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:24426]"}, {"versioned_ensembl_gene_id":"ENSG00000167920.8","gene_symbol":"TMEM99","gene_name":"transmembrane protein 99 [Source:HGNC Symbol;Acc:HGNC:28305]","synonyms":"MGC21518","biotype":"protein_coding","ncbi_id":"147184","summary":null,"start":40819106,"end":40836274,"strand":1,"description":"transmembrane protein 99 [Source:HGNC Symbol;Acc:HGNC:28305]"}, {"versioned_ensembl_gene_id":"ENSG00000113810.15","gene_symbol":"SMC4","gene_name":"structural maintenance of chromosomes 4 [Source:HGNC Symbol;Acc:HGNC:14013]","synonyms":"SMC4L1,hCAP-C,CAP-C","biotype":"protein_coding","ncbi_id":"10051","summary":"This gene belongs to the 'structural maintenance of chromosomes' (SMC) gene family. Members of this gene family play a role in two changes in chromosome structure during mitotic segregation of chromosomes- chromosome condensation and sister chromatid cohesion. The protein encoded by this gene is likely a subunit of the 13S condensin complex, which is involved in chromosome condensation. A pseudogene related to this gene is located on chromosome 2. [provided by RefSeq, Jun 2016]","start":160399274,"end":160434962,"strand":1,"description":"structural maintenance of chromosomes 4 [Source:HGNC Symbol;Acc:HGNC:14013]"}, {"versioned_ensembl_gene_id":"ENSG00000267659.5","gene_symbol":"LINC01482","gene_name":"long intergenic non-protein coding RNA 1482 [Source:HGNC Symbol;Acc:HGNC:51128]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928104","summary":null,"start":68591796,"end":68763882,"strand":1,"description":"long intergenic non-protein coding RNA 1482 [Source:HGNC Symbol;Acc:HGNC:51128]"}, {"versioned_ensembl_gene_id":"ENSG00000211445.11","gene_symbol":"GPX3","gene_name":"glutathione peroxidase 3 [Source:HGNC Symbol;Acc:HGNC:4555]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2878","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is secreted, and is abundantly found in plasma. Downregulation of expression of this gene by promoter hypermethylation has been observed in a wide spectrum of human malignancies, including thyroid cancer, hepatocellular carcinoma and chronic myeloid leukemia. This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2016]","start":151020438,"end":151028993,"strand":1,"description":"glutathione peroxidase 3 [Source:HGNC Symbol;Acc:HGNC:4555]"}, {"versioned_ensembl_gene_id":"ENSG00000213801.4","gene_symbol":"ZNF321P","gene_name":"zinc finger protein 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:13827]","synonyms":"MGC35402,ZNF321","biotype":"transcribed_processed_pseudogene","ncbi_id":"399669","summary":null,"start":52927135,"end":52942601,"strand":-1,"description":"zinc finger protein 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:13827]"}, {"versioned_ensembl_gene_id":"ENSG00000255387.1","gene_symbol":"AC015689.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4210354,"end":4212091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279530.2","gene_symbol":"AC092881.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70321542,"end":70324274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257139.1","gene_symbol":"AC084032.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70180338,"end":70202004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274445.1","gene_symbol":"AC006986.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9868462,"end":9868702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269526.1","gene_symbol":"ERVV-1","gene_name":"endogenous retrovirus group V member 1, envelope [Source:HGNC Symbol;Acc:HGNC:26501]","synonyms":"HERV-V1,FLJ32214,ENVV1","biotype":"protein_coding","ncbi_id":"147664","summary":"Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on human chromosome 19 that has inactivating mutations in the gag and pol genes. The gene's envelope protein is expressed in the human placenta but is truncated at its C-terminus. [provided by RefSeq, Oct 2015]","start":53013921,"end":53016122,"strand":1,"description":"endogenous retrovirus group V member 1, envelope [Source:HGNC Symbol;Acc:HGNC:26501]"}, {"versioned_ensembl_gene_id":"ENSG00000151690.14","gene_symbol":"MFSD6","gene_name":"major facilitator superfamily domain containing 6 [Source:HGNC Symbol;Acc:HGNC:24711]","synonyms":"FLJ20160","biotype":"protein_coding","ncbi_id":"54842","summary":null,"start":190408355,"end":190509205,"strand":1,"description":"major facilitator superfamily domain containing 6 [Source:HGNC Symbol;Acc:HGNC:24711]"}, {"versioned_ensembl_gene_id":"ENSG00000231513.3","gene_symbol":"E2F6P4","gene_name":"E2F transcription factor 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51452]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139542","summary":null,"start":136097835,"end":136098348,"strand":-1,"description":"E2F transcription factor 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51452]"}, {"versioned_ensembl_gene_id":"ENSG00000237061.1","gene_symbol":"AC100823.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73083787,"end":73085879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269646.1","gene_symbol":"AC010487.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52923382,"end":52924075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198932.12","gene_symbol":"GPRASP1","gene_name":"G protein-coupled receptor associated sorting protein 1 [Source:HGNC Symbol;Acc:HGNC:24834]","synonyms":"GASP1,GASP","biotype":"protein_coding","ncbi_id":"9737","summary":"This gene encodes a member of the GPRASP (G protein-coupled receptor associated sorting protein) family. The protein may modulate lysosomal sorting and functional down-regulation of a variety of G-protein coupled receptors. It targets receptors for degradation in lysosomes. The receptors interacting with this sorting protein include D2 dopamine receptor (DRD2), delta opioid receptor (OPRD1), beta-2 adrenergic receptor (ADRB2), D4 dopamine receptor (DRD4) and cannabinoid 1 receptor (CB1R). Multiple alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, May 2010]","start":102651366,"end":102659083,"strand":1,"description":"G protein-coupled receptor associated sorting protein 1 [Source:HGNC Symbol;Acc:HGNC:24834]"}, {"versioned_ensembl_gene_id":"ENSG00000278368.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816432,"end":54830744,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000108828.15","gene_symbol":"VAT1","gene_name":"vesicle amine transport 1 [Source:HGNC Symbol;Acc:HGNC:16919]","synonyms":"VATI,FLJ20230","biotype":"protein_coding","ncbi_id":"10493","summary":"Synaptic vesicles are responsible for regulating the storage and release of neurotransmitters in the nerve terminal. The protein encoded by this gene is an abundant integral membrane protein of cholinergic synaptic vesicles and is thought to be involved in vesicular transport. It belongs to the quinone oxidoreductase subfamily of zinc-containing alcohol dehydrogenase proteins. [provided by RefSeq, Jul 2008]","start":43014605,"end":43025123,"strand":-1,"description":"vesicle amine transport 1 [Source:HGNC Symbol;Acc:HGNC:16919]"}, {"versioned_ensembl_gene_id":"ENSG00000120802.13","gene_symbol":"TMPO","gene_name":"thymopoietin [Source:HGNC Symbol;Acc:HGNC:11875]","synonyms":"TP,LEMD4,LAP2","biotype":"protein_coding","ncbi_id":"7112","summary":"Through alternative splicing, this gene encodes several distinct LEM domain containing protein isoforms. LEM domain proteins include inner nuclear membrane and intranuclear proteins, and are involved in a variety of cellular functions including gene expression, chromatin organization, and replication and cell cycle control. The encoded alpha isoform is broadly diffuse in the nucleus and contains a lamin binding domain, while the beta and gamma isoforms are localized to the nuclear membrane and contain an HDAC3 interaction domain. The distinct isoforms may compete with each other when acting to chaperone other proteins and regulate transcription. [provided by RefSeq, Aug 2019]","start":98515512,"end":98550379,"strand":1,"description":"thymopoietin [Source:HGNC Symbol;Acc:HGNC:11875]"}, {"versioned_ensembl_gene_id":"ENSG00000130821.15","gene_symbol":"SLC6A8","gene_name":"solute carrier family 6 member 8 [Source:HGNC Symbol;Acc:HGNC:11055]","synonyms":"CT1,CRTR","biotype":"protein_coding","ncbi_id":"6535","summary":"The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":153688099,"end":153696593,"strand":1,"description":"solute carrier family 6 member 8 [Source:HGNC Symbol;Acc:HGNC:11055]"}, {"versioned_ensembl_gene_id":"ENSG00000257167.2","gene_symbol":"TMPO-AS1","gene_name":"TMPO antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44158]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128191","summary":null,"start":98512973,"end":98516422,"strand":-1,"description":"TMPO antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44158]"}, {"versioned_ensembl_gene_id":"ENSG00000276465.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832686,"end":54848263,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000245017.2","gene_symbol":"LINC02453","gene_name":"long intergenic non-protein coding RNA 2453 [Source:HGNC Symbol;Acc:HGNC:53392]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643770","summary":null,"start":98485544,"end":98503855,"strand":-1,"description":"long intergenic non-protein coding RNA 2453 [Source:HGNC Symbol;Acc:HGNC:53392]"}, {"versioned_ensembl_gene_id":"ENSG00000225827.1","gene_symbol":"SFTPA3P","gene_name":"surfactant protein A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10800]","synonyms":"SFTPAP1,COLEC6,SFTPP1","biotype":"processed_pseudogene","ncbi_id":"100288405","summary":null,"start":79595294,"end":79595660,"strand":-1,"description":"surfactant protein A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:10800]"}, {"versioned_ensembl_gene_id":"ENSG00000279504.1","gene_symbol":"AD001527.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36114362,"end":36115146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273999.1","gene_symbol":"RBM17P2","gene_name":"RNA binding motif protein 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50367]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642389","summary":null,"start":67211663,"end":67213067,"strand":-1,"description":"RNA binding motif protein 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50367]"}, {"versioned_ensembl_gene_id":"ENSG00000182481.8","gene_symbol":"KPNA2","gene_name":"karyopherin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6395]","synonyms":"SRP1alpha,RCH1,QIP2,IPOA1","biotype":"protein_coding","ncbi_id":"3838","summary":"The import of proteins into the nucleus is a process that involves at least 2 steps. The first is an energy-independent docking of the protein to the nuclear envelope and the second is an energy-dependent translocation through the nuclear pore complex. Imported proteins require a nuclear localization sequence (NLS) which generally consists of a short region of basic amino acids or 2 such regions spaced about 10 amino acids apart. Proteins involved in the first step of nuclear import have been identified in different systems. These include the Xenopus protein importin and its yeast homolog, SRP1 (a suppressor of certain temperature-sensitive mutations of RNA polymerase I in Saccharomyces cerevisiae), which bind to the NLS. KPNA2 protein interacts with the NLSs of DNA helicase Q1 and SV40 T antigen and may be involved in the nuclear transport of proteins. KPNA2 also may play a role in V(D)J recombination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":68035519,"end":68046842,"strand":1,"description":"karyopherin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6395]"}, {"versioned_ensembl_gene_id":"ENSG00000259978.1","gene_symbol":"MRPS21P8","gene_name":"mitochondrial ribosomal protein S21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:29755]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"350297","summary":null,"start":49764454,"end":49764688,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:29755]"}, {"versioned_ensembl_gene_id":"ENSG00000231512.6","gene_symbol":"AL606534.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":243029512,"end":243052252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213179.4","gene_symbol":"AC006534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67784753,"end":67785293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071127.16","gene_symbol":"WDR1","gene_name":"WD repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12754]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9948","summary":"This gene encodes a protein containing 9 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, mostly including a trp-asp at the C-terminal end. WD domains are involved in protein-protein interactions. The encoded protein may help induce the disassembly of actin filaments. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":10074339,"end":10116949,"strand":-1,"description":"WD repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:12754]"}, {"versioned_ensembl_gene_id":"ENSG00000164871.17","gene_symbol":"SPAG11B","gene_name":"sperm associated antigen 11B [Source:HGNC Symbol;Acc:HGNC:14534]","synonyms":"EDDM2B,HE2,EP2D,EP2C,EP2","biotype":"protein_coding","ncbi_id":"10407","summary":"This gene encodes several androgen-dependent, epididymis-specific secretory proteins. The specific functions of these proteins have not been determined, but they are thought to be involved in sperm maturation. Some of the isoforms contain regions of similarity to beta-defensins, a family of antimicrobial peptides. The gene is located on chromosome 8p23 near the defensin gene cluster. Alternative splicing of this gene results in seven transcript variants encoding different isoforms. Two different N-terminal and five different C-terminal protein sequences are encoded by the splice variants. Two additional variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]","start":7442684,"end":7463674,"strand":-1,"description":"sperm associated antigen 11B [Source:HGNC Symbol;Acc:HGNC:14534]"}, {"versioned_ensembl_gene_id":"ENSG00000128641.18","gene_symbol":"MYO1B","gene_name":"myosin IB [Source:HGNC Symbol;Acc:HGNC:7596]","synonyms":"myr1","biotype":"protein_coding","ncbi_id":"4430","summary":null,"start":191245185,"end":191425389,"strand":1,"description":"myosin IB [Source:HGNC Symbol;Acc:HGNC:7596]"}, {"versioned_ensembl_gene_id":"ENSG00000128815.19","gene_symbol":"WDFY4","gene_name":"WDFY family member 4 [Source:HGNC Symbol;Acc:HGNC:29323]","synonyms":"Em:AC060234.3,C10orf64,KIAA1607,FLJ45748","biotype":"protein_coding","ncbi_id":"57705","summary":null,"start":48684876,"end":48982956,"strand":1,"description":"WDFY family member 4 [Source:HGNC Symbol;Acc:HGNC:29323]"}, {"versioned_ensembl_gene_id":"ENSG00000072682.18","gene_symbol":"P4HA2","gene_name":"prolyl 4-hydroxylase subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:8547]","synonyms":"C-P4Halpha(II)","biotype":"protein_coding","ncbi_id":"8974","summary":"This gene encodes a component of prolyl 4-hydroxylase, a key enzyme in collagen synthesis composed of two identical alpha subunits and two beta subunits. The encoded protein is one of several different types of alpha subunits and provides the major part of the catalytic site of the active enzyme. In collagen and related proteins, prolyl 4-hydroxylase catalyzes the formation of 4-hydroxyproline that is essential to the proper three-dimensional folding of newly synthesized procollagen chains. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":132191838,"end":132295315,"strand":-1,"description":"prolyl 4-hydroxylase subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:8547]"}, {"versioned_ensembl_gene_id":"ENSG00000266877.1","gene_symbol":"AC007923.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31583162,"end":31637543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264634.1","gene_symbol":"AC100844.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67940949,"end":67956426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166323.12","gene_symbol":"C11orf65","gene_name":"chromosome 11 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:28519]","synonyms":"MGC33948","biotype":"protein_coding","ncbi_id":"160140","summary":null,"start":108308519,"end":108467531,"strand":-1,"description":"chromosome 11 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:28519]"}, {"versioned_ensembl_gene_id":"ENSG00000023171.16","gene_symbol":"GRAMD1B","gene_name":"GRAM domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29214]","synonyms":"LINC01059,KIAA1201","biotype":"protein_coding","ncbi_id":"57476","summary":null,"start":123358428,"end":123627774,"strand":1,"description":"GRAM domain containing 1B [Source:HGNC Symbol;Acc:HGNC:29214]"}, {"versioned_ensembl_gene_id":"ENSG00000248780.1","gene_symbol":"ARL4AP2","gene_name":"ADP ribosylation factor like GTPase 4A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32379]","synonyms":"ARL4P2","biotype":"processed_pseudogene","ncbi_id":"152709","summary":null,"start":40786110,"end":40786710,"strand":1,"description":"ADP ribosylation factor like GTPase 4A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32379]"}, {"versioned_ensembl_gene_id":"ENSG00000108179.13","gene_symbol":"PPIF","gene_name":"peptidylprolyl isomerase F [Source:HGNC Symbol;Acc:HGNC:9259]","synonyms":"hCyP3,Cyp-D","biotype":"protein_coding","ncbi_id":"10105","summary":"The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein is part of the mitochondrial permeability transition pore in the inner mitochondrial membrane. Activation of this pore is thought to be involved in the induction of apoptotic and necrotic cell death. [provided by RefSeq, Jul 2008]","start":79347469,"end":79355337,"strand":1,"description":"peptidylprolyl isomerase F [Source:HGNC Symbol;Acc:HGNC:9259]"}, {"versioned_ensembl_gene_id":"ENSG00000265240.1","gene_symbol":"AC114689.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67830671,"end":67831967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204959.4","gene_symbol":"ARHGEF34P","gene_name":"Rho guanine nucleotide exchange factor 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:38086]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728377","summary":null,"start":144272445,"end":144286966,"strand":-1,"description":"Rho guanine nucleotide exchange factor 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:38086]"}, {"versioned_ensembl_gene_id":"ENSG00000226828.1","gene_symbol":"AL591885.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":243917402,"end":244047317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231864.2","gene_symbol":"AL807752.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137063535,"end":137064581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224015.1","gene_symbol":"AC063976.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132179234,"end":132181128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263594.1","gene_symbol":"AC022655.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67672221,"end":67676078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213214.4","gene_symbol":"ARHGEF35","gene_name":"Rho guanine nucleotide exchange factor 35 [Source:HGNC Symbol;Acc:HGNC:33846]","synonyms":"ARHGEF5L,FLJ43692,CTAGE4","biotype":"protein_coding","ncbi_id":"445328","summary":null,"start":144186083,"end":144195655,"strand":-1,"description":"Rho guanine nucleotide exchange factor 35 [Source:HGNC Symbol;Acc:HGNC:33846]"}, {"versioned_ensembl_gene_id":"ENSG00000214262.4","gene_symbol":"ANKRD36BP1","gene_name":"ankyrin repeat domain 36B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28169]","synonyms":"MGC12538,ANKRD36BL1,ANKRD26L1","biotype":"transcribed_processed_pseudogene","ncbi_id":"84832","summary":null,"start":168245565,"end":168247343,"strand":-1,"description":"ankyrin repeat domain 36B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28169]"}, {"versioned_ensembl_gene_id":"ENSG00000270328.1","gene_symbol":"AC009597.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56776283,"end":56776874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254055.1","gene_symbol":"AC009597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56639901,"end":56656465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172766.18","gene_symbol":"NAA16","gene_name":"N(alpha)-acetyltransferase 16, NatA auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:26164]","synonyms":"PRO2435,NARG1L,MGC40612,FLJ22054","biotype":"protein_coding","ncbi_id":"79612","summary":null,"start":41311205,"end":41377030,"strand":1,"description":"N(alpha)-acetyltransferase 16, NatA auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:26164]"}, {"versioned_ensembl_gene_id":"ENSG00000227616.1","gene_symbol":"AC063976.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":132147491,"end":132149559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233297.4","gene_symbol":"RASA4DP","gene_name":"RAS p21 protein activator 4CD, pseudogene [Source:HGNC Symbol;Acc:HGNC:44226]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100133005","summary":null,"start":102681836,"end":102690469,"strand":-1,"description":"RAS p21 protein activator 4CD, pseudogene [Source:HGNC Symbol;Acc:HGNC:44226]"}, {"versioned_ensembl_gene_id":"ENSG00000154229.11","gene_symbol":"PRKCA","gene_name":"protein kinase C alpha [Source:HGNC Symbol;Acc:HGNC:9393]","synonyms":"PKCA","biotype":"protein_coding","ncbi_id":"5578","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This kinase has been reported to play roles in many different cellular processes, such as cell adhesion, cell transformation, cell cycle checkpoint, and cell volume control. Knockout studies in mice suggest that this kinase may be a fundamental regulator of cardiac contractility and Ca(2+) handling in myocytes. [provided by RefSeq, Jul 2008]","start":66302636,"end":66810743,"strand":1,"description":"protein kinase C alpha [Source:HGNC Symbol;Acc:HGNC:9393]"}, {"versioned_ensembl_gene_id":"ENSG00000141013.16","gene_symbol":"GAS8","gene_name":"growth arrest specific 8 [Source:HGNC Symbol;Acc:HGNC:4166]","synonyms":"GAS11,DRC4","biotype":"protein_coding","ncbi_id":"2622","summary":"This gene includes 11 exons spanning 25 kb and maps to a region of chromosome 16 that is sometimes deleted in breast and prostrate cancer. The second intron contains an apparently intronless gene, C16orf3, that is transcribed in the opposite orientation. This gene is a putative tumor suppressor gene. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":90019629,"end":90044975,"strand":1,"description":"growth arrest specific 8 [Source:HGNC Symbol;Acc:HGNC:4166]"}, {"versioned_ensembl_gene_id":"ENSG00000166923.10","gene_symbol":"GREM1","gene_name":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]","synonyms":"DAND2,CRAC1,CRAC1,CKTSF1B1,HMPS,CKTSF1B1,HMPS,gremlin,gremlin,DRM,DRM,DAND2","biotype":"protein_coding","ncbi_id":"26585","summary":"This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted glycosylated protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to relay the sonic hedgehog (SHH) signal from the polarizing region to the apical ectodermal ridge during limb bud outgrowth. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":32717974,"end":32745107,"strand":1,"description":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]"}, {"versioned_ensembl_gene_id":"ENSG00000278025.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"LY94,CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54977550,"end":54981465,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000244198.5","gene_symbol":"AC004889.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144194858,"end":144280547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279407.1","gene_symbol":"AC007191.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45714387,"end":45717381,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248494.1","gene_symbol":"LNX1-AS2","gene_name":"LNX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41450]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100873955","summary":null,"start":53592956,"end":53604047,"strand":1,"description":"LNX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41450]"}, {"versioned_ensembl_gene_id":"ENSG00000263818.5","gene_symbol":"AC091178.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":39057019,"end":39113190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249341.1","gene_symbol":"AC124017.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53659208,"end":53737156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255483.1","gene_symbol":"AP000889.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107600379,"end":107600868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236495.1","gene_symbol":"AL158168.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14652742,"end":14661691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261490.1","gene_symbol":"AC005674.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":10068089,"end":10073019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188712.4","gene_symbol":"OR13D3P","gene_name":"olfactory receptor family 13 subfamily D member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15106]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402374","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104722335,"end":104723271,"strand":1,"description":"olfactory receptor family 13 subfamily D member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15106]"}, {"versioned_ensembl_gene_id":"ENSG00000255136.2","gene_symbol":"AP001972.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75208054,"end":75241173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231096.1","gene_symbol":"NDUFB4P3","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45251]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288420","summary":null,"start":19840126,"end":19840515,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45251]"}, {"versioned_ensembl_gene_id":"ENSG00000250413.1","gene_symbol":"AC005674.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10006482,"end":10009725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235975.1","gene_symbol":"Z83313.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138806374,"end":138807091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234573.1","gene_symbol":"AL121890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5013520,"end":5013724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132680.10","gene_symbol":"KIAA0907","gene_name":"KIAA0907 [Source:HGNC Symbol;Acc:HGNC:29145]","synonyms":"SNORA80EHG,BLOM7","biotype":"protein_coding","ncbi_id":"22889","summary":null,"start":155913043,"end":155934400,"strand":-1,"description":"KIAA0907 [Source:HGNC Symbol;Acc:HGNC:29145]"}, {"versioned_ensembl_gene_id":"ENSG00000186642.15","gene_symbol":"PDE2A","gene_name":"phosphodiesterase 2A [Source:HGNC Symbol;Acc:HGNC:8777]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5138","summary":null,"start":72576141,"end":72674591,"strand":-1,"description":"phosphodiesterase 2A [Source:HGNC Symbol;Acc:HGNC:8777]"}, {"versioned_ensembl_gene_id":"ENSG00000186446.11","gene_symbol":"ZNF501","gene_name":"zinc finger protein 501 [Source:HGNC Symbol;Acc:HGNC:23717]","synonyms":"ZNF52,MGC21738","biotype":"protein_coding","ncbi_id":"115560","summary":null,"start":44729596,"end":44737083,"strand":1,"description":"zinc finger protein 501 [Source:HGNC Symbol;Acc:HGNC:23717]"}, {"versioned_ensembl_gene_id":"ENSG00000266341.1","gene_symbol":"AC004477.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48060383,"end":48060669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224879.1","gene_symbol":"AC011754.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":79158374,"end":79185523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215765.3","gene_symbol":"AC245128.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276894.1","gene_symbol":"RAB28P4","gene_name":"RAB28, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51548]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132871","summary":null,"start":66641314,"end":66642277,"strand":-1,"description":"RAB28, member RAS oncogene family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51548]"}, {"versioned_ensembl_gene_id":"ENSG00000272134.1","gene_symbol":"AC103810.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64881091,"end":64881181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225920.2","gene_symbol":"RIMKLBP2","gene_name":"ribosomal modification protein rimK like family member B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39163]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422371","summary":null,"start":219199914,"end":219200567,"strand":-1,"description":"ribosomal modification protein rimK like family member B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39163]"}, {"versioned_ensembl_gene_id":"ENSG00000250293.1","gene_symbol":"CRYZP2","gene_name":"crystallin zeta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49203]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526735","summary":null,"start":97916353,"end":97917401,"strand":-1,"description":"crystallin zeta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49203]"}, {"versioned_ensembl_gene_id":"ENSG00000254044.5","gene_symbol":"AC034154.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":97334635,"end":97633823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254846.1","gene_symbol":"AL355075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20344233,"end":20346888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145687.16","gene_symbol":"SSBP2","gene_name":"single stranded DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15831]","synonyms":"HSPC116","biotype":"protein_coding","ncbi_id":"23635","summary":"This gene encodes a subunit of a protein complex that interacts with single-stranded DNA and is involved in the DNA damage response and maintenance of genome stability. The encoded protein may also play a role in telomere repair. A variant of this gene may be associated with survival in human glioblastoma patients. [provided by RefSeq, Sep 2016]","start":81413021,"end":81751797,"strand":-1,"description":"single stranded DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15831]"}, {"versioned_ensembl_gene_id":"ENSG00000237336.1","gene_symbol":"AL445489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123491884,"end":123493156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236991.6","gene_symbol":"EDRF1-AS1","gene_name":"EDRF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49501]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927983","summary":null,"start":125725634,"end":125752110,"strand":-1,"description":"EDRF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49501]"}, {"versioned_ensembl_gene_id":"ENSG00000240979.1","gene_symbol":"AL353813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79726069,"end":79726321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284084.1","gene_symbol":"AC007163.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":200695723,"end":200748040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156502.13","gene_symbol":"SUPV3L1","gene_name":"Suv3 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:11471]","synonyms":"SUV3","biotype":"protein_coding","ncbi_id":"6832","summary":null,"start":69180232,"end":69209099,"strand":1,"description":"Suv3 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:11471]"}, {"versioned_ensembl_gene_id":"ENSG00000186532.11","gene_symbol":"SMYD4","gene_name":"SET and MYND domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21067]","synonyms":"ZMYND21,KIAA1936","biotype":"protein_coding","ncbi_id":"114826","summary":null,"start":1779485,"end":1830634,"strand":-1,"description":"SET and MYND domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21067]"}, {"versioned_ensembl_gene_id":"ENSG00000211876.1","gene_symbol":"TRAJ13","gene_name":"T-cell receptor alpha joining 13 [Source:HGNC Symbol;Acc:HGNC:12041]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28742","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22531076,"end":22531138,"strand":1,"description":"T-cell receptor alpha joining 13 [Source:HGNC Symbol;Acc:HGNC:12041]"}, {"versioned_ensembl_gene_id":"ENSG00000249623.1","gene_symbol":"AC079858.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168647896,"end":168648587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112425.14","gene_symbol":"EPM2A","gene_name":"EPM2A, laforin glucan phosphatase [Source:HGNC Symbol;Acc:HGNC:3413]","synonyms":"LDE,LD","biotype":"protein_coding","ncbi_id":"7957","summary":"This gene encodes a dual-specificity phosphatase and may be involved in the regulation of glycogen metabolism. The protein acts on complex carbohydrates to prevent glycogen hyperphosphorylation, thus avoiding the formation of insoluble aggregates. Loss-of-function mutations in this gene have been associated with Lafora disease, a rare, adult-onset recessive neurodegenerative disease, which results in myoclonus epilepsy and usually results in death several years after the onset of symptoms. The disease is characterized by the accumulation of insoluble particles called Lafora bodies, which are derived from glycogen. [provided by RefSeq, Jan 2018]","start":145382535,"end":145736023,"strand":-1,"description":"EPM2A, laforin glucan phosphatase [Source:HGNC Symbol;Acc:HGNC:3413]"}, {"versioned_ensembl_gene_id":"ENSG00000229226.3","gene_symbol":"BTF3L4P4","gene_name":"basic transcription factor 3 like 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506061","summary":null,"start":168598240,"end":168598757,"strand":-1,"description":"basic transcription factor 3 like 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39648]"}, {"versioned_ensembl_gene_id":"ENSG00000110934.10","gene_symbol":"BIN2","gene_name":"bridging integrator 2 [Source:HGNC Symbol;Acc:HGNC:1053]","synonyms":"BRAP-1","biotype":"protein_coding","ncbi_id":"51411","summary":null,"start":51281038,"end":51324668,"strand":-1,"description":"bridging integrator 2 [Source:HGNC Symbol;Acc:HGNC:1053]"}, {"versioned_ensembl_gene_id":"ENSG00000259000.1","gene_symbol":"DOCK11P1","gene_name":"dedicator of cytokinesis 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31719]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132537","summary":null,"start":44860316,"end":44866247,"strand":-1,"description":"dedicator of cytokinesis 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31719]"}, {"versioned_ensembl_gene_id":"ENSG00000255185.5","gene_symbol":"PDXDC2P","gene_name":"pyridoxal dependent decarboxylase domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:27559]","synonyms":"PDXDC2,DKFZp761H1120","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"109731405","summary":null,"start":70010751,"end":70065945,"strand":-1,"description":"pyridoxal dependent decarboxylase domain containing 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:27559]"}, {"versioned_ensembl_gene_id":"ENSG00000234134.1","gene_symbol":"AL158835.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":125718771,"end":125719365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258487.1","gene_symbol":"LINC02277","gene_name":"long intergenic non-protein coding RNA 2277 [Source:HGNC Symbol;Acc:HGNC:53193]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984027","summary":null,"start":44444747,"end":44480618,"strand":-1,"description":"long intergenic non-protein coding RNA 2277 [Source:HGNC Symbol;Acc:HGNC:53193]"}, {"versioned_ensembl_gene_id":"ENSG00000125741.4","gene_symbol":"OPA3","gene_name":"OPA3, outer mitochondrial membrane lipid metabolism regulator [Source:HGNC Symbol;Acc:HGNC:8142]","synonyms":"MGA3,FLJ22187","biotype":"protein_coding","ncbi_id":"80207","summary":"The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":45527427,"end":45602212,"strand":-1,"description":"OPA3, outer mitochondrial membrane lipid metabolism regulator [Source:HGNC Symbol;Acc:HGNC:8142]"}, {"versioned_ensembl_gene_id":"ENSG00000151006.7","gene_symbol":"PRSS53","gene_name":"protease, serine 53 [Source:HGNC Symbol;Acc:HGNC:34407]","synonyms":"POL3S","biotype":"protein_coding","ncbi_id":"339105","summary":null,"start":31083425,"end":31089628,"strand":-1,"description":"protease, serine 53 [Source:HGNC Symbol;Acc:HGNC:34407]"}, {"versioned_ensembl_gene_id":"ENSG00000254751.2","gene_symbol":"TRIM64DP","gene_name":"tripartite motif containing 64D, pseudogene [Source:HGNC Symbol;Acc:HGNC:43974]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727828","summary":null,"start":89776981,"end":89782377,"strand":1,"description":"tripartite motif containing 64D, pseudogene [Source:HGNC Symbol;Acc:HGNC:43974]"}, {"versioned_ensembl_gene_id":"ENSG00000232598.2","gene_symbol":"AL122034.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36940071,"end":36944675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204456.4","gene_symbol":"AP003122.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89766440,"end":89768836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280189.1","gene_symbol":"AC007614.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49297143,"end":49299762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188101.5","gene_symbol":"ALOX15P2","gene_name":"arachidonate 15-lipoxygenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39027]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642959","summary":null,"start":92913156,"end":92921560,"strand":1,"description":"arachidonate 15-lipoxygenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39027]"}, {"versioned_ensembl_gene_id":"ENSG00000250237.1","gene_symbol":"AC010273.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69038518,"end":69043821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075239.13","gene_symbol":"ACAT1","gene_name":"acetyl-CoA acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:93]","synonyms":"THIL,ACAT","biotype":"protein_coding","ncbi_id":"38","summary":"This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009]","start":108121516,"end":108147776,"strand":1,"description":"acetyl-CoA acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:93]"}, {"versioned_ensembl_gene_id":"ENSG00000196289.7","gene_symbol":"BECN2","gene_name":"beclin 2 [Source:HGNC Symbol;Acc:HGNC:38606]","synonyms":"BECN1P1","biotype":"protein_coding","ncbi_id":"441925","summary":null,"start":241957767,"end":241959062,"strand":1,"description":"beclin 2 [Source:HGNC Symbol;Acc:HGNC:38606]"}, {"versioned_ensembl_gene_id":"ENSG00000258620.1","gene_symbol":"AL135838.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":100406599,"end":100407613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258500.2","gene_symbol":"AL845552.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":100480952,"end":100481274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282529.1","gene_symbol":"TRBV8-2","gene_name":"T-cell receptor beta variable 8-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12245]","synonyms":"TRBV82,TCRBV32S1P","biotype":"TR_V_pseudogene","ncbi_id":"28587","summary":null,"start":142408088,"end":142408357,"strand":1,"description":"T-cell receptor beta variable 8-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12245]"}, {"versioned_ensembl_gene_id":"ENSG00000279955.3","gene_symbol":"AC129778.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65865190,"end":65877274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162244.10","gene_symbol":"RPL29","gene_name":"ribosomal protein L29 [Source:HGNC Symbol;Acc:HGNC:10331]","synonyms":"RPL29P10,L29,HUMRPL29,HIP","biotype":"protein_coding","ncbi_id":"6159","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a cytoplasmic ribosomal protein that is a component of the 60S subunit. The protein belongs to the L29E family of ribosomal proteins. The protein is also a peripheral membrane protein expressed on the cell surface that directly binds heparin. Although this gene was previously reported to map to 3q29-qter, it is believed that it is located at 3p21.3-p21.2. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":51993600,"end":51995942,"strand":-1,"description":"ribosomal protein L29 [Source:HGNC Symbol;Acc:HGNC:10331]"}, {"versioned_ensembl_gene_id":"ENSG00000134851.12","gene_symbol":"TMEM165","gene_name":"transmembrane protein 165 [Source:HGNC Symbol;Acc:HGNC:30760]","synonyms":"TPARL,TMPT27,GDT1","biotype":"protein_coding","ncbi_id":"55858","summary":"This gene encodes a predicted transmembrane protein with a perinuclear Golgi-like distribution in fibroblasts. Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation, type IIk. Knockdown of this gene's expression causes decreased sialylation in HEK cells and suggests this gene plays a role in terminal Golgi glycosylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":55395957,"end":55453397,"strand":1,"description":"transmembrane protein 165 [Source:HGNC Symbol;Acc:HGNC:30760]"}, {"versioned_ensembl_gene_id":"ENSG00000229436.1","gene_symbol":"AC073850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80662331,"end":80662585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166924.8","gene_symbol":"NYAP1","gene_name":"neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 [Source:HGNC Symbol;Acc:HGNC:22009]","synonyms":"KIAA1486L,FLJ37538,C7orf51","biotype":"protein_coding","ncbi_id":"222950","summary":null,"start":100483927,"end":100494799,"strand":1,"description":"neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 [Source:HGNC Symbol;Acc:HGNC:22009]"}, {"versioned_ensembl_gene_id":"ENSG00000211855.1","gene_symbol":"TRAJ34","gene_name":"T-cell receptor alpha joining 34 [Source:HGNC Symbol;Acc:HGNC:12064]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28721","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22507666,"end":22507723,"strand":1,"description":"T-cell receptor alpha joining 34 [Source:HGNC Symbol;Acc:HGNC:12064]"}, {"versioned_ensembl_gene_id":"ENSG00000175749.11","gene_symbol":"EIF3KP1","gene_name":"eukaryotic translation initiation factor 3 subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"134505","summary":null,"start":103032376,"end":103033031,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44016]"}, {"versioned_ensembl_gene_id":"ENSG00000213391.3","gene_symbol":"AF274858.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153606517,"end":153606888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217889.3","gene_symbol":"KRT18P48","gene_name":"keratin 18 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:33418]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340598","summary":null,"start":153604497,"end":153605348,"strand":-1,"description":"keratin 18 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:33418]"}, {"versioned_ensembl_gene_id":"ENSG00000279360.1","gene_symbol":"AC007546.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":110056916,"end":110057275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105997.22","gene_symbol":"HOXA3","gene_name":"homeobox A3 [Source:HGNC Symbol;Acc:HGNC:5104]","synonyms":"HOX1E,HOX1","biotype":"protein_coding","ncbi_id":"3200","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":27106184,"end":27152581,"strand":-1,"description":"homeobox A3 [Source:HGNC Symbol;Acc:HGNC:5104]"}, {"versioned_ensembl_gene_id":"ENSG00000225148.1","gene_symbol":"AL050338.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139856104,"end":139877391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231426.5","gene_symbol":"AL050338.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139854850,"end":139860151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274893.1","gene_symbol":"AL136317.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66014525,"end":66020816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272145.1","gene_symbol":"NFYC-AS1","gene_name":"NFYC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49451]","synonyms":"0808y08y","biotype":"antisense_RNA","ncbi_id":"100130557","summary":null,"start":40690380,"end":40692066,"strand":-1,"description":"NFYC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49451]"}, {"versioned_ensembl_gene_id":"ENSG00000258622.2","gene_symbol":"AL442163.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42657763,"end":42657918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104903.4","gene_symbol":"LYL1","gene_name":"LYL1, basic helix-loop-helix family member [Source:HGNC Symbol;Acc:HGNC:6734]","synonyms":"bHLHa18","biotype":"protein_coding","ncbi_id":"4066","summary":"This gene represents a basic helix-loop-helix transcription factor. The encoded protein may play roles in blood vessel maturation and hematopoeisis. A translocation between this locus and the T cell receptor beta locus (GeneID 6957) on chromosome 7 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Sep 2010]","start":13099033,"end":13103161,"strand":-1,"description":"LYL1, basic helix-loop-helix family member [Source:HGNC Symbol;Acc:HGNC:6734]"}, {"versioned_ensembl_gene_id":"ENSG00000282204.1","gene_symbol":"TRBV9","gene_name":"T-cell receptor beta variable 9 [Source:HGNC Symbol;Acc:HGNC:12246]","synonyms":"TCRBV1S1A1N1,TCRBV9S1","biotype":"TR_V_gene","ncbi_id":"28586","summary":null,"start":142413602,"end":142414123,"strand":1,"description":"T-cell receptor beta variable 9 [Source:HGNC Symbol;Acc:HGNC:12246]"}, {"versioned_ensembl_gene_id":"ENSG00000234355.3","gene_symbol":"FTH1P27","gene_name":"ferritin heavy chain 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39091]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100270709","summary":null,"start":37505310,"end":37505860,"strand":1,"description":"ferritin heavy chain 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39091]"}, {"versioned_ensembl_gene_id":"ENSG00000254702.1","gene_symbol":"AP002353.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107736009,"end":107738718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119408.16","gene_symbol":"NEK6","gene_name":"NIMA related kinase 6 [Source:HGNC Symbol;Acc:HGNC:7749]","synonyms":"SID6-1512","biotype":"protein_coding","ncbi_id":"10783","summary":"The protein encoded by this gene is a kinase required for progression through the metaphase portion of mitosis. Inhibition of the encoded protein can lead to apoptosis. This protein also can enhance tumorigenesis by suppressing tumor cell senescence. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":124257606,"end":124353307,"strand":1,"description":"NIMA related kinase 6 [Source:HGNC Symbol;Acc:HGNC:7749]"}, {"versioned_ensembl_gene_id":"ENSG00000185070.10","gene_symbol":"FLRT2","gene_name":"fibronectin leucine rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:3761]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23768","summary":"This gene encodes a member of the fibronectin leucine rich transmembrane (FLRT) family of cell adhesion molecules, which regulate early embryonic vascular and neural development. The encoded type I transmembrane protein has an extracellular region consisting of an N-terminal leucine-rich repeat domain and a type 3 fibronectin domain, followed by a transmembrane domain and a short C-terminal cytoplasmic tail domain. It functions as both a homophilic cell adhesion molecule and a heterophilic chemorepellent through its interaction with members of the uncoordinated-5 receptor family. Proteolytic removal of the extracellular region controls the migration of neurons in the developing cortex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":85530144,"end":85654426,"strand":1,"description":"fibronectin leucine rich transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:3761]"}, {"versioned_ensembl_gene_id":"ENSG00000113369.8","gene_symbol":"ARRDC3","gene_name":"arrestin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29263]","synonyms":"TLIMP,KIAA1376","biotype":"protein_coding","ncbi_id":"57561","summary":"This gene encodes a member of the arrestin family of proteins, which regulate G protein-mediated signaling. The encoded protein is thought to act as a regulator of breast cancer growth and progression by binding to a phosphorylated form of integrin beta4, a tumor-related antigen, targeting the integrin for internalization and degradation. [provided by RefSeq, Jul 2016]","start":91368724,"end":91383359,"strand":-1,"description":"arrestin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29263]"}, {"versioned_ensembl_gene_id":"ENSG00000231030.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33144520,"end":33145143,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000198663.16","gene_symbol":"C6orf89","gene_name":"chromosome 6 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:21114]","synonyms":"FLJ25357,BRAP","biotype":"protein_coding","ncbi_id":"221477","summary":null,"start":36871870,"end":36928964,"strand":1,"description":"chromosome 6 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:21114]"}, {"versioned_ensembl_gene_id":"ENSG00000276820.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54813971,"end":54828213,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000116171.17","gene_symbol":"SCP2","gene_name":"sterol carrier protein 2 [Source:HGNC Symbol;Acc:HGNC:10606]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6342","summary":"This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms.[provided by RefSeq, Aug 2010]","start":52927229,"end":53051703,"strand":1,"description":"sterol carrier protein 2 [Source:HGNC Symbol;Acc:HGNC:10606]"}, {"versioned_ensembl_gene_id":"ENSG00000275795.1","gene_symbol":"GU182339.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54799171,"end":54811528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231590.1","gene_symbol":"AC235565.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102425428,"end":102428074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130612.14","gene_symbol":"CYP2G1P","gene_name":"cytochrome P450 family 2 subfamily G member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2633]","synonyms":"CYP2GP1,CYP2G1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"22952","summary":null,"start":40890826,"end":40900508,"strand":1,"description":"cytochrome P450 family 2 subfamily G member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2633]"}, {"versioned_ensembl_gene_id":"ENSG00000275732.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54847612,"end":54858688,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000248458.2","gene_symbol":"AL139147.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66665864,"end":66677027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279551.1","gene_symbol":"AC025263.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69660034,"end":69661429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159860.6","gene_symbol":"TCAF2P1","gene_name":"TRPM8 channel associated factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33603]","synonyms":"FLJ40722-like,FAM139B,FAM115D","biotype":"unprocessed_pseudogene","ncbi_id":"653691","summary":null,"start":143800732,"end":143817973,"strand":1,"description":"TRPM8 channel associated factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33603]"}, {"versioned_ensembl_gene_id":"ENSG00000260995.1","gene_symbol":"AL512634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79135422,"end":79145674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267808.1","gene_symbol":"AC018755.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51599289,"end":51600470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240494.2","gene_symbol":"AC005726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28655557,"end":28655983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269388.1","gene_symbol":"AC018755.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":51594561,"end":51606150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112474.4","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"KE6,FABGL,SDR30C1,HKE6,D6S2245E,RING2,H2-KE6","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33133453,"end":33135646,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000135919.12","gene_symbol":"SERPINE2","gene_name":"serpin family E member 2 [Source:HGNC Symbol;Acc:HGNC:8951]","synonyms":"PNI,PN1,PI7,nexin,GDN","biotype":"protein_coding","ncbi_id":"5270","summary":"This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. Thrombin, urokinase, plasmin and trypsin are among the proteases that this family member can inhibit. This gene is a susceptibility gene for chronic obstructive pulmonary disease and for emphysema. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":223975112,"end":224039319,"strand":-1,"description":"serpin family E member 2 [Source:HGNC Symbol;Acc:HGNC:8951]"}, {"versioned_ensembl_gene_id":"ENSG00000136487.17","gene_symbol":"GH2","gene_name":"growth hormone 2 [Source:HGNC Symbol;Acc:HGNC:4262]","synonyms":"hGH-V,GHV,GHL,GH-V","biotype":"protein_coding","ncbi_id":"2689","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. The five genes share a remarkably high degree of sequence identity. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. As in the case of its pituitary counterpart, growth hormone 1, the predominant isoform of this particular family member shows similar somatogenic activity, with reduced lactogenic activity. Mutations in this gene lead to placental growth hormone/lactogen deficiency. [provided by RefSeq, Jul 2008]","start":63880215,"end":63881935,"strand":-1,"description":"growth hormone 2 [Source:HGNC Symbol;Acc:HGNC:4262]"}, {"versioned_ensembl_gene_id":"ENSG00000229671.1","gene_symbol":"LINC01150","gene_name":"long intergenic non-protein coding RNA 1150 [Source:HGNC Symbol;Acc:HGNC:49469]","synonyms":"TCONS_00019134,2G7","biotype":"lincRNA","ncbi_id":"101927624","summary":null,"start":1902647,"end":1907915,"strand":1,"description":"long intergenic non-protein coding RNA 1150 [Source:HGNC Symbol;Acc:HGNC:49469]"}, {"versioned_ensembl_gene_id":"ENSG00000223697.3","gene_symbol":"AF230666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132838117,"end":132844298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248434.1","gene_symbol":"AC107463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135067233,"end":135097658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162894.11","gene_symbol":"FCMR","gene_name":"Fc fragment of IgM receptor [Source:HGNC Symbol;Acc:HGNC:14315]","synonyms":"TOSO,FAIM3","biotype":"protein_coding","ncbi_id":"9214","summary":"Fc receptors specifically bind to the Fc region of immunoglobulins (Igs) to mediate the unique functions of each Ig class. FAIM3 encodes an Fc receptor for IgM (see MIM 147020) (Kubagawa et al., 2009 [PubMed 19858324]; Shima et al., 2010 [PubMed 20042454]).[supplied by OMIM, Jul 2010]","start":206904386,"end":206923247,"strand":-1,"description":"Fc fragment of IgM receptor [Source:HGNC Symbol;Acc:HGNC:14315]"}, {"versioned_ensembl_gene_id":"ENSG00000269371.1","gene_symbol":"AC008878.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7519916,"end":7520460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159164.9","gene_symbol":"SV2A","gene_name":"synaptic vesicle glycoprotein 2A [Source:HGNC Symbol;Acc:HGNC:20566]","synonyms":"SV2,KIAA0736","biotype":"protein_coding","ncbi_id":"9900","summary":"The protein encoded by this gene is one of three related synaptic vesicle proteins. The encoded protein may interact with synaptotagmin to enhance low frequency neurotransmission in quiescent neurons. [provided by RefSeq, Jun 2016]","start":149903318,"end":149917882,"strand":-1,"description":"synaptic vesicle glycoprotein 2A [Source:HGNC Symbol;Acc:HGNC:20566]"}, {"versioned_ensembl_gene_id":"ENSG00000237482.8","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31694505,"end":31695981,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000240280.6","gene_symbol":"TCAM1P","gene_name":"testicular cell adhesion molecule 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:30707]","synonyms":"TCAM1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"146771","summary":"This pseudogene is located downstream from the growth hormone locus on chromosome 17. This locus evolved by a series of partial duplications that have disrupted the human gene. A homologous gene in mouse encodes a testis-specific cell adhesion protein that may play a role in germ cell-Sertoli cell interactions. [provided by RefSeq, Apr 2012]","start":63849292,"end":63864379,"strand":1,"description":"testicular cell adhesion molecule 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:30707]"}, {"versioned_ensembl_gene_id":"ENSG00000228540.1","gene_symbol":"AC073326.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":110724159,"end":110725825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125744.11","gene_symbol":"RTN2","gene_name":"reticulon 2 [Source:HGNC Symbol;Acc:HGNC:10468]","synonyms":"SPG12,NSPL1,NSP2","biotype":"protein_coding","ncbi_id":"6253","summary":"This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. Reticulon proteins also play an important role in the replication of positive-strand RNA (ssRNA) viruses. Mutations at this locus have been associated with autosomal dominant spastic paraplegia-12. [provided by RefSeq, Aug 2020]","start":45485289,"end":45497061,"strand":-1,"description":"reticulon 2 [Source:HGNC Symbol;Acc:HGNC:10468]"}, {"versioned_ensembl_gene_id":"ENSG00000273257.1","gene_symbol":"AC069200.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55387949,"end":55388271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116991.10","gene_symbol":"SIPA1L2","gene_name":"signal induced proliferation associated 1 like 2 [Source:HGNC Symbol;Acc:HGNC:23800]","synonyms":"KIAA1389","biotype":"protein_coding","ncbi_id":"57568","summary":"This gene encodes a member of the signal-induced proliferation-associated 1 like family. Members of this family contain a GTPase activating domain, a PDZ domain and a C-terminal coiled-coil domain with a leucine zipper. A similar protein in rat acts as a GTPases for the small GTPase Rap. [provided by RefSeq, Sep 2015]","start":232397965,"end":232561558,"strand":-1,"description":"signal induced proliferation associated 1 like 2 [Source:HGNC Symbol;Acc:HGNC:23800]"}, {"versioned_ensembl_gene_id":"ENSG00000124212.5","gene_symbol":"PTGIS","gene_name":"prostaglandin I2 synthase [Source:HGNC Symbol;Acc:HGNC:9603]","synonyms":"CYP8A1,PGIS","biotype":"protein_coding","ncbi_id":"5740","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostglandin H2 to prostacyclin (prostaglandin I2), a potent vasodilator and inhibitor of platelet aggregation. An imbalance of prostacyclin and its physiological antagonist thromboxane A2 contribute to the development of myocardial infarction, stroke, and atherosclerosis. [provided by RefSeq, Jul 2008]","start":49503874,"end":49568146,"strand":-1,"description":"prostaglandin I2 synthase [Source:HGNC Symbol;Acc:HGNC:9603]"}, {"versioned_ensembl_gene_id":"ENSG00000229680.4","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587411,"end":29588994,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000182310.13","gene_symbol":"SPACA6","gene_name":"sperm acrosome associated 6 [Source:HGNC Symbol;Acc:HGNC:27113]","synonyms":"SPACA6P,NCRNA00085,LINC00085,LET7EH","biotype":"protein_coding","ncbi_id":"147650","summary":null,"start":51693340,"end":51712387,"strand":1,"description":"sperm acrosome associated 6 [Source:HGNC Symbol;Acc:HGNC:27113]"}, {"versioned_ensembl_gene_id":"ENSG00000235224.1","gene_symbol":"AL591212.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53113018,"end":53113274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179292.4","gene_symbol":"TMEM151A","gene_name":"transmembrane protein 151A [Source:HGNC Symbol;Acc:HGNC:28497]","synonyms":"TMEM151,MGC33486","biotype":"protein_coding","ncbi_id":"256472","summary":null,"start":66291870,"end":66296664,"strand":1,"description":"transmembrane protein 151A [Source:HGNC Symbol;Acc:HGNC:28497]"}, {"versioned_ensembl_gene_id":"ENSG00000109618.11","gene_symbol":"SEPSECS","gene_name":"Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase [Source:HGNC Symbol;Acc:HGNC:30605]","synonyms":"SLA/LP,SLA","biotype":"protein_coding","ncbi_id":"51091","summary":"The amino acid selenocysteine is the only amino acid that does not have its own tRNA synthetase. Instead, this amino acid is synthesized on its cognate tRNA in a three step process. The protein encoded by this gene catalyzes the third step in the process, the conversion of O-phosphoseryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec).[provided by RefSeq, Mar 2011]","start":25120014,"end":25160442,"strand":-1,"description":"Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase [Source:HGNC Symbol;Acc:HGNC:30605]"}, {"versioned_ensembl_gene_id":"ENSG00000138378.17","gene_symbol":"STAT4","gene_name":"signal transducer and activator of transcription 4 [Source:HGNC Symbol;Acc:HGNC:11365]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6775","summary":"The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is essential for mediating responses to IL12 in lymphocytes, and regulating the differentiation of T helper cells. Mutations in this gene may be associated with systemic lupus erythematosus and rheumatoid arthritis. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Aug 2011]","start":191029576,"end":191151596,"strand":-1,"description":"signal transducer and activator of transcription 4 [Source:HGNC Symbol;Acc:HGNC:11365]"}, {"versioned_ensembl_gene_id":"ENSG00000255401.1","gene_symbol":"AC021269.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13488612,"end":13489390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250765.6","gene_symbol":"AC138035.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181329241,"end":181342213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232593.7","gene_symbol":"KANTR","gene_name":"KDM5C adjacent transcript [Source:HGNC Symbol;Acc:HGNC:49510]","synonyms":"Spasm,LINC01155","biotype":"protein_coding","ncbi_id":"102723508","summary":"This gene is thought to produce a functional long non-coding RNA. Mutation of this locus in mouse causes tremors and spastic movements, suggesting a role for this gene in neurological development or function. [provided by RefSeq, Feb 2015]","start":53094145,"end":53170914,"strand":1,"description":"KDM5C adjacent transcript [Source:HGNC Symbol;Acc:HGNC:49510]"}, {"versioned_ensembl_gene_id":"ENSG00000105428.5","gene_symbol":"ZNRF4","gene_name":"zinc and ring finger 4 [Source:HGNC Symbol;Acc:HGNC:17726]","synonyms":"Ssrzf1,spzn,RNF204","biotype":"protein_coding","ncbi_id":"148066","summary":null,"start":5455431,"end":5456856,"strand":1,"description":"zinc and ring finger 4 [Source:HGNC Symbol;Acc:HGNC:17726]"}, {"versioned_ensembl_gene_id":"ENSG00000255330.9","gene_symbol":"SOGA3","gene_name":"SOGA family member 3 [Source:HGNC Symbol;Acc:HGNC:21494]","synonyms":"dJ403A15.3,C6orf174,dJ403A15.3,C6orf174","biotype":"protein_coding","ncbi_id":"387104","summary":null,"start":127438406,"end":127519001,"strand":-1,"description":"SOGA family member 3 [Source:HGNC Symbol;Acc:HGNC:21494]"}, {"versioned_ensembl_gene_id":"ENSG00000241884.2","gene_symbol":"AC114401.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67296300,"end":67306359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274559.3","gene_symbol":"CU639417.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5972924,"end":5973383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231022.1","gene_symbol":"RPS3AP9","gene_name":"ribosomal protein S3a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271129","summary":null,"start":188694320,"end":188695111,"strand":1,"description":"ribosomal protein S3a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36150]"}, {"versioned_ensembl_gene_id":"ENSG00000260343.1","gene_symbol":"LINC01043","gene_name":"long intergenic non-protein coding RNA 1043 [Source:HGNC Symbol;Acc:HGNC:49031]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928752","summary":null,"start":112313467,"end":112321758,"strand":1,"description":"long intergenic non-protein coding RNA 1043 [Source:HGNC Symbol;Acc:HGNC:49031]"}, {"versioned_ensembl_gene_id":"ENSG00000243501.5","gene_symbol":"AL365232.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":73209746,"end":73263196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259168.1","gene_symbol":"AC104002.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27483035,"end":27541991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148288.11","gene_symbol":"GBGT1","gene_name":"globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group) [Source:HGNC Symbol;Acc:HGNC:20460]","synonyms":"UDP-GalNAc,MGC44848,FS,A3GALNT","biotype":"protein_coding","ncbi_id":"26301","summary":"This gene encodes a glycosyltransferase that plays a role in the synthesis of Forssman glycolipid (FG), a member of the globoseries glycolipid family. Glycolipids such as FG form attachment sites for the binding of pathogens to cells; expression of this protein may determine host tropism to microorganisms. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":133152948,"end":133163945,"strand":-1,"description":"globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group) [Source:HGNC Symbol;Acc:HGNC:20460]"}, {"versioned_ensembl_gene_id":"ENSG00000214254.3","gene_symbol":"AC136896.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27208089,"end":27208635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198825.12","gene_symbol":"INPP5F","gene_name":"inositol polyphosphate-5-phosphatase F [Source:HGNC Symbol;Acc:HGNC:17054]","synonyms":"SAC2,KIAA0966,hSac2","biotype":"protein_coding","ncbi_id":"22876","summary":"The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase and contains a Sac domain. The activity of this protein is specific for phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 3,4,5-trisphosphate. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":119726097,"end":119829278,"strand":1,"description":"inositol polyphosphate-5-phosphatase F [Source:HGNC Symbol;Acc:HGNC:17054]"}, {"versioned_ensembl_gene_id":"ENSG00000242729.1","gene_symbol":"AC021006.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41538434,"end":41538986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243150.5","gene_symbol":"AC106707.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158545220,"end":158571066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258836.2","gene_symbol":"AL121579.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58100985,"end":58101574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008988.9","gene_symbol":"RPS20","gene_name":"ribosomal protein S20 [Source:HGNC Symbol;Acc:HGNC:10405]","synonyms":"S20","biotype":"protein_coding","ncbi_id":"6224","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S10P family of ribosomal proteins. It is located in the cytoplasm. This gene is co-transcribed with the small nucleolar RNA gene U54, which is located in its second intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Two transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Apr 2009]","start":56067295,"end":56074581,"strand":-1,"description":"ribosomal protein S20 [Source:HGNC Symbol;Acc:HGNC:10405]"}, {"versioned_ensembl_gene_id":"ENSG00000248275.1","gene_symbol":"TRIM52-AS1","gene_name":"TRIM52 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49006]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507602","summary":null,"start":181261212,"end":181272307,"strand":1,"description":"TRIM52 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49006]"}, {"versioned_ensembl_gene_id":"ENSG00000271368.1","gene_symbol":"AC073387.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109763574,"end":109764357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230192.1","gene_symbol":"AC073387.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109660094,"end":109660802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184368.15","gene_symbol":"MAP7D2","gene_name":"MAP7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25899]","synonyms":"FLJ14503","biotype":"protein_coding","ncbi_id":"256714","summary":null,"start":20006713,"end":20116917,"strand":-1,"description":"MAP7 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25899]"}, {"versioned_ensembl_gene_id":"ENSG00000260892.1","gene_symbol":"AC105020.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75676227,"end":75677162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173546.7","gene_symbol":"CSPG4","gene_name":"chondroitin sulfate proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:2466]","synonyms":"NG2,MSK16,MEL-CSPG,MCSPG,MCSP,HMW-MAA","biotype":"protein_coding","ncbi_id":"1464","summary":"A human melanoma-associated chondroitin sulfate proteoglycan plays a role in stabilizing cell-substratum interactions during early events of melanoma cell spreading on endothelial basement membranes. CSPG4 represents an integral membrane chondroitin sulfate proteoglycan expressed by human malignant melanoma cells. [provided by RefSeq, Jul 2008]","start":75674322,"end":75712848,"strand":-1,"description":"chondroitin sulfate proteoglycan 4 [Source:HGNC Symbol;Acc:HGNC:2466]"}, {"versioned_ensembl_gene_id":"ENSG00000268267.1","gene_symbol":"SIGLEC29P","gene_name":"sialic acid binding Ig like lectin 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:15619]","synonyms":"SIGLECP13","biotype":"unprocessed_pseudogene","ncbi_id":"114188","summary":null,"start":51563797,"end":51564910,"strand":-1,"description":"sialic acid binding Ig like lectin 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:15619]"}, {"versioned_ensembl_gene_id":"ENSG00000282537.1","gene_symbol":"TAS2R43","gene_name":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]","synonyms":"T2R52","biotype":"protein_coding","ncbi_id":"259289","summary":"TAS2R43 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11093151,"end":11094080,"strand":-1,"description":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]"}, {"versioned_ensembl_gene_id":"ENSG00000282546.1","gene_symbol":"AC245078.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11162354,"end":11167587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268257.2","gene_symbol":"AIRN","gene_name":"antisense of IGF2R non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:34515]","synonyms":"NCRNA00088,IGF2RAS,IGF2R-AS1,AIR","biotype":"antisense_RNA","ncbi_id":"100271873","summary":"Both spliced and un-spliced long non-coding RNAs are transcribed from this gene. This gene overlaps on the opposite strand the second intron of the insulin-like growth factor 2 receptor gene; a CpG island associated with the second intron denotes an active promoter that drives the expression of this gene. The related mouse gene is responsible for silencing the insulin-like growth factor 2 receptor gene and flanking genes in the imprinted gene cluster of mice. This gene may be expressed in Wilms tumors. [provided by RefSeq, Feb 2013]","start":160003291,"end":160007664,"strand":-1,"description":"antisense of IGF2R non-protein coding RNA [Source:HGNC Symbol;Acc:HGNC:34515]"}, {"versioned_ensembl_gene_id":"ENSG00000254433.1","gene_symbol":"AP001001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106085990,"end":106101975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262036.1","gene_symbol":"AC068305.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59060029,"end":59061233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255672.1","gene_symbol":"AP002892.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72354516,"end":72363555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268839.1","gene_symbol":"AC020914.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51505059,"end":51505362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250989.1","gene_symbol":"AL390726.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":38543104,"end":38543446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235692.8","gene_symbol":"PFDN6","gene_name":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]","synonyms":"HKE2,H2-KE2,PFD6,KE-2","biotype":"protein_coding","ncbi_id":"10471","summary":"PFDN6 is a subunit of the heteromeric prefoldin complex that chaperones nascent actin (see MIM 102560) and alpha- and beta-tubulin (see MIM 602529 and MIM 191130, respectively) chains pending their transfer to the cytosolic chaperonin containing TCP1 (MIM 186980) (CCT) complex (Hansen et al., 1999 [PubMed 10209023]).[supplied by OMIM, Jul 2010]","start":33459645,"end":33468744,"strand":1,"description":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]"}, {"versioned_ensembl_gene_id":"ENSG00000185567.6","gene_symbol":"AHNAK2","gene_name":"AHNAK nucleoprotein 2 [Source:HGNC Symbol;Acc:HGNC:20125]","synonyms":"C14orf78","biotype":"protein_coding","ncbi_id":"113146","summary":"This gene encodes a large nucleoprotein. The encoded protein has a tripartite domain structure with a relatively short N-terminus and a long C-terminus, separated by a large body of repeats. The N-terminal PSD-95/Discs-large/ZO-1 (PDZ)-like domain is thought to function in the formation of stable homodimers. The encoded protein may play a role in calcium signaling by associating with calcium channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":104937244,"end":104978357,"strand":-1,"description":"AHNAK nucleoprotein 2 [Source:HGNC Symbol;Acc:HGNC:20125]"}, {"versioned_ensembl_gene_id":"ENSG00000131475.6","gene_symbol":"VPS25","gene_name":"vacuolar protein sorting 25 homolog [Source:HGNC Symbol;Acc:HGNC:28122]","synonyms":"MGC10540,EAP20,DERP9","biotype":"protein_coding","ncbi_id":"84313","summary":"This gene encodes a protein that is a subunit of the endosomal sorting complex required for transport II (ESCRT-II). This protein complex functions in sorting of ubiquitinated membrane proteins during endocytosis. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Jul 2013]","start":42773436,"end":42779599,"strand":1,"description":"vacuolar protein sorting 25 homolog [Source:HGNC Symbol;Acc:HGNC:28122]"}, {"versioned_ensembl_gene_id":"ENSG00000249038.2","gene_symbol":"AARSP1","gene_name":"alanyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480683","summary":null,"start":132592084,"end":132592536,"strand":1,"description":"alanyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49894]"}, {"versioned_ensembl_gene_id":"ENSG00000135392.15","gene_symbol":"DNAJC14","gene_name":"DnaJ heat shock protein family (Hsp40) member C14 [Source:HGNC Symbol;Acc:HGNC:24581]","synonyms":"LIP6,HDJ3,FLJ32792,DRIP78,DNAJ","biotype":"protein_coding","ncbi_id":"85406","summary":null,"start":55820960,"end":55830824,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C14 [Source:HGNC Symbol;Acc:HGNC:24581]"}, {"versioned_ensembl_gene_id":"ENSG00000231069.1","gene_symbol":"BX842568.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36985523,"end":36986093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229559.2","gene_symbol":"AL353597.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":37543553,"end":37547280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110025.12","gene_symbol":"SNX15","gene_name":"sorting nexin 15 [Source:HGNC Symbol;Acc:HGNC:14978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29907","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]","start":65027408,"end":65040572,"strand":1,"description":"sorting nexin 15 [Source:HGNC Symbol;Acc:HGNC:14978]"}, {"versioned_ensembl_gene_id":"ENSG00000269181.1","gene_symbol":"AC020914.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51442379,"end":51442650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155052.14","gene_symbol":"CNTNAP5","gene_name":"contactin associated protein like 5 [Source:HGNC Symbol;Acc:HGNC:18748]","synonyms":"FLJ31966,caspr5","biotype":"protein_coding","ncbi_id":"129684","summary":"This gene product belongs to the neurexin family, members of which function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. [provided by RefSeq, Jul 2008]","start":124025287,"end":124915287,"strand":1,"description":"contactin associated protein like 5 [Source:HGNC Symbol;Acc:HGNC:18748]"}, {"versioned_ensembl_gene_id":"ENSG00000128590.4","gene_symbol":"DNAJB9","gene_name":"DnaJ heat shock protein family (Hsp40) member B9 [Source:HGNC Symbol;Acc:HGNC:6968]","synonyms":"MDG1","biotype":"protein_coding","ncbi_id":"4189","summary":"This gene is a member of the J protein family. J proteins function in many cellular processes by regulating the ATPase activity of 70 kDa heat shock proteins. This gene is a member of the type 2 subgroup of DnaJ proteins. The encoded protein is localized to the endoplasmic reticulum. This protein is induced by endoplasmic reticulum stress and plays a role in protecting stressed cells from apoptosis. [provided by RefSeq, Dec 2010]","start":108569568,"end":108574850,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B9 [Source:HGNC Symbol;Acc:HGNC:6968]"}, {"versioned_ensembl_gene_id":"ENSG00000273003.1","gene_symbol":"ARL2-SNX15","gene_name":"ARL2-SNX15 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49197]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528018","summary":"This locus represents naturally occurring read-through transcription between the neighboring ADP-ribosylation factor-like 2 (ARL2) and sorting nexin 15 (SNX15) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":65014182,"end":65040570,"strand":1,"description":"ARL2-SNX15 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49197]"}, {"versioned_ensembl_gene_id":"ENSG00000171540.7","gene_symbol":"OTP","gene_name":"orthopedia homeobox [Source:HGNC Symbol;Acc:HGNC:8518]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23440","summary":"This gene encodes a member of the homeodomain (HD) family. HD family proteins are helix-turn-helix transcription factors that play key roles in the specification of cell fates. This protein may function during brain development. [provided by RefSeq, Jul 2008]","start":77628712,"end":77639688,"strand":-1,"description":"orthopedia homeobox [Source:HGNC Symbol;Acc:HGNC:8518]"}, {"versioned_ensembl_gene_id":"ENSG00000226492.7","gene_symbol":"CUTA","gene_name":"cutA divalent cation tolerance homolog [Source:HGNC Symbol;Acc:HGNC:21101]","synonyms":"C6orf82,ACHAP","biotype":"protein_coding","ncbi_id":"51596","summary":null,"start":33556632,"end":33558507,"strand":-1,"description":"cutA divalent cation tolerance homolog [Source:HGNC Symbol;Acc:HGNC:21101]"}, {"versioned_ensembl_gene_id":"ENSG00000229664.1","gene_symbol":"AL137186.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6025978,"end":6036427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177548.12","gene_symbol":"RABEP2","gene_name":"rabaptin, RAB GTPase binding effector protein 2 [Source:HGNC Symbol;Acc:HGNC:24817]","synonyms":"FLJ23282,FRA","biotype":"protein_coding","ncbi_id":"79874","summary":null,"start":28904421,"end":28936526,"strand":-1,"description":"rabaptin, RAB GTPase binding effector protein 2 [Source:HGNC Symbol;Acc:HGNC:24817]"}, {"versioned_ensembl_gene_id":"ENSG00000229473.2","gene_symbol":"RGS17P1","gene_name":"regulator of G protein signaling 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39729]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128628","summary":null,"start":40992779,"end":40993331,"strand":-1,"description":"regulator of G protein signaling 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39729]"}, {"versioned_ensembl_gene_id":"ENSG00000258675.1","gene_symbol":"LINC02308","gene_name":"long intergenic non-protein coding RNA 2308 [Source:HGNC Symbol;Acc:HGNC:53227]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506700","summary":null,"start":81441987,"end":81450157,"strand":-1,"description":"long intergenic non-protein coding RNA 2308 [Source:HGNC Symbol;Acc:HGNC:53227]"}, {"versioned_ensembl_gene_id":"ENSG00000213724.4","gene_symbol":"PRDX2P2","gene_name":"peroxiredoxin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646218","summary":null,"start":34965069,"end":34966259,"strand":1,"description":"peroxiredoxin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44967]"}, {"versioned_ensembl_gene_id":"ENSG00000224053.1","gene_symbol":"CR788300.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582609,"end":29583126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105426.16","gene_symbol":"PTPRS","gene_name":"protein tyrosine phosphatase, receptor type S [Source:HGNC Symbol;Acc:HGNC:9681]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5802","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular region, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this protein is composed of multiple Ig-like and fibronectin type III-like domains. Studies of the similar gene in mice suggested that this PTP may be involved in cell-cell interaction, primary axonogenesis, and axon guidance during embryogenesis. This PTP has been also implicated in the molecular control of adult nerve repair. Four alternatively spliced transcript variants, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]","start":5158495,"end":5340803,"strand":-1,"description":"protein tyrosine phosphatase, receptor type S [Source:HGNC Symbol;Acc:HGNC:9681]"}, {"versioned_ensembl_gene_id":"ENSG00000215498.9","gene_symbol":"FAM230B","gene_name":"family with sequence similarity 230 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32943]","synonyms":"FLJ46366","biotype":"processed_transcript","ncbi_id":"642633","summary":null,"start":21167758,"end":21192156,"strand":1,"description":"family with sequence similarity 230 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32943]"}, {"versioned_ensembl_gene_id":"ENSG00000230556.1","gene_symbol":"AC073264.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143578907,"end":143579072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225203.2","gene_symbol":"AL139230.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75375511,"end":75377294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264701.1","gene_symbol":"AC018521.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47980398,"end":47996196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248935.1","gene_symbol":"AC034234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60021249,"end":60033020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255012.2","gene_symbol":"OR5M1","gene_name":"olfactory receptor family 5 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8352]","synonyms":"OST050","biotype":"protein_coding","ncbi_id":"390168","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56609236,"end":56614874,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:8352]"}, {"versioned_ensembl_gene_id":"ENSG00000130856.15","gene_symbol":"ZNF236","gene_name":"zinc finger protein 236 [Source:HGNC Symbol;Acc:HGNC:13028]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7776","summary":null,"start":76822607,"end":76970727,"strand":1,"description":"zinc finger protein 236 [Source:HGNC Symbol;Acc:HGNC:13028]"}, {"versioned_ensembl_gene_id":"ENSG00000276214.1","gene_symbol":"AC008833.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59314110,"end":59314800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278085.4","gene_symbol":"CT45A8","gene_name":"cancer/testis antigen family 45 member A8 [Source:HGNC Symbol;Acc:HGNC:51261]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723737","summary":null,"start":135846499,"end":135854538,"strand":-1,"description":"cancer/testis antigen family 45 member A8 [Source:HGNC Symbol;Acc:HGNC:51261]"}, {"versioned_ensembl_gene_id":"ENSG00000268080.2","gene_symbol":"AC016885.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93229659,"end":93229916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250978.5","gene_symbol":"AC079467.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":67463809,"end":67475592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198478.7","gene_symbol":"SH3BGRL2","gene_name":"SH3 domain binding glutamate rich protein like 2 [Source:HGNC Symbol;Acc:HGNC:15567]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83699","summary":null,"start":79631283,"end":79703659,"strand":1,"description":"SH3 domain binding glutamate rich protein like 2 [Source:HGNC Symbol;Acc:HGNC:15567]"}, {"versioned_ensembl_gene_id":"ENSG00000226620.7","gene_symbol":"LINC00343","gene_name":"long intergenic non-protein coding RNA 343 [Source:HGNC Symbol;Acc:HGNC:42500]","synonyms":"NCRNA00344,NCRNA00343,LINC00344","biotype":"processed_transcript","ncbi_id":"144920","summary":null,"start":105704280,"end":105764440,"strand":1,"description":"long intergenic non-protein coding RNA 343 [Source:HGNC Symbol;Acc:HGNC:42500]"}, {"versioned_ensembl_gene_id":"ENSG00000280837.1","gene_symbol":"CPS1-IT1","gene_name":"CPS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:30102]","synonyms":"PRO0132,CPS1IT,CPS1-IT","biotype":"sense_intronic","ncbi_id":"29034","summary":"This gene does not encode a protein, and it is located within an intron of the gene encoding carbamoyl-phosphate synthetase 1. [provided by RefSeq, Jul 2008]","start":210617571,"end":210619876,"strand":1,"description":"CPS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:30102]"}, {"versioned_ensembl_gene_id":"ENSG00000258507.1","gene_symbol":"AC116612.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8858715,"end":8860827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271662.1","gene_symbol":"AC233280.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096006.11","gene_symbol":"CRISP3","gene_name":"cysteine rich secretory protein 3 [Source:HGNC Symbol;Acc:HGNC:16904]","synonyms":"SGP28,dJ442L6.3,CRS3,CRISP-3,Aeg2","biotype":"protein_coding","ncbi_id":"10321","summary":"This gene encodes a member of the cysteine-rich secretory protein (CRISP) family within the CRISP, antigen 5 and pathogenesis-related 1 proteins superfamily. The encoded protein has an N-terminal CRISP, antigen 5 and pathogenesis-related 1 proteins domain, a hinge region, and a C-terminal ion channel regulator domain. This protein contains cysteine residues, located in both the N- and C-terminal domains, that form eight disulfide bonds, a distinguishing characteristic of this family. This gene is expressed in the male reproductive tract where it plays a role in sperm function and fertilization, and the female reproductive tract where it plays a role in endometrial receptivity for embryo implantation. This gene is upregulated in certain types of prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":49727384,"end":49744437,"strand":-1,"description":"cysteine rich secretory protein 3 [Source:HGNC Symbol;Acc:HGNC:16904]"}, {"versioned_ensembl_gene_id":"ENSG00000234834.9","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33041494,"end":33057842,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000171481.4","gene_symbol":"OR1L3","gene_name":"olfactory receptor family 1 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:8215]","synonyms":"OR9-D","biotype":"protein_coding","ncbi_id":"26735","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122675036,"end":122676153,"strand":1,"description":"olfactory receptor family 1 subfamily L member 3 [Source:HGNC Symbol;Acc:HGNC:8215]"}, {"versioned_ensembl_gene_id":"ENSG00000258539.1","gene_symbol":"AC068896.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":124617080,"end":124791727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235597.1","gene_symbol":"LINC01102","gene_name":"long intergenic non-protein coding RNA 1102 [Source:HGNC Symbol;Acc:HGNC:27165]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150568","summary":null,"start":104433267,"end":104520832,"strand":1,"description":"long intergenic non-protein coding RNA 1102 [Source:HGNC Symbol;Acc:HGNC:27165]"}, {"versioned_ensembl_gene_id":"ENSG00000172650.13","gene_symbol":"AGAP5","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 5 [Source:HGNC Symbol;Acc:HGNC:23467]","synonyms":"Em:AC073389.1,CTGLF2","biotype":"protein_coding","ncbi_id":"729092","summary":null,"start":73674285,"end":73698159,"strand":-1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 5 [Source:HGNC Symbol;Acc:HGNC:23467]"}, {"versioned_ensembl_gene_id":"ENSG00000280415.1","gene_symbol":"AC005252.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125858862,"end":125861119,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280125.1","gene_symbol":"AC005252.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":125808668,"end":125809808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144746.6","gene_symbol":"ARL6IP5","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:16937]","synonyms":"Yip6b,PRAF3,JWA,HSPC127,GTRAP3-18,DERP11","biotype":"protein_coding","ncbi_id":"10550","summary":"Expression of this gene is affected by vitamin A. The encoded protein of this gene may be associated with the cytoskeleton. A similar protein in rats may play a role in the regulation of cell differentiation. The rat protein binds and inhibits the cell membrane glutamate transporter EAAC1. The expression of the rat gene is upregulated by retinoic acid, which results in a specific reduction in EAAC1-mediated glutamate transport. [provided by RefSeq, Jul 2008]","start":69084944,"end":69106066,"strand":1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:16937]"}, {"versioned_ensembl_gene_id":"ENSG00000255134.1","gene_symbol":"OR8K2P","gene_name":"olfactory receptor family 8 subfamily K member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14832]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79494","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56335142,"end":56336068,"strand":1,"description":"olfactory receptor family 8 subfamily K member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14832]"}, {"versioned_ensembl_gene_id":"ENSG00000232245.1","gene_symbol":"AL035415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54416256,"end":54420860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140464.19","gene_symbol":"PML","gene_name":"promyelocytic leukemia [Source:HGNC Symbol;Acc:HGNC:9113]","synonyms":"TRIM19,RNF71,MYL","biotype":"protein_coding","ncbi_id":"5371","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This phosphoprotein localizes to nuclear bodies where it functions as a transcription factor and tumor suppressor. Its expression is cell-cycle related and it regulates the p53 response to oncogenic signals. The gene is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL). Extensive alternative splicing of this gene results in several variations of the protein's central and C-terminal regions; all variants encode the same N-terminus. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":73994673,"end":74047812,"strand":1,"description":"promyelocytic leukemia [Source:HGNC Symbol;Acc:HGNC:9113]"}, {"versioned_ensembl_gene_id":"ENSG00000172817.3","gene_symbol":"CYP7B1","gene_name":"cytochrome P450 family 7 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2652]","synonyms":"SPG5A","biotype":"protein_coding","ncbi_id":"9420","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway of extrahepatic tissues, which converts cholesterol to bile acids. This enzyme likely plays a minor role in total bile acid synthesis, but may also be involved in the development of atherosclerosis, neurosteroid metabolism and sex hormone synthesis. Mutations in this gene have been associated with hereditary spastic paraplegia (SPG5 or HSP), an autosomal recessive disorder. [provided by RefSeq, Apr 2016]","start":64587763,"end":64798761,"strand":-1,"description":"cytochrome P450 family 7 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2652]"}, {"versioned_ensembl_gene_id":"ENSG00000271656.1","gene_symbol":"AC007262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81003325,"end":81003645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267458.1","gene_symbol":"AC092069.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12944118,"end":12944487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262801.5","gene_symbol":"U91319.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13246316,"end":13562918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284742.1","gene_symbol":"AL163152.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20183925,"end":20184298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275464.4","gene_symbol":"FP565260.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5130871,"end":5154734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180777.13","gene_symbol":"ANKRD30B","gene_name":"ankyrin repeat domain 30B [Source:HGNC Symbol;Acc:HGNC:24165]","synonyms":"NY-BR-1.1","biotype":"protein_coding","ncbi_id":"374860","summary":null,"start":14728272,"end":14852738,"strand":1,"description":"ankyrin repeat domain 30B [Source:HGNC Symbol;Acc:HGNC:24165]"}, {"versioned_ensembl_gene_id":"ENSG00000261265.1","gene_symbol":"AC025271.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57527187,"end":57529009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265737.1","gene_symbol":"AP006565.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14816151,"end":14825249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185973.10","gene_symbol":"TMLHE","gene_name":"trimethyllysine hydroxylase, epsilon [Source:HGNC Symbol;Acc:HGNC:18308]","synonyms":"XAP130,TMLH,FLJ10727,BBOX2","biotype":"protein_coding","ncbi_id":"55217","summary":"This gene encodes the protein trimethyllysine dioxygenase which is the first enzyme in the carnitine biosynthesis pathway. Carnitine play an essential role in the transport of activated fatty acids across the inner mitochondrial membrane. The encoded protein converts trimethyllysine into hydroxytrimethyllysine. A pseudogene of this gene is found on chromosome X. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":155490115,"end":155669944,"strand":-1,"description":"trimethyllysine hydroxylase, epsilon [Source:HGNC Symbol;Acc:HGNC:18308]"}, {"versioned_ensembl_gene_id":"ENSG00000138463.8","gene_symbol":"DIRC2","gene_name":"disrupted in renal carcinoma 2 [Source:HGNC Symbol;Acc:HGNC:16628]","synonyms":"RCC4,FLJ14784","biotype":"protein_coding","ncbi_id":"84925","summary":"This gene encodes a membrane-bound protein from the major facilitator superfamily of transporters. Disruption of this gene by translocation has been associated with haplo-insufficiency and renal cell carcinomas. Alternatively spliced transcript variants have been described, but their biological validity has not yet been determined. [provided by RefSeq, Jul 2008]","start":122794795,"end":122881139,"strand":1,"description":"disrupted in renal carcinoma 2 [Source:HGNC Symbol;Acc:HGNC:16628]"}, {"versioned_ensembl_gene_id":"ENSG00000213445.9","gene_symbol":"SIPA1","gene_name":"signal-induced proliferation-associated 1 [Source:HGNC Symbol;Acc:HGNC:10885]","synonyms":"SPA1","biotype":"protein_coding","ncbi_id":"6494","summary":"The product of this gene is a mitogen induced GTPase activating protein (GAP). It exhibits a specific GAP activity for Ras-related regulatory proteins Rap1 and Rap2, but not for Ran or other small GTPases. This protein may also hamper mitogen-induced cell cycle progression when abnormally or prematurely expressed. It is localized to the perinuclear region. Two alternatively spliced variants encoding the same isoform have been characterized to date. [provided by RefSeq, Jul 2008]","start":65638097,"end":65650930,"strand":1,"description":"signal-induced proliferation-associated 1 [Source:HGNC Symbol;Acc:HGNC:10885]"}, {"versioned_ensembl_gene_id":"ENSG00000257605.2","gene_symbol":"AC073611.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53298655,"end":53300314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100629.16","gene_symbol":"CEP128","gene_name":"centrosomal protein 128 [Source:HGNC Symbol;Acc:HGNC:20359]","synonyms":"C14orf61,C14orf145","biotype":"protein_coding","ncbi_id":"145508","summary":null,"start":80476983,"end":80959517,"strand":-1,"description":"centrosomal protein 128 [Source:HGNC Symbol;Acc:HGNC:20359]"}, {"versioned_ensembl_gene_id":"ENSG00000232597.5","gene_symbol":"AC013727.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103856659,"end":103880209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267296.2","gene_symbol":"CEBPA-AS1","gene_name":"CEBPA antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:25710]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"80054","summary":null,"start":33302857,"end":33305054,"strand":1,"description":"CEBPA antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:25710]"}, {"versioned_ensembl_gene_id":"ENSG00000184203.7","gene_symbol":"PPP1R2","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 [Source:HGNC Symbol;Acc:HGNC:9288]","synonyms":"IPP2","biotype":"protein_coding","ncbi_id":"5504","summary":"Protein phosphatase-1 (PP1) is one of the main eukaryotic serine/threonine phosphatases. The protein encoded by this gene binds to the catalytic subunit of PP1, strongly inhibiting its activity. Ten related pseudogenes have been found throughout the human genome. Several splice variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":195514425,"end":195543386,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 [Source:HGNC Symbol;Acc:HGNC:9288]"}, {"versioned_ensembl_gene_id":"ENSG00000254876.5","gene_symbol":"AL590705.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":97238449,"end":97297314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186148.13","gene_symbol":"AC013268.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":109933161,"end":109974085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258179.1","gene_symbol":"AC079598.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87820654,"end":87820918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257912.1","gene_symbol":"LINC02258","gene_name":"long intergenic non-protein coding RNA 2258 [Source:HGNC Symbol;Acc:HGNC:53165]","synonyms":"RP11-248E9.5","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87795733,"end":87802028,"strand":1,"description":"long intergenic non-protein coding RNA 2258 [Source:HGNC Symbol;Acc:HGNC:53165]"}, {"versioned_ensembl_gene_id":"ENSG00000260277.1","gene_symbol":"AC009019.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22083256,"end":22092231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239865.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30373944,"end":30391525,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000127663.14","gene_symbol":"KDM4B","gene_name":"lysine demethylase 4B [Source:HGNC Symbol;Acc:HGNC:29136]","synonyms":"TDRD14B,KIAA0876,JMJD2B","biotype":"protein_coding","ncbi_id":"23030","summary":null,"start":4969113,"end":5153595,"strand":1,"description":"lysine demethylase 4B [Source:HGNC Symbol;Acc:HGNC:29136]"}, {"versioned_ensembl_gene_id":"ENSG00000184155.8","gene_symbol":"OR10J5","gene_name":"olfactory receptor family 10 subfamily J member 5 [Source:HGNC Symbol;Acc:HGNC:14993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127385","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159535078,"end":159536007,"strand":-1,"description":"olfactory receptor family 10 subfamily J member 5 [Source:HGNC Symbol;Acc:HGNC:14993]"}, {"versioned_ensembl_gene_id":"ENSG00000257752.1","gene_symbol":"AC091516.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88057876,"end":88058578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254434.1","gene_symbol":"AP006295.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80321620,"end":80327911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279295.1","gene_symbol":"AP001541.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79966805,"end":79968708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255786.1","gene_symbol":"AP000763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73452020,"end":73452344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267786.1","gene_symbol":"AF038458.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35947115,"end":35959192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255209.1","gene_symbol":"AP001978.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79604967,"end":79612300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274015.1","gene_symbol":"AL136038.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63642143,"end":63642696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275532.1","gene_symbol":"AC006449.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38703480,"end":38706261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260272.1","gene_symbol":"AC093525.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2496032,"end":2520218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102239.4","gene_symbol":"BRS3","gene_name":"bombesin receptor subtype 3 [Source:HGNC Symbol;Acc:HGNC:1113]","synonyms":"BB3R,BB3","biotype":"protein_coding","ncbi_id":"680","summary":"The protein encoded by this gene is a G protein-coupled membrane receptor that binds bombesin-like peptides. This binding results in activation of a phosphatidylinositol-calcium second messenger system, with physiological effects including regulation of metabolic rate, glucose metabolism, and hypertension. [provided by RefSeq, Sep 2011]","start":136487887,"end":136493780,"strand":1,"description":"bombesin receptor subtype 3 [Source:HGNC Symbol;Acc:HGNC:1113]"}, {"versioned_ensembl_gene_id":"ENSG00000211460.11","gene_symbol":"TSN","gene_name":"translin [Source:HGNC Symbol;Acc:HGNC:12379]","synonyms":"TRSLN,REHF-1,BCLF-1","biotype":"protein_coding","ncbi_id":"7247","summary":"This gene encodes a DNA-binding protein which specifically recognizes conserved target sequences at the breakpoint junction of chromosomal translocations. Translin polypeptides form a multimeric structure that is responsible for its DNA-binding activity. Recombination-associated motifs and translin-binding sites are present at recombination hotspots and may serve as indicators of breakpoints in genes which are fused by translocations. These binding activities may play a crucial role in chromosomal translocation in lymphoid neoplasms. This protein encoded by this gene, when complexed with translin-associated protein X, also forms a Mg ion-dependent endoribonuclease that promotes RNA-induced silencing complex (RISC) activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":121737103,"end":121767853,"strand":1,"description":"translin [Source:HGNC Symbol;Acc:HGNC:12379]"}, {"versioned_ensembl_gene_id":"ENSG00000270106.5","gene_symbol":"TSNAX-DISC1","gene_name":"TSNAX-DISC1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100303453","summary":"This gene represents naturally occurring read-through transcription between the neighboring TSNAX (translin-associated factor X) and DISC1 (disrupted in schizophrenia 1) genes on chromosome 1. Alternative splicing results in multiple transcript variants, all of which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to be protein-coding. These alterations in gene processing may be associated with risk for psychiatric illness, most notably, schizophrenia. [provided by RefSeq, Nov 2010]","start":231528653,"end":231819244,"strand":1,"description":"TSNAX-DISC1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49177]"}, {"versioned_ensembl_gene_id":"ENSG00000215048.13","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33004965,"end":33016242,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000265631.1","gene_symbol":"AP005901.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15247429,"end":15247997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263883.1","gene_symbol":"EEF1DP7","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51457]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100422656","summary":null,"start":63636601,"end":63637113,"strand":1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51457]"}, {"versioned_ensembl_gene_id":"ENSG00000175938.6","gene_symbol":"ORAI3","gene_name":"ORAI calcium release-activated calcium modulator 3 [Source:HGNC Symbol;Acc:HGNC:28185]","synonyms":"TMEM142C,MGC13024","biotype":"protein_coding","ncbi_id":"93129","summary":null,"start":30949066,"end":30956461,"strand":1,"description":"ORAI calcium release-activated calcium modulator 3 [Source:HGNC Symbol;Acc:HGNC:28185]"}, {"versioned_ensembl_gene_id":"ENSG00000225234.1","gene_symbol":"TRAPPC12-AS1","gene_name":"TRAPPC12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41046]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861515","summary":null,"start":3481242,"end":3482409,"strand":-1,"description":"TRAPPC12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41046]"}, {"versioned_ensembl_gene_id":"ENSG00000261487.1","gene_symbol":"AC135048.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30948386,"end":30956511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260989.1","gene_symbol":"AL133297.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1580527,"end":1610328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234300.1","gene_symbol":"LINC00229","gene_name":"long intergenic non-protein coding RNA 229 [Source:HGNC Symbol;Acc:HGNC:13240]","synonyms":"NCRNA00229,dJ474I12.C22.2,C22orf10","biotype":"lincRNA","ncbi_id":"414351","summary":null,"start":44606939,"end":44625419,"strand":-1,"description":"long intergenic non-protein coding RNA 229 [Source:HGNC Symbol;Acc:HGNC:13240]"}, {"versioned_ensembl_gene_id":"ENSG00000232613.6","gene_symbol":"AC007386.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65030727,"end":65053017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258993.1","gene_symbol":"AL352979.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53023055,"end":53023597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149043.16","gene_symbol":"SYT8","gene_name":"synaptotagmin 8 [Source:HGNC Symbol;Acc:HGNC:19264]","synonyms":"DKFZp434K0322","biotype":"protein_coding","ncbi_id":"90019","summary":"This gene encodes a member of the synaptotagmin protein family. Synaptotagmins are membrane proteins that are important in neurotransmission and hormone secretion, both of which involve regulated exocytosis. Expression of the encoded protein in human pancreatic islets has been connected to activity of the promoter for the insulin gene, on the same chromosome several hundred kilobases away (PMID: 21336277 and 22928559). This association would link response to gluclose to insulin secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":1828307,"end":1837521,"strand":1,"description":"synaptotagmin 8 [Source:HGNC Symbol;Acc:HGNC:19264]"}, {"versioned_ensembl_gene_id":"ENSG00000269907.1","gene_symbol":"AL158827.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96910076,"end":96910405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160318.6","gene_symbol":"CLDND2","gene_name":"claudin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28511]","synonyms":"MGC33839","biotype":"protein_coding","ncbi_id":"125875","summary":null,"start":51367098,"end":51369003,"strand":-1,"description":"claudin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28511]"}, {"versioned_ensembl_gene_id":"ENSG00000224967.1","gene_symbol":"AC009303.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117934025,"end":117934789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282339.1","gene_symbol":"AC010507.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":200499,"end":201174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205029.1","gene_symbol":"OR5D16","gene_name":"olfactory receptor family 5 subfamily D member 16 [Source:HGNC Symbol;Acc:HGNC:15283]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390144","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55838752,"end":55839738,"strand":1,"description":"olfactory receptor family 5 subfamily D member 16 [Source:HGNC Symbol;Acc:HGNC:15283]"}, {"versioned_ensembl_gene_id":"ENSG00000279023.1","gene_symbol":"AC148477.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132360734,"end":132361198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272895.1","gene_symbol":"AC009303.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117998745,"end":117999480,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251482.1","gene_symbol":"AKIRIN2P1","gene_name":"akirin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50796]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216487","summary":null,"start":149789952,"end":149790303,"strand":1,"description":"akirin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50796]"}, {"versioned_ensembl_gene_id":"ENSG00000233450.7","gene_symbol":"KIFC1","gene_name":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]","synonyms":"KNSL2,HSET","biotype":"protein_coding","ncbi_id":"3833","summary":null,"start":33531696,"end":33550087,"strand":1,"description":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]"}, {"versioned_ensembl_gene_id":"ENSG00000277020.4","gene_symbol":"AL590096.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20564708,"end":20567045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282307.1","gene_symbol":"SERPINF1","gene_name":"serpin family F member 1 [Source:HGNC Symbol;Acc:HGNC:8824]","synonyms":"PIG35,PEDF,EPC-1","biotype":"protein_coding","ncbi_id":"5176","summary":"This gene encodes a member of the serpin family that does not display the serine protease inhibitory activity shown by many of the other serpin proteins. The encoded protein is secreted and strongly inhibits angiogenesis. In addition, this protein is a neurotrophic factor involved in neuronal differentiation in retinoblastoma cells. Mutations in this gene were found in individuals with osteogenesis imperfecta, type VI. [provided by RefSeq, Aug 2016]","start":1760880,"end":1765915,"strand":1,"description":"serpin family F member 1 [Source:HGNC Symbol;Acc:HGNC:8824]"}, {"versioned_ensembl_gene_id":"ENSG00000248517.1","gene_symbol":"LINC02437","gene_name":"long intergenic non-protein coding RNA 2437 [Source:HGNC Symbol;Acc:HGNC:53369]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986333","summary":null,"start":184988997,"end":185005186,"strand":1,"description":"long intergenic non-protein coding RNA 2437 [Source:HGNC Symbol;Acc:HGNC:53369]"}, {"versioned_ensembl_gene_id":"ENSG00000236595.1","gene_symbol":"MED15P5","gene_name":"mediator complex subunit 15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391436","summary":null,"start":130251568,"end":130252559,"strand":1,"description":"mediator complex subunit 15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48654]"}, {"versioned_ensembl_gene_id":"ENSG00000141380.13","gene_symbol":"SS18","gene_name":"SS18, nBAF chromatin remodeling complex subunit [Source:HGNC Symbol;Acc:HGNC:11340]","synonyms":"SYT,SSXT","biotype":"protein_coding","ncbi_id":"6760","summary":null,"start":26016253,"end":26091217,"strand":-1,"description":"SS18, nBAF chromatin remodeling complex subunit [Source:HGNC Symbol;Acc:HGNC:11340]"}, {"versioned_ensembl_gene_id":"ENSG00000111057.10","gene_symbol":"KRT18","gene_name":"keratin 18 [Source:HGNC Symbol;Acc:HGNC:6430]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3875","summary":"KRT18 encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. Mutations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":52948871,"end":52952901,"strand":1,"description":"keratin 18 [Source:HGNC Symbol;Acc:HGNC:6430]"}, {"versioned_ensembl_gene_id":"ENSG00000235596.3","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31510228,"end":31511039,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000272223.1","gene_symbol":"AL136304.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43033897,"end":43034405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264458.1","gene_symbol":"AC025211.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32627739,"end":32686484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263717.1","gene_symbol":"AC079336.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32512869,"end":32519350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177335.10","gene_symbol":"C8orf31","gene_name":"chromosome 8 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26731]","synonyms":"FLJ37131","biotype":"processed_transcript","ncbi_id":"286122","summary":null,"start":143039209,"end":143059942,"strand":1,"description":"chromosome 8 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26731]"}, {"versioned_ensembl_gene_id":"ENSG00000282059.1","gene_symbol":"CICP19","gene_name":"capicua transcriptional repressor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:48829]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506706","summary":null,"start":193239,"end":195595,"strand":1,"description":"capicua transcriptional repressor pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:48829]"}, {"versioned_ensembl_gene_id":"ENSG00000175600.15","gene_symbol":"SUGCT","gene_name":"succinyl-CoA:glutarate-CoA transferase [Source:HGNC Symbol;Acc:HGNC:16001]","synonyms":"ORF19,FLJ11808,DERP13,C7orf10","biotype":"protein_coding","ncbi_id":"79783","summary":"This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":40134977,"end":40860763,"strand":1,"description":"succinyl-CoA:glutarate-CoA transferase [Source:HGNC Symbol;Acc:HGNC:16001]"}, {"versioned_ensembl_gene_id":"ENSG00000233820.2","gene_symbol":"AL589843.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":96725890,"end":96727469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274292.1","gene_symbol":"AC084018.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121800797,"end":121803403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261564.1","gene_symbol":"AC120498.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1273751,"end":1276522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269274.1","gene_symbol":"AC078899.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20295089,"end":20303794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280079.1","gene_symbol":"AC011447.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20220597,"end":20222186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135926.14","gene_symbol":"TMBIM1","gene_name":"transmembrane BAX inhibitor motif containing 1 [Source:HGNC Symbol;Acc:HGNC:23410]","synonyms":"RECS1,PP1201,LFG3","biotype":"protein_coding","ncbi_id":"64114","summary":null,"start":218274192,"end":218292586,"strand":-1,"description":"transmembrane BAX inhibitor motif containing 1 [Source:HGNC Symbol;Acc:HGNC:23410]"}, {"versioned_ensembl_gene_id":"ENSG00000130830.14","gene_symbol":"MPP1","gene_name":"membrane palmitoylated protein 1 [Source:HGNC Symbol;Acc:HGNC:7219]","synonyms":"PEMP,DXS552E","biotype":"protein_coding","ncbi_id":"4354","summary":"This gene encodes the prototype of the membrane-associated guanylate kinase (MAGUK) family proteins. MAGUKs interact with the cytoskeleton and regulate cell proliferation, signaling pathways, and intercellular junctions. The encoded protein is an extensively palmitoylated membrane phosphoprotein containing a PDZ domain, a Src homology 3 (SH3) motif, and a guanylate kinase domain. This gene product interacts with various cytoskeletal proteins and cell junctional proteins in different tissue and cell types, and may be involved in the regulation of cell shape, hair cell development, neural patterning of the retina, and apico-basal polarity and tumor suppression pathways in non-erythroid cells. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":154778684,"end":154821007,"strand":-1,"description":"membrane palmitoylated protein 1 [Source:HGNC Symbol;Acc:HGNC:7219]"}, {"versioned_ensembl_gene_id":"ENSG00000106819.11","gene_symbol":"ASPN","gene_name":"asporin [Source:HGNC Symbol;Acc:HGNC:14872]","synonyms":"SLRR1C,PLAP1,FLJ20129","biotype":"protein_coding","ncbi_id":"54829","summary":"This gene encodes a cartilage extracellular protein that is member of the small leucine-rich proteoglycan family. The encoded protein may regulate chondrogenesis by inhibiting transforming growth factor-beta 1-induced gene expression in cartilage. This protein also binds collagen and calcium and may induce collagen mineralization. Polymorphisms in the aspartic acid repeat region of this gene are associated with a susceptibility to osteoarthritis, and also with intervertebral disc disease. Alternative splicing of this gene results in multiple transcript variants.[provided by RefSeq, Jul 2014]","start":92456205,"end":92482506,"strand":-1,"description":"asporin [Source:HGNC Symbol;Acc:HGNC:14872]"}, {"versioned_ensembl_gene_id":"ENSG00000181943.5","gene_symbol":"OR4A21P","gene_name":"olfactory receptor family 4 subfamily A member 21 pseudogene [Source:HGNC Symbol;Acc:HGNC:15158]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81322","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55491205,"end":55492148,"strand":1,"description":"olfactory receptor family 4 subfamily A member 21 pseudogene [Source:HGNC Symbol;Acc:HGNC:15158]"}, {"versioned_ensembl_gene_id":"ENSG00000162888.4","gene_symbol":"C1orf147","gene_name":"chromosome 1 open reading frame 147 [Source:HGNC Symbol;Acc:HGNC:32061]","synonyms":"FLJ32597","biotype":"antisense_RNA","ncbi_id":"574431","summary":null,"start":206491116,"end":206497728,"strand":-1,"description":"chromosome 1 open reading frame 147 [Source:HGNC Symbol;Acc:HGNC:32061]"}, {"versioned_ensembl_gene_id":"ENSG00000233590.1","gene_symbol":"AC016395.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68233251,"end":68242379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069018.17","gene_symbol":"TRPC7","gene_name":"transient receptor potential cation channel subfamily C member 7 [Source:HGNC Symbol;Acc:HGNC:20754]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57113","summary":null,"start":136213320,"end":136365537,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 7 [Source:HGNC Symbol;Acc:HGNC:20754]"}, {"versioned_ensembl_gene_id":"ENSG00000250947.1","gene_symbol":"TRPC7-AS2","gene_name":"TRPC7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40937]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478968","summary":null,"start":136303757,"end":136316100,"strand":1,"description":"TRPC7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40937]"}, {"versioned_ensembl_gene_id":"ENSG00000249675.1","gene_symbol":"AC097487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166388701,"end":166526119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090539.15","gene_symbol":"CHRD","gene_name":"chordin [Source:HGNC Symbol;Acc:HGNC:1949]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8646","summary":"This gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins and sequestering them in latent complexes. The encoded protein may also have roles in organogenesis and during adulthood. It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome. Reduced expression of this gene results in enhanced bone regeneration. Alternative splicing results in multiple transcript variants. Other alternative splice variants have been described but their full length sequence has not been determined. [provided by RefSeq, Jan 2015]","start":184380073,"end":184390736,"strand":1,"description":"chordin [Source:HGNC Symbol;Acc:HGNC:1949]"}, {"versioned_ensembl_gene_id":"ENSG00000173124.14","gene_symbol":"ACSM6","gene_name":"acyl-CoA synthetase medium chain family member 6 [Source:HGNC Symbol;Acc:HGNC:31665]","synonyms":"C10orf129,bA310E22.3","biotype":"protein_coding","ncbi_id":"142827","summary":null,"start":95194200,"end":95228928,"strand":1,"description":"acyl-CoA synthetase medium chain family member 6 [Source:HGNC Symbol;Acc:HGNC:31665]"}, {"versioned_ensembl_gene_id":"ENSG00000275465.5","gene_symbol":"AL449403.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96106661,"end":96116411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105202.8","gene_symbol":"FBL","gene_name":"fibrillarin [Source:HGNC Symbol;Acc:HGNC:3599]","synonyms":"FIB,RNU3IP1,Nop1,FLRN","biotype":"protein_coding","ncbi_id":"2091","summary":"This gene product is a component of a nucleolar small nuclear ribonucleoprotein (snRNP) particle thought to participate in the first step in processing preribosomal RNA. It is associated with the U3, U8, and U13 small nuclear RNAs and is located in the dense fibrillar component (DFC) of the nucleolus. The encoded protein contains an N-terminal repetitive domain that is rich in glycine and arginine residues, like fibrillarins in other species. Its central region resembles an RNA-binding domain and contains an RNP consensus sequence. Antisera from approximately 8% of humans with the autoimmune disease scleroderma recognize fibrillarin. [provided by RefSeq, Jul 2008]","start":39834458,"end":39846414,"strand":-1,"description":"fibrillarin [Source:HGNC Symbol;Acc:HGNC:3599]"}, {"versioned_ensembl_gene_id":"ENSG00000138347.15","gene_symbol":"MYPN","gene_name":"myopalladin [Source:HGNC Symbol;Acc:HGNC:23246]","synonyms":"MYOP","biotype":"protein_coding","ncbi_id":"84665","summary":"Striated muscle in vertebrates comprises large proteins which must be organized properly to contract efficiently. Z-lines in striated muscle are a sign of this organization, representing the ends of actin thin filaments, titin, nebulin or nebulette and accessory proteins required for structure and function. This gene encodes a protein which interacts with nebulin in skeletal muscle or nebulette in cardiac muscle and alpha-actinin. In addition, this gene product can interact with a protein with the I-band indicating it has a regulatory as well as structural function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":68106117,"end":68212017,"strand":1,"description":"myopalladin [Source:HGNC Symbol;Acc:HGNC:23246]"}, {"versioned_ensembl_gene_id":"ENSG00000090565.15","gene_symbol":"RAB11FIP3","gene_name":"RAB11 family interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:17224]","synonyms":"Rab11-FIP3,KIAA0665,eferin","biotype":"protein_coding","ncbi_id":"9727","summary":"Proteins of the large Rab GTPase family (see RAB1A; MIM 179508) have regulatory roles in the formation, targeting, and fusion of intracellular transport vesicles. RAB11FIP3 is one of many proteins that interact with and regulate Rab GTPases (Hales et al., 2001 [PubMed 11495908]).[supplied by OMIM, Mar 2008]","start":425619,"end":523011,"strand":1,"description":"RAB11 family interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:17224]"}, {"versioned_ensembl_gene_id":"ENSG00000280446.1","gene_symbol":"AL607033.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131831910,"end":131833508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236846.1","gene_symbol":"AL359979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":223144049,"end":223144954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226601.1","gene_symbol":"AL359979.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":223181144,"end":223188154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168995.13","gene_symbol":"SIGLEC7","gene_name":"sialic acid binding Ig like lectin 7 [Source:HGNC Symbol;Acc:HGNC:10876]","synonyms":"SIGLECP2,SIGLEC19P,SIGLEC-7,QA79,p75/AIRM1,CD328","biotype":"protein_coding","ncbi_id":"27036","summary":null,"start":51142299,"end":51153526,"strand":1,"description":"sialic acid binding Ig like lectin 7 [Source:HGNC Symbol;Acc:HGNC:10876]"}, {"versioned_ensembl_gene_id":"ENSG00000241388.4","gene_symbol":"HNF1A-AS1","gene_name":"HNF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26785]","synonyms":"FLJ38690,C12orf27,NCRNA00262","biotype":"processed_transcript","ncbi_id":"283460","summary":null,"start":120941728,"end":120980965,"strand":-1,"description":"HNF1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26785]"}, {"versioned_ensembl_gene_id":"ENSG00000182376.2","gene_symbol":"AC138028.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88742767,"end":88745748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197744.5","gene_symbol":"PTMAP2","gene_name":"prothymosin, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5759","summary":null,"start":118973796,"end":118974122,"strand":1,"description":"prothymosin, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9625]"}, {"versioned_ensembl_gene_id":"ENSG00000138964.16","gene_symbol":"PARVG","gene_name":"parvin gamma [Source:HGNC Symbol;Acc:HGNC:14654]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64098","summary":"Members of the parvin family, including PARVG, are actin-binding proteins associated with focal contacts.[supplied by OMIM, Aug 2004]","start":44172956,"end":44219533,"strand":1,"description":"parvin gamma [Source:HGNC Symbol;Acc:HGNC:14654]"}, {"versioned_ensembl_gene_id":"ENSG00000227780.5","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"fru,ZNF297,BING1,ZBTB22A,fruitless,ZNF297A","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33292340,"end":33295864,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000175538.10","gene_symbol":"KCNE3","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:6243]","synonyms":"MiRP2,HOKPP","biotype":"protein_coding","ncbi_id":"10008","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the kidney. A missense mutation in this gene is associated with hypokalemic periodic paralysis. [provided by RefSeq, Jul 2008]","start":74454841,"end":74467729,"strand":-1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 3 [Source:HGNC Symbol;Acc:HGNC:6243]"}, {"versioned_ensembl_gene_id":"ENSG00000277956.4","gene_symbol":"MAPT","gene_name":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]","synonyms":"PPP1R103,MAPTL,PPND,FTDP-17,MTBT2,FLJ31424,MTBT1,DDPAC,MSTD,tau,MGC138549","biotype":"protein_coding","ncbi_id":"4137","summary":"This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008]","start":45906010,"end":46039943,"strand":1,"description":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]"}, {"versioned_ensembl_gene_id":"ENSG00000169612.3","gene_symbol":"FAM103A1","gene_name":"family with sequence similarity 103 member A1 [Source:HGNC Symbol;Acc:HGNC:31022]","synonyms":"HsT19360,C15orf18,RAM,MGC2560","biotype":"protein_coding","ncbi_id":"83640","summary":null,"start":82986207,"end":82991057,"strand":1,"description":"family with sequence similarity 103 member A1 [Source:HGNC Symbol;Acc:HGNC:31022]"}, {"versioned_ensembl_gene_id":"ENSG00000255493.2","gene_symbol":"AP005639.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55430478,"end":55432370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150938.9","gene_symbol":"CRIM1","gene_name":"cysteine rich transmembrane BMP regulator 1 [Source:HGNC Symbol;Acc:HGNC:2359]","synonyms":"S52","biotype":"protein_coding","ncbi_id":"51232","summary":"This gene encodes a transmembrane protein containing six cysteine-rich repeat domains and an insulin-like growth factor-binding domain. The encoded protein may play a role in tissue development though interactions with members of the transforming growth factor beta family, such as bone morphogenetic proteins. [provided by RefSeq, Nov 2010]","start":36355926,"end":36551135,"strand":1,"description":"cysteine rich transmembrane BMP regulator 1 [Source:HGNC Symbol;Acc:HGNC:2359]"}, {"versioned_ensembl_gene_id":"ENSG00000004799.7","gene_symbol":"PDK4","gene_name":"pyruvate dehydrogenase kinase 4 [Source:HGNC Symbol;Acc:HGNC:8812]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5166","summary":"This gene is a member of the PDK/BCKDK protein kinase family and encodes a mitochondrial protein with a histidine kinase domain. This protein is located in the matrix of the mitrochondria and inhibits the pyruvate dehydrogenase complex by phosphorylating one of its subunits, thereby contributing to the regulation of glucose metabolism. Expression of this gene is regulated by glucocorticoids, retinoic acid and insulin. [provided by RefSeq, Jul 2008]","start":95583499,"end":95596491,"strand":-1,"description":"pyruvate dehydrogenase kinase 4 [Source:HGNC Symbol;Acc:HGNC:8812]"}, {"versioned_ensembl_gene_id":"ENSG00000267756.1","gene_symbol":"AC006557.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14074912,"end":14075741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213239.3","gene_symbol":"NPM1P32","gene_name":"nucleophosmin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:45211]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440902","summary":null,"start":121708512,"end":121709115,"strand":-1,"description":"nucleophosmin 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:45211]"}, {"versioned_ensembl_gene_id":"ENSG00000253948.1","gene_symbol":"AC104986.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98996763,"end":99013044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254723.1","gene_symbol":"OR4A12P","gene_name":"olfactory receptor family 4 subfamily A member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15149]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81331","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55325756,"end":55326673,"strand":1,"description":"olfactory receptor family 4 subfamily A member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15149]"}, {"versioned_ensembl_gene_id":"ENSG00000114405.10","gene_symbol":"C3orf14","gene_name":"chromosome 3 open reading frame 14 [Source:HGNC Symbol;Acc:HGNC:25024]","synonyms":"HT021","biotype":"protein_coding","ncbi_id":"57415","summary":null,"start":62318973,"end":62336213,"strand":1,"description":"chromosome 3 open reading frame 14 [Source:HGNC Symbol;Acc:HGNC:25024]"}, {"versioned_ensembl_gene_id":"ENSG00000135597.18","gene_symbol":"REPS1","gene_name":"RALBP1 associated Eps domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15578]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85021","summary":"This gene encodes a signaling adaptor protein with two EH domains that interacts with proteins that participate in signaling, endocytosis and cytoskeletal changes. The encoded protein has been found in association with intersectin 1 and Src homology 3-domain growth factor receptor-bound 2-like (endophilin) interacting protein 1 when intersectin 1 was isolated from clathrin-coated pits. The encoded protein has also been shown to interact with amphiphysin, a cytoplasmic protein at the surface of synaptic vesicles. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":138903493,"end":138988261,"strand":-1,"description":"RALBP1 associated Eps domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15578]"}, {"versioned_ensembl_gene_id":"ENSG00000129450.8","gene_symbol":"SIGLEC9","gene_name":"sialic acid binding Ig like lectin 9 [Source:HGNC Symbol;Acc:HGNC:10878]","synonyms":"CD329","biotype":"protein_coding","ncbi_id":"27180","summary":null,"start":51124908,"end":51136651,"strand":1,"description":"sialic acid binding Ig like lectin 9 [Source:HGNC Symbol;Acc:HGNC:10878]"}, {"versioned_ensembl_gene_id":"ENSG00000244676.5","gene_symbol":"AL109761.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17793488,"end":17810845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261812.6","gene_symbol":"TUBB8P7","gene_name":"tubulin beta 8 class VIII pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42345]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"197331","summary":null,"start":90093154,"end":90096354,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42345]"}, {"versioned_ensembl_gene_id":"ENSG00000126856.13","gene_symbol":"PRDM7","gene_name":"PR/SET domain 7 [Source:HGNC Symbol;Acc:HGNC:9351]","synonyms":"ZNF910","biotype":"protein_coding","ncbi_id":"11105","summary":"This gene encodes a member of a family of proteins that may have roles in transcription and other nuclear processes. The encoded protein contains a KRAB (Kruppel-associated box) domain -A box and a SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain and may function as a histone methyltransferase. [provided by RefSeq, Aug 2013]","start":90056566,"end":90092072,"strand":-1,"description":"PR/SET domain 7 [Source:HGNC Symbol;Acc:HGNC:9351]"}, {"versioned_ensembl_gene_id":"ENSG00000170477.12","gene_symbol":"KRT4","gene_name":"keratin 4 [Source:HGNC Symbol;Acc:HGNC:6441]","synonyms":"K4,CYK4,CK4","biotype":"protein_coding","ncbi_id":"3851","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in differentiated layers of the mucosal and esophageal epithelia with family member KRT13. Mutations in these genes have been associated with White Sponge Nevus, characterized by oral, esophageal, and anal leukoplakia. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52806549,"end":52814551,"strand":-1,"description":"keratin 4 [Source:HGNC Symbol;Acc:HGNC:6441]"}, {"versioned_ensembl_gene_id":"ENSG00000256312.1","gene_symbol":"AC138466.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132190213,"end":132190997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226994.7","gene_symbol":"AC012593.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34799850,"end":35185689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271480.1","gene_symbol":"MTND3P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075161","summary":null,"start":100050719,"end":100051063,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52081]"}, {"versioned_ensembl_gene_id":"ENSG00000255110.1","gene_symbol":"AP005597.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55279949,"end":55280289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256576.2","gene_symbol":"LINC02361","gene_name":"long intergenic non-protein coding RNA 2361 [Source:HGNC Symbol;Acc:HGNC:53283]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996246","summary":null,"start":132186735,"end":132189695,"strand":-1,"description":"long intergenic non-protein coding RNA 2361 [Source:HGNC Symbol;Acc:HGNC:53283]"}, {"versioned_ensembl_gene_id":"ENSG00000271257.1","gene_symbol":"AC008814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58503295,"end":58503700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133597.10","gene_symbol":"ADCK2","gene_name":"aarF domain containing kinase 2 [Source:HGNC Symbol;Acc:HGNC:19039]","synonyms":"MGC20727","biotype":"protein_coding","ncbi_id":"90956","summary":null,"start":140673153,"end":140696261,"strand":1,"description":"aarF domain containing kinase 2 [Source:HGNC Symbol;Acc:HGNC:19039]"}, {"versioned_ensembl_gene_id":"ENSG00000205922.4","gene_symbol":"ONECUT3","gene_name":"one cut homeobox 3 [Source:HGNC Symbol;Acc:HGNC:13399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390874","summary":null,"start":1752373,"end":1780988,"strand":1,"description":"one cut homeobox 3 [Source:HGNC Symbol;Acc:HGNC:13399]"}, {"versioned_ensembl_gene_id":"ENSG00000178449.8","gene_symbol":"COX14","gene_name":"COX14, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:28216]","synonyms":"MGC14288,C12orf62","biotype":"protein_coding","ncbi_id":"84987","summary":"This gene encodes a small single-pass transmembrane protein that localizes to mitochondria. This protein may play a role in coordinating the early steps of cytochrome c oxidase (COX; also known as complex IV) subunit assembly and, in particular, the synthesis and assembly of the COX I subunit of the holoenzyme. Mutations in this gene have been associated with mitochondrial complex IV deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":50111979,"end":50120457,"strand":1,"description":"COX14, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:28216]"}, {"versioned_ensembl_gene_id":"ENSG00000136169.16","gene_symbol":"SETDB2","gene_name":"SET domain bifurcated 2 [Source:HGNC Symbol;Acc:HGNC:20263]","synonyms":"KMT1F,CLLL8,CLLD8,C13orf4","biotype":"protein_coding","ncbi_id":"83852","summary":"This gene encodes a member of a family of proteins that contain a methyl-CpG-binding domain (MBD) and a SET domain and function as histone methyltransferases. This protein is recruited to heterochromatin and plays a role in the regulation of chromosome segregation. This region is commonly deleted in chronic lymphocytic leukemia. Naturally-occuring readthrough transcription occurs from this gene to the downstream PHF11 (PHD finger protein 11) gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":49444374,"end":49495003,"strand":1,"description":"SET domain bifurcated 2 [Source:HGNC Symbol;Acc:HGNC:20263]"}, {"versioned_ensembl_gene_id":"ENSG00000259776.1","gene_symbol":"AC093426.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239247808,"end":239250818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205177.6","gene_symbol":"C11orf91","gene_name":"chromosome 11 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:34444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131378","summary":null,"start":33698261,"end":33700801,"strand":-1,"description":"chromosome 11 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:34444]"}, {"versioned_ensembl_gene_id":"ENSG00000282799.1","gene_symbol":"KANSL1-AS1","gene_name":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644246","summary":null,"start":46205177,"end":46208324,"strand":1,"description":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]"}, {"versioned_ensembl_gene_id":"ENSG00000255391.1","gene_symbol":"AP003497.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87480736,"end":87481297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265717.1","gene_symbol":"AC103808.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76254292,"end":76255214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272172.1","gene_symbol":"AC138696.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143290399,"end":143290621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231829.2","gene_symbol":"AL157834.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95141925,"end":95168425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093009.9","gene_symbol":"CDC45","gene_name":"cell division cycle 45 [Source:HGNC Symbol;Acc:HGNC:1739]","synonyms":"CDC45L2,CDC45L","biotype":"protein_coding","ncbi_id":"8318","summary":"The protein encoded by this gene was identified by its strong similarity with Saccharomyces cerevisiae Cdc45, an essential protein required to the initiation of DNA replication. Cdc45 is a member of the highly conserved multiprotein complex including Cdc6/Cdc18, the minichromosome maintenance proteins (MCMs) and DNA polymerase, which is important for early steps of DNA replication in eukaryotes. This protein has been shown to interact with MCM7 and DNA polymerase alpha. Studies of the similar gene in Xenopus suggested that this protein play a pivotal role in the loading of DNA polymerase alpha onto chromatin. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":19479459,"end":19520612,"strand":1,"description":"cell division cycle 45 [Source:HGNC Symbol;Acc:HGNC:1739]"}, {"versioned_ensembl_gene_id":"ENSG00000223629.1","gene_symbol":"DEFA8P","gene_name":"defensin alpha 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:31799]","synonyms":"DEFAP1","biotype":"unprocessed_pseudogene","ncbi_id":"449491","summary":null,"start":6950726,"end":6951599,"strand":-1,"description":"defensin alpha 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:31799]"}, {"versioned_ensembl_gene_id":"ENSG00000231172.2","gene_symbol":"AC007099.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75524068,"end":75542706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255320.1","gene_symbol":"AP000759.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66244840,"end":66246239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225620.1","gene_symbol":"AC104463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":202632428,"end":202632911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121454.5","gene_symbol":"LHX4","gene_name":"LIM homeobox 4 [Source:HGNC Symbol;Acc:HGNC:21734]","synonyms":"Gsh4","biotype":"protein_coding","ncbi_id":"89884","summary":"This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor involved in the control of differentiation and development of the pituitary gland. Mutations in this gene cause combined pituitary hormone deficiency 4. [provided by RefSeq, Dec 2010]","start":180230286,"end":180278982,"strand":1,"description":"LIM homeobox 4 [Source:HGNC Symbol;Acc:HGNC:21734]"}, {"versioned_ensembl_gene_id":"ENSG00000250603.1","gene_symbol":"AC068658.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127838486,"end":127857804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225275.4","gene_symbol":"NUP210P2","gene_name":"nucleoporin 210 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42707]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129929","summary":null,"start":11900011,"end":11901245,"strand":1,"description":"nucleoporin 210 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42707]"}, {"versioned_ensembl_gene_id":"ENSG00000228383.6","gene_symbol":"FAM197Y7","gene_name":"family with sequence similarity 197 Y-linked member 7 [Source:HGNC Symbol;Acc:HGNC:37469]","synonyms":"FAM197Y7P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"105379269","summary":null,"start":9367803,"end":9377092,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 7 [Source:HGNC Symbol;Acc:HGNC:37469]"}, {"versioned_ensembl_gene_id":"ENSG00000138802.11","gene_symbol":"SEC24B","gene_name":"SEC24 homolog B, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10704]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10427","summary":"The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein is thought to be a cargo-binding component of the COPII vesicle, and is thought to be involved in the transport of secretory proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in this gene have been associated with neural tube defects, and are thought to be a result of a disruption in interactions with the protein encoded by the VANGL planar cell polarity protein 2 (VANGL2) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":109433772,"end":109540896,"strand":1,"description":"SEC24 homolog B, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10704]"}, {"versioned_ensembl_gene_id":"ENSG00000244183.1","gene_symbol":"AC104164.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60732144,"end":60732636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240097.1","gene_symbol":"AC104164.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60616822,"end":60618079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253834.1","gene_symbol":"AC025524.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61821481,"end":61825252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101928.12","gene_symbol":"MOSPD1","gene_name":"motile sperm domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25235]","synonyms":"dJ473B4","biotype":"protein_coding","ncbi_id":"56180","summary":null,"start":134887626,"end":134915267,"strand":-1,"description":"motile sperm domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25235]"}, {"versioned_ensembl_gene_id":"ENSG00000172717.15","gene_symbol":"FAM71D","gene_name":"family with sequence similarity 71 member D [Source:HGNC Symbol;Acc:HGNC:20101]","synonyms":"C14orf54","biotype":"protein_coding","ncbi_id":"161142","summary":null,"start":67189393,"end":67228550,"strand":1,"description":"family with sequence similarity 71 member D [Source:HGNC Symbol;Acc:HGNC:20101]"}, {"versioned_ensembl_gene_id":"ENSG00000138279.15","gene_symbol":"ANXA7","gene_name":"annexin A7 [Source:HGNC Symbol;Acc:HGNC:545]","synonyms":"ANX7","biotype":"protein_coding","ncbi_id":"310","summary":"Annexin VII is a member of the annexin family of calcium-dependent phospholipid binding proteins.The Annexin VII gene contains 14 exons and spans approximately 34 kb of DNA. An alternatively spliced cassette exon results in two mRNA transcripts of 2.0 and 2.4 kb which are predicted to generate two protein isoforms differing in their N-terminal domain. The alternative splicing event is tissue specific and the mRNA containing the cassette exon is prevalent in brain, heart and skeletal muscle. The transcripts also differ in their 3'-non coding regions by the use of two alternative poly(A) signals. Annexin VII encodes a protein with a molecular weight of approximately 51 kDa with a unique, highly hydrophobic N-terminal domain of 167 amino acids and a conserved C-terminal region of 299 amino acids. The latter domain is composed of alternating hydrophobic and hydrophilic segments. Structural analysis of the protein suggests that Annexin VII is a membrane binding protein with diverse properties, including voltage-sensitive calcium channel activity, ion selectivity and membrane fusion. [provided by RefSeq, Jul 2008]","start":73375101,"end":73414076,"strand":-1,"description":"annexin A7 [Source:HGNC Symbol;Acc:HGNC:545]"}, {"versioned_ensembl_gene_id":"ENSG00000272967.1","gene_symbol":"AC073352.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119579212,"end":119579650,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168795.4","gene_symbol":"ZBTB5","gene_name":"zinc finger and BTB domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23836]","synonyms":"KIAA0354","biotype":"protein_coding","ncbi_id":"9925","summary":null,"start":37438114,"end":37465399,"strand":-1,"description":"zinc finger and BTB domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23836]"}, {"versioned_ensembl_gene_id":"ENSG00000240320.1","gene_symbol":"RPS29P27","gene_name":"ribosomal protein S29 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:35836]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271592","summary":null,"start":39697904,"end":39698073,"strand":1,"description":"ribosomal protein S29 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:35836]"}, {"versioned_ensembl_gene_id":"ENSG00000283174.1","gene_symbol":"AL590396.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":237940762,"end":237941061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243781.1","gene_symbol":"AL590396.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":237926831,"end":237927605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229253.5","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"ZNF297,BING1,ZBTB22A,fruitless,ZNF297A,fru","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33236020,"end":33239546,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000280068.1","gene_symbol":"AC138965.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":175903874,"end":175904371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146143.17","gene_symbol":"PRIM2","gene_name":"primase (DNA) subunit 2 [Source:HGNC Symbol;Acc:HGNC:9370]","synonyms":"PRIM2A","biotype":"protein_coding","ncbi_id":"5558","summary":"This gene encodes the 58 kilodalton subunit of DNA primase, an enzyme that plays a key role in the replication of DNA. The encoded protein forms a heterodimer with a 49 kilodalton subunit. This heterodimer functions as a DNA-directed RNA polymerase to synthesize small RNA primers that are used to create Okazaki fragments on the lagging strand of the DNA. Alternative splicing of this gene results in multiple transcript variants. This gene has a related pseudogene, which is also present on chromosome 6. [provided by RefSeq, Apr 2014]","start":57314805,"end":57646849,"strand":1,"description":"primase (DNA) subunit 2 [Source:HGNC Symbol;Acc:HGNC:9370]"}, {"versioned_ensembl_gene_id":"ENSG00000255155.1","gene_symbol":"AP004371.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130544643,"end":130544856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236635.2","gene_symbol":"LINC02540","gene_name":"long intergenic non-protein coding RNA 2540 [Source:HGNC Symbol;Acc:HGNC:53573]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377860","summary":null,"start":76522451,"end":76593623,"strand":-1,"description":"long intergenic non-protein coding RNA 2540 [Source:HGNC Symbol;Acc:HGNC:53573]"}, {"versioned_ensembl_gene_id":"ENSG00000271781.1","gene_symbol":"AC026740.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":675826,"end":676616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113360.16","gene_symbol":"DROSHA","gene_name":"drosha ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17904]","synonyms":"RNASE3L,RN3,HSA242976,Etohi2,RNASEN","biotype":"protein_coding","ncbi_id":"29102","summary":"This gene encodes a ribonuclease (RNase) III double-stranded RNA-specific ribonuclease and subunit of the microprocessor protein complex, which catalyzes the initial processing step of microRNA (miRNA) synthesis. The encoded protein cleaves the stem loop structure from the primary microRNA (pri-miRNA) in the nucleus, yielding the precursor miRNA (pre-miRNA), which is then exported to the cytoplasm for further processing. In a human cell line lacking a functional copy of this gene, canonical miRNA synthesis is reduced. Somatic mutations in this gene have been observed in human patients with kidney cancer. [provided by RefSeq, Sep 2016]","start":31400497,"end":31532196,"strand":-1,"description":"drosha ribonuclease III [Source:HGNC Symbol;Acc:HGNC:17904]"}, {"versioned_ensembl_gene_id":"ENSG00000164244.20","gene_symbol":"PRRC1","gene_name":"proline rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28164]","synonyms":"FLJ32875","biotype":"protein_coding","ncbi_id":"133619","summary":null,"start":127517609,"end":127555089,"strand":1,"description":"proline rich coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:28164]"}, {"versioned_ensembl_gene_id":"ENSG00000203472.3","gene_symbol":"AC009163.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75475896,"end":75495407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183196.8","gene_symbol":"CHST6","gene_name":"carbohydrate sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:6938]","synonyms":"MCDC1","biotype":"protein_coding","ncbi_id":"4166","summary":"The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD). [provided by RefSeq, Jan 2010]","start":75472052,"end":75495384,"strand":-1,"description":"carbohydrate sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:6938]"}, {"versioned_ensembl_gene_id":"ENSG00000153294.11","gene_symbol":"ADGRF4","gene_name":"adhesion G protein-coupled receptor F4 [Source:HGNC Symbol;Acc:HGNC:19011]","synonyms":"PGR18,GPR115,FLJ38076","biotype":"protein_coding","ncbi_id":"221393","summary":"Sequence analysis of this gene suggests that it is encodes a member of the superfamily of G protein-couple receptors. G protein-coupled receptors typically contain seven hydrophobic transmembrane domains, interact with guanine nucleotide binding regulatory proteins, and detect molecules outside the cell and act to transduce these signals into intracellular responses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]","start":47685864,"end":47722021,"strand":1,"description":"adhesion G protein-coupled receptor F4 [Source:HGNC Symbol;Acc:HGNC:19011]"}, {"versioned_ensembl_gene_id":"ENSG00000229345.1","gene_symbol":"AL392185.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95599545,"end":95606286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121594.11","gene_symbol":"CD80","gene_name":"CD80 molecule [Source:HGNC Symbol;Acc:HGNC:1700]","synonyms":"CD28LG1,CD28LG,B7.1,B7-1","biotype":"protein_coding","ncbi_id":"941","summary":"The protein encoded by this gene is a membrane receptor that is activated by the binding of CD28 or CTLA-4. The activated protein induces T-cell proliferation and cytokine production. This protein can act as a receptor for adenovirus subgroup B and may play a role in lupus neuropathy. [provided by RefSeq, Aug 2011]","start":119524293,"end":119559602,"strand":-1,"description":"CD80 molecule [Source:HGNC Symbol;Acc:HGNC:1700]"}, {"versioned_ensembl_gene_id":"ENSG00000227358.1","gene_symbol":"AL354861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95652912,"end":95653266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144848.10","gene_symbol":"ATG3","gene_name":"autophagy related 3 [Source:HGNC Symbol;Acc:HGNC:20962]","synonyms":"PC3-96,MGC15201,FLJ22125,DKFZp564M1178,APG3L","biotype":"protein_coding","ncbi_id":"64422","summary":"This gene encodes a ubiquitin-like-conjugating enzyme and is a component of ubiquitination-like systems involved in autophagy, the process of degradation, turnover and recycling of cytoplasmic constituents in eukaryotic cells. This protein is known to play a role in regulation of autophagy during cell death. A pseudogene of this gene is located on chromosome 20. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":112532509,"end":112562046,"strand":-1,"description":"autophagy related 3 [Source:HGNC Symbol;Acc:HGNC:20962]"}, {"versioned_ensembl_gene_id":"ENSG00000226220.1","gene_symbol":"CICP22","gene_name":"capicua transcriptional repressor pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:48838]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288083","summary":null,"start":39796593,"end":39797911,"strand":-1,"description":"capicua transcriptional repressor pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:48838]"}, {"versioned_ensembl_gene_id":"ENSG00000255084.1","gene_symbol":"AP003110.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78533176,"end":78558565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238201.1","gene_symbol":"AC114752.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64338067,"end":64341647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228142.2","gene_symbol":"AL354861.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95650154,"end":95715718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236148.5","gene_symbol":"RPL23AP37","gene_name":"ribosomal protein L23a pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35664]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130773","summary":null,"start":64347193,"end":64347741,"strand":-1,"description":"ribosomal protein L23a pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:35664]"}, {"versioned_ensembl_gene_id":"ENSG00000137513.9","gene_symbol":"NARS2","gene_name":"asparaginyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:26274]","synonyms":"SLM5,FLJ23441,DFNB94","biotype":"protein_coding","ncbi_id":"79731","summary":"This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of asparagine to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 24 (COXPD24). [provided by RefSeq, Mar 2015]","start":78435961,"end":78574874,"strand":-1,"description":"asparaginyl-tRNA synthetase 2, mitochondrial (putative) [Source:HGNC Symbol;Acc:HGNC:26274]"}, {"versioned_ensembl_gene_id":"ENSG00000166133.17","gene_symbol":"RPUSD2","gene_name":"RNA pseudouridylate synthase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24180]","synonyms":"C18B11,C15orf19,FLJ31409","biotype":"protein_coding","ncbi_id":"27079","summary":null,"start":40569300,"end":40574943,"strand":1,"description":"RNA pseudouridylate synthase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24180]"}, {"versioned_ensembl_gene_id":"ENSG00000259813.1","gene_symbol":"AC138028.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88696501,"end":88698610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158717.10","gene_symbol":"RNF166","gene_name":"ring finger protein 166 [Source:HGNC Symbol;Acc:HGNC:28856]","synonyms":"MGC2647,MGC14381","biotype":"protein_coding","ncbi_id":"115992","summary":null,"start":88696495,"end":88706421,"strand":-1,"description":"ring finger protein 166 [Source:HGNC Symbol;Acc:HGNC:28856]"}, {"versioned_ensembl_gene_id":"ENSG00000236859.6","gene_symbol":"NIFK-AS1","gene_name":"NIFK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27385]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"254128","summary":null,"start":121649650,"end":121728481,"strand":1,"description":"NIFK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27385]"}, {"versioned_ensembl_gene_id":"ENSG00000164393.8","gene_symbol":"ADGRF2","gene_name":"adhesion G protein-coupled receptor F2 [Source:HGNC Symbol;Acc:HGNC:18991]","synonyms":"PGR20,hGPCR35,GPR111","biotype":"protein_coding","ncbi_id":"222611","summary":null,"start":47656436,"end":47697797,"strand":1,"description":"adhesion G protein-coupled receptor F2 [Source:HGNC Symbol;Acc:HGNC:18991]"}, {"versioned_ensembl_gene_id":"ENSG00000264340.1","gene_symbol":"AC009704.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74561381,"end":74562100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164466.12","gene_symbol":"SFXN1","gene_name":"sideroflexin 1 [Source:HGNC Symbol;Acc:HGNC:16085]","synonyms":"FLJ12876","biotype":"protein_coding","ncbi_id":"94081","summary":null,"start":175477062,"end":175529742,"strand":1,"description":"sideroflexin 1 [Source:HGNC Symbol;Acc:HGNC:16085]"}, {"versioned_ensembl_gene_id":"ENSG00000113845.9","gene_symbol":"TIMMDC1","gene_name":"translocase of inner mitochondrial membrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1321]","synonyms":"FLJ22597,C3orf1","biotype":"protein_coding","ncbi_id":"51300","summary":null,"start":119498532,"end":119525090,"strand":1,"description":"translocase of inner mitochondrial membrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1321]"}, {"versioned_ensembl_gene_id":"ENSG00000150656.14","gene_symbol":"CNDP1","gene_name":"carnosine dipeptidase 1 [Source:HGNC Symbol;Acc:HGNC:20675]","synonyms":"MGC10825,HsT2308,CPGL2,CN1","biotype":"protein_coding","ncbi_id":"84735","summary":"This gene encodes a member of the M20 metalloprotease family. The encoded protein is specifically expressed in the brain, is a homodimeric dipeptidase which was identified as human carnosinase. This gene contains trinucleotide (CTG) repeat length polymorphism in the coding region. [provided by RefSeq, Jul 2008]","start":74534440,"end":74587212,"strand":1,"description":"carnosine dipeptidase 1 [Source:HGNC Symbol;Acc:HGNC:20675]"}, {"versioned_ensembl_gene_id":"ENSG00000273356.1","gene_symbol":"LINC02019","gene_name":"long intergenic non-protein coding RNA 2019 [Source:HGNC Symbol;Acc:HGNC:52854]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986085","summary":null,"start":50669989,"end":50672048,"strand":1,"description":"long intergenic non-protein coding RNA 2019 [Source:HGNC Symbol;Acc:HGNC:52854]"}, {"versioned_ensembl_gene_id":"ENSG00000130305.16","gene_symbol":"NSUN5","gene_name":"NOP2/Sun RNA methyltransferase family member 5 [Source:HGNC Symbol;Acc:HGNC:16385]","synonyms":"WBSCR20A,WBSCR20,p120(NOL1),NSUN5A,NOL1R,FLJ10267,Ynl022cL","biotype":"protein_coding","ncbi_id":"55695","summary":"This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":73302517,"end":73308867,"strand":-1,"description":"NOP2/Sun RNA methyltransferase family member 5 [Source:HGNC Symbol;Acc:HGNC:16385]"}, {"versioned_ensembl_gene_id":"ENSG00000231198.1","gene_symbol":"AC004987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39833286,"end":39833793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268926.2","gene_symbol":"AL354861.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95772323,"end":95774734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175741.5","gene_symbol":"RWDD4P2","gene_name":"RWD domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23754]","synonyms":"FAM28CP","biotype":"processed_pseudogene","ncbi_id":"647009","summary":null,"start":39854494,"end":39855056,"strand":-1,"description":"RWD domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23754]"}, {"versioned_ensembl_gene_id":"ENSG00000237251.2","gene_symbol":"AC004987.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39816549,"end":39868140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182150.15","gene_symbol":"ERCC6L2","gene_name":"ERCC excision repair 6 like 2 [Source:HGNC Symbol;Acc:HGNC:26922]","synonyms":"RAD26L,FLJ37706,C9orf102","biotype":"protein_coding","ncbi_id":"375748","summary":"This gene encodes a member of the Snf2 family of helicase-like proteins. The encoded protein may play a role in DNA repair and mitochondrial function. Mutations in this gene have been associated with bone marrow failure syndrome 2. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Apr 2014]","start":95875701,"end":96014571,"strand":1,"description":"ERCC excision repair 6 like 2 [Source:HGNC Symbol;Acc:HGNC:26922]"}, {"versioned_ensembl_gene_id":"ENSG00000237631.2","gene_symbol":"AL161454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95918136,"end":95918704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175611.11","gene_symbol":"LINC00476","gene_name":"long intergenic non-protein coding RNA 476 [Source:HGNC Symbol;Acc:HGNC:27858]","synonyms":"C9orf130","biotype":"processed_transcript","ncbi_id":"100128782","summary":null,"start":95759231,"end":95875977,"strand":-1,"description":"long intergenic non-protein coding RNA 476 [Source:HGNC Symbol;Acc:HGNC:27858]"}, {"versioned_ensembl_gene_id":"ENSG00000270839.1","gene_symbol":"AC091393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175483595,"end":175484192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119523.9","gene_symbol":"ALG2","gene_name":"ALG2, alpha-1,3/1,6-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:23159]","synonyms":"CDGIi,CDG1I,NET38,hALPG2,FLJ14511","biotype":"protein_coding","ncbi_id":"85365","summary":"This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":99216426,"end":99221956,"strand":-1,"description":"ALG2, alpha-1,3/1,6-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:23159]"}, {"versioned_ensembl_gene_id":"ENSG00000169435.13","gene_symbol":"RASSF6","gene_name":"Ras association domain family member 6 [Source:HGNC Symbol;Acc:HGNC:20796]","synonyms":null,"biotype":"protein_coding","ncbi_id":"166824","summary":"This gene encodes a member of the Ras-association domain family (RASSF). Members of this family form the core of a highly conserved tumor suppressor network, the Salvador-Warts-Hippo (SWH) pathway. The protein encoded by this gene is a Ras effector protein that induces apoptosis. A genomic region containing this gene has been linked to susceptibility to viral bronchiolitis. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":73571550,"end":73620631,"strand":-1,"description":"Ras association domain family member 6 [Source:HGNC Symbol;Acc:HGNC:20796]"}, {"versioned_ensembl_gene_id":"ENSG00000225142.2","gene_symbol":"AC114495.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31108188,"end":31108623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230444.1","gene_symbol":"TFAMP1","gene_name":"transcription factor A, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11636]","synonyms":"TCF6L1,MTTF1","biotype":"processed_pseudogene","ncbi_id":"260341","summary":null,"start":1614590,"end":1615325,"strand":1,"description":"transcription factor A, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11636]"}, {"versioned_ensembl_gene_id":"ENSG00000173442.12","gene_symbol":"EHBP1L1","gene_name":"EH domain binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:30682]","synonyms":"TANGERIN,DKFZp762C186","biotype":"protein_coding","ncbi_id":"254102","summary":null,"start":65576038,"end":65592650,"strand":1,"description":"EH domain binding protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:30682]"}, {"versioned_ensembl_gene_id":"ENSG00000251330.3","gene_symbol":"AC114939.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148430159,"end":148430807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237217.1","gene_symbol":"AC008074.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64450096,"end":64450524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223935.1","gene_symbol":"AC008074.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64395220,"end":64453798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153879.8","gene_symbol":"CEBPG","gene_name":"CCAAT/enhancer binding protein gamma [Source:HGNC Symbol;Acc:HGNC:1837]","synonyms":"IG/EBP-1,GPE1BP","biotype":"protein_coding","ncbi_id":"1054","summary":"The C/EBP family of transcription factors regulates viral and cellular CCAAT/enhancer element-mediated transcription. C/EBP proteins contain the bZIP region, which is characterized by two motifs in the C-terminal half of the protein: a basic region involved in DNA binding and a leucine zipper motif involved in dimerization. The C/EBP family consist of several related proteins, C/EBP alpha, C/EBP beta, C/EBP gamma, and C/EBP delta, that form homodimers and that form heterodimers with each other. CCAAT/enhancer binding protein gamma may cooperate with Fos to bind PRE-I enhancer elements. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2011]","start":33373330,"end":33382686,"strand":1,"description":"CCAAT/enhancer binding protein gamma [Source:HGNC Symbol;Acc:HGNC:1837]"}, {"versioned_ensembl_gene_id":"ENSG00000250234.1","gene_symbol":"AC025754.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34656412,"end":34657250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248405.10","gene_symbol":"PRR5-ARHGAP8","gene_name":"PRR5-ARHGAP8 readthrough [Source:HGNC Symbol;Acc:HGNC:34512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"553158","summary":"The PRR5-ARHGAP8 mRNA is an infrequent but naturally occurring read-through transcript of the neighboring proline rich 5, renal (PRR5) and Rho GTPase activating protein 8 (ARHGAP8) genes. The resulting fusion protein contains sequence identity with each individual gene product, and it includes domains characteristic of a RhoGAP protein. The significance of this read-through transcript and the function of its protein product have not yet been determined. [provided by RefSeq, Nov 2010]","start":44702233,"end":44862706,"strand":1,"description":"PRR5-ARHGAP8 readthrough [Source:HGNC Symbol;Acc:HGNC:34512]"}, {"versioned_ensembl_gene_id":"ENSG00000197816.13","gene_symbol":"CCDC180","gene_name":"coiled-coil domain containing 180 [Source:HGNC Symbol;Acc:HGNC:29303]","synonyms":"KIAA1529,DKFZp434I2420,C9orf174,BDAG1","biotype":"protein_coding","ncbi_id":"100499483","summary":"The protein encoded by this gene contains a coiled-coil domain. Alternative splicing results in multiple transcript variants encoding different isoforms. A single nucleotide polymorphism (SNP) in this gene has been associated with increased susceptibility to Behcet's Disease (PMID: 19442274). [provided by RefSeq, Dec 2016]","start":97307304,"end":97378524,"strand":1,"description":"coiled-coil domain containing 180 [Source:HGNC Symbol;Acc:HGNC:29303]"}, {"versioned_ensembl_gene_id":"ENSG00000165275.9","gene_symbol":"TRMT10B","gene_name":"tRNA methyltransferase 10B [Source:HGNC Symbol;Acc:HGNC:26454]","synonyms":"RG9MTD3,FLJ31455,bA3J10.9","biotype":"protein_coding","ncbi_id":"158234","summary":null,"start":37753803,"end":37778972,"strand":1,"description":"tRNA methyltransferase 10B [Source:HGNC Symbol;Acc:HGNC:26454]"}, {"versioned_ensembl_gene_id":"ENSG00000198133.8","gene_symbol":"TMEM229B","gene_name":"transmembrane protein 229B [Source:HGNC Symbol;Acc:HGNC:20130]","synonyms":"FLJ33387,C14orf83","biotype":"protein_coding","ncbi_id":"161145","summary":null,"start":67447084,"end":67533739,"strand":-1,"description":"transmembrane protein 229B [Source:HGNC Symbol;Acc:HGNC:20130]"}, {"versioned_ensembl_gene_id":"ENSG00000099622.13","gene_symbol":"CIRBP","gene_name":"cold inducible RNA binding protein [Source:HGNC Symbol;Acc:HGNC:1982]","synonyms":"CIRP","biotype":"protein_coding","ncbi_id":"1153","summary":null,"start":1259384,"end":1274880,"strand":1,"description":"cold inducible RNA binding protein [Source:HGNC Symbol;Acc:HGNC:1982]"}, {"versioned_ensembl_gene_id":"ENSG00000183918.15","gene_symbol":"SH2D1A","gene_name":"SH2 domain containing 1A [Source:HGNC Symbol;Acc:HGNC:10820]","synonyms":"XLPD,XLP,SAP,MTCP1,LYP,IMD5,EBVS,DSHP","biotype":"protein_coding","ncbi_id":"4068","summary":"This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells. This protein contains an SH2 domain and a short tail. It associates with the signaling lymphocyte-activation molecule, thereby acting as an inhibitor of this transmembrane protein by blocking the recruitment of the SH2-domain-containing signal-transduction molecule SHP-2 to its docking site. This protein can also bind to other related surface molecules that are expressed on activated T, B and NK cells, thereby modifying signal transduction pathways in these cells. Mutations in this gene cause lymphoproliferative syndrome X-linked type 1 or Duncan disease, a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus, with symptoms including severe mononucleosis and malignant lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":124227868,"end":124373197,"strand":1,"description":"SH2 domain containing 1A [Source:HGNC Symbol;Acc:HGNC:10820]"}, {"versioned_ensembl_gene_id":"ENSG00000236345.1","gene_symbol":"AL354719.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63806836,"end":63822642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112077.15","gene_symbol":"RHAG","gene_name":"Rh-associated glycoprotein [Source:HGNC Symbol;Acc:HGNC:10006]","synonyms":"SLC42A1,RH50A,CD241","biotype":"protein_coding","ncbi_id":"6005","summary":"The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009]","start":49605158,"end":49636839,"strand":-1,"description":"Rh-associated glycoprotein [Source:HGNC Symbol;Acc:HGNC:10006]"}, {"versioned_ensembl_gene_id":"ENSG00000258173.1","gene_symbol":"AC079598.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87753414,"end":87753447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170390.15","gene_symbol":"DCLK2","gene_name":"doublecortin like kinase 2 [Source:HGNC Symbol;Acc:HGNC:19002]","synonyms":"DCDC3B,DCDC3,DCAMKL2,MGC45428,DCK2","biotype":"protein_coding","ncbi_id":"166614","summary":"This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. Mouse studies show that the DCX gene, another family member, and this gene share function in the establishment of hippocampal organization and that their absence results in a severe epileptic phenotype and lethality, as described in human patients with lissencephaly. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Sep 2010]","start":150078274,"end":150257457,"strand":1,"description":"doublecortin like kinase 2 [Source:HGNC Symbol;Acc:HGNC:19002]"}, {"versioned_ensembl_gene_id":"ENSG00000116157.5","gene_symbol":"GPX7","gene_name":"glutathione peroxidase 7 [Source:HGNC Symbol;Acc:HGNC:4559]","synonyms":"NPGPx,GPX6,FLJ14777","biotype":"protein_coding","ncbi_id":"2882","summary":null,"start":52602372,"end":52609051,"strand":1,"description":"glutathione peroxidase 7 [Source:HGNC Symbol;Acc:HGNC:4559]"}, {"versioned_ensembl_gene_id":"ENSG00000227507.2","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31580525,"end":31582522,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000229541.2","gene_symbol":"GAPDHP26","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37778]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392374","summary":null,"start":100975668,"end":100976682,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37778]"}, {"versioned_ensembl_gene_id":"ENSG00000271383.6","gene_symbol":"NBPF19","gene_name":"NBPF member 19 [Source:HGNC Symbol;Acc:HGNC:31999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060226","summary":null,"start":149390623,"end":149556361,"strand":1,"description":"NBPF member 19 [Source:HGNC Symbol;Acc:HGNC:31999]"}, {"versioned_ensembl_gene_id":"ENSG00000171201.10","gene_symbol":"SMR3B","gene_name":"submaxillary gland androgen regulated protein 3B [Source:HGNC Symbol;Acc:HGNC:17326]","synonyms":"PROL3,PRL3,P-B","biotype":"protein_coding","ncbi_id":"10879","summary":null,"start":70370093,"end":70390244,"strand":1,"description":"submaxillary gland androgen regulated protein 3B [Source:HGNC Symbol;Acc:HGNC:17326]"}, {"versioned_ensembl_gene_id":"ENSG00000156052.10","gene_symbol":"GNAQ","gene_name":"G protein subunit alpha q [Source:HGNC Symbol;Acc:HGNC:4390]","synonyms":"GAQ,G-ALPHA-q","biotype":"protein_coding","ncbi_id":"2776","summary":"This locus encodes a guanine nucleotide-binding protein. The encoded protein, an alpha subunit in the Gq class, couples a seven-transmembrane domain receptor to activation of phospolipase C-beta. Mutations at this locus have been associated with problems in platelet activation and aggregation. A related pseudogene exists on chromosome 2.[provided by RefSeq, Nov 2010]","start":77716087,"end":78031458,"strand":-1,"description":"G protein subunit alpha q [Source:HGNC Symbol;Acc:HGNC:4390]"}, {"versioned_ensembl_gene_id":"ENSG00000253205.5","gene_symbol":"AC011124.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63384839,"end":63470205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255102.1","gene_symbol":"AP005436.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88061774,"end":88098147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269749.1","gene_symbol":"AC005614.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":40048757,"end":40090925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184465.15","gene_symbol":"WDR27","gene_name":"WD repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:21248]","synonyms":"MGC43690","biotype":"protein_coding","ncbi_id":"253769","summary":"This gene encodes a protein with multiple WD repeats. Proteins with these repeats may form scaffolds for protein-protein interaction and play key roles in cell signalling. Alternative splicing results in multiple transcript variants, but the full-length structure of some of these variants cannot be determined. [provided by RefSeq, Nov 2015]","start":169457212,"end":169702048,"strand":-1,"description":"WD repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:21248]"}, {"versioned_ensembl_gene_id":"ENSG00000261158.1","gene_symbol":"AC109597.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12759282,"end":12761162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265015.1","gene_symbol":"AP005901.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":15196999,"end":15197775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273083.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"NOL5BP,NOL5B,NOP56-L,dJ207F6.1","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783623,"end":28783994,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000167705.11","gene_symbol":"RILP","gene_name":"Rab interacting lysosomal protein [Source:HGNC Symbol;Acc:HGNC:30266]","synonyms":"FLJ31193","biotype":"protein_coding","ncbi_id":"83547","summary":"This gene encodes a lysosomal protein that interacts with RAB7, a small GTPase that controls transport to endocytic degradative compartments. Studies using mutant forms of the two proteins suggest that this protein represents a downstream effector for RAB7, and both proteins act together in the regulation of late endocytic traffic. A unique region of this protein has also been shown to be involved in the regulation of lysosomal morphology. [provided by RefSeq, Sep 2011]","start":1646145,"end":1650077,"strand":-1,"description":"Rab interacting lysosomal protein [Source:HGNC Symbol;Acc:HGNC:30266]"}, {"versioned_ensembl_gene_id":"ENSG00000013619.13","gene_symbol":"MAMLD1","gene_name":"mastermind like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:2568]","synonyms":"CG1,F18,CXorf6","biotype":"protein_coding","ncbi_id":"10046","summary":"This gene encodes a mastermind-like domain containing protein. This protein may function as a transcriptional co-activator. Mutations in this gene are the cause of X-linked hypospadias type 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":150361422,"end":150514178,"strand":1,"description":"mastermind like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:2568]"}, {"versioned_ensembl_gene_id":"ENSG00000277527.1","gene_symbol":"LINC01796","gene_name":"long intergenic non-protein coding RNA 1796 [Source:HGNC Symbol;Acc:HGNC:52586]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373518","summary":null,"start":102873339,"end":102895722,"strand":-1,"description":"long intergenic non-protein coding RNA 1796 [Source:HGNC Symbol;Acc:HGNC:52586]"}, {"versioned_ensembl_gene_id":"ENSG00000102554.13","gene_symbol":"KLF5","gene_name":"Kruppel like factor 5 [Source:HGNC Symbol;Acc:HGNC:6349]","synonyms":"IKLF,CKLF,BTEB2","biotype":"protein_coding","ncbi_id":"688","summary":"This gene encodes a member of the Kruppel-like factor subfamily of zinc finger proteins. The encoded protein is a transcriptional activator that binds directly to a specific recognition motif in the promoters of target genes. This protein acts downstream of multiple different signaling pathways and is regulated by post-translational modification. It may participate in both promoting and suppressing cell proliferation. Expression of this gene may be changed in a variety of different cancers and in cardiovascular disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":73054976,"end":73077542,"strand":1,"description":"Kruppel like factor 5 [Source:HGNC Symbol;Acc:HGNC:6349]"}, {"versioned_ensembl_gene_id":"ENSG00000186119.8","gene_symbol":"OR5D18","gene_name":"olfactory receptor family 5 subfamily D member 18 [Source:HGNC Symbol;Acc:HGNC:15285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219438","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55819607,"end":55820597,"strand":1,"description":"olfactory receptor family 5 subfamily D member 18 [Source:HGNC Symbol;Acc:HGNC:15285]"}, {"versioned_ensembl_gene_id":"ENSG00000186113.1","gene_symbol":"OR5D14","gene_name":"olfactory receptor family 5 subfamily D member 14 [Source:HGNC Symbol;Acc:HGNC:15281]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219436","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55795556,"end":55796500,"strand":1,"description":"olfactory receptor family 5 subfamily D member 14 [Source:HGNC Symbol;Acc:HGNC:15281]"}, {"versioned_ensembl_gene_id":"ENSG00000236079.1","gene_symbol":"Z85994.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44413485,"end":44414814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106366.8","gene_symbol":"SERPINE1","gene_name":"serpin family E member 1 [Source:HGNC Symbol;Acc:HGNC:8583]","synonyms":"PLANH1,PAI1,PAI","biotype":"protein_coding","ncbi_id":"5054","summary":"This gene encodes a member of the serine proteinase inhibitor (serpin) superfamily. This member is the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), and hence is an inhibitor of fibrinolysis. The protein also functions as a component of innate antiviral immunity. Defects in this gene are the cause of plasminogen activator inhibitor-1 deficiency (PAI-1 deficiency), and high concentrations of the gene product are associated with thrombophilia. [provided by RefSeq, Aug 2020]","start":101127089,"end":101139266,"strand":1,"description":"serpin family E member 1 [Source:HGNC Symbol;Acc:HGNC:8583]"}, {"versioned_ensembl_gene_id":"ENSG00000256875.2","gene_symbol":"AC079031.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132462242,"end":132462856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175054.14","gene_symbol":"ATR","gene_name":"ATR serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:882]","synonyms":"SCKL1,SCKL,MEC1,FRP1","biotype":"protein_coding","ncbi_id":"545","summary":"The protein encoded by this gene is a serine/threonine kinase and DNA damage sensor, activating cell cycle checkpoint signaling upon DNA stress. The encoded protein can phosphorylate and activate several proteins involved in the inhibition of DNA replication and mitosis, and can promote DNA repair, recombination, and apoptosis. This protein is also important for fragile site stability and centrosome duplication. Defects in this gene are a cause of Seckel syndrome 1. [provided by RefSeq, Aug 2017]","start":142449235,"end":142578826,"strand":-1,"description":"ATR serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:882]"}, {"versioned_ensembl_gene_id":"ENSG00000242479.1","gene_symbol":"AC109992.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142450102,"end":142452149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254017.1","gene_symbol":"IGHEP2","gene_name":"immunoglobulin heavy constant epsilon P2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5524]","synonyms":null,"biotype":"IG_C_pseudogene","ncbi_id":"3499","summary":null,"start":5113549,"end":5114804,"strand":1,"description":"immunoglobulin heavy constant epsilon P2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5524]"}, {"versioned_ensembl_gene_id":"ENSG00000228166.1","gene_symbol":"MTND1P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42060]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873212","summary":null,"start":5094139,"end":5095014,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42060]"}, {"versioned_ensembl_gene_id":"ENSG00000268845.1","gene_symbol":"AC025278.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6953211,"end":6954904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273447.1","gene_symbol":"AC004067.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109692004,"end":109692703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283131.1","gene_symbol":"MTND2P41","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52317]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729121","summary":null,"start":68049706,"end":68050478,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52317]"}, {"versioned_ensembl_gene_id":"ENSG00000275503.1","gene_symbol":"AL355994.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15989140,"end":15989375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231353.1","gene_symbol":"AL355994.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15988182,"end":15988441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220702.1","gene_symbol":"Z85994.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44365551,"end":44366284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267244.5","gene_symbol":"AC012615.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1822089,"end":1824542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233834.6","gene_symbol":"AC005083.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":20217577,"end":20221700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006283.17","gene_symbol":"CACNA1G","gene_name":"calcium voltage-gated channel subunit alpha1 G [Source:HGNC Symbol;Acc:HGNC:1394]","synonyms":"NBR13,Cav3.1","biotype":"protein_coding","ncbi_id":"8913","summary":"Voltage-sensitive calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division, and cell death. This gene encodes a T-type, low-voltage activated calcium channel. The T-type channels generate currents that are both transient, owing to fast inactivation, and tiny, owing to small conductance. T-type channels are thought to be involved in pacemaker activity, low-threshold calcium spikes, neuronal oscillations and resonance, and rebound burst firing. Many alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Sep 2011]","start":50561068,"end":50627474,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 G [Source:HGNC Symbol;Acc:HGNC:1394]"}, {"versioned_ensembl_gene_id":"ENSG00000254928.1","gene_symbol":"AP001372.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74455348,"end":74456825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142920.16","gene_symbol":"AZIN2","gene_name":"antizyme inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:29957]","synonyms":"ODCp,ODC1L,ODC-p,KIAA1945,ADC","biotype":"protein_coding","ncbi_id":"113451","summary":"The protein encoded by this gene belongs to the antizyme inhibitor family, which plays a role in cell growth and proliferation by maintaining polyamine homeostasis within the cell. Antizyme inhibitors are homologs of ornithine decarboxylase (ODC, the key enzyme in polyamine biosynthesis) that have lost the ability to decarboxylase ornithine; however, retain the ability to bind to antizymes. Antizymes negatively regulate intracellular polyamine levels by binding to ODC and targeting it for degradation, as well as by inhibiting polyamine uptake. Antizyme inhibitors function as positive regulators of polyamine levels by sequestering antizymes and neutralizing their effect. This gene encodes antizyme inhibitor 2, the second member of this gene family. Like antizyme inhibitor 1, antizyme inhibitor 2 interacts with all 3 antizymes and stimulates ODC activity and polyamine uptake. However, unlike antizyme inhibitor 1, which is ubiquitously expressed and localized in the nucleus and cytoplasm, antizyme inhibitor 2 is predominantly expressed in the brain and testis and localized in the endoplasmic reticulum-golgi intermediate compartment. Recent studies indicate that antizyme inhibitor 2 is also expressed in specific cell types in ovaries, adrenal glands and pancreas, and in mast cells. The exact function of this gene is not known, however, available data suggest its role in cell growth, spermiogenesis, vesicular trafficking and secretion. Accumulation of antizyme inhibitor 2 has also been observed in brains of patients with Alzheimer's disease. There has been confusion in literature and databases over the nomenclature of this gene, stemming from an earlier report that a human cDNA clone (identical to ODCp/AZIN2) had arginine decarboxylase (ADC) activity (PMID:14738999). Subsequent studies in human and mouse showed that antizyme inhibitor 2 was devoid of arginine decarboxylase activity (PMID:19956990). Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2014]","start":33081104,"end":33120530,"strand":1,"description":"antizyme inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:29957]"}, {"versioned_ensembl_gene_id":"ENSG00000249520.1","gene_symbol":"AC093824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185064981,"end":185065323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081386.12","gene_symbol":"ZNF510","gene_name":"zinc finger protein 510 [Source:HGNC Symbol;Acc:HGNC:29161]","synonyms":"KIAA0972","biotype":"protein_coding","ncbi_id":"22869","summary":"This gene encodes a krueppel C2H2-type zinc-finger protein family member. The encoded protein is expressed in several cancer cell types and may be a biomarker for early diagnosis of these cancers. [provided by RefSeq, Sep 2015]","start":96755865,"end":96778129,"strand":-1,"description":"zinc finger protein 510 [Source:HGNC Symbol;Acc:HGNC:29161]"}, {"versioned_ensembl_gene_id":"ENSG00000231789.2","gene_symbol":"PIK3CD-AS2","gene_name":"PIK3CD antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51334]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929074","summary":null,"start":9672426,"end":9687555,"strand":-1,"description":"PIK3CD antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51334]"}, {"versioned_ensembl_gene_id":"ENSG00000270716.1","gene_symbol":"BNIP3P15","gene_name":"BCL2 interacting protein 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481692","summary":null,"start":20136933,"end":20137233,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49695]"}, {"versioned_ensembl_gene_id":"ENSG00000064933.17","gene_symbol":"PMS1","gene_name":"PMS1 homolog 1, mismatch repair system component [Source:HGNC Symbol;Acc:HGNC:9121]","synonyms":"PMSL1,MLH2","biotype":"protein_coding","ncbi_id":"5378","summary":"This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. [provided by RefSeq, Jul 2008]","start":189784085,"end":189877629,"strand":1,"description":"PMS1 homolog 1, mismatch repair system component [Source:HGNC Symbol;Acc:HGNC:9121]"}, {"versioned_ensembl_gene_id":"ENSG00000240673.1","gene_symbol":"AC006539.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20079818,"end":20080539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267771.1","gene_symbol":"AC011447.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20206844,"end":20206954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154252.11","gene_symbol":"GAL3ST2","gene_name":"galactose-3-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:24869]","synonyms":"GP3ST","biotype":"protein_coding","ncbi_id":"64090","summary":"This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the hydroxyl at C-3 of nonreducing beta-galactosyl residues, and it can act on both type 1 and type 2 (Galbeta 1-3/1-4GlcNAc-R) oligosaccharides with similar efficiencies, and on core 1 glycans. This enzyme has been implicated in tumor metastasis processes. This gene is different from the GAL3ST3 gene located on chromosome 11, which has also been referred to as GAL3ST2 and encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 2. [provided by RefSeq, Jul 2008]","start":241776825,"end":241804208,"strand":1,"description":"galactose-3-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:24869]"}, {"versioned_ensembl_gene_id":"ENSG00000226753.1","gene_symbol":"AL451105.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75888700,"end":75888888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213985.4","gene_symbol":"AC078899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20257720,"end":20259418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229090.2","gene_symbol":"FO082842.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101720340,"end":101721709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274612.1","gene_symbol":"AC011447.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20087013,"end":20087576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241582.1","gene_symbol":"RPL23AP8","gene_name":"ribosomal protein L23a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23543]","synonyms":"RPL23AP9","biotype":"processed_pseudogene","ncbi_id":"641614","summary":null,"start":34694170,"end":34694644,"strand":1,"description":"ribosomal protein L23a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23543]"}, {"versioned_ensembl_gene_id":"ENSG00000256273.1","gene_symbol":"AC022511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68344664,"end":68349959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214561.3","gene_symbol":"RBBP4P4","gene_name":"RB binding protein 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727842","summary":null,"start":58119741,"end":58121029,"strand":-1,"description":"RB binding protein 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42371]"}, {"versioned_ensembl_gene_id":"ENSG00000233037.2","gene_symbol":"AC009237.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95542730,"end":95543230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168303.6","gene_symbol":"MPLKIP","gene_name":"M-phase specific PLK1 interacting protein [Source:HGNC Symbol;Acc:HGNC:16002]","synonyms":"TTDN1,ORF20,C7orf11","biotype":"protein_coding","ncbi_id":"136647","summary":"The protein encoded by this gene localizes to the centrosome during mitosis and to the midbody during cytokinesis. The protein is phosphorylated by cyclin-dependent kinase 1 during mitosis and subsequently interacts with polo-like kinase 1. The protein is thought to function in regulating mitosis and cytokinesis. Mutations in this gene result in nonphotosensitive trichothiodystrophy. [provided by RefSeq, Nov 2009]","start":40126023,"end":40134659,"strand":-1,"description":"M-phase specific PLK1 interacting protein [Source:HGNC Symbol;Acc:HGNC:16002]"}, {"versioned_ensembl_gene_id":"ENSG00000223628.2","gene_symbol":"AC023449.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25580969,"end":25581122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171209.3","gene_symbol":"CSN3","gene_name":"casein kappa [Source:HGNC Symbol;Acc:HGNC:2446]","synonyms":"CSN10","biotype":"protein_coding","ncbi_id":"1448","summary":null,"start":70242588,"end":70251428,"strand":1,"description":"casein kappa [Source:HGNC Symbol;Acc:HGNC:2446]"}, {"versioned_ensembl_gene_id":"ENSG00000253521.1","gene_symbol":"HPYR1","gene_name":"Helicobacter pylori responsive 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16071]","synonyms":"NCRNA00027,LINC00027,HPRG1","biotype":"lincRNA","ncbi_id":"93668","summary":null,"start":132560498,"end":132561479,"strand":-1,"description":"Helicobacter pylori responsive 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16071]"}, {"versioned_ensembl_gene_id":"ENSG00000165434.7","gene_symbol":"PGM2L1","gene_name":"phosphoglucomutase 2 like 1 [Source:HGNC Symbol;Acc:HGNC:20898]","synonyms":"FLJ32029,BM32A","biotype":"protein_coding","ncbi_id":"283209","summary":null,"start":74330318,"end":74398473,"strand":-1,"description":"phosphoglucomutase 2 like 1 [Source:HGNC Symbol;Acc:HGNC:20898]"}, {"versioned_ensembl_gene_id":"ENSG00000082458.11","gene_symbol":"DLG3","gene_name":"discs large MAGUK scaffold protein 3 [Source:HGNC Symbol;Acc:HGNC:2902]","synonyms":"SAP102,SAP-102,PPP1R82,NEDLG,NE-Dlg,MRX90,KIAA1232","biotype":"protein_coding","ncbi_id":"1741","summary":"This gene encodes a member of the membrane-associated guanylate kinase protein family. The encoded protein may play a role in clustering of NMDA receptors at excitatory synapses. It may also negatively regulate cell proliferation through interaction with the C-terminal region of the adenomatosis polyposis coli tumor suppressor protein. Mutations in this gene have been associated with X-linked cognitive disability. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009]","start":70444861,"end":70505490,"strand":1,"description":"discs large MAGUK scaffold protein 3 [Source:HGNC Symbol;Acc:HGNC:2902]"}, {"versioned_ensembl_gene_id":"ENSG00000277743.1","gene_symbol":"AP005212.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14346214,"end":14346923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005436.13","gene_symbol":"GCFC2","gene_name":"GC-rich sequence DNA-binding factor 2 [Source:HGNC Symbol;Acc:HGNC:1317]","synonyms":"TCF9,GCF,DNABF,C2orf3","biotype":"protein_coding","ncbi_id":"6936","summary":"The first mRNA transcript isolated for this gene was part of an artificial chimera derived from two distinct gene transcripts and a primer used in the cloning process (see Genbank accession M29204). A positively charged amino terminus present only in the chimera was determined to bind GC-rich DNA, thus mistakenly thought to identify a transcription factor gene. [provided by RefSeq, Jul 2008]","start":75652000,"end":75710989,"strand":-1,"description":"GC-rich sequence DNA-binding factor 2 [Source:HGNC Symbol;Acc:HGNC:1317]"}, {"versioned_ensembl_gene_id":"ENSG00000250976.1","gene_symbol":"AC021491.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50563203,"end":50563783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270462.1","gene_symbol":"AC005034.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75697583,"end":75697996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271452.1","gene_symbol":"AC005034.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75669989,"end":75670454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257075.1","gene_symbol":"RPEP6","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44525]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420590","summary":null,"start":72131282,"end":72131907,"strand":1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44525]"}, {"versioned_ensembl_gene_id":"ENSG00000250107.1","gene_symbol":"CACNA1G-AS1","gene_name":"CACNA1G antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27377]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"253962","summary":null,"start":50556207,"end":50562108,"strand":-1,"description":"CACNA1G antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27377]"}, {"versioned_ensembl_gene_id":"ENSG00000157895.11","gene_symbol":"C12orf43","gene_name":"chromosome 12 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:25719]","synonyms":"FLJ12448","biotype":"protein_coding","ncbi_id":"64897","summary":null,"start":121000486,"end":121016502,"strand":-1,"description":"chromosome 12 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:25719]"}, {"versioned_ensembl_gene_id":"ENSG00000226360.5","gene_symbol":"AC096919.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61742455,"end":61743106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264107.1","gene_symbol":"AC138207.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31090787,"end":31095450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259258.1","gene_symbol":"AC013553.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65105534,"end":65105800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246922.8","gene_symbol":"UBAP1L","gene_name":"ubiquitin associated protein 1 like [Source:HGNC Symbol;Acc:HGNC:40028]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390595","summary":null,"start":65092770,"end":65115197,"strand":-1,"description":"ubiquitin associated protein 1 like [Source:HGNC Symbol;Acc:HGNC:40028]"}, {"versioned_ensembl_gene_id":"ENSG00000255077.1","gene_symbol":"AP005639.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55411526,"end":55411717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181958.4","gene_symbol":"OR4A15","gene_name":"olfactory receptor family 4 subfamily A member 15 [Source:HGNC Symbol;Acc:HGNC:15152]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81328","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55367884,"end":55368918,"strand":1,"description":"olfactory receptor family 4 subfamily A member 15 [Source:HGNC Symbol;Acc:HGNC:15152]"}, {"versioned_ensembl_gene_id":"ENSG00000250354.1","gene_symbol":"AC069272.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148146471,"end":148208880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181961.4","gene_symbol":"OR4A16","gene_name":"olfactory receptor family 4 subfamily A member 16 [Source:HGNC Symbol;Acc:HGNC:15153]","synonyms":"OR4A16Q","biotype":"protein_coding","ncbi_id":"81327","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55343151,"end":55344231,"strand":1,"description":"olfactory receptor family 4 subfamily A member 16 [Source:HGNC Symbol;Acc:HGNC:15153]"}, {"versioned_ensembl_gene_id":"ENSG00000278737.1","gene_symbol":"AC013553.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65083042,"end":65083663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279525.1","gene_symbol":"AC002451.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":95542145,"end":95544542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234438.3","gene_symbol":"KBTBD13","gene_name":"kelch repeat and BTB domain containing 13 [Source:HGNC Symbol;Acc:HGNC:37227]","synonyms":"NEM6,hCG_1645727","biotype":"protein_coding","ncbi_id":"390594","summary":"The gene belongs to a family of genes encoding proteins containing a BTB domain and several kelch repeats. The BTB domain functions as a protein-protein interaction module, which includes an ability to self-associate or to interact with non-BTB domain-containing proteins. The kelch motif typically occurs in groups of five to seven repeats, and has been found in proteins with diverse functions. Known functions of these family members include transcription regulation, ion channel tetramerization and gating, protein ubiquitination or degradation, and cytoskeleton regulation. The exact function of this family member has yet to be determined. [provided by RefSeq, Jun 2010]","start":65076816,"end":65078192,"strand":1,"description":"kelch repeat and BTB domain containing 13 [Source:HGNC Symbol;Acc:HGNC:37227]"}, {"versioned_ensembl_gene_id":"ENSG00000118518.15","gene_symbol":"RNF146","gene_name":"ring finger protein 146 [Source:HGNC Symbol;Acc:HGNC:21336]","synonyms":"DKFZp434O1427,dJ351K20.1,dactylidin","biotype":"protein_coding","ncbi_id":"81847","summary":null,"start":127266610,"end":127288567,"strand":1,"description":"ring finger protein 146 [Source:HGNC Symbol;Acc:HGNC:21336]"}, {"versioned_ensembl_gene_id":"ENSG00000266538.1","gene_symbol":"AC005838.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15530773,"end":15531089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152785.6","gene_symbol":"BMP3","gene_name":"bone morphogenetic protein 3 [Source:HGNC Symbol;Acc:HGNC:1070]","synonyms":null,"biotype":"protein_coding","ncbi_id":"651","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein suppresses osteoblast differentiation, and negatively regulates bone density, by modulating TGF-beta receptor availability to other ligands. [provided by RefSeq, Jul 2016]","start":81030965,"end":81057531,"strand":1,"description":"bone morphogenetic protein 3 [Source:HGNC Symbol;Acc:HGNC:1070]"}, {"versioned_ensembl_gene_id":"ENSG00000236761.5","gene_symbol":"CTAGE9","gene_name":"CTAGE family member 9 [Source:HGNC Symbol;Acc:HGNC:37275]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643854","summary":null,"start":131708684,"end":131711017,"strand":-1,"description":"CTAGE family member 9 [Source:HGNC Symbol;Acc:HGNC:37275]"}, {"versioned_ensembl_gene_id":"ENSG00000223878.1","gene_symbol":"AC005517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15506866,"end":15507354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182870.12","gene_symbol":"GALNT9","gene_name":"polypeptide N-acetylgalactosaminyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:4131]","synonyms":"GALNAC-T9","biotype":"protein_coding","ncbi_id":"50614","summary":"This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. This gene is expressed specifically in the brain, with highest expression in the cerebellum. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":132196372,"end":132329349,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:4131]"}, {"versioned_ensembl_gene_id":"ENSG00000260608.1","gene_symbol":"AC024270.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83012661,"end":83061845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100554.11","gene_symbol":"ATP6V1D","gene_name":"ATPase H+ transporting V1 subunit D [Source:HGNC Symbol;Acc:HGNC:13527]","synonyms":"VMA8,VATD,ATP6M","biotype":"protein_coding","ncbi_id":"51382","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes the V1 domain D subunit protein. [provided by RefSeq, Jul 2008]","start":67294371,"end":67360265,"strand":-1,"description":"ATPase H+ transporting V1 subunit D [Source:HGNC Symbol;Acc:HGNC:13527]"}, {"versioned_ensembl_gene_id":"ENSG00000227620.4","gene_symbol":"ALG1L8P","gene_name":"asparagine-linked glycosylation 1-like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:44377]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645015","summary":null,"start":67785273,"end":67792335,"strand":1,"description":"asparagine-linked glycosylation 1-like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:44377]"}, {"versioned_ensembl_gene_id":"ENSG00000256771.3","gene_symbol":"ZNF253","gene_name":"zinc finger protein 253 [Source:HGNC Symbol;Acc:HGNC:13497]","synonyms":"ZNF411,FLJ90391,BMZF-1","biotype":"protein_coding","ncbi_id":"56242","summary":null,"start":19865886,"end":19894674,"strand":1,"description":"zinc finger protein 253 [Source:HGNC Symbol;Acc:HGNC:13497]"}, {"versioned_ensembl_gene_id":"ENSG00000108788.11","gene_symbol":"MLX","gene_name":"MLX, MAX dimerization protein [Source:HGNC Symbol;Acc:HGNC:11645]","synonyms":"TCFL4,MXD7,MAD7,bHLHd13","biotype":"protein_coding","ncbi_id":"6945","summary":"The product of this gene belongs to the family of basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factors. These factors form heterodimers with Mad proteins and play a role in proliferation, determination and differentiation. This gene product may act to diversify Mad family function by its restricted association with a subset of the Mad family of transcriptional repressors, namely, Mad1 and Mad4. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":42567068,"end":42573239,"strand":1,"description":"MLX, MAX dimerization protein [Source:HGNC Symbol;Acc:HGNC:11645]"}, {"versioned_ensembl_gene_id":"ENSG00000196547.14","gene_symbol":"MAN2A2","gene_name":"mannosidase alpha class 2A member 2 [Source:HGNC Symbol;Acc:HGNC:6825]","synonyms":"MANA2X,HsT19662","biotype":"protein_coding","ncbi_id":"4122","summary":null,"start":90902218,"end":90922584,"strand":1,"description":"mannosidase alpha class 2A member 2 [Source:HGNC Symbol;Acc:HGNC:6825]"}, {"versioned_ensembl_gene_id":"ENSG00000128951.13","gene_symbol":"DUT","gene_name":"deoxyuridine triphosphatase [Source:HGNC Symbol;Acc:HGNC:3078]","synonyms":"dUTPase","biotype":"protein_coding","ncbi_id":"1854","summary":"This gene encodes an essential enzyme of nucleotide metabolism. The encoded protein forms a ubiquitous, homotetrameric enzyme that hydrolyzes dUTP to dUMP and pyrophosphate. This reaction serves two cellular purposes: providing a precursor (dUMP) for the synthesis of thymine nucleotides needed for DNA replication, and limiting intracellular pools of dUTP. Elevated levels of dUTP lead to increased incorporation of uracil into DNA, which induces extensive excision repair mediated by uracil glycosylase. This repair process, resulting in the removal and reincorporation of dUTP, is self-defeating and leads to DNA fragmentation and cell death. Alternative splicing of this gene leads to different isoforms that localize to either the mitochondrion or nucleus. A related pseudogene is located on chromosome 19. [provided by RefSeq, Jul 2008]","start":48331011,"end":48343373,"strand":1,"description":"deoxyuridine triphosphatase [Source:HGNC Symbol;Acc:HGNC:3078]"}, {"versioned_ensembl_gene_id":"ENSG00000226185.2","gene_symbol":"TRIM64FP","gene_name":"tripartite motif containing 64F, pseudogene [Source:HGNC Symbol;Acc:HGNC:43976]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390233","summary":null,"start":95514827,"end":95520107,"strand":1,"description":"tripartite motif containing 64F, pseudogene [Source:HGNC Symbol;Acc:HGNC:43976]"}, {"versioned_ensembl_gene_id":"ENSG00000253789.1","gene_symbol":"NARSP2","gene_name":"asparaginyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50481]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100287895","summary":null,"start":62110524,"end":62119898,"strand":1,"description":"asparaginyl-tRNA synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50481]"}, {"versioned_ensembl_gene_id":"ENSG00000125409.12","gene_symbol":"TEKT3","gene_name":"tektin 3 [Source:HGNC Symbol;Acc:HGNC:14293]","synonyms":"FLJ32828","biotype":"protein_coding","ncbi_id":"64518","summary":"This gene product belongs to the tektin family of proteins. Tektins comprise a family of filament-forming proteins that are coassembled with tubulins to form ciliary and flagellar microtubules. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":15303811,"end":15341641,"strand":-1,"description":"tektin 3 [Source:HGNC Symbol;Acc:HGNC:14293]"}, {"versioned_ensembl_gene_id":"ENSG00000146243.13","gene_symbol":"IRAK1BP1","gene_name":"interleukin 1 receptor associated kinase 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17368]","synonyms":"SIMPL,AIP70","biotype":"protein_coding","ncbi_id":"134728","summary":null,"start":78867472,"end":78946440,"strand":1,"description":"interleukin 1 receptor associated kinase 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17368]"}, {"versioned_ensembl_gene_id":"ENSG00000060688.12","gene_symbol":"SNRNP40","gene_name":"small nuclear ribonucleoprotein U5 subunit 40 [Source:HGNC Symbol;Acc:HGNC:30857]","synonyms":"WDR57,SPF38,PRPF8BP,PRP8BP,HPRP8BP","biotype":"protein_coding","ncbi_id":"9410","summary":"This gene encodes a component of the U5 small nuclear ribonucleoprotein (snRNP) particle. The U5 snRNP is part of the spliceosome, a multiprotein complex that catalyzes the removal of introns from pre-messenger RNAs. [provided by RefSeq, Jul 2008]","start":31259568,"end":31296782,"strand":-1,"description":"small nuclear ribonucleoprotein U5 subunit 40 [Source:HGNC Symbol;Acc:HGNC:30857]"}, {"versioned_ensembl_gene_id":"ENSG00000234456.7","gene_symbol":"MAGI2-AS3","gene_name":"MAGI2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40862]","synonyms":"ENST00000414797","biotype":"processed_transcript","ncbi_id":"100505881","summary":null,"start":79452877,"end":79471208,"strand":1,"description":"MAGI2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40862]"}, {"versioned_ensembl_gene_id":"ENSG00000217512.1","gene_symbol":"AL356776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79067692,"end":79068138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141161.11","gene_symbol":"UNC45B","gene_name":"unc-45 myosin chaperone B [Source:HGNC Symbol;Acc:HGNC:14304]","synonyms":"UNC45,CMYA4","biotype":"protein_coding","ncbi_id":"146862","summary":"This gene encodes a co-chaperone required for folding and accumulation of type II myosins. The protein consists of three tetratricopeptide repeat motifs at the N-terminus that form a complex with heat shock protein 90, a central region of unknown function that is conserved in all Unc-45 proteins, and a C-terminal Unc-45/Cro1/She4 domain. The protein is expressed at high levels in striated muscle, where its muscle myosin chaperone activity is dependent on heat shock protein 90 acting as a co-chaperone. A missense mutation in this gene has been associated with cataract development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":35147817,"end":35189345,"strand":1,"description":"unc-45 myosin chaperone B [Source:HGNC Symbol;Acc:HGNC:14304]"}, {"versioned_ensembl_gene_id":"ENSG00000185069.2","gene_symbol":"KRT76","gene_name":"keratin 76 [Source:HGNC Symbol;Acc:HGNC:24430]","synonyms":"KRT2P,KRT2B,HUMCYT2A","biotype":"protein_coding","ncbi_id":"51350","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. The type II keratins are clustered in a region of chromosome 12q13. [provided by RefSeq, Jun 2009]","start":52768155,"end":52777345,"strand":-1,"description":"keratin 76 [Source:HGNC Symbol;Acc:HGNC:24430]"}, {"versioned_ensembl_gene_id":"ENSG00000227834.1","gene_symbol":"AP003385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67651576,"end":67653404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108506.11","gene_symbol":"INTS2","gene_name":"integrator complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:29241]","synonyms":"KIAA1287,INT2","biotype":"protein_coding","ncbi_id":"57508","summary":"INTS2 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":61865367,"end":61928016,"strand":-1,"description":"integrator complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:29241]"}, {"versioned_ensembl_gene_id":"ENSG00000104879.4","gene_symbol":"CKM","gene_name":"creatine kinase, M-type [Source:HGNC Symbol;Acc:HGNC:1994]","synonyms":"CKMM","biotype":"protein_coding","ncbi_id":"1158","summary":"The protein encoded by this gene is a cytoplasmic enzyme involved in energy homeostasis and is an important serum marker for myocardial infarction. The encoded protein reversibly catalyzes the transfer of phosphate between ATP and various phosphogens such as creatine phosphate. It acts as a homodimer in striated muscle as well as in other tissues, and as a heterodimer with a similar brain isozyme in heart. The encoded protein is a member of the ATP:guanido phosphotransferase protein family. [provided by RefSeq, Jul 2008]","start":45306414,"end":45322977,"strand":-1,"description":"creatine kinase, M-type [Source:HGNC Symbol;Acc:HGNC:1994]"}, {"versioned_ensembl_gene_id":"ENSG00000188656.8","gene_symbol":"TSPY7P","gene_name":"testis specific protein, Y-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:34040]","synonyms":"TSPYP7","biotype":"unprocessed_pseudogene","ncbi_id":"653288","summary":null,"start":9378122,"end":9380871,"strand":1,"description":"testis specific protein, Y-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:34040]"}, {"versioned_ensembl_gene_id":"ENSG00000276693.1","gene_symbol":"AC138466.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132169823,"end":132170043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230124.6","gene_symbol":"ACBD6","gene_name":"acyl-CoA binding domain containing 6 [Source:HGNC Symbol;Acc:HGNC:23339]","synonyms":"MGC2404","biotype":"protein_coding","ncbi_id":"84320","summary":null,"start":180269653,"end":180502954,"strand":-1,"description":"acyl-CoA binding domain containing 6 [Source:HGNC Symbol;Acc:HGNC:23339]"}, {"versioned_ensembl_gene_id":"ENSG00000255203.1","gene_symbol":"OR7E2P","gene_name":"olfactory receptor family 7 subfamily E member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8402]","synonyms":"OR7F2P,OR7E51P,OR11-6,hg94","biotype":"unprocessed_pseudogene","ncbi_id":"8587","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":86857059,"end":86857947,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8402]"}, {"versioned_ensembl_gene_id":"ENSG00000186481.16","gene_symbol":"ANKRD20A5P","gene_name":"ankyrin repeat domain 20 family member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:33833]","synonyms":"MGC26718,ANKRD20A5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440482","summary":null,"start":14179097,"end":14252140,"strand":1,"description":"ankyrin repeat domain 20 family member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:33833]"}, {"versioned_ensembl_gene_id":"ENSG00000264546.1","gene_symbol":"AC008026.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":62549726,"end":62552121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266145.1","gene_symbol":"AP001004.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14222008,"end":14222331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249426.1","gene_symbol":"AC093206.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118760474,"end":118785459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214878.2","gene_symbol":"RPL5P31","gene_name":"ribosomal protein L5 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42036]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341674","summary":null,"start":51161723,"end":51162357,"strand":-1,"description":"ribosomal protein L5 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42036]"}, {"versioned_ensembl_gene_id":"ENSG00000230561.4","gene_symbol":"CCDC192","gene_name":"coiled-coil domain containing 192 [Source:HGNC Symbol;Acc:HGNC:49566]","synonyms":"LINC01183","biotype":"protein_coding","ncbi_id":"728586","summary":null,"start":127703389,"end":127941634,"strand":1,"description":"coiled-coil domain containing 192 [Source:HGNC Symbol;Acc:HGNC:49566]"}, {"versioned_ensembl_gene_id":"ENSG00000249797.1","gene_symbol":"LINC02147","gene_name":"long intergenic non-protein coding RNA 2147 [Source:HGNC Symbol;Acc:HGNC:53007]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467224","summary":null,"start":117925008,"end":118266035,"strand":1,"description":"long intergenic non-protein coding RNA 2147 [Source:HGNC Symbol;Acc:HGNC:53007]"}, {"versioned_ensembl_gene_id":"ENSG00000240889.1","gene_symbol":"NDUFB2-AS1","gene_name":"NDUFB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40396]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100134713","summary":null,"start":140695336,"end":140697077,"strand":-1,"description":"NDUFB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40396]"}, {"versioned_ensembl_gene_id":"ENSG00000274019.1","gene_symbol":"AC239804.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149111304,"end":149121866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264148.1","gene_symbol":"AC138207.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31008154,"end":31008319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251090.2","gene_symbol":"OR5AC4P","gene_name":"olfactory receptor family 5 subfamily AC member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31284]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"403271","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98100793,"end":98105672,"strand":1,"description":"olfactory receptor family 5 subfamily AC member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:31284]"}, {"versioned_ensembl_gene_id":"ENSG00000260082.1","gene_symbol":"AC106886.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30821068,"end":30822110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239670.1","gene_symbol":"AL355864.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32986952,"end":32988233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270091.1","gene_symbol":"AC015726.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19896590,"end":19897287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276064.1","gene_symbol":"AL365222.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77343557,"end":77343654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255560.1","gene_symbol":"OR4R2P","gene_name":"olfactory receptor family 4 subfamily R member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15181]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81299","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54657120,"end":54657716,"strand":-1,"description":"olfactory receptor family 4 subfamily R member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15181]"}, {"versioned_ensembl_gene_id":"ENSG00000217644.5","gene_symbol":"AL355864.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32979947,"end":32980472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244274.7","gene_symbol":"DBNDD2","gene_name":"dysbindin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15881]","synonyms":"HSMNP1,C20orf35","biotype":"protein_coding","ncbi_id":"55861","summary":null,"start":45406057,"end":45410610,"strand":1,"description":"dysbindin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15881]"}, {"versioned_ensembl_gene_id":"ENSG00000280594.1","gene_symbol":"BTG3-AS1","gene_name":"BTG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53145]","synonyms":"ASBEL","biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":17611744,"end":17633199,"strand":1,"description":"BTG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53145]"}, {"versioned_ensembl_gene_id":"ENSG00000233824.1","gene_symbol":"AC003985.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25321302,"end":25326815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105954.2","gene_symbol":"NPVF","gene_name":"neuropeptide VF precursor [Source:HGNC Symbol;Acc:HGNC:13782]","synonyms":"RFRP,C7orf9","biotype":"protein_coding","ncbi_id":"64111","summary":null,"start":25224570,"end":25228486,"strand":-1,"description":"neuropeptide VF precursor [Source:HGNC Symbol;Acc:HGNC:13782]"}, {"versioned_ensembl_gene_id":"ENSG00000267650.1","gene_symbol":"AC008742.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9995997,"end":9997163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280953.2","gene_symbol":"LINC01163","gene_name":"long intergenic non-protein coding RNA 1163 [Source:NCBI gene;Acc:101927381]","synonyms":"TCONS_00017722","biotype":"lincRNA","ncbi_id":"101927381","summary":null,"start":128181032,"end":128317726,"strand":1,"description":"long intergenic non-protein coding RNA 1163 [Source:NCBI gene;Acc:101927381]"}, {"versioned_ensembl_gene_id":"ENSG00000263624.1","gene_symbol":"AC055811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17167946,"end":17185554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257343.1","gene_symbol":"AC055716.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52746596,"end":52748308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119688.20","gene_symbol":"ABCD4","gene_name":"ATP binding cassette subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:68]","synonyms":"PXMP1L,PMP69,P70R,EST352188","biotype":"protein_coding","ncbi_id":"5826","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown. However, it is speculated that it may function as a heterodimer for another peroxisomal ABC transporter and, therefore, may modify the adrenoleukodystrophy phenotype. It may also play a role in the process of peroxisome biogenesis. Alternative splicing results in several protein-coding and non-protein-coding variants. [provided by RefSeq, Jul 2017]","start":74285423,"end":74303056,"strand":-1,"description":"ATP binding cassette subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:68]"}, {"versioned_ensembl_gene_id":"ENSG00000185681.12","gene_symbol":"MORN5","gene_name":"MORN repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:17841]","synonyms":"FLJ46909,C9orf18,C9orf113","biotype":"protein_coding","ncbi_id":"254956","summary":null,"start":122159908,"end":122200088,"strand":1,"description":"MORN repeat containing 5 [Source:HGNC Symbol;Acc:HGNC:17841]"}, {"versioned_ensembl_gene_id":"ENSG00000168530.15","gene_symbol":"MYL1","gene_name":"myosin light chain 1 [Source:HGNC Symbol;Acc:HGNC:7582]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4632","summary":"Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in fast skeletal muscle. Two transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]","start":210290150,"end":210315190,"strand":-1,"description":"myosin light chain 1 [Source:HGNC Symbol;Acc:HGNC:7582]"}, {"versioned_ensembl_gene_id":"ENSG00000278561.1","gene_symbol":"PTPN20CP","gene_name":"protein tyrosine phosphatase, non-receptor type 20C, pseudogene [Source:HGNC Symbol;Acc:HGNC:23424]","synonyms":"PTPN20C,bA164N7.3","biotype":"unprocessed_pseudogene","ncbi_id":"653045","summary":null,"start":48064308,"end":48119455,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 20C, pseudogene [Source:HGNC Symbol;Acc:HGNC:23424]"}, {"versioned_ensembl_gene_id":"ENSG00000120437.8","gene_symbol":"ACAT2","gene_name":"acetyl-CoA acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:94]","synonyms":null,"biotype":"protein_coding","ncbi_id":"39","summary":"The product of this gene is an enzyme involved in lipid metabolism, and it encodes cytosolic acetoacetyl-CoA thiolase. This gene shows complementary overlapping with the 3-prime region of the TCP1 gene in both mouse and human. These genes are encoded on opposite strands of DNA, as well as in opposite transcriptional orientation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":159760328,"end":159779055,"strand":1,"description":"acetyl-CoA acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:94]"}, {"versioned_ensembl_gene_id":"ENSG00000221826.9","gene_symbol":"PSG3","gene_name":"pregnancy specific beta-1-glycoprotein 3 [Source:HGNC Symbol;Acc:HGNC:9520]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5671","summary":"The human pregnancy-specific glycoproteins (PSGs) are a family of proteins that are synthesized in large amounts by placental trophoblasts and released into the maternal circulation during pregnancy. Molecular cloning and analysis of several PSG genes has indicated that the PSGs form a subgroup of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily of genes. Members of the CEA family consist of a single N domain, with structural similarity to the immunoglobulin variable domains, followed by a variable number of immunoglobulin constant-like A and/or B domains. Most PSGs have an arg-gly-asp (RGD) motif, which has been shown to function as an adhesion recognition signal for several integrins, in the N-terminal domain (summary by Teglund et al., 1994 [PubMed 7851896]). For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]","start":42721638,"end":42740569,"strand":-1,"description":"pregnancy specific beta-1-glycoprotein 3 [Source:HGNC Symbol;Acc:HGNC:9520]"}, {"versioned_ensembl_gene_id":"ENSG00000263887.6","gene_symbol":"AC053481.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62282387,"end":62297026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266971.1","gene_symbol":"OR4F8P","gene_name":"olfactory receptor family 4 subfamily F member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15395]","synonyms":"OR4F9P,OR4F20P","biotype":"unprocessed_pseudogene","ncbi_id":"390872","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":156279,"end":157215,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15395]"}, {"versioned_ensembl_gene_id":"ENSG00000267792.1","gene_symbol":"WBP1LP11","gene_name":"WW domain binding protein 1-like pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51471]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481969","summary":null,"start":145485,"end":145812,"strand":1,"description":"WW domain binding protein 1-like pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51471]"}, {"versioned_ensembl_gene_id":"ENSG00000249150.1","gene_symbol":"AC010267.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116820993,"end":116830187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145920.14","gene_symbol":"CPLX2","gene_name":"complexin 2 [Source:HGNC Symbol;Acc:HGNC:2310]","synonyms":"DKFZp547D155,CPX-2","biotype":"protein_coding","ncbi_id":"10814","summary":"Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the SNAP receptor complex and disrupts it, allowing transmitter release. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":175796310,"end":175884020,"strand":1,"description":"complexin 2 [Source:HGNC Symbol;Acc:HGNC:2310]"}, {"versioned_ensembl_gene_id":"ENSG00000225879.1","gene_symbol":"AL109924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168962610,"end":168964341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170619.9","gene_symbol":"COMMD5","gene_name":"COMM domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17902]","synonyms":"HT002,HCaRG,FLJ13008","biotype":"protein_coding","ncbi_id":"28991","summary":null,"start":144841042,"end":144853736,"strand":-1,"description":"COMM domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17902]"}, {"versioned_ensembl_gene_id":"ENSG00000179743.4","gene_symbol":"FLJ37453","gene_name":"uncharacterized LOC729614 [Source:NCBI gene;Acc:729614]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729614","summary":null,"start":15834474,"end":15848147,"strand":-1,"description":"uncharacterized LOC729614 [Source:NCBI gene;Acc:729614]"}, {"versioned_ensembl_gene_id":"ENSG00000269584.1","gene_symbol":"TDGF1P7","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:11707]","synonyms":"TDGF7,CRIPTO-7,CR-7","biotype":"processed_pseudogene","ncbi_id":"100129080","summary":null,"start":39534463,"end":39535021,"strand":1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:11707]"}, {"versioned_ensembl_gene_id":"ENSG00000143595.12","gene_symbol":"AQP10","gene_name":"aquaporin 10 [Source:HGNC Symbol;Acc:HGNC:16029]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89872","summary":"This gene encodes a member of the aquaglyceroporin family of integral membrane proteins. Members of this family function as water-permeable channels in the epithelia of organs that absorb and excrete water. This protein was shown to function as a water-selective channel, and could also permeate neutral solutes such as glycerol and urea. [provided by RefSeq, Jul 2008]","start":154321090,"end":154325325,"strand":1,"description":"aquaporin 10 [Source:HGNC Symbol;Acc:HGNC:16029]"}, {"versioned_ensembl_gene_id":"ENSG00000255815.3","gene_symbol":"KRT8P11","gene_name":"keratin 8 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:31058]","synonyms":"RP11-13B9.3,KRT8L1","biotype":"processed_pseudogene","ncbi_id":"347265","summary":null,"start":99305176,"end":99306611,"strand":1,"description":"keratin 8 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:31058]"}, {"versioned_ensembl_gene_id":"ENSG00000271232.1","gene_symbol":"CARSP1","gene_name":"cysteinyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50477]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420042","summary":null,"start":68749501,"end":68750691,"strand":1,"description":"cysteinyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50477]"}, {"versioned_ensembl_gene_id":"ENSG00000170759.10","gene_symbol":"KIF5B","gene_name":"kinesin family member 5B [Source:HGNC Symbol;Acc:HGNC:6324]","synonyms":"KNS1,KNS","biotype":"protein_coding","ncbi_id":"3799","summary":null,"start":32009010,"end":32056431,"strand":-1,"description":"kinesin family member 5B [Source:HGNC Symbol;Acc:HGNC:6324]"}, {"versioned_ensembl_gene_id":"ENSG00000232153.2","gene_symbol":"AC073218.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34734975,"end":34737118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204754.3","gene_symbol":"LINC01951","gene_name":"long intergenic non-protein coding RNA 1951 [Source:HGNC Symbol;Acc:HGNC:52774]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441116","summary":null,"start":174919082,"end":174995513,"strand":-1,"description":"long intergenic non-protein coding RNA 1951 [Source:HGNC Symbol;Acc:HGNC:52774]"}, {"versioned_ensembl_gene_id":"ENSG00000156500.14","gene_symbol":"FAM122C","gene_name":"family with sequence similarity 122C [Source:HGNC Symbol;Acc:HGNC:25202]","synonyms":"RP3-473B4.1","biotype":"protein_coding","ncbi_id":"159091","summary":null,"start":134796789,"end":134854610,"strand":1,"description":"family with sequence similarity 122C [Source:HGNC Symbol;Acc:HGNC:25202]"}, {"versioned_ensembl_gene_id":"ENSG00000251670.1","gene_symbol":"AC113346.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174751304,"end":174850725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143633.12","gene_symbol":"C1orf131","gene_name":"chromosome 1 open reading frame 131 [Source:HGNC Symbol;Acc:HGNC:25332]","synonyms":"DKFZp547B1713","biotype":"protein_coding","ncbi_id":"128061","summary":null,"start":231223763,"end":231241187,"strand":-1,"description":"chromosome 1 open reading frame 131 [Source:HGNC Symbol;Acc:HGNC:25332]"}, {"versioned_ensembl_gene_id":"ENSG00000164253.13","gene_symbol":"WDR41","gene_name":"WD repeat domain 41 [Source:HGNC Symbol;Acc:HGNC:25601]","synonyms":"FLJ10904","biotype":"protein_coding","ncbi_id":"55255","summary":null,"start":77425970,"end":77620611,"strand":-1,"description":"WD repeat domain 41 [Source:HGNC Symbol;Acc:HGNC:25601]"}, {"versioned_ensembl_gene_id":"ENSG00000249970.1","gene_symbol":"AC074250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73543822,"end":73544013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280286.1","gene_symbol":"FRG1KP","gene_name":"FSHD region gene 1 family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:51769]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102724923","summary":null,"start":65646982,"end":65652679,"strand":-1,"description":"FSHD region gene 1 family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:51769]"}, {"versioned_ensembl_gene_id":"ENSG00000234091.1","gene_symbol":"AL157392.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13729383,"end":13756200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146192.14","gene_symbol":"FGD2","gene_name":"FYVE, RhoGEF and PH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:3664]","synonyms":"ZFYVE4","biotype":"protein_coding","ncbi_id":"221472","summary":"The protein encoded by this gene belongs to a family of guanine nucleotide exchange factors (GEFs) which control cytoskeleton-dependent membrane rearrangements by activating the cell division cycle 42 (CDC42) protein. This gene is expressed in B lymphocytes, macrophages, and dendritic cells. The encoded protein may play a role in leukocyte signaling and vesicle trafficking in antigen-presenting cells in the immune system. [provided by RefSeq, Oct 2016]","start":37005646,"end":37029070,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:3664]"}, {"versioned_ensembl_gene_id":"ENSG00000278299.5","gene_symbol":"TBC1D3C","gene_name":"TBC1 domain family member 3C [Source:HGNC Symbol;Acc:HGNC:24889]","synonyms":"MGC44903","biotype":"protein_coding","ncbi_id":"414060","summary":"This gene represents one of a cluster of related genes found on chromosome 17. The proteins encoded by this gene family contain a TBC (Tre-2, Bub2p, and Cdc16p) domain and may be involved in GTPase signaling and vesicle trafficking. [provided by RefSeq, Apr 2014]","start":38057693,"end":38068592,"strand":-1,"description":"TBC1 domain family member 3C [Source:HGNC Symbol;Acc:HGNC:24889]"}, {"versioned_ensembl_gene_id":"ENSG00000012504.13","gene_symbol":"NR1H4","gene_name":"nuclear receptor subfamily 1 group H member 4 [Source:HGNC Symbol;Acc:HGNC:7967]","synonyms":"RIP14,HRR1,HRR-1,FXR","biotype":"protein_coding","ncbi_id":"9971","summary":"This gene encodes a ligand-activated transcription factor that shares structural features in common with nuclear hormone receptor family members. This protein functions as a receptor for bile acids, and when bound to bile acids, binds to DNA and regulates the expression of genes involved in bile acid synthesis and transport. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Feb 2016]","start":100473708,"end":100564413,"strand":1,"description":"nuclear receptor subfamily 1 group H member 4 [Source:HGNC Symbol;Acc:HGNC:7967]"}, {"versioned_ensembl_gene_id":"ENSG00000133808.4","gene_symbol":"MICALCL","gene_name":"MICAL C-terminal like [Source:HGNC Symbol;Acc:HGNC:25933]","synonyms":"FLJ14966","biotype":"protein_coding","ncbi_id":"84953","summary":null,"start":12276080,"end":12359144,"strand":1,"description":"MICAL C-terminal like [Source:HGNC Symbol;Acc:HGNC:25933]"}, {"versioned_ensembl_gene_id":"ENSG00000145832.12","gene_symbol":"SLC25A48","gene_name":"solute carrier family 25 member 48 [Source:HGNC Symbol;Acc:HGNC:30451]","synonyms":"HDMCP,FLJ44862","biotype":"protein_coding","ncbi_id":"153328","summary":null,"start":135834649,"end":135888637,"strand":1,"description":"solute carrier family 25 member 48 [Source:HGNC Symbol;Acc:HGNC:30451]"}, {"versioned_ensembl_gene_id":"ENSG00000121289.17","gene_symbol":"CEP89","gene_name":"centrosomal protein 89 [Source:HGNC Symbol;Acc:HGNC:25907]","synonyms":"FLJ14640,CCDC123","biotype":"protein_coding","ncbi_id":"84902","summary":null,"start":32875925,"end":32971991,"strand":-1,"description":"centrosomal protein 89 [Source:HGNC Symbol;Acc:HGNC:25907]"}, {"versioned_ensembl_gene_id":"ENSG00000223749.9","gene_symbol":"MIR503HG","gene_name":"MIR503 host gene [Source:HGNC Symbol;Acc:HGNC:28258]","synonyms":"MGC16121,H19X","biotype":"lincRNA","ncbi_id":"84848","summary":null,"start":134543337,"end":134546632,"strand":-1,"description":"MIR503 host gene [Source:HGNC Symbol;Acc:HGNC:28258]"}, {"versioned_ensembl_gene_id":"ENSG00000246763.6","gene_symbol":"RGMB-AS1","gene_name":"RGMB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48666]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"503569","summary":null,"start":98769618,"end":98773469,"strand":-1,"description":"RGMB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48666]"}, {"versioned_ensembl_gene_id":"ENSG00000164039.14","gene_symbol":"BDH2","gene_name":"3-hydroxybutyrate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:32389]","synonyms":"UNQ6308,UCPA-OR,SDR15C1,PRO20933,FLJ13261,DHRS6","biotype":"protein_coding","ncbi_id":"56898","summary":null,"start":103079435,"end":103099883,"strand":-1,"description":"3-hydroxybutyrate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:32389]"}, {"versioned_ensembl_gene_id":"ENSG00000083807.9","gene_symbol":"SLC27A5","gene_name":"solute carrier family 27 member 5 [Source:HGNC Symbol;Acc:HGNC:10999]","synonyms":"VLCSH2,VLCS-H2,FLJ22987,VLACSR,FATP5,FACVL3,ACSVL6,ACSB","biotype":"protein_coding","ncbi_id":"10998","summary":"The protein encoded by this gene is an isozyme of very long-chain acyl-CoA synthetase (VLCS). It is capable of activating very long-chain fatty-acids containing 24- and 26-carbons. It is expressed in liver and associated with endoplasmic reticulum but not with peroxisomes. Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation. This gene has a mouse ortholog. [provided by RefSeq, Jul 2008]","start":58479512,"end":58512413,"strand":-1,"description":"solute carrier family 27 member 5 [Source:HGNC Symbol;Acc:HGNC:10999]"}, {"versioned_ensembl_gene_id":"ENSG00000036549.12","gene_symbol":"ZZZ3","gene_name":"zinc finger ZZ-type containing 3 [Source:HGNC Symbol;Acc:HGNC:24523]","synonyms":"DKFZP564I052,ATAC1","biotype":"protein_coding","ncbi_id":"26009","summary":null,"start":77562416,"end":77683419,"strand":-1,"description":"zinc finger ZZ-type containing 3 [Source:HGNC Symbol;Acc:HGNC:24523]"}, {"versioned_ensembl_gene_id":"ENSG00000167508.11","gene_symbol":"MVD","gene_name":"mevalonate diphosphate decarboxylase [Source:HGNC Symbol;Acc:HGNC:7529]","synonyms":"MPD","biotype":"protein_coding","ncbi_id":"4597","summary":"The enzyme mevalonate pyrophosphate decarboxylase catalyzes the conversion of mevalonate pyrophosphate into isopentenyl pyrophosphate in one of the early steps in cholesterol biosynthesis. It decarboxylates and dehydrates its substrate while hydrolyzing ATP. [provided by RefSeq, Jul 2008]","start":88651935,"end":88663161,"strand":-1,"description":"mevalonate diphosphate decarboxylase [Source:HGNC Symbol;Acc:HGNC:7529]"}, {"versioned_ensembl_gene_id":"ENSG00000273093.1","gene_symbol":"AC097065.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":200315435,"end":200315967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116337.15","gene_symbol":"AMPD2","gene_name":"adenosine monophosphate deaminase 2 [Source:HGNC Symbol;Acc:HGNC:469]","synonyms":"SPG63","biotype":"protein_coding","ncbi_id":"271","summary":"The protein encoded by this gene is important in purine metabolism by converting AMP to IMP. The encoded protein, which acts as a homotetramer, is one of three AMP deaminases found in mammals. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":109616104,"end":109632051,"strand":1,"description":"adenosine monophosphate deaminase 2 [Source:HGNC Symbol;Acc:HGNC:469]"}, {"versioned_ensembl_gene_id":"ENSG00000250420.8","gene_symbol":"AACSP1","gene_name":"acetoacetyl-CoA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18226]","synonyms":"AACSL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729522","summary":null,"start":178764861,"end":178818435,"strand":-1,"description":"acetoacetyl-CoA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18226]"}, {"versioned_ensembl_gene_id":"ENSG00000163466.15","gene_symbol":"ARPC2","gene_name":"actin related protein 2/3 complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:705]","synonyms":"p34-Arc,ARC34","biotype":"protein_coding","ncbi_id":"10109","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p34 subunit, has yet to be determined. Two alternatively spliced variants have been characterized to date. Additional alternatively spliced variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":218217094,"end":218254356,"strand":1,"description":"actin related protein 2/3 complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:705]"}, {"versioned_ensembl_gene_id":"ENSG00000121905.9","gene_symbol":"HPCA","gene_name":"hippocalcin [Source:HGNC Symbol;Acc:HGNC:5144]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3208","summary":"The protein encoded by this gene is a member of neuron-specific calcium-binding proteins family found in the retina and brain. This protein is associated with the plasma membrane. It has similarities to proteins located in the photoreceptor cells that regulate photosignal transduction in a calcium-sensitive manner. This protein displays recoverin activity and a calcium-dependent inhibition of rhodopsin kinase. It is identical to the rat and mouse hippocalcin proteins and thought to play an important role in neurons of the central nervous system in a number of species. [provided by RefSeq, Jul 2008]","start":32885994,"end":32898441,"strand":1,"description":"hippocalcin [Source:HGNC Symbol;Acc:HGNC:5144]"}, {"versioned_ensembl_gene_id":"ENSG00000135253.13","gene_symbol":"KCP","gene_name":"kielin/chordin-like protein [Source:HGNC Symbol;Acc:HGNC:17585]","synonyms":"NET67,FLJ33365,CRIM2","biotype":"protein_coding","ncbi_id":"375616","summary":null,"start":128862451,"end":128910719,"strand":-1,"description":"kielin/chordin-like protein [Source:HGNC Symbol;Acc:HGNC:17585]"}, {"versioned_ensembl_gene_id":"ENSG00000124177.14","gene_symbol":"CHD6","gene_name":"chromodomain helicase DNA binding protein 6 [Source:HGNC Symbol;Acc:HGNC:19057]","synonyms":"RIGB,KIAA1335,FLJ22369,dJ620E11.1,CHD5","biotype":"protein_coding","ncbi_id":"84181","summary":"This gene encodes a member of the SNF2/RAD54 helicase protein family. The encoded protein contains two chromodomains, a helicase domain, and an ATPase domain. Several multi-subunit protein complexes remodel chromatin to allow patterns of cell type-specific gene expression, and the encoded protein is thought to be a core member of one or more of these chromatin remodeling complexes. The encoded protein may function as a transcriptional repressor and is involved in the cellular repression of influenza virus replication. [provided by RefSeq, Jul 2013]","start":41402101,"end":41618494,"strand":-1,"description":"chromodomain helicase DNA binding protein 6 [Source:HGNC Symbol;Acc:HGNC:19057]"}, {"versioned_ensembl_gene_id":"ENSG00000219146.1","gene_symbol":"RPS4XP8","gene_name":"ribosomal protein S4X pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36683]","synonyms":"RPS4P8","biotype":"processed_pseudogene","ncbi_id":"646269","summary":null,"start":154576309,"end":154577079,"strand":1,"description":"ribosomal protein S4X pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36683]"}, {"versioned_ensembl_gene_id":"ENSG00000213904.8","gene_symbol":"LIPE-AS1","gene_name":"LIPE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48589]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996307","summary":null,"start":42397128,"end":42652355,"strand":1,"description":"LIPE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48589]"}, {"versioned_ensembl_gene_id":"ENSG00000226268.3","gene_symbol":"AC135977.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49433480,"end":49434438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123447.6","gene_symbol":"TYRL","gene_name":"tyrosinase-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12443]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"7300","summary":null,"start":49405091,"end":49415789,"strand":-1,"description":"tyrosinase-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12443]"}, {"versioned_ensembl_gene_id":"ENSG00000167656.4","gene_symbol":"LY6D","gene_name":"lymphocyte antigen 6 family member D [Source:HGNC Symbol;Acc:HGNC:13348]","synonyms":"E48","biotype":"protein_coding","ncbi_id":"8581","summary":null,"start":142784880,"end":142786592,"strand":-1,"description":"lymphocyte antigen 6 family member D [Source:HGNC Symbol;Acc:HGNC:13348]"}, {"versioned_ensembl_gene_id":"ENSG00000183044.11","gene_symbol":"ABAT","gene_name":"4-aminobutyrate aminotransferase [Source:HGNC Symbol;Acc:HGNC:23]","synonyms":"GABAT","biotype":"protein_coding","ncbi_id":"18","summary":"4-aminobutyrate aminotransferase (ABAT) is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. The active enzyme is a homodimer of 50-kD subunits complexed to pyridoxal-5-phosphate. The protein sequence is over 95% similar to the pig protein. GABA is estimated to be present in nearly one-third of human synapses. ABAT in liver and brain is controlled by 2 codominant alleles with a frequency in a Caucasian population of 0.56 and 0.44. The ABAT deficiency phenotype includes psychomotor retardation, hypotonia, hyperreflexia, lethargy, refractory seizures, and EEG abnormalities. Multiple alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":8674565,"end":8784575,"strand":1,"description":"4-aminobutyrate aminotransferase [Source:HGNC Symbol;Acc:HGNC:23]"}, {"versioned_ensembl_gene_id":"ENSG00000233091.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30687065,"end":30687794,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000197114.11","gene_symbol":"ZGPAT","gene_name":"zinc finger CCCH-type and G-patch domain containing [Source:HGNC Symbol;Acc:HGNC:15948]","synonyms":"MGC44880,KIAA1847,GPATCH6,GPATC6,FLJ14972,dJ583P15.3,ZIP,ZC3HDC9,ZC3H9","biotype":"protein_coding","ncbi_id":"84619","summary":null,"start":63707465,"end":63736142,"strand":1,"description":"zinc finger CCCH-type and G-patch domain containing [Source:HGNC Symbol;Acc:HGNC:15948]"}, {"versioned_ensembl_gene_id":"ENSG00000235394.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":29996148,"end":30056801,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000172425.10","gene_symbol":"TTC36","gene_name":"tetratricopeptide repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:33708]","synonyms":"HBP21","biotype":"protein_coding","ncbi_id":"143941","summary":"The protein encoded by this gene has three tetratricopeptide repeats and is a chaperone for heat shock protein 70. The encoded protein may function as a tumor suppressor in hepatocellular carcinoma (HCC) since it promotes apoptosis but is downregulated in HCC. [provided by RefSeq, Sep 2016]","start":118527472,"end":118531197,"strand":1,"description":"tetratricopeptide repeat domain 36 [Source:HGNC Symbol;Acc:HGNC:33708]"}, {"versioned_ensembl_gene_id":"ENSG00000131389.16","gene_symbol":"SLC6A6","gene_name":"solute carrier family 6 member 6 [Source:HGNC Symbol;Acc:HGNC:11052]","synonyms":"TAUT","biotype":"protein_coding","ncbi_id":"6533","summary":"This gene encodes a multi-pass membrane protein that is a member of a family of sodium and chloride-ion dependent transporters. The encoded protein transports taurine and beta-alanine. There is a pseudogene for this gene on chromosome 21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":14402576,"end":14489349,"strand":1,"description":"solute carrier family 6 member 6 [Source:HGNC Symbol;Acc:HGNC:11052]"}, {"versioned_ensembl_gene_id":"ENSG00000231745.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29989570,"end":29990447,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000214145.6","gene_symbol":"LINC00887","gene_name":"long intergenic non-protein coding RNA 887 [Source:HGNC Symbol;Acc:HGNC:48574]","synonyms":"linc-ATP13A4-8,HEIRCC","biotype":"lincRNA","ncbi_id":"100131551","summary":null,"start":194296465,"end":194312803,"strand":-1,"description":"long intergenic non-protein coding RNA 887 [Source:HGNC Symbol;Acc:HGNC:48574]"}, {"versioned_ensembl_gene_id":"ENSG00000265485.5","gene_symbol":"LINC01915","gene_name":"long intergenic non-protein coding RNA 1915 [Source:HGNC Symbol;Acc:HGNC:52734]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729950","summary":null,"start":24628182,"end":24662198,"strand":1,"description":"long intergenic non-protein coding RNA 1915 [Source:HGNC Symbol;Acc:HGNC:52734]"}, {"versioned_ensembl_gene_id":"ENSG00000278181.1","gene_symbol":"AP000457.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17296219,"end":17296596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281937.1","gene_symbol":"Z98044.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9197143,"end":9198906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282657.3","gene_symbol":"IGHM","gene_name":"immunoglobulin heavy constant mu [Source:HGNC Symbol;Acc:HGNC:5541]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3507","summary":"Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains and 2 identical light chains (see MIM 147200) joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. Each Ig heavy chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by an individual C region gene, that determines the isotype of the antibody and provides effector or signaling functions. The heavy chain V region is encoded by 1 each of 3 types of genes: V genes (see MIM 147070), joining (J) genes (see MIM 147010), and diversity (D) genes (see MIM 146910). The C region genes are clustered downstream of the V region genes within the heavy chain locus on chromosome 14. The IGHM gene encodes the C region of the mu heavy chain, which defines the IgM isotype. Naive B cells express the transmembrane forms of IgM and IgD (see IGHD; MIM 1471770) on their surface. During an antibody response, activated B cells can switch to the expression of individual downstream heavy chain C region genes by a process of somatic recombination known as isotype switching. In addition, secreted Ig forms that act as antibodies can be produced by alternative RNA processing of the heavy chain C region sequences. Although the membrane forms of all Ig isotypes are monomeric, secreted IgM forms pentamers, and occasionally hexamers, in plasma (summary by Janeway et al., 2005).[supplied by OMIM, Aug 2010]","start":105854991,"end":105856989,"strand":-1,"description":"immunoglobulin heavy constant mu [Source:HGNC Symbol;Acc:HGNC:5541]"}, {"versioned_ensembl_gene_id":"ENSG00000134461.15","gene_symbol":"ANKRD16","gene_name":"ankyrin repeat domain 16 [Source:HGNC Symbol;Acc:HGNC:23471]","synonyms":"DKFZP434N1511","biotype":"protein_coding","ncbi_id":"54522","summary":null,"start":5861617,"end":5889906,"strand":-1,"description":"ankyrin repeat domain 16 [Source:HGNC Symbol;Acc:HGNC:23471]"}, {"versioned_ensembl_gene_id":"ENSG00000231718.1","gene_symbol":"AC099673.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":199148598,"end":199393307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000019549.9","gene_symbol":"SNAI2","gene_name":"snail family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:11094]","synonyms":"SNAIL2,SLUGH1,SLUGH,SLUG","biotype":"protein_coding","ncbi_id":"6591","summary":"This gene encodes a member of the Snail family of C2H2-type zinc finger transcription factors. The encoded protein acts as a transcriptional repressor that binds to E-box motifs and is also likely to repress E-cadherin transcription in breast carcinoma. This protein is involved in epithelial-mesenchymal transitions and has antiapoptotic activity. Mutations in this gene may be associated with sporatic cases of neural tube defects. [provided by RefSeq, Jul 2008]","start":48917768,"end":48921740,"strand":-1,"description":"snail family transcriptional repressor 2 [Source:HGNC Symbol;Acc:HGNC:11094]"}, {"versioned_ensembl_gene_id":"ENSG00000249239.2","gene_symbol":"AC095059.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92821986,"end":92822918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079385.21","gene_symbol":"CEACAM1","gene_name":"carcinoembryonic antigen related cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:1814]","synonyms":"CD66a,BGP1,BGP","biotype":"protein_coding","ncbi_id":"634","summary":"This gene encodes a member of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily. Two subgroups of the CEA family, the CEA cell adhesion molecules and the pregnancy-specific glycoproteins, are located within a 1.2 Mb cluster on the long arm of chromosome 19. Eleven pseudogenes of the CEA cell adhesion molecule subgroup are also found in the cluster. The encoded protein was originally described in bile ducts of liver as biliary glycoprotein. Subsequently, it was found to be a cell-cell adhesion molecule detected on leukocytes, epithelia, and endothelia. The encoded protein mediates cell adhesion via homophilic as well as heterophilic binding to other proteins of the subgroup. Multiple cellular activities have been attributed to the encoded protein, including roles in the differentiation and arrangement of tissue three-dimensional structure, angiogenesis, apoptosis, tumor suppression, metastasis, and the modulation of innate and adaptive immune responses. Multiple transcript variants encoding different isoforms have been reported, but the full-length nature of all variants has not been defined. [provided by RefSeq, May 2010]","start":42507304,"end":42561234,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:1814]"}, {"versioned_ensembl_gene_id":"ENSG00000124469.11","gene_symbol":"CEACAM8","gene_name":"carcinoembryonic antigen related cell adhesion molecule 8 [Source:HGNC Symbol;Acc:HGNC:1820]","synonyms":"CGM6,CD66b","biotype":"protein_coding","ncbi_id":"1088","summary":null,"start":42580241,"end":42595055,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 8 [Source:HGNC Symbol;Acc:HGNC:1820]"}, {"versioned_ensembl_gene_id":"ENSG00000268605.1","gene_symbol":"AC011497.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42424384,"end":42425071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224106.1","gene_symbol":"CYP4F25P","gene_name":"cytochrome P450 family 4 subfamily F member 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:39949]","synonyms":"CYP4F-se1[6:8]","biotype":"unprocessed_pseudogene","ncbi_id":"100288827","summary":null,"start":64465463,"end":64466498,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:39949]"}, {"versioned_ensembl_gene_id":"ENSG00000269374.1","gene_symbol":"AC011497.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42485076,"end":42485714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071205.11","gene_symbol":"ARHGAP10","gene_name":"Rho GTPase activating protein 10 [Source:HGNC Symbol;Acc:HGNC:26099]","synonyms":"FLJ41791,FLJ20896,GRAF2","biotype":"protein_coding","ncbi_id":"79658","summary":null,"start":147732063,"end":148072780,"strand":1,"description":"Rho GTPase activating protein 10 [Source:HGNC Symbol;Acc:HGNC:26099]"}, {"versioned_ensembl_gene_id":"ENSG00000148175.12","gene_symbol":"STOM","gene_name":"stomatin [Source:HGNC Symbol;Acc:HGNC:3383]","synonyms":"EPB72,EPB7,BND7","biotype":"protein_coding","ncbi_id":"2040","summary":"This gene encodes a member of a highly conserved family of integral membrane proteins. The encoded protein localizes to the cell membrane of red blood cells and other cell types, where it may regulate ion channels and transporters. Loss of localization of the encoded protein is associated with hereditary stomatocytosis, a form of hemolytic anemia. There is a pseudogene for this gene on chromosome 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":121338988,"end":121370304,"strand":-1,"description":"stomatin [Source:HGNC Symbol;Acc:HGNC:3383]"}, {"versioned_ensembl_gene_id":"ENSG00000048052.21","gene_symbol":"HDAC9","gene_name":"histone deacetylase 9 [Source:HGNC Symbol;Acc:HGNC:14065]","synonyms":"MITR,KIAA0744,HDAC7B,HDAC,HD7","biotype":"protein_coding","ncbi_id":"9734","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene has sequence homology to members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic domain. It represses MEF2 activity through recruitment of multicomponent corepressor complexes that include CtBP and HDACs. This encoded protein may play a role in hematopoiesis. Multiple alternatively spliced transcripts have been described for this gene but the full-length nature of some of them has not been determined. [provided by RefSeq, Jul 2008]","start":18086949,"end":19002416,"strand":1,"description":"histone deacetylase 9 [Source:HGNC Symbol;Acc:HGNC:14065]"}, {"versioned_ensembl_gene_id":"ENSG00000249744.1","gene_symbol":"AC010374.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29848684,"end":29849218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033170.16","gene_symbol":"FUT8","gene_name":"fucosyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:4019]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2530","summary":"This gene encodes an enzyme belonging to the family of fucosyltransferases. The product of this gene catalyzes the transfer of fucose from GDP-fucose to N-linked type complex glycopeptides. This enzyme is distinct from other fucosyltransferases which catalyze alpha1-2, alpha1-3, and alpha1-4 fucose addition. The expression of this gene may contribute to the malignancy of cancer cells and to their invasive and metastatic capabilities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]","start":65410592,"end":65744121,"strand":1,"description":"fucosyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:4019]"}, {"versioned_ensembl_gene_id":"ENSG00000165282.13","gene_symbol":"PIGO","gene_name":"phosphatidylinositol glycan anchor biosynthesis class O [Source:HGNC Symbol;Acc:HGNC:23215]","synonyms":"FLJ00135,DKFZp434M222","biotype":"protein_coding","ncbi_id":"84720","summary":"This gene encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid which contains three mannose molecules in its core backbone. The GPI-anchor is found on many blood cells and serves to anchor proteins to the cell surface. This protein is involved in the transfer of ethanolaminephosphate (EtNP) to the third mannose in GPI. At least three alternatively spliced transcripts encoding two distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":35088688,"end":35096601,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class O [Source:HGNC Symbol;Acc:HGNC:23215]"}, {"versioned_ensembl_gene_id":"ENSG00000260452.1","gene_symbol":"TPRKBP2","gene_name":"TP53RK binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44944]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480804","summary":null,"start":28111173,"end":28111647,"strand":-1,"description":"TP53RK binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44944]"}, {"versioned_ensembl_gene_id":"ENSG00000243179.1","gene_symbol":"AC110769.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113979909,"end":113983258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215548.2","gene_symbol":"FRG1JP","gene_name":"FSHD region gene 1 family member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:51768]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642236","summary":null,"start":63832127,"end":63859641,"strand":-1,"description":"FSHD region gene 1 family member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:51768]"}, {"versioned_ensembl_gene_id":"ENSG00000189090.7","gene_symbol":"FAM25G","gene_name":"family with sequence similarity 25 member G [Source:HGNC Symbol;Acc:HGNC:23590]","synonyms":"bA301J7.4","biotype":"protein_coding","ncbi_id":"100133093","summary":null,"start":47487219,"end":47491693,"strand":-1,"description":"family with sequence similarity 25 member G [Source:HGNC Symbol;Acc:HGNC:23590]"}, {"versioned_ensembl_gene_id":"ENSG00000284505.1","gene_symbol":"LYNX1","gene_name":"Ly6/neurotoxin 1 [Source:NCBI gene;Acc:66004]","synonyms":"SLURP2,SLURP2","biotype":"protein_coding","ncbi_id":"66004","summary":"This gene encodes a GPI-anchored, cell membrane bound member of the Ly6/uPAR (LU) superfamily of proteins containing the unique three-finger LU domain. This protein interacts with nicotinic acetylcholine receptors (nAChRs), and is thought to function as a modulator of nAChR activity to prevent excessive excitation. Alternatively spliced transcript variants have been found for this gene. Read-through transcription between this gene and the neighboring downstream gene (SLURP2) generates naturally-occurring transcripts (LYNX1-SLURP2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Sep 2017]","start":142764334,"end":142778224,"strand":-1,"description":"Ly6/neurotoxin 1 [Source:NCBI gene;Acc:66004]"}, {"versioned_ensembl_gene_id":"ENSG00000141371.12","gene_symbol":"C17orf64","gene_name":"chromosome 17 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:26990]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124773","summary":null,"start":60392429,"end":60431421,"strand":1,"description":"chromosome 17 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:26990]"}, {"versioned_ensembl_gene_id":"ENSG00000229989.3","gene_symbol":"MIR181A1HG","gene_name":"MIR181A1 host gene [Source:HGNC Symbol;Acc:HGNC:48659]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100131234","summary":null,"start":198807493,"end":198937429,"strand":-1,"description":"MIR181A1 host gene [Source:HGNC Symbol;Acc:HGNC:48659]"}, {"versioned_ensembl_gene_id":"ENSG00000267095.1","gene_symbol":"AC025048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60135762,"end":60140081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273336.1","gene_symbol":"OR7M1P","gene_name":"olfactory receptor family 7 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15128]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81352","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":133481238,"end":133481770,"strand":1,"description":"olfactory receptor family 7 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15128]"}, {"versioned_ensembl_gene_id":"ENSG00000263107.1","gene_symbol":"AC025627.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19582116,"end":19582275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267295.1","gene_symbol":"AC025048.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60113793,"end":60120687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280852.2","gene_symbol":"AC025048.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":60101759,"end":60102919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172901.19","gene_symbol":"LVRN","gene_name":"laeverin [Source:HGNC Symbol;Acc:HGNC:26904]","synonyms":"TAQPEP,FLJ90650,AQPEP,APQ","biotype":"protein_coding","ncbi_id":"206338","summary":null,"start":115962454,"end":116027619,"strand":1,"description":"laeverin [Source:HGNC Symbol;Acc:HGNC:26904]"}, {"versioned_ensembl_gene_id":"ENSG00000248490.1","gene_symbol":"AC113355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27412613,"end":27436411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269873.1","gene_symbol":"AC245884.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54438010,"end":54438346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122490.18","gene_symbol":"PQLC1","gene_name":"PQ loop repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:26188]","synonyms":"FLJ22378","biotype":"protein_coding","ncbi_id":"80148","summary":null,"start":79902420,"end":79951664,"strand":-1,"description":"PQ loop repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:26188]"}, {"versioned_ensembl_gene_id":"ENSG00000254871.1","gene_symbol":"AC024475.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46142716,"end":46143594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117133.10","gene_symbol":"RPF1","gene_name":"ribosome production factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:30350]","synonyms":"BXDC5","biotype":"protein_coding","ncbi_id":"80135","summary":null,"start":84479259,"end":84497790,"strand":1,"description":"ribosome production factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:30350]"}, {"versioned_ensembl_gene_id":"ENSG00000261817.1","gene_symbol":"AL390718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180117140,"end":180123890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228331.2","gene_symbol":"AC004448.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19496943,"end":19497528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126233.1","gene_symbol":"SLURP1","gene_name":"secreted LY6/PLAUR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18746]","synonyms":"MDM,LY6LS,ArsB,ARS,ANUP","biotype":"protein_coding","ncbi_id":"57152","summary":"The protein encoded by this gene is a member of the Ly6/uPAR family but lacks a GPI-anchoring signal sequence. It is thought that this secreted protein contains antitumor activity. Mutations in this gene have been associated with Mal de Meleda, a rare autosomal recessive skin disorder. This gene maps to the same chromosomal region as several members of the Ly6/uPAR family of glycoprotein receptors. [provided by RefSeq, Jul 2008]","start":142740944,"end":142742411,"strand":-1,"description":"secreted LY6/PLAUR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18746]"}, {"versioned_ensembl_gene_id":"ENSG00000122432.17","gene_symbol":"SPATA1","gene_name":"spermatogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:14682]","synonyms":"SP-2","biotype":"protein_coding","ncbi_id":"100505741","summary":null,"start":84506300,"end":84566194,"strand":1,"description":"spermatogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:14682]"}, {"versioned_ensembl_gene_id":"ENSG00000226020.4","gene_symbol":"CDK2AP2P3","gene_name":"cyclin dependent kinase 2 associated protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38494]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401525","summary":null,"start":63774870,"end":63775241,"strand":-1,"description":"cyclin dependent kinase 2 associated protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38494]"}, {"versioned_ensembl_gene_id":"ENSG00000228322.1","gene_symbol":"AL162419.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4299390,"end":4306046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145919.10","gene_symbol":"BOD1","gene_name":"biorientation of chromosomes in cell division 1 [Source:HGNC Symbol;Acc:HGNC:25114]","synonyms":"FAM44B","biotype":"protein_coding","ncbi_id":"91272","summary":null,"start":173607514,"end":173616660,"strand":-1,"description":"biorientation of chromosomes in cell division 1 [Source:HGNC Symbol;Acc:HGNC:25114]"}, {"versioned_ensembl_gene_id":"ENSG00000164485.14","gene_symbol":"IL22RA2","gene_name":"interleukin 22 receptor subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:14901]","synonyms":"IL-22BP,CRF2-S1","biotype":"protein_coding","ncbi_id":"116379","summary":"This gene encodes a member of the class II cytokine receptor family. The encoded soluble protein specifically binds to and inhibits interleukin 22 activity by blocking the interaction of interleukin 22 with its cell surface receptor. The encoded protein may be important in the regulation of inflammatory response, and has been implicated in the regulation of tumorigenesis in the colon. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]","start":137143820,"end":137173648,"strand":-1,"description":"interleukin 22 receptor subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:14901]"}, {"versioned_ensembl_gene_id":"ENSG00000278272.1","gene_symbol":"HIST1H3C","gene_name":"histone cluster 1 H3 family member c [Source:HGNC Symbol;Acc:HGNC:4768]","synonyms":"H3FC,H3/c,H3.1","biotype":"protein_coding","ncbi_id":"8352","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26045411,"end":26045821,"strand":1,"description":"histone cluster 1 H3 family member c [Source:HGNC Symbol;Acc:HGNC:4768]"}, {"versioned_ensembl_gene_id":"ENSG00000136449.13","gene_symbol":"MYCBPAP","gene_name":"MYCBP associated protein [Source:HGNC Symbol;Acc:HGNC:19677]","synonyms":"DKFZp434N1415,AMAP-1","biotype":"protein_coding","ncbi_id":"84073","summary":null,"start":50508384,"end":50531501,"strand":1,"description":"MYCBP associated protein [Source:HGNC Symbol;Acc:HGNC:19677]"}, {"versioned_ensembl_gene_id":"ENSG00000241343.9","gene_symbol":"RPL36A","gene_name":"ribosomal protein L36a [Source:HGNC Symbol;Acc:HGNC:10359]","synonyms":"RPL44,L36A","biotype":"protein_coding","ncbi_id":"6173","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which shares sequence similarity with yeast ribosomal protein L44, belongs to the L44E (L36AE) family of ribosomal proteins. Although this gene has been referred to as ribosomal protein L44 (RPL44), its official name is ribosomal protein L36a (RPL36A). This gene and the human gene officially named ribosomal protein L36a-like (RPL36AL) encode nearly identical proteins; however, they are distinct genes. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Naturally occurring read-through transcription occurs between this locus and the heterogeneous nuclear ribonucleoprotein H2 (H') gene. [provided by RefSeq, Jan 2011]","start":101390824,"end":101396154,"strand":1,"description":"ribosomal protein L36a [Source:HGNC Symbol;Acc:HGNC:10359]"}, {"versioned_ensembl_gene_id":"ENSG00000255008.2","gene_symbol":"AP000442.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59561146,"end":59566074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100626.16","gene_symbol":"GALNT16","gene_name":"polypeptide N-acetylgalactosaminyltransferase 16 [Source:HGNC Symbol;Acc:HGNC:23233]","synonyms":"KIAA1130,GALNTL1,GalNAc-T16","biotype":"protein_coding","ncbi_id":"57452","summary":null,"start":69259277,"end":69357033,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 16 [Source:HGNC Symbol;Acc:HGNC:23233]"}, {"versioned_ensembl_gene_id":"ENSG00000223528.7","gene_symbol":"AL359094.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126988095,"end":127026507,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100711.13","gene_symbol":"ZFYVE21","gene_name":"zinc finger FYVE-type containing 21 [Source:HGNC Symbol;Acc:HGNC:20760]","synonyms":"ZF21,MGC2550","biotype":"protein_coding","ncbi_id":"79038","summary":null,"start":103715730,"end":103733668,"strand":1,"description":"zinc finger FYVE-type containing 21 [Source:HGNC Symbol;Acc:HGNC:20760]"}, {"versioned_ensembl_gene_id":"ENSG00000145721.11","gene_symbol":"LIX1","gene_name":"limb and CNS expressed 1 [Source:HGNC Symbol;Acc:HGNC:18581]","synonyms":"Lft,C5orf11","biotype":"protein_coding","ncbi_id":"167410","summary":null,"start":97091867,"end":97142872,"strand":-1,"description":"limb and CNS expressed 1 [Source:HGNC Symbol;Acc:HGNC:18581]"}, {"versioned_ensembl_gene_id":"ENSG00000251054.1","gene_symbol":"AC008883.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97223371,"end":97227957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259358.1","gene_symbol":"AC026951.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31765743,"end":31768201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276934.1","gene_symbol":"AC009704.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74504766,"end":74505248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205584.6","gene_symbol":"AC211476.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72969814,"end":72971727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115380.19","gene_symbol":"EFEMP1","gene_name":"EGF containing fibulin like extracellular matrix protein 1 [Source:HGNC Symbol;Acc:HGNC:3218]","synonyms":"S1-5,MTLV,FBNL,FBLN3,DHRD","biotype":"protein_coding","ncbi_id":"2202","summary":"This gene encodes a member of the fibulin family of extracellular matrix glycoproteins. Like all members of this family, the encoded protein contains tandemly repeated epidermal growth factor-like repeats followed by a C-terminus fibulin-type domain. This gene is upregulated in malignant gliomas and may play a role in the aggressive nature of these tumors. Mutations in this gene are associated with Doyne honeycomb retinal dystrophy. Alternatively spliced transcript variants that encode the same protein have been described.[provided by RefSeq, Nov 2009]","start":55865967,"end":55924139,"strand":-1,"description":"EGF containing fibulin like extracellular matrix protein 1 [Source:HGNC Symbol;Acc:HGNC:3218]"}, {"versioned_ensembl_gene_id":"ENSG00000117411.16","gene_symbol":"B4GALT2","gene_name":"beta-1,4-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:925]","synonyms":"beta4Gal-T2","biotype":"protein_coding","ncbi_id":"8704","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. The enzyme encoded by this gene synthesizes N-acetyllactosamine in glycolipids and glycoproteins. Its substrate specificity is affected by alpha-lactalbumin but it is not expressed in lactating mammary tissue. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":43978943,"end":43991170,"strand":1,"description":"beta-1,4-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:925]"}, {"versioned_ensembl_gene_id":"ENSG00000266992.1","gene_symbol":"DHX40P1","gene_name":"DEAH-box helicase 40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20687]","synonyms":"DHX40P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107133522","summary":null,"start":59976009,"end":60002384,"strand":-1,"description":"DEAH-box helicase 40 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20687]"}, {"versioned_ensembl_gene_id":"ENSG00000164252.12","gene_symbol":"AGGF1","gene_name":"angiogenic factor with G-patch and FHA domains 1 [Source:HGNC Symbol;Acc:HGNC:24684]","synonyms":"VG5Q,HSU84971,GPATCH7,GPATC7,FLJ10283","biotype":"protein_coding","ncbi_id":"55109","summary":"This gene encodes an angiogenic factor that promotes proliferation of endothelial cells. Mutations in this gene are associated with a susceptibility to Klippel-Trenaunay syndrome. Pseudogenes of this gene are found on chromosomes 3, 4, 10 and 16.[provided by RefSeq, Sep 2010]","start":77029251,"end":77065234,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 [Source:HGNC Symbol;Acc:HGNC:24684]"}, {"versioned_ensembl_gene_id":"ENSG00000169756.16","gene_symbol":"LIMS1","gene_name":"LIM zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:6616]","synonyms":"PINCH1,PINCH","biotype":"protein_coding","ncbi_id":"3987","summary":"The protein encoded by this gene is an adaptor protein which contains five LIM domains, or double zinc fingers. The protein is likely involved in integrin signaling through its LIM domain-mediated interaction with integrin-linked kinase, found in focal adhesion plaques. It is also thought to act as a bridge linking integrin-linked kinase to NCK adaptor protein 2, which is involved in growth factor receptor kinase signaling pathways. Its localization to the periphery of spreading cells also suggests that this protein may play a role in integrin-mediated cell adhesion or spreading. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":108534355,"end":108687246,"strand":1,"description":"LIM zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:6616]"}, {"versioned_ensembl_gene_id":"ENSG00000224856.2","gene_symbol":"AL035398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43957027,"end":43957348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259944.1","gene_symbol":"CDRT7","gene_name":"CMT1A duplicated region transcript 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14386]","synonyms":"NCRNA00025,LINC00025","biotype":"lincRNA","ncbi_id":"94150","summary":null,"start":15030975,"end":15031957,"strand":1,"description":"CMT1A duplicated region transcript 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14386]"}, {"versioned_ensembl_gene_id":"ENSG00000226156.1","gene_symbol":"RPL23AP76","gene_name":"ribosomal protein L23a pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:36555]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441781","summary":null,"start":14947741,"end":14948198,"strand":-1,"description":"ribosomal protein L23a pseudogene 76 [Source:HGNC Symbol;Acc:HGNC:36555]"}, {"versioned_ensembl_gene_id":"ENSG00000230897.1","gene_symbol":"AC013248.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14705076,"end":14705534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237885.1","gene_symbol":"AL359672.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95031640,"end":95032048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135437.9","gene_symbol":"RDH5","gene_name":"retinol dehydrogenase 5 [Source:HGNC Symbol;Acc:HGNC:9940]","synonyms":"SDR9C5,RDH1,HSD17B9","biotype":"protein_coding","ncbi_id":"5959","summary":"This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene. [provided by RefSeq, Dec 2010]","start":55720367,"end":55724705,"strand":1,"description":"retinol dehydrogenase 5 [Source:HGNC Symbol;Acc:HGNC:9940]"}, {"versioned_ensembl_gene_id":"ENSG00000277688.1","gene_symbol":"AC243585.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37609739,"end":37613841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214797.3","gene_symbol":"AP002358.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59268876,"end":59284033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256234.1","gene_symbol":"AC022509.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26211164,"end":26335856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205300.3","gene_symbol":"AL356414.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4070152,"end":4075165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124214.19","gene_symbol":"STAU1","gene_name":"staufen double-stranded RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11370]","synonyms":"STAU,PPP1R150","biotype":"protein_coding","ncbi_id":"6780","summary":"Staufen is a member of the family of double-stranded RNA (dsRNA)-binding proteins involved in the transport and/or localization of mRNAs to different subcellular compartments and/or organelles. These proteins are characterized by the presence of multiple dsRNA-binding domains which are required to bind RNAs having double-stranded secondary structures. The human homologue of staufen encoded by STAU, in addition contains a microtubule- binding domain similar to that of microtubule-associated protein 1B, and binds tubulin. The STAU gene product has been shown to be present in the cytoplasm in association with the rough endoplasmic reticulum (RER), implicating this protein in the transport of mRNA via the microtubule network to the RER, the site of translation. [provided by RefSeq, Apr 2020]","start":49113339,"end":49188367,"strand":-1,"description":"staufen double-stranded RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11370]"}, {"versioned_ensembl_gene_id":"ENSG00000155428.12","gene_symbol":"TRIM74","gene_name":"tripartite motif containing 74 [Source:HGNC Symbol;Acc:HGNC:17453]","synonyms":"TRIM50C,MGC45440","biotype":"protein_coding","ncbi_id":"378108","summary":null,"start":72959485,"end":72969466,"strand":-1,"description":"tripartite motif containing 74 [Source:HGNC Symbol;Acc:HGNC:17453]"}, {"versioned_ensembl_gene_id":"ENSG00000196171.3","gene_symbol":"OR6K2","gene_name":"olfactory receptor family 6 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15029]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81448","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158699678,"end":158700652,"strand":-1,"description":"olfactory receptor family 6 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15029]"}, {"versioned_ensembl_gene_id":"ENSG00000283515.1","gene_symbol":"AC020915.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":58228914,"end":58315183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269794.1","gene_symbol":"AC010642.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58319277,"end":58320489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235102.1","gene_symbol":"ADI1P1","gene_name":"acireductone dioxygenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130936","summary":null,"start":41331123,"end":41331660,"strand":1,"description":"acireductone dioxygenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52339]"}, {"versioned_ensembl_gene_id":"ENSG00000228925.1","gene_symbol":"AC016722.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46899275,"end":46908678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198336.9","gene_symbol":"MYL4","gene_name":"myosin light chain 4 [Source:HGNC Symbol;Acc:HGNC:7585]","synonyms":"PRO1957,GT1,AMLC,ALC1","biotype":"protein_coding","ncbi_id":"4635","summary":"Myosin is a hexameric ATPase cellular motor protein. It is composed of two myosin heavy chains, two nonphosphorylatable myosin alkali light chains, and two phosphorylatable myosin regulatory light chains. This gene encodes a myosin alkali light chain that is found in embryonic muscle and adult atria. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":47200446,"end":47223679,"strand":1,"description":"myosin light chain 4 [Source:HGNC Symbol;Acc:HGNC:7585]"}, {"versioned_ensembl_gene_id":"ENSG00000215093.3","gene_symbol":"EEF1A1P29","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:37904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130211","summary":null,"start":86160264,"end":86161359,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:37904]"}, {"versioned_ensembl_gene_id":"ENSG00000236433.1","gene_symbol":"RPL37P21","gene_name":"ribosomal protein L37 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36256]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271516","summary":null,"start":68331338,"end":68331613,"strand":-1,"description":"ribosomal protein L37 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36256]"}, {"versioned_ensembl_gene_id":"ENSG00000253785.1","gene_symbol":"AC008429.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172975511,"end":172976374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215386.11","gene_symbol":"MIR99AHG","gene_name":"mir-99a-let-7c cluster host gene [Source:HGNC Symbol;Acc:HGNC:1274]","synonyms":"MONC,LINC00478,FLJ38295,C21orf35,C21orf34","biotype":"lincRNA","ncbi_id":"388815","summary":null,"start":15928296,"end":16627397,"strand":1,"description":"mir-99a-let-7c cluster host gene [Source:HGNC Symbol;Acc:HGNC:1274]"}, {"versioned_ensembl_gene_id":"ENSG00000197457.9","gene_symbol":"STMN3","gene_name":"stathmin 3 [Source:HGNC Symbol;Acc:HGNC:15926]","synonyms":"SCLIP","biotype":"protein_coding","ncbi_id":"50861","summary":"This gene encodes a protein which is a member of the stathmin protein family. Members of this protein family form a complex with tubulins at a ratio of 2 tubulins for each stathmin protein. Microtubules require the ordered assembly of alpha- and beta-tubulins, and formation of a complex with stathmin disrupts microtubule formation and function. A pseudogene of this gene is located on chromosome 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":63639705,"end":63657682,"strand":-1,"description":"stathmin 3 [Source:HGNC Symbol;Acc:HGNC:15926]"}, {"versioned_ensembl_gene_id":"ENSG00000130826.17","gene_symbol":"DKC1","gene_name":"dyskerin pseudouridine synthase 1 [Source:HGNC Symbol;Acc:HGNC:2890]","synonyms":"XAP101,NOLA4,NAP57,dyskerin,DKC,Cbf5","biotype":"protein_coding","ncbi_id":"1736","summary":"This gene functions in two distinct complexes. It plays an active role in telomerase stabilization and maintenance, as well as recognition of snoRNAs containing H/ACA sequences which provides stability during biogenesis and assembly into H/ACA small nucleolar RNA ribonucleoproteins (snoRNPs). This gene is highly conserved and widely expressed, and may play additional roles in nucleo-cytoplasmic shuttling, DNA damage response, and cell adhesion. Mutations have been associated with X-linked dyskeratosis congenita. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":154762742,"end":154777689,"strand":1,"description":"dyskerin pseudouridine synthase 1 [Source:HGNC Symbol;Acc:HGNC:2890]"}, {"versioned_ensembl_gene_id":"ENSG00000197241.3","gene_symbol":"SLC2A7","gene_name":"solute carrier family 2 member 7 [Source:HGNC Symbol;Acc:HGNC:13445]","synonyms":"GLUT7","biotype":"protein_coding","ncbi_id":"155184","summary":"SLC2A7 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Li et al., 2004). This family of transporters shows conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]","start":9003300,"end":9026345,"strand":-1,"description":"solute carrier family 2 member 7 [Source:HGNC Symbol;Acc:HGNC:13445]"}, {"versioned_ensembl_gene_id":"ENSG00000142892.14","gene_symbol":"PIGK","gene_name":"phosphatidylinositol glycan anchor biosynthesis class K [Source:HGNC Symbol;Acc:HGNC:8965]","synonyms":"hGPI8,GPI8","biotype":"protein_coding","ncbi_id":"10026","summary":"This gene encodes a member of the cysteine protease family C13 that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This protein is a member of the multisubunit enzyme, GPI transamidase and is thought to be its enzymatic component. GPI transamidase mediates GPI anchoring in the endoplasmic reticulum, by catalyzing the transfer of fully assembled GPI units to proteins. [provided by RefSeq, Jul 2008]","start":77088990,"end":77219430,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class K [Source:HGNC Symbol;Acc:HGNC:8965]"}, {"versioned_ensembl_gene_id":"ENSG00000272379.1","gene_symbol":"AL008729.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13290018,"end":13290490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175294.5","gene_symbol":"CATSPER1","gene_name":"cation channel sperm associated 1 [Source:HGNC Symbol;Acc:HGNC:17116]","synonyms":"CATSPER","biotype":"protein_coding","ncbi_id":"117144","summary":"Calcium ions play a primary role in the regulation of sperm motility. This gene belongs to a family of putative cation channels that are specific to spermatozoa and localize to the flagellum. The protein family features a single repeat with six membrane-spanning segments and a predicted calcium-selective pore region. [provided by RefSeq, Jul 2008]","start":66016752,"end":66026517,"strand":-1,"description":"cation channel sperm associated 1 [Source:HGNC Symbol;Acc:HGNC:17116]"}, {"versioned_ensembl_gene_id":"ENSG00000232663.2","gene_symbol":"AL139415.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8909742,"end":8909904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159556.9","gene_symbol":"ISL2","gene_name":"ISL LIM homeobox 2 [Source:HGNC Symbol;Acc:HGNC:18524]","synonyms":"FLJ10160","biotype":"protein_coding","ncbi_id":"64843","summary":null,"start":76336724,"end":76342476,"strand":1,"description":"ISL LIM homeobox 2 [Source:HGNC Symbol;Acc:HGNC:18524]"}, {"versioned_ensembl_gene_id":"ENSG00000232354.8","gene_symbol":"VIPR1-AS1","gene_name":"VIPR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40610]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874007","summary":null,"start":42506465,"end":42533258,"strand":-1,"description":"VIPR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40610]"}, {"versioned_ensembl_gene_id":"ENSG00000269807.1","gene_symbol":"AC007292.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4347244,"end":4354057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226563.3","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"bQB90C11.3,HCG4P6,HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29916754,"end":29917744,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000272814.1","gene_symbol":"AC093732.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46956615,"end":46956888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247151.6","gene_symbol":"CSTF3-AS1","gene_name":"CSTF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27882]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338739","summary":null,"start":33161657,"end":33191598,"strand":1,"description":"CSTF3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27882]"}, {"versioned_ensembl_gene_id":"ENSG00000278863.1","gene_symbol":"AC091059.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":59362665,"end":59363278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255452.1","gene_symbol":"AC084851.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49092404,"end":49092767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137573.13","gene_symbol":"SULF1","gene_name":"sulfatase 1 [Source:HGNC Symbol;Acc:HGNC:20391]","synonyms":"SULF-1,KIAA1077,hSulf-1","biotype":"protein_coding","ncbi_id":"23213","summary":"This gene encodes an extracellular heparan sulfate endosulfatase. The encoded enzyme selectively removes 6-O-sulfate groups from heparan sulfate chains of heparan sulfate proteoglycans (HSPGs). The enzyme is secreted through the Golgi and is subsequently localized to the cell surface. The expression of this gene may be down-regulated in several types of cancer, including hepatocellular (HCC), ovarian and breast cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":69466624,"end":69660915,"strand":1,"description":"sulfatase 1 [Source:HGNC Symbol;Acc:HGNC:20391]"}, {"versioned_ensembl_gene_id":"ENSG00000163554.12","gene_symbol":"SPTA1","gene_name":"spectrin alpha, erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11272]","synonyms":"EL2","biotype":"protein_coding","ncbi_id":"6708","summary":"This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [provided by RefSeq, Aug 2017]","start":158610706,"end":158686698,"strand":-1,"description":"spectrin alpha, erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11272]"}, {"versioned_ensembl_gene_id":"ENSG00000234665.8","gene_symbol":"AL512625.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62856999,"end":62898087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153976.2","gene_symbol":"HS3ST3A1","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 3A1 [Source:HGNC Symbol;Acc:HGNC:5196]","synonyms":"3OST3A1,30ST3A1","biotype":"protein_coding","ncbi_id":"9955","summary":"Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. The enzyme encoded by this gene is a member of the heparan sulfate biosynthetic enzyme family. It is a type II integral membrane protein and possesses heparan sulfate glucosaminyl 3-O-sulfotransferase activity. The sulfotransferase domain of this enzyme is highly similar to the same domain of heparan sulfate D-glucosaminyl 3-O-sulfotransferase 3B1, and these two enzymes sulfate an identical disaccharide. This gene is widely expressed, with the most abundant expression in liver and placenta. [provided by RefSeq, Dec 2014]","start":13495689,"end":13601927,"strand":-1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 3A1 [Source:HGNC Symbol;Acc:HGNC:5196]"}, {"versioned_ensembl_gene_id":"ENSG00000229422.1","gene_symbol":"AL512625.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62837748,"end":62838372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256465.1","gene_symbol":"AC023050.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31893370,"end":31893702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134308.13","gene_symbol":"YWHAQ","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta [Source:HGNC Symbol;Acc:HGNC:12854]","synonyms":"HS1,14-3-3","biotype":"protein_coding","ncbi_id":"10971","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 99% identical to the mouse and rat orthologs. This gene is upregulated in patients with amyotrophic lateral sclerosis. It contains in its 5' UTR a 6 bp tandem repeat sequence which is polymorphic, however, there is no correlation between the repeat number and the disease. [provided by RefSeq, Jul 2008]","start":9583972,"end":9631014,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta [Source:HGNC Symbol;Acc:HGNC:12854]"}, {"versioned_ensembl_gene_id":"ENSG00000255760.1","gene_symbol":"LINC02422","gene_name":"long intergenic non-protein coding RNA 2422 [Source:HGNC Symbol;Acc:HGNC:53352]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369723","summary":null,"start":31877079,"end":31887203,"strand":-1,"description":"long intergenic non-protein coding RNA 2422 [Source:HGNC Symbol;Acc:HGNC:53352]"}, {"versioned_ensembl_gene_id":"ENSG00000237968.1","gene_symbol":"AC007322.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21940012,"end":21941593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259873.1","gene_symbol":"AC009117.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82434828,"end":82435381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261285.5","gene_symbol":"AC009117.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82495993,"end":82510919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234159.1","gene_symbol":"RBPMSLP","gene_name":"RNA binding protein with multiple splicing-like pseudogene [Source:HGNC Symbol;Acc:HGNC:9923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54032","summary":null,"start":15744004,"end":15745080,"strand":-1,"description":"RNA binding protein with multiple splicing-like pseudogene [Source:HGNC Symbol;Acc:HGNC:9923]"}, {"versioned_ensembl_gene_id":"ENSG00000100644.16","gene_symbol":"HIF1A","gene_name":"hypoxia inducible factor 1 alpha subunit [Source:HGNC Symbol;Acc:HGNC:4910]","synonyms":"HIF-1alpha,bHLHe78,PASD8,MOP1,HIF1","biotype":"protein_coding","ncbi_id":"3091","summary":"This gene encodes the alpha subunit of transcription factor hypoxia-inducible factor-1 (HIF-1), which is a heterodimer composed of an alpha and a beta subunit. HIF-1 functions as a master regulator of cellular and systemic homeostatic response to hypoxia by activating transcription of many genes, including those involved in energy metabolism, angiogenesis, apoptosis, and other genes whose protein products increase oxygen delivery or facilitate metabolic adaptation to hypoxia. HIF-1 thus plays an essential role in embryonic vascularization, tumor angiogenesis and pathophysiology of ischemic disease. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2011]","start":61695513,"end":61748259,"strand":1,"description":"hypoxia inducible factor 1 alpha subunit [Source:HGNC Symbol;Acc:HGNC:4910]"}, {"versioned_ensembl_gene_id":"ENSG00000142731.10","gene_symbol":"PLK4","gene_name":"polo like kinase 4 [Source:HGNC Symbol;Acc:HGNC:11397]","synonyms":"STK18,Sak","biotype":"protein_coding","ncbi_id":"10733","summary":"This gene encodes a member of the polo family of serine/threonine protein kinases. The protein localizes to centrioles, complex microtubule-based structures found in centrosomes, and regulates centriole duplication during the cell cycle. Three alternatively spliced transcript variants that encode different protein isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":127880861,"end":127899195,"strand":1,"description":"polo like kinase 4 [Source:HGNC Symbol;Acc:HGNC:11397]"}, {"versioned_ensembl_gene_id":"ENSG00000254517.1","gene_symbol":"AC027369.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48959928,"end":48961810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236656.1","gene_symbol":"AL365440.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158474454,"end":158494886,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196993.8","gene_symbol":"NPIPB9","gene_name":"nuclear pore complex interacting protein family member B9 [Source:HGNC Symbol;Acc:HGNC:41987]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507607","summary":null,"start":28751787,"end":28772807,"strand":1,"description":"nuclear pore complex interacting protein family member B9 [Source:HGNC Symbol;Acc:HGNC:41987]"}, {"versioned_ensembl_gene_id":"ENSG00000170899.10","gene_symbol":"GSTA4","gene_name":"glutathione S-transferase alpha 4 [Source:HGNC Symbol;Acc:HGNC:4629]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2941","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. These enzymes are involved in cellular defense against toxic, carcinogenic, and pharmacologically active electrophilic compounds. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-tranferase belonging to the alpha class. The alpha class genes, which are located in a cluster on chromosome 6, are highly related and encode enzymes with glutathione peroxidase activity that function in the detoxification of lipid peroxidation products. Reactive electrophiles produced by oxidative metabolism have been linked to a number of degenerative diseases including Parkinson's disease, Alzheimer's disease, cataract formation, and atherosclerosis. [provided by RefSeq, Jul 2008]","start":52977948,"end":52995378,"strand":-1,"description":"glutathione S-transferase alpha 4 [Source:HGNC Symbol;Acc:HGNC:4629]"}, {"versioned_ensembl_gene_id":"ENSG00000280064.1","gene_symbol":"AC130304.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37858949,"end":37861333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163393.12","gene_symbol":"SLC22A15","gene_name":"solute carrier family 22 member 15 [Source:HGNC Symbol;Acc:HGNC:20301]","synonyms":"FLIPT1","biotype":"protein_coding","ncbi_id":"55356","summary":"Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, hormones, neurotransmitters, and cellular metabolites. These transporters are also referred to as amphiphilic solute facilitators (ASFs).[supplied by OMIM, Apr 2004]","start":115976498,"end":116070054,"strand":1,"description":"solute carrier family 22 member 15 [Source:HGNC Symbol;Acc:HGNC:20301]"}, {"versioned_ensembl_gene_id":"ENSG00000279838.1","gene_symbol":"AL356273.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":185292384,"end":185294372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248632.1","gene_symbol":"AC106872.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164968587,"end":164970002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177169.9","gene_symbol":"ULK1","gene_name":"unc-51 like autophagy activating kinase 1 [Source:HGNC Symbol;Acc:HGNC:12558]","synonyms":"ATG1A,ATG1","biotype":"protein_coding","ncbi_id":"8408","summary":null,"start":131894651,"end":131923167,"strand":1,"description":"unc-51 like autophagy activating kinase 1 [Source:HGNC Symbol;Acc:HGNC:12558]"}, {"versioned_ensembl_gene_id":"ENSG00000231281.1","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bQB115I13.2,bPG299F13.9,FLJ40123,bCX101P6.9","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31192649,"end":31198853,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000176049.15","gene_symbol":"JAKMIP2","gene_name":"janus kinase and microtubule interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29067]","synonyms":"KIAA0555,JAMIP2","biotype":"protein_coding","ncbi_id":"9832","summary":"The protein encoded by this gene is reported to be a component of the Golgi matrix. It may act as a golgin protein by negatively regulating transit of secretory cargo and by acting as a structural scaffold of the Golgi. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":147585439,"end":147782848,"strand":-1,"description":"janus kinase and microtubule interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29067]"}, {"versioned_ensembl_gene_id":"ENSG00000224001.2","gene_symbol":"AL360081.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98234709,"end":98235567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064547.13","gene_symbol":"LPAR2","gene_name":"lysophosphatidic acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:3168]","synonyms":"EDG-4,LPA2,EDG4","biotype":"protein_coding","ncbi_id":"9170","summary":"This gene encodes a member of family I of the G protein-coupled receptors, as well as the EDG family of proteins. This protein functions as a lysophosphatidic acid (LPA) receptor and contributes to Ca2+ mobilization, a critical cellular response to LPA in cells, through association with Gi and Gq proteins. An alternative splice variant has been described but its full length sequence has not been determined. [provided by RefSeq, Jul 2008]","start":19623668,"end":19628930,"strand":-1,"description":"lysophosphatidic acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:3168]"}, {"versioned_ensembl_gene_id":"ENSG00000228544.1","gene_symbol":"CCDC183-AS1","gene_name":"CCDC183 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44105]","synonyms":"KIAA1984-AS1","biotype":"antisense_RNA","ncbi_id":"100131193","summary":null,"start":136803927,"end":136808848,"strand":-1,"description":"CCDC183 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44105]"}, {"versioned_ensembl_gene_id":"ENSG00000273066.5","gene_symbol":"AL355987.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":136799223,"end":136810042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125148.6","gene_symbol":"MT2A","gene_name":"metallothionein 2A [Source:HGNC Symbol;Acc:HGNC:7406]","synonyms":"MT2","biotype":"protein_coding","ncbi_id":"4502","summary":"This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions, altering the intracellular concentration of heavy metals in the cell. These proteins act as anti-oxidants, protect against hydroxyl free radicals, are important in homeostatic control of metal in the cell, and play a role in detoxification of heavy metals. The encoded protein interacts with the protein encoded by the homeobox containing 1 gene in some cell types, controlling intracellular zinc levels, affecting apoptotic and autophagy pathways. Some polymorphisms in this gene are associated with an increased risk of cancer. [provided by RefSeq, Sep 2017]","start":56608199,"end":56609497,"strand":1,"description":"metallothionein 2A [Source:HGNC Symbol;Acc:HGNC:7406]"}, {"versioned_ensembl_gene_id":"ENSG00000169397.3","gene_symbol":"RNASE3","gene_name":"ribonuclease A family member 3 [Source:HGNC Symbol;Acc:HGNC:10046]","synonyms":"RNS3,RAF1,ECP","biotype":"protein_coding","ncbi_id":"6037","summary":"The protein encoded by this gene belongs to the pancreatic ribonuclease family, a subset of the ribonuclease A superfamily. The protein exhibits antimicrobial activity against pathogenic bacteria [provided by RefSeq, Oct 2014]","start":20891399,"end":20892348,"strand":1,"description":"ribonuclease A family member 3 [Source:HGNC Symbol;Acc:HGNC:10046]"}, {"versioned_ensembl_gene_id":"ENSG00000160161.9","gene_symbol":"CILP2","gene_name":"cartilage intermediate layer protein 2 [Source:HGNC Symbol;Acc:HGNC:24213]","synonyms":"MGC45771","biotype":"protein_coding","ncbi_id":"148113","summary":null,"start":19538248,"end":19546659,"strand":1,"description":"cartilage intermediate layer protein 2 [Source:HGNC Symbol;Acc:HGNC:24213]"}, {"versioned_ensembl_gene_id":"ENSG00000070882.12","gene_symbol":"OSBPL3","gene_name":"oxysterol binding protein like 3 [Source:HGNC Symbol;Acc:HGNC:16370]","synonyms":"OSBP3,ORP3,ORP-3,KIAA0704","biotype":"protein_coding","ncbi_id":"26031","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. The encoded protein is involved in the regulation of cell adhesion and organization of the actin cytoskeleton. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":24796539,"end":24981634,"strand":-1,"description":"oxysterol binding protein like 3 [Source:HGNC Symbol;Acc:HGNC:16370]"}, {"versioned_ensembl_gene_id":"ENSG00000185319.5","gene_symbol":"SSXP4","gene_name":"SSX family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30641]","synonyms":"SSX10,psiSSX4","biotype":"unprocessed_pseudogene","ncbi_id":"326337","summary":null,"start":52598494,"end":52603289,"strand":1,"description":"SSX family pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30641]"}, {"versioned_ensembl_gene_id":"ENSG00000189057.10","gene_symbol":"FAM111B","gene_name":"family with sequence similarity 111 member B [Source:HGNC Symbol;Acc:HGNC:24200]","synonyms":"CANP","biotype":"protein_coding","ncbi_id":"374393","summary":"This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog of this gene which also has a trypsin‐like peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]","start":59107185,"end":59127410,"strand":1,"description":"family with sequence similarity 111 member B [Source:HGNC Symbol;Acc:HGNC:24200]"}, {"versioned_ensembl_gene_id":"ENSG00000259914.1","gene_symbol":"AC009063.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83725676,"end":83726377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261410.1","gene_symbol":"AC009142.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83383007,"end":83398170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280044.1","gene_symbol":"AC099506.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":82727474,"end":82727694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279337.1","gene_symbol":"AC127024.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30724982,"end":30725181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233903.2","gene_symbol":"Z83851.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42276355,"end":42277052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189401.2","gene_symbol":"OTUD6A","gene_name":"OTU deubiquitinase 6A [Source:HGNC Symbol;Acc:HGNC:32312]","synonyms":"HSHIN6,FLJ25831,DUBA2","biotype":"protein_coding","ncbi_id":"139562","summary":"Deubiquitinating enzymes (DUBs; see MIM 603478) are proteases that specifically cleave ubiquitin (MIM 191339) linkages, negating the action of ubiquitin ligases. DUBA2 belongs to a DUB subfamily characterized by an ovarian tumor (OTU) domain.[supplied by OMIM, May 2008]","start":70062491,"end":70064179,"strand":1,"description":"OTU deubiquitinase 6A [Source:HGNC Symbol;Acc:HGNC:32312]"}, {"versioned_ensembl_gene_id":"ENSG00000266915.1","gene_symbol":"MRPS5P4","gene_name":"mitochondrial ribosomal protein S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359797","summary":null,"start":60519841,"end":60520165,"strand":1,"description":"mitochondrial ribosomal protein S5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29779]"}, {"versioned_ensembl_gene_id":"ENSG00000204001.9","gene_symbol":"LCN8","gene_name":"lipocalin 8 [Source:HGNC Symbol;Acc:HGNC:27038]","synonyms":"LCN5","biotype":"protein_coding","ncbi_id":"138307","summary":"Members of the lipocalin family, such as LCN8, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al., 2004 [PubMed 15363845]).[supplied by OMIM, Aug 2009]","start":136754386,"end":136758543,"strand":-1,"description":"lipocalin 8 [Source:HGNC Symbol;Acc:HGNC:27038]"}, {"versioned_ensembl_gene_id":"ENSG00000182057.4","gene_symbol":"OGFRP1","gene_name":"opioid growth factor receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50511]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388906","summary":null,"start":42269753,"end":42275196,"strand":1,"description":"opioid growth factor receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50511]"}, {"versioned_ensembl_gene_id":"ENSG00000232068.1","gene_symbol":"AF003529.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":133989443,"end":133990086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102978.12","gene_symbol":"POLR2C","gene_name":"RNA polymerase II subunit C [Source:HGNC Symbol;Acc:HGNC:9189]","synonyms":"RPB3","biotype":"protein_coding","ncbi_id":"5432","summary":"This gene encodes the third largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene contains a cysteine rich region and exists as a heterodimer with another polymerase subunit, POLR2J. These two subunits form a core subassembly unit of the polymerase. A pseudogene has been identified on chromosome 21. [provided by RefSeq, Jul 2008]","start":57462387,"end":57472010,"strand":1,"description":"RNA polymerase II subunit C [Source:HGNC Symbol;Acc:HGNC:9189]"}, {"versioned_ensembl_gene_id":"ENSG00000224129.1","gene_symbol":"DPPA2P2","gene_name":"developmental pluripotency associated 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44627]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128503","summary":null,"start":26519354,"end":26520250,"strand":-1,"description":"developmental pluripotency associated 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44627]"}, {"versioned_ensembl_gene_id":"ENSG00000234436.1","gene_symbol":"AC245884.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54301758,"end":54306026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240197.1","gene_symbol":"AC245884.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54294049,"end":54294366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106789.12","gene_symbol":"CORO2A","gene_name":"coronin 2A [Source:HGNC Symbol;Acc:HGNC:2255]","synonyms":"WDR2,IR10","biotype":"protein_coding","ncbi_id":"7464","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 5 WD repeats, and has a structural similarity with actin-binding proteins: the D. discoideum coronin and the human p57 protein, suggesting that this protein may also be an actin-binding protein that regulates cell motility. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":98120975,"end":98192640,"strand":-1,"description":"coronin 2A [Source:HGNC Symbol;Acc:HGNC:2255]"}, {"versioned_ensembl_gene_id":"ENSG00000249206.2","gene_symbol":"GCNT1P2","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37972]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421560","summary":null,"start":22580225,"end":22580819,"strand":-1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37972]"}, {"versioned_ensembl_gene_id":"ENSG00000235746.1","gene_symbol":"CTBP2P2","gene_name":"C-terminal binding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45194]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130970","summary":null,"start":94646364,"end":94647996,"strand":-1,"description":"C-terminal binding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45194]"}, {"versioned_ensembl_gene_id":"ENSG00000232964.2","gene_symbol":"LINC01737","gene_name":"long intergenic non-protein coding RNA 1737 [Source:HGNC Symbol;Acc:HGNC:52525]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927553","summary":null,"start":230592660,"end":230595583,"strand":-1,"description":"long intergenic non-protein coding RNA 1737 [Source:HGNC Symbol;Acc:HGNC:52525]"}, {"versioned_ensembl_gene_id":"ENSG00000138442.9","gene_symbol":"WDR12","gene_name":"WD repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:14098]","synonyms":"YTM1,FLJ10881","biotype":"protein_coding","ncbi_id":"55759","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein is highly similar to the mouse WD repeat domain 12 protein at the amino acid level. The protein encoded by this gene is a component of a nucleolar protein complex that affects maturation of the large ribosomal subunit.[provided by RefSeq, Dec 2008]","start":202874782,"end":203014798,"strand":-1,"description":"WD repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:14098]"}, {"versioned_ensembl_gene_id":"ENSG00000264044.1","gene_symbol":"AC005726.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28633206,"end":28635950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167625.10","gene_symbol":"ZNF526","gene_name":"zinc finger protein 526 [Source:HGNC Symbol;Acc:HGNC:29415]","synonyms":"MGC4267,KIAA1951","biotype":"protein_coding","ncbi_id":"116115","summary":null,"start":42220271,"end":42228201,"strand":1,"description":"zinc finger protein 526 [Source:HGNC Symbol;Acc:HGNC:29415]"}, {"versioned_ensembl_gene_id":"ENSG00000154920.14","gene_symbol":"EME1","gene_name":"essential meiotic structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:24965]","synonyms":"SLX2A,MMS4L,FLJ31364","biotype":"protein_coding","ncbi_id":"146956","summary":"This gene encodes a protein that complexes with methyl methanesulfonate-sensitive UV-sensitive 81 protein to form an endonuclease complex. The encoded protein interacts with specifc DNA structures including nicked Holliday junctions, 3'-flap structures and aberrant replication fork structures. This protein may be involved in repairing DNA damage and in maintaining genomic stability. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":50373220,"end":50381483,"strand":1,"description":"essential meiotic structure-specific endonuclease 1 [Source:HGNC Symbol;Acc:HGNC:24965]"}, {"versioned_ensembl_gene_id":"ENSG00000223571.6","gene_symbol":"DHRSX-IT1","gene_name":"DHRSX intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:38713]","synonyms":"DHRSXIT1,DHRSX-IT","biotype":"sense_intronic","ncbi_id":"106478924","summary":null,"start":2334295,"end":2336410,"strand":-1,"description":"DHRSX intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:38713]"}, {"versioned_ensembl_gene_id":"ENSG00000283198.1","gene_symbol":"AL603764.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":122568591,"end":122568911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213023.10","gene_symbol":"SYT3","gene_name":"synaptotagmin 3 [Source:HGNC Symbol;Acc:HGNC:11511]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84258","summary":null,"start":50621307,"end":50639827,"strand":-1,"description":"synaptotagmin 3 [Source:HGNC Symbol;Acc:HGNC:11511]"}, {"versioned_ensembl_gene_id":"ENSG00000241661.1","gene_symbol":"PPP1R2P6","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16321]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130972","summary":null,"start":140292752,"end":140293339,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16321]"}, {"versioned_ensembl_gene_id":"ENSG00000196570.2","gene_symbol":"PFN3","gene_name":"profilin 3 [Source:HGNC Symbol;Acc:HGNC:18627]","synonyms":null,"biotype":"protein_coding","ncbi_id":"345456","summary":"The product of this gene belongs to the profilin family of proteins. This protein binds to actin and affects the structure of the cytoskeleton. It also may be involved in spermatogenesis. It is a single exon gene. [provided by RefSeq, Jul 2008]","start":177400107,"end":177400636,"strand":-1,"description":"profilin 3 [Source:HGNC Symbol;Acc:HGNC:18627]"}, {"versioned_ensembl_gene_id":"ENSG00000168263.8","gene_symbol":"KCNV2","gene_name":"potassium voltage-gated channel modifier subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:19698]","synonyms":"Kv8.2","biotype":"protein_coding","ncbi_id":"169522","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium voltage-gated channel subfamily V. This member is identified as a 'silent subunit', and it does not form homomultimers, but forms heteromultimers with several other subfamily members. Through obligatory heteromerization, it exerts a function-altering effect on other potassium channel subunits. This protein is strongly expressed in pancreas and has a weaker expression in several other tissues. [provided by RefSeq, Jul 2008]","start":2717502,"end":2730037,"strand":1,"description":"potassium voltage-gated channel modifier subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:19698]"}, {"versioned_ensembl_gene_id":"ENSG00000276776.4","gene_symbol":"TC2N","gene_name":"tandem C2 domains, nuclear [Source:HGNC Symbol;Acc:HGNC:19859]","synonyms":"C2CD1,C14orf47,Tac2-N,MTAC2D1,FLJ36557","biotype":"protein_coding","ncbi_id":"123036","summary":null,"start":91783410,"end":91840185,"strand":-1,"description":"tandem C2 domains, nuclear [Source:HGNC Symbol;Acc:HGNC:19859]"}, {"versioned_ensembl_gene_id":"ENSG00000160075.11","gene_symbol":"SSU72","gene_name":"SSU72 homolog, RNA polymerase II CTD phosphatase [Source:HGNC Symbol;Acc:HGNC:25016]","synonyms":"HSPC182","biotype":"protein_coding","ncbi_id":"29101","summary":null,"start":1541673,"end":1574869,"strand":-1,"description":"SSU72 homolog, RNA polymerase II CTD phosphatase [Source:HGNC Symbol;Acc:HGNC:25016]"}, {"versioned_ensembl_gene_id":"ENSG00000166816.13","gene_symbol":"LDHD","gene_name":"lactate dehydrogenase D [Source:HGNC Symbol;Acc:HGNC:19708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"197257","summary":"The protein encoded by this gene belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. The similar protein in yeast has both D-lactate and D-glycerate dehydrogenase activities. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":75111860,"end":75116771,"strand":-1,"description":"lactate dehydrogenase D [Source:HGNC Symbol;Acc:HGNC:19708]"}, {"versioned_ensembl_gene_id":"ENSG00000227477.1","gene_symbol":"STK4-AS1","gene_name":"STK4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43811]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505826","summary":null,"start":44963794,"end":44966402,"strand":-1,"description":"STK4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43811]"}, {"versioned_ensembl_gene_id":"ENSG00000179588.8","gene_symbol":"ZFPM1","gene_name":"zinc finger protein, FOG family member 1 [Source:HGNC Symbol;Acc:HGNC:19762]","synonyms":"ZNF89A,ZC2HC11A,FOG1,FOG","biotype":"protein_coding","ncbi_id":"161882","summary":null,"start":88453317,"end":88537016,"strand":1,"description":"zinc finger protein, FOG family member 1 [Source:HGNC Symbol;Acc:HGNC:19762]"}, {"versioned_ensembl_gene_id":"ENSG00000147160.9","gene_symbol":"AWAT2","gene_name":"acyl-CoA wax alcohol acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:23251]","synonyms":"MFAT,DGAT2L4","biotype":"protein_coding","ncbi_id":"158835","summary":"This gene encodes an enzyme belonging to the diacylglycerol acyltransferase family. This enzyme produces wax esters by the esterification of long chain (or wax) alcohols with acyl-CoA-derived fatty acids. It functions in lipid metabolism in the skin, mostly in undifferentiated peripheral sebocytes. This enzyme may also have acyl-CoA:retinol acyltransferase activities, where it catalyzes the synthesis of diacylglycerols and retinyl esters. [provided by RefSeq, May 2010]","start":70040542,"end":70049938,"strand":-1,"description":"acyl-CoA wax alcohol acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:23251]"}, {"versioned_ensembl_gene_id":"ENSG00000214269.3","gene_symbol":"LGMNP1","gene_name":"legumain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23079]","synonyms":"LGMN2P","biotype":"processed_pseudogene","ncbi_id":"122199","summary":null,"start":64958097,"end":64959396,"strand":-1,"description":"legumain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23079]"}, {"versioned_ensembl_gene_id":"ENSG00000188730.4","gene_symbol":"VWC2","gene_name":"von Willebrand factor C domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30200]","synonyms":"UNQ739,PSST739","biotype":"protein_coding","ncbi_id":"375567","summary":"This gene encodes a secreted bone morphogenic protein antagonist. The encoded protein is possibly involved in neural function and development and may have a role in cell adhesion.[provided by RefSeq, Oct 2009]","start":49773661,"end":49921950,"strand":1,"description":"von Willebrand factor C domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30200]"}, {"versioned_ensembl_gene_id":"ENSG00000167904.14","gene_symbol":"TMEM68","gene_name":"transmembrane protein 68 [Source:HGNC Symbol;Acc:HGNC:26510]","synonyms":"FLJ32370","biotype":"protein_coding","ncbi_id":"137695","summary":null,"start":55696424,"end":55773407,"strand":-1,"description":"transmembrane protein 68 [Source:HGNC Symbol;Acc:HGNC:26510]"}, {"versioned_ensembl_gene_id":"ENSG00000260003.1","gene_symbol":"AC018767.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8276263,"end":8295700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204802.3","gene_symbol":"AL590399.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62374128,"end":62376836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220130.1","gene_symbol":"AL079342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89001548,"end":89001814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281263.1","gene_symbol":"AC136352.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21342227,"end":21344014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280277.1","gene_symbol":"AL079342.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88964527,"end":88966587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174370.9","gene_symbol":"C11orf45","gene_name":"chromosome 11 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:28584]","synonyms":"MGC35558,FLJ43646","biotype":"protein_coding","ncbi_id":"219833","summary":null,"start":128899565,"end":128906035,"strand":-1,"description":"chromosome 11 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:28584]"}, {"versioned_ensembl_gene_id":"ENSG00000249490.1","gene_symbol":"LINC02146","gene_name":"long intergenic non-protein coding RNA 2146 [Source:HGNC Symbol;Acc:HGNC:53006]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374677","summary":null,"start":20612625,"end":20614765,"strand":-1,"description":"long intergenic non-protein coding RNA 2146 [Source:HGNC Symbol;Acc:HGNC:53006]"}, {"versioned_ensembl_gene_id":"ENSG00000270136.5","gene_symbol":"MINOS1-NBL1","gene_name":"MINOS1-NBL1 readthrough [Source:HGNC Symbol;Acc:HGNC:48338]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532736","summary":"This locus represents naturally occurring read-through transcription between the neighboring chromosome 1 open reading frame 151 (GeneID 440574) and neuroblastoma suppressor of tumorigenicity 1 (GeneID 4681) genes on chromosome 1. The read-through transcripts produce at least two proteins, each of which share identity with proteins translated from the downstream neuroblastoma suppressor of tumorigenicity 1 locus. [provided by RefSeq, Feb 2011]","start":19596979,"end":19658056,"strand":1,"description":"MINOS1-NBL1 readthrough [Source:HGNC Symbol;Acc:HGNC:48338]"}, {"versioned_ensembl_gene_id":"ENSG00000164307.12","gene_symbol":"ERAP1","gene_name":"endoplasmic reticulum aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:18173]","synonyms":"PILS-AP,KIAA0525,ERAAP1,ARTS-1,A-LAP","biotype":"protein_coding","ncbi_id":"51752","summary":"The protein encoded by this gene is an aminopeptidase involved in trimming HLA class I-binding precursors so that they can be presented on MHC class I molecules. The encoded protein acts as a monomer or as a heterodimer with ERAP2. This protein may also be involved in blood pressure regulation by inactivation of angiotensin II. Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Oct 2010]","start":96760810,"end":96808100,"strand":-1,"description":"endoplasmic reticulum aminopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:18173]"}, {"versioned_ensembl_gene_id":"ENSG00000144029.11","gene_symbol":"MRPS5","gene_name":"mitochondrial ribosomal protein S5 [Source:HGNC Symbol;Acc:HGNC:14498]","synonyms":"S5mt,MRP-S5","biotype":"protein_coding","ncbi_id":"64969","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S5P family. Pseudogenes corresponding to this gene are found on chromosomes 4q, 5q, and 18q. [provided by RefSeq, Jul 2008]","start":95087207,"end":95149434,"strand":-1,"description":"mitochondrial ribosomal protein S5 [Source:HGNC Symbol;Acc:HGNC:14498]"}, {"versioned_ensembl_gene_id":"ENSG00000229808.1","gene_symbol":"AL391825.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":161890833,"end":161892196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118729.11","gene_symbol":"CASQ2","gene_name":"calsequestrin 2 [Source:HGNC Symbol;Acc:HGNC:1513]","synonyms":"PDIB2","biotype":"protein_coding","ncbi_id":"845","summary":"The protein encoded by this gene specifies the cardiac muscle family member of the calsequestrin family. Calsequestrin is localized to the sarcoplasmic reticulum in cardiac and slow skeletal muscle cells. The protein is a calcium binding protein that stores calcium for muscle function. Mutations in this gene cause stress-induced polymorphic ventricular tachycardia, also referred to as catecholaminergic polymorphic ventricular tachycardia 2 (CPVT2), a disease characterized by bidirectional ventricular tachycardia that may lead to cardiac arrest. [provided by RefSeq, Jul 2008]","start":115700007,"end":115768781,"strand":-1,"description":"calsequestrin 2 [Source:HGNC Symbol;Acc:HGNC:1513]"}, {"versioned_ensembl_gene_id":"ENSG00000114416.17","gene_symbol":"FXR1","gene_name":"FMR1 autosomal homolog 1 [Source:HGNC Symbol;Acc:HGNC:4023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8087","summary":"The protein encoded by this gene is an RNA binding protein that interacts with the functionally-similar proteins FMR1 and FXR2. These proteins shuttle between the nucleus and cytoplasm and associate with polyribosomes, predominantly with the 60S ribosomal subunit. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":180868141,"end":180982753,"strand":1,"description":"FMR1 autosomal homolog 1 [Source:HGNC Symbol;Acc:HGNC:4023]"}, {"versioned_ensembl_gene_id":"ENSG00000218772.2","gene_symbol":"FAM8A6P","gene_name":"family with sequence similarity 8 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:16377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"114182","summary":null,"start":134603564,"end":134604698,"strand":-1,"description":"family with sequence similarity 8 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:16377]"}, {"versioned_ensembl_gene_id":"ENSG00000255836.1","gene_symbol":"AC131206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7438780,"end":7439990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251665.1","gene_symbol":"AC005920.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50944104,"end":50948750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278437.4","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR-8,CD85c,LIR8","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54251016,"end":54257914,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000247011.2","gene_symbol":"AC005920.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50934989,"end":50944713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229722.1","gene_symbol":"AL078590.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134606299,"end":134609437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228596.1","gene_symbol":"AC013436.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44785050,"end":44787340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213113.3","gene_symbol":"TUBB8P8","gene_name":"tubulin beta 8 class VIII pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42346]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723626","summary":null,"start":198119721,"end":198120778,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42346]"}, {"versioned_ensembl_gene_id":"ENSG00000282311.1","gene_symbol":"AL133373.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91554410,"end":91554503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255369.1","gene_symbol":"AP000920.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128880325,"end":128880668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126883.16","gene_symbol":"NUP214","gene_name":"nucleoporin 214 [Source:HGNC Symbol;Acc:HGNC:8064]","synonyms":"N214,D9S46E,CAN,CAIN","biotype":"protein_coding","ncbi_id":"8021","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. This gene is a member of the FG-repeat-containing nucleoporins. The protein encoded by this gene is localized to the cytoplasmic face of the nuclear pore complex where it is required for proper cell cycle progression and nucleocytoplasmic transport. The 3' portion of this gene forms a fusion gene with the DEK gene on chromosome 6 in a t(6,9) translocation associated with acute myeloid leukemia and myelodysplastic syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":131125561,"end":131234670,"strand":1,"description":"nucleoporin 214 [Source:HGNC Symbol;Acc:HGNC:8064]"}, {"versioned_ensembl_gene_id":"ENSG00000236246.2","gene_symbol":"AC073135.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":198121479,"end":198123232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231212.1","gene_symbol":"AL590399.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62349941,"end":62351536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141497.13","gene_symbol":"ZMYND15","gene_name":"zinc finger MYND-type containing 15 [Source:HGNC Symbol;Acc:HGNC:20997]","synonyms":"DKFZp434N127","biotype":"protein_coding","ncbi_id":"84225","summary":"This gene encodes a MYND-containing zinc-binding protein with a nuclear localization sequence. A similar gene in mice has been shown to act as a testis-specific transcriptional repressor by recruiting histone deacetylase enzymes to regulate spatiotemporal expression of many haploid genes. This protein may play an important role in spermatogenesis. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]","start":4740015,"end":4746119,"strand":1,"description":"zinc finger MYND-type containing 15 [Source:HGNC Symbol;Acc:HGNC:20997]"}, {"versioned_ensembl_gene_id":"ENSG00000261176.1","gene_symbol":"AC009117.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82554049,"end":82575210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119878.5","gene_symbol":"CRIPT","gene_name":"CXXC repeat containing interactor of PDZ3 domain [Source:HGNC Symbol;Acc:HGNC:14312]","synonyms":"HSPC139","biotype":"protein_coding","ncbi_id":"9419","summary":"This gene encodes a protein that binds to the PDZ3 peptide recognition domain. The encoded protein may modulates protein interactions with the cytoskeleton. A mutation in this gene resulted in short stature with microcephaly and distinctive facies. [provided by RefSeq, Jun 2014]","start":46616416,"end":46625742,"strand":1,"description":"CXXC repeat containing interactor of PDZ3 domain [Source:HGNC Symbol;Acc:HGNC:14312]"}, {"versioned_ensembl_gene_id":"ENSG00000228425.9","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"SACM2L,ARE1","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33228191,"end":33249968,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000280633.2","gene_symbol":"AL133373.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91572444,"end":91575271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236450.1","gene_symbol":"AL590399.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62357834,"end":62358140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284702.1","gene_symbol":"AL136115.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31972189,"end":31987034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283446.1","gene_symbol":"Z99571.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85143427,"end":85156444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279608.1","gene_symbol":"AL353795.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35038625,"end":35044326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174038.12","gene_symbol":"C9orf131","gene_name":"chromosome 9 open reading frame 131 [Source:HGNC Symbol;Acc:HGNC:31418]","synonyms":"MGC41945","biotype":"protein_coding","ncbi_id":"138724","summary":null,"start":35041095,"end":35045991,"strand":1,"description":"chromosome 9 open reading frame 131 [Source:HGNC Symbol;Acc:HGNC:31418]"}, {"versioned_ensembl_gene_id":"ENSG00000155367.15","gene_symbol":"PPM1J","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1J [Source:HGNC Symbol;Acc:HGNC:20785]","synonyms":"PPP2CZ,PP2Czeta,MGC19531,FLJ35951,DKFZp434P1514","biotype":"protein_coding","ncbi_id":"333926","summary":"This gene encodes the serine/threonine protein phosphatase. The mouse homolog of this gene apparently belongs to the protein phosphatase 2C family of genes. The exact function of this gene is not yet known. [provided by RefSeq, Jul 2008]","start":112709994,"end":112715477,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1J [Source:HGNC Symbol;Acc:HGNC:20785]"}, {"versioned_ensembl_gene_id":"ENSG00000072803.17","gene_symbol":"FBXW11","gene_name":"F-box and WD repeat domain containing 11 [Source:HGNC Symbol;Acc:HGNC:13607]","synonyms":"Fbw11,BTRCP2,BTRC2,KIAA0696,Hos,FBXW1B,Fbw1b","biotype":"protein_coding","ncbi_id":"23291","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbws class and, in addition to an F-box, contains multiple WD40 repeats. This gene contains at least 14 exons, and its alternative splicing generates 3 transcript variants diverging at the presence/absence of two alternate exons. [provided by RefSeq, Jul 2008]","start":171861549,"end":172006873,"strand":-1,"description":"F-box and WD repeat domain containing 11 [Source:HGNC Symbol;Acc:HGNC:13607]"}, {"versioned_ensembl_gene_id":"ENSG00000111880.15","gene_symbol":"RNGTT","gene_name":"RNA guanylyltransferase and 5'-phosphatase [Source:HGNC Symbol;Acc:HGNC:10073]","synonyms":"HCE,hCAP,HCE1","biotype":"protein_coding","ncbi_id":"8732","summary":null,"start":88610272,"end":88963721,"strand":-1,"description":"RNA guanylyltransferase and 5'-phosphatase [Source:HGNC Symbol;Acc:HGNC:10073]"}, {"versioned_ensembl_gene_id":"ENSG00000206449.11","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31488393,"end":31501409,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000205702.10","gene_symbol":"CYP2D7","gene_name":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]","synonyms":"CYP2D7P1,CYP2D7P,CYP2D,CYP2D@","biotype":"polymorphic_pseudogene","ncbi_id":"1564","summary":"This gene is a member of the cytochrome P450 gene superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is a segregating pseudogene, where some individuals may have an allele that encodes a functional enzyme, while other individuals have an allele encoding a protein that is predicted to be non-functional. In this case, the functional allele is thought to be rare. This locus is part of a cluster of cytochrome P450 genes on chromosome 22. [provided by RefSeq, Jan 2017]","start":42140203,"end":42144577,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]"}, {"versioned_ensembl_gene_id":"ENSG00000227560.1","gene_symbol":"RPS15AP30","gene_name":"ribosomal protein S15a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35495]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271607","summary":null,"start":112987476,"end":112987865,"strand":1,"description":"ribosomal protein S15a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35495]"}, {"versioned_ensembl_gene_id":"ENSG00000233547.1","gene_symbol":"AL158212.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112950646,"end":112951875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259121.2","gene_symbol":"AL109628.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39090901,"end":39091101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263001.5","gene_symbol":"GTF2I","gene_name":"general transcription factor IIi [Source:HGNC Symbol;Acc:HGNC:4659]","synonyms":"WBSCR6,TFII-I,SPIN,IB291,DIWS,BTKAP1,BAP-135","biotype":"protein_coding","ncbi_id":"2969","summary":"This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013]","start":74657667,"end":74760692,"strand":1,"description":"general transcription factor IIi [Source:HGNC Symbol;Acc:HGNC:4659]"}, {"versioned_ensembl_gene_id":"ENSG00000258591.2","gene_symbol":"AL109628.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39108342,"end":39108707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276935.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173818,"end":54190312,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000100934.14","gene_symbol":"SEC23A","gene_name":"Sec23 homolog A, coat complex II component [Source:HGNC Symbol;Acc:HGNC:10701]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10484","summary":"The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family. It is part of a protein complex and found in the ribosome-free transitional face of the endoplasmic reticulum (ER) and associated vesicles. This protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The encoded protein is suggested to play a role in the ER-Golgi protein trafficking. [provided by RefSeq, Jul 2008]","start":39031919,"end":39109646,"strand":-1,"description":"Sec23 homolog A, coat complex II component [Source:HGNC Symbol;Acc:HGNC:10701]"}, {"versioned_ensembl_gene_id":"ENSG00000261029.1","gene_symbol":"AC138304.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82170296,"end":82175803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255514.1","gene_symbol":"OR4B2P","gene_name":"olfactory receptor family 4 subfamily B member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8291]","synonyms":"hg449","biotype":"unprocessed_pseudogene","ncbi_id":"26690","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48227429,"end":48228310,"strand":1,"description":"olfactory receptor family 4 subfamily B member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8291]"}, {"versioned_ensembl_gene_id":"ENSG00000144026.11","gene_symbol":"ZNF514","gene_name":"zinc finger protein 514 [Source:HGNC Symbol;Acc:HGNC:25894]","synonyms":"FLJ14457","biotype":"protein_coding","ncbi_id":"84874","summary":null,"start":95147330,"end":95165413,"strand":-1,"description":"zinc finger protein 514 [Source:HGNC Symbol;Acc:HGNC:25894]"}, {"versioned_ensembl_gene_id":"ENSG00000169413.2","gene_symbol":"RNASE6","gene_name":"ribonuclease A family member k6 [Source:HGNC Symbol;Acc:HGNC:10048]","synonyms":"RNS6,RNaseK6,RAD1","biotype":"protein_coding","ncbi_id":"6039","summary":"The protein encoded by this gene is a member of the ribonuclease A superfamily and functions in the urinary tract. The protein has broad-spectrum antimicrobial activity against pathogenic bacteria. [provided by RefSeq, Nov 2014]","start":20781051,"end":20782467,"strand":1,"description":"ribonuclease A family member k6 [Source:HGNC Symbol;Acc:HGNC:10048]"}, {"versioned_ensembl_gene_id":"ENSG00000272990.1","gene_symbol":"AC084036.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156523740,"end":156524247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242017.1","gene_symbol":"ALG1L15P","gene_name":"asparagine-linked glycosylation 1-like 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:44384]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730086","summary":null,"start":156044155,"end":156044948,"strand":-1,"description":"asparagine-linked glycosylation 1-like 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:44384]"}, {"versioned_ensembl_gene_id":"ENSG00000242537.1","gene_symbol":"MRE11P1","gene_name":"MRE11 homolog, double strand break repair nuclease pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7231]","synonyms":"MRE11B","biotype":"processed_pseudogene","ncbi_id":"4362","summary":null,"start":156111432,"end":156114198,"strand":-1,"description":"MRE11 homolog, double strand break repair nuclease pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7231]"}, {"versioned_ensembl_gene_id":"ENSG00000236269.1","gene_symbol":"ENO1-IT1","gene_name":"ENO1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41331]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480431","summary":null,"start":8875788,"end":8878007,"strand":-1,"description":"ENO1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41331]"}, {"versioned_ensembl_gene_id":"ENSG00000240596.1","gene_symbol":"KCNAB1-AS2","gene_name":"KCNAB1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40315]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874083","summary":null,"start":156215560,"end":156227883,"strand":-1,"description":"KCNAB1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40315]"}, {"versioned_ensembl_gene_id":"ENSG00000230679.1","gene_symbol":"ENO1-AS1","gene_name":"ENO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40214]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505975","summary":null,"start":8878835,"end":8879894,"strand":1,"description":"ENO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40214]"}, {"versioned_ensembl_gene_id":"ENSG00000247287.2","gene_symbol":"AL359220.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61298164,"end":61322818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172208.6","gene_symbol":"OR4X2","gene_name":"olfactory receptor family 4 subfamily X member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15184]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"119764","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":48245056,"end":48246080,"strand":1,"description":"olfactory receptor family 4 subfamily X member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15184]"}, {"versioned_ensembl_gene_id":"ENSG00000074800.13","gene_symbol":"ENO1","gene_name":"enolase 1 [Source:HGNC Symbol;Acc:HGNC:3350]","synonyms":"PPH,MPB1,MBP-1,ENO1L1","biotype":"protein_coding","ncbi_id":"2023","summary":"This gene encodes alpha-enolase, one of three enolase isoenzymes found in mammals. Each isoenzyme is a homodimer composed of 2 alpha, 2 gamma, or 2 beta subunits, and functions as a glycolytic enzyme. Alpha-enolase in addition, functions as a structural lens protein (tau-crystallin) in the monomeric form. Alternative splicing of this gene results in a shorter isoform that has been shown to bind to the c-myc promoter and function as a tumor suppressor. Several pseudogenes have been identified, including one on the long arm of chromosome 1. Alpha-enolase has also been identified as an autoantigen in Hashimoto encephalopathy. [provided by RefSeq, Jan 2011]","start":8861002,"end":8879249,"strand":-1,"description":"enolase 1 [Source:HGNC Symbol;Acc:HGNC:3350]"}, {"versioned_ensembl_gene_id":"ENSG00000119729.11","gene_symbol":"RHOQ","gene_name":"ras homolog family member Q [Source:HGNC Symbol;Acc:HGNC:17736]","synonyms":"TC10,RASL7A,ARHQ","biotype":"protein_coding","ncbi_id":"23433","summary":"This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. The encoded protein is an important signalling protein for sarcomere assembly and has been shown to play a significant role in the exocytosis of the solute carrier family 2, facilitated glucose transporter member 4 and other proteins, possibly acting as the signal that turns on the membrane fusion machinery. Three related pseudogene have been identified on chromosomes 2 and 14. [provided by RefSeq, Aug 2011]","start":46541806,"end":46583121,"strand":1,"description":"ras homolog family member Q [Source:HGNC Symbol;Acc:HGNC:17736]"}, {"versioned_ensembl_gene_id":"ENSG00000258810.1","gene_symbol":"AL133371.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20783888,"end":20784293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237306.1","gene_symbol":"HSPE1P22","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:49341]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289607","summary":null,"start":92027498,"end":92027824,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:49341]"}, {"versioned_ensembl_gene_id":"ENSG00000227008.2","gene_symbol":"AL009174.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133670971,"end":133671386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176567.1","gene_symbol":"OR4X1","gene_name":"olfactory receptor family 4 subfamily X member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14854]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390113","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":48263861,"end":48264778,"strand":1,"description":"olfactory receptor family 4 subfamily X member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14854]"}, {"versioned_ensembl_gene_id":"ENSG00000147257.13","gene_symbol":"GPC3","gene_name":"glypican 3 [Source:HGNC Symbol;Acc:HGNC:4451]","synonyms":"SGBS1,SGBS,SGB,SDYS,OCI-5,DGSX","biotype":"protein_coding","ncbi_id":"2719","summary":"Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":133535745,"end":133985895,"strand":-1,"description":"glypican 3 [Source:HGNC Symbol;Acc:HGNC:4451]"}, {"versioned_ensembl_gene_id":"ENSG00000087302.8","gene_symbol":"C14orf166","gene_name":"chromosome 14 open reading frame 166 [Source:HGNC Symbol;Acc:HGNC:23169]","synonyms":"RLLM1,LCRP369,hCLE1,CLE7,CLE,CGI-99","biotype":"protein_coding","ncbi_id":"51637","summary":null,"start":51989475,"end":52010691,"strand":1,"description":"chromosome 14 open reading frame 166 [Source:HGNC Symbol;Acc:HGNC:23169]"}, {"versioned_ensembl_gene_id":"ENSG00000272109.1","gene_symbol":"AC008906.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96804353,"end":96806105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155366.16","gene_symbol":"RHOC","gene_name":"ras homolog family member C [Source:HGNC Symbol;Acc:HGNC:669]","synonyms":"RhoC,ARHC,ARH9","biotype":"protein_coding","ncbi_id":"389","summary":"This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. The protein encoded by this gene is prenylated at its C-terminus, and localizes to the cytoplasm and plasma membrane. It is thought to be important in cell locomotion. Overexpression of this gene is associated with tumor cell proliferation and metastasis. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":112701106,"end":112707434,"strand":-1,"description":"ras homolog family member C [Source:HGNC Symbol;Acc:HGNC:669]"}, {"versioned_ensembl_gene_id":"ENSG00000251314.2","gene_symbol":"AC104123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95962001,"end":96631085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213232.2","gene_symbol":"PPP1R2P10","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128626","summary":null,"start":63811014,"end":63811608,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42008]"}, {"versioned_ensembl_gene_id":"ENSG00000175426.10","gene_symbol":"PCSK1","gene_name":"proprotein convertase subtilisin/kexin type 1 [Source:HGNC Symbol;Acc:HGNC:8743]","synonyms":"NEC1,SPC3,PC3,PC1","biotype":"protein_coding","ncbi_id":"5122","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to subcellular compartments where a second autocatalytic even takes place and the catalytic activity is acquired. The protease is packaged into and activated in dense core secretory granules and expressed in the neuroendocrine system and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It functions in the proteolytic activation of polypeptide hormones and neuropeptides precursors. Mutations in this gene have been associated with susceptibility to obesity and proprotein convertase 1/3 deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene [provided by RefSeq, Jan 2014]","start":96390415,"end":96434143,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 1 [Source:HGNC Symbol;Acc:HGNC:8743]"}, {"versioned_ensembl_gene_id":"ENSG00000153404.14","gene_symbol":"PLEKHG4B","gene_name":"pleckstrin homology and RhoGEF domain containing G4B [Source:HGNC Symbol;Acc:HGNC:29399]","synonyms":"KIAA1909","biotype":"protein_coding","ncbi_id":"153478","summary":"This gene encodes a large protein that contains a pleckstrin homology domain and may function as a guanine nucleotide exchange factor. [provided by RefSeq, May 2017]","start":92151,"end":189972,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G4B [Source:HGNC Symbol;Acc:HGNC:29399]"}, {"versioned_ensembl_gene_id":"ENSG00000257923.9","gene_symbol":"CUX1","gene_name":"cut like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:2557]","synonyms":"CDP,CASP,GOLIM6,Cux/CDP,CUX,CUTL1,CUT,Clox,CDP1,CDP/Cux,CDP/Cut","biotype":"protein_coding","ncbi_id":"1523","summary":"The protein encoded by this gene is a member of the homeodomain family of DNA binding proteins. It may regulate gene expression, morphogenesis, and differentiation and it may also play a role in the cell cycle progession. Several alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Feb 2011]","start":101815904,"end":102283957,"strand":1,"description":"cut like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:2557]"}, {"versioned_ensembl_gene_id":"ENSG00000233654.1","gene_symbol":"AC108047.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":190534855,"end":190568102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176900.2","gene_symbol":"OR51T1","gene_name":"olfactory receptor family 51 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:15205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401665","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4881819,"end":4882883,"strand":1,"description":"olfactory receptor family 51 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:15205]"}, {"versioned_ensembl_gene_id":"ENSG00000173726.10","gene_symbol":"TOMM20","gene_name":"translocase of outer mitochondrial membrane 20 [Source:HGNC Symbol;Acc:HGNC:20947]","synonyms":"TOM20,MOM19,MAS20,KIAA0016","biotype":"protein_coding","ncbi_id":"9804","summary":null,"start":235109336,"end":235128936,"strand":-1,"description":"translocase of outer mitochondrial membrane 20 [Source:HGNC Symbol;Acc:HGNC:20947]"}, {"versioned_ensembl_gene_id":"ENSG00000205497.4","gene_symbol":"OR51A4","gene_name":"olfactory receptor family 51 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14795]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401666","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4942831,"end":4947605,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:14795]"}, {"versioned_ensembl_gene_id":"ENSG00000185924.6","gene_symbol":"RTN4RL1","gene_name":"reticulon 4 receptor like 1 [Source:HGNC Symbol;Acc:HGNC:21329]","synonyms":"NGRH2,NgR3,DKFZp547J144","biotype":"protein_coding","ncbi_id":"146760","summary":null,"start":1934677,"end":2025345,"strand":-1,"description":"reticulon 4 receptor like 1 [Source:HGNC Symbol;Acc:HGNC:21329]"}, {"versioned_ensembl_gene_id":"ENSG00000262869.1","gene_symbol":"AC099684.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2019952,"end":2023664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228133.2","gene_symbol":"AC099684.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2017716,"end":2020706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233143.1","gene_symbol":"DIRC3-AS1","gene_name":"DIRC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50636]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373877","summary":null,"start":217282739,"end":217336120,"strand":1,"description":"DIRC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50636]"}, {"versioned_ensembl_gene_id":"ENSG00000205496.1","gene_symbol":"OR51A2","gene_name":"olfactory receptor family 51 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:14764]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401667","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4954772,"end":4955713,"strand":-1,"description":"olfactory receptor family 51 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:14764]"}, {"versioned_ensembl_gene_id":"ENSG00000203667.9","gene_symbol":"COX20","gene_name":"COX20, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:26970]","synonyms":"FLJ43269,FAM36A","biotype":"protein_coding","ncbi_id":"116228","summary":"This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":244835322,"end":244845057,"strand":1,"description":"COX20, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:26970]"}, {"versioned_ensembl_gene_id":"ENSG00000164088.17","gene_symbol":"PPM1M","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1M [Source:HGNC Symbol;Acc:HGNC:26506]","synonyms":"PP2Ceta,FLJ32332","biotype":"protein_coding","ncbi_id":"132160","summary":null,"start":52245793,"end":52250597,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1M [Source:HGNC Symbol;Acc:HGNC:26506]"}, {"versioned_ensembl_gene_id":"ENSG00000249158.6","gene_symbol":"PCDHA11","gene_name":"protocadherin alpha 11 [Source:HGNC Symbol;Acc:HGNC:8665]","synonyms":"PCDH-ALPHA11,CRNR7,CNRS7,CNRN7,CNR7","biotype":"protein_coding","ncbi_id":"56138","summary":"This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":140868183,"end":141012344,"strand":1,"description":"protocadherin alpha 11 [Source:HGNC Symbol;Acc:HGNC:8665]"}, {"versioned_ensembl_gene_id":"ENSG00000278839.4","gene_symbol":"SERF1B","gene_name":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]","synonyms":"H4F5C,FAM2B","biotype":"protein_coding","ncbi_id":"728492","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008]","start":69709074,"end":69726961,"strand":-1,"description":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]"}, {"versioned_ensembl_gene_id":"ENSG00000170236.14","gene_symbol":"USP50","gene_name":"ubiquitin specific peptidase 50 [Source:HGNC Symbol;Acc:HGNC:20079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"373509","summary":null,"start":50500562,"end":50546708,"strand":-1,"description":"ubiquitin specific peptidase 50 [Source:HGNC Symbol;Acc:HGNC:20079]"}, {"versioned_ensembl_gene_id":"ENSG00000264860.1","gene_symbol":"AC097641.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73164977,"end":73196593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267265.5","gene_symbol":"AC011476.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55006193,"end":55048086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129084.17","gene_symbol":"PSMA1","gene_name":"proteasome subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:9530]","synonyms":"PROS30,NU,MGC23915,MGC22853,MGC21459,MGC1667,MGC14751,MGC14575,MGC14542,HC2","biotype":"protein_coding","ncbi_id":"5682","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jan 2009]","start":14504874,"end":14643635,"strand":-1,"description":"proteasome subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:9530]"}, {"versioned_ensembl_gene_id":"ENSG00000182732.16","gene_symbol":"RGS6","gene_name":"regulator of G protein signaling 6 [Source:HGNC Symbol;Acc:HGNC:10002]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9628","summary":"This gene encodes a member of the RGS (regulator of G protein signaling) family of proteins, which are defined by the presence of a RGS domain that confers the GTPase-activating activity of these proteins toward certain G alpha subunits. This protein also belongs to a subfamily of RGS proteins characterized by the presence of DEP and GGL domains, the latter a G beta 5-interacting domain. The RGS proteins negatively regulate G protein signaling, and may modulate neuronal, cardiovascular, lymphocytic activities, and cancer risk. Many alternatively spliced transcript variants encoding different isoforms with long or short N-terminal domains, complete or incomplete GGL domains, and distinct C-terminal domains, have been described for this gene, however, the full-length nature of some of these variants is not known.[provided by RefSeq, Mar 2011]","start":71932439,"end":72566529,"strand":1,"description":"regulator of G protein signaling 6 [Source:HGNC Symbol;Acc:HGNC:10002]"}, {"versioned_ensembl_gene_id":"ENSG00000108256.8","gene_symbol":"NUFIP2","gene_name":"NUFIP2, FMR1 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17634]","synonyms":"PIG1,MGC117262,KIAA1321,FIP-82,82-FIP,182-FIP","biotype":"protein_coding","ncbi_id":"57532","summary":null,"start":29255836,"end":29294118,"strand":-1,"description":"NUFIP2, FMR1 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:17634]"}, {"versioned_ensembl_gene_id":"ENSG00000180535.3","gene_symbol":"BHLHA15","gene_name":"basic helix-loop-helix family member a15 [Source:HGNC Symbol;Acc:HGNC:22265]","synonyms":"MIST1,BHLHB8,bHLHa15","biotype":"protein_coding","ncbi_id":"168620","summary":null,"start":98211427,"end":98212979,"strand":1,"description":"basic helix-loop-helix family member a15 [Source:HGNC Symbol;Acc:HGNC:22265]"}, {"versioned_ensembl_gene_id":"ENSG00000169727.12","gene_symbol":"GPS1","gene_name":"G protein pathway suppressor 1 [Source:HGNC Symbol;Acc:HGNC:4549]","synonyms":"CSN1,COPS1","biotype":"protein_coding","ncbi_id":"2873","summary":"This gene is known to suppress G-protein and mitogen-activated signal transduction in mammalian cells. The encoded protein shares significant similarity with Arabidopsis FUS6, which is a regulator of light-mediated signal transduction in plant cells. [provided by RefSeq, Mar 2016]","start":82050691,"end":82057470,"strand":1,"description":"G protein pathway suppressor 1 [Source:HGNC Symbol;Acc:HGNC:4549]"}, {"versioned_ensembl_gene_id":"ENSG00000232268.6","gene_symbol":"OR52I1","gene_name":"olfactory receptor family 52 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15220]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390037","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4593614,"end":4596574,"strand":1,"description":"olfactory receptor family 52 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:15220]"}, {"versioned_ensembl_gene_id":"ENSG00000258867.5","gene_symbol":"LINC01146","gene_name":"long intergenic non-protein coding RNA 1146 [Source:HGNC Symbol;Acc:HGNC:49467]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283587","summary":null,"start":88024550,"end":88097619,"strand":1,"description":"long intergenic non-protein coding RNA 1146 [Source:HGNC Symbol;Acc:HGNC:49467]"}, {"versioned_ensembl_gene_id":"ENSG00000271018.1","gene_symbol":"AC013244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50756892,"end":50757433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171680.21","gene_symbol":"PLEKHG5","gene_name":"pleckstrin homology and RhoGEF domain containing G5 [Source:HGNC Symbol;Acc:HGNC:29105]","synonyms":"Tech,Syx,KIAA0720,GEF720","biotype":"protein_coding","ncbi_id":"57449","summary":"This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":6466092,"end":6520061,"strand":-1,"description":"pleckstrin homology and RhoGEF domain containing G5 [Source:HGNC Symbol;Acc:HGNC:29105]"}, {"versioned_ensembl_gene_id":"ENSG00000250613.1","gene_symbol":"AC110768.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10410996,"end":10411644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225377.5","gene_symbol":"NRSN2-AS1","gene_name":"NRSN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51222]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507459","summary":null,"start":320313,"end":348224,"strand":-1,"description":"NRSN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51222]"}, {"versioned_ensembl_gene_id":"ENSG00000228225.1","gene_symbol":"AC016908.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84031140,"end":84032358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259465.2","gene_symbol":"AHCYP7","gene_name":"adenosylhomocysteinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44999]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645486","summary":null,"start":50417385,"end":50418692,"strand":1,"description":"adenosylhomocysteinase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44999]"}, {"versioned_ensembl_gene_id":"ENSG00000173611.17","gene_symbol":"SCAI","gene_name":"suppressor of cancer cell invasion [Source:HGNC Symbol;Acc:HGNC:26709]","synonyms":"NET40,FLJ36664,C9orf126","biotype":"protein_coding","ncbi_id":"286205","summary":"This gene encodes a regulator of cell migration. The encoded protein appears to function in the RhoA (ras homolog gene family, member A)-Dia1 (diaphanous homolog 1) signal transduction pathway. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]","start":124942608,"end":125143506,"strand":-1,"description":"suppressor of cancer cell invasion [Source:HGNC Symbol;Acc:HGNC:26709]"}, {"versioned_ensembl_gene_id":"ENSG00000230945.1","gene_symbol":"LINC01507","gene_name":"long intergenic non-protein coding RNA 1507 [Source:HGNC Symbol;Acc:HGNC:51189]","synonyms":"XLOC_000303","biotype":"lincRNA","ncbi_id":"101927477","summary":null,"start":80030579,"end":80034555,"strand":1,"description":"long intergenic non-protein coding RNA 1507 [Source:HGNC Symbol;Acc:HGNC:51189]"}, {"versioned_ensembl_gene_id":"ENSG00000235575.1","gene_symbol":"Z99758.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169310665,"end":169322479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259285.1","gene_symbol":"AC025431.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58065225,"end":58071043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237498.2","gene_symbol":"AC010105.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82479128,"end":82538711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254574.1","gene_symbol":"AC105219.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143709007,"end":143713584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278175.3","gene_symbol":"GLIDR","gene_name":"glioblastoma down-regulated RNA [Source:HGNC Symbol;Acc:HGNC:48823]","synonyms":"TCONS_00015562,MGC21881,LINC01172","biotype":"lincRNA","ncbi_id":"389741","summary":null,"start":39748514,"end":39810097,"strand":-1,"description":"glioblastoma down-regulated RNA [Source:HGNC Symbol;Acc:HGNC:48823]"}, {"versioned_ensembl_gene_id":"ENSG00000135052.16","gene_symbol":"GOLM1","gene_name":"golgi membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:15451]","synonyms":"GP73,GOLPH2,FLJ23608,C9orf155,bA379P1.3","biotype":"protein_coding","ncbi_id":"51280","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a type II Golgi transmembrane protein. It processes proteins synthesized in the rough endoplasmic reticulum and assists in the transport of protein cargo through the Golgi apparatus. The expression of this gene has been observed to be upregulated in response to viral infection. Alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Sep 2009]","start":86026146,"end":86100173,"strand":-1,"description":"golgi membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:15451]"}, {"versioned_ensembl_gene_id":"ENSG00000255663.1","gene_symbol":"AP002373.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":114400682,"end":114443932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237056.5","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"BING1,ZBTB22A,fruitless,ZNF297A,fru,ZNF297","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33484759,"end":33488283,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000267009.6","gene_symbol":"AC007780.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":68413623,"end":68524949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240849.10","gene_symbol":"TMEM189","gene_name":"transmembrane protein 189 [Source:HGNC Symbol;Acc:HGNC:16735]","synonyms":"Kua","biotype":"protein_coding","ncbi_id":"387521","summary":"Co-transcription of this gene and the neighboring downstream gene (ubiquitin-conjugating enzyme E2 variant 1) generates a rare read-through transcript, which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. The protein encoded by this individual gene lacks a UEV1 domain but includes three transmembrane regions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]","start":50118254,"end":50153734,"strand":-1,"description":"transmembrane protein 189 [Source:HGNC Symbol;Acc:HGNC:16735]"}, {"versioned_ensembl_gene_id":"ENSG00000258052.1","gene_symbol":"AC025263.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69801669,"end":69855363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073050.11","gene_symbol":"XRCC1","gene_name":"X-ray repair cross complementing 1 [Source:HGNC Symbol;Acc:HGNC:12828]","synonyms":"RCC","biotype":"protein_coding","ncbi_id":"7515","summary":"The protein encoded by this gene is involved in the efficient repair of DNA single-strand breaks formed by exposure to ionizing radiation and alkylating agents. This protein interacts with DNA ligase III, polymerase beta and poly (ADP-ribose) polymerase to participate in the base excision repair pathway. It may play a role in DNA processing during meiogenesis and recombination in germ cells. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008]","start":43543040,"end":43580473,"strand":-1,"description":"X-ray repair cross complementing 1 [Source:HGNC Symbol;Acc:HGNC:12828]"}, {"versioned_ensembl_gene_id":"ENSG00000239490.1","gene_symbol":"RPS4XP18","gene_name":"ribosomal protein S4X pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36170]","synonyms":"RPS4P18","biotype":"processed_pseudogene","ncbi_id":"646583","summary":null,"start":22586465,"end":22587227,"strand":1,"description":"ribosomal protein S4X pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36170]"}, {"versioned_ensembl_gene_id":"ENSG00000143674.10","gene_symbol":"MAP3K21","gene_name":"mitogen-activated protein kinase kinase kinase 21 [Source:HGNC Symbol;Acc:HGNC:29798]","synonyms":"MLK4,KIAA1804","biotype":"protein_coding","ncbi_id":"84451","summary":null,"start":233327768,"end":233385148,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 21 [Source:HGNC Symbol;Acc:HGNC:29798]"}, {"versioned_ensembl_gene_id":"ENSG00000272650.1","gene_symbol":"AC110792.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53997415,"end":53997712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226813.2","gene_symbol":"LINC01941","gene_name":"long intergenic non-protein coding RNA 1941 [Source:HGNC Symbol;Acc:HGNC:52764]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373600","summary":null,"start":126110099,"end":126117985,"strand":-1,"description":"long intergenic non-protein coding RNA 1941 [Source:HGNC Symbol;Acc:HGNC:52764]"}, {"versioned_ensembl_gene_id":"ENSG00000255411.1","gene_symbol":"LINC02548","gene_name":"long intergenic non-protein coding RNA 2548 [Source:HGNC Symbol;Acc:HGNC:53583]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376562","summary":null,"start":13785390,"end":13848002,"strand":1,"description":"long intergenic non-protein coding RNA 2548 [Source:HGNC Symbol;Acc:HGNC:53583]"}, {"versioned_ensembl_gene_id":"ENSG00000175003.12","gene_symbol":"SLC22A1","gene_name":"solute carrier family 22 member 1 [Source:HGNC Symbol;Acc:HGNC:10963]","synonyms":"OCT1","biotype":"protein_coding","ncbi_id":"6580","summary":"Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter. [provided by RefSeq, Jul 2008]","start":160121789,"end":160158718,"strand":1,"description":"solute carrier family 22 member 1 [Source:HGNC Symbol;Acc:HGNC:10963]"}, {"versioned_ensembl_gene_id":"ENSG00000255506.1","gene_symbol":"AP003718.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92748732,"end":92766867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256614.1","gene_symbol":"AK6P1","gene_name":"adenylate kinase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51678]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132086","summary":null,"start":34249481,"end":34249958,"strand":1,"description":"adenylate kinase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51678]"}, {"versioned_ensembl_gene_id":"ENSG00000233444.1","gene_symbol":"AC013262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81666477,"end":81666728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231741.2","gene_symbol":"AL353743.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85934588,"end":85936599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165121.11","gene_symbol":"AL353743.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85805359,"end":85849542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128731.15","gene_symbol":"HERC2","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]","synonyms":"p528,jdf2,D15F37S1","biotype":"protein_coding","ncbi_id":"8924","summary":"This gene belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16. [provided by RefSeq, Mar 2012]","start":28111040,"end":28322152,"strand":-1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]"}, {"versioned_ensembl_gene_id":"ENSG00000165323.15","gene_symbol":"FAT3","gene_name":"FAT atypical cadherin 3 [Source:HGNC Symbol;Acc:HGNC:23112]","synonyms":"KIAA1989,CDHR10,CDHF15","biotype":"protein_coding","ncbi_id":"120114","summary":null,"start":92352096,"end":92896470,"strand":1,"description":"FAT atypical cadherin 3 [Source:HGNC Symbol;Acc:HGNC:23112]"}, {"versioned_ensembl_gene_id":"ENSG00000278329.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRZ,KIR15,KIR2DL6,KIRY","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754958,"end":54767306,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000248710.1","gene_symbol":"AC079594.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":160227454,"end":160449829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185585.19","gene_symbol":"OLFML2A","gene_name":"olfactomedin like 2A [Source:HGNC Symbol;Acc:HGNC:27270]","synonyms":"FLJ00237","biotype":"protein_coding","ncbi_id":"169611","summary":null,"start":124777158,"end":124814885,"strand":1,"description":"olfactomedin like 2A [Source:HGNC Symbol;Acc:HGNC:27270]"}, {"versioned_ensembl_gene_id":"ENSG00000260423.1","gene_symbol":"LINC02367","gene_name":"long intergenic non-protein coding RNA 2367 [Source:HGNC Symbol;Acc:HGNC:53290]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101930452","summary":null,"start":9367464,"end":9397617,"strand":1,"description":"long intergenic non-protein coding RNA 2367 [Source:HGNC Symbol;Acc:HGNC:53290]"}, {"versioned_ensembl_gene_id":"ENSG00000167916.4","gene_symbol":"KRT24","gene_name":"keratin 24 [Source:HGNC Symbol;Acc:HGNC:18527]","synonyms":"MGC138173,MGC138169,FLJ20261","biotype":"protein_coding","ncbi_id":"192666","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jun 2009]","start":40697991,"end":40703750,"strand":-1,"description":"keratin 24 [Source:HGNC Symbol;Acc:HGNC:18527]"}, {"versioned_ensembl_gene_id":"ENSG00000235547.3","gene_symbol":"NDUFB11P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33980]","synonyms":"NDUFB11P","biotype":"processed_pseudogene","ncbi_id":"390239","summary":null,"start":92336032,"end":92336496,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33980]"}, {"versioned_ensembl_gene_id":"ENSG00000122852.14","gene_symbol":"SFTPA1","gene_name":"surfactant protein A1 [Source:HGNC Symbol;Acc:HGNC:10798]","synonyms":"SP-A1,SP-A,SFTP1,COLEC4","biotype":"protein_coding","ncbi_id":"653509","summary":"This gene encodes a lung surfactant protein that is a member of a subfamily of C-type lectins called collectins. The encoded protein binds specific carbohydrate moieties found on lipids and on the surface of microorganisms. This protein plays an essential role in surfactant homeostasis and in the defense against respiratory pathogens. Mutations in this gene are associated with idiopathic pulmonary fibrosis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":79610939,"end":79615455,"strand":1,"description":"surfactant protein A1 [Source:HGNC Symbol;Acc:HGNC:10798]"}, {"versioned_ensembl_gene_id":"ENSG00000272622.1","gene_symbol":"AC010735.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":226800146,"end":226811029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174483.19","gene_symbol":"BBS1","gene_name":"Bardet-Biedl syndrome 1 [Source:HGNC Symbol;Acc:HGNC:966]","synonyms":"FLJ23590","biotype":"protein_coding","ncbi_id":"582","summary":"Mutations in this gene have been observed in patients with the major form (type 1) of Bardet-Biedl syndrome. The encoded protein may play a role in eye, limb, cardiac and reproductive system development. [provided by RefSeq, Jul 2008]","start":66510606,"end":66533627,"strand":1,"description":"Bardet-Biedl syndrome 1 [Source:HGNC Symbol;Acc:HGNC:966]"}, {"versioned_ensembl_gene_id":"ENSG00000256473.1","gene_symbol":"AC087260.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23637973,"end":23638487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197168.11","gene_symbol":"NEK5","gene_name":"NIMA related kinase 5 [Source:HGNC Symbol;Acc:HGNC:7748]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341676","summary":null,"start":52033611,"end":52129078,"strand":-1,"description":"NIMA related kinase 5 [Source:HGNC Symbol;Acc:HGNC:7748]"}, {"versioned_ensembl_gene_id":"ENSG00000220949.2","gene_symbol":"AC008543.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11756533,"end":11759933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283365.1","gene_symbol":"AC007603.3","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":49954985,"end":49968730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246363.2","gene_symbol":"LINC02458","gene_name":"long intergenic non-protein coding RNA 2458 [Source:HGNC Symbol;Acc:HGNC:53394]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728084","summary":null,"start":89010681,"end":89019679,"strand":-1,"description":"long intergenic non-protein coding RNA 2458 [Source:HGNC Symbol;Acc:HGNC:53394]"}, {"versioned_ensembl_gene_id":"ENSG00000101981.10","gene_symbol":"F9","gene_name":"coagulation factor IX [Source:HGNC Symbol;Acc:HGNC:3551]","synonyms":"FIX","biotype":"protein_coding","ncbi_id":"2158","summary":"This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Sep 2015]","start":139530758,"end":139563458,"strand":1,"description":"coagulation factor IX [Source:HGNC Symbol;Acc:HGNC:3551]"}, {"versioned_ensembl_gene_id":"ENSG00000105261.7","gene_symbol":"OVOL3","gene_name":"ovo like zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:14186]","synonyms":"HOVO3","biotype":"protein_coding","ncbi_id":"728361","summary":null,"start":36111151,"end":36113711,"strand":1,"description":"ovo like zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:14186]"}, {"versioned_ensembl_gene_id":"ENSG00000279774.1","gene_symbol":"AL590483.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":244064330,"end":244067909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250979.1","gene_symbol":"AC022905.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72202751,"end":72251565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279209.1","gene_symbol":"AP001002.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91013787,"end":91015299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102760.12","gene_symbol":"RGCC","gene_name":"regulator of cell cycle [Source:HGNC Symbol;Acc:HGNC:20369]","synonyms":"RGC32,RGC-32,C13orf15,bA157L14.2","biotype":"protein_coding","ncbi_id":"28984","summary":"This gene is thought to regulate cell cycle progression. It is induced by p53 in response to DNA damage, or by sublytic levels of complement system proteins that result in activation of the cell cycle. The encoded protein localizes to the cytoplasm during interphase and to centrosomes during mitosis. The protein forms a complex with polo-like kinase 1. The protein also translocates to the nucleus in response to treatment with complement system proteins, and can associate with and increase the kinase activity of cell division cycle 2 protein. In different assays and cell types, overexpression of this protein has been shown to activate or suppress cell cycle progression. [provided by RefSeq, Jul 2008]","start":41457559,"end":41470882,"strand":1,"description":"regulator of cell cycle [Source:HGNC Symbol;Acc:HGNC:20369]"}, {"versioned_ensembl_gene_id":"ENSG00000169964.7","gene_symbol":"TMEM42","gene_name":"transmembrane protein 42 [Source:HGNC Symbol;Acc:HGNC:28444]","synonyms":"MGC29956","biotype":"protein_coding","ncbi_id":"131616","summary":null,"start":44861869,"end":44865670,"strand":1,"description":"transmembrane protein 42 [Source:HGNC Symbol;Acc:HGNC:28444]"}, {"versioned_ensembl_gene_id":"ENSG00000105254.11","gene_symbol":"TBCB","gene_name":"tubulin folding cofactor B [Source:HGNC Symbol;Acc:HGNC:1989]","synonyms":"CKAPI,CKAP1,CG22","biotype":"protein_coding","ncbi_id":"1155","summary":null,"start":36114289,"end":36125947,"strand":1,"description":"tubulin folding cofactor B [Source:HGNC Symbol;Acc:HGNC:1989]"}, {"versioned_ensembl_gene_id":"ENSG00000241317.1","gene_symbol":"AL133481.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79504073,"end":79506281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000018189.12","gene_symbol":"RUFY3","gene_name":"RUN and FYVE domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30285]","synonyms":"ZFYVE30,Singar1,RIPx,KIAA0871","biotype":"protein_coding","ncbi_id":"22902","summary":"This gene encodes a RPIP8, UNC-14, and NESCA domain-containing protein that is required for maintenance of neuronal polarity. In addition, it has been implicated in mediation of gastric cancer cell migration and invasion via interaction with P21-activated kinase-1, which promotes its expression. The encoded protein localizes to F-actin-enriched invadopodia to induce formation of protrusions, thereby facilitating cell migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":70704204,"end":70807315,"strand":1,"description":"RUN and FYVE domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30285]"}, {"versioned_ensembl_gene_id":"ENSG00000282466.1","gene_symbol":"TRBV5-4","gene_name":"T-cell receptor beta variable 5-4 [Source:HGNC Symbol;Acc:HGNC:12221]","synonyms":"TCRBV5S4,TRBV54,TCRBV5S6A3N2T","biotype":"TR_V_gene","ncbi_id":"28611","summary":null,"start":142484618,"end":142485283,"strand":1,"description":"T-cell receptor beta variable 5-4 [Source:HGNC Symbol;Acc:HGNC:12221]"}, {"versioned_ensembl_gene_id":"ENSG00000150636.17","gene_symbol":"CCDC102B","gene_name":"coiled-coil domain containing 102B [Source:HGNC Symbol;Acc:HGNC:26295]","synonyms":"HsT1731,FLJ23594,C18orf14,AN,ACY1L","biotype":"protein_coding","ncbi_id":"79839","summary":null,"start":68715209,"end":69055189,"strand":1,"description":"coiled-coil domain containing 102B [Source:HGNC Symbol;Acc:HGNC:26295]"}, {"versioned_ensembl_gene_id":"ENSG00000280476.1","gene_symbol":"AC116165.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23144031,"end":23147890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254510.1","gene_symbol":"AP001107.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":66409158,"end":66417137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242061.1","gene_symbol":"AL160314.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22694098,"end":22694535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132840.9","gene_symbol":"BHMT2","gene_name":"betaine--homocysteine S-methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:1048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23743","summary":"Homocysteine is a sulfur-containing amino acid that plays a crucial role in methylation reactions. Transfer of the methyl group from betaine to homocysteine creates methionine, which donates the methyl group to methylate DNA, proteins, lipids, and other intracellular metabolites. The protein encoded by this gene is one of two methyl transferases that can catalyze the transfer of the methyl group from betaine to homocysteine. Anomalies in homocysteine metabolism have been implicated in disorders ranging from vascular disease to neural tube birth defects such as spina bifida. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":79069717,"end":79089466,"strand":1,"description":"betaine--homocysteine S-methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:1048]"}, {"versioned_ensembl_gene_id":"ENSG00000230611.1","gene_symbol":"HMGB1P27","gene_name":"high mobility group box 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100527948","summary":null,"start":191174233,"end":191174835,"strand":1,"description":"high mobility group box 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39118]"}, {"versioned_ensembl_gene_id":"ENSG00000119616.11","gene_symbol":"FCF1","gene_name":"FCF1, rRNA-processing protein [Source:HGNC Symbol;Acc:HGNC:20220]","synonyms":"Bka,UTP24,CGI-35,C14orf111","biotype":"protein_coding","ncbi_id":"51077","summary":null,"start":74713144,"end":74738620,"strand":1,"description":"FCF1, rRNA-processing protein [Source:HGNC Symbol;Acc:HGNC:20220]"}, {"versioned_ensembl_gene_id":"ENSG00000256982.1","gene_symbol":"AC135782.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89046172,"end":89052965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113391.18","gene_symbol":"FAM172A","gene_name":"family with sequence similarity 172 member A [Source:HGNC Symbol;Acc:HGNC:25365]","synonyms":"DKFZP564D172,C5orf21","biotype":"protein_coding","ncbi_id":"83989","summary":null,"start":93618069,"end":94111699,"strand":-1,"description":"family with sequence similarity 172 member A [Source:HGNC Symbol;Acc:HGNC:25365]"}, {"versioned_ensembl_gene_id":"ENSG00000277978.1","gene_symbol":"AC010542.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66565620,"end":66566001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265472.1","gene_symbol":"AC022655.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67707929,"end":67708246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229257.2","gene_symbol":"AL807752.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":137057663,"end":137062461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228960.6","gene_symbol":"OR2A9P","gene_name":"olfactory receptor family 2 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:8236]","synonyms":"OR2A9,HSDJ0798C17","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441295","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":144294480,"end":144300934,"strand":1,"description":"olfactory receptor family 2 subfamily A member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:8236]"}, {"versioned_ensembl_gene_id":"ENSG00000091583.10","gene_symbol":"APOH","gene_name":"apolipoprotein H [Source:HGNC Symbol;Acc:HGNC:616]","synonyms":"BG,B2G1","biotype":"protein_coding","ncbi_id":"350","summary":"Apolipoprotein H, also known as beta-2-glycoprotein I, is a component of circulating plasma lipoproteins. It has been implicated in a variety of physiologic pathways including lipoprotein metabolism, coagulation, hemostasis, and the production of antiphospholipid autoantibodies. APOH may be a required cofactor for anionic phospholipid binding by the antiphospholipid autoantibodies found in sera of many patients with lupus and primary antiphospholipid syndrome (APS). The anti-beta (2) glycoprotein I antibodies from APS patients, mediate inhibition of activated protein C which has anticoagulant properties. Because beta-2-GPI is the main autoantigen in patients with APS, the disruption of this pathway by autoantibodies may be an important mechanism for thrombosis in patients with APS.[provided by RefSeq, Dec 2019]","start":66212033,"end":66256525,"strand":-1,"description":"apolipoprotein H [Source:HGNC Symbol;Acc:HGNC:616]"}, {"versioned_ensembl_gene_id":"ENSG00000077454.15","gene_symbol":"LRCH4","gene_name":"leucine rich repeats and calponin homology domain containing 4 [Source:HGNC Symbol;Acc:HGNC:6691]","synonyms":"LRRN1,LRN","biotype":"protein_coding","ncbi_id":"4034","summary":"This gene encodes a protein that contains leucine-rich repeats (LRR) at its amino terminus and that is known to be involved in ligand binding. The carboxyl terminus may act as a membrane anchor. Identified structural elements suggest that the encoded protein resembles a receptor. [provided by RefSeq, Jul 2008]","start":100574011,"end":100586153,"strand":-1,"description":"leucine rich repeats and calponin homology domain containing 4 [Source:HGNC Symbol;Acc:HGNC:6691]"}, {"versioned_ensembl_gene_id":"ENSG00000261543.1","gene_symbol":"AC010931.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74152800,"end":74179226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282786.1","gene_symbol":"AF188030.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1729770,"end":1731018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007516.13","gene_symbol":"BAIAP3","gene_name":"BAI1 associated protein 3 [Source:HGNC Symbol;Acc:HGNC:948]","synonyms":"KIAA0734,BAP3","biotype":"protein_coding","ncbi_id":"8938","summary":"This p53-target gene encodes a brain-specific angiogenesis inhibitor. The protein is a seven-span transmembrane protein and a member of the secretin receptor family. It interacts with the cytoplasmic region of brain-specific angiogenesis inhibitor 1. This protein also contains two C2 domains, which are often found in proteins involved in signal transduction or membrane trafficking. Its expression pattern and similarity to other proteins suggest that it may be involved in synaptic functions. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":1333601,"end":1349441,"strand":1,"description":"BAI1 associated protein 3 [Source:HGNC Symbol;Acc:HGNC:948]"}, {"versioned_ensembl_gene_id":"ENSG00000008018.8","gene_symbol":"PSMB1","gene_name":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]","synonyms":"PMSB1,HC5","biotype":"protein_coding","ncbi_id":"5689","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is tightly linked to the TBP (TATA-binding protein) gene in human and in mouse, and is transcribed in the opposite orientation in both species. [provided by RefSeq, Jul 2008]","start":170535117,"end":170553341,"strand":-1,"description":"proteasome subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9537]"}, {"versioned_ensembl_gene_id":"ENSG00000214485.6","gene_symbol":"RPL7P1","gene_name":"ribosomal protein L7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10367]","synonyms":"RPL7P,RPL17P","biotype":"processed_pseudogene","ncbi_id":"6174","summary":null,"start":150094302,"end":150095048,"strand":1,"description":"ribosomal protein L7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10367]"}, {"versioned_ensembl_gene_id":"ENSG00000183763.8","gene_symbol":"TRAIP","gene_name":"TRAF interacting protein [Source:HGNC Symbol;Acc:HGNC:30764]","synonyms":"TRIP,RNF206","biotype":"protein_coding","ncbi_id":"10293","summary":"This gene encodes a protein that contains an N-terminal RING finger motif and a putative coiled-coil domain. A similar murine protein interacts with TNFR-associated factor 1 (TRAF1), TNFR-associated factor 2 (TRAF2), and cylindromatosis. The interaction with TRAF2 inhibits TRAF2-mediated nuclear factor kappa-B, subunit 1 activation that is required for cell activation and protection against apoptosis. [provided by RefSeq, Jul 2008]","start":49828599,"end":49856574,"strand":-1,"description":"TRAF interacting protein [Source:HGNC Symbol;Acc:HGNC:30764]"}, {"versioned_ensembl_gene_id":"ENSG00000260105.6","gene_symbol":"AOC4P","gene_name":"amine oxidase, copper containing 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:48869]","synonyms":"UPAT","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"90586","summary":null,"start":42865922,"end":42874369,"strand":1,"description":"amine oxidase, copper containing 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:48869]"}, {"versioned_ensembl_gene_id":"ENSG00000264569.1","gene_symbol":"AC137723.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82037905,"end":82039380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214553.9","gene_symbol":"LRRC37A11P","gene_name":"leucine rich repeat containing 37 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:43815]","synonyms":"LRRC37F","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"342666","summary":null,"start":39027277,"end":39053205,"strand":1,"description":"leucine rich repeat containing 37 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:43815]"}, {"versioned_ensembl_gene_id":"ENSG00000179055.7","gene_symbol":"OR13D1","gene_name":"olfactory receptor family 13 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:14695]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286365","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104694379,"end":104695485,"strand":1,"description":"olfactory receptor family 13 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:14695]"}, {"versioned_ensembl_gene_id":"ENSG00000235248.3","gene_symbol":"OR13C1P","gene_name":"olfactory receptor family 13 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14699]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"392377","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":104655363,"end":104659055,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14699]"}, {"versioned_ensembl_gene_id":"ENSG00000162572.20","gene_symbol":"SCNN1D","gene_name":"sodium channel epithelial 1 delta subunit [Source:HGNC Symbol;Acc:HGNC:10601]","synonyms":"ENaCdelta,dNaCh","biotype":"protein_coding","ncbi_id":"6339","summary":null,"start":1280436,"end":1292029,"strand":1,"description":"sodium channel epithelial 1 delta subunit [Source:HGNC Symbol;Acc:HGNC:10601]"}, {"versioned_ensembl_gene_id":"ENSG00000232183.1","gene_symbol":"AL031386.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138627077,"end":138627343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248540.2","gene_symbol":"AC010931.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74125915,"end":74129278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160877.5","gene_symbol":"NACC1","gene_name":"nucleus accumbens associated 1 [Source:HGNC Symbol;Acc:HGNC:20967]","synonyms":"BTBD30,BTBD14B,BEND8,NAC1,NAC-1","biotype":"protein_coding","ncbi_id":"112939","summary":"This gene encodes a member of the BTB/POZ protein family. BTB/POZ proteins are involved in several cellular processes including proliferation, apoptosis and transcription regulation. The encoded protein is a transcriptional repressor that plays a role in stem cell self-renewal and pluripotency maintenance. The encoded protein also suppresses transcription of the candidate tumor suppressor Gadd45GIP1, and expression of this gene may play a role in the progression of multiple types of cancer. A pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Feb 2012]","start":13118103,"end":13141141,"strand":1,"description":"nucleus accumbens associated 1 [Source:HGNC Symbol;Acc:HGNC:20967]"}, {"versioned_ensembl_gene_id":"ENSG00000233765.1","gene_symbol":"AL591479.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66253424,"end":66254464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274181.1","gene_symbol":"RBPJP2","gene_name":"RBPJ pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5726]","synonyms":"RBPSUHP2,IGKJRBP2","biotype":"processed_pseudogene","ncbi_id":"3517","summary":null,"start":66635754,"end":66637197,"strand":1,"description":"RBPJ pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5726]"}, {"versioned_ensembl_gene_id":"ENSG00000229585.4","gene_symbol":"AC110792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53986587,"end":53987058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256630.1","gene_symbol":"AC090424.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128437778,"end":128439206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279180.1","gene_symbol":"AC061709.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":128288159,"end":128289056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123453.17","gene_symbol":"SARDH","gene_name":"sarcosine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:10536]","synonyms":"SDH,DMGDHL1","biotype":"protein_coding","ncbi_id":"1757","summary":"This gene encodes an enzyme localized to the mitochondrial matrix which catalyzes the oxidative demethylation of sarcosine. This enzyme is distinct from another mitochondrial matrix enzyme, dimethylglycine dehydrogenase, which catalyzes a reaction resulting in the formation of sarcosine. Mutations in this gene are associated with sarcosinemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2008]","start":133663560,"end":133739955,"strand":-1,"description":"sarcosine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:10536]"}, {"versioned_ensembl_gene_id":"ENSG00000164398.12","gene_symbol":"ACSL6","gene_name":"acyl-CoA synthetase long chain family member 6 [Source:HGNC Symbol;Acc:HGNC:16496]","synonyms":"LACS5,LACS2,KIAA0837,FACL6,ACS2","biotype":"protein_coding","ncbi_id":"23305","summary":"The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2011]","start":131949973,"end":132012243,"strand":-1,"description":"acyl-CoA synthetase long chain family member 6 [Source:HGNC Symbol;Acc:HGNC:16496]"}, {"versioned_ensembl_gene_id":"ENSG00000234758.1","gene_symbol":"AC034228.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131944408,"end":131968220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120063.9","gene_symbol":"GNA13","gene_name":"G protein subunit alpha 13 [Source:HGNC Symbol;Acc:HGNC:4381]","synonyms":"MGC46138,G13","biotype":"protein_coding","ncbi_id":"10672","summary":null,"start":65010715,"end":65056839,"strand":-1,"description":"G protein subunit alpha 13 [Source:HGNC Symbol;Acc:HGNC:4381]"}, {"versioned_ensembl_gene_id":"ENSG00000048028.11","gene_symbol":"USP28","gene_name":"ubiquitin specific peptidase 28 [Source:HGNC Symbol;Acc:HGNC:12625]","synonyms":"KIAA1515","biotype":"protein_coding","ncbi_id":"57646","summary":"The protein encoded by this gene is a deubiquitinase involved in the DNA damage pathway and DNA damage-induced apoptosis. Overexpression of this gene is seen in several cancers. [provided by RefSeq, Oct 2016]","start":113797874,"end":113875570,"strand":-1,"description":"ubiquitin specific peptidase 28 [Source:HGNC Symbol;Acc:HGNC:12625]"}, {"versioned_ensembl_gene_id":"ENSG00000266644.1","gene_symbol":"AC103810.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64899766,"end":64900716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228063.1","gene_symbol":"LYPLAL1-AS1","gene_name":"LYPLAL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50560]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"643723","summary":null,"start":219086602,"end":219173961,"strand":-1,"description":"LYPLAL1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50560]"}, {"versioned_ensembl_gene_id":"ENSG00000167633.18","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816468,"end":54830778,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000187147.17","gene_symbol":"RNF220","gene_name":"ring finger protein 220 [Source:HGNC Symbol;Acc:HGNC:25552]","synonyms":"FLJ10597,C1orf164","biotype":"protein_coding","ncbi_id":"55182","summary":null,"start":44405194,"end":44651724,"strand":1,"description":"ring finger protein 220 [Source:HGNC Symbol;Acc:HGNC:25552]"}, {"versioned_ensembl_gene_id":"ENSG00000250166.2","gene_symbol":"AC087241.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22601425,"end":22618867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257023.1","gene_symbol":"AC087241.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22609228,"end":22625015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211888.2","gene_symbol":"TRAJ1","gene_name":"T-cell receptor alpha joining 1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12037]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28754","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22545037,"end":22545098,"strand":1,"description":"T-cell receptor alpha joining 1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12037]"}, {"versioned_ensembl_gene_id":"ENSG00000230607.3","gene_symbol":"AC005722.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19755244,"end":19756207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154719.13","gene_symbol":"MRPL39","gene_name":"mitochondrial ribosomal protein L39 [Source:HGNC Symbol;Acc:HGNC:14027]","synonyms":"RPML5,PRED66,PRED22,MSTP003,MRP-L5,MGC3400,MGC104174,L39mt,FLJ20451,C21orf92","biotype":"protein_coding","ncbi_id":"54148","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Two transcript variants encoding distinct isoforms have been described. A pseudogene corresponding to this gene is found on chromosome 5q. [provided by RefSeq, Jul 2008]","start":25585656,"end":25607517,"strand":-1,"description":"mitochondrial ribosomal protein L39 [Source:HGNC Symbol;Acc:HGNC:14027]"}, {"versioned_ensembl_gene_id":"ENSG00000237166.1","gene_symbol":"LINC01792","gene_name":"long intergenic non-protein coding RNA 1792 [Source:HGNC Symbol;Acc:HGNC:52582]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507140","summary":null,"start":200712305,"end":200735177,"strand":-1,"description":"long intergenic non-protein coding RNA 1792 [Source:HGNC Symbol;Acc:HGNC:52582]"}, {"versioned_ensembl_gene_id":"ENSG00000214702.6","gene_symbol":"AC010931.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":74097106,"end":74098414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127580.15","gene_symbol":"WDR24","gene_name":"WD repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:20852]","synonyms":"JFP7,DKFZp434F054,C16orf21","biotype":"protein_coding","ncbi_id":"84219","summary":null,"start":684622,"end":690444,"strand":-1,"description":"WD repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:20852]"}, {"versioned_ensembl_gene_id":"ENSG00000270714.1","gene_symbol":"AC132812.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64747264,"end":64747492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231503.4","gene_symbol":"PTMAP4","gene_name":"prothymosin, alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9627]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5761","summary":null,"start":9239986,"end":9240331,"strand":-1,"description":"prothymosin, alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:9627]"}, {"versioned_ensembl_gene_id":"ENSG00000258789.1","gene_symbol":"AL162171.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88551597,"end":88552493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183981.8","gene_symbol":"MAGEA13P","gene_name":"MAGE family member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:35154]","synonyms":"LOC139363","biotype":"processed_pseudogene","ncbi_id":"139363","summary":null,"start":138482745,"end":138483695,"strand":1,"description":"MAGE family member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:35154]"}, {"versioned_ensembl_gene_id":"ENSG00000103496.14","gene_symbol":"STX4","gene_name":"syntaxin 4 [Source:HGNC Symbol;Acc:HGNC:11439]","synonyms":"STX4A,p35-2","biotype":"protein_coding","ncbi_id":"6810","summary":null,"start":31032889,"end":31042975,"strand":1,"description":"syntaxin 4 [Source:HGNC Symbol;Acc:HGNC:11439]"}, {"versioned_ensembl_gene_id":"ENSG00000211877.1","gene_symbol":"TRAJ12","gene_name":"T-cell receptor alpha joining 12 [Source:HGNC Symbol;Acc:HGNC:12040]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28743","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22531939,"end":22531998,"strand":1,"description":"T-cell receptor alpha joining 12 [Source:HGNC Symbol;Acc:HGNC:12040]"}, {"versioned_ensembl_gene_id":"ENSG00000229543.1","gene_symbol":"AC010163.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78293842,"end":78301003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255468.6","gene_symbol":"AP001107.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66347950,"end":66364804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108958.4","gene_symbol":"AC130689.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1858039,"end":1858446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141127.14","gene_symbol":"PRPSAP2","gene_name":"phosphoribosyl pyrophosphate synthetase associated protein 2 [Source:HGNC Symbol;Acc:HGNC:9467]","synonyms":"PAP41","biotype":"protein_coding","ncbi_id":"5636","summary":"This gene encodes a protein that associates with the enzyme phosphoribosylpyrophosphate synthetase (PRS). PRS catalyzes the formation of phosphoribosylpyrophosphate which is a substrate for synthesis of purine and pyrimidine nucleotides, histidine, tryptophan and NAD. PRS exists as a complex with two catalytic subunits and two associated subunits. This gene encodes a non-catalytic associated subunit of PRS. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":18840085,"end":18931287,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase associated protein 2 [Source:HGNC Symbol;Acc:HGNC:9467]"}, {"versioned_ensembl_gene_id":"ENSG00000211868.1","gene_symbol":"TRAJ21","gene_name":"T-cell receptor alpha joining 21 [Source:HGNC Symbol;Acc:HGNC:12050]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28734","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22523600,"end":22523654,"strand":1,"description":"T-cell receptor alpha joining 21 [Source:HGNC Symbol;Acc:HGNC:12050]"}, {"versioned_ensembl_gene_id":"ENSG00000236123.1","gene_symbol":"CEACAMP11","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:1823]","synonyms":"CGM18","biotype":"unprocessed_pseudogene","ncbi_id":"1086","summary":null,"start":43278933,"end":43284318,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:1823]"}, {"versioned_ensembl_gene_id":"ENSG00000112246.9","gene_symbol":"SIM1","gene_name":"single-minded family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10882]","synonyms":"bHLHe14","biotype":"protein_coding","ncbi_id":"6492","summary":"SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or cognitive disability of Down syndrome. [provided by RefSeq, Jul 2008]","start":100385015,"end":100464929,"strand":-1,"description":"single-minded family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10882]"}, {"versioned_ensembl_gene_id":"ENSG00000276985.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54945648,"end":54961872,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000228082.1","gene_symbol":"Z86062.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100427118,"end":100437484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166333.13","gene_symbol":"ILK","gene_name":"integrin linked kinase [Source:HGNC Symbol;Acc:HGNC:6040]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3611","summary":"This gene encodes a protein with a kinase-like domain and four ankyrin-like repeats. The encoded protein associates at the cell membrane with the cytoplasmic domain of beta integrins, where it regulates integrin-mediated signal transduction. Activity of this protein is important in the epithelial to mesenchymal transition, and over-expression of this gene is implicated in tumor growth and metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":6603708,"end":6610874,"strand":1,"description":"integrin linked kinase [Source:HGNC Symbol;Acc:HGNC:6040]"}, {"versioned_ensembl_gene_id":"ENSG00000248200.2","gene_symbol":"AC093770.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110146374,"end":110147248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211865.1","gene_symbol":"TRAJ24","gene_name":"T-cell receptor alpha joining 24 [Source:HGNC Symbol;Acc:HGNC:12053]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28731","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22519969,"end":22520031,"strand":1,"description":"T-cell receptor alpha joining 24 [Source:HGNC Symbol;Acc:HGNC:12053]"}, {"versioned_ensembl_gene_id":"ENSG00000211863.1","gene_symbol":"TRAJ26","gene_name":"T-cell receptor alpha joining 26 [Source:HGNC Symbol;Acc:HGNC:12055]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28729","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22518446,"end":22518505,"strand":1,"description":"T-cell receptor alpha joining 26 [Source:HGNC Symbol;Acc:HGNC:12055]"}, {"versioned_ensembl_gene_id":"ENSG00000277003.1","gene_symbol":"AC026468.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69975238,"end":69975344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216378.1","gene_symbol":"AL080285.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100177209,"end":100178192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000094804.9","gene_symbol":"CDC6","gene_name":"cell division cycle 6 [Source:HGNC Symbol;Acc:HGNC:1744]","synonyms":"CDC18L","biotype":"protein_coding","ncbi_id":"990","summary":"The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc6, a protein essential for the initiation of DNA replication. This protein functions as a regulator at the early steps of DNA replication. It localizes in cell nucleus during cell cyle G1, but translocates to the cytoplasm at the start of S phase. The subcellular translocation of this protein during cell cyle is regulated through its phosphorylation by Cdks. Transcription of this protein was reported to be regulated in response to mitogenic signals through transcriptional control mechanism involving E2F proteins. [provided by RefSeq, Jul 2008]","start":40287633,"end":40304657,"strand":1,"description":"cell division cycle 6 [Source:HGNC Symbol;Acc:HGNC:1744]"}, {"versioned_ensembl_gene_id":"ENSG00000256022.5","gene_symbol":"LINC02411","gene_name":"long intergenic non-protein coding RNA 2411 [Source:HGNC Symbol;Acc:HGNC:53340]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927637","summary":null,"start":127631248,"end":127636467,"strand":-1,"description":"long intergenic non-protein coding RNA 2411 [Source:HGNC Symbol;Acc:HGNC:53340]"}, {"versioned_ensembl_gene_id":"ENSG00000119888.10","gene_symbol":"EPCAM","gene_name":"epithelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:11529]","synonyms":"CD326,HEA125,MOC31,323/A3,GA733-2,MK-1,17-1A,ESA,MIC18,Ep-CAM,MH99,EGP40,M4S1,EGP34,Ly74,TROP1,EGP-2,KSA,TACSTD1,CO-17A,KS1/4,TACST-1","biotype":"protein_coding","ncbi_id":"4072","summary":"This gene encodes a carcinoma-associated antigen and is a member of a family that includes at least two type I membrane proteins. This antigen is expressed on most normal epithelial cells and gastrointestinal carcinomas and functions as a homotypic calcium-independent cell adhesion molecule. The antigen is being used as a target for immunotherapy treatment of human carcinomas. Mutations in this gene result in congenital tufting enteropathy. [provided by RefSeq, Dec 2008]","start":47345158,"end":47387601,"strand":1,"description":"epithelial cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:11529]"}, {"versioned_ensembl_gene_id":"ENSG00000259227.2","gene_symbol":"AC087699.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70602124,"end":70602516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237584.1","gene_symbol":"RAC1P4","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31113]","synonyms":"RAC4,Psi4Rac1","biotype":"processed_pseudogene","ncbi_id":"286472","summary":null,"start":137441258,"end":137441836,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31113]"}, {"versioned_ensembl_gene_id":"ENSG00000249183.1","gene_symbol":"SUMO2P4","gene_name":"SUMO2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39014]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288757","summary":null,"start":69068925,"end":69069200,"strand":-1,"description":"SUMO2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39014]"}, {"versioned_ensembl_gene_id":"ENSG00000162444.11","gene_symbol":"RBP7","gene_name":"retinol binding protein 7 [Source:HGNC Symbol;Acc:HGNC:30316]","synonyms":"CRBPIV","biotype":"protein_coding","ncbi_id":"116362","summary":"The protein encoded by this gene is a member of the cellular retinol-binding protein (CRBP) family, whose members are required for vitamin A stability and metabolism. The encoded protein binds all-trans-retinol and is structurally similar to other CRBPs; however, it has a lower binding affinity for retinol than other CRBPs. [provided by RefSeq, Aug 2016]","start":9997206,"end":10016020,"strand":1,"description":"retinol binding protein 7 [Source:HGNC Symbol;Acc:HGNC:30316]"}, {"versioned_ensembl_gene_id":"ENSG00000187581.2","gene_symbol":"COX8C","gene_name":"cytochrome c oxidase subunit 8C [Source:HGNC Symbol;Acc:HGNC:24382]","synonyms":"COX8-3","biotype":"protein_coding","ncbi_id":"341947","summary":null,"start":93347191,"end":93348356,"strand":1,"description":"cytochrome c oxidase subunit 8C [Source:HGNC Symbol;Acc:HGNC:24382]"}, {"versioned_ensembl_gene_id":"ENSG00000213730.3","gene_symbol":"POLD2P1","gene_name":"DNA polymerase delta 2, accessory subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41522]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391811","summary":null,"start":93267429,"end":93268425,"strand":1,"description":"DNA polymerase delta 2, accessory subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41522]"}, {"versioned_ensembl_gene_id":"ENSG00000258976.1","gene_symbol":"AC013451.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74614693,"end":74616647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254645.1","gene_symbol":"AC087379.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15701963,"end":15758898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260032.1","gene_symbol":"NORAD","gene_name":"non-coding RNA activated by DNA damage [Source:HGNC Symbol;Acc:HGNC:44311]","synonyms":"LINC00657","biotype":"lincRNA","ncbi_id":"647979","summary":null,"start":36045622,"end":36050960,"strand":-1,"description":"non-coding RNA activated by DNA damage [Source:HGNC Symbol;Acc:HGNC:44311]"}, {"versioned_ensembl_gene_id":"ENSG00000248588.1","gene_symbol":"AC008517.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92826255,"end":92844004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229016.1","gene_symbol":"AC096638.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":218301262,"end":218301972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112238.11","gene_symbol":"PRDM13","gene_name":"PR/SET domain 13 [Source:HGNC Symbol;Acc:HGNC:13998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59336","summary":null,"start":99606730,"end":99615578,"strand":1,"description":"PR/SET domain 13 [Source:HGNC Symbol;Acc:HGNC:13998]"}, {"versioned_ensembl_gene_id":"ENSG00000214253.8","gene_symbol":"FIS1","gene_name":"fission, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:21689]","synonyms":"TTC11,H_NH0132A01.6,Fis1,CGI-135","biotype":"protein_coding","ncbi_id":"51024","summary":"The balance between fission and fusion regulates the morphology of mitochondria. TTC11 is a component of a mitochondrial complex that promotes mitochondrial fission (James et al., 2003 [PubMed 12783892]).[supplied by OMIM, Mar 2008]","start":101239458,"end":101252316,"strand":-1,"description":"fission, mitochondrial 1 [Source:HGNC Symbol;Acc:HGNC:21689]"}, {"versioned_ensembl_gene_id":"ENSG00000249984.1","gene_symbol":"AC026780.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92675956,"end":92688254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163710.7","gene_symbol":"PCOLCE2","gene_name":"procollagen C-endopeptidase enhancer 2 [Source:HGNC Symbol;Acc:HGNC:8739]","synonyms":"PCPE2","biotype":"protein_coding","ncbi_id":"26577","summary":null,"start":142815922,"end":142889203,"strand":-1,"description":"procollagen C-endopeptidase enhancer 2 [Source:HGNC Symbol;Acc:HGNC:8739]"}, {"versioned_ensembl_gene_id":"ENSG00000219806.1","gene_symbol":"ATP5F1P6","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39747]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645440","summary":null,"start":139614438,"end":139615204,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39747]"}, {"versioned_ensembl_gene_id":"ENSG00000275318.1","gene_symbol":"AL136981.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92840955,"end":92841688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235040.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32706124,"end":32706955,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000165169.10","gene_symbol":"DYNLT3","gene_name":"dynein light chain Tctex-type 3 [Source:HGNC Symbol;Acc:HGNC:11694]","synonyms":"TCTEX1L,TCTE1L","biotype":"protein_coding","ncbi_id":"6990","summary":"This gene encodes a member of a subclass of dynein light chains. The encoded protein homodimerizes and forms the light chain component of the cytoplasmic dynein motor protein complex. This protein may be important for binding dynein to specific cargos including the spindle checkpoint protein BUB3. This protein may also function independently of dynein as a transcriptional modulator. Pseudogenes of this gene are found on chromosomes 2 and 20.[provided by RefSeq, Mar 2010]","start":37836757,"end":37847637,"strand":-1,"description":"dynein light chain Tctex-type 3 [Source:HGNC Symbol;Acc:HGNC:11694]"}, {"versioned_ensembl_gene_id":"ENSG00000282148.1","gene_symbol":"TRBV5-3","gene_name":"T-cell receptor beta variable 5-3 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12220]","synonyms":"TRBV53,TCRBV5S5P,TCRBV5S3","biotype":"TR_V_gene","ncbi_id":"28612","summary":null,"start":142410913,"end":142411379,"strand":1,"description":"T-cell receptor beta variable 5-3 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12220]"}, {"versioned_ensembl_gene_id":"ENSG00000282318.1","gene_symbol":"DLGAP2","gene_name":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]","synonyms":"ERICH1-AS1,ERICH1-AS1,DAP2,DAP-2,C8orf68,SAPAP2,C8orf68","biotype":"protein_coding","ncbi_id":"9228","summary":"The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]","start":1627028,"end":1708042,"strand":1,"description":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]"}, {"versioned_ensembl_gene_id":"ENSG00000279879.1","gene_symbol":"AC091152.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44689858,"end":44693340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258426.1","gene_symbol":"AL162872.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83018201,"end":83039602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230853.1","gene_symbol":"RPL10P11","gene_name":"ribosomal protein L10 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128030","summary":null,"start":80096600,"end":80097215,"strand":-1,"description":"ribosomal protein L10 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36565]"}, {"versioned_ensembl_gene_id":"ENSG00000258743.5","gene_symbol":"LINC02301","gene_name":"long intergenic non-protein coding RNA 2301 [Source:HGNC Symbol;Acc:HGNC:53220]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928599","summary":null,"start":82642620,"end":82706825,"strand":1,"description":"long intergenic non-protein coding RNA 2301 [Source:HGNC Symbol;Acc:HGNC:53220]"}, {"versioned_ensembl_gene_id":"ENSG00000234110.1","gene_symbol":"TSPY25P","gene_name":"testis specific protein, Y-linked 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:38726]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874288","summary":null,"start":9624183,"end":9626352,"strand":1,"description":"testis specific protein, Y-linked 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:38726]"}, {"versioned_ensembl_gene_id":"ENSG00000130254.11","gene_symbol":"SAFB2","gene_name":"scaffold attachment factor B2 [Source:HGNC Symbol;Acc:HGNC:21605]","synonyms":"KIAA0138","biotype":"protein_coding","ncbi_id":"9667","summary":"The protein encoded by this gene, along with its paralog (scaffold attachment factor B1), is a repressor of estrogen receptor alpha. The encoded protein binds scaffold/matrix attachment region (S/MAR) DNA and is involved in cell cycle regulation, apoptosis, differentiation, the stress response, and regulation of immune genes. [provided by RefSeq, May 2016]","start":5586999,"end":5624046,"strand":-1,"description":"scaffold attachment factor B2 [Source:HGNC Symbol;Acc:HGNC:21605]"}, {"versioned_ensembl_gene_id":"ENSG00000274465.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54860636,"end":54875223,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000138356.13","gene_symbol":"AOX1","gene_name":"aldehyde oxidase 1 [Source:HGNC Symbol;Acc:HGNC:553]","synonyms":"AOH1,AO","biotype":"protein_coding","ncbi_id":"316","summary":"Aldehyde oxidase produces hydrogen peroxide and, under certain conditions, can catalyze the formation of superoxide. Aldehyde oxidase is a candidate gene for amyotrophic lateral sclerosis. [provided by RefSeq, Jul 2008]","start":200585868,"end":200677064,"strand":1,"description":"aldehyde oxidase 1 [Source:HGNC Symbol;Acc:HGNC:553]"}, {"versioned_ensembl_gene_id":"ENSG00000162896.5","gene_symbol":"PIGR","gene_name":"polymeric immunoglobulin receptor [Source:HGNC Symbol;Acc:HGNC:8968]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5284","summary":"This gene is a member of the immunoglobulin superfamily. The encoded poly-Ig receptor binds polymeric immunoglobulin molecules at the basolateral surface of epithelial cells; the complex is then transported across the cell to be secreted at the apical surface. A significant association was found between immunoglobulin A nephropathy and several SNPs in this gene.[provided by RefSeq, Sep 2009]","start":206928518,"end":206946466,"strand":-1,"description":"polymeric immunoglobulin receptor [Source:HGNC Symbol;Acc:HGNC:8968]"}, {"versioned_ensembl_gene_id":"ENSG00000215029.8","gene_symbol":"TCP11X2","gene_name":"t-complex 11 family, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:48335]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100996648","summary":null,"start":102374628,"end":102471812,"strand":-1,"description":"t-complex 11 family, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:48335]"}, {"versioned_ensembl_gene_id":"ENSG00000226890.1","gene_symbol":"Z97652.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1625628,"end":1626160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237232.7","gene_symbol":"ZNF295-AS1","gene_name":"ZNF295 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23130]","synonyms":"PRED87,NCRNA00318,C21orf121","biotype":"lincRNA","ncbi_id":"150142","summary":null,"start":42009194,"end":42024924,"strand":1,"description":"ZNF295 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23130]"}, {"versioned_ensembl_gene_id":"ENSG00000260347.1","gene_symbol":"MOCS1P1","gene_name":"molybdenum cofactor synthesis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7191]","synonyms":"MOCS1P2","biotype":"processed_pseudogene","ncbi_id":"27187","summary":null,"start":48496990,"end":48498601,"strand":1,"description":"molybdenum cofactor synthesis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7191]"}, {"versioned_ensembl_gene_id":"ENSG00000224393.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"C6orf25,G6b-B,G6b,NG31","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31700763,"end":31708879,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000259533.1","gene_symbol":"AC040958.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63885851,"end":63886051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260021.1","gene_symbol":"AC098934.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":202810238,"end":202810829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186174.12","gene_symbol":"BCL9L","gene_name":"B-cell CLL/lymphoma 9 like [Source:HGNC Symbol;Acc:HGNC:23688]","synonyms":"DLNB11","biotype":"protein_coding","ncbi_id":"283149","summary":null,"start":118893875,"end":118925608,"strand":-1,"description":"B-cell CLL/lymphoma 9 like [Source:HGNC Symbol;Acc:HGNC:23688]"}, {"versioned_ensembl_gene_id":"ENSG00000132155.11","gene_symbol":"RAF1","gene_name":"Raf-1 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:9829]","synonyms":"c-Raf,Raf-1,CRAF","biotype":"protein_coding","ncbi_id":"5894","summary":"This gene is the cellular homolog of viral raf gene (v-raf). The encoded protein is a MAP kinase kinase kinase (MAP3K), which functions downstream of the Ras family of membrane associated GTPases to which it binds directly. Once activated, the cellular RAF1 protein can phosphorylate to activate the dual specificity protein kinases MEK1 and MEK2, which in turn phosphorylate to activate the serine/threonine specific protein kinases, ERK1 and ERK2. Activated ERKs are pleiotropic effectors of cell physiology and play an important role in the control of gene expression involved in the cell division cycle, apoptosis, cell differentiation and cell migration. Mutations in this gene are associated with Noonan syndrome 5 and LEOPARD syndrome 2. [provided by RefSeq, Jul 2008]","start":12583601,"end":12664226,"strand":-1,"description":"Raf-1 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:9829]"}, {"versioned_ensembl_gene_id":"ENSG00000100220.11","gene_symbol":"RTCB","gene_name":"RNA 2',3'-cyclic phosphate and 5'-OH ligase [Source:HGNC Symbol;Acc:HGNC:26935]","synonyms":"HSPC117,FAAP,C22orf28","biotype":"protein_coding","ncbi_id":"51493","summary":null,"start":32387582,"end":32412255,"strand":-1,"description":"RNA 2',3'-cyclic phosphate and 5'-OH ligase [Source:HGNC Symbol;Acc:HGNC:26935]"}, {"versioned_ensembl_gene_id":"ENSG00000175701.10","gene_symbol":"LINC00116","gene_name":"long intergenic non-protein coding RNA 116 [Source:HGNC Symbol;Acc:HGNC:27339]","synonyms":"NCRNA00116","biotype":"protein_coding","ncbi_id":"205251","summary":null,"start":110211529,"end":110245420,"strand":-1,"description":"long intergenic non-protein coding RNA 116 [Source:HGNC Symbol;Acc:HGNC:27339]"}, {"versioned_ensembl_gene_id":"ENSG00000248456.1","gene_symbol":"LINC02485","gene_name":"long intergenic non-protein coding RNA 2485 [Source:HGNC Symbol;Acc:HGNC:53460]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377439","summary":null,"start":135112905,"end":135123779,"strand":-1,"description":"long intergenic non-protein coding RNA 2485 [Source:HGNC Symbol;Acc:HGNC:53460]"}, {"versioned_ensembl_gene_id":"ENSG00000230865.1","gene_symbol":"TSEN15P1","gene_name":"tRNA splicing endonuclease subunit 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43962]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288179","summary":null,"start":17456427,"end":17457259,"strand":1,"description":"tRNA splicing endonuclease subunit 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43962]"}, {"versioned_ensembl_gene_id":"ENSG00000225945.1","gene_symbol":"AL121574.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37815777,"end":37819218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211821.2","gene_symbol":"TRDV2","gene_name":"T-cell receptor delta variable 2 [Source:HGNC Symbol;Acc:HGNC:12263]","synonyms":"MGC117421,hDV102S1","biotype":"TR_V_gene","ncbi_id":"28517","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22422371,"end":22423042,"strand":1,"description":"T-cell receptor delta variable 2 [Source:HGNC Symbol;Acc:HGNC:12263]"}, {"versioned_ensembl_gene_id":"ENSG00000165660.7","gene_symbol":"ABRAXAS2","gene_name":"abraxas 2, BRISC complex subunit [Source:HGNC Symbol;Acc:HGNC:28975]","synonyms":"KIAA0157,FAM175B,Em:AC068896.4,ABRO1","biotype":"protein_coding","ncbi_id":"23172","summary":null,"start":124801785,"end":124836670,"strand":1,"description":"abraxas 2, BRISC complex subunit [Source:HGNC Symbol;Acc:HGNC:28975]"}, {"versioned_ensembl_gene_id":"ENSG00000213218.10","gene_symbol":"CSH2","gene_name":"chorionic somatomammotropin hormone 2 [Source:HGNC Symbol;Acc:HGNC:2441]","synonyms":"hCS-B,CSB,CS-2","biotype":"protein_coding","ncbi_id":"1443","summary":"The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms of each of the five growth hormones. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, while the ratio of 1 to 2 increases by term. Structural and expression differences provide avenues for developmental regulation and tissue specificity. [provided by RefSeq, Jul 2008]","start":63872012,"end":63873766,"strand":-1,"description":"chorionic somatomammotropin hormone 2 [Source:HGNC Symbol;Acc:HGNC:2441]"}, {"versioned_ensembl_gene_id":"ENSG00000213786.3","gene_symbol":"NHP2P2","gene_name":"NHP2 ribonucleoprotein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22797]","synonyms":"TCAG_30283","biotype":"processed_pseudogene","ncbi_id":"442290","summary":null,"start":27048169,"end":27048628,"strand":1,"description":"NHP2 ribonucleoprotein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22797]"}, {"versioned_ensembl_gene_id":"ENSG00000205309.13","gene_symbol":"NT5M","gene_name":"5',3'-nucleotidase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:15769]","synonyms":"mdN,dNT2,dNT-2","biotype":"protein_coding","ncbi_id":"56953","summary":"This gene encodes a 5' nucleotidase that localizes to the mitochondrial matrix. This enzyme dephosphorylates the 5'- and 2'(3')-phosphates of uracil and thymine deoxyribonucleotides. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":17303335,"end":17347663,"strand":1,"description":"5',3'-nucleotidase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:15769]"}, {"versioned_ensembl_gene_id":"ENSG00000249779.1","gene_symbol":"AC106800.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43206709,"end":43207811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226196.1","gene_symbol":"GAPDHP75","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:50648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652918","summary":null,"start":189132350,"end":189133292,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:50648]"}, {"versioned_ensembl_gene_id":"ENSG00000262919.7","gene_symbol":"FAM58A","gene_name":"family with sequence similarity 58 member A [Source:HGNC Symbol;Acc:HGNC:28434]","synonyms":"CCNQ","biotype":"protein_coding","ncbi_id":"92002","summary":"Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":153587919,"end":153600045,"strand":-1,"description":"family with sequence similarity 58 member A [Source:HGNC Symbol;Acc:HGNC:28434]"}, {"versioned_ensembl_gene_id":"ENSG00000260081.1","gene_symbol":"AF274858.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153599340,"end":153604353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128039.10","gene_symbol":"SRD5A3","gene_name":"steroid 5 alpha-reductase 3 [Source:HGNC Symbol;Acc:HGNC:25812]","synonyms":"FLJ13352,SRD5A2L1,SRD5A2L","biotype":"protein_coding","ncbi_id":"79644","summary":"The protein encoded by this gene belongs to the steroid 5-alpha reductase family, and polyprenol reductase subfamily. It is involved in the production of androgen 5-alpha-dihydrotestosterone (DHT) from testosterone, and maintenance of the androgen-androgen receptor activation pathway. This protein is also necessary for the conversion of polyprenol into dolichol, which is required for the synthesis of dolichol-linked monosaccharides and the oligosaccharide precursor used for N-linked glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type Iq. [provided by RefSeq, Mar 2011]","start":55346109,"end":55373096,"strand":1,"description":"steroid 5 alpha-reductase 3 [Source:HGNC Symbol;Acc:HGNC:25812]"}, {"versioned_ensembl_gene_id":"ENSG00000224208.1","gene_symbol":"AL590762.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71314912,"end":71315879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241891.1","gene_symbol":"RPL9P6","gene_name":"ribosomal protein L9 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19798]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326311","summary":null,"start":81777016,"end":81777613,"strand":-1,"description":"ribosomal protein L9 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19798]"}, {"versioned_ensembl_gene_id":"ENSG00000110066.14","gene_symbol":"KMT5B","gene_name":"lysine methyltransferase 5B [Source:HGNC Symbol;Acc:HGNC:24283]","synonyms":"SUV420H1,CGI-85","biotype":"protein_coding","ncbi_id":"51111","summary":"This gene encodes a protein that contains a SET domain. SET domains appear to be protein-protein interaction domains that mediate interactions with a family of proteins that display similarity with dual-specificity phosphatases (dsPTPases). The function of this gene has not been determined. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":68154863,"end":68213828,"strand":-1,"description":"lysine methyltransferase 5B [Source:HGNC Symbol;Acc:HGNC:24283]"}, {"versioned_ensembl_gene_id":"ENSG00000250425.1","gene_symbol":"AC098976.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9754898,"end":9755778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259281.1","gene_symbol":"LINGO1-AS2","gene_name":"LINGO1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51423]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929478","summary":null,"start":77660052,"end":77668074,"strand":1,"description":"LINGO1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51423]"}, {"versioned_ensembl_gene_id":"ENSG00000259666.2","gene_symbol":"LINGO1-AS1","gene_name":"LINGO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27368]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"253044","summary":null,"start":77641764,"end":77652288,"strand":1,"description":"LINGO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27368]"}, {"versioned_ensembl_gene_id":"ENSG00000108604.15","gene_symbol":"SMARCD2","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 [Source:HGNC Symbol;Acc:HGNC:11107]","synonyms":"Rsc6p,PRO2451,CRACD2,BAF60B","biotype":"protein_coding","ncbi_id":"6603","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63832081,"end":63843065,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 [Source:HGNC Symbol;Acc:HGNC:11107]"}, {"versioned_ensembl_gene_id":"ENSG00000251035.1","gene_symbol":"WBP1LP4","gene_name":"WW domain binding protein 1-like pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43951]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480779","summary":null,"start":181378695,"end":181379038,"strand":-1,"description":"WW domain binding protein 1-like pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43951]"}, {"versioned_ensembl_gene_id":"ENSG00000269937.1","gene_symbol":"AC093525.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2561471,"end":2565096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230472.5","gene_symbol":"AL135908.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50587607,"end":50637205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224069.1","gene_symbol":"BX842559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154897561,"end":154898092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234668.3","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G2,NG38,ATP6G,Em:AC004181.3,Vma10","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31526639,"end":31529021,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000131844.15","gene_symbol":"MCCC2","gene_name":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]","synonyms":"MCCB","biotype":"protein_coding","ncbi_id":"64087","summary":"This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018]","start":71587288,"end":71658704,"strand":1,"description":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]"}, {"versioned_ensembl_gene_id":"ENSG00000127533.3","gene_symbol":"F2RL3","gene_name":"F2R like thrombin or trypsin receptor 3 [Source:HGNC Symbol;Acc:HGNC:3540]","synonyms":"PAR4","biotype":"protein_coding","ncbi_id":"9002","summary":"This gene encodes a member of the protease-activated receptor subfamily, part of the G-protein coupled receptor 1 family of proteins. The encoded receptor is proteolytically processed to reveal an extracellular N-terminal tethered ligand that binds to and activates the receptor. This receptor plays a role in blood coagulation, inflammation and response to pain. Hypomethylation at this gene may be associated with lung cancer in human patients. [provided by RefSeq, Sep 2016]","start":16888860,"end":16892606,"strand":1,"description":"F2R like thrombin or trypsin receptor 3 [Source:HGNC Symbol;Acc:HGNC:3540]"}, {"versioned_ensembl_gene_id":"ENSG00000240063.1","gene_symbol":"AC069431.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":182783236,"end":182793394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229750.1","gene_symbol":"AC096649.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":175167904,"end":175168522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106070.17","gene_symbol":"GRB10","gene_name":"growth factor receptor bound protein 10 [Source:HGNC Symbol;Acc:HGNC:4564]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2887","summary":"The product of this gene belongs to a small family of adapter proteins that are known to interact with a number of receptor tyrosine kinases and signaling molecules. This gene encodes a growth factor receptor-binding protein that interacts with insulin receptors and insulin-like growth-factor receptors. Overexpression of some isoforms of the encoded protein inhibits tyrosine kinase activity and results in growth suppression. This gene is imprinted in a highly isoform- and tissue-specific manner, with expression observed from the paternal allele in the brain, and from the maternal allele in the placental trophoblasts. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2010]","start":50590063,"end":50793462,"strand":-1,"description":"growth factor receptor bound protein 10 [Source:HGNC Symbol;Acc:HGNC:4564]"}, {"versioned_ensembl_gene_id":"ENSG00000070770.8","gene_symbol":"CSNK2A2","gene_name":"casein kinase 2 alpha 2 [Source:HGNC Symbol;Acc:HGNC:2459]","synonyms":"CSNK2A1,CK2alpha'","biotype":"protein_coding","ncbi_id":"1459","summary":"This gene encodes the alpha', or alpha 2, catalytic subunit of the protein kinase enzyme, casein kinase 2 (CK2). Casein kinase 2 is a serine/threonine protein kinase that phosphorylates acidic proteins such as casein. It is involved in various cellular processes, including cell cycle control, apoptosis, and circadian rhythms. This heterotetrameric kinase includes two catalytic subunits, either alpha or alpha', and two regulatory beta subunits. The closely related gene paralog encoding the alpha, or alpha 1 subunit (CSNK2A1, Gene ID: 1457) is found on chromosome 20. An intronic variant in this gene (alpha 2) may be associated with leukocyte telomere length in a South Asian population. A related transcribed pseudogene is found on chromosome 11. [provided by RefSeq, Aug 2017]","start":58157907,"end":58197920,"strand":-1,"description":"casein kinase 2 alpha 2 [Source:HGNC Symbol;Acc:HGNC:2459]"}, {"versioned_ensembl_gene_id":"ENSG00000213131.3","gene_symbol":"YWHAZP4","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30851]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246737","summary":null,"start":127355756,"end":127356789,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30851]"}, {"versioned_ensembl_gene_id":"ENSG00000232823.2","gene_symbol":"TXNP1","gene_name":"thioredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49481]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"93202","summary":null,"start":119683127,"end":119683823,"strand":-1,"description":"thioredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49481]"}, {"versioned_ensembl_gene_id":"ENSG00000248373.5","gene_symbol":"AC096577.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104907357,"end":105120000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250942.1","gene_symbol":"ENPP7P11","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48694]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421806","summary":null,"start":9677308,"end":9677934,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48694]"}, {"versioned_ensembl_gene_id":"ENSG00000228092.1","gene_symbol":"COX6CP15","gene_name":"cytochrome c oxidase subunit 6C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480268","summary":null,"start":77433572,"end":77433782,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49368]"}, {"versioned_ensembl_gene_id":"ENSG00000261603.1","gene_symbol":"PRSS46","gene_name":"protease, serine 46 [Source:HGNC Symbol;Acc:HGNC:37325]","synonyms":"TESSP6","biotype":"protein_coding","ncbi_id":"100287362","summary":null,"start":46719583,"end":46736429,"strand":-1,"description":"protease, serine 46 [Source:HGNC Symbol;Acc:HGNC:37325]"}, {"versioned_ensembl_gene_id":"ENSG00000099204.18","gene_symbol":"ABLIM1","gene_name":"actin binding LIM protein 1 [Source:HGNC Symbol;Acc:HGNC:78]","synonyms":"limatin,LIMAB1,ABLIM","biotype":"protein_coding","ncbi_id":"3983","summary":"This gene encodes a LIM zinc-binding domain-containing protein that binds to actin filaments and mediates interactions between actin and cytoplasmic targets. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2017]","start":114431113,"end":114685003,"strand":-1,"description":"actin binding LIM protein 1 [Source:HGNC Symbol;Acc:HGNC:78]"}, {"versioned_ensembl_gene_id":"ENSG00000226074.4","gene_symbol":"PRSS44","gene_name":"protease, serine 44 [Source:HGNC Symbol;Acc:HGNC:37324]","synonyms":"TESSP4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729756","summary":null,"start":46809359,"end":46812558,"strand":-1,"description":"protease, serine 44 [Source:HGNC Symbol;Acc:HGNC:37324]"}, {"versioned_ensembl_gene_id":"ENSG00000284672.1","gene_symbol":"AC109583.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46742092,"end":46812558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232611.1","gene_symbol":"AL683813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136840931,"end":136847797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251388.1","gene_symbol":"AC079380.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133871246,"end":134010690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120784.15","gene_symbol":"ZFP30","gene_name":"ZFP30 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:29555]","synonyms":"ZNF745,KIAA0961","biotype":"protein_coding","ncbi_id":"22835","summary":null,"start":37613749,"end":37692337,"strand":-1,"description":"ZFP30 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:29555]"}, {"versioned_ensembl_gene_id":"ENSG00000174408.8","gene_symbol":"PPIAP24","gene_name":"peptidylprolyl isomerase A pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39269]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122335","summary":null,"start":106863816,"end":106864286,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39269]"}, {"versioned_ensembl_gene_id":"ENSG00000228377.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486298,"end":29487434,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000124302.12","gene_symbol":"CHST8","gene_name":"carbohydrate sulfotransferase 8 [Source:HGNC Symbol;Acc:HGNC:15993]","synonyms":"GALNAC-4-ST1","biotype":"protein_coding","ncbi_id":"64377","summary":"The protein encoded by this gene belongs to the sulfotransferase 2 family. It is predominantly expressed in the pituitary gland, and is localized to the golgi membrane. This protein catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. It is responsible for sulfation of GalNAc on luteinizing hormone (LH), which is required for production of the sex hormones. Mice lacking this enzyme, exhibit increased levels of circulating LH, and precocious sexual maturation of both male and female mice. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":33621955,"end":33773509,"strand":1,"description":"carbohydrate sulfotransferase 8 [Source:HGNC Symbol;Acc:HGNC:15993]"}, {"versioned_ensembl_gene_id":"ENSG00000282643.1","gene_symbol":"DLGAP2-AS1","gene_name":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507435","summary":null,"start":1565035,"end":1621861,"strand":-1,"description":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]"}, {"versioned_ensembl_gene_id":"ENSG00000263155.5","gene_symbol":"MYZAP","gene_name":"myocardial zonula adherens protein [Source:HGNC Symbol;Acc:HGNC:43444]","synonyms":"MYOZAP,Gup1,Gup,GCOM1","biotype":"protein_coding","ncbi_id":"100820829","summary":"This gene encodes a protein that is abundantly expressed in cardiac tissue. The encoded protein localizes to intercalated discs in cardiomyocytes and functions as an activator of Rho-dependent serum-response factor signaling. Alternative splicing results in multiple transcript variants. Readthrough transcription also exists between this gene and the neighboring downstream gene POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) and is represented with GeneID: 145781. [provided by RefSeq, Mar 2014]","start":57591941,"end":57685364,"strand":1,"description":"myocardial zonula adherens protein [Source:HGNC Symbol;Acc:HGNC:43444]"}, {"versioned_ensembl_gene_id":"ENSG00000272625.1","gene_symbol":"AP000919.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2920966,"end":2921685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148842.17","gene_symbol":"CNNM2","gene_name":"cyclin and CBS domain divalent metal cation transport mediator 2 [Source:HGNC Symbol;Acc:HGNC:103]","synonyms":"ACDP2","biotype":"protein_coding","ncbi_id":"54805","summary":"This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play an important role in magnesium homeostasis by mediating the epithelial transport and renal reabsorption of Mg2+. Mutations in this gene are associated with renal hypomagnesemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":102918293,"end":103090221,"strand":1,"description":"cyclin and CBS domain divalent metal cation transport mediator 2 [Source:HGNC Symbol;Acc:HGNC:103]"}, {"versioned_ensembl_gene_id":"ENSG00000238046.1","gene_symbol":"MTND5P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42284]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873260","summary":null,"start":124680722,"end":124680916,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42284]"}, {"versioned_ensembl_gene_id":"ENSG00000270607.1","gene_symbol":"AC009549.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19710934,"end":19712619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170950.5","gene_symbol":"PGK2","gene_name":"phosphoglycerate kinase 2 [Source:HGNC Symbol;Acc:HGNC:8898]","synonyms":"PGKPS,PGK-2","biotype":"protein_coding","ncbi_id":"5232","summary":"This gene is intronless, arose via retrotransposition of the phosphoglycerate kinase 1 gene, and is expressed specifically in the testis. Initially assumed to be a pseudogene, the encoded protein is actually a functional phosphoglycerate kinase that catalyzes the reversible conversion of 1,3-bisphosphoglycerate to 3-phosphoglycerate, during the Embden-Meyerhof-Parnas pathway of glycolysis, in the later stages of spermatogenesis.[provided by RefSeq, May 2010]","start":49785651,"end":49787307,"strand":-1,"description":"phosphoglycerate kinase 2 [Source:HGNC Symbol;Acc:HGNC:8898]"}, {"versioned_ensembl_gene_id":"ENSG00000230045.4","gene_symbol":"FAM90A15P","gene_name":"family with sequence similarity 90 member A15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32263]","synonyms":"FAM90A15","biotype":"unprocessed_pseudogene","ncbi_id":"389630","summary":"FAM90A15 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7256904,"end":7259914,"strand":1,"description":"family with sequence similarity 90 member A15, pseudogene [Source:HGNC Symbol;Acc:HGNC:32263]"}, {"versioned_ensembl_gene_id":"ENSG00000215012.8","gene_symbol":"RTL10","gene_name":"retrotransposon Gag like 10 [Source:HGNC Symbol;Acc:HGNC:26112]","synonyms":"FLJ21125,C22orf29,BOP","biotype":"protein_coding","ncbi_id":"79680","summary":null,"start":19846138,"end":19854896,"strand":-1,"description":"retrotransposon Gag like 10 [Source:HGNC Symbol;Acc:HGNC:26112]"}, {"versioned_ensembl_gene_id":"ENSG00000204406.12","gene_symbol":"MBD5","gene_name":"methyl-CpG binding domain protein 5 [Source:HGNC Symbol;Acc:HGNC:20444]","synonyms":"KIAA1461,FLJ11113","biotype":"protein_coding","ncbi_id":"55777","summary":"This gene encodes a member of the methyl-CpG-binding domain (MBD) family. The MBD consists of about 70 residues and is the minimal region required for a methyl-CpG-binding protein binding specifically to methylated DNA. In addition to the MBD domain, this protein contains a PWWP domain (Pro-Trp-Trp-Pro motif), which consists of 100-150 amino acids and is found in numerous proteins that are involved in cell division, growth and differentiation. Mutations in this gene cause an autosomal dominant type of cognitive disability. The encoded protein interacts with the polycomb repressive complex PR-DUB which catalyzes the deubiquitination of a lysine residue of histone 2A. Haploinsufficiency of this gene is associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures. Alternatively spliced transcript variants have been found, but their full-length nature is not determined. [provided by RefSeq, Jul 2017]","start":148021011,"end":148516971,"strand":1,"description":"methyl-CpG binding domain protein 5 [Source:HGNC Symbol;Acc:HGNC:20444]"}, {"versioned_ensembl_gene_id":"ENSG00000249811.2","gene_symbol":"USP17L21","gene_name":"ubiquitin specific peptidase 17-like family member 21 [Source:HGNC Symbol;Acc:HGNC:44449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287478","summary":null,"start":9262872,"end":9264823,"strand":1,"description":"ubiquitin specific peptidase 17-like family member 21 [Source:HGNC Symbol;Acc:HGNC:44449]"}, {"versioned_ensembl_gene_id":"ENSG00000037280.15","gene_symbol":"FLT4","gene_name":"fms related tyrosine kinase 4 [Source:HGNC Symbol;Acc:HGNC:3767]","synonyms":"VEGFR3,PCL","biotype":"protein_coding","ncbi_id":"2324","summary":"This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq, Jul 2008]","start":180601506,"end":180649624,"strand":-1,"description":"fms related tyrosine kinase 4 [Source:HGNC Symbol;Acc:HGNC:3767]"}, {"versioned_ensembl_gene_id":"ENSG00000259008.1","gene_symbol":"AL355834.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57355446,"end":57359410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227075.1","gene_symbol":"AP000472.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21933315,"end":21975681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225357.3","gene_symbol":"RPF2P1","gene_name":"ribosome production factor 2 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16186]","synonyms":"RPF2P,C20orf53,BXDC1P,bA353C18.4","biotype":"processed_pseudogene","ncbi_id":"729608","summary":null,"start":35752814,"end":35753719,"strand":1,"description":"ribosome production factor 2 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16186]"}, {"versioned_ensembl_gene_id":"ENSG00000254894.1","gene_symbol":"NAV2-AS1","gene_name":"NAV2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40744]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874015","summary":null,"start":20119684,"end":20120632,"strand":-1,"description":"NAV2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40744]"}, {"versioned_ensembl_gene_id":"ENSG00000233989.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464526,"end":29469736,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000250804.1","gene_symbol":"AC073648.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8981436,"end":8982360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227178.2","gene_symbol":"BX908738.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29290710,"end":29291652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270073.1","gene_symbol":"TSPY6P","gene_name":"testis specific protein, Y-linked 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:34039]","synonyms":"TSPYP6","biotype":"unprocessed_pseudogene","ncbi_id":"653174","summary":null,"start":9507596,"end":9510175,"strand":1,"description":"testis specific protein, Y-linked 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:34039]"}, {"versioned_ensembl_gene_id":"ENSG00000272822.1","gene_symbol":"AC073610.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":48903503,"end":48957365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233875.1","gene_symbol":"AL592078.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154579065,"end":154579663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126217.20","gene_symbol":"MCF2L","gene_name":"MCF.2 cell line derived transforming sequence like [Source:HGNC Symbol;Acc:HGNC:14576]","synonyms":"OST,KIAA0362,DBS,ARHGEF14","biotype":"protein_coding","ncbi_id":"23263","summary":"This gene encodes a guanine nucleotide exchange factor that interacts specifically with the GTP-bound Rac1 and plays a role in the Rho/Rac signaling pathways. A variant in this gene was associated with osteoarthritis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":112894378,"end":113099739,"strand":1,"description":"MCF.2 cell line derived transforming sequence like [Source:HGNC Symbol;Acc:HGNC:14576]"}, {"versioned_ensembl_gene_id":"ENSG00000236166.1","gene_symbol":"AL021408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132085084,"end":132099279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258459.1","gene_symbol":"AL356019.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20305730,"end":20306811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270212.1","gene_symbol":"AC008738.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33283978,"end":33285739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229067.1","gene_symbol":"AL714022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91600171,"end":91600321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228846.2","gene_symbol":"BX927132.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137841,"end":29138777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233636.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29111857,"end":29112792,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000225765.1","gene_symbol":"LINC01831","gene_name":"long intergenic non-protein coding RNA 1831 [Source:HGNC Symbol;Acc:HGNC:52637]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927331","summary":null,"start":104412227,"end":104414008,"strand":-1,"description":"long intergenic non-protein coding RNA 1831 [Source:HGNC Symbol;Acc:HGNC:52637]"}, {"versioned_ensembl_gene_id":"ENSG00000248122.1","gene_symbol":"APOOP4","gene_name":"apolipoprotein O pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128725","summary":null,"start":68304343,"end":68304939,"strand":-1,"description":"apolipoprotein O pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48742]"}, {"versioned_ensembl_gene_id":"ENSG00000242338.6","gene_symbol":"BMS1P4","gene_name":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23652]","synonyms":"BMS1LP4,BMS1LP4,OTTHUMG00000018478","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729096","summary":null,"start":73715843,"end":73730469,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23652]"}, {"versioned_ensembl_gene_id":"ENSG00000100568.10","gene_symbol":"VTI1B","gene_name":"vesicle transport through interaction with t-SNAREs 1B [Source:HGNC Symbol;Acc:HGNC:17793]","synonyms":"VTI2","biotype":"protein_coding","ncbi_id":"10490","summary":null,"start":67647075,"end":67674831,"strand":-1,"description":"vesicle transport through interaction with t-SNAREs 1B [Source:HGNC Symbol;Acc:HGNC:17793]"}, {"versioned_ensembl_gene_id":"ENSG00000189023.10","gene_symbol":"MAGEB16","gene_name":"MAGE family member B16 [Source:HGNC Symbol;Acc:HGNC:21188]","synonyms":null,"biotype":"protein_coding","ncbi_id":"139604","summary":null,"start":35798342,"end":35803735,"strand":1,"description":"MAGE family member B16 [Source:HGNC Symbol;Acc:HGNC:21188]"}, {"versioned_ensembl_gene_id":"ENSG00000258737.2","gene_symbol":"SUB1P2","gene_name":"SUB1 homolog, transcriptional regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43992]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287680","summary":null,"start":74305425,"end":74306527,"strand":1,"description":"SUB1 homolog, transcriptional regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43992]"}, {"versioned_ensembl_gene_id":"ENSG00000258493.2","gene_symbol":"AL121603.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34920865,"end":34921006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249197.1","gene_symbol":"OR10J9P","gene_name":"olfactory receptor family 10 subfamily J member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:19639]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391120","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":159405423,"end":159406409,"strand":-1,"description":"olfactory receptor family 10 subfamily J member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:19639]"}, {"versioned_ensembl_gene_id":"ENSG00000261853.1","gene_symbol":"AC134349.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11190733,"end":11191642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146166.16","gene_symbol":"LGSN","gene_name":"lengsin, lens protein with glutamine synthetase domain [Source:HGNC Symbol;Acc:HGNC:21016]","synonyms":"LGS,GLULD1","biotype":"protein_coding","ncbi_id":"51557","summary":"This gene encodes a protein with similarity to the GS I members of the glutamine synthetase superfamily. The encoded protein is referred to as a pseudo-glutamine synthetase because it has no glutamine synthesis activity and may function as a chaperone protein. This protein is localized to the lens and may be associated with cataract disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":63275951,"end":63319977,"strand":-1,"description":"lengsin, lens protein with glutamine synthetase domain [Source:HGNC Symbol;Acc:HGNC:21016]"}, {"versioned_ensembl_gene_id":"ENSG00000270719.1","gene_symbol":"AL390877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117700029,"end":117700242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153140.8","gene_symbol":"CETN3","gene_name":"centrin 3 [Source:HGNC Symbol;Acc:HGNC:1868]","synonyms":"CEN3","biotype":"protein_coding","ncbi_id":"1070","summary":"The protein encoded by this gene contains four EF-hand calcium binding domains, and is a member of the centrin protein family. Centrins are evolutionarily conserved proteins similar to the CDC31 protein of S. cerevisiae. Yeast CDC31 is located at the centrosome of interphase and mitotic cells, where it plays a fundamental role in centrosome duplication and separation. Multiple forms of the proteins similar to the yeast centrin have been identified in human and other mammalian cells, some of which have been shown to be associated with centrosome fractions. This protein appears to be one of the most abundant centrins associated with centrosome, which suggests a similar function to its yeast counterpart. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":90392261,"end":90409786,"strand":-1,"description":"centrin 3 [Source:HGNC Symbol;Acc:HGNC:1868]"}, {"versioned_ensembl_gene_id":"ENSG00000068971.13","gene_symbol":"PPP2R5B","gene_name":"protein phosphatase 2 regulatory subunit B'beta [Source:HGNC Symbol;Acc:HGNC:9310]","synonyms":"PR61B,FLJ35411,B56beta,B56B","biotype":"protein_coding","ncbi_id":"5526","summary":"The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a beta isoform of the regulatory subunit B56 subfamily. [provided by RefSeq, Jul 2008]","start":64917553,"end":64934473,"strand":1,"description":"protein phosphatase 2 regulatory subunit B'beta [Source:HGNC Symbol;Acc:HGNC:9310]"}, {"versioned_ensembl_gene_id":"ENSG00000273604.1","gene_symbol":"EPOP","gene_name":"elongin BC and polycomb repressive complex 2 associated protein [Source:HGNC Symbol;Acc:HGNC:34493]","synonyms":"PRR28,LOC100170841,C17orf96","biotype":"protein_coding","ncbi_id":"100170841","summary":null,"start":38671703,"end":38675421,"strand":-1,"description":"elongin BC and polycomb repressive complex 2 associated protein [Source:HGNC Symbol;Acc:HGNC:34493]"}, {"versioned_ensembl_gene_id":"ENSG00000137403.19","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29716754,"end":29732497,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000251581.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29735695,"end":29742934,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000156920.10","gene_symbol":"ADGRG4","gene_name":"adhesion G protein-coupled receptor G4 [Source:HGNC Symbol;Acc:HGNC:18992]","synonyms":"RP1-299I16,PGR17,GPR112","biotype":"protein_coding","ncbi_id":"139378","summary":"This gene encodes a G-protein coupled receptor belonging to a large family of diverse integral membrane proteins that participate in various physiological functions. Members of this superfamily are characterized by a signature 7-transmembrane domain motif. The ligand for this family member is unknown, and it is therefore an orphan receptor. This receptor is known to be expressed in normal enterochromaffin cells and in gastrointestinal neuroendocrine carcinoma cells, and it is therefore considered to be a novel biomarker or target for immunotherapy. [provided by RefSeq, May 2010]","start":136300963,"end":136416888,"strand":1,"description":"adhesion G protein-coupled receptor G4 [Source:HGNC Symbol;Acc:HGNC:18992]"}, {"versioned_ensembl_gene_id":"ENSG00000251253.1","gene_symbol":"MTHFD2P4","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131135","summary":null,"start":162322188,"end":162323907,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48862]"}, {"versioned_ensembl_gene_id":"ENSG00000272712.1","gene_symbol":"TAS2R8","gene_name":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]","synonyms":"TRB5,T2R8","biotype":"protein_coding","ncbi_id":"50836","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10806051,"end":10807293,"strand":-1,"description":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]"}, {"versioned_ensembl_gene_id":"ENSG00000234120.1","gene_symbol":"AF228730.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7112314,"end":7113728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106991.13","gene_symbol":"ENG","gene_name":"endoglin [Source:HGNC Symbol;Acc:HGNC:3349]","synonyms":"ORW1,ORW,HHT1,END,CD105","biotype":"protein_coding","ncbi_id":"2022","summary":"This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]","start":127815012,"end":127854756,"strand":-1,"description":"endoglin [Source:HGNC Symbol;Acc:HGNC:3349]"}, {"versioned_ensembl_gene_id":"ENSG00000128573.24","gene_symbol":"FOXP2","gene_name":"forkhead box P2 [Source:HGNC Symbol;Acc:HGNC:13875]","synonyms":"TNRC10,SPCH1,CAGH44","biotype":"protein_coding","ncbi_id":"93986","summary":"This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]","start":114086327,"end":114693772,"strand":1,"description":"forkhead box P2 [Source:HGNC Symbol;Acc:HGNC:13875]"}, {"versioned_ensembl_gene_id":"ENSG00000215251.3","gene_symbol":"FASTKD5","gene_name":"FAST kinase domains 5 [Source:HGNC Symbol;Acc:HGNC:25790]","synonyms":"FLJ13149","biotype":"protein_coding","ncbi_id":"60493","summary":null,"start":3146519,"end":3159897,"strand":-1,"description":"FAST kinase domains 5 [Source:HGNC Symbol;Acc:HGNC:25790]"}, {"versioned_ensembl_gene_id":"ENSG00000173193.13","gene_symbol":"PARP14","gene_name":"poly(ADP-ribose) polymerase family member 14 [Source:HGNC Symbol;Acc:HGNC:29232]","synonyms":"pART8,KIAA1268","biotype":"protein_coding","ncbi_id":"54625","summary":"This gene encodes a member of the poly(ADP-ribose) polymerase (PARP) protein family. The encoded anti-apoptotic protein may regulate aerobic glycolysis and promote survival of cancer cells. Increased expression of this gene has been reported in a variety of tumor types. [provided by RefSeq, Jul 2016]","start":122680618,"end":122730840,"strand":1,"description":"poly(ADP-ribose) polymerase family member 14 [Source:HGNC Symbol;Acc:HGNC:29232]"}, {"versioned_ensembl_gene_id":"ENSG00000260646.1","gene_symbol":"AL031705.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1512979,"end":1514675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282842.1","gene_symbol":"FRG2EP","gene_name":"FSHD region gene 2 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:51365]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"647476","summary":null,"start":29415264,"end":29416911,"strand":-1,"description":"FSHD region gene 2 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:51365]"}, {"versioned_ensembl_gene_id":"ENSG00000278923.2","gene_symbol":"AP005242.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15056845,"end":15066598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128564.6","gene_symbol":"VGF","gene_name":"VGF nerve growth factor inducible [Source:HGNC Symbol;Acc:HGNC:12684]","synonyms":"SgVII,SCG7","biotype":"protein_coding","ncbi_id":"7425","summary":"This gene is specifically expressed in a subpopulation of neuroendocrine cells, and is upregulated by nerve growth factor. The structural organization of this gene is similar to that of the rat gene, and both the translated and the untranslated regions show a high degree of sequence similarity to the rat gene. The encoded secretory protein also shares similarities with the secretogranin/chromogranin family, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":101162509,"end":101165593,"strand":-1,"description":"VGF nerve growth factor inducible [Source:HGNC Symbol;Acc:HGNC:12684]"}, {"versioned_ensembl_gene_id":"ENSG00000282279.1","gene_symbol":"AC243658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46046922,"end":46047379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233168.1","gene_symbol":"CR753509.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29262722,"end":29264098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165813.18","gene_symbol":"CCDC186","gene_name":"coiled-coil domain containing 186 [Source:HGNC Symbol;Acc:HGNC:24349]","synonyms":"FLJ35301,FLJ10188,C10orf118","biotype":"protein_coding","ncbi_id":"55088","summary":null,"start":114120862,"end":114174220,"strand":-1,"description":"coiled-coil domain containing 186 [Source:HGNC Symbol;Acc:HGNC:24349]"}, {"versioned_ensembl_gene_id":"ENSG00000175768.12","gene_symbol":"TOMM5","gene_name":"translocase of outer mitochondrial membrane 5 [Source:HGNC Symbol;Acc:HGNC:31369]","synonyms":"Tom5,C9orf105,bA613M10.3","biotype":"protein_coding","ncbi_id":"401505","summary":null,"start":37582646,"end":37592642,"strand":-1,"description":"translocase of outer mitochondrial membrane 5 [Source:HGNC Symbol;Acc:HGNC:31369]"}, {"versioned_ensembl_gene_id":"ENSG00000125631.7","gene_symbol":"HTR5BP","gene_name":"5-hydroxytryptamine receptor 5B, pseudogene [Source:HGNC Symbol;Acc:HGNC:16291]","synonyms":"HTR5B,GPR134,5-HT5B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645694","summary":null,"start":117859427,"end":117934942,"strand":1,"description":"5-hydroxytryptamine receptor 5B, pseudogene [Source:HGNC Symbol;Acc:HGNC:16291]"}, {"versioned_ensembl_gene_id":"ENSG00000255306.1","gene_symbol":"AC004923.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68024809,"end":68030461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271158.1","gene_symbol":"AL450472.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135464329,"end":135465484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124201.14","gene_symbol":"ZNFX1","gene_name":"zinc finger NFX1-type containing 1 [Source:HGNC Symbol;Acc:HGNC:29271]","synonyms":"FLJ11277,KIAA1404","biotype":"protein_coding","ncbi_id":"57169","summary":null,"start":49237946,"end":49278426,"strand":-1,"description":"zinc finger NFX1-type containing 1 [Source:HGNC Symbol;Acc:HGNC:29271]"}, {"versioned_ensembl_gene_id":"ENSG00000111540.15","gene_symbol":"RAB5B","gene_name":"RAB5B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9784]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5869","summary":null,"start":55973913,"end":55996683,"strand":1,"description":"RAB5B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9784]"}, {"versioned_ensembl_gene_id":"ENSG00000205030.1","gene_symbol":"OR5L2","gene_name":"olfactory receptor family 5 subfamily L member 2 [Source:HGNC Symbol;Acc:HGNC:8351]","synonyms":"HTPCRX16,HSHTPCRX16","biotype":"protein_coding","ncbi_id":"26338","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55827219,"end":55828154,"strand":1,"description":"olfactory receptor family 5 subfamily L member 2 [Source:HGNC Symbol;Acc:HGNC:8351]"}, {"versioned_ensembl_gene_id":"ENSG00000232852.1","gene_symbol":"CICP4","gene_name":"capicua transcriptional repressor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37753]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132920","summary":null,"start":64290187,"end":64292998,"strand":-1,"description":"capicua transcriptional repressor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37753]"}, {"versioned_ensembl_gene_id":"ENSG00000250250.1","gene_symbol":"CTD-2350J17.1","gene_name":"uncharacterized LOC101929472 [Source:NCBI gene;Acc:101929472]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929472","summary":null,"start":15602189,"end":15607348,"strand":-1,"description":"uncharacterized LOC101929472 [Source:NCBI gene;Acc:101929472]"}, {"versioned_ensembl_gene_id":"ENSG00000279395.3","gene_symbol":"OR5L1","gene_name":"olfactory receptor family 5 subfamily L member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8350]","synonyms":"OST262","biotype":"polymorphic_pseudogene","ncbi_id":"219437","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":55811367,"end":55812476,"strand":1,"description":"olfactory receptor family 5 subfamily L member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8350]"}, {"versioned_ensembl_gene_id":"ENSG00000173950.15","gene_symbol":"XXYLT1","gene_name":"xyloside xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26639]","synonyms":"FLJ35155,C3orf21","biotype":"protein_coding","ncbi_id":"152002","summary":null,"start":195068279,"end":195271167,"strand":-1,"description":"xyloside xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26639]"}, {"versioned_ensembl_gene_id":"ENSG00000232039.2","gene_symbol":"DEFT1P2","gene_name":"defensin, theta 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33599]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287083","summary":null,"start":7006293,"end":7007389,"strand":-1,"description":"defensin, theta 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33599]"}, {"versioned_ensembl_gene_id":"ENSG00000219163.2","gene_symbol":"HMGB1P20","gene_name":"high mobility group box 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39103]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128227","summary":null,"start":53235621,"end":53236297,"strand":-1,"description":"high mobility group box 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39103]"}, {"versioned_ensembl_gene_id":"ENSG00000232582.1","gene_symbol":"AC234771.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135135149,"end":135135770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185155.11","gene_symbol":"MIXL1","gene_name":"Mix paired-like homeobox [Source:HGNC Symbol;Acc:HGNC:13363]","synonyms":"MIXL,MILD1","biotype":"protein_coding","ncbi_id":"83881","summary":"Homeodomain proteins, such as MIXL1, are transcription factors that regulate cell fate during development (Hart et al., 2005 [PubMed 15982639]).[supplied by OMIM, Mar 2008]","start":226223618,"end":226227054,"strand":1,"description":"Mix paired-like homeobox [Source:HGNC Symbol;Acc:HGNC:13363]"}, {"versioned_ensembl_gene_id":"ENSG00000266554.1","gene_symbol":"LINC01443","gene_name":"long intergenic non-protein coding RNA 1443 [Source:HGNC Symbol;Acc:HGNC:50768]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400644","summary":null,"start":14946267,"end":14973770,"strand":1,"description":"long intergenic non-protein coding RNA 1443 [Source:HGNC Symbol;Acc:HGNC:50768]"}, {"versioned_ensembl_gene_id":"ENSG00000151729.10","gene_symbol":"SLC25A4","gene_name":"solute carrier family 25 member 4 [Source:HGNC Symbol;Acc:HGNC:10990]","synonyms":"ANT1,T1,PEO3,PEO2","biotype":"protein_coding","ncbi_id":"291","summary":"This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]","start":185143241,"end":185150382,"strand":1,"description":"solute carrier family 25 member 4 [Source:HGNC Symbol;Acc:HGNC:10990]"}, {"versioned_ensembl_gene_id":"ENSG00000220030.1","gene_symbol":"AL356131.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61240898,"end":61241311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265786.1","gene_symbol":"LINC01906","gene_name":"long intergenic non-protein coding RNA 1906 [Source:HGNC Symbol;Acc:HGNC:52725]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372011","summary":null,"start":14877611,"end":14884052,"strand":1,"description":"long intergenic non-protein coding RNA 1906 [Source:HGNC Symbol;Acc:HGNC:52725]"}, {"versioned_ensembl_gene_id":"ENSG00000276290.1","gene_symbol":"RBBP4P3","gene_name":"RB binding protein 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730180","summary":null,"start":60873360,"end":60874642,"strand":-1,"description":"RB binding protein 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42370]"}, {"versioned_ensembl_gene_id":"ENSG00000267387.1","gene_symbol":"AC020931.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10089032,"end":10090377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266774.1","gene_symbol":"AC116003.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75432703,"end":75436957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261000.1","gene_symbol":"AC244034.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206503948,"end":206504456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213684.4","gene_symbol":"LDHBP2","gene_name":"lactate dehydrogenase B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6543]","synonyms":"LDHBP,LDHBL2","biotype":"processed_pseudogene","ncbi_id":"3947","summary":null,"start":76334841,"end":76335845,"strand":-1,"description":"lactate dehydrogenase B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6543]"}, {"versioned_ensembl_gene_id":"ENSG00000274398.1","gene_symbol":"AC233981.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76250183,"end":76251796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268595.1","gene_symbol":"AC063977.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51251231,"end":51271179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206430.8","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31579125,"end":31583213,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000260710.1","gene_symbol":"AC120498.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1294551,"end":1299166,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249173.5","gene_symbol":"LINC01093","gene_name":"long intergenic non-protein coding RNA 1093 [Source:HGNC Symbol;Acc:HGNC:49218]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506229","summary":null,"start":184893871,"end":184899454,"strand":-1,"description":"long intergenic non-protein coding RNA 1093 [Source:HGNC Symbol;Acc:HGNC:49218]"}, {"versioned_ensembl_gene_id":"ENSG00000278137.1","gene_symbol":"CU151838.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268619,"end":54269662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251230.5","gene_symbol":"MIR3945HG","gene_name":"MIR3945 host gene [Source:HGNC Symbol;Acc:HGNC:52002]","synonyms":null,"biotype":"lincRNA","ncbi_id":"731424","summary":null,"start":184844585,"end":184855751,"strand":-1,"description":"MIR3945 host gene [Source:HGNC Symbol;Acc:HGNC:52002]"}, {"versioned_ensembl_gene_id":"ENSG00000164304.15","gene_symbol":"CAGE1","gene_name":"cancer antigen 1 [Source:HGNC Symbol;Acc:HGNC:21622]","synonyms":"CTAG3,CT95,bA69L16.7","biotype":"protein_coding","ncbi_id":"285782","summary":null,"start":7326656,"end":7389743,"strand":-1,"description":"cancer antigen 1 [Source:HGNC Symbol;Acc:HGNC:21622]"}, {"versioned_ensembl_gene_id":"ENSG00000175536.6","gene_symbol":"LIPT2","gene_name":"lipoyl(octanoyl) transferase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:37216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387787","summary":"This gene encodes a mitochondrial protein that catalyzes the transfer of octanoic acid to lipoate-dependent enzymes such as octanoyl-ACP. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":74491712,"end":74493733,"strand":-1,"description":"lipoyl(octanoyl) transferase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:37216]"}, {"versioned_ensembl_gene_id":"ENSG00000258931.1","gene_symbol":"AC100836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26050538,"end":26052276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258965.2","gene_symbol":"AC044913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25928146,"end":25928575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259011.1","gene_symbol":"AC016266.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25865295,"end":25877211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250316.1","gene_symbol":"AC068880.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19237737,"end":19241912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237608.1","gene_symbol":"CR388407.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071832,"end":29072607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161681.15","gene_symbol":"SHANK1","gene_name":"SH3 and multiple ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:15474]","synonyms":"synamon,SSTRIP,SPANK-1","biotype":"protein_coding","ncbi_id":"50944","summary":"This gene encodes a member of the SHANK (SH3 domain and ankyrin repeat containing) family of proteins. Members of this family act as scaffold proteins that are required for the development and function of neuronal synapses. Deletions in this gene may be associated with autism spectrum disorder in males. [provided by RefSeq, Apr 2016]","start":50661827,"end":50719450,"strand":-1,"description":"SH3 and multiple ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:15474]"}, {"versioned_ensembl_gene_id":"ENSG00000129170.8","gene_symbol":"CSRP3","gene_name":"cysteine and glycine rich protein 3 [Source:HGNC Symbol;Acc:HGNC:2472]","synonyms":"MLP,CMD1M,CLP","biotype":"protein_coding","ncbi_id":"8048","summary":"This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]","start":19182030,"end":19210573,"strand":-1,"description":"cysteine and glycine rich protein 3 [Source:HGNC Symbol;Acc:HGNC:2472]"}, {"versioned_ensembl_gene_id":"ENSG00000253539.1","gene_symbol":"AC018442.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99796615,"end":99799187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259632.2","gene_symbol":"AC090971.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51859185,"end":51861293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259712.1","gene_symbol":"AC023906.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52056675,"end":52100523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169252.5","gene_symbol":"ADRB2","gene_name":"adrenoceptor beta 2 [Source:HGNC Symbol;Acc:HGNC:286]","synonyms":"BAR,B2AR,ADRBR,ADRB2R","biotype":"protein_coding","ncbi_id":"154","summary":"This gene encodes beta-2-adrenergic receptor which is a member of the G protein-coupled receptor superfamily. This receptor is directly associated with one of its ultimate effectors, the class C L-type calcium channel Ca(V)1.2. This receptor-channel complex also contains a G protein, an adenylyl cyclase, cAMP-dependent kinase, and the counterbalancing phosphatase, PP2A. The assembly of the signaling complex provides a mechanism that ensures specific and rapid signaling by this G protein-coupled receptor. This receptor is also a transcription regulator of the alpha-synuclein gene, and together, both genes are believed to be associated with risk of Parkinson's Disease. This gene is intronless. Different polymorphic forms, point mutations, and/or downregulation of this gene are associated with nocturnal asthma, obesity, type 2 diabetes and cardiovascular disease. [provided by RefSeq, Oct 2019]","start":148825245,"end":148828687,"strand":1,"description":"adrenoceptor beta 2 [Source:HGNC Symbol;Acc:HGNC:286]"}, {"versioned_ensembl_gene_id":"ENSG00000141699.10","gene_symbol":"RETREG3","gene_name":"reticulophagy regulator family member 3 [Source:HGNC Symbol;Acc:HGNC:27258]","synonyms":"FLJ33806,FAM134C,DKFZp686B1036","biotype":"protein_coding","ncbi_id":"162427","summary":null,"start":42579513,"end":42610623,"strand":-1,"description":"reticulophagy regulator family member 3 [Source:HGNC Symbol;Acc:HGNC:27258]"}, {"versioned_ensembl_gene_id":"ENSG00000248711.1","gene_symbol":"THUMPD3P1","gene_name":"THUMP domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50793]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419989","summary":null,"start":40151613,"end":40154151,"strand":1,"description":"THUMP domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50793]"}, {"versioned_ensembl_gene_id":"ENSG00000229906.1","gene_symbol":"SNRPGP11","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39330]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874426","summary":null,"start":51496020,"end":51496251,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39330]"}, {"versioned_ensembl_gene_id":"ENSG00000237331.1","gene_symbol":"XIAP-AS1","gene_name":"XIAP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40078]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480735","summary":null,"start":123872626,"end":123873932,"strand":-1,"description":"XIAP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40078]"}, {"versioned_ensembl_gene_id":"ENSG00000101966.12","gene_symbol":"XIAP","gene_name":"X-linked inhibitor of apoptosis [Source:HGNC Symbol;Acc:HGNC:592]","synonyms":"hILP,BIRC4,API3","biotype":"protein_coding","ncbi_id":"331","summary":"This gene encodes a protein that belongs to a family of apoptotic suppressor proteins. Members of this family share a conserved motif termed, baculovirus IAP repeat, which is necessary for their anti-apoptotic function. This protein functions through binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2 and inhibits apoptosis induced by menadione, a potent inducer of free radicals, and interleukin 1-beta converting enzyme. This protein also inhibits at least two members of the caspase family of cell-death proteases, caspase-3 and caspase-7. Mutations in this gene are the cause of X-linked lymphoproliferative syndrome. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 2 and 11.[provided by RefSeq, Feb 2011]","start":123859724,"end":123913979,"strand":1,"description":"X-linked inhibitor of apoptosis [Source:HGNC Symbol;Acc:HGNC:592]"}, {"versioned_ensembl_gene_id":"ENSG00000140955.10","gene_symbol":"ADAD2","gene_name":"adenosine deaminase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30714]","synonyms":"TENRL,FLJ00337","biotype":"protein_coding","ncbi_id":"161931","summary":null,"start":84191138,"end":84197168,"strand":1,"description":"adenosine deaminase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30714]"}, {"versioned_ensembl_gene_id":"ENSG00000272316.1","gene_symbol":"AL021368.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57908560,"end":57913911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271162.1","gene_symbol":"AL022099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48952070,"end":48952781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235405.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28986213,"end":28987494,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000223809.1","gene_symbol":"AC234771.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135123239,"end":135123604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196972.8","gene_symbol":"SMIM10L2B","gene_name":"small integral membrane protein 10 like 2B [Source:HGNC Symbol;Acc:HGNC:34500]","synonyms":"RP11-85L21.2,NCRNA00087,LINC00087","biotype":"protein_coding","ncbi_id":"644596","summary":null,"start":135094987,"end":135098634,"strand":-1,"description":"small integral membrane protein 10 like 2B [Source:HGNC Symbol;Acc:HGNC:34500]"}, {"versioned_ensembl_gene_id":"ENSG00000272752.6","gene_symbol":"STAG3L5P-PVRIG2P-PILRB","gene_name":"STAG3L5P-PVRIG2P-PILRB readthrough [Source:HGNC Symbol;Acc:HGNC:48898]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101752399","summary":"This locus represents naturally occurring readthrough transcription among the neighboring LOC101735302 (stromal antigen 3 pseudogene), LOC101752334 (poliovirus receptor related immunoglobulin domain containing pseudogene) and PILRB (paired immunoglobin-like type 2 receptor beta) genes on chromosome 7. The readthrough transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Jun 2013]","start":100336104,"end":100367831,"strand":1,"description":"STAG3L5P-PVRIG2P-PILRB readthrough [Source:HGNC Symbol;Acc:HGNC:48898]"}, {"versioned_ensembl_gene_id":"ENSG00000283095.1","gene_symbol":"FP565171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131891640,"end":131895297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251059.5","gene_symbol":"AC139722.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81164940,"end":81193395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226633.2","gene_symbol":"PPIAP28","gene_name":"peptidylprolyl isomerase A pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39902]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390378","summary":null,"start":20178978,"end":20179462,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39902]"}, {"versioned_ensembl_gene_id":"ENSG00000265118.5","gene_symbol":"AC134669.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31305213,"end":31318831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224158.1","gene_symbol":"CR753651.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861425,"end":28862056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248507.1","gene_symbol":"OR5H4P","gene_name":"olfactory receptor family 5 subfamily H member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14763]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79299","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98222044,"end":98222966,"strand":1,"description":"olfactory receptor family 5 subfamily H member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14763]"}, {"versioned_ensembl_gene_id":"ENSG00000283405.1","gene_symbol":"AL121759.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21089696,"end":21090509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168298.6","gene_symbol":"HIST1H1E","gene_name":"histone cluster 1 H1 family member e [Source:HGNC Symbol;Acc:HGNC:4718]","synonyms":"H1F4,H1e,H1.4,H1s-4","biotype":"protein_coding","ncbi_id":"3008","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26156354,"end":26157107,"strand":1,"description":"histone cluster 1 H1 family member e [Source:HGNC Symbol;Acc:HGNC:4718]"}, {"versioned_ensembl_gene_id":"ENSG00000259488.2","gene_symbol":"AC023355.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48312353,"end":48331856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279480.1","gene_symbol":"AC138466.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132200436,"end":132201287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256943.1","gene_symbol":"AC148477.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132275391,"end":132278329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005981.12","gene_symbol":"ASB4","gene_name":"ankyrin repeat and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:16009]","synonyms":"ASB-4","biotype":"protein_coding","ncbi_id":"51666","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Multiple alternatively spliced transcript variants have been described for this gene but some of the full length sequences are not known. [provided by RefSeq, Jul 2008]","start":95478444,"end":95540232,"strand":1,"description":"ankyrin repeat and SOCS box containing 4 [Source:HGNC Symbol;Acc:HGNC:16009]"}, {"versioned_ensembl_gene_id":"ENSG00000113658.16","gene_symbol":"SMAD5","gene_name":"SMAD family member 5 [Source:HGNC Symbol;Acc:HGNC:6771]","synonyms":"MADH5,JV5-1,Dwfc","biotype":"protein_coding","ncbi_id":"4090","summary":"The protein encoded by this gene is involved in the transforming growth factor beta signaling pathway that results in an inhibition of the proliferation of hematopoietic progenitor cells. The encoded protein is activated by bone morphogenetic proteins type 1 receptor kinase, and may be involved in cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":136132845,"end":136188747,"strand":1,"description":"SMAD family member 5 [Source:HGNC Symbol;Acc:HGNC:6771]"}, {"versioned_ensembl_gene_id":"ENSG00000150995.18","gene_symbol":"ITPR1","gene_name":"inositol 1,4,5-trisphosphate receptor type 1 [Source:HGNC Symbol;Acc:HGNC:6180]","synonyms":"Insp3r1,ACV,SCA29,SCA16,SCA15,PPP1R94,IP3R1","biotype":"protein_coding","ncbi_id":"3708","summary":"This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]","start":4493348,"end":4847840,"strand":1,"description":"inositol 1,4,5-trisphosphate receptor type 1 [Source:HGNC Symbol;Acc:HGNC:6180]"}, {"versioned_ensembl_gene_id":"ENSG00000233635.2","gene_symbol":"AC015923.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63193930,"end":63339053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050344.8","gene_symbol":"NFE2L3","gene_name":"nuclear factor, erythroid 2 like 3 [Source:HGNC Symbol;Acc:HGNC:7783]","synonyms":"Nrf3","biotype":"protein_coding","ncbi_id":"9603","summary":"This gene encodes a member of the cap 'n' collar basic-region leucine zipper family of transcription factors. The encoded protein heterodimerizes with small musculoaponeurotic fibrosarcoma factors to bind antioxidant response elements in target genes. This protein is a membrane bound glycoprotein that is targeted to the endoplasmic reticulum and the nuclear envelope. Pseudogenes of this gene are found on chromosomes 16, 17, and 18. [provided by RefSeq, Mar 2009]","start":26152240,"end":26187125,"strand":1,"description":"nuclear factor, erythroid 2 like 3 [Source:HGNC Symbol;Acc:HGNC:7783]"}, {"versioned_ensembl_gene_id":"ENSG00000277349.1","gene_symbol":"AC133919.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90174062,"end":90175865,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260025.1","gene_symbol":"AC009414.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36354749,"end":36355114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071539.13","gene_symbol":"TRIP13","gene_name":"thyroid hormone receptor interactor 13 [Source:HGNC Symbol;Acc:HGNC:12307]","synonyms":"16E1BP","biotype":"protein_coding","ncbi_id":"9319","summary":"This gene encodes a protein that interacts with thyroid hormone receptors, also known as hormone-dependent transcription factors. The gene product interacts specifically with the ligand binding domain. This gene is one of several that may play a role in early-stage non-small cell lung cancer. [provided by RefSeq, Oct 2009]","start":892643,"end":919357,"strand":1,"description":"thyroid hormone receptor interactor 13 [Source:HGNC Symbol;Acc:HGNC:12307]"}, {"versioned_ensembl_gene_id":"ENSG00000135355.4","gene_symbol":"GJA10","gene_name":"gap junction protein alpha 10 [Source:HGNC Symbol;Acc:HGNC:16995]","synonyms":"CX62","biotype":"protein_coding","ncbi_id":"84694","summary":"Connexins, such as GJA10, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]","start":89894469,"end":89921760,"strand":1,"description":"gap junction protein alpha 10 [Source:HGNC Symbol;Acc:HGNC:16995]"}, {"versioned_ensembl_gene_id":"ENSG00000160172.10","gene_symbol":"FAM86C2P","gene_name":"family with sequence similarity 86 member C2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42392]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645332","summary":null,"start":67791648,"end":67805336,"strand":-1,"description":"family with sequence similarity 86 member C2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42392]"}, {"versioned_ensembl_gene_id":"ENSG00000214160.9","gene_symbol":"ALG3","gene_name":"ALG3, alpha-1,3- mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:23056]","synonyms":"CDGS4,NOT56L,Not56,D16Ertd36e","biotype":"protein_coding","ncbi_id":"10195","summary":"This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":184242301,"end":184249548,"strand":-1,"description":"ALG3, alpha-1,3- mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:23056]"}, {"versioned_ensembl_gene_id":"ENSG00000230269.6","gene_symbol":"LINC02525","gene_name":"long intergenic non-protein coding RNA 2525 [Source:HGNC Symbol;Acc:HGNC:53545]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507194","summary":null,"start":3182744,"end":3195756,"strand":-1,"description":"long intergenic non-protein coding RNA 2525 [Source:HGNC Symbol;Acc:HGNC:53545]"}, {"versioned_ensembl_gene_id":"ENSG00000231302.1","gene_symbol":"RPL36P2","gene_name":"ribosomal protein L36 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16570]","synonyms":"dJ530I15.5","biotype":"processed_pseudogene","ncbi_id":"140751","summary":null,"start":50620763,"end":50621077,"strand":1,"description":"ribosomal protein L36 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16570]"}, {"versioned_ensembl_gene_id":"ENSG00000167565.12","gene_symbol":"SERTAD3","gene_name":"SERTA domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17931]","synonyms":"RBT1","biotype":"protein_coding","ncbi_id":"29946","summary":"The protein encoded by this gene was identified in a yeast two-hybrid assay employing the second subunit of human replication protein A as bait. It is localized to the nucleus and its expression is significantly higher in cancer cell lines compared to normal cell lines. This protein has also been shown to be a strong transcriptional co-activator. Alternative splicing has been observed at this locus and two variants, both encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":40440844,"end":40444705,"strand":-1,"description":"SERTA domain containing 3 [Source:HGNC Symbol;Acc:HGNC:17931]"}, {"versioned_ensembl_gene_id":"ENSG00000237448.3","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31323725,"end":31324927,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000108424.9","gene_symbol":"KPNB1","gene_name":"karyopherin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6400]","synonyms":"NTF97,MGC2157,MGC2156,MGC2155,IPOB,IPO1,Impnb,IMB1","biotype":"protein_coding","ncbi_id":"3837","summary":"Nucleocytoplasmic transport, a signal- and energy-dependent process, takes place through nuclear pore complexes embedded in the nuclear envelope. The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor, a heterodimer of importin alpha and beta subunits also known as karyopherins. Importin alpha binds the NLS-containing cargo in the cytoplasm and importin beta docks the complex at the cytoplasmic side of the nuclear pore complex. In the presence of nucleoside triphosphates and the small GTP binding protein Ran, the complex moves into the nuclear pore complex and the importin subunits dissociate. Importin alpha enters the nucleoplasm with its passenger protein and importin beta remains at the pore. Interactions between importin beta and the FG repeats of nucleoporins are essential in translocation through the pore complex. The protein encoded by this gene is a member of the importin beta family. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":47649476,"end":47685505,"strand":1,"description":"karyopherin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6400]"}, {"versioned_ensembl_gene_id":"ENSG00000264247.1","gene_symbol":"LINC00909","gene_name":"long intergenic non-protein coding RNA 909 [Source:HGNC Symbol;Acc:HGNC:44331]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400657","summary":null,"start":74591774,"end":74598508,"strand":-1,"description":"long intergenic non-protein coding RNA 909 [Source:HGNC Symbol;Acc:HGNC:44331]"}, {"versioned_ensembl_gene_id":"ENSG00000204304.11","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"G17,PBX2MHC,HOX12","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32184741,"end":32190186,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000231694.1","gene_symbol":"AC244098.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149760779,"end":149760874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217404.2","gene_symbol":"RPS4XP9","gene_name":"ribosomal protein S4X pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35792]","synonyms":"RPS4P9","biotype":"processed_pseudogene","ncbi_id":"442257","summary":null,"start":126683036,"end":126683847,"strand":1,"description":"ribosomal protein S4X pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35792]"}, {"versioned_ensembl_gene_id":"ENSG00000271687.1","gene_symbol":"MTND5P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42272]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643031","summary":null,"start":100046977,"end":100048785,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42272]"}, {"versioned_ensembl_gene_id":"ENSG00000270230.1","gene_symbol":"MTND6P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075261","summary":null,"start":100046450,"end":100046970,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51978]"}, {"versioned_ensembl_gene_id":"ENSG00000231313.2","gene_symbol":"AC078875.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120914400,"end":120915123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266950.1","gene_symbol":"AC008752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9793621,"end":9802301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008382.15","gene_symbol":"MPND","gene_name":"MPN domain containing [Source:HGNC Symbol;Acc:HGNC:25934]","synonyms":"FLJ14981","biotype":"protein_coding","ncbi_id":"84954","summary":null,"start":4343527,"end":4360086,"strand":1,"description":"MPN domain containing [Source:HGNC Symbol;Acc:HGNC:25934]"}, {"versioned_ensembl_gene_id":"ENSG00000232442.1","gene_symbol":"MHENCR","gene_name":"melanoma highly expressed competing endogenous lncRNA for miR-425 and miR-489 [Source:HGNC Symbol;Acc:HGNC:53110]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505771","summary":null,"start":63627227,"end":63628824,"strand":1,"description":"melanoma highly expressed competing endogenous lncRNA for miR-425 and miR-489 [Source:HGNC Symbol;Acc:HGNC:53110]"}, {"versioned_ensembl_gene_id":"ENSG00000267938.1","gene_symbol":"EIF1P6","gene_name":"eukaryotic translation initiation factor 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49619]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480277","summary":null,"start":4347780,"end":4349061,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49619]"}, {"versioned_ensembl_gene_id":"ENSG00000265763.3","gene_symbol":"ZNF488","gene_name":"zinc finger protein 488 [Source:HGNC Symbol;Acc:HGNC:23535]","synonyms":"FLJ32104","biotype":"protein_coding","ncbi_id":"118738","summary":null,"start":47365496,"end":47384273,"strand":-1,"description":"zinc finger protein 488 [Source:HGNC Symbol;Acc:HGNC:23535]"}, {"versioned_ensembl_gene_id":"ENSG00000141367.11","gene_symbol":"CLTC","gene_name":"clathrin heavy chain [Source:HGNC Symbol;Acc:HGNC:2092]","synonyms":"Hc,CLTCL2","biotype":"protein_coding","ncbi_id":"1213","summary":" Clathrin is a major protein component of the cytoplasmic face of intracellular organelles, called coated vesicles and coated pits. These specialized organelles are involved in the intracellular trafficking of receptors and endocytosis of a variety of macromolecules. The basic subunit of the clathrin coat is composed of three heavy chains and three light chains. [provided by RefSeq, Jul 2008]","start":59619689,"end":59696956,"strand":1,"description":"clathrin heavy chain [Source:HGNC Symbol;Acc:HGNC:2092]"}, {"versioned_ensembl_gene_id":"ENSG00000203943.8","gene_symbol":"SAMD13","gene_name":"sterile alpha motif domain containing 13 [Source:HGNC Symbol;Acc:HGNC:24582]","synonyms":null,"biotype":"protein_coding","ncbi_id":"148418","summary":null,"start":84298366,"end":84389957,"strand":1,"description":"sterile alpha motif domain containing 13 [Source:HGNC Symbol;Acc:HGNC:24582]"}, {"versioned_ensembl_gene_id":"ENSG00000167613.15","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54351384,"end":54370558,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000257747.1","gene_symbol":"LINC02426","gene_name":"long intergenic non-protein coding RNA 2426 [Source:HGNC Symbol;Acc:HGNC:53357]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928449","summary":null,"start":81953719,"end":81993133,"strand":1,"description":"long intergenic non-protein coding RNA 2426 [Source:HGNC Symbol;Acc:HGNC:53357]"}, {"versioned_ensembl_gene_id":"ENSG00000280798.1","gene_symbol":"LINC00294","gene_name":"long intergenic non-protein coding RNA 294 [Source:HGNC Symbol;Acc:HGNC:27456]","synonyms":"NCRNA00294","biotype":"lincRNA","ncbi_id":"283267","summary":null,"start":33076149,"end":33079454,"strand":1,"description":"long intergenic non-protein coding RNA 294 [Source:HGNC Symbol;Acc:HGNC:27456]"}, {"versioned_ensembl_gene_id":"ENSG00000213713.3","gene_symbol":"PIGCP1","gene_name":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8961]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5280","summary":null,"start":33075566,"end":33076460,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8961]"}, {"versioned_ensembl_gene_id":"ENSG00000060069.16","gene_symbol":"CTDP1","gene_name":"CTD phosphatase subunit 1 [Source:HGNC Symbol;Acc:HGNC:2498]","synonyms":"FCP1","biotype":"protein_coding","ncbi_id":"9150","summary":"This gene encodes a protein which interacts with the carboxy-terminus of the RAP74 subunit of transcription initiation factor TFIIF, and functions as a phosphatase that processively dephosphorylates the C-terminus of POLR2A (a subunit of RNA polymerase II), making it available for initiation of gene expression. Mutations in this gene are associated with congenital cataracts, facial dysmorphism and neuropathy syndrome (CCFDN). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":79679801,"end":79756623,"strand":1,"description":"CTD phosphatase subunit 1 [Source:HGNC Symbol;Acc:HGNC:2498]"}, {"versioned_ensembl_gene_id":"ENSG00000124134.8","gene_symbol":"KCNS1","gene_name":"potassium voltage-gated channel modifier subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:6300]","synonyms":"Kv9.1","biotype":"protein_coding","ncbi_id":"3787","summary":"Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the potassium channel family. [provided by RefSeq, Jul 2008]","start":45092310,"end":45101112,"strand":-1,"description":"potassium voltage-gated channel modifier subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:6300]"}, {"versioned_ensembl_gene_id":"ENSG00000137876.9","gene_symbol":"RSL24D1","gene_name":"ribosomal L24 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18479]","synonyms":"RPL24L,RPL24,L30,HRP-L30-iso,C15orf15","biotype":"protein_coding","ncbi_id":"51187","summary":"This gene encodes a protein sharing a low level of sequence similarity with human ribosomal protein L24. Although this gene has been referred to as RPL24, L30, and 60S ribosomal protein L30 isolog in the sequence databases, it is distinct from the human genes officially named RPL24 (which itself has been referred to as ribosomal protein L30) and RPL30. The protein encoded by this gene localizes to the nucleolus and is thought to play a role in the biogenesis of the 60S ribosomal subunit. The precise function of this gene is currently unknown. This gene utilizes alternative polyadenylation signals and has multiple pseudogenes. [provided by RefSeq, Jul 2012]","start":55180806,"end":55197067,"strand":-1,"description":"ribosomal L24 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18479]"}, {"versioned_ensembl_gene_id":"ENSG00000230461.8","gene_symbol":"PROX1-AS1","gene_name":"PROX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43656]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100505832","summary":null,"start":213817751,"end":213988508,"strand":-1,"description":"PROX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43656]"}, {"versioned_ensembl_gene_id":"ENSG00000169688.10","gene_symbol":"MT1B","gene_name":"metallothionein 1B [Source:HGNC Symbol;Acc:HGNC:7394]","synonyms":"MT1Q,MT1","biotype":"protein_coding","ncbi_id":"4490","summary":"The protein encoded by this gene binds heavy metals and protects against toxicity from heavy metal ions. This gene is found in a cluster of similar genes on chromosome 16. [provided by RefSeq, Jul 2016]","start":56651899,"end":56653204,"strand":1,"description":"metallothionein 1B [Source:HGNC Symbol;Acc:HGNC:7394]"}, {"versioned_ensembl_gene_id":"ENSG00000130208.9","gene_symbol":"APOC1","gene_name":"apolipoprotein C1 [Source:HGNC Symbol;Acc:HGNC:607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341","summary":"This gene encodes a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. The encoded protein plays a central role in high density lipoprotein (HDL) and very low density lipoprotein (VLDL) metabolism. This protein has also been shown to inhibit cholesteryl ester transfer protein in plasma. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":44914247,"end":44919349,"strand":1,"description":"apolipoprotein C1 [Source:HGNC Symbol;Acc:HGNC:607]"}, {"versioned_ensembl_gene_id":"ENSG00000237329.2","gene_symbol":"AL356320.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31036734,"end":31037240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184523.3","gene_symbol":"PTGER4P2","gene_name":"prostaglandin E receptor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5736","summary":null,"start":62843919,"end":62844170,"strand":1,"description":"prostaglandin E receptor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9598]"}, {"versioned_ensembl_gene_id":"ENSG00000124782.19","gene_symbol":"RREB1","gene_name":"ras responsive element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10449]","synonyms":"HNT","biotype":"protein_coding","ncbi_id":"6239","summary":"The protein encoded by this gene is a zinc finger transcription factor that binds to RAS-responsive elements (RREs) of gene promoters. It has been shown that the calcitonin gene promoter contains an RRE and that the encoded protein binds there and increases expression of calcitonin, which may be involved in Ras/Raf-mediated cell differentiation. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":7107597,"end":7251980,"strand":1,"description":"ras responsive element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10449]"}, {"versioned_ensembl_gene_id":"ENSG00000126953.5","gene_symbol":"TIMM8A","gene_name":"translocase of inner mitochondrial membrane 8A [Source:HGNC Symbol;Acc:HGNC:11817]","synonyms":"MTS,DFN1,DDP","biotype":"protein_coding","ncbi_id":"1678","summary":"This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009]","start":101345661,"end":101349196,"strand":-1,"description":"translocase of inner mitochondrial membrane 8A [Source:HGNC Symbol;Acc:HGNC:11817]"}, {"versioned_ensembl_gene_id":"ENSG00000166595.11","gene_symbol":"FAM96B","gene_name":"family with sequence similarity 96 member B [Source:HGNC Symbol;Acc:HGNC:24261]","synonyms":"MIP18,CIA2B,CGI-128","biotype":"protein_coding","ncbi_id":"51647","summary":null,"start":66932055,"end":66934423,"strand":-1,"description":"family with sequence similarity 96 member B [Source:HGNC Symbol;Acc:HGNC:24261]"}, {"versioned_ensembl_gene_id":"ENSG00000078098.13","gene_symbol":"FAP","gene_name":"fibroblast activation protein alpha [Source:HGNC Symbol;Acc:HGNC:3590]","synonyms":"DPPIV","biotype":"protein_coding","ncbi_id":"2191","summary":"The protein encoded by this gene is a homodimeric integral membrane gelatinase belonging to the serine protease family. It is selectively expressed in reactive stromal fibroblasts of epithelial cancers, granulation tissue of healing wounds, and malignant cells of bone and soft tissue sarcomas. This protein is thought to be involved in the control of fibroblast growth or epithelial-mesenchymal interactions during development, tissue repair, and epithelial carcinogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":162170684,"end":162245151,"strand":-1,"description":"fibroblast activation protein alpha [Source:HGNC Symbol;Acc:HGNC:3590]"}, {"versioned_ensembl_gene_id":"ENSG00000229361.5","gene_symbol":"UBTFL7","gene_name":"upstream binding transcription factor, RNA polymerase I-like 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646759","summary":null,"start":49081907,"end":49083097,"strand":1,"description":"upstream binding transcription factor, RNA polymerase I-like 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35404]"}, {"versioned_ensembl_gene_id":"ENSG00000273214.1","gene_symbol":"AL031587.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38043230,"end":38043920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213703.2","gene_symbol":"AL138847.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62641122,"end":62641667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162571.13","gene_symbol":"TTLL10","gene_name":"tubulin tyrosine ligase like 10 [Source:HGNC Symbol;Acc:HGNC:26693]","synonyms":"TTLL5,FLJ36119","biotype":"protein_coding","ncbi_id":"254173","summary":null,"start":1173884,"end":1197935,"strand":1,"description":"tubulin tyrosine ligase like 10 [Source:HGNC Symbol;Acc:HGNC:26693]"}, {"versioned_ensembl_gene_id":"ENSG00000234527.1","gene_symbol":"PCDH9-AS1","gene_name":"PCDH9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39897]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874065","summary":null,"start":66303871,"end":66323561,"strand":1,"description":"PCDH9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39897]"}, {"versioned_ensembl_gene_id":"ENSG00000184612.8","gene_symbol":"RPL7P26","gene_name":"ribosomal protein L7 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728380","summary":null,"start":17530899,"end":17531652,"strand":-1,"description":"ribosomal protein L7 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36630]"}, {"versioned_ensembl_gene_id":"ENSG00000271897.1","gene_symbol":"AL357518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11607552,"end":11607981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108242.12","gene_symbol":"CYP2C18","gene_name":"cytochrome P450 family 2 subfamily C member 18 [Source:HGNC Symbol;Acc:HGNC:2620]","synonyms":"P450IIC17,CYP2C17,CYP2C,CPCI","biotype":"protein_coding","ncbi_id":"1562","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum but its specific substrate has not yet been determined. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. An additional gene, CYP2C17, was once thought to exist; however, CYP2C17 is now considered an artefact based on a chimera of CYP2C18 and CYP2C19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":94683621,"end":94736190,"strand":1,"description":"cytochrome P450 family 2 subfamily C member 18 [Source:HGNC Symbol;Acc:HGNC:2620]"}, {"versioned_ensembl_gene_id":"ENSG00000276490.1","gene_symbol":"AL583836.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":94688154,"end":94853073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259668.5","gene_symbol":"AC066613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51457286,"end":51460582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268447.5","gene_symbol":"SSX2B","gene_name":"SSX family member 2B [Source:HGNC Symbol;Acc:HGNC:22263]","synonyms":"CT5.2b","biotype":"protein_coding","ncbi_id":"727837","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX1 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. This gene also has an identical duplicate, GeneID: 6757, located about 45 kb upstream in the opposite orientation on chromosome X. [provided by RefSeq, Jul 2013]","start":52751132,"end":52790305,"strand":1,"description":"SSX family member 2B [Source:HGNC Symbol;Acc:HGNC:22263]"}, {"versioned_ensembl_gene_id":"ENSG00000231558.11","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-DNA,HLA-D0-alpha,HLA-DZA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":33157934,"end":33163367,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000214051.3","gene_symbol":"ARF4P3","gene_name":"ADP ribosylation factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390423","summary":null,"start":100756551,"end":100757059,"strand":-1,"description":"ADP ribosylation factor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32380]"}, {"versioned_ensembl_gene_id":"ENSG00000166508.17","gene_symbol":"MCM7","gene_name":"minichromosome maintenance complex component 7 [Source:HGNC Symbol;Acc:HGNC:6950]","synonyms":"PPP1R104,MCM2,CDC47","biotype":"protein_coding","ncbi_id":"4176","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 4 and 6 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. Cyclin D1-dependent kinase, CDK4, is found to associate with this protein, and may regulate the binding of this protein with the tumorsuppressor protein RB1/RB. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":100092728,"end":100101940,"strand":-1,"description":"minichromosome maintenance complex component 7 [Source:HGNC Symbol;Acc:HGNC:6950]"}, {"versioned_ensembl_gene_id":"ENSG00000069275.12","gene_symbol":"NUCKS1","gene_name":"nuclear casein kinase and cyclin dependent kinase substrate 1 [Source:HGNC Symbol;Acc:HGNC:29923]","synonyms":"NUCKS","biotype":"protein_coding","ncbi_id":"64710","summary":"This gene encodes a nuclear protein that is highly conserved in vertebrates. The conserved regions of the protein contain several consensus phosphorylation sites for casein kinase II and cyclin-dependent kinases, two putative nuclear localization signals, and a basic DNA-binding domain. It is phosphorylated in vivo by Cdk1 during mitosis of the cell cycle. [provided by RefSeq, Aug 2010]","start":205712819,"end":205750276,"strand":-1,"description":"nuclear casein kinase and cyclin dependent kinase substrate 1 [Source:HGNC Symbol;Acc:HGNC:29923]"}, {"versioned_ensembl_gene_id":"ENSG00000236511.1","gene_symbol":"LINC01231","gene_name":"long intergenic non-protein coding RNA 1231 [Source:HGNC Symbol;Acc:HGNC:49688]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929247","summary":null,"start":3181589,"end":3198517,"strand":1,"description":"long intergenic non-protein coding RNA 1231 [Source:HGNC Symbol;Acc:HGNC:49688]"}, {"versioned_ensembl_gene_id":"ENSG00000241890.1","gene_symbol":"AC105137.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75388267,"end":75388828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236236.9","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"XB,TNXB2,XBS,TNXB1,TNXBS","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32033807,"end":32060653,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000231184.3","gene_symbol":"FAM58DP","gene_name":"family with sequence similarity 58 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:42022]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421566","summary":null,"start":19382454,"end":19383072,"strand":1,"description":"family with sequence similarity 58 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:42022]"}, {"versioned_ensembl_gene_id":"ENSG00000261407.1","gene_symbol":"AC013565.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89087078,"end":89088267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236927.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29306763,"end":29307728,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000265791.1","gene_symbol":"AC127024.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30781493,"end":30782221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227512.1","gene_symbol":"AL592301.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136542881,"end":136543835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278622.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"LENG5,LENG5,SEN34,SEN34,SEN34L,SEN34L","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190368,"end":54194965,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000101654.17","gene_symbol":"RNMT","gene_name":"RNA guanine-7 methyltransferase [Source:HGNC Symbol;Acc:HGNC:10075]","synonyms":"RG7MT1","biotype":"protein_coding","ncbi_id":"8731","summary":null,"start":13726660,"end":13764558,"strand":1,"description":"RNA guanine-7 methyltransferase [Source:HGNC Symbol;Acc:HGNC:10075]"}, {"versioned_ensembl_gene_id":"ENSG00000152332.15","gene_symbol":"UHMK1","gene_name":"U2AF homology motif kinase 1 [Source:HGNC Symbol;Acc:HGNC:19683]","synonyms":"KIS,Kist","biotype":"protein_coding","ncbi_id":"127933","summary":"The gene encodes a serine/threonine protein kinase that promotes cell cycle progression through G1 by phosphorylation of the cyclin-dependent kinase inhibitor 1B (p27Kip1), which causes nuclear export and degradation. The encoded protein is also thought to function in the adult nervous system and the gene has been associated with schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":162497251,"end":162529629,"strand":1,"description":"U2AF homology motif kinase 1 [Source:HGNC Symbol;Acc:HGNC:19683]"}, {"versioned_ensembl_gene_id":"ENSG00000234224.2","gene_symbol":"TMEM229A","gene_name":"transmembrane protein 229A [Source:HGNC Symbol;Acc:HGNC:37279]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730130","summary":null,"start":124030916,"end":124033023,"strand":-1,"description":"transmembrane protein 229A [Source:HGNC Symbol;Acc:HGNC:37279]"}, {"versioned_ensembl_gene_id":"ENSG00000234217.2","gene_symbol":"RBPJP7","gene_name":"RBPJ pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133122","summary":null,"start":62601226,"end":62602672,"strand":1,"description":"RBPJ pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37487]"}, {"versioned_ensembl_gene_id":"ENSG00000160593.18","gene_symbol":"JAML","gene_name":"junction adhesion molecule like [Source:HGNC Symbol;Acc:HGNC:19084]","synonyms":"Gm638,AMICA1,AMICA","biotype":"protein_coding","ncbi_id":"120425","summary":null,"start":118193740,"end":118225094,"strand":-1,"description":"junction adhesion molecule like [Source:HGNC Symbol;Acc:HGNC:19084]"}, {"versioned_ensembl_gene_id":"ENSG00000132781.17","gene_symbol":"MUTYH","gene_name":"mutY DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:7527]","synonyms":"MYH","biotype":"protein_coding","ncbi_id":"4595","summary":"This gene encodes a DNA glycosylase involved in oxidative DNA damage repair. The enzyme excises adenine bases from the DNA backbone at sites where adenine is inappropriately paired with guanine, cytosine, or 8-oxo-7,8-dihydroguanine, a major oxidatively damaged DNA lesion. The protein is localized to the nucleus and mitochondria. This gene product is thought to play a role in signaling apoptosis by the introduction of single-strand breaks following oxidative damage. Mutations in this gene result in heritable predisposition to colorectal cancer, termed MUTYH-associated polyposis (MAP). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2017]","start":45329163,"end":45340470,"strand":-1,"description":"mutY DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:7527]"}, {"versioned_ensembl_gene_id":"ENSG00000215425.11","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"BAT1,UAP56,D6S81E","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31520488,"end":31536841,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000243547.1","gene_symbol":"HNRNPKP4","gene_name":"heterogeneous nuclear ribonucleoprotein K pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644063","summary":null,"start":96349554,"end":96350939,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein K pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42377]"}, {"versioned_ensembl_gene_id":"ENSG00000214293.8","gene_symbol":"APTR","gene_name":"Alu-mediated CDKN1A/p21 transcriptional regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44173]","synonyms":"RSBN1L-AS1","biotype":"lincRNA","ncbi_id":"100505854","summary":null,"start":77657660,"end":77696265,"strand":-1,"description":"Alu-mediated CDKN1A/p21 transcriptional regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44173]"}, {"versioned_ensembl_gene_id":"ENSG00000281153.1","gene_symbol":"AC136352.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21382467,"end":21382926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176593.7","gene_symbol":"AC008969.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":58002061,"end":58011232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139160.13","gene_symbol":"ETFBKMT","gene_name":"electron transfer flavoprotein beta subunit lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:28739]","synonyms":"MGC50559,METTL20,DKFZp451L235,C12orf72","biotype":"protein_coding","ncbi_id":"254013","summary":null,"start":31647160,"end":31673114,"strand":1,"description":"electron transfer flavoprotein beta subunit lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:28739]"}, {"versioned_ensembl_gene_id":"ENSG00000141959.16","gene_symbol":"PFKL","gene_name":"phosphofructokinase, liver type [Source:HGNC Symbol;Acc:HGNC:8876]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5211","summary":"This gene encodes the liver (L) subunit of an enzyme that catalyzes the conversion of D-fructose 6-phosphate to D-fructose 1,6-bisphosphate, which is a key step in glucose metabolism (glycolysis). This enzyme is a tetramer that may be composed of different subunits encoded by distinct genes in different tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":44300051,"end":44327376,"strand":1,"description":"phosphofructokinase, liver type [Source:HGNC Symbol;Acc:HGNC:8876]"}, {"versioned_ensembl_gene_id":"ENSG00000131187.9","gene_symbol":"F12","gene_name":"coagulation factor XII [Source:HGNC Symbol;Acc:HGNC:3530]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2161","summary":"This gene encodes coagulation factor XII which circulates in blood as a zymogen. This single chain zymogen is converted to a two-chain serine protease with an heavy chain (alpha-factor XIIa) and a light chain. The heavy chain contains two fibronectin-type domains, two epidermal growth factor (EGF)-like domains, a kringle domain and a proline-rich domain, whereas the light chain contains only a catalytic domain. On activation, further cleavages takes place in the heavy chain, resulting in the production of beta-factor XIIa light chain and the alpha-factor XIIa light chain becomes beta-factor XIIa heavy chain. Prekallikrein is cleaved by factor XII to form kallikrein, which then cleaves factor XII first to alpha-factor XIIa and then to beta-factor XIIa. The active factor XIIa participates in the initiation of blood coagulation, fibrinolysis, and the generation of bradykinin and angiotensin. It activates coagulation factors VII and XI. Defects in this gene do not cause any clinical symptoms and the sole effect is that whole-blood clotting time is prolonged. [provided by RefSeq, Jul 2008]","start":177402140,"end":177409576,"strand":-1,"description":"coagulation factor XII [Source:HGNC Symbol;Acc:HGNC:3530]"}, {"versioned_ensembl_gene_id":"ENSG00000233730.1","gene_symbol":"LINC01765","gene_name":"long intergenic non-protein coding RNA 1765 [Source:HGNC Symbol;Acc:HGNC:52555]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378916","summary":null,"start":115099672,"end":115102658,"strand":1,"description":"long intergenic non-protein coding RNA 1765 [Source:HGNC Symbol;Acc:HGNC:52555]"}, {"versioned_ensembl_gene_id":"ENSG00000279050.1","gene_symbol":"PWAR1","gene_name":"Prader Willi/Angelman region RNA 1 [Source:HGNC Symbol;Acc:HGNC:30089]","synonyms":"PAR1,PAR-1","biotype":"TEC","ncbi_id":"145624","summary":null,"start":25135642,"end":25138055,"strand":1,"description":"Prader Willi/Angelman region RNA 1 [Source:HGNC Symbol;Acc:HGNC:30089]"}, {"versioned_ensembl_gene_id":"ENSG00000070010.18","gene_symbol":"UFD1","gene_name":"ubiquitin recognition factor in ER associated degradation 1 [Source:HGNC Symbol;Acc:HGNC:12520]","synonyms":"UFD1L","biotype":"protein_coding","ncbi_id":"7353","summary":"The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Jun 2009]","start":19449910,"end":19479215,"strand":-1,"description":"ubiquitin recognition factor in ER associated degradation 1 [Source:HGNC Symbol;Acc:HGNC:12520]"}, {"versioned_ensembl_gene_id":"ENSG00000236829.9","gene_symbol":"Z97634.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":382097,"end":392960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169302.14","gene_symbol":"STK32A","gene_name":"serine/threonine kinase 32A [Source:HGNC Symbol;Acc:HGNC:28317]","synonyms":"MGC22688,YANK1","biotype":"protein_coding","ncbi_id":"202374","summary":null,"start":147234963,"end":147387852,"strand":1,"description":"serine/threonine kinase 32A [Source:HGNC Symbol;Acc:HGNC:28317]"}, {"versioned_ensembl_gene_id":"ENSG00000259669.5","gene_symbol":"AC084759.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53947624,"end":53976908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219747.1","gene_symbol":"AL133260.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151099529,"end":151099933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218996.1","gene_symbol":"ARL4AP5","gene_name":"ADP ribosylation factor like GTPase 4A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101928788","summary":null,"start":150934968,"end":150935566,"strand":1,"description":"ADP ribosylation factor like GTPase 4A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52374]"}, {"versioned_ensembl_gene_id":"ENSG00000273366.1","gene_symbol":"Z83851.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42278188,"end":42278846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242628.5","gene_symbol":"AC009228.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24214381,"end":24221516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216824.2","gene_symbol":"ZNF736P10Y","gene_name":"zinc finger protein 736 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:38410]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419727","summary":null,"start":8418791,"end":8419900,"strand":-1,"description":"zinc finger protein 736 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:38410]"}, {"versioned_ensembl_gene_id":"ENSG00000276758.1","gene_symbol":"AC245884.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54296194,"end":54296252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047578.12","gene_symbol":"KIAA0556","gene_name":"KIAA0556 [Source:HGNC Symbol;Acc:HGNC:29068]","synonyms":"KATNIP,JBTS26","biotype":"protein_coding","ncbi_id":"23247","summary":"This gene encodes a novel, evolutionarily conserved, ciliary protein. In human hTERT-RPE1 cells, the protein is found at the base of cilia, decorating the ciliary axoneme, and enriched at the ciliary tip. The protein binds to microtubules in vitro and regulates their stability when it is overexpressed. A null mutation in this gene has been associated with Joubert syndrome, a recessive disorder that is characterized by a distinctive mid-hindbrain and cerebellar malformation and is also often associated with wider ciliopathy symptoms. Consistently, in a serum-starvation ciliogenesis assay, human fibroblast cells derived from patients with the mutation display a reduced number of ciliated cells with abnormally long cilia. [provided by RefSeq, Feb 2016]","start":27550133,"end":27780369,"strand":1,"description":"KIAA0556 [Source:HGNC Symbol;Acc:HGNC:29068]"}, {"versioned_ensembl_gene_id":"ENSG00000149575.5","gene_symbol":"SCN2B","gene_name":"sodium voltage-gated channel beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:10589]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6327","summary":"The protein encoded by this gene is the beta 2 subunit of the type II voltage-gated sodium channel. The encoded protein is involved in cell-cell adhesion and cell migration. Defects in this gene can be a cause of Brugada Syndrome, atrial fibrillation, or sudden infant death syndrome. [provided by RefSeq, Jul 2015]","start":118161951,"end":118176673,"strand":-1,"description":"sodium voltage-gated channel beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:10589]"}, {"versioned_ensembl_gene_id":"ENSG00000251618.1","gene_symbol":"AC007322.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21895394,"end":21897559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238161.1","gene_symbol":"OR7E117P","gene_name":"olfactory receptor family 7 subfamily E member 117 pseudogene [Source:HGNC Symbol;Acc:HGNC:15303]","synonyms":"OST716","biotype":"unprocessed_pseudogene","ncbi_id":"399857","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3599595,"end":3600706,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 117 pseudogene [Source:HGNC Symbol;Acc:HGNC:15303]"}, {"versioned_ensembl_gene_id":"ENSG00000182048.11","gene_symbol":"TRPC2","gene_name":"transient receptor potential cation channel subfamily C member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12334]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"7221","summary":null,"start":3609901,"end":3637559,"strand":1,"description":"transient receptor potential cation channel subfamily C member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12334]"}, {"versioned_ensembl_gene_id":"ENSG00000255655.1","gene_symbol":"AC007570.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109445410,"end":109447497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235534.1","gene_symbol":"FECHP1","gene_name":"ferrochelatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3648]","synonyms":"FECHP","biotype":"processed_pseudogene","ncbi_id":"2236","summary":null,"start":34872641,"end":34873854,"strand":1,"description":"ferrochelatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3648]"}, {"versioned_ensembl_gene_id":"ENSG00000197299.10","gene_symbol":"BLM","gene_name":"Bloom syndrome RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:1058]","synonyms":"RECQL3,RECQ2,BS","biotype":"protein_coding","ncbi_id":"641","summary":"The Bloom syndrome is an autosomal recessive disorder characterized by growth deficiency, microcephaly and immunodeficiency among others. It is caused by homozygous or compound heterozygous mutation in the gene encoding DNA helicase RecQ protein on chromosome 15q26. This Bloom-associated helicase unwinds a variety of DNA substrates including Holliday junction, and is involved in several pathways contributing to the maintenance of genome stability. Identification of pathogenic Bloom variants is required for heterozygote testing in at-risk families. [provided by RefSeq, May 2020]","start":90717327,"end":90816165,"strand":1,"description":"Bloom syndrome RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:1058]"}, {"versioned_ensembl_gene_id":"ENSG00000248148.1","gene_symbol":"AC114954.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45035199,"end":45098647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231989.4","gene_symbol":"PPP1R2P3","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16318]","synonyms":"MGC87149","biotype":"protein_coding","ncbi_id":"153743","summary":null,"start":156850538,"end":156852528,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16318]"}, {"versioned_ensembl_gene_id":"ENSG00000243414.5","gene_symbol":"TICAM2","gene_name":"toll like receptor adaptor molecule 2 [Source:HGNC Symbol;Acc:HGNC:21354]","synonyms":"TIRP,TICAM-2,TRAM","biotype":"protein_coding","ncbi_id":"353376","summary":"TIRP is a Toll/interleukin-1 receptor (IL1R; MIM 147810) (TIR) domain-containing adaptor protein involved in Toll receptor signaling (see TLR4; MIM 603030).[supplied by OMIM, Apr 2004]","start":115578650,"end":115602479,"strand":-1,"description":"toll like receptor adaptor molecule 2 [Source:HGNC Symbol;Acc:HGNC:21354]"}, {"versioned_ensembl_gene_id":"ENSG00000227283.1","gene_symbol":"RPL35AP12","gene_name":"ribosomal protein L35a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36068]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271316","summary":null,"start":163382179,"end":163382516,"strand":1,"description":"ribosomal protein L35a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36068]"}, {"versioned_ensembl_gene_id":"ENSG00000186462.8","gene_symbol":"NAP1L2","gene_name":"nucleosome assembly protein 1 like 2 [Source:HGNC Symbol;Acc:HGNC:7638]","synonyms":"MGC26243,BPX","biotype":"protein_coding","ncbi_id":"4674","summary":"The protein encoded by this intronless gene is a member of the nucleosome assembly protein (NAP) family. The encoded protein represents a class of tissue-specific factors that interact with chromatin to regulate neuronal cell proliferation. [provided by RefSeq, Jan 2011]","start":73212299,"end":73214848,"strand":-1,"description":"nucleosome assembly protein 1 like 2 [Source:HGNC Symbol;Acc:HGNC:7638]"}, {"versioned_ensembl_gene_id":"ENSG00000071655.17","gene_symbol":"MBD3","gene_name":"methyl-CpG binding domain protein 3 [Source:HGNC Symbol;Acc:HGNC:6918]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53615","summary":"DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. This gene belongs to a family of nuclear proteins which are characterized by the presence of a methyl-CpG binding domain (MBD). The encoded protein is a subunit of the NuRD, a multisubunit complex containing nucleosome remodeling and histone deacetylase activities. Unlike the other family members, the encoded protein is not capable of binding to methylated DNA. The protein mediates the association of metastasis-associated protein 2 with the core histone deacetylase complex. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":1573596,"end":1592801,"strand":-1,"description":"methyl-CpG binding domain protein 3 [Source:HGNC Symbol;Acc:HGNC:6918]"}, {"versioned_ensembl_gene_id":"ENSG00000104356.10","gene_symbol":"POP1","gene_name":"POP1 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:30129]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10940","summary":"This gene encodes the protein subunit of two different small nucleolar ribonucleoprotein complexes: the endoribonuclease for mitochondrial RNA processing complex and the ribonuclease P complex. The encoded protein is a ribonuclease that localizes to the nucleus and functions in pre-RNA processing. This protein is also an autoantigen in patients suffering from connective tissue diseases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":98117297,"end":98159834,"strand":1,"description":"POP1 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:30129]"}, {"versioned_ensembl_gene_id":"ENSG00000196534.5","gene_symbol":"OR9K1P","gene_name":"olfactory receptor family 9 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15338]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"121360","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55113077,"end":55118632,"strand":1,"description":"olfactory receptor family 9 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15338]"}, {"versioned_ensembl_gene_id":"ENSG00000279009.1","gene_symbol":"AC005943.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1576939,"end":1577086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110906.12","gene_symbol":"KCTD10","gene_name":"potassium channel tetramerization domain containing 10 [Source:HGNC Symbol;Acc:HGNC:23236]","synonyms":"MSTP028,BTBD28","biotype":"protein_coding","ncbi_id":"83892","summary":"The protein encoded by this gene binds proliferating cell nuclear antigen (PCNA) and may be involved in DNA synthesis and cell proliferation. In addition, the encoded protein may be a tumor suppressor. Several protein-coding and non-protein coding transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":109448656,"end":109477544,"strand":-1,"description":"potassium channel tetramerization domain containing 10 [Source:HGNC Symbol;Acc:HGNC:23236]"}, {"versioned_ensembl_gene_id":"ENSG00000231970.1","gene_symbol":"AL355490.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97401115,"end":97419524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080608.9","gene_symbol":"PUM3","gene_name":"pumilio RNA binding family member 3 [Source:HGNC Symbol;Acc:HGNC:29676]","synonyms":"XTP5,PUF6,PEN,KIAA0020,hPUF-A,HA-8","biotype":"protein_coding","ncbi_id":"9933","summary":null,"start":2720469,"end":2844241,"strand":-1,"description":"pumilio RNA binding family member 3 [Source:HGNC Symbol;Acc:HGNC:29676]"}, {"versioned_ensembl_gene_id":"ENSG00000253658.5","gene_symbol":"LINC01592","gene_name":"long intergenic non-protein coding RNA 1592 [Source:HGNC Symbol;Acc:HGNC:51557]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505718","summary":null,"start":68911803,"end":69104190,"strand":-1,"description":"long intergenic non-protein coding RNA 1592 [Source:HGNC Symbol;Acc:HGNC:51557]"}, {"versioned_ensembl_gene_id":"ENSG00000233705.6","gene_symbol":"SLC26A4-AS1","gene_name":"SLC26A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:22385]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"286002","summary":null,"start":107653968,"end":107662151,"strand":-1,"description":"SLC26A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:22385]"}, {"versioned_ensembl_gene_id":"ENSG00000242147.1","gene_symbol":"AL365356.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5594991,"end":5596118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220960.1","gene_symbol":"AL079342.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89059628,"end":89060109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111726.12","gene_symbol":"CMAS","gene_name":"cytidine monophosphate N-acetylneuraminic acid synthetase [Source:HGNC Symbol;Acc:HGNC:18290]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55907","summary":"This gene encodes an enzyme that converts N-acetylneuraminic acid (NeuNAc) to cytidine 5'-monophosphate N-acetylneuraminic acid (CMP-NeuNAc). This process is important in the formation of sialylated glycoprotein and glycolipids. This modification plays a role in cell-cell communications and immune responses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":22046174,"end":22065674,"strand":1,"description":"cytidine monophosphate N-acetylneuraminic acid synthetase [Source:HGNC Symbol;Acc:HGNC:18290]"}, {"versioned_ensembl_gene_id":"ENSG00000163631.16","gene_symbol":"ALB","gene_name":"albumin [Source:HGNC Symbol;Acc:HGNC:399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"213","summary":"This gene encodes the most abundant protein in human blood. This protein functions in the regulation of blood plasma colloid osmotic pressure and acts as a carrier protein for a wide range of endogenous molecules including hormones, fatty acids, and metabolites, as well as exogenous drugs. Additionally, this protein exhibits an esterase-like activity with broad substrate specificity. The encoded preproprotein is proteolytically processed to generate the mature protein. A peptide derived from this protein, EPI-X4, is an endogenous inhibitor of the CXCR4 chemokine receptor. [provided by RefSeq, Jul 2016]","start":73397114,"end":73421412,"strand":1,"description":"albumin [Source:HGNC Symbol;Acc:HGNC:399]"}, {"versioned_ensembl_gene_id":"ENSG00000229980.4","gene_symbol":"TOB1-AS1","gene_name":"TOB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44340]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"400604","summary":null,"start":50866679,"end":50909737,"strand":1,"description":"TOB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44340]"}, {"versioned_ensembl_gene_id":"ENSG00000280597.1","gene_symbol":"AF186996.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125734326,"end":125735208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279578.1","gene_symbol":"AC004899.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48847766,"end":48851625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243521.2","gene_symbol":"RPL5P33","gene_name":"ribosomal protein L5 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36703]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130929","summary":null,"start":50847950,"end":50849270,"strand":1,"description":"ribosomal protein L5 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36703]"}, {"versioned_ensembl_gene_id":"ENSG00000027075.14","gene_symbol":"PRKCH","gene_name":"protein kinase C eta [Source:HGNC Symbol;Acc:HGNC:9403]","synonyms":"PRKCL,PKCL,PKC-L","biotype":"protein_coding","ncbi_id":"5583","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. It is a calcium-independent and phospholipids-dependent protein kinase. It is predominantly expressed in epithelial tissues and has been shown to reside specifically in the cell nucleus. This protein kinase can regulate keratinocyte differentiation by activating the MAP kinase MAPK13 (p38delta)-activated protein kinase cascade that targets CCAAT/enhancer-binding protein alpha (CEBPA). It is also found to mediate the transcription activation of the transglutaminase 1 (TGM1) gene. Mutations in this gene are associated with susceptibility to cerebral infarction. [provided by RefSeq, Sep 2015]","start":61187559,"end":61550976,"strand":1,"description":"protein kinase C eta [Source:HGNC Symbol;Acc:HGNC:9403]"}, {"versioned_ensembl_gene_id":"ENSG00000080709.14","gene_symbol":"KCNN2","gene_name":"potassium calcium-activated channel subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:6291]","synonyms":"KCa2.2,hSK2","biotype":"protein_coding","ncbi_id":"3781","summary":"Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene is a member of the KCNN family of potassium channel genes. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":114360945,"end":114496500,"strand":1,"description":"potassium calcium-activated channel subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:6291]"}, {"versioned_ensembl_gene_id":"ENSG00000258684.2","gene_symbol":"BMS1P16","gene_name":"BMS1, ribosome biogenesis factor pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49161]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"727914","summary":null,"start":21160305,"end":21167357,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49161]"}, {"versioned_ensembl_gene_id":"ENSG00000250266.1","gene_symbol":"LINC01612","gene_name":"long intergenic non-protein coding RNA 1612 [Source:HGNC Symbol;Acc:HGNC:51837]","synonyms":"TCONS_00008319,RP11-789C1.1","biotype":"lincRNA","ncbi_id":"101928223","summary":null,"start":170273919,"end":170283079,"strand":1,"description":"long intergenic non-protein coding RNA 1612 [Source:HGNC Symbol;Acc:HGNC:51837]"}, {"versioned_ensembl_gene_id":"ENSG00000259295.6","gene_symbol":"CSPG4P12","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48362]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728121","summary":null,"start":85191438,"end":85213905,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48362]"}, {"versioned_ensembl_gene_id":"ENSG00000110871.14","gene_symbol":"COQ5","gene_name":"coenzyme Q5, methyltransferase [Source:HGNC Symbol;Acc:HGNC:28722]","synonyms":"MGC4767","biotype":"protein_coding","ncbi_id":"84274","summary":null,"start":120503274,"end":120534434,"strand":-1,"description":"coenzyme Q5, methyltransferase [Source:HGNC Symbol;Acc:HGNC:28722]"}, {"versioned_ensembl_gene_id":"ENSG00000243620.1","gene_symbol":"AC092957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146909685,"end":147370656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000040633.12","gene_symbol":"PHF23","gene_name":"PHD finger protein 23 [Source:HGNC Symbol;Acc:HGNC:28428]","synonyms":"MGC2941,FLJ16355","biotype":"protein_coding","ncbi_id":"79142","summary":null,"start":7235028,"end":7239722,"strand":-1,"description":"PHD finger protein 23 [Source:HGNC Symbol;Acc:HGNC:28428]"}, {"versioned_ensembl_gene_id":"ENSG00000276663.1","gene_symbol":"AC009090.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57245832,"end":57246396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267218.2","gene_symbol":"AC005336.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15902300,"end":15903238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156873.15","gene_symbol":"PHKG2","gene_name":"phosphorylase kinase catalytic subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:8931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5261","summary":"Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9C, also known as autosomal liver glycogenosis. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]","start":30748270,"end":30761176,"strand":1,"description":"phosphorylase kinase catalytic subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:8931]"}, {"versioned_ensembl_gene_id":"ENSG00000254249.1","gene_symbol":"AC100871.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124036010,"end":124040468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000025772.7","gene_symbol":"TOMM34","gene_name":"translocase of outer mitochondrial membrane 34 [Source:HGNC Symbol;Acc:HGNC:15746]","synonyms":"TOM34,HTOM34P","biotype":"protein_coding","ncbi_id":"10953","summary":"The protein encoded by this gene is involved in the import of precursor proteins into mitochondria. The encoded protein has a chaperone-like activity, binding the mature portion of unfolded proteins and aiding their import into mitochondria. This protein, which is found in the cytoplasm and sometimes associated with the outer mitochondrial membrane, has a weak ATPase activity and contains 6 TPR repeats. [provided by RefSeq, Jul 2008]","start":44942130,"end":44960486,"strand":-1,"description":"translocase of outer mitochondrial membrane 34 [Source:HGNC Symbol;Acc:HGNC:15746]"}, {"versioned_ensembl_gene_id":"ENSG00000266695.1","gene_symbol":"AC090958.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11911555,"end":11912686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236615.1","gene_symbol":"AC010086.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21405770,"end":21405995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275186.1","gene_symbol":"AC018445.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79470120,"end":79470940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279981.1","gene_symbol":"AC018445.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79496058,"end":79498348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279637.1","gene_symbol":"AC018445.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79420836,"end":79422780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262967.1","gene_symbol":"AC005921.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50693448,"end":50695449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203397.2","gene_symbol":"AL139400.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74066083,"end":74066592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218358.2","gene_symbol":"RAET1K","gene_name":"retinoic acid early transcript 1K pseudogene [Source:HGNC Symbol;Acc:HGNC:16797]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646024","summary":null,"start":149998019,"end":150005157,"strand":-1,"description":"retinoic acid early transcript 1K pseudogene [Source:HGNC Symbol;Acc:HGNC:16797]"}, {"versioned_ensembl_gene_id":"ENSG00000257258.1","gene_symbol":"AC012150.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29143196,"end":29148675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253189.1","gene_symbol":"AC079054.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6036433,"end":6036974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182707.4","gene_symbol":"FXYD6P3","gene_name":"FXYD domain containing ion transport regulator 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31124]","synonyms":"FXYD8","biotype":"processed_pseudogene","ncbi_id":"406875","summary":null,"start":73875068,"end":73875635,"strand":1,"description":"FXYD domain containing ion transport regulator 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31124]"}, {"versioned_ensembl_gene_id":"ENSG00000259203.1","gene_symbol":"AC016044.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52801614,"end":52804942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273069.1","gene_symbol":"AC211433.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74606913,"end":74607299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177108.5","gene_symbol":"ZDHHC22","gene_name":"zinc finger DHHC-type containing 22 [Source:HGNC Symbol;Acc:HGNC:20106]","synonyms":"C14orf59","biotype":"protein_coding","ncbi_id":"283576","summary":null,"start":77131270,"end":77142734,"strand":-1,"description":"zinc finger DHHC-type containing 22 [Source:HGNC Symbol;Acc:HGNC:20106]"}, {"versioned_ensembl_gene_id":"ENSG00000132570.14","gene_symbol":"PCBD2","gene_name":"pterin-4 alpha-carbinolamine dehydratase 2 [Source:HGNC Symbol;Acc:HGNC:24474]","synonyms":"DCOHM,DCOH2","biotype":"protein_coding","ncbi_id":"84105","summary":null,"start":134904906,"end":135007959,"strand":1,"description":"pterin-4 alpha-carbinolamine dehydratase 2 [Source:HGNC Symbol;Acc:HGNC:24474]"}, {"versioned_ensembl_gene_id":"ENSG00000105928.13","gene_symbol":"DFNA5","gene_name":"DFNA5, deafness associated tumor suppressor [Source:HGNC Symbol;Acc:HGNC:2810]","synonyms":"ICERE-1","biotype":"protein_coding","ncbi_id":"1687","summary":"Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":24698353,"end":24758113,"strand":-1,"description":"DFNA5, deafness associated tumor suppressor [Source:HGNC Symbol;Acc:HGNC:2810]"}, {"versioned_ensembl_gene_id":"ENSG00000257830.1","gene_symbol":"AC021066.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52274647,"end":52279156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282737.1","gene_symbol":"LINC01044","gene_name":"long intergenic non-protein coding RNA 1044 [Source:HGNC Symbol;Acc:HGNC:49032]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266956","summary":null,"start":112306417,"end":112315069,"strand":-1,"description":"long intergenic non-protein coding RNA 1044 [Source:HGNC Symbol;Acc:HGNC:49032]"}, {"versioned_ensembl_gene_id":"ENSG00000226541.1","gene_symbol":"AL359633.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46438310,"end":46438619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124126.13","gene_symbol":"PREX1","gene_name":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:32594]","synonyms":"P-REX1,KIAA1415","biotype":"protein_coding","ncbi_id":"57580","summary":"The protein encoded by this gene acts as a guanine nucleotide exchange factor for the RHO family of small GTP-binding proteins (RACs). It has been shown to bind to and activate RAC1 by exchanging bound GDP for free GTP. The encoded protein, which is found mainly in the cytoplasm, is activated by phosphatidylinositol-3,4,5-trisphosphate and the beta-gamma subunits of heterotrimeric G proteins. [provided by RefSeq, Jul 2008]","start":48624252,"end":48827883,"strand":-1,"description":"phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:32594]"}, {"versioned_ensembl_gene_id":"ENSG00000231251.1","gene_symbol":"AL021921.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30226523,"end":30226615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281103.1","gene_symbol":"TRG-AS1","gene_name":"T-cell receptor gamma locus antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48974]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506776","summary":null,"start":38341577,"end":38378804,"strand":1,"description":"T-cell receptor gamma locus antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48974]"}, {"versioned_ensembl_gene_id":"ENSG00000184983.9","gene_symbol":"NDUFA6","gene_name":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]","synonyms":"B14,NADHB14,LYRM6,CI-B14","biotype":"protein_coding","ncbi_id":"4700","summary":"This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016]","start":42085525,"end":42090955,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]"}, {"versioned_ensembl_gene_id":"ENSG00000270083.1","gene_symbol":"AL021878.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42089630,"end":42090028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258799.1","gene_symbol":"ZNF519P2","gene_name":"zinc finger protein 519 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50786]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287908","summary":null,"start":20901441,"end":20901609,"strand":-1,"description":"zinc finger protein 519 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50786]"}, {"versioned_ensembl_gene_id":"ENSG00000269931.1","gene_symbol":"AL078623.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12934877,"end":12935783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261554.1","gene_symbol":"AC037471.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20893383,"end":20893980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148384.12","gene_symbol":"INPP5E","gene_name":"inositol polyphosphate-5-phosphatase E [Source:HGNC Symbol;Acc:HGNC:21474]","synonyms":"PPI5PIV,pharbin,JBTS1,CORS1","biotype":"protein_coding","ncbi_id":"56623","summary":"The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. Studies of the mouse counterpart suggest that this protein may hydrolyze phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,5-bisphosphate on the cytoplasmic Golgi membrane and thereby regulate Golgi-vesicular trafficking. Mutations in this gene cause Joubert syndrome; a clinically and genetically heterogenous group of disorders characterized by midbrain-hindbrain malformation and various associated ciliopathies that include retinal dystrophy, nephronophthisis, liver fibrosis and polydactyly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":136428619,"end":136439823,"strand":-1,"description":"inositol polyphosphate-5-phosphatase E [Source:HGNC Symbol;Acc:HGNC:21474]"}, {"versioned_ensembl_gene_id":"ENSG00000156050.8","gene_symbol":"FAM161B","gene_name":"family with sequence similarity 161 member B [Source:HGNC Symbol;Acc:HGNC:19854]","synonyms":"C14orf44,FLJ31697","biotype":"protein_coding","ncbi_id":"145483","summary":null,"start":73931501,"end":73950414,"strand":-1,"description":"family with sequence similarity 161 member B [Source:HGNC Symbol;Acc:HGNC:19854]"}, {"versioned_ensembl_gene_id":"ENSG00000204460.3","gene_symbol":"LINC01854","gene_name":"long intergenic non-protein coding RNA 1854 [Source:HGNC Symbol;Acc:HGNC:52670]","synonyms":null,"biotype":"lincRNA","ncbi_id":"151121","summary":null,"start":129242173,"end":129273848,"strand":-1,"description":"long intergenic non-protein coding RNA 1854 [Source:HGNC Symbol;Acc:HGNC:52670]"}, {"versioned_ensembl_gene_id":"ENSG00000234814.8","gene_symbol":"SVILP1","gene_name":"supervillin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44959]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645954","summary":null,"start":30655489,"end":30717266,"strand":1,"description":"supervillin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44959]"}, {"versioned_ensembl_gene_id":"ENSG00000278627.1","gene_symbol":"AC005962.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58202352,"end":58203003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268055.1","gene_symbol":"AC067969.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38535517,"end":38537128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128242.12","gene_symbol":"GAL3ST1","gene_name":"galactose-3-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:24240]","synonyms":"CST","biotype":"protein_coding","ncbi_id":"9514","summary":"Sulfonation, an important step in the metabolism of many drugs, xenobiotics, hormones, and neurotransmitters, is catalyzed by sulfotransferases. This gene encodes galactosylceramide sulfotransferase, which catalyzes the sulfation of membrane glycolipids including the final step in the synthesis of sulfatide, a major lipid component of the myelin sheath. This gene exhibits elevated expression in ovarian epithelial carcinoma and the encoded enzyme exhibits elevated activity in renal cell carcinoma. Mutations in this gene may be associated with reduced insulin resistance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":30554635,"end":30574587,"strand":-1,"description":"galactose-3-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:24240]"}, {"versioned_ensembl_gene_id":"ENSG00000230031.10","gene_symbol":"POTEB2","gene_name":"POTE ankyrin domain family member B2 [Source:HGNC Symbol;Acc:HGNC:48327]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287399","summary":null,"start":20835372,"end":20866314,"strand":-1,"description":"POTE ankyrin domain family member B2 [Source:HGNC Symbol;Acc:HGNC:48327]"}, {"versioned_ensembl_gene_id":"ENSG00000114933.15","gene_symbol":"INO80D","gene_name":"INO80 complex subunit D [Source:HGNC Symbol;Acc:HGNC:25997]","synonyms":"FLJ20309","biotype":"protein_coding","ncbi_id":"54891","summary":null,"start":205993721,"end":206086303,"strand":-1,"description":"INO80 complex subunit D [Source:HGNC Symbol;Acc:HGNC:25997]"}, {"versioned_ensembl_gene_id":"ENSG00000272670.3","gene_symbol":"DOC2B","gene_name":"double C2 domain beta [Source:HGNC Symbol;Acc:HGNC:2986]","synonyms":"DOC2BL","biotype":"protein_coding","ncbi_id":"8447","summary":"There are at least two protein isoforms of the Double C2 protein, namely alpha (DOC2A) and beta (DOC2B), which contain two C2-like domains. DOC2A and DOC2B are encoded by different genes; these genes are at times confused with the unrelated DAB2 gene which was initially named DOC-2. DOC2B is expressed ubiquitously and is suggested to be involved in Ca(2+)-dependent intracellular vesicle trafficking in various types of cells. [provided by RefSeq, Jul 2008]","start":142789,"end":180568,"strand":-1,"description":"double C2 domain beta [Source:HGNC Symbol;Acc:HGNC:2986]"}, {"versioned_ensembl_gene_id":"ENSG00000126561.16","gene_symbol":"STAT5A","gene_name":"signal transducer and activator of transcription 5A [Source:HGNC Symbol;Acc:HGNC:11366]","synonyms":"STAT5,MGF","biotype":"protein_coding","ncbi_id":"6776","summary":"The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated by, and mediates the responses of many cell ligands, such as IL2, IL3, IL7 GM-CSF, erythropoietin, thrombopoietin, and different growth hormones. Activation of this protein in myeloma and lymphoma associated with a TEL/JAK2 gene fusion is independent of cell stimulus and has been shown to be essential for tumorigenesis. The mouse counterpart of this gene is found to induce the expression of BCL2L1/BCL-X(L), which suggests the antiapoptotic function of this gene in cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":42287547,"end":42311943,"strand":1,"description":"signal transducer and activator of transcription 5A [Source:HGNC Symbol;Acc:HGNC:11366]"}, {"versioned_ensembl_gene_id":"ENSG00000229551.2","gene_symbol":"GAPDHP17","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37765]","synonyms":"GAPDHP18","biotype":"processed_pseudogene","ncbi_id":"360008","summary":null,"start":20861337,"end":20862337,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37765]"}, {"versioned_ensembl_gene_id":"ENSG00000172404.4","gene_symbol":"DNAJB7","gene_name":"DnaJ heat shock protein family (Hsp40) member B7 [Source:HGNC Symbol;Acc:HGNC:24986]","synonyms":"HSC3","biotype":"protein_coding","ncbi_id":"150353","summary":"The protein encoded by this intronless gene belongs to the evolutionarily conserved DNAJ/HSP40 family of proteins, which regulate molecular chaperone activity by stimulating ATPase activity. DNAJ proteins may have up to 3 distinct domains: a conserved 70-amino acid J domain, usually at the N terminus; a glycine/phenylalanine (G/F)-rich region; and a cysteine-rich domain containing 4 motifs resembling a zinc finger domain.[provided by RefSeq, Mar 2011]","start":40859549,"end":40862126,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B7 [Source:HGNC Symbol;Acc:HGNC:24986]"}, {"versioned_ensembl_gene_id":"ENSG00000096063.15","gene_symbol":"SRPK1","gene_name":"SRSF protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:11305]","synonyms":"SFRSK1","biotype":"protein_coding","ncbi_id":"6732","summary":"This gene encodes a serine/arginine protein kinase specific for the SR (serine/arginine-rich domain) family of splicing factors. The protein localizes to the nucleus and the cytoplasm. It is thought to play a role in regulation of both constitutive and alternative splicing by regulating intracellular localization of splicing factors. Alternative splicing of this gene results in multiple transcript variants. Additional alternatively spliced transcript variants have been described for this gene, but their full length nature have not been determined.[provided by RefSeq, Jul 2010]","start":35832966,"end":35921342,"strand":-1,"description":"SRSF protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:11305]"}, {"versioned_ensembl_gene_id":"ENSG00000229079.1","gene_symbol":"CR848007.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42959280,"end":42960066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185664.14","gene_symbol":"PMEL","gene_name":"premelanosome protein [Source:HGNC Symbol;Acc:HGNC:10880]","synonyms":"SILV,SIL,SI,Pmel17,gp100,D12S53E","biotype":"protein_coding","ncbi_id":"6490","summary":"This gene encodes a melanocyte-specific type I transmembrane glycoprotein. The encoded protein is enriched in melanosomes, which are the melanin-producing organelles in melanocytes, and plays an essential role in the structural organization of premelanosomes. This protein is involved in generating internal matrix fibers that define the transition from Stage I to Stage II melanosomes. This protein undergoes a complex pattern of prosttranslational processing and modification that is essential to the proper functioning of the protein. A secreted form of this protein that is released by proteolytic ectodomain shedding may be used as a melanoma-specific serum marker. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]","start":55954105,"end":55973317,"strand":-1,"description":"premelanosome protein [Source:HGNC Symbol;Acc:HGNC:10880]"}, {"versioned_ensembl_gene_id":"ENSG00000181904.8","gene_symbol":"C5orf24","gene_name":"chromosome 5 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:26746]","synonyms":"FLJ37562","biotype":"protein_coding","ncbi_id":"134553","summary":null,"start":134845680,"end":134859737,"strand":1,"description":"chromosome 5 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:26746]"}, {"versioned_ensembl_gene_id":"ENSG00000233876.2","gene_symbol":"GAPDHP68","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:4146]","synonyms":"GAPDL13,GAPDHL13","biotype":"processed_pseudogene","ncbi_id":"100132601","summary":null,"start":9614978,"end":9615985,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:4146]"}, {"versioned_ensembl_gene_id":"ENSG00000281460.1","gene_symbol":"AL049541.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48476999,"end":48477553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092098.16","gene_symbol":"RNF31","gene_name":"ring finger protein 31 [Source:HGNC Symbol;Acc:HGNC:16031]","synonyms":"ZIBRA,Paul,HOIP,FLJ23501,FLJ10111","biotype":"protein_coding","ncbi_id":"55072","summary":"The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The encoded protein is the E3 ubiquitin-protein ligase component of the linear ubiquitin chain assembly complex. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":24146683,"end":24160661,"strand":1,"description":"ring finger protein 31 [Source:HGNC Symbol;Acc:HGNC:16031]"}, {"versioned_ensembl_gene_id":"ENSG00000214691.7","gene_symbol":"LINC01913","gene_name":"long intergenic non-protein coding RNA 1913 [Source:HGNC Symbol;Acc:HGNC:52732]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388942","summary":null,"start":41877074,"end":41894046,"strand":1,"description":"long intergenic non-protein coding RNA 1913 [Source:HGNC Symbol;Acc:HGNC:52732]"}, {"versioned_ensembl_gene_id":"ENSG00000181610.12","gene_symbol":"MRPS23","gene_name":"mitochondrial ribosomal protein S23 [Source:HGNC Symbol;Acc:HGNC:14509]","synonyms":"MRP-S23,HSPC329,CGI-138","biotype":"protein_coding","ncbi_id":"51649","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. A pseudogene corresponding to this gene is found on chromosome 7p. [provided by RefSeq, Jul 2008]","start":57834781,"end":57850056,"strand":-1,"description":"mitochondrial ribosomal protein S23 [Source:HGNC Symbol;Acc:HGNC:14509]"}, {"versioned_ensembl_gene_id":"ENSG00000269848.1","gene_symbol":"AC119751.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49524030,"end":49524185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133962.7","gene_symbol":"CATSPERB","gene_name":"cation channel sperm associated auxiliary subunit beta [Source:HGNC Symbol;Acc:HGNC:20500]","synonyms":"FLJ14298,C14orf161","biotype":"protein_coding","ncbi_id":"79820","summary":null,"start":91580696,"end":91780707,"strand":-1,"description":"cation channel sperm associated auxiliary subunit beta [Source:HGNC Symbol;Acc:HGNC:20500]"}, {"versioned_ensembl_gene_id":"ENSG00000279628.1","gene_symbol":"AC131280.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20658900,"end":20664970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134375.10","gene_symbol":"TIMM17A","gene_name":"translocase of inner mitochondrial membrane 17A [Source:HGNC Symbol;Acc:HGNC:17315]","synonyms":"TIM17A,TIM17","biotype":"protein_coding","ncbi_id":"10440","summary":null,"start":201955491,"end":201970661,"strand":1,"description":"translocase of inner mitochondrial membrane 17A [Source:HGNC Symbol;Acc:HGNC:17315]"}, {"versioned_ensembl_gene_id":"ENSG00000258388.7","gene_symbol":"PPT2-EGFL8","gene_name":"PPT2-EGFL8 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48343]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532746","summary":"This locus represents naturally occurring read-through transcription between the neighboring PPT2 (palmitoyl-protein thioesterase 2) and EGFL8 (EGF-like-domain, multiple 8) genes located in the major histocompatibility complex class III region of chromosome 6. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":32153845,"end":32171978,"strand":1,"description":"PPT2-EGFL8 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48343]"}, {"versioned_ensembl_gene_id":"ENSG00000236748.1","gene_symbol":"AC009500.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8938787,"end":8939369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260647.1","gene_symbol":"AC127537.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18268080,"end":18268828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109576.13","gene_symbol":"AADAT","gene_name":"aminoadipate aminotransferase [Source:HGNC Symbol;Acc:HGNC:17929]","synonyms":"KYAT2,KATII,KAT2","biotype":"protein_coding","ncbi_id":"51166","summary":"This gene encodes a protein that is highly similar to mouse and rat kynurenine aminotransferase II. The rat protein is a homodimer with two transaminase activities. One activity is the transamination of alpha-aminoadipic acid, a final step in the saccaropine pathway which is the major pathway for L-lysine catabolism. The other activity involves the transamination of kynurenine to produce kynurenine acid, the precursor of kynurenic acid which has neuroprotective properties. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":170060222,"end":170091699,"strand":-1,"description":"aminoadipate aminotransferase [Source:HGNC Symbol;Acc:HGNC:17929]"}, {"versioned_ensembl_gene_id":"ENSG00000224758.1","gene_symbol":"LINC01167","gene_name":"long intergenic non-protein coding RNA 1167 [Source:HGNC Symbol;Acc:HGNC:49536]","synonyms":"TCONS_00018075","biotype":"lincRNA","ncbi_id":"103695432","summary":null,"start":132961340,"end":132962237,"strand":-1,"description":"long intergenic non-protein coding RNA 1167 [Source:HGNC Symbol;Acc:HGNC:49536]"}, {"versioned_ensembl_gene_id":"ENSG00000135002.11","gene_symbol":"RFK","gene_name":"riboflavin kinase [Source:HGNC Symbol;Acc:HGNC:30324]","synonyms":"RIFK,FLJ11149","biotype":"protein_coding","ncbi_id":"55312","summary":"Riboflavin kinase (RFK; EC 2.7.1.26) is an essential enzyme that catalyzes the phosphorylation of riboflavin (vitamin B2) to form flavin mononucleotide (FMN), an obligatory step in vitamin B2 utilization and flavin cofactor synthesis (Karthikeyan et al., 2003 [PubMed 12623014]).[supplied by OMIM, Nov 2009]","start":76385517,"end":76394517,"strand":-1,"description":"riboflavin kinase [Source:HGNC Symbol;Acc:HGNC:30324]"}, {"versioned_ensembl_gene_id":"ENSG00000122584.12","gene_symbol":"NXPH1","gene_name":"neurexophilin 1 [Source:HGNC Symbol;Acc:HGNC:20693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30010","summary":"This gene is a member of the neurexophilin family and encodes a secreted protein with a variable N-terminal domain, a highly conserved, N-glycosylated central domain, a short linker region, and a cysteine-rich C-terminal domain. This protein forms a very tight complex with alpha neurexins, a group of proteins that promote adhesion between dendrites and axons. [provided by RefSeq, Jul 2008]","start":8433955,"end":8752963,"strand":1,"description":"neurexophilin 1 [Source:HGNC Symbol;Acc:HGNC:20693]"}, {"versioned_ensembl_gene_id":"ENSG00000198692.9","gene_symbol":"EIF1AY","gene_name":"eukaryotic translation initiation factor 1A, Y-linked [Source:HGNC Symbol;Acc:HGNC:3252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9086","summary":"This gene is located on the non-recombining region of the Y chromosome. It encodes a protein related to eukaryotic translation initiation factor 1A (EIF1A), which may function in stabilizing the binding of the initiator Met-tRNA to 40S ribosomal subunits. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":20575725,"end":20593154,"strand":1,"description":"eukaryotic translation initiation factor 1A, Y-linked [Source:HGNC Symbol;Acc:HGNC:3252]"}, {"versioned_ensembl_gene_id":"ENSG00000234735.1","gene_symbol":"AL022237.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43092167,"end":43092524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099194.5","gene_symbol":"SCD","gene_name":"stearoyl-CoA desaturase [Source:HGNC Symbol;Acc:HGNC:10571]","synonyms":"SCDOS,FADS5","biotype":"protein_coding","ncbi_id":"6319","summary":"This gene encodes an enzyme involved in fatty acid biosynthesis, primarily the synthesis of oleic acid. The protein belongs to the fatty acid desaturase family and is an integral membrane protein located in the endoplasmic reticulum. Transcripts of approximately 3.9 and 5.2 kb, differing only by alternative polyadenlyation signals, have been detected. A gene encoding a similar enzyme is located on chromosome 4 and a pseudogene of this gene is located on chromosome 17. [provided by RefSeq, Sep 2015]","start":100347124,"end":100364834,"strand":1,"description":"stearoyl-CoA desaturase [Source:HGNC Symbol;Acc:HGNC:10571]"}, {"versioned_ensembl_gene_id":"ENSG00000257472.1","gene_symbol":"AL355112.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31925801,"end":31930146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250929.2","gene_symbol":"LINC01181","gene_name":"long intergenic non-protein coding RNA 1181 [Source:HGNC Symbol;Acc:HGNC:25533]","synonyms":"FLJ10489","biotype":"antisense_RNA","ncbi_id":"379034","summary":null,"start":103121032,"end":103132966,"strand":1,"description":"long intergenic non-protein coding RNA 1181 [Source:HGNC Symbol;Acc:HGNC:25533]"}, {"versioned_ensembl_gene_id":"ENSG00000108688.11","gene_symbol":"CCL7","gene_name":"C-C motif chemokine ligand 7 [Source:HGNC Symbol;Acc:HGNC:10634]","synonyms":"MCP-3,MARC,FIC,SCYA7,SCYA6,NC28,MCP3","biotype":"protein_coding","ncbi_id":"6354","summary":"This gene encodes monocyte chemotactic protein 3, a secreted chemokine which attracts macrophages during inflammation and metastasis. It is a member of the C-C subfamily of chemokines which are characterized by having two adjacent cysteine residues. The protein is an in vivo substrate of matrix metalloproteinase 2, an enzyme which degrades components of the extracellular matrix. This gene is part of a cluster of C-C chemokine family members on chromosome 17q. [provided by RefSeq, Jul 2008]","start":34270221,"end":34272242,"strand":1,"description":"C-C motif chemokine ligand 7 [Source:HGNC Symbol;Acc:HGNC:10634]"}, {"versioned_ensembl_gene_id":"ENSG00000126062.3","gene_symbol":"TMEM115","gene_name":"transmembrane protein 115 [Source:HGNC Symbol;Acc:HGNC:30055]","synonyms":"PL6","biotype":"protein_coding","ncbi_id":"11070","summary":null,"start":50354749,"end":50359610,"strand":-1,"description":"transmembrane protein 115 [Source:HGNC Symbol;Acc:HGNC:30055]"}, {"versioned_ensembl_gene_id":"ENSG00000204118.2","gene_symbol":"NAP1L6","gene_name":"nucleosome assembly protein 1 like 6 [Source:HGNC Symbol;Acc:HGNC:31706]","synonyms":"FLJ33596","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645996","summary":null,"start":73126037,"end":73128080,"strand":-1,"description":"nucleosome assembly protein 1 like 6 [Source:HGNC Symbol;Acc:HGNC:31706]"}, {"versioned_ensembl_gene_id":"ENSG00000228422.3","gene_symbol":"LINC00687","gene_name":"long intergenic non-protein coding RNA 687 [Source:HGNC Symbol;Acc:HGNC:16194]","synonyms":"dJ1012F16.1,C20orf61","biotype":"lincRNA","ncbi_id":"728450","summary":null,"start":11800463,"end":11870715,"strand":-1,"description":"long intergenic non-protein coding RNA 687 [Source:HGNC Symbol;Acc:HGNC:16194]"}, {"versioned_ensembl_gene_id":"ENSG00000272104.1","gene_symbol":"Z84492.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50350892,"end":50367923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223826.1","gene_symbol":"LINC01870","gene_name":"long intergenic non-protein coding RNA 1870 [Source:HGNC Symbol;Acc:HGNC:52689]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985925","summary":null,"start":101479390,"end":101486822,"strand":1,"description":"long intergenic non-protein coding RNA 1870 [Source:HGNC Symbol;Acc:HGNC:52689]"}, {"versioned_ensembl_gene_id":"ENSG00000224245.1","gene_symbol":"AL358232.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94496275,"end":94512879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183023.18","gene_symbol":"SLC8A1","gene_name":"solute carrier family 8 member A1 [Source:HGNC Symbol;Acc:HGNC:11068]","synonyms":"NCX1","biotype":"protein_coding","ncbi_id":"6546","summary":"In cardiac myocytes, Ca(2+) concentrations alternate between high levels during contraction and low levels during relaxation. The increase in Ca(2+) concentration during contraction is primarily due to release of Ca(2+) from intracellular stores. However, some Ca(2+) also enters the cell through the sarcolemma (plasma membrane). During relaxation, Ca(2+) is sequestered within the intracellular stores. To prevent overloading of intracellular stores, the Ca(2+) that entered across the sarcolemma must be extruded from the cell. The Na(+)-Ca(2+) exchanger is the primary mechanism by which the Ca(2+) is extruded from the cell during relaxation. In the heart, the exchanger may play a key role in digitalis action. The exchanger is the dominant mechanism in returning the cardiac myocyte to its resting state following excitation.[supplied by OMIM, Apr 2004]","start":40097270,"end":40611053,"strand":-1,"description":"solute carrier family 8 member A1 [Source:HGNC Symbol;Acc:HGNC:11068]"}, {"versioned_ensembl_gene_id":"ENSG00000116127.17","gene_symbol":"ALMS1","gene_name":"ALMS1, centrosome and basal body associated protein [Source:HGNC Symbol;Acc:HGNC:428]","synonyms":"KIAA0328","biotype":"protein_coding","ncbi_id":"7840","summary":"This gene encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations in this gene cause Alstrom syndrome. There is a pseudogene for this gene located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. [provided by RefSeq, Apr 2014]","start":73385758,"end":73610793,"strand":1,"description":"ALMS1, centrosome and basal body associated protein [Source:HGNC Symbol;Acc:HGNC:428]"}, {"versioned_ensembl_gene_id":"ENSG00000230778.1","gene_symbol":"ANKRD63","gene_name":"ankyrin repeat domain 63 [Source:HGNC Symbol;Acc:HGNC:40027]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131244","summary":null,"start":40281444,"end":40282586,"strand":-1,"description":"ankyrin repeat domain 63 [Source:HGNC Symbol;Acc:HGNC:40027]"}, {"versioned_ensembl_gene_id":"ENSG00000250705.1","gene_symbol":"AC008526.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88602780,"end":88603117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274392.3","gene_symbol":"AC093724.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131722418,"end":131768326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119661.14","gene_symbol":"DNAL1","gene_name":"dynein axonemal light chain 1 [Source:HGNC Symbol;Acc:HGNC:23247]","synonyms":"MGC12435,CILD16,C14orf168,1700010H15RiK","biotype":"protein_coding","ncbi_id":"83544","summary":"This gene encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]","start":73644875,"end":73703732,"strand":1,"description":"dynein axonemal light chain 1 [Source:HGNC Symbol;Acc:HGNC:23247]"}, {"versioned_ensembl_gene_id":"ENSG00000206452.10","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31258588,"end":31261959,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000250315.2","gene_symbol":"AC110760.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":75101477,"end":75101943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249487.6","gene_symbol":"LINC01586","gene_name":"long intergenic non-protein coding RNA 1586 [Source:HGNC Symbol;Acc:HGNC:51434]","synonyms":"TCONS_00023252","biotype":"lincRNA","ncbi_id":"101929743","summary":null,"start":88585566,"end":88605110,"strand":-1,"description":"long intergenic non-protein coding RNA 1586 [Source:HGNC Symbol;Acc:HGNC:51434]"}, {"versioned_ensembl_gene_id":"ENSG00000253481.2","gene_symbol":"IGKV1OR22-1","gene_name":"immunoglobulin kappa variable 1/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5772]","synonyms":"IGKVP5,IGKV1/OR22-1","biotype":"IG_V_pseudogene","ncbi_id":"3530","summary":null,"start":16933521,"end":16934003,"strand":-1,"description":"immunoglobulin kappa variable 1/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5772]"}, {"versioned_ensembl_gene_id":"ENSG00000130950.13","gene_symbol":"NUTM2F","gene_name":"NUT family member 2F [Source:HGNC Symbol;Acc:HGNC:23450]","synonyms":"FAM22F,DKFZp434I1117","biotype":"protein_coding","ncbi_id":"54754","summary":null,"start":94318196,"end":94328644,"strand":-1,"description":"NUT family member 2F [Source:HGNC Symbol;Acc:HGNC:23450]"}, {"versioned_ensembl_gene_id":"ENSG00000000003.14","gene_symbol":"TSPAN6","gene_name":"tetraspanin 6 [Source:HGNC Symbol;Acc:HGNC:11858]","synonyms":"TSPAN-6,TM4SF6,T245","biotype":"protein_coding","ncbi_id":"7105","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. The protein encoded by this gene is a cell surface glycoprotein and is highly similar in sequence to the transmembrane 4 superfamily member 2 protein. It functions as a negative regulator of retinoic acid-inducible gene I-like receptor-mediated immune signaling via its interaction with the mitochondrial antiviral signaling-centered signalosome. This gene uses alternative polyadenylation sites, and multiple transcript variants result from alternative splicing. [provided by RefSeq, Jul 2013]","start":100627109,"end":100639991,"strand":-1,"description":"tetraspanin 6 [Source:HGNC Symbol;Acc:HGNC:11858]"}, {"versioned_ensembl_gene_id":"ENSG00000137709.9","gene_symbol":"POU2F3","gene_name":"POU class 2 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:19864]","synonyms":"Skn-1a,PLA-1,OCT11,Epoc-1","biotype":"protein_coding","ncbi_id":"25833","summary":"This gene encodes a member of the POU domain family of transcription factors. POU domain transcription factors bind to a specific octamer DNA motif and regulate cell type-specific differentiation pathways. The encoded protein is primarily expressed in the epidermis, and plays a critical role in keratinocyte proliferation and differentiation. The encoded protein is also a candidate tumor suppressor protein, and aberrant promoter methylation of this gene may play a role in cervical cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":120236640,"end":120319944,"strand":1,"description":"POU class 2 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:19864]"}, {"versioned_ensembl_gene_id":"ENSG00000160404.17","gene_symbol":"TOR2A","gene_name":"torsin family 2 member A [Source:HGNC Symbol;Acc:HGNC:11996]","synonyms":"FLJ14771,TORP1","biotype":"protein_coding","ncbi_id":"27433","summary":"This gene encodes a member of the AAA family of adenosine triphosphatases with similarity to Clp proteases and heat shock proteins. Alternative splicing at this locus results in the translation of multiple isoforms of the encoded protein, some of which contain salusin peptides in the C-terminal region. These peptides may play roles in hypotension, myocardial growth and the induction of mitogenesis, and may also be involved in the pathogenesis of atherosclerosis. The antimicrobial peptide salusin-beta has antibacterial activity. [provided by RefSeq, Nov 2014]","start":127731524,"end":127735317,"strand":-1,"description":"torsin family 2 member A [Source:HGNC Symbol;Acc:HGNC:11996]"}, {"versioned_ensembl_gene_id":"ENSG00000270994.1","gene_symbol":"AL157899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183709305,"end":183710240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000094755.16","gene_symbol":"GABRP","gene_name":"gamma-aminobutyric acid type A receptor pi subunit [Source:HGNC Symbol;Acc:HGNC:4089]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2568","summary":"The gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. The subunit encoded by this gene is expressed in several non-neuronal tissues including the uterus and ovaries. This subunit can assemble with known GABA A receptor subunits, and the presence of this subunit alters the sensitivity of recombinant receptors to modulatory agents such as pregnanolone. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":170763350,"end":170814047,"strand":1,"description":"gamma-aminobutyric acid type A receptor pi subunit [Source:HGNC Symbol;Acc:HGNC:4089]"}, {"versioned_ensembl_gene_id":"ENSG00000227554.1","gene_symbol":"AL590422.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":183754418,"end":183754937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253348.1","gene_symbol":"AC008514.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170747047,"end":170788650,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167981.5","gene_symbol":"ZNF597","gene_name":"zinc finger protein 597 [Source:HGNC Symbol;Acc:HGNC:26573]","synonyms":"HIT-4,FLJ33071","biotype":"protein_coding","ncbi_id":"146434","summary":"This gene encodes a protein with multiple zinc finger domains. Loss of the related gene in rodents results in defects in neural development and embryonic lethality in mutant homozygotes. This gene is adjacent to a differentially methylated region (DMR) and is imprinted and maternally expressed. [provided by RefSeq, Nov 2015]","start":3432422,"end":3443542,"strand":-1,"description":"zinc finger protein 597 [Source:HGNC Symbol;Acc:HGNC:26573]"}, {"versioned_ensembl_gene_id":"ENSG00000259569.2","gene_symbol":"AC013489.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88568287,"end":88568562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143344.15","gene_symbol":"RGL1","gene_name":"ral guanine nucleotide dissociation stimulator like 1 [Source:HGNC Symbol;Acc:HGNC:30281]","synonyms":"RGL","biotype":"protein_coding","ncbi_id":"23179","summary":null,"start":183636085,"end":183928531,"strand":1,"description":"ral guanine nucleotide dissociation stimulator like 1 [Source:HGNC Symbol;Acc:HGNC:30281]"}, {"versioned_ensembl_gene_id":"ENSG00000100271.16","gene_symbol":"TTLL1","gene_name":"tubulin tyrosine ligase like 1 [Source:HGNC Symbol;Acc:HGNC:1312]","synonyms":"C22orf7","biotype":"protein_coding","ncbi_id":"25809","summary":null,"start":43039644,"end":43089428,"strand":-1,"description":"tubulin tyrosine ligase like 1 [Source:HGNC Symbol;Acc:HGNC:1312]"}, {"versioned_ensembl_gene_id":"ENSG00000175356.12","gene_symbol":"SCUBE2","gene_name":"signal peptide, CUB domain and EGF like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30425]","synonyms":"FLJ16792,Cegf1,Cegb1","biotype":"protein_coding","ncbi_id":"57758","summary":null,"start":9020391,"end":9138114,"strand":-1,"description":"signal peptide, CUB domain and EGF like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30425]"}, {"versioned_ensembl_gene_id":"ENSG00000178473.6","gene_symbol":"UCN3","gene_name":"urocortin 3 [Source:HGNC Symbol;Acc:HGNC:17781]","synonyms":"UCNIII,SPC","biotype":"protein_coding","ncbi_id":"114131","summary":"This gene encodes a member of the sauvagine/corticotropin-releasing factor/urotensin I family of proteins. The encoded preproprotein is proteolytically processed to generate the mature peptide hormone, which is secreted by pancreatic beta and alpha cells. This hormone is an endogenous ligand for corticotropin-releasing factor receptor 2 and may regulate insulin secretion in response to plasma glucose levels. Patients with type 2 diabetes exhibit reduced levels of the encoded protein in beta cells. In the brain, the encoded protein may be responsible for the effects of stress on appetite. [provided by RefSeq, May 2016]","start":5365009,"end":5374692,"strand":1,"description":"urocortin 3 [Source:HGNC Symbol;Acc:HGNC:17781]"}, {"versioned_ensembl_gene_id":"ENSG00000281590.1","gene_symbol":"AC107911.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1187118,"end":1190311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256262.1","gene_symbol":"USP30-AS1","gene_name":"USP30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40909]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131733","summary":null,"start":109052350,"end":109053952,"strand":-1,"description":"USP30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40909]"}, {"versioned_ensembl_gene_id":"ENSG00000282604.1","gene_symbol":"CCL4L2","gene_name":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9560","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this family member is similar to the chemokine (C-C motif) ligand 4 product, which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals, where most individuals have one to five copies. This gene copy contains a non-consensus splice acceptor site at the 3' terminal exon found in other highly similar gene copies, and it thus uses other alternative splice sites for the 3' terminal exon, resulting in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36210948,"end":36212918,"strand":1,"description":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]"}, {"versioned_ensembl_gene_id":"ENSG00000109072.13","gene_symbol":"VTN","gene_name":"vitronectin [Source:HGNC Symbol;Acc:HGNC:12724]","synonyms":"VN","biotype":"protein_coding","ncbi_id":"7448","summary":"The protein encoded by this gene functions in part as an adhesive glycoprotein. Differential expression of this protein can promote either cell adhesion or migration as it links cells to the extracellular matrix through a variety of ligands. These ligands include integrins, plasminogen activator inhibitor-1, and urokinase plasminogen activator receptor. This secreted protein can be present in the plasma as a monomer or dimer and forms a multimer in the extracellular matrix of several tissues. This protein also inhibits the membrane-damaging effect of the terminal cytolytic complement pathway and binds to several serpin serine protease inhibitors. This protein can also promote extracellular matrix degradation and thus plays a role in tumorigenesis. It is involved in a variety of other biological processes such as the regulation of the coagulation pathway, wound healing, and tissue remodeling. The heparin-binding domain of this protein give it anti-microbial properties. It is also a lipid binding protein that forms a principal component of high density lipoprotein. [provided by RefSeq, Aug 2020]","start":28367276,"end":28373091,"strand":-1,"description":"vitronectin [Source:HGNC Symbol;Acc:HGNC:12724]"}, {"versioned_ensembl_gene_id":"ENSG00000244239.1","gene_symbol":"AC007009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8262233,"end":8262821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233061.1","gene_symbol":"TTLL7-IT1","gene_name":"TTLL7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41486]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874314","summary":null,"start":83979118,"end":83984300,"strand":-1,"description":"TTLL7 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41486]"}, {"versioned_ensembl_gene_id":"ENSG00000263571.2","gene_symbol":"AC004147.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34155566,"end":34165679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248834.2","gene_symbol":"MARK2P5","gene_name":"microtubule affinity regulating kinase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39796]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421485","summary":null,"start":15384220,"end":15384853,"strand":1,"description":"microtubule affinity regulating kinase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39796]"}, {"versioned_ensembl_gene_id":"ENSG00000114125.13","gene_symbol":"RNF7","gene_name":"ring finger protein 7 [Source:HGNC Symbol;Acc:HGNC:10070]","synonyms":"SAG,ROC2,CKBBP1","biotype":"protein_coding","ncbi_id":"9616","summary":"The protein encoded by this gene is a highly conserved ring finger protein. It is an essential subunit of SKP1-cullin/CDC53-F box protein ubiquitin ligases, which are a part of the protein degradation machinery important for cell cycle progression and signal transduction. This protein interacts with, and is a substrate of, casein kinase II (CSNK2A1/CKII). The phosphorylation of this protein by CSNK2A1 has been shown to promote the degradation of IkappaBalpha (CHUK/IKK-alpha/IKBKA) and p27Kip1(CDKN1B). Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":141738204,"end":141747560,"strand":1,"description":"ring finger protein 7 [Source:HGNC Symbol;Acc:HGNC:10070]"}, {"versioned_ensembl_gene_id":"ENSG00000134864.10","gene_symbol":"GGACT","gene_name":"gamma-glutamylamine cyclotransferase [Source:HGNC Symbol;Acc:HGNC:25100]","synonyms":"A2LD1","biotype":"protein_coding","ncbi_id":"87769","summary":"The protein encoded by this gene aids in the proteolytic degradation of crosslinked fibrin by breaking down isodipeptide L-gamma-glutamyl-L-epsilon-lysine, a byproduct of fibrin degradation. The reaction catalyzed by the encoded gamma-glutamylaminecyclotransferase produces 5-oxo-L-proline and a free alkylamine. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Aug 2010]","start":100530164,"end":100589528,"strand":-1,"description":"gamma-glutamylamine cyclotransferase [Source:HGNC Symbol;Acc:HGNC:25100]"}, {"versioned_ensembl_gene_id":"ENSG00000237016.1","gene_symbol":"AC013410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173575110,"end":173576341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283108.1","gene_symbol":"AC011451.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9383581,"end":9407055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282728.1","gene_symbol":"PGR-AS1","gene_name":"PGR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52650]","synonyms":"AT3,AT2,AT1","biotype":"processed_transcript","ncbi_id":"101054525","summary":null,"start":101129077,"end":101209591,"strand":1,"description":"PGR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52650]"}, {"versioned_ensembl_gene_id":"ENSG00000003436.15","gene_symbol":"TFPI","gene_name":"tissue factor pathway inhibitor [Source:HGNC Symbol;Acc:HGNC:11760]","synonyms":"TFPI1,TFI,LACI,EPI","biotype":"protein_coding","ncbi_id":"7035","summary":"This gene encodes a Kunitz-type serine protease inhibitor that regulates the tissue factor (TF)-dependent pathway of blood coagulation. The coagulation process initiates with the formation of a factor VIIa-TF complex, which proteolytically activates additional proteases (factors IX and X) and ultimately leads to the formation of a fibrin clot. The product of this gene inhibits the activated factor X and VIIa-TF proteases in an autoregulatory loop. Inhibition of the encoded protein restores hemostasis in animal models of hemophilia. This gene encodes multiple protein isoforms that differ in their inhibitory activity, specificity and cellular localization. [provided by RefSeq, Jul 2016]","start":187464230,"end":187565760,"strand":-1,"description":"tissue factor pathway inhibitor [Source:HGNC Symbol;Acc:HGNC:11760]"}, {"versioned_ensembl_gene_id":"ENSG00000232824.1","gene_symbol":"PRR13P1","gene_name":"proline rich 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647195","summary":null,"start":198197779,"end":198198186,"strand":-1,"description":"proline rich 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50614]"}, {"versioned_ensembl_gene_id":"ENSG00000163687.13","gene_symbol":"DNASE1L3","gene_name":"deoxyribonuclease 1 like 3 [Source:HGNC Symbol;Acc:HGNC:2959]","synonyms":"LSD,DNAS1L3","biotype":"protein_coding","ncbi_id":"1776","summary":"This gene encodes a member of the deoxyribonuclease I family. The encoded protein hydrolyzes DNA, is not inhibited by actin, and mediates the breakdown of DNA during apoptosis. Mutations in this gene are a cause of systemic lupus erythematosus-16. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":58192257,"end":58214697,"strand":-1,"description":"deoxyribonuclease 1 like 3 [Source:HGNC Symbol;Acc:HGNC:2959]"}, {"versioned_ensembl_gene_id":"ENSG00000277008.1","gene_symbol":"TEX28P2","gene_name":"testis expressed 28 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33357]","synonyms":"pTEX,CXorf2B","biotype":"unprocessed_pseudogene","ncbi_id":"653363","summary":null,"start":154159357,"end":154176349,"strand":-1,"description":"testis expressed 28 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33357]"}, {"versioned_ensembl_gene_id":"ENSG00000278741.4","gene_symbol":"ABR","gene_name":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]","synonyms":"MDB","biotype":"protein_coding","ncbi_id":"29","summary":"This gene encodes a protein that is similar to the protein encoded by the breakpoint cluster region gene located on chromosome 22. The protein encoded by this gene contains a GTPase-activating protein domain, a domain found in members of the Rho family of GTP-binding proteins. Functional studies in mice determined that this protein plays a role in vestibular morphogenesis. Alternatively spliced transcript variants have been reported for this gene. [provided by RefSeq, Feb 2012]","start":1003519,"end":1192547,"strand":-1,"description":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]"}, {"versioned_ensembl_gene_id":"ENSG00000261069.3","gene_symbol":"AC124312.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25087661,"end":25088896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112473.17","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"D6S2244E,ZIP7,HKE4,RING5,H2-KE4,KE4","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33200445,"end":33204439,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000281251.1","gene_symbol":"AC107911.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1160565,"end":1160774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256789.1","gene_symbol":"AP000753.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63637677,"end":63658962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237167.1","gene_symbol":"AC128709.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197458405,"end":197467105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279738.1","gene_symbol":"AL022311.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":37876148,"end":37895563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228501.2","gene_symbol":"RPL15P18","gene_name":"ribosomal protein L15 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728088","summary":null,"start":100150481,"end":100151092,"strand":-1,"description":"ribosomal protein L15 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36515]"}, {"versioned_ensembl_gene_id":"ENSG00000170516.16","gene_symbol":"COX7B2","gene_name":"cytochrome c oxidase subunit 7B2 [Source:HGNC Symbol;Acc:HGNC:24381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"170712","summary":null,"start":46734827,"end":46909235,"strand":-1,"description":"cytochrome c oxidase subunit 7B2 [Source:HGNC Symbol;Acc:HGNC:24381]"}, {"versioned_ensembl_gene_id":"ENSG00000220890.3","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bQB115I13.2,bPG299F13.9,FLJ40123,bCX101P6.9","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31190191,"end":31196403,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000159792.9","gene_symbol":"PSKH1","gene_name":"protein serine kinase H1 [Source:HGNC Symbol;Acc:HGNC:9529]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5681","summary":null,"start":67893272,"end":67929678,"strand":1,"description":"protein serine kinase H1 [Source:HGNC Symbol;Acc:HGNC:9529]"}, {"versioned_ensembl_gene_id":"ENSG00000254718.6","gene_symbol":"AL157756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60240121,"end":60248765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263096.1","gene_symbol":"AC007638.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55271504,"end":55273653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281904.1","gene_symbol":"AC233263.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90365737,"end":90367699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265897.2","gene_symbol":"AC233263.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90359809,"end":90360032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226388.1","gene_symbol":"ELL2P4","gene_name":"elongation factor for RNA polymerase II 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39346]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128690","summary":null,"start":146553728,"end":146555765,"strand":1,"description":"elongation factor for RNA polymerase II 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39346]"}, {"versioned_ensembl_gene_id":"ENSG00000228191.1","gene_symbol":"AL512326.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179271116,"end":179271266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133328.3","gene_symbol":"HRASLS2","gene_name":"HRAS like suppressor 2 [Source:HGNC Symbol;Acc:HGNC:17824]","synonyms":"FLJ20556","biotype":"protein_coding","ncbi_id":"54979","summary":"The protein encoded by this gene has both phospholipase and acyltransferase activities and acts as a tumor suppressor. The encoded protein can hydrolyze dipalmitoylated phosphatidylcholine (PC) to palmitic acid and lyso-PC. In addition, this protein can catalyze the N-acylation of phosphatidylethanolamine and can catalyze the O-acylation of lyso-PC to form PC. [provided by RefSeq, Jul 2016]","start":63552770,"end":63563383,"strand":-1,"description":"HRAS like suppressor 2 [Source:HGNC Symbol;Acc:HGNC:17824]"}, {"versioned_ensembl_gene_id":"ENSG00000228325.5","gene_symbol":"IGKV3D-7","gene_name":"immunoglobulin kappa variable 3D-7 [Source:HGNC Symbol;Acc:HGNC:5829]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28877","summary":null,"start":90234812,"end":90235370,"strand":1,"description":"immunoglobulin kappa variable 3D-7 [Source:HGNC Symbol;Acc:HGNC:5829]"}, {"versioned_ensembl_gene_id":"ENSG00000124608.4","gene_symbol":"AARS2","gene_name":"alanyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21022]","synonyms":"KIAA1270,bA444E17.1,AARSL","biotype":"protein_coding","ncbi_id":"57505","summary":"The protein encoded by this gene belongs to the class-II aminoacyl-tRNA synthetase family. Aminoacyl-tRNA synthetases play critical roles in mRNA translation by charging tRNAs with their cognate amino acids. The encoded protein is a mitochondrial enzyme that specifically aminoacylates alanyl-tRNA. Mutations in this gene are a cause of combined oxidative phosphorylation deficiency 8. [provided by RefSeq, Dec 2011]","start":44299654,"end":44313326,"strand":-1,"description":"alanyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21022]"}, {"versioned_ensembl_gene_id":"ENSG00000282229.1","gene_symbol":"AC131056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36183253,"end":36196508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221870.2","gene_symbol":"TMEM257","gene_name":"transmembrane protein 257 [Source:HGNC Symbol;Acc:HGNC:2562]","synonyms":"CXorf1","biotype":"protein_coding","ncbi_id":"9142","summary":null,"start":145827410,"end":145829850,"strand":1,"description":"transmembrane protein 257 [Source:HGNC Symbol;Acc:HGNC:2562]"}, {"versioned_ensembl_gene_id":"ENSG00000250532.1","gene_symbol":"AC021180.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74418917,"end":74440457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217372.2","gene_symbol":"TUBB4BP7","gene_name":"tubulin beta 4B class IVb pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42337]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442271","summary":null,"start":152898047,"end":152899280,"strand":1,"description":"tubulin beta 4B class IVb pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42337]"}, {"versioned_ensembl_gene_id":"ENSG00000159461.14","gene_symbol":"AMFR","gene_name":"autocrine motility factor receptor [Source:HGNC Symbol;Acc:HGNC:463]","synonyms":"RNF45,gp78","biotype":"protein_coding","ncbi_id":"267","summary":"This locus encodes a glycosylated transmembrane receptor. Its ligand, autocrine motility factor, is a tumor motility-stimulating protein secreted by tumor cells. The encoded receptor is also a member of the E3 ubiquitin ligase family of proteins. It catalyzes ubiquitination and endoplasmic reticulum-associated degradation of specific proteins. [provided by RefSeq, Feb 2012]","start":56361452,"end":56425538,"strand":-1,"description":"autocrine motility factor receptor [Source:HGNC Symbol;Acc:HGNC:463]"}, {"versioned_ensembl_gene_id":"ENSG00000235744.11","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-D0-alpha,HLA-DZA,HLA-DNA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":32982126,"end":32987559,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000186645.7","gene_symbol":"SPDYE17","gene_name":"speedy/RINGO cell cycle regulator family member E17 [Source:HGNC Symbol;Acc:HGNC:51513]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723849","summary":null,"start":77024691,"end":77030572,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E17 [Source:HGNC Symbol;Acc:HGNC:51513]"}, {"versioned_ensembl_gene_id":"ENSG00000251334.2","gene_symbol":"AC020593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48936582,"end":48936880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149346.14","gene_symbol":"SLX4IP","gene_name":"SLX4 interacting protein [Source:HGNC Symbol;Acc:HGNC:16225]","synonyms":"dJ1099D15.3,C20orf94","biotype":"protein_coding","ncbi_id":"128710","summary":null,"start":10435303,"end":10636829,"strand":1,"description":"SLX4 interacting protein [Source:HGNC Symbol;Acc:HGNC:16225]"}, {"versioned_ensembl_gene_id":"ENSG00000242272.1","gene_symbol":"AK2P2","gene_name":"adenylate kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339736","summary":null,"start":31823413,"end":31823817,"strand":-1,"description":"adenylate kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33542]"}, {"versioned_ensembl_gene_id":"ENSG00000162704.15","gene_symbol":"ARPC5","gene_name":"actin related protein 2/3 complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:708]","synonyms":"p16-Arc,dJ127C7.3,ARC16","biotype":"protein_coding","ncbi_id":"10092","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p16 subunit, has yet to be determined. Alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":183620846,"end":183635757,"strand":-1,"description":"actin related protein 2/3 complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:708]"}, {"versioned_ensembl_gene_id":"ENSG00000255059.1","gene_symbol":"AP000620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100666459,"end":100666962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260494.1","gene_symbol":"AC002310.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30537202,"end":30538231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245281.6","gene_symbol":"AC124242.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18084868,"end":18096394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279320.1","gene_symbol":"AC069528.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":146504570,"end":146506560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231705.1","gene_symbol":"AL451069.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132419083,"end":132420953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234165.1","gene_symbol":"AC114877.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26712307,"end":26713364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233338.1","gene_symbol":"TLR8-AS1","gene_name":"TLR8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40720]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"349408","summary":null,"start":12902817,"end":12908333,"strand":-1,"description":"TLR8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40720]"}, {"versioned_ensembl_gene_id":"ENSG00000258875.5","gene_symbol":"AL135818.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":91242759,"end":91252211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275129.1","gene_symbol":"AC243994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121314947,"end":121315055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242529.1","gene_symbol":"AHCYP8","gene_name":"adenosylhomocysteinase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107063538","summary":null,"start":248721993,"end":248722201,"strand":-1,"description":"adenosylhomocysteinase pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45000]"}, {"versioned_ensembl_gene_id":"ENSG00000260719.1","gene_symbol":"AC009133.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29745247,"end":29748299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282593.1","gene_symbol":"IGHV3-53","gene_name":"immunoglobulin heavy variable 3-53 [Source:HGNC Symbol;Acc:HGNC:5610]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28420","summary":null,"start":106617357,"end":106618028,"strand":-1,"description":"immunoglobulin heavy variable 3-53 [Source:HGNC Symbol;Acc:HGNC:5610]"}, {"versioned_ensembl_gene_id":"ENSG00000187701.4","gene_symbol":"OR2T27","gene_name":"olfactory receptor family 2 subfamily T member 27 [Source:HGNC Symbol;Acc:HGNC:31252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403239","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248649838,"end":248655528,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 27 [Source:HGNC Symbol;Acc:HGNC:31252]"}, {"versioned_ensembl_gene_id":"ENSG00000101441.4","gene_symbol":"CST4","gene_name":"cystatin S [Source:HGNC Symbol;Acc:HGNC:2476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1472","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a type 2 salivary cysteine peptidase inhibitor. The protein is an S-type cystatin, based on its high level of expression in saliva, tears and seminal plasma. The specific role in these fluids is unclear but antibacterial and antiviral activity is present, consistent with a protective function. [provided by RefSeq, Jul 2008]","start":23685640,"end":23689040,"strand":-1,"description":"cystatin S [Source:HGNC Symbol;Acc:HGNC:2476]"}, {"versioned_ensembl_gene_id":"ENSG00000165526.8","gene_symbol":"RPUSD4","gene_name":"RNA pseudouridylate synthase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25898]","synonyms":"FLJ14494","biotype":"protein_coding","ncbi_id":"84881","summary":null,"start":126202094,"end":126211692,"strand":-1,"description":"RNA pseudouridylate synthase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25898]"}, {"versioned_ensembl_gene_id":"ENSG00000224324.1","gene_symbol":"THAP5P1","gene_name":"THAP domain containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285872","summary":null,"start":158623188,"end":158623449,"strand":-1,"description":"THAP domain containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22340]"}, {"versioned_ensembl_gene_id":"ENSG00000124380.10","gene_symbol":"SNRNP27","gene_name":"small nuclear ribonucleoprotein U4/U6.U5 subunit 27 [Source:HGNC Symbol;Acc:HGNC:30240]","synonyms":"U4/U6.U5-27K,RY1","biotype":"protein_coding","ncbi_id":"11017","summary":"This gene encodes a serine/arginine-rich (SR) protein. SR proteins play important roles in pre-mRNA splicing by facilitating the recognition and selection of splice sites. The encoded protein associates with the 25S U4/U6.U5 tri-snRNP, a major component of the U2-type spiceosome. The expression of this gene may be altered in cells infected with the human T-cell lymphotropic virus type 1 (HTLV-1) retrovirus. A pseudogene of this gene is located on the long arm of chromosome 5. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]","start":69893560,"end":69905575,"strand":1,"description":"small nuclear ribonucleoprotein U4/U6.U5 subunit 27 [Source:HGNC Symbol;Acc:HGNC:30240]"}, {"versioned_ensembl_gene_id":"ENSG00000198794.11","gene_symbol":"SCAMP5","gene_name":"secretory carrier membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:30386]","synonyms":"MGC24969","biotype":"protein_coding","ncbi_id":"192683","summary":null,"start":74957219,"end":75021496,"strand":1,"description":"secretory carrier membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:30386]"}, {"versioned_ensembl_gene_id":"ENSG00000203923.4","gene_symbol":"SPANXN1","gene_name":"SPANX family member N1 [Source:HGNC Symbol;Acc:HGNC:33174]","synonyms":"SPANX-N1,CT11.6","biotype":"protein_coding","ncbi_id":"494118","summary":"This gene represents one of several duplicated family members that are located on chromosome X. This gene family encodes proteins that play a role in spermiogenesis. These proteins represent a specific subgroup of cancer/testis-associated antigens, and they may be candidates for tumor vaccines. This family member belongs to a subgroup of related genes that are present in all primates and rats and mice, and thus, it represents one of the ancestral family members. [provided by RefSeq, May 2010]","start":145246828,"end":145256112,"strand":1,"description":"SPANX family member N1 [Source:HGNC Symbol;Acc:HGNC:33174]"}, {"versioned_ensembl_gene_id":"ENSG00000153317.14","gene_symbol":"ASAP1","gene_name":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:2720]","synonyms":"ZG14P,PAP,KIAA1249,DDEF1,CENTB4","biotype":"protein_coding","ncbi_id":"50807","summary":"This gene encodes an ADP-ribosylation factor (ARF) GTPase-activating protein. The GTPase-activating activity is stimulated by phosphatidylinositol 4,5-biphosphate (PIP2), and is greater towards ARF1 and ARF5, and lesser for ARF6. This gene maybe involved in regulation of membrane trafficking and cytoskeleton remodeling. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":130052104,"end":130443660,"strand":-1,"description":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:2720]"}, {"versioned_ensembl_gene_id":"ENSG00000136305.11","gene_symbol":"CIDEB","gene_name":"cell death-inducing DFFA-like effector b [Source:HGNC Symbol;Acc:HGNC:1977]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27141","summary":null,"start":24305096,"end":24311430,"strand":-1,"description":"cell death-inducing DFFA-like effector b [Source:HGNC Symbol;Acc:HGNC:1977]"}, {"versioned_ensembl_gene_id":"ENSG00000223717.1","gene_symbol":"DNAJA1P1","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39337]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129308","summary":null,"start":58751047,"end":58752233,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39337]"}, {"versioned_ensembl_gene_id":"ENSG00000040275.16","gene_symbol":"SPDL1","gene_name":"spindle apparatus coiled-coil protein 1 [Source:HGNC Symbol;Acc:HGNC:26010]","synonyms":"hSpindly,FLJ20364,CCDC99","biotype":"protein_coding","ncbi_id":"54908","summary":"This gene encodes a coiled-coil domain-containing protein that functions in mitotic spindle formation and chromosome segregation. The encoded protein plays a role in coordinating microtubule attachment by promoting recruitment of dynein proteins, and in mitotic checkpoint signaling. [provided by RefSeq, Jul 2016]","start":169583634,"end":169604778,"strand":1,"description":"spindle apparatus coiled-coil protein 1 [Source:HGNC Symbol;Acc:HGNC:26010]"}, {"versioned_ensembl_gene_id":"ENSG00000128609.14","gene_symbol":"NDUFA5","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 [Source:HGNC Symbol;Acc:HGNC:7688]","synonyms":"UQOR13,NUFM,CI-13KD-B,CI-13kB,B13","biotype":"protein_coding","ncbi_id":"4698","summary":"This nuclear gene encodes a conserved protein that comprises the B13 subunit of complex I of the mitochondrial respiratory chain. The encoded protein localizes to the inner mitochondrial membrane, where it is thought to aid in the transfer of electrons from NADH to ubiquinone. Alternative splicing results in multiple transcript variants. There are numerous pseudogenes of this gene on chromosomes 1, 3, 6, 8, 9, 11, 12, and 16. [provided by RefSeq, Apr 2014]","start":123536997,"end":123558255,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 [Source:HGNC Symbol;Acc:HGNC:7688]"}, {"versioned_ensembl_gene_id":"ENSG00000225365.1","gene_symbol":"AC078942.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158537495,"end":158539879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230817.5","gene_symbol":"LINC01362","gene_name":"long intergenic non-protein coding RNA 1362 [Source:HGNC Symbol;Acc:HGNC:50596]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103283057","summary":null,"start":82903183,"end":83166815,"strand":1,"description":"long intergenic non-protein coding RNA 1362 [Source:HGNC Symbol;Acc:HGNC:50596]"}, {"versioned_ensembl_gene_id":"ENSG00000257576.1","gene_symbol":"HSPD1P4","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35146]","synonyms":"HSPD1-5P","biotype":"processed_pseudogene","ncbi_id":"644745","summary":null,"start":56511002,"end":56512703,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35146]"}, {"versioned_ensembl_gene_id":"ENSG00000273673.2","gene_symbol":"RPL9P9","gene_name":"ribosomal protein L9 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17251]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":82451282,"end":82451992,"strand":-1,"description":"ribosomal protein L9 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17251]"}, {"versioned_ensembl_gene_id":"ENSG00000168116.13","gene_symbol":"KIAA1586","gene_name":"KIAA1586 [Source:HGNC Symbol;Acc:HGNC:21360]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57691","summary":null,"start":57046532,"end":57055239,"strand":1,"description":"KIAA1586 [Source:HGNC Symbol;Acc:HGNC:21360]"}, {"versioned_ensembl_gene_id":"ENSG00000265293.2","gene_symbol":"ARGFXP2","gene_name":"arginine-fifty homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503640","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the ARGFX homeobox gene family. [provided by RefSeq, Jul 2008]","start":32150433,"end":32151504,"strand":-1,"description":"arginine-fifty homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23977]"}, {"versioned_ensembl_gene_id":"ENSG00000262316.1","gene_symbol":"AC025283.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3323192,"end":3323925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189295.13","gene_symbol":"ANKRD62P1-PARP4P3","gene_name":"ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42393]","synonyms":"VWFP1-ANKRD62P1-PARP4P3","biotype":"processed_transcript","ncbi_id":"23783","summary":"This locus represents putative naturally-occurring readthrough transcription between two pseudogenes, ANKRD62P1 (ankyrin repeat domain 62 pseudogene 1) and PARP4P3 (poly(ADP-ribose) polymerase family member 4 pseudogene 3). The individual pseudogene loci are not curated as transcribed regions. The readthrough transcript would likely not encode a functional protein. [provided by RefSeq, Jan 2016]","start":16654066,"end":16675540,"strand":-1,"description":"ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42393]"}, {"versioned_ensembl_gene_id":"ENSG00000258343.1","gene_symbol":"AC090001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95795345,"end":95858839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173867.9","gene_symbol":"AC013489.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":88459717,"end":88511521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259494.1","gene_symbol":"MRPL46","gene_name":"mitochondrial ribosomal protein L46 [Source:HGNC Symbol;Acc:HGNC:1192]","synonyms":"P2ECSL,LIECG2,C15orf4","biotype":"protein_coding","ncbi_id":"26589","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":88459476,"end":88467419,"strand":-1,"description":"mitochondrial ribosomal protein L46 [Source:HGNC Symbol;Acc:HGNC:1192]"}, {"versioned_ensembl_gene_id":"ENSG00000254388.1","gene_symbol":"DUTP2","gene_name":"deoxyuridine triphosphatase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873909","summary":null,"start":123352181,"end":123352643,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39515]"}, {"versioned_ensembl_gene_id":"ENSG00000203321.2","gene_symbol":"C9orf41-AS1","gene_name":"C9orf41 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51188]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927380","summary":null,"start":74952968,"end":74996293,"strand":1,"description":"C9orf41 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51188]"}, {"versioned_ensembl_gene_id":"ENSG00000197471.11","gene_symbol":"SPN","gene_name":"sialophorin [Source:HGNC Symbol;Acc:HGNC:11249]","synonyms":"CD43,LSN,GPL115","biotype":"protein_coding","ncbi_id":"6693","summary":"This gene encodes a highly sialylated glycoprotein that functions in antigen-specific activation of T cells, and is found on the surface of thymocytes, T lymphocytes, monocytes, granulocytes, and some B lymphocytes. It contains a mucin-like extracellular domain, a transmembrane region and a carboxy-terminal intracellular region. The extracellular domain has a high proportion of serine and threonine residues, allowing extensive O-glycosylation, and has one potential N-glycosylation site, while the carboxy-terminal region has potential phosphorylation sites that may mediate transduction of activation signals. Different glycoforms of this protein have been described. In stimulated immune cells, proteolytic cleavage of the extracellular domain occurs in some cell types, releasing a soluble extracellular fragment. Defects in expression of this gene are associated with Wiskott-Aldrich syndrome. [provided by RefSeq, Sep 2017]","start":29662979,"end":29670876,"strand":1,"description":"sialophorin [Source:HGNC Symbol;Acc:HGNC:11249]"}, {"versioned_ensembl_gene_id":"ENSG00000088756.12","gene_symbol":"ARHGAP28","gene_name":"Rho GTPase activating protein 28 [Source:HGNC Symbol;Acc:HGNC:25509]","synonyms":"KIAA1314,FLJ10312","biotype":"protein_coding","ncbi_id":"79822","summary":null,"start":6729718,"end":6915716,"strand":1,"description":"Rho GTPase activating protein 28 [Source:HGNC Symbol;Acc:HGNC:25509]"}, {"versioned_ensembl_gene_id":"ENSG00000231156.1","gene_symbol":"AC093702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45013214,"end":45013668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136830.11","gene_symbol":"FAM129B","gene_name":"family with sequence similarity 129 member B [Source:HGNC Symbol;Acc:HGNC:25282]","synonyms":"MINERVA,FLJ22298,FLJ22151,FLJ13518,DKFZP434H0820,C9orf88,bA356B19.6","biotype":"protein_coding","ncbi_id":"64855","summary":null,"start":127505339,"end":127578989,"strand":-1,"description":"family with sequence similarity 129 member B [Source:HGNC Symbol;Acc:HGNC:25282]"}, {"versioned_ensembl_gene_id":"ENSG00000243316.7","gene_symbol":"GUCY2GP","gene_name":"guanylate cyclase 2G, pseudogene [Source:HGNC Symbol;Acc:HGNC:31863]","synonyms":"GUCY2G","biotype":"transcribed_unitary_pseudogene","ncbi_id":"390003","summary":null,"start":112308181,"end":112356574,"strand":-1,"description":"guanylate cyclase 2G, pseudogene [Source:HGNC Symbol;Acc:HGNC:31863]"}, {"versioned_ensembl_gene_id":"ENSG00000236664.1","gene_symbol":"AC011998.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":177953111,"end":178011989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278600.1","gene_symbol":"AC015871.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79920195,"end":79922455,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228113.7","gene_symbol":"AC003991.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88219359,"end":88304367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254003.1","gene_symbol":"AC003991.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88216660,"end":88219226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266379.6","gene_symbol":"AC090616.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32088160,"end":32094933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258781.2","gene_symbol":"AL589743.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19228924,"end":19244931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178741.11","gene_symbol":"COX5A","gene_name":"cytochrome c oxidase subunit 5A [Source:HGNC Symbol;Acc:HGNC:2267]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9377","summary":"Cytochrome c oxidase (COX) is the terminal enzyme of the mitochondrial respiratory chain. It is a multi-subunit enzyme complex that couples the transfer of electrons from cytochrome c to molecular oxygen and contributes to a proton electrochemical gradient across the inner mitochondrial membrane. The complex consists of 13 mitochondrial- and nuclear-encoded subunits. The mitochondrially-encoded subunits perform the electron transfer of proton pumping activities. The functions of the nuclear-encoded subunits are unknown but they may play a role in the regulation and assembly of the complex. This gene encodes the nuclear-encoded subunit Va of the human mitochondrial respiratory chain enzyme. A pseudogene COX5AP1 has been found in chromosome 14q22. [provided by RefSeq, Jul 2008]","start":74919791,"end":74938168,"strand":-1,"description":"cytochrome c oxidase subunit 5A [Source:HGNC Symbol;Acc:HGNC:2267]"}, {"versioned_ensembl_gene_id":"ENSG00000006744.18","gene_symbol":"ELAC2","gene_name":"elaC ribonuclease Z 2 [Source:HGNC Symbol;Acc:HGNC:14198]","synonyms":"HPC2,FLJ10530","biotype":"protein_coding","ncbi_id":"60528","summary":"The protein encoded by this gene has a C-terminal domain with tRNA 3′ processing endoribonuclease activity, which catalyzes the removal of the 3' trailer from precursor tRNAs. The protein also interacts with activated Smad family member 2 (Smad2) and its nuclear partner forkhead box H1 (also known as FAST-1), and reduced expression can suppress transforming growth factor-beta induced growth arrest. Mutations in this gene result in an increased risk of prostate cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":12992391,"end":13018187,"strand":-1,"description":"elaC ribonuclease Z 2 [Source:HGNC Symbol;Acc:HGNC:14198]"}, {"versioned_ensembl_gene_id":"ENSG00000230871.1","gene_symbol":"RPS6P23","gene_name":"ribosomal protein S6 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39581]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130313","summary":null,"start":99173593,"end":99174490,"strand":1,"description":"ribosomal protein S6 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39581]"}, {"versioned_ensembl_gene_id":"ENSG00000167685.14","gene_symbol":"ZNF444","gene_name":"zinc finger protein 444 [Source:HGNC Symbol;Acc:HGNC:16052]","synonyms":"ZSCAN17,FLJ11137,EZF2","biotype":"protein_coding","ncbi_id":"55311","summary":"This gene encodes a zinc finger protein which activates transcription of a scavenger receptor gene involved in the degradation of acetylated low density lipoprotein (Ac-LDL) (PMID: 11978792). This gene is located in a cluster of zinc finger genes on chromosome 19 at q13.4. A pseudogene of this gene is located on chromosome 15. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":56132599,"end":56160893,"strand":1,"description":"zinc finger protein 444 [Source:HGNC Symbol;Acc:HGNC:16052]"}, {"versioned_ensembl_gene_id":"ENSG00000282357.1","gene_symbol":"AC240137.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":323447,"end":324508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260992.1","gene_symbol":"DOCK9-AS2","gene_name":"DOCK9 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43696]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861541","summary":null,"start":99087819,"end":99088625,"strand":1,"description":"DOCK9 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43696]"}, {"versioned_ensembl_gene_id":"ENSG00000213851.3","gene_symbol":"AC098590.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43410041,"end":43410937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011590.13","gene_symbol":"ZBTB32","gene_name":"zinc finger and BTB domain containing 32 [Source:HGNC Symbol;Acc:HGNC:16763]","synonyms":"ZNF538,TZFP,Rog,FAZF,FAXF","biotype":"protein_coding","ncbi_id":"27033","summary":null,"start":35704527,"end":35717038,"strand":1,"description":"zinc finger and BTB domain containing 32 [Source:HGNC Symbol;Acc:HGNC:16763]"}, {"versioned_ensembl_gene_id":"ENSG00000277096.1","gene_symbol":"AC098590.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43388157,"end":43388437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267190.1","gene_symbol":"TYMSP2","gene_name":"thymidylate synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729122","summary":null,"start":35683778,"end":35684201,"strand":-1,"description":"thymidylate synthetase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52352]"}, {"versioned_ensembl_gene_id":"ENSG00000279959.1","gene_symbol":"AC024580.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56127236,"end":56127466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275886.2","gene_symbol":"AC129507.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":333260,"end":335543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282336.1","gene_symbol":"AC129507.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":354693,"end":359636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215203.2","gene_symbol":"GRXCR1","gene_name":"glutaredoxin and cysteine rich domain containing 1 [Source:HGNC Symbol;Acc:HGNC:31673]","synonyms":"PPP1R88,DFNB25","biotype":"protein_coding","ncbi_id":"389207","summary":"This gene is one of 60 loci associated with autosomal-recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX-like domains; these domains play a role in the S-glutathionylation of proteins and may be involved in actin organization in hair cells. [provided by RefSeq, Sep 2010]","start":42893267,"end":43030658,"strand":1,"description":"glutaredoxin and cysteine rich domain containing 1 [Source:HGNC Symbol;Acc:HGNC:31673]"}, {"versioned_ensembl_gene_id":"ENSG00000105668.7","gene_symbol":"UPK1A","gene_name":"uroplakin 1A [Source:HGNC Symbol;Acc:HGNC:12577]","synonyms":"TSPAN21","biotype":"protein_coding","ncbi_id":"11045","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is found in the asymmetrical unit membrane (AUM) where it can complex with other transmembrane 4 superfamily proteins. It may play a role in normal bladder epithelial physiology, possibly in regulating membrane permeability of superficial umbrella cells or in stabilizing the apical membrane through AUM/cytoskeletal interactions. The protein may also play a role in tumor suppression. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":35666516,"end":35678483,"strand":1,"description":"uroplakin 1A [Source:HGNC Symbol;Acc:HGNC:12577]"}, {"versioned_ensembl_gene_id":"ENSG00000237145.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32860339,"end":32861169,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000226673.2","gene_symbol":"LINC01108","gene_name":"long intergenic non-protein coding RNA 1108 [Source:HGNC Symbol;Acc:HGNC:49234]","synonyms":"LncRNA-ES1","biotype":"lincRNA","ncbi_id":"102216342","summary":null,"start":14280127,"end":14285454,"strand":-1,"description":"long intergenic non-protein coding RNA 1108 [Source:HGNC Symbol;Acc:HGNC:49234]"}, {"versioned_ensembl_gene_id":"ENSG00000178104.19","gene_symbol":"PDE4DIP","gene_name":"phosphodiesterase 4D interacting protein [Source:HGNC Symbol;Acc:HGNC:15580]","synonyms":"MMGL,KIAA0477,KIAA0454,CMYA2","biotype":"protein_coding","ncbi_id":"9659","summary":"The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]","start":148808181,"end":149048286,"strand":1,"description":"phosphodiesterase 4D interacting protein [Source:HGNC Symbol;Acc:HGNC:15580]"}, {"versioned_ensembl_gene_id":"ENSG00000106609.16","gene_symbol":"TMEM248","gene_name":"transmembrane protein 248 [Source:HGNC Symbol;Acc:HGNC:25476]","synonyms":"FLJ13090,FLJ10099,C7orf42","biotype":"protein_coding","ncbi_id":"55069","summary":null,"start":66921225,"end":66958551,"strand":1,"description":"transmembrane protein 248 [Source:HGNC Symbol;Acc:HGNC:25476]"}, {"versioned_ensembl_gene_id":"ENSG00000231356.1","gene_symbol":"AL157698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66360766,"end":66361776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232546.1","gene_symbol":"AC027644.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66848496,"end":66858136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269955.2","gene_symbol":"C7orf55-LUC7L2","gene_name":"C7orf55-LUC7L2 readthrough [Source:HGNC Symbol;Acc:HGNC:44671]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100996928","summary":"This locus represents naturally occurring readthrough transcription between the neighboring C7orf55 (chromosome 7 open reading frame 55) and LUC7L2 (LUC7-like 2) genes on chromosome 7. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jul 2012]","start":139341360,"end":139422599,"strand":1,"description":"C7orf55-LUC7L2 readthrough [Source:HGNC Symbol;Acc:HGNC:44671]"}, {"versioned_ensembl_gene_id":"ENSG00000231484.1","gene_symbol":"AC023141.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57828331,"end":57837046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136159.3","gene_symbol":"NUDT15","gene_name":"nudix hydrolase 15 [Source:HGNC Symbol;Acc:HGNC:23063]","synonyms":"MTH2,FLJ10956","biotype":"protein_coding","ncbi_id":"55270","summary":"This gene encodes an enzyme that belongs to the Nudix hydrolase superfamily. Members of this superfamily catalyze the hydrolysis of nucleoside diphosphates, including substrates like 8-oxo-dGTP, which are a result of oxidative damage, and can induce base mispairing during DNA replication, causing transversions. The encoded enzyme is a negative regulator of thiopurine activation and toxicity. Mutations in this gene result in poor metabolism of thiopurines, and are associated with thiopurine-induced early leukopenia. Multiple pseudogenes of this gene have been identified. [provided by RefSeq, Apr 2016]","start":48037567,"end":48047222,"strand":1,"description":"nudix hydrolase 15 [Source:HGNC Symbol;Acc:HGNC:23063]"}, {"versioned_ensembl_gene_id":"ENSG00000276968.1","gene_symbol":"AL158196.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48041751,"end":48042184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259994.1","gene_symbol":"AL353796.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":30302826,"end":30306066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248243.1","gene_symbol":"LINC02014","gene_name":"long intergenic non-protein coding RNA 2014 [Source:HGNC Symbol;Acc:HGNC:52849]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374105","summary":null,"start":130089433,"end":130094304,"strand":-1,"description":"long intergenic non-protein coding RNA 2014 [Source:HGNC Symbol;Acc:HGNC:52849]"}, {"versioned_ensembl_gene_id":"ENSG00000275381.1","gene_symbol":"AC019206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69844509,"end":69844933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119559.15","gene_symbol":"C19orf25","gene_name":"chromosome 19 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:26711]","synonyms":"FLJ36666","biotype":"protein_coding","ncbi_id":"148223","summary":null,"start":1461143,"end":1479556,"strand":-1,"description":"chromosome 19 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:26711]"}, {"versioned_ensembl_gene_id":"ENSG00000198601.3","gene_symbol":"OR2M2","gene_name":"olfactory receptor family 2 subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:8268]","synonyms":"OST423,OR2M2Q","biotype":"protein_coding","ncbi_id":"391194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248174821,"end":248181067,"strand":1,"description":"olfactory receptor family 2 subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:8268]"}, {"versioned_ensembl_gene_id":"ENSG00000249846.6","gene_symbol":"LINC02021","gene_name":"long intergenic non-protein coding RNA 2021 [Source:HGNC Symbol;Acc:HGNC:52856]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374104","summary":null,"start":130112550,"end":130120579,"strand":1,"description":"long intergenic non-protein coding RNA 2021 [Source:HGNC Symbol;Acc:HGNC:52856]"}, {"versioned_ensembl_gene_id":"ENSG00000111348.8","gene_symbol":"ARHGDIB","gene_name":"Rho GDP dissociation inhibitor beta [Source:HGNC Symbol;Acc:HGNC:679]","synonyms":"RhoGDI2,RAP1GN1,Ly-GDI,GDID4,GDIA2","biotype":"protein_coding","ncbi_id":"397","summary":"Members of the Rho (or ARH) protein family (see MIM 165390) and other Ras-related small GTP-binding proteins (see MIM 179520) are involved in diverse cellular events, including cell signaling, proliferation, cytoskeletal organization, and secretion. The GTP-binding proteins are active only in the GTP-bound state. At least 3 classes of proteins tightly regulate cycling between the GTP-bound and GDP-bound states: GTPase-activating proteins (GAPs), guanine nucleotide-releasing factors (GRFs), and GDP-dissociation inhibitors (GDIs). The GDIs, including ARHGDIB, decrease the rate of GDP dissociation from Ras-like GTPases (summary by Scherle et al., 1993 [PubMed 8356058]).[supplied by OMIM, Dec 2010]","start":14942017,"end":14961728,"strand":-1,"description":"Rho GDP dissociation inhibitor beta [Source:HGNC Symbol;Acc:HGNC:679]"}, {"versioned_ensembl_gene_id":"ENSG00000109471.4","gene_symbol":"IL2","gene_name":"interleukin 2 [Source:HGNC Symbol;Acc:HGNC:6001]","synonyms":"TCGF,IL-2","biotype":"protein_coding","ncbi_id":"3558","summary":"This gene is a member of the interleukin 2 (IL2) cytokine subfamily which includes IL4, IL7, IL9, IL15, IL21, erythropoietin, and thrombopoietin. The protein encoded by this gene is a secreted cytokine produced by activated CD4+ and CD8+ T lymphocytes, that is important for the proliferation of T and B lymphocytes. The receptor of this cytokine (IL2R) is a heterotrimeric protein complex whose gamma chain is also shared by IL4 and IL7. The expression of this gene in mature thymocytes is monoallelic, which represents an unusual regulatory mode for controlling the precise expression of a single gene. The targeted disruption of a similar gene in mice leads to ulcerative colitis-like disease, which suggests an essential role of this gene in the immune response to antigenic stimuli. [provided by RefSeq, Sep 2020]","start":122451470,"end":122456725,"strand":-1,"description":"interleukin 2 [Source:HGNC Symbol;Acc:HGNC:6001]"}, {"versioned_ensembl_gene_id":"ENSG00000177233.2","gene_symbol":"OR2M1P","gene_name":"olfactory receptor family 2 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8267]","synonyms":"OST037,OR2M1","biotype":"unprocessed_pseudogene","ncbi_id":"388762","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248121932,"end":248122882,"strand":1,"description":"olfactory receptor family 2 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8267]"}, {"versioned_ensembl_gene_id":"ENSG00000234270.1","gene_symbol":"RPL36P20","gene_name":"ribosomal protein L36 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:44564]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729032","summary":null,"start":41955445,"end":41955763,"strand":1,"description":"ribosomal protein L36 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:44564]"}, {"versioned_ensembl_gene_id":"ENSG00000259642.2","gene_symbol":"ST20-AS1","gene_name":"ST20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27521]","synonyms":"FLJ33788,C15orf37","biotype":"antisense_RNA","ncbi_id":"283687","summary":null,"start":79922771,"end":79926993,"strand":1,"description":"ST20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27521]"}, {"versioned_ensembl_gene_id":"ENSG00000160007.18","gene_symbol":"ARHGAP35","gene_name":"Rho GTPase activating protein 35 [Source:HGNC Symbol;Acc:HGNC:4591]","synonyms":"GRLF1,GRF-1,p190RhoGAP,p190ARhoGAP,P190A,KIAA1722","biotype":"protein_coding","ncbi_id":"2909","summary":"The human glucocorticoid receptor DNA binding factor, which associates with the promoter region of the glucocorticoid receptor gene (hGR gene), is a repressor of glucocorticoid receptor transcription. The amino acid sequence deduced from the cDNA sequences show the presence of three sequence motifs characteristic of a zinc finger and one motif suggestive of a leucine zipper in which 1 cysteine is found instead of all leucines. The GRLF1 enhances the homologous down-regulation of wild-type hGR gene expression. Biochemical analysis suggests that GRLF1 interaction is sequence specific and that transcriptional efficacy of GRLF1 is regulated through its interaction with specific sequence motif. The level of expression is regulated by glucocorticoids. [provided by RefSeq, Jul 2008]","start":46918676,"end":47005077,"strand":1,"description":"Rho GTPase activating protein 35 [Source:HGNC Symbol;Acc:HGNC:4591]"}, {"versioned_ensembl_gene_id":"ENSG00000259332.3","gene_symbol":"ST20-MTHFS","gene_name":"ST20-MTHFS readthrough [Source:HGNC Symbol;Acc:HGNC:44655]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528021","summary":"This locus represents naturally occurring read-through transcription between the neighboring suppressor of tumorigenicity 20 and 5,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase) genes on chromosome 15. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010]","start":79845150,"end":79923754,"strand":-1,"description":"ST20-MTHFS readthrough [Source:HGNC Symbol;Acc:HGNC:44655]"}, {"versioned_ensembl_gene_id":"ENSG00000236308.1","gene_symbol":"AL138921.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100190036,"end":100190747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237492.1","gene_symbol":"OR2L9P","gene_name":"olfactory receptor family 2 subfamily L member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15015]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81462","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247974741,"end":247975653,"strand":1,"description":"olfactory receptor family 2 subfamily L member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:15015]"}, {"versioned_ensembl_gene_id":"ENSG00000267489.3","gene_symbol":"LINC01837","gene_name":"long intergenic non-protein coding RNA 1837 [Source:HGNC Symbol;Acc:HGNC:52653]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372363","summary":null,"start":31859103,"end":32072082,"strand":-1,"description":"long intergenic non-protein coding RNA 1837 [Source:HGNC Symbol;Acc:HGNC:52653]"}, {"versioned_ensembl_gene_id":"ENSG00000275585.2","gene_symbol":"AC241377.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":120985692,"end":121052167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281741.2","gene_symbol":"AC241377.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":120913151,"end":120914238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197724.10","gene_symbol":"PHF2","gene_name":"PHD finger protein 2 [Source:HGNC Symbol;Acc:HGNC:8920]","synonyms":"KIAA0662,KDM7C,JHDM1E,CENP-35","biotype":"protein_coding","ncbi_id":"5253","summary":"This gene encodes a protein which contains a zinc finger-like PHD (plant homeodomain) finger, distinct from other classes of zinc finger motifs, and a hydrophobic and highly conserved domain. The PHD finger shows the typical Cys4-His-Cys3 arrangement. PHD finger genes are thought to belong to a diverse group of transcriptional regulators possibly affecting eukaryotic gene expression by influencing chromatin structure. [provided by RefSeq, Jul 2008]","start":93576407,"end":93679587,"strand":1,"description":"PHD finger protein 2 [Source:HGNC Symbol;Acc:HGNC:8920]"}, {"versioned_ensembl_gene_id":"ENSG00000162961.13","gene_symbol":"DPY30","gene_name":"dpy-30, histone methyltransferase complex regulatory subunit [Source:HGNC Symbol;Acc:HGNC:24590]","synonyms":"Saf19,HDPY-30,Cps25","biotype":"protein_coding","ncbi_id":"84661","summary":"This gene encodes an integral core subunit of the SET1/MLL family of H3K4 methyltransferases. The encoded protein directly controls cell cycle regulators and plays an important role in the proliferation and differentiation of human hematopoietic progenitor cells. [provided by RefSeq, Mar 2016]","start":31867809,"end":32039812,"strand":-1,"description":"dpy-30, histone methyltransferase complex regulatory subunit [Source:HGNC Symbol;Acc:HGNC:24590]"}, {"versioned_ensembl_gene_id":"ENSG00000173335.4","gene_symbol":"CST9","gene_name":"cystatin 9 [Source:HGNC Symbol;Acc:HGNC:13261]","synonyms":"CTES7A,CLM","biotype":"protein_coding","ncbi_id":"128822","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a secreted protein that may play a role in hematopoietic differentiation or inflammation. [provided by RefSeq, Jul 2008]","start":23602410,"end":23605876,"strand":-1,"description":"cystatin 9 [Source:HGNC Symbol;Acc:HGNC:13261]"}, {"versioned_ensembl_gene_id":"ENSG00000042753.11","gene_symbol":"AP2S1","gene_name":"adaptor related protein complex 2 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:565]","synonyms":"HHC3,FBHOk,FBH3,CLAPS2","biotype":"protein_coding","ncbi_id":"1175","summary":"One of two major clathrin-associated adaptor complexes, AP-2, is a heterotetramer which is associated with the plasma membrane. This complex is composed of two large chains, a medium chain, and a small chain. This gene encodes the small chain of this complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":46838136,"end":46850992,"strand":-1,"description":"adaptor related protein complex 2 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:565]"}, {"versioned_ensembl_gene_id":"ENSG00000243593.1","gene_symbol":"LINC02049","gene_name":"long intergenic non-protein coding RNA 2049 [Source:HGNC Symbol;Acc:HGNC:52889]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926983","summary":null,"start":120833440,"end":120836360,"strand":-1,"description":"long intergenic non-protein coding RNA 2049 [Source:HGNC Symbol;Acc:HGNC:52889]"}, {"versioned_ensembl_gene_id":"ENSG00000213371.4","gene_symbol":"NAP1L1P3","gene_name":"nucleosome assembly protein 1 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130335","summary":null,"start":120805866,"end":120806745,"strand":1,"description":"nucleosome assembly protein 1 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38007]"}, {"versioned_ensembl_gene_id":"ENSG00000235232.1","gene_symbol":"MRPS18BP2","gene_name":"mitochondrial ribosomal protein S18B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359763","summary":null,"start":139668547,"end":139669305,"strand":1,"description":"mitochondrial ribosomal protein S18B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29742]"}, {"versioned_ensembl_gene_id":"ENSG00000283434.1","gene_symbol":"AC108750.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":88338413,"end":88467562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188672.17","gene_symbol":"RHCE","gene_name":"Rh blood group CcEe antigens [Source:HGNC Symbol;Acc:HGNC:10008]","synonyms":"RH,CD240CE","biotype":"protein_coding","ncbi_id":"6006","summary":"The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Aug 2016]","start":25362249,"end":25430192,"strand":-1,"description":"Rh blood group CcEe antigens [Source:HGNC Symbol;Acc:HGNC:10008]"}, {"versioned_ensembl_gene_id":"ENSG00000136535.14","gene_symbol":"TBR1","gene_name":"T-box, brain 1 [Source:HGNC Symbol;Acc:HGNC:11590]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10716","summary":"This gene is a member of a conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of numerous developmental processes. In mouse, the ortholog of this gene is expressed in the cerebral cortex, hippocampus, amygdala and olfactory bulb and is thought to play an important role in neuronal migration and axonal projection. In mouse, the C-terminal region of this protein was found to be necessary and sufficient for association with the guanylate kinase domain of calcium/calmodulin-dependent serine protein kinase. [provided by RefSeq, Dec 2015]","start":161416094,"end":161425870,"strand":1,"description":"T-box, brain 1 [Source:HGNC Symbol;Acc:HGNC:11590]"}, {"versioned_ensembl_gene_id":"ENSG00000162722.8","gene_symbol":"TRIM58","gene_name":"tripartite motif containing 58 [Source:HGNC Symbol;Acc:HGNC:24150]","synonyms":"BIA2","biotype":"protein_coding","ncbi_id":"25893","summary":null,"start":247857199,"end":247878205,"strand":1,"description":"tripartite motif containing 58 [Source:HGNC Symbol;Acc:HGNC:24150]"}, {"versioned_ensembl_gene_id":"ENSG00000206532.2","gene_symbol":"AC117402.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110888384,"end":110893476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235716.1","gene_symbol":"KRT18P46","gene_name":"keratin 18 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:33416]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391458","summary":null,"start":161580072,"end":161581350,"strand":1,"description":"keratin 18 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:33416]"}, {"versioned_ensembl_gene_id":"ENSG00000237007.4","gene_symbol":"KRT18P52","gene_name":"keratin 18 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:37888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418769","summary":null,"start":31822591,"end":31823436,"strand":-1,"description":"keratin 18 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:37888]"}, {"versioned_ensembl_gene_id":"ENSG00000239285.7","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31659349,"end":31663777,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000257432.1","gene_symbol":"AL512310.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19629006,"end":19630340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242993.1","gene_symbol":"AP000870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95963219,"end":95963624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160959.7","gene_symbol":"LRRC14","gene_name":"leucine rich repeat containing 14 [Source:HGNC Symbol;Acc:HGNC:20419]","synonyms":"LRRC14A,KIAA0014","biotype":"protein_coding","ncbi_id":"9684","summary":"This gene encodes a leucine-rich repeat-containing protein. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":144517992,"end":144525178,"strand":1,"description":"leucine rich repeat containing 14 [Source:HGNC Symbol;Acc:HGNC:20419]"}, {"versioned_ensembl_gene_id":"ENSG00000275862.1","gene_symbol":"AC008622.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46809583,"end":46810182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254402.6","gene_symbol":"LRRC24","gene_name":"leucine rich repeat containing 24 [Source:HGNC Symbol;Acc:HGNC:28947]","synonyms":"LRRC14OS","biotype":"protein_coding","ncbi_id":"441381","summary":null,"start":144522377,"end":144527032,"strand":-1,"description":"leucine rich repeat containing 24 [Source:HGNC Symbol;Acc:HGNC:28947]"}, {"versioned_ensembl_gene_id":"ENSG00000261332.1","gene_symbol":"AC116348.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30498766,"end":30499554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250623.1","gene_symbol":"AL136360.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2139673,"end":2141058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214367.7","gene_symbol":"HAUS3","gene_name":"HAUS augmin like complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:28719]","synonyms":"MGC4701,IT1,dgt3,C4orf15","biotype":"protein_coding","ncbi_id":"79441","summary":"This gene encodes a component of the HAUS augmin-like protein complex, which plays a key role in cytokinesis and mitosis. Disruption of the encoded protein causes mitotic defects resulting from fragmentation of centrosomes and microtubule destabilization. This gene shares its 5' exons with some transcripts from overlapping GeneID: 353497, which encodes a DNA polymerase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":2227464,"end":2242164,"strand":-1,"description":"HAUS augmin like complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:28719]"}, {"versioned_ensembl_gene_id":"ENSG00000205959.3","gene_symbol":"AC105345.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8482270,"end":8512610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280984.1","gene_symbol":"AL049748.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35685940,"end":35689373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277894.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000103522.15","gene_symbol":"IL21R","gene_name":"interleukin 21 receptor [Source:HGNC Symbol;Acc:HGNC:6006]","synonyms":"CD360","biotype":"protein_coding","ncbi_id":"50615","summary":"The protein encoded by this gene is a cytokine receptor for interleukin 21 (IL21). It belongs to the type I cytokine receptors, and has been shown to form a heterodimeric receptor complex with the common gamma-chain, a receptor subunit also shared by the receptors for interleukin 2, 4, 7, 9, and 15. This receptor transduces the growth promoting signal of IL21, and is important for the proliferation and differentiation of T cells, B cells, and natural killer (NK) cells. The ligand binding of this receptor leads to the activation of multiple downstream signaling molecules, including JAK1, JAK3, STAT1, and STAT3. Knockout studies of a similar gene in mouse suggest a role for this gene in regulating immunoglobulin production. Three alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2010]","start":27402162,"end":27452042,"strand":1,"description":"interleukin 21 receptor [Source:HGNC Symbol;Acc:HGNC:6006]"}, {"versioned_ensembl_gene_id":"ENSG00000248459.1","gene_symbol":"AC083906.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129998531,"end":129998936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260762.1","gene_symbol":"ACSM5P1","gene_name":"acyl-CoA synthetase medium-chain family member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51295]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421779","summary":null,"start":20586550,"end":20607107,"strand":-1,"description":"acyl-CoA synthetase medium-chain family member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51295]"}, {"versioned_ensembl_gene_id":"ENSG00000274347.1","gene_symbol":"AC127381.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19955300,"end":19955602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214380.4","gene_symbol":"AC068781.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109915976,"end":109916940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152661.7","gene_symbol":"GJA1","gene_name":"gap junction protein alpha 1 [Source:HGNC Symbol;Acc:HGNC:4274]","synonyms":"CX43,SDTY3,ODOD,ODDD,ODD,GJAL","biotype":"protein_coding","ncbi_id":"2697","summary":"This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014]","start":121435692,"end":121449727,"strand":1,"description":"gap junction protein alpha 1 [Source:HGNC Symbol;Acc:HGNC:4274]"}, {"versioned_ensembl_gene_id":"ENSG00000168875.2","gene_symbol":"SOX14","gene_name":"SRY-box 14 [Source:HGNC Symbol;Acc:HGNC:11193]","synonyms":"SOX28","biotype":"protein_coding","ncbi_id":"8403","summary":"This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome. [provided by RefSeq, Jul 2008]","start":137764284,"end":137766338,"strand":1,"description":"SRY-box 14 [Source:HGNC Symbol;Acc:HGNC:11193]"}, {"versioned_ensembl_gene_id":"ENSG00000230942.1","gene_symbol":"HMGN1P5","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39348]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874429","summary":null,"start":158266753,"end":158267320,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39348]"}, {"versioned_ensembl_gene_id":"ENSG00000267501.1","gene_symbol":"AC104365.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58754859,"end":58757842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240666.2","gene_symbol":"MME-AS1","gene_name":"MME antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40376]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873918","summary":null,"start":155158370,"end":155183285,"strand":-1,"description":"MME antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40376]"}, {"versioned_ensembl_gene_id":"ENSG00000105982.16","gene_symbol":"RNF32","gene_name":"ring finger protein 32 [Source:HGNC Symbol;Acc:HGNC:17118]","synonyms":"LMBR2,HSD15,FKSG33","biotype":"protein_coding","ncbi_id":"140545","summary":"The protein encoded by this gene contains two RING ring finger motifs. RING finger motifs are present in a variety of functionally distinct proteins and are known to be involved in protein-DNA or protein-protein interactions. This gene was found to be expressed during spermatogenesis, most likely in spermatocytes and/or in spermatids. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":156640281,"end":156677130,"strand":1,"description":"ring finger protein 32 [Source:HGNC Symbol;Acc:HGNC:17118]"}, {"versioned_ensembl_gene_id":"ENSG00000149742.9","gene_symbol":"SLC22A9","gene_name":"solute carrier family 22 member 9 [Source:HGNC Symbol;Acc:HGNC:16261]","synonyms":"UST3,OAT7,OAT4,FLJ23666","biotype":"protein_coding","ncbi_id":"114571","summary":null,"start":63369789,"end":63410294,"strand":1,"description":"solute carrier family 22 member 9 [Source:HGNC Symbol;Acc:HGNC:16261]"}, {"versioned_ensembl_gene_id":"ENSG00000231905.2","gene_symbol":"SETP10","gene_name":"SET pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287822","summary":null,"start":179183734,"end":179184547,"strand":1,"description":"SET pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42929]"}, {"versioned_ensembl_gene_id":"ENSG00000282321.1","gene_symbol":"MTND1P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42102]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873172","summary":null,"start":46828117,"end":46828413,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42102]"}, {"versioned_ensembl_gene_id":"ENSG00000223647.1","gene_symbol":"LINC01946","gene_name":"long intergenic non-protein coding RNA 1946 [Source:HGNC Symbol;Acc:HGNC:52770]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374449","summary":null,"start":31793823,"end":31803980,"strand":-1,"description":"long intergenic non-protein coding RNA 1946 [Source:HGNC Symbol;Acc:HGNC:52770]"}, {"versioned_ensembl_gene_id":"ENSG00000144840.8","gene_symbol":"RABL3","gene_name":"RAB, member of RAS oncogene family like 3 [Source:HGNC Symbol;Acc:HGNC:18072]","synonyms":"MGC23920","biotype":"protein_coding","ncbi_id":"285282","summary":null,"start":120686681,"end":120742993,"strand":-1,"description":"RAB, member of RAS oncogene family like 3 [Source:HGNC Symbol;Acc:HGNC:18072]"}, {"versioned_ensembl_gene_id":"ENSG00000260187.2","gene_symbol":"AC009101.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64735925,"end":64737283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250643.1","gene_symbol":"AC083906.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129954105,"end":129969294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273313.1","gene_symbol":"RBAKDN","gene_name":"RBAK downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33770]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389458","summary":null,"start":5072125,"end":5073223,"strand":1,"description":"RBAK downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33770]"}, {"versioned_ensembl_gene_id":"ENSG00000178381.11","gene_symbol":"ZFAND2A","gene_name":"zinc finger AN1-type containing 2A [Source:HGNC Symbol;Acc:HGNC:28073]","synonyms":"AIRAP","biotype":"protein_coding","ncbi_id":"90637","summary":null,"start":1152071,"end":1160759,"strand":-1,"description":"zinc finger AN1-type containing 2A [Source:HGNC Symbol;Acc:HGNC:28073]"}, {"versioned_ensembl_gene_id":"ENSG00000267689.1","gene_symbol":"AC010525.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55705978,"end":55706172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225221.1","gene_symbol":"PLA2G12AP2","gene_name":"phospholipase A2 group XIIA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420281","summary":null,"start":38902387,"end":38902650,"strand":1,"description":"phospholipase A2 group XIIA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39249]"}, {"versioned_ensembl_gene_id":"ENSG00000226745.2","gene_symbol":"AL512599.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40132764,"end":40133448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156510.12","gene_symbol":"HKDC1","gene_name":"hexokinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23302]","synonyms":"FLJ37767,FLJ22761","biotype":"protein_coding","ncbi_id":"80201","summary":"This gene encodes a member of the hexokinase protein family. The encoded protein is involved in glucose metabolism, and reduced expression may be associated with gestational diabetes mellitus. High expression of this gene may also be associated with poor prognosis in hepatocarcinoma. [provided by RefSeq, Sep 2016]","start":69220303,"end":69267559,"strand":1,"description":"hexokinase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23302]"}, {"versioned_ensembl_gene_id":"ENSG00000132932.16","gene_symbol":"ATP8A2","gene_name":"ATPase phospholipid transporting 8A2 [Source:HGNC Symbol;Acc:HGNC:13533]","synonyms":"ML-1,ATPIB","biotype":"protein_coding","ncbi_id":"51761","summary":"The protein encoded by this gene is a member of the P4 ATPase family of proteins, which are thought to be involved in a process called lipid flipping, whereby phospholipids are translocated inwards from the exoplasmic leaflet to the cytosolic leaflet of the cell membrane, which aids in generating and maintaining asymmetry in membrane lipids. This protein is predicted to contain an E1 E2 ATPase, a haloacid dehalogenase-like hydrolase (HAD) domain, and multiple transmembrane domains. Associations between this protein and cell cycle control protein 50A are important for translocation of phosphatidylserine across membranes. Mutations in this gene have been associated with a syndrome (CAMRQ4) characterized by cerebellar ataxia and cognitive disabilities. In addition, a translocation breakpoint within this gene was observed in an individual with neurological dysfunction. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]","start":25372071,"end":26025851,"strand":1,"description":"ATPase phospholipid transporting 8A2 [Source:HGNC Symbol;Acc:HGNC:13533]"}, {"versioned_ensembl_gene_id":"ENSG00000272402.1","gene_symbol":"AL031775.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24706747,"end":24707151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004838.13","gene_symbol":"ZMYND10","gene_name":"zinc finger MYND-type containing 10 [Source:HGNC Symbol;Acc:HGNC:19412]","synonyms":"CILD22,BLU","biotype":"protein_coding","ncbi_id":"51364","summary":"This gene encodes a protein containing a MYND-type zinc finger domain that likely functions in assembly of the dynein motor. Mutations in this gene can cause primary ciliary dyskinesia. This gene is also considered a tumor suppressor gene and is often mutated, deleted, or hypermethylated and silenced in cancer cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":50341110,"end":50346852,"strand":-1,"description":"zinc finger MYND-type containing 10 [Source:HGNC Symbol;Acc:HGNC:19412]"}, {"versioned_ensembl_gene_id":"ENSG00000267523.1","gene_symbol":"AC008735.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55661901,"end":55674715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237701.1","gene_symbol":"ATP5JP1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359997","summary":null,"start":6900753,"end":6901372,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23933]"}, {"versioned_ensembl_gene_id":"ENSG00000280767.3","gene_symbol":"AL732314.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":419157,"end":421980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119927.13","gene_symbol":"GPAM","gene_name":"glycerol-3-phosphate acyltransferase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:24865]","synonyms":"KIAA1560,GPAT1,MGC26846","biotype":"protein_coding","ncbi_id":"57678","summary":"This gene encodes a mitochondrial enzyme which prefers saturated fatty acids as its substrate for the synthesis of glycerolipids. This metabolic pathway's first step is catalyzed by the encoded enzyme. Two forms for this enzyme exist, one in the mitochondria and one in the endoplasmic reticulum. Two alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]","start":112149864,"end":112215377,"strand":-1,"description":"glycerol-3-phosphate acyltransferase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:24865]"}, {"versioned_ensembl_gene_id":"ENSG00000196562.14","gene_symbol":"SULF2","gene_name":"sulfatase 2 [Source:HGNC Symbol;Acc:HGNC:20392]","synonyms":"SULF-2,KIAA1247,HSULF-2","biotype":"protein_coding","ncbi_id":"55959","summary":"Heparan sulfate proteoglycans (HSPGs) act as coreceptors for numerous heparin-binding growth factors and cytokines and are involved in cell signaling. Heparan sulfate 6-O-endosulfatases, such as SULF2, selectively remove 6-O-sulfate groups from heparan sulfate. This activity modulates the effects of heparan sulfate by altering binding sites for signaling molecules (Dai et al., 2005 [PubMed 16192265]).[supplied by OMIM, Mar 2008]","start":47656348,"end":47786616,"strand":-1,"description":"sulfatase 2 [Source:HGNC Symbol;Acc:HGNC:20392]"}, {"versioned_ensembl_gene_id":"ENSG00000280994.1","gene_symbol":"LINC01347","gene_name":"long intergenic non-protein coding RNA 1347 [Source:NCBI gene;Acc:731275]","synonyms":null,"biotype":"lincRNA","ncbi_id":"731275","summary":null,"start":243056307,"end":243101744,"strand":-1,"description":"long intergenic non-protein coding RNA 1347 [Source:NCBI gene;Acc:731275]"}, {"versioned_ensembl_gene_id":"ENSG00000204574.12","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"EST123147,ABC50","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30571376,"end":30597179,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000249407.1","gene_symbol":"IL20RB-AS1","gene_name":"IL20RB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40298]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107986136","summary":null,"start":136959125,"end":136982196,"strand":-1,"description":"IL20RB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40298]"}, {"versioned_ensembl_gene_id":"ENSG00000237013.1","gene_symbol":"LINC01812","gene_name":"long intergenic non-protein coding RNA 1812 [Source:HGNC Symbol;Acc:HGNC:52616]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927701","summary":null,"start":67796054,"end":67825562,"strand":-1,"description":"long intergenic non-protein coding RNA 1812 [Source:HGNC Symbol;Acc:HGNC:52616]"}, {"versioned_ensembl_gene_id":"ENSG00000166669.13","gene_symbol":"ATF7IP2","gene_name":"activating transcription factor 7 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:20397]","synonyms":"FLJ12668","biotype":"protein_coding","ncbi_id":"80063","summary":null,"start":10326434,"end":10483638,"strand":1,"description":"activating transcription factor 7 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:20397]"}, {"versioned_ensembl_gene_id":"ENSG00000235074.1","gene_symbol":"CR788250.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32591998,"end":32592093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282176.1","gene_symbol":"FLJ13224","gene_name":"uncharacterized LOC79857 [Source:NCBI gene;Acc:79857]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"79857","summary":null,"start":31326589,"end":31328102,"strand":1,"description":"uncharacterized LOC79857 [Source:NCBI gene;Acc:79857]"}, {"versioned_ensembl_gene_id":"ENSG00000126107.14","gene_symbol":"HECTD3","gene_name":"HECT domain E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:26117]","synonyms":"FLJ21156","biotype":"protein_coding","ncbi_id":"79654","summary":"The protein encoded by this gene transfers ubiquitin from an E2 ubiquitin-conjugating enzyme to targeted substrates, leading to the degradation of those substrates. The encoded protein has been shown to transfer ubiquitin to TRIOBP to facilitate cell cycle progression, and to STX8. [provided by RefSeq, Dec 2012]","start":45002540,"end":45011329,"strand":-1,"description":"HECT domain E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:26117]"}, {"versioned_ensembl_gene_id":"ENSG00000140538.16","gene_symbol":"NTRK3","gene_name":"neurotrophic receptor tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:8033]","synonyms":"TRKC","biotype":"protein_coding","ncbi_id":"4916","summary":"This gene encodes a member of the neurotrophic tyrosine receptor kinase (NTRK) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. Signalling through this kinase leads to cell differentiation and may play a role in the development of proprioceptive neurons that sense body position. Mutations in this gene have been associated with medulloblastomas, secretory breast carcinomas and other cancers. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":87859751,"end":88256768,"strand":-1,"description":"neurotrophic receptor tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:8033]"}, {"versioned_ensembl_gene_id":"ENSG00000232787.1","gene_symbol":"OR7L1P","gene_name":"olfactory receptor family 7 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14827]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"79499","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131596139,"end":131596838,"strand":1,"description":"olfactory receptor family 7 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14827]"}, {"versioned_ensembl_gene_id":"ENSG00000227645.2","gene_symbol":"RPL7P54","gene_name":"ribosomal protein L7 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271146","summary":null,"start":78763226,"end":78763899,"strand":1,"description":"ribosomal protein L7 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36817]"}, {"versioned_ensembl_gene_id":"ENSG00000176029.13","gene_symbol":"C11orf16","gene_name":"chromosome 11 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:1169]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56673","summary":null,"start":8920076,"end":8933006,"strand":-1,"description":"chromosome 11 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:1169]"}, {"versioned_ensembl_gene_id":"ENSG00000143545.8","gene_symbol":"RAB13","gene_name":"RAB13, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9762]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5872","summary":"This gene is a member of the Rab family of small G proteins and plays a role in regulating membrane trafficking between trans-Golgi network (TGN) and recycling endosomes (RE). The encoded protein is involved in the assembly of tight junctions, which are components of the apical junctional complex (AJC) of epithelial cells. The AJC plays a role in forming a barrier between luminal contents and the underlying tissue. Additional functions associated with the protein include endocytic recycling of occludin, regulation of epithelial cell scattering, neuronal regeneration and regulation of neurite outgrowth. Alternately spliced transcript variants have been observed for this gene. A pseudogene associated with this gene is located on chromosome 12. [provided by RefSeq, Jan 2013]","start":153981617,"end":153986358,"strand":-1,"description":"RAB13, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9762]"}, {"versioned_ensembl_gene_id":"ENSG00000105518.13","gene_symbol":"TMEM205","gene_name":"transmembrane protein 205 [Source:HGNC Symbol;Acc:HGNC:29631]","synonyms":"UNQ501,MBC3205","biotype":"protein_coding","ncbi_id":"374882","summary":null,"start":11342776,"end":11346518,"strand":-1,"description":"transmembrane protein 205 [Source:HGNC Symbol;Acc:HGNC:29631]"}, {"versioned_ensembl_gene_id":"ENSG00000267174.5","gene_symbol":"AC011472.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":11300777,"end":11324441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276625.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"cl-42,CD158A,47.11,p58.1,nkat1","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769794,"end":54784109,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000258314.3","gene_symbol":"AL589182.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19024090,"end":19055551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126254.11","gene_symbol":"RBM42","gene_name":"RNA binding motif protein 42 [Source:HGNC Symbol;Acc:HGNC:28117]","synonyms":"MGC10433","biotype":"protein_coding","ncbi_id":"79171","summary":null,"start":35629030,"end":35637686,"strand":1,"description":"RNA binding motif protein 42 [Source:HGNC Symbol;Acc:HGNC:28117]"}, {"versioned_ensembl_gene_id":"ENSG00000236018.2","gene_symbol":"AC004898.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157197600,"end":157198511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212126.3","gene_symbol":"TAS2R50","gene_name":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]","synonyms":"T2R51","biotype":"protein_coding","ncbi_id":"259296","summary":"TAS2R50 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). See also TAS2R10 (MIM 604791).[supplied by OMIM, Mar 2008]","start":10985913,"end":10986912,"strand":-1,"description":"taste 2 receptor member 50 [Source:HGNC Symbol;Acc:HGNC:18882]"}, {"versioned_ensembl_gene_id":"ENSG00000256651.1","gene_symbol":"AC006518.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10831074,"end":10832016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227534.1","gene_symbol":"Z83841.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65469087,"end":65470380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230643.1","gene_symbol":"AP000533.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15588361,"end":15588478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243969.1","gene_symbol":"AC073359.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154827016,"end":154861017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271159.1","gene_symbol":"HINT1P2","gene_name":"histidine triad nucleotide binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38049]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100233146","summary":null,"start":95018163,"end":95018397,"strand":-1,"description":"histidine triad nucleotide binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38049]"}, {"versioned_ensembl_gene_id":"ENSG00000010017.12","gene_symbol":"RANBP9","gene_name":"RAN binding protein 9 [Source:HGNC Symbol;Acc:HGNC:13727]","synonyms":"RanBPM","biotype":"protein_coding","ncbi_id":"10048","summary":"This gene encodes a protein that binds RAN, a small GTP binding protein belonging to the RAS superfamily that is essential for the translocation of RNA and proteins through the nuclear pore complex. The protein encoded by this gene has also been shown to interact with several other proteins, including met proto-oncogene, homeodomain interacting protein kinase 2, androgen receptor, and cyclin-dependent kinase 11. [provided by RefSeq, Jul 2008]","start":13621498,"end":13711564,"strand":-1,"description":"RAN binding protein 9 [Source:HGNC Symbol;Acc:HGNC:13727]"}, {"versioned_ensembl_gene_id":"ENSG00000274010.1","gene_symbol":"AC006011.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127840606,"end":127841763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185261.14","gene_symbol":"KIAA0825","gene_name":"KIAA0825 [Source:HGNC Symbol;Acc:HGNC:28532]","synonyms":"DKFZp686F0372,C5orf36,MGC34713","biotype":"protein_coding","ncbi_id":"285600","summary":null,"start":94152966,"end":94618597,"strand":-1,"description":"KIAA0825 [Source:HGNC Symbol;Acc:HGNC:28532]"}, {"versioned_ensembl_gene_id":"ENSG00000283132.1","gene_symbol":"AC006453.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89622213,"end":89640635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281962.1","gene_symbol":"IGHV3-23","gene_name":"immunoglobulin heavy variable 3-23 [Source:HGNC Symbol;Acc:HGNC:5588]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28442","summary":"IGHV3-23 belongs to a cluster of approximately 40 functional variable (V) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the V gene cluster, see (MIM 147070).[supplied by OMIM, Apr 2008]","start":106269377,"end":106269911,"strand":-1,"description":"immunoglobulin heavy variable 3-23 [Source:HGNC Symbol;Acc:HGNC:5588]"}, {"versioned_ensembl_gene_id":"ENSG00000228024.1","gene_symbol":"CYP1D1P","gene_name":"cytochrome P450 family 1 subfamily D member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39968]","synonyms":"CYP1A8P","biotype":"unprocessed_pseudogene","ncbi_id":"100133307","summary":null,"start":73042745,"end":73056528,"strand":1,"description":"cytochrome P450 family 1 subfamily D member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39968]"}, {"versioned_ensembl_gene_id":"ENSG00000267986.1","gene_symbol":"AC130469.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8581160,"end":8582715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231169.4","gene_symbol":"EEF1B2P1","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3207]","synonyms":"EEF1B1","biotype":"processed_pseudogene","ncbi_id":"1932","summary":null,"start":52505191,"end":52505862,"strand":1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3207]"}, {"versioned_ensembl_gene_id":"ENSG00000181260.8","gene_symbol":"MTHFD2P7","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48865]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442098","summary":null,"start":179464346,"end":179465328,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48865]"}, {"versioned_ensembl_gene_id":"ENSG00000204815.9","gene_symbol":"TTC25","gene_name":"tetratricopeptide repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:25280]","synonyms":"DKFZP434H0115","biotype":"protein_coding","ncbi_id":"83538","summary":"This gene encodes a tetratricopeptide repeat domain-containing protein that localizes to ciliary axonmenes and plays a role in the docking of the outer dynein arm to cilia. Mutations in this gene cause severely reduced ciliary motility and the disorder CILD35 (ciliary dyskinesia,primary, 35). Primary ciliary dyskinesia is often associated with recurrent respiratory infections, immotile spermatozoa, and situs inversus; an inversion in left-right body symmetry. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]","start":41930635,"end":41965651,"strand":1,"description":"tetratricopeptide repeat domain 25 [Source:HGNC Symbol;Acc:HGNC:25280]"}, {"versioned_ensembl_gene_id":"ENSG00000234243.7","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"C6orf9,G18.1a,G18.2,AGS4,G18,G18.1b,NG1","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32267189,"end":32271946,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000259409.1","gene_symbol":"AC021755.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40088832,"end":40089386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254634.4","gene_symbol":"SMG1P6","gene_name":"SMG1P6, nonsense mediated mRNA decay associated PI3K related kinasepseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49863]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422558","summary":null,"start":29425800,"end":29447026,"strand":-1,"description":"SMG1P6, nonsense mediated mRNA decay associated PI3K related kinasepseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49863]"}, {"versioned_ensembl_gene_id":"ENSG00000258757.1","gene_symbol":"AL133453.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52640839,"end":52641566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251576.1","gene_symbol":"LINC01267","gene_name":"long intergenic non-protein coding RNA 1267 [Source:HGNC Symbol;Acc:HGNC:50320]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927565","summary":null,"start":14348451,"end":14352568,"strand":-1,"description":"long intergenic non-protein coding RNA 1267 [Source:HGNC Symbol;Acc:HGNC:50320]"}, {"versioned_ensembl_gene_id":"ENSG00000173926.5","gene_symbol":"MARCH3","gene_name":"membrane associated ring-CH-type finger 3 [Source:HGNC Symbol;Acc:HGNC:28728]","synonyms":"RNF173,MGC48332,MARCH-III","biotype":"protein_coding","ncbi_id":"115123","summary":"This gene encodes a member of the membrane-associated RING-CH (MARCH) family. The encoded protein is an E3 ubiquitin-protein ligase that may be involved in regulation of the endosomal transport pathway. [provided by RefSeq, Mar 2013]","start":126867714,"end":127030808,"strand":-1,"description":"membrane associated ring-CH-type finger 3 [Source:HGNC Symbol;Acc:HGNC:28728]"}, {"versioned_ensembl_gene_id":"ENSG00000237938.5","gene_symbol":"AL450998.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15720312,"end":15736896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253428.1","gene_symbol":"LINC01942","gene_name":"long intergenic non-protein coding RNA 1942 [Source:HGNC Symbol;Acc:HGNC:52766]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377736","summary":null,"start":173689459,"end":173705849,"strand":1,"description":"long intergenic non-protein coding RNA 1942 [Source:HGNC Symbol;Acc:HGNC:52766]"}, {"versioned_ensembl_gene_id":"ENSG00000173809.17","gene_symbol":"TDRD12","gene_name":"tudor domain containing 12 [Source:HGNC Symbol;Acc:HGNC:25044]","synonyms":"FLJ13072,ECAT8","biotype":"protein_coding","ncbi_id":"91646","summary":null,"start":32719753,"end":32829580,"strand":1,"description":"tudor domain containing 12 [Source:HGNC Symbol;Acc:HGNC:25044]"}, {"versioned_ensembl_gene_id":"ENSG00000105726.16","gene_symbol":"ATP13A1","gene_name":"ATPase 13A1 [Source:HGNC Symbol;Acc:HGNC:24215]","synonyms":"KIAA1825,FLJ31858,CGI-152,ATP13A","biotype":"protein_coding","ncbi_id":"57130","summary":null,"start":19645198,"end":19663693,"strand":-1,"description":"ATPase 13A1 [Source:HGNC Symbol;Acc:HGNC:24215]"}, {"versioned_ensembl_gene_id":"ENSG00000236724.1","gene_symbol":"AL137071.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3875584,"end":3878809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267838.2","gene_symbol":"AC245884.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54438665,"end":54439544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249982.1","gene_symbol":"AC005823.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51332679,"end":51334090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256254.1","gene_symbol":"AP000619.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102766801,"end":102767927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242685.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32877327,"end":32899448,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000230141.11","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-D0-alpha,HLA-DZA,HLA-DNA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":33037640,"end":33043074,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000230381.2","gene_symbol":"AL136376.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116429049,"end":116433368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233154.5","gene_symbol":"LINC01762","gene_name":"long intergenic non-protein coding RNA 1762 [Source:HGNC Symbol;Acc:HGNC:52552]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929023","summary":null,"start":116423724,"end":116478842,"strand":-1,"description":"long intergenic non-protein coding RNA 1762 [Source:HGNC Symbol;Acc:HGNC:52552]"}, {"versioned_ensembl_gene_id":"ENSG00000169181.12","gene_symbol":"GSG1L","gene_name":"GSG1 like [Source:HGNC Symbol;Acc:HGNC:28283]","synonyms":"KTSR5831,PRO19651,MGC18079","biotype":"protein_coding","ncbi_id":"146395","summary":null,"start":27787535,"end":28063509,"strand":-1,"description":"GSG1 like [Source:HGNC Symbol;Acc:HGNC:28283]"}, {"versioned_ensembl_gene_id":"ENSG00000183072.9","gene_symbol":"NKX2-5","gene_name":"NK2 homeobox 5 [Source:HGNC Symbol;Acc:HGNC:2488]","synonyms":"CSX1,CSX,NKX4-1,NKX2E,NKX2.5","biotype":"protein_coding","ncbi_id":"1482","summary":"This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":173232109,"end":173235357,"strand":-1,"description":"NK2 homeobox 5 [Source:HGNC Symbol;Acc:HGNC:2488]"}, {"versioned_ensembl_gene_id":"ENSG00000197451.11","gene_symbol":"HNRNPAB","gene_name":"heterogeneous nuclear ribonucleoprotein A/B [Source:HGNC Symbol;Acc:HGNC:5034]","synonyms":"HNRPAB,FLJ40338,ABBP1","biotype":"protein_coding","ncbi_id":"3182","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are produced by RNA polymerase II and are components of the heterogeneous nuclear RNA (hnRNA) complexes. They are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene, which binds to one of the components of the multiprotein editosome complex, has two repeats of quasi-RRM (RNA recognition motif) domains that bind to RNAs. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":178204507,"end":178211163,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A/B [Source:HGNC Symbol;Acc:HGNC:5034]"}, {"versioned_ensembl_gene_id":"ENSG00000268230.5","gene_symbol":"AC012313.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":58346854,"end":58362751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249616.1","gene_symbol":"CCNB3P1","gene_name":"cyclin B3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50851]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131678","summary":null,"start":26739753,"end":26741183,"strand":-1,"description":"cyclin B3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50851]"}, {"versioned_ensembl_gene_id":"ENSG00000228656.1","gene_symbol":"MYO5BP3","gene_name":"myosin VB pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38497]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441442","summary":null,"start":63761546,"end":63762824,"strand":-1,"description":"myosin VB pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38497]"}, {"versioned_ensembl_gene_id":"ENSG00000250703.1","gene_symbol":"AC113347.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26670334,"end":26670481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224267.1","gene_symbol":"AL772155.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63728877,"end":63744910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279611.1","gene_symbol":"AC012313.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58350795,"end":58351720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249099.1","gene_symbol":"AC025475.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26382519,"end":26399819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235084.3","gene_symbol":"CHCHD2P6","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39590]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645317","summary":null,"start":15604597,"end":15605043,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39590]"}, {"versioned_ensembl_gene_id":"ENSG00000121410.11","gene_symbol":"A1BG","gene_name":"alpha-1-B glycoprotein [Source:HGNC Symbol;Acc:HGNC:5]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1","summary":"The protein encoded by this gene is a plasma glycoprotein of unknown function. The protein shows sequence similarity to the variable regions of some immunoglobulin supergene family member proteins. [provided by RefSeq, Jul 2008]","start":58345178,"end":58353499,"strand":-1,"description":"alpha-1-B glycoprotein [Source:HGNC Symbol;Acc:HGNC:5]"}, {"versioned_ensembl_gene_id":"ENSG00000170775.2","gene_symbol":"GPR37","gene_name":"G protein-coupled receptor 37 [Source:HGNC Symbol;Acc:HGNC:4494]","synonyms":"PAELR,hET(B)R-LP,EDNRBL","biotype":"protein_coding","ncbi_id":"2861","summary":"This gene is a member of the G protein-coupled receptor family. The encoded protein contains seven transmembrane domains and is found in cell and endoplasmic reticulum membranes. G protein-coupled receptors are involved in translating outside signals into G protein mediated intracellular effects. This gene product interacts with Parkin and is involved in juvenile Parkinson disease. [provided by RefSeq, Oct 2012]","start":124745997,"end":124765627,"strand":-1,"description":"G protein-coupled receptor 37 [Source:HGNC Symbol;Acc:HGNC:4494]"}, {"versioned_ensembl_gene_id":"ENSG00000102393.9","gene_symbol":"GLA","gene_name":"galactosidase alpha [Source:HGNC Symbol;Acc:HGNC:4296]","synonyms":"GALA","biotype":"protein_coding","ncbi_id":"2717","summary":"This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq, Jul 2008]","start":101397803,"end":101407925,"strand":-1,"description":"galactosidase alpha [Source:HGNC Symbol;Acc:HGNC:4296]"}, {"versioned_ensembl_gene_id":"ENSG00000188916.8","gene_symbol":"FAM196A","gene_name":"family with sequence similarity 196 member A [Source:HGNC Symbol;Acc:HGNC:33859]","synonyms":"INSYN2,FLJ45557,C10orf141","biotype":"protein_coding","ncbi_id":"642938","summary":null,"start":127135426,"end":127196158,"strand":-1,"description":"family with sequence similarity 196 member A [Source:HGNC Symbol;Acc:HGNC:33859]"}, {"versioned_ensembl_gene_id":"ENSG00000260729.1","gene_symbol":"AC009690.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":72284727,"end":72375981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268496.1","gene_symbol":"AC245884.9","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":54434183,"end":54434665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281655.1","gene_symbol":"AP000851.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102681310,"end":102683913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253741.1","gene_symbol":"AC108002.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142702252,"end":142726973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274378.1","gene_symbol":"AC005702.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60025859,"end":60030746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205867.3","gene_symbol":"KRTAP5-2","gene_name":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]","synonyms":"KRTAP5.2,KRTAP5-8","biotype":"protein_coding","ncbi_id":"440021","summary":null,"start":1597177,"end":1598294,"strand":-1,"description":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]"}, {"versioned_ensembl_gene_id":"ENSG00000143643.12","gene_symbol":"TTC13","gene_name":"tetratricopeptide repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:26204]","synonyms":"FLJ22584","biotype":"protein_coding","ncbi_id":"79573","summary":null,"start":230906243,"end":230978875,"strand":-1,"description":"tetratricopeptide repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:26204]"}, {"versioned_ensembl_gene_id":"ENSG00000069974.15","gene_symbol":"RAB27A","gene_name":"RAB27A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9766]","synonyms":"HsT18676,GS2,RAM,RAB27","biotype":"protein_coding","ncbi_id":"5873","summary":"The protein encoded by this gene belongs to the small GTPase superfamily, Rab family. The protein is membrane-bound and may be involved in protein transport and small GTPase mediated signal transduction. Mutations in this gene are associated with Griscelli syndrome type 2. Alternative splicing occurs at this locus and four transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":55202966,"end":55319113,"strand":-1,"description":"RAB27A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9766]"}, {"versioned_ensembl_gene_id":"ENSG00000165555.9","gene_symbol":"NOXRED1","gene_name":"NADP dependent oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20487]","synonyms":"FLJ32809,C14orf148","biotype":"protein_coding","ncbi_id":"122945","summary":null,"start":77394021,"end":77423517,"strand":-1,"description":"NADP dependent oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20487]"}, {"versioned_ensembl_gene_id":"ENSG00000178852.15","gene_symbol":"EFCAB13","gene_name":"EF-hand calcium binding domain 13 [Source:HGNC Symbol;Acc:HGNC:26864]","synonyms":"FLJ40342,C17orf57","biotype":"protein_coding","ncbi_id":"124989","summary":null,"start":47323290,"end":47441312,"strand":1,"description":"EF-hand calcium binding domain 13 [Source:HGNC Symbol;Acc:HGNC:26864]"}, {"versioned_ensembl_gene_id":"ENSG00000155189.11","gene_symbol":"AGPAT5","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:20886]","synonyms":"LPAAT-epsilon,LPAAT-e,FLJ11210","biotype":"protein_coding","ncbi_id":"55326","summary":"This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. This integral membrane protein converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. A pseudogene of this gene is present on the Y chromosome. [provided by RefSeq, Aug 2014]","start":6708357,"end":6759666,"strand":1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:20886]"}, {"versioned_ensembl_gene_id":"ENSG00000234183.1","gene_symbol":"LINC01952","gene_name":"long intergenic non-protein coding RNA 1952 [Source:HGNC Symbol;Acc:HGNC:52775]","synonyms":"AC004854.4","biotype":"antisense_RNA","ncbi_id":"105375261","summary":null,"start":44848416,"end":44849568,"strand":1,"description":"long intergenic non-protein coding RNA 1952 [Source:HGNC Symbol;Acc:HGNC:52775]"}, {"versioned_ensembl_gene_id":"ENSG00000120262.9","gene_symbol":"CCDC170","gene_name":"coiled-coil domain containing 170 [Source:HGNC Symbol;Acc:HGNC:21177]","synonyms":"FLJ23305,C6orf97,bA282P11.1","biotype":"protein_coding","ncbi_id":"80129","summary":"The function of this gene and its encoded protein is not known. Several genome-wide association studies have implicated the region around this gene to be involved in breast cancer and bone mineral density, but no link to this specific gene has been found. [provided by RefSeq, May 2010]","start":151494030,"end":151621193,"strand":1,"description":"coiled-coil domain containing 170 [Source:HGNC Symbol;Acc:HGNC:21177]"}, {"versioned_ensembl_gene_id":"ENSG00000258510.2","gene_symbol":"AC007954.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77359423,"end":77359916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100583.4","gene_symbol":"SAMD15","gene_name":"sterile alpha motif domain containing 15 [Source:HGNC Symbol;Acc:HGNC:18631]","synonyms":"FLJ35963,FAM15A,C14orf174","biotype":"protein_coding","ncbi_id":"161394","summary":null,"start":77376689,"end":77391497,"strand":1,"description":"sterile alpha motif domain containing 15 [Source:HGNC Symbol;Acc:HGNC:18631]"}, {"versioned_ensembl_gene_id":"ENSG00000231641.9","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30262891,"end":30291774,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000084207.15","gene_symbol":"GSTP1","gene_name":"glutathione S-transferase pi 1 [Source:HGNC Symbol;Acc:HGNC:4638]","synonyms":"GSTP,GST3,FAEES3","biotype":"protein_coding","ncbi_id":"2950","summary":"Glutathione S-transferases (GSTs) are a family of enzymes that play an important role in detoxification by catalyzing the conjugation of many hydrophobic and electrophilic compounds with reduced glutathione. Based on their biochemical, immunologic, and structural properties, the soluble GSTs are categorized into 4 main classes: alpha, mu, pi, and theta. This GST family member is a polymorphic gene encoding active, functionally different GSTP1 variant proteins that are thought to function in xenobiotic metabolism and play a role in susceptibility to cancer, and other diseases. [provided by RefSeq, Jul 2008]","start":67583595,"end":67586660,"strand":1,"description":"glutathione S-transferase pi 1 [Source:HGNC Symbol;Acc:HGNC:4638]"}, {"versioned_ensembl_gene_id":"ENSG00000135074.15","gene_symbol":"ADAM19","gene_name":"ADAM metallopeptidase domain 19 [Source:HGNC Symbol;Acc:HGNC:197]","synonyms":"MLTNB","biotype":"protein_coding","ncbi_id":"8728","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This member is a type I transmembrane protein and serves as a marker for dendritic cell differentiation. It has been demonstrated to be an active metalloproteinase, which may be involved in normal physiological processes such as cell migration, cell adhesion, cell-cell and cell-matrix interactions, and signal transduction. It is proposed to play a role in pathological processes, such as cancer, inflammatory diseases, renal diseases, and Alzheimer's disease. [provided by RefSeq, May 2013]","start":157395534,"end":157575775,"strand":-1,"description":"ADAM metallopeptidase domain 19 [Source:HGNC Symbol;Acc:HGNC:197]"}, {"versioned_ensembl_gene_id":"ENSG00000103876.11","gene_symbol":"FAH","gene_name":"fumarylacetoacetate hydrolase [Source:HGNC Symbol;Acc:HGNC:3579]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2184","summary":"This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT). [provided by RefSeq, Jul 2008]","start":80152490,"end":80186946,"strand":1,"description":"fumarylacetoacetate hydrolase [Source:HGNC Symbol;Acc:HGNC:3579]"}, {"versioned_ensembl_gene_id":"ENSG00000239482.6","gene_symbol":"AC112487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112302478,"end":112332791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172548.14","gene_symbol":"NIPAL4","gene_name":"NIPA like domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28018]","synonyms":"ICHYN","biotype":"protein_coding","ncbi_id":"348938","summary":"This gene likely encodes a membrane receptor. Mutations in this gene have been associated with autosomal recessive congenital ichthyosis. [provided by RefSeq, Feb 2010]","start":157460019,"end":157474717,"strand":1,"description":"NIPA like domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28018]"}, {"versioned_ensembl_gene_id":"ENSG00000237962.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":30974428,"end":30980608,"strand":1,"description":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]"}, {"versioned_ensembl_gene_id":"ENSG00000230647.1","gene_symbol":"AC022816.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14374139,"end":14421026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230025.1","gene_symbol":"AC007967.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8971751,"end":8974095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081870.11","gene_symbol":"HSPB11","gene_name":"heat shock protein family B (small) member 11 [Source:HGNC Symbol;Acc:HGNC:25019]","synonyms":"PP25,IFT25,HSPCO34,C1orf41","biotype":"protein_coding","ncbi_id":"51668","summary":null,"start":53916574,"end":53945929,"strand":-1,"description":"heat shock protein family B (small) member 11 [Source:HGNC Symbol;Acc:HGNC:25019]"}, {"versioned_ensembl_gene_id":"ENSG00000249853.7","gene_symbol":"HS3ST5","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 5 [Source:HGNC Symbol;Acc:HGNC:19419]","synonyms":"3-OST-5","biotype":"protein_coding","ncbi_id":"222537","summary":"HS3ST5 belongs to a group of heparan sulfate 3-O-sulfotransferases (EC 2.8.2.23) that transfer sulfate from 3-prime-phosphoadenosine 5-prime phosphosulfate (PAPS) to heparan sulfate and heparin (Mochizuki et al., 2003 [PubMed 12740361]).[supplied by OMIM, Mar 2008]","start":114055586,"end":114343045,"strand":-1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 5 [Source:HGNC Symbol;Acc:HGNC:19419]"}, {"versioned_ensembl_gene_id":"ENSG00000255339.6","gene_symbol":"AL133352.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":100505628,"end":100529881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250101.1","gene_symbol":"AC106795.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177939622,"end":177983054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236530.2","gene_symbol":"KPNA2P1","gene_name":"karyopherin subunit alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52871]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643513","summary":null,"start":80079532,"end":80081122,"strand":1,"description":"karyopherin subunit alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52871]"}, {"versioned_ensembl_gene_id":"ENSG00000235145.2","gene_symbol":"RPSAP16","gene_name":"ribosomal protein SA pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35478]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270872","summary":null,"start":179968686,"end":179969506,"strand":1,"description":"ribosomal protein SA pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35478]"}, {"versioned_ensembl_gene_id":"ENSG00000219395.2","gene_symbol":"HSPA8P15","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:44930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420051","summary":null,"start":151411259,"end":151413945,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:44930]"}, {"versioned_ensembl_gene_id":"ENSG00000063438.16","gene_symbol":"AHRR","gene_name":"aryl-hydrocarbon receptor repressor [Source:HGNC Symbol;Acc:HGNC:346]","synonyms":"KIAA1234,bHLHe77,AHHR,AHH","biotype":"protein_coding","ncbi_id":"57491","summary":"The protein encoded by this gene participates in the aryl hydrocarbon receptor (AhR) signaling cascade, which mediates dioxin toxicity, and is involved in regulation of cell growth and differentiation. It functions as a feedback modulator by repressing AhR-dependent gene expression. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2011]","start":304176,"end":438291,"strand":1,"description":"aryl-hydrocarbon receptor repressor [Source:HGNC Symbol;Acc:HGNC:346]"}, {"versioned_ensembl_gene_id":"ENSG00000278129.1","gene_symbol":"ZNF8","gene_name":"zinc finger protein 8 [Source:HGNC Symbol;Acc:HGNC:13154]","synonyms":"Zfp128,HF.18","biotype":"protein_coding","ncbi_id":"7554","summary":null,"start":58278951,"end":58302805,"strand":1,"description":"zinc finger protein 8 [Source:HGNC Symbol;Acc:HGNC:13154]"}, {"versioned_ensembl_gene_id":"ENSG00000214278.4","gene_symbol":"AC010442.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":403731,"end":404546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248943.1","gene_symbol":"AC140125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177801204,"end":177803344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145782.12","gene_symbol":"ATG12","gene_name":"autophagy related 12 [Source:HGNC Symbol;Acc:HGNC:588]","synonyms":"APG12L,APG12","biotype":"protein_coding","ncbi_id":"9140","summary":"Autophagy is a process of bulk protein degradation in which cytoplasmic components, including organelles, are enclosed in double-membrane structures called autophagosomes and delivered to lysosomes or vacuoles for degradation. ATG12 is the human homolog of a yeast protein involved in autophagy (Mizushima et al., 1998 [PubMed 9852036]).[supplied by OMIM, Mar 2008]","start":115828200,"end":115841858,"strand":-1,"description":"autophagy related 12 [Source:HGNC Symbol;Acc:HGNC:588]"}, {"versioned_ensembl_gene_id":"ENSG00000148634.15","gene_symbol":"HERC4","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:24521]","synonyms":"KIAA1593,DKFZP564G092","biotype":"protein_coding","ncbi_id":"26091","summary":"HERC4 belongs to the HERC family of ubiquitin ligases, all of which contain a HECT domain and at least 1 RCC1 (MIM 179710)-like domain (RLD). The 350-amino acid HECT domain is predicted to catalyze the formation of a thioester with ubiquitin before transferring it to a substrate, and the RLD is predicted to act as a guanine nucleotide exchange factor for small G proteins (Hochrainer et al., 2005 [PubMed 15676274]).[supplied by OMIM, Mar 2008]","start":67921899,"end":68075348,"strand":-1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:24521]"}, {"versioned_ensembl_gene_id":"ENSG00000259448.2","gene_symbol":"LINC02352","gene_name":"long intergenic non-protein coding RNA 2352 [Source:HGNC Symbol;Acc:HGNC:53274]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102725022","summary":null,"start":31216020,"end":31224445,"strand":1,"description":"long intergenic non-protein coding RNA 2352 [Source:HGNC Symbol;Acc:HGNC:53274]"}, {"versioned_ensembl_gene_id":"ENSG00000259772.6","gene_symbol":"AC012236.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31221999,"end":31230838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280416.1","gene_symbol":"AC009084.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":66944660,"end":66945096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214263.2","gene_symbol":"RPSAP53","gene_name":"ribosomal protein SA pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36641]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400141","summary":null,"start":67266845,"end":67267706,"strand":-1,"description":"ribosomal protein SA pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36641]"}, {"versioned_ensembl_gene_id":"ENSG00000237797.1","gene_symbol":"AL161935.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31693084,"end":31707388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000025800.13","gene_symbol":"KPNA6","gene_name":"karyopherin subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:6399]","synonyms":"MGC17918,KPNA7,IPOA7,FLJ11249","biotype":"protein_coding","ncbi_id":"23633","summary":"Nucleocytoplasmic transport, a signal- and energy-dependent process, takes place through nuclear pore complexes embedded in the nuclear envelope. The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor, a heterodimer of importin alpha and beta subunits also known as karyopherins. Importin alpha binds the NLS-containing cargo in the cytoplasm and importin beta docks the complex at the cytoplasmic side of the nuclear pore complex. In the presence of nucleoside triphosphates and the small GTP binding protein Ran, the complex moves into the nuclear pore complex and the importin subunits dissociate. Importin alpha enters the nucleoplasm with its passenger protein and importin beta remains at the pore. The protein encoded by this gene is a member of the importin alpha family. [provided by RefSeq, Jul 2008]","start":32108038,"end":32176568,"strand":1,"description":"karyopherin subunit alpha 6 [Source:HGNC Symbol;Acc:HGNC:6399]"}, {"versioned_ensembl_gene_id":"ENSG00000225684.3","gene_symbol":"FAM225B","gene_name":"family with sequence similarity 225 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21865]","synonyms":"NCRNA00256B,LINC00256B,C9orf110","biotype":"lincRNA","ncbi_id":"100128385","summary":null,"start":113103338,"end":113111500,"strand":-1,"description":"family with sequence similarity 225 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21865]"}, {"versioned_ensembl_gene_id":"ENSG00000254991.1","gene_symbol":"AC124276.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12066929,"end":12073014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223834.2","gene_symbol":"AL161935.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31604600,"end":31606218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254829.1","gene_symbol":"AP003032.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78015715,"end":78016495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185821.3","gene_symbol":"OR6C76","gene_name":"olfactory receptor family 6 subfamily C member 76 [Source:HGNC Symbol;Acc:HGNC:31305]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390326","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55426254,"end":55427192,"strand":1,"description":"olfactory receptor family 6 subfamily C member 76 [Source:HGNC Symbol;Acc:HGNC:31305]"}, {"versioned_ensembl_gene_id":"ENSG00000224602.1","gene_symbol":"RPS26P5","gene_name":"ribosomal protein S26 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387495","summary":null,"start":16121310,"end":16121644,"strand":-1,"description":"ribosomal protein S26 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23776]"}, {"versioned_ensembl_gene_id":"ENSG00000254675.1","gene_symbol":"AP003032.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78022933,"end":78023721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250346.1","gene_symbol":"EEF1GP2","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130260","summary":null,"start":147922179,"end":147923421,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44557]"}, {"versioned_ensembl_gene_id":"ENSG00000148985.19","gene_symbol":"PGAP2","gene_name":"post-GPI attachment to proteins 2 [Source:HGNC Symbol;Acc:HGNC:17893]","synonyms":"CWH43-N,MRT21,FRAG1","biotype":"protein_coding","ncbi_id":"27315","summary":"The protein encoded by this gene plays a role in the maturation of glycosylphosphatidylinositol (GPI) anchors on GPI-anchored proteins. Mutations in this gene are associated with an autosomal recessive syndrome characterized by hyperphosphatasia and intellectual disability. [provided by RefSeq, Jul 2017]","start":3797724,"end":3826371,"strand":1,"description":"post-GPI attachment to proteins 2 [Source:HGNC Symbol;Acc:HGNC:17893]"}, {"versioned_ensembl_gene_id":"ENSG00000260657.2","gene_symbol":"AC107871.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68267792,"end":68277994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231542.1","gene_symbol":"TAB3-AS1","gene_name":"TAB3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20176]","synonyms":"OTTHUMG00000021331,CXorf29","biotype":"antisense_RNA","ncbi_id":"727682","summary":null,"start":30834623,"end":30835300,"strand":1,"description":"TAB3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20176]"}, {"versioned_ensembl_gene_id":"ENSG00000062716.12","gene_symbol":"VMP1","gene_name":"vacuole membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29559]","synonyms":"TMEM49,TANGO5,EPG3","biotype":"protein_coding","ncbi_id":"81671","summary":"This gene encodes a transmembrane protein that plays a key regulatory role in the process of autophagy. The ectopic overexpression of the encoded protein in cultured cells triggers autophagy even under nutrient-rich conditions. This gene is overexpressed in pancreatitis affected acinar cells where the encoded protein mediates sequestration and degradation of potentially deleterious activated zymogen granules in a process termed, zymophagy. [provided by RefSeq, Jul 2016]","start":59707192,"end":59842255,"strand":1,"description":"vacuole membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29559]"}, {"versioned_ensembl_gene_id":"ENSG00000237906.1","gene_symbol":"MUPP","gene_name":"major urinary protein, pseudogene [Source:HGNC Symbol;Acc:HGNC:49202]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"100129193","summary":null,"start":112959134,"end":112962261,"strand":-1,"description":"major urinary protein, pseudogene [Source:HGNC Symbol;Acc:HGNC:49202]"}, {"versioned_ensembl_gene_id":"ENSG00000134717.17","gene_symbol":"BTF3L4","gene_name":"basic transcription factor 3 like 4 [Source:HGNC Symbol;Acc:HGNC:30547]","synonyms":"MGC23908","biotype":"protein_coding","ncbi_id":"91408","summary":null,"start":52056125,"end":52090716,"strand":1,"description":"basic transcription factor 3 like 4 [Source:HGNC Symbol;Acc:HGNC:30547]"}, {"versioned_ensembl_gene_id":"ENSG00000248925.1","gene_symbol":"AC021087.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":269858,"end":271516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141378.14","gene_symbol":"PTRH2","gene_name":"peptidyl-tRNA hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:24265]","synonyms":"PTH2,CGI-147,CFAP37,BIT1","biotype":"protein_coding","ncbi_id":"51651","summary":"The protein encoded by this gene is a mitochondrial protein with two putative domains, an N-terminal mitochondrial localization sequence, and a UPF0099 domain. In vitro assays suggest that this protein possesses peptidyl-tRNA hydrolase activity, to release the peptidyl moiety from tRNA, thereby preventing the accumulation of dissociated peptidyl-tRNA that could reduce the efficiency of translation. This protein also plays a role regulating cell survival and death. It promotes survival as part of an integrin-signaling pathway for cells attached to the extracellular matrix (ECM), but also promotes apoptosis in cells that have lost their attachment to the ECM, a process called anoikos. After loss of cell attachment to the ECM, this protein is phosphorylated, is released from the mitochondria into the cytosol, and promotes caspase-independent apoptosis through interactions with transcriptional regulators. This gene has been implicated in the development and progression of tumors, and mutations in this gene have been associated with an infantile multisystem neurologic, endocrine, and pancreatic disease (INMEPD) characterized by intellectual disability, postnatal microcephaly, progressive cerebellar atrophy, hearing impairment, polyneuropathy, failure to thrive, and organ fibrosis with exocrine pancreas insufficiency (PMID: 25574476). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]","start":59674636,"end":59707626,"strand":-1,"description":"peptidyl-tRNA hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:24265]"}, {"versioned_ensembl_gene_id":"ENSG00000258471.1","gene_symbol":"AL355922.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20995837,"end":20999163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257456.1","gene_symbol":"AC009320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29519731,"end":29529974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164106.7","gene_symbol":"SCRG1","gene_name":"stimulator of chondrogenesis 1 [Source:HGNC Symbol;Acc:HGNC:17036]","synonyms":"SCRG-1","biotype":"protein_coding","ncbi_id":"11341","summary":"Scrapie-responsive gene 1 is associated with neurodegenerative changes observed in transmissible spongiform encephalopathies. It may play a role in host response to prion-associated infections. The scrapie responsive protein 1 may be partly included in the membrane or secreted by the cells due to its hydrophobic N-terminus. In addition, the encoded protein can interact with bone marrow stromal cell antigen 1 (BST1) to enhance the differentiation potentials of human mesenchymal stem cells during tissue and bone regeneration. [provided by RefSeq, Jul 2016]","start":173384701,"end":173406380,"strand":-1,"description":"stimulator of chondrogenesis 1 [Source:HGNC Symbol;Acc:HGNC:17036]"}, {"versioned_ensembl_gene_id":"ENSG00000265415.1","gene_symbol":"AC099850.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59202677,"end":59203829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113719.15","gene_symbol":"ERGIC1","gene_name":"endoplasmic reticulum-golgi intermediate compartment 1 [Source:HGNC Symbol;Acc:HGNC:29205]","synonyms":"ERGIC-32,NET24,KIAA1181,ERGIC32","biotype":"protein_coding","ncbi_id":"57222","summary":"This gene encodes a cycling membrane protein which is an endoplasmic reticulum-golgi intermediate compartment (ERGIC) protein which interacts with other members of this protein family to increase their turnover. [provided by RefSeq, Jul 2008]","start":172834275,"end":172952685,"strand":1,"description":"endoplasmic reticulum-golgi intermediate compartment 1 [Source:HGNC Symbol;Acc:HGNC:29205]"}, {"versioned_ensembl_gene_id":"ENSG00000256843.1","gene_symbol":"AC023157.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31748100,"end":31748240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068489.12","gene_symbol":"PRR11","gene_name":"proline rich 11 [Source:HGNC Symbol;Acc:HGNC:25619]","synonyms":"FLJ11029","biotype":"protein_coding","ncbi_id":"55771","summary":null,"start":59155499,"end":59204705,"strand":1,"description":"proline rich 11 [Source:HGNC Symbol;Acc:HGNC:25619]"}, {"versioned_ensembl_gene_id":"ENSG00000258694.1","gene_symbol":"LINC02319","gene_name":"long intergenic non-protein coding RNA 2319 [Source:HGNC Symbol;Acc:HGNC:53238]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370498","summary":null,"start":52111122,"end":52129625,"strand":-1,"description":"long intergenic non-protein coding RNA 2319 [Source:HGNC Symbol;Acc:HGNC:53238]"}, {"versioned_ensembl_gene_id":"ENSG00000260937.5","gene_symbol":"AC025272.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55056747,"end":55092173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261872.1","gene_symbol":"AC002558.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47169826,"end":47171049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239291.1","gene_symbol":"AC002558.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47159191,"end":47159993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197019.4","gene_symbol":"SERTAD1","gene_name":"SERTA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17932]","synonyms":"TRIP-Br1,SEI1","biotype":"protein_coding","ncbi_id":"29950","summary":null,"start":40421592,"end":40426025,"strand":-1,"description":"SERTA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17932]"}, {"versioned_ensembl_gene_id":"ENSG00000249562.1","gene_symbol":"AC091885.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24578294,"end":24578561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119457.7","gene_symbol":"SLC46A2","gene_name":"solute carrier family 46 member 2 [Source:HGNC Symbol;Acc:HGNC:16055]","synonyms":"TSCOT,Ly110","biotype":"protein_coding","ncbi_id":"57864","summary":null,"start":112878920,"end":112890913,"strand":-1,"description":"solute carrier family 46 member 2 [Source:HGNC Symbol;Acc:HGNC:16055]"}, {"versioned_ensembl_gene_id":"ENSG00000271631.1","gene_symbol":"AL139041.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112885158,"end":112885767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228354.1","gene_symbol":"AL450023.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52655207,"end":52657254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255986.6","gene_symbol":"MT1JP","gene_name":"metallothionein 1J, pseudogene [Source:HGNC Symbol;Acc:HGNC:7402]","synonyms":"MTB,MT1NP,MT1J,MT1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4498","summary":null,"start":56635739,"end":56637086,"strand":1,"description":"metallothionein 1J, pseudogene [Source:HGNC Symbol;Acc:HGNC:7402]"}, {"versioned_ensembl_gene_id":"ENSG00000278699.4","gene_symbol":"POTEB3","gene_name":"POTE ankyrin domain family member B3 [Source:HGNC Symbol;Acc:HGNC:51240]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724631","summary":null,"start":21408280,"end":21440481,"strand":-1,"description":"POTE ankyrin domain family member B3 [Source:HGNC Symbol;Acc:HGNC:51240]"}, {"versioned_ensembl_gene_id":"ENSG00000227445.1","gene_symbol":"OR10R1P","gene_name":"olfactory receptor family 10 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14813]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79513","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158514785,"end":158515925,"strand":1,"description":"olfactory receptor family 10 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14813]"}, {"versioned_ensembl_gene_id":"ENSG00000236825.2","gene_symbol":"RAB28P2","gene_name":"RAB28, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50381]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129331","summary":null,"start":62606797,"end":62607748,"strand":-1,"description":"RAB28, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50381]"}, {"versioned_ensembl_gene_id":"ENSG00000242387.1","gene_symbol":"HIST1H2APS2","gene_name":"histone cluster 1 H2A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18804]","synonyms":"H2AFTP,H2A/T,dJ139G21.2","biotype":"transcribed_processed_pseudogene","ncbi_id":"85303","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 6. [provided by RefSeq, Oct 2015]","start":25882026,"end":25882395,"strand":-1,"description":"histone cluster 1 H2A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18804]"}, {"versioned_ensembl_gene_id":"ENSG00000235297.3","gene_symbol":"AC008021.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74389884,"end":74390297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117143.13","gene_symbol":"UAP1","gene_name":"UDP-N-acetylglucosamine pyrophosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:12457]","synonyms":"SPAG2,AGX1,AgX","biotype":"protein_coding","ncbi_id":"6675","summary":null,"start":162561506,"end":162599842,"strand":1,"description":"UDP-N-acetylglucosamine pyrophosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:12457]"}, {"versioned_ensembl_gene_id":"ENSG00000278528.1","gene_symbol":"AC145285.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28773824,"end":28777534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250473.1","gene_symbol":"DUTP7","gene_name":"deoxyuridine triphosphatase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39520]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873913","summary":null,"start":51865050,"end":51865535,"strand":-1,"description":"deoxyuridine triphosphatase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39520]"}, {"versioned_ensembl_gene_id":"ENSG00000198965.4","gene_symbol":"OR10R2","gene_name":"olfactory receptor family 10 subfamily R member 2 [Source:HGNC Symbol;Acc:HGNC:14820]","synonyms":"OR10R2Q","biotype":"protein_coding","ncbi_id":"343406","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158472220,"end":158480936,"strand":1,"description":"olfactory receptor family 10 subfamily R member 2 [Source:HGNC Symbol;Acc:HGNC:14820]"}, {"versioned_ensembl_gene_id":"ENSG00000250486.3","gene_symbol":"FAM218A","gene_name":"family with sequence similarity 218 member A [Source:HGNC Symbol;Acc:HGNC:26466]","synonyms":"C4orf39,FLJ31659","biotype":"protein_coding","ncbi_id":"152756","summary":null,"start":164956948,"end":164959122,"strand":1,"description":"family with sequence similarity 218 member A [Source:HGNC Symbol;Acc:HGNC:26466]"}, {"versioned_ensembl_gene_id":"ENSG00000254728.1","gene_symbol":"AC027369.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48881723,"end":48902181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227879.2","gene_symbol":"PSPC1P1","gene_name":"paraspeckle component 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42033]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642395","summary":null,"start":19201637,"end":19227432,"strand":-1,"description":"paraspeckle component 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42033]"}, {"versioned_ensembl_gene_id":"ENSG00000258967.1","gene_symbol":"AL117694.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68887785,"end":68888084,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242289.1","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"processed_transcript","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29422681,"end":29432038,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000136643.11","gene_symbol":"RPS6KC1","gene_name":"ribosomal protein S6 kinase C1 [Source:HGNC Symbol;Acc:HGNC:10439]","synonyms":"humS6PKh1","biotype":"protein_coding","ncbi_id":"26750","summary":"Sphingosine kinase catalyzes the formation of sphingosine 1 phosphate, a lipid cellular messenger. The protein encoded by this gene can bind to sphingosine kinase and to phosphatidylinositol 3-phosphate, suggesting a role in sphingosine 1 phophate signaling. The encoded protein can also bind to peroxiredoxin-3 and may help transport it to mitochondria. [provided by RefSeq, Mar 2017]","start":213051233,"end":213274773,"strand":1,"description":"ribosomal protein S6 kinase C1 [Source:HGNC Symbol;Acc:HGNC:10439]"}, {"versioned_ensembl_gene_id":"ENSG00000164256.10","gene_symbol":"PRDM9","gene_name":"PR/SET domain 9 [Source:HGNC Symbol;Acc:HGNC:13994]","synonyms":"ZNF899,PFM6,MSBP3,KMT8B","biotype":"protein_coding","ncbi_id":"56979","summary":"The protein encoded by this gene is a zinc finger protein with histone methyltransferase activity that catalyzes histone H3 lysine 4 trimethylation (H3K4me3) during meiotic prophase. This protein contains multiple domains, including a Kruppel-associated box (KRAB) domain, an SSX repression domain (SSXRD), a PRD1-BF1 and RIZ homologous region, a subclass of SET (PR/SET) domain, and a tandem array of C2H2 zinc fingers. The zinc finger array recognizes a short sequence motif, leading to local H3K4me3, and meiotic recombination hotspot activity. The observed allelic variation alters the DNA-binding sequence specificity of the protein, resulting in distinct meiotic recombination hotspots amongst individuals and populations. Multiple alternate alleles of this gene have been described. [provided by RefSeq, Jul 2015]","start":23443586,"end":23528597,"strand":1,"description":"PR/SET domain 9 [Source:HGNC Symbol;Acc:HGNC:13994]"}, {"versioned_ensembl_gene_id":"ENSG00000224229.1","gene_symbol":"CR942175.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29124236,"end":29128934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260123.1","gene_symbol":"AC013565.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89041223,"end":89082819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280631.1","gene_symbol":"AC233280.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260275.1","gene_symbol":"AC013565.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89037977,"end":89038286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204382.11","gene_symbol":"XAGE1B","gene_name":"X antigen family member 1B [Source:HGNC Symbol;Acc:HGNC:25400]","synonyms":"CT12.1b","biotype":"protein_coding","ncbi_id":"653220","summary":"This gene is a member of the XAGE subfamily, which belongs to the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. This gene is strongly expressed in Ewing's sarcoma, alveolar rhabdomyosarcoma and normal testis. The protein encoded by this gene contains a nuclear localization signal and shares a sequence similarity with other GAGE/PAGE proteins. Because of the expression pattern and the sequence similarity, this protein also belongs to a family of CT (cancer-testis) antigens. Alternative splicing of this gene, in addition to alternative transcription start sites, results in multiple transcript variants. [provided by RefSeq, Jan 2010]","start":52512077,"end":52520803,"strand":-1,"description":"X antigen family member 1B [Source:HGNC Symbol;Acc:HGNC:25400]"}, {"versioned_ensembl_gene_id":"ENSG00000272679.1","gene_symbol":"AL355987.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":136800366,"end":136829466,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140400.16","gene_symbol":"MAN2C1","gene_name":"mannosidase alpha class 2C member 1 [Source:HGNC Symbol;Acc:HGNC:6827]","synonyms":"MANA1,MANA","biotype":"protein_coding","ncbi_id":"4123","summary":null,"start":75355207,"end":75368630,"strand":-1,"description":"mannosidase alpha class 2C member 1 [Source:HGNC Symbol;Acc:HGNC:6827]"}, {"versioned_ensembl_gene_id":"ENSG00000197530.12","gene_symbol":"MIB2","gene_name":"mindbomb E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:30577]","synonyms":"ZZZ5,ZZANK1,FLJ39787,skeletrophin","biotype":"protein_coding","ncbi_id":"142678","summary":"The protein encoded by this gene is an E3 ubiquitin protein ligase that mediates ubiquitination of proteins in the Notch signaling pathway. The encoded protein may be a suppressor of melanoma invasion. [provided by RefSeq, Mar 2017]","start":1615415,"end":1630610,"strand":1,"description":"mindbomb E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:30577]"}, {"versioned_ensembl_gene_id":"ENSG00000278213.1","gene_symbol":"CNTNAP3P5","gene_name":"contactin associated protein-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49588]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420786","summary":null,"start":62559839,"end":62569907,"strand":1,"description":"contactin associated protein-like 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49588]"}, {"versioned_ensembl_gene_id":"ENSG00000243810.1","gene_symbol":"AL121721.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20258407,"end":20267809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241408.1","gene_symbol":"CR759957.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28986792,"end":28988567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276058.1","gene_symbol":"STMN1P1","gene_name":"stathmin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506685","summary":null,"start":31715342,"end":31715781,"strand":-1,"description":"stathmin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44062]"}, {"versioned_ensembl_gene_id":"ENSG00000281208.1","gene_symbol":"AC136352.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21344605,"end":21345142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232664.2","gene_symbol":"LARP1BP3","gene_name":"La ribonucleoprotein domain family member 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44085]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644403","summary":null,"start":134204353,"end":134205916,"strand":1,"description":"La ribonucleoprotein domain family member 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44085]"}, {"versioned_ensembl_gene_id":"ENSG00000187116.13","gene_symbol":"LILRA5","gene_name":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]","synonyms":"CD85,LILRB7,ILT11,CD85f,LIR9","biotype":"protein_coding","ncbi_id":"353514","summary":"The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":54307070,"end":54313139,"strand":-1,"description":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]"}, {"versioned_ensembl_gene_id":"ENSG00000267153.1","gene_symbol":"CTBP2P3","gene_name":"C-terminal binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45195]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"220147","summary":null,"start":60663115,"end":60664369,"strand":1,"description":"C-terminal binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45195]"}, {"versioned_ensembl_gene_id":"ENSG00000266783.1","gene_symbol":"AP005136.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2561172,"end":2562220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224603.1","gene_symbol":"BX664725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62444256,"end":62444634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235817.2","gene_symbol":"AL158214.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":230612009,"end":230612412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223531.9","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30181379,"end":30191586,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000233381.3","gene_symbol":"AK4P3","gene_name":"adenylate kinase 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21596]","synonyms":"AK3L2P,AK3L2","biotype":"processed_pseudogene","ncbi_id":"645619","summary":null,"start":31615771,"end":31616439,"strand":-1,"description":"adenylate kinase 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21596]"}, {"versioned_ensembl_gene_id":"ENSG00000234894.1","gene_symbol":"AL139327.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19151554,"end":19152307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237738.1","gene_symbol":"RNF216-IT1","gene_name":"RNF216 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41463]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874342","summary":null,"start":5662432,"end":5680461,"strand":-1,"description":"RNF216 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41463]"}, {"versioned_ensembl_gene_id":"ENSG00000138035.14","gene_symbol":"PNPT1","gene_name":"polyribonucleotide nucleotidyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23166]","synonyms":"PNPase,OLD35,old-35,DFNB70","biotype":"protein_coding","ncbi_id":"87178","summary":"The protein encoded by this gene belongs to the evolutionary conserved polynucleotide phosphorylase family comprised of phosphate dependent 3'-to-5' exoribonucleases implicated in RNA processing and degradation. This enzyme is predominantly localized in the mitochondrial intermembrane space and is involved in import of RNA to mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70. Related pseudogenes are found on chromosomes 3 and 7. [provided by RefSeq, Dec 2012]","start":55634265,"end":55693910,"strand":-1,"description":"polyribonucleotide nucleotidyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23166]"}, {"versioned_ensembl_gene_id":"ENSG00000091137.11","gene_symbol":"SLC26A4","gene_name":"solute carrier family 26 member 4 [Source:HGNC Symbol;Acc:HGNC:8818]","synonyms":"PDS,DFNB4","biotype":"protein_coding","ncbi_id":"5172","summary":"Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008]","start":107660635,"end":107717809,"strand":1,"description":"solute carrier family 26 member 4 [Source:HGNC Symbol;Acc:HGNC:8818]"}, {"versioned_ensembl_gene_id":"ENSG00000112996.10","gene_symbol":"MRPS30","gene_name":"mitochondrial ribosomal protein S30 [Source:HGNC Symbol;Acc:HGNC:8769]","synonyms":"PDCD9,PAP","biotype":"protein_coding","ncbi_id":"10884","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that is similar to the chicken pro-apoptotic protein p52. Transcript variants using alternative promoters or polyA sites have been mentioned in the literature but the complete description of these sequences is not available. [provided by RefSeq, Jul 2008]","start":44808925,"end":44820428,"strand":1,"description":"mitochondrial ribosomal protein S30 [Source:HGNC Symbol;Acc:HGNC:8769]"}, {"versioned_ensembl_gene_id":"ENSG00000254332.1","gene_symbol":"AF201337.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69129598,"end":69130345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261670.1","gene_symbol":"AC012213.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103464389,"end":103468985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235737.1","gene_symbol":"TRIM60P19","gene_name":"tripartite motif containing 60 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42010]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533672","summary":null,"start":66268997,"end":66270458,"strand":1,"description":"tripartite motif containing 60 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42010]"}, {"versioned_ensembl_gene_id":"ENSG00000254399.2","gene_symbol":"GLYATL1P4","gene_name":"glycine-N-acyltransferase like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37864]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643637","summary":null,"start":59042737,"end":59050971,"strand":1,"description":"glycine-N-acyltransferase like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37864]"}, {"versioned_ensembl_gene_id":"ENSG00000260231.1","gene_symbol":"JHDM1D-AS1","gene_name":"JHDM1D antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48959]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100134229","summary":null,"start":140177261,"end":140179640,"strand":1,"description":"JHDM1D antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48959]"}, {"versioned_ensembl_gene_id":"ENSG00000227006.1","gene_symbol":"AL136988.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230258694,"end":230268483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224407.1","gene_symbol":"AL136988.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230280312,"end":230281893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250954.5","gene_symbol":"AC016687.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33776347,"end":34039893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273274.1","gene_symbol":"ZBTB8B","gene_name":"zinc finger and BTB domain containing 8B [Source:HGNC Symbol;Acc:HGNC:37057]","synonyms":"ZNF916B,RP1-27O5.1,DKFZp547H154","biotype":"protein_coding","ncbi_id":"728116","summary":null,"start":32465069,"end":32496686,"strand":1,"description":"zinc finger and BTB domain containing 8B [Source:HGNC Symbol;Acc:HGNC:37057]"}, {"versioned_ensembl_gene_id":"ENSG00000279804.2","gene_symbol":"PRAMEF18","gene_name":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391003","summary":null,"start":13222705,"end":13226106,"strand":-1,"description":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]"}, {"versioned_ensembl_gene_id":"ENSG00000175334.7","gene_symbol":"BANF1","gene_name":"barrier to autointegration factor 1 [Source:HGNC Symbol;Acc:HGNC:17397]","synonyms":"BAF","biotype":"protein_coding","ncbi_id":"8815","summary":"The protein encoded by this gene was first identified by its ability to protect retroviruses from intramolecular integration and therefore promote intermolecular integration into the host cell genome. The protein forms a homodimer which localizes to both the nucleus and cytoplasm and is specifically associated with chromosomes during mitosis. This protein binds to double stranded DNA in a non-specific manner and also binds to LEM-domain containing proteins of the nuclear envelope. This protein is thought to facilitate nuclear reassembly by binding with both DNA and inner nuclear membrane proteins and thereby recruit chromatin to the nuclear periphery. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Jan 2009]","start":66002079,"end":66004149,"strand":1,"description":"barrier to autointegration factor 1 [Source:HGNC Symbol;Acc:HGNC:17397]"}, {"versioned_ensembl_gene_id":"ENSG00000234622.6","gene_symbol":"AL683807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1767347,"end":1768776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224855.5","gene_symbol":"OPA1-AS1","gene_name":"OPA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40421]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873941","summary":null,"start":193618609,"end":193627337,"strand":-1,"description":"OPA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40421]"}, {"versioned_ensembl_gene_id":"ENSG00000170075.8","gene_symbol":"GPR37L1","gene_name":"G protein-coupled receptor 37 like 1 [Source:HGNC Symbol;Acc:HGNC:14923]","synonyms":"ETBR-LP-2","biotype":"protein_coding","ncbi_id":"9283","summary":null,"start":202122858,"end":202133592,"strand":1,"description":"G protein-coupled receptor 37 like 1 [Source:HGNC Symbol;Acc:HGNC:14923]"}, {"versioned_ensembl_gene_id":"ENSG00000042813.7","gene_symbol":"ZPBP","gene_name":"zona pellucida binding protein [Source:HGNC Symbol;Acc:HGNC:15662]","synonyms":"ZPBP1,SP38","biotype":"protein_coding","ncbi_id":"11055","summary":"ZPBP is one of several proteins that are thought to participate in secondary binding between acrosome-reacted sperm and the egg-specific extracellular matrix, the zona pellucida (McLeskey et al., 1998 [PubMed 9378618]).[supplied by OMIM, Aug 2008]","start":49850421,"end":50121329,"strand":-1,"description":"zona pellucida binding protein [Source:HGNC Symbol;Acc:HGNC:15662]"}, {"versioned_ensembl_gene_id":"ENSG00000226042.1","gene_symbol":"CDY10P","gene_name":"chromodomain Y-linked 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:23848]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"140043","summary":null,"start":21637475,"end":21639041,"strand":-1,"description":"chromodomain Y-linked 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:23848]"}, {"versioned_ensembl_gene_id":"ENSG00000196262.13","gene_symbol":"PPIA","gene_name":"peptidylprolyl isomerase A [Source:HGNC Symbol;Acc:HGNC:9253]","synonyms":"CYPA","biotype":"protein_coding","ncbi_id":"5478","summary":"This gene encodes a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. The encoded protein is a cyclosporin binding-protein and may play a role in cyclosporin A-mediated immunosuppression. The protein can also interact with several HIV proteins, including p55 gag, Vpr, and capsid protein, and has been shown to be necessary for the formation of infectious HIV virions. Multiple pseudogenes that map to different chromosomes have been reported. [provided by RefSeq, Jul 2008]","start":44796680,"end":44824564,"strand":1,"description":"peptidylprolyl isomerase A [Source:HGNC Symbol;Acc:HGNC:9253]"}, {"versioned_ensembl_gene_id":"ENSG00000124198.8","gene_symbol":"ARFGEF2","gene_name":"ADP ribosylation factor guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:15853]","synonyms":"BIG2","biotype":"protein_coding","ncbi_id":"10564","summary":"ADP-ribosylation factors (ARFs) play an important role in intracellular vesicular trafficking. The protein encoded by this gene is involved in the activation of ARFs by accelerating replacement of bound GDP with GTP and is involved in Golgi transport. It contains a Sec7 domain, which may be responsible for its guanine-nucleotide exchange activity and also brefeldin A inhibition. [provided by RefSeq, Jul 2008]","start":48921890,"end":49036693,"strand":1,"description":"ADP ribosylation factor guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:15853]"}, {"versioned_ensembl_gene_id":"ENSG00000249488.1","gene_symbol":"NACAP5","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49492]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645108","summary":null,"start":17552117,"end":17552752,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49492]"}, {"versioned_ensembl_gene_id":"ENSG00000143337.18","gene_symbol":"TOR1AIP1","gene_name":"torsin 1A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29456]","synonyms":"LAP1B,FLJ13142","biotype":"protein_coding","ncbi_id":"26092","summary":"This gene encodes a type 2 integral membrane protein that binds A- and B-type lamins. The encoded protein localizes to the inner nuclear membrane and may be involved in maintaining the attachment of the nuclear membrane to the nuclear lamina during cell division. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":179882042,"end":179925000,"strand":1,"description":"torsin 1A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29456]"}, {"versioned_ensembl_gene_id":"ENSG00000146278.10","gene_symbol":"PNRC1","gene_name":"proline rich nuclear receptor coactivator 1 [Source:HGNC Symbol;Acc:HGNC:17278]","synonyms":"PRR2,PROL2,B4-2","biotype":"protein_coding","ncbi_id":"10957","summary":null,"start":89080751,"end":89085160,"strand":1,"description":"proline rich nuclear receptor coactivator 1 [Source:HGNC Symbol;Acc:HGNC:17278]"}, {"versioned_ensembl_gene_id":"ENSG00000235888.1","gene_symbol":"AF064858.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38988707,"end":39006153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228685.1","gene_symbol":"AL365356.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5624931,"end":5625126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227109.1","gene_symbol":"CRIP1P3","gene_name":"cysteine rich protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479040","summary":null,"start":202096759,"end":202096978,"strand":1,"description":"cysteine rich protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44518]"}, {"versioned_ensembl_gene_id":"ENSG00000232774.7","gene_symbol":"FLJ22447","gene_name":"uncharacterized LOC400221 [Source:NCBI gene;Acc:400221]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400221","summary":null,"start":61570540,"end":61658696,"strand":1,"description":"uncharacterized LOC400221 [Source:NCBI gene;Acc:400221]"}, {"versioned_ensembl_gene_id":"ENSG00000234411.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28896521,"end":28897313,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000220131.1","gene_symbol":"AL121835.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88265158,"end":88265511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152558.14","gene_symbol":"TMEM123","gene_name":"transmembrane protein 123 [Source:HGNC Symbol;Acc:HGNC:30138]","synonyms":"PORIMIN,KCT3","biotype":"protein_coding","ncbi_id":"114908","summary":"This gene encodes a highly glycosylated transmembrane protein with a high content of threonine and serine residues in its extracellular domain, similar to a broadly defined category of proteins termed mucins. Exposure of some cell types to anti-PORIMIN (pro-oncosis receptor inducing membrane injury) antibody, crosslinks this protein on the cell surface and induces a type of cell death termed oncosis. Oncosis is distinct from apoptosis and is characterized by a loss of cell membrane integrity without DNA fragmentation. This gene product is proposed to function as a cell surface receptor that mediates cell death. [provided by RefSeq, Jul 2008]","start":102396332,"end":102470384,"strand":-1,"description":"transmembrane protein 123 [Source:HGNC Symbol;Acc:HGNC:30138]"}, {"versioned_ensembl_gene_id":"ENSG00000232642.1","gene_symbol":"AC008073.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24165884,"end":24175005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237559.1","gene_symbol":"HLA-S","gene_name":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]","synonyms":"HLA-17","biotype":"unprocessed_pseudogene","ncbi_id":"267015","summary":null,"start":31372160,"end":31372374,"strand":-1,"description":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]"}, {"versioned_ensembl_gene_id":"ENSG00000260986.1","gene_symbol":"AC126335.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21127698,"end":21130095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279595.1","gene_symbol":"AC126335.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21148334,"end":21152970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232276.1","gene_symbol":"AL845443.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31367516,"end":31368113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254442.1","gene_symbol":"AP000859.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134316782,"end":134317088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273980.1","gene_symbol":"AL592071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133257144,"end":133257551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236992.2","gene_symbol":"RPL12P12","gene_name":"ribosomal protein L12 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:15951]","synonyms":"RPL12L3,dJ999L4.1","biotype":"processed_pseudogene","ncbi_id":"85824","summary":null,"start":19823443,"end":19823943,"strand":-1,"description":"ribosomal protein L12 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:15951]"}, {"versioned_ensembl_gene_id":"ENSG00000171320.14","gene_symbol":"ESCO2","gene_name":"establishment of sister chromatid cohesion N-acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:27230]","synonyms":"RBS,EFO2","biotype":"protein_coding","ncbi_id":"157570","summary":"This gene encodes a protein that may have acetyltransferase activity and may be required for the establishment of sister chromatid cohesion during the S phase of mitosis. Mutations in this gene have been associated with Roberts syndrome. [provided by RefSeq, Jul 2008]","start":27771949,"end":27812640,"strand":1,"description":"establishment of sister chromatid cohesion N-acetyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:27230]"}, {"versioned_ensembl_gene_id":"ENSG00000234674.6","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31153422,"end":31159096,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000260976.1","gene_symbol":"LINC01633","gene_name":"long intergenic non-protein coding RNA 1633 [Source:HGNC Symbol;Acc:HGNC:52420]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929069","summary":null,"start":185001527,"end":185008683,"strand":1,"description":"long intergenic non-protein coding RNA 1633 [Source:HGNC Symbol;Acc:HGNC:52420]"}, {"versioned_ensembl_gene_id":"ENSG00000260899.1","gene_symbol":"AC106886.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30740667,"end":30751381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261840.2","gene_symbol":"AC093249.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30697707,"end":30699058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228365.1","gene_symbol":"AL133351.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2916894,"end":2917733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163817.15","gene_symbol":"SLC6A20","gene_name":"solute carrier family 6 member 20 [Source:HGNC Symbol;Acc:HGNC:30927]","synonyms":"Xtrp3,XT3","biotype":"protein_coding","ncbi_id":"54716","summary":"Transport of small hydrophilic substances across cell membranes is mediated by substrate-specific transporter proteins which have been classified into several families of related genes. The protein encoded by this gene belongs to the sodium:neurotransmitter symporter (SNF) family and functions as a proline transporter expressed in kidney and small intestine. Mutations in this gene are associated with Hyperglycinuria and Iminoglycinuria. [provided by RefSeq, Jul 2020]","start":45755450,"end":45796535,"strand":-1,"description":"solute carrier family 6 member 20 [Source:HGNC Symbol;Acc:HGNC:30927]"}, {"versioned_ensembl_gene_id":"ENSG00000116761.11","gene_symbol":"CTH","gene_name":"cystathionine gamma-lyase [Source:HGNC Symbol;Acc:HGNC:2501]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1491","summary":"This gene encodes a cytoplasmic enzyme in the trans-sulfuration pathway that converts cystathione derived from methionine into cysteine. Glutathione synthesis in the liver is dependent upon the availability of cysteine. Mutations in this gene cause cystathioninuria. Alternative splicing of this gene results in three transcript variants encoding different isoforms. [provided by RefSeq, Jun 2010]","start":70411218,"end":70439851,"strand":1,"description":"cystathionine gamma-lyase [Source:HGNC Symbol;Acc:HGNC:2501]"}, {"versioned_ensembl_gene_id":"ENSG00000235554.1","gene_symbol":"AC005822.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16616848,"end":16617881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102934.9","gene_symbol":"PLLP","gene_name":"plasmolipin [Source:HGNC Symbol;Acc:HGNC:18553]","synonyms":"TM4SF11,PMLP","biotype":"protein_coding","ncbi_id":"51090","summary":null,"start":57248547,"end":57284687,"strand":-1,"description":"plasmolipin [Source:HGNC Symbol;Acc:HGNC:18553]"}, {"versioned_ensembl_gene_id":"ENSG00000242457.1","gene_symbol":"RBBP4P2","gene_name":"RB binding protein 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420527","summary":null,"start":94075912,"end":94077175,"strand":-1,"description":"RB binding protein 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42369]"}, {"versioned_ensembl_gene_id":"ENSG00000250386.1","gene_symbol":"AC233724.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17625551,"end":17625959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137648.17","gene_symbol":"TMPRSS4","gene_name":"transmembrane protease, serine 4 [Source:HGNC Symbol;Acc:HGNC:11878]","synonyms":"TMPRSS3,MT-SP2","biotype":"protein_coding","ncbi_id":"56649","summary":"This gene encodes a member of the serine protease family. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified as a gene overexpressed in pancreatic carcinoma. The encoded protein is membrane bound with a N-terminal anchor sequence and a glycosylated extracellular region containing the serine protease domain. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":118077012,"end":118121890,"strand":1,"description":"transmembrane protease, serine 4 [Source:HGNC Symbol;Acc:HGNC:11878]"}, {"versioned_ensembl_gene_id":"ENSG00000227471.8","gene_symbol":"AKR1B15","gene_name":"aldo-keto reductase family 1 member B15 [Source:HGNC Symbol;Acc:HGNC:37281]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441282","summary":null,"start":134549136,"end":134579875,"strand":1,"description":"aldo-keto reductase family 1 member B15 [Source:HGNC Symbol;Acc:HGNC:37281]"}, {"versioned_ensembl_gene_id":"ENSG00000254000.1","gene_symbol":"AC090753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123924759,"end":123925933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203363.2","gene_symbol":"AC012454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85686053,"end":85687047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249647.2","gene_symbol":"C5orf66-AS2","gene_name":"C5orf66 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:27964]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340073","summary":null,"start":135236234,"end":135248179,"strand":-1,"description":"C5orf66 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:27964]"}, {"versioned_ensembl_gene_id":"ENSG00000284619.1","gene_symbol":"AC079776.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":129988158,"end":129990530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277619.1","gene_symbol":"AC008406.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135034521,"end":135035894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260109.1","gene_symbol":"AC135628.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67985059,"end":67986288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224067.2","gene_symbol":"AL354877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111802980,"end":111803435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235081.1","gene_symbol":"AC245052.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54229036,"end":54230213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271426.1","gene_symbol":"AL109983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13073667,"end":13074312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272789.1","gene_symbol":"AC010976.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127625997,"end":127626848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228492.2","gene_symbol":"RAB11FIP1P1","gene_name":"RAB11 family interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646080","summary":null,"start":74202834,"end":74204595,"strand":1,"description":"RAB11 family interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42366]"}, {"versioned_ensembl_gene_id":"ENSG00000224430.2","gene_symbol":"MKRN5P","gene_name":"makorin ring finger protein 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:7117]","synonyms":"ZNF127L2,ZNF-Xq,MKRNP1","biotype":"processed_pseudogene","ncbi_id":"7683","summary":null,"start":74161062,"end":74162528,"strand":-1,"description":"makorin ring finger protein 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:7117]"}, {"versioned_ensembl_gene_id":"ENSG00000154945.6","gene_symbol":"ANKRD40","gene_name":"ankyrin repeat domain 40 [Source:HGNC Symbol;Acc:HGNC:28233]","synonyms":"MGC15396","biotype":"protein_coding","ncbi_id":"91369","summary":null,"start":50693190,"end":50707924,"strand":-1,"description":"ankyrin repeat domain 40 [Source:HGNC Symbol;Acc:HGNC:28233]"}, {"versioned_ensembl_gene_id":"ENSG00000007952.17","gene_symbol":"NOX1","gene_name":"NADPH oxidase 1 [Source:HGNC Symbol;Acc:HGNC:7889]","synonyms":"NOH1,NOH-1,MOX1,GP91-2","biotype":"protein_coding","ncbi_id":"27035","summary":"This gene encodes a member of the NADPH oxidase family of enzymes responsible for the catalytic one-electron transfer of oxygen to generate superoxide or hydrogen peroxide. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]","start":100843324,"end":100874345,"strand":-1,"description":"NADPH oxidase 1 [Source:HGNC Symbol;Acc:HGNC:7889]"}, {"versioned_ensembl_gene_id":"ENSG00000272483.1","gene_symbol":"AC022001.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11611602,"end":11612197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259612.1","gene_symbol":"EEF1A1P22","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37895]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645693","summary":null,"start":52937139,"end":52938518,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37895]"}, {"versioned_ensembl_gene_id":"ENSG00000278687.1","gene_symbol":"AC024255.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28978584,"end":28978685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245479.2","gene_symbol":"LINC01585","gene_name":"long intergenic non-protein coding RNA 1585 [Source:HGNC Symbol;Acc:HGNC:51432]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"101929765","summary":null,"start":90660234,"end":90664967,"strand":1,"description":"long intergenic non-protein coding RNA 1585 [Source:HGNC Symbol;Acc:HGNC:51432]"}, {"versioned_ensembl_gene_id":"ENSG00000279897.1","gene_symbol":"BIRC6-AS2","gene_name":"BIRC6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:50490]","synonyms":"megamind","biotype":"antisense_RNA","ncbi_id":"103752586","summary":null,"start":32557520,"end":32574818,"strand":-1,"description":"BIRC6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:50490]"}, {"versioned_ensembl_gene_id":"ENSG00000160062.14","gene_symbol":"ZBTB8A","gene_name":"zinc finger and BTB domain containing 8A [Source:HGNC Symbol;Acc:HGNC:24172]","synonyms":"ZBTB8,FLJ90065,BOZF1,ZNF916A","biotype":"protein_coding","ncbi_id":"653121","summary":null,"start":32539427,"end":32605939,"strand":1,"description":"zinc finger and BTB domain containing 8A [Source:HGNC Symbol;Acc:HGNC:24172]"}, {"versioned_ensembl_gene_id":"ENSG00000229607.1","gene_symbol":"AL137027.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30810378,"end":30815553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224197.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32659420,"end":32660356,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000272914.1","gene_symbol":"AL359532.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30831828,"end":30833387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248842.1","gene_symbol":"AC011396.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146400981,"end":146407359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110330.8","gene_symbol":"BIRC2","gene_name":"baculoviral IAP repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:590]","synonyms":"MIHB,hiap-2,cIAP1,c-IAP1,API1,RNF48","biotype":"protein_coding","ncbi_id":"329","summary":"The protein encoded by this gene is a member of a family of proteins that inhibits apoptosis by binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2, probably by interfering with activation of ICE-like proteases. This encoded protein inhibits apoptosis induced by serum deprivation and menadione, a potent inducer of free radicals. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":102347211,"end":102378670,"strand":1,"description":"baculoviral IAP repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:590]"}, {"versioned_ensembl_gene_id":"ENSG00000165259.13","gene_symbol":"HDX","gene_name":"highly divergent homeobox [Source:HGNC Symbol;Acc:HGNC:26411]","synonyms":"FLJ30678,CXorf43","biotype":"protein_coding","ncbi_id":"139324","summary":null,"start":84317874,"end":84502479,"strand":-1,"description":"highly divergent homeobox [Source:HGNC Symbol;Acc:HGNC:26411]"}, {"versioned_ensembl_gene_id":"ENSG00000270824.1","gene_symbol":"IGHD5OR15-5B","gene_name":"immunoglobulin heavy diversity 5/OR15-5B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5513]","synonyms":"IGHD5OR155B,IGHD5/OR15-5B","biotype":"IG_D_gene","ncbi_id":"28326","summary":null,"start":21010494,"end":21010516,"strand":-1,"description":"immunoglobulin heavy diversity 5/OR15-5B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5513]"}, {"versioned_ensembl_gene_id":"ENSG00000271185.1","gene_symbol":"AC007029.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10940423,"end":10940735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116406.18","gene_symbol":"EDEM3","gene_name":"ER degradation enhancing alpha-mannosidase like protein 3 [Source:HGNC Symbol;Acc:HGNC:16787]","synonyms":"C1orf22","biotype":"protein_coding","ncbi_id":"80267","summary":"Quality control in the endoplasmic reticulum (ER) ensures that only properly folded proteins are retained in the cell through recognition and degradation of misfolded or unassembled proteins. EDEM3 belongs to a group of proteins that accelerate degradation of misfolded glycoproteins in the ER (Hirao et al., 2006 [PubMed 16431915]).[supplied by OMIM, Mar 2008]","start":184690231,"end":184754913,"strand":-1,"description":"ER degradation enhancing alpha-mannosidase like protein 3 [Source:HGNC Symbol;Acc:HGNC:16787]"}, {"versioned_ensembl_gene_id":"ENSG00000086967.9","gene_symbol":"MYBPC2","gene_name":"myosin binding protein C, fast type [Source:HGNC Symbol;Acc:HGNC:7550]","synonyms":"MYBPCF,MYBPC,MGC163408","biotype":"protein_coding","ncbi_id":"4606","summary":"This gene encodes a member of the myosin-binding protein C family. This family includes the fast-, slow- and cardiac-type isoforms, each of which is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The protein encoded by this locus is referred to as the fast-type isoform. Mutations in the related but distinct genes encoding the slow-type and cardiac-type isoforms have been associated with distal arthrogryposis, type 1 and hypertrophic cardiomyopathy, respectively. [provided by RefSeq, Jul 2012]","start":50432903,"end":50466321,"strand":1,"description":"myosin binding protein C, fast type [Source:HGNC Symbol;Acc:HGNC:7550]"}, {"versioned_ensembl_gene_id":"ENSG00000224194.1","gene_symbol":"AC008278.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15668684,"end":15680484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240486.2","gene_symbol":"RPL23AP54","gene_name":"ribosomal protein L23a pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36689]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271466","summary":null,"start":5476548,"end":5476966,"strand":1,"description":"ribosomal protein L23a pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:36689]"}, {"versioned_ensembl_gene_id":"ENSG00000283317.1","gene_symbol":"AL831711.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161433444,"end":161440996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277808.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156104,"end":54160226,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000279730.2","gene_symbol":"SETD8P1","gene_name":"SET domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30088]","synonyms":"SET07p","biotype":"processed_pseudogene","ncbi_id":"57108","summary":null,"start":18297554,"end":18298733,"strand":1,"description":"SET domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30088]"}, {"versioned_ensembl_gene_id":"ENSG00000224333.1","gene_symbol":"GAPDHP20","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343338","summary":null,"start":32402109,"end":32403115,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:37772]"}, {"versioned_ensembl_gene_id":"ENSG00000249697.1","gene_symbol":"AC034245.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56313905,"end":56321397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248781.1","gene_symbol":"PSMC1P4","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"345645","summary":null,"start":56275304,"end":56276630,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39779]"}, {"versioned_ensembl_gene_id":"ENSG00000284679.1","gene_symbol":"AL356585.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18248913,"end":18249035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278256.1","gene_symbol":"AC007718.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5363371,"end":5363650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261060.1","gene_symbol":"AL160286.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":179590372,"end":179591305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279302.3","gene_symbol":"AC013643.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":27701194,"end":27703789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205426.10","gene_symbol":"KRT81","gene_name":"keratin 81 [Source:HGNC Symbol;Acc:HGNC:6458]","synonyms":"KRTHB1,Hb-1","biotype":"protein_coding","ncbi_id":"3887","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB3 and KRTHB6, is found primarily in the hair cortex. Mutations in this gene and KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. [provided by RefSeq, Jul 2008]","start":52285913,"end":52291534,"strand":-1,"description":"keratin 81 [Source:HGNC Symbol;Acc:HGNC:6458]"}, {"versioned_ensembl_gene_id":"ENSG00000185379.20","gene_symbol":"RAD51D","gene_name":"RAD51 paralog D [Source:HGNC Symbol;Acc:HGNC:9823]","synonyms":"Trad,RAD51L3,R51H3,HsTRAD","biotype":"protein_coding","ncbi_id":"5892","summary":"The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51, which are known to be involved in the homologous recombination and repair of DNA. This protein forms a complex with several other members of the RAD51 family, including RAD51L1, RAD51L2, and XRCC2. The protein complex formed with this protein has been shown to catalyze homologous pairing between single- and double-stranded DNA, and is thought to play a role in the early stage of recombinational repair of DNA. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream ring finger and FYVE-like domain containing 1 (RFFL) gene. [provided by RefSeq, Jan 2011]","start":35092208,"end":35121522,"strand":-1,"description":"RAD51 paralog D [Source:HGNC Symbol;Acc:HGNC:9823]"}, {"versioned_ensembl_gene_id":"ENSG00000248008.2","gene_symbol":"NRAV","gene_name":"negative regulator of antiviral response (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48588]","synonyms":"DYNLL1-AS1","biotype":"antisense_RNA","ncbi_id":"100506668","summary":null,"start":120490328,"end":120495940,"strand":-1,"description":"negative regulator of antiviral response (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48588]"}, {"versioned_ensembl_gene_id":"ENSG00000263004.1","gene_symbol":"AC007114.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57078298,"end":57085024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230146.1","gene_symbol":"SEPHS1P4","gene_name":"selenophosphate synthetase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42169]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389873","summary":null,"start":73769248,"end":73770423,"strand":1,"description":"selenophosphate synthetase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42169]"}, {"versioned_ensembl_gene_id":"ENSG00000227173.1","gene_symbol":"MYL6P3","gene_name":"myosin light chain 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37812]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129561","summary":null,"start":65169438,"end":65169869,"strand":-1,"description":"myosin light chain 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37812]"}, {"versioned_ensembl_gene_id":"ENSG00000250088.1","gene_symbol":"AC233724.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17587290,"end":17587523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284465.1","gene_symbol":"AC233724.21","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17585162,"end":17585758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272603.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"NOL5B,NOP56-L,dJ207F6.1,NOL5BP","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783625,"end":28783996,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000284283.1","gene_symbol":"AC106774.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17521801,"end":17522397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100197.20","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CPD6,P450C2D,CYP2D8P2,CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP","biotype":"protein_coding","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126499,"end":42130906,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000213790.2","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107765,"end":42108953,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000248205.1","gene_symbol":"AC106774.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17502043,"end":17502363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186001.12","gene_symbol":"LRCH3","gene_name":"leucine rich repeats and calponin homology domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28637]","synonyms":"MGC4126","biotype":"protein_coding","ncbi_id":"84859","summary":null,"start":197791226,"end":197888436,"strand":1,"description":"leucine rich repeats and calponin homology domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28637]"}, {"versioned_ensembl_gene_id":"ENSG00000272908.1","gene_symbol":"AC006033.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38326070,"end":38329643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228668.1","gene_symbol":"TRGV5P","gene_name":"T-cell receptor gamma variable 5P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12291]","synonyms":"V1S5P,TCRGV5P","biotype":"TR_V_pseudogene","ncbi_id":"6979","summary":null,"start":38345030,"end":38345499,"strand":-1,"description":"T-cell receptor gamma variable 5P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12291]"}, {"versioned_ensembl_gene_id":"ENSG00000235733.2","gene_symbol":"AL024509.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25245356,"end":25261411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211695.2","gene_symbol":"TRGV9","gene_name":"T-cell receptor gamma variable 9 [Source:HGNC Symbol;Acc:HGNC:12295]","synonyms":"V2,TCRGV9","biotype":"TR_V_gene","ncbi_id":"6983","summary":null,"start":38317017,"end":38318861,"strand":-1,"description":"T-cell receptor gamma variable 9 [Source:HGNC Symbol;Acc:HGNC:12295]"}, {"versioned_ensembl_gene_id":"ENSG00000186508.4","gene_symbol":"OR9I2P","gene_name":"olfactory receptor family 9 subfamily I member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15324]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81156","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58144495,"end":58145397,"strand":1,"description":"olfactory receptor family 9 subfamily I member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15324]"}, {"versioned_ensembl_gene_id":"ENSG00000272685.1","gene_symbol":"AP004247.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58108720,"end":58109661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211697.4","gene_symbol":"TRGV5","gene_name":"T-cell receptor gamma variable 5 [Source:HGNC Symbol;Acc:HGNC:12290]","synonyms":"V1S5,TCRGV5","biotype":"TR_V_gene","ncbi_id":"6978","summary":null,"start":38349355,"end":38350022,"strand":-1,"description":"T-cell receptor gamma variable 5 [Source:HGNC Symbol;Acc:HGNC:12290]"}, {"versioned_ensembl_gene_id":"ENSG00000236541.1","gene_symbol":"VN2R9P","gene_name":"vomeronasal 2 receptor 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33215]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"648315","summary":null,"start":58040708,"end":58041660,"strand":-1,"description":"vomeronasal 2 receptor 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33215]"}, {"versioned_ensembl_gene_id":"ENSG00000211696.2","gene_symbol":"TRGV8","gene_name":"T-cell receptor gamma variable 8 [Source:HGNC Symbol;Acc:HGNC:12294]","synonyms":"V1S8,TCRGV8","biotype":"TR_V_gene","ncbi_id":"6982","summary":null,"start":38330343,"end":38330935,"strand":-1,"description":"T-cell receptor gamma variable 8 [Source:HGNC Symbol;Acc:HGNC:12294]"}, {"versioned_ensembl_gene_id":"ENSG00000112038.17","gene_symbol":"OPRM1","gene_name":"opioid receptor mu 1 [Source:HGNC Symbol;Acc:HGNC:8156]","synonyms":"MOR1","biotype":"protein_coding","ncbi_id":"4988","summary":"This gene encodes one of at least three opioid receptors in humans; the mu opioid receptor (MOR). The MOR is the principal target of endogenous opioid peptides and opioid analgesic agents such as beta-endorphin and enkephalins. The MOR also has an important role in dependence to other drugs of abuse, such as nicotine, cocaine, and alcohol via its modulation of the dopamine system. The NM_001008503.2:c.118A>G allele has been associated with opioid and alcohol addiction and variations in pain sensitivity but evidence for it having a causal role is conflicting. Multiple transcript variants encoding different isoforms have been found for this gene. Though the canonical MOR belongs to the superfamily of 7-transmembrane-spanning G-protein-coupled receptors some isoforms of this gene have only 6 transmembrane domains. [provided by RefSeq, Oct 2013]","start":154010496,"end":154246867,"strand":1,"description":"opioid receptor mu 1 [Source:HGNC Symbol;Acc:HGNC:8156]"}, {"versioned_ensembl_gene_id":"ENSG00000259360.1","gene_symbol":"AC009558.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47397501,"end":47399554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164128.6","gene_symbol":"NPY1R","gene_name":"neuropeptide Y receptor Y1 [Source:HGNC Symbol;Acc:HGNC:7956]","synonyms":"NPYR","biotype":"protein_coding","ncbi_id":"4886","summary":"This gene belongs to the G-protein-coupled receptor superfamily. The encoded transmembrane protein mediates the function of neuropeptide Y (NPY), a neurotransmitter, and peptide YY (PYY), a gastrointestinal hormone. The encoded receptor undergoes fast agonist-induced internalization through clathrin-coated pits and is subsequently recycled back to the cell membrane. Activation of Y1 receptors may result in mobilization of intracellular calcium and inhibition of adenylate cyclase activity. [provided by RefSeq, Aug 2013]","start":163323961,"end":163344832,"strand":-1,"description":"neuropeptide Y receptor Y1 [Source:HGNC Symbol;Acc:HGNC:7956]"}, {"versioned_ensembl_gene_id":"ENSG00000261080.1","gene_symbol":"RUNX2-AS1","gene_name":"RUNX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53512]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105375077","summary":null,"start":45573346,"end":45576770,"strand":-1,"description":"RUNX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53512]"}, {"versioned_ensembl_gene_id":"ENSG00000259588.1","gene_symbol":"AC012050.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47603880,"end":47606352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228566.1","gene_symbol":"AC022387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63664664,"end":63990568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282950.1","gene_symbol":"AC063952.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120365993,"end":120368326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213609.3","gene_symbol":"RPL7AP50","gene_name":"ribosomal protein L7a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"87688","summary":null,"start":63902451,"end":63903245,"strand":-1,"description":"ribosomal protein L7a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36117]"}, {"versioned_ensembl_gene_id":"ENSG00000270352.1","gene_symbol":"AC022387.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63658074,"end":63658521,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257634.1","gene_symbol":"AC079310.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54682973,"end":54687434,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260918.1","gene_symbol":"AC107398.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":47431960,"end":47438959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232957.11","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-D0-alpha,HLA-DZA,HLA-DNA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":33144838,"end":33150271,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000232075.1","gene_symbol":"MRPL35P2","gene_name":"mitochondrial ribosomal protein L35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29706]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359743","summary":null,"start":63634317,"end":63634827,"strand":-1,"description":"mitochondrial ribosomal protein L35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29706]"}, {"versioned_ensembl_gene_id":"ENSG00000270611.1","gene_symbol":"AC006363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9850924,"end":9851386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238180.1","gene_symbol":"AC017079.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128217588,"end":128218072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221994.10","gene_symbol":"ZNF630","gene_name":"zinc finger protein 630 [Source:HGNC Symbol;Acc:HGNC:28855]","synonyms":"dJ54B20.2,BC037316,MGC138344,FLJ20573","biotype":"protein_coding","ncbi_id":"57232","summary":"This gene encodes a protein containing an N-terminal Kruppel-associated box-containing (KRAB) domain and 13 Kruppel-type C2H2 zinc finger domains. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":47983356,"end":48071658,"strand":-1,"description":"zinc finger protein 630 [Source:HGNC Symbol;Acc:HGNC:28855]"}, {"versioned_ensembl_gene_id":"ENSG00000181827.14","gene_symbol":"RFX7","gene_name":"regulatory factor X7 [Source:HGNC Symbol;Acc:HGNC:25777]","synonyms":"RFXDC2,FLJ12994","biotype":"protein_coding","ncbi_id":"64864","summary":"RFX7 is a member of the regulatory factor X (RFX) family of transcription factors (see RFX1, MIM 600006) (Aftab et al., 2008 [PubMed 18673564]).[supplied by OMIM, Mar 2009]","start":56087280,"end":56243266,"strand":-1,"description":"regulatory factor X7 [Source:HGNC Symbol;Acc:HGNC:25777]"}, {"versioned_ensembl_gene_id":"ENSG00000241179.1","gene_symbol":"AC010301.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134804778,"end":134805132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114473.13","gene_symbol":"IQCG","gene_name":"IQ motif containing G [Source:HGNC Symbol;Acc:HGNC:25251]","synonyms":"DRC9,DKFZp434B227,CFAP122","biotype":"protein_coding","ncbi_id":"84223","summary":null,"start":197889075,"end":197960142,"strand":-1,"description":"IQ motif containing G [Source:HGNC Symbol;Acc:HGNC:25251]"}, {"versioned_ensembl_gene_id":"ENSG00000276449.1","gene_symbol":"AC004076.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57449689,"end":57453011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170165.5","gene_symbol":"CR848007.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42901238,"end":42920095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236816.2","gene_symbol":"ANKRD20A7P","gene_name":"ankyrin repeat domain 20 family member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31980]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653436","summary":null,"start":42852675,"end":42894751,"strand":1,"description":"ankyrin repeat domain 20 family member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:31980]"}, {"versioned_ensembl_gene_id":"ENSG00000272461.1","gene_symbol":"AP005328.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":962592,"end":976883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145833.15","gene_symbol":"DDX46","gene_name":"DEAD-box helicase 46 [Source:HGNC Symbol;Acc:HGNC:18681]","synonyms":"PRPF5,Prp5,KIAA0801,FLJ25329","biotype":"protein_coding","ncbi_id":"9879","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a component of the 17S U2 snRNP complex; it plays an important role in pre-mRNA splicing. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2014]","start":134758771,"end":134855133,"strand":1,"description":"DEAD-box helicase 46 [Source:HGNC Symbol;Acc:HGNC:18681]"}, {"versioned_ensembl_gene_id":"ENSG00000149527.17","gene_symbol":"PLCH2","gene_name":"phospholipase C eta 2 [Source:HGNC Symbol;Acc:HGNC:29037]","synonyms":"PLC-eta2,KIAA0450,RP3-395M20.1,PLCL4,PLCeta2","biotype":"protein_coding","ncbi_id":"9651","summary":"PLCH2 is a member of the PLC-eta family of the phosphoinositide-specific phospholipase C (PLC) superfamily of enzymes that cleave PtdIns(4,5) P2 to generate second messengers inositol 1,4,5-trisphosphate and diacylglycerol (Zhou et al., 2005 [PubMed 16107206]).[supplied by OMIM, Jun 2009]","start":2425980,"end":2505530,"strand":1,"description":"phospholipase C eta 2 [Source:HGNC Symbol;Acc:HGNC:29037]"}, {"versioned_ensembl_gene_id":"ENSG00000206306.10","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32513411,"end":32544028,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000228041.2","gene_symbol":"AL031313.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82497669,"end":82497924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233446.2","gene_symbol":"AL691517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81600072,"end":81601306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235264.1","gene_symbol":"RPL5P28","gene_name":"ribosomal protein L5 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36827]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131535","summary":null,"start":133144612,"end":133145304,"strand":-1,"description":"ribosomal protein L5 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36827]"}, {"versioned_ensembl_gene_id":"ENSG00000264622.1","gene_symbol":"AC022903.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34837871,"end":34859046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264174.1","gene_symbol":"AC005552.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34725509,"end":34726170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247934.4","gene_symbol":"AC022364.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28163298,"end":28190738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154832.14","gene_symbol":"CXXC1","gene_name":"CXXC finger protein 1 [Source:HGNC Symbol;Acc:HGNC:24343]","synonyms":"ZCGPC1,SPP1,PHF18,PCCX1,HsT2645,hCGBP,CGBP,CFP1","biotype":"protein_coding","ncbi_id":"30827","summary":"This gene encodes a protein that functions as a transcriptional activator that binds specifically to non-methylated CpG motifs through its CXXC domain. The protein is a component of the SETD1 complex, regulates gene expression and is essential for vertebrate development. [provided by RefSeq, Sep 2015]","start":50282343,"end":50288304,"strand":-1,"description":"CXXC finger protein 1 [Source:HGNC Symbol;Acc:HGNC:24343]"}, {"versioned_ensembl_gene_id":"ENSG00000272980.4","gene_symbol":"Z94721.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":166999405,"end":167139141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230592.2","gene_symbol":"RPSAP8","gene_name":"ribosomal protein SA pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31462]","synonyms":"LAMR1P8","biotype":"processed_pseudogene","ncbi_id":"643617","summary":null,"start":100155885,"end":100156773,"strand":-1,"description":"ribosomal protein SA pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31462]"}, {"versioned_ensembl_gene_id":"ENSG00000155970.11","gene_symbol":"MICU3","gene_name":"mitochondrial calcium uptake family member 3 [Source:HGNC Symbol;Acc:HGNC:27820]","synonyms":"EFHA2,DKFZp313A0139","biotype":"protein_coding","ncbi_id":"286097","summary":null,"start":17027238,"end":17122644,"strand":1,"description":"mitochondrial calcium uptake family member 3 [Source:HGNC Symbol;Acc:HGNC:27820]"}, {"versioned_ensembl_gene_id":"ENSG00000233128.1","gene_symbol":"LINC01794","gene_name":"long intergenic non-protein coding RNA 1794 [Source:HGNC Symbol;Acc:HGNC:52584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929700","summary":null,"start":40746487,"end":40767452,"strand":1,"description":"long intergenic non-protein coding RNA 1794 [Source:HGNC Symbol;Acc:HGNC:52584]"}, {"versioned_ensembl_gene_id":"ENSG00000268295.1","gene_symbol":"POLR3GP1","gene_name":"RNA polymerase III subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23345]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100422395","summary":null,"start":91603173,"end":91603433,"strand":-1,"description":"RNA polymerase III subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23345]"}, {"versioned_ensembl_gene_id":"ENSG00000241397.1","gene_symbol":"LINC00903","gene_name":"long intergenic non-protein coding RNA 903 [Source:HGNC Symbol;Acc:HGNC:40351]","synonyms":"LSAMP-AS2","biotype":"antisense_RNA","ncbi_id":"100861506","summary":null,"start":116552473,"end":116568264,"strand":1,"description":"long intergenic non-protein coding RNA 903 [Source:HGNC Symbol;Acc:HGNC:40351]"}, {"versioned_ensembl_gene_id":"ENSG00000237773.5","gene_symbol":"AC003075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17279834,"end":17299357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218857.1","gene_symbol":"AL137222.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131184325,"end":131185486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267197.1","gene_symbol":"AC011461.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":10490339,"end":10491000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266100.1","gene_symbol":"AC007431.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57522248,"end":57523597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000020426.10","gene_symbol":"MNAT1","gene_name":"MNAT1, CDK activating kinase assembly factor [Source:HGNC Symbol;Acc:HGNC:7181]","synonyms":"RNF66,MAT1","biotype":"protein_coding","ncbi_id":"4331","summary":"The protein encoded by this gene, along with cyclin H and CDK7, forms the CDK-activating kinase (CAK) enzymatic complex. This complex activates several cyclin-associated kinases and can also associate with TFIIH to activate transcription by RNA polymerase II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":60734742,"end":60969953,"strand":1,"description":"MNAT1, CDK activating kinase assembly factor [Source:HGNC Symbol;Acc:HGNC:7181]"}, {"versioned_ensembl_gene_id":"ENSG00000279281.1","gene_symbol":"AC015883.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57448218,"end":57450291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263499.1","gene_symbol":"AC007431.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57600856,"end":57608412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091844.7","gene_symbol":"RGS17","gene_name":"regulator of G protein signaling 17 [Source:HGNC Symbol;Acc:HGNC:14088]","synonyms":"RGSZ2,RGS-17","biotype":"protein_coding","ncbi_id":"26575","summary":"This gene encodes a member of the regulator of G-protein signaling family. This protein contains a conserved, 120 amino acid motif called the RGS domain and a cysteine-rich region. The protein attenuates the signaling activity of G-proteins by binding to activated, GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal. [provided by RefSeq, Jul 2008]","start":153004459,"end":153131249,"strand":-1,"description":"regulator of G protein signaling 17 [Source:HGNC Symbol;Acc:HGNC:14088]"}, {"versioned_ensembl_gene_id":"ENSG00000136925.14","gene_symbol":"TSTD2","gene_name":"thiosulfate sulfurtransferase like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30087]","synonyms":"PP4189,C9orf97","biotype":"protein_coding","ncbi_id":"158427","summary":null,"start":97600080,"end":97633575,"strand":-1,"description":"thiosulfate sulfurtransferase like domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30087]"}, {"versioned_ensembl_gene_id":"ENSG00000231521.1","gene_symbol":"AL162385.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97634515,"end":97636051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185220.11","gene_symbol":"PGBD2","gene_name":"piggyBac transposable element derived 2 [Source:HGNC Symbol;Acc:HGNC:19399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"267002","summary":"The piggyBac family of proteins, found in diverse animals, are transposases related to the transposase of the canonical piggyBac transposon from the moth, Trichoplusia ni. This family also includes genes in several genomes, including human, that appear to have been derived from the piggyBac transposons. This gene belongs to the subfamily of piggyBac transposable element derived (PGBD) genes. The PGBD proteins appear to be novel, with no obvious relationship to other transposases, or other known protein families. The exact function of this gene is not known. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":248906196,"end":248919946,"strand":1,"description":"piggyBac transposable element derived 2 [Source:HGNC Symbol;Acc:HGNC:19399]"}, {"versioned_ensembl_gene_id":"ENSG00000227237.1","gene_symbol":"AL672291.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":248859164,"end":248864796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247271.6","gene_symbol":"ZBED5-AS1","gene_name":"ZBED5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48646]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729013","summary":null,"start":10858259,"end":10906802,"strand":1,"description":"ZBED5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48646]"}, {"versioned_ensembl_gene_id":"ENSG00000226035.2","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32417316,"end":32430998,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000267328.1","gene_symbol":"AC002398.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35754566,"end":35755490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229522.1","gene_symbol":"LINC01523","gene_name":"long intergenic non-protein coding RNA 1523 [Source:HGNC Symbol;Acc:HGNC:51225]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060004","summary":null,"start":47983404,"end":47984313,"strand":1,"description":"long intergenic non-protein coding RNA 1523 [Source:HGNC Symbol;Acc:HGNC:51225]"}, {"versioned_ensembl_gene_id":"ENSG00000237423.1","gene_symbol":"LINC01522","gene_name":"long intergenic non-protein coding RNA 1522 [Source:HGNC Symbol;Acc:HGNC:51224]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927457","summary":null,"start":47980488,"end":47988744,"strand":-1,"description":"long intergenic non-protein coding RNA 1522 [Source:HGNC Symbol;Acc:HGNC:51224]"}, {"versioned_ensembl_gene_id":"ENSG00000100290.2","gene_symbol":"BIK","gene_name":"BCL2 interacting killer [Source:HGNC Symbol;Acc:HGNC:1051]","synonyms":"NBK","biotype":"protein_coding","ncbi_id":"638","summary":"The protein encoded by this gene shares a critical BH3 domain with other death-promoting proteins, such as BID, BAK, BAD and BAX, that is required for its pro-apoptotic activity, and for interaction with anti-apoptotic members of the BCL2 family, and viral survival-promoting proteins. Since the activity of this protein is suppressed in the presence of survival-promoting proteins, it is suggested as a likely target for anti-apoptotic proteins. [provided by RefSeq, Sep 2011]","start":43110748,"end":43129712,"strand":1,"description":"BCL2 interacting killer [Source:HGNC Symbol;Acc:HGNC:1051]"}, {"versioned_ensembl_gene_id":"ENSG00000234967.1","gene_symbol":"AL357558.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47950799,"end":47952055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241961.1","gene_symbol":"AC011037.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67406515,"end":67407072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229613.1","gene_symbol":"LINC01501","gene_name":"long intergenic non-protein coding RNA 1501 [Source:HGNC Symbol;Acc:HGNC:27988]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340515","summary":null,"start":90463524,"end":90582744,"strand":-1,"description":"long intergenic non-protein coding RNA 1501 [Source:HGNC Symbol;Acc:HGNC:27988]"}, {"versioned_ensembl_gene_id":"ENSG00000182095.14","gene_symbol":"TNRC18","gene_name":"trinucleotide repeat containing 18 [Source:HGNC Symbol;Acc:HGNC:11962]","synonyms":"TNRC18A,KIAA1856,CAGL79","biotype":"protein_coding","ncbi_id":"84629","summary":null,"start":5306790,"end":5425414,"strand":-1,"description":"trinucleotide repeat containing 18 [Source:HGNC Symbol;Acc:HGNC:11962]"}, {"versioned_ensembl_gene_id":"ENSG00000241269.1","gene_symbol":"AC093620.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5419827,"end":5420767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258386.1","gene_symbol":"AL352984.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32006902,"end":32018685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279503.1","gene_symbol":"AL353649.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90158028,"end":90158646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268736.1","gene_symbol":"MTCO3P39","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52142]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075313","summary":null,"start":49246021,"end":49246538,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52142]"}, {"versioned_ensembl_gene_id":"ENSG00000278942.1","gene_symbol":"AC004494.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3533429,"end":3534258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215811.6","gene_symbol":"BTNL10","gene_name":"butyrophilin like 10 [Source:HGNC Symbol;Acc:HGNC:42540]","synonyms":"BUTR1,BTN4","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100129094","summary":null,"start":228510425,"end":228512305,"strand":-1,"description":"butyrophilin like 10 [Source:HGNC Symbol;Acc:HGNC:42540]"}, {"versioned_ensembl_gene_id":"ENSG00000143429.10","gene_symbol":"AC116050.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91617160,"end":91659972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129467.13","gene_symbol":"ADCY4","gene_name":"adenylate cyclase 4 [Source:HGNC Symbol;Acc:HGNC:235]","synonyms":"AC4","biotype":"protein_coding","ncbi_id":"196883","summary":"This gene encodes a member of the family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). Mouse studies show that adenylate cyclase 4, along with adenylate cyclases 2 and 3, is expressed in olfactory cilia, suggesting that several different adenylate cyclases may couple to olfactory receptors and that there may be multiple receptor-mediated mechanisms for the generation of cAMP signals. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010]","start":24318349,"end":24335093,"strand":-1,"description":"adenylate cyclase 4 [Source:HGNC Symbol;Acc:HGNC:235]"}, {"versioned_ensembl_gene_id":"ENSG00000227555.1","gene_symbol":"MIR4290HG","gene_name":"MIR4290 host gene [Source:HGNC Symbol;Acc:HGNC:27861]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286370","summary":null,"start":90020654,"end":90041499,"strand":-1,"description":"MIR4290 host gene [Source:HGNC Symbol;Acc:HGNC:27861]"}, {"versioned_ensembl_gene_id":"ENSG00000134668.12","gene_symbol":"SPOCD1","gene_name":"SPOC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26338]","synonyms":"PPP1R146,FLJ25348","biotype":"protein_coding","ncbi_id":"90853","summary":"This gene encodes a protein that belongs to the TFIIS family of transcription factors. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":31790422,"end":31816051,"strand":-1,"description":"SPOC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26338]"}, {"versioned_ensembl_gene_id":"ENSG00000261972.5","gene_symbol":"CES5A","gene_name":"carboxylesterase 5A [Source:HGNC Symbol;Acc:HGNC:26459]","synonyms":"FLJ31547,CES7,CES5,CES4C1,CAUXIN","biotype":"protein_coding","ncbi_id":"221223","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They also participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene, also called CES5, is predominantly expressed in peripheral tissues, including brain, kidney, lung and testis. It encodes a secreted enzyme. Because of high levels in the urine of male domestic cats, this enzyme is also called cauxin (carboxylesterase-like urinary excreted protein). The enzyme functions in regulating the production of a pheromone precursor and may contribute to lipid and cholesterol transfer processes within male reproductive fluids. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":55843031,"end":55952925,"strand":-1,"description":"carboxylesterase 5A [Source:HGNC Symbol;Acc:HGNC:26459]"}, {"versioned_ensembl_gene_id":"ENSG00000182271.12","gene_symbol":"TMIGD1","gene_name":"transmembrane and immunoglobulin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32431]","synonyms":"UNQ9372,TMIGD","biotype":"protein_coding","ncbi_id":"388364","summary":null,"start":30316333,"end":30334059,"strand":-1,"description":"transmembrane and immunoglobulin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32431]"}, {"versioned_ensembl_gene_id":"ENSG00000257365.7","gene_symbol":"FNTB","gene_name":"farnesyltransferase, CAAX box, beta [Source:HGNC Symbol;Acc:HGNC:3785]","synonyms":"FPTB","biotype":"protein_coding","ncbi_id":"2342","summary":null,"start":64986720,"end":65062652,"strand":1,"description":"farnesyltransferase, CAAX box, beta [Source:HGNC Symbol;Acc:HGNC:3785]"}, {"versioned_ensembl_gene_id":"ENSG00000215712.10","gene_symbol":"TMEM242","gene_name":"transmembrane protein 242 [Source:HGNC Symbol;Acc:HGNC:17206]","synonyms":"C6orf35,BM033","biotype":"protein_coding","ncbi_id":"729515","summary":null,"start":157289386,"end":157323601,"strand":-1,"description":"transmembrane protein 242 [Source:HGNC Symbol;Acc:HGNC:17206]"}, {"versioned_ensembl_gene_id":"ENSG00000156858.11","gene_symbol":"PRR14","gene_name":"proline rich 14 [Source:HGNC Symbol;Acc:HGNC:28458]","synonyms":"MGC3121","biotype":"protein_coding","ncbi_id":"78994","summary":"The protein encoded by this gene tethers heterochromatin to the nuclear laminar scaffold by binding heterochromatin protein 1 (HP1) and the nuclear lamina. The tether is broken during mitosis and reforms quickly after mitosis, with the encoded protein first binding HP1 and then attaching to the nuclear lamina. This protein also has been shown to promote MyoD activity and skeletal myogenesis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2016]","start":30650717,"end":30656440,"strand":1,"description":"proline rich 14 [Source:HGNC Symbol;Acc:HGNC:28458]"}, {"versioned_ensembl_gene_id":"ENSG00000271040.1","gene_symbol":"AL390955.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157323964,"end":157324477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161800.12","gene_symbol":"RACGAP1","gene_name":"Rac GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:9804]","synonyms":"MgcRacGAP","biotype":"protein_coding","ncbi_id":"29127","summary":"This gene encodes a GTPase-activating protein (GAP) that is a compoment of the centralspindlin complex. This protein binds activated forms of Rho GTPases and stimulates GTP hydrolysis, which results in negative regulation of Rho-mediated signals. This protein plays a regulatory role in cytokinesis, cell growth, and differentiation. Alternatively spliced transcript variants have been found for this gene. There is a pseudogene for this gene on chromosome 12. [provided by RefSeq, Feb 2016]","start":49976923,"end":50033136,"strand":-1,"description":"Rac GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:9804]"}, {"versioned_ensembl_gene_id":"ENSG00000282283.1","gene_symbol":"PLPPR3","gene_name":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]","synonyms":"LPPR3,FLJ11535,PRG2,PRG-2","biotype":"protein_coding","ncbi_id":"79948","summary":"The proteins in the lipid phosphate phosphatase (LPP) family, including PRG2, are integral membrane proteins that modulate bioactive lipid phosphates including phosphatidate, lysophosphatidate, and sphingosine-1-phosphate in the context of cell migration, neurite retraction, and mitogenesis (Brauer et al., 2003 [PubMed 12730698]).[supplied by OMIM, Mar 2008]","start":821485,"end":821977,"strand":-1,"description":"phospholipid phosphatase related 3 [Source:HGNC Symbol;Acc:HGNC:23497]"}, {"versioned_ensembl_gene_id":"ENSG00000170983.3","gene_symbol":"LINC00208","gene_name":"long intergenic non-protein coding RNA 208 [Source:HGNC Symbol;Acc:HGNC:15535]","synonyms":"NCRNA00208,C8orf14","biotype":"lincRNA","ncbi_id":"83655","summary":null,"start":11576313,"end":11581342,"strand":1,"description":"long intergenic non-protein coding RNA 208 [Source:HGNC Symbol;Acc:HGNC:15535]"}, {"versioned_ensembl_gene_id":"ENSG00000164929.16","gene_symbol":"BAALC","gene_name":"BAALC, MAP3K1 and KLF4 binding [Source:HGNC Symbol;Acc:HGNC:14333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79870","summary":"This gene was identified by gene expression studies in patients with acute myeloid leukemia (AML). The gene is conserved among mammals and is not found in lower organisms. Tissues that express this gene develop from the neuroectoderm. Multiple alternatively spliced transcript variants that encode different proteins have been described for this gene; however, some of the transcript variants are found only in AML cell lines. [provided by RefSeq, Jul 2008]","start":103140710,"end":103230305,"strand":1,"description":"BAALC, MAP3K1 and KLF4 binding [Source:HGNC Symbol;Acc:HGNC:14333]"}, {"versioned_ensembl_gene_id":"ENSG00000223927.1","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31270107,"end":31271306,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000262151.1","gene_symbol":"AC133065.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10864914,"end":10888752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133105.7","gene_symbol":"RXFP2","gene_name":"relaxin/insulin like family peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:17318]","synonyms":"RXFPR2,LGR8,INSL3R,GREAT,GPR106","biotype":"protein_coding","ncbi_id":"122042","summary":"This gene encodes a member of the GPCR (G protein-coupled, 7-transmembrane receptor) family. Mutations in this gene are associated with cryptorchidism. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":31739542,"end":31803388,"strand":1,"description":"relaxin/insulin like family peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:17318]"}, {"versioned_ensembl_gene_id":"ENSG00000186439.12","gene_symbol":"TRDN","gene_name":"triadin [Source:HGNC Symbol;Acc:HGNC:12261]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10345","summary":"This gene encodes an integral membrane protein that contains a single transmembrane domain. As similar protein in rabbits plays a role in skeletal muscle excitation-contraction coupling as part of the calcium release complex in association with the ryanodine receptor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and single nucleotide polymorphisms in this gene may be markers for IgA nephritis. [provided by RefSeq, Oct 2011]","start":123216339,"end":123637093,"strand":-1,"description":"triadin [Source:HGNC Symbol;Acc:HGNC:12261]"}, {"versioned_ensembl_gene_id":"ENSG00000134443.9","gene_symbol":"GRP","gene_name":"gastrin releasing peptide [Source:HGNC Symbol;Acc:HGNC:4605]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2922","summary":"This gene encodes a member of the bombesin-like family of gastrin-releasing peptides. The encoded preproprotein is proteolytically processed to generate two peptides, gastrin-releasing peptide and neuromedin-C. These peptides regulate numerous functions of the gastrointestinal and central nervous systems, including release of gastrointestinal hormones, smooth muscle cell contraction, and epithelial cell proliferation. These peptides are also likely to play a role in human cancers of the lung, colon, stomach, pancreas, breast, and prostate. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":59220168,"end":59230774,"strand":1,"description":"gastrin releasing peptide [Source:HGNC Symbol;Acc:HGNC:4605]"}, {"versioned_ensembl_gene_id":"ENSG00000270661.1","gene_symbol":"Z99289.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112217640,"end":112219570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157103.10","gene_symbol":"SLC6A1","gene_name":"solute carrier family 6 member 1 [Source:HGNC Symbol;Acc:HGNC:11042]","synonyms":"GABATR,GABATHG,GAT1","biotype":"protein_coding","ncbi_id":"6529","summary":"The protein encoded by this gene is a gamma-aminobutyric acid (GABA) transporter that localizes to the plasma membrane. The encoded protein removes GABA from the synaptic cleft, restoring it to presynaptic terminals. [provided by RefSeq, Jan 2017]","start":10992724,"end":11039247,"strand":1,"description":"solute carrier family 6 member 1 [Source:HGNC Symbol;Acc:HGNC:11042]"}, {"versioned_ensembl_gene_id":"ENSG00000271208.1","gene_symbol":"Z99289.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112234165,"end":112234758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127824.13","gene_symbol":"TUBA4A","gene_name":"tubulin alpha 4a [Source:HGNC Symbol;Acc:HGNC:12407]","synonyms":"TUBA1,H2-ALPHA,FLJ30169","biotype":"protein_coding","ncbi_id":"7277","summary":"Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulin. The genes encoding these microtubule constituents are part of the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes and they are highly conserved among and between species. This gene encodes an alpha tubulin that is a highly conserved homolog of a rat testis-specific alpha tubulin. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]","start":219249711,"end":219278170,"strand":-1,"description":"tubulin alpha 4a [Source:HGNC Symbol;Acc:HGNC:12407]"}, {"versioned_ensembl_gene_id":"ENSG00000157343.8","gene_symbol":"ARMC12","gene_name":"armadillo repeat containing 12 [Source:HGNC Symbol;Acc:HGNC:21099]","synonyms":"FLJ25390,C6orf81","biotype":"protein_coding","ncbi_id":"221481","summary":null,"start":35737032,"end":35749079,"strand":1,"description":"armadillo repeat containing 12 [Source:HGNC Symbol;Acc:HGNC:21099]"}, {"versioned_ensembl_gene_id":"ENSG00000204528.3","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"sense_intronic","ncbi_id":"100130889","summary":null,"start":31173735,"end":31177899,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000175874.9","gene_symbol":"CREG2","gene_name":"cellular repressor of E1A stimulated genes 2 [Source:HGNC Symbol;Acc:HGNC:14272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200407","summary":null,"start":101345551,"end":101387595,"strand":-1,"description":"cellular repressor of E1A stimulated genes 2 [Source:HGNC Symbol;Acc:HGNC:14272]"}, {"versioned_ensembl_gene_id":"ENSG00000279571.3","gene_symbol":"AL162426.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127690098,"end":127690840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141946.1","gene_symbol":"ZIM3","gene_name":"zinc finger imprinted 3 [Source:HGNC Symbol;Acc:HGNC:16366]","synonyms":"ZNF657","biotype":"protein_coding","ncbi_id":"114026","summary":null,"start":57134096,"end":57145202,"strand":-1,"description":"zinc finger imprinted 3 [Source:HGNC Symbol;Acc:HGNC:16366]"}, {"versioned_ensembl_gene_id":"ENSG00000282886.1","gene_symbol":"AL691447.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94347234,"end":94347563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232063.1","gene_symbol":"AL691447.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94332476,"end":94360948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230990.1","gene_symbol":"AL049649.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11234170,"end":11301525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187268.11","gene_symbol":"FAM9C","gene_name":"family with sequence similarity 9 member C [Source:HGNC Symbol;Acc:HGNC:18405]","synonyms":"TEX39C","biotype":"protein_coding","ncbi_id":"171484","summary":"This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex protein. [provided by RefSeq, Aug 2011]","start":13035618,"end":13044682,"strand":-1,"description":"family with sequence similarity 9 member C [Source:HGNC Symbol;Acc:HGNC:18405]"}, {"versioned_ensembl_gene_id":"ENSG00000125899.7","gene_symbol":"C20orf187","gene_name":"chromosome 20 open reading frame 187 [Source:HGNC Symbol;Acc:HGNC:16180]","synonyms":"dJ727I10.1","biotype":"lincRNA","ncbi_id":"728434","summary":null,"start":11027760,"end":11029366,"strand":1,"description":"chromosome 20 open reading frame 187 [Source:HGNC Symbol;Acc:HGNC:16180]"}, {"versioned_ensembl_gene_id":"ENSG00000250938.5","gene_symbol":"AC108866.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120066958,"end":120416766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254236.1","gene_symbol":"AP003550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103020187,"end":103021428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282186.1","gene_symbol":"IGHVII-74-1","gene_name":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]","synonyms":"IGHV(II)-74-1","biotype":"IG_V_pseudogene","ncbi_id":"28357","summary":null,"start":106845350,"end":106845590,"strand":-1,"description":"immunoglobulin heavy variable (II)-74-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5690]"}, {"versioned_ensembl_gene_id":"ENSG00000216762.1","gene_symbol":"VN1R13P","gene_name":"vomeronasal 1 receptor 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:18723]","synonyms":"VNR6I4P,hs6V1-4p,bA373D17.3","biotype":"processed_pseudogene","ncbi_id":"387322","summary":null,"start":27060365,"end":27061249,"strand":-1,"description":"vomeronasal 1 receptor 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:18723]"}, {"versioned_ensembl_gene_id":"ENSG00000234017.1","gene_symbol":"AC022018.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112548632,"end":112548872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163521.15","gene_symbol":"GLB1L","gene_name":"galactosidase beta 1 like [Source:HGNC Symbol;Acc:HGNC:28129]","synonyms":"MGC10771","biotype":"protein_coding","ncbi_id":"79411","summary":null,"start":219236606,"end":219245478,"strand":-1,"description":"galactosidase beta 1 like [Source:HGNC Symbol;Acc:HGNC:28129]"}, {"versioned_ensembl_gene_id":"ENSG00000262243.5","gene_symbol":"CES1","gene_name":"carboxylesterase 1 [Source:HGNC Symbol;Acc:HGNC:1863]","synonyms":"HMSE,CES2,CES1A2,CES1A1,CEH,SES1,HMSE1","biotype":"protein_coding","ncbi_id":"1066","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This enzyme is the major liver enzyme and functions in liver drug clearance. Mutations of this gene cause carboxylesterase 1 deficiency. Three transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":55799704,"end":55830035,"strand":-1,"description":"carboxylesterase 1 [Source:HGNC Symbol;Acc:HGNC:1863]"}, {"versioned_ensembl_gene_id":"ENSG00000279735.2","gene_symbol":"AC124312.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25091960,"end":25092377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280234.1","gene_symbol":"AC124303.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25255579,"end":25257027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151834.15","gene_symbol":"GABRA2","gene_name":"gamma-aminobutyric acid type A receptor alpha2 subunit [Source:HGNC Symbol;Acc:HGNC:4076]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2555","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":46248427,"end":46475230,"strand":-1,"description":"gamma-aminobutyric acid type A receptor alpha2 subunit [Source:HGNC Symbol;Acc:HGNC:4076]"}, {"versioned_ensembl_gene_id":"ENSG00000267193.5","gene_symbol":"AC023421.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45669367,"end":45747215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274353.1","gene_symbol":"AC103564.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131821987,"end":131822920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232101.1","gene_symbol":"AC108059.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128151154,"end":128151304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226392.1","gene_symbol":"MTATP6P21","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52177]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075299","summary":null,"start":67627831,"end":67628019,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52177]"}, {"versioned_ensembl_gene_id":"ENSG00000273448.1","gene_symbol":"AC006480.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67333047,"end":67334383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255154.7","gene_symbol":"HTD2","gene_name":"hydroxyacyl-thioester dehydratase type 2 [Source:HGNC Symbol;Acc:HGNC:53111]","synonyms":null,"biotype":"protein_coding","ncbi_id":"109703458","summary":"This gene encodes a protein that localizes to the mitochondria and can function as a 3-hydroxyacyl thioester dehydratase. This gene is located just downstream of the gene for ribonuclease P/MRP subunit p14 (RPP14) in a genomic context that is conserved among animals. The upstream RPP14 gene is thought to be co-transcribed with this gene, and bicistronic transcripts may include open reading frames for both proteins. [provided by RefSeq, May 2017]","start":58306262,"end":58318574,"strand":1,"description":"hydroxyacyl-thioester dehydratase type 2 [Source:HGNC Symbol;Acc:HGNC:53111]"}, {"versioned_ensembl_gene_id":"ENSG00000214530.8","gene_symbol":"STARD10","gene_name":"StAR related lipid transfer domain containing 10 [Source:HGNC Symbol;Acc:HGNC:10666]","synonyms":"SDCCAG28,PCTP2,NY-CO-28,CGI-52","biotype":"protein_coding","ncbi_id":"10809","summary":null,"start":72754729,"end":72794168,"strand":-1,"description":"StAR related lipid transfer domain containing 10 [Source:HGNC Symbol;Acc:HGNC:10666]"}, {"versioned_ensembl_gene_id":"ENSG00000215347.3","gene_symbol":"SLC25A5P1","gene_name":"solute carrier family 25 member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19250]","synonyms":"bK250D10.4,ANTP3","biotype":"processed_pseudogene","ncbi_id":"266623","summary":null,"start":42001069,"end":42001966,"strand":-1,"description":"solute carrier family 25 member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19250]"}, {"versioned_ensembl_gene_id":"ENSG00000080854.14","gene_symbol":"IGSF9B","gene_name":"immunoglobulin superfamily member 9B [Source:HGNC Symbol;Acc:HGNC:32326]","synonyms":"KIAA1030","biotype":"protein_coding","ncbi_id":"22997","summary":null,"start":133908564,"end":133956985,"strand":-1,"description":"immunoglobulin superfamily member 9B [Source:HGNC Symbol;Acc:HGNC:32326]"}, {"versioned_ensembl_gene_id":"ENSG00000254905.1","gene_symbol":"AP001318.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126292922,"end":126294254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280237.3","gene_symbol":"MIR4697HG","gene_name":"MIR4697 host gene [Source:HGNC Symbol;Acc:HGNC:27448]","synonyms":"LINC00947","biotype":"TEC","ncbi_id":"283174","summary":null,"start":133896438,"end":133901601,"strand":-1,"description":"MIR4697 host gene [Source:HGNC Symbol;Acc:HGNC:27448]"}, {"versioned_ensembl_gene_id":"ENSG00000114757.18","gene_symbol":"PEX5L","gene_name":"peroxisomal biogenesis factor 5 like [Source:HGNC Symbol;Acc:HGNC:30024]","synonyms":"TRIP8b,PXR2,PEX5R","biotype":"protein_coding","ncbi_id":"51555","summary":null,"start":179794958,"end":180037053,"strand":-1,"description":"peroxisomal biogenesis factor 5 like [Source:HGNC Symbol;Acc:HGNC:30024]"}, {"versioned_ensembl_gene_id":"ENSG00000253460.2","gene_symbol":"IGKV2OR22-3","gene_name":"immunoglobulin kappa variable 2/OR22-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5812]","synonyms":"IGKVP4,IGKV2/OR22-3","biotype":"IG_V_pseudogene","ncbi_id":"3529","summary":null,"start":16921443,"end":16922173,"strand":-1,"description":"immunoglobulin kappa variable 2/OR22-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5812]"}, {"versioned_ensembl_gene_id":"ENSG00000105221.16","gene_symbol":"AKT2","gene_name":"AKT serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:392]","synonyms":null,"biotype":"protein_coding","ncbi_id":"208","summary":"This gene is a putative oncogene encoding a protein belonging to a subfamily of serine/threonine kinases containing SH2-like (Src homology 2-like) domains, which is involved in signaling pathways. The gene serves as an oncogene in the tumorigenesis of cancer cells For example, its overexpression contributes to the malignant phenotype of a subset of human ductal pancreatic cancers. The encoded protein is a general protein kinase capable of phophorylating several known proteins, and has also been implicated in insulin signaling. [provided by RefSeq, Nov 2019]","start":40230317,"end":40285536,"strand":-1,"description":"AKT serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:392]"}, {"versioned_ensembl_gene_id":"ENSG00000163491.16","gene_symbol":"NEK10","gene_name":"NIMA related kinase 10 [Source:HGNC Symbol;Acc:HGNC:18592]","synonyms":"FLJ32685","biotype":"protein_coding","ncbi_id":"152110","summary":null,"start":27110085,"end":27369460,"strand":-1,"description":"NIMA related kinase 10 [Source:HGNC Symbol;Acc:HGNC:18592]"}, {"versioned_ensembl_gene_id":"ENSG00000183313.4","gene_symbol":"OR52L1","gene_name":"olfactory receptor family 52 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14785]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338751","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5985892,"end":5986985,"strand":-1,"description":"olfactory receptor family 52 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14785]"}, {"versioned_ensembl_gene_id":"ENSG00000182952.4","gene_symbol":"HMGN4","gene_name":"high mobility group nucleosomal binding domain 4 [Source:HGNC Symbol;Acc:HGNC:4989]","synonyms":"NHC,HMG17L3","biotype":"protein_coding","ncbi_id":"10473","summary":"The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]","start":26538405,"end":26546254,"strand":1,"description":"high mobility group nucleosomal binding domain 4 [Source:HGNC Symbol;Acc:HGNC:4989]"}, {"versioned_ensembl_gene_id":"ENSG00000187676.7","gene_symbol":"B3GLCT","gene_name":"beta 3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:20207]","synonyms":"B3GTL,B3Glc-T,B3GALTL","biotype":"protein_coding","ncbi_id":"145173","summary":"The protein encoded by this gene is a beta-1,3-glucosyltransferase that transfers glucose to O-linked fucosylglycans on thrombospondin type-1 repeats (TSRs) of several proteins. The encoded protein is a type II membrane protein. Defects in this gene are a cause of Peters-plus syndrome (PPS).[provided by RefSeq, Mar 2009]","start":31199936,"end":31332276,"strand":1,"description":"beta 3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:20207]"}, {"versioned_ensembl_gene_id":"ENSG00000229427.1","gene_symbol":"ANKRD26P4","gene_name":"ankyrin repeat domain 26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39690]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873882","summary":null,"start":31311289,"end":31312921,"strand":1,"description":"ankyrin repeat domain 26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39690]"}, {"versioned_ensembl_gene_id":"ENSG00000282461.1","gene_symbol":"AC093627.16","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151918,"end":157786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140478.15","gene_symbol":"GOLGA6D","gene_name":"golgin A6 family member D [Source:HGNC Symbol;Acc:HGNC:32204]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653643","summary":null,"start":75282835,"end":75295807,"strand":1,"description":"golgin A6 family member D [Source:HGNC Symbol;Acc:HGNC:32204]"}, {"versioned_ensembl_gene_id":"ENSG00000234855.1","gene_symbol":"SLIT1-AS1","gene_name":"SLIT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51198]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505540","summary":null,"start":97102756,"end":97103747,"strand":1,"description":"SLIT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51198]"}, {"versioned_ensembl_gene_id":"ENSG00000128739.21","gene_symbol":"SNRPN","gene_name":"small nuclear ribonucleoprotein polypeptide N [Source:HGNC Symbol;Acc:HGNC:11164]","synonyms":"SNRNP-N,SMN,SM-D,RT-LI,PWCR,HCERN3,SNURF-SNRPN","biotype":"protein_coding","ncbi_id":"6638","summary":"This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]","start":24823637,"end":24978723,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide N [Source:HGNC Symbol;Acc:HGNC:11164]"}, {"versioned_ensembl_gene_id":"ENSG00000280118.1","gene_symbol":"AC090983.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24848357,"end":24852253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270704.3","gene_symbol":"AC124312.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24984864,"end":24985173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249014.2","gene_symbol":"HMGN2P4","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33567]","synonyms":"HMGN2L4","biotype":"processed_pseudogene","ncbi_id":"643744","summary":null,"start":76242024,"end":76242404,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33567]"}, {"versioned_ensembl_gene_id":"ENSG00000220745.2","gene_symbol":"AL080276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152959359,"end":152959605,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000015133.18","gene_symbol":"CCDC88C","gene_name":"coiled-coil domain containing 88C [Source:HGNC Symbol;Acc:HGNC:19967]","synonyms":"SCA40,KIAA1509,HkRP2,DAPLE","biotype":"protein_coding","ncbi_id":"440193","summary":"This gene encodes a ubiquitously expressed coiled-coil domain-containing protein that interacts with the dishevelled protein and is a negative regulator of the Wnt signalling pathway. The protein encoded by this gene has a PDZ-domain binding motif in its C-terminus with which it interacts with the dishevelled protein. Dishevelled is a scaffold protein involved in the regulation of the Wnt signaling pathway. The Wnt signaling pathway plays an important role in embryonic development, tissue maintenance, and cancer progression. Mutations in this gene cause autosomal recessive, primary non-syndromic congenital hydrocephalus; a condition characterized by excessive accumulation of cerebrospinal fluid in the ventricles of the brain. [provided by RefSeq, Jan 2013]","start":91271323,"end":91417844,"strand":-1,"description":"coiled-coil domain containing 88C [Source:HGNC Symbol;Acc:HGNC:19967]"}, {"versioned_ensembl_gene_id":"ENSG00000226837.2","gene_symbol":"HMGB1P32","gene_name":"high mobility group box 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39123]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419995","summary":null,"start":98422138,"end":98422809,"strand":1,"description":"high mobility group box 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:39123]"}, {"versioned_ensembl_gene_id":"ENSG00000227426.1","gene_symbol":"VN1R33P","gene_name":"vomeronasal 1 receptor 33 pseudogene [Source:HGNC Symbol;Acc:HGNC:37353]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100288022","summary":null,"start":63401385,"end":63402271,"strand":-1,"description":"vomeronasal 1 receptor 33 pseudogene [Source:HGNC Symbol;Acc:HGNC:37353]"}, {"versioned_ensembl_gene_id":"ENSG00000186704.9","gene_symbol":"DTX2P1","gene_name":"DTX2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42352]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107161144","summary":null,"start":76978617,"end":77004308,"strand":1,"description":"DTX2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42352]"}, {"versioned_ensembl_gene_id":"ENSG00000255177.2","gene_symbol":"AC061979.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1242261,"end":1249676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185985.8","gene_symbol":"SLITRK2","gene_name":"SLIT and NTRK like family member 2 [Source:HGNC Symbol;Acc:HGNC:13449]","synonyms":"SLITL1,KIAA1854,CXorf2","biotype":"protein_coding","ncbi_id":"84631","summary":"This gene encodes an integral membrane protein that contains two N-terminal leucine-rich repeats domains and contains C-terminal regions similar to neurotrophin receptors. The encoded protein may play a role in modulating neurite activity. Alternatively spliced transcript variants encoding the same protein have been described.[provided by RefSeq, Feb 2010]","start":145817832,"end":145825842,"strand":1,"description":"SLIT and NTRK like family member 2 [Source:HGNC Symbol;Acc:HGNC:13449]"}, {"versioned_ensembl_gene_id":"ENSG00000242580.1","gene_symbol":"IGKV1D-43","gene_name":"immunoglobulin kappa variable 1D-43 [Source:HGNC Symbol;Acc:HGNC:5758]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28891","summary":null,"start":90209873,"end":90210529,"strand":1,"description":"immunoglobulin kappa variable 1D-43 [Source:HGNC Symbol;Acc:HGNC:5758]"}, {"versioned_ensembl_gene_id":"ENSG00000231093.1","gene_symbol":"AL391256.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145630218,"end":145632375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267436.1","gene_symbol":"AC005786.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3544199,"end":3557569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239311.1","gene_symbol":"AC092916.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111466313,"end":111497095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153283.12","gene_symbol":"CD96","gene_name":"CD96 molecule [Source:HGNC Symbol;Acc:HGNC:16892]","synonyms":"TACTILE","biotype":"protein_coding","ncbi_id":"10225","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein. The protein may play a role in the adhesive interactions of activated T and NK cells during the late phase of the immune response. It may also function in antigen presentation. Alternative splicing generates multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2016]","start":111292719,"end":111665750,"strand":1,"description":"CD96 molecule [Source:HGNC Symbol;Acc:HGNC:16892]"}, {"versioned_ensembl_gene_id":"ENSG00000240787.1","gene_symbol":"AC092916.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111570638,"end":111571054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164434.11","gene_symbol":"FABP7","gene_name":"fatty acid binding protein 7 [Source:HGNC Symbol;Acc:HGNC:3562]","synonyms":"BLBP,B-FABP","biotype":"protein_coding","ncbi_id":"2173","summary":"The gene encodes a small, highly conserved cytoplasmic protein that bind long-chain fatty acids and other hydrophobic ligands. The encoded protein is important in the establishment of the radial glial fiber in the developing brain. Alternative splicing and promoter usage results in multiple transcript variants encoding different isoforms. Pseudogenes of this gene are found on multiple chromosomes. [provided by RefSeq, Jan 2016]","start":122779475,"end":122784074,"strand":1,"description":"fatty acid binding protein 7 [Source:HGNC Symbol;Acc:HGNC:3562]"}, {"versioned_ensembl_gene_id":"ENSG00000282616.1","gene_symbol":"IGHV4-55","gene_name":"immunoglobulin heavy variable 4-55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5653]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28393","summary":null,"start":106630782,"end":106631232,"strand":-1,"description":"immunoglobulin heavy variable 4-55 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5653]"}, {"versioned_ensembl_gene_id":"ENSG00000270218.1","gene_symbol":"AC013553.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65026088,"end":65026676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284618.1","gene_symbol":"AL391294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81000150,"end":81004217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166743.9","gene_symbol":"ACSM1","gene_name":"acyl-CoA synthetase medium chain family member 1 [Source:HGNC Symbol;Acc:HGNC:18049]","synonyms":"MACS1,BUCS1","biotype":"protein_coding","ncbi_id":"116285","summary":null,"start":20623237,"end":20698890,"strand":-1,"description":"acyl-CoA synthetase medium chain family member 1 [Source:HGNC Symbol;Acc:HGNC:18049]"}, {"versioned_ensembl_gene_id":"ENSG00000251419.1","gene_symbol":"AC108120.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75831255,"end":75832764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274591.1","gene_symbol":"AC025031.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46239106,"end":46239473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233548.1","gene_symbol":"CYCSP44","gene_name":"cytochrome c, somatic pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:24418]","synonyms":"HCP44","biotype":"processed_pseudogene","ncbi_id":"349391","summary":null,"start":145176582,"end":145176894,"strand":1,"description":"cytochrome c, somatic pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:24418]"}, {"versioned_ensembl_gene_id":"ENSG00000276208.1","gene_symbol":"AL161423.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58377513,"end":58377774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251562.7","gene_symbol":"MALAT1","gene_name":"metastasis associated lung adenocarcinoma transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29665]","synonyms":"MALAT-1,LINC00047,HCN,PRO1073,NEAT2,NCRNA00047,mascRNA","biotype":"lincRNA","ncbi_id":"378938","summary":"This gene produces a precursor transcript from which a long non-coding RNA is derived by RNase P cleavage of a tRNA-like small ncRNA (known as mascRNA) from its 3' end. The resultant mature transcript lacks a canonical poly(A) tail but is instead stabilized by a 3' triple helical structure. This transcript is retained in the nucleus where it is thought to form molecular scaffolds for ribonucleoprotein complexes. It may act as a transcriptional regulator for numerous genes, including some genes involved in cancer metastasis and cell migration, and it is involved in cell cycle regulation. Its upregulation in multiple cancerous tissues has been associated with the proliferation and metastasis of tumor cells. [provided by RefSeq, Mar 2015]","start":65497762,"end":65506516,"strand":1,"description":"metastasis associated lung adenocarcinoma transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:29665]"}, {"versioned_ensembl_gene_id":"ENSG00000282188.1","gene_symbol":"IGHV3-52","gene_name":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28421","summary":null,"start":106611057,"end":106611507,"strand":-1,"description":"immunoglobulin heavy variable 3-52 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5609]"}, {"versioned_ensembl_gene_id":"ENSG00000249613.1","gene_symbol":"LINC02173","gene_name":"long intergenic non-protein coding RNA 2173 [Source:HGNC Symbol;Acc:HGNC:53035]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377355","summary":null,"start":106433624,"end":106453448,"strand":1,"description":"long intergenic non-protein coding RNA 2173 [Source:HGNC Symbol;Acc:HGNC:53035]"}, {"versioned_ensembl_gene_id":"ENSG00000229573.1","gene_symbol":"BX927250.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720050,"end":29721040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271702.1","gene_symbol":"AC123786.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77632928,"end":77633360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232739.1","gene_symbol":"AL607028.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15237492,"end":15241767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224612.1","gene_symbol":"AC079150.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153171987,"end":153201726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119048.7","gene_symbol":"UBE2B","gene_name":"ubiquitin conjugating enzyme E2 B [Source:HGNC Symbol;Acc:HGNC:12473]","synonyms":"UBC2,RAD6B,HHR6B","biotype":"protein_coding","ncbi_id":"7320","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is required for post-replicative DNA damage repair. Its protein sequence is 100% identical to the mouse, rat, and rabbit homologs, which indicates that this enzyme is highly conserved in eukaryotic evolution. [provided by RefSeq, Jul 2008]","start":134371179,"end":134391992,"strand":1,"description":"ubiquitin conjugating enzyme E2 B [Source:HGNC Symbol;Acc:HGNC:12473]"}, {"versioned_ensembl_gene_id":"ENSG00000276228.2","gene_symbol":"UBE2Q2P6","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49412]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421769","summary":null,"start":82524734,"end":82533748,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49412]"}, {"versioned_ensembl_gene_id":"ENSG00000279590.1","gene_symbol":"AC005786.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3567278,"end":3567959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227923.1","gene_symbol":"AC006455.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63354033,"end":63354365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185037.9","gene_symbol":"ZNF733P","gene_name":"zinc finger protein 733, pseudogene [Source:HGNC Symbol;Acc:HGNC:32473]","synonyms":"ZNF733","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643955","summary":null,"start":63291518,"end":63304056,"strand":-1,"description":"zinc finger protein 733, pseudogene [Source:HGNC Symbol;Acc:HGNC:32473]"}, {"versioned_ensembl_gene_id":"ENSG00000282465.1","gene_symbol":"IGHVII-49-1","gene_name":"immunoglobulin heavy variable (II)-49-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5683]","synonyms":"IGHV(II)-49-1","biotype":"IG_V_pseudogene","ncbi_id":"28364","summary":null,"start":106589056,"end":106589279,"strand":-1,"description":"immunoglobulin heavy variable (II)-49-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5683]"}, {"versioned_ensembl_gene_id":"ENSG00000278935.1","gene_symbol":"AC087386.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20141794,"end":20146430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164509.13","gene_symbol":"IL31RA","gene_name":"interleukin 31 receptor A [Source:HGNC Symbol;Acc:HGNC:18969]","synonyms":"CRL3,CRL,IL-31RA,Glmr,GLM-R","biotype":"protein_coding","ncbi_id":"133396","summary":"The protein encoded by this gene belongs to the type I cytokine receptor family. This receptor, with homology to gp130, is expressed on monocytes, and is involved in IL-31 signaling via activation of STAT-3 and STAT-5. It functions either as a monomer, or as part of a receptor complex with oncostatin M receptor (OSMR). Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jun 2011]","start":55851379,"end":55922853,"strand":1,"description":"interleukin 31 receptor A [Source:HGNC Symbol;Acc:HGNC:18969]"}, {"versioned_ensembl_gene_id":"ENSG00000198839.9","gene_symbol":"ZNF277","gene_name":"zinc finger protein 277 [Source:HGNC Symbol;Acc:HGNC:13070]","synonyms":"ZNF277P,NRIF4","biotype":"protein_coding","ncbi_id":"11179","summary":null,"start":112206588,"end":112343096,"strand":1,"description":"zinc finger protein 277 [Source:HGNC Symbol;Acc:HGNC:13070]"}, {"versioned_ensembl_gene_id":"ENSG00000259770.2","gene_symbol":"AC015871.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79944498,"end":79945578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230465.1","gene_symbol":"VENTXP4","gene_name":"VENT homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30903]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"152101","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":26346681,"end":26347638,"strand":-1,"description":"VENT homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:30903]"}, {"versioned_ensembl_gene_id":"ENSG00000148481.13","gene_symbol":"MINDY3","gene_name":"MINDY lysine 48 deubiquitinase 3 [Source:HGNC Symbol;Acc:HGNC:23578]","synonyms":"my042,FLJ13397,FAM188A,DERP5,CARP,C10orf97","biotype":"protein_coding","ncbi_id":"80013","summary":"The protein encoded by this gene contains a caspase-associated recruitment domain and may function in apoptosis. It has been identified as a tumor suppressor in lung and gastric cancers, and a polymorphism in the gene may be associated with gastric cancer risk. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":15778170,"end":15860520,"strand":-1,"description":"MINDY lysine 48 deubiquitinase 3 [Source:HGNC Symbol;Acc:HGNC:23578]"}, {"versioned_ensembl_gene_id":"ENSG00000102265.11","gene_symbol":"TIMP1","gene_name":"TIMP metallopeptidase inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:11820]","synonyms":"TIMP,EPO,CLGI","biotype":"protein_coding","ncbi_id":"7076","summary":"This gene belongs to the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases (MMPs), a group of peptidases involved in degradation of the extracellular matrix. In addition to its inhibitory role against most of the known MMPs, the encoded protein is able to promote cell proliferation in a wide range of cell types, and may also have an anti-apoptotic function. Transcription of this gene is highly inducible in response to many cytokines and hormones. In addition, the expression from some but not all inactive X chromosomes suggests that this gene inactivation is polymorphic in human females. This gene is located within intron 6 of the synapsin I gene and is transcribed in the opposite direction. [provided by RefSeq, Jul 2008]","start":47582313,"end":47586789,"strand":1,"description":"TIMP metallopeptidase inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:11820]"}, {"versioned_ensembl_gene_id":"ENSG00000232497.1","gene_symbol":"ADIPOR1P1","gene_name":"adiponectin receptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44910]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645220","summary":null,"start":22162992,"end":22165794,"strand":1,"description":"adiponectin receptor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44910]"}, {"versioned_ensembl_gene_id":"ENSG00000226139.1","gene_symbol":"BX927168.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32871715,"end":32872545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234158.1","gene_symbol":"RPEP2","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44521]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645065","summary":null,"start":26015669,"end":26016369,"strand":1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44521]"}, {"versioned_ensembl_gene_id":"ENSG00000237346.1","gene_symbol":"AL080313.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14391231,"end":14393288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261229.6","gene_symbol":"AC021483.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79843547,"end":79844304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213522.4","gene_symbol":"RAC1P5","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30593]","synonyms":"Psi1Rac1","biotype":"processed_pseudogene","ncbi_id":"402183","summary":"This locus encodes one of the pseudogenes of the functional ras-related C3 botulinum toxin substrate 1 gene (RAC1, GeneID:5879) located on chr 7. It is intronless, shares overall 93% sequence identity with the RAC1 gene, and has enough differences in the coding region so as not to be able to code for a functional protein. There is no evidence of transcription at this pseudogene locus on chr 4. [provided by RefSeq, Jul 2008]","start":107203349,"end":107203924,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30593]"}, {"versioned_ensembl_gene_id":"ENSG00000282576.1","gene_symbol":"IGHVIII-38-1","gene_name":"immunoglobulin heavy variable (III)-38-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5699]","synonyms":"IGHV(III)-38-1","biotype":"IG_V_pseudogene","ncbi_id":"28346","summary":null,"start":106442706,"end":106442759,"strand":-1,"description":"immunoglobulin heavy variable (III)-38-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5699]"}, {"versioned_ensembl_gene_id":"ENSG00000213341.10","gene_symbol":"CHUK","gene_name":"conserved helix-loop-helix ubiquitous kinase [Source:HGNC Symbol;Acc:HGNC:1974]","synonyms":"TCF16,NFKBIKA,IKKA,IKK1,IKK-alpha,IkBKA","biotype":"protein_coding","ncbi_id":"1147","summary":"This gene encodes a member of the serine/threonine protein kinase family. The encoded protein, a component of a cytokine-activated protein complex that is an inhibitor of the essential transcription factor NF-kappa-B complex, phosphorylates sites that trigger the degradation of the inhibitor via the ubiquination pathway, thereby activating the transcription factor. [provided by RefSeq, Jul 2008]","start":100188298,"end":100229619,"strand":-1,"description":"conserved helix-loop-helix ubiquitous kinase [Source:HGNC Symbol;Acc:HGNC:1974]"}, {"versioned_ensembl_gene_id":"ENSG00000278480.1","gene_symbol":"AL391094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15226373,"end":15227549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149231.11","gene_symbol":"CCDC82","gene_name":"coiled-coil domain containing 82 [Source:HGNC Symbol;Acc:HGNC:26282]","synonyms":"FLJ23518","biotype":"protein_coding","ncbi_id":"79780","summary":null,"start":96352769,"end":96389923,"strand":-1,"description":"coiled-coil domain containing 82 [Source:HGNC Symbol;Acc:HGNC:26282]"}, {"versioned_ensembl_gene_id":"ENSG00000147124.12","gene_symbol":"ZNF41","gene_name":"zinc finger protein 41 [Source:HGNC Symbol;Acc:HGNC:13107]","synonyms":"MRX89,MGC8941","biotype":"protein_coding","ncbi_id":"7592","summary":"This gene encodes a protein that contains KRAB-A and KRAB-B domains multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. An initial study suggested that this gene may be associated with X-linked cognitive disability, but a later study has called this finding into question (PMID:23871722).[provided by RefSeq, Apr 2016]","start":47445879,"end":47482946,"strand":-1,"description":"zinc finger protein 41 [Source:HGNC Symbol;Acc:HGNC:13107]"}, {"versioned_ensembl_gene_id":"ENSG00000223921.1","gene_symbol":"MTND1P27","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288227","summary":null,"start":140220584,"end":140221485,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42076]"}, {"versioned_ensembl_gene_id":"ENSG00000250298.3","gene_symbol":"GIMD1","gene_name":"GIMAP family P-loop NTPase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44141]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507096","summary":null,"start":106357485,"end":106368825,"strand":-1,"description":"GIMAP family P-loop NTPase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44141]"}, {"versioned_ensembl_gene_id":"ENSG00000198331.10","gene_symbol":"HYLS1","gene_name":"HYLS1, centriolar and ciliogenesis associated [Source:HGNC Symbol;Acc:HGNC:26558]","synonyms":"FLJ32915","biotype":"protein_coding","ncbi_id":"219844","summary":"This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2008]","start":125883614,"end":125900648,"strand":1,"description":"HYLS1, centriolar and ciliogenesis associated [Source:HGNC Symbol;Acc:HGNC:26558]"}, {"versioned_ensembl_gene_id":"ENSG00000274345.1","gene_symbol":"AC010492.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54229658,"end":54230835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170935.7","gene_symbol":"NCBP2L","gene_name":"nuclear cap binding protein subunit 2 like [Source:HGNC Symbol;Acc:HGNC:31795]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392517","summary":null,"start":107774899,"end":107795829,"strand":1,"description":"nuclear cap binding protein subunit 2 like [Source:HGNC Symbol;Acc:HGNC:31795]"}, {"versioned_ensembl_gene_id":"ENSG00000163623.9","gene_symbol":"NKX6-1","gene_name":"NK6 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7839]","synonyms":"NKX6A,Nkx6.1","biotype":"protein_coding","ncbi_id":"4825","summary":"In the pancreas, NKX6.1 is required for the development of beta cells and is a potent bifunctional transcription regulator that binds to AT-rich sequences within the promoter region of target genes Iype et al. (2004) [PubMed 15056733].[supplied by OMIM, Mar 2008]","start":84491987,"end":84498450,"strand":-1,"description":"NK6 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7839]"}, {"versioned_ensembl_gene_id":"ENSG00000237192.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30141872,"end":30150859,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000145861.7","gene_symbol":"C1QTNF2","gene_name":"C1q and TNF related 2 [Source:HGNC Symbol;Acc:HGNC:14325]","synonyms":"CTRP2","biotype":"protein_coding","ncbi_id":"114898","summary":null,"start":160347751,"end":160370641,"strand":-1,"description":"C1q and TNF related 2 [Source:HGNC Symbol;Acc:HGNC:14325]"}, {"versioned_ensembl_gene_id":"ENSG00000164078.12","gene_symbol":"MST1R","gene_name":"macrophage stimulating 1 receptor [Source:HGNC Symbol;Acc:HGNC:7381]","synonyms":"RON,PTK8,CDw136,CD136","biotype":"protein_coding","ncbi_id":"4486","summary":"This gene encodes a cell surface receptor for macrophage-stimulating protein (MSP) with tyrosine kinase activity. The mature form of this protein is a heterodimer of disulfide-linked alpha and beta subunits, generated by proteolytic cleavage of a single-chain precursor. The beta subunit undergoes tyrosine phosphorylation upon stimulation by MSP. This protein is expressed on the ciliated epithelia of the mucociliary transport apparatus of the lung, and together with MSP, thought to be involved in host defense. Alternative splicing generates multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Jan 2016]","start":49887002,"end":49903873,"strand":-1,"description":"macrophage stimulating 1 receptor [Source:HGNC Symbol;Acc:HGNC:7381]"}, {"versioned_ensembl_gene_id":"ENSG00000107829.13","gene_symbol":"FBXW4","gene_name":"F-box and WD repeat domain containing 4 [Source:HGNC Symbol;Acc:HGNC:10847]","synonyms":"SHFM3,Fbw4,dactylin","biotype":"protein_coding","ncbi_id":"6468","summary":"This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22. [provided by RefSeq, Jul 2008]","start":101610664,"end":101695295,"strand":-1,"description":"F-box and WD repeat domain containing 4 [Source:HGNC Symbol;Acc:HGNC:10847]"}, {"versioned_ensembl_gene_id":"ENSG00000170340.10","gene_symbol":"B3GNT2","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15629]","synonyms":"BETA3GNT,B3GNT1,B3GNT-2,B3GN-T2,B3GN-T1","biotype":"protein_coding","ncbi_id":"10678","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II transmembrane protein. It prefers the substrate of lacto-N-neotetraose, and is involved in the biosynthesis of poly-N-acetyllactosamine chains. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2016]","start":62196113,"end":62224731,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:15629]"}, {"versioned_ensembl_gene_id":"ENSG00000126226.21","gene_symbol":"PCID2","gene_name":"PCI domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25653]","synonyms":"FLJ11305","biotype":"protein_coding","ncbi_id":"55795","summary":"This gene encodes a component of the TREX-2 complex (transcription and export complex 2), which regulates mRNA export from the nucleus. This protein regulates expression of Mad2 mitotic arrest deficient-like 1, a cell division checkpoint protein. This protein also interacts with and stabilizes Brca2 (breast cancer 2) protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":113177539,"end":113208715,"strand":-1,"description":"PCI domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25653]"}, {"versioned_ensembl_gene_id":"ENSG00000258650.1","gene_symbol":"HSBP1P1","gene_name":"heat shock factor binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20053]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326296","summary":null,"start":58463971,"end":58464136,"strand":1,"description":"heat shock factor binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20053]"}, {"versioned_ensembl_gene_id":"ENSG00000235833.1","gene_symbol":"AC017099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97523949,"end":97524976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228714.2","gene_symbol":"AL731897.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115739663,"end":115744239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204148.3","gene_symbol":"LINC00474","gene_name":"long intergenic non-protein coding RNA 474 [Source:HGNC Symbol;Acc:HGNC:23367]","synonyms":"EST-YD1,C9orf27","biotype":"lincRNA","ncbi_id":"58483","summary":null,"start":115888169,"end":115925207,"strand":-1,"description":"long intergenic non-protein coding RNA 474 [Source:HGNC Symbol;Acc:HGNC:23367]"}, {"versioned_ensembl_gene_id":"ENSG00000144771.7","gene_symbol":"LRTM1","gene_name":"leucine rich repeats and transmembrane domains 1 [Source:HGNC Symbol;Acc:HGNC:25023]","synonyms":"HT017","biotype":"protein_coding","ncbi_id":"57408","summary":null,"start":54918237,"end":54967088,"strand":-1,"description":"leucine rich repeats and transmembrane domains 1 [Source:HGNC Symbol;Acc:HGNC:25023]"}, {"versioned_ensembl_gene_id":"ENSG00000240698.1","gene_symbol":"AP002453.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108690289,"end":108690956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139636.15","gene_symbol":"LMBR1L","gene_name":"limb development membrane protein 1 like [Source:HGNC Symbol;Acc:HGNC:18268]","synonyms":"KIAA1174,FLJ10494","biotype":"protein_coding","ncbi_id":"55716","summary":null,"start":49096551,"end":49110900,"strand":-1,"description":"limb development membrane protein 1 like [Source:HGNC Symbol;Acc:HGNC:18268]"}, {"versioned_ensembl_gene_id":"ENSG00000243230.1","gene_symbol":"AC011005.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129209775,"end":129213545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251611.1","gene_symbol":"AC079795.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151407551,"end":151408835,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270265.1","gene_symbol":"AC104819.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151333775,"end":151353224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123268.8","gene_symbol":"ATF1","gene_name":"activating transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:783]","synonyms":"TREB36","biotype":"protein_coding","ncbi_id":"466","summary":"This gene encodes an activating transcription factor, which belongs to the ATF subfamily and bZIP (basic-region leucine zipper) family. It influences cellular physiologic processes by regulating the expression of downstream target genes, which are related to growth, survival, and other cellular activities. This protein is phosphorylated at serine 63 in its kinase-inducible domain by serine/threonine kinases, cAMP-dependent protein kinase A, calmodulin-dependent protein kinase I/II, mitogen- and stress-activated protein kinase and cyclin-dependent kinase 3 (cdk-3). Its phosphorylation enhances its transactivation and transcriptional activities, and enhances cell transformation. Fusion of this gene and FUS on chromosome 16 or EWSR1 on chromosome 22 induced by translocation generates chimeric proteins in angiomatoid fibrous histiocytoma and clear cell sarcoma. This gene has a pseudogene on chromosome 6. [provided by RefSeq, Aug 2010]","start":50763710,"end":50821122,"strand":1,"description":"activating transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:783]"}, {"versioned_ensembl_gene_id":"ENSG00000244537.2","gene_symbol":"KRTAP4-2","gene_name":"keratin associated protein 4-2 [Source:HGNC Symbol;Acc:HGNC:18900]","synonyms":"KAP4.2","biotype":"protein_coding","ncbi_id":"85291","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41177446,"end":41178208,"strand":-1,"description":"keratin associated protein 4-2 [Source:HGNC Symbol;Acc:HGNC:18900]"}, {"versioned_ensembl_gene_id":"ENSG00000251439.1","gene_symbol":"AC006070.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41186944,"end":41187136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151952.15","gene_symbol":"TMEM132D","gene_name":"transmembrane protein 132D [Source:HGNC Symbol;Acc:HGNC:29411]","synonyms":"PPP1R153,MOLT,KIAA1944","biotype":"protein_coding","ncbi_id":"121256","summary":null,"start":129071725,"end":129903666,"strand":-1,"description":"transmembrane protein 132D [Source:HGNC Symbol;Acc:HGNC:29411]"}, {"versioned_ensembl_gene_id":"ENSG00000256137.1","gene_symbol":"AC117373.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129681427,"end":129698227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171396.11","gene_symbol":"KRTAP4-4","gene_name":"keratin associated protein 4-4 [Source:HGNC Symbol;Acc:HGNC:16928]","synonyms":"KRTAP4-13,KAP4.4,KAP4.13","biotype":"protein_coding","ncbi_id":"84616","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41159651,"end":41160731,"strand":-1,"description":"keratin associated protein 4-4 [Source:HGNC Symbol;Acc:HGNC:16928]"}, {"versioned_ensembl_gene_id":"ENSG00000280196.1","gene_symbol":"AC055717.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":129839928,"end":129840522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166002.6","gene_symbol":"SMCO4","gene_name":"single-pass membrane protein with coiled-coil domains 4 [Source:HGNC Symbol;Acc:HGNC:24810]","synonyms":"FN5,C11orf75","biotype":"protein_coding","ncbi_id":"56935","summary":null,"start":93478472,"end":93543508,"strand":-1,"description":"single-pass membrane protein with coiled-coil domains 4 [Source:HGNC Symbol;Acc:HGNC:24810]"}, {"versioned_ensembl_gene_id":"ENSG00000220076.1","gene_symbol":"AL034345.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38928031,"end":38928153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170099.5","gene_symbol":"SERPINA6","gene_name":"serpin family A member 6 [Source:HGNC Symbol;Acc:HGNC:1540]","synonyms":"CBG","biotype":"protein_coding","ncbi_id":"866","summary":"This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008]","start":94304248,"end":94323394,"strand":-1,"description":"serpin family A member 6 [Source:HGNC Symbol;Acc:HGNC:1540]"}, {"versioned_ensembl_gene_id":"ENSG00000116221.15","gene_symbol":"MRPL37","gene_name":"mitochondrial ribosomal protein L37 [Source:HGNC Symbol;Acc:HGNC:14034]","synonyms":"RPML2,MRP-L2","biotype":"protein_coding","ncbi_id":"51253","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":54184041,"end":54225464,"strand":1,"description":"mitochondrial ribosomal protein L37 [Source:HGNC Symbol;Acc:HGNC:14034]"}, {"versioned_ensembl_gene_id":"ENSG00000170231.15","gene_symbol":"FABP6","gene_name":"fatty acid binding protein 6 [Source:HGNC Symbol;Acc:HGNC:3561]","synonyms":"ILLBP,ILBP3,ILBP,I-BAP,I-BALB,I-BABP,I-15P","biotype":"protein_coding","ncbi_id":"2172","summary":"This gene encodes the ileal fatty acid binding protein. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABP6 and FABP1 (the liver fatty acid binding protein) are also able to bind bile acids. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism. Transcript variants generated by alternate transcription promoters and/or alternate splicing have been found for this gene. [provided by RefSeq, Jul 2008]","start":160187367,"end":160238735,"strand":1,"description":"fatty acid binding protein 6 [Source:HGNC Symbol;Acc:HGNC:3561]"}, {"versioned_ensembl_gene_id":"ENSG00000250145.1","gene_symbol":"AC114940.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106543066,"end":106544330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261695.1","gene_symbol":"AC136443.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14734685,"end":14746177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254609.1","gene_symbol":"AC136443.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14727282,"end":14733347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162419.12","gene_symbol":"GMEB1","gene_name":"glucocorticoid modulatory element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4370]","synonyms":"PIF96,P96PIF","biotype":"protein_coding","ncbi_id":"10691","summary":"This gene encodes a member of KDWK gene family which associates with GMEB2 protein. The GMEB1-GMEB2 complex is essential for parvovirus DNA replication. Studies in rat for a similar gene suggest that this gene's role is to modulate the transactivation of the glucocorticoid receptor when it is bound to glucocorticoid response elements. Three alternative spliced transcript variants encoding different isoforms exist. [provided by RefSeq, Feb 2016]","start":28668732,"end":28719353,"strand":1,"description":"glucocorticoid modulatory element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4370]"}, {"versioned_ensembl_gene_id":"ENSG00000229030.1","gene_symbol":"BX276092.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71848775,"end":71849004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232081.1","gene_symbol":"LARGE-IT1","gene_name":"LARGE intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41357]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874331","summary":null,"start":33723832,"end":33724912,"strand":-1,"description":"LARGE intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41357]"}, {"versioned_ensembl_gene_id":"ENSG00000196248.5","gene_symbol":"OR10S1","gene_name":"olfactory receptor family 10 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14807]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219873","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123976661,"end":123977781,"strand":-1,"description":"olfactory receptor family 10 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:14807]"}, {"versioned_ensembl_gene_id":"ENSG00000181499.2","gene_symbol":"OR6T1","gene_name":"olfactory receptor family 6 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14848]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219874","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":123942785,"end":123943873,"strand":-1,"description":"olfactory receptor family 6 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14848]"}, {"versioned_ensembl_gene_id":"ENSG00000264290.1","gene_symbol":"AC104564.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29569580,"end":29570519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214548.14","gene_symbol":"MEG3","gene_name":"maternally expressed 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14575]","synonyms":"onco-lncRNA-83,NCRNA00023,LINC00023,GTL2","biotype":"lincRNA","ncbi_id":"55384","summary":"This gene is a maternally expressed imprinted gene. Multiple alternatively spliced transcript variants have been transcribed from this gene and all of them are long non-coding RNAs (lncRNAs). This gene is expressed in many normal tissues, but its expression is lost in multiple cancer cell lines of various tissue origins. It inhibits tumor cell proliferation in vitro. It also interacts with the tumor suppressor p53, and regulates p53 target gene expression. Its deletion enhances angiogenesis in vivo. Many experimental evidences demonstrate that this gene is a lncRNA tumor suppressor. [provided by RefSeq, Mar 2012]","start":100779410,"end":100861031,"strand":1,"description":"maternally expressed 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:14575]"}, {"versioned_ensembl_gene_id":"ENSG00000253311.2","gene_symbol":"LINC01847","gene_name":"long intergenic non-protein coding RNA 1847 [Source:HGNC Symbol;Acc:HGNC:52662]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927766","summary":null,"start":159698586,"end":159937766,"strand":-1,"description":"long intergenic non-protein coding RNA 1847 [Source:HGNC Symbol;Acc:HGNC:52662]"}, {"versioned_ensembl_gene_id":"ENSG00000232988.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29890694,"end":29891825,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000159409.14","gene_symbol":"CELF3","gene_name":"CUGBP Elav-like family member 3 [Source:HGNC Symbol;Acc:HGNC:11967]","synonyms":"TNRC4,MGC57297,ERDA4,CAGH4,BRUNOL1","biotype":"protein_coding","ncbi_id":"11189","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]","start":151702404,"end":151716814,"strand":-1,"description":"CUGBP Elav-like family member 3 [Source:HGNC Symbol;Acc:HGNC:11967]"}, {"versioned_ensembl_gene_id":"ENSG00000230532.1","gene_symbol":"AC091133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48931791,"end":48937100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271614.1","gene_symbol":"ATP2B1-AS1","gene_name":"ATP2B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27883]","synonyms":"LINC00936","biotype":"lincRNA","ncbi_id":"338758","summary":null,"start":89708959,"end":89712590,"strand":1,"description":"ATP2B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27883]"}, {"versioned_ensembl_gene_id":"ENSG00000270103.3","gene_symbol":"AL360012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28648600,"end":28648730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169679.14","gene_symbol":"BUB1","gene_name":"BUB1 mitotic checkpoint serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1148]","synonyms":"hBUB1,BUB1L,BUB1A","biotype":"protein_coding","ncbi_id":"699","summary":"This gene encodes a serine/threonine-protein kinase that play a central role in mitosis. The encoded protein functions in part by phosphorylating members of the mitotic checkpoint complex and activating the spindle checkpoint. This protein also plays a role in inhibiting the activation of the anaphase promoting complex/cyclosome. This protein may also function in the DNA damage response. Mutations in this gene have been associated with aneuploidy and several forms of cancer. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":110637698,"end":110678114,"strand":-1,"description":"BUB1 mitotic checkpoint serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1148]"}, {"versioned_ensembl_gene_id":"ENSG00000264448.5","gene_symbol":"AC084346.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93915734,"end":93916682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240074.1","gene_symbol":"AC104982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29855759,"end":29856332,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215113.6","gene_symbol":"CXorf49B","gene_name":"chromosome X open reading frame 49B [Source:HGNC Symbol;Acc:HGNC:34229]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132994","summary":null,"start":71763424,"end":71767204,"strand":1,"description":"chromosome X open reading frame 49B [Source:HGNC Symbol;Acc:HGNC:34229]"}, {"versioned_ensembl_gene_id":"ENSG00000172809.12","gene_symbol":"RPL38","gene_name":"ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:10349]","synonyms":"L38","biotype":"protein_coding","ncbi_id":"6169","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L38E family of ribosomal proteins. It is located in the cytoplasm. Alternative splice variants have been identified, both encoding the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome, including one located in the promoter region of the type 1 angiotensin II receptor gene. [provided by RefSeq, Jul 2008]","start":74203582,"end":74210655,"strand":1,"description":"ribosomal protein L38 [Source:HGNC Symbol;Acc:HGNC:10349]"}, {"versioned_ensembl_gene_id":"ENSG00000174917.8","gene_symbol":"C19orf70","gene_name":"chromosome 19 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33702]","synonyms":"QIL1,P117,MIC13","biotype":"protein_coding","ncbi_id":"125988","summary":null,"start":5678421,"end":5680896,"strand":-1,"description":"chromosome 19 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:33702]"}, {"versioned_ensembl_gene_id":"ENSG00000234721.2","gene_symbol":"LINC02092","gene_name":"long intergenic non-protein coding RNA 2092 [Source:HGNC Symbol;Acc:HGNC:52943]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400620","summary":null,"start":73786802,"end":73800793,"strand":1,"description":"long intergenic non-protein coding RNA 2092 [Source:HGNC Symbol;Acc:HGNC:52943]"}, {"versioned_ensembl_gene_id":"ENSG00000263574.1","gene_symbol":"AC125421.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73737854,"end":73756557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124444.15","gene_symbol":"ZNF576","gene_name":"zinc finger protein 576 [Source:HGNC Symbol;Acc:HGNC:28357]","synonyms":"MGC2508","biotype":"protein_coding","ncbi_id":"79177","summary":null,"start":43596392,"end":43601157,"strand":1,"description":"zinc finger protein 576 [Source:HGNC Symbol;Acc:HGNC:28357]"}, {"versioned_ensembl_gene_id":"ENSG00000189362.11","gene_symbol":"NEMP2","gene_name":"nuclear envelope integral membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:33700]","synonyms":"TMEM194B","biotype":"protein_coding","ncbi_id":"100131211","summary":null,"start":190504342,"end":190534722,"strand":-1,"description":"nuclear envelope integral membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:33700]"}, {"versioned_ensembl_gene_id":"ENSG00000159210.9","gene_symbol":"SNF8","gene_name":"SNF8, ESCRT-II complex subunit [Source:HGNC Symbol;Acc:HGNC:17028]","synonyms":"VPS22,EAP30,Dot3","biotype":"protein_coding","ncbi_id":"11267","summary":"The protein encoded by this gene is a component of the endosomal sorting complex required for transport II (ESCRT-II), which regulates the movement of ubiquitinylated transmembrane proteins to the lysosome for degradation. This complex also interacts with the RNA polymerase II elongation factor (ELL) to overcome the repressive effects of ELL on RNA polymerase II activity. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":48929316,"end":48945117,"strand":-1,"description":"SNF8, ESCRT-II complex subunit [Source:HGNC Symbol;Acc:HGNC:17028]"}, {"versioned_ensembl_gene_id":"ENSG00000226402.8","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30092809,"end":30103024,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000265935.1","gene_symbol":"AC032019.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73662568,"end":73663848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238027.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30095152,"end":30104642,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000109684.14","gene_symbol":"CLNK","gene_name":"cytokine dependent hematopoietic cell linker [Source:HGNC Symbol;Acc:HGNC:17438]","synonyms":"MIST","biotype":"protein_coding","ncbi_id":"116449","summary":"MIST is a member of the SLP76 family of adaptors (see LCP2, MIM 601603; BLNK, MIM 604515). MIST plays a role in the regulation of immunoreceptor signaling, including PLC-gamma (PLCG1; MIM 172420)-mediated B cell antigen receptor (BCR) signaling and FC-epsilon R1 (see FCER1A, MIM 147140)-mediated mast cell degranulation (Cao et al., 1999 [PubMed 10562326]; Goitsuka et al., 2000, 2001 [PubMed 10744659] [PubMed 11463797]).[supplied by OMIM, Mar 2008]","start":10486395,"end":10684865,"strand":-1,"description":"cytokine dependent hematopoietic cell linker [Source:HGNC Symbol;Acc:HGNC:17438]"}, {"versioned_ensembl_gene_id":"ENSG00000141499.16","gene_symbol":"WRAP53","gene_name":"WD repeat containing antisense to TP53 [Source:HGNC Symbol;Acc:HGNC:25522]","synonyms":"FLJ10385,WDR79,TCAB1","biotype":"protein_coding","ncbi_id":"55135","summary":"This gene encodes an essential component of the telomerase holoenzyme complex, a ribonucleoprotein complex required for telomere synthesis. This protein is enriched in Cajal bodies, nuclear sites of RNP processing that are important for telomerase function. It interacts with dyskerin, TERT and TERC, other components of active telomerase, and with small Cajal body RNAs (scaRNAs), which are involved in modifying splicing RNAs. This mRNA also functions as a p53 antisense transcript, that regulates endogenous p53 mRNA levels and further induction of p53 protein by targeting the 5' untranslated region of p53 mRNA. Alternatively spliced transcript variants which differ only in the 5' UTR have been found for this gene. [provided by RefSeq, Mar 2011]","start":7686071,"end":7703502,"strand":1,"description":"WD repeat containing antisense to TP53 [Source:HGNC Symbol;Acc:HGNC:25522]"}, {"versioned_ensembl_gene_id":"ENSG00000204344.14","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31971091,"end":31982821,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000104805.15","gene_symbol":"NUCB1","gene_name":"nucleobindin 1 [Source:HGNC Symbol;Acc:HGNC:8043]","synonyms":"NUC,Calnuc","biotype":"protein_coding","ncbi_id":"4924","summary":"This gene encodes a member of a small calcium-binding EF-hand protein family. The encoded protein is thought to have a key role in Golgi calcium homeostasis and Ca(2+)-regulated signal transduction events. [provided by RefSeq, Jun 2010]","start":48900050,"end":48923372,"strand":1,"description":"nucleobindin 1 [Source:HGNC Symbol;Acc:HGNC:8043]"}, {"versioned_ensembl_gene_id":"ENSG00000280587.1","gene_symbol":"FP700125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":235065479,"end":235074220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231070.1","gene_symbol":"OR52Y1P","gene_name":"olfactory receptor family 52 subfamily Y member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15240]","synonyms":"OR52Y2P","biotype":"unprocessed_pseudogene","ncbi_id":"81240","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4793778,"end":4795284,"strand":-1,"description":"olfactory receptor family 52 subfamily Y member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15240]"}, {"versioned_ensembl_gene_id":"ENSG00000276051.4","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29826986,"end":29831158,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000253657.1","gene_symbol":"AC022634.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108572643,"end":108573174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176904.2","gene_symbol":"OR51H1","gene_name":"olfactory receptor family 51 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14833]","synonyms":"OR51H1P","biotype":"protein_coding","ncbi_id":"401663","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4859656,"end":4863652,"strand":-1,"description":"olfactory receptor family 51 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14833]"}, {"versioned_ensembl_gene_id":"ENSG00000255291.2","gene_symbol":"HMGB1P40","gene_name":"high mobility group box 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39187]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506595","summary":null,"start":20574186,"end":20575042,"strand":1,"description":"high mobility group box 1 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39187]"}, {"versioned_ensembl_gene_id":"ENSG00000235714.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29812592,"end":29812723,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000257341.5","gene_symbol":"AL928654.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":105487199,"end":105492267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237554.4","gene_symbol":"CR925767.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29803224,"end":29804020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163322.13","gene_symbol":"ABRAXAS1","gene_name":"abraxas 1, BRCA1 A complex subunit [Source:HGNC Symbol;Acc:HGNC:25829]","synonyms":"FLJ13614,FAM175A,CCDC98,ABRAXAS,ABRA1","biotype":"protein_coding","ncbi_id":"84142","summary":"This gene encodes a protein that binds to the C-terminal repeats of breast cancer 1 (BRCA1) through a phospho-SXXF motif. The encoded protein recruits ubiquitin interaction motif containing 1 protein to BRCA1 protein and is required for DNA damage resistance, DNA repair, and cell cycle checkpoint control. Pseudogenes of this gene are found on chromosomes 3 and 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":83459517,"end":83523348,"strand":-1,"description":"abraxas 1, BRCA1 A complex subunit [Source:HGNC Symbol;Acc:HGNC:25829]"}, {"versioned_ensembl_gene_id":"ENSG00000184432.9","gene_symbol":"COPB2","gene_name":"coatomer protein complex subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:2232]","synonyms":"betaprime-COP,beta'-COP","biotype":"protein_coding","ncbi_id":"9276","summary":"The Golgi coatomer complex (see MIM 601924) constitutes the coat of nonclathrin-coated vesicles and is essential for Golgi budding and vesicular trafficking. It consists of 7 protein subunits, including COPB2.[supplied by OMIM, Jul 2002]","start":139355600,"end":139389732,"strand":-1,"description":"coatomer protein complex subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:2232]"}, {"versioned_ensembl_gene_id":"ENSG00000206260.3","gene_symbol":"PRR23A","gene_name":"proline rich 23A [Source:HGNC Symbol;Acc:HGNC:37172]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729627","summary":null,"start":139005468,"end":139006268,"strand":-1,"description":"proline rich 23A [Source:HGNC Symbol;Acc:HGNC:37172]"}, {"versioned_ensembl_gene_id":"ENSG00000229604.2","gene_symbol":"MTATP8P2","gene_name":"mitochondrially encoded ATP synthase 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44572]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479042","summary":null,"start":87824942,"end":87825143,"strand":1,"description":"mitochondrially encoded ATP synthase 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44572]"}, {"versioned_ensembl_gene_id":"ENSG00000224973.5","gene_symbol":"LARGE-AS1","gene_name":"LARGE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40336]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100506195","summary":null,"start":33725014,"end":33750843,"strand":1,"description":"LARGE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40336]"}, {"versioned_ensembl_gene_id":"ENSG00000141510.16","gene_symbol":"TP53","gene_name":"tumor protein p53 [Source:HGNC Symbol;Acc:HGNC:11998]","synonyms":"p53,LFS1","biotype":"protein_coding","ncbi_id":"7157","summary":"This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016]","start":7661779,"end":7687550,"strand":-1,"description":"tumor protein p53 [Source:HGNC Symbol;Acc:HGNC:11998]"}, {"versioned_ensembl_gene_id":"ENSG00000165521.15","gene_symbol":"EML5","gene_name":"echinoderm microtubule associated protein like 5 [Source:HGNC Symbol;Acc:HGNC:18197]","synonyms":"HuEMAP-2,EMAP-2","biotype":"protein_coding","ncbi_id":"161436","summary":null,"start":88612431,"end":88792752,"strand":-1,"description":"echinoderm microtubule associated protein like 5 [Source:HGNC Symbol;Acc:HGNC:18197]"}, {"versioned_ensembl_gene_id":"ENSG00000250847.1","gene_symbol":"AC010350.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":121195980,"end":121196210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166411.13","gene_symbol":"IDH3A","gene_name":"isocitrate dehydrogenase 3 (NAD(+)) alpha [Source:HGNC Symbol;Acc:HGNC:5384]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3419","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. NAD(+)-dependent isocitrate dehydrogenases catalyze the allosterically regulated rate-limiting step of the tricarboxylic acid cycle. Each isozyme is a heterotetramer that is composed of two alpha subunits, one beta subunit, and one gamma subunit. The protein encoded by this gene is the alpha subunit of one isozyme of NAD(+)-dependent isocitrate dehydrogenase. [provided by RefSeq, Jul 2008]","start":78131498,"end":78171949,"strand":1,"description":"isocitrate dehydrogenase 3 (NAD(+)) alpha [Source:HGNC Symbol;Acc:HGNC:5384]"}, {"versioned_ensembl_gene_id":"ENSG00000248545.2","gene_symbol":"AC092436.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25608711,"end":25619468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183476.12","gene_symbol":"SH2D7","gene_name":"SH2 domain containing 7 [Source:HGNC Symbol;Acc:HGNC:34549]","synonyms":"LOC646892","biotype":"protein_coding","ncbi_id":"646892","summary":null,"start":78077808,"end":78104909,"strand":1,"description":"SH2 domain containing 7 [Source:HGNC Symbol;Acc:HGNC:34549]"}, {"versioned_ensembl_gene_id":"ENSG00000239732.3","gene_symbol":"TLR9","gene_name":"toll like receptor 9 [Source:HGNC Symbol;Acc:HGNC:15633]","synonyms":"CD289","biotype":"protein_coding","ncbi_id":"54106","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family, which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. Studies in mice and human indicate that this receptor mediates cellular response to unmethylated CpG dinucleotides in bacterial DNA to mount an innate immune response. [provided by RefSeq, Aug 2017]","start":52221080,"end":52226163,"strand":-1,"description":"toll like receptor 9 [Source:HGNC Symbol;Acc:HGNC:15633]"}, {"versioned_ensembl_gene_id":"ENSG00000249320.1","gene_symbol":"AC133963.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25472517,"end":25473815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197608.11","gene_symbol":"ZNF841","gene_name":"zinc finger protein 841 [Source:HGNC Symbol;Acc:HGNC:27611]","synonyms":"LOC284371","biotype":"protein_coding","ncbi_id":"284371","summary":null,"start":52064466,"end":52095765,"strand":-1,"description":"zinc finger protein 841 [Source:HGNC Symbol;Acc:HGNC:27611]"}, {"versioned_ensembl_gene_id":"ENSG00000248927.1","gene_symbol":"AC114284.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120781218,"end":120790778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280379.1","gene_symbol":"AP003072.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93171134,"end":93171906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173917.10","gene_symbol":"HOXB2","gene_name":"homeobox B2 [Source:HGNC Symbol;Acc:HGNC:5113]","synonyms":"HOX2H,HOX2","biotype":"protein_coding","ncbi_id":"3212","summary":"This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer. [provided by RefSeq, Jul 2008]","start":48540894,"end":48544989,"strand":-1,"description":"homeobox B2 [Source:HGNC Symbol;Acc:HGNC:5113]"}, {"versioned_ensembl_gene_id":"ENSG00000232238.1","gene_symbol":"RPS29P8","gene_name":"ribosomal protein S29 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132376","summary":null,"start":148595158,"end":148595328,"strand":1,"description":"ribosomal protein S29 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36915]"}, {"versioned_ensembl_gene_id":"ENSG00000284413.2","gene_symbol":"BTBD8","gene_name":"BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:21019]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284697","summary":null,"start":92080305,"end":92150882,"strand":1,"description":"BTB domain containing 8 [Source:HGNC Symbol;Acc:HGNC:21019]"}, {"versioned_ensembl_gene_id":"ENSG00000233401.1","gene_symbol":"PRKAR1AP1","gene_name":"protein kinase cAMP-dependent type I regulatory subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9389]","synonyms":"PRKAR1AP","biotype":"processed_pseudogene","ncbi_id":"5574","summary":null,"start":92125301,"end":92126462,"strand":1,"description":"protein kinase cAMP-dependent type I regulatory subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9389]"}, {"versioned_ensembl_gene_id":"ENSG00000183054.11","gene_symbol":"RGPD6","gene_name":"RANBP2-like and GRIP domain containing 6 [Source:HGNC Symbol;Acc:HGNC:32419]","synonyms":"RGP6","biotype":"protein_coding","ncbi_id":"729540","summary":null,"start":110513812,"end":110577185,"strand":-1,"description":"RANBP2-like and GRIP domain containing 6 [Source:HGNC Symbol;Acc:HGNC:32419]"}, {"versioned_ensembl_gene_id":"ENSG00000267577.1","gene_symbol":"AC010327.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55158939,"end":55177540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172878.13","gene_symbol":"METAP1D","gene_name":"methionyl aminopeptidase type 1D, mitochondrial [Source:HGNC Symbol;Acc:HGNC:32583]","synonyms":"Metap1l,MAP1D","biotype":"protein_coding","ncbi_id":"254042","summary":"The N-terminal methionine excision pathway is an essential process in which the N-terminal methionine is removed from many proteins, thus facilitating subsequent protein modification. In mitochondria, enzymes that catalyze this reaction are celled methionine aminopeptidases (MetAps, or MAPs; EC 3.4.11.18) (Serero et al., 2003 [PubMed 14532271]).[supplied by OMIM, Mar 2008]","start":171999583,"end":172082430,"strand":1,"description":"methionyl aminopeptidase type 1D, mitochondrial [Source:HGNC Symbol;Acc:HGNC:32583]"}, {"versioned_ensembl_gene_id":"ENSG00000243687.1","gene_symbol":"AC079594.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160342685,"end":160343015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213186.7","gene_symbol":"TRIM59","gene_name":"tripartite motif containing 59 [Source:HGNC Symbol;Acc:HGNC:30834]","synonyms":"TSBF1,TRIM57,RNF104,Mrf1","biotype":"protein_coding","ncbi_id":"286827","summary":null,"start":160432445,"end":160485773,"strand":-1,"description":"tripartite motif containing 59 [Source:HGNC Symbol;Acc:HGNC:30834]"}, {"versioned_ensembl_gene_id":"ENSG00000103253.17","gene_symbol":"HAGHL","gene_name":"hydroxyacylglutathione hydrolase like [Source:HGNC Symbol;Acc:HGNC:14177]","synonyms":"MGC2605","biotype":"protein_coding","ncbi_id":"84264","summary":null,"start":726936,"end":735525,"strand":1,"description":"hydroxyacylglutathione hydrolase like [Source:HGNC Symbol;Acc:HGNC:14177]"}, {"versioned_ensembl_gene_id":"ENSG00000248777.1","gene_symbol":"AC006499.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10199823,"end":10200672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278484.1","gene_symbol":"AC010998.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120984966,"end":120985596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000035928.15","gene_symbol":"RFC1","gene_name":"replication factor C subunit 1 [Source:HGNC Symbol;Acc:HGNC:9969]","synonyms":"RFC140,PO-GA,MHCBFB,A1","biotype":"protein_coding","ncbi_id":"5981","summary":"This gene encodes the large subunit of replication factor C, a five subunit DNA polymerase accessory protein, which is a DNA-dependent ATPase required for eukaryotic DNA replication and repair. The large subunit acts as an activator of DNA polymerases, binds to the 3' end of primers, and promotes coordinated synthesis of both strands. It may also have a role in telomere stability. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2011]","start":39287456,"end":39366375,"strand":-1,"description":"replication factor C subunit 1 [Source:HGNC Symbol;Acc:HGNC:9969]"}, {"versioned_ensembl_gene_id":"ENSG00000206507.9","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29791100,"end":29797819,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000264522.5","gene_symbol":"OTUD7B","gene_name":"OTU deubiquitinase 7B [Source:HGNC Symbol;Acc:HGNC:16683]","synonyms":"ZA20D1,CEZANNE","biotype":"protein_coding","ncbi_id":"56957","summary":null,"start":149937812,"end":150010676,"strand":-1,"description":"OTU deubiquitinase 7B [Source:HGNC Symbol;Acc:HGNC:16683]"}, {"versioned_ensembl_gene_id":"ENSG00000115840.13","gene_symbol":"SLC25A12","gene_name":"solute carrier family 25 member 12 [Source:HGNC Symbol;Acc:HGNC:10982]","synonyms":"Aralar","biotype":"protein_coding","ncbi_id":"8604","summary":"This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]","start":171784370,"end":171999859,"strand":-1,"description":"solute carrier family 25 member 12 [Source:HGNC Symbol;Acc:HGNC:10982]"}, {"versioned_ensembl_gene_id":"ENSG00000265943.1","gene_symbol":"AC090912.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22699481,"end":22933764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271065.1","gene_symbol":"AC107031.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51421956,"end":51424611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142556.18","gene_symbol":"ZNF614","gene_name":"zinc finger protein 614 [Source:HGNC Symbol;Acc:HGNC:24722]","synonyms":"FLJ21941","biotype":"protein_coding","ncbi_id":"80110","summary":null,"start":52012765,"end":52030240,"strand":-1,"description":"zinc finger protein 614 [Source:HGNC Symbol;Acc:HGNC:24722]"}, {"versioned_ensembl_gene_id":"ENSG00000184261.4","gene_symbol":"KCNK12","gene_name":"potassium two pore domain channel subfamily K member 12 [Source:HGNC Symbol;Acc:HGNC:6274]","synonyms":"K2p12.1,THIK2,THIK-2","biotype":"protein_coding","ncbi_id":"56660","summary":"This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008]","start":47516581,"end":47570939,"strand":-1,"description":"potassium two pore domain channel subfamily K member 12 [Source:HGNC Symbol;Acc:HGNC:6274]"}, {"versioned_ensembl_gene_id":"ENSG00000264488.1","gene_symbol":"AC090283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40803744,"end":40809296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268101.2","gene_symbol":"CYP2G2P","gene_name":"cytochrome P450 family 2 subfamily G member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:15653]","synonyms":"CYP2GP2,CYP2G2","biotype":"unprocessed_pseudogene","ncbi_id":"83757","summary":null,"start":41050449,"end":41062444,"strand":-1,"description":"cytochrome P450 family 2 subfamily G member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:15653]"}, {"versioned_ensembl_gene_id":"ENSG00000221996.6","gene_symbol":"OR52B4","gene_name":"olfactory receptor family 52 subfamily B member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15209]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"143496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":4367263,"end":4368386,"strand":-1,"description":"olfactory receptor family 52 subfamily B member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15209]"}, {"versioned_ensembl_gene_id":"ENSG00000282709.1","gene_symbol":"TRBV7-5","gene_name":"T-cell receptor beta variable 7-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12239]","synonyms":"TRBV75,TCRBV7S5,TCRBV6S9P","biotype":"TR_V_pseudogene","ncbi_id":"28593","summary":null,"start":142495814,"end":142496285,"strand":1,"description":"T-cell receptor beta variable 7-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12239]"}, {"versioned_ensembl_gene_id":"ENSG00000257613.1","gene_symbol":"LINC01481","gene_name":"long intergenic non-protein coding RNA 1481 [Source:HGNC Symbol;Acc:HGNC:51126]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928062","summary":null,"start":70219132,"end":70221862,"strand":-1,"description":"long intergenic non-protein coding RNA 1481 [Source:HGNC Symbol;Acc:HGNC:51126]"}, {"versioned_ensembl_gene_id":"ENSG00000258278.2","gene_symbol":"CLUHP8","gene_name":"clustered mitochondria homolog pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51573]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418733","summary":null,"start":38082046,"end":38087392,"strand":1,"description":"clustered mitochondria homolog pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51573]"}, {"versioned_ensembl_gene_id":"ENSG00000126467.10","gene_symbol":"TSKS","gene_name":"testis specific serine kinase substrate [Source:HGNC Symbol;Acc:HGNC:30719]","synonyms":"TSSKS,PPP1R161","biotype":"protein_coding","ncbi_id":"60385","summary":"This gene may play a role in testicular physiology, spermatogenesis or spermiogenesis. Expression of the encoded protein is highest in the testis and down-regulated in testicular cancer. The gene is localized to the region 19q13.3 among the related RAS viral oncogene homolog (RRAS) and interferon regulatory factor 3 (IRF3) genes, which are both involved in tumorigenesis pathways and progression. [provided by RefSeq, Jul 2008]","start":49739753,"end":49763330,"strand":-1,"description":"testis specific serine kinase substrate [Source:HGNC Symbol;Acc:HGNC:30719]"}, {"versioned_ensembl_gene_id":"ENSG00000258794.3","gene_symbol":"DUX4L27","gene_name":"double homeobox 4 like 27 [Source:HGNC Symbol;Acc:HGNC:50808]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131369","summary":null,"start":34208415,"end":34209675,"strand":-1,"description":"double homeobox 4 like 27 [Source:HGNC Symbol;Acc:HGNC:50808]"}, {"versioned_ensembl_gene_id":"ENSG00000215881.3","gene_symbol":"LINC02337","gene_name":"long intergenic non-protein coding RNA 2337 [Source:HGNC Symbol;Acc:HGNC:53257]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370369","summary":null,"start":111596009,"end":111642079,"strand":1,"description":"long intergenic non-protein coding RNA 2337 [Source:HGNC Symbol;Acc:HGNC:53257]"}, {"versioned_ensembl_gene_id":"ENSG00000135040.15","gene_symbol":"NAA35","gene_name":"N(alpha)-acetyltransferase 35, NatC auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:24340]","synonyms":"MAK10,FLJ22643,FLJ21613,bA379P1.1","biotype":"protein_coding","ncbi_id":"60560","summary":null,"start":85941146,"end":86022298,"strand":1,"description":"N(alpha)-acetyltransferase 35, NatC auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:24340]"}, {"versioned_ensembl_gene_id":"ENSG00000165028.11","gene_symbol":"NIPSNAP3B","gene_name":"nipsnap homolog 3B [Source:HGNC Symbol;Acc:HGNC:23641]","synonyms":"FLJ11275","biotype":"protein_coding","ncbi_id":"55335","summary":"NIPSNAP3B belongs to a family of proteins with putative roles in vesicular trafficking (Buechler et al., 2004 [PubMed 15177564]).[supplied by OMIM, Mar 2008]","start":104764157,"end":104777457,"strand":1,"description":"nipsnap homolog 3B [Source:HGNC Symbol;Acc:HGNC:23641]"}, {"versioned_ensembl_gene_id":"ENSG00000228625.1","gene_symbol":"AL451047.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":227178333,"end":227183444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166741.7","gene_symbol":"NNMT","gene_name":"nicotinamide N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:7861]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4837","summary":"N-methylation is one method by which drug and other xenobiotic compounds are metabolized by the liver. This gene encodes the protein responsible for this enzymatic activity which uses S-adenosyl methionine as the methyl donor. [provided by RefSeq, Jul 2008]","start":114257787,"end":114313285,"strand":1,"description":"nicotinamide N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:7861]"}, {"versioned_ensembl_gene_id":"ENSG00000264825.1","gene_symbol":"AC091588.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22213778,"end":22228029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160446.18","gene_symbol":"ZDHHC12","gene_name":"zinc finger DHHC-type containing 12 [Source:HGNC Symbol;Acc:HGNC:19159]","synonyms":"ZNF400,FLJ14524","biotype":"protein_coding","ncbi_id":"84885","summary":null,"start":128720869,"end":128724127,"strand":-1,"description":"zinc finger DHHC-type containing 12 [Source:HGNC Symbol;Acc:HGNC:19159]"}, {"versioned_ensembl_gene_id":"ENSG00000257629.1","gene_symbol":"AC006199.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89027757,"end":89028522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204449.3","gene_symbol":"TRIM49C","gene_name":"tripartite motif containing 49C [Source:HGNC Symbol;Acc:HGNC:38877]","synonyms":"TRIM49L2","biotype":"protein_coding","ncbi_id":"642612","summary":null,"start":90031106,"end":90042025,"strand":1,"description":"tripartite motif containing 49C [Source:HGNC Symbol;Acc:HGNC:38877]"}, {"versioned_ensembl_gene_id":"ENSG00000253811.1","gene_symbol":"AC136424.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158983006,"end":158984789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253228.1","gene_symbol":"NRBF2P4","gene_name":"nuclear receptor binding factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44607]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728381","summary":null,"start":107983116,"end":107983965,"strand":1,"description":"nuclear receptor binding factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44607]"}, {"versioned_ensembl_gene_id":"ENSG00000264548.1","gene_symbol":"AC132872.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82214227,"end":82217352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265678.1","gene_symbol":"AC129510.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82153430,"end":82154815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228206.2","gene_symbol":"AC016717.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":225698254,"end":225698539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101605.12","gene_symbol":"MYOM1","gene_name":"myomesin 1 [Source:HGNC Symbol;Acc:HGNC:7613]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8736","summary":"The giant protein titin, together with its associated proteins, interconnects the major structure of sarcomeres, the M bands and Z discs. The C-terminal end of the titin string extends into the M line, where it binds tightly to M-band constituents of apparent molecular masses of 190 kD (myomesin 1) and 165 kD (myomesin 2). This protein, myomesin 1, like myomesin 2, titin, and other myofibrillar proteins contains structural modules with strong homology to either fibronectin type III (motif I) or immunoglobulin C2 (motif II) domains. Myomesin 1 and myomesin 2 each have a unique N-terminal region followed by 12 modules of motif I or motif II, in the arrangement II-II-I-I-I-I-I-II-II-II-II-II. The two proteins share 50% sequence identity in this repeat-containing region. The head structure formed by these 2 proteins on one end of the titin string extends into the center of the M band. The integrating structure of the sarcomere arises from muscle-specific members of the superfamily of immunoglobulin-like proteins. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":3066807,"end":3220108,"strand":-1,"description":"myomesin 1 [Source:HGNC Symbol;Acc:HGNC:7613]"}, {"versioned_ensembl_gene_id":"ENSG00000270781.1","gene_symbol":"AC091133.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48899131,"end":48899748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253626.3","gene_symbol":"EIF5AL1","gene_name":"eukaryotic translation initiation factor 5A-like 1 [Source:HGNC Symbol;Acc:HGNC:17419]","synonyms":"EIF5AP1,bA342M3.3","biotype":"protein_coding","ncbi_id":"143244","summary":null,"start":79512601,"end":79516440,"strand":1,"description":"eukaryotic translation initiation factor 5A-like 1 [Source:HGNC Symbol;Acc:HGNC:17419]"}, {"versioned_ensembl_gene_id":"ENSG00000226431.1","gene_symbol":"AL121929.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":103549075,"end":103550964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186665.9","gene_symbol":"C17orf58","gene_name":"chromosome 17 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:27568]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284018","summary":null,"start":67991101,"end":67996431,"strand":-1,"description":"chromosome 17 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:27568]"}, {"versioned_ensembl_gene_id":"ENSG00000148291.9","gene_symbol":"SURF2","gene_name":"surfeit 2 [Source:HGNC Symbol;Acc:HGNC:11475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6835","summary":"This gene shares a bidirectional promoter with surfeit 1 (SURF1; GeneID: 6834), which is located on the opposite strand. It encodes a conserved protein that is expressed in a variety of tissues. [provided by RefSeq, Jul 2013]","start":133356552,"end":133361169,"strand":1,"description":"surfeit 2 [Source:HGNC Symbol;Acc:HGNC:11475]"}, {"versioned_ensembl_gene_id":"ENSG00000279443.1","gene_symbol":"AL513497.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":28544460,"end":28546542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214890.3","gene_symbol":"AC020937.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79000112,"end":79001124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237706.4","gene_symbol":"TRIM51EP","gene_name":"tripartite motif-containing 51E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43970]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"399940","summary":null,"start":89981441,"end":89989559,"strand":-1,"description":"tripartite motif-containing 51E, pseudogene [Source:HGNC Symbol;Acc:HGNC:43970]"}, {"versioned_ensembl_gene_id":"ENSG00000236136.1","gene_symbol":"ADORA2BP1","gene_name":"adenosine A2b receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:265]","synonyms":"ADORA2BP","biotype":"processed_pseudogene","ncbi_id":"137","summary":null,"start":209744373,"end":209745214,"strand":1,"description":"adenosine A2b receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:265]"}, {"versioned_ensembl_gene_id":"ENSG00000205240.4","gene_symbol":"OR7E36P","gene_name":"olfactory receptor family 7 subfamily E member 36 pseudogene [Source:HGNC Symbol;Acc:HGNC:8409]","synonyms":"OST024,OR7E119P","biotype":"unprocessed_pseudogene","ncbi_id":"26637","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":41431248,"end":41432201,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 36 pseudogene [Source:HGNC Symbol;Acc:HGNC:8409]"}, {"versioned_ensembl_gene_id":"ENSG00000133818.13","gene_symbol":"RRAS2","gene_name":"related RAS viral (r-ras) oncogene homolog 2 [Source:HGNC Symbol;Acc:HGNC:17271]","synonyms":"TC21","biotype":"protein_coding","ncbi_id":"22800","summary":"This gene encodes a member of the R-Ras subfamily of Ras-like small GTPases. The encoded protein associates with the plasma membrane and may function as a signal transducer. This protein may play an important role in activating signal transduction pathways that control cell proliferation. Mutations in this gene are associated with the growth of certain tumors. Pseudogenes of this gene are found on chromosomes 1 and 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":14277926,"end":14364506,"strand":-1,"description":"related RAS viral (r-ras) oncogene homolog 2 [Source:HGNC Symbol;Acc:HGNC:17271]"}, {"versioned_ensembl_gene_id":"ENSG00000226384.10","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFIIH,TFB2,P52","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30898895,"end":30904817,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000255235.1","gene_symbol":"AP005435.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89883927,"end":89886213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266717.1","gene_symbol":"AC134407.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67950885,"end":67951746,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178591.6","gene_symbol":"DEFB125","gene_name":"defensin beta 125 [Source:HGNC Symbol;Acc:HGNC:18105]","synonyms":"DEFB-25","biotype":"protein_coding","ncbi_id":"245938","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the host immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20p13. [provided by RefSeq, Nov 2014]","start":87250,"end":97094,"strand":1,"description":"defensin beta 125 [Source:HGNC Symbol;Acc:HGNC:18105]"}, {"versioned_ensembl_gene_id":"ENSG00000279880.1","gene_symbol":"AC134407.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67973934,"end":67976072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198863.7","gene_symbol":"RUNDC1","gene_name":"RUN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25418]","synonyms":"DKFZp761H0421","biotype":"protein_coding","ncbi_id":"146923","summary":"This gene encodes a protein that contains a RUN (RPIP8, UNC-14 and NESCA) domain and a coiled coil domain. The encoded protein may negatively regulate p53 transcriptional activity. This gene is a potential candidate gene for predisposition to glioma in humans. [provided by RefSeq, May 2017]","start":42980565,"end":42993690,"strand":1,"description":"RUN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25418]"}, {"versioned_ensembl_gene_id":"ENSG00000214559.3","gene_symbol":"AC019077.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98251688,"end":98261630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280131.1","gene_symbol":"AC027348.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49711273,"end":49711914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233692.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31916635,"end":31923909,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000256671.6","gene_symbol":"LIMS4","gene_name":"LIM zinc finger domain containing 4 [Source:HGNC Symbol;Acc:HGNC:39941]","synonyms":"LIMS3L","biotype":"protein_coding","ncbi_id":"100288695","summary":null,"start":110446640,"end":110473075,"strand":-1,"description":"LIM zinc finger domain containing 4 [Source:HGNC Symbol;Acc:HGNC:39941]"}, {"versioned_ensembl_gene_id":"ENSG00000273471.1","gene_symbol":"AC112229.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":110386411,"end":110433673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232997.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"dJ111M5.3,ZNF463P","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28889708,"end":28890782,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000280083.1","gene_symbol":"AC079777.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":191154118,"end":191156070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151892.14","gene_symbol":"GFRA1","gene_name":"GDNF family receptor alpha 1 [Source:HGNC Symbol;Acc:HGNC:4243]","synonyms":"GDNFRA,GDNFR,TRNR1,RETL1,RET1L,GFR-ALPHA-1","biotype":"protein_coding","ncbi_id":"2674","summary":"This gene encodes a member of the glial cell line-derived neurotrophic factor receptor (GDNFR) family of proteins. The encoded preproprotein is proteolytically processed to generate the mature receptor. Glial cell line-derived neurotrophic factor (GDNF) and neurturin (NTN) are two structurally related, potent neurotrophic factors that play key roles in the control of neuron survival and differentiation. This receptor is a glycosylphosphatidylinositol (GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor. This gene is a candidate gene for Hirschsprung disease. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":116056925,"end":116273467,"strand":-1,"description":"GDNF family receptor alpha 1 [Source:HGNC Symbol;Acc:HGNC:4243]"}, {"versioned_ensembl_gene_id":"ENSG00000170264.12","gene_symbol":"FAM161A","gene_name":"family with sequence similarity 161 member A [Source:HGNC Symbol;Acc:HGNC:25808]","synonyms":"RP28,FLJ13305","biotype":"protein_coding","ncbi_id":"84140","summary":"This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]","start":61824854,"end":61854143,"strand":-1,"description":"family with sequence similarity 161 member A [Source:HGNC Symbol;Acc:HGNC:25808]"}, {"versioned_ensembl_gene_id":"ENSG00000251647.2","gene_symbol":"AC114781.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83377363,"end":83378076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182963.9","gene_symbol":"GJC1","gene_name":"gap junction protein gamma 1 [Source:HGNC Symbol;Acc:HGNC:4280]","synonyms":"GJA7,CX45","biotype":"protein_coding","ncbi_id":"10052","summary":"This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Alternatively spliced transcript variants encoding the same isoform have been described. [provided by RefSeq, Jul 2008]","start":44798448,"end":44830816,"strand":-1,"description":"gap junction protein gamma 1 [Source:HGNC Symbol;Acc:HGNC:4280]"}, {"versioned_ensembl_gene_id":"ENSG00000242849.2","gene_symbol":"ALDOAP1","gene_name":"aldolase, fructose-bisphosphate A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:415]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391538","summary":null,"start":52193170,"end":52194785,"strand":1,"description":"aldolase, fructose-bisphosphate A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:415]"}, {"versioned_ensembl_gene_id":"ENSG00000236636.2","gene_symbol":"AL627308.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":227264776,"end":227265207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281477.1","gene_symbol":"LINC01955","gene_name":"long intergenic non-protein coding RNA 1955 [Source:HGNC Symbol;Acc:HGNC:52780]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374847","summary":null,"start":87249095,"end":87253750,"strand":-1,"description":"long intergenic non-protein coding RNA 1955 [Source:HGNC Symbol;Acc:HGNC:52780]"}, {"versioned_ensembl_gene_id":"ENSG00000233671.1","gene_symbol":"AC083899.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87221113,"end":87222488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235647.1","gene_symbol":"AL022319.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39750127,"end":39751293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197933.12","gene_symbol":"ZNF823","gene_name":"zinc finger protein 823 [Source:HGNC Symbol;Acc:HGNC:30936]","synonyms":"HSZFP36","biotype":"protein_coding","ncbi_id":"55552","summary":null,"start":11721265,"end":11739009,"strand":-1,"description":"zinc finger protein 823 [Source:HGNC Symbol;Acc:HGNC:30936]"}, {"versioned_ensembl_gene_id":"ENSG00000231163.5","gene_symbol":"CSMD2-AS1","gene_name":"CSMD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40882]","synonyms":"ENST00000434181","biotype":"antisense_RNA","ncbi_id":"402779","summary":null,"start":33868953,"end":33885458,"strand":1,"description":"CSMD2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40882]"}, {"versioned_ensembl_gene_id":"ENSG00000189184.11","gene_symbol":"PCDH18","gene_name":"protocadherin 18 [Source:HGNC Symbol;Acc:HGNC:14268]","synonyms":"PCDH68L,KIAA1562","biotype":"protein_coding","ncbi_id":"54510","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. This gene encodes a protein which contains 6 extracellular cadherin domains, a transmembrane domain and a cytoplasmic tail differing from those of the classical cadherins. Although its specific function is undetermined, the cadherin-related neuronal receptor is thought to play a role in the establishment and function of specific cell-cell connections in the brain. [provided by RefSeq, Jul 2008]","start":137518918,"end":137532494,"strand":-1,"description":"protocadherin 18 [Source:HGNC Symbol;Acc:HGNC:14268]"}, {"versioned_ensembl_gene_id":"ENSG00000267343.2","gene_symbol":"ZNF833P","gene_name":"zinc finger protein 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:33819]","synonyms":"ZNF833","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401898","summary":null,"start":11680944,"end":11686259,"strand":1,"description":"zinc finger protein 833, pseudogene [Source:HGNC Symbol;Acc:HGNC:33819]"}, {"versioned_ensembl_gene_id":"ENSG00000138085.16","gene_symbol":"ATRAID","gene_name":"all-trans retinoic acid induced differentiation factor [Source:HGNC Symbol;Acc:HGNC:24090]","synonyms":"C2orf28,APR3,p18,HSPC013","biotype":"protein_coding","ncbi_id":"51374","summary":"This gene is thought to be involved in apoptosis, and may also be involved in hematopoietic development and differentiation. The use of alternative splice sites and promotors result in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2009]","start":27212027,"end":27217178,"strand":1,"description":"all-trans retinoic acid induced differentiation factor [Source:HGNC Symbol;Acc:HGNC:24090]"}, {"versioned_ensembl_gene_id":"ENSG00000229653.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":29990518,"end":30051536,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000148303.16","gene_symbol":"RPL7A","gene_name":"ribosomal protein L7a [Source:HGNC Symbol;Acc:HGNC:10364]","synonyms":"TRUP,SURF3,L7A","biotype":"protein_coding","ncbi_id":"6130","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L7AE family of ribosomal proteins. It can interact with a subclass of nuclear hormone receptors, including thyroid hormone receptor, and inhibit their ability to transactivate by preventing their binding to their DNA response elements. This gene is included in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity. It is co-transcribed with the U24, U36a, U36b, and U36c small nucleolar RNA genes, which are located in its second, fifth, fourth, and sixth introns, respectively. This gene rearranges with the trk proto-oncogene to form the chimeric oncogene trk-2h, which encodes an oncoprotein consisting of the N terminus of ribosomal protein L7a fused to the receptor tyrosine kinase domain of trk. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":133348214,"end":133351426,"strand":1,"description":"ribosomal protein L7a [Source:HGNC Symbol;Acc:HGNC:10364]"}, {"versioned_ensembl_gene_id":"ENSG00000167178.15","gene_symbol":"ISLR2","gene_name":"immunoglobulin superfamily containing leucine rich repeat 2 [Source:HGNC Symbol;Acc:HGNC:29286]","synonyms":"KIAA1465","biotype":"protein_coding","ncbi_id":"57611","summary":null,"start":74100311,"end":74138540,"strand":1,"description":"immunoglobulin superfamily containing leucine rich repeat 2 [Source:HGNC Symbol;Acc:HGNC:29286]"}, {"versioned_ensembl_gene_id":"ENSG00000242768.2","gene_symbol":"AC096576.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21656511,"end":21656869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273849.1","gene_symbol":"SDR42E1P4","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51835]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422348","summary":null,"start":66724584,"end":66725064,"strand":1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51835]"}, {"versioned_ensembl_gene_id":"ENSG00000280650.1","gene_symbol":"KCNIP4-IT1","gene_name":"KCNIP4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:29895]","synonyms":"UM9-5,NCRNA00099","biotype":"lincRNA","ncbi_id":"359822","summary":null,"start":21843341,"end":21853188,"strand":-1,"description":"KCNIP4 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:29895]"}, {"versioned_ensembl_gene_id":"ENSG00000233683.1","gene_symbol":"AC004965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101388868,"end":101389080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196655.11","gene_symbol":"TRAPPC4","gene_name":"trafficking protein particle complex 4 [Source:HGNC Symbol;Acc:HGNC:19943]","synonyms":"SBDN,PTD009,TRS23","biotype":"protein_coding","ncbi_id":"51399","summary":null,"start":119018432,"end":119025454,"strand":1,"description":"trafficking protein particle complex 4 [Source:HGNC Symbol;Acc:HGNC:19943]"}, {"versioned_ensembl_gene_id":"ENSG00000218351.2","gene_symbol":"RPS3AP23","gene_name":"ribosomal protein S3a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36767]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271131","summary":null,"start":141635650,"end":141636503,"strand":-1,"description":"ribosomal protein S3a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36767]"}, {"versioned_ensembl_gene_id":"ENSG00000215357.2","gene_symbol":"HSPD1P8","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35145]","synonyms":"HSPD1-12P","biotype":"processed_pseudogene","ncbi_id":"647298","summary":null,"start":78849231,"end":78851208,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35145]"}, {"versioned_ensembl_gene_id":"ENSG00000236764.4","gene_symbol":"COX7A2P2","gene_name":"cytochrome c oxidase subunit 7A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2290]","synonyms":"COX7AP2,COX7AL2,COX7A3","biotype":"processed_pseudogene","ncbi_id":"1348","summary":null,"start":96902801,"end":96903050,"strand":1,"description":"cytochrome c oxidase subunit 7A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2290]"}, {"versioned_ensembl_gene_id":"ENSG00000227514.3","gene_symbol":"AC107890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113376669,"end":113377227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261659.2","gene_symbol":"Z92544.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":689001,"end":692554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270828.1","gene_symbol":"AL023806.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145736911,"end":145737173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081138.13","gene_symbol":"CDH7","gene_name":"cadherin 7 [Source:HGNC Symbol;Acc:HGNC:1766]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1005","summary":"This gene encodes a type II classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium dependent cell-cell adhesion molecule is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Type II (atypical) cadherins are defined based on their lack of a histidine-alanine-valine (HAV) cell adhesion recognition sequence specific to type I cadherins. Cadherins mediate cell-cell binding in a homophilic manner, contributing to the sorting of heterogeneous cell types. Mutations in this gene may be associated with bipolar disease in human patients. This gene is present in a gene cluster on chromosome 18. [provided by RefSeq, May 2016]","start":65750252,"end":65890341,"strand":1,"description":"cadherin 7 [Source:HGNC Symbol;Acc:HGNC:1766]"}, {"versioned_ensembl_gene_id":"ENSG00000014914.20","gene_symbol":"MTMR11","gene_name":"myotubularin related protein 11 [Source:HGNC Symbol;Acc:HGNC:24307]","synonyms":"CRA","biotype":"protein_coding","ncbi_id":"10903","summary":null,"start":149928651,"end":149936869,"strand":-1,"description":"myotubularin related protein 11 [Source:HGNC Symbol;Acc:HGNC:24307]"}, {"versioned_ensembl_gene_id":"ENSG00000263720.1","gene_symbol":"AC023394.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65865262,"end":65866397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259046.1","gene_symbol":"AL049870.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44888556,"end":44889041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211867.1","gene_symbol":"TRAJ22","gene_name":"T-cell receptor alpha joining 22 [Source:HGNC Symbol;Acc:HGNC:12051]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28733","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22522040,"end":22522102,"strand":1,"description":"T-cell receptor alpha joining 22 [Source:HGNC Symbol;Acc:HGNC:12051]"}, {"versioned_ensembl_gene_id":"ENSG00000280515.1","gene_symbol":"SALRNA2","gene_name":"senescence associated long non-coding RNA 2 [Source:NCBI gene;Acc:104548973]","synonyms":"XLOC_025931,SAL-RNA2","biotype":"lincRNA","ncbi_id":"104548973","summary":null,"start":70635249,"end":70637314,"strand":1,"description":"senescence associated long non-coding RNA 2 [Source:NCBI gene;Acc:104548973]"}, {"versioned_ensembl_gene_id":"ENSG00000281264.1","gene_symbol":"SALRNA3","gene_name":"senescence associated long non-coding RNA 3 [Source:NCBI gene;Acc:104548972]","synonyms":"XLOC_025918,SAL-RNA3","biotype":"lincRNA","ncbi_id":"104548972","summary":null,"start":70615547,"end":70616567,"strand":1,"description":"senescence associated long non-coding RNA 3 [Source:NCBI gene;Acc:104548972]"}, {"versioned_ensembl_gene_id":"ENSG00000118181.10","gene_symbol":"RPS25","gene_name":"ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:10413]","synonyms":"S25","biotype":"protein_coding","ncbi_id":"6230","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S25E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":119015712,"end":119018691,"strand":-1,"description":"ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:10413]"}, {"versioned_ensembl_gene_id":"ENSG00000134262.12","gene_symbol":"AP4B1","gene_name":"adaptor related protein complex 4 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:572]","synonyms":"BETA-4,SPG47","biotype":"protein_coding","ncbi_id":"10717","summary":"This gene encodes a subunit of a heterotetrameric adapter-like complex 4 that is involved in targeting proteins from the trans-Golgi network to the endosomal-lysosomal system. Mutations in this gene are associated with cerebral palsy spastic quadriplegic type 5 (CPSQ5) disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":113894748,"end":113905201,"strand":-1,"description":"adaptor related protein complex 4 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:572]"}, {"versioned_ensembl_gene_id":"ENSG00000211864.2","gene_symbol":"TRAJ25","gene_name":"T-cell receptor alpha joining 25 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12054]","synonyms":null,"biotype":"TR_J_gene","ncbi_id":"28730","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22518812,"end":22518871,"strand":1,"description":"T-cell receptor alpha joining 25 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12054]"}, {"versioned_ensembl_gene_id":"ENSG00000255385.1","gene_symbol":"UBTFL10","gene_name":"upstream binding transcription factor, RNA polymerase I-like 10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50287]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480293","summary":null,"start":89700764,"end":89701325,"strand":1,"description":"upstream binding transcription factor, RNA polymerase I-like 10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50287]"}, {"versioned_ensembl_gene_id":"ENSG00000254216.1","gene_symbol":"AC107952.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56252960,"end":56253372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263257.1","gene_symbol":"AC040173.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14408039,"end":14418872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279056.1","gene_symbol":"AP003400.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89556860,"end":89557205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133243.8","gene_symbol":"BTBD2","gene_name":"BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15504]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55643","summary":"The C-terminus of the protein encoded by this gene binds topoisomerase I. The N-terminus contains a proline-rich region and a BTB/POZ domain (broad-complex, Tramtrack and bric a brac/Pox virus and Zinc finger), both of which are typically involved in protein-protein interactions. Subcellularly, the protein localizes to cytoplasmic bodies. [provided by RefSeq, Jul 2008]","start":1985438,"end":2034881,"strand":-1,"description":"BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15504]"}, {"versioned_ensembl_gene_id":"ENSG00000181938.13","gene_symbol":"GINS3","gene_name":"GINS complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25851]","synonyms":"PSF3,FLJ13912","biotype":"protein_coding","ncbi_id":"64785","summary":"This gene encodes a protein subunit of the GINS heterotetrameric complex, which is essential for the initiation of DNA replication and replisome progression in eukaryotes. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":58295080,"end":58406144,"strand":1,"description":"GINS complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25851]"}, {"versioned_ensembl_gene_id":"ENSG00000113716.12","gene_symbol":"HMGXB3","gene_name":"HMG-box containing 3 [Source:HGNC Symbol;Acc:HGNC:28982]","synonyms":"SMF,KIAA0194,HMGX3","biotype":"protein_coding","ncbi_id":"22993","summary":"This gene is one of the non-canonical high mobility group (HMG) genes. The encoded protein contains an HMG-box domain found in DNA binding proteins such as transcription factors and chromosomal proteins. [provided by RefSeq, Aug 2011]","start":150000046,"end":150053142,"strand":1,"description":"HMG-box containing 3 [Source:HGNC Symbol;Acc:HGNC:28982]"}, {"versioned_ensembl_gene_id":"ENSG00000251508.1","gene_symbol":"AL133380.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":233295325,"end":233295727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268858.2","gene_symbol":"AL118506.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63861212,"end":63864293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142002.16","gene_symbol":"DPP9","gene_name":"dipeptidyl peptidase 9 [Source:HGNC Symbol;Acc:HGNC:18648]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91039","summary":"This gene encodes a protein that is a member of the S9B family in clan SC of the serine proteases. The protein has been shown to have post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Although the activity of this protein is similar to that of dipeptidyl peptidase 4 (DPP4), it does not appear to be membrane bound. In general, dipeptidyl peptidases appear to be involved in the regulation of the activity of their substrates and have been linked to a variety of diseases including type 2 diabetes, obesity and cancer. Several transcript variants of this gene have been described but not fully characterized. [provided by RefSeq, Jul 2008]","start":4675224,"end":4724673,"strand":-1,"description":"dipeptidyl peptidase 9 [Source:HGNC Symbol;Acc:HGNC:18648]"}, {"versioned_ensembl_gene_id":"ENSG00000256502.1","gene_symbol":"AC073913.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127344258,"end":127344402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228446.2","gene_symbol":"AC073052.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224499387,"end":224500100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269547.1","gene_symbol":"AC011455.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38915404,"end":38949855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235050.6","gene_symbol":"MLIP-AS1","gene_name":"MLIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40963]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873951","summary":null,"start":53978549,"end":54079726,"strand":-1,"description":"MLIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40963]"}, {"versioned_ensembl_gene_id":"ENSG00000231690.2","gene_symbol":"LINC00574","gene_name":"long intergenic non-protein coding RNA 574 [Source:HGNC Symbol;Acc:HGNC:21598]","synonyms":"FLJ13162,dJ182D15.1,C6orf208","biotype":"lincRNA","ncbi_id":"80069","summary":null,"start":169790321,"end":169802873,"strand":1,"description":"long intergenic non-protein coding RNA 574 [Source:HGNC Symbol;Acc:HGNC:21598]"}, {"versioned_ensembl_gene_id":"ENSG00000176909.11","gene_symbol":"MAMSTR","gene_name":"MEF2 activating motif and SAP domain containing transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:26689]","synonyms":"FLJ36070,MASTR","biotype":"protein_coding","ncbi_id":"284358","summary":null,"start":48712742,"end":48719721,"strand":-1,"description":"MEF2 activating motif and SAP domain containing transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:26689]"}, {"versioned_ensembl_gene_id":"ENSG00000269858.5","gene_symbol":"EGLN2","gene_name":"egl-9 family hypoxia inducible factor 2 [Source:HGNC Symbol;Acc:HGNC:14660]","synonyms":"PHD1,HIFPH1","biotype":"protein_coding","ncbi_id":"112398","summary":"The hypoxia inducible factor (HIF) is a transcriptional complex that is involved in oxygen homeostasis. At normal oxygen levels, the alpha subunit of HIF is targeted for degration by prolyl hydroxylation. This gene encodes an enzyme responsible for this post-translational modification. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream RAB4B (RAB4B, member RAS oncogene family) gene. [provided by RefSeq, Feb 2011]","start":40798996,"end":40808433,"strand":1,"description":"egl-9 family hypoxia inducible factor 2 [Source:HGNC Symbol;Acc:HGNC:14660]"}, {"versioned_ensembl_gene_id":"ENSG00000280604.1","gene_symbol":"AJ239328.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":45914296,"end":45919483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096150.9","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"KE-3,S18,HKE3,KE3,D6S218E","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33200834,"end":33205337,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000228717.1","gene_symbol":"AF013593.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151226229,"end":151227715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105991.7","gene_symbol":"HOXA1","gene_name":"homeobox A1 [Source:HGNC Symbol;Acc:HGNC:5099]","synonyms":"HOX1F,HOX1","biotype":"protein_coding","ncbi_id":"3198","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. The encoded protein may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development. Two transcript variants encoding two different isoforms have been found for this gene, with only one of the isoforms containing the homeodomain region. [provided by RefSeq, Jul 2008]","start":27092993,"end":27095996,"strand":-1,"description":"homeobox A1 [Source:HGNC Symbol;Acc:HGNC:5099]"}, {"versioned_ensembl_gene_id":"ENSG00000182795.12","gene_symbol":"C1orf116","gene_name":"chromosome 1 open reading frame 116 [Source:HGNC Symbol;Acc:HGNC:28667]","synonyms":"SARG,MGC4309,MGC2742,FLJ36507","biotype":"protein_coding","ncbi_id":"79098","summary":null,"start":207018521,"end":207032756,"strand":-1,"description":"chromosome 1 open reading frame 116 [Source:HGNC Symbol;Acc:HGNC:28667]"}, {"versioned_ensembl_gene_id":"ENSG00000237063.1","gene_symbol":"AL035420.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36086252,"end":36088192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242510.1","gene_symbol":"NDUFB4P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288654","summary":null,"start":67513940,"end":67514320,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45248]"}, {"versioned_ensembl_gene_id":"ENSG00000067533.5","gene_symbol":"RRP15","gene_name":"ribosomal RNA processing 15 homolog [Source:HGNC Symbol;Acc:HGNC:24255]","synonyms":"KIAA0507,CGI-115","biotype":"protein_coding","ncbi_id":"51018","summary":"This gene encodes a protein that co-purifies with human nucleoli. A similar protein in budding yeast is a component of pre-60S ribosomal particles, and is required for the early maturation steps of the 60S subunit. [provided by RefSeq, Jul 2008]","start":218285287,"end":218337983,"strand":1,"description":"ribosomal RNA processing 15 homolog [Source:HGNC Symbol;Acc:HGNC:24255]"}, {"versioned_ensembl_gene_id":"ENSG00000171051.8","gene_symbol":"FPR1","gene_name":"formyl peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:3826]","synonyms":"FPR,FMLP","biotype":"protein_coding","ncbi_id":"2357","summary":"This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.[provided by RefSeq, Jul 2010]","start":51745172,"end":51804110,"strand":-1,"description":"formyl peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:3826]"}, {"versioned_ensembl_gene_id":"ENSG00000273668.1","gene_symbol":"AL136317.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":66017643,"end":66017868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227056.2","gene_symbol":"RPL6P2","gene_name":"ribosomal protein L6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35964]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343495","summary":null,"start":119219314,"end":119220096,"strand":-1,"description":"ribosomal protein L6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35964]"}, {"versioned_ensembl_gene_id":"ENSG00000225208.1","gene_symbol":"AL133387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101311018,"end":101311505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228467.2","gene_symbol":"AL845311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38804007,"end":38851916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258945.1","gene_symbol":"AL049775.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85528599,"end":85529386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271712.1","gene_symbol":"AL163642.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84998278,"end":84999296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258506.2","gene_symbol":"AL163642.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84951274,"end":84951373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274495.1","gene_symbol":"LENG9","gene_name":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94059","summary":null,"start":54392112,"end":54394035,"strand":-1,"description":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]"}, {"versioned_ensembl_gene_id":"ENSG00000278116.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5.1,KIR2DL5,KIR2DL5,CD158F,KIR2DL5.1,CD158F","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877311,"end":54886807,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000164082.14","gene_symbol":"GRM2","gene_name":"glutamate metabotropic receptor 2 [Source:HGNC Symbol;Acc:HGNC:4594]","synonyms":"MGLUR2,mGlu2,GPRC1B","biotype":"protein_coding","ncbi_id":"2912","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2017]","start":51707070,"end":51718613,"strand":1,"description":"glutamate metabotropic receptor 2 [Source:HGNC Symbol;Acc:HGNC:4594]"}, {"versioned_ensembl_gene_id":"ENSG00000229274.1","gene_symbol":"AL662860.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29497509,"end":29510556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234102.1","gene_symbol":"KRT19P4","gene_name":"keratin 19 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45073]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128041","summary":null,"start":68260557,"end":68261499,"strand":1,"description":"keratin 19 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45073]"}, {"versioned_ensembl_gene_id":"ENSG00000255860.3","gene_symbol":"AP000812.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72172455,"end":72177954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160683.4","gene_symbol":"CXCR5","gene_name":"C-X-C motif chemokine receptor 5 [Source:HGNC Symbol;Acc:HGNC:1060]","synonyms":"MDR15,CD185,BLR1","biotype":"protein_coding","ncbi_id":"643","summary":"This gene encodes a multi-pass membrane protein that belongs to the CXC chemokine receptor family. It is expressed in mature B-cells and Burkitt's lymphoma. This cytokine receptor binds to B-lymphocyte chemoattractant (BLC), and is involved in B-cell migration into B-cell follicles of spleen and Peyer patches. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":118883766,"end":118897799,"strand":1,"description":"C-X-C motif chemokine receptor 5 [Source:HGNC Symbol;Acc:HGNC:1060]"}, {"versioned_ensembl_gene_id":"ENSG00000282951.1","gene_symbol":"AC008537.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40779780,"end":40796943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229938.1","gene_symbol":"MYO16-AS2","gene_name":"MYO16 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39914]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874067","summary":null,"start":109101261,"end":109101919,"strand":-1,"description":"MYO16 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39914]"}, {"versioned_ensembl_gene_id":"ENSG00000121903.14","gene_symbol":"ZSCAN20","gene_name":"zinc finger and SCAN domain containing 20 [Source:HGNC Symbol;Acc:HGNC:13093]","synonyms":"ZNF360,ZNF31,KOX29","biotype":"protein_coding","ncbi_id":"7579","summary":null,"start":33472645,"end":33496507,"strand":1,"description":"zinc finger and SCAN domain containing 20 [Source:HGNC Symbol;Acc:HGNC:13093]"}, {"versioned_ensembl_gene_id":"ENSG00000225526.4","gene_symbol":"MKRN2OS","gene_name":"MKRN2 opposite strand [Source:HGNC Symbol;Acc:HGNC:40375]","synonyms":"MKRN2-AS1,C3orf83","biotype":"protein_coding","ncbi_id":"100129480","summary":null,"start":12514934,"end":12561059,"strand":-1,"description":"MKRN2 opposite strand [Source:HGNC Symbol;Acc:HGNC:40375]"}, {"versioned_ensembl_gene_id":"ENSG00000156374.14","gene_symbol":"PCGF6","gene_name":"polycomb group ring finger 6 [Source:HGNC Symbol;Acc:HGNC:21156]","synonyms":"RNF134,MBLR","biotype":"protein_coding","ncbi_id":"84108","summary":"The protein encoded by this gene contains a RING finger motif, which is most closely related to those of polycomb group (PcG) proteins RNF110/MEL-18 and BMI1. PcG proteins are known to form protein complexes and function as transcription repressors. This protein has been shown to interact with some PcG proteins and act as a transcription repressor. The activity of this protein is found to be regulated by cell cycle dependent phosphorylation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":103302796,"end":103351134,"strand":-1,"description":"polycomb group ring finger 6 [Source:HGNC Symbol;Acc:HGNC:21156]"}, {"versioned_ensembl_gene_id":"ENSG00000266088.5","gene_symbol":"AC004585.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40517026,"end":40527002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236668.2","gene_symbol":"AC006450.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124006277,"end":124009396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251413.1","gene_symbol":"AC068898.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48624004,"end":48625093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258418.1","gene_symbol":"AL352977.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40386252,"end":40386794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243003.3","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"NG32,C6orf21,LY6G6D,G6f","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31689056,"end":31692766,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000206427.11","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"G2,D6S51E,BAT2","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31610949,"end":31627996,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000183570.16","gene_symbol":"PCBP3","gene_name":"poly(rC) binding protein 3 [Source:HGNC Symbol;Acc:HGNC:8651]","synonyms":"PCBP3OT,PCBP3-OT1,FLJ44028","biotype":"protein_coding","ncbi_id":"54039","summary":"This gene encodes a member of the KH-domain protein subfamily. Proteins of this subfamily, also referred to as alpha-CPs, bind to RNA with a specificity for C-rich pyrimidine regions. Alpha-CPs play important roles in post-transcriptional activities and have different cellular distributions. The protein encoded by this gene lacks the nuclear localization signals found in other subfamily members. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2017]","start":45643694,"end":45942454,"strand":1,"description":"poly(rC) binding protein 3 [Source:HGNC Symbol;Acc:HGNC:8651]"}, {"versioned_ensembl_gene_id":"ENSG00000233602.1","gene_symbol":"ERI3-IT1","gene_name":"ERI3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41431]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874278","summary":null,"start":44243408,"end":44244273,"strand":-1,"description":"ERI3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41431]"}, {"versioned_ensembl_gene_id":"ENSG00000240842.1","gene_symbol":"AC099328.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69564106,"end":69571122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224554.2","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30530582,"end":30531232,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000227754.3","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"Em:AB014080.4,SUCLA2P","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30513524,"end":30514893,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000196968.10","gene_symbol":"FUT11","gene_name":"fucosyltransferase 11 [Source:HGNC Symbol;Acc:HGNC:19233]","synonyms":"MGC33202","biotype":"protein_coding","ncbi_id":"170384","summary":null,"start":73772291,"end":73780251,"strand":1,"description":"fucosyltransferase 11 [Source:HGNC Symbol;Acc:HGNC:19233]"}, {"versioned_ensembl_gene_id":"ENSG00000138798.11","gene_symbol":"EGF","gene_name":"epidermal growth factor [Source:HGNC Symbol;Acc:HGNC:3229]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1950","summary":"This gene encodes a member of the epidermal growth factor superfamily. The encoded preproprotein is proteolytically processed to generate the 53-amino acid epidermal growth factor peptide. This protein acts a potent mitogenic factor that plays an important role in the growth, proliferation and differentiation of numerous cell types. This protein acts by binding with high affinity to the cell surface receptor, epidermal growth factor receptor. Defects in this gene are the cause of hypomagnesemia type 4. Dysregulation of this gene has been associated with the growth and progression of certain cancers. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":109912884,"end":110012266,"strand":1,"description":"epidermal growth factor [Source:HGNC Symbol;Acc:HGNC:3229]"}, {"versioned_ensembl_gene_id":"ENSG00000138650.8","gene_symbol":"PCDH10","gene_name":"protocadherin 10 [Source:HGNC Symbol;Acc:HGNC:13404]","synonyms":"OL-PCDH,KIAA1400","biotype":"protein_coding","ncbi_id":"57575","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. This family member contains 6 extracellular cadherin domains, a transmembrane domain and a cytoplasmic tail differing from those of the classical cadherins. The encoded protein is a cadherin-related neuronal receptor thought to function in the establishment of specific cell-cell connections in the brain. This gene plays a role in inhibiting cancer cell motility and cell migration. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2015]","start":133149315,"end":133208606,"strand":1,"description":"protocadherin 10 [Source:HGNC Symbol;Acc:HGNC:13404]"}, {"versioned_ensembl_gene_id":"ENSG00000164284.14","gene_symbol":"GRPEL2","gene_name":"GrpE like 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21060]","synonyms":"Mt-GrpE#2,FLJ23713,DKFZp451C205","biotype":"protein_coding","ncbi_id":"134266","summary":null,"start":149345430,"end":149354583,"strand":1,"description":"GrpE like 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21060]"}, {"versioned_ensembl_gene_id":"ENSG00000087191.12","gene_symbol":"PSMC5","gene_name":"proteasome 26S subunit, ATPase 5 [Source:HGNC Symbol;Acc:HGNC:9552]","synonyms":"p45,TRIP1,TBP10,SUG1,SUG-1,S8,p45/SUG","biotype":"protein_coding","ncbi_id":"5705","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. In addition to participation in proteasome functions, this subunit may participate in transcriptional regulation since it has been shown to interact with the thyroid hormone receptor and retinoid X receptor-alpha. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":63827152,"end":63832026,"strand":1,"description":"proteasome 26S subunit, ATPase 5 [Source:HGNC Symbol;Acc:HGNC:9552]"}, {"versioned_ensembl_gene_id":"ENSG00000126698.10","gene_symbol":"DNAJC8","gene_name":"DnaJ heat shock protein family (Hsp40) member C8 [Source:HGNC Symbol;Acc:HGNC:15470]","synonyms":"SPF31","biotype":"protein_coding","ncbi_id":"22826","summary":null,"start":28199456,"end":28233025,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C8 [Source:HGNC Symbol;Acc:HGNC:15470]"}, {"versioned_ensembl_gene_id":"ENSG00000254415.3","gene_symbol":"SIGLEC14","gene_name":"sialic acid binding Ig like lectin 14 [Source:HGNC Symbol;Acc:HGNC:32926]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100049587","summary":null,"start":51642553,"end":51646801,"strand":-1,"description":"sialic acid binding Ig like lectin 14 [Source:HGNC Symbol;Acc:HGNC:32926]"}, {"versioned_ensembl_gene_id":"ENSG00000242841.1","gene_symbol":"KRT8P35","gene_name":"keratin 8 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39869]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418747","summary":null,"start":63096374,"end":63097711,"strand":-1,"description":"keratin 8 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39869]"}, {"versioned_ensembl_gene_id":"ENSG00000183718.5","gene_symbol":"TRIM52","gene_name":"tripartite motif containing 52 [Source:HGNC Symbol;Acc:HGNC:19024]","synonyms":"RNF102","biotype":"protein_coding","ncbi_id":"84851","summary":null,"start":181254417,"end":181261139,"strand":-1,"description":"tripartite motif containing 52 [Source:HGNC Symbol;Acc:HGNC:19024]"}, {"versioned_ensembl_gene_id":"ENSG00000260377.1","gene_symbol":"AC083801.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182739669,"end":182740848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244422.3","gene_symbol":"RPL38P3","gene_name":"ribosomal protein L38 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35980]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132311","summary":null,"start":54976159,"end":54976371,"strand":-1,"description":"ribosomal protein L38 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35980]"}, {"versioned_ensembl_gene_id":"ENSG00000282269.1","gene_symbol":"PRR4","gene_name":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]","synonyms":"PROL4,LPRP","biotype":"protein_coding","ncbi_id":"11272","summary":"This gene encodes a member of the proline-rich protein family that lacks a conserved repetitive domain. This protein may play a role in protective functions in the eye. Alternative splicing result in multiple transcript variants. Read-through transcription also exists between this gene and the upstream PRH1 (proline-rich protein HaeIII subfamily 1) gene. [provided by RefSeq, Feb 2011]","start":10845849,"end":11167847,"strand":-1,"description":"proline rich 4 (lacrimal) [Source:HGNC Symbol;Acc:HGNC:18020]"}, {"versioned_ensembl_gene_id":"ENSG00000244247.1","gene_symbol":"LINC01995","gene_name":"long intergenic non-protein coding RNA 1995 [Source:HGNC Symbol;Acc:HGNC:52828]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374244","summary":null,"start":182498264,"end":182507124,"strand":-1,"description":"long intergenic non-protein coding RNA 1995 [Source:HGNC Symbol;Acc:HGNC:52828]"}, {"versioned_ensembl_gene_id":"ENSG00000281450.1","gene_symbol":"PANDAR","gene_name":"promoter of CDKN1A antisense DNA damage activated RNA [Source:HGNC Symbol;Acc:HGNC:44048]","synonyms":"PANDA","biotype":"lincRNA","ncbi_id":"101154753","summary":"This gene produces a non-coding RNA that is thought to regulate the response to DNA damage. This gene is induced by tumor protein p53 and interacts with and modulates the activity of a transcription factor that induce pro-apoptotic genes. Deregulation of this gene is associated with cancer progression. [provided by RefSeq, Dec 2017]","start":36673621,"end":36675126,"strand":-1,"description":"promoter of CDKN1A antisense DNA damage activated RNA [Source:HGNC Symbol;Acc:HGNC:44048]"}, {"versioned_ensembl_gene_id":"ENSG00000143442.21","gene_symbol":"POGZ","gene_name":"pogo transposable element derived with ZNF domain [Source:HGNC Symbol;Acc:HGNC:18801]","synonyms":"ZNF280E,KIAA0461,ZNF635m","biotype":"protein_coding","ncbi_id":"23126","summary":"The protein encoded by this gene appears to be a zinc finger protein containing a transposase domain at the C-terminus. This protein was found to interact with the transcription factor SP1 in a yeast two-hybrid system. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Aug 2010]","start":151402724,"end":151459465,"strand":-1,"description":"pogo transposable element derived with ZNF domain [Source:HGNC Symbol;Acc:HGNC:18801]"}, {"versioned_ensembl_gene_id":"ENSG00000230426.2","gene_symbol":"ERVMER61-1","gene_name":"endogenous retrovirus group MER61 member 1 [Source:HGNC Symbol;Acc:HGNC:27919]","synonyms":"C1orf99","biotype":"lincRNA","ncbi_id":"339476","summary":null,"start":187641226,"end":187643860,"strand":1,"description":"endogenous retrovirus group MER61 member 1 [Source:HGNC Symbol;Acc:HGNC:27919]"}, {"versioned_ensembl_gene_id":"ENSG00000223441.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"HS6M1-14,OR2I2,OR2I4P,OR2I1,OR2I3P","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29552784,"end":29553731,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000197013.9","gene_symbol":"ZNF429","gene_name":"zinc finger protein 429 [Source:HGNC Symbol;Acc:HGNC:20817]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353088","summary":null,"start":21496682,"end":21556270,"strand":1,"description":"zinc finger protein 429 [Source:HGNC Symbol;Acc:HGNC:20817]"}, {"versioned_ensembl_gene_id":"ENSG00000270627.1","gene_symbol":"AL592221.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78589158,"end":78589539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206484.10","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30677568,"end":30680941,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000231164.1","gene_symbol":"RPL7P56","gene_name":"ribosomal protein L7 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728962","summary":null,"start":136791064,"end":136791780,"strand":1,"description":"ribosomal protein L7 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35588]"}, {"versioned_ensembl_gene_id":"ENSG00000123342.15","gene_symbol":"MMP19","gene_name":"matrix metallopeptidase 19 [Source:HGNC Symbol;Acc:HGNC:7165]","synonyms":"RASI-1,MMP18","biotype":"protein_coding","ncbi_id":"4327","summary":"This gene encodes a member of a family of proteins that are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded protein is secreted as an inactive proprotein, which is activated upon cleavage by extracellular proteases. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013]","start":55835433,"end":55842966,"strand":-1,"description":"matrix metallopeptidase 19 [Source:HGNC Symbol;Acc:HGNC:7165]"}, {"versioned_ensembl_gene_id":"ENSG00000101577.9","gene_symbol":"LPIN2","gene_name":"lipin 2 [Source:HGNC Symbol;Acc:HGNC:14450]","synonyms":"KIAA0249","biotype":"protein_coding","ncbi_id":"9663","summary":"Mouse studies suggest that this gene functions during normal adipose tissue development and may play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. [provided by RefSeq, Jul 2008]","start":2916994,"end":3013315,"strand":-1,"description":"lipin 2 [Source:HGNC Symbol;Acc:HGNC:14450]"}, {"versioned_ensembl_gene_id":"ENSG00000141449.14","gene_symbol":"GREB1L","gene_name":"growth regulation by estrogen in breast cancer 1 like [Source:HGNC Symbol;Acc:HGNC:31042]","synonyms":"FLJ13687,C18orf6,KIAA1772","biotype":"protein_coding","ncbi_id":"80000","summary":null,"start":21242242,"end":21525417,"strand":1,"description":"growth regulation by estrogen in breast cancer 1 like [Source:HGNC Symbol;Acc:HGNC:31042]"}, {"versioned_ensembl_gene_id":"ENSG00000229266.1","gene_symbol":"POM121L8P","gene_name":"POM121 transmembrane nucleoporin like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:35446]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"29797","summary":null,"start":21282881,"end":21284161,"strand":1,"description":"POM121 transmembrane nucleoporin like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:35446]"}, {"versioned_ensembl_gene_id":"ENSG00000234803.7","gene_symbol":"FAM197Y2","gene_name":"family with sequence similarity 197 Y-linked member 2 [Source:HGNC Symbol;Acc:HGNC:18848]","synonyms":"FAM197Y2P,CYorf16","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"252946","summary":null,"start":9517599,"end":9526897,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 2 [Source:HGNC Symbol;Acc:HGNC:18848]"}, {"versioned_ensembl_gene_id":"ENSG00000227500.9","gene_symbol":"SCAMP4","gene_name":"secretory carrier membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:30385]","synonyms":"FLJ33847","biotype":"protein_coding","ncbi_id":"113178","summary":"Secretory carrier membrane proteins (SCAMPs) are widely distributed integral membrane proteins implicated in membrane trafficking. Most SCAMPs (e.g., SCAMP1; MIM 606911) have N-terminal cytoplasmic NPF (arg-pro-phe) repeats, 4 central transmembrane regions, and a short C-terminal cytoplasmic tail. These SCAMPs likely have a role in endocytosis that is mediated by their NPF repeats. Other SCAMPs, such as SCAMP4, lack the NPF repeats and are therefore unlikely to function in endocytosis (summary by Fernandez-Chacon and Sudhof, 2000 [PubMed 11050114]).[supplied by OMIM, Feb 2011]","start":1905214,"end":1926013,"strand":1,"description":"secretory carrier membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:30385]"}, {"versioned_ensembl_gene_id":"ENSG00000143303.11","gene_symbol":"RRNAD1","gene_name":"ribosomal RNA adenine dimethylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24273]","synonyms":"C1orf66,METTL25B,CGI-41","biotype":"protein_coding","ncbi_id":"51093","summary":null,"start":156728442,"end":156736960,"strand":1,"description":"ribosomal RNA adenine dimethylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24273]"}, {"versioned_ensembl_gene_id":"ENSG00000153495.10","gene_symbol":"TEX29","gene_name":"testis expressed 29 [Source:HGNC Symbol;Acc:HGNC:20370]","synonyms":"MGC35169,C13orf16,bA474D23.1","biotype":"protein_coding","ncbi_id":"121793","summary":null,"start":111316184,"end":111344249,"strand":1,"description":"testis expressed 29 [Source:HGNC Symbol;Acc:HGNC:20370]"}, {"versioned_ensembl_gene_id":"ENSG00000151967.18","gene_symbol":"SCHIP1","gene_name":"schwannomin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:15678]","synonyms":"SCHIP-1","biotype":"protein_coding","ncbi_id":"29970","summary":null,"start":159839861,"end":159897360,"strand":1,"description":"schwannomin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:15678]"}, {"versioned_ensembl_gene_id":"ENSG00000225343.1","gene_symbol":"RPL21P66","gene_name":"ribosomal protein L21 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:36476]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271179","summary":null,"start":132518830,"end":132519295,"strand":-1,"description":"ribosomal protein L21 pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:36476]"}, {"versioned_ensembl_gene_id":"ENSG00000241211.1","gene_symbol":"IQCJ-SCHIP1-AS1","gene_name":"IQCJ-SCHIP1 readthrough antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41303]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874433","summary":null,"start":159765387,"end":159768612,"strand":-1,"description":"IQCJ-SCHIP1 readthrough antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41303]"}, {"versioned_ensembl_gene_id":"ENSG00000238186.1","gene_symbol":"AL603839.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40515754,"end":40517174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115947.13","gene_symbol":"ORC4","gene_name":"origin recognition complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:8490]","synonyms":"Orc4p,ORC4L,HsORC4","biotype":"protein_coding","ncbi_id":"5000","summary":"The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. This gene encodes a subunit of the ORC complex. Several alternatively spliced transcript variants, some of which encode the same protein, have been reported for this gene. [provided by RefSeq, Oct 2010]","start":147930397,"end":148021604,"strand":-1,"description":"origin recognition complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:8490]"}, {"versioned_ensembl_gene_id":"ENSG00000235725.1","gene_symbol":"AC007389.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65589566,"end":65640177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216937.13","gene_symbol":"CCDC7","gene_name":"coiled-coil domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26533]","synonyms":"FLJ32762,FLJ13031,C10orf68,BIOT2","biotype":"protein_coding","ncbi_id":"79741","summary":null,"start":32446140,"end":32882874,"strand":1,"description":"coiled-coil domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26533]"}, {"versioned_ensembl_gene_id":"ENSG00000204397.7","gene_symbol":"CARD16","gene_name":"caspase recruitment domain family member 16 [Source:HGNC Symbol;Acc:HGNC:33701]","synonyms":"PSEUDO-ICE,COP1,COP","biotype":"protein_coding","ncbi_id":"114769","summary":null,"start":105041326,"end":105101431,"strand":-1,"description":"caspase recruitment domain family member 16 [Source:HGNC Symbol;Acc:HGNC:33701]"}, {"versioned_ensembl_gene_id":"ENSG00000248182.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29416825,"end":29417771,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000232569.8","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"GPRC3A,hGB1a","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555714,"end":29633284,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000128833.12","gene_symbol":"MYO5C","gene_name":"myosin VC [Source:HGNC Symbol;Acc:HGNC:7604]","synonyms":"MGC74969","biotype":"protein_coding","ncbi_id":"55930","summary":null,"start":52192322,"end":52295798,"strand":-1,"description":"myosin VC [Source:HGNC Symbol;Acc:HGNC:7604]"}, {"versioned_ensembl_gene_id":"ENSG00000226386.1","gene_symbol":"PARD3-AS1","gene_name":"PARD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44964]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505601","summary":null,"start":34815767,"end":34816386,"strand":1,"description":"PARD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44964]"}, {"versioned_ensembl_gene_id":"ENSG00000230193.3","gene_symbol":"MYL8P","gene_name":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]","synonyms":"BING3","biotype":"processed_pseudogene","ncbi_id":"442204","summary":null,"start":33267813,"end":33268330,"strand":1,"description":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]"}, {"versioned_ensembl_gene_id":"ENSG00000229494.1","gene_symbol":"AC012494.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78088730,"end":78127806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248733.1","gene_symbol":"AC008852.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58846885,"end":58863414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180383.3","gene_symbol":"DEFB124","gene_name":"defensin beta 124 [Source:HGNC Symbol;Acc:HGNC:18104]","synonyms":"DEFB-24","biotype":"protein_coding","ncbi_id":"245937","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the host immunologic response to invading microorganisms. This antimicrobial protein is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20q11.1. The encoded protein may serve to enhance innate immunity in the prostate. [provided by RefSeq, Nov 2014]","start":31465506,"end":31476757,"strand":-1,"description":"defensin beta 124 [Source:HGNC Symbol;Acc:HGNC:18104]"}, {"versioned_ensembl_gene_id":"ENSG00000262097.1","gene_symbol":"LINC02185","gene_name":"long intergenic non-protein coding RNA 2185 [Source:HGNC Symbol;Acc:HGNC:53047]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927311","summary":null,"start":14009280,"end":14016016,"strand":-1,"description":"long intergenic non-protein coding RNA 2185 [Source:HGNC Symbol;Acc:HGNC:53047]"}, {"versioned_ensembl_gene_id":"ENSG00000263234.1","gene_symbol":"AC010401.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13953155,"end":13954825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105479.15","gene_symbol":"CCDC114","gene_name":"coiled-coil domain containing 114 [Source:HGNC Symbol;Acc:HGNC:26560]","synonyms":"CILD20,FLJ32926","biotype":"protein_coding","ncbi_id":"93233","summary":"This gene encodes a coiled-coil domain-containing protein that is a component of the outer dynein arm docking complex in cilia cells. Mutations in this gene may cause primary ciliary dyskinesia 20. [provided by RefSeq, May 2013]","start":48296457,"end":48321894,"strand":-1,"description":"coiled-coil domain containing 114 [Source:HGNC Symbol;Acc:HGNC:26560]"}, {"versioned_ensembl_gene_id":"ENSG00000231205.11","gene_symbol":"ZNF826P","gene_name":"zinc finger protein 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:33875]","synonyms":"ZNF826,FLJ44894","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"664701","summary":null,"start":20340269,"end":20424969,"strand":-1,"description":"zinc finger protein 826, pseudogene [Source:HGNC Symbol;Acc:HGNC:33875]"}, {"versioned_ensembl_gene_id":"ENSG00000279331.1","gene_symbol":"RBM12B-AS1","gene_name":"RBM12B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28818]","synonyms":"PRO1905,C8orf39","biotype":"TEC","ncbi_id":"55472","summary":null,"start":93740121,"end":93740773,"strand":1,"description":"RBM12B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28818]"}, {"versioned_ensembl_gene_id":"ENSG00000254089.1","gene_symbol":"AC016885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93259667,"end":93297976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268174.1","gene_symbol":"BNIP3P22","gene_name":"BCL2 interacting protein 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:49702]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421706","summary":null,"start":20416514,"end":20417069,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:49702]"}, {"versioned_ensembl_gene_id":"ENSG00000268335.1","gene_symbol":"BNIP3P23","gene_name":"BCL2 interacting protein 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:49703]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421697","summary":null,"start":20443215,"end":20443725,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:49703]"}, {"versioned_ensembl_gene_id":"ENSG00000123815.11","gene_symbol":"COQ8B","gene_name":"coenzyme Q8B [Source:HGNC Symbol;Acc:HGNC:19041]","synonyms":"FLJ12229,COQ8,ADCK4","biotype":"protein_coding","ncbi_id":"79934","summary":"This gene encodes a protein with two copies of a domain found in protein kinases. The encoded protein has a complete protein kinase catalytic domain, and a truncated domain that contains only the active and binding sites of the protein kinase domain, however, it is not known whether the protein has any kinase activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":40691529,"end":40718207,"strand":-1,"description":"coenzyme Q8B [Source:HGNC Symbol;Acc:HGNC:19041]"}, {"versioned_ensembl_gene_id":"ENSG00000274488.4","gene_symbol":"LY6H","gene_name":"lymphocyte antigen 6 family member H [Source:HGNC Symbol;Acc:HGNC:6728]","synonyms":"NMLY6","biotype":"protein_coding","ncbi_id":"4062","summary":null,"start":143163211,"end":143166008,"strand":-1,"description":"lymphocyte antigen 6 family member H [Source:HGNC Symbol;Acc:HGNC:6728]"}, {"versioned_ensembl_gene_id":"ENSG00000086544.2","gene_symbol":"ITPKC","gene_name":"inositol-trisphosphate 3-kinase C [Source:HGNC Symbol;Acc:HGNC:14897]","synonyms":"IP3KC,IP3-3KC","biotype":"protein_coding","ncbi_id":"80271","summary":"This gene encodes a member of the inositol 1,4,5-trisphosphate [Ins(1,4,5)P(3)] 3-kinase family of enzymes that catalyze the phosphorylation of inositol 1,4,5-trisphosphate to 1,3,4,5-tetrakisphosphate. The encoded protein is localized to the nucleus and cytoplasm and has both nuclear import and nuclear export activity. Single nucleotide polymorphisms in this gene are associated with Kawasaki disease.[provided by RefSeq, Sep 2009]","start":40717103,"end":40740860,"strand":1,"description":"inositol-trisphosphate 3-kinase C [Source:HGNC Symbol;Acc:HGNC:14897]"}, {"versioned_ensembl_gene_id":"ENSG00000253536.1","gene_symbol":"AC138832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71475761,"end":71476316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270806.1","gene_symbol":"C17orf50","gene_name":"chromosome 17 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:29581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146853","summary":null,"start":35760897,"end":35765079,"strand":1,"description":"chromosome 17 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:29581]"}, {"versioned_ensembl_gene_id":"ENSG00000136881.11","gene_symbol":"BAAT","gene_name":"bile acid-CoA:amino acid N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:932]","synonyms":"BAT","biotype":"protein_coding","ncbi_id":"570","summary":"The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":101360417,"end":101383519,"strand":-1,"description":"bile acid-CoA:amino acid N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:932]"}, {"versioned_ensembl_gene_id":"ENSG00000255176.1","gene_symbol":"AP000941.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118636620,"end":118638097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063601.16","gene_symbol":"MTMR1","gene_name":"myotubularin related protein 1 [Source:HGNC Symbol;Acc:HGNC:7449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8776","summary":"This gene encodes a member of the myotubularin related family of proteins. Members of this family contain the consensus sequence for the active site of protein tyrosine phosphatases. Alternatively spliced variants have been described but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":150692971,"end":150765103,"strand":1,"description":"myotubularin related protein 1 [Source:HGNC Symbol;Acc:HGNC:7449]"}, {"versioned_ensembl_gene_id":"ENSG00000224114.1","gene_symbol":"AL591846.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206695837,"end":206696269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259645.1","gene_symbol":"AC027237.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":69391192,"end":69392149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280455.1","gene_symbol":"AL359745.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105690429,"end":105702689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268947.1","gene_symbol":"AC002128.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35262846,"end":35264804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143514.16","gene_symbol":"TP53BP2","gene_name":"tumor protein p53 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:12000]","synonyms":"ASPP2,53BP2,PPP1R13A","biotype":"protein_coding","ncbi_id":"7159","summary":"This gene encodes a member of the ASPP (apoptosis-stimulating protein of p53) family of p53 interacting proteins. The protein contains four ankyrin repeats and an SH3 domain involved in protein-protein interactions. It is localized to the perinuclear region of the cytoplasm, and regulates apoptosis and cell growth through interactions with other regulatory molecules including members of the p53 family. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":223779899,"end":223845972,"strand":-1,"description":"tumor protein p53 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:12000]"}, {"versioned_ensembl_gene_id":"ENSG00000244192.1","gene_symbol":"AC113367.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130989897,"end":130990428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249418.2","gene_symbol":"AC005741.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130598348,"end":130598779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168781.21","gene_symbol":"PPIP5K1","gene_name":"diphosphoinositol pentakisphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:29023]","synonyms":"VIP1,KIAA0377,IPS1,HISPPD2A","biotype":"protein_coding","ncbi_id":"9677","summary":"This gene encodes a dual functional inositol kinase. The encoded enzyme converts inositol hexakisphosphate to diphosphoinositol pentakisphosphate and diphosphoinositol pentakisphosphate to bis-diphosphoinositol tetrakisphosphate. This protein may be important for intracellular signaling pathways. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 15.[provided by RefSeq, Jun 2010]","start":43533462,"end":43590253,"strand":-1,"description":"diphosphoinositol pentakisphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:29023]"}, {"versioned_ensembl_gene_id":"ENSG00000166863.11","gene_symbol":"TAC3","gene_name":"tachykinin 3 [Source:HGNC Symbol;Acc:HGNC:11521]","synonyms":"ZNEUROK1,NKNB,NKB","biotype":"protein_coding","ncbi_id":"6866","summary":"This gene encodes a member of the tachykinin family of secreted neuropeptides. The encoded preproprotein is proteolytically processed to generate the mature peptide, which is primarily expressed in the central and peripheral nervous systems and functions as a neurotransmitter. This peptide is the ligand for the neurokinin-3 receptor. This protein is also expressed in the outer syncytiotrophoblast of the placenta and may be associated with pregnancy-induced hypertension and pre-eclampsia. Mutations in this gene are associated with normosmic hypogonadotropic hypogonadism. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":57010000,"end":57028883,"strand":-1,"description":"tachykinin 3 [Source:HGNC Symbol;Acc:HGNC:11521]"}, {"versioned_ensembl_gene_id":"ENSG00000231320.1","gene_symbol":"BX908738.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29229234,"end":29230164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148215.4","gene_symbol":"OR5C1","gene_name":"olfactory receptor family 5 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8331]","synonyms":"OR9-F,OR5C2P,hRPK-465_F_21","biotype":"protein_coding","ncbi_id":"392391","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122788933,"end":122789895,"strand":1,"description":"olfactory receptor family 5 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8331]"}, {"versioned_ensembl_gene_id":"ENSG00000249618.5","gene_symbol":"LINC02465","gene_name":"long intergenic non-protein coding RNA 2465 [Source:HGNC Symbol;Acc:HGNC:53403]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986313","summary":null,"start":129771659,"end":129955368,"strand":1,"description":"long intergenic non-protein coding RNA 2465 [Source:HGNC Symbol;Acc:HGNC:53403]"}, {"versioned_ensembl_gene_id":"ENSG00000249876.1","gene_symbol":"AC010285.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179939457,"end":179940132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174358.15","gene_symbol":"SLC6A19","gene_name":"solute carrier family 6 member 19 [Source:HGNC Symbol;Acc:HGNC:27960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340024","summary":"This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene may result in Hartnup disorder, an inherited disease with symptoms such as pellagra, cerebellar ataxia, and psychosis. The expression and function of B0AT1 (SLC6A19) in intestinal cells depends on the presence of the accessory protein angiotensin-converting enzyme 2 (ACE2) which, among other functions, acts as a chaperone for membrane trafficking of B0AT1. The ACE2 is also the cellular receptor for severe acute respiratory syndrome-coronavirus (SARS-CoV) and for SARS-CoV-2 that is causing the coronavirus 2019 (COVID-19) pandemic [provided by RefSeq, Jul 2020]","start":1201595,"end":1225117,"strand":1,"description":"solute carrier family 6 member 19 [Source:HGNC Symbol;Acc:HGNC:27960]"}, {"versioned_ensembl_gene_id":"ENSG00000229178.1","gene_symbol":"AC233280.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239617.1","gene_symbol":"AC073610.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48903418,"end":48903813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188985.6","gene_symbol":"DHFRP1","gene_name":"dihydrofolate reductase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"573971","summary":null,"start":26170726,"end":26171284,"strand":-1,"description":"dihydrofolate reductase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2862]"}, {"versioned_ensembl_gene_id":"ENSG00000269376.1","gene_symbol":"AL356740.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":113009671,"end":113010319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228914.2","gene_symbol":"OR1H1P","gene_name":"olfactory receptor family 1 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8206]","synonyms":"OST26,OR1H1","biotype":"unprocessed_pseudogene","ncbi_id":"26742","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122607864,"end":122608800,"strand":1,"description":"olfactory receptor family 1 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8206]"}, {"versioned_ensembl_gene_id":"ENSG00000171501.9","gene_symbol":"OR1N2","gene_name":"olfactory receptor family 1 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15111]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138882","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":122553112,"end":122554214,"strand":1,"description":"olfactory receptor family 1 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15111]"}, {"versioned_ensembl_gene_id":"ENSG00000160716.5","gene_symbol":"CHRNB2","gene_name":"cholinergic receptor nicotinic beta 2 subunit [Source:HGNC Symbol;Acc:HGNC:1962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1141","summary":"Neuronal acetylcholine receptors are homo- or heteropentameric complexes composed of homologous alpha and beta subunits. They belong to a superfamily of ligand-gated ion channels which allow the flow of sodium and potassium across the plasma membrane in response to ligands such as acetylcholine and nicotine. This gene encodes one of several beta subunits. Mutations in this gene are associated with autosomal dominant nocturnal frontal lobe epilepsy. [provided by RefSeq, Jul 2008]","start":154567781,"end":154580026,"strand":1,"description":"cholinergic receptor nicotinic beta 2 subunit [Source:HGNC Symbol;Acc:HGNC:1962]"}, {"versioned_ensembl_gene_id":"ENSG00000227470.1","gene_symbol":"AC073415.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108878308,"end":108878460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134285.10","gene_symbol":"FKBP11","gene_name":"FK506 binding protein 11 [Source:HGNC Symbol;Acc:HGNC:18624]","synonyms":"FKBP19","biotype":"protein_coding","ncbi_id":"51303","summary":"FKBP11 belongs to the FKBP family of peptidyl-prolyl cis/trans isomerases, which catalyze the folding of proline-containing polypeptides. The peptidyl-prolyl isomerase activity of FKBP proteins is inhibited by the immunosuppressant compounds FK506 and rapamycin (Rulten et al., 2006 [PubMed 16596453]).[supplied by OMIM, Mar 2008]","start":48921518,"end":48926474,"strand":-1,"description":"FK506 binding protein 11 [Source:HGNC Symbol;Acc:HGNC:18624]"}, {"versioned_ensembl_gene_id":"ENSG00000231465.2","gene_symbol":"AL359636.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122471358,"end":122475817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272140.2","gene_symbol":"AC022400.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73703735,"end":73713581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206127.10","gene_symbol":"GOLGA8O","gene_name":"golgin A8 family member O [Source:HGNC Symbol;Acc:HGNC:44406]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728047","summary":null,"start":32445106,"end":32455634,"strand":-1,"description":"golgin A8 family member O [Source:HGNC Symbol;Acc:HGNC:44406]"}, {"versioned_ensembl_gene_id":"ENSG00000250193.1","gene_symbol":"AC082650.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129299175,"end":129305022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271519.1","gene_symbol":"AL590065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35864858,"end":35869631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236508.1","gene_symbol":"ATP13A5-AS1","gene_name":"ATP13A5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41281]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874218","summary":null,"start":193307244,"end":193314362,"strand":1,"description":"ATP13A5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41281]"}, {"versioned_ensembl_gene_id":"ENSG00000171195.10","gene_symbol":"MUC7","gene_name":"mucin 7, secreted [Source:HGNC Symbol;Acc:HGNC:7518]","synonyms":"MG2,FLJ27047","biotype":"protein_coding","ncbi_id":"4589","summary":"This gene encodes a small salivary mucin, which is thought to play a role in facilitating the clearance of bacteria in the oral cavity and to aid in mastication, speech, and swallowing. The central domain of this glycoprotein contains tandem repeats, each composed of 23 amino acids. This antimicrobial protein has antibacterial and antifungal activity. The most common allele contains 6 repeats, and some alleles may be associated with susceptibility to asthma. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Oct 2014]","start":70430492,"end":70482997,"strand":1,"description":"mucin 7, secreted [Source:HGNC Symbol;Acc:HGNC:7518]"}, {"versioned_ensembl_gene_id":"ENSG00000225538.2","gene_symbol":"OR5BE1P","gene_name":"olfactory receptor family 5 subfamily BE member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15273]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81207","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56082801,"end":56084840,"strand":1,"description":"olfactory receptor family 5 subfamily BE member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15273]"}, {"versioned_ensembl_gene_id":"ENSG00000181780.4","gene_symbol":"OR5J1P","gene_name":"olfactory receptor family 5 subfamily J member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8348]","synonyms":"OR5J1,HTPCRH02","biotype":"unprocessed_pseudogene","ncbi_id":"401687","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56071111,"end":56072049,"strand":1,"description":"olfactory receptor family 5 subfamily J member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8348]"}, {"versioned_ensembl_gene_id":"ENSG00000236994.1","gene_symbol":"YBX1P9","gene_name":"Y-box binding protein 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42430]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861470","summary":null,"start":226318015,"end":226318693,"strand":-1,"description":"Y-box binding protein 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42430]"}, {"versioned_ensembl_gene_id":"ENSG00000178038.16","gene_symbol":"ALS2CL","gene_name":"ALS2 C-terminal like [Source:HGNC Symbol;Acc:HGNC:20605]","synonyms":"RN49018,FLJ36525,DKFZp686I0110","biotype":"protein_coding","ncbi_id":"259173","summary":null,"start":46668997,"end":46693704,"strand":-1,"description":"ALS2 C-terminal like [Source:HGNC Symbol;Acc:HGNC:20605]"}, {"versioned_ensembl_gene_id":"ENSG00000219532.2","gene_symbol":"AL139805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131819803,"end":131820091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125378.15","gene_symbol":"BMP4","gene_name":"bone morphogenetic protein 4 [Source:HGNC Symbol;Acc:HGNC:1071]","synonyms":"BMP2B","biotype":"protein_coding","ncbi_id":"652","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates heart development and adipogenesis. Mutations in this gene are associated with orofacial cleft and microphthalmia in human patients. The encoded protein may also be involved in the pathology of multiple cardiovascular diseases and human cancers. [provided by RefSeq, Jul 2016]","start":53949736,"end":53958761,"strand":-1,"description":"bone morphogenetic protein 4 [Source:HGNC Symbol;Acc:HGNC:1071]"}, {"versioned_ensembl_gene_id":"ENSG00000066697.14","gene_symbol":"MSANTD3","gene_name":"Myb/SANT DNA binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23370]","synonyms":"MGC17337,C9orf30","biotype":"protein_coding","ncbi_id":"91283","summary":null,"start":100427156,"end":100451711,"strand":1,"description":"Myb/SANT DNA binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23370]"}, {"versioned_ensembl_gene_id":"ENSG00000225691.7","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31345885,"end":31349256,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000233947.1","gene_symbol":"AL353705.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78178263,"end":78179512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137171.14","gene_symbol":"KLC4","gene_name":"kinesin light chain 4 [Source:HGNC Symbol;Acc:HGNC:21624]","synonyms":"KNSL8,bA387M24.3","biotype":"protein_coding","ncbi_id":"89953","summary":null,"start":43040777,"end":43075099,"strand":1,"description":"kinesin light chain 4 [Source:HGNC Symbol;Acc:HGNC:21624]"}, {"versioned_ensembl_gene_id":"ENSG00000234242.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BPG309N1.15,BAT1P2","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29982716,"end":29983112,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000267125.2","gene_symbol":"AC012615.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1852382,"end":1853622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105808.17","gene_symbol":"RASA4","gene_name":"RAS p21 protein activator 4 [Source:HGNC Symbol;Acc:HGNC:23181]","synonyms":"KIAA0538,GAPL,CAPRI","biotype":"protein_coding","ncbi_id":"10156","summary":"This gene encodes a member of the GAP1 family of GTPase-activating proteins that suppresses the Ras/mitogen-activated protein kinase pathway in response to Ca(2+). Stimuli that increase intracellular Ca(2+) levels result in the translocation of this protein to the plasma membrane, where it activates Ras GTPase activity. Consequently, Ras is converted from the active GTP-bound state to the inactive GDP-bound state and no longer activates downstream pathways that regulate gene expression, cell growth, and differentiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":102573807,"end":102616757,"strand":-1,"description":"RAS p21 protein activator 4 [Source:HGNC Symbol;Acc:HGNC:23181]"}, {"versioned_ensembl_gene_id":"ENSG00000095627.9","gene_symbol":"TDRD1","gene_name":"tudor domain containing 1 [Source:HGNC Symbol;Acc:HGNC:11712]","synonyms":"CT41.1","biotype":"protein_coding","ncbi_id":"56165","summary":"This gene encodes a protein containing a tudor domain that is thought to function in the suppression of transposable elements during spermatogenesis. The related protein in mouse forms a complex with piRNAs and Piwi proteins to promote methylation and silencing of target sequences. This gene was observed to be upregulated by ETS transcription factor ERG in prostate tumors. [provided by RefSeq, Sep 2018]","start":114179270,"end":114232304,"strand":1,"description":"tudor domain containing 1 [Source:HGNC Symbol;Acc:HGNC:11712]"}, {"versioned_ensembl_gene_id":"ENSG00000255241.1","gene_symbol":"AP005436.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88098591,"end":88115835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167676.4","gene_symbol":"PLIN4","gene_name":"perilipin 4 [Source:HGNC Symbol;Acc:HGNC:29393]","synonyms":"S3-12,KIAA1881","biotype":"protein_coding","ncbi_id":"729359","summary":"Members of the perilipin family, such as PLIN4, coat intracellular lipid storage droplets (Wolins et al., 2003 [PubMed 12840023]).[supplied by OMIM, Feb 2010]","start":4502180,"end":4518465,"strand":-1,"description":"perilipin 4 [Source:HGNC Symbol;Acc:HGNC:29393]"}, {"versioned_ensembl_gene_id":"ENSG00000274434.1","gene_symbol":"AC142525.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69593256,"end":69594998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128000.15","gene_symbol":"ZNF780B","gene_name":"zinc finger protein 780B [Source:HGNC Symbol;Acc:HGNC:33109]","synonyms":"ZNF779","biotype":"protein_coding","ncbi_id":"163131","summary":null,"start":40028260,"end":40056209,"strand":-1,"description":"zinc finger protein 780B [Source:HGNC Symbol;Acc:HGNC:33109]"}, {"versioned_ensembl_gene_id":"ENSG00000281167.1","gene_symbol":"AL355390.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74434538,"end":74555515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226240.1","gene_symbol":"LINC00381","gene_name":"long intergenic non-protein coding RNA 381 [Source:HGNC Symbol;Acc:HGNC:42708]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874151","summary":null,"start":74419173,"end":74435159,"strand":1,"description":"long intergenic non-protein coding RNA 381 [Source:HGNC Symbol;Acc:HGNC:42708]"}, {"versioned_ensembl_gene_id":"ENSG00000258483.2","gene_symbol":"LINC02251","gene_name":"long intergenic non-protein coding RNA 2251 [Source:HGNC Symbol;Acc:HGNC:53149]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371008","summary":null,"start":98003081,"end":98021777,"strand":1,"description":"long intergenic non-protein coding RNA 2251 [Source:HGNC Symbol;Acc:HGNC:53149]"}, {"versioned_ensembl_gene_id":"ENSG00000205767.4","gene_symbol":"AL136038.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63567958,"end":63568308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261242.1","gene_symbol":"AL136038.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63543569,"end":63544664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283020.1","gene_symbol":"ABBA01031674.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878636,"end":29879363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261766.1","gene_symbol":"AC133550.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28862166,"end":28863340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258422.5","gene_symbol":"AL160191.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70187123,"end":70230187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236580.1","gene_symbol":"AC073626.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114297114,"end":114297429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109819.8","gene_symbol":"PPARGC1A","gene_name":"PPARG coactivator 1 alpha [Source:HGNC Symbol;Acc:HGNC:9237]","synonyms":"PPARGC1,PGC1A,PGC1,PGC-1alpha","biotype":"protein_coding","ncbi_id":"10891","summary":"The protein encoded by this gene is a transcriptional coactivator that regulates the genes involved in energy metabolism. This protein interacts with PPARgamma, which permits the interaction of this protein with multiple transcription factors. This protein can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination. This protein may be also involved in controlling blood pressure, regulating cellular cholesterol homoeostasis, and the development of obesity. [provided by RefSeq, Jul 2008]","start":23755041,"end":23904089,"strand":-1,"description":"PPARG coactivator 1 alpha [Source:HGNC Symbol;Acc:HGNC:9237]"}, {"versioned_ensembl_gene_id":"ENSG00000228844.1","gene_symbol":"AL358176.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240636599,"end":240637052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260954.1","gene_symbol":"AL133297.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1579242,"end":1580308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264212.1","gene_symbol":"AC103808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76256891,"end":76258337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231440.1","gene_symbol":"AL358176.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":240588522,"end":240590748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276785.4","gene_symbol":"PRSS58","gene_name":"protease, serine 58 [Source:HGNC Symbol;Acc:HGNC:39125]","synonyms":"TRYX3","biotype":"protein_coding","ncbi_id":"136541","summary":"This gene encodes a member of the trypsin family of serine proteases. This gene and several related trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. This gene was previously described as a trypsinogen-like pseudogene, but it is now thought to be a protein-coding gene. [provided by RefSeq, Jul 2008]","start":142252163,"end":142258078,"strand":-1,"description":"protease, serine 58 [Source:HGNC Symbol;Acc:HGNC:39125]"}, {"versioned_ensembl_gene_id":"ENSG00000234404.2","gene_symbol":"SPRYD7P1","gene_name":"SPRY domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130843","summary":null,"start":77374212,"end":77381319,"strand":1,"description":"SPRY domain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52300]"}, {"versioned_ensembl_gene_id":"ENSG00000230807.1","gene_symbol":"AC099535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27486247,"end":27486617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266014.1","gene_symbol":"AC103808.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76247725,"end":76251388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198774.4","gene_symbol":"RASSF9","gene_name":"Ras association domain family member 9 [Source:HGNC Symbol;Acc:HGNC:15739]","synonyms":"PAMCI,P-CIP1","biotype":"protein_coding","ncbi_id":"9182","summary":"The protein encoded by this gene localizes to perinuclear endosomes. This protein associates with peptidylglycine alpha-amidating monooxygenase, and may be involved with the trafficking of this enzyme through secretory or endosomal pathways. [provided by RefSeq, Jul 2008]","start":85800697,"end":85836570,"strand":-1,"description":"Ras association domain family member 9 [Source:HGNC Symbol;Acc:HGNC:15739]"}, {"versioned_ensembl_gene_id":"ENSG00000258874.1","gene_symbol":"AC009396.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78703615,"end":78709934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280348.1","gene_symbol":"AL138713.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73800074,"end":73802203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154781.15","gene_symbol":"CCDC174","gene_name":"coiled-coil domain containing 174 [Source:HGNC Symbol;Acc:HGNC:28033]","synonyms":"FLJ33839,C3orf19","biotype":"protein_coding","ncbi_id":"51244","summary":"The protein encoded by this gene is found in the nucleus, where it interacts with eukaryotic translation initiation factor 4A, isoform 3. The encoded protein appears to be a part of the exon junction complex, which is involved in RNA processing, translation, and nonsense-mediated mRNA decay. A mutation in this gene has been associated with infantile hypotonia with psychomotor retardation. [provided by RefSeq, Mar 2016]","start":14651746,"end":14672659,"strand":1,"description":"coiled-coil domain containing 174 [Source:HGNC Symbol;Acc:HGNC:28033]"}, {"versioned_ensembl_gene_id":"ENSG00000232684.1","gene_symbol":"ATP11A-AS1","gene_name":"ATP11A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40645]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874205","summary":null,"start":112745449,"end":112754693,"strand":-1,"description":"ATP11A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40645]"}, {"versioned_ensembl_gene_id":"ENSG00000146021.14","gene_symbol":"KLHL3","gene_name":"kelch like family member 3 [Source:HGNC Symbol;Acc:HGNC:6354]","synonyms":"KIAA1129","biotype":"protein_coding","ncbi_id":"26249","summary":"This gene is ubiquitously expressed and encodes a full-length protein which has an N-terminal BTB domain followed by a BACK domain and six kelch-like repeats in the C-terminus. These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex. Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D); a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2012]","start":137617500,"end":137736090,"strand":-1,"description":"kelch like family member 3 [Source:HGNC Symbol;Acc:HGNC:6354]"}, {"versioned_ensembl_gene_id":"ENSG00000070601.9","gene_symbol":"FRMPD1","gene_name":"FERM and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29159]","synonyms":"KIAA0967,FRMD2","biotype":"protein_coding","ncbi_id":"22844","summary":null,"start":37651000,"end":37746904,"strand":1,"description":"FERM and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29159]"}, {"versioned_ensembl_gene_id":"ENSG00000256928.1","gene_symbol":"AP000763.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73395559,"end":73396436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212747.4","gene_symbol":"RTL8B","gene_name":"retrotransposon Gag like 8B [Source:HGNC Symbol;Acc:HGNC:33156]","synonyms":"SIRH4,MAR8B,FAM127C,CXX1c","biotype":"protein_coding","ncbi_id":"441518","summary":null,"start":135020504,"end":135022529,"strand":-1,"description":"retrotransposon Gag like 8B [Source:HGNC Symbol;Acc:HGNC:33156]"}, {"versioned_ensembl_gene_id":"ENSG00000180318.3","gene_symbol":"ALX1","gene_name":"ALX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:1494]","synonyms":"CART1","biotype":"protein_coding","ncbi_id":"8092","summary":"The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]","start":85280107,"end":85301784,"strand":1,"description":"ALX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:1494]"}, {"versioned_ensembl_gene_id":"ENSG00000224116.6","gene_symbol":"INHBA-AS1","gene_name":"INHBA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40303]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285954","summary":null,"start":41693916,"end":41779388,"strand":1,"description":"INHBA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40303]"}, {"versioned_ensembl_gene_id":"ENSG00000256870.2","gene_symbol":"SLC5A8","gene_name":"solute carrier family 5 member 8 [Source:HGNC Symbol;Acc:HGNC:19119]","synonyms":"AIT","biotype":"protein_coding","ncbi_id":"160728","summary":"SLC5A8 has been shown to transport iodide by a passive mechanism (Rodriguez et al., 2002 [PubMed 12107270]) and monocarboxylates and short-chain fatty acids by a sodium-coupled mechanism (Gopal et al., 2004 [PubMed 15322102]). In kidney, SLC5A8 functions as a high-affinity sodium-coupled lactate transporter involved in reabsorption of lactate and maintenance of blood lactate levels (Thangaraju et al., 2006 [PubMed 16873376]).[supplied by OMIM, Dec 2008]","start":101155493,"end":101210407,"strand":-1,"description":"solute carrier family 5 member 8 [Source:HGNC Symbol;Acc:HGNC:19119]"}, {"versioned_ensembl_gene_id":"ENSG00000255499.1","gene_symbol":"AC036111.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55865709,"end":55865820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237802.6","gene_symbol":"FAM197Y6","gene_name":"family with sequence similarity 197 Y-linked member 6 [Source:HGNC Symbol;Acc:HGNC:37468]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"105379270","summary":null,"start":9388122,"end":9397438,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 6 [Source:HGNC Symbol;Acc:HGNC:37468]"}, {"versioned_ensembl_gene_id":"ENSG00000269916.1","gene_symbol":"AC133794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85263544,"end":85264457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102317.17","gene_symbol":"RBM3","gene_name":"RNA binding motif (RNP1, RRM) protein 3 [Source:HGNC Symbol;Acc:HGNC:9900]","synonyms":"IS1-RNPL","biotype":"protein_coding","ncbi_id":"5935","summary":"This gene is a member of the glycine-rich RNA-binding protein family and encodes a protein with one RNA recognition motif (RRM) domain. Expression of this gene is induced by cold shock and low oxygen tension. A pseudogene exists on chromosome 1. Multiple alternatively spliced transcript variants that are predicted to encode different isoforms have been characterized although some of these variants fit nonsense-mediated decay (NMD) criteria. [provided by RefSeq, Jul 2008]","start":48574449,"end":48579066,"strand":1,"description":"RNA binding motif (RNP1, RRM) protein 3 [Source:HGNC Symbol;Acc:HGNC:9900]"}, {"versioned_ensembl_gene_id":"ENSG00000173826.14","gene_symbol":"KCNH6","gene_name":"potassium voltage-gated channel subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:18862]","synonyms":"Kv11.2,HERG2,erg2","biotype":"protein_coding","ncbi_id":"81033","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":63523334,"end":63548977,"strand":1,"description":"potassium voltage-gated channel subfamily H member 6 [Source:HGNC Symbol;Acc:HGNC:18862]"}, {"versioned_ensembl_gene_id":"ENSG00000126952.16","gene_symbol":"NXF5","gene_name":"nuclear RNA export factor 5 [Source:HGNC Symbol;Acc:HGNC:8075]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55998","summary":"This gene is one member of a family of nuclear RNA export factor genes. The encoded protein can bind RNA, and is implicated in mRNA nuclear export. However, this protein has lost several C-terminal protein domains found in other family members that are required for export activity, and may be an evolving pseudogene. Alternatively spliced transcript variants have been described, but most are candidates for nonsense-mediated decay (NMD) and may not express proteins in vivo. [provided by RefSeq, Jul 2009]","start":101832112,"end":101857577,"strand":-1,"description":"nuclear RNA export factor 5 [Source:HGNC Symbol;Acc:HGNC:8075]"}, {"versioned_ensembl_gene_id":"ENSG00000107371.12","gene_symbol":"EXOSC3","gene_name":"exosome component 3 [Source:HGNC Symbol;Acc:HGNC:17944]","synonyms":"Rrp40p,RRP40,p10,hRrp40p,hRrp-40,CGI-102","biotype":"protein_coding","ncbi_id":"51010","summary":"This gene encodes a non-catalytic component of the human exosome, a complex with 3'-5' exoribonuclease activity that plays a role in numerous RNA processing and degradation activities. Related pseudogenes of this gene are found on chromosome 19 and 21. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2012]","start":37766978,"end":37801437,"strand":-1,"description":"exosome component 3 [Source:HGNC Symbol;Acc:HGNC:17944]"}, {"versioned_ensembl_gene_id":"ENSG00000224353.2","gene_symbol":"ACE3P","gene_name":"angiotensin I converting enzyme 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44365]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100129123","summary":null,"start":63507056,"end":63519806,"strand":1,"description":"angiotensin I converting enzyme 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44365]"}, {"versioned_ensembl_gene_id":"ENSG00000188439.3","gene_symbol":"OR4P1P","gene_name":"olfactory receptor family 4 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14754]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79308","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55683239,"end":55684374,"strand":1,"description":"olfactory receptor family 4 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14754]"}, {"versioned_ensembl_gene_id":"ENSG00000268318.5","gene_symbol":"LINC01872","gene_name":"long intergenic non-protein coding RNA 1872 [Source:HGNC Symbol;Acc:HGNC:52691]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372444","summary":null,"start":51271266,"end":51281234,"strand":1,"description":"long intergenic non-protein coding RNA 1872 [Source:HGNC Symbol;Acc:HGNC:52691]"}, {"versioned_ensembl_gene_id":"ENSG00000184163.3","gene_symbol":"C1QTNF12","gene_name":"C1q and TNF related 12 [Source:HGNC Symbol;Acc:HGNC:32308]","synonyms":"C1QDC2,ADIPOLIN,MGC105127,FAM132A,CTRP12","biotype":"protein_coding","ncbi_id":"388581","summary":null,"start":1242446,"end":1246722,"strand":-1,"description":"C1q and TNF related 12 [Source:HGNC Symbol;Acc:HGNC:32308]"}, {"versioned_ensembl_gene_id":"ENSG00000203697.11","gene_symbol":"CAPN8","gene_name":"calpain 8 [Source:HGNC Symbol;Acc:HGNC:1485]","synonyms":"nCL-2","biotype":"protein_coding","ncbi_id":"388743","summary":null,"start":223538007,"end":223665734,"strand":-1,"description":"calpain 8 [Source:HGNC Symbol;Acc:HGNC:1485]"}, {"versioned_ensembl_gene_id":"ENSG00000100652.4","gene_symbol":"SLC10A1","gene_name":"solute carrier family 10 member 1 [Source:HGNC Symbol;Acc:HGNC:10905]","synonyms":"NTCP","biotype":"protein_coding","ncbi_id":"6554","summary":"The protein encoded by this gene belongs to the sodium/bile acid cotransporter family, which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids. Two homologous transporters are involved in the reabsorption of bile acids; the ileal sodium/bile acid cotransporter with an apical cell localization that absorbs bile acids from the intestinal lumen, bile duct and kidney, and the liver-specific sodium/bile acid cotransporter, represented by this protein, that is found in the basolateral membranes of hepatocytes. Bile acids are the catabolic product of cholesterol metabolism, hence this protein is important for cholesterol homeostasis. [provided by RefSeq, Oct 2011]","start":69775417,"end":69797289,"strand":-1,"description":"solute carrier family 10 member 1 [Source:HGNC Symbol;Acc:HGNC:10905]"}, {"versioned_ensembl_gene_id":"ENSG00000279858.1","gene_symbol":"AC068880.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19375128,"end":19375622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279265.1","gene_symbol":"AC000123.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127349833,"end":127350293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224138.1","gene_symbol":"AC000123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127350128,"end":127351523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233301.1","gene_symbol":"OR4C14P","gene_name":"olfactory receptor family 4 subfamily C member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:15170]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81310","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55537002,"end":55537924,"strand":1,"description":"olfactory receptor family 4 subfamily C member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:15170]"}, {"versioned_ensembl_gene_id":"ENSG00000234805.1","gene_symbol":"AC090505.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":194755589,"end":194757422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196395.7","gene_symbol":"AC244505.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52824269,"end":52829267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226083.5","gene_symbol":"SLC39A12-AS1","gene_name":"SLC39A12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44881]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129213","summary":null,"start":18001786,"end":18010562,"strand":-1,"description":"SLC39A12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44881]"}, {"versioned_ensembl_gene_id":"ENSG00000253143.3","gene_symbol":"AC022730.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70471112,"end":70480623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253967.1","gene_symbol":"AC022730.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70471134,"end":70485687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230834.1","gene_symbol":"AC068580.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1776930,"end":1778388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166855.9","gene_symbol":"CLPX","gene_name":"caseinolytic mitochondrial matrix peptidase chaperone subunit [Source:HGNC Symbol;Acc:HGNC:2088]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10845","summary":"The protein encoded by this gene is part of a protease found in mitochondria. This protease is ATP-dependent and targets specific proteins for degradation. The protease consists of two heptameric rings of the CLPP catalytic subunit sandwiched between two hexameric rings of the chaperone subunit encoded by this gene. Targeted proteins are unwound by this protein and then passed on to the CLPP subunit for degradation. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Nov 2015]","start":65148219,"end":65185342,"strand":-1,"description":"caseinolytic mitochondrial matrix peptidase chaperone subunit [Source:HGNC Symbol;Acc:HGNC:2088]"}, {"versioned_ensembl_gene_id":"ENSG00000250284.1","gene_symbol":"AC109439.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136734927,"end":136754686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254899.1","gene_symbol":"BX248516.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31520968,"end":31537331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261667.1","gene_symbol":"LY6L","gene_name":"lymphocyte antigen 6 family member L [Source:HGNC Symbol;Acc:HGNC:52284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928108","summary":null,"start":143080457,"end":143083001,"strand":1,"description":"lymphocyte antigen 6 family member L [Source:HGNC Symbol;Acc:HGNC:52284]"}, {"versioned_ensembl_gene_id":"ENSG00000256422.5","gene_symbol":"LINC02552","gene_name":"long intergenic non-protein coding RNA 2552 [Source:HGNC Symbol;Acc:HGNC:53587]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723895","summary":null,"start":104445868,"end":104609321,"strand":-1,"description":"long intergenic non-protein coding RNA 2552 [Source:HGNC Symbol;Acc:HGNC:53587]"}, {"versioned_ensembl_gene_id":"ENSG00000243328.1","gene_symbol":"AC083982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143065915,"end":143066587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237350.1","gene_symbol":"CDC42P6","gene_name":"cell division cycle 42 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44430]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643751","summary":null,"start":22727375,"end":22727950,"strand":-1,"description":"cell division cycle 42 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44430]"}, {"versioned_ensembl_gene_id":"ENSG00000259201.1","gene_symbol":"AC090971.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51887560,"end":51901123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259398.1","gene_symbol":"AC090970.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52033707,"end":52035625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174243.9","gene_symbol":"DDX23","gene_name":"DEAD-box helicase 23 [Source:HGNC Symbol;Acc:HGNC:17347]","synonyms":"U5-100K,SNRNP100,PRPF28,prp28","biotype":"protein_coding","ncbi_id":"9416","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a component of the U5 snRNP complex; it may facilitate conformational changes in the spliceosome during nuclear pre-mRNA splicing. An alternatively spliced transcript variant has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":48829764,"end":48852842,"strand":-1,"description":"DEAD-box helicase 23 [Source:HGNC Symbol;Acc:HGNC:17347]"}, {"versioned_ensembl_gene_id":"ENSG00000229328.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044223,"end":29045250,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000254987.1","gene_symbol":"AP002989.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103675994,"end":103895271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282827.2","gene_symbol":"AC134772.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":48446846,"end":48467645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169876.13","gene_symbol":"MUC17","gene_name":"mucin 17, cell surface associated [Source:HGNC Symbol;Acc:HGNC:16800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140453","summary":"The protein encoded by this gene is a membrane-bound mucin that provides protection to gut epithelial cells. The encoded protein contains about 60 tandem repeats, with each repeat being around 60 aa. N-glycosylation enables the encoded protein to localize on the cell surface, while the C-terminus interacts with the scaffold protein PDZ domain containing 1 (PDZK1). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Nov 2015]","start":101020072,"end":101058745,"strand":1,"description":"mucin 17, cell surface associated [Source:HGNC Symbol;Acc:HGNC:16800]"}, {"versioned_ensembl_gene_id":"ENSG00000186675.6","gene_symbol":"MAGEE2","gene_name":"MAGE family member E2 [Source:HGNC Symbol;Acc:HGNC:24935]","synonyms":"HCA3","biotype":"protein_coding","ncbi_id":"139599","summary":"This gene encodes a member of the E subfamily of MAGE (melanoma antigen-encoding gene) gene family. The gene is intronless and the encoded protein has two of the MAGE domains which are characteristic of MAGE family proteins. [provided by RefSeq, Sep 2011]","start":75782988,"end":75785236,"strand":-1,"description":"MAGE family member E2 [Source:HGNC Symbol;Acc:HGNC:24935]"}, {"versioned_ensembl_gene_id":"ENSG00000232717.1","gene_symbol":"TRIM51JP","gene_name":"tripartite motif-containing 51J, pseudogene [Source:HGNC Symbol;Acc:HGNC:43978]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643126","summary":null,"start":95574899,"end":95580764,"strand":1,"description":"tripartite motif-containing 51J, pseudogene [Source:HGNC Symbol;Acc:HGNC:43978]"}, {"versioned_ensembl_gene_id":"ENSG00000273476.1","gene_symbol":"AL133215.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100967688,"end":100968135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283473.2","gene_symbol":"FAM240A","gene_name":"family with sequence similarity 240 member A [Source:HGNC Symbol;Acc:HGNC:52390]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132146","summary":null,"start":46612435,"end":46626543,"strand":1,"description":"family with sequence similarity 240 member A [Source:HGNC Symbol;Acc:HGNC:52390]"}, {"versioned_ensembl_gene_id":"ENSG00000283877.1","gene_symbol":"AC104304.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46581150,"end":46617226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172869.14","gene_symbol":"DMXL1","gene_name":"Dmx like 1 [Source:HGNC Symbol;Acc:HGNC:2937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1657","summary":"The protein encoded by this gene is a member of the WD repeat superfamily of proteins, which have regulatory functions. This gene is expressed in many tissue types including several types of eye tissue, and it has been associated with ocular phenotypes. In addition, it is upregulated in cultured cells that overexpress growth factor independence 1B, a transcription factor that is essential for hematopoietic cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":119037772,"end":119249138,"strand":1,"description":"Dmx like 1 [Source:HGNC Symbol;Acc:HGNC:2937]"}, {"versioned_ensembl_gene_id":"ENSG00000260271.1","gene_symbol":"AL132996.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90345219,"end":90362632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181950.3","gene_symbol":"OR4A13P","gene_name":"olfactory receptor family 4 subfamily A member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15150]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81330","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55466771,"end":55467712,"strand":1,"description":"olfactory receptor family 4 subfamily A member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:15150]"}, {"versioned_ensembl_gene_id":"ENSG00000280011.1","gene_symbol":"AL031595.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44210442,"end":44229512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115364.13","gene_symbol":"MRPL19","gene_name":"mitochondrial ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:14052]","synonyms":"RPML15,RLX1,MRP-L15,KIAA0104","biotype":"protein_coding","ncbi_id":"9801","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":75646783,"end":75690851,"strand":1,"description":"mitochondrial ribosomal protein L19 [Source:HGNC Symbol;Acc:HGNC:14052]"}, {"versioned_ensembl_gene_id":"ENSG00000171101.13","gene_symbol":"SIGLEC17P","gene_name":"sialic acid binding Ig like lectin 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:15604]","synonyms":"SIGLECP3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284367","summary":null,"start":51167328,"end":51173524,"strand":1,"description":"sialic acid binding Ig like lectin 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:15604]"}, {"versioned_ensembl_gene_id":"ENSG00000151572.16","gene_symbol":"ANO4","gene_name":"anoctamin 4 [Source:HGNC Symbol;Acc:HGNC:23837]","synonyms":"FLJ34221,TMEM16D,FLJ35277,FLJ34272","biotype":"protein_coding","ncbi_id":"121601","summary":null,"start":100717526,"end":101128641,"strand":1,"description":"anoctamin 4 [Source:HGNC Symbol;Acc:HGNC:23837]"}, {"versioned_ensembl_gene_id":"ENSG00000258007.1","gene_symbol":"AC063947.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101038420,"end":101039094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277363.4","gene_symbol":"SRCIN1","gene_name":"SRC kinase signaling inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:29506]","synonyms":"SNIP,p140Cap,KIAA1684","biotype":"protein_coding","ncbi_id":"80725","summary":null,"start":38530016,"end":38605930,"strand":-1,"description":"SRC kinase signaling inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:29506]"}, {"versioned_ensembl_gene_id":"ENSG00000274996.1","gene_symbol":"AC006449.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38601049,"end":38602701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174177.12","gene_symbol":"CTU2","gene_name":"cytosolic thiouridylase subunit 2 [Source:HGNC Symbol;Acc:HGNC:28005]","synonyms":"NCS2,C16orf84","biotype":"protein_coding","ncbi_id":"348180","summary":"This gene encodes a protein which is involved in the post-transcriptional modification of transfer RNAs (tRNAs). The encoded protein plays a role in thiolation of uridine residue present at the wobble position in a subset of tRNAs, resulting in enhanced codon reading accuracy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":88706463,"end":88715386,"strand":1,"description":"cytosolic thiouridylase subunit 2 [Source:HGNC Symbol;Acc:HGNC:28005]"}, {"versioned_ensembl_gene_id":"ENSG00000260351.1","gene_symbol":"AC024270.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83022571,"end":83090782,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265437.1","gene_symbol":"AP005212.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14361434,"end":14361943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233693.1","gene_symbol":"AL357568.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":164769116,"end":164774641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204301.6","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32194843,"end":32224067,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000251239.1","gene_symbol":"AC004590.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50627032,"end":50631940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109171.14","gene_symbol":"SLAIN2","gene_name":"SLAIN motif family member 2 [Source:HGNC Symbol;Acc:HGNC:29282]","synonyms":"KIAA1458,FLJ21611","biotype":"protein_coding","ncbi_id":"57606","summary":null,"start":48341322,"end":48426212,"strand":1,"description":"SLAIN motif family member 2 [Source:HGNC Symbol;Acc:HGNC:29282]"}, {"versioned_ensembl_gene_id":"ENSG00000147596.3","gene_symbol":"PRDM14","gene_name":"PR/SET domain 14 [Source:HGNC Symbol;Acc:HGNC:14001]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63978","summary":"This gene encodes a member of the PRDI-BF1 and RIZ homology domain containing (PRDM) family of transcriptional regulators. The encoded protein may possess histone methyltransferase activity and plays a critical role in cell pluripotency by suppressing the expression of differentiation marker genes. Expression of this gene may play a role in breast cancer. [provided by RefSeq, Dec 2011]","start":70051651,"end":70071693,"strand":-1,"description":"PR/SET domain 14 [Source:HGNC Symbol;Acc:HGNC:14001]"}, {"versioned_ensembl_gene_id":"ENSG00000282165.1","gene_symbol":"AC243621.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45919274,"end":45922376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165474.5","gene_symbol":"GJB2","gene_name":"gap junction protein beta 2 [Source:HGNC Symbol;Acc:HGNC:4284]","synonyms":"DFNB1,DFNA3,CX26,NSRD1","biotype":"protein_coding","ncbi_id":"2706","summary":"This gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells. The gap junction proteins, also known as connexins, purified from fractions of enriched gap junctions from different tissues differ. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene are responsible for as much as 50% of pre-lingual, recessive deafness. [provided by RefSeq, Oct 2008]","start":20187470,"end":20192898,"strand":-1,"description":"gap junction protein beta 2 [Source:HGNC Symbol;Acc:HGNC:4284]"}, {"versioned_ensembl_gene_id":"ENSG00000196085.5","gene_symbol":"AC013442.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35219377,"end":35219604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156009.9","gene_symbol":"MAGEA8","gene_name":"MAGE family member A8 [Source:HGNC Symbol;Acc:HGNC:6806]","synonyms":"MGC2182,MAGE8,CT1.8","biotype":"protein_coding","ncbi_id":"4107","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2009]","start":149881141,"end":149885835,"strand":1,"description":"MAGE family member A8 [Source:HGNC Symbol;Acc:HGNC:6806]"}, {"versioned_ensembl_gene_id":"ENSG00000270307.1","gene_symbol":"MTATP6P2","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44576]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287745","summary":null,"start":100051920,"end":100052597,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44576]"}, {"versioned_ensembl_gene_id":"ENSG00000277747.1","gene_symbol":"AC133104.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95460144,"end":95460336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204705.3","gene_symbol":"UBTFL5","gene_name":"upstream binding transcription factor, RNA polymerase I-like 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35405]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728231","summary":null,"start":95450310,"end":95451500,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:35405]"}, {"versioned_ensembl_gene_id":"ENSG00000270350.1","gene_symbol":"MTND4LP5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075235","summary":null,"start":100050359,"end":100050650,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42239]"}, {"versioned_ensembl_gene_id":"ENSG00000270906.1","gene_symbol":"MTND4P35","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:51949]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075117","summary":null,"start":100048988,"end":100050362,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:51949]"}, {"versioned_ensembl_gene_id":"ENSG00000240271.1","gene_symbol":"AC090142.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105011107,"end":105011568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254141.1","gene_symbol":"AC103853.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":105669991,"end":105679031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165806.19","gene_symbol":"CASP7","gene_name":"caspase 7 [Source:HGNC Symbol;Acc:HGNC:1508]","synonyms":"MCH3,ICE-LAP3,CMH-1","biotype":"protein_coding","ncbi_id":"840","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. The precursor of the encoded protein is cleaved by caspase 3 and 10, is activated upon cell death stimuli and induces apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":113679162,"end":113730907,"strand":1,"description":"caspase 7 [Source:HGNC Symbol;Acc:HGNC:1508]"}, {"versioned_ensembl_gene_id":"ENSG00000140280.13","gene_symbol":"LYSMD2","gene_name":"LysM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28571]","synonyms":"MGC35274","biotype":"protein_coding","ncbi_id":"256586","summary":null,"start":51723011,"end":51751585,"strand":-1,"description":"LysM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28571]"}, {"versioned_ensembl_gene_id":"ENSG00000275005.1","gene_symbol":"AL354950.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129845328,"end":129845895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108001.13","gene_symbol":"EBF3","gene_name":"early B-cell factor 3 [Source:HGNC Symbol;Acc:HGNC:19087]","synonyms":"DKFZp667B0210,COE3","biotype":"protein_coding","ncbi_id":"253738","summary":"This gene encodes a member of the early B-cell factor (EBF) family of DNA binding transcription factors. EBF proteins are involved in B-cell differentiation, bone development and neurogenesis, and may also function as tumor suppressors. The encoded protein inhibits cell survival through the regulation of genes involved in cell cycle arrest and apoptosis, and aberrant methylation or deletion of this gene may play a role in multiple malignancies including glioblastoma multiforme and gastric carcinoma. [provided by RefSeq, Sep 2011]","start":129835283,"end":129963841,"strand":-1,"description":"early B-cell factor 3 [Source:HGNC Symbol;Acc:HGNC:19087]"}, {"versioned_ensembl_gene_id":"ENSG00000169946.13","gene_symbol":"ZFPM2","gene_name":"zinc finger protein, FOG family member 2 [Source:HGNC Symbol;Acc:HGNC:16700]","synonyms":"hFOG-2,FOG2,ZNF89B,ZC2HC11B","biotype":"protein_coding","ncbi_id":"23414","summary":"The zinc finger protein encoded by this gene is a widely expressed member of the FOG family of transcription factors. The family members modulate the activity of GATA family proteins, which are important regulators of hematopoiesis and cardiogenesis in mammals. It has been demonstrated that the protein can both activate and down-regulate expression of GATA-target genes, suggesting different modulation in different promoter contexts. A related mRNA suggests an alternatively spliced product but this information is not yet fully supported by the sequence. [provided by RefSeq, Jul 2008]","start":104590733,"end":105804532,"strand":1,"description":"zinc finger protein, FOG family member 2 [Source:HGNC Symbol;Acc:HGNC:16700]"}, {"versioned_ensembl_gene_id":"ENSG00000227046.8","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"protein_coding","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33240162,"end":33250873,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000127528.5","gene_symbol":"KLF2","gene_name":"Kruppel like factor 2 [Source:HGNC Symbol;Acc:HGNC:6347]","synonyms":"LKLF","biotype":"protein_coding","ncbi_id":"10365","summary":"This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is expressed early in mammalian development and is found in many different cell types. The protein acts to bind the CACCC box found in the promoter of target genes to activate their transcription. It plays a role in many processes during development and disease including adipogenesis, embryonic erythropoiesis, epithelial integrity, inflammation and t-cell viability. [provided by RefSeq, Mar 2017]","start":16324817,"end":16327874,"strand":1,"description":"Kruppel like factor 2 [Source:HGNC Symbol;Acc:HGNC:6347]"}, {"versioned_ensembl_gene_id":"ENSG00000151470.12","gene_symbol":"C4orf33","gene_name":"chromosome 4 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:27025]","synonyms":"FLJ33703","biotype":"protein_coding","ncbi_id":"132321","summary":null,"start":129093317,"end":129116640,"strand":1,"description":"chromosome 4 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:27025]"}, {"versioned_ensembl_gene_id":"ENSG00000180251.4","gene_symbol":"SLC9A4","gene_name":"solute carrier family 9 member A4 [Source:HGNC Symbol;Acc:HGNC:11077]","synonyms":"NHE4","biotype":"protein_coding","ncbi_id":"389015","summary":null,"start":102473303,"end":102533972,"strand":1,"description":"solute carrier family 9 member A4 [Source:HGNC Symbol;Acc:HGNC:11077]"}, {"versioned_ensembl_gene_id":"ENSG00000236577.1","gene_symbol":"SNRPGP14","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42039]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874434","summary":null,"start":49488970,"end":49489364,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42039]"}, {"versioned_ensembl_gene_id":"ENSG00000215378.3","gene_symbol":"DEFT1P","gene_name":"defensin, theta 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:18339]","synonyms":"DEFT1,DEFQ1","biotype":"unprocessed_pseudogene","ncbi_id":"170949","summary":null,"start":6987178,"end":6989721,"strand":-1,"description":"defensin, theta 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:18339]"}, {"versioned_ensembl_gene_id":"ENSG00000236091.1","gene_symbol":"LINC02243","gene_name":"long intergenic non-protein coding RNA 2243 [Source:HGNC Symbol;Acc:HGNC:53129]","synonyms":"ENST00000441841","biotype":"lincRNA","ncbi_id":"340581","summary":null,"start":134949549,"end":134953382,"strand":1,"description":"long intergenic non-protein coding RNA 2243 [Source:HGNC Symbol;Acc:HGNC:53129]"}, {"versioned_ensembl_gene_id":"ENSG00000266126.1","gene_symbol":"AC005730.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19929372,"end":19929737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231929.2","gene_symbol":"HMGB3P31","gene_name":"high mobility group box 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392545","summary":null,"start":134961711,"end":134962305,"strand":-1,"description":"high mobility group box 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39334]"}, {"versioned_ensembl_gene_id":"ENSG00000277825.1","gene_symbol":"AC020917.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16352462,"end":16353182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232395.1","gene_symbol":"AL138830.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114477350,"end":114488752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184785.5","gene_symbol":"SMIM10","gene_name":"small integral membrane protein 10 [Source:HGNC Symbol;Acc:HGNC:41913]","synonyms":"CXorf69","biotype":"protein_coding","ncbi_id":"644538","summary":null,"start":134990938,"end":134992473,"strand":1,"description":"small integral membrane protein 10 [Source:HGNC Symbol;Acc:HGNC:41913]"}, {"versioned_ensembl_gene_id":"ENSG00000255331.1","gene_symbol":"AP000790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60077350,"end":60078401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236719.2","gene_symbol":"OVAAL","gene_name":"ovarian adenocarcinoma amplified long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49422]","synonyms":"LINC01131,OVAL","biotype":"lincRNA","ncbi_id":"148756","summary":null,"start":180558976,"end":180566518,"strand":1,"description":"ovarian adenocarcinoma amplified long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49422]"}, {"versioned_ensembl_gene_id":"ENSG00000226079.1","gene_symbol":"AL138830.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114523451,"end":114535875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219619.2","gene_symbol":"AL606845.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115358498,"end":115358752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128872.9","gene_symbol":"TMOD2","gene_name":"tropomodulin 2 [Source:HGNC Symbol;Acc:HGNC:11872]","synonyms":"NTMOD","biotype":"protein_coding","ncbi_id":"29767","summary":"This gene encodes a neuronal-specific member of the tropomodulin family of actin-regulatory proteins. The encoded protein caps the pointed end of actin filaments preventing both elongation and depolymerization. The capping activity of this protein is dependent on its association with tropomyosin. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Dec 2008]","start":51751561,"end":51816368,"strand":1,"description":"tropomodulin 2 [Source:HGNC Symbol;Acc:HGNC:11872]"}, {"versioned_ensembl_gene_id":"ENSG00000181617.5","gene_symbol":"FDCSP","gene_name":"follicular dendritic cell secreted protein [Source:HGNC Symbol;Acc:HGNC:19215]","synonyms":"FDC-SP,C4orf7","biotype":"protein_coding","ncbi_id":"260436","summary":"This gene encodes a small secreted protein that is expressed in follicular dendritic cells. This protein specifically binds to activated B cells, and functions as a regulator of antibody responses. It is also thought to contribute to tumor metastases by promoting cancer cell migration and invasion. [provided by RefSeq, Dec 2011]","start":70226071,"end":70235252,"strand":1,"description":"follicular dendritic cell secreted protein [Source:HGNC Symbol;Acc:HGNC:19215]"}, {"versioned_ensembl_gene_id":"ENSG00000260461.1","gene_symbol":"AL133355.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":103877374,"end":103879761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149534.8","gene_symbol":"MS4A2","gene_name":"membrane spanning 4-domains A2 [Source:HGNC Symbol;Acc:HGNC:7316]","synonyms":"MS4A1,IGER,FCER1B,APY","biotype":"protein_coding","ncbi_id":"2206","summary":"The allergic response involves the binding of allergen to receptor-bound IgE followed by cell activation and the release of mediators responsible for the manifestations of allergy. The IgE-receptor, a tetramer composed of an alpha, beta, and 2 disulfide-linked gamma chains, is found on the surface of mast cells and basophils. This gene encodes the beta subunit of the high affinity IgE receptor which is a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This family member is localized to 11q12, among a cluster of membrane-spanning 4A gene family members. Alternative splicing results in multiple transcript variants encoding distinct proteins. Additional transcript variants have been described but require experimental validation. [provided by RefSeq, Mar 2012]","start":60088261,"end":60098466,"strand":1,"description":"membrane spanning 4-domains A2 [Source:HGNC Symbol;Acc:HGNC:7316]"}, {"versioned_ensembl_gene_id":"ENSG00000228777.1","gene_symbol":"LINC02534","gene_name":"long intergenic non-protein coding RNA 2534 [Source:HGNC Symbol;Acc:HGNC:53567]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377962","summary":null,"start":115633542,"end":115634191,"strand":-1,"description":"long intergenic non-protein coding RNA 2534 [Source:HGNC Symbol;Acc:HGNC:53567]"}, {"versioned_ensembl_gene_id":"ENSG00000251276.1","gene_symbol":"MAGI2-AS1","gene_name":"MAGI2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40860]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874020","summary":null,"start":78939850,"end":78940895,"strand":1,"description":"MAGI2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40860]"}, {"versioned_ensembl_gene_id":"ENSG00000100209.9","gene_symbol":"HSCB","gene_name":"HscB mitochondrial iron-sulfur cluster cochaperone [Source:HGNC Symbol;Acc:HGNC:28913]","synonyms":"DNAJC20,Jac1,HSC20","biotype":"protein_coding","ncbi_id":"150274","summary":"This gene encodes a DnaJ-type co-chaperone and member of the heat shock cognate B (HscB) family of proteins. The encoded protein plays a role in the synthesis of iron-sulfur clusters, protein cofactors that are involved in the redox reactions of mitochondrial electron transport and other processes. Cells in which this gene is knocked down exhibit reduced activity of iron-sulfur cluster-dependent enzymes including succinate dehydrogenase and aconitase. The encoded protein may stimulate the ATPase activity of the mitochondrial stress-70 protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":28742031,"end":28757515,"strand":1,"description":"HscB mitochondrial iron-sulfur cluster cochaperone [Source:HGNC Symbol;Acc:HGNC:28913]"}, {"versioned_ensembl_gene_id":"ENSG00000281120.1","gene_symbol":"AC006355.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79139829,"end":79177210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107960.10","gene_symbol":"STN1","gene_name":"STN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:26200]","synonyms":"FLJ22559,bA541N10.2,OBFC1","biotype":"protein_coding","ncbi_id":"79991","summary":"OBFC1 and C17ORF68 (MIM 613129) are subunits of an alpha accessory factor (AAF) that stimulates the activity of DNA polymerase-alpha-primase (see MIM 176636), the enzyme that initiates DNA replication (Casteel et al., 2009 [PubMed 19119139]). OBFC1 also appears to function in a telomere-associated complex with C17ORF68 and TEN1 (C17ORF106; MIM 613130) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009]","start":103882542,"end":103918205,"strand":-1,"description":"STN1, CST complex subunit [Source:HGNC Symbol;Acc:HGNC:26200]"}, {"versioned_ensembl_gene_id":"ENSG00000104549.11","gene_symbol":"SQLE","gene_name":"squalene epoxidase [Source:HGNC Symbol;Acc:HGNC:11279]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6713","summary":"Squalene epoxidase catalyzes the first oxygenation step in sterol biosynthesis and is thought to be one of the rate-limiting enzymes in this pathway. [provided by RefSeq, Jul 2008]","start":124998497,"end":125022283,"strand":1,"description":"squalene epoxidase [Source:HGNC Symbol;Acc:HGNC:11279]"}, {"versioned_ensembl_gene_id":"ENSG00000187391.19","gene_symbol":"MAGI2","gene_name":"membrane associated guanylate kinase, WW and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18957]","synonyms":"MAGI-2,KIAA0705,ARIP1,AIP1,ACVRIP1","biotype":"protein_coding","ncbi_id":"9863","summary":"The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family. [provided by RefSeq, Jul 2008]","start":78017057,"end":79453574,"strand":-1,"description":"membrane associated guanylate kinase, WW and PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18957]"}, {"versioned_ensembl_gene_id":"ENSG00000275327.1","gene_symbol":"AL354950.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129837505,"end":129837794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147905.17","gene_symbol":"ZCCHC7","gene_name":"zinc finger CCHC-type containing 7 [Source:HGNC Symbol;Acc:HGNC:26209]","synonyms":"FLJ22611,AIR1","biotype":"protein_coding","ncbi_id":"84186","summary":null,"start":37120539,"end":37358149,"strand":1,"description":"zinc finger CCHC-type containing 7 [Source:HGNC Symbol;Acc:HGNC:26209]"}, {"versioned_ensembl_gene_id":"ENSG00000151466.11","gene_symbol":"SCLT1","gene_name":"sodium channel and clathrin linker 1 [Source:HGNC Symbol;Acc:HGNC:26406]","synonyms":"hCAP-1A,FLJ30655","biotype":"protein_coding","ncbi_id":"132320","summary":"This gene encodes an adaptor protein. Studies of a related gene in rat suggest that the encoded protein functions to link clathrin to the sodium channel protein type 10 subunit alpha protein. The encoded protein has also been identified as a component of distal appendages of centrioles that is necessary for ciliogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":128864921,"end":129093607,"strand":-1,"description":"sodium channel and clathrin linker 1 [Source:HGNC Symbol;Acc:HGNC:26406]"}, {"versioned_ensembl_gene_id":"ENSG00000278668.1","gene_symbol":"AC005899.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32410159,"end":32410746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243601.1","gene_symbol":"RPL12P24","gene_name":"ribosomal protein L12 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35952]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270924","summary":null,"start":105737280,"end":105737765,"strand":-1,"description":"ribosomal protein L12 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35952]"}, {"versioned_ensembl_gene_id":"ENSG00000254041.1","gene_symbol":"AC021546.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105142860,"end":105188606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266385.1","gene_symbol":"AC005899.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32411217,"end":32412420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266981.1","gene_symbol":"AC022916.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":35188522,"end":35191343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257404.1","gene_symbol":"AC107016.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52782650,"end":52782839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267744.1","gene_symbol":"AC022916.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":35190961,"end":35191702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267782.1","gene_symbol":"AC022916.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35164243,"end":35167012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270232.1","gene_symbol":"MTCYBP22","gene_name":"mitochondrially encoded cytochrome b pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51979]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075221","summary":null,"start":100045928,"end":100046374,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51979]"}, {"versioned_ensembl_gene_id":"ENSG00000235926.1","gene_symbol":"RPS29P15","gene_name":"ribosomal protein S29 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35876]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271241","summary":null,"start":100928370,"end":100928540,"strand":1,"description":"ribosomal protein S29 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35876]"}, {"versioned_ensembl_gene_id":"ENSG00000197520.10","gene_symbol":"FAM177B","gene_name":"family with sequence similarity 177 member B [Source:HGNC Symbol;Acc:HGNC:34395]","synonyms":"RP11-452F19.2,FLJ43505","biotype":"protein_coding","ncbi_id":"400823","summary":null,"start":222737207,"end":222750805,"strand":1,"description":"family with sequence similarity 177 member B [Source:HGNC Symbol;Acc:HGNC:34395]"}, {"versioned_ensembl_gene_id":"ENSG00000232994.1","gene_symbol":"RPL7P14","gene_name":"ribosomal protein L7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35984]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129743","summary":null,"start":203040108,"end":203040899,"strand":1,"description":"ribosomal protein L7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35984]"}, {"versioned_ensembl_gene_id":"ENSG00000174837.14","gene_symbol":"ADGRE1","gene_name":"adhesion G protein-coupled receptor E1 [Source:HGNC Symbol;Acc:HGNC:3336]","synonyms":"TM7LN3,EMR1","biotype":"protein_coding","ncbi_id":"2015","summary":"This gene encodes a protein that has a domain resembling seven transmembrane G protein-coupled hormone receptors (7TM receptors) at its C-terminus. The N-terminus of the encoded protein has six EGF-like modules, separated from the transmembrane segments by a serine/threonine-rich domain, a feature reminiscent of mucin-like, single-span, integral membrane glycoproteins with adhesive properties. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":6887566,"end":6940459,"strand":1,"description":"adhesion G protein-coupled receptor E1 [Source:HGNC Symbol;Acc:HGNC:3336]"}, {"versioned_ensembl_gene_id":"ENSG00000228513.1","gene_symbol":"AC023271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203061314,"end":203062403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232989.1","gene_symbol":"AL356010.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":238268494,"end":238268595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255543.1","gene_symbol":"AP005597.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55267408,"end":55267636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125485.17","gene_symbol":"DDX31","gene_name":"DEAD-box helicase 31 [Source:HGNC Symbol;Acc:HGNC:16715]","synonyms":"FLJ14578,FLJ13633,PPP1R25,FLJ23349","biotype":"protein_coding","ncbi_id":"64794","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. The function of this member has not been determined. Alternative splicing of this gene generates multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2016]","start":132592997,"end":132670401,"strand":-1,"description":"DEAD-box helicase 31 [Source:HGNC Symbol;Acc:HGNC:16715]"}, {"versioned_ensembl_gene_id":"ENSG00000249128.1","gene_symbol":"LINC02215","gene_name":"long intergenic non-protein coding RNA 2215 [Source:HGNC Symbol;Acc:HGNC:53082]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467225","summary":null,"start":118596188,"end":118628092,"strand":1,"description":"long intergenic non-protein coding RNA 2215 [Source:HGNC Symbol;Acc:HGNC:53082]"}, {"versioned_ensembl_gene_id":"ENSG00000232043.1","gene_symbol":"AL133230.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50570975,"end":50578041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225877.1","gene_symbol":"PSG8-AS1","gene_name":"PSG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289650","summary":null,"start":42821863,"end":42826878,"strand":1,"description":"PSG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52550]"}, {"versioned_ensembl_gene_id":"ENSG00000235351.1","gene_symbol":"AC114730.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241724615,"end":241725693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204659.4","gene_symbol":"CBY3","gene_name":"chibby family member 3 [Source:HGNC Symbol;Acc:HGNC:33278]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646019","summary":null,"start":179678583,"end":179680974,"strand":-1,"description":"chibby family member 3 [Source:HGNC Symbol;Acc:HGNC:33278]"}, {"versioned_ensembl_gene_id":"ENSG00000258543.6","gene_symbol":"CR354443.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31705334,"end":31711904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231762.1","gene_symbol":"AL590426.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76660486,"end":76662770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185926.1","gene_symbol":"OR4C46","gene_name":"olfactory receptor family 4 subfamily C member 46 [Source:HGNC Symbol;Acc:HGNC:31271]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119749","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54603069,"end":54603998,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 46 [Source:HGNC Symbol;Acc:HGNC:31271]"}, {"versioned_ensembl_gene_id":"ENSG00000264743.2","gene_symbol":"DPRXP4","gene_name":"divergent-paired related homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32170]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503645","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":30975387,"end":30975954,"strand":1,"description":"divergent-paired related homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32170]"}, {"versioned_ensembl_gene_id":"ENSG00000188559.13","gene_symbol":"RALGAPA2","gene_name":"Ral GTPase activating protein catalytic alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:16207]","synonyms":"RapGAPalpha2,KIAA1272,dJ1049G11.4,C20orf74,AS250","biotype":"protein_coding","ncbi_id":"57186","summary":null,"start":20389552,"end":20712488,"strand":-1,"description":"Ral GTPase activating protein catalytic alpha subunit 2 [Source:HGNC Symbol;Acc:HGNC:16207]"}, {"versioned_ensembl_gene_id":"ENSG00000239809.1","gene_symbol":"AC008026.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62381668,"end":62382015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111325.16","gene_symbol":"OGFOD2","gene_name":"2-oxoglutarate and iron dependent oxygenase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25823]","synonyms":"FLJ37501,FLJ13491","biotype":"protein_coding","ncbi_id":"79676","summary":null,"start":122974580,"end":122980043,"strand":1,"description":"2-oxoglutarate and iron dependent oxygenase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25823]"}, {"versioned_ensembl_gene_id":"ENSG00000130948.9","gene_symbol":"HSD17B3","gene_name":"hydroxysteroid 17-beta dehydrogenase 3 [Source:HGNC Symbol;Acc:HGNC:5212]","synonyms":"SDR12C2","biotype":"protein_coding","ncbi_id":"3293","summary":"This isoform of 17 beta-hydroxysteroid dehydrogenase is expressed predominantly in the testis and catalyzes the conversion of androstenedione to testosterone. It preferentially uses NADP as cofactor. Deficiency can result in male pseudohermaphroditism with gynecomastia. [provided by RefSeq, Jul 2008]","start":96235306,"end":96302152,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 3 [Source:HGNC Symbol;Acc:HGNC:5212]"}, {"versioned_ensembl_gene_id":"ENSG00000232283.1","gene_symbol":"HSD17B3-AS1","gene_name":"HSD17B3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53136]","synonyms":"ENST00000448857","biotype":"antisense_RNA","ncbi_id":"105376162","summary":null,"start":96246462,"end":96250393,"strand":1,"description":"HSD17B3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53136]"}, {"versioned_ensembl_gene_id":"ENSG00000279810.1","gene_symbol":"AL109924.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":169033381,"end":169034050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231225.9","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31393526,"end":31409981,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000273061.1","gene_symbol":"CDC37L1-AS1","gene_name":"CDC37L1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49735]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929351","summary":null,"start":4676600,"end":4679502,"strand":-1,"description":"CDC37L1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49735]"}, {"versioned_ensembl_gene_id":"ENSG00000084628.9","gene_symbol":"NKAIN1","gene_name":"sodium/potassium transporting ATPase interacting 1 [Source:HGNC Symbol;Acc:HGNC:25743]","synonyms":"FLJ12650,FAM77C","biotype":"protein_coding","ncbi_id":"79570","summary":"NKAIN1 is a member of a family of mammalian proteins with similarity to Drosophila Nkain and interacts with the beta subunit of Na,K-ATPase (ATP1B1; MIM 182330) (Gorokhova et al., 2007 [PubMed 17606467]).[supplied by OMIM, Jun 2009]","start":31179745,"end":31239554,"strand":-1,"description":"sodium/potassium transporting ATPase interacting 1 [Source:HGNC Symbol;Acc:HGNC:25743]"}, {"versioned_ensembl_gene_id":"ENSG00000178950.16","gene_symbol":"GAK","gene_name":"cyclin G associated kinase [Source:HGNC Symbol;Acc:HGNC:4113]","synonyms":"DNAJC26","biotype":"protein_coding","ncbi_id":"2580","summary":"In all eukaryotes, the cell cycle is governed by cyclin-dependent protein kinases (CDKs), whose activities are regulated by cyclins and CDK inhibitors in a diverse array of mechanisms that involve the control of phosphorylation and dephosphorylation of Ser, Thr or Tyr residues. Cyclins are molecules that possess a consensus domain called the 'cyclin box.' In mammalian cells, 9 cyclin species have been identified, and they are referred to as cyclins A through I. Cyclin G is a direct transcriptional target of the p53 tumor suppressor gene product and thus functions downstream of p53. GAK is an association partner of cyclin G and CDK5. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":849276,"end":932373,"strand":-1,"description":"cyclin G associated kinase [Source:HGNC Symbol;Acc:HGNC:4113]"}, {"versioned_ensembl_gene_id":"ENSG00000196323.12","gene_symbol":"ZBTB44","gene_name":"zinc finger and BTB domain containing 44 [Source:HGNC Symbol;Acc:HGNC:25001]","synonyms":"ZNF851,HSPC063,BTBD15","biotype":"protein_coding","ncbi_id":"29068","summary":null,"start":130226677,"end":130314686,"strand":-1,"description":"zinc finger and BTB domain containing 44 [Source:HGNC Symbol;Acc:HGNC:25001]"}, {"versioned_ensembl_gene_id":"ENSG00000107281.9","gene_symbol":"NPDC1","gene_name":"neural proliferation, differentiation and control 1 [Source:HGNC Symbol;Acc:HGNC:7899]","synonyms":"DKFZp586J0523,CAB1,CAB-","biotype":"protein_coding","ncbi_id":"56654","summary":null,"start":137039470,"end":137046203,"strand":-1,"description":"neural proliferation, differentiation and control 1 [Source:HGNC Symbol;Acc:HGNC:7899]"}, {"versioned_ensembl_gene_id":"ENSG00000283605.1","gene_symbol":"AC110057.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50018798,"end":50019695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227869.1","gene_symbol":"AC073486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125431347,"end":125466401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106803.9","gene_symbol":"SEC61B","gene_name":"Sec61 translocon beta subunit [Source:HGNC Symbol;Acc:HGNC:16993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10952","summary":"The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. Oligomers of the Sec61 complex form a transmembrane channel where proteins are translocated across and integrated into the ER membrane. This complex consists of three membrane proteins- alpha, beta, and gamma. This gene encodes the beta-subunit protein. The Sec61 subunits are also observed in the post-ER compartment, suggesting that these proteins can escape the ER and recycle back. There is evidence for multiple polyadenylated sites for this transcript. [provided by RefSeq, Jul 2008]","start":99222064,"end":99230615,"strand":1,"description":"Sec61 translocon beta subunit [Source:HGNC Symbol;Acc:HGNC:16993]"}, {"versioned_ensembl_gene_id":"ENSG00000254625.1","gene_symbol":"AF233439.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6928608,"end":6930473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122971.8","gene_symbol":"ACADS","gene_name":"acyl-CoA dehydrogenase, C-2 to C-3 short chain [Source:HGNC Symbol;Acc:HGNC:90]","synonyms":"SCAD,ACAD3","biotype":"protein_coding","ncbi_id":"35","summary":"This gene encodes a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with short-chain acyl-CoA dehydrogenase (SCAD) deficiency. Alternative splicing results in two variants which encode different isoforms. [provided by RefSeq, Oct 2014]","start":120725735,"end":120740008,"strand":1,"description":"acyl-CoA dehydrogenase, C-2 to C-3 short chain [Source:HGNC Symbol;Acc:HGNC:90]"}, {"versioned_ensembl_gene_id":"ENSG00000145868.16","gene_symbol":"FBXO38","gene_name":"F-box protein 38 [Source:HGNC Symbol;Acc:HGNC:28844]","synonyms":"Fbx38,SP329,MOKA,FLJ13962","biotype":"protein_coding","ncbi_id":"81545","summary":"This gene encodes a large protein that contains an F-box domain and may participate in protein ubiquitination. The encoded protein is a transcriptional co-activator of Krueppel-like factor 7 (Klf7). A heterozygous mutation in this gene was found in individuals with autosomal dominant distal hereditary motor neuronopathy type IID. There is a pseudogene for this gene on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":148383935,"end":148442836,"strand":1,"description":"F-box protein 38 [Source:HGNC Symbol;Acc:HGNC:28844]"}, {"versioned_ensembl_gene_id":"ENSG00000237927.1","gene_symbol":"AL078604.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159586955,"end":159589169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230700.9","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb1,Ckb2","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31647414,"end":31654461,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000250079.1","gene_symbol":"AC093300.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28213359,"end":28214559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224736.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29787843,"end":29794717,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000033327.12","gene_symbol":"GAB2","gene_name":"GRB2 associated binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14458]","synonyms":"KIAA0571","biotype":"protein_coding","ncbi_id":"9846","summary":"This gene is a member of the GRB2-associated binding protein (GAB) gene family. These proteins contain pleckstrin homology (PH) domain, and bind SHP2 tyrosine phosphatase and GRB2 adapter protein. They act as adapters for transmitting various signals in response to stimuli through cytokine and growth factor receptors, and T- and B-cell antigen receptors. The protein encoded by this gene is the principal activator of phosphatidylinositol-3 kinase in response to activation of the high affinity IgE receptor. Two alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Nov 2009]","start":78215297,"end":78418348,"strand":-1,"description":"GRB2 associated binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14458]"}, {"versioned_ensembl_gene_id":"ENSG00000233954.6","gene_symbol":"UQCRHL","gene_name":"ubiquinol-cytochrome c reductase hinge protein like [Source:HGNC Symbol;Acc:HGNC:51714]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440567","summary":"This gene has characteristics of a pseudogene derived from the UQCRH gene. However, there is still an open reading frame that could produce a protein of the same or nearly the same size as that of the UQCRH gene, so this gene is being called protein-coding for now. [provided by RefSeq, Jul 2008]","start":15807169,"end":15809348,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein like [Source:HGNC Symbol;Acc:HGNC:51714]"}, {"versioned_ensembl_gene_id":"ENSG00000254733.1","gene_symbol":"AP001831.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86431590,"end":86622867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272027.2","gene_symbol":"AC073218.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34692290,"end":34703606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260771.1","gene_symbol":"AL138918.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168374697,"end":168375355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255067.1","gene_symbol":"AC013549.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12848795,"end":12849433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108523.15","gene_symbol":"RNF167","gene_name":"ring finger protein 167 [Source:HGNC Symbol;Acc:HGNC:24544]","synonyms":"DKFZP566H073","biotype":"protein_coding","ncbi_id":"26001","summary":"RNF167 is an E3 ubiquitin ligase that interacts with TSSC5 (SLC22A18; MIM 602631) and, together with UBCH6 (UBE2E1; MIM 602916), facilitates TSSC5 polyubiquitylation (Yamada and Gorbsky, 2006 [PubMed 16314844]).[supplied by OMIM, Mar 2008]","start":4940008,"end":4945222,"strand":1,"description":"ring finger protein 167 [Source:HGNC Symbol;Acc:HGNC:24544]"}, {"versioned_ensembl_gene_id":"ENSG00000203258.3","gene_symbol":"AC013549.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12921186,"end":12922925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270797.1","gene_symbol":"AC004987.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39788967,"end":39789304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251400.1","gene_symbol":"ALDH7A1P1","gene_name":"aldehyde dehydrogenase 7 family member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:878]","synonyms":"ATQL1","biotype":"processed_pseudogene","ncbi_id":"541","summary":null,"start":77290268,"end":77291800,"strand":1,"description":"aldehyde dehydrogenase 7 family member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:878]"}, {"versioned_ensembl_gene_id":"ENSG00000127318.10","gene_symbol":"IL22","gene_name":"interleukin 22 [Source:HGNC Symbol;Acc:HGNC:14900]","synonyms":"IL-22,IL-21,zcyto18,TIFIL-23,TIFa,MGC79384,MGC79382,ILTIF,IL-TIF,IL-D110","biotype":"protein_coding","ncbi_id":"50616","summary":"This gene is a member of the IL10 family of cytokines that mediate cellular inflammatory responses. The encoded protein functions in antimicrobial defense at mucosal surfaces and in tissue repair. This protein also has pro-inflammatory properties and plays a role in in the pathogenesis of several intestinal diseases. [provided by RefSeq, Jul 2018]","start":68248242,"end":68253607,"strand":-1,"description":"interleukin 22 [Source:HGNC Symbol;Acc:HGNC:14900]"}, {"versioned_ensembl_gene_id":"ENSG00000282456.1","gene_symbol":"LINC02210-CRHR1","gene_name":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104909134","summary":"This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene. [provided by RefSeq, Dec 2016]","start":45633529,"end":45828162,"strand":1,"description":"LINC02210-CRHR1 readthrough [Source:HGNC Symbol;Acc:HGNC:51483]"}, {"versioned_ensembl_gene_id":"ENSG00000130561.16","gene_symbol":"SAG","gene_name":"S-antigen visual arrestin [Source:HGNC Symbol;Acc:HGNC:10521]","synonyms":"RP47,ARRESTIN","biotype":"protein_coding","ncbi_id":"6295","summary":"Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness. [provided by RefSeq, Jul 2008]","start":233307816,"end":233347055,"strand":1,"description":"S-antigen visual arrestin [Source:HGNC Symbol;Acc:HGNC:10521]"}, {"versioned_ensembl_gene_id":"ENSG00000251122.1","gene_symbol":"NIFKP2","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44950]","synonyms":"MKI67IPP2","biotype":"processed_pseudogene","ncbi_id":"645398","summary":null,"start":174923090,"end":174923945,"strand":1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44950]"}, {"versioned_ensembl_gene_id":"ENSG00000163069.12","gene_symbol":"SGCB","gene_name":"sarcoglycan beta [Source:HGNC Symbol;Acc:HGNC:10806]","synonyms":"SGC,LGMD2E,A3b","biotype":"protein_coding","ncbi_id":"6443","summary":"This gene encodes a member of the sarcoglycan family. Sarcoglycans are transmembrane components in the dystrophin-glycoprotein complex which help stabilize the muscle fiber membranes and link the muscle cytoskeleton to the extracellular matrix. Mutations in this gene have been associated with limb-girdle muscular dystrophy.[provided by RefSeq, Oct 2008]","start":52020706,"end":52038482,"strand":-1,"description":"sarcoglycan beta [Source:HGNC Symbol;Acc:HGNC:10806]"}, {"versioned_ensembl_gene_id":"ENSG00000149201.9","gene_symbol":"CCDC81","gene_name":"coiled-coil domain containing 81 [Source:HGNC Symbol;Acc:HGNC:26281]","synonyms":"FLJ23514,FLJ16339","biotype":"protein_coding","ncbi_id":"60494","summary":null,"start":86374736,"end":86423109,"strand":1,"description":"coiled-coil domain containing 81 [Source:HGNC Symbol;Acc:HGNC:26281]"}, {"versioned_ensembl_gene_id":"ENSG00000087085.13","gene_symbol":"ACHE","gene_name":"acetylcholinesterase (Cartwright blood group) [Source:HGNC Symbol;Acc:HGNC:108]","synonyms":"YT","biotype":"protein_coding","ncbi_id":"43","summary":"Acetylcholinesterase hydrolyzes the neurotransmitter, acetylcholine at neuromuscular junctions and brain cholinergic synapses, and thus terminates signal transmission. It is also found on the red blood cell membranes, where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties, but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene, and the structural diversity in the gene products arises from alternative mRNA splicing, and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain, muscle and other tissues is the hydrophilic species, which forms disulfide-linked oligomers with collagenous, or lipid-containing structural subunits. The other, alternatively spliced form, expressed primarily in the erythroid tissues, differs at the C-terminal end, and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally. AChE activity may constitute a sensitive biomarker of RBC ageing in vivo, and thus, may be of aid in understanding the effects of transfusion[provided by RefSeq, Sep 2019]","start":100889994,"end":100896974,"strand":-1,"description":"acetylcholinesterase (Cartwright blood group) [Source:HGNC Symbol;Acc:HGNC:108]"}, {"versioned_ensembl_gene_id":"ENSG00000249004.1","gene_symbol":"PRMT5P1","gene_name":"protein arginine methyltransferase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32524]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420927","summary":null,"start":147458724,"end":147459321,"strand":-1,"description":"protein arginine methyltransferase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32524]"}, {"versioned_ensembl_gene_id":"ENSG00000037897.16","gene_symbol":"METTL1","gene_name":"methyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:7030]","synonyms":"TRMT8,TRM8,C12orf1","biotype":"protein_coding","ncbi_id":"4234","summary":"This gene is similar in sequence to the S. cerevisiae YDL201w gene. The gene product contains a conserved S-adenosylmethionine-binding motif and is inactivated by phosphorylation. Alternative splice variants encoding different protein isoforms have been described for this gene. A pseudogene has been identified on chromosome X. [provided by RefSeq, Jul 2008]","start":57768471,"end":57772793,"strand":-1,"description":"methyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:7030]"}, {"versioned_ensembl_gene_id":"ENSG00000253454.1","gene_symbol":"NDUFA5P2","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724035","summary":null,"start":104566086,"end":104566429,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48855]"}, {"versioned_ensembl_gene_id":"ENSG00000205659.10","gene_symbol":"LIN52","gene_name":"lin-52 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:19856]","synonyms":"C14orf46","biotype":"protein_coding","ncbi_id":"91750","summary":null,"start":74084796,"end":74201235,"strand":1,"description":"lin-52 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:19856]"}, {"versioned_ensembl_gene_id":"ENSG00000243445.1","gene_symbol":"AC106820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2332313,"end":2332732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169299.13","gene_symbol":"PGM2","gene_name":"phosphoglucomutase 2 [Source:HGNC Symbol;Acc:HGNC:8906]","synonyms":"FLJ10983","biotype":"protein_coding","ncbi_id":"55276","summary":null,"start":37826633,"end":37862937,"strand":1,"description":"phosphoglucomutase 2 [Source:HGNC Symbol;Acc:HGNC:8906]"}, {"versioned_ensembl_gene_id":"ENSG00000274611.3","gene_symbol":"TBC1D3","gene_name":"TBC1 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:19031]","synonyms":"TBC1D3A,PRC17,DKFZp434P2235","biotype":"protein_coding","ncbi_id":"729873","summary":null,"start":38181659,"end":38192541,"strand":-1,"description":"TBC1 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:19031]"}, {"versioned_ensembl_gene_id":"ENSG00000155380.11","gene_symbol":"SLC16A1","gene_name":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]","synonyms":"MCT1,MCT","biotype":"protein_coding","ncbi_id":"6566","summary":"The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]","start":112911847,"end":112957013,"strand":-1,"description":"solute carrier family 16 member 1 [Source:HGNC Symbol;Acc:HGNC:10922]"}, {"versioned_ensembl_gene_id":"ENSG00000274419.6","gene_symbol":"TBC1D3D","gene_name":"TBC1 domain family member 3D [Source:HGNC Symbol;Acc:HGNC:28944]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060389","summary":null,"start":38003976,"end":38014902,"strand":1,"description":"TBC1 domain family member 3D [Source:HGNC Symbol;Acc:HGNC:28944]"}, {"versioned_ensembl_gene_id":"ENSG00000114867.20","gene_symbol":"EIF4G1","gene_name":"eukaryotic translation initiation factor 4 gamma 1 [Source:HGNC Symbol;Acc:HGNC:3296]","synonyms":"PARK18,p220,EIF4G,EIF4F","biotype":"protein_coding","ncbi_id":"1981","summary":"The protein encoded by this gene is a component of the multi-subunit protein complex EIF4F. This complex facilitates the recruitment of mRNA to the ribosome, which is a rate-limiting step during the initiation phase of protein synthesis. The recognition of the mRNA cap and the ATP-dependent unwinding of 5'-terminal secondary structure is catalyzed by factors in this complex. The subunit encoded by this gene is a large scaffolding protein that contains binding sites for other members of the EIF4F complex. A domain at its N-terminus can also interact with the poly(A)-binding protein, which may mediate the circularization of mRNA during translation. Alternative splicing results in multiple transcript variants, some of which are derived from alternative promoter usage. [provided by RefSeq, Aug 2010]","start":184314495,"end":184335358,"strand":1,"description":"eukaryotic translation initiation factor 4 gamma 1 [Source:HGNC Symbol;Acc:HGNC:3296]"}, {"versioned_ensembl_gene_id":"ENSG00000079557.4","gene_symbol":"AFM","gene_name":"afamin [Source:HGNC Symbol;Acc:HGNC:316]","synonyms":"ALBA,ALB2","biotype":"protein_coding","ncbi_id":"173","summary":"This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream. [provided by RefSeq, Jul 2008]","start":73481683,"end":73504001,"strand":1,"description":"afamin [Source:HGNC Symbol;Acc:HGNC:316]"}, {"versioned_ensembl_gene_id":"ENSG00000223593.1","gene_symbol":"AL356806.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34416687,"end":34417602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104866.10","gene_symbol":"PPP1R37","gene_name":"protein phosphatase 1 regulatory subunit 37 [Source:HGNC Symbol;Acc:HGNC:27607]","synonyms":"LRRC68","biotype":"protein_coding","ncbi_id":"284352","summary":null,"start":45091396,"end":45148077,"strand":1,"description":"protein phosphatase 1 regulatory subunit 37 [Source:HGNC Symbol;Acc:HGNC:27607]"}, {"versioned_ensembl_gene_id":"ENSG00000213798.3","gene_symbol":"AC004129.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25212170,"end":25212965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250482.3","gene_symbol":"DUX4L51","gene_name":"double homeobox 4 like 51 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51810]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481740","summary":null,"start":31249879,"end":31250987,"strand":1,"description":"double homeobox 4 like 51 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51810]"}, {"versioned_ensembl_gene_id":"ENSG00000226107.1","gene_symbol":"AC004383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134522702,"end":134522990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278784.1","gene_symbol":"AL136295.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24201612,"end":24202811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254692.1","gene_symbol":"AL136295.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24189157,"end":24213473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253421.1","gene_symbol":"ZNHIT1P1","gene_name":"zinc finger HIT-type containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288248","summary":null,"start":142858354,"end":142858797,"strand":1,"description":"zinc finger HIT-type containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44474]"}, {"versioned_ensembl_gene_id":"ENSG00000235832.2","gene_symbol":"CNN2P3","gene_name":"calponin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39528]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392343","summary":null,"start":64486164,"end":64487069,"strand":-1,"description":"calponin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39528]"}, {"versioned_ensembl_gene_id":"ENSG00000277449.1","gene_symbol":"CEBPB-AS1","gene_name":"CEBPB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51226]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927559","summary":null,"start":50184598,"end":50191498,"strand":-1,"description":"CEBPB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51226]"}, {"versioned_ensembl_gene_id":"ENSG00000228703.1","gene_symbol":"AL355310.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109628417,"end":109630305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237825.9","gene_symbol":"RGL2","gene_name":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]","synonyms":"KE1.5,HKE1.5,RAB2L","biotype":"protein_coding","ncbi_id":"5863","summary":null,"start":33269579,"end":33277249,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]"}, {"versioned_ensembl_gene_id":"ENSG00000230923.1","gene_symbol":"LINC00309","gene_name":"long intergenic non-protein coding RNA 309 [Source:HGNC Symbol;Acc:HGNC:25279]","synonyms":"NCRNA00309","biotype":"lincRNA","ncbi_id":"150992","summary":null,"start":64185078,"end":64205485,"strand":-1,"description":"long intergenic non-protein coding RNA 309 [Source:HGNC Symbol;Acc:HGNC:25279]"}, {"versioned_ensembl_gene_id":"ENSG00000266573.5","gene_symbol":"AC018697.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24725781,"end":24929076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245857.2","gene_symbol":"GS1-24F4.2","gene_name":"uncharacterized LOC100652791 [Source:NCBI gene;Acc:100652791]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652791","summary":null,"start":6835554,"end":6885276,"strand":1,"description":"uncharacterized LOC100652791 [Source:NCBI gene;Acc:100652791]"}, {"versioned_ensembl_gene_id":"ENSG00000167618.9","gene_symbol":"LAIR2","gene_name":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]","synonyms":"CD306","biotype":"protein_coding","ncbi_id":"3904","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1, a membrane-bound receptor that modulates innate immune response. The protein encoded by this locus is a soluble receptor that may play roles in both inhibition of collagen-induced platelet aggregation and vessel formation during placental implantation. This gene maps to a region of 19q13.4, termed the leukocyte receptor cluster, which contains 29 genes in the immunoglobulin superfamily. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":54497879,"end":54510687,"strand":1,"description":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]"}, {"versioned_ensembl_gene_id":"ENSG00000243081.2","gene_symbol":"AC092894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112396647,"end":112409134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231570.1","gene_symbol":"AC008173.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56750300,"end":56750563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108344.14","gene_symbol":"PSMD3","gene_name":"proteasome 26S subunit, non-ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9560]","synonyms":"TSTA2,S3,Rpn3,P58","biotype":"protein_coding","ncbi_id":"5709","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the proteasome subunit S3 family that functions as one of the non-ATPase subunits of the 19S regulator lid. Single nucleotide polymorphisms in this gene are associated with neutrophil count. [provided by RefSeq, Jul 2012]","start":39980797,"end":39997960,"strand":1,"description":"proteasome 26S subunit, non-ATPase 3 [Source:HGNC Symbol;Acc:HGNC:9560]"}, {"versioned_ensembl_gene_id":"ENSG00000249891.2","gene_symbol":"KRT19P6","gene_name":"keratin 19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480807","summary":null,"start":91885046,"end":91885254,"strand":-1,"description":"keratin 19 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45076]"}, {"versioned_ensembl_gene_id":"ENSG00000270412.1","gene_symbol":"AL136084.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98943337,"end":98943775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228271.1","gene_symbol":"LINC02048","gene_name":"long intergenic non-protein coding RNA 2048 [Source:HGNC Symbol;Acc:HGNC:52888]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374289","summary":null,"start":194276682,"end":194287368,"strand":1,"description":"long intergenic non-protein coding RNA 2048 [Source:HGNC Symbol;Acc:HGNC:52888]"}, {"versioned_ensembl_gene_id":"ENSG00000276721.1","gene_symbol":"AC092375.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21833516,"end":21833621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255007.1","gene_symbol":"LINC02489","gene_name":"long intergenic non-protein coding RNA 2489 [Source:HGNC Symbol;Acc:HGNC:53470]","synonyms":"CTD-2589M5","biotype":"antisense_RNA","ncbi_id":"101928919","summary":null,"start":46256355,"end":46274547,"strand":-1,"description":"long intergenic non-protein coding RNA 2489 [Source:HGNC Symbol;Acc:HGNC:53470]"}, {"versioned_ensembl_gene_id":"ENSG00000187033.9","gene_symbol":"SAMD7","gene_name":"sterile alpha motif domain containing 7 [Source:HGNC Symbol;Acc:HGNC:25394]","synonyms":"DKFZp686E1583","biotype":"protein_coding","ncbi_id":"344658","summary":null,"start":169911572,"end":169939175,"strand":1,"description":"sterile alpha motif domain containing 7 [Source:HGNC Symbol;Acc:HGNC:25394]"}, {"versioned_ensembl_gene_id":"ENSG00000117152.13","gene_symbol":"RGS4","gene_name":"regulator of G protein signaling 4 [Source:HGNC Symbol;Acc:HGNC:10000]","synonyms":"SCZD9","biotype":"protein_coding","ncbi_id":"5999","summary":"Regulator of G protein signaling (RGS) family members are regulatory molecules that act as GTPase activating proteins (GAPs) for G alpha subunits of heterotrimeric G proteins. RGS proteins are able to deactivate G protein subunits of the Gi alpha, Go alpha and Gq alpha subtypes. They drive G proteins into their inactive GDP-bound forms. Regulator of G protein signaling 4 belongs to this family. All RGS proteins share a conserved 120-amino acid sequence termed the RGS domain. Regulator of G protein signaling 4 protein is 37% identical to RGS1 and 97% identical to rat Rgs4. This protein negatively regulate signaling upstream or at the level of the heterotrimeric G protein and is localized in the cytoplasm. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":163068775,"end":163076802,"strand":1,"description":"regulator of G protein signaling 4 [Source:HGNC Symbol;Acc:HGNC:10000]"}, {"versioned_ensembl_gene_id":"ENSG00000282418.1","gene_symbol":"AC092811.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":225465021,"end":225473837,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263317.1","gene_symbol":"LINC01982","gene_name":"long intergenic non-protein coding RNA 1982 [Source:HGNC Symbol;Acc:HGNC:52812]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371830","summary":null,"start":52390515,"end":52535701,"strand":1,"description":"long intergenic non-protein coding RNA 1982 [Source:HGNC Symbol;Acc:HGNC:52812]"}, {"versioned_ensembl_gene_id":"ENSG00000176919.11","gene_symbol":"C8G","gene_name":"complement C8 gamma chain [Source:HGNC Symbol;Acc:HGNC:1354]","synonyms":null,"biotype":"protein_coding","ncbi_id":"733","summary":"The protein encoded by this gene belongs to the lipocalin family. It is one of the three subunits that constitutes complement component 8 (C8), which is composed of a disulfide-linked C8 alpha-gamma heterodimer and a non-covalently associated C8 beta chain. C8 participates in the formation of the membrane attack complex (MAC) on bacterial cell membranes. While subunits alpha and beta play a role in complement-mediated bacterial killing, the gamma subunit is not required for the bactericidal activity. [provided by RefSeq, Jul 2011]","start":136945246,"end":136946974,"strand":1,"description":"complement C8 gamma chain [Source:HGNC Symbol;Acc:HGNC:1354]"}, {"versioned_ensembl_gene_id":"ENSG00000177725.5","gene_symbol":"AC105206.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":22169338,"end":22171710,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230763.11","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33109380,"end":33120645,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000283992.1","gene_symbol":"SLURP2","gene_name":"secreted LY6/PLAUR domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25549]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":142764338,"end":142769844,"strand":-1,"description":"secreted LY6/PLAUR domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25549]"}, {"versioned_ensembl_gene_id":"ENSG00000283265.1","gene_symbol":"AL356234.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137693068,"end":137700415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282474.1","gene_symbol":"AL928768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105704732,"end":105705373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271742.1","gene_symbol":"AL121992.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15682873,"end":15683128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050767.15","gene_symbol":"COL23A1","gene_name":"collagen type XXIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22990]","synonyms":"DKFZp434K0621","biotype":"protein_coding","ncbi_id":"91522","summary":"COL23A1 is a member of the transmembrane collagens, a subfamily of the nonfibrillar collagens that contain a single pass hydrophobic transmembrane domain (Banyard et al., 2003 [PubMed 12644459]).[supplied by OMIM, Mar 2008]","start":178237618,"end":178590555,"strand":-1,"description":"collagen type XXIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:22990]"}, {"versioned_ensembl_gene_id":"ENSG00000282094.1","gene_symbol":"IGHGP","gene_name":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]","synonyms":"IGHGP1","biotype":"IG_C_pseudogene","ncbi_id":"3505","summary":null,"start":105665404,"end":105670614,"strand":-1,"description":"immunoglobulin heavy constant gamma P (non-functional) [Source:HGNC Symbol;Acc:HGNC:5529]"}, {"versioned_ensembl_gene_id":"ENSG00000282430.1","gene_symbol":"AL928742.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105648695,"end":105649828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185641.6","gene_symbol":"AC034236.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116051917,"end":116052289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128513.14","gene_symbol":"POT1","gene_name":"protection of telomeres 1 [Source:HGNC Symbol;Acc:HGNC:17284]","synonyms":"hPot1,DKFZp586D211","biotype":"protein_coding","ncbi_id":"25913","summary":"This gene is a member of the telombin family and encodes a nuclear protein involved in telomere maintenance. Specifically, this protein functions as a member of a multi-protein complex that binds to the TTAGGG repeats of telomeres, regulating telomere length and protecting chromosome ends from illegitimate recombination, catastrophic chromosome instability, and abnormal chromosome segregation. Increased transcriptional expression of this gene is associated with stomach carcinogenesis and its progression. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]","start":124822386,"end":124929983,"strand":-1,"description":"protection of telomeres 1 [Source:HGNC Symbol;Acc:HGNC:17284]"}, {"versioned_ensembl_gene_id":"ENSG00000112210.11","gene_symbol":"RAB23","gene_name":"RAB23, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14263]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51715","summary":"This gene encodes a small GTPase of the Ras superfamily. Rab proteins are involved in the regulation of diverse cellular functions associated with intracellular membrane trafficking, including autophagy and immune response to bacterial infection. The encoded protein may play a role in central nervous system development by antagonizing sonic hedgehog signaling. Disruption of this gene has been implicated in Carpenter syndrome as well as cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":57186992,"end":57222314,"strand":-1,"description":"RAB23, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14263]"}, {"versioned_ensembl_gene_id":"ENSG00000128928.8","gene_symbol":"IVD","gene_name":"isovaleryl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:6186]","synonyms":"ACAD2","biotype":"protein_coding","ncbi_id":"3712","summary":"Isovaleryl-CoA dehydrogenase (IVD) is a mitochondrial matrix enzyme that catalyzes the third step in leucine catabolism. The genetic deficiency of IVD results in an accumulation of isovaleric acid, which is toxic to the central nervous system and leads to isovaleric acidemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]","start":40405795,"end":40435947,"strand":1,"description":"isovaleryl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:6186]"}, {"versioned_ensembl_gene_id":"ENSG00000281149.1","gene_symbol":"AP000344.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23392771,"end":23393839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187837.3","gene_symbol":"HIST1H1C","gene_name":"histone cluster 1 H1 family member c [Source:HGNC Symbol;Acc:HGNC:4716]","synonyms":"H1s-1,H1F2,H1c,H1.2","biotype":"protein_coding","ncbi_id":"3006","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26055787,"end":26056428,"strand":-1,"description":"histone cluster 1 H1 family member c [Source:HGNC Symbol;Acc:HGNC:4716]"}, {"versioned_ensembl_gene_id":"ENSG00000187504.6","gene_symbol":"RPL7P48","gene_name":"ribosomal protein L7 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:35540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388401","summary":null,"start":51502488,"end":51503233,"strand":-1,"description":"ribosomal protein L7 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:35540]"}, {"versioned_ensembl_gene_id":"ENSG00000264968.1","gene_symbol":"AC090844.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39927742,"end":39939601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255262.3","gene_symbol":"ELOBP2","gene_name":"elongin B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39720]","synonyms":"TCEB2P2","biotype":"processed_pseudogene","ncbi_id":"253665","summary":null,"start":130032866,"end":130033220,"strand":-1,"description":"elongin B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39720]"}, {"versioned_ensembl_gene_id":"ENSG00000173578.7","gene_symbol":"XCR1","gene_name":"X-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:1625]","synonyms":"GPR5,CCXCR1","biotype":"protein_coding","ncbi_id":"2829","summary":"The protein encoded by this gene is a chemokine receptor belonging to the G protein-coupled receptor superfamily. The family members are characterized by the presence of 7 transmembrane domains and numerous conserved amino acids. This receptor is most closely related to RBS11 and the MIP1-alpha/RANTES receptor. It transduces a signal by increasing the intracellular calcium ions level. The viral macrophage inflammatory protein-II is an antagonist of this receptor and blocks signaling. Several alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Apr 2020]","start":46017024,"end":46027742,"strand":-1,"description":"X-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:1625]"}, {"versioned_ensembl_gene_id":"ENSG00000260300.5","gene_symbol":"AC009119.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":83908132,"end":83951445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224861.1","gene_symbol":"YBX1P1","gene_name":"Y-box binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8015]","synonyms":"PSDBPB1,NSEP1P","biotype":"processed_pseudogene","ncbi_id":"50631","summary":null,"start":66012830,"end":66013789,"strand":-1,"description":"Y-box binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8015]"}, {"versioned_ensembl_gene_id":"ENSG00000255282.6","gene_symbol":"WTAPP1","gene_name":"Wilms tumor 1 associated protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44115]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100288077","summary":null,"start":102746968,"end":102836766,"strand":1,"description":"Wilms tumor 1 associated protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44115]"}, {"versioned_ensembl_gene_id":"ENSG00000260932.1","gene_symbol":"AC009119.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83929796,"end":83931223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229626.1","gene_symbol":"PIGCP2","gene_name":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128307","summary":null,"start":107808734,"end":107809568,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45149]"}, {"versioned_ensembl_gene_id":"ENSG00000241674.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32863344,"end":32881839,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000279676.1","gene_symbol":"AC011483.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50962197,"end":50962781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228104.1","gene_symbol":"AL935042.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32899035,"end":32899549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213022.5","gene_symbol":"KLK9","gene_name":"kallikrein related peptidase 9 [Source:HGNC Symbol;Acc:HGNC:6370]","synonyms":"KLK-L3","biotype":"protein_coding","ncbi_id":"284366","summary":"The protein encoded by this gene is a kallikrein-related serine protease. This gene is activated by steroid hormones in a human breast cancer cell line, making it a good marker for cancer detection. The encoded protein is found primarily in the cytoplasm.[provided by RefSeq, Oct 2010]","start":51003111,"end":51009634,"strand":-1,"description":"kallikrein related peptidase 9 [Source:HGNC Symbol;Acc:HGNC:6370]"}, {"versioned_ensembl_gene_id":"ENSG00000270369.1","gene_symbol":"AL591684.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47484457,"end":47484754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229724.1","gene_symbol":"OR2AQ1P","gene_name":"olfactory receptor family 2 subfamily AQ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15003]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81474","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158796014,"end":158796213,"strand":1,"description":"olfactory receptor family 2 subfamily AQ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15003]"}, {"versioned_ensembl_gene_id":"ENSG00000278630.1","gene_symbol":"LINC02335","gene_name":"long intergenic non-protein coding RNA 2335 [Source:HGNC Symbol;Acc:HGNC:53255]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984565","summary":null,"start":55062945,"end":55161490,"strand":1,"description":"long intergenic non-protein coding RNA 2335 [Source:HGNC Symbol;Acc:HGNC:53255]"}, {"versioned_ensembl_gene_id":"ENSG00000172742.5","gene_symbol":"OR4D9","gene_name":"olfactory receptor family 4 subfamily D member 9 [Source:HGNC Symbol;Acc:HGNC:15178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390199","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59511368,"end":59520703,"strand":1,"description":"olfactory receptor family 4 subfamily D member 9 [Source:HGNC Symbol;Acc:HGNC:15178]"}, {"versioned_ensembl_gene_id":"ENSG00000140332.15","gene_symbol":"TLE3","gene_name":"transducin like enhancer of split 3 [Source:HGNC Symbol;Acc:HGNC:11839]","synonyms":"KIAA1547,HsT18976,GRG3,ESG3,ESG","biotype":"protein_coding","ncbi_id":"7090","summary":"This gene encodes a transcriptional co-repressor protein that belongs to the transducin-like enhancer family of proteins. The members of this family function in the Notch signaling pathway that regulates determination of cell fate during development. Expression of this gene has been associated with a favorable outcome to chemotherapy with taxanes for ovarian carcinoma. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Sep 2013]","start":70047790,"end":70098176,"strand":-1,"description":"transducin like enhancer of split 3 [Source:HGNC Symbol;Acc:HGNC:11839]"}, {"versioned_ensembl_gene_id":"ENSG00000184305.14","gene_symbol":"CCSER1","gene_name":"coiled-coil serine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:29349]","synonyms":"KIAA1680,FAM190A","biotype":"protein_coding","ncbi_id":"401145","summary":null,"start":90127535,"end":91601913,"strand":1,"description":"coiled-coil serine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:29349]"}, {"versioned_ensembl_gene_id":"ENSG00000158545.15","gene_symbol":"ZC3H18","gene_name":"zinc finger CCCH-type containing 18 [Source:HGNC Symbol;Acc:HGNC:25091]","synonyms":"NHN1","biotype":"protein_coding","ncbi_id":"124245","summary":null,"start":88570381,"end":88631966,"strand":1,"description":"zinc finger CCCH-type containing 18 [Source:HGNC Symbol;Acc:HGNC:25091]"}, {"versioned_ensembl_gene_id":"ENSG00000244041.7","gene_symbol":"LINC01011","gene_name":"long intergenic non-protein coding RNA 1011 [Source:HGNC Symbol;Acc:HGNC:33812]","synonyms":"DKFZp686I15217","biotype":"lincRNA","ncbi_id":"401232","summary":null,"start":2987967,"end":2991173,"strand":1,"description":"long intergenic non-protein coding RNA 1011 [Source:HGNC Symbol;Acc:HGNC:33812]"}, {"versioned_ensembl_gene_id":"ENSG00000233930.3","gene_symbol":"KRTAP5-AS1","gene_name":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338651","summary":null,"start":1571353,"end":1599184,"strand":1,"description":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]"}, {"versioned_ensembl_gene_id":"ENSG00000266405.3","gene_symbol":"CBX3P2","gene_name":"chromobox 3 pseudogene 2 [Source:NCBI gene;Acc:645158]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"645158","summary":null,"start":2652170,"end":2655395,"strand":-1,"description":"chromobox 3 pseudogene 2 [Source:NCBI gene;Acc:645158]"}, {"versioned_ensembl_gene_id":"ENSG00000139648.6","gene_symbol":"KRT71","gene_name":"keratin 71 [Source:HGNC Symbol;Acc:HGNC:28927]","synonyms":"KRT6IRS1,KRT6IRS,K6IRS1","biotype":"protein_coding","ncbi_id":"112802","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes a protein that is expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]","start":52543909,"end":52553147,"strand":-1,"description":"keratin 71 [Source:HGNC Symbol;Acc:HGNC:28927]"}, {"versioned_ensembl_gene_id":"ENSG00000157782.9","gene_symbol":"CABP1","gene_name":"calcium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1384]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9478","summary":"Calcium binding proteins are an important component of calcium mediated cellular signal transduction. This gene encodes a protein that belongs to a subfamily of calcium binding proteins which share similarity to calmodulin. The protein encoded by this gene regulates the gating of voltage-gated calcium ion channels. This protein inhibits calcium-dependent inactivation and supports calcium-dependent facilitation of ion channels containing voltage-dependent L-type calcium channel subunit alpha-1C. This protein also regulates calcium-dependent activity of inositol 1,4,5-triphosphate receptors, P/Q-type voltage-gated calcium channels, and transient receptor potential channel TRPC5. This gene is predominantly expressed in retina and brain. Alternative splicing results in multiple transcript variants encoding disinct isoforms. [provided by RefSeq, Jul 2012]","start":120640552,"end":120667324,"strand":1,"description":"calcium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1384]"}, {"versioned_ensembl_gene_id":"ENSG00000251072.2","gene_symbol":"AC137794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126751963,"end":126776486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146856.14","gene_symbol":"AGBL3","gene_name":"ATP/GTP binding protein like 3 [Source:HGNC Symbol;Acc:HGNC:27981]","synonyms":"CCP3,MGC32955","biotype":"protein_coding","ncbi_id":"340351","summary":null,"start":134986508,"end":135147963,"strand":1,"description":"ATP/GTP binding protein like 3 [Source:HGNC Symbol;Acc:HGNC:27981]"}, {"versioned_ensembl_gene_id":"ENSG00000101333.16","gene_symbol":"PLCB4","gene_name":"phospholipase C beta 4 [Source:HGNC Symbol;Acc:HGNC:9059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5332","summary":"The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of many extracellular signals in the retina. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2010]","start":9068763,"end":9481242,"strand":1,"description":"phospholipase C beta 4 [Source:HGNC Symbol;Acc:HGNC:9059]"}, {"versioned_ensembl_gene_id":"ENSG00000253155.1","gene_symbol":"AC008676.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157422439,"end":157422873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226130.1","gene_symbol":"AC013248.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14725729,"end":14729686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232504.4","gene_symbol":"ST3GAL5-AS1","gene_name":"ST3GAL5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51129]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928113","summary":null,"start":85889280,"end":85890980,"strand":1,"description":"ST3GAL5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51129]"}, {"versioned_ensembl_gene_id":"ENSG00000198261.3","gene_symbol":"OR5BB1P","gene_name":"olfactory receptor family 5 subfamily BB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15271]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81209","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59391354,"end":59392292,"strand":-1,"description":"olfactory receptor family 5 subfamily BB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15271]"}, {"versioned_ensembl_gene_id":"ENSG00000260863.1","gene_symbol":"CYP2C60P","gene_name":"cytochrome P450 family 2 subfamily C member 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:42410]","synonyms":"CYP2C8-de6b","biotype":"unprocessed_pseudogene","ncbi_id":"106480748","summary":null,"start":95009674,"end":95009812,"strand":1,"description":"cytochrome P450 family 2 subfamily C member 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:42410]"}, {"versioned_ensembl_gene_id":"ENSG00000228460.1","gene_symbol":"CYP2C59P","gene_name":"cytochrome P450 family 2 subfamily C member 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:42406]","synonyms":"CYP2C9-de2c3c","biotype":"unprocessed_pseudogene","ncbi_id":"100874505","summary":null,"start":95007126,"end":95007556,"strand":-1,"description":"cytochrome P450 family 2 subfamily C member 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:42406]"}, {"versioned_ensembl_gene_id":"ENSG00000234492.4","gene_symbol":"RPL34-AS1","gene_name":"RPL34 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26749]","synonyms":"RP11-462C24.1,FLJ37673","biotype":"lincRNA","ncbi_id":"285456","summary":null,"start":108538190,"end":108620460,"strand":-1,"description":"RPL34 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26749]"}, {"versioned_ensembl_gene_id":"ENSG00000255386.1","gene_symbol":"OR5BR1P","gene_name":"olfactory receptor family 5 subfamily BR member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15279]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81201","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59332757,"end":59334086,"strand":-1,"description":"olfactory receptor family 5 subfamily BR member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15279]"}, {"versioned_ensembl_gene_id":"ENSG00000250099.1","gene_symbol":"AC091893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24749374,"end":24749772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254704.3","gene_symbol":"AP002358.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59287339,"end":59289486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175567.8","gene_symbol":"UCP2","gene_name":"uncoupling protein 2 [Source:HGNC Symbol;Acc:HGNC:12518]","synonyms":"SLC25A8,BMIQ4","biotype":"protein_coding","ncbi_id":"7351","summary":"Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. This gene is expressed in many tissues, with the greatest expression in skeletal muscle. It is thought to play a role in nonshivering thermogenesis, obesity and diabetes. Chromosomal order is 5'-UCP3-UCP2-3'. [provided by RefSeq, Jul 2008]","start":73974667,"end":73983307,"strand":-1,"description":"uncoupling protein 2 [Source:HGNC Symbol;Acc:HGNC:12518]"}, {"versioned_ensembl_gene_id":"ENSG00000218089.1","gene_symbol":"DNAJA1P4","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728614","summary":null,"start":114349483,"end":114350648,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39340]"}, {"versioned_ensembl_gene_id":"ENSG00000267780.2","gene_symbol":"AC021594.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79792726,"end":79816529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278095.1","gene_symbol":"AC022509.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26273329,"end":26273900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198563.13","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"BAT1,UAP56,D6S81E","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31530219,"end":31542448,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000242293.1","gene_symbol":"RPS29P1","gene_name":"ribosomal protein S29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122449","summary":null,"start":69023150,"end":69023308,"strand":-1,"description":"ribosomal protein S29 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19783]"}, {"versioned_ensembl_gene_id":"ENSG00000176386.8","gene_symbol":"CDC26","gene_name":"cell division cycle 26 [Source:HGNC Symbol;Acc:HGNC:17839]","synonyms":"C9orf17,APC12,ANAPC12","biotype":"protein_coding","ncbi_id":"246184","summary":"The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc26, a component of cell cycle anaphase-promoting complex (APC). APC is composed of a group of highly conserved proteins and functions as a cell cycle-regulated ubiquitin-protein ligase. APC thus is responsible for the cell cycle regulated proteolysis of various proteins. [provided by RefSeq, Jul 2008]","start":113255835,"end":113275589,"strand":-1,"description":"cell division cycle 26 [Source:HGNC Symbol;Acc:HGNC:17839]"}, {"versioned_ensembl_gene_id":"ENSG00000206435.10","gene_symbol":"HLA-C","gene_name":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]","synonyms":"HLA-JY3,D6S204,PSORS1","biotype":"protein_coding","ncbi_id":"3107","summary":"HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":31262172,"end":31265564,"strand":-1,"description":"major histocompatibility complex, class I, C [Source:HGNC Symbol;Acc:HGNC:4933]"}, {"versioned_ensembl_gene_id":"ENSG00000136867.10","gene_symbol":"SLC31A2","gene_name":"solute carrier family 31 member 2 [Source:HGNC Symbol;Acc:HGNC:11017]","synonyms":"hCTR2,CTR2,COPT2","biotype":"protein_coding","ncbi_id":"1318","summary":null,"start":113150942,"end":113164137,"strand":1,"description":"solute carrier family 31 member 2 [Source:HGNC Symbol;Acc:HGNC:11017]"}, {"versioned_ensembl_gene_id":"ENSG00000280512.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195739964,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000075826.16","gene_symbol":"SEC31B","gene_name":"SEC31 homolog B, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:23197]","synonyms":"SEC31L2,SEC31B-1,DKFZP434M183","biotype":"protein_coding","ncbi_id":"25956","summary":"This gene encodes a protein of unknown function. The protein has moderate similarity to rat VAP1 protein which is an endosomal membrane-associated protein, containing a putative Ca2+/calmodulin-dependent kinase II phosphorylation site. [provided by RefSeq, Jul 2008]","start":100486642,"end":100519864,"strand":-1,"description":"SEC31 homolog B, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:23197]"}, {"versioned_ensembl_gene_id":"ENSG00000227489.1","gene_symbol":"AC006458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15066207,"end":15068651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224829.3","gene_symbol":"TOMM20P1","gene_name":"TOMM20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105369446","summary":null,"start":77313606,"end":77314032,"strand":1,"description":"TOMM20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50518]"}, {"versioned_ensembl_gene_id":"ENSG00000234670.1","gene_symbol":"OR6C64P","gene_name":"olfactory receptor family 6 subfamily C member 64 pseudogene [Source:HGNC Symbol;Acc:HGNC:31294]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403281","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55522593,"end":55523417,"strand":1,"description":"olfactory receptor family 6 subfamily C member 64 pseudogene [Source:HGNC Symbol;Acc:HGNC:31294]"}, {"versioned_ensembl_gene_id":"ENSG00000115368.9","gene_symbol":"WDR75","gene_name":"WD repeat domain 75 [Source:HGNC Symbol;Acc:HGNC:25725]","synonyms":"UTP17,NET16,FLJ12519","biotype":"protein_coding","ncbi_id":"84128","summary":null,"start":189441433,"end":189475565,"strand":1,"description":"WD repeat domain 75 [Source:HGNC Symbol;Acc:HGNC:25725]"}, {"versioned_ensembl_gene_id":"ENSG00000179695.2","gene_symbol":"OR6C2","gene_name":"olfactory receptor family 6 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:15436]","synonyms":"OR6C67","biotype":"protein_coding","ncbi_id":"341416","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55444069,"end":55453347,"strand":1,"description":"olfactory receptor family 6 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:15436]"}, {"versioned_ensembl_gene_id":"ENSG00000115525.17","gene_symbol":"ST3GAL5","gene_name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10872]","synonyms":"ST3GalV,SIATGM3S,SIAT9","biotype":"protein_coding","ncbi_id":"8869","summary":"Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":85837120,"end":85905199,"strand":-1,"description":"ST3 beta-galactoside alpha-2,3-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:10872]"}, {"versioned_ensembl_gene_id":"ENSG00000151366.12","gene_symbol":"NDUFC2","gene_name":"NADH:ubiquinone oxidoreductase subunit C2 [Source:HGNC Symbol;Acc:HGNC:7706]","synonyms":"HLC-1,B14.5b","biotype":"protein_coding","ncbi_id":"4718","summary":null,"start":78068304,"end":78080219,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit C2 [Source:HGNC Symbol;Acc:HGNC:7706]"}, {"versioned_ensembl_gene_id":"ENSG00000147100.10","gene_symbol":"SLC16A2","gene_name":"solute carrier family 16 member 2 [Source:HGNC Symbol;Acc:HGNC:10923]","synonyms":"XPCT,MRX22,MCT8,MCT7,DXS128,AHDS","biotype":"protein_coding","ncbi_id":"6567","summary":"This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012]","start":74421461,"end":74533917,"strand":1,"description":"solute carrier family 16 member 2 [Source:HGNC Symbol;Acc:HGNC:10923]"}, {"versioned_ensembl_gene_id":"ENSG00000169018.5","gene_symbol":"FEM1B","gene_name":"fem-1 homolog B [Source:HGNC Symbol;Acc:HGNC:3649]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10116","summary":"This gene encodes an ankyrin repeat protein that belongs to the death receptor-associated family of proteins and plays a role in mediating apoptosis. The encoded protein is also thought to function in the replication stress-induced checkpoint signaling pathway via interaction with checkpoint kinase 1. [provided by RefSeq, Aug 2013]","start":68277803,"end":68295865,"strand":1,"description":"fem-1 homolog B [Source:HGNC Symbol;Acc:HGNC:3649]"}, {"versioned_ensembl_gene_id":"ENSG00000224403.1","gene_symbol":"DPPA2P3","gene_name":"developmental pluripotency associated 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128023","summary":null,"start":193993331,"end":193993985,"strand":-1,"description":"developmental pluripotency associated 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44628]"}, {"versioned_ensembl_gene_id":"ENSG00000127452.8","gene_symbol":"FBXL12","gene_name":"F-box and leucine rich repeat protein 12 [Source:HGNC Symbol;Acc:HGNC:13611]","synonyms":"FLJ20188,Fbl12","biotype":"protein_coding","ncbi_id":"54850","summary":"Members of the F-box protein family, such as FBXL12, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":9810267,"end":9827816,"strand":-1,"description":"F-box and leucine rich repeat protein 12 [Source:HGNC Symbol;Acc:HGNC:13611]"}, {"versioned_ensembl_gene_id":"ENSG00000198851.9","gene_symbol":"CD3E","gene_name":"CD3e molecule [Source:HGNC Symbol;Acc:HGNC:1674]","synonyms":null,"biotype":"protein_coding","ncbi_id":"916","summary":"The protein encoded by this gene is the CD3-epsilon polypeptide, which together with CD3-gamma, -delta and -zeta, and the T-cell receptor alpha/beta and gamma/delta heterodimers, forms the T-cell receptor-CD3 complex. This complex plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. The genes encoding the epsilon, gamma and delta polypeptides are located in the same cluster on chromosome 11. The epsilon polypeptide plays an essential role in T-cell development. Defects in this gene cause immunodeficiency. This gene has also been linked to a susceptibility to type I diabetes in women. [provided by RefSeq, Jul 2008]","start":118304545,"end":118316175,"strand":1,"description":"CD3e molecule [Source:HGNC Symbol;Acc:HGNC:1674]"}, {"versioned_ensembl_gene_id":"ENSG00000237476.1","gene_symbol":"LINC01637","gene_name":"long intergenic non-protein coding RNA 1637 [Source:HGNC Symbol;Acc:HGNC:52424]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928891","summary":null,"start":20957092,"end":20964679,"strand":1,"description":"long intergenic non-protein coding RNA 1637 [Source:HGNC Symbol;Acc:HGNC:52424]"}, {"versioned_ensembl_gene_id":"ENSG00000164556.7","gene_symbol":"FAM183BP","gene_name":"family with sequence similarity 183 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:34511]","synonyms":"LOC340286,FAM183B","biotype":"processed_pseudogene","ncbi_id":"340286","summary":null,"start":38685346,"end":38687037,"strand":-1,"description":"family with sequence similarity 183 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:34511]"}, {"versioned_ensembl_gene_id":"ENSG00000227404.1","gene_symbol":"KRT8P20","gene_name":"keratin 8 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:33372]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441218","summary":null,"start":38655205,"end":38656613,"strand":1,"description":"keratin 8 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:33372]"}, {"versioned_ensembl_gene_id":"ENSG00000119673.14","gene_symbol":"ACOT2","gene_name":"acyl-CoA thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:18431]","synonyms":"ZAP128,Mte1","biotype":"protein_coding","ncbi_id":"10965","summary":"This gene encodes a member of the acyl-CoA thioesterase protein family, and is one of four acyl-CoA hydrolase genes located in a cluster on chromosome 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":73567620,"end":73575658,"strand":1,"description":"acyl-CoA thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:18431]"}, {"versioned_ensembl_gene_id":"ENSG00000165704.14","gene_symbol":"HPRT1","gene_name":"hypoxanthine phosphoribosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5157]","synonyms":"HPRT,HGPRT","biotype":"protein_coding","ncbi_id":"3251","summary":"The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009]","start":134460153,"end":134520513,"strand":1,"description":"hypoxanthine phosphoribosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:5157]"}, {"versioned_ensembl_gene_id":"ENSG00000129354.11","gene_symbol":"AP1M2","gene_name":"adaptor related protein complex 1 mu 2 subunit [Source:HGNC Symbol;Acc:HGNC:558]","synonyms":"mu2,HSMU1B,AP1-mu2","biotype":"protein_coding","ncbi_id":"10053","summary":"This gene encodes a subunit of the heterotetrameric adaptor-related protein comlex 1 (AP-1), which belongs to the adaptor complexes medium subunits family. This protein is capable of interacting with tyrosine-based sorting signals. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":10572671,"end":10587315,"strand":-1,"description":"adaptor related protein complex 1 mu 2 subunit [Source:HGNC Symbol;Acc:HGNC:558]"}, {"versioned_ensembl_gene_id":"ENSG00000261713.6","gene_symbol":"SSTR5-AS1","gene_name":"SSTR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26502]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"146336","summary":null,"start":1064093,"end":1078731,"strand":-1,"description":"SSTR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26502]"}, {"versioned_ensembl_gene_id":"ENSG00000175967.3","gene_symbol":"FO393415.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113904138,"end":113921642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118985.15","gene_symbol":"ELL2","gene_name":"elongation factor for RNA polymerase II 2 [Source:HGNC Symbol;Acc:HGNC:17064]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22936","summary":null,"start":95885098,"end":95962071,"strand":-1,"description":"elongation factor for RNA polymerase II 2 [Source:HGNC Symbol;Acc:HGNC:17064]"}, {"versioned_ensembl_gene_id":"ENSG00000278914.1","gene_symbol":"AP003355.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":98391401,"end":98391514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079432.7","gene_symbol":"CIC","gene_name":"capicua transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:14214]","synonyms":"KIAA0306","biotype":"protein_coding","ncbi_id":"23152","summary":"The protein encoded by this gene is an ortholog of the Drosophila melanogaster capicua gene, and is a member of the high mobility group (HMG)-box superfamily of transcriptional repressors. This protein contains a conserved HMG domain that is involved in DNA binding and nuclear localization, and a conserved C-terminus. Studies suggest that the N-terminal region of this protein interacts with Atxn1 (GeneID:6310), to form a transcription repressor complex, and in vitro studies suggest that polyglutamine-expansion of ATXN1 may alter the repressor activity of this complex. Mutations in this gene have been associated with olidogdendrogliomas (PMID:21817013). In addition, translocation events resulting in gene fusions of this gene with both DUX4 (GeneID:100288687) and FOXO4 (GeneID:4303) have been associated with round cell sarcomas. There are multiple pseudogenes of this gene found on chromosomes 1, 4, 6, 7, 16, 20, and the Y chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]","start":42268537,"end":42295797,"strand":1,"description":"capicua transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:14214]"}, {"versioned_ensembl_gene_id":"ENSG00000203772.7","gene_symbol":"SPRN","gene_name":"shadow of prion protein [Source:HGNC Symbol;Acc:HGNC:16871]","synonyms":"Sprn,Shadoo,FLJ41197,bA108K14.1","biotype":"protein_coding","ncbi_id":"503542","summary":null,"start":133420666,"end":133424572,"strand":-1,"description":"shadow of prion protein [Source:HGNC Symbol;Acc:HGNC:16871]"}, {"versioned_ensembl_gene_id":"ENSG00000233845.1","gene_symbol":"AC093732.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47035279,"end":47040524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274895.1","gene_symbol":"AC011700.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":213983793,"end":213986419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259923.1","gene_symbol":"AC026461.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":56648881,"end":56652636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272167.2","gene_symbol":"AL606537.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":214028891,"end":214030901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204262.11","gene_symbol":"COL5A2","gene_name":"collagen type V alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2210]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1290","summary":"This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. [provided by RefSeq, Jul 2008]","start":189031896,"end":189179879,"strand":-1,"description":"collagen type V alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2210]"}, {"versioned_ensembl_gene_id":"ENSG00000205361.8","gene_symbol":"MT1DP","gene_name":"metallothionein 1D, pseudogene [Source:HGNC Symbol;Acc:HGNC:7396]","synonyms":"MTM","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"326343","summary":null,"start":56643705,"end":56644786,"strand":1,"description":"metallothionein 1D, pseudogene [Source:HGNC Symbol;Acc:HGNC:7396]"}, {"versioned_ensembl_gene_id":"ENSG00000238196.5","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32261849,"end":32271406,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000228646.3","gene_symbol":"RPL31P13","gene_name":"ribosomal protein L31 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270983","summary":null,"start":213428708,"end":213429077,"strand":-1,"description":"ribosomal protein L31 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35598]"}, {"versioned_ensembl_gene_id":"ENSG00000232299.1","gene_symbol":"AL357514.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112476538,"end":112481636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265203.1","gene_symbol":"RBP3","gene_name":"retinol binding protein 3 [Source:HGNC Symbol;Acc:HGNC:9921]","synonyms":"RP66,D10S66,D10S65,D10S64","biotype":"protein_coding","ncbi_id":"5949","summary":"Interphotoreceptor retinol-binding protein is a large glycoprotein known to bind retinoids and found primarily in the interphotoreceptor matrix of the retina between the retinal pigment epithelium and the photoreceptor cells. It is thought to transport retinoids between the retinal pigment epithelium and the photoreceptors, a critical role in the visual process.The human IRBP gene is approximately 9.5 kbp in length and consists of four exons separated by three introns. The introns are 1.6-1.9 kbp long. The gene is transcribed by photoreceptor and retinoblastoma cells into an approximately 4.3-kilobase mRNA that is translated and processed into a glycosylated protein of 135,000 Da. The amino acid sequence of human IRBP can be divided into four contiguous homology domains with 33-38% identity, suggesting a series of gene duplication events. In the gene, the boundaries of these domains are not defined by exon-intron junctions, as might have been expected. The first three homology domains and part of the fourth are all encoded by the first large exon, which is 3,180 base pairs long. The remainder of the fourth domain is encoded in the last three exons, which are 191, 143, and approximately 740 base pairs long, respectively. [provided by RefSeq, Jul 2008]","start":47348371,"end":47357875,"strand":1,"description":"retinol binding protein 3 [Source:HGNC Symbol;Acc:HGNC:9921]"}, {"versioned_ensembl_gene_id":"ENSG00000004897.11","gene_symbol":"CDC27","gene_name":"cell division cycle 27 [Source:HGNC Symbol;Acc:HGNC:1728]","synonyms":"NUC2,D17S978E,D0S1430E,APC3,ANAPC3","biotype":"protein_coding","ncbi_id":"996","summary":"The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae protein Cdc27, and the gene product of Schizosaccharomyces pombe nuc 2. This protein is a component of the anaphase-promoting complex (APC), which is composed of eight protein subunits and is highly conserved in eukaryotic cells. This complex catalyzes the formation of cyclin B-ubiquitin conjugate, which is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. The protein encoded by this gene and three other members of the APC complex contain tetratricopeptide (TPR) repeats, which are important for protein-protein interactions. This protein was shown to interact with mitotic checkpoint proteins including Mad2, p55CDC and BUBR1, and it may thus be involved in controlling the timing of mitosis. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2, 22 and Y. [provided by RefSeq, May 2014]","start":47117703,"end":47189422,"strand":-1,"description":"cell division cycle 27 [Source:HGNC Symbol;Acc:HGNC:1728]"}, {"versioned_ensembl_gene_id":"ENSG00000130396.20","gene_symbol":"AFDN","gene_name":"afadin, adherens junction formation factor [Source:HGNC Symbol;Acc:HGNC:7137]","synonyms":"AF-6,MLLT4,AF6","biotype":"protein_coding","ncbi_id":"4301","summary":"This gene encodes a multi-domain protein involved in signaling and organization of cell junctions during embryogenesis. It has also been identified as the fusion partner of acute lymphoblastic leukemia (ALL-1) gene, involved in acute myeloid leukemias with t(6;11)(q27;q23) translocation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, however, not all have been fully characterized.[provided by RefSeq, May 2011]","start":167826922,"end":167972023,"strand":1,"description":"afadin, adherens junction formation factor [Source:HGNC Symbol;Acc:HGNC:7137]"}, {"versioned_ensembl_gene_id":"ENSG00000205329.2","gene_symbol":"OR6C3","gene_name":"olfactory receptor family 6 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:15437]","synonyms":"OST709","biotype":"protein_coding","ncbi_id":"254786","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55330043,"end":55332687,"strand":1,"description":"olfactory receptor family 6 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:15437]"}, {"versioned_ensembl_gene_id":"ENSG00000225730.1","gene_symbol":"AL096772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46903471,"end":46909078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230994.1","gene_symbol":"FGFR3P1","gene_name":"fibroblast growth factor receptor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21664]","synonyms":"FGFR3P,D84394.2,FGFR6","biotype":"processed_pseudogene","ncbi_id":"100462812","summary":null,"start":31377419,"end":31378019,"strand":1,"description":"fibroblast growth factor receptor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21664]"}, {"versioned_ensembl_gene_id":"ENSG00000240042.2","gene_symbol":"AC098789.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268606,"end":54269646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276542.1","gene_symbol":"AC097478.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89748283,"end":89749154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135077.8","gene_symbol":"HAVCR2","gene_name":"hepatitis A virus cellular receptor 2 [Source:HGNC Symbol;Acc:HGNC:18437]","synonyms":"TIMD3,TIM3,Tim-3,FLJ14428,CD366","biotype":"protein_coding","ncbi_id":"84868","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily, and TIM family of proteins. CD4-positive T helper lymphocytes can be divided into types 1 (Th1) and 2 (Th2) on the basis of their cytokine secretion patterns. Th1 cells are involved in cell-mediated immunity to intracellular pathogens and delayed-type hypersensitivity reactions, whereas, Th2 cells are involved in the control of extracellular helminthic infections and the promotion of atopic and allergic diseases. This protein is a Th1-specific cell surface protein that regulates macrophage activation, and inhibits Th1-mediated auto- and alloimmune responses, and promotes immunological tolerance. [provided by RefSeq, Sep 2011]","start":157085832,"end":157142869,"strand":-1,"description":"hepatitis A virus cellular receptor 2 [Source:HGNC Symbol;Acc:HGNC:18437]"}, {"versioned_ensembl_gene_id":"ENSG00000269281.2","gene_symbol":"AC244505.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52770809,"end":52771080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187754.8","gene_symbol":"SSX7","gene_name":"SSX family member 7 [Source:HGNC Symbol;Acc:HGNC:19653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"280658","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This gene appears not to be involved in this type of chromosome translocation. [provided by RefSeq, Jul 2008]","start":52644090,"end":52654900,"strand":-1,"description":"SSX family member 7 [Source:HGNC Symbol;Acc:HGNC:19653]"}, {"versioned_ensembl_gene_id":"ENSG00000250712.1","gene_symbol":"AC106872.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165010459,"end":165011851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115590.13","gene_symbol":"IL1R2","gene_name":"interleukin 1 receptor type 2 [Source:HGNC Symbol;Acc:HGNC:5994]","synonyms":"IL1RB,CD121b","biotype":"protein_coding","ncbi_id":"7850","summary":"The protein encoded by this gene is a cytokine receptor that belongs to the interleukin 1 receptor family. This protein binds interleukin alpha (IL1A), interleukin beta (IL1B), and interleukin 1 receptor, type I(IL1R1/IL1RA), and acts as a decoy receptor that inhibits the activity of its ligands. Interleukin 4 (IL4) is reported to antagonize the activity of interleukin 1 by inducing the expression and release of this cytokine. This gene and three other genes form a cytokine receptor gene cluster on chromosome 2q12. Alternative splicing results in multiple transcript variants and protein isoforms. Alternative splicing produces both membrane-bound and soluble proteins. A soluble protein is also produced by proteolytic cleavage. [provided by RefSeq, May 2012]","start":101991844,"end":102028544,"strand":1,"description":"interleukin 1 receptor type 2 [Source:HGNC Symbol;Acc:HGNC:5994]"}, {"versioned_ensembl_gene_id":"ENSG00000169213.6","gene_symbol":"RAB3B","gene_name":"RAB3B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9778]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5865","summary":null,"start":51907956,"end":51990764,"strand":-1,"description":"RAB3B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9778]"}, {"versioned_ensembl_gene_id":"ENSG00000258667.1","gene_symbol":"HIF1A-AS2","gene_name":"HIF1A antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43015]","synonyms":"aHIF,3'aHIF-1A","biotype":"lincRNA","ncbi_id":"100750247","summary":null,"start":61715558,"end":61751097,"strand":-1,"description":"HIF1A antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43015]"}, {"versioned_ensembl_gene_id":"ENSG00000117069.14","gene_symbol":"ST6GALNAC5","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:19342]","synonyms":"ST6GalNAcV,SIAT7E,MGC3184","biotype":"protein_coding","ncbi_id":"81849","summary":"The protein encoded by this gene is a Golgi type II transmembrane glycosyltransferase. The encoded protein catalyzes the transfer of sialic acid to cell surface proteins to modulate cell-cell interactions. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":76867441,"end":77065711,"strand":1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:19342]"}, {"versioned_ensembl_gene_id":"ENSG00000232729.7","gene_symbol":"AC211433.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":74688939,"end":74729001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262648.1","gene_symbol":"PHBP15","gene_name":"prohibitin pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39294]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873752","summary":null,"start":74741457,"end":74742121,"strand":-1,"description":"prohibitin pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39294]"}, {"versioned_ensembl_gene_id":"ENSG00000137642.12","gene_symbol":"SORL1","gene_name":"sortilin related receptor 1 [Source:HGNC Symbol;Acc:HGNC:11185]","synonyms":"SorLA-1,SorLA,LRP9,LR11,gp250,C11orf32","biotype":"protein_coding","ncbi_id":"6653","summary":"This gene encodes a mosaic protein that belongs to at least two families: the vacuolar protein sorting 10 (VPS10) domain-containing receptor family, and the low density lipoprotein receptor (LDLR) family. The encoded protein also contains fibronectin type III repeats and an epidermal growth factor repeat. The encoded preproprotein is proteolytically processed to generate the mature receptor, which likely plays roles in endocytosis and sorting. Mutations in this gene may be associated with Alzheimer's disease. [provided by RefSeq, Feb 2016]","start":121452203,"end":121633693,"strand":1,"description":"sortilin related receptor 1 [Source:HGNC Symbol;Acc:HGNC:11185]"}, {"versioned_ensembl_gene_id":"ENSG00000076201.14","gene_symbol":"PTPN23","gene_name":"protein tyrosine phosphatase, non-receptor type 23 [Source:HGNC Symbol;Acc:HGNC:14406]","synonyms":"KIAA1471,HD-PTP,DKFZP564F0923","biotype":"protein_coding","ncbi_id":"25930","summary":"This gene encodes a member of the non-receptor type protein-tyrosine phosphatase family. The encoded protein may be involved in the regulation of small nuclear ribonucleo protein assembly and pre-mRNA splicing by modifying the survival motor neuron (SMN) complex. The encoded protein additionally plays a role in ciliogenesis and is part of endosomal sorting complex required for transport (ESCRT) pathways. This gene may serve a tumor suppressor function. [provided by RefSeq, Jul 2016]","start":47381011,"end":47413441,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 23 [Source:HGNC Symbol;Acc:HGNC:14406]"}, {"versioned_ensembl_gene_id":"ENSG00000237348.1","gene_symbol":"CR759798.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":33003767,"end":33004281,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184210.5","gene_symbol":"DGAT2L6","gene_name":"diacylglycerol O-acyltransferase 2 like 6 [Source:HGNC Symbol;Acc:HGNC:23250]","synonyms":"FLJ25989,DC3","biotype":"protein_coding","ncbi_id":"347516","summary":"This gene is a member of the diacylglycerol acyltransferase 2 family. The encoded protein is a putative acyltransferase and is most likely involved in the synthesis of di- or triacylglycerol, however its substrate specificity is currently unknown. [provided by RefSeq, Feb 2015]","start":70177483,"end":70205545,"strand":1,"description":"diacylglycerol O-acyltransferase 2 like 6 [Source:HGNC Symbol;Acc:HGNC:23250]"}, {"versioned_ensembl_gene_id":"ENSG00000259572.5","gene_symbol":"LINC01491","gene_name":"long intergenic non-protein coding RNA 1491 [Source:HGNC Symbol;Acc:HGNC:51148]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928442","summary":null,"start":47803384,"end":47846236,"strand":-1,"description":"long intergenic non-protein coding RNA 1491 [Source:HGNC Symbol;Acc:HGNC:51148]"}, {"versioned_ensembl_gene_id":"ENSG00000221891.2","gene_symbol":"FAM218BP","gene_name":"family with sequence similarity 218 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101059914","summary":null,"start":164929494,"end":164929951,"strand":-1,"description":"family with sequence similarity 218 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:43779]"}, {"versioned_ensembl_gene_id":"ENSG00000255534.1","gene_symbol":"OR4A43P","gene_name":"olfactory receptor family 4 subfamily A member 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:31262]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390117","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48526064,"end":48526971,"strand":1,"description":"olfactory receptor family 4 subfamily A member 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:31262]"}, {"versioned_ensembl_gene_id":"ENSG00000231643.4","gene_symbol":"Z70280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101191115,"end":101191409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272896.1","gene_symbol":"AL355987.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136791379,"end":136800595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229181.1","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"processed_transcript","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29444942,"end":29450170,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000230754.1","gene_symbol":"CR936918.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29268503,"end":29269462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183527.11","gene_symbol":"PSMG1","gene_name":"proteasome assembly chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3043]","synonyms":"PAC1,LRPC21,DSCR2,c21-LRP","biotype":"protein_coding","ncbi_id":"8624","summary":null,"start":39174769,"end":39183851,"strand":-1,"description":"proteasome assembly chaperone 1 [Source:HGNC Symbol;Acc:HGNC:3043]"}, {"versioned_ensembl_gene_id":"ENSG00000225550.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"hs6M1-6,dJ80I19.4,OR6-8","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173336,"end":29174607,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000140945.16","gene_symbol":"CDH13","gene_name":"cadherin 13 [Source:HGNC Symbol;Acc:HGNC:1753]","synonyms":"CDHH","biotype":"protein_coding","ncbi_id":"1012","summary":"This gene encodes a member of the cadherin superfamily. The encoded protein is localized to the surface of the cell membrane and is anchored by a GPI moiety, rather than by a transmembrane domain. The protein lacks the cytoplasmic domain characteristic of other cadherins, and so is not thought to be a cell-cell adhesion glycoprotein. This protein acts as a negative regulator of axon growth during neural differentiation. It also protects vascular endothelial cells from apoptosis due to oxidative stress, and is associated with resistance to atherosclerosis. The gene is hypermethylated in many types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2011]","start":82626803,"end":83800640,"strand":1,"description":"cadherin 13 [Source:HGNC Symbol;Acc:HGNC:1753]"}, {"versioned_ensembl_gene_id":"ENSG00000241324.1","gene_symbol":"AC004930.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124337380,"end":124349860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241344.1","gene_symbol":"RPL21P47","gene_name":"ribosomal protein L21 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271164","summary":null,"start":62248294,"end":62248770,"strand":1,"description":"ribosomal protein L21 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36711]"}, {"versioned_ensembl_gene_id":"ENSG00000278358.1","gene_symbol":"BX510359.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52480836,"end":52481131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224955.1","gene_symbol":"KCTD10P1","gene_name":"potassium channel tetramerization domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49807]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422230","summary":null,"start":28598668,"end":28599292,"strand":-1,"description":"potassium channel tetramerization domain containing 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49807]"}, {"versioned_ensembl_gene_id":"ENSG00000255521.1","gene_symbol":"AL356215.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35132655,"end":35138032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161850.2","gene_symbol":"KRT82","gene_name":"keratin 82 [Source:HGNC Symbol;Acc:HGNC:6459]","synonyms":"KRTHB2,Hb-2","biotype":"protein_coding","ncbi_id":"3888","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this keratin appears to be a hair cuticle-specific keratin. [provided by RefSeq, Jul 2008]","start":52393931,"end":52406355,"strand":-1,"description":"keratin 82 [Source:HGNC Symbol;Acc:HGNC:6459]"}, {"versioned_ensembl_gene_id":"ENSG00000146281.5","gene_symbol":"PM20D2","gene_name":"peptidase M20 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21408]","synonyms":"bA63L7.3,ACY1L2","biotype":"protein_coding","ncbi_id":"135293","summary":null,"start":89146050,"end":89165565,"strand":1,"description":"peptidase M20 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21408]"}, {"versioned_ensembl_gene_id":"ENSG00000182965.6","gene_symbol":"NPM1P14","gene_name":"nucleophosmin 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:7916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10833","summary":null,"start":112520488,"end":112521670,"strand":1,"description":"nucleophosmin 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:7916]"}, {"versioned_ensembl_gene_id":"ENSG00000232479.2","gene_symbol":"AC010900.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202924609,"end":202925904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230851.1","gene_symbol":"AP006294.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3591277,"end":3591615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177098.8","gene_symbol":"SCN4B","gene_name":"sodium voltage-gated channel beta subunit 4 [Source:HGNC Symbol;Acc:HGNC:10592]","synonyms":"LQT10","biotype":"protein_coding","ncbi_id":"6330","summary":"The protein encoded by this gene is one of several sodium channel beta subunits. These subunits interact with voltage-gated alpha subunits to change sodium channel kinetics. The encoded transmembrane protein forms interchain disulfide bonds with SCN2A. Defects in this gene are a cause of long QT syndrome type 10 (LQT10). Three protein-coding and one non-coding transcript variant have been found for this gene.[provided by RefSeq, Mar 2009]","start":118133377,"end":118152888,"strand":-1,"description":"sodium voltage-gated channel beta subunit 4 [Source:HGNC Symbol;Acc:HGNC:10592]"}, {"versioned_ensembl_gene_id":"ENSG00000151148.13","gene_symbol":"UBE3B","gene_name":"ubiquitin protein ligase E3B [Source:HGNC Symbol;Acc:HGNC:13478]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89910","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: E1 ubiquitin-activating enzymes, E2 ubiquitin-conjugating enzymes, and E3 ubiquitin-protein ligases. This gene encodes a member of the E3 ubiquitin-conjugating enzyme family which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme and transfers the ubiquitin to the targeted substrates. A HECT (homology to E6-AP C-terminus) domain in the C-terminus of the longer isoform of this protein is the catalytic site of ubiquitin transfer and forms a complex with E2 conjugases. Shorter isoforms of this protein which lack the C-terminal HECT domain are therefore unlikely to bind E2 enzymes. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2012]","start":109477402,"end":109536705,"strand":1,"description":"ubiquitin protein ligase E3B [Source:HGNC Symbol;Acc:HGNC:13478]"}, {"versioned_ensembl_gene_id":"ENSG00000261058.1","gene_symbol":"AC099508.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75119558,"end":75144200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282564.1","gene_symbol":"AL133516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":230426491,"end":230436822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254706.2","gene_symbol":"AL512785.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":162365407,"end":162383531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271653.1","gene_symbol":"AC097359.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37216779,"end":37217988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250422.1","gene_symbol":"AC117529.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45557919,"end":45559986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170605.6","gene_symbol":"OR9K2","gene_name":"olfactory receptor family 9 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15339]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441639","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55126406,"end":55132750,"strand":1,"description":"olfactory receptor family 9 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:15339]"}, {"versioned_ensembl_gene_id":"ENSG00000231449.1","gene_symbol":"AC097359.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37196204,"end":37196666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131409.12","gene_symbol":"LRRC4B","gene_name":"leucine rich repeat containing 4B [Source:HGNC Symbol;Acc:HGNC:25042]","synonyms":"LRIG4,HSM,DKFZp761A179","biotype":"protein_coding","ncbi_id":"94030","summary":null,"start":50516892,"end":50568045,"strand":-1,"description":"leucine rich repeat containing 4B [Source:HGNC Symbol;Acc:HGNC:25042]"}, {"versioned_ensembl_gene_id":"ENSG00000261744.1","gene_symbol":"AC116552.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88512960,"end":88531053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231508.1","gene_symbol":"RPL34P20","gene_name":"ribosomal protein L34 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35535]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271308","summary":null,"start":97393197,"end":97393547,"strand":-1,"description":"ribosomal protein L34 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35535]"}, {"versioned_ensembl_gene_id":"ENSG00000270512.1","gene_symbol":"AC005377.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140282465,"end":140282920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259819.1","gene_symbol":"AC018767.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8369864,"end":8376276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234767.1","gene_symbol":"LINC01052","gene_name":"long intergenic non-protein coding RNA 1052 [Source:HGNC Symbol;Acc:HGNC:49046]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370242","summary":null,"start":65866174,"end":65878219,"strand":1,"description":"long intergenic non-protein coding RNA 1052 [Source:HGNC Symbol;Acc:HGNC:49046]"}, {"versioned_ensembl_gene_id":"ENSG00000214266.2","gene_symbol":"STARP1","gene_name":"steroidogenic acute regulatory protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11360]","synonyms":"STARD1P1","biotype":"processed_pseudogene","ncbi_id":"6771","summary":null,"start":65309855,"end":65310953,"strand":-1,"description":"steroidogenic acute regulatory protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11360]"}, {"versioned_ensembl_gene_id":"ENSG00000181013.3","gene_symbol":"C17orf47","gene_name":"chromosome 17 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26844]","synonyms":"FLJ40121","biotype":"protein_coding","ncbi_id":"284083","summary":null,"start":58541587,"end":58544368,"strand":-1,"description":"chromosome 17 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:26844]"}, {"versioned_ensembl_gene_id":"ENSG00000072786.12","gene_symbol":"STK10","gene_name":"serine/threonine kinase 10 [Source:HGNC Symbol;Acc:HGNC:11388]","synonyms":"PRO2729,LOK","biotype":"protein_coding","ncbi_id":"6793","summary":"This gene encodes a member of the Ste20 family of serine/threonine protein kinases, and is similar to several known polo-like kinase kinases. The protein can associate with and phosphorylate polo-like kinase 1, and overexpression of a kinase-dead version of the protein interferes with normal cell cycle progression. The kinase can also negatively regulate interleukin 2 expression in T-cells via the mitogen activated protein kinase kinase 1 pathway. [provided by RefSeq, Jul 2008]","start":172042073,"end":172188386,"strand":-1,"description":"serine/threonine kinase 10 [Source:HGNC Symbol;Acc:HGNC:11388]"}, {"versioned_ensembl_gene_id":"ENSG00000205090.8","gene_symbol":"TMEM240","gene_name":"transmembrane protein 240 [Source:HGNC Symbol;Acc:HGNC:25186]","synonyms":"SCA21,C1orf70","biotype":"protein_coding","ncbi_id":"339453","summary":"This gene encodes a transmembrane-domain containing protein found in the brain and cerebellum. Mutations in this gene result in spinocerebellar ataxia 21. [provided by RefSeq, Dec 2014]","start":1535174,"end":1540453,"strand":-1,"description":"transmembrane protein 240 [Source:HGNC Symbol;Acc:HGNC:25186]"}, {"versioned_ensembl_gene_id":"ENSG00000275793.1","gene_symbol":"RIMBP3","gene_name":"RIMS binding protein 3 [Source:HGNC Symbol;Acc:HGNC:29344]","synonyms":"KIAA1666,RIMBP3A,RIMBP3.1","biotype":"protein_coding","ncbi_id":"85376","summary":null,"start":18605815,"end":18611919,"strand":-1,"description":"RIMS binding protein 3 [Source:HGNC Symbol;Acc:HGNC:29344]"}, {"versioned_ensembl_gene_id":"ENSG00000263263.1","gene_symbol":"KRTAP9-6","gene_name":"keratin associated protein 9-6 [Source:HGNC Symbol;Acc:HGNC:18914]","synonyms":"KRTAP9L2,KAP9.6","biotype":"protein_coding","ncbi_id":"100507608","summary":null,"start":41253969,"end":41255271,"strand":1,"description":"keratin associated protein 9-6 [Source:HGNC Symbol;Acc:HGNC:18914]"}, {"versioned_ensembl_gene_id":"ENSG00000142484.6","gene_symbol":"TM4SF5","gene_name":"transmembrane 4 L six family member 5 [Source:HGNC Symbol;Acc:HGNC:11857]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9032","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and is highly similar in sequence and structure to transmembrane 4 superfamily member 1. It may play a role in cell proliferation, and overexpression of this protein may be associated with the uncontrolled growth of tumour cells. [provided by RefSeq, Jul 2008]","start":4771884,"end":4783213,"strand":1,"description":"transmembrane 4 L six family member 5 [Source:HGNC Symbol;Acc:HGNC:11857]"}, {"versioned_ensembl_gene_id":"ENSG00000233772.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33227453,"end":33232908,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000280482.1","gene_symbol":"AC233280.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176231.2","gene_symbol":"OR10H4","gene_name":"olfactory receptor family 10 subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:15388]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126541","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15944299,"end":15950350,"strand":1,"description":"olfactory receptor family 10 subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:15388]"}, {"versioned_ensembl_gene_id":"ENSG00000121775.17","gene_symbol":"TMEM39B","gene_name":"transmembrane protein 39B [Source:HGNC Symbol;Acc:HGNC:25510]","synonyms":"FLJ10315","biotype":"protein_coding","ncbi_id":"55116","summary":null,"start":32072031,"end":32102866,"strand":1,"description":"transmembrane protein 39B [Source:HGNC Symbol;Acc:HGNC:25510]"}, {"versioned_ensembl_gene_id":"ENSG00000203325.3","gene_symbol":"AL445248.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32052291,"end":32073474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248702.1","gene_symbol":"AC005921.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50797366,"end":50797651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254691.1","gene_symbol":"AP002812.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77850604,"end":77851511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186417.13","gene_symbol":"GLDN","gene_name":"gliomedin [Source:HGNC Symbol;Acc:HGNC:29514]","synonyms":"UNC-112,CRG-L2,colmedin,COLM,CLOM","biotype":"protein_coding","ncbi_id":"342035","summary":"This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]","start":51341629,"end":51408013,"strand":1,"description":"gliomedin [Source:HGNC Symbol;Acc:HGNC:29514]"}, {"versioned_ensembl_gene_id":"ENSG00000228853.1","gene_symbol":"NEGR1-IT1","gene_name":"NEGR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41432]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100852409","summary":null,"start":71794232,"end":71837012,"strand":-1,"description":"NEGR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41432]"}, {"versioned_ensembl_gene_id":"ENSG00000255627.1","gene_symbol":"AC092862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22008348,"end":22008880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184991.2","gene_symbol":"TTTY13","gene_name":"testis-specific transcript, Y-linked 13 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18494]","synonyms":"TTY13,NCRNA00136","biotype":"lincRNA","ncbi_id":"83868","summary":null,"start":21583600,"end":21594666,"strand":-1,"description":"testis-specific transcript, Y-linked 13 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18494]"}, {"versioned_ensembl_gene_id":"ENSG00000231985.1","gene_symbol":"AL354949.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71570956,"end":71573558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279621.1","gene_symbol":"AC020978.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68199841,"end":68200981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254443.1","gene_symbol":"AC068733.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6362799,"end":6365267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269933.1","gene_symbol":"AL031429.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71005854,"end":71006502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221571.3","gene_symbol":"RNU6ATAC35P","gene_name":"RNA, U6atac small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46934]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106481171","summary":null,"start":220825620,"end":220826063,"strand":1,"description":"RNA, U6atac small nuclear 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:46934]"}, {"versioned_ensembl_gene_id":"ENSG00000235782.1","gene_symbol":"AL031429.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70947379,"end":70951493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240785.2","gene_symbol":"RPL36AP21","gene_name":"ribosomal protein L36a pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37041]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271332","summary":null,"start":18049232,"end":18049872,"strand":1,"description":"ribosomal protein L36a pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37041]"}, {"versioned_ensembl_gene_id":"ENSG00000018699.11","gene_symbol":"TTC27","gene_name":"tetratricopeptide repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:25986]","synonyms":"FLJ20272","biotype":"protein_coding","ncbi_id":"55622","summary":null,"start":32628032,"end":32821051,"strand":1,"description":"tetratricopeptide repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:25986]"}, {"versioned_ensembl_gene_id":"ENSG00000251348.1","gene_symbol":"HSPD1P11","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35142]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100359396","summary":null,"start":95768999,"end":95770700,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35142]"}, {"versioned_ensembl_gene_id":"ENSG00000172362.3","gene_symbol":"OR5B12","gene_name":"olfactory receptor family 5 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15432]","synonyms":"OST743,OR5B16,OR5B12P","biotype":"protein_coding","ncbi_id":"390191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58439077,"end":58442758,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 12 [Source:HGNC Symbol;Acc:HGNC:15432]"}, {"versioned_ensembl_gene_id":"ENSG00000233139.1","gene_symbol":"AC244636.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48153868,"end":48155941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270794.1","gene_symbol":"AC005185.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30209423,"end":30210209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280789.1","gene_symbol":"PAGR1","gene_name":"PAXIP1 associated glutamate rich protein 1 [Source:HGNC Symbol;Acc:HGNC:28707]","synonyms":"PA1,MGC4606,GAS,C16orf53","biotype":"protein_coding","ncbi_id":"79447","summary":"C16ORF53 (PA1) is a component of a Set1-like multiprotein histone methyltransferase complex (Cho et al., 2007 [PubMed 17500065]).[supplied by OMIM, May 2008]","start":29815952,"end":29820117,"strand":1,"description":"PAXIP1 associated glutamate rich protein 1 [Source:HGNC Symbol;Acc:HGNC:28707]"}, {"versioned_ensembl_gene_id":"ENSG00000229425.2","gene_symbol":"AJ009632.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15370500,"end":15627342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236404.8","gene_symbol":"VLDLR-AS1","gene_name":"VLDLR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49621]","synonyms":"lincRNA-VLDLR","biotype":"antisense_RNA","ncbi_id":"401491","summary":null,"start":2422702,"end":2643359,"strand":-1,"description":"VLDLR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49621]"}, {"versioned_ensembl_gene_id":"ENSG00000224524.1","gene_symbol":"CYCSP42","gene_name":"cytochrome c, somatic pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:2581]","synonyms":"CYC1LP5","biotype":"processed_pseudogene","ncbi_id":"343727","summary":null,"start":15490530,"end":15490767,"strand":-1,"description":"cytochrome c, somatic pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:2581]"}, {"versioned_ensembl_gene_id":"ENSG00000224514.2","gene_symbol":"LINC00620","gene_name":"long intergenic non-protein coding RNA 620 [Source:HGNC Symbol;Acc:HGNC:44223]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285375","summary":null,"start":13650696,"end":13746637,"strand":1,"description":"long intergenic non-protein coding RNA 620 [Source:HGNC Symbol;Acc:HGNC:44223]"}, {"versioned_ensembl_gene_id":"ENSG00000115129.13","gene_symbol":"TP53I3","gene_name":"tumor protein p53 inducible protein 3 [Source:HGNC Symbol;Acc:HGNC:19373]","synonyms":"PIG3","biotype":"protein_coding","ncbi_id":"9540","summary":"The protein encoded by this gene is similar to oxidoreductases, which are enzymes involved in cellular responses to oxidative stresses and irradiation. This gene is induced by the tumor suppressor p53 and is thought to be involved in p53-mediated cell death. It contains a p53 consensus binding site in its promoter region and a downstream pentanucleotide microsatellite sequence. P53 has been shown to transcriptionally activate this gene by interacting with the downstream pentanucleotide microsatellite sequence. The microsatellite is polymorphic, with a varying number of pentanucleotide repeats directly correlated with the extent of transcriptional activation by p53. It has been suggested that the microsatellite polymorphism may be associated with differential susceptibility to cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":24077433,"end":24085861,"strand":-1,"description":"tumor protein p53 inducible protein 3 [Source:HGNC Symbol;Acc:HGNC:19373]"}, {"versioned_ensembl_gene_id":"ENSG00000171469.10","gene_symbol":"ZNF561","gene_name":"zinc finger protein 561 [Source:HGNC Symbol;Acc:HGNC:28684]","synonyms":"MGC45408","biotype":"protein_coding","ncbi_id":"93134","summary":null,"start":9604680,"end":9621399,"strand":-1,"description":"zinc finger protein 561 [Source:HGNC Symbol;Acc:HGNC:28684]"}, {"versioned_ensembl_gene_id":"ENSG00000227393.1","gene_symbol":"AL031575.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29369001,"end":29369845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226436.1","gene_symbol":"AC002367.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28659065,"end":28659469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134259.3","gene_symbol":"NGF","gene_name":"nerve growth factor [Source:HGNC Symbol;Acc:HGNC:7808]","synonyms":"NGFB","biotype":"protein_coding","ncbi_id":"4803","summary":"This gene is a member of the NGF-beta family and encodes a secreted protein which homodimerizes and is incorporated into a larger complex. This protein has nerve growth stimulating activity and the complex is involved in the regulation of growth and the differentiation of sympathetic and certain sensory neurons. Mutations in this gene have been associated with hereditary sensory and autonomic neuropathy, type 5 (HSAN5), and dysregulation of this gene's expression is associated with allergic rhinitis. [provided by RefSeq, Jul 2008]","start":115285918,"end":115338236,"strand":-1,"description":"nerve growth factor [Source:HGNC Symbol;Acc:HGNC:7808]"}, {"versioned_ensembl_gene_id":"ENSG00000242671.1","gene_symbol":"LINC02010","gene_name":"long intergenic non-protein coding RNA 2010 [Source:HGNC Symbol;Acc:HGNC:52846]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927866","summary":null,"start":146921923,"end":146925218,"strand":1,"description":"long intergenic non-protein coding RNA 2010 [Source:HGNC Symbol;Acc:HGNC:52846]"}, {"versioned_ensembl_gene_id":"ENSG00000259449.1","gene_symbol":"NIFKP8","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44956]","synonyms":"MKI67IPP8","biotype":"processed_pseudogene","ncbi_id":"642907","summary":null,"start":85181210,"end":85182083,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44956]"}, {"versioned_ensembl_gene_id":"ENSG00000107611.14","gene_symbol":"CUBN","gene_name":"cubilin [Source:HGNC Symbol;Acc:HGNC:2548]","synonyms":"MGA1,IFCR,gp280","biotype":"protein_coding","ncbi_id":"8029","summary":"Cubilin (CUBN) acts as a receptor for intrinsic factor-vitamin B12 complexes. The role of receptor is supported by the presence of 27 CUB domains. Cubulin is located within the epithelium of intestine and kidney. Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia. [provided by RefSeq, Jul 2008]","start":16823964,"end":17129831,"strand":-1,"description":"cubilin [Source:HGNC Symbol;Acc:HGNC:2548]"}, {"versioned_ensembl_gene_id":"ENSG00000281991.1","gene_symbol":"TMEM265","gene_name":"transmembrane protein 265 [Source:HGNC Symbol;Acc:HGNC:51241]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100862671","summary":null,"start":30740381,"end":30744281,"strand":1,"description":"transmembrane protein 265 [Source:HGNC Symbol;Acc:HGNC:51241]"}, {"versioned_ensembl_gene_id":"ENSG00000230733.2","gene_symbol":"AC092171.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5475804,"end":5479811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152443.12","gene_symbol":"ZNF776","gene_name":"zinc finger protein 776 [Source:HGNC Symbol;Acc:HGNC:26765]","synonyms":"FLJ38288","biotype":"protein_coding","ncbi_id":"284309","summary":null,"start":57746796,"end":57758159,"strand":1,"description":"zinc finger protein 776 [Source:HGNC Symbol;Acc:HGNC:26765]"}, {"versioned_ensembl_gene_id":"ENSG00000268392.1","gene_symbol":"AC003682.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57625032,"end":57626950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077549.17","gene_symbol":"CAPZB","gene_name":"capping actin protein of muscle Z-line beta subunit [Source:HGNC Symbol;Acc:HGNC:1491]","synonyms":null,"biotype":"protein_coding","ncbi_id":"832","summary":"This gene encodes the beta subunit of the barbed-end actin binding protein, which belongs to the F-actin capping protein family. The capping protein is a heterodimeric actin capping protein that blocks actin filament assembly and disassembly at the fast growing (barbed) filament ends and functions in regulating actin filament dynamics as well as in stabilizing actin filament lengths in muscle and nonmuscle cells. A pseudogene of this gene is located on the long arm of chromosome 2. Multiple alternatively spliced transcript variants encoding different isoforms have been found.[provided by RefSeq, Aug 2013]","start":19338776,"end":19485539,"strand":-1,"description":"capping actin protein of muscle Z-line beta subunit [Source:HGNC Symbol;Acc:HGNC:1491]"}, {"versioned_ensembl_gene_id":"ENSG00000219410.5","gene_symbol":"AC125494.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6663260,"end":6672069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185615.15","gene_symbol":"PDIA2","gene_name":"protein disulfide isomerase family A member 2 [Source:HGNC Symbol;Acc:HGNC:14180]","synonyms":"PDI,PDA2,PDIR,PDIP","biotype":"protein_coding","ncbi_id":"64714","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, two catalytically active thioredoxin (TRX) domains, two TRX-like domains and a C-terminal ER-retention sequence. The protein plays a role in the folding of nascent proteins in the endoplasmic reticulum by forming disulfide bonds through its thiol isomerase, oxidase, and reductase activity. The encoded protein also possesses estradiol-binding activity and can modulate intracellular estradiol levels. [provided by RefSeq, Sep 2017]","start":283152,"end":287215,"strand":1,"description":"protein disulfide isomerase family A member 2 [Source:HGNC Symbol;Acc:HGNC:14180]"}, {"versioned_ensembl_gene_id":"ENSG00000270850.1","gene_symbol":"AL356986.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32421979,"end":32422319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279124.1","gene_symbol":"AL356585.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18279320,"end":18309934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144847.12","gene_symbol":"IGSF11","gene_name":"immunoglobulin superfamily member 11 [Source:HGNC Symbol;Acc:HGNC:16669]","synonyms":"VSIG3,MGC35227,Igsf13,CT119,BT-IgSF","biotype":"protein_coding","ncbi_id":"152404","summary":"IGSF11 is an immunoglobulin (Ig) superfamily member that is preferentially expressed in brain and testis. It shares significant homology with coxsackievirus and adenovirus receptor (CXADR; MIM 602621) and endothelial cell-selective adhesion molecule (ESAM).[supplied by OMIM, Apr 2005]","start":118900557,"end":119146068,"strand":-1,"description":"immunoglobulin superfamily member 11 [Source:HGNC Symbol;Acc:HGNC:16669]"}, {"versioned_ensembl_gene_id":"ENSG00000142273.10","gene_symbol":"CBLC","gene_name":"Cbl proto-oncogene C [Source:HGNC Symbol;Acc:HGNC:15961]","synonyms":"RNF57,CBL-SL,CBL-3","biotype":"protein_coding","ncbi_id":"23624","summary":"This gene encodes a member of the Cbl family of E3 ubiquitin ligases. Cbl proteins play important roles in cell signaling through the ubiquitination and subsequent downregulation of tyrosine kinases. Expression of this gene may be restricted to epithelial cells, and alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":44777869,"end":44800634,"strand":1,"description":"Cbl proto-oncogene C [Source:HGNC Symbol;Acc:HGNC:15961]"}, {"versioned_ensembl_gene_id":"ENSG00000139679.15","gene_symbol":"LPAR6","gene_name":"lysophosphatidic acid receptor 6 [Source:HGNC Symbol;Acc:HGNC:15520]","synonyms":"P2RY5,P2Y5","biotype":"protein_coding","ncbi_id":"10161","summary":"The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene aligns with an internal intron of the retinoblastoma susceptibility gene in the reverse orientation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]","start":48389567,"end":48444704,"strand":-1,"description":"lysophosphatidic acid receptor 6 [Source:HGNC Symbol;Acc:HGNC:15520]"}, {"versioned_ensembl_gene_id":"ENSG00000280917.1","gene_symbol":"AC241851.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90359653,"end":90359876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258494.1","gene_symbol":"OR11J5P","gene_name":"olfactory receptor family 11 subfamily J member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31238]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403226","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20969282,"end":20970215,"strand":-1,"description":"olfactory receptor family 11 subfamily J member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31238]"}, {"versioned_ensembl_gene_id":"ENSG00000135477.11","gene_symbol":"KRT87P","gene_name":"keratin 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:30198]","synonyms":"KRTHBP4,KRT121P,HBD","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"85349","summary":null,"start":52250466,"end":52258867,"strand":-1,"description":"keratin 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:30198]"}, {"versioned_ensembl_gene_id":"ENSG00000204227.4","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33208495,"end":33212722,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000211701.2","gene_symbol":"TRGV1","gene_name":"T-cell receptor gamma variable 1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12284]","synonyms":"V1S1P,TCRGV1","biotype":"TR_V_gene","ncbi_id":"6973","summary":null,"start":38367586,"end":38368169,"strand":-1,"description":"T-cell receptor gamma variable 1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12284]"}, {"versioned_ensembl_gene_id":"ENSG00000227191.8","gene_symbol":"TRGC2","gene_name":"T-cell receptor gamma constant 2 [Source:HGNC Symbol;Acc:HGNC:12276]","synonyms":"TRGC2(3X),TRGC2(2X),TCRGC2","biotype":"TR_C_gene","ncbi_id":"6967","summary":null,"start":38239580,"end":38249572,"strand":-1,"description":"T-cell receptor gamma constant 2 [Source:HGNC Symbol;Acc:HGNC:12276]"}, {"versioned_ensembl_gene_id":"ENSG00000279516.1","gene_symbol":"FAM230C","gene_name":"family with sequence similarity 230 member C [Source:HGNC Symbol;Acc:HGNC:24482]","synonyms":"DKFZP434B061,NCRNA00281,LINC00281","biotype":"processed_transcript","ncbi_id":"26080","summary":null,"start":18195297,"end":18232024,"strand":1,"description":"family with sequence similarity 230 member C [Source:HGNC Symbol;Acc:HGNC:24482]"}, {"versioned_ensembl_gene_id":"ENSG00000261048.1","gene_symbol":"AC012414.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20890206,"end":20890606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234265.1","gene_symbol":"LINC01723","gene_name":"long intergenic non-protein coding RNA 1723 [Source:HGNC Symbol;Acc:HGNC:52511]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505515","summary":null,"start":12950338,"end":12951627,"strand":1,"description":"long intergenic non-protein coding RNA 1723 [Source:HGNC Symbol;Acc:HGNC:52511]"}, {"versioned_ensembl_gene_id":"ENSG00000183172.8","gene_symbol":"SMDT1","gene_name":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]","synonyms":"dJ186O1.1,DDDD,C22orf32,EMRE","biotype":"protein_coding","ncbi_id":"91689","summary":"This gene encodes a core regulatory component of a calcium channel in the mitochondrial inner membrane. [provided by RefSeq, Apr 2017]","start":42079691,"end":42084284,"strand":1,"description":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]"}, {"versioned_ensembl_gene_id":"ENSG00000121053.5","gene_symbol":"EPX","gene_name":"eosinophil peroxidase [Source:HGNC Symbol;Acc:HGNC:3423]","synonyms":"EPX-PEN,EPP,EPO","biotype":"protein_coding","ncbi_id":"8288","summary":"This gene is a member of the peroxidase gene family and is expressed in eosinophils. The encoded preproprotein is proteolytically processed into covalently attached heavy and light chains to form the mature enzyme, which functions as an oxidant. The enzyme is released at sites of parasitic infection or allergen stimulation to mediate lysis of protozoa or parasitic worms. The gene is found in a gene cluster with other peroxidase genes on chromosome 17. Mutations in this gene result in eosinophil peroxidase deficiency. [provided by RefSeq, Feb 2016]","start":58192737,"end":58205174,"strand":1,"description":"eosinophil peroxidase [Source:HGNC Symbol;Acc:HGNC:3423]"}, {"versioned_ensembl_gene_id":"ENSG00000137693.13","gene_symbol":"YAP1","gene_name":"Yes associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16262]","synonyms":"YAP65","biotype":"protein_coding","ncbi_id":"10413","summary":"This gene encodes a downstream nuclear effector of the Hippo signaling pathway which is involved in development, growth, repair, and homeostasis. This gene is known to play a role in the development and progression of multiple cancers as a transcriptional regulator of this signaling pathway and may function as a potential target for cancer treatment. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2013]","start":102110461,"end":102233423,"strand":1,"description":"Yes associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16262]"}, {"versioned_ensembl_gene_id":"ENSG00000227653.1","gene_symbol":"ISCA1P6","gene_name":"iron-sulfur cluster assembly 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38027]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130549","summary":null,"start":128518788,"end":128519177,"strand":-1,"description":"iron-sulfur cluster assembly 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38027]"}, {"versioned_ensembl_gene_id":"ENSG00000108846.15","gene_symbol":"ABCC3","gene_name":"ATP binding cassette subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:54]","synonyms":"MRP3,MOAT-D,MLP2,EST90757,cMOAT2","biotype":"protein_coding","ncbi_id":"8714","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. The specific function of this protein has not yet been determined; however, this protein may play a role in the transport of biliary and intestinal excretion of organic anions. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":50634777,"end":50692252,"strand":1,"description":"ATP binding cassette subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:54]"}, {"versioned_ensembl_gene_id":"ENSG00000276581.2","gene_symbol":"SPATA31A5","gene_name":"SPATA31 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:32005]","synonyms":"OTTHUMG00000013204,FAM75A5","biotype":"protein_coding","ncbi_id":"727905","summary":null,"start":60914374,"end":60920650,"strand":1,"description":"SPATA31 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:32005]"}, {"versioned_ensembl_gene_id":"ENSG00000170364.12","gene_symbol":"SETMAR","gene_name":"SET domain and mariner transposase fusion gene [Source:HGNC Symbol;Acc:HGNC:10762]","synonyms":"metnase","biotype":"protein_coding","ncbi_id":"6419","summary":"This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non-homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":4303304,"end":4317567,"strand":1,"description":"SET domain and mariner transposase fusion gene [Source:HGNC Symbol;Acc:HGNC:10762]"}, {"versioned_ensembl_gene_id":"ENSG00000105248.15","gene_symbol":"CCDC94","gene_name":"coiled-coil domain containing 94 [Source:HGNC Symbol;Acc:HGNC:25518]","synonyms":"FLJ10374","biotype":"protein_coding","ncbi_id":"55702","summary":null,"start":4247079,"end":4269090,"strand":1,"description":"coiled-coil domain containing 94 [Source:HGNC Symbol;Acc:HGNC:25518]"}, {"versioned_ensembl_gene_id":"ENSG00000213538.5","gene_symbol":"KRT8P41","gene_name":"keratin 8 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:39875]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283102","summary":null,"start":9094377,"end":9095890,"strand":1,"description":"keratin 8 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:39875]"}, {"versioned_ensembl_gene_id":"ENSG00000276876.4","gene_symbol":"MYT1","gene_name":"myelin transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7622]","synonyms":"ZC2H2C1,PLPB1,NZF2,MYTI,MTF1,ZC2HC4A","biotype":"protein_coding","ncbi_id":"4661","summary":"The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system. [provided by RefSeq, Jul 2008]","start":64155437,"end":64245898,"strand":1,"description":"myelin transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7622]"}, {"versioned_ensembl_gene_id":"ENSG00000236735.3","gene_symbol":"RPL31P63","gene_name":"ribosomal protein L31 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35666]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271392","summary":null,"start":68600099,"end":68600473,"strand":1,"description":"ribosomal protein L31 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35666]"}, {"versioned_ensembl_gene_id":"ENSG00000196092.12","gene_symbol":"PAX5","gene_name":"paired box 5 [Source:HGNC Symbol;Acc:HGNC:8619]","synonyms":"BSAP","biotype":"protein_coding","ncbi_id":"5079","summary":"This gene encodes a member of the paired box (PAX) family of transcription factors. The central feature of this gene family is a novel, highly conserved DNA-binding motif, known as the paired box. Paired box transcription factors are important regulators in early development, and alterations in the expression of their genes are thought to contribute to neoplastic transformation. This gene encodes the B-cell lineage specific activator protein that is expressed at early, but not late stages of B-cell differentiation. Its expression has also been detected in developing CNS and testis and so the encoded protein may also play a role in neural development and spermatogenesis. This gene is located at 9p13, which is involved in t(9;14)(p13;q32) translocations recurring in small lymphocytic lymphomas of the plasmacytoid subtype, and in derived large-cell lymphomas. This translocation brings the potent E-mu enhancer of the IgH gene into close proximity of the PAX5 promoter, suggesting that the deregulation of transcription of this gene contributes to the pathogenesis of these lymphomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":36833275,"end":37034185,"strand":-1,"description":"paired box 5 [Source:HGNC Symbol;Acc:HGNC:8619]"}, {"versioned_ensembl_gene_id":"ENSG00000225718.1","gene_symbol":"AC092100.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69224696,"end":69430923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267273.1","gene_symbol":"AC008567.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9498678,"end":9510079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248209.1","gene_symbol":"AC097462.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127493505,"end":127493828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226374.2","gene_symbol":"LINC01345","gene_name":"long intergenic non-protein coding RNA 1345 [Source:HGNC Symbol;Acc:HGNC:50564]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376672","summary":null,"start":3944547,"end":3948980,"strand":-1,"description":"long intergenic non-protein coding RNA 1345 [Source:HGNC Symbol;Acc:HGNC:50564]"}, {"versioned_ensembl_gene_id":"ENSG00000225610.1","gene_symbol":"AC007679.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":205989585,"end":206000858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225664.3","gene_symbol":"YWHAZP8","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39029]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646016","summary":null,"start":73274785,"end":73275515,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39029]"}, {"versioned_ensembl_gene_id":"ENSG00000164512.17","gene_symbol":"ANKRD55","gene_name":"ankyrin repeat domain 55 [Source:HGNC Symbol;Acc:HGNC:25681]","synonyms":"FLJ11795","biotype":"protein_coding","ncbi_id":"79722","summary":null,"start":56099678,"end":56233359,"strand":-1,"description":"ankyrin repeat domain 55 [Source:HGNC Symbol;Acc:HGNC:25681]"}, {"versioned_ensembl_gene_id":"ENSG00000162433.14","gene_symbol":"AK4","gene_name":"adenylate kinase 4 [Source:HGNC Symbol;Acc:HGNC:363]","synonyms":"AK3,AK3L1","biotype":"protein_coding","ncbi_id":"205","summary":"This gene encodes a member of the adenylate kinase family of enzymes. The encoded protein is localized to the mitochondrial matrix. Adenylate kinases regulate the adenine and guanine nucleotide compositions within a cell by catalyzing the reversible transfer of phosphate group among these nucleotides. Five isozymes of adenylate kinase have been identified in vertebrates. Expression of these isozymes is tissue-specific and developmentally regulated. A pseudogene for this gene has been located on chromosome 17. Three transcript variants encoding the same protein have been identified for this gene. Sequence alignment suggests that the gene defined by NM_013410, NM_203464, and NM_001005353 is located on chromosome 1. [provided by RefSeq, Jul 2008]","start":65147549,"end":65232145,"strand":1,"description":"adenylate kinase 4 [Source:HGNC Symbol;Acc:HGNC:363]"}, {"versioned_ensembl_gene_id":"ENSG00000254957.1","gene_symbol":"AC111188.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11135482,"end":11137658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196914.8","gene_symbol":"ARHGEF12","gene_name":"Rho guanine nucleotide exchange factor 12 [Source:HGNC Symbol;Acc:HGNC:14193]","synonyms":"LARG,KIAA0382","biotype":"protein_coding","ncbi_id":"23365","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli working through G protein-coupled receptors. The encoded protein may form a complex with G proteins and stimulate Rho-dependent signals. This protein has been observed to form a myeloid/lymphoid fusion partner in acute myeloid leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":120336914,"end":120489936,"strand":1,"description":"Rho guanine nucleotide exchange factor 12 [Source:HGNC Symbol;Acc:HGNC:14193]"}, {"versioned_ensembl_gene_id":"ENSG00000238213.1","gene_symbol":"TARDBPP2","gene_name":"TAR DNA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39848]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440142","summary":null,"start":60274776,"end":60276006,"strand":1,"description":"TAR DNA binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39848]"}, {"versioned_ensembl_gene_id":"ENSG00000111981.4","gene_symbol":"ULBP1","gene_name":"UL16 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:14893]","synonyms":"RAET1I","biotype":"protein_coding","ncbi_id":"80329","summary":"The protein encoded by this gene is a ligand of natural killer group 2, member D (NKG2D), an immune system-activating receptor on NK cells and T-cells. Binding of the encoded ligand to NKG2D leads to activation of several signal transduction pathways, including those of JAK2, STAT5, ERK and PI3K kinase/Akt. Also, in cytomegalovirus-infected cells, this ligand binds the UL16 glycoprotein and is prevented from activating the immune system. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":149964007,"end":149973710,"strand":1,"description":"UL16 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:14893]"}, {"versioned_ensembl_gene_id":"ENSG00000259087.5","gene_symbol":"AL121790.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37556158,"end":37567095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169744.12","gene_symbol":"LDB2","gene_name":"LIM domain binding 2 [Source:HGNC Symbol;Acc:HGNC:6533]","synonyms":"LDB1,CLIM1","biotype":"protein_coding","ncbi_id":"9079","summary":"The protein encoded by this gene belongs to the LIM-domain binding family. Members of this family are characterized by a conserved nuclear localization sequence, an amino-terminal homodimerization domain and a carboxy-terminal LIM interaction domain. These proteins function as adapter molecules to allow assembly of transcriptional regulatory complexes. Genetic association studies suggest functions for this gene in rhegmatogenous retinal detachment and coronary artery disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":16501541,"end":16898809,"strand":-1,"description":"LIM domain binding 2 [Source:HGNC Symbol;Acc:HGNC:6533]"}, {"versioned_ensembl_gene_id":"ENSG00000275965.1","gene_symbol":"AC091544.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92634305,"end":92634665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256034.1","gene_symbol":"AP002770.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73760563,"end":73761070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273773.1","gene_symbol":"AC244107.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154620096,"end":154620171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186230.6","gene_symbol":"ZNF749","gene_name":"zinc finger protein 749 [Source:HGNC Symbol;Acc:HGNC:32783]","synonyms":"FLJ16360","biotype":"protein_coding","ncbi_id":"388567","summary":null,"start":57435329,"end":57445485,"strand":1,"description":"zinc finger protein 749 [Source:HGNC Symbol;Acc:HGNC:32783]"}, {"versioned_ensembl_gene_id":"ENSG00000226379.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29788736,"end":29789733,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000254534.1","gene_symbol":"AP000776.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101765935,"end":101769961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254648.1","gene_symbol":"AP000911.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134035832,"end":134037107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112486.15","gene_symbol":"CCR6","gene_name":"C-C motif chemokine receptor 6 [Source:HGNC Symbol;Acc:HGNC:1607]","synonyms":"BN-1,STRL22,GPR29,GPR-CY4,DRY-6,DCR2,CMKBR6,CKR-L3,CD196","biotype":"protein_coding","ncbi_id":"1235","summary":"This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. The gene is preferentially expressed by immature dendritic cells and memory T cells. The ligand of this receptor is macrophage inflammatory protein 3 alpha (MIP-3 alpha). This receptor has been shown to be important for B-lineage maturation and antigen-driven B-cell differentiation, and it may regulate the migration and recruitment of dentritic and T cells during inflammatory and immunological responses. Alternatively spliced transcript variants that encode the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":167111807,"end":167139696,"strand":1,"description":"C-C motif chemokine receptor 6 [Source:HGNC Symbol;Acc:HGNC:1607]"}, {"versioned_ensembl_gene_id":"ENSG00000196378.11","gene_symbol":"ZNF34","gene_name":"zinc finger protein 34 [Source:HGNC Symbol;Acc:HGNC:13098]","synonyms":"KOX32","biotype":"protein_coding","ncbi_id":"80778","summary":null,"start":144773114,"end":144787345,"strand":-1,"description":"zinc finger protein 34 [Source:HGNC Symbol;Acc:HGNC:13098]"}, {"versioned_ensembl_gene_id":"ENSG00000167100.14","gene_symbol":"SAMD14","gene_name":"sterile alpha motif domain containing 14 [Source:HGNC Symbol;Acc:HGNC:27312]","synonyms":"FLJ36890","biotype":"protein_coding","ncbi_id":"201191","summary":null,"start":50110040,"end":50129882,"strand":-1,"description":"sterile alpha motif domain containing 14 [Source:HGNC Symbol;Acc:HGNC:27312]"}, {"versioned_ensembl_gene_id":"ENSG00000250149.1","gene_symbol":"AC105919.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125676718,"end":125752793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110318.13","gene_symbol":"CEP126","gene_name":"centrosomal protein 126 [Source:HGNC Symbol;Acc:HGNC:29264]","synonyms":"KIAA1377","biotype":"protein_coding","ncbi_id":"57562","summary":null,"start":101915015,"end":102001058,"strand":1,"description":"centrosomal protein 126 [Source:HGNC Symbol;Acc:HGNC:29264]"}, {"versioned_ensembl_gene_id":"ENSG00000282028.1","gene_symbol":"AC015938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36685736,"end":36686111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237312.1","gene_symbol":"AL590867.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153304595,"end":153308982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185565.11","gene_symbol":"LSAMP","gene_name":"limbic system-associated membrane protein [Source:HGNC Symbol;Acc:HGNC:6705]","synonyms":"LAMP,IGLON3","biotype":"protein_coding","ncbi_id":"4045","summary":"This gene encodes a member of the immunoglobulin LAMP, OBCAM and neurotrimin (IgLON) family of proteins. The encoded preproprotein is proteolytically processed to generate a neuronal surface glycoprotein. This protein may act as a selective homophilic adhesion molecule during axon guidance and neuronal growth in the developing limbic system. The encoded protein may also function as a tumor suppressor and may play a role in neuropsychiatric disorders. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":115802363,"end":117139389,"strand":-1,"description":"limbic system-associated membrane protein [Source:HGNC Symbol;Acc:HGNC:6705]"}, {"versioned_ensembl_gene_id":"ENSG00000086666.18","gene_symbol":"ZFAND6","gene_name":"zinc finger AN1-type containing 6 [Source:HGNC Symbol;Acc:HGNC:30164]","synonyms":"ZFAND5B,ZA20D3,AWP1","biotype":"protein_coding","ncbi_id":"54469","summary":null,"start":80059568,"end":80138393,"strand":1,"description":"zinc finger AN1-type containing 6 [Source:HGNC Symbol;Acc:HGNC:30164]"}, {"versioned_ensembl_gene_id":"ENSG00000236039.2","gene_symbol":"AC019117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17405479,"end":17558909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278254.4","gene_symbol":"AC004852.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9082557,"end":9189857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267272.5","gene_symbol":"LINC01140","gene_name":"long intergenic non-protein coding RNA 1140 [Source:HGNC Symbol;Acc:HGNC:27922]","synonyms":"FLJ41676","biotype":"lincRNA","ncbi_id":"339524","summary":null,"start":87129765,"end":87169198,"strand":1,"description":"long intergenic non-protein coding RNA 1140 [Source:HGNC Symbol;Acc:HGNC:27922]"}, {"versioned_ensembl_gene_id":"ENSG00000258590.5","gene_symbol":"NBEAP1","gene_name":"neurobeachin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1007]","synonyms":"BCL8A,BCL8","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"606","summary":null,"start":20657638,"end":20688408,"strand":-1,"description":"neurobeachin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1007]"}, {"versioned_ensembl_gene_id":"ENSG00000129465.15","gene_symbol":"RIPK3","gene_name":"receptor interacting serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:10021]","synonyms":"RIP3","biotype":"protein_coding","ncbi_id":"11035","summary":"The product of this gene is a member of the receptor-interacting protein (RIP) family of serine/threonine protein kinases, and contains a C-terminal domain unique from other RIP family members. The encoded protein is predominantly localized to the cytoplasm, and can undergo nucleocytoplasmic shuttling dependent on novel nuclear localization and export signals. It is a component of the tumor necrosis factor (TNF) receptor-I signaling complex, and can induce apoptosis and weakly activate the NF-kappaB transcription factor. [provided by RefSeq, Jul 2008]","start":24336021,"end":24340045,"strand":-1,"description":"receptor interacting serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:10021]"}, {"versioned_ensembl_gene_id":"ENSG00000236318.2","gene_symbol":"AC019117.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17374867,"end":17467256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153936.16","gene_symbol":"HS2ST1","gene_name":"heparan sulfate 2-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5193]","synonyms":"KIAA0448","biotype":"protein_coding","ncbi_id":"9653","summary":"Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. This gene encodes a member of the heparan sulfate biosynthetic enzyme family that transfers sulfate to the 2 position of the iduronic acid residue of heparan sulfate. The disruption of this gene resulted in no kidney formation in knockout embryonic mice, indicating that the absence of this enzyme may interfere with the signaling required for kidney formation. Two alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Aug 2008]","start":86914648,"end":87109998,"strand":1,"description":"heparan sulfate 2-O-sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:5193]"}, {"versioned_ensembl_gene_id":"ENSG00000255951.1","gene_symbol":"AC022364.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28164958,"end":28165662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272008.1","gene_symbol":"AL139274.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87151159,"end":87155285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236415.4","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31506943,"end":31507754,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000258916.2","gene_symbol":"SPATA31E2P","gene_name":"SPATA31 subfamily E member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:43827]","synonyms":"FAM75E2P","biotype":"unprocessed_pseudogene","ncbi_id":"646177","summary":null,"start":20593494,"end":20599195,"strand":-1,"description":"SPATA31 subfamily E member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:43827]"}, {"versioned_ensembl_gene_id":"ENSG00000048140.17","gene_symbol":"TSPAN17","gene_name":"tetraspanin 17 [Source:HGNC Symbol;Acc:HGNC:13594]","synonyms":"TM4SF17,FBXO23,FBX23","biotype":"protein_coding","ncbi_id":"26262","summary":"This gene encodes a member of the transmembrane 4 superfamily. It is characterized by four tetraspanin transmembrane segments. The function of this gene has not yet been determined. [provided by RefSeq, Mar 2014]","start":176647387,"end":176659054,"strand":1,"description":"tetraspanin 17 [Source:HGNC Symbol;Acc:HGNC:13594]"}, {"versioned_ensembl_gene_id":"ENSG00000164638.10","gene_symbol":"SLC29A4","gene_name":"solute carrier family 29 member 4 [Source:HGNC Symbol;Acc:HGNC:23097]","synonyms":"FLJ34923,ENT4","biotype":"protein_coding","ncbi_id":"222962","summary":"This gene encodes a member of the SLC29A/ENT transporter protein family. The encoded membrane protein catalyzes the reuptake of monoamines into presynaptic neurons, thus determining the intensity and duration of monoamine neural signaling. It has been shown to transport several compounds, including serotonin, dopamine, and the neurotoxin 1-methyl-4-phenylpyridinium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":5274369,"end":5306870,"strand":1,"description":"solute carrier family 29 member 4 [Source:HGNC Symbol;Acc:HGNC:23097]"}, {"versioned_ensembl_gene_id":"ENSG00000283709.1","gene_symbol":"FAM238C","gene_name":"family with sequence similarity 238 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:24672]","synonyms":"NCRNA00202,LINC00202-1,LINC00202,C10orf51,bB27G4.1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387644","summary":null,"start":26931206,"end":26944418,"strand":-1,"description":"family with sequence similarity 238 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:24672]"}, {"versioned_ensembl_gene_id":"ENSG00000253973.2","gene_symbol":"AC079296.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9004162,"end":9065154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117054.13","gene_symbol":"ACADM","gene_name":"acyl-CoA dehydrogenase, C-4 to C-12 straight chain [Source:HGNC Symbol;Acc:HGNC:89]","synonyms":"MCADH,MCAD,ACAD1","biotype":"protein_coding","ncbi_id":"34","summary":"This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75724347,"end":75787575,"strand":1,"description":"acyl-CoA dehydrogenase, C-4 to C-12 straight chain [Source:HGNC Symbol;Acc:HGNC:89]"}, {"versioned_ensembl_gene_id":"ENSG00000227389.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BPG309N1.15,BAT1P2","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":30071672,"end":30072068,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000270585.1","gene_symbol":"AL445435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220207618,"end":220208282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276400.1","gene_symbol":"VN1R9P","gene_name":"vomeronasal 1 receptor 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:20257]","synonyms":"VN1R22-1P","biotype":"processed_pseudogene","ncbi_id":"317691","summary":null,"start":17021398,"end":17022570,"strand":-1,"description":"vomeronasal 1 receptor 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:20257]"}, {"versioned_ensembl_gene_id":"ENSG00000233151.6","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"CA21H,P450c21B,CPS1,CYP21B,CAH1,CYP21","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31986739,"end":31990111,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000136573.12","gene_symbol":"BLK","gene_name":"BLK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1057]","synonyms":"MGC10442","biotype":"protein_coding","ncbi_id":"640","summary":"This gene encodes a nonreceptor tyrosine-kinase of the src family of proto-oncogenes that are typically involved in cell proliferation and differentiation. The protein has a role in B-cell receptor signaling and B-cell development. The protein also stimulates insulin synthesis and secretion in response to glucose and enhances the expression of several pancreatic beta-cell transcription factors. [provided by RefSeq, Aug 2010]","start":11494001,"end":11564604,"strand":1,"description":"BLK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1057]"}, {"versioned_ensembl_gene_id":"ENSG00000255518.1","gene_symbol":"AC022239.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11556251,"end":11558022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127948.15","gene_symbol":"POR","gene_name":"cytochrome p450 oxidoreductase [Source:HGNC Symbol;Acc:HGNC:9208]","synonyms":"FLJ26468,CYPOR","biotype":"protein_coding","ncbi_id":"5447","summary":"This gene encodes an endoplasmic reticulum membrane oxidoreductase that is essential for multiple metabolic processes, including reactions catalyzed by cytochrome P450 proteins for metabolism of steroid hormones, drugs and xenobiotics. The encoded protein has a flavin adenine dinucleotide (FAD)-binding domain and a flavodoxin-like domain which bind two cofactors, FAD and FMN, that allow it to donate electrons directly from NADPH to all microsomal P450 enzymes. Mutations in this gene cause a complex set of disorders, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal hyperplasia and Antley-Bixler syndrome, that resemble those caused by defects in steroid metabolizing enzymes such as aromatase, 21-hydroxylase, and 17 alpha-hydroxylase. [provided by RefSeq, Aug 2020]","start":75899200,"end":75986855,"strand":1,"description":"cytochrome p450 oxidoreductase [Source:HGNC Symbol;Acc:HGNC:9208]"}, {"versioned_ensembl_gene_id":"ENSG00000214525.4","gene_symbol":"AC130709.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68528241,"end":68529452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151532.13","gene_symbol":"VTI1A","gene_name":"vesicle transport through interaction with t-SNAREs 1A [Source:HGNC Symbol;Acc:HGNC:17792]","synonyms":"Vti1a,Vti1-rp2,MVti1","biotype":"protein_coding","ncbi_id":"143187","summary":"The protein encoded by this gene is a member of the family of soluble N-ethylmaleimide-sensitive fusion protein-attachment protein receptors (SNAREs) that function in intracellular trafficking. This family member is involved in vesicular transport between endosomes and the trans-Golgi network. It is a vesicle-associated SNARE (v-SNARE) that interacts with target membrane SNAREs (t-SNAREs). Polymorphisms in this gene have been associated with binocular function, and also with susceptibility to colorectal and lung cancers. A recurrent rearrangement has been found between this gene and the transcription factor 7-like 2 (TCF7L2) gene in colorectal cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":112446998,"end":112818744,"strand":1,"description":"vesicle transport through interaction with t-SNAREs 1A [Source:HGNC Symbol;Acc:HGNC:17792]"}, {"versioned_ensembl_gene_id":"ENSG00000229769.2","gene_symbol":"TRBV10-2","gene_name":"T-cell receptor beta variable 10-2 [Source:HGNC Symbol;Acc:HGNC:12178]","synonyms":"TRBV102,TCRBV12S3,TCRBV10S2","biotype":"TR_V_gene","ncbi_id":"28584","summary":null,"start":142424965,"end":142425465,"strand":1,"description":"T-cell receptor beta variable 10-2 [Source:HGNC Symbol;Acc:HGNC:12178]"}, {"versioned_ensembl_gene_id":"ENSG00000236531.2","gene_symbol":"AC006013.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68091223,"end":68119209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107949.16","gene_symbol":"BCCIP","gene_name":"BRCA2 and CDKN1A interacting protein [Source:HGNC Symbol;Acc:HGNC:978]","synonyms":"TOK-1,BCCIPalpha","biotype":"protein_coding","ncbi_id":"56647","summary":"This gene product was isolated on the basis of its interaction with BRCA2 and p21 proteins. It is an evolutionarily conserved nuclear protein with multiple interacting domains. The N-terminal half shares moderate homology with regions of calmodulin and M-calpain, suggesting that it may also bind calcium. Functional studies indicate that this protein may be an important cofactor for BRCA2 in tumor suppression, and a modulator of CDK2 kinase activity via p21. This protein has also been implicated in the regulation of BRCA2 and RAD51 nuclear focus formation, double-strand break-induced homologous recombination, and cell cycle progression. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":125823546,"end":125853695,"strand":1,"description":"BRCA2 and CDKN1A interacting protein [Source:HGNC Symbol;Acc:HGNC:978]"}, {"versioned_ensembl_gene_id":"ENSG00000116574.5","gene_symbol":"RHOU","gene_name":"ras homolog family member U [Source:HGNC Symbol;Acc:HGNC:17794]","synonyms":"WRCH1,WRCH-1,hG28K,FLJ10616,fJ646B12.2,DJ646B12.2,CDC42L1,ARHU","biotype":"protein_coding","ncbi_id":"58480","summary":"This gene encodes a member of the Rho family of GTPases. This protein can activate PAK1 and JNK1, and can induce filopodium formation and stress fiber dissolution. It may also mediate the effects of WNT1 signaling in the regulation of cell morphology, cytoskeletal organization, and cell proliferation. A non-coding transcript variant of this gene results from naturally occurring read-through transcription between this locus and the neighboring DUSP5P (dual specificity phosphatase 5 pseudogene) locus.[provided by RefSeq, Mar 2011]","start":228735077,"end":228746669,"strand":1,"description":"ras homolog family member U [Source:HGNC Symbol;Acc:HGNC:17794]"}, {"versioned_ensembl_gene_id":"ENSG00000270339.3","gene_symbol":"AC243756.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":146344131,"end":146344790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249737.1","gene_symbol":"AC020980.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16428536,"end":16432436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276509.1","gene_symbol":"AC239799.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146235806,"end":146237807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249828.2","gene_symbol":"AC118282.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49203171,"end":49203726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106541.11","gene_symbol":"AGR2","gene_name":"anterior gradient 2, protein disulphide isomerase family member [Source:HGNC Symbol;Acc:HGNC:328]","synonyms":"XAG-2,PDIA17,HAG-2,AG2","biotype":"protein_coding","ncbi_id":"10551","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, and a C-terminal ER-retention sequence. This protein plays a role in cell migration, cellular transformation and metastasis and is as a p53 inhibitor. As an ER-localized molecular chaperone, it plays a role in the folding, trafficking, and assembly of cysteine-rich transmembrane receptors and the cysteine-rich intestinal gylcoprotein mucin. This gene has been implicated in inflammatory bowel disease and cancer progression. [provided by RefSeq, Mar 2017]","start":16791811,"end":16833433,"strand":-1,"description":"anterior gradient 2, protein disulphide isomerase family member [Source:HGNC Symbol;Acc:HGNC:328]"}, {"versioned_ensembl_gene_id":"ENSG00000258925.2","gene_symbol":"NPM1P5","gene_name":"nucleophosmin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:7925]","synonyms":"NPMP5,NG5-4","biotype":"processed_pseudogene","ncbi_id":"4874","summary":null,"start":92285841,"end":92286678,"strand":1,"description":"nucleophosmin 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:7925]"}, {"versioned_ensembl_gene_id":"ENSG00000227719.1","gene_symbol":"AC006042.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8114025,"end":8116561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279497.1","gene_symbol":"AP003784.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132771623,"end":132773371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283209.1","gene_symbol":"AC106858.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56803841,"end":56804269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152700.13","gene_symbol":"SAR1B","gene_name":"secretion associated Ras related GTPase 1B [Source:HGNC Symbol;Acc:HGNC:10535]","synonyms":"SARA2","biotype":"protein_coding","ncbi_id":"51128","summary":"The protein encoded by this gene is a small GTPase that acts as a homodimer. The encoded protein is activated by the guanine nucleotide exchange factor PREB and is involved in protein transport from the endoplasmic reticulum to the Golgi. This protein is part of the COPII coat complex. Defects in this gene are a cause of chylomicron retention disease (CMRD), also known as Anderson disease (ANDD). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Mar 2010]","start":134601144,"end":134649271,"strand":-1,"description":"secretion associated Ras related GTPase 1B [Source:HGNC Symbol;Acc:HGNC:10535]"}, {"versioned_ensembl_gene_id":"ENSG00000244083.1","gene_symbol":"AC021205.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122815771,"end":122816117,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153933.9","gene_symbol":"DGKE","gene_name":"diacylglycerol kinase epsilon [Source:HGNC Symbol;Acc:HGNC:2852]","synonyms":"DGK,DAGK6","biotype":"protein_coding","ncbi_id":"8526","summary":"Diacylglycerol kinases are thought to be involved mainly in the regeneration of phosphatidylinositol (PI) from diacylglycerol in the PI-cycle during cell signal transduction. When expressed in mammalian cells, DGK-epsilon shows specificity for arachidonyl-containing diacylglycerol. DGK-epsilon is expressed predominantly in testis. [provided by RefSeq, Jul 2008]","start":56834099,"end":56869567,"strand":1,"description":"diacylglycerol kinase epsilon [Source:HGNC Symbol;Acc:HGNC:2852]"}, {"versioned_ensembl_gene_id":"ENSG00000270421.1","gene_symbol":"AC022022.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63358745,"end":63359104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279405.1","gene_symbol":"AC004696.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56480397,"end":56483977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161267.11","gene_symbol":"BDH1","gene_name":"3-hydroxybutyrate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:1027]","synonyms":"SDR9C1,BDH","biotype":"protein_coding","ncbi_id":"622","summary":"This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":197509783,"end":197573323,"strand":-1,"description":"3-hydroxybutyrate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:1027]"}, {"versioned_ensembl_gene_id":"ENSG00000134830.5","gene_symbol":"C5AR2","gene_name":"complement component 5a receptor 2 [Source:HGNC Symbol;Acc:HGNC:4527]","synonyms":"GPR77,C5L2","biotype":"protein_coding","ncbi_id":"27202","summary":"This gene encodes a G-protein coupled receptor 1 family member involved in the complement system of the innate immune response. Unlike classical G-protein coupled receptors, the encoded protein does not associate with intracellular G-proteins. It may instead modulate signal transduction through the beta-arrestin pathway, and may alternatively act as a decoy receptor. This gene may be involved in coronary artery disease and in the pathogenesis of sepsis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":47332147,"end":47347327,"strand":1,"description":"complement component 5a receptor 2 [Source:HGNC Symbol;Acc:HGNC:4527]"}, {"versioned_ensembl_gene_id":"ENSG00000267628.1","gene_symbol":"AC104423.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79253577,"end":79254856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267015.1","gene_symbol":"AC023090.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79340258,"end":79343972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167984.17","gene_symbol":"NLRC3","gene_name":"NLR family CARD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29889]","synonyms":"NOD3,FLJ00348,CLR16.2","biotype":"protein_coding","ncbi_id":"197358","summary":"This gene encodes a NOD-like receptor family member. The encoded protein is a cytosolic regulator of innate immunity. This protein directly interacts with stimulator of interferon genes (STING), to prevent its proper trafficking, resulting in disruption of STING-dependent activation of the innate immune response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":3539033,"end":3577400,"strand":-1,"description":"NLR family CARD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29889]"}, {"versioned_ensembl_gene_id":"ENSG00000234278.3","gene_symbol":"PRR20E","gene_name":"proline rich 20E [Source:HGNC Symbol;Acc:HGNC:37223]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729250","summary":"This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008]","start":57167197,"end":57170218,"strand":1,"description":"proline rich 20E [Source:HGNC Symbol;Acc:HGNC:37223]"}, {"versioned_ensembl_gene_id":"ENSG00000274642.1","gene_symbol":"AC244669.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":120197085,"end":120319680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081059.19","gene_symbol":"TCF7","gene_name":"transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:11639]","synonyms":"TCF-1","biotype":"protein_coding","ncbi_id":"6932","summary":"This gene encodes a member of the T-cell factor/lymphoid enhancer-binding factor family of high mobility group (HMG) box transcriptional activators. This gene is expressed predominantly in T-cells and plays a critical role in natural killer cell and innate lymphoid cell development. The encoded protein forms a complex with beta-catenin and activates transcription through a Wnt/beta-catenin signaling pathway. Mice with a knockout of this gene are viable and fertile, but display a block in T-lymphocyte differentiation. Alternative splicing results in multiple transcript variants. Naturally-occurring isoforms lacking the N-terminal beta-catenin interaction domain may act as dominant negative regulators of Wnt signaling. [provided by RefSeq, Oct 2016]","start":134114711,"end":134151865,"strand":1,"description":"transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:11639]"}, {"versioned_ensembl_gene_id":"ENSG00000250625.1","gene_symbol":"AL031073.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":142194352,"end":142195490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258609.2","gene_symbol":"LINC-ROR","gene_name":"long intergenic non-protein coding RNA, regulator of reprogramming [Source:HGNC Symbol;Acc:HGNC:43773]","synonyms":"ROR,lincRNA-ST8SIA3,lincRNA-RoR","biotype":"lincRNA","ncbi_id":"100885779","summary":"This gene produces a long non-coding RNA that regulates the reprogramming of pluripotent stem cells. This RNA suppresses induction of tumor protein p53 after DNA damage. It is thought to act as a sponge for microRNAs that regulate stem cell factors POU class 5 homeobox 1, Nanog, and SRY-box 2. This RNA may also have a extracellular role in modulating response to hypoxia in hepatocellular cancer cells. Expression of this transcript is associated with tumor progression and epithelial to mesenchymal transition and metastasis. [provided by RefSeq, Dec 2017]","start":57054559,"end":57072119,"strand":-1,"description":"long intergenic non-protein coding RNA, regulator of reprogramming [Source:HGNC Symbol;Acc:HGNC:43773]"}, {"versioned_ensembl_gene_id":"ENSG00000150540.13","gene_symbol":"HNMT","gene_name":"histamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:5028]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3176","summary":"In mammals, histamine is metabolized by two major pathways: N(tau)-methylation via histamine N-methyltransferase and oxidative deamination via diamine oxidase. This gene encodes the first enzyme which is found in the cytosol and uses S-adenosyl-L-methionine as the methyl donor. In the mammalian brain, the neurotransmitter activity of histamine is controlled by N(tau)-methylation as diamine oxidase is not found in the central nervous system. A common genetic polymorphism affects the activity levels of this gene product in red blood cells. Multiple alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Jul 2008]","start":137964020,"end":138016364,"strand":1,"description":"histamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:5028]"}, {"versioned_ensembl_gene_id":"ENSG00000220924.4","gene_symbol":"OSTCP4","gene_name":"oligosaccharyltransferase complex subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645264","summary":null,"start":112685055,"end":112685503,"strand":1,"description":"oligosaccharyltransferase complex subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42866]"}, {"versioned_ensembl_gene_id":"ENSG00000271538.5","gene_symbol":"LINC02427","gene_name":"long intergenic non-protein coding RNA 2427 [Source:HGNC Symbol;Acc:HGNC:53358]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377585","summary":null,"start":184506460,"end":184537554,"strand":-1,"description":"long intergenic non-protein coding RNA 2427 [Source:HGNC Symbol;Acc:HGNC:53358]"}, {"versioned_ensembl_gene_id":"ENSG00000223844.1","gene_symbol":"CR933540.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32682668,"end":32683798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273406.1","gene_symbol":"AC245008.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120076616,"end":120077091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224825.2","gene_symbol":"RORB-AS1","gene_name":"RORB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49803]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103752585","summary":null,"start":74485551,"end":74499127,"strand":-1,"description":"RORB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49803]"}, {"versioned_ensembl_gene_id":"ENSG00000074935.13","gene_symbol":"TUBE1","gene_name":"tubulin epsilon 1 [Source:HGNC Symbol;Acc:HGNC:20775]","synonyms":"TUBE,FLJ22589,dJ142L7.2","biotype":"protein_coding","ncbi_id":"51175","summary":"This gene encodes a member of the tubulin superfamily. This protein localizes to the centriolar sub-distal appendages that are associated with the older of the two centrioles after centrosome duplication. This protein plays a central role in organization of the microtubules during centriole duplication. A pseudogene of this gene is found on chromosome 5.[provided by RefSeq, Jan 2009]","start":112070777,"end":112087529,"strand":-1,"description":"tubulin epsilon 1 [Source:HGNC Symbol;Acc:HGNC:20775]"}, {"versioned_ensembl_gene_id":"ENSG00000183020.13","gene_symbol":"AP2A2","gene_name":"adaptor related protein complex 2 alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:562]","synonyms":"HIP9,DKFZP564D1864,CLAPA2,ADTAB,KIAA0899,HYPJ","biotype":"protein_coding","ncbi_id":"161","summary":"The protein encoded by this gene is a subunit of the AP-2 adaptor protein complex, which is involved in linking lipid and protein membrane components with the clathrin lattice. This interaction supports the formation of clathrin-coated vesicles, and the encoded subunit aids in the process by binding polyphosphoinositide-containing lipids in the cell membrane. [provided by RefSeq, Nov 2016]","start":924894,"end":1012245,"strand":1,"description":"adaptor related protein complex 2 alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:562]"}, {"versioned_ensembl_gene_id":"ENSG00000273978.1","gene_symbol":"AC005066.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87867601,"end":87868607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004975.11","gene_symbol":"DVL2","gene_name":"dishevelled segment polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:3086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1856","summary":"This gene encodes a member of the dishevelled (dsh) protein family. The vertebrate dsh proteins have approximately 40% amino acid sequence similarity with Drosophila dsh. This gene encodes a 90-kD protein that undergoes posttranslational phosphorylation to form a 95-kD cytoplasmic protein, which may play a role in the signal transduction pathway mediated by multiple Wnt proteins. The mechanisms of dishevelled function in Wnt signaling are likely to be conserved among metazoans. [provided by RefSeq, Jul 2008]","start":7225341,"end":7234545,"strand":-1,"description":"dishevelled segment polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:3086]"}, {"versioned_ensembl_gene_id":"ENSG00000259855.1","gene_symbol":"AC007749.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216995906,"end":216996490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248498.4","gene_symbol":"ASNSP1","gene_name":"asparagine synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:754]","synonyms":"ASNSL1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"389652","summary":null,"start":46579213,"end":46638886,"strand":-1,"description":"asparagine synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:754]"}, {"versioned_ensembl_gene_id":"ENSG00000243830.2","gene_symbol":"AC092865.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8460618,"end":8461232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177586.6","gene_symbol":"AC092865.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8437403,"end":8438425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238152.2","gene_symbol":"AC092865.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8414780,"end":8415805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256136.1","gene_symbol":"AC092865.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8406833,"end":8407195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258083.2","gene_symbol":"OR9A4","gene_name":"olfactory receptor family 9 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:15095]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130075","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":141916399,"end":141920625,"strand":1,"description":"olfactory receptor family 9 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:15095]"}, {"versioned_ensembl_gene_id":"ENSG00000257138.1","gene_symbol":"TAS2R38","gene_name":"taste 2 receptor member 38 [Source:HGNC Symbol;Acc:HGNC:9584]","synonyms":"T2R61,PTC","biotype":"protein_coding","ncbi_id":"5726","summary":"This gene encodes a seven-transmembrane G protein-coupled receptor that controls the ability to taste glucosinolates, a family of bitter-tasting compounds found in plants of the Brassica sp. Synthetic compounds phenylthiocarbamide (PTC) and 6-n-propylthiouracil (PROP) have been identified as ligands for this receptor and have been used to test the genetic diversity of this gene. Although several allelic forms of this gene have been identified worldwide, there are two predominant common forms (taster and non-taster) found outside of Africa. These alleles differ at three nucleotide positions resulting in amino acid changes in the protein (A49P, A262V, and V296I) with the amino acid combination PAV identifying the taster variant (and AVI identifying the non-taster variant). [provided by RefSeq, Oct 2009]","start":141972631,"end":141973773,"strand":-1,"description":"taste 2 receptor member 38 [Source:HGNC Symbol;Acc:HGNC:9584]"}, {"versioned_ensembl_gene_id":"ENSG00000166192.14","gene_symbol":"SENP8","gene_name":"SUMO/sentrin peptidase family member, NEDD8 specific [Source:HGNC Symbol;Acc:HGNC:22992]","synonyms":"PRSC2,NEDP1,HsT17512,DEN1","biotype":"protein_coding","ncbi_id":"123228","summary":"This gene encodes a cysteine protease that is a member of the sentrin-specific protease family. The encoded protein is involved in processing and deconjugation of the ubiquitin-like protein termed, neural precursor cell expressed developmentally downregulated 8. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":72114258,"end":72143688,"strand":1,"description":"SUMO/sentrin peptidase family member, NEDD8 specific [Source:HGNC Symbol;Acc:HGNC:22992]"}, {"versioned_ensembl_gene_id":"ENSG00000249545.1","gene_symbol":"AC012312.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94979151,"end":94980893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260600.1","gene_symbol":"AC092125.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":61691756,"end":61693750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237400.1","gene_symbol":"AC006960.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36463023,"end":36504513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065029.14","gene_symbol":"ZNF76","gene_name":"zinc finger protein 76 [Source:HGNC Symbol;Acc:HGNC:13149]","synonyms":"ZNF523,Zfp523,D6S229E","biotype":"protein_coding","ncbi_id":"7629","summary":null,"start":35258909,"end":35295985,"strand":1,"description":"zinc finger protein 76 [Source:HGNC Symbol;Acc:HGNC:13149]"}, {"versioned_ensembl_gene_id":"ENSG00000137767.13","gene_symbol":"SQOR","gene_name":"sulfide quinone oxidoreductase [Source:HGNC Symbol;Acc:HGNC:20390]","synonyms":"SQRDL,SQR,CGI-44","biotype":"protein_coding","ncbi_id":"58472","summary":"The protein encoded by this gene may function in mitochondria to catalyze the conversion of sulfide to persulfides, thereby decreasing toxic concencrations of sulfide. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2012]","start":45631148,"end":45691294,"strand":1,"description":"sulfide quinone oxidoreductase [Source:HGNC Symbol;Acc:HGNC:20390]"}, {"versioned_ensembl_gene_id":"ENSG00000243953.1","gene_symbol":"AC073359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154969283,"end":154970223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227021.1","gene_symbol":"AC007557.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216868012,"end":216869156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256552.2","gene_symbol":"AC092745.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":8320381,"end":8369555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256537.4","gene_symbol":"SMIM10L1","gene_name":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129361","summary":null,"start":11171222,"end":11176016,"strand":1,"description":"small integral membrane protein 10 like 1 [Source:HGNC Symbol;Acc:HGNC:49847]"}, {"versioned_ensembl_gene_id":"ENSG00000233853.1","gene_symbol":"BX927235.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32621417,"end":32623878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282648.1","gene_symbol":"AC243657.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28929748,"end":28933507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239288.1","gene_symbol":"AC063923.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109241507,"end":109243125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283093.1","gene_symbol":"CENPVL2","gene_name":"centromere protein V like 2 [Source:HGNC Symbol;Acc:HGNC:43879]","synonyms":"CENPVP2","biotype":"protein_coding","ncbi_id":"441495","summary":null,"start":51681212,"end":51682831,"strand":-1,"description":"centromere protein V like 2 [Source:HGNC Symbol;Acc:HGNC:43879]"}, {"versioned_ensembl_gene_id":"ENSG00000255413.1","gene_symbol":"AC022880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13741809,"end":13742781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224641.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"AB023051.1,NCRNA00149","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30756658,"end":30782086,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000188038.7","gene_symbol":"NRN1L","gene_name":"neuritin 1 like [Source:HGNC Symbol;Acc:HGNC:29811]","synonyms":"UNQ2446,MRCC2446","biotype":"protein_coding","ncbi_id":"123904","summary":"The protein encoded by this gene is extracellular and enhances both neurite growth and neuronal survival. The encoded protein is found both as a GPI anchored membrane-bound form and as a secreted form. This activity-related ligand functions as a homodimer or heterodimer. [provided by RefSeq, Feb 2017]","start":67884805,"end":67888855,"strand":1,"description":"neuritin 1 like [Source:HGNC Symbol;Acc:HGNC:29811]"}, {"versioned_ensembl_gene_id":"ENSG00000256981.1","gene_symbol":"AC134349.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11158785,"end":11159694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116299.16","gene_symbol":"KIAA1324","gene_name":"KIAA1324 [Source:HGNC Symbol;Acc:HGNC:29618]","synonyms":"EIG121,maba1","biotype":"protein_coding","ncbi_id":"57535","summary":"Expression of this gene is induced by estrogen and the encoded protein has been characterized as a transmembrane protein. The encoded protein has been found in to correlate with survival in certain carcinomas (PMID: 21102415) and may be important for cellular response to stress (PMID: 21072319). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":109113679,"end":109206781,"strand":1,"description":"KIAA1324 [Source:HGNC Symbol;Acc:HGNC:29618]"}, {"versioned_ensembl_gene_id":"ENSG00000141456.14","gene_symbol":"PELP1","gene_name":"proline, glutamate and leucine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:30134]","synonyms":"MNAR","biotype":"protein_coding","ncbi_id":"27043","summary":"This gene encodes a transcription factor which coactivates transcription of estrogen receptor responsive genes and corepresses genes activated by other hormone receptors or sequence-specific transcription factors. Expression of this gene is regulated by both members of the estrogen receptor family. This gene may be involved in the progression of several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":4669774,"end":4704337,"strand":-1,"description":"proline, glutamate and leucine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:30134]"}, {"versioned_ensembl_gene_id":"ENSG00000236386.1","gene_symbol":"AC009518.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131893822,"end":131894074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255179.1","gene_symbol":"AC027804.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7222933,"end":7230863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283659.1","gene_symbol":"AC006453.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89666033,"end":89683204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213683.4","gene_symbol":"AC002056.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50754675,"end":50755434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013573.16","gene_symbol":"DDX11","gene_name":"DEAD/H-box helicase 11 [Source:HGNC Symbol;Acc:HGNC:2736]","synonyms":"WABS,KRG2,CHLR1,CHL1","biotype":"protein_coding","ncbi_id":"1663","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an enzyme that possesses both ATPase and DNA helicase activities. This gene is a homolog of the yeast CHL1 gene, and may function to maintain chromosome transmission fidelity and genome stability. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":31073845,"end":31104791,"strand":1,"description":"DEAD/H-box helicase 11 [Source:HGNC Symbol;Acc:HGNC:2736]"}, {"versioned_ensembl_gene_id":"ENSG00000171681.12","gene_symbol":"ATF7IP","gene_name":"activating transcription factor 7 interacting protein [Source:HGNC Symbol;Acc:HGNC:20092]","synonyms":"p621,FLJ10688","biotype":"protein_coding","ncbi_id":"55729","summary":"ATF7IP is a multifunctional nuclear protein that associates with heterochromatin. It can act as a transcriptional coactivator or corepressor depending upon its binding partners (summary by Liu et al., 2009 [PubMed 19106100]).[supplied by OMIM, Nov 2010]","start":14365632,"end":14502935,"strand":1,"description":"activating transcription factor 7 interacting protein [Source:HGNC Symbol;Acc:HGNC:20092]"}, {"versioned_ensembl_gene_id":"ENSG00000101856.9","gene_symbol":"PGRMC1","gene_name":"progesterone receptor membrane component 1 [Source:HGNC Symbol;Acc:HGNC:16090]","synonyms":"HPR6.6","biotype":"protein_coding","ncbi_id":"10857","summary":"This gene encodes a putative membrane-associated progesterone steroid receptor. The protein is expressed predominantly in the liver and kidney. [provided by RefSeq, Mar 2010]","start":119236245,"end":119244466,"strand":1,"description":"progesterone receptor membrane component 1 [Source:HGNC Symbol;Acc:HGNC:16090]"}, {"versioned_ensembl_gene_id":"ENSG00000236965.4","gene_symbol":"OR52N3P","gene_name":"olfactory receptor family 52 subfamily N member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15229]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"81251","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5800364,"end":5801297,"strand":1,"description":"olfactory receptor family 52 subfamily N member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15229]"}, {"versioned_ensembl_gene_id":"ENSG00000215909.3","gene_symbol":"BRWD1P1","gene_name":"bromodomain and WD repeat domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51528]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481724","summary":null,"start":13555001,"end":13555694,"strand":1,"description":"bromodomain and WD repeat domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51528]"}, {"versioned_ensembl_gene_id":"ENSG00000282476.1","gene_symbol":"IGHV3-20","gene_name":"immunoglobulin heavy variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5585]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28445","summary":null,"start":106211707,"end":106212224,"strand":-1,"description":"immunoglobulin heavy variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5585]"}, {"versioned_ensembl_gene_id":"ENSG00000259961.1","gene_symbol":"AL354712.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13513220,"end":13516270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103226.17","gene_symbol":"NOMO3","gene_name":"NODAL modulator 3 [Source:HGNC Symbol;Acc:HGNC:25242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"408050","summary":"This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a duplicated region on the short arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum. [provided by RefSeq, Jul 2008]","start":16232495,"end":16294814,"strand":1,"description":"NODAL modulator 3 [Source:HGNC Symbol;Acc:HGNC:25242]"}, {"versioned_ensembl_gene_id":"ENSG00000095464.9","gene_symbol":"PDE6C","gene_name":"phosphodiesterase 6C [Source:HGNC Symbol;Acc:HGNC:8787]","synonyms":"PDEA2,COD4,ACHM5","biotype":"protein_coding","ncbi_id":"5146","summary":"This gene encodes the alpha-prime subunit of cone phosphodiesterase, which is composed of a homodimer of two alpha-prime subunits and 3 smaller proteins of 11, 13, and 15 kDa. Mutations in this gene are associated with cone dystrophy type 4 (COD4). [provided by RefSeq, Mar 2010]","start":93612588,"end":93666010,"strand":1,"description":"phosphodiesterase 6C [Source:HGNC Symbol;Acc:HGNC:8787]"}, {"versioned_ensembl_gene_id":"ENSG00000223355.5","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32271266,"end":32300513,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000136048.13","gene_symbol":"DRAM1","gene_name":"DNA damage regulated autophagy modulator 1 [Source:HGNC Symbol;Acc:HGNC:25645]","synonyms":"FLJ11259,DRAM","biotype":"protein_coding","ncbi_id":"55332","summary":"This gene is regulated as part of the p53 tumor suppressor pathway. The gene encodes a lysosomal membrane protein that is required for the induction of autophagy by the pathway. Decreased transcriptional expression of this gene is associated with various tumors. This gene has a pseudogene on chromosome 4. [provided by RefSeq, Jul 2008]","start":101877351,"end":102012130,"strand":1,"description":"DNA damage regulated autophagy modulator 1 [Source:HGNC Symbol;Acc:HGNC:25645]"}, {"versioned_ensembl_gene_id":"ENSG00000257202.1","gene_symbol":"AC084398.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101923410,"end":101924719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224545.1","gene_symbol":"AC008264.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131520137,"end":131520503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279164.1","gene_symbol":"AL118508.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23148086,"end":23149939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232203.3","gene_symbol":"SLC25A6P2","gene_name":"solute carrier family 25 member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43850]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"138412","summary":null,"start":31253901,"end":31254777,"strand":1,"description":"solute carrier family 25 member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43850]"}, {"versioned_ensembl_gene_id":"ENSG00000116266.10","gene_symbol":"STXBP3","gene_name":"syntaxin binding protein 3 [Source:HGNC Symbol;Acc:HGNC:11446]","synonyms":"UNC-18C","biotype":"protein_coding","ncbi_id":"6814","summary":null,"start":108746674,"end":108809526,"strand":1,"description":"syntaxin binding protein 3 [Source:HGNC Symbol;Acc:HGNC:11446]"}, {"versioned_ensembl_gene_id":"ENSG00000228789.6","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"lincRNA","ncbi_id":"285834","summary":null,"start":31053450,"end":31059890,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000237093.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31048998,"end":31054791,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000251484.3","gene_symbol":"AL356488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109103535,"end":109104766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270066.3","gene_symbol":"AL356488.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109100193,"end":109100619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282631.1","gene_symbol":"IGHVII-15-1","gene_name":"immunoglobulin heavy variable (II)-15-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5671]","synonyms":"IGHV(II)-15-1","biotype":"IG_V_pseudogene","ncbi_id":"28376","summary":null,"start":106164354,"end":106164573,"strand":-1,"description":"immunoglobulin heavy variable (II)-15-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5671]"}, {"versioned_ensembl_gene_id":"ENSG00000228301.1","gene_symbol":"RPL7P55","gene_name":"ribosomal protein L7 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36105]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271147","summary":null,"start":93573834,"end":93574579,"strand":1,"description":"ribosomal protein L7 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36105]"}, {"versioned_ensembl_gene_id":"ENSG00000258026.1","gene_symbol":"AC078955.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81094375,"end":81125845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236235.1","gene_symbol":"AP000542.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15290718,"end":15297196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267626.1","gene_symbol":"AC002115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35608285,"end":35612666,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281896.1","gene_symbol":"AC018638.8","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128617865,"end":128625905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138207.13","gene_symbol":"RBP4","gene_name":"retinol binding protein 4 [Source:HGNC Symbol;Acc:HGNC:9922]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5950","summary":" This protein belongs to the lipocalin family and is the specific carrier for retinol (vitamin A alcohol) in the blood. It delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin which prevents its loss by filtration through the kidney glomeruli. A deficiency of vitamin A blocks secretion of the binding protein posttranslationally and results in defective delivery and supply to the epidermal cells. [provided by RefSeq, Jul 2008]","start":93591687,"end":93601744,"strand":-1,"description":"retinol binding protein 4 [Source:HGNC Symbol;Acc:HGNC:9922]"}, {"versioned_ensembl_gene_id":"ENSG00000242588.5","gene_symbol":"AC108010.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":128574751,"end":128622694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278008.1","gene_symbol":"PPP1R26P4","gene_name":"protein phosphatase 1 regulatory subunit 26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42018]","synonyms":"KIAA0649P4","biotype":"processed_pseudogene","ncbi_id":"100132295","summary":null,"start":18715815,"end":18719341,"strand":1,"description":"protein phosphatase 1 regulatory subunit 26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42018]"}, {"versioned_ensembl_gene_id":"ENSG00000233416.1","gene_symbol":"AC012065.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20606280,"end":20606654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138180.15","gene_symbol":"CEP55","gene_name":"centrosomal protein 55 [Source:HGNC Symbol;Acc:HGNC:1161]","synonyms":"FLJ10540,CT111,C10orf3","biotype":"protein_coding","ncbi_id":"55165","summary":null,"start":93496632,"end":93529092,"strand":1,"description":"centrosomal protein 55 [Source:HGNC Symbol;Acc:HGNC:1161]"}, {"versioned_ensembl_gene_id":"ENSG00000242968.1","gene_symbol":"AC096992.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136808551,"end":136809623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261758.1","gene_symbol":"AC117382.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136752630,"end":136755780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235030.3","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30735460,"end":30736815,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000278174.3","gene_symbol":"NSF","gene_name":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]","synonyms":"SKD2,SEC18","biotype":"protein_coding","ncbi_id":"4905","summary":null,"start":46886236,"end":47052838,"strand":1,"description":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]"}, {"versioned_ensembl_gene_id":"ENSG00000282388.1","gene_symbol":"AC024940.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31254265,"end":31254870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233733.1","gene_symbol":"H2AFZP6","gene_name":"H2A histone family member Z pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38019]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462800","summary":null,"start":31521199,"end":31521592,"strand":-1,"description":"H2A histone family member Z pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38019]"}, {"versioned_ensembl_gene_id":"ENSG00000283221.1","gene_symbol":"AC007218.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9794637,"end":9805571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110315.6","gene_symbol":"RNF141","gene_name":"ring finger protein 141 [Source:HGNC Symbol;Acc:HGNC:21159]","synonyms":"ZNF230,ZFP26","biotype":"protein_coding","ncbi_id":"50862","summary":"The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. Abundant expression of this gene was found in the testicular tissue of fertile men, but was not detected in azoospermic patients. Studies of the mouse counterpart suggest that this gene may function as a testis specific transcription factor during spermatogenesis. [provided by RefSeq, Jul 2008]","start":10511678,"end":10541230,"strand":-1,"description":"ring finger protein 141 [Source:HGNC Symbol;Acc:HGNC:21159]"}, {"versioned_ensembl_gene_id":"ENSG00000279973.2","gene_symbol":"CU104787.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11066418,"end":11068174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224910.1","gene_symbol":"LINC01766","gene_name":"long intergenic non-protein coding RNA 1766 [Source:HGNC Symbol;Acc:HGNC:52556]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723617","summary":null,"start":35597907,"end":35601501,"strand":1,"description":"long intergenic non-protein coding RNA 1766 [Source:HGNC Symbol;Acc:HGNC:52556]"}, {"versioned_ensembl_gene_id":"ENSG00000179412.10","gene_symbol":"HNRNPCL4","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060301","summary":null,"start":13164586,"end":13165467,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]"}, {"versioned_ensembl_gene_id":"ENSG00000226243.1","gene_symbol":"RPL37AP1","gene_name":"ribosomal protein L37a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16548]","synonyms":"dJ1013A22.4","biotype":"processed_pseudogene","ncbi_id":"140717","summary":null,"start":44466564,"end":44466842,"strand":-1,"description":"ribosomal protein L37a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16548]"}, {"versioned_ensembl_gene_id":"ENSG00000212856.5","gene_symbol":"TTTY2B","gene_name":"testis-specific transcript, Y-linked 2B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37982]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100101117","summary":null,"start":6406244,"end":6424145,"strand":-1,"description":"testis-specific transcript, Y-linked 2B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37982]"}, {"versioned_ensembl_gene_id":"ENSG00000261212.1","gene_symbol":"AC234778.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141173235,"end":141173588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253860.1","gene_symbol":"IGKV3-34","gene_name":"immunoglobulin kappa variable 3-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5820]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28909","summary":null,"start":89275298,"end":89275787,"strand":-1,"description":"immunoglobulin kappa variable 3-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5820]"}, {"versioned_ensembl_gene_id":"ENSG00000122862.4","gene_symbol":"SRGN","gene_name":"serglycin [Source:HGNC Symbol;Acc:HGNC:9361]","synonyms":"PRG1,PRG,PPG","biotype":"protein_coding","ncbi_id":"5552","summary":"This gene encodes a protein best known as a hematopoietic cell granule proteoglycan. Proteoglycans stored in the secretory granules of many hematopoietic cells also contain a protease-resistant peptide core, which may be important for neutralizing hydrolytic enzymes. This encoded protein was found to be associated with the macromolecular complex of granzymes and perforin, which may serve as a mediator of granule-mediated apoptosis. Two transcript variants, only one of them protein-coding, have been found for this gene. [provided by RefSeq, Jul 2010]","start":69088106,"end":69104811,"strand":1,"description":"serglycin [Source:HGNC Symbol;Acc:HGNC:9361]"}, {"versioned_ensembl_gene_id":"ENSG00000243663.1","gene_symbol":"RPS4XP14","gene_name":"ribosomal protein S4X pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36737]","synonyms":"RPS4P14","biotype":"processed_pseudogene","ncbi_id":"729097","summary":null,"start":1757231,"end":1758011,"strand":-1,"description":"ribosomal protein S4X pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36737]"}, {"versioned_ensembl_gene_id":"ENSG00000228815.1","gene_symbol":"MARK2P13","gene_name":"microtubule affinity regulating kinase 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39804]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631260","summary":null,"start":36109024,"end":36110872,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39804]"}, {"versioned_ensembl_gene_id":"ENSG00000204684.3","gene_symbol":"AL133464.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22371216,"end":22471557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205745.2","gene_symbol":"AC083864.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36079084,"end":36085736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171155.7","gene_symbol":"C1GALT1C1","gene_name":"C1GALT1 specific chaperone 1 [Source:HGNC Symbol;Acc:HGNC:24338]","synonyms":"COSMC,C1GALT2","biotype":"protein_coding","ncbi_id":"29071","summary":"This gene encodes a type II transmembrane protein that is similar to the core 1 beta1,3-galactosyltransferase 1, which catalyzes the synthesis of the core-1 structure, also known as Thomsen-Friedenreich antigen, on O-linked glycans. This gene product lacks the galactosyltransferase activity itself, but instead acts as a molecular chaperone required for the folding, stability and full activity of the core 1 beta1,3-galactosyltransferase 1. Mutations in this gene have been associated with Tn syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2009]","start":120625793,"end":120630150,"strand":-1,"description":"C1GALT1 specific chaperone 1 [Source:HGNC Symbol;Acc:HGNC:24338]"}, {"versioned_ensembl_gene_id":"ENSG00000250781.1","gene_symbol":"AC024022.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42281830,"end":42391268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236692.2","gene_symbol":"AC099654.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57187892,"end":57189437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248672.5","gene_symbol":"LY75-CD302","gene_name":"LY75-CD302 readthrough [Source:HGNC Symbol;Acc:HGNC:38828]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526664","summary":"This locus represents naturally occurring read-through transcription between the neighboring lymphocyte antigen 75 (LY75) and CD302 molecule (CD302) genes. Alternative splicing results in multiple transcript variants encoding fusion products that share sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":159771851,"end":159904710,"strand":-1,"description":"LY75-CD302 readthrough [Source:HGNC Symbol;Acc:HGNC:38828]"}, {"versioned_ensembl_gene_id":"ENSG00000261051.1","gene_symbol":"AC107021.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":146059585,"end":146061679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270629.5","gene_symbol":"NBPF14","gene_name":"NBPF member 14 [Source:HGNC Symbol;Acc:HGNC:25232]","synonyms":"DJ328E19.C1.1","biotype":"protein_coding","ncbi_id":"25832","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013]","start":148531385,"end":148679751,"strand":-1,"description":"NBPF member 14 [Source:HGNC Symbol;Acc:HGNC:25232]"}, {"versioned_ensembl_gene_id":"ENSG00000142347.16","gene_symbol":"MYO1F","gene_name":"myosin IF [Source:HGNC Symbol;Acc:HGNC:7600]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4542","summary":"Myosins are molecular motors that use the energy from ATP hydrolysis to generate force on actin filaments. The protein encoded by this gene is an unconventional myosin that may be involved in the intracellular movement of membrane-enclosed compartments. There is evidence to suggest that mutations in this gene can result in hearing loss. [provided by RefSeq, Jan 2017]","start":8520790,"end":8577577,"strand":-1,"description":"myosin IF [Source:HGNC Symbol;Acc:HGNC:7600]"}, {"versioned_ensembl_gene_id":"ENSG00000251285.2","gene_symbol":"AC097484.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88220569,"end":88223837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235857.1","gene_symbol":"CTBP2P1","gene_name":"C-terminal binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"352905","summary":null,"start":56855244,"end":56855488,"strand":1,"description":"C-terminal binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23940]"}, {"versioned_ensembl_gene_id":"ENSG00000284474.1","gene_symbol":"AC099654.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57167039,"end":57167245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274328.1","gene_symbol":"AC007551.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35847038,"end":35847426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117543.20","gene_symbol":"DPH5","gene_name":"diphthamide biosynthesis 5 [Source:HGNC Symbol;Acc:HGNC:24270]","synonyms":"CGI-30","biotype":"protein_coding","ncbi_id":"51611","summary":"This gene encodes a component of the diphthamide synthesis pathway. Diphthamide is a post-translationally modified histidine residue found only on translation elongation factor 2. It is conserved from archaebacteria to humans, and is targeted by diphtheria toxin and Pseudomonas exotoxin A to halt cellular protein synthesis. The yeast and Chinese hamster homologs of this protein catalyze the trimethylation of the histidine residue on elongation factor 2, resulting in a diphthine moiety that is subsequently amidated to yield diphthamide. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":100989623,"end":101026088,"strand":-1,"description":"diphthamide biosynthesis 5 [Source:HGNC Symbol;Acc:HGNC:24270]"}, {"versioned_ensembl_gene_id":"ENSG00000232682.2","gene_symbol":"AL592430.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60050668,"end":60060743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282121.1","gene_symbol":"AL592430.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60139912,"end":60140877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261994.5","gene_symbol":"WEE2-AS1","gene_name":"WEE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48669]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285962","summary":null,"start":141710346,"end":141744354,"strand":-1,"description":"WEE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48669]"}, {"versioned_ensembl_gene_id":"ENSG00000134697.12","gene_symbol":"GNL2","gene_name":"G protein nucleolar 2 [Source:HGNC Symbol;Acc:HGNC:29925]","synonyms":"Nug2,Nog2,Ngp-1,HUMAUANTIG","biotype":"protein_coding","ncbi_id":"29889","summary":null,"start":37566816,"end":37595935,"strand":-1,"description":"G protein nucleolar 2 [Source:HGNC Symbol;Acc:HGNC:29925]"}, {"versioned_ensembl_gene_id":"ENSG00000267391.4","gene_symbol":"AC105105.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58446275,"end":58453766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158869.10","gene_symbol":"FCER1G","gene_name":"Fc fragment of IgE receptor Ig [Source:HGNC Symbol;Acc:HGNC:3611]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2207","summary":"The high affinity IgE receptor is a key molecule involved in allergic reactions. It is a tetramer composed of 1 alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. [provided by RefSeq, Jul 2008]","start":161215234,"end":161220699,"strand":1,"description":"Fc fragment of IgE receptor Ig [Source:HGNC Symbol;Acc:HGNC:3611]"}, {"versioned_ensembl_gene_id":"ENSG00000223445.1","gene_symbol":"RPL6P21","gene_name":"ribosomal protein L6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270846","summary":null,"start":14070535,"end":14071380,"strand":-1,"description":"ribosomal protein L6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35994]"}, {"versioned_ensembl_gene_id":"ENSG00000160801.13","gene_symbol":"PTH1R","gene_name":"parathyroid hormone 1 receptor [Source:HGNC Symbol;Acc:HGNC:9608]","synonyms":"PTHR1,PTHR","biotype":"protein_coding","ncbi_id":"5745","summary":"The protein encoded by this gene is a member of the G-protein coupled receptor family 2. This protein is a receptor for parathyroid hormone (PTH) and for parathyroid hormone-like hormone (PTHLH). The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system. Defects in this receptor are known to be the cause of Jansen's metaphyseal chondrodysplasia (JMC), chondrodysplasia Blomstrand type (BOCD), as well as enchodromatosis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]","start":46877746,"end":46903799,"strand":1,"description":"parathyroid hormone 1 receptor [Source:HGNC Symbol;Acc:HGNC:9608]"}, {"versioned_ensembl_gene_id":"ENSG00000274336.2","gene_symbol":"CDIP1","gene_name":"cell death inducing p53 target 1 [Source:HGNC Symbol;Acc:HGNC:13234]","synonyms":"LITAFL,CDIP,C16orf5","biotype":"protein_coding","ncbi_id":"29965","summary":null,"start":4512634,"end":4526261,"strand":-1,"description":"cell death inducing p53 target 1 [Source:HGNC Symbol;Acc:HGNC:13234]"}, {"versioned_ensembl_gene_id":"ENSG00000126522.16","gene_symbol":"ASL","gene_name":"argininosuccinate lyase [Source:HGNC Symbol;Acc:HGNC:746]","synonyms":null,"biotype":"protein_coding","ncbi_id":"435","summary":"This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":66075798,"end":66093558,"strand":1,"description":"argininosuccinate lyase [Source:HGNC Symbol;Acc:HGNC:746]"}, {"versioned_ensembl_gene_id":"ENSG00000234185.2","gene_symbol":"AC068533.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66119603,"end":66165011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023839.10","gene_symbol":"ABCC2","gene_name":"ATP binding cassette subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:53]","synonyms":"MRP2,DJS,cMRP,CMOAT","biotype":"protein_coding","ncbi_id":"1244","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008]","start":99782732,"end":99852192,"strand":1,"description":"ATP binding cassette subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:53]"}, {"versioned_ensembl_gene_id":"ENSG00000153904.18","gene_symbol":"DDAH1","gene_name":"dimethylarginine dimethylaminohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:2715]","synonyms":"DDAH","biotype":"protein_coding","ncbi_id":"23576","summary":"This gene belongs to the dimethylarginine dimethylaminohydrolase (DDAH) gene family. The encoded enzyme plays a role in nitric oxide generation by regulating cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. [provided by RefSeq, Jul 2008]","start":85318481,"end":85578363,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:2715]"}, {"versioned_ensembl_gene_id":"ENSG00000225714.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"POLR2LP,AB023060.6","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31185651,"end":31185837,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000001629.9","gene_symbol":"ANKIB1","gene_name":"ankyrin repeat and IBR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22215]","synonyms":"KIAA1386,DKFZP434A0225","biotype":"protein_coding","ncbi_id":"54467","summary":null,"start":92246234,"end":92401384,"strand":1,"description":"ankyrin repeat and IBR domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22215]"}, {"versioned_ensembl_gene_id":"ENSG00000282578.1","gene_symbol":"IGHD2-2","gene_name":"immunoglobulin heavy diversity 2-2 [Source:HGNC Symbol;Acc:HGNC:5490]","synonyms":"IGHD22","biotype":"IG_D_gene","ncbi_id":"28505","summary":null,"start":105917597,"end":105917627,"strand":-1,"description":"immunoglobulin heavy diversity 2-2 [Source:HGNC Symbol;Acc:HGNC:5490]"}, {"versioned_ensembl_gene_id":"ENSG00000282754.1","gene_symbol":"IGHD3-3","gene_name":"immunoglobulin heavy diversity 3-3 [Source:HGNC Symbol;Acc:HGNC:5498]","synonyms":"IGHD33,DXP4","biotype":"IG_D_gene","ncbi_id":"28501","summary":"IGHD3-3 belongs to a cluster of approximately 25 functional diversity (D) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the D gene cluster, see (MIM 146910).[supplied by OMIM, Apr 2008]","start":105915130,"end":105915160,"strand":-1,"description":"immunoglobulin heavy diversity 3-3 [Source:HGNC Symbol;Acc:HGNC:5498]"}, {"versioned_ensembl_gene_id":"ENSG00000282227.1","gene_symbol":"IGHD4-4","gene_name":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]","synonyms":"IGHD44,DA4","biotype":"IG_D_gene","ncbi_id":"28496","summary":null,"start":105913993,"end":105914008,"strand":-1,"description":"immunoglobulin heavy diversity 4-4 [Source:HGNC Symbol;Acc:HGNC:5505]"}, {"versioned_ensembl_gene_id":"ENSG00000229488.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32187767,"end":32193781,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000258477.1","gene_symbol":"PPIAP6","gene_name":"peptidylprolyl isomerase A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:20028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319128","summary":null,"start":68421698,"end":68422196,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:20028]"}, {"versioned_ensembl_gene_id":"ENSG00000235336.8","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31930215,"end":31946068,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000224315.2","gene_symbol":"RPL7P7","gene_name":"ribosomal protein L7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36895]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644896","summary":null,"start":8786211,"end":8786913,"strand":-1,"description":"ribosomal protein L7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36895]"}, {"versioned_ensembl_gene_id":"ENSG00000145623.12","gene_symbol":"OSMR","gene_name":"oncostatin M receptor [Source:HGNC Symbol;Acc:HGNC:8507]","synonyms":"OSMRB","biotype":"protein_coding","ncbi_id":"9180","summary":"This gene encodes a member of the type I cytokine receptor family. The encoded protein heterodimerizes with interleukin 6 signal transducer to form the type II oncostatin M receptor and with interleukin 31 receptor A to form the interleukin 31 receptor, and thus transduces oncostatin M and interleukin 31 induced signaling events. Mutations in this gene have been associated with familial primary localized cutaneous amyloidosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":38845858,"end":38945596,"strand":1,"description":"oncostatin M receptor [Source:HGNC Symbol;Acc:HGNC:8507]"}, {"versioned_ensembl_gene_id":"ENSG00000165102.14","gene_symbol":"HGSNAT","gene_name":"heparan-alpha-glucosaminide N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:26527]","synonyms":"TMEM76,HGNAT,FLJ32731","biotype":"protein_coding","ncbi_id":"138050","summary":"This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. [provided by RefSeq, Jan 2009]","start":43140455,"end":43202855,"strand":1,"description":"heparan-alpha-glucosaminide N-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:26527]"}, {"versioned_ensembl_gene_id":"ENSG00000270282.1","gene_symbol":"AL096855.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8512653,"end":8513021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177666.16","gene_symbol":"PNPLA2","gene_name":"patatin like phospholipase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30802]","synonyms":"TTS-2.2,iPLA2zeta,FP17548,desnutrin,ATGL","biotype":"protein_coding","ncbi_id":"57104","summary":"This gene encodes an enzyme which catalyzes the first step in the hydrolysis of triglycerides in adipose tissue. Mutations in this gene are associated with neutral lipid storage disease with myopathy. [provided by RefSeq, Jul 2010]","start":818902,"end":825573,"strand":1,"description":"patatin like phospholipase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30802]"}, {"versioned_ensembl_gene_id":"ENSG00000240281.2","gene_symbol":"AC034222.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41895068,"end":41895599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204386.10","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31857659,"end":31862906,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000137601.16","gene_symbol":"NEK1","gene_name":"NIMA related kinase 1 [Source:HGNC Symbol;Acc:HGNC:7744]","synonyms":"KIAA1901,NY-REN-55","biotype":"protein_coding","ncbi_id":"4750","summary":"The protein encoded by this gene is a serine/threonine kinase involved in cell cycle regulation. The encoded protein is found in a centrosomal complex with FEZ1, a neuronal protein that plays a role in axonal development. Defects in this gene are a cause of polycystic kidney disease (PKD). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":169392857,"end":169612629,"strand":-1,"description":"NIMA related kinase 1 [Source:HGNC Symbol;Acc:HGNC:7744]"}, {"versioned_ensembl_gene_id":"ENSG00000236710.1","gene_symbol":"AC108448.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3084393,"end":3085443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284309.1","gene_symbol":"AL391650.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":26046665,"end":26049099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225867.1","gene_symbol":"AL022315.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37550026,"end":37551735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224723.1","gene_symbol":"GUSBP10","gene_name":"glucuronidase, beta pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42324]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642006","summary":null,"start":57177409,"end":57180052,"strand":-1,"description":"glucuronidase, beta pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42324]"}, {"versioned_ensembl_gene_id":"ENSG00000163320.10","gene_symbol":"CGGBP1","gene_name":"CGG triplet repeat binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1888]","synonyms":"p20-CGGBP,CGGBP","biotype":"protein_coding","ncbi_id":"8545","summary":"This gene encodes a CGG repeat-binding protein that primarily localizes to the nucleus. CGG trinucleotide repeats are implicated in many disorders as they often act as transcription- and translation-regulatory elements, can produce hairpin structures which cause DNA replication errors, and form regions prone to chromosomal breakage. CGG repeats are also targets for CpG methylation. In addition to its ability to bind CGG repeats and regulate transcription, this gene is believed to play a role in DNA damage repair and telomere protection. In vitro studies indicate this protein does not bind to methylated CpG sequences. [provided by RefSeq, Jul 2017]","start":88051944,"end":88149885,"strand":-1,"description":"CGG triplet repeat binding protein 1 [Source:HGNC Symbol;Acc:HGNC:1888]"}, {"versioned_ensembl_gene_id":"ENSG00000241535.1","gene_symbol":"CBX5P1","gene_name":"chromobox 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38659]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100151661","summary":null,"start":88095408,"end":88095968,"strand":-1,"description":"chromobox 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38659]"}, {"versioned_ensembl_gene_id":"ENSG00000261636.1","gene_symbol":"LINC02191","gene_name":"long intergenic non-protein coding RNA 2191 [Source:HGNC Symbol;Acc:HGNC:53053]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371146","summary":null,"start":25419814,"end":25424169,"strand":-1,"description":"long intergenic non-protein coding RNA 2191 [Source:HGNC Symbol;Acc:HGNC:53053]"}, {"versioned_ensembl_gene_id":"ENSG00000229667.2","gene_symbol":"UBE2V1P9","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44894]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131981","summary":null,"start":90289536,"end":90289903,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44894]"}, {"versioned_ensembl_gene_id":"ENSG00000273001.1","gene_symbol":"AL731533.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3065424,"end":3066001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234182.1","gene_symbol":"AL731533.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3010531,"end":3013111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257956.1","gene_symbol":"NOP56P3","gene_name":"NOP56 ribonucleoprotein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481967","summary":null,"start":79558782,"end":79559166,"strand":1,"description":"NOP56 ribonucleoprotein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49801]"}, {"versioned_ensembl_gene_id":"ENSG00000231743.1","gene_symbol":"AC026396.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2936021,"end":2936441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257474.5","gene_symbol":"AC027288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79540203,"end":79550535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282674.1","gene_symbol":"IGHD5-24","gene_name":"immunoglobulin heavy diversity 5-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5510]","synonyms":"IGHD524","biotype":"IG_D_gene","ncbi_id":"28489","summary":null,"start":105884674,"end":105884693,"strand":-1,"description":"immunoglobulin heavy diversity 5-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5510]"}, {"versioned_ensembl_gene_id":"ENSG00000282640.1","gene_symbol":"IGHD4-23","gene_name":"immunoglobulin heavy diversity 4-23 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5504]","synonyms":"IGHD423","biotype":"IG_D_gene","ncbi_id":"28493","summary":null,"start":105885641,"end":105885659,"strand":-1,"description":"immunoglobulin heavy diversity 4-23 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5504]"}, {"versioned_ensembl_gene_id":"ENSG00000255091.1","gene_symbol":"AC087442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45651529,"end":45652691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274666.1","gene_symbol":"AL133370.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68113706,"end":68114144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241386.6","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32735083,"end":32739368,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000234170.5","gene_symbol":"AC024908.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2446253,"end":2447352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263684.1","gene_symbol":"AC005209.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11874932,"end":11875828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144406.18","gene_symbol":"UNC80","gene_name":"unc-80 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:26582]","synonyms":"UNC-80,KIAA1843,FLJ33496,C2orf21","biotype":"protein_coding","ncbi_id":"285175","summary":"The protein encoded by this gene is a component of a voltage-independent 'leak' ion-channel complex, in which it performs essential functions, such as serving as a bridge between two other components (sodium leak channel non-selective and UNC79) and as a scaffold for Src kinases. Leak channels play an importnat role in establishment and maintenance of resting membrane potentials in neurons. Mutations in this gene are associated with congenital infantile encephalopathy, intellectual disability and growth issues. [provided by RefSeq, Aug 2016]","start":209771993,"end":209999300,"strand":1,"description":"unc-80 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:26582]"}, {"versioned_ensembl_gene_id":"ENSG00000234997.1","gene_symbol":"AC016745.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113424495,"end":113425324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229406.1","gene_symbol":"OFD1P4Y","gene_name":"OFD1 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:23876]","synonyms":"OFDYP4,OFD1PY4,OFD1P4","biotype":"unprocessed_pseudogene","ncbi_id":"386688","summary":null,"start":18453150,"end":18472137,"strand":-1,"description":"OFD1 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:23876]"}, {"versioned_ensembl_gene_id":"ENSG00000234226.5","gene_symbol":"NDUFS5P2","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44040]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100286918","summary":null,"start":96584422,"end":96584727,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44040]"}, {"versioned_ensembl_gene_id":"ENSG00000163874.10","gene_symbol":"ZC3H12A","gene_name":"zinc finger CCCH-type containing 12A [Source:HGNC Symbol;Acc:HGNC:26259]","synonyms":"MCPIP1,FLJ23231","biotype":"protein_coding","ncbi_id":"80149","summary":"ZC3H12A is an MCP1 (CCL2; MIM 158105)-induced protein that acts as a transcriptional activator and causes cell death of cardiomyocytes, possibly via induction of genes associated with apoptosis.[supplied by OMIM, Mar 2008]","start":37474552,"end":37484379,"strand":1,"description":"zinc finger CCCH-type containing 12A [Source:HGNC Symbol;Acc:HGNC:26259]"}, {"versioned_ensembl_gene_id":"ENSG00000168899.4","gene_symbol":"VAMP5","gene_name":"vesicle associated membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:12646]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10791","summary":"Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein are the main components of a protein complex involved in the docking and/or fusion of vesicles and cell membranes. The VAMP5 gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family and the SNARE superfamily. This VAMP family member may participate in vesicle trafficking events that are associated with myogenesis. [provided by RefSeq, Jul 2008]","start":85584408,"end":85593412,"strand":1,"description":"vesicle associated membrane protein 5 [Source:HGNC Symbol;Acc:HGNC:12646]"}, {"versioned_ensembl_gene_id":"ENSG00000280647.1","gene_symbol":"AC106795.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177939622,"end":177983334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131788.15","gene_symbol":"PIAS3","gene_name":"protein inhibitor of activated STAT 3 [Source:HGNC Symbol;Acc:HGNC:16861]","synonyms":"ZMIZ5,FLJ14651","biotype":"protein_coding","ncbi_id":"10401","summary":"This gene encodes a member of the PIAS [protein inhibitor of activated STAT (signal transducer and activator of transcription)] family of transcriptional modulators. The protein functions as a SUMO (small ubiquitin-like modifier)-E3 ligase which catalyzes the covalent attachment of a SUMO protein to specific target substrates. It directly binds to several transcription factors and either blocks or enhances their activity. Alternatively spliced transcript variants of this gene have been identified, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":145848522,"end":145859836,"strand":-1,"description":"protein inhibitor of activated STAT 3 [Source:HGNC Symbol;Acc:HGNC:16861]"}, {"versioned_ensembl_gene_id":"ENSG00000253932.1","gene_symbol":"AC019270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13338574,"end":13342754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242879.1","gene_symbol":"AC006335.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6307710,"end":6309587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162695.11","gene_symbol":"SLC30A7","gene_name":"solute carrier family 30 member 7 [Source:HGNC Symbol;Acc:HGNC:19306]","synonyms":"ZnTL2,ZNT7","biotype":"protein_coding","ncbi_id":"148867","summary":"Zinc functions as a cofactor for numerous enzymes, nuclear factors, and hormones and as an intra- and intercellular signal ion. Members of the zinc transporter (ZNT)/SLC30 subfamily of the cation diffusion facilitator family, such as SLC30A7, permit cellular efflux of zinc (Seve et al., 2004 [PubMed 15154973]).[supplied by OMIM, Mar 2008]","start":100896076,"end":100981753,"strand":1,"description":"solute carrier family 30 member 7 [Source:HGNC Symbol;Acc:HGNC:19306]"}, {"versioned_ensembl_gene_id":"ENSG00000276687.1","gene_symbol":"AL356130.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":905445,"end":909006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232834.1","gene_symbol":"AC112492.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27847588,"end":27847939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238235.1","gene_symbol":"TSPY11P","gene_name":"testis specific protein, Y-linked 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:23903]","synonyms":"TSPYP1","biotype":"unprocessed_pseudogene","ncbi_id":"347584","summary":null,"start":6266593,"end":6269275,"strand":1,"description":"testis specific protein, Y-linked 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:23903]"}, {"versioned_ensembl_gene_id":"ENSG00000231987.1","gene_symbol":"LINC01787","gene_name":"long intergenic non-protein coding RNA 1787 [Source:HGNC Symbol;Acc:HGNC:52576]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928241","summary":null,"start":96254069,"end":96374125,"strand":-1,"description":"long intergenic non-protein coding RNA 1787 [Source:HGNC Symbol;Acc:HGNC:52576]"}, {"versioned_ensembl_gene_id":"ENSG00000235781.1","gene_symbol":"AL662800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30516266,"end":30519217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228600.1","gene_symbol":"POLR2CP1","gene_name":"RNA polymerase II subunit C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9190]","synonyms":"POLR2CP","biotype":"processed_pseudogene","ncbi_id":"54038","summary":null,"start":14757588,"end":14758352,"strand":1,"description":"RNA polymerase II subunit C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9190]"}, {"versioned_ensembl_gene_id":"ENSG00000106477.18","gene_symbol":"CEP41","gene_name":"centrosomal protein 41 [Source:HGNC Symbol;Acc:HGNC:12370]","synonyms":"TSGA14,JBTS15,FLJ22445,DKFZp762H1311","biotype":"protein_coding","ncbi_id":"95681","summary":"This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":130393771,"end":130442433,"strand":-1,"description":"centrosomal protein 41 [Source:HGNC Symbol;Acc:HGNC:12370]"}, {"versioned_ensembl_gene_id":"ENSG00000275190.3","gene_symbol":"UGT2B10","gene_name":"UDP glucuronosyltransferase family 2 member B10 [Source:HGNC Symbol;Acc:HGNC:12544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7365","summary":null,"start":68698370,"end":68713573,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B10 [Source:HGNC Symbol;Acc:HGNC:12544]"}, {"versioned_ensembl_gene_id":"ENSG00000229168.4","gene_symbol":"RPL19P20","gene_name":"ribosomal protein L19 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35713]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392451","summary":null,"start":44649129,"end":44649719,"strand":1,"description":"ribosomal protein L19 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35713]"}, {"versioned_ensembl_gene_id":"ENSG00000282475.1","gene_symbol":"AC243660.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28461979,"end":28470930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175264.7","gene_symbol":"CHST1","gene_name":"carbohydrate sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:1969]","synonyms":"C6ST,KSGal6ST","biotype":"protein_coding","ncbi_id":"8534","summary":"This locus encodes a member of the keratin sulfotransferase family of proteins. The encoded enzyme catalyzes the sulfation of the proteoglycan keratin. [provided by RefSeq, Aug 2011]","start":45648877,"end":45665622,"strand":-1,"description":"carbohydrate sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:1969]"}, {"versioned_ensembl_gene_id":"ENSG00000140832.9","gene_symbol":"MARVELD3","gene_name":"MARVEL domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30525]","synonyms":"MRVLDC3","biotype":"protein_coding","ncbi_id":"91862","summary":null,"start":71626161,"end":71642114,"strand":1,"description":"MARVEL domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30525]"}, {"versioned_ensembl_gene_id":"ENSG00000250471.2","gene_symbol":"GMPSP1","gene_name":"guanine monophosphate synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728564","summary":null,"start":8174421,"end":8174999,"strand":1,"description":"guanine monophosphate synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39428]"}, {"versioned_ensembl_gene_id":"ENSG00000279481.1","gene_symbol":"AC104791.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145830456,"end":145832980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260185.1","gene_symbol":"AC009097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71655027,"end":71664212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260593.1","gene_symbol":"AC009097.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71623708,"end":71626816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226913.1","gene_symbol":"BSN-AS2","gene_name":"BSN antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:42445]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132677","summary":null,"start":49549306,"end":49554366,"strand":-1,"description":"BSN antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:42445]"}, {"versioned_ensembl_gene_id":"ENSG00000264727.1","gene_symbol":"AC005725.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11288205,"end":11290811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127995.16","gene_symbol":"CASD1","gene_name":"CAS1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16014]","synonyms":"FLJ21879,FLJ21213,C7orf12","biotype":"protein_coding","ncbi_id":"64921","summary":null,"start":94509219,"end":94557019,"strand":1,"description":"CAS1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16014]"}, {"versioned_ensembl_gene_id":"ENSG00000281578.1","gene_symbol":"MAPT-AS1","gene_name":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128977","summary":null,"start":46202111,"end":46254322,"strand":1,"description":"MAPT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43738]"}, {"versioned_ensembl_gene_id":"ENSG00000225244.3","gene_symbol":"AC069152.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56940341,"end":56944353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267057.5","gene_symbol":"LINC01905","gene_name":"long intergenic non-protein coding RNA 1905 [Source:HGNC Symbol;Acc:HGNC:52724]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724698","summary":null,"start":56042135,"end":56096319,"strand":1,"description":"long intergenic non-protein coding RNA 1905 [Source:HGNC Symbol;Acc:HGNC:52724]"}, {"versioned_ensembl_gene_id":"ENSG00000255575.1","gene_symbol":"AC004812.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120057035,"end":120057180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119042.16","gene_symbol":"SATB2","gene_name":"SATB homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21637]","synonyms":"KIAA1034,FLJ21474","biotype":"protein_coding","ncbi_id":"23314","summary":"This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Feb 2010]","start":199269500,"end":199471266,"strand":-1,"description":"SATB homeobox 2 [Source:HGNC Symbol;Acc:HGNC:21637]"}, {"versioned_ensembl_gene_id":"ENSG00000279072.1","gene_symbol":"AC118758.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56809214,"end":56848800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156466.9","gene_symbol":"GDF6","gene_name":"growth differentiation factor 6 [Source:HGNC Symbol;Acc:HGNC:4221]","synonyms":"SGM1,KFS1,KFS,BMP13","biotype":"protein_coding","ncbi_id":"392255","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. Mutations in this gene are associated with Klippel-Feil syndrome, microphthalmia, and Leber congenital amaurosis. [provided by RefSeq, Sep 2016]","start":96142330,"end":96160792,"strand":-1,"description":"growth differentiation factor 6 [Source:HGNC Symbol;Acc:HGNC:4221]"}, {"versioned_ensembl_gene_id":"ENSG00000173402.11","gene_symbol":"DAG1","gene_name":"dystroglycan 1 [Source:HGNC Symbol;Acc:HGNC:2666]","synonyms":"A3a,156DAG,DAG,AGRNR","biotype":"protein_coding","ncbi_id":"1605","summary":"This gene encodes dystroglycan, a central component of dystrophin-glycoprotein complex that links the extracellular matrix and the cytoskeleton in the skeletal muscle. The encoded preproprotein undergoes O- and N-glycosylation, and proteolytic processing to generate alpha and beta subunits. Certain mutations in this gene are known to cause distinct forms of muscular dystrophy. Alternative splicing results in multiple transcript variants, all encoding the same protein. [provided by RefSeq, Nov 2015]","start":49468703,"end":49535618,"strand":1,"description":"dystroglycan 1 [Source:HGNC Symbol;Acc:HGNC:2666]"}, {"versioned_ensembl_gene_id":"ENSG00000259682.1","gene_symbol":"AC091231.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":64470253,"end":64471364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248415.1","gene_symbol":"GAPDHP61","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:4155]","synonyms":"GAPDL6,GAPDHL6","biotype":"processed_pseudogene","ncbi_id":"729403","summary":null,"start":64528667,"end":64529671,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:4155]"}, {"versioned_ensembl_gene_id":"ENSG00000282524.1","gene_symbol":"AF186192.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144701846,"end":144702417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066557.5","gene_symbol":"LRRC40","gene_name":"leucine rich repeat containing 40 [Source:HGNC Symbol;Acc:HGNC:26004]","synonyms":"FLJ20331","biotype":"protein_coding","ncbi_id":"55631","summary":null,"start":70144805,"end":70205620,"strand":-1,"description":"leucine rich repeat containing 40 [Source:HGNC Symbol;Acc:HGNC:26004]"}, {"versioned_ensembl_gene_id":"ENSG00000260526.1","gene_symbol":"AC109347.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112229561,"end":112231596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160753.15","gene_symbol":"RUSC1","gene_name":"RUN and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17153]","synonyms":"NESCA","biotype":"protein_coding","ncbi_id":"23623","summary":null,"start":155320896,"end":155331114,"strand":1,"description":"RUN and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17153]"}, {"versioned_ensembl_gene_id":"ENSG00000236008.1","gene_symbol":"LINC01814","gene_name":"long intergenic non-protein coding RNA 1814 [Source:HGNC Symbol;Acc:HGNC:52618]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929567","summary":null,"start":8559833,"end":8583792,"strand":-1,"description":"long intergenic non-protein coding RNA 1814 [Source:HGNC Symbol;Acc:HGNC:52618]"}, {"versioned_ensembl_gene_id":"ENSG00000282261.1","gene_symbol":"AC129915.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1021688,"end":1022635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264775.1","gene_symbol":"PPIAP14","gene_name":"peptidylprolyl isomerase A pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:9267]","synonyms":"PPIP4","biotype":"processed_pseudogene","ncbi_id":"5486","summary":null,"start":5002759,"end":5003254,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:9267]"}, {"versioned_ensembl_gene_id":"ENSG00000259223.2","gene_symbol":"AC009654.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60073554,"end":60118320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272817.1","gene_symbol":"AL359198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91908131,"end":91909348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273497.1","gene_symbol":"AL359198.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91896704,"end":91896897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171956.6","gene_symbol":"FOXB1","gene_name":"forkhead box B1 [Source:HGNC Symbol;Acc:HGNC:3799]","synonyms":"HFKH-5,FKH5","biotype":"protein_coding","ncbi_id":"27023","summary":null,"start":60004222,"end":60061730,"strand":1,"description":"forkhead box B1 [Source:HGNC Symbol;Acc:HGNC:3799]"}, {"versioned_ensembl_gene_id":"ENSG00000257319.1","gene_symbol":"AC008127.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45050901,"end":45103107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235610.1","gene_symbol":"AC013448.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":223505476,"end":223510933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082126.17","gene_symbol":"MPP4","gene_name":"membrane palmitoylated protein 4 [Source:HGNC Symbol;Acc:HGNC:13680]","synonyms":"DLG6","biotype":"protein_coding","ncbi_id":"58538","summary":"This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) protein family, with an N-terminal PDZ domain, a central src homology 3 region (SH3), and a C-terminal guanylate kinase-like (GUK) domain. The protein is localized to the outer limiting membrane in the retina, and is thought to function in photoreceptor polarity and the organization of specialized intercellular junctions. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":201644870,"end":201698694,"strand":-1,"description":"membrane palmitoylated protein 4 [Source:HGNC Symbol;Acc:HGNC:13680]"}, {"versioned_ensembl_gene_id":"ENSG00000174950.10","gene_symbol":"CD164L2","gene_name":"CD164 molecule like 2 [Source:HGNC Symbol;Acc:HGNC:32043]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388611","summary":null,"start":27379176,"end":27383380,"strand":-1,"description":"CD164 molecule like 2 [Source:HGNC Symbol;Acc:HGNC:32043]"}, {"versioned_ensembl_gene_id":"ENSG00000211803.2","gene_symbol":"TRAV23DV6","gene_name":"T-cell receptor alpha variable 23/delta variable 6 [Source:HGNC Symbol;Acc:HGNC:12120]","synonyms":"TRAV23/DV6,TCRAV17S1","biotype":"TR_V_gene","ncbi_id":"28660","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22086407,"end":22086961,"strand":1,"description":"T-cell receptor alpha variable 23/delta variable 6 [Source:HGNC Symbol;Acc:HGNC:12120]"}, {"versioned_ensembl_gene_id":"ENSG00000211801.3","gene_symbol":"TRAV21","gene_name":"T-cell receptor alpha variable 21 [Source:HGNC Symbol;Acc:HGNC:12118]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28662","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22052514,"end":22053056,"strand":1,"description":"T-cell receptor alpha variable 21 [Source:HGNC Symbol;Acc:HGNC:12118]"}, {"versioned_ensembl_gene_id":"ENSG00000183833.16","gene_symbol":"MAATS1","gene_name":"MYCBP associated and testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24010]","synonyms":"C3orf15,AAT1alpha,AAT1,SPATA26,CaM-IP2","biotype":"protein_coding","ncbi_id":"89876","summary":null,"start":119703022,"end":119767102,"strand":1,"description":"MYCBP associated and testis expressed 1 [Source:HGNC Symbol;Acc:HGNC:24010]"}, {"versioned_ensembl_gene_id":"ENSG00000115183.14","gene_symbol":"TANC1","gene_name":"tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29364]","synonyms":"ROLSB,KIAA1728","biotype":"protein_coding","ncbi_id":"85461","summary":null,"start":158968671,"end":159232659,"strand":1,"description":"tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:29364]"}, {"versioned_ensembl_gene_id":"ENSG00000213189.5","gene_symbol":"BTF3L4P2","gene_name":"basic transcription factor 3 like 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653189","summary":null,"start":159003975,"end":159004320,"strand":1,"description":"basic transcription factor 3 like 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39646]"}, {"versioned_ensembl_gene_id":"ENSG00000272942.1","gene_symbol":"AL022324.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25434324,"end":25435070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173610.12","gene_symbol":"UGT2A1","gene_name":"UDP glucuronosyltransferase family 2 member A1 complex locus [Source:HGNC Symbol;Acc:HGNC:12542]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10941","summary":"The protein encoded by this gene belongs to the UDP-glycosyltransferase family, members of which catalyze biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This enzyme is expressed in the olfactory neuroepithelium, which lines the posterior nasal cavity and is exposed to a wide range of odorants and airborne toxic compounds. Hence, this protein has been suggested to be involved in clearing lipophilic odorant molecules from the sensory epithelium. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. This gene shares exon structure with the UDP glucuronosyltransferase 2A2 family member, which encodes N-terminally distinct isoforms. [provided by RefSeq, Jul 2014]","start":69588417,"end":69653249,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member A1 complex locus [Source:HGNC Symbol;Acc:HGNC:12542]"}, {"versioned_ensembl_gene_id":"ENSG00000213453.3","gene_symbol":"FTH1P3","gene_name":"ferritin heavy chain 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3990]","synonyms":"FTHL3","biotype":"processed_pseudogene","ncbi_id":"2498","summary":null,"start":27392784,"end":27393367,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3990]"}, {"versioned_ensembl_gene_id":"ENSG00000225488.1","gene_symbol":"AC092447.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56482105,"end":56483295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091317.7","gene_symbol":"CMTM6","gene_name":"CKLF like MARVEL transmembrane domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19177]","synonyms":"FLJ20396,CKLFSF6","biotype":"protein_coding","ncbi_id":"54918","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and transmembrane 4 superfamilies. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 3. This gene is widely expressed in many tissues, but the exact function of the encoded protein is unknown. [provided by RefSeq, Jul 2008]","start":32481312,"end":32503408,"strand":-1,"description":"CKLF like MARVEL transmembrane domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19177]"}, {"versioned_ensembl_gene_id":"ENSG00000272597.1","gene_symbol":"AC063944.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107329430,"end":107329962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255271.1","gene_symbol":"AL137224.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34533014,"end":34557924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225167.1","gene_symbol":"TXNP2","gene_name":"thioredoxin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49482]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171416","summary":null,"start":68514375,"end":68514669,"strand":-1,"description":"thioredoxin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49482]"}, {"versioned_ensembl_gene_id":"ENSG00000091656.15","gene_symbol":"ZFHX4","gene_name":"zinc finger homeobox 4 [Source:HGNC Symbol;Acc:HGNC:30939]","synonyms":"ZFH4,FLJ20980","biotype":"protein_coding","ncbi_id":"79776","summary":null,"start":76681219,"end":76867285,"strand":1,"description":"zinc finger homeobox 4 [Source:HGNC Symbol;Acc:HGNC:30939]"}, {"versioned_ensembl_gene_id":"ENSG00000254300.1","gene_symbol":"LINC01111","gene_name":"long intergenic non-protein coding RNA 1111 [Source:HGNC Symbol;Acc:HGNC:49237]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926978","summary":null,"start":76406654,"end":76524356,"strand":1,"description":"long intergenic non-protein coding RNA 1111 [Source:HGNC Symbol;Acc:HGNC:49237]"}, {"versioned_ensembl_gene_id":"ENSG00000021776.10","gene_symbol":"AQR","gene_name":"aquarius intron-binding spliceosomal factor [Source:HGNC Symbol;Acc:HGNC:29513]","synonyms":"KIAA0560,IBP160,fSAP164","biotype":"protein_coding","ncbi_id":"9716","summary":null,"start":34851782,"end":34969839,"strand":-1,"description":"aquarius intron-binding spliceosomal factor [Source:HGNC Symbol;Acc:HGNC:29513]"}, {"versioned_ensembl_gene_id":"ENSG00000259575.1","gene_symbol":"AC012404.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61211913,"end":61214231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273792.1","gene_symbol":"AC022898.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":60847757,"end":60849068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226080.1","gene_symbol":"AC062028.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11102142,"end":11102997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153551.13","gene_symbol":"CMTM7","gene_name":"CKLF like MARVEL transmembrane domain containing 7 [Source:HGNC Symbol;Acc:HGNC:19178]","synonyms":"FLJ30992,CKLFSF7","biotype":"protein_coding","ncbi_id":"112616","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and transmembrane 4 superfamilies. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 3. This gene acts as a tumor suppressor that regulates G1/S transition in the cell cycle, and epidermal growth factor receptor/protein kinase B signaling during tumor pathogenesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]","start":32391671,"end":32483067,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 7 [Source:HGNC Symbol;Acc:HGNC:19178]"}, {"versioned_ensembl_gene_id":"ENSG00000273143.1","gene_symbol":"AL355512.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110428840,"end":110496204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272267.2","gene_symbol":"AC021242.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9555144,"end":9556520,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271166.1","gene_symbol":"AL671309.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71804283,"end":71804826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226421.1","gene_symbol":"SLC25A5P5","gene_name":"solute carrier family 25 member 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:511]","synonyms":"TCAG_29001,ANTP5","biotype":"processed_pseudogene","ncbi_id":"442525","summary":null,"start":32471513,"end":32472409,"strand":1,"description":"solute carrier family 25 member 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:511]"}, {"versioned_ensembl_gene_id":"ENSG00000254559.1","gene_symbol":"AC069287.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203623,"end":205470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237823.1","gene_symbol":"CDY19P","gene_name":"chromodomain Y-linked 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:23863]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386741","summary":null,"start":25564122,"end":25566033,"strand":-1,"description":"chromodomain Y-linked 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:23863]"}, {"versioned_ensembl_gene_id":"ENSG00000240459.2","gene_symbol":"AC093663.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112116510,"end":112116903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248656.1","gene_symbol":"AC083795.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111640495,"end":111648808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251312.2","gene_symbol":"AC004062.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111063583,"end":111064227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251483.2","gene_symbol":"LYPLA1P2","gene_name":"lysophospholipase I pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391686","summary":null,"start":110945109,"end":110945799,"strand":-1,"description":"lysophospholipase I pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44006]"}, {"versioned_ensembl_gene_id":"ENSG00000146576.12","gene_symbol":"C7orf26","gene_name":"chromosome 7 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:21702]","synonyms":"MGC2718","biotype":"protein_coding","ncbi_id":"79034","summary":null,"start":6590017,"end":6608726,"strand":1,"description":"chromosome 7 open reading frame 26 [Source:HGNC Symbol;Acc:HGNC:21702]"}, {"versioned_ensembl_gene_id":"ENSG00000249519.1","gene_symbol":"LINC01438","gene_name":"long intergenic non-protein coding RNA 1438 [Source:HGNC Symbol;Acc:HGNC:50757]","synonyms":"TCONS_00007593","biotype":"lincRNA","ncbi_id":"106144527","summary":null,"start":110794403,"end":110797344,"strand":1,"description":"long intergenic non-protein coding RNA 1438 [Source:HGNC Symbol;Acc:HGNC:50757]"}, {"versioned_ensembl_gene_id":"ENSG00000101161.7","gene_symbol":"PRPF6","gene_name":"pre-mRNA processing factor 6 [Source:HGNC Symbol;Acc:HGNC:15860]","synonyms":"U5-102K,TOM,SNRNP102,RP60,Prp6,hPrp6,C20orf14,bB152O15.1,ANT-1","biotype":"protein_coding","ncbi_id":"24148","summary":"The protein encoded by this gene appears to be involved in pre-mRNA splicing, possibly acting as a bridging factor between U5 and U4/U6 snRNPs in formation of the spliceosome. The encoded protein also can bind androgen receptor, providing a link between transcriptional activation and splicing. [provided by RefSeq, Jul 2008]","start":63981135,"end":64033100,"strand":1,"description":"pre-mRNA processing factor 6 [Source:HGNC Symbol;Acc:HGNC:15860]"}, {"versioned_ensembl_gene_id":"ENSG00000276531.1","gene_symbol":"AC091769.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72483245,"end":72483812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235583.2","gene_symbol":"AC007562.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25512301,"end":25527786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220201.7","gene_symbol":"ZGLP1","gene_name":"zinc finger, GATA-like protein 1 [Source:HGNC Symbol;Acc:HGNC:37245]","synonyms":"GLP1,GLP-1,GATAD3","biotype":"protein_coding","ncbi_id":"100125288","summary":null,"start":10304803,"end":10309880,"strand":-1,"description":"zinc finger, GATA-like protein 1 [Source:HGNC Symbol;Acc:HGNC:37245]"}, {"versioned_ensembl_gene_id":"ENSG00000259591.1","gene_symbol":"AC022898.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60763906,"end":60765625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170581.13","gene_symbol":"STAT2","gene_name":"signal transducer and activator of transcription 2 [Source:HGNC Symbol;Acc:HGNC:11363]","synonyms":"STAT113","biotype":"protein_coding","ncbi_id":"6773","summary":"The protein encoded by this gene is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. In response to interferon (IFN), this protein forms a complex with STAT1 and IFN regulatory factor family protein p48 (ISGF3G), in which this protein acts as a transactivator, but lacks the ability to bind DNA directly. The protein mediates innate antiviral activity. Mutations in this gene result in Immunodeficiency 44. [provided by RefSeq, Aug 2020]","start":56341597,"end":56360155,"strand":-1,"description":"signal transducer and activator of transcription 2 [Source:HGNC Symbol;Acc:HGNC:11363]"}, {"versioned_ensembl_gene_id":"ENSG00000077092.18","gene_symbol":"RARB","gene_name":"retinoic acid receptor beta [Source:HGNC Symbol;Acc:HGNC:9865]","synonyms":"RRB2,NR1B2,HAP","biotype":"protein_coding","ncbi_id":"5915","summary":"This gene encodes retinoic acid receptor beta, a member of the thyroid-steroid hormone receptor superfamily of nuclear transcriptional regulators. This receptor localizes to the cytoplasm and to subnuclear compartments. It binds retinoic acid, the biologically active form of vitamin A which mediates cellular signalling in embryonic morphogenesis, cell growth and differentiation. It is thought that this protein limits growth of many cell types by regulating gene expression. The gene was first identified in a hepatocellular carcinoma where it flanks a hepatitis B virus integration site. Alternate promoter usage and differential splicing result in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":25174332,"end":25597932,"strand":1,"description":"retinoic acid receptor beta [Source:HGNC Symbol;Acc:HGNC:9865]"}, {"versioned_ensembl_gene_id":"ENSG00000006468.13","gene_symbol":"ETV1","gene_name":"ETS variant 1 [Source:HGNC Symbol;Acc:HGNC:3490]","synonyms":"ER81","biotype":"protein_coding","ncbi_id":"2115","summary":"This gene encodes a member of the ETS (E twenty-six) family of transcription factors. The ETS proteins regulate many target genes that modulate biological processes like cell growth, angiogenesis, migration, proliferation and differentiation. All ETS proteins contain an ETS DNA-binding domain that binds to DNA sequences containing the consensus 5'-CGGA[AT]-3'. The protein encoded by this gene contains a conserved short acidic transactivation domain (TAD) in the N-terminal region, in addition to the ETS DNA-binding domain in the C-terminal region. This gene is involved in chromosomal translocations, which result in multiple fusion proteins including EWS-ETV1 in Ewing sarcoma and at least 10 ETV1 partners (see PMID: 19657377, Table 1) in prostate cancer. In addition to chromosomal rearrangement, this gene is overexpressed in prostate cancer, melanoma and gastrointestinal stromal tumor. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2016]","start":13891228,"end":13991425,"strand":-1,"description":"ETS variant 1 [Source:HGNC Symbol;Acc:HGNC:3490]"}, {"versioned_ensembl_gene_id":"ENSG00000262734.1","gene_symbol":"AC217785.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155211179,"end":155213671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239539.1","gene_symbol":"HMGN1P20","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874459","summary":null,"start":19489101,"end":19489400,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39364]"}, {"versioned_ensembl_gene_id":"ENSG00000138670.17","gene_symbol":"RASGEF1B","gene_name":"RasGEF domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24881]","synonyms":"GPIG4,FLJ31695","biotype":"protein_coding","ncbi_id":"153020","summary":null,"start":81426393,"end":82044244,"strand":-1,"description":"RasGEF domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24881]"}, {"versioned_ensembl_gene_id":"ENSG00000239636.1","gene_symbol":"AC004865.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35569813,"end":35577729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225900.1","gene_symbol":"HSPE1P13","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49332]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480256","summary":null,"start":39098149,"end":39098445,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49332]"}, {"versioned_ensembl_gene_id":"ENSG00000237662.1","gene_symbol":"SOCS2P1","gene_name":"suppressor of cytokine signaling 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"276719","summary":null,"start":33187391,"end":33188292,"strand":1,"description":"suppressor of cytokine signaling 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16069]"}, {"versioned_ensembl_gene_id":"ENSG00000231290.5","gene_symbol":"APCDD1L-AS1","gene_name":"APCDD1L antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27152]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"149773","summary":null,"start":58515379,"end":58619888,"strand":1,"description":"APCDD1L antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27152]"}, {"versioned_ensembl_gene_id":"ENSG00000118965.14","gene_symbol":"WDR35","gene_name":"WD repeat domain 35 [Source:HGNC Symbol;Acc:HGNC:29250]","synonyms":"MGC33196,KIAA1336,IFTA1,IFT121","biotype":"protein_coding","ncbi_id":"57539","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.[provided by RefSeq, Sep 2010]","start":19910260,"end":19990131,"strand":-1,"description":"WD repeat domain 35 [Source:HGNC Symbol;Acc:HGNC:29250]"}, {"versioned_ensembl_gene_id":"ENSG00000064012.21","gene_symbol":"CASP8","gene_name":"caspase 8 [Source:HGNC Symbol;Acc:HGNC:1509]","synonyms":"MCH5,MACH,FLICE,Casp-8","biotype":"protein_coding","ncbi_id":"841","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain, a large protease subunit, and a small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This protein is involved in the programmed cell death induced by Fas and various apoptotic stimuli. The N-terminal FADD-like death effector domain of this protein suggests that it may interact with Fas-interacting protein FADD. This protein was detected in the insoluble fraction of the affected brain region from Huntington disease patients but not in those from normal controls, which implicated the role in neurodegenerative diseases. Many alternatively spliced transcript variants encoding different isoforms have been described, although not all variants have had their full-length sequences determined. [provided by RefSeq, Jul 2008]","start":201233443,"end":201287711,"strand":1,"description":"caspase 8 [Source:HGNC Symbol;Acc:HGNC:1509]"}, {"versioned_ensembl_gene_id":"ENSG00000137434.11","gene_symbol":"C6orf52","gene_name":"chromosome 6 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:20881]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347744","summary":null,"start":10671418,"end":10694797,"strand":-1,"description":"chromosome 6 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:20881]"}, {"versioned_ensembl_gene_id":"ENSG00000278088.4","gene_symbol":"CYP2D7","gene_name":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]","synonyms":"CYP2D7P,CYP2D,CYP2D@,CYP2D7P1","biotype":"polymorphic_pseudogene","ncbi_id":"1564","summary":"This gene is a member of the cytochrome P450 gene superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is a segregating pseudogene, where some individuals may have an allele that encodes a functional enzyme, while other individuals have an allele encoding a protein that is predicted to be non-functional. In this case, the functional allele is thought to be rare. This locus is part of a cluster of cytochrome P450 genes on chromosome 22. [provided by RefSeq, Jan 2017]","start":42140208,"end":42144572,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]"}, {"versioned_ensembl_gene_id":"ENSG00000124575.6","gene_symbol":"HIST1H1D","gene_name":"histone cluster 1 H1 family member d [Source:HGNC Symbol;Acc:HGNC:4717]","synonyms":"H1s-2,H1F3,H1d,H1.3","biotype":"protein_coding","ncbi_id":"3007","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26234268,"end":26234933,"strand":-1,"description":"histone cluster 1 H1 family member d [Source:HGNC Symbol;Acc:HGNC:4717]"}, {"versioned_ensembl_gene_id":"ENSG00000087245.12","gene_symbol":"MMP2","gene_name":"matrix metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:7166]","synonyms":"TBE-1,CLG4A,CLG4","biotype":"protein_coding","ncbi_id":"4313","summary":"This gene is a member of the matrix metalloproteinase (MMP) gene family, that are zinc-dependent enzymes capable of cleaving components of the extracellular matrix and molecules involved in signal transduction. The protein encoded by this gene is a gelatinase A, type IV collagenase, that contains three fibronectin type II repeats in its catalytic site that allow binding of denatured type IV and V collagen and elastin. Unlike most MMP family members, activation of this protein can occur on the cell membrane. This enzyme can be activated extracellularly by proteases, or, intracellulary by its S-glutathiolation with no requirement for proteolytical removal of the pro-domain. This protein is thought to be involved in multiple pathways including roles in the nervous system, endometrial menstrual breakdown, regulation of vascularization, and metastasis. Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":55389700,"end":55506691,"strand":1,"description":"matrix metallopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:7166]"}, {"versioned_ensembl_gene_id":"ENSG00000259962.1","gene_symbol":"AC007342.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53362019,"end":53363678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243646.9","gene_symbol":"IL10RB","gene_name":"interleukin 10 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:5965]","synonyms":"CRF2-4,CDW210B,IL-10R2,D21S66,D21S58,CRFB4","biotype":"protein_coding","ncbi_id":"3588","summary":"The protein encoded by this gene belongs to the cytokine receptor family. It is an accessory chain essential for the active interleukin 10 receptor complex. Coexpression of this and IL10RA proteins has been shown to be required for IL10-induced signal transduction. This gene and three other interferon receptor genes, IFAR2, IFNAR1, and IFNGR2, form a class II cytokine receptor gene cluster located in a small region on chromosome 21. [provided by RefSeq, Jul 2008]","start":33266358,"end":33310187,"strand":1,"description":"interleukin 10 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:5965]"}, {"versioned_ensembl_gene_id":"ENSG00000253859.2","gene_symbol":"AC018616.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81439436,"end":81521818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260135.6","gene_symbol":"MMP2-AS1","gene_name":"MMP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53142]","synonyms":"ENST00000569037","biotype":"lincRNA","ncbi_id":"107984884","summary":null,"start":55426797,"end":55462297,"strand":-1,"description":"MMP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53142]"}, {"versioned_ensembl_gene_id":"ENSG00000279030.1","gene_symbol":"AC007336.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":55486618,"end":55488777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145002.12","gene_symbol":"FAM86B2","gene_name":"family with sequence similarity 86 member B2 [Source:HGNC Symbol;Acc:HGNC:32222]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653333","summary":null,"start":12425614,"end":12436343,"strand":-1,"description":"family with sequence similarity 86 member B2 [Source:HGNC Symbol;Acc:HGNC:32222]"}, {"versioned_ensembl_gene_id":"ENSG00000197852.9","gene_symbol":"FAM212B","gene_name":"family with sequence similarity 212 member B [Source:HGNC Symbol;Acc:HGNC:28045]","synonyms":"INKA2,FLJ31105,C1orf183","biotype":"protein_coding","ncbi_id":"55924","summary":null,"start":111680630,"end":111755824,"strand":-1,"description":"family with sequence similarity 212 member B [Source:HGNC Symbol;Acc:HGNC:28045]"}, {"versioned_ensembl_gene_id":"ENSG00000198088.10","gene_symbol":"NUP62CL","gene_name":"nucleoporin 62 C-terminal like [Source:HGNC Symbol;Acc:HGNC:25960]","synonyms":"FLJ20130","biotype":"protein_coding","ncbi_id":"54830","summary":"This gene encodes a protein containing a domain found in nucleoporins which are glycoproteins found in nuclear pore complexes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":107123427,"end":107206433,"strand":-1,"description":"nucleoporin 62 C-terminal like [Source:HGNC Symbol;Acc:HGNC:25960]"}, {"versioned_ensembl_gene_id":"ENSG00000205629.11","gene_symbol":"LCMT1","gene_name":"leucine carboxyl methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17557]","synonyms":"CGI-68,PPMT1","biotype":"protein_coding","ncbi_id":"51451","summary":"LCMT1 catalyzes the methylation of the carboxyl group of the C-terminal leucine residue (leu309) of the catalytic subunit of protein phosphatase-2A (PPP2CA; MIM 176915) (De Baere et al., 1999 [PubMed 10600115]).[supplied by OMIM, Mar 2008]","start":25111729,"end":25178231,"strand":1,"description":"leucine carboxyl methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17557]"}, {"versioned_ensembl_gene_id":"ENSG00000149476.15","gene_symbol":"TKFC","gene_name":"triokinase and FMN cyclase [Source:HGNC Symbol;Acc:HGNC:24552]","synonyms":"NET45,DKFZP586B1621,DAK","biotype":"protein_coding","ncbi_id":"26007","summary":"This gene is a member of the family of dihydroxyacetone kinases, which have a protein structure distinct from other kinases. The product of this gene phosphorylates dihydroxyacetone, and also catalyzes the formation of riboflavin 4',5'-phosphate (aka cyclin FMN) from FAD. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2017]","start":61333210,"end":61353295,"strand":1,"description":"triokinase and FMN cyclase [Source:HGNC Symbol;Acc:HGNC:24552]"}, {"versioned_ensembl_gene_id":"ENSG00000160211.15","gene_symbol":"G6PD","gene_name":"glucose-6-phosphate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4057]","synonyms":"G6PD1","biotype":"protein_coding","ncbi_id":"2539","summary":"This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":154531391,"end":154547572,"strand":-1,"description":"glucose-6-phosphate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4057]"}, {"versioned_ensembl_gene_id":"ENSG00000143553.10","gene_symbol":"SNAPIN","gene_name":"SNAP associated protein [Source:HGNC Symbol;Acc:HGNC:17145]","synonyms":"SNAPAP,BORCS3,BLOC1S7","biotype":"protein_coding","ncbi_id":"23557","summary":"The protein encoded by this gene is a coiled-coil-forming protein that associates with the SNARE (soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor) complex of proteins and the BLOC-1 (biogenesis of lysosome-related organelles) complex. Biochemical studies have identified additional binding partners. As part of the SNARE complex, it is required for vesicle docking and fusion and regulates neurotransmitter release. The BLOC-1 complex is required for the biogenesis of specialized organelles such as melanosomes and platelet dense granules. Mutations in gene products that form the BLOC-1 complex have been identified in mouse strains that are models of Hermansky-Pudlak syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":153658654,"end":153661830,"strand":1,"description":"SNAP associated protein [Source:HGNC Symbol;Acc:HGNC:17145]"}, {"versioned_ensembl_gene_id":"ENSG00000109133.12","gene_symbol":"TMEM33","gene_name":"transmembrane protein 33 [Source:HGNC Symbol;Acc:HGNC:25541]","synonyms":"FLJ10525","biotype":"protein_coding","ncbi_id":"55161","summary":null,"start":41935120,"end":41960572,"strand":1,"description":"transmembrane protein 33 [Source:HGNC Symbol;Acc:HGNC:25541]"}, {"versioned_ensembl_gene_id":"ENSG00000266928.1","gene_symbol":"AC020905.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28294093,"end":28313500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121207.11","gene_symbol":"LRAT","gene_name":"lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase) [Source:HGNC Symbol;Acc:HGNC:6685]","synonyms":"LCA14","biotype":"protein_coding","ncbi_id":"9227","summary":"The protein encoded by this gene localizes to the endoplasmic reticulum, where it catalyzes the esterification of all-trans-retinol into all-trans-retinyl ester. This reaction is an important step in vitamin A metabolism in the visual system. Mutations in this gene have been associated with early-onset severe retinal dystrophy and Leber congenital amaurosis 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":154626945,"end":154753118,"strand":1,"description":"lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase) [Source:HGNC Symbol;Acc:HGNC:6685]"}, {"versioned_ensembl_gene_id":"ENSG00000282144.2","gene_symbol":"TBC1D3I","gene_name":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724862","summary":null,"start":36254011,"end":36264925,"strand":-1,"description":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]"}, {"versioned_ensembl_gene_id":"ENSG00000168172.8","gene_symbol":"HOOK3","gene_name":"hook microtubule tethering protein 3 [Source:HGNC Symbol;Acc:HGNC:23576]","synonyms":"HK3","biotype":"protein_coding","ncbi_id":"84376","summary":"Hook proteins are cytosolic coiled-coil proteins that contain conserved N-terminal domains, which attach to microtubules, and more divergent C-terminal domains, which mediate binding to organelles. The Drosophila Hook protein is a component of the endocytic compartment.[supplied by OMIM, Apr 2004]","start":42896932,"end":43030539,"strand":1,"description":"hook microtubule tethering protein 3 [Source:HGNC Symbol;Acc:HGNC:23576]"}, {"versioned_ensembl_gene_id":"ENSG00000231133.6","gene_symbol":"HAR1B","gene_name":"highly accelerated region 1B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33118]","synonyms":"NCRNA00065,LINC00065,HAR1R","biotype":"lincRNA","ncbi_id":"768097","summary":null,"start":63095493,"end":63102319,"strand":-1,"description":"highly accelerated region 1B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33118]"}, {"versioned_ensembl_gene_id":"ENSG00000177000.11","gene_symbol":"MTHFR","gene_name":"methylenetetrahydrofolate reductase [Source:HGNC Symbol;Acc:HGNC:7436]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4524","summary":"The protein encoded by this gene catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Genetic variation in this gene influences susceptibility to occlusive vascular disease, neural tube defects, colon cancer and acute leukemia, and mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.[provided by RefSeq, Oct 2009]","start":11785723,"end":11806920,"strand":-1,"description":"methylenetetrahydrofolate reductase [Source:HGNC Symbol;Acc:HGNC:7436]"}, {"versioned_ensembl_gene_id":"ENSG00000173281.4","gene_symbol":"PPP1R3B","gene_name":"protein phosphatase 1 regulatory subunit 3B [Source:HGNC Symbol;Acc:HGNC:14942]","synonyms":"FLJ14005,PPP1R4,GL","biotype":"protein_coding","ncbi_id":"79660","summary":"This gene encodes the catalytic subunit of the serine/theonine phosphatase, protein phosphatase-1. The encoded protein is expressed in liver and skeletal muscle tissue and may be involved in regulating glycogen synthesis in these tissues. This gene may be a involved in type 2 diabetes and maturity-onset diabetes of the young. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Jan 2011]","start":9136255,"end":9151574,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 3B [Source:HGNC Symbol;Acc:HGNC:14942]"}, {"versioned_ensembl_gene_id":"ENSG00000099308.10","gene_symbol":"MAST3","gene_name":"microtubule associated serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:19036]","synonyms":"KIAA0561","biotype":"protein_coding","ncbi_id":"23031","summary":null,"start":18097793,"end":18151692,"strand":1,"description":"microtubule associated serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:19036]"}, {"versioned_ensembl_gene_id":"ENSG00000168505.6","gene_symbol":"GBX2","gene_name":"gastrulation brain homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4186]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2637","summary":null,"start":236165236,"end":236168369,"strand":-1,"description":"gastrulation brain homeobox 2 [Source:HGNC Symbol;Acc:HGNC:4186]"}, {"versioned_ensembl_gene_id":"ENSG00000262671.1","gene_symbol":"AC004918.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":141652381,"end":141656810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227275.1","gene_symbol":"MTND6P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39473]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478947","summary":null,"start":131369785,"end":131370301,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39473]"}, {"versioned_ensembl_gene_id":"ENSG00000111291.8","gene_symbol":"GPRC5D","gene_name":"G protein-coupled receptor class C group 5 member D [Source:HGNC Symbol;Acc:HGNC:13310]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55507","summary":"The protein encoded by this gene is a member of the G protein-coupled receptor family; however, the specific function of this gene has not yet been determined. [provided by RefSeq, Jul 2008]","start":12940775,"end":12952147,"strand":-1,"description":"G protein-coupled receptor class C group 5 member D [Source:HGNC Symbol;Acc:HGNC:13310]"}, {"versioned_ensembl_gene_id":"ENSG00000229672.2","gene_symbol":"AL450322.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3751067,"end":3763226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206178.2","gene_symbol":"HBZP1","gene_name":"hemoglobin subunit zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4836]","synonyms":"HBZP,HBZ2P,HBZ2,HBZ-T2","biotype":"unprocessed_pseudogene","ncbi_id":"3051","summary":null,"start":163122,"end":165156,"strand":1,"description":"hemoglobin subunit zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4836]"}, {"versioned_ensembl_gene_id":"ENSG00000204930.9","gene_symbol":"FAM221B","gene_name":"family with sequence similarity 221 member B [Source:HGNC Symbol;Acc:HGNC:30762]","synonyms":"C9orf128","biotype":"protein_coding","ncbi_id":"392307","summary":null,"start":35816391,"end":35828747,"strand":-1,"description":"family with sequence similarity 221 member B [Source:HGNC Symbol;Acc:HGNC:30762]"}, {"versioned_ensembl_gene_id":"ENSG00000228080.10","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32670593,"end":32703817,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000211784.2","gene_symbol":"TRAV10","gene_name":"T-cell receptor alpha variable 10 [Source:HGNC Symbol;Acc:HGNC:12103]","synonyms":"TCRAV10S1,TCRAV24S1","biotype":"TR_V_gene","ncbi_id":"28676","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21825472,"end":21826075,"strand":1,"description":"T-cell receptor alpha variable 10 [Source:HGNC Symbol;Acc:HGNC:12103]"}, {"versioned_ensembl_gene_id":"ENSG00000236379.2","gene_symbol":"ZNF736P4Y","gene_name":"zinc finger protein 736 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38464]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419735","summary":null,"start":25168599,"end":25169841,"strand":1,"description":"zinc finger protein 736 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38464]"}, {"versioned_ensembl_gene_id":"ENSG00000138495.6","gene_symbol":"COX17","gene_name":"COX17, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2264]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10063","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92% amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13. [provided by RefSeq, Jul 2008]","start":119654513,"end":119677454,"strand":-1,"description":"COX17, cytochrome c oxidase copper chaperone [Source:HGNC Symbol;Acc:HGNC:2264]"}, {"versioned_ensembl_gene_id":"ENSG00000215339.3","gene_symbol":"ZNF705CP","gene_name":"zinc finger protein 705C, pseudogene [Source:HGNC Symbol;Acc:HGNC:32283]","synonyms":"ZNF705C","biotype":"unprocessed_pseudogene","ncbi_id":"389631","summary":null,"start":12356136,"end":12359391,"strand":1,"description":"zinc finger protein 705C, pseudogene [Source:HGNC Symbol;Acc:HGNC:32283]"}, {"versioned_ensembl_gene_id":"ENSG00000237992.2","gene_symbol":"LINC01808","gene_name":"long intergenic non-protein coding RNA 1808 [Source:HGNC Symbol;Acc:HGNC:52611]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373460","summary":null,"start":19468997,"end":19520095,"strand":1,"description":"long intergenic non-protein coding RNA 1808 [Source:HGNC Symbol;Acc:HGNC:52611]"}, {"versioned_ensembl_gene_id":"ENSG00000232439.1","gene_symbol":"RPL18AP7","gene_name":"ribosomal protein L18a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35607]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133038","summary":null,"start":38526802,"end":38527325,"strand":-1,"description":"ribosomal protein L18a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35607]"}, {"versioned_ensembl_gene_id":"ENSG00000006634.7","gene_symbol":"DBF4","gene_name":"DBF4 zinc finger [Source:HGNC Symbol;Acc:HGNC:17364]","synonyms":"ZDBF1,DBF4A,chif,ASK","biotype":"protein_coding","ncbi_id":"10926","summary":null,"start":87876216,"end":87909541,"strand":1,"description":"DBF4 zinc finger [Source:HGNC Symbol;Acc:HGNC:17364]"}, {"versioned_ensembl_gene_id":"ENSG00000186973.10","gene_symbol":"FAM183A","gene_name":"family with sequence similarity 183 member A [Source:HGNC Symbol;Acc:HGNC:34347]","synonyms":"LOC440585,hCG23177","biotype":"protein_coding","ncbi_id":"440585","summary":null,"start":43145153,"end":43156396,"strand":1,"description":"family with sequence similarity 183 member A [Source:HGNC Symbol;Acc:HGNC:34347]"}, {"versioned_ensembl_gene_id":"ENSG00000267939.1","gene_symbol":"AC008946.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8008729,"end":8016025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181977.3","gene_symbol":"PYY3","gene_name":"peptide YY 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31855]","synonyms":"OTTHUMG00000021515","biotype":"processed_pseudogene","ncbi_id":"644059","summary":null,"start":50156159,"end":50156371,"strand":1,"description":"peptide YY 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31855]"}, {"versioned_ensembl_gene_id":"ENSG00000237501.1","gene_symbol":"AC108667.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172830981,"end":172831229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235808.1","gene_symbol":"MYL6P2","gene_name":"myosin light chain 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100431168","summary":null,"start":39488327,"end":39488760,"strand":1,"description":"myosin light chain 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23772]"}, {"versioned_ensembl_gene_id":"ENSG00000240755.1","gene_symbol":"ERLEC1P1","gene_name":"endoplasmic reticulum lectin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288870","summary":null,"start":14143581,"end":14144158,"strand":1,"description":"endoplasmic reticulum lectin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38012]"}, {"versioned_ensembl_gene_id":"ENSG00000226674.8","gene_symbol":"TEX41","gene_name":"testis expressed 41 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48667]","synonyms":"LINC00953,DKFZp686O1327","biotype":"lincRNA","ncbi_id":"401014","summary":null,"start":144667967,"end":145262988,"strand":1,"description":"testis expressed 41 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48667]"}, {"versioned_ensembl_gene_id":"ENSG00000278210.1","gene_symbol":"KRTAP5-1","gene_name":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]","synonyms":"KRTAP5.1,KRN1L","biotype":"protein_coding","ncbi_id":"387264","summary":null,"start":1590052,"end":1590993,"strand":-1,"description":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]"}, {"versioned_ensembl_gene_id":"ENSG00000268516.2","gene_symbol":"AC020915.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58257270,"end":58278808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148926.9","gene_symbol":"ADM","gene_name":"adrenomedullin [Source:HGNC Symbol;Acc:HGNC:259]","synonyms":"AM","biotype":"protein_coding","ncbi_id":"133","summary":"The protein encoded by this gene is a preprohormone which is cleaved to form two biologically active peptides, adrenomedullin and proadrenomedullin N-terminal 20 peptide. Adrenomedullin is a 52 aa peptide with several functions, including vasodilation, regulation of hormone secretion, promotion of angiogenesis, and antimicrobial activity. The antimicrobial activity is antibacterial, as the peptide has been shown to kill E. coli and S. aureus at low concentration. [provided by RefSeq, Aug 2014]","start":10304680,"end":10307397,"strand":1,"description":"adrenomedullin [Source:HGNC Symbol;Acc:HGNC:259]"}, {"versioned_ensembl_gene_id":"ENSG00000217181.1","gene_symbol":"AL139039.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10574749,"end":10575227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230819.1","gene_symbol":"ZNF736P5Y","gene_name":"zinc finger protein 736 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38597]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480711","summary":null,"start":25018499,"end":25019303,"strand":-1,"description":"zinc finger protein 736 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38597]"}, {"versioned_ensembl_gene_id":"ENSG00000278197.1","gene_symbol":"AC006338.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25009700,"end":25010769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271192.1","gene_symbol":"AC006058.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43996896,"end":43997443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229618.2","gene_symbol":"AC011287.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12726152,"end":13751920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177337.7","gene_symbol":"DLGAP1-AS1","gene_name":"DLGAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31676]","synonyms":"HsT914,FLJ35776","biotype":"antisense_RNA","ncbi_id":"649446","summary":null,"start":3593732,"end":3598352,"strand":1,"description":"DLGAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31676]"}, {"versioned_ensembl_gene_id":"ENSG00000273850.3","gene_symbol":"PPP2R3B","gene_name":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]","synonyms":"PR70,PR48,PPP2R3LY,PPP2R3L","biotype":"protein_coding","ncbi_id":"28227","summary":"Protein phosphatase 2 (formerly named type 2A) is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phosphatase 2 holoenzymes are heterotrimeric proteins composed of a structural subunit A, a catalytic subunit C, and a regulatory subunit B. The regulatory subunit is encoded by a diverse set of genes that have been grouped into the B/PR55, B'/PR61, and B''/PR72 families. These different regulatory subunits confer distinct enzymatic specificities and intracellular localizations to the holozenzyme. The product of this gene belongs to the B'' family. The B'' family has been further divided into subfamilies. The product of this gene belongs to the beta subfamily of regulatory subunit B''. [provided by RefSeq, Apr 2010]","start":333240,"end":385935,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]"}, {"versioned_ensembl_gene_id":"ENSG00000104671.7","gene_symbol":"DCTN6","gene_name":"dynactin subunit 6 [Source:HGNC Symbol;Acc:HGNC:16964]","synonyms":"WS-3","biotype":"protein_coding","ncbi_id":"10671","summary":"The protein encoded by this gene contains an RGD (Arg-Gly-Asp) motif in the N-terminal region, which confers adhesive properties to macromolecular proteins like fibronectin. It shares a high degree of sequence similarity with the mouse homolog, which has been suggested to play a role in mitochondrial biogenesis. The exact biological function of this gene is not known. [provided by RefSeq, Jul 2008]","start":30156297,"end":30183640,"strand":1,"description":"dynactin subunit 6 [Source:HGNC Symbol;Acc:HGNC:16964]"}, {"versioned_ensembl_gene_id":"ENSG00000176842.14","gene_symbol":"IRX5","gene_name":"iroquois homeobox 5 [Source:HGNC Symbol;Acc:HGNC:14361]","synonyms":"IRX-2a","biotype":"protein_coding","ncbi_id":"10265","summary":"This gene encodes a member of the iroquois homeobox gene family, which are involved in several embryonic developmental processes. Knockout mice lacking this gene show that it is required for retinal cone bipolar cell differentiation, and that it negatively regulates potassium channel gene expression in the heart to ensure coordinated cardiac repolarization. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":54930862,"end":54934485,"strand":1,"description":"iroquois homeobox 5 [Source:HGNC Symbol;Acc:HGNC:14361]"}, {"versioned_ensembl_gene_id":"ENSG00000260015.1","gene_symbol":"AC010547.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71539834,"end":71541825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153165.18","gene_symbol":"RGPD3","gene_name":"RANBP2-like and GRIP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:32416]","synonyms":"RGP3","biotype":"protein_coding","ncbi_id":"653489","summary":"This gene is located in a cluster of Ran-binding protein related genes on chromosome 2 which arose through duplication in primates. The encoded protein contains an N-terminal TPR (tetratricopeptide repeat) domain, two Ran-binding domains, and a C-terminal GRIP domain (golgin-97, RanBP2alpha, Imh1p and p230/golgin-245) domain. [provided by RefSeq, Sep 2011]","start":106391290,"end":106468376,"strand":-1,"description":"RANBP2-like and GRIP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:32416]"}, {"versioned_ensembl_gene_id":"ENSG00000260520.1","gene_symbol":"AC010547.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71513863,"end":71517849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236853.1","gene_symbol":"OR2R1P","gene_name":"olfactory receptor family 2 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8274]","synonyms":"OST058,OR2R1","biotype":"unitary_pseudogene","ncbi_id":"392132","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143488489,"end":143489402,"strand":-1,"description":"olfactory receptor family 2 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8274]"}, {"versioned_ensembl_gene_id":"ENSG00000229176.11","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"NG23,C6orf26","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31750175,"end":31752228,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000261376.1","gene_symbol":"AC022166.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80179129,"end":80180682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278843.4","gene_symbol":"MMP28","gene_name":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]","synonyms":"EPILYSIN,MMP-28,MMP-25,MM28","biotype":"protein_coding","ncbi_id":"79148","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction and tissue remodeling, and disease processes, such as asthma and metastasis. This gene encodes a secreted enzyme that degrades casein. Its expression pattern suggests that it plays a role in tissue homeostasis and in wound repair. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":35765873,"end":35795707,"strand":-1,"description":"matrix metallopeptidase 28 [Source:HGNC Symbol;Acc:HGNC:14366]"}, {"versioned_ensembl_gene_id":"ENSG00000228499.1","gene_symbol":"TMSB10P1","gene_name":"thymosin beta 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41949]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506723","summary":null,"start":235882362,"end":235882493,"strand":-1,"description":"thymosin beta 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41949]"}, {"versioned_ensembl_gene_id":"ENSG00000267013.5","gene_symbol":"LINC01929","gene_name":"long intergenic non-protein coding RNA 1929 [Source:HGNC Symbol;Acc:HGNC:52751]","synonyms":"CTD-2171N6.1","biotype":"lincRNA","ncbi_id":"101927229","summary":null,"start":55105904,"end":55124306,"strand":-1,"description":"long intergenic non-protein coding RNA 1929 [Source:HGNC Symbol;Acc:HGNC:52751]"}, {"versioned_ensembl_gene_id":"ENSG00000227533.5","gene_symbol":"SLC2A1-AS1","gene_name":"SLC2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44187]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440584","summary":null,"start":42959049,"end":42983358,"strand":1,"description":"SLC2A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44187]"}, {"versioned_ensembl_gene_id":"ENSG00000165891.15","gene_symbol":"E2F7","gene_name":"E2F transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:23820]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144455","summary":"E2F transcription factors, such as E2F7, play an essential role in the regulation of cell cycle progression (Di Stefano et al., 2003 [PubMed 14633988]).[supplied by OMIM, May 2008]","start":77021247,"end":77065580,"strand":-1,"description":"E2F transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:23820]"}, {"versioned_ensembl_gene_id":"ENSG00000249186.1","gene_symbol":"AC140125.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177857945,"end":177871194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236884.8","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32548950,"end":32583052,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000260772.1","gene_symbol":"AC012321.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":69703065,"end":69704652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229856.7","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21A,P450c21A,CYP21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":32084376,"end":32084894,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000257910.1","gene_symbol":"AC124784.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76878193,"end":76880352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235670.1","gene_symbol":"RPL21P40","gene_name":"ribosomal protein L21 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36189]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271158","summary":null,"start":32030196,"end":32030678,"strand":1,"description":"ribosomal protein L21 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36189]"}, {"versioned_ensembl_gene_id":"ENSG00000180801.13","gene_symbol":"ARSJ","gene_name":"arylsulfatase family member J [Source:HGNC Symbol;Acc:HGNC:26286]","synonyms":"FLJ23548","biotype":"protein_coding","ncbi_id":"79642","summary":"Sulfatases (EC 3.1.5.6), such as ARSJ, hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules (Sardiello et al., 2005 [PubMed 16174644]).[supplied by OMIM, Mar 2008]","start":113900284,"end":113979727,"strand":-1,"description":"arylsulfatase family member J [Source:HGNC Symbol;Acc:HGNC:26286]"}, {"versioned_ensembl_gene_id":"ENSG00000275748.4","gene_symbol":"ARL17B","gene_name":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]","synonyms":"ARL17","biotype":"protein_coding","ncbi_id":"100506084","summary":null,"start":45699087,"end":45820912,"strand":1,"description":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]"}, {"versioned_ensembl_gene_id":"ENSG00000232551.2","gene_symbol":"MTCO1P14","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075142","summary":null,"start":106804474,"end":106806032,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52016]"}, {"versioned_ensembl_gene_id":"ENSG00000233449.1","gene_symbol":"MTATP6P14","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52059]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075157","summary":null,"start":106802755,"end":106803427,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52059]"}, {"versioned_ensembl_gene_id":"ENSG00000235209.1","gene_symbol":"AL022318.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38921227,"end":38924708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283125.1","gene_symbol":"AC022726.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63207622,"end":63208168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280880.1","gene_symbol":"BX247885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42138063,"end":42139731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282463.1","gene_symbol":"AC216130.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103141340,"end":103141930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230219.3","gene_symbol":"FAM92A1P2","gene_name":"family with sequence similarity 92 member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32287]","synonyms":"MGC71735,MGC102964,FAM92A3","biotype":"transcribed_processed_pseudogene","ncbi_id":"403315","summary":null,"start":183037665,"end":183040119,"strand":1,"description":"family with sequence similarity 92 member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32287]"}, {"versioned_ensembl_gene_id":"ENSG00000281577.1","gene_symbol":"AC240720.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":198117723,"end":198119668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250130.1","gene_symbol":"AC090519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44354691,"end":44355692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270695.1","gene_symbol":"AL133393.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4529722,"end":4530008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278995.1","gene_symbol":"Z69720.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74683,"end":74961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270405.1","gene_symbol":"AC104692.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152366763,"end":152367015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235055.3","gene_symbol":"AL157407.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68043330,"end":68044233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102755.11","gene_symbol":"FLT1","gene_name":"fms related tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:3763]","synonyms":"VEGFR1,FLT","biotype":"protein_coding","ncbi_id":"2321","summary":"This gene encodes a member of the vascular endothelial growth factor receptor (VEGFR) family. VEGFR family members are receptor tyrosine kinases (RTKs) which contain an extracellular ligand-binding region with seven immunoglobulin (Ig)-like domains, a transmembrane segment, and a tyrosine kinase (TK) domain within the cytoplasmic domain. This protein binds to VEGFR-A, VEGFR-B and placental growth factor and plays an important role in angiogenesis and vasculogenesis. Expression of this receptor is found in vascular endothelial cells, placental trophoblast cells and peripheral blood monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Isoforms include a full-length transmembrane receptor isoform and shortened, soluble isoforms. The soluble isoforms are associated with the onset of pre-eclampsia.[provided by RefSeq, May 2009]","start":28300344,"end":28495145,"strand":-1,"description":"fms related tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:3763]"}, {"versioned_ensembl_gene_id":"ENSG00000233296.1","gene_symbol":"AC092159.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":677186,"end":697371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127914.16","gene_symbol":"AKAP9","gene_name":"A-kinase anchoring protein 9 [Source:HGNC Symbol;Acc:HGNC:379]","synonyms":"MU-RMS-40.16A,LQT11,KIAA0803,HYPERION,CG-NAP,AKAP450,YOTIAO,AKAP350,PRKA9,PPP1R45","biotype":"protein_coding","ncbi_id":"10142","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternate splicing of this gene results in at least two isoforms that localize to the centrosome and the Golgi apparatus, and interact with numerous signaling proteins from multiple signal transduction pathways. These signaling proteins include type II protein kinase A, serine/threonine kinase protein kinase N, protein phosphatase 1, protein phosphatase 2a, protein kinase C-epsilon and phosphodiesterase 4D3. [provided by RefSeq, Aug 2008]","start":91940867,"end":92110673,"strand":1,"description":"A-kinase anchoring protein 9 [Source:HGNC Symbol;Acc:HGNC:379]"}, {"versioned_ensembl_gene_id":"ENSG00000186930.4","gene_symbol":"KRTAP6-2","gene_name":"keratin associated protein 6-2 [Source:HGNC Symbol;Acc:HGNC:18932]","synonyms":"KAP6.2","biotype":"protein_coding","ncbi_id":"337967","summary":null,"start":30598590,"end":30598902,"strand":-1,"description":"keratin associated protein 6-2 [Source:HGNC Symbol;Acc:HGNC:18932]"}, {"versioned_ensembl_gene_id":"ENSG00000165046.12","gene_symbol":"LETM2","gene_name":"leucine zipper and EF-hand containing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:14648]","synonyms":"FLJ25409","biotype":"protein_coding","ncbi_id":"137994","summary":null,"start":38386207,"end":38409527,"strand":1,"description":"leucine zipper and EF-hand containing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:14648]"}, {"versioned_ensembl_gene_id":"ENSG00000188112.8","gene_symbol":"C6orf132","gene_name":"chromosome 6 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:21288]","synonyms":"bA7K24.2","biotype":"protein_coding","ncbi_id":"647024","summary":null,"start":42101118,"end":42142619,"strand":-1,"description":"chromosome 6 open reading frame 132 [Source:HGNC Symbol;Acc:HGNC:21288]"}, {"versioned_ensembl_gene_id":"ENSG00000157021.9","gene_symbol":"FAM92A1P1","gene_name":"family with sequence similarity 92 member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32278]","synonyms":"FAM92A2","biotype":"unprocessed_pseudogene","ncbi_id":"729073","summary":null,"start":41163162,"end":41164374,"strand":1,"description":"family with sequence similarity 92 member A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32278]"}, {"versioned_ensembl_gene_id":"ENSG00000203581.7","gene_symbol":"OR1F2P","gene_name":"olfactory receptor family 1 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8196]","synonyms":"OR1F3P,OR1F2,OLFMF2","biotype":"unprocessed_pseudogene","ncbi_id":"26184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3215611,"end":3216543,"strand":1,"description":"olfactory receptor family 1 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8196]"}, {"versioned_ensembl_gene_id":"ENSG00000165197.4","gene_symbol":"VEGFD","gene_name":"vascular endothelial growth factor D [Source:HGNC Symbol;Acc:HGNC:3708]","synonyms":"VEGF-D,FIGF","biotype":"protein_coding","ncbi_id":"2277","summary":"The protein encoded by this gene is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family and is active in angiogenesis, lymphangiogenesis, and endothelial cell growth. This secreted protein undergoes a complex proteolytic maturation, generating multiple processed forms which bind and activate VEGFR-2 and VEGFR-3 receptors. This protein is structurally and functionally similar to vascular endothelial growth factor C. Read-through transcription has been observed between this locus and the upstream PIR (GeneID 8544) locus. [provided by RefSeq, Feb 2011]","start":15345591,"end":15384376,"strand":-1,"description":"vascular endothelial growth factor D [Source:HGNC Symbol;Acc:HGNC:3708]"}, {"versioned_ensembl_gene_id":"ENSG00000178764.7","gene_symbol":"ZHX2","gene_name":"zinc fingers and homeoboxes 2 [Source:HGNC Symbol;Acc:HGNC:18513]","synonyms":"KIAA0854","biotype":"protein_coding","ncbi_id":"22882","summary":"The members of the zinc fingers and homeoboxes gene family are nuclear homodimeric transcriptional repressors that interact with the A subunit of nuclear factor-Y (NF-YA) and contain two C2H2-type zinc fingers and five homeobox DNA-binding domains. This gene encodes member 2 of this gene family. In addition to forming homodimers, this protein heterodimerizes with member 1 of the zinc fingers and homeoboxes family. [provided by RefSeq, Jul 2008]","start":122781394,"end":122974512,"strand":1,"description":"zinc fingers and homeoboxes 2 [Source:HGNC Symbol;Acc:HGNC:18513]"}, {"versioned_ensembl_gene_id":"ENSG00000188010.12","gene_symbol":"MORN2","gene_name":"MORN repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:30166]","synonyms":"MOPT","biotype":"protein_coding","ncbi_id":"729967","summary":null,"start":38875962,"end":38929072,"strand":1,"description":"MORN repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:30166]"}, {"versioned_ensembl_gene_id":"ENSG00000214319.2","gene_symbol":"CXADRP1","gene_name":"CXADR pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23770]","synonyms":"CXADRP,CAR","biotype":"processed_pseudogene","ncbi_id":"653108","summary":null,"start":13676022,"end":13677116,"strand":1,"description":"CXADR pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23770]"}, {"versioned_ensembl_gene_id":"ENSG00000281484.2","gene_symbol":"BTG3","gene_name":"BTG anti-proliferation factor 3 [Source:HGNC Symbol;Acc:HGNC:1132]","synonyms":"tob55,APRO4,ANA/BTG3,ANA","biotype":"protein_coding","ncbi_id":"10950","summary":"The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein might play a role in neurogenesis in the central nervous system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":17604145,"end":17612947,"strand":-1,"description":"BTG anti-proliferation factor 3 [Source:HGNC Symbol;Acc:HGNC:1132]"}, {"versioned_ensembl_gene_id":"ENSG00000278146.1","gene_symbol":"AC012409.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96230897,"end":96231145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277135.1","gene_symbol":"AC012409.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96139472,"end":96140452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126432.13","gene_symbol":"PRDX5","gene_name":"peroxiredoxin 5 [Source:HGNC Symbol;Acc:HGNC:9355]","synonyms":"SBBI10,PRXV,PRDX6,PMP20,PLP,MGC142285,MGC142283,MGC117264,B166,AOEB166,ACR1","biotype":"protein_coding","ncbi_id":"25824","summary":"This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein interacts with peroxisome receptor 1 and plays an antioxidant protective role in different tissues under normal conditions and during inflammatory processes. The use of alternate transcription start sites is thought to result in transcript variants that use different in-frame translational start codons to generate isoforms that are targeted to the mitochondrion (isoform L) or peroxisome/cytoplasm (isoform S). Multiple related pseudogenes have been defined for this gene. [provided by RefSeq, Nov 2017]","start":64318088,"end":64321811,"strand":1,"description":"peroxiredoxin 5 [Source:HGNC Symbol;Acc:HGNC:9355]"}, {"versioned_ensembl_gene_id":"ENSG00000282406.1","gene_symbol":"TRMT112P4","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288173","summary":null,"start":101356497,"end":101356875,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44023]"}, {"versioned_ensembl_gene_id":"ENSG00000216777.1","gene_symbol":"PRRC2CP1","gene_name":"proline rich coiled-coil 2C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23949]","synonyms":"BAT2L2P1,BAT2D1P1","biotype":"processed_pseudogene","ncbi_id":"360018","summary":null,"start":3549652,"end":3549810,"strand":-1,"description":"proline rich coiled-coil 2C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23949]"}, {"versioned_ensembl_gene_id":"ENSG00000260822.1","gene_symbol":"AC004656.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":24545516,"end":24550466,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120992.17","gene_symbol":"LYPLA1","gene_name":"lysophospholipase I [Source:HGNC Symbol;Acc:HGNC:6737]","synonyms":"LPL1","biotype":"protein_coding","ncbi_id":"10434","summary":"This gene encodes a member of the alpha/beta hydrolase superfamily. The encoded protein functions as a homodimer, exhibiting both depalmitoylating as well as lysophospholipase activity, and may be involved in Ras localization and signaling. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 4, 6, and 7. [provided by RefSeq, Jul 2013]","start":54046367,"end":54102017,"strand":-1,"description":"lysophospholipase I [Source:HGNC Symbol;Acc:HGNC:6737]"}, {"versioned_ensembl_gene_id":"ENSG00000271380.1","gene_symbol":"AL451085.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154961825,"end":154962623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166351.10","gene_symbol":"POTED","gene_name":"POTE ankyrin domain family member D [Source:HGNC Symbol;Acc:HGNC:23822]","synonyms":"POTE-21,POTE,CT104.1,ANKRD21,A26B3,POTE21","biotype":"protein_coding","ncbi_id":"317754","summary":null,"start":13609858,"end":13641585,"strand":1,"description":"POTE ankyrin domain family member D [Source:HGNC Symbol;Acc:HGNC:23822]"}, {"versioned_ensembl_gene_id":"ENSG00000231531.5","gene_symbol":"HINT1P1","gene_name":"histidine triad nucleotide binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18467]","synonyms":"HINTP1","biotype":"processed_pseudogene","ncbi_id":"730647","summary":null,"start":143312684,"end":143313061,"strand":-1,"description":"histidine triad nucleotide binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18467]"}, {"versioned_ensembl_gene_id":"ENSG00000261792.1","gene_symbol":"DNM1P28","gene_name":"dynamin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35175]","synonyms":"DNM1DN3-1,DNM1DN3@,DNM1DN3-3","biotype":"unprocessed_pseudogene","ncbi_id":"100132031","summary":null,"start":30098826,"end":30102093,"strand":-1,"description":"dynamin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35175]"}, {"versioned_ensembl_gene_id":"ENSG00000163348.3","gene_symbol":"PYGO2","gene_name":"pygopus family PHD finger 2 [Source:HGNC Symbol;Acc:HGNC:30257]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90780","summary":null,"start":154957026,"end":154963853,"strand":-1,"description":"pygopus family PHD finger 2 [Source:HGNC Symbol;Acc:HGNC:30257]"}, {"versioned_ensembl_gene_id":"ENSG00000235412.1","gene_symbol":"TTTY4B","gene_name":"testis-specific transcript, Y-linked 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31891]","synonyms":"LINC00124","biotype":"lincRNA","ncbi_id":"474149","summary":"There are three copies of this gene on chromosome Y. This record represents the middle copy, which is within the P1 palindrome. [provided by RefSeq, Jul 2008]","start":24570202,"end":24607025,"strand":1,"description":"testis-specific transcript, Y-linked 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31891]"}, {"versioned_ensembl_gene_id":"ENSG00000015592.16","gene_symbol":"STMN4","gene_name":"stathmin 4 [Source:HGNC Symbol;Acc:HGNC:16078]","synonyms":"RB3","biotype":"protein_coding","ncbi_id":"81551","summary":null,"start":27235323,"end":27258420,"strand":-1,"description":"stathmin 4 [Source:HGNC Symbol;Acc:HGNC:16078]"}, {"versioned_ensembl_gene_id":"ENSG00000157470.11","gene_symbol":"FAM81A","gene_name":"family with sequence similarity 81 member A [Source:HGNC Symbol;Acc:HGNC:28379]","synonyms":"MGC26690","biotype":"protein_coding","ncbi_id":"145773","summary":null,"start":59372693,"end":59523549,"strand":1,"description":"family with sequence similarity 81 member A [Source:HGNC Symbol;Acc:HGNC:28379]"}, {"versioned_ensembl_gene_id":"ENSG00000108839.11","gene_symbol":"ALOX12","gene_name":"arachidonate 12-lipoxygenase, 12S type [Source:HGNC Symbol;Acc:HGNC:429]","synonyms":"12S-LOX","biotype":"protein_coding","ncbi_id":"239","summary":"This gene encodes a member of the lipoxygenase family of proteins. The encoded enzyme acts on different polyunsaturated fatty acid substrates to generate bioactive lipid mediators including eicosanoids and lipoxins. The encoded enzyme and its reaction products have been shown to regulate platelet function. Elevated expression of this gene has been observed in pancreatic islets derived from human diabetes patients. Allelic variants in this gene may be associated with susceptibility to toxoplasmosis. Multiple pseudogenes of this gene have been identified in the human genome. [provided by RefSeq, Aug 2017]","start":6996065,"end":7010736,"strand":1,"description":"arachidonate 12-lipoxygenase, 12S type [Source:HGNC Symbol;Acc:HGNC:429]"}, {"versioned_ensembl_gene_id":"ENSG00000235047.1","gene_symbol":"AC016751.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":175897336,"end":175904232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229779.1","gene_symbol":"AC016751.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175904371,"end":175905502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262542.1","gene_symbol":"KRTAP29-1","gene_name":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]","synonyms":"KAP29.2","biotype":"protein_coding","ncbi_id":"100533177","summary":null,"start":41290456,"end":41291481,"strand":-1,"description":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]"}, {"versioned_ensembl_gene_id":"ENSG00000275759.1","gene_symbol":"AC026367.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118428281,"end":118428870,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100813.14","gene_symbol":"ACIN1","gene_name":"apoptotic chromatin condensation inducer 1 [Source:HGNC Symbol;Acc:HGNC:17066]","synonyms":"KIAA0670,fSAP152,ACINUS","biotype":"protein_coding","ncbi_id":"22985","summary":"Apoptosis is defined by several morphologic nuclear changes, including chromatin condensation and nuclear fragmentation. This gene encodes a nuclear protein that induces apoptotic chromatin condensation after activation by caspase-3, without inducing DNA fragmentation. This protein has also been shown to be a component of a splicing-dependent multiprotein exon junction complex (EJC) that is deposited at splice junctions on mRNAs, as a consequence of pre-mRNA splicing. It may thus be involved in mRNA metabolism associated with splicing. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":23058564,"end":23095614,"strand":-1,"description":"apoptotic chromatin condensation inducer 1 [Source:HGNC Symbol;Acc:HGNC:17066]"}, {"versioned_ensembl_gene_id":"ENSG00000232887.1","gene_symbol":"AC006466.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31119284,"end":31119572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163132.6","gene_symbol":"MSX1","gene_name":"msh homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7391]","synonyms":"OFC5,HYD1,HOX7","biotype":"protein_coding","ncbi_id":"4487","summary":"This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008]","start":4859666,"end":4863936,"strand":1,"description":"msh homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7391]"}, {"versioned_ensembl_gene_id":"ENSG00000253983.2","gene_symbol":"AC087627.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74199396,"end":74208441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253115.1","gene_symbol":"AC087672.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74103516,"end":74106744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227029.1","gene_symbol":"AL139237.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43912444,"end":43914236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251196.1","gene_symbol":"AC106760.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10652211,"end":10655925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257959.1","gene_symbol":"CR383656.11","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18555677,"end":18596310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275874.1","gene_symbol":"PICSAR","gene_name":"P38 inhibited cutaneous squamous cell carcinoma associated lincRNA [Source:HGNC Symbol;Acc:HGNC:19725]","synonyms":"PRED74,NLC1-C,NCRNA00162,LINC00162,C21orf113","biotype":"lincRNA","ncbi_id":"378825","summary":null,"start":44999208,"end":45004727,"strand":-1,"description":"P38 inhibited cutaneous squamous cell carcinoma associated lincRNA [Source:HGNC Symbol;Acc:HGNC:19725]"}, {"versioned_ensembl_gene_id":"ENSG00000204187.5","gene_symbol":"LINC00619","gene_name":"long intergenic non-protein coding RNA 619 [Source:HGNC Symbol;Acc:HGNC:31657]","synonyms":"C10orf136,bA168P8.1","biotype":"lincRNA","ncbi_id":"414260","summary":null,"start":43845306,"end":43850622,"strand":1,"description":"long intergenic non-protein coding RNA 619 [Source:HGNC Symbol;Acc:HGNC:31657]"}, {"versioned_ensembl_gene_id":"ENSG00000138792.9","gene_symbol":"ENPEP","gene_name":"glutamyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:3355]","synonyms":"gp160,CD249","biotype":"protein_coding","ncbi_id":"2028","summary":"The ENPEP gene encodes glutamyl aminopeptidase, a type II integral membrane protein with an extracellular zinc-binding domain. This protein can upregulate blood pressure by cleaving the N-terminal aspartate from angiotensin II, and can regulate blood vessel formation and enhance tumorigenesis in some tissues. Along with ANPEP and DPP4, ENPEP was found to be a candidate co-receptor for the coronavirus SARS-CoV-2, which causes COVID-19. [provided by RefSeq, Apr 2020]","start":110365733,"end":110565285,"strand":1,"description":"glutamyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:3355]"}, {"versioned_ensembl_gene_id":"ENSG00000166787.3","gene_symbol":"SAA3P","gene_name":"serum amyloid A3 pseudogene [Source:HGNC Symbol;Acc:HGNC:10515]","synonyms":"SAA3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"6290","summary":null,"start":18112472,"end":18116132,"strand":-1,"description":"serum amyloid A3 pseudogene [Source:HGNC Symbol;Acc:HGNC:10515]"}, {"versioned_ensembl_gene_id":"ENSG00000257595.2","gene_symbol":"LINC02356","gene_name":"long intergenic non-protein coding RNA 2356 [Source:HGNC Symbol;Acc:HGNC:53278]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369984","summary":null,"start":111369282,"end":111403310,"strand":1,"description":"long intergenic non-protein coding RNA 2356 [Source:HGNC Symbol;Acc:HGNC:53278]"}, {"versioned_ensembl_gene_id":"ENSG00000273006.1","gene_symbol":"AC009229.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38193348,"end":38193629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258433.1","gene_symbol":"AC087633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95034384,"end":95035737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280371.1","gene_symbol":"AL136967.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41405819,"end":41406561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133135.13","gene_symbol":"RNF128","gene_name":"ring finger protein 128, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:21153]","synonyms":"FLJ23516,GRAIL","biotype":"protein_coding","ncbi_id":"79589","summary":"The protein encoded by this gene is a type I transmembrane protein that localizes to the endocytic pathway. This protein contains a RING zinc-finger motif and has been shown to possess E3 ubiquitin ligase activity. Expression of this gene in retrovirally transduced T cell hybridoma significantly inhibits activation-induced IL2 and IL4 cytokine production. Induced expression of this gene was observed in anergic CD4(+) T cells, which suggested a role in the induction of anergic phenotype. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":106693794,"end":106796993,"strand":1,"description":"ring finger protein 128, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:21153]"}, {"versioned_ensembl_gene_id":"ENSG00000116161.17","gene_symbol":"CACYBP","gene_name":"calcyclin binding protein [Source:HGNC Symbol;Acc:HGNC:30423]","synonyms":"SIP,S100A6BP","biotype":"protein_coding","ncbi_id":"27101","summary":"The protein encoded by this gene is a calcyclin binding protein. It may be involved in calcium-dependent ubiquitination and subsequent proteosomal degradation of target proteins. It probably serves as a molecular bridge in ubiquitin E3 complexes and participates in the ubiquitin-mediated degradation of beta-catenin. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":174999163,"end":175011715,"strand":1,"description":"calcyclin binding protein [Source:HGNC Symbol;Acc:HGNC:30423]"}, {"versioned_ensembl_gene_id":"ENSG00000234549.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30619065,"end":30639047,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000228161.1","gene_symbol":"AC245452.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22046430,"end":22046591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276433.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724498,"end":54736060,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000229186.4","gene_symbol":"ADAM1A","gene_name":"ADAM metallopeptidase domain 1A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:187]","synonyms":"PH-30a,FTNAP,Ftna,ADAM1P,ADAM1","biotype":"unitary_pseudogene","ncbi_id":"8759","summary":null,"start":111899263,"end":111901391,"strand":1,"description":"ADAM metallopeptidase domain 1A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:187]"}, {"versioned_ensembl_gene_id":"ENSG00000277829.1","gene_symbol":"AL031651.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38233251,"end":38233799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228347.1","gene_symbol":"FTLP17","gene_name":"ferritin light chain pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642337","summary":null,"start":104153306,"end":104153830,"strand":-1,"description":"ferritin light chain pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37967]"}, {"versioned_ensembl_gene_id":"ENSG00000284491.1","gene_symbol":"AC020934.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12802072,"end":12804303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267212.1","gene_symbol":"AC018761.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12784539,"end":12785101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226769.1","gene_symbol":"GAPDHP54","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:38560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421319","summary":null,"start":46997596,"end":46998488,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:38560]"}, {"versioned_ensembl_gene_id":"ENSG00000243072.1","gene_symbol":"AF186996.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125679573,"end":125679781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130741.10","gene_symbol":"EIF2S3","gene_name":"eukaryotic translation initiation factor 2 subunit gamma [Source:HGNC Symbol;Acc:HGNC:3267]","synonyms":"EIF2gamma,EIF2G,EIF2","biotype":"protein_coding","ncbi_id":"1968","summary":"The protein encoded by this gene is the largest subunit of a heterotrimeric GTP-binding protein involved in the recruitment of methionyl-tRNA(i) to the 40 S ribosomal subunit. [provided by RefSeq, Jan 2010]","start":24054716,"end":24077971,"strand":1,"description":"eukaryotic translation initiation factor 2 subunit gamma [Source:HGNC Symbol;Acc:HGNC:3267]"}, {"versioned_ensembl_gene_id":"ENSG00000274039.1","gene_symbol":"AL355140.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69480662,"end":69482549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236861.6","gene_symbol":"AC006378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93969442,"end":94011113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123388.4","gene_symbol":"HOXC11","gene_name":"homeobox C11 [Source:HGNC Symbol;Acc:HGNC:5123]","synonyms":"HOX3H","biotype":"protein_coding","ncbi_id":"3227","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene binds to a promoter element of the lactase-phlorizin hydrolase. It also may play a role in early intestinal development. An alternatively spliced variant encoding a shorter isoform has been described but its full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":53973126,"end":53977643,"strand":1,"description":"homeobox C11 [Source:HGNC Symbol;Acc:HGNC:5123]"}, {"versioned_ensembl_gene_id":"ENSG00000249641.2","gene_symbol":"HOXC13-AS","gene_name":"HOXC13 antisense RNA [Source:HGNC Symbol;Acc:HGNC:43753]","synonyms":"HOXC-AS5","biotype":"antisense_RNA","ncbi_id":"100874366","summary":null,"start":53935328,"end":53939643,"strand":-1,"description":"HOXC13 antisense RNA [Source:HGNC Symbol;Acc:HGNC:43753]"}, {"versioned_ensembl_gene_id":"ENSG00000228162.1","gene_symbol":"AC097713.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234438328,"end":234462127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116883.8","gene_symbol":"AL591845.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36323734,"end":36329221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277650.1","gene_symbol":"AL133414.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54830903,"end":54845777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236028.1","gene_symbol":"AL354766.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46901143,"end":46901726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254251.1","gene_symbol":"AC103770.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90806474,"end":90859240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232079.6","gene_symbol":"LINC01697","gene_name":"long intergenic non-protein coding RNA 1697 [Source:HGNC Symbol;Acc:HGNC:52485]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"284825","summary":null,"start":28048404,"end":28137611,"strand":1,"description":"long intergenic non-protein coding RNA 1697 [Source:HGNC Symbol;Acc:HGNC:52485]"}, {"versioned_ensembl_gene_id":"ENSG00000260596.5","gene_symbol":"DUX4","gene_name":"double homeobox 4 [Source:HGNC Symbol;Acc:HGNC:50800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288687","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length; a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. The encoded protein has been reported to function as a transcriptional activator of paired-like homeodomain transcription factor 1 (PITX1; GeneID 5307). Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":190173774,"end":190185942,"strand":1,"description":"double homeobox 4 [Source:HGNC Symbol;Acc:HGNC:50800]"}, {"versioned_ensembl_gene_id":"ENSG00000234945.7","gene_symbol":"GTF3C2-AS1","gene_name":"GTF3C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40269]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505624","summary":null,"start":27335535,"end":27342599,"strand":1,"description":"GTF3C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40269]"}, {"versioned_ensembl_gene_id":"ENSG00000168454.11","gene_symbol":"TXNDC2","gene_name":"thioredoxin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16470]","synonyms":"SPTRX1","biotype":"protein_coding","ncbi_id":"84203","summary":null,"start":9885726,"end":9889275,"strand":1,"description":"thioredoxin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16470]"}, {"versioned_ensembl_gene_id":"ENSG00000135315.11","gene_symbol":"CEP162","gene_name":"centrosomal protein 162 [Source:HGNC Symbol;Acc:HGNC:21107]","synonyms":"QN1,KIAA1009,C6orf84","biotype":"protein_coding","ncbi_id":"22832","summary":null,"start":84124241,"end":84227635,"strand":-1,"description":"centrosomal protein 162 [Source:HGNC Symbol;Acc:HGNC:21107]"}, {"versioned_ensembl_gene_id":"ENSG00000234072.1","gene_symbol":"AC074117.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27356246,"end":27367622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214128.10","gene_symbol":"TMEM213","gene_name":"transmembrane protein 213 [Source:HGNC Symbol;Acc:HGNC:27220]","synonyms":null,"biotype":"protein_coding","ncbi_id":"155006","summary":null,"start":138797952,"end":138838101,"strand":1,"description":"transmembrane protein 213 [Source:HGNC Symbol;Acc:HGNC:27220]"}, {"versioned_ensembl_gene_id":"ENSG00000269256.1","gene_symbol":"AC024603.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76558350,"end":76560994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274923.1","gene_symbol":"AC005296.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7896514,"end":7896722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166788.9","gene_symbol":"SAAL1","gene_name":"serum amyloid A like 1 [Source:HGNC Symbol;Acc:HGNC:25158]","synonyms":"FLJ41463","biotype":"protein_coding","ncbi_id":"113174","summary":null,"start":18069935,"end":18106091,"strand":-1,"description":"serum amyloid A like 1 [Source:HGNC Symbol;Acc:HGNC:25158]"}, {"versioned_ensembl_gene_id":"ENSG00000253394.5","gene_symbol":"LINC00534","gene_name":"long intergenic non-protein coding RNA 534 [Source:HGNC Symbol;Acc:HGNC:43643]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874052","summary":null,"start":90221488,"end":90569318,"strand":1,"description":"long intergenic non-protein coding RNA 534 [Source:HGNC Symbol;Acc:HGNC:43643]"}, {"versioned_ensembl_gene_id":"ENSG00000236572.1","gene_symbol":"AC006369.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37744333,"end":37747046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163171.7","gene_symbol":"CDC42EP3","gene_name":"CDC42 effector protein 3 [Source:HGNC Symbol;Acc:HGNC:16943]","synonyms":"UB1,CEP3,BORG2","biotype":"protein_coding","ncbi_id":"10602","summary":"This gene encodes a member of a small family of guanosine triphosphate (GTP) metabolizing proteins that contain a CRIB (Cdc42, Rac interactive binding) domain. Members of this family of proteins act as effectors of CDC42 function. The encoded protein is involved in actin cytoskeleton re-organization during cell shape changes, including pseudopodia formation. A pseudogene of this gene is found on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":37641882,"end":37738468,"strand":-1,"description":"CDC42 effector protein 3 [Source:HGNC Symbol;Acc:HGNC:16943]"}, {"versioned_ensembl_gene_id":"ENSG00000236213.1","gene_symbol":"AC006369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37600136,"end":37646698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231784.8","gene_symbol":"DBIL5P","gene_name":"diazepam binding inhibitor-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38519]","synonyms":"ELP2P","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100131454","summary":null,"start":752660,"end":755336,"strand":1,"description":"diazepam binding inhibitor-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38519]"}, {"versioned_ensembl_gene_id":"ENSG00000253643.5","gene_symbol":"AC024958.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24490312,"end":24514829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052850.5","gene_symbol":"ALX4","gene_name":"ALX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:450]","synonyms":"PFM2,PFM,KIAA1788,FPP","biotype":"protein_coding","ncbi_id":"60529","summary":"This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2); an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS); a syndrome characterized by craniofacial anomalies, cognitive disability, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart. [provided by RefSeq, Oct 2009]","start":44260444,"end":44310166,"strand":-1,"description":"ALX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:450]"}, {"versioned_ensembl_gene_id":"ENSG00000237186.1","gene_symbol":"AC092418.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57530345,"end":57530967,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255451.1","gene_symbol":"AC010768.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44468464,"end":44470429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262616.1","gene_symbol":"KRTAP3-4P","gene_name":"keratin associated protein 3-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18919]","synonyms":"KRTAP3P1,KAP3A","biotype":"unprocessed_pseudogene","ncbi_id":"85345","summary":null,"start":41004608,"end":41004887,"strand":-1,"description":"keratin associated protein 3-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18919]"}, {"versioned_ensembl_gene_id":"ENSG00000253632.1","gene_symbol":"AC084026.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29527312,"end":29530323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114200.9","gene_symbol":"BCHE","gene_name":"butyrylcholinesterase [Source:HGNC Symbol;Acc:HGNC:983]","synonyms":"E1,CHE2,CHE1","biotype":"protein_coding","ncbi_id":"590","summary":"This gene encodes a cholinesterase enzyme and member of the type-B carboxylesterase/lipase family of proteins. The encoded enzyme exhibits broad substrate specificity and is involved in the detoxification of poisons including organophosphate nerve agents and pesticides, and the metabolism of drugs including cocaine, heroin and aspirin. Humans homozygous for certain mutations in this gene exhibit prolonged apnea after administration of the muscle relaxant succinylcholine. [provided by RefSeq, Jul 2016]","start":165772904,"end":165837472,"strand":-1,"description":"butyrylcholinesterase [Source:HGNC Symbol;Acc:HGNC:983]"}, {"versioned_ensembl_gene_id":"ENSG00000255106.1","gene_symbol":"AC010768.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44539778,"end":44540693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253182.1","gene_symbol":"AC084026.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29548171,"end":29564341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231346.5","gene_symbol":"LINC01160","gene_name":"long intergenic non-protein coding RNA 1160 [Source:HGNC Symbol;Acc:HGNC:49525]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129269","summary":null,"start":111599655,"end":111608723,"strand":-1,"description":"long intergenic non-protein coding RNA 1160 [Source:HGNC Symbol;Acc:HGNC:49525]"}, {"versioned_ensembl_gene_id":"ENSG00000198691.11","gene_symbol":"ABCA4","gene_name":"ATP binding cassette subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:34]","synonyms":"STGD1,STGD,RP19,FFM,CORD3,ARMD2,ABCR","biotype":"protein_coding","ncbi_id":"24","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This protein is a retina-specific ABC transporter with N-retinylidene-PE as a substrate. It is expressed exclusively in retina photoreceptor cells, and the gene product mediates transport of an essental molecule, all-trans-retinal aldehyde (atRAL), across the photoreceptor cell membrane. Mutations in this gene are found in patients diagnosed with Stargardt disease, a form of juvenile-onset macular degeneration. Mutations in this gene are also associated with retinitis pigmentosa-19, cone-rod dystrophy type 3, early-onset severe retinal dystrophy, fundus flavimaculatus, and macular degeneration age-related 2. [provided by RefSeq, Sep 2019]","start":93992835,"end":94121132,"strand":-1,"description":"ATP binding cassette subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:34]"}, {"versioned_ensembl_gene_id":"ENSG00000281720.1","gene_symbol":"DUX4L8","gene_name":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]","synonyms":"DUX2","biotype":"unprocessed_pseudogene","ncbi_id":"26583","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190067935,"end":190069209,"strand":1,"description":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]"}, {"versioned_ensembl_gene_id":"ENSG00000084734.8","gene_symbol":"GCKR","gene_name":"glucokinase regulator [Source:HGNC Symbol;Acc:HGNC:4196]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2646","summary":"This gene encodes a protein belonging to the GCKR subfamily of the SIS (Sugar ISomerase) family of proteins. The gene product is a regulatory protein that inhibits glucokinase in liver and pancreatic islet cells by binding non-covalently to form an inactive complex with the enzyme. This gene is considered a susceptibility gene candidate for a form of maturity-onset diabetes of the young (MODY). [provided by RefSeq, Jul 2008]","start":27496842,"end":27523684,"strand":1,"description":"glucokinase regulator [Source:HGNC Symbol;Acc:HGNC:4196]"}, {"versioned_ensembl_gene_id":"ENSG00000121933.18","gene_symbol":"TMIGD3","gene_name":"transmembrane and immunoglobulin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:51375]","synonyms":"AD026","biotype":"protein_coding","ncbi_id":"57413","summary":"This gene encodes a transmembrane and immunoglobulin domain-containing protein. Alternative splicing results in multiple transcript variants, one of which shares its 5' terminal exon with that of the overlapping adenosine A3 receptor gene (GeneID:140), thus resulting in a fusion product. [provided by RefSeq, Nov 2014]","start":111483348,"end":111563962,"strand":-1,"description":"transmembrane and immunoglobulin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:51375]"}, {"versioned_ensembl_gene_id":"ENSG00000276526.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54448346,"end":54452936,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000278657.1","gene_symbol":"AC245452.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22036344,"end":22040065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249333.1","gene_symbol":"AC245452.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22038643,"end":22039126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281652.1","gene_symbol":"DUX4L7","gene_name":"double homeobox 4 like 7 [Source:HGNC Symbol;Acc:HGNC:37266]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653543","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190071232,"end":190072506,"strand":1,"description":"double homeobox 4 like 7 [Source:HGNC Symbol;Acc:HGNC:37266]"}, {"versioned_ensembl_gene_id":"ENSG00000281058.1","gene_symbol":"DUX4L6","gene_name":"double homeobox 4 like 6 [Source:HGNC Symbol;Acc:HGNC:37265]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653544","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190074525,"end":190075799,"strand":1,"description":"double homeobox 4 like 6 [Source:HGNC Symbol;Acc:HGNC:37265]"}, {"versioned_ensembl_gene_id":"ENSG00000085117.11","gene_symbol":"CD82","gene_name":"CD82 molecule [Source:HGNC Symbol;Acc:HGNC:6210]","synonyms":"TSPAN27,ST6,R2,KAI1,IA4","biotype":"protein_coding","ncbi_id":"3732","summary":"This metastasis suppressor gene product is a membrane glycoprotein that is a member of the transmembrane 4 superfamily. Expression of this gene has been shown to be downregulated in tumor progression of human cancers and can be activated by p53 through a consensus binding sequence in the promoter. Its expression and that of p53 are strongly correlated, and the loss of expression of these two proteins is associated with poor survival for prostate cancer patients. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":44564427,"end":44620363,"strand":1,"description":"CD82 molecule [Source:HGNC Symbol;Acc:HGNC:6210]"}, {"versioned_ensembl_gene_id":"ENSG00000275462.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54459891,"end":54465035,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000233070.1","gene_symbol":"ZFY-AS1","gene_name":"ZFY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38798]","synonyms":"ZFYAS,ZFY-AS","biotype":"antisense_RNA","ncbi_id":"107987337","summary":null,"start":2966844,"end":3002626,"strand":-1,"description":"ZFY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38798]"}, {"versioned_ensembl_gene_id":"ENSG00000111667.13","gene_symbol":"USP5","gene_name":"ubiquitin specific peptidase 5 [Source:HGNC Symbol;Acc:HGNC:12628]","synonyms":"IsoT","biotype":"protein_coding","ncbi_id":"8078","summary":"Ubiquitin (see MIM 191339)-dependent proteolysis is a complex pathway of protein metabolism implicated in such diverse cellular functions as maintenance of chromatin structure, receptor function, and degradation of abnormal proteins. A late step of the process involves disassembly of the polyubiquitin chains on degraded proteins into ubiquitin monomers. USP5 disassembles branched polyubiquitin chains by a sequential exo mechanism, starting at the proximal end of the chain (Wilkinson et al., 1995 [PubMed 7578059]).[supplied by OMIM, Mar 2010]","start":6852128,"end":6866632,"strand":1,"description":"ubiquitin specific peptidase 5 [Source:HGNC Symbol;Acc:HGNC:12628]"}, {"versioned_ensembl_gene_id":"ENSG00000085831.15","gene_symbol":"TTC39A","gene_name":"tetratricopeptide repeat domain 39A [Source:HGNC Symbol;Acc:HGNC:18657]","synonyms":"KIAA0452,DEME-6,C1orf34","biotype":"protein_coding","ncbi_id":"22996","summary":null,"start":51287258,"end":51345116,"strand":-1,"description":"tetratricopeptide repeat domain 39A [Source:HGNC Symbol;Acc:HGNC:18657]"}, {"versioned_ensembl_gene_id":"ENSG00000280799.1","gene_symbol":"DUX4L5","gene_name":"double homeobox 4 like 5 [Source:HGNC Symbol;Acc:HGNC:38689]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653545","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190077818,"end":190079092,"strand":1,"description":"double homeobox 4 like 5 [Source:HGNC Symbol;Acc:HGNC:38689]"}, {"versioned_ensembl_gene_id":"ENSG00000140968.10","gene_symbol":"IRF8","gene_name":"interferon regulatory factor 8 [Source:HGNC Symbol;Acc:HGNC:5358]","synonyms":"ICSBP1,ICSBP,IRF-8","biotype":"protein_coding","ncbi_id":"3394","summary":"Interferon consensus sequence-binding protein (ICSBP) is a transcription factor of the interferon (IFN) regulatory factor (IRF) family. Proteins of this family are composed of a conserved DNA-binding domain in the N-terminal region and a divergent C-terminal region that serves as the regulatory domain. The IRF family proteins bind to the IFN-stimulated response element (ISRE) and regulate expression of genes stimulated by type I IFNs, namely IFN-alpha and IFN-beta. IRF family proteins also control expression of IFN-alpha and IFN-beta-regulated genes that are induced by viral infection. [provided by RefSeq, Jul 2008]","start":85898803,"end":85922609,"strand":1,"description":"interferon regulatory factor 8 [Source:HGNC Symbol;Acc:HGNC:5358]"}, {"versioned_ensembl_gene_id":"ENSG00000125037.12","gene_symbol":"EMC3","gene_name":"ER membrane protein complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:23999]","synonyms":"TMEM111","biotype":"protein_coding","ncbi_id":"55831","summary":null,"start":9962537,"end":10011116,"strand":-1,"description":"ER membrane protein complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:23999]"}, {"versioned_ensembl_gene_id":"ENSG00000115211.15","gene_symbol":"EIF2B4","gene_name":"eukaryotic translation initiation factor 2B subunit delta [Source:HGNC Symbol;Acc:HGNC:3260]","synonyms":"EIF2Bdelta,EIF2B,EIF-2B,DKFZP586J0119","biotype":"protein_coding","ncbi_id":"8890","summary":"Eukaryotic initiation factor 2B (EIF2B), which is necessary for protein synthesis, is a GTP exchange factor composed of five different subunits. The protein encoded by this gene is the fourth, or delta, subunit. Defects in this gene are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":27364352,"end":27370486,"strand":-1,"description":"eukaryotic translation initiation factor 2B subunit delta [Source:HGNC Symbol;Acc:HGNC:3260]"}, {"versioned_ensembl_gene_id":"ENSG00000258834.4","gene_symbol":"DUX4L4","gene_name":"double homeobox 4 like 4 [Source:HGNC Symbol;Acc:HGNC:38686]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441056","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190081118,"end":190082386,"strand":1,"description":"double homeobox 4 like 4 [Source:HGNC Symbol;Acc:HGNC:38686]"}, {"versioned_ensembl_gene_id":"ENSG00000230788.2","gene_symbol":"AL512661.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106070481,"end":106073202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280757.1","gene_symbol":"DUX4L1","gene_name":"double homeobox 4 like 1 [Source:HGNC Symbol;Acc:HGNC:3082]","synonyms":"DUX4","biotype":"unprocessed_pseudogene","ncbi_id":"22947","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190084412,"end":190085686,"strand":1,"description":"double homeobox 4 like 1 [Source:HGNC Symbol;Acc:HGNC:3082]"}, {"versioned_ensembl_gene_id":"ENSG00000134419.15","gene_symbol":"RPS15A","gene_name":"ribosomal protein S15a [Source:HGNC Symbol;Acc:HGNC:10389]","synonyms":"S15A","biotype":"protein_coding","ncbi_id":"6210","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S8P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":18781295,"end":18790383,"strand":-1,"description":"ribosomal protein S15a [Source:HGNC Symbol;Acc:HGNC:10389]"}, {"versioned_ensembl_gene_id":"ENSG00000157502.13","gene_symbol":"MUM1L1","gene_name":"MUM1 like 1 [Source:HGNC Symbol;Acc:HGNC:26583]","synonyms":"FLJ33516","biotype":"protein_coding","ncbi_id":"139221","summary":"This gene encodes a protein which contains a mutated melanoma-associated antigen 1 domain. Proteins which contain mutated antigens are expressed at high levels on certain types of cancers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]","start":106168305,"end":106208956,"strand":1,"description":"MUM1 like 1 [Source:HGNC Symbol;Acc:HGNC:26583]"}, {"versioned_ensembl_gene_id":"ENSG00000277526.4","gene_symbol":"AC245123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2589985,"end":2623382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184106.8","gene_symbol":"TREML3P","gene_name":"triggering receptor expressed on myeloid cells like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:30806]","synonyms":"TREML3,TLT3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"340206","summary":"TREML3 is located in a gene cluster on chromosome 6 with the single Ig variable (IgV) domain activating receptors TREM1 (MIM 605085) and TREM2 (MIM 605086), but it has distinct structural and functional properties (Allcock et al., 2003 [PubMed 12645956]).[supplied by OMIM, Mar 2008]","start":41208713,"end":41217947,"strand":-1,"description":"triggering receptor expressed on myeloid cells like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:30806]"}, {"versioned_ensembl_gene_id":"ENSG00000170425.3","gene_symbol":"ADORA2B","gene_name":"adenosine A2b receptor [Source:HGNC Symbol;Acc:HGNC:264]","synonyms":null,"biotype":"protein_coding","ncbi_id":"136","summary":"This gene encodes an adenosine receptor that is a member of the G protein-coupled receptor superfamily. This integral membrane protein stimulates adenylate cyclase activity in the presence of adenosine. This protein also interacts with netrin-1, which is involved in axon elongation. The gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":15944917,"end":15975746,"strand":1,"description":"adenosine A2b receptor [Source:HGNC Symbol;Acc:HGNC:264]"}, {"versioned_ensembl_gene_id":"ENSG00000264801.1","gene_symbol":"ERVFRD-3","gene_name":"endogenous retrovirus group FRD member 3 [Source:HGNC Symbol;Acc:HGNC:49792]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100533725","summary":null,"start":21929457,"end":21931073,"strand":1,"description":"endogenous retrovirus group FRD member 3 [Source:HGNC Symbol;Acc:HGNC:49792]"}, {"versioned_ensembl_gene_id":"ENSG00000265194.1","gene_symbol":"AL359922.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21858910,"end":21861926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134779.14","gene_symbol":"TPGS2","gene_name":"tubulin polyglutamylase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24561]","synonyms":"C18orf10,HsT3006,DKFZP586M1523","biotype":"protein_coding","ncbi_id":"25941","summary":"This gene encodes a protein that is a component of the neuronal polyglutamylase complex, which plays a role in post-translational addition of glutamate residues to C-terminal tubulin tails. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2012]","start":36777647,"end":36829216,"strand":-1,"description":"tubulin polyglutamylase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24561]"}, {"versioned_ensembl_gene_id":"ENSG00000116473.14","gene_symbol":"RAP1A","gene_name":"RAP1A, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9855]","synonyms":"SMGP21,KREV-1","biotype":"protein_coding","ncbi_id":"5906","summary":"This gene encodes a member of the Ras family of small GTPases. The encoded protein undergoes a change in conformational state and activity, depending on whether it is bound to GTP or GDP. This protein is activated by several types of guanine nucleotide exchange factors (GEFs), and inactivated by two groups of GTPase-activating proteins (GAPs). The activation status of the encoded protein is therefore affected by the balance of intracellular levels of GEFs and GAPs. The encoded protein regulates signaling pathways that affect cell proliferation and adhesion, and may play a role in tumor malignancy. Pseudogenes of this gene have been defined on chromosomes 14 and 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":111542218,"end":111716691,"strand":1,"description":"RAP1A, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9855]"}, {"versioned_ensembl_gene_id":"ENSG00000147883.10","gene_symbol":"CDKN2B","gene_name":"cyclin dependent kinase inhibitor 2B [Source:HGNC Symbol;Acc:HGNC:1788]","synonyms":"TP15,p15INK4b,P15,MTS2,INK4B,CDK4I","biotype":"protein_coding","ncbi_id":"1030","summary":"This gene lies adjacent to the tumor suppressor gene CDKN2A in a region that is frequently mutated and deleted in a wide variety of tumors. This gene encodes a cyclin-dependent kinase inhibitor, which forms a complex with CDK4 or CDK6, and prevents the activation of the CDK kinases, thus the encoded protein functions as a cell growth regulator that controls cell cycle G1 progression. The expression of this gene was found to be dramatically induced by TGF beta, which suggested its role in the TGF beta induced growth inhibition. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]","start":22002903,"end":22009363,"strand":-1,"description":"cyclin dependent kinase inhibitor 2B [Source:HGNC Symbol;Acc:HGNC:1788]"}, {"versioned_ensembl_gene_id":"ENSG00000120549.17","gene_symbol":"KIAA1217","gene_name":"KIAA1217 [Source:HGNC Symbol;Acc:HGNC:25428]","synonyms":"DKFZP761L0424,SKT,ETL4","biotype":"protein_coding","ncbi_id":"56243","summary":null,"start":23694746,"end":24547848,"strand":1,"description":"KIAA1217 [Source:HGNC Symbol;Acc:HGNC:25428]"}, {"versioned_ensembl_gene_id":"ENSG00000150201.14","gene_symbol":"FXYD4","gene_name":"FXYD domain containing ion transport regulator 4 [Source:HGNC Symbol;Acc:HGNC:4028]","synonyms":"CHIF","biotype":"protein_coding","ncbi_id":"53828","summary":"This gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD-domain containing ion transport regulator. FXYD4, originally named CHIF for channel-inducing factor, has been shown to modulate the properties of the Na,K-ATPase, as has FXYD2, also known as the gamma subunit of the Na,K-ATPase, and FXYD7. Transmembrane topology has been established for FXYD4 and two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. Alternatively spliced transcript variants encoding the same protein have been found.[provided by RefSeq, May 2010]","start":43371642,"end":43376335,"strand":1,"description":"FXYD domain containing ion transport regulator 4 [Source:HGNC Symbol;Acc:HGNC:4028]"}, {"versioned_ensembl_gene_id":"ENSG00000234954.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486834,"end":29487970,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000225967.9","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"ABCB3,PSF2,D6S217E,RING11","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32861254,"end":32878050,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000264717.5","gene_symbol":"NPY4R2","gene_name":"neuropeptide Y receptor Y42 [Source:HGNC Symbol;Acc:HGNC:52383]","synonyms":"CH17-360D5.1","biotype":"protein_coding","ncbi_id":"100996758","summary":null,"start":47918739,"end":47923524,"strand":1,"description":"neuropeptide Y receptor Y42 [Source:HGNC Symbol;Acc:HGNC:52383]"}, {"versioned_ensembl_gene_id":"ENSG00000282541.1","gene_symbol":"IGHJ3P","gene_name":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]","synonyms":"Jpsi3","biotype":"IG_J_pseudogene","ncbi_id":"28478","summary":null,"start":105864187,"end":105864236,"strand":-1,"description":"immunoglobulin heavy joining 3P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5537]"}, {"versioned_ensembl_gene_id":"ENSG00000232005.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"PBX2MHC,HOX12,G17","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32224129,"end":32229571,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000228526.6","gene_symbol":"MIR34AHG","gene_name":"MIR34A host gene [Source:HGNC Symbol;Acc:HGNC:51913]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106614088","summary":null,"start":9148011,"end":9196983,"strand":-1,"description":"MIR34A host gene [Source:HGNC Symbol;Acc:HGNC:51913]"}, {"versioned_ensembl_gene_id":"ENSG00000225735.1","gene_symbol":"NEK4P1","gene_name":"NIMA-related kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421718","summary":null,"start":17210469,"end":17211347,"strand":-1,"description":"NIMA-related kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39649]"}, {"versioned_ensembl_gene_id":"ENSG00000277758.4","gene_symbol":"FO681492.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":47750864,"end":47763592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243384.1","gene_symbol":"AC119424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58572744,"end":58574319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259910.1","gene_symbol":"AC120498.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1159548,"end":1160176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237735.2","gene_symbol":"AF130359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16754519,"end":16815688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260403.1","gene_symbol":"AC120498.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1156976,"end":1157974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225172.5","gene_symbol":"AC096631.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198983321,"end":198985400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177173.5","gene_symbol":"NAP1L4P1","gene_name":"nucleosome assembly protein 1 like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728589","summary":null,"start":116532936,"end":116534092,"strand":-1,"description":"nucleosome assembly protein 1 like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39740]"}, {"versioned_ensembl_gene_id":"ENSG00000271913.5","gene_symbol":"AL035530.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158988178,"end":159064925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130363.11","gene_symbol":"RSPH3","gene_name":"radial spoke head 3 homolog [Source:HGNC Symbol;Acc:HGNC:21054]","synonyms":"RSP3,RSHL2,dJ111C20.1","biotype":"protein_coding","ncbi_id":"83861","summary":"The protein encoded by this gene acts as a protein kinase A anchoring protein. Mutations in this gene cause primary ciliary dyskinesia; a disorder characterized by defects of the axoneme in motile cilia and sperm flagella. The homolog of this gene was first identified in the blue-green algae Chlamydomonas as encoding a radial spoke protein that formed a structural component of motile cilia and flagella. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]","start":158972871,"end":159000187,"strand":-1,"description":"radial spoke head 3 homolog [Source:HGNC Symbol;Acc:HGNC:21054]"}, {"versioned_ensembl_gene_id":"ENSG00000243612.5","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32852194,"end":32856479,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000224185.1","gene_symbol":"SNX18P9","gene_name":"sorting nexin 18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644576","summary":null,"start":64439346,"end":64440180,"strand":1,"description":"sorting nexin 18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39617]"}, {"versioned_ensembl_gene_id":"ENSG00000225801.1","gene_symbol":"RABEPKP1","gene_name":"Rab9 effector protein with kelch motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39791]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421226","summary":null,"start":71296210,"end":71297235,"strand":1,"description":"Rab9 effector protein with kelch motifs pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39791]"}, {"versioned_ensembl_gene_id":"ENSG00000174384.9","gene_symbol":"PMS2P6","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33514]","synonyms":"PMS2L14","biotype":"unprocessed_pseudogene","ncbi_id":"729453","summary":null,"start":73093657,"end":73105389,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33514]"}, {"versioned_ensembl_gene_id":"ENSG00000236753.5","gene_symbol":"MKLN1-AS","gene_name":"MKLN1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40374]","synonyms":"MKLN1-AS2","biotype":"processed_transcript","ncbi_id":"100506881","summary":null,"start":131309744,"end":131328222,"strand":-1,"description":"MKLN1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40374]"}, {"versioned_ensembl_gene_id":"ENSG00000233681.1","gene_symbol":"CEACAMP1","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1821]","synonyms":"CGM8","biotype":"unprocessed_pseudogene","ncbi_id":"1090","summary":null,"start":42620212,"end":42633034,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1821]"}, {"versioned_ensembl_gene_id":"ENSG00000226522.1","gene_symbol":"AC004994.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18892096,"end":18899433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244039.1","gene_symbol":"AC008040.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169931998,"end":169933229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219445.2","gene_symbol":"AC019155.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125229579,"end":125264291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177468.6","gene_symbol":"OLIG3","gene_name":"oligodendrocyte transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:18003]","synonyms":"bHLHe20,Bhlhb7","biotype":"protein_coding","ncbi_id":"167826","summary":null,"start":137492202,"end":137494250,"strand":-1,"description":"oligodendrocyte transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:18003]"}, {"versioned_ensembl_gene_id":"ENSG00000227687.1","gene_symbol":"AL713965.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":205935128,"end":205935768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271035.1","gene_symbol":"AC010385.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28897785,"end":28898274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267567.1","gene_symbol":"AC008736.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32718298,"end":32719595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170291.14","gene_symbol":"ELP5","gene_name":"elongator acetyltransferase complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:30617]","synonyms":"DERP6,C17orf81","biotype":"protein_coding","ncbi_id":"23587","summary":null,"start":7251416,"end":7259940,"strand":1,"description":"elongator acetyltransferase complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:30617]"}, {"versioned_ensembl_gene_id":"ENSG00000259676.1","gene_symbol":"AC103982.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88797413,"end":88798734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174502.18","gene_symbol":"SLC26A9","gene_name":"solute carrier family 26 member 9 [Source:HGNC Symbol;Acc:HGNC:14469]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115019","summary":"This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns. The product of this gene is a highly selective chloride ion channel regulated by WNK kinases. Alternative splicing results in multiple transcript variants encoding differing isoforms.[provided by RefSeq, Dec 2008]","start":205913048,"end":205943460,"strand":-1,"description":"solute carrier family 26 member 9 [Source:HGNC Symbol;Acc:HGNC:14469]"}, {"versioned_ensembl_gene_id":"ENSG00000224273.2","gene_symbol":"AC005077.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76108434,"end":76132187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273004.1","gene_symbol":"AL078644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":185317779,"end":185318530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251430.1","gene_symbol":"MTCO3P27","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52130]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075183","summary":null,"start":64606418,"end":64606613,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:52130]"}, {"versioned_ensembl_gene_id":"ENSG00000281076.2","gene_symbol":"ZDHHC8P1","gene_name":"zinc finger DHHC-type containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26461]","synonyms":"ZDHHC8P,FLJ31568","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"150244","summary":null,"start":23390606,"end":23402726,"strand":-1,"description":"zinc finger DHHC-type containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26461]"}, {"versioned_ensembl_gene_id":"ENSG00000174151.14","gene_symbol":"CYB561D1","gene_name":"cytochrome b561 family member D1 [Source:HGNC Symbol;Acc:HGNC:26804]","synonyms":"FLJ44753,FLJ39035","biotype":"protein_coding","ncbi_id":"284613","summary":null,"start":109494052,"end":109502932,"strand":1,"description":"cytochrome b561 family member D1 [Source:HGNC Symbol;Acc:HGNC:26804]"}, {"versioned_ensembl_gene_id":"ENSG00000149968.11","gene_symbol":"MMP3","gene_name":"matrix metallopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:7173]","synonyms":"STMY,STMY1","biotype":"protein_coding","ncbi_id":"4314","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. This gene encodes an enzyme which degrades fibronectin, laminin, collagens III, IV, IX, and X, and cartilage proteoglycans. The enzyme is thought to be involved in wound repair, progression of atherosclerosis, and tumor initiation. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3. [provided by RefSeq, Jul 2008]","start":102835801,"end":102843803,"strand":-1,"description":"matrix metallopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:7173]"}, {"versioned_ensembl_gene_id":"ENSG00000169914.5","gene_symbol":"OTUD3","gene_name":"OTU deubiquitinase 3 [Source:HGNC Symbol;Acc:HGNC:29038]","synonyms":"KIAA0459,DUBA4","biotype":"protein_coding","ncbi_id":"23252","summary":null,"start":19882513,"end":19912945,"strand":1,"description":"OTU deubiquitinase 3 [Source:HGNC Symbol;Acc:HGNC:29038]"}, {"versioned_ensembl_gene_id":"ENSG00000228892.9","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32175884,"end":32185768,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000152229.18","gene_symbol":"PSTPIP2","gene_name":"proline-serine-threonine phosphatase interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:9581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9050","summary":null,"start":45983536,"end":46072272,"strand":-1,"description":"proline-serine-threonine phosphatase interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:9581]"}, {"versioned_ensembl_gene_id":"ENSG00000237577.1","gene_symbol":"CR936921.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32758260,"end":32759090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132793.11","gene_symbol":"LPIN3","gene_name":"lipin 3 [Source:HGNC Symbol;Acc:HGNC:14451]","synonyms":"SMP2,LIPN3L","biotype":"protein_coding","ncbi_id":"64900","summary":"The protein encoded by this gene is a member of the lipin family of proteins, and all family members share strong homology in their C-terminal region. This protein is thought to form hetero-oligomers with other lipin family members, while one family member, lipin 1, can also form homo-oligomers. This protein contains conserved motifs for phosphatidate phosphatase 1 (PAP1) activity as well as a domain that interacts with a transcriptional co-activator. Lipin complexes act in the cytoplasm to catalyze the dephosphorylation of phosphatidic acid to produce diacylglycerol, which is the precursor of both triglycerides and phospholipids. Lipin complexes are also thought to regulate gene expression as transcriptional co-activators in the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":41340920,"end":41360582,"strand":1,"description":"lipin 3 [Source:HGNC Symbol;Acc:HGNC:14451]"}, {"versioned_ensembl_gene_id":"ENSG00000230463.2","gene_symbol":"HLA-DRB3","gene_name":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]","synonyms":"HLA-DR3B,HLA-DR3B","biotype":"protein_coding","ncbi_id":"3125","summary":"HLA-DRB3 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32558296,"end":32572041,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]"}, {"versioned_ensembl_gene_id":"ENSG00000258134.1","gene_symbol":"AC016954.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32227410,"end":32228154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276192.2","gene_symbol":"IGHE","gene_name":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3497","summary":null,"start":105600717,"end":105602504,"strand":-1,"description":"immunoglobulin heavy constant epsilon [Source:HGNC Symbol;Acc:HGNC:5522]"}, {"versioned_ensembl_gene_id":"ENSG00000232969.1","gene_symbol":"AP001062.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44339376,"end":44340470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213296.4","gene_symbol":"AC005521.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124480524,"end":124481395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271357.1","gene_symbol":"AC048344.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32100485,"end":32100735,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257852.1","gene_symbol":"AC048344.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32072734,"end":32072880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275860.1","gene_symbol":"AC005702.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60021072,"end":60022436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099942.12","gene_symbol":"CRKL","gene_name":"CRK like proto-oncogene, adaptor protein [Source:HGNC Symbol;Acc:HGNC:2363]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1399","summary":"This gene encodes a protein kinase containing SH2 and SH3 (src homology) domains which has been shown to activate the RAS and JUN kinase signaling pathways and transform fibroblasts in a RAS-dependent fashion. It is a substrate of the BCR-ABL tyrosine kinase, plays a role in fibroblast transformation by BCR-ABL, and may be oncogenic.[provided by RefSeq, Jan 2009]","start":20917426,"end":20953749,"strand":1,"description":"CRK like proto-oncogene, adaptor protein [Source:HGNC Symbol;Acc:HGNC:2363]"}, {"versioned_ensembl_gene_id":"ENSG00000256481.1","gene_symbol":"AP006333.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64081690,"end":64087175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127720.7","gene_symbol":"METTL25","gene_name":"methyltransferase like 25 [Source:HGNC Symbol;Acc:HGNC:26228]","synonyms":"FLJ22789,C12orf26","biotype":"protein_coding","ncbi_id":"84190","summary":null,"start":82358497,"end":82479236,"strand":1,"description":"methyltransferase like 25 [Source:HGNC Symbol;Acc:HGNC:26228]"}, {"versioned_ensembl_gene_id":"ENSG00000121390.18","gene_symbol":"PSPC1","gene_name":"paraspeckle component 1 [Source:HGNC Symbol;Acc:HGNC:20320]","synonyms":"FLJ10955,PSP1","biotype":"protein_coding","ncbi_id":"55269","summary":"This gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA-protein structures that include a non-coding RNA, NEAT1/Men epsilon/beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB/NONO and PSF/SFPQ proteins. Paraspeckles may function in the control of gene expression via an RNA nuclear retention mechanism. The protein encoded by this gene is found in paraspeckles in transcriptionally active cells, but it localizes to unique cap structures at the nucleolar periphery when RNA polymerase II transcription is inhibited, or during telophase. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene, which is also located on chromosome 13, has been identified. [provided by RefSeq, Aug 2011]","start":19674752,"end":19783019,"strand":-1,"description":"paraspeckle component 1 [Source:HGNC Symbol;Acc:HGNC:20320]"}, {"versioned_ensembl_gene_id":"ENSG00000158748.3","gene_symbol":"HTR6","gene_name":"5-hydroxytryptamine receptor 6 [Source:HGNC Symbol;Acc:HGNC:5301]","synonyms":"5-HT6R,5-HT6","biotype":"protein_coding","ncbi_id":"3362","summary":"This gene encodes a protein that belongs to the seven-transmembrane G protein-coupled receptor family of proteins. The encoded protein couples with the Gs alpha subunit and stimulates adenylate cyclase to activate the cyclic AMP-dependent signaling pathway. This receptor is thought to regulate cholinergic neuronal transmission in the brain. Several antidepressants and antipsychotic drugs have a high affinity for this receptor. [provided by RefSeq, Aug 2013]","start":19665287,"end":19679562,"strand":1,"description":"5-hydroxytryptamine receptor 6 [Source:HGNC Symbol;Acc:HGNC:5301]"}, {"versioned_ensembl_gene_id":"ENSG00000274765.1","gene_symbol":"AC018926.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55343141,"end":55343575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179295.17","gene_symbol":"PTPN11","gene_name":"protein tyrosine phosphatase, non-receptor type 11 [Source:HGNC Symbol;Acc:HGNC:9644]","synonyms":"SHP-2,SH-PTP2,PTP2C,NS1,BPTP3,SHP2","biotype":"protein_coding","ncbi_id":"5781","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. [provided by RefSeq, Aug 2016]","start":112418351,"end":112509913,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 11 [Source:HGNC Symbol;Acc:HGNC:9644]"}, {"versioned_ensembl_gene_id":"ENSG00000054148.17","gene_symbol":"PHPT1","gene_name":"phosphohistidine phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:30033]","synonyms":"PHP14,HSPC141,DKFZp564M173,CGI-202,bA216L13.10","biotype":"protein_coding","ncbi_id":"29085","summary":"This gene encodes an enzyme that catalyzes the reversible dephosphorylation of histidine residues in proteins. It may be involved in the dephosphorylation of G-beta and ATP citrate lyase and in negatively regulating CD4 T lymphocytes by dephosphorylation and inhibition of KCa3.1 channels. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":136848724,"end":136851027,"strand":1,"description":"phosphohistidine phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:30033]"}, {"versioned_ensembl_gene_id":"ENSG00000069943.9","gene_symbol":"PIGB","gene_name":"phosphatidylinositol glycan anchor biosynthesis class B [Source:HGNC Symbol;Acc:HGNC:8959]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9488","summary":"This gene encodes a transmembrane protein that is located in the endoplasmic reticulum and is involved in GPI-anchor biosynthesis. The glycosylphosphatidylinositol (GPI) anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This gene is thought to encode a member of a family of dolichol-phosphate-mannose (Dol-P-Man) dependent mannosyltransferases. [provided by RefSeq, Jul 2008]","start":55318960,"end":55355648,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class B [Source:HGNC Symbol;Acc:HGNC:8959]"}, {"versioned_ensembl_gene_id":"ENSG00000185633.10","gene_symbol":"NDUFA4L2","gene_name":"NDUFA4, mitochondrial complex associated like 2 [Source:HGNC Symbol;Acc:HGNC:29836]","synonyms":"NUOMS,FLJ26118","biotype":"protein_coding","ncbi_id":"56901","summary":null,"start":57234903,"end":57240715,"strand":-1,"description":"NDUFA4, mitochondrial complex associated like 2 [Source:HGNC Symbol;Acc:HGNC:29836]"}, {"versioned_ensembl_gene_id":"ENSG00000256061.7","gene_symbol":"DNAAF4","gene_name":"dynein axonemal assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:21493]","synonyms":"FLJ37882,EKN1,DYX1C1,CILD25","biotype":"protein_coding","ncbi_id":"161582","summary":"This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]","start":55410525,"end":55508234,"strand":-1,"description":"dynein axonemal assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:21493]"}, {"versioned_ensembl_gene_id":"ENSG00000010671.15","gene_symbol":"BTK","gene_name":"Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1133]","synonyms":"IMD1,ATK,AGMX1,XLA,PSCTK1","biotype":"protein_coding","ncbi_id":"695","summary":"The protein encoded by this gene plays a crucial role in B-cell development. Mutations in this gene cause X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes, and associated with a failure of Ig heavy chain rearrangement. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]","start":101349447,"end":101390796,"strand":-1,"description":"Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1133]"}, {"versioned_ensembl_gene_id":"ENSG00000232007.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"POLR2LP,AB023060.6","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31134461,"end":31134647,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000224408.1","gene_symbol":"USP9YP22","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:38758]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874383","summary":null,"start":9183694,"end":9185803,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:38758]"}, {"versioned_ensembl_gene_id":"ENSG00000229858.2","gene_symbol":"AC016831.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130822868,"end":130823219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228624.7","gene_symbol":"HDAC2-AS2","gene_name":"HDAC2 and HS3ST5 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43590]","synonyms":"ENST00000421891","biotype":"antisense_RNA","ncbi_id":"101927768","summary":null,"start":113969701,"end":114471705,"strand":1,"description":"HDAC2 and HS3ST5 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43590]"}, {"versioned_ensembl_gene_id":"ENSG00000255968.1","gene_symbol":"AC024145.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26318953,"end":26421462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087087.19","gene_symbol":"SRRT","gene_name":"serrate, RNA effector molecule [Source:HGNC Symbol;Acc:HGNC:24101]","synonyms":"serrate,Asr2,ARS2","biotype":"protein_coding","ncbi_id":"51593","summary":null,"start":100875111,"end":100888664,"strand":1,"description":"serrate, RNA effector molecule [Source:HGNC Symbol;Acc:HGNC:24101]"}, {"versioned_ensembl_gene_id":"ENSG00000282219.1","gene_symbol":"ELK2BP","gene_name":"ELK2B, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3324]","synonyms":"ELK2P2,ELK2.2","biotype":"unprocessed_pseudogene","ncbi_id":"9995","summary":null,"start":105546610,"end":105549694,"strand":-1,"description":"ELK2B, member of ETS oncogene family, pseudogene [Source:HGNC Symbol;Acc:HGNC:3324]"}, {"versioned_ensembl_gene_id":"ENSG00000224753.1","gene_symbol":"CR759956.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497578,"end":29510624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232974.3","gene_symbol":"CR759956.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489340,"end":29489745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267216.1","gene_symbol":"AC020915.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":58278966,"end":58315197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230989.6","gene_symbol":"HSBP1","gene_name":"heat shock factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3281","summary":"The heat-shock response is elicited by exposure of cells to thermal and chemical stress and through the activation of HSFs (heat shock factors) results in the elevated expression of heat-shock induced genes. Heat shock factor binding protein 1 (HSBP1), is a 76-amino-acid protein that binds to heat shock factor 1(HSF1), which is a transcription factor involved in the HS response. During HS response, HSF1 undergoes conformational transition from an inert non-DNA-binding monomer to active functional trimers. HSBP1 is nuclear-localized and interacts with the active trimeric state of HSF1 to negatively regulate HSF1 DNA-binding activity. Overexpression of HSBP1 in mammalian cells represses the transactivation activity of HSF1. When overexpressed in C.elegans HSBP1 has severe effects on survival of the animals after thermal and chemical stress consistent with a role of HSBP1 as a negative regulator of heat shock response. [provided by RefSeq, Jul 2008]","start":83807843,"end":83819737,"strand":1,"description":"heat shock factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5203]"}, {"versioned_ensembl_gene_id":"ENSG00000133065.10","gene_symbol":"SLC41A1","gene_name":"solute carrier family 41 member 1 [Source:HGNC Symbol;Acc:HGNC:19429]","synonyms":"MgtE","biotype":"protein_coding","ncbi_id":"254428","summary":null,"start":205789093,"end":205813748,"strand":-1,"description":"solute carrier family 41 member 1 [Source:HGNC Symbol;Acc:HGNC:19429]"}, {"versioned_ensembl_gene_id":"ENSG00000167791.12","gene_symbol":"CABP2","gene_name":"calcium binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1385]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51475","summary":"This gene belongs to a subfamily of calcium binding proteins that share similarity to calmodulin. Like calmodulin, these family members can likely stimulate calmodulin-dependent kinase II and the protein phosphatase calcineurin. Calcium binding proteins are an important component of calcium mediated cellular signal transduction. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":67518912,"end":67524517,"strand":-1,"description":"calcium binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1385]"}, {"versioned_ensembl_gene_id":"ENSG00000148832.15","gene_symbol":"PAOX","gene_name":"polyamine oxidase [Source:HGNC Symbol;Acc:HGNC:20837]","synonyms":"PAO","biotype":"protein_coding","ncbi_id":"196743","summary":null,"start":133379234,"end":133391694,"strand":1,"description":"polyamine oxidase [Source:HGNC Symbol;Acc:HGNC:20837]"}, {"versioned_ensembl_gene_id":"ENSG00000173212.4","gene_symbol":"MAB21L3","gene_name":"mab-21 like 3 [Source:HGNC Symbol;Acc:HGNC:26787]","synonyms":"FLJ38716,C1orf161","biotype":"protein_coding","ncbi_id":"126868","summary":null,"start":116111755,"end":116135240,"strand":1,"description":"mab-21 like 3 [Source:HGNC Symbol;Acc:HGNC:26787]"}, {"versioned_ensembl_gene_id":"ENSG00000226940.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29898524,"end":29899386,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000259959.1","gene_symbol":"AC107068.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47840122,"end":47844339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225872.3","gene_symbol":"LINC01529","gene_name":"long intergenic non-protein coding RNA 1529 [Source:HGNC Symbol;Acc:HGNC:51268]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644050","summary":null,"start":35785697,"end":35797902,"strand":-1,"description":"long intergenic non-protein coding RNA 1529 [Source:HGNC Symbol;Acc:HGNC:51268]"}, {"versioned_ensembl_gene_id":"ENSG00000265334.1","gene_symbol":"AC130324.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30834325,"end":30863028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236883.1","gene_symbol":"AP001615.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41739373,"end":41741308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184840.11","gene_symbol":"TMED9","gene_name":"transmembrane p24 trafficking protein 9 [Source:HGNC Symbol;Acc:HGNC:24878]","synonyms":"p24alpha2,p24a2,HSGP25L2G","biotype":"protein_coding","ncbi_id":"54732","summary":"This gene is a member of a family of genes encoding transport proteins located in the endoplasmic reticulum and the Golgi. A similar gene in mouse is the target of microRNA miR-296, which is part of an imprinted cluster. [provided by RefSeq, Jul 2016]","start":177592158,"end":177596124,"strand":1,"description":"transmembrane p24 trafficking protein 9 [Source:HGNC Symbol;Acc:HGNC:24878]"}, {"versioned_ensembl_gene_id":"ENSG00000174562.13","gene_symbol":"KLK15","gene_name":"kallikrein related peptidase 15 [Source:HGNC Symbol;Acc:HGNC:20453]","synonyms":"prostinogen,HSRNASPH,ACO","biotype":"protein_coding","ncbi_id":"55554","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. In prostate cancer, this gene has increased expression, which indicates its possible use as a diagnostic or prognostic marker for prostate cancer. The gene contains multiple polyadenylation sites and alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":50825289,"end":50837213,"strand":-1,"description":"kallikrein related peptidase 15 [Source:HGNC Symbol;Acc:HGNC:20453]"}, {"versioned_ensembl_gene_id":"ENSG00000130203.9","gene_symbol":"APOE","gene_name":"apolipoprotein E [Source:HGNC Symbol;Acc:HGNC:613]","synonyms":"AD2","biotype":"protein_coding","ncbi_id":"348","summary":"The protein encoded by this gene is a major apoprotein of the chylomicron. It binds to a specific liver and peripheral cell receptor, and is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. This gene maps to chromosome 19 in a cluster with the related apolipoprotein C1 and C2 genes. Mutations in this gene result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. [provided by RefSeq, Jun 2016]","start":44905754,"end":44909393,"strand":1,"description":"apolipoprotein E [Source:HGNC Symbol;Acc:HGNC:613]"}, {"versioned_ensembl_gene_id":"ENSG00000138161.13","gene_symbol":"CUZD1","gene_name":"CUB and zona pellucida like domains 1 [Source:HGNC Symbol;Acc:HGNC:17937]","synonyms":"UO-44,ERG-1","biotype":"protein_coding","ncbi_id":"50624","summary":null,"start":122832149,"end":122850793,"strand":-1,"description":"CUB and zona pellucida like domains 1 [Source:HGNC Symbol;Acc:HGNC:17937]"}, {"versioned_ensembl_gene_id":"ENSG00000256987.1","gene_symbol":"AC023050.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31953889,"end":31955268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242314.1","gene_symbol":"RPL12P32","gene_name":"ribosomal protein L12 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36597]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132795","summary":null,"start":31948334,"end":31948827,"strand":1,"description":"ribosomal protein L12 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36597]"}, {"versioned_ensembl_gene_id":"ENSG00000196313.11","gene_symbol":"POM121","gene_name":"POM121 transmembrane nucleoporin [Source:HGNC Symbol;Acc:HGNC:19702]","synonyms":"POM121A,KIAA0618,DKFZP586P2220,DKFZP586G1822","biotype":"protein_coding","ncbi_id":"9883","summary":"This gene encodes a transmembrane protein that localizes to the inner nuclear membrane and forms a core component of the nuclear pore complex, which mediates transport to and from the nucleus. The encoded protein may anchor this complex to the nuclear envelope. There are multiple related genes and pseudogenes for this gene on chromosomes 5, 7, 15, and 22. Alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2013]","start":72879365,"end":72951440,"strand":1,"description":"POM121 transmembrane nucleoporin [Source:HGNC Symbol;Acc:HGNC:19702]"}, {"versioned_ensembl_gene_id":"ENSG00000244436.2","gene_symbol":"AC023050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31897820,"end":31898123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236347.1","gene_symbol":"AL513123.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113531118,"end":113543793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153982.10","gene_symbol":"GDPD1","gene_name":"glycerophosphodiester phosphodiesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20883]","synonyms":"GDE4,FLJ37451","biotype":"protein_coding","ncbi_id":"284161","summary":"This gene encodes a member of the glycerophosphodiester phosphodiesterase family of enzymes that catalyze the hydrolysis of deacylated glycerophospholipids to glycerol phosphate and alcohol. The encoded protein is localized to the cytoplasm and concentrates near the perinuclear region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":59220467,"end":59275967,"strand":1,"description":"glycerophosphodiester phosphodiesterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20883]"}, {"versioned_ensembl_gene_id":"ENSG00000236526.1","gene_symbol":"AL035448.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11909404,"end":11918677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236118.1","gene_symbol":"AC245517.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22155582,"end":22155942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100341.11","gene_symbol":"PNPLA5","gene_name":"patatin like phospholipase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:24888]","synonyms":"GS2L,dJ388M5.4","biotype":"protein_coding","ncbi_id":"150379","summary":"This gene is a member of the patatin-like phospholipase family; its encoded protein has been shown to inhibit transacylation. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]","start":43879678,"end":43892013,"strand":-1,"description":"patatin like phospholipase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:24888]"}, {"versioned_ensembl_gene_id":"ENSG00000167107.12","gene_symbol":"ACSF2","gene_name":"acyl-CoA synthetase family member 2 [Source:HGNC Symbol;Acc:HGNC:26101]","synonyms":"FLJ20920,ACSMW","biotype":"protein_coding","ncbi_id":"80221","summary":null,"start":50426158,"end":50474845,"strand":1,"description":"acyl-CoA synthetase family member 2 [Source:HGNC Symbol;Acc:HGNC:26101]"}, {"versioned_ensembl_gene_id":"ENSG00000235399.1","gene_symbol":"AL135902.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136995170,"end":136999504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279310.1","gene_symbol":"AC073530.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67065018,"end":67065278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258981.1","gene_symbol":"COX5AP2","gene_name":"cytochrome c oxidase subunit 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319087","summary":null,"start":52117602,"end":52117995,"strand":1,"description":"cytochrome c oxidase subunit 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20005]"}, {"versioned_ensembl_gene_id":"ENSG00000249646.2","gene_symbol":"OR7E94P","gene_name":"olfactory receptor family 7 subfamily E member 94 pseudogene [Source:HGNC Symbol;Acc:HGNC:14789]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79273","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":79587302,"end":79588130,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 94 pseudogene [Source:HGNC Symbol;Acc:HGNC:14789]"}, {"versioned_ensembl_gene_id":"ENSG00000040731.10","gene_symbol":"CDH10","gene_name":"cadherin 10 [Source:HGNC Symbol;Acc:HGNC:1749]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1008","summary":"This gene encodes a type II classical cadherin of the cadherin superfamily. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature cadherin protein. These integral membrane proteins mediate calcium-dependent cell-cell adhesion and are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. The extracellular domain consists of 5 subdomains, each containing a cadherin motif, and appears to determine the specificity of the protein's homophilic cell adhesion activity. Type II (atypical) cadherins are defined based on their lack of a histidine-alanine-valine (HAV) cell adhesion recognition sequence specific to type I cadherins. This particular cadherin is predominantly expressed in brain and is putatively involved in synaptic adhesions, axon outgrowth and guidance. Mutations in this gene may be associated with lung squamous cell carcinoma and colorectal cancer in human patients. [provided by RefSeq, Nov 2015]","start":24487100,"end":24644978,"strand":-1,"description":"cadherin 10 [Source:HGNC Symbol;Acc:HGNC:1749]"}, {"versioned_ensembl_gene_id":"ENSG00000205330.4","gene_symbol":"OR6C1","gene_name":"olfactory receptor family 6 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8355]","synonyms":"OST267","biotype":"protein_coding","ncbi_id":"390321","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55314343,"end":55322364,"strand":1,"description":"olfactory receptor family 6 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8355]"}, {"versioned_ensembl_gene_id":"ENSG00000113263.12","gene_symbol":"ITK","gene_name":"IL2 inducible T-cell kinase [Source:HGNC Symbol;Acc:HGNC:6171]","synonyms":"EMT,PSCTK2,LYK","biotype":"protein_coding","ncbi_id":"3702","summary":"This gene encodes an intracellular tyrosine kinase expressed in T-cells. The protein contains both SH2 and SH3 domains which are often found in intracellular kinases. It is thought to play a role in T-cell proliferation and differentiation. [provided by RefSeq, Jul 2008]","start":157142933,"end":157255191,"strand":1,"description":"IL2 inducible T-cell kinase [Source:HGNC Symbol;Acc:HGNC:6171]"}, {"versioned_ensembl_gene_id":"ENSG00000170613.4","gene_symbol":"FAM71B","gene_name":"family with sequence similarity 71 member B [Source:HGNC Symbol;Acc:HGNC:28397]","synonyms":"MGC26988","biotype":"protein_coding","ncbi_id":"153745","summary":null,"start":157161846,"end":157166264,"strand":-1,"description":"family with sequence similarity 71 member B [Source:HGNC Symbol;Acc:HGNC:28397]"}, {"versioned_ensembl_gene_id":"ENSG00000253980.1","gene_symbol":"AC010609.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157199242,"end":157224380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281097.1","gene_symbol":"LINC01395","gene_name":"long intergenic non-protein coding RNA 1395 [Source:NCBI gene;Acc:101929557]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929557","summary":null,"start":129612116,"end":129617269,"strand":-1,"description":"long intergenic non-protein coding RNA 1395 [Source:NCBI gene;Acc:101929557]"}, {"versioned_ensembl_gene_id":"ENSG00000281386.1","gene_symbol":"AP003500.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129591493,"end":129612110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261341.6","gene_symbol":"AC010325.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50776141,"end":50793142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227431.5","gene_symbol":"CSE1L-AS1","gene_name":"CSE1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51232]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723483","summary":null,"start":49040463,"end":49046044,"strand":-1,"description":"CSE1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51232]"}, {"versioned_ensembl_gene_id":"ENSG00000225937.1","gene_symbol":"PCA3","gene_name":"prostate cancer associated 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:8637]","synonyms":"PCAT3,NCRNA00019,DD3","biotype":"antisense_RNA","ncbi_id":"50652","summary":"This gene produces a spliced, long non-coding RNA that is highly overexpressed in most types of prostate cancer cells and is used as a specific biomarker for this type of cancer. This gene is embedded in an intronic region of the prune2 gene on the opposite DNA strand. The transcript regulates prune2 levels through formation of a double-stranded RNA that undergoes adenosine deaminase acting on RNA-dependent adenosine-to-inosine RNA editing. In prostate cancer derived cells, overexpression of PCA induced downregulation of prune2, leading to decreased cell proliferation. Conversely, silencing in prostate cancer cells resulted in increased proliferation. Regulation of this gene appears to be sensitive to androgen-receptor activation, a molecular signature of prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2017]","start":76764436,"end":76787569,"strand":1,"description":"prostate cancer associated 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:8637]"}, {"versioned_ensembl_gene_id":"ENSG00000259678.1","gene_symbol":"AC066613.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51414097,"end":51498833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142511.4","gene_symbol":"GPR32","gene_name":"G protein-coupled receptor 32 [Source:HGNC Symbol;Acc:HGNC:4487]","synonyms":"RVDR1","biotype":"protein_coding","ncbi_id":"2854","summary":"This gene is intronless and encodes a member of the G-protein coupled receptor 1 family. The encoded protein binds to resolvin D1 and lipoxin A4 and has been linked to pulmonary inflammation. A related pseudogene has been identified on chromosome 19. [provided by RefSeq, Nov 2012]","start":50770464,"end":50771732,"strand":1,"description":"G protein-coupled receptor 32 [Source:HGNC Symbol;Acc:HGNC:4487]"}, {"versioned_ensembl_gene_id":"ENSG00000131591.17","gene_symbol":"C1orf159","gene_name":"chromosome 1 open reading frame 159 [Source:HGNC Symbol;Acc:HGNC:26062]","synonyms":"FLJ20584","biotype":"protein_coding","ncbi_id":"54991","summary":null,"start":1081818,"end":1116361,"strand":-1,"description":"chromosome 1 open reading frame 159 [Source:HGNC Symbol;Acc:HGNC:26062]"}, {"versioned_ensembl_gene_id":"ENSG00000164037.16","gene_symbol":"SLC9B1","gene_name":"solute carrier family 9 member B1 [Source:HGNC Symbol;Acc:HGNC:24244]","synonyms":"NHEDC1,NHA1","biotype":"protein_coding","ncbi_id":"150159","summary":"The protein encoded by this gene is a sodium/hydrogen exchanger and transmembrane protein. Highly conserved orthologs of this gene have been found in other mammalian species. The expression of this gene may be limited to testis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":102885048,"end":103019739,"strand":-1,"description":"solute carrier family 9 member B1 [Source:HGNC Symbol;Acc:HGNC:24244]"}, {"versioned_ensembl_gene_id":"ENSG00000249283.3","gene_symbol":"ACTR3BP4","gene_name":"ACTR3B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38681]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"777774","summary":null,"start":102961956,"end":102963327,"strand":1,"description":"ACTR3B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38681]"}, {"versioned_ensembl_gene_id":"ENSG00000187950.8","gene_symbol":"OVCH1","gene_name":"ovochymase 1 [Source:HGNC Symbol;Acc:HGNC:23080]","synonyms":"OVCH","biotype":"protein_coding","ncbi_id":"341350","summary":null,"start":29412474,"end":29497686,"strand":-1,"description":"ovochymase 1 [Source:HGNC Symbol;Acc:HGNC:23080]"}, {"versioned_ensembl_gene_id":"ENSG00000169499.14","gene_symbol":"PLEKHA2","gene_name":"pleckstrin homology domain containing A2 [Source:HGNC Symbol;Acc:HGNC:14336]","synonyms":"TAPP2","biotype":"protein_coding","ncbi_id":"59339","summary":null,"start":38901235,"end":38973909,"strand":1,"description":"pleckstrin homology domain containing A2 [Source:HGNC Symbol;Acc:HGNC:14336]"}, {"versioned_ensembl_gene_id":"ENSG00000124564.17","gene_symbol":"SLC17A3","gene_name":"solute carrier family 17 member 3 [Source:HGNC Symbol;Acc:HGNC:10931]","synonyms":"NPT4","biotype":"protein_coding","ncbi_id":"10786","summary":"The protein encoded by this gene is a voltage-driven transporter that excretes intracellular urate and organic anions from the blood into renal tubule cells. Two transcript variants encoding different isoforms have been found for this gene. The longer isoform is a plasma membrane protein with transporter activity while the shorter isoform localizes to the endoplasmic reticulum. [provided by RefSeq, Aug 2012]","start":25833066,"end":25882286,"strand":-1,"description":"solute carrier family 17 member 3 [Source:HGNC Symbol;Acc:HGNC:10931]"}, {"versioned_ensembl_gene_id":"ENSG00000182628.12","gene_symbol":"SKA2","gene_name":"spindle and kinetochore associated complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28006]","synonyms":"FLJ12758,FAM33A","biotype":"protein_coding","ncbi_id":"348235","summary":null,"start":59109951,"end":59155269,"strand":-1,"description":"spindle and kinetochore associated complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:28006]"}, {"versioned_ensembl_gene_id":"ENSG00000255053.1","gene_symbol":"OR4A44P","gene_name":"olfactory receptor family 4 subfamily A member 44 pseudogene [Source:HGNC Symbol;Acc:HGNC:31263]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403250","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48627546,"end":48628493,"strand":1,"description":"olfactory receptor family 4 subfamily A member 44 pseudogene [Source:HGNC Symbol;Acc:HGNC:31263]"}, {"versioned_ensembl_gene_id":"ENSG00000137473.17","gene_symbol":"TTC29","gene_name":"tetratricopeptide repeat domain 29 [Source:HGNC Symbol;Acc:HGNC:29936]","synonyms":"NYD-SP14","biotype":"protein_coding","ncbi_id":"83894","summary":null,"start":146706638,"end":146945882,"strand":-1,"description":"tetratricopeptide repeat domain 29 [Source:HGNC Symbol;Acc:HGNC:29936]"}, {"versioned_ensembl_gene_id":"ENSG00000238249.2","gene_symbol":"HMGN2P17","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39381]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100113373","summary":null,"start":8893409,"end":8894151,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39381]"}, {"versioned_ensembl_gene_id":"ENSG00000232208.2","gene_symbol":"AL139415.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8907393,"end":8907744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118579.12","gene_symbol":"MED28","gene_name":"mediator complex subunit 28 [Source:HGNC Symbol;Acc:HGNC:24628]","synonyms":"magicin,EG1,DKFZP434N185","biotype":"protein_coding","ncbi_id":"80306","summary":null,"start":17614631,"end":17634105,"strand":1,"description":"mediator complex subunit 28 [Source:HGNC Symbol;Acc:HGNC:24628]"}, {"versioned_ensembl_gene_id":"ENSG00000174500.12","gene_symbol":"GCSAM","gene_name":"germinal center associated signaling and motility [Source:HGNC Symbol;Acc:HGNC:20253]","synonyms":"HGAL,GCET2,MGC40441","biotype":"protein_coding","ncbi_id":"257144","summary":"This gene encodes a protein which may function in signal transduction pathways and whose expression is elevated in germinal cell lymphomas. It contains a putative PDZ-interacting domain, an immunoreceptor tyrosine-based activation motif (ITAM), and two putative SH2 binding sites. In B cells, its expression is specifically induced by interleukin-4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":112120841,"end":112133305,"strand":-1,"description":"germinal center associated signaling and motility [Source:HGNC Symbol;Acc:HGNC:20253]"}, {"versioned_ensembl_gene_id":"ENSG00000172058.15","gene_symbol":"SERF1A","gene_name":"small EDRK-rich factor 1A [Source:HGNC Symbol;Acc:HGNC:10755]","synonyms":"4F5,SMAM1,SERF1,H4F5,FAM2A","biotype":"protein_coding","ncbi_id":"8293","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The duplication region includes both a telomeric and a centromeric copy of this gene. Deletions of this gene, the telomeric copy, often accompany deletions of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients, and so it is thought that this gene may be a modifier of the SMA phenotype. The function of this protein is not known; however, it bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. [provided by RefSeq, Jul 2008]","start":70900665,"end":70918530,"strand":1,"description":"small EDRK-rich factor 1A [Source:HGNC Symbol;Acc:HGNC:10755]"}, {"versioned_ensembl_gene_id":"ENSG00000183530.13","gene_symbol":"PRR14L","gene_name":"proline rich 14 like [Source:HGNC Symbol;Acc:HGNC:28738]","synonyms":"MGC50372,C22orf30","biotype":"protein_coding","ncbi_id":"253143","summary":null,"start":31676256,"end":31750140,"strand":-1,"description":"proline rich 14 like [Source:HGNC Symbol;Acc:HGNC:28738]"}, {"versioned_ensembl_gene_id":"ENSG00000271671.1","gene_symbol":"AC107304.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96244732,"end":96245335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169604.19","gene_symbol":"ANTXR1","gene_name":"anthrax toxin receptor 1 [Source:HGNC Symbol;Acc:HGNC:21014]","synonyms":"TEM8,FLJ21776,FLJ10601,ATR","biotype":"protein_coding","ncbi_id":"84168","summary":"This gene encodes a type I transmembrane protein and is a tumor-specific endothelial marker that has been implicated in colorectal cancer. The encoded protein has been shown to also be a docking protein or receptor for Bacillus anthracis toxin, the causative agent of the disease, anthrax. The binding of the protective antigen (PA) component, of the tripartite anthrax toxin, to this receptor protein mediates delivery of toxin components to the cytosol of cells. Once inside the cell, the other two components of anthrax toxin, edema factor (EF) and lethal factor (LF) disrupt normal cellular processes. Three alternatively spliced variants that encode different protein isoforms have been described. [provided by RefSeq, Oct 2008]","start":69013178,"end":69249327,"strand":1,"description":"anthrax toxin receptor 1 [Source:HGNC Symbol;Acc:HGNC:21014]"}, {"versioned_ensembl_gene_id":"ENSG00000089048.14","gene_symbol":"ESF1","gene_name":"ESF1 nucleolar pre-rRNA processing protein homolog [Source:HGNC Symbol;Acc:HGNC:15898]","synonyms":"C20orf6,bA526K24.1","biotype":"protein_coding","ncbi_id":"51575","summary":null,"start":13714322,"end":13784886,"strand":-1,"description":"ESF1 nucleolar pre-rRNA processing protein homolog [Source:HGNC Symbol;Acc:HGNC:15898]"}, {"versioned_ensembl_gene_id":"ENSG00000113657.12","gene_symbol":"DPYSL3","gene_name":"dihydropyrimidinase like 3 [Source:HGNC Symbol;Acc:HGNC:3015]","synonyms":"ULIP,DRP-3,CRMP4","biotype":"protein_coding","ncbi_id":"1809","summary":null,"start":147390811,"end":147510056,"strand":-1,"description":"dihydropyrimidinase like 3 [Source:HGNC Symbol;Acc:HGNC:3015]"}, {"versioned_ensembl_gene_id":"ENSG00000280362.1","gene_symbol":"AC084759.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53910769,"end":53914712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089356.18","gene_symbol":"FXYD3","gene_name":"FXYD domain containing ion transport regulator 3 [Source:HGNC Symbol;Acc:HGNC:4027]","synonyms":"PLML,MAT-8","biotype":"protein_coding","ncbi_id":"5349","summary":"This gene belongs to a small family of FXYD-domain containing regulators of Na+/K+ ATPases which share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD, and containing 7 invariant and 6 highly conserved amino acids. This gene encodes a cell membrane protein that may regulate the function of ion-pumps and ion-channels. This gene may also play a role in tumor progression. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]","start":35115879,"end":35124324,"strand":1,"description":"FXYD domain containing ion transport regulator 3 [Source:HGNC Symbol;Acc:HGNC:4027]"}, {"versioned_ensembl_gene_id":"ENSG00000232415.1","gene_symbol":"AC005056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74059576,"end":74062284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235245.1","gene_symbol":"AL360181.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133295187,"end":133295977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213318.4","gene_symbol":"AC009078.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75192465,"end":75193247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231483.1","gene_symbol":"AL365356.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5608475,"end":5610793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234247.1","gene_symbol":"AC096537.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224661173,"end":224661886,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232296.1","gene_symbol":"AL691482.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202028606,"end":202028692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087303.17","gene_symbol":"NID2","gene_name":"nidogen 2 [Source:HGNC Symbol;Acc:HGNC:13389]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22795","summary":"This gene encodes a member of the nidogen family of basement membrane proteins. This protein is a cell-adhesion protein that binds collagens I and IV and laminin and may be involved in maintaining the structure of the basement membrane.[provided by RefSeq, Jun 2010]","start":52004803,"end":52069228,"strand":-1,"description":"nidogen 2 [Source:HGNC Symbol;Acc:HGNC:13389]"}, {"versioned_ensembl_gene_id":"ENSG00000234686.1","gene_symbol":"AC091730.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49230137,"end":49254816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226259.10","gene_symbol":"GTF2H2B","gene_name":"general transcription factor IIH subunit 2B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31393]","synonyms":"DKFZP686M0199","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653238","summary":null,"start":70415352,"end":70448015,"strand":1,"description":"general transcription factor IIH subunit 2B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31393]"}, {"versioned_ensembl_gene_id":"ENSG00000163728.10","gene_symbol":"TTC14","gene_name":"tetratricopeptide repeat domain 14 [Source:HGNC Symbol;Acc:HGNC:24697]","synonyms":"KIAA1980,FLJ00166","biotype":"protein_coding","ncbi_id":"151613","summary":null,"start":180602130,"end":180617828,"strand":1,"description":"tetratricopeptide repeat domain 14 [Source:HGNC Symbol;Acc:HGNC:24697]"}, {"versioned_ensembl_gene_id":"ENSG00000282254.1","gene_symbol":"AC004980.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76537175,"end":76615798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254757.1","gene_symbol":"AC127526.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3469319,"end":3531328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170955.9","gene_symbol":"CAVIN3","gene_name":"caveolae associated protein 3 [Source:HGNC Symbol;Acc:HGNC:9400]","synonyms":"MGC20400,HSRBC,cavin-3,SRBC,PRKCDBP","biotype":"protein_coding","ncbi_id":"112464","summary":"The protein encoded by this gene was identified as a binding protein of the protein kinase C, delta (PRKCD). The expression of this gene in cultured cell lines is strongly induced by serum starvation. The expression of this protein was found to be down-regulated in various cancer cell lines, suggesting the possible tumor suppressor function of this protein. [provided by RefSeq, Jul 2008]","start":6318946,"end":6320647,"strand":-1,"description":"caveolae associated protein 3 [Source:HGNC Symbol;Acc:HGNC:9400]"}, {"versioned_ensembl_gene_id":"ENSG00000257551.1","gene_symbol":"HLX-AS1","gene_name":"HLX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42509]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873924","summary":null,"start":220832763,"end":220880140,"strand":-1,"description":"HLX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42509]"}, {"versioned_ensembl_gene_id":"ENSG00000225103.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32670013,"end":32675872,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000238078.1","gene_symbol":"LINC01352","gene_name":"long intergenic non-protein coding RNA 1352 [Source:HGNC Symbol;Acc:HGNC:50578]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929730","summary":null,"start":220829255,"end":220832429,"strand":1,"description":"long intergenic non-protein coding RNA 1352 [Source:HGNC Symbol;Acc:HGNC:50578]"}, {"versioned_ensembl_gene_id":"ENSG00000279914.1","gene_symbol":"AL008638.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27040197,"end":27041494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111647.12","gene_symbol":"UHRF1BP1L","gene_name":"UHRF1 binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:29102]","synonyms":"KIAA0701","biotype":"protein_coding","ncbi_id":"23074","summary":null,"start":100028455,"end":100142848,"strand":-1,"description":"UHRF1 binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:29102]"}, {"versioned_ensembl_gene_id":"ENSG00000198673.10","gene_symbol":"FAM19A2","gene_name":"family with sequence similarity 19 member A2, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21589]","synonyms":"TAFA2,TAFA-2","biotype":"protein_coding","ncbi_id":"338811","summary":"This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines, that act as regulators of immune and nervous cells. [provided by RefSeq, Jul 2008]","start":61708259,"end":62279150,"strand":-1,"description":"family with sequence similarity 19 member A2, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21589]"}, {"versioned_ensembl_gene_id":"ENSG00000280707.2","gene_symbol":"AL353747.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167228300,"end":167237511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280211.1","gene_symbol":"AC106886.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30773532,"end":30776033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205571.13","gene_symbol":"SMN2","gene_name":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]","synonyms":"BCD541,TDRD16B,SMNC,GEMIN1","biotype":"protein_coding","ncbi_id":"6607","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Sep 2008]","start":70049612,"end":70078522,"strand":1,"description":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]"}, {"versioned_ensembl_gene_id":"ENSG00000280344.1","gene_symbol":"AC009166.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51176066,"end":51178898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165084.15","gene_symbol":"C8orf34","gene_name":"chromosome 8 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:30905]","synonyms":"VEST1,vest-1","biotype":"protein_coding","ncbi_id":"116328","summary":"This gene encodes a protein that is related to the cyclic AMP dependent protein kinase regulators. Naturally occurring mutations in this gene are associated with an increased risk for severe toxicities, such as diarrhea and neutropenia, in patients undergoing chemotherapeutic treatment. [provided by RefSeq, Mar 2017]","start":68330722,"end":68819022,"strand":1,"description":"chromosome 8 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:30905]"}, {"versioned_ensembl_gene_id":"ENSG00000223463.3","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29878611,"end":29881327,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000069248.11","gene_symbol":"NUP133","gene_name":"nucleoporin 133 [Source:HGNC Symbol;Acc:HGNC:18016]","synonyms":"FLJ10814","biotype":"protein_coding","ncbi_id":"55746","summary":"The nuclear envelope creates distinct nuclear and cytoplasmic compartments in eukaryotic cells. It consists of two concentric membranes perforated by nuclear pores, large protein complexes that form aqueous channels to regulate the flow of macromolecules between the nucleus and the cytoplasm. These complexes are composed of at least 100 different polypeptide subunits, many of which belong to the nucleoporin family. The nucleoporin protein encoded by this gene displays evolutionarily conserved interactions with other nucleoporins. This protein, which localizes to both sides of the nuclear pore complex at interphase, remains associated with the complex during mitosis and is targeted at early stages to the reforming nuclear envelope. This protein also localizes to kinetochores of mitotic cells. [provided by RefSeq, Jul 2008]","start":229440260,"end":229508341,"strand":-1,"description":"nucleoporin 133 [Source:HGNC Symbol;Acc:HGNC:18016]"}, {"versioned_ensembl_gene_id":"ENSG00000235876.2","gene_symbol":"FEM1AP4","gene_name":"fem-1 homolog A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39832]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729524","summary":null,"start":18665235,"end":18667221,"strand":1,"description":"fem-1 homolog A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39832]"}, {"versioned_ensembl_gene_id":"ENSG00000258837.1","gene_symbol":"AL133370.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68125004,"end":68130196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283776.1","gene_symbol":"AC233724.17","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17632088,"end":17632684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249337.2","gene_symbol":"SNX18P25","gene_name":"sorting nexin 18 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39633]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419005","summary":null,"start":49588772,"end":49589529,"strand":1,"description":"sorting nexin 18 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39633]"}, {"versioned_ensembl_gene_id":"ENSG00000269026.2","gene_symbol":"AC003006.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57682045,"end":57753575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282034.1","gene_symbol":"AC106886.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30704067,"end":30745169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264064.2","gene_symbol":"AC226154.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11880784,"end":11881057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204577.11","gene_symbol":"LILRB3","gene_name":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]","synonyms":"LIR-3,ILT5,PIRB,HL9,PIR-B,CD85a,LIR3","biotype":"protein_coding","ncbi_id":"11025","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54216278,"end":54223506,"strand":-1,"description":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]"}, {"versioned_ensembl_gene_id":"ENSG00000159307.18","gene_symbol":"SCUBE1","gene_name":"signal peptide, CUB domain and EGF like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80274","summary":"This gene encodes a cell surface glycoprotein that is a member of the SCUBE (signal peptide, CUB domain, EGF (epidermal growth factor)-like protein) family. Family members have an amino-terminal signal peptide, nine copies of EGF-like repeats and a CUB domain at the carboxyl terminus. This protein is expressed in platelets and endothelial cells and may play an important role in vascular biology. [provided by RefSeq, Oct 2011]","start":43197283,"end":43343388,"strand":-1,"description":"signal peptide, CUB domain and EGF like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13441]"}, {"versioned_ensembl_gene_id":"ENSG00000213762.11","gene_symbol":"ZNF134","gene_name":"zinc finger protein 134 [Source:HGNC Symbol;Acc:HGNC:12918]","synonyms":"pHZ-15","biotype":"protein_coding","ncbi_id":"7693","summary":null,"start":57614233,"end":57624723,"strand":1,"description":"zinc finger protein 134 [Source:HGNC Symbol;Acc:HGNC:12918]"}, {"versioned_ensembl_gene_id":"ENSG00000229502.5","gene_symbol":"AL391863.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157872571,"end":157875210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269097.1","gene_symbol":"TPRG1LP1","gene_name":"tumor protein p63 regulated 1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52353]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130490","summary":null,"start":57664280,"end":57665039,"strand":1,"description":"tumor protein p63 regulated 1 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52353]"}, {"versioned_ensembl_gene_id":"ENSG00000220867.1","gene_symbol":"HSPE1P26","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:49345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481677","summary":null,"start":157924402,"end":157924676,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:49345]"}, {"versioned_ensembl_gene_id":"ENSG00000142530.10","gene_symbol":"FAM71E1","gene_name":"family with sequence similarity 71 member E1 [Source:HGNC Symbol;Acc:HGNC:25107]","synonyms":null,"biotype":"protein_coding","ncbi_id":"112703","summary":null,"start":50466785,"end":50476753,"strand":-1,"description":"family with sequence similarity 71 member E1 [Source:HGNC Symbol;Acc:HGNC:25107]"}, {"versioned_ensembl_gene_id":"ENSG00000115523.16","gene_symbol":"GNLY","gene_name":"granulysin [Source:HGNC Symbol;Acc:HGNC:4414]","synonyms":"TLA519,NKG5,LAG2,LAG-2,D2S69E","biotype":"protein_coding","ncbi_id":"10578","summary":"The product of this gene is a member of the saposin-like protein (SAPLIP) family and is located in the cytotoxic granules of T cells, which are released upon antigen stimulation. This protein is present in cytotoxic granules of cytotoxic T lymphocytes and natural killer cells, and it has antimicrobial activity against M. tuberculosis and other organisms. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":85685175,"end":85698854,"strand":1,"description":"granulysin [Source:HGNC Symbol;Acc:HGNC:4414]"}, {"versioned_ensembl_gene_id":"ENSG00000224186.8","gene_symbol":"C5orf66","gene_name":"chromosome 5 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:48332]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996485","summary":null,"start":135033280,"end":135358219,"strand":1,"description":"chromosome 5 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:48332]"}, {"versioned_ensembl_gene_id":"ENSG00000170889.13","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54200742,"end":54249003,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000240929.2","gene_symbol":"HIST2H2BB","gene_name":"histone cluster 2 H2B family member b (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20654]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"338391","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 1. [provided by RefSeq, Oct 2015]","start":143875171,"end":143904650,"strand":-1,"description":"histone cluster 2 H2B family member b (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20654]"}, {"versioned_ensembl_gene_id":"ENSG00000217408.2","gene_symbol":"PRELID1P2","gene_name":"PRELI domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43887]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419971","summary":null,"start":25678769,"end":25679164,"strand":-1,"description":"PRELI domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43887]"}, {"versioned_ensembl_gene_id":"ENSG00000257198.6","gene_symbol":"FAM205BP","gene_name":"family with sequence similarity 205 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:24504]","synonyms":"FAM205B,DKFZp434J193,C9orf144A,C9orf144","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"389715","summary":null,"start":34832295,"end":34838586,"strand":-1,"description":"family with sequence similarity 205 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:24504]"}, {"versioned_ensembl_gene_id":"ENSG00000187097.12","gene_symbol":"ENTPD5","gene_name":"ectonucleoside triphosphate diphosphohydrolase 5 [Source:HGNC Symbol;Acc:HGNC:3367]","synonyms":"PCPH,NTPDase-5,CD39L4","biotype":"protein_coding","ncbi_id":"957","summary":"The protein encoded by this gene is similar to E-type nucleotidases (NTPases)/ecto-ATPase/apyrases. NTPases, such as CD39, mediate catabolism of extracellular nucleotides. ENTPD5 contains 4 apyrase-conserved regions which is characteristic of NTPases. [provided by RefSeq, Jan 2009]","start":73958010,"end":74019399,"strand":-1,"description":"ectonucleoside triphosphate diphosphohydrolase 5 [Source:HGNC Symbol;Acc:HGNC:3367]"}, {"versioned_ensembl_gene_id":"ENSG00000174930.4","gene_symbol":"VN2R1P","gene_name":"vomeronasal 2 receptor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:30344]","synonyms":"GPRC2B,CASRL1","biotype":"unitary_pseudogene","ncbi_id":"344760","summary":null,"start":156019646,"end":156037647,"strand":1,"description":"vomeronasal 2 receptor 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:30344]"}, {"versioned_ensembl_gene_id":"ENSG00000249790.2","gene_symbol":"AC092490.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8788257,"end":8795789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154040.20","gene_symbol":"CABYR","gene_name":"calcium binding tyrosine phosphorylation regulated [Source:HGNC Symbol;Acc:HGNC:15569]","synonyms":"FSP-2,CT88,CBP86","biotype":"protein_coding","ncbi_id":"26256","summary":"To reach fertilization competence, spermatozoa undergo a series of morphological and molecular maturational processes, termed capacitation, involving protein tyrosine phosphorylation and increased intracellular calcium. The protein encoded by this gene localizes to the principal piece of the sperm flagellum in association with the fibrous sheath and exhibits calcium-binding when phosphorylated during capacitation. A pseudogene on chromosome 3 has been identified for this gene. Alternatively spliced transcript variants encoding distinct protein isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":24138956,"end":24161603,"strand":1,"description":"calcium binding tyrosine phosphorylation regulated [Source:HGNC Symbol;Acc:HGNC:15569]"}, {"versioned_ensembl_gene_id":"ENSG00000075399.13","gene_symbol":"VPS9D1","gene_name":"VPS9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13526]","synonyms":"ATP-BL,C16orf7","biotype":"protein_coding","ncbi_id":"9605","summary":null,"start":89707134,"end":89720986,"strand":-1,"description":"VPS9 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13526]"}, {"versioned_ensembl_gene_id":"ENSG00000234060.1","gene_symbol":"EDDM3CP","gene_name":"epididymal protein 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:19224]","synonyms":"HE3-GAMMA,FAM12CP","biotype":"processed_pseudogene","ncbi_id":"266643","summary":null,"start":134319654,"end":134320078,"strand":-1,"description":"epididymal protein 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:19224]"}, {"versioned_ensembl_gene_id":"ENSG00000269967.1","gene_symbol":"AL136115.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31851913,"end":31921841,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100393.12","gene_symbol":"EP300","gene_name":"E1A binding protein p300 [Source:HGNC Symbol;Acc:HGNC:3373]","synonyms":"p300,KAT3B","biotype":"protein_coding","ncbi_id":"2033","summary":"This gene encodes the adenovirus E1A-associated cellular p300 transcriptional co-activator protein. It functions as histone acetyltransferase that regulates transcription via chromatin remodeling and is important in the processes of cell proliferation and differentiation. It mediates cAMP-gene regulation by binding specifically to phosphorylated CREB protein. This gene has also been identified as a co-activator of HIF1A (hypoxia-inducible factor 1 alpha), and thus plays a role in the stimulation of hypoxia-induced genes such as VEGF. Defects in this gene are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer. [provided by RefSeq, Jul 2008]","start":41091786,"end":41180079,"strand":1,"description":"E1A binding protein p300 [Source:HGNC Symbol;Acc:HGNC:3373]"}, {"versioned_ensembl_gene_id":"ENSG00000280204.3","gene_symbol":"OR1S1","gene_name":"olfactory receptor family 1 subfamily S member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8227]","synonyms":"OST034","biotype":"polymorphic_pseudogene","ncbi_id":"219959","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":58212720,"end":58216084,"strand":1,"description":"olfactory receptor family 1 subfamily S member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8227]"}, {"versioned_ensembl_gene_id":"ENSG00000166526.16","gene_symbol":"ZNF3","gene_name":"zinc finger protein 3 [Source:HGNC Symbol;Acc:HGNC:13089]","synonyms":"Zfp113,PP838,KOX25,HF.12,FLJ20216,A8-51","biotype":"protein_coding","ncbi_id":"7551","summary":null,"start":100064033,"end":100082548,"strand":-1,"description":"zinc finger protein 3 [Source:HGNC Symbol;Acc:HGNC:13089]"}, {"versioned_ensembl_gene_id":"ENSG00000158321.15","gene_symbol":"AUTS2","gene_name":"AUTS2, activator of transcription and developmental regulator [Source:HGNC Symbol;Acc:HGNC:14262]","synonyms":"KIAA0442,FBRSL2","biotype":"protein_coding","ncbi_id":"26053","summary":"This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2014]","start":69598919,"end":70793068,"strand":1,"description":"AUTS2, activator of transcription and developmental regulator [Source:HGNC Symbol;Acc:HGNC:14262]"}, {"versioned_ensembl_gene_id":"ENSG00000051009.10","gene_symbol":"FAM160A2","gene_name":"family with sequence similarity 160 member A2 [Source:HGNC Symbol;Acc:HGNC:25378]","synonyms":"KIAA1759,FLJ22665,FHIP,DKFZP566M1046,C11orf56","biotype":"protein_coding","ncbi_id":"84067","summary":"The protein encoded by this gene is part of the FTS/Hook/FHIP (FHF) complex, which can interact with members of the homotypic vesicular protein sorting (HOPS) complex. This interaction suggests that the encoded protein is involved in vesicle trafficking. [provided by RefSeq, Dec 2016]","start":6211335,"end":6234711,"strand":-1,"description":"family with sequence similarity 160 member A2 [Source:HGNC Symbol;Acc:HGNC:25378]"}, {"versioned_ensembl_gene_id":"ENSG00000235600.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":30049251,"end":30050914,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000253286.5","gene_symbol":"AC090193.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123614225,"end":123658570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133703.11","gene_symbol":"KRAS","gene_name":"KRAS proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:6407]","synonyms":"KRAS2,KRAS1","biotype":"protein_coding","ncbi_id":"3845","summary":"This gene, a Kirsten ras oncogene homolog from the mammalian ras gene family, encodes a protein that is a member of the small GTPase superfamily. A single amino acid substitution is responsible for an activating mutation. The transforming protein that results is implicated in various malignancies, including lung adenocarcinoma, mucinous adenoma, ductal carcinoma of the pancreas and colorectal carcinoma. Alternative splicing leads to variants encoding two isoforms that differ in the C-terminal region. [provided by RefSeq, Jul 2008]","start":25204789,"end":25250936,"strand":-1,"description":"KRAS proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:6407]"}, {"versioned_ensembl_gene_id":"ENSG00000151575.14","gene_symbol":"TEX9","gene_name":"testis expressed 9 [Source:HGNC Symbol;Acc:HGNC:29585]","synonyms":null,"biotype":"protein_coding","ncbi_id":"374618","summary":null,"start":56244009,"end":56445997,"strand":1,"description":"testis expressed 9 [Source:HGNC Symbol;Acc:HGNC:29585]"}, {"versioned_ensembl_gene_id":"ENSG00000261823.1","gene_symbol":"AC084782.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56408483,"end":56410186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170542.5","gene_symbol":"SERPINB9","gene_name":"serpin family B member 9 [Source:HGNC Symbol;Acc:HGNC:8955]","synonyms":"PI9,CAP3","biotype":"protein_coding","ncbi_id":"5272","summary":"This gene encodes a member of the serine protease inhibitor family which are also known as serpins. The encoded protein belongs to a subfamily of intracellular serpins. This protein inhibits the activity of the effector molecule granzyme B. Overexpression of this protein may prevent cytotoxic T-lymphocytes from eliminating certain tumor cells. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Mar 2012]","start":2887266,"end":2903280,"strand":-1,"description":"serpin family B member 9 [Source:HGNC Symbol;Acc:HGNC:8955]"}, {"versioned_ensembl_gene_id":"ENSG00000276517.1","gene_symbol":"AL133243.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32526504,"end":32529507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235996.1","gene_symbol":"AL136090.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19212852,"end":19213477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256004.1","gene_symbol":"AC092490.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8678773,"end":8679670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284042.1","gene_symbol":"AC106774.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17528669,"end":17529265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284234.1","gene_symbol":"AC106774.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17525235,"end":17525831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213972.3","gene_symbol":"AL024509.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25272200,"end":25273751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204217.13","gene_symbol":"BMPR2","gene_name":"bone morphogenetic protein receptor type 2 [Source:HGNC Symbol;Acc:HGNC:1078]","synonyms":"T-ALK,PPH1,BRK-3,BMPR3,BMPR-II","biotype":"protein_coding","ncbi_id":"659","summary":"This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disease. [provided by RefSeq, May 2020]","start":202376936,"end":202567751,"strand":1,"description":"bone morphogenetic protein receptor type 2 [Source:HGNC Symbol;Acc:HGNC:1078]"}, {"versioned_ensembl_gene_id":"ENSG00000211692.1","gene_symbol":"TRGJP1","gene_name":"T-cell receptor gamma joining P1 [Source:HGNC Symbol;Acc:HGNC:12280]","synonyms":"TCRGJP1,JP1","biotype":"TR_J_gene","ncbi_id":"6971","summary":null,"start":38276259,"end":38276318,"strand":-1,"description":"T-cell receptor gamma joining P1 [Source:HGNC Symbol;Acc:HGNC:12280]"}, {"versioned_ensembl_gene_id":"ENSG00000256420.1","gene_symbol":"OSBPL9P4","gene_name":"oxysterol binding protein like 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100498661","summary":null,"start":66563967,"end":66569194,"strand":-1,"description":"oxysterol binding protein like 9 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48734]"}, {"versioned_ensembl_gene_id":"ENSG00000130734.9","gene_symbol":"ATG4D","gene_name":"autophagy related 4D cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:20789]","synonyms":"AUTL4,APG4D,APG4-D","biotype":"protein_coding","ncbi_id":"84971","summary":"Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene belongs to the autophagy-related protein 4 (Atg4) family of C54 endopeptidases. Members of this family encode proteins that play a role in the biogenesis of autophagosomes, which sequester the cytosol and organelles for degradation by lysosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":10543895,"end":10553418,"strand":1,"description":"autophagy related 4D cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:20789]"}, {"versioned_ensembl_gene_id":"ENSG00000211687.1","gene_symbol":"TRGJ2","gene_name":"T-cell receptor gamma joining 2 [Source:HGNC Symbol;Acc:HGNC:12278]","synonyms":"TCRGJ2,J2","biotype":"TR_J_gene","ncbi_id":"6969","summary":null,"start":38253380,"end":38253429,"strand":-1,"description":"T-cell receptor gamma joining 2 [Source:HGNC Symbol;Acc:HGNC:12278]"}, {"versioned_ensembl_gene_id":"ENSG00000211690.1","gene_symbol":"TRGJ1","gene_name":"T-cell receptor gamma joining 1 [Source:HGNC Symbol;Acc:HGNC:12277]","synonyms":"TCRGJ1,J1","biotype":"TR_J_gene","ncbi_id":"6968","summary":null,"start":38269491,"end":38269540,"strand":-1,"description":"T-cell receptor gamma joining 1 [Source:HGNC Symbol;Acc:HGNC:12277]"}, {"versioned_ensembl_gene_id":"ENSG00000234559.1","gene_symbol":"AC079776.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129939848,"end":129940217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225693.1","gene_symbol":"LAGE3P1","gene_name":"L antigen family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49909]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646808","summary":null,"start":33019682,"end":33020165,"strand":-1,"description":"L antigen family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49909]"}, {"versioned_ensembl_gene_id":"ENSG00000272341.1","gene_symbol":"AL137003.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16764346,"end":16766883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166394.14","gene_symbol":"CYB5R2","gene_name":"cytochrome b5 reductase 2 [Source:HGNC Symbol;Acc:HGNC:24376]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51700","summary":"The protein encoded by this gene belongs to the flavoprotein pyridine nucleotide cytochrome reductase family of proteins. Cytochrome b-type NAD(P)H oxidoreductases are implicated in many processes including cholesterol biosynthesis, fatty acid desaturation and elongation, and respiratory burst in neutrophils and macrophages. Cytochrome b5 reductases have soluble and membrane-bound forms that are the product of alternative splicing. In animal cells, the membrane-bound form binds to the endoplasmic reticulum, where it is a member of a fatty acid desaturation complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":7665100,"end":7677222,"strand":-1,"description":"cytochrome b5 reductase 2 [Source:HGNC Symbol;Acc:HGNC:24376]"}, {"versioned_ensembl_gene_id":"ENSG00000132561.13","gene_symbol":"MATN2","gene_name":"matrilin 2 [Source:HGNC Symbol;Acc:HGNC:6908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4147","summary":"This gene encodes a member of the von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains five von Willebrand factor A domains. The specific function of this gene has not yet been determined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":97868840,"end":98036716,"strand":1,"description":"matrilin 2 [Source:HGNC Symbol;Acc:HGNC:6908]"}, {"versioned_ensembl_gene_id":"ENSG00000005156.11","gene_symbol":"LIG3","gene_name":"DNA ligase 3 [Source:HGNC Symbol;Acc:HGNC:6600]","synonyms":"LIG2","biotype":"protein_coding","ncbi_id":"3980","summary":"This gene is a member of the DNA ligase family. Each member of this family encodes a protein that catalyzes the joining of DNA ends but they each have a distinct role in DNA metabolism. The protein encoded by this gene is involved in excision repair and is located in both the mitochondria and nucleus, with translation initiation from the upstream start codon allowing for transport to the mitochondria and translation initiation from a downstream start codon allowing for transport to the nucleus. Additionally, alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":34980494,"end":35009743,"strand":1,"description":"DNA ligase 3 [Source:HGNC Symbol;Acc:HGNC:6600]"}, {"versioned_ensembl_gene_id":"ENSG00000166170.9","gene_symbol":"BAG5","gene_name":"BCL2 associated athanogene 5 [Source:HGNC Symbol;Acc:HGNC:941]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9529","summary":"The protein encoded by this gene is a member of the BAG1-related protein family. BAG1 is an anti-apoptotic protein that functions through interactions with a variety of cell apoptosis and growth related proteins including BCL-2, Raf-protein kinase, steroid hormone receptors, growth factor receptors and members of the heat shock protein 70 kDa family. This protein contains a BAG domain near the C-terminus, which could bind and inhibit the chaperone activity of Hsc70/Hsp70. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":103556544,"end":103562831,"strand":-1,"description":"BCL2 associated athanogene 5 [Source:HGNC Symbol;Acc:HGNC:941]"}, {"versioned_ensembl_gene_id":"ENSG00000284552.1","gene_symbol":"AC106774.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17486231,"end":17486829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253966.1","gene_symbol":"AC008514.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170896929,"end":170904461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231622.1","gene_symbol":"RPS29P7","gene_name":"ribosomal protein S29 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36594]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128377","summary":null,"start":65154480,"end":65154650,"strand":1,"description":"ribosomal protein S29 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36594]"}, {"versioned_ensembl_gene_id":"ENSG00000139687.13","gene_symbol":"RB1","gene_name":"RB transcriptional corepressor 1 [Source:HGNC Symbol;Acc:HGNC:9884]","synonyms":"RB,PPP1R130,OSRC","biotype":"protein_coding","ncbi_id":"5925","summary":"The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]","start":48303751,"end":48481986,"strand":1,"description":"RB transcriptional corepressor 1 [Source:HGNC Symbol;Acc:HGNC:9884]"}, {"versioned_ensembl_gene_id":"ENSG00000251666.1","gene_symbol":"ZNF346-IT1","gene_name":"ZNF346 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41423]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480741","summary":null,"start":177051714,"end":177052963,"strand":1,"description":"ZNF346 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41423]"}, {"versioned_ensembl_gene_id":"ENSG00000229280.1","gene_symbol":"EEF1DP6","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644357","summary":null,"start":4175528,"end":4175899,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51456]"}, {"versioned_ensembl_gene_id":"ENSG00000180739.13","gene_symbol":"S1PR5","gene_name":"sphingosine-1-phosphate receptor 5 [Source:HGNC Symbol;Acc:HGNC:14299]","synonyms":"EDG8,Edg-8","biotype":"protein_coding","ncbi_id":"53637","summary":"The lysosphingolipid sphingosine 1-phosphate (S1P) regulates cell proliferation, apoptosis, motility, and neurite retraction. Its actions may be both intracellular as a second messenger and extracellular as a receptor ligand. S1P and the structurally related lysolipid mediator lysophosphatidic acid (LPA) signal cells through a set of G protein-coupled receptors known as EDG receptors. Some EDG receptors (e.g., EDG1; MIM 601974) are S1P receptors; others (e.g., EDG2; MIM 602282) are LPA receptors.[supplied by OMIM, Mar 2008]","start":10512742,"end":10517931,"strand":-1,"description":"sphingosine-1-phosphate receptor 5 [Source:HGNC Symbol;Acc:HGNC:14299]"}, {"versioned_ensembl_gene_id":"ENSG00000258696.1","gene_symbol":"AL359233.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38003113,"end":38004847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237221.1","gene_symbol":"PPEF1-AS1","gene_name":"PPEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40463]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874004","summary":null,"start":18688643,"end":18691604,"strand":-1,"description":"PPEF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40463]"}, {"versioned_ensembl_gene_id":"ENSG00000275861.4","gene_symbol":"TBC1D3I","gene_name":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724862","summary":null,"start":36355285,"end":36366216,"strand":-1,"description":"TBC1 domain family member 3I [Source:HGNC Symbol;Acc:HGNC:32709]"}, {"versioned_ensembl_gene_id":"ENSG00000230298.1","gene_symbol":"AL590068.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30576699,"end":30580182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274619.2","gene_symbol":"CFD","gene_name":"complement factor D [Source:HGNC Symbol;Acc:HGNC:2771]","synonyms":"PFD,DF,ADN","biotype":"protein_coding","ncbi_id":"1675","summary":"This gene encodes a member of the S1, or chymotrypsin, family of serine peptidases. This protease catalyzes the cleavage of factor B, the rate-limiting step of the alternative pathway of complement activation. This protein also functions as an adipokine, a cell signaling protein secreted by adipocytes, which regulates insulin secretion in mice. Mutations in this gene underlie complement factor D deficiency, which is associated with recurrent bacterial meningitis infections in human patients. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature protease. [provided by RefSeq, Nov 2015]","start":859680,"end":863666,"strand":1,"description":"complement factor D [Source:HGNC Symbol;Acc:HGNC:2771]"}, {"versioned_ensembl_gene_id":"ENSG00000236095.1","gene_symbol":"AL807757.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":94900429,"end":94904754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262400.1","gene_symbol":"AL590084.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25152547,"end":25152883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219682.4","gene_symbol":"AL133268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25140003,"end":25141403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010270.13","gene_symbol":"STARD3NL","gene_name":"STARD3 N-terminal like [Source:HGNC Symbol;Acc:HGNC:19169]","synonyms":"MGC3251,MENTHO","biotype":"protein_coding","ncbi_id":"83930","summary":"This gene encodes a late-endosomal protein that contains a conserved MENTAL (MLN64 N-terminal) domain. The encoded protein binds cholesterol molecules and may play a role in endosomal cholesterol transport through interactions with metastatic lymph node protein 64 (MLN64). [provided by RefSeq, Sep 2011]","start":38178222,"end":38230671,"strand":1,"description":"STARD3 N-terminal like [Source:HGNC Symbol;Acc:HGNC:19169]"}, {"versioned_ensembl_gene_id":"ENSG00000108702.3","gene_symbol":"CCL1","gene_name":"C-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10609]","synonyms":"TCA3,SISe,SCYA1,P500,I-309","biotype":"protein_coding","ncbi_id":"6346","summary":"This antimicrobial gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, is secreted by activated T cells and displays chemotactic activity for monocytes but not for neutrophils. It binds to the chemokine (C-C motif) receptor 8. [provided by RefSeq, Sep 2014]","start":34360328,"end":34363231,"strand":-1,"description":"C-C motif chemokine ligand 1 [Source:HGNC Symbol;Acc:HGNC:10609]"}, {"versioned_ensembl_gene_id":"ENSG00000230992.3","gene_symbol":"FAM201B","gene_name":"family with sequence similarity 201 member B [Source:HGNC Symbol;Acc:HGNC:27933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339742","summary":null,"start":132352722,"end":132353318,"strand":1,"description":"family with sequence similarity 201 member B [Source:HGNC Symbol;Acc:HGNC:27933]"}, {"versioned_ensembl_gene_id":"ENSG00000269765.2","gene_symbol":"AC011492.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15515342,"end":15516836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215448.3","gene_symbol":"SRMP1","gene_name":"spermidine synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16552]","synonyms":"dJ1057D4.1","biotype":"processed_pseudogene","ncbi_id":"170552","summary":null,"start":47859788,"end":47860672,"strand":1,"description":"spermidine synthase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16552]"}, {"versioned_ensembl_gene_id":"ENSG00000188365.3","gene_symbol":"AC092171.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5419846,"end":5423122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170271.10","gene_symbol":"FAXDC2","gene_name":"fatty acid hydroxylase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1334]","synonyms":"FLJ13758,C5orf4","biotype":"protein_coding","ncbi_id":"10826","summary":null,"start":154818491,"end":154859252,"strand":-1,"description":"fatty acid hydroxylase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1334]"}, {"versioned_ensembl_gene_id":"ENSG00000231107.1","gene_symbol":"LINC01508","gene_name":"long intergenic non-protein coding RNA 1508 [Source:HGNC Symbol;Acc:HGNC:51190]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927873","summary":null,"start":90300902,"end":90433505,"strand":-1,"description":"long intergenic non-protein coding RNA 1508 [Source:HGNC Symbol;Acc:HGNC:51190]"}, {"versioned_ensembl_gene_id":"ENSG00000217783.2","gene_symbol":"LDHAL6FP","gene_name":"lactate dehydrogenase A like 6F, pseudogene [Source:HGNC Symbol;Acc:HGNC:44240]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420477","summary":null,"start":157299045,"end":157300126,"strand":-1,"description":"lactate dehydrogenase A like 6F, pseudogene [Source:HGNC Symbol;Acc:HGNC:44240]"}, {"versioned_ensembl_gene_id":"ENSG00000246477.3","gene_symbol":"AF131216.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11315859,"end":11325429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277438.1","gene_symbol":"KDM5DP1","gene_name":"lysine demethylase 5D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23976]","synonyms":"SMCYP","biotype":"processed_pseudogene","ncbi_id":"359796","summary":null,"start":20570222,"end":20570519,"strand":-1,"description":"lysine demethylase 5D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23976]"}, {"versioned_ensembl_gene_id":"ENSG00000085662.13","gene_symbol":"AKR1B1","gene_name":"aldo-keto reductase family 1 member B [Source:HGNC Symbol;Acc:HGNC:381]","synonyms":"AR,ALDR1","biotype":"protein_coding","ncbi_id":"231","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. This member catalyzes the reduction of a number of aldehydes, including the aldehyde form of glucose, and is thereby implicated in the development of diabetic complications by catalyzing the reduction of glucose to sorbitol. Multiple pseudogenes have been identified for this gene. The nomenclature system used by the HUGO Gene Nomenclature Committee to define human aldo-keto reductase family members is known to differ from that used by the Mouse Genome Informatics database. [provided by RefSeq, Feb 2009]","start":134442350,"end":134459284,"strand":-1,"description":"aldo-keto reductase family 1 member B [Source:HGNC Symbol;Acc:HGNC:381]"}, {"versioned_ensembl_gene_id":"ENSG00000136156.12","gene_symbol":"ITM2B","gene_name":"integral membrane protein 2B [Source:HGNC Symbol;Acc:HGNC:6174]","synonyms":"E3-16,E25B,BRICD2B,BRI2,BRI","biotype":"protein_coding","ncbi_id":"9445","summary":"Amyloid precursor proteins are processed by beta-secretase and gamma-secretase to produce beta-amyloid peptides which form the characteristic plaques of Alzheimer disease. This gene encodes a transmembrane protein which is processed at the C-terminus by furin or furin-like proteases to produce a small secreted peptide which inhibits the deposition of beta-amyloid. Mutations which result in extension of the C-terminal end of the encoded protein, thereby increasing the size of the secreted peptide, are associated with two neurogenerative diseases, familial British dementia and familial Danish dementia. [provided by RefSeq, Oct 2009]","start":48233158,"end":48270357,"strand":1,"description":"integral membrane protein 2B [Source:HGNC Symbol;Acc:HGNC:6174]"}, {"versioned_ensembl_gene_id":"ENSG00000236839.1","gene_symbol":"AC069280.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69187833,"end":69189318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229715.4","gene_symbol":"EEF1DP3","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30486]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"196549","summary":null,"start":31846841,"end":31953472,"strand":1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30486]"}, {"versioned_ensembl_gene_id":"ENSG00000211454.13","gene_symbol":"AKR7L","gene_name":"aldo-keto reductase family 7 like (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:24056]","synonyms":"AFAR3","biotype":"polymorphic_pseudogene","ncbi_id":"246181","summary":"This gene is one of three aldo-keto reductase genes that are present in a cluster on the p arm of chromosome 1. The encoded proteins are involved in the reduction of the dialdehyde protein-binding form of aflatoxin B1 (AFB1) to the non-binding AFB1 dialcohol. It has been speculated that this family member encodes a selenoprotein, which includes a selenocysteine (Sec) residue in lieu of a UGA translational termination codon. However, there is no evidence that such a protein is produced in vivo. The alternative interpretation is that this family member is a segregating pseudogene, where some individuals have an allele that encodes a functional enzyme, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Feb 2017]","start":19265982,"end":19274194,"strand":-1,"description":"aldo-keto reductase family 7 like (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:24056]"}, {"versioned_ensembl_gene_id":"ENSG00000087258.14","gene_symbol":"GNAO1","gene_name":"G protein subunit alpha o1 [Source:HGNC Symbol;Acc:HGNC:4389]","synonyms":"G-ALPHA-o","biotype":"protein_coding","ncbi_id":"2775","summary":"The protein encoded by this gene represents the alpha subunit of the Go heterotrimeric G-protein signal-transducing complex. Defects in this gene are a cause of early-onset epileptic encephalopathy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":56191347,"end":56357457,"strand":1,"description":"G protein subunit alpha o1 [Source:HGNC Symbol;Acc:HGNC:4389]"}, {"versioned_ensembl_gene_id":"ENSG00000231123.1","gene_symbol":"SPATA20P1","gene_name":"spermatogenesis associated 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39636]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874060","summary":null,"start":38238227,"end":38238664,"strand":-1,"description":"spermatogenesis associated 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39636]"}, {"versioned_ensembl_gene_id":"ENSG00000279764.1","gene_symbol":"AC009102.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56306845,"end":56308335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261439.1","gene_symbol":"DKFZP434H168","gene_name":"uncharacterized LOC26077 [Source:NCBI gene;Acc:26077]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"26077","summary":null,"start":56192614,"end":56194518,"strand":-1,"description":"uncharacterized LOC26077 [Source:NCBI gene;Acc:26077]"}, {"versioned_ensembl_gene_id":"ENSG00000260198.1","gene_symbol":"AC009102.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56300616,"end":56302904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182348.6","gene_symbol":"ZNF804B","gene_name":"zinc finger protein 804B [Source:HGNC Symbol;Acc:HGNC:21958]","synonyms":"FLJ32110","biotype":"protein_coding","ncbi_id":"219578","summary":null,"start":88759368,"end":89337057,"strand":1,"description":"zinc finger protein 804B [Source:HGNC Symbol;Acc:HGNC:21958]"}, {"versioned_ensembl_gene_id":"ENSG00000227550.2","gene_symbol":"TRBV7-5","gene_name":"T-cell receptor beta variable 7-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12239]","synonyms":"TCRBV7S5,TCRBV6S9P,TRBV75","biotype":"TR_V_pseudogene","ncbi_id":"28593","summary":null,"start":142474096,"end":142474567,"strand":1,"description":"T-cell receptor beta variable 7-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12239]"}, {"versioned_ensembl_gene_id":"ENSG00000228814.4","gene_symbol":"AC017007.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":112881718,"end":112882132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271298.1","gene_symbol":"AL080274.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11838355,"end":11838574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184388.5","gene_symbol":"PABPC1L2B","gene_name":"poly(A) binding protein cytoplasmic 1 like 2B [Source:HGNC Symbol;Acc:HGNC:31852]","synonyms":"RBM32B","biotype":"protein_coding","ncbi_id":"645974","summary":null,"start":73003517,"end":73005713,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 like 2B [Source:HGNC Symbol;Acc:HGNC:31852]"}, {"versioned_ensembl_gene_id":"ENSG00000168118.11","gene_symbol":"RAB4A","gene_name":"RAB4A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9781]","synonyms":"RAB4,HRES-1/RAB4","biotype":"protein_coding","ncbi_id":"5867","summary":"This gene is a member of the largest group in the Ras superfamily of small GTPases, which regulate membrane trafficking. The encoded protein is associated with early endosomes and is involved in their sorting and recycling. The protein also plays a role in regulating the recycling of receptors from endosomes to the plasma membrane. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2012]","start":229271062,"end":229305894,"strand":1,"description":"RAB4A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9781]"}, {"versioned_ensembl_gene_id":"ENSG00000114395.10","gene_symbol":"CYB561D2","gene_name":"cytochrome b561 family member D2 [Source:HGNC Symbol;Acc:HGNC:30253]","synonyms":"TSP10,101F6,XXcos-LUCA11.4,TSP10,101F6","biotype":"protein_coding","ncbi_id":"11068","summary":null,"start":50350695,"end":50358460,"strand":1,"description":"cytochrome b561 family member D2 [Source:HGNC Symbol;Acc:HGNC:30253]"}, {"versioned_ensembl_gene_id":"ENSG00000278486.1","gene_symbol":"YRDCP1","gene_name":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420501","summary":null,"start":94432631,"end":94433273,"strand":-1,"description":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39919]"}, {"versioned_ensembl_gene_id":"ENSG00000232400.1","gene_symbol":"RAD17P1","gene_name":"RAD17 checkpoint clamp loader component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9808]","synonyms":"HRAD17P1","biotype":"processed_pseudogene","ncbi_id":"9207","summary":null,"start":16864267,"end":16866308,"strand":-1,"description":"RAD17 checkpoint clamp loader component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9808]"}, {"versioned_ensembl_gene_id":"ENSG00000136854.19","gene_symbol":"STXBP1","gene_name":"syntaxin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11444]","synonyms":"rbSec1,MUNC18-1,hUNC18,UNC18","biotype":"protein_coding","ncbi_id":"6812","summary":"This gene encodes a syntaxin-binding protein. The encoded protein appears to play a role in release of neurotransmitters via regulation of syntaxin, a transmembrane attachment protein receptor. Mutations in this gene have been associated with infantile epileptic encephalopathy-4. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]","start":127579370,"end":127696027,"strand":1,"description":"syntaxin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11444]"}, {"versioned_ensembl_gene_id":"ENSG00000282319.1","gene_symbol":"AC131056.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36282949,"end":36284006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177788.5","gene_symbol":"AL162595.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":229258281,"end":229271028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234644.2","gene_symbol":"OTX2P1","gene_name":"orthodenticle homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33281]","synonyms":"OTX2P","biotype":"processed_pseudogene","ncbi_id":"100033409","summary":null,"start":75724222,"end":75724575,"strand":-1,"description":"orthodenticle homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33281]"}, {"versioned_ensembl_gene_id":"ENSG00000232698.1","gene_symbol":"AP001058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44206525,"end":44207399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242616.3","gene_symbol":"GNG10","gene_name":"G protein subunit gamma 10 [Source:HGNC Symbol;Acc:HGNC:4402]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2790","summary":null,"start":111661335,"end":111670246,"strand":1,"description":"G protein subunit gamma 10 [Source:HGNC Symbol;Acc:HGNC:4402]"}, {"versioned_ensembl_gene_id":"ENSG00000224895.1","gene_symbol":"VPS26BP1","gene_name":"VPS26B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421729","summary":null,"start":47960327,"end":47961081,"strand":-1,"description":"VPS26B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44612]"}, {"versioned_ensembl_gene_id":"ENSG00000125246.15","gene_symbol":"CLYBL","gene_name":"citrate lyase beta like [Source:HGNC Symbol;Acc:HGNC:18355]","synonyms":"CLB","biotype":"protein_coding","ncbi_id":"171425","summary":null,"start":99606669,"end":99897134,"strand":1,"description":"citrate lyase beta like [Source:HGNC Symbol;Acc:HGNC:18355]"}, {"versioned_ensembl_gene_id":"ENSG00000233560.2","gene_symbol":"KRT8P39","gene_name":"keratin 8 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39873]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418781","summary":null,"start":68705634,"end":68707066,"strand":1,"description":"keratin 8 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39873]"}, {"versioned_ensembl_gene_id":"ENSG00000254264.2","gene_symbol":"IGKV3OR22-2","gene_name":"immunoglobulin kappa variable 3/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5833]","synonyms":"IGKVP3,IGKV3/OR22-2","biotype":"IG_V_pseudogene","ncbi_id":"3527","summary":null,"start":16925952,"end":16926444,"strand":-1,"description":"immunoglobulin kappa variable 3/OR22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5833]"}, {"versioned_ensembl_gene_id":"ENSG00000248772.1","gene_symbol":"AC108729.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155375683,"end":155375790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135525.18","gene_symbol":"MAP7","gene_name":"microtubule associated protein 7 [Source:HGNC Symbol;Acc:HGNC:6869]","synonyms":"E-MAP-115","biotype":"protein_coding","ncbi_id":"9053","summary":"The product of this gene is a microtubule-associated protein that is predominantly expressed in cells of epithelial origin. Microtubule-associated proteins are thought to be involved in microtubule dynamics, which is essential for cell polarization and differentiation. This protein has been shown to be able to stabilize microtubules, and may serve to modulate microtubule functions. Studies of the related mouse protein also suggested an essential role in microtubule function required for spermatogenesis. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":136342281,"end":136550819,"strand":-1,"description":"microtubule associated protein 7 [Source:HGNC Symbol;Acc:HGNC:6869]"}, {"versioned_ensembl_gene_id":"ENSG00000077984.5","gene_symbol":"CST7","gene_name":"cystatin F [Source:HGNC Symbol;Acc:HGNC:2479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8530","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. This gene encodes a glycosylated cysteine protease inhibitor with a putative role in immune regulation through inhibition of a unique target in the hematopoietic system. Expression of the protein has been observed in various human cancer cell lines established from malignant tumors. [provided by RefSeq, Jul 2008]","start":24949230,"end":24959928,"strand":1,"description":"cystatin F [Source:HGNC Symbol;Acc:HGNC:2479]"}, {"versioned_ensembl_gene_id":"ENSG00000175416.12","gene_symbol":"CLTB","gene_name":"clathrin light chain B [Source:HGNC Symbol;Acc:HGNC:2091]","synonyms":"Lcb","biotype":"protein_coding","ncbi_id":"1212","summary":"Clathrin is a large, soluble protein composed of heavy and light chains. It functions as the main structural component of the lattice-type cytoplasmic face of coated pits and vesicles which entrap specific macromolecules during receptor-mediated endocytosis. This gene encodes one of two clathrin light chain proteins which are believed to function as regulatory elements. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":176392455,"end":176416569,"strand":-1,"description":"clathrin light chain B [Source:HGNC Symbol;Acc:HGNC:2091]"}, {"versioned_ensembl_gene_id":"ENSG00000269433.3","gene_symbol":"OPN1MW3","gene_name":"opsin 1, medium wave sensitive 3 [Source:HGNC Symbol;Acc:HGNC:51831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060233","summary":null,"start":154257538,"end":154271805,"strand":1,"description":"opsin 1, medium wave sensitive 3 [Source:HGNC Symbol;Acc:HGNC:51831]"}, {"versioned_ensembl_gene_id":"ENSG00000115648.13","gene_symbol":"MLPH","gene_name":"melanophilin [Source:HGNC Symbol;Acc:HGNC:29643]","synonyms":"ln,l1Rk3,l(1)-3Rk,exophilin-3,Slac-2a","biotype":"protein_coding","ncbi_id":"79083","summary":"This gene encodes a member of the exophilin subfamily of Rab effector proteins. The protein forms a ternary complex with the small Ras-related GTPase Rab27A in its GTP-bound form and the motor protein myosin Va. A similar protein complex in mouse functions to tether pigment-producing organelles called melanosomes to the actin cytoskeleton in melanocytes, and is required for visible pigmentation in the hair and skin. A mutation in this gene results in Griscelli syndrome type 3, which is characterized by a silver-gray hair color and abnormal pigment distribution in the hair shaft. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":237485428,"end":237555318,"strand":1,"description":"melanophilin [Source:HGNC Symbol;Acc:HGNC:29643]"}, {"versioned_ensembl_gene_id":"ENSG00000223987.1","gene_symbol":"RPL26P28","gene_name":"ribosomal protein L26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130983","summary":null,"start":5304431,"end":5304865,"strand":-1,"description":"ribosomal protein L26 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35776]"}, {"versioned_ensembl_gene_id":"ENSG00000089053.12","gene_symbol":"ANAPC5","gene_name":"anaphase promoting complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:15713]","synonyms":"APC5","biotype":"protein_coding","ncbi_id":"51433","summary":"This gene encodes a tetratricopeptide repeat-containing component of the anaphase promoting complex/cyclosome (APC/C), a large E3 ubiquitin ligase that controls cell cycle progression by targeting a number of cell cycle regulators such as B-type cyclins for 26S proteasome-mediated degradation through ubiquitination. The encoded protein is required for the proper ubiquitination function of APC/C and for the interaction of APC/C with transcription coactivators. It also interacts with polyA binding protein and represses internal ribosome entry site-mediated translation. Multiple transcript variants encoding different isoforms have been found for this gene. These differences cause translation initiation at a downstream AUG and result in a shorter protein (isoform b), compared to isoform a. [provided by RefSeq, Nov 2008]","start":121308245,"end":121399896,"strand":-1,"description":"anaphase promoting complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:15713]"}, {"versioned_ensembl_gene_id":"ENSG00000114062.18","gene_symbol":"UBE3A","gene_name":"ubiquitin protein ligase E3A [Source:HGNC Symbol;Acc:HGNC:12496]","synonyms":"FLJ26981,EPVE6AP,E6-AP,AS,ANCR,HPVE6A","biotype":"protein_coding","ncbi_id":"7337","summary":"This gene encodes an E3 ubiquitin-protein ligase, part of the ubiquitin protein degradation system. This imprinted gene is maternally expressed in brain and biallelically expressed in other tissues. Maternally inherited deletion of this gene causes Angelman Syndrome, characterized by severe motor and intellectual retardation, ataxia, hypotonia, epilepsy, absence of speech, and characteristic facies. The protein also interacts with the E6 protein of human papillomavirus types 16 and 18, resulting in ubiquitination and proteolysis of tumor protein p53. Alternative splicing of this gene results in three transcript variants encoding three isoforms with different N-termini. Additional transcript variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":25333728,"end":25439056,"strand":-1,"description":"ubiquitin protein ligase E3A [Source:HGNC Symbol;Acc:HGNC:12496]"}, {"versioned_ensembl_gene_id":"ENSG00000253581.1","gene_symbol":"AC105031.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82979411,"end":82979886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259062.2","gene_symbol":"ACTN1-AS1","gene_name":"ACTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20131]","synonyms":"C14orf84","biotype":"antisense_RNA","ncbi_id":"161159","summary":null,"start":68979682,"end":68987463,"strand":1,"description":"ACTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20131]"}, {"versioned_ensembl_gene_id":"ENSG00000242736.1","gene_symbol":"TRBV1","gene_name":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]","synonyms":"TCRBV27S1P,TCRBV1S1P","biotype":"TR_V_pseudogene","ncbi_id":"28621","summary":null,"start":142299177,"end":142299460,"strand":1,"description":"T-cell receptor beta variable 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12176]"}, {"versioned_ensembl_gene_id":"ENSG00000253729.7","gene_symbol":"PRKDC","gene_name":"protein kinase, DNA-activated, catalytic polypeptide [Source:HGNC Symbol;Acc:HGNC:9413]","synonyms":"p350,HYRC1,HYRC,DNPK1,DNAPK,DNA-PKcs,XRCC7","biotype":"protein_coding","ncbi_id":"5591","summary":"This gene encodes the catalytic subunit of the DNA-dependent protein kinase (DNA-PK). It functions with the Ku70/Ku80 heterodimer protein in DNA double strand break repair and recombination. The protein encoded is a member of the PI3/PI4-kinase family.[provided by RefSeq, Jul 2010]","start":47773108,"end":47960183,"strand":-1,"description":"protein kinase, DNA-activated, catalytic polypeptide [Source:HGNC Symbol;Acc:HGNC:9413]"}, {"versioned_ensembl_gene_id":"ENSG00000230705.4","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32878685,"end":32887454,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000237689.1","gene_symbol":"AC007064.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16869478,"end":16871126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196166.3","gene_symbol":"C8orf86","gene_name":"chromosome 8 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:33774]","synonyms":"FLJ43582","biotype":"protein_coding","ncbi_id":"389649","summary":null,"start":38510834,"end":38528662,"strand":-1,"description":"chromosome 8 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:33774]"}, {"versioned_ensembl_gene_id":"ENSG00000007866.19","gene_symbol":"TEAD3","gene_name":"TEA domain transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11716]","synonyms":"TEF-5,TEAD5,ETFR-1","biotype":"protein_coding","ncbi_id":"7005","summary":"This gene product is a member of the transcriptional enhancer factor (TEF) family of transcription factors, which contain the TEA/ATTS DNA-binding domain. It is predominantly expressed in the placenta and is involved in the transactivation of the chorionic somatomammotropin-B gene enhancer. Translation of this protein is initiated at a non-AUG (AUA) start codon. [provided by RefSeq, Jul 2008]","start":35473597,"end":35497076,"strand":-1,"description":"TEA domain transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:11716]"}, {"versioned_ensembl_gene_id":"ENSG00000275029.1","gene_symbol":"HMGB1P24","gene_name":"high mobility group box 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39115]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100420063","summary":null,"start":37143607,"end":37144463,"strand":-1,"description":"high mobility group box 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39115]"}, {"versioned_ensembl_gene_id":"ENSG00000283535.1","gene_symbol":"AC007064.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16844399,"end":16846357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233498.8","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"IPP-2P,PPP1R2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32912612,"end":32913288,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000228476.1","gene_symbol":"CSTP1","gene_name":"cystatin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2486]","synonyms":"dJ850N15.1","biotype":"unprocessed_pseudogene","ncbi_id":"1480","summary":null,"start":23918771,"end":23922169,"strand":-1,"description":"cystatin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2486]"}, {"versioned_ensembl_gene_id":"ENSG00000249601.2","gene_symbol":"LINC01187","gene_name":"long intergenic non-protein coding RNA 1187 [Source:HGNC Symbol;Acc:HGNC:49575]","synonyms":"KIDR","biotype":"lincRNA","ncbi_id":"100507267","summary":null,"start":170191579,"end":170199141,"strand":-1,"description":"long intergenic non-protein coding RNA 1187 [Source:HGNC Symbol;Acc:HGNC:49575]"}, {"versioned_ensembl_gene_id":"ENSG00000265775.1","gene_symbol":"AC004147.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34118347,"end":34118882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103316.10","gene_symbol":"CRYM","gene_name":"crystallin mu [Source:HGNC Symbol;Acc:HGNC:2418]","synonyms":"DFNA40","biotype":"protein_coding","ncbi_id":"1428","summary":"Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness. [provided by RefSeq, Sep 2014]","start":21238874,"end":21303083,"strand":-1,"description":"crystallin mu [Source:HGNC Symbol;Acc:HGNC:2418]"}, {"versioned_ensembl_gene_id":"ENSG00000187122.16","gene_symbol":"SLIT1","gene_name":"slit guidance ligand 1 [Source:HGNC Symbol;Acc:HGNC:11085]","synonyms":"SLIT3,slit1,Slit-1,SLIL1,MEGF4","biotype":"protein_coding","ncbi_id":"6585","summary":null,"start":96998038,"end":97185920,"strand":-1,"description":"slit guidance ligand 1 [Source:HGNC Symbol;Acc:HGNC:11085]"}, {"versioned_ensembl_gene_id":"ENSG00000251667.1","gene_symbol":"BRCC3P1","gene_name":"BRCA1/BRCA2-containing complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51444]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421311","summary":null,"start":176308063,"end":176309013,"strand":1,"description":"BRCA1/BRCA2-containing complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51444]"}, {"versioned_ensembl_gene_id":"ENSG00000213390.10","gene_symbol":"ARHGAP19","gene_name":"Rho GTPase activating protein 19 [Source:HGNC Symbol;Acc:HGNC:23724]","synonyms":"MGC14258,FLJ00194","biotype":"protein_coding","ncbi_id":"84986","summary":"Members of the ARHGAP family, such as ARHGAP19, encode negative regulators of Rho GTPases (see RHOA; MIM 165390), which are involved in cell migration, proliferation, and differentiation, actin remodeling, and G1 cell cycle progression (Lv et al., 2007 [PubMed 17454002]).[supplied by OMIM, Mar 2008]","start":97222173,"end":97292673,"strand":-1,"description":"Rho GTPase activating protein 19 [Source:HGNC Symbol;Acc:HGNC:23724]"}, {"versioned_ensembl_gene_id":"ENSG00000261882.1","gene_symbol":"AC006600.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56368063,"end":56368215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241061.3","gene_symbol":"RPL5P1","gene_name":"ribosomal protein L5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647436","summary":null,"start":24908932,"end":24909825,"strand":-1,"description":"ribosomal protein L5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10361]"}, {"versioned_ensembl_gene_id":"ENSG00000270792.5","gene_symbol":"AL050403.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10672928,"end":10994924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224961.1","gene_symbol":"LINC01752","gene_name":"long intergenic non-protein coding RNA 1752 [Source:HGNC Symbol;Acc:HGNC:52540]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929395","summary":null,"start":10753090,"end":10753966,"strand":1,"description":"long intergenic non-protein coding RNA 1752 [Source:HGNC Symbol;Acc:HGNC:52540]"}, {"versioned_ensembl_gene_id":"ENSG00000143126.7","gene_symbol":"CELSR2","gene_name":"cadherin EGF LAG seven-pass G-type receptor 2 [Source:HGNC Symbol;Acc:HGNC:3231]","synonyms":"MEGF3,KIAA0279,Flamingo1,EGFL2,CDHF10,ADGRC2","biotype":"protein_coding","ncbi_id":"1952","summary":"The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. The specific function of this particular member has not been determined. [provided by RefSeq, Jul 2008]","start":109250019,"end":109275750,"strand":1,"description":"cadherin EGF LAG seven-pass G-type receptor 2 [Source:HGNC Symbol;Acc:HGNC:3231]"}, {"versioned_ensembl_gene_id":"ENSG00000055044.10","gene_symbol":"NOP58","gene_name":"NOP58 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:29926]","synonyms":"NOP5,HSPC120","biotype":"protein_coding","ncbi_id":"51602","summary":"The protein encoded by this gene is a core component of box C/D small nucleolar ribonucleoproteins. Some box C/D small nucleolar RNAs (snoRNAs), such as U3, U8, and U14, are dependent upon the encoded protein for their synthesis. This protein is SUMOylated, which is necessary for high affinity binding to snoRNAs. [provided by RefSeq, Nov 2015]","start":202265716,"end":202303666,"strand":1,"description":"NOP58 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:29926]"}, {"versioned_ensembl_gene_id":"ENSG00000241526.1","gene_symbol":"AC112771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141724425,"end":141724526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131914.10","gene_symbol":"LIN28A","gene_name":"lin-28 homolog A [Source:HGNC Symbol;Acc:HGNC:15986]","synonyms":"ZCCHC1,LIN28,LIN-28,FLJ12457,CSDD1","biotype":"protein_coding","ncbi_id":"79727","summary":"This gene encodes a LIN-28 family RNA-binding protein that acts as a posttranscriptional regulator of genes involved in developmental timing and self-renewal in embryonic stem cells. The encoded protein functions through direct interaction with target mRNAs and by disrupting the maturation of certain miRNAs involved in embryonic development. This protein prevents the terminal processing of the LET7 family of microRNAs which are major regulators of cellular growth and differentiation. Aberrant expression of this gene is associated with cancer progression in multiple tissues. [provided by RefSeq, Sep 2015]","start":26410778,"end":26429722,"strand":1,"description":"lin-28 homolog A [Source:HGNC Symbol;Acc:HGNC:15986]"}, {"versioned_ensembl_gene_id":"ENSG00000283406.1","gene_symbol":"DGCR5","gene_name":"DiGeorge syndrome critical region gene 5 (non-protein coding) [Source:NCBI gene;Acc:26220]","synonyms":"NCRNA00037,LINC00037,NCRNA00037,LINC00037","biotype":"processed_transcript","ncbi_id":"26220","summary":null,"start":18970525,"end":19031242,"strand":1,"description":"DiGeorge syndrome critical region gene 5 (non-protein coding) [Source:NCBI gene;Acc:26220]"}, {"versioned_ensembl_gene_id":"ENSG00000266171.1","gene_symbol":"AP001020.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":735746,"end":737459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258135.5","gene_symbol":"LINC02396","gene_name":"long intergenic non-protein coding RNA 2396 [Source:HGNC Symbol;Acc:HGNC:27463]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283332","summary":null,"start":49908882,"end":49911863,"strand":-1,"description":"long intergenic non-protein coding RNA 2396 [Source:HGNC Symbol;Acc:HGNC:27463]"}, {"versioned_ensembl_gene_id":"ENSG00000237517.9","gene_symbol":"DGCR5","gene_name":"DiGeorge syndrome critical region gene 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16757]","synonyms":"NCRNA00037,LINC00037,NCRNA00037,LINC00037","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26220","summary":null,"start":18970514,"end":18994628,"strand":1,"description":"DiGeorge syndrome critical region gene 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16757]"}, {"versioned_ensembl_gene_id":"ENSG00000228819.1","gene_symbol":"AL049792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132130091,"end":132131352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214975.4","gene_symbol":"PPIAP29","gene_name":"peptidylprolyl isomerase A pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:43021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"134997","summary":null,"start":24976419,"end":24976982,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:43021]"}, {"versioned_ensembl_gene_id":"ENSG00000166111.9","gene_symbol":"SVOP","gene_name":"SV2 related protein [Source:HGNC Symbol;Acc:HGNC:25417]","synonyms":"DKFZp761H039","biotype":"protein_coding","ncbi_id":"55530","summary":null,"start":108907741,"end":109021240,"strand":-1,"description":"SV2 related protein [Source:HGNC Symbol;Acc:HGNC:25417]"}, {"versioned_ensembl_gene_id":"ENSG00000135205.14","gene_symbol":"CCDC146","gene_name":"coiled-coil domain containing 146 [Source:HGNC Symbol;Acc:HGNC:29296]","synonyms":"KIAA1505","biotype":"protein_coding","ncbi_id":"57639","summary":null,"start":77122434,"end":77329533,"strand":1,"description":"coiled-coil domain containing 146 [Source:HGNC Symbol;Acc:HGNC:29296]"}, {"versioned_ensembl_gene_id":"ENSG00000229313.1","gene_symbol":"AL133268.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25041839,"end":25056664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223623.1","gene_symbol":"AL133268.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25053627,"end":25057073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021300.13","gene_symbol":"PLEKHB1","gene_name":"pleckstrin homology domain containing B1 [Source:HGNC Symbol;Acc:HGNC:19079]","synonyms":"PHRET1,PHR1,KPL1","biotype":"protein_coding","ncbi_id":"58473","summary":null,"start":73646178,"end":73662819,"strand":1,"description":"pleckstrin homology domain containing B1 [Source:HGNC Symbol;Acc:HGNC:19079]"}, {"versioned_ensembl_gene_id":"ENSG00000117983.17","gene_symbol":"MUC5B","gene_name":"mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7516]","synonyms":"MUC5,MG1","biotype":"protein_coding","ncbi_id":"727897","summary":"This gene encodes a member of the mucin family of proteins, which are highly glycosylated macromolecular components of mucus secretions. This family member is the major gel-forming mucin in mucus. It is a major contributor to the lubricating and viscoelastic properties of whole saliva, normal lung mucus and cervical mucus. This gene has been found to be up-regulated in some human diseases, including sinus mucosa of chronic rhinosinusitis (CRS), CRS with nasal polyposis, chronic obstructive pulmonary disease (COPD) and H. pylori-associated gastric disease, and it may be involved in the pathogenesis of these diseases. [provided by RefSeq, Jul 2010]","start":1223066,"end":1262172,"strand":1,"description":"mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7516]"}, {"versioned_ensembl_gene_id":"ENSG00000226900.1","gene_symbol":"AL451069.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132511626,"end":132518191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233318.2","gene_symbol":"RPL31P45","gene_name":"ribosomal protein L31 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36796]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729308","summary":null,"start":22266991,"end":22267346,"strand":1,"description":"ribosomal protein L31 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36796]"}, {"versioned_ensembl_gene_id":"ENSG00000258654.1","gene_symbol":"AC026495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20344736,"end":20359166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182934.11","gene_symbol":"SRPRA","gene_name":"SRP receptor alpha subunit [Source:HGNC Symbol;Acc:HGNC:11307]","synonyms":"SRP-alpha,Sralpha,SR-alpha,SRPR","biotype":"protein_coding","ncbi_id":"6734","summary":"The gene encodes a subunit of the endoplasmic reticulum signal recognition particle receptor that, in conjunction with the signal recognition particle, is involved in the targeting and translocation of signal sequence tagged secretory and membrane proteins across the endoplasmic reticulum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":126262919,"end":126269144,"strand":-1,"description":"SRP receptor alpha subunit [Source:HGNC Symbol;Acc:HGNC:11307]"}, {"versioned_ensembl_gene_id":"ENSG00000277742.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786355,"end":54790318,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000249777.1","gene_symbol":"SAP18P1","gene_name":"SAP18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51567]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480689","summary":null,"start":76075531,"end":76075920,"strand":1,"description":"SAP18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51567]"}, {"versioned_ensembl_gene_id":"ENSG00000226853.2","gene_symbol":"AC010894.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174487389,"end":174488386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246145.1","gene_symbol":"RRS1-AS1","gene_name":"RRS1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50465]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505676","summary":null,"start":66419589,"end":66428977,"strand":-1,"description":"RRS1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50465]"}, {"versioned_ensembl_gene_id":"ENSG00000061794.12","gene_symbol":"MRPS35","gene_name":"mitochondrial ribosomal protein S35 [Source:HGNC Symbol;Acc:HGNC:16635]","synonyms":"MRPS28,MDS023","biotype":"protein_coding","ncbi_id":"60488","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that has had confusing nomenclature in the literature. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Pseudogenes corresponding to this gene are found on chromosomes 3p, 5q, and 10q. [provided by RefSeq, Jul 2010]","start":27710773,"end":27756295,"strand":1,"description":"mitochondrial ribosomal protein S35 [Source:HGNC Symbol;Acc:HGNC:16635]"}, {"versioned_ensembl_gene_id":"ENSG00000160193.11","gene_symbol":"WDR4","gene_name":"WD repeat domain 4 [Source:HGNC Symbol;Acc:HGNC:12756]","synonyms":"TRMT82,TRM82","biotype":"protein_coding","ncbi_id":"10785","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]","start":42843094,"end":42879568,"strand":-1,"description":"WD repeat domain 4 [Source:HGNC Symbol;Acc:HGNC:12756]"}, {"versioned_ensembl_gene_id":"ENSG00000213903.8","gene_symbol":"LTB4R","gene_name":"leukotriene B4 receptor [Source:HGNC Symbol;Acc:HGNC:6713]","synonyms":"P2Y7,P2RY7,LTB4R1,GPR16,CMKRL1,BLTR","biotype":"protein_coding","ncbi_id":"1241","summary":null,"start":24311450,"end":24318036,"strand":1,"description":"leukotriene B4 receptor [Source:HGNC Symbol;Acc:HGNC:6713]"}, {"versioned_ensembl_gene_id":"ENSG00000184022.4","gene_symbol":"OR2T10","gene_name":"olfactory receptor family 2 subfamily T member 10 [Source:HGNC Symbol;Acc:HGNC:19573]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127069","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248590487,"end":248597700,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 10 [Source:HGNC Symbol;Acc:HGNC:19573]"}, {"versioned_ensembl_gene_id":"ENSG00000254771.1","gene_symbol":"AP001893.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126179497,"end":126179698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229594.1","gene_symbol":"AL159987.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55633031,"end":55635656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266959.1","gene_symbol":"AC005786.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3568120,"end":3568273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116478.11","gene_symbol":"HDAC1","gene_name":"histone deacetylase 1 [Source:HGNC Symbol;Acc:HGNC:4852]","synonyms":"RPD3L1,HD1,GON-10","biotype":"protein_coding","ncbi_id":"3065","summary":"Histone acetylation and deacetylation, catalyzed by multisubunit complexes, play a key role in the regulation of eukaryotic gene expression. The protein encoded by this gene belongs to the histone deacetylase/acuc/apha family and is a component of the histone deacetylase complex. It also interacts with retinoblastoma tumor-suppressor protein and this complex is a key element in the control of cell proliferation and differentiation. Together with metastasis-associated protein-2, it deacetylates p53 and modulates its effect on cell growth and apoptosis. [provided by RefSeq, Jul 2008]","start":32292086,"end":32333635,"strand":1,"description":"histone deacetylase 1 [Source:HGNC Symbol;Acc:HGNC:4852]"}, {"versioned_ensembl_gene_id":"ENSG00000128989.10","gene_symbol":"ARPP19","gene_name":"cAMP regulated phosphoprotein 19 [Source:HGNC Symbol;Acc:HGNC:16967]","synonyms":"ENSAL,ARPP16,ARPP-19,ARPP-16","biotype":"protein_coding","ncbi_id":"10776","summary":"The 19-kD cAMP-regulated phosphoprotein plays a role in regulating mitosis by inhibiting protein phosphatase-2A (PP2A; see MIM 176915) (summary by Gharbi-Ayachi et al., 2010 [PubMed 21164014]).[supplied by OMIM, Feb 2011]","start":52547045,"end":52569883,"strand":-1,"description":"cAMP regulated phosphoprotein 19 [Source:HGNC Symbol;Acc:HGNC:16967]"}, {"versioned_ensembl_gene_id":"ENSG00000243916.1","gene_symbol":"AC092183.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15439527,"end":15440401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224183.1","gene_symbol":"SDHDP6","gene_name":"succinate dehydrogenase complex subunit D pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:10689]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"29768","summary":null,"start":25294164,"end":25294643,"strand":-1,"description":"succinate dehydrogenase complex subunit D pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:10689]"}, {"versioned_ensembl_gene_id":"ENSG00000124785.8","gene_symbol":"NRN1","gene_name":"neuritin 1 [Source:HGNC Symbol;Acc:HGNC:17972]","synonyms":"NRN","biotype":"protein_coding","ncbi_id":"51299","summary":"This gene encodes a member of the neuritin family, and is expressed in postmitotic-differentiating neurons of the developmental nervous system and neuronal structures associated with plasticity in the adult. The expression of this gene can be induced by neural activity and neurotrophins. The encoded protein contains a consensus cleavage signal found in glycosylphoshatidylinositol (GPI)-anchored proteins. The encoded protein promotes neurite outgrowth and arborization, suggesting its role in promoting neuritogenesis. Overexpression of the encoded protein may be associated with astrocytoma progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":5997999,"end":6007605,"strand":-1,"description":"neuritin 1 [Source:HGNC Symbol;Acc:HGNC:17972]"}, {"versioned_ensembl_gene_id":"ENSG00000227666.1","gene_symbol":"CYCSP24","gene_name":"cytochrome c, somatic pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:24398]","synonyms":"HCP31,HCP24,HC3","biotype":"processed_pseudogene","ncbi_id":"360177","summary":null,"start":94038030,"end":94038345,"strand":1,"description":"cytochrome c, somatic pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:24398]"}, {"versioned_ensembl_gene_id":"ENSG00000253161.5","gene_symbol":"LINC01605","gene_name":"long intergenic non-protein coding RNA 1605 [Source:HGNC Symbol;Acc:HGNC:51654]","synonyms":"TCONS_00014973","biotype":"lincRNA","ncbi_id":"100507420","summary":null,"start":37421341,"end":37554183,"strand":-1,"description":"long intergenic non-protein coding RNA 1605 [Source:HGNC Symbol;Acc:HGNC:51654]"}, {"versioned_ensembl_gene_id":"ENSG00000181722.16","gene_symbol":"ZBTB20","gene_name":"zinc finger and BTB domain containing 20 [Source:HGNC Symbol;Acc:HGNC:13503]","synonyms":"ZNF288,ODA-8S,DPZF,DKFZp566F123","biotype":"protein_coding","ncbi_id":"26137","summary":"This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]","start":114314501,"end":115147271,"strand":-1,"description":"zinc finger and BTB domain containing 20 [Source:HGNC Symbol;Acc:HGNC:13503]"}, {"versioned_ensembl_gene_id":"ENSG00000261811.1","gene_symbol":"LINC02164","gene_name":"long intergenic non-protein coding RNA 2164 [Source:HGNC Symbol;Acc:HGNC:53025]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371066","summary":null,"start":5215394,"end":5220594,"strand":-1,"description":"long intergenic non-protein coding RNA 2164 [Source:HGNC Symbol;Acc:HGNC:53025]"}, {"versioned_ensembl_gene_id":"ENSG00000277570.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000272609.1","gene_symbol":"AC016252.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":138004649,"end":138005122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261146.1","gene_symbol":"AC007159.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137791973,"end":137796678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258711.2","gene_symbol":"AL358334.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50956259,"end":50962002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146469.12","gene_symbol":"VIP","gene_name":"vasoactive intestinal peptide [Source:HGNC Symbol;Acc:HGNC:12693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7432","summary":"The protein encoded by this gene belongs to the glucagon family. It stimulates myocardial contractility, causes vasodilation, increases glycogenolysis, lowers arterial blood pressure and relaxes the smooth muscle of trachea, stomach and gall bladder. The protein also acts as an antimicrobial peptide with antibacterial and antifungal activity. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Nov 2014]","start":152750798,"end":152759765,"strand":1,"description":"vasoactive intestinal peptide [Source:HGNC Symbol;Acc:HGNC:12693]"}, {"versioned_ensembl_gene_id":"ENSG00000226280.2","gene_symbol":"AL049641.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67373573,"end":67375520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226510.1","gene_symbol":"UPK1A-AS1","gene_name":"UPK1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40603]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100862728","summary":null,"start":35667948,"end":35673291,"strand":-1,"description":"UPK1A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40603]"}, {"versioned_ensembl_gene_id":"ENSG00000177174.1","gene_symbol":"OR14C36","gene_name":"olfactory receptor family 14 subfamily C member 36 [Source:HGNC Symbol;Acc:HGNC:15026]","synonyms":"OR5BF1","biotype":"protein_coding","ncbi_id":"127066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248348775,"end":248349713,"strand":1,"description":"olfactory receptor family 14 subfamily C member 36 [Source:HGNC Symbol;Acc:HGNC:15026]"}, {"versioned_ensembl_gene_id":"ENSG00000175215.10","gene_symbol":"CTDSP2","gene_name":"CTD small phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:17077]","synonyms":"OS4,SCP2,PSR2","biotype":"protein_coding","ncbi_id":"10106","summary":null,"start":57819927,"end":57846739,"strand":-1,"description":"CTD small phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:17077]"}, {"versioned_ensembl_gene_id":"ENSG00000115806.12","gene_symbol":"GORASP2","gene_name":"golgi reassembly stacking protein 2 [Source:HGNC Symbol;Acc:HGNC:17500]","synonyms":"GRS2,GRASP55,GOLPH6","biotype":"protein_coding","ncbi_id":"26003","summary":"This gene encodes a member of the Golgi reassembly stacking protein family. These proteins may play a role in the stacking of Golgi cisternae and Golgi ribbon formation, as well as Golgi fragmentation during apoptosis or mitosis. The encoded protein also plays a role in the intracellular transport of transforming growth factor alpha and may function as a molecular chaperone. A pseudogene of this gene is located on the short arm of chromosome 2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":170928464,"end":170967129,"strand":1,"description":"golgi reassembly stacking protein 2 [Source:HGNC Symbol;Acc:HGNC:17500]"}, {"versioned_ensembl_gene_id":"ENSG00000235892.1","gene_symbol":"PKMP2","gene_name":"pyruvate kinase, muscle pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44244]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402408","summary":null,"start":66497748,"end":66499424,"strand":1,"description":"pyruvate kinase, muscle pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44244]"}, {"versioned_ensembl_gene_id":"ENSG00000253336.1","gene_symbol":"AC018992.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123288355,"end":123290503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230295.1","gene_symbol":"GTF2IP23","gene_name":"general transcription factor IIi pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51735]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101929580","summary":null,"start":66880708,"end":66882981,"strand":1,"description":"general transcription factor IIi pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51735]"}, {"versioned_ensembl_gene_id":"ENSG00000282398.1","gene_symbol":"IGHV3-47","gene_name":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28425","summary":null,"start":106543263,"end":106543708,"strand":-1,"description":"immunoglobulin heavy variable 3-47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5605]"}, {"versioned_ensembl_gene_id":"ENSG00000219039.2","gene_symbol":"AC005102.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75835663,"end":75836141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231848.1","gene_symbol":"AC012354.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44996413,"end":44996873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162727.3","gene_symbol":"OR2M5","gene_name":"olfactory receptor family 2 subfamily M member 5 [Source:HGNC Symbol;Acc:HGNC:19576]","synonyms":"OR2M5P","biotype":"protein_coding","ncbi_id":"127059","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248145148,"end":248146086,"strand":1,"description":"olfactory receptor family 2 subfamily M member 5 [Source:HGNC Symbol;Acc:HGNC:19576]"}, {"versioned_ensembl_gene_id":"ENSG00000264334.1","gene_symbol":"AC134978.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77983020,"end":77986610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254599.1","gene_symbol":"AP003715.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98676391,"end":98683735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265174.1","gene_symbol":"AP005202.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6557822,"end":6558654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242748.1","gene_symbol":"RPL23AP81","gene_name":"ribosomal protein L23a pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:36246]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271627","summary":null,"start":41196691,"end":41197157,"strand":1,"description":"ribosomal protein L23a pseudogene 81 [Source:HGNC Symbol;Acc:HGNC:36246]"}, {"versioned_ensembl_gene_id":"ENSG00000224706.1","gene_symbol":"RPS17P13","gene_name":"ribosomal protein S17 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36664]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271073","summary":null,"start":37116779,"end":37117185,"strand":1,"description":"ribosomal protein S17 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36664]"}, {"versioned_ensembl_gene_id":"ENSG00000264164.1","gene_symbol":"AC090616.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32083179,"end":32097065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151881.14","gene_symbol":"TMEM267","gene_name":"transmembrane protein 267 [Source:HGNC Symbol;Acc:HGNC:26139]","synonyms":"FLJ21657,C5orf28","biotype":"protein_coding","ncbi_id":"64417","summary":null,"start":43444252,"end":43483893,"strand":-1,"description":"transmembrane protein 267 [Source:HGNC Symbol;Acc:HGNC:26139]"}, {"versioned_ensembl_gene_id":"ENSG00000226067.6","gene_symbol":"LINC00623","gene_name":"long intergenic non-protein coding RNA 623 [Source:HGNC Symbol;Acc:HGNC:44252]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728855","summary":null,"start":120913275,"end":121009291,"strand":1,"description":"long intergenic non-protein coding RNA 623 [Source:HGNC Symbol;Acc:HGNC:44252]"}, {"versioned_ensembl_gene_id":"ENSG00000161860.7","gene_symbol":"SYCE2","gene_name":"synaptonemal complex central element protein 2 [Source:HGNC Symbol;Acc:HGNC:27411]","synonyms":"CESC1","biotype":"protein_coding","ncbi_id":"256126","summary":"The protein encoded by this gene is part of the synaptonemal complex formed between homologous chromosomes during meiotic prophase. The encoded protein associates with SYCP1 and SYCE1 and is found only where chromosome cores are synapsed. [provided by RefSeq, Dec 2012]","start":12898786,"end":12919276,"strand":-1,"description":"synaptonemal complex central element protein 2 [Source:HGNC Symbol;Acc:HGNC:27411]"}, {"versioned_ensembl_gene_id":"ENSG00000269576.1","gene_symbol":"HNRNPMP2","gene_name":"heterogeneous nuclear ribonucleoprotein M pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48746]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390948","summary":null,"start":46809585,"end":46810183,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein M pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48746]"}, {"versioned_ensembl_gene_id":"ENSG00000204662.2","gene_symbol":"CST9LP1","gene_name":"cystatin 9-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39552]","synonyms":"CTES7C","biotype":"unprocessed_pseudogene","ncbi_id":"128820","summary":null,"start":23547764,"end":23550652,"strand":-1,"description":"cystatin 9-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39552]"}, {"versioned_ensembl_gene_id":"ENSG00000274649.1","gene_symbol":"AL512624.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19511244,"end":19511712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257395.1","gene_symbol":"AL512310.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19681420,"end":19684739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257846.2","gene_symbol":"AL512310.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19668829,"end":19670003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233360.4","gene_symbol":"Z83844.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37641832,"end":37658377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225793.2","gene_symbol":"AL080250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75285014,"end":75297003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214063.10","gene_symbol":"TSPAN4","gene_name":"tetraspanin 4 [Source:HGNC Symbol;Acc:HGNC:11859]","synonyms":"TSPAN-4,TM4SF7,TETRASPAN,NAG-2","biotype":"protein_coding","ncbi_id":"7106","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and is similar in sequence to its family member CD53 antigen. It is known to complex with integrins and other transmembrane 4 superfamily proteins. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":842808,"end":867116,"strand":1,"description":"tetraspanin 4 [Source:HGNC Symbol;Acc:HGNC:11859]"}, {"versioned_ensembl_gene_id":"ENSG00000213047.12","gene_symbol":"DENND1B","gene_name":"DENN domain containing 1B [Source:HGNC Symbol;Acc:HGNC:28404]","synonyms":"MGC27044,FLJ20054,FAM31B,C1orf218","biotype":"protein_coding","ncbi_id":"163486","summary":"Clathrin (see MIM 118955)-mediated endocytosis is a major mechanism for internalization of proteins and lipids. Members of the connecdenn family, such as DENND1B, function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2; see MIM 601024). Thus, connecdenns link RAB35 activation with the clathrin machinery (Marat and McPherson, 2010 [PubMed 20154091]).[supplied by OMIM, Nov 2010]","start":197504748,"end":197775696,"strand":-1,"description":"DENN domain containing 1B [Source:HGNC Symbol;Acc:HGNC:28404]"}, {"versioned_ensembl_gene_id":"ENSG00000108231.12","gene_symbol":"LGI1","gene_name":"leucine rich glioma inactivated 1 [Source:HGNC Symbol;Acc:HGNC:6572]","synonyms":"IB1099,ETL1,EPT,EPITEMPIN","biotype":"protein_coding","ncbi_id":"9211","summary":"This gene encodes a member of the secreted leucine-rich repeat (LRR) superfamily and shares homology with members of the SLIT protein family. The encoded protein may regulate the activity of voltage-gated potassium channels and may be involved in neuronal growth regulation and cell survival. This gene is rearranged as a result of translocations in glioblastoma cell lines, and it is frequently down-regulated or rearranged in malignant gliomas. Mutations in this gene result in autosomal dominant lateral temporal epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":93757809,"end":93806272,"strand":1,"description":"leucine rich glioma inactivated 1 [Source:HGNC Symbol;Acc:HGNC:6572]"}, {"versioned_ensembl_gene_id":"ENSG00000272432.1","gene_symbol":"AL031432.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25247837,"end":25248321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250778.1","gene_symbol":"AC004980.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76521611,"end":76522074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188850.9","gene_symbol":"AC114947.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":43336164,"end":43348716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267407.1","gene_symbol":"AC008794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31542039,"end":31554797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267636.1","gene_symbol":"AC008992.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31421997,"end":31427302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217139.2","gene_symbol":"AL603865.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121682925,"end":121684272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104763.18","gene_symbol":"ASAH1","gene_name":"N-acylsphingosine amidohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:735]","synonyms":"PHP32,FLJ21558,ASAH,ACDase,AC","biotype":"protein_coding","ncbi_id":"427","summary":"This gene encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. Processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid. This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in this gene are associated with the lysosomal storage disorder, Farber lipogranulomatosis, and a neuromuscular disorder, spinal muscular atrophy with progressive myoclonic epilepsy. [provided by RefSeq, Oct 2015]","start":18055992,"end":18084998,"strand":-1,"description":"N-acylsphingosine amidohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:735]"}, {"versioned_ensembl_gene_id":"ENSG00000104154.6","gene_symbol":"SLC30A4","gene_name":"solute carrier family 30 member 4 [Source:HGNC Symbol;Acc:HGNC:11015]","synonyms":"ZNT4","biotype":"protein_coding","ncbi_id":"7782","summary":"Zinc is the second most abundant trace metal in the human body. It is an essential element, serving both a structural role, as in the formation of zinc fingers in DNA-binding proteins, and a catalytic role in metalloenzymes, such as pancreatic carboxypeptidases (e.g., MIM 114852), alkaline phosphatases (e.g., MIM 171760), various dehydrogenases, and superoxide dismutases (e.g., MIM 147450). SLC30A4, or ZNT4, belongs to the ZNT family of zinc transporters. ZNTs are involved in transporting zinc out of the cytoplasm and have similar structures, consisting of 6 transmembrane domains and a histidine-rich cytoplasmic loop (Huang and Gitschier, 1997 [PubMed 9354792]).[supplied by OMIM, Mar 2008]","start":45479611,"end":45522807,"strand":-1,"description":"solute carrier family 30 member 4 [Source:HGNC Symbol;Acc:HGNC:11015]"}, {"versioned_ensembl_gene_id":"ENSG00000274394.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736497,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000226356.2","gene_symbol":"AC092850.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131292068,"end":131293176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127774.6","gene_symbol":"EMC6","gene_name":"ER membrane protein complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:28430]","synonyms":"TMEM93,MGC2963","biotype":"protein_coding","ncbi_id":"83460","summary":null,"start":3668815,"end":3669668,"strand":1,"description":"ER membrane protein complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:28430]"}, {"versioned_ensembl_gene_id":"ENSG00000182393.2","gene_symbol":"IFNL1","gene_name":"interferon lambda 1 [Source:HGNC Symbol;Acc:HGNC:18363]","synonyms":"IL-29,IL29","biotype":"protein_coding","ncbi_id":"282618","summary":"This gene encodes a cytokine distantly related to type I interferons and the IL-10 family. This gene, interleukin 28A (IL28A), and interleukin 28B (IL28B) are three closely related cytokine genes that form a cytokine gene cluster on a chromosomal region mapped to 19q13. Expression of the cytokines encoded by the three genes can be induced by viral infection. All three cytokines have been shown to interact with a heterodimeric class II cytokine receptor that consists of interleukin 10 receptor, beta (IL10RB) and interleukin 28 receptor, alpha (IL28RA). [provided by RefSeq, Jul 2008]","start":39296325,"end":39298673,"strand":1,"description":"interferon lambda 1 [Source:HGNC Symbol;Acc:HGNC:18363]"}, {"versioned_ensembl_gene_id":"ENSG00000131831.17","gene_symbol":"RAI2","gene_name":"retinoic acid induced 2 [Source:HGNC Symbol;Acc:HGNC:9835]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10742","summary":"Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":17800049,"end":17861337,"strand":-1,"description":"retinoic acid induced 2 [Source:HGNC Symbol;Acc:HGNC:9835]"}, {"versioned_ensembl_gene_id":"ENSG00000185823.3","gene_symbol":"NPAP1","gene_name":"nuclear pore associated protein 1 [Source:HGNC Symbol;Acc:HGNC:1190]","synonyms":"C15orf2","biotype":"protein_coding","ncbi_id":"23742","summary":"This intronless retrogene is located in the Prader-Willi syndrome region on chromosome 15. This gene exhibits tissue-specific imprinting. Expression in adult testis and brain is biallelic, while expression in fetal brain is monoallelic and only from the paternal chromosome. The encoded protein is associated with the nuclear pore complex. [provided by RefSeq, Mar 2021]","start":24675868,"end":24683393,"strand":1,"description":"nuclear pore associated protein 1 [Source:HGNC Symbol;Acc:HGNC:1190]"}, {"versioned_ensembl_gene_id":"ENSG00000270382.1","gene_symbol":"AL109918.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52657373,"end":52657651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227197.1","gene_symbol":"AC009365.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132830693,"end":132849593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248625.1","gene_symbol":"AC079768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169832653,"end":169833363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282702.1","gene_symbol":"AC245166.2","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106331887,"end":106332323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229693.2","gene_symbol":"AL606530.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96620654,"end":96621903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092853.13","gene_symbol":"CLSPN","gene_name":"claspin [Source:HGNC Symbol;Acc:HGNC:19715]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63967","summary":"The product of this gene is an essential upstream regulator of checkpoint kinase 1 and triggers a checkpoint arrest of the cell cycle in response to replicative stress or DNA damage. The protein is also required for efficient DNA replication during a normal S phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":35720218,"end":35769967,"strand":-1,"description":"claspin [Source:HGNC Symbol;Acc:HGNC:19715]"}, {"versioned_ensembl_gene_id":"ENSG00000225939.1","gene_symbol":"AL662833.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31298844,"end":31299578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270822.1","gene_symbol":"AC092032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5009164,"end":5009328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233486.3","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"D84394.7,USP8P,KIAA0055-hom","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31266612,"end":31269783,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000189337.16","gene_symbol":"KAZN","gene_name":"kazrin, periplakin interacting protein [Source:HGNC Symbol;Acc:HGNC:29173]","synonyms":"KIAA1026,KAZRIN,FLJ43806","biotype":"protein_coding","ncbi_id":"23254","summary":"This gene encodes a protein that plays a role in desmosome assembly, cell adhesion, cytoskeletal organization, and epidermal differentiation. This protein co-localizes with desmoplakin and the cytolinker protein periplakin. In general, this protein localizes to the nucleus, desmosomes, cell membrane, and cortical actin-based structures. Some isoforms of this protein also associate with microtubules. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity has not been verified. [provided by RefSeq, Aug 2011]","start":13892792,"end":15118043,"strand":1,"description":"kazrin, periplakin interacting protein [Source:HGNC Symbol;Acc:HGNC:29173]"}, {"versioned_ensembl_gene_id":"ENSG00000278514.1","gene_symbol":"AC068831.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91022766,"end":91023200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236817.5","gene_symbol":"AL606804.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":247565639,"end":247640854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272711.1","gene_symbol":"AC019069.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74832655,"end":74833987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115946.7","gene_symbol":"PNO1","gene_name":"partner of NOB1 homolog [Source:HGNC Symbol;Acc:HGNC:32790]","synonyms":"RRP20,KHRBP1","biotype":"protein_coding","ncbi_id":"56902","summary":null,"start":68157844,"end":68176238,"strand":1,"description":"partner of NOB1 homolog [Source:HGNC Symbol;Acc:HGNC:32790]"}, {"versioned_ensembl_gene_id":"ENSG00000273064.1","gene_symbol":"AC017083.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68252870,"end":68253848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269986.1","gene_symbol":"AC040174.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":63066526,"end":63066990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231589.1","gene_symbol":"AC009110.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62596372,"end":62598449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235749.2","gene_symbol":"AL390860.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":247639749,"end":247747062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112304.10","gene_symbol":"ACOT13","gene_name":"acyl-CoA thioesterase 13 [Source:HGNC Symbol;Acc:HGNC:20999]","synonyms":"THEM2,HT012","biotype":"protein_coding","ncbi_id":"55856","summary":"This gene encodes a member of the thioesterase superfamily. In humans, the protein co-localizes with microtubules and is essential for sustained cell proliferation. The orthologous mouse protein forms a homotetramer and is associated with mitochondria. The mouse protein functions as a medium- and long-chain acyl-CoA thioesterase. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2009]","start":24667035,"end":24705065,"strand":1,"description":"acyl-CoA thioesterase 13 [Source:HGNC Symbol;Acc:HGNC:20999]"}, {"versioned_ensembl_gene_id":"ENSG00000248641.1","gene_symbol":"HMGA1P2","gene_name":"high mobility group AT-hook 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13322]","synonyms":"HMGIYL2,HMGA1L2","biotype":"processed_pseudogene","ncbi_id":"171559","summary":null,"start":73098822,"end":73099145,"strand":1,"description":"high mobility group AT-hook 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13322]"}, {"versioned_ensembl_gene_id":"ENSG00000218819.4","gene_symbol":"TDRD15","gene_name":"tudor domain containing 15 [Source:HGNC Symbol;Acc:HGNC:45037]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129278","summary":null,"start":21123917,"end":21143272,"strand":1,"description":"tudor domain containing 15 [Source:HGNC Symbol;Acc:HGNC:45037]"}, {"versioned_ensembl_gene_id":"ENSG00000177489.1","gene_symbol":"OR2G2","gene_name":"olfactory receptor family 2 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15007]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81470","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247588360,"end":247589313,"strand":1,"description":"olfactory receptor family 2 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:15007]"}, {"versioned_ensembl_gene_id":"ENSG00000257730.1","gene_symbol":"LSM6P2","gene_name":"LSM6 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462857","summary":null,"start":49770960,"end":49771136,"strand":1,"description":"LSM6 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37811]"}, {"versioned_ensembl_gene_id":"ENSG00000260756.1","gene_symbol":"AC131649.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10351440,"end":10352752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100714.15","gene_symbol":"MTHFD1","gene_name":"methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:7432]","synonyms":"MTHFD,MTHFC","biotype":"protein_coding","ncbi_id":"4522","summary":"This gene encodes a protein that possesses three distinct enzymatic activities, 5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methenyltetrahydrofolate cyclohydrolase and 10-formyltetrahydrofolate synthetase. Each of these activities catalyzes one of three sequential reactions in the interconversion of 1-carbon derivatives of tetrahydrofolate, which are substrates for methionine, thymidylate, and de novo purine syntheses. The trifunctional enzymatic activities are conferred by two major domains, an aminoterminal portion containing the dehydrogenase and cyclohydrolase activities and a larger synthetase domain. [provided by RefSeq, Jul 2008]","start":64388031,"end":64463457,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:7432]"}, {"versioned_ensembl_gene_id":"ENSG00000280891.1","gene_symbol":"AL606534.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":243005845,"end":243007468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160957.12","gene_symbol":"RECQL4","gene_name":"RecQ like helicase 4 [Source:HGNC Symbol;Acc:HGNC:9949]","synonyms":"RecQ4","biotype":"protein_coding","ncbi_id":"9401","summary":"The protein encoded by this gene is a DNA helicase that belongs to the RecQ helicase family. DNA helicases unwind double-stranded DNA into single-stranded DNAs and may modulate chromosome segregation. This gene is predominantly expressed in thymus and testis. Mutations in this gene are associated with Rothmund-Thomson, RAPADILINO and Baller-Gerold syndromes. [provided by RefSeq, Jan 2010]","start":144511288,"end":144517845,"strand":-1,"description":"RecQ like helicase 4 [Source:HGNC Symbol;Acc:HGNC:9949]"}, {"versioned_ensembl_gene_id":"ENSG00000229853.1","gene_symbol":"AL034418.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47630266,"end":47631438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279812.1","gene_symbol":"AC120057.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7192295,"end":7192448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234529.2","gene_symbol":"GAPDHP19","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:23947]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"140028","summary":null,"start":19327569,"end":19328573,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:23947]"}, {"versioned_ensembl_gene_id":"ENSG00000130167.13","gene_symbol":"TSPAN16","gene_name":"tetraspanin 16 [Source:HGNC Symbol;Acc:HGNC:30725]","synonyms":"TM4SF16,TM4-B,TM-8","biotype":"protein_coding","ncbi_id":"26526","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein might couple to signal transduction pathways and possibly modulate cellular activation and adhesion in haemopoietic and neural tissue. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":11296139,"end":11326996,"strand":1,"description":"tetraspanin 16 [Source:HGNC Symbol;Acc:HGNC:30725]"}, {"versioned_ensembl_gene_id":"ENSG00000279885.1","gene_symbol":"AP005060.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6394847,"end":6398020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275717.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816473,"end":54830785,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000279330.1","gene_symbol":"AJ003147.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3273609,"end":3275807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131669.9","gene_symbol":"NINJ1","gene_name":"ninjurin 1 [Source:HGNC Symbol;Acc:HGNC:7824]","synonyms":"NIN1","biotype":"protein_coding","ncbi_id":"4814","summary":"The ninjurin protein is upregulated after nerve injury both in dorsal root ganglion neurons and in Schwann cells (Araki and Milbrandt, 1996 [PubMed 8780658]). It demonstrates properties of a homophilic adhesion molecule and promotes neurite outgrowth from primary cultured dorsal root ganglion neurons.[supplied by OMIM, Aug 2009]","start":93121489,"end":93134288,"strand":-1,"description":"ninjurin 1 [Source:HGNC Symbol;Acc:HGNC:7824]"}, {"versioned_ensembl_gene_id":"ENSG00000232448.1","gene_symbol":"AL354824.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10180235,"end":10185775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230506.1","gene_symbol":"AL354824.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10173520,"end":10196990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231894.2","gene_symbol":"WDR95P","gene_name":"WD repeat domain 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:42637]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100873795","summary":null,"start":31063306,"end":31115699,"strand":1,"description":"WD repeat domain 95, pseudogene [Source:HGNC Symbol;Acc:HGNC:42637]"}, {"versioned_ensembl_gene_id":"ENSG00000113924.11","gene_symbol":"HGD","gene_name":"homogentisate 1,2-dioxygenase [Source:HGNC Symbol;Acc:HGNC:4892]","synonyms":"HGO,AKU","biotype":"protein_coding","ncbi_id":"3081","summary":"This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]","start":120628173,"end":120682571,"strand":-1,"description":"homogentisate 1,2-dioxygenase [Source:HGNC Symbol;Acc:HGNC:4892]"}, {"versioned_ensembl_gene_id":"ENSG00000132623.15","gene_symbol":"ANKEF1","gene_name":"ankyrin repeat and EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15803]","synonyms":"FLJ21669,dJ839B4.6,ANKRD5","biotype":"protein_coding","ncbi_id":"63926","summary":null,"start":9986126,"end":10058303,"strand":1,"description":"ankyrin repeat and EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15803]"}, {"versioned_ensembl_gene_id":"ENSG00000259972.2","gene_symbol":"AC009120.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":74305127,"end":74335346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279031.1","gene_symbol":"AC004232.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3292879,"end":3293403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255076.2","gene_symbol":"AC084838.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":14879057,"end":14879819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260884.1","gene_symbol":"AC009120.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74313337,"end":74315634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214366.4","gene_symbol":"EIF4EP5","gene_name":"eukaryotic translation initiation factor 4E pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51463]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131565","summary":null,"start":14309033,"end":14309672,"strand":1,"description":"eukaryotic translation initiation factor 4E pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51463]"}, {"versioned_ensembl_gene_id":"ENSG00000239763.2","gene_symbol":"AC009120.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74312609,"end":74313390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258728.1","gene_symbol":"AL162231.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34646645,"end":34657113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179455.7","gene_symbol":"MKRN3","gene_name":"makorin ring finger protein 3 [Source:HGNC Symbol;Acc:HGNC:7114]","synonyms":"MGC88288,D15S9,ZNF127,ZFP127,RNF63","biotype":"protein_coding","ncbi_id":"7681","summary":"The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008]","start":23565678,"end":23630075,"strand":1,"description":"makorin ring finger protein 3 [Source:HGNC Symbol;Acc:HGNC:7114]"}, {"versioned_ensembl_gene_id":"ENSG00000223865.10","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33075926,"end":33087201,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000178605.13","gene_symbol":"GTPBP6","gene_name":"GTP binding protein 6 (putative) [Source:HGNC Symbol;Acc:HGNC:30189]","synonyms":"PGPL,FLJ20977","biotype":"protein_coding","ncbi_id":"8225","summary":"This gene encodes a GTP binding protein and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. [provided by RefSeq, Nov 2011]","start":304529,"end":318819,"strand":-1,"description":"GTP binding protein 6 (putative) [Source:HGNC Symbol;Acc:HGNC:30189]"}, {"versioned_ensembl_gene_id":"ENSG00000254575.1","gene_symbol":"AC022039.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14161297,"end":14165359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261079.1","gene_symbol":"AC009053.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74367462,"end":74369826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214331.8","gene_symbol":"AC009053.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":74332402,"end":74368240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226474.1","gene_symbol":"AP000532.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15615402,"end":15615578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213927.3","gene_symbol":"CCL27","gene_name":"C-C motif chemokine ligand 27 [Source:HGNC Symbol;Acc:HGNC:10626]","synonyms":"SCYA27,PESKY,ILC,ESkine,CTAK,CTACK,ALP,skinkine","biotype":"protein_coding","ncbi_id":"10850","summary":"This gene is one of several CC cytokine genes clustered on the p-arm of chromosome 9. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The protein encoded by this gene is chemotactic for skin-associated memory T lymphocytes. This cytokine may also play a role in mediating homing of lymphocytes to cutaneous sites. It specifically binds to chemokine receptor 10 (CCR10). Studies of a similar murine protein indicate that these protein-receptor interactions have a pivotal role in T cell-mediated skin inflammation. [provided by RefSeq, Sep 2014]","start":34661880,"end":34664048,"strand":-1,"description":"C-C motif chemokine ligand 27 [Source:HGNC Symbol;Acc:HGNC:10626]"}, {"versioned_ensembl_gene_id":"ENSG00000282840.1","gene_symbol":"AC004554.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11668401,"end":11757718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223418.1","gene_symbol":"AC004554.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11704123,"end":11705590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261632.1","gene_symbol":"AC022872.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71972206,"end":72040265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260173.1","gene_symbol":"AC020779.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72140504,"end":72155459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235156.5","gene_symbol":"TMEM30CP","gene_name":"transmembrane protein 30C, pseudogene [Source:HGNC Symbol;Acc:HGNC:30443]","synonyms":"TMEM30C,CDC50C","biotype":"transcribed_unitary_pseudogene","ncbi_id":"644444","summary":null,"start":100185687,"end":100211766,"strand":1,"description":"transmembrane protein 30C, pseudogene [Source:HGNC Symbol;Acc:HGNC:30443]"}, {"versioned_ensembl_gene_id":"ENSG00000232878.3","gene_symbol":"DPYD-AS1","gene_name":"DPYD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40195]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873932","summary":null,"start":97095923,"end":97322955,"strand":1,"description":"DPYD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40195]"}, {"versioned_ensembl_gene_id":"ENSG00000262375.1","gene_symbol":"AL157402.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198609211,"end":198610355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260037.5","gene_symbol":"AC104938.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71818396,"end":71823384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204279.7","gene_symbol":"PAGE3","gene_name":"PAGE family member 3 [Source:HGNC Symbol;Acc:HGNC:4110]","synonyms":"CT16.6,PAGE-3,GAGED1","biotype":"protein_coding","ncbi_id":"139793","summary":"This gene is a member of family of proteins that are expressed in a variety of tumors and in some fetal and reproductive tissues. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2015]","start":55258412,"end":55264846,"strand":-1,"description":"PAGE family member 3 [Source:HGNC Symbol;Acc:HGNC:4110]"}, {"versioned_ensembl_gene_id":"ENSG00000226128.1","gene_symbol":"RPL26P9","gene_name":"ribosomal protein L26 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36180]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270885","summary":null,"start":97585862,"end":97586294,"strand":1,"description":"ribosomal protein L26 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36180]"}, {"versioned_ensembl_gene_id":"ENSG00000261215.1","gene_symbol":"AL162231.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":34661903,"end":34666029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224435.2","gene_symbol":"NF1P6","gene_name":"neurofibromin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:7771]","synonyms":"NF1L6,Em:AP000532.C22.1","biotype":"unprocessed_pseudogene","ncbi_id":"644637","summary":null,"start":15622601,"end":15632051,"strand":-1,"description":"neurofibromin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:7771]"}, {"versioned_ensembl_gene_id":"ENSG00000270911.1","gene_symbol":"AC114878.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97855575,"end":97856825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179902.12","gene_symbol":"C1orf194","gene_name":"chromosome 1 open reading frame 194 [Source:HGNC Symbol;Acc:HGNC:32331]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127003","summary":null,"start":109105951,"end":109113857,"strand":-1,"description":"chromosome 1 open reading frame 194 [Source:HGNC Symbol;Acc:HGNC:32331]"}, {"versioned_ensembl_gene_id":"ENSG00000230074.1","gene_symbol":"AL162231.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34665665,"end":34681298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230718.1","gene_symbol":"AC114878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97774669,"end":97775026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243568.2","gene_symbol":"AC020779.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72134641,"end":72135436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235777.1","gene_symbol":"DPYD-AS2","gene_name":"DPYD antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40196]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873933","summary":null,"start":97796921,"end":97798066,"strand":1,"description":"DPYD antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40196]"}, {"versioned_ensembl_gene_id":"ENSG00000274830.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738514,"end":54753065,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000278833.4","gene_symbol":"GU182360.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":54786437,"end":54798259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260978.1","gene_symbol":"AC126407.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23567264,"end":23569657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228193.1","gene_symbol":"ELOCP14","gene_name":"elongin C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38150]","synonyms":"TCEB1P14","biotype":"processed_pseudogene","ncbi_id":"100462876","summary":null,"start":18787750,"end":18788080,"strand":1,"description":"elongin C pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38150]"}, {"versioned_ensembl_gene_id":"ENSG00000233684.2","gene_symbol":"LINC01865","gene_name":"long intergenic non-protein coding RNA 1865 [Source:HGNC Symbol;Acc:HGNC:52684]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373350","summary":null,"start":317912,"end":342118,"strand":1,"description":"long intergenic non-protein coding RNA 1865 [Source:HGNC Symbol;Acc:HGNC:52684]"}, {"versioned_ensembl_gene_id":"ENSG00000137070.17","gene_symbol":"IL11RA","gene_name":"interleukin 11 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5967]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3590","summary":"Interleukin 11 is a stromal cell-derived cytokine that belongs to a family of pleiotropic and redundant cytokines that use the gp130 transducing subunit in their high affinity receptors. This gene encodes the IL-11 receptor, which is a member of the hematopoietic cytokine receptor family. This particular receptor is very similar to ciliary neurotrophic factor, since both contain an extracellular region with a 2-domain structure composed of an immunoglobulin-like domain and a cytokine receptor-like domain. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]","start":34650702,"end":34661892,"strand":1,"description":"interleukin 11 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5967]"}, {"versioned_ensembl_gene_id":"ENSG00000260576.1","gene_symbol":"EIF5A2P1","gene_name":"eukaryotic translation initiation factor 5A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51467]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506058","summary":null,"start":72041194,"end":72041653,"strand":-1,"description":"eukaryotic translation initiation factor 5A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51467]"}, {"versioned_ensembl_gene_id":"ENSG00000228057.1","gene_symbol":"SEC63P1","gene_name":"SEC63 homolog, protein translocation regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41953]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420341","summary":null,"start":97545701,"end":97546958,"strand":1,"description":"SEC63 homolog, protein translocation regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41953]"}, {"versioned_ensembl_gene_id":"ENSG00000073417.14","gene_symbol":"PDE8A","gene_name":"phosphodiesterase 8A [Source:HGNC Symbol;Acc:HGNC:8793]","synonyms":"HsT19550","biotype":"protein_coding","ncbi_id":"5151","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE8 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]","start":84980440,"end":85139145,"strand":1,"description":"phosphodiesterase 8A [Source:HGNC Symbol;Acc:HGNC:8793]"}, {"versioned_ensembl_gene_id":"ENSG00000188641.12","gene_symbol":"DPYD","gene_name":"dihydropyrimidine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3012]","synonyms":"DPD","biotype":"protein_coding","ncbi_id":"1806","summary":"The protein encoded by this gene is a pyrimidine catabolic enzyme and the initial and rate-limiting factor in the pathway of uracil and thymidine catabolism. Mutations in this gene result in dihydropyrimidine dehydrogenase deficiency, an error in pyrimidine metabolism associated with thymine-uraciluria and an increased risk of toxicity in cancer patients receiving 5-fluorouracil chemotherapy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":97077743,"end":97921049,"strand":-1,"description":"dihydropyrimidine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3012]"}, {"versioned_ensembl_gene_id":"ENSG00000183760.10","gene_symbol":"ACP7","gene_name":"acid phosphatase 7, tartrate resistant (putative) [Source:HGNC Symbol;Acc:HGNC:33781]","synonyms":"PAPL1,PAPL,FLJ16165","biotype":"protein_coding","ncbi_id":"390928","summary":"Purple acid phosphatases (PAPs), including PAPL, are a family of binuclear metallohydrolases that have been identified in plants, animals, and fungi (Flanagan et al., 2006 [PubMed 16793224]).[supplied by OMIM, Mar 2008]","start":39083913,"end":39111493,"strand":1,"description":"acid phosphatase 7, tartrate resistant (putative) [Source:HGNC Symbol;Acc:HGNC:33781]"}, {"versioned_ensembl_gene_id":"ENSG00000180611.6","gene_symbol":"MB21D2","gene_name":"Mab-21 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30438]","synonyms":"C3orf59","biotype":"protein_coding","ncbi_id":"151963","summary":null,"start":192796815,"end":192918161,"strand":-1,"description":"Mab-21 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30438]"}, {"versioned_ensembl_gene_id":"ENSG00000066933.15","gene_symbol":"MYO9A","gene_name":"myosin IXA [Source:HGNC Symbol;Acc:HGNC:7608]","synonyms":"FLJ11061,MGC71859,FLJ13244","biotype":"protein_coding","ncbi_id":"4649","summary":"This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with Bardet-Biedl Syndrome. [provided by RefSeq, Dec 2011]","start":71822289,"end":72118577,"strand":-1,"description":"myosin IXA [Source:HGNC Symbol;Acc:HGNC:7608]"}, {"versioned_ensembl_gene_id":"ENSG00000182378.13","gene_symbol":"PLCXD1","gene_name":"phosphatidylinositol specific phospholipase C X domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23148]","synonyms":"FLJ11323","biotype":"protein_coding","ncbi_id":"55344","summary":"This gene is the most terminal protein-coding gene in the pseudoautosomal (PAR) region on chromosomes X and Y. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":276322,"end":303356,"strand":1,"description":"phosphatidylinositol specific phospholipase C X domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23148]"}, {"versioned_ensembl_gene_id":"ENSG00000253999.1","gene_symbol":"IGKV3D-31","gene_name":"immunoglobulin kappa variable 3D-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5827]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28872","summary":null,"start":89929701,"end":89930202,"strand":1,"description":"immunoglobulin kappa variable 3D-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5827]"}, {"versioned_ensembl_gene_id":"ENSG00000236436.1","gene_symbol":"AC012361.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20859771,"end":20861661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250500.1","gene_symbol":"AC017007.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112797050,"end":112798691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275353.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832684,"end":54848599,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000046774.9","gene_symbol":"MAGEC2","gene_name":"MAGE family member C2 [Source:HGNC Symbol;Acc:HGNC:13574]","synonyms":"MAGEE1,MAGE-C2,HCA587,CT10","biotype":"protein_coding","ncbi_id":"51438","summary":"This gene is a member of the MAGEC gene family. It is not expressed in normal tissues, except for testis, and is expressed in tumors of various histological types. This gene and the other MAGEC genes are clustered on chromosome Xq26-q27. [provided by RefSeq, Oct 2009]","start":142202345,"end":142205290,"strand":-1,"description":"MAGE family member C2 [Source:HGNC Symbol;Acc:HGNC:13574]"}, {"versioned_ensembl_gene_id":"ENSG00000270392.2","gene_symbol":"PFN1P2","gene_name":"profilin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24298]","synonyms":"COAS3,C1orf152","biotype":"transcribed_processed_pseudogene","ncbi_id":"767846","summary":null,"start":120432204,"end":120434052,"strand":-1,"description":"profilin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24298]"}, {"versioned_ensembl_gene_id":"ENSG00000279420.1","gene_symbol":"AC138627.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74053365,"end":74053965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262848.1","gene_symbol":"AC136624.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16290135,"end":16292242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263990.1","gene_symbol":"AC004253.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31873926,"end":31886666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284572.1","gene_symbol":"AC099654.15","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57196056,"end":57196564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256709.2","gene_symbol":"AL133271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106327534,"end":106327824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112695.11","gene_symbol":"COX7A2","gene_name":"cytochrome c oxidase subunit 7A2 [Source:HGNC Symbol;Acc:HGNC:2288]","synonyms":"COX7AL,COXVIIa-L","biotype":"protein_coding","ncbi_id":"1347","summary":"Cytochrome c oxidase, the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of three catalytic subunits encoded by mitochondrial genes, and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, while the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 2 (liver isoform) of subunit VIIa, with this polypeptide being present in both muscle and non-muscle tissues. In addition to polypeptide 2, subunit VIIa includes polypeptide 1 (muscle isoform), which is present only in muscle tissues, and a related protein, which is present in all tissues. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4 and 14. [provided by RefSeq, Oct 2009]","start":75237675,"end":75250323,"strand":-1,"description":"cytochrome c oxidase subunit 7A2 [Source:HGNC Symbol;Acc:HGNC:2288]"}, {"versioned_ensembl_gene_id":"ENSG00000221866.9","gene_symbol":"PLXNA4","gene_name":"plexin A4 [Source:HGNC Symbol;Acc:HGNC:9102]","synonyms":"FAYV2820,DKFZp434G0625PRO34003,PLXNA4B,PLXNA4A,KIAA1550","biotype":"protein_coding","ncbi_id":"91584","summary":null,"start":132123332,"end":132648688,"strand":-1,"description":"plexin A4 [Source:HGNC Symbol;Acc:HGNC:9102]"}, {"versioned_ensembl_gene_id":"ENSG00000248633.1","gene_symbol":"WRBP1","gene_name":"tryptophan rich basic protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44010]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"256085","summary":null,"start":112693459,"end":112693792,"strand":-1,"description":"tryptophan rich basic protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44010]"}, {"versioned_ensembl_gene_id":"ENSG00000213935.3","gene_symbol":"AC092610.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4865432,"end":4865804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239975.2","gene_symbol":"IGKV1D-33","gene_name":"immunoglobulin kappa variable 1D-33 [Source:HGNC Symbol;Acc:HGNC:5753]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28896","summary":null,"start":89913982,"end":89916052,"strand":1,"description":"immunoglobulin kappa variable 1D-33 [Source:HGNC Symbol;Acc:HGNC:5753]"}, {"versioned_ensembl_gene_id":"ENSG00000218823.1","gene_symbol":"PAPOLB","gene_name":"poly(A) polymerase beta [Source:HGNC Symbol;Acc:HGNC:15970]","synonyms":"PAPT","biotype":"protein_coding","ncbi_id":"56903","summary":null,"start":4857733,"end":4861994,"strand":-1,"description":"poly(A) polymerase beta [Source:HGNC Symbol;Acc:HGNC:15970]"}, {"versioned_ensembl_gene_id":"ENSG00000232578.4","gene_symbol":"AC093311.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94592771,"end":94594791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251340.1","gene_symbol":"MTCYBP35","gene_name":"mitochondrially encoded cytochrome b pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52303]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729150","summary":null,"start":94569540,"end":94570676,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52303]"}, {"versioned_ensembl_gene_id":"ENSG00000072778.19","gene_symbol":"ACADVL","gene_name":"acyl-CoA dehydrogenase, very long chain [Source:HGNC Symbol;Acc:HGNC:92]","synonyms":"LCACD,ACAD6,VLCAD","biotype":"protein_coding","ncbi_id":"37","summary":"The protein encoded by this gene is targeted to the inner mitochondrial membrane where it catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. This acyl-Coenzyme A dehydrogenase is specific to long-chain and very-long-chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta-oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":7217125,"end":7225273,"strand":1,"description":"acyl-CoA dehydrogenase, very long chain [Source:HGNC Symbol;Acc:HGNC:92]"}, {"versioned_ensembl_gene_id":"ENSG00000100360.14","gene_symbol":"IFT27","gene_name":"intraflagellar transport 27 [Source:HGNC Symbol;Acc:HGNC:18626]","synonyms":"RAYL,RABL4,BBS19","biotype":"protein_coding","ncbi_id":"11020","summary":"This gene encodes a GTP-binding protein that is a core component of the intraflagellar transport complex B. Characterization of the similar Chlamydomonas protein indicates a function in cell cycle control. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":36758202,"end":36776256,"strand":-1,"description":"intraflagellar transport 27 [Source:HGNC Symbol;Acc:HGNC:18626]"}, {"versioned_ensembl_gene_id":"ENSG00000272894.5","gene_symbol":"AC004982.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7552462,"end":7566996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267726.1","gene_symbol":"LINC02565","gene_name":"long intergenic non-protein coding RNA 2565 [Source:HGNC Symbol;Acc:HGNC:53605]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57169615,"end":57171194,"strand":-1,"description":"long intergenic non-protein coding RNA 2565 [Source:HGNC Symbol;Acc:HGNC:53605]"}, {"versioned_ensembl_gene_id":"ENSG00000213620.3","gene_symbol":"AL121657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31290762,"end":31291604,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233782.1","gene_symbol":"ZNF90P3","gene_name":"zinc finger protein 90 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39882]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873799","summary":null,"start":63087070,"end":63088261,"strand":-1,"description":"zinc finger protein 90 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39882]"}, {"versioned_ensembl_gene_id":"ENSG00000227148.1","gene_symbol":"AC069285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63044827,"end":63054431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249242.7","gene_symbol":"TMEM150C","gene_name":"transmembrane protein 150C [Source:HGNC Symbol;Acc:HGNC:37263]","synonyms":"TTN3,FLJ12993","biotype":"protein_coding","ncbi_id":"441027","summary":"This gene encodes a transmembrane protein component of a mechanosensitve ion channel that is activated by mechanical stimuli in various cell types and confers slowly adapting, mechanically activated currents in dorsal root ganglion neurons. Mechanically activated ion channels are sensors that are critical for hearing, touch, pain, and blood pressure regulation. [provided by RefSeq, Jul 2017]","start":82483170,"end":82562357,"strand":-1,"description":"transmembrane protein 150C [Source:HGNC Symbol;Acc:HGNC:37263]"}, {"versioned_ensembl_gene_id":"ENSG00000233918.1","gene_symbol":"AC128676.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62275361,"end":62275678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223591.5","gene_symbol":"CENPVL1","gene_name":"centromere protein V like 1 [Source:HGNC Symbol;Acc:HGNC:31851]","synonyms":"PRR6L1,CENPVP1","biotype":"protein_coding","ncbi_id":"389857","summary":null,"start":51710512,"end":51712131,"strand":1,"description":"centromere protein V like 1 [Source:HGNC Symbol;Acc:HGNC:31851]"}, {"versioned_ensembl_gene_id":"ENSG00000275418.1","gene_symbol":"AC104971.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58659858,"end":58660524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160796.16","gene_symbol":"NBEAL2","gene_name":"neurobeachin like 2 [Source:HGNC Symbol;Acc:HGNC:31928]","synonyms":"KIAA0540","biotype":"protein_coding","ncbi_id":"23218","summary":"The protein encoded by this gene contains a beige and Chediak-Higashi (BEACH) domain and multiple WD40 domains, and may play a role in megakaryocyte alpha-granule biogenesis. Mutations in this gene are a cause of gray platelet syndrome. [provided by RefSeq, Dec 2011]","start":46979683,"end":47009703,"strand":1,"description":"neurobeachin like 2 [Source:HGNC Symbol;Acc:HGNC:31928]"}, {"versioned_ensembl_gene_id":"ENSG00000236238.2","gene_symbol":"AC093106.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131665507,"end":131665858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213261.3","gene_symbol":"EEF1B2P6","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51453]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647030","summary":null,"start":131661952,"end":131662624,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51453]"}, {"versioned_ensembl_gene_id":"ENSG00000214992.6","gene_symbol":"AKAP17BP","gene_name":"A-kinase anchoring protein 17B, pseudogene [Source:HGNC Symbol;Acc:HGNC:38514]","synonyms":"AKAP16BP,AKAP16B","biotype":"unprocessed_pseudogene","ncbi_id":"139516","summary":null,"start":119249346,"end":119257667,"strand":-1,"description":"A-kinase anchoring protein 17B, pseudogene [Source:HGNC Symbol;Acc:HGNC:38514]"}, {"versioned_ensembl_gene_id":"ENSG00000184068.2","gene_symbol":"AL021453.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41831215,"end":41834665,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236544.1","gene_symbol":"AC008060.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155421206,"end":155457099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196455.7","gene_symbol":"PIK3R4","gene_name":"phosphoinositide-3-kinase regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:8982]","synonyms":"p150,VPS15","biotype":"protein_coding","ncbi_id":"30849","summary":null,"start":130678935,"end":130746829,"strand":-1,"description":"phosphoinositide-3-kinase regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:8982]"}, {"versioned_ensembl_gene_id":"ENSG00000279099.1","gene_symbol":"AC090740.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35254344,"end":35256605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166450.12","gene_symbol":"PRTG","gene_name":"protogenin [Source:HGNC Symbol;Acc:HGNC:26373]","synonyms":"IGDCC5,FLJ25756","biotype":"protein_coding","ncbi_id":"283659","summary":"This gene encodes a member of the immunoglobulin superfamily. The encoded transmembrane protein has been associated with the development of various tissues, especially neurogenesis. It has been suggested that this gene may be associated with attention deficit hyperactivity disorder (ADHD). [provided by RefSeq, Nov 2014]","start":55611546,"end":55743090,"strand":-1,"description":"protogenin [Source:HGNC Symbol;Acc:HGNC:26373]"}, {"versioned_ensembl_gene_id":"ENSG00000142675.17","gene_symbol":"CNKSR1","gene_name":"connector enhancer of kinase suppressor of Ras 1 [Source:HGNC Symbol;Acc:HGNC:19700]","synonyms":"KSR,CNK1,CNK","biotype":"protein_coding","ncbi_id":"10256","summary":"This gene encodes a protein containing several motifs involved in protein-protein interaction, including PDZ, PH (Pleckstrin homology), and SAM (sterile alpha motif) domains. The encoded protein acts as a scaffold component for receptor tyrosine kinase signaling and may mediate crosstalk between different signaling pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":26177403,"end":26189886,"strand":1,"description":"connector enhancer of kinase suppressor of Ras 1 [Source:HGNC Symbol;Acc:HGNC:19700]"}, {"versioned_ensembl_gene_id":"ENSG00000230594.3","gene_symbol":"CT47A4","gene_name":"cancer/testis antigen family 47, member A4 [Source:HGNC Symbol;Acc:HGNC:33285]","synonyms":"CT47.4","biotype":"protein_coding","ncbi_id":"728075","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120967886,"end":120971208,"strand":-1,"description":"cancer/testis antigen family 47, member A4 [Source:HGNC Symbol;Acc:HGNC:33285]"}, {"versioned_ensembl_gene_id":"ENSG00000018510.13","gene_symbol":"AGPS","gene_name":"alkylglycerone phosphate synthase [Source:HGNC Symbol;Acc:HGNC:327]","synonyms":"ALDHPSY,ADPS,ADHAPS,ADAS,ADAP-S","biotype":"protein_coding","ncbi_id":"8540","summary":"This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome. [provided by RefSeq, Jul 2008]","start":177392644,"end":177559299,"strand":1,"description":"alkylglycerone phosphate synthase [Source:HGNC Symbol;Acc:HGNC:327]"}, {"versioned_ensembl_gene_id":"ENSG00000169953.11","gene_symbol":"HSFY2","gene_name":"heat shock transcription factor, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23950]","synonyms":"FLJ25453","biotype":"protein_coding","ncbi_id":"159119","summary":"This gene encodes a member of the heat shock factor (HSF) family of transcriptional activators for heat shock proteins. This gene is a candidate gene for azoospermia, since it localizes to a region of chromosome Y that is sometimes deleted in infertile males. The genome has two identical copies of this gene within a palindromic region; this record represents the more telomeric copy. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":18731440,"end":18828662,"strand":-1,"description":"heat shock transcription factor, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23950]"}, {"versioned_ensembl_gene_id":"ENSG00000225216.6","gene_symbol":"AC007362.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":205756469,"end":205764006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249501.1","gene_symbol":"USP9YP2","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31742]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387363","summary":null,"start":18776279,"end":18779427,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31742]"}, {"versioned_ensembl_gene_id":"ENSG00000128683.13","gene_symbol":"GAD1","gene_name":"glutamate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:4092]","synonyms":"GAD","biotype":"protein_coding","ncbi_id":"2571","summary":"This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantigen and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome. Deficiency in this enzyme has been shown to lead to pyridoxine dependency with seizures. Alternative splicing of this gene results in two products, the predominant 67-kD form and a less-frequent 25-kD form. [provided by RefSeq, Jul 2008]","start":170813213,"end":170861151,"strand":1,"description":"glutamate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:4092]"}, {"versioned_ensembl_gene_id":"ENSG00000239989.1","gene_symbol":"AC008132.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18794414,"end":18794804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234764.2","gene_symbol":"E2F6P1","gene_name":"E2F transcription factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51449]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"386610","summary":null,"start":18833694,"end":18834438,"strand":1,"description":"E2F transcription factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51449]"}, {"versioned_ensembl_gene_id":"ENSG00000231063.1","gene_symbol":"AC006994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210088226,"end":210089064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231852.6","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"CA21H,P450c21B,CPS1,CYP21B,CAH1,CYP21","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32038265,"end":32041670,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000272807.1","gene_symbol":"AC007038.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":210028417,"end":210029156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255723.1","gene_symbol":"AC108516.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":87317170,"end":87345210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224597.9","gene_symbol":"SVIL-AS1","gene_name":"SVIL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51219]","synonyms":"RP11-534G20.3","biotype":"antisense_RNA","ncbi_id":"102724316","summary":null,"start":29409402,"end":29487745,"strand":1,"description":"SVIL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51219]"}, {"versioned_ensembl_gene_id":"ENSG00000274985.1","gene_symbol":"PTCHD3P1","gene_name":"patched domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44945]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387647","summary":null,"start":29421476,"end":29422012,"strand":-1,"description":"patched domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44945]"}, {"versioned_ensembl_gene_id":"ENSG00000127366.5","gene_symbol":"TAS2R5","gene_name":"taste 2 receptor member 5 [Source:HGNC Symbol;Acc:HGNC:14912]","synonyms":"T2R5","biotype":"protein_coding","ncbi_id":"54429","summary":"This gene encodes a bitter taste receptor; bitter taste receptors are members of the G protein-coupled receptor superfamily and are specifically expressed by taste receptor cells of the tongue and palate epithelia. Each of these apparently intronless taste receptor genes encodes a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered with another 3 candidate taste receptor genes on chromosome 7 and is genetically linked to loci that influence bitter perception. [provided by RefSeq, Jul 2008]","start":141790217,"end":141791367,"strand":1,"description":"taste 2 receptor member 5 [Source:HGNC Symbol;Acc:HGNC:14912]"}, {"versioned_ensembl_gene_id":"ENSG00000227779.1","gene_symbol":"AC234779.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141380823,"end":141381107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225816.1","gene_symbol":"GTF3AP5","gene_name":"general transcription factor IIIA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49748]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128217","summary":null,"start":14985378,"end":14986074,"strand":-1,"description":"general transcription factor IIIA pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49748]"}, {"versioned_ensembl_gene_id":"ENSG00000170537.12","gene_symbol":"TMC7","gene_name":"transmembrane channel like 7 [Source:HGNC Symbol;Acc:HGNC:23000]","synonyms":"FLJ21240","biotype":"protein_coding","ncbi_id":"79905","summary":null,"start":18983934,"end":19063942,"strand":1,"description":"transmembrane channel like 7 [Source:HGNC Symbol;Acc:HGNC:23000]"}, {"versioned_ensembl_gene_id":"ENSG00000163166.14","gene_symbol":"IWS1","gene_name":"IWS1, SUPT6H interacting protein [Source:HGNC Symbol;Acc:HGNC:25467]","synonyms":"FLJ14655,FLJ10006,DKFZp761G0123,FLJ32319","biotype":"protein_coding","ncbi_id":"55677","summary":null,"start":127436207,"end":127526886,"strand":-1,"description":"IWS1, SUPT6H interacting protein [Source:HGNC Symbol;Acc:HGNC:25467]"}, {"versioned_ensembl_gene_id":"ENSG00000121314.2","gene_symbol":"TAS2R8","gene_name":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]","synonyms":"TRB5,T2R8","biotype":"protein_coding","ncbi_id":"50836","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10806051,"end":10807293,"strand":-1,"description":"taste 2 receptor member 8 [Source:HGNC Symbol;Acc:HGNC:14915]"}, {"versioned_ensembl_gene_id":"ENSG00000230271.1","gene_symbol":"AC023141.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57772584,"end":57773199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227047.1","gene_symbol":"AC012065.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20499571,"end":20501311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235061.3","gene_symbol":"UBE2V1P7","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44890]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481746","summary":null,"start":78554412,"end":78554751,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44890]"}, {"versioned_ensembl_gene_id":"ENSG00000223592.2","gene_symbol":"FNDC3CP","gene_name":"fibronectin type III domain containing 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:35452]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100421340","summary":null,"start":78165696,"end":78172422,"strand":-1,"description":"fibronectin type III domain containing 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:35452]"}, {"versioned_ensembl_gene_id":"ENSG00000271788.1","gene_symbol":"AC008875.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43006733,"end":43007543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253461.1","gene_symbol":"IGKV1-35","gene_name":"immunoglobulin kappa variable 1-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5738]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28932","summary":null,"start":89286689,"end":89286973,"strand":-1,"description":"immunoglobulin kappa variable 1-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5738]"}, {"versioned_ensembl_gene_id":"ENSG00000281502.1","gene_symbol":"ASH2LP1","gene_name":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19332]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266703","summary":null,"start":22429412,"end":22430396,"strand":1,"description":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19332]"}, {"versioned_ensembl_gene_id":"ENSG00000233534.1","gene_symbol":"AL035604.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135629405,"end":135630268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275720.1","gene_symbol":"AC243830.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36634069,"end":36634698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236122.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30352597,"end":30353765,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000233911.9","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"MGC22487,Oct4,OCT3,OTF3","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31156880,"end":31163254,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000274602.4","gene_symbol":"PI4KAP1","gene_name":"phosphatidylinositol 4-kinase alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33576]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728233","summary":null,"start":18533646,"end":18577968,"strand":-1,"description":"phosphatidylinositol 4-kinase alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33576]"}, {"versioned_ensembl_gene_id":"ENSG00000276949.1","gene_symbol":"AC011298.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240672530,"end":240672812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278650.1","gene_symbol":"AL158209.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21452197,"end":21452412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214041.4","gene_symbol":"PGAM1P4","gene_name":"phosphoglycerate mutase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42451]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391508","summary":null,"start":9348443,"end":9349192,"strand":1,"description":"phosphoglycerate mutase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42451]"}, {"versioned_ensembl_gene_id":"ENSG00000279280.1","gene_symbol":"AC092364.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21719001,"end":21719670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235884.3","gene_symbol":"LINC00941","gene_name":"long intergenic non-protein coding RNA 941 [Source:HGNC Symbol;Acc:HGNC:48635]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287314","summary":null,"start":30795681,"end":30802711,"strand":1,"description":"long intergenic non-protein coding RNA 941 [Source:HGNC Symbol;Acc:HGNC:48635]"}, {"versioned_ensembl_gene_id":"ENSG00000223661.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":32010892,"end":32018166,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000260362.1","gene_symbol":"AC007218.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9666885,"end":9676843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068912.13","gene_symbol":"ERLEC1","gene_name":"endoplasmic reticulum lectin 1 [Source:HGNC Symbol;Acc:HGNC:25222]","synonyms":"XTP3-B,ERLECTIN,CL25084,C2orf30,XTP3TPB","biotype":"protein_coding","ncbi_id":"27248","summary":"This gene encodes a resident endoplasmic reticulum (ER) protein that functions in N-glycan recognition. This protein is thought to be involved in ER-associated degradation via its interaction with the membrane-associated ubiquitin ligase complex. It also functions as a regulator of multiple cellular stress-response pathways in a manner that promotes metastatic cell survival. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 21. [provided by RefSeq, Aug 2011]","start":53787044,"end":53818819,"strand":1,"description":"endoplasmic reticulum lectin 1 [Source:HGNC Symbol;Acc:HGNC:25222]"}, {"versioned_ensembl_gene_id":"ENSG00000251163.1","gene_symbol":"PRELID3BP4","gene_name":"PRELI domain containing 3B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420275","summary":null,"start":42897262,"end":42897832,"strand":-1,"description":"PRELI domain containing 3B pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49066]"}, {"versioned_ensembl_gene_id":"ENSG00000214102.7","gene_symbol":"WEE2","gene_name":"WEE1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:19684]","synonyms":"FLJ16107","biotype":"protein_coding","ncbi_id":"494551","summary":null,"start":141708353,"end":141731271,"strand":1,"description":"WEE1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:19684]"}, {"versioned_ensembl_gene_id":"ENSG00000279328.1","gene_symbol":"AC073439.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126432796,"end":126434569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282752.1","gene_symbol":"CTDP1","gene_name":"CTD phosphatase subunit 1 [Source:HGNC Symbol;Acc:HGNC:2498]","synonyms":"FCP1","biotype":"protein_coding","ncbi_id":"9150","summary":"This gene encodes a protein which interacts with the carboxy-terminus of the RAP74 subunit of transcription initiation factor TFIIF, and functions as a phosphatase that processively dephosphorylates the C-terminus of POLR2A (a subunit of RNA polymerase II), making it available for initiation of gene expression. Mutations in this gene are associated with congenital cataracts, facial dysmorphism and neuropathy syndrome (CCFDN). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":79685555,"end":79723770,"strand":1,"description":"CTD phosphatase subunit 1 [Source:HGNC Symbol;Acc:HGNC:2498]"}, {"versioned_ensembl_gene_id":"ENSG00000139220.16","gene_symbol":"PPFIA2","gene_name":"PTPRF interacting protein alpha 2 [Source:HGNC Symbol;Acc:HGNC:9246]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8499","summary":"The protein encoded by this gene is a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. Liprins interact with members of LAR family of transmembrane protein tyrosine phosphatases, which are known to be important for axon guidance and mammary gland development. It has been proposed that liprins are multivalent proteins that form complex structures and act as scaffolds for the recruitment and anchoring of LAR family of tyrosine phosphatases. This protein has been shown to bind the calcium/calmodulin-dependent serine protein kinase (MAGUK family) protein (also known as CASK) and proposed to regulate higher-order brain functions in mammals. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":81257975,"end":81759553,"strand":-1,"description":"PTPRF interacting protein alpha 2 [Source:HGNC Symbol;Acc:HGNC:9246]"}, {"versioned_ensembl_gene_id":"ENSG00000135454.13","gene_symbol":"B4GALNT1","gene_name":"beta-1,4-N-acetyl-galactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4117]","synonyms":"SPG26,GALGT,beta1-4GalNAc-T","biotype":"protein_coding","ncbi_id":"2583","summary":"GM2 and GD2 gangliosides are sialic acid-containing glycosphingolipids. GalNAc-T is the enzyme involved in the biosynthesis of G(M2) and G(D2) glycosphingolipids. GalNAc-T catalyzes the transfer of GalNAc into G(M3) and G(D3) by a beta-1,4 linkage, resulting in the synthesis of G(M2) and G(D2), respectively. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":57623410,"end":57633355,"strand":-1,"description":"beta-1,4-N-acetyl-galactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4117]"}, {"versioned_ensembl_gene_id":"ENSG00000232604.1","gene_symbol":"AC010967.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52864235,"end":52866631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281945.1","gene_symbol":"AC127518.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82978708,"end":82981921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228033.5","gene_symbol":"AC010967.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52722677,"end":52910020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232930.1","gene_symbol":"AC083864.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36029611,"end":36055431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115665.8","gene_symbol":"SLC5A7","gene_name":"solute carrier family 5 member 7 [Source:HGNC Symbol;Acc:HGNC:14025]","synonyms":"hCHT,CHT1","biotype":"protein_coding","ncbi_id":"60482","summary":"This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":107986523,"end":108013994,"strand":1,"description":"solute carrier family 5 member 7 [Source:HGNC Symbol;Acc:HGNC:14025]"}, {"versioned_ensembl_gene_id":"ENSG00000089154.10","gene_symbol":"GCN1","gene_name":"GCN1, eIF2 alpha kinase activator homolog [Source:HGNC Symbol;Acc:HGNC:4199]","synonyms":"KIAA0219,GCN1L1,GCN1L","biotype":"protein_coding","ncbi_id":"10985","summary":null,"start":120127203,"end":120194710,"strand":-1,"description":"GCN1, eIF2 alpha kinase activator homolog [Source:HGNC Symbol;Acc:HGNC:4199]"}, {"versioned_ensembl_gene_id":"ENSG00000180712.3","gene_symbol":"LINC02363","gene_name":"long intergenic non-protein coding RNA 2363 [Source:HGNC Symbol;Acc:HGNC:53286]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728175","summary":null,"start":184340756,"end":184353977,"strand":-1,"description":"long intergenic non-protein coding RNA 2363 [Source:HGNC Symbol;Acc:HGNC:53286]"}, {"versioned_ensembl_gene_id":"ENSG00000227765.4","gene_symbol":"MYL12BP2","gene_name":"myosin light chain 12B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51650]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391722","summary":null,"start":184299129,"end":184299640,"strand":-1,"description":"myosin light chain 12B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51650]"}, {"versioned_ensembl_gene_id":"ENSG00000221821.3","gene_symbol":"C6orf226","gene_name":"chromosome 6 open reading frame 226 [Source:HGNC Symbol;Acc:HGNC:34431]","synonyms":"LOC441150","biotype":"protein_coding","ncbi_id":"441150","summary":null,"start":42890265,"end":42890816,"strand":-1,"description":"chromosome 6 open reading frame 226 [Source:HGNC Symbol;Acc:HGNC:34431]"}, {"versioned_ensembl_gene_id":"ENSG00000171703.16","gene_symbol":"TCEA2","gene_name":"transcription elongation factor A2 [Source:HGNC Symbol;Acc:HGNC:11614]","synonyms":"TFIIS","biotype":"protein_coding","ncbi_id":"6919","summary":"The protein encoded by this gene is found in the nucleus, where it functions as an SII class transcription elongation factor. Elongation factors in this class are responsible for releasing RNA polymerase II ternary complexes from transcriptional arrest at template-encoded arresting sites. The encoded protein has been shown to interact with general transcription factor IIB, a basal transcription factor. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":64049836,"end":64072347,"strand":1,"description":"transcription elongation factor A2 [Source:HGNC Symbol;Acc:HGNC:11614]"}, {"versioned_ensembl_gene_id":"ENSG00000249532.5","gene_symbol":"AC106864.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112646476,"end":112650051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249634.1","gene_symbol":"USP9YP5","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38418]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421217","summary":null,"start":18490915,"end":18494295,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38418]"}, {"versioned_ensembl_gene_id":"ENSG00000282169.1","gene_symbol":"AC243913.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28563475,"end":28563679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274616.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3H,NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156191,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000196917.5","gene_symbol":"HCAR1","gene_name":"hydroxycarboxylic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:4532]","synonyms":"TA-GPCR,LACR1,HCA1,GPR81,GPR104,FKSG80","biotype":"protein_coding","ncbi_id":"27198","summary":"G protein-coupled receptors (GPCRs, or GPRs), such as GPR81, contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins.[supplied by OMIM, Feb 2005]","start":122726076,"end":122730843,"strand":-1,"description":"hydroxycarboxylic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:4532]"}, {"versioned_ensembl_gene_id":"ENSG00000169330.8","gene_symbol":"KIAA1024","gene_name":"KIAA1024 [Source:HGNC Symbol;Acc:HGNC:29172]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23251","summary":null,"start":79432516,"end":79472290,"strand":1,"description":"KIAA1024 [Source:HGNC Symbol;Acc:HGNC:29172]"}, {"versioned_ensembl_gene_id":"ENSG00000100097.11","gene_symbol":"LGALS1","gene_name":"galectin 1 [Source:HGNC Symbol;Acc:HGNC:6561]","synonyms":"GBP","biotype":"protein_coding","ncbi_id":"3956","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. This gene product may act as an autocrine negative growth factor that regulates cell proliferation. [provided by RefSeq, Jul 2008]","start":37675608,"end":37679806,"strand":1,"description":"galectin 1 [Source:HGNC Symbol;Acc:HGNC:6561]"}, {"versioned_ensembl_gene_id":"ENSG00000134186.11","gene_symbol":"PRPF38B","gene_name":"pre-mRNA processing factor 38B [Source:HGNC Symbol;Acc:HGNC:25512]","synonyms":"NET1,FLJ10330","biotype":"protein_coding","ncbi_id":"55119","summary":null,"start":108692323,"end":108701803,"strand":1,"description":"pre-mRNA processing factor 38B [Source:HGNC Symbol;Acc:HGNC:25512]"}, {"versioned_ensembl_gene_id":"ENSG00000261431.1","gene_symbol":"AL023803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38961925,"end":38962111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128692.8","gene_symbol":"EIF2S2P4","gene_name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37626]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728350","summary":null,"start":170751805,"end":170752788,"strand":1,"description":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37626]"}, {"versioned_ensembl_gene_id":"ENSG00000225813.1","gene_symbol":"AC009299.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161281902,"end":161282618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259673.5","gene_symbol":"IQCH-AS1","gene_name":"IQCH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44104]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506686","summary":null,"start":67403619,"end":67521844,"strand":-1,"description":"IQCH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44104]"}, {"versioned_ensembl_gene_id":"ENSG00000177646.18","gene_symbol":"ACAD9","gene_name":"acyl-CoA dehydrogenase family member 9 [Source:HGNC Symbol;Acc:HGNC:21497]","synonyms":"NPD002,MGC14452","biotype":"protein_coding","ncbi_id":"28976","summary":"This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]","start":128879596,"end":128916067,"strand":1,"description":"acyl-CoA dehydrogenase family member 9 [Source:HGNC Symbol;Acc:HGNC:21497]"}, {"versioned_ensembl_gene_id":"ENSG00000242634.1","gene_symbol":"RPS24P16","gene_name":"ribosomal protein S24 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216340","summary":null,"start":67232446,"end":67232837,"strand":1,"description":"ribosomal protein S24 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35542]"}, {"versioned_ensembl_gene_id":"ENSG00000234619.1","gene_symbol":"RPL7P11","gene_name":"ribosomal protein L7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35667]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270823","summary":null,"start":8750430,"end":8751087,"strand":1,"description":"ribosomal protein L7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35667]"}, {"versioned_ensembl_gene_id":"ENSG00000230552.5","gene_symbol":"AC092162.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176724268,"end":176819310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107796.13","gene_symbol":"ACTA2","gene_name":"actin, alpha 2, smooth muscle, aorta [Source:HGNC Symbol;Acc:HGNC:130]","synonyms":"ACTSA","biotype":"protein_coding","ncbi_id":"59","summary":"This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a smooth muscle actin that is involved in vascular contractility and blood pressure homeostasis. Mutations in this gene cause a variety of vascular diseases, such as thoracic aortic disease, coronary artery disease, stroke, and Moyamoya disease, as well as multisystemic smooth muscle dysfunction syndrome. [provided by RefSeq, Sep 2017]","start":88935074,"end":88991339,"strand":-1,"description":"actin, alpha 2, smooth muscle, aorta [Source:HGNC Symbol;Acc:HGNC:130]"}, {"versioned_ensembl_gene_id":"ENSG00000224212.4","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32823186,"end":32831955,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000268650.3","gene_symbol":"AC005759.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18204730,"end":18220480,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179342.4","gene_symbol":"AC008267.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66505155,"end":66506223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237311.1","gene_symbol":"AL034397.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65999751,"end":66001071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231809.4","gene_symbol":"NANOGP9","gene_name":"Nanog homeobox pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"349386","summary":null,"start":65772741,"end":65773632,"strand":-1,"description":"Nanog homeobox pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23107]"}, {"versioned_ensembl_gene_id":"ENSG00000244055.1","gene_symbol":"AC007566.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92457564,"end":92491610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278293.2","gene_symbol":"IGLV7-43","gene_name":"immunoglobulin lambda variable 7-43 [Source:HGNC Symbol;Acc:HGNC:5929]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28776","summary":null,"start":22395019,"end":22395490,"strand":1,"description":"immunoglobulin lambda variable 7-43 [Source:HGNC Symbol;Acc:HGNC:5929]"}, {"versioned_ensembl_gene_id":"ENSG00000253162.1","gene_symbol":"AC026991.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3373353,"end":3375226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114439.18","gene_symbol":"BBX","gene_name":"BBX, HMG-box containing [Source:HGNC Symbol;Acc:HGNC:14422]","synonyms":"MDS001,HSPC339,HBP2","biotype":"protein_coding","ncbi_id":"56987","summary":null,"start":107522936,"end":107811324,"strand":1,"description":"BBX, HMG-box containing [Source:HGNC Symbol;Acc:HGNC:14422]"}, {"versioned_ensembl_gene_id":"ENSG00000258121.1","gene_symbol":"AC089987.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48483287,"end":48500961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189403.14","gene_symbol":"HMGB1","gene_name":"high mobility group box 1 [Source:HGNC Symbol;Acc:HGNC:4983]","synonyms":"SBP-1,HMG3,HMG1,DKFZp686A04236","biotype":"protein_coding","ncbi_id":"3146","summary":"This gene encodes a protein that belongs to the High Mobility Group-box superfamily. The encoded non-histone, nuclear DNA-binding protein regulates transcription, and is involved in organization of DNA. This protein plays a role in several cellular processes, including inflammation, cell differentiation and tumor cell migration. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2015]","start":30456704,"end":30617597,"strand":-1,"description":"high mobility group box 1 [Source:HGNC Symbol;Acc:HGNC:4983]"}, {"versioned_ensembl_gene_id":"ENSG00000215089.3","gene_symbol":"KRT18P11","gene_name":"keratin 18 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6431]","synonyms":"KRT18L1","biotype":"processed_pseudogene","ncbi_id":"3876","summary":null,"start":92459670,"end":92460952,"strand":1,"description":"keratin 18 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6431]"}, {"versioned_ensembl_gene_id":"ENSG00000228582.9","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"D6S217E,RING11,ABCB3,PSF2","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32744153,"end":32761098,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000180209.11","gene_symbol":"MYLPF","gene_name":"myosin light chain, phosphorylatable, fast skeletal muscle [Source:HGNC Symbol;Acc:HGNC:29824]","synonyms":"MYL11,MRLC2,HUMMLC2B","biotype":"protein_coding","ncbi_id":"29895","summary":null,"start":30370934,"end":30377991,"strand":1,"description":"myosin light chain, phosphorylatable, fast skeletal muscle [Source:HGNC Symbol;Acc:HGNC:29824]"}, {"versioned_ensembl_gene_id":"ENSG00000130520.10","gene_symbol":"LSM4","gene_name":"LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17259]","synonyms":"YER112W","biotype":"protein_coding","ncbi_id":"25804","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":18306230,"end":18323274,"strand":-1,"description":"LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17259]"}, {"versioned_ensembl_gene_id":"ENSG00000116698.21","gene_symbol":"SMG7","gene_name":"SMG7, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:16792]","synonyms":"SMG-7,SGA56M,KIAA0250,EST1C,C1orf16","biotype":"protein_coding","ncbi_id":"9887","summary":"This gene encodes a protein that is essential for nonsense-mediated mRNA decay (NMD); a process whereby transcripts with premature termination codons are targeted for rapid degradation by a mRNA decay complex. The mRNA decay complex consists, in part, of this protein along with proteins SMG5 and UPF1. The N-terminal domain of this protein is thought to mediate its association with SMG5 or UPF1 while the C-terminal domain interacts with the mRNA decay complex. This protein may therefore couple changes in UPF1 phosphorylation state to the degradation of NMD-candidate transcripts. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2011]","start":183472216,"end":183598246,"strand":1,"description":"SMG7, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:16792]"}, {"versioned_ensembl_gene_id":"ENSG00000272330.1","gene_symbol":"AC002044.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73014319,"end":73014476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176422.13","gene_symbol":"SPRYD4","gene_name":"SPRY domain containing 4 [Source:HGNC Symbol;Acc:HGNC:27468]","synonyms":"DKFZp686N0877","biotype":"protein_coding","ncbi_id":"283377","summary":null,"start":56468567,"end":56479707,"strand":1,"description":"SPRY domain containing 4 [Source:HGNC Symbol;Acc:HGNC:27468]"}, {"versioned_ensembl_gene_id":"ENSG00000101544.8","gene_symbol":"ADNP2","gene_name":"ADNP homeobox 2 [Source:HGNC Symbol;Acc:HGNC:23803]","synonyms":"ZNF508,KIAA0863","biotype":"protein_coding","ncbi_id":"22850","summary":null,"start":80109031,"end":80147523,"strand":1,"description":"ADNP homeobox 2 [Source:HGNC Symbol;Acc:HGNC:23803]"}, {"versioned_ensembl_gene_id":"ENSG00000085719.12","gene_symbol":"CPNE3","gene_name":"copine 3 [Source:HGNC Symbol;Acc:HGNC:2316]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8895","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene encodes a protein which contains two type II C2 domains in the amino-terminus and an A domain-like sequence in the carboxy-terminus. The A domain mediates interactions between integrins and extracellular ligands. [provided by RefSeq, Aug 2008]","start":86514427,"end":86561498,"strand":1,"description":"copine 3 [Source:HGNC Symbol;Acc:HGNC:2316]"}, {"versioned_ensembl_gene_id":"ENSG00000241048.1","gene_symbol":"AC117386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150202174,"end":150225190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231876.7","gene_symbol":"AC009158.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26302064,"end":26334428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237309.1","gene_symbol":"MTND2P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42107]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873177","summary":null,"start":57186412,"end":57187441,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42107]"}, {"versioned_ensembl_gene_id":"ENSG00000233083.1","gene_symbol":"FTH1P6","gene_name":"ferritin heavy chain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39088]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481787","summary":null,"start":52629743,"end":52630078,"strand":1,"description":"ferritin heavy chain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39088]"}, {"versioned_ensembl_gene_id":"ENSG00000282102.1","gene_symbol":"IGHD5-12","gene_name":"immunoglobulin heavy diversity 5-12 [Source:HGNC Symbol;Acc:HGNC:5508]","synonyms":"IGHD512,DK1","biotype":"IG_D_gene","ncbi_id":"28491","summary":null,"start":105903420,"end":105903442,"strand":-1,"description":"immunoglobulin heavy diversity 5-12 [Source:HGNC Symbol;Acc:HGNC:5508]"}, {"versioned_ensembl_gene_id":"ENSG00000249833.5","gene_symbol":"CCDC37-AS1","gene_name":"CCDC37 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49641]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506907","summary":null,"start":126393032,"end":126394851,"strand":-1,"description":"CCDC37 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49641]"}, {"versioned_ensembl_gene_id":"ENSG00000255410.1","gene_symbol":"AC091564.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6630603,"end":6635208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198925.10","gene_symbol":"ATG9A","gene_name":"autophagy related 9A [Source:HGNC Symbol;Acc:HGNC:22408]","synonyms":"FLJ22169,APG9L1","biotype":"protein_coding","ncbi_id":"79065","summary":null,"start":219209772,"end":219229717,"strand":-1,"description":"autophagy related 9A [Source:HGNC Symbol;Acc:HGNC:22408]"}, {"versioned_ensembl_gene_id":"ENSG00000243033.2","gene_symbol":"GAPDHP47","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:37803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240712","summary":null,"start":143503275,"end":143504273,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:37803]"}, {"versioned_ensembl_gene_id":"ENSG00000280559.1","gene_symbol":"AC106795.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177870853,"end":177871194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281668.1","gene_symbol":"IGKV1OR2-118","gene_name":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]","synonyms":"IGKV1/OR2-118","biotype":"IG_V_pseudogene","ncbi_id":"339562","summary":null,"start":90315366,"end":90315836,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-118 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:37488]"}, {"versioned_ensembl_gene_id":"ENSG00000267794.1","gene_symbol":"AP001120.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11618208,"end":11618315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120162.9","gene_symbol":"MOB3B","gene_name":"MOB kinase activator 3B [Source:HGNC Symbol;Acc:HGNC:23825]","synonyms":"MOBKL2B,MOB1D,FLJ13204,C9orf35","biotype":"protein_coding","ncbi_id":"79817","summary":"The protein encoded by this gene shares similarity with the yeast Mob1 protein. Yeast Mob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. This gene is located on the opposite strand as the interferon kappa precursor (IFNK) gene. [provided by RefSeq, Jul 2008]","start":27325209,"end":27529781,"strand":-1,"description":"MOB kinase activator 3B [Source:HGNC Symbol;Acc:HGNC:23825]"}, {"versioned_ensembl_gene_id":"ENSG00000204592.8","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30489467,"end":30494205,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000257792.1","gene_symbol":"AC090115.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48394510,"end":48395392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275050.4","gene_symbol":"ZNF66","gene_name":"zinc finger protein 66 [Source:HGNC Symbol;Acc:HGNC:13135]","synonyms":"FLJ16537,ZNF66P","biotype":"protein_coding","ncbi_id":"7617","summary":null,"start":20776304,"end":20807420,"strand":1,"description":"zinc finger protein 66 [Source:HGNC Symbol;Acc:HGNC:13135]"}, {"versioned_ensembl_gene_id":"ENSG00000178623.11","gene_symbol":"GPR35","gene_name":"G protein-coupled receptor 35 [Source:HGNC Symbol;Acc:HGNC:4492]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2859","summary":null,"start":240605431,"end":240631259,"strand":1,"description":"G protein-coupled receptor 35 [Source:HGNC Symbol;Acc:HGNC:4492]"}, {"versioned_ensembl_gene_id":"ENSG00000260404.3","gene_symbol":"AC110079.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":118591773,"end":118633729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159128.14","gene_symbol":"IFNGR2","gene_name":"interferon gamma receptor 2 [Source:HGNC Symbol;Acc:HGNC:5440]","synonyms":"AF-1,IFNGT1","biotype":"protein_coding","ncbi_id":"3460","summary":"This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008]","start":33402896,"end":33479348,"strand":1,"description":"interferon gamma receptor 2 [Source:HGNC Symbol;Acc:HGNC:5440]"}, {"versioned_ensembl_gene_id":"ENSG00000120159.11","gene_symbol":"CAAP1","gene_name":"caspase activity and apoptosis inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:25834]","synonyms":"FLJ13657,CAAP,C9orf82","biotype":"protein_coding","ncbi_id":"79886","summary":null,"start":26840685,"end":26892804,"strand":-1,"description":"caspase activity and apoptosis inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:25834]"}, {"versioned_ensembl_gene_id":"ENSG00000230118.1","gene_symbol":"AC092569.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30746444,"end":30746701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008277.14","gene_symbol":"ADAM22","gene_name":"ADAM metallopeptidase domain 22 [Source:HGNC Symbol;Acc:HGNC:201]","synonyms":"MDC2","biotype":"protein_coding","ncbi_id":"53616","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. Unlike other members of the ADAM protein family, the protein encoded by this gene lacks metalloprotease activity since it has no zinc-binding motif. This gene is highly expressed in the brain and may function as an integrin ligand in the brain. In mice, it has been shown to be essential for correct myelination in the peripheral nervous system. Alternative splicing results in several transcript variants.[provided by RefSeq, Dec 2010]","start":87934143,"end":88202889,"strand":1,"description":"ADAM metallopeptidase domain 22 [Source:HGNC Symbol;Acc:HGNC:201]"}, {"versioned_ensembl_gene_id":"ENSG00000184162.14","gene_symbol":"NR2C2AP","gene_name":"nuclear receptor 2C2 associated protein [Source:HGNC Symbol;Acc:HGNC:30763]","synonyms":"TRA16","biotype":"protein_coding","ncbi_id":"126382","summary":null,"start":19201416,"end":19203424,"strand":-1,"description":"nuclear receptor 2C2 associated protein [Source:HGNC Symbol;Acc:HGNC:30763]"}, {"versioned_ensembl_gene_id":"ENSG00000230451.2","gene_symbol":"RPS29P6","gene_name":"ribosomal protein S29 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270903","summary":null,"start":37330852,"end":37330996,"strand":1,"description":"ribosomal protein S29 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35718]"}, {"versioned_ensembl_gene_id":"ENSG00000226166.2","gene_symbol":"AC244670.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12692909,"end":12693020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281591.1","gene_symbol":"DBET","gene_name":"D4Z4 binding element transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43904]","synonyms":"DUX4L30,DBE-T","biotype":"lincRNA","ncbi_id":"100419743","summary":null,"start":190064502,"end":190067864,"strand":1,"description":"D4Z4 binding element transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43904]"}, {"versioned_ensembl_gene_id":"ENSG00000236110.1","gene_symbol":"OR2AM1P","gene_name":"olfactory receptor family 2 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15113]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81366","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":36021692,"end":36022113,"strand":1,"description":"olfactory receptor family 2 subfamily AM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15113]"}, {"versioned_ensembl_gene_id":"ENSG00000204518.2","gene_symbol":"AADACL4","gene_name":"arylacetamide deacetylase like 4 [Source:HGNC Symbol;Acc:HGNC:32038]","synonyms":"OTTHUMG00000001889","biotype":"protein_coding","ncbi_id":"343066","summary":null,"start":12644547,"end":12667086,"strand":1,"description":"arylacetamide deacetylase like 4 [Source:HGNC Symbol;Acc:HGNC:32038]"}, {"versioned_ensembl_gene_id":"ENSG00000230265.1","gene_symbol":"AC079178.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26557675,"end":26558330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226611.2","gene_symbol":"OFD1P2Y","gene_name":"OFD1 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:23874]","synonyms":"OFDYP2,OFD1PY2,OFD1P2","biotype":"unprocessed_pseudogene","ncbi_id":"378010","summary":null,"start":18080681,"end":18096202,"strand":-1,"description":"OFD1 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:23874]"}, {"versioned_ensembl_gene_id":"ENSG00000230412.1","gene_symbol":"ELOCP12","gene_name":"elongin C pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38148]","synonyms":"TCEB1P12","biotype":"processed_pseudogene","ncbi_id":"100462874","summary":null,"start":18068483,"end":18068810,"strand":1,"description":"elongin C pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38148]"}, {"versioned_ensembl_gene_id":"ENSG00000168234.12","gene_symbol":"TTC39C","gene_name":"tetratricopeptide repeat domain 39C [Source:HGNC Symbol;Acc:HGNC:26595]","synonyms":"HsT2697,FLJ33761,C18orf17","biotype":"protein_coding","ncbi_id":"125488","summary":null,"start":23992773,"end":24135610,"strand":1,"description":"tetratricopeptide repeat domain 39C [Source:HGNC Symbol;Acc:HGNC:26595]"}, {"versioned_ensembl_gene_id":"ENSG00000274174.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7,PYPAF3,NALP7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54594345,"end":54618340,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000275771.1","gene_symbol":"AC140725.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101937591,"end":101938470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164900.4","gene_symbol":"GBX1","gene_name":"gastrulation brain homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4185]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2636","summary":null,"start":151148589,"end":151174745,"strand":-1,"description":"gastrulation brain homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4185]"}, {"versioned_ensembl_gene_id":"ENSG00000080371.5","gene_symbol":"RAB21","gene_name":"RAB21, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18263]","synonyms":"KIAA0118","biotype":"protein_coding","ncbi_id":"23011","summary":"This gene belongs to the Rab family of monomeric GTPases, which are involved in the control of cellular membrane traffic. The encoded protein plays a role in the targeted trafficking of integrins via its association with integrin alpha tails. As a consequence, the encoded protein is involved in the regulation of cell adhesion and migration. Expression of this gene is associated with a poor prognosis for glioma patients. This gene is downregulated by the tumor suppressor miR-200b, and miRNA-200b is itself downregulated in glioma tissues. [provided by RefSeq, Nov 2015]","start":71754874,"end":71800285,"strand":1,"description":"RAB21, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18263]"}, {"versioned_ensembl_gene_id":"ENSG00000234481.1","gene_symbol":"AC117945.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36773140,"end":36775768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279499.1","gene_symbol":"AL157770.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30196443,"end":30196881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259747.1","gene_symbol":"AC104261.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38671847,"end":38689191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258273.1","gene_symbol":"AC024257.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48333755,"end":48333901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125816.4","gene_symbol":"NKX2-4","gene_name":"NK2 homeobox 4 [Source:HGNC Symbol;Acc:HGNC:7837]","synonyms":"NKX2D,NKX2.4","biotype":"protein_coding","ncbi_id":"644524","summary":null,"start":21395367,"end":21398028,"strand":-1,"description":"NK2 homeobox 4 [Source:HGNC Symbol;Acc:HGNC:7837]"}, {"versioned_ensembl_gene_id":"ENSG00000254261.1","gene_symbol":"AL451137.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26746953,"end":26786874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274232.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54811737,"end":54822719,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000251644.1","gene_symbol":"HPRT1P1","gene_name":"hypoxanthine phosphoribosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130067","summary":null,"start":15864938,"end":15865940,"strand":-1,"description":"hypoxanthine phosphoribosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51622]"}, {"versioned_ensembl_gene_id":"ENSG00000230706.2","gene_symbol":"AL035246.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88061590,"end":88062844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282342.1","gene_symbol":"IGHJ2","gene_name":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28481","summary":null,"start":105865970,"end":105866022,"strand":-1,"description":"immunoglobulin heavy joining 2 [Source:HGNC Symbol;Acc:HGNC:5534]"}, {"versioned_ensembl_gene_id":"ENSG00000271056.1","gene_symbol":"AL136363.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87807549,"end":87809883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156256.14","gene_symbol":"USP16","gene_name":"ubiquitin specific peptidase 16 [Source:HGNC Symbol;Acc:HGNC:12614]","synonyms":"Ubp-M","biotype":"protein_coding","ncbi_id":"10600","summary":"This gene encodes a deubiquitinating enzyme that is phosphorylated at the onset of mitosis and then dephosphorylated at the metaphase/anaphase transition. It can deubiquitinate H2A, one of two major ubiquitinated proteins of chromatin, in vitro and a mutant form of the protein was shown to block cell division. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":29024629,"end":29054488,"strand":1,"description":"ubiquitin specific peptidase 16 [Source:HGNC Symbol;Acc:HGNC:12614]"}, {"versioned_ensembl_gene_id":"ENSG00000100473.15","gene_symbol":"COCH","gene_name":"cochlin [Source:HGNC Symbol;Acc:HGNC:2180]","synonyms":"DFNA9,DFNA31,COCH-5B2","biotype":"protein_coding","ncbi_id":"1690","summary":"The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated. [provided by RefSeq, Oct 2008]","start":30874514,"end":30895065,"strand":1,"description":"cochlin [Source:HGNC Symbol;Acc:HGNC:2180]"}, {"versioned_ensembl_gene_id":"ENSG00000233403.1","gene_symbol":"AC121342.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25878339,"end":25893544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279139.1","gene_symbol":"AC098679.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":158109500,"end":158110153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279994.1","gene_symbol":"AC017037.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":157945817,"end":157946642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276155.4","gene_symbol":"MAPT","gene_name":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]","synonyms":"MAPTL,PPND,FTDP-17,MTBT2,FLJ31424,MTBT1,DDPAC,MSTD,tau,MGC138549,PPP1R103","biotype":"protein_coding","ncbi_id":"4137","summary":"This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008]","start":46069784,"end":46203150,"strand":-1,"description":"microtubule associated protein tau [Source:HGNC Symbol;Acc:HGNC:6893]"}, {"versioned_ensembl_gene_id":"ENSG00000257572.1","gene_symbol":"AC008127.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45071769,"end":45072843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171951.4","gene_symbol":"SCG2","gene_name":"secretogranin II [Source:HGNC Symbol;Acc:HGNC:10575]","synonyms":"CHGC,SN,SgII","biotype":"protein_coding","ncbi_id":"7857","summary":"The protein encoded by this gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. Studies in rodents suggest that the full-length protein, secretogranin II, is involved in the packaging or sorting of peptide hormones and neuropeptides into secretory vesicles. The full-length protein is cleaved to produce the active peptide secretoneurin, which exerts chemotaxic effects on specific cell types, and EM66, whose function is unknown. [provided by RefSeq, Jul 2008]","start":223596940,"end":223602503,"strand":-1,"description":"secretogranin II [Source:HGNC Symbol;Acc:HGNC:10575]"}, {"versioned_ensembl_gene_id":"ENSG00000184719.11","gene_symbol":"RNLS","gene_name":"renalase, FAD dependent amine oxidase [Source:HGNC Symbol;Acc:HGNC:25641]","synonyms":"renalase,FLJ11218,C10orf59","biotype":"protein_coding","ncbi_id":"55328","summary":"Renalase is a flavin adenine dinucleotide-dependent amine oxidase that is secreted into the blood from the kidney (Xu et al., 2005 [PubMed 15841207]).[supplied by OMIM, Mar 2008]","start":88273864,"end":88584530,"strand":-1,"description":"renalase, FAD dependent amine oxidase [Source:HGNC Symbol;Acc:HGNC:25641]"}, {"versioned_ensembl_gene_id":"ENSG00000224441.1","gene_symbol":"AC068831.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90932586,"end":90935130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165732.12","gene_symbol":"DDX21","gene_name":"DExD-box helicase 21 [Source:HGNC Symbol;Acc:HGNC:2744]","synonyms":"RH-II/GU,GURDB","biotype":"protein_coding","ncbi_id":"9188","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an antigen recognized by autoimmune antibodies from a patient with watermelon stomach disease. This protein unwinds double-stranded RNA, folds single-stranded RNA, and may play important roles in ribosomal RNA biogenesis, RNA editing, RNA transport, and general transcription. [provided by RefSeq, Jul 2008]","start":68956128,"end":68985073,"strand":1,"description":"DExD-box helicase 21 [Source:HGNC Symbol;Acc:HGNC:2744]"}, {"versioned_ensembl_gene_id":"ENSG00000228748.2","gene_symbol":"AL450306.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77782866,"end":77793176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225076.1","gene_symbol":"WWC3-AS1","gene_name":"WWC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41236]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873953","summary":null,"start":10024842,"end":10038654,"strand":-1,"description":"WWC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41236]"}, {"versioned_ensembl_gene_id":"ENSG00000235295.1","gene_symbol":"LINC01634","gene_name":"long intergenic non-protein coding RNA 1634 [Source:HGNC Symbol;Acc:HGNC:52421]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100192420","summary":null,"start":18029385,"end":18037968,"strand":1,"description":"long intergenic non-protein coding RNA 1634 [Source:HGNC Symbol;Acc:HGNC:52421]"}, {"versioned_ensembl_gene_id":"ENSG00000241218.1","gene_symbol":"AC063944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107327830,"end":107329197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173020.10","gene_symbol":"GRK2","gene_name":"G protein-coupled receptor kinase 2 [Source:HGNC Symbol;Acc:HGNC:289]","synonyms":"BARK1,ADRBK1","biotype":"protein_coding","ncbi_id":"156","summary":"This gene encodes a member of the G protein-coupled receptor kinase family of proteins. The encoded protein phosphorylates the beta-adrenergic receptor as well as a wide range of other substrates including non-GPCR cell surface receptors, and cytoskeletal, mitochondrial, and transcription factor proteins. Data from rodent models supports a role for this gene in embryonic development, heart function and metabolism. Elevated expression of this gene has been observed in human patients with heart failure and Alzheimer's disease. [provided by RefSeq, Sep 2017]","start":67266410,"end":67286556,"strand":1,"description":"G protein-coupled receptor kinase 2 [Source:HGNC Symbol;Acc:HGNC:289]"}, {"versioned_ensembl_gene_id":"ENSG00000233589.1","gene_symbol":"AL138789.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68479129,"end":68483539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185418.15","gene_symbol":"TARSL2","gene_name":"threonyl-tRNA synthetase like 2 [Source:HGNC Symbol;Acc:HGNC:24728]","synonyms":"FLJ25005","biotype":"protein_coding","ncbi_id":"123283","summary":null,"start":101653598,"end":101724604,"strand":-1,"description":"threonyl-tRNA synthetase like 2 [Source:HGNC Symbol;Acc:HGNC:24728]"}, {"versioned_ensembl_gene_id":"ENSG00000278372.4","gene_symbol":"MYO19","gene_name":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]","synonyms":"FLJ22865,MYOHD1","biotype":"protein_coding","ncbi_id":"80179","summary":null,"start":36496005,"end":36543807,"strand":-1,"description":"myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]"}, {"versioned_ensembl_gene_id":"ENSG00000101197.12","gene_symbol":"BIRC7","gene_name":"baculoviral IAP repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:13702]","synonyms":"KIAP,RNF50,mliap,ML-IAP","biotype":"protein_coding","ncbi_id":"79444","summary":"This gene encodes a member of the inhibitor of apoptosis protein (IAP) family, and contains a single copy of a baculovirus IAP repeat (BIR) as well as a RING-type zinc finger domain. The BIR domain is essential for inhibitory activity and interacts with caspases, while the RING finger domain sometimes enhances antiapoptotic activity but does not inhibit apoptosis alone. Elevated levels of the encoded protein may be associated with cancer progression and play a role in chemotherapy sensitivity. Alternative splicing results in multiple transcript variants [provided by RefSeq, Jul 2013]","start":63235883,"end":63240507,"strand":1,"description":"baculoviral IAP repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:13702]"}, {"versioned_ensembl_gene_id":"ENSG00000251112.2","gene_symbol":"AC106794.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12794100,"end":12794731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250855.1","gene_symbol":"AC139718.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111802801,"end":111839886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174327.6","gene_symbol":"SLC16A13","gene_name":"solute carrier family 16 member 13 [Source:HGNC Symbol;Acc:HGNC:31037]","synonyms":"MCT13","biotype":"protein_coding","ncbi_id":"201232","summary":null,"start":7036075,"end":7040121,"strand":1,"description":"solute carrier family 16 member 13 [Source:HGNC Symbol;Acc:HGNC:31037]"}, {"versioned_ensembl_gene_id":"ENSG00000009413.15","gene_symbol":"REV3L","gene_name":"REV3 like, DNA directed polymerase zeta catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9968]","synonyms":"REV3,POLZ","biotype":"protein_coding","ncbi_id":"5980","summary":"The protein encoded by this gene represents the catalytic subunit of DNA polymerase zeta, which functions in translesion DNA synthesis. The encoded protein can be found in mitochondria, where it protects DNA from damage. Defects in this gene are a cause of Mobius syndrome. [provided by RefSeq, Jan 2017]","start":111299028,"end":111483715,"strand":-1,"description":"REV3 like, DNA directed polymerase zeta catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9968]"}, {"versioned_ensembl_gene_id":"ENSG00000128709.12","gene_symbol":"HOXD9","gene_name":"homeobox D9 [Source:HGNC Symbol;Acc:HGNC:5140]","synonyms":"HOX4C,HOX4","biotype":"protein_coding","ncbi_id":"3235","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The exact role of this gene has not been determined. [provided by RefSeq, Jul 2008]","start":176122720,"end":176124937,"strand":1,"description":"homeobox D9 [Source:HGNC Symbol;Acc:HGNC:5140]"}, {"versioned_ensembl_gene_id":"ENSG00000220392.1","gene_symbol":"FCF1P5","gene_name":"FCF1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479045","summary":null,"start":111353702,"end":111354183,"strand":1,"description":"FCF1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44617]"}, {"versioned_ensembl_gene_id":"ENSG00000169239.12","gene_symbol":"CA5B","gene_name":"carbonic anhydrase 5B [Source:HGNC Symbol;Acc:HGNC:1378]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11238","summary":"Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. This gene encodes carbonic anhydrase 5B. CA5B, and the related CA5A gene, has its expression localized in the mitochondria though CA5B has a wider tissue distribution than CA5A, which is restricted to the liver, kidneys, and skeletal muscle. A carbonic anhydrase pseudogene (CA5BP1) is adjacent to the CA5B gene and these two loci produce CA5BP1-CA5B readthrough transcripts. [provided by RefSeq, Jan 2019]","start":15688830,"end":15788409,"strand":1,"description":"carbonic anhydrase 5B [Source:HGNC Symbol;Acc:HGNC:1378]"}, {"versioned_ensembl_gene_id":"ENSG00000279949.1","gene_symbol":"AC022784.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9158063,"end":9158621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253426.5","gene_symbol":"AC022784.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9151742,"end":9168136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282411.1","gene_symbol":"AC233699.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36274563,"end":36320919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134086.7","gene_symbol":"VHL","gene_name":"von Hippel-Lindau tumor suppressor [Source:HGNC Symbol;Acc:HGNC:12687]","synonyms":"VHL1","biotype":"protein_coding","ncbi_id":"7428","summary":"Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. A germline mutation of this gene is the basis of familial inheritance of VHL syndrome. The protein encoded by this gene is a component of the protein complex that includes elongin B, elongin C, and cullin-2, and possesses ubiquitin ligase E3 activity. This protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen. RNA polymerase II subunit POLR2G/RPB7 is also reported to be a target of this protein. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":10141008,"end":10152220,"strand":1,"description":"von Hippel-Lindau tumor suppressor [Source:HGNC Symbol;Acc:HGNC:12687]"}, {"versioned_ensembl_gene_id":"ENSG00000162753.11","gene_symbol":"SLC9C2","gene_name":"solute carrier family 9 member C2 (putative) [Source:HGNC Symbol;Acc:HGNC:28664]","synonyms":"SLC9A11,MGC43026","biotype":"protein_coding","ncbi_id":"284525","summary":null,"start":173500464,"end":173603094,"strand":-1,"description":"solute carrier family 9 member C2 (putative) [Source:HGNC Symbol;Acc:HGNC:28664]"}, {"versioned_ensembl_gene_id":"ENSG00000232113.2","gene_symbol":"TEX50","gene_name":"testis expressed 50 [Source:HGNC Symbol;Acc:HGNC:52382]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730159","summary":null,"start":173635333,"end":173637134,"strand":1,"description":"testis expressed 50 [Source:HGNC Symbol;Acc:HGNC:52382]"}, {"versioned_ensembl_gene_id":"ENSG00000214671.4","gene_symbol":"AC096741.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169166272,"end":169167117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178562.17","gene_symbol":"CD28","gene_name":"CD28 molecule [Source:HGNC Symbol;Acc:HGNC:1653]","synonyms":null,"biotype":"protein_coding","ncbi_id":"940","summary":"The protein encoded by this gene is essential for T-cell proliferation and survival, cytokine production, and T-helper type-2 development. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]","start":203706475,"end":203738912,"strand":1,"description":"CD28 molecule [Source:HGNC Symbol;Acc:HGNC:1653]"}, {"versioned_ensembl_gene_id":"ENSG00000117592.8","gene_symbol":"PRDX6","gene_name":"peroxiredoxin 6 [Source:HGNC Symbol;Acc:HGNC:16753]","synonyms":"PRX,p29,NSGPx,MGC46173,KIAA0106,AOP2,aiPLA2,1-Cys","biotype":"protein_coding","ncbi_id":"9588","summary":"The protein encoded by this gene is a member of the thiol-specific antioxidant protein family. This protein is a bifunctional enzyme with two distinct active sites. It is involved in redox regulation of the cell; it can reduce H(2)O(2) and short chain organic, fatty acid, and phospholipid hydroperoxides. It may play a role in the regulation of phospholipid turnover as well as in protection against oxidative injury. [provided by RefSeq, Jul 2008]","start":173477266,"end":173488807,"strand":1,"description":"peroxiredoxin 6 [Source:HGNC Symbol;Acc:HGNC:16753]"}, {"versioned_ensembl_gene_id":"ENSG00000228719.1","gene_symbol":"AL022313.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36445395,"end":36454944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089250.18","gene_symbol":"NOS1","gene_name":"nitric oxide synthase 1 [Source:HGNC Symbol;Acc:HGNC:7872]","synonyms":"NOS,nNOS","biotype":"protein_coding","ncbi_id":"4842","summary":"The protein encoded by this gene belongs to the family of nitric oxide synthases, which synthesize nitric oxide from L-arginine. Nitric oxide is a reactive free radical, which acts as a biologic mediator in several processes, including neurotransmission, and antimicrobial and antitumoral activities. In the brain and peripheral nervous system, nitric oxide displays many properties of a neurotransmitter, and has been implicated in neurotoxicity associated with stroke and neurodegenerative diseases, neural regulation of smooth muscle, including peristalsis, and penile erection. This protein is ubiquitously expressed, with high level of expression in skeletal muscle. Multiple transcript variants that differ in the 5' UTR have been described for this gene but the full-length nature of these transcripts is not known. Additionally, alternatively spliced transcript variants encoding different isoforms (some testis-specific) have been found for this gene.[provided by RefSeq, Feb 2011]","start":117208142,"end":117452170,"strand":-1,"description":"nitric oxide synthase 1 [Source:HGNC Symbol;Acc:HGNC:7872]"}, {"versioned_ensembl_gene_id":"ENSG00000215328.6","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31805699,"end":31808181,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000283580.1","gene_symbol":"AC098484.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42767292,"end":42794493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135914.5","gene_symbol":"HTR2B","gene_name":"5-hydroxytryptamine receptor 2B [Source:HGNC Symbol;Acc:HGNC:5294]","synonyms":"5-HT2B,5-HT(2B)","biotype":"protein_coding","ncbi_id":"3357","summary":"This gene encodes one of the several different receptors for 5-hydroxytryptamine (serotonin) that belongs to the G-protein coupled receptor 1 family. Serotonin is a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. Serotonin receptors mediate many of the central and peripheral physiologic functions of serotonin, including regulation of cardiovascular functions and impulsive behavior. Population and family-based analyses of a minor allele (glutamine-to-stop substitution, designated Q20*) which blocks expression of this protein, and knockout studies in mice, suggest a role for this gene in impulsivity. However, other factors, such as elevated testosterone levels, may also be involved. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]","start":231108230,"end":231125118,"strand":-1,"description":"5-hydroxytryptamine receptor 2B [Source:HGNC Symbol;Acc:HGNC:5294]"}, {"versioned_ensembl_gene_id":"ENSG00000254177.1","gene_symbol":"AC079209.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81058523,"end":81067744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159251.6","gene_symbol":"ACTC1","gene_name":"actin, alpha, cardiac muscle 1 [Source:HGNC Symbol;Acc:HGNC:143]","synonyms":"CMD1R,ACTC","biotype":"protein_coding","ncbi_id":"70","summary":"Actins are highly conserved proteins that are involved in various types of cell motility. Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to four others. The protein encoded by this gene belongs to the actin family which is comprised of three main groups of actin isoforms, alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. Defects in this gene have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC). [provided by RefSeq, Jul 2008]","start":34788096,"end":34796139,"strand":-1,"description":"actin, alpha, cardiac muscle 1 [Source:HGNC Symbol;Acc:HGNC:143]"}, {"versioned_ensembl_gene_id":"ENSG00000273654.1","gene_symbol":"AC020904.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18022403,"end":18032099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235903.7","gene_symbol":"CPB2-AS1","gene_name":"CPB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39898]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100509894","summary":null,"start":46052806,"end":46113332,"strand":1,"description":"CPB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39898]"}, {"versioned_ensembl_gene_id":"ENSG00000180992.6","gene_symbol":"MRPL14","gene_name":"mitochondrial ribosomal protein L14 [Source:HGNC Symbol;Acc:HGNC:14279]","synonyms":"RPML32,MRP-L32","biotype":"protein_coding","ncbi_id":"64928","summary":"This nuclear gene encodes a protein component of the 39S subunit of the mitochondrial ribosome. A pseudogene of this gene is found on chromosome 17. [provided by RefSeq, Jan 2016]","start":44113454,"end":44127457,"strand":-1,"description":"mitochondrial ribosomal protein L14 [Source:HGNC Symbol;Acc:HGNC:14279]"}, {"versioned_ensembl_gene_id":"ENSG00000148950.9","gene_symbol":"IMMP1L","gene_name":"inner mitochondrial membrane peptidase subunit 1 [Source:HGNC Symbol;Acc:HGNC:26317]","synonyms":"IMMP1,FLJ25059","biotype":"protein_coding","ncbi_id":"196294","summary":"The mitochondrial inner membrane peptidase (IMP) complex generates mature, active proteins in the mitochondrial intermembrane space by proteolytically removing the mitochondrial targeting presequence of nuclear-encoded proteins. IMP1 and IMP2 (IMMP2L; MIM 605977) are the catalytic subunits of the IMP complex (Burri et al., 2005 [PubMed 15814844]).[supplied by OMIM, Sep 2008]","start":31432401,"end":31509645,"strand":-1,"description":"inner mitochondrial membrane peptidase subunit 1 [Source:HGNC Symbol;Acc:HGNC:26317]"}, {"versioned_ensembl_gene_id":"ENSG00000278602.1","gene_symbol":"AC006338.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24977176,"end":24978317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276726.4","gene_symbol":"DNAJA3","gene_name":"DnaJ heat shock protein family (Hsp40) member A3 [Source:HGNC Symbol;Acc:HGNC:11808]","synonyms":"TID1,hTid-1","biotype":"protein_coding","ncbi_id":"9093","summary":"This gene encodes a member of the DNAJ/Hsp40 protein family. DNAJ/Hsp40 proteins stimulate the ATPase activity of Hsp70 chaperones and play critical roles in protein folding, degradation, and multimeric complex assembly. The encoded protein is localized to mitochondria and mediates several cellular processes including proliferation, survival and apoptotic signal transduction. The encoded protein also plays a critical role in tumor suppression through interactions with oncogenic proteins including ErbB2 and the p53 tumor suppressor protein. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":4427764,"end":4458734,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A3 [Source:HGNC Symbol;Acc:HGNC:11808]"}, {"versioned_ensembl_gene_id":"ENSG00000001461.16","gene_symbol":"NIPAL3","gene_name":"NIPA like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25233]","synonyms":"NPAL3,DJ462O23.2","biotype":"protein_coding","ncbi_id":"57185","summary":null,"start":24415794,"end":24472976,"strand":1,"description":"NIPA like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25233]"}, {"versioned_ensembl_gene_id":"ENSG00000211776.2","gene_symbol":"TRAV2","gene_name":"T-cell receptor alpha variable 2 [Source:HGNC Symbol;Acc:HGNC:12116]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28691","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21712321,"end":21712843,"strand":1,"description":"T-cell receptor alpha variable 2 [Source:HGNC Symbol;Acc:HGNC:12116]"}, {"versioned_ensembl_gene_id":"ENSG00000228358.5","gene_symbol":"LINC02263","gene_name":"long intergenic non-protein coding RNA 2263 [Source:HGNC Symbol;Acc:HGNC:53175]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377390","summary":null,"start":117360625,"end":117372852,"strand":1,"description":"long intergenic non-protein coding RNA 2263 [Source:HGNC Symbol;Acc:HGNC:53175]"}, {"versioned_ensembl_gene_id":"ENSG00000124003.12","gene_symbol":"MOGAT1","gene_name":"monoacylglycerol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:18210]","synonyms":"DGAT2L,MGAT1,DGAT2L1","biotype":"protein_coding","ncbi_id":"116255","summary":"Acyl-CoA:monoacylglycerol acyltransferase (MOGAT; EC 2.3.1.22) catalyzes the synthesis of diacylglycerols, the precursor of physiologically important lipids such as triacylglycerol and phospholipids (Yen et al., 2002 [PubMed 12077311]).[supplied by OMIM, Mar 2008]","start":222671786,"end":222709930,"strand":1,"description":"monoacylglycerol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:18210]"}, {"versioned_ensembl_gene_id":"ENSG00000117122.13","gene_symbol":"MFAP2","gene_name":"microfibril associated protein 2 [Source:HGNC Symbol;Acc:HGNC:7033]","synonyms":"MAGP-1,MAGP","biotype":"protein_coding","ncbi_id":"4237","summary":"Microfibrillar-associated protein 2 is a major antigen of elastin-associated microfibrils and a candidate for involvement in the etiology of inherited connective tissue diseases. Four transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":16974502,"end":16980835,"strand":-1,"description":"microfibril associated protein 2 [Source:HGNC Symbol;Acc:HGNC:7033]"}, {"versioned_ensembl_gene_id":"ENSG00000230701.2","gene_symbol":"FBXW4P1","gene_name":"F-box and WD repeat domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13609]","synonyms":"SHFM3P1,FBXW3,FBW3","biotype":"processed_pseudogene","ncbi_id":"26226","summary":null,"start":23262767,"end":23265005,"strand":1,"description":"F-box and WD repeat domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13609]"}, {"versioned_ensembl_gene_id":"ENSG00000273628.1","gene_symbol":"AL354798.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24933006,"end":24936796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177138.15","gene_symbol":"FAM9B","gene_name":"family with sequence similarity 9 member B [Source:HGNC Symbol;Acc:HGNC:18404]","synonyms":"TEX39B","biotype":"protein_coding","ncbi_id":"171483","summary":"This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex protein. [provided by RefSeq, Aug 2011]","start":9024232,"end":9164639,"strand":-1,"description":"family with sequence similarity 9 member B [Source:HGNC Symbol;Acc:HGNC:18404]"}, {"versioned_ensembl_gene_id":"ENSG00000230849.2","gene_symbol":"GOT2P2","gene_name":"glutamic-oxaloacetic transaminase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4435]","synonyms":"GOT2L2","biotype":"processed_pseudogene","ncbi_id":"391139","summary":null,"start":173141100,"end":173142350,"strand":-1,"description":"glutamic-oxaloacetic transaminase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4435]"}, {"versioned_ensembl_gene_id":"ENSG00000282826.1","gene_symbol":"FRG1CP","gene_name":"FSHD region gene 1 family member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:51762]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100289097","summary":null,"start":28580709,"end":28602664,"strand":-1,"description":"FSHD region gene 1 family member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:51762]"}, {"versioned_ensembl_gene_id":"ENSG00000159363.17","gene_symbol":"ATP13A2","gene_name":"ATPase 13A2 [Source:HGNC Symbol;Acc:HGNC:30213]","synonyms":"PARK9,HSA9947,CLN12","biotype":"protein_coding","ncbi_id":"23400","summary":"This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]","start":16985958,"end":17011928,"strand":-1,"description":"ATPase 13A2 [Source:HGNC Symbol;Acc:HGNC:30213]"}, {"versioned_ensembl_gene_id":"ENSG00000160679.12","gene_symbol":"CHTOP","gene_name":"chromatin target of PRMT1 [Source:HGNC Symbol;Acc:HGNC:24511]","synonyms":"SRAG,FOP,DKFZP547E1010,C1orf77","biotype":"protein_coding","ncbi_id":"26097","summary":"This gene encodes a small nuclear protein that is characterized by an arginine and glycine rich region. This protein may have an important role in the regulation of fetal globin gene expression and in the activation of estrogen-responsive genes. A recent study reported that this protein binds 5-hydroxymethylcytosine (5hmC) and associates with an arginine methyltransferase complex (methylosome), which promotes methylation of arginine 3 of histone H4 (H4R3) and activation of genes involved in glioblastomagenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Nov 2015]","start":153633982,"end":153646306,"strand":1,"description":"chromatin target of PRMT1 [Source:HGNC Symbol;Acc:HGNC:24511]"}, {"versioned_ensembl_gene_id":"ENSG00000138138.13","gene_symbol":"ATAD1","gene_name":"ATPase family, AAA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25903]","synonyms":"FLJ14600","biotype":"protein_coding","ncbi_id":"84896","summary":null,"start":87751512,"end":87841343,"strand":-1,"description":"ATPase family, AAA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25903]"}, {"versioned_ensembl_gene_id":"ENSG00000250627.2","gene_symbol":"TTC39CP1","gene_name":"tetratricopeptide repeat domain 39C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44019]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288825","summary":null,"start":116193997,"end":116194751,"strand":-1,"description":"tetratricopeptide repeat domain 39C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44019]"}, {"versioned_ensembl_gene_id":"ENSG00000215790.6","gene_symbol":"SLC35E2","gene_name":"solute carrier family 35 member E2 [Source:HGNC Symbol;Acc:HGNC:20863]","synonyms":"KIAA0447","biotype":"protein_coding","ncbi_id":"9906","summary":null,"start":1724838,"end":1745992,"strand":-1,"description":"solute carrier family 35 member E2 [Source:HGNC Symbol;Acc:HGNC:20863]"}, {"versioned_ensembl_gene_id":"ENSG00000162302.12","gene_symbol":"RPS6KA4","gene_name":"ribosomal protein S6 kinase A4 [Source:HGNC Symbol;Acc:HGNC:10433]","synonyms":"RSK-B,MSK2","biotype":"protein_coding","ncbi_id":"8986","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 non-identical kinase catalytic domains and phosphorylates various substrates, including CREB1 and ATF1. The encoded protein can also phosphorylate histone H3 to regulate certain inflammatory genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":64359148,"end":64372215,"strand":1,"description":"ribosomal protein S6 kinase A4 [Source:HGNC Symbol;Acc:HGNC:10433]"}, {"versioned_ensembl_gene_id":"ENSG00000241511.1","gene_symbol":"AC026979.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30117384,"end":30117779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224637.1","gene_symbol":"PDSS1P2","gene_name":"decaprenyl diphosphate synthase subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49741]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996500","summary":null,"start":44166266,"end":44166943,"strand":1,"description":"decaprenyl diphosphate synthase subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49741]"}, {"versioned_ensembl_gene_id":"ENSG00000281081.1","gene_symbol":"AC114936.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177944158,"end":177987099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219391.1","gene_symbol":"AC019129.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44065894,"end":44066154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244444.6","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"NG3,C6orf8","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32122191,"end":32125889,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000240935.6","gene_symbol":"PLGLA","gene_name":"plasminogen-like A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9074]","synonyms":"PLGP2,PLGLA1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285189","summary":null,"start":106382171,"end":106393031,"strand":1,"description":"plasminogen-like A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9074]"}, {"versioned_ensembl_gene_id":"ENSG00000101193.7","gene_symbol":"GID8","gene_name":"GID complex subunit 8 homolog [Source:HGNC Symbol;Acc:HGNC:15857]","synonyms":"TWA1,FLJ20602,C20orf11,bA305P22.1","biotype":"protein_coding","ncbi_id":"54994","summary":null,"start":62938119,"end":62948475,"strand":1,"description":"GID complex subunit 8 homolog [Source:HGNC Symbol;Acc:HGNC:15857]"}, {"versioned_ensembl_gene_id":"ENSG00000205777.17","gene_symbol":"GAGE1","gene_name":"G antigen 1 [Source:HGNC Symbol;Acc:HGNC:4098]","synonyms":"CT4.1","biotype":"protein_coding","ncbi_id":"2543","summary":"This gene belongs to a family of genes that are expressed in a variety of tumors but not in normal tissues, except for the testis. The sequences of the family members are highly related but differ by scattered nucleotide substitutions. The antigenic peptide YRPRPRRY, which is also encoded by several other family members, is recognized by autologous cytolytic T lymphocytes. Nothing is presently known about the function of this protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":49589496,"end":49608536,"strand":1,"description":"G antigen 1 [Source:HGNC Symbol;Acc:HGNC:4098]"}, {"versioned_ensembl_gene_id":"ENSG00000225390.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31734608,"end":31737000,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000169075.7","gene_symbol":"Z99496.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118501430,"end":118502906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248572.5","gene_symbol":"EGFLAM-AS2","gene_name":"EGFLAM antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41168]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506475","summary":null,"start":38399814,"end":38403413,"strand":-1,"description":"EGFLAM antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41168]"}, {"versioned_ensembl_gene_id":"ENSG00000232533.1","gene_symbol":"AC093673.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143379692,"end":143380495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261829.1","gene_symbol":"AC009407.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":231052040,"end":231052637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233939.1","gene_symbol":"AC114755.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106304755,"end":106305197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104369.4","gene_symbol":"JPH1","gene_name":"junctophilin 1 [Source:HGNC Symbol;Acc:HGNC:14201]","synonyms":"JP-1","biotype":"protein_coding","ncbi_id":"56704","summary":"Junctional complexes between the plasma membrane and endoplasmic/sarcoplasmic reticulum are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. The protein encoded by this gene is a component of junctional complexes and is composed of a C-terminal hydrophobic segment spanning the endoplasmic/sarcoplasmic reticulum membrane and a remaining cytoplasmic domain that shows specific affinity for the plasma membrane. This gene is a member of the junctophilin gene family. [provided by RefSeq, Jul 2008]","start":74234700,"end":74321328,"strand":-1,"description":"junctophilin 1 [Source:HGNC Symbol;Acc:HGNC:14201]"}, {"versioned_ensembl_gene_id":"ENSG00000278731.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"CD158B1,nkat6,CD158k,cl-43","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754673,"end":54769220,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000275434.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54459987,"end":54474463,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000224061.1","gene_symbol":"AC092106.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106253231,"end":106253717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272619.1","gene_symbol":"AC093673.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143363899,"end":143364229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260782.1","gene_symbol":"AC007225.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46789898,"end":46792040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276501.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54861074,"end":54875379,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000254772.9","gene_symbol":"EEF1G","gene_name":"eukaryotic translation elongation factor 1 gamma [Source:HGNC Symbol;Acc:HGNC:3213]","synonyms":"EF1G","biotype":"protein_coding","ncbi_id":"1937","summary":"This gene encodes a subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This subunit contains an N-terminal glutathione transferase domain, which may be involved in regulating the assembly of multisubunit complexes containing this elongation factor and aminoacyl-tRNA synthetases. [provided by RefSeq, Jul 2008]","start":62559601,"end":62574086,"strand":-1,"description":"eukaryotic translation elongation factor 1 gamma [Source:HGNC Symbol;Acc:HGNC:3213]"}, {"versioned_ensembl_gene_id":"ENSG00000274324.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877320,"end":54892899,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000235750.9","gene_symbol":"KIAA0040","gene_name":"KIAA0040 [Source:HGNC Symbol;Acc:HGNC:28950]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9674","summary":null,"start":175156987,"end":175192999,"strand":-1,"description":"KIAA0040 [Source:HGNC Symbol;Acc:HGNC:28950]"}, {"versioned_ensembl_gene_id":"ENSG00000215156.5","gene_symbol":"AC138409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34190056,"end":34193653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174579.3","gene_symbol":"MSL2","gene_name":"MSL complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:25544]","synonyms":"RNF184,MSL2L1,KIAA1585,msl-2,FLJ10546","biotype":"protein_coding","ncbi_id":"55167","summary":null,"start":136148922,"end":136197241,"strand":-1,"description":"MSL complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:25544]"}, {"versioned_ensembl_gene_id":"ENSG00000241438.1","gene_symbol":"TDGF1P6","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:11706]","synonyms":"TDGF6,CRIPTO-6,CR-6","biotype":"processed_pseudogene","ncbi_id":"22813","summary":null,"start":136155549,"end":136155996,"strand":1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:11706]"}, {"versioned_ensembl_gene_id":"ENSG00000198682.12","gene_symbol":"PAPSS2","gene_name":"3'-phosphoadenosine 5'-phosphosulfate synthase 2 [Source:HGNC Symbol;Acc:HGNC:8604]","synonyms":"ATPSK2","biotype":"protein_coding","ncbi_id":"9060","summary":"Sulfation is a common modification of endogenous (lipids, proteins, and carbohydrates) and exogenous (xenobiotics and drugs) compounds. In mammals, the sulfate source is 3'-phosphoadenosine 5'-phosphosulfate (PAPS), created from ATP and inorganic sulfate. Two different tissue isoforms encoded by different genes synthesize PAPS. This gene encodes one of the two PAPS synthetases. Defects in this gene cause the Pakistani type of spondyloepimetaphyseal dysplasia. Two alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":87659613,"end":87747705,"strand":1,"description":"3'-phosphoadenosine 5'-phosphosulfate synthase 2 [Source:HGNC Symbol;Acc:HGNC:8604]"}, {"versioned_ensembl_gene_id":"ENSG00000262573.2","gene_symbol":"KRTAP9-2","gene_name":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]","synonyms":"KAP9.2","biotype":"protein_coding","ncbi_id":"83899","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41226627,"end":41227631,"strand":1,"description":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]"}, {"versioned_ensembl_gene_id":"ENSG00000262120.1","gene_symbol":"AC010547.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71420483,"end":71421518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237295.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32332954,"end":32333913,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000262946.1","gene_symbol":"KRTAP9-11P","gene_name":"keratin associated protein 9-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18918]","synonyms":"KRTAP9P1,KAP9A","biotype":"unprocessed_pseudogene","ncbi_id":"85347","summary":null,"start":41259941,"end":41260465,"strand":1,"description":"keratin associated protein 9-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18918]"}, {"versioned_ensembl_gene_id":"ENSG00000214062.5","gene_symbol":"RPL7P17","gene_name":"ribosomal protein L7 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270851","summary":null,"start":77082403,"end":77083126,"strand":-1,"description":"ribosomal protein L7 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36116]"}, {"versioned_ensembl_gene_id":"ENSG00000251590.1","gene_symbol":"NIFKP7","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44955]","synonyms":"MKI67IPP7","biotype":"unprocessed_pseudogene","ncbi_id":"106479049","summary":null,"start":32063974,"end":32066611,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44955]"}, {"versioned_ensembl_gene_id":"ENSG00000280532.1","gene_symbol":"AL732314.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":421847,"end":424670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091536.16","gene_symbol":"MYO15A","gene_name":"myosin XVA [Source:HGNC Symbol;Acc:HGNC:7594]","synonyms":"MYO15,DFNB3","biotype":"protein_coding","ncbi_id":"51168","summary":"This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]","start":18108706,"end":18179802,"strand":1,"description":"myosin XVA [Source:HGNC Symbol;Acc:HGNC:7594]"}, {"versioned_ensembl_gene_id":"ENSG00000206102.2","gene_symbol":"KRTAP19-8","gene_name":"keratin associated protein 19-8 [Source:HGNC Symbol;Acc:HGNC:33898]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728299","summary":null,"start":31038159,"end":31038476,"strand":-1,"description":"keratin associated protein 19-8 [Source:HGNC Symbol;Acc:HGNC:33898]"}, {"versioned_ensembl_gene_id":"ENSG00000259906.1","gene_symbol":"AC120045.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30170563,"end":30179943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102901.12","gene_symbol":"CENPT","gene_name":"centromere protein T [Source:HGNC Symbol;Acc:HGNC:25787]","synonyms":"FLJ13111,CENP-T,C16orf56","biotype":"protein_coding","ncbi_id":"80152","summary":"The centromere is a specialized chromatin domain, present throughout the cell cycle, that acts as a platform on which the transient assembly of the kinetochore occurs during mitosis. All active centromeres are characterized by the presence of long arrays of nucleosomes in which CENPA (MIM 117139) replaces histone H3 (see MIM 601128). CENPT is an additional factor required for centromere assembly (Foltz et al., 2006 [PubMed 16622419]).[supplied by OMIM, Mar 2008]","start":67828157,"end":67847811,"strand":-1,"description":"centromere protein T [Source:HGNC Symbol;Acc:HGNC:25787]"}, {"versioned_ensembl_gene_id":"ENSG00000099991.17","gene_symbol":"CABIN1","gene_name":"calcineurin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24187]","synonyms":"PPP3IN,KIAA0330","biotype":"protein_coding","ncbi_id":"23523","summary":"Calcineurin plays an important role in the T-cell receptor-mediated signal transduction pathway. The protein encoded by this gene binds specifically to the activated form of calcineurin and inhibits calcineurin-mediated signal transduction. The encoded protein is found in the nucleus and contains a leucine zipper domain as well as several PEST motifs, sequences which confer targeted degradation to those proteins which contain them. Alternative splicing results in multiple transcript variants encoding two different isoforms. [provided by RefSeq, Jan 2011]","start":24011192,"end":24178628,"strand":1,"description":"calcineurin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24187]"}, {"versioned_ensembl_gene_id":"ENSG00000274093.1","gene_symbol":"AC009032.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":69632141,"end":69632571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272554.1","gene_symbol":"AC012087.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24496272,"end":24499580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269978.1","gene_symbol":"AL359881.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7700704,"end":7700970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233544.1","gene_symbol":"EIF3KP2","gene_name":"eukaryotic translation initiation factor 3 subunit K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129045","summary":null,"start":24555834,"end":24556459,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44017]"}, {"versioned_ensembl_gene_id":"ENSG00000232786.1","gene_symbol":"TIMM9P3","gene_name":"TIMM9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862725","summary":null,"start":45552863,"end":45553136,"strand":-1,"description":"TIMM9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39930]"}, {"versioned_ensembl_gene_id":"ENSG00000225489.6","gene_symbol":"AL354707.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6716495,"end":6727438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166225.8","gene_symbol":"FRS2","gene_name":"fibroblast growth factor receptor substrate 2 [Source:HGNC Symbol;Acc:HGNC:16971]","synonyms":"SNT1,SNT-1,FRS2alpha,FRS2A","biotype":"protein_coding","ncbi_id":"10818","summary":null,"start":69470349,"end":69579789,"strand":1,"description":"fibroblast growth factor receptor substrate 2 [Source:HGNC Symbol;Acc:HGNC:16971]"}, {"versioned_ensembl_gene_id":"ENSG00000165837.11","gene_symbol":"ERICH6B","gene_name":"glutamate rich 6B [Source:HGNC Symbol;Acc:HGNC:26523]","synonyms":"FLJ32682,FAM194B","biotype":"protein_coding","ncbi_id":"220081","summary":null,"start":45534522,"end":45615739,"strand":-1,"description":"glutamate rich 6B [Source:HGNC Symbol;Acc:HGNC:26523]"}, {"versioned_ensembl_gene_id":"ENSG00000227805.1","gene_symbol":"RPL21P90","gene_name":"ribosomal protein L21 pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:35548]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271423","summary":null,"start":95999778,"end":96000243,"strand":-1,"description":"ribosomal protein L21 pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:35548]"}, {"versioned_ensembl_gene_id":"ENSG00000227254.1","gene_symbol":"VDAC1P12","gene_name":"voltage dependent anion channel 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39680]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874289","summary":null,"start":34082429,"end":34083310,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39680]"}, {"versioned_ensembl_gene_id":"ENSG00000253699.1","gene_symbol":"AC084128.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86180418,"end":86212236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280310.1","gene_symbol":"AC092437.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4820405,"end":4821452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278973.1","gene_symbol":"AC073592.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124622290,"end":124623069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275911.3","gene_symbol":"NDE1","gene_name":"nudE neurodevelopment protein 1 [Source:HGNC Symbol;Acc:HGNC:17619]","synonyms":"NDE,FLJ20101,nudE","biotype":"protein_coding","ncbi_id":"54820","summary":"This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":15728421,"end":15811507,"strand":1,"description":"nudE neurodevelopment protein 1 [Source:HGNC Symbol;Acc:HGNC:17619]"}, {"versioned_ensembl_gene_id":"ENSG00000254981.1","gene_symbol":"AC087623.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38400536,"end":38401683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279536.1","gene_symbol":"AC093458.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":149881477,"end":149882105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232946.1","gene_symbol":"AL354707.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6675284,"end":6675614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282330.1","gene_symbol":"AC068473.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79683041,"end":79685112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250741.6","gene_symbol":"NT5C1B-RDH14","gene_name":"NT5C1B-RDH14 readthrough [Source:HGNC Symbol;Acc:HGNC:38831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526794","summary":"This locus represents naturally occurring read-through transcription between the neighboring NT5C1B (5'-nucleotidase, cytosolic IB) and RDH14 (retinol dehydrogenase 14) genes on chromosome 2. Alternative splicing results in multiple transcript variants, one of which encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]","start":18555545,"end":18589564,"strand":-1,"description":"NT5C1B-RDH14 readthrough [Source:HGNC Symbol;Acc:HGNC:38831]"}, {"versioned_ensembl_gene_id":"ENSG00000236857.3","gene_symbol":"RAP1BP1","gene_name":"RAP1B, member of RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506390","summary":null,"start":18717974,"end":18718526,"strand":-1,"description":"RAP1B, member of RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49780]"}, {"versioned_ensembl_gene_id":"ENSG00000232048.2","gene_symbol":"HNRNPCP9","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48820]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130196","summary":null,"start":67660155,"end":67661013,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48820]"}, {"versioned_ensembl_gene_id":"ENSG00000234127.8","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30184455,"end":30213427,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000243195.1","gene_symbol":"TUBBP11","gene_name":"tubulin beta class I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42184]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480745","summary":null,"start":103630661,"end":103630912,"strand":1,"description":"tubulin beta class I pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42184]"}, {"versioned_ensembl_gene_id":"ENSG00000220212.1","gene_symbol":"OR4F1P","gene_name":"olfactory receptor family 4 subfamily F member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8298]","synonyms":"OR4F1,HSDJ0609N19","biotype":"unprocessed_pseudogene","ncbi_id":"26685","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":105919,"end":106856,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8298]"}, {"versioned_ensembl_gene_id":"ENSG00000262521.1","gene_symbol":"AJ003147.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3181233,"end":3184018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272384.1","gene_symbol":"AC016405.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122779971,"end":122780830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232976.1","gene_symbol":"TRIM60P10Y","gene_name":"tripartite motif containing 60 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:38462]","synonyms":"TRIM60PY10,TRIM60P10","biotype":"processed_pseudogene","ncbi_id":"100420376","summary":null,"start":24659337,"end":24660406,"strand":1,"description":"tripartite motif containing 60 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:38462]"}, {"versioned_ensembl_gene_id":"ENSG00000235726.5","gene_symbol":"AC010148.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":234834315,"end":234913384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122477.12","gene_symbol":"LRRC39","gene_name":"leucine rich repeat containing 39 [Source:HGNC Symbol;Acc:HGNC:28228]","synonyms":"MGC14816","biotype":"protein_coding","ncbi_id":"127495","summary":null,"start":100148449,"end":100178273,"strand":-1,"description":"leucine rich repeat containing 39 [Source:HGNC Symbol;Acc:HGNC:28228]"}, {"versioned_ensembl_gene_id":"ENSG00000234842.1","gene_symbol":"MTCO2P16","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52032]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075148","summary":null,"start":201549631,"end":201550307,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52032]"}, {"versioned_ensembl_gene_id":"ENSG00000275363.1","gene_symbol":"AC100757.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22451209,"end":22455154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256750.1","gene_symbol":"LINC02423","gene_name":"long intergenic non-protein coding RNA 2423 [Source:HGNC Symbol;Acc:HGNC:53353]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370014","summary":null,"start":118758754,"end":118761679,"strand":-1,"description":"long intergenic non-protein coding RNA 2423 [Source:HGNC Symbol;Acc:HGNC:53353]"}, {"versioned_ensembl_gene_id":"ENSG00000174444.14","gene_symbol":"RPL4","gene_name":"ribosomal protein L4 [Source:HGNC Symbol;Acc:HGNC:10353]","synonyms":"L4","biotype":"protein_coding","ncbi_id":"6124","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L4E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":66498015,"end":66524532,"strand":-1,"description":"ribosomal protein L4 [Source:HGNC Symbol;Acc:HGNC:10353]"}, {"versioned_ensembl_gene_id":"ENSG00000250583.1","gene_symbol":"AC034232.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33519616,"end":33522230,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241746.1","gene_symbol":"AC104212.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80265528,"end":80266155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237949.1","gene_symbol":"LINC00844","gene_name":"long intergenic non-protein coding RNA 844 [Source:HGNC Symbol;Acc:HGNC:45031]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507008","summary":null,"start":58999626,"end":59001543,"strand":1,"description":"long intergenic non-protein coding RNA 844 [Source:HGNC Symbol;Acc:HGNC:45031]"}, {"versioned_ensembl_gene_id":"ENSG00000241590.1","gene_symbol":"RPL17P37","gene_name":"ribosomal protein L17 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36854]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271411","summary":null,"start":118737964,"end":118738511,"strand":-1,"description":"ribosomal protein L17 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36854]"}, {"versioned_ensembl_gene_id":"ENSG00000229116.2","gene_symbol":"AL137026.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44282926,"end":44293709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241346.1","gene_symbol":"SNRPCP11","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310850","summary":null,"start":125816082,"end":125816286,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49826]"}, {"versioned_ensembl_gene_id":"ENSG00000273272.1","gene_symbol":"U62317.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50542650,"end":50543011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248787.1","gene_symbol":"AC092903.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125908005,"end":125910272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234799.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30341338,"end":30341472,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000100228.12","gene_symbol":"RAB36","gene_name":"RAB36, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9775]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9609","summary":null,"start":23145326,"end":23164350,"strand":1,"description":"RAB36, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9775]"}, {"versioned_ensembl_gene_id":"ENSG00000261663.1","gene_symbol":"AC009065.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2240487,"end":2241818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239978.1","gene_symbol":"AF186996.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125734295,"end":125735198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270222.1","gene_symbol":"DUXAP11","gene_name":"double homeobox A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51812]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481741","summary":null,"start":59655602,"end":59656336,"strand":1,"description":"double homeobox A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51812]"}, {"versioned_ensembl_gene_id":"ENSG00000230768.7","gene_symbol":"LINC01676","gene_name":"long intergenic non-protein coding RNA 1676 [Source:HGNC Symbol;Acc:HGNC:52464]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928476","summary":null,"start":105587575,"end":105618958,"strand":-1,"description":"long intergenic non-protein coding RNA 1676 [Source:HGNC Symbol;Acc:HGNC:52464]"}, {"versioned_ensembl_gene_id":"ENSG00000279612.1","gene_symbol":"AC231988.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67457499,"end":67458554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262090.1","gene_symbol":"AC136944.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33495943,"end":33496093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225036.1","gene_symbol":"CDK4P1","gene_name":"cyclin dependent kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19040]","synonyms":"CDK4PS","biotype":"processed_pseudogene","ncbi_id":"359941","summary":null,"start":105433994,"end":105434821,"strand":1,"description":"cyclin dependent kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19040]"}, {"versioned_ensembl_gene_id":"ENSG00000261509.6","gene_symbol":"TP53TG3B","gene_name":"TP53 target 3B [Source:HGNC Symbol;Acc:HGNC:37202]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729355","summary":null,"start":33360274,"end":33363478,"strand":1,"description":"TP53 target 3B [Source:HGNC Symbol;Acc:HGNC:37202]"}, {"versioned_ensembl_gene_id":"ENSG00000268209.1","gene_symbol":"AC114786.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69387580,"end":69388307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238062.5","gene_symbol":"SPATA3-AS1","gene_name":"SPATA3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28013]","synonyms":null,"biotype":"lincRNA","ncbi_id":"348761","summary":null,"start":230984368,"end":230996032,"strand":-1,"description":"SPATA3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28013]"}, {"versioned_ensembl_gene_id":"ENSG00000163918.10","gene_symbol":"RFC4","gene_name":"replication factor C subunit 4 [Source:HGNC Symbol;Acc:HGNC:9972]","synonyms":"RFC37,A1","biotype":"protein_coding","ncbi_id":"5984","summary":"The elongation of primed DNA templates by DNA polymerase delta and DNA polymerase epsilon requires the accessory proteins proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). RFC, also named activator 1, is a protein complex consisting of five distinct subunits of 140, 40, 38, 37, and 36 kD. This gene encodes the 37 kD subunit. This subunit forms a core complex with the 36 and 40 kDa subunits. The core complex possesses DNA-dependent ATPase activity, which was found to be stimulated by PCNA in an in vitro system. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":186789880,"end":186807058,"strand":-1,"description":"replication factor C subunit 4 [Source:HGNC Symbol;Acc:HGNC:9972]"}, {"versioned_ensembl_gene_id":"ENSG00000119231.10","gene_symbol":"SENP5","gene_name":"SUMO1/sentrin specific peptidase 5 [Source:HGNC Symbol;Acc:HGNC:28407]","synonyms":"MGC27076","biotype":"protein_coding","ncbi_id":"205564","summary":"The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1; MIM 601912) is required for numerous biologic processes. SUMO-specific proteases, such as SENP5, are responsible for the initial processing of SUMO precursors to generate a C-terminal diglycine motif required for the conjugation reaction. They also have isopeptidase activity for the removal of SUMO from high molecular mass SUMO conjugates (Di Bacco et al., 2006 [PubMed 16738315]).[supplied by OMIM, Jun 2009]","start":196867856,"end":196934714,"strand":1,"description":"SUMO1/sentrin specific peptidase 5 [Source:HGNC Symbol;Acc:HGNC:28407]"}, {"versioned_ensembl_gene_id":"ENSG00000276529.1","gene_symbol":"AP001505.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44978832,"end":44979274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260827.1","gene_symbol":"AC138869.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33203773,"end":33206462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261507.1","gene_symbol":"AC141257.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33206431,"end":33330342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226701.1","gene_symbol":"RPL15P14","gene_name":"ribosomal protein L15 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271283","summary":null,"start":72189941,"end":72190576,"strand":1,"description":"ribosomal protein L15 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36487]"}, {"versioned_ensembl_gene_id":"ENSG00000230565.1","gene_symbol":"ZNF32-AS2","gene_name":"ZNF32 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:23593]","synonyms":"ZNF32OS2,b402L1.7","biotype":"antisense_RNA","ncbi_id":"414208","summary":null,"start":43645942,"end":43648019,"strand":1,"description":"ZNF32 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:23593]"}, {"versioned_ensembl_gene_id":"ENSG00000223398.1","gene_symbol":"AC027124.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13460424,"end":13460889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163755.8","gene_symbol":"HPS3","gene_name":"HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 [Source:HGNC Symbol;Acc:HGNC:15597]","synonyms":"SUTAL,BLOC2S1","biotype":"protein_coding","ncbi_id":"84343","summary":"This gene encodes a protein containing a potential clathrin-binding motif, consensus dileucine signals, and tyrosine-based sorting signals for targeting to vesicles of lysosomal lineage. The encoded protein may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 3. [provided by RefSeq, Apr 2015]","start":149129584,"end":149173732,"strand":1,"description":"HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 [Source:HGNC Symbol;Acc:HGNC:15597]"}, {"versioned_ensembl_gene_id":"ENSG00000238263.1","gene_symbol":"RPL21P88","gene_name":"ribosomal protein L21 pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:35714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271421","summary":null,"start":43630947,"end":43631382,"strand":1,"description":"ribosomal protein L21 pseudogene 88 [Source:HGNC Symbol;Acc:HGNC:35714]"}, {"versioned_ensembl_gene_id":"ENSG00000259647.1","gene_symbol":"AC111152.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30005443,"end":30045848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142864.14","gene_symbol":"SERBP1","gene_name":"SERPINE1 mRNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17860]","synonyms":"PAIRBP1,PAI-RBP1,HABP4L,DKFZP564M2423,CHD3IP,CGI-55","biotype":"protein_coding","ncbi_id":"26135","summary":null,"start":67407810,"end":67430415,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17860]"}, {"versioned_ensembl_gene_id":"ENSG00000226245.1","gene_symbol":"ZNF32-AS1","gene_name":"ZNF32 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23577]","synonyms":"ZNF32OS1,bA402L1.8","biotype":"antisense_RNA","ncbi_id":"414197","summary":null,"start":43643872,"end":43645047,"strand":1,"description":"ZNF32 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23577]"}, {"versioned_ensembl_gene_id":"ENSG00000166510.13","gene_symbol":"CCDC68","gene_name":"coiled-coil domain containing 68 [Source:HGNC Symbol;Acc:HGNC:24350]","synonyms":"SE57-1","biotype":"protein_coding","ncbi_id":"80323","summary":null,"start":54901509,"end":54959508,"strand":-1,"description":"coiled-coil domain containing 68 [Source:HGNC Symbol;Acc:HGNC:24350]"}, {"versioned_ensembl_gene_id":"ENSG00000232973.11","gene_symbol":"CYP1B1-AS1","gene_name":"CYP1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28543]","synonyms":"MGC34824,C2orf58","biotype":"antisense_RNA","ncbi_id":"285154","summary":null,"start":38073447,"end":38231651,"strand":1,"description":"CYP1B1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28543]"}, {"versioned_ensembl_gene_id":"ENSG00000129422.14","gene_symbol":"MTUS1","gene_name":"microtubule associated scaffold protein 1 [Source:HGNC Symbol;Acc:HGNC:29789]","synonyms":"MTSG1,MP44,KIAA1288,ICIS,FLJ14295,DKFZp586D1519,ATIP3,ATIP1,ATBP","biotype":"protein_coding","ncbi_id":"57509","summary":"This gene encodes a protein which contains a C-terminal domain able to interact with the angiotension II (AT2) receptor and a large coiled-coil region allowing dimerization. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. One of the transcript variants has been shown to encode a mitochondrial protein that acts as a tumor suppressor and partcipates in AT2 signaling pathways. Other variants may encode nuclear or transmembrane proteins but it has not been determined whether they also participate in AT2 signaling pathways. [provided by RefSeq, Jul 2008]","start":17643795,"end":17800917,"strand":-1,"description":"microtubule associated scaffold protein 1 [Source:HGNC Symbol;Acc:HGNC:29789]"}, {"versioned_ensembl_gene_id":"ENSG00000224785.1","gene_symbol":"AC006026.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23562459,"end":23564261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266446.1","gene_symbol":"AL449423.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21995482,"end":21996013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138385.15","gene_symbol":"SSB","gene_name":"Sjogren syndrome antigen B [Source:HGNC Symbol;Acc:HGNC:11316]","synonyms":"LARP3,La/SSB,La","biotype":"protein_coding","ncbi_id":"6741","summary":"The protein encoded by this gene is involved in diverse aspects of RNA metabolism, including binding and protecting poly(U) termini of nascent RNA polymerase III transcripts from exonuclease digestion, processing 5' and 3' ends of pre-tRNA precursors, acting as an RNA chaperone, and binding viral RNAs associated with hepatitis C virus. Autoantibodies reacting with this protein are found in the sera of patients with Sjogren syndrome and systemic lupus erythematosus. Alternative promoter usage results in two different transcript variants which encode the same protein. [provided by RefSeq, Jun 2014]","start":169791933,"end":169812064,"strand":1,"description":"Sjogren syndrome antigen B [Source:HGNC Symbol;Acc:HGNC:11316]"}, {"versioned_ensembl_gene_id":"ENSG00000274002.1","gene_symbol":"AL135999.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23619201,"end":23620012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090382.6","gene_symbol":"LYZ","gene_name":"lysozyme [Source:HGNC Symbol;Acc:HGNC:6740]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4069","summary":"This gene encodes human lysozyme, whose natural substrate is the bacterial cell wall peptidoglycan (cleaving the beta[1-4]glycosidic linkages between N-acetylmuramic acid and N-acetylglucosamine). Lysozyme is one of the antimicrobial agents found in human milk, and is also present in spleen, lung, kidney, white blood cells, plasma, saliva, and tears. The protein has antibacterial activity against a number of bacterial species. Missense mutations in this gene have been identified in heritable renal amyloidosis. [provided by RefSeq, Oct 2014]","start":69348341,"end":69354234,"strand":1,"description":"lysozyme [Source:HGNC Symbol;Acc:HGNC:6740]"}, {"versioned_ensembl_gene_id":"ENSG00000138758.11","gene_symbol":"SEPT11","gene_name":"septin 11 [Source:HGNC Symbol;Acc:HGNC:25589]","synonyms":"FLJ10849","biotype":"protein_coding","ncbi_id":"55752","summary":"SEPT11 belongs to the conserved septin family of filament-forming cytoskeletal GTPases that are involved in a variety of cellular functions including cytokinesis and vesicle trafficking (Hanai et al., 2004 [PubMed 15196925]; Nagata et al., 2004 [PubMed 15485874]).[supplied by OMIM, Jul 2009]","start":76949703,"end":77040384,"strand":1,"description":"septin 11 [Source:HGNC Symbol;Acc:HGNC:25589]"}, {"versioned_ensembl_gene_id":"ENSG00000271288.1","gene_symbol":"IGHV1OR15-3","gene_name":"immunoglobulin heavy variable 1/OR15-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5565]","synonyms":"IGHV1/OR15-3","biotype":"IG_V_pseudogene","ncbi_id":"646370","summary":null,"start":22178107,"end":22178542,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5565]"}, {"versioned_ensembl_gene_id":"ENSG00000277654.5","gene_symbol":"AC087633.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":94841059,"end":95169864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260419.1","gene_symbol":"AC138869.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33191561,"end":33195354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149633.11","gene_symbol":"KIAA1755","gene_name":"KIAA1755 [Source:HGNC Symbol;Acc:HGNC:29372]","synonyms":"RP5-1054A22.3","biotype":"protein_coding","ncbi_id":"85449","summary":null,"start":38210488,"end":38260772,"strand":-1,"description":"KIAA1755 [Source:HGNC Symbol;Acc:HGNC:29372]"}, {"versioned_ensembl_gene_id":"ENSG00000231776.5","gene_symbol":"LINC01611","gene_name":"long intergenic non-protein coding RNA 1611 [Source:HGNC Symbol;Acc:HGNC:51791]","synonyms":"TCONS_l2_00025430,RP1-90L14.1","biotype":"lincRNA","ncbi_id":"105377880","summary":null,"start":84421028,"end":84556152,"strand":-1,"description":"long intergenic non-protein coding RNA 1611 [Source:HGNC Symbol;Acc:HGNC:51791]"}, {"versioned_ensembl_gene_id":"ENSG00000156136.9","gene_symbol":"DCK","gene_name":"deoxycytidine kinase [Source:HGNC Symbol;Acc:HGNC:2704]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1633","summary":" Deoxycytidine kinase (DCK) is required for the phosphorylation of several deoxyribonucleosides and their nucleoside analogs. Deficiency of DCK is associated with resistance to antiviral and anticancer chemotherapeutic agents. Conversely, increased deoxycytidine kinase activity is associated with increased activation of these compounds to cytotoxic nucleoside triphosphate derivatives. DCK is clinically important because of its relationship to drug resistance and sensitivity. [provided by RefSeq, Jul 2008]","start":70992538,"end":71030914,"strand":1,"description":"deoxycytidine kinase [Source:HGNC Symbol;Acc:HGNC:2704]"}, {"versioned_ensembl_gene_id":"ENSG00000273661.5","gene_symbol":"AL133414.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54754679,"end":54769001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253833.1","gene_symbol":"AC022868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73984493,"end":73984883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177600.8","gene_symbol":"RPLP2","gene_name":"ribosomal protein lateral stalk subunit P2 [Source:HGNC Symbol;Acc:HGNC:10377]","synonyms":"LP2,D11S2243E,RPP2,P2,MGC71408","biotype":"protein_coding","ncbi_id":"6181","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P1. The P2 protein can interact with P0 and P1 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":809647,"end":812880,"strand":1,"description":"ribosomal protein lateral stalk subunit P2 [Source:HGNC Symbol;Acc:HGNC:10377]"}, {"versioned_ensembl_gene_id":"ENSG00000110799.13","gene_symbol":"VWF","gene_name":"von Willebrand factor [Source:HGNC Symbol;Acc:HGNC:12726]","synonyms":"F8VWF","biotype":"protein_coding","ncbi_id":"7450","summary":"This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]","start":5948874,"end":6124770,"strand":-1,"description":"von Willebrand factor [Source:HGNC Symbol;Acc:HGNC:12726]"}, {"versioned_ensembl_gene_id":"ENSG00000263103.1","gene_symbol":"KRTAP9-10P","gene_name":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480422","summary":null,"start":41270282,"end":41270488,"strand":1,"description":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]"}, {"versioned_ensembl_gene_id":"ENSG00000224439.2","gene_symbol":"RPSAP10","gene_name":"ribosomal protein SA pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31460]","synonyms":"LAMR1P10","biotype":"processed_pseudogene","ncbi_id":"401638","summary":null,"start":28436201,"end":28437078,"strand":1,"description":"ribosomal protein SA pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:31460]"}, {"versioned_ensembl_gene_id":"ENSG00000184571.13","gene_symbol":"PIWIL3","gene_name":"piwi like RNA-mediated gene silencing 3 [Source:HGNC Symbol;Acc:HGNC:18443]","synonyms":"HIWI3","biotype":"protein_coding","ncbi_id":"440822","summary":"This gene encodes a member of the PIWI subfamily of Argonaute family proteins. This subfamily of proteins contains a PAZ domain, found in proteins involved in RNA-mediated gene silencing, and a C-terminal Piwi domain. The encoded protein is thought to function in maintenance of germline cells. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":24719034,"end":24774720,"strand":-1,"description":"piwi like RNA-mediated gene silencing 3 [Source:HGNC Symbol;Acc:HGNC:18443]"}, {"versioned_ensembl_gene_id":"ENSG00000132026.13","gene_symbol":"RTBDN","gene_name":"retbindin [Source:HGNC Symbol;Acc:HGNC:30310]","synonyms":"FLJ36353","biotype":"protein_coding","ncbi_id":"83546","summary":"This gene was first identified in a study of human eye tissues. The protein encoded by this gene is preferentially expressed in the retina and may play a role in binding retinoids and other carotenoids as it shares homology with riboflavin binding proteins. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":12825478,"end":12835428,"strand":-1,"description":"retbindin [Source:HGNC Symbol;Acc:HGNC:30310]"}, {"versioned_ensembl_gene_id":"ENSG00000054118.13","gene_symbol":"THRAP3","gene_name":"thyroid hormone receptor associated protein 3 [Source:HGNC Symbol;Acc:HGNC:22964]","synonyms":"TRAP150,BCLAF2","biotype":"protein_coding","ncbi_id":"9967","summary":null,"start":36224416,"end":36305357,"strand":1,"description":"thyroid hormone receptor associated protein 3 [Source:HGNC Symbol;Acc:HGNC:22964]"}, {"versioned_ensembl_gene_id":"ENSG00000254709.7","gene_symbol":"IGLL5","gene_name":"immunoglobulin lambda like polypeptide 5 [Source:HGNC Symbol;Acc:HGNC:38476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100423062","summary":"This gene encodes one of the immunoglobulin lambda-like polypeptides. It is located within the immunoglobulin lambda locus but it does not require somatic rearrangement for expression. The first exon of this gene is unrelated to immunoglobulin variable genes; the second and third exons are the immunoglobulin lambda joining 1 and the immunoglobulin lambda constant 1 gene segments. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":22887780,"end":22896107,"strand":1,"description":"immunoglobulin lambda like polypeptide 5 [Source:HGNC Symbol;Acc:HGNC:38476]"}, {"versioned_ensembl_gene_id":"ENSG00000215288.4","gene_symbol":"AC067904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27011147,"end":27012371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263232.2","gene_symbol":"ATP5A1P3","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:829]","synonyms":"ATP5AP3","biotype":"processed_pseudogene","ncbi_id":"645443","summary":null,"start":72005037,"end":72006543,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:829]"}, {"versioned_ensembl_gene_id":"ENSG00000241053.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30224316,"end":30316381,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000277273.5","gene_symbol":"CDK7","gene_name":"cyclin dependent kinase 7 [Source:HGNC Symbol;Acc:HGNC:1778]","synonyms":"CDKN7,CAK1,CAK,STK1,MO15","biotype":"protein_coding","ncbi_id":"1022","summary":"The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of Saccharomyces cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, and are known to be important regulators of cell cycle progression. This protein forms a trimeric complex with cyclin H and MAT1, which functions as a Cdk-activating kinase (CAK). It is an essential component of the transcription factor TFIIH, that is involved in transcription initiation and DNA repair. This protein is thought to serve as a direct link between the regulation of transcription and the cell cycle. [provided by RefSeq, Jul 2008]","start":69234793,"end":69277413,"strand":1,"description":"cyclin dependent kinase 7 [Source:HGNC Symbol;Acc:HGNC:1778]"}, {"versioned_ensembl_gene_id":"ENSG00000253234.1","gene_symbol":"IGLV2-5","gene_name":"immunoglobulin lambda variable 2-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5894]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28818","summary":null,"start":22856762,"end":22857038,"strand":1,"description":"immunoglobulin lambda variable 2-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5894]"}, {"versioned_ensembl_gene_id":"ENSG00000266286.2","gene_symbol":"AC037482.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41084386,"end":41085542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101444.12","gene_symbol":"AHCY","gene_name":"adenosylhomocysteinase [Source:HGNC Symbol;Acc:HGNC:343]","synonyms":"SAHH","biotype":"protein_coding","ncbi_id":"191","summary":"S-adenosylhomocysteine hydrolase belongs to the adenosylhomocysteinase family. It catalyzes the reversible hydrolysis of S-adenosylhomocysteine (AdoHcy) to adenosine (Ado) and L-homocysteine (Hcy). Thus, it regulates the intracellular S-adenosylhomocysteine (SAH) concentration thought to be important for transmethylation reactions. Deficiency in this protein is one of the different causes of hypermethioninemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":34280268,"end":34311802,"strand":-1,"description":"adenosylhomocysteinase [Source:HGNC Symbol;Acc:HGNC:343]"}, {"versioned_ensembl_gene_id":"ENSG00000174840.8","gene_symbol":"PDE12","gene_name":"phosphodiesterase 12 [Source:HGNC Symbol;Acc:HGNC:25386]","synonyms":"DKFZp667B1218,2'-PDE","biotype":"protein_coding","ncbi_id":"201626","summary":null,"start":57556276,"end":57566844,"strand":1,"description":"phosphodiesterase 12 [Source:HGNC Symbol;Acc:HGNC:25386]"}, {"versioned_ensembl_gene_id":"ENSG00000185088.13","gene_symbol":"RPS27L","gene_name":"ribosomal protein S27 like [Source:HGNC Symbol;Acc:HGNC:18476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51065","summary":"This gene encodes a protein sharing 96% amino acid similarity with ribosomal protein S27, which suggests the encoded protein may be a component of the 40S ribosomal subunit. [provided by RefSeq, Jul 2008]","start":63125872,"end":63158021,"strand":-1,"description":"ribosomal protein S27 like [Source:HGNC Symbol;Acc:HGNC:18476]"}, {"versioned_ensembl_gene_id":"ENSG00000273567.1","gene_symbol":"REXO1L3P","gene_name":"REXO1 like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32240]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441359","summary":null,"start":85654684,"end":85658514,"strand":-1,"description":"REXO1 like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32240]"}, {"versioned_ensembl_gene_id":"ENSG00000244429.1","gene_symbol":"AC104629.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166293756,"end":166294353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240084.1","gene_symbol":"MTND4LP10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42244]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075099","summary":null,"start":166160414,"end":166160704,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42244]"}, {"versioned_ensembl_gene_id":"ENSG00000211664.3","gene_symbol":"IGLV2-18","gene_name":"immunoglobulin lambda variable 2-18 [Source:HGNC Symbol;Acc:HGNC:5889]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28814","summary":null,"start":22734607,"end":22735089,"strand":1,"description":"immunoglobulin lambda variable 2-18 [Source:HGNC Symbol;Acc:HGNC:5889]"}, {"versioned_ensembl_gene_id":"ENSG00000225491.1","gene_symbol":"UBE2Q2P4Y","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38429]","synonyms":"UBE2Q2PY1","biotype":"unprocessed_pseudogene","ncbi_id":"100421716","summary":null,"start":24232826,"end":24238984,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38429]"}, {"versioned_ensembl_gene_id":"ENSG00000250455.1","gene_symbol":"AC117532.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37377049,"end":37377971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224816.1","gene_symbol":"NAP1L4P2","gene_name":"nucleosome assembly protein 1 like 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874319","summary":null,"start":106466542,"end":106467440,"strand":-1,"description":"nucleosome assembly protein 1 like 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39739]"}, {"versioned_ensembl_gene_id":"ENSG00000272836.1","gene_symbol":"AL022328.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50205585,"end":50206062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226277.1","gene_symbol":"AC105393.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":421057,"end":422303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256713.7","gene_symbol":"PGA5","gene_name":"pepsinogen 5, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8887]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5222","summary":"This gene encodes a protein precursor of the digestive enzyme pepsin, a member of the peptidase A1 family of endopeptidases. The encoded precursor is secreted by gastric chief cells and undergoes autocatalytic cleavage in acidic conditions to form the active enzyme, which functions in the digestion of dietary proteins. This gene is found in a cluster of related genes on chromosome 11, each of which encodes one of multiple pepsinogens. Pepsinogen levels in serum may serve as a biomarker for atrophic gastritis and gastric cancer. [provided by RefSeq, Jul 2015]","start":61241042,"end":61251448,"strand":1,"description":"pepsinogen 5, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8887]"}, {"versioned_ensembl_gene_id":"ENSG00000221962.5","gene_symbol":"TMEM14EP","gene_name":"transmembrane protein 14E, pseudogene [Source:HGNC Symbol;Acc:HGNC:34386]","synonyms":"TMEM14E","biotype":"transcribed_processed_pseudogene","ncbi_id":"645843","summary":null,"start":152339695,"end":152340990,"strand":-1,"description":"transmembrane protein 14E, pseudogene [Source:HGNC Symbol;Acc:HGNC:34386]"}, {"versioned_ensembl_gene_id":"ENSG00000170185.9","gene_symbol":"USP38","gene_name":"ubiquitin specific peptidase 38 [Source:HGNC Symbol;Acc:HGNC:20067]","synonyms":"KIAA1891,HP43.8KD","biotype":"protein_coding","ncbi_id":"84640","summary":null,"start":143184917,"end":143223830,"strand":1,"description":"ubiquitin specific peptidase 38 [Source:HGNC Symbol;Acc:HGNC:20067]"}, {"versioned_ensembl_gene_id":"ENSG00000229183.8","gene_symbol":"PGA4","gene_name":"pepsinogen 4, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8886]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643847","summary":"This gene encodes a protein precursor of the digestive enzyme pepsin, a member of the peptidase A1 family of endopeptidases. The encoded precursor is secreted by gastric chief cells and undergoes autocatalytic cleavage in acidic conditions to form the active enzyme, which functions in the digestion of dietary proteins. This gene is found in a cluster of related genes on chromosome 11, each of which encodes one of multiple pepsinogens. Pepsinogen levels in serum may serve as a biomarker for atrophic gastritis and gastric cancer. [provided by RefSeq, Jul 2015]","start":61222216,"end":61231927,"strand":1,"description":"pepsinogen 4, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8886]"}, {"versioned_ensembl_gene_id":"ENSG00000224105.2","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31189747,"end":31191083,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000267811.1","gene_symbol":"AP001160.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62771120,"end":62771606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177822.7","gene_symbol":"AC098864.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181874438,"end":182145249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271130.1","gene_symbol":"IGHV3OR16-8","gene_name":"immunoglobulin heavy variable 3/OR16-8 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5643]","synonyms":"IGHV3/OR16-8","biotype":"IG_V_gene","ncbi_id":"388255","summary":null,"start":33009175,"end":33009620,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-8 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5643]"}, {"versioned_ensembl_gene_id":"ENSG00000180385.8","gene_symbol":"EMC3-AS1","gene_name":"EMC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49223]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442075","summary":null,"start":9986893,"end":10006990,"strand":1,"description":"EMC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49223]"}, {"versioned_ensembl_gene_id":"ENSG00000134333.13","gene_symbol":"LDHA","gene_name":"lactate dehydrogenase A [Source:HGNC Symbol;Acc:HGNC:6535]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3939","summary":"The protein encoded by this gene catalyzes the conversion of L-lactate and NAD to pyruvate and NADH in the final step of anaerobic glycolysis. The protein is found predominantly in muscle tissue and belongs to the lactate dehydrogenase family. Mutations in this gene have been linked to exertional myoglobinuria. Multiple transcript variants encoding different isoforms have been found for this gene. The human genome contains several non-transcribed pseudogenes of this gene. [provided by RefSeq, Sep 2008]","start":18394388,"end":18408425,"strand":1,"description":"lactate dehydrogenase A [Source:HGNC Symbol;Acc:HGNC:6535]"}, {"versioned_ensembl_gene_id":"ENSG00000251297.1","gene_symbol":"TUBB7P","gene_name":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]","synonyms":"TUBB4Q","biotype":"unprocessed_pseudogene","ncbi_id":"56604","summary":null,"start":189982523,"end":189984871,"strand":-1,"description":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]"}, {"versioned_ensembl_gene_id":"ENSG00000224807.5","gene_symbol":"DUX4L9","gene_name":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288711","summary":null,"start":190021407,"end":190022665,"strand":-1,"description":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]"}, {"versioned_ensembl_gene_id":"ENSG00000257232.1","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"C6orf37,bCX105N19.6,PBLT","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":31019512,"end":31029672,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000242156.1","gene_symbol":"AC000041.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29419155,"end":29423193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230526.1","gene_symbol":"AC073370.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71878356,"end":71879107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228448.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"processed_transcript","ncbi_id":"102723346","summary":null,"start":31024520,"end":31024900,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000248770.1","gene_symbol":"AC019235.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":181237358,"end":181237564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258570.1","gene_symbol":"AC110027.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94168349,"end":94168751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249460.1","gene_symbol":"LINC02500","gene_name":"long intergenic non-protein coding RNA 2500 [Source:HGNC Symbol;Acc:HGNC:53488]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928679","summary":null,"start":181261161,"end":181265029,"strand":-1,"description":"long intergenic non-protein coding RNA 2500 [Source:HGNC Symbol;Acc:HGNC:53488]"}, {"versioned_ensembl_gene_id":"ENSG00000205097.6","gene_symbol":"FRG2","gene_name":"FSHD region gene 2 [Source:HGNC Symbol;Acc:HGNC:19136]","synonyms":"FRG2A","biotype":"protein_coding","ncbi_id":"448831","summary":null,"start":190024351,"end":190027257,"strand":-1,"description":"FSHD region gene 2 [Source:HGNC Symbol;Acc:HGNC:19136]"}, {"versioned_ensembl_gene_id":"ENSG00000100280.16","gene_symbol":"AP1B1","gene_name":"adaptor related protein complex 1 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:554]","synonyms":"CLAPB2,BAM22,AP105A,ADTB1","biotype":"protein_coding","ncbi_id":"162","summary":"Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as one of the large subunits of this complex and is a member of the adaptin protein family. This gene is a candidate meningioma gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":29327680,"end":29423179,"strand":-1,"description":"adaptor related protein complex 1 beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:554]"}, {"versioned_ensembl_gene_id":"ENSG00000232901.1","gene_symbol":"CYCSP10","gene_name":"cytochrome c, somatic pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:24384]","synonyms":"HCP10","biotype":"processed_pseudogene","ncbi_id":"360166","summary":null,"start":10000647,"end":10000940,"strand":-1,"description":"cytochrome c, somatic pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:24384]"}, {"versioned_ensembl_gene_id":"ENSG00000186162.10","gene_symbol":"CIDECP","gene_name":"cell death-inducing DFFA-like effector c pseudogene [Source:HGNC Symbol;Acc:HGNC:24230]","synonyms":"CICE","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"152302","summary":null,"start":10014238,"end":10026365,"strand":-1,"description":"cell death-inducing DFFA-like effector c pseudogene [Source:HGNC Symbol;Acc:HGNC:24230]"}, {"versioned_ensembl_gene_id":"ENSG00000089195.14","gene_symbol":"TRMT6","gene_name":"tRNA methyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:20900]","synonyms":"MGC5029,Gcd10p,GCD10,CGI-09","biotype":"protein_coding","ncbi_id":"51605","summary":"This gene encodes a member of the tRNA methyltransferase 6 protein family. A similar protein in yeast is part of a two component methyltransferase, which is involved in the posttranslational modification that produces the modified nucleoside 1-methyladenosine in tRNAs. Modified 1-methyladenosine influences initiator methionine stability and may be involved in the replication of human immunodeficiency virus type 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":5937235,"end":5950558,"strand":-1,"description":"tRNA methyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:20900]"}, {"versioned_ensembl_gene_id":"ENSG00000122863.5","gene_symbol":"CHST3","gene_name":"carbohydrate sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:1971]","synonyms":"C6ST1,C6ST","biotype":"protein_coding","ncbi_id":"9469","summary":"This gene encodes an enzyme which catalyzes the sulfation of chondroitin, a proteoglycan found in the extracellular matrix and most cells which is involved in cell migration and differentiation. Mutations in this gene are associated with spondylepiphyseal dysplasia and humerospinal dysostosis. [provided by RefSeq, Mar 2009]","start":71964365,"end":72013564,"strand":1,"description":"carbohydrate sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:1971]"}, {"versioned_ensembl_gene_id":"ENSG00000162630.5","gene_symbol":"B3GALT2","gene_name":"beta-1,3-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:917]","synonyms":"beta3Gal-T2","biotype":"protein_coding","ncbi_id":"8707","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene encodes a protein that functions in N-linked glycoprotein glycosylation and shows strict donor substrate specificity for UDP-galactose. [provided by RefSeq, Jul 2008]","start":193179045,"end":193186654,"strand":-1,"description":"beta-1,3-galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:917]"}, {"versioned_ensembl_gene_id":"ENSG00000160124.9","gene_symbol":"CCDC58","gene_name":"coiled-coil domain containing 58 [Source:HGNC Symbol;Acc:HGNC:31136]","synonyms":"FLJ33273","biotype":"protein_coding","ncbi_id":"131076","summary":null,"start":122359591,"end":122383231,"strand":-1,"description":"coiled-coil domain containing 58 [Source:HGNC Symbol;Acc:HGNC:31136]"}, {"versioned_ensembl_gene_id":"ENSG00000134028.14","gene_symbol":"ADAMDEC1","gene_name":"ADAM like decysin 1 [Source:HGNC Symbol;Acc:HGNC:16299]","synonyms":"M12.219","biotype":"protein_coding","ncbi_id":"27299","summary":"This encoded protein is thought to be a secreted protein belonging to the disintegrin metalloproteinase family. Its expression is upregulated during dendritic cells maturation. This protein may play an important role in dendritic cell function and their interactions with germinal center T cells. [provided by RefSeq, Jul 2008]","start":24384285,"end":24406013,"strand":1,"description":"ADAM like decysin 1 [Source:HGNC Symbol;Acc:HGNC:16299]"}, {"versioned_ensembl_gene_id":"ENSG00000113407.13","gene_symbol":"TARS","gene_name":"threonyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:11572]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6897","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Threonyl-tRNA synthetase belongs to the class-II aminoacyl-tRNA synthetase family [provided by RefSeq, Jul 2008]","start":33440696,"end":33469539,"strand":1,"description":"threonyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:11572]"}, {"versioned_ensembl_gene_id":"ENSG00000225356.3","gene_symbol":"AC093840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":181522666,"end":181523001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251336.1","gene_symbol":"TEMN3-AS1","gene_name":"TENM3 antisense transcript 1 [Source:HGNC Symbol;Acc:HGNC:53456]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377573","summary":null,"start":181820019,"end":181829973,"strand":-1,"description":"TENM3 antisense transcript 1 [Source:HGNC Symbol;Acc:HGNC:53456]"}, {"versioned_ensembl_gene_id":"ENSG00000168569.7","gene_symbol":"TMEM223","gene_name":"transmembrane protein 223 [Source:HGNC Symbol;Acc:HGNC:28464]","synonyms":"MGC3196","biotype":"protein_coding","ncbi_id":"79064","summary":null,"start":62771629,"end":62792021,"strand":-1,"description":"transmembrane protein 223 [Source:HGNC Symbol;Acc:HGNC:28464]"}, {"versioned_ensembl_gene_id":"ENSG00000272988.1","gene_symbol":"AC022392.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72053294,"end":72054037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259644.1","gene_symbol":"AC022613.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29728186,"end":29729531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274897.2","gene_symbol":"PANO1","gene_name":"proapoptotic nucleolar protein 1 [Source:HGNC Symbol;Acc:HGNC:51237]","synonyms":"PANO","biotype":"protein_coding","ncbi_id":"101927423","summary":null,"start":797511,"end":799190,"strand":1,"description":"proapoptotic nucleolar protein 1 [Source:HGNC Symbol;Acc:HGNC:51237]"}, {"versioned_ensembl_gene_id":"ENSG00000236723.2","gene_symbol":"AL606760.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53209783,"end":53213775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206567.9","gene_symbol":"AC022007.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10006418,"end":10011209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119943.12","gene_symbol":"PYROXD2","gene_name":"pyridine nucleotide-disulphide oxidoreductase domain 2 [Source:HGNC Symbol;Acc:HGNC:23517]","synonyms":"FLJ23849,C10orf33","biotype":"protein_coding","ncbi_id":"84795","summary":null,"start":98383565,"end":98415184,"strand":-1,"description":"pyridine nucleotide-disulphide oxidoreductase domain 2 [Source:HGNC Symbol;Acc:HGNC:23517]"}, {"versioned_ensembl_gene_id":"ENSG00000198356.11","gene_symbol":"ASNA1","gene_name":"arsA arsenite transporter, ATP-binding, homolog 1 (bacterial) [Source:HGNC Symbol;Acc:HGNC:752]","synonyms":"GET3,ARSA-I,TRC40","biotype":"protein_coding","ncbi_id":"439","summary":"This gene represents the human homolog of the bacterial arsA gene, encoding the arsenite-stimulated ATPase component of the arsenite transporter responsible for resistance to arsenicals. This protein is also a central component of a transmembrane domain (TMD) recognition complex (TRC) that is involved in the post-translational delivery of tail-anchored (TA) proteins from the cytosol to the endoplasmic reticulum (ER). It recognizes and selectively binds the TMD of TA proteins in the cytosol, and delivers them to the ER for insertion. [provided by RefSeq, Oct 2011]","start":12737139,"end":12748323,"strand":1,"description":"arsA arsenite transporter, ATP-binding, homolog 1 (bacterial) [Source:HGNC Symbol;Acc:HGNC:752]"}, {"versioned_ensembl_gene_id":"ENSG00000104067.16","gene_symbol":"TJP1","gene_name":"tight junction protein 1 [Source:HGNC Symbol;Acc:HGNC:11827]","synonyms":"ZO-1,MGC133289,DKFZp686M05161,ZO-1,MGC133289,DKFZp686M05161","biotype":"protein_coding","ncbi_id":"7082","summary":"This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family of proteins, and acts as a tight junction adaptor protein that also regulates adherens junctions. Tight junctions regulate the movement of ions and macromolecules between endothelial and epithelial cells. The multidomain structure of this scaffold protein, including a postsynaptic density 95/disc-large/zona occludens (PDZ) domain, a Src homology (SH3) domain, a guanylate kinase (GuK) domain and unique (U) motifs all help to co-ordinate binding of transmembrane proteins, cytosolic proteins, and F-actin, which are required for tight junction function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]","start":29699367,"end":29968865,"strand":-1,"description":"tight junction protein 1 [Source:HGNC Symbol;Acc:HGNC:11827]"}, {"versioned_ensembl_gene_id":"ENSG00000162227.7","gene_symbol":"TAF6L","gene_name":"TATA-box binding protein associated factor 6 like [Source:HGNC Symbol;Acc:HGNC:17305]","synonyms":"PAF65A","biotype":"protein_coding","ncbi_id":"10629","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes a protein that is a component of the PCAF histone acetylase complex and structurally similar to one of the histone-like TAFs, TAF6. The PCAF histone acetylase complex, which is composed of more than 20 polypeptides some of which are TAFs, is required for myogenic transcription and differentiation. [provided by RefSeq, Jul 2008]","start":62771303,"end":62787342,"strand":1,"description":"TATA-box binding protein associated factor 6 like [Source:HGNC Symbol;Acc:HGNC:17305]"}, {"versioned_ensembl_gene_id":"ENSG00000177542.10","gene_symbol":"SLC25A22","gene_name":"solute carrier family 25 member 22 [Source:HGNC Symbol;Acc:HGNC:19954]","synonyms":"EIEE3,NET44,GC1,FLJ13044","biotype":"protein_coding","ncbi_id":"79751","summary":"This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jul 2010]","start":790475,"end":798333,"strand":-1,"description":"solute carrier family 25 member 22 [Source:HGNC Symbol;Acc:HGNC:19954]"}, {"versioned_ensembl_gene_id":"ENSG00000242659.1","gene_symbol":"AC108693.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113746872,"end":113747408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223721.3","gene_symbol":"UQCRFS1P2","gene_name":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39172]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647123","summary":null,"start":138701607,"end":138703062,"strand":1,"description":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39172]"}, {"versioned_ensembl_gene_id":"ENSG00000157184.6","gene_symbol":"CPT2","gene_name":"carnitine palmitoyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:2330]","synonyms":"CPTASE,CPT1","biotype":"protein_coding","ncbi_id":"1376","summary":"The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]","start":53196429,"end":53214197,"strand":1,"description":"carnitine palmitoyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:2330]"}, {"versioned_ensembl_gene_id":"ENSG00000215159.3","gene_symbol":"AC025262.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64759521,"end":64779318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269982.1","gene_symbol":"AC018809.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9958717,"end":9962539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248211.1","gene_symbol":"TRPC7-AS1","gene_name":"TRPC7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40936]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874024","summary":null,"start":136214048,"end":136222159,"strand":1,"description":"TRPC7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40936]"}, {"versioned_ensembl_gene_id":"ENSG00000228598.1","gene_symbol":"MACC1-AS1","gene_name":"MACC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41257]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874041","summary":null,"start":20141916,"end":20153531,"strand":1,"description":"MACC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41257]"}, {"versioned_ensembl_gene_id":"ENSG00000144554.10","gene_symbol":"FANCD2","gene_name":"Fanconi anemia complementation group D2 [Source:HGNC Symbol;Acc:HGNC:3585]","synonyms":"FANCD,FAD,FACD,FA-D2","biotype":"protein_coding","ncbi_id":"2177","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":10026414,"end":10101930,"strand":1,"description":"Fanconi anemia complementation group D2 [Source:HGNC Symbol;Acc:HGNC:3585]"}, {"versioned_ensembl_gene_id":"ENSG00000251433.1","gene_symbol":"CCNHP1","gene_name":"cyclin H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50854]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128118","summary":null,"start":181905790,"end":181906467,"strand":-1,"description":"cyclin H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50854]"}, {"versioned_ensembl_gene_id":"ENSG00000248816.1","gene_symbol":"AC079226.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":182697902,"end":182708042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248266.1","gene_symbol":"AC108142.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":182144852,"end":182190382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218336.8","gene_symbol":"TENM3","gene_name":"teneurin transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:29944]","synonyms":"Ten-M3,ODZ3,KIAA1455","biotype":"protein_coding","ncbi_id":"55714","summary":"This gene encodes a large transmembrane protein that may be involved in the regulation of neuronal development. Mutation in this gene causes microphthalmia. [provided by RefSeq, Aug 2015]","start":182143987,"end":182803024,"strand":1,"description":"teneurin transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:29944]"}, {"versioned_ensembl_gene_id":"ENSG00000227506.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":31062263,"end":31068453,"strand":1,"description":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]"}, {"versioned_ensembl_gene_id":"ENSG00000259852.2","gene_symbol":"IGHV1OR16-2","gene_name":"immunoglobulin heavy variable 1/OR16-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5571]","synonyms":"IGHV1/OR16-2","biotype":"IG_V_pseudogene","ncbi_id":"28314","summary":null,"start":32978461,"end":32978891,"strand":1,"description":"immunoglobulin heavy variable 1/OR16-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5571]"}, {"versioned_ensembl_gene_id":"ENSG00000103042.8","gene_symbol":"SLC38A7","gene_name":"solute carrier family 38 member 7 [Source:HGNC Symbol;Acc:HGNC:25582]","synonyms":"FLJ10815","biotype":"protein_coding","ncbi_id":"55238","summary":null,"start":58665109,"end":58685104,"strand":-1,"description":"solute carrier family 38 member 7 [Source:HGNC Symbol;Acc:HGNC:25582]"}, {"versioned_ensembl_gene_id":"ENSG00000164008.14","gene_symbol":"C1orf50","gene_name":"chromosome 1 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:28795]","synonyms":"MGC955","biotype":"protein_coding","ncbi_id":"79078","summary":null,"start":42767269,"end":42775747,"strand":1,"description":"chromosome 1 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:28795]"}, {"versioned_ensembl_gene_id":"ENSG00000270864.1","gene_symbol":"IGHV3OR16-6","gene_name":"immunoglobulin heavy variable 3/OR16-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5641]","synonyms":"IGHV3/OR16-6","biotype":"IG_V_pseudogene","ncbi_id":"647187","summary":null,"start":32915074,"end":32915536,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5641]"}, {"versioned_ensembl_gene_id":"ENSG00000134463.14","gene_symbol":"ECHDC3","gene_name":"enoyl-CoA hydratase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23489]","synonyms":"FLJ20909","biotype":"protein_coding","ncbi_id":"79746","summary":null,"start":11742366,"end":11764070,"strand":1,"description":"enoyl-CoA hydratase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23489]"}, {"versioned_ensembl_gene_id":"ENSG00000183137.14","gene_symbol":"CEP57L1","gene_name":"centrosomal protein 57 like 1 [Source:HGNC Symbol;Acc:HGNC:21561]","synonyms":"MGC21731,C6orf182,bA487F23.2","biotype":"protein_coding","ncbi_id":"285753","summary":null,"start":109095110,"end":109163932,"strand":1,"description":"centrosomal protein 57 like 1 [Source:HGNC Symbol;Acc:HGNC:21561]"}, {"versioned_ensembl_gene_id":"ENSG00000233732.5","gene_symbol":"IGHV3OR16-10","gene_name":"immunoglobulin heavy variable 3/OR16-10 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5634]","synonyms":"IGHV3/OR16-10","biotype":"IG_V_gene","ncbi_id":"28306","summary":null,"start":32995048,"end":32995505,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-10 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5634]"}, {"versioned_ensembl_gene_id":"ENSG00000228523.1","gene_symbol":"AL389925.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67278052,"end":67278779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259997.2","gene_symbol":"IGHV1OR16-4","gene_name":"immunoglobulin heavy variable 1/OR16-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5573]","synonyms":"IGHV1/OR16-4","biotype":"IG_V_pseudogene","ncbi_id":"28312","summary":null,"start":33002333,"end":33002621,"strand":1,"description":"immunoglobulin heavy variable 1/OR16-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5573]"}, {"versioned_ensembl_gene_id":"ENSG00000261259.1","gene_symbol":"AC142086.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32951993,"end":33028037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280353.1","gene_symbol":"AC011466.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48198107,"end":48199720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271075.1","gene_symbol":"AL139317.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52871458,"end":52872217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236255.1","gene_symbol":"AC009404.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117833937,"end":117841658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280183.1","gene_symbol":"AC067852.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":42598643,"end":42599177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279016.1","gene_symbol":"AC093648.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":148819351,"end":148819956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251418.2","gene_symbol":"ASS1P8","gene_name":"argininosuccinate synthetase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:771]","synonyms":"ASSP8","biotype":"processed_pseudogene","ncbi_id":"453","summary":null,"start":148526493,"end":148527139,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:771]"}, {"versioned_ensembl_gene_id":"ENSG00000250115.2","gene_symbol":"AK3P2","gene_name":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]","synonyms":"HsT26053","biotype":"processed_pseudogene","ncbi_id":"100419074","summary":null,"start":143057060,"end":143057816,"strand":-1,"description":"adenylate kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31099]"}, {"versioned_ensembl_gene_id":"ENSG00000224848.1","gene_symbol":"AL589843.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96687056,"end":96721121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139725.7","gene_symbol":"RHOF","gene_name":"ras homolog family member F, filopodia associated [Source:HGNC Symbol;Acc:HGNC:15703]","synonyms":"RIF,FLJ20247,ARHF","biotype":"protein_coding","ncbi_id":"54509","summary":null,"start":121777754,"end":121803403,"strand":-1,"description":"ras homolog family member F, filopodia associated [Source:HGNC Symbol;Acc:HGNC:15703]"}, {"versioned_ensembl_gene_id":"ENSG00000272849.1","gene_symbol":"AC084018.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121797511,"end":121801972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235584.2","gene_symbol":"AC008268.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95666084,"end":95668715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275395.5","gene_symbol":"FCGBP","gene_name":"Fc fragment of IgG binding protein [Source:HGNC Symbol;Acc:HGNC:13572]","synonyms":"FC(GAMMA)BP,FC(GAMMA)BP","biotype":"protein_coding","ncbi_id":"8857","summary":null,"start":39863323,"end":39934626,"strand":-1,"description":"Fc fragment of IgG binding protein [Source:HGNC Symbol;Acc:HGNC:13572]"}, {"versioned_ensembl_gene_id":"ENSG00000234607.2","gene_symbol":"AL355994.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15969632,"end":15970194,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212694.8","gene_symbol":"LINC01089","gene_name":"long intergenic non-protein coding RNA 1089 [Source:HGNC Symbol;Acc:HGNC:27886]","synonyms":"LIMT","biotype":"lincRNA","ncbi_id":"338799","summary":null,"start":121795267,"end":121803906,"strand":-1,"description":"long intergenic non-protein coding RNA 1089 [Source:HGNC Symbol;Acc:HGNC:27886]"}, {"versioned_ensembl_gene_id":"ENSG00000215198.3","gene_symbol":"AL353795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35147410,"end":35149184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166750.9","gene_symbol":"SLFN5","gene_name":"schlafen family member 5 [Source:HGNC Symbol;Acc:HGNC:28286]","synonyms":"MGC19764","biotype":"protein_coding","ncbi_id":"162394","summary":null,"start":35243036,"end":35273655,"strand":1,"description":"schlafen family member 5 [Source:HGNC Symbol;Acc:HGNC:28286]"}, {"versioned_ensembl_gene_id":"ENSG00000134014.16","gene_symbol":"ELP3","gene_name":"elongator acetyltransferase complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20696]","synonyms":"KAT9,FLJ10422","biotype":"protein_coding","ncbi_id":"55140","summary":"ELP3 is the catalytic subunit of the histone acetyltransferase elongator complex, which contributes to transcript elongation and also regulates the maturation of projection neurons (Creppe et al., 2009 [PubMed 19185337]).[supplied by OMIM, Apr 2009]","start":28089673,"end":28191156,"strand":1,"description":"elongator acetyltransferase complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:20696]"}, {"versioned_ensembl_gene_id":"ENSG00000124702.17","gene_symbol":"KLHDC3","gene_name":"kelch domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20704]","synonyms":"PEAS,hPeas,dJ20C7.3","biotype":"protein_coding","ncbi_id":"116138","summary":"The protein encoded by this gene contains six repeated kelch motifs that are structurally similar to recombination activating gene 2, a protein involved in the activation of the V(D)J recombination. In mouse, this gene is found to be expressed specifically in testis. Its expression in pachytene spermatocytes is localized to cytoplasma and meiotic chromatin, suggesting that this gene may be involved in meiotic recombination. [provided by RefSeq, Jun 2012]","start":43014103,"end":43021298,"strand":1,"description":"kelch domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20704]"}, {"versioned_ensembl_gene_id":"ENSG00000248858.7","gene_symbol":"FLJ46284","gene_name":"uncharacterized LOC441369 [Source:NCBI gene;Acc:441369]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"441369","summary":null,"start":92699742,"end":92879502,"strand":-1,"description":"uncharacterized LOC441369 [Source:NCBI gene;Acc:441369]"}, {"versioned_ensembl_gene_id":"ENSG00000235703.5","gene_symbol":"LINC00894","gene_name":"long intergenic non-protein coding RNA 894 [Source:HGNC Symbol;Acc:HGNC:48579]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100272228","summary":null,"start":149938628,"end":150224580,"strand":1,"description":"long intergenic non-protein coding RNA 894 [Source:HGNC Symbol;Acc:HGNC:48579]"}, {"versioned_ensembl_gene_id":"ENSG00000183171.5","gene_symbol":"BX322650.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150114378,"end":150116520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102383.13","gene_symbol":"ZDHHC15","gene_name":"zinc finger DHHC-type containing 15 [Source:HGNC Symbol;Acc:HGNC:20342]","synonyms":"MRX91,FLJ31812,DHHC15","biotype":"protein_coding","ncbi_id":"158866","summary":"The protein encoded by this gene belongs to the DHHC palmitoyltransferase family. Mutations in this gene are associated with mental retardatio X-linked type 91 (MRX91). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":75368427,"end":75523502,"strand":-1,"description":"zinc finger DHHC-type containing 15 [Source:HGNC Symbol;Acc:HGNC:20342]"}, {"versioned_ensembl_gene_id":"ENSG00000265690.7","gene_symbol":"AC074143.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":67163385,"end":67165815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233254.1","gene_symbol":"RPL21P134","gene_name":"ribosomal protein L21 pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:36006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728782","summary":null,"start":75384346,"end":75384828,"strand":1,"description":"ribosomal protein L21 pseudogene 134 [Source:HGNC Symbol;Acc:HGNC:36006]"}, {"versioned_ensembl_gene_id":"ENSG00000156831.7","gene_symbol":"NSMCE2","gene_name":"NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase [Source:HGNC Symbol;Acc:HGNC:26513]","synonyms":"ZMIZ7,NSE2,MMS21,FLJ32440,C8orf36","biotype":"protein_coding","ncbi_id":"286053","summary":"This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017]","start":125091679,"end":125367120,"strand":1,"description":"NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase [Source:HGNC Symbol;Acc:HGNC:26513]"}, {"versioned_ensembl_gene_id":"ENSG00000266242.1","gene_symbol":"GRAMD4P7","gene_name":"GRAM domain containing 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49142]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631251","summary":null,"start":14485806,"end":14487501,"strand":1,"description":"GRAM domain containing 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49142]"}, {"versioned_ensembl_gene_id":"ENSG00000239675.1","gene_symbol":"CR759835.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28986810,"end":28988546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237921.2","gene_symbol":"AC004543.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19813685,"end":19818090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187554.11","gene_symbol":"TLR5","gene_name":"toll like receptor 5 [Source:HGNC Symbol;Acc:HGNC:11851]","synonyms":"MGC126430,FLJ10052,TIL3,SLEB1,MGC126431","biotype":"protein_coding","ncbi_id":"7100","summary":"This gene encodes a member of the toll-like receptor (TLR) family, which plays a fundamental role in pathogen recognition and activation of innate immune responses. These receptors recognize distinct pathogen-associated molecular patterns that are expressed on infectious agents. The protein encoded by this gene recognizes bacterial flagellin, the principal component of bacterial flagella and a virulence factor. The activation of this receptor mobilizes the nuclear factor NF-kappaB, which in turn activates a host of inflammatory-related target genes. Mutations in this gene have been associated with both resistance and susceptibility to systemic lupus erythematosus, and susceptibility to Legionnaire disease.[provided by RefSeq, Dec 2009]","start":223109406,"end":223143282,"strand":-1,"description":"toll like receptor 5 [Source:HGNC Symbol;Acc:HGNC:11851]"}, {"versioned_ensembl_gene_id":"ENSG00000260401.1","gene_symbol":"AP002761.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":73238975,"end":73242335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121766.15","gene_symbol":"ZCCHC17","gene_name":"zinc finger CCHC-type containing 17 [Source:HGNC Symbol;Acc:HGNC:30246]","synonyms":"pNO40,HSPC251,PS1D","biotype":"protein_coding","ncbi_id":"51538","summary":null,"start":31296982,"end":31364953,"strand":1,"description":"zinc finger CCHC-type containing 17 [Source:HGNC Symbol;Acc:HGNC:30246]"}, {"versioned_ensembl_gene_id":"ENSG00000154001.13","gene_symbol":"PPP2R5E","gene_name":"protein phosphatase 2 regulatory subunit B'epsilon [Source:HGNC Symbol;Acc:HGNC:9313]","synonyms":"B56epsilon,B56E","biotype":"protein_coding","ncbi_id":"5529","summary":"The protein encoded by this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an epsilon isoform of the regulatory subunit B56 subfamily. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":63371357,"end":63543374,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B'epsilon [Source:HGNC Symbol;Acc:HGNC:9313]"}, {"versioned_ensembl_gene_id":"ENSG00000240915.2","gene_symbol":"AC120042.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63013068,"end":63014681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265296.1","gene_symbol":"AP005212.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14391913,"end":14393909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215841.3","gene_symbol":"AP002761.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73214998,"end":73215913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227291.1","gene_symbol":"AC092170.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117180892,"end":117181562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228898.1","gene_symbol":"MTCO1P43","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52108]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075173","summary":null,"start":117026537,"end":117027024,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52108]"}, {"versioned_ensembl_gene_id":"ENSG00000224869.1","gene_symbol":"AC062016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116726453,"end":116726771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103335.21","gene_symbol":"PIEZO1","gene_name":"piezo type mechanosensitive ion channel component 1 [Source:HGNC Symbol;Acc:HGNC:28993]","synonyms":"KIAA0233,FAM38A","biotype":"protein_coding","ncbi_id":"9780","summary":"The protein encoded by this gene is a mechanically-activated ion channel that links mechanical forces to biological signals. The encoded protein contains 36 transmembrane domains and functions as a homotetramer. Defects in this gene have been associated with dehydrated hereditary stomatocytosis. [provided by RefSeq, Jul 2015]","start":88715343,"end":88785211,"strand":-1,"description":"piezo type mechanosensitive ion channel component 1 [Source:HGNC Symbol;Acc:HGNC:28993]"}, {"versioned_ensembl_gene_id":"ENSG00000263535.2","gene_symbol":"AC134669.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31345519,"end":31346190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266371.1","gene_symbol":"AC079915.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31133182,"end":31138518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230301.6","gene_symbol":"OR5H6","gene_name":"olfactory receptor family 5 subfamily H member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14767]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"79295","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":98263252,"end":98265356,"strand":1,"description":"olfactory receptor family 5 subfamily H member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14767]"}, {"versioned_ensembl_gene_id":"ENSG00000187900.4","gene_symbol":"OR5H7P","gene_name":"olfactory receptor family 5 subfamily H member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14771]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79291","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98238352,"end":98239281,"strand":1,"description":"olfactory receptor family 5 subfamily H member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:14771]"}, {"versioned_ensembl_gene_id":"ENSG00000251088.1","gene_symbol":"AC117473.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98233651,"end":98457898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253749.1","gene_symbol":"AC022695.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92420850,"end":92421798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225803.1","gene_symbol":"MRPS11P1","gene_name":"mitochondrial ribosomal protein S11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16584]","synonyms":"dJ746H2.1","biotype":"processed_pseudogene","ncbi_id":"128774","summary":null,"start":20854121,"end":20854642,"strand":-1,"description":"mitochondrial ribosomal protein S11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16584]"}, {"versioned_ensembl_gene_id":"ENSG00000270793.1","gene_symbol":"LLPHP1","gene_name":"LLP homolog, long-term synaptic facilitation pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50491]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480685","summary":null,"start":20721187,"end":20721879,"strand":1,"description":"LLP homolog, long-term synaptic facilitation pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50491]"}, {"versioned_ensembl_gene_id":"ENSG00000137054.15","gene_symbol":"POLR1E","gene_name":"RNA polymerase I subunit E [Source:HGNC Symbol;Acc:HGNC:17631]","synonyms":"PRAF1,PAF53,FLJ13970,FLJ13390","biotype":"protein_coding","ncbi_id":"64425","summary":null,"start":37485935,"end":37503697,"strand":1,"description":"RNA polymerase I subunit E [Source:HGNC Symbol;Acc:HGNC:17631]"}, {"versioned_ensembl_gene_id":"ENSG00000267725.1","gene_symbol":"AC008521.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33067175,"end":33067433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267492.1","gene_symbol":"AL353997.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18453574,"end":18453739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260101.1","gene_symbol":"AC008074.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64522187,"end":64524093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247903.1","gene_symbol":"AC024896.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26971586,"end":26979582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234793.1","gene_symbol":"AC114730.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241754793,"end":241755740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215692.2","gene_symbol":"AC114730.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241734715,"end":241735498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140983.13","gene_symbol":"RHOT2","gene_name":"ras homolog family member T2 [Source:HGNC Symbol;Acc:HGNC:21169]","synonyms":"MIRO-2,C16orf39,ARHT2","biotype":"protein_coding","ncbi_id":"89941","summary":"This gene encodes a member of the Rho family of GTPases. The encoded protein is localized to the outer mitochondrial membrane and plays a role in mitochondrial trafficking and fusion-fission dynamics. [provided by RefSeq, Nov 2011]","start":668086,"end":674174,"strand":1,"description":"ras homolog family member T2 [Source:HGNC Symbol;Acc:HGNC:21169]"}, {"versioned_ensembl_gene_id":"ENSG00000259049.1","gene_symbol":"AL139317.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52775237,"end":52777740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270325.1","gene_symbol":"BNIP3P9","gene_name":"BCL2 interacting protein 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49689]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480280","summary":null,"start":19856975,"end":19857527,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49689]"}, {"versioned_ensembl_gene_id":"ENSG00000035720.7","gene_symbol":"STAP1","gene_name":"signal transducing adaptor family member 1 [Source:HGNC Symbol;Acc:HGNC:24133]","synonyms":"STAP-1,BRDG1","biotype":"protein_coding","ncbi_id":"26228","summary":"The protein encoded by this gene contains a proline-rich region, a pleckstrin homology (PH) domain, and a region in the carboxy terminal half with similarity to the Src Homology 2 (SH2) domain. This protein is a substrate of tyrosine-protein kinase Tec, and its interaction with tyrosine-protein kinase Tec is phosphorylation-dependent. This protein is thought to participate in a positive feedback loop by upregulating the activity of tyrosine-protein kinase Tec. Variants of this gene have been associated with autosomal-dominant hypercholesterolemia (ADH), which is characterized by elevated low-density lipoprotein cholesterol levels and in increased risk of coronary vascular disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":67558728,"end":67607337,"strand":1,"description":"signal transducing adaptor family member 1 [Source:HGNC Symbol;Acc:HGNC:24133]"}, {"versioned_ensembl_gene_id":"ENSG00000145191.12","gene_symbol":"EIF2B5","gene_name":"eukaryotic translation initiation factor 2B subunit epsilon [Source:HGNC Symbol;Acc:HGNC:3261]","synonyms":"EIF2Bepsilon,EIF-2B","biotype":"protein_coding","ncbi_id":"8893","summary":"This gene encodes one of five subunits of eukaryotic translation initiation factor 2B (EIF2B), a GTP exchange factor for eukaryotic initiation factor 2 and an essential regulator for protein synthesis. Mutations in this gene and the genes encoding other EIF2B subunits have been associated with leukoencephalopathy with vanishing white matter. [provided by RefSeq, Nov 2009]","start":184135038,"end":184145311,"strand":1,"description":"eukaryotic translation initiation factor 2B subunit epsilon [Source:HGNC Symbol;Acc:HGNC:3261]"}, {"versioned_ensembl_gene_id":"ENSG00000223917.1","gene_symbol":"AC009237.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95486480,"end":95488627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123584.7","gene_symbol":"MAGEA9","gene_name":"MAGE family member A9 [Source:HGNC Symbol;Acc:HGNC:6807]","synonyms":"MGC8421,MAGE9,CT1.9","biotype":"protein_coding","ncbi_id":"4108","summary":"This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]","start":149781930,"end":149787737,"strand":1,"description":"MAGE family member A9 [Source:HGNC Symbol;Acc:HGNC:6807]"}, {"versioned_ensembl_gene_id":"ENSG00000279762.3","gene_symbol":"AC005899.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32423971,"end":32446038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279713.1","gene_symbol":"AC080038.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":62679403,"end":62681354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272541.1","gene_symbol":"AL021368.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57855891,"end":57856468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245937.7","gene_symbol":"LINC01184","gene_name":"long intergenic non-protein coding RNA 1184 [Source:HGNC Symbol;Acc:HGNC:49565]","synonyms":"FLJ33630","biotype":"lincRNA","ncbi_id":"644873","summary":null,"start":127940426,"end":128083172,"strand":-1,"description":"long intergenic non-protein coding RNA 1184 [Source:HGNC Symbol;Acc:HGNC:49565]"}, {"versioned_ensembl_gene_id":"ENSG00000261039.2","gene_symbol":"LINC02544","gene_name":"long intergenic non-protein coding RNA 2544 [Source:HGNC Symbol;Acc:HGNC:53578]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929504","summary":null,"start":169175304,"end":169182740,"strand":-1,"description":"long intergenic non-protein coding RNA 2544 [Source:HGNC Symbol;Acc:HGNC:53578]"}, {"versioned_ensembl_gene_id":"ENSG00000160712.12","gene_symbol":"IL6R","gene_name":"interleukin 6 receptor [Source:HGNC Symbol;Acc:HGNC:6019]","synonyms":"CD126","biotype":"protein_coding","ncbi_id":"3570","summary":"This gene encodes a subunit of the interleukin 6 (IL6) receptor complex. Interleukin 6 is a potent pleiotropic cytokine that regulates cell growth and differentiation and plays an important role in the immune response. The IL6 receptor is a protein complex consisting of this protein and interleukin 6 signal transducer (IL6ST/GP130/IL6-beta), a receptor subunit also shared by many other cytokines. Dysregulated production of IL6 and this receptor are implicated in the pathogenesis of many diseases, such as multiple myeloma, autoimmune diseases and prostate cancer. Alternatively spliced transcript variants encoding distinct isoforms have been identified in this gene. A pseudogene of this gene is found on chromosome 9. [provided by RefSeq, Aug 2020]","start":154405193,"end":154469450,"strand":1,"description":"interleukin 6 receptor [Source:HGNC Symbol;Acc:HGNC:6019]"}, {"versioned_ensembl_gene_id":"ENSG00000213159.4","gene_symbol":"CEND1P1","gene_name":"cell cycle exit and neuronal differentiation 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43674]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122631","summary":null,"start":104450979,"end":104451433,"strand":1,"description":"cell cycle exit and neuronal differentiation 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43674]"}, {"versioned_ensembl_gene_id":"ENSG00000258598.1","gene_symbol":"AL512357.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104376530,"end":104378951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136874.10","gene_symbol":"STX17","gene_name":"syntaxin 17 [Source:HGNC Symbol;Acc:HGNC:11432]","synonyms":"FLJ20651","biotype":"protein_coding","ncbi_id":"55014","summary":null,"start":99906633,"end":99970341,"strand":1,"description":"syntaxin 17 [Source:HGNC Symbol;Acc:HGNC:11432]"}, {"versioned_ensembl_gene_id":"ENSG00000234281.5","gene_symbol":"LANCL1-AS1","gene_name":"LANCL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50727]","synonyms":"LANCLOT","biotype":"antisense_RNA","ncbi_id":"102724820","summary":null,"start":210324759,"end":210469246,"strand":1,"description":"LANCL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50727]"}, {"versioned_ensembl_gene_id":"ENSG00000254571.1","gene_symbol":"AL358937.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99915077,"end":99929896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114857.17","gene_symbol":"NKTR","gene_name":"natural killer cell triggering receptor [Source:HGNC Symbol;Acc:HGNC:7833]","synonyms":"p104","biotype":"protein_coding","ncbi_id":"4820","summary":"This gene encodes a membrane-anchored protein with a hydrophobic amino terminal domain and a cyclophilin-like PPIase domain. It is present on the surface of natural killer cells and facilitates their binding to targets. Its expression is regulated by IL2 activation of the cells. [provided by RefSeq, Jul 2008]","start":42600614,"end":42648741,"strand":1,"description":"natural killer cell triggering receptor [Source:HGNC Symbol;Acc:HGNC:7833]"}, {"versioned_ensembl_gene_id":"ENSG00000259100.1","gene_symbol":"AL157791.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39385404,"end":39387102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232154.2","gene_symbol":"MTCYBP15","gene_name":"mitochondrially encoded cytochrome b pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:51968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075258","summary":null,"start":237948017,"end":237949143,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:51968]"}, {"versioned_ensembl_gene_id":"ENSG00000248236.1","gene_symbol":"AC008837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99594329,"end":99594740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197882.3","gene_symbol":"OR7E13P","gene_name":"olfactory receptor family 7 subfamily E member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:8384]","synonyms":"OR11-4","biotype":"unprocessed_pseudogene","ncbi_id":"10820","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":86832540,"end":86833449,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:8384]"}, {"versioned_ensembl_gene_id":"ENSG00000269895.1","gene_symbol":"AP000654.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86833068,"end":86837615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186198.3","gene_symbol":"SLC51B","gene_name":"solute carrier family 51 beta subunit [Source:HGNC Symbol;Acc:HGNC:29956]","synonyms":"OSTbeta","biotype":"protein_coding","ncbi_id":"123264","summary":null,"start":65045370,"end":65053396,"strand":1,"description":"solute carrier family 51 beta subunit [Source:HGNC Symbol;Acc:HGNC:29956]"}, {"versioned_ensembl_gene_id":"ENSG00000255471.1","gene_symbol":"AP001528.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86892214,"end":86925037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280339.1","gene_symbol":"AP001528.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86908990,"end":86912238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265787.2","gene_symbol":"CYP4F35P","gene_name":"cytochrome P450 family 4 subfamily F member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:39954]","synonyms":"CYP4F-se8[6:7:8]","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284233","summary":null,"start":14337423,"end":14342524,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:39954]"}, {"versioned_ensembl_gene_id":"ENSG00000229495.1","gene_symbol":"AL450327.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78809715,"end":78813303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221840.4","gene_symbol":"OR4A5","gene_name":"olfactory receptor family 4 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:15162]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81318","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":54706832,"end":54707902,"strand":1,"description":"olfactory receptor family 4 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:15162]"}, {"versioned_ensembl_gene_id":"ENSG00000226792.7","gene_symbol":"C13orf42","gene_name":"chromosome 13 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:42693]","synonyms":"LINC00371","biotype":"protein_coding","ncbi_id":"647166","summary":null,"start":51082119,"end":51200252,"strand":-1,"description":"chromosome 13 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:42693]"}, {"versioned_ensembl_gene_id":"ENSG00000277618.1","gene_symbol":"AL627230.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67797221,"end":67797500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219253.1","gene_symbol":"AL390316.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77496119,"end":77496671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093183.13","gene_symbol":"SEC22C","gene_name":"SEC22 homolog C, vesicle trafficking protein [Source:HGNC Symbol;Acc:HGNC:16828]","synonyms":"MGC13261,SEC22L3,MGC5373","biotype":"protein_coding","ncbi_id":"9117","summary":"This gene encodes a member of the SEC22 family of vesicle trafficking proteins. The encoded protein is localized to the endoplasmic reticulum and may play a role in the early stages of ER-Golgi protein trafficking. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":42547969,"end":42601080,"strand":-1,"description":"SEC22 homolog C, vesicle trafficking protein [Source:HGNC Symbol;Acc:HGNC:16828]"}, {"versioned_ensembl_gene_id":"ENSG00000225673.3","gene_symbol":"AC104164.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60730055,"end":60730644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204196.5","gene_symbol":"RPL12P16","gene_name":"ribosomal protein L12 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130447","summary":null,"start":203190780,"end":203191277,"strand":1,"description":"ribosomal protein L12 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36926]"}, {"versioned_ensembl_gene_id":"ENSG00000250891.1","gene_symbol":"LINC02208","gene_name":"long intergenic non-protein coding RNA 2208 [Source:HGNC Symbol;Acc:HGNC:52978]","synonyms":"HRAT56","biotype":"lincRNA","ncbi_id":"101927280","summary":null,"start":118468156,"end":118562117,"strand":-1,"description":"long intergenic non-protein coding RNA 2208 [Source:HGNC Symbol;Acc:HGNC:52978]"}, {"versioned_ensembl_gene_id":"ENSG00000066735.14","gene_symbol":"KIF26A","gene_name":"kinesin family member 26A [Source:HGNC Symbol;Acc:HGNC:20226]","synonyms":"KIAA1236,DKFZP434N178","biotype":"protein_coding","ncbi_id":"26153","summary":null,"start":104138723,"end":104180894,"strand":1,"description":"kinesin family member 26A [Source:HGNC Symbol;Acc:HGNC:20226]"}, {"versioned_ensembl_gene_id":"ENSG00000254120.1","gene_symbol":"LINC02155","gene_name":"long intergenic non-protein coding RNA 2155 [Source:HGNC Symbol;Acc:HGNC:53016]","synonyms":"RP11-705O24.1","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61889839,"end":61894206,"strand":1,"description":"long intergenic non-protein coding RNA 2155 [Source:HGNC Symbol;Acc:HGNC:53016]"}, {"versioned_ensembl_gene_id":"ENSG00000248663.6","gene_symbol":"LINC00992","gene_name":"long intergenic non-protein coding RNA 992 [Source:HGNC Symbol;Acc:HGNC:48943]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728342","summary":null,"start":117415509,"end":117546298,"strand":1,"description":"long intergenic non-protein coding RNA 992 [Source:HGNC Symbol;Acc:HGNC:48943]"}, {"versioned_ensembl_gene_id":"ENSG00000196578.4","gene_symbol":"OR5AC2","gene_name":"olfactory receptor family 5 subfamily AC member 2 [Source:HGNC Symbol;Acc:HGNC:15431]","synonyms":"HSA1","biotype":"protein_coding","ncbi_id":"81050","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98087173,"end":98088102,"strand":1,"description":"olfactory receptor family 5 subfamily AC member 2 [Source:HGNC Symbol;Acc:HGNC:15431]"}, {"versioned_ensembl_gene_id":"ENSG00000276204.1","gene_symbol":"BX005195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67328207,"end":67329404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144843.11","gene_symbol":"ADPRH","gene_name":"ADP-ribosylarginine hydrolase [Source:HGNC Symbol;Acc:HGNC:269]","synonyms":"ARH1","biotype":"protein_coding","ncbi_id":"141","summary":"The enzyme encoded by this gene catalyzes removal of mono-ADP-ribose from arginine residues of proteins in the ADP-ribosylation cycle. Unlike the rat and mouse enzymes that require DTT for maximal activity, the human enzyme is DTT-independent. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, May 2014]","start":119579268,"end":119589945,"strand":1,"description":"ADP-ribosylarginine hydrolase [Source:HGNC Symbol;Acc:HGNC:269]"}, {"versioned_ensembl_gene_id":"ENSG00000154640.14","gene_symbol":"BTG3","gene_name":"BTG anti-proliferation factor 3 [Source:HGNC Symbol;Acc:HGNC:1132]","synonyms":"tob55,APRO4,ANA/BTG3,ANA","biotype":"protein_coding","ncbi_id":"10950","summary":"The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein might play a role in neurogenesis in the central nervous system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":17593653,"end":17612947,"strand":-1,"description":"BTG anti-proliferation factor 3 [Source:HGNC Symbol;Acc:HGNC:1132]"}, {"versioned_ensembl_gene_id":"ENSG00000267704.1","gene_symbol":"FRG2LP","gene_name":"FSHD region gene 2 family member L, pseudogene [Source:HGNC Symbol;Acc:HGNC:51798]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480352","summary":null,"start":14137710,"end":14139272,"strand":1,"description":"FSHD region gene 2 family member L, pseudogene [Source:HGNC Symbol;Acc:HGNC:51798]"}, {"versioned_ensembl_gene_id":"ENSG00000225424.1","gene_symbol":"AL391869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129278251,"end":129291722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140525.17","gene_symbol":"FANCI","gene_name":"Fanconi anemia complementation group I [Source:HGNC Symbol;Acc:HGNC:25568]","synonyms":"KIAA1794,FLJ10719","biotype":"protein_coding","ncbi_id":"55215","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group I. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":89243949,"end":89317261,"strand":1,"description":"Fanconi anemia complementation group I [Source:HGNC Symbol;Acc:HGNC:25568]"}, {"versioned_ensembl_gene_id":"ENSG00000232985.1","gene_symbol":"AL355537.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128958772,"end":128960062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213384.2","gene_symbol":"EIF4E2P1","gene_name":"eukaryotic translation initiation factor 4E family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16237]","synonyms":"EIF4EL4,dJ1049G11.3","biotype":"processed_pseudogene","ncbi_id":"128770","summary":null,"start":20659710,"end":20659964,"strand":1,"description":"eukaryotic translation initiation factor 4E family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16237]"}, {"versioned_ensembl_gene_id":"ENSG00000234922.1","gene_symbol":"TSEN15P3","gene_name":"tRNA splicing endonuclease subunit 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43964]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105375192","summary":null,"start":25265924,"end":25266290,"strand":-1,"description":"tRNA splicing endonuclease subunit 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43964]"}, {"versioned_ensembl_gene_id":"ENSG00000081665.13","gene_symbol":"ZNF506","gene_name":"zinc finger protein 506 [Source:HGNC Symbol;Acc:HGNC:23780]","synonyms":"DKFZp761G1812","biotype":"protein_coding","ncbi_id":"440515","summary":null,"start":19785839,"end":19821751,"strand":-1,"description":"zinc finger protein 506 [Source:HGNC Symbol;Acc:HGNC:23780]"}, {"versioned_ensembl_gene_id":"ENSG00000228259.3","gene_symbol":"AC136604.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":179651284,"end":179652457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248799.1","gene_symbol":"AC022118.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127651693,"end":127664029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205279.8","gene_symbol":"CTXN3","gene_name":"cortexin 3 [Source:HGNC Symbol;Acc:HGNC:31110]","synonyms":null,"biotype":"protein_coding","ncbi_id":"613212","summary":null,"start":127649044,"end":127658630,"strand":1,"description":"cortexin 3 [Source:HGNC Symbol;Acc:HGNC:31110]"}, {"versioned_ensembl_gene_id":"ENSG00000168395.15","gene_symbol":"ING5","gene_name":"inhibitor of growth family member 5 [Source:HGNC Symbol;Acc:HGNC:19421]","synonyms":"FLJ23842,p28ING5","biotype":"protein_coding","ncbi_id":"84289","summary":"This gene encodes a tumor suppressor protein that inhibits cell growth and induces apoptosis. This protein contains a PHD-type zinc finger. It interacts with tumor suppressor p53 and p300, a component of the histone acetyl transferase complex, suggesting a role in transcriptional regulation. Alternative splicing and the use of multiple promoters and 3' terminal exons results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":241687085,"end":241729478,"strand":1,"description":"inhibitor of growth family member 5 [Source:HGNC Symbol;Acc:HGNC:19421]"}, {"versioned_ensembl_gene_id":"ENSG00000249861.3","gene_symbol":"LGALS16","gene_name":"galectin 16 [Source:HGNC Symbol;Acc:HGNC:40039]","synonyms":null,"biotype":"protein_coding","ncbi_id":"148003","summary":null,"start":39655894,"end":39660647,"strand":1,"description":"galectin 16 [Source:HGNC Symbol;Acc:HGNC:40039]"}, {"versioned_ensembl_gene_id":"ENSG00000028116.16","gene_symbol":"VRK2","gene_name":"vaccinia related kinase 2 [Source:HGNC Symbol;Acc:HGNC:12719]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7444","summary":"This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. The encoded protein acts as an effector of signaling pathways that regulate apoptosis and tumor cell growth. Variants in this gene have been associated with schizophrenia. Alternative splicing results in multiple transcript variants that differ in their subcellular localization and biological activity. [provided by RefSeq, Jan 2014]","start":57907651,"end":58159920,"strand":1,"description":"vaccinia related kinase 2 [Source:HGNC Symbol;Acc:HGNC:12719]"}, {"versioned_ensembl_gene_id":"ENSG00000258036.2","gene_symbol":"KRT125P","gene_name":"keratin 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:48875]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418828","summary":null,"start":52729517,"end":52736142,"strand":-1,"description":"keratin 125 pseudogene [Source:HGNC Symbol;Acc:HGNC:48875]"}, {"versioned_ensembl_gene_id":"ENSG00000179598.5","gene_symbol":"PLD6","gene_name":"phospholipase D family member 6 [Source:HGNC Symbol;Acc:HGNC:30447]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201164","summary":null,"start":17200995,"end":17206315,"strand":-1,"description":"phospholipase D family member 6 [Source:HGNC Symbol;Acc:HGNC:30447]"}, {"versioned_ensembl_gene_id":"ENSG00000205076.4","gene_symbol":"LGALS7","gene_name":"galectin 7 [Source:HGNC Symbol;Acc:HGNC:6568]","synonyms":"LGALS7A,GAL7,TP53I1,PIG1","biotype":"protein_coding","ncbi_id":"3963","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:653499) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008]","start":38770971,"end":38773492,"strand":-1,"description":"galectin 7 [Source:HGNC Symbol;Acc:HGNC:6568]"}, {"versioned_ensembl_gene_id":"ENSG00000273607.3","gene_symbol":"CHCHD10","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]","synonyms":"N27C7-4,C22orf16","biotype":"protein_coding","ncbi_id":"400916","summary":"This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19. [provided by RefSeq, Aug 2014]","start":23765834,"end":23768443,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]"}, {"versioned_ensembl_gene_id":"ENSG00000243758.1","gene_symbol":"RPL35AP15","gene_name":"ribosomal protein L35a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271317","summary":null,"start":117301104,"end":117301442,"strand":-1,"description":"ribosomal protein L35a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36974]"}, {"versioned_ensembl_gene_id":"ENSG00000267310.2","gene_symbol":"OR4G1P","gene_name":"olfactory receptor family 4 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8302]","synonyms":"OR4G8P,OLB","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26681","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":99175,"end":106077,"strand":1,"description":"olfactory receptor family 4 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8302]"}, {"versioned_ensembl_gene_id":"ENSG00000241921.1","gene_symbol":"AC000372.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126378970,"end":126424185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175322.11","gene_symbol":"ZNF519","gene_name":"zinc finger protein 519 [Source:HGNC Symbol;Acc:HGNC:30574]","synonyms":"HsT2362,FLJ36809","biotype":"protein_coding","ncbi_id":"162655","summary":null,"start":14057457,"end":14132490,"strand":-1,"description":"zinc finger protein 519 [Source:HGNC Symbol;Acc:HGNC:30574]"}, {"versioned_ensembl_gene_id":"ENSG00000134917.9","gene_symbol":"ADAMTS8","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 8 [Source:HGNC Symbol;Acc:HGNC:224]","synonyms":"METH2,FLJ41712,ADAM-TS8","biotype":"protein_coding","ncbi_id":"11095","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme contains two C-terminal TS motifs, and disrupts angiogenesis in vivo. A number of disorders have been mapped in the vicinity of this gene, most notably lung neoplasms. Reduced expression of this gene has been observed in multiple human cancers and this gene has been proposed as a potential tumor suppressor. [provided by RefSeq, Feb 2016]","start":130404925,"end":130428993,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 8 [Source:HGNC Symbol;Acc:HGNC:224]"}, {"versioned_ensembl_gene_id":"ENSG00000230669.6","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32879989,"end":32883975,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000132334.16","gene_symbol":"PTPRE","gene_name":"protein tyrosine phosphatase, receptor type E [Source:HGNC Symbol;Acc:HGNC:9669]","synonyms":"PTPE","biotype":"protein_coding","ncbi_id":"5791","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. Several alternatively spliced transcript variants of this gene have been reported, at least two of which encode a receptor-type PTP that possesses a short extracellular domain, a single transmembrane region, and two tandem intracytoplasmic catalytic domains; another one encodes a PTP that contains a distinct hydrophilic N-terminus, and thus represents a nonreceptor-type isoform of this PTP. Studies of the similar gene in mice suggested the regulatory roles of this PTP in RAS related signal transduction pathways, cytokine-induced SATA signaling, as well as the activation of voltage-gated K+ channels. [provided by RefSeq, Oct 2015]","start":127907061,"end":128085855,"strand":1,"description":"protein tyrosine phosphatase, receptor type E [Source:HGNC Symbol;Acc:HGNC:9669]"}, {"versioned_ensembl_gene_id":"ENSG00000204305.13","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32180968,"end":32184324,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000181896.11","gene_symbol":"ZNF101","gene_name":"zinc finger protein 101 [Source:HGNC Symbol;Acc:HGNC:12881]","synonyms":"HZF12,DKFZp570I0164","biotype":"protein_coding","ncbi_id":"94039","summary":"Zinc finger proteins (ZNFs), such as ZNF101, bind nucleic acids and perform many key functions, the most important of which is regulating transcription (summary by Bellefroid et al., 1993 [PubMed 8467795]). See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Nov 2010]","start":19668796,"end":19683509,"strand":1,"description":"zinc finger protein 101 [Source:HGNC Symbol;Acc:HGNC:12881]"}, {"versioned_ensembl_gene_id":"ENSG00000125848.9","gene_symbol":"FLRT3","gene_name":"fibronectin leucine rich transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3762]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23767","summary":"This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. FLRTs may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. This gene is expressed in many tissues. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2010]","start":14322988,"end":14337616,"strand":-1,"description":"fibronectin leucine rich transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:3762]"}, {"versioned_ensembl_gene_id":"ENSG00000254637.1","gene_symbol":"OR4A18P","gene_name":"olfactory receptor family 4 subfamily A member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:15155]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81325","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49917391,"end":49918478,"strand":-1,"description":"olfactory receptor family 4 subfamily A member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:15155]"}, {"versioned_ensembl_gene_id":"ENSG00000259002.2","gene_symbol":"AL445363.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34541740,"end":34546329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105507.2","gene_symbol":"CABP5","gene_name":"calcium binding protein 5 [Source:HGNC Symbol;Acc:HGNC:13714]","synonyms":"CABP3","biotype":"protein_coding","ncbi_id":"56344","summary":"The product of this gene belongs to a subfamily of calcium binding proteins, which share similarity to calmodulin. Calcium binding proteins are an important component of calcium mediated cellular signal transduction. Expression of this gene is retina-specific. The mouse homolog of this protein has been shown to express in the inner nuclear layer of the retina, suggested its role in neuronal functioning. The specific function of this gene is unknown. [provided by RefSeq, Oct 2009]","start":48029953,"end":48044053,"strand":-1,"description":"calcium binding protein 5 [Source:HGNC Symbol;Acc:HGNC:13714]"}, {"versioned_ensembl_gene_id":"ENSG00000282171.1","gene_symbol":"LINC02210","gene_name":"long intergenic non-protein coding RNA 2210 [Source:NCBI gene;Acc:147081]","synonyms":"CRHR1-IT1,C17orf69,CRHR1-IT1,C17orf69,FLJ25168","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"147081","summary":null,"start":45631949,"end":45659841,"strand":1,"description":"long intergenic non-protein coding RNA 2210 [Source:NCBI gene;Acc:147081]"}, {"versioned_ensembl_gene_id":"ENSG00000230061.2","gene_symbol":"TRPM2-AS","gene_name":"TRPM2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:50758]","synonyms":"TRPM2-AS1","biotype":"antisense_RNA","ncbi_id":"101928607","summary":null,"start":44414588,"end":44425272,"strand":-1,"description":"TRPM2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:50758]"}, {"versioned_ensembl_gene_id":"ENSG00000153914.15","gene_symbol":"SREK1","gene_name":"splicing regulatory glutamic acid and lysine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:17882]","synonyms":"SRrp86,SRrp508,SFRS12,DKFZp564B176","biotype":"protein_coding","ncbi_id":"140890","summary":"This gene encodes a member of a family of serine/arginine-rich (SR) splicing proteins containing RNA recognition motif (RRM) domains. The encoded protein interacts with other SR proteins to modulate splice site selection. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":66139971,"end":66183615,"strand":1,"description":"splicing regulatory glutamic acid and lysine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:17882]"}, {"versioned_ensembl_gene_id":"ENSG00000268738.2","gene_symbol":"HSFX2","gene_name":"heat shock transcription factor family, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:32701]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130086","summary":null,"start":149592515,"end":149594716,"strand":-1,"description":"heat shock transcription factor family, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:32701]"}, {"versioned_ensembl_gene_id":"ENSG00000236156.2","gene_symbol":"CHCHD4P3","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44491]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480792","summary":null,"start":37434177,"end":37434586,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44491]"}, {"versioned_ensembl_gene_id":"ENSG00000282458.1","gene_symbol":"WASH5P","gene_name":"WAS protein family homolog 5 pseudogene [Source:NCBI gene;Acc:375690]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"375690","summary":null,"start":60951,"end":71626,"strand":-1,"description":"WAS protein family homolog 5 pseudogene [Source:NCBI gene;Acc:375690]"}, {"versioned_ensembl_gene_id":"ENSG00000178928.8","gene_symbol":"TPRX1","gene_name":"tetrapeptide repeat homeobox 1 [Source:HGNC Symbol;Acc:HGNC:32174]","synonyms":"FLJ40321","biotype":"protein_coding","ncbi_id":"284355","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the TPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":47801243,"end":47819051,"strand":-1,"description":"tetrapeptide repeat homeobox 1 [Source:HGNC Symbol;Acc:HGNC:32174]"}, {"versioned_ensembl_gene_id":"ENSG00000247199.3","gene_symbol":"AC091948.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148268307,"end":148383783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227496.1","gene_symbol":"AC099066.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":225700604,"end":225752243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254440.3","gene_symbol":"PBOV1","gene_name":"prostate and breast cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:21079]","synonyms":"UROC28,UC28","biotype":"protein_coding","ncbi_id":"59351","summary":"This intronless gene encodes a protein of unknown function. Its expression is up-regulated in some types of cancer, including prostate, breast, and bladder cancer. [provided by RefSeq, Aug 2011]","start":138215986,"end":138218491,"strand":-1,"description":"prostate and breast cancer overexpressed 1 [Source:HGNC Symbol;Acc:HGNC:21079]"}, {"versioned_ensembl_gene_id":"ENSG00000279640.1","gene_symbol":"AC138466.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132100013,"end":132100820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115041.12","gene_symbol":"KCNIP3","gene_name":"potassium voltage-gated channel interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:15523]","synonyms":"KCHIP3,DREAM,CSEN","biotype":"protein_coding","ncbi_id":"30818","summary":"This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins, which belong to the recoverin branch of the EF-hand superfamily. Members of this family are small calcium binding proteins containing EF-hand-like domains. They are integral subunit components of native Kv4 channel complexes that may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. The encoded protein also functions as a calcium-regulated transcriptional repressor, and interacts with presenilins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":95297304,"end":95386083,"strand":1,"description":"potassium voltage-gated channel interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:15523]"}, {"versioned_ensembl_gene_id":"ENSG00000227175.1","gene_symbol":"AL590677.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13528516,"end":13530262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073536.17","gene_symbol":"NLE1","gene_name":"notchless homolog 1 [Source:HGNC Symbol;Acc:HGNC:19889]","synonyms":"NLE,FLJ10458","biotype":"protein_coding","ncbi_id":"54475","summary":null,"start":35128753,"end":35142315,"strand":-1,"description":"notchless homolog 1 [Source:HGNC Symbol;Acc:HGNC:19889]"}, {"versioned_ensembl_gene_id":"ENSG00000243629.1","gene_symbol":"LINC00880","gene_name":"long intergenic non-protein coding RNA 880 [Source:HGNC Symbol;Acc:HGNC:27948]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339894","summary":null,"start":157081667,"end":157123004,"strand":-1,"description":"long intergenic non-protein coding RNA 880 [Source:HGNC Symbol;Acc:HGNC:27948]"}, {"versioned_ensembl_gene_id":"ENSG00000241777.1","gene_symbol":"AC092185.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":108725440,"end":108725536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105373.18","gene_symbol":"NOP53","gene_name":"NOP53 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:4333]","synonyms":"PICT1,PICT-1,GLTSCR2","biotype":"protein_coding","ncbi_id":"29997","summary":null,"start":47745522,"end":47757058,"strand":1,"description":"NOP53 ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:4333]"}, {"versioned_ensembl_gene_id":"ENSG00000242752.3","gene_symbol":"NMTRQ-TTG12-1","gene_name":"nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 12-1 [Source:HGNC Symbol;Acc:HGNC:35051]","synonyms":"TRNAQ41P","biotype":"unprocessed_pseudogene","ncbi_id":"100189478","summary":null,"start":19603274,"end":19603345,"strand":-1,"description":"nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 12-1 [Source:HGNC Symbol;Acc:HGNC:35051]"}, {"versioned_ensembl_gene_id":"ENSG00000237816.1","gene_symbol":"RPL21P109","gene_name":"ribosomal protein L21 pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:36388]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271437","summary":null,"start":71704181,"end":71704655,"strand":1,"description":"ribosomal protein L21 pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:36388]"}, {"versioned_ensembl_gene_id":"ENSG00000227563.1","gene_symbol":"RNF11P2","gene_name":"ring finger protein 11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16535]","synonyms":"RNF11B,bA280O9.1","biotype":"processed_pseudogene","ncbi_id":"170543","summary":null,"start":14547184,"end":14547623,"strand":-1,"description":"ring finger protein 11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16535]"}, {"versioned_ensembl_gene_id":"ENSG00000227172.2","gene_symbol":"AC011290.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39545646,"end":39566239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224782.8","gene_symbol":"PFDN6","gene_name":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]","synonyms":"HKE2,H2-KE2,PFD6,KE-2","biotype":"protein_coding","ncbi_id":"10471","summary":"PFDN6 is a subunit of the heteromeric prefoldin complex that chaperones nascent actin (see MIM 102560) and alpha- and beta-tubulin (see MIM 602529 and MIM 191130, respectively) chains pending their transfer to the cytosolic chaperonin containing TCP1 (MIM 186980) (CCT) complex (Hansen et al., 1999 [PubMed 10209023]).[supplied by OMIM, Jul 2010]","start":33267227,"end":33276326,"strand":1,"description":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]"}, {"versioned_ensembl_gene_id":"ENSG00000251545.2","gene_symbol":"AC136628.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":179522457,"end":179525074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273012.1","gene_symbol":"AL353600.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33341655,"end":33341905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133067.17","gene_symbol":"LGR6","gene_name":"leucine rich repeat containing G protein-coupled receptor 6 [Source:HGNC Symbol;Acc:HGNC:19719]","synonyms":"FLJ14471","biotype":"protein_coding","ncbi_id":"59352","summary":"This gene encodes a member of the leucine-rich repeat-containing subgroup of the G protein-coupled 7-transmembrane protein superfamily. The encoded protein is a glycoprotein hormone receptor with a large N-terminal extracellular domain that contains leucine-rich repeats important for the formation of a horseshoe-shaped interaction motif for ligand binding. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":202193901,"end":202319781,"strand":1,"description":"leucine rich repeat containing G protein-coupled receptor 6 [Source:HGNC Symbol;Acc:HGNC:19719]"}, {"versioned_ensembl_gene_id":"ENSG00000275964.1","gene_symbol":"AL355001.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19863858,"end":19865048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258366.7","gene_symbol":"RTEL1","gene_name":"regulator of telomere elongation helicase 1 [Source:HGNC Symbol;Acc:HGNC:15888]","synonyms":"RTEL,NHL,KIAA1088,DKFZP434C013,C20orf41,bK3184A7.3","biotype":"protein_coding","ncbi_id":"51750","summary":"This gene encodes a DNA helicase which functions in the stability, protection and elongation of telomeres and interacts with proteins in the shelterin complex known to protect telomeres during DNA replication. Mutations in this gene have been associated with dyskeratosis congenita and Hoyerall-Hreidarsson syndrome. Read-through transcription of this gene into the neighboring downstream gene, which encodes tumor necrosis factor receptor superfamily, member 6b, generates a non-coding transcript. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013]","start":63657810,"end":63696253,"strand":1,"description":"regulator of telomere elongation helicase 1 [Source:HGNC Symbol;Acc:HGNC:15888]"}, {"versioned_ensembl_gene_id":"ENSG00000254685.6","gene_symbol":"FPGT","gene_name":"fucose-1-phosphate guanylyltransferase [Source:HGNC Symbol;Acc:HGNC:3825]","synonyms":"GFPP","biotype":"protein_coding","ncbi_id":"8790","summary":"L-fucose is a key sugar in glycoproteins and other complex carbohydrates since it may be involved in many of the functional roles of these macromolecules, such as in cell-cell recognition. The fucosyl donor for these fucosylated oligosaccharides is GDP-beta-L-fucose. There are two alternate pathways for the biosynthesis of GDP-fucose; the major pathway converts GDP-alpha-D-mannose to GDP-beta-L-fucose. The protein encoded by this gene participates in an alternate pathway that is present in certain mammalian tissues, such as liver and kidney, and appears to function as a salvage pathway to reutilize L-fucose arising from the turnover of glycoproteins and glycolipids. This pathway involves the phosphorylation of L-fucose to form beta-L-fucose-1-phosphate, and then condensation of the beta-L-fucose-1-phosphate with GTP by fucose-1-phosphate guanylyltransferase to form GDP-beta-L-fucose. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring downstream TNNI3 interacting kinase (TNNI3K) gene. [provided by RefSeq, Dec 2010]","start":74198212,"end":74234086,"strand":1,"description":"fucose-1-phosphate guanylyltransferase [Source:HGNC Symbol;Acc:HGNC:3825]"}, {"versioned_ensembl_gene_id":"ENSG00000100941.8","gene_symbol":"PNN","gene_name":"pinin, desmosome associated protein [Source:HGNC Symbol;Acc:HGNC:9162]","synonyms":"memA","biotype":"protein_coding","ncbi_id":"5411","summary":null,"start":39175183,"end":39183218,"strand":1,"description":"pinin, desmosome associated protein [Source:HGNC Symbol;Acc:HGNC:9162]"}, {"versioned_ensembl_gene_id":"ENSG00000250956.1","gene_symbol":"AC011416.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127179756,"end":127179900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259361.5","gene_symbol":"LINC00927","gene_name":"long intergenic non-protein coding RNA 927 [Source:HGNC Symbol;Acc:HGNC:27522]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283688","summary":null,"start":80263068,"end":80341805,"strand":-1,"description":"long intergenic non-protein coding RNA 927 [Source:HGNC Symbol;Acc:HGNC:27522]"}, {"versioned_ensembl_gene_id":"ENSG00000253869.1","gene_symbol":"PIGFP1","gene_name":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8963]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5282","summary":null,"start":178922064,"end":178922716,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8963]"}, {"versioned_ensembl_gene_id":"ENSG00000184182.18","gene_symbol":"UBE2F","gene_name":"ubiquitin conjugating enzyme E2 F (putative) [Source:HGNC Symbol;Acc:HGNC:12480]","synonyms":"NCE2","biotype":"protein_coding","ncbi_id":"140739","summary":null,"start":237966827,"end":238042782,"strand":1,"description":"ubiquitin conjugating enzyme E2 F (putative) [Source:HGNC Symbol;Acc:HGNC:12480]"}, {"versioned_ensembl_gene_id":"ENSG00000203864.3","gene_symbol":"C1orf137","gene_name":"chromosome 1 open reading frame 137 [Source:HGNC Symbol;Acc:HGNC:32040]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388667","summary":null,"start":116694112,"end":116706603,"strand":1,"description":"chromosome 1 open reading frame 137 [Source:HGNC Symbol;Acc:HGNC:32040]"}, {"versioned_ensembl_gene_id":"ENSG00000250286.1","gene_symbol":"AC021491.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":50537294,"end":50538754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226027.1","gene_symbol":"HLA-S","gene_name":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]","synonyms":"HLA-17","biotype":"unprocessed_pseudogene","ncbi_id":"267015","summary":null,"start":31375802,"end":31376019,"strand":-1,"description":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]"}, {"versioned_ensembl_gene_id":"ENSG00000196557.12","gene_symbol":"CACNA1H","gene_name":"calcium voltage-gated channel subunit alpha1 H [Source:HGNC Symbol;Acc:HGNC:1395]","synonyms":"Cav3.2","biotype":"protein_coding","ncbi_id":"8912","summary":"This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE). [provided by RefSeq, Jul 2008]","start":1153121,"end":1221772,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 H [Source:HGNC Symbol;Acc:HGNC:1395]"}, {"versioned_ensembl_gene_id":"ENSG00000224122.1","gene_symbol":"POU6F2-AS1","gene_name":"POU6F2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40979]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861520","summary":null,"start":39404598,"end":39406346,"strand":-1,"description":"POU6F2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40979]"}, {"versioned_ensembl_gene_id":"ENSG00000232560.6","gene_symbol":"LINC01549","gene_name":"long intergenic non-protein coding RNA 1549 [Source:HGNC Symbol;Acc:HGNC:1277]","synonyms":"C21orf37","biotype":"lincRNA","ncbi_id":"100505929","summary":null,"start":17438890,"end":17449185,"strand":1,"description":"long intergenic non-protein coding RNA 1549 [Source:HGNC Symbol;Acc:HGNC:1277]"}, {"versioned_ensembl_gene_id":"ENSG00000182196.13","gene_symbol":"ARL6IP4","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:18076]","synonyms":"SR-25,SFRS20,SRrp37,SRp25","biotype":"protein_coding","ncbi_id":"51329","summary":null,"start":122980060,"end":122982913,"strand":1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:18076]"}, {"versioned_ensembl_gene_id":"ENSG00000272180.1","gene_symbol":"AC011306.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55952158,"end":56181652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189014.7","gene_symbol":"FAM35DP","gene_name":"family with sequence similarity 35 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:34038]","synonyms":"FAM35B2","biotype":"unprocessed_pseudogene","ncbi_id":"439965","summary":null,"start":47689707,"end":47730436,"strand":1,"description":"family with sequence similarity 35 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:34038]"}, {"versioned_ensembl_gene_id":"ENSG00000233242.2","gene_symbol":"AL512604.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37112548,"end":37115490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180758.11","gene_symbol":"GPR157","gene_name":"G protein-coupled receptor 157 [Source:HGNC Symbol;Acc:HGNC:23687]","synonyms":"FLJ12132","biotype":"protein_coding","ncbi_id":"80045","summary":null,"start":9100305,"end":9129170,"strand":-1,"description":"G protein-coupled receptor 157 [Source:HGNC Symbol;Acc:HGNC:23687]"}, {"versioned_ensembl_gene_id":"ENSG00000266217.2","gene_symbol":"CTSLP2","gene_name":"cathepsin L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2540]","synonyms":"CTSLL7,bA144G6.6,CTSLP5,CTSLL5,CTSLL7,CTSLL2,CTSLL5,CTSL1P7,CTSLL2,CTSL1P5,CTSL1P7,CTSL1P2,CTSL1P5,bA342C24.4,CTSLP7,CTSL1P2,bA144G6.6,CTSLP5,bA342C24.4,CTSLP7","biotype":"unprocessed_pseudogene","ncbi_id":"1517","summary":null,"start":47581211,"end":47582321,"strand":-1,"description":"cathepsin L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2540]"}, {"versioned_ensembl_gene_id":"ENSG00000277633.5","gene_symbol":"IGHG1","gene_name":"immunoglobulin heavy constant gamma 1 (G1m marker) [Source:HGNC Symbol;Acc:HGNC:5525]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3500","summary":null,"start":105737114,"end":105743842,"strand":-1,"description":"immunoglobulin heavy constant gamma 1 (G1m marker) [Source:HGNC Symbol;Acc:HGNC:5525]"}, {"versioned_ensembl_gene_id":"ENSG00000270920.1","gene_symbol":"MCRIP2P2","gene_name":"MAPK regulated corepressor interacting protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49631]","synonyms":"MCRIP2P1,FAM195DP","biotype":"processed_pseudogene","ncbi_id":"106480278","summary":null,"start":185435839,"end":185436047,"strand":1,"description":"MAPK regulated corepressor interacting protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49631]"}, {"versioned_ensembl_gene_id":"ENSG00000241984.2","gene_symbol":"RPL7AP2","gene_name":"ribosomal protein L7a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652978","summary":null,"start":39156742,"end":39157852,"strand":1,"description":"ribosomal protein L7a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23552]"}, {"versioned_ensembl_gene_id":"ENSG00000249977.1","gene_symbol":"AC106748.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97449358,"end":97449741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234476.1","gene_symbol":"AC092811.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":225447243,"end":225465343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270778.1","gene_symbol":"BUB1P1","gene_name":"BUB1 mitotic checkpoint serine/threonine kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49529]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422363","summary":null,"start":127867881,"end":127868487,"strand":1,"description":"BUB1 mitotic checkpoint serine/threonine kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49529]"}, {"versioned_ensembl_gene_id":"ENSG00000148225.15","gene_symbol":"WDR31","gene_name":"WD repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:21421]","synonyms":"FLJ35921","biotype":"protein_coding","ncbi_id":"114987","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":113313222,"end":113340298,"strand":-1,"description":"WD repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:21421]"}, {"versioned_ensembl_gene_id":"ENSG00000238097.1","gene_symbol":"LINC02037","gene_name":"long intergenic non-protein coding RNA 2037 [Source:HGNC Symbol;Acc:HGNC:52877]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929337","summary":null,"start":194247648,"end":194257772,"strand":1,"description":"long intergenic non-protein coding RNA 2037 [Source:HGNC Symbol;Acc:HGNC:52877]"}, {"versioned_ensembl_gene_id":"ENSG00000279743.1","gene_symbol":"AC002090.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51761260,"end":51763397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228983.9","gene_symbol":"SLC47A1P1","gene_name":"solute carrier family 47 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51849]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107075108","summary":null,"start":19579943,"end":19596058,"strand":1,"description":"solute carrier family 47 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51849]"}, {"versioned_ensembl_gene_id":"ENSG00000226993.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"POLR2LP,AB023060.6","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31133236,"end":31133422,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000151445.15","gene_symbol":"VIPAS39","gene_name":"VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog [Source:HGNC Symbol;Acc:HGNC:20347]","synonyms":"C14orf133,VPS16B,VIPAR,SPE39,SPE-39,hSPE-39","biotype":"protein_coding","ncbi_id":"63894","summary":"This gene encodes a protein involved in the sorting of lysosomal proteins. Mutations in this gene are associated with ARCS2 (arthrogryposis, renal dysfunction, and cholestasis-2). Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]","start":77426675,"end":77457952,"strand":-1,"description":"VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog [Source:HGNC Symbol;Acc:HGNC:20347]"}, {"versioned_ensembl_gene_id":"ENSG00000255119.1","gene_symbol":"AP003385.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67605521,"end":67606642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180596.7","gene_symbol":"HIST1H2BC","gene_name":"histone cluster 1 H2B family member c [Source:HGNC Symbol;Acc:HGNC:4757]","synonyms":"H2BFL,H2B/l,H2B.1","biotype":"protein_coding","ncbi_id":"8347","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. The protein has antibacterial and antifungal antimicrobial activity. The main transcript variant of this gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. This transcript variant lacks a polyA tail but instead contains a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Apr 2020]","start":26114873,"end":26123926,"strand":-1,"description":"histone cluster 1 H2B family member c [Source:HGNC Symbol;Acc:HGNC:4757]"}, {"versioned_ensembl_gene_id":"ENSG00000185940.10","gene_symbol":"KRTAP5-5","gene_name":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]","synonyms":"KRTAP5.5,KRTAP5-11","biotype":"protein_coding","ncbi_id":"439915","summary":null,"start":1629775,"end":1630707,"strand":1,"description":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]"}, {"versioned_ensembl_gene_id":"ENSG00000258520.1","gene_symbol":"AL359317.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69239166,"end":69260567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225678.2","gene_symbol":"AP000619.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":102751070,"end":102754943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260063.1","gene_symbol":"AL512408.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26692132,"end":26694131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229964.1","gene_symbol":"AC080129.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194091561,"end":194109174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141968.7","gene_symbol":"VAV1","gene_name":"vav guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:12657]","synonyms":"VAV","biotype":"protein_coding","ncbi_id":"7409","summary":"This gene is a member of the VAV gene family. The VAV proteins are guanine nucleotide exchange factors (GEFs) for Rho family GTPases that activate pathways leading to actin cytoskeletal rearrangements and transcriptional alterations. The encoded protein is important in hematopoiesis, playing a role in T-cell and B-cell development and activation. The encoded protein has been identified as the specific binding partner of Nef proteins from HIV-1. Coexpression and binding of these partners initiates profound morphological changes, cytoskeletal rearrangements and the JNK/SAPK signaling cascade, leading to increased levels of viral transcription and replication. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2012]","start":6772714,"end":6857366,"strand":1,"description":"vav guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:12657]"}, {"versioned_ensembl_gene_id":"ENSG00000233973.6","gene_symbol":"LINC01360","gene_name":"long intergenic non-protein coding RNA 1360 [Source:HGNC Symbol;Acc:HGNC:50593]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927295","summary":null,"start":73306170,"end":73355253,"strand":1,"description":"long intergenic non-protein coding RNA 1360 [Source:HGNC Symbol;Acc:HGNC:50593]"}, {"versioned_ensembl_gene_id":"ENSG00000229636.2","gene_symbol":"KRT8P21","gene_name":"keratin 8 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:33373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126811","summary":null,"start":73104792,"end":73106282,"strand":1,"description":"keratin 8 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:33373]"}, {"versioned_ensembl_gene_id":"ENSG00000277501.1","gene_symbol":"AC243571.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37642947,"end":37684252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151883.17","gene_symbol":"PARP8","gene_name":"poly(ADP-ribose) polymerase family member 8 [Source:HGNC Symbol;Acc:HGNC:26124]","synonyms":"pART16,FLJ21308","biotype":"protein_coding","ncbi_id":"79668","summary":null,"start":50665899,"end":50846522,"strand":1,"description":"poly(ADP-ribose) polymerase family member 8 [Source:HGNC Symbol;Acc:HGNC:26124]"}, {"versioned_ensembl_gene_id":"ENSG00000113739.10","gene_symbol":"STC2","gene_name":"stanniocalcin 2 [Source:HGNC Symbol;Acc:HGNC:11374]","synonyms":"STC-2","biotype":"protein_coding","ncbi_id":"8614","summary":"This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The encoded protein has 10 of its 15 cysteine residues conserved among stanniocalcin family members and is phosphorylated by casein kinase 2 exclusively on its serine residues. Its C-terminus contains a cluster of histidine residues which may interact with metal ions. The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/phosphate homeostasis. Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast cancers. [provided by RefSeq, Jul 2008]","start":173314713,"end":173329503,"strand":-1,"description":"stanniocalcin 2 [Source:HGNC Symbol;Acc:HGNC:11374]"}, {"versioned_ensembl_gene_id":"ENSG00000197312.11","gene_symbol":"DDI2","gene_name":"DNA damage inducible 1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:24578]","synonyms":"MGC14844","biotype":"protein_coding","ncbi_id":"84301","summary":null,"start":15617500,"end":15669044,"strand":1,"description":"DNA damage inducible 1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:24578]"}, {"versioned_ensembl_gene_id":"ENSG00000226949.1","gene_symbol":"OR6K5P","gene_name":"olfactory receptor family 6 subfamily K member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15032]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391115","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158742146,"end":158743415,"strand":-1,"description":"olfactory receptor family 6 subfamily K member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15032]"}, {"versioned_ensembl_gene_id":"ENSG00000239974.6","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"C6orf8,NG3","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32172254,"end":32175953,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000180437.5","gene_symbol":"OR6K4P","gene_name":"olfactory receptor family 6 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15031]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"128370","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158724113,"end":158725067,"strand":-1,"description":"olfactory receptor family 6 subfamily K member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15031]"}, {"versioned_ensembl_gene_id":"ENSG00000269054.1","gene_symbol":"AC012313.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58362585,"end":58366591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213614.9","gene_symbol":"HEXA","gene_name":"hexosaminidase subunit alpha [Source:HGNC Symbol;Acc:HGNC:4878]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3073","summary":"This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I). Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":72340919,"end":72376476,"strand":-1,"description":"hexosaminidase subunit alpha [Source:HGNC Symbol;Acc:HGNC:4878]"}, {"versioned_ensembl_gene_id":"ENSG00000268895.5","gene_symbol":"A1BG-AS1","gene_name":"A1BG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37133]","synonyms":"FLJ23569,A1BGAS,A1BG-AS,NCRNA00181","biotype":"antisense_RNA","ncbi_id":"503538","summary":null,"start":58347751,"end":58355183,"strand":1,"description":"A1BG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37133]"}, {"versioned_ensembl_gene_id":"ENSG00000197038.6","gene_symbol":"RBMY1A3P","gene_name":"RNA binding motif protein, Y-linked, family 1, member A3 pseudogene [Source:HGNC Symbol;Acc:HGNC:18849]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"286557","summary":null,"start":9311130,"end":9322869,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 1, member A3 pseudogene [Source:HGNC Symbol;Acc:HGNC:18849]"}, {"versioned_ensembl_gene_id":"ENSG00000254200.1","gene_symbol":"AC008412.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173225836,"end":173226423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232924.1","gene_symbol":"ELOCP4","gene_name":"elongin C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38141]","synonyms":"TCEB1P4","biotype":"processed_pseudogene","ncbi_id":"100462873","summary":null,"start":9230915,"end":9231247,"strand":1,"description":"elongin C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38141]"}, {"versioned_ensembl_gene_id":"ENSG00000230223.6","gene_symbol":"ATXN8OS","gene_name":"ATXN8 opposite strand (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:10561]","synonyms":"SCA8,NCRNA00003,KLHL1AS","biotype":"antisense_RNA","ncbi_id":"6315","summary":"This gene is an antisense transcript to the KLHL1 gene (homolog to the Drosophila KELCH gene); it does not itself appear to be protein coding. A TAC/TGC trinucleotide repeat expansion that is incorporated into this gene transcript, but not the KLHL1 transcript, causes spinocerebellar ataxia type 8. Presumably the expansion interferes with normal antisense function of this transcript. [provided by RefSeq, Oct 2008]","start":70107213,"end":70139429,"strand":1,"description":"ATXN8 opposite strand (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:10561]"}, {"versioned_ensembl_gene_id":"ENSG00000162522.10","gene_symbol":"KIAA1522","gene_name":"KIAA1522 [Source:HGNC Symbol;Acc:HGNC:29301]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57648","summary":null,"start":32741885,"end":32774970,"strand":1,"description":"KIAA1522 [Source:HGNC Symbol;Acc:HGNC:29301]"}, {"versioned_ensembl_gene_id":"ENSG00000204498.10","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"IKBL,NFKBIL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31546870,"end":31558829,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000100401.19","gene_symbol":"RANGAP1","gene_name":"Ran GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:9854]","synonyms":"SD,KIAA1835,Fug1","biotype":"protein_coding","ncbi_id":"5905","summary":"This gene encodes a protein that associates with the nuclear pore complex and participates in the regulation of nuclear transport. The encoded protein interacts with Ras-related nuclear protein 1 (RAN) and regulates guanosine triphosphate (GTP)-binding and exchange. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":41245611,"end":41286251,"strand":-1,"description":"Ran GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:9854]"}, {"versioned_ensembl_gene_id":"ENSG00000122783.16","gene_symbol":"C7orf49","gene_name":"chromosome 7 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:22432]","synonyms":"MRI-2,MRI,MGC5242,FLJ27285,FLJ22450","biotype":"protein_coding","ncbi_id":"78996","summary":null,"start":135092363,"end":135170795,"strand":-1,"description":"chromosome 7 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:22432]"}, {"versioned_ensembl_gene_id":"ENSG00000259179.1","gene_symbol":"UBE2CP4","gene_name":"ubiquitin conjugating enzyme E2 C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283711","summary":null,"start":31420128,"end":31420662,"strand":1,"description":"ubiquitin conjugating enzyme E2 C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43553]"}, {"versioned_ensembl_gene_id":"ENSG00000236672.6","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32383385,"end":32438560,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000175325.2","gene_symbol":"PROP1","gene_name":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5626","summary":"This gene encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Expression occurs prior to and is required for expression of pou domain transcription factor 1, which is responsible for pituitary development and hormone expression. Mutations in this gene have been associated with combined pituitary hormone deficiency-2 as well as deficiencies in luteinizing hormone, follicle-stimulating hormone, growth hormone, prolactin, and thyroid-stimulating hormone. [provided by RefSeq, Sep 2011]","start":177992235,"end":177996242,"strand":-1,"description":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]"}, {"versioned_ensembl_gene_id":"ENSG00000203795.2","gene_symbol":"FAM24A","gene_name":"family with sequence similarity 24 member A [Source:HGNC Symbol;Acc:HGNC:23470]","synonyms":"AC073585.4","biotype":"protein_coding","ncbi_id":"118670","summary":null,"start":122910701,"end":122913111,"strand":1,"description":"family with sequence similarity 24 member A [Source:HGNC Symbol;Acc:HGNC:23470]"}, {"versioned_ensembl_gene_id":"ENSG00000243319.7","gene_symbol":"FGF14-IT1","gene_name":"FGF14 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42774]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"283480","summary":null,"start":102292327,"end":102394519,"strand":-1,"description":"FGF14 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42774]"}, {"versioned_ensembl_gene_id":"ENSG00000236860.1","gene_symbol":"RPL39P29","gene_name":"ribosomal protein L39 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35808]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271522","summary":null,"start":102263046,"end":102263202,"strand":-1,"description":"ribosomal protein L39 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35808]"}, {"versioned_ensembl_gene_id":"ENSG00000175398.2","gene_symbol":"OR10P1","gene_name":"olfactory receptor family 10 subfamily P member 1 [Source:HGNC Symbol;Acc:HGNC:15378]","synonyms":"OST701,OR10P3P,OR10P2P,OR10P1P","biotype":"protein_coding","ncbi_id":"121130","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55636860,"end":55637854,"strand":1,"description":"olfactory receptor family 10 subfamily P member 1 [Source:HGNC Symbol;Acc:HGNC:15378]"}, {"versioned_ensembl_gene_id":"ENSG00000229432.2","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31103717,"end":31105053,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000166136.15","gene_symbol":"NDUFB8","gene_name":"NADH:ubiquinone oxidoreductase subunit B8 [Source:HGNC Symbol;Acc:HGNC:7703]","synonyms":"ASHI,CI-ASHI","biotype":"protein_coding","ncbi_id":"4714","summary":null,"start":100523740,"end":100530000,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B8 [Source:HGNC Symbol;Acc:HGNC:7703]"}, {"versioned_ensembl_gene_id":"ENSG00000272937.2","gene_symbol":"AC009779.8","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55608043,"end":55615878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273269.2","gene_symbol":"STPG4","gene_name":"sperm-tail PG-rich repeat containing 4 [Source:NCBI gene;Acc:285051]","synonyms":"FLJ40172,C2orf61,C2orf61","biotype":"protein_coding","ncbi_id":"285051","summary":null,"start":47065941,"end":47176511,"strand":-1,"description":"sperm-tail PG-rich repeat containing 4 [Source:NCBI gene;Acc:285051]"}, {"versioned_ensembl_gene_id":"ENSG00000229910.1","gene_symbol":"HNRNPA1P18","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39445]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874400","summary":null,"start":68301605,"end":68303302,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39445]"}, {"versioned_ensembl_gene_id":"ENSG00000213013.4","gene_symbol":"RPS15AP36","gene_name":"ribosomal protein S15a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271650","summary":null,"start":58216180,"end":58216561,"strand":1,"description":"ribosomal protein S15a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36803]"}, {"versioned_ensembl_gene_id":"ENSG00000231478.1","gene_symbol":"FCF1P9","gene_name":"FCF1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44621]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106480444","summary":null,"start":86481532,"end":86481813,"strand":1,"description":"FCF1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44621]"}, {"versioned_ensembl_gene_id":"ENSG00000226537.2","gene_symbol":"OR7E33P","gene_name":"olfactory receptor family 7 subfamily E member 33 pseudogene [Source:HGNC Symbol;Acc:HGNC:8406]","synonyms":"hg688","biotype":"unprocessed_pseudogene","ncbi_id":"26640","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":67910986,"end":67911951,"strand":1,"description":"olfactory receptor family 7 subfamily E member 33 pseudogene [Source:HGNC Symbol;Acc:HGNC:8406]"}, {"versioned_ensembl_gene_id":"ENSG00000275768.1","gene_symbol":"SLC2AXP1","gene_name":"solute carrier family 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31077]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"399496","summary":null,"start":95196449,"end":95197357,"strand":-1,"description":"solute carrier family 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31077]"}, {"versioned_ensembl_gene_id":"ENSG00000279619.1","gene_symbol":"AC020907.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35137645,"end":35139580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221857.7","gene_symbol":"AC020907.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":35138824,"end":35151336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272564.1","gene_symbol":"AC012511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85904279,"end":85904727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251320.1","gene_symbol":"AC011352.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147887112,"end":147887704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133773.11","gene_symbol":"CCDC59","gene_name":"coiled-coil domain containing 59 [Source:HGNC Symbol;Acc:HGNC:25005]","synonyms":"TAP26,HSPC128,BR22","biotype":"protein_coding","ncbi_id":"29080","summary":null,"start":82223681,"end":82358805,"strand":-1,"description":"coiled-coil domain containing 59 [Source:HGNC Symbol;Acc:HGNC:25005]"}, {"versioned_ensembl_gene_id":"ENSG00000196305.17","gene_symbol":"IARS","gene_name":"isoleucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:5330]","synonyms":"ILRS,IARS1","biotype":"protein_coding","ncbi_id":"3376","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Isoleucine-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family and has been identified as a target of autoantibodies in the autoimmune disease polymyositis/dermatomyositis. Alternatively spliced transcript variants have been found. [provided by RefSeq, Nov 2012]","start":92210207,"end":92293756,"strand":-1,"description":"isoleucyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:5330]"}, {"versioned_ensembl_gene_id":"ENSG00000124733.3","gene_symbol":"MEA1","gene_name":"male-enhanced antigen 1 [Source:HGNC Symbol;Acc:HGNC:6986]","synonyms":"MEA","biotype":"protein_coding","ncbi_id":"4201","summary":null,"start":43012094,"end":43013968,"strand":-1,"description":"male-enhanced antigen 1 [Source:HGNC Symbol;Acc:HGNC:6986]"}, {"versioned_ensembl_gene_id":"ENSG00000235933.1","gene_symbol":"LINC01779","gene_name":"long intergenic non-protein coding RNA 1779 [Source:HGNC Symbol;Acc:HGNC:52569]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985190","summary":null,"start":116164284,"end":116166241,"strand":1,"description":"long intergenic non-protein coding RNA 1779 [Source:HGNC Symbol;Acc:HGNC:52569]"}, {"versioned_ensembl_gene_id":"ENSG00000266744.1","gene_symbol":"AC005304.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13957748,"end":13966952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132507.17","gene_symbol":"EIF5A","gene_name":"eukaryotic translation initiation factor 5A [Source:HGNC Symbol;Acc:HGNC:3300]","synonyms":"MGC99547,MGC104255,EIF5A1,EIF-5A","biotype":"protein_coding","ncbi_id":"1984","summary":null,"start":7306999,"end":7312463,"strand":1,"description":"eukaryotic translation initiation factor 5A [Source:HGNC Symbol;Acc:HGNC:3300]"}, {"versioned_ensembl_gene_id":"ENSG00000027847.13","gene_symbol":"B4GALT7","gene_name":"beta-1,4-galactosyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:930]","synonyms":"XGALT-1,beta4Gal-T7","biotype":"protein_coding","ncbi_id":"11285","summary":"This gene is a member of the beta-1,4-galactosyltransferase (beta4GalT) family. Family members encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose. Each beta4GalT member has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus which then remains uncleaved to function as a transmembrane anchor. The enzyme encoded by this gene attaches the first galactose in the common carbohydrate-protein linkage (GlcA-beta1,3-Gal-beta1,3-Gal-beta1,4-Xyl-beta1-O-Ser) found in proteoglycans. This enzyme differs from other beta4GalTs because it lacks the conserved Cys residues found in beta4GalT1-beta4GalT6 and it is located in cis-Golgi instead of trans-Golgi. Mutations in this gene have been associated with the progeroid form of Ehlers-Danlos syndrome. [provided by RefSeq, Oct 2009]","start":177600100,"end":177610347,"strand":1,"description":"beta-1,4-galactosyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:930]"}, {"versioned_ensembl_gene_id":"ENSG00000130717.12","gene_symbol":"UCK1","gene_name":"uridine-cytidine kinase 1 [Source:HGNC Symbol;Acc:HGNC:14859]","synonyms":"URK1,FLJ12255","biotype":"protein_coding","ncbi_id":"83549","summary":"This gene encodes a uridine-cytidine kinase that catalyzes the phosphorylation of uridine and cytidine to uridine monophosphate (UMP) and cytidine monophosphate (CMP) but not the phosphorylation of deoxyribonucleosides or purine ribonucleosides. This enzyme can also phosphorylate uridine and cytidine analogs and uses both ATP and GTP as a phosphate donor. Alternative splicing results in multiple splice variants encoding distinct isoforms. [provided by RefSeq, May 2012]","start":131523801,"end":131531268,"strand":-1,"description":"uridine-cytidine kinase 1 [Source:HGNC Symbol;Acc:HGNC:14859]"}, {"versioned_ensembl_gene_id":"ENSG00000135775.13","gene_symbol":"COG2","gene_name":"component of oligomeric golgi complex 2 [Source:HGNC Symbol;Acc:HGNC:6546]","synonyms":"LDLC","biotype":"protein_coding","ncbi_id":"22796","summary":"This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi complex. The encoded protein specifically interacts with the USO1 vesicle docking protein and may be necessary for normal Golgi ribbon formation and trafficking of Golgi enzymes. Mutations of this gene are associated with abnormal glycosylation within the Golgi apparatus. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]","start":230642489,"end":230693982,"strand":1,"description":"component of oligomeric golgi complex 2 [Source:HGNC Symbol;Acc:HGNC:6546]"}, {"versioned_ensembl_gene_id":"ENSG00000233902.1","gene_symbol":"AL645933.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31462728,"end":31463336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267467.3","gene_symbol":"APOC4","gene_name":"apolipoprotein C4 [Source:HGNC Symbol;Acc:HGNC:611]","synonyms":null,"biotype":"protein_coding","ncbi_id":"346","summary":"This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene. [provided by RefSeq, Mar 2011]","start":44942238,"end":44945496,"strand":1,"description":"apolipoprotein C4 [Source:HGNC Symbol;Acc:HGNC:611]"}, {"versioned_ensembl_gene_id":"ENSG00000143851.15","gene_symbol":"PTPN7","gene_name":"protein tyrosine phosphatase, non-receptor type 7 [Source:HGNC Symbol;Acc:HGNC:9659]","synonyms":"LC-PTP,HEPTP","biotype":"protein_coding","ncbi_id":"5778","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This gene is preferentially expressed in a variety of hematopoietic cells, and is an early response gene in lymphokine stimulated cells. The non-catalytic N-terminus of this PTP can interact with MAP kinases and suppress the MAP kinase activities. This PTP was shown to be involved in the regulation of T cell antigen receptor (TCR) signaling, which was thought to function through dephosphorylating the molecules related to MAP kinase pathway. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2010]","start":202147013,"end":202161588,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 7 [Source:HGNC Symbol;Acc:HGNC:9659]"}, {"versioned_ensembl_gene_id":"ENSG00000134644.15","gene_symbol":"PUM1","gene_name":"pumilio RNA binding family member 1 [Source:HGNC Symbol;Acc:HGNC:14957]","synonyms":"PUMH1,KIAA0099","biotype":"protein_coding","ncbi_id":"9698","summary":"This gene encodes a member of the PUF family, evolutionarily conserved RNA-binding proteins related to the Pumilio proteins of Drosophila and the fem-3 mRNA binding factor proteins of C. elegans. The encoded protein contains a sequence-specific RNA binding domain comprised of eight repeats and N- and C-terminal flanking regions, and serves as a translational regulator of specific mRNAs by binding to their 3' untranslated regions. The evolutionarily conserved function of the encoded protein in invertebrates and lower vertebrates suggests that the human protein may be involved in translational regulation of embryogenesis, and cell development and differentiation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":30931506,"end":31065991,"strand":-1,"description":"pumilio RNA binding family member 1 [Source:HGNC Symbol;Acc:HGNC:14957]"}, {"versioned_ensembl_gene_id":"ENSG00000274646.4","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201241,"end":54249371,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000164266.10","gene_symbol":"SPINK1","gene_name":"serine peptidase inhibitor, Kazal type 1 [Source:HGNC Symbol;Acc:HGNC:11244]","synonyms":"TATI,Spink3,PSTI,PCTT","biotype":"protein_coding","ncbi_id":"6690","summary":"The protein encoded by this gene is a trypsin inhibitor, which is secreted from pancreatic acinar cells into pancreatic juice. It is thought to function in the prevention of trypsin-catalyzed premature activation of zymogens within the pancreas and the pancreatic duct. Mutations in this gene are associated with hereditary pancreatitis and tropical calcific pancreatitis. [provided by RefSeq, Oct 2008]","start":147824568,"end":147831786,"strand":-1,"description":"serine peptidase inhibitor, Kazal type 1 [Source:HGNC Symbol;Acc:HGNC:11244]"}, {"versioned_ensembl_gene_id":"ENSG00000130338.12","gene_symbol":"TULP4","gene_name":"tubby like protein 4 [Source:HGNC Symbol;Acc:HGNC:15530]","synonyms":"TUSP,KIAA1397","biotype":"protein_coding","ncbi_id":"56995","summary":null,"start":158232236,"end":158511828,"strand":1,"description":"tubby like protein 4 [Source:HGNC Symbol;Acc:HGNC:15530]"}, {"versioned_ensembl_gene_id":"ENSG00000271455.1","gene_symbol":"AC112187.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50603229,"end":50603511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242439.1","gene_symbol":"AC127024.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30830901,"end":30831318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228255.1","gene_symbol":"AC096639.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":213731416,"end":213794587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253628.1","gene_symbol":"AC110011.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":172816621,"end":172819958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213386.3","gene_symbol":"AC022217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172762521,"end":172763258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223773.7","gene_symbol":"CD99P1","gene_name":"CD99 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7083]","synonyms":"NCRNA00103,MIC2R,CXYorf12,CD99L1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401577","summary":null,"start":2609348,"end":2657229,"strand":1,"description":"CD99 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7083]"}, {"versioned_ensembl_gene_id":"ENSG00000213865.7","gene_symbol":"C8orf44","gene_name":"chromosome 8 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:25646]","synonyms":"FLJ11267","biotype":"protein_coding","ncbi_id":"56260","summary":null,"start":66667615,"end":66685564,"strand":1,"description":"chromosome 8 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:25646]"}, {"versioned_ensembl_gene_id":"ENSG00000261596.2","gene_symbol":"AC005632.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21626742,"end":21627569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213005.3","gene_symbol":"PTTG3P","gene_name":"pituitary tumor-transforming 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:13422]","synonyms":"PTTG3","biotype":"processed_pseudogene","ncbi_id":"26255","summary":null,"start":66767400,"end":66768005,"strand":-1,"description":"pituitary tumor-transforming 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:13422]"}, {"versioned_ensembl_gene_id":"ENSG00000120129.5","gene_symbol":"DUSP1","gene_name":"dual specificity phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3064]","synonyms":"MKP-1,HVH1,CL100,PTPN10","biotype":"protein_coding","ncbi_id":"1843","summary":"The protein encoded by this gene is a phosphatase with dual specificity for tyrosine and threonine. The encoded protein can dephosphorylate MAP kinase MAPK1/ERK2, which results in its involvement in several cellular processes. This protein appears to play an important role in the human cellular response to environmental stress as well as in the negative regulation of cellular proliferation. Finally, the encoded protein can make some solid tumors resistant to both chemotherapy and radiotherapy, making it a target for cancer therapy. [provided by RefSeq, Aug 2017]","start":172768090,"end":172771195,"strand":-1,"description":"dual specificity phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:3064]"}, {"versioned_ensembl_gene_id":"ENSG00000253295.1","gene_symbol":"AC022217.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172758226,"end":172762556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278967.1","gene_symbol":"AL138847.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":62607766,"end":62609584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145244.11","gene_symbol":"CORIN","gene_name":"corin, serine peptidase [Source:HGNC Symbol;Acc:HGNC:19012]","synonyms":"TMPRSS10,PRSC,Lrp4,CRN,ATC2","biotype":"protein_coding","ncbi_id":"10699","summary":"This gene encodes a member of the type II transmembrane serine protease class of the trypsin superfamily. Members of this family are composed of multiple structurally distinct domains. The encoded protein converts pro-atrial natriuretic peptide to biologically active atrial natriuretic peptide, a cardiac hormone that regulates blood volume and pressure. This protein may also function as a pro-brain-type natriuretic peptide convertase. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]","start":47593998,"end":47838106,"strand":-1,"description":"corin, serine peptidase [Source:HGNC Symbol;Acc:HGNC:19012]"}, {"versioned_ensembl_gene_id":"ENSG00000260090.1","gene_symbol":"AC092435.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147005492,"end":147009145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237052.7","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"C6orf9,G18.1a,G18.2,AGS4,G18,G18.1b,NG1","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32257772,"end":32262529,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000249617.1","gene_symbol":"AC106872.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165045969,"end":165046280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225263.1","gene_symbol":"PCDH9-AS3","gene_name":"PCDH9 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40427]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874086","summary":null,"start":66977432,"end":66985776,"strand":1,"description":"PCDH9 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40427]"}, {"versioned_ensembl_gene_id":"ENSG00000122692.8","gene_symbol":"SMU1","gene_name":"DNA replication regulator and spliceosomal factor [Source:HGNC Symbol;Acc:HGNC:18247]","synonyms":"SMU-1,fSAP57,FLJ10805,BWD","biotype":"protein_coding","ncbi_id":"55234","summary":null,"start":33041764,"end":33076659,"strand":-1,"description":"DNA replication regulator and spliceosomal factor [Source:HGNC Symbol;Acc:HGNC:18247]"}, {"versioned_ensembl_gene_id":"ENSG00000229897.2","gene_symbol":"SEPT7P7","gene_name":"septin 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130564","summary":null,"start":98606833,"end":98608133,"strand":1,"description":"septin 7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38043]"}, {"versioned_ensembl_gene_id":"ENSG00000248336.1","gene_symbol":"HMGN1P11","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644534","summary":null,"start":62510469,"end":62510771,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39355]"}, {"versioned_ensembl_gene_id":"ENSG00000164251.4","gene_symbol":"F2RL1","gene_name":"F2R like trypsin receptor 1 [Source:HGNC Symbol;Acc:HGNC:3538]","synonyms":"PAR2,GPR11","biotype":"protein_coding","ncbi_id":"2150","summary":"This gene encodes a member of the G-protein coupled receptor 1 family of proteins. The encoded cell surface receptor is activated through proteolytic cleavage of its extracellular amino terminus, resulting in a new amino terminus that acts as a tethered ligand that binds to an extracellular loop domain. Activation of the receptor has been shown to stimulate vascular smooth muscle relaxation, dilate blood vessels, increase blood flow, and lower blood pressure. This protein is also important in the inflammatory response, as well as innate and adaptive immunity. [provided by RefSeq, Jun 2016]","start":76818933,"end":76835315,"strand":1,"description":"F2R like trypsin receptor 1 [Source:HGNC Symbol;Acc:HGNC:3538]"}, {"versioned_ensembl_gene_id":"ENSG00000268366.1","gene_symbol":"AC010271.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40443436,"end":40444087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231434.1","gene_symbol":"AL365440.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158523672,"end":158525838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188419.13","gene_symbol":"CHM","gene_name":"CHM, Rab escort protein 1 [Source:HGNC Symbol;Acc:HGNC:1940]","synonyms":"DXS540,TCD,REP-1","biotype":"protein_coding","ncbi_id":"1121","summary":"This gene encodes component A of the RAB geranylgeranyl transferase holoenzyme. In the dimeric holoenzyme, this subunit binds unprenylated Rab GTPases and then presents them to the catalytic Rab GGTase subunit for the geranylgeranyl transfer reaction. Rab GTPases need to be geranylgeranyled on either one or two cysteine residues in their C-terminus to localize to the correct intracellular membrane. Mutations in this gene are a cause of choroideremia; also known as tapetochoroidal dystrophy (TCD). This X-linked disease is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]","start":85861180,"end":86047562,"strand":-1,"description":"CHM, Rab escort protein 1 [Source:HGNC Symbol;Acc:HGNC:1940]"}, {"versioned_ensembl_gene_id":"ENSG00000251118.1","gene_symbol":"AC008549.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115770586,"end":115770989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160588.9","gene_symbol":"MPZL3","gene_name":"myelin protein zero like 3 [Source:HGNC Symbol;Acc:HGNC:27279]","synonyms":null,"biotype":"protein_coding","ncbi_id":"196264","summary":null,"start":118226690,"end":118252350,"strand":-1,"description":"myelin protein zero like 3 [Source:HGNC Symbol;Acc:HGNC:27279]"}, {"versioned_ensembl_gene_id":"ENSG00000240121.1","gene_symbol":"RPS27P20","gene_name":"ribosomal protein S27 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271581","summary":null,"start":129537869,"end":129538114,"strand":1,"description":"ribosomal protein S27 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36333]"}, {"versioned_ensembl_gene_id":"ENSG00000241476.8","gene_symbol":"SSX2","gene_name":"SSX family member 2 [Source:HGNC Symbol;Acc:HGNC:11336]","synonyms":"SSX,MGC3884,MGC15364,MGC119055,HOM-MEL-40,HD21,CT5.2a","biotype":"protein_coding","ncbi_id":"6757","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX1 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. This gene also has an identical duplicate, GeneID: 727837, located about 45 kb downstream in the opposite orientation on chromosome X. [provided by RefSeq, Jul 2013]","start":52696896,"end":52707189,"strand":-1,"description":"SSX family member 2 [Source:HGNC Symbol;Acc:HGNC:11336]"}, {"versioned_ensembl_gene_id":"ENSG00000062194.15","gene_symbol":"GPBP1","gene_name":"GC-rich promoter binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29520]","synonyms":"vasculin,DKFZp761C169","biotype":"protein_coding","ncbi_id":"65056","summary":"This gene was originally isolated by subtractive hybridization of cDNAs expressed in atherosclerotic plaques with a thrombus, and was found to be expressed only in vascular smooth muscle cells. However, a shorter splice variant was found to be more ubiquitously expressed. This protein is suggested to play a role in the development of atherosclerosis. Studies in mice suggest that it may also function as a GC-rich promoter-specific trans-activating transcription factor. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":57173948,"end":57264679,"strand":1,"description":"GC-rich promoter binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29520]"}, {"versioned_ensembl_gene_id":"ENSG00000121690.10","gene_symbol":"DEPDC7","gene_name":"DEP domain containing 7 [Source:HGNC Symbol;Acc:HGNC:29899]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91614","summary":null,"start":33015864,"end":33033582,"strand":1,"description":"DEP domain containing 7 [Source:HGNC Symbol;Acc:HGNC:29899]"}, {"versioned_ensembl_gene_id":"ENSG00000104093.13","gene_symbol":"DMXL2","gene_name":"Dmx like 2 [Source:HGNC Symbol;Acc:HGNC:2938]","synonyms":"RC3,KIAA0856","biotype":"protein_coding","ncbi_id":"23312","summary":"This gene encodes a protein with 12 WD domains. Proteins with WD domains are involved in many functions including participation in signal transduction pathways. Participation of the encoded protein in regulation of the Notch signaling pathway has been demonstrated in vitro using several human cell lines (PMID:20810660). A gene encoding a similar protein is located on chromosome 5. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":51447711,"end":51622833,"strand":-1,"description":"Dmx like 2 [Source:HGNC Symbol;Acc:HGNC:2938]"}, {"versioned_ensembl_gene_id":"ENSG00000167747.14","gene_symbol":"C19orf48","gene_name":"chromosome 19 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:29667]","synonyms":"MGC13170,BC006151","biotype":"protein_coding","ncbi_id":"84798","summary":null,"start":50797704,"end":50804929,"strand":-1,"description":"chromosome 19 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:29667]"}, {"versioned_ensembl_gene_id":"ENSG00000226432.3","gene_symbol":"AC010342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24170370,"end":24171246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229124.6","gene_symbol":"VIM-AS1","gene_name":"VIM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44879]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507347","summary":null,"start":17214239,"end":17229985,"strand":-1,"description":"VIM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44879]"}, {"versioned_ensembl_gene_id":"ENSG00000271609.1","gene_symbol":"AC005632.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21538487,"end":21538794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257639.1","gene_symbol":"AC005632.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21532945,"end":21550373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256955.2","gene_symbol":"AC131009.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131857420,"end":131864538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237742.6","gene_symbol":"AL365259.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125578558,"end":125749190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226409.2","gene_symbol":"AL450332.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125370034,"end":125445183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258772.1","gene_symbol":"AL355922.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20916766,"end":20928580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280254.1","gene_symbol":"AC233723.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4787057,"end":4789162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259407.1","gene_symbol":"AC021739.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85744109,"end":85750281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259544.1","gene_symbol":"AC021739.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85726115,"end":85727227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230505.4","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439377,"end":29441048,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000101343.14","gene_symbol":"CRNKL1","gene_name":"crooked neck pre-mRNA splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:15762]","synonyms":"SYF3,CRN,Clf1,CLF","biotype":"protein_coding","ncbi_id":"51340","summary":"The crooked neck (crn) gene of Drosophila is essential for embryogenesis and is thought to be involved in cell cycle progression and pre-mRNA splicing. A protein encoded by this human locus has been found to localize to pre-mRNA splicing complexes in the nucleus and is necessary for pre-mRNA splicing. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2013]","start":20034368,"end":20056046,"strand":-1,"description":"crooked neck pre-mRNA splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:15762]"}, {"versioned_ensembl_gene_id":"ENSG00000233576.1","gene_symbol":"AC131235.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":184076779,"end":184084219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227835.8","gene_symbol":"CARM1P1","gene_name":"coactivator associated arginine methyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23392]","synonyms":"CARM1L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100130873","summary":null,"start":2907073,"end":3053408,"strand":-1,"description":"coactivator associated arginine methyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23392]"}, {"versioned_ensembl_gene_id":"ENSG00000183559.11","gene_symbol":"C10orf120","gene_name":"chromosome 10 open reading frame 120 [Source:HGNC Symbol;Acc:HGNC:25707]","synonyms":"bA318C4.1","biotype":"protein_coding","ncbi_id":"399814","summary":null,"start":122697709,"end":122699822,"strand":-1,"description":"chromosome 10 open reading frame 120 [Source:HGNC Symbol;Acc:HGNC:25707]"}, {"versioned_ensembl_gene_id":"ENSG00000223400.1","gene_symbol":"AP006748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41576135,"end":41581319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237690.1","gene_symbol":"CR936918.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29290770,"end":29291712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248847.2","gene_symbol":"AC074087.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62489495,"end":62490218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181856.14","gene_symbol":"SLC2A4","gene_name":"solute carrier family 2 member 4 [Source:HGNC Symbol;Acc:HGNC:11009]","synonyms":"GLUT4","biotype":"protein_coding","ncbi_id":"6517","summary":"This gene is a member of the solute carrier family 2 (facilitated glucose transporter) family and encodes a protein that functions as an insulin-regulated facilitative glucose transporter. In the absence of insulin, this integral membrane protein is sequestered within the cells of muscle and adipose tissue. Within minutes of insulin stimulation, the protein moves to the cell surface and begins to transport glucose across the cell membrane. Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM). [provided by RefSeq, Jul 2008]","start":7281667,"end":7288257,"strand":1,"description":"solute carrier family 2 member 4 [Source:HGNC Symbol;Acc:HGNC:11009]"}, {"versioned_ensembl_gene_id":"ENSG00000250507.1","gene_symbol":"AC245884.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54328272,"end":54331434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267513.3","gene_symbol":"HMGN1P31","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728111","summary":null,"start":60794613,"end":60794916,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39375]"}, {"versioned_ensembl_gene_id":"ENSG00000267382.1","gene_symbol":"AC010928.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60611773,"end":60654623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205396.11","gene_symbol":"LINC00661","gene_name":"long intergenic non-protein coding RNA 661 [Source:HGNC Symbol;Acc:HGNC:27002]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"126536","summary":null,"start":16015287,"end":16027462,"strand":1,"description":"long intergenic non-protein coding RNA 661 [Source:HGNC Symbol;Acc:HGNC:27002]"}, {"versioned_ensembl_gene_id":"ENSG00000275618.2","gene_symbol":"BFAR","gene_name":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]","synonyms":"RNF47,BAR","biotype":"protein_coding","ncbi_id":"51283","summary":null,"start":14632814,"end":14669237,"strand":1,"description":"bifunctional apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:17613]"}, {"versioned_ensembl_gene_id":"ENSG00000276474.1","gene_symbol":"AC231759.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52326166,"end":52326762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102384.13","gene_symbol":"CENPI","gene_name":"centromere protein I [Source:HGNC Symbol;Acc:HGNC:3968]","synonyms":"Mis6,LRPR1,FSHPRH1,CENP-I","biotype":"protein_coding","ncbi_id":"2491","summary":"This gene encodes a centromere protein that is a component of the CENPA-NAC (nucleosome-associated) complex. This complex is critical for accurate chromosome alignment and segregation and it ensures proper mitotic progression. This protein regulates the recruitment of kinetochore-associated proteins that are required to generate the spindle checkpoint signal. The product of this gene is involved in the response of gonadal tissues to follicle-stimulating hormone. Mutations in this gene may be involved in human X-linked disorders of gonadal development and gametogenesis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 13. [provided by RefSeq, Jan 2016]","start":101098218,"end":101163681,"strand":1,"description":"centromere protein I [Source:HGNC Symbol;Acc:HGNC:3968]"}, {"versioned_ensembl_gene_id":"ENSG00000282241.1","gene_symbol":"AL121839.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":91756515,"end":91763457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282153.1","gene_symbol":"AL121839.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91712770,"end":91714276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123307.3","gene_symbol":"NEUROD4","gene_name":"neuronal differentiation 4 [Source:HGNC Symbol;Acc:HGNC:13802]","synonyms":"MATH-3,bHLHa4,Atoh3,ATH-3","biotype":"protein_coding","ncbi_id":"58158","summary":null,"start":55019945,"end":55030014,"strand":1,"description":"neuronal differentiation 4 [Source:HGNC Symbol;Acc:HGNC:13802]"}, {"versioned_ensembl_gene_id":"ENSG00000261319.1","gene_symbol":"LINC02152","gene_name":"long intergenic non-protein coding RNA 2152 [Source:HGNC Symbol;Acc:HGNC:53014]","synonyms":"ENST00000566208","biotype":"lincRNA","ncbi_id":"105371071","summary":null,"start":8298492,"end":8299772,"strand":1,"description":"long intergenic non-protein coding RNA 2152 [Source:HGNC Symbol;Acc:HGNC:53014]"}, {"versioned_ensembl_gene_id":"ENSG00000248329.5","gene_symbol":"APELA","gene_name":"apelin receptor early endogenous ligand [Source:HGNC Symbol;Acc:HGNC:48925]","synonyms":"tdl,Ende,ELA","biotype":"protein_coding","ncbi_id":"100506013","summary":"This gene encodes a peptide hormone that binds to the Apelin receptor. The encoded protein is required for heart development in zebrafish and has been shown to maintain self-renewal of human embryonic stem cells through activation of the PI3K/AKT pathway. Experiments in human and mouse cell lines point to additional roles for the encoded protein in angiogenesis and regulation of vascular tone. [provided by RefSeq, Jul 2016]","start":164877004,"end":164898965,"strand":1,"description":"apelin receptor early endogenous ligand [Source:HGNC Symbol;Acc:HGNC:48925]"}, {"versioned_ensembl_gene_id":"ENSG00000255240.5","gene_symbol":"AP001636.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58933643,"end":59058659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236452.1","gene_symbol":"AC123023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34203244,"end":34268811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226320.5","gene_symbol":"LINC01811","gene_name":"long intergenic non-protein coding RNA 1811 [Source:HGNC Symbol;Acc:HGNC:52615]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928114","summary":null,"start":34159334,"end":34562877,"strand":1,"description":"long intergenic non-protein coding RNA 1811 [Source:HGNC Symbol;Acc:HGNC:52615]"}, {"versioned_ensembl_gene_id":"ENSG00000170523.3","gene_symbol":"KRT83","gene_name":"keratin 83 [Source:HGNC Symbol;Acc:HGNC:6460]","synonyms":"KRTHB3,Hb-3","biotype":"protein_coding","ncbi_id":"3889","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB1 and KRTHB6, is found primarily in the hair cortex. [provided by RefSeq, Jul 2008]","start":52314301,"end":52321398,"strand":-1,"description":"keratin 83 [Source:HGNC Symbol;Acc:HGNC:6460]"}, {"versioned_ensembl_gene_id":"ENSG00000249746.1","gene_symbol":"AC099509.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96213346,"end":96215075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280216.1","gene_symbol":"AL022326.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":39379610,"end":39380015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229400.1","gene_symbol":"AL596330.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":224717504,"end":224730662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230304.1","gene_symbol":"CICP6","gene_name":"capicua transcriptional repressor pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37755]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507251","summary":null,"start":198223497,"end":198226310,"strand":-1,"description":"capicua transcriptional repressor pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37755]"}, {"versioned_ensembl_gene_id":"ENSG00000226008.1","gene_symbol":"SEPT14P3","gene_name":"septin 14 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51687]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107105265","summary":null,"start":198228194,"end":198228376,"strand":1,"description":"septin 14 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51687]"}, {"versioned_ensembl_gene_id":"ENSG00000283582.1","gene_symbol":"AC007671.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":22116629,"end":22134851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256714.1","gene_symbol":"AC087318.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22395088,"end":22398075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227830.1","gene_symbol":"TRIM60P3Y","gene_name":"tripartite motif containing 60 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:38409]","synonyms":"TRIM60PY3,TRIM60P3","biotype":"processed_pseudogene","ncbi_id":"100420364","summary":null,"start":8413037,"end":8414054,"strand":-1,"description":"tripartite motif containing 60 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:38409]"}, {"versioned_ensembl_gene_id":"ENSG00000095380.10","gene_symbol":"NANS","gene_name":"N-acetylneuraminate synthase [Source:HGNC Symbol;Acc:HGNC:19237]","synonyms":"SAS","biotype":"protein_coding","ncbi_id":"54187","summary":"This gene encodes an enzyme that functions in the biosynthetic pathways of sialic acids. In vitro, the encoded protein uses N-acetylmannosamine 6-phosphate and mannose 6-phosphate as substrates to generate phosphorylated forms of N-acetylneuraminic acid (Neu5Ac) and 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid (KDN), respectively; however, it exhibits much higher activity toward the Neu5Ac phosphate product. In insect cells, expression of this gene results in Neu5Ac and KDN production. This gene is related to the E. coli sialic acid synthase gene neuB, and it can partially restore sialic acid synthase activity in an E. coli neuB-negative mutant. [provided by RefSeq, Jul 2008]","start":98056739,"end":98083075,"strand":1,"description":"N-acetylneuraminate synthase [Source:HGNC Symbol;Acc:HGNC:19237]"}, {"versioned_ensembl_gene_id":"ENSG00000232963.1","gene_symbol":"HMGN2P20","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39385]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646049","summary":null,"start":24330402,"end":24330674,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39385]"}, {"versioned_ensembl_gene_id":"ENSG00000250565.6","gene_symbol":"ATP6V1E2","gene_name":"ATPase H+ transporting V1 subunit E2 [Source:HGNC Symbol;Acc:HGNC:18125]","synonyms":"VMA4,MGC9341,ATP6V1EL2,ATP6EL2,ATP6E1","biotype":"protein_coding","ncbi_id":"90423","summary":null,"start":46490750,"end":46542557,"strand":-1,"description":"ATPase H+ transporting V1 subunit E2 [Source:HGNC Symbol;Acc:HGNC:18125]"}, {"versioned_ensembl_gene_id":"ENSG00000166311.9","gene_symbol":"SMPD1","gene_name":"sphingomyelin phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:11120]","synonyms":"ASM","biotype":"protein_coding","ncbi_id":"6609","summary":"The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2010]","start":6390431,"end":6394998,"strand":1,"description":"sphingomyelin phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:11120]"}, {"versioned_ensembl_gene_id":"ENSG00000237033.2","gene_symbol":"CASP3P1","gene_name":"caspase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131616","summary":null,"start":70660657,"end":70661265,"strand":-1,"description":"caspase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43596]"}, {"versioned_ensembl_gene_id":"ENSG00000233656.1","gene_symbol":"AL445430.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11417350,"end":11481239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226920.1","gene_symbol":"AL160004.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":229440284,"end":229441020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151650.7","gene_symbol":"VENTX","gene_name":"VENT homeobox [Source:HGNC Symbol;Acc:HGNC:13639]","synonyms":"VENTX2,HPX42B","biotype":"protein_coding","ncbi_id":"27287","summary":"This gene encodes a member of the Vent family of homeodomain proteins. The encoded protein may function as a transcriptional repressor and be involved in mesodermal patterning and hemopoietic stem cell maintenance. Multiple pseudogenes exist for this gene. A transcribed pseudogene located on chromosome X may lead to antigen production in certain melanomas. [provided by RefSeq, Jul 2008]","start":133237404,"end":133241929,"strand":1,"description":"VENT homeobox [Source:HGNC Symbol;Acc:HGNC:13639]"}, {"versioned_ensembl_gene_id":"ENSG00000203416.3","gene_symbol":"FAM32BP","gene_name":"family with sequence similarity 32 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30945]","synonyms":"FAM32B","biotype":"processed_pseudogene","ncbi_id":"399656","summary":null,"start":17213516,"end":17214155,"strand":1,"description":"family with sequence similarity 32 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30945]"}, {"versioned_ensembl_gene_id":"ENSG00000248801.6","gene_symbol":"C8orf34-AS1","gene_name":"C8orf34 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27840]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"286189","summary":null,"start":68303468,"end":68331491,"strand":-1,"description":"C8orf34 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27840]"}, {"versioned_ensembl_gene_id":"ENSG00000132259.12","gene_symbol":"CNGA4","gene_name":"cyclic nucleotide gated channel alpha 4 [Source:HGNC Symbol;Acc:HGNC:2152]","synonyms":"OCNCb,OCNC2,CNGB2,CNG5,CNCA2","biotype":"protein_coding","ncbi_id":"1262","summary":"CNGA4 is a modulatory subunit of vertebrate cyclic nucleotide-gated membrane channels that transduce odorant signals (Munger et al., 2001 [PubMed 11739959]).[supplied by OMIM, Mar 2008]","start":6234765,"end":6244429,"strand":1,"description":"cyclic nucleotide gated channel alpha 4 [Source:HGNC Symbol;Acc:HGNC:2152]"}, {"versioned_ensembl_gene_id":"ENSG00000266488.2","gene_symbol":"AC226154.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11859673,"end":11893500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172772.3","gene_symbol":"OR10W1","gene_name":"olfactory receptor family 10 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:15139]","synonyms":"OR10W1P","biotype":"protein_coding","ncbi_id":"81341","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58266792,"end":58268260,"strand":-1,"description":"olfactory receptor family 10 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:15139]"}, {"versioned_ensembl_gene_id":"ENSG00000166535.19","gene_symbol":"A2ML1","gene_name":"alpha-2-macroglobulin like 1 [Source:HGNC Symbol;Acc:HGNC:23336]","synonyms":"p170,FLJ25179,CPAMD9","biotype":"protein_coding","ncbi_id":"144568","summary":"This gene encodes a member of the alpha-macroglobulin superfamily. The encoded protein is thought to be an N-glycosylated monomeric protein that acts as an inhibitor of several proteases. It has been shown to form covalent interactions with proteases, and has been reported as the p170 antigen recognized by autoantibodies in the autoimmune disease paraneoplastic pemphigus (PNP; PMID:20805888). Mutations in these gene have also been associated with some cases of Noonan syndrome (NS; PMID:24939586) as well as some cases of otitis media (PMID:26121085). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":8822472,"end":8887001,"strand":1,"description":"alpha-2-macroglobulin like 1 [Source:HGNC Symbol;Acc:HGNC:23336]"}, {"versioned_ensembl_gene_id":"ENSG00000267618.5","gene_symbol":"AC004223.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35011349,"end":35121493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250351.1","gene_symbol":"AC233724.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17620533,"end":17620939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089094.18","gene_symbol":"KDM2B","gene_name":"lysine demethylase 2B [Source:HGNC Symbol;Acc:HGNC:13610]","synonyms":"CXXC2,PCCX2,JHDM1B,FBXL10,Fbl10","biotype":"protein_coding","ncbi_id":"84678","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":121429097,"end":121581015,"strand":-1,"description":"lysine demethylase 2B [Source:HGNC Symbol;Acc:HGNC:13610]"}, {"versioned_ensembl_gene_id":"ENSG00000271296.1","gene_symbol":"AC233724.14","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17614781,"end":17615111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244476.2","gene_symbol":"ERVFRD-1","gene_name":"endogenous retrovirus group FRD member 1, envelope [Source:HGNC Symbol;Acc:HGNC:33823]","synonyms":"syncytin-2,HERV-W/FRD,HERV-FRD,ERVFRDE1,envFRD","biotype":"protein_coding","ncbi_id":"405754","summary":"Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of a human endogenous retrovirus provirus on chromosome 6 that has inactivating mutations in the gag and pol genes. This gene is the envelope glycoprotein gene which appears to have been selectively preserved. The gene's protein product plays a major role in placental development and trophoblast fusion. The protein has the characteristics of a typical retroviral envelope protein, including a cleavage site that separates the surface (SU) and transmembrane (TM) proteins which form a heterodimer. [provided by RefSeq, Jun 2012]","start":11102489,"end":11111732,"strand":-1,"description":"endogenous retrovirus group FRD member 1, envelope [Source:HGNC Symbol;Acc:HGNC:33823]"}, {"versioned_ensembl_gene_id":"ENSG00000166529.14","gene_symbol":"ZSCAN21","gene_name":"zinc finger and SCAN domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13104]","synonyms":"ZNF38,Zipro1,NY-REN-21,DKFZp434L134","biotype":"protein_coding","ncbi_id":"7589","summary":null,"start":100049774,"end":100065038,"strand":1,"description":"zinc finger and SCAN domain containing 21 [Source:HGNC Symbol;Acc:HGNC:13104]"}, {"versioned_ensembl_gene_id":"ENSG00000254589.1","gene_symbol":"EIF4A2P3","gene_name":"eukaryotic translation initiation factor 4A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133309","summary":null,"start":58242043,"end":58243097,"strand":-1,"description":"eukaryotic translation initiation factor 4A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45100]"}, {"versioned_ensembl_gene_id":"ENSG00000135968.20","gene_symbol":"GCC2","gene_name":"GRIP and coiled-coil domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23218]","synonyms":"KIAA0336,GCC185","biotype":"protein_coding","ncbi_id":"9648","summary":"The protein encoded by this gene is a peripheral membrane protein localized to the trans-Golgi network. It is sensitive to brefeldin A. This encoded protein contains a GRIP domain which is thought to be used in targeting. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":108448561,"end":108509415,"strand":1,"description":"GRIP and coiled-coil domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23218]"}, {"versioned_ensembl_gene_id":"ENSG00000119636.15","gene_symbol":"BBOF1","gene_name":"basal body orientation factor 1 [Source:HGNC Symbol;Acc:HGNC:19855]","synonyms":"CCDC176,C14orf45","biotype":"protein_coding","ncbi_id":"80127","summary":null,"start":74019353,"end":74082863,"strand":1,"description":"basal body orientation factor 1 [Source:HGNC Symbol;Acc:HGNC:19855]"}, {"versioned_ensembl_gene_id":"ENSG00000156860.15","gene_symbol":"FBRS","gene_name":"fibrosin [Source:HGNC Symbol;Acc:HGNC:20442]","synonyms":"FLJ11618,FBS1,FBS","biotype":"protein_coding","ncbi_id":"64319","summary":"Fibrosin is a lymphokine secreted by activated lymphocytes that induces fibroblast proliferation (Prakash and Robbins, 1998 [PubMed 9809749]).[supplied by OMIM, Mar 2008]","start":30658431,"end":30670814,"strand":1,"description":"fibrosin [Source:HGNC Symbol;Acc:HGNC:20442]"}, {"versioned_ensembl_gene_id":"ENSG00000229259.1","gene_symbol":"LRRC37A12P","gene_name":"leucine rich repeat containing 37 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:43816]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101929254","summary":null,"start":32423214,"end":32426789,"strand":-1,"description":"leucine rich repeat containing 37 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:43816]"}, {"versioned_ensembl_gene_id":"ENSG00000249282.1","gene_symbol":"AC233724.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17601882,"end":17602134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268107.5","gene_symbol":"AC003005.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57487718,"end":57505381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230818.1","gene_symbol":"MTND2P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873347","summary":null,"start":19747823,"end":19748621,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42117]"}, {"versioned_ensembl_gene_id":"ENSG00000254091.2","gene_symbol":"AC022784.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9233013,"end":9233449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171936.2","gene_symbol":"OR10H3","gene_name":"olfactory receptor family 10 subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:8174]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26532","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15737985,"end":15742343,"strand":1,"description":"olfactory receptor family 10 subfamily H member 3 [Source:HGNC Symbol;Acc:HGNC:8174]"}, {"versioned_ensembl_gene_id":"ENSG00000226826.10","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33216374,"end":33227649,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000258891.1","gene_symbol":"AC005480.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73896164,"end":73938114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231916.1","gene_symbol":"AC006033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38311383,"end":38311808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179403.11","gene_symbol":"VWA1","gene_name":"von Willebrand factor A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30910]","synonyms":"WARP,VWA-1,FLJ22215","biotype":"protein_coding","ncbi_id":"64856","summary":"VWA1 belongs to the von Willebrand factor (VWF; MIM 613160) A (VWFA) domain superfamily of extracellular matrix proteins and appears to play a role in cartilage structure and function (Fitzgerald et al., 2002 [PubMed 12062410]).[supplied by OMIM, Nov 2010]","start":1434861,"end":1442882,"strand":1,"description":"von Willebrand factor A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30910]"}, {"versioned_ensembl_gene_id":"ENSG00000214100.8","gene_symbol":"PLAC9P1","gene_name":"placenta specific 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52678]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"389033","summary":null,"start":129922863,"end":129934317,"strand":-1,"description":"placenta specific 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52678]"}, {"versioned_ensembl_gene_id":"ENSG00000104219.12","gene_symbol":"ZDHHC2","gene_name":"zinc finger DHHC-type containing 2 [Source:HGNC Symbol;Acc:HGNC:18469]","synonyms":"ZNF372,DHHC2","biotype":"protein_coding","ncbi_id":"51201","summary":null,"start":17156029,"end":17224799,"strand":1,"description":"zinc finger DHHC-type containing 2 [Source:HGNC Symbol;Acc:HGNC:18469]"}, {"versioned_ensembl_gene_id":"ENSG00000233428.1","gene_symbol":"AC019050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129496297,"end":129496788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254598.2","gene_symbol":"CSNK2A3","gene_name":"casein kinase 2 alpha 3 [Source:HGNC Symbol;Acc:HGNC:2458]","synonyms":"CSNK2A1P","biotype":"protein_coding","ncbi_id":"283106","summary":"This gene encodes a protein that is highly similar to the casein kinase II alpha protein. Casein kinase II is a serine/threonine protein kinase complex that phosphorylates numerous substrates including casein. The alpha subunit is the catalytic component of the complex. Mutations in this gene may be associated with a susceptibility to lung cancer. There are contradictory views among published reports of this gene as to whether or not it is a protein-coding gene or a processed pseudogene (PMIDs: 20625391, 20625391 and 10094393). [provided by RefSeq, Feb 2012]","start":11351942,"end":11353357,"strand":-1,"description":"casein kinase 2 alpha 3 [Source:HGNC Symbol;Acc:HGNC:2458]"}, {"versioned_ensembl_gene_id":"ENSG00000235698.1","gene_symbol":"PA2G4P2","gene_name":"proliferation-associated 2G4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16531]","synonyms":"PA2G4L5,bA102J14.2","biotype":"processed_pseudogene","ncbi_id":"170533","summary":null,"start":12380056,"end":12381255,"strand":1,"description":"proliferation-associated 2G4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16531]"}, {"versioned_ensembl_gene_id":"ENSG00000234356.1","gene_symbol":"AC009945.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10476581,"end":10476878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236414.1","gene_symbol":"AC004415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10702676,"end":10707406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279437.1","gene_symbol":"Z82170.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":83506023,"end":83509214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244705.1","gene_symbol":"AC020658.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40312352,"end":40313289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216740.2","gene_symbol":"ANXA2P3","gene_name":"annexin A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:540]","synonyms":"LPC2C,LIP2,ANX2P3,ANX2L3","biotype":"processed_pseudogene","ncbi_id":"305","summary":null,"start":64825572,"end":64826579,"strand":1,"description":"annexin A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:540]"}, {"versioned_ensembl_gene_id":"ENSG00000175318.11","gene_symbol":"GRAMD2A","gene_name":"GRAM domain containing 2A [Source:HGNC Symbol;Acc:HGNC:27287]","synonyms":"GRAMD2","biotype":"protein_coding","ncbi_id":"196996","summary":null,"start":72159807,"end":72197785,"strand":-1,"description":"GRAM domain containing 2A [Source:HGNC Symbol;Acc:HGNC:27287]"}, {"versioned_ensembl_gene_id":"ENSG00000280663.4","gene_symbol":"PCMTD2","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15882]","synonyms":"FLJ10883,C20orf36","biotype":"protein_coding","ncbi_id":"55251","summary":null,"start":64259386,"end":64278487,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15882]"}, {"versioned_ensembl_gene_id":"ENSG00000235240.1","gene_symbol":"AC026185.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11488300,"end":11488473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234463.1","gene_symbol":"COX6CP12","gene_name":"cytochrome c oxidase subunit 6C pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481682","summary":null,"start":68645326,"end":68645527,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49364]"}, {"versioned_ensembl_gene_id":"ENSG00000250850.2","gene_symbol":"AL161781.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37002697,"end":37008040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115128.6","gene_symbol":"SF3B6","gene_name":"splicing factor 3b subunit 6 [Source:HGNC Symbol;Acc:HGNC:30096]","synonyms":"SF3B14a,SAP14a,P14,Ht006,CGI-110","biotype":"protein_coding","ncbi_id":"51639","summary":"This gene encodes a 14 kDa protein subunit of the splicing factor 3b complex. Splicing factor 3b associates with both the U2 and U11/U12 small nuclear ribonucleoprotein complexes (U2 snRNP) of spliceosomes. This 14 kDa protein interacts directly with subunit 1 of the splicing factor 3b complex. This 14 kDa protein also interacts directly with the adenosine that carries out the first transesterification step of splicing at the pre-mRNA branch site. [provided by RefSeq, Jul 2008]","start":24067584,"end":24076443,"strand":-1,"description":"splicing factor 3b subunit 6 [Source:HGNC Symbol;Acc:HGNC:30096]"}, {"versioned_ensembl_gene_id":"ENSG00000277737.3","gene_symbol":"FP325317.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43109866,"end":43125905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224401.2","gene_symbol":"RPL7P57","gene_name":"ribosomal protein L7 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:35901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643507","summary":null,"start":47840963,"end":47841702,"strand":-1,"description":"ribosomal protein L7 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:35901]"}, {"versioned_ensembl_gene_id":"ENSG00000229670.2","gene_symbol":"PKP4P1","gene_name":"plakophilin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42661]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402116","summary":null,"start":209178966,"end":209181123,"strand":1,"description":"plakophilin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42661]"}, {"versioned_ensembl_gene_id":"ENSG00000084444.13","gene_symbol":"FAM234B","gene_name":"family with sequence similarity 234 member B [Source:HGNC Symbol;Acc:HGNC:29288]","synonyms":"KIAA1467","biotype":"protein_coding","ncbi_id":"57613","summary":null,"start":13044284,"end":13142521,"strand":1,"description":"family with sequence similarity 234 member B [Source:HGNC Symbol;Acc:HGNC:29288]"}, {"versioned_ensembl_gene_id":"ENSG00000233968.6","gene_symbol":"AL157895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19710328,"end":19728550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281073.1","gene_symbol":"AC244216.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13264443,"end":13267241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260416.1","gene_symbol":"AL096828.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63127495,"end":63129459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131050.10","gene_symbol":"BPIFA2","gene_name":"BPI fold containing family A member 2 [Source:HGNC Symbol;Acc:HGNC:16203]","synonyms":"SPLUNC2,PSP,C20orf70,bA49G10.1","biotype":"protein_coding","ncbi_id":"140683","summary":"This gene encodes a member of the palate, lung and nasal epithelium clone (Plunc) family of proteins. Members of this family have been proposed to play a role in the local antibacterial response in nose, mouth and upper respiratory pathways. The encoded soluble salivary protein binds bacterial lipopolysaccharide (LPS) and inhibits bacterial growth. This gene is present in a gene cluster on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":33161768,"end":33181412,"strand":1,"description":"BPI fold containing family A member 2 [Source:HGNC Symbol;Acc:HGNC:16203]"}, {"versioned_ensembl_gene_id":"ENSG00000228227.1","gene_symbol":"AL844220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30176301,"end":30178125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233944.1","gene_symbol":"LINC00265-3P","gene_name":"long intergenic non-protein coding RNA 265-3, pseudogene [Source:HGNC Symbol;Acc:HGNC:38536]","synonyms":"NCRNA00265C,NCRNA00265-3P","biotype":"processed_pseudogene","ncbi_id":"100287470","summary":null,"start":25393154,"end":25394056,"strand":-1,"description":"long intergenic non-protein coding RNA 265-3, pseudogene [Source:HGNC Symbol;Acc:HGNC:38536]"}, {"versioned_ensembl_gene_id":"ENSG00000186190.7","gene_symbol":"BPIFB3","gene_name":"BPI fold containing family B member 3 [Source:HGNC Symbol;Acc:HGNC:16178]","synonyms":"RYA3,LPLUNC3,dJ726C3.4,C20orf185","biotype":"protein_coding","ncbi_id":"359710","summary":null,"start":33055424,"end":33073628,"strand":1,"description":"BPI fold containing family B member 3 [Source:HGNC Symbol;Acc:HGNC:16178]"}, {"versioned_ensembl_gene_id":"ENSG00000197696.9","gene_symbol":"NMB","gene_name":"neuromedin B [Source:HGNC Symbol;Acc:HGNC:7842]","synonyms":"MGC3936,MGC2277,MGC17211","biotype":"protein_coding","ncbi_id":"4828","summary":"This gene encodes a member of the bombesin-like family of neuropeptides, which negatively regulate eating behavior. The encoded protein may regulate colonic smooth muscle contraction through binding to its cognate receptor, the neuromedin B receptor (NMBR). Polymorphisms of this gene may be associated with hunger, weight gain and obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":84655129,"end":84658563,"strand":-1,"description":"neuromedin B [Source:HGNC Symbol;Acc:HGNC:7842]"}, {"versioned_ensembl_gene_id":"ENSG00000258066.1","gene_symbol":"AC138331.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77775783,"end":77783576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013583.8","gene_symbol":"HEBP1","gene_name":"heme binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17176]","synonyms":"HEBP,HBP","biotype":"protein_coding","ncbi_id":"50865","summary":"The full-length protein encoded by this gene is an intracellular tetrapyrrole-binding protein. This protein includes a natural chemoattractant peptide of 21 amino acids at the N-terminus, which is a natural ligand for formyl peptide receptor-like receptor 2 (FPRL2) and promotes calcium mobilization and chemotaxis in monocytes and dendritic cells. [provided by RefSeq, Jul 2008]","start":12974864,"end":13000273,"strand":-1,"description":"heme binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17176]"}, {"versioned_ensembl_gene_id":"ENSG00000231615.2","gene_symbol":"AL645568.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173362397,"end":173363733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228086.1","gene_symbol":"AL589990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100462399,"end":100485997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235451.1","gene_symbol":"PNPLA4P1","gene_name":"patatin like phospholipase domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38085]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100462832","summary":null,"start":14081075,"end":14086600,"strand":1,"description":"patatin like phospholipase domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38085]"}, {"versioned_ensembl_gene_id":"ENSG00000176399.3","gene_symbol":"DMRTA1","gene_name":"DMRT like family A1 [Source:HGNC Symbol;Acc:HGNC:13826]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63951","summary":null,"start":22446841,"end":22455740,"strand":1,"description":"DMRT like family A1 [Source:HGNC Symbol;Acc:HGNC:13826]"}, {"versioned_ensembl_gene_id":"ENSG00000236921.1","gene_symbol":"AL157937.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22203990,"end":22214672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152595.16","gene_symbol":"MEPE","gene_name":"matrix extracellular phosphoglycoprotein [Source:HGNC Symbol;Acc:HGNC:13361]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56955","summary":"This gene encodes a secreted calcium-binding phosphoprotein that belongs to the small integrin-binding ligand, N-linked glycoprotein (SIBLING) family of proteins. Members of this family are components of the extracellular matrix of bone and dentin and regulate bone mineralization. Deficiency of a similar protein in mouse results in increased bone mass. Mice lacking this gene are resistant to aging-related trabecular bone loss. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":87821411,"end":87846817,"strand":1,"description":"matrix extracellular phosphoglycoprotein [Source:HGNC Symbol;Acc:HGNC:13361]"}, {"versioned_ensembl_gene_id":"ENSG00000067445.20","gene_symbol":"TRO","gene_name":"trophinin [Source:HGNC Symbol;Acc:HGNC:12326]","synonyms":"MAGED3,MAGE-D3,KIAA1114","biotype":"protein_coding","ncbi_id":"7216","summary":"This gene encodes a membrane protein that mediates cell adhesion between trophoblastic cells and the epithelial cells of the endometrium. The encoded protein participates in cell signalling during embryo implantation, and may also be involved in cancer formation. This gene is located near several other closely related genes on chromosome X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":54920462,"end":54931431,"strand":1,"description":"trophinin [Source:HGNC Symbol;Acc:HGNC:12326]"}, {"versioned_ensembl_gene_id":"ENSG00000168334.8","gene_symbol":"XIRP1","gene_name":"xin actin binding repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:14301]","synonyms":"Xin,DKFZp451D042,CMYA1","biotype":"protein_coding","ncbi_id":"165904","summary":"The protein encoded by this gene is a striated muscle protein and belongs to the Xin actin-binding repeat-containing protein (XIRP) family. The protein functions to protect actin filaments during depolymerization. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2017]","start":39183210,"end":39192596,"strand":-1,"description":"xin actin binding repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:14301]"}, {"versioned_ensembl_gene_id":"ENSG00000153046.17","gene_symbol":"CDYL","gene_name":"chromodomain Y like [Source:HGNC Symbol;Acc:HGNC:1811]","synonyms":"DKFZP586C1622,CDYL1","biotype":"protein_coding","ncbi_id":"9425","summary":"Chromodomain Y is a primate-specific Y-chromosomal gene family expressed exclusively in the testis and implicated in infertility. Although the Y-linked genes are testis-specific, this autosomal gene is ubiquitously expressed. The Y-linked genes arose by retrotransposition of an mRNA from this gene, followed by amplification of the retroposed gene. Proteins encoded by this gene superfamily possess a chromodomain, a motif implicated in chromatin binding and gene suppression, and a catalytic domain believed to be involved in histone acetylation. Multiple proteins are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":4706159,"end":4955551,"strand":1,"description":"chromodomain Y like [Source:HGNC Symbol;Acc:HGNC:1811]"}, {"versioned_ensembl_gene_id":"ENSG00000230983.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31252275,"end":31256445,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000259664.2","gene_symbol":"LINC02254","gene_name":"long intergenic non-protein coding RNA 2254 [Source:HGNC Symbol;Acc:HGNC:53152]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927286","summary":null,"start":97370371,"end":97521811,"strand":-1,"description":"long intergenic non-protein coding RNA 2254 [Source:HGNC Symbol;Acc:HGNC:53152]"}, {"versioned_ensembl_gene_id":"ENSG00000259485.1","gene_symbol":"LINC02253","gene_name":"long intergenic non-protein coding RNA 2253 [Source:HGNC Symbol;Acc:HGNC:53151]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984764","summary":null,"start":97295881,"end":97432094,"strand":1,"description":"long intergenic non-protein coding RNA 2253 [Source:HGNC Symbol;Acc:HGNC:53151]"}, {"versioned_ensembl_gene_id":"ENSG00000157985.18","gene_symbol":"AGAP1","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:16922]","synonyms":"KIAA1099,GGAP1,CENTG2","biotype":"protein_coding","ncbi_id":"116987","summary":"This gene encodes a member of an ADP-ribosylation factor GTPase-activating protein family involved in membrane trafficking and cytoskeleton dynamics. This gene functions as a direct regulator of the adaptor-related protein complex 3 on endosomes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":235494089,"end":236131800,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:16922]"}, {"versioned_ensembl_gene_id":"ENSG00000260708.1","gene_symbol":"AL118516.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46761894,"end":46762563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211786.3","gene_symbol":"TRAV8-2","gene_name":"T-cell receptor alpha variable 8-2 [Source:HGNC Symbol;Acc:HGNC:12147]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28684","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21846537,"end":21847221,"strand":1,"description":"T-cell receptor alpha variable 8-2 [Source:HGNC Symbol;Acc:HGNC:12147]"}, {"versioned_ensembl_gene_id":"ENSG00000242296.2","gene_symbol":"DEFB109A","gene_name":"defensin beta 109A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18090]","synonyms":"DEFB109P1,DEFB109,DEFB-9","biotype":"unprocessed_pseudogene","ncbi_id":"245912","summary":null,"start":12393209,"end":12400366,"strand":-1,"description":"defensin beta 109A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18090]"}, {"versioned_ensembl_gene_id":"ENSG00000268743.1","gene_symbol":"AC008737.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16844025,"end":16846473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216359.1","gene_symbol":"AL139039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10514282,"end":10514973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264072.1","gene_symbol":"AP001180.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10627646,"end":10628846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266470.1","gene_symbol":"AP001180.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10632238,"end":10632396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263326.1","gene_symbol":"AC133552.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25071490,"end":25072727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273483.1","gene_symbol":"AL354760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112517799,"end":112518441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153558.13","gene_symbol":"FBXL2","gene_name":"F-box and leucine rich repeat protein 2 [Source:HGNC Symbol;Acc:HGNC:13598]","synonyms":"FBL3,FBL2","biotype":"protein_coding","ncbi_id":"25827","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains 12 tandem leucine-rich repeats. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":33277025,"end":33403662,"strand":1,"description":"F-box and leucine rich repeat protein 2 [Source:HGNC Symbol;Acc:HGNC:13598]"}, {"versioned_ensembl_gene_id":"ENSG00000228296.1","gene_symbol":"TTTY4C","gene_name":"testis-specific transcript, Y-linked 4C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31892]","synonyms":"LINC00125","biotype":"lincRNA","ncbi_id":"474150","summary":"There are three copies of this gene on chromosome Y. This record represents the most telomeric copy, which is within the P1 palindrome. [provided by RefSeq, Jul 2008]","start":25063083,"end":25099892,"strand":-1,"description":"testis-specific transcript, Y-linked 4C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31892]"}, {"versioned_ensembl_gene_id":"ENSG00000254423.1","gene_symbol":"AC087203.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12374366,"end":12375546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256075.1","gene_symbol":"AC008033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68473741,"end":68474902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250204.2","gene_symbol":"TTTY23B","gene_name":"testis-specific transcript, Y-linked 23B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37983]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100101121","summary":null,"start":6242446,"end":6245283,"strand":-1,"description":"testis-specific transcript, Y-linked 23B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37983]"}, {"versioned_ensembl_gene_id":"ENSG00000226227.1","gene_symbol":"BX120007.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32523454,"end":32523549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274124.1","gene_symbol":"AC074029.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48152817,"end":48153128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220204.1","gene_symbol":"AL035079.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34404663,"end":34404949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232705.2","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32466569,"end":32480224,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000157326.18","gene_symbol":"DHRS4","gene_name":"dehydrogenase/reductase 4 [Source:HGNC Symbol;Acc:HGNC:16985]","synonyms":"FLJ11008,SDR25C2,SDR-SRL,SCAD-SRL,humNRDR","biotype":"protein_coding","ncbi_id":"10901","summary":null,"start":23953586,"end":23969279,"strand":1,"description":"dehydrogenase/reductase 4 [Source:HGNC Symbol;Acc:HGNC:16985]"}, {"versioned_ensembl_gene_id":"ENSG00000205740.2","gene_symbol":"AL359878.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":971146,"end":988341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143162.7","gene_symbol":"CREG1","gene_name":"cellular repressor of E1A stimulated genes 1 [Source:HGNC Symbol;Acc:HGNC:2351]","synonyms":"CREG","biotype":"protein_coding","ncbi_id":"8804","summary":"The adenovirus E1A protein both activates and represses gene expression to promote cellular proliferation and inhibit differentiation. The protein encoded by this gene antagonizes transcriptional activation and cellular transformation by E1A. This protein shares limited sequence similarity with E1A and binds both the general transcription factor TBP and the tumor suppressor pRb in vitro. This gene may contribute to the transcriptional control of cell growth and differentiation. [provided by RefSeq, Jul 2008]","start":167529677,"end":167553767,"strand":-1,"description":"cellular repressor of E1A stimulated genes 1 [Source:HGNC Symbol;Acc:HGNC:2351]"}, {"versioned_ensembl_gene_id":"ENSG00000272017.1","gene_symbol":"AL137784.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99568097,"end":99569096,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270955.1","gene_symbol":"AC135731.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30282533,"end":30288389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264246.1","gene_symbol":"AP005208.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4430945,"end":4431152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253671.1","gene_symbol":"AC027117.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":17808941,"end":17820868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230475.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"D6S82E,BAT5,NG26","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31677699,"end":31694178,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000214077.4","gene_symbol":"GNAQP1","gene_name":"G protein subunit alpha q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4391]","synonyms":"GNAQP","biotype":"processed_pseudogene","ncbi_id":"2777","summary":null,"start":131423801,"end":131424867,"strand":-1,"description":"G protein subunit alpha q pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4391]"}, {"versioned_ensembl_gene_id":"ENSG00000239377.1","gene_symbol":"AC073111.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150379854,"end":150383885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240449.1","gene_symbol":"AC005586.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150363777,"end":150372590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251299.1","gene_symbol":"SLC25A15P3","gene_name":"solute carrier family 25 member 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39844]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422635","summary":null,"start":24943575,"end":24944498,"strand":1,"description":"solute carrier family 25 member 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39844]"}, {"versioned_ensembl_gene_id":"ENSG00000238140.1","gene_symbol":"AC104170.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51461721,"end":51463416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259403.1","gene_symbol":"AC020704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97272177,"end":97319288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239683.1","gene_symbol":"AC007998.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35383354,"end":35384025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189171.14","gene_symbol":"S100A13","gene_name":"S100 calcium binding protein A13 [Source:HGNC Symbol;Acc:HGNC:10490]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6284","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein is widely expressed in various types of tissues with a high expression level in thyroid gland. In smooth muscle cells, this protein co-expresses with other family members in the nucleus and in stress fibers, suggesting diverse functions in signal transduction. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":153618787,"end":153631360,"strand":-1,"description":"S100 calcium binding protein A13 [Source:HGNC Symbol;Acc:HGNC:10490]"}, {"versioned_ensembl_gene_id":"ENSG00000261455.1","gene_symbol":"LINC01003","gene_name":"long intergenic non-protein coding RNA 1003 [Source:HGNC Symbol;Acc:HGNC:48957]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128822","summary":null,"start":152463786,"end":152465549,"strand":1,"description":"long intergenic non-protein coding RNA 1003 [Source:HGNC Symbol;Acc:HGNC:48957]"}, {"versioned_ensembl_gene_id":"ENSG00000231341.1","gene_symbol":"VDAC1P6","gene_name":"voltage dependent anion channel 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37481]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359800","summary":null,"start":5207215,"end":5208069,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37481]"}, {"versioned_ensembl_gene_id":"ENSG00000217686.2","gene_symbol":"NUS1P4","gene_name":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130167","summary":null,"start":98610292,"end":98610876,"strand":-1,"description":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38474]"}, {"versioned_ensembl_gene_id":"ENSG00000104660.17","gene_symbol":"LEPROTL1","gene_name":"leptin receptor overlapping transcript like 1 [Source:HGNC Symbol;Acc:HGNC:6555]","synonyms":"Vps55,my047","biotype":"protein_coding","ncbi_id":"23484","summary":null,"start":30095398,"end":30177208,"strand":1,"description":"leptin receptor overlapping transcript like 1 [Source:HGNC Symbol;Acc:HGNC:6555]"}, {"versioned_ensembl_gene_id":"ENSG00000253708.1","gene_symbol":"AC026979.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30176554,"end":30180888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145649.7","gene_symbol":"GZMA","gene_name":"granzyme A [Source:HGNC Symbol;Acc:HGNC:4708]","synonyms":"HFSP,CTLA3","biotype":"protein_coding","ncbi_id":"3001","summary":"Cytolytic T lymphocytes (CTL) and natural killer (NK) cells share the remarkable ability to recognize, bind, and lyse specific target cells. They are thought to protect their host by lysing cells bearing on their surface 'nonself' antigens, usually peptides or proteins resulting from infection by intracellular pathogens. The protein described here is a T cell- and natural killer cell-specific serine protease that may function as a common component necessary for lysis of target cells by cytotoxic T lymphocytes and natural killer cells. [provided by RefSeq, Jul 2008]","start":55102648,"end":55110252,"strand":1,"description":"granzyme A [Source:HGNC Symbol;Acc:HGNC:4708]"}, {"versioned_ensembl_gene_id":"ENSG00000171560.14","gene_symbol":"FGA","gene_name":"fibrinogen alpha chain [Source:HGNC Symbol;Acc:HGNC:3661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2243","summary":"This gene encodes the alpha subunit of the coagulation factor fibrinogen, which is a component of the blood clot. Following vascular injury, the encoded preproprotein is proteolytically processed by thrombin during the conversion of fibrinogen to fibrin. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia and renal amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. [provided by RefSeq, Jan 2016]","start":154583126,"end":154590766,"strand":-1,"description":"fibrinogen alpha chain [Source:HGNC Symbol;Acc:HGNC:3661]"}, {"versioned_ensembl_gene_id":"ENSG00000260147.1","gene_symbol":"MTND5P34","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:51953]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075255","summary":null,"start":55007982,"end":55008306,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:51953]"}, {"versioned_ensembl_gene_id":"ENSG00000224507.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32397896,"end":32401073,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000237100.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30639263,"end":30645325,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000101935.9","gene_symbol":"AMMECR1","gene_name":"Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:HGNC:467]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9949","summary":"The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":110194186,"end":110440233,"strand":-1,"description":"Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:HGNC:467]"}, {"versioned_ensembl_gene_id":"ENSG00000185899.1","gene_symbol":"TAS2R60","gene_name":"taste 2 receptor member 60 [Source:HGNC Symbol;Acc:HGNC:20639]","synonyms":"T2R60","biotype":"protein_coding","ncbi_id":"338398","summary":"This gene encodes a member of the bitter taste receptor family which belong to the G protein-coupled receptor superfamily and are predominantly expressed in taste receptor cells of the tongue and palate epithelia. This intronless taste receptor gene encodes a seven-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered together with eight other taste receptor genes on chromosome 7. [provided by RefSeq, Jul 2017]","start":143443453,"end":143444409,"strand":1,"description":"taste 2 receptor member 60 [Source:HGNC Symbol;Acc:HGNC:20639]"}, {"versioned_ensembl_gene_id":"ENSG00000274681.2","gene_symbol":"SUDS3P1","gene_name":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285647","summary":null,"start":177974393,"end":177975358,"strand":1,"description":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]"}, {"versioned_ensembl_gene_id":"ENSG00000247324.2","gene_symbol":"AC010547.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71462278,"end":71465941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216649.3","gene_symbol":"GAGE12E","gene_name":"G antigen 12E [Source:HGNC Symbol;Acc:HGNC:31905]","synonyms":"OTTHUMG00000024146","biotype":"protein_coding","ncbi_id":"729431","summary":null,"start":49551333,"end":49558649,"strand":1,"description":"G antigen 12E [Source:HGNC Symbol;Acc:HGNC:31905]"}, {"versioned_ensembl_gene_id":"ENSG00000253142.1","gene_symbol":"AC037441.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22895434,"end":22897813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241790.2","gene_symbol":"ENO1P4","gene_name":"enolase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37945]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100885799","summary":null,"start":201621646,"end":201623430,"strand":-1,"description":"enolase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37945]"}, {"versioned_ensembl_gene_id":"ENSG00000111713.2","gene_symbol":"GYS2","gene_name":"glycogen synthase 2 [Source:HGNC Symbol;Acc:HGNC:4707]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2998","summary":"The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content. [provided by RefSeq, Dec 2009]","start":21536189,"end":21604847,"strand":-1,"description":"glycogen synthase 2 [Source:HGNC Symbol;Acc:HGNC:4707]"}, {"versioned_ensembl_gene_id":"ENSG00000223675.1","gene_symbol":"AC093117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94585556,"end":94592297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213600.3","gene_symbol":"U73169.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50239618,"end":50239984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270992.1","gene_symbol":"AC024085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130255902,"end":130262770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253706.5","gene_symbol":"AC011632.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74798784,"end":74866939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137090.11","gene_symbol":"DMRT1","gene_name":"doublesex and mab-3 related transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:2934]","synonyms":"DMT1,CT154","biotype":"protein_coding","ncbi_id":"1761","summary":"This gene is found in a cluster with two other members of the gene family, having in common a zinc finger-like DNA-binding motif (DM domain). The DM domain is an ancient, conserved component of the vertebrate sex-determining pathway that is also a key regulator of male development in flies and nematodes. This gene exhibits a gonad-specific and sexually dimorphic expression pattern. Defective testicular development and XY feminization occur when this gene is hemizygous. [provided by RefSeq, Jul 2008]","start":841690,"end":969090,"strand":1,"description":"doublesex and mab-3 related transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:2934]"}, {"versioned_ensembl_gene_id":"ENSG00000280232.1","gene_symbol":"AL589666.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85498441,"end":85499058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224472.6","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31237108,"end":31242737,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000116147.16","gene_symbol":"TNR","gene_name":"tenascin R [Source:HGNC Symbol;Acc:HGNC:11953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7143","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The encoded protein is restricted to the central nervous system. The protein may play a role in neurite outgrowth, neural cell adhesion and modulation of sodium channel function. It is a constituent of perineuronal nets. [provided by RefSeq, Aug 2013]","start":175315194,"end":175743770,"strand":-1,"description":"tenascin R [Source:HGNC Symbol;Acc:HGNC:11953]"}, {"versioned_ensembl_gene_id":"ENSG00000225878.1","gene_symbol":"SERBP1P2","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23967]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359996","summary":null,"start":4801685,"end":4802848,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23967]"}, {"versioned_ensembl_gene_id":"ENSG00000213081.3","gene_symbol":"AC012362.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208360631,"end":208361369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259542.5","gene_symbol":"AC087477.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96393146,"end":96405189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162999.12","gene_symbol":"DUSP19","gene_name":"dual specificity phosphatase 19 [Source:HGNC Symbol;Acc:HGNC:18894]","synonyms":"SKRP1,DUSP17","biotype":"protein_coding","ncbi_id":"142679","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP19 contains a variation of the consensus DUSP C-terminal catalytic domain, with the last serine residue replaced by alanine, and lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":183078559,"end":183100005,"strand":1,"description":"dual specificity phosphatase 19 [Source:HGNC Symbol;Acc:HGNC:18894]"}, {"versioned_ensembl_gene_id":"ENSG00000258373.1","gene_symbol":"SLC25A3P2","gene_name":"solute carrier family 25 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128618","summary":null,"start":111992996,"end":111993875,"strand":1,"description":"solute carrier family 25 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43784]"}, {"versioned_ensembl_gene_id":"ENSG00000230440.1","gene_symbol":"AL391119.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26132887,"end":26134198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170178.6","gene_symbol":"HOXD12","gene_name":"homeobox D12 [Source:HGNC Symbol;Acc:HGNC:5135]","synonyms":"HOX4H","biotype":"protein_coding","ncbi_id":"3238","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. The exact role of this gene has not been determined. [provided by RefSeq, Jul 2008]","start":176099730,"end":176101193,"strand":1,"description":"homeobox D12 [Source:HGNC Symbol;Acc:HGNC:5135]"}, {"versioned_ensembl_gene_id":"ENSG00000241370.5","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30345131,"end":30346884,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000196756.11","gene_symbol":"SNHG17","gene_name":"small nucleolar RNA host gene 17 [Source:HGNC Symbol;Acc:HGNC:48600]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"388796","summary":null,"start":38420588,"end":38435353,"strand":-1,"description":"small nucleolar RNA host gene 17 [Source:HGNC Symbol;Acc:HGNC:48600]"}, {"versioned_ensembl_gene_id":"ENSG00000101311.15","gene_symbol":"FERMT1","gene_name":"fermitin family member 1 [Source:HGNC Symbol;Acc:HGNC:15889]","synonyms":"KIND1,FLJ20116,C20orf42,URP1,UNC112A","biotype":"protein_coding","ncbi_id":"55612","summary":"This gene encodes a member of the fermitin family, and contains a FERM domain and a pleckstrin homology domain. The encoded protein is involved in integrin signaling and linkage of the actin cytoskeleton to the extracellular matrix. Mutations in this gene have been linked to Kindler syndrome. [provided by RefSeq, Dec 2009]","start":6074845,"end":6123544,"strand":-1,"description":"fermitin family member 1 [Source:HGNC Symbol;Acc:HGNC:15889]"}, {"versioned_ensembl_gene_id":"ENSG00000184221.12","gene_symbol":"OLIG1","gene_name":"oligodendrocyte transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:16983]","synonyms":"bHLHe21,BHLHB6","biotype":"protein_coding","ncbi_id":"116448","summary":null,"start":33070144,"end":33072420,"strand":1,"description":"oligodendrocyte transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:16983]"}, {"versioned_ensembl_gene_id":"ENSG00000048462.10","gene_symbol":"TNFRSF17","gene_name":"TNF receptor superfamily member 17 [Source:HGNC Symbol;Acc:HGNC:11913]","synonyms":"TNFRSF13A,CD269,BCMA,BCM","biotype":"protein_coding","ncbi_id":"608","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is preferentially expressed in mature B lymphocytes, and may be important for B cell development and autoimmune response. This receptor has been shown to specifically bind to the tumor necrosis factor (ligand) superfamily, member 13b (TNFSF13B/TALL-1/BAFF), and to lead to NF-kappaB and MAPK8/JNK activation. This receptor also binds to various TRAF family members, and thus may transduce signals for cell survival and proliferation. [provided by RefSeq, Jul 2008]","start":11965107,"end":11968068,"strand":1,"description":"TNF receptor superfamily member 17 [Source:HGNC Symbol;Acc:HGNC:11913]"}, {"versioned_ensembl_gene_id":"ENSG00000228961.1","gene_symbol":"LINC01690","gene_name":"long intergenic non-protein coding RNA 1690 [Source:HGNC Symbol;Acc:HGNC:52477]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32958888,"end":32960566,"strand":1,"description":"long intergenic non-protein coding RNA 1690 [Source:HGNC Symbol;Acc:HGNC:52477]"}, {"versioned_ensembl_gene_id":"ENSG00000236388.1","gene_symbol":"ITCH-AS1","gene_name":"ITCH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40659]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480737","summary":null,"start":34441592,"end":34442025,"strand":-1,"description":"ITCH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40659]"}, {"versioned_ensembl_gene_id":"ENSG00000183273.6","gene_symbol":"CCDC60","gene_name":"coiled-coil domain containing 60 [Source:HGNC Symbol;Acc:HGNC:28610]","synonyms":"MGC39827","biotype":"protein_coding","ncbi_id":"160777","summary":null,"start":119334712,"end":119541047,"strand":1,"description":"coiled-coil domain containing 60 [Source:HGNC Symbol;Acc:HGNC:28610]"}, {"versioned_ensembl_gene_id":"ENSG00000234933.1","gene_symbol":"CDC42P1","gene_name":"cell division cycle 42 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16339]","synonyms":"bK3216D2.3","biotype":"processed_pseudogene","ncbi_id":"170503","summary":null,"start":34402149,"end":34402696,"strand":-1,"description":"cell division cycle 42 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16339]"}, {"versioned_ensembl_gene_id":"ENSG00000232003.2","gene_symbol":"ZNF736P12Y","gene_name":"zinc finger protein 736 pseudogene 12, Y-linked [Source:HGNC Symbol;Acc:HGNC:38431]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419731","summary":null,"start":24500263,"end":24501505,"strand":-1,"description":"zinc finger protein 736 pseudogene 12, Y-linked [Source:HGNC Symbol;Acc:HGNC:38431]"}, {"versioned_ensembl_gene_id":"ENSG00000125434.10","gene_symbol":"SLC25A35","gene_name":"solute carrier family 25 member 35 [Source:HGNC Symbol;Acc:HGNC:31921]","synonyms":"FLJ40217","biotype":"protein_coding","ncbi_id":"399512","summary":"SLC25A35 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":8287763,"end":8295343,"strand":-1,"description":"solute carrier family 25 member 35 [Source:HGNC Symbol;Acc:HGNC:31921]"}, {"versioned_ensembl_gene_id":"ENSG00000219700.1","gene_symbol":"PTCHD3P3","gene_name":"patched domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44947]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533665","summary":null,"start":109288571,"end":109290503,"strand":-1,"description":"patched domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44947]"}, {"versioned_ensembl_gene_id":"ENSG00000272150.5","gene_symbol":"NBPF25P","gene_name":"NBPF member 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:45046]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101929780","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Sep 2013]","start":145572345,"end":145607858,"strand":-1,"description":"NBPF member 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:45046]"}, {"versioned_ensembl_gene_id":"ENSG00000162631.18","gene_symbol":"NTNG1","gene_name":"netrin G1 [Source:HGNC Symbol;Acc:HGNC:23319]","synonyms":"Lmnt1,KIAA0976","biotype":"protein_coding","ncbi_id":"22854","summary":"This gene encodes a preproprotein that is processed into a secreted protein containing eukaroytic growth factor (EGF)-like domains. This protein acts to guide axon growth during neuronal development. Polymorphisms in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2015]","start":107140007,"end":107483458,"strand":1,"description":"netrin G1 [Source:HGNC Symbol;Acc:HGNC:23319]"}, {"versioned_ensembl_gene_id":"ENSG00000262221.1","gene_symbol":"KRTAP9-7","gene_name":"keratin associated protein 9-7 [Source:HGNC Symbol;Acc:HGNC:18915]","synonyms":"KRTAP9L1,KAP9.7","biotype":"protein_coding","ncbi_id":"100505724","summary":null,"start":41264289,"end":41265327,"strand":1,"description":"keratin associated protein 9-7 [Source:HGNC Symbol;Acc:HGNC:18915]"}, {"versioned_ensembl_gene_id":"ENSG00000101152.10","gene_symbol":"DNAJC5","gene_name":"DnaJ heat shock protein family (Hsp40) member C5 [Source:HGNC Symbol;Acc:HGNC:16235]","synonyms":"FLJ00118,DNAJC5A,CLN4,FLJ13070","biotype":"protein_coding","ncbi_id":"80331","summary":"This gene is a member of the J protein family. J proteins function in many cellular processes by regulating the ATPase activity of 70 kDa heat shock proteins. The encoded protein plays a role in membrane trafficking and protein folding, and has been shown to have anti-neurodegenerative properties. The encoded protein is known to play a role in cystic fibrosis and Huntington's disease. A pseudogene of this gene is located on the short arm of chromosome 8. [provided by RefSeq, Nov 2010]","start":63895182,"end":63936031,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C5 [Source:HGNC Symbol;Acc:HGNC:16235]"}, {"versioned_ensembl_gene_id":"ENSG00000162490.6","gene_symbol":"DRAXIN","gene_name":"dorsal inhibitory axon guidance protein [Source:HGNC Symbol;Acc:HGNC:25054]","synonyms":"Neucrin,FLJ34999,Draxin,C1orf187","biotype":"protein_coding","ncbi_id":"374946","summary":null,"start":11691729,"end":11725857,"strand":1,"description":"dorsal inhibitory axon guidance protein [Source:HGNC Symbol;Acc:HGNC:25054]"}, {"versioned_ensembl_gene_id":"ENSG00000280935.1","gene_symbol":"FABP5P13","gene_name":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]","synonyms":"FABP5L13","biotype":"processed_pseudogene","ncbi_id":"106480712","summary":null,"start":526465,"end":526792,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38717]"}, {"versioned_ensembl_gene_id":"ENSG00000267766.1","gene_symbol":"AC022726.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":63151114,"end":63151320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270098.1","gene_symbol":"AC079230.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71434405,"end":71437924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281542.1","gene_symbol":"AL021878.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42089630,"end":42090028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281364.1","gene_symbol":"AC217769.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45551530,"end":45556925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127324.8","gene_symbol":"TSPAN8","gene_name":"tetraspanin 8 [Source:HGNC Symbol;Acc:HGNC:11855]","synonyms":"TM4SF3,CO-029","biotype":"protein_coding","ncbi_id":"7103","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins. This gene is expressed in different carcinomas. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":71125085,"end":71441898,"strand":-1,"description":"tetraspanin 8 [Source:HGNC Symbol;Acc:HGNC:11855]"}, {"versioned_ensembl_gene_id":"ENSG00000238257.1","gene_symbol":"AP000244.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30762682,"end":30762882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253774.1","gene_symbol":"AC114550.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8559894,"end":8562124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163840.9","gene_symbol":"DTX3L","gene_name":"deltex E3 ubiquitin ligase 3L [Source:HGNC Symbol;Acc:HGNC:30323]","synonyms":"BBAP","biotype":"protein_coding","ncbi_id":"151636","summary":"DTX3L functions as an E3 ubiquitin ligase (Takeyama et al., 2003 [PubMed 12670957]).[supplied by OMIM, Nov 2009]","start":122564238,"end":122575203,"strand":1,"description":"deltex E3 ubiquitin ligase 3L [Source:HGNC Symbol;Acc:HGNC:30323]"}, {"versioned_ensembl_gene_id":"ENSG00000187005.4","gene_symbol":"KRTAP21-1","gene_name":"keratin associated protein 21-1 [Source:HGNC Symbol;Acc:HGNC:18945]","synonyms":"KAP21.1","biotype":"protein_coding","ncbi_id":"337977","summary":null,"start":30754830,"end":30755428,"strand":-1,"description":"keratin associated protein 21-1 [Source:HGNC Symbol;Acc:HGNC:18945]"}, {"versioned_ensembl_gene_id":"ENSG00000153006.15","gene_symbol":"SREK1IP1","gene_name":"SREK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26716]","synonyms":"SFRS12IP1,P18SRP,FLJ36754","biotype":"protein_coding","ncbi_id":"285672","summary":null,"start":64718144,"end":64768685,"strand":-1,"description":"SREK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26716]"}, {"versioned_ensembl_gene_id":"ENSG00000151353.14","gene_symbol":"TMEM18","gene_name":"transmembrane protein 18 [Source:HGNC Symbol;Acc:HGNC:25257]","synonyms":"lncND,DKFZp434C1714","biotype":"protein_coding","ncbi_id":"129787","summary":null,"start":667335,"end":677439,"strand":-1,"description":"transmembrane protein 18 [Source:HGNC Symbol;Acc:HGNC:25257]"}, {"versioned_ensembl_gene_id":"ENSG00000232882.1","gene_symbol":"PHKA1P1","gene_name":"phosphorylase kinase regulatory subunit alpha 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:33919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646780","summary":null,"start":90892992,"end":90893612,"strand":-1,"description":"phosphorylase kinase regulatory subunit alpha 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:33919]"}, {"versioned_ensembl_gene_id":"ENSG00000243279.3","gene_symbol":"PRAF2","gene_name":"PRA1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:28911]","synonyms":"Yip6a,JM4","biotype":"protein_coding","ncbi_id":"11230","summary":null,"start":49071156,"end":49074071,"strand":-1,"description":"PRA1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:28911]"}, {"versioned_ensembl_gene_id":"ENSG00000224427.1","gene_symbol":"AP000281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32841496,"end":32841811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212938.3","gene_symbol":"KRTAP6-3","gene_name":"keratin associated protein 6-3 [Source:HGNC Symbol;Acc:HGNC:18933]","synonyms":"KAP6.3","biotype":"protein_coding","ncbi_id":"337968","summary":null,"start":30592440,"end":30593075,"strand":1,"description":"keratin associated protein 6-3 [Source:HGNC Symbol;Acc:HGNC:18933]"}, {"versioned_ensembl_gene_id":"ENSG00000240571.1","gene_symbol":"AC087071.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130173718,"end":130205361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243635.1","gene_symbol":"AC091804.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104502700,"end":104503266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227736.1","gene_symbol":"MTCO3P16","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52046]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075155","summary":null,"start":201552859,"end":201553612,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52046]"}, {"versioned_ensembl_gene_id":"ENSG00000227028.6","gene_symbol":"SLC8A1-AS1","gene_name":"SLC8A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44102]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128590","summary":null,"start":39786453,"end":40255209,"strand":1,"description":"SLC8A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44102]"}, {"versioned_ensembl_gene_id":"ENSG00000163081.2","gene_symbol":"CCDC140","gene_name":"coiled-coil domain containing 140 [Source:HGNC Symbol;Acc:HGNC:26514]","synonyms":"FLJ32447","biotype":"protein_coding","ncbi_id":"151278","summary":"This gene encodes a protein that appears to be restricted to select higher primate species. This protein contains a C-terminal coiled-coil domain, which is a versatile structural motif consisting of multiple amphipathic alpha-helices that twist around each other to form a supercoil. [provided by RefSeq, Aug 2011]","start":222298147,"end":222305217,"strand":1,"description":"coiled-coil domain containing 140 [Source:HGNC Symbol;Acc:HGNC:26514]"}, {"versioned_ensembl_gene_id":"ENSG00000257224.1","gene_symbol":"CR383656.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18702281,"end":18702463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175274.18","gene_symbol":"TP53I11","gene_name":"tumor protein p53 inducible protein 11 [Source:HGNC Symbol;Acc:HGNC:16842]","synonyms":"PIG11","biotype":"protein_coding","ncbi_id":"9537","summary":null,"start":44885903,"end":44951306,"strand":-1,"description":"tumor protein p53 inducible protein 11 [Source:HGNC Symbol;Acc:HGNC:16842]"}, {"versioned_ensembl_gene_id":"ENSG00000281942.1","gene_symbol":"AC068473.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":79576460,"end":79589010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187961.13","gene_symbol":"KLHL17","gene_name":"kelch like family member 17 [Source:HGNC Symbol;Acc:HGNC:24023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339451","summary":"The protein encoded by this gene is expressed in neurons of most regions of the brain. It contains an N-terminal BTB domain, which mediates dimerization of the protein, and a C-terminal Kelch domain, which mediates binding to F-actin. This protein may play a key role in the regulation of actin-based neuronal function. [provided by RefSeq, Aug 2010]","start":960587,"end":965715,"strand":1,"description":"kelch like family member 17 [Source:HGNC Symbol;Acc:HGNC:24023]"}, {"versioned_ensembl_gene_id":"ENSG00000268203.1","gene_symbol":"AC010503.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6494320,"end":6494805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177133.10","gene_symbol":"LINC00982","gene_name":"long intergenic non-protein coding RNA 982 [Source:HGNC Symbol;Acc:HGNC:48664]","synonyms":"FLJ42875","biotype":"antisense_RNA","ncbi_id":"440556","summary":null,"start":3059615,"end":3068437,"strand":-1,"description":"long intergenic non-protein coding RNA 982 [Source:HGNC Symbol;Acc:HGNC:48664]"}, {"versioned_ensembl_gene_id":"ENSG00000253372.5","gene_symbol":"AC016405.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":122807746,"end":122816517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164708.5","gene_symbol":"PGAM2","gene_name":"phosphoglycerate mutase 2 [Source:HGNC Symbol;Acc:HGNC:8889]","synonyms":"PGAM-M","biotype":"protein_coding","ncbi_id":"5224","summary":"Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. [provided by RefSeq, Sep 2009]","start":44062727,"end":44065587,"strand":-1,"description":"phosphoglycerate mutase 2 [Source:HGNC Symbol;Acc:HGNC:8889]"}, {"versioned_ensembl_gene_id":"ENSG00000271530.1","gene_symbol":"WBP1LP12","gene_name":"WW domain binding protein 1-like pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51472]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480327","summary":null,"start":95124,"end":95454,"strand":1,"description":"WW domain binding protein 1-like pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51472]"}, {"versioned_ensembl_gene_id":"ENSG00000280741.1","gene_symbol":"LINC00685","gene_name":"long intergenic non-protein coding RNA 685 [Source:HGNC Symbol;Acc:HGNC:27560]","synonyms":"PPP2R3B-AS1,OTTHUMT00000055574,NCRNA00107,CXYorf10","biotype":"antisense_RNA","ncbi_id":"283981","summary":null,"start":320990,"end":321711,"strand":1,"description":"long intergenic non-protein coding RNA 685 [Source:HGNC Symbol;Acc:HGNC:27560]"}, {"versioned_ensembl_gene_id":"ENSG00000281317.1","gene_symbol":"BTG3-AS1","gene_name":"BTG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53145]","synonyms":"ASBEL","biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":17611744,"end":17633199,"strand":1,"description":"BTG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53145]"}, {"versioned_ensembl_gene_id":"ENSG00000236691.3","gene_symbol":"NDUFA4P2","gene_name":"NDUFA4, mitochondrial complex associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31362]","synonyms":"NDUFA4L,bcm1723","biotype":"processed_pseudogene","ncbi_id":"100287880","summary":null,"start":103240987,"end":103241230,"strand":1,"description":"NDUFA4, mitochondrial complex associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31362]"}, {"versioned_ensembl_gene_id":"ENSG00000235200.2","gene_symbol":"LINC01702","gene_name":"long intergenic non-protein coding RNA 1702 [Source:HGNC Symbol;Acc:HGNC:52490]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724481","summary":null,"start":67522347,"end":67532612,"strand":1,"description":"long intergenic non-protein coding RNA 1702 [Source:HGNC Symbol;Acc:HGNC:52490]"}, {"versioned_ensembl_gene_id":"ENSG00000257058.1","gene_symbol":"AP001363.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62545999,"end":62547699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266835.5","gene_symbol":"GAPLINC","gene_name":"gastric adenocarcinoma associated, positive CD44 regulator, long intergenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51308]","synonyms":"TCONS_00026238,LINC01540","biotype":"lincRNA","ncbi_id":"100505592","summary":null,"start":3466250,"end":3478978,"strand":1,"description":"gastric adenocarcinoma associated, positive CD44 regulator, long intergenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:51308]"}, {"versioned_ensembl_gene_id":"ENSG00000254317.1","gene_symbol":"AC022973.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129832301,"end":129844504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234155.1","gene_symbol":"LINC02535","gene_name":"long intergenic non-protein coding RNA 2535 [Source:HGNC Symbol;Acc:HGNC:53569]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928820","summary":null,"start":85387219,"end":85390186,"strand":-1,"description":"long intergenic non-protein coding RNA 2535 [Source:HGNC Symbol;Acc:HGNC:53569]"}, {"versioned_ensembl_gene_id":"ENSG00000249956.4","gene_symbol":"UGT2B24P","gene_name":"UDP glucuronosyltransferase family 2 member B24, pseudogene [Source:HGNC Symbol;Acc:HGNC:12548]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54572","summary":null,"start":69408828,"end":69423164,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B24, pseudogene [Source:HGNC Symbol;Acc:HGNC:12548]"}, {"versioned_ensembl_gene_id":"ENSG00000165997.4","gene_symbol":"ARL5B","gene_name":"ADP ribosylation factor like GTPase 5B [Source:HGNC Symbol;Acc:HGNC:23052]","synonyms":"ARL8","biotype":"protein_coding","ncbi_id":"221079","summary":"ARL5B (ARL8) belongs to a family of proteins that are structurally similar to ADP-ribosylation factors (ARFs; see MIM 103180). ARLs and ARFs are part of the RAS superfamily of regulatory GTPases.[supplied by OMIM, Nov 2010]","start":18659405,"end":18681639,"strand":1,"description":"ADP ribosylation factor like GTPase 5B [Source:HGNC Symbol;Acc:HGNC:23052]"}, {"versioned_ensembl_gene_id":"ENSG00000215067.9","gene_symbol":"ALOX12-AS1","gene_name":"ALOX12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51342]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506713","summary":null,"start":6876635,"end":7012349,"strand":-1,"description":"ALOX12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51342]"}, {"versioned_ensembl_gene_id":"ENSG00000230839.1","gene_symbol":"AL121760.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1804016,"end":1817606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242110.7","gene_symbol":"AMACR","gene_name":"alpha-methylacyl-CoA racemase [Source:HGNC Symbol;Acc:HGNC:451]","synonyms":"RACE,P504S","biotype":"protein_coding","ncbi_id":"23600","summary":"This gene encodes a racemase. The encoded enzyme interconverts pristanoyl-CoA and C27-bile acylCoAs between their (R)- and (S)-stereoisomers. The conversion to the (S)-stereoisomers is necessary for degradation of these substrates by peroxisomal beta-oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult-onset sensorimotor neuropathy, pigmentary retinopathy, and adrenomyeloneuropathy due to defects in bile acid synthesis. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the upstream neighboring C1QTNF3 (C1q and tumor necrosis factor related protein 3) gene. [provided by RefSeq, Mar 2011]","start":33986178,"end":34008108,"strand":-1,"description":"alpha-methylacyl-CoA racemase [Source:HGNC Symbol;Acc:HGNC:451]"}, {"versioned_ensembl_gene_id":"ENSG00000271219.1","gene_symbol":"AC011626.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121113358,"end":121113919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239801.1","gene_symbol":"DENND6A-AS1","gene_name":"DENND6A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41152]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106144528","summary":null,"start":57628810,"end":57654918,"strand":1,"description":"DENND6A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41152]"}, {"versioned_ensembl_gene_id":"ENSG00000182631.6","gene_symbol":"RXFP3","gene_name":"relaxin/insulin like family peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:24883]","synonyms":"SALPR,RXFPR3,RLN3R1,GPCR135","biotype":"protein_coding","ncbi_id":"51289","summary":null,"start":33936386,"end":33938237,"strand":1,"description":"relaxin/insulin like family peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:24883]"}, {"versioned_ensembl_gene_id":"ENSG00000144320.13","gene_symbol":"LNPK","gene_name":"lunapark, ER junction formation factor [Source:HGNC Symbol;Acc:HGNC:21610]","synonyms":"Ul,LNP1,LNP,KIAA1715","biotype":"protein_coding","ncbi_id":"80856","summary":null,"start":175923892,"end":176002839,"strand":-1,"description":"lunapark, ER junction formation factor [Source:HGNC Symbol;Acc:HGNC:21610]"}, {"versioned_ensembl_gene_id":"ENSG00000267415.1","gene_symbol":"AC011471.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":6176256,"end":6176442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152520.13","gene_symbol":"PAN3","gene_name":"PAN3 poly(A) specific ribonuclease subunit [Source:HGNC Symbol;Acc:HGNC:29991]","synonyms":null,"biotype":"protein_coding","ncbi_id":"255967","summary":null,"start":28138506,"end":28295335,"strand":1,"description":"PAN3 poly(A) specific ribonuclease subunit [Source:HGNC Symbol;Acc:HGNC:29991]"}, {"versioned_ensembl_gene_id":"ENSG00000271173.1","gene_symbol":"AL355989.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43728217,"end":43728728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176532.3","gene_symbol":"PRR15","gene_name":"proline rich 15 [Source:HGNC Symbol;Acc:HGNC:22310]","synonyms":null,"biotype":"protein_coding","ncbi_id":"222171","summary":null,"start":29563811,"end":29567295,"strand":1,"description":"proline rich 15 [Source:HGNC Symbol;Acc:HGNC:22310]"}, {"versioned_ensembl_gene_id":"ENSG00000235017.9","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31885329,"end":31933220,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000173567.14","gene_symbol":"ADGRF3","gene_name":"adhesion G protein-coupled receptor F3 [Source:HGNC Symbol;Acc:HGNC:18989]","synonyms":"PGR23,hGPCR37,GPR113","biotype":"protein_coding","ncbi_id":"165082","summary":null,"start":26308173,"end":26346817,"strand":-1,"description":"adhesion G protein-coupled receptor F3 [Source:HGNC Symbol;Acc:HGNC:18989]"}, {"versioned_ensembl_gene_id":"ENSG00000270017.1","gene_symbol":"AC107976.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94855586,"end":94857011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122025.14","gene_symbol":"FLT3","gene_name":"fms related tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:3765]","synonyms":"STK1,FLK2,CD135","biotype":"protein_coding","ncbi_id":"2322","summary":"This gene encodes a class III receptor tyrosine kinase that regulates hematopoiesis. This receptor is activated by binding of the fms-related tyrosine kinase 3 ligand to the extracellular domain, which induces homodimer formation in the plasma membrane leading to autophosphorylation of the receptor. The activated receptor kinase subsequently phosphorylates and activates multiple cytoplasmic effector molecules in pathways involved in apoptosis, proliferation, and differentiation of hematopoietic cells in bone marrow. Mutations that result in the constitutive activation of this receptor result in acute myeloid leukemia and acute lymphoblastic leukemia. [provided by RefSeq, Jan 2015]","start":28003274,"end":28100592,"strand":-1,"description":"fms related tyrosine kinase 3 [Source:HGNC Symbol;Acc:HGNC:3765]"}, {"versioned_ensembl_gene_id":"ENSG00000188092.14","gene_symbol":"GPR89B","gene_name":"G protein-coupled receptor 89B [Source:HGNC Symbol;Acc:HGNC:13840]","synonyms":"SH120,GPR89C,GPR89","biotype":"protein_coding","ncbi_id":"51463","summary":null,"start":147928393,"end":147993521,"strand":1,"description":"G protein-coupled receptor 89B [Source:HGNC Symbol;Acc:HGNC:13840]"}, {"versioned_ensembl_gene_id":"ENSG00000254013.1","gene_symbol":"AC044849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30027713,"end":30028900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225465.8","gene_symbol":"RFPL1S","gene_name":"RFPL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:9978]","synonyms":"RFPL1-AS1,RFPL1-AS,NCRNA00006","biotype":"antisense_RNA","ncbi_id":"10740","summary":null,"start":29436534,"end":29478175,"strand":-1,"description":"RFPL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:9978]"}, {"versioned_ensembl_gene_id":"ENSG00000172046.18","gene_symbol":"USP19","gene_name":"ubiquitin specific peptidase 19 [Source:HGNC Symbol;Acc:HGNC:12617]","synonyms":"ZMYND9,KIAA0891","biotype":"protein_coding","ncbi_id":"10869","summary":"Protein ubiquitination controls many intracellular processes, including cell cycle progression, transcriptional activation, and signal transduction. This dynamic process, involving ubiquitin conjugating enzymes and deubiquitinating enzymes, adds and removes ubiquitin. Deubiquitinating enzymes are cysteine proteases that specifically cleave ubiquitin from ubiquitin-conjugated protein substrates. This protein is a ubiquitin protein ligase and plays a role in muscle wasting. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2017]","start":49108046,"end":49120938,"strand":-1,"description":"ubiquitin specific peptidase 19 [Source:HGNC Symbol;Acc:HGNC:12617]"}, {"versioned_ensembl_gene_id":"ENSG00000248318.1","gene_symbol":"AC104958.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120761253,"end":120776832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128159.11","gene_symbol":"TUBGCP6","gene_name":"tubulin gamma complex associated protein 6 [Source:HGNC Symbol;Acc:HGNC:18127]","synonyms":"KIAA1669,GCP6,DJ402G11.6","biotype":"protein_coding","ncbi_id":"85378","summary":"The protein encoded by this gene is part of a large multisubunit complex required for microtubule nucleation at the centrosome. [provided by RefSeq, Jul 2008]","start":50217689,"end":50244992,"strand":-1,"description":"tubulin gamma complex associated protein 6 [Source:HGNC Symbol;Acc:HGNC:18127]"}, {"versioned_ensembl_gene_id":"ENSG00000166069.13","gene_symbol":"TMCO5A","gene_name":"transmembrane and coiled-coil domains 5A [Source:HGNC Symbol;Acc:HGNC:28558]","synonyms":"TMCO5,MGC35118","biotype":"protein_coding","ncbi_id":"145942","summary":null,"start":37921939,"end":37967724,"strand":1,"description":"transmembrane and coiled-coil domains 5A [Source:HGNC Symbol;Acc:HGNC:28558]"}, {"versioned_ensembl_gene_id":"ENSG00000270012.1","gene_symbol":"AC232271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49273054,"end":49275768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232986.1","gene_symbol":"AL139081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33657436,"end":33659928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230490.2","gene_symbol":"AL139383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33355206,"end":33676768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237458.1","gene_symbol":"TUBB4BP3","gene_name":"tubulin beta 4B class IVb pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480746","summary":null,"start":118128748,"end":118129018,"strand":1,"description":"tubulin beta 4B class IVb pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42331]"}, {"versioned_ensembl_gene_id":"ENSG00000239392.2","gene_symbol":"AL354989.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34133157,"end":34134696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142694.6","gene_symbol":"EVA1B","gene_name":"eva-1 homolog B [Source:HGNC Symbol;Acc:HGNC:25558]","synonyms":"FLJ10647,FAM176B,C1orf78","biotype":"protein_coding","ncbi_id":"55194","summary":null,"start":36322031,"end":36324154,"strand":-1,"description":"eva-1 homolog B [Source:HGNC Symbol;Acc:HGNC:25558]"}, {"versioned_ensembl_gene_id":"ENSG00000049769.12","gene_symbol":"PPP1R3F","gene_name":"protein phosphatase 1 regulatory subunit 3F [Source:HGNC Symbol;Acc:HGNC:14944]","synonyms":"Hb2E","biotype":"protein_coding","ncbi_id":"89801","summary":"This gene encodes a protein that has been identified as one of several type-1 protein phosphatase (PP1) regulatory subunits. One or two of these subunits, together with the well-conserved catalytic subunit, can form the PP1 holoenzyme, where the regulatory subunit functions to regulate substrate specificity and/or targeting to a particular cellular compartment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":49269843,"end":49301461,"strand":1,"description":"protein phosphatase 1 regulatory subunit 3F [Source:HGNC Symbol;Acc:HGNC:14944]"}, {"versioned_ensembl_gene_id":"ENSG00000231682.1","gene_symbol":"LINC01891","gene_name":"long intergenic non-protein coding RNA 1891 [Source:HGNC Symbol;Acc:HGNC:52710]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373934","summary":null,"start":234444590,"end":234454595,"strand":-1,"description":"long intergenic non-protein coding RNA 1891 [Source:HGNC Symbol;Acc:HGNC:52710]"}, {"versioned_ensembl_gene_id":"ENSG00000260389.1","gene_symbol":"WBP11P1","gene_name":"WW domain binding protein 11 pseudogene 1 [Source:NCBI gene;Acc:441818]","synonyms":"HsT3017","biotype":"transcribed_processed_pseudogene","ncbi_id":"441818","summary":null,"start":32511663,"end":32514634,"strand":1,"description":"WW domain binding protein 11 pseudogene 1 [Source:NCBI gene;Acc:441818]"}, {"versioned_ensembl_gene_id":"ENSG00000232839.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30316726,"end":30333982,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000272931.1","gene_symbol":"AC099568.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89820174,"end":89820868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282994.1","gene_symbol":"AC215524.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190195738,"end":190195978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261914.2","gene_symbol":"RPL23AP84","gene_name":"ribosomal protein L23a pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:51575]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723981","summary":null,"start":190195727,"end":190196190,"strand":1,"description":"ribosomal protein L23a pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:51575]"}, {"versioned_ensembl_gene_id":"ENSG00000044459.14","gene_symbol":"CNTLN","gene_name":"centlein [Source:HGNC Symbol;Acc:HGNC:23432]","synonyms":"OTTHUMG00000019597,FLJ20276,C9orf39,C9orf101,bA340N12.1","biotype":"protein_coding","ncbi_id":"54875","summary":null,"start":17134982,"end":17503923,"strand":1,"description":"centlein [Source:HGNC Symbol;Acc:HGNC:23432]"}, {"versioned_ensembl_gene_id":"ENSG00000178295.14","gene_symbol":"GEN1","gene_name":"GEN1, Holliday junction 5' flap endonuclease [Source:HGNC Symbol;Acc:HGNC:26881]","synonyms":"Gen,FLJ40869","biotype":"protein_coding","ncbi_id":"348654","summary":"This gene encodes a member of the Rad2/xeroderma pigmentosum group G nuclease family, whose members are characterized by N-terminal and internal xeroderma pigmentosum group G nuclease domains followed by helix-hairpin-helix domains and disordered C-terminal domains. The protein encoded by this gene is involved in resolution of Holliday junctions, which are intermediate four-way structures that covalently link DNA during homologous recombination and double-strand break repair. The protein resolves Holliday junctions by creating dual incisions across the junction to produce nicked duplex products that can be ligated. In addition, this protein has been found to localize to centrosomes where it has been implicated in regulation of centrosome integrity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":17753858,"end":17788941,"strand":1,"description":"GEN1, Holliday junction 5' flap endonuclease [Source:HGNC Symbol;Acc:HGNC:26881]"}, {"versioned_ensembl_gene_id":"ENSG00000268804.1","gene_symbol":"LINC02132","gene_name":"long intergenic non-protein coding RNA 2132 [Source:HGNC Symbol;Acc:HGNC:52992]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984811","summary":null,"start":85935281,"end":85936223,"strand":-1,"description":"long intergenic non-protein coding RNA 2132 [Source:HGNC Symbol;Acc:HGNC:52992]"}, {"versioned_ensembl_gene_id":"ENSG00000224854.3","gene_symbol":"CDKN2A-AS1","gene_name":"CDKN2A antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:23831]","synonyms":"C9orf53,bA149I2.3","biotype":"lincRNA","ncbi_id":"51198","summary":null,"start":21966929,"end":21967751,"strand":1,"description":"CDKN2A antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:23831]"}, {"versioned_ensembl_gene_id":"ENSG00000248185.1","gene_symbol":"AC025445.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63301523,"end":63302056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244128.5","gene_symbol":"LINC01322","gene_name":"long intergenic non-protein coding RNA 1322 [Source:HGNC Symbol;Acc:HGNC:50528]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103695433","summary":null,"start":165206960,"end":165655423,"strand":1,"description":"long intergenic non-protein coding RNA 1322 [Source:HGNC Symbol;Acc:HGNC:50528]"}, {"versioned_ensembl_gene_id":"ENSG00000069206.15","gene_symbol":"ADAM7","gene_name":"ADAM metallopeptidase domain 7 [Source:HGNC Symbol;Acc:HGNC:214]","synonyms":"GP-83,EAPI","biotype":"protein_coding","ncbi_id":"8756","summary":"This gene encodes a member of the ADAMs family of zinc proteases. These transmembrane proteins play roles in multiple processes including cell signaling, adhesion and migration. The encoded protein lacks protease activity and may play roles in protein-protein interactions and cell adhesion processes including sperm-egg fusion. Mutations in this gene may be involved in the progression of melanoma. [provided by RefSeq, Oct 2011]","start":24440930,"end":24526970,"strand":1,"description":"ADAM metallopeptidase domain 7 [Source:HGNC Symbol;Acc:HGNC:214]"}, {"versioned_ensembl_gene_id":"ENSG00000234052.1","gene_symbol":"LINC01673","gene_name":"long intergenic non-protein coding RNA 1673 [Source:HGNC Symbol;Acc:HGNC:52461]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372763","summary":null,"start":27638693,"end":27653491,"strand":1,"description":"long intergenic non-protein coding RNA 1673 [Source:HGNC Symbol;Acc:HGNC:52461]"}, {"versioned_ensembl_gene_id":"ENSG00000262117.5","gene_symbol":"BCAR4","gene_name":"breast cancer anti-estrogen resistance 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22170]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400500","summary":"This gene produces a spliced long non-coding RNA (lncRNA) that has been implicated in breast cancer metastasis. It was originally identified in a screen for genes responsible for the development of resistance to anti-estrogens in breast cancer cells. It is thought that release of CCL21 enables this lncRNA to bind to the SNIP1 and PNUTS transcription factors, thereby activating a non-canonical GLI-dependent hedgehog signaling pathway that promotes cancer cell migration and invasion. A similar gene in cow expresses a protein in mature oocytes and preimplantation embryos. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2015]","start":11819829,"end":11828845,"strand":-1,"description":"breast cancer anti-estrogen resistance 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22170]"}, {"versioned_ensembl_gene_id":"ENSG00000214259.3","gene_symbol":"AC018695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85815873,"end":85816536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228192.7","gene_symbol":"AL512353.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42834681,"end":42846422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121634.5","gene_symbol":"GJA8","gene_name":"gap junction protein alpha 8 [Source:HGNC Symbol;Acc:HGNC:4281]","synonyms":"CZP1,CX50,CAE1,CAE","biotype":"protein_coding","ncbi_id":"2703","summary":"This gene encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. The encoded protein is a component of gap junction channels and functions in a calcium and pH-dependent manner. Mutations in this gene have been associated with zonular pulverulent cataracts, nuclear progressive cataracts, and cataract-microcornea syndrome. [provided by RefSeq, Dec 2009]","start":147907956,"end":147909257,"strand":1,"description":"gap junction protein alpha 8 [Source:HGNC Symbol;Acc:HGNC:4281]"}, {"versioned_ensembl_gene_id":"ENSG00000177595.17","gene_symbol":"PIDD1","gene_name":"p53-induced death domain protein 1 [Source:HGNC Symbol;Acc:HGNC:16491]","synonyms":"PIDD,MGC16925,LRDD,DKFZp434D229","biotype":"protein_coding","ncbi_id":"55367","summary":"The protein encoded by this gene contains a leucine-rich repeat and a death domain. This protein has been shown to interact with other death domain proteins, such as Fas (TNFRSF6)-associated via death domain (FADD) and MAP-kinase activating death domain-containing protein (MADD), and thus may function as an adaptor protein in cell death-related signaling processes. The expression of the mouse counterpart of this gene has been found to be positively regulated by the tumor suppressor p53 and to induce cell apoptosis in response to DNA damage, which suggests a role for this gene as an effector of p53-dependent apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":799179,"end":809753,"strand":-1,"description":"p53-induced death domain protein 1 [Source:HGNC Symbol;Acc:HGNC:16491]"}, {"versioned_ensembl_gene_id":"ENSG00000273253.2","gene_symbol":"AL022328.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50199090,"end":50200837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278461.4","gene_symbol":"MRPS36","gene_name":"mitochondrial ribosomal protein S36 [Source:HGNC Symbol;Acc:HGNC:16631]","synonyms":"MRP-S36,DC47","biotype":"protein_coding","ncbi_id":"92259","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. The mitochondrial ribosome (mitoribosome) consists of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. Pseudogenes corresponding to this gene are found on chromosomes 3p, 4q, 8p, 11q, 12q, and 20p. [provided by RefSeq, Jul 2008]","start":69217760,"end":69230127,"strand":1,"description":"mitochondrial ribosomal protein S36 [Source:HGNC Symbol;Acc:HGNC:16631]"}, {"versioned_ensembl_gene_id":"ENSG00000180999.10","gene_symbol":"C1orf105","gene_name":"chromosome 1 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:29591]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92346","summary":null,"start":172420688,"end":172468831,"strand":1,"description":"chromosome 1 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:29591]"}, {"versioned_ensembl_gene_id":"ENSG00000230928.1","gene_symbol":"AL139241.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98252023,"end":98256575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163156.11","gene_symbol":"SCNM1","gene_name":"sodium channel modifier 1 [Source:HGNC Symbol;Acc:HGNC:23136]","synonyms":"MGC3180","biotype":"protein_coding","ncbi_id":"79005","summary":"SCNM1 is a zinc finger protein and putative splicing factor. In mice, Scnm1 modifies phenotypic expression of Scn8a (MIM 600702) mutations (Buchner et al., 2003 [PubMed 12920299]).[supplied by OMIM, Oct 2009]","start":151156664,"end":151170297,"strand":1,"description":"sodium channel modifier 1 [Source:HGNC Symbol;Acc:HGNC:23136]"}, {"versioned_ensembl_gene_id":"ENSG00000143110.11","gene_symbol":"C1orf162","gene_name":"chromosome 1 open reading frame 162 [Source:HGNC Symbol;Acc:HGNC:28344]","synonyms":"MGC24133","biotype":"protein_coding","ncbi_id":"128346","summary":null,"start":111473792,"end":111478512,"strand":1,"description":"chromosome 1 open reading frame 162 [Source:HGNC Symbol;Acc:HGNC:28344]"}, {"versioned_ensembl_gene_id":"ENSG00000235779.7","gene_symbol":"AC079779.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":305111,"end":314367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167232.13","gene_symbol":"ZNF91","gene_name":"zinc finger protein 91 [Source:HGNC Symbol;Acc:HGNC:13166]","synonyms":"HTF10,HPF7","biotype":"protein_coding","ncbi_id":"7644","summary":"The ZNF91 gene encodes a zinc finger protein of the KRAB (Kruppel-associated box) subfamily (Bellefroid et al., 1991, 1993 [PubMed 2023909] [PubMed 8467795]).[supplied by OMIM, May 2010]","start":23304991,"end":23395560,"strand":-1,"description":"zinc finger protein 91 [Source:HGNC Symbol;Acc:HGNC:13166]"}, {"versioned_ensembl_gene_id":"ENSG00000282372.1","gene_symbol":"PABPC1P8","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37988]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132766","summary":null,"start":42265530,"end":42267615,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37988]"}, {"versioned_ensembl_gene_id":"ENSG00000224806.2","gene_symbol":"ARL5AP4","gene_name":"ADP ribosylation factor like GTPase 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641379","summary":null,"start":24686168,"end":24686679,"strand":1,"description":"ADP ribosylation factor like GTPase 5A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43936]"}, {"versioned_ensembl_gene_id":"ENSG00000248796.1","gene_symbol":"MED15P8","gene_name":"mediator complex subunit 15 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48657]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480229","summary":null,"start":131201142,"end":131202941,"strand":-1,"description":"mediator complex subunit 15 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48657]"}, {"versioned_ensembl_gene_id":"ENSG00000281657.2","gene_symbol":"LINC00976","gene_name":"long intergenic non-protein coding RNA 976 [Source:NCBI gene;Acc:106144608]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144608","summary":null,"start":128904773,"end":128966001,"strand":-1,"description":"long intergenic non-protein coding RNA 976 [Source:NCBI gene;Acc:106144608]"}, {"versioned_ensembl_gene_id":"ENSG00000100276.9","gene_symbol":"RASL10A","gene_name":"RAS like family 10 member A [Source:HGNC Symbol;Acc:HGNC:16954]","synonyms":"RRP22","biotype":"protein_coding","ncbi_id":"10633","summary":null,"start":29312933,"end":29319679,"strand":-1,"description":"RAS like family 10 member A [Source:HGNC Symbol;Acc:HGNC:16954]"}, {"versioned_ensembl_gene_id":"ENSG00000273216.1","gene_symbol":"AC002059.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29316744,"end":29317220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253329.1","gene_symbol":"IGLV3-30","gene_name":"immunoglobulin lambda variable 3-30 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5912]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28789","summary":null,"start":22618572,"end":22619163,"strand":1,"description":"immunoglobulin lambda variable 3-30 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5912]"}, {"versioned_ensembl_gene_id":"ENSG00000235929.1","gene_symbol":"TPT1P14","gene_name":"tumor protein, translationally-controlled 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49305]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128521","summary":null,"start":14977959,"end":14978463,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49305]"}, {"versioned_ensembl_gene_id":"ENSG00000253120.1","gene_symbol":"IGLV2-34","gene_name":"immunoglobulin lambda variable 2-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5893]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28810","summary":null,"start":22580014,"end":22580296,"strand":1,"description":"immunoglobulin lambda variable 2-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5893]"}, {"versioned_ensembl_gene_id":"ENSG00000231255.1","gene_symbol":"AC005009.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86775081,"end":86776022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233073.1","gene_symbol":"AC005009.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86784226,"end":86786670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229224.1","gene_symbol":"AC105398.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29096843,"end":29097525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258652.3","gene_symbol":"OR4Q1P","gene_name":"olfactory receptor family 4 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15376]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81104","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22044496,"end":22045399,"strand":1,"description":"olfactory receptor family 4 subfamily Q member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15376]"}, {"versioned_ensembl_gene_id":"ENSG00000248099.3","gene_symbol":"INSL3","gene_name":"insulin like 3 [Source:HGNC Symbol;Acc:HGNC:6086]","synonyms":"RLNL,RLF,MGC119819,MGC119818","biotype":"protein_coding","ncbi_id":"3640","summary":"This gene encodes a member of the insulin-like hormone superfamily. The encoded protein is mainly produced in gonadal tissues. Studies of the mouse counterpart suggest that this gene may be involved in the development of urogenital tract and female fertility. This protein may also act as a hormone to regulate growth and differentiation of gubernaculum, and thus mediating intra-abdominal testicular descent. Mutations in this gene may lead to cryptorchidism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":17816512,"end":17821574,"strand":-1,"description":"insulin like 3 [Source:HGNC Symbol;Acc:HGNC:6086]"}, {"versioned_ensembl_gene_id":"ENSG00000144395.17","gene_symbol":"CCDC150","gene_name":"coiled-coil domain containing 150 [Source:HGNC Symbol;Acc:HGNC:26834]","synonyms":"FLJ39660","biotype":"protein_coding","ncbi_id":"284992","summary":null,"start":196639554,"end":196763490,"strand":1,"description":"coiled-coil domain containing 150 [Source:HGNC Symbol;Acc:HGNC:26834]"}, {"versioned_ensembl_gene_id":"ENSG00000283613.1","gene_symbol":"AC090897.3","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":54412763,"end":54424632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226838.1","gene_symbol":"AC096582.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45816557,"end":45821064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251378.1","gene_symbol":"AC096582.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45818582,"end":45819097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275245.1","gene_symbol":"GU182354.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54786437,"end":54797952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104976.11","gene_symbol":"SNAPC2","gene_name":"small nuclear RNA activating complex polypeptide 2 [Source:HGNC Symbol;Acc:HGNC:11135]","synonyms":"SNAP45,PTFdelta","biotype":"protein_coding","ncbi_id":"6618","summary":"This gene encodes a subunit of the snRNA-activating protein complex which is associated with the TATA box-binding protein. The encoded protein is necessary for RNA polymerase II and III dependent small-nuclear RNA gene transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]","start":7920316,"end":7923250,"strand":1,"description":"small nuclear RNA activating complex polypeptide 2 [Source:HGNC Symbol;Acc:HGNC:11135]"}, {"versioned_ensembl_gene_id":"ENSG00000115541.10","gene_symbol":"HSPE1","gene_name":"heat shock protein family E (Hsp10) member 1 [Source:HGNC Symbol;Acc:HGNC:5269]","synonyms":"HSP10,GroES,EPF,CPN10","biotype":"protein_coding","ncbi_id":"3336","summary":"This gene encodes a major heat shock protein which functions as a chaperonin. Its structure consists of a heptameric ring which binds to another heat shock protein in order to form a symmetric, functional heterodimer which enhances protein folding in an ATP-dependent manner. This gene and its co-chaperonin, HSPD1, are arranged in a head-to-head orientation on chromosome 2. Naturally occurring read-through transcription occurs between this locus and the neighboring locus MOBKL3.[provided by RefSeq, Feb 2011]","start":197499994,"end":197503457,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 [Source:HGNC Symbol;Acc:HGNC:5269]"}, {"versioned_ensembl_gene_id":"ENSG00000233472.1","gene_symbol":"AL390866.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27999788,"end":28049615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226395.1","gene_symbol":"MRPS21P5","gene_name":"mitochondrial ribosomal protein S21 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359769","summary":null,"start":28004702,"end":28004932,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29752]"}, {"versioned_ensembl_gene_id":"ENSG00000269837.1","gene_symbol":"IPO5P1","gene_name":"importin 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49687]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100132815","summary":null,"start":23255053,"end":23257939,"strand":-1,"description":"importin 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49687]"}, {"versioned_ensembl_gene_id":"ENSG00000196081.9","gene_symbol":"ZNF724","gene_name":"zinc finger protein 724 [Source:HGNC Symbol;Acc:HGNC:32460]","synonyms":"ZNF724P","biotype":"protein_coding","ncbi_id":"440519","summary":null,"start":23221599,"end":23250390,"strand":-1,"description":"zinc finger protein 724 [Source:HGNC Symbol;Acc:HGNC:32460]"}, {"versioned_ensembl_gene_id":"ENSG00000205882.8","gene_symbol":"DEFB134","gene_name":"defensin beta 134 [Source:HGNC Symbol;Acc:HGNC:32399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"613211","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 8p23. [provided by RefSeq, Nov 2014]","start":11993174,"end":11996312,"strand":-1,"description":"defensin beta 134 [Source:HGNC Symbol;Acc:HGNC:32399]"}, {"versioned_ensembl_gene_id":"ENSG00000127561.14","gene_symbol":"SYNGR3","gene_name":"synaptogyrin 3 [Source:HGNC Symbol;Acc:HGNC:11501]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9143","summary":"This gene encodes an integral membrane protein. The exact function of this protein is unclear, but studies of a similar murine protein suggest that it is a synaptic vesicle protein that also interacts with the dopamine transporter. The gene product belongs to the synaptogyrin gene family. [provided by RefSeq, Dec 2010]","start":1989660,"end":1994275,"strand":1,"description":"synaptogyrin 3 [Source:HGNC Symbol;Acc:HGNC:11501]"}, {"versioned_ensembl_gene_id":"ENSG00000248221.1","gene_symbol":"STX18-IT1","gene_name":"STX18 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41415]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"104472519","summary":null,"start":4476121,"end":4481700,"strand":-1,"description":"STX18 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41415]"}, {"versioned_ensembl_gene_id":"ENSG00000259521.1","gene_symbol":"INO80-AS1","gene_name":"INO80 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53138]","synonyms":"ENST00000560178","biotype":"antisense_RNA","ncbi_id":"109729177","summary":null,"start":41016807,"end":41027893,"strand":1,"description":"INO80 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53138]"}, {"versioned_ensembl_gene_id":"ENSG00000144481.16","gene_symbol":"TRPM8","gene_name":"transient receptor potential cation channel subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:17961]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79054","summary":null,"start":233917398,"end":234019522,"strand":1,"description":"transient receptor potential cation channel subfamily M member 8 [Source:HGNC Symbol;Acc:HGNC:17961]"}, {"versioned_ensembl_gene_id":"ENSG00000237581.1","gene_symbol":"AC005538.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":233946146,"end":233955435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149792.8","gene_symbol":"MRPL49","gene_name":"mitochondrial ribosomal protein L49 [Source:HGNC Symbol;Acc:HGNC:1176]","synonyms":"NOF1,NOF,L49mt,C11orf4","biotype":"protein_coding","ncbi_id":"740","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. Pseudogenes corresponding to this gene are found on chromosomes 5q and 8p. [provided by RefSeq, May 2011]","start":65122183,"end":65127371,"strand":1,"description":"mitochondrial ribosomal protein L49 [Source:HGNC Symbol;Acc:HGNC:1176]"}, {"versioned_ensembl_gene_id":"ENSG00000228919.5","gene_symbol":"AC097381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7939001,"end":7940296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263065.1","gene_symbol":"AF001548.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15741151,"end":15741791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174748.18","gene_symbol":"RPL15","gene_name":"ribosomal protein L15 [Source:HGNC Symbol;Acc:HGNC:10306]","synonyms":"RPYL10,RPLY10,RPL10,L15,EC45","biotype":"protein_coding","ncbi_id":"6138","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L15E family of ribosomal proteins and a component of the 60S subunit. This gene shares sequence similarity with the yeast ribosomal protein YL10 gene. Elevated expression of this gene has been observed in esophageal tumors and gastric cancer tissues, and deletion of this gene has been observed in a Diamond-Blackfan anemia (DBA) patient. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Mar 2017]","start":23916545,"end":23923692,"strand":1,"description":"ribosomal protein L15 [Source:HGNC Symbol;Acc:HGNC:10306]"}, {"versioned_ensembl_gene_id":"ENSG00000235952.1","gene_symbol":"AL845454.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29931441,"end":29932433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206014.7","gene_symbol":"OR7E161P","gene_name":"olfactory receptor family 7 subfamily E member 161 pseudogene [Source:HGNC Symbol;Acc:HGNC:31234]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"389626","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":11928597,"end":11933203,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 161 pseudogene [Source:HGNC Symbol;Acc:HGNC:31234]"}, {"versioned_ensembl_gene_id":"ENSG00000274319.1","gene_symbol":"RPSAP73","gene_name":"ribosomal protein SA pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:51926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075250","summary":null,"start":6365441,"end":6365770,"strand":1,"description":"ribosomal protein SA pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:51926]"}, {"versioned_ensembl_gene_id":"ENSG00000214917.3","gene_symbol":"AC011825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32075885,"end":32076272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261416.1","gene_symbol":"AC012645.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30183505,"end":30184957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136378.14","gene_symbol":"ADAMTS7","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 7 [Source:HGNC Symbol;Acc:HGNC:223]","synonyms":"ADAM-TS7,DKFZp434H204","biotype":"protein_coding","ncbi_id":"11173","summary":"The protein encoded by this gene is a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family. Members of this family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme contains two C-terminal TS motifs and may regulate vascular smooth muscle cell (VSMC) migration. Mutations in this gene may be associated with susceptibility to coronary artery disease. [provided by RefSeq, Feb 2016]","start":78759203,"end":78811431,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 7 [Source:HGNC Symbol;Acc:HGNC:223]"}, {"versioned_ensembl_gene_id":"ENSG00000174738.12","gene_symbol":"NR1D2","gene_name":"nuclear receptor subfamily 1 group D member 2 [Source:HGNC Symbol;Acc:HGNC:7963]","synonyms":"HZF2,Hs.37288,EAR-1r,BD73,RVR","biotype":"protein_coding","ncbi_id":"9975","summary":"This gene encodes a member of the nuclear hormone receptor family, specifically the NR1 subfamily of receptors. The encoded protein functions as a transcriptional repressor and may play a role in circadian rhythms and carbohydrate and lipid metabolism. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":23945260,"end":23980618,"strand":1,"description":"nuclear receptor subfamily 1 group D member 2 [Source:HGNC Symbol;Acc:HGNC:7963]"}, {"versioned_ensembl_gene_id":"ENSG00000279925.1","gene_symbol":"AC144522.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":110744549,"end":110746206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205754.10","gene_symbol":"SLCO1B7","gene_name":"solute carrier organic anion transporter family member 1B7 (putative) [Source:HGNC Symbol;Acc:HGNC:32934]","synonyms":"SLC21A21,LST3","biotype":"protein_coding","ncbi_id":"338821","summary":null,"start":21015696,"end":21092745,"strand":1,"description":"solute carrier organic anion transporter family member 1B7 (putative) [Source:HGNC Symbol;Acc:HGNC:32934]"}, {"versioned_ensembl_gene_id":"ENSG00000239718.1","gene_symbol":"HLTF-AS1","gene_name":"HLTF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40554]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873945","summary":null,"start":149086332,"end":149102823,"strand":1,"description":"HLTF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40554]"}, {"versioned_ensembl_gene_id":"ENSG00000163273.3","gene_symbol":"NPPC","gene_name":"natriuretic peptide C [Source:HGNC Symbol;Acc:HGNC:7941]","synonyms":"CNP","biotype":"protein_coding","ncbi_id":"4880","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include the cardiac natriuretic peptides CNP-53, CNP-29 and CNP-22, which belong to the natriuretic family of peptides. The encoded peptides exhibit vasorelaxation activity in laboratory animals and elevated levels of CNP-22 have been observed in the plasma of chronic heart failure patients. [provided by RefSeq, Oct 2015]","start":231921820,"end":231926403,"strand":-1,"description":"natriuretic peptide C [Source:HGNC Symbol;Acc:HGNC:7941]"}, {"versioned_ensembl_gene_id":"ENSG00000261096.1","gene_symbol":"AC073476.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":231809846,"end":231812352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174448.8","gene_symbol":"STARD6","gene_name":"StAR related lipid transfer domain containing 6 [Source:HGNC Symbol;Acc:HGNC:18066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147323","summary":"Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD6 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008]","start":54324358,"end":54357964,"strand":-1,"description":"StAR related lipid transfer domain containing 6 [Source:HGNC Symbol;Acc:HGNC:18066]"}, {"versioned_ensembl_gene_id":"ENSG00000275151.1","gene_symbol":"AC025771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29113759,"end":29114317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206505.13","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29930625,"end":29999286,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000233406.5","gene_symbol":"AL162430.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51250603,"end":51251472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278738.5","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"CD158A,47.11,p58.1,nkat1,cl-42","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54701102,"end":54715618,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000281687.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000259405.1","gene_symbol":"AC020661.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40948736,"end":40948869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276777.1","gene_symbol":"ARMC4P1","gene_name":"armadillo repeat containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060171","summary":null,"start":27288669,"end":27288857,"strand":1,"description":"armadillo repeat containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44937]"}, {"versioned_ensembl_gene_id":"ENSG00000228886.1","gene_symbol":"AL138963.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45350323,"end":45351350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214455.4","gene_symbol":"RCN1P2","gene_name":"reticulocalbin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39204]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728913","summary":null,"start":45390353,"end":45391267,"strand":-1,"description":"reticulocalbin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39204]"}, {"versioned_ensembl_gene_id":"ENSG00000261108.2","gene_symbol":"AC138907.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32739627,"end":32740166,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125648.14","gene_symbol":"SLC25A23","gene_name":"solute carrier family 25 member 23 [Source:HGNC Symbol;Acc:HGNC:19375]","synonyms":"MGC2615,FLJ30339,APC2","biotype":"protein_coding","ncbi_id":"79085","summary":null,"start":6436079,"end":6465203,"strand":-1,"description":"solute carrier family 25 member 23 [Source:HGNC Symbol;Acc:HGNC:19375]"}, {"versioned_ensembl_gene_id":"ENSG00000281313.1","gene_symbol":"OR5G1P","gene_name":"olfactory receptor family 5 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8344]","synonyms":"OR93,OR5G2P,OR11-104","biotype":"unprocessed_pseudogene","ncbi_id":"8591","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56786335,"end":56787280,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8344]"}, {"versioned_ensembl_gene_id":"ENSG00000231854.1","gene_symbol":"BX927194.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30884177,"end":30892811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176595.3","gene_symbol":"KBTBD11","gene_name":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]","synonyms":"KLHDC7C,KIAA0711","biotype":"protein_coding","ncbi_id":"9920","summary":null,"start":1973878,"end":2006936,"strand":1,"description":"kelch repeat and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:29104]"}, {"versioned_ensembl_gene_id":"ENSG00000281777.1","gene_symbol":"OR9G2P","gene_name":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]","synonyms":"OR9G6","biotype":"unprocessed_pseudogene","ncbi_id":"81160","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56762097,"end":56762976,"strand":-1,"description":"olfactory receptor family 9 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15320]"}, {"versioned_ensembl_gene_id":"ENSG00000174938.14","gene_symbol":"SEZ6L2","gene_name":"seizure related 6 homolog like 2 [Source:HGNC Symbol;Acc:HGNC:30844]","synonyms":"PSK-1,FLJ90517","biotype":"protein_coding","ncbi_id":"26470","summary":"This gene encodes a seizure-related protein that is localized on the cell surface. The gene is located in a region of chromosome 16p11.2 that is thought to contain candidate genes for autism spectrum disorders (ASD), though there is no evidence directly implicating this gene in ASD. Increased expression of this gene has been found in lung cancers, and the protein is therefore considered to be a novel prognostic marker for lung cancer. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":29871159,"end":29899547,"strand":-1,"description":"seizure related 6 homolog like 2 [Source:HGNC Symbol;Acc:HGNC:30844]"}, {"versioned_ensembl_gene_id":"ENSG00000277040.1","gene_symbol":"AL359736.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24323021,"end":24323457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232309.1","gene_symbol":"AL390856.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182127297,"end":182128665,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180053.7","gene_symbol":"NKX2-6","gene_name":"NK2 homeobox 6 [Source:HGNC Symbol;Acc:HGNC:32940]","synonyms":"NKX4-2,CSX2","biotype":"protein_coding","ncbi_id":"137814","summary":"This gene encodes a homeobox-containing protein that belongs to the NK-2 homeobox family. This protein is a vertebrate homolog of Drosophila homeobox-containing protein called 'tinman', which has been shown to be essential for development of the heart-like dorsal vessel. In conjunction with related gene, NKX2-5, this gene may play a role in both pharyngeal and cardiac embryonic development. Mutations in this gene are associated with persistent truncus arteriosus.[provided by RefSeq, Aug 2011]","start":23702451,"end":23706598,"strand":-1,"description":"NK2 homeobox 6 [Source:HGNC Symbol;Acc:HGNC:32940]"}, {"versioned_ensembl_gene_id":"ENSG00000182165.17","gene_symbol":"TP53TG1","gene_name":"TP53 target 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17026]","synonyms":"TP53AP1,LINC00096,H_RG012D21.9","biotype":"lincRNA","ncbi_id":"11257","summary":null,"start":87325225,"end":87345515,"strand":-1,"description":"TP53 target 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17026]"}, {"versioned_ensembl_gene_id":"ENSG00000251062.1","gene_symbol":"AC025459.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32887990,"end":32888145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258090.1","gene_symbol":"AC093014.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76757191,"end":76757914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238193.1","gene_symbol":"AC112656.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5305714,"end":5307128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254532.1","gene_symbol":"AC124657.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30044058,"end":30084343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234944.1","gene_symbol":"AL365199.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42871521,"end":42874060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257526.2","gene_symbol":"AC107032.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76562294,"end":76615567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168000.14","gene_symbol":"BSCL2","gene_name":"BSCL2, seipin lipid droplet biogenesis associated [Source:HGNC Symbol;Acc:HGNC:15832]","synonyms":"SPG17,GNG3LG","biotype":"protein_coding","ncbi_id":"26580","summary":"This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).[provided by RefSeq, Mar 2011]","start":62690275,"end":62709845,"strand":-1,"description":"BSCL2, seipin lipid droplet biogenesis associated [Source:HGNC Symbol;Acc:HGNC:15832]"}, {"versioned_ensembl_gene_id":"ENSG00000179930.5","gene_symbol":"ZNF648","gene_name":"zinc finger protein 648 [Source:HGNC Symbol;Acc:HGNC:18190]","synonyms":"FLJ46813","biotype":"protein_coding","ncbi_id":"127665","summary":null,"start":182054570,"end":182061712,"strand":-1,"description":"zinc finger protein 648 [Source:HGNC Symbol;Acc:HGNC:18190]"}, {"versioned_ensembl_gene_id":"ENSG00000214753.2","gene_symbol":"HNRNPUL2","gene_name":"heterogeneous nuclear ribonucleoprotein U like 2 [Source:HGNC Symbol;Acc:HGNC:25451]","synonyms":"HNRPUL2,DKFZp762N1910","biotype":"protein_coding","ncbi_id":"221092","summary":null,"start":62712630,"end":62727349,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein U like 2 [Source:HGNC Symbol;Acc:HGNC:25451]"}, {"versioned_ensembl_gene_id":"ENSG00000274798.1","gene_symbol":"AC025166.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40874433,"end":40874595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240809.1","gene_symbol":"AC026877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76434018,"end":76435428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260947.1","gene_symbol":"AL356489.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33697459,"end":33700986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214650.2","gene_symbol":"AC073592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124513222,"end":124514813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181626.11","gene_symbol":"ANKRD62","gene_name":"ankyrin repeat domain 62 [Source:HGNC Symbol;Acc:HGNC:35241]","synonyms":"DKFZp779B1634","biotype":"protein_coding","ncbi_id":"342850","summary":null,"start":12093853,"end":12129749,"strand":1,"description":"ankyrin repeat domain 62 [Source:HGNC Symbol;Acc:HGNC:35241]"}, {"versioned_ensembl_gene_id":"ENSG00000168582.4","gene_symbol":"CRYGA","gene_name":"crystallin gamma A [Source:HGNC Symbol;Acc:HGNC:2408]","synonyms":"CRYG5,CRYG1,CRY-g-A","biotype":"protein_coding","ncbi_id":"1418","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. Four gamma-crystallin genes (gamma-A through gamma-D) and three pseudogenes (gamma-E, gamma-F, gamma-G) are tandemly organized in a genomic segment as a gene cluster. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation. [provided by RefSeq, Jul 2008]","start":208160740,"end":208163576,"strand":-1,"description":"crystallin gamma A [Source:HGNC Symbol;Acc:HGNC:2408]"}, {"versioned_ensembl_gene_id":"ENSG00000185164.14","gene_symbol":"NOMO2","gene_name":"NODAL modulator 2 [Source:HGNC Symbol;Acc:HGNC:22652]","synonyms":"NOMO,PM5","biotype":"protein_coding","ncbi_id":"283820","summary":"This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a region of duplication located on the p arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum (PXE). Two transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":18417325,"end":18562211,"strand":-1,"description":"NODAL modulator 2 [Source:HGNC Symbol;Acc:HGNC:22652]"}, {"versioned_ensembl_gene_id":"ENSG00000270988.1","gene_symbol":"AC019257.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1974818,"end":1975314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107099.15","gene_symbol":"DOCK8","gene_name":"dedicator of cytokinesis 8 [Source:HGNC Symbol;Acc:HGNC:19191]","synonyms":"ZIR8,FLJ00346,FLJ00152,FLJ00026","biotype":"protein_coding","ncbi_id":"81704","summary":"This gene encodes a member of the DOCK180 family of guanine nucleotide exchange factors. Guanine nucleotide exchange factors interact with Rho GTPases and are components of intracellular signaling networks. Mutations in this gene result in the autosomal recessive form of the hyper-IgE syndrome. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Jun 2010]","start":214854,"end":465259,"strand":1,"description":"dedicator of cytokinesis 8 [Source:HGNC Symbol;Acc:HGNC:19191]"}, {"versioned_ensembl_gene_id":"ENSG00000280395.1","gene_symbol":"AL034546.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":50092745,"end":50096437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101292.7","gene_symbol":"PROKR2","gene_name":"prokineticin receptor 2 [Source:HGNC Symbol;Acc:HGNC:15836]","synonyms":"PKR2,KAL3,GPRg2,GPR73L1,GPR73b,dJ680N4.3","biotype":"protein_coding","ncbi_id":"128674","summary":"Prokineticins are secreted proteins that can promote angiogenesis and induce strong gastrointestinal smooth muscle contraction. The protein encoded by this gene is an integral membrane protein and G protein-coupled receptor for prokineticins. The encoded protein is similar in sequence to GPR73, another G protein-coupled receptor for prokineticins. [provided by RefSeq, Jul 2008]","start":5302040,"end":5314369,"strand":-1,"description":"prokineticin receptor 2 [Source:HGNC Symbol;Acc:HGNC:15836]"}, {"versioned_ensembl_gene_id":"ENSG00000226603.8","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"G6D,MEGT1,C6orf23,Ly6-D,NG25","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31694313,"end":31705325,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000229994.1","gene_symbol":"RPL5P4","gene_name":"ribosomal protein L5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36095]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643343","summary":null,"start":35350722,"end":35351607,"strand":1,"description":"ribosomal protein L5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36095]"}, {"versioned_ensembl_gene_id":"ENSG00000281128.1","gene_symbol":"PTENP1-AS","gene_name":"PTENP1 antisense RNA [Source:NCBI gene;Acc:101243555]","synonyms":"PTENpg1-asRNA,PTENP1as","biotype":"antisense_RNA","ncbi_id":"101243555","summary":"PTENP1-AS encodes an antisense RNA (asRNA) of PTENP1, a PTEN (phosphatase and tensin homolog) pseudogene. PTENP1 regulates PTEN by both sense (GeneID: 11191) and antisense RNAs. This antisense RNA (PTENP1-AS) regulates PTEN transcription and mRNA stability. [provided by RefSeq, Jun 2020]","start":33677268,"end":33688011,"strand":1,"description":"PTENP1 antisense RNA [Source:NCBI gene;Acc:101243555]"}, {"versioned_ensembl_gene_id":"ENSG00000179420.11","gene_symbol":"OR6W1P","gene_name":"olfactory receptor family 6 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15091]","synonyms":"sdolf,OR6W1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"89883","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143062330,"end":143063585,"strand":-1,"description":"olfactory receptor family 6 subfamily W member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15091]"}, {"versioned_ensembl_gene_id":"ENSG00000185038.14","gene_symbol":"MROH2A","gene_name":"maestro heat like repeat family member 2A [Source:HGNC Symbol;Acc:HGNC:27936]","synonyms":"HEATR7B1","biotype":"protein_coding","ncbi_id":"339766","summary":"This gene encodes a HEAT-domain-containing protein. The function of the encoded protein has not been characterized. [provided by RefSeq, Aug 2016]","start":233775679,"end":233833423,"strand":1,"description":"maestro heat like repeat family member 2A [Source:HGNC Symbol;Acc:HGNC:27936]"}, {"versioned_ensembl_gene_id":"ENSG00000260307.2","gene_symbol":"AC138915.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32439069,"end":32441159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255361.1","gene_symbol":"AC103843.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42725547,"end":42726228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228605.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31651971,"end":31657032,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000229064.1","gene_symbol":"AC104073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65247608,"end":65247758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183938.5","gene_symbol":"TRBV21OR9-2","gene_name":"T-cell receptor beta variable 21/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12199]","synonyms":"TRBV21/OR9-2,TCRBV21S2,TCRBV10S2O,TCRBV10O","biotype":"TR_V_gene","ncbi_id":"6959","summary":null,"start":33629121,"end":33629586,"strand":1,"description":"T-cell receptor beta variable 21/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12199]"}, {"versioned_ensembl_gene_id":"ENSG00000265477.1","gene_symbol":"AP000915.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":423744,"end":424416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264514.1","gene_symbol":"AP000915.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":316737,"end":319165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230699.2","gene_symbol":"AL645608.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":911435,"end":914948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196911.10","gene_symbol":"KPNA5","gene_name":"karyopherin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6398]","synonyms":"SRP6,IPOA6","biotype":"protein_coding","ncbi_id":"3841","summary":"The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC) which consists of 60-100 proteins and is probably 120 million daltons in molecular size. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion; larger molecules are transported by an active process. Most nuclear proteins contain short basic amino acid sequences known as nuclear localization signals (NLSs). KPNA5 protein belongs to the importin alpha protein family and is thought to be involved in NLS-dependent protein import into the nucleus. [provided by RefSeq, Jul 2008]","start":116681187,"end":116741866,"strand":1,"description":"karyopherin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6398]"}, {"versioned_ensembl_gene_id":"ENSG00000279856.1","gene_symbol":"AC106733.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77104260,"end":77105297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240868.1","gene_symbol":"C1QTNF9-AS1","gene_name":"C1QTNF9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39906]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874232","summary":null,"start":24315725,"end":24321598,"strand":-1,"description":"C1QTNF9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39906]"}, {"versioned_ensembl_gene_id":"ENSG00000231925.11","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33299694,"end":33314387,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000260455.1","gene_symbol":"NBAT1","gene_name":"neuroblastoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:49075]","synonyms":"NBAT-1,CASC14","biotype":"lincRNA","ncbi_id":"729177","summary":null,"start":22134957,"end":22147193,"strand":-1,"description":"neuroblastoma associated transcript 1 [Source:HGNC Symbol;Acc:HGNC:49075]"}, {"versioned_ensembl_gene_id":"ENSG00000133460.19","gene_symbol":"SLC2A11","gene_name":"solute carrier family 2 member 11 [Source:HGNC Symbol;Acc:HGNC:14239]","synonyms":"GLUT11,GLUT10","biotype":"protein_coding","ncbi_id":"66035","summary":"This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":23856703,"end":23886309,"strand":1,"description":"solute carrier family 2 member 11 [Source:HGNC Symbol;Acc:HGNC:14239]"}, {"versioned_ensembl_gene_id":"ENSG00000275619.2","gene_symbol":"GON7","gene_name":"GON7, KEOPS complex subunit homolog [Source:HGNC Symbol;Acc:HGNC:20356]","synonyms":"C14orf142","biotype":"protein_coding","ncbi_id":"84520","summary":null,"start":93202894,"end":93207094,"strand":-1,"description":"GON7, KEOPS complex subunit homolog [Source:HGNC Symbol;Acc:HGNC:20356]"}, {"versioned_ensembl_gene_id":"ENSG00000278555.4","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"CD85k,LIR-5,ILT3,HM18,LIR5","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54594151,"end":54602395,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000173457.10","gene_symbol":"PPP1R14B","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14B [Source:HGNC Symbol;Acc:HGNC:9057]","synonyms":"SOM172,PNG,PLCB3N,PHI-1","biotype":"protein_coding","ncbi_id":"26472","summary":null,"start":64244480,"end":64246941,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14B [Source:HGNC Symbol;Acc:HGNC:9057]"}, {"versioned_ensembl_gene_id":"ENSG00000227113.2","gene_symbol":"AC073210.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65075023,"end":65078780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006327.13","gene_symbol":"TNFRSF12A","gene_name":"TNF receptor superfamily member 12A [Source:HGNC Symbol;Acc:HGNC:18152]","synonyms":"TweakR,FN14,CD266","biotype":"protein_coding","ncbi_id":"51330","summary":null,"start":3018445,"end":3022383,"strand":1,"description":"TNF receptor superfamily member 12A [Source:HGNC Symbol;Acc:HGNC:18152]"}, {"versioned_ensembl_gene_id":"ENSG00000228072.1","gene_symbol":"AL139008.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33512959,"end":33514773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167723.14","gene_symbol":"TRPV3","gene_name":"transient receptor potential cation channel subfamily V member 3 [Source:HGNC Symbol;Acc:HGNC:18084]","synonyms":"VRL3","biotype":"protein_coding","ncbi_id":"162514","summary":"This gene product belongs to a family of nonselective cation channels that function in a variety of processes, including temperature sensation and vasoregulation. The thermosensitive members of this family are expressed in subsets of sensory neurons that terminate in the skin, and are activated at distinct physiological temperatures. This channel is activated at temperatures between 22 and 40 degrees C. This gene lies in close proximity to another family member gene on chromosome 17, and the two encoded proteins are thought to associate with each other to form heteromeric channels. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":3510502,"end":3557995,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 3 [Source:HGNC Symbol;Acc:HGNC:18084]"}, {"versioned_ensembl_gene_id":"ENSG00000103653.16","gene_symbol":"CSK","gene_name":"C-terminal Src kinase [Source:HGNC Symbol;Acc:HGNC:2444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1445","summary":"The protein encoded by this gene is involved in multiple pathways, including the regulation of Src family kinases. It plays an important role in T-cell activation through its association with the protein encoded by the protein tyrosine phosphatase, non-receptor type 22 (PTPN22) gene. This protein also phosphorylates C-terminal tyrosine residues on multiple substrates, including the protein encoded by the SRC proto-oncogene, non-receptor tyrosine kinase gene. Phosphorylation suppresses the kinase activity of the Src family tyrosine kinases. An intronic polymorphism (rs34933034) in this gene has been found to affect B-cell activation and is associated with systemic lupus erythematosus (SLE). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]","start":74782057,"end":74803198,"strand":1,"description":"C-terminal Src kinase [Source:HGNC Symbol;Acc:HGNC:2444]"}, {"versioned_ensembl_gene_id":"ENSG00000106648.13","gene_symbol":"GALNTL5","gene_name":"polypeptide N-acetylgalactosaminyltransferase like 5 [Source:HGNC Symbol;Acc:HGNC:21725]","synonyms":"GALNT15,GalNAc-T5L","biotype":"protein_coding","ncbi_id":"168391","summary":null,"start":151956379,"end":152019934,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase like 5 [Source:HGNC Symbol;Acc:HGNC:21725]"}, {"versioned_ensembl_gene_id":"ENSG00000160949.16","gene_symbol":"TONSL","gene_name":"tonsoku like, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:7801]","synonyms":"NFKBIL2,IKBR","biotype":"protein_coding","ncbi_id":"4796","summary":"The protein encoded by this gene is thought to be a negative regulator of NF-kappa-B mediated transcription. The encoded protein may bind NF-kappa-B complexes and trap them in the cytoplasm, preventing them from entering the nucleus and interacting with the DNA. Phosphorylation of this protein targets it for degradation by the ubiquitination pathway, which frees the NF-kappa-B complexes to enter the nucleus. [provided by RefSeq, Jul 2008]","start":144428775,"end":144444444,"strand":-1,"description":"tonsoku like, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:7801]"}, {"versioned_ensembl_gene_id":"ENSG00000276384.1","gene_symbol":"AC016876.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7557820,"end":7558245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237990.3","gene_symbol":"CNTN4-AS1","gene_name":"CNTN4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39985]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873975","summary":null,"start":3039033,"end":3069242,"strand":-1,"description":"CNTN4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39985]"}, {"versioned_ensembl_gene_id":"ENSG00000274762.1","gene_symbol":"AL049777.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28818741,"end":28819258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227720.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"CFAP255,HCGV,Tctex5,HCG-V,TCTE5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30057032,"end":30060656,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000256654.3","gene_symbol":"AC005906.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":4909867,"end":5026012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276418.5","gene_symbol":"AC036214.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":79918860,"end":80080775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196114.3","gene_symbol":"AL031577.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34576258,"end":34576656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155792.9","gene_symbol":"DEPTOR","gene_name":"DEP domain containing MTOR interacting protein [Source:HGNC Symbol;Acc:HGNC:22953]","synonyms":"FLJ12428,DEPDC6,DEP.6","biotype":"protein_coding","ncbi_id":"64798","summary":null,"start":119873717,"end":120050913,"strand":1,"description":"DEP domain containing MTOR interacting protein [Source:HGNC Symbol;Acc:HGNC:22953]"}, {"versioned_ensembl_gene_id":"ENSG00000164828.17","gene_symbol":"SUN1","gene_name":"Sad1 and UNC84 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18587]","synonyms":"UNC84A,KIAA0810,FLJ12407","biotype":"protein_coding","ncbi_id":"23353","summary":"This gene is a member of the unc-84 homolog family and encodes a nuclear envelope protein with an Unc84 (SUN) domain. The protein is involved in nuclear anchorage and migration. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2019]","start":816615,"end":896435,"strand":1,"description":"Sad1 and UNC84 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18587]"}, {"versioned_ensembl_gene_id":"ENSG00000258932.5","gene_symbol":"AL390334.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":27258717,"end":27845286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237763.9","gene_symbol":"AMY1A","gene_name":"amylase, alpha 1A (salivary) [Source:HGNC Symbol;Acc:HGNC:474]","synonyms":"AMY1","biotype":"protein_coding","ncbi_id":"276","summary":"Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the salivary gland. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":103655290,"end":103664554,"strand":1,"description":"amylase, alpha 1A (salivary) [Source:HGNC Symbol;Acc:HGNC:474]"}, {"versioned_ensembl_gene_id":"ENSG00000254606.1","gene_symbol":"AC013714.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28516832,"end":28519341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274779.4","gene_symbol":"NOMO1","gene_name":"NODAL modulator 1 [Source:HGNC Symbol;Acc:HGNC:30060]","synonyms":"PM5","biotype":"protein_coding","ncbi_id":"23420","summary":"This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a region of duplication located on the p arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum (PXE). [provided by RefSeq, Jul 2008]","start":15317897,"end":15380303,"strand":-1,"description":"NODAL modulator 1 [Source:HGNC Symbol;Acc:HGNC:30060]"}, {"versioned_ensembl_gene_id":"ENSG00000262636.1","gene_symbol":"AC099489.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11380859,"end":11381118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180090.5","gene_symbol":"OR3A1","gene_name":"olfactory receptor family 3 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8282]","synonyms":"OR40,OR17-40,OLFRA03","biotype":"protein_coding","ncbi_id":"4994","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3291017,"end":3298360,"strand":-1,"description":"olfactory receptor family 3 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8282]"}, {"versioned_ensembl_gene_id":"ENSG00000237366.1","gene_symbol":"AL662857.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29259390,"end":29260766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174680.9","gene_symbol":"GRIK1-AS1","gene_name":"GRIK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16458]","synonyms":"GRIK1AS,GRIK1-AS,C21orf9,NCRNA00110","biotype":"antisense_RNA","ncbi_id":"642976","summary":null,"start":29748175,"end":29764002,"strand":1,"description":"GRIK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16458]"}, {"versioned_ensembl_gene_id":"ENSG00000234092.1","gene_symbol":"AL662857.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29211927,"end":29212864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160766.14","gene_symbol":"GBAP1","gene_name":"glucosylceramidase beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4178]","synonyms":"GBAP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"2630","summary":null,"start":155213821,"end":155227422,"strand":-1,"description":"glucosylceramidase beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4178]"}, {"versioned_ensembl_gene_id":"ENSG00000260846.2","gene_symbol":"FRG2HP","gene_name":"FSHD region gene 2 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51794]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101059920","summary":null,"start":35335277,"end":35336889,"strand":-1,"description":"FSHD region gene 2 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51794]"}, {"versioned_ensembl_gene_id":"ENSG00000167994.11","gene_symbol":"RAB3IL1","gene_name":"RAB3A interacting protein like 1 [Source:HGNC Symbol;Acc:HGNC:9780]","synonyms":"GRAB","biotype":"protein_coding","ncbi_id":"5866","summary":"This gene encodes a guanine nucleotide exchange factor for the ras-related protein Rab3A. The encoded protein binds Rab3a and the inositol hexakisphosphate kinase InsP6K1. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Nov 2012]","start":61897301,"end":61920269,"strand":-1,"description":"RAB3A interacting protein like 1 [Source:HGNC Symbol;Acc:HGNC:9780]"}, {"versioned_ensembl_gene_id":"ENSG00000271215.1","gene_symbol":"RPL21P136","gene_name":"ribosomal protein L21 pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:49854]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419521","summary":null,"start":12614359,"end":12615907,"strand":-1,"description":"ribosomal protein L21 pseudogene 136 [Source:HGNC Symbol;Acc:HGNC:49854]"}, {"versioned_ensembl_gene_id":"ENSG00000152926.14","gene_symbol":"ZNF117","gene_name":"zinc finger protein 117 [Source:HGNC Symbol;Acc:HGNC:12897]","synonyms":"H-plk,HPF9","biotype":"protein_coding","ncbi_id":"51351","summary":"This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Readthrough transcription occurs between this gene and the upstream endogenous retrovirus group 3 member 1 (ERV3-1) locus, and may result in additional transcript variants encoding the zinc finger protein. [provided by RefSeq, Jan 2017]","start":64971776,"end":65006684,"strand":-1,"description":"zinc finger protein 117 [Source:HGNC Symbol;Acc:HGNC:12897]"}, {"versioned_ensembl_gene_id":"ENSG00000260866.1","gene_symbol":"AC138915.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32388135,"end":32436200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126005.16","gene_symbol":"MMP24-AS1","gene_name":"MMP24 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44421]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101410538","summary":null,"start":35201745,"end":35278131,"strand":-1,"description":"MMP24 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44421]"}, {"versioned_ensembl_gene_id":"ENSG00000265158.1","gene_symbol":"LRRC37A7P","gene_name":"leucine rich repeat containing 37 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:43792]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100421589","summary":null,"start":31724198,"end":31726956,"strand":1,"description":"leucine rich repeat containing 37 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:43792]"}, {"versioned_ensembl_gene_id":"ENSG00000272478.1","gene_symbol":"AL020996.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25831913,"end":25832134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223732.2","gene_symbol":"AL359706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44982077,"end":45083125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179094.15","gene_symbol":"PER1","gene_name":"period circadian clock 1 [Source:HGNC Symbol;Acc:HGNC:8845]","synonyms":"RIGUI,PER","biotype":"protein_coding","ncbi_id":"5187","summary":"This gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene may increase the risk of getting certain cancers. Alternative splicing has been observed in this gene; however, these variants have not been fully described. [provided by RefSeq, Jan 2014]","start":8140472,"end":8156506,"strand":-1,"description":"period circadian clock 1 [Source:HGNC Symbol;Acc:HGNC:8845]"}, {"versioned_ensembl_gene_id":"ENSG00000275599.1","gene_symbol":"GU182352.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54843950,"end":54858409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235159.1","gene_symbol":"AL121672.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46067356,"end":46069891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241990.5","gene_symbol":"PRR34-AS1","gene_name":"PRR34 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50499]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"150381","summary":null,"start":46053705,"end":46057210,"strand":1,"description":"PRR34 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50499]"}, {"versioned_ensembl_gene_id":"ENSG00000232503.1","gene_symbol":"CYCSP8","gene_name":"cytochrome c, somatic pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:24423]","synonyms":"HCP8","biotype":"processed_pseudogene","ncbi_id":"360160","summary":null,"start":130776646,"end":130776957,"strand":1,"description":"cytochrome c, somatic pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:24423]"}, {"versioned_ensembl_gene_id":"ENSG00000213693.4","gene_symbol":"SEC14L1P1","gene_name":"SEC14 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44189]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729799","summary":null,"start":43897456,"end":43899636,"strand":1,"description":"SEC14 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44189]"}, {"versioned_ensembl_gene_id":"ENSG00000228993.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"dJ271M21.8,PsiGPR53","biotype":"unprocessed_pseudogene","ncbi_id":"9292","summary":null,"start":29537493,"end":29538576,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000088833.17","gene_symbol":"NSFL1C","gene_name":"NSFL1 cofactor [Source:HGNC Symbol;Acc:HGNC:15912]","synonyms":"dJ776F14.1,UBXN2C,UBXD10,UBX1,p47","biotype":"protein_coding","ncbi_id":"55968","summary":"N-ethylmaleimide-sensitive factor (NSF) and valosin-containing protein (p97) are two ATPases known to be involved in transport vesicle/target membrane fusion and fusions between membrane compartments. A trimer of the protein encoded by this gene binds a hexamer of cytosolic p97 and is required for p97-mediated regrowth of Golgi cisternae from mitotic Golgi fragments. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, May 2011]","start":1442162,"end":1473842,"strand":-1,"description":"NSFL1 cofactor [Source:HGNC Symbol;Acc:HGNC:15912]"}, {"versioned_ensembl_gene_id":"ENSG00000273335.1","gene_symbol":"AP005432.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9473421,"end":9474006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232188.1","gene_symbol":"AL354714.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160931739,"end":160934380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229797.1","gene_symbol":"AC140481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130743538,"end":130755879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237585.1","gene_symbol":"LINC00407","gene_name":"long intergenic non-protein coding RNA 407 [Source:HGNC Symbol;Acc:HGNC:42739]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144541","summary":null,"start":44651812,"end":44701016,"strand":1,"description":"long intergenic non-protein coding RNA 407 [Source:HGNC Symbol;Acc:HGNC:42739]"}, {"versioned_ensembl_gene_id":"ENSG00000213080.3","gene_symbol":"AL354714.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160894980,"end":160896076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206506.10","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29824140,"end":29828314,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000231711.2","gene_symbol":"LINC00899","gene_name":"long intergenic non-protein coding RNA 899 [Source:HGNC Symbol;Acc:HGNC:48583]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100271722","summary":null,"start":46039907,"end":46044853,"strand":-1,"description":"long intergenic non-protein coding RNA 899 [Source:HGNC Symbol;Acc:HGNC:48583]"}, {"versioned_ensembl_gene_id":"ENSG00000225023.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824558,"end":29825536,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000262435.1","gene_symbol":"AC215219.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14522,"end":32015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262890.1","gene_symbol":"AC027281.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70802083,"end":70802840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253752.1","gene_symbol":"IGLVI-63","gene_name":"immunoglobulin lambda variable (I)-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5938]","synonyms":"IGLV(I)-63","biotype":"IG_V_pseudogene","ncbi_id":"28765","summary":null,"start":22079770,"end":22080263,"strand":1,"description":"immunoglobulin lambda variable (I)-63 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5938]"}, {"versioned_ensembl_gene_id":"ENSG00000227710.1","gene_symbol":"AC245517.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22168289,"end":22168634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257927.1","gene_symbol":"MRPS36P5","gene_name":"mitochondrial ribosomal protein S36 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347703","summary":null,"start":43054089,"end":43054386,"strand":-1,"description":"mitochondrial ribosomal protein S36 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29775]"}, {"versioned_ensembl_gene_id":"ENSG00000257373.1","gene_symbol":"AC012038.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42979254,"end":42996486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116985.11","gene_symbol":"BMP8B","gene_name":"bone morphogenetic protein 8b [Source:HGNC Symbol;Acc:HGNC:1075]","synonyms":"OP-2,BMP8","biotype":"protein_coding","ncbi_id":"656","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The encoded protein stimulates thermogenesis in brown adipose tissue. Expression of this gene may be downregulated in pancreatic cancer. This gene may have arose from a gene duplication event and its gene duplicate is also present on chromosome 1. [provided by RefSeq, Jul 2016]","start":39757182,"end":39788861,"strand":-1,"description":"bone morphogenetic protein 8b [Source:HGNC Symbol;Acc:HGNC:1075]"}, {"versioned_ensembl_gene_id":"ENSG00000225333.6","gene_symbol":"AL035404.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39718028,"end":39718595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197549.9","gene_symbol":"PRAMENP","gene_name":"PRAME N-terminal-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:34302]","synonyms":"PRAMEL,PRAMEF24P,FLJ16327","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"649179","summary":null,"start":21991099,"end":22043934,"strand":-1,"description":"PRAME N-terminal-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:34302]"}, {"versioned_ensembl_gene_id":"ENSG00000262473.5","gene_symbol":"GART","gene_name":"phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Source:HGNC Symbol;Acc:HGNC:4163]","synonyms":"PGFT,PRGS","biotype":"protein_coding","ncbi_id":"2618","summary":"The protein encoded by this gene is a trifunctional polypeptide. It has phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase activity which is required for de novo purine biosynthesis. This enzyme is highly conserved in vertebrates. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33508081,"end":33521016,"strand":-1,"description":"phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Source:HGNC Symbol;Acc:HGNC:4163]"}, {"versioned_ensembl_gene_id":"ENSG00000211638.2","gene_symbol":"IGLV8-61","gene_name":"immunoglobulin lambda variable 8-61 [Source:HGNC Symbol;Acc:HGNC:5931]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28774","summary":null,"start":22098700,"end":22099212,"strand":1,"description":"immunoglobulin lambda variable 8-61 [Source:HGNC Symbol;Acc:HGNC:5931]"}, {"versioned_ensembl_gene_id":"ENSG00000163093.11","gene_symbol":"BBS5","gene_name":"Bardet-Biedl syndrome 5 [Source:HGNC Symbol;Acc:HGNC:970]","synonyms":"DKFZp762I194","biotype":"protein_coding","ncbi_id":"129880","summary":"This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized. [provided by RefSeq, Jul 2008]","start":169479178,"end":169506655,"strand":1,"description":"Bardet-Biedl syndrome 5 [Source:HGNC Symbol;Acc:HGNC:970]"}, {"versioned_ensembl_gene_id":"ENSG00000225741.1","gene_symbol":"AC245517.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22103219,"end":22104857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254308.1","gene_symbol":"IGLVIV-59","gene_name":"immunoglobulin lambda variable (IV)-59 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5942]","synonyms":"IGLV(IV)-59","biotype":"IG_V_pseudogene","ncbi_id":"28761","summary":null,"start":22179228,"end":22179477,"strand":1,"description":"immunoglobulin lambda variable (IV)-59 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5942]"}, {"versioned_ensembl_gene_id":"ENSG00000234851.4","gene_symbol":"RPL23AP42","gene_name":"ribosomal protein L23a pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:35942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647099","summary":null,"start":161429127,"end":161429597,"strand":-1,"description":"ribosomal protein L23a pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:35942]"}, {"versioned_ensembl_gene_id":"ENSG00000267314.1","gene_symbol":"AC104532.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5904841,"end":5914707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226652.3","gene_symbol":"PSMD10P2","gene_name":"proteasome 26S subunit, non-ATPase, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30151]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"280644","summary":null,"start":186760693,"end":186762050,"strand":1,"description":"proteasome 26S subunit, non-ATPase, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30151]"}, {"versioned_ensembl_gene_id":"ENSG00000258548.5","gene_symbol":"LINC00645","gene_name":"long intergenic non-protein coding RNA 645 [Source:HGNC Symbol;Acc:HGNC:44299]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505967","summary":null,"start":27612588,"end":27639636,"strand":1,"description":"long intergenic non-protein coding RNA 645 [Source:HGNC Symbol;Acc:HGNC:44299]"}, {"versioned_ensembl_gene_id":"ENSG00000129103.17","gene_symbol":"SUMF2","gene_name":"sulfatase modifying factor 2 [Source:HGNC Symbol;Acc:HGNC:20415]","synonyms":"DKFZp566I1024","biotype":"protein_coding","ncbi_id":"25870","summary":"The catalytic sites of sulfatases are only active if they contain a unique amino acid, C-alpha-formylglycine (FGly). The FGly residue is posttranslationally generated from a cysteine by enzymes with FGly-generating activity. The gene described in this record is a member of the sulfatase-modifying factor family and encodes a protein with a DUF323 domain that localizes to the lumen of the endoplasmic reticulum. This protein has low levels of FGly-generating activity but can heterodimerize with another family member - a protein with high levels of FGly-generating activity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":56064002,"end":56080670,"strand":1,"description":"sulfatase modifying factor 2 [Source:HGNC Symbol;Acc:HGNC:20415]"}, {"versioned_ensembl_gene_id":"ENSG00000260850.1","gene_symbol":"AC087564.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51354456,"end":51356532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269742.1","gene_symbol":"BNIP3P29","gene_name":"BCL2 interacting protein 3 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:49709]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421700","summary":null,"start":22065828,"end":22066398,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:49709]"}, {"versioned_ensembl_gene_id":"ENSG00000091039.16","gene_symbol":"OSBPL8","gene_name":"oxysterol binding protein like 8 [Source:HGNC Symbol;Acc:HGNC:16396]","synonyms":"OSBP10,ORP8,MSTP120,MST120","biotype":"protein_coding","ncbi_id":"114882","summary":"This gene encodes a member of a family of proteins containing an N-terminal pleckstrin homology domain and a highly conserved C-terminal oxysterol-binding protein-like sterol-binding domain. It binds mutliple lipid-containing molecules, including phosphatidylserine, phosphatidylinositol 4-phosphate (PI4P) and oxysterol, and promotes their exchange between the endoplasmic reticulum and the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":76351797,"end":76559809,"strand":-1,"description":"oxysterol binding protein like 8 [Source:HGNC Symbol;Acc:HGNC:16396]"}, {"versioned_ensembl_gene_id":"ENSG00000163206.5","gene_symbol":"SMCP","gene_name":"sperm mitochondria associated cysteine rich protein [Source:HGNC Symbol;Acc:HGNC:6962]","synonyms":"MCSP","biotype":"protein_coding","ncbi_id":"4184","summary":"Sperm mitochondria differ in morphology and subcellular localization from those of somatic cells. They are elongated, flattened, and arranged circumferentially to form a helical coiled sheath in the midpiece of the sperm flagellum. The protein encoded by this gene localizes to the capsule associated with the mitochondrial outer membranes and is thought to function in the organization and stabilization of the helical structure of the sperm's mitochondrial sheath. [provided by RefSeq, Jul 2008]","start":152878317,"end":152885047,"strand":1,"description":"sperm mitochondria associated cysteine rich protein [Source:HGNC Symbol;Acc:HGNC:6962]"}, {"versioned_ensembl_gene_id":"ENSG00000223502.1","gene_symbol":"AL731537.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51062579,"end":51068553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115816.14","gene_symbol":"CEBPZ","gene_name":"CCAAT/enhancer binding protein zeta [Source:HGNC Symbol;Acc:HGNC:24218]","synonyms":"CTF2,CBF2","biotype":"protein_coding","ncbi_id":"10153","summary":"This gene belongs to the CBF/Mak21 family. The encoded protein plays a role in cellular response to environmental stimuli through a transcriptional process that involves heat shock factors, conserved DNA elements (heat shock elements or HSEs) and CCAAT boxes. The protein acts as a DNA-binding transcriptional activator and regulates the heat-shock protein 70 (HSP70) promoter in a CCAAT-dependent manner. The protein is also involved in cell growth and differentiation, particularly, hematopoietic differentiation. [provided by RefSeq, Nov 2020]","start":37201612,"end":37231713,"strand":-1,"description":"CCAAT/enhancer binding protein zeta [Source:HGNC Symbol;Acc:HGNC:24218]"}, {"versioned_ensembl_gene_id":"ENSG00000197134.11","gene_symbol":"ZNF257","gene_name":"zinc finger protein 257 [Source:HGNC Symbol;Acc:HGNC:13498]","synonyms":"BMZF-4","biotype":"protein_coding","ncbi_id":"113835","summary":null,"start":22052452,"end":22091480,"strand":1,"description":"zinc finger protein 257 [Source:HGNC Symbol;Acc:HGNC:13498]"}, {"versioned_ensembl_gene_id":"ENSG00000113838.12","gene_symbol":"TBCCD1","gene_name":"TBCC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25546]","synonyms":"FLJ10560","biotype":"protein_coding","ncbi_id":"55171","summary":null,"start":186546073,"end":186570543,"strand":-1,"description":"TBCC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25546]"}, {"versioned_ensembl_gene_id":"ENSG00000236085.1","gene_symbol":"ACTG1P4","gene_name":"actin gamma 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:149]","synonyms":"ACTGP4","biotype":"processed_pseudogene","ncbi_id":"648740","summary":null,"start":103569553,"end":103570674,"strand":1,"description":"actin gamma 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:149]"}, {"versioned_ensembl_gene_id":"ENSG00000135473.14","gene_symbol":"PAN2","gene_name":"PAN2 poly(A) specific ribonuclease subunit [Source:HGNC Symbol;Acc:HGNC:20074]","synonyms":"USP52,KIAA0710,hPAN2","biotype":"protein_coding","ncbi_id":"9924","summary":"This gene encodes a deadenylase that functions as the catalytic subunit of the polyadenylate binding protein dependent poly(A) nuclease complex. The encoded protein is a magnesium dependent 3' to 5' exoribonuclease that is involved in the degradation of cytoplasmic mRNAs. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":56316223,"end":56334053,"strand":-1,"description":"PAN2 poly(A) specific ribonuclease subunit [Source:HGNC Symbol;Acc:HGNC:20074]"}, {"versioned_ensembl_gene_id":"ENSG00000170266.15","gene_symbol":"GLB1","gene_name":"galactosidase beta 1 [Source:HGNC Symbol;Acc:HGNC:4298]","synonyms":"ELNR1,EBP","biotype":"protein_coding","ncbi_id":"2720","summary":"This gene encodes a member of the glycosyl hydrolase 35 family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature lysosomal enzyme. This enzyme catalyzes the hydrolysis of a terminal beta-linked galactose residue from ganglioside substrates and other glycoconjugates. Mutations in this gene may result in GM1-gangliosidosis and Morquio B syndrome. [provided by RefSeq, Nov 2015]","start":32996608,"end":33097230,"strand":-1,"description":"galactosidase beta 1 [Source:HGNC Symbol;Acc:HGNC:4298]"}, {"versioned_ensembl_gene_id":"ENSG00000226215.6","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31728695,"end":31734489,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000223899.1","gene_symbol":"SEC13P1","gene_name":"SEC13 homolog, nuclear pore and COPII coat complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44529]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131671","summary":null,"start":33033863,"end":33034810,"strand":1,"description":"SEC13 homolog, nuclear pore and COPII coat complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44529]"}, {"versioned_ensembl_gene_id":"ENSG00000227527.2","gene_symbol":"AC096540.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":42335386,"end":42338376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198815.8","gene_symbol":"FOXJ3","gene_name":"forkhead box J3 [Source:HGNC Symbol;Acc:HGNC:29178]","synonyms":"KIAA1041","biotype":"protein_coding","ncbi_id":"22887","summary":null,"start":42176539,"end":42335877,"strand":-1,"description":"forkhead box J3 [Source:HGNC Symbol;Acc:HGNC:29178]"}, {"versioned_ensembl_gene_id":"ENSG00000140632.16","gene_symbol":"GLYR1","gene_name":"glyoxylate reductase 1 homolog [Source:HGNC Symbol;Acc:HGNC:24434]","synonyms":"NP60,N-PAC,HIBDL,BM045","biotype":"protein_coding","ncbi_id":"84656","summary":null,"start":4803203,"end":4847342,"strand":-1,"description":"glyoxylate reductase 1 homolog [Source:HGNC Symbol;Acc:HGNC:24434]"}, {"versioned_ensembl_gene_id":"ENSG00000123545.5","gene_symbol":"NDUFAF4","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:21034]","synonyms":"My013,HSPC125,HRPAP20,C6orf66,bA22L21.1","biotype":"protein_coding","ncbi_id":"29078","summary":"NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene are a cause of mitochondrial complex I deficiency. [provided by RefSeq, Oct 2009]","start":96889313,"end":96897881,"strand":-1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 [Source:HGNC Symbol;Acc:HGNC:21034]"}, {"versioned_ensembl_gene_id":"ENSG00000164776.9","gene_symbol":"PHKG1","gene_name":"phosphorylase kinase catalytic subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:8930]","synonyms":"PHKG","biotype":"protein_coding","ncbi_id":"5260","summary":"This gene is a member of the Ser/Thr protein kinase family and encodes a protein with one protein kinase domain and two calmodulin-binding domains. This protein is the catalytic member of a 16 subunit protein kinase complex which contains equimolar ratios of 4 subunit types. The complex is a crucial glycogenolytic regulatory enzyme. This gene has two pseudogenes at chromosome 7q11.21 and one at chromosome 11p11.12. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":56080283,"end":56092996,"strand":-1,"description":"phosphorylase kinase catalytic subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:8930]"}, {"versioned_ensembl_gene_id":"ENSG00000107798.17","gene_symbol":"LIPA","gene_name":"lipase A, lysosomal acid type [Source:HGNC Symbol;Acc:HGNC:6617]","synonyms":"LAL,CESD","biotype":"protein_coding","ncbi_id":"3988","summary":"This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014]","start":89213569,"end":89414557,"strand":-1,"description":"lipase A, lysosomal acid type [Source:HGNC Symbol;Acc:HGNC:6617]"}, {"versioned_ensembl_gene_id":"ENSG00000233159.1","gene_symbol":"AC007390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37194382,"end":37194737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244485.1","gene_symbol":"RPL18P13","gene_name":"ribosomal protein L18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35599]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441775","summary":null,"start":76235055,"end":76235623,"strand":-1,"description":"ribosomal protein L18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35599]"}, {"versioned_ensembl_gene_id":"ENSG00000260818.2","gene_symbol":"AC137527.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51277852,"end":51279112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260983.1","gene_symbol":"AC010528.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76228385,"end":76262365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204010.3","gene_symbol":"IFIT1B","gene_name":"interferon induced protein with tetratricopeptide repeats 1B [Source:HGNC Symbol;Acc:HGNC:23442]","synonyms":"IFIT1L,bA149I23.6","biotype":"protein_coding","ncbi_id":"439996","summary":null,"start":89378056,"end":89385205,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 1B [Source:HGNC Symbol;Acc:HGNC:23442]"}, {"versioned_ensembl_gene_id":"ENSG00000235897.1","gene_symbol":"TM4SF19-AS1","gene_name":"TM4SF19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41085]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874214","summary":null,"start":196318330,"end":196325570,"strand":1,"description":"TM4SF19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41085]"}, {"versioned_ensembl_gene_id":"ENSG00000228028.2","gene_symbol":"AC069257.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":196250542,"end":196251654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235942.2","gene_symbol":"LCE6A","gene_name":"late cornified envelope 6A [Source:HGNC Symbol;Acc:HGNC:31824]","synonyms":"C1orf44","biotype":"protein_coding","ncbi_id":"448835","summary":null,"start":152842868,"end":152843983,"strand":1,"description":"late cornified envelope 6A [Source:HGNC Symbol;Acc:HGNC:31824]"}, {"versioned_ensembl_gene_id":"ENSG00000257612.1","gene_symbol":"MIR4307HG","gene_name":"MIR4307 host gene [Source:HGNC Symbol;Acc:HGNC:52004]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927081","summary":null,"start":26873133,"end":26914743,"strand":1,"description":"MIR4307 host gene [Source:HGNC Symbol;Acc:HGNC:52004]"}, {"versioned_ensembl_gene_id":"ENSG00000226724.1","gene_symbol":"AC109780.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":186698520,"end":186708574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273331.1","gene_symbol":"TM4SF19-TCTEX1D2","gene_name":"TM4SF19-TCTEX1D2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49190]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534611","summary":"This locus represents naturally occurring read-through transcription between the neighboring transmembrane 4 L six family member 19 (TM4SF19) and Tctex1 domain containing 2 (TCTEX1D2) genes on chromosome 3. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus not expected to produce a protein product. [provided by RefSeq, Mar 2011]","start":196316082,"end":196338373,"strand":-1,"description":"TM4SF19-TCTEX1D2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49190]"}, {"versioned_ensembl_gene_id":"ENSG00000259218.5","gene_symbol":"LINC00928","gene_name":"long intergenic non-protein coding RNA 928 [Source:HGNC Symbol;Acc:HGNC:27535]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283761","summary":null,"start":89505277,"end":89524034,"strand":-1,"description":"long intergenic non-protein coding RNA 928 [Source:HGNC Symbol;Acc:HGNC:27535]"}, {"versioned_ensembl_gene_id":"ENSG00000258081.3","gene_symbol":"AL110292.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26836728,"end":27160420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269199.1","gene_symbol":"AC003973.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22043500,"end":22050005,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260194.1","gene_symbol":"AC007496.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53998313,"end":53999969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280392.1","gene_symbol":"AC007496.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53991012,"end":53994454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256155.1","gene_symbol":"AC022075.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10358464,"end":10361045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256288.1","gene_symbol":"AC022075.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10332861,"end":10338292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278562.3","gene_symbol":"AC243922.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70543654,"end":70549533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214074.3","gene_symbol":"RPL23AP39","gene_name":"ribosomal protein L23a pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36470]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271461","summary":null,"start":1730070,"end":1730474,"strand":1,"description":"ribosomal protein L23a pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36470]"}, {"versioned_ensembl_gene_id":"ENSG00000261047.1","gene_symbol":"AC137527.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51244054,"end":51244123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157890.17","gene_symbol":"MEGF11","gene_name":"multiple EGF like domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]","synonyms":"KIAA1781,DKFZp434L121","biotype":"protein_coding","ncbi_id":"84465","summary":null,"start":65895079,"end":66253747,"strand":-1,"description":"multiple EGF like domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]"}, {"versioned_ensembl_gene_id":"ENSG00000088812.17","gene_symbol":"ATRN","gene_name":"attractin [Source:HGNC Symbol;Acc:HGNC:885]","synonyms":"MGCA,DPPT-L","biotype":"protein_coding","ncbi_id":"8455","summary":"This gene encodes both membrane-bound and secreted protein isoforms. A membrane-bound isoform exhibits sequence similarity with the mouse mahogany protein, a receptor involved in controlling obesity. A secreted isoform is involved in the initial immune cell clustering during inflammatory responses that may regulate the chemotactic activity of chemokines. [provided by RefSeq, Apr 2016]","start":3471040,"end":3651122,"strand":1,"description":"attractin [Source:HGNC Symbol;Acc:HGNC:885]"}, {"versioned_ensembl_gene_id":"ENSG00000111832.12","gene_symbol":"RWDD1","gene_name":"RWD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20993]","synonyms":"PTD013","biotype":"protein_coding","ncbi_id":"51389","summary":null,"start":116571367,"end":116597675,"strand":1,"description":"RWD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20993]"}, {"versioned_ensembl_gene_id":"ENSG00000006118.14","gene_symbol":"TMEM132A","gene_name":"transmembrane protein 132A [Source:HGNC Symbol;Acc:HGNC:31092]","synonyms":"HSPA5BP1,GBP,FLJ20539","biotype":"protein_coding","ncbi_id":"54972","summary":"This gene encodes a protein that is highly similar to the rat Grp78-binding protein (GBP). Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":60924463,"end":60937159,"strand":1,"description":"transmembrane protein 132A [Source:HGNC Symbol;Acc:HGNC:31092]"}, {"versioned_ensembl_gene_id":"ENSG00000234431.2","gene_symbol":"AC007283.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":201166965,"end":201167546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281630.2","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195720361,"end":195740062,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000228794.8","gene_symbol":"LINC01128","gene_name":"long intergenic non-protein coding RNA 1128 [Source:HGNC Symbol;Acc:HGNC:49377]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"643837","summary":null,"start":825138,"end":859446,"strand":1,"description":"long intergenic non-protein coding RNA 1128 [Source:HGNC Symbol;Acc:HGNC:49377]"}, {"versioned_ensembl_gene_id":"ENSG00000179059.9","gene_symbol":"ZFP42","gene_name":"ZFP42 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:30949]","synonyms":"ZNF754,REX1","biotype":"protein_coding","ncbi_id":"132625","summary":null,"start":187995771,"end":188005050,"strand":1,"description":"ZFP42 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:30949]"}, {"versioned_ensembl_gene_id":"ENSG00000213123.10","gene_symbol":"TCTEX1D2","gene_name":"Tctex1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28482]","synonyms":"MGC33212","biotype":"protein_coding","ncbi_id":"255758","summary":"Dyneins are a group of microtubule-activated ATPases that function as molecular motors. They are divided into two subgroups of axonemal and cytoplasmic dyneins. The cytoplasmic dyneins function in intracellular motility, including retrograde axonal transport, protein sorting, organelle movement, and spindle dynamics. Molecules of conventional cytoplasmic dynein are comprised of 2 heavy chain polypeptides and a number of intermediate and light chains. This gene encodes a subunit of the human cytoplasmic dynein-2 complex. Mutations in this gene are associated with short-rib thoracic dysplasia 17 with or without polydactyly. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2017]","start":196291219,"end":196318299,"strand":-1,"description":"Tctex1 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28482]"}, {"versioned_ensembl_gene_id":"ENSG00000241003.1","gene_symbol":"AC108860.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94688228,"end":94688610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277185.1","gene_symbol":"GU182351.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54799454,"end":54811769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179148.9","gene_symbol":"ALOXE3","gene_name":"arachidonate lipoxygenase 3 [Source:HGNC Symbol;Acc:HGNC:13743]","synonyms":"eLOX3,E-LOX","biotype":"protein_coding","ncbi_id":"59344","summary":"This gene is a member of the lipoxygenase family, which are catabolized by arachidonic acid-derived compounds. The encoded enzyme is a hydroperoxide isomerase that synthesizes a unique type of epoxy alcohol (8R-hydroxy-11R,12R-epoxyeicosa-5Z,9E,14Z-trienoic acid) from 12R-hydroperoxyeicosatetraenoic acid (12R-HPETE). This epoxy alcohol can activate the the nuclear receptor peroxisome proliferator-activated receptor alpha (PPARalpha), which is implicated in epidermal differentiation. Loss of function of the enzyme encoded by this gene results in ichthyosis, implicating the function of this gene in the differentiation of human skin. This gene is part of a cluster of lipoxygenase genes on 17p13.1. Mutations in this gene result in nonbullous congenital ichthyosiform erythroderma (NCIE). Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":8095900,"end":8119047,"strand":-1,"description":"arachidonate lipoxygenase 3 [Source:HGNC Symbol;Acc:HGNC:13743]"}, {"versioned_ensembl_gene_id":"ENSG00000215146.4","gene_symbol":"BX322639.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42331866,"end":42367974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206144.5","gene_symbol":"AC022034.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53537060,"end":53540300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278207.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"47.11,p58.1,nkat1,cl-42,CD158A","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814235,"end":54828734,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000277236.4","gene_symbol":"CCL14","gene_name":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]","synonyms":"MCIF,HCC-3,HCC-1,CKb1,SCYL2,SCYA14,NCC-2","biotype":"protein_coding","ncbi_id":"6358","summary":"This gene, chemokine (C-C motif) ligand 14, is one of several CC cytokine genes clustered on 17q11.2. The CC cytokines are secreted proteins characterized by two adjacent cysteines. The cytokine encoded by this gene induces changes in intracellular calcium concentration and enzyme release in monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Read-through transcripts are also expressed that include exons from the upstream cytokine gene, chemokine (C-C motif) ligand 15, and are represented as GeneID: 348249. [provided by RefSeq, Dec 2009]","start":35983323,"end":35987036,"strand":-1,"description":"C-C motif chemokine ligand 14 [Source:HGNC Symbol;Acc:HGNC:10612]"}, {"versioned_ensembl_gene_id":"ENSG00000100342.20","gene_symbol":"APOL1","gene_name":"apolipoprotein L1 [Source:HGNC Symbol;Acc:HGNC:618]","synonyms":"APOL","biotype":"protein_coding","ncbi_id":"8542","summary":"This gene encodes a secreted high density lipoprotein which binds to apolipoprotein A-I. Apolipoprotein A-I is a relatively abundant plasma protein and is the major apoprotein of HDL. It is involved in the formation of most cholesteryl esters in plasma and also promotes efflux of cholesterol from cells. This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Several different transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":36253010,"end":36267530,"strand":1,"description":"apolipoprotein L1 [Source:HGNC Symbol;Acc:HGNC:618]"}, {"versioned_ensembl_gene_id":"ENSG00000215834.10","gene_symbol":"FMO9P","gene_name":"flavin containing monooxygenase 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:32210]","synonyms":"RP11-45J16.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"116123","summary":null,"start":166603916,"end":166631400,"strand":1,"description":"flavin containing monooxygenase 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:32210]"}, {"versioned_ensembl_gene_id":"ENSG00000176428.5","gene_symbol":"VPS37D","gene_name":"VPS37D, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:18287]","synonyms":"WBSCR24,MGC35352","biotype":"protein_coding","ncbi_id":"155382","summary":null,"start":73667825,"end":73672112,"strand":1,"description":"VPS37D, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:18287]"}, {"versioned_ensembl_gene_id":"ENSG00000231831.1","gene_symbol":"MTHFD1P1","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7433]","synonyms":"MTHFDP1,MTHFDL1","biotype":"processed_pseudogene","ncbi_id":"4523","summary":null,"start":57392646,"end":57395409,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7433]"}, {"versioned_ensembl_gene_id":"ENSG00000234143.1","gene_symbol":"UGT1A13P","gene_name":"UDP glucuronosyltransferase family 1 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32191]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"404204","summary":null,"start":233647926,"end":233649026,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A13, pseudogene [Source:HGNC Symbol;Acc:HGNC:32191]"}, {"versioned_ensembl_gene_id":"ENSG00000242958.1","gene_symbol":"AC040975.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28810103,"end":28810418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236772.1","gene_symbol":"AL034550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32449755,"end":32453607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277301.1","gene_symbol":"AL034550.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32509959,"end":32520285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177994.15","gene_symbol":"C2orf73","gene_name":"chromosome 2 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:26861]","synonyms":"FLJ40298","biotype":"protein_coding","ncbi_id":"129852","summary":null,"start":54330034,"end":54383742,"strand":1,"description":"chromosome 2 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:26861]"}, {"versioned_ensembl_gene_id":"ENSG00000279011.1","gene_symbol":"AC091905.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10057502,"end":10057807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279755.1","gene_symbol":"AC091905.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10064243,"end":10064476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225429.1","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33105723,"end":33106989,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000253586.1","gene_symbol":"AC067817.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38799643,"end":38802296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281553.2","gene_symbol":"AC131097.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":241893989,"end":241902551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242366.3","gene_symbol":"UGT1A8","gene_name":"UDP glucuronosyltransferase family 1 member A8 [Source:HGNC Symbol;Acc:HGNC:12540]","synonyms":"UGT1H","biotype":"protein_coding","ncbi_id":"54576","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity with many substrates including coumarins, phenols, anthraquinones, flavones, and some opioids. [provided by RefSeq, Jul 2008]","start":233617645,"end":233773310,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A8 [Source:HGNC Symbol;Acc:HGNC:12540]"}, {"versioned_ensembl_gene_id":"ENSG00000165591.6","gene_symbol":"FAAH2","gene_name":"fatty acid amide hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:26440]","synonyms":"RP11-479E16.1,FLJ31204,FAAH-2,AMDD","biotype":"protein_coding","ncbi_id":"158584","summary":"This gene encodes a fatty acid amide hydrolase that shares a conserved protein motif with the amidase signature family of enzymes. The encoded enzyme is able to catalyze the hydrolysis of a broad range of bioactive lipids, including those from the three main classes of fatty acid amides; N-acylethanolamines, fatty acid primary amides and N-acyl amino acids. This enzyme has a preference for monounsaturated acyl chains as a substrate. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]","start":57286706,"end":57489196,"strand":1,"description":"fatty acid amide hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:26440]"}, {"versioned_ensembl_gene_id":"ENSG00000204393.7","gene_symbol":"AL133343.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32564992,"end":32608893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223687.4","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28991375,"end":29001915,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000259224.2","gene_symbol":"SLC35G6","gene_name":"solute carrier family 35 member G6 [Source:HGNC Symbol;Acc:HGNC:31351]","synonyms":"TMEM21B,AMAC1L3","biotype":"protein_coding","ncbi_id":"643664","summary":null,"start":7481332,"end":7483496,"strand":1,"description":"solute carrier family 35 member G6 [Source:HGNC Symbol;Acc:HGNC:31351]"}, {"versioned_ensembl_gene_id":"ENSG00000037637.10","gene_symbol":"FBXO42","gene_name":"F-box protein 42 [Source:HGNC Symbol;Acc:HGNC:29249]","synonyms":"KIAA1332,Fbx42","biotype":"protein_coding","ncbi_id":"54455","summary":"Members of the F-box protein family, such as FBXO42, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (SKP1A; MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Dec 2010]","start":16246839,"end":16352454,"strand":-1,"description":"F-box protein 42 [Source:HGNC Symbol;Acc:HGNC:29249]"}, {"versioned_ensembl_gene_id":"ENSG00000275848.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54848033,"end":54858928,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000233293.1","gene_symbol":"AL133343.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32561093,"end":32573888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174282.11","gene_symbol":"ZBTB4","gene_name":"zinc finger and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23847]","synonyms":"KIAA1538,KAISO-L1,ZNF903","biotype":"protein_coding","ncbi_id":"57659","summary":null,"start":7459366,"end":7484263,"strand":-1,"description":"zinc finger and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23847]"}, {"versioned_ensembl_gene_id":"ENSG00000262795.5","gene_symbol":"IFNGR2","gene_name":"interferon gamma receptor 2 [Source:HGNC Symbol;Acc:HGNC:5440]","synonyms":"IFNGT1,AF-1","biotype":"protein_coding","ncbi_id":"3460","summary":"This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008]","start":33410836,"end":33488905,"strand":1,"description":"interferon gamma receptor 2 [Source:HGNC Symbol;Acc:HGNC:5440]"}, {"versioned_ensembl_gene_id":"ENSG00000282250.1","gene_symbol":"AC245594.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":39314619,"end":39346102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117154.11","gene_symbol":"IGSF21","gene_name":"immunoglobin superfamily member 21 [Source:HGNC Symbol;Acc:HGNC:28246]","synonyms":"RP11-121A23.1,MGC15730","biotype":"protein_coding","ncbi_id":"84966","summary":"This gene encodes a protein which has two immunoglobulin (Ig) domains and is a member of the immunoglobulin superfamily. Proteins in this superfamily are usually found on or in cell membranes and act as receptors in immune response pathways. [provided by RefSeq, Sep 2011]","start":18107746,"end":18378483,"strand":1,"description":"immunoglobin superfamily member 21 [Source:HGNC Symbol;Acc:HGNC:28246]"}, {"versioned_ensembl_gene_id":"ENSG00000276781.3","gene_symbol":"CHGA","gene_name":"chromogranin A [Source:HGNC Symbol;Acc:HGNC:1929]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1113","summary":"The protein encoded by this gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. It is found in secretory vesicles of neurons and endocrine cells. This gene product is a precursor to three biologically active peptides; vasostatin, pancreastatin, and parastatin. These peptides act as autocrine or paracrine negative modulators of the neuroendocrine system. Two other peptides, catestatin and chromofungin, have antimicrobial activity and antifungal activity, respectively. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":92923080,"end":92935293,"strand":1,"description":"chromogranin A [Source:HGNC Symbol;Acc:HGNC:1929]"}, {"versioned_ensembl_gene_id":"ENSG00000205861.11","gene_symbol":"PCOTH","gene_name":"Pro-X-Gly collagen triple helix like repeat containing [Source:HGNC Symbol;Acc:HGNC:39839]","synonyms":"C1QTNF9B-AS1","biotype":"protein_coding","ncbi_id":"542767","summary":null,"start":23888889,"end":23897263,"strand":1,"description":"Pro-X-Gly collagen triple helix like repeat containing [Source:HGNC Symbol;Acc:HGNC:39839]"}, {"versioned_ensembl_gene_id":"ENSG00000205670.10","gene_symbol":"SMIM11A","gene_name":"small integral membrane protein 11A [Source:HGNC Symbol;Acc:HGNC:1293]","synonyms":"SMIM11,FAM165B,C21orf51","biotype":"protein_coding","ncbi_id":"54065","summary":null,"start":34375480,"end":34407866,"strand":1,"description":"small integral membrane protein 11A [Source:HGNC Symbol;Acc:HGNC:1293]"}, {"versioned_ensembl_gene_id":"ENSG00000027001.9","gene_symbol":"MIPEP","gene_name":"mitochondrial intermediate peptidase [Source:HGNC Symbol;Acc:HGNC:7104]","synonyms":"MIP","biotype":"protein_coding","ncbi_id":"4285","summary":"The product of this gene performs the final step in processing a specific class of nuclear-encoded proteins targeted to the mitochondrial matrix or inner membrane. This protein is primarily involved in the maturation of oxidative phosphorylation (OXPHOS)-related proteins. This gene may contribute to the functional effects of frataxin deficiency and the clinical manifestations of Friedreich ataxia. [provided by RefSeq, Jul 2008]","start":23730189,"end":23889419,"strand":-1,"description":"mitochondrial intermediate peptidase [Source:HGNC Symbol;Acc:HGNC:7104]"}, {"versioned_ensembl_gene_id":"ENSG00000278874.1","gene_symbol":"AC091905.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10070531,"end":10070841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280016.1","gene_symbol":"AC091905.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10082571,"end":10082772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082146.12","gene_symbol":"STRADB","gene_name":"STE20-related kinase adaptor beta [Source:HGNC Symbol;Acc:HGNC:13205]","synonyms":"PAPK,ILPIPA,ILPIP,CALS-21,ALS2CR2","biotype":"protein_coding","ncbi_id":"55437","summary":"This gene encodes a protein that belongs to the serine/threonine protein kinase STE20 subfamily. One of the active site residues in the protein kinase domain of this protein is altered, and it is thus a pseudokinase. This protein is a component of a complex involved in the activation of serine/threonine kinase 11, a master kinase that regulates cell polarity and energy-generating metabolism. This complex regulates the relocation of this kinase from the nucleus to the cytoplasm, and it is essential for G1 cell cycle arrest mediated by this kinase. The protein encoded by this gene can also interact with the X chromosome-linked inhibitor of apoptosis protein, and this interaction enhances the anti-apoptotic activity of this protein via the JNK1 signal transduction pathway. Two pseudogenes, located on chromosomes 1 and 7, have been found for this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":201387858,"end":201480846,"strand":1,"description":"STE20-related kinase adaptor beta [Source:HGNC Symbol;Acc:HGNC:13205]"}, {"versioned_ensembl_gene_id":"ENSG00000105519.15","gene_symbol":"CAPS","gene_name":"calcyphosine [Source:HGNC Symbol;Acc:HGNC:1487]","synonyms":"MGC126562,CAPS1","biotype":"protein_coding","ncbi_id":"828","summary":"This gene encodes a calcium-binding protein, which may play a role in the regulation of ion transport. A similar protein was first described as a potentially important regulatory protein in the dog thyroid and was termed as R2D5 antigen in rabbit. Alternative splicing of this gene generates two transcript variants. [provided by RefSeq, Jul 2008]","start":5911707,"end":5915877,"strand":1,"description":"calcyphosine [Source:HGNC Symbol;Acc:HGNC:1487]"}, {"versioned_ensembl_gene_id":"ENSG00000234984.1","gene_symbol":"FMO10P","gene_name":"flavin containing monooxygenase 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:32211]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128181","summary":null,"start":166665885,"end":166682196,"strand":1,"description":"flavin containing monooxygenase 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:32211]"}, {"versioned_ensembl_gene_id":"ENSG00000228445.1","gene_symbol":"UGT1A2P","gene_name":"UDP glucuronosyltransferase family 1 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12534]","synonyms":"UGT1BP","biotype":"unprocessed_pseudogene","ncbi_id":"54580","summary":null,"start":233747214,"end":233748079,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:12534]"}, {"versioned_ensembl_gene_id":"ENSG00000230035.2","gene_symbol":"AL359738.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18166929,"end":18179346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243135.6","gene_symbol":"UGT1A3","gene_name":"UDP glucuronosyltransferase family 1 member A3 [Source:HGNC Symbol;Acc:HGNC:12535]","synonyms":"UGT1C","biotype":"protein_coding","ncbi_id":"54659","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. Substrates of this enzyme include estrone, 2-hydroxyestrone, and metabolites of benzo alpha-pyrene. [provided by RefSeq, Jul 2008]","start":233729108,"end":233773299,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A3 [Source:HGNC Symbol;Acc:HGNC:12535]"}, {"versioned_ensembl_gene_id":"ENSG00000263072.6","gene_symbol":"ZNF213-AS1","gene_name":"ZNF213 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50505]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507458","summary":null,"start":3110460,"end":3134882,"strand":-1,"description":"ZNF213 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50505]"}, {"versioned_ensembl_gene_id":"ENSG00000280222.1","gene_symbol":"AL365209.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18109389,"end":18115861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258172.1","gene_symbol":"AC073655.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94272150,"end":94277195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257052.1","gene_symbol":"AP003721.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60906789,"end":60909742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227802.1","gene_symbol":"DNAJB3","gene_name":"DnaJ heat shock protein family (Hsp40) member B3 [Source:HGNC Symbol;Acc:HGNC:32397]","synonyms":"HCG3","biotype":"transcribed_processed_pseudogene","ncbi_id":"414061","summary":null,"start":233742750,"end":233744015,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B3 [Source:HGNC Symbol;Acc:HGNC:32397]"}, {"versioned_ensembl_gene_id":"ENSG00000213250.5","gene_symbol":"RBMS2P1","gene_name":"RNA binding motif single stranded interacting protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30994]","synonyms":"RBMS2P","biotype":"processed_pseudogene","ncbi_id":"643427","summary":null,"start":94423744,"end":94424969,"strand":-1,"description":"RNA binding motif single stranded interacting protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30994]"}, {"versioned_ensembl_gene_id":"ENSG00000250620.1","gene_symbol":"LINC02515","gene_name":"long intergenic non-protein coding RNA 2515 [Source:HGNC Symbol;Acc:HGNC:53504]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723920","summary":null,"start":187413564,"end":187415697,"strand":1,"description":"long intergenic non-protein coding RNA 2515 [Source:HGNC Symbol;Acc:HGNC:53504]"}, {"versioned_ensembl_gene_id":"ENSG00000258365.1","gene_symbol":"AC073655.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94277758,"end":94282844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251643.1","gene_symbol":"AC093763.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187441677,"end":187444298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251490.1","gene_symbol":"AC093763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187516153,"end":187517208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125354.22","gene_symbol":"SEPT6","gene_name":"septin 6 [Source:HGNC Symbol;Acc:HGNC:15848]","synonyms":"SEPT2,SEP2,MGC20339,MGC16619,KIAA0128","biotype":"protein_coding","ncbi_id":"23157","summary":"This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":119615724,"end":119693370,"strand":-1,"description":"septin 6 [Source:HGNC Symbol;Acc:HGNC:15848]"}, {"versioned_ensembl_gene_id":"ENSG00000234548.5","gene_symbol":"LINC02020","gene_name":"long intergenic non-protein coding RNA 2020 [Source:HGNC Symbol;Acc:HGNC:52855]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986164","summary":null,"start":186440345,"end":186450696,"strand":1,"description":"long intergenic non-protein coding RNA 2020 [Source:HGNC Symbol;Acc:HGNC:52855]"}, {"versioned_ensembl_gene_id":"ENSG00000137274.12","gene_symbol":"BPHL","gene_name":"biphenyl hydrolase like [Source:HGNC Symbol;Acc:HGNC:1094]","synonyms":"VACVase,MCNAA,Bph-rp","biotype":"protein_coding","ncbi_id":"670","summary":"This gene encodes a member of the serine protease family of hydrolytic enzymes which contain a serine in their active site. The encoded protein may play a role in activation of the antiviral prodrug valacyclovir. Alternatively spliced transcript variants have been described.[provided by RefSeq, Jan 2009]","start":3118374,"end":3153578,"strand":1,"description":"biphenyl hydrolase like [Source:HGNC Symbol;Acc:HGNC:1094]"}, {"versioned_ensembl_gene_id":"ENSG00000250859.1","gene_symbol":"HNRNPKP1","gene_name":"heterogeneous nuclear ribonucleoprotein K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389322","summary":null,"start":127511464,"end":127512842,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42374]"}, {"versioned_ensembl_gene_id":"ENSG00000261534.1","gene_symbol":"AL596244.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":121815674,"end":121819452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242515.5","gene_symbol":"UGT1A10","gene_name":"UDP glucuronosyltransferase family 1 member A10 [Source:HGNC Symbol;Acc:HGNC:12531]","synonyms":"UGT1J","biotype":"protein_coding","ncbi_id":"54575","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity on mycophenolic acid, coumarins, and quinolines. [provided by RefSeq, Jul 2008]","start":233636454,"end":233773305,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A10 [Source:HGNC Symbol;Acc:HGNC:12531]"}, {"versioned_ensembl_gene_id":"ENSG00000071462.11","gene_symbol":"BUD23","gene_name":"BUD23, rRNA methyltransferase and ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:16405]","synonyms":"WBSCR22,WBMT,PP3381,MGC5140,MGC2022,MGC19709,MERM1","biotype":"protein_coding","ncbi_id":"114049","summary":"This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]","start":73683025,"end":73705161,"strand":1,"description":"BUD23, rRNA methyltransferase and ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:16405]"}, {"versioned_ensembl_gene_id":"ENSG00000136040.8","gene_symbol":"PLXNC1","gene_name":"plexin C1 [Source:HGNC Symbol;Acc:HGNC:9106]","synonyms":"VESPR,CD232","biotype":"protein_coding","ncbi_id":"10154","summary":"This gene encodes a member of the plexin family. Plexins are transmembrane receptors for semaphorins, a large family of proteins that regulate axon guidance, cell motility and migration, and the immune response. The encoded protein and its ligand regulate melanocyte adhesion, and viral semaphorins may modulate the immune response by binding to this receptor. The encoded protein may be a tumor suppressor protein for melanoma. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2011]","start":94148723,"end":94307675,"strand":1,"description":"plexin C1 [Source:HGNC Symbol;Acc:HGNC:9106]"}, {"versioned_ensembl_gene_id":"ENSG00000272092.1","gene_symbol":"AC087623.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38382364,"end":38383461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222018.1","gene_symbol":"C21orf140","gene_name":"chromosome 21 open reading frame 140 [Source:HGNC Symbol;Acc:HGNC:39602]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928147","summary":null,"start":34400317,"end":34401072,"strand":-1,"description":"chromosome 21 open reading frame 140 [Source:HGNC Symbol;Acc:HGNC:39602]"}, {"versioned_ensembl_gene_id":"ENSG00000254898.1","gene_symbol":"AC087362.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38335981,"end":38337551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185404.16","gene_symbol":"SP140L","gene_name":"SP140 nuclear body protein like [Source:HGNC Symbol;Acc:HGNC:25105]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93349","summary":null,"start":230327184,"end":230403732,"strand":1,"description":"SP140 nuclear body protein like [Source:HGNC Symbol;Acc:HGNC:25105]"}, {"versioned_ensembl_gene_id":"ENSG00000255487.1","gene_symbol":"AC087362.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38275888,"end":38276680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249642.1","gene_symbol":"AC097521.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187613765,"end":187660369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139372.14","gene_symbol":"TDG","gene_name":"thymine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:11700]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6996","summary":"The protein encoded by this gene belongs to the TDG/mug DNA glycosylase family. Thymine-DNA glycosylase (TDG) removes thymine moieties from G/T mismatches by hydrolyzing the carbon-nitrogen bond between the sugar-phosphate backbone of DNA and the mispaired thymine. With lower activity, this enzyme also removes thymine from C/T and T/T mispairings. TDG can also remove uracil and 5-bromouracil from mispairings with guanine. This enzyme plays a central role in cellular defense against genetic mutation caused by the spontaneous deamination of 5-methylcytosine and cytosine. This gene may have a pseudogene in the p arm of chromosome 12. [provided by RefSeq, Jul 2008]","start":103965804,"end":103988874,"strand":1,"description":"thymine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:11700]"}, {"versioned_ensembl_gene_id":"ENSG00000250590.5","gene_symbol":"LINC02492","gene_name":"long intergenic non-protein coding RNA 2492 [Source:HGNC Symbol;Acc:HGNC:53476]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506272","summary":null,"start":187532878,"end":187672641,"strand":-1,"description":"long intergenic non-protein coding RNA 2492 [Source:HGNC Symbol;Acc:HGNC:53476]"}, {"versioned_ensembl_gene_id":"ENSG00000276254.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8","biotype":"unprocessed_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877174,"end":54891588,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000085788.13","gene_symbol":"DDHD2","gene_name":"DDHD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29106]","synonyms":"SPG54,SAMWD1,KIAA0725","biotype":"protein_coding","ncbi_id":"23259","summary":"This gene encodes a phospholipase enzyme containing sterile-alpha-motif (SAM), WWE, and DDHD domains. This protein participates in membrane trafficking between the endoplastic reticulum and the Golgi body. Mutations in this gene can cause autosomal recessive spastic paraplegia 54. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":38225218,"end":38275558,"strand":1,"description":"DDHD domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29106]"}, {"versioned_ensembl_gene_id":"ENSG00000068400.13","gene_symbol":"GRIPAP1","gene_name":"GRIP1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18706]","synonyms":"MPMGp800B12492Q3,KIAA1167,GRASP1,GRASP-1,DKFZp434P0630","biotype":"protein_coding","ncbi_id":"56850","summary":"This gene encodes a guanine nucleotide exchange factor for the Ras family of small G proteins (RasGEF). The encoded protein interacts in a complex with glutamate receptor interacting protein 1 (GRIP1) and plays a role in the regulation of AMPA receptor function. [provided by RefSeq, Aug 2013]","start":48973720,"end":49002264,"strand":-1,"description":"GRIP1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18706]"}, {"versioned_ensembl_gene_id":"ENSG00000249577.1","gene_symbol":"AC010424.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127465822,"end":127466118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250030.2","gene_symbol":"AC104806.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67446267,"end":67446574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281305.1","gene_symbol":"LINC00574","gene_name":"long intergenic non-protein coding RNA 574 [Source:HGNC Symbol;Acc:HGNC:21598]","synonyms":"FLJ13162,dJ182D15.1,C6orf208","biotype":"lincRNA","ncbi_id":"80069","summary":null,"start":169790321,"end":169802873,"strand":1,"description":"long intergenic non-protein coding RNA 574 [Source:HGNC Symbol;Acc:HGNC:21598]"}, {"versioned_ensembl_gene_id":"ENSG00000225239.1","gene_symbol":"RPL21P107","gene_name":"ribosomal protein L21 pseudogene 107 [Source:HGNC Symbol;Acc:HGNC:36313]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644627","summary":null,"start":110762674,"end":110763133,"strand":-1,"description":"ribosomal protein L21 pseudogene 107 [Source:HGNC Symbol;Acc:HGNC:36313]"}, {"versioned_ensembl_gene_id":"ENSG00000274920.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54860886,"end":54875194,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000205863.10","gene_symbol":"C1QTNF9B","gene_name":"C1q and TNF related 9B [Source:HGNC Symbol;Acc:HGNC:34072]","synonyms":"CTRP9B","biotype":"protein_coding","ncbi_id":"387911","summary":null,"start":23890525,"end":23902655,"strand":-1,"description":"C1q and TNF related 9B [Source:HGNC Symbol;Acc:HGNC:34072]"}, {"versioned_ensembl_gene_id":"ENSG00000031823.14","gene_symbol":"RANBP3","gene_name":"RAN binding protein 3 [Source:HGNC Symbol;Acc:HGNC:9850]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8498","summary":"This gene encodes a protein with a RanBD1 domain that is found in both the nucleus and cytoplasm. This protein plays a role in nuclear export as part of a heteromeric complex. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":5916139,"end":5978142,"strand":-1,"description":"RAN binding protein 3 [Source:HGNC Symbol;Acc:HGNC:9850]"}, {"versioned_ensembl_gene_id":"ENSG00000231476.1","gene_symbol":"AC074389.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1620654,"end":1621405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221954.2","gene_symbol":"OR4C12","gene_name":"olfactory receptor family 4 subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:15168]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49981473,"end":49982535,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:15168]"}, {"versioned_ensembl_gene_id":"ENSG00000100410.7","gene_symbol":"PHF5A","gene_name":"PHD finger protein 5A [Source:HGNC Symbol;Acc:HGNC:18000]","synonyms":"SF3B7,SF3b14b,SAP14b,Rds3,MGC1346,INI,bK223H9.2","biotype":"protein_coding","ncbi_id":"84844","summary":"This gene encodes a subunit of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence-independent manner and may anchor the U2 snRNP to the pre-mRNA. The protein encoded by this gene contains a PHD-finger-like domain that is flanked by highly basic N- and C-termini. This protein belongs to the PHD-finger superfamily and may act as a chromatin-associated protein. This gene has several pseudogenes on different chromosomes. [provided by RefSeq, Jul 2008]","start":41459717,"end":41468725,"strand":-1,"description":"PHD finger protein 5A [Source:HGNC Symbol;Acc:HGNC:18000]"}, {"versioned_ensembl_gene_id":"ENSG00000254649.1","gene_symbol":"AP003086.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78388061,"end":78392405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276413.1","gene_symbol":"AL078604.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159555964,"end":159556174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225533.1","gene_symbol":"PAWRP1","gene_name":"pro-apoptotic WT1 regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45201]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420526","summary":null,"start":95183653,"end":95184217,"strand":1,"description":"pro-apoptotic WT1 regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45201]"}, {"versioned_ensembl_gene_id":"ENSG00000216480.2","gene_symbol":"AL078604.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159526062,"end":159526527,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227269.1","gene_symbol":"AL162427.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99183373,"end":99184891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229625.3","gene_symbol":"AC016877.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98961428,"end":98968284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155438.11","gene_symbol":"NIFK","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 [Source:HGNC Symbol;Acc:HGNC:17838]","synonyms":"Nopp34,MKI67IP,hNIFK","biotype":"protein_coding","ncbi_id":"84365","summary":"This gene encodes a protein that interacts with the forkhead-associated domain of the Ki-67 antigen. The encoded protein may bind RNA and may play a role in mitosis and cell cycle progression. Multiple pseudogenes exist on chromosomes 5, 10, 12, 15, and 19.[provided by RefSeq, Jan 2009]","start":121726945,"end":121736923,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 [Source:HGNC Symbol;Acc:HGNC:17838]"}, {"versioned_ensembl_gene_id":"ENSG00000224321.1","gene_symbol":"RPL12P14","gene_name":"ribosomal protein L12 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36495]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729500","summary":null,"start":15792796,"end":15793285,"strand":1,"description":"ribosomal protein L12 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36495]"}, {"versioned_ensembl_gene_id":"ENSG00000167487.11","gene_symbol":"KLHL26","gene_name":"kelch like family member 26 [Source:HGNC Symbol;Acc:HGNC:25623]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55295","summary":null,"start":18636965,"end":18671714,"strand":1,"description":"kelch like family member 26 [Source:HGNC Symbol;Acc:HGNC:25623]"}, {"versioned_ensembl_gene_id":"ENSG00000129451.11","gene_symbol":"KLK10","gene_name":"kallikrein related peptidase 10 [Source:HGNC Symbol;Acc:HGNC:6358]","synonyms":"PRSSL1,NES1","biotype":"protein_coding","ncbi_id":"5655","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its encoded protein is secreted and may play a role in suppression of tumorigenesis in breast and prostate cancers. Alternate splicing of this gene results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":51012739,"end":51020175,"strand":-1,"description":"kallikrein related peptidase 10 [Source:HGNC Symbol;Acc:HGNC:6358]"}, {"versioned_ensembl_gene_id":"ENSG00000228262.8","gene_symbol":"LINC01320","gene_name":"long intergenic non-protein coding RNA 1320 [Source:HGNC Symbol;Acc:HGNC:50526]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355288","summary":null,"start":34677555,"end":34738231,"strand":1,"description":"long intergenic non-protein coding RNA 1320 [Source:HGNC Symbol;Acc:HGNC:50526]"}, {"versioned_ensembl_gene_id":"ENSG00000281077.1","gene_symbol":"LINC02557","gene_name":"long intergenic non-protein coding RNA 2557 [Source:HGNC Symbol;Acc:HGNC:53596]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372955","summary":null,"start":23536736,"end":23537844,"strand":-1,"description":"long intergenic non-protein coding RNA 2557 [Source:HGNC Symbol;Acc:HGNC:53596]"}, {"versioned_ensembl_gene_id":"ENSG00000128694.11","gene_symbol":"OSGEPL1","gene_name":"O-sialoglycoprotein endopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:23075]","synonyms":"Qri7,OSGEPL","biotype":"protein_coding","ncbi_id":"64172","summary":null,"start":189746660,"end":189763227,"strand":-1,"description":"O-sialoglycoprotein endopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:23075]"}, {"versioned_ensembl_gene_id":"ENSG00000242925.1","gene_symbol":"PLCH1-AS2","gene_name":"PLCH1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41232]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874036","summary":null,"start":155485803,"end":155487121,"strand":1,"description":"PLCH1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41232]"}, {"versioned_ensembl_gene_id":"ENSG00000243518.1","gene_symbol":"AC108729.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155401329,"end":155403399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149196.15","gene_symbol":"HIKESHI","gene_name":"Hikeshi, heat shock protein nuclear import factor [Source:HGNC Symbol;Acc:HGNC:26938]","synonyms":"OPI10,HSPC179,HSPC138,C11orf73","biotype":"protein_coding","ncbi_id":"51501","summary":"This gene encodes an evolutionarily conserved nuclear transport receptor that mediates heat-shock-induced nuclear import of 70 kDa heat-shock proteins (Hsp70s) through interactions with FG-nucleoporins. The protein mediates transport of the ATP form but not the ADP form of Hsp70 proteins under conditions of heat shock stress. Structural analyses demonstrate that the protein forms an asymmetric homodimer and that the N-terminal domain consists of a jelly-roll/beta-sandwich fold structure that contains hydrophobic pockets involved in FG-nucleoporin recognition. Reduction of RNA expression levels in HeLa cells using small interfering RNAs results in inhibition of heat shock-induced nuclear accumulation of Hsp70s, indicating a role for this gene in regulation of Hsp70 nuclear import during heat shock stress. [provided by RefSeq, Apr 2016]","start":86302211,"end":86345931,"strand":1,"description":"Hikeshi, heat shock protein nuclear import factor [Source:HGNC Symbol;Acc:HGNC:26938]"}, {"versioned_ensembl_gene_id":"ENSG00000267083.1","gene_symbol":"KRT18P61","gene_name":"keratin 18 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:48888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418865","summary":null,"start":60810165,"end":60811462,"strand":1,"description":"keratin 18 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:48888]"}, {"versioned_ensembl_gene_id":"ENSG00000234249.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33137211,"end":33140747,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000254539.1","gene_symbol":"AC239804.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149048576,"end":149051273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226004.1","gene_symbol":"AL591468.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137943079,"end":137945802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229922.5","gene_symbol":"LINC02528","gene_name":"long intergenic non-protein coding RNA 2528 [Source:HGNC Symbol;Acc:HGNC:53554]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378020","summary":null,"start":137945366,"end":137972522,"strand":1,"description":"long intergenic non-protein coding RNA 2528 [Source:HGNC Symbol;Acc:HGNC:53554]"}, {"versioned_ensembl_gene_id":"ENSG00000164935.6","gene_symbol":"DCSTAMP","gene_name":"dendrocyte expressed seven transmembrane protein [Source:HGNC Symbol;Acc:HGNC:18549]","synonyms":"TM7SF4,FIND,DC-STAMP","biotype":"protein_coding","ncbi_id":"81501","summary":"This gene encodes a seven-pass transmembrane protein that is primarily expressed in dendritic cells. The encoded protein is involved in a range of immunological functions carried out by dendritic cells. This protein plays a role in osteoclastogenesis and myeloid differentiation. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":104339087,"end":104356689,"strand":1,"description":"dendrocyte expressed seven transmembrane protein [Source:HGNC Symbol;Acc:HGNC:18549]"}, {"versioned_ensembl_gene_id":"ENSG00000007047.14","gene_symbol":"MARK4","gene_name":"microtubule affinity regulating kinase 4 [Source:HGNC Symbol;Acc:HGNC:13538]","synonyms":"PAR-1D,Nbla00650,MARKL1,KIAA1860,FLJ90097","biotype":"protein_coding","ncbi_id":"57787","summary":"This gene encodes a member of the microtubule affinity-regulating kinase family. These protein kinases phosphorylate microtubule-associated proteins and regulate the transition between stable and dynamic microtubules. The encoded protein is associated with the centrosome throughout mitosis and may be involved in cell cycle control. Expression of this gene is a potential marker for cancer, and the encoded protein may also play a role in Alzheimer's disease. Pseudogenes of this gene are located on both the short and long arm of chromosome 3. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":45079288,"end":45305283,"strand":1,"description":"microtubule affinity regulating kinase 4 [Source:HGNC Symbol;Acc:HGNC:13538]"}, {"versioned_ensembl_gene_id":"ENSG00000224885.1","gene_symbol":"EIPR1-IT1","gene_name":"EIPR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41392]","synonyms":"TSSC1-IT1","biotype":"sense_intronic","ncbi_id":"100874301","summary":null,"start":3298341,"end":3301465,"strand":-1,"description":"EIPR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41392]"}, {"versioned_ensembl_gene_id":"ENSG00000196497.16","gene_symbol":"IPO4","gene_name":"importin 4 [Source:HGNC Symbol;Acc:HGNC:19426]","synonyms":"Imp4,FLJ23338","biotype":"protein_coding","ncbi_id":"79711","summary":null,"start":24180219,"end":24188964,"strand":-1,"description":"importin 4 [Source:HGNC Symbol;Acc:HGNC:19426]"}, {"versioned_ensembl_gene_id":"ENSG00000270503.1","gene_symbol":"YTHDF2P1","gene_name":"YTH domain family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19865]","synonyms":"YTHDF2P,NY-REN-2,HGRG8","biotype":"processed_pseudogene","ncbi_id":"400209","summary":null,"start":39215065,"end":39216335,"strand":1,"description":"YTH domain family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19865]"}, {"versioned_ensembl_gene_id":"ENSG00000242991.2","gene_symbol":"RPL7P40","gene_name":"ribosomal protein L7 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36031]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271220","summary":null,"start":17121716,"end":17122460,"strand":1,"description":"ribosomal protein L7 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36031]"}, {"versioned_ensembl_gene_id":"ENSG00000156755.10","gene_symbol":"IGKV1OR-2","gene_name":"immunoglobulin kappa variable 1/OR-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5761]","synonyms":"IGKVPZ2,IGKV1/OR-2","biotype":"IG_V_pseudogene","ncbi_id":"3532","summary":null,"start":64765054,"end":64765535,"strand":-1,"description":"immunoglobulin kappa variable 1/OR-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5761]"}, {"versioned_ensembl_gene_id":"ENSG00000171621.13","gene_symbol":"SPSB1","gene_name":"splA/ryanodine receptor domain and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:30628]","synonyms":"SSB-1","biotype":"protein_coding","ncbi_id":"80176","summary":null,"start":9292880,"end":9369532,"strand":1,"description":"splA/ryanodine receptor domain and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:30628]"}, {"versioned_ensembl_gene_id":"ENSG00000229220.1","gene_symbol":"AC096633.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":200147531,"end":200148279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107317.12","gene_symbol":"PTGDS","gene_name":"prostaglandin D2 synthase [Source:HGNC Symbol;Acc:HGNC:9592]","synonyms":"PGDS,L-PGDS","biotype":"protein_coding","ncbi_id":"5730","summary":"The protein encoded by this gene is a glutathione-independent prostaglandin D synthase that catalyzes the conversion of prostaglandin H2 (PGH2) to postaglandin D2 (PGD2). PGD2 functions as a neuromodulator as well as a trophic factor in the central nervous system. PGD2 is also involved in smooth muscle contraction/relaxation and is a potent inhibitor of platelet aggregation. This gene is preferentially expressed in brain. Studies with transgenic mice overexpressing this gene suggest that this gene may be also involved in the regulation of non-rapid eye movement sleep. [provided by RefSeq, Jul 2008]","start":136975092,"end":136981742,"strand":1,"description":"prostaglandin D2 synthase [Source:HGNC Symbol;Acc:HGNC:9592]"}, {"versioned_ensembl_gene_id":"ENSG00000174912.7","gene_symbol":"METTL15P1","gene_name":"methyltransferase like 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31926]","synonyms":"METT5D2","biotype":"processed_pseudogene","ncbi_id":"100130758","summary":null,"start":156713884,"end":156714928,"strand":-1,"description":"methyltransferase like 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31926]"}, {"versioned_ensembl_gene_id":"ENSG00000141376.22","gene_symbol":"BCAS3","gene_name":"BCAS3, microtubule associated cell migration factor [Source:HGNC Symbol;Acc:HGNC:14347]","synonyms":"FLJ20128","biotype":"protein_coding","ncbi_id":"54828","summary":null,"start":60677453,"end":61392838,"strand":1,"description":"BCAS3, microtubule associated cell migration factor [Source:HGNC Symbol;Acc:HGNC:14347]"}, {"versioned_ensembl_gene_id":"ENSG00000225181.1","gene_symbol":"AL121584.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15552157,"end":15552885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169599.12","gene_symbol":"NFU1","gene_name":"NFU1 iron-sulfur cluster scaffold [Source:HGNC Symbol;Acc:HGNC:16287]","synonyms":"NIFUC,NifU,HIRIP5,CGI-33","biotype":"protein_coding","ncbi_id":"27247","summary":"This gene encodes a protein that is localized to mitochondria and plays a critical role in iron-sulfur cluster biogenesis. The encoded protein assembles and transfers 4Fe-4S clusters to target apoproteins including succinate dehydrogenase and lipoic acid synthase. Mutations in this gene are a cause of multiple mitochondrial dysfunctions syndrome-1, and pseudogenes of this gene are located on the short arms of chromosomes 1 and 3. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":69395750,"end":69437628,"strand":-1,"description":"NFU1 iron-sulfur cluster scaffold [Source:HGNC Symbol;Acc:HGNC:16287]"}, {"versioned_ensembl_gene_id":"ENSG00000204481.7","gene_symbol":"PRAMEF14","gene_name":"PRAME family member 14 [Source:HGNC Symbol;Acc:HGNC:13576]","synonyms":"OTTHUMG00000007916","biotype":"protein_coding","ncbi_id":"729528","summary":null,"start":13342034,"end":13347134,"strand":-1,"description":"PRAME family member 14 [Source:HGNC Symbol;Acc:HGNC:13576]"}, {"versioned_ensembl_gene_id":"ENSG00000167074.14","gene_symbol":"TEF","gene_name":"TEF, PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:11722]","synonyms":"KIAA1655","biotype":"protein_coding","ncbi_id":"7008","summary":"This gene encodes a member of the PAR (proline and acidic amino acid-rich) subfamily of basic region/leucine zipper (bZIP) transcription factors. It is expressed in a broad range of cells and tissues in adult animals, however, during embryonic development, TEF expression appears to be restricted to the developing anterior pituitary gland, coincident with the appearance of thyroid-stimulating hormone, beta (TSHB). Indeed, TEF can bind to, and transactivate the TSHB promoter. It shows homology (in the functional domains) with other members of the PAR-bZIP subfamily of transcription factors, which include albumin D box-binding protein (DBP), human hepatic leukemia factor (HLF) and chicken vitellogenin gene-binding protein (VBP); VBP is considered the chicken homologue of TEF. Different members of the subfamily can readily form heterodimers, and share DNA-binding, and transcriptional regulatory properties. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":41367333,"end":41399326,"strand":1,"description":"TEF, PAR bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:11722]"}, {"versioned_ensembl_gene_id":"ENSG00000270569.1","gene_symbol":"AC068276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57429548,"end":57430693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172061.8","gene_symbol":"LRRC15","gene_name":"leucine rich repeat containing 15 [Source:HGNC Symbol;Acc:HGNC:20818]","synonyms":"LIB","biotype":"protein_coding","ncbi_id":"131578","summary":null,"start":194355247,"end":194369743,"strand":-1,"description":"leucine rich repeat containing 15 [Source:HGNC Symbol;Acc:HGNC:20818]"}, {"versioned_ensembl_gene_id":"ENSG00000253144.1","gene_symbol":"AC104117.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179082680,"end":179083194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226032.1","gene_symbol":"AL035530.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159064728,"end":159065273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273489.1","gene_symbol":"AC008264.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131493964,"end":131497694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128585.17","gene_symbol":"MKLN1","gene_name":"muskelin 1 [Source:HGNC Symbol;Acc:HGNC:7109]","synonyms":"TWA2","biotype":"protein_coding","ncbi_id":"4289","summary":"Muskelin is an intracellular protein that acts as a mediator of cell spreading and cytoskeletal responses to the extracellular matrix component thrombospondin I (MIM 188060) (Adams et al., 1998 [PubMed 9724633]).[supplied by OMIM, Mar 2008]","start":131110096,"end":131496636,"strand":1,"description":"muskelin 1 [Source:HGNC Symbol;Acc:HGNC:7109]"}, {"versioned_ensembl_gene_id":"ENSG00000274570.4","gene_symbol":"SPDYE10P","gene_name":"speedy/RINGO cell cycle regulator family member E10, pseudogene [Source:HGNC Symbol;Acc:HGNC:51506]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643862","summary":null,"start":73104201,"end":73111140,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E10, pseudogene [Source:HGNC Symbol;Acc:HGNC:51506]"}, {"versioned_ensembl_gene_id":"ENSG00000167964.12","gene_symbol":"RAB26","gene_name":"RAB26, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14259]","synonyms":null,"biotype":"protein_coding","ncbi_id":"25837","summary":"Members of the RAB protein family, including RAB26, are important regulators of vesicular fusion and trafficking. The RAB family of small G proteins regulates intercellular vesicle trafficking, including exocytosis, endocytosis, and recycling (summary by Seki et al., 2000 [PubMed 11043516]).[supplied by OMIM, Nov 2010]","start":2140803,"end":2154165,"strand":1,"description":"RAB26, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14259]"}, {"versioned_ensembl_gene_id":"ENSG00000226380.9","gene_symbol":"AC016831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130876809,"end":130913310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230745.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29965942,"end":29967605,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000110958.15","gene_symbol":"PTGES3","gene_name":"prostaglandin E synthase 3 [Source:HGNC Symbol;Acc:HGNC:16049]","synonyms":"TEBP,p23,cPGES","biotype":"protein_coding","ncbi_id":"10728","summary":"This gene encodes an enzyme that converts prostaglandin endoperoxide H2 (PGH2) to prostaglandin E2 (PGE2). This protein functions as a co-chaperone with heat shock protein 90 (HSP90), localizing to response elements in DNA and disrupting transcriptional activation complexes. Alternative splicing results in multiple transcript variants. There are multiple pseudogenes of this gene on several different chromosomes. [provided by RefSeq, Feb 2016]","start":56663341,"end":56688408,"strand":-1,"description":"prostaglandin E synthase 3 [Source:HGNC Symbol;Acc:HGNC:16049]"}, {"versioned_ensembl_gene_id":"ENSG00000282527.1","gene_symbol":"AC110491.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97800733,"end":97821884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249101.1","gene_symbol":"AC008834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98025965,"end":98026139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275976.4","gene_symbol":"SPDYE11","gene_name":"speedy/RINGO cell cycle regulator family member E11 [Source:HGNC Symbol;Acc:HGNC:51507]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100996746","summary":null,"start":73048055,"end":73057911,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E11 [Source:HGNC Symbol;Acc:HGNC:51507]"}, {"versioned_ensembl_gene_id":"ENSG00000273897.1","gene_symbol":"AC211476.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":73037371,"end":73049246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228507.1","gene_symbol":"DAP3P2","gene_name":"death associated protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29762]","synonyms":"MRPS29P2","biotype":"processed_pseudogene","ncbi_id":"359774","summary":null,"start":171491422,"end":171491931,"strand":1,"description":"death associated protein 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29762]"}, {"versioned_ensembl_gene_id":"ENSG00000234199.2","gene_symbol":"LINC01191","gene_name":"long intergenic non-protein coding RNA 1191 [Source:HGNC Symbol;Acc:HGNC:49595]","synonyms":"lnc-ACTR3,VIN","biotype":"lincRNA","ncbi_id":"440900","summary":null,"start":113979569,"end":114007302,"strand":1,"description":"long intergenic non-protein coding RNA 1191 [Source:HGNC Symbol;Acc:HGNC:49595]"}, {"versioned_ensembl_gene_id":"ENSG00000279401.1","gene_symbol":"AL133383.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":185518651,"end":185520986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196586.13","gene_symbol":"MYO6","gene_name":"myosin VI [Source:HGNC Symbol;Acc:HGNC:7605]","synonyms":"KIAA0389,DFNB37,DFNA22","biotype":"protein_coding","ncbi_id":"4646","summary":"This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":75749192,"end":75919537,"strand":1,"description":"myosin VI [Source:HGNC Symbol;Acc:HGNC:7605]"}, {"versioned_ensembl_gene_id":"ENSG00000276600.4","gene_symbol":"RAB7B","gene_name":"RAB7B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30513]","synonyms":"MGC9726,MGC16212","biotype":"protein_coding","ncbi_id":"338382","summary":null,"start":205976740,"end":206003461,"strand":-1,"description":"RAB7B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30513]"}, {"versioned_ensembl_gene_id":"ENSG00000113742.12","gene_symbol":"CPEB4","gene_name":"cytoplasmic polyadenylation element binding protein 4 [Source:HGNC Symbol;Acc:HGNC:21747]","synonyms":"KIAA1673","biotype":"protein_coding","ncbi_id":"80315","summary":null,"start":173888280,"end":173961976,"strand":1,"description":"cytoplasmic polyadenylation element binding protein 4 [Source:HGNC Symbol;Acc:HGNC:21747]"}, {"versioned_ensembl_gene_id":"ENSG00000176974.19","gene_symbol":"SHMT1","gene_name":"serine hydroxymethyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10850]","synonyms":"SHMT,MGC24556,MGC15229,CSHMT","biotype":"protein_coding","ncbi_id":"6470","summary":"This gene encodes the cytosolic form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one-carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. A pseudogene of this gene is located on the short arm of chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":18327860,"end":18363563,"strand":-1,"description":"serine hydroxymethyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10850]"}, {"versioned_ensembl_gene_id":"ENSG00000237359.1","gene_symbol":"AL354977.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3647335,"end":3648338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231219.1","gene_symbol":"PRAMEF32P","gene_name":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"650236","summary":null,"start":13273539,"end":13275627,"strand":-1,"description":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]"}, {"versioned_ensembl_gene_id":"ENSG00000124391.4","gene_symbol":"IL17C","gene_name":"interleukin 17C [Source:HGNC Symbol;Acc:HGNC:5983]","synonyms":"MGC138401,MGC126884,IL-21,IL-17C,CX2","biotype":"protein_coding","ncbi_id":"27189","summary":"The protein encoded by this gene is a T cell-derived cytokine that shares the sequence similarity with IL17. This cytokine was reported to stimulate the release of tumor necrosis factor alpha and interleukin 1 beta from a monocytic cell line. The expression of this cytokine was found to be restricted to activated T cells. [provided by RefSeq, Jul 2008]","start":88638591,"end":88640473,"strand":1,"description":"interleukin 17C [Source:HGNC Symbol;Acc:HGNC:5983]"}, {"versioned_ensembl_gene_id":"ENSG00000204913.5","gene_symbol":"LRRC3C","gene_name":"leucine rich repeat containing 3C [Source:HGNC Symbol;Acc:HGNC:40034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505591","summary":null,"start":39941474,"end":39944747,"strand":1,"description":"leucine rich repeat containing 3C [Source:HGNC Symbol;Acc:HGNC:40034]"}, {"versioned_ensembl_gene_id":"ENSG00000275183.1","gene_symbol":"LENG9","gene_name":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94059","summary":null,"start":54461796,"end":54463711,"strand":-1,"description":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]"}, {"versioned_ensembl_gene_id":"ENSG00000255469.1","gene_symbol":"BOLA3P1","gene_name":"bolA family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51440]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288111","summary":null,"start":102880492,"end":102880846,"strand":1,"description":"bolA family member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51440]"}, {"versioned_ensembl_gene_id":"ENSG00000117984.13","gene_symbol":"CTSD","gene_name":"cathepsin D [Source:HGNC Symbol;Acc:HGNC:2529]","synonyms":"CPSD,CLN10","biotype":"protein_coding","ncbi_id":"1509","summary":"This gene encodes a member of the A1 family of peptidases. The encoded preproprotein is proteolytically processed to generate multiple protein products. These products include the cathepsin D light and heavy chains, which heterodimerize to form the mature enzyme. This enzyme exhibits pepsin-like activity and plays a role in protein turnover and in the proteolytic activation of hormones and growth factors. Mutations in this gene play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases, including breast cancer and possibly Alzheimer's disease. [provided by RefSeq, Nov 2015]","start":1752752,"end":1764573,"strand":-1,"description":"cathepsin D [Source:HGNC Symbol;Acc:HGNC:2529]"}, {"versioned_ensembl_gene_id":"ENSG00000284682.1","gene_symbol":"AC078776.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":30306065,"end":30307611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103150.5","gene_symbol":"MLYCD","gene_name":"malonyl-CoA decarboxylase [Source:HGNC Symbol;Acc:HGNC:7150]","synonyms":"MCD,hMCD","biotype":"protein_coding","ncbi_id":"23417","summary":"The product of this gene catalyzes the breakdown of malonyl-CoA to acetyl-CoA and carbon dioxide. Malonyl-CoA is an intermediate in fatty acid biosynthesis, and also inhibits the transport of fatty acyl CoAs into mitochondria. Consequently, the encoded protein acts to increase the rate of fatty acid oxidation. It is found in mitochondria, peroxisomes, and the cytoplasm. Mutations in this gene result in malonyl-CoA decarboyxlase deficiency. [provided by RefSeq, Jul 2008]","start":83899126,"end":83927026,"strand":1,"description":"malonyl-CoA decarboxylase [Source:HGNC Symbol;Acc:HGNC:7150]"}, {"versioned_ensembl_gene_id":"ENSG00000180998.11","gene_symbol":"GPR137C","gene_name":"G protein-coupled receptor 137C [Source:HGNC Symbol;Acc:HGNC:25445]","synonyms":"TM7SF1L2,DKFZp762F0713","biotype":"protein_coding","ncbi_id":"283554","summary":null,"start":52553148,"end":52637713,"strand":1,"description":"G protein-coupled receptor 137C [Source:HGNC Symbol;Acc:HGNC:25445]"}, {"versioned_ensembl_gene_id":"ENSG00000017483.14","gene_symbol":"SLC38A5","gene_name":"solute carrier family 38 member 5 [Source:HGNC Symbol;Acc:HGNC:18070]","synonyms":"SN2,JM24","biotype":"protein_coding","ncbi_id":"92745","summary":"The protein encoded by this gene is a system N sodium-coupled amino acid transporter. The encoded protein transports glutamine, asparagine, histidine, serine, alanine, and glycine across the cell membrane, but does not transport charged amino acids, imino acids, or N-alkylated amino acids. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Aug 2013]","start":48458537,"end":48470256,"strand":-1,"description":"solute carrier family 38 member 5 [Source:HGNC Symbol;Acc:HGNC:18070]"}, {"versioned_ensembl_gene_id":"ENSG00000241598.5","gene_symbol":"KRTAP5-4","gene_name":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]","synonyms":"KRTAP5.4","biotype":"protein_coding","ncbi_id":"387267","summary":null,"start":1620958,"end":1622138,"strand":-1,"description":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]"}, {"versioned_ensembl_gene_id":"ENSG00000185860.13","gene_symbol":"CCDC190","gene_name":"coiled-coil domain containing 190 [Source:HGNC Symbol;Acc:HGNC:28736]","synonyms":"C1orf110,MGC48998","biotype":"protein_coding","ncbi_id":"339512","summary":null,"start":162824458,"end":162868815,"strand":-1,"description":"coiled-coil domain containing 190 [Source:HGNC Symbol;Acc:HGNC:28736]"}, {"versioned_ensembl_gene_id":"ENSG00000267452.1","gene_symbol":"LINC02073","gene_name":"long intergenic non-protein coding RNA 2073 [Source:HGNC Symbol;Acc:HGNC:52919]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371828","summary":null,"start":51435427,"end":51445802,"strand":1,"description":"long intergenic non-protein coding RNA 2073 [Source:HGNC Symbol;Acc:HGNC:52919]"}, {"versioned_ensembl_gene_id":"ENSG00000249383.1","gene_symbol":"LINC02071","gene_name":"long intergenic non-protein coding RNA 2071 [Source:HGNC Symbol;Acc:HGNC:52917]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927274","summary":null,"start":51312609,"end":51335165,"strand":-1,"description":"long intergenic non-protein coding RNA 2071 [Source:HGNC Symbol;Acc:HGNC:52917]"}, {"versioned_ensembl_gene_id":"ENSG00000256035.1","gene_symbol":"AP000619.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102806948,"end":102807916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232874.1","gene_symbol":"AC080129.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":194130616,"end":194131201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126945.8","gene_symbol":"HNRNPH2","gene_name":"heterogeneous nuclear ribonucleoprotein H2 [Source:HGNC Symbol;Acc:HGNC:5042]","synonyms":"HNRPH2,HNRPH',hnRNPH',FTP3","biotype":"protein_coding","ncbi_id":"3188","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that binds to RNAs. It is very similar to the family member HNRPH1. This gene is thought to be involved in Fabray disease and X-linked agammaglobulinemia phenotype. Alternative splicing results in multiple transcript variants encoding the same protein. Read-through transcription between this locus and the ribosomal protein L36a gene has been observed. [provided by RefSeq, Jan 2011]","start":101408295,"end":101414133,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein H2 [Source:HGNC Symbol;Acc:HGNC:5042]"}, {"versioned_ensembl_gene_id":"ENSG00000174586.10","gene_symbol":"ZNF497","gene_name":"zinc finger protein 497 [Source:HGNC Symbol;Acc:HGNC:23714]","synonyms":"FLJ44773","biotype":"protein_coding","ncbi_id":"162968","summary":null,"start":58354357,"end":58362848,"strand":-1,"description":"zinc finger protein 497 [Source:HGNC Symbol;Acc:HGNC:23714]"}, {"versioned_ensembl_gene_id":"ENSG00000251172.1","gene_symbol":"AC117470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97481177,"end":97481506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118113.11","gene_symbol":"MMP8","gene_name":"matrix metallopeptidase 8 [Source:HGNC Symbol;Acc:HGNC:7175]","synonyms":"CLG1","biotype":"protein_coding","ncbi_id":"4317","summary":"This gene encodes a member of the matrix metalloproteinase (MMP) family of proteins. These proteins are involved in the breakdown of extracellular matrix in embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Proteolysis at different sites on this protein results in multiple active forms of the enzyme with distinct N-termini. This protein functions in the degradation of type I, II and III collagens. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":102711795,"end":102727050,"strand":-1,"description":"matrix metallopeptidase 8 [Source:HGNC Symbol;Acc:HGNC:7175]"}, {"versioned_ensembl_gene_id":"ENSG00000232104.3","gene_symbol":"RFX3-AS1","gene_name":"RFX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51197]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929302","summary":null,"start":3526723,"end":3691814,"strand":1,"description":"RFX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51197]"}, {"versioned_ensembl_gene_id":"ENSG00000237238.2","gene_symbol":"BMS1P10","gene_name":"BMS1, ribosome biogenesis factor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49154]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728611","summary":null,"start":63372803,"end":63380011,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49154]"}, {"versioned_ensembl_gene_id":"ENSG00000138435.15","gene_symbol":"CHRNA1","gene_name":"cholinergic receptor nicotinic alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:1955]","synonyms":"CHRNA","biotype":"protein_coding","ncbi_id":"1134","summary":"The muscle acetylcholine receptor consiststs of 5 subunits of 4 different types: 2 alpha subunits and 1 each of the beta, gamma, and delta subunits. This gene encodes an alpha subunit that plays a role in acetlycholine binding/channel gating. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Nov 2012]","start":174747592,"end":174787935,"strand":-1,"description":"cholinergic receptor nicotinic alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:1955]"}, {"versioned_ensembl_gene_id":"ENSG00000276115.1","gene_symbol":"AC026356.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32352349,"end":32354144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113368.11","gene_symbol":"LMNB1","gene_name":"lamin B1 [Source:HGNC Symbol;Acc:HGNC:6637]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4001","summary":"This gene encodes one of the two B-type lamin proteins and is a component of the nuclear lamina. A duplication of this gene is associated with autosomal dominant adult-onset leukodystrophy (ADLD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":126776623,"end":126837020,"strand":1,"description":"lamin B1 [Source:HGNC Symbol;Acc:HGNC:6637]"}, {"versioned_ensembl_gene_id":"ENSG00000115267.5","gene_symbol":"IFIH1","gene_name":"interferon induced with helicase C domain 1 [Source:HGNC Symbol;Acc:HGNC:18873]","synonyms":"MDA5,MDA-5,IDDM19,Hlcd","biotype":"protein_coding","ncbi_id":"64135","summary":"IFIH1 encodes MDA5 which is an intracellular sensor of viral RNA that triggers the innate immune response. Sensing RNA length and secondary structure, MDA5 binds dsRNA oligonucleotides with a modified DExD/H-box helicase core and a C-terminal domain, thus leading to a proinflammatory response that includes interferons. It has been shown that Coronaviruses (CoVs) as well as various other virus families, are capable of evading the MDA5-dependent interferon response, thus impeding the activation of the innate immune response to infection. MDA5 has also been shown to play an important role in enhancing natural killer cell function in malaria infection. In addition to its protective role in antiviral responses, MDA5 has been implicated in autoimmune and autoinflammatory diseases such as type 1 diabetes, systemic lupus erythematosus, and Aicardi-Goutieres syndrome[provided by RefSeq, Jul 2020]","start":162267079,"end":162318703,"strand":-1,"description":"interferon induced with helicase C domain 1 [Source:HGNC Symbol;Acc:HGNC:18873]"}, {"versioned_ensembl_gene_id":"ENSG00000184545.10","gene_symbol":"DUSP8","gene_name":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]","synonyms":"HB5,FLJ42958,C11orf81,HVH-5","biotype":"protein_coding","ncbi_id":"1850","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates SAPK/JNK and p38, is expressed predominantly in the adult brain, heart, and skeletal muscle, is localized in the cytoplasm, and is induced by nerve growth factor and insulin. An intronless pseudogene for DUSP8 is present on chromosome 10q11.2. [provided by RefSeq, Jul 2008]","start":1554044,"end":1571920,"strand":-1,"description":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]"}, {"versioned_ensembl_gene_id":"ENSG00000150760.12","gene_symbol":"DOCK1","gene_name":"dedicator of cytokinesis 1 [Source:HGNC Symbol;Acc:HGNC:2987]","synonyms":"DOCK180,ced5","biotype":"protein_coding","ncbi_id":"1793","summary":"This gene encodes a member of the dedicator of cytokinesis protein family. Dedicator of cytokinesis proteins act as guanine nucleotide exchange factors for small Rho family G proteins. The encoded protein regulates the small GTPase Rac, thereby influencing several biological processes, including phagocytosis and cell migration. Overexpression of this gene has also been associated with certain cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":126905409,"end":127452517,"strand":1,"description":"dedicator of cytokinesis 1 [Source:HGNC Symbol;Acc:HGNC:2987]"}, {"versioned_ensembl_gene_id":"ENSG00000167283.7","gene_symbol":"ATP5L","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G [Source:HGNC Symbol;Acc:HGNC:14247]","synonyms":"ATP5JG","biotype":"protein_coding","ncbi_id":"10632","summary":"Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the g subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]","start":118401154,"end":118431496,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G [Source:HGNC Symbol;Acc:HGNC:14247]"}, {"versioned_ensembl_gene_id":"ENSG00000133313.14","gene_symbol":"CNDP2","gene_name":"carnosine dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24437]","synonyms":"PEPA,HsT2298,FLJ10830,CPGL,CN2","biotype":"protein_coding","ncbi_id":"55748","summary":"CNDP2, also known as tissue carnosinase and peptidase A (EC 3.4.13.18), is a nonspecific dipeptidase rather than a selective carnosinase (Teufel et al., 2003 [PubMed 12473676]).[supplied by OMIM, Mar 2008]","start":74495816,"end":74523454,"strand":1,"description":"carnosine dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:24437]"}, {"versioned_ensembl_gene_id":"ENSG00000011258.15","gene_symbol":"MBTD1","gene_name":"mbt domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19866]","synonyms":"SA49P01,FLJ20055","biotype":"protein_coding","ncbi_id":"54799","summary":null,"start":51177425,"end":51260163,"strand":-1,"description":"mbt domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19866]"}, {"versioned_ensembl_gene_id":"ENSG00000251513.2","gene_symbol":"LIX1-AS1","gene_name":"LIX1 and RIOK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52976]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926893","summary":null,"start":97089075,"end":97437217,"strand":1,"description":"LIX1 and RIOK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52976]"}, {"versioned_ensembl_gene_id":"ENSG00000227407.1","gene_symbol":"AC245884.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54430654,"end":54434698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169154.5","gene_symbol":"GOT1L1","gene_name":"glutamic-oxaloacetic transaminase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28487]","synonyms":"MGC33309","biotype":"protein_coding","ncbi_id":"137362","summary":null,"start":37934281,"end":37940129,"strand":-1,"description":"glutamic-oxaloacetic transaminase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28487]"}, {"versioned_ensembl_gene_id":"ENSG00000010704.18","gene_symbol":"HFE","gene_name":"hemochromatosis [Source:HGNC Symbol;Acc:HGNC:4886]","synonyms":"HLA-H","biotype":"protein_coding","ncbi_id":"3077","summary":"The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":26087281,"end":26098343,"strand":1,"description":"hemochromatosis [Source:HGNC Symbol;Acc:HGNC:4886]"}, {"versioned_ensembl_gene_id":"ENSG00000229018.5","gene_symbol":"PMS2P7","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33515]","synonyms":"PMSR7,PMS2LP2,PMS2L15","biotype":"unprocessed_pseudogene","ncbi_id":"100101440","summary":null,"start":73005541,"end":73021103,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33515]"}, {"versioned_ensembl_gene_id":"ENSG00000146094.13","gene_symbol":"DOK3","gene_name":"docking protein 3 [Source:HGNC Symbol;Acc:HGNC:24583]","synonyms":"FLJ22570","biotype":"protein_coding","ncbi_id":"79930","summary":null,"start":177501907,"end":177511274,"strand":-1,"description":"docking protein 3 [Source:HGNC Symbol;Acc:HGNC:24583]"}, {"versioned_ensembl_gene_id":"ENSG00000106018.13","gene_symbol":"VIPR2","gene_name":"vasoactive intestinal peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:12695]","synonyms":"VPAC2R,VPAC2","biotype":"protein_coding","ncbi_id":"7434","summary":"This gene encodes a receptor for vasoactive intestinal peptide, a small neuropeptide. Vasoactive intestinal peptide is involved in smooth muscle relaxation, exocrine and endocrine secretion, and water and ion flux in lung and intestinal epithelia. Its actions are effected through integral membrane receptors associated with a guanine nucleotide binding protein which activates adenylate cyclase. [provided by RefSeq, Aug 2011]","start":159028175,"end":159144957,"strand":-1,"description":"vasoactive intestinal peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:12695]"}, {"versioned_ensembl_gene_id":"ENSG00000278637.1","gene_symbol":"HIST1H4A","gene_name":"histone cluster 1 H4 family member a [Source:HGNC Symbol;Acc:HGNC:4781]","synonyms":"H4FA","biotype":"protein_coding","ncbi_id":"8359","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26021679,"end":26021990,"strand":1,"description":"histone cluster 1 H4 family member a [Source:HGNC Symbol;Acc:HGNC:4781]"}, {"versioned_ensembl_gene_id":"ENSG00000233099.1","gene_symbol":"AC095030.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77346046,"end":77349585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275714.1","gene_symbol":"HIST1H3A","gene_name":"histone cluster 1 H3 family member a [Source:HGNC Symbol;Acc:HGNC:4766]","synonyms":"H3FA,H3/A","biotype":"protein_coding","ncbi_id":"8350","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26020490,"end":26020900,"strand":1,"description":"histone cluster 1 H3 family member a [Source:HGNC Symbol;Acc:HGNC:4766]"}, {"versioned_ensembl_gene_id":"ENSG00000066135.12","gene_symbol":"KDM4A","gene_name":"lysine demethylase 4A [Source:HGNC Symbol;Acc:HGNC:22978]","synonyms":"KIAA0677,JMJD2A,JMJD2,JHDM3A,TDRD14A","biotype":"protein_coding","ncbi_id":"9682","summary":"This gene is a member of the Jumonji domain 2 (JMJD2) family and encodes a protein containing a JmjN domain, a JmjC domain, a JD2H domain, two TUDOR domains, and two PHD-type zinc fingers. This nuclear protein functions as a trimethylation-specific demethylase, converting specific trimethylated histone residues to the dimethylated form, and as a transcriptional repressor. [provided by RefSeq, Apr 2009]","start":43650158,"end":43705515,"strand":1,"description":"lysine demethylase 4A [Source:HGNC Symbol;Acc:HGNC:22978]"}, {"versioned_ensembl_gene_id":"ENSG00000186891.13","gene_symbol":"TNFRSF18","gene_name":"TNF receptor superfamily member 18 [Source:HGNC Symbol;Acc:HGNC:11914]","synonyms":"GITR,CD357,AITR","biotype":"protein_coding","ncbi_id":"8784","summary":"This gene encodes a member of the TNF-receptor superfamily. The encoded receptor has been shown to have increased expression upon T-cell activation, and it is thought to play a key role in dominant immunological self-tolerance maintained by CD25(+)CD4(+) regulatory T cells. Knockout studies in mice also suggest the role of this receptor is in the regulation of CD3-driven T-cell activation and programmed cell death. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Feb 2011]","start":1203508,"end":1206691,"strand":-1,"description":"TNF receptor superfamily member 18 [Source:HGNC Symbol;Acc:HGNC:11914]"}, {"versioned_ensembl_gene_id":"ENSG00000188306.6","gene_symbol":"LRRIQ4","gene_name":"leucine rich repeats and IQ motif containing 4 [Source:HGNC Symbol;Acc:HGNC:34298]","synonyms":"LRRC64","biotype":"protein_coding","ncbi_id":"344657","summary":null,"start":169821922,"end":169837775,"strand":1,"description":"leucine rich repeats and IQ motif containing 4 [Source:HGNC Symbol;Acc:HGNC:34298]"}, {"versioned_ensembl_gene_id":"ENSG00000167619.11","gene_symbol":"TMEM145","gene_name":"transmembrane protein 145 [Source:HGNC Symbol;Acc:HGNC:26912]","synonyms":"FLJ90805","biotype":"protein_coding","ncbi_id":"284339","summary":null,"start":42313325,"end":42325062,"strand":1,"description":"transmembrane protein 145 [Source:HGNC Symbol;Acc:HGNC:26912]"}, {"versioned_ensembl_gene_id":"ENSG00000135299.16","gene_symbol":"ANKRD6","gene_name":"ankyrin repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:17280]","synonyms":"KIAA0957","biotype":"protein_coding","ncbi_id":"22881","summary":null,"start":89433170,"end":89633834,"strand":1,"description":"ankyrin repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:17280]"}, {"versioned_ensembl_gene_id":"ENSG00000251654.2","gene_symbol":"AC099499.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25218973,"end":25298612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164107.8","gene_symbol":"HAND2","gene_name":"heart and neural crest derivatives expressed 2 [Source:HGNC Symbol;Acc:HGNC:4808]","synonyms":"Thing2,Hed,dHand,bHLHa26","biotype":"protein_coding","ncbi_id":"9464","summary":"The protein encoded by this gene belongs to the basic helix-loop-helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, this transcription factor plays an important role in limb and branchial arch development. [provided by RefSeq, Jul 2008]","start":173524969,"end":173530229,"strand":-1,"description":"heart and neural crest derivatives expressed 2 [Source:HGNC Symbol;Acc:HGNC:4808]"}, {"versioned_ensembl_gene_id":"ENSG00000253347.1","gene_symbol":"AC040934.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47409322,"end":47423526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123095.5","gene_symbol":"BHLHE41","gene_name":"basic helix-loop-helix family member e41 [Source:HGNC Symbol;Acc:HGNC:16617]","synonyms":"SHARP1,SHARP-1,DEC2,bHLHe41,BHLHB3","biotype":"protein_coding","ncbi_id":"79365","summary":"This gene encodes a basic helix-loop-helix protein expressed in various tissues. The encoded protein can interact with ARNTL or compete for E-box binding sites in the promoter of PER1 and repress CLOCK/ARNTL's transactivation of PER1. This gene is believed to be involved in the control of circadian rhythm and cell differentiation. Defects in this gene are associated with the short sleep phenotype. [provided by RefSeq, Feb 2014]","start":26120026,"end":26125127,"strand":-1,"description":"basic helix-loop-helix family member e41 [Source:HGNC Symbol;Acc:HGNC:16617]"}, {"versioned_ensembl_gene_id":"ENSG00000178342.4","gene_symbol":"KCNG2","gene_name":"potassium voltage-gated channel modifier subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:6249]","synonyms":"Kv6.2,KCNF2","biotype":"protein_coding","ncbi_id":"26251","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This member is a gamma subunit of the voltage-gated potassium channel. The delayed-rectifier type channels containing this subunit may contribute to cardiac action potential repolarization. [provided by RefSeq, Jul 2008]","start":79863668,"end":79900184,"strand":1,"description":"potassium voltage-gated channel modifier subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:6249]"}, {"versioned_ensembl_gene_id":"ENSG00000238116.2","gene_symbol":"Z95327.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100801188,"end":100803060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204501.7","gene_symbol":"PRAMEF15","gene_name":"PRAME family member 15 [Source:HGNC Symbol;Acc:HGNC:26764]","synonyms":"OTTHUMG00000007921","biotype":"protein_coding","ncbi_id":"653619","summary":null,"start":13315581,"end":13322598,"strand":1,"description":"PRAME family member 15 [Source:HGNC Symbol;Acc:HGNC:26764]"}, {"versioned_ensembl_gene_id":"ENSG00000139266.5","gene_symbol":"MARCH9","gene_name":"membrane associated ring-CH-type finger 9 [Source:HGNC Symbol;Acc:HGNC:25139]","synonyms":"RNF179,FLJ36578","biotype":"protein_coding","ncbi_id":"92979","summary":"MARCH9 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH9 induces internalization of several membrane glycoproteins and directs them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Hoer et al., 2007 [PubMed 17174307]).[supplied by OMIM, Apr 2010]","start":57755098,"end":57760407,"strand":1,"description":"membrane associated ring-CH-type finger 9 [Source:HGNC Symbol;Acc:HGNC:25139]"}, {"versioned_ensembl_gene_id":"ENSG00000108423.14","gene_symbol":"TUBD1","gene_name":"tubulin delta 1 [Source:HGNC Symbol;Acc:HGNC:16811]","synonyms":"TUBD,FLJ12709","biotype":"protein_coding","ncbi_id":"51174","summary":null,"start":59859482,"end":59892945,"strand":-1,"description":"tubulin delta 1 [Source:HGNC Symbol;Acc:HGNC:16811]"}, {"versioned_ensembl_gene_id":"ENSG00000137197.6","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31107584,"end":31112941,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000233739.1","gene_symbol":"AL031587.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38057180,"end":38073940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214351.5","gene_symbol":"OR1X5P","gene_name":"olfactory receptor family 1 subfamily X member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31245]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402240","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":177836434,"end":177837646,"strand":-1,"description":"olfactory receptor family 1 subfamily X member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31245]"}, {"versioned_ensembl_gene_id":"ENSG00000283103.1","gene_symbol":"AC010642.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58310449,"end":58326933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142396.10","gene_symbol":"AC020915.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":58305319,"end":58315663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049323.15","gene_symbol":"LTBP1","gene_name":"latent transforming growth factor beta binding protein 1 [Source:HGNC Symbol;Acc:HGNC:6714]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4052","summary":"The protein encoded by this gene belongs to the family of latent TGF-beta binding proteins (LTBPs). The secretion and activation of TGF-betas is regulated by their association with latency-associated proteins and with latent TGF-beta binding proteins. The product of this gene targets latent complexes of transforming growth factor beta to the extracellular matrix, where the latent cytokine is subsequently activated by several different mechanisms. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":32946972,"end":33399509,"strand":1,"description":"latent transforming growth factor beta binding protein 1 [Source:HGNC Symbol;Acc:HGNC:6714]"}, {"versioned_ensembl_gene_id":"ENSG00000226608.3","gene_symbol":"FTLP3","gene_name":"ferritin light chain pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4000]","synonyms":"FTLL1,dJ681N20.2","biotype":"processed_pseudogene","ncbi_id":"284764","summary":null,"start":4023917,"end":4024444,"strand":1,"description":"ferritin light chain pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4000]"}, {"versioned_ensembl_gene_id":"ENSG00000249109.1","gene_symbol":"AC140125.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177782197,"end":177794396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198312.4","gene_symbol":"BMS1P9","gene_name":"BMS1, ribosome biogenesis factor pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49155]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653458","summary":null,"start":63055641,"end":63059217,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49155]"}, {"versioned_ensembl_gene_id":"ENSG00000204487.8","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"p33,TNFSF3,TNFC","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31567961,"end":31569928,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000163507.13","gene_symbol":"KIAA1524","gene_name":"KIAA1524 [Source:HGNC Symbol;Acc:HGNC:29302]","synonyms":"CIP2A","biotype":"protein_coding","ncbi_id":"57650","summary":null,"start":108549869,"end":108589644,"strand":-1,"description":"KIAA1524 [Source:HGNC Symbol;Acc:HGNC:29302]"}, {"versioned_ensembl_gene_id":"ENSG00000140522.11","gene_symbol":"RLBP1","gene_name":"retinaldehyde binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10024]","synonyms":"CRALBP","biotype":"protein_coding","ncbi_id":"6017","summary":"The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens. [provided by RefSeq, Jul 2008]","start":89209869,"end":89221751,"strand":-1,"description":"retinaldehyde binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10024]"}, {"versioned_ensembl_gene_id":"ENSG00000233352.1","gene_symbol":"AL035660.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45229817,"end":45230191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223772.1","gene_symbol":"GEMIN8P3","gene_name":"gem nuclear organelle associated protein 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421535","summary":null,"start":86304367,"end":86305086,"strand":1,"description":"gem nuclear organelle associated protein 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37978]"}, {"versioned_ensembl_gene_id":"ENSG00000169139.11","gene_symbol":"UBE2V2","gene_name":"ubiquitin conjugating enzyme E2 V2 [Source:HGNC Symbol;Acc:HGNC:12495]","synonyms":"DDVIT1,DDVit-1,UEV2,UEV-2,MMS2,EDPF1,EDPF-1,EDAF-1","biotype":"protein_coding","ncbi_id":"7336","summary":"Ubiquitin-conjugating enzyme E2 variant proteins constitute a distinct subfamily within the E2 protein family. They have sequence similarity to other ubiquitin-conjugating enzymes but lack the conserved cysteine residue that is critical for the catalytic activity of E2s. The protein encoded by this gene also shares homology with ubiquitin-conjugating enzyme E2 variant 1 and yeast MMS2 gene product. It may be involved in the differentiation of monocytes and enterocytes. [provided by RefSeq, Jul 2008]","start":48008400,"end":48064708,"strand":1,"description":"ubiquitin conjugating enzyme E2 V2 [Source:HGNC Symbol;Acc:HGNC:12495]"}, {"versioned_ensembl_gene_id":"ENSG00000100154.14","gene_symbol":"TTC28","gene_name":"tetratricopeptide repeat domain 28 [Source:HGNC Symbol;Acc:HGNC:29179]","synonyms":"KIAA1043","biotype":"protein_coding","ncbi_id":"23331","summary":null,"start":27978014,"end":28679865,"strand":-1,"description":"tetratricopeptide repeat domain 28 [Source:HGNC Symbol;Acc:HGNC:29179]"}, {"versioned_ensembl_gene_id":"ENSG00000249286.1","gene_symbol":"AMD1P3","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728931","summary":null,"start":43586918,"end":43588223,"strand":-1,"description":"adenosylmethionine decarboxylase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51608]"}, {"versioned_ensembl_gene_id":"ENSG00000229295.11","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33230030,"end":33241311,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000233972.1","gene_symbol":"CR847849.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33233561,"end":33233970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236375.3","gene_symbol":"POU5F1P5","gene_name":"POU class 5 homeobox 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33311]","synonyms":"Oct4-pg5","biotype":"processed_pseudogene","ncbi_id":"100009667","summary":null,"start":68010205,"end":68010862,"strand":-1,"description":"POU class 5 homeobox 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33311]"}, {"versioned_ensembl_gene_id":"ENSG00000230040.1","gene_symbol":"LINC00364","gene_name":"long intergenic non-protein coding RNA 364 [Source:HGNC Symbol;Acc:HGNC:42686]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874145","summary":null,"start":67372387,"end":67379976,"strand":1,"description":"long intergenic non-protein coding RNA 364 [Source:HGNC Symbol;Acc:HGNC:42686]"}, {"versioned_ensembl_gene_id":"ENSG00000214976.2","gene_symbol":"VDAC2P1","gene_name":"voltage dependent anion channel 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12673]","synonyms":"VDAC2P","biotype":"processed_pseudogene","ncbi_id":"54015","summary":null,"start":16094415,"end":16095372,"strand":-1,"description":"voltage dependent anion channel 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12673]"}, {"versioned_ensembl_gene_id":"ENSG00000155719.16","gene_symbol":"OTOA","gene_name":"otoancorin [Source:HGNC Symbol;Acc:HGNC:16378]","synonyms":"DFNB22,CT108","biotype":"protein_coding","ncbi_id":"146183","summary":"The protein encoded by this gene is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":21678514,"end":21760729,"strand":1,"description":"otoancorin [Source:HGNC Symbol;Acc:HGNC:16378]"}, {"versioned_ensembl_gene_id":"ENSG00000261915.6","gene_symbol":"AC026954.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7312661,"end":7319174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231206.2","gene_symbol":"HNRNPA1P25","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39543]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131983","summary":null,"start":74473017,"end":74473953,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39543]"}, {"versioned_ensembl_gene_id":"ENSG00000180957.17","gene_symbol":"PITPNB","gene_name":"phosphatidylinositol transfer protein beta [Source:HGNC Symbol;Acc:HGNC:9002]","synonyms":"VIB1B","biotype":"protein_coding","ncbi_id":"23760","summary":"This gene encodes a cytoplasmic protein that catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes. This transfer activity is required for COPI complex-mediated retrograde transport from the Golgi apparatus to the endoplasmic reticulum. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":27851669,"end":27920134,"strand":-1,"description":"phosphatidylinositol transfer protein beta [Source:HGNC Symbol;Acc:HGNC:9002]"}, {"versioned_ensembl_gene_id":"ENSG00000180398.11","gene_symbol":"MCFD2","gene_name":"multiple coagulation factor deficiency 2 [Source:HGNC Symbol;Acc:HGNC:18451]","synonyms":"SDNSF,LMAN1IP,F5F8D","biotype":"protein_coding","ncbi_id":"90411","summary":"This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2016]","start":46901870,"end":46941855,"strand":-1,"description":"multiple coagulation factor deficiency 2 [Source:HGNC Symbol;Acc:HGNC:18451]"}, {"versioned_ensembl_gene_id":"ENSG00000107262.19","gene_symbol":"BAG1","gene_name":"BCL2 associated athanogene 1 [Source:HGNC Symbol;Acc:HGNC:937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"573","summary":"The oncogene BCL2 is a membrane protein that blocks a step in a pathway leading to apoptosis or programmed cell death. The protein encoded by this gene binds to BCL2 and is referred to as BCL2-associated athanogene. It enhances the anti-apoptotic effects of BCL2 and represents a link between growth factor receptors and anti-apoptotic mechanisms. Multiple protein isoforms are encoded by this mRNA through the use of a non-AUG (CUG) initiation codon, and three alternative downstream AUG initiation codons. A related pseudogene has been defined on chromosome X. [provided by RefSeq, Feb 2010]","start":33247820,"end":33264720,"strand":-1,"description":"BCL2 associated athanogene 1 [Source:HGNC Symbol;Acc:HGNC:937]"}, {"versioned_ensembl_gene_id":"ENSG00000223454.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"processed_transcript","ncbi_id":"102723346","summary":null,"start":30935673,"end":30944555,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000232308.4","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"bCX105N19.6,PBLT,C6orf37","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":30930703,"end":30943914,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000228187.1","gene_symbol":"AC093433.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77194825,"end":77195395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235422.1","gene_symbol":"KATNBL1P3","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49053]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420946","summary":null,"start":2593674,"end":2594913,"strand":-1,"description":"katanin regulatory subunit B1 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49053]"}, {"versioned_ensembl_gene_id":"ENSG00000244081.1","gene_symbol":"AL591379.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63025597,"end":63025993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143106.12","gene_symbol":"PSMA5","gene_name":"proteasome subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:9534]","synonyms":"ZETA","biotype":"protein_coding","ncbi_id":"5686","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. Multiple alternatively spliced transcript variants encoding two distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":109399031,"end":109426427,"strand":-1,"description":"proteasome subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:9534]"}, {"versioned_ensembl_gene_id":"ENSG00000239672.7","gene_symbol":"NME1","gene_name":"NME/NM23 nucleoside diphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:7849]","synonyms":"NM23-H1,NM23,NDPKA","biotype":"protein_coding","ncbi_id":"4830","summary":"This gene (NME1) was identified because of its reduced mRNA transcript levels in highly metastatic cells. Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by this gene) and 'B' (encoded by NME2) isoforms. Mutations in this gene have been identified in aggressive neuroblastomas. Two transcript variants encoding different isoforms have been found for this gene. Co-transcription of this gene and the neighboring downstream gene (NME2) generates naturally-occurring transcripts (NME1-NME2), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Jul 2008]","start":51153536,"end":51162428,"strand":1,"description":"NME/NM23 nucleoside diphosphate kinase 1 [Source:HGNC Symbol;Acc:HGNC:7849]"}, {"versioned_ensembl_gene_id":"ENSG00000175315.2","gene_symbol":"CST6","gene_name":"cystatin E/M [Source:HGNC Symbol;Acc:HGNC:2478]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1474","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. This gene encodes a cystatin from the type 2 family, which is down-regulated in metastatic breast tumor cells as compared to primary tumor cells. Loss of expression is likely associated with the progression of a primary tumor to a metastatic phenotype. [provided by RefSeq, Jul 2008]","start":66011841,"end":66013505,"strand":1,"description":"cystatin E/M [Source:HGNC Symbol;Acc:HGNC:2478]"}, {"versioned_ensembl_gene_id":"ENSG00000152082.13","gene_symbol":"MZT2B","gene_name":"mitotic spindle organizing protein 2B [Source:HGNC Symbol;Acc:HGNC:25886]","synonyms":"MOZART2B,FLJ14346,FAM128B","biotype":"protein_coding","ncbi_id":"80097","summary":null,"start":130181737,"end":130190729,"strand":1,"description":"mitotic spindle organizing protein 2B [Source:HGNC Symbol;Acc:HGNC:25886]"}, {"versioned_ensembl_gene_id":"ENSG00000265126.1","gene_symbol":"AC004448.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19411786,"end":19413118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141028.6","gene_symbol":"CDRT15P1","gene_name":"CMT1A duplicated region transcript 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33168]","synonyms":"CDRT15P","biotype":"unprocessed_pseudogene","ncbi_id":"94158","summary":null,"start":14024514,"end":14025488,"strand":1,"description":"CMT1A duplicated region transcript 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33168]"}, {"versioned_ensembl_gene_id":"ENSG00000205360.6","gene_symbol":"MT1CP","gene_name":"metallothionein 1C, pseudogene [Source:HGNC Symbol;Acc:HGNC:7395]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441771","summary":null,"start":56648248,"end":56649514,"strand":1,"description":"metallothionein 1C, pseudogene [Source:HGNC Symbol;Acc:HGNC:7395]"}, {"versioned_ensembl_gene_id":"ENSG00000073921.17","gene_symbol":"PICALM","gene_name":"phosphatidylinositol binding clathrin assembly protein [Source:HGNC Symbol;Acc:HGNC:15514]","synonyms":"CLTH,CALM","biotype":"protein_coding","ncbi_id":"8301","summary":"This gene encodes a clathrin assembly protein, which recruits clathrin and adaptor protein complex 2 (AP2) to cell membranes at sites of coated-pit formation and clathrin-vesicle assembly. The protein may be required to determine the amount of membrane to be recycled, possibly by regulating the size of the clathrin cage. The protein is involved in AP2-dependent clathrin-mediated endocytosis at the neuromuscular junction. A chromosomal translocation t(10;11)(p13;q14) leading to the fusion of this gene and the MLLT10 gene is found in acute lymphoblastic leukemia, acute myeloid leukemia and malignant lymphomas. The polymorphisms of this gene are associated with the risk of Alzheimer disease. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":85957684,"end":86069882,"strand":-1,"description":"phosphatidylinositol binding clathrin assembly protein [Source:HGNC Symbol;Acc:HGNC:15514]"}, {"versioned_ensembl_gene_id":"ENSG00000266002.1","gene_symbol":"AC091059.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59400488,"end":59403303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239332.5","gene_symbol":"LINC01119","gene_name":"long intergenic non-protein coding RNA 1119 [Source:HGNC Symbol;Acc:HGNC:49262]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100134259","summary":null,"start":46816697,"end":46859007,"strand":1,"description":"long intergenic non-protein coding RNA 1119 [Source:HGNC Symbol;Acc:HGNC:49262]"}, {"versioned_ensembl_gene_id":"ENSG00000232401.1","gene_symbol":"LINC00112","gene_name":"long intergenic non-protein coding RNA 112 [Source:HGNC Symbol;Acc:HGNC:1263]","synonyms":"NCRNA00112,C21orf22","biotype":"antisense_RNA","ncbi_id":"54089","summary":null,"start":41716436,"end":41717580,"strand":1,"description":"long intergenic non-protein coding RNA 112 [Source:HGNC Symbol;Acc:HGNC:1263]"}, {"versioned_ensembl_gene_id":"ENSG00000275116.1","gene_symbol":"CU457734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54229470,"end":54230647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271063.1","gene_symbol":"SNRPGP17","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49372]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481685","summary":null,"start":59281130,"end":59281343,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49372]"}, {"versioned_ensembl_gene_id":"ENSG00000132522.15","gene_symbol":"GPS2","gene_name":"G protein pathway suppressor 2 [Source:HGNC Symbol;Acc:HGNC:4550]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2874","summary":"This gene encodes a protein involved in G protein-mitogen-activated protein kinase (MAPK) signaling cascades. When overexpressed in mammalian cells, this gene could potently suppress a RAS- and MAPK-mediated signal and interfere with JNK activity, suggesting that the function of this gene may be signal repression. The encoded protein is an integral subunit of the NCOR1-HDAC3 (nuclear receptor corepressor 1-histone deacetylase 3) complex, and it was shown that the complex inhibits JNK activation through this subunit and thus could potentially provide an alternative mechanism for hormone-mediated antagonism of AP1 (activator protein 1) function. [provided by RefSeq, Jul 2008]","start":7311324,"end":7315564,"strand":-1,"description":"G protein pathway suppressor 2 [Source:HGNC Symbol;Acc:HGNC:4550]"}, {"versioned_ensembl_gene_id":"ENSG00000283293.1","gene_symbol":"RN7SK","gene_name":"RNA, 7SK small nuclear [Source:HGNC Symbol;Acc:HGNC:10037]","synonyms":"7SK","biotype":"snRNA","ncbi_id":"125050","summary":null,"start":52995621,"end":52995948,"strand":1,"description":"RNA, 7SK small nuclear [Source:HGNC Symbol;Acc:HGNC:10037]"}, {"versioned_ensembl_gene_id":"ENSG00000213269.2","gene_symbol":"AC004386.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74376125,"end":74376885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226515.1","gene_symbol":"AC004386.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74342713,"end":74342860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167771.5","gene_symbol":"RCOR2","gene_name":"REST corepressor 2 [Source:HGNC Symbol;Acc:HGNC:27455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283248","summary":null,"start":63911221,"end":63916844,"strand":-1,"description":"REST corepressor 2 [Source:HGNC Symbol;Acc:HGNC:27455]"}, {"versioned_ensembl_gene_id":"ENSG00000228073.1","gene_symbol":"AC133106.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":189095063,"end":189096158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189306.10","gene_symbol":"RRP7A","gene_name":"ribosomal RNA processing 7 homolog A [Source:HGNC Symbol;Acc:HGNC:24286]","synonyms":"Rrp7,CGI-96","biotype":"protein_coding","ncbi_id":"27341","summary":null,"start":42509968,"end":42519802,"strand":-1,"description":"ribosomal RNA processing 7 homolog A [Source:HGNC Symbol;Acc:HGNC:24286]"}, {"versioned_ensembl_gene_id":"ENSG00000105227.14","gene_symbol":"PRX","gene_name":"periaxin [Source:HGNC Symbol;Acc:HGNC:13797]","synonyms":"KIAA1620","biotype":"protein_coding","ncbi_id":"57716","summary":"This gene encodes a protein involved in peripheral nerve myelin upkeep. The encoded protein contains 2 PDZ domains which were named after PSD95 (post synaptic density protein), DlgA (Drosophila disc large tumor suppressor), and ZO1 (a mammalian tight junction protein). Two alternatively spliced transcript variants have been described for this gene which encode different protein isoforms and which are targeted differently in the Schwann cell. Mutations in this gene cause Charcot-Marie-Tooth neuoropathy, type 4F and Dejerine-Sottas neuropathy. [provided by RefSeq, Jul 2008]","start":40393768,"end":40413366,"strand":-1,"description":"periaxin [Source:HGNC Symbol;Acc:HGNC:13797]"}, {"versioned_ensembl_gene_id":"ENSG00000130957.4","gene_symbol":"FBP2","gene_name":"fructose-bisphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8789","summary":"This gene encodes a gluconeogenesis regulatory enzyme which catalyzes the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate and inorganic phosphate. [provided by RefSeq, Jul 2008]","start":94558720,"end":94593793,"strand":-1,"description":"fructose-bisphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:3607]"}, {"versioned_ensembl_gene_id":"ENSG00000178982.9","gene_symbol":"EIF3K","gene_name":"eukaryotic translation initiation factor 3 subunit K [Source:HGNC Symbol;Acc:HGNC:24656]","synonyms":"PTD001,PRO1474,PLAC-24,M9,HSPC029,EIF3S12,eIF3k,ARG134","biotype":"protein_coding","ncbi_id":"27335","summary":"The 700-kD eukaryotic translation initiation factor-3 (eIF3) is the largest eIF and contains at least 12 subunits, including EIF2S12. eIF3 plays an essential role in translation by binding directly to the 40S ribosomal subunit and promoting formation of the 40S preinitiation complex (Mayeur et al., 2003 [PubMed 14519125]).[supplied by OMIM, Mar 2008]","start":38619082,"end":38636955,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit K [Source:HGNC Symbol;Acc:HGNC:24656]"}, {"versioned_ensembl_gene_id":"ENSG00000009830.11","gene_symbol":"POMT2","gene_name":"protein O-mannosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:19743]","synonyms":"LGMD2N","biotype":"protein_coding","ncbi_id":"29954","summary":"The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS).[provided by RefSeq, Oct 2008]","start":77274956,"end":77320884,"strand":-1,"description":"protein O-mannosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:19743]"}, {"versioned_ensembl_gene_id":"ENSG00000236115.1","gene_symbol":"AL136097.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92205356,"end":92210158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188324.4","gene_symbol":"OR6C6","gene_name":"olfactory receptor family 6 subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:31293]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283365","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55293988,"end":55296569,"strand":-1,"description":"olfactory receptor family 6 subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:31293]"}, {"versioned_ensembl_gene_id":"ENSG00000006015.17","gene_symbol":"C19orf60","gene_name":"chromosome 19 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:26098]","synonyms":"FLJ37391,FLJ34606,FLJ30108,FLJ20850","biotype":"protein_coding","ncbi_id":"55049","summary":null,"start":18588685,"end":18592336,"strand":1,"description":"chromosome 19 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:26098]"}, {"versioned_ensembl_gene_id":"ENSG00000248229.1","gene_symbol":"AC106872.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164987265,"end":164987787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121578.12","gene_symbol":"B4GALT4","gene_name":"beta-1,4-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:927]","synonyms":"beta4Gal-T4","biotype":"protein_coding","ncbi_id":"8702","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. The enzyme encoded by this gene appears to mainly play a role in glycolipid biosynthesis. Two alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":119211732,"end":119241103,"strand":-1,"description":"beta-1,4-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:927]"}, {"versioned_ensembl_gene_id":"ENSG00000137414.5","gene_symbol":"FAM8A1","gene_name":"family with sequence similarity 8 member A1 [Source:HGNC Symbol;Acc:HGNC:16372]","synonyms":"AHCP","biotype":"protein_coding","ncbi_id":"51439","summary":null,"start":17600355,"end":17611719,"strand":1,"description":"family with sequence similarity 8 member A1 [Source:HGNC Symbol;Acc:HGNC:16372]"}, {"versioned_ensembl_gene_id":"ENSG00000279254.1","gene_symbol":"AC020604.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46668870,"end":46670778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115694.14","gene_symbol":"STK25","gene_name":"serine/threonine kinase 25 [Source:HGNC Symbol;Acc:HGNC:11404]","synonyms":"YSK1,SOK1","biotype":"protein_coding","ncbi_id":"10494","summary":"This gene encodes a member of the germinal centre kinase III (GCK III) subfamily of the sterile 20 superfamily of kinases. The encoded enzyme plays a role in serine-threonine liver kinase B1 (LKB1) signaling pathway to regulate neuronal polarization and morphology of the Golgi apparatus. The protein is translocated from the Golgi apparatus to the nucleus in response to chemical anoxia and plays a role in regulation of cell death. A pseudogene associated with this gene is located on chromosome 18. Multiple alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2012]","start":241492674,"end":241509730,"strand":-1,"description":"serine/threonine kinase 25 [Source:HGNC Symbol;Acc:HGNC:11404]"}, {"versioned_ensembl_gene_id":"ENSG00000198457.13","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"P450c21B,CPS1,CYP21B,CAH1,CYP21,CA21H","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32030953,"end":32034322,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000184005.10","gene_symbol":"ST6GALNAC3","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:19343]","synonyms":"SIAT7C","biotype":"protein_coding","ncbi_id":"256435","summary":"ST6GALNAC3 belongs to a family of sialyltransferases that transfer sialic acids from CMP-sialic acid to terminal positions of carbohydrate groups in glycoproteins and glycolipids (Lee et al., 1999 [PubMed 10207017]).[supplied by OMIM, Mar 2008]","start":76074719,"end":76634601,"strand":1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:19343]"}, {"versioned_ensembl_gene_id":"ENSG00000259779.1","gene_symbol":"LINC01922","gene_name":"long intergenic non-protein coding RNA 1922 [Source:HGNC Symbol;Acc:HGNC:52741]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927606","summary":null,"start":74409415,"end":74413209,"strand":1,"description":"long intergenic non-protein coding RNA 1922 [Source:HGNC Symbol;Acc:HGNC:52741]"}, {"versioned_ensembl_gene_id":"ENSG00000148803.11","gene_symbol":"FUOM","gene_name":"fucose mutarotase [Source:HGNC Symbol;Acc:HGNC:24733]","synonyms":"FucU,FucM,FLJ26016,C10orf125","biotype":"protein_coding","ncbi_id":"282969","summary":null,"start":133355154,"end":133358035,"strand":-1,"description":"fucose mutarotase [Source:HGNC Symbol;Acc:HGNC:24733]"}, {"versioned_ensembl_gene_id":"ENSG00000270424.1","gene_symbol":"AC145285.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28749959,"end":28750595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134243.11","gene_symbol":"SORT1","gene_name":"sortilin 1 [Source:HGNC Symbol;Acc:HGNC:11186]","synonyms":"NT3,Gp95","biotype":"protein_coding","ncbi_id":"6272","summary":"This gene encodes a member of the VPS10-related sortilin family of proteins. The encoded preproprotein is proteolytically processed by furin to generate the mature receptor. This receptor plays a role in the trafficking of different proteins to either the cell surface, or subcellular compartments such as lysosomes and endosomes. Expression levels of this gene may influence the risk of myocardial infarction in human patients. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":109309568,"end":109397951,"strand":-1,"description":"sortilin 1 [Source:HGNC Symbol;Acc:HGNC:11186]"}, {"versioned_ensembl_gene_id":"ENSG00000156675.15","gene_symbol":"RAB11FIP1","gene_name":"RAB11 family interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30265]","synonyms":"RCP,Rab11-FIP1,FLJ22622,FLJ22524","biotype":"protein_coding","ncbi_id":"80223","summary":"This gene encodes one of the Rab11-family interacting proteins (Rab11-FIPs), which play a role in the Rab-11 mediated recycling of vesicles. The encoded protein may be involved in endocytic sorting, trafficking of proteins including integrin subunits and epidermal growth factor receptor (EGFR), and transport between the recycling endosome and the trans-Golgi network. Alternative splicing results in multiple transcript variants. A pseudogene is described on the X chromosome. [provided by RefSeq, Dec 2013]","start":37858618,"end":37899467,"strand":-1,"description":"RAB11 family interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30265]"}, {"versioned_ensembl_gene_id":"ENSG00000076382.16","gene_symbol":"SPAG5","gene_name":"sperm associated antigen 5 [Source:HGNC Symbol;Acc:HGNC:13452]","synonyms":"MAP126,hMAP126,DEEPEST","biotype":"protein_coding","ncbi_id":"10615","summary":"This gene encodes a protein associated with the mitotic spindle apparatus. The encoded protein may be involved in the functional and dynamic regulation of mitotic spindles. [provided by RefSeq, Jul 2008]","start":28577565,"end":28599279,"strand":-1,"description":"sperm associated antigen 5 [Source:HGNC Symbol;Acc:HGNC:13452]"}, {"versioned_ensembl_gene_id":"ENSG00000132635.16","gene_symbol":"PCED1A","gene_name":"PC-esterase domain containing 1A [Source:HGNC Symbol;Acc:HGNC:16212]","synonyms":"C20orf81,bA12M19.1,FLJ22376,FAM113A","biotype":"protein_coding","ncbi_id":"64773","summary":"The protein encoded by this gene is a member of the GDSL/SGNH superfamily. Members of this family are hydrolytic enzymes with esterase and lipase activity and broad substrate specificity. This protein belongs to the Pmr5-Cas1p-esterase subfamily in that it contains the catalytic triad comprised of serine, aspartate and histidine and lacks two conserved regions (glycine after strand S2 and GxND motif). A pseudogene of this gene has been identified on the long arm of chromosome 2. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Sep 2012]","start":2835314,"end":2841190,"strand":-1,"description":"PC-esterase domain containing 1A [Source:HGNC Symbol;Acc:HGNC:16212]"}, {"versioned_ensembl_gene_id":"ENSG00000206297.7","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32773904,"end":32782673,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000239830.1","gene_symbol":"RPS4XP22","gene_name":"ribosomal protein S4X pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36125]","synonyms":"RPS4P22","biotype":"processed_pseudogene","ncbi_id":"100131614","summary":null,"start":9683294,"end":9684073,"strand":-1,"description":"ribosomal protein S4X pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36125]"}, {"versioned_ensembl_gene_id":"ENSG00000187257.15","gene_symbol":"RSBN1L","gene_name":"round spermatid basic protein 1 like [Source:HGNC Symbol;Acc:HGNC:24765]","synonyms":"MGC71764,FLJ45813,FLJ42526","biotype":"protein_coding","ncbi_id":"222194","summary":null,"start":77696443,"end":77783022,"strand":1,"description":"round spermatid basic protein 1 like [Source:HGNC Symbol;Acc:HGNC:24765]"}, {"versioned_ensembl_gene_id":"ENSG00000248764.1","gene_symbol":"AC092435.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146934001,"end":146945471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136315.4","gene_symbol":"AL355922.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20919361,"end":20920299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258918.1","gene_symbol":"AL355922.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20897985,"end":20936255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225511.6","gene_symbol":"LINC00475","gene_name":"long intergenic non-protein coding RNA 475 [Source:HGNC Symbol;Acc:HGNC:23569]","synonyms":"C9orf44","biotype":"lincRNA","ncbi_id":"158314","summary":null,"start":92141298,"end":92160114,"strand":1,"description":"long intergenic non-protein coding RNA 475 [Source:HGNC Symbol;Acc:HGNC:23569]"}, {"versioned_ensembl_gene_id":"ENSG00000166963.12","gene_symbol":"MAP1A","gene_name":"microtubule associated protein 1A [Source:HGNC Symbol;Acc:HGNC:6835]","synonyms":"MAP1L","biotype":"protein_coding","ncbi_id":"4130","summary":"This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The product of this gene is a precursor polypeptide that presumably undergoes proteolytic processing to generate the final MAP1A heavy chain and LC2 light chain. Expression of this gene is almost exclusively in the brain. Studies of the rat microtubule-associated protein 1A gene suggested a role in early events of spinal cord development. [provided by RefSeq, Jul 2008]","start":43510958,"end":43531620,"strand":1,"description":"microtubule associated protein 1A [Source:HGNC Symbol;Acc:HGNC:6835]"}, {"versioned_ensembl_gene_id":"ENSG00000280506.1","gene_symbol":"AC233280.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186090.10","gene_symbol":"HTR3D","gene_name":"5-hydroxytryptamine receptor 3D [Source:HGNC Symbol;Acc:HGNC:24004]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200909","summary":"The protein encoded this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit D of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a mitogen and a hormone. This hormone has been linked to neuropsychiatric disorders, including anxiety, depression, and migraine. Serotonin receptors causes fast and depolarizing responses in neurons following activation. The genes encoding subunits C, D and E of this type 3 receptor form a cluster on chromosome 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009]","start":184031544,"end":184039369,"strand":1,"description":"5-hydroxytryptamine receptor 3D [Source:HGNC Symbol;Acc:HGNC:24004]"}, {"versioned_ensembl_gene_id":"ENSG00000235787.1","gene_symbol":"AC092047.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42469640,"end":42469879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224642.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28986195,"end":28987476,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000224662.2","gene_symbol":"ATP6V1G1P3","gene_name":"ATPase H+ transporting V1 subunit G1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37670]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462838","summary":null,"start":136779939,"end":136780218,"strand":1,"description":"ATPase H+ transporting V1 subunit G1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37670]"}, {"versioned_ensembl_gene_id":"ENSG00000166278.14","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31897785,"end":31945672,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000245864.2","gene_symbol":"MEF2C-AS2","gene_name":"MEF2C antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53115]","synonyms":"CTC-467M3.1","biotype":"antisense_RNA","ncbi_id":"109729137","summary":null,"start":88676218,"end":88722831,"strand":1,"description":"MEF2C antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:53115]"}, {"versioned_ensembl_gene_id":"ENSG00000070759.16","gene_symbol":"TESK2","gene_name":"testis-specific kinase 2 [Source:HGNC Symbol;Acc:HGNC:11732]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10420","summary":"This gene product is a serine/threonine protein kinase that contains an N-terminal protein kinase domain that is structurally similar to the kinase domains of testis-specific protein kinase-1 and the LIM motif-containing protein kinases (LIMKs). Its overall structure is most related to the former, indicating that it belongs to the TESK subgroup of the LIMK/TESK family of protein kinases. This gene is predominantly expressed in testis and prostate. The developmental expression pattern of the rat gene in testis suggests an important role for this gene in meitoic stages and/or early stages of spermiogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":45343883,"end":45491166,"strand":-1,"description":"testis-specific kinase 2 [Source:HGNC Symbol;Acc:HGNC:11732]"}, {"versioned_ensembl_gene_id":"ENSG00000267178.3","gene_symbol":"PHF5CP","gene_name":"PHD finger protein 5C pseudogene [Source:HGNC Symbol;Acc:HGNC:32385]","synonyms":"PHF5AP1","biotype":"processed_pseudogene","ncbi_id":"450232","summary":null,"start":19588091,"end":19588415,"strand":-1,"description":"PHD finger protein 5C pseudogene [Source:HGNC Symbol;Acc:HGNC:32385]"}, {"versioned_ensembl_gene_id":"ENSG00000276900.1","gene_symbol":"AC023157.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31729117,"end":31731204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184789.6","gene_symbol":"OR4C10P","gene_name":"olfactory receptor family 4 subfamily C member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:14800]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79526","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48432217,"end":48433147,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:14800]"}, {"versioned_ensembl_gene_id":"ENSG00000112851.14","gene_symbol":"ERBIN","gene_name":"erbb2 interacting protein [Source:HGNC Symbol;Acc:HGNC:15842]","synonyms":"LAP2,ERBB2IP","biotype":"protein_coding","ncbi_id":"55914","summary":"This gene is a member of the leucine-rich repeat and PDZ domain (LAP) family. The encoded protein contains 17 leucine-rich repeats and one PDZ domain. It binds to the unphosphorylated form of the ERBB2 protein and regulates ERBB2 function and localization. It has also been shown to affect the Ras signaling pathway by disrupting Ras-Raf interaction. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":65926475,"end":66082549,"strand":1,"description":"erbb2 interacting protein [Source:HGNC Symbol;Acc:HGNC:15842]"}, {"versioned_ensembl_gene_id":"ENSG00000214961.2","gene_symbol":"FO393409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134272287,"end":134273658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233583.1","gene_symbol":"AL356273.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185262286,"end":185264356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273494.3","gene_symbol":"PANK4","gene_name":"pantothenate kinase 4 [Source:HGNC Symbol;Acc:HGNC:19366]","synonyms":"FLJ10782","biotype":"protein_coding","ncbi_id":"55229","summary":"This gene encodes a protein belonging to the pantothenate kinase family. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by CoA. This family member is most abundant in muscle but is expressed in all tissues. [provided by RefSeq, Jul 2008]","start":2508533,"end":2526600,"strand":-1,"description":"pantothenate kinase 4 [Source:HGNC Symbol;Acc:HGNC:19366]"}, {"versioned_ensembl_gene_id":"ENSG00000241886.1","gene_symbol":"AC112496.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30698207,"end":30721932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225317.3","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31509763,"end":31510574,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000261736.1","gene_symbol":"AC002551.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27643199,"end":27644663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120254.15","gene_symbol":"MTHFD1L","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like [Source:HGNC Symbol;Acc:HGNC:21055]","synonyms":"FTHFSDC1,FLJ21145,DKFZP586G1517","biotype":"protein_coding","ncbi_id":"25902","summary":"The protein encoded by this gene is involved in the synthesis of tetrahydrofolate (THF) in the mitochondrion. THF is important in the de novo synthesis of purines and thymidylate and in the regeneration of methionine from homocysteine. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2011]","start":150865549,"end":151101887,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like [Source:HGNC Symbol;Acc:HGNC:21055]"}, {"versioned_ensembl_gene_id":"ENSG00000261329.5","gene_symbol":"AC016597.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27678940,"end":27718806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198546.14","gene_symbol":"ZNF511","gene_name":"zinc finger protein 511 [Source:HGNC Symbol;Acc:HGNC:28445]","synonyms":"MGC30006","biotype":"protein_coding","ncbi_id":"118472","summary":null,"start":133308475,"end":133313162,"strand":1,"description":"zinc finger protein 511 [Source:HGNC Symbol;Acc:HGNC:28445]"}, {"versioned_ensembl_gene_id":"ENSG00000169026.12","gene_symbol":"MFSD7","gene_name":"major facilitator superfamily domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26177]","synonyms":"LP2561,FLJ22269","biotype":"protein_coding","ncbi_id":"84179","summary":null,"start":681829,"end":689441,"strand":-1,"description":"major facilitator superfamily domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26177]"}, {"versioned_ensembl_gene_id":"ENSG00000145850.8","gene_symbol":"TIMD4","gene_name":"T-cell immunoglobulin and mucin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25132]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91937","summary":null,"start":156919282,"end":156963255,"strand":-1,"description":"T-cell immunoglobulin and mucin domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25132]"}, {"versioned_ensembl_gene_id":"ENSG00000235034.6","gene_symbol":"C19orf81","gene_name":"chromosome 19 open reading frame 81 [Source:HGNC Symbol;Acc:HGNC:40041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342918","summary":null,"start":50649445,"end":50659310,"strand":1,"description":"chromosome 19 open reading frame 81 [Source:HGNC Symbol;Acc:HGNC:40041]"}, {"versioned_ensembl_gene_id":"ENSG00000270560.1","gene_symbol":"APOOP1","gene_name":"apolipoprotein O pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100286948","summary":null,"start":156924119,"end":156924710,"strand":1,"description":"apolipoprotein O pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48739]"}, {"versioned_ensembl_gene_id":"ENSG00000270664.1","gene_symbol":"AC010900.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202995194,"end":202995403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144674.16","gene_symbol":"GOLGA4","gene_name":"golgin A4 [Source:HGNC Symbol;Acc:HGNC:4427]","synonyms":"p230,golgin-240,GOLG,GCP2","biotype":"protein_coding","ncbi_id":"2803","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This protein has been postulated to play a role in Rab6-regulated membrane-tethering events in the Golgi apparatus. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]","start":37243177,"end":37366751,"strand":1,"description":"golgin A4 [Source:HGNC Symbol;Acc:HGNC:4427]"}, {"versioned_ensembl_gene_id":"ENSG00000007216.14","gene_symbol":"SLC13A2","gene_name":"solute carrier family 13 member 2 [Source:HGNC Symbol;Acc:HGNC:10917]","synonyms":"NaDC-1","biotype":"protein_coding","ncbi_id":"9058","summary":"The protein encoded by this gene is a sodium-coupled citrate transporter that is regulated by the chaperone activity of cyclophilin b. The encoded protein may play a role in the formation of kidney stones. [provided by RefSeq, Oct 2016]","start":28473293,"end":28497781,"strand":1,"description":"solute carrier family 13 member 2 [Source:HGNC Symbol;Acc:HGNC:10917]"}, {"versioned_ensembl_gene_id":"ENSG00000231689.2","gene_symbol":"LINC01090","gene_name":"long intergenic non-protein coding RNA 1090 [Source:HGNC Symbol;Acc:HGNC:49201]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355152","summary":null,"start":187712816,"end":188384313,"strand":-1,"description":"long intergenic non-protein coding RNA 1090 [Source:HGNC Symbol;Acc:HGNC:49201]"}, {"versioned_ensembl_gene_id":"ENSG00000155622.6","gene_symbol":"XAGE2","gene_name":"X antigen family member 2 [Source:HGNC Symbol;Acc:HGNC:4112]","synonyms":"XAGE2B,XAGE-2,GAGED3,CT12.2","biotype":"protein_coding","ncbi_id":"9502","summary":"This gene is a member of the XAGE subfamily, which belongs to the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. This gene is strongly expressed in normal testis, and in Ewing's sarcoma, rhabdomyosarcoma, a breast cancer and a germ cell tumor. The protein encoded by this gene shares a sequence similarity with other GAGE/PAGE proteins. Because of the expression pattern and the sequence similarity, this protein also belongs to a family of CT (cancer-testis) antigens. [provided by RefSeq, Jul 2008]","start":52369030,"end":52375680,"strand":1,"description":"X antigen family member 2 [Source:HGNC Symbol;Acc:HGNC:4112]"}, {"versioned_ensembl_gene_id":"ENSG00000179028.4","gene_symbol":"AC245177.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52199840,"end":52203235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134970.13","gene_symbol":"TMED7","gene_name":"transmembrane p24 trafficking protein 7 [Source:HGNC Symbol;Acc:HGNC:24253]","synonyms":"p24gamma3,p24g3,FLJ90481,CGI-109","biotype":"protein_coding","ncbi_id":"51014","summary":null,"start":115613508,"end":115632992,"strand":-1,"description":"transmembrane p24 trafficking protein 7 [Source:HGNC Symbol;Acc:HGNC:24253]"}, {"versioned_ensembl_gene_id":"ENSG00000254515.1","gene_symbol":"AP001124.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121238304,"end":121238688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257350.1","gene_symbol":"AC027287.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55122668,"end":55124120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260345.1","gene_symbol":"AC009052.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":57461055,"end":57462737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206489.9","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"PNUTS,CAT53,p99,FB19","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30589896,"end":30608107,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000148153.13","gene_symbol":"INIP","gene_name":"INTS3 and NABP interacting protein [Source:HGNC Symbol;Acc:HGNC:24994]","synonyms":"hSSBIP1,HSPC043,C9orf80,SOSS-C,MISE","biotype":"protein_coding","ncbi_id":"58493","summary":"The protein encoded by this gene is a subunit of single-stranded DNA binding complexes that are important for maintaining genome stability. These complexes are involved in G2/M checkpoint control and homologous recombination repair. [provided by RefSeq, Jul 2016]","start":112683926,"end":112718236,"strand":-1,"description":"INTS3 and NABP interacting protein [Source:HGNC Symbol;Acc:HGNC:24994]"}, {"versioned_ensembl_gene_id":"ENSG00000253216.1","gene_symbol":"AC022790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69446057,"end":69446260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224778.1","gene_symbol":"CENPIP1","gene_name":"centromere protein I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39575]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419337","summary":null,"start":19126399,"end":19139611,"strand":1,"description":"centromere protein I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39575]"}, {"versioned_ensembl_gene_id":"ENSG00000165828.14","gene_symbol":"PRAP1","gene_name":"proline rich acidic protein 1 [Source:HGNC Symbol;Acc:HGNC:23304]","synonyms":"UPA","biotype":"protein_coding","ncbi_id":"118471","summary":null,"start":133347146,"end":133352683,"strand":1,"description":"proline rich acidic protein 1 [Source:HGNC Symbol;Acc:HGNC:23304]"}, {"versioned_ensembl_gene_id":"ENSG00000225935.1","gene_symbol":"BANF1P5","gene_name":"barrier to autointegration factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43885]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101290503","summary":null,"start":107642765,"end":107643023,"strand":-1,"description":"barrier to autointegration factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43885]"}, {"versioned_ensembl_gene_id":"ENSG00000267620.1","gene_symbol":"AC090771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60196555,"end":60198172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175376.8","gene_symbol":"EIF1AD","gene_name":"eukaryotic translation initiation factor 1A domain containing [Source:HGNC Symbol;Acc:HGNC:28147]","synonyms":"MGC11102,haponin","biotype":"protein_coding","ncbi_id":"84285","summary":null,"start":65996545,"end":66002176,"strand":-1,"description":"eukaryotic translation initiation factor 1A domain containing [Source:HGNC Symbol;Acc:HGNC:28147]"}, {"versioned_ensembl_gene_id":"ENSG00000235701.1","gene_symbol":"PCBP2P1","gene_name":"poly(rC) binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060045","summary":null,"start":39171130,"end":39172106,"strand":-1,"description":"poly(rC) binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8649]"}, {"versioned_ensembl_gene_id":"ENSG00000250076.1","gene_symbol":"AC017013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33010948,"end":33011746,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145075.11","gene_symbol":"CCDC39","gene_name":"coiled-coil domain containing 39 [Source:HGNC Symbol;Acc:HGNC:25244]","synonyms":"DKFZp434A128,CILD14,FAP59","biotype":"protein_coding","ncbi_id":"339829","summary":"The protein encoded by this gene is involved in the motility of cilia and flagella. The encoded protein is essential for the assembly of dynein regulatory and inner dynein arm complexes, which regulate ciliary beat. Defects in this gene are a cause of primary ciliary dyskinesia type 14 (CILD14). [provided by RefSeq, Jul 2011]","start":180602858,"end":180871005,"strand":-1,"description":"coiled-coil domain containing 39 [Source:HGNC Symbol;Acc:HGNC:25244]"}, {"versioned_ensembl_gene_id":"ENSG00000244395.6","gene_symbol":"RBMY1D","gene_name":"RNA binding motif protein, Y-linked, family 1, member D [Source:HGNC Symbol;Acc:HGNC:23915]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378949","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein likely functions as a splicing factor during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":21880076,"end":21894526,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 1, member D [Source:HGNC Symbol;Acc:HGNC:23915]"}, {"versioned_ensembl_gene_id":"ENSG00000232541.10","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"DFNB53,DFNA13,HKE5","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33302792,"end":33329578,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000249882.1","gene_symbol":"LINC02501","gene_name":"long intergenic non-protein coding RNA 2501 [Source:HGNC Symbol;Acc:HGNC:53489]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374565","summary":null,"start":31506666,"end":31558821,"strand":1,"description":"long intergenic non-protein coding RNA 2501 [Source:HGNC Symbol;Acc:HGNC:53489]"}, {"versioned_ensembl_gene_id":"ENSG00000153113.23","gene_symbol":"CAST","gene_name":"calpastatin [Source:HGNC Symbol;Acc:HGNC:1515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"831","summary":"The protein encoded by this gene is an endogenous calpain (calcium-dependent cysteine protease) inhibitor. It consists of an N-terminal domain L and four repetitive calpain-inhibition domains (domains 1-4), and it is involved in the proteolysis of amyloid precursor protein. The calpain/calpastatin system is involved in numerous membrane fusion events, such as neural vesicle exocytosis and platelet and red-cell aggregation. The encoded protein is also thought to affect the expression levels of genes encoding structural or regulatory proteins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2010]","start":96525267,"end":96779595,"strand":1,"description":"calpastatin [Source:HGNC Symbol;Acc:HGNC:1515]"}, {"versioned_ensembl_gene_id":"ENSG00000248340.2","gene_symbol":"AC106047.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26873561,"end":26874349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168291.12","gene_symbol":"PDHB","gene_name":"pyruvate dehydrogenase (lipoamide) beta [Source:HGNC Symbol;Acc:HGNC:8808]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5162","summary":"The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and carbon dioxide, and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 beta subunit. Mutations in this gene are associated with pyruvate dehydrogenase E1-beta deficiency. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2012]","start":58427630,"end":58433857,"strand":-1,"description":"pyruvate dehydrogenase (lipoamide) beta [Source:HGNC Symbol;Acc:HGNC:8808]"}, {"versioned_ensembl_gene_id":"ENSG00000121774.17","gene_symbol":"KHDRBS1","gene_name":"KH RNA binding domain containing, signal transduction associated 1 [Source:HGNC Symbol;Acc:HGNC:18116]","synonyms":"FLJ34027,Sam68,p62","biotype":"protein_coding","ncbi_id":"10657","summary":"This gene encodes a member of the K homology domain-containing, RNA-binding, signal transduction-associated protein family. The encoded protein appears to have many functions and may be involved in a variety of cellular processes, including alternative splicing, cell cycle regulation, RNA 3'-end formation, tumorigenesis, and regulation of human immunodeficiency virus gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":32013829,"end":32060850,"strand":1,"description":"KH RNA binding domain containing, signal transduction associated 1 [Source:HGNC Symbol;Acc:HGNC:18116]"}, {"versioned_ensembl_gene_id":"ENSG00000196372.12","gene_symbol":"ASB13","gene_name":"ankyrin repeat and SOCS box containing 13 [Source:HGNC Symbol;Acc:HGNC:19765]","synonyms":"MGC19879,FLJ13134","biotype":"protein_coding","ncbi_id":"79754","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and a SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Multiple alternatively spliced transcript variants, both protein-coding and not protein-coding, have been described for this gene. [provided by RefSeq, Nov 2010]","start":5638867,"end":5666595,"strand":-1,"description":"ankyrin repeat and SOCS box containing 13 [Source:HGNC Symbol;Acc:HGNC:19765]"}, {"versioned_ensembl_gene_id":"ENSG00000186487.17","gene_symbol":"MYT1L","gene_name":"myelin transcription factor 1 like [Source:HGNC Symbol;Acc:HGNC:7623]","synonyms":"ZC2HC4B,ZC2H2C2,NZF1,KIAA1106","biotype":"protein_coding","ncbi_id":"23040","summary":"This gene encodes a member of the zinc finger superfamily of transcription factors whose expression, thus far, has been found only in neuronal tissues. The encoded protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in this gene have been associated with an autosomal dominant form of cognitive disability and with autism spectrum disorder. Alternative splicing results in multiple variants. [provided by RefSeq, Jul 2017]","start":1789113,"end":2331260,"strand":-1,"description":"myelin transcription factor 1 like [Source:HGNC Symbol;Acc:HGNC:7623]"}, {"versioned_ensembl_gene_id":"ENSG00000249359.2","gene_symbol":"AC093274.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21323873,"end":21341375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227449.8","gene_symbol":"FGF7P6","gene_name":"fibroblast growth factor 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:27852]","synonyms":"KGFLP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387628","summary":null,"start":62376161,"end":62435199,"strand":1,"description":"fibroblast growth factor 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:27852]"}, {"versioned_ensembl_gene_id":"ENSG00000198399.14","gene_symbol":"ITSN2","gene_name":"intersectin 2 [Source:HGNC Symbol;Acc:HGNC:6184]","synonyms":"SH3D1B,PRO2015,KIAA1256,SWAP,SWA,SH3P18","biotype":"protein_coding","ncbi_id":"50618","summary":"This gene encodes a cytoplasmic protein which contains SH3 domains. This protein is a member of a family of proteins involved in clathrin-mediated endocytosis. Intersectin 2 is thought to regulate the formation of clathrin-coated vesicles and also may function in the induction of T cell antigen receptor (TCR) endocytosis. [provided by RefSeq, Jan 2017]","start":24202864,"end":24360714,"strand":-1,"description":"intersectin 2 [Source:HGNC Symbol;Acc:HGNC:6184]"}, {"versioned_ensembl_gene_id":"ENSG00000256898.1","gene_symbol":"AP002770.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73921665,"end":73922196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251182.1","gene_symbol":"LINC02497","gene_name":"long intergenic non-protein coding RNA 2497 [Source:HGNC Symbol;Acc:HGNC:53482]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723778","summary":null,"start":31171144,"end":31211675,"strand":1,"description":"long intergenic non-protein coding RNA 2497 [Source:HGNC Symbol;Acc:HGNC:53482]"}, {"versioned_ensembl_gene_id":"ENSG00000231838.1","gene_symbol":"CR769775.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62028426,"end":62076349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259144.2","gene_symbol":"RANBP20P","gene_name":"RAN binding protein 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:19734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326627","summary":null,"start":20720742,"end":20723127,"strand":-1,"description":"RAN binding protein 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:19734]"}, {"versioned_ensembl_gene_id":"ENSG00000224052.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"HTATSF1P,dJ1033B10.6,TAT-SF1-L","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33215710,"end":33217601,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000266767.1","gene_symbol":"AP000897.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7741310,"end":7754831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224608.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31312948,"end":31400264,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000254459.1","gene_symbol":"AP002812.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77829654,"end":77872262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138769.10","gene_symbol":"CDKL2","gene_name":"cyclin dependent kinase like 2 [Source:HGNC Symbol;Acc:HGNC:1782]","synonyms":"P56,KKIAMRE","biotype":"protein_coding","ncbi_id":"8999","summary":"This gene product is a member of a large family of CDC2-related serine/threonine protein kinases. It accumulates primarily in the cytoplasm, with lower levels in the nucleus. [provided by RefSeq, Jul 2008]","start":75578005,"end":75630716,"strand":-1,"description":"cyclin dependent kinase like 2 [Source:HGNC Symbol;Acc:HGNC:1782]"}, {"versioned_ensembl_gene_id":"ENSG00000213115.2","gene_symbol":"AC104131.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188227189,"end":188228382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236187.1","gene_symbol":"GJA6P","gene_name":"gap junction protein alpha 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:32542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100126825","summary":null,"start":18535079,"end":18536120,"strand":1,"description":"gap junction protein alpha 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:32542]"}, {"versioned_ensembl_gene_id":"ENSG00000165076.13","gene_symbol":"PRSS37","gene_name":"protease, serine 37 [Source:HGNC Symbol;Acc:HGNC:29211]","synonyms":null,"biotype":"protein_coding","ncbi_id":"136242","summary":null,"start":141836286,"end":141841487,"strand":-1,"description":"protease, serine 37 [Source:HGNC Symbol;Acc:HGNC:29211]"}, {"versioned_ensembl_gene_id":"ENSG00000005381.7","gene_symbol":"MPO","gene_name":"myeloperoxidase [Source:HGNC Symbol;Acc:HGNC:7218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4353","summary":"Myeloperoxidase (MPO) is a heme protein synthesized during myeloid differentiation that constitutes the major component of neutrophil azurophilic granules. Produced as a single chain precursor, myeloperoxidase is subsequently cleaved into a light and heavy chain. The mature myeloperoxidase is a tetramer composed of 2 light chains and 2 heavy chains. This enzyme produces hypohalous acids central to the microbicidal activity of neutrophils. [provided by RefSeq, Nov 2014]","start":58269856,"end":58280935,"strand":-1,"description":"myeloperoxidase [Source:HGNC Symbol;Acc:HGNC:7218]"}, {"versioned_ensembl_gene_id":"ENSG00000181163.13","gene_symbol":"NPM1","gene_name":"nucleophosmin [Source:HGNC Symbol;Acc:HGNC:7910]","synonyms":"B23,NPM","biotype":"protein_coding","ncbi_id":"4869","summary":"The protein encoded by this gene is involved in several cellular processes, including centrosome duplication, protein chaperoning, and cell proliferation. The encoded phosphoprotein shuttles between the nucleolus, nucleus, and cytoplasm, chaperoning ribosomal proteins and core histones from the nucleus to the cytoplasm. This protein is also known to sequester the tumor suppressor ARF in the nucleolus, protecting it from degradation until it is needed. Mutations in this gene are associated with acute myeloid leukemia. Dozens of pseudogenes of this gene have been identified. [provided by RefSeq, Aug 2017]","start":171387116,"end":171411137,"strand":1,"description":"nucleophosmin [Source:HGNC Symbol;Acc:HGNC:7910]"}, {"versioned_ensembl_gene_id":"ENSG00000186205.12","gene_symbol":"MARC1","gene_name":"mitochondrial amidoxime reducing component 1 [Source:HGNC Symbol;Acc:HGNC:26189]","synonyms":"MOSC1,FLJ22390","biotype":"protein_coding","ncbi_id":"64757","summary":null,"start":220786759,"end":220819657,"strand":1,"description":"mitochondrial amidoxime reducing component 1 [Source:HGNC Symbol;Acc:HGNC:26189]"}, {"versioned_ensembl_gene_id":"ENSG00000249082.2","gene_symbol":"C5orf66-AS1","gene_name":"C5orf66 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49679]","synonyms":"CTC-276P9.1,Epist","biotype":"lincRNA","ncbi_id":"101927953","summary":null,"start":135038831,"end":135040047,"strand":-1,"description":"C5orf66 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49679]"}, {"versioned_ensembl_gene_id":"ENSG00000266576.1","gene_symbol":"MARK2P14","gene_name":"microtubule affinity regulating kinase 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44495]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631261","summary":null,"start":11908448,"end":11914234,"strand":1,"description":"microtubule affinity regulating kinase 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44495]"}, {"versioned_ensembl_gene_id":"ENSG00000072518.20","gene_symbol":"MARK2","gene_name":"microtubule affinity regulating kinase 2 [Source:HGNC Symbol;Acc:HGNC:3332]","synonyms":"Par1b,PAR-1B,PAR-1,EMK1","biotype":"protein_coding","ncbi_id":"2011","summary":"This gene encodes a member of the Par-1 family of serine/threonine protein kinases. The protein is an important regulator of cell polarity in epithelial and neuronal cells, and also controls the stability of microtubules through phosphorylation and inactivation of several microtubule-associating proteins. The protein localizes to cell membranes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009]","start":63838928,"end":63911019,"strand":1,"description":"microtubule affinity regulating kinase 2 [Source:HGNC Symbol;Acc:HGNC:3332]"}, {"versioned_ensembl_gene_id":"ENSG00000273084.1","gene_symbol":"AC092171.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5428731,"end":5429672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217289.3","gene_symbol":"AC079776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129992889,"end":129994040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169379.15","gene_symbol":"ARL13B","gene_name":"ADP ribosylation factor like GTPase 13B [Source:HGNC Symbol;Acc:HGNC:25419]","synonyms":"JBTS8,DKFZp761H079,ARL2L1","biotype":"protein_coding","ncbi_id":"200894","summary":"This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":93980139,"end":94055668,"strand":1,"description":"ADP ribosylation factor like GTPase 13B [Source:HGNC Symbol;Acc:HGNC:25419]"}, {"versioned_ensembl_gene_id":"ENSG00000169994.18","gene_symbol":"MYO7B","gene_name":"myosin VIIB [Source:HGNC Symbol;Acc:HGNC:7607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4648","summary":"The protein encoded by this gene is found in brush border microvilli of epithelial cells in the intestines and kidneys. The encoded protein is involved in linking protocadherins to the actin cytoskeleton and is essential for proper microvilli function. This protein aids in the accumulation of intermicrovillar adhesion components such as harmonin and ANKS4B, and this accumulation is necessary for normal brush border action. [provided by RefSeq, Jan 2017]","start":127535802,"end":127637729,"strand":1,"description":"myosin VIIB [Source:HGNC Symbol;Acc:HGNC:7607]"}, {"versioned_ensembl_gene_id":"ENSG00000092871.16","gene_symbol":"RFFL","gene_name":"ring finger and FYVE like domain containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:24821]","synonyms":"CARP-2,RNF34L,RNF189,rififylin,fring,CARP2","biotype":"protein_coding","ncbi_id":"117584","summary":null,"start":35005990,"end":35089319,"strand":-1,"description":"ring finger and FYVE like domain containing E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:24821]"}, {"versioned_ensembl_gene_id":"ENSG00000257703.5","gene_symbol":"AC068643.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103080950,"end":103178675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228329.1","gene_symbol":"LINC01890","gene_name":"long intergenic non-protein coding RNA 1890 [Source:HGNC Symbol;Acc:HGNC:52709]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374791","summary":null,"start":68832816,"end":68837192,"strand":-1,"description":"long intergenic non-protein coding RNA 1890 [Source:HGNC Symbol;Acc:HGNC:52709]"}, {"versioned_ensembl_gene_id":"ENSG00000276072.2","gene_symbol":"AATF","gene_name":"apoptosis antagonizing transcription factor [Source:HGNC Symbol;Acc:HGNC:19235]","synonyms":"BFR2,DED,CHE1,CHE-1","biotype":"protein_coding","ncbi_id":"26574","summary":"The protein encoded by this gene was identified on the basis of its interaction with MAP3K12/DLK, a protein kinase known to be involved in the induction of cell apoptosis. This gene product contains a leucine zipper, which is a characteristic motif of transcription factors, and was shown to exhibit strong transactivation activity when fused to Gal4 DNA binding domain. Overexpression of this gene interfered with MAP3K12 induced apoptosis. [provided by RefSeq, Jul 2008]","start":36950708,"end":37058704,"strand":1,"description":"apoptosis antagonizing transcription factor [Source:HGNC Symbol;Acc:HGNC:19235]"}, {"versioned_ensembl_gene_id":"ENSG00000140577.15","gene_symbol":"CRTC3","gene_name":"CREB regulated transcription coactivator 3 [Source:HGNC Symbol;Acc:HGNC:26148]","synonyms":"FLJ21868","biotype":"protein_coding","ncbi_id":"64784","summary":"This gene is a member of the CREB regulated transcription coactivator gene family. This family regulates CREB-dependent gene transcription in a phosphorylation-independent manner and may be selective for cAMP-responsive genes. The protein encoded by this gene may induce mitochondrial biogenesis and attenuate catecholamine signaling in adipose tissue. A translocation event between this gene and Notch coactivator mastermind-like gene 2, which results in a fusion protein, has been reported in mucoepidermoid carcinomas. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":90529925,"end":90645345,"strand":1,"description":"CREB regulated transcription coactivator 3 [Source:HGNC Symbol;Acc:HGNC:26148]"}, {"versioned_ensembl_gene_id":"ENSG00000249156.2","gene_symbol":"AC233724.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17610496,"end":17611583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180475.4","gene_symbol":"OR10Q1","gene_name":"olfactory receptor family 10 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:15134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219960","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58227882,"end":58228918,"strand":-1,"description":"olfactory receptor family 10 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:15134]"}, {"versioned_ensembl_gene_id":"ENSG00000198074.9","gene_symbol":"AKR1B10","gene_name":"aldo-keto reductase family 1 member B10 [Source:HGNC Symbol;Acc:HGNC:382]","synonyms":"HSI,HIS,ARL1,ARL-1,ALDRLn,AKR1B12,AKR1B11","biotype":"protein_coding","ncbi_id":"57016","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. This member can efficiently reduce aliphatic and aromatic aldehydes, and it is less active on hexoses. It is highly expressed in adrenal gland, small intestine, and colon, and may play an important role in liver carcinogenesis. [provided by RefSeq, Jul 2008]","start":134527592,"end":134541408,"strand":1,"description":"aldo-keto reductase family 1 member B10 [Source:HGNC Symbol;Acc:HGNC:382]"}, {"versioned_ensembl_gene_id":"ENSG00000277405.2","gene_symbol":"SERPINA6","gene_name":"serpin family A member 6 [Source:HGNC Symbol;Acc:HGNC:1540]","synonyms":"CBG","biotype":"protein_coding","ncbi_id":"866","summary":"This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008]","start":94304248,"end":94323394,"strand":-1,"description":"serpin family A member 6 [Source:HGNC Symbol;Acc:HGNC:1540]"}, {"versioned_ensembl_gene_id":"ENSG00000197887.4","gene_symbol":"OR1S2","gene_name":"olfactory receptor family 1 subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:15141]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219958","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58203202,"end":58204181,"strand":-1,"description":"olfactory receptor family 1 subfamily S member 2 [Source:HGNC Symbol;Acc:HGNC:15141]"}, {"versioned_ensembl_gene_id":"ENSG00000283988.1","gene_symbol":"AC233724.19","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17593798,"end":17594394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185052.11","gene_symbol":"SLC24A3","gene_name":"solute carrier family 24 member 3 [Source:HGNC Symbol;Acc:HGNC:10977]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57419","summary":"Plasma membrane sodium/calcium exchangers are an important component of intracellular calcium homeostasis and electrical conduction. Potassium-dependent sodium/calcium exchangers such as SLC24A3 are believed to transport 1 intracellular calcium and 1 potassium ion in exchange for 4 extracellular sodium ions (Kraev et al., 2001 [PubMed 11294880]).[supplied by OMIM, Mar 2008]","start":19212646,"end":19722937,"strand":1,"description":"solute carrier family 24 member 3 [Source:HGNC Symbol;Acc:HGNC:10977]"}, {"versioned_ensembl_gene_id":"ENSG00000216718.7","gene_symbol":"AL024509.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25261239,"end":25261731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211691.2","gene_symbol":"TRGJP","gene_name":"T-cell receptor gamma joining P [Source:HGNC Symbol;Acc:HGNC:12279]","synonyms":"TCRGJP,JP","biotype":"TR_J_gene","ncbi_id":"6970","summary":null,"start":38273587,"end":38273647,"strand":-1,"description":"T-cell receptor gamma joining P [Source:HGNC Symbol;Acc:HGNC:12279]"}, {"versioned_ensembl_gene_id":"ENSG00000255131.2","gene_symbol":"OR9L1P","gene_name":"olfactory receptor family 9 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14761]","synonyms":"OR9L2P","biotype":"unprocessed_pseudogene","ncbi_id":"79301","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58077348,"end":58078603,"strand":-1,"description":"olfactory receptor family 9 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14761]"}, {"versioned_ensembl_gene_id":"ENSG00000206302.10","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"IDDM1,HLA-DQB,CELIAC1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32587742,"end":32595353,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000172377.2","gene_symbol":"OR9I1","gene_name":"olfactory receptor family 9 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:14718]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219954","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58116742,"end":58125530,"strand":-1,"description":"olfactory receptor family 9 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:14718]"}, {"versioned_ensembl_gene_id":"ENSG00000283117.1","gene_symbol":"MGC4859","gene_name":"uncharacterized LOC79150 [Source:NCBI gene;Acc:79150]","synonyms":null,"biotype":"lincRNA","ncbi_id":"79150","summary":null,"start":10449820,"end":10779944,"strand":-1,"description":"uncharacterized LOC79150 [Source:NCBI gene;Acc:79150]"}, {"versioned_ensembl_gene_id":"ENSG00000237055.1","gene_symbol":"MTCO1P48","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:52113]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075176","summary":null,"start":94899566,"end":94900661,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:52113]"}, {"versioned_ensembl_gene_id":"ENSG00000275799.1","gene_symbol":"AP001059.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44244545,"end":44244993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141194.6","gene_symbol":"OR4D1","gene_name":"olfactory receptor family 4 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:8293]","synonyms":"TPCR16,OR4D3","biotype":"protein_coding","ncbi_id":"26689","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58148449,"end":58159555,"strand":1,"description":"olfactory receptor family 4 subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:8293]"}, {"versioned_ensembl_gene_id":"ENSG00000141738.13","gene_symbol":"GRB7","gene_name":"growth factor receptor bound protein 7 [Source:HGNC Symbol;Acc:HGNC:4567]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2886","summary":"The product of this gene belongs to a small family of adapter proteins that are known to interact with a number of receptor tyrosine kinases and signaling molecules. This gene encodes a growth factor receptor-binding protein that interacts with epidermal growth factor receptor (EGFR) and ephrin receptors. The protein plays a role in the integrin signaling pathway and cell migration by binding with focal adhesion kinase (FAK). Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":39737927,"end":39747291,"strand":1,"description":"growth factor receptor bound protein 7 [Source:HGNC Symbol;Acc:HGNC:4567]"}, {"versioned_ensembl_gene_id":"ENSG00000249236.1","gene_symbol":"AC008892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56059050,"end":56067372,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100300.17","gene_symbol":"TSPO","gene_name":"translocator protein [Source:HGNC Symbol;Acc:HGNC:1158]","synonyms":"IBP,DBI,BZRP,PKBS,pk18,PBR,mDRC,MBR","biotype":"protein_coding","ncbi_id":"706","summary":"Present mainly in the mitochondrial compartment of peripheral tissues, the protein encoded by this gene interacts with some benzodiazepines and has different affinities than its endogenous counterpart. The protein is a key factor in the flow of cholesterol into mitochondria to permit the initiation of steroid hormone synthesis. Alternatively spliced transcript variants have been reported; one of the variants lacks an internal exon and is considered non-coding, and the other variants encode the same protein. [provided by RefSeq, Feb 2012]","start":43151514,"end":43163242,"strand":1,"description":"translocator protein [Source:HGNC Symbol;Acc:HGNC:1158]"}, {"versioned_ensembl_gene_id":"ENSG00000230183.4","gene_symbol":"CNOT6LP1","gene_name":"CCR4-NOT transcription complex subunit 6-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729530","summary":null,"start":56005715,"end":56007176,"strand":-1,"description":"CCR4-NOT transcription complex subunit 6-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32355]"}, {"versioned_ensembl_gene_id":"ENSG00000261789.1","gene_symbol":"AC023830.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4560001,"end":4561662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175928.5","gene_symbol":"LRRN1","gene_name":"leucine rich repeat neuronal 1 [Source:HGNC Symbol;Acc:HGNC:20980]","synonyms":"FIGLER3","biotype":"protein_coding","ncbi_id":"57633","summary":null,"start":3799437,"end":3847703,"strand":1,"description":"leucine rich repeat neuronal 1 [Source:HGNC Symbol;Acc:HGNC:20980]"}, {"versioned_ensembl_gene_id":"ENSG00000273148.1","gene_symbol":"AL035563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18794529,"end":18796067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116141.15","gene_symbol":"MARK1","gene_name":"microtubule affinity regulating kinase 1 [Source:HGNC Symbol;Acc:HGNC:6896]","synonyms":"PAR-1C,MARK","biotype":"protein_coding","ncbi_id":"4139","summary":null,"start":220528183,"end":220664461,"strand":1,"description":"microtubule affinity regulating kinase 1 [Source:HGNC Symbol;Acc:HGNC:6896]"}, {"versioned_ensembl_gene_id":"ENSG00000229486.2","gene_symbol":"AC104454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84015865,"end":84018371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227265.2","gene_symbol":"AL845331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94734655,"end":94735844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197320.5","gene_symbol":"AC060834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9726241,"end":9728272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271077.1","gene_symbol":"AC096553.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9634270,"end":9635703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259089.2","gene_symbol":"GRAMD4P5","gene_name":"GRAM domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49140]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631249","summary":null,"start":20813299,"end":20814958,"strand":1,"description":"GRAM domain containing 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49140]"}, {"versioned_ensembl_gene_id":"ENSG00000274215.1","gene_symbol":"AC106028.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92808451,"end":92809057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266951.2","gene_symbol":"AC093072.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15613247,"end":15614553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186272.12","gene_symbol":"ZNF17","gene_name":"zinc finger protein 17 [Source:HGNC Symbol;Acc:HGNC:12958]","synonyms":"KOX10,KIAA1947,HPF3,FLJ46615,FLJ46058,FLJ40864","biotype":"protein_coding","ncbi_id":"7565","summary":null,"start":57411163,"end":57421939,"strand":1,"description":"zinc finger protein 17 [Source:HGNC Symbol;Acc:HGNC:12958]"}, {"versioned_ensembl_gene_id":"ENSG00000278854.1","gene_symbol":"AC007275.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7845485,"end":7846454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282403.1","gene_symbol":"AC131056.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36343345,"end":36343444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268545.1","gene_symbol":"VN1R107P","gene_name":"vomeronasal 1 receptor 107 pseudogene [Source:HGNC Symbol;Acc:HGNC:37431]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312849","summary":null,"start":57459912,"end":57460120,"strand":1,"description":"vomeronasal 1 receptor 107 pseudogene [Source:HGNC Symbol;Acc:HGNC:37431]"}, {"versioned_ensembl_gene_id":"ENSG00000250816.1","gene_symbol":"DCAF13P2","gene_name":"DDB1 and CUL4 associated factor 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43867]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288979","summary":null,"start":17202274,"end":17203145,"strand":1,"description":"DDB1 and CUL4 associated factor 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43867]"}, {"versioned_ensembl_gene_id":"ENSG00000229393.1","gene_symbol":"AL139246.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2493437,"end":2494479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111653.19","gene_symbol":"ING4","gene_name":"inhibitor of growth family member 4 [Source:HGNC Symbol;Acc:HGNC:19423]","synonyms":"p29ING4,my036","biotype":"protein_coding","ncbi_id":"51147","summary":"This gene encodes a tumor suppressor protein that contains a PHD-finger, which is a common motif in proteins involved in chromatin remodeling. This protein can bind TP53 and EP300/p300, a component of the histone acetyl transferase complex, suggesting its involvement in the TP53-dependent regulatory pathway. Multiple alternatively spliced transcript variants have been observed that encode distinct proteins. [provided by RefSeq, Jul 2008]","start":6650280,"end":6663148,"strand":-1,"description":"inhibitor of growth family member 4 [Source:HGNC Symbol;Acc:HGNC:19423]"}, {"versioned_ensembl_gene_id":"ENSG00000235163.2","gene_symbol":"AC096644.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220448516,"end":220448853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277603.4","gene_symbol":"TPO","gene_name":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]","synonyms":"TPX","biotype":"protein_coding","ncbi_id":"7173","summary":"This gene encodes a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones, thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis, including congenital hypothyroidism, congenital goiter, and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2011]","start":1372594,"end":1540021,"strand":1,"description":"thyroid peroxidase [Source:HGNC Symbol;Acc:HGNC:12015]"}, {"versioned_ensembl_gene_id":"ENSG00000259170.1","gene_symbol":"AC090985.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92470233,"end":92471546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279358.1","gene_symbol":"AP002833.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126934886,"end":126937150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233392.5","gene_symbol":"AC104809.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":240954617,"end":240967451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198237.8","gene_symbol":"AC131392.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69875271,"end":69920867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254607.2","gene_symbol":"AP001783.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126652852,"end":126682104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115488.3","gene_symbol":"NEU2","gene_name":"neuraminidase 2 [Source:HGNC Symbol;Acc:HGNC:7759]","synonyms":"SIAL2","biotype":"protein_coding","ncbi_id":"4759","summary":"This gene belongs to a family of glycohydrolytic enzymes which remove sialic acid residues from glycoproteins and glycolipids. Expression studies in COS7 cells confirmed that this gene encodes a functional sialidase. Its cytosolic localization was demonstrated by cell fractionation experiments. [provided by RefSeq, Jul 2008]","start":233032672,"end":233035057,"strand":1,"description":"neuraminidase 2 [Source:HGNC Symbol;Acc:HGNC:7759]"}, {"versioned_ensembl_gene_id":"ENSG00000017260.19","gene_symbol":"ATP2C1","gene_name":"ATPase secretory pathway Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:13211]","synonyms":"BCPM,ATP2C1A,SPCA1,PMR1,KIAA1347","biotype":"protein_coding","ncbi_id":"27032","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":130850595,"end":131016712,"strand":1,"description":"ATPase secretory pathway Ca2+ transporting 1 [Source:HGNC Symbol;Acc:HGNC:13211]"}, {"versioned_ensembl_gene_id":"ENSG00000107968.9","gene_symbol":"MAP3K8","gene_name":"mitogen-activated protein kinase kinase kinase 8 [Source:HGNC Symbol;Acc:HGNC:6860]","synonyms":"Tpl-2,MEKK8,ESTF,EST,COT,c-COT","biotype":"protein_coding","ncbi_id":"1326","summary":"This gene is an oncogene that encodes a member of the serine/threonine protein kinase family. The encoded protein localizes to the cytoplasm and can activate both the MAP kinase and JNK kinase pathways. This protein was shown to activate IkappaB kinases, and thus induce the nuclear production of NF-kappaB. This protein was also found to promote the production of TNF-alpha and IL-2 during T lymphocyte activation. This gene may also utilize a downstream in-frame translation start codon, and thus produce an isoform containing a shorter N-terminus. The shorter isoform has been shown to display weaker transforming activity. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011]","start":30433937,"end":30461833,"strand":1,"description":"mitogen-activated protein kinase kinase kinase 8 [Source:HGNC Symbol;Acc:HGNC:6860]"}, {"versioned_ensembl_gene_id":"ENSG00000224656.1","gene_symbol":"AL009172.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47718002,"end":47719099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278382.1","gene_symbol":"AL161629.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90108244,"end":90108518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206308.11","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32397298,"end":32402508,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000226206.1","gene_symbol":"BX470209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89799695,"end":89821753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218766.1","gene_symbol":"AL450338.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85868953,"end":85869464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214491.8","gene_symbol":"SEC14L6","gene_name":"SEC14 like lipid binding 6 [Source:HGNC Symbol;Acc:HGNC:40047]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730005","summary":null,"start":30522799,"end":30546682,"strand":-1,"description":"SEC14 like lipid binding 6 [Source:HGNC Symbol;Acc:HGNC:40047]"}, {"versioned_ensembl_gene_id":"ENSG00000216829.6","gene_symbol":"FGF7P4","gene_name":"fibroblast growth factor 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33587]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728195","summary":null,"start":42667506,"end":42668887,"strand":-1,"description":"fibroblast growth factor 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33587]"}, {"versioned_ensembl_gene_id":"ENSG00000181984.11","gene_symbol":"GOLGA8CP","gene_name":"golgin A8 family member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:32375]","synonyms":"GOLGA8C","biotype":"unprocessed_pseudogene","ncbi_id":"729786","summary":null,"start":20562375,"end":20575696,"strand":1,"description":"golgin A8 family member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:32375]"}, {"versioned_ensembl_gene_id":"ENSG00000135447.16","gene_symbol":"PPP1R1A","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 1A [Source:HGNC Symbol;Acc:HGNC:9286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5502","summary":null,"start":54575387,"end":54588659,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 1A [Source:HGNC Symbol;Acc:HGNC:9286]"}, {"versioned_ensembl_gene_id":"ENSG00000248978.2","gene_symbol":"AC009901.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84828573,"end":84829479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235385.1","gene_symbol":"LINC02154","gene_name":"long intergenic non-protein coding RNA 2154 [Source:HGNC Symbol;Acc:HGNC:53015]","synonyms":"GS1-600G8.5","biotype":"lincRNA","ncbi_id":"109729169","summary":null,"start":13266048,"end":13303452,"strand":-1,"description":"long intergenic non-protein coding RNA 2154 [Source:HGNC Symbol;Acc:HGNC:53015]"}, {"versioned_ensembl_gene_id":"ENSG00000254960.2","gene_symbol":"KIRREL3-AS2","gene_name":"KIRREL3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42656]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874251","summary":null,"start":126940746,"end":126945090,"strand":1,"description":"KIRREL3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42656]"}, {"versioned_ensembl_gene_id":"ENSG00000232841.1","gene_symbol":"BRWD1P3","gene_name":"bromodomain and WD repeat domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51530]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480688","summary":null,"start":17033089,"end":17033478,"strand":-1,"description":"bromodomain and WD repeat domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51530]"}, {"versioned_ensembl_gene_id":"ENSG00000270835.2","gene_symbol":"AP001425.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":38204141,"end":38206080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172482.4","gene_symbol":"AGXT","gene_name":"alanine-glyoxylate aminotransferase [Source:HGNC Symbol;Acc:HGNC:341]","synonyms":"SPT,SPAT,PH1,AGXT1,AGT1,AGT","biotype":"protein_coding","ncbi_id":"189","summary":"This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria. [provided by RefSeq, Jul 2008]","start":240868479,"end":240880502,"strand":1,"description":"alanine-glyoxylate aminotransferase [Source:HGNC Symbol;Acc:HGNC:341]"}, {"versioned_ensembl_gene_id":"ENSG00000258550.1","gene_symbol":"OR7E106P","gene_name":"olfactory receptor family 7 subfamily E member 106 pseudogene [Source:HGNC Symbol;Acc:HGNC:15365]","synonyms":"OST215,OR7E40P","biotype":"unprocessed_pseudogene","ncbi_id":"81115","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":51763056,"end":51764076,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 106 pseudogene [Source:HGNC Symbol;Acc:HGNC:15365]"}, {"versioned_ensembl_gene_id":"ENSG00000233420.1","gene_symbol":"AC002127.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88710631,"end":88756725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277445.4","gene_symbol":"CPEB1","gene_name":"cytoplasmic polyadenylation element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21744]","synonyms":"FLJ13203,CPEB","biotype":"protein_coding","ncbi_id":"64506","summary":"This gene encodes a member of the cytoplasmic polyadenylation element binding protein family. This highly conserved protein binds to a specific RNA sequence, called the cytoplasmic polyadenylation element, found in the 3' untranslated region of some mRNAs. The encoded protein functions in both the cytoplasm and the nucleus. It is involved in the regulation of mRNA translation, as well as processing of the 3' untranslated region, and may play a role in cell proliferation and tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":82622289,"end":82720771,"strand":-1,"description":"cytoplasmic polyadenylation element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21744]"}, {"versioned_ensembl_gene_id":"ENSG00000277319.1","gene_symbol":"AL161616.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31483414,"end":31483699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223827.1","gene_symbol":"AL662822.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30506108,"end":30509062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279541.1","gene_symbol":"AC005261.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57293083,"end":57294469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206203.4","gene_symbol":"TSSK2","gene_name":"testis specific serine kinase 2 [Source:HGNC Symbol;Acc:HGNC:11401]","synonyms":"STK22B,SPOGA2,FLJ38613","biotype":"protein_coding","ncbi_id":"23617","summary":"TSSK2 belongs to a family of serine/threonine kinases highly expressed in testis (Hao et al., 2004 [PubMed 15044604]).[supplied by OMIM, Mar 2008]","start":19130808,"end":19132623,"strand":1,"description":"testis specific serine kinase 2 [Source:HGNC Symbol;Acc:HGNC:11401]"}, {"versioned_ensembl_gene_id":"ENSG00000267654.1","gene_symbol":"LINC01882","gene_name":"long intergenic non-protein coding RNA 1882 [Source:HGNC Symbol;Acc:HGNC:52701]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996324","summary":null,"start":12739490,"end":12749421,"strand":-1,"description":"long intergenic non-protein coding RNA 1882 [Source:HGNC Symbol;Acc:HGNC:52701]"}, {"versioned_ensembl_gene_id":"ENSG00000118873.15","gene_symbol":"RAB3GAP2","gene_name":"RAB3 GTPase activating non-catalytic protein subunit 2 [Source:HGNC Symbol;Acc:HGNC:17168]","synonyms":"SPG69,RAB3-GAP150,KIAA0839,DKFZP434D245","biotype":"protein_coding","ncbi_id":"25782","summary":"The protein encoded by this gene belongs to the RAB3 protein family, members of which are involved in regulated exocytosis of neurotransmitters and hormones. This protein forms the Rab3 GTPase-activating complex with RAB3GAP1, where it constitutes the regulatory subunit, whereas the latter functions as the catalytic subunit. This gene has the highest level of expression in the brain, consistent with it having a key role in neurodevelopment. Mutations in this gene are associated with Martsolf syndrome.[provided by RefSeq, Oct 2009]","start":220148293,"end":220272454,"strand":-1,"description":"RAB3 GTPase activating non-catalytic protein subunit 2 [Source:HGNC Symbol;Acc:HGNC:17168]"}, {"versioned_ensembl_gene_id":"ENSG00000213033.4","gene_symbol":"AURKAPS1","gene_name":"aurora kinase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18611]","synonyms":"STK6P,AurAps1","biotype":"transcribed_processed_pseudogene","ncbi_id":"6791","summary":null,"start":220266706,"end":220267917,"strand":-1,"description":"aurora kinase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18611]"}, {"versioned_ensembl_gene_id":"ENSG00000273297.1","gene_symbol":"AC009275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134416290,"end":134432453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162438.11","gene_symbol":"CTRC","gene_name":"chymotrypsin C [Source:HGNC Symbol;Acc:HGNC:2523]","synonyms":"ELA4,CLCR","biotype":"protein_coding","ncbi_id":"11330","summary":"This gene encodes a member of the peptidase S1 family. The encoded protein is a serum calcium-decreasing factor that has chymotrypsin-like protease activity. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":15438439,"end":15449242,"strand":1,"description":"chymotrypsin C [Source:HGNC Symbol;Acc:HGNC:2523]"}, {"versioned_ensembl_gene_id":"ENSG00000225665.4","gene_symbol":"AC073475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120342056,"end":120342647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149269.9","gene_symbol":"PAK1","gene_name":"p21 (RAC1) activated kinase 1 [Source:HGNC Symbol;Acc:HGNC:8590]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5058","summary":"This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Mutations in this gene have been associated with macrocephaly, seizures, and speech delay. Overexpression of this gene is also reported in many cancer types, and particularly in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2020]","start":77321707,"end":77474635,"strand":-1,"description":"p21 (RAC1) activated kinase 1 [Source:HGNC Symbol;Acc:HGNC:8590]"}, {"versioned_ensembl_gene_id":"ENSG00000268635.2","gene_symbol":"AP003680.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77473371,"end":77477030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267097.1","gene_symbol":"SLC14A2-AS1","gene_name":"SLC14A2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927980","summary":null,"start":45423764,"end":45483218,"strand":-1,"description":"SLC14A2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51125]"}, {"versioned_ensembl_gene_id":"ENSG00000047849.21","gene_symbol":"MAP4","gene_name":"microtubule associated protein 4 [Source:HGNC Symbol;Acc:HGNC:6862]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4134","summary":"The protein encoded by this gene is a major non-neuronal microtubule-associated protein. This protein contains a domain similar to the microtubule-binding domains of neuronal microtubule-associated protein (MAP2) and microtubule-associated protein tau (MAPT/TAU). This protein promotes microtubule assembly, and has been shown to counteract destabilization of interphase microtubule catastrophe promotion. Cyclin B was found to interact with this protein, which targets cell division cycle 2 (CDC2) kinase to microtubules. The phosphorylation of this protein affects microtubule properties and cell cycle progression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":47850690,"end":48089272,"strand":-1,"description":"microtubule associated protein 4 [Source:HGNC Symbol;Acc:HGNC:6862]"}, {"versioned_ensembl_gene_id":"ENSG00000150455.13","gene_symbol":"TIRAP","gene_name":"TIR domain containing adaptor protein [Source:HGNC Symbol;Acc:HGNC:17192]","synonyms":"wyatt,Mal","biotype":"protein_coding","ncbi_id":"114609","summary":"The innate immune system recognizes microbial pathogens through Toll-like receptors (TLRs), which identify pathogen-associated molecular patterns. Different TLRs recognize different pathogen-associated molecular patterns and all TLRs have a Toll-interleukin 1 receptor (TIR) domain, which is responsible for signal transduction. The protein encoded by this gene is a TIR adaptor protein involved in the TLR4 signaling pathway of the immune system. It activates NF-kappa-B, MAPK1, MAPK3 and JNK, which then results in cytokine secretion and the inflammatory response. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":126283065,"end":126298845,"strand":1,"description":"TIR domain containing adaptor protein [Source:HGNC Symbol;Acc:HGNC:17192]"}, {"versioned_ensembl_gene_id":"ENSG00000007402.11","gene_symbol":"CACNA2D2","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 2 [Source:HGNC Symbol;Acc:HGNC:1400]","synonyms":"KIAA0558","biotype":"protein_coding","ncbi_id":"9254","summary":"Calcium channels mediate the entry of calcium ions into the cell upon membrane polarization. This gene encodes the alpha-2/delta subunit of the voltage-dependent calcium channel complex. The complex consists of the main channel-forming subunit alpha-1, and auxiliary subunits alpha-2/delta, beta, and gamma. The auxiliary subunits function in the assembly and membrane localization of the complex, and modulate calcium currents and channel activation/inactivation kinetics. The subunit encoded by this gene undergoes post-translational cleavage to yield the extracellular alpha2 peptide and a membrane-anchored delta polypeptide. This subunit is a receptor for the antiepileptic drug, gabapentin. Mutations in this gene are associated with early infantile epileptic encephalopathy. Single nucleotide polymorphisms in this gene are correlated with increased sensitivity to opioid drugs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":50362799,"end":50504244,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit alpha2delta 2 [Source:HGNC Symbol;Acc:HGNC:1400]"}, {"versioned_ensembl_gene_id":"ENSG00000169564.6","gene_symbol":"PCBP1","gene_name":"poly(rC) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8647]","synonyms":"HNRPX,HNRPE1,hnRNP-X,hnRNP-E1","biotype":"protein_coding","ncbi_id":"5093","summary":"This intronless gene is thought to have been generated by retrotransposition of a fully processed PCBP-2 mRNA. This gene and PCBP-2 have paralogues (PCBP3 and PCBP4) which are thought to have arisen as a result of duplication events of entire genes. The protein encoded by this gene appears to be multifunctional. It along with PCBP-2 and hnRNPK corresponds to the major cellular poly(rC)-binding protein. It contains three K-homologous (KH) domains which may be involved in RNA binding. This encoded protein together with PCBP-2 also functions as translational coactivators of poliovirus RNA via a sequence-specific interaction with stem-loop IV of the IRES and promote poliovirus RNA replication by binding to its 5'-terminal cloverleaf structure. It has also been implicated in translational control of the 15-lipoxygenase mRNA, human Papillomavirus type 16 L2 mRNA, and hepatitis A virus RNA. The encoded protein is also suggested to play a part in formation of a sequence-specific alpha-globin mRNP complex which is associated with alpha-globin mRNA stability. [provided by RefSeq, Jul 2008]","start":70087454,"end":70089203,"strand":1,"description":"poly(rC) binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8647]"}, {"versioned_ensembl_gene_id":"ENSG00000204923.3","gene_symbol":"FBXO48","gene_name":"F-box protein 48 [Source:HGNC Symbol;Acc:HGNC:33857]","synonyms":null,"biotype":"protein_coding","ncbi_id":"554251","summary":null,"start":68459419,"end":68467258,"strand":-1,"description":"F-box protein 48 [Source:HGNC Symbol;Acc:HGNC:33857]"}, {"versioned_ensembl_gene_id":"ENSG00000229462.1","gene_symbol":"AC127383.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68445710,"end":68449174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277505.1","gene_symbol":"AC116165.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23140563,"end":23144422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137411.16","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a,VARS2L,DKFZP434L1435,VARS2L","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30908242,"end":30926459,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000123240.16","gene_symbol":"OPTN","gene_name":"optineurin [Source:HGNC Symbol;Acc:HGNC:17142]","synonyms":"GLC1E,FIP2,FIP-2,TFIIIA-INTP,NRP,HYPL,HIP7","biotype":"protein_coding","ncbi_id":"10133","summary":"This gene encodes the coiled-coil containing protein optineurin. Optineurin may play a role in normal-tension glaucoma and adult-onset primary open angle glaucoma. Optineurin interacts with adenovirus E3-14.7K protein and may utilize tumor necrosis factor-alpha or Fas-ligand pathways to mediate apoptosis, inflammation or vasoconstriction. Optineurin may also function in cellular morphogenesis and membrane trafficking, vesicle trafficking, and transcription activation through its interactions with the RAB8, huntingtin, and transcription factor IIIA proteins. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":13099449,"end":13138308,"strand":1,"description":"optineurin [Source:HGNC Symbol;Acc:HGNC:17142]"}, {"versioned_ensembl_gene_id":"ENSG00000151468.10","gene_symbol":"CCDC3","gene_name":"coiled-coil domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23813]","synonyms":"DKFZp761F241","biotype":"protein_coding","ncbi_id":"83643","summary":null,"start":12896625,"end":13099652,"strand":-1,"description":"coiled-coil domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23813]"}, {"versioned_ensembl_gene_id":"ENSG00000132274.15","gene_symbol":"TRIM22","gene_name":"tripartite motif containing 22 [Source:HGNC Symbol;Acc:HGNC:16379]","synonyms":"RNF94,GPSTAF50,STAF50","biotype":"protein_coding","ncbi_id":"10346","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the cytoplasm and its expression is induced by interferon. The protein down-regulates transcription from the HIV-1 LTR promoter region, suggesting that function of this protein may be to mediate interferon's antiviral effects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":5689689,"end":5737089,"strand":1,"description":"tripartite motif containing 22 [Source:HGNC Symbol;Acc:HGNC:16379]"}, {"versioned_ensembl_gene_id":"ENSG00000144231.10","gene_symbol":"POLR2D","gene_name":"RNA polymerase II subunit D [Source:HGNC Symbol;Acc:HGNC:9191]","synonyms":"RBP4","biotype":"protein_coding","ncbi_id":"5433","summary":"This gene encodes the fourth largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. In yeast, this polymerase subunit is associated with the polymerase under suboptimal growth conditions and may have a stress protective role. A sequence for a ribosomal pseudogene is contained within the 3' untranslated region of the transcript from this gene. [provided by RefSeq, Jul 2008]","start":127843551,"end":127858157,"strand":-1,"description":"RNA polymerase II subunit D [Source:HGNC Symbol;Acc:HGNC:9191]"}, {"versioned_ensembl_gene_id":"ENSG00000282765.1","gene_symbol":"LINC01896","gene_name":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645321","summary":null,"start":78976555,"end":78979074,"strand":-1,"description":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]"}, {"versioned_ensembl_gene_id":"ENSG00000224865.7","gene_symbol":"AC009518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131897641,"end":131948953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260802.1","gene_symbol":"LINC00890","gene_name":"long intergenic non-protein coding RNA 890 [Source:HGNC Symbol;Acc:HGNC:48576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401613","summary":null,"start":111511662,"end":111522399,"strand":1,"description":"long intergenic non-protein coding RNA 890 [Source:HGNC Symbol;Acc:HGNC:48576]"}, {"versioned_ensembl_gene_id":"ENSG00000168256.17","gene_symbol":"NKIRAS2","gene_name":"NFKB inhibitor interacting Ras like 2 [Source:HGNC Symbol;Acc:HGNC:17898]","synonyms":"kappaB-Ras2,DKFZP434N1526,KBRAS2","biotype":"protein_coding","ncbi_id":"28511","summary":null,"start":42011382,"end":42025644,"strand":1,"description":"NFKB inhibitor interacting Ras like 2 [Source:HGNC Symbol;Acc:HGNC:17898]"}, {"versioned_ensembl_gene_id":"ENSG00000233563.1","gene_symbol":"OR52E7P","gene_name":"olfactory receptor family 52 subfamily E member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15216]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81264","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5873960,"end":5874892,"strand":1,"description":"olfactory receptor family 52 subfamily E member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15216]"}, {"versioned_ensembl_gene_id":"ENSG00000254069.2","gene_symbol":"AC134698.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43493937,"end":43494762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233813.8","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"PTD017,C6orf14,MRPS18-2,HSPC183","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30607946,"end":30616632,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000120915.13","gene_symbol":"EPHX2","gene_name":"epoxide hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:3402]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2053","summary":"This gene encodes a member of the epoxide hydrolase family. The protein, found in both the cytosol and peroxisomes, binds to specific epoxides and converts them to the corresponding dihydrodiols. Mutations in this gene have been associated with familial hypercholesterolemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]","start":27490779,"end":27545564,"strand":1,"description":"epoxide hydrolase 2 [Source:HGNC Symbol;Acc:HGNC:3402]"}, {"versioned_ensembl_gene_id":"ENSG00000282716.1","gene_symbol":"IGHV1-18","gene_name":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28468","summary":null,"start":106185670,"end":106186165,"strand":-1,"description":"immunoglobulin heavy variable 1-18 [Source:HGNC Symbol;Acc:HGNC:5549]"}, {"versioned_ensembl_gene_id":"ENSG00000168032.8","gene_symbol":"ENTPD3","gene_name":"ectonucleoside triphosphate diphosphohydrolase 3 [Source:HGNC Symbol;Acc:HGNC:3365]","synonyms":"NTPDase-3,HB6,CD39L3","biotype":"protein_coding","ncbi_id":"956","summary":"This gene encodes a plasma membrane-bound divalent cation-dependent E-type nucleotidase. The encoded protein is involved in the regulation of extracellular levels of ATP by hydrolysis of it and other nucleotides. Multiple transcript variants have been described. [provided by RefSeq, May 2014]","start":40387156,"end":40428619,"strand":1,"description":"ectonucleoside triphosphate diphosphohydrolase 3 [Source:HGNC Symbol;Acc:HGNC:3365]"}, {"versioned_ensembl_gene_id":"ENSG00000104081.13","gene_symbol":"BMF","gene_name":"Bcl2 modifying factor [Source:HGNC Symbol;Acc:HGNC:24132]","synonyms":"FLJ00065","biotype":"protein_coding","ncbi_id":"90427","summary":"The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. This protein contains a single BCL2 homology domain 3 (BH3), and has been shown to bind BCL2 proteins and function as an apoptotic activator. This protein is found to be sequestered to myosin V motors by its association with dynein light chain 2, which may be important for sensing intracellular damage and triggering apoptosis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":40087890,"end":40108892,"strand":-1,"description":"Bcl2 modifying factor [Source:HGNC Symbol;Acc:HGNC:24132]"}, {"versioned_ensembl_gene_id":"ENSG00000267336.1","gene_symbol":"EIF4A2P1","gene_name":"eukaryotic translation initiation factor 4A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646171","summary":null,"start":12912844,"end":12913906,"strand":1,"description":"eukaryotic translation initiation factor 4A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37929]"}, {"versioned_ensembl_gene_id":"ENSG00000156687.10","gene_symbol":"UNC5D","gene_name":"unc-5 netrin receptor D [Source:HGNC Symbol;Acc:HGNC:18634]","synonyms":"Unc5h4,KIAA1777","biotype":"protein_coding","ncbi_id":"137970","summary":null,"start":35235457,"end":35796550,"strand":1,"description":"unc-5 netrin receptor D [Source:HGNC Symbol;Acc:HGNC:18634]"}, {"versioned_ensembl_gene_id":"ENSG00000223421.1","gene_symbol":"AL354854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31165618,"end":31166980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142303.13","gene_symbol":"ADAMTS10","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 10 [Source:HGNC Symbol;Acc:HGNC:13201]","synonyms":"ADAM-TS10","biotype":"protein_coding","ncbi_id":"81794","summary":"This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq, Jul 2008]","start":8580242,"end":8610735,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 10 [Source:HGNC Symbol;Acc:HGNC:13201]"}, {"versioned_ensembl_gene_id":"ENSG00000171056.7","gene_symbol":"SOX7","gene_name":"SRY-box 7 [Source:HGNC Symbol;Acc:HGNC:18196]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83595","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The protein may play a role in tumorigenesis. A similar protein in mice is involved in the regulation of the wingless-type MMTV integration site family (Wnt) pathway. [provided by RefSeq, Jul 2008]","start":10723768,"end":10730512,"strand":-1,"description":"SRY-box 7 [Source:HGNC Symbol;Acc:HGNC:18196]"}, {"versioned_ensembl_gene_id":"ENSG00000186480.12","gene_symbol":"INSIG1","gene_name":"insulin induced gene 1 [Source:HGNC Symbol;Acc:HGNC:6083]","synonyms":"MGC1405,CL-6","biotype":"protein_coding","ncbi_id":"3638","summary":"This gene encodes an endoplasmic reticulum membrane protein that regulates cholesterol metabolism, lipogenesis, and glucose homeostasis. The encoded protein has six transmembrane helices which contain an effector protein binding site. It binds the sterol-sensing domains of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP) and 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), and is essential for the sterol-mediated trafficking of these two proteins. It promotes the endoplasmic reticulum retention of SCAP and the ubiquitin-mediated degradation of HMG-CoA reductase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":155297776,"end":155310235,"strand":1,"description":"insulin induced gene 1 [Source:HGNC Symbol;Acc:HGNC:6083]"}, {"versioned_ensembl_gene_id":"ENSG00000279442.1","gene_symbol":"AP000542.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15298378,"end":15304556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253263.1","gene_symbol":"AP003354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102891876,"end":102893608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266527.1","gene_symbol":"AC005697.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27874645,"end":27881237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280828.1","gene_symbol":"AC090114.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128533652,"end":128615970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277646.1","gene_symbol":"AL353684.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29317833,"end":29318952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104365.13","gene_symbol":"IKBKB","gene_name":"inhibitor of nuclear factor kappa B kinase subunit beta [Source:HGNC Symbol;Acc:HGNC:5960]","synonyms":"NFKBIKB,IKKB,IKK2,IKK-beta","biotype":"protein_coding","ncbi_id":"3551","summary":"The protein encoded by this gene phosphorylates the inhibitor in the inhibitor/NF-kappa-B complex, causing dissociation of the inhibitor and activation of NF-kappa-B. The encoded protein itself is found in a complex of proteins. Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Sep 2011]","start":42271302,"end":42332653,"strand":1,"description":"inhibitor of nuclear factor kappa B kinase subunit beta [Source:HGNC Symbol;Acc:HGNC:5960]"}, {"versioned_ensembl_gene_id":"ENSG00000178726.6","gene_symbol":"THBD","gene_name":"thrombomodulin [Source:HGNC Symbol;Acc:HGNC:11784]","synonyms":"CD141","biotype":"protein_coding","ncbi_id":"7056","summary":"The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia. [provided by RefSeq, Jul 2008]","start":23045633,"end":23049741,"strand":-1,"description":"thrombomodulin [Source:HGNC Symbol;Acc:HGNC:11784]"}, {"versioned_ensembl_gene_id":"ENSG00000283427.1","gene_symbol":"AC006453.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89533185,"end":89547106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174482.10","gene_symbol":"LINGO2","gene_name":"leucine rich repeat and Ig domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21207]","synonyms":"LRRN6C,LERN3","biotype":"protein_coding","ncbi_id":"158038","summary":null,"start":27948078,"end":28670286,"strand":-1,"description":"leucine rich repeat and Ig domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21207]"}, {"versioned_ensembl_gene_id":"ENSG00000236907.1","gene_symbol":"AC023141.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57817601,"end":57818012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206493.7","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30478970,"end":30483708,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000145390.11","gene_symbol":"USP53","gene_name":"ubiquitin specific peptidase 53 [Source:HGNC Symbol;Acc:HGNC:29255]","synonyms":"KIAA1350","biotype":"protein_coding","ncbi_id":"54532","summary":null,"start":119212587,"end":119295517,"strand":1,"description":"ubiquitin specific peptidase 53 [Source:HGNC Symbol;Acc:HGNC:29255]"}, {"versioned_ensembl_gene_id":"ENSG00000229760.1","gene_symbol":"MTCO1P52","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:52117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075227","summary":null,"start":55178207,"end":55178737,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:52117]"}, {"versioned_ensembl_gene_id":"ENSG00000260390.1","gene_symbol":"AL360014.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27829276,"end":27844481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276333.2","gene_symbol":"HS3ST6","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:14178]","synonyms":"HS3ST5","biotype":"protein_coding","ncbi_id":"64711","summary":null,"start":1913487,"end":1920464,"strand":-1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:14178]"}, {"versioned_ensembl_gene_id":"ENSG00000271546.1","gene_symbol":"AC245389.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148795797,"end":148796325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113597.17","gene_symbol":"TRAPPC13","gene_name":"trafficking protein particle complex 13 [Source:HGNC Symbol;Acc:HGNC:25828]","synonyms":"C5orf44,MGC48585,FLJ26957,FLJ13611","biotype":"protein_coding","ncbi_id":"80006","summary":null,"start":65624716,"end":65666233,"strand":1,"description":"trafficking protein particle complex 13 [Source:HGNC Symbol;Acc:HGNC:25828]"}, {"versioned_ensembl_gene_id":"ENSG00000180592.16","gene_symbol":"SKIDA1","gene_name":"SKI/DACH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32697]","synonyms":"FLJ45187,C10orf140","biotype":"protein_coding","ncbi_id":"387640","summary":null,"start":21513478,"end":21526368,"strand":-1,"description":"SKI/DACH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:32697]"}, {"versioned_ensembl_gene_id":"ENSG00000163428.3","gene_symbol":"LRRC58","gene_name":"leucine rich repeat containing 58 [Source:HGNC Symbol;Acc:HGNC:26968]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116064","summary":null,"start":120324509,"end":120349339,"strand":-1,"description":"leucine rich repeat containing 58 [Source:HGNC Symbol;Acc:HGNC:26968]"}, {"versioned_ensembl_gene_id":"ENSG00000253487.1","gene_symbol":"IGKV2-36","gene_name":"immunoglobulin kappa variable 2-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5786]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28918","summary":null,"start":89295233,"end":89295455,"strand":-1,"description":"immunoglobulin kappa variable 2-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5786]"}, {"versioned_ensembl_gene_id":"ENSG00000226824.6","gene_symbol":"AC006001.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":66654538,"end":66669855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187325.4","gene_symbol":"TAF9B","gene_name":"TATA-box binding protein associated factor 9b [Source:HGNC Symbol;Acc:HGNC:17306]","synonyms":"DN7,DN-7,TFIID-31,TAFII31L,TAF9L","biotype":"protein_coding","ncbi_id":"51616","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes a protein that is similar to one of the small subunits of TFIID, TBP-associated factor 9, and is also a subunit of TFIID. TAF9 and TAF9b share some functions but also have distinct roles in the transcriptional regulatory process. [provided by RefSeq, Jul 2008]","start":78129748,"end":78139706,"strand":-1,"description":"TATA-box binding protein associated factor 9b [Source:HGNC Symbol;Acc:HGNC:17306]"}, {"versioned_ensembl_gene_id":"ENSG00000231028.8","gene_symbol":"LINC00271","gene_name":"long intergenic non-protein coding RNA 271 [Source:HGNC Symbol;Acc:HGNC:32526]","synonyms":"NCRNA00271,C6orf217","biotype":"lincRNA","ncbi_id":"100131814","summary":null,"start":135497801,"end":135716055,"strand":1,"description":"long intergenic non-protein coding RNA 271 [Source:HGNC Symbol;Acc:HGNC:32526]"}, {"versioned_ensembl_gene_id":"ENSG00000282469.1","gene_symbol":"LINC00254","gene_name":"long intergenic non-protein coding RNA 254 [Source:NCBI gene;Acc:64735]","synonyms":"NCRNA00254,C16orf32","biotype":"lincRNA","ncbi_id":"64735","summary":null,"start":1880310,"end":1886269,"strand":-1,"description":"long intergenic non-protein coding RNA 254 [Source:NCBI gene;Acc:64735]"}, {"versioned_ensembl_gene_id":"ENSG00000226540.2","gene_symbol":"GAPDHP73","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:22956]","synonyms":"GAPDL19,GAPDHL19","biotype":"processed_pseudogene","ncbi_id":"442262","summary":null,"start":135619165,"end":135620171,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:22956]"}, {"versioned_ensembl_gene_id":"ENSG00000117569.18","gene_symbol":"PTBP2","gene_name":"polypyrimidine tract binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17662]","synonyms":"PTBLP,PTB,nPTB,brPTB","biotype":"protein_coding","ncbi_id":"58155","summary":"The protein encoded by this gene binds to intronic polypyrimidine clusters in pre-mRNA molecules and is implicated in controlling the assembly of other splicing-regulatory proteins. This protein is very similar to the polypyrimidine tract binding protein (PTB) but most of its isoforms are expressed primarily in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":96721665,"end":96823738,"strand":1,"description":"polypyrimidine tract binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17662]"}, {"versioned_ensembl_gene_id":"ENSG00000243067.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"beta1i,PSMB6i,LMP2,RING12","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32766454,"end":32801905,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000263604.1","gene_symbol":"AC015688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27683946,"end":27684144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239218.2","gene_symbol":"RPS20P22","gene_name":"ribosomal protein S20 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36379]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271087","summary":null,"start":38434347,"end":38435664,"strand":-1,"description":"ribosomal protein S20 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36379]"}, {"versioned_ensembl_gene_id":"ENSG00000264240.1","gene_symbol":"CPDP1","gene_name":"carboxypeptidase D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:53102]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729163","summary":null,"start":27677805,"end":27678087,"strand":-1,"description":"carboxypeptidase D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:53102]"}, {"versioned_ensembl_gene_id":"ENSG00000255201.1","gene_symbol":"AC087623.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38421889,"end":38426096,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230260.1","gene_symbol":"AL136322.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197437976,"end":197447469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271699.5","gene_symbol":"SNX29P2","gene_name":"sorting nexin 29 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31914]","synonyms":"RUNDC2C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440352","summary":null,"start":29350746,"end":29370272,"strand":1,"description":"sorting nexin 29 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31914]"}, {"versioned_ensembl_gene_id":"ENSG00000284685.1","gene_symbol":"AC009093.10","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29139379,"end":29331304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237335.8","gene_symbol":"PFDN6","gene_name":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]","synonyms":"HKE2,H2-KE2,PFD6,KE-2","biotype":"protein_coding","ncbi_id":"10471","summary":"PFDN6 is a subunit of the heteromeric prefoldin complex that chaperones nascent actin (see MIM 102560) and alpha- and beta-tubulin (see MIM 602529 and MIM 191130, respectively) chains pending their transfer to the cytosolic chaperonin containing TCP1 (MIM 186980) (CCT) complex (Hansen et al., 1999 [PubMed 10209023]).[supplied by OMIM, Jul 2010]","start":33210906,"end":33220005,"strand":1,"description":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]"}, {"versioned_ensembl_gene_id":"ENSG00000250673.2","gene_symbol":"AC097372.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":146214515,"end":146230878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242715.7","gene_symbol":"CCDC169","gene_name":"coiled-coil domain containing 169 [Source:HGNC Symbol;Acc:HGNC:34361]","synonyms":"RP11-251J8.1,LOC728591,C13orf38","biotype":"protein_coding","ncbi_id":"728591","summary":null,"start":36222008,"end":36297840,"strand":-1,"description":"coiled-coil domain containing 169 [Source:HGNC Symbol;Acc:HGNC:34361]"}, {"versioned_ensembl_gene_id":"ENSG00000160208.12","gene_symbol":"RRP1B","gene_name":"ribosomal RNA processing 1B [Source:HGNC Symbol;Acc:HGNC:23818]","synonyms":"RRP1,PPP1R136,Nnp1,KIAA0179","biotype":"protein_coding","ncbi_id":"23076","summary":null,"start":43659548,"end":43696079,"strand":1,"description":"ribosomal RNA processing 1B [Source:HGNC Symbol;Acc:HGNC:23818]"}, {"versioned_ensembl_gene_id":"ENSG00000136536.14","gene_symbol":"MARCH7","gene_name":"membrane associated ring-CH-type finger 7 [Source:HGNC Symbol;Acc:HGNC:17393]","synonyms":"MARCH-VII,AXOT,RNF177","biotype":"protein_coding","ncbi_id":"64844","summary":"MARCH7 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Mar 2010]","start":159712457,"end":159771027,"strand":1,"description":"membrane associated ring-CH-type finger 7 [Source:HGNC Symbol;Acc:HGNC:17393]"}, {"versioned_ensembl_gene_id":"ENSG00000248508.6","gene_symbol":"SRP14-AS1","gene_name":"SRP14 antisense RNA1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48619]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100131089","summary":null,"start":40039311,"end":40067290,"strand":1,"description":"SRP14 antisense RNA1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48619]"}, {"versioned_ensembl_gene_id":"ENSG00000229978.1","gene_symbol":"PRAMEF36P","gene_name":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645354","summary":null,"start":13128818,"end":13131615,"strand":1,"description":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]"}, {"versioned_ensembl_gene_id":"ENSG00000134376.15","gene_symbol":"CRB1","gene_name":"crumbs 1, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:2343]","synonyms":"LCA8,RP12","biotype":"protein_coding","ncbi_id":"23418","summary":"This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternate splicing results in multiple transcript variants, some protein coding and some non-protein coding.[provided by RefSeq, Apr 2012]","start":197268204,"end":197478455,"strand":1,"description":"crumbs 1, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:2343]"}, {"versioned_ensembl_gene_id":"ENSG00000250709.1","gene_symbol":"CCDC169-SOHLH2","gene_name":"CCDC169-SOHLH2 readthrough [Source:HGNC Symbol;Acc:HGNC:38866]","synonyms":"C13orf38-SOHLH2","biotype":"protein_coding","ncbi_id":"100526761","summary":"This locus represents naturally occurring read-through transcription between the neighboring C13orf38 (chromosome 13 open reading frame 38) and SOHLH2 (spermatogenesis and oogenesis specific basic helix-loop-helix 2) genes. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]","start":36168794,"end":36297842,"strand":-1,"description":"CCDC169-SOHLH2 readthrough [Source:HGNC Symbol;Acc:HGNC:38866]"}, {"versioned_ensembl_gene_id":"ENSG00000271500.1","gene_symbol":"AC005183.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1695830,"end":1698044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281693.1","gene_symbol":"AC217775.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46854433,"end":46858400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137161.16","gene_symbol":"CNPY3","gene_name":"canopy FGF signaling regulator 3 [Source:HGNC Symbol;Acc:HGNC:11968]","synonyms":"TNRC5,CAG4A","biotype":"protein_coding","ncbi_id":"10695","summary":"This gene encodes a protein that binds members of the toll-like receptor protein family and functions as a chaperone to aid in folding and export of these proteins. Alternative splicing results in multiple transcript variants. Naturally occuring readthrough transcription occurs between this locus and the downstream GNMT (glycine N-methyltransferase) gene and is represented with GeneID:107080644. [provided by RefSeq, Jan 2016]","start":42929192,"end":42939287,"strand":1,"description":"canopy FGF signaling regulator 3 [Source:HGNC Symbol;Acc:HGNC:11968]"}, {"versioned_ensembl_gene_id":"ENSG00000203867.7","gene_symbol":"RBM20","gene_name":"RNA binding motif protein 20 [Source:HGNC Symbol;Acc:HGNC:27424]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282996","summary":"This gene encodes a protein that binds RNA and regulates splicing. Mutations in this gene have been associated with familial dilated cardiomyopathy. [provided by RefSeq, Apr 2014]","start":110644397,"end":110839469,"strand":1,"description":"RNA binding motif protein 20 [Source:HGNC Symbol;Acc:HGNC:27424]"}, {"versioned_ensembl_gene_id":"ENSG00000267257.1","gene_symbol":"AC105105.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58535415,"end":58538552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278960.1","gene_symbol":"AL022329.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25756318,"end":25756669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133454.15","gene_symbol":"MYO18B","gene_name":"myosin XVIIIB [Source:HGNC Symbol;Acc:HGNC:18150]","synonyms":"BK125H2.1","biotype":"protein_coding","ncbi_id":"84700","summary":"The protein encoded by this gene may regulate muscle-specific genes when in the nucleus and may influence intracellular trafficking when in the cytoplasm. The encoded protein functions as a homodimer and may interact with F actin. Mutations in this gene are associated with lung cancer. [provided by RefSeq, Jul 2008]","start":25742144,"end":26031041,"strand":1,"description":"myosin XVIIIB [Source:HGNC Symbol;Acc:HGNC:18150]"}, {"versioned_ensembl_gene_id":"ENSG00000232464.1","gene_symbol":"Z98949.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25959074,"end":25983526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280960.1","gene_symbol":"OR7E157P","gene_name":"olfactory receptor family 7 subfamily E member 157 pseudogene [Source:HGNC Symbol;Acc:HGNC:31231]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403219","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7583982,"end":7584892,"strand":1,"description":"olfactory receptor family 7 subfamily E member 157 pseudogene [Source:HGNC Symbol;Acc:HGNC:31231]"}, {"versioned_ensembl_gene_id":"ENSG00000282368.1","gene_symbol":"AC243913.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28596172,"end":28599296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240438.2","gene_symbol":"OFD1P5Y","gene_name":"OFD1 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:23877]","synonyms":"OFDYP5,OFD1PY5,OFD1P5","biotype":"unprocessed_pseudogene","ncbi_id":"386689","summary":null,"start":18582063,"end":18629077,"strand":-1,"description":"OFD1 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:23877]"}, {"versioned_ensembl_gene_id":"ENSG00000281283.1","gene_symbol":"MAPK8IP1P1","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]","synonyms":"MAPK8IPP,PRKM8IPP","biotype":"processed_pseudogene","ncbi_id":"644253","summary":null,"start":46495985,"end":46497453,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]"}, {"versioned_ensembl_gene_id":"ENSG00000121022.13","gene_symbol":"COPS5","gene_name":"COP9 signalosome subunit 5 [Source:HGNC Symbol;Acc:HGNC:2240]","synonyms":"MOV-34,JAB1,CSN5,SGN5","biotype":"protein_coding","ncbi_id":"10987","summary":"The protein encoded by this gene is one of the eight subunits of COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. This protein is reported to be involved in the degradation of cyclin-dependent kinase inhibitor CDKN1B/p27Kip1. It is also known to be an coactivator that increases the specificity of JUN/AP1 transcription factors. [provided by RefSeq, Jul 2008]","start":67043079,"end":67083783,"strand":-1,"description":"COP9 signalosome subunit 5 [Source:HGNC Symbol;Acc:HGNC:2240]"}, {"versioned_ensembl_gene_id":"ENSG00000237768.2","gene_symbol":"AL731563.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73071295,"end":73074008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224467.1","gene_symbol":"AC009313.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161096231,"end":161160224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147606.8","gene_symbol":"SLC26A7","gene_name":"solute carrier family 26 member 7 [Source:HGNC Symbol;Acc:HGNC:14467]","synonyms":"SUT2","biotype":"protein_coding","ncbi_id":"115111","summary":"This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Aug 2013]","start":91209494,"end":91398152,"strand":1,"description":"solute carrier family 26 member 7 [Source:HGNC Symbol;Acc:HGNC:14467]"}, {"versioned_ensembl_gene_id":"ENSG00000066777.8","gene_symbol":"ARFGEF1","gene_name":"ADP ribosylation factor guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:15772]","synonyms":"BIG1,ARFGEP1,p200,DKFZP434L057","biotype":"protein_coding","ncbi_id":"10565","summary":"ADP-ribosylation factors (ARFs) play an important role in intracellular vesicular trafficking. The protein encoded by this gene is involved in the activation of ARFs by accelerating replacement of bound GDP with GTP. It contains a Sec7 domain, which may be responsible for guanine-nucleotide exchange activity and also brefeldin A inhibition. [provided by RefSeq, Aug 2011]","start":67173511,"end":67343677,"strand":-1,"description":"ADP ribosylation factor guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:15772]"}, {"versioned_ensembl_gene_id":"ENSG00000111046.3","gene_symbol":"MYF6","gene_name":"myogenic factor 6 [Source:HGNC Symbol;Acc:HGNC:7566]","synonyms":"MRF4,bHLHc4","biotype":"protein_coding","ncbi_id":"4618","summary":"The protein encoded by this gene is a probable basic helix-loop-helix (bHLH) DNA binding protein involved in muscle differentiation. The encoded protein likely acts as a heterodimer with another bHLH protein. Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM). [provided by RefSeq, May 2010]","start":80707498,"end":80709474,"strand":1,"description":"myogenic factor 6 [Source:HGNC Symbol;Acc:HGNC:7566]"}, {"versioned_ensembl_gene_id":"ENSG00000159921.14","gene_symbol":"GNE","gene_name":"glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase [Source:HGNC Symbol;Acc:HGNC:23657]","synonyms":"Uae1,IBM2","biotype":"protein_coding","ncbi_id":"10020","summary":"The protein encoded by this gene is a bifunctional enzyme that initiates and regulates the biosynthesis of N-acetylneuraminic acid (NeuAc), a precursor of sialic acids. It is a rate-limiting enzyme in the sialic acid biosynthetic pathway. Sialic acid modification of cell surface molecules is crucial for their function in many biologic processes, including cell adhesion and signal transduction. Differential sialylation of cell surface molecules is also implicated in the tumorigenicity and metastatic behavior of malignant cells. Mutations in this gene are associated with sialuria, autosomal recessive inclusion body myopathy, and Nonaka myopathy. Alternative splicing of this gene results in transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":36214441,"end":36277056,"strand":-1,"description":"glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase [Source:HGNC Symbol;Acc:HGNC:23657]"}, {"versioned_ensembl_gene_id":"ENSG00000215283.3","gene_symbol":"HMGB3P24","gene_name":"high mobility group box 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39316]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646993","summary":null,"start":36303499,"end":36304924,"strand":-1,"description":"high mobility group box 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39316]"}, {"versioned_ensembl_gene_id":"ENSG00000136682.14","gene_symbol":"CBWD2","gene_name":"COBW domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17907]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150472","summary":null,"start":113437691,"end":113496189,"strand":1,"description":"COBW domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17907]"}, {"versioned_ensembl_gene_id":"ENSG00000157259.6","gene_symbol":"GATAD1","gene_name":"GATA zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29941]","synonyms":"ODAG,FLJ22489,RG083M05.2","biotype":"protein_coding","ncbi_id":"57798","summary":"The protein encoded by this gene contains a zinc finger at the N-terminus, and is thought to bind to a histone modification site that regulates gene expression. Mutations in this gene have been associated with autosomal recessive dilated cardiomyopathy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]","start":92447453,"end":92458836,"strand":1,"description":"GATA zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29941]"}, {"versioned_ensembl_gene_id":"ENSG00000136044.11","gene_symbol":"APPL2","gene_name":"adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2 [Source:HGNC Symbol;Acc:HGNC:18242]","synonyms":"FLJ10659,DIP13B","biotype":"protein_coding","ncbi_id":"55198","summary":"The protein encoded by this gene is one of two effectors of the small GTPase RAB5A/Rab5, which are involved in a signal transduction pathway. Both effectors contain an N-terminal Bin/Amphiphysin/Rvs (BAR) domain, a central pleckstrin homology (PH) domain, and a C-terminal phosphotyrosine binding (PTB) domain, and they bind the Rab5 through the BAR domain. They are associated with endosomal membranes and can be translocated to the nucleus in response to the EGF stimulus. They interact with the NuRD/MeCP1 complex (nucleosome remodeling and deacetylase /methyl-CpG-binding protein 1 complex) and are required for efficient cell proliferation. A chromosomal aberration t(12;22)(q24.1;q13.3) involving this gene and the PSAP2 gene results in 22q13.3 deletion syndrome, also known as Phelan-McDermid syndrome. [provided by RefSeq, Oct 2011]","start":105173296,"end":105236238,"strand":-1,"description":"adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2 [Source:HGNC Symbol;Acc:HGNC:18242]"}, {"versioned_ensembl_gene_id":"ENSG00000261764.1","gene_symbol":"KRT18P18","gene_name":"keratin 18 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:33386]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"342374","summary":null,"start":72728616,"end":72729894,"strand":1,"description":"keratin 18 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:33386]"}, {"versioned_ensembl_gene_id":"ENSG00000279206.1","gene_symbol":"AC004943.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72772673,"end":72773272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284675.1","gene_symbol":"AC116667.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73123296,"end":73137580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277709.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54883911,"end":54885779,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000181215.14","gene_symbol":"C4orf50","gene_name":"chromosome 4 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:33766]","synonyms":"FLJ46481","biotype":"protein_coding","ncbi_id":"389197","summary":null,"start":5897373,"end":6018507,"strand":-1,"description":"chromosome 4 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:33766]"}, {"versioned_ensembl_gene_id":"ENSG00000178055.11","gene_symbol":"PRSS42","gene_name":"protease, serine 42 [Source:HGNC Symbol;Acc:HGNC:30716]","synonyms":"TESSP2","biotype":"protein_coding","ncbi_id":"339906","summary":"This gene encodes a member of a cluster of testis-specific serine proteases. The orthologous mouse gene is expressed during meiosis in pachytene spermatocytes and is required for germ cell survival. This human locus is represented as a pseudogene because it contains an early stop codon that disrupts the trypsin domain, compared to the mouse ortholog. [provided by RefSeq, Jan 2019]","start":46829542,"end":46834095,"strand":-1,"description":"protease, serine 42 [Source:HGNC Symbol;Acc:HGNC:30716]"}, {"versioned_ensembl_gene_id":"ENSG00000139514.12","gene_symbol":"SLC7A1","gene_name":"solute carrier family 7 member 1 [Source:HGNC Symbol;Acc:HGNC:11057]","synonyms":"HCAT1,ERR,CAT-1,ATRC1,REC1L","biotype":"protein_coding","ncbi_id":"6541","summary":null,"start":29509410,"end":29595688,"strand":-1,"description":"solute carrier family 7 member 1 [Source:HGNC Symbol;Acc:HGNC:11057]"}, {"versioned_ensembl_gene_id":"ENSG00000260725.1","gene_symbol":"AC005307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28418483,"end":28429490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271122.1","gene_symbol":"AC018647.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35695214,"end":35699413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116701.14","gene_symbol":"NCF2","gene_name":"neutrophil cytosolic factor 2 [Source:HGNC Symbol;Acc:HGNC:7661]","synonyms":"p67phox,NOXA2","biotype":"protein_coding","ncbi_id":"4688","summary":"This gene encodes neutrophil cytosolic factor 2, the 67-kilodalton cytosolic subunit of the multi-protein NADPH oxidase complex found in neutrophils. This oxidase produces a burst of superoxide which is delivered to the lumen of the neutrophil phagosome. Mutations in this gene, as well as in other NADPH oxidase subunits, can result in chronic granulomatous disease, a disease that causes recurrent infections by catalase-positive organisms. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2010]","start":183555563,"end":183590876,"strand":-1,"description":"neutrophil cytosolic factor 2 [Source:HGNC Symbol;Acc:HGNC:7661]"}, {"versioned_ensembl_gene_id":"ENSG00000109736.14","gene_symbol":"MFSD10","gene_name":"major facilitator superfamily domain containing 10 [Source:HGNC Symbol;Acc:HGNC:16894]","synonyms":"TETRAN,IT10C3","biotype":"protein_coding","ncbi_id":"10227","summary":"This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein likely functions in efflux of organic anions, including the non-steroidal anti-inflammatory drugs indomethacin and diclofenac. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":2930561,"end":2934859,"strand":-1,"description":"major facilitator superfamily domain containing 10 [Source:HGNC Symbol;Acc:HGNC:16894]"}, {"versioned_ensembl_gene_id":"ENSG00000278080.1","gene_symbol":"SPDYE15P","gene_name":"speedy/RINGO cell cycle regulator family member E15, pseudogene [Source:HGNC Symbol;Acc:HGNC:51511]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105180391","summary":null,"start":75337162,"end":75343013,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E15, pseudogene [Source:HGNC Symbol;Acc:HGNC:51511]"}, {"versioned_ensembl_gene_id":"ENSG00000047230.14","gene_symbol":"CTPS2","gene_name":"CTP synthase 2 [Source:HGNC Symbol;Acc:HGNC:2520]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56474","summary":"The protein encoded by this gene catalyzes the formation of CTP from UTP with the concomitant deamination of glutamine to glutamate. This protein is the rate-limiting enzyme in the synthesis of cytosine nucleotides, which play an important role in various metabolic processes and provide the precursors necessary for the synthesis of RNA and DNA. Cancer cells that exhibit increased cell proliferation also exhibit an increased activity of this encoded protein. Thus, this protein is an attractive target for selective chemotherapy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":16588003,"end":16712936,"strand":-1,"description":"CTP synthase 2 [Source:HGNC Symbol;Acc:HGNC:2520]"}, {"versioned_ensembl_gene_id":"ENSG00000278807.1","gene_symbol":"SPDYE14P","gene_name":"speedy/RINGO cell cycle regulator family member E14, pseudogene [Source:HGNC Symbol;Acc:HGNC:51510]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"641776","summary":null,"start":75309144,"end":75315046,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E14, pseudogene [Source:HGNC Symbol;Acc:HGNC:51510]"}, {"versioned_ensembl_gene_id":"ENSG00000114646.9","gene_symbol":"CSPG5","gene_name":"chondroitin sulfate proteoglycan 5 [Source:HGNC Symbol;Acc:HGNC:2467]","synonyms":"NGC","biotype":"protein_coding","ncbi_id":"10675","summary":"The protein encoded by this gene is a proteoglycan that may function as a neural growth and differentiation factor. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":47562239,"end":47580792,"strand":-1,"description":"chondroitin sulfate proteoglycan 5 [Source:HGNC Symbol;Acc:HGNC:2467]"}, {"versioned_ensembl_gene_id":"ENSG00000278183.4","gene_symbol":"ABCC1","gene_name":"ATP binding cassette subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:51]","synonyms":"MRP1,MRP,GS-X","biotype":"protein_coding","ncbi_id":"4363","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra-and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This full transporter is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a multispecific organic anion transporter, with oxidized glutatione, cysteinyl leukotrienes, and activated aflatoxin B1 as substrates. This protein also transports glucuronides and sulfate conjugates of steroid hormones and bile salts. Alternatively spliced variants of this gene have been described but their full-length nature is unknown. [provided by RefSeq, Apr 2012]","start":16034690,"end":16228109,"strand":1,"description":"ATP binding cassette subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:51]"}, {"versioned_ensembl_gene_id":"ENSG00000232912.5","gene_symbol":"AL096855.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8424645,"end":8434838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263429.3","gene_symbol":"LINC00675","gene_name":"long intergenic non-protein coding RNA 675 [Source:HGNC Symbol;Acc:HGNC:44356]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100289255","summary":null,"start":10794913,"end":10804099,"strand":-1,"description":"long intergenic non-protein coding RNA 675 [Source:HGNC Symbol;Acc:HGNC:44356]"}, {"versioned_ensembl_gene_id":"ENSG00000183117.18","gene_symbol":"CSMD1","gene_name":"CUB and Sushi multiple domains 1 [Source:HGNC Symbol;Acc:HGNC:14026]","synonyms":"PPP1R24,KIAA1890","biotype":"protein_coding","ncbi_id":"64478","summary":null,"start":2935353,"end":4994972,"strand":-1,"description":"CUB and Sushi multiple domains 1 [Source:HGNC Symbol;Acc:HGNC:14026]"}, {"versioned_ensembl_gene_id":"ENSG00000204683.10","gene_symbol":"C10orf113","gene_name":"chromosome 10 open reading frame 113 [Source:HGNC Symbol;Acc:HGNC:31447]","synonyms":"bA165O3.1","biotype":"protein_coding","ncbi_id":"387638","summary":null,"start":21125763,"end":21146559,"strand":-1,"description":"chromosome 10 open reading frame 113 [Source:HGNC Symbol;Acc:HGNC:31447]"}, {"versioned_ensembl_gene_id":"ENSG00000235940.1","gene_symbol":"MTND1P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873340","summary":null,"start":20804293,"end":20804577,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42070]"}, {"versioned_ensembl_gene_id":"ENSG00000278475.1","gene_symbol":"AC009464.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45789189,"end":45789657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270429.1","gene_symbol":"KNOP1P2","gene_name":"lysine rich nucleolar protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420898","summary":null,"start":45880950,"end":45882266,"strand":-1,"description":"lysine rich nucleolar protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48920]"}, {"versioned_ensembl_gene_id":"ENSG00000142599.17","gene_symbol":"RERE","gene_name":"arginine-glutamic acid dipeptide repeats [Source:HGNC Symbol;Acc:HGNC:9965]","synonyms":"ARP,ARG,KIAA0458,DNB1,ATN1L","biotype":"protein_coding","ncbi_id":"473","summary":"This gene encodes a member of the atrophin family of arginine-glutamic acid (RE) dipeptide repeat-containing proteins. The encoded protein co-localizes with a transcription factor in the nucleus, and its overexpression triggers apoptosis. A similar protein in mouse associates with histone deacetylase and is thought to function as a transcriptional co-repressor during embryonic development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":8352397,"end":8817643,"strand":-1,"description":"arginine-glutamic acid dipeptide repeats [Source:HGNC Symbol;Acc:HGNC:9965]"}, {"versioned_ensembl_gene_id":"ENSG00000228502.1","gene_symbol":"EEF1A1P11","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:3206]","synonyms":"EEF1AL9","biotype":"processed_pseudogene","ncbi_id":"440595","summary":null,"start":96446930,"end":96448318,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:3206]"}, {"versioned_ensembl_gene_id":"ENSG00000231292.6","gene_symbol":"IGKV1OR2-108","gene_name":"immunoglobulin kappa variable 1/OR2-108 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5767]","synonyms":"IGO1,IGKV1OR2108,IGKV1/OR2-108","biotype":"IG_V_gene","ncbi_id":"28862","summary":null,"start":113406396,"end":113406872,"strand":1,"description":"immunoglobulin kappa variable 1/OR2-108 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5767]"}, {"versioned_ensembl_gene_id":"ENSG00000231624.2","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31156133,"end":31157469,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000227210.1","gene_symbol":"AC079145.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19990217,"end":20004210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218175.2","gene_symbol":"AC016739.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176200908,"end":176201252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233121.1","gene_symbol":"VN1R20P","gene_name":"vomeronasal 1 receptor 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:37335]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100312775","summary":null,"start":13926813,"end":13927778,"strand":1,"description":"vomeronasal 1 receptor 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:37335]"}, {"versioned_ensembl_gene_id":"ENSG00000177030.16","gene_symbol":"DEAF1","gene_name":"DEAF1, transcription factor [Source:HGNC Symbol;Acc:HGNC:14677]","synonyms":"ZMYND5,SPN,NUDR","biotype":"protein_coding","ncbi_id":"10522","summary":"This gene encodes a zinc finger domain-containing protein that functions as a regulator of transcription. The encoded proteins binds to its own promoter as well as to that of several target genes. Activity of this protein is important in the regulation of embryonic development. Mutations in this gene have been found in individuals with autosomal dominant cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":644233,"end":706715,"strand":-1,"description":"DEAF1, transcription factor [Source:HGNC Symbol;Acc:HGNC:14677]"}, {"versioned_ensembl_gene_id":"ENSG00000111737.11","gene_symbol":"RAB35","gene_name":"RAB35, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9774]","synonyms":"H-ray","biotype":"protein_coding","ncbi_id":"11021","summary":null,"start":120095095,"end":120117502,"strand":-1,"description":"RAB35, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9774]"}, {"versioned_ensembl_gene_id":"ENSG00000274454.4","gene_symbol":"SLC22A18AS","gene_name":"solute carrier family 22 member 18 antisense [Source:HGNC Symbol;Acc:HGNC:10965]","synonyms":"BWSCR1B,BWR1B,SLC22A1LS,p27-BWR1B,ORCTL2S","biotype":"antisense_RNA","ncbi_id":"5003","summary":null,"start":2887804,"end":2903769,"strand":-1,"description":"solute carrier family 22 member 18 antisense [Source:HGNC Symbol;Acc:HGNC:10965]"}, {"versioned_ensembl_gene_id":"ENSG00000271252.1","gene_symbol":"AL683887.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95743096,"end":95759470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172037.13","gene_symbol":"LAMB2","gene_name":"laminin subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:6487]","synonyms":"NPHS5,LAMS","biotype":"protein_coding","ncbi_id":"3913","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins, composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively), form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the beta chain isoform laminin, beta 2. The beta 2 chain contains the 7 structural domains typical of beta chains of laminin, including the short alpha region. However, unlike beta 1 chain, beta 2 has a more restricted tissue distribution. It is enriched in the basement membrane of muscles at the neuromuscular junctions, kidney glomerulus and vascular smooth muscle. Transgenic mice in which the beta 2 chain gene was inactivated by homologous recombination, showed defects in the maturation of neuromuscular junctions and impairment of glomerular filtration. Alternative splicing involving a non consensus 5' splice site (gc) in the 5' UTR of this gene has been reported. It was suggested that inefficient splicing of this first intron, which does not change the protein sequence, results in a greater abundance of the unspliced form of the transcript than the spliced form. The full-length nature of the spliced transcript is not known. [provided by RefSeq, Aug 2011]","start":49121114,"end":49133118,"strand":-1,"description":"laminin subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:6487]"}, {"versioned_ensembl_gene_id":"ENSG00000280944.1","gene_symbol":"AC241851.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90365762,"end":90367722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182307.12","gene_symbol":"C8orf33","gene_name":"chromosome 8 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:26104]","synonyms":"FLJ20989","biotype":"protein_coding","ncbi_id":"65265","summary":null,"start":145052378,"end":145056030,"strand":1,"description":"chromosome 8 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:26104]"}, {"versioned_ensembl_gene_id":"ENSG00000272482.1","gene_symbol":"AC254633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12618900,"end":12619244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250629.1","gene_symbol":"AC091435.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38783580,"end":38792754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271195.1","gene_symbol":"AC018618.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61674767,"end":61675212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204021.3","gene_symbol":"LIPK","gene_name":"lipase family member K [Source:HGNC Symbol;Acc:HGNC:23444]","synonyms":"LIPL2,bA186O14.2","biotype":"protein_coding","ncbi_id":"643414","summary":null,"start":88724544,"end":88752786,"strand":1,"description":"lipase family member K [Source:HGNC Symbol;Acc:HGNC:23444]"}, {"versioned_ensembl_gene_id":"ENSG00000259345.5","gene_symbol":"AC013652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38865322,"end":39427195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233120.1","gene_symbol":"USP9YP15","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38751]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480713","summary":null,"start":18116527,"end":18117695,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38751]"}, {"versioned_ensembl_gene_id":"ENSG00000259423.2","gene_symbol":"AC113146.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39167739,"end":39180048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266288.1","gene_symbol":"AP005671.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5381641,"end":5385330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151023.16","gene_symbol":"ENKUR","gene_name":"enkurin, TRPC channel interacting protein [Source:HGNC Symbol;Acc:HGNC:28388]","synonyms":"MGC26778,enkurin,CFAP106,C10orf63","biotype":"protein_coding","ncbi_id":"219670","summary":"This gene encodes a protein that interacts with calmodulin and several transient receptor potential canonical cation channel proteins. The encoded protein may function as an adaptor to localize signal transduction machinery to calcium channels. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":24981979,"end":25062279,"strand":-1,"description":"enkurin, TRPC channel interacting protein [Source:HGNC Symbol;Acc:HGNC:28388]"}, {"versioned_ensembl_gene_id":"ENSG00000251073.1","gene_symbol":"NUDT19P5","gene_name":"nudix hydrolase 19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43589]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422445","summary":null,"start":158182825,"end":158183393,"strand":1,"description":"nudix hydrolase 19 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43589]"}, {"versioned_ensembl_gene_id":"ENSG00000248893.3","gene_symbol":"FAM138E","gene_name":"family with sequence similarity 138 member E [Source:HGNC Symbol;Acc:HGNC:32335]","synonyms":"F379","biotype":"lincRNA","ncbi_id":"100124412","summary":null,"start":101954885,"end":101956412,"strand":1,"description":"family with sequence similarity 138 member E [Source:HGNC Symbol;Acc:HGNC:32335]"}, {"versioned_ensembl_gene_id":"ENSG00000100077.14","gene_symbol":"GRK3","gene_name":"G protein-coupled receptor kinase 3 [Source:HGNC Symbol;Acc:HGNC:290]","synonyms":"BARK2,ADRBK2","biotype":"protein_coding","ncbi_id":"157","summary":"The beta-adrenergic receptor kinase specifically phosphorylates the agonist-occupied form of the beta-adrenergic and related G protein-coupled receptors. Overall, the beta adrenergic receptor kinase 2 has 85% amino acid similarity with beta adrenergic receptor kinase 1, with the protein kinase catalytic domain having 95% similarity. These data suggest the existence of a family of receptor kinases which may serve broadly to regulate receptor function. [provided by RefSeq, Jul 2008]","start":25564849,"end":25729294,"strand":1,"description":"G protein-coupled receptor kinase 3 [Source:HGNC Symbol;Acc:HGNC:290]"}, {"versioned_ensembl_gene_id":"ENSG00000102781.13","gene_symbol":"KATNAL1","gene_name":"katanin catalytic subunit A1 like 1 [Source:HGNC Symbol;Acc:HGNC:28361]","synonyms":"MGC2599","biotype":"protein_coding","ncbi_id":"84056","summary":null,"start":30202630,"end":30307484,"strand":-1,"description":"katanin catalytic subunit A1 like 1 [Source:HGNC Symbol;Acc:HGNC:28361]"}, {"versioned_ensembl_gene_id":"ENSG00000237387.1","gene_symbol":"AL022329.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25580241,"end":25581382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277936.4","gene_symbol":"MRPL45","gene_name":"mitochondrial ribosomal protein L45 [Source:HGNC Symbol;Acc:HGNC:16651]","synonyms":"MGC11321","biotype":"protein_coding","ncbi_id":"84311","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Alternative splicing results in multiple transcript variants. Pseudogenes corresponding to this gene are found on chromosomes 2p and 17q. [provided by RefSeq, May 2013]","start":38097522,"end":38123634,"strand":1,"description":"mitochondrial ribosomal protein L45 [Source:HGNC Symbol;Acc:HGNC:16651]"}, {"versioned_ensembl_gene_id":"ENSG00000259516.2","gene_symbol":"ANP32AP1","gene_name":"acidic nuclear phosphoprotein 32 family member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42949]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"723972","summary":null,"start":35181799,"end":35238197,"strand":1,"description":"acidic nuclear phosphoprotein 32 family member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42949]"}, {"versioned_ensembl_gene_id":"ENSG00000231974.6","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31691869,"end":31697663,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000259585.2","gene_symbol":"RBM17P4","gene_name":"RNA binding motif protein 17 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128974","summary":null,"start":35298249,"end":35299440,"strand":-1,"description":"RNA binding motif protein 17 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50369]"}, {"versioned_ensembl_gene_id":"ENSG00000282409.1","gene_symbol":"IGHJ1","gene_name":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28483","summary":null,"start":105866178,"end":105866229,"strand":-1,"description":"immunoglobulin heavy joining 1 [Source:HGNC Symbol;Acc:HGNC:5532]"}, {"versioned_ensembl_gene_id":"ENSG00000234088.1","gene_symbol":"RPS15AP7","gene_name":"ribosomal protein S15a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271142","summary":null,"start":62190522,"end":62190926,"strand":1,"description":"ribosomal protein S15a pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35648]"}, {"versioned_ensembl_gene_id":"ENSG00000183535.9","gene_symbol":"COL18A1-AS1","gene_name":"COL18A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23132]","synonyms":"PRED80,NCRNA00175,C21orf123","biotype":"antisense_RNA","ncbi_id":"378832","summary":null,"start":45419716,"end":45425070,"strand":-1,"description":"COL18A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23132]"}, {"versioned_ensembl_gene_id":"ENSG00000276272.1","gene_symbol":"AC024884.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56411944,"end":56413190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227511.1","gene_symbol":"AC005297.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26170052,"end":26170913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230402.2","gene_symbol":"LINC01349","gene_name":"long intergenic non-protein coding RNA 1349 [Source:HGNC Symbol;Acc:HGNC:50568]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128787","summary":null,"start":100627049,"end":100640613,"strand":-1,"description":"long intergenic non-protein coding RNA 1349 [Source:HGNC Symbol;Acc:HGNC:50568]"}, {"versioned_ensembl_gene_id":"ENSG00000266944.1","gene_symbol":"AC005262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3130717,"end":3131398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267327.1","gene_symbol":"AC009271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55893038,"end":56023522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206129.3","gene_symbol":"AC006305.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56003613,"end":56191262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226116.1","gene_symbol":"USP9YP6","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38078]","synonyms":"CDY24P","biotype":"unprocessed_pseudogene","ncbi_id":"100462820","summary":null,"start":17912699,"end":17921630,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38078]"}, {"versioned_ensembl_gene_id":"ENSG00000206338.9","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"P450c21B,CPS1,CYP21B,CAH1,CYP21,CA21H","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31850614,"end":31999312,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000270615.1","gene_symbol":"SGO1P1","gene_name":"shugoshin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50776]","synonyms":"SGOL1P1","biotype":"processed_pseudogene","ncbi_id":"100533666","summary":null,"start":69606855,"end":69608301,"strand":-1,"description":"shugoshin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50776]"}, {"versioned_ensembl_gene_id":"ENSG00000233106.1","gene_symbol":"RPL12P3","gene_name":"ribosomal protein L12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16335]","synonyms":"bA49G10.7","biotype":"processed_pseudogene","ncbi_id":"128862","summary":null,"start":33272262,"end":33272657,"strand":-1,"description":"ribosomal protein L12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16335]"}, {"versioned_ensembl_gene_id":"ENSG00000277193.1","gene_symbol":"GU182359.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54830865,"end":54845301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279034.1","gene_symbol":"AC011266.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40062903,"end":40066471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261715.1","gene_symbol":"LINC01477","gene_name":"long intergenic non-protein coding RNA 1477 [Source:HGNC Symbol;Acc:HGNC:51119]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927900","summary":null,"start":40066286,"end":40099233,"strand":1,"description":"long intergenic non-protein coding RNA 1477 [Source:HGNC Symbol;Acc:HGNC:51119]"}, {"versioned_ensembl_gene_id":"ENSG00000234744.1","gene_symbol":"USP9YP26","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:38762]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478929","summary":null,"start":26002254,"end":26008856,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:38762]"}, {"versioned_ensembl_gene_id":"ENSG00000138660.11","gene_symbol":"AP1AR","gene_name":"adaptor related protein complex 1 associated regulatory protein [Source:HGNC Symbol;Acc:HGNC:28808]","synonyms":"PRO0971,gamma-BAR,C4orf16,2C18","biotype":"protein_coding","ncbi_id":"55435","summary":null,"start":112231737,"end":112270047,"strand":1,"description":"adaptor related protein complex 1 associated regulatory protein [Source:HGNC Symbol;Acc:HGNC:28808]"}, {"versioned_ensembl_gene_id":"ENSG00000276498.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54802804,"end":54817417,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000182836.9","gene_symbol":"PLCXD3","gene_name":"phosphatidylinositol specific phospholipase C X domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31822]","synonyms":null,"biotype":"protein_coding","ncbi_id":"345557","summary":null,"start":41306954,"end":41510628,"strand":-1,"description":"phosphatidylinositol specific phospholipase C X domain containing 3 [Source:HGNC Symbol;Acc:HGNC:31822]"}, {"versioned_ensembl_gene_id":"ENSG00000226483.2","gene_symbol":"AL392088.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108508574,"end":108509243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227832.1","gene_symbol":"ST13P21","gene_name":"ST13, Hsp70 interacting protein pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642818","summary":null,"start":108502358,"end":108503455,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38864]"}, {"versioned_ensembl_gene_id":"ENSG00000283354.1","gene_symbol":"AL392088.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":108495475,"end":108501144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228930.1","gene_symbol":"MTCO1P3","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39604]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873205","summary":null,"start":45376191,"end":45376382,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39604]"}, {"versioned_ensembl_gene_id":"ENSG00000270535.1","gene_symbol":"ELOCP34","gene_name":"elongin C pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:49175]","synonyms":"TCEB1P34","biotype":"processed_pseudogene","ncbi_id":"106481671","summary":null,"start":25662900,"end":25663226,"strand":1,"description":"elongin C pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:49175]"}, {"versioned_ensembl_gene_id":"ENSG00000166634.6","gene_symbol":"SERPINB12","gene_name":"serpin family B member 12 [Source:HGNC Symbol;Acc:HGNC:14220]","synonyms":"YUKOPIN","biotype":"protein_coding","ncbi_id":"89777","summary":null,"start":63556160,"end":63567011,"strand":1,"description":"serpin family B member 12 [Source:HGNC Symbol;Acc:HGNC:14220]"}, {"versioned_ensembl_gene_id":"ENSG00000211794.3","gene_symbol":"TRAV12-3","gene_name":"T-cell receptor alpha variable 12-3 [Source:HGNC Symbol;Acc:HGNC:12107]","synonyms":"TRAV123,TCRAV2S2,TCRAV12S3","biotype":"TR_V_gene","ncbi_id":"28672","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21965451,"end":21966061,"strand":1,"description":"T-cell receptor alpha variable 12-3 [Source:HGNC Symbol;Acc:HGNC:12107]"}, {"versioned_ensembl_gene_id":"ENSG00000259659.1","gene_symbol":"AC009996.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44557829,"end":44559188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137038.7","gene_symbol":"DMAC1","gene_name":"distal membrane arm assembly complex 1 [Source:HGNC Symbol;Acc:HGNC:30536]","synonyms":"TMEM261,MGC4730,C9orf123","biotype":"protein_coding","ncbi_id":"90871","summary":null,"start":7796490,"end":7888380,"strand":-1,"description":"distal membrane arm assembly complex 1 [Source:HGNC Symbol;Acc:HGNC:30536]"}, {"versioned_ensembl_gene_id":"ENSG00000103197.16","gene_symbol":"TSC2","gene_name":"tuberous sclerosis 2 [Source:HGNC Symbol;Acc:HGNC:12363]","synonyms":"tuberin,TSC4,PPP1R160,LAM","biotype":"protein_coding","ncbi_id":"7249","summary":"Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":2047465,"end":2088720,"strand":1,"description":"tuberous sclerosis 2 [Source:HGNC Symbol;Acc:HGNC:12363]"}, {"versioned_ensembl_gene_id":"ENSG00000226063.1","gene_symbol":"AC009531.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35258381,"end":35259729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156172.5","gene_symbol":"C8orf37","gene_name":"chromosome 8 open reading frame 37 [Source:HGNC Symbol;Acc:HGNC:27232]","synonyms":"RP64,FLJ30600,CORD16,BBS21","biotype":"protein_coding","ncbi_id":"157657","summary":"This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]","start":95244919,"end":95269201,"strand":-1,"description":"chromosome 8 open reading frame 37 [Source:HGNC Symbol;Acc:HGNC:27232]"}, {"versioned_ensembl_gene_id":"ENSG00000188076.2","gene_symbol":"SCGB1C1","gene_name":"secretoglobin family 1C member 1 [Source:HGNC Symbol;Acc:HGNC:18394]","synonyms":"RYD5","biotype":"protein_coding","ncbi_id":"147199","summary":null,"start":193080,"end":194573,"strand":1,"description":"secretoglobin family 1C member 1 [Source:HGNC Symbol;Acc:HGNC:18394]"}, {"versioned_ensembl_gene_id":"ENSG00000173988.12","gene_symbol":"LRRC63","gene_name":"leucine rich repeat containing 63 [Source:HGNC Symbol;Acc:HGNC:34296]","synonyms":"RP11-139H14.4","biotype":"protein_coding","ncbi_id":"220416","summary":null,"start":46211943,"end":46277366,"strand":1,"description":"leucine rich repeat containing 63 [Source:HGNC Symbol;Acc:HGNC:34296]"}, {"versioned_ensembl_gene_id":"ENSG00000205810.8","gene_symbol":"KLRC3","gene_name":"killer cell lectin like receptor C3 [Source:HGNC Symbol;Acc:HGNC:6376]","synonyms":"NKG2-E","biotype":"protein_coding","ncbi_id":"3823","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. KLRC3 is a member of the NKG2 group which are expressed primarily in natural killer (NK) cells and encodes a family of transmembrane proteins characterized by a type II membrane orientation (extracellular C terminus) and the presence of a C-type lectin domain. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed on NK cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":10412312,"end":10420595,"strand":-1,"description":"killer cell lectin like receptor C3 [Source:HGNC Symbol;Acc:HGNC:6376]"}, {"versioned_ensembl_gene_id":"ENSG00000114302.15","gene_symbol":"PRKAR2A","gene_name":"protein kinase cAMP-dependent type II regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9391]","synonyms":"PRKAR2","biotype":"protein_coding","ncbi_id":"5576","summary":"cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. The protein encoded by this gene is one of the regulatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. It may interact with various A-kinase anchoring proteins and determine the subcellular localization of cAMP-dependent protein kinase. This subunit has been shown to regulate protein transport from endosomes to the Golgi apparatus and further to the endoplasmic reticulum (ER). [provided by RefSeq, Jul 2008]","start":48744597,"end":48847846,"strand":-1,"description":"protein kinase cAMP-dependent type II regulatory subunit alpha [Source:HGNC Symbol;Acc:HGNC:9391]"}, {"versioned_ensembl_gene_id":"ENSG00000139496.15","gene_symbol":"NUP58","gene_name":"nucleoporin 58 [Source:HGNC Symbol;Acc:HGNC:20261]","synonyms":"KIAA0410,NUPL1,NUP45","biotype":"protein_coding","ncbi_id":"9818","summary":"This gene encodes a member of the nucleoporin family that shares 87% sequence identity with rat nucleoporin p58. The protein is localized to the nuclear rim and is a component of the nuclear pore complex (NPC). All molecules entering or leaving the nucleus either diffuse through or are actively transported by the NPC. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":25301524,"end":25349800,"strand":1,"description":"nucleoporin 58 [Source:HGNC Symbol;Acc:HGNC:20261]"}, {"versioned_ensembl_gene_id":"ENSG00000280186.1","gene_symbol":"AL359258.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108200413,"end":108202743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223624.1","gene_symbol":"AL033528.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25888970,"end":25889109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229786.1","gene_symbol":"SNRPFP2","gene_name":"small nuclear ribonucleoprotein polypeptide F pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39665]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874411","summary":null,"start":25887360,"end":25887610,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide F pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39665]"}, {"versioned_ensembl_gene_id":"ENSG00000143079.14","gene_symbol":"CTTNBP2NL","gene_name":"CTTNBP2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:25330]","synonyms":"DKFZp547A023","biotype":"protein_coding","ncbi_id":"55917","summary":null,"start":112396181,"end":112463456,"strand":1,"description":"CTTNBP2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:25330]"}, {"versioned_ensembl_gene_id":"ENSG00000101868.10","gene_symbol":"POLA1","gene_name":"DNA polymerase alpha 1, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9173]","synonyms":"POLA,p180,NSX","biotype":"protein_coding","ncbi_id":"5422","summary":"This gene encodes the catalytic subunit of DNA polymerase, which together with a regulatory and two primase subunits, forms the DNA polymerase alpha complex. The catalytic subunit plays an essential role in the initiation of DNA replication. [provided by RefSeq, Mar 2010]","start":24693919,"end":24996986,"strand":1,"description":"DNA polymerase alpha 1, catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9173]"}, {"versioned_ensembl_gene_id":"ENSG00000185049.14","gene_symbol":"NELFA","gene_name":"negative elongation factor complex member A [Source:HGNC Symbol;Acc:HGNC:12768]","synonyms":"WHSC2,NELF-A","biotype":"protein_coding","ncbi_id":"7469","summary":"This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93% sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation. [provided by RefSeq, Jul 2008]","start":1982714,"end":2041903,"strand":-1,"description":"negative elongation factor complex member A [Source:HGNC Symbol;Acc:HGNC:12768]"}, {"versioned_ensembl_gene_id":"ENSG00000232472.1","gene_symbol":"EEF1B2P3","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3210]","synonyms":"EEF1B4","biotype":"processed_pseudogene","ncbi_id":"644820","summary":null,"start":24788392,"end":24789069,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3210]"}, {"versioned_ensembl_gene_id":"ENSG00000115904.12","gene_symbol":"SOS1","gene_name":"SOS Ras/Rac guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:11187]","synonyms":"HGF,GINGF,GF1","biotype":"protein_coding","ncbi_id":"6654","summary":"This gene encodes a protein that is a guanine nucleotide exchange factor for RAS proteins, membrane proteins that bind guanine nucleotides and participate in signal transduction pathways. GTP binding activates and GTP hydrolysis inactivates RAS proteins. The product of this gene may regulate RAS proteins by facilitating the exchange of GTP for GDP. Mutations in this gene are associated with gingival fibromatosis 1 and Noonan syndrome type 4. [provided by RefSeq, Jul 2008]","start":38981396,"end":39124345,"strand":-1,"description":"SOS Ras/Rac guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:11187]"}, {"versioned_ensembl_gene_id":"ENSG00000127589.4","gene_symbol":"TUBBP1","gene_name":"tubulin beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12414]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"92755","summary":null,"start":30351873,"end":30353518,"strand":1,"description":"tubulin beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12414]"}, {"versioned_ensembl_gene_id":"ENSG00000236428.10","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30668637,"end":30671637,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000253252.2","gene_symbol":"AC022784.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9180251,"end":9182519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282087.2","gene_symbol":"TBC1D3F","gene_name":"TBC1 domain family member 3F [Source:HGNC Symbol;Acc:HGNC:18257]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84218","summary":null,"start":36428990,"end":36439938,"strand":-1,"description":"TBC1 domain family member 3F [Source:HGNC Symbol;Acc:HGNC:18257]"}, {"versioned_ensembl_gene_id":"ENSG00000186191.7","gene_symbol":"BPIFB4","gene_name":"BPI fold containing family B member 4 [Source:HGNC Symbol;Acc:HGNC:16179]","synonyms":"dJ726C3.5,LPLUNC4,C20orf186","biotype":"protein_coding","ncbi_id":"149954","summary":null,"start":33079644,"end":33111751,"strand":1,"description":"BPI fold containing family B member 4 [Source:HGNC Symbol;Acc:HGNC:16179]"}, {"versioned_ensembl_gene_id":"ENSG00000243089.1","gene_symbol":"AC107029.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99507187,"end":99527113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237539.1","gene_symbol":"AC003669.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15646167,"end":15646875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214245.3","gene_symbol":"PUDPP3","gene_name":"pseudouridine 5'-phosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38118]","synonyms":"HDHD1P3,HDHD1DP","biotype":"processed_pseudogene","ncbi_id":"391242","summary":null,"start":33047517,"end":33048152,"strand":-1,"description":"pseudouridine 5'-phosphatase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38118]"}, {"versioned_ensembl_gene_id":"ENSG00000154447.14","gene_symbol":"SH3RF1","gene_name":"SH3 domain containing ring finger 1 [Source:HGNC Symbol;Acc:HGNC:17650]","synonyms":"SH3MD2,RNF142,POSH,KIAA1494","biotype":"protein_coding","ncbi_id":"57630","summary":"This gene encodes a protein containing an N-terminus RING-finger, four SH3 domains, and a region implicated in binding of the Rho GTPase Rac. Via the RING-finger, the encoded protein has been shown to function as an ubiquitin-protein ligase involved in protein sorting at the trans-Golgi network. The encoded protein may also act as a scaffold for the c-Jun N-terminal kinase signaling pathway, facilitating the formation of a functional signaling module. [provided by RefSeq, Jul 2008]","start":169094256,"end":169271105,"strand":-1,"description":"SH3 domain containing ring finger 1 [Source:HGNC Symbol;Acc:HGNC:17650]"}, {"versioned_ensembl_gene_id":"ENSG00000225833.1","gene_symbol":"GS1-594A7.3","gene_name":"uncharacterized LOC104798195 [Source:NCBI gene;Acc:104798195]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104798195","summary":null,"start":15602881,"end":15621484,"strand":1,"description":"uncharacterized LOC104798195 [Source:NCBI gene;Acc:104798195]"}, {"versioned_ensembl_gene_id":"ENSG00000203362.2","gene_symbol":"AL355802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43588230,"end":43591362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119946.10","gene_symbol":"CNNM1","gene_name":"cyclin and CBS domain divalent metal cation transport mediator 1 [Source:HGNC Symbol;Acc:HGNC:102]","synonyms":"ACDP1","biotype":"protein_coding","ncbi_id":"26507","summary":"This gene encodes a member of the ancient conserved domain protein family. The encoded protein may bind copper. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":99329099,"end":99394330,"strand":1,"description":"cyclin and CBS domain divalent metal cation transport mediator 1 [Source:HGNC Symbol;Acc:HGNC:102]"}, {"versioned_ensembl_gene_id":"ENSG00000223793.7","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32720520,"end":32726372,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000187109.13","gene_symbol":"NAP1L1","gene_name":"nucleosome assembly protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:7637]","synonyms":"MGC23410,NRP,NAP1L,NAP1,MGC8688","biotype":"protein_coding","ncbi_id":"4673","summary":"This gene encodes a member of the nucleosome assembly protein (NAP) family. This protein participates in DNA replication and may play a role in modulating chromatin formation and contribute to the regulation of cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms; however, not all have been fully described. [provided by RefSeq, Apr 2015]","start":76036587,"end":76085033,"strand":-1,"description":"nucleosome assembly protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:7637]"}, {"versioned_ensembl_gene_id":"ENSG00000281356.2","gene_symbol":"GOLGA8IP","gene_name":"golgin A8 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:26660]","synonyms":"GOLGA9P,GOLGA8I,FLJ35785","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"283796","summary":null,"start":22610118,"end":22620428,"strand":-1,"description":"golgin A8 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:26660]"}, {"versioned_ensembl_gene_id":"ENSG00000088827.12","gene_symbol":"SIGLEC1","gene_name":"sialic acid binding Ig like lectin 1 [Source:HGNC Symbol;Acc:HGNC:11127]","synonyms":"FLJ32150,FLJ00073,FLJ00055,FLJ00051,dJ1009E24.1,CD169,SN,SIGLEC-1,sialoadhesin","biotype":"protein_coding","ncbi_id":"6614","summary":"This gene encodes a member of the immunoglobulin superfamily. The encoded protein is a lectin-like adhesion molecule that binds glycoconjugate ligands on cell surfaces in a sialic acid-dependent manner. It is a type I transmembrane protein expressed only by a subpopulation of macrophages and is involved in mediating cell-cell interactions. Alternative splicing produces a transcript variant encoding an isoform that is soluble rather than membrane-bound; however, the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":3686970,"end":3707128,"strand":-1,"description":"sialic acid binding Ig like lectin 1 [Source:HGNC Symbol;Acc:HGNC:11127]"}, {"versioned_ensembl_gene_id":"ENSG00000130234.10","gene_symbol":"ACE2","gene_name":"angiotensin I converting enzyme 2 [Source:HGNC Symbol;Acc:HGNC:13557]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59272","summary":"The protein encoded by this gene belongs to the angiotensin-converting enzyme family of dipeptidyl carboxydipeptidases and has considerable homology to human angiotensin 1 converting enzyme. This secreted protein catalyzes the cleavage of angiotensin I into angiotensin 1-9, and angiotensin II into the vasodilator angiotensin 1-7. ACE2 is known to be expressed in various human organs, and its organ- and cell-specific expression suggests that it may play a role in the regulation of cardiovascular and renal function, as well as fertility. In addition, the encoded protein is a functional receptor for the spike glycoprotein of the human coronavirus HCoV-NL63 and the human severe acute respiratory syndrome coronaviruses, SARS-CoV and SARS-CoV-2, the latter is the causative agent of coronavirus disease-2019 (COVID-19). Multiple splice variants have been found for this gene and the dACE2 (or MIRb-ACE2) splice variant has been found to be interferon inducible. [provided by RefSeq, Nov 2020]","start":15561033,"end":15602148,"strand":-1,"description":"angiotensin I converting enzyme 2 [Source:HGNC Symbol;Acc:HGNC:13557]"}, {"versioned_ensembl_gene_id":"ENSG00000273177.1","gene_symbol":"AC092954.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168928169,"end":168928598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241383.1","gene_symbol":"LINC01997","gene_name":"long intergenic non-protein coding RNA 1997 [Source:HGNC Symbol;Acc:HGNC:52831]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374201","summary":null,"start":169003074,"end":169005466,"strand":1,"description":"long intergenic non-protein coding RNA 1997 [Source:HGNC Symbol;Acc:HGNC:52831]"}, {"versioned_ensembl_gene_id":"ENSG00000067798.14","gene_symbol":"NAV3","gene_name":"neuron navigator 3 [Source:HGNC Symbol;Acc:HGNC:15998]","synonyms":"POMFIL1,KIAA0938","biotype":"protein_coding","ncbi_id":"89795","summary":"This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]","start":77324641,"end":78213008,"strand":1,"description":"neuron navigator 3 [Source:HGNC Symbol;Acc:HGNC:15998]"}, {"versioned_ensembl_gene_id":"ENSG00000278937.1","gene_symbol":"AL137141.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46117864,"end":46122699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250580.1","gene_symbol":"SNRPCP8","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49823]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310851","summary":null,"start":130199708,"end":130199918,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49823]"}, {"versioned_ensembl_gene_id":"ENSG00000168065.15","gene_symbol":"SLC22A11","gene_name":"solute carrier family 22 member 11 [Source:HGNC Symbol;Acc:HGNC:18120]","synonyms":"OAT4","biotype":"protein_coding","ncbi_id":"55867","summary":"The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":64555626,"end":64572875,"strand":1,"description":"solute carrier family 22 member 11 [Source:HGNC Symbol;Acc:HGNC:18120]"}, {"versioned_ensembl_gene_id":"ENSG00000185189.17","gene_symbol":"NRBP2","gene_name":"nuclear receptor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19339]","synonyms":"DKFZp434P086","biotype":"protein_coding","ncbi_id":"340371","summary":null,"start":143833594,"end":143840974,"strand":-1,"description":"nuclear receptor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19339]"}, {"versioned_ensembl_gene_id":"ENSG00000275833.1","gene_symbol":"AC073107.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65764535,"end":65768306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223677.1","gene_symbol":"AL662791.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026680,"end":29027607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248607.1","gene_symbol":"AC117422.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126056923,"end":126058228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135829.16","gene_symbol":"DHX9","gene_name":"DExH-box helicase 9 [Source:HGNC Symbol;Acc:HGNC:2750]","synonyms":"RHA,LKP,DDX9","biotype":"protein_coding","ncbi_id":"1660","summary":"This gene encodes a member of the DEAH-containing family of RNA helicases. The encoded protein is an enzyme that catalyzes the ATP-dependent unwinding of double-stranded RNA and DNA-RNA complexes. This protein localizes to both the nucleus and the cytoplasm and functions as a transcriptional regulator. This protein may also be involved in the expression and nuclear export of retroviral RNAs. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 11 and 13.[provided by RefSeq, Feb 2010]","start":182839369,"end":182887751,"strand":1,"description":"DExH-box helicase 9 [Source:HGNC Symbol;Acc:HGNC:2750]"}, {"versioned_ensembl_gene_id":"ENSG00000205837.7","gene_symbol":"LINC00487","gene_name":"long intergenic non-protein coding RNA 487 [Source:HGNC Symbol;Acc:HGNC:42947]","synonyms":"FLJ42418","biotype":"lincRNA","ncbi_id":"400941","summary":null,"start":6728177,"end":6770311,"strand":-1,"description":"long intergenic non-protein coding RNA 487 [Source:HGNC Symbol;Acc:HGNC:42947]"}, {"versioned_ensembl_gene_id":"ENSG00000234012.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"Em:AB023051.5,NFBD1,KIAA0170","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30763719,"end":30781800,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000237645.1","gene_symbol":"AC092967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173644231,"end":173644711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266373.1","gene_symbol":"AP002472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3580169,"end":3580754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228838.1","gene_symbol":"AL355483.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53288024,"end":53289706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235352.1","gene_symbol":"AC023128.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144754776,"end":144755998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237473.1","gene_symbol":"AC068759.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173153737,"end":173336965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235911.1","gene_symbol":"AC019055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19711715,"end":19717576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224905.6","gene_symbol":"AP001347.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14027421,"end":14144468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269463.1","gene_symbol":"AP001160.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":62807682,"end":62808063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204176.13","gene_symbol":"SYT15","gene_name":"synaptotagmin 15 [Source:HGNC Symbol;Acc:HGNC:17167]","synonyms":"CHR10SYT","biotype":"protein_coding","ncbi_id":"83849","summary":"This gene encodes a member of the Synaptotagmin (Syt) family of membrane trafficking proteins. Members of this family contain a transmembrane region and a C-terminal-type tandem C2 domain. Unlike related family members, the encoded protein may be involved in membrane trafficking in non-neuronal tissues. Two trancript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":46578217,"end":46594173,"strand":1,"description":"synaptotagmin 15 [Source:HGNC Symbol;Acc:HGNC:17167]"}, {"versioned_ensembl_gene_id":"ENSG00000198276.15","gene_symbol":"UCKL1","gene_name":"uridine-cytidine kinase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:15938]","synonyms":"FLJ20517,URKL1","biotype":"protein_coding","ncbi_id":"54963","summary":"The protein encoded by this gene is a uridine kinase. Uridine kinases catalyze the phosphorylation of uridine to uridine monophosphate. This protein has been shown to bind to Epstein-Barr nuclear antigen 3 as well as natural killer lytic-associated molecule. Ubiquitination of this protein is enhanced by the presence of natural killer lytic-associated molecule. In addition, protein levels decrease in the presence of natural killer lytic-associated molecule, suggesting that association with natural killer lytic-associated molecule results in ubiquitination and subsequent degradation of this protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":63939829,"end":63956415,"strand":-1,"description":"uridine-cytidine kinase 1 like 1 [Source:HGNC Symbol;Acc:HGNC:15938]"}, {"versioned_ensembl_gene_id":"ENSG00000236818.1","gene_symbol":"ARL5AP2","gene_name":"ADP ribosylation factor like GTPase 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641380","summary":null,"start":99013103,"end":99013952,"strand":-1,"description":"ADP ribosylation factor like GTPase 5A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43937]"}, {"versioned_ensembl_gene_id":"ENSG00000196700.8","gene_symbol":"ZNF512B","gene_name":"zinc finger protein 512B [Source:HGNC Symbol;Acc:HGNC:29212]","synonyms":"MGC149845,GM632,MGC149846","biotype":"protein_coding","ncbi_id":"57473","summary":null,"start":63956702,"end":63969865,"strand":-1,"description":"zinc finger protein 512B [Source:HGNC Symbol;Acc:HGNC:29212]"}, {"versioned_ensembl_gene_id":"ENSG00000115307.16","gene_symbol":"AUP1","gene_name":"ancient ubiquitous protein 1 [Source:HGNC Symbol;Acc:HGNC:891]","synonyms":null,"biotype":"protein_coding","ncbi_id":"550","summary":"The protein encoded this gene is involved in several pathways including quality control of misfolded proteins in the endoplasmic reticulum and lipid droplet accumulation. Lipid droplets are organelles in the cytoplasm that store neutral lipids such as cholesterol esters and trigylycerides to prevent the overabundance of free cholesterol and fatty acids in cells, but also to act as storage for other metabolic processes, such as membrane biogenesis. Reduced expression of this gene results in reduced lipid droplet clustering, a function that is dependent on ubiquitination of the protein. This protein contains multiple domains including a hydrophobic N-terminal domain, an acetyltranferase domain, a ubiquitin-binding CUE domain, and a UBE2B2-binding domain (G2BR). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":74526645,"end":74529939,"strand":-1,"description":"ancient ubiquitous protein 1 [Source:HGNC Symbol;Acc:HGNC:891]"}, {"versioned_ensembl_gene_id":"ENSG00000107937.18","gene_symbol":"GTPBP4","gene_name":"GTP binding protein 4 [Source:HGNC Symbol;Acc:HGNC:21535]","synonyms":"NOG1,NGB,FLJ10690,FLJ10686,CRFG","biotype":"protein_coding","ncbi_id":"23560","summary":"GTP-binding proteins are GTPases and function as molecular switches that can flip between two states: active, when GTP is bound, and inactive, when GDP is bound. 'Active' in this context usually means that the molecule acts as a signal to trigger other events in the cell. When an extracellular ligand binds to a G-protein-linked receptor, the receptor changes its conformation and switches on the trimeric G proteins that associate with it by causing them to eject their GDP and replace it with GTP. The switch is turned off when the G protein hydrolyzes its own bound GTP, converting it back to GDP. But before that occurs, the active protein has an opportunity to diffuse away from the receptor and deliver its message for a prolonged period to its downstream target. [provided by RefSeq, Jul 2008]","start":988019,"end":1019936,"strand":1,"description":"GTP binding protein 4 [Source:HGNC Symbol;Acc:HGNC:21535]"}, {"versioned_ensembl_gene_id":"ENSG00000240429.1","gene_symbol":"LRRFIP1P1","gene_name":"LRR binding FLII interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101290506","summary":null,"start":179259028,"end":179261273,"strand":-1,"description":"LRR binding FLII interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32937]"}, {"versioned_ensembl_gene_id":"ENSG00000245870.3","gene_symbol":"LINC00682","gene_name":"long intergenic non-protein coding RNA 682 [Source:HGNC Symbol;Acc:HGNC:44466]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927074","summary":null,"start":41872747,"end":41882955,"strand":-1,"description":"long intergenic non-protein coding RNA 682 [Source:HGNC Symbol;Acc:HGNC:44466]"}, {"versioned_ensembl_gene_id":"ENSG00000229869.1","gene_symbol":"AL359878.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":933026,"end":942743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266513.1","gene_symbol":"AP002478.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3770017,"end":3771430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237713.1","gene_symbol":"AC011287.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13339201,"end":13365049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234073.1","gene_symbol":"AC011816.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36880184,"end":36880729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258239.1","gene_symbol":"MTND2P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42118]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873348","summary":null,"start":41698495,"end":41699182,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42118]"}, {"versioned_ensembl_gene_id":"ENSG00000133612.18","gene_symbol":"AGAP3","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:16923]","synonyms":"CENTG3","biotype":"protein_coding","ncbi_id":"116988","summary":"This gene encodes an essential component of the N-methyl-D-aspartate (NMDA) receptor signaling complex which mediates long-term potentiation in synapses by linking activation of NMDA receptor to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor trafficking. The encoded protein contains an N-terminal GTPase-like domain, a pleckstrin homology domain, an ArfGAP domain and several C-terminal ankryn repeat domains. [provided by RefSeq, Apr 2017]","start":151085831,"end":151144436,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:16923]"}, {"versioned_ensembl_gene_id":"ENSG00000215252.11","gene_symbol":"GOLGA8B","gene_name":"golgin A8 family member B [Source:HGNC Symbol;Acc:HGNC:31973]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440270","summary":null,"start":34525207,"end":34588503,"strand":-1,"description":"golgin A8 family member B [Source:HGNC Symbol;Acc:HGNC:31973]"}, {"versioned_ensembl_gene_id":"ENSG00000279061.1","gene_symbol":"Z98043.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":172752586,"end":172752924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235001.3","gene_symbol":"EIF4A1P2","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359792","summary":null,"start":5337745,"end":5338964,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23946]"}, {"versioned_ensembl_gene_id":"ENSG00000078070.12","gene_symbol":"MCCC1","gene_name":"methylcrotonoyl-CoA carboxylase 1 [Source:HGNC Symbol;Acc:HGNC:6936]","synonyms":"MCCA","biotype":"protein_coding","ncbi_id":"56922","summary":"This gene encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. [provided by RefSeq, Jul 2008]","start":183015218,"end":183116075,"strand":-1,"description":"methylcrotonoyl-CoA carboxylase 1 [Source:HGNC Symbol;Acc:HGNC:6936]"}, {"versioned_ensembl_gene_id":"ENSG00000257570.1","gene_symbol":"AC020612.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49709237,"end":49709336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259818.1","gene_symbol":"AL606760.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53220663,"end":53224253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162669.15","gene_symbol":"HFM1","gene_name":"HFM1, ATP dependent DNA helicase homolog [Source:HGNC Symbol;Acc:HGNC:20193]","synonyms":"FLJ39011,FLJ36760,SEC63D1,MER3","biotype":"protein_coding","ncbi_id":"164045","summary":"The protein encoded by this gene is thought to be an ATP-dependent DNA helicase and is expressed mainly in germ-line cells. Defects in this gene are a cause of premature ovarian failure 9 (POF9). [provided by RefSeq, Apr 2014]","start":91260766,"end":91404869,"strand":-1,"description":"HFM1, ATP dependent DNA helicase homolog [Source:HGNC Symbol;Acc:HGNC:20193]"}, {"versioned_ensembl_gene_id":"ENSG00000283973.1","gene_symbol":"AC099795.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42959065,"end":42961864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213295.3","gene_symbol":"AC092106.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106247369,"end":106247741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255508.7","gene_symbol":"AP002990.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":62559603,"end":62591531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229927.2","gene_symbol":"RHEBP1","gene_name":"Ras-homolog enriched in brain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10010]","synonyms":"RHEB1,RHEB","biotype":"processed_pseudogene","ncbi_id":"6008","summary":null,"start":46634911,"end":46635466,"strand":-1,"description":"Ras-homolog enriched in brain pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10010]"}, {"versioned_ensembl_gene_id":"ENSG00000165609.12","gene_symbol":"NUDT5","gene_name":"nudix hydrolase 5 [Source:HGNC Symbol;Acc:HGNC:8052]","synonyms":"YSA1H,hYSAH1","biotype":"protein_coding","ncbi_id":"11164","summary":"This gene belongs to the Nudix (nucleoside diphosphate linked moiety X) hydrolase superfamily. The encoded enzyme catalyzes the hydrolysis of modified nucleoside diphosphates, including ADP-ribose (ADPR) and 8-oxoGua-containing 8-oxo-dADP and 8-oxo-dGDP. Protein-bound ADP ribose can be hazardous to the cell because it can modify some amino acid residues, resulting in the inhibition of ATP-activated potassium channels. 8-oxoGua is an oxidized form of guanine that can potentially alter genetic information by pairing with adenine and cytosine in RNA. Presence of 8-oxoGua in RNA results in formation of abnormal proteins due to translational errors. [provided by RefSeq, Aug 2013]","start":12165325,"end":12196144,"strand":-1,"description":"nudix hydrolase 5 [Source:HGNC Symbol;Acc:HGNC:8052]"}, {"versioned_ensembl_gene_id":"ENSG00000171495.16","gene_symbol":"MROH2B","gene_name":"maestro heat like repeat family member 2B [Source:HGNC Symbol;Acc:HGNC:26857]","synonyms":"HEATR7B2,FLJ40243,DKFZp781F0822","biotype":"protein_coding","ncbi_id":"133558","summary":null,"start":40998017,"end":41071342,"strand":-1,"description":"maestro heat like repeat family member 2B [Source:HGNC Symbol;Acc:HGNC:26857]"}, {"versioned_ensembl_gene_id":"ENSG00000275512.1","gene_symbol":"AC007998.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35403996,"end":35406528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206329.15","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32111042,"end":32121288,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000217330.1","gene_symbol":"SSXP10","gene_name":"SSX family pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:30638]","synonyms":"psiSSX10","biotype":"processed_pseudogene","ncbi_id":"100287603","summary":null,"start":118589070,"end":118589634,"strand":1,"description":"SSX family pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:30638]"}, {"versioned_ensembl_gene_id":"ENSG00000249013.1","gene_symbol":"FTH1P21","gene_name":"ferritin heavy chain 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:3997]","synonyms":"FTHP2,FTHL21","biotype":"processed_pseudogene","ncbi_id":"2510","summary":null,"start":156006478,"end":156006988,"strand":1,"description":"ferritin heavy chain 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:3997]"}, {"versioned_ensembl_gene_id":"ENSG00000256553.1","gene_symbol":"TRAV1-2","gene_name":"T-cell receptor alpha variable 1-2 [Source:HGNC Symbol;Acc:HGNC:12102]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28692","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21642889,"end":21643578,"strand":1,"description":"T-cell receptor alpha variable 1-2 [Source:HGNC Symbol;Acc:HGNC:12102]"}, {"versioned_ensembl_gene_id":"ENSG00000120889.12","gene_symbol":"TNFRSF10B","gene_name":"TNF receptor superfamily member 10b [Source:HGNC Symbol;Acc:HGNC:11905]","synonyms":"CD262,TRICKB,TRICK2A,TRAIL-R2,KILLER,DR5","biotype":"protein_coding","ncbi_id":"8795","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily, and contains an intracellular death domain. This receptor can be activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL/APO-2L), and transduces an apoptosis signal. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. Two transcript variants encoding different isoforms and one non-coding transcript have been found for this gene. [provided by RefSeq, Mar 2009]","start":23020133,"end":23069179,"strand":-1,"description":"TNF receptor superfamily member 10b [Source:HGNC Symbol;Acc:HGNC:11905]"}, {"versioned_ensembl_gene_id":"ENSG00000261428.2","gene_symbol":"AC097461.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":222566899,"end":222569719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255569.1","gene_symbol":"TRAV1-1","gene_name":"T-cell receptor alpha variable 1-1 [Source:HGNC Symbol;Acc:HGNC:12101]","synonyms":"TRAV11,TCRAV7S1,TCRAV1S1","biotype":"TR_V_gene","ncbi_id":"28693","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21621838,"end":21622567,"strand":1,"description":"T-cell receptor alpha variable 1-1 [Source:HGNC Symbol;Acc:HGNC:12101]"}, {"versioned_ensembl_gene_id":"ENSG00000262008.1","gene_symbol":"AC010547.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71443055,"end":71443856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234985.2","gene_symbol":"AC074085.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121440834,"end":121441261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283058.1","gene_symbol":"AC009234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50620963,"end":50632993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233411.1","gene_symbol":"AL359962.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":167457383,"end":167458661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231945.8","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31768274,"end":31785735,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000273160.1","gene_symbol":"AL359962.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167457742,"end":167459891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229518.1","gene_symbol":"UBE2V1P3","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23983]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359798","summary":null,"start":3866306,"end":3866722,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23983]"}, {"versioned_ensembl_gene_id":"ENSG00000100296.13","gene_symbol":"THOC5","gene_name":"THO complex 5 [Source:HGNC Symbol;Acc:HGNC:19074]","synonyms":"PK1.3,KIAA0983,fSAP79,Fmip,C22orf19","biotype":"protein_coding","ncbi_id":"8563","summary":null,"start":29505879,"end":29555216,"strand":-1,"description":"THO complex 5 [Source:HGNC Symbol;Acc:HGNC:19074]"}, {"versioned_ensembl_gene_id":"ENSG00000249380.1","gene_symbol":"AC138853.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34373028,"end":34373850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179750.15","gene_symbol":"APOBEC3B","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3B [Source:HGNC Symbol;Acc:HGNC:17352]","synonyms":"PHRBNL,FLJ21201","biotype":"protein_coding","ncbi_id":"9582","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. A hybrid gene results from the deletion of approximately 29.5 kb of sequence between this gene, APOBEC3B, and the adjacent gene APOBEC3A. The breakpoints of the deletion are within the two genes, so the deletion allele is predicted to have the promoter and coding region of APOBEC3A, but the 3' UTR of APOBEC3B. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]","start":38982347,"end":38992804,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3B [Source:HGNC Symbol;Acc:HGNC:17352]"}, {"versioned_ensembl_gene_id":"ENSG00000249310.2","gene_symbol":"APOBEC3B-AS1","gene_name":"APOBEC3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43836]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874530","summary":null,"start":38991559,"end":38998209,"strand":-1,"description":"APOBEC3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43836]"}, {"versioned_ensembl_gene_id":"ENSG00000227686.7","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31781844,"end":31786187,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000175203.15","gene_symbol":"DCTN2","gene_name":"dynactin subunit 2 [Source:HGNC Symbol;Acc:HGNC:2712]","synonyms":"RBP50,DCTN-50","biotype":"protein_coding","ncbi_id":"10540","summary":"This gene encodes a 50-kD subunit of dynactin, a macromolecular complex consisting of 10-11 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit is present in 4-5 copies per dynactin molecule. It contains three short alpha-helical coiled-coil domains that may mediate association with self or other dynactin subunits. It may interact directly with the largest subunit (p150) of dynactin and may affix p150 in place. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":57530102,"end":57547331,"strand":-1,"description":"dynactin subunit 2 [Source:HGNC Symbol;Acc:HGNC:2712]"}, {"versioned_ensembl_gene_id":"ENSG00000231074.8","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ25550,Em:AB014087.1,FLJ31598","biotype":"antisense_RNA","ncbi_id":"414777","summary":null,"start":30287397,"end":30327150,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000226527.1","gene_symbol":"AP000289.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33111699,"end":33123703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278414.5","gene_symbol":"GU182357.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771198,"end":54780682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233862.5","gene_symbol":"AC016907.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30051066,"end":30143804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225943.1","gene_symbol":"AC016907.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30077093,"end":30078272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203855.7","gene_symbol":"HSD3BP4","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:5222]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"128102","summary":null,"start":119564066,"end":119572067,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:5222]"}, {"versioned_ensembl_gene_id":"ENSG00000237556.1","gene_symbol":"KCND3-AS1","gene_name":"KCND3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40317]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873995","summary":null,"start":111909336,"end":111910931,"strand":1,"description":"KCND3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40317]"}, {"versioned_ensembl_gene_id":"ENSG00000008323.15","gene_symbol":"PLEKHG6","gene_name":"pleckstrin homology and RhoGEF domain containing G6 [Source:HGNC Symbol;Acc:HGNC:25562]","synonyms":"FLJ10665,MYOGEF","biotype":"protein_coding","ncbi_id":"55200","summary":null,"start":6310436,"end":6328506,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G6 [Source:HGNC Symbol;Acc:HGNC:25562]"}, {"versioned_ensembl_gene_id":"ENSG00000225653.1","gene_symbol":"RNF19BPY","gene_name":"ring finger protein 19B pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:38398]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419722","summary":null,"start":3777997,"end":3779546,"strand":-1,"description":"ring finger protein 19B pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:38398]"}, {"versioned_ensembl_gene_id":"ENSG00000275064.1","gene_symbol":"AC239860.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":145509047,"end":145520594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232490.6","gene_symbol":"OSBPL10-AS1","gene_name":"OSBPL10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40767]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874206","summary":null,"start":31704058,"end":31721652,"strand":1,"description":"OSBPL10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40767]"}, {"versioned_ensembl_gene_id":"ENSG00000147324.10","gene_symbol":"MFHAS1","gene_name":"malignant fibrous histiocytoma amplified sequence 1 [Source:HGNC Symbol;Acc:HGNC:16982]","synonyms":"ROCO4,MASL1,LRRC65","biotype":"protein_coding","ncbi_id":"9258","summary":"Identified in a human 8p amplicon, this gene is a potential oncogene whose expression is enhanced in some malignant fibrous histiocytomas (MFH). The primary structure of its product includes an ATP/GTP-binding site, three leucine zipper domains, and a leucine-rich tandem repeat, which are structural or functional elements for interactions among proteins related to the cell cycle, and which suggest that overexpression might be oncogenic with respect to MFH. [provided by RefSeq, Jul 2008]","start":8783354,"end":8893645,"strand":-1,"description":"malignant fibrous histiocytoma amplified sequence 1 [Source:HGNC Symbol;Acc:HGNC:16982]"}, {"versioned_ensembl_gene_id":"ENSG00000244268.1","gene_symbol":"AC117394.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153156511,"end":153161775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261728.1","gene_symbol":"AL138690.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34925834,"end":34928076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075151.20","gene_symbol":"EIF4G3","gene_name":"eukaryotic translation initiation factor 4 gamma 3 [Source:HGNC Symbol;Acc:HGNC:3298]","synonyms":"eIF4GII","biotype":"protein_coding","ncbi_id":"8672","summary":"The protein encoded by this gene is thought to be part of the eIF4F protein complex, which is involved in mRNA cap recognition and transport of mRNAs to the ribosome. Interestingly, a microRNA (miR-520c-3p) has been found that negatively regulates synthesis of the encoded protein, and this leads to a global decrease in protein translation and cell proliferation. Therefore, this protein is a key component of the anti-tumor activity of miR-520c-3p. [provided by RefSeq, May 2016]","start":20806292,"end":21176888,"strand":-1,"description":"eukaryotic translation initiation factor 4 gamma 3 [Source:HGNC Symbol;Acc:HGNC:3298]"}, {"versioned_ensembl_gene_id":"ENSG00000231081.1","gene_symbol":"AL078587.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26008791,"end":26010531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254367.5","gene_symbol":"AC087269.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8723693,"end":8782479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233036.1","gene_symbol":"KRTAP8-2P","gene_name":"keratin associated protein 8-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:18948]","synonyms":"KRTAP8P1,KAP8A","biotype":"unprocessed_pseudogene","ncbi_id":"337980","summary":null,"start":30802242,"end":30802427,"strand":-1,"description":"keratin associated protein 8-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:18948]"}, {"versioned_ensembl_gene_id":"ENSG00000155754.14","gene_symbol":"C2CD6","gene_name":"C2 calcium dependent domain containing 6 [Source:HGNC Symbol;Acc:HGNC:14438]","synonyms":"FLJ25351,ALS2CR11","biotype":"protein_coding","ncbi_id":"151254","summary":"An autosomal recessive form of juvenile amyotrophic lateral sclerosis was originally mapped to a region of chromosome 2 that includes this gene. The encoded protein contains a calcium-dependent membrane targeting C2 domain. This domain is often found in proteins that are involved in membrane trafficking and signal transduction. [provided by RefSeq, Jun 2016]","start":201487425,"end":201619178,"strand":-1,"description":"C2 calcium dependent domain containing 6 [Source:HGNC Symbol;Acc:HGNC:14438]"}, {"versioned_ensembl_gene_id":"ENSG00000234282.1","gene_symbol":"AL109809.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1722045,"end":1722537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162231.13","gene_symbol":"NXF1","gene_name":"nuclear RNA export factor 1 [Source:HGNC Symbol;Acc:HGNC:8071]","synonyms":"TAP,Mex67,DKFZp667O0311","biotype":"protein_coding","ncbi_id":"10482","summary":"This gene is one member of a family of nuclear RNA export factor genes. Common domain features of this family are a noncanonical RNP-type RNA-binding domain (RBD), 4 leucine-rich repeats (LRRs), a nuclear transport factor 2 (NTF2)-like domain that allows heterodimerization with NTF2-related export protein-1 (NXT1), and a ubiquitin-associated domain that mediates interactions with nucleoporins. The LRRs and NTF2-like domains are required for export activity. Alternative splicing seems to be a common mechanism in this gene family. The encoded protein of this gene shuttles between the nucleus and the cytoplasm and binds in vivo to poly(A)+ RNA. It is the vertebrate homologue of the yeast protein Mex67p. The encoded protein overcomes the mRNA export block caused by the presence of saturating amounts of CTE (constitutive transport element) RNA of type D retroviruses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":62792123,"end":62806302,"strand":-1,"description":"nuclear RNA export factor 1 [Source:HGNC Symbol;Acc:HGNC:8071]"}, {"versioned_ensembl_gene_id":"ENSG00000269752.1","gene_symbol":"AC008761.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17613722,"end":17614430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279300.1","gene_symbol":"AC008761.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17622447,"end":17623338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169855.19","gene_symbol":"ROBO1","gene_name":"roundabout guidance receptor 1 [Source:HGNC Symbol;Acc:HGNC:10249]","synonyms":"SAX3,FLJ21882,DUTT1","biotype":"protein_coding","ncbi_id":"6091","summary":"Bilateral symmetric nervous systems have special midline structures that establish a partition between the two mirror image halves. Some axons project toward and across the midline in response to long-range chemoattractants emanating from the midline. The product of this gene is a member of the immunoglobulin gene superfamily and encodes an integral membrane protein that functions in axon guidance and neuronal precursor cell migration. This receptor is activated by SLIT-family proteins, resulting in a repulsive effect on glioma cell guidance in the developing brain. A related gene is located at an adjacent region on chromosome 3. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":78597240,"end":79767815,"strand":-1,"description":"roundabout guidance receptor 1 [Source:HGNC Symbol;Acc:HGNC:10249]"}, {"versioned_ensembl_gene_id":"ENSG00000270035.1","gene_symbol":"AL359881.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7698303,"end":7698872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225126.1","gene_symbol":"AL365194.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7441096,"end":7441554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187026.2","gene_symbol":"KRTAP21-2","gene_name":"keratin associated protein 21-2 [Source:HGNC Symbol;Acc:HGNC:18946]","synonyms":"KAP21.2","biotype":"protein_coding","ncbi_id":"337978","summary":null,"start":30746794,"end":30747233,"strand":-1,"description":"keratin associated protein 21-2 [Source:HGNC Symbol;Acc:HGNC:18946]"}, {"versioned_ensembl_gene_id":"ENSG00000236400.1","gene_symbol":"KRTAP21-4P","gene_name":"keratin associated protein 21-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18954]","synonyms":"KRTAP21P1,KAP21A","biotype":"unprocessed_pseudogene","ncbi_id":"337986","summary":null,"start":30741780,"end":30742595,"strand":-1,"description":"keratin associated protein 21-4, pseudogene [Source:HGNC Symbol;Acc:HGNC:18954]"}, {"versioned_ensembl_gene_id":"ENSG00000261067.7","gene_symbol":"AC109460.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28974804,"end":28990775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116729.13","gene_symbol":"WLS","gene_name":"wntless Wnt ligand secretion mediator [Source:HGNC Symbol;Acc:HGNC:30238]","synonyms":"wls,MRP,mig-14,GPR177,FLJ23091,EVI,C1orf139","biotype":"protein_coding","ncbi_id":"79971","summary":null,"start":68098473,"end":68233120,"strand":-1,"description":"wntless Wnt ligand secretion mediator [Source:HGNC Symbol;Acc:HGNC:30238]"}, {"versioned_ensembl_gene_id":"ENSG00000101327.8","gene_symbol":"PDYN","gene_name":"prodynorphin [Source:HGNC Symbol;Acc:HGNC:8820]","synonyms":"ADCA,SCA23,PENKB","biotype":"protein_coding","ncbi_id":"5173","summary":"The protein encoded by this gene is a preproprotein that is proteolytically processed to form the secreted opioid peptides beta-neoendorphin, dynorphin, leu-enkephalin, rimorphin, and leumorphin. These peptides are ligands for the kappa-type of opioid receptor. Dynorphin is involved in modulating responses to several psychoactive substances, including cocaine. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]","start":1978757,"end":1994285,"strand":-1,"description":"prodynorphin [Source:HGNC Symbol;Acc:HGNC:8820]"}, {"versioned_ensembl_gene_id":"ENSG00000130477.15","gene_symbol":"UNC13A","gene_name":"unc-13 homolog A [Source:HGNC Symbol;Acc:HGNC:23150]","synonyms":"Munc13-1,KIAA1032","biotype":"protein_coding","ncbi_id":"23025","summary":"This gene encodes a member of the UNC13 family. UNC13 proteins bind to phorbol esters and diacylglycerol and play important roles in neurotransmitter release at synapses. Single nucleotide polymorphisms in this gene may be associated with sporadic amyotrophic lateral sclerosis. [provided by RefSeq, Feb 2012]","start":17601328,"end":17688365,"strand":-1,"description":"unc-13 homolog A [Source:HGNC Symbol;Acc:HGNC:23150]"}, {"versioned_ensembl_gene_id":"ENSG00000130147.15","gene_symbol":"SH3BP4","gene_name":"SH3 domain binding protein 4 [Source:HGNC Symbol;Acc:HGNC:10826]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23677","summary":"This gene encodes a protein with 3 Asn-Pro-Phe (NPF) motifs, an SH3 domain, a PXXP motif, a bipartite nuclear targeting signal, and a tyrosine phosphorylation site. This protein is involved in cargo-specific control of clathrin-mediated endocytosis, specifically controlling the internalization of a specific protein receptor. [provided by RefSeq, Jul 2008]","start":234951973,"end":235055714,"strand":1,"description":"SH3 domain binding protein 4 [Source:HGNC Symbol;Acc:HGNC:10826]"}, {"versioned_ensembl_gene_id":"ENSG00000248461.1","gene_symbol":"LINC02119","gene_name":"long intergenic non-protein coding RNA 2119 [Source:HGNC Symbol;Acc:HGNC:52975]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929745","summary":null,"start":38148480,"end":38153715,"strand":1,"description":"long intergenic non-protein coding RNA 2119 [Source:HGNC Symbol;Acc:HGNC:52975]"}, {"versioned_ensembl_gene_id":"ENSG00000217929.4","gene_symbol":"CICP18","gene_name":"capicua transcriptional repressor pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:48828]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"646070","summary":null,"start":131910,"end":145083,"strand":-1,"description":"capicua transcriptional repressor pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:48828]"}, {"versioned_ensembl_gene_id":"ENSG00000260331.1","gene_symbol":"AC079148.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18547386,"end":18548204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235602.5","gene_symbol":"POU5F1P3","gene_name":"POU class 5 homeobox 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9222]","synonyms":"POU5FLC12,POU5F1L,OTF3L","biotype":"processed_pseudogene","ncbi_id":"642559","summary":null,"start":8133772,"end":8134849,"strand":-1,"description":"POU class 5 homeobox 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9222]"}, {"versioned_ensembl_gene_id":"ENSG00000099910.16","gene_symbol":"KLHL22","gene_name":"kelch like family member 22 [Source:HGNC Symbol;Acc:HGNC:25888]","synonyms":"KELCHL,FLJ14360","biotype":"protein_coding","ncbi_id":"84861","summary":null,"start":20441519,"end":20495883,"strand":-1,"description":"kelch like family member 22 [Source:HGNC Symbol;Acc:HGNC:25888]"}, {"versioned_ensembl_gene_id":"ENSG00000277867.1","gene_symbol":"AC138649.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22714939,"end":22715225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173699.15","gene_symbol":"SPATA3","gene_name":"spermatogenesis associated 3 [Source:HGNC Symbol;Acc:HGNC:17884]","synonyms":"TSARG1","biotype":"protein_coding","ncbi_id":"130560","summary":null,"start":230996121,"end":231025055,"strand":1,"description":"spermatogenesis associated 3 [Source:HGNC Symbol;Acc:HGNC:17884]"}, {"versioned_ensembl_gene_id":"ENSG00000275342.4","gene_symbol":"PRAG1","gene_name":"PEAK1 related kinase activating pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:25438]","synonyms":"NACK,DKFZp761P0423,SgK223,PRAGMIN,PEAK2","biotype":"protein_coding","ncbi_id":"157285","summary":"This gene encodes an enzyme that belongs to the tyrosine protein kinase family. A similar protein in rat binds to Rho family GTPase 2 (Rnd2) and regulates neurite outgrowth via activation of Ras homolog gene family, member A (RhoA). [provided by RefSeq, Mar 2014]","start":8317736,"end":8386498,"strand":-1,"description":"PEAK1 related kinase activating pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:25438]"}, {"versioned_ensembl_gene_id":"ENSG00000260107.1","gene_symbol":"AC005606.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1997654,"end":1998374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269210.2","gene_symbol":"AC019171.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38959287,"end":38960342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250659.2","gene_symbol":"AP001363.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62537312,"end":62542018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249111.1","gene_symbol":"AC108517.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59152834,"end":59176146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250973.1","gene_symbol":"KRTAP13-6P","gene_name":"keratin associated protein 13-6, pseudogene [Source:HGNC Symbol;Acc:HGNC:18930]","synonyms":"KRTAP13P2,KAP13B","biotype":"unprocessed_pseudogene","ncbi_id":"337965","summary":null,"start":30356515,"end":30356885,"strand":-1,"description":"keratin associated protein 13-6, pseudogene [Source:HGNC Symbol;Acc:HGNC:18930]"}, {"versioned_ensembl_gene_id":"ENSG00000198053.11","gene_symbol":"SIRPA","gene_name":"signal regulatory protein alpha [Source:HGNC Symbol;Acc:HGNC:9662]","synonyms":"SIRPalpha2,SIRPalpha,SIRP-ALPHA-1,SIRP,SHPS1,SHPS-1,PTPNS1,P84,MYD-1,MFR,CD172a,BIT","biotype":"protein_coding","ncbi_id":"140885","summary":"The protein encoded by this gene is a member of the signal-regulatory-protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. This protein can be phosphorylated by tyrosine kinases. The phospho-tyrosine residues of this PTP have been shown to recruit SH2 domain containing tyrosine phosphatases (PTP), and serve as substrates of PTPs. This protein was found to participate in signal transduction mediated by various growth factor receptors. CD47 has been demonstrated to be a ligand for this receptor protein. This gene and its product share very high similarity with several other members of the SIRP family. These related genes are located in close proximity to each other on chromosome 20p13. Multiple alternatively spliced transcript variants have been determined for this gene. [provided by RefSeq, Jul 2008]","start":1894167,"end":1940592,"strand":1,"description":"signal regulatory protein alpha [Source:HGNC Symbol;Acc:HGNC:9662]"}, {"versioned_ensembl_gene_id":"ENSG00000104833.11","gene_symbol":"TUBB4A","gene_name":"tubulin beta 4A class IVa [Source:HGNC Symbol;Acc:HGNC:20774]","synonyms":"TUBB4,DYT4,beta-5","biotype":"protein_coding","ncbi_id":"10382","summary":"This gene encodes a member of the beta tubulin family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. Mutations in this gene cause hypomyelinating leukodystrophy-6 and autosomal dominant torsion dystonia-4. Alternate splicing results in multiple transcript variants encoding different isoforms. A pseudogene of this gene is found on chromosome X. [provided by RefSeq, Jan 2014]","start":6494319,"end":6502848,"strand":-1,"description":"tubulin beta 4A class IVa [Source:HGNC Symbol;Acc:HGNC:20774]"}, {"versioned_ensembl_gene_id":"ENSG00000114547.9","gene_symbol":"ROPN1B","gene_name":"rhophilin associated tail protein 1B [Source:HGNC Symbol;Acc:HGNC:31927]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152015","summary":null,"start":125969144,"end":125983454,"strand":1,"description":"rhophilin associated tail protein 1B [Source:HGNC Symbol;Acc:HGNC:31927]"}, {"versioned_ensembl_gene_id":"ENSG00000227874.1","gene_symbol":"GRAMD4P1","gene_name":"GRAM domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39653]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631252","summary":null,"start":13665868,"end":13667546,"strand":-1,"description":"GRAM domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39653]"}, {"versioned_ensembl_gene_id":"ENSG00000280048.1","gene_symbol":"AC012409.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96112628,"end":96116051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236924.1","gene_symbol":"AL162411.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6645956,"end":6670635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167962.13","gene_symbol":"ZNF598","gene_name":"zinc finger protein 598 [Source:HGNC Symbol;Acc:HGNC:28079]","synonyms":"FLJ00086","biotype":"protein_coding","ncbi_id":"90850","summary":"Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This protein and Grb10-interacting GYF protein 2 have been identified as a components of the mammalian 4EHP (m4EHP) complex. The complex is thought to function as a translation repressor in embryonic development. [provided by RefSeq, Oct 2012]","start":1997654,"end":2009823,"strand":-1,"description":"zinc finger protein 598 [Source:HGNC Symbol;Acc:HGNC:28079]"}, {"versioned_ensembl_gene_id":"ENSG00000267047.1","gene_symbol":"AC040977.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6985494,"end":7019414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263316.1","gene_symbol":"AC027763.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6954098,"end":6978960,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248593.3","gene_symbol":"DSTNP2","gene_name":"destrin, actin depolymerizing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34546]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"171220","summary":null,"start":6884682,"end":6885786,"strand":1,"description":"destrin, actin depolymerizing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34546]"}, {"versioned_ensembl_gene_id":"ENSG00000275852.1","gene_symbol":"LINC01742","gene_name":"long intergenic non-protein coding RNA 1742 [Source:HGNC Symbol;Acc:HGNC:52530]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376992","summary":null,"start":58003904,"end":58004648,"strand":1,"description":"long intergenic non-protein coding RNA 1742 [Source:HGNC Symbol;Acc:HGNC:52530]"}, {"versioned_ensembl_gene_id":"ENSG00000279058.2","gene_symbol":"AGAP14","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 14 [Source:HGNC Symbol;Acc:HGNC:23660]","synonyms":"bA145E20.1,AGAP14P,CTGLF11P","biotype":"unprocessed_pseudogene","ncbi_id":"653259","summary":null,"start":46337224,"end":46358714,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 14 [Source:HGNC Symbol;Acc:HGNC:23660]"}, {"versioned_ensembl_gene_id":"ENSG00000226270.3","gene_symbol":"ZNF736P2Y","gene_name":"zinc finger protein 736 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:37727]","synonyms":"ZNF736P2","biotype":"processed_pseudogene","ncbi_id":"392603","summary":null,"start":24683657,"end":24684935,"strand":1,"description":"zinc finger protein 736 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:37727]"}, {"versioned_ensembl_gene_id":"ENSG00000228750.6","gene_symbol":"LINC01672","gene_name":"long intergenic non-protein coding RNA 1672 [Source:HGNC Symbol;Acc:HGNC:52460]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505887","summary":null,"start":6724637,"end":6730012,"strand":1,"description":"long intergenic non-protein coding RNA 1672 [Source:HGNC Symbol;Acc:HGNC:52460]"}, {"versioned_ensembl_gene_id":"ENSG00000244706.2","gene_symbol":"AC026353.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167866500,"end":167870977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253760.1","gene_symbol":"AC009812.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80568050,"end":80568506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257017.8","gene_symbol":"HP","gene_name":"haptoglobin [Source:HGNC Symbol;Acc:HGNC:5141]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3240","summary":"This gene encodes a preproprotein, which is processed to yield both alpha and beta chains, which subsequently combine as a tetramer to produce haptoglobin. Haptoglobin functions to bind free plasma hemoglobin, which allows degradative enzymes to gain access to the hemoglobin, while at the same time preventing loss of iron through the kidneys and protecting the kidneys from damage by hemoglobin. Mutations in this gene and/or its regulatory regions cause ahaptoglobinemia or hypohaptoglobinemia. This gene has also been linked to diabetic nephropathy, the incidence of coronary artery disease in type 1 diabetes, Crohn's disease, inflammatory disease behavior, primary sclerosing cholangitis, susceptibility to idiopathic Parkinson's disease, and a reduced incidence of Plasmodium falciparum malaria. The protein encoded also exhibits antimicrobial activity against bacteria. A similar duplicated gene is located next to this gene on chromosome 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":72054592,"end":72061055,"strand":1,"description":"haptoglobin [Source:HGNC Symbol;Acc:HGNC:5141]"}, {"versioned_ensembl_gene_id":"ENSG00000106034.17","gene_symbol":"CPED1","gene_name":"cadherin like and PC-esterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26159]","synonyms":"FLJ21986,C7orf58","biotype":"protein_coding","ncbi_id":"79974","summary":null,"start":120988677,"end":121297444,"strand":1,"description":"cadherin like and PC-esterase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26159]"}, {"versioned_ensembl_gene_id":"ENSG00000234927.1","gene_symbol":"HMGN1P18","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874444","summary":null,"start":121050927,"end":121051203,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39362]"}, {"versioned_ensembl_gene_id":"ENSG00000157600.11","gene_symbol":"TMEM164","gene_name":"transmembrane protein 164 [Source:HGNC Symbol;Acc:HGNC:26217]","synonyms":"RP13-360B22.2,FLJ22679","biotype":"protein_coding","ncbi_id":"84187","summary":null,"start":110002631,"end":110182734,"strand":1,"description":"transmembrane protein 164 [Source:HGNC Symbol;Acc:HGNC:26217]"}, {"versioned_ensembl_gene_id":"ENSG00000240573.1","gene_symbol":"AC117462.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78087404,"end":78092270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239238.1","gene_symbol":"MEMO1P3","gene_name":"mediator of cell motility 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38503]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462782","summary":null,"start":167888414,"end":167888715,"strand":1,"description":"mediator of cell motility 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38503]"}, {"versioned_ensembl_gene_id":"ENSG00000186980.6","gene_symbol":"KRTAP23-1","gene_name":"keratin associated protein 23-1 [Source:HGNC Symbol;Acc:HGNC:18928]","synonyms":"KAP23.1","biotype":"protein_coding","ncbi_id":"337963","summary":null,"start":30348399,"end":30348609,"strand":-1,"description":"keratin associated protein 23-1 [Source:HGNC Symbol;Acc:HGNC:18928]"}, {"versioned_ensembl_gene_id":"ENSG00000225178.5","gene_symbol":"RPSAP58","gene_name":"ribosomal protein SA pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:36809]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388524","summary":null,"start":23827162,"end":23828049,"strand":1,"description":"ribosomal protein SA pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:36809]"}, {"versioned_ensembl_gene_id":"ENSG00000127481.14","gene_symbol":"UBR4","gene_name":"ubiquitin protein ligase E3 component n-recognin 4 [Source:HGNC Symbol;Acc:HGNC:30313]","synonyms":"ZUBR1,RBAF600,KIAA1307,KIAA0462","biotype":"protein_coding","ncbi_id":"23352","summary":"The protein encoded by this gene is an E3 ubiquitin-protein ligase that interacts with the retinoblastoma-associated protein in the nucleus and with calcium-bound calmodulin in the cytoplasm. The encoded protein appears to be a cytoskeletal component in the cytoplasm and part of the chromatin scaffold in the nucleus. In addition, this protein is a target of the human papillomavirus type 16 E7 oncoprotein. [provided by RefSeq, Aug 2010]","start":19074506,"end":19210276,"strand":-1,"description":"ubiquitin protein ligase E3 component n-recognin 4 [Source:HGNC Symbol;Acc:HGNC:30313]"}, {"versioned_ensembl_gene_id":"ENSG00000251464.2","gene_symbol":"RPL7L1P13","gene_name":"ribosomal protein L7 like 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44212]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133103","summary":null,"start":110399773,"end":110400511,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44212]"}, {"versioned_ensembl_gene_id":"ENSG00000213442.5","gene_symbol":"RPL18AP3","gene_name":"ribosomal protein L18a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31387]","synonyms":"bcm182","biotype":"processed_pseudogene","ncbi_id":"390354","summary":null,"start":104265309,"end":104265836,"strand":1,"description":"ribosomal protein L18a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31387]"}, {"versioned_ensembl_gene_id":"ENSG00000263639.5","gene_symbol":"MSMB","gene_name":"microseminoprotein beta [Source:HGNC Symbol;Acc:HGNC:7372]","synonyms":"IGBF,PSP94,PSP57,PSP-94,PSP,PRPS,PN44,MSPB,MSP","biotype":"protein_coding","ncbi_id":"4477","summary":"The protein encoded by this gene is a member of the immunoglobulin binding factor family. It is synthesized by the epithelial cells of the prostate gland and secreted into the seminal plasma. This protein has inhibin-like activity. It may have a role as an autocrine paracrine factor in uterine, breast and other female reproductive tissues. The expression of the encoded protein is found to be decreased in prostate cancer. Two alternatively spliced transcript variants encoding different isoforms are described for this gene. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]","start":46033307,"end":46046269,"strand":-1,"description":"microseminoprotein beta [Source:HGNC Symbol;Acc:HGNC:7372]"}, {"versioned_ensembl_gene_id":"ENSG00000277336.2","gene_symbol":"CCL3L3","gene_name":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]","synonyms":"MGC12815","biotype":"protein_coding","ncbi_id":"414062","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this gene binds to several chemokine receptors, including chemokine binding protein 2 and chemokine (C-C motif) receptor 5 (CCR5). CCR5 is a co-receptor for HIV, and binding of this protein to CCR5 inhibits HIV entry. The copy number of this gene varies among individuals, where most individuals have one to six copies, and a minority of individuals have zero or more than six copies. There are conflicting reports about copy number variation of this gene and its correlation to disease susceptibility.[provided by RefSeq, Apr 2014]","start":36195241,"end":36197130,"strand":-1,"description":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]"}, {"versioned_ensembl_gene_id":"ENSG00000255150.2","gene_symbol":"EID3","gene_name":"EP300 interacting inhibitor of differentiation 3 [Source:HGNC Symbol;Acc:HGNC:32961]","synonyms":"NSE4B,FLJ25832,NSMCE4B","biotype":"protein_coding","ncbi_id":"493861","summary":null,"start":104303739,"end":104305205,"strand":1,"description":"EP300 interacting inhibitor of differentiation 3 [Source:HGNC Symbol;Acc:HGNC:32961]"}, {"versioned_ensembl_gene_id":"ENSG00000261560.1","gene_symbol":"AC007216.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11881075,"end":11882569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284624.1","gene_symbol":"AC092902.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":125766516,"end":125852936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172137.18","gene_symbol":"CALB2","gene_name":"calbindin 2 [Source:HGNC Symbol;Acc:HGNC:1435]","synonyms":"CAL2","biotype":"protein_coding","ncbi_id":"794","summary":"This gene encodes an intracellular calcium-binding protein belonging to the troponin C superfamily. Members of this protein family have six EF-hand domains which bind calcium. This protein plays a role in diverse cellular functions, including message targeting and intracellular calcium buffering. It also functions as a modulator of neuronal excitability, and is a diagnostic marker for some human diseases, including Hirschsprung disease and some cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":71358713,"end":71390438,"strand":1,"description":"calbindin 2 [Source:HGNC Symbol;Acc:HGNC:1435]"}, {"versioned_ensembl_gene_id":"ENSG00000216523.1","gene_symbol":"AL109941.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84966397,"end":84966625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262434.1","gene_symbol":"AC087392.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":789744,"end":790525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124256.14","gene_symbol":"ZBP1","gene_name":"Z-DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:16176]","synonyms":"DAI,C20orf183,DLM1,DLM-1,dJ718J7.3","biotype":"protein_coding","ncbi_id":"81030","summary":"This gene encodes a Z-DNA binding protein. The encoded protein plays a role in the innate immune response by binding to foreign DNA and inducing type-I interferon production. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":57603846,"end":57620576,"strand":-1,"description":"Z-DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:16176]"}, {"versioned_ensembl_gene_id":"ENSG00000226790.3","gene_symbol":"HNRNPA3P1","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13729]","synonyms":"D10S102,HNRPA3P1,HNRPA3,FBRNP","biotype":"processed_pseudogene","ncbi_id":"10151","summary":"This locus shares sequence similarity with heterogeneous nuclear ribonuclear proteins and represents an apparent transcribed pseudogene of the HNRPA3 gene, which maps to chromosome 2. [provided by RefSeq, Jul 2008]","start":43789249,"end":43790387,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13729]"}, {"versioned_ensembl_gene_id":"ENSG00000223910.1","gene_symbol":"ZNF32-AS3","gene_name":"ZNF32 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:23583]","synonyms":"C10orf44,bA402L1.3","biotype":"antisense_RNA","ncbi_id":"414201","summary":null,"start":43628817,"end":43674703,"strand":1,"description":"ZNF32 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:23583]"}, {"versioned_ensembl_gene_id":"ENSG00000259749.1","gene_symbol":"NCAPGP2","gene_name":"non-SMC condensin I complex subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51905]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421148","summary":null,"start":30005205,"end":30006430,"strand":1,"description":"non-SMC condensin I complex subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51905]"}, {"versioned_ensembl_gene_id":"ENSG00000232553.3","gene_symbol":"CLK2P1","gene_name":"CDC like kinase 2, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2070]","synonyms":"CLK2P","biotype":"processed_pseudogene","ncbi_id":"1197","summary":null,"start":23585062,"end":23586355,"strand":-1,"description":"CDC like kinase 2, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2070]"}, {"versioned_ensembl_gene_id":"ENSG00000274769.1","gene_symbol":"AC016747.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61115787,"end":61164825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228477.1","gene_symbol":"AL663070.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39962680,"end":39963404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237651.6","gene_symbol":"C2orf74","gene_name":"chromosome 2 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:34439]","synonyms":"LOC339804","biotype":"protein_coding","ncbi_id":"339804","summary":null,"start":61145068,"end":61164829,"strand":1,"description":"chromosome 2 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:34439]"}, {"versioned_ensembl_gene_id":"ENSG00000277267.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000104889.5","gene_symbol":"RNASEH2A","gene_name":"ribonuclease H2 subunit A [Source:HGNC Symbol;Acc:HGNC:18518]","synonyms":"AGS4,RNHL,RNHIA,RNASEHI","biotype":"protein_coding","ncbi_id":"10535","summary":"The protein encoded by this gene is a component of the heterotrimeric type II ribonuclease H enzyme (RNAseH2). RNAseH2 is the major source of ribonuclease H activity in mammalian cells and endonucleolytically cleaves ribonucleotides. It is predicted to remove Okazaki fragment RNA primers during lagging strand DNA synthesis and to excise single ribonucleotides from DNA-DNA duplexes. Mutations in this gene cause Aicardi-Goutieres Syndrome (AGS), a an autosomal recessive neurological disorder characterized by progressive microcephaly and psychomotor retardation, intracranial calcifications, elevated levels of interferon-alpha and white blood cells in the cerebrospinal fluid.[provided by RefSeq, Aug 2009]","start":12802063,"end":12813638,"strand":1,"description":"ribonuclease H2 subunit A [Source:HGNC Symbol;Acc:HGNC:18518]"}, {"versioned_ensembl_gene_id":"ENSG00000156709.13","gene_symbol":"AIFM1","gene_name":"apoptosis inducing factor mitochondria associated 1 [Source:HGNC Symbol;Acc:HGNC:8768]","synonyms":"PDCD8,NAMSD,CMTX4,AIF","biotype":"protein_coding","ncbi_id":"9131","summary":"This gene encodes a flavoprotein essential for nuclear disassembly in apoptotic cells, and it is found in the mitochondrial intermembrane space in healthy cells. Induction of apoptosis results in the translocation of this protein to the nucleus where it affects chromosome condensation and fragmentation. In addition, this gene product induces mitochondria to release the apoptogenic proteins cytochrome c and caspase-9. Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6), a severe mitochondrial encephalomyopathy, as well as Cowchock syndrome, also known as X-linked recessive Charcot-Marie-Tooth disease-4 (CMTX-4), a disorder resulting in neuropathy, and axonal and motor-sensory defects with deafness and cognitive disability. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 10. [provided by RefSeq, Aug 2015]","start":130129362,"end":130165887,"strand":-1,"description":"apoptosis inducing factor mitochondria associated 1 [Source:HGNC Symbol;Acc:HGNC:8768]"}, {"versioned_ensembl_gene_id":"ENSG00000133872.13","gene_symbol":"SARAF","gene_name":"store-operated calcium entry associated regulatory factor [Source:HGNC Symbol;Acc:HGNC:28789]","synonyms":"TMEM66,MGC8721","biotype":"protein_coding","ncbi_id":"51669","summary":null,"start":30063012,"end":30083208,"strand":-1,"description":"store-operated calcium entry associated regulatory factor [Source:HGNC Symbol;Acc:HGNC:28789]"}, {"versioned_ensembl_gene_id":"ENSG00000240033.1","gene_symbol":"AC069439.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166835021,"end":166844956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239227.1","gene_symbol":"AC069439.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166861944,"end":166862110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231516.3","gene_symbol":"CBX1P5","gene_name":"chromobox 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:21006]","synonyms":"CBX9","biotype":"processed_pseudogene","ncbi_id":"100133259","summary":null,"start":166811009,"end":166811567,"strand":1,"description":"chromobox 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:21006]"}, {"versioned_ensembl_gene_id":"ENSG00000224659.2","gene_symbol":"GAGE12J","gene_name":"G antigen 12J [Source:HGNC Symbol;Acc:HGNC:17778]","synonyms":"OTTHUMG00000024137,GAGE11","biotype":"protein_coding","ncbi_id":"729396","summary":null,"start":49322057,"end":49329384,"strand":1,"description":"G antigen 12J [Source:HGNC Symbol;Acc:HGNC:17778]"}, {"versioned_ensembl_gene_id":"ENSG00000272502.1","gene_symbol":"AC104958.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120812219,"end":120813359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274343.1","gene_symbol":"AC232323.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85790382,"end":85794399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271381.2","gene_symbol":"REXO1L9P","gene_name":"REXO1 like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44432]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506246","summary":null,"start":85762909,"end":85766931,"strand":-1,"description":"REXO1 like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:44432]"}, {"versioned_ensembl_gene_id":"ENSG00000234535.1","gene_symbol":"AL161719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33610967,"end":33611522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227421.1","gene_symbol":"LINC01724","gene_name":"long intergenic non-protein coding RNA 1724 [Source:HGNC Symbol;Acc:HGNC:52512]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371673","summary":null,"start":196044996,"end":196061073,"strand":-1,"description":"long intergenic non-protein coding RNA 1724 [Source:HGNC Symbol;Acc:HGNC:52512]"}, {"versioned_ensembl_gene_id":"ENSG00000135828.11","gene_symbol":"RNASEL","gene_name":"ribonuclease L [Source:HGNC Symbol;Acc:HGNC:10050]","synonyms":"RNS4,PRCA1","biotype":"protein_coding","ncbi_id":"6041","summary":"This gene encodes a component of the interferon-regulated 2-5A system that functions in the antiviral and antiproliferative roles of interferons. Mutations in this gene have been associated with predisposition to prostate cancer and this gene is a candidate for the hereditary prostate cancer 1 (HPC1) allele. [provided by RefSeq, Jul 2008]","start":182573634,"end":182589256,"strand":-1,"description":"ribonuclease L [Source:HGNC Symbol;Acc:HGNC:10050]"}, {"versioned_ensembl_gene_id":"ENSG00000259677.1","gene_symbol":"AC027176.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89876540,"end":89877285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270619.1","gene_symbol":"AL391358.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118278159,"end":118283367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234524.1","gene_symbol":"RPL12P43","gene_name":"ribosomal protein L12 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35840]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271387","summary":null,"start":118146063,"end":118146561,"strand":1,"description":"ribosomal protein L12 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35840]"}, {"versioned_ensembl_gene_id":"ENSG00000276006.1","gene_symbol":"REXO1L12P","gene_name":"REXO1 like 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:44435]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289448","summary":null,"start":85714922,"end":85715833,"strand":1,"description":"REXO1 like 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:44435]"}, {"versioned_ensembl_gene_id":"ENSG00000149474.13","gene_symbol":"KAT14","gene_name":"lysine acetyltransferase 14 [Source:HGNC Symbol;Acc:HGNC:15904]","synonyms":"PRO1194,dJ717M23.1,CSRP2BP,CRP2BP,ATAC2","biotype":"protein_coding","ncbi_id":"57325","summary":"CSRP2 is a protein containing two LIM domains, which are double zinc finger motifs found in proteins of diverse function. CSRP2 and some related proteins are thought to act as protein adapters, bridging two or more proteins to form a larger protein complex. The protein encoded by this gene binds to one of the LIM domains of CSRP2 and contains an acetyltransferase domain. Although the encoded protein has been detected in the cytoplasm, it is predominantly a nuclear protein. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2011]","start":18138118,"end":18188387,"strand":1,"description":"lysine acetyltransferase 14 [Source:HGNC Symbol;Acc:HGNC:15904]"}, {"versioned_ensembl_gene_id":"ENSG00000146678.9","gene_symbol":"IGFBP1","gene_name":"insulin like growth factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5469]","synonyms":"PP12,IGF-BP25,IBP1,hIGFBP-1,AFBP","biotype":"protein_coding","ncbi_id":"3484","summary":"This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP N-terminal domain and a thyroglobulin type-I domain. The encoded protein, mainly expressed in the liver, circulates in the plasma and binds both insulin-like growth factors (IGFs) I and II, prolonging their half-lives and altering their interaction with cell surface receptors. This protein is important in cell migration and metabolism. Low levels of this protein may be associated with impaired glucose tolerance, vascular disease and hypertension in human patients. [provided by RefSeq, Aug 2017]","start":45888357,"end":45893668,"strand":1,"description":"insulin like growth factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5469]"}, {"versioned_ensembl_gene_id":"ENSG00000228439.5","gene_symbol":"TSTD3","gene_name":"thiosulfate sulfurtransferase (rhodanese)-like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:40910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130890","summary":null,"start":99520693,"end":99531918,"strand":1,"description":"thiosulfate sulfurtransferase (rhodanese)-like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:40910]"}, {"versioned_ensembl_gene_id":"ENSG00000132207.17","gene_symbol":"SLX1A","gene_name":"SLX1 homolog A, structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:20922]","synonyms":"GIYD1","biotype":"protein_coding","ncbi_id":"548593","summary":"This gene encodes a protein that is an important regulator of genome stability. The protein represents the catalytic subunit of the SLX1-SLX4 structure-specific endonuclease, which can resolve DNA secondary structures that are formed during repair and recombination processes. Two identical copies of this gene are located on the p arm of chromosome 16 due to a segmental duplication; this record represents the more centromeric copy. Alternative splicing results in multiple transcript variants. Read-through transcription also occurs between this gene and the downstream SULT1A3 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3) gene. [provided by RefSeq, Nov 2010]","start":30193887,"end":30197561,"strand":1,"description":"SLX1 homolog A, structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:20922]"}, {"versioned_ensembl_gene_id":"ENSG00000262808.2","gene_symbol":"KRTAP1-1","gene_name":"keratin associated protein 1-1 [Source:HGNC Symbol;Acc:HGNC:16772]","synonyms":"KAP1.1B,KAP1.1A,KAP1.1,HB2A","biotype":"protein_coding","ncbi_id":"81851","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41040684,"end":41041586,"strand":-1,"description":"keratin associated protein 1-1 [Source:HGNC Symbol;Acc:HGNC:16772]"}, {"versioned_ensembl_gene_id":"ENSG00000254319.5","gene_symbol":"AC246817.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2666079,"end":2728451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078549.14","gene_symbol":"ADCYAP1R1","gene_name":"ADCYAP receptor type I [Source:HGNC Symbol;Acc:HGNC:242]","synonyms":"PACAPR,PAC1R,PAC1","biotype":"protein_coding","ncbi_id":"117","summary":"This gene encodes type I adenylate cyclase activating polypeptide receptor, which is a membrane-associated protein and shares significant homology with members of the glucagon/secretin receptor family. This receptor mediates diverse biological actions of adenylate cyclase activating polypeptide 1 and is positively coupled to adenylate cyclase. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Dec 2010]","start":31052461,"end":31111479,"strand":1,"description":"ADCYAP receptor type I [Source:HGNC Symbol;Acc:HGNC:242]"}, {"versioned_ensembl_gene_id":"ENSG00000228903.7","gene_symbol":"RASA4CP","gene_name":"RAS p21 protein activator 4C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44185]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401331","summary":null,"start":44026951,"end":44041892,"strand":-1,"description":"RAS p21 protein activator 4C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44185]"}, {"versioned_ensembl_gene_id":"ENSG00000235314.1","gene_symbol":"LINC00957","gene_name":"long intergenic non-protein coding RNA 957 [Source:HGNC Symbol;Acc:HGNC:22332]","synonyms":null,"biotype":"lincRNA","ncbi_id":"255031","summary":null,"start":44039171,"end":44042306,"strand":1,"description":"long intergenic non-protein coding RNA 957 [Source:HGNC Symbol;Acc:HGNC:22332]"}, {"versioned_ensembl_gene_id":"ENSG00000139289.13","gene_symbol":"PHLDA1","gene_name":"pleckstrin homology like domain family A member 1 [Source:HGNC Symbol;Acc:HGNC:8933]","synonyms":"TDAG51,PHRIP,DT1P1B11","biotype":"protein_coding","ncbi_id":"22822","summary":"This gene encodes an evolutionarily conserved proline-histidine rich nuclear protein. The encoded protein may play an important role in the anti-apoptotic effects of insulin-like growth factor-1. [provided by RefSeq, Jul 2008]","start":76025447,"end":76033932,"strand":-1,"description":"pleckstrin homology like domain family A member 1 [Source:HGNC Symbol;Acc:HGNC:8933]"}, {"versioned_ensembl_gene_id":"ENSG00000111245.14","gene_symbol":"MYL2","gene_name":"myosin light chain 2 [Source:HGNC Symbol;Acc:HGNC:7583]","synonyms":"CMH10","biotype":"protein_coding","ncbi_id":"4633","summary":"Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]","start":110910819,"end":110920722,"strand":-1,"description":"myosin light chain 2 [Source:HGNC Symbol;Acc:HGNC:7583]"}, {"versioned_ensembl_gene_id":"ENSG00000169840.4","gene_symbol":"GSX1","gene_name":"GS homeobox 1 [Source:HGNC Symbol;Acc:HGNC:20374]","synonyms":"GSH1,Gsh-1","biotype":"protein_coding","ncbi_id":"219409","summary":null,"start":27792643,"end":27794768,"strand":1,"description":"GS homeobox 1 [Source:HGNC Symbol;Acc:HGNC:20374]"}, {"versioned_ensembl_gene_id":"ENSG00000150275.17","gene_symbol":"PCDH15","gene_name":"protocadherin related 15 [Source:HGNC Symbol;Acc:HGNC:14674]","synonyms":"USH1F,DFNB23,CDHR15","biotype":"protein_coding","ncbi_id":"65217","summary":"This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]","start":53802771,"end":55627942,"strand":-1,"description":"protocadherin related 15 [Source:HGNC Symbol;Acc:HGNC:14674]"}, {"versioned_ensembl_gene_id":"ENSG00000275735.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"cl-49,nkat5,183ActI,CD158J","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738547,"end":54752855,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000227801.8","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"DFNB53,DFNA13,HKE5","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33084308,"end":33114125,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000133124.11","gene_symbol":"IRS4","gene_name":"insulin receptor substrate 4 [Source:HGNC Symbol;Acc:HGNC:6128]","synonyms":"PY160,IRS-4","biotype":"protein_coding","ncbi_id":"8471","summary":"IRS4 encodes the insulin receptor substrate 4, a cytoplasmic protein that contains many potential tyrosine and serine/threonine phosphorylation sites. Tyrosine-phosphorylated IRS4 protein has been shown to associate with cytoplasmic signalling molecules that contain SH2 domains. The IRS4 protein is phosphorylated by the insulin receptor tyrosine kinase upon receptor stimulation.. [provided by RefSeq, Jul 2008]","start":108732482,"end":108736409,"strand":-1,"description":"insulin receptor substrate 4 [Source:HGNC Symbol;Acc:HGNC:6128]"}, {"versioned_ensembl_gene_id":"ENSG00000260548.1","gene_symbol":"AL035425.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":108722070,"end":108732687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237863.2","gene_symbol":"AL035425.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108736011,"end":108738903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146112.11","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30676389,"end":30687895,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000258245.1","gene_symbol":"RPL10P13","gene_name":"ribosomal protein L10 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52346]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390345","summary":null,"start":75688794,"end":75689096,"strand":-1,"description":"ribosomal protein L10 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52346]"}, {"versioned_ensembl_gene_id":"ENSG00000225629.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31132604,"end":31138399,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000163501.6","gene_symbol":"IHH","gene_name":"indian hedgehog [Source:HGNC Symbol;Acc:HGNC:5956]","synonyms":"HHG2,BDA1","biotype":"protein_coding","ncbi_id":"3549","summary":"This gene encodes a member of the hedgehog family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including an N-terminal fragment that is involved in signaling. Hedgehog family proteins are essential secreted signaling molecules that regulate a variety of developmental processes including growth, patterning and morphogenesis. The protein encoded by this gene specifically plays a role in bone growth and differentiation. Mutations in this gene are the cause of brachydactyly type A1, which is characterized by shortening or malformation of the fingers and toes. Mutations in this gene are also the cause of acrocapitofemoral dysplasia. [provided by RefSeq, Nov 2015]","start":219054420,"end":219060467,"strand":-1,"description":"indian hedgehog [Source:HGNC Symbol;Acc:HGNC:5956]"}, {"versioned_ensembl_gene_id":"ENSG00000225191.1","gene_symbol":"AL136455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103926567,"end":103927806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161980.5","gene_symbol":"POLR3K","gene_name":"RNA polymerase III subunit K [Source:HGNC Symbol;Acc:HGNC:14121]","synonyms":"RPC11","biotype":"protein_coding","ncbi_id":"51728","summary":"This gene encodes a small essential subunit of RNA polymerase III, the polymerase responsible for synthesizing transfer and small ribosomal RNAs in eukaryotes. The carboxy-terminal domain of this subunit shares a high degree of sequence similarity to the carboxy-terminal domain of an RNA polymerase II elongation factor. This similarity in sequence is supported by functional studies showing that this subunit is required for proper pausing and termination during transcription. Pseudogenes of this gene are found on chromosomes 13 and 17.[provided by RefSeq, Jul 2010]","start":46407,"end":53628,"strand":-1,"description":"RNA polymerase III subunit K [Source:HGNC Symbol;Acc:HGNC:14121]"}, {"versioned_ensembl_gene_id":"ENSG00000268992.1","gene_symbol":"CDC42EP3P1","gene_name":"CDC42 effector protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49673]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128845","summary":null,"start":23384530,"end":23385293,"strand":1,"description":"CDC42 effector protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49673]"}, {"versioned_ensembl_gene_id":"ENSG00000279969.1","gene_symbol":"AC112172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29200579,"end":29225491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139517.7","gene_symbol":"LNX2","gene_name":"ligand of numb-protein X 2 [Source:HGNC Symbol;Acc:HGNC:20421]","synonyms":"PDZRN1,MGC46315","biotype":"protein_coding","ncbi_id":"222484","summary":null,"start":27545911,"end":27620404,"strand":-1,"description":"ligand of numb-protein X 2 [Source:HGNC Symbol;Acc:HGNC:20421]"}, {"versioned_ensembl_gene_id":"ENSG00000282933.2","gene_symbol":"RHOXF1P3","gene_name":"Rhox homeobox family member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51612]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107075307","summary":null,"start":119942834,"end":119992810,"strand":1,"description":"Rhox homeobox family member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51612]"}, {"versioned_ensembl_gene_id":"ENSG00000142687.17","gene_symbol":"KIAA0319L","gene_name":"KIAA0319 like [Source:HGNC Symbol;Acc:HGNC:30071]","synonyms":"KIAA1837","biotype":"protein_coding","ncbi_id":"79932","summary":"This gene is a candidate gene for dyslexia susceptibility.[provided by RefSeq, Apr 2009]","start":35433490,"end":35557950,"strand":-1,"description":"KIAA0319 like [Source:HGNC Symbol;Acc:HGNC:30071]"}, {"versioned_ensembl_gene_id":"ENSG00000254665.1","gene_symbol":"AC091053.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8693357,"end":8696607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267934.1","gene_symbol":"AC010300.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23323968,"end":23329101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275201.1","gene_symbol":"AC074140.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23479762,"end":23480468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203963.11","gene_symbol":"C1orf141","gene_name":"chromosome 1 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:32044]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400757","summary":null,"start":67092165,"end":67231853,"strand":-1,"description":"chromosome 1 open reading frame 141 [Source:HGNC Symbol;Acc:HGNC:32044]"}, {"versioned_ensembl_gene_id":"ENSG00000240231.1","gene_symbol":"RPS27P29","gene_name":"ribosomal protein S27 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36516]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132291","summary":null,"start":23597341,"end":23597592,"strand":1,"description":"ribosomal protein S27 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36516]"}, {"versioned_ensembl_gene_id":"ENSG00000110448.10","gene_symbol":"CD5","gene_name":"CD5 molecule [Source:HGNC Symbol;Acc:HGNC:1685]","synonyms":"T1,LEU1","biotype":"protein_coding","ncbi_id":"921","summary":"This gene encodes a member of the scavenger receptor cysteine-rich (SRCR) superfamily. Members of this family are secreted or membrane-anchored proteins mainly found in cells associated with the immune system. This protein is a type-I transmembrane glycoprotein found on the surface of thymocytes, T lymphocytes and a subset of B lymphocytes. The encoded protein contains three SRCR domains and may act as a receptor to regulate T-cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2016]","start":61102395,"end":61127852,"strand":1,"description":"CD5 molecule [Source:HGNC Symbol;Acc:HGNC:1685]"}, {"versioned_ensembl_gene_id":"ENSG00000268908.1","gene_symbol":"VN1R92P","gene_name":"vomeronasal 1 receptor 92 pseudogene [Source:HGNC Symbol;Acc:HGNC:37412]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312837","summary":null,"start":23444262,"end":23445189,"strand":1,"description":"vomeronasal 1 receptor 92 pseudogene [Source:HGNC Symbol;Acc:HGNC:37412]"}, {"versioned_ensembl_gene_id":"ENSG00000248505.1","gene_symbol":"LINC02380","gene_name":"long intergenic non-protein coding RNA 2380 [Source:HGNC Symbol;Acc:HGNC:53303]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928851","summary":null,"start":57425872,"end":57465986,"strand":1,"description":"long intergenic non-protein coding RNA 2380 [Source:HGNC Symbol;Acc:HGNC:53303]"}, {"versioned_ensembl_gene_id":"ENSG00000213048.3","gene_symbol":"OR5S1P","gene_name":"olfactory receptor family 5 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15040]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"391496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":240109102,"end":240110052,"strand":1,"description":"olfactory receptor family 5 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15040]"}, {"versioned_ensembl_gene_id":"ENSG00000117385.15","gene_symbol":"P3H1","gene_name":"prolyl 3-hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:19316]","synonyms":"GROS1,MGC117314,LEPRECAN,LEPRE1","biotype":"protein_coding","ncbi_id":"64175","summary":"This gene encodes an enzyme that is a member of the collagen prolyl hydroxylase family. These enzymes are localized to the endoplasmic reticulum and their activity is required for proper collagen synthesis and assembly. Mutations in this gene are associated with osteogenesis imperfecta type VIII. Three alternatively spliced transcript variants encoding different isoforms have been described. Other variants may exist, but their biological validity has not been determined. [provided by RefSeq, Aug 2011]","start":42746335,"end":42767084,"strand":-1,"description":"prolyl 3-hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:19316]"}, {"versioned_ensembl_gene_id":"ENSG00000211657.3","gene_symbol":"IGLV3-32","gene_name":"immunoglobulin lambda variable 3-32 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5914]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28787","summary":null,"start":22594528,"end":22595056,"strand":1,"description":"immunoglobulin lambda variable 3-32 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5914]"}, {"versioned_ensembl_gene_id":"ENSG00000211656.3","gene_symbol":"IGLV2-33","gene_name":"immunoglobulin lambda variable 2-33 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5892]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28811","summary":null,"start":22588155,"end":22588688,"strand":1,"description":"immunoglobulin lambda variable 2-33 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5892]"}, {"versioned_ensembl_gene_id":"ENSG00000228037.1","gene_symbol":"AL139246.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2581560,"end":2584533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225931.3","gene_symbol":"AL139246.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2566410,"end":2569888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148429.14","gene_symbol":"USP6NL","gene_name":"USP6 N-terminal like [Source:HGNC Symbol;Acc:HGNC:16858]","synonyms":"KIAA0019,USP6NL-IT1,TRE2NL,RNTRE,RN-tre","biotype":"protein_coding","ncbi_id":"9712","summary":null,"start":11453946,"end":11611754,"strand":-1,"description":"USP6 N-terminal like [Source:HGNC Symbol;Acc:HGNC:16858]"}, {"versioned_ensembl_gene_id":"ENSG00000232634.1","gene_symbol":"NEFLP1","gene_name":"neurofilament light pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37662]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359795","summary":null,"start":21221106,"end":21222089,"strand":-1,"description":"neurofilament light pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37662]"}, {"versioned_ensembl_gene_id":"ENSG00000204843.12","gene_symbol":"DCTN1","gene_name":"dynactin subunit 1 [Source:HGNC Symbol;Acc:HGNC:2711]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1639","summary":"This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains directly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA). [provided by RefSeq, Oct 2008]","start":74361154,"end":74392087,"strand":-1,"description":"dynactin subunit 1 [Source:HGNC Symbol;Acc:HGNC:2711]"}, {"versioned_ensembl_gene_id":"ENSG00000276459.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738512,"end":54753028,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000271895.2","gene_symbol":"AL109811.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11029659,"end":11030528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233155.1","gene_symbol":"HMGA1P8","gene_name":"high mobility group AT-hook 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39183]","synonyms":"HMGA1-p","biotype":"processed_pseudogene","ncbi_id":"100130009","summary":null,"start":74418122,"end":74418442,"strand":-1,"description":"high mobility group AT-hook 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39183]"}, {"versioned_ensembl_gene_id":"ENSG00000269139.2","gene_symbol":"AC010336.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7926001,"end":7926810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284233.1","gene_symbol":"AP000356.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24633272,"end":24633443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124786.9","gene_symbol":"SLC35B3","gene_name":"solute carrier family 35 member B3 [Source:HGNC Symbol;Acc:HGNC:21601]","synonyms":"dJ453H5.1,CGI-19,C6orf196,PAPST2","biotype":"protein_coding","ncbi_id":"51000","summary":"This gene is a member of the solute carrier family. The encoded protein is involved in the transport of 3-prime phosphoadenosine 5-prime phosphosulfate (PAPS) from the nucleus or the cytosol to the Golgi lumen. This gene has been reported to be expressed preferentially in the human colon tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":8413068,"end":8435483,"strand":-1,"description":"solute carrier family 35 member B3 [Source:HGNC Symbol;Acc:HGNC:21601]"}, {"versioned_ensembl_gene_id":"ENSG00000047936.10","gene_symbol":"ROS1","gene_name":"ROS proto-oncogene 1, receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:10261]","synonyms":"c-ros-1,ROS,MCF3","biotype":"protein_coding","ncbi_id":"6098","summary":"This proto-oncogene, highly-expressed in a variety of tumor cell lines, belongs to the sevenless subfamily of tyrosine kinase insulin receptor genes. The protein encoded by this gene is a type I integral membrane protein with tyrosine kinase activity. The protein may function as a growth or differentiation factor receptor. [provided by RefSeq, Jul 2008]","start":117288300,"end":117425855,"strand":-1,"description":"ROS proto-oncogene 1, receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:10261]"}, {"versioned_ensembl_gene_id":"ENSG00000267456.2","gene_symbol":"AC023043.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36278735,"end":36279119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149503.12","gene_symbol":"INCENP","gene_name":"inner centromere protein [Source:HGNC Symbol;Acc:HGNC:6058]","synonyms":"FLJ31633","biotype":"protein_coding","ncbi_id":"3619","summary":"In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger,' or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (centromere protein A; MIM 117139), CENPB (MIM 117140), CENPC1 (MIM 117141), and CENPD (MIM 117142). The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle (Earnshaw and Mackay, 1994 [PubMed 8088460]). These include CENPE (MIM 117143); MCAK (MIM 604538); KID (MIM 603213); cytoplasmic dynein (e.g., MIM 600112); CliPs (e.g., MIM 179838); and CENPF/mitosin (MIM 600236). The inner centromere proteins (INCENPs) (Earnshaw and Cooke, 1991 [PubMed 1860899]), the initial members of the passenger protein group, display a broad localization along chromosomes in the early stages of mitosis but gradually become concentrated at centromeres as the cell cycle progresses into mid-metaphase. During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis (Cutts et al., 1999 [PubMed 10369859]).[supplied by OMIM, Mar 2008]","start":62123973,"end":62153163,"strand":1,"description":"inner centromere protein [Source:HGNC Symbol;Acc:HGNC:6058]"}, {"versioned_ensembl_gene_id":"ENSG00000258721.2","gene_symbol":"OR11H3P","gene_name":"olfactory receptor family 11 subfamily H member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15367]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81113","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22009548,"end":22010529,"strand":-1,"description":"olfactory receptor family 11 subfamily H member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15367]"}, {"versioned_ensembl_gene_id":"ENSG00000259324.1","gene_symbol":"OR11K1P","gene_name":"olfactory receptor family 11 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15371]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81109","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22030931,"end":22031834,"strand":-1,"description":"olfactory receptor family 11 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15371]"}, {"versioned_ensembl_gene_id":"ENSG00000274102.1","gene_symbol":"OR4M2","gene_name":"olfactory receptor family 4 subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:15373]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390538","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22080527,"end":22081659,"strand":1,"description":"olfactory receptor family 4 subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:15373]"}, {"versioned_ensembl_gene_id":"ENSG00000279296.1","gene_symbol":"PRAL","gene_name":"p53 regulation associated lncRNA [Source:HGNC Symbol;Acc:HGNC:52646]","synonyms":"lncRNA-PRAL","biotype":"TEC","ncbi_id":"109245082","summary":null,"start":6772831,"end":6776116,"strand":-1,"description":"p53 regulation associated lncRNA [Source:HGNC Symbol;Acc:HGNC:52646]"}, {"versioned_ensembl_gene_id":"ENSG00000132530.16","gene_symbol":"XAF1","gene_name":"XIAP associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30932]","synonyms":"XIAPAF1,HSXIAPAF1,BIRC4BP","biotype":"protein_coding","ncbi_id":"54739","summary":"This gene encodes a protein which binds to and counteracts the inhibitory effect of a member of the IAP (inhibitor of apoptosis) protein family. IAP proteins bind to and inhibit caspases which are activated during apoptosis. The proportion of IAPs and proteins which interfere with their activity, such as the encoded protein, affect the progress of the apoptosis signaling pathway. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":6755447,"end":6775647,"strand":1,"description":"XIAP associated factor 1 [Source:HGNC Symbol;Acc:HGNC:30932]"}, {"versioned_ensembl_gene_id":"ENSG00000240204.2","gene_symbol":"SMKR1","gene_name":"small lysine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:43561]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287482","summary":null,"start":129502479,"end":129512932,"strand":1,"description":"small lysine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:43561]"}, {"versioned_ensembl_gene_id":"ENSG00000234763.1","gene_symbol":"AL359378.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8341937,"end":8343021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123572.16","gene_symbol":"NRK","gene_name":"Nik related kinase [Source:HGNC Symbol;Acc:HGNC:25391]","synonyms":"DKFZp686A17109","biotype":"protein_coding","ncbi_id":"203447","summary":"The mouse ortholog of this gene encodes a protein kinase required for JNK activation. The encoded protein may be involved in the induction of actin polymerization in late embryogenesis.[provided by RefSeq, Jun 2010]","start":105822543,"end":105958610,"strand":1,"description":"Nik related kinase [Source:HGNC Symbol;Acc:HGNC:25391]"}, {"versioned_ensembl_gene_id":"ENSG00000178531.5","gene_symbol":"CTXN1","gene_name":"cortexin 1 [Source:HGNC Symbol;Acc:HGNC:31108]","synonyms":"FLJ25968","biotype":"protein_coding","ncbi_id":"404217","summary":null,"start":7924485,"end":7926166,"strand":-1,"description":"cortexin 1 [Source:HGNC Symbol;Acc:HGNC:31108]"}, {"versioned_ensembl_gene_id":"ENSG00000219703.1","gene_symbol":"RAP1BP3","gene_name":"RAP1B, member of RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132917","summary":null,"start":117431591,"end":117432442,"strand":1,"description":"RAP1B, member of RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49782]"}, {"versioned_ensembl_gene_id":"ENSG00000229332.2","gene_symbol":"PGBD4P8","gene_name":"piggyBac transposable element derived 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44075]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421185","summary":null,"start":60097415,"end":60097976,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44075]"}, {"versioned_ensembl_gene_id":"ENSG00000184752.12","gene_symbol":"NDUFA12","gene_name":"NADH:ubiquinone oxidoreductase subunit A12 [Source:HGNC Symbol;Acc:HGNC:23987]","synonyms":"DAP13,B17.2","biotype":"protein_coding","ncbi_id":"55967","summary":"This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]","start":94897055,"end":95003770,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A12 [Source:HGNC Symbol;Acc:HGNC:23987]"}, {"versioned_ensembl_gene_id":"ENSG00000137080.4","gene_symbol":"IFNA21","gene_name":"interferon alpha 21 [Source:HGNC Symbol;Acc:HGNC:5424]","synonyms":"IFN-alphaI","biotype":"protein_coding","ncbi_id":"3452","summary":"This gene is a member of the alpha interferon gene cluster on the short arm of chromosome 9. Interferons are cytokines produced in response to viral infection that mediate the immune response and interfere with viral replication. The encoded protein is a type I interferon and may play a specific role in the antiviral response to rubella virus. [provided by RefSeq, Sep 2011]","start":21165637,"end":21166660,"strand":-1,"description":"interferon alpha 21 [Source:HGNC Symbol;Acc:HGNC:5424]"}, {"versioned_ensembl_gene_id":"ENSG00000259607.1","gene_symbol":"AC108449.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29067279,"end":29068454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004948.13","gene_symbol":"CALCR","gene_name":"calcitonin receptor [Source:HGNC Symbol;Acc:HGNC:1440]","synonyms":"CTR","biotype":"protein_coding","ncbi_id":"799","summary":"This gene encodes a high affinity receptor for the peptide hormone calcitonin and belongs to a subfamily of seven transmembrane-spanning G protein-coupled receptors. The encoded protein is involved in maintaining calcium homeostasis and in regulating osteoclast-mediated bone resorption. Polymorphisms in this gene have been associated with variations in bone mineral density and onset of osteoporosis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":93424487,"end":93574730,"strand":-1,"description":"calcitonin receptor [Source:HGNC Symbol;Acc:HGNC:1440]"}, {"versioned_ensembl_gene_id":"ENSG00000227081.5","gene_symbol":"AC005912.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3211663,"end":3211917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180900.18","gene_symbol":"SCRIB","gene_name":"scribbled planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:30377]","synonyms":"Vartul,SCRB1,KIAA0147","biotype":"protein_coding","ncbi_id":"23513","summary":"This gene encodes a protein that was identified as being similar to the Drosophila scribble protein. The mammalian protein is involved in tumor suppression pathways. As a scaffold protein involved in cell polarization processes, this protein binds to many other proteins. The encoded protein binds to papillomavirus E6 protein via its PDZ domain and the C-terminus of E6. Two alternatively spliced transcript variants that encode different protein isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":143790920,"end":143815379,"strand":-1,"description":"scribbled planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:30377]"}, {"versioned_ensembl_gene_id":"ENSG00000229842.2","gene_symbol":"MTATP6P13","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52058]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075272","summary":null,"start":93925406,"end":93926072,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52058]"}, {"versioned_ensembl_gene_id":"ENSG00000251504.1","gene_symbol":"LINC01099","gene_name":"long intergenic non-protein coding RNA 1099 [Source:HGNC Symbol;Acc:HGNC:49222]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928656","summary":null,"start":177729638,"end":177907936,"strand":-1,"description":"long intergenic non-protein coding RNA 1099 [Source:HGNC Symbol;Acc:HGNC:49222]"}, {"versioned_ensembl_gene_id":"ENSG00000280206.1","gene_symbol":"AC026401.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15701237,"end":15702118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243336.5","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"D6S203,HLA-CDA12,CDA12,HLA-59","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":29996088,"end":29999447,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000235338.1","gene_symbol":"DUSP5P2","gene_name":"dual specificity phosphatase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44482]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643459","summary":null,"start":9600748,"end":9602728,"strand":1,"description":"dual specificity phosphatase 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44482]"}, {"versioned_ensembl_gene_id":"ENSG00000126545.13","gene_symbol":"CSN1S1","gene_name":"casein alpha s1 [Source:HGNC Symbol;Acc:HGNC:2445]","synonyms":"CASA,CSN1","biotype":"protein_coding","ncbi_id":"1446","summary":null,"start":69931081,"end":69946574,"strand":1,"description":"casein alpha s1 [Source:HGNC Symbol;Acc:HGNC:2445]"}, {"versioned_ensembl_gene_id":"ENSG00000205884.2","gene_symbol":"DEFB136","gene_name":"defensin beta 136 [Source:HGNC Symbol;Acc:HGNC:34433]","synonyms":"DEFB137","biotype":"protein_coding","ncbi_id":"613210","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 8p23. [provided by RefSeq, Nov 2014]","start":11973937,"end":11974599,"strand":-1,"description":"defensin beta 136 [Source:HGNC Symbol;Acc:HGNC:34433]"}, {"versioned_ensembl_gene_id":"ENSG00000214842.5","gene_symbol":"RAD51AP2","gene_name":"RAD51 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:34417]","synonyms":"FLJ17540","biotype":"protein_coding","ncbi_id":"729475","summary":null,"start":17510584,"end":17518439,"strand":-1,"description":"RAD51 associated protein 2 [Source:HGNC Symbol;Acc:HGNC:34417]"}, {"versioned_ensembl_gene_id":"ENSG00000162598.13","gene_symbol":"C1orf87","gene_name":"chromosome 1 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:28547]","synonyms":"MGC34837,CREF","biotype":"protein_coding","ncbi_id":"127795","summary":null,"start":59987269,"end":60073770,"strand":-1,"description":"chromosome 1 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:28547]"}, {"versioned_ensembl_gene_id":"ENSG00000237490.3","gene_symbol":"RPS27AP17","gene_name":"ribosomal protein S27a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36877]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392425","summary":null,"start":6989329,"end":6989783,"strand":1,"description":"ribosomal protein S27a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36877]"}, {"versioned_ensembl_gene_id":"ENSG00000174171.5","gene_symbol":"AC020659.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41892793,"end":41898575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267663.1","gene_symbol":"AP005264.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12246589,"end":12247055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269898.1","gene_symbol":"AC018695.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85743287,"end":85744225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213358.3","gene_symbol":"AC092933.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":196527339,"end":196528791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154102.10","gene_symbol":"C16orf74","gene_name":"chromosome 16 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:23362]","synonyms":"MGC17624","biotype":"protein_coding","ncbi_id":"404550","summary":null,"start":85690084,"end":85751129,"strand":-1,"description":"chromosome 16 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:23362]"}, {"versioned_ensembl_gene_id":"ENSG00000278767.4","gene_symbol":"SERPINA10","gene_name":"serpin family A member 10 [Source:HGNC Symbol;Acc:HGNC:15996]","synonyms":"ZPI,PZI","biotype":"protein_coding","ncbi_id":"51156","summary":"The protein encoded by this gene belongs to the serpin family. It is predominantly expressed in the liver and secreted in plasma. It inhibits the activity of coagulation factors Xa and XIa in the presence of protein Z, calcium and phospholipid. Mutations in this gene are associated with venous thrombosis. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, May 2010]","start":94280460,"end":94293271,"strand":-1,"description":"serpin family A member 10 [Source:HGNC Symbol;Acc:HGNC:15996]"}, {"versioned_ensembl_gene_id":"ENSG00000275865.2","gene_symbol":"SPACA7","gene_name":"sperm acrosome associated 7 [Source:HGNC Symbol;Acc:HGNC:29575]","synonyms":"C13orf28","biotype":"protein_coding","ncbi_id":"122258","summary":null,"start":112360163,"end":112418533,"strand":1,"description":"sperm acrosome associated 7 [Source:HGNC Symbol;Acc:HGNC:29575]"}, {"versioned_ensembl_gene_id":"ENSG00000234211.2","gene_symbol":"AL451067.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161671978,"end":161674824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263590.2","gene_symbol":"AC239800.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143790010,"end":143797108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148396.18","gene_symbol":"SEC16A","gene_name":"SEC16 homolog A, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:29006]","synonyms":"Sec16L,p250,KIAA0310","biotype":"protein_coding","ncbi_id":"9919","summary":"This gene encodes a protein that forms part of the Sec16 complex. This protein has a role in protein transport from the endoplasmic reticulum (ER) to the Golgi and mediates COPII vesicle formation at the transitional ER. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Feb 2013]","start":136440096,"end":136483759,"strand":-1,"description":"SEC16 homolog A, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:29006]"}, {"versioned_ensembl_gene_id":"ENSG00000140092.14","gene_symbol":"FBLN5","gene_name":"fibulin 5 [Source:HGNC Symbol;Acc:HGNC:3602]","synonyms":"ARMD3,UP50,EVEC,DANCE","biotype":"protein_coding","ncbi_id":"10516","summary":"The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq, Jul 2008]","start":91869412,"end":91947987,"strand":-1,"description":"fibulin 5 [Source:HGNC Symbol;Acc:HGNC:3602]"}, {"versioned_ensembl_gene_id":"ENSG00000172724.11","gene_symbol":"CCL19","gene_name":"C-C motif chemokine ligand 19 [Source:HGNC Symbol;Acc:HGNC:10617]","synonyms":"CKb11,SCYA19,MIP-3b,exodus-3,ELC","biotype":"protein_coding","ncbi_id":"6363","summary":"This antimicrobial gene is one of several CC cytokine genes clustered on the p-arm of chromosome 9. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene may play a role in normal lymphocyte recirculation and homing. It also plays an important role in trafficking of T cells in thymus, and in T cell and B cell migration to secondary lymphoid organs. It specifically binds to chemokine receptor CCR7. [provided by RefSeq, Sep 2014]","start":34689567,"end":34691277,"strand":-1,"description":"C-C motif chemokine ligand 19 [Source:HGNC Symbol;Acc:HGNC:10617]"}, {"versioned_ensembl_gene_id":"ENSG00000280208.1","gene_symbol":"GGT4P","gene_name":"gamma-glutamyltransferase 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33207]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643171","summary":null,"start":18253526,"end":18270822,"strand":-1,"description":"gamma-glutamyltransferase 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33207]"}, {"versioned_ensembl_gene_id":"ENSG00000091009.7","gene_symbol":"RBM27","gene_name":"RNA binding motif protein 27 [Source:HGNC Symbol;Acc:HGNC:29243]","synonyms":"ZC3H20,Psc1,KIAA1311,ARRS1","biotype":"protein_coding","ncbi_id":"54439","summary":null,"start":146203600,"end":146289132,"strand":1,"description":"RNA binding motif protein 27 [Source:HGNC Symbol;Acc:HGNC:29243]"}, {"versioned_ensembl_gene_id":"ENSG00000180878.2","gene_symbol":"C11orf42","gene_name":"chromosome 11 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:28541]","synonyms":"MGC34805","biotype":"protein_coding","ncbi_id":"160298","summary":null,"start":6205566,"end":6211132,"strand":1,"description":"chromosome 11 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:28541]"}, {"versioned_ensembl_gene_id":"ENSG00000249192.1","gene_symbol":"MTND3P25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52172]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075297","summary":null,"start":134928393,"end":134928527,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52172]"}, {"versioned_ensembl_gene_id":"ENSG00000244246.1","gene_symbol":"ZNF736P8Y","gene_name":"zinc finger protein 736 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:38406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419724","summary":null,"start":7913422,"end":7914090,"strand":-1,"description":"zinc finger protein 736 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:38406]"}, {"versioned_ensembl_gene_id":"ENSG00000215102.2","gene_symbol":"TERF1P4","gene_name":"telomeric repeat binding factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648283","summary":null,"start":83748825,"end":83749939,"strand":-1,"description":"telomeric repeat binding factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38500]"}, {"versioned_ensembl_gene_id":"ENSG00000254601.1","gene_symbol":"CYCSP26","gene_name":"cytochrome c, somatic pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:24400]","synonyms":"HCP26","biotype":"processed_pseudogene","ncbi_id":"360178","summary":null,"start":58005386,"end":58005705,"strand":1,"description":"cytochrome c, somatic pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:24400]"}, {"versioned_ensembl_gene_id":"ENSG00000219384.1","gene_symbol":"AL138880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45158870,"end":45159511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236807.1","gene_symbol":"AC092066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44765148,"end":44765464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129347.19","gene_symbol":"KRI1","gene_name":"KRI1 homolog [Source:HGNC Symbol;Acc:HGNC:25769]","synonyms":"FLJ12949","biotype":"protein_coding","ncbi_id":"65095","summary":"This gene overlaps with the gene for cysteine endopeptidase AUT-like 4 in a head-to-tail orientation. [provided by RefSeq, Jul 2008]","start":10553078,"end":10566037,"strand":-1,"description":"KRI1 homolog [Source:HGNC Symbol;Acc:HGNC:25769]"}, {"versioned_ensembl_gene_id":"ENSG00000275441.1","gene_symbol":"AC020765.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28553709,"end":28554140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235339.1","gene_symbol":"GEMIN2P2","gene_name":"gem nuclear organelle associated protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287063","summary":null,"start":41977008,"end":41978034,"strand":1,"description":"gem nuclear organelle associated protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49562]"}, {"versioned_ensembl_gene_id":"ENSG00000227946.1","gene_symbol":"AC007383.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206084605,"end":206086564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163219.11","gene_symbol":"ARHGAP25","gene_name":"Rho GTPase activating protein 25 [Source:HGNC Symbol;Acc:HGNC:28951]","synonyms":"KIAA0053","biotype":"protein_coding","ncbi_id":"9938","summary":"ARHGAPs, such as ARHGAP25, encode negative regulators of Rho GTPases (see ARHA; MIM 165390), which are implicated in actin remodeling, cell polarity, and cell migration (Katoh and Katoh, 2004 [PubMed 15254788]).[supplied by OMIM, Mar 2008]","start":68679601,"end":68826833,"strand":1,"description":"Rho GTPase activating protein 25 [Source:HGNC Symbol;Acc:HGNC:28951]"}, {"versioned_ensembl_gene_id":"ENSG00000234895.1","gene_symbol":"OR52X1P","gene_name":"olfactory receptor family 52 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14790]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"79272","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6066873,"end":6067786,"strand":-1,"description":"olfactory receptor family 52 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14790]"}, {"versioned_ensembl_gene_id":"ENSG00000185837.3","gene_symbol":"HDHD5-AS1","gene_name":"HDHD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1842]","synonyms":"NCRNA00017,CECR5-AS1,CECR4","biotype":"antisense_RNA","ncbi_id":"100130717","summary":null,"start":17159384,"end":17165445,"strand":1,"description":"HDHD5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1842]"}, {"versioned_ensembl_gene_id":"ENSG00000113761.11","gene_symbol":"ZNF346","gene_name":"zinc finger protein 346 [Source:HGNC Symbol;Acc:HGNC:16403]","synonyms":"Zfp346,JAZ","biotype":"protein_coding","ncbi_id":"23567","summary":"The protein encoded by this gene is a nucleolar, zinc finger protein that preferentially binds to double-stranded (ds) RNA or RNA/DNA hybrids, rather than DNA alone. Mutational studies indicate that the zinc finger domains are not only essential for dsRNA binding, but are also required for its nucleolar localization. The encoded protein may be involved in cell growth and survival. It plays a role in protecting neurons by inhibiting cell cycle re-entry via stimulation of p21 gene expression. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":177022696,"end":177081189,"strand":1,"description":"zinc finger protein 346 [Source:HGNC Symbol;Acc:HGNC:16403]"}, {"versioned_ensembl_gene_id":"ENSG00000269940.1","gene_symbol":"AL049840.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":103694560,"end":103695170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223819.2","gene_symbol":"Z95327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100800303,"end":100800784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127311.9","gene_symbol":"HELB","gene_name":"DNA helicase B [Source:HGNC Symbol;Acc:HGNC:17196]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92797","summary":"This gene encodes a DNA-dependent ATPase which catalyzes the unwinding of DNA necessary for DNA replication, repair, recombination, and transcription. This gene is thought to function specifically during the S phase entry of the cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":66302545,"end":66347645,"strand":1,"description":"DNA helicase B [Source:HGNC Symbol;Acc:HGNC:17196]"}, {"versioned_ensembl_gene_id":"ENSG00000137691.12","gene_symbol":"C11orf70","gene_name":"chromosome 11 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:28188]","synonyms":"MGC13040","biotype":"protein_coding","ncbi_id":"85016","summary":null,"start":102047443,"end":102084560,"strand":1,"description":"chromosome 11 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:28188]"}, {"versioned_ensembl_gene_id":"ENSG00000188459.4","gene_symbol":"WASF4P","gene_name":"WAS protein family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:20801]","synonyms":"WASF4","biotype":"processed_pseudogene","ncbi_id":"644739","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, most closely resembles the gene encoding the WAS protein family member 2, which is located on chromosome 1. [provided by RefSeq, Jul 2008]","start":47803296,"end":47804789,"strand":1,"description":"WAS protein family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:20801]"}, {"versioned_ensembl_gene_id":"ENSG00000236423.5","gene_symbol":"LINC01134","gene_name":"long intergenic non-protein coding RNA 1134 [Source:HGNC Symbol;Acc:HGNC:49449]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133612","summary":null,"start":3900372,"end":3917225,"strand":1,"description":"long intergenic non-protein coding RNA 1134 [Source:HGNC Symbol;Acc:HGNC:49449]"}, {"versioned_ensembl_gene_id":"ENSG00000154328.15","gene_symbol":"NEIL2","gene_name":"nei like DNA glycosylase 2 [Source:HGNC Symbol;Acc:HGNC:18956]","synonyms":"FLJ31644,NEH2,MGC4505,MGC2832","biotype":"protein_coding","ncbi_id":"252969","summary":"This gene encodes a member of the Fpg/Nei family of DNA glycosylases. These glycosylases initiate the first step in base excision repair by cleaving oxidatively damaged bases and introducing a DNA strand break via their abasic site lyase activity. This enzyme is primarily associated with DNA repair during transcription and acts prefentially on cytosine-derived lesions, particularly 5-hydroxyuracil and 5-hydroxycytosine. It contains an N-terminal catalytic domain, a hinge region, and a C-terminal DNA-binding domain with helix-two-turn-helix and zinc finger motifs. This enzyme interacts with the X-ray cross complementing factor 1 scaffold protein as part of a multi-protein DNA repair complex. A pseudogene of this gene has been identified. [provided by RefSeq, Mar 2017]","start":11769639,"end":11787346,"strand":1,"description":"nei like DNA glycosylase 2 [Source:HGNC Symbol;Acc:HGNC:18956]"}, {"versioned_ensembl_gene_id":"ENSG00000146828.17","gene_symbol":"SLC12A9","gene_name":"solute carrier family 12 member 9 [Source:HGNC Symbol;Acc:HGNC:17435]","synonyms":"CIP1","biotype":"protein_coding","ncbi_id":"56996","summary":null,"start":100826820,"end":100867009,"strand":1,"description":"solute carrier family 12 member 9 [Source:HGNC Symbol;Acc:HGNC:17435]"}, {"versioned_ensembl_gene_id":"ENSG00000227587.2","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"NG38,ATP6G,Em:AC004181.3,Vma10,ATP6G2","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31531911,"end":31534293,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000229758.2","gene_symbol":"DYNLT3P2","gene_name":"dynein light chain Tctex-type 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100381215","summary":null,"start":128199901,"end":128200195,"strand":1,"description":"dynein light chain Tctex-type 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37081]"}, {"versioned_ensembl_gene_id":"ENSG00000233729.1","gene_symbol":"AC016909.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132915557,"end":132931494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100075.9","gene_symbol":"SLC25A1","gene_name":"solute carrier family 25 member 1 [Source:HGNC Symbol;Acc:HGNC:10979]","synonyms":"SLC20A3,CTP","biotype":"protein_coding","ncbi_id":"6576","summary":"This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":19175575,"end":19178830,"strand":-1,"description":"solute carrier family 25 member 1 [Source:HGNC Symbol;Acc:HGNC:10979]"}, {"versioned_ensembl_gene_id":"ENSG00000124491.15","gene_symbol":"F13A1","gene_name":"coagulation factor XIII A chain [Source:HGNC Symbol;Acc:HGNC:3531]","synonyms":"F13A","biotype":"protein_coding","ncbi_id":"2162","summary":"This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]","start":6144085,"end":6321013,"strand":-1,"description":"coagulation factor XIII A chain [Source:HGNC Symbol;Acc:HGNC:3531]"}, {"versioned_ensembl_gene_id":"ENSG00000227336.1","gene_symbol":"LINC00434","gene_name":"long intergenic non-protein coding RNA 434 [Source:HGNC Symbol;Acc:HGNC:42769]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874169","summary":null,"start":60214352,"end":60214946,"strand":-1,"description":"long intergenic non-protein coding RNA 434 [Source:HGNC Symbol;Acc:HGNC:42769]"}, {"versioned_ensembl_gene_id":"ENSG00000196236.12","gene_symbol":"XPNPEP3","gene_name":"X-prolyl aminopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:28052]","synonyms":"NPHPL1,ICP55,APP3","biotype":"protein_coding","ncbi_id":"63929","summary":"The protein encoded by this gene belongs to the family of X-pro-aminopeptidases that utilize a metal cofactor, and remove the N-terminal amino acid from peptides with a proline residue in the penultimate position. This protein has been shown to localize to the mitochondria of renal cells, and have a role in ciliary function. Mutations in this gene are associated with nephronophthisis-like nephropathy-1. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene, however, expression of some of these isoforms in vivo is not known.[provided by RefSeq, Mar 2011]","start":40857077,"end":40932815,"strand":1,"description":"X-prolyl aminopeptidase 3 [Source:HGNC Symbol;Acc:HGNC:28052]"}, {"versioned_ensembl_gene_id":"ENSG00000174796.12","gene_symbol":"THAP6","gene_name":"THAP domain containing 6 [Source:HGNC Symbol;Acc:HGNC:23189]","synonyms":"MGC30052","biotype":"protein_coding","ncbi_id":"152815","summary":null,"start":75513946,"end":75550473,"strand":1,"description":"THAP domain containing 6 [Source:HGNC Symbol;Acc:HGNC:23189]"}, {"versioned_ensembl_gene_id":"ENSG00000215094.3","gene_symbol":"AL583835.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149951833,"end":149952239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228800.1","gene_symbol":"AL590068.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30553854,"end":30554483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250945.1","gene_symbol":"AC096773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127043430,"end":127077762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255394.4","gene_symbol":"C8orf49","gene_name":"chromosome 8 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:32200]","synonyms":"G4DM,FLJ30972","biotype":"lincRNA","ncbi_id":"606553","summary":null,"start":11761256,"end":11763223,"strand":1,"description":"chromosome 8 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:32200]"}, {"versioned_ensembl_gene_id":"ENSG00000236178.9","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"VARS2L,DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30898107,"end":30916176,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000163026.11","gene_symbol":"WDCP","gene_name":"WD repeat and coiled coil containing [Source:HGNC Symbol;Acc:HGNC:26157]","synonyms":"FLJ21945,C2orf44","biotype":"protein_coding","ncbi_id":"80304","summary":null,"start":24029340,"end":24049575,"strand":-1,"description":"WD repeat and coiled coil containing [Source:HGNC Symbol;Acc:HGNC:26157]"}, {"versioned_ensembl_gene_id":"ENSG00000248138.5","gene_symbol":"AC097515.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16400430,"end":16512187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276879.2","gene_symbol":"IFI27L2","gene_name":"interferon alpha inducible protein 27 like 2 [Source:HGNC Symbol;Acc:HGNC:19753]","synonyms":"TLH29,FAM14A","biotype":"protein_coding","ncbi_id":"83982","summary":null,"start":94127779,"end":94130253,"strand":-1,"description":"interferon alpha inducible protein 27 like 2 [Source:HGNC Symbol;Acc:HGNC:19753]"}, {"versioned_ensembl_gene_id":"ENSG00000275882.1","gene_symbol":"IKBKGP1","gene_name":"inhibitor of nuclear factor kappa B kinase subunit gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24455]","synonyms":"IKBKGP,deltaNEMO","biotype":"unprocessed_pseudogene","ncbi_id":"246210","summary":null,"start":154639978,"end":154648275,"strand":-1,"description":"inhibitor of nuclear factor kappa B kinase subunit gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24455]"}, {"versioned_ensembl_gene_id":"ENSG00000178201.4","gene_symbol":"VN1R1","gene_name":"vomeronasal 1 receptor 1 [Source:HGNC Symbol;Acc:HGNC:13548]","synonyms":"ZVNR1,ZVNH1,VNR19I1,V1RL1","biotype":"protein_coding","ncbi_id":"57191","summary":"Pheromones are chemical signals that elicit specific behavioral responses and physiologic alterations in recipients of the same species. The protein encoded by this gene is similar to pheromone receptors and is primarily localized to the olfactory mucosa. An alternate splice variant of this gene is thought to exist, but its full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":57454790,"end":57457142,"strand":-1,"description":"vomeronasal 1 receptor 1 [Source:HGNC Symbol;Acc:HGNC:13548]"}, {"versioned_ensembl_gene_id":"ENSG00000260924.2","gene_symbol":"LINC01311","gene_name":"long intergenic non-protein coding RNA 1311 [Source:HGNC Symbol;Acc:HGNC:50503]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652736","summary":null,"start":19171395,"end":19172839,"strand":1,"description":"long intergenic non-protein coding RNA 1311 [Source:HGNC Symbol;Acc:HGNC:50503]"}, {"versioned_ensembl_gene_id":"ENSG00000170296.9","gene_symbol":"GABARAP","gene_name":"GABA type A receptor-associated protein [Source:HGNC Symbol;Acc:HGNC:4067]","synonyms":"MM46,ATG8A","biotype":"protein_coding","ncbi_id":"11337","summary":"Gamma-aminobutyric acid A receptors [GABA(A) receptors] are ligand-gated chloride channels that mediate inhibitory neurotransmission. This gene encodes GABA(A) receptor-associated protein, which is highly positively charged in its N-terminus and shares sequence similarity with light chain-3 of microtubule-associated proteins 1A and 1B. This protein clusters neurotransmitter receptors by mediating interaction with the cytoskeleton. [provided by RefSeq, Jul 2008]","start":7240014,"end":7242770,"strand":-1,"description":"GABA type A receptor-associated protein [Source:HGNC Symbol;Acc:HGNC:4067]"}, {"versioned_ensembl_gene_id":"ENSG00000234863.1","gene_symbol":"AC096644.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220455154,"end":220455312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213964.3","gene_symbol":"CHCHD4P4","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44492]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728143","summary":null,"start":11234256,"end":11234582,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44492]"}, {"versioned_ensembl_gene_id":"ENSG00000112992.16","gene_symbol":"NNT","gene_name":"nicotinamide nucleotide transhydrogenase [Source:HGNC Symbol;Acc:HGNC:7863]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23530","summary":"This gene encodes an integral protein of the inner mitochondrial membrane. The enzyme couples hydride transfer between NAD(H) and NADP(+) to proton translocation across the inner mitochondrial membrane. Under most physiological conditions, the enzyme uses energy from the mitochondrial proton gradient to produce high concentrations of NADPH. The resulting NADPH is used for biosynthesis and in free radical detoxification. [provided by RefSeq, Sep 2016]","start":43602692,"end":43707405,"strand":1,"description":"nicotinamide nucleotide transhydrogenase [Source:HGNC Symbol;Acc:HGNC:7863]"}, {"versioned_ensembl_gene_id":"ENSG00000172478.17","gene_symbol":"C2orf54","gene_name":"chromosome 2 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26216]","synonyms":"FLJ22671","biotype":"protein_coding","ncbi_id":"79919","summary":null,"start":240886048,"end":240896889,"strand":-1,"description":"chromosome 2 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26216]"}, {"versioned_ensembl_gene_id":"ENSG00000186469.8","gene_symbol":"GNG2","gene_name":"G protein subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:4404]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54331","summary":"This gene encodes one of the gamma subunits of a guanine nucleotide-binding protein. Such proteins are involved in signaling mechanisms across membranes. Various subunits forms heterodimers which then interact with the different signal molecules. [provided by RefSeq, Aug 2011]","start":51826195,"end":51979342,"strand":1,"description":"G protein subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:4404]"}, {"versioned_ensembl_gene_id":"ENSG00000258928.1","gene_symbol":"AL358333.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51916145,"end":51918571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248092.7","gene_symbol":"NNT-AS1","gene_name":"NNT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49005]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652772","summary":null,"start":43571594,"end":43603230,"strand":-1,"description":"NNT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49005]"}, {"versioned_ensembl_gene_id":"ENSG00000220069.1","gene_symbol":"RPL7P27","gene_name":"ribosomal protein L7 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643906","summary":null,"start":86086415,"end":86087134,"strand":-1,"description":"ribosomal protein L7 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36649]"}, {"versioned_ensembl_gene_id":"ENSG00000232287.2","gene_symbol":"SLC6A1-AS1","gene_name":"SLC6A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40546]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874090","summary":null,"start":11006098,"end":11019224,"strand":-1,"description":"SLC6A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40546]"}, {"versioned_ensembl_gene_id":"ENSG00000138193.15","gene_symbol":"PLCE1","gene_name":"phospholipase C epsilon 1 [Source:HGNC Symbol;Acc:HGNC:17175]","synonyms":"PLCE,NPHS3,KIAA1516","biotype":"protein_coding","ncbi_id":"51196","summary":"This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]","start":94030812,"end":94332823,"strand":1,"description":"phospholipase C epsilon 1 [Source:HGNC Symbol;Acc:HGNC:17175]"}, {"versioned_ensembl_gene_id":"ENSG00000214943.4","gene_symbol":"GPR33","gene_name":"G protein-coupled receptor 33 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4489]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2856","summary":"This gene has been identified as an orphan chemoattractant G-protein-coupled receptors (GPCR) pseudogene. Studies have shown that the inactivated gene is present as the predominant allele in the human population. A small fraction of the human population has been found to harbor an intact allele.[provided by RefSeq, Oct 2010]","start":31482875,"end":31488142,"strand":-1,"description":"G protein-coupled receptor 33 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4489]"}, {"versioned_ensembl_gene_id":"ENSG00000257443.1","gene_symbol":"AC068305.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58920639,"end":59064238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130508.10","gene_symbol":"PXDN","gene_name":"peroxidasin [Source:HGNC Symbol;Acc:HGNC:14966]","synonyms":"PXN,PRG2,MG50,KIAA0230,D2S448E,D2S448","biotype":"protein_coding","ncbi_id":"7837","summary":"This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis. [provided by RefSeq, Aug 2014]","start":1631887,"end":1744852,"strand":-1,"description":"peroxidasin [Source:HGNC Symbol;Acc:HGNC:14966]"}, {"versioned_ensembl_gene_id":"ENSG00000257288.1","gene_symbol":"AC068305.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59052980,"end":59054184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256139.2","gene_symbol":"AC007637.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":109111218,"end":109125594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074276.10","gene_symbol":"CDHR2","gene_name":"cadherin related family member 2 [Source:HGNC Symbol;Acc:HGNC:18231]","synonyms":"PCLKC,PCDH24,PC-LKC,FLJ20383,FLJ20124","biotype":"protein_coding","ncbi_id":"54825","summary":"This gene is a member of the protocadherin family, which represents a subset of the larger cadherin superfamily. The members of the protocadherin family encode non-classical cadherins that function as calcium-dependent cell-cell adhesion molecules. This protocadherin represents a new candidate for tumor suppression. Alternatively spliced transcript variants that encode the same protein have been identified. [provided by RefSeq, Jan 2010]","start":176542511,"end":176595974,"strand":1,"description":"cadherin related family member 2 [Source:HGNC Symbol;Acc:HGNC:18231]"}, {"versioned_ensembl_gene_id":"ENSG00000186288.5","gene_symbol":"PABPC1L2A","gene_name":"poly(A) binding protein cytoplasmic 1 like 2A [Source:HGNC Symbol;Acc:HGNC:27989]","synonyms":"RBM32A","biotype":"protein_coding","ncbi_id":"340529","summary":null,"start":73077276,"end":73079512,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 like 2A [Source:HGNC Symbol;Acc:HGNC:27989]"}, {"versioned_ensembl_gene_id":"ENSG00000226725.2","gene_symbol":"PABPC1L2B-AS1","gene_name":"PABPC1L2B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50345]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928345","summary":null,"start":72998388,"end":73002856,"strand":-1,"description":"PABPC1L2B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50345]"}, {"versioned_ensembl_gene_id":"ENSG00000108578.14","gene_symbol":"BLMH","gene_name":"bleomycin hydrolase [Source:HGNC Symbol;Acc:HGNC:1059]","synonyms":"BH","biotype":"protein_coding","ncbi_id":"642","summary":"Bleomycin hydrolase (BMH) is a cytoplasmic cysteine peptidase that is highly conserved through evolution; however, the only known activity of the enzyme is metabolic inactivation of the glycopeptide bleomycin (BLM), an essential component of combination chemotherapy regimens for cancer. The protein contains the signature active site residues of the cysteine protease papain superfamily. [provided by RefSeq, Jul 2008]","start":30248195,"end":30292056,"strand":-1,"description":"bleomycin hydrolase [Source:HGNC Symbol;Acc:HGNC:1059]"}, {"versioned_ensembl_gene_id":"ENSG00000189077.10","gene_symbol":"TMEM120A","gene_name":"transmembrane protein 120A [Source:HGNC Symbol;Acc:HGNC:21697]","synonyms":"TMPIT,NET29","biotype":"protein_coding","ncbi_id":"83862","summary":null,"start":75986837,"end":75994659,"strand":-1,"description":"transmembrane protein 120A [Source:HGNC Symbol;Acc:HGNC:21697]"}, {"versioned_ensembl_gene_id":"ENSG00000165181.16","gene_symbol":"C9orf84","gene_name":"chromosome 9 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:26535]","synonyms":"FLJ32779","biotype":"protein_coding","ncbi_id":"158401","summary":null,"start":111686173,"end":111795008,"strand":-1,"description":"chromosome 9 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:26535]"}, {"versioned_ensembl_gene_id":"ENSG00000251258.1","gene_symbol":"RFPL4B","gene_name":"ret finger protein like 4B [Source:HGNC Symbol;Acc:HGNC:33264]","synonyms":"RNF211","biotype":"protein_coding","ncbi_id":"442247","summary":null,"start":112347330,"end":112351296,"strand":1,"description":"ret finger protein like 4B [Source:HGNC Symbol;Acc:HGNC:33264]"}, {"versioned_ensembl_gene_id":"ENSG00000270812.1","gene_symbol":"AC002069.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88455309,"end":88456191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225701.1","gene_symbol":"EIF4A1P13","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37934]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462826","summary":null,"start":88448788,"end":88449017,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37934]"}, {"versioned_ensembl_gene_id":"ENSG00000243264.2","gene_symbol":"IGKV2D-29","gene_name":"immunoglobulin kappa variable 2D-29 [Source:HGNC Symbol;Acc:HGNC:5800]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28882","summary":null,"start":89947512,"end":89948279,"strand":1,"description":"immunoglobulin kappa variable 2D-29 [Source:HGNC Symbol;Acc:HGNC:5800]"}, {"versioned_ensembl_gene_id":"ENSG00000229597.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTN7,HSBLMHC1,BTL-II,HSBLMHC1,BTL-II,BTN7","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32351409,"end":32364583,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000228738.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32347957,"end":32351132,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000214141.4","gene_symbol":"ACTN4P2","gene_name":"actinin alpha 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391026","summary":null,"start":37776670,"end":37779418,"strand":1,"description":"actinin alpha 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44032]"}, {"versioned_ensembl_gene_id":"ENSG00000147526.19","gene_symbol":"TACC1","gene_name":"transforming acidic coiled-coil containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6867","summary":"This locus may represent a breast cancer candidate gene. It is located close to FGFR1 on a region of chromosome 8 that is amplified in some breast cancers. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2017]","start":38728186,"end":38853028,"strand":1,"description":"transforming acidic coiled-coil containing protein 1 [Source:HGNC Symbol;Acc:HGNC:11522]"}, {"versioned_ensembl_gene_id":"ENSG00000232531.3","gene_symbol":"AC027612.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91747940,"end":91748986,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217585.1","gene_symbol":"AL021407.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16107622,"end":16108593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126767.17","gene_symbol":"ELK1","gene_name":"ELK1, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3321]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2002","summary":"This gene is a member of the Ets family of transcription factors and of the ternary complex factor (TCF) subfamily. Proteins of the TCF subfamily form a ternary complex by binding to the the serum response factor and the serum response element in the promoter of the c-fos proto-oncogene. The protein encoded by this gene is a nuclear target for the ras-raf-MAPK signaling cascade. This gene produces multiple isoforms by using alternative translational start codons and by alternative splicing. Related pseudogenes have been identified on chromosomes 7 and 14. [provided by RefSeq, Mar 2012]","start":47635521,"end":47650604,"strand":-1,"description":"ELK1, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3321]"}, {"versioned_ensembl_gene_id":"ENSG00000229684.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30798683,"end":30803908,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000254802.1","gene_symbol":"AC022182.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60965802,"end":60967775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250183.2","gene_symbol":"AC097173.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":119937557,"end":119963898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233323.10","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"XB,TNXB2,XBS,TNXB1,TNXBS","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31989596,"end":32066062,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000211739.4","gene_symbol":"TRBV12-2","gene_name":"T-cell receptor beta variable 12-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12184]","synonyms":"TRBV122,TCRBV8S5P,TCRBV12S2","biotype":"TR_V_pseudogene","ncbi_id":"28578","summary":null,"start":142440883,"end":142441325,"strand":1,"description":"T-cell receptor beta variable 12-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12184]"}, {"versioned_ensembl_gene_id":"ENSG00000220581.1","gene_symbol":"VN1R12P","gene_name":"vomeronasal 1 receptor 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:18722]","synonyms":"VNR6I3P,hs6V1-3p,bA373D17.2","biotype":"unitary_pseudogene","ncbi_id":"387321","summary":null,"start":27033435,"end":27034310,"strand":-1,"description":"vomeronasal 1 receptor 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:18722]"}, {"versioned_ensembl_gene_id":"ENSG00000144366.15","gene_symbol":"GULP1","gene_name":"GULP, engulfment adaptor PTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18649]","synonyms":"GULP,CED6,CED-6","biotype":"protein_coding","ncbi_id":"51454","summary":"The protein encoded by this gene is an adapter protein necessary for the engulfment of apoptotic cells by phagocytes. Several transcript variants, some protein coding and some thought not to be protein coding, have been found for this gene. [provided by RefSeq, Nov 2011]","start":188291669,"end":188595931,"strand":1,"description":"GULP, engulfment adaptor PTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18649]"}, {"versioned_ensembl_gene_id":"ENSG00000164056.10","gene_symbol":"SPRY1","gene_name":"sprouty RTK signaling antagonist 1 [Source:HGNC Symbol;Acc:HGNC:11269]","synonyms":"hSPRY1","biotype":"protein_coding","ncbi_id":"10252","summary":null,"start":123396795,"end":123403760,"strand":1,"description":"sprouty RTK signaling antagonist 1 [Source:HGNC Symbol;Acc:HGNC:11269]"}, {"versioned_ensembl_gene_id":"ENSG00000270593.1","gene_symbol":"AC073333.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16849957,"end":16850725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132874.14","gene_symbol":"SLC14A2","gene_name":"solute carrier family 14 member 2 [Source:HGNC Symbol;Acc:HGNC:10919]","synonyms":"UT2,HUT2","biotype":"protein_coding","ncbi_id":"8170","summary":"The protein encoded by this gene belongs to the urea transporter family. In mammalian cells, urea is the chief end product of nitrogen catabolism, and plays an important role in the urinary concentration mechanism. This protein is expressed in the inner medulla of the kidney, and mediates rapid transepithelial urea transport across the inner medullary collecting duct. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2011]","start":45212995,"end":45683686,"strand":1,"description":"solute carrier family 14 member 2 [Source:HGNC Symbol;Acc:HGNC:10919]"}, {"versioned_ensembl_gene_id":"ENSG00000282822.1","gene_symbol":"AC242528.2","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106774973,"end":106775426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257042.1","gene_symbol":"AC008011.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27958517,"end":27969813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237048.2","gene_symbol":"TTTY12","gene_name":"testis-specific transcript, Y-linked 12 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18493]","synonyms":"TTY11,NCRNA00135","biotype":"lincRNA","ncbi_id":"83867","summary":null,"start":7804924,"end":7810683,"strand":1,"description":"testis-specific transcript, Y-linked 12 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18493]"}, {"versioned_ensembl_gene_id":"ENSG00000177465.4","gene_symbol":"ACOT4","gene_name":"acyl-CoA thioesterase 4 [Source:HGNC Symbol;Acc:HGNC:19748]","synonyms":"PTE2B,PTE-Ib,FLJ31235","biotype":"protein_coding","ncbi_id":"122970","summary":null,"start":73591706,"end":73596496,"strand":1,"description":"acyl-CoA thioesterase 4 [Source:HGNC Symbol;Acc:HGNC:19748]"}, {"versioned_ensembl_gene_id":"ENSG00000242198.1","gene_symbol":"AC008897.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75374463,"end":75374809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176853.15","gene_symbol":"FAM91A1","gene_name":"family with sequence similarity 91 member A1 [Source:HGNC Symbol;Acc:HGNC:26306]","synonyms":"FLJ23790","biotype":"protein_coding","ncbi_id":"157769","summary":null,"start":123768456,"end":123815452,"strand":1,"description":"family with sequence similarity 91 member A1 [Source:HGNC Symbol;Acc:HGNC:26306]"}, {"versioned_ensembl_gene_id":"ENSG00000234415.1","gene_symbol":"RPL5P7","gene_name":"ribosomal protein L5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36583]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344178","summary":null,"start":173871653,"end":173872465,"strand":-1,"description":"ribosomal protein L5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36583]"}, {"versioned_ensembl_gene_id":"ENSG00000265356.2","gene_symbol":"AC004147.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":33935437,"end":34156000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263435.1","gene_symbol":"AC024610.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33976531,"end":33980851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264990.1","gene_symbol":"AC005549.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34176538,"end":34178166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168056.15","gene_symbol":"LTBP3","gene_name":"latent transforming growth factor beta binding protein 3 [Source:HGNC Symbol;Acc:HGNC:6716]","synonyms":"LTBP2","biotype":"protein_coding","ncbi_id":"4054","summary":"The protein encoded by this gene forms a complex with transforming growth factor beta (TGF-beta) proteins and may be involved in their subcellular localization. Activation of this complex requires removal of the encoded binding protein. This protein also may play a structural role in the extracellular matrix. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]","start":65538805,"end":65558930,"strand":-1,"description":"latent transforming growth factor beta binding protein 3 [Source:HGNC Symbol;Acc:HGNC:6716]"}, {"versioned_ensembl_gene_id":"ENSG00000220563.1","gene_symbol":"PKMP3","gene_name":"pyruvate kinase, muscle pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44245]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419758","summary":null,"start":85659892,"end":85660606,"strand":-1,"description":"pyruvate kinase, muscle pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44245]"}, {"versioned_ensembl_gene_id":"ENSG00000150347.14","gene_symbol":"ARID5B","gene_name":"AT-rich interaction domain 5B [Source:HGNC Symbol;Acc:HGNC:17362]","synonyms":"MRF2,FLJ21150","biotype":"protein_coding","ncbi_id":"84159","summary":"This gene encodes a member of the AT-rich interaction domain (ARID) family of DNA binding proteins. The encoded protein forms a histone H3K9Me2 demethylase complex with PHD finger protein 2 and regulates the transcription of target genes involved in adipogenesis and liver development. This gene also plays a role in cell growth and differentiation of B-lymphocyte progenitors, and single nucleotide polymorphisms in this gene are associated with acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":61901300,"end":62096944,"strand":1,"description":"AT-rich interaction domain 5B [Source:HGNC Symbol;Acc:HGNC:17362]"}, {"versioned_ensembl_gene_id":"ENSG00000234650.5","gene_symbol":"PCCA-AS1","gene_name":"PCCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39901]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885777","summary":null,"start":100464440,"end":100481157,"strand":-1,"description":"PCCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39901]"}, {"versioned_ensembl_gene_id":"ENSG00000122012.13","gene_symbol":"SV2C","gene_name":"synaptic vesicle glycoprotein 2C [Source:HGNC Symbol;Acc:HGNC:30670]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22987","summary":null,"start":76083172,"end":76353939,"strand":1,"description":"synaptic vesicle glycoprotein 2C [Source:HGNC Symbol;Acc:HGNC:30670]"}, {"versioned_ensembl_gene_id":"ENSG00000221869.4","gene_symbol":"CEBPD","gene_name":"CCAAT/enhancer binding protein delta [Source:HGNC Symbol;Acc:HGNC:1835]","synonyms":"NF-IL6-beta,CRP3,CELF,C/EBP-delta","biotype":"protein_coding","ncbi_id":"1052","summary":"The protein encoded by this intronless gene is a bZIP transcription factor which can bind as a homodimer to certain DNA regulatory regions. It can also form heterodimers with the related protein CEBP-alpha. The encoded protein is important in the regulation of genes involved in immune and inflammatory responses, and may be involved in the regulation of genes associated with activation and/or differentiation of macrophages. The cytogenetic location of this locus has been reported as both 8p11 and 8q11. [provided by RefSeq, Sep 2010]","start":47736909,"end":47739086,"strand":-1,"description":"CCAAT/enhancer binding protein delta [Source:HGNC Symbol;Acc:HGNC:1835]"}, {"versioned_ensembl_gene_id":"ENSG00000279021.1","gene_symbol":"AC092139.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81463892,"end":81464859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250990.1","gene_symbol":"AC098851.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77246340,"end":77258123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279841.1","gene_symbol":"AC092135.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81630193,"end":81632038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148572.15","gene_symbol":"NRBF2","gene_name":"nuclear receptor binding factor 2 [Source:HGNC Symbol;Acc:HGNC:19692]","synonyms":"FLJ30395,DKFZp564C1664,COPR2,COPR1","biotype":"protein_coding","ncbi_id":"29982","summary":null,"start":63133247,"end":63155031,"strand":1,"description":"nuclear receptor binding factor 2 [Source:HGNC Symbol;Acc:HGNC:19692]"}, {"versioned_ensembl_gene_id":"ENSG00000261459.1","gene_symbol":"AC002310.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30525923,"end":30534852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282528.1","gene_symbol":"AC246789.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16629420,"end":16630050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230806.1","gene_symbol":"SRGAP2-AS1","gene_name":"SRGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40902]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873165","summary":null,"start":121360156,"end":121398806,"strand":-1,"description":"SRGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40902]"}, {"versioned_ensembl_gene_id":"ENSG00000146232.15","gene_symbol":"NFKBIE","gene_name":"NFKB inhibitor epsilon [Source:HGNC Symbol;Acc:HGNC:7799]","synonyms":"IKBE","biotype":"protein_coding","ncbi_id":"4794","summary":"The protein encoded by this gene binds to components of NF-kappa-B, trapping the complex in the cytoplasm and preventing it from activating genes in the nucleus. Phosphorylation of the encoded protein targets it for destruction by the ubiquitin pathway, which activates NF-kappa-B by making it available to translocate to the nucleus. [provided by RefSeq, Sep 2011]","start":44258166,"end":44265788,"strand":-1,"description":"NFKB inhibitor epsilon [Source:HGNC Symbol;Acc:HGNC:7799]"}, {"versioned_ensembl_gene_id":"ENSG00000241350.1","gene_symbol":"PMS2P11","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:9125]","synonyms":"PMSR6,PMS2L11","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107161145","summary":null,"start":77011551,"end":77015853,"strand":1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:9125]"}, {"versioned_ensembl_gene_id":"ENSG00000282383.1","gene_symbol":"IGHV3-54","gene_name":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28419","summary":null,"start":106626027,"end":106626473,"strand":-1,"description":"immunoglobulin heavy variable 3-54 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5611]"}, {"versioned_ensembl_gene_id":"ENSG00000262322.1","gene_symbol":"MTND4P34","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:51948]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075308","summary":null,"start":10721698,"end":10723068,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:51948]"}, {"versioned_ensembl_gene_id":"ENSG00000258628.1","gene_symbol":"AC126603.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20228620,"end":20277503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198610.10","gene_symbol":"AKR1C4","gene_name":"aldo-keto reductase family 1 member C4 [Source:HGNC Symbol;Acc:HGNC:387]","synonyms":"CDR,C11,3-alpha-HSD,MGC22581,HAKRA,DD4,CHDR","biotype":"protein_coding","ncbi_id":"1109","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme catalyzes the bioreduction of chlordecone, a toxic organochlorine pesticide, to chlordecone alcohol in liver. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. [provided by RefSeq, Jul 2008]","start":5195462,"end":5218949,"strand":1,"description":"aldo-keto reductase family 1 member C4 [Source:HGNC Symbol;Acc:HGNC:387]"}, {"versioned_ensembl_gene_id":"ENSG00000229348.1","gene_symbol":"HYI-AS1","gene_name":"HYI antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41173]","synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":"100873923","summary":null,"start":43453927,"end":43456995,"strand":1,"description":"HYI antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41173]"}, {"versioned_ensembl_gene_id":"ENSG00000213343.5","gene_symbol":"RPL21P18","gene_name":"ribosomal protein L21 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:28362]","synonyms":"ENSG00000184796","biotype":"processed_pseudogene","ncbi_id":"729484","summary":null,"start":66037235,"end":66037714,"strand":1,"description":"ribosomal protein L21 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:28362]"}, {"versioned_ensembl_gene_id":"ENSG00000255727.1","gene_symbol":"LINC01489","gene_name":"long intergenic non-protein coding RNA 1489 [Source:HGNC Symbol;Acc:HGNC:51145]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928340","summary":null,"start":15001833,"end":15006683,"strand":1,"description":"long intergenic non-protein coding RNA 1489 [Source:HGNC Symbol;Acc:HGNC:51145]"}, {"versioned_ensembl_gene_id":"ENSG00000197165.10","gene_symbol":"SULT1A2","gene_name":"sulfotransferase family 1A member 2 [Source:HGNC Symbol;Acc:HGNC:11454]","synonyms":"STP2,HAST4","biotype":"protein_coding","ncbi_id":"6799","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes one of two phenol sulfotransferases with thermostable enzyme activity. Two alternatively spliced variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]","start":28591943,"end":28597109,"strand":-1,"description":"sulfotransferase family 1A member 2 [Source:HGNC Symbol;Acc:HGNC:11454]"}, {"versioned_ensembl_gene_id":"ENSG00000119547.5","gene_symbol":"ONECUT2","gene_name":"one cut homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8139]","synonyms":"OC-2","biotype":"protein_coding","ncbi_id":"9480","summary":"This gene encodes a member of the onecut family of transcription factors, which are characterized by a cut domain and an atypical homeodomain. The protein binds to specific DNA sequences and stimulates expression of target genes, including genes involved in melanocyte and hepatocyte differentiation. [provided by RefSeq, Jul 2008]","start":57435685,"end":57491297,"strand":1,"description":"one cut homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8139]"}, {"versioned_ensembl_gene_id":"ENSG00000241910.5","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32846263,"end":32850548,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000004142.11","gene_symbol":"POLDIP2","gene_name":"DNA polymerase delta interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23781]","synonyms":"PDIP38,DKFZP586F1524","biotype":"protein_coding","ncbi_id":"26073","summary":"This gene encodes a protein that interacts with the DNA polymerase delta p50 subunit, as well as with proliferating cell nuclear antigen. The encoded protein maybe play a role in the ability of the replication fork to bypass DNA lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":28347177,"end":28357522,"strand":-1,"description":"DNA polymerase delta interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23781]"}, {"versioned_ensembl_gene_id":"ENSG00000271322.1","gene_symbol":"AL357312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98348451,"end":98348748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236397.3","gene_symbol":"DDX11L2","gene_name":"DEAD/H-box helicase 11 like 2 [Source:HGNC Symbol;Acc:HGNC:37103]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"84771","summary":null,"start":113599036,"end":113601261,"strand":-1,"description":"DEAD/H-box helicase 11 like 2 [Source:HGNC Symbol;Acc:HGNC:37103]"}, {"versioned_ensembl_gene_id":"ENSG00000276223.1","gene_symbol":"AL118522.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44746642,"end":44747201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126858.16","gene_symbol":"RHOT1","gene_name":"ras homolog family member T1 [Source:HGNC Symbol;Acc:HGNC:21168]","synonyms":"FLJ11040,ARHT1,MIRO-1","biotype":"protein_coding","ncbi_id":"55288","summary":null,"start":32142454,"end":32253374,"strand":1,"description":"ras homolog family member T1 [Source:HGNC Symbol;Acc:HGNC:21168]"}, {"versioned_ensembl_gene_id":"ENSG00000176294.5","gene_symbol":"OR4N2","gene_name":"olfactory receptor family 4 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:14742]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390429","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a seven-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Mar 2014]","start":19719015,"end":19830253,"strand":1,"description":"olfactory receptor family 4 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:14742]"}, {"versioned_ensembl_gene_id":"ENSG00000258292.1","gene_symbol":"LINC02410","gene_name":"long intergenic non-protein coding RNA 2410 [Source:HGNC Symbol;Acc:HGNC:53339]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369920","summary":null,"start":95803097,"end":95823307,"strand":1,"description":"long intergenic non-protein coding RNA 2410 [Source:HGNC Symbol;Acc:HGNC:53339]"}, {"versioned_ensembl_gene_id":"ENSG00000278270.4","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201357,"end":54249609,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000272506.1","gene_symbol":"AL357078.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65003470,"end":65004087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249263.2","gene_symbol":"PARP4P3","gene_name":"poly(ADP-ribose) polymerase family member 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:274]","synonyms":"ADPRTL4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107133524","summary":null,"start":16653892,"end":16659628,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:274]"}, {"versioned_ensembl_gene_id":"ENSG00000263797.1","gene_symbol":"AP005210.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6873399,"end":6875024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228808.1","gene_symbol":"HMGB3P4","gene_name":"high mobility group box 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39104]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873890","summary":null,"start":99372173,"end":99372686,"strand":1,"description":"high mobility group box 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39104]"}, {"versioned_ensembl_gene_id":"ENSG00000156017.12","gene_symbol":"CARNMT1","gene_name":"carnosine N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23435]","synonyms":"FLJ25795,C9orf41","biotype":"protein_coding","ncbi_id":"138199","summary":"The protein encoded by this gene is a methyltransferase that converts carnosine to anserine, a dipeptide found abundantly in skeletal muscle. The encoded protein can methylate other dipeptides as well. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":74981020,"end":75028423,"strand":-1,"description":"carnosine N-methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23435]"}, {"versioned_ensembl_gene_id":"ENSG00000089159.16","gene_symbol":"PXN","gene_name":"paxillin [Source:HGNC Symbol;Acc:HGNC:9718]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5829","summary":"This gene encodes a cytoskeletal protein involved in actin-membrane attachment at sites of cell adhesion to the extracellular matrix (focal adhesion). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. These isoforms exhibit different expression pattern, and have different biochemical, as well as physiological properties (PMID:9054445). [provided by RefSeq, Aug 2011]","start":120210439,"end":120265771,"strand":-1,"description":"paxillin [Source:HGNC Symbol;Acc:HGNC:9718]"}, {"versioned_ensembl_gene_id":"ENSG00000281833.1","gene_symbol":"AL354892.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":169770413,"end":169772042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114902.13","gene_symbol":"SPCS1","gene_name":"signal peptidase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23401]","synonyms":"YJR010C-A,SPC12,SPC1,HSPC033","biotype":"protein_coding","ncbi_id":"28972","summary":null,"start":52704955,"end":52711146,"strand":1,"description":"signal peptidase complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:23401]"}, {"versioned_ensembl_gene_id":"ENSG00000204248.10","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"DFNB53,DFNA13,HKE5","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33162681,"end":33192499,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000265378.1","gene_symbol":"AC012572.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78505165,"end":78506410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266273.1","gene_symbol":"AC044873.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78795612,"end":78796672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283585.1","gene_symbol":"AC002384.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106824883,"end":106838476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228742.9","gene_symbol":"AC002384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106775011,"end":106795564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249909.1","gene_symbol":"CYCTP","gene_name":"cytochrome c, testis, pseudogene [Source:HGNC Symbol;Acc:HGNC:24424]","synonyms":"HCP9","biotype":"unitary_pseudogene","ncbi_id":"360163","summary":null,"start":178092503,"end":178104470,"strand":-1,"description":"cytochrome c, testis, pseudogene [Source:HGNC Symbol;Acc:HGNC:24424]"}, {"versioned_ensembl_gene_id":"ENSG00000282613.1","gene_symbol":"AC067930.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143573490,"end":143577397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265843.2","gene_symbol":"LINC01029","gene_name":"long intergenic non-protein coding RNA 1029 [Source:HGNC Symbol;Acc:HGNC:49015]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927715","summary":null,"start":77971294,"end":77993722,"strand":-1,"description":"long intergenic non-protein coding RNA 1029 [Source:HGNC Symbol;Acc:HGNC:49015]"}, {"versioned_ensembl_gene_id":"ENSG00000276187.4","gene_symbol":"ERMARD","gene_name":"ER membrane associated RNA degradation [Source:HGNC Symbol;Acc:HGNC:21056]","synonyms":"FLJ11152,dJ266L20.3,C6orf70","biotype":"protein_coding","ncbi_id":"55780","summary":"The protein encoded by this gene contains 2 transmembrane domains near the C-terminus and is localized in the endoplasmic reticulum. Knockout of this gene in developing rat brain showed that it may be involved in neuronal migration. Mutations in this gene are associated with periventricular nodular heterotopia-6 (PVNH6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]","start":169751622,"end":169781584,"strand":1,"description":"ER membrane associated RNA degradation [Source:HGNC Symbol;Acc:HGNC:21056]"}, {"versioned_ensembl_gene_id":"ENSG00000253276.2","gene_symbol":"CCDC71L","gene_name":"coiled-coil domain containing 71 like [Source:HGNC Symbol;Acc:HGNC:26685]","synonyms":"FLJ36031,C7orf74","biotype":"protein_coding","ncbi_id":"168455","summary":null,"start":106656765,"end":106660996,"strand":-1,"description":"coiled-coil domain containing 71 like [Source:HGNC Symbol;Acc:HGNC:26685]"}, {"versioned_ensembl_gene_id":"ENSG00000235552.4","gene_symbol":"AP005202.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":6462144,"end":6463015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155849.15","gene_symbol":"ELMO1","gene_name":"engulfment and cell motility 1 [Source:HGNC Symbol;Acc:HGNC:16286]","synonyms":"CED-12,KIAA0281,ELMO-1,CED12","biotype":"protein_coding","ncbi_id":"9844","summary":"This gene encodes a member of the engulfment and cell motility protein family. These proteins interact with dedicator of cytokinesis proteins to promote phagocytosis and cell migration. Increased expression of this gene and dedicator of cytokinesis 1 may promote glioma cell invasion, and single nucleotide polymorphisms in this gene may be associated with diabetic nephropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":36854361,"end":37449249,"strand":-1,"description":"engulfment and cell motility 1 [Source:HGNC Symbol;Acc:HGNC:16286]"}, {"versioned_ensembl_gene_id":"ENSG00000224101.1","gene_symbol":"ELMO1-AS1","gene_name":"ELMO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40765]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861514","summary":null,"start":36997796,"end":37013630,"strand":1,"description":"ELMO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40765]"}, {"versioned_ensembl_gene_id":"ENSG00000213744.3","gene_symbol":"RPS10P14","gene_name":"ribosomal protein S10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35880]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646942","summary":null,"start":37375522,"end":37376023,"strand":1,"description":"ribosomal protein S10 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35880]"}, {"versioned_ensembl_gene_id":"ENSG00000256093.1","gene_symbol":"AC122688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125056359,"end":125056581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251081.1","gene_symbol":"AC104663.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107258700,"end":107301870,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281973.1","gene_symbol":"IGHV3-37","gene_name":"immunoglobulin heavy variable 3-37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5600]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28430","summary":null,"start":106421357,"end":106421795,"strand":-1,"description":"immunoglobulin heavy variable 3-37 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5600]"}, {"versioned_ensembl_gene_id":"ENSG00000282104.1","gene_symbol":"IGHV3-35","gene_name":"immunoglobulin heavy variable 3-35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5598]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28432","summary":null,"start":106414071,"end":106414539,"strand":-1,"description":"immunoglobulin heavy variable 3-35 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5598]"}, {"versioned_ensembl_gene_id":"ENSG00000235636.1","gene_symbol":"NUS1P1","gene_name":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38472]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729148","summary":null,"start":47512602,"end":47513483,"strand":-1,"description":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38472]"}, {"versioned_ensembl_gene_id":"ENSG00000213563.6","gene_symbol":"C8orf82","gene_name":"chromosome 8 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:33826]","synonyms":"MGC70857","biotype":"protein_coding","ncbi_id":"414919","summary":null,"start":144525733,"end":144529132,"strand":-1,"description":"chromosome 8 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:33826]"}, {"versioned_ensembl_gene_id":"ENSG00000161642.17","gene_symbol":"ZNF385A","gene_name":"zinc finger protein 385A [Source:HGNC Symbol;Acc:HGNC:17521]","synonyms":"ZNF385,ZFP385,Hzf,DKFZp586G1122","biotype":"protein_coding","ncbi_id":"25946","summary":"Zinc finger proteins, such as ZNF385A, are regulatory proteins that act as transcription factors, bind single- or double-stranded RNA, or interact with other proteins (Sharma et al., 2004 [PubMed 15527981]).[supplied by OMIM, Oct 2008]","start":54369133,"end":54391298,"strand":-1,"description":"zinc finger protein 385A [Source:HGNC Symbol;Acc:HGNC:17521]"}, {"versioned_ensembl_gene_id":"ENSG00000143552.9","gene_symbol":"NUP210L","gene_name":"nucleoporin 210 like [Source:HGNC Symbol;Acc:HGNC:29915]","synonyms":null,"biotype":"protein_coding","ncbi_id":"91181","summary":null,"start":153992685,"end":154155116,"strand":-1,"description":"nucleoporin 210 like [Source:HGNC Symbol;Acc:HGNC:29915]"}, {"versioned_ensembl_gene_id":"ENSG00000260468.1","gene_symbol":"LINC01290","gene_name":"long intergenic non-protein coding RNA 1290 [Source:HGNC Symbol;Acc:HGNC:50356]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144584","summary":null,"start":10514842,"end":10528202,"strand":-1,"description":"long intergenic non-protein coding RNA 1290 [Source:HGNC Symbol;Acc:HGNC:50356]"}, {"versioned_ensembl_gene_id":"ENSG00000225824.8","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"IDDM1,HLA-DQB,CELIAC1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32811324,"end":32820618,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000236256.9","gene_symbol":"DIAPH2-AS1","gene_name":"DIAPH2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16972]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"10824","summary":null,"start":97431286,"end":97642589,"strand":-1,"description":"DIAPH2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16972]"}, {"versioned_ensembl_gene_id":"ENSG00000270961.1","gene_symbol":"IGHD5OR15-5A","gene_name":"immunoglobulin heavy diversity 5/OR15-5A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5512]","synonyms":"IGHD5OR155A,IGHD5/OR15-5A","biotype":"IG_D_gene","ncbi_id":"28327","summary":null,"start":20003840,"end":20003862,"strand":-1,"description":"immunoglobulin heavy diversity 5/OR15-5A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5512]"}, {"versioned_ensembl_gene_id":"ENSG00000241772.2","gene_symbol":"AC092620.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":138569090,"end":138574458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144228.8","gene_symbol":"SPOPL","gene_name":"speckle type BTB/POZ protein like [Source:HGNC Symbol;Acc:HGNC:27934]","synonyms":"BTBD33","biotype":"protein_coding","ncbi_id":"339745","summary":null,"start":138501801,"end":138573547,"strand":1,"description":"speckle type BTB/POZ protein like [Source:HGNC Symbol;Acc:HGNC:27934]"}, {"versioned_ensembl_gene_id":"ENSG00000254910.1","gene_symbol":"AC136475.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":310139,"end":311141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144290.16","gene_symbol":"SLC4A10","gene_name":"solute carrier family 4 member 10 [Source:HGNC Symbol;Acc:HGNC:13811]","synonyms":"NCBE,NBCn2","biotype":"protein_coding","ncbi_id":"57282","summary":"This gene belongs to a small family of sodium-coupled bicarbonate transporters (NCBTs) that regulate the intracellular pH of neurons, the secretion of bicarbonate ions across the choroid plexus, and the pH of the brain extracellular fluid. The protein encoded by this gene was initially identified as a sodium-driven chloride bicarbonate exchanger (NCBE) though there is now evidence that its sodium/bicarbonate cotransport activity is independent of any chloride ion countertransport under physiological conditions. This gene is now classified as a member A10 of the SLC4 family of transmembrane solute carriers. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]","start":161424332,"end":161985282,"strand":1,"description":"solute carrier family 4 member 10 [Source:HGNC Symbol;Acc:HGNC:13811]"}, {"versioned_ensembl_gene_id":"ENSG00000213440.2","gene_symbol":"H2AFZP1","gene_name":"H2A histone family member Z pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4742]","synonyms":"H2AFZP","biotype":"processed_pseudogene","ncbi_id":"54049","summary":null,"start":44046347,"end":44047041,"strand":-1,"description":"H2A histone family member Z pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4742]"}, {"versioned_ensembl_gene_id":"ENSG00000146963.17","gene_symbol":"LUC7L2","gene_name":"LUC7 like 2, pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:21608]","synonyms":"CGI-74,CGI-59,LUC7B2,H_NH0792N18.3,hLuc7B2,FLJ10657","biotype":"protein_coding","ncbi_id":"51631","summary":"This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":139340359,"end":139423457,"strand":1,"description":"LUC7 like 2, pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:21608]"}, {"versioned_ensembl_gene_id":"ENSG00000226053.1","gene_symbol":"LINC01776","gene_name":"long intergenic non-protein coding RNA 1776 [Source:HGNC Symbol;Acc:HGNC:52566]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729987","summary":null,"start":98210747,"end":98272658,"strand":1,"description":"long intergenic non-protein coding RNA 1776 [Source:HGNC Symbol;Acc:HGNC:52566]"}, {"versioned_ensembl_gene_id":"ENSG00000280040.1","gene_symbol":"AC095031.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":98660388,"end":98661059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233557.2","gene_symbol":"NFU1P2","gene_name":"NFU1 iron-sulfur cluster scaffold pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132699","summary":null,"start":98077000,"end":98077468,"strand":1,"description":"NFU1 iron-sulfur cluster scaffold pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44554]"}, {"versioned_ensembl_gene_id":"ENSG00000241490.1","gene_symbol":"AC093010.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":114214313,"end":114236204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240487.1","gene_symbol":"AC093010.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114231398,"end":114233021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248956.1","gene_symbol":"HMGB1P44","gene_name":"high mobility group box 1 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:39275]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130279","summary":null,"start":77963940,"end":77964511,"strand":1,"description":"high mobility group box 1 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:39275]"}, {"versioned_ensembl_gene_id":"ENSG00000092148.12","gene_symbol":"HECTD1","gene_name":"HECT domain E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:20157]","synonyms":"KIAA1131","biotype":"protein_coding","ncbi_id":"25831","summary":null,"start":31100112,"end":31207804,"strand":-1,"description":"HECT domain E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:20157]"}, {"versioned_ensembl_gene_id":"ENSG00000282150.1","gene_symbol":"AC234301.3","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106384472,"end":106384925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159398.15","gene_symbol":"CES5A","gene_name":"carboxylesterase 5A [Source:HGNC Symbol;Acc:HGNC:26459]","synonyms":"FLJ31547,CES7,CES5,CES4C1,CAUXIN","biotype":"protein_coding","ncbi_id":"221223","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They also participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene, also called CES5, is predominantly expressed in peripheral tissues, including brain, kidney, lung and testis. It encodes a secreted enzyme. Because of high levels in the urine of male domestic cats, this enzyme is also called cauxin (carboxylesterase-like urinary excreted protein). The enzyme functions in regulating the production of a pheromone precursor and may contribute to lipid and cholesterol transfer processes within male reproductive fluids. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":55846154,"end":55956031,"strand":-1,"description":"carboxylesterase 5A [Source:HGNC Symbol;Acc:HGNC:26459]"}, {"versioned_ensembl_gene_id":"ENSG00000213772.3","gene_symbol":"EIF1P7","gene_name":"eukaryotic translation initiation factor 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481691","summary":null,"start":9271292,"end":9271628,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49620]"}, {"versioned_ensembl_gene_id":"ENSG00000126267.8","gene_symbol":"COX6B1","gene_name":"cytochrome c oxidase subunit 6B1 [Source:HGNC Symbol;Acc:HGNC:2280]","synonyms":"COXG,COX6B","biotype":"protein_coding","ncbi_id":"1340","summary":"Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes subunit VIb. Mutations in this gene are associated with severe infantile encephalomyopathy. Three pseudogenes COX6BP-1, COX6BP-2 and COX6BP-3 have been found on chromosomes 7, 17 and 22q13.1-13.2, respectively. [provided by RefSeq, Jan 2010]","start":35648223,"end":35658861,"strand":1,"description":"cytochrome c oxidase subunit 6B1 [Source:HGNC Symbol;Acc:HGNC:2280]"}, {"versioned_ensembl_gene_id":"ENSG00000151577.12","gene_symbol":"DRD3","gene_name":"dopamine receptor D3 [Source:HGNC Symbol;Acc:HGNC:3024]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1814","summary":"This gene encodes the D3 subtype of the five (D1-D5) dopamine receptors. The activity of the D3 subtype receptor is mediated by G proteins which inhibit adenylyl cyclase. This receptor is localized to the limbic areas of the brain, which are associated with cognitive, emotional, and endocrine functions. Genetic variation in this gene may be associated with susceptibility to hereditary essential tremor 1. Alternative splicing of this gene results in transcript variants encoding different isoforms, although some variants may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Jul 2008]","start":114128652,"end":114199407,"strand":-1,"description":"dopamine receptor D3 [Source:HGNC Symbol;Acc:HGNC:3024]"}, {"versioned_ensembl_gene_id":"ENSG00000267088.1","gene_symbol":"AC087683.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42089312,"end":42089752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273165.1","gene_symbol":"AL121652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31852976,"end":31853423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271557.1","gene_symbol":"YPEL5P2","gene_name":"YPEL5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50556]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132562","summary":null,"start":47841324,"end":47841682,"strand":1,"description":"YPEL5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50556]"}, {"versioned_ensembl_gene_id":"ENSG00000237160.2","gene_symbol":"AC004022.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95348718,"end":95348910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275486.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816441,"end":54830746,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000179101.5","gene_symbol":"AL590139.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123514473,"end":123514872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188846.13","gene_symbol":"RPL14","gene_name":"ribosomal protein L14 [Source:HGNC Symbol;Acc:HGNC:10305]","synonyms":"RL14,L14,hRL14,CTG-B33","biotype":"protein_coding","ncbi_id":"9045","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L14E family of ribosomal proteins. It contains a basic region-leucine zipper (bZIP)-like domain. The protein is located in the cytoplasm. This gene contains a trinucleotide (GCT) repeat tract whose length is highly polymorphic; these triplet repeats result in a stretch of alanine residues in the encoded protein. Transcript variants utilizing alternative polyA signals and alternative 5'-terminal exons exist but all encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":40457292,"end":40468587,"strand":1,"description":"ribosomal protein L14 [Source:HGNC Symbol;Acc:HGNC:10305]"}, {"versioned_ensembl_gene_id":"ENSG00000188800.5","gene_symbol":"TMCO2","gene_name":"transmembrane and coiled-coil domains 2 [Source:HGNC Symbol;Acc:HGNC:23312]","synonyms":"dJ39G22.2","biotype":"protein_coding","ncbi_id":"127391","summary":null,"start":40245947,"end":40251691,"strand":1,"description":"transmembrane and coiled-coil domains 2 [Source:HGNC Symbol;Acc:HGNC:23312]"}, {"versioned_ensembl_gene_id":"ENSG00000228998.4","gene_symbol":"AC091167.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":90275129,"end":90275716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244510.2","gene_symbol":"AC008267.5","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66480394,"end":66490108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273275.1","gene_symbol":"AC017083.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68179833,"end":68180532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271537.1","gene_symbol":"AC009220.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139198557,"end":139199142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254592.1","gene_symbol":"AC123788.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3336721,"end":3340630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153246.12","gene_symbol":"PLA2R1","gene_name":"phospholipase A2 receptor 1 [Source:HGNC Symbol;Acc:HGNC:9042]","synonyms":"PLA2IR,PLA2G1R,PLA2-R,CLEC13C","biotype":"protein_coding","ncbi_id":"22925","summary":"This gene represents a phospholipase A2 receptor. The encoded protein likely exists as both a transmembrane form and a soluble form. The transmembrane receptor may play a role in clearance of phospholipase A2, thereby inhibiting its action. Polymorphisms at this locus have been associated with susceptibility to idiopathic membranous nephropathy. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]","start":159932006,"end":160062610,"strand":-1,"description":"phospholipase A2 receptor 1 [Source:HGNC Symbol;Acc:HGNC:9042]"}, {"versioned_ensembl_gene_id":"ENSG00000177476.3","gene_symbol":"OR2G3","gene_name":"olfactory receptor family 2 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:15008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81469","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247605586,"end":247606515,"strand":1,"description":"olfactory receptor family 2 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:15008]"}, {"versioned_ensembl_gene_id":"ENSG00000256083.1","gene_symbol":"AC090673.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65934777,"end":65948479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217801.9","gene_symbol":"AL390719.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1059734,"end":1069355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259905.5","gene_symbol":"PWRN1","gene_name":"Prader-Willi region non-protein coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:33235]","synonyms":"NCRNA00198","biotype":"lincRNA","ncbi_id":"791114","summary":"This gene is located in the Prader-Willi syndrome (PWS) region of chromosome 15, which is known to undergo imprinting. The transcript is believed to be non-coding. It is bi-allelically expressed in testis and kidney, but mono-allelically expressed from the paternal allele in brain. This gene is poly-adenylated and is known to undergo alternative splicing. Transcript variants may represent part of a complex imprinting center-SNURF-SNRPN transcription unit. The contribution of this gene to the PWS phenotype is unknown, but it has been suggested that it may play a role in establishing paternal imprinting in the PWS region, perhaps by maintaining the paternal allele in an open chromatin configuration. [provided by RefSeq, Sep 2009]","start":24493137,"end":24652130,"strand":1,"description":"Prader-Willi region non-protein coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:33235]"}, {"versioned_ensembl_gene_id":"ENSG00000240980.1","gene_symbol":"AC093904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9143166,"end":9146106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112761.20","gene_symbol":"WISP3","gene_name":"WNT1 inducible signaling pathway protein 3 [Source:HGNC Symbol;Acc:HGNC:12771]","synonyms":"CCN6","biotype":"protein_coding","ncbi_id":"8838","summary":"This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":112054072,"end":112070969,"strand":1,"description":"WNT1 inducible signaling pathway protein 3 [Source:HGNC Symbol;Acc:HGNC:12771]"}, {"versioned_ensembl_gene_id":"ENSG00000277710.1","gene_symbol":"AL589743.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19154134,"end":19155089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276177.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5.1,KIR2DL5,KIR2DL5,CD158F,KIR2DL5.1,CD158F","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54877583,"end":54887079,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000164096.12","gene_symbol":"C4orf3","gene_name":"chromosome 4 open reading frame 3 [Source:HGNC Symbol;Acc:HGNC:19225]","synonyms":"HCVFTP1","biotype":"protein_coding","ncbi_id":"401152","summary":null,"start":119296419,"end":119304445,"strand":-1,"description":"chromosome 4 open reading frame 3 [Source:HGNC Symbol;Acc:HGNC:19225]"}, {"versioned_ensembl_gene_id":"ENSG00000273761.5","gene_symbol":"DDX24","gene_name":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57062","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which shows little similarity to any of the other known human DEAD box proteins, but shows a high similarity to mouse Ddx24 at the amino acid level. [provided by RefSeq, Jul 2008]","start":94050920,"end":94081245,"strand":-1,"description":"DEAD-box helicase 24 [Source:HGNC Symbol;Acc:HGNC:13266]"}, {"versioned_ensembl_gene_id":"ENSG00000126804.13","gene_symbol":"ZBTB1","gene_name":"zinc finger and BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20259]","synonyms":"ZNF909,KIAA0997","biotype":"protein_coding","ncbi_id":"22890","summary":null,"start":64503712,"end":64533690,"strand":1,"description":"zinc finger and BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20259]"}, {"versioned_ensembl_gene_id":"ENSG00000206195.10","gene_symbol":"DUXAP8","gene_name":"double homeobox A pseudogene 8 [Source:NCBI gene;Acc:503637]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"503637","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":15784959,"end":15829984,"strand":1,"description":"double homeobox A pseudogene 8 [Source:NCBI gene;Acc:503637]"}, {"versioned_ensembl_gene_id":"ENSG00000105993.14","gene_symbol":"DNAJB6","gene_name":"DnaJ heat shock protein family (Hsp40) member B6 [Source:HGNC Symbol;Acc:HGNC:14888]","synonyms":"MRJ,LGMD1D","biotype":"protein_coding","ncbi_id":"10049","summary":"This gene encodes a member of the DNAJ protein family. DNAJ family members are characterized by a highly conserved amino acid stretch called the 'J-domain' and function as one of the two major classes of molecular chaperones involved in a wide range of cellular events, such as protein folding and oligomeric protein complex assembly. This family member may also play a role in polyglutamine aggregation in specific neurons. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":157335381,"end":157417439,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B6 [Source:HGNC Symbol;Acc:HGNC:14888]"}, {"versioned_ensembl_gene_id":"ENSG00000169203.16","gene_symbol":"NPIPB12","gene_name":"nuclear pore complex interacting protein family, member B12 [Source:HGNC Symbol;Acc:HGNC:37491]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440353","summary":null,"start":29483642,"end":29505999,"strand":-1,"description":"nuclear pore complex interacting protein family, member B12 [Source:HGNC Symbol;Acc:HGNC:37491]"}, {"versioned_ensembl_gene_id":"ENSG00000261221.3","gene_symbol":"ZNF865","gene_name":"zinc finger protein 865 [Source:HGNC Symbol;Acc:HGNC:38705]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507290","summary":null,"start":55605405,"end":55617269,"strand":1,"description":"zinc finger protein 865 [Source:HGNC Symbol;Acc:HGNC:38705]"}, {"versioned_ensembl_gene_id":"ENSG00000121940.15","gene_symbol":"CLCC1","gene_name":"chloride channel CLIC like 1 [Source:HGNC Symbol;Acc:HGNC:29675]","synonyms":"MCLC","biotype":"protein_coding","ncbi_id":"23155","summary":null,"start":108929508,"end":108963457,"strand":-1,"description":"chloride channel CLIC like 1 [Source:HGNC Symbol;Acc:HGNC:29675]"}, {"versioned_ensembl_gene_id":"ENSG00000196228.3","gene_symbol":"SULT1C3","gene_name":"sulfotransferase family 1C member 3 [Source:HGNC Symbol;Acc:HGNC:33543]","synonyms":null,"biotype":"protein_coding","ncbi_id":"442038","summary":null,"start":108247195,"end":108265351,"strand":1,"description":"sulfotransferase family 1C member 3 [Source:HGNC Symbol;Acc:HGNC:33543]"}, {"versioned_ensembl_gene_id":"ENSG00000260232.1","gene_symbol":"PWRN4","gene_name":"Prader-Willi region non-protein coding RNA 4 [Source:HGNC Symbol;Acc:HGNC:49130]","synonyms":"LINC01084","biotype":"lincRNA","ncbi_id":"104355151","summary":null,"start":23975172,"end":24003435,"strand":1,"description":"Prader-Willi region non-protein coding RNA 4 [Source:HGNC Symbol;Acc:HGNC:49130]"}, {"versioned_ensembl_gene_id":"ENSG00000136770.10","gene_symbol":"DNAJC1","gene_name":"DnaJ heat shock protein family (Hsp40) member C1 [Source:HGNC Symbol;Acc:HGNC:20090]","synonyms":"MTJ1,ERdj1,DNAJL1","biotype":"protein_coding","ncbi_id":"64215","summary":"The membrane protein encoded by this gene is a DNAJ-like heat shock protein that binds the molecular chaperone BiP. In addition, the encoded protein contains two SANT domains that have been shown to bind serpin alpha1-antichymotrypsin and inter-alpha trypsin inhibitor heavy chain 4. [provided by RefSeq, Jul 2016]","start":21756537,"end":22003769,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C1 [Source:HGNC Symbol;Acc:HGNC:20090]"}, {"versioned_ensembl_gene_id":"ENSG00000232099.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29671913,"end":29680622,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000236006.5","gene_symbol":"AL662848.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30788497,"end":30820509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234988.1","gene_symbol":"LINC01849","gene_name":"long intergenic non-protein coding RNA 1849 [Source:HGNC Symbol;Acc:HGNC:52665]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373507","summary":null,"start":100607028,"end":100609358,"strand":1,"description":"long intergenic non-protein coding RNA 1849 [Source:HGNC Symbol;Acc:HGNC:52665]"}, {"versioned_ensembl_gene_id":"ENSG00000226034.2","gene_symbol":"NANOGNBP1","gene_name":"NANOGNB pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42158]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100859926","summary":null,"start":100660199,"end":100660678,"strand":1,"description":"NANOGNB pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42158]"}, {"versioned_ensembl_gene_id":"ENSG00000274282.1","gene_symbol":"AC010133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19253960,"end":19260875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234497.5","gene_symbol":"ERICH3-AS1","gene_name":"ERICH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41093]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927320","summary":null,"start":74577430,"end":74626098,"strand":1,"description":"ERICH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41093]"}, {"versioned_ensembl_gene_id":"ENSG00000183856.10","gene_symbol":"IQGAP3","gene_name":"IQ motif containing GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:20669]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128239","summary":null,"start":156525405,"end":156572604,"strand":-1,"description":"IQ motif containing GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:20669]"}, {"versioned_ensembl_gene_id":"ENSG00000270076.1","gene_symbol":"AF131215.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11202965,"end":11203671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185275.6","gene_symbol":"CD24P4","gene_name":"CD24 molecule pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1649]","synonyms":"CD24L4","biotype":"processed_pseudogene","ncbi_id":"938","summary":null,"start":18992467,"end":18992709,"strand":-1,"description":"CD24 molecule pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1649]"}, {"versioned_ensembl_gene_id":"ENSG00000217896.2","gene_symbol":"ZNF839P1","gene_name":"zinc finger protein 839 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419733","summary":null,"start":18985175,"end":18986398,"strand":1,"description":"zinc finger protein 839 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38455]"}, {"versioned_ensembl_gene_id":"ENSG00000227809.1","gene_symbol":"AL355674.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74371531,"end":74383530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257653.1","gene_symbol":"AC117498.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48766194,"end":48767323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266306.1","gene_symbol":"AC061975.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28269203,"end":28272365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136628.17","gene_symbol":"EPRS","gene_name":"glutamyl-prolyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:3418]","synonyms":"QPRS,QARS,PARS,GLUPRORS,EARS","biotype":"protein_coding","ncbi_id":"2058","summary":"Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is a multifunctional aminoacyl-tRNA synthetase that catalyzes the aminoacylation of glutamic acid and proline tRNA species. Alternative splicing has been observed for this gene, but the full-length nature and biological validity of the variant have not been determined. [provided by RefSeq, Jul 2008]","start":219968601,"end":220046658,"strand":-1,"description":"glutamyl-prolyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:3418]"}, {"versioned_ensembl_gene_id":"ENSG00000281296.1","gene_symbol":"LL22NC03-63E9.3","gene_name":"uncharacterized LOC648691 [Source:NCBI gene;Acc:648691]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"648691","summary":null,"start":22568448,"end":22575707,"strand":1,"description":"uncharacterized LOC648691 [Source:NCBI gene;Acc:648691]"}, {"versioned_ensembl_gene_id":"ENSG00000235919.4","gene_symbol":"ASH1L-AS1","gene_name":"ASH1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44146]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"645676","summary":null,"start":155562042,"end":155563944,"strand":1,"description":"ASH1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44146]"}, {"versioned_ensembl_gene_id":"ENSG00000116539.12","gene_symbol":"ASH1L","gene_name":"ASH1 like histone lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:19088]","synonyms":"KMT2H,huASH1,ASH1L1,ASH1","biotype":"protein_coding","ncbi_id":"55870","summary":"This gene encodes a member of the trithorax group of transcriptional activators. The protein contains four AT hooks, a SET domain, a PHD-finger motif, and a bromodomain. It is localized to many small speckles in the nucleus, and also to cell-cell tight junctions. [provided by RefSeq, Jul 2008]","start":155335268,"end":155562807,"strand":-1,"description":"ASH1 like histone lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:19088]"}, {"versioned_ensembl_gene_id":"ENSG00000225350.1","gene_symbol":"FREM2-AS1","gene_name":"FREM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39964]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874073","summary":null,"start":38821798,"end":38827570,"strand":-1,"description":"FREM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39964]"}, {"versioned_ensembl_gene_id":"ENSG00000224236.3","gene_symbol":"MRRFP1","gene_name":"mitochondrial ribosome recycling factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35238]","synonyms":"MRRFP","biotype":"processed_pseudogene","ncbi_id":"286423","summary":null,"start":123116107,"end":123117781,"strand":-1,"description":"mitochondrial ribosome recycling factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35238]"}, {"versioned_ensembl_gene_id":"ENSG00000077713.18","gene_symbol":"SLC25A43","gene_name":"solute carrier family 25 member 43 [Source:HGNC Symbol;Acc:HGNC:30557]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203427","summary":"This gene encodes a member of the mitochondrial carrier family of proteins.[provided by RefSeq, Dec 2009]","start":119399060,"end":119454478,"strand":1,"description":"solute carrier family 25 member 43 [Source:HGNC Symbol;Acc:HGNC:30557]"}, {"versioned_ensembl_gene_id":"ENSG00000231782.6","gene_symbol":"LINC00575","gene_name":"long intergenic non-protein coding RNA 575 [Source:HGNC Symbol;Acc:HGNC:21342]","synonyms":"C4orf11","biotype":"lincRNA","ncbi_id":"439934","summary":null,"start":82613113,"end":82621437,"strand":-1,"description":"long intergenic non-protein coding RNA 575 [Source:HGNC Symbol;Acc:HGNC:21342]"}, {"versioned_ensembl_gene_id":"ENSG00000158125.9","gene_symbol":"XDH","gene_name":"xanthine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12805]","synonyms":"XOR,XO","biotype":"protein_coding","ncbi_id":"7498","summary":"Xanthine dehydrogenase belongs to the group of molybdenum-containing hydroxylases involved in the oxidative metabolism of purines. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Xanthine dehydrogenase can be converted to xanthine oxidase by reversible sulfhydryl oxidation or by irreversible proteolytic modification. Defects in xanthine dehydrogenase cause xanthinuria, may contribute to adult respiratory stress syndrome, and may potentiate influenza infection through an oxygen metabolite-dependent mechanism. [provided by RefSeq, Jan 2014]","start":31334321,"end":31414715,"strand":-1,"description":"xanthine dehydrogenase [Source:HGNC Symbol;Acc:HGNC:12805]"}, {"versioned_ensembl_gene_id":"ENSG00000232496.2","gene_symbol":"RPL3P12","gene_name":"ribosomal protein L3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131358","summary":null,"start":122538253,"end":122539460,"strand":1,"description":"ribosomal protein L3 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36298]"}, {"versioned_ensembl_gene_id":"ENSG00000280142.1","gene_symbol":"AL357562.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":122242008,"end":122242616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260585.1","gene_symbol":"AL359851.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121871869,"end":121876865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231965.4","gene_symbol":"AF131215.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11175051,"end":11175570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236216.5","gene_symbol":"PPP1R11P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"94297","summary":null,"start":21397987,"end":21398362,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16326]"}, {"versioned_ensembl_gene_id":"ENSG00000151093.7","gene_symbol":"OXSM","gene_name":"3-oxoacyl-ACP synthase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26063]","synonyms":"KS,FLJ20604,FASN2D,CEM1","biotype":"protein_coding","ncbi_id":"54995","summary":"This gene encodes a beta-ketoacyl synthetase. The encoded enzyme is required for elongation of fatty acid chains in the mitochondria. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2009]","start":25782917,"end":25794534,"strand":1,"description":"3-oxoacyl-ACP synthase, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26063]"}, {"versioned_ensembl_gene_id":"ENSG00000166527.7","gene_symbol":"CLEC4D","gene_name":"C-type lectin domain family 4 member D [Source:HGNC Symbol;Acc:HGNC:14554]","synonyms":"Mpcl,CLECSF8,CD368","biotype":"protein_coding","ncbi_id":"338339","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":8509475,"end":8522366,"strand":1,"description":"C-type lectin domain family 4 member D [Source:HGNC Symbol;Acc:HGNC:14554]"}, {"versioned_ensembl_gene_id":"ENSG00000206432.4","gene_symbol":"TMEM200C","gene_name":"transmembrane protein 200C [Source:HGNC Symbol;Acc:HGNC:37208]","synonyms":"TTMA","biotype":"protein_coding","ncbi_id":"645369","summary":null,"start":5882072,"end":5895955,"strand":-1,"description":"transmembrane protein 200C [Source:HGNC Symbol;Acc:HGNC:37208]"}, {"versioned_ensembl_gene_id":"ENSG00000114698.14","gene_symbol":"PLSCR4","gene_name":"phospholipid scramblase 4 [Source:HGNC Symbol;Acc:HGNC:16497]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57088","summary":null,"start":146192339,"end":146251179,"strand":-1,"description":"phospholipid scramblase 4 [Source:HGNC Symbol;Acc:HGNC:16497]"}, {"versioned_ensembl_gene_id":"ENSG00000242247.10","gene_symbol":"ARFGAP3","gene_name":"ADP ribosylation factor GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:661]","synonyms":"ARFGAP1","biotype":"protein_coding","ncbi_id":"26286","summary":"The protein encoded by this gene is a GTPase-activating protein (GAP) that associates with the Golgi apparatus and regulates the early secretory pathway of proteins. The encoded protein promotes hydrolysis of ADP-ribosylation factor 1 (ARF1)-bound GTP, which is required for the dissociation of coat proteins from Golgi-derived membranes and vesicles. Dissociation of the coat proteins is a prerequisite for the fusion of these vesicles with target compartments. The activity of this protein is sensitive to phospholipids. Multiple transcript variants encoding different isoforms have been found for this gene. This gene was originally known as ARFGAP1, but that is now the name of a related but different gene. [provided by RefSeq, Nov 2008]","start":42796502,"end":42858106,"strand":-1,"description":"ADP ribosylation factor GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:661]"}, {"versioned_ensembl_gene_id":"ENSG00000187527.10","gene_symbol":"ATP13A5","gene_name":"ATPase 13A5 [Source:HGNC Symbol;Acc:HGNC:31789]","synonyms":"FLJ16025","biotype":"protein_coding","ncbi_id":"344905","summary":"This gene encodes a member of the P5 subfamily of P-type transport ATPases. P-type ATPases form a large superfamily of cation and lipid pumps that transport inorganic cations and other substrates across cell membranes. P5 ATPases are localized to membranes of the endoplasmic reticulum (ER) and serve many important functions including transport of cargo proteins to the Golgi, glycosylation and cell wall biosynthesis, control of protein insertion orientation, 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) degradation, and sensitivity to unfolded protein response (UPR) activators. The encoded protein is organized into three cytoplasmic domains (A, P, and N) and two membrane-embedded domains (T and S). The N-domain binds ATP and serves as a built-in protein kinase, which phosphorylates the P-domain. The A-domain is an intrinsic protein phosphatase, which dephosphorylates the P-domain once during each catalytic cycle. [provided by RefSeq, Jul 2017]","start":193274790,"end":193378843,"strand":-1,"description":"ATPase 13A5 [Source:HGNC Symbol;Acc:HGNC:31789]"}, {"versioned_ensembl_gene_id":"ENSG00000273562.4","gene_symbol":"NAP1L4","gene_name":"nucleosome assembly protein 1 like 4 [Source:HGNC Symbol;Acc:HGNC:7640]","synonyms":"NAP2","biotype":"protein_coding","ncbi_id":"4676","summary":"This gene encodes a member of the nucleosome assembly protein (NAP) family which can interact with both core and linker histones. It can shuttle between the cytoplasm and nucleus, suggesting a role as a histone chaperone. This gene is one of several located near the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. [provided by RefSeq, Jul 2008]","start":2943292,"end":2991260,"strand":-1,"description":"nucleosome assembly protein 1 like 4 [Source:HGNC Symbol;Acc:HGNC:7640]"}, {"versioned_ensembl_gene_id":"ENSG00000254132.1","gene_symbol":"MTND6P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39466]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478942","summary":null,"start":94568929,"end":94569470,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39466]"}, {"versioned_ensembl_gene_id":"ENSG00000100033.16","gene_symbol":"PRODH","gene_name":"proline dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:9453]","synonyms":"PRODH2,PRODH1,PIG6,HSPOX2,TP53I6","biotype":"protein_coding","ncbi_id":"5625","summary":"This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]","start":18912777,"end":18936553,"strand":-1,"description":"proline dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:9453]"}, {"versioned_ensembl_gene_id":"ENSG00000180974.4","gene_symbol":"OR52E4","gene_name":"olfactory receptor family 52 subfamily E member 4 [Source:HGNC Symbol;Acc:HGNC:15213]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390081","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5880629,"end":5887079,"strand":1,"description":"olfactory receptor family 52 subfamily E member 4 [Source:HGNC Symbol;Acc:HGNC:15213]"}, {"versioned_ensembl_gene_id":"ENSG00000278377.1","gene_symbol":"OR2T3","gene_name":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343173","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248479392,"end":248480399,"strand":1,"description":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]"}, {"versioned_ensembl_gene_id":"ENSG00000179965.11","gene_symbol":"ZNF771","gene_name":"zinc finger protein 771 [Source:HGNC Symbol;Acc:HGNC:29653]","synonyms":"DSC43","biotype":"protein_coding","ncbi_id":"51333","summary":null,"start":30407297,"end":30431108,"strand":1,"description":"zinc finger protein 771 [Source:HGNC Symbol;Acc:HGNC:29653]"}, {"versioned_ensembl_gene_id":"ENSG00000280552.1","gene_symbol":"AC107622.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20347019,"end":20355479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229532.1","gene_symbol":"AC105443.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132086266,"end":132087992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276821.1","gene_symbol":"OR2T2","gene_name":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]","synonyms":"OR2T2P","biotype":"protein_coding","ncbi_id":"401992","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248458842,"end":248459895,"strand":1,"description":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]"}, {"versioned_ensembl_gene_id":"ENSG00000234766.1","gene_symbol":"LINC01496","gene_name":"long intergenic non-protein coding RNA 1496 [Source:HGNC Symbol;Acc:HGNC:51162]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723426","summary":null,"start":51502090,"end":51511005,"strand":-1,"description":"long intergenic non-protein coding RNA 1496 [Source:HGNC Symbol;Acc:HGNC:51162]"}, {"versioned_ensembl_gene_id":"ENSG00000140993.10","gene_symbol":"TIGD7","gene_name":"tigger transposable element derived 7 [Source:HGNC Symbol;Acc:HGNC:18331]","synonyms":"Sancho","biotype":"protein_coding","ncbi_id":"91151","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":3298832,"end":3305729,"strand":-1,"description":"tigger transposable element derived 7 [Source:HGNC Symbol;Acc:HGNC:18331]"}, {"versioned_ensembl_gene_id":"ENSG00000135624.15","gene_symbol":"CCT7","gene_name":"chaperonin containing TCP1 subunit 7 [Source:HGNC Symbol;Acc:HGNC:1622]","synonyms":"Nip7-1,Ccth","biotype":"protein_coding","ncbi_id":"10574","summary":"This gene encodes a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 5 and 6. [provided by RefSeq, Oct 2009]","start":73233420,"end":73253021,"strand":1,"description":"chaperonin containing TCP1 subunit 7 [Source:HGNC Symbol;Acc:HGNC:1622]"}, {"versioned_ensembl_gene_id":"ENSG00000148459.15","gene_symbol":"PDSS1","gene_name":"decaprenyl diphosphate synthase subunit 1 [Source:HGNC Symbol;Acc:HGNC:17759]","synonyms":"TPT,TPRT,COQ1","biotype":"protein_coding","ncbi_id":"23590","summary":"The protein encoded by this gene is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in this gene are a cause of coenzyme Q10 deficiency. [provided by RefSeq, Jul 2008]","start":26697659,"end":26746798,"strand":1,"description":"decaprenyl diphosphate synthase subunit 1 [Source:HGNC Symbol;Acc:HGNC:17759]"}, {"versioned_ensembl_gene_id":"ENSG00000234832.1","gene_symbol":"AL096677.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23346941,"end":23351486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182890.4","gene_symbol":"GLUD2","gene_name":"glutamate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:4336]","synonyms":"GLUDP1","biotype":"protein_coding","ncbi_id":"2747","summary":"The protein encoded by this gene is localized to the mitochondrion and acts as a homohexamer to recycle glutamate during neurotransmission. The encoded enzyme catalyzes the reversible oxidative deamination of glutamate to alpha-ketoglutarate. This gene is intronless.[provided by RefSeq, Jan 2010]","start":121047588,"end":121050080,"strand":1,"description":"glutamate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:4336]"}, {"versioned_ensembl_gene_id":"ENSG00000274229.2","gene_symbol":"SOCS7","gene_name":"suppressor of cytokine signaling 7 [Source:HGNC Symbol;Acc:HGNC:29846]","synonyms":"NCKAP4,NAP4","biotype":"protein_coding","ncbi_id":"30837","summary":null,"start":38152644,"end":38206380,"strand":1,"description":"suppressor of cytokine signaling 7 [Source:HGNC Symbol;Acc:HGNC:29846]"}, {"versioned_ensembl_gene_id":"ENSG00000224683.1","gene_symbol":"RPL36AP29","gene_name":"ribosomal protein L36a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36897]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271510","summary":null,"start":16208945,"end":16209265,"strand":1,"description":"ribosomal protein L36a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36897]"}, {"versioned_ensembl_gene_id":"ENSG00000236189.2","gene_symbol":"RPL18AP15","gene_name":"ribosomal protein L18a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36010]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392522","summary":null,"start":111624210,"end":111624726,"strand":-1,"description":"ribosomal protein L18a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36010]"}, {"versioned_ensembl_gene_id":"ENSG00000204918.3","gene_symbol":"PRR20B","gene_name":"proline rich 20B [Source:HGNC Symbol;Acc:HGNC:37220]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729233","summary":"This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008]","start":57147488,"end":57150509,"strand":1,"description":"proline rich 20B [Source:HGNC Symbol;Acc:HGNC:37220]"}, {"versioned_ensembl_gene_id":"ENSG00000182873.5","gene_symbol":"PRKCZ-AS1","gene_name":"PRKCZ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40477]","synonyms":"RP11-181G12.2","biotype":"antisense_RNA","ncbi_id":"100506504","summary":null,"start":2181794,"end":2184389,"strand":-1,"description":"PRKCZ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40477]"}, {"versioned_ensembl_gene_id":"ENSG00000144331.18","gene_symbol":"ZNF385B","gene_name":"zinc finger protein 385B [Source:HGNC Symbol;Acc:HGNC:26332]","synonyms":"ZNF533,FLJ25270","biotype":"protein_coding","ncbi_id":"151126","summary":null,"start":179441982,"end":179861505,"strand":-1,"description":"zinc finger protein 385B [Source:HGNC Symbol;Acc:HGNC:26332]"}, {"versioned_ensembl_gene_id":"ENSG00000160799.11","gene_symbol":"CCDC12","gene_name":"coiled-coil domain containing 12 [Source:HGNC Symbol;Acc:HGNC:28332]","synonyms":"MGC23918","biotype":"protein_coding","ncbi_id":"151903","summary":null,"start":46921726,"end":46982010,"strand":-1,"description":"coiled-coil domain containing 12 [Source:HGNC Symbol;Acc:HGNC:28332]"}, {"versioned_ensembl_gene_id":"ENSG00000279581.1","gene_symbol":"AC073862.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130980667,"end":130981367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249947.2","gene_symbol":"XBP1P1","gene_name":"X-box binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12802]","synonyms":"XBPP1,XBP1","biotype":"processed_pseudogene","ncbi_id":"7495","summary":null,"start":112885094,"end":112885745,"strand":1,"description":"X-box binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12802]"}, {"versioned_ensembl_gene_id":"ENSG00000282653.1","gene_symbol":"IGHV3-16","gene_name":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28447","summary":null,"start":106165976,"end":106166501,"strand":-1,"description":"immunoglobulin heavy variable 3-16 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5583]"}, {"versioned_ensembl_gene_id":"ENSG00000250045.2","gene_symbol":"CBX3P3","gene_name":"chromobox 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42875]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421861","summary":null,"start":112777630,"end":112778161,"strand":-1,"description":"chromobox 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42875]"}, {"versioned_ensembl_gene_id":"ENSG00000077458.12","gene_symbol":"FAM76B","gene_name":"family with sequence similarity 76 member B [Source:HGNC Symbol;Acc:HGNC:28492]","synonyms":"MGC33371","biotype":"protein_coding","ncbi_id":"143684","summary":null,"start":95768942,"end":95790409,"strand":-1,"description":"family with sequence similarity 76 member B [Source:HGNC Symbol;Acc:HGNC:28492]"}, {"versioned_ensembl_gene_id":"ENSG00000161103.11","gene_symbol":"AC008132.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18846811,"end":18861049,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215544.6","gene_symbol":"BCRP7","gene_name":"breakpoint cluster region pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39075]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100133163","summary":null,"start":18855621,"end":18858640,"strand":-1,"description":"breakpoint cluster region pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39075]"}, {"versioned_ensembl_gene_id":"ENSG00000213280.2","gene_symbol":"AC090114.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128570241,"end":128570688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187546.13","gene_symbol":"AGMO","gene_name":"alkylglycerol monooxygenase [Source:HGNC Symbol;Acc:HGNC:33784]","synonyms":"TMEM195,FLJ16237","biotype":"protein_coding","ncbi_id":"392636","summary":"The protein encoded by this gene is a tetrahydrobiopterin- and iron-dependent enzyme that cleaves the ether bond of alkylglycerols. Sequence comparisons distinguish this protein as forming a third, distinct class of tetrahydrobiopterin-dependent enzymes. Variations in this gene have been associated with decreased glucose-stimulated insulin response, type 2 diabetes, and susceptibility to intracranial aneurysms. [provided by RefSeq, Aug 2012]","start":15200318,"end":15562015,"strand":-1,"description":"alkylglycerol monooxygenase [Source:HGNC Symbol;Acc:HGNC:33784]"}, {"versioned_ensembl_gene_id":"ENSG00000228806.1","gene_symbol":"AC092628.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155106400,"end":155106651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219607.3","gene_symbol":"PPP1R3G","gene_name":"protein phosphatase 1 regulatory subunit 3G [Source:HGNC Symbol;Acc:HGNC:14945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"648791","summary":null,"start":5084581,"end":5089487,"strand":1,"description":"protein phosphatase 1 regulatory subunit 3G [Source:HGNC Symbol;Acc:HGNC:14945]"}, {"versioned_ensembl_gene_id":"ENSG00000136149.6","gene_symbol":"RPL13AP25","gene_name":"ribosomal protein L13a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36981]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287887","summary":null,"start":54440704,"end":54441315,"strand":-1,"description":"ribosomal protein L13a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36981]"}, {"versioned_ensembl_gene_id":"ENSG00000121377.2","gene_symbol":"TAS2R7","gene_name":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]","synonyms":"TRB4,T2R7","biotype":"protein_coding","ncbi_id":"50837","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10801532,"end":10802627,"strand":-1,"description":"taste 2 receptor member 7 [Source:HGNC Symbol;Acc:HGNC:14913]"}, {"versioned_ensembl_gene_id":"ENSG00000182330.10","gene_symbol":"PRAMEF8","gene_name":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391002","summary":null,"start":13281035,"end":13285174,"strand":-1,"description":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]"}, {"versioned_ensembl_gene_id":"ENSG00000179300.3","gene_symbol":"RTL3","gene_name":"retrotransposon Gag like 3 [Source:HGNC Symbol;Acc:HGNC:22997]","synonyms":"ZHC5,ZCCHC5,SIRH9,Mart3,Mar3,FLJ38865","biotype":"protein_coding","ncbi_id":"203430","summary":"This gene is a member of a family of gag-related retrotransposon genes. These genes appear to have lost the ability to retrotranspose; however, their open reading frames have remained intact, which may indicate that these genes have acquired new functions in the cell. [provided by RefSeq, Nov 2009]","start":78656069,"end":78659328,"strand":-1,"description":"retrotransposon Gag like 3 [Source:HGNC Symbol;Acc:HGNC:22997]"}, {"versioned_ensembl_gene_id":"ENSG00000235390.4","gene_symbol":"AC051619.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45321077,"end":45321692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230285.1","gene_symbol":"AC092807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85599131,"end":85600734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177692.11","gene_symbol":"DNAJC28","gene_name":"DnaJ heat shock protein family (Hsp40) member C28 [Source:HGNC Symbol;Acc:HGNC:1297]","synonyms":"C21orf78,C21orf55","biotype":"protein_coding","ncbi_id":"54943","summary":"This gene encodes a member of the DnaJ heat shock protein family. The encoded protein, which contains a conserved N-terminal DnaJ domain, is thought to play a role in protein folding or act as a molecular chaperone protein. [provided by RefSeq, Oct 2016]","start":33485530,"end":33491720,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C28 [Source:HGNC Symbol;Acc:HGNC:1297]"}, {"versioned_ensembl_gene_id":"ENSG00000170092.14","gene_symbol":"SPDYE5","gene_name":"speedy/RINGO cell cycle regulator family member E5 [Source:HGNC Symbol;Acc:HGNC:35464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"442590","summary":null,"start":75493625,"end":75504304,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E5 [Source:HGNC Symbol;Acc:HGNC:35464]"}, {"versioned_ensembl_gene_id":"ENSG00000243584.1","gene_symbol":"AC068769.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183613620,"end":183616742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236902.8","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"G6D,MEGT1,C6orf23,Ly6-D,NG25","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31783184,"end":31794200,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000232392.1","gene_symbol":"AC002366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11334233,"end":11335901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172531.14","gene_symbol":"PPP1CA","gene_name":"protein phosphatase 1 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9281]","synonyms":"PPP1A,PP1alpha,PP1A,PP-1A","biotype":"protein_coding","ncbi_id":"5499","summary":"The protein encoded by this gene is one of the three catalytic subunits of protein phosphatase 1 (PP1). This broadly expressed gene encodes the alpha subunit of the PP1 complex that associates with over 200 regulatory proteins to form holoenzymes which dephosphorylate their biological targets with high specificity. PP1 is a serine/threonine specific protein phosphatase known to be involved in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription. Increased PP1 activity has been observed in the end stage of heart failure. Studies suggest that PP1 is an important regulator of cardiac function and that PP1 deregulation is implicated in diabetes and multiple types of cancer. Three alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2020]","start":67398183,"end":67421183,"strand":-1,"description":"protein phosphatase 1 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9281]"}, {"versioned_ensembl_gene_id":"ENSG00000156471.12","gene_symbol":"PTDSS1","gene_name":"phosphatidylserine synthase 1 [Source:HGNC Symbol;Acc:HGNC:9587]","synonyms":"PSSA,KIAA0024,PSS1","biotype":"protein_coding","ncbi_id":"9791","summary":"The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]","start":96261715,"end":96336995,"strand":1,"description":"phosphatidylserine synthase 1 [Source:HGNC Symbol;Acc:HGNC:9587]"}, {"versioned_ensembl_gene_id":"ENSG00000273505.1","gene_symbol":"TAS2R42","gene_name":"taste 2 receptor member 42 [Source:HGNC Symbol;Acc:HGNC:18888]","synonyms":"TAS2R55,T2R55,T2R24,hT2R55","biotype":"protein_coding","ncbi_id":"353164","summary":null,"start":11182250,"end":11183194,"strand":-1,"description":"taste 2 receptor member 42 [Source:HGNC Symbol;Acc:HGNC:18888]"}, {"versioned_ensembl_gene_id":"ENSG00000136267.13","gene_symbol":"DGKB","gene_name":"diacylglycerol kinase beta [Source:HGNC Symbol;Acc:HGNC:2850]","synonyms":"KIAA0718,DGK-BETA,DGK,DAGK2","biotype":"protein_coding","ncbi_id":"1607","summary":"Diacylglycerol kinases (DGKs) are regulators of the intracellular concentration of the second messenger diacylglycerol (DAG) and thus play a key role in cellular processes. Nine mammalian isotypes have been identified, which are encoded by separate genes. Mammalian DGK isozymes contain a conserved catalytic (kinase) domain and a cysteine-rich domain (CRD). The protein encoded by this gene is a diacylglycerol kinase, beta isotype. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2017]","start":14145049,"end":14974777,"strand":-1,"description":"diacylglycerol kinase beta [Source:HGNC Symbol;Acc:HGNC:2850]"}, {"versioned_ensembl_gene_id":"ENSG00000180035.12","gene_symbol":"ZNF48","gene_name":"zinc finger protein 48 [Source:HGNC Symbol;Acc:HGNC:13114]","synonyms":"MGC43952,FLJ31751,DKFZp762K013,ZNF553","biotype":"protein_coding","ncbi_id":"197407","summary":null,"start":30378106,"end":30400108,"strand":1,"description":"zinc finger protein 48 [Source:HGNC Symbol;Acc:HGNC:13114]"}, {"versioned_ensembl_gene_id":"ENSG00000284649.1","gene_symbol":"AC009093.8","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29113050,"end":29217860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233980.1","gene_symbol":"FDPSP2","gene_name":"farnesyl diphosphate synthase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3633]","synonyms":"TCAG_1641456,FPSL2,FDPSL2A,FDPSL2","biotype":"processed_pseudogene","ncbi_id":"619190","summary":null,"start":76470162,"end":76471058,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3633]"}, {"versioned_ensembl_gene_id":"ENSG00000273141.1","gene_symbol":"AP001269.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11908712,"end":11909223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283932.1","gene_symbol":"AL121722.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22560553,"end":22584261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167531.6","gene_symbol":"LALBA","gene_name":"lactalbumin alpha [Source:HGNC Symbol;Acc:HGNC:6480]","synonyms":"LYZL7","biotype":"protein_coding","ncbi_id":"3906","summary":"This gene encodes alpha-lactalbumin, a principal protein of milk. Alpha-lactalbumin forms the regulatory subunit of the lactose synthase (LS) heterodimer and beta 1,4-galactosyltransferase (beta4Gal-T1) forms the catalytic component. Together, these proteins enable LS to produce lactose by transfering galactose moieties to glucose. As a monomer, alpha-lactalbumin strongly binds calcium and zinc ions and may possess bactericidal or antitumor activity. A folding variant of alpha-lactalbumin, called HAMLET, likely induces apoptosis in tumor and immature cells. [provided by RefSeq, Jul 2008]","start":48567684,"end":48570066,"strand":-1,"description":"lactalbumin alpha [Source:HGNC Symbol;Acc:HGNC:6480]"}, {"versioned_ensembl_gene_id":"ENSG00000229571.7","gene_symbol":"PRAMEF25","gene_name":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441873","summary":null,"start":13068677,"end":13077884,"strand":1,"description":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]"}, {"versioned_ensembl_gene_id":"ENSG00000008282.8","gene_symbol":"SYPL1","gene_name":"synaptophysin like 1 [Source:HGNC Symbol;Acc:HGNC:11507]","synonyms":"SYPL","biotype":"protein_coding","ncbi_id":"6856","summary":null,"start":106090503,"end":106112576,"strand":-1,"description":"synaptophysin like 1 [Source:HGNC Symbol;Acc:HGNC:11507]"}, {"versioned_ensembl_gene_id":"ENSG00000284699.1","gene_symbol":"AL445648.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24704894,"end":24717596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267961.1","gene_symbol":"OR10B1P","gene_name":"olfactory receptor family 10 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8163]","synonyms":"OR10B2","biotype":"unprocessed_pseudogene","ncbi_id":"401903","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15141132,"end":15142038,"strand":-1,"description":"olfactory receptor family 10 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8163]"}, {"versioned_ensembl_gene_id":"ENSG00000243018.1","gene_symbol":"AC005486.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151249325,"end":151254390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082014.16","gene_symbol":"SMARCD3","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 [Source:HGNC Symbol;Acc:HGNC:11108]","synonyms":"Rsc6p,CRACD3,BAF60C","biotype":"protein_coding","ncbi_id":"6604","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":151238764,"end":151277896,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 [Source:HGNC Symbol;Acc:HGNC:11108]"}, {"versioned_ensembl_gene_id":"ENSG00000242950.6","gene_symbol":"ERVW-1","gene_name":"endogenous retrovirus group W member 1, envelope [Source:HGNC Symbol;Acc:HGNC:13525]","synonyms":"HERVW,HERV-W-ENV,HERV-W,HERV-7q,ERVWE1,envW","biotype":"protein_coding","ncbi_id":"30816","summary":"Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on chromosome 7 that has inactivating mutations in the gag and pol genes. This gene is the envelope glycoprotein gene which appears to have been selectively preserved. The gene's protein product is expressed in the placental syncytiotrophoblast and is involved in fusion of the cytotrophoblast cells to form the syncytial layer of the placenta. The protein has the characteristics of a typical retroviral envelope protein, including a furin cleavage site that separates the surface (SU) and transmembrane (TM) proteins which form a heterodimer. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Mar 2010]","start":92468380,"end":92477986,"strand":-1,"description":"endogenous retrovirus group W member 1, envelope [Source:HGNC Symbol;Acc:HGNC:13525]"}, {"versioned_ensembl_gene_id":"ENSG00000104897.9","gene_symbol":"SF3A2","gene_name":"splicing factor 3a subunit 2 [Source:HGNC Symbol;Acc:HGNC:10766]","synonyms":"SF3a66,SAP62,PRPF11,Prp11","biotype":"protein_coding","ncbi_id":"8175","summary":"This gene encodes subunit 2 of the splicing factor 3a protein complex. The splicing factor 3a heterotrimer includes subunits 1, 2 and 3 and is necessary for the in vitro conversion of 15S U2 snRNP into an active 17S particle that performs pre-mRNA splicing. Subunit 2 interacts with subunit 1 through its amino-terminus while the single zinc finger domain of subunit 2 plays a role in its binding to the 15S U2 snRNP. Subunit 2 may also function independently of its RNA splicing function as a microtubule-binding protein. [provided by RefSeq, Jul 2008]","start":2236504,"end":2248679,"strand":1,"description":"splicing factor 3a subunit 2 [Source:HGNC Symbol;Acc:HGNC:10766]"}, {"versioned_ensembl_gene_id":"ENSG00000223653.5","gene_symbol":"AL078459.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85276715,"end":85448124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213729.3","gene_symbol":"AC098828.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20155618,"end":20156057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223734.2","gene_symbol":"AC098828.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20052134,"end":20054496,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215313.3","gene_symbol":"RPL6P30","gene_name":"ribosomal protein L6 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36171]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139452","summary":null,"start":16198428,"end":16199289,"strand":-1,"description":"ribosomal protein L6 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36171]"}, {"versioned_ensembl_gene_id":"ENSG00000225406.1","gene_symbol":"AC080125.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185547135,"end":185547818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236334.2","gene_symbol":"PPIAL4G","gene_name":"peptidylprolyl isomerase A like 4G [Source:HGNC Symbol;Acc:HGNC:33996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644591","summary":null,"start":148479824,"end":148483679,"strand":-1,"description":"peptidylprolyl isomerase A like 4G [Source:HGNC Symbol;Acc:HGNC:33996]"}, {"versioned_ensembl_gene_id":"ENSG00000228219.1","gene_symbol":"NPM1P30","gene_name":"nucleophosmin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45209]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101928904","summary":null,"start":21110682,"end":21113388,"strand":1,"description":"nucleophosmin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:45209]"}, {"versioned_ensembl_gene_id":"ENSG00000231920.1","gene_symbol":"NEBL-AS1","gene_name":"NEBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44899]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128511","summary":null,"start":21174014,"end":21175048,"strand":1,"description":"NEBL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44899]"}, {"versioned_ensembl_gene_id":"ENSG00000267882.2","gene_symbol":"AL031666.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47318502,"end":47320754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135373.12","gene_symbol":"EHF","gene_name":"ETS homologous factor [Source:HGNC Symbol;Acc:HGNC:3246]","synonyms":"ESEJ,ESE3","biotype":"protein_coding","ncbi_id":"26298","summary":"This gene encodes a protein that belongs to an ETS transcription factor subfamily characterized by epithelial-specific expression (ESEs). The encoded protein acts as a transcriptional repressor and may be involved in epithelial differentiation and carcinogenesis. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":34621093,"end":34661057,"strand":1,"description":"ETS homologous factor [Source:HGNC Symbol;Acc:HGNC:3246]"}, {"versioned_ensembl_gene_id":"ENSG00000187824.8","gene_symbol":"TMEM220","gene_name":"transmembrane protein 220 [Source:HGNC Symbol;Acc:HGNC:33757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388335","summary":null,"start":10699015,"end":10730316,"strand":-1,"description":"transmembrane protein 220 [Source:HGNC Symbol;Acc:HGNC:33757]"}, {"versioned_ensembl_gene_id":"ENSG00000278310.2","gene_symbol":"GOLGA8F","gene_name":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]","synonyms":"DKFZp434P162","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132565","summary":null,"start":28491516,"end":28504915,"strand":1,"description":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]"}, {"versioned_ensembl_gene_id":"ENSG00000160209.18","gene_symbol":"PDXK","gene_name":"pyridoxal kinase [Source:HGNC Symbol;Acc:HGNC:8819]","synonyms":"PRED79,PNK,PKH,MGC15873,FLJ31940,FLJ21324,C21orf97,C21orf124","biotype":"protein_coding","ncbi_id":"8566","summary":"The protein encoded by this gene phosphorylates vitamin B6, a step required for the conversion of vitamin B6 to pyridoxal-5-phosphate, an important cofactor in intermediary metabolism. The encoded protein is cytoplasmic and probably acts as a homodimer. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":43719094,"end":43762307,"strand":1,"description":"pyridoxal kinase [Source:HGNC Symbol;Acc:HGNC:8819]"}, {"versioned_ensembl_gene_id":"ENSG00000054598.6","gene_symbol":"FOXC1","gene_name":"forkhead box C1 [Source:HGNC Symbol;Acc:HGNC:3800]","synonyms":"IRID1,IHG1,IGDA,FREAC3,FKHL7,ARA","biotype":"protein_coding","ncbi_id":"2296","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly. [provided by RefSeq, Jul 2008]","start":1609972,"end":1613897,"strand":1,"description":"forkhead box C1 [Source:HGNC Symbol;Acc:HGNC:3800]"}, {"versioned_ensembl_gene_id":"ENSG00000240902.1","gene_symbol":"APOOP2","gene_name":"apolipoprotein O pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129005","summary":null,"start":87594838,"end":87595376,"strand":1,"description":"apolipoprotein O pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48740]"}, {"versioned_ensembl_gene_id":"ENSG00000132031.12","gene_symbol":"MATN3","gene_name":"matrilin 3 [Source:HGNC Symbol;Acc:HGNC:6909]","synonyms":"HOA,EDM5","biotype":"protein_coding","ncbi_id":"4148","summary":"This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains two von Willebrand factor A domains; it is present in the cartilage extracellular matrix and has a role in the development and homeostasis of cartilage and bone. Mutations in this gene result in multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008]","start":19992111,"end":20012694,"strand":-1,"description":"matrilin 3 [Source:HGNC Symbol;Acc:HGNC:6909]"}, {"versioned_ensembl_gene_id":"ENSG00000271911.1","gene_symbol":"AL357054.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":761675,"end":780648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270084.1","gene_symbol":"GAS5-AS1","gene_name":"GAS5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44119]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506046","summary":null,"start":173863248,"end":173863941,"strand":1,"description":"GAS5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44119]"}, {"versioned_ensembl_gene_id":"ENSG00000226406.1","gene_symbol":"RBMX2P1","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128341","summary":null,"start":14829154,"end":14829989,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39923]"}, {"versioned_ensembl_gene_id":"ENSG00000133107.14","gene_symbol":"TRPC4","gene_name":"transient receptor potential cation channel subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:12336]","synonyms":"HTRP4,TRP4","biotype":"protein_coding","ncbi_id":"7223","summary":"This gene encodes a member of the canonical subfamily of transient receptor potential cation channels. The encoded protein forms a non-selective calcium-permeable cation channel that is activated by Gq-coupled receptors and tyrosine kinases, and plays a role in multiple processes including endothelial permeability, vasodilation, neurotransmitter release and cell proliferation. Single nucleotide polymorphisms in this gene may be associated with generalized epilepsy with photosensitivity. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":37636636,"end":37870425,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:12336]"}, {"versioned_ensembl_gene_id":"ENSG00000281903.2","gene_symbol":"LINC02246","gene_name":"long intergenic non-protein coding RNA 2246 [Source:HGNC Symbol;Acc:HGNC:53135]","synonyms":"ENST00000418954","biotype":"lincRNA","ncbi_id":"107987295","summary":null,"start":14819699,"end":14918552,"strand":-1,"description":"long intergenic non-protein coding RNA 2246 [Source:HGNC Symbol;Acc:HGNC:53135]"}, {"versioned_ensembl_gene_id":"ENSG00000158008.9","gene_symbol":"EXTL1","gene_name":"exostosin like glycosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3515]","synonyms":"EXTL,MGC70794","biotype":"protein_coding","ncbi_id":"2134","summary":"This gene is a member of the multiple exostoses (EXT) family of glycosyltransferases, which function in the chain polymerization of heparan sulfate and heparin. The encoded protein harbors alpha 1,4- N-acetylglucosaminyltransferase activity, and is involved in chain elongation of heparan sulfate and possibly heparin. [provided by RefSeq, Jul 2008]","start":26019884,"end":26036464,"strand":1,"description":"exostosin like glycosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3515]"}, {"versioned_ensembl_gene_id":"ENSG00000251448.1","gene_symbol":"AC063919.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126288867,"end":126294024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282232.1","gene_symbol":"IGHD3-16","gene_name":"immunoglobulin heavy diversity 3-16 [Source:HGNC Symbol;Acc:HGNC:5496]","synonyms":"IGHD316","biotype":"IG_D_gene","ncbi_id":"28498","summary":null,"start":105896405,"end":105896441,"strand":-1,"description":"immunoglobulin heavy diversity 3-16 [Source:HGNC Symbol;Acc:HGNC:5496]"}, {"versioned_ensembl_gene_id":"ENSG00000229886.1","gene_symbol":"AC068533.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66025126,"end":66031544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157884.10","gene_symbol":"CIB4","gene_name":"calcium and integrin binding family member 4 [Source:HGNC Symbol;Acc:HGNC:33703]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130106","summary":null,"start":26581202,"end":26641368,"strand":-1,"description":"calcium and integrin binding family member 4 [Source:HGNC Symbol;Acc:HGNC:33703]"}, {"versioned_ensembl_gene_id":"ENSG00000184434.7","gene_symbol":"LRRC19","gene_name":"leucine rich repeat containing 19 [Source:HGNC Symbol;Acc:HGNC:23379]","synonyms":"FLJ21302","biotype":"protein_coding","ncbi_id":"64922","summary":null,"start":26993136,"end":27005693,"strand":-1,"description":"leucine rich repeat containing 19 [Source:HGNC Symbol;Acc:HGNC:23379]"}, {"versioned_ensembl_gene_id":"ENSG00000223837.2","gene_symbol":"AL645941.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32970232,"end":32970886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236510.1","gene_symbol":"AC011284.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3642815,"end":3643784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235631.1","gene_symbol":"RNF148","gene_name":"ring finger protein 148 [Source:HGNC Symbol;Acc:HGNC:22411]","synonyms":"MGC35222","biotype":"protein_coding","ncbi_id":"378925","summary":null,"start":122701664,"end":122702967,"strand":-1,"description":"ring finger protein 148 [Source:HGNC Symbol;Acc:HGNC:22411]"}, {"versioned_ensembl_gene_id":"ENSG00000231892.1","gene_symbol":"AC073316.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3196626,"end":3198256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281731.2","gene_symbol":"AC110079.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118664087,"end":118685341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233907.1","gene_symbol":"LINC01761","gene_name":"long intergenic non-protein coding RNA 1761 [Source:HGNC Symbol;Acc:HGNC:52551]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440594","summary":null,"start":95474737,"end":95479356,"strand":1,"description":"long intergenic non-protein coding RNA 1761 [Source:HGNC Symbol;Acc:HGNC:52551]"}, {"versioned_ensembl_gene_id":"ENSG00000229302.1","gene_symbol":"TAF9P2","gene_name":"TATA-box binding protein associated factor 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31744]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360003","summary":null,"start":18276607,"end":18277495,"strand":-1,"description":"TATA-box binding protein associated factor 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31744]"}, {"versioned_ensembl_gene_id":"ENSG00000233642.1","gene_symbol":"GPR158-AS1","gene_name":"GPR158 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44163]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128811","summary":null,"start":25158072,"end":25176276,"strand":-1,"description":"GPR158 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44163]"}, {"versioned_ensembl_gene_id":"ENSG00000162639.15","gene_symbol":"HENMT1","gene_name":"HEN methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26400]","synonyms":"HEN1,FLJ30525,C1orf59","biotype":"protein_coding","ncbi_id":"113802","summary":null,"start":108648290,"end":108661526,"strand":-1,"description":"HEN methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26400]"}, {"versioned_ensembl_gene_id":"ENSG00000084623.11","gene_symbol":"EIF3I","gene_name":"eukaryotic translation initiation factor 3 subunit I [Source:HGNC Symbol;Acc:HGNC:3272]","synonyms":"TRIP-1,EIF3S2,eIF3i,eIF3-p36,eIF3-beta","biotype":"protein_coding","ncbi_id":"8668","summary":null,"start":32221928,"end":32231604,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit I [Source:HGNC Symbol;Acc:HGNC:3272]"}, {"versioned_ensembl_gene_id":"ENSG00000235301.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32896416,"end":32896490,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000283431.1","gene_symbol":"AC099654.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57163168,"end":57166024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277132.2","gene_symbol":"UGT2B15","gene_name":"UDP glucuronosyltransferase family 2 member B15 [Source:HGNC Symbol;Acc:HGNC:12546]","synonyms":"UGT2B8","biotype":"protein_coding","ncbi_id":"7366","summary":"This gene encodes a glycosyltransferase that is invovled in the metabolism and elimination of toxic compounts, both endogenous and of xenobiotic origin. This gene plays a role in the regulation of estrogens and androgens. This locus is present in a cluster of similar genes and pseudogenes on chromosome 4. [provided by RefSeq, Aug 2016]","start":68529322,"end":68553341,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B15 [Source:HGNC Symbol;Acc:HGNC:12546]"}, {"versioned_ensembl_gene_id":"ENSG00000213888.3","gene_symbol":"LINC01521","gene_name":"long intergenic non-protein coding RNA 1521 [Source:HGNC Symbol;Acc:HGNC:26029]","synonyms":null,"biotype":"lincRNA","ncbi_id":"54944","summary":null,"start":31346777,"end":31348719,"strand":1,"description":"long intergenic non-protein coding RNA 1521 [Source:HGNC Symbol;Acc:HGNC:26029]"}, {"versioned_ensembl_gene_id":"ENSG00000203883.6","gene_symbol":"SOX18","gene_name":"SRY-box 18 [Source:HGNC Symbol;Acc:HGNC:11194]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54345","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. [provided by RefSeq, Jul 2008]","start":64047582,"end":64049641,"strand":-1,"description":"SRY-box 18 [Source:HGNC Symbol;Acc:HGNC:11194]"}, {"versioned_ensembl_gene_id":"ENSG00000113163.15","gene_symbol":"COL4A3BP","gene_name":"collagen type IV alpha 3 binding protein [Source:HGNC Symbol;Acc:HGNC:2205]","synonyms":"STARD11,GPBP,CERT","biotype":"protein_coding","ncbi_id":"10087","summary":"This gene encodes a kinase that specifically phosphorylates the N-terminal region of the non-collagenous domain of the alpha 3 chain of type IV collagen, known as the Goodpasture antigen. Goodpasture disease is the result of an autoimmune response directed at this antigen. One isoform of this protein is also involved in ceramide intracellular transport. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75368486,"end":75512138,"strand":-1,"description":"collagen type IV alpha 3 binding protein [Source:HGNC Symbol;Acc:HGNC:2205]"}, {"versioned_ensembl_gene_id":"ENSG00000281547.1","gene_symbol":"UGT2B29P","gene_name":"UDP glucuronosyltransferase family 2 member B29, pseudogene [Source:HGNC Symbol;Acc:HGNC:12552]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"54568","summary":null,"start":68509485,"end":68511653,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B29, pseudogene [Source:HGNC Symbol;Acc:HGNC:12552]"}, {"versioned_ensembl_gene_id":"ENSG00000188585.8","gene_symbol":"CLEC20A","gene_name":"C-type lectin domain containing 20A [Source:HGNC Symbol;Acc:HGNC:34521]","synonyms":"RP4-593C16.2,NCRNA00083,LINC00083,FLJ44005","biotype":"protein_coding","ncbi_id":"400797","summary":null,"start":178479247,"end":178499634,"strand":-1,"description":"C-type lectin domain containing 20A [Source:HGNC Symbol;Acc:HGNC:34521]"}, {"versioned_ensembl_gene_id":"ENSG00000274405.4","gene_symbol":"SPAG11B","gene_name":"sperm associated antigen 11B [Source:HGNC Symbol;Acc:HGNC:14534]","synonyms":"HE2,EP2D,EP2C,EP2,EDDM2B","biotype":"protein_coding","ncbi_id":"10407","summary":"This gene encodes several androgen-dependent, epididymis-specific secretory proteins. The specific functions of these proteins have not been determined, but they are thought to be involved in sperm maturation. Some of the isoforms contain regions of similarity to beta-defensins, a family of antimicrobial peptides. The gene is located on chromosome 8p23 near the defensin gene cluster. Alternative splicing of this gene results in seven transcript variants encoding different isoforms. Two different N-terminal and five different C-terminal protein sequences are encoded by the splice variants. Two additional variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]","start":7434631,"end":7455657,"strand":-1,"description":"sperm associated antigen 11B [Source:HGNC Symbol;Acc:HGNC:14534]"}, {"versioned_ensembl_gene_id":"ENSG00000267564.1","gene_symbol":"AP001109.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11447756,"end":11489369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168476.11","gene_symbol":"REEP4","gene_name":"receptor accessory protein 4 [Source:HGNC Symbol;Acc:HGNC:26176]","synonyms":"C8orf20,Yip2c,PP432,FLJ22277,FLJ22246","biotype":"protein_coding","ncbi_id":"80346","summary":null,"start":22138020,"end":22141951,"strand":-1,"description":"receptor accessory protein 4 [Source:HGNC Symbol;Acc:HGNC:26176]"}, {"versioned_ensembl_gene_id":"ENSG00000234349.1","gene_symbol":"GLUD1P9","gene_name":"glutamate dehydrogenase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131281","summary":null,"start":111229889,"end":111231061,"strand":-1,"description":"glutamate dehydrogenase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37696]"}, {"versioned_ensembl_gene_id":"ENSG00000280099.1","gene_symbol":"AL603750.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85152487,"end":85154203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122585.7","gene_symbol":"NPY","gene_name":"neuropeptide Y [Source:HGNC Symbol;Acc:HGNC:7955]","synonyms":"PYY4","biotype":"protein_coding","ncbi_id":"4852","summary":"This gene encodes a neuropeptide that is widely expressed in the central nervous system and influences many physiological processes, including cortical excitability, stress response, food intake, circadian rhythms, and cardiovascular function. The neuropeptide functions through G protein-coupled receptors to inhibit adenylyl cyclase, activate mitogen-activated protein kinase (MAPK), regulate intracellular calcium levels, and activate potassium channels. A polymorphism in this gene resulting in a change of leucine 7 to proline in the signal peptide is associated with elevated cholesterol levels, higher alcohol consumption, and may be a risk factor for various metabolic and cardiovascular diseases. The protein also exhibits antimicrobial activity against bacteria and fungi. [provided by RefSeq, Oct 2014]","start":24284163,"end":24291865,"strand":1,"description":"neuropeptide Y [Source:HGNC Symbol;Acc:HGNC:7955]"}, {"versioned_ensembl_gene_id":"ENSG00000265204.1","gene_symbol":"AC090772.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24076794,"end":24099320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281561.1","gene_symbol":"AF252830.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7334978,"end":7336158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227930.1","gene_symbol":"AC003087.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23891704,"end":23897335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260382.1","gene_symbol":"AC087481.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30882267,"end":30883231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126603.8","gene_symbol":"GLIS2","gene_name":"GLIS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:29450]","synonyms":"NPHP7","biotype":"protein_coding","ncbi_id":"84662","summary":"This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010]","start":4314761,"end":4339597,"strand":1,"description":"GLIS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:29450]"}, {"versioned_ensembl_gene_id":"ENSG00000281392.1","gene_symbol":"LINC00506","gene_name":"long intergenic non-protein coding RNA 506 [Source:NCBI gene;Acc:100846978]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100846978","summary":null,"start":87089129,"end":87157069,"strand":1,"description":"long intergenic non-protein coding RNA 506 [Source:NCBI gene;Acc:100846978]"}, {"versioned_ensembl_gene_id":"ENSG00000224003.1","gene_symbol":"YES1P1","gene_name":"YES1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12842]","synonyms":"YESP,YES2,SYR,D22S670","biotype":"processed_pseudogene","ncbi_id":"7526","summary":null,"start":25647261,"end":25649232,"strand":1,"description":"YES1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12842]"}, {"versioned_ensembl_gene_id":"ENSG00000223662.1","gene_symbol":"SAMSN1-AS1","gene_name":"SAMSN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39599]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874190","summary":null,"start":14582202,"end":14598303,"strand":1,"description":"SAMSN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39599]"}, {"versioned_ensembl_gene_id":"ENSG00000159131.16","gene_symbol":"GART","gene_name":"phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Source:HGNC Symbol;Acc:HGNC:4163]","synonyms":"PRGS,PGFT","biotype":"protein_coding","ncbi_id":"2618","summary":"The protein encoded by this gene is a trifunctional polypeptide. It has phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase activity which is required for de novo purine biosynthesis. This enzyme is highly conserved in vertebrates. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33503931,"end":33543491,"strand":-1,"description":"phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Source:HGNC Symbol;Acc:HGNC:4163]"}, {"versioned_ensembl_gene_id":"ENSG00000109063.14","gene_symbol":"MYH3","gene_name":"myosin heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:7573]","synonyms":"SMHCE,MYHSE1,MYHC-EMB,HEMHC","biotype":"protein_coding","ncbi_id":"4621","summary":"Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]","start":10628526,"end":10657309,"strand":-1,"description":"myosin heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:7573]"}, {"versioned_ensembl_gene_id":"ENSG00000230671.2","gene_symbol":"NDUFS5P5","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128177","summary":null,"start":118400514,"end":118400834,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44043]"}, {"versioned_ensembl_gene_id":"ENSG00000253400.1","gene_symbol":"AL356133.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26801733,"end":26805862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279256.1","gene_symbol":"AL442639.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":26642697,"end":26644595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075785.12","gene_symbol":"RAB7A","gene_name":"RAB7A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9788]","synonyms":"RAB7","biotype":"protein_coding","ncbi_id":"7879","summary":"RAB family members are small, RAS-related GTP-binding proteins that are important regulators of vesicular transport. Each RAB protein targets multiple proteins that act in exocytic / endocytic pathways. This gene encodes a RAB family member that regulates vesicle traffic in the late endosomes and also from late endosomes to lysosomes. This encoded protein is also involved in the cellular vacuolation of the VacA cytotoxin of Helicobacter pylori. Mutations at highly conserved amino acid residues in this gene have caused some forms of Charcot-Marie-Tooth (CMT) type 2 neuropathies. [provided by RefSeq, Jul 2008]","start":128726122,"end":128814796,"strand":1,"description":"RAB7A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9788]"}, {"versioned_ensembl_gene_id":"ENSG00000278855.2","gene_symbol":"KCNQ1DN","gene_name":"KCNQ1 downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13335]","synonyms":"HSA404617,BWRT","biotype":"antisense_RNA","ncbi_id":"55539","summary":"Imprinting is a phenomenon in which epigenetic modifications lead to expression or suppression of alleles of some genes based on their parental origin. Wilms tumor-2 (WT2; MIM 194071) is defined by maternal-specific loss of heterozygosity of a critical region on chromosome 11p15.5 that includes several imprinted genes. KCNQ1DN is an imprinted gene located within the WT2 critical region that is expressed from the maternal allele (Xin et al., 2000 [PubMed 11056398]).[supplied by OMIM, Mar 2008]","start":2870047,"end":2872091,"strand":1,"description":"KCNQ1 downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13335]"}, {"versioned_ensembl_gene_id":"ENSG00000172640.3","gene_symbol":"OR10AD1","gene_name":"olfactory receptor family 10 subfamily AD member 1 [Source:HGNC Symbol;Acc:HGNC:14819]","synonyms":"OR10AD1P","biotype":"protein_coding","ncbi_id":"121275","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48202083,"end":48203387,"strand":-1,"description":"olfactory receptor family 10 subfamily AD member 1 [Source:HGNC Symbol;Acc:HGNC:14819]"}, {"versioned_ensembl_gene_id":"ENSG00000273107.1","gene_symbol":"AL512598.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24953241,"end":24953513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213548.3","gene_symbol":"AC005522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76361768,"end":76362113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276425.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"nkat5,183ActI,CD158J,cl-49","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738476,"end":54752501,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000260743.1","gene_symbol":"AC007823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179340322,"end":179341887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128610.11","gene_symbol":"FEZF1","gene_name":"FEZ family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:22788]","synonyms":"ZNF312B","biotype":"protein_coding","ncbi_id":"389549","summary":"This gene encodes a transcriptional repressor that belongs to the zinc finger double domain protein family. The encoded protein is thought to play a role in the embryonic migration of gonadotropin-releasing hormone neurons into the brain. Mutations in this gene are associated with hypogonadotropic hypogonadism-22 with anosmia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":122301394,"end":122310691,"strand":-1,"description":"FEZ family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:22788]"}, {"versioned_ensembl_gene_id":"ENSG00000232459.1","gene_symbol":"AC107977.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101828741,"end":101829679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215464.4","gene_symbol":"AP000354.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24269346,"end":24270134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224770.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTN7,HSBLMHC1,BTL-II,HSBLMHC1,BTL-II,BTN7","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32342174,"end":32355327,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000269974.1","gene_symbol":"AC091057.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30648797,"end":30649529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269930.1","gene_symbol":"AC091057.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30616958,"end":30617749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234797.5","gene_symbol":"RPS3AP6","gene_name":"ribosomal protein S3A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"145767","summary":null,"start":59768352,"end":59769146,"strand":1,"description":"ribosomal protein S3A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:18630]"}, {"versioned_ensembl_gene_id":"ENSG00000254995.4","gene_symbol":"STX16-NPEPL1","gene_name":"STX16-NPEPL1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534593","summary":"This locus represents naturally occurring read-through transcription between the neighboring syntaxin 16 (STX16) and aminopeptidase-like 1 (NPEPL1) genes on chromosome 20. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":58651434,"end":58715410,"strand":1,"description":"STX16-NPEPL1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41993]"}, {"versioned_ensembl_gene_id":"ENSG00000141644.17","gene_symbol":"MBD1","gene_name":"methyl-CpG binding domain protein 1 [Source:HGNC Symbol;Acc:HGNC:6916]","synonyms":"PCM1,CXXC3","biotype":"protein_coding","ncbi_id":"4152","summary":"The protein encoded by this gene is a member of a family of nuclear proteins related by the presence of a methyl-CpG binding domain (MBD). These proteins are capable of binding specifically to methylated DNA, and some members can also repress transcription from methylated gene promoters. This protein contains multiple domains: MBD at the N-terminus that functions both in binding to methylated DNA and in protein interactions; several CXXC-type zinc finger domains that mediate binding to non-methylated CpG dinucleotides; transcriptional repression domain (TRD) at the C-terminus that is involved in transcription repression and in protein interactions. Numerous alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Feb 2011]","start":50266882,"end":50281774,"strand":-1,"description":"methyl-CpG binding domain protein 1 [Source:HGNC Symbol;Acc:HGNC:6916]"}, {"versioned_ensembl_gene_id":"ENSG00000254419.1","gene_symbol":"AL139349.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58710795,"end":58711633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248762.2","gene_symbol":"AC012339.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95986108,"end":95993103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227252.1","gene_symbol":"AC105760.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":237059434,"end":237085817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229205.2","gene_symbol":"LINC00200","gene_name":"long intergenic non-protein coding RNA 200 [Source:HGNC Symbol;Acc:HGNC:30974]","synonyms":"NCRNA00200,FLJ40354,C10orf139","biotype":"lincRNA","ncbi_id":"399706","summary":null,"start":1159768,"end":1164672,"strand":1,"description":"long intergenic non-protein coding RNA 200 [Source:HGNC Symbol;Acc:HGNC:30974]"}, {"versioned_ensembl_gene_id":"ENSG00000243312.3","gene_symbol":"AC093827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86870191,"end":86871404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236634.1","gene_symbol":"AC016903.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204470076,"end":204473837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249050.1","gene_symbol":"AC021242.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9453698,"end":9457418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047644.18","gene_symbol":"WWC3","gene_name":"WWC family member 3 [Source:HGNC Symbol;Acc:HGNC:29237]","synonyms":"KIAA1280,BM042","biotype":"protein_coding","ncbi_id":"55841","summary":"This gene encodes a member of the WWC family of proteins, which also includes the WWC1 (KIBRA) gene product and the WWC2 gene product. The protein encoded by this gene includes a C2 domain, which is known to mediate homodimerization in the related WWC1 gene product. [provided by RefSeq, Sep 2011]","start":10015562,"end":10144478,"strand":1,"description":"WWC family member 3 [Source:HGNC Symbol;Acc:HGNC:29237]"}, {"versioned_ensembl_gene_id":"ENSG00000189051.5","gene_symbol":"RNF222","gene_name":"ring finger protein 222 [Source:HGNC Symbol;Acc:HGNC:34517]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643904","summary":null,"start":8390704,"end":8397826,"strand":-1,"description":"ring finger protein 222 [Source:HGNC Symbol;Acc:HGNC:34517]"}, {"versioned_ensembl_gene_id":"ENSG00000231546.1","gene_symbol":"RPL3P5","gene_name":"ribosomal protein L3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36934]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100130450","summary":null,"start":236407846,"end":236409077,"strand":-1,"description":"ribosomal protein L3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36934]"}, {"versioned_ensembl_gene_id":"ENSG00000232893.1","gene_symbol":"IQCA1-AS1","gene_name":"IQCA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41137]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107080627","summary":null,"start":236391074,"end":236392388,"strand":1,"description":"IQCA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41137]"}, {"versioned_ensembl_gene_id":"ENSG00000233490.7","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"G18.1a,G18.2,AGS4,G18,G18.1b,NG1,C6orf9","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32139234,"end":32143991,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000175879.8","gene_symbol":"HOXD8","gene_name":"homeobox D8 [Source:HGNC Symbol;Acc:HGNC:5139]","synonyms":"HOX4E,HOX4","biotype":"protein_coding","ncbi_id":"3234","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. In addition to effects during embryogenesis, this particular gene may also play a role in adult urogenital tract function. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]","start":176129694,"end":176132695,"strand":1,"description":"homeobox D8 [Source:HGNC Symbol;Acc:HGNC:5139]"}, {"versioned_ensembl_gene_id":"ENSG00000224777.3","gene_symbol":"OR4F2P","gene_name":"olfactory receptor family 4 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8299]","synonyms":"S191N21,OR4F2,hs6M1-11","biotype":"unprocessed_pseudogene","ncbi_id":"390028","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":86649,"end":87586,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8299]"}, {"versioned_ensembl_gene_id":"ENSG00000236653.2","gene_symbol":"LINC01923","gene_name":"long intergenic non-protein coding RNA 1923 [Source:HGNC Symbol;Acc:HGNC:52742]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927619","summary":null,"start":198299363,"end":198375116,"strand":-1,"description":"long intergenic non-protein coding RNA 1923 [Source:HGNC Symbol;Acc:HGNC:52742]"}, {"versioned_ensembl_gene_id":"ENSG00000263231.1","gene_symbol":"AC217785.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155229777,"end":155234285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246740.2","gene_symbol":"PLA2G4E-AS1","gene_name":"PLA2G4E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51419]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928388","summary":null,"start":41972763,"end":41999094,"strand":1,"description":"PLA2G4E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51419]"}, {"versioned_ensembl_gene_id":"ENSG00000119535.17","gene_symbol":"CSF3R","gene_name":"colony stimulating factor 3 receptor [Source:HGNC Symbol;Acc:HGNC:2439]","synonyms":"GCSFR,CD114","biotype":"protein_coding","ncbi_id":"1441","summary":"The protein encoded by this gene is the receptor for colony stimulating factor 3, a cytokine that controls the production, differentiation, and function of granulocytes. The encoded protein, which is a member of the family of cytokine receptors, may also function in some cell surface adhesion or recognition processes. Alternatively spliced transcript variants have been described. Mutations in this gene are a cause of Kostmann syndrome, also known as severe congenital neutropenia. [provided by RefSeq, Aug 2010]","start":36466043,"end":36483278,"strand":-1,"description":"colony stimulating factor 3 receptor [Source:HGNC Symbol;Acc:HGNC:2439]"}, {"versioned_ensembl_gene_id":"ENSG00000139291.13","gene_symbol":"TMEM19","gene_name":"transmembrane protein 19 [Source:HGNC Symbol;Acc:HGNC:25605]","synonyms":"FLJ10936","biotype":"protein_coding","ncbi_id":"55266","summary":null,"start":71686087,"end":71705046,"strand":1,"description":"transmembrane protein 19 [Source:HGNC Symbol;Acc:HGNC:25605]"}, {"versioned_ensembl_gene_id":"ENSG00000248745.2","gene_symbol":"NMNAT1P4","gene_name":"NMNAT1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49166]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132841","summary":null,"start":145456005,"end":145456844,"strand":1,"description":"NMNAT1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49166]"}, {"versioned_ensembl_gene_id":"ENSG00000225452.5","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"RING5,RMA1,NG2,G16","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32254782,"end":32257219,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000141068.13","gene_symbol":"KSR1","gene_name":"kinase suppressor of ras 1 [Source:HGNC Symbol;Acc:HGNC:6465]","synonyms":"RSU2,KSR","biotype":"protein_coding","ncbi_id":"8844","summary":null,"start":27456714,"end":27626438,"strand":1,"description":"kinase suppressor of ras 1 [Source:HGNC Symbol;Acc:HGNC:6465]"}, {"versioned_ensembl_gene_id":"ENSG00000070718.11","gene_symbol":"AP3M2","gene_name":"adaptor related protein complex 3 mu 2 subunit [Source:HGNC Symbol;Acc:HGNC:570]","synonyms":"CLA20,AP47B","biotype":"protein_coding","ncbi_id":"10947","summary":"This gene encodes a subunit of the heterotetrameric adaptor-related protein comlex 3 (AP-3), which belongs to the adaptor complexes medium subunits family. The AP-3 complex plays a role in protein trafficking to lysosomes and specialized organelles. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2008]","start":42152946,"end":42171673,"strand":1,"description":"adaptor related protein complex 3 mu 2 subunit [Source:HGNC Symbol;Acc:HGNC:570]"}, {"versioned_ensembl_gene_id":"ENSG00000265801.1","gene_symbol":"AC069366.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27465112,"end":27465541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259654.1","gene_symbol":"AC115102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84685884,"end":84686946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282507.1","gene_symbol":"AC236756.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157741015,"end":157742461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172294.7","gene_symbol":"CSPG4P4Y","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38535]","synonyms":"CSPG4P7Y,CSPG4P4","biotype":"unprocessed_pseudogene","ncbi_id":"100287502","summary":null,"start":25478269,"end":25483630,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:38535]"}, {"versioned_ensembl_gene_id":"ENSG00000233619.1","gene_symbol":"AC006328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25487284,"end":25487662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232671.5","gene_symbol":"AL391069.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151280024,"end":151281929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133393.12","gene_symbol":"FOPNL","gene_name":"FGFR1OP N-terminal like [Source:HGNC Symbol;Acc:HGNC:26435]","synonyms":"PHSECRG2,FOR20,FLJ31153,DKFZp686N1651,C16orf63","biotype":"protein_coding","ncbi_id":"123811","summary":null,"start":15865720,"end":15888625,"strand":-1,"description":"FGFR1OP N-terminal like [Source:HGNC Symbol;Acc:HGNC:26435]"}, {"versioned_ensembl_gene_id":"ENSG00000253232.1","gene_symbol":"AC091144.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33523154,"end":33523291,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145063.14","gene_symbol":"AC062028.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11105317,"end":11132821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253735.1","gene_symbol":"AC021736.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9351238,"end":9358441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244752.2","gene_symbol":"CRYBB2","gene_name":"crystallin beta B2 [Source:HGNC Symbol;Acc:HGNC:2398]","synonyms":"CRYB2A,CRYB2,CCA2","biotype":"protein_coding","ncbi_id":"1415","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta basic group member, is part of a gene cluster with beta-A4, beta-B1, and beta-B3. A chain-terminating mutation was found to cause type 2 cerulean cataracts. [provided by RefSeq, Jul 2008]","start":25219522,"end":25231869,"strand":1,"description":"crystallin beta B2 [Source:HGNC Symbol;Acc:HGNC:2398]"}, {"versioned_ensembl_gene_id":"ENSG00000172297.7","gene_symbol":"GOLGA2P3Y","gene_name":"golgin A2 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:32426]","synonyms":"GOLGA2P3,GOLGA2LY2","biotype":"unprocessed_pseudogene","ncbi_id":"401634","summary":"There are two copies of this pseudogene within the P1 palindrome on chromosome Y. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":25454561,"end":25460572,"strand":1,"description":"golgin A2 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:32426]"}, {"versioned_ensembl_gene_id":"ENSG00000272727.1","gene_symbol":"LINC02266","gene_name":"long intergenic non-protein coding RNA 2266 [Source:HGNC Symbol;Acc:HGNC:53180]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377466","summary":null,"start":145335263,"end":145340421,"strand":-1,"description":"long intergenic non-protein coding RNA 2266 [Source:HGNC Symbol;Acc:HGNC:53180]"}, {"versioned_ensembl_gene_id":"ENSG00000240992.1","gene_symbol":"RPS23P4","gene_name":"ribosomal protein S23 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36633]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271092","summary":null,"start":145269810,"end":145270558,"strand":-1,"description":"ribosomal protein S23 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36633]"}, {"versioned_ensembl_gene_id":"ENSG00000275997.1","gene_symbol":"AC016292.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1155966,"end":1156175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000039537.13","gene_symbol":"C6","gene_name":"complement C6 [Source:HGNC Symbol;Acc:HGNC:1339]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729","summary":"This gene encodes a component of the complement cascade. The encoded protein is part of the membrane attack complex that can be incorporated into the cell membrane and cause cell lysis. Mutations in this gene are associated with complement component-6 deficiency. Transcript variants encoding the same protein have been described.[provided by RefSeq, Nov 2012]","start":41142234,"end":41261438,"strand":-1,"description":"complement C6 [Source:HGNC Symbol;Acc:HGNC:1339]"}, {"versioned_ensembl_gene_id":"ENSG00000198367.3","gene_symbol":"OR7A11P","gene_name":"olfactory receptor family 7 subfamily A member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:8357]","synonyms":"OST527,OR7A11","biotype":"unprocessed_pseudogene","ncbi_id":"26669","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14916428,"end":14917380,"strand":1,"description":"olfactory receptor family 7 subfamily A member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:8357]"}, {"versioned_ensembl_gene_id":"ENSG00000281050.1","gene_symbol":"KRT18P53","gene_name":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478925","summary":null,"start":544216,"end":544332,"strand":-1,"description":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]"}, {"versioned_ensembl_gene_id":"ENSG00000169967.16","gene_symbol":"MAP3K2","gene_name":"mitogen-activated protein kinase kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6854]","synonyms":"MEKK2B,MEKK2","biotype":"protein_coding","ncbi_id":"10746","summary":"The protein encoded by this gene is a member of serine/threonine protein kinase family. This kinase preferentially activates other kinases involved in the MAP kinase signaling pathway. This kinase has been shown to directly phosphorylate and activate Ikappa B kinases, and thus plays a role in NF-kappa B signaling pathway. This kinase has also been found to bind and activate protein kinase C-related kinase 2, which suggests its involvement in a regulated signaling process. [provided by RefSeq, Jul 2008]","start":127298730,"end":127388465,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6854]"}, {"versioned_ensembl_gene_id":"ENSG00000251171.1","gene_symbol":"AC096741.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169201794,"end":169220349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251177.2","gene_symbol":"AC093829.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69572391,"end":69585527,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000015153.14","gene_symbol":"YAF2","gene_name":"YY1 associated factor 2 [Source:HGNC Symbol;Acc:HGNC:17363]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10138","summary":"This gene encodes a zinc finger containing protein that functions in the regulation of transcription. This protein was identified as an interacting partner of transcriptional repressor protein Yy1, and also interacts with other transcriptional regulators, including Myc and Polycomb. This protein can promote proteolysis of Yy1. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2016]","start":42157104,"end":42238349,"strand":-1,"description":"YY1 associated factor 2 [Source:HGNC Symbol;Acc:HGNC:17363]"}, {"versioned_ensembl_gene_id":"ENSG00000137265.14","gene_symbol":"IRF4","gene_name":"interferon regulatory factor 4 [Source:HGNC Symbol;Acc:HGNC:6119]","synonyms":"MUM1,LSIRF","biotype":"protein_coding","ncbi_id":"3662","summary":"The protein encoded by this gene belongs to the IRF (interferon regulatory factor) family of transcription factors, characterized by an unique tryptophan pentad repeat DNA-binding domain. The IRFs are important in the regulation of interferons in response to infection by virus, and in the regulation of interferon-inducible genes. This family member is lymphocyte specific and negatively regulates Toll-like-receptor (TLR) signaling that is central to the activation of innate and adaptive immune systems. A chromosomal translocation involving this gene and the IgH locus, t(6;14)(p25;q32), may be a cause of multiple myeloma. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2010]","start":391739,"end":411447,"strand":1,"description":"interferon regulatory factor 4 [Source:HGNC Symbol;Acc:HGNC:6119]"}, {"versioned_ensembl_gene_id":"ENSG00000205318.5","gene_symbol":"GCNT6","gene_name":"glucosaminyl (N-acetyl) transferase 6 [Source:HGNC Symbol;Acc:HGNC:21623]","synonyms":"bA421M1.3","biotype":"processed_pseudogene","ncbi_id":"644378","summary":null,"start":10633762,"end":10634695,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 6 [Source:HGNC Symbol;Acc:HGNC:21623]"}, {"versioned_ensembl_gene_id":"ENSG00000233575.2","gene_symbol":"AL358934.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1328664,"end":1328987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243245.1","gene_symbol":"BX248406.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32748582,"end":32751171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274899.1","gene_symbol":"AC006386.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25174520,"end":25175237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160741.16","gene_symbol":"CRTC2","gene_name":"CREB regulated transcription coactivator 2 [Source:HGNC Symbol;Acc:HGNC:27301]","synonyms":"TORC2","biotype":"protein_coding","ncbi_id":"200186","summary":"This gene encodes a member of the transducers of regulated cAMP response element-binding protein activity family of transcription coactivators. These proteins promote the transcription of genes targeted by the cAMP response element-binding protein, and therefore play an important role in many cellular processes. Under basal conditions the encoded protein is phosphorylated by AMP-activated protein kinase or the salt-inducible kinases and is sequestered in the cytoplasm. Upon activation by elevated cAMP or calcium, the encoded protein translocates to the nucleus and increases target gene expression. Single nucleotide polymorphisms in this gene may increase the risk of type 2 diabetes. A pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2010]","start":153947669,"end":153958625,"strand":-1,"description":"CREB regulated transcription coactivator 2 [Source:HGNC Symbol;Acc:HGNC:27301]"}, {"versioned_ensembl_gene_id":"ENSG00000137313.15","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30173958,"end":30202936,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000281967.1","gene_symbol":"AC233699.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36234819,"end":36234926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183891.5","gene_symbol":"TTC32","gene_name":"tetratricopeptide repeat domain 32 [Source:HGNC Symbol;Acc:HGNC:32954]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130502","summary":null,"start":19896643,"end":19901986,"strand":-1,"description":"tetratricopeptide repeat domain 32 [Source:HGNC Symbol;Acc:HGNC:32954]"}, {"versioned_ensembl_gene_id":"ENSG00000145321.12","gene_symbol":"GC","gene_name":"GC, vitamin D binding protein [Source:HGNC Symbol;Acc:HGNC:4187]","synonyms":"VDBP,hDBP,DBP","biotype":"protein_coding","ncbi_id":"2638","summary":"The protein encoded by this gene belongs to the albumin gene family. It is a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid and on the surface of many cell types. It binds to vitamin D and its plasma metabolites and transports them to target tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]","start":71741693,"end":71804041,"strand":-1,"description":"GC, vitamin D binding protein [Source:HGNC Symbol;Acc:HGNC:4187]"}, {"versioned_ensembl_gene_id":"ENSG00000240034.1","gene_symbol":"MTND6P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39469]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478944","summary":null,"start":106900593,"end":106900855,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39469]"}, {"versioned_ensembl_gene_id":"ENSG00000267688.1","gene_symbol":"KF456478.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3121116,"end":3122128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249580.1","gene_symbol":"MTATP6P22","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52178]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075202","summary":null,"start":106897671,"end":106898268,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52178]"}, {"versioned_ensembl_gene_id":"ENSG00000088256.8","gene_symbol":"GNA11","gene_name":"G protein subunit alpha 11 [Source:HGNC Symbol;Acc:HGNC:4379]","synonyms":"FHH2,FBH2,FBH,HHC2","biotype":"protein_coding","ncbi_id":"2767","summary":"The protein encoded by this gene belongs to the family of guanine nucleotide-binding proteins (G proteins), which function as modulators or transducers in various transmembrane signaling systems. G proteins are composed of 3 units: alpha, beta and gamma. This gene encodes one of the alpha subunits (subunit alpha-11). Mutations in this gene have been associated with hypocalciuric hypercalcemia type II (HHC2) and hypocalcemia dominant 2 (HYPOC2). Patients with HHC2 and HYPOC2 exhibit decreased or increased sensitivity, respectively, to changes in extracellular calcium concentrations. [provided by RefSeq, Dec 2013]","start":3094410,"end":3124004,"strand":1,"description":"G protein subunit alpha 11 [Source:HGNC Symbol;Acc:HGNC:4379]"}, {"versioned_ensembl_gene_id":"ENSG00000165449.11","gene_symbol":"SLC16A9","gene_name":"solute carrier family 16 member 9 [Source:HGNC Symbol;Acc:HGNC:23520]","synonyms":"MCT9,FLJ43803,C10orf36","biotype":"protein_coding","ncbi_id":"220963","summary":null,"start":59650761,"end":59736002,"strand":-1,"description":"solute carrier family 16 member 9 [Source:HGNC Symbol;Acc:HGNC:23520]"}, {"versioned_ensembl_gene_id":"ENSG00000242836.1","gene_symbol":"MTCO3P35","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52138]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075287","summary":null,"start":106896891,"end":106897671,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52138]"}, {"versioned_ensembl_gene_id":"ENSG00000242759.6","gene_symbol":"LINC00882","gene_name":"long intergenic non-protein coding RNA 882 [Source:HGNC Symbol;Acc:HGNC:48568]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100302640","summary":null,"start":106836811,"end":107240641,"strand":-1,"description":"long intergenic non-protein coding RNA 882 [Source:HGNC Symbol;Acc:HGNC:48568]"}, {"versioned_ensembl_gene_id":"ENSG00000256210.3","gene_symbol":"AC005255.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14792318,"end":14792533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188269.9","gene_symbol":"OR7A5","gene_name":"olfactory receptor family 7 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:8368]","synonyms":"HTPCR2","biotype":"protein_coding","ncbi_id":"26659","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14824251,"end":14835285,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:8368]"}, {"versioned_ensembl_gene_id":"ENSG00000230393.1","gene_symbol":"AC092667.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100104919,"end":100107504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276590.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738496,"end":54752881,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000254119.5","gene_symbol":"AC025524.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61785047,"end":61944180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074319.12","gene_symbol":"TSG101","gene_name":"tumor susceptibility 101 [Source:HGNC Symbol;Acc:HGNC:15971]","synonyms":"VPS23,TSG10","biotype":"protein_coding","ncbi_id":"7251","summary":"The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008]","start":18468336,"end":18527232,"strand":-1,"description":"tumor susceptibility 101 [Source:HGNC Symbol;Acc:HGNC:15971]"}, {"versioned_ensembl_gene_id":"ENSG00000144218.18","gene_symbol":"AFF3","gene_name":"AF4/FMR2 family member 3 [Source:HGNC Symbol;Acc:HGNC:6473]","synonyms":"MLLT2-like,LAF4","biotype":"protein_coding","ncbi_id":"3899","summary":"This gene encodes a tissue-restricted nuclear transcriptional activator that is preferentially expressed in lymphoid tissue. Isolation of this protein initially defined a highly conserved LAF4/MLLT2 gene family of nuclear transcription factors that may function in lymphoid development and oncogenesis. In some ALL patients, this gene has been found fused to the gene for MLL. Multiple alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Jul 2008]","start":99545419,"end":100142739,"strand":-1,"description":"AF4/FMR2 family member 3 [Source:HGNC Symbol;Acc:HGNC:6473]"}, {"versioned_ensembl_gene_id":"ENSG00000127530.3","gene_symbol":"OR7C1","gene_name":"olfactory receptor family 7 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8373]","synonyms":"OR7C4,OR19-5","biotype":"protein_coding","ncbi_id":"26664","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14789260,"end":14835376,"strand":-1,"description":"olfactory receptor family 7 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:8373]"}, {"versioned_ensembl_gene_id":"ENSG00000264714.1","gene_symbol":"AP005117.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":10724619,"end":10728539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239405.1","gene_symbol":"TMED10P2","gene_name":"transmembrane p24 trafficking protein 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38105]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129727","summary":null,"start":128538020,"end":128538631,"strand":1,"description":"transmembrane p24 trafficking protein 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38105]"}, {"versioned_ensembl_gene_id":"ENSG00000260779.1","gene_symbol":"AP001180.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10661933,"end":10666887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236336.1","gene_symbol":"AL022725.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4774526,"end":4775408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274786.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724451,"end":54736098,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000239455.1","gene_symbol":"AC074043.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107104911,"end":107107000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281216.1","gene_symbol":"KIF26B","gene_name":"kinesin family member 26B [Source:HGNC Symbol;Acc:HGNC:25484]","synonyms":"FLJ10157","biotype":"protein_coding","ncbi_id":"55083","summary":"The protein encoded by this gene is an intracellular motor protein thought to transport organelles along microtubules. The encoded protein is required for kidney development. Elevated levels of this protein have been found in some breast and colorectal cancers. [provided by RefSeq, Mar 2017]","start":245353678,"end":245713153,"strand":1,"description":"kinesin family member 26B [Source:HGNC Symbol;Acc:HGNC:25484]"}, {"versioned_ensembl_gene_id":"ENSG00000240796.1","gene_symbol":"MTND2P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42115]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873223","summary":null,"start":106902173,"end":106902523,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42115]"}, {"versioned_ensembl_gene_id":"ENSG00000241787.1","gene_symbol":"MTND4P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42203]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873241","summary":null,"start":106894352,"end":106895718,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42203]"}, {"versioned_ensembl_gene_id":"ENSG00000239586.1","gene_symbol":"MTND1P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42065]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873213","summary":null,"start":106901068,"end":106901965,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42065]"}, {"versioned_ensembl_gene_id":"ENSG00000239997.1","gene_symbol":"FCF1P3","gene_name":"FCF1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128733","summary":null,"start":106848671,"end":106849260,"strand":1,"description":"FCF1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44615]"}, {"versioned_ensembl_gene_id":"ENSG00000230069.3","gene_symbol":"LRRC37A15P","gene_name":"leucine rich repeat containing 37 member A15, pseudogene [Source:HGNC Symbol;Acc:HGNC:43819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481796","summary":null,"start":102727274,"end":102730721,"strand":-1,"description":"leucine rich repeat containing 37 member A15, pseudogene [Source:HGNC Symbol;Acc:HGNC:43819]"}, {"versioned_ensembl_gene_id":"ENSG00000239632.1","gene_symbol":"MTND4LP3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42265]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075245","summary":null,"start":106895729,"end":106896408,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42265]"}, {"versioned_ensembl_gene_id":"ENSG00000242190.1","gene_symbol":"AC017015.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81762706,"end":81764756,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109323.8","gene_symbol":"MANBA","gene_name":"mannosidase beta [Source:HGNC Symbol;Acc:HGNC:6831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4126","summary":"This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement. [provided by RefSeq, Jul 2008]","start":102631488,"end":102760994,"strand":-1,"description":"mannosidase beta [Source:HGNC Symbol;Acc:HGNC:6831]"}, {"versioned_ensembl_gene_id":"ENSG00000213925.3","gene_symbol":"NPM1P33","gene_name":"nucleophosmin 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45212]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131478","summary":null,"start":203772631,"end":203773502,"strand":-1,"description":"nucleophosmin 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:45212]"}, {"versioned_ensembl_gene_id":"ENSG00000224092.1","gene_symbol":"AL591644.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1977784,"end":1978547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162144.9","gene_symbol":"CYB561A3","gene_name":"cytochrome b561 family member A3 [Source:HGNC Symbol;Acc:HGNC:23014]","synonyms":"CYBASC3","biotype":"protein_coding","ncbi_id":"220002","summary":null,"start":61348745,"end":61362299,"strand":-1,"description":"cytochrome b561 family member A3 [Source:HGNC Symbol;Acc:HGNC:23014]"}, {"versioned_ensembl_gene_id":"ENSG00000251402.3","gene_symbol":"FAM90A25P","gene_name":"family with sequence similarity 90 member A25, pseudogene [Source:HGNC Symbol;Acc:HGNC:32246]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"389633","summary":null,"start":12415080,"end":12418090,"strand":-1,"description":"family with sequence similarity 90 member A25, pseudogene [Source:HGNC Symbol;Acc:HGNC:32246]"}, {"versioned_ensembl_gene_id":"ENSG00000224096.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33171150,"end":33176605,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000239440.5","gene_symbol":"LINC02008","gene_name":"long intergenic non-protein coding RNA 2008 [Source:HGNC Symbol;Acc:HGNC:52844]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377180","summary":null,"start":81986138,"end":82463675,"strand":1,"description":"long intergenic non-protein coding RNA 2008 [Source:HGNC Symbol;Acc:HGNC:52844]"}, {"versioned_ensembl_gene_id":"ENSG00000127515.2","gene_symbol":"OR7A10","gene_name":"olfactory receptor family 7 subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:8356]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390892","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14840466,"end":14848922,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 10 [Source:HGNC Symbol;Acc:HGNC:8356]"}, {"versioned_ensembl_gene_id":"ENSG00000239462.1","gene_symbol":"AC091212.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98902424,"end":99018562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226438.1","gene_symbol":"AL442071.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39249838,"end":39257649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232180.8","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31855884,"end":31871733,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000223641.1","gene_symbol":"TTTY17C","gene_name":"testis-specific transcript, Y-linked 17C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31890]","synonyms":"NCRNA00142","biotype":"lincRNA","ncbi_id":"474152","summary":"There are three copies of this gene on chromosome Y. This record represents the most telomeric copy, which is within the P1 palindrome. [provided by RefSeq, Jul 2008]","start":25183643,"end":25184773,"strand":-1,"description":"testis-specific transcript, Y-linked 17C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31890]"}, {"versioned_ensembl_gene_id":"ENSG00000269552.1","gene_symbol":"OR7A8P","gene_name":"olfactory receptor family 7 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8371]","synonyms":"OR7A9P,OR19-11,HG83,OST042","biotype":"unprocessed_pseudogene","ncbi_id":"26661","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14852032,"end":14852944,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8371]"}, {"versioned_ensembl_gene_id":"ENSG00000227633.1","gene_symbol":"RBMY2YP","gene_name":"RNA binding motif protein, Y-linked, family 2, member Y pseudogene [Source:HGNC Symbol;Acc:HGNC:23902]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379024","summary":null,"start":25266584,"end":25273531,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member Y pseudogene [Source:HGNC Symbol;Acc:HGNC:23902]"}, {"versioned_ensembl_gene_id":"ENSG00000078081.7","gene_symbol":"LAMP3","gene_name":"lysosomal associated membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:14582]","synonyms":"TSC403,LAMP,DCLAMP,DC-LAMP,CD208","biotype":"protein_coding","ncbi_id":"27074","summary":"Dendritic cells (DCs) are the most potent antigen-presenting cells. Immature DCs efficiently capture antigens and differentiate into interdigitating dendritic cells (IDCs) in lymphoid tissues that induce primary T-cell responses (summary by de Saint-Vis et al., 1998 [PubMed 9768752]).[supplied by OMIM, Dec 2010]","start":183122213,"end":183163839,"strand":-1,"description":"lysosomal associated membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:14582]"}, {"versioned_ensembl_gene_id":"ENSG00000241367.1","gene_symbol":"RPL7AP23","gene_name":"ribosomal protein L7a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36884]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271040","summary":null,"start":82319172,"end":82320279,"strand":-1,"description":"ribosomal protein L7a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36884]"}, {"versioned_ensembl_gene_id":"ENSG00000172148.3","gene_symbol":"OR7A2P","gene_name":"olfactory receptor family 7 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8370]","synonyms":"OR7A7,OR7A2,OR19-18,OLF4p,hg1003","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390894","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14863714,"end":14867358,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8370]"}, {"versioned_ensembl_gene_id":"ENSG00000250794.2","gene_symbol":"ALG1L12P","gene_name":"asparagine-linked glycosylation 1-like 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:44381]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421097","summary":null,"start":12421032,"end":12425000,"strand":1,"description":"asparagine-linked glycosylation 1-like 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:44381]"}, {"versioned_ensembl_gene_id":"ENSG00000240476.1","gene_symbol":"LINC00973","gene_name":"long intergenic non-protein coding RNA 973 [Source:HGNC Symbol;Acc:HGNC:48868]","synonyms":"CTD-2021J15.2","biotype":"lincRNA","ncbi_id":"100506377","summary":null,"start":98981058,"end":98983096,"strand":1,"description":"long intergenic non-protein coding RNA 973 [Source:HGNC Symbol;Acc:HGNC:48868]"}, {"versioned_ensembl_gene_id":"ENSG00000188603.18","gene_symbol":"CLN3","gene_name":"CLN3, battenin [Source:HGNC Symbol;Acc:HGNC:2074]","synonyms":"JNCL,BTS,BTN1","biotype":"protein_coding","ncbi_id":"1201","summary":"This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":28474111,"end":28495575,"strand":-1,"description":"CLN3, battenin [Source:HGNC Symbol;Acc:HGNC:2074]"}, {"versioned_ensembl_gene_id":"ENSG00000243710.7","gene_symbol":"CFAP57","gene_name":"cilia and flagella associated protein 57 [Source:HGNC Symbol;Acc:HGNC:26485]","synonyms":"WDR65,FLJ32000","biotype":"protein_coding","ncbi_id":"149465","summary":"This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member is thought to function in craniofacial development, possibly in the fusion of lip and palate. A missense mutation in this gene is associated with Van der Woude syndrome 2. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":43172149,"end":43254358,"strand":1,"description":"cilia and flagella associated protein 57 [Source:HGNC Symbol;Acc:HGNC:26485]"}, {"versioned_ensembl_gene_id":"ENSG00000143847.15","gene_symbol":"PPFIA4","gene_name":"PTPRF interacting protein alpha 4 [Source:HGNC Symbol;Acc:HGNC:9248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8497","summary":"PPFIA4, or liprin-alpha-4, belongs to the liprin-alpha gene family. See liprin-alpha-1 (LIP1, or PPFIA1; MIM 611054) for background on liprins.[supplied by OMIM, Mar 2008]","start":203026498,"end":203078740,"strand":1,"description":"PTPRF interacting protein alpha 4 [Source:HGNC Symbol;Acc:HGNC:9248]"}, {"versioned_ensembl_gene_id":"ENSG00000260528.4","gene_symbol":"FAM157C","gene_name":"family with sequence similarity 157 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34081]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996541","summary":null,"start":90102271,"end":90178344,"strand":1,"description":"family with sequence similarity 157 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34081]"}, {"versioned_ensembl_gene_id":"ENSG00000261033.1","gene_symbol":"AC005730.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20008051,"end":20009234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152242.10","gene_symbol":"C18orf25","gene_name":"chromosome 18 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:28172]","synonyms":"RNF111L1,MGC12909,ARKL1","biotype":"protein_coding","ncbi_id":"147339","summary":null,"start":46173553,"end":46266991,"strand":1,"description":"chromosome 18 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:28172]"}, {"versioned_ensembl_gene_id":"ENSG00000175106.16","gene_symbol":"TVP23C","gene_name":"trans-golgi network vesicle protein 23 homolog C [Source:HGNC Symbol;Acc:HGNC:30453]","synonyms":"FAM18B2,MGC8763","biotype":"protein_coding","ncbi_id":"201158","summary":null,"start":15502264,"end":15563595,"strand":-1,"description":"trans-golgi network vesicle protein 23 homolog C [Source:HGNC Symbol;Acc:HGNC:30453]"}, {"versioned_ensembl_gene_id":"ENSG00000260018.1","gene_symbol":"AC040169.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84117051,"end":84117571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186743.2","gene_symbol":"TPI1P3","gene_name":"triosephosphate isomerase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728402","summary":null,"start":116038756,"end":116039495,"strand":1,"description":"triosephosphate isomerase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38070]"}, {"versioned_ensembl_gene_id":"ENSG00000250806.2","gene_symbol":"AC027315.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100654112,"end":100657970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100522.8","gene_symbol":"GNPNAT1","gene_name":"glucosamine-phosphate N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:19980]","synonyms":"Gpnat1,FLJ10607","biotype":"protein_coding","ncbi_id":"64841","summary":null,"start":52775194,"end":52791668,"strand":-1,"description":"glucosamine-phosphate N-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:19980]"}, {"versioned_ensembl_gene_id":"ENSG00000259254.1","gene_symbol":"AC022405.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40642933,"end":40646857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273957.1","gene_symbol":"AC113385.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":100388853,"end":100389938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254883.1","gene_symbol":"AP003385.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67744322,"end":67744645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216819.1","gene_symbol":"TUBB2BP1","gene_name":"tubulin beta 2B class IIb pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42332]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132153","summary":null,"start":3177044,"end":3179764,"strand":-1,"description":"tubulin beta 2B class IIb pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42332]"}, {"versioned_ensembl_gene_id":"ENSG00000224732.1","gene_symbol":"MAGEA7P","gene_name":"MAGE family member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:6805]","synonyms":"MAGEA7,MAGE7","biotype":"unprocessed_pseudogene","ncbi_id":"4106","summary":null,"start":149808214,"end":149809155,"strand":1,"description":"MAGE family member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:6805]"}, {"versioned_ensembl_gene_id":"ENSG00000094841.13","gene_symbol":"UPRT","gene_name":"uracil phosphoribosyltransferase homolog [Source:HGNC Symbol;Acc:HGNC:28334]","synonyms":"RP11-311P8.3,MGC23937,FUR1,DKFZp781E1243","biotype":"protein_coding","ncbi_id":"139596","summary":"This gene encodes uracil phosphoribosyltransferase, which catalyzes the conversion of uracil and 5-phosphoribosyl-1-R-diphosphate to uridine monophosphate (UMP). This reaction is an important part of nucleotide metabolism, specifically the pyrimidine salvage pathway. The enzyme localizes to the nucleus and cytoplasm. The protein is a potential target for rational design of drugs to treat parasitic infections and cancer. [provided by RefSeq, Nov 2009]","start":75274085,"end":75304600,"strand":1,"description":"uracil phosphoribosyltransferase homolog [Source:HGNC Symbol;Acc:HGNC:28334]"}, {"versioned_ensembl_gene_id":"ENSG00000139624.12","gene_symbol":"CERS5","gene_name":"ceramide synthase 5 [Source:HGNC Symbol;Acc:HGNC:23749]","synonyms":"Trh4,MGC45411,LASS5,FLJ25304","biotype":"protein_coding","ncbi_id":"91012","summary":"This gene encodes a protein that belongs to the TLC (TRAM, LAG1 and CLN8 homology domains) family of proteins. The encoded protein functions in the synthesis of ceramide, a lipid molecule that is involved in a several cellular signaling pathways. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":50129306,"end":50167533,"strand":-1,"description":"ceramide synthase 5 [Source:HGNC Symbol;Acc:HGNC:23749]"}, {"versioned_ensembl_gene_id":"ENSG00000270225.1","gene_symbol":"MTCO2P22","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289404","summary":null,"start":100052859,"end":100053539,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52151]"}, {"versioned_ensembl_gene_id":"ENSG00000249908.2","gene_symbol":"BRD9P2","gene_name":"bromodomain containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51446]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729114","summary":null,"start":767382,"end":768930,"strand":-1,"description":"bromodomain containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51446]"}, {"versioned_ensembl_gene_id":"ENSG00000279693.1","gene_symbol":"AC099521.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":68367325,"end":68370262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249515.1","gene_symbol":"LINC02113","gene_name":"long intergenic non-protein coding RNA 2113 [Source:HGNC Symbol;Acc:HGNC:52967]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724855","summary":null,"start":99549432,"end":99577957,"strand":1,"description":"long intergenic non-protein coding RNA 2113 [Source:HGNC Symbol;Acc:HGNC:52967]"}, {"versioned_ensembl_gene_id":"ENSG00000150244.11","gene_symbol":"TRIM48","gene_name":"tripartite motif containing 48 [Source:HGNC Symbol;Acc:HGNC:19021]","synonyms":"RNF101","biotype":"protein_coding","ncbi_id":"79097","summary":null,"start":55262182,"end":55271119,"strand":1,"description":"tripartite motif containing 48 [Source:HGNC Symbol;Acc:HGNC:19021]"}, {"versioned_ensembl_gene_id":"ENSG00000273108.1","gene_symbol":"AL121929.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103608619,"end":103610050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237172.3","gene_symbol":"B3GNT9","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:28714]","synonyms":"MGC4655","biotype":"protein_coding","ncbi_id":"84752","summary":null,"start":67148105,"end":67151214,"strand":-1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:28714]"}, {"versioned_ensembl_gene_id":"ENSG00000267324.1","gene_symbol":"AC006557.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14143596,"end":14151139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251032.1","gene_symbol":"CUL1P1","gene_name":"cullin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49567]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288463","summary":null,"start":127784618,"end":127787042,"strand":-1,"description":"cullin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49567]"}, {"versioned_ensembl_gene_id":"ENSG00000111790.13","gene_symbol":"FGFR1OP2","gene_name":"FGFR1 oncogene partner 2 [Source:HGNC Symbol;Acc:HGNC:23098]","synonyms":"DKFZp564O1863","biotype":"protein_coding","ncbi_id":"26127","summary":null,"start":26938383,"end":26966650,"strand":1,"description":"FGFR1 oncogene partner 2 [Source:HGNC Symbol;Acc:HGNC:23098]"}, {"versioned_ensembl_gene_id":"ENSG00000144426.18","gene_symbol":"NBEAL1","gene_name":"neurobeachin like 1 [Source:HGNC Symbol;Acc:HGNC:20681]","synonyms":"ALS2CR17,ALS2CR16,MGC164581","biotype":"protein_coding","ncbi_id":"65065","summary":null,"start":203014879,"end":203226378,"strand":1,"description":"neurobeachin like 1 [Source:HGNC Symbol;Acc:HGNC:20681]"}, {"versioned_ensembl_gene_id":"ENSG00000268390.1","gene_symbol":"AC011473.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51043806,"end":51052077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189283.9","gene_symbol":"FHIT","gene_name":"fragile histidine triad [Source:HGNC Symbol;Acc:HGNC:3701]","synonyms":"FRA3B,AP3Aase","biotype":"protein_coding","ncbi_id":"2272","summary":"The protein encoded by this gene is a P1-P3-bis(5'-adenosyl) triphosphate hydrolase involved in purine metabolism. This gene encompasses the common fragile site FRA3B on chromosome 3, where carcinogen-induced damage can lead to translocations and aberrant transcripts. In fact, aberrant transcripts from this gene have been found in about half of all esophageal, stomach, and colon carcinomas. The encoded protein is also a tumor suppressor, as loss of its activity results in replication stress and DNA damage. [provided by RefSeq, Aug 2017]","start":59749310,"end":61251459,"strand":-1,"description":"fragile histidine triad [Source:HGNC Symbol;Acc:HGNC:3701]"}, {"versioned_ensembl_gene_id":"ENSG00000186818.12","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"CD85k,LIR-5,ILT3,HM18,LIR5","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54643889,"end":54670359,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000283141.1","gene_symbol":"AL157832.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129784983,"end":129806971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218499.1","gene_symbol":"AL031003.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138393373,"end":138393544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227374.1","gene_symbol":"AL157832.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129768844,"end":129769435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189431.7","gene_symbol":"RASSF10","gene_name":"Ras association domain family member 10 [Source:HGNC Symbol;Acc:HGNC:33984]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644943","summary":null,"start":13009577,"end":13012106,"strand":1,"description":"Ras association domain family member 10 [Source:HGNC Symbol;Acc:HGNC:33984]"}, {"versioned_ensembl_gene_id":"ENSG00000254842.6","gene_symbol":"LINC02551","gene_name":"long intergenic non-protein coding RNA 2551 [Source:HGNC Symbol;Acc:HGNC:53586]","synonyms":"RP11-890B15.2","biotype":"lincRNA","ncbi_id":"100507431","summary":null,"start":130844191,"end":130865561,"strand":-1,"description":"long intergenic non-protein coding RNA 2551 [Source:HGNC Symbol;Acc:HGNC:53586]"}, {"versioned_ensembl_gene_id":"ENSG00000168439.16","gene_symbol":"STIP1","gene_name":"stress induced phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:11387]","synonyms":"STI1,HOP","biotype":"protein_coding","ncbi_id":"10963","summary":"STIP1 is an adaptor protein that coordinates the functions of HSP70 (see HSPA1A; MIM 140550) and HSP90 (see HSP90AA1; MIM 140571) in protein folding. It is thought to assist in the transfer of proteins from HSP70 to HSP90 by binding both HSP90 and substrate-bound HSP70. STIP1 also stimulates the ATPase activity of HSP70 and inhibits the ATPase activity of HSP90, suggesting that it regulates both the conformations and ATPase cycles of these chaperones (Song and Masison, 2005 [PubMed 16100115]).[supplied by OMIM, Jul 2009]","start":64185272,"end":64204543,"strand":1,"description":"stress induced phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:11387]"}, {"versioned_ensembl_gene_id":"ENSG00000275614.1","gene_symbol":"AL627230.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67714723,"end":67714914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277208.1","gene_symbol":"AL627230.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67713910,"end":67713967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000039600.10","gene_symbol":"SOX30","gene_name":"SRY-box 30 [Source:HGNC Symbol;Acc:HGNC:30635]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11063","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein acts as a transcriptional regulator when present in a complex with other proteins. It can activate p53 transcription to promote tumor cell apoptosis in lung cancer. The protein may be involved in the differentiation of developing male germ cells. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Apr 2015]","start":157625679,"end":157671480,"strand":-1,"description":"SRY-box 30 [Source:HGNC Symbol;Acc:HGNC:30635]"}, {"versioned_ensembl_gene_id":"ENSG00000275800.1","gene_symbol":"EIF5P2","gene_name":"eukaryotic translation initiation factor 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51466]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421391","summary":null,"start":19496378,"end":19497721,"strand":-1,"description":"eukaryotic translation initiation factor 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51466]"}, {"versioned_ensembl_gene_id":"ENSG00000225051.5","gene_symbol":"HMGB3P22","gene_name":"high mobility group box 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39314]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729595","summary":null,"start":179679032,"end":179694768,"strand":1,"description":"high mobility group box 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39314]"}, {"versioned_ensembl_gene_id":"ENSG00000234640.1","gene_symbol":"AL390763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128316282,"end":128320214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265743.1","gene_symbol":"AC138207.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30964935,"end":30965500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133640.18","gene_symbol":"LRRIQ1","gene_name":"leucine rich repeats and IQ motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25708]","synonyms":"KIAA1801,FLJ12303","biotype":"protein_coding","ncbi_id":"84125","summary":null,"start":85036314,"end":85263224,"strand":1,"description":"leucine rich repeats and IQ motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25708]"}, {"versioned_ensembl_gene_id":"ENSG00000239320.1","gene_symbol":"RPS29P26","gene_name":"ribosomal protein S29 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36490]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271591","summary":null,"start":39597832,"end":39598002,"strand":1,"description":"ribosomal protein S29 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36490]"}, {"versioned_ensembl_gene_id":"ENSG00000085840.12","gene_symbol":"ORC1","gene_name":"origin recognition complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:8487]","synonyms":"PARC1,ORC1L,HSORC1","biotype":"protein_coding","ncbi_id":"4998","summary":"The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is the largest subunit of the ORC complex. While other ORC subunits are stable throughout the cell cycle, the levels of this protein vary during the cell cycle, which has been shown to be controlled by ubiquitin-mediated proteolysis after initiation of DNA replication. This protein is found to be selectively phosphorylated during mitosis. It is also reported to interact with MYST histone acetyltransferase 2 (MyST2/HBO1), a protein involved in control of transcription silencing. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":52372829,"end":52404459,"strand":-1,"description":"origin recognition complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:8487]"}, {"versioned_ensembl_gene_id":"ENSG00000233225.3","gene_symbol":"AC004987.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39833571,"end":39834718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254557.1","gene_symbol":"AC091047.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69713390,"end":69719722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113231.13","gene_symbol":"PDE8B","gene_name":"phosphodiesterase 8B [Source:HGNC Symbol;Acc:HGNC:8794]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8622","summary":"The protein encoded by this gene is a cyclic nucleotide phosphodiesterase (PDE) that catalyzes the hydrolysis of the second messenger cAMP. The encoded protein, which does not hydrolyze cGMP, is resistant to several PDE inhibitors. Defects in this gene are a cause of autosomal dominant striatal degeneration (ADSD). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]","start":77210449,"end":77429807,"strand":1,"description":"phosphodiesterase 8B [Source:HGNC Symbol;Acc:HGNC:8794]"}, {"versioned_ensembl_gene_id":"ENSG00000102547.18","gene_symbol":"CAB39L","gene_name":"calcium binding protein 39 like [Source:HGNC Symbol;Acc:HGNC:20290]","synonyms":"MO2L,FLJ12577,bA103J18.3","biotype":"protein_coding","ncbi_id":"81617","summary":null,"start":49308650,"end":49444126,"strand":-1,"description":"calcium binding protein 39 like [Source:HGNC Symbol;Acc:HGNC:20290]"}, {"versioned_ensembl_gene_id":"ENSG00000244363.3","gene_symbol":"RPL7P23","gene_name":"ribosomal protein L7 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35658]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648000","summary":null,"start":77582376,"end":77583122,"strand":1,"description":"ribosomal protein L7 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35658]"}, {"versioned_ensembl_gene_id":"ENSG00000242428.5","gene_symbol":"C3orf67-AS1","gene_name":"C3orf67 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41063]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929238","summary":null,"start":58824437,"end":59019093,"strand":1,"description":"C3orf67 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41063]"}, {"versioned_ensembl_gene_id":"ENSG00000215065.3","gene_symbol":"DUSP8P4","gene_name":"dual specificity phosphatase 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45002]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728657","summary":null,"start":47564256,"end":47566016,"strand":1,"description":"dual specificity phosphatase 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45002]"}, {"versioned_ensembl_gene_id":"ENSG00000156232.7","gene_symbol":"WHAMM","gene_name":"WAS protein homolog associated with actin, golgi membranes and microtubules [Source:HGNC Symbol;Acc:HGNC:30493]","synonyms":"WHDC1,WHAMM1,KIAA1971","biotype":"protein_coding","ncbi_id":"123720","summary":"This gene encodes a protein that plays a role in actin nucleation, Golgi membrane association and microtubule binding. The encoded protein is a nucleation-promoting factor that regulates the Actin-related protein 2/3 complex. The activated complex initiates growth of new actin filaments by binding to existing actin filaments. The encoded protein also functions in regulation of transport from the endoplasmic reticulum to the Golgi complex and in maintenance of the Golgi complex near the centrosome. Four pseudogenes of this gene are present on the same arm of chromosome 15 as this gene. [provided by RefSeq, Aug 2013]","start":82809628,"end":82836108,"strand":1,"description":"WAS protein homolog associated with actin, golgi membranes and microtubules [Source:HGNC Symbol;Acc:HGNC:30493]"}, {"versioned_ensembl_gene_id":"ENSG00000228275.1","gene_symbol":"ARMCX3-AS1","gene_name":"ARMCX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41038]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128574","summary":null,"start":101622983,"end":101624164,"strand":-1,"description":"ARMCX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41038]"}, {"versioned_ensembl_gene_id":"ENSG00000102401.19","gene_symbol":"ARMCX3","gene_name":"armadillo repeat containing, X-linked 3 [Source:HGNC Symbol;Acc:HGNC:24065]","synonyms":"GASP6,ALEX3","biotype":"protein_coding","ncbi_id":"51566","summary":"This gene encodes a member of the ALEX family of proteins which may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and a single Armadillo (arm) repeat. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members on the X chromosome. Three transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":101622797,"end":101627843,"strand":1,"description":"armadillo repeat containing, X-linked 3 [Source:HGNC Symbol;Acc:HGNC:24065]"}, {"versioned_ensembl_gene_id":"ENSG00000108528.13","gene_symbol":"SLC25A11","gene_name":"solute carrier family 25 member 11 [Source:HGNC Symbol;Acc:HGNC:10981]","synonyms":"SLC20A4,OGC","biotype":"protein_coding","ncbi_id":"8402","summary":"The oxoglutarate/malate carrier transports 2-oxoglutarate across the inner membranes of mitochondria in an electroneutral exchange for malate or other dicarboxylic acids (summary by Iacobazzi et al., 1992 [PubMed 1457818]).[supplied by OMIM, Jan 2011]","start":4937130,"end":4940251,"strand":-1,"description":"solute carrier family 25 member 11 [Source:HGNC Symbol;Acc:HGNC:10981]"}, {"versioned_ensembl_gene_id":"ENSG00000271766.1","gene_symbol":"AC010424.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127478295,"end":127478737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250075.5","gene_symbol":"AC104806.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67417305,"end":67468251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254940.1","gene_symbol":"OR4A19P","gene_name":"olfactory receptor family 4 subfamily A member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15156]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81324","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49920312,"end":49921414,"strand":-1,"description":"olfactory receptor family 4 subfamily A member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15156]"}, {"versioned_ensembl_gene_id":"ENSG00000227816.4","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32884481,"end":32893250,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000236562.4","gene_symbol":"AC116049.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66094142,"end":66094526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241612.1","gene_symbol":"AC114728.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19813749,"end":19814231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108785.7","gene_symbol":"HSD17B1P1","gene_name":"hydroxysteroid 17-beta dehydrogenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5216]","synonyms":"SDR28C1P1,HSD17BP1,EDHB17,EDH17B1","biotype":"unprocessed_pseudogene","ncbi_id":"643646","summary":null,"start":42546764,"end":42548706,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5216]"}, {"versioned_ensembl_gene_id":"ENSG00000138472.10","gene_symbol":"GUCA1C","gene_name":"guanylate cyclase activator 1C [Source:HGNC Symbol;Acc:HGNC:4680]","synonyms":"GCAP3","biotype":"protein_coding","ncbi_id":"9626","summary":null,"start":108907792,"end":108953895,"strand":-1,"description":"guanylate cyclase activator 1C [Source:HGNC Symbol;Acc:HGNC:4680]"}, {"versioned_ensembl_gene_id":"ENSG00000239649.3","gene_symbol":"MYADML","gene_name":"myeloid associated differentiation marker like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31019]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"151325","summary":null,"start":33722721,"end":33728207,"strand":-1,"description":"myeloid associated differentiation marker like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31019]"}, {"versioned_ensembl_gene_id":"ENSG00000111012.9","gene_symbol":"CYP27B1","gene_name":"cytochrome P450 family 27 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2606]","synonyms":"VDD1,PDDR,P450c1,CYP1","biotype":"protein_coding","ncbi_id":"1594","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The protein encoded by this gene localizes to the inner mitochondrial membrane where it hydroxylates 25-hydroxyvitamin D3 at the 1alpha position. This reaction synthesizes 1alpha,25-dihydroxyvitamin D3, the active form of vitamin D3, which binds to the vitamin D receptor and regulates calcium metabolism. Thus this enzyme regulates the level of biologically active vitamin D and plays an important role in calcium homeostasis. Mutations in this gene can result in vitamin D-dependent rickets type I. [provided by RefSeq, Jul 2008]","start":57762334,"end":57768986,"strand":-1,"description":"cytochrome P450 family 27 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2606]"}, {"versioned_ensembl_gene_id":"ENSG00000204780.5","gene_symbol":"IGKV1OR9-1","gene_name":"immunoglobulin kappa variable 1/OR9-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49473]","synonyms":"IGKV1/OR9-1","biotype":"IG_V_pseudogene","ncbi_id":"103352540","summary":null,"start":65250543,"end":65250826,"strand":-1,"description":"immunoglobulin kappa variable 1/OR9-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49473]"}, {"versioned_ensembl_gene_id":"ENSG00000251139.2","gene_symbol":"AC084871.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":184813619,"end":184821300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228361.2","gene_symbol":"AL606970.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168229732,"end":168240715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235410.1","gene_symbol":"AL157896.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14074284,"end":14087605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237987.1","gene_symbol":"AL606970.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168225279,"end":168226517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258513.1","gene_symbol":"AC006349.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":74192589,"end":74192823,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249094.2","gene_symbol":"AC007834.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109880676,"end":109888467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266929.1","gene_symbol":"AC067852.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":42536510,"end":42562062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272707.1","gene_symbol":"AC046143.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194637505,"end":194637664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280711.1","gene_symbol":"AC108024.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128768228,"end":128769948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128524.4","gene_symbol":"ATP6V1F","gene_name":"ATPase H+ transporting V1 subunit F [Source:HGNC Symbol;Acc:HGNC:16832]","synonyms":"Vma7,VATF,ATP6S14","biotype":"protein_coding","ncbi_id":"9296","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is the V1 domain F subunit protein. [provided by RefSeq, Jul 2008]","start":128862826,"end":128865844,"strand":1,"description":"ATPase H+ transporting V1 subunit F [Source:HGNC Symbol;Acc:HGNC:16832]"}, {"versioned_ensembl_gene_id":"ENSG00000248479.1","gene_symbol":"AC104137.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65702202,"end":65705553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236618.2","gene_symbol":"PITPNA-AS1","gene_name":"PITPNA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44116]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100306951","summary":null,"start":1516931,"end":1518096,"strand":1,"description":"PITPNA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44116]"}, {"versioned_ensembl_gene_id":"ENSG00000232881.2","gene_symbol":"RPS10P21","gene_name":"ribosomal protein S10 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35906]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271351","summary":null,"start":71913704,"end":71914178,"strand":-1,"description":"ribosomal protein S10 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35906]"}, {"versioned_ensembl_gene_id":"ENSG00000100519.11","gene_symbol":"PSMC6","gene_name":"proteasome 26S subunit, ATPase 6 [Source:HGNC Symbol;Acc:HGNC:9553]","synonyms":"p42","biotype":"protein_coding","ncbi_id":"5706","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. Pseudogenes have been identified on chromosomes 8 and 12. [provided by RefSeq, Jul 2008]","start":52707172,"end":52728587,"strand":1,"description":"proteasome 26S subunit, ATPase 6 [Source:HGNC Symbol;Acc:HGNC:9553]"}, {"versioned_ensembl_gene_id":"ENSG00000244945.1","gene_symbol":"AC136604.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179595904,"end":179603741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226349.1","gene_symbol":"AC099066.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":225710968,"end":225736274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266934.1","gene_symbol":"AC005746.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":61382785,"end":61384680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120149.8","gene_symbol":"MSX2","gene_name":"msh homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7392]","synonyms":"PFM1,PFM,MSH,HOX8,FPP,CRS2","biotype":"protein_coding","ncbi_id":"4488","summary":"This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2. [provided by RefSeq, Jul 2008]","start":174724533,"end":174730893,"strand":1,"description":"msh homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7392]"}, {"versioned_ensembl_gene_id":"ENSG00000233541.4","gene_symbol":"AP000926.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123051161,"end":123051401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235413.3","gene_symbol":"KRT18P63","gene_name":"keratin 18 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:48890]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288868","summary":null,"start":17911674,"end":17912976,"strand":1,"description":"keratin 18 pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:48890]"}, {"versioned_ensembl_gene_id":"ENSG00000253244.1","gene_symbol":"AC113423.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174056060,"end":174056585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255214.1","gene_symbol":"AP006587.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49871826,"end":49874067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188909.4","gene_symbol":"BSX","gene_name":"brain specific homeobox [Source:HGNC Symbol;Acc:HGNC:20450]","synonyms":"BSX1","biotype":"protein_coding","ncbi_id":"390259","summary":null,"start":122977570,"end":122981720,"strand":-1,"description":"brain specific homeobox [Source:HGNC Symbol;Acc:HGNC:20450]"}, {"versioned_ensembl_gene_id":"ENSG00000128591.15","gene_symbol":"FLNC","gene_name":"filamin C [Source:HGNC Symbol;Acc:HGNC:3756]","synonyms":"FLN2,ABPL,ABP-280","biotype":"protein_coding","ncbi_id":"2318","summary":"This gene encodes one of three related filamin genes, specifically gamma filamin. These filamin proteins crosslink actin filaments into orthogonal networks in cortical cytoplasm and participate in the anchoring of membrane proteins for the actin cytoskeleton. Three functional domains exist in filamin: an N-terminal filamentous actin-binding domain, a C-terminal self-association domain, and a membrane glycoprotein-binding domain. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":128830377,"end":128859274,"strand":1,"description":"filamin C [Source:HGNC Symbol;Acc:HGNC:3756]"}, {"versioned_ensembl_gene_id":"ENSG00000148362.10","gene_symbol":"PAXX","gene_name":"PAXX, non-homologous end joining factor [Source:HGNC Symbol;Acc:HGNC:27849]","synonyms":"XLS,C9orf142","biotype":"protein_coding","ncbi_id":"286257","summary":"The protein encoded by this gene plays a role in the nonhomologous end joining (NHEJ) pathway of DNA double-strand break repair. The encoded protein may function to stabilize the Ku70/Ku80 heterodimer to facilitate the assembly and maintain the stability of the NHEJ complex. [provided by RefSeq, Jul 2016]","start":136992418,"end":136993984,"strand":1,"description":"PAXX, non-homologous end joining factor [Source:HGNC Symbol;Acc:HGNC:27849]"}, {"versioned_ensembl_gene_id":"ENSG00000109805.9","gene_symbol":"NCAPG","gene_name":"non-SMC condensin I complex subunit G [Source:HGNC Symbol;Acc:HGNC:24304]","synonyms":"CAP-G,YCG1,hCAP-G,FLJ12450","biotype":"protein_coding","ncbi_id":"64151","summary":"This gene encodes a subunit of the condensin complex, which is responsible for the condensation and stabilization of chromosomes during mitosis and meiosis. Phosphorylation of the encoded protein activates the condensin complex. There are pseudogenes for this gene on chromosomes 8 and 15. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":17810902,"end":17844862,"strand":1,"description":"non-SMC condensin I complex subunit G [Source:HGNC Symbol;Acc:HGNC:24304]"}, {"versioned_ensembl_gene_id":"ENSG00000276957.1","gene_symbol":"AL158063.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102593338,"end":102593873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276715.4","gene_symbol":"YWHAEP7","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49437]","synonyms":"LOC284100","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284100","summary":null,"start":37828305,"end":37884743,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49437]"}, {"versioned_ensembl_gene_id":"ENSG00000279288.1","gene_symbol":"AC073346.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":113075124,"end":113077181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124232.10","gene_symbol":"RBPJL","gene_name":"recombination signal binding protein for immunoglobulin kappa J region like [Source:HGNC Symbol;Acc:HGNC:13761]","synonyms":"SUHL,SUH,RBPSUHL,RBP-L","biotype":"protein_coding","ncbi_id":"11317","summary":"This gene encodes a member of the suppressor of hairless protein family. A similar protein in mouse is a transcription factor that binds to DNA sequences almost identical to that bound by the Notch receptor signaling pathway transcription factor recombining binding protein J. The mouse protein has been shown to activate transcription in concert with Epstein-Barr virus nuclear antigen-2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":45306851,"end":45317824,"strand":1,"description":"recombination signal binding protein for immunoglobulin kappa J region like [Source:HGNC Symbol;Acc:HGNC:13761]"}, {"versioned_ensembl_gene_id":"ENSG00000226109.1","gene_symbol":"CR382333.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29931024,"end":29932015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265630.2","gene_symbol":"GLUD1P8","gene_name":"glutamate dehydrogenase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23637]","synonyms":"GLUDP8,bA144G6.5","biotype":"unprocessed_pseudogene","ncbi_id":"414213","summary":null,"start":47563604,"end":47569697,"strand":1,"description":"glutamate dehydrogenase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23637]"}, {"versioned_ensembl_gene_id":"ENSG00000184611.11","gene_symbol":"KCNH7","gene_name":"potassium voltage-gated channel subfamily H member 7 [Source:HGNC Symbol;Acc:HGNC:18863]","synonyms":"Kv11.3,HERG3,erg3","biotype":"protein_coding","ncbi_id":"90134","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. There are at least two alternatively spliced transcript variants derived from this gene and encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":162371407,"end":162838730,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 7 [Source:HGNC Symbol;Acc:HGNC:18863]"}, {"versioned_ensembl_gene_id":"ENSG00000162620.15","gene_symbol":"LRRIQ3","gene_name":"leucine rich repeats and IQ motif containing 3 [Source:HGNC Symbol;Acc:HGNC:28318]","synonyms":"MGC22773,LRRC44","biotype":"protein_coding","ncbi_id":"127255","summary":null,"start":74026015,"end":74198187,"strand":-1,"description":"leucine rich repeats and IQ motif containing 3 [Source:HGNC Symbol;Acc:HGNC:28318]"}, {"versioned_ensembl_gene_id":"ENSG00000228079.2","gene_symbol":"AC012368.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64086353,"end":64088246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115271.10","gene_symbol":"GCA","gene_name":"grancalcin [Source:HGNC Symbol;Acc:HGNC:15990]","synonyms":"GCL","biotype":"protein_coding","ncbi_id":"25801","summary":"This gene encodes a calcium-binding protein that is abundant in neutrophils and macrophages. In the absence of divalent cation, this protein localizes to the cytosolic fraction; with magnesium alone, it partitions with the granule fraction; and in the presence of magnesium and calcium, it associates with both the granule and membrane fractions. Alternative splicing and use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":162318840,"end":162371595,"strand":1,"description":"grancalcin [Source:HGNC Symbol;Acc:HGNC:15990]"}, {"versioned_ensembl_gene_id":"ENSG00000137478.14","gene_symbol":"FCHSD2","gene_name":"FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:HGNC:29114]","synonyms":"KIAA0769,SH3MD3","biotype":"protein_coding","ncbi_id":"9873","summary":null,"start":72836745,"end":73142261,"strand":-1,"description":"FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:HGNC:29114]"}, {"versioned_ensembl_gene_id":"ENSG00000181754.6","gene_symbol":"AMIGO1","gene_name":"adhesion molecule with Ig like domain 1 [Source:HGNC Symbol;Acc:HGNC:20824]","synonyms":"KIAA1163,AMIGO","biotype":"protein_coding","ncbi_id":"57463","summary":null,"start":109504175,"end":109509738,"strand":-1,"description":"adhesion molecule with Ig like domain 1 [Source:HGNC Symbol;Acc:HGNC:20824]"}, {"versioned_ensembl_gene_id":"ENSG00000279013.1","gene_symbol":"AC110774.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91603275,"end":91605292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275410.4","gene_symbol":"HNF1B","gene_name":"HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]","synonyms":"VHNF1,TCF2,MODY5,LFB3,HNF1beta","biotype":"protein_coding","ncbi_id":"6928","summary":"This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":37686432,"end":37745247,"strand":-1,"description":"HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]"}, {"versioned_ensembl_gene_id":"ENSG00000203711.11","gene_symbol":"C6orf99","gene_name":"chromosome 6 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:21179]","synonyms":"yR211F11.1","biotype":"lincRNA","ncbi_id":"100130967","summary":null,"start":158869939,"end":158910353,"strand":1,"description":"chromosome 6 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:21179]"}, {"versioned_ensembl_gene_id":"ENSG00000257000.1","gene_symbol":"AC137590.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132077803,"end":132080460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249785.1","gene_symbol":"LINC02103","gene_name":"long intergenic non-protein coding RNA 2103 [Source:HGNC Symbol;Acc:HGNC:52958]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374698","summary":null,"start":28286389,"end":28287665,"strand":-1,"description":"long intergenic non-protein coding RNA 2103 [Source:HGNC Symbol;Acc:HGNC:52958]"}, {"versioned_ensembl_gene_id":"ENSG00000280281.1","gene_symbol":"AL049781.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32879246,"end":32882830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258561.1","gene_symbol":"AL359232.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66212810,"end":66509394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237009.2","gene_symbol":"GLIS3-AS1","gene_name":"GLIS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28260]","synonyms":"MGC16153,C9orf70","biotype":"antisense_RNA","ncbi_id":"84850","summary":null,"start":3898642,"end":3901248,"strand":1,"description":"GLIS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28260]"}, {"versioned_ensembl_gene_id":"ENSG00000258490.1","gene_symbol":"AL049835.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66969038,"end":66969816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187475.5","gene_symbol":"HIST1H1T","gene_name":"histone cluster 1 H1 family member t [Source:HGNC Symbol;Acc:HGNC:4720]","synonyms":"H1t,H1FT","biotype":"protein_coding","ncbi_id":"3010","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26107419,"end":26108136,"strand":-1,"description":"histone cluster 1 H1 family member t [Source:HGNC Symbol;Acc:HGNC:4720]"}, {"versioned_ensembl_gene_id":"ENSG00000232935.2","gene_symbol":"AL359094.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127013501,"end":127026475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248984.1","gene_symbol":"AC004054.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91108023,"end":91112790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276116.2","gene_symbol":"FUT8-AS1","gene_name":"FUT8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44294]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"645431","summary":null,"start":65411170,"end":65412690,"strand":-1,"description":"FUT8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44294]"}, {"versioned_ensembl_gene_id":"ENSG00000275691.1","gene_symbol":"AC026461.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56676132,"end":56677763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229717.2","gene_symbol":"AC110615.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75830751,"end":75832705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197893.13","gene_symbol":"NRAP","gene_name":"nebulin related anchoring protein [Source:HGNC Symbol;Acc:HGNC:7988]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4892","summary":null,"start":113588716,"end":113664127,"strand":-1,"description":"nebulin related anchoring protein [Source:HGNC Symbol;Acc:HGNC:7988]"}, {"versioned_ensembl_gene_id":"ENSG00000258170.1","gene_symbol":"AC089998.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82481118,"end":82497560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146676.8","gene_symbol":"PURB","gene_name":"purine rich element binding protein B [Source:HGNC Symbol;Acc:HGNC:9702]","synonyms":"PURBETA","biotype":"protein_coding","ncbi_id":"5814","summary":"This gene product is a sequence-specific, single-stranded DNA-binding protein. It binds preferentially to the single strand of the purine-rich element termed PUR, which is present at origins of replication and in gene flanking regions in a variety of eukaryotes from yeasts through humans. Thus, it is implicated in the control of both DNA replication and transcription. Deletion of this gene has been associated with myelodysplastic syndrome and acute myelogenous leukemia. [provided by RefSeq, Jul 2008]","start":44876293,"end":44885361,"strand":-1,"description":"purine rich element binding protein B [Source:HGNC Symbol;Acc:HGNC:9702]"}, {"versioned_ensembl_gene_id":"ENSG00000272768.1","gene_symbol":"AC004854.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44884953,"end":44886393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225470.7","gene_symbol":"JPX","gene_name":"JPX transcript, XIST activator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37191]","synonyms":"NCRNA00183,LINC00183,ENOX,DCBALD06","biotype":"lincRNA","ncbi_id":"554203","summary":"JPX is a nonprotein-coding RNA transcribed from a gene within the X-inactivation center (XIC; MIM 314670) that appears to participate in X chromosome inactivation (Tian et al., 2010 [PubMed 21029862]).[supplied by OMIM, Feb 2011]","start":73944184,"end":74070408,"strand":1,"description":"JPX transcript, XIST activator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37191]"}, {"versioned_ensembl_gene_id":"ENSG00000282634.1","gene_symbol":"AC243301.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":384081,"end":390528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274267.1","gene_symbol":"HIST1H3B","gene_name":"histone cluster 1 H3 family member b [Source:HGNC Symbol;Acc:HGNC:4776]","synonyms":"H3FL,H3/l","biotype":"protein_coding","ncbi_id":"8358","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26031650,"end":26032060,"strand":-1,"description":"histone cluster 1 H3 family member b [Source:HGNC Symbol;Acc:HGNC:4776]"}, {"versioned_ensembl_gene_id":"ENSG00000232127.2","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31131271,"end":31133087,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000108443.13","gene_symbol":"RPS6KB1","gene_name":"ribosomal protein S6 kinase B1 [Source:HGNC Symbol;Acc:HGNC:10436]","synonyms":"p70(S6K)-alpha,STK14A,S6K1,PS6K","biotype":"protein_coding","ncbi_id":"6198","summary":"This gene encodes a member of the ribosomal S6 kinase family of serine/threonine kinases. The encoded protein responds to mTOR (mammalian target of rapamycin) signaling to promote protein synthesis, cell growth, and cell proliferation. Activity of this gene has been associated with human cancer. Alternatively spliced transcript variants have been observed. The use of alternative translation start sites results in isoforms with longer or shorter N-termini which may differ in their subcellular localizations. There are two pseudogenes for this gene on chromosome 17. [provided by RefSeq, Jan 2013]","start":59893046,"end":59950564,"strand":1,"description":"ribosomal protein S6 kinase B1 [Source:HGNC Symbol;Acc:HGNC:10436]"}, {"versioned_ensembl_gene_id":"ENSG00000240680.1","gene_symbol":"AC016831.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130823205,"end":130823511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146859.6","gene_symbol":"TMEM140","gene_name":"transmembrane protein 140 [Source:HGNC Symbol;Acc:HGNC:21870]","synonyms":"FLJ11000","biotype":"protein_coding","ncbi_id":"55281","summary":null,"start":135148072,"end":135166215,"strand":1,"description":"transmembrane protein 140 [Source:HGNC Symbol;Acc:HGNC:21870]"}, {"versioned_ensembl_gene_id":"ENSG00000172568.4","gene_symbol":"FNDC9","gene_name":"fibronectin type III domain containing 9 [Source:HGNC Symbol;Acc:HGNC:33547]","synonyms":"MGC27121,C5orf40","biotype":"protein_coding","ncbi_id":"408263","summary":null,"start":157341600,"end":157345721,"strand":-1,"description":"fibronectin type III domain containing 9 [Source:HGNC Symbol;Acc:HGNC:33547]"}, {"versioned_ensembl_gene_id":"ENSG00000170439.6","gene_symbol":"METTL7B","gene_name":"methyltransferase like 7B [Source:HGNC Symbol;Acc:HGNC:28276]","synonyms":"MGC17301,ALDI","biotype":"protein_coding","ncbi_id":"196410","summary":null,"start":55681546,"end":55684611,"strand":1,"description":"methyltransferase like 7B [Source:HGNC Symbol;Acc:HGNC:28276]"}, {"versioned_ensembl_gene_id":"ENSG00000090889.11","gene_symbol":"KIF4A","gene_name":"kinesin family member 4A [Source:HGNC Symbol;Acc:HGNC:13339]","synonyms":"MRX100,KIF4-G1,KIF4,HSA271784,FLJ20631,FLJ14204,FLJ12655,FLJ12530","biotype":"protein_coding","ncbi_id":"24137","summary":"This gene encodes a member of the kinesin 4 subfamily of kinesin related proteins. The encoded protein is an ATP dependent microtubule-based motor protein that is involved in the intracellular transport of membranous organelles. This protein also associates with condensed chromosome arms and may be involved in maintaining chromosome integrity during mitosis. This protein may also be involved in the organization of the central spindle prior to cytokinesis. A pseudogene of this gene is found on chromosome X.[provided by RefSeq, Mar 2010]","start":70290090,"end":70420832,"strand":1,"description":"kinesin family member 4A [Source:HGNC Symbol;Acc:HGNC:13339]"}, {"versioned_ensembl_gene_id":"ENSG00000231053.1","gene_symbol":"AL357752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70361486,"end":70362374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135439.11","gene_symbol":"AGAP2","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:16921]","synonyms":"CENTG1","biotype":"protein_coding","ncbi_id":"116986","summary":"The protein encoded by this gene belongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor by activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, and promotes cancer cell invasion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":57723761,"end":57742157,"strand":-1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:16921]"}, {"versioned_ensembl_gene_id":"ENSG00000205325.1","gene_symbol":"AC005863.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14767583,"end":14780203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172324.5","gene_symbol":"OR5A2","gene_name":"olfactory receptor family 5 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15249]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219981","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59416969,"end":59426412,"strand":-1,"description":"olfactory receptor family 5 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15249]"}, {"versioned_ensembl_gene_id":"ENSG00000095574.11","gene_symbol":"IKZF5","gene_name":"IKAROS family zinc finger 5 [Source:HGNC Symbol;Acc:HGNC:14283]","synonyms":"ZNFN1A5,Pegasus,FLJ22973","biotype":"protein_coding","ncbi_id":"64376","summary":"Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Pegasus, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002]","start":122990806,"end":123008817,"strand":-1,"description":"IKAROS family zinc finger 5 [Source:HGNC Symbol;Acc:HGNC:14283]"}, {"versioned_ensembl_gene_id":"ENSG00000255858.1","gene_symbol":"AC055720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26315715,"end":26317813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228522.2","gene_symbol":"AL845321.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63330326,"end":63343660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226834.1","gene_symbol":"BX248310.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31301504,"end":31302238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223510.6","gene_symbol":"CDRT15","gene_name":"CMT1A duplicated region transcript 15 [Source:HGNC Symbol;Acc:HGNC:14395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146822","summary":null,"start":14235673,"end":14236862,"strand":-1,"description":"CMT1A duplicated region transcript 15 [Source:HGNC Symbol;Acc:HGNC:14395]"}, {"versioned_ensembl_gene_id":"ENSG00000239605.9","gene_symbol":"STPG4","gene_name":"sperm-tail PG-rich repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26850]","synonyms":"FLJ40172,C2orf61,C2orf61","biotype":"protein_coding","ncbi_id":"285051","summary":null,"start":47045538,"end":47155287,"strand":-1,"description":"sperm-tail PG-rich repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:26850]"}, {"versioned_ensembl_gene_id":"ENSG00000236722.1","gene_symbol":"AC116036.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58511310,"end":58511676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084110.10","gene_symbol":"HAL","gene_name":"histidine ammonia-lyase [Source:HGNC Symbol;Acc:HGNC:4806]","synonyms":"HIS","biotype":"protein_coding","ncbi_id":"3034","summary":"Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":95972662,"end":95996365,"strand":-1,"description":"histidine ammonia-lyase [Source:HGNC Symbol;Acc:HGNC:4806]"}, {"versioned_ensembl_gene_id":"ENSG00000232349.2","gene_symbol":"YBX1P7","gene_name":"Y-box binding protein 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861431","summary":null,"start":132488554,"end":132489088,"strand":-1,"description":"Y-box binding protein 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42428]"}, {"versioned_ensembl_gene_id":"ENSG00000205420.10","gene_symbol":"KRT6A","gene_name":"keratin 6A [Source:HGNC Symbol;Acc:HGNC:6443]","synonyms":"KRT6D,KRT6C,K6D,K6C,CK6D,CK6C","biotype":"protein_coding","ncbi_id":"3853","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. As many as six of this type II cytokeratin (KRT6) have been identified; the multiplicity of the genes is attributed to successive gene duplication events. The genes are expressed with family members KRT16 and/or KRT17 in the filiform papillae of the tongue, the stratified epithelial lining of oral mucosa and esophagus, the outer root sheath of hair follicles, and the glandular epithelia. This KRT6 gene in particular encodes the most abundant isoform. Mutations in these genes have been associated with pachyonychia congenita. In addition, peptides from the C-terminal region of the protein have antimicrobial activity against bacterial pathogens. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Oct 2014]","start":52487174,"end":52493257,"strand":-1,"description":"keratin 6A [Source:HGNC Symbol;Acc:HGNC:6443]"}, {"versioned_ensembl_gene_id":"ENSG00000237125.8","gene_symbol":"HAND2-AS1","gene_name":"HAND2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48872]","synonyms":"NBLA00301,FLJ11539,DEIN","biotype":"antisense_RNA","ncbi_id":"79804","summary":null,"start":173527270,"end":173591324,"strand":1,"description":"HAND2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48872]"}, {"versioned_ensembl_gene_id":"ENSG00000172831.11","gene_symbol":"CES2","gene_name":"carboxylesterase 2 [Source:HGNC Symbol;Acc:HGNC:1864]","synonyms":"CE-2,iCE,CES2A1","biotype":"protein_coding","ncbi_id":"8824","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. The protein encoded by this gene is the major intestinal enzyme and functions in intestine drug clearance. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2010]","start":66934444,"end":66945096,"strand":1,"description":"carboxylesterase 2 [Source:HGNC Symbol;Acc:HGNC:1864]"}, {"versioned_ensembl_gene_id":"ENSG00000011052.21","gene_symbol":"NME1-NME2","gene_name":"NME1-NME2 readthrough [Source:HGNC Symbol;Acc:HGNC:33531]","synonyms":"NMELV,NM23-LV","biotype":"protein_coding","ncbi_id":"654364","summary":"This locus represents naturally occurring read-through transcription between the neighboring NME1 and NME2 genes. The significance of this read-through transcription and the function of the resulting protein product have not yet been determined. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":51153590,"end":51171744,"strand":1,"description":"NME1-NME2 readthrough [Source:HGNC Symbol;Acc:HGNC:33531]"}, {"versioned_ensembl_gene_id":"ENSG00000168301.12","gene_symbol":"KCTD6","gene_name":"potassium channel tetramerization domain containing 6 [Source:HGNC Symbol;Acc:HGNC:22235]","synonyms":"MGC27385,KCASH3","biotype":"protein_coding","ncbi_id":"200845","summary":null,"start":58492114,"end":58502360,"strand":1,"description":"potassium channel tetramerization domain containing 6 [Source:HGNC Symbol;Acc:HGNC:22235]"}, {"versioned_ensembl_gene_id":"ENSG00000185842.15","gene_symbol":"DNAH14","gene_name":"dynein axonemal heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:2945]","synonyms":"Dnahc14,DKFZp781B1548,C1orf67,MGC27277,HL18,HL-18","biotype":"protein_coding","ncbi_id":"127602","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. Two major classes of dyneins, axonemal and cytoplasmic, have been identified. DNAH14 is an axonemal dynein heavy chain (DHC) (Vaughan et al., 1996 [PubMed 8812413]).[supplied by OMIM, Mar 2008]","start":224896262,"end":225399292,"strand":1,"description":"dynein axonemal heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:2945]"}, {"versioned_ensembl_gene_id":"ENSG00000111912.19","gene_symbol":"NCOA7","gene_name":"nuclear receptor coactivator 7 [Source:HGNC Symbol;Acc:HGNC:21081]","synonyms":"TLDC4,ERAP140,dJ187J11.3","biotype":"protein_coding","ncbi_id":"135112","summary":null,"start":125781161,"end":125932030,"strand":1,"description":"nuclear receptor coactivator 7 [Source:HGNC Symbol;Acc:HGNC:21081]"}, {"versioned_ensembl_gene_id":"ENSG00000175121.11","gene_symbol":"WFDC5","gene_name":"WAP four-disulfide core domain 5 [Source:HGNC Symbol;Acc:HGNC:20477]","synonyms":"WAP1,dJ211D12.5","biotype":"protein_coding","ncbi_id":"149708","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. Most WFDC proteins contain only one WFDC domain, and this encoded protein contains two WFDC domains. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. [provided by RefSeq, Jul 2008]","start":45109452,"end":45115172,"strand":-1,"description":"WAP four-disulfide core domain 5 [Source:HGNC Symbol;Acc:HGNC:20477]"}, {"versioned_ensembl_gene_id":"ENSG00000125384.6","gene_symbol":"PTGER2","gene_name":"prostaglandin E receptor 2 [Source:HGNC Symbol;Acc:HGNC:9594]","synonyms":"EP2","biotype":"protein_coding","ncbi_id":"5732","summary":"This gene encodes a receptor for prostaglandin E2, a metabolite of arachidonic acid which has different biologic activities in a wide range of tissues. Mutations in this gene are associated with aspirin-induced susceptibility to asthma. [provided by RefSeq, Oct 2009]","start":52314305,"end":52328606,"strand":1,"description":"prostaglandin E receptor 2 [Source:HGNC Symbol;Acc:HGNC:9594]"}, {"versioned_ensembl_gene_id":"ENSG00000257609.1","gene_symbol":"AC091515.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81868368,"end":81869046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236088.9","gene_symbol":"COX10-AS1","gene_name":"COX10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38873]","synonyms":"COX10AS,COX10-AS","biotype":"processed_transcript","ncbi_id":"100874058","summary":null,"start":13756478,"end":14069495,"strand":-1,"description":"COX10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38873]"}, {"versioned_ensembl_gene_id":"ENSG00000281604.1","gene_symbol":"AC020679.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21514120,"end":21566989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204758.7","gene_symbol":"AC008429.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":172954786,"end":172959392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254295.1","gene_symbol":"AC008429.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":172954907,"end":172957162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240338.5","gene_symbol":"AC009078.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75226074,"end":75228197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260977.1","gene_symbol":"AC016722.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46777783,"end":46780245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000016402.13","gene_symbol":"IL20RA","gene_name":"interleukin 20 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6003]","synonyms":"ZCYTOR7,IL-20R1","biotype":"protein_coding","ncbi_id":"53832","summary":"This gene encodes a member of the type II cytokine receptor family. The encoded protein is a subunit of the receptor for interleukin 20, a cytokine that may be involved in epidermal function. The interleukin 20 receptor is a heterodimeric complex consisting of the encoded protein and interleukin 20 receptor beta. This gene and interleukin 20 receptor beta are highly expressed in skin, and are upregulated in psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":136999971,"end":137045180,"strand":-1,"description":"interleukin 20 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6003]"}, {"versioned_ensembl_gene_id":"ENSG00000262265.1","gene_symbol":"AC002558.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47161075,"end":47162064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216904.2","gene_symbol":"SOCS5P5","gene_name":"suppressor of cytokine signaling 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44601]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643884","summary":null,"start":113222166,"end":113224072,"strand":1,"description":"suppressor of cytokine signaling 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44601]"}, {"versioned_ensembl_gene_id":"ENSG00000226970.2","gene_symbol":"AL450063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84244334,"end":84244577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270549.1","gene_symbol":"AL451044.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62530636,"end":62530873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251399.1","gene_symbol":"AC092542.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79596542,"end":79597173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281334.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000277695.1","gene_symbol":"AC097478.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89747802,"end":89755853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274238.1","gene_symbol":"AC097478.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89743792,"end":89744305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155868.7","gene_symbol":"MED7","gene_name":"mediator complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:2378]","synonyms":"CRSP9,CRSP33","biotype":"protein_coding","ncbi_id":"9443","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":157137412,"end":157159019,"strand":-1,"description":"mediator complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:2378]"}, {"versioned_ensembl_gene_id":"ENSG00000117280.12","gene_symbol":"RAB29","gene_name":"RAB29, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9789]","synonyms":"RAB7L1,RAB7L","biotype":"protein_coding","ncbi_id":"8934","summary":null,"start":205767986,"end":205775460,"strand":-1,"description":"RAB29, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9789]"}, {"versioned_ensembl_gene_id":"ENSG00000168928.12","gene_symbol":"CTRB2","gene_name":"chymotrypsinogen B2 [Source:HGNC Symbol;Acc:HGNC:2522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440387","summary":"This gene encodes a member of the serine protease family of enzymes and forms a principal precursor of the pancreatic proteolytic enzymes. The encoded preproprotein is synthesized in the acinar cells of the pancreas and secreted into the small intestine where it undergoes proteolytic activation to generate a functional enzyme. This CTRB2 gene is located head-to-head with the related CTRB1 gene. Some human populations have an alternate haplotype which inverts a 16.6 Kb region containing portions of intron 1, exon 1, and the upstream sequence of the CTRB1 and CTRB2 genes. In this inversion haplotype exon 1 and flanking sequence is swapped in CTRB1 and CTRB2. This inversion is associated with differential gene expression and increased risk for chronic pancreatitis. The GRCh38 assembly represents the minor allele for SNP rs8048956 of the CTRB1 gene. SNP rs8048956 is diagnostic for this inversion. [provided by RefSeq, Jan 2021]","start":75204096,"end":75207185,"strand":-1,"description":"chymotrypsinogen B2 [Source:HGNC Symbol;Acc:HGNC:2522]"}, {"versioned_ensembl_gene_id":"ENSG00000219773.1","gene_symbol":"RPSAP45","gene_name":"ribosomal protein SA pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35857]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728562","summary":null,"start":112355841,"end":112356714,"strand":-1,"description":"ribosomal protein SA pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35857]"}, {"versioned_ensembl_gene_id":"ENSG00000197629.5","gene_symbol":"MPEG1","gene_name":"macrophage expressed 1 [Source:HGNC Symbol;Acc:HGNC:29619]","synonyms":"MPG1","biotype":"protein_coding","ncbi_id":"219972","summary":null,"start":59208510,"end":59212951,"strand":-1,"description":"macrophage expressed 1 [Source:HGNC Symbol;Acc:HGNC:29619]"}, {"versioned_ensembl_gene_id":"ENSG00000110042.7","gene_symbol":"DTX4","gene_name":"deltex E3 ubiquitin ligase 4 [Source:HGNC Symbol;Acc:HGNC:29151]","synonyms":"RNF155,KIAA0937","biotype":"protein_coding","ncbi_id":"23220","summary":null,"start":59171430,"end":59208587,"strand":1,"description":"deltex E3 ubiquitin ligase 4 [Source:HGNC Symbol;Acc:HGNC:29151]"}, {"versioned_ensembl_gene_id":"ENSG00000240674.1","gene_symbol":"AC106872.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165012366,"end":165012845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230498.1","gene_symbol":"AL035409.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77067920,"end":77078482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205331.5","gene_symbol":"OR6C72P","gene_name":"olfactory receptor family 6 subfamily C member 72 pseudogene [Source:HGNC Symbol;Acc:HGNC:31301]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403288","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55283750,"end":55284641,"strand":1,"description":"olfactory receptor family 6 subfamily C member 72 pseudogene [Source:HGNC Symbol;Acc:HGNC:31301]"}, {"versioned_ensembl_gene_id":"ENSG00000213451.2","gene_symbol":"OR6C69P","gene_name":"olfactory receptor family 6 subfamily C member 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:31298]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403285","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55262539,"end":55263431,"strand":1,"description":"olfactory receptor family 6 subfamily C member 69 pseudogene [Source:HGNC Symbol;Acc:HGNC:31298]"}, {"versioned_ensembl_gene_id":"ENSG00000227300.12","gene_symbol":"KRT16P2","gene_name":"keratin 16 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37807]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400578","summary":null,"start":16829999,"end":16832830,"strand":-1,"description":"keratin 16 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37807]"}, {"versioned_ensembl_gene_id":"ENSG00000080298.15","gene_symbol":"RFX3","gene_name":"regulatory factor X3 [Source:HGNC Symbol;Acc:HGNC:9984]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5991","summary":"This gene is a member of the regulatory factor X gene family, which encodes transcription factors that contain a highly-conserved winged helix DNA binding domain. The protein encoded by this gene is structurally related to regulatory factors X1, X2, X4, and X5. It is a transcriptional activator that can bind DNA as a monomer or as a heterodimer with other RFX family members. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]","start":3218297,"end":3526004,"strand":-1,"description":"regulatory factor X3 [Source:HGNC Symbol;Acc:HGNC:9984]"}, {"versioned_ensembl_gene_id":"ENSG00000282489.1","gene_symbol":"AC016482.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37164063,"end":37164586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130723.18","gene_symbol":"PRRC2B","gene_name":"proline rich coiled-coil 2B [Source:HGNC Symbol;Acc:HGNC:28121]","synonyms":"MGC10526,LQFBS-1,KIAA0515,BAT2L1,BAT2L","biotype":"protein_coding","ncbi_id":"84726","summary":null,"start":131394093,"end":131500197,"strand":1,"description":"proline rich coiled-coil 2B [Source:HGNC Symbol;Acc:HGNC:28121]"}, {"versioned_ensembl_gene_id":"ENSG00000220948.4","gene_symbol":"TRIM51GP","gene_name":"tripartite motif-containing 51G, pseudogene [Source:HGNC Symbol;Acc:HGNC:43972]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"120824","summary":null,"start":48975501,"end":48981695,"strand":-1,"description":"tripartite motif-containing 51G, pseudogene [Source:HGNC Symbol;Acc:HGNC:43972]"}, {"versioned_ensembl_gene_id":"ENSG00000214360.4","gene_symbol":"EFCAB9","gene_name":"EF-hand calcium binding domain 9 [Source:HGNC Symbol;Acc:HGNC:34530]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285588","summary":"This gene encodes a protein with a C-terminal EF-hand calcium-binding domain similar to that found in penta-EF-hand (PEF) protein family members. The EF-hand is a helix-loop-helix structure with a canonical twelve-residue sequence that coordinates a calcium molecule with pentagonal bipyramidal symmetry. [provided by RefSeq, Jul 2017]","start":172194172,"end":172203452,"strand":1,"description":"EF-hand calcium binding domain 9 [Source:HGNC Symbol;Acc:HGNC:34530]"}, {"versioned_ensembl_gene_id":"ENSG00000227836.1","gene_symbol":"AC008850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96942299,"end":96943184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234530.8","gene_symbol":"NFKBIL1","gene_name":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]","synonyms":"IKBL,NFKBIL","biotype":"protein_coding","ncbi_id":"4795","summary":"This gene encodes a divergent member of the I-kappa-B family of proteins. Its function has not been determined. The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":31534315,"end":31546261,"strand":1,"description":"NFKB inhibitor like 1 [Source:HGNC Symbol;Acc:HGNC:7800]"}, {"versioned_ensembl_gene_id":"ENSG00000276336.4","gene_symbol":"SCARF1","gene_name":"scavenger receptor class F member 1 [Source:HGNC Symbol;Acc:HGNC:16820]","synonyms":"SREC1,SREC,KIAA0149","biotype":"protein_coding","ncbi_id":"8578","summary":"The protein encoded by this gene is a scavenger receptor that is expressed in endothelial cells. It regulates the uptake of chemically modified low density lipoproteins, including acetylated low density lipoprotein (Ac-LDL), and it may be involved in atherogenesis. This gene is regulated by the transcription factors ZNF444/EZF-2 and SP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":1633858,"end":1645747,"strand":-1,"description":"scavenger receptor class F member 1 [Source:HGNC Symbol;Acc:HGNC:16820]"}, {"versioned_ensembl_gene_id":"ENSG00000102385.12","gene_symbol":"DRP2","gene_name":"dystrophin related protein 2 [Source:HGNC Symbol;Acc:HGNC:3032]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1821","summary":"Members of the dystrophin family of proteins perform a critical role in the maintenance of membrane-associated complexes at points of intercellular contact in vertebrate cells. The protein encoded by this gene is predicted to resemble certain short C-terminal isoforms of dystrophin and dystrophin-related protein 1 (DRP1 or utrophin). DRP2 is expressed principally in the brain and spinal cord. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":101219769,"end":101264497,"strand":1,"description":"dystrophin related protein 2 [Source:HGNC Symbol;Acc:HGNC:3032]"}, {"versioned_ensembl_gene_id":"ENSG00000185477.4","gene_symbol":"GPRIN3","gene_name":"GPRIN family member 3 [Source:HGNC Symbol;Acc:HGNC:27733]","synonyms":"GRIN3,FLJ42625","biotype":"protein_coding","ncbi_id":"285513","summary":null,"start":89236386,"end":89308010,"strand":-1,"description":"GPRIN family member 3 [Source:HGNC Symbol;Acc:HGNC:27733]"}, {"versioned_ensembl_gene_id":"ENSG00000243594.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"LMP2,RING12,beta1i,PSMB6i","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32772831,"end":32808281,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000135547.8","gene_symbol":"HEY2","gene_name":"hes related family bHLH transcription factor with YRPW motif 2 [Source:HGNC Symbol;Acc:HGNC:4881]","synonyms":"HESR2,HERP1,bHLHb32","biotype":"protein_coding","ncbi_id":"23493","summary":"This gene encodes a member of the hairy and enhancer of split-related (HESR) family of basic helix-loop-helix (bHLH)-type transcription factors. The encoded protein forms homo- or hetero-dimers that localize to the nucleus and interact with a histone deacetylase complex to repress transcription. Expression of this gene is induced by the Notch signal transduction pathway. Two similar and redundant genes in mouse are required for embryonic cardiovascular development, and are also implicated in neurogenesis and somitogenesis. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":125747664,"end":125761269,"strand":1,"description":"hes related family bHLH transcription factor with YRPW motif 2 [Source:HGNC Symbol;Acc:HGNC:4881]"}, {"versioned_ensembl_gene_id":"ENSG00000244146.1","gene_symbol":"AC106872.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164920618,"end":164921063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248652.2","gene_symbol":"AC034244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57081745,"end":57081951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105968.18","gene_symbol":"H2AFV","gene_name":"H2A histone family member V [Source:HGNC Symbol;Acc:HGNC:20664]","synonyms":"MGC1947,MGC10831,MGC10170,H2AV","biotype":"protein_coding","ncbi_id":"94239","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. Several transcript variants encoding different isoforms, have been identified for this gene. [provided by RefSeq, Oct 2015]","start":44826791,"end":44848083,"strand":-1,"description":"H2A histone family member V [Source:HGNC Symbol;Acc:HGNC:20664]"}, {"versioned_ensembl_gene_id":"ENSG00000258531.2","gene_symbol":"BANF1P1","gene_name":"barrier to autointegration factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20252]","synonyms":"D14S1460E,D14S1460,BCRP1,BCRG1","biotype":"processed_pseudogene","ncbi_id":"317687","summary":null,"start":68936602,"end":68936864,"strand":1,"description":"barrier to autointegration factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20252]"}, {"versioned_ensembl_gene_id":"ENSG00000281401.1","gene_symbol":"Z82185.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36816326,"end":36819736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182327.7","gene_symbol":"GLTPD2","gene_name":"glycolipid transfer protein domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33756]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388323","summary":null,"start":4788959,"end":4790390,"strand":1,"description":"glycolipid transfer protein domain containing 2 [Source:HGNC Symbol;Acc:HGNC:33756]"}, {"versioned_ensembl_gene_id":"ENSG00000260774.1","gene_symbol":"AC021087.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":213898,"end":217279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166801.15","gene_symbol":"FAM111A","gene_name":"family with sequence similarity 111 member A [Source:HGNC Symbol;Acc:HGNC:24725]","synonyms":"KIAA1895,FLJ22794","biotype":"protein_coding","ncbi_id":"63901","summary":"The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":59142748,"end":59155039,"strand":1,"description":"family with sequence similarity 111 member A [Source:HGNC Symbol;Acc:HGNC:24725]"}, {"versioned_ensembl_gene_id":"ENSG00000241571.2","gene_symbol":"ATP5A1P7","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37665]","synonyms":"ATP5A1P9","biotype":"processed_pseudogene","ncbi_id":"442415","summary":null,"start":62686912,"end":62688190,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37665]"}, {"versioned_ensembl_gene_id":"ENSG00000259630.2","gene_symbol":"AC104046.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":85415228,"end":85415633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197185.7","gene_symbol":"SSXP1","gene_name":"SSX family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30637]","synonyms":"psiSSX1","biotype":"unprocessed_pseudogene","ncbi_id":"100996564","summary":null,"start":52606535,"end":52611758,"strand":-1,"description":"SSX family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30637]"}, {"versioned_ensembl_gene_id":"ENSG00000235823.2","gene_symbol":"OLMALINC","gene_name":"oligodendrocyte maturation-associated long intergenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:28060]","synonyms":"NCRNA00263,LINC00263,HI-LNC80,FLJ12974,C10orf75,bA34D15.5","biotype":"lincRNA","ncbi_id":"90271","summary":null,"start":100373513,"end":100454043,"strand":1,"description":"oligodendrocyte maturation-associated long intergenic non-coding RNA [Source:HGNC Symbol;Acc:HGNC:28060]"}, {"versioned_ensembl_gene_id":"ENSG00000234305.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"hs6M1-4,OR6-5,dJ80I19.2,OR2J1P","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100980,"end":29101918,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000263603.1","gene_symbol":"AC127024.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30729469,"end":30731202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226463.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044245,"end":29045272,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000140526.17","gene_symbol":"ABHD2","gene_name":"abhydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18717]","synonyms":"LABH2","biotype":"protein_coding","ncbi_id":"11057","summary":"This gene encodes a protein containing an alpha/beta hydrolase fold, which is a catalytic domain found in a wide range of enzymes. The encoded protein is an acylglycerol lipase that catalyzes the hydrolysis of endocannabinoid arachidonoylglycerol from the cell membrane. This leads to activation of the sperm calcium channel CatSper, which results in sperm activation. Alternative splicing of this gene results in two transcript variants encoding the same protein. [provided by RefSeq, Jan 2017]","start":89087459,"end":89202360,"strand":1,"description":"abhydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18717]"}, {"versioned_ensembl_gene_id":"ENSG00000185608.8","gene_symbol":"MRPL40","gene_name":"mitochondrial ribosomal protein L40 [Source:HGNC Symbol;Acc:HGNC:14491]","synonyms":"NLVCF,MRP-L22","biotype":"protein_coding","ncbi_id":"64976","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Deletions in this gene may contribute to the etiology of velo-cardio-facial syndrome and DiGeorge syndrome. [provided by RefSeq, Jul 2008]","start":19431902,"end":19436075,"strand":1,"description":"mitochondrial ribosomal protein L40 [Source:HGNC Symbol;Acc:HGNC:14491]"}, {"versioned_ensembl_gene_id":"ENSG00000234451.1","gene_symbol":"BX005266.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62609725,"end":62610799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229500.1","gene_symbol":"RPL17P1","gene_name":"ribosomal protein L17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16559]","synonyms":"dJ1178H5.1","biotype":"processed_pseudogene","ncbi_id":"140748","summary":null,"start":20253303,"end":20253838,"strand":-1,"description":"ribosomal protein L17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16559]"}, {"versioned_ensembl_gene_id":"ENSG00000241054.1","gene_symbol":"AL035454.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20094401,"end":20095684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278160.1","gene_symbol":"BX510359.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52481515,"end":52483950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174606.13","gene_symbol":"ANGEL2","gene_name":"angel homolog 2 [Source:HGNC Symbol;Acc:HGNC:30534]","synonyms":"KIAA0759L,FLJ12793,Ccr4d","biotype":"protein_coding","ncbi_id":"90806","summary":null,"start":212992182,"end":213015826,"strand":-1,"description":"angel homolog 2 [Source:HGNC Symbol;Acc:HGNC:30534]"}, {"versioned_ensembl_gene_id":"ENSG00000006047.12","gene_symbol":"YBX2","gene_name":"Y-box binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17948]","synonyms":"Contrin,MSY2,CSDA3","biotype":"protein_coding","ncbi_id":"51087","summary":"This gene encodes a nucleic acid binding protein which is highly expressed in germ cells. The encoded protein binds to a Y-box element in the promoters of certain genes but also binds to mRNA transcribed from these genes. Pseudogenes for this gene are located on chromosome 10 and 15. [provided by RefSeq, Feb 2012]","start":7288252,"end":7294615,"strand":-1,"description":"Y-box binding protein 2 [Source:HGNC Symbol;Acc:HGNC:17948]"}, {"versioned_ensembl_gene_id":"ENSG00000241815.1","gene_symbol":"AC107015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96566357,"end":96567103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232419.1","gene_symbol":"TTTY19","gene_name":"testis-specific transcript, Y-linked 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18843]","synonyms":"NCRNA00144","biotype":"lincRNA","ncbi_id":"252952","summary":null,"start":8704472,"end":8705283,"strand":1,"description":"testis-specific transcript, Y-linked 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18843]"}, {"versioned_ensembl_gene_id":"ENSG00000258642.1","gene_symbol":"AL133371.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20874305,"end":20875768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185028.3","gene_symbol":"LRRC14B","gene_name":"leucine rich repeat containing 14B [Source:HGNC Symbol;Acc:HGNC:37268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389257","summary":"The protein encoded by this gene is a leucine-rich repeat containing protein that is a member of the PRAME family. [provided by RefSeq, Apr 2017]","start":191511,"end":195353,"strand":1,"description":"leucine rich repeat containing 14B [Source:HGNC Symbol;Acc:HGNC:37268]"}, {"versioned_ensembl_gene_id":"ENSG00000100084.14","gene_symbol":"HIRA","gene_name":"histone cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:4916]","synonyms":"TUPLE1,TUP1,DGCR1","biotype":"protein_coding","ncbi_id":"7290","summary":"This gene encodes a histone chaperone that preferentially places the variant histone H3.3 in nucleosomes. Orthologs of this gene in yeast, flies, and plants are necessary for the formation of transcriptionally silent heterochomatin. This gene plays an important role in the formation of the senescence-associated heterochromatin foci. These foci likely mediate the irreversible cell cycle changes that occur in senescent cells. It is considered the primary candidate gene in some haploinsufficiency syndromes such as DiGeorge syndrome, and insufficient production of the gene may disrupt normal embryonic development. [provided by RefSeq, Jul 2008]","start":19330698,"end":19447450,"strand":-1,"description":"histone cell cycle regulator [Source:HGNC Symbol;Acc:HGNC:4916]"}, {"versioned_ensembl_gene_id":"ENSG00000259130.1","gene_symbol":"AL133371.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20870278,"end":20873592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238061.2","gene_symbol":"AL356273.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":185280844,"end":185281816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164588.6","gene_symbol":"HCN1","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium channel 1 [Source:HGNC Symbol;Acc:HGNC:4845]","synonyms":"HAC-2,BCNG1,BCNG-1","biotype":"protein_coding","ncbi_id":"348980","summary":"The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011]","start":45254950,"end":45696498,"strand":-1,"description":"hyperpolarization activated cyclic nucleotide gated potassium channel 1 [Source:HGNC Symbol;Acc:HGNC:4845]"}, {"versioned_ensembl_gene_id":"ENSG00000113758.13","gene_symbol":"DBN1","gene_name":"drebrin 1 [Source:HGNC Symbol;Acc:HGNC:2695]","synonyms":"D0S117E","biotype":"protein_coding","ncbi_id":"1627","summary":"The protein encoded by this gene is a cytoplasmic actin-binding protein thought to play a role in the process of neuronal growth. It is a member of the drebrin family of proteins that are developmentally regulated in the brain. A decrease in the amount of this protein in the brain has been implicated as a possible contributing factor in the pathogenesis of memory disturbance in Alzheimer's disease. At least two alternative splice variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":177456608,"end":177474401,"strand":-1,"description":"drebrin 1 [Source:HGNC Symbol;Acc:HGNC:2695]"}, {"versioned_ensembl_gene_id":"ENSG00000198814.12","gene_symbol":"GK","gene_name":"glycerol kinase [Source:HGNC Symbol;Acc:HGNC:4289]","synonyms":"GKD,GK1","biotype":"protein_coding","ncbi_id":"2710","summary":"The protein encoded by this gene belongs to the FGGY kinase family. This protein is a key enzyme in the regulation of glycerol uptake and metabolism. It catalyzes the phosphorylation of glycerol by ATP, yielding ADP and glycerol-3-phosphate. Mutations in this gene are associated with glycerol kinase deficiency (GKD). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":30653359,"end":30731456,"strand":1,"description":"glycerol kinase [Source:HGNC Symbol;Acc:HGNC:4289]"}, {"versioned_ensembl_gene_id":"ENSG00000275250.1","gene_symbol":"AC093913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34714270,"end":34714598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255105.1","gene_symbol":"AC007751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103559099,"end":103559389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146276.11","gene_symbol":"GABRR1","gene_name":"gamma-aminobutyric acid type A receptor rho1 subunit [Source:HGNC Symbol;Acc:HGNC:4090]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2569","summary":"GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA receptors, which are ligand-gated chloride channels. GABRR1 is a member of the rho subunit family. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":89177501,"end":89231278,"strand":-1,"description":"gamma-aminobutyric acid type A receptor rho1 subunit [Source:HGNC Symbol;Acc:HGNC:4090]"}, {"versioned_ensembl_gene_id":"ENSG00000253477.5","gene_symbol":"AC012213.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103483398,"end":103501676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249654.1","gene_symbol":"VN1R104P","gene_name":"vomeronasal 1 receptor 104 pseudogene [Source:HGNC Symbol;Acc:HGNC:37427]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288195","summary":null,"start":54320204,"end":54321212,"strand":-1,"description":"vomeronasal 1 receptor 104 pseudogene [Source:HGNC Symbol;Acc:HGNC:37427]"}, {"versioned_ensembl_gene_id":"ENSG00000235875.3","gene_symbol":"ARHGEF7-AS2","gene_name":"ARHGEF7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40717]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874238","summary":null,"start":111113812,"end":111115678,"strand":-1,"description":"ARHGEF7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40717]"}, {"versioned_ensembl_gene_id":"ENSG00000239961.2","gene_symbol":"LILRA4","gene_name":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]","synonyms":"ILT7,CD85g","biotype":"protein_coding","ncbi_id":"23547","summary":"This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015]","start":54333185,"end":54339150,"strand":-1,"description":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]"}, {"versioned_ensembl_gene_id":"ENSG00000267098.1","gene_symbol":"AC113137.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60630167,"end":60902726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169020.9","gene_symbol":"ATP5I","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit E [Source:HGNC Symbol;Acc:HGNC:846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"521","summary":"Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the e subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]","start":672436,"end":674338,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit E [Source:HGNC Symbol;Acc:HGNC:846]"}, {"versioned_ensembl_gene_id":"ENSG00000129925.10","gene_symbol":"TMEM8A","gene_name":"transmembrane protein 8A [Source:HGNC Symbol;Acc:HGNC:17205]","synonyms":"TMEM8,TMEM6,M83","biotype":"protein_coding","ncbi_id":"58986","summary":null,"start":370773,"end":387113,"strand":-1,"description":"transmembrane protein 8A [Source:HGNC Symbol;Acc:HGNC:17205]"}, {"versioned_ensembl_gene_id":"ENSG00000267400.1","gene_symbol":"AC010928.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60495868,"end":60496336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251431.1","gene_symbol":"AC245884.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54298105,"end":54298814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253766.1","gene_symbol":"AC091946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21616262,"end":21779522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213430.6","gene_symbol":"HSPD1P1","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35133]","synonyms":"HSPD1-2P","biotype":"processed_pseudogene","ncbi_id":"643300","summary":null,"start":21882585,"end":21884310,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35133]"}, {"versioned_ensembl_gene_id":"ENSG00000109107.13","gene_symbol":"ALDOC","gene_name":"aldolase, fructose-bisphosphate C [Source:HGNC Symbol;Acc:HGNC:418]","synonyms":null,"biotype":"protein_coding","ncbi_id":"230","summary":"This gene encodes a member of the class I fructose-biphosphate aldolase gene family. Expressed specifically in the hippocampus and Purkinje cells of the brain, the encoded protein is a glycolytic enzyme that catalyzes the reversible aldol cleavage of fructose-1,6-biphosphate and fructose 1-phosphate to dihydroxyacetone phosphate and either glyceraldehyde-3-phosphate or glyceraldehyde, respectively. [provided by RefSeq, Jul 2008]","start":28573115,"end":28577264,"strand":-1,"description":"aldolase, fructose-bisphosphate C [Source:HGNC Symbol;Acc:HGNC:418]"}, {"versioned_ensembl_gene_id":"ENSG00000250122.1","gene_symbol":"AC122694.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45890216,"end":45895970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227094.1","gene_symbol":"AL512785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162316852,"end":162317794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111181.12","gene_symbol":"SLC6A12","gene_name":"solute carrier family 6 member 12 [Source:HGNC Symbol;Acc:HGNC:11045]","synonyms":"BGT-1","biotype":"protein_coding","ncbi_id":"6539","summary":null,"start":190077,"end":214570,"strand":-1,"description":"solute carrier family 6 member 12 [Source:HGNC Symbol;Acc:HGNC:11045]"}, {"versioned_ensembl_gene_id":"ENSG00000239887.4","gene_symbol":"C1orf226","gene_name":"chromosome 1 open reading frame 226 [Source:HGNC Symbol;Acc:HGNC:34351]","synonyms":"FLJ13137","biotype":"protein_coding","ncbi_id":"400793","summary":null,"start":162366908,"end":162386818,"strand":1,"description":"chromosome 1 open reading frame 226 [Source:HGNC Symbol;Acc:HGNC:34351]"}, {"versioned_ensembl_gene_id":"ENSG00000238288.1","gene_symbol":"MTND3P23","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52169]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075295","summary":null,"start":92110168,"end":92110514,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52169]"}, {"versioned_ensembl_gene_id":"ENSG00000253366.3","gene_symbol":"AC139272.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70751184,"end":70795914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214717.11","gene_symbol":"ZBED1","gene_name":"zinc finger BED-type containing 1 [Source:HGNC Symbol;Acc:HGNC:447]","synonyms":"KIAA0785,hDREF,DREF,ALTE,TRAMP","biotype":"protein_coding","ncbi_id":"9189","summary":"This gene is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. It was earlier identified as a gene with similarity to Ac transposable elements, however, was found not to have transposase activity. Later studies show that this gene product is localized in the nucleus and functions as a transcription factor. It binds to DNA elements found in the promoter regions of several genes related to cell proliferation, such as histone H1, hence may have a role in regulating genes related to cell proliferation. Alternatively spliced transcript variants with different 5' untranslated region have been found for this gene. [provided by RefSeq, Jan 2010]","start":2486414,"end":2500967,"strand":-1,"description":"zinc finger BED-type containing 1 [Source:HGNC Symbol;Acc:HGNC:447]"}, {"versioned_ensembl_gene_id":"ENSG00000011275.18","gene_symbol":"RNF216","gene_name":"ring finger protein 216 [Source:HGNC Symbol;Acc:HGNC:21698]","synonyms":"ZIN,UBCE7IP1,TRIAD3","biotype":"protein_coding","ncbi_id":"54476","summary":"This gene encodes a cytoplasmic protein which specifically colocalizes and interacts with the serine/threonine protein kinase, receptor-interacting protein (RIP). Zinc finger domains of the encoded protein are required for its interaction with RIP and for inhibition of TNF- and IL1-induced NF-kappa B activation pathways. The encoded protein may also function as an E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes and transfers it to substrates. Several alternatively spliced transcript variants have been described for this locus but the full-length natures of only some are known. [provided by RefSeq, Jul 2008]","start":5620047,"end":5781739,"strand":-1,"description":"ring finger protein 216 [Source:HGNC Symbol;Acc:HGNC:21698]"}, {"versioned_ensembl_gene_id":"ENSG00000170624.13","gene_symbol":"SGCD","gene_name":"sarcoglycan delta [Source:HGNC Symbol;Acc:HGNC:10807]","synonyms":"DAGD,CMD1L,LGMD2F","biotype":"protein_coding","ncbi_id":"6444","summary":"The protein encoded by this gene is one of the four known components of the sarcoglycan complex, which is a subcomplex of the dystrophin-glycoprotein complex (DGC). DGC forms a link between the F-actin cytoskeleton and the extracellular matrix. This protein is expressed most abundantly in skeletal and cardiac muscle. Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene. [provided by RefSeq, Jul 2008]","start":155870344,"end":156767788,"strand":1,"description":"sarcoglycan delta [Source:HGNC Symbol;Acc:HGNC:10807]"}, {"versioned_ensembl_gene_id":"ENSG00000254163.1","gene_symbol":"AC025434.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156704058,"end":156739812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239689.1","gene_symbol":"AC015864.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50823577,"end":50824120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227674.1","gene_symbol":"LINC00355","gene_name":"long intergenic non-protein coding RNA 355 [Source:HGNC Symbol;Acc:HGNC:27061]","synonyms":null,"biotype":"lincRNA","ncbi_id":"144766","summary":null,"start":63986371,"end":64076011,"strand":-1,"description":"long intergenic non-protein coding RNA 355 [Source:HGNC Symbol;Acc:HGNC:27061]"}, {"versioned_ensembl_gene_id":"ENSG00000174672.15","gene_symbol":"BRSK2","gene_name":"BR serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:11405]","synonyms":"STK29,PEN11B,C11orf7","biotype":"protein_coding","ncbi_id":"9024","summary":null,"start":1389899,"end":1462689,"strand":1,"description":"BR serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:11405]"}, {"versioned_ensembl_gene_id":"ENSG00000124568.10","gene_symbol":"SLC17A1","gene_name":"solute carrier family 17 member 1 [Source:HGNC Symbol;Acc:HGNC:10929]","synonyms":"NPT1,NAPI-1","biotype":"protein_coding","ncbi_id":"6568","summary":null,"start":25782897,"end":25832059,"strand":-1,"description":"solute carrier family 17 member 1 [Source:HGNC Symbol;Acc:HGNC:10929]"}, {"versioned_ensembl_gene_id":"ENSG00000178093.13","gene_symbol":"TSSK6","gene_name":"testis specific serine kinase 6 [Source:HGNC Symbol;Acc:HGNC:30410]","synonyms":"SSTK,FLJ24002,CT72","biotype":"protein_coding","ncbi_id":"83983","summary":"This intronless gene encodes a member of the CAMK (calcium/calmodulin-dependent) serine/threonine protein kinase family. The encoded kinase has a broad expression pattern but is described as testis-specific due to effects on fertility. Male mice which lack the gene encoding a highly similar protein are sterile and have morphologically abnormal sperm. [provided by RefSeq, Jan 2012]","start":19512418,"end":19515685,"strand":-1,"description":"testis specific serine kinase 6 [Source:HGNC Symbol;Acc:HGNC:30410]"}, {"versioned_ensembl_gene_id":"ENSG00000280088.1","gene_symbol":"AC126474.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":100032325,"end":100034074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249937.5","gene_symbol":"LINC02223","gene_name":"long intergenic non-protein coding RNA 2223 [Source:HGNC Symbol;Acc:HGNC:53092]","synonyms":null,"biotype":"lincRNA","ncbi_id":"646241","summary":null,"start":17684584,"end":17955857,"strand":1,"description":"long intergenic non-protein coding RNA 2223 [Source:HGNC Symbol;Acc:HGNC:53092]"}, {"versioned_ensembl_gene_id":"ENSG00000172769.3","gene_symbol":"OR5B3","gene_name":"olfactory receptor family 5 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8324]","synonyms":"OST129,OR5B13","biotype":"protein_coding","ncbi_id":"441608","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58402464,"end":58406874,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8324]"}, {"versioned_ensembl_gene_id":"ENSG00000235635.1","gene_symbol":"AC016644.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56941307,"end":56947152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228648.1","gene_symbol":"AL353747.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167241891,"end":167245916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149403.12","gene_symbol":"GRIK4","gene_name":"glutamate ionotropic receptor kainate type subunit 4 [Source:HGNC Symbol;Acc:HGNC:4582]","synonyms":"KA1,GRIK,GluK4","biotype":"protein_coding","ncbi_id":"2900","summary":"This gene encodes a protein that belongs to the glutamate-gated ionic channel family. Glutamate functions as the major excitatory neurotransmitter in the central nervous system through activation of ligand-gated ion channels and G protein-coupled membrane receptors. The protein encoded by this gene forms functional heteromeric kainate-preferring ionic channels with the subunits encoded by related gene family members. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":120511700,"end":120988904,"strand":1,"description":"glutamate ionotropic receptor kainate type subunit 4 [Source:HGNC Symbol;Acc:HGNC:4582]"}, {"versioned_ensembl_gene_id":"ENSG00000050628.20","gene_symbol":"PTGER3","gene_name":"prostaglandin E receptor 3 [Source:HGNC Symbol;Acc:HGNC:9595]","synonyms":"EP3","biotype":"protein_coding","ncbi_id":"5733","summary":"The protein encoded by this gene is a member of the G-protein coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). This receptor may have many biological functions, which involve digestion, nervous system, kidney reabsorption, and uterine contraction activities. Studies of the mouse counterpart suggest that this receptor may also mediate adrenocorticotropic hormone response as well as fever generation in response to exogenous and endogenous stimuli. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":70852353,"end":71047808,"strand":-1,"description":"prostaglandin E receptor 3 [Source:HGNC Symbol;Acc:HGNC:9595]"}, {"versioned_ensembl_gene_id":"ENSG00000255337.1","gene_symbol":"AP001830.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102452919,"end":102462008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113649.11","gene_symbol":"TCERG1","gene_name":"transcription elongation regulator 1 [Source:HGNC Symbol;Acc:HGNC:15630]","synonyms":"Urn1,TAF2S,CA150","biotype":"protein_coding","ncbi_id":"10915","summary":"This gene encodes a nuclear protein that regulates transcriptional elongation and pre-mRNA splicing. The encoded protein interacts with the hyperphosphorylated C-terminal domain of RNA polymerase II via multiple FF domains, and with the pre-mRNA splicing factor SF1 via a WW domain. Alternative splicing results in multiple transcripts variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":146447311,"end":146511961,"strand":1,"description":"transcription elongation regulator 1 [Source:HGNC Symbol;Acc:HGNC:15630]"}, {"versioned_ensembl_gene_id":"ENSG00000255006.1","gene_symbol":"ELOCP22","gene_name":"elongin C pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:38158]","synonyms":"TCEB1P22","biotype":"processed_pseudogene","ncbi_id":"100287579","summary":null,"start":120619934,"end":120620267,"strand":-1,"description":"elongin C pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:38158]"}, {"versioned_ensembl_gene_id":"ENSG00000223806.7","gene_symbol":"LINC00114","gene_name":"long intergenic non-protein coding RNA 114 [Source:HGNC Symbol;Acc:HGNC:1265]","synonyms":"NCRNA00114,C21orf24","biotype":"lincRNA","ncbi_id":"400866","summary":null,"start":38739021,"end":38747460,"strand":-1,"description":"long intergenic non-protein coding RNA 114 [Source:HGNC Symbol;Acc:HGNC:1265]"}, {"versioned_ensembl_gene_id":"ENSG00000279148.1","gene_symbol":"AC126474.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":100026248,"end":100027540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259466.1","gene_symbol":"NPM1P47","gene_name":"nucleophosmin 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45226]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129972","summary":null,"start":62082450,"end":62083305,"strand":-1,"description":"nucleophosmin 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:45226]"}, {"versioned_ensembl_gene_id":"ENSG00000135655.15","gene_symbol":"USP15","gene_name":"ubiquitin specific peptidase 15 [Source:HGNC Symbol;Acc:HGNC:12613]","synonyms":"UNPH4,KIAA0529","biotype":"protein_coding","ncbi_id":"9958","summary":"This gene encodes a member of the ubiquitin specific protease (USP) family of deubiquitinating enzymes. USP enzymes play critical roles in ubiquitin-dependent processes through polyubiquitin chain disassembly and hydrolysis of ubiquitin-substrate bonds. The encoded protein associates with the COP9 signalosome, and also plays a role in transforming growth factor beta signalling through deubiquitination of receptor-activated SMAD transcription factors. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 2. [provided by RefSeq, Nov 2011]","start":62260338,"end":62417431,"strand":1,"description":"ubiquitin specific peptidase 15 [Source:HGNC Symbol;Acc:HGNC:12613]"}, {"versioned_ensembl_gene_id":"ENSG00000196118.11","gene_symbol":"CCDC189","gene_name":"coiled-coil domain containing 189 [Source:HGNC Symbol;Acc:HGNC:28078]","synonyms":"MGC104706,C16orf93","biotype":"protein_coding","ncbi_id":"90835","summary":null,"start":30757423,"end":30762710,"strand":-1,"description":"coiled-coil domain containing 189 [Source:HGNC Symbol;Acc:HGNC:28078]"}, {"versioned_ensembl_gene_id":"ENSG00000182489.8","gene_symbol":"XKRX","gene_name":"XK related, X-linked [Source:HGNC Symbol;Acc:HGNC:29845]","synonyms":"XPLAC,XKR2","biotype":"protein_coding","ncbi_id":"402415","summary":"This gene encodes a protein that is related to a component of the XK/Kell complex of the Kell blood group system. The encoded protein includes several transmembrane domains, is known to be exposed to the cell surface, and may function as a membrane transporter. [provided by RefSeq, May 2010]","start":100913445,"end":100929433,"strand":-1,"description":"XK related, X-linked [Source:HGNC Symbol;Acc:HGNC:29845]"}, {"versioned_ensembl_gene_id":"ENSG00000164047.4","gene_symbol":"CAMP","gene_name":"cathelicidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:1472]","synonyms":"LL37,FALL39,FALL-39,CAP18","biotype":"protein_coding","ncbi_id":"820","summary":"This gene encodes a member of an antimicrobial peptide family, characterized by a highly conserved N-terminal signal peptide containing a cathelin domain and a structurally variable cationic antimicrobial peptide, which is produced by extracellular proteolysis from the C-terminus. In addition to its antibacterial, antifungal, and antiviral activities, the encoded protein functions in cell chemotaxis, immune mediator induction, and inflammatory response regulation. [provided by RefSeq, Sep 2014]","start":48223347,"end":48225491,"strand":1,"description":"cathelicidin antimicrobial peptide [Source:HGNC Symbol;Acc:HGNC:1472]"}, {"versioned_ensembl_gene_id":"ENSG00000235143.1","gene_symbol":"AL445235.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30858158,"end":30860254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129007.14","gene_symbol":"CALML4","gene_name":"calmodulin like 4 [Source:HGNC Symbol;Acc:HGNC:18445]","synonyms":"NY-BR-20,MGC4809","biotype":"protein_coding","ncbi_id":"91860","summary":null,"start":68190705,"end":68206110,"strand":-1,"description":"calmodulin like 4 [Source:HGNC Symbol;Acc:HGNC:18445]"}, {"versioned_ensembl_gene_id":"ENSG00000071189.21","gene_symbol":"SNX13","gene_name":"sorting nexin 13 [Source:HGNC Symbol;Acc:HGNC:21335]","synonyms":"KIAA0713,RGS-PX1","biotype":"protein_coding","ncbi_id":"23161","summary":"This gene encodes a PHOX domain- and RGS domain-containing protein that belongs to the sorting nexin (SNX) family and the regulator of G protein signaling (RGS) family. The PHOX domain is a phosphoinositide binding domain, and the SNX family members are involved in intracellular trafficking. The RGS family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. The RGS domain of this protein interacts with G alpha(s), accelerates its GTP hydrolysis, and attenuates G alpha(s)-mediated signaling. Overexpression of this protein delayes lysosomal degradation of the epidermal growth factor receptor. Because of its bifunctional role, this protein may link heterotrimeric G protein signaling and vesicular trafficking. [provided by RefSeq, Jul 2008]","start":17790761,"end":17940501,"strand":-1,"description":"sorting nexin 13 [Source:HGNC Symbol;Acc:HGNC:21335]"}, {"versioned_ensembl_gene_id":"ENSG00000282720.1","gene_symbol":"AC243301.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":386179,"end":389829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236272.1","gene_symbol":"Z82214.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43212674,"end":43213661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242941.1","gene_symbol":"RPL12P7","gene_name":"ribosomal protein L12 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326275","summary":null,"start":68693090,"end":68693583,"strand":1,"description":"ribosomal protein L12 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:19782]"}, {"versioned_ensembl_gene_id":"ENSG00000255218.1","gene_symbol":"OR5BC1P","gene_name":"olfactory receptor family 5 subfamily BC member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15272]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81208","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58317637,"end":58318375,"strand":-1,"description":"olfactory receptor family 5 subfamily BC member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15272]"}, {"versioned_ensembl_gene_id":"ENSG00000204519.10","gene_symbol":"ZNF551","gene_name":"zinc finger protein 551 [Source:HGNC Symbol;Acc:HGNC:25108]","synonyms":"DKFZp686H1038","biotype":"protein_coding","ncbi_id":"90233","summary":null,"start":57681969,"end":57717301,"strand":1,"description":"zinc finger protein 551 [Source:HGNC Symbol;Acc:HGNC:25108]"}, {"versioned_ensembl_gene_id":"ENSG00000140511.11","gene_symbol":"HAPLN3","gene_name":"hyaluronan and proteoglycan link protein 3 [Source:HGNC Symbol;Acc:HGNC:21446]","synonyms":"HsT19883,EXLD1","biotype":"protein_coding","ncbi_id":"145864","summary":"This gene belongs to the hyaluronan and proteoglycan binding link protein gene family. The protein encoded by this gene may function in hyaluronic acid binding and cell adhesion. [provided by RefSeq, Jul 2008]","start":88877288,"end":88895626,"strand":-1,"description":"hyaluronan and proteoglycan link protein 3 [Source:HGNC Symbol;Acc:HGNC:21446]"}, {"versioned_ensembl_gene_id":"ENSG00000185761.10","gene_symbol":"ADAMTSL5","gene_name":"ADAMTS like 5 [Source:HGNC Symbol;Acc:HGNC:27912]","synonyms":"THSD6","biotype":"protein_coding","ncbi_id":"339366","summary":null,"start":1505018,"end":1513604,"strand":-1,"description":"ADAMTS like 5 [Source:HGNC Symbol;Acc:HGNC:27912]"}, {"versioned_ensembl_gene_id":"ENSG00000267092.2","gene_symbol":"AC027307.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1508375,"end":1508963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152936.10","gene_symbol":"LMNTD1","gene_name":"lamin tail domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26683]","synonyms":"Pas1c1,IFLTD1,FLJ36004","biotype":"protein_coding","ncbi_id":"160492","summary":null,"start":25409307,"end":25648579,"strand":-1,"description":"lamin tail domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26683]"}, {"versioned_ensembl_gene_id":"ENSG00000257308.1","gene_symbol":"AC090017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61231159,"end":61232937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147419.17","gene_symbol":"CCDC25","gene_name":"coiled-coil domain containing 25 [Source:HGNC Symbol;Acc:HGNC:25591]","synonyms":"FLJ10853","biotype":"protein_coding","ncbi_id":"55246","summary":null,"start":27733311,"end":27772653,"strand":-1,"description":"coiled-coil domain containing 25 [Source:HGNC Symbol;Acc:HGNC:25591]"}, {"versioned_ensembl_gene_id":"ENSG00000171903.16","gene_symbol":"CYP4F11","gene_name":"cytochrome P450 family 4 subfamily F member 11 [Source:HGNC Symbol;Acc:HGNC:13265]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57834","summary":"This gene, CYP4F11, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F2, is approximately 16 kb away. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":15912367,"end":15934867,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 11 [Source:HGNC Symbol;Acc:HGNC:13265]"}, {"versioned_ensembl_gene_id":"ENSG00000259790.1","gene_symbol":"ANP32BP1","gene_name":"acidic nuclear phosphoprotein 32 family member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24267]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"646791","summary":null,"start":75321397,"end":75322693,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24267]"}, {"versioned_ensembl_gene_id":"ENSG00000180532.10","gene_symbol":"ZSCAN4","gene_name":"zinc finger and SCAN domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23709]","synonyms":"ZNF494,FLJ35105","biotype":"protein_coding","ncbi_id":"201516","summary":"The ZSCAN4 gene encodes a protein involved in telomere maintenance and with a key role in the critical feature of mouse embryonic stem (ES) cells, namely, defying cellular senescence and maintaining normal karyotype for many cell divisions in culture (Zalzman et al., 2010 [PubMed 20336070]).[supplied by OMIM, May 2010]","start":57668935,"end":57679152,"strand":1,"description":"zinc finger and SCAN domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23709]"}, {"versioned_ensembl_gene_id":"ENSG00000080603.16","gene_symbol":"SRCAP","gene_name":"Snf2 related CREBBP activator protein [Source:HGNC Symbol;Acc:HGNC:16974]","synonyms":"SWR1,KIAA0309,EAF1,DOMO1","biotype":"protein_coding","ncbi_id":"10847","summary":"This gene encodes the core catalytic component of the multiprotein chromatin-remodeling SRCAP complex. The encoded protein is an ATPase that is necessary for the incorporation of the histone variant H2A.Z into nucleosomes. It can function as a transcriptional activator in Notch-mediated, CREB-mediated and steroid receptor-mediated transcription. Mutations in this gene cause Floating-Harbor syndrome, a rare disorder characterized by short stature, language deficits and dysmorphic facial features. [provided by RefSeq, Feb 2012]","start":30698209,"end":30741409,"strand":1,"description":"Snf2 related CREBBP activator protein [Source:HGNC Symbol;Acc:HGNC:16974]"}, {"versioned_ensembl_gene_id":"ENSG00000178723.7","gene_symbol":"GLULP4","gene_name":"glutamate-ammonia ligase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4345]","synonyms":"GLULP","biotype":"processed_pseudogene","ncbi_id":"392305","summary":null,"start":34917175,"end":34918296,"strand":1,"description":"glutamate-ammonia ligase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4345]"}, {"versioned_ensembl_gene_id":"ENSG00000259237.1","gene_symbol":"LINC02490","gene_name":"long intergenic non-protein coding RNA 2490 [Source:HGNC Symbol;Acc:HGNC:53471]","synonyms":"RP11-209E8","biotype":"lincRNA","ncbi_id":"105370822","summary":null,"start":53116365,"end":53129698,"strand":1,"description":"long intergenic non-protein coding RNA 2490 [Source:HGNC Symbol;Acc:HGNC:53471]"}, {"versioned_ensembl_gene_id":"ENSG00000253880.1","gene_symbol":"AC009435.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6044353,"end":6257537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271533.1","gene_symbol":"Z83843.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":74209976,"end":74213660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282611.1","gene_symbol":"CNN2P12","gene_name":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131550","summary":null,"start":18726706,"end":18727414,"strand":1,"description":"calponin 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39834]"}, {"versioned_ensembl_gene_id":"ENSG00000233984.1","gene_symbol":"RPSAP14","gene_name":"ribosomal protein SA pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6506]","synonyms":"LAMRP4,LAMRL4,LAMR1P14","biotype":"processed_pseudogene","ncbi_id":"3924","summary":null,"start":74031462,"end":74031820,"strand":1,"description":"ribosomal protein SA pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:6506]"}, {"versioned_ensembl_gene_id":"ENSG00000282043.1","gene_symbol":"AC003103.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37036498,"end":37045083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282037.1","gene_symbol":"GXYLT1P1","gene_name":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101111","summary":null,"start":18724415,"end":18724904,"strand":-1,"description":"glucoside xylosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39676]"}, {"versioned_ensembl_gene_id":"ENSG00000198498.9","gene_symbol":"TMA16","gene_name":"translation machinery associated 16 homolog [Source:HGNC Symbol;Acc:HGNC:25638]","synonyms":"FLJ11184,C4orf43","biotype":"protein_coding","ncbi_id":"55319","summary":null,"start":163494442,"end":163520539,"strand":1,"description":"translation machinery associated 16 homolog [Source:HGNC Symbol;Acc:HGNC:25638]"}, {"versioned_ensembl_gene_id":"ENSG00000274821.4","gene_symbol":"SERPINA2","gene_name":"serpin family A member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8985]","synonyms":"SERPINA2P,PIL,ATR,ARGS","biotype":"protein_coding","ncbi_id":"390502","summary":"This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. The encoded intracellular glycoprotein is localized at the endoplasmic reticulum. This gene is a polymorphic pseudogene, with the non-functional allele being predominant in some populations. Some individuals, as represented by the reference genome allele, contain a 2kb coding region deletion and a start code mutation. [provided by RefSeq, Feb 2014]","start":94363640,"end":94374417,"strand":-1,"description":"serpin family A member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8985]"}, {"versioned_ensembl_gene_id":"ENSG00000256661.1","gene_symbol":"A2ML1-AS1","gene_name":"A2ML1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41022]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874108","summary":null,"start":8776219,"end":8830947,"strand":-1,"description":"A2ML1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41022]"}, {"versioned_ensembl_gene_id":"ENSG00000224515.1","gene_symbol":"AL590385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161556290,"end":161557078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254553.1","gene_symbol":"AL033529.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32465057,"end":32600792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244131.2","gene_symbol":"RPSAP51","gene_name":"ribosomal protein SA pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36224]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271267","summary":null,"start":8742428,"end":8743072,"strand":1,"description":"ribosomal protein SA pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:36224]"}, {"versioned_ensembl_gene_id":"ENSG00000203620.2","gene_symbol":"AL354919.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31842019,"end":31855568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282022.1","gene_symbol":"AC006581.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8858143,"end":8915276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260278.1","gene_symbol":"AC098818.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78773654,"end":78775973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121406.8","gene_symbol":"ZNF549","gene_name":"zinc finger protein 549 [Source:HGNC Symbol;Acc:HGNC:26632]","synonyms":"FLJ34917","biotype":"protein_coding","ncbi_id":"256051","summary":null,"start":57527325,"end":57557542,"strand":1,"description":"zinc finger protein 549 [Source:HGNC Symbol;Acc:HGNC:26632]"}, {"versioned_ensembl_gene_id":"ENSG00000268628.2","gene_symbol":"AL121761.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19756390,"end":19758037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233895.1","gene_symbol":"AL121761.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19757708,"end":19809675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118160.13","gene_symbol":"SLC8A2","gene_name":"solute carrier family 8 member A2 [Source:HGNC Symbol;Acc:HGNC:11069]","synonyms":"NCX2,KIAA1087","biotype":"protein_coding","ncbi_id":"6543","summary":null,"start":47428017,"end":47472168,"strand":-1,"description":"solute carrier family 8 member A2 [Source:HGNC Symbol;Acc:HGNC:11069]"}, {"versioned_ensembl_gene_id":"ENSG00000236466.1","gene_symbol":"AL359633.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46492052,"end":46532758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265417.1","gene_symbol":"AP005119.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1362445,"end":1363873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184007.18","gene_symbol":"PTP4A2","gene_name":"protein tyrosine phosphatase type IVA, member 2 [Source:HGNC Symbol;Acc:HGNC:9635]","synonyms":"PTPCAAX2,PTP4A,ptp-IV1a,PRL-2,OV-1,HU-PP-1","biotype":"protein_coding","ncbi_id":"8073","summary":"The protein encoded by this gene belongs to a small class of the protein tyrosine phosphatase (PTP) family. PTPs are cell signaling molecules that play regulatory roles in a variety of cellular processes. PTPs in this class contain a protein tyrosine phosphatase catalytic domain and a characteristic C-terminal prenylation motif. This PTP has been shown to primarily associate with plasmic and endosomal membrane through its C-terminal prenylation. This PTP was found to interact with the beta-subunit of Rab geranylgeranyltransferase II (beta GGT II), and thus may function as a regulator of GGT II activity. Overexpression of this gene in mammalian cells conferred a transformed phenotype, which suggested its role in tumorigenesis. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 11, 12 and 17. [provided by RefSeq, Aug 2010]","start":31906421,"end":31944856,"strand":-1,"description":"protein tyrosine phosphatase type IVA, member 2 [Source:HGNC Symbol;Acc:HGNC:9635]"}, {"versioned_ensembl_gene_id":"ENSG00000162511.7","gene_symbol":"LAPTM5","gene_name":"lysosomal protein transmembrane 5 [Source:HGNC Symbol;Acc:HGNC:29612]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7805","summary":"This gene encodes a transmembrane receptor that is associated with lysosomes. The encoded protein, also known as E3 protein, may play a role in hematopoiesis. [provided by RefSeq, Feb 2009]","start":30732469,"end":30757820,"strand":-1,"description":"lysosomal protein transmembrane 5 [Source:HGNC Symbol;Acc:HGNC:29612]"}, {"versioned_ensembl_gene_id":"ENSG00000215771.2","gene_symbol":"LRRC37A14P","gene_name":"leucine rich repeat containing 37 member A14, pseudogene [Source:HGNC Symbol;Acc:HGNC:43818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479025","summary":null,"start":41189727,"end":41190188,"strand":-1,"description":"leucine rich repeat containing 37 member A14, pseudogene [Source:HGNC Symbol;Acc:HGNC:43818]"}, {"versioned_ensembl_gene_id":"ENSG00000164877.18","gene_symbol":"MICALL2","gene_name":"MICAL like 2 [Source:HGNC Symbol;Acc:HGNC:29672]","synonyms":"JRAB,FLJ23471,MICAL-L2,MGC46023","biotype":"protein_coding","ncbi_id":"79778","summary":null,"start":1428465,"end":1459502,"strand":-1,"description":"MICAL like 2 [Source:HGNC Symbol;Acc:HGNC:29672]"}, {"versioned_ensembl_gene_id":"ENSG00000197162.9","gene_symbol":"ZNF785","gene_name":"zinc finger protein 785 [Source:HGNC Symbol;Acc:HGNC:26496]","synonyms":"FLJ32130","biotype":"protein_coding","ncbi_id":"146540","summary":null,"start":30573740,"end":30585771,"strand":-1,"description":"zinc finger protein 785 [Source:HGNC Symbol;Acc:HGNC:26496]"}, {"versioned_ensembl_gene_id":"ENSG00000186187.11","gene_symbol":"ZNRF1","gene_name":"zinc and ring finger 1 [Source:HGNC Symbol;Acc:HGNC:18452]","synonyms":"nin283,FLJ14846,DKFZp434E229","biotype":"protein_coding","ncbi_id":"84937","summary":"This gene encodes an E3 ubiquitin-protein ligase that plays a role in neural-cell differentiation. Overexpression of this gene causes neurite-like elongation. The encoded protein contains both a zinc finger and a RING finger motif and is localized in the endosome/lysosome compartment, indicating that it may be involved in ubiquitin-mediated protein modification, and in synaptic vessicle membranes in neurons. [provided by RefSeq, Feb 2012]","start":74999030,"end":75110994,"strand":1,"description":"zinc and ring finger 1 [Source:HGNC Symbol;Acc:HGNC:18452]"}, {"versioned_ensembl_gene_id":"ENSG00000279544.1","gene_symbol":"AL133243.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32563328,"end":32566436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275197.1","gene_symbol":"AC092794.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25225103,"end":25225665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233243.1","gene_symbol":"AC112492.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27863893,"end":27864349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233724.1","gene_symbol":"AL513321.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65248032,"end":65248792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000050555.17","gene_symbol":"LAMC3","gene_name":"laminin subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:6494]","synonyms":"DKFZp434E202","biotype":"protein_coding","ncbi_id":"10319","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the gamma chain isoform laminin, gamma 3. The gamma 3 chain is most similar to the gamma 1 chain, and contains all the 6 domains expected of the gamma chain. It is a component of laminin 12. The gamma 3 chain is broadly expressed in skin, heart, lung, and the reproductive tracts. In skin, it is seen within the basement membrane of the dermal-epidermal junction at points of nerve penetration. Gamma 3 is also a prominent element of the apical surface of ciliated epithelial cells of lung, oviduct, epididymis, ductus deferens, and seminiferous tubules. The distribution of gamma 3-containing laminins along ciliated epithelial surfaces suggests that the apical laminins are important in the morphogenesis and structural stability of the ciliated processes of these cells. [provided by RefSeq, Aug 2011]","start":131009082,"end":131094473,"strand":1,"description":"laminin subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:6494]"}, {"versioned_ensembl_gene_id":"ENSG00000284439.1","gene_symbol":"AC106774.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17518367,"end":17518963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259330.2","gene_symbol":"INAFM2","gene_name":"InaF motif containing 2 [Source:HGNC Symbol;Acc:HGNC:35165]","synonyms":"OGU1,LINC00984","biotype":"protein_coding","ncbi_id":"100505573","summary":null,"start":40323664,"end":40326715,"strand":1,"description":"InaF motif containing 2 [Source:HGNC Symbol;Acc:HGNC:35165]"}, {"versioned_ensembl_gene_id":"ENSG00000211693.2","gene_symbol":"TRGV11","gene_name":"T-cell receptor gamma variable 11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12286]","synonyms":"V4P,TCRGV11","biotype":"TR_V_gene","ncbi_id":"6985","summary":null,"start":38291616,"end":38292078,"strand":-1,"description":"T-cell receptor gamma variable 11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12286]"}, {"versioned_ensembl_gene_id":"ENSG00000223637.7","gene_symbol":"RBMY2EP","gene_name":"RNA binding motif protein, Y-linked, family 2, member E pseudogene [Source:HGNC Symbol;Acc:HGNC:23890]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"159125","summary":null,"start":21394991,"end":21401585,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member E pseudogene [Source:HGNC Symbol;Acc:HGNC:23890]"}, {"versioned_ensembl_gene_id":"ENSG00000230873.8","gene_symbol":"STMND1","gene_name":"stathmin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44668]","synonyms":"FLJ23152","biotype":"protein_coding","ncbi_id":"401236","summary":null,"start":17102258,"end":17131372,"strand":1,"description":"stathmin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:44668]"}, {"versioned_ensembl_gene_id":"ENSG00000108819.10","gene_symbol":"PPP1R9B","gene_name":"protein phosphatase 1 regulatory subunit 9B [Source:HGNC Symbol;Acc:HGNC:9298]","synonyms":"Spn,SPINO,PPP1R9,PPP1R6","biotype":"protein_coding","ncbi_id":"84687","summary":"This gene encodes a scaffold protein that functions as a regulatory subunit of protein phosphatase 1a. Expression of this gene is particularly high in dendritic spines, suggesting that the encoded protein may play a role in receiving signals from the central nervous system. The encoded protein has putative tumor suppressor function and decreased expression has been observed in tumors. [provided by RefSeq, Feb 2014]","start":50133735,"end":50150630,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 9B [Source:HGNC Symbol;Acc:HGNC:9298]"}, {"versioned_ensembl_gene_id":"ENSG00000233306.2","gene_symbol":"TRGV2","gene_name":"T-cell receptor gamma variable 2 [Source:HGNC Symbol;Acc:HGNC:12287]","synonyms":"VIS2,TCRGV2","biotype":"TR_V_gene","ncbi_id":"6974","summary":null,"start":38362864,"end":38363518,"strand":-1,"description":"T-cell receptor gamma variable 2 [Source:HGNC Symbol;Acc:HGNC:12287]"}, {"versioned_ensembl_gene_id":"ENSG00000137747.15","gene_symbol":"TMPRSS13","gene_name":"transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:HGNC:29808]","synonyms":"TMPRSS11,MSPL","biotype":"protein_coding","ncbi_id":"84000","summary":"This gene encodes a member of the type II transmembrane serine protease family. Transmembrane serine proteases are regulated by protease inhibitors and known to function in development, homeostasis, infection, and tumorigenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":117900643,"end":117929459,"strand":-1,"description":"transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:HGNC:29808]"}, {"versioned_ensembl_gene_id":"ENSG00000270108.1","gene_symbol":"AL049840.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":103687576,"end":103688127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277769.1","gene_symbol":"RBM22P4","gene_name":"RNA binding motif protein 22 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271870","summary":null,"start":45098021,"end":45099260,"strand":1,"description":"RNA binding motif protein 22 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39697]"}, {"versioned_ensembl_gene_id":"ENSG00000284703.1","gene_symbol":"AL805961.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4012921,"end":4019508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284668.1","gene_symbol":"AL805961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3976133,"end":4012699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230226.1","gene_symbol":"AL121829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63502287,"end":63505111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264112.1","gene_symbol":"AC015813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57989039,"end":57994850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248491.5","gene_symbol":"AC093772.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127096891,"end":127470569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139865.16","gene_symbol":"TTC6","gene_name":"tetratricopeptide repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:19739]","synonyms":"NCRNA00291,C14orf25","biotype":"protein_coding","ncbi_id":"319089","summary":null,"start":37595847,"end":38041442,"strand":1,"description":"tetratricopeptide repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:19739]"}, {"versioned_ensembl_gene_id":"ENSG00000136451.8","gene_symbol":"VEZF1","gene_name":"vascular endothelial zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:12949]","synonyms":"ZNF161,DB1","biotype":"protein_coding","ncbi_id":"7716","summary":"Transcriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2-type zinc finger protein (Koyano-Nakagawa et al., 1994 [PubMed 8035792]). See MIM 603971 for general information on zinc finger proteins.[supplied by OMIM, Sep 2008]","start":57971547,"end":57988259,"strand":-1,"description":"vascular endothelial zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:12949]"}, {"versioned_ensembl_gene_id":"ENSG00000277549.1","gene_symbol":"AL359920.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60322591,"end":60322766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087206.16","gene_symbol":"UIMC1","gene_name":"ubiquitin interaction motif containing 1 [Source:HGNC Symbol;Acc:HGNC:30298]","synonyms":"RAP80","biotype":"protein_coding","ncbi_id":"51720","summary":"This gene encodes a nuclear protein that interacts with Brca1 (breast cancer 1) in a complex to recognize and repair DNA lesions. This protein binds ubiquitinated lysine 63 of histone H2A and H2AX. This protein may also function as a repressor of transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":176905005,"end":177022633,"strand":-1,"description":"ubiquitin interaction motif containing 1 [Source:HGNC Symbol;Acc:HGNC:30298]"}, {"versioned_ensembl_gene_id":"ENSG00000235571.1","gene_symbol":"SNX18P14","gene_name":"sorting nexin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418972","summary":null,"start":94786688,"end":94787261,"strand":-1,"description":"sorting nexin 18 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39622]"}, {"versioned_ensembl_gene_id":"ENSG00000271576.1","gene_symbol":"AL359504.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84076331,"end":84077931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259214.1","gene_symbol":"AC012414.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20826454,"end":20826640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137392.9","gene_symbol":"CLPS","gene_name":"colipase [Source:HGNC Symbol;Acc:HGNC:2085]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1208","summary":"The protein encoded by this gene is a cofactor needed by pancreatic lipase for efficient dietary lipid hydrolysis. It binds to the C-terminal, non-catalytic domain of lipase, thereby stabilizing an active conformation and considerably increasing the overall hydrophobic binding site. The gene product allows lipase to anchor noncovalently to the surface of lipid micelles, counteracting the destabilizing influence of intestinal bile salts. This cofactor is only expressed in pancreatic acinar cells, suggesting regulation of expression by tissue-specific elements. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":35794982,"end":35797344,"strand":-1,"description":"colipase [Source:HGNC Symbol;Acc:HGNC:2085]"}, {"versioned_ensembl_gene_id":"ENSG00000205572.9","gene_symbol":"SERF1B","gene_name":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]","synonyms":"H4F5C,FAM2B","biotype":"protein_coding","ncbi_id":"728492","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008]","start":70025247,"end":70043113,"strand":1,"description":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]"}, {"versioned_ensembl_gene_id":"ENSG00000276819.1","gene_symbol":"AC244472.4","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142592928,"end":142593473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213778.2","gene_symbol":"HNRNPA1P32","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:44958]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645940","summary":null,"start":30517616,"end":30518861,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:44958]"}, {"versioned_ensembl_gene_id":"ENSG00000145555.14","gene_symbol":"MYO10","gene_name":"myosin X [Source:HGNC Symbol;Acc:HGNC:7593]","synonyms":"KIAA0799","biotype":"protein_coding","ncbi_id":"4651","summary":"This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-10 (MYH10). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. This gene functions as an actin-based molecular motor and plays a role in integration of F-actin and microtubule cytoskeletons during meiosis. [provided by RefSeq, Dec 2011]","start":16661914,"end":16936276,"strand":-1,"description":"myosin X [Source:HGNC Symbol;Acc:HGNC:7593]"}, {"versioned_ensembl_gene_id":"ENSG00000275144.1","gene_symbol":"SNX18P5","gene_name":"sorting nexin 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39613]","synonyms":"SNX18P6","biotype":"unprocessed_pseudogene","ncbi_id":"100418977","summary":null,"start":42923277,"end":42924144,"strand":1,"description":"sorting nexin 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39613]"}, {"versioned_ensembl_gene_id":"ENSG00000197128.11","gene_symbol":"ZNF772","gene_name":"zinc finger protein 772 [Source:HGNC Symbol;Acc:HGNC:33106]","synonyms":"DKFZp686I1569","biotype":"protein_coding","ncbi_id":"400720","summary":null,"start":57466663,"end":57477570,"strand":-1,"description":"zinc finger protein 772 [Source:HGNC Symbol;Acc:HGNC:33106]"}, {"versioned_ensembl_gene_id":"ENSG00000251630.1","gene_symbol":"AC119751.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49561285,"end":49561470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108582.11","gene_symbol":"CPD","gene_name":"carboxypeptidase D [Source:HGNC Symbol;Acc:HGNC:2301]","synonyms":"GP180","biotype":"protein_coding","ncbi_id":"1362","summary":"The metallocarboxypeptidase family of enzymes is divided into 2 subfamilies based on sequence similarities. The pancreatic carboxypeptidase-like and the regulatory B-type carboxypeptidase subfamilies. Carboxypeptidase D has been identified as a regulatory B-type carboxypeptidase. CPD is a homolog of duck gp180, a hepatitis B virus-binding protein. Transcript variants utilizing alternative polyadenylation signals exist for this gene. [provided by RefSeq, Jul 2008]","start":30378905,"end":30469989,"strand":1,"description":"carboxypeptidase D [Source:HGNC Symbol;Acc:HGNC:2301]"}, {"versioned_ensembl_gene_id":"ENSG00000251649.1","gene_symbol":"LINC02379","gene_name":"long intergenic non-protein coding RNA 2379 [Source:HGNC Symbol;Acc:HGNC:53302]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927109","summary":null,"start":126070708,"end":126072004,"strand":1,"description":"long intergenic non-protein coding RNA 2379 [Source:HGNC Symbol;Acc:HGNC:53302]"}, {"versioned_ensembl_gene_id":"ENSG00000081237.18","gene_symbol":"PTPRC","gene_name":"protein tyrosine phosphatase, receptor type C [Source:HGNC Symbol;Acc:HGNC:9666]","synonyms":"T200,LCA,GP180,CD45","biotype":"protein_coding","ncbi_id":"5788","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitosis, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus is classified as a receptor type PTP. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling. Alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jun 2012]","start":198638671,"end":198757283,"strand":1,"description":"protein tyrosine phosphatase, receptor type C [Source:HGNC Symbol;Acc:HGNC:9666]"}, {"versioned_ensembl_gene_id":"ENSG00000234016.1","gene_symbol":"GNG10P1","gene_name":"G protein subunit gamma 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49502]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100526656","summary":null,"start":125960208,"end":125960406,"strand":-1,"description":"G protein subunit gamma 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49502]"}, {"versioned_ensembl_gene_id":"ENSG00000204140.9","gene_symbol":"CLPSL1","gene_name":"colipase like 1 [Source:HGNC Symbol;Acc:HGNC:21251]","synonyms":"dJ510O8.6,C6orf127","biotype":"protein_coding","ncbi_id":"340204","summary":null,"start":35781017,"end":35793675,"strand":1,"description":"colipase like 1 [Source:HGNC Symbol;Acc:HGNC:21251]"}, {"versioned_ensembl_gene_id":"ENSG00000180891.12","gene_symbol":"CUEDC1","gene_name":"CUE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:31350]","synonyms":null,"biotype":"protein_coding","ncbi_id":"404093","summary":null,"start":57861243,"end":57955323,"strand":-1,"description":"CUE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:31350]"}, {"versioned_ensembl_gene_id":"ENSG00000256925.2","gene_symbol":"ADGRA1-AS1","gene_name":"adhesion G protein-coupled receptor A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49543]","synonyms":"GPR123-AS1","biotype":"antisense_RNA","ncbi_id":"100128127","summary":null,"start":133083073,"end":133088491,"strand":-1,"description":"adhesion G protein-coupled receptor A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49543]"}, {"versioned_ensembl_gene_id":"ENSG00000264914.1","gene_symbol":"AC015845.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57912333,"end":57922581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217160.2","gene_symbol":"MTCO2P31","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52160]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075292","summary":null,"start":153665707,"end":153666390,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52160]"}, {"versioned_ensembl_gene_id":"ENSG00000181291.7","gene_symbol":"TMEM132E","gene_name":"transmembrane protein 132E [Source:HGNC Symbol;Acc:HGNC:26991]","synonyms":"DFNB99","biotype":"protein_coding","ncbi_id":"124842","summary":null,"start":34579487,"end":34639318,"strand":1,"description":"transmembrane protein 132E [Source:HGNC Symbol;Acc:HGNC:26991]"}, {"versioned_ensembl_gene_id":"ENSG00000275791.1","gene_symbol":"TRBV10-3","gene_name":"T-cell receptor beta variable 10-3 [Source:HGNC Symbol;Acc:HGNC:12179]","synonyms":"TCRBV12S1A1N2,TCRBV10S3,TRBV103","biotype":"TR_V_gene","ncbi_id":"28583","summary":null,"start":142544212,"end":142544685,"strand":1,"description":"T-cell receptor beta variable 10-3 [Source:HGNC Symbol;Acc:HGNC:12179]"}, {"versioned_ensembl_gene_id":"ENSG00000230815.1","gene_symbol":"AL807757.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":94824272,"end":94824773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260162.2","gene_symbol":"AC134312.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88177289,"end":88178646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188070.9","gene_symbol":"C11orf95","gene_name":"chromosome 11 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:28449]","synonyms":"MGC3032","biotype":"protein_coding","ncbi_id":"65998","summary":null,"start":63759892,"end":63768775,"strand":-1,"description":"chromosome 11 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:28449]"}, {"versioned_ensembl_gene_id":"ENSG00000258423.1","gene_symbol":"OR7E105P","gene_name":"olfactory receptor family 7 subfamily E member 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:15364]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81116","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":51756996,"end":51757988,"strand":1,"description":"olfactory receptor family 7 subfamily E member 105 pseudogene [Source:HGNC Symbol;Acc:HGNC:15364]"}, {"versioned_ensembl_gene_id":"ENSG00000227979.1","gene_symbol":"AC002127.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88749470,"end":88749694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163596.16","gene_symbol":"ICA1L","gene_name":"islet cell autoantigen 1 like [Source:HGNC Symbol;Acc:HGNC:14442]","synonyms":"ALS2CR15,ALS2CR14","biotype":"protein_coding","ncbi_id":"130026","summary":null,"start":202773150,"end":202871985,"strand":-1,"description":"islet cell autoantigen 1 like [Source:HGNC Symbol;Acc:HGNC:14442]"}, {"versioned_ensembl_gene_id":"ENSG00000259251.2","gene_symbol":"AC104590.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62060503,"end":62062434,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007944.14","gene_symbol":"MYLIP","gene_name":"myosin regulatory light chain interacting protein [Source:HGNC Symbol;Acc:HGNC:21155]","synonyms":"MIR,IDOL","biotype":"protein_coding","ncbi_id":"29116","summary":"The ERM protein family members ezrin, radixin, and moesin are cytoskeletal effector proteins linking actin to membrane-bound proteins at the cell surface. Myosin regulatory light chain interacting protein (MYLIP) is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth. [provided by RefSeq, Jul 2008]","start":16129125,"end":16148248,"strand":1,"description":"myosin regulatory light chain interacting protein [Source:HGNC Symbol;Acc:HGNC:21155]"}, {"versioned_ensembl_gene_id":"ENSG00000156804.7","gene_symbol":"FBXO32","gene_name":"F-box protein 32 [Source:HGNC Symbol;Acc:HGNC:16731]","synonyms":"MAFbx,Fbx32,ATROGIN1","biotype":"protein_coding","ncbi_id":"114907","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and contains an F-box domain. This protein is highly expressed during muscle atrophy, whereas mice deficient in this gene were found to be resistant to atrophy. This protein is thus a potential drug target for the treatment of muscle atrophy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]","start":123497889,"end":123541206,"strand":-1,"description":"F-box protein 32 [Source:HGNC Symbol;Acc:HGNC:16731]"}, {"versioned_ensembl_gene_id":"ENSG00000179526.16","gene_symbol":"SHARPIN","gene_name":"SHANK associated RH domain interactor [Source:HGNC Symbol;Acc:HGNC:25321]","synonyms":"SIPL1,DKFZP434N1923","biotype":"protein_coding","ncbi_id":"81858","summary":null,"start":144098633,"end":144108124,"strand":-1,"description":"SHANK associated RH domain interactor [Source:HGNC Symbol;Acc:HGNC:25321]"}, {"versioned_ensembl_gene_id":"ENSG00000275333.4","gene_symbol":"FAM120B","gene_name":"family with sequence similarity 120B [Source:HGNC Symbol;Acc:HGNC:21109]","synonyms":"PGCC1,KIAA1838,CCPG","biotype":"protein_coding","ncbi_id":"84498","summary":null,"start":170290703,"end":170416388,"strand":1,"description":"family with sequence similarity 120B [Source:HGNC Symbol;Acc:HGNC:21109]"}, {"versioned_ensembl_gene_id":"ENSG00000235653.1","gene_symbol":"AC007253.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39929110,"end":39929998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264145.2","gene_symbol":"AC239859.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143449571,"end":143450245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277949.2","gene_symbol":"RTP5","gene_name":"receptor transporter protein 5 (putative) [Source:HGNC Symbol;Acc:HGNC:26585]","synonyms":"CXXC11,C2orf85,Z3CXXC5,FLJ33590","biotype":"protein_coding","ncbi_id":"285093","summary":null,"start":241869600,"end":241873823,"strand":1,"description":"receptor transporter protein 5 (putative) [Source:HGNC Symbol;Acc:HGNC:26585]"}, {"versioned_ensembl_gene_id":"ENSG00000277702.1","gene_symbol":"AC239859.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143419625,"end":143420207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269954.1","gene_symbol":"AC022239.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11552488,"end":11552991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223815.1","gene_symbol":"DIAPH3-AS2","gene_name":"DIAPH3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39916]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874196","summary":null,"start":60144698,"end":60153505,"strand":1,"description":"DIAPH3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39916]"}, {"versioned_ensembl_gene_id":"ENSG00000260265.1","gene_symbol":"LINC02562","gene_name":"long intergenic non-protein coding RNA 2562 [Source:HGNC Symbol;Acc:HGNC:53602]","synonyms":"RP11-44F21.5","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75081702,"end":75084717,"strand":-1,"description":"long intergenic non-protein coding RNA 2562 [Source:HGNC Symbol;Acc:HGNC:53602]"}, {"versioned_ensembl_gene_id":"ENSG00000253825.1","gene_symbol":"AC097173.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120035033,"end":120040615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242088.1","gene_symbol":"AC090602.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24910874,"end":24911125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233423.1","gene_symbol":"AC005482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67691058,"end":67697029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271475.1","gene_symbol":"AL078624.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":228776312,"end":228776865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250448.1","gene_symbol":"AC092335.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16180238,"end":16185585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279286.2","gene_symbol":"AL133373.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":91572444,"end":91575271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250981.1","gene_symbol":"AC016650.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16129178,"end":16141602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282679.1","gene_symbol":"IGHV3-71","gene_name":"immunoglobulin heavy variable 3-71 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5621]","synonyms":"IGHV3-G","biotype":"IG_V_pseudogene","ncbi_id":"28411","summary":null,"start":106799336,"end":106799794,"strand":-1,"description":"immunoglobulin heavy variable 3-71 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5621]"}, {"versioned_ensembl_gene_id":"ENSG00000237437.1","gene_symbol":"ASS1P12","gene_name":"argininosuccinate synthetase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:762]","synonyms":"ASSP12","biotype":"processed_pseudogene","ncbi_id":"392302","summary":null,"start":32945996,"end":32947222,"strand":1,"description":"argininosuccinate synthetase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:762]"}, {"versioned_ensembl_gene_id":"ENSG00000236796.1","gene_symbol":"AL157884.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32836575,"end":32869595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143537.13","gene_symbol":"ADAM15","gene_name":"ADAM metallopeptidase domain 15 [Source:HGNC Symbol;Acc:HGNC:193]","synonyms":"MDC15","biotype":"protein_coding","ncbi_id":"8751","summary":"The protein encoded by this gene is a member of the ADAM (a disintegrin and metalloproteinase) protein family. ADAM family members are type I transmembrane glycoproteins known to be involved in cell adhesion and proteolytic ectodomain processing of cytokines and adhesion molecules. This protein contains multiple functional domains including a zinc-binding metalloprotease domain, a disintegrin-like domain, as well as a EGF-like domain. Through its disintegrin-like domain, this protein specifically interacts with the integrin beta chain, beta 3. It also interacts with Src family protein-tyrosine kinases in a phosphorylation-dependent manner, suggesting that this protein may function in cell-cell adhesion as well as in cellular signaling. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":155050566,"end":155062775,"strand":1,"description":"ADAM metallopeptidase domain 15 [Source:HGNC Symbol;Acc:HGNC:193]"}, {"versioned_ensembl_gene_id":"ENSG00000249079.1","gene_symbol":"AC118282.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49212251,"end":49212624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282421.1","gene_symbol":"AC245369.5","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106752844,"end":106753288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275148.2","gene_symbol":"AC245369.2","gene_name":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106761791,"end":106762228,"strand":-1,"description":"Immunoglobulin heavy variable 1-69-2 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JMI3]"}, {"versioned_ensembl_gene_id":"ENSG00000237442.3","gene_symbol":"HNRNPA1P57","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:48787]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"101060039","summary":null,"start":41143780,"end":41157555,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:48787]"}, {"versioned_ensembl_gene_id":"ENSG00000123338.12","gene_symbol":"NCKAP1L","gene_name":"NCK associated protein 1 like [Source:HGNC Symbol;Acc:HGNC:4862]","synonyms":"HEM1","biotype":"protein_coding","ncbi_id":"3071","summary":"This gene encodes a member of the HEM family of tissue-specific transmembrane proteins which are highly conserved from invertebrates through mammals. This gene is only expressed in hematopoietic cells. The encoded protein is a part of the Scar/WAVE complex which plays an important role in regulating cell shape in both metazoans and plants. Alternatively spliced transcript variants encoding different isoforms have been found.[provided by RefSeq, May 2010]","start":54497711,"end":54548238,"strand":1,"description":"NCK associated protein 1 like [Source:HGNC Symbol;Acc:HGNC:4862]"}, {"versioned_ensembl_gene_id":"ENSG00000257824.1","gene_symbol":"AC068789.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54543111,"end":54544105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260338.1","gene_symbol":"LINC01570","gene_name":"long intergenic non-protein coding RNA 1570 [Source:HGNC Symbol;Acc:HGNC:51382]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926950","summary":null,"start":5601169,"end":5616196,"strand":-1,"description":"long intergenic non-protein coding RNA 1570 [Source:HGNC Symbol;Acc:HGNC:51382]"}, {"versioned_ensembl_gene_id":"ENSG00000272189.1","gene_symbol":"AL024508.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136550661,"end":136552554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172845.14","gene_symbol":"SP3","gene_name":"Sp3 transcription factor [Source:HGNC Symbol;Acc:HGNC:11208]","synonyms":"SPR-2","biotype":"protein_coding","ncbi_id":"6670","summary":"This gene belongs to a family of Sp1 related genes that encode transcription factors that regulate transcription by binding to consensus GC- and GT-box regulatory elements in target genes. This protein contains a zinc finger DNA-binding domain and several transactivation domains, and has been reported to function as a bifunctional transcription factor that either stimulates or represses the transcription of numerous genes. Transcript variants encoding different isoforms have been described for this gene, and one has been reported to initiate translation from a non-AUG (AUA) start codon. Additional isoforms, resulting from the use of alternate downstream translation initiation sites, have also been noted. A related pseudogene has been identified on chromosome 13. [provided by RefSeq, Feb 2010]","start":173906459,"end":173965702,"strand":-1,"description":"Sp3 transcription factor [Source:HGNC Symbol;Acc:HGNC:11208]"}, {"versioned_ensembl_gene_id":"ENSG00000162931.11","gene_symbol":"TRIM17","gene_name":"tripartite motif containing 17 [Source:HGNC Symbol;Acc:HGNC:13430]","synonyms":"terf,RNF16,RBCC","biotype":"protein_coding","ncbi_id":"51127","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. The protein is expressed almost exclusively in the testis, but its function is unknown. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":228407940,"end":228416861,"strand":-1,"description":"tripartite motif containing 17 [Source:HGNC Symbol;Acc:HGNC:13430]"}, {"versioned_ensembl_gene_id":"ENSG00000268182.5","gene_symbol":"SMIM17","gene_name":"small integral membrane protein 17 [Source:HGNC Symbol;Acc:HGNC:27114]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147670","summary":null,"start":56643145,"end":56655766,"strand":1,"description":"small integral membrane protein 17 [Source:HGNC Symbol;Acc:HGNC:27114]"}, {"versioned_ensembl_gene_id":"ENSG00000255148.2","gene_symbol":"AC239802.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149018671,"end":149026269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274031.1","gene_symbol":"AC092140.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56465642,"end":56466162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127903.13","gene_symbol":"ZNF835","gene_name":"zinc finger protein 835 [Source:HGNC Symbol;Acc:HGNC:34332]","synonyms":"BC37295_3","biotype":"protein_coding","ncbi_id":"90485","summary":null,"start":56661981,"end":56671783,"strand":-1,"description":"zinc finger protein 835 [Source:HGNC Symbol;Acc:HGNC:34332]"}, {"versioned_ensembl_gene_id":"ENSG00000254913.1","gene_symbol":"AC239802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149006309,"end":149009527,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258924.4","gene_symbol":"AC002094.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28357647,"end":28381697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283031.1","gene_symbol":"AC009242.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23667208,"end":23685453,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224361.1","gene_symbol":"AC011239.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23507043,"end":23524344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274529.5","gene_symbol":"SEBOX","gene_name":"SEBOX homeobox [Source:HGNC Symbol;Acc:HGNC:32942]","synonyms":"OG9X,OG9","biotype":"protein_coding","ncbi_id":"645832","summary":"Homeodomain proteins, such as SEBOX, play a key role in coordinating gene expression during development (Cinquanta et al., 2000 [PubMed 10922053]).[supplied by OMIM, Mar 2008]","start":28364268,"end":28365244,"strand":-1,"description":"SEBOX homeobox [Source:HGNC Symbol;Acc:HGNC:32942]"}, {"versioned_ensembl_gene_id":"ENSG00000268352.1","gene_symbol":"AC006115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56672268,"end":56684653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268568.1","gene_symbol":"AC007228.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56672574,"end":56673901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225520.1","gene_symbol":"TTTY16","gene_name":"testis-specific transcript, Y-linked 16 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18840]","synonyms":"NCRNA00139","biotype":"lincRNA","ncbi_id":"252948","summary":null,"start":7699357,"end":7701247,"strand":-1,"description":"testis-specific transcript, Y-linked 16 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18840]"}, {"versioned_ensembl_gene_id":"ENSG00000181016.9","gene_symbol":"LSMEM1","gene_name":"leucine rich single-pass membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:22036]","synonyms":"FLJ39575,C7orf53","biotype":"protein_coding","ncbi_id":"286006","summary":null,"start":112480853,"end":112491062,"strand":1,"description":"leucine rich single-pass membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:22036]"}, {"versioned_ensembl_gene_id":"ENSG00000216519.2","gene_symbol":"AL023284.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136317961,"end":136318236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258761.1","gene_symbol":"AC116903.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92162798,"end":92172436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089847.12","gene_symbol":"ANKRD24","gene_name":"ankyrin repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:29424]","synonyms":"KIAA1981","biotype":"protein_coding","ncbi_id":"170961","summary":null,"start":4183354,"end":4224814,"strand":1,"description":"ankyrin repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:29424]"}, {"versioned_ensembl_gene_id":"ENSG00000282309.1","gene_symbol":"AC093627.14","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177241,"end":178334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234069.1","gene_symbol":"GAPDHP53","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38559]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421318","summary":null,"start":24445391,"end":24446314,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38559]"}, {"versioned_ensembl_gene_id":"ENSG00000211706.2","gene_symbol":"TRBV6-1","gene_name":"T-cell receptor beta variable 6-1 [Source:HGNC Symbol;Acc:HGNC:12226]","synonyms":"TRBV61,TCRBV6S1,TCRBV13S3","biotype":"TR_V_gene","ncbi_id":"28606","summary":null,"start":142328297,"end":142328786,"strand":1,"description":"T-cell receptor beta variable 6-1 [Source:HGNC Symbol;Acc:HGNC:12226]"}, {"versioned_ensembl_gene_id":"ENSG00000237936.1","gene_symbol":"AL353093.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29891032,"end":29891467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211707.3","gene_symbol":"TRBV7-1","gene_name":"T-cell receptor beta variable 7-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12235]","synonyms":"TRBV71,TCRBV7S1,TCRBV6S7P","biotype":"TR_V_gene","ncbi_id":"28597","summary":null,"start":142332182,"end":142332701,"strand":1,"description":"T-cell receptor beta variable 7-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12235]"}, {"versioned_ensembl_gene_id":"ENSG00000219355.2","gene_symbol":"RPL31P52","gene_name":"ribosomal protein L31 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36607]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271476","summary":null,"start":120450437,"end":120450803,"strand":-1,"description":"ribosomal protein L31 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:36607]"}, {"versioned_ensembl_gene_id":"ENSG00000111786.8","gene_symbol":"SRSF9","gene_name":"serine and arginine rich splicing factor 9 [Source:HGNC Symbol;Acc:HGNC:10791]","synonyms":"SRp30c,SFRS9","biotype":"protein_coding","ncbi_id":"8683","summary":"The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two pseudogenes, one on chromosome 15 and the other on chromosome 21, have been found for this gene. [provided by RefSeq, Sep 2010]","start":120461668,"end":120469793,"strand":-1,"description":"serine and arginine rich splicing factor 9 [Source:HGNC Symbol;Acc:HGNC:10791]"}, {"versioned_ensembl_gene_id":"ENSG00000100796.17","gene_symbol":"PPP4R3A","gene_name":"protein phosphatase 4 regulatory subunit 3A [Source:HGNC Symbol;Acc:HGNC:20219]","synonyms":"smk1,smk-1,SMEK1,PP4R3,MSTP033,KIAA2010,FLJ20707,FLFL1","biotype":"protein_coding","ncbi_id":"55671","summary":null,"start":91457611,"end":91510554,"strand":-1,"description":"protein phosphatase 4 regulatory subunit 3A [Source:HGNC Symbol;Acc:HGNC:20219]"}, {"versioned_ensembl_gene_id":"ENSG00000258420.1","gene_symbol":"AC012414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20775464,"end":20775998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174808.11","gene_symbol":"BTC","gene_name":"betacellulin [Source:HGNC Symbol;Acc:HGNC:1121]","synonyms":null,"biotype":"protein_coding","ncbi_id":"685","summary":"This gene encodes a member of the epidermal growth factor (EGF) family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the secreted growth factor. A secreted form and a membrane-anchored form of this protein bind to multiple different EGF receptors. This protein promotes pancreatic cell proliferation and insulin secretion, as well as retinal vascular permeability. Mutations in this gene may be associated with type 2 diabetes in human patients. [provided by RefSeq, Nov 2015]","start":74744759,"end":74794686,"strand":-1,"description":"betacellulin [Source:HGNC Symbol;Acc:HGNC:1121]"}, {"versioned_ensembl_gene_id":"ENSG00000181315.10","gene_symbol":"ZNF322","gene_name":"zinc finger protein 322 [Source:HGNC Symbol;Acc:HGNC:23640]","synonyms":"ZNF388,ZNF322A,HCG12,bA457M11.3,bA457M11.2,ZNF489","biotype":"protein_coding","ncbi_id":"79692","summary":"ZNF322A is a member of the zinc-finger transcription factor family and may regulate transcriptional activation in MAPK (see MAPK1; MIM 176948) signaling pathways (Li et al., 2004 [PubMed 15555580]).[supplied by OMIM, Mar 2008]","start":26634383,"end":26659752,"strand":-1,"description":"zinc finger protein 322 [Source:HGNC Symbol;Acc:HGNC:23640]"}, {"versioned_ensembl_gene_id":"ENSG00000228333.9","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"H-2RIIBP,RCoR-1,NR2B2","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33171494,"end":33178594,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000282575.1","gene_symbol":"AC093627.18","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185256,"end":196501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145375.7","gene_symbol":"SPATA5","gene_name":"spermatogenesis associated 5 [Source:HGNC Symbol;Acc:HGNC:18119]","synonyms":"SPAF,AFG2","biotype":"protein_coding","ncbi_id":"166378","summary":"This gene encodes a member of the ATPase associated with diverse activities family, whose members are defined by a highly conserved ATPase domain. Members of this family participate in diverse cellular processes that include membrane fusion, DNA replication, microtubule severing, and protein degradation. The protein encoded by this gene has a putative mitochondrial targeting sequence and has been proposed to function in maintenance of mitochondrial function and integrity during mouse spermatogenesis. Allelic variants in this gene have been associated with epilepsy, hearing loss, and cognitive disability syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":122923074,"end":123319450,"strand":1,"description":"spermatogenesis associated 5 [Source:HGNC Symbol;Acc:HGNC:18119]"}, {"versioned_ensembl_gene_id":"ENSG00000231086.1","gene_symbol":"TSSK1A","gene_name":"testis specific serine kinase 1A, pseudogene [Source:HGNC Symbol;Acc:HGNC:11400]","synonyms":"TSSK7P,TSSK1AP,TSSK1,STK22A,SPOGA1","biotype":"unitary_pseudogene","ncbi_id":"23752","summary":null,"start":19124879,"end":19125646,"strand":1,"description":"testis specific serine kinase 1A, pseudogene [Source:HGNC Symbol;Acc:HGNC:11400]"}, {"versioned_ensembl_gene_id":"ENSG00000175514.2","gene_symbol":"GPR152","gene_name":"G protein-coupled receptor 152 [Source:HGNC Symbol;Acc:HGNC:23622]","synonyms":"PGR5","biotype":"protein_coding","ncbi_id":"390212","summary":null,"start":67451301,"end":67452729,"strand":-1,"description":"G protein-coupled receptor 152 [Source:HGNC Symbol;Acc:HGNC:23622]"}, {"versioned_ensembl_gene_id":"ENSG00000282147.1","gene_symbol":"FAM20C","gene_name":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]","synonyms":"IMAGE:4942737,G-CK,DMP4,DKFZp547D065","biotype":"protein_coding","ncbi_id":"56975","summary":"This gene encodes a member of the family of secreted protein kinases. The encoded protein binds calcium and phosphorylates proteins involved in bone mineralization. Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Apr 2014]","start":195290,"end":199896,"strand":1,"description":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]"}, {"versioned_ensembl_gene_id":"ENSG00000237347.2","gene_symbol":"AC004461.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19055801,"end":19056512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281530.1","gene_symbol":"AC004461.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19061041,"end":19061843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175544.13","gene_symbol":"CABP4","gene_name":"calcium binding protein 4 [Source:HGNC Symbol;Acc:HGNC:1386]","synonyms":"CSNB2B","biotype":"protein_coding","ncbi_id":"57010","summary":"This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":67452406,"end":67460313,"strand":1,"description":"calcium binding protein 4 [Source:HGNC Symbol;Acc:HGNC:1386]"}, {"versioned_ensembl_gene_id":"ENSG00000273311.1","gene_symbol":"DGCR11","gene_name":"DiGeorge syndrome critical region gene 11 (non-protein coding) [Source:NCBI gene;Acc:25786]","synonyms":"DGS-D","biotype":"sense_intronic","ncbi_id":"25786","summary":null,"start":19046162,"end":19048375,"strand":-1,"description":"DiGeorge syndrome critical region gene 11 (non-protein coding) [Source:NCBI gene;Acc:25786]"}, {"versioned_ensembl_gene_id":"ENSG00000175352.10","gene_symbol":"NRIP3","gene_name":"nuclear receptor interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:1167]","synonyms":"C11orf14","biotype":"protein_coding","ncbi_id":"56675","summary":null,"start":8980576,"end":9004049,"strand":-1,"description":"nuclear receptor interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:1167]"}, {"versioned_ensembl_gene_id":"ENSG00000272583.1","gene_symbol":"AL592494.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121518366,"end":121518829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070413.19","gene_symbol":"DGCR2","gene_name":"DiGeorge syndrome critical region gene 2 [Source:HGNC Symbol;Acc:HGNC:2845]","synonyms":"DGS-C,SEZ-12,LAN,KIAA0163,IDD","biotype":"protein_coding","ncbi_id":"9993","summary":"Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":19036282,"end":19122454,"strand":-1,"description":"DiGeorge syndrome critical region gene 2 [Source:HGNC Symbol;Acc:HGNC:2845]"}, {"versioned_ensembl_gene_id":"ENSG00000257218.5","gene_symbol":"GATC","gene_name":"glutamyl-tRNA amidotransferase subunit C [Source:HGNC Symbol;Acc:HGNC:25068]","synonyms":"gatC,FLJ37000,15E1.2","biotype":"protein_coding","ncbi_id":"283459","summary":null,"start":120446438,"end":120463749,"strand":1,"description":"glutamyl-tRNA amidotransferase subunit C [Source:HGNC Symbol;Acc:HGNC:25068]"}, {"versioned_ensembl_gene_id":"ENSG00000231752.5","gene_symbol":"EMBP1","gene_name":"embigin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38661]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"647121","summary":null,"start":121519112,"end":121571892,"strand":1,"description":"embigin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38661]"}, {"versioned_ensembl_gene_id":"ENSG00000262408.1","gene_symbol":"AC015912.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56884639,"end":56884819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224857.1","gene_symbol":"LINC01691","gene_name":"long intergenic non-protein coding RNA 1691 [Source:HGNC Symbol;Acc:HGNC:52479]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985195","summary":null,"start":121573946,"end":121580524,"strand":-1,"description":"long intergenic non-protein coding RNA 1691 [Source:HGNC Symbol;Acc:HGNC:52479]"}, {"versioned_ensembl_gene_id":"ENSG00000228827.1","gene_symbol":"AL929410.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51903338,"end":51903850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211745.3","gene_symbol":"TRBV4-2","gene_name":"T-cell receptor beta variable 4-2 [Source:HGNC Symbol;Acc:HGNC:12216]","synonyms":"TRBV42,TCRBV7S3A2T,TCRBV4S2","biotype":"TR_V_gene","ncbi_id":"28616","summary":null,"start":142345421,"end":142345985,"strand":1,"description":"T-cell receptor beta variable 4-2 [Source:HGNC Symbol;Acc:HGNC:12216]"}, {"versioned_ensembl_gene_id":"ENSG00000203880.11","gene_symbol":"PCMTD2","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15882]","synonyms":"FLJ10883,C20orf36","biotype":"protein_coding","ncbi_id":"55251","summary":null,"start":64255695,"end":64287821,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:15882]"}, {"versioned_ensembl_gene_id":"ENSG00000198300.12","gene_symbol":"PEG3","gene_name":"paternally expressed 3 [Source:HGNC Symbol;Acc:HGNC:8826]","synonyms":"ZSCAN24,ZNF904,ZKSCAN22,KIAA0287","biotype":"protein_coding","ncbi_id":"5178","summary":"In human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5' exons and a common promoter and both genes are paternally expressed (PMID:15203203). Alternative splicing events connect their shared 5' exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. In contrast, in other mammals ZIM2 does not undergo imprinting and, in mouse, cow, and likely other mammals as well, the ZIM2 and PEG3 genes do not share exons. Human PEG3 protein belongs to the Kruppel C2H2-type zinc finger protein family. PEG3 may play a role in cell proliferation and p53-mediated apoptosis. PEG3 has also shown tumor suppressor activity and tumorigenesis in glioma and ovarian cells. Alternative splicing of this PEG3 gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Sep 2009]","start":56810083,"end":56840728,"strand":-1,"description":"paternally expressed 3 [Source:HGNC Symbol;Acc:HGNC:8826]"}, {"versioned_ensembl_gene_id":"ENSG00000232951.1","gene_symbol":"IPO7P1","gene_name":"importin 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39837]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129708","summary":null,"start":51921864,"end":51922499,"strand":-1,"description":"importin 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39837]"}, {"versioned_ensembl_gene_id":"ENSG00000139263.11","gene_symbol":"LRIG3","gene_name":"leucine rich repeats and immunoglobulin like domains 3 [Source:HGNC Symbol;Acc:HGNC:30991]","synonyms":"KIAA3016,FLJ90440","biotype":"protein_coding","ncbi_id":"121227","summary":null,"start":58872149,"end":58920522,"strand":-1,"description":"leucine rich repeats and immunoglobulin like domains 3 [Source:HGNC Symbol;Acc:HGNC:30991]"}, {"versioned_ensembl_gene_id":"ENSG00000262112.1","gene_symbol":"AC015912.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56888880,"end":56891841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237528.1","gene_symbol":"AL929410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51923552,"end":51923740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250322.2","gene_symbol":"AC026402.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123259949,"end":123260118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237156.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30623868,"end":30624134,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000121060.16","gene_symbol":"TRIM25","gene_name":"tripartite motif containing 25 [Source:HGNC Symbol;Acc:HGNC:12932]","synonyms":"ZNF147,RNF147,EFP","biotype":"protein_coding","ncbi_id":"7706","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. The presence of potential DNA-binding and dimerization-transactivation domains suggests that this protein may act as a transcription factor, similar to several other members of the TRIM family. Expression of the gene is upregulated in response to estrogen, and it is thought to mediate estrogen actions in breast cancer as a primary response gene. [provided by RefSeq, Jul 2008]","start":56887909,"end":56914038,"strand":-1,"description":"tripartite motif containing 25 [Source:HGNC Symbol;Acc:HGNC:12932]"}, {"versioned_ensembl_gene_id":"ENSG00000172663.8","gene_symbol":"TMEM134","gene_name":"transmembrane protein 134 [Source:HGNC Symbol;Acc:HGNC:26142]","synonyms":"FLJ21749","biotype":"protein_coding","ncbi_id":"80194","summary":null,"start":67461710,"end":67469272,"strand":-1,"description":"transmembrane protein 134 [Source:HGNC Symbol;Acc:HGNC:26142]"}, {"versioned_ensembl_gene_id":"ENSG00000111780.8","gene_symbol":"AL021546.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":120438198,"end":120460006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232562.1","gene_symbol":"TPMTP3","gene_name":"thiopurine S-methyltransferase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44566]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129277","summary":null,"start":51979223,"end":51980012,"strand":-1,"description":"thiopurine S-methyltransferase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44566]"}, {"versioned_ensembl_gene_id":"ENSG00000228539.1","gene_symbol":"AL157413.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24491472,"end":24502345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257771.5","gene_symbol":"LINC02395","gene_name":"long intergenic non-protein coding RNA 2395 [Source:HGNC Symbol;Acc:HGNC:53322]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927292","summary":null,"start":49911953,"end":49930320,"strand":1,"description":"long intergenic non-protein coding RNA 2395 [Source:HGNC Symbol;Acc:HGNC:53322]"}, {"versioned_ensembl_gene_id":"ENSG00000170855.3","gene_symbol":"TRIAP1","gene_name":"TP53 regulated inhibitor of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:26937]","synonyms":"WF-1,P53CSV,MDM35,HSPC132","biotype":"protein_coding","ncbi_id":"51499","summary":null,"start":120443961,"end":120446412,"strand":-1,"description":"TP53 regulated inhibitor of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:26937]"}, {"versioned_ensembl_gene_id":"ENSG00000101463.5","gene_symbol":"SYNDIG1","gene_name":"synapse differentiation inducing 1 [Source:HGNC Symbol;Acc:HGNC:15885]","synonyms":"TMEM90B,SynDIG1,IFITMD5,FLJ14220,C20orf39","biotype":"protein_coding","ncbi_id":"79953","summary":"This gene encodes a protein that belongs to the interferon-induced transmembrane family of proteins. A similar protein in rat is thought to regulate the development of excitatory synapses. [provided by RefSeq, Jul 2013]","start":24469199,"end":24666616,"strand":1,"description":"synapse differentiation inducing 1 [Source:HGNC Symbol;Acc:HGNC:15885]"}, {"versioned_ensembl_gene_id":"ENSG00000182776.4","gene_symbol":"AC239585.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52050860,"end":52054255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278057.4","gene_symbol":"TEX28","gene_name":"testis expressed 28 [Source:HGNC Symbol;Acc:HGNC:2563]","synonyms":"fTEX,CXorf2","biotype":"protein_coding","ncbi_id":"1527","summary":null,"start":154271265,"end":154295853,"strand":-1,"description":"testis expressed 28 [Source:HGNC Symbol;Acc:HGNC:2563]"}, {"versioned_ensembl_gene_id":"ENSG00000204315.3","gene_symbol":"FKBPL","gene_name":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]","synonyms":"NG7,DIR1,WISp39","biotype":"protein_coding","ncbi_id":"63943","summary":"The protein encoded by this gene has similarity to the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The encoded protein is thought to have a potential role in the induced radioresistance. Also it appears to have some involvement in the control of the cell cycle. [provided by RefSeq, Jul 2008]","start":32128707,"end":32130291,"strand":-1,"description":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]"}, {"versioned_ensembl_gene_id":"ENSG00000279750.3","gene_symbol":"AC239585.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52053176,"end":52055684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100239.15","gene_symbol":"PPP6R2","gene_name":"protein phosphatase 6 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:19253]","synonyms":"SAP190,KIAA0685,dJ579N16.1,SAPS2","biotype":"protein_coding","ncbi_id":"9701","summary":"The protein encoded by this gene is a regulatory protein for the protein phosphatase-6 catalytic subunit. Together, these proteins act as a significant T-loop phosphatase for Aurora A, an essential mitotic kinase. Loss of function of either the regulatory or catalytic subunit of protein phosphatase-6 interferes with spindle formation and chromosome alignment. [provided by RefSeq, May 2017]","start":50343304,"end":50445090,"strand":1,"description":"protein phosphatase 6 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:19253]"}, {"versioned_ensembl_gene_id":"ENSG00000262892.1","gene_symbol":"AC013759.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50465102,"end":50466010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111775.2","gene_symbol":"COX6A1","gene_name":"cytochrome c oxidase subunit 6A1 [Source:HGNC Symbol;Acc:HGNC:2277]","synonyms":"COX6A","biotype":"protein_coding","ncbi_id":"1337","summary":"Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in the electron transfer and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 1 (liver isoform) of subunit VIa, and polypeptide 1 is found in all non-muscle tissues. Polypeptide 2 (heart/muscle isoform) of subunit VIa is encoded by a different gene, and is present only in striated muscles. These two polypeptides share 66% amino acid sequence identity. It has been reported that there may be several pseudogenes on chromosomes 1, 6, 7q21, 7q31-32 and 12. However, only one pseudogene (COX6A1P) on chromosome 1p31.1 has been documented. [provided by RefSeq, Jul 2008]","start":120438090,"end":120440742,"strand":1,"description":"cytochrome c oxidase subunit 6A1 [Source:HGNC Symbol;Acc:HGNC:2277]"}, {"versioned_ensembl_gene_id":"ENSG00000283444.1","gene_symbol":"AC083865.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":37796058,"end":37796888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175414.6","gene_symbol":"ARL10","gene_name":"ADP ribosylation factor like GTPase 10 [Source:HGNC Symbol;Acc:HGNC:22042]","synonyms":"ARL10A","biotype":"protein_coding","ncbi_id":"285598","summary":null,"start":176365468,"end":176401865,"strand":1,"description":"ADP ribosylation factor like GTPase 10 [Source:HGNC Symbol;Acc:HGNC:22042]"}, {"versioned_ensembl_gene_id":"ENSG00000282110.1","gene_symbol":"MAPK4","gene_name":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]","synonyms":"Erk3-related,PRKM4,Erk4","biotype":"processed_transcript","ncbi_id":"5596","summary":"Mitogen-activated protein kinase 4 is a member of the mitogen-activated protein kinase family. Tyrosine kinase growth factor receptors activate mitogen-activated protein kinases which then translocate into the nucleus and phosphorylate nuclear targets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":50567310,"end":50567991,"strand":1,"description":"mitogen-activated protein kinase 4 [Source:HGNC Symbol;Acc:HGNC:6878]"}, {"versioned_ensembl_gene_id":"ENSG00000180934.6","gene_symbol":"OR56A1","gene_name":"olfactory receptor family 56 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14781]","synonyms":null,"biotype":"protein_coding","ncbi_id":"120796","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6019336,"end":6034338,"strand":-1,"description":"olfactory receptor family 56 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14781]"}, {"versioned_ensembl_gene_id":"ENSG00000229809.8","gene_symbol":"ZNF688","gene_name":"zinc finger protein 688 [Source:HGNC Symbol;Acc:HGNC:30489]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146542","summary":null,"start":30569346,"end":30572734,"strand":-1,"description":"zinc finger protein 688 [Source:HGNC Symbol;Acc:HGNC:30489]"}, {"versioned_ensembl_gene_id":"ENSG00000282433.1","gene_symbol":"AC012572.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78505165,"end":78506451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180019.5","gene_symbol":"AC079741.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112446164,"end":112446375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147649.9","gene_symbol":"MTDH","gene_name":"metadherin [Source:HGNC Symbol;Acc:HGNC:29608]","synonyms":"LYRIC,AEG-1,3D3","biotype":"protein_coding","ncbi_id":"92140","summary":null,"start":97644179,"end":97728770,"strand":1,"description":"metadherin [Source:HGNC Symbol;Acc:HGNC:29608]"}, {"versioned_ensembl_gene_id":"ENSG00000282429.1","gene_symbol":"AC208322.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51687527,"end":51688210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224237.1","gene_symbol":"MINOS1P3","gene_name":"mitochondrial inner membrane organizing system 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44093]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462954","summary":null,"start":27214816,"end":27215018,"strand":-1,"description":"mitochondrial inner membrane organizing system 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44093]"}, {"versioned_ensembl_gene_id":"ENSG00000171444.17","gene_symbol":"MCC","gene_name":"mutated in colorectal cancers [Source:HGNC Symbol;Acc:HGNC:6935]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4163","summary":"This gene is a candidate colorectal tumor suppressor gene that is thought to negatively regulate cell cycle progression. The orthologous gene in the mouse expresses a phosphoprotein associated with the plasma membrane and membrane organelles, and overexpression of the mouse protein inhibits entry into S phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":113022099,"end":113488830,"strand":-1,"description":"mutated in colorectal cancers [Source:HGNC Symbol;Acc:HGNC:6935]"}, {"versioned_ensembl_gene_id":"ENSG00000178503.6","gene_symbol":"NECAP1P1","gene_name":"NECAP endocytosis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43912]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442668","summary":null,"start":37585500,"end":37586329,"strand":-1,"description":"NECAP endocytosis associated 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43912]"}, {"versioned_ensembl_gene_id":"ENSG00000079156.16","gene_symbol":"OSBPL6","gene_name":"oxysterol binding protein like 6 [Source:HGNC Symbol;Acc:HGNC:16388]","synonyms":"ORP6","biotype":"protein_coding","ncbi_id":"114880","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. Transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":178194481,"end":178402891,"strand":1,"description":"oxysterol binding protein like 6 [Source:HGNC Symbol;Acc:HGNC:16388]"}, {"versioned_ensembl_gene_id":"ENSG00000260167.1","gene_symbol":"AC093249.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30585907,"end":30608593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260678.1","gene_symbol":"AC093249.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":30615256,"end":30615679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271070.1","gene_symbol":"GMCL1P2","gene_name":"germ cell-less, spermatogenesis associated 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420975","summary":null,"start":108367116,"end":108367938,"strand":1,"description":"germ cell-less, spermatogenesis associated 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42863]"}, {"versioned_ensembl_gene_id":"ENSG00000204531.17","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"MGC22487,Oct4,OCT3,OTF3","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31164337,"end":31180731,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000237095.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"KIAA0170,Em:AB023051.5,NFBD1","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30778290,"end":30796371,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000261588.1","gene_symbol":"AC093249.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30587662,"end":30587920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163686.14","gene_symbol":"ABHD6","gene_name":"abhydrolase domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57406","summary":null,"start":58237506,"end":58295693,"strand":1,"description":"abhydrolase domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21398]"}, {"versioned_ensembl_gene_id":"ENSG00000138439.11","gene_symbol":"FAM117B","gene_name":"family with sequence similarity 117 member B [Source:HGNC Symbol;Acc:HGNC:14440]","synonyms":"FLJ38771,ALS2CR13","biotype":"protein_coding","ncbi_id":"150864","summary":null,"start":202635188,"end":202769757,"strand":1,"description":"family with sequence similarity 117 member B [Source:HGNC Symbol;Acc:HGNC:14440]"}, {"versioned_ensembl_gene_id":"ENSG00000156853.12","gene_symbol":"ZNF689","gene_name":"zinc finger protein 689 [Source:HGNC Symbol;Acc:HGNC:25173]","synonyms":"FLJ90415","biotype":"protein_coding","ncbi_id":"115509","summary":null,"start":30602558,"end":30624012,"strand":-1,"description":"zinc finger protein 689 [Source:HGNC Symbol;Acc:HGNC:25173]"}, {"versioned_ensembl_gene_id":"ENSG00000080189.14","gene_symbol":"SLC35C2","gene_name":"solute carrier family 35 member C2 [Source:HGNC Symbol;Acc:HGNC:17117]","synonyms":"C20orf5,bA394O2.1,OVCOV1,CGI-15","biotype":"protein_coding","ncbi_id":"51006","summary":"This gene encodes a member of the triose-phosphate transporter protein family. This gene is regulated by oxygen tension, is induced in hypoxic trophoblast cells, and is overexpressed in ovarian cancer. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Jul 2013]","start":46345980,"end":46364458,"strand":-1,"description":"solute carrier family 35 member C2 [Source:HGNC Symbol;Acc:HGNC:17117]"}, {"versioned_ensembl_gene_id":"ENSG00000280695.1","gene_symbol":"AC226131.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64143780,"end":64147290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064393.15","gene_symbol":"HIPK2","gene_name":"homeodomain interacting protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:14402]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28996","summary":"This gene encodes a conserved serine/threonine kinase that is a member of the homeodomain-interacting protein kinase family. The encoded protein interacts with homeodomain transcription factors and many other transcription factors such as p53, and can function as both a corepressor and a coactivator depending on the transcription factor and its subcellular localization. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":139561570,"end":139777778,"strand":-1,"description":"homeodomain interacting protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:14402]"}, {"versioned_ensembl_gene_id":"ENSG00000274213.1","gene_symbol":"AC015912.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56914186,"end":56914533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142186.16","gene_symbol":"SCYL1","gene_name":"SCY1 like pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:14372]","synonyms":"NTKL,NKTL,MGC78454,HT019,GKLP,TRAP,TEIF,TAPK,P105","biotype":"protein_coding","ncbi_id":"57410","summary":"This gene encodes a transcriptional regulator belonging to the SCY1-like family of kinase-like proteins. The protein has a divergent N-terminal kinase domain that is thought to be catalytically inactive, and can bind specific DNA sequences through its C-terminal domain. It activates transcription of the telomerase reverse transcriptase and DNA polymerase beta genes. The protein has been localized to the nucleus, and also to the cytoplasm and centrosomes during mitosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":65525077,"end":65538704,"strand":1,"description":"SCY1 like pseudokinase 1 [Source:HGNC Symbol;Acc:HGNC:14372]"}, {"versioned_ensembl_gene_id":"ENSG00000255258.2","gene_symbol":"AP001979.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133783671,"end":133810376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260445.1","gene_symbol":"AC011904.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99869841,"end":99869894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262623.1","gene_symbol":"AC004584.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56951664,"end":56952404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260524.1","gene_symbol":"CYP3A52P","gene_name":"cytochrome P450 family 3 subfamily A member 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:42412]","synonyms":"CYP3A43-de4c6c","biotype":"unprocessed_pseudogene","ncbi_id":"106478983","summary":null,"start":99872168,"end":99872258,"strand":1,"description":"cytochrome P450 family 3 subfamily A member 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:42412]"}, {"versioned_ensembl_gene_id":"ENSG00000174652.17","gene_symbol":"ZNF266","gene_name":"zinc finger protein 266 [Source:HGNC Symbol;Acc:HGNC:13059]","synonyms":"HZF1","biotype":"protein_coding","ncbi_id":"10781","summary":"This gene encodes a protein containing many tandem zinc-finger motifs. Zinc fingers are protein or nucleic acid-binding domains, and may be involved in a variety of functions, including regulation of transcription. This gene is located in a cluster of similar genes encoding zinc finger proteins on chromosome 19. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012]","start":9412598,"end":9435578,"strand":-1,"description":"zinc finger protein 266 [Source:HGNC Symbol;Acc:HGNC:13059]"}, {"versioned_ensembl_gene_id":"ENSG00000121058.4","gene_symbol":"COIL","gene_name":"coilin [Source:HGNC Symbol;Acc:HGNC:2184]","synonyms":"p80-coilin,CLN80","biotype":"protein_coding","ncbi_id":"8161","summary":"The protein encoded by this gene is an integral component of Cajal bodies (also called coiled bodies). Cajal bodies are nuclear suborganelles of varying number and composition that are involved in the post-transcriptional modification of small nuclear and small nucleolar RNAs. The N-terminus of the coilin protein directs its self-oligomerization while the C-terminus influences the number of nuclear bodies assembled per cell. Differential methylation and phosphorylation of coilin likely influences its localization among nuclear bodies and the composition and assembly of Cajal bodies. This gene has pseudogenes on chromosome 4 and chromosome 14. [provided by RefSeq, Jul 2008]","start":56938187,"end":56961054,"strand":-1,"description":"coilin [Source:HGNC Symbol;Acc:HGNC:2184]"}, {"versioned_ensembl_gene_id":"ENSG00000239791.1","gene_symbol":"AC002310.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30572250,"end":30583860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251526.1","gene_symbol":"LINC02435","gene_name":"long intergenic non-protein coding RNA 2435 [Source:HGNC Symbol;Acc:HGNC:53366]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986311","summary":null,"start":123505279,"end":123527525,"strand":1,"description":"long intergenic non-protein coding RNA 2435 [Source:HGNC Symbol;Acc:HGNC:53366]"}, {"versioned_ensembl_gene_id":"ENSG00000249125.1","gene_symbol":"AC093821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123490268,"end":123522106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086288.11","gene_symbol":"NME8","gene_name":"NME/NM23 family member 8 [Source:HGNC Symbol;Acc:HGNC:16473]","synonyms":"TXNDC3,SPTRX2,NM23-H8,CILD6","biotype":"protein_coding","ncbi_id":"51314","summary":"This gene encodes a protein with an N-terminal thioredoxin domain and three C-terminal nucleoside diphosphate kinase (NDK) domains, but the NDK domains are thought to be catalytically inactive. The sea urchin ortholog of this gene encodes a component of sperm outer dynein arms, and the protein is implicated in ciliary function. Mutations in this gene are implicated in primary ciliary dyskinesia type 6.[provided by RefSeq, Nov 2009]","start":37848597,"end":37900401,"strand":1,"description":"NME/NM23 family member 8 [Source:HGNC Symbol;Acc:HGNC:16473]"}, {"versioned_ensembl_gene_id":"ENSG00000253259.1","gene_symbol":"AC103726.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":130892070,"end":130892785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262298.1","gene_symbol":"AC004584.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56939932,"end":56941275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165757.8","gene_symbol":"JCAD","gene_name":"junctional cadherin 5 associated [Source:HGNC Symbol;Acc:HGNC:29283]","synonyms":"KIAA1462","biotype":"protein_coding","ncbi_id":"57608","summary":"This gene encodes an endothelial cell-to-cell junction protein. Naturally occurring mutations in this gene are associated with coronary artery disease, late onset alzheimer disease, and emphysema distribution. [provided by RefSeq, Mar 2017]","start":30012800,"end":30115494,"strand":-1,"description":"junctional cadherin 5 associated [Source:HGNC Symbol;Acc:HGNC:29283]"}, {"versioned_ensembl_gene_id":"ENSG00000244623.1","gene_symbol":"OR2AE1","gene_name":"olfactory receptor family 2 subfamily AE member 1 [Source:HGNC Symbol;Acc:HGNC:15087]","synonyms":"OR2AE2","biotype":"protein_coding","ncbi_id":"81392","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":99875987,"end":99877057,"strand":-1,"description":"olfactory receptor family 2 subfamily AE member 1 [Source:HGNC Symbol;Acc:HGNC:15087]"}, {"versioned_ensembl_gene_id":"ENSG00000249464.5","gene_symbol":"LINC01091","gene_name":"long intergenic non-protein coding RNA 1091 [Source:HGNC Symbol;Acc:HGNC:27721]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285419","summary":null,"start":123650267,"end":123930406,"strand":1,"description":"long intergenic non-protein coding RNA 1091 [Source:HGNC Symbol;Acc:HGNC:27721]"}, {"versioned_ensembl_gene_id":"ENSG00000251235.3","gene_symbol":"SNRPCP2","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129566","summary":null,"start":76376675,"end":76377149,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49817]"}, {"versioned_ensembl_gene_id":"ENSG00000253992.1","gene_symbol":"AC103726.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130935409,"end":130949665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146833.15","gene_symbol":"TRIM4","gene_name":"tripartite motif containing 4 [Source:HGNC Symbol;Acc:HGNC:16275]","synonyms":"RNF87","biotype":"protein_coding","ncbi_id":"89122","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Its function has not been identified. Alternatively spliced transcript variants that encode different isoforms have been described.[provided by RefSeq, Jul 2010]","start":99876958,"end":99919600,"strand":-1,"description":"tripartite motif containing 4 [Source:HGNC Symbol;Acc:HGNC:16275]"}, {"versioned_ensembl_gene_id":"ENSG00000260418.1","gene_symbol":"AL023284.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136335714,"end":136336087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179869.14","gene_symbol":"ABCA13","gene_name":"ATP binding cassette subfamily A member 13 [Source:HGNC Symbol;Acc:HGNC:14638]","synonyms":"FLJ33951,FLJ33876","biotype":"protein_coding","ncbi_id":"154664","summary":"In human, the ATP-binding cassette (ABC) family of transmembrane transporters has at least 48 genes and 7 gene subfamilies. This gene is a member of ABC gene subfamily A (ABCA). Genes within the ABCA family typically encode several thousand amino acids. Like other ABC transmembrane transporter proteins, this protein has 12 or more transmembrane alpha-helix domains that likely arrange to form a single central chamber with multiple substrate binding sites. It is also predicted to have two large extracellular domains and two nucleotide binding domains as is typical for ABCA proteins. Alternative splice variants have been described but their biological validity has not been demonstrated.[provided by RefSeq, Mar 2009]","start":48171458,"end":48647496,"strand":1,"description":"ATP binding cassette subfamily A member 13 [Source:HGNC Symbol;Acc:HGNC:14638]"}, {"versioned_ensembl_gene_id":"ENSG00000250458.2","gene_symbol":"AC093767.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123861860,"end":123862015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258618.2","gene_symbol":"RPL21P9","gene_name":"ribosomal protein L21 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:19780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283562","summary":null,"start":67714545,"end":67715204,"strand":1,"description":"ribosomal protein L21 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:19780]"}, {"versioned_ensembl_gene_id":"ENSG00000155897.9","gene_symbol":"ADCY8","gene_name":"adenylate cyclase 8 [Source:HGNC Symbol;Acc:HGNC:239]","synonyms":"HBAC1,ADCY3,AC8","biotype":"protein_coding","ncbi_id":"114","summary":"Adenylate cyclase is a membrane bound enzyme that catalyses the formation of cyclic AMP from ATP. The enzymatic activity is under the control of several hormones, and different polypeptides participate in the transduction of the signal from the receptor to the catalytic moiety. Stimulatory or inhibitory receptors (Rs and Ri) interact with G proteins (Gs and Gi) that exhibit GTPase activity and they modulate the activity of the catalytic subunit of the adenylyl cyclase [provided by RefSeq, Jul 2008]","start":130780301,"end":131042426,"strand":-1,"description":"adenylate cyclase 8 [Source:HGNC Symbol;Acc:HGNC:239]"}, {"versioned_ensembl_gene_id":"ENSG00000134996.11","gene_symbol":"OSTF1","gene_name":"osteoclast stimulating factor 1 [Source:HGNC Symbol;Acc:HGNC:8510]","synonyms":"SH3P2,OSF,bA235O14.1","biotype":"protein_coding","ncbi_id":"26578","summary":"Osteoclast-stimulating factor-1 is an intracellular protein produced by osteoclasts that indirectly induces osteoclast formation and bone resorption (Reddy et al., 1998 [PubMed 10092216]).[supplied by OMIM, Mar 2008]","start":75088543,"end":75147265,"strand":1,"description":"osteoclast stimulating factor 1 [Source:HGNC Symbol;Acc:HGNC:8510]"}, {"versioned_ensembl_gene_id":"ENSG00000259935.1","gene_symbol":"AC009754.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52648634,"end":52649866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228489.1","gene_symbol":"RPL21P50","gene_name":"ribosomal protein L21 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36433]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271167","summary":null,"start":123745750,"end":123746226,"strand":-1,"description":"ribosomal protein L21 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:36433]"}, {"versioned_ensembl_gene_id":"ENSG00000260618.1","gene_symbol":"AC025917.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52577842,"end":52598709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271697.1","gene_symbol":"AL049779.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67735195,"end":67735350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226655.1","gene_symbol":"AC096732.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123744923,"end":123745673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139988.9","gene_symbol":"RDH12","gene_name":"retinol dehydrogenase 12 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:19977]","synonyms":"SDR7C2,RP53,LCA13,FLJ30273","biotype":"protein_coding","ncbi_id":"145226","summary":"The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]","start":67701886,"end":67734452,"strand":1,"description":"retinol dehydrogenase 12 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:HGNC:19977]"}, {"versioned_ensembl_gene_id":"ENSG00000233883.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30781550,"end":30791666,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000156795.6","gene_symbol":"WDYHV1","gene_name":"WDYHV motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25490]","synonyms":"FLJ10204,C8orf32","biotype":"protein_coding","ncbi_id":"55093","summary":null,"start":123416725,"end":123467230,"strand":1,"description":"WDYHV motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25490]"}, {"versioned_ensembl_gene_id":"ENSG00000283063.1","gene_symbol":"AC245088.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142349152,"end":142349664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255085.8","gene_symbol":"AF186192.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144700353,"end":144708517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261737.1","gene_symbol":"AL049597.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86703502,"end":86704462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282939.1","gene_symbol":"AC245088.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142352819,"end":142353358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243889.1","gene_symbol":"TRBV8-1","gene_name":"T-cell receptor beta variable 8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12244]","synonyms":"TRBV81,TCRBV8S1P,TCRBV30S1P","biotype":"TR_V_pseudogene","ncbi_id":"28588","summary":null,"start":142358639,"end":142358917,"strand":1,"description":"T-cell receptor beta variable 8-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12244]"}, {"versioned_ensembl_gene_id":"ENSG00000228122.1","gene_symbol":"MTND1P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42095]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873342","summary":null,"start":16876218,"end":16876421,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42095]"}, {"versioned_ensembl_gene_id":"ENSG00000231015.1","gene_symbol":"AL049594.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24679547,"end":24680991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237358.1","gene_symbol":"AC007064.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16876552,"end":16876902,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242771.1","gene_symbol":"TRBV5-2","gene_name":"T-cell receptor beta variable 5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12219]","synonyms":"TRBV52,TCRBV5S2P,TCRBV31S1","biotype":"TR_V_pseudogene","ncbi_id":"28613","summary":null,"start":142372640,"end":142372912,"strand":1,"description":"T-cell receptor beta variable 5-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12219]"}, {"versioned_ensembl_gene_id":"ENSG00000253648.1","gene_symbol":"AC018437.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15973315,"end":16000324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275607.1","gene_symbol":"AC135507.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58379217,"end":58379525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258759.1","gene_symbol":"AL049779.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67799004,"end":67799609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261584.1","gene_symbol":"AL513548.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26686241,"end":26687964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280906.1","gene_symbol":"AC225099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":243855738,"end":243856491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107951.14","gene_symbol":"MTPAP","gene_name":"mitochondrial poly(A) polymerase [Source:HGNC Symbol;Acc:HGNC:25532]","synonyms":"PAPD1,mtPAP,FLJ10486,SPAX4","biotype":"protein_coding","ncbi_id":"55149","summary":"The protein encoded by this gene is a member of the DNA polymerase type-B-like family. This enzyme synthesizes the 3' poly(A) tail of mitochondrial transcripts and plays a role in replication-dependent histone mRNA degradation.[provided by RefSeq, Jan 2011]","start":30309801,"end":30374448,"strand":-1,"description":"mitochondrial poly(A) polymerase [Source:HGNC Symbol;Acc:HGNC:25532]"}, {"versioned_ensembl_gene_id":"ENSG00000229930.1","gene_symbol":"AC138393.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":224030704,"end":224035056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274173.1","gene_symbol":"AL035661.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24931840,"end":24932983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225480.1","gene_symbol":"AC006548.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16897445,"end":16897546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211713.3","gene_symbol":"TRBV6-4","gene_name":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]","synonyms":"TCRBV6S4,TCRBV13S5,TRBV64","biotype":"TR_V_gene","ncbi_id":"28603","summary":null,"start":142380806,"end":142381261,"strand":1,"description":"T-cell receptor beta variable 6-4 [Source:HGNC Symbol;Acc:HGNC:12229]"}, {"versioned_ensembl_gene_id":"ENSG00000230481.2","gene_symbol":"IGKV1OR22-5","gene_name":"immunoglobulin kappa variable 1/OR22-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5773]","synonyms":"IGKVP7,IGKV1OR22-5A,IGKV1/OR22-5A,IGKV1/OR22-5","biotype":"IG_V_pseudogene","ncbi_id":"28850","summary":null,"start":16904219,"end":16904696,"strand":-1,"description":"immunoglobulin kappa variable 1/OR22-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5773]"}, {"versioned_ensembl_gene_id":"ENSG00000267182.1","gene_symbol":"SNRPCP20","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49835]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480292","summary":null,"start":5289200,"end":5289409,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49835]"}, {"versioned_ensembl_gene_id":"ENSG00000262621.4","gene_symbol":"AC025283.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3365099,"end":3479550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146066.2","gene_symbol":"HIGD2A","gene_name":"HIG1 hypoxia inducible domain family member 2A [Source:HGNC Symbol;Acc:HGNC:28311]","synonyms":"RCF1B,MGC2198","biotype":"protein_coding","ncbi_id":"192286","summary":"The protein encoded by this gene is a subunit of the cytochrome c oxidase complex (complex IV), which is the terminal enzyme in the mitochondrial respiratory chain. The encoded protein is an inner mitochondrial membrane protein and is a functional ortholog of the yeast respiratory supercomplex factor 1 (Rcf1). In mouse, the orthologous protein enhances cell survival under conditions of hypoxia. [provided by RefSeq, Sep 2016]","start":176388747,"end":176389771,"strand":1,"description":"HIG1 hypoxia inducible domain family member 2A [Source:HGNC Symbol;Acc:HGNC:28311]"}, {"versioned_ensembl_gene_id":"ENSG00000228134.1","gene_symbol":"UBE2V1P14","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52412]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289623","summary":null,"start":142543418,"end":142543975,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:52412]"}, {"versioned_ensembl_gene_id":"ENSG00000168297.15","gene_symbol":"PXK","gene_name":"PX domain containing serine/threonine kinase like [Source:HGNC Symbol;Acc:HGNC:23326]","synonyms":"Slob,FLJ20335","biotype":"protein_coding","ncbi_id":"54899","summary":"This gene encodes a phox (PX) domain-containing protein which may be involved in synaptic transmission and the ligand-induced internalization and degradation of epidermal growth factors. Variations in this gene may be associated with susceptibility to systemic lupus erythematosus (SLE). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":58332880,"end":58426126,"strand":1,"description":"PX domain containing serine/threonine kinase like [Source:HGNC Symbol;Acc:HGNC:23326]"}, {"versioned_ensembl_gene_id":"ENSG00000229781.1","gene_symbol":"AC013444.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142854095,"end":142855998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211714.3","gene_symbol":"TRBV7-3","gene_name":"T-cell receptor beta variable 7-3 [Source:HGNC Symbol;Acc:HGNC:12237]","synonyms":"TRBV73,TCRBV7S3,TCRBV6S1A1N1","biotype":"TR_V_gene","ncbi_id":"28595","summary":null,"start":142384329,"end":142384841,"strand":1,"description":"T-cell receptor beta variable 7-3 [Source:HGNC Symbol;Acc:HGNC:12237]"}, {"versioned_ensembl_gene_id":"ENSG00000206314.9","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"G18.1a,G18.2,AGS4,G18,G18.1b,NG1,C6orf9","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32148372,"end":32153129,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000235707.2","gene_symbol":"AL158073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75401889,"end":75402992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000048162.20","gene_symbol":"NOP16","gene_name":"NOP16 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:26934]","synonyms":"LOC51491,HSPC185,HSPC111","biotype":"protein_coding","ncbi_id":"51491","summary":"This gene encodes a protein that is localized to the nucleolus. Expression of this gene is induced by estrogens and Myc protein and is a marker of poor patient survival in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":176383938,"end":176388975,"strand":-1,"description":"NOP16 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:26934]"}, {"versioned_ensembl_gene_id":"ENSG00000180229.12","gene_symbol":"HERC2P3","gene_name":"hect domain and RLD 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4871]","synonyms":"D15F37S4,LOC283755","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"283755","summary":null,"start":20379495,"end":20506180,"strand":-1,"description":"hect domain and RLD 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4871]"}, {"versioned_ensembl_gene_id":"ENSG00000183066.14","gene_symbol":"WBP2NL","gene_name":"WBP2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:28389]","synonyms":"PAWP,MGC26816,GRAMD7,FLJ26145","biotype":"protein_coding","ncbi_id":"164684","summary":"WBP2NL is a sperm-specific WW domain-binding protein that promotes meiotic resumption and pronuclear development during oocyte fertilization (Wu et al., 2007 [PubMed 17289678]).[supplied by OMIM, Mar 2008]","start":41998725,"end":42058456,"strand":1,"description":"WBP2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:28389]"}, {"versioned_ensembl_gene_id":"ENSG00000231098.1","gene_symbol":"AC008154.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134284500,"end":134286055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250356.1","gene_symbol":"HSPE1P23","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:49342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481676","summary":null,"start":74917822,"end":74918138,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:49342]"}, {"versioned_ensembl_gene_id":"ENSG00000097033.14","gene_symbol":"SH3GLB1","gene_name":"SH3 domain containing GRB2 like, endophilin B1 [Source:HGNC Symbol;Acc:HGNC:10833]","synonyms":"PPP1R70,KIAA0491,CGI-61,Bif-1","biotype":"protein_coding","ncbi_id":"51100","summary":"This gene encodes a SRC homology 3 domain-containing protein. The encoded protein interacts with the proapoptotic member of the Bcl-2 family, Bcl-2-associated X protein (Bax) and may be involved in regulating apoptotic signaling pathways. This protein may also be involved in maintaining mitochondrial morphology. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":86704570,"end":86748184,"strand":1,"description":"SH3 domain containing GRB2 like, endophilin B1 [Source:HGNC Symbol;Acc:HGNC:10833]"}, {"versioned_ensembl_gene_id":"ENSG00000086289.11","gene_symbol":"EPDR1","gene_name":"ependymin related 1 [Source:HGNC Symbol;Acc:HGNC:17572]","synonyms":"UCC1,MERP1,MERP-1,EPDR","biotype":"protein_coding","ncbi_id":"54749","summary":"The protein encoded by this gene is a type II transmembrane protein that is similar to two families of cell adhesion molecules, the protocadherins and ependymins. This protein may play a role in calcium-dependent cell adhesion. This protein is glycosylated, and the orthologous mouse protein is localized to the lysosome. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, Aug 2011]","start":37683843,"end":37951941,"strand":1,"description":"ependymin related 1 [Source:HGNC Symbol;Acc:HGNC:17572]"}, {"versioned_ensembl_gene_id":"ENSG00000269191.1","gene_symbol":"AC005387.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18532908,"end":18536188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161798.6","gene_symbol":"AQP5","gene_name":"aquaporin 5 [Source:HGNC Symbol;Acc:HGNC:638]","synonyms":null,"biotype":"protein_coding","ncbi_id":"362","summary":"Aquaporin 5 (AQP5) is a water channel protein. Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein (MIP or AQP0). Aquaporin 5 plays a role in the generation of saliva, tears and pulmonary secretions. AQP0, AQP2, AQP5, and AQP6 are closely related and all map to 12q13. [provided by RefSeq, Jul 2008]","start":49961870,"end":49965681,"strand":1,"description":"aquaporin 5 [Source:HGNC Symbol;Acc:HGNC:638]"}, {"versioned_ensembl_gene_id":"ENSG00000268938.2","gene_symbol":"AC005387.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18531613,"end":18532632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223461.1","gene_symbol":"AC004471.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19121529,"end":19124503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272682.1","gene_symbol":"AC004471.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19124309,"end":19128449,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270945.1","gene_symbol":"HSPE1P7","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49327]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132346","summary":null,"start":74612596,"end":74613221,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49327]"}, {"versioned_ensembl_gene_id":"ENSG00000249717.1","gene_symbol":"AC110760.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74955974,"end":74970362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143756.11","gene_symbol":"FBXO28","gene_name":"F-box protein 28 [Source:HGNC Symbol;Acc:HGNC:29046]","synonyms":"FLJ10766,Fbx28,CENP-30,KIAA0483","biotype":"protein_coding","ncbi_id":"23219","summary":"Members of the F-box protein family, such as FBXO28, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":224114087,"end":224162047,"strand":1,"description":"F-box protein 28 [Source:HGNC Symbol;Acc:HGNC:29046]"}, {"versioned_ensembl_gene_id":"ENSG00000169116.11","gene_symbol":"PARM1","gene_name":"prostate androgen-regulated mucin-like protein 1 [Source:HGNC Symbol;Acc:HGNC:24536]","synonyms":"WSC4,DKFZP564O0823,Cipar1","biotype":"protein_coding","ncbi_id":"25849","summary":null,"start":74933095,"end":75050115,"strand":1,"description":"prostate androgen-regulated mucin-like protein 1 [Source:HGNC Symbol;Acc:HGNC:24536]"}, {"versioned_ensembl_gene_id":"ENSG00000282512.1","gene_symbol":"AC131056.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36249651,"end":36250970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168411.13","gene_symbol":"RFWD3","gene_name":"ring finger and WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:25539]","synonyms":"RNF201,FLJ10520","biotype":"protein_coding","ncbi_id":"55159","summary":null,"start":74621394,"end":74666881,"strand":-1,"description":"ring finger and WD repeat domain 3 [Source:HGNC Symbol;Acc:HGNC:25539]"}, {"versioned_ensembl_gene_id":"ENSG00000269699.5","gene_symbol":"ZIM2","gene_name":"zinc finger imprinted 2 [Source:HGNC Symbol;Acc:HGNC:12875]","synonyms":"ZNF656","biotype":"protein_coding","ncbi_id":"23619","summary":"In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5' exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. This is in contrast to mouse and cow, where ZIM2 and PEG3 genes do not share exons in common, and the imprinting status of ZIM2 is also not conserved amongst mammals. Additional 5' alternatively spliced transcripts encoding the same protein have been found for the human ZIM2 gene. [provided by RefSeq, Oct 2010]","start":56774552,"end":56840729,"strand":-1,"description":"zinc finger imprinted 2 [Source:HGNC Symbol;Acc:HGNC:12875]"}, {"versioned_ensembl_gene_id":"ENSG00000176273.14","gene_symbol":"SLC35G1","gene_name":"solute carrier family 35 member G1 [Source:HGNC Symbol;Acc:HGNC:26607]","synonyms":"TMEM20,FLJ33990,C10orf60","biotype":"protein_coding","ncbi_id":"159371","summary":"This gene encodes a transmembrane protein which is a member of the drug/metabolite transporter protein superfamily. The encoded protein may play a role in the regulation of calcium levels inside the cell. [provided by RefSeq, Sep 2016]","start":93893973,"end":93956062,"strand":1,"description":"solute carrier family 35 member G1 [Source:HGNC Symbol;Acc:HGNC:26607]"}, {"versioned_ensembl_gene_id":"ENSG00000257378.1","gene_symbol":"AC025154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49954639,"end":49956125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257588.1","gene_symbol":"AC025154.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49951512,"end":49962924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112782.15","gene_symbol":"CLIC5","gene_name":"chloride intracellular channel 5 [Source:HGNC Symbol;Acc:HGNC:13517]","synonyms":"DFNB102","biotype":"protein_coding","ncbi_id":"53405","summary":"This gene encodes a member of the chloride intracellular channel (CLIC) family of chloride ion channels. The encoded protein associates with actin-based cytoskeletal structures and may play a role in multiple processes including hair cell stereocilia formation, myoblast proliferation and glomerular podocyte and endothelial cell maintenance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":45898451,"end":46080395,"strand":-1,"description":"chloride intracellular channel 5 [Source:HGNC Symbol;Acc:HGNC:13517]"}, {"versioned_ensembl_gene_id":"ENSG00000248165.1","gene_symbol":"AC110760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74993877,"end":75034824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132164.9","gene_symbol":"SLC6A11","gene_name":"solute carrier family 6 member 11 [Source:HGNC Symbol;Acc:HGNC:11044]","synonyms":"GAT3","biotype":"protein_coding","ncbi_id":"6538","summary":"The protein encoded by this gene is a sodium-dependent transporter that uptakes gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, which ends the GABA neurotransmission. Defects in this gene may result in epilepsy, behavioral problems, or intellectual problems. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":10816200,"end":10940733,"strand":1,"description":"solute carrier family 6 member 11 [Source:HGNC Symbol;Acc:HGNC:11044]"}, {"versioned_ensembl_gene_id":"ENSG00000167580.7","gene_symbol":"AQP2","gene_name":"aquaporin 2 [Source:HGNC Symbol;Acc:HGNC:634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"359","summary":"This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family, some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant and recessive forms of nephrogenic diabetes insipidus. [provided by RefSeq, Oct 2008]","start":49950741,"end":49958881,"strand":1,"description":"aquaporin 2 [Source:HGNC Symbol;Acc:HGNC:634]"}, {"versioned_ensembl_gene_id":"ENSG00000106483.11","gene_symbol":"SFRP4","gene_name":"secreted frizzled related protein 4 [Source:HGNC Symbol;Acc:HGNC:10778]","synonyms":"frpHE,FRP-4","biotype":"protein_coding","ncbi_id":"6424","summary":"Secreted frizzled-related protein 4 (SFRP4) is a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins. SFRPs act as soluble modulators of Wnt signaling. The expression of SFRP4 in ventricular myocardium correlates with apoptosis related gene expression. [provided by RefSeq, Jul 2008]","start":37905932,"end":38025695,"strand":-1,"description":"secreted frizzled related protein 4 [Source:HGNC Symbol;Acc:HGNC:10778]"}, {"versioned_ensembl_gene_id":"ENSG00000206312.7","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32152449,"end":32181676,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000250833.1","gene_symbol":"DNM1P17","gene_name":"dynamin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:21134]","synonyms":"DNM1DN17@,DNM1DN17","biotype":"unprocessed_pseudogene","ncbi_id":"100131084","summary":null,"start":30353706,"end":30357365,"strand":1,"description":"dynamin 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:21134]"}, {"versioned_ensembl_gene_id":"ENSG00000241621.1","gene_symbol":"GOLGA2P6","gene_name":"golgin A2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44948]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729668","summary":null,"start":30364410,"end":30374386,"strand":-1,"description":"golgin A2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44948]"}, {"versioned_ensembl_gene_id":"ENSG00000232633.4","gene_symbol":"AC079465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113323028,"end":113437174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096092.5","gene_symbol":"TMEM14A","gene_name":"transmembrane protein 14A [Source:HGNC Symbol;Acc:HGNC:21076]","synonyms":"PTD011,C6orf73","biotype":"protein_coding","ncbi_id":"28978","summary":null,"start":52671109,"end":52686588,"strand":1,"description":"transmembrane protein 14A [Source:HGNC Symbol;Acc:HGNC:21076]"}, {"versioned_ensembl_gene_id":"ENSG00000134815.18","gene_symbol":"DHX34","gene_name":"DExH-box helicase 34 [Source:HGNC Symbol;Acc:HGNC:16719]","synonyms":"KIAA0134,DDX34","biotype":"protein_coding","ncbi_id":"9704","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. It is mapped to the glioma 19q tumor suppressor region and is a tumor suppressor candidate gene. [provided by RefSeq, Jul 2008]","start":47349281,"end":47382704,"strand":1,"description":"DExH-box helicase 34 [Source:HGNC Symbol;Acc:HGNC:16719]"}, {"versioned_ensembl_gene_id":"ENSG00000230516.1","gene_symbol":"AL589642.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32643103,"end":32645026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212122.3","gene_symbol":"TSSK1B","gene_name":"testis specific serine kinase 1B [Source:HGNC Symbol;Acc:HGNC:14968]","synonyms":"TSSK1,STK22D,SPOGA4,FKSG81","biotype":"protein_coding","ncbi_id":"83942","summary":"TSSK1 belongs to a family of serine/threonine kinases highly expressed in testis (Hao et al., 2004 [PubMed 15044604]).[supplied by OMIM, Mar 2008]","start":113432554,"end":113435031,"strand":-1,"description":"testis specific serine kinase 1B [Source:HGNC Symbol;Acc:HGNC:14968]"}, {"versioned_ensembl_gene_id":"ENSG00000236773.1","gene_symbol":"AC092809.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224175476,"end":224175706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223440.1","gene_symbol":"AL589642.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32633454,"end":32648685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228904.3","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"D84394.7,USP8P,KIAA0055-hom","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31265372,"end":31268544,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000216613.2","gene_symbol":"AL023284.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136419847,"end":136420425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261273.1","gene_symbol":"AC138512.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88234785,"end":88302511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122728.6","gene_symbol":"TAF1L","gene_name":"TATA-box binding protein associated factor 1 like [Source:HGNC Symbol;Acc:HGNC:18056]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138474","summary":"This locus is intronless, and apparently arose in the primate lineage from retrotransposition of the transcript from the multi-exon TAF1 locus on the X chromosome. The gene is expressed in male germ cells, and the product has been shown to function interchangeably with the TAF1 product. [provided by RefSeq, Aug 2015]","start":32629454,"end":32635669,"strand":-1,"description":"TATA-box binding protein associated factor 1 like [Source:HGNC Symbol;Acc:HGNC:18056]"}, {"versioned_ensembl_gene_id":"ENSG00000224510.2","gene_symbol":"POLR2KP2","gene_name":"RNA polymerase II subunit K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42652]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129174","summary":null,"start":48134358,"end":48134534,"strand":-1,"description":"RNA polymerase II subunit K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42652]"}, {"versioned_ensembl_gene_id":"ENSG00000225954.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31277583,"end":31279034,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000172795.15","gene_symbol":"DCP2","gene_name":"decapping mRNA 2 [Source:HGNC Symbol;Acc:HGNC:24452]","synonyms":"NUDT20","biotype":"protein_coding","ncbi_id":"167227","summary":"The protein encoded by this gene is a key component of an mRNA-decapping complex required for degradation of mRNAs, both in normal mRNA turnover, and in nonsense-mediated mRNA decay (NMD). It removes the 7-methyl guanine cap structure from mRNA, prior to its degradation from the 5' end. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jun 2011]","start":112976702,"end":113020970,"strand":1,"description":"decapping mRNA 2 [Source:HGNC Symbol;Acc:HGNC:24452]"}, {"versioned_ensembl_gene_id":"ENSG00000238001.2","gene_symbol":"SNRPCP1","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49816]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288596","summary":null,"start":32676063,"end":32676520,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49816]"}, {"versioned_ensembl_gene_id":"ENSG00000206450.11","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31259328,"end":31347305,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000143753.12","gene_symbol":"DEGS1","gene_name":"delta 4-desaturase, sphingolipid 1 [Source:HGNC Symbol;Acc:HGNC:13709]","synonyms":"FADS7,DES1,Des-1,DEGS-1,MLD","biotype":"protein_coding","ncbi_id":"8560","summary":"This gene encodes a member of the membrane fatty acid desaturase family which is responsible for inserting double bonds into specific positions in fatty acids. This protein contains three His-containing consensus motifs that are characteristic of a group of membrane fatty acid desaturases. It is predicted to be a multiple membrane-spanning protein localized to the endoplasmic reticulum. Overexpression of this gene inhibited biosynthesis of the EGF receptor, suggesting a possible role of a fatty acid desaturase in regulating biosynthetic processing of the EGF receptor. [provided by RefSeq, Mar 2010]","start":224175756,"end":224193441,"strand":1,"description":"delta 4-desaturase, sphingolipid 1 [Source:HGNC Symbol;Acc:HGNC:13709]"}, {"versioned_ensembl_gene_id":"ENSG00000230867.1","gene_symbol":"AL157884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32727069,"end":32727522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187037.8","gene_symbol":"GPR141","gene_name":"G protein-coupled receptor 141 [Source:HGNC Symbol;Acc:HGNC:19997]","synonyms":"PGR13","biotype":"protein_coding","ncbi_id":"353345","summary":"GPR141 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003 [PubMed 14623098]).[supplied by OMIM, Mar 2008]","start":37683796,"end":37833788,"strand":1,"description":"G protein-coupled receptor 141 [Source:HGNC Symbol;Acc:HGNC:19997]"}, {"versioned_ensembl_gene_id":"ENSG00000180764.13","gene_symbol":"PIPSL","gene_name":"PIP5K1A and PSMD4-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:23733]","synonyms":"PSMD4P2,PIP5K1P3,PIP5K1L1,PIP5K1A-PSMD4","biotype":"transcribed_processed_pseudogene","ncbi_id":"266971","summary":"This locus is a transcribed pseudogene with similarity to two adjacent chromosome 1 loci: phosphatidylinositol-4-phosphate 5-kinase, type I, alpha (PIP5K1A, GeneID 8394) and proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 (PSMD4, GeneID 5710). The pseudogene is believed to have occurred from L1 retrotransposition into chromosome 10 of a read-through transcript between the two adjacent loci. Evidence of transcription has been found (PubMed IDs: 16344562 and 17623810), but the latter publication found no evidence that the predicted protein is translated. The NCBI RefSeq Project therefore continues to treat this as a transcribed pseudogene. [provided by RefSeq, Jan 2009]","start":93958191,"end":93961540,"strand":-1,"description":"PIP5K1A and PSMD4-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:23733]"}, {"versioned_ensembl_gene_id":"ENSG00000218424.2","gene_symbol":"NDUFS5P1","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44039]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996944","summary":null,"start":136475862,"end":136476150,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44039]"}, {"versioned_ensembl_gene_id":"ENSG00000228019.1","gene_symbol":"AC006480.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67307605,"end":67308356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106610.14","gene_symbol":"STAG3L4","gene_name":"stromal antigen 3-like 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33887]","synonyms":"FLJ13195,STAG3L4P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"64940","summary":null,"start":67302621,"end":67321526,"strand":1,"description":"stromal antigen 3-like 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33887]"}, {"versioned_ensembl_gene_id":"ENSG00000220660.2","gene_symbol":"AL023284.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":136364129,"end":136365079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189046.10","gene_symbol":"ALKBH2","gene_name":"alkB homolog 2, alpha-ketoglutarate dependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:32487]","synonyms":"MGC90512,ABH2","biotype":"protein_coding","ncbi_id":"121642","summary":"The Escherichia coli AlkB protein protects against the cytotoxicity of methylating agents by repair of the specific DNA lesions generated in single-stranded DNA. ALKBH2 and ALKBH3 (MIM 610603) are E. coli AlkB homologs that catalyze the removal of 1-methyladenine and 3-methylcytosine (Duncan et al., 2002 [PubMed 12486230]).[supplied by OMIM, Mar 2008]","start":109088188,"end":109093631,"strand":-1,"description":"alkB homolog 2, alpha-ketoglutarate dependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:32487]"}, {"versioned_ensembl_gene_id":"ENSG00000259963.1","gene_symbol":"AC007012.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6721786,"end":6721960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278171.1","gene_symbol":"AL137028.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64278306,"end":64278561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260817.2","gene_symbol":"AC074051.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5260686,"end":5261043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225314.1","gene_symbol":"AC018634.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37821210,"end":37821610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204542.2","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31111223,"end":31112559,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000204314.10","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32148359,"end":32154373,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000075290.7","gene_symbol":"WNT8B","gene_name":"Wnt family member 8B [Source:HGNC Symbol;Acc:HGNC:12789]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7479","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 95%, 86% and 71% amino acid identity to the mouse, zebrafish and Xenopus Wnt8B proteins, respectively. The expression patterns of the human and mouse genes appear identical and are restricted to the developing brain. The chromosomal location of this gene to 10q24 suggests it as a candidate gene for partial epilepsy. [provided by RefSeq, Jul 2008]","start":100463041,"end":100483744,"strand":1,"description":"Wnt family member 8B [Source:HGNC Symbol;Acc:HGNC:12789]"}, {"versioned_ensembl_gene_id":"ENSG00000160862.12","gene_symbol":"AZGP1","gene_name":"alpha-2-glycoprotein 1, zinc-binding [Source:HGNC Symbol;Acc:HGNC:910]","synonyms":"ZAG,ZA2G","biotype":"protein_coding","ncbi_id":"563","summary":null,"start":99966720,"end":99976157,"strand":-1,"description":"alpha-2-glycoprotein 1, zinc-binding [Source:HGNC Symbol;Acc:HGNC:910]"}, {"versioned_ensembl_gene_id":"ENSG00000058799.14","gene_symbol":"YIPF1","gene_name":"Yip1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:25231]","synonyms":"FinGER1,DJ167A19.1","biotype":"protein_coding","ncbi_id":"54432","summary":null,"start":53851719,"end":53889834,"strand":-1,"description":"Yip1 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:25231]"}, {"versioned_ensembl_gene_id":"ENSG00000277339.2","gene_symbol":"NPBWR2","gene_name":"neuropeptides B and W receptor 2 [Source:HGNC Symbol;Acc:HGNC:4530]","synonyms":"GPR8","biotype":"protein_coding","ncbi_id":"2832","summary":"The protein encoded by this gene is an integral membrane protein and G protein-coupled receptor. The encoded protein is similar in sequence to another G protein-coupled receptor (GPR7), and it is structurally similar to opioid and somatostatin receptors. This protein binds neuropeptides B and W. This gene is intronless and is expressed primarily in the frontal cortex of the brain. [provided by RefSeq, Jul 2008]","start":64105820,"end":64107171,"strand":-1,"description":"neuropeptides B and W receptor 2 [Source:HGNC Symbol;Acc:HGNC:4530]"}, {"versioned_ensembl_gene_id":"ENSG00000261816.1","gene_symbol":"AC134312.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88191486,"end":88193667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131845.14","gene_symbol":"ZNF304","gene_name":"zinc finger protein 304 [Source:HGNC Symbol;Acc:HGNC:13505]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57343","summary":"This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein functions as a transcriptional repressor that recruits a corepressor complex to stimulate promoter hypermethylation and transcriptional silencing of target genes. Expression of this gene is upregulated in colorectal, ovarian and breast cancer, and this gene may promote cancer cell survival, growth and invasion. [provided by RefSeq, Jul 2016]","start":57351307,"end":57359898,"strand":1,"description":"zinc finger protein 304 [Source:HGNC Symbol;Acc:HGNC:13505]"}, {"versioned_ensembl_gene_id":"ENSG00000235478.4","gene_symbol":"LINC01664","gene_name":"long intergenic non-protein coding RNA 1664 [Source:HGNC Symbol;Acc:HGNC:52452]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996342","summary":null,"start":17121586,"end":17132104,"strand":1,"description":"long intergenic non-protein coding RNA 1664 [Source:HGNC Symbol;Acc:HGNC:52452]"}, {"versioned_ensembl_gene_id":"ENSG00000235251.2","gene_symbol":"AC093155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87044935,"end":87045871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277571.2","gene_symbol":"ELANE","gene_name":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]","synonyms":"ELA2,NE,HNE,HLE","biotype":"protein_coding","ncbi_id":"1991","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode structurally similar proteins. The encoded preproprotein is proteolytically processed to generate the active protease. Following activation, this protease hydrolyzes proteins within specialized neutrophil lysosomes, called azurophil granules, as well as proteins of the extracellular matrix. The enzyme may play a role in degenerative and inflammatory diseases through proteolysis of collagen-IV and elastin. This protein also degrades the outer membrane protein A (OmpA) of E. coli as well as the virulence factors of such bacteria as Shigella, Salmonella and Yersinia. Mutations in this gene are associated with cyclic neutropenia and severe congenital neutropenia (SCN). This gene is present in a gene cluster on chromosome 19. [provided by RefSeq, Jan 2016]","start":851006,"end":856290,"strand":1,"description":"elastase, neutrophil expressed [Source:HGNC Symbol;Acc:HGNC:3309]"}, {"versioned_ensembl_gene_id":"ENSG00000225067.4","gene_symbol":"RPL23AP2","gene_name":"ribosomal protein L23a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10319]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401904","summary":null,"start":15611657,"end":15612122,"strand":1,"description":"ribosomal protein L23a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10319]"}, {"versioned_ensembl_gene_id":"ENSG00000261327.4","gene_symbol":"AC134312.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88177298,"end":88178941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256280.1","gene_symbol":"AP006289.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63834667,"end":63834943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258973.1","gene_symbol":"AL096870.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24332310,"end":24337382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100294.12","gene_symbol":"MCAT","gene_name":"malonyl-CoA-acyl carrier protein transacylase [Source:HGNC Symbol;Acc:HGNC:29622]","synonyms":"MT,MCT1,MCT,FASN2C,fabD,NET62","biotype":"protein_coding","ncbi_id":"27349","summary":"The protein encoded by this gene is found exclusively in the mitochondrion, where it catalyzes the transfer of a malonyl group from malonyl-CoA to the mitochondrial acyl carrier protein. The encoded protein may be part of a fatty acid synthase complex that is more like the type II prokaryotic and plastid complexes rather than the type I human cytosolic complex. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2012]","start":43132206,"end":43143394,"strand":-1,"description":"malonyl-CoA-acyl carrier protein transacylase [Source:HGNC Symbol;Acc:HGNC:29622]"}, {"versioned_ensembl_gene_id":"ENSG00000248484.1","gene_symbol":"AC113391.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176707356,"end":176726243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240707.2","gene_symbol":"LINC01168","gene_name":"long intergenic non-protein coding RNA 1168 [Source:HGNC Symbol;Acc:HGNC:49537]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399829","summary":null,"start":132965534,"end":132976354,"strand":1,"description":"long intergenic non-protein coding RNA 1168 [Source:HGNC Symbol;Acc:HGNC:49537]"}, {"versioned_ensembl_gene_id":"ENSG00000168405.16","gene_symbol":"CMAHP","gene_name":"cytidine monophospho-N-acetylneuraminic acid hydroxylase, pseudogene [Source:HGNC Symbol;Acc:HGNC:2098]","synonyms":"CMAH","biotype":"transcribed_unitary_pseudogene","ncbi_id":"8418","summary":"Sialic acids are terminal components of the carbohydrate chains of glycoconjugates involved in ligand-receptor, cell-cell, and cell-pathogen interactions. The two most common forms of sialic acid found in mammalian cells are N-acetylneuraminic acid (Neu5Ac) and its hydroxylated derivative, N-glycolylneuraminic acid (Neu5Gc). Studies of sialic acid distribution show that Neu5Gc is not detectable in normal human tissues although it was an abundant sialic acid in other mammals. Neu5Gc is, in actuality, immunogenic in humans. The absense of Neu5Gc in humans is due to a deletion within the human gene CMAH encoding cytidine monophosphate-N-acetylneuraminic acid hydroxylase, an enzyme responsible for Neu5Gc biosynthesis. Sequences encoding the mouse, pig, and chimpanzee hydroxylase enzymes were obtained by cDNA cloning and found to be highly homologous. However, the homologous human cDNA differs from these cDNAs by a 92-bp deletion in the 5' region. This deletion, corresponding to exon 6 of the mouse hydroxylase gene, causes a frameshift mutation and premature termination of the polypeptide chain in human. It seems unlikely that the truncated human hydroxylase mRNA encodes for an active enzyme explaining why Neu5Gc is undetectable in normal human tissues. Human genomic DNA also shows evidence of this deletion which does not occur in the genomes of African great apes. Nonetheless, the CMAH gene maps to 6p21.32 in humans and great apes indicating that mutation of the CMAH gene occurred following human divergence from chimpanzees and bonobos. [provided by RefSeq, Jul 2008]","start":25081068,"end":25166555,"strand":-1,"description":"cytidine monophospho-N-acetylneuraminic acid hydroxylase, pseudogene [Source:HGNC Symbol;Acc:HGNC:2098]"}, {"versioned_ensembl_gene_id":"ENSG00000176896.8","gene_symbol":"TCEANC","gene_name":"transcription elongation factor A N-terminal and central domain containing [Source:HGNC Symbol;Acc:HGNC:28277]","synonyms":"MGC17403","biotype":"protein_coding","ncbi_id":"170082","summary":null,"start":13653189,"end":13681964,"strand":1,"description":"transcription elongation factor A N-terminal and central domain containing [Source:HGNC Symbol;Acc:HGNC:28277]"}, {"versioned_ensembl_gene_id":"ENSG00000168005.8","gene_symbol":"C11orf84","gene_name":"chromosome 11 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:25115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"144097","summary":null,"start":63813388,"end":63827718,"strand":1,"description":"chromosome 11 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:25115]"}, {"versioned_ensembl_gene_id":"ENSG00000215477.2","gene_symbol":"RCN1P1","gene_name":"reticulocalbin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39205]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442234","summary":null,"start":87121693,"end":87122688,"strand":-1,"description":"reticulocalbin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39205]"}, {"versioned_ensembl_gene_id":"ENSG00000076108.11","gene_symbol":"BAZ2A","gene_name":"bromodomain adjacent to zinc finger domain 2A [Source:HGNC Symbol;Acc:HGNC:962]","synonyms":"WALp3,TIP5,KIAA0314","biotype":"protein_coding","ncbi_id":"11176","summary":null,"start":56595596,"end":56636816,"strand":-1,"description":"bromodomain adjacent to zinc finger domain 2A [Source:HGNC Symbol;Acc:HGNC:962]"}, {"versioned_ensembl_gene_id":"ENSG00000163357.10","gene_symbol":"DCST1","gene_name":"DC-STAMP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26539]","synonyms":"FLJ32785","biotype":"protein_coding","ncbi_id":"149095","summary":"This gene encodes a protein with a domain similar to one found in dendritic cells (PMID:11169400) which play a key role in antigen processing and display for immune responses. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":155033824,"end":155050930,"strand":1,"description":"DC-STAMP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26539]"}, {"versioned_ensembl_gene_id":"ENSG00000236507.1","gene_symbol":"BX470209.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89801727,"end":89803061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175592.8","gene_symbol":"FOSL1","gene_name":"FOS like 1, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:13718]","synonyms":"fra-1","biotype":"protein_coding","ncbi_id":"8061","summary":"The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":65892049,"end":65900573,"strand":-1,"description":"FOS like 1, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:13718]"}, {"versioned_ensembl_gene_id":"ENSG00000074317.10","gene_symbol":"SNCB","gene_name":"synuclein beta [Source:HGNC Symbol;Acc:HGNC:11140]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6620","summary":"This gene encodes a member of a small family of proteins that inhibit phospholipase D2 and may function in neuronal plasticity. The encoded protein is abundant in lesions of patients with Alzheimer disease. A mutation in this gene was found in individuals with dementia with Lewy bodies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":176620084,"end":176630556,"strand":-1,"description":"synuclein beta [Source:HGNC Symbol;Acc:HGNC:11140]"}, {"versioned_ensembl_gene_id":"ENSG00000021355.12","gene_symbol":"SERPINB1","gene_name":"serpin family B member 1 [Source:HGNC Symbol;Acc:HGNC:3311]","synonyms":"PI2,ELANH2,EI,anti-elastase","biotype":"protein_coding","ncbi_id":"1992","summary":"The protein encoded by this gene is a member of the serpin family of proteinase inhibitors. Members of this family maintain homeostasis by neutralizing overexpressed proteinase activity through their function as suicide substrates. This protein inhibits the neutrophil-derived proteinases neutrophil elastase, cathepsin G, and proteinase-3 and thus protects tissues from damage at inflammatory sites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":2832332,"end":2842006,"strand":-1,"description":"serpin family B member 1 [Source:HGNC Symbol;Acc:HGNC:3311]"}, {"versioned_ensembl_gene_id":"ENSG00000236746.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":30035070,"end":30037031,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000281020.2","gene_symbol":"SNTG2","gene_name":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]","synonyms":"SYN5,G2SYN","biotype":"protein_coding","ncbi_id":"54221","summary":"This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq, Jul 2008]","start":1316265,"end":1365970,"strand":1,"description":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]"}, {"versioned_ensembl_gene_id":"ENSG00000259837.1","gene_symbol":"LINC01904","gene_name":"long intergenic non-protein coding RNA 1904 [Source:HGNC Symbol;Acc:HGNC:52723]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388456","summary":null,"start":926083,"end":927993,"strand":-1,"description":"long intergenic non-protein coding RNA 1904 [Source:HGNC Symbol;Acc:HGNC:52723]"}, {"versioned_ensembl_gene_id":"ENSG00000281232.1","gene_symbol":"AC108489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1340838,"end":1344763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259697.1","gene_symbol":"AC126323.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62196145,"end":62203318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175061.17","gene_symbol":"LRRC75A-AS1","gene_name":"LRRC75A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28619]","synonyms":"FAM211A-AS1,C17orf76-AS1,C17orf45,NCRNA00188,MGC40157","biotype":"processed_transcript","ncbi_id":"125144","summary":null,"start":16438822,"end":16478678,"strand":1,"description":"LRRC75A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28619]"}, {"versioned_ensembl_gene_id":"ENSG00000273308.1","gene_symbol":"AC024560.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197645669,"end":197646017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196787.3","gene_symbol":"HIST1H2AG","gene_name":"histone cluster 1 H2A family member g [Source:HGNC Symbol;Acc:HGNC:4737]","synonyms":"pH2A/f,H2AFP,H2A/p,H2A.1b","biotype":"protein_coding","ncbi_id":"8969","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]","start":27133042,"end":27135291,"strand":1,"description":"histone cluster 1 H2A family member g [Source:HGNC Symbol;Acc:HGNC:4737]"}, {"versioned_ensembl_gene_id":"ENSG00000211724.3","gene_symbol":"TRBV6-6","gene_name":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]","synonyms":"TRBV66,TCRBV6S6,TCRBV13S6A2T","biotype":"TR_V_gene","ncbi_id":"28601","summary":null,"start":142469537,"end":142470013,"strand":1,"description":"T-cell receptor beta variable 6-6 [Source:HGNC Symbol;Acc:HGNC:12231]"}, {"versioned_ensembl_gene_id":"ENSG00000233060.1","gene_symbol":"AC016700.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70089721,"end":70096100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244617.2","gene_symbol":"ASPRV1","gene_name":"aspartic peptidase retroviral like 1 [Source:HGNC Symbol;Acc:HGNC:26321]","synonyms":"Taps,SASPase,FLJ25084","biotype":"protein_coding","ncbi_id":"151516","summary":"Filaggrin is a structural protein that is crucial for in the development and maintenance of the skin barrier. This gene encodes a retroviral-like protease involved in profilaggrin-to-filaggrin processing. Expression is found primarily in the epidermis and inner root sheath of hair follicles. [provided by RefSeq, May 2017]","start":69960089,"end":69962265,"strand":-1,"description":"aspartic peptidase retroviral like 1 [Source:HGNC Symbol;Acc:HGNC:26321]"}, {"versioned_ensembl_gene_id":"ENSG00000270826.1","gene_symbol":"Z94722.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93776911,"end":93777384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256847.1","gene_symbol":"CCND2P1","gene_name":"cyclin D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1584]","synonyms":"CCND2P","biotype":"processed_pseudogene","ncbi_id":"895","summary":null,"start":63243085,"end":63244004,"strand":1,"description":"cyclin D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1584]"}, {"versioned_ensembl_gene_id":"ENSG00000278632.5","gene_symbol":"TBC1D3B","gene_name":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]","synonyms":"TBC1D3I,PRC17,TBC1D3I,PRC17","biotype":"protein_coding","ncbi_id":"414059","summary":"This gene encodes a protein that is similar to TBC1 domain family, member 3. This protein contains a TBC (Tre-2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q. [provided by RefSeq, Apr 2009]","start":36253723,"end":36264678,"strand":-1,"description":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]"}, {"versioned_ensembl_gene_id":"ENSG00000114805.16","gene_symbol":"PLCH1","gene_name":"phospholipase C eta 1 [Source:HGNC Symbol;Acc:HGNC:29185]","synonyms":"PLCeta1,MGC117152,KIAA1069,DKFZp434C1372,PLCL3","biotype":"protein_coding","ncbi_id":"23007","summary":"PLCH1 is a member of the PLC-eta family of the phosphoinositide-specific phospholipase C (PLC) superfamily of enzymes that cleave phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) to generate second messengers inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) (Hwang et al., 2005 [PubMed 15702972]).[supplied by OMIM, Jun 2009]","start":155375580,"end":155745067,"strand":-1,"description":"phospholipase C eta 1 [Source:HGNC Symbol;Acc:HGNC:29185]"}, {"versioned_ensembl_gene_id":"ENSG00000243799.1","gene_symbol":"PEX5L-AS1","gene_name":"PEX5L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41251]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874040","summary":null,"start":179875376,"end":179881609,"strand":1,"description":"PEX5L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41251]"}, {"versioned_ensembl_gene_id":"ENSG00000281416.1","gene_symbol":"AC006359.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144561389,"end":144568027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133318.13","gene_symbol":"RTN3","gene_name":"reticulon 3 [Source:HGNC Symbol;Acc:HGNC:10469]","synonyms":"RTN3-A1,NSPL2,NSPLII,HAP,ASYIP","biotype":"protein_coding","ncbi_id":"10313","summary":"This gene belongs to the reticulon family of highly conserved genes that are preferentially expressed in neuroendocrine tissues. This family of proteins interact with, and modulate the activity of beta-amyloid converting enzyme 1 (BACE1), and the production of amyloid-beta. An increase in the expression of any reticulon protein substantially reduces the production of amyloid-beta, suggesting that reticulon proteins are negative modulators of BACE1 in cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, and pseudogenes of this gene are located on chromosomes 4 and 12. [provided by RefSeq, May 2012]","start":63681446,"end":63759891,"strand":1,"description":"reticulon 3 [Source:HGNC Symbol;Acc:HGNC:10469]"}, {"versioned_ensembl_gene_id":"ENSG00000220377.1","gene_symbol":"GSTA8P","gene_name":"glutathione S-transferase alpha 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:49903]","synonyms":"GSTAP7","biotype":"unprocessed_pseudogene","ncbi_id":"100420627","summary":null,"start":52687930,"end":52703825,"strand":-1,"description":"glutathione S-transferase alpha 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:49903]"}, {"versioned_ensembl_gene_id":"ENSG00000183580.9","gene_symbol":"FBXL7","gene_name":"F-box and leucine rich repeat protein 7 [Source:HGNC Symbol;Acc:HGNC:13604]","synonyms":"FBL6,KIAA0840,FBL7","biotype":"protein_coding","ncbi_id":"23194","summary":"This gene encodes a member of the F-box protein family which is characterized by a 42-48 amino acid motif, the F-box, which binds to the S-phase kinase-associated protein 1 (Skp1) protein. The F-box proteins constitute one of the four subunits of E3 ubiquitin protein ligases called SCFs (SKP1-Cul1-F-box), which play a role in phosphorylation-dependent ubiquitination of proteins. The F-box proteins are divided into 3 subfamilies based on the other domain in the protein: F-box proteins that also have a WD-40 domain (Fbws subfamily), F-box proteins that also have leucine-rich repeats (Fbls subfamily) and F-box proteins that contain other motifs or lack known protein-interaction domains (Fbxs subfamily). The protein encoded by this gene belongs to the Fbls subfamily. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":15500196,"end":15939795,"strand":1,"description":"F-box and leucine rich repeat protein 7 [Source:HGNC Symbol;Acc:HGNC:13604]"}, {"versioned_ensembl_gene_id":"ENSG00000243307.2","gene_symbol":"POM121L6P","gene_name":"POM121 transmembrane nucleoporin like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:31343]","synonyms":"bA239L20.2","biotype":"processed_pseudogene","ncbi_id":"729392","summary":null,"start":26896952,"end":26898777,"strand":1,"description":"POM121 transmembrane nucleoporin like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:31343]"}, {"versioned_ensembl_gene_id":"ENSG00000254394.1","gene_symbol":"AC105031.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82912104,"end":82961926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176463.13","gene_symbol":"SLCO3A1","gene_name":"solute carrier organic anion transporter family member 3A1 [Source:HGNC Symbol;Acc:HGNC:10952]","synonyms":"SLC21A11,OATP3A1,OATP-D","biotype":"protein_coding","ncbi_id":"28232","summary":null,"start":91853695,"end":92172435,"strand":1,"description":"solute carrier organic anion transporter family member 3A1 [Source:HGNC Symbol;Acc:HGNC:10952]"}, {"versioned_ensembl_gene_id":"ENSG00000253836.1","gene_symbol":"AC105031.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82862779,"end":82958696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227995.1","gene_symbol":"RAB11AP1","gene_name":"RAB11A, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45188]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129731","summary":null,"start":93881293,"end":93881938,"strand":-1,"description":"RAB11A, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45188]"}, {"versioned_ensembl_gene_id":"ENSG00000253570.1","gene_symbol":"AC069120.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38600661,"end":38601200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260661.1","gene_symbol":"AC116903.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92148752,"end":92331037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277649.2","gene_symbol":"TIMM22","gene_name":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]","synonyms":"TIM22,TEX4","biotype":"protein_coding","ncbi_id":"29928","summary":"Multipass transmembrane proteins are brought into mitochondria and inserted into the mitochondrial inner membrane by way of the TIM22 complex. This complex has six subunits and is a twin-pore translocase. The protein encoded by this gene is a subunit of TIM22 and represents the voltage-activated and signal-gated channel. [provided by RefSeq, Jul 2016]","start":997117,"end":1003671,"strand":1,"description":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]"}, {"versioned_ensembl_gene_id":"ENSG00000253503.5","gene_symbol":"AC060765.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82514568,"end":82677153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197016.11","gene_symbol":"ZNF470","gene_name":"zinc finger protein 470 [Source:HGNC Symbol;Acc:HGNC:22220]","synonyms":"FLJ26175,CZF-1","biotype":"protein_coding","ncbi_id":"388566","summary":null,"start":56567511,"end":56588911,"strand":1,"description":"zinc finger protein 470 [Source:HGNC Symbol;Acc:HGNC:22220]"}, {"versioned_ensembl_gene_id":"ENSG00000220248.1","gene_symbol":"ZNF402P","gene_name":"zinc finger protein 402, pseudogene [Source:HGNC Symbol;Acc:HGNC:19292]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266673","summary":null,"start":16857619,"end":16860718,"strand":-1,"description":"zinc finger protein 402, pseudogene [Source:HGNC Symbol;Acc:HGNC:19292]"}, {"versioned_ensembl_gene_id":"ENSG00000188313.12","gene_symbol":"PLSCR1","gene_name":"phospholipid scramblase 1 [Source:HGNC Symbol;Acc:HGNC:9092]","synonyms":"MMTRA1B","biotype":"protein_coding","ncbi_id":"5359","summary":null,"start":146515180,"end":146544864,"strand":-1,"description":"phospholipid scramblase 1 [Source:HGNC Symbol;Acc:HGNC:9092]"}, {"versioned_ensembl_gene_id":"ENSG00000274308.1","gene_symbol":"AC244093.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37140611,"end":37141424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230358.3","gene_symbol":"SPDYE21P","gene_name":"speedy/RINGO cell cycle regulator family member E21, pseudogene [Source:HGNC Symbol;Acc:HGNC:51517]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442572","summary":null,"start":67279778,"end":67286230,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E21, pseudogene [Source:HGNC Symbol;Acc:HGNC:51517]"}, {"versioned_ensembl_gene_id":"ENSG00000236488.1","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":33032931,"end":33033608,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000237835.1","gene_symbol":"AC007064.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16855804,"end":16856162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278505.4","gene_symbol":"C17orf78","gene_name":"chromosome 17 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:26831]","synonyms":"FLJ39647","biotype":"protein_coding","ncbi_id":"284099","summary":null,"start":37375986,"end":37392708,"strand":1,"description":"chromosome 17 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:26831]"}, {"versioned_ensembl_gene_id":"ENSG00000171163.15","gene_symbol":"ZNF692","gene_name":"zinc finger protein 692 [Source:HGNC Symbol;Acc:HGNC:26049]","synonyms":"Zfp692,FLJ20531,AREBP","biotype":"protein_coding","ncbi_id":"55657","summary":null,"start":248850006,"end":248859144,"strand":-1,"description":"zinc finger protein 692 [Source:HGNC Symbol;Acc:HGNC:26049]"}, {"versioned_ensembl_gene_id":"ENSG00000163362.10","gene_symbol":"INAVA","gene_name":"innate immunity activator [Source:HGNC Symbol;Acc:HGNC:25599]","synonyms":"FLJ10901,C1orf106","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":200891048,"end":200915735,"strand":1,"description":"innate immunity activator [Source:HGNC Symbol;Acc:HGNC:25599]"}, {"versioned_ensembl_gene_id":"ENSG00000244045.12","gene_symbol":"TMEM199","gene_name":"transmembrane protein 199 [Source:HGNC Symbol;Acc:HGNC:18085]","synonyms":"VPH2,VMA12,MGC45714,C17orf32","biotype":"protein_coding","ncbi_id":"147007","summary":"The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. The encoded protein shares some homology with the yeast protein Vma12. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. [provided by RefSeq, Mar 2016]","start":28357581,"end":28363683,"strand":1,"description":"transmembrane protein 199 [Source:HGNC Symbol;Acc:HGNC:18085]"}, {"versioned_ensembl_gene_id":"ENSG00000149435.12","gene_symbol":"GGTLC1","gene_name":"gamma-glutamyltransferase light chain 1 [Source:HGNC Symbol;Acc:HGNC:16437]","synonyms":"GGTLA4,GGTLA3,dJ831C21.2,dJ831C21.1","biotype":"protein_coding","ncbi_id":"92086","summary":"This gene encodes a member of the gamma-glutamyl transpeptidase (GGT) family, which are important in the metabolism of glutathione. The most ubiquitously expressed human GGT gene, GGT1, encodes a single transmembrane polypeptide that is post-translationally processed to form a heavy and a light chain. In contrast, the product of this gene only contains homology to the light chain region, and lacks a transmembrane domain. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2008]","start":23985050,"end":23988779,"strand":-1,"description":"gamma-glutamyltransferase light chain 1 [Source:HGNC Symbol;Acc:HGNC:16437]"}, {"versioned_ensembl_gene_id":"ENSG00000109158.10","gene_symbol":"GABRA4","gene_name":"gamma-aminobutyric acid type A receptor alpha4 subunit [Source:HGNC Symbol;Acc:HGNC:4078]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2557","summary":"Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. This gene encodes subunit alpha-4, which is involved in the etiology of autism and eventually increases autism risk through interaction with another subunit, gamma-aminobutyric acid receptor beta-1 (GABRB1). Alternatively spliced transcript variants encoding different isoforms have been found in this gene.[provided by RefSeq, Feb 2011]","start":46918900,"end":46994407,"strand":-1,"description":"gamma-aminobutyric acid type A receptor alpha4 subunit [Source:HGNC Symbol;Acc:HGNC:4078]"}, {"versioned_ensembl_gene_id":"ENSG00000259057.1","gene_symbol":"AC105109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91742841,"end":91743955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228223.3","gene_symbol":"HCG11","gene_name":"HLA complex group 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17707]","synonyms":"FLJ30357,FLJ14049,bK14H9.3","biotype":"lincRNA","ncbi_id":"493812","summary":null,"start":26521709,"end":26527404,"strand":1,"description":"HLA complex group 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17707]"}, {"versioned_ensembl_gene_id":"ENSG00000258765.1","gene_symbol":"AC107958.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91643017,"end":91649114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258551.5","gene_symbol":"CRAT37","gene_name":"cervical cancer-associated transcript 37 [Source:NCBI gene;Acc:101926928]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926928","summary":null,"start":91408708,"end":91605211,"strand":1,"description":"cervical cancer-associated transcript 37 [Source:NCBI gene;Acc:101926928]"}, {"versioned_ensembl_gene_id":"ENSG00000224356.5","gene_symbol":"AL356966.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":100535741,"end":100587146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226879.1","gene_symbol":"CR762479.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33057389,"end":33057798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233771.2","gene_symbol":"CICP5","gene_name":"capicua transcriptional repressor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37754]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"730978","summary":null,"start":223947605,"end":223950416,"strand":1,"description":"capicua transcriptional repressor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37754]"}, {"versioned_ensembl_gene_id":"ENSG00000239881.1","gene_symbol":"AC003982.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":120369440,"end":120371688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230137.1","gene_symbol":"AC004832.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30439837,"end":30440318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274950.4","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201424,"end":54249604,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000235816.3","gene_symbol":"PRELID1P3","gene_name":"PRELI domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420046","summary":null,"start":63427297,"end":63427939,"strand":1,"description":"PRELI domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43888]"}, {"versioned_ensembl_gene_id":"ENSG00000275280.1","gene_symbol":"AC007274.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7656968,"end":7657352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224412.1","gene_symbol":"AC022022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63489461,"end":63489638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057252.12","gene_symbol":"SOAT1","gene_name":"sterol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:11177]","synonyms":"SOAT,ACAT,STAT","biotype":"protein_coding","ncbi_id":"6646","summary":"The protein encoded by this gene belongs to the acyltransferase family. It is located in the endoplasmic reticulum, and catalyzes the formation of fatty acid-cholesterol esters. This gene has been implicated in the formation of beta-amyloid and atherosclerotic plaques by controlling the equilibrium between free cholesterol and cytoplasmic cholesteryl esters. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2011]","start":179293714,"end":179358680,"strand":1,"description":"sterol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:11177]"}, {"versioned_ensembl_gene_id":"ENSG00000137941.16","gene_symbol":"TTLL7","gene_name":"tubulin tyrosine ligase like 7 [Source:HGNC Symbol;Acc:HGNC:26242]","synonyms":"FLJ23033","biotype":"protein_coding","ncbi_id":"79739","summary":null,"start":83865028,"end":83999150,"strand":-1,"description":"tubulin tyrosine ligase like 7 [Source:HGNC Symbol;Acc:HGNC:26242]"}, {"versioned_ensembl_gene_id":"ENSG00000214265.11","gene_symbol":"AC124312.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24955034,"end":25000276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064989.12","gene_symbol":"CALCRL","gene_name":"calcitonin receptor like receptor [Source:HGNC Symbol;Acc:HGNC:16709]","synonyms":"CRLR,CGRPR","biotype":"protein_coding","ncbi_id":"10203","summary":null,"start":187343129,"end":187448460,"strand":-1,"description":"calcitonin receptor like receptor [Source:HGNC Symbol;Acc:HGNC:16709]"}, {"versioned_ensembl_gene_id":"ENSG00000249936.3","gene_symbol":"RAC1P2","gene_name":"ras-related C3 botulinum toxin substrate 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31414]","synonyms":"Psi2Rac1","biotype":"processed_pseudogene","ncbi_id":"442775","summary":null,"start":46723830,"end":46724408,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31414]"}, {"versioned_ensembl_gene_id":"ENSG00000196110.7","gene_symbol":"ZNF699","gene_name":"zinc finger protein 699 [Source:HGNC Symbol;Acc:HGNC:24750]","synonyms":"hang,FLJ38144","biotype":"protein_coding","ncbi_id":"374879","summary":null,"start":9294275,"end":9309838,"strand":-1,"description":"zinc finger protein 699 [Source:HGNC Symbol;Acc:HGNC:24750]"}, {"versioned_ensembl_gene_id":"ENSG00000262052.1","gene_symbol":"AC090618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55842677,"end":55872939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272592.1","gene_symbol":"AL451049.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61684892,"end":61685388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234798.6","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31962464,"end":31964946,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000251321.1","gene_symbol":"PCAT4","gene_name":"prostate cancer associated transcript 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:24853]","synonyms":"PCAN1,PCA4,GDEP","biotype":"lincRNA","ncbi_id":"118425","summary":null,"start":79827471,"end":79877770,"strand":1,"description":"prostate cancer associated transcript 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:24853]"}, {"versioned_ensembl_gene_id":"ENSG00000100365.14","gene_symbol":"NCF4","gene_name":"neutrophil cytosolic factor 4 [Source:HGNC Symbol;Acc:HGNC:7662]","synonyms":"SH3PXD4,p40phox","biotype":"protein_coding","ncbi_id":"4689","summary":"The protein encoded by this gene is a cytosolic regulatory component of the superoxide-producing phagocyte NADPH-oxidase, a multicomponent enzyme system important for host defense. This protein is preferentially expressed in cells of myeloid lineage. It interacts primarily with neutrophil cytosolic factor 2 (NCF2/p67-phox) to form a complex with neutrophil cytosolic factor 1 (NCF1/p47-phox), which further interacts with the small G protein RAC1 and translocates to the membrane upon cell stimulation. This complex then activates flavocytochrome b, the membrane-integrated catalytic core of the enzyme system. The PX domain of this protein can bind phospholipid products of the PI(3) kinase, which suggests its role in PI(3) kinase-mediated signaling events. The phosphorylation of this protein was found to negatively regulate the enzyme activity. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":36860988,"end":36878015,"strand":1,"description":"neutrophil cytosolic factor 4 [Source:HGNC Symbol;Acc:HGNC:7662]"}, {"versioned_ensembl_gene_id":"ENSG00000058804.11","gene_symbol":"NDC1","gene_name":"NDC1 transmembrane nucleoporin [Source:HGNC Symbol;Acc:HGNC:25525]","synonyms":"NET3,FLJ10407,TMEM48","biotype":"protein_coding","ncbi_id":"55706","summary":null,"start":53765460,"end":53838860,"strand":-1,"description":"NDC1 transmembrane nucleoporin [Source:HGNC Symbol;Acc:HGNC:25525]"}, {"versioned_ensembl_gene_id":"ENSG00000282337.1","gene_symbol":"IGHV1-58","gene_name":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28464","summary":null,"start":106647038,"end":106647536,"strand":-1,"description":"immunoglobulin heavy variable 1-58 [Source:HGNC Symbol;Acc:HGNC:5555]"}, {"versioned_ensembl_gene_id":"ENSG00000225726.1","gene_symbol":"AC007000.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77071751,"end":77072237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262158.1","gene_symbol":"MTCO3P24","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52127]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075217","summary":null,"start":10723836,"end":10724617,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:52127]"}, {"versioned_ensembl_gene_id":"ENSG00000279630.1","gene_symbol":"AC190387.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":109020833,"end":109021240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276913.2","gene_symbol":"C17orf98","gene_name":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]","synonyms":"LOC388381","biotype":"protein_coding","ncbi_id":"388381","summary":null,"start":38635875,"end":38642242,"strand":-1,"description":"chromosome 17 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:34492]"}, {"versioned_ensembl_gene_id":"ENSG00000230678.10","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"RING3,BRD2-IT1,FSRG1,NAT,D6S113E,KIAA9001","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":32955787,"end":32959446,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000205208.4","gene_symbol":"C4orf46","gene_name":"chromosome 4 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:27320]","synonyms":"RCDG1,LOC201725","biotype":"protein_coding","ncbi_id":"201725","summary":"This gene encodes a small, conserved protein of unknown function that is expressed in a variety of tissues. There are pseudogenes for this gene on chromosomes 6, 8, 16, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":158666679,"end":158672255,"strand":-1,"description":"chromosome 4 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:27320]"}, {"versioned_ensembl_gene_id":"ENSG00000217083.1","gene_symbol":"MTCO2P33","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52162]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075197","summary":null,"start":24947880,"end":24948344,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52162]"}, {"versioned_ensembl_gene_id":"ENSG00000271275.1","gene_symbol":"AC007326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18997138,"end":18997595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083750.12","gene_symbol":"RRAGB","gene_name":"Ras related GTP binding B [Source:HGNC Symbol;Acc:HGNC:19901]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10325","summary":"Ras-homologous GTPases constitute a large family of signal transducers that alternate between an activated, GTP-binding state and an inactivated, GDP-binding state. These proteins represent cellular switches that are operated by GTP-exchange factors and factors that stimulate their intrinsic GTPase activity. All GTPases of the Ras superfamily have in common the presence of six conserved motifs involved in GTP/GDP binding, three of which are phosphate-/magnesium-binding sites (PM1-PM3) and three of which are guanine nucleotide-binding sites (G1-G3). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":55717739,"end":55758774,"strand":1,"description":"Ras related GTP binding B [Source:HGNC Symbol;Acc:HGNC:19901]"}, {"versioned_ensembl_gene_id":"ENSG00000260286.3","gene_symbol":"C6orf229","gene_name":"chromosome 6 open reading frame 229 [Source:HGNC Symbol;Acc:HGNC:49394]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928603","summary":null,"start":24797321,"end":24798889,"strand":-1,"description":"chromosome 6 open reading frame 229 [Source:HGNC Symbol;Acc:HGNC:49394]"}, {"versioned_ensembl_gene_id":"ENSG00000180543.4","gene_symbol":"TSPYL5","gene_name":"TSPY like 5 [Source:HGNC Symbol;Acc:HGNC:29367]","synonyms":"KIAA1750","biotype":"protein_coding","ncbi_id":"85453","summary":null,"start":97273474,"end":97277964,"strand":-1,"description":"TSPY like 5 [Source:HGNC Symbol;Acc:HGNC:29367]"}, {"versioned_ensembl_gene_id":"ENSG00000267231.1","gene_symbol":"AC005786.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3558015,"end":3558486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230361.1","gene_symbol":"VN1R32P","gene_name":"vomeronasal 1 receptor 32 pseudogene [Source:HGNC Symbol;Acc:HGNC:37352]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100312788","summary":null,"start":63377329,"end":63378233,"strand":1,"description":"vomeronasal 1 receptor 32 pseudogene [Source:HGNC Symbol;Acc:HGNC:37352]"}, {"versioned_ensembl_gene_id":"ENSG00000126524.9","gene_symbol":"SBDS","gene_name":"SBDS, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:19440]","synonyms":"SWDS,SDS,FLJ10917,CGI-97","biotype":"protein_coding","ncbi_id":"51119","summary":"This gene encodes a highly conserved protein that plays an essential role in ribosome biogenesis. The encoded protein interacts with elongation factor-like GTPase 1 to disassociate eukaryotic initiation factor 6 from the late cytoplasmic pre-60S ribosomal subunit allowing assembly of the 80S subunit. Mutations within this gene are associated with the autosomal recessive disorder Shwachman-Bodian-Diamond syndrome. This gene has a closely linked pseudogene that is distally located. [provided by RefSeq, Jan 2017]","start":66987677,"end":66995601,"strand":-1,"description":"SBDS, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:19440]"}, {"versioned_ensembl_gene_id":"ENSG00000231942.3","gene_symbol":"HNRNPA1P36","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:48765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128836","summary":null,"start":81807772,"end":81808726,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:48765]"}, {"versioned_ensembl_gene_id":"ENSG00000250564.1","gene_symbol":"AC109454.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134429051,"end":134460615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171503.11","gene_symbol":"ETFDH","gene_name":"electron transfer flavoprotein dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3483]","synonyms":"ETFQO","biotype":"protein_coding","ncbi_id":"2110","summary":"This gene encodes a component of the electron-transfer system in mitochondria and is essential for electron transfer from a number of mitochondrial flavin-containing dehydrogenases to the main respiratory chain. Mutations in this gene are associated with glutaric acidemia. Alternatively spliced transcript variants that encode distinct isoforms have been observed. [provided by RefSeq, Aug 2013]","start":158672125,"end":158709623,"strand":1,"description":"electron transfer flavoprotein dehydrogenase [Source:HGNC Symbol;Acc:HGNC:3483]"}, {"versioned_ensembl_gene_id":"ENSG00000068784.12","gene_symbol":"SRBD1","gene_name":"S1 RNA binding domain 1 [Source:HGNC Symbol;Acc:HGNC:25521]","synonyms":"FLJ10379","biotype":"protein_coding","ncbi_id":"55133","summary":null,"start":45388680,"end":45612165,"strand":-1,"description":"S1 RNA binding domain 1 [Source:HGNC Symbol;Acc:HGNC:25521]"}, {"versioned_ensembl_gene_id":"ENSG00000100362.12","gene_symbol":"PVALB","gene_name":"parvalbumin [Source:HGNC Symbol;Acc:HGNC:9704]","synonyms":"D22S749","biotype":"protein_coding","ncbi_id":"5816","summary":"The protein encoded by this gene is a high affinity calcium ion-binding protein that is structurally and functionally similar to calmodulin and troponin C. The encoded protein is thought to be involved in muscle relaxation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":36800684,"end":36819479,"strand":-1,"description":"parvalbumin [Source:HGNC Symbol;Acc:HGNC:9704]"}, {"versioned_ensembl_gene_id":"ENSG00000261609.5","gene_symbol":"GAN","gene_name":"gigaxonin [Source:HGNC Symbol;Acc:HGNC:4137]","synonyms":"KLHL16,GAN1","biotype":"protein_coding","ncbi_id":"8139","summary":"This gene encodes a member of the cytoskeletal BTB/kelch (Broad-Complex, Tramtrack and Bric a brac) repeat family. The encoded protein plays a role in neurofilament architecture and is involved in mediating the ubiquitination and degradation of some proteins. Defects in this gene are a cause of giant axonal neuropathy (GAN). [provided by RefSeq, Oct 2008]","start":81314952,"end":81390884,"strand":1,"description":"gigaxonin [Source:HGNC Symbol;Acc:HGNC:4137]"}, {"versioned_ensembl_gene_id":"ENSG00000228505.5","gene_symbol":"AC011897.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14616428,"end":14630192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187185.4","gene_symbol":"AC092118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57798186,"end":57816946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103707.9","gene_symbol":"MTFMT","gene_name":"mitochondrial methionyl-tRNA formyltransferase [Source:HGNC Symbol;Acc:HGNC:29666]","synonyms":"FMT1","biotype":"protein_coding","ncbi_id":"123263","summary":"The protein encoded by this nuclear gene localizes to the mitochondrion, where it catalyzes the formylation of methionyl-tRNA. [provided by RefSeq, Jun 2011]","start":65001512,"end":65029639,"strand":-1,"description":"mitochondrial methionyl-tRNA formyltransferase [Source:HGNC Symbol;Acc:HGNC:29666]"}, {"versioned_ensembl_gene_id":"ENSG00000275315.1","gene_symbol":"AC141273.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20616409,"end":20616532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228367.3","gene_symbol":"AC108120.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75920670,"end":75921660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262259.1","gene_symbol":"MTND4LP24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42258]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075103","summary":null,"start":10723065,"end":10723355,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42258]"}, {"versioned_ensembl_gene_id":"ENSG00000115353.10","gene_symbol":"TACR1","gene_name":"tachykinin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11526]","synonyms":"TAC1R,SPR,NKIR,NK1R","biotype":"protein_coding","ncbi_id":"6869","summary":"This gene belongs to a gene family of tachykinin receptors. These tachykinin receptors are characterized by interactions with G proteins and contain seven hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin substance P, also referred to as neurokinin 1. The encoded protein is also involved in the mediation of phosphatidylinositol metabolism of substance P. [provided by RefSeq, Sep 2008]","start":75046463,"end":75199700,"strand":-1,"description":"tachykinin receptor 1 [Source:HGNC Symbol;Acc:HGNC:11526]"}, {"versioned_ensembl_gene_id":"ENSG00000228267.8","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"CO4,C4B3,CH,C4B1,CPAMD3,C4F","biotype":"protein_coding","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":31969570,"end":31983859,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000282457.1","gene_symbol":"CSPG4P10","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48361]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390627","summary":null,"start":82538538,"end":82556321,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48361]"}, {"versioned_ensembl_gene_id":"ENSG00000231039.2","gene_symbol":"AL355303.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5234358,"end":5263408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213402.2","gene_symbol":"PTPRCAP","gene_name":"protein tyrosine phosphatase, receptor type C associated protein [Source:HGNC Symbol;Acc:HGNC:9667]","synonyms":"CD45-AP,LPAP","biotype":"protein_coding","ncbi_id":"5790","summary":"The protein encoded by this gene was identified as a transmembrane phosphoprotein specifically associated with tyrosine phosphatase PTPRC/CD45, a key regulator of T- and B-lymphocyte activation. The interaction with PTPRC may be required for the stable expression of this protein. [provided by RefSeq, Jul 2008]","start":67435510,"end":67438067,"strand":-1,"description":"protein tyrosine phosphatase, receptor type C associated protein [Source:HGNC Symbol;Acc:HGNC:9667]"}, {"versioned_ensembl_gene_id":"ENSG00000270117.1","gene_symbol":"AP000769.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65498010,"end":65498405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227102.2","gene_symbol":"OR2AS1P","gene_name":"olfactory receptor family 2 subfamily AS member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15004]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248549444,"end":248549762,"strand":-1,"description":"olfactory receptor family 2 subfamily AS member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15004]"}, {"versioned_ensembl_gene_id":"ENSG00000005249.12","gene_symbol":"PRKAR2B","gene_name":"protein kinase cAMP-dependent type II regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9392]","synonyms":"PRKAR2","biotype":"protein_coding","ncbi_id":"5577","summary":"cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. The protein encoded by this gene is one of the regulatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. This subunit has been shown to interact with and suppress the transcriptional activity of the cAMP responsive element binding protein 1 (CREB1) in activated T cells. Knockout studies in mice suggest that this subunit may play an important role in regulating energy balance and adiposity. The studies also suggest that this subunit may mediate the gene induction and cataleptic behavior induced by haloperidol. [provided by RefSeq, Jul 2008]","start":107044649,"end":107161811,"strand":1,"description":"protein kinase cAMP-dependent type II regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9392]"}, {"versioned_ensembl_gene_id":"ENSG00000277516.1","gene_symbol":"AL590410.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55520382,"end":55520714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273734.1","gene_symbol":"AC005258.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2269525,"end":2341172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244541.5","gene_symbol":"LINC01213","gene_name":"long intergenic non-protein coding RNA 1213 [Source:HGNC Symbol;Acc:HGNC:49648]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927992","summary":null,"start":150238519,"end":150240209,"strand":1,"description":"long intergenic non-protein coding RNA 1213 [Source:HGNC Symbol;Acc:HGNC:49648]"}, {"versioned_ensembl_gene_id":"ENSG00000100167.19","gene_symbol":"SEPT3","gene_name":"septin 3 [Source:HGNC Symbol;Acc:HGNC:10750]","synonyms":"SEP3","biotype":"protein_coding","ncbi_id":"55964","summary":"This gene belongs to the septin family of GTPases. Members of this family are required for cytokinesis. Expression is upregulated by retinoic acid in a human teratocarcinoma cell line. The specific function of this gene has not been determined. Alternative splicing of this gene results in several transcript variants encoding different isoforms. [provided by RefSeq, May 2018]","start":41976272,"end":41998221,"strand":1,"description":"septin 3 [Source:HGNC Symbol;Acc:HGNC:10750]"}, {"versioned_ensembl_gene_id":"ENSG00000277988.1","gene_symbol":"FAM30B","gene_name":"family with sequence similarity 30 member B [Source:HGNC Symbol;Acc:HGNC:31023]","synonyms":"KIAA0125P1,HsT16028","biotype":"unprocessed_pseudogene","ncbi_id":"105379202","summary":null,"start":20012741,"end":20014208,"strand":1,"description":"family with sequence similarity 30 member B [Source:HGNC Symbol;Acc:HGNC:31023]"}, {"versioned_ensembl_gene_id":"ENSG00000259769.1","gene_symbol":"AC127381.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20046296,"end":20047994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267145.1","gene_symbol":"AC006116.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56338288,"end":56338648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184608.8","gene_symbol":"FAM167A-AS1","gene_name":"FAM167A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:15548]","synonyms":"C8orf12","biotype":"antisense_RNA","ncbi_id":"83656","summary":null,"start":11368402,"end":11438658,"strand":1,"description":"FAM167A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:15548]"}, {"versioned_ensembl_gene_id":"ENSG00000141052.17","gene_symbol":"MYOCD","gene_name":"myocardin [Source:HGNC Symbol;Acc:HGNC:16067]","synonyms":"MYCD","biotype":"protein_coding","ncbi_id":"93649","summary":"This gene encodes a nuclear protein, which is expressed in heart, aorta, and in smooth muscle cell-containing tissues. It functions as a transcriptional co-activator of serum response factor (SRF) and modulates expression of cardiac and smooth muscle-specific SRF-target genes, and thus may play a crucial role in cardiogenesis and differentiation of the smooth muscle cell lineage. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":12665890,"end":12768949,"strand":1,"description":"myocardin [Source:HGNC Symbol;Acc:HGNC:16067]"}, {"versioned_ensembl_gene_id":"ENSG00000188223.9","gene_symbol":"AD000671.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35745678,"end":35754519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256706.1","gene_symbol":"AC005342.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1917951,"end":1922867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140543.14","gene_symbol":"DET1","gene_name":"de-etiolated homolog 1 (Arabidopsis) [Source:HGNC Symbol;Acc:HGNC:25477]","synonyms":"FLJ10103","biotype":"protein_coding","ncbi_id":"55070","summary":null,"start":88494440,"end":88546675,"strand":-1,"description":"de-etiolated homolog 1 (Arabidopsis) [Source:HGNC Symbol;Acc:HGNC:25477]"}, {"versioned_ensembl_gene_id":"ENSG00000268988.1","gene_symbol":"SPANXN2","gene_name":"SPANX family member N2 [Source:HGNC Symbol;Acc:HGNC:33175]","synonyms":"SPANX-N2,CT11.7","biotype":"protein_coding","ncbi_id":"494119","summary":null,"start":143711955,"end":143721423,"strand":-1,"description":"SPANX family member N2 [Source:HGNC Symbol;Acc:HGNC:33175]"}, {"versioned_ensembl_gene_id":"ENSG00000277669.1","gene_symbol":"AC009086.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29663279,"end":29695144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271959.1","gene_symbol":"AC100803.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141434545,"end":141437954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259976.3","gene_symbol":"AC093010.3","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":114314501,"end":114329714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169508.6","gene_symbol":"GPR183","gene_name":"G protein-coupled receptor 183 [Source:HGNC Symbol;Acc:HGNC:3128]","synonyms":"EBI2","biotype":"protein_coding","ncbi_id":"1880","summary":"This gene was identified by the up-regulation of its expression upon Epstein-Barr virus infection of primary B lymphocytes. This gene is predicted to encode a G protein-coupled receptor that is most closely related to the thrombin receptor. Expression of this gene was detected in B-lymphocyte cell lines and lymphoid tissues but not in T-lymphocyte cell lines or peripheral blood T lymphocytes. The function of this gene is unknown. [provided by RefSeq, Jul 2008]","start":99294530,"end":99307405,"strand":-1,"description":"G protein-coupled receptor 183 [Source:HGNC Symbol;Acc:HGNC:3128]"}, {"versioned_ensembl_gene_id":"ENSG00000144354.13","gene_symbol":"CDCA7","gene_name":"cell division cycle associated 7 [Source:HGNC Symbol;Acc:HGNC:14628]","synonyms":"JPO1,FLJ14736","biotype":"protein_coding","ncbi_id":"83879","summary":"This gene was identified as a c-Myc responsive gene, and behaves as a direct c-Myc target gene. Overexpression of this gene is found to enhance the transformation of lymphoblastoid cells, and it complements a transformation-defective Myc Box II mutant, suggesting its involvement in c-Myc-mediated cell transformation. Two alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":173354820,"end":173368997,"strand":1,"description":"cell division cycle associated 7 [Source:HGNC Symbol;Acc:HGNC:14628]"}, {"versioned_ensembl_gene_id":"ENSG00000261627.1","gene_symbol":"AP005205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6641971,"end":6642478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205054.6","gene_symbol":"LINC01121","gene_name":"long intergenic non-protein coding RNA 1121 [Source:HGNC Symbol;Acc:HGNC:49266]","synonyms":"UNQ6975","biotype":"processed_transcript","ncbi_id":"400952","summary":null,"start":45164870,"end":45323295,"strand":-1,"description":"long intergenic non-protein coding RNA 1121 [Source:HGNC Symbol;Acc:HGNC:49266]"}, {"versioned_ensembl_gene_id":"ENSG00000231054.1","gene_symbol":"AC093833.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45168583,"end":45169414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232149.1","gene_symbol":"FERP1","gene_name":"FER tyrosine kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26443]","synonyms":"FERps,FERP","biotype":"processed_pseudogene","ncbi_id":"553112","summary":null,"start":123603139,"end":123603931,"strand":1,"description":"FER tyrosine kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26443]"}, {"versioned_ensembl_gene_id":"ENSG00000178814.16","gene_symbol":"OPLAH","gene_name":"5-oxoprolinase (ATP-hydrolysing) [Source:HGNC Symbol;Acc:HGNC:8149]","synonyms":"OPLA,5-Opase","biotype":"protein_coding","ncbi_id":"26873","summary":"The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]","start":144051266,"end":144063965,"strand":-1,"description":"5-oxoprolinase (ATP-hydrolysing) [Source:HGNC Symbol;Acc:HGNC:8149]"}, {"versioned_ensembl_gene_id":"ENSG00000205485.13","gene_symbol":"AC004980.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76549360,"end":76627982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141837.19","gene_symbol":"CACNA1A","gene_name":"calcium voltage-gated channel subunit alpha1 A [Source:HGNC Symbol;Acc:HGNC:1388]","synonyms":"Cav2.1,CACNL1A4,APCA,SCA6,MHP1,MHP,HPCA,FHM,EA2","biotype":"protein_coding","ncbi_id":"773","summary":"Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas, the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1A subunit, which is predominantly expressed in neuronal tissue. Mutations in this gene are associated with 2 neurologic disorders, familial hemiplegic migraine and episodic ataxia 2. This gene also exhibits polymorphic variation due to (CAG)n-repeats. Multiple transcript variants encoding different isoforms have been found for this gene. In one set of transcript variants, the (CAG)n-repeats occur in the 3' UTR, and are not associated with any disease. But in another set of variants, an insertion extends the coding region to include the (CAG)n-repeats which encode a polyglutamine tract. Expansion of the (CAG)n-repeats from the normal 4-18 to 21-33 in the coding region is associated with spinocerebellar ataxia 6. [provided by RefSeq, Jul 2016]","start":13206442,"end":13633025,"strand":-1,"description":"calcium voltage-gated channel subunit alpha1 A [Source:HGNC Symbol;Acc:HGNC:1388]"}, {"versioned_ensembl_gene_id":"ENSG00000242365.1","gene_symbol":"NDUFA5P5","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48847]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130327","summary":null,"start":88601061,"end":88601402,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48847]"}, {"versioned_ensembl_gene_id":"ENSG00000282533.1","gene_symbol":"AC244452.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106461096,"end":106461236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185201.16","gene_symbol":"IFITM2","gene_name":"interferon induced transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:5413]","synonyms":"1-8D","biotype":"protein_coding","ncbi_id":"10581","summary":null,"start":307631,"end":315272,"strand":1,"description":"interferon induced transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:5413]"}, {"versioned_ensembl_gene_id":"ENSG00000224227.3","gene_symbol":"OR2L1P","gene_name":"olfactory receptor family 2 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8265]","synonyms":"OR2L7P,OR2L1,HTPCRX02,HSHTPCRX02","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26247","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247980872,"end":247991204,"strand":1,"description":"olfactory receptor family 2 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8265]"}, {"versioned_ensembl_gene_id":"ENSG00000232215.2","gene_symbol":"OR2L6P","gene_name":"olfactory receptor family 2 subfamily L member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15012]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81465","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248003129,"end":248004068,"strand":1,"description":"olfactory receptor family 2 subfamily L member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15012]"}, {"versioned_ensembl_gene_id":"ENSG00000225661.7","gene_symbol":"RPL14P5","gene_name":"ribosomal protein L14 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442442","summary":null,"start":1008503,"end":1010101,"strand":-1,"description":"ribosomal protein L14 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37720]"}, {"versioned_ensembl_gene_id":"ENSG00000231286.7","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"HLA-DQB,CELIAC1,IDDM1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32690241,"end":32699289,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000259548.1","gene_symbol":"AC021483.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79832466,"end":79833554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132153.14","gene_symbol":"DHX30","gene_name":"DExH-box helicase 30 [Source:HGNC Symbol;Acc:HGNC:16716]","synonyms":"KIAA0890,FLJ11214,DDX30","biotype":"protein_coding","ncbi_id":"22907","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The family member encoded by this gene is a mitochondrial nucleoid protein that associates with mitochondrial DNA. It has also been identified as a component of a transcriptional repressor complex that functions in retinal development, and it is required to optimize the function of the zinc-finger antiviral protein. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]","start":47802909,"end":47850195,"strand":1,"description":"DExH-box helicase 30 [Source:HGNC Symbol;Acc:HGNC:16716]"}, {"versioned_ensembl_gene_id":"ENSG00000168734.13","gene_symbol":"PKIG","gene_name":"cAMP-dependent protein kinase inhibitor gamma [Source:HGNC Symbol;Acc:HGNC:9019]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11142","summary":"This gene encodes a member of the protein kinase inhibitor family. Studies of a similar protein in mice suggest that this protein acts as a potent competitive cAMP-dependent protein kinase inhibitor, and is a predominant form of inhibitor in various tissues. The encoded protein may be involved in osteogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":44531785,"end":44624247,"strand":1,"description":"cAMP-dependent protein kinase inhibitor gamma [Source:HGNC Symbol;Acc:HGNC:9019]"}, {"versioned_ensembl_gene_id":"ENSG00000258086.1","gene_symbol":"AC079313.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54353792,"end":54466985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258137.5","gene_symbol":"AC079313.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54353661,"end":54497688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144227.4","gene_symbol":"NXPH2","gene_name":"neurexophilin 2 [Source:HGNC Symbol;Acc:HGNC:8076]","synonyms":"NPH2","biotype":"protein_coding","ncbi_id":"11249","summary":null,"start":138670772,"end":138780348,"strand":-1,"description":"neurexophilin 2 [Source:HGNC Symbol;Acc:HGNC:8076]"}, {"versioned_ensembl_gene_id":"ENSG00000237772.1","gene_symbol":"AC092620.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138604510,"end":138613167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238226.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32811737,"end":32812588,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000168036.16","gene_symbol":"CTNNB1","gene_name":"catenin beta 1 [Source:HGNC Symbol;Acc:HGNC:2514]","synonyms":"CTNNB,beta-catenin,armadillo","biotype":"protein_coding","ncbi_id":"1499","summary":"The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":41194837,"end":41260096,"strand":1,"description":"catenin beta 1 [Source:HGNC Symbol;Acc:HGNC:2514]"}, {"versioned_ensembl_gene_id":"ENSG00000229286.1","gene_symbol":"AP000522.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15901791,"end":15901911,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074527.11","gene_symbol":"NTN4","gene_name":"netrin 4 [Source:HGNC Symbol;Acc:HGNC:13658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59277","summary":"This gene encodes a member of the netrin family of proteins, which function in various biological processes including axon guidance, tumorogenesis, and angiogenesis. Netrins are laminin-related proteins that have an N-terminal laminin-type domain, epidermal growth factor-like repeat domain, and a positively charged heparin-binding domain at the C-terminus. The protein encoded by this gene is involved in processes including neurite growth and migration, angiogenesis and mural cell adhesion to endothelial cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":95657807,"end":95791152,"strand":-1,"description":"netrin 4 [Source:HGNC Symbol;Acc:HGNC:13658]"}, {"versioned_ensembl_gene_id":"ENSG00000005844.17","gene_symbol":"ITGAL","gene_name":"integrin subunit alpha L [Source:HGNC Symbol;Acc:HGNC:6148]","synonyms":"LFA-1,CD11A","biotype":"protein_coding","ncbi_id":"3683","summary":"ITGAL encodes the integrin alpha L chain. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form the integrin lymphocyte function-associated antigen-1 (LFA-1), which is expressed on all leukocytes. LFA-1 plays a central role in leukocyte intercellular adhesion through interactions with its ligands, ICAMs 1-3 (intercellular adhesion molecules 1 through 3), and also functions in lymphocyte costimulatory signaling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30472658,"end":30523185,"strand":1,"description":"integrin subunit alpha L [Source:HGNC Symbol;Acc:HGNC:6148]"}, {"versioned_ensembl_gene_id":"ENSG00000275255.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786292,"end":54798222,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000125459.14","gene_symbol":"MSTO1","gene_name":"misato 1, mitochondrial distribution and morphology regulator [Source:HGNC Symbol;Acc:HGNC:29678]","synonyms":"misato,LST005,FLJ10504,MST","biotype":"protein_coding","ncbi_id":"55154","summary":null,"start":155610205,"end":155614967,"strand":1,"description":"misato 1, mitochondrial distribution and morphology regulator [Source:HGNC Symbol;Acc:HGNC:29678]"}, {"versioned_ensembl_gene_id":"ENSG00000275351.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832726,"end":54848250,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000248640.1","gene_symbol":"HNRNPA1P56","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:48786]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391670","summary":null,"start":77987860,"end":77988813,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:48786]"}, {"versioned_ensembl_gene_id":"ENSG00000228043.5","gene_symbol":"AC114763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138418284,"end":138501698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174255.6","gene_symbol":"ZNF80","gene_name":"zinc finger protein 80 [Source:HGNC Symbol;Acc:HGNC:13155]","synonyms":"pT17","biotype":"protein_coding","ncbi_id":"7634","summary":null,"start":114234631,"end":114237578,"strand":-1,"description":"zinc finger protein 80 [Source:HGNC Symbol;Acc:HGNC:13155]"}, {"versioned_ensembl_gene_id":"ENSG00000249901.1","gene_symbol":"AC121161.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158490766,"end":158509908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021461.16","gene_symbol":"CYP3A43","gene_name":"cytochrome P450 family 3 subfamily A member 43 [Source:HGNC Symbol;Acc:HGNC:17450]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64816","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein has a low level of testosterone hydroxylase activity, and may play a role in aging mechanisms and cancer progression. This gene is part of a cluster of cytochrome P450 genes on chromosome 7q21.1. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":99828013,"end":99866102,"strand":1,"description":"cytochrome P450 family 3 subfamily A member 43 [Source:HGNC Symbol;Acc:HGNC:17450]"}, {"versioned_ensembl_gene_id":"ENSG00000256751.5","gene_symbol":"PLBD1-AS1","gene_name":"PLBD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51143]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928290","summary":null,"start":14567750,"end":14619755,"strand":1,"description":"PLBD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51143]"}, {"versioned_ensembl_gene_id":"ENSG00000168273.7","gene_symbol":"SMIM4","gene_name":"small integral membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:37257]","synonyms":"C3orf78","biotype":"protein_coding","ncbi_id":"440957","summary":null,"start":52534013,"end":52579237,"strand":1,"description":"small integral membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:37257]"}, {"versioned_ensembl_gene_id":"ENSG00000231654.1","gene_symbol":"RPS6KA2-AS1","gene_name":"RPS6KA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40511]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861523","summary":null,"start":166903698,"end":166904835,"strand":1,"description":"RPS6KA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40511]"}, {"versioned_ensembl_gene_id":"ENSG00000270584.1","gene_symbol":"AC093813.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156263547,"end":156263802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281345.1","gene_symbol":"IGLV2-33","gene_name":"immunoglobulin lambda variable 2-33 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5892]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28811","summary":null,"start":22597260,"end":22597793,"strand":1,"description":"immunoglobulin lambda variable 2-33 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5892]"}, {"versioned_ensembl_gene_id":"ENSG00000230247.2","gene_symbol":"HNRNPH3P1","gene_name":"heterogeneous nuclear ribonucleoprotein H3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48750]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480233","summary":null,"start":80529037,"end":80530027,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein H3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48750]"}, {"versioned_ensembl_gene_id":"ENSG00000282655.1","gene_symbol":"PDCD6IPP2","gene_name":"PDCD6IP pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49873]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646278","summary":null,"start":28931169,"end":28943001,"strand":1,"description":"PDCD6IP pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49873]"}, {"versioned_ensembl_gene_id":"ENSG00000257853.2","gene_symbol":"MED15P1","gene_name":"mediator complex subunit 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19271]","synonyms":"PCQAPP,MED15P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"326615","summary":null,"start":18912805,"end":18916642,"strand":-1,"description":"mediator complex subunit 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19271]"}, {"versioned_ensembl_gene_id":"ENSG00000169288.17","gene_symbol":"MRPL1","gene_name":"mitochondrial ribosomal protein L1 [Source:HGNC Symbol;Acc:HGNC:14275]","synonyms":"BM022","biotype":"protein_coding","ncbi_id":"65008","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L1 ribosomal protein family. [provided by RefSeq, Jul 2008]","start":77862520,"end":77952790,"strand":1,"description":"mitochondrial ribosomal protein L1 [Source:HGNC Symbol;Acc:HGNC:14275]"}, {"versioned_ensembl_gene_id":"ENSG00000236259.1","gene_symbol":"AC017083.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68125265,"end":68125747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229292.1","gene_symbol":"RFPL4AL1","gene_name":"ret finger protein like 4A like 1 [Source:HGNC Symbol;Acc:HGNC:45147]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729974","summary":null,"start":55769141,"end":55773179,"strand":1,"description":"ret finger protein like 4A like 1 [Source:HGNC Symbol;Acc:HGNC:45147]"}, {"versioned_ensembl_gene_id":"ENSG00000271404.1","gene_symbol":"MZT1P2","gene_name":"mitotic spindle organizing protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50606]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929581","summary":null,"start":139228221,"end":139228605,"strand":1,"description":"mitotic spindle organizing protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50606]"}, {"versioned_ensembl_gene_id":"ENSG00000081041.8","gene_symbol":"CXCL2","gene_name":"C-X-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:4603]","synonyms":"SCYB2,MIP-2a,MGSA-b,GROb,GRO2,CINC-2a","biotype":"protein_coding","ncbi_id":"2920","summary":"This antimicrobial gene is part of a chemokine superfamily that encodes secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CXC subfamily, is expressed at sites of inflammation and may suppress hematopoietic progenitor cell proliferation. [provided by RefSeq, Sep 2014]","start":74097035,"end":74099293,"strand":-1,"description":"C-X-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:4603]"}, {"versioned_ensembl_gene_id":"ENSG00000241129.3","gene_symbol":"AC093719.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":124935455,"end":124935895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170948.3","gene_symbol":"MBD3L1","gene_name":"methyl-CpG binding domain protein 3 like 1 [Source:HGNC Symbol;Acc:HGNC:15774]","synonyms":"MBD3L","biotype":"protein_coding","ncbi_id":"85509","summary":"This gene encodes a protein that is related to methyl-CpG-binding proteins but lacks the methyl-CpG binding domain. The protein is localized to discrete areas in the nucleus, and expression appears to be restricted to round spermatids, suggesting that the protein plays a role in the postmeiotic stages of male germ cell development. [provided by RefSeq, Jul 2008]","start":8832398,"end":8843340,"strand":1,"description":"methyl-CpG binding domain protein 3 like 1 [Source:HGNC Symbol;Acc:HGNC:15774]"}, {"versioned_ensembl_gene_id":"ENSG00000233005.1","gene_symbol":"AC018742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21221175,"end":21970959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176378.8","gene_symbol":"PFN1P10","gene_name":"profilin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42985]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"767853","summary":null,"start":21459756,"end":21460082,"strand":-1,"description":"profilin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42985]"}, {"versioned_ensembl_gene_id":"ENSG00000261511.1","gene_symbol":"CYP3A137P","gene_name":"cytochrome P450 family 3 subfamily A member 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:42419]","synonyms":"CYP3A43-de1b","biotype":"unprocessed_pseudogene","ncbi_id":"107063543","summary":null,"start":99820018,"end":99820086,"strand":1,"description":"cytochrome P450 family 3 subfamily A member 137, pseudogene [Source:HGNC Symbol;Acc:HGNC:42419]"}, {"versioned_ensembl_gene_id":"ENSG00000122417.15","gene_symbol":"ODF2L","gene_name":"outer dense fiber of sperm tails 2 like [Source:HGNC Symbol;Acc:HGNC:29225]","synonyms":"KIAA1229","biotype":"protein_coding","ncbi_id":"57489","summary":null,"start":86346824,"end":86396342,"strand":-1,"description":"outer dense fiber of sperm tails 2 like [Source:HGNC Symbol;Acc:HGNC:29225]"}, {"versioned_ensembl_gene_id":"ENSG00000121570.12","gene_symbol":"DPPA4","gene_name":"developmental pluripotency associated 4 [Source:HGNC Symbol;Acc:HGNC:19200]","synonyms":"FLJ10713","biotype":"protein_coding","ncbi_id":"55211","summary":"This gene encodes a nuclear factor that is involved in the maintenance of pluripotency in stem cells and essential for embryogenesis. The encoded protein has a scaffold-attachment factor A/B, acinus and PIAS (SAP) domain that binds DNA and is thought to modify chromatin. Mice with a homozygous knockout of the orthologous gene die during late embryonic development or within hours after birth. Knockout embryos are normal in size at embryonic day 18.5 but exhibit skeletal and lung tissue abnormalities. This gene, when mutated, is highly expressed in embryonal carcinomas, pluripotent germ cell tumors, and other cancers and is thought to play an important role in tumor progression. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":109326141,"end":109337572,"strand":-1,"description":"developmental pluripotency associated 4 [Source:HGNC Symbol;Acc:HGNC:19200]"}, {"versioned_ensembl_gene_id":"ENSG00000281131.1","gene_symbol":"SCHLAP1","gene_name":"SWI/SNF complex antagonist associated with prostate cancer 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48603]","synonyms":"SChLAP1,PCAT11,LINC00913","biotype":"lincRNA","ncbi_id":"101669767","summary":null,"start":180692104,"end":180916939,"strand":1,"description":"SWI/SNF complex antagonist associated with prostate cancer 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48603]"}, {"versioned_ensembl_gene_id":"ENSG00000279559.1","gene_symbol":"AC104820.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":180801227,"end":180801533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225258.1","gene_symbol":"AC009478.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180571712,"end":180692454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271672.1","gene_symbol":"DUXAP8","gene_name":"double homeobox A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:32187]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"503637","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":15826566,"end":15827187,"strand":1,"description":"double homeobox A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:32187]"}, {"versioned_ensembl_gene_id":"ENSG00000279537.1","gene_symbol":"AC020658.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":40244925,"end":40247366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264707.1","gene_symbol":"L3MBTL4-AS1","gene_name":"L3MBTL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51320]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927150","summary":null,"start":6256747,"end":6260934,"strand":1,"description":"L3MBTL4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51320]"}, {"versioned_ensembl_gene_id":"ENSG00000272872.1","gene_symbol":"AP000525.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":15823197,"end":15823890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231564.1","gene_symbol":"EIF4A1P11","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130006","summary":null,"start":179201705,"end":179201926,"strand":1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37932]"}, {"versioned_ensembl_gene_id":"ENSG00000203897.3","gene_symbol":"SPATA42","gene_name":"spermatogenesis associated 42 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:41198]","synonyms":"SRG7,AKNAD1-AS1","biotype":"antisense_RNA","ncbi_id":"642864","summary":null,"start":108857217,"end":108858524,"strand":1,"description":"spermatogenesis associated 42 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:41198]"}, {"versioned_ensembl_gene_id":"ENSG00000253319.1","gene_symbol":"AC134698.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43511820,"end":43512033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145293.15","gene_symbol":"ENOPH1","gene_name":"enolase-phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:24599]","synonyms":"mtnC,MASA,E1","biotype":"protein_coding","ncbi_id":"58478","summary":null,"start":82430562,"end":82461091,"strand":1,"description":"enolase-phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:24599]"}, {"versioned_ensembl_gene_id":"ENSG00000272135.5","gene_symbol":"AL359747.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":122818816,"end":122826449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230335.1","gene_symbol":"DNAJB5P1","gene_name":"DnaJ heat shock protein family (Hsp40) member B5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50449]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76931261,"end":76932066,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50449]"}, {"versioned_ensembl_gene_id":"ENSG00000234828.8","gene_symbol":"IQCM","gene_name":"IQ motif containing M [Source:HGNC Symbol;Acc:HGNC:53443]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285423","summary":null,"start":149351903,"end":149896233,"strand":-1,"description":"IQ motif containing M [Source:HGNC Symbol;Acc:HGNC:53443]"}, {"versioned_ensembl_gene_id":"ENSG00000084674.14","gene_symbol":"APOB","gene_name":"apolipoprotein B [Source:HGNC Symbol;Acc:HGNC:603]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338","summary":"This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins (LDL), and is the ligand for the LDL receptor. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. [provided by RefSeq, Dec 2019]","start":21001429,"end":21044073,"strand":-1,"description":"apolipoprotein B [Source:HGNC Symbol;Acc:HGNC:603]"}, {"versioned_ensembl_gene_id":"ENSG00000226064.1","gene_symbol":"PGBD4P6","gene_name":"piggyBac transposable element derived 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44071]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421180","summary":null,"start":143343976,"end":143344585,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44071]"}, {"versioned_ensembl_gene_id":"ENSG00000138642.14","gene_symbol":"HERC6","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase family member 6 [Source:HGNC Symbol;Acc:HGNC:26072]","synonyms":"FLJ20637","biotype":"protein_coding","ncbi_id":"55008","summary":"HERC6 belongs to the HERC family of ubiquitin ligases, all of which contain a HECT domain and at least 1 RCC1 (MIM 179710)-like domain (RLD). The 350-amino acid HECT domain is predicted to catalyze the formation of a thioester with ubiquitin before transferring it to a substrate, and the RLD is predicted to act as a guanine nucleotide exchange factor for small G proteins (Hochrainer et al., 2005 [PubMed 15676274]).[supplied by OMIM, Mar 2008]","start":88378739,"end":88443111,"strand":1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase family member 6 [Source:HGNC Symbol;Acc:HGNC:26072]"}, {"versioned_ensembl_gene_id":"ENSG00000236576.1","gene_symbol":"AC241520.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51856968,"end":51858066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280666.1","gene_symbol":"AC106772.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":524705,"end":526594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241838.3","gene_symbol":"AP000529.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15721486,"end":15722608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006837.11","gene_symbol":"CDKL3","gene_name":"cyclin dependent kinase like 3 [Source:HGNC Symbol;Acc:HGNC:15483]","synonyms":"NKIAMRE","biotype":"protein_coding","ncbi_id":"51265","summary":"The protein encoded by this gene is a member of cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of Saccharomyces cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, and are known to be important regulators of cell cycle progression. This gene was identified as a gene absent in leukemic patients with chromosome 5q deletion. This loss may be an important determinant of dysmyelopoiesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":134286350,"end":134371047,"strand":-1,"description":"cyclin dependent kinase like 3 [Source:HGNC Symbol;Acc:HGNC:15483]"}, {"versioned_ensembl_gene_id":"ENSG00000221844.2","gene_symbol":"DPP3P2","gene_name":"dipeptidyl peptidase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"138971","summary":null,"start":73474378,"end":73476073,"strand":-1,"description":"dipeptidyl peptidase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51350]"}, {"versioned_ensembl_gene_id":"ENSG00000236756.4","gene_symbol":"DNAJC9-AS1","gene_name":"DNAJC9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31432]","synonyms":"bA537A6.3,C10orf103,bA537A6.3,C10orf103","biotype":"antisense_RNA","ncbi_id":"414245","summary":null,"start":73247360,"end":73276984,"strand":1,"description":"DNAJC9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31432]"}, {"versioned_ensembl_gene_id":"ENSG00000267644.1","gene_symbol":"AC061975.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28219285,"end":28220005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225745.8","gene_symbol":"AL773572.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41176322,"end":41186788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227001.3","gene_symbol":"NBPF2P","gene_name":"NBPF member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:31987]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"343381","summary":"This pseudogene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2013]","start":21424625,"end":21427967,"strand":-1,"description":"NBPF member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:31987]"}, {"versioned_ensembl_gene_id":"ENSG00000237891.1","gene_symbol":"AL441985.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122010976,"end":122011612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234701.1","gene_symbol":"PRDX3P3","gene_name":"peroxiredoxin 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39266]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128902","summary":null,"start":38617419,"end":38617940,"strand":-1,"description":"peroxiredoxin 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39266]"}, {"versioned_ensembl_gene_id":"ENSG00000171044.10","gene_symbol":"XKR6","gene_name":"XK related 6 [Source:HGNC Symbol;Acc:HGNC:27806]","synonyms":"C8orf7,C8orf5,C8orf21","biotype":"protein_coding","ncbi_id":"286046","summary":null,"start":10896045,"end":11201366,"strand":-1,"description":"XK related 6 [Source:HGNC Symbol;Acc:HGNC:27806]"}, {"versioned_ensembl_gene_id":"ENSG00000268480.1","gene_symbol":"LINC01862","gene_name":"long intergenic non-protein coding RNA 1862 [Source:HGNC Symbol;Acc:HGNC:52681]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372267","summary":null,"start":8630671,"end":8638649,"strand":1,"description":"long intergenic non-protein coding RNA 1862 [Source:HGNC Symbol;Acc:HGNC:52681]"}, {"versioned_ensembl_gene_id":"ENSG00000280688.1","gene_symbol":"CEP72","gene_name":"centrosomal protein 72 [Source:HGNC Symbol;Acc:HGNC:25547]","synonyms":"KIAA1519,FLJ10565","biotype":"protein_coding","ncbi_id":"55722","summary":"The product of this gene is a member of the leucine-rich-repeat (LRR) superfamily of proteins. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. [provided by RefSeq, Jul 2008]","start":614020,"end":626253,"strand":1,"description":"centrosomal protein 72 [Source:HGNC Symbol;Acc:HGNC:25547]"}, {"versioned_ensembl_gene_id":"ENSG00000109680.10","gene_symbol":"TBC1D19","gene_name":"TBC1 domain family member 19 [Source:HGNC Symbol;Acc:HGNC:25624]","synonyms":"FLJ11082","biotype":"protein_coding","ncbi_id":"55296","summary":null,"start":26576437,"end":26755351,"strand":1,"description":"TBC1 domain family member 19 [Source:HGNC Symbol;Acc:HGNC:25624]"}, {"versioned_ensembl_gene_id":"ENSG00000237881.6","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32392894,"end":32448091,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000253195.2","gene_symbol":"AC134698.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43542076,"end":43544057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108061.11","gene_symbol":"SHOC2","gene_name":"SHOC2, leucine rich repeat scaffold protein [Source:HGNC Symbol;Acc:HGNC:15454]","synonyms":"SUR8,SUR-8,SOC2,SOC-2,KIAA0862","biotype":"protein_coding","ncbi_id":"8036","summary":"This gene encodes a protein that consists almost entirely of leucine-rich repeats, a domain implicated in protein-protein interactions. The protein may function as a scaffold linking RAS to downstream signal transducers in the RAS/ERK MAP kinase signaling cascade. Mutations in this gene have been associated with Noonan-like syndrome with loose anagen hair. [provided by RefSeq, May 2010]","start":110919547,"end":111013667,"strand":1,"description":"SHOC2, leucine rich repeat scaffold protein [Source:HGNC Symbol;Acc:HGNC:15454]"}, {"versioned_ensembl_gene_id":"ENSG00000249175.1","gene_symbol":"AC008534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94788789,"end":94793599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260115.1","gene_symbol":"AC012174.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61918321,"end":61940697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262554.1","gene_symbol":"AC004232.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":3308609,"end":3308816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232381.1","gene_symbol":"OR52U1P","gene_name":"olfactory receptor family 52 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15237]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"81243","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5719290,"end":5720212,"strand":1,"description":"olfactory receptor family 52 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15237]"}, {"versioned_ensembl_gene_id":"ENSG00000154358.20","gene_symbol":"OBSCN","gene_name":"obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [Source:HGNC Symbol;Acc:HGNC:15719]","synonyms":"UNC89,KIAA1639,KIAA1556,ARHGEF30","biotype":"protein_coding","ncbi_id":"84033","summary":"The obscurin gene spans more than 150 kb, contains over 80 exons and encodes a protein of approximately 720 kDa. The encoded protein contains 68 Ig domains, 2 fibronectin domains, 1 calcium/calmodulin-binding domain, 1 RhoGEF domain with an associated PH domain, and 2 serine-threonine kinase domains. This protein belongs to the family of giant sacromeric signaling proteins that includes titin and nebulin, and may have a role in the organization of myofibrils during assembly and may mediate interactions between the sarcoplasmic reticulum and myofibrils. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":228208130,"end":228378874,"strand":1,"description":"obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [Source:HGNC Symbol;Acc:HGNC:15719]"}, {"versioned_ensembl_gene_id":"ENSG00000158639.12","gene_symbol":"PAGE5","gene_name":"PAGE family member 5 [Source:HGNC Symbol;Acc:HGNC:29992]","synonyms":"PAGE-5,CT16.2,CT16.1","biotype":"protein_coding","ncbi_id":"90737","summary":"This gene is a member of family of proteins that are expressed in a variety of tumors and in some fetal and reproductive tissues. The encoded protein may protect cells from programmed cell death. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jan 2015]","start":55220355,"end":55224108,"strand":1,"description":"PAGE family member 5 [Source:HGNC Symbol;Acc:HGNC:29992]"}, {"versioned_ensembl_gene_id":"ENSG00000281005.1","gene_symbol":"LINC00921","gene_name":"long intergenic non-protein coding RNA 921 [Source:HGNC Symbol;Acc:HGNC:26830]","synonyms":"FLJ39639","biotype":"lincRNA","ncbi_id":"283876","summary":null,"start":3263743,"end":3267567,"strand":1,"description":"long intergenic non-protein coding RNA 921 [Source:HGNC Symbol;Acc:HGNC:26830]"}, {"versioned_ensembl_gene_id":"ENSG00000118961.14","gene_symbol":"LDAH","gene_name":"lipid droplet associated hydrolase [Source:HGNC Symbol;Acc:HGNC:26145]","synonyms":"C2orf43,FLJ21820","biotype":"protein_coding","ncbi_id":"60526","summary":null,"start":20684014,"end":20823130,"strand":-1,"description":"lipid droplet associated hydrolase [Source:HGNC Symbol;Acc:HGNC:26145]"}, {"versioned_ensembl_gene_id":"ENSG00000187595.15","gene_symbol":"ZNF385C","gene_name":"zinc finger protein 385C [Source:HGNC Symbol;Acc:HGNC:33722]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201181","summary":null,"start":42025576,"end":42098479,"strand":-1,"description":"zinc finger protein 385C [Source:HGNC Symbol;Acc:HGNC:33722]"}, {"versioned_ensembl_gene_id":"ENSG00000229665.8","gene_symbol":"PRR20C","gene_name":"proline rich 20C [Source:HGNC Symbol;Acc:HGNC:37221]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729240","summary":"This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008]","start":57140918,"end":57157082,"strand":1,"description":"proline rich 20C [Source:HGNC Symbol;Acc:HGNC:37221]"}, {"versioned_ensembl_gene_id":"ENSG00000236094.1","gene_symbol":"LINC00545","gene_name":"long intergenic non-protein coding RNA 545 [Source:HGNC Symbol;Acc:HGNC:43680]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440132","summary":null,"start":30882551,"end":30883395,"strand":1,"description":"long intergenic non-protein coding RNA 545 [Source:HGNC Symbol;Acc:HGNC:43680]"}, {"versioned_ensembl_gene_id":"ENSG00000275244.1","gene_symbol":"OR2T1","gene_name":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]","synonyms":"OR1-25","biotype":"protein_coding","ncbi_id":"26696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248412061,"end":248413170,"strand":1,"description":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]"}, {"versioned_ensembl_gene_id":"ENSG00000249051.2","gene_symbol":"AC112518.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73777636,"end":73778060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170743.16","gene_symbol":"SYT9","gene_name":"synaptotagmin 9 [Source:HGNC Symbol;Acc:HGNC:19265]","synonyms":null,"biotype":"protein_coding","ncbi_id":"143425","summary":null,"start":7238778,"end":7469042,"strand":1,"description":"synaptotagmin 9 [Source:HGNC Symbol;Acc:HGNC:19265]"}, {"versioned_ensembl_gene_id":"ENSG00000277715.1","gene_symbol":"AC079174.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106250759,"end":106252786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102802.9","gene_symbol":"MEDAG","gene_name":"mesenteric estrogen dependent adipogenesis [Source:HGNC Symbol;Acc:HGNC:25926]","synonyms":"MEDA-4,FLJ14834,C13orf33,AWMS3","biotype":"protein_coding","ncbi_id":"84935","summary":null,"start":30906191,"end":30925572,"strand":1,"description":"mesenteric estrogen dependent adipogenesis [Source:HGNC Symbol;Acc:HGNC:25926]"}, {"versioned_ensembl_gene_id":"ENSG00000239924.1","gene_symbol":"RPL29P22","gene_name":"ribosomal protein L29 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35675]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271472","summary":null,"start":63115880,"end":63116338,"strand":-1,"description":"ribosomal protein L29 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35675]"}, {"versioned_ensembl_gene_id":"ENSG00000121966.6","gene_symbol":"CXCR4","gene_name":"C-X-C motif chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:2561]","synonyms":"NPY3R,LESTR,HSY3RR,HM89,fusin,D2S201E,CD184,NPYY3R,NPYR","biotype":"protein_coding","ncbi_id":"7852","summary":"This gene encodes a CXC chemokine receptor specific for stromal cell-derived factor-1. The protein has 7 transmembrane regions and is located on the cell surface. It acts with the CD4 protein to support HIV entry into cells and is also highly expressed in breast cancer cells. Mutations in this gene have been associated with WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":136114349,"end":136118165,"strand":-1,"description":"C-X-C motif chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:2561]"}, {"versioned_ensembl_gene_id":"ENSG00000243970.1","gene_symbol":"PPIEL","gene_name":"peptidylprolyl isomerase E like pseudogene [Source:HGNC Symbol;Acc:HGNC:33195]","synonyms":"PPIEP1","biotype":"unprocessed_pseudogene","ncbi_id":"728448","summary":"This transcribed pseudogene is related to PPIE (Gene ID: 10450). Expression of this pseudogene may be downregulated in non-small cell lung cancer (NSCLC). Differential DNA methylation of this locus may be associated with intellectual disability and bipolar disorder in human patients. [provided by RefSeq, Sep 2016]","start":39531838,"end":39558707,"strand":-1,"description":"peptidylprolyl isomerase E like pseudogene [Source:HGNC Symbol;Acc:HGNC:33195]"}, {"versioned_ensembl_gene_id":"ENSG00000256181.1","gene_symbol":"AP001880.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63265836,"end":63266256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274090.1","gene_symbol":"AL354821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55535697,"end":55583524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235934.1","gene_symbol":"AC007405.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170816293,"end":170818037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223467.2","gene_symbol":"CALM1P1","gene_name":"calmodulin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1443]","synonyms":"CALML1","biotype":"processed_pseudogene","ncbi_id":"802","summary":null,"start":95499604,"end":95500036,"strand":1,"description":"calmodulin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1443]"}, {"versioned_ensembl_gene_id":"ENSG00000204478.9","gene_symbol":"PRAMEF20","gene_name":"PRAME family member 20 [Source:HGNC Symbol;Acc:HGNC:25224]","synonyms":"PRAMEF21,OTTHUMT00000008157,OTTHUMG00000007911","biotype":"protein_coding","ncbi_id":"645425","summary":null,"start":13410450,"end":13421328,"strand":1,"description":"PRAME family member 20 [Source:HGNC Symbol;Acc:HGNC:25224]"}, {"versioned_ensembl_gene_id":"ENSG00000275700.4","gene_symbol":"AATF","gene_name":"apoptosis antagonizing transcription factor [Source:HGNC Symbol;Acc:HGNC:19235]","synonyms":"BFR2,DED,CHE1,CHE-1","biotype":"protein_coding","ncbi_id":"26574","summary":"The protein encoded by this gene was identified on the basis of its interaction with MAP3K12/DLK, a protein kinase known to be involved in the induction of cell apoptosis. This gene product contains a leucine zipper, which is a characteristic motif of transcription factors, and was shown to exhibit strong transactivation activity when fused to Gal4 DNA binding domain. Overexpression of this gene interfered with MAP3K12 induced apoptosis. [provided by RefSeq, Jul 2008]","start":36948875,"end":37056871,"strand":1,"description":"apoptosis antagonizing transcription factor [Source:HGNC Symbol;Acc:HGNC:19235]"}, {"versioned_ensembl_gene_id":"ENSG00000277911.1","gene_symbol":"AC243773.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36980167,"end":36980422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229903.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32429909,"end":32433086,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000106484.14","gene_symbol":"MEST","gene_name":"mesoderm specific transcript [Source:HGNC Symbol;Acc:HGNC:7028]","synonyms":"PEG1","biotype":"protein_coding","ncbi_id":"4232","summary":"This gene encodes a member of the alpha/beta hydrolase superfamily. It is imprinted, exhibiting preferential expression from the paternal allele in fetal tissues, and isoform-specific imprinting in lymphocytes. The loss of imprinting of this gene has been linked to certain types of cancer and may be due to promotor switching. The encoded protein may play a role in development. Alternatively spliced transcript variants encoding multiple isoforms have been identified for this gene. Pseudogenes of this gene are located on the short arm of chromosomes 3 and 4, and the long arm of chromosomes 6 and 15. [provided by RefSeq, Dec 2011]","start":130486171,"end":130506296,"strand":1,"description":"mesoderm specific transcript [Source:HGNC Symbol;Acc:HGNC:7028]"}, {"versioned_ensembl_gene_id":"ENSG00000213152.5","gene_symbol":"AC004217.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112301870,"end":112302663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282796.1","gene_symbol":"IGHV1-14","gene_name":"immunoglobulin heavy variable 1-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5547]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28470","summary":null,"start":106146662,"end":106146902,"strand":-1,"description":"immunoglobulin heavy variable 1-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5547]"}, {"versioned_ensembl_gene_id":"ENSG00000214020.3","gene_symbol":"FTLP4","gene_name":"ferritin light chain pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37952]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129251","summary":null,"start":30935485,"end":30935977,"strand":1,"description":"ferritin light chain pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37952]"}, {"versioned_ensembl_gene_id":"ENSG00000261739.2","gene_symbol":"GOLGA8S","gene_name":"golgin A8 family member S [Source:HGNC Symbol;Acc:HGNC:44409]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653061","summary":null,"start":23354748,"end":23367231,"strand":1,"description":"golgin A8 family member S [Source:HGNC Symbol;Acc:HGNC:44409]"}, {"versioned_ensembl_gene_id":"ENSG00000240874.1","gene_symbol":"AC025271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57555951,"end":57556379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276772.1","gene_symbol":"AC025271.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57553955,"end":57555680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258985.1","gene_symbol":"AL352979.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53036755,"end":53038251,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227698.1","gene_symbol":"AP001619.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41874756,"end":41877613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004059.10","gene_symbol":"ARF5","gene_name":"ADP ribosylation factor 5 [Source:HGNC Symbol;Acc:HGNC:658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"381","summary":"This gene is a member of the human ADP-ribosylation factor (ARF) gene family. These genes encode small guanine nucleotide-binding proteins that stimulate the ADP-ribosyltransferase activity of cholera toxin and play a role in vesicular trafficking and as activators of phospholipase D. The gene products include 6 ARF proteins and 11 ARF-like proteins and constitute 1 family of the RAS superfamily. The ARF proteins are categorized as class I (ARF1, ARF2,and ARF3), class II (ARF4 and ARF5) and class III (ARF6). The members of each class share a common gene organization. [provided by RefSeq, Dec 2010]","start":127588345,"end":127591705,"strand":1,"description":"ADP ribosylation factor 5 [Source:HGNC Symbol;Acc:HGNC:658]"}, {"versioned_ensembl_gene_id":"ENSG00000264260.1","gene_symbol":"LINC01893","gene_name":"long intergenic non-protein coding RNA 1893 [Source:HGNC Symbol;Acc:HGNC:52712]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372207","summary":null,"start":76209510,"end":76215702,"strand":1,"description":"long intergenic non-protein coding RNA 1893 [Source:HGNC Symbol;Acc:HGNC:52712]"}, {"versioned_ensembl_gene_id":"ENSG00000226582.1","gene_symbol":"UBE2V1P5","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287173","summary":null,"start":114117147,"end":114117551,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44888]"}, {"versioned_ensembl_gene_id":"ENSG00000258478.1","gene_symbol":"AC009396.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78744398,"end":78753878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258637.1","gene_symbol":"AC008056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79661666,"end":79791263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239438.1","gene_symbol":"RPS26P48","gene_name":"ribosomal protein S26 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:35519]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271574","summary":null,"start":78231281,"end":78231619,"strand":-1,"description":"ribosomal protein S26 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:35519]"}, {"versioned_ensembl_gene_id":"ENSG00000175104.14","gene_symbol":"TRAF6","gene_name":"TNF receptor associated factor 6 [Source:HGNC Symbol;Acc:HGNC:12036]","synonyms":"RNF85","biotype":"protein_coding","ncbi_id":"7189","summary":"The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins are associated with, and mediate signal transduction from, members of the TNF receptor superfamily. This protein mediates signaling from members of the TNF receptor superfamily as well as the Toll/IL-1 family. Signals from receptors such as CD40, TNFSF11/RANCE and IL-1 have been shown to be mediated by this protein. This protein also interacts with various protein kinases including IRAK1/IRAK, SRC and PKCzeta, which provides a link between distinct signaling pathways. This protein functions as a signal transducer in the NF-kappaB pathway that activates IkappaB kinase (IKK) in response to proinflammatory cytokines. The interaction of this protein with UBE2N/UBC13, and UBE2V1/UEV1A, which are ubiquitin conjugating enzymes catalyzing the formation of polyubiquitin chains, has been found to be required for IKK activation by this protein. This protein also interacts with the transforming growth factor (TGF) beta receptor complex and is required for Smad-independent activation of the JNK and p38 kinases. This protein has an amino terminal RING domain which is followed by four zinc-finger motifs, a central coiled-coil region and a highly conserved carboxyl terminal domain, known as the TRAF-C domain. Two alternatively spliced transcript variants, encoding an identical protein, have been reported. [provided by RefSeq, Feb 2012]","start":36487027,"end":36510272,"strand":-1,"description":"TNF receptor associated factor 6 [Source:HGNC Symbol;Acc:HGNC:12036]"}, {"versioned_ensembl_gene_id":"ENSG00000154645.13","gene_symbol":"CHODL","gene_name":"chondrolectin [Source:HGNC Symbol;Acc:HGNC:17807]","synonyms":"PRED12,MT75,FLJ12627,C21orf68","biotype":"protein_coding","ncbi_id":"140578","summary":"This gene encodes a type I membrane protein with a carbohydrate recognition domain characteristic of C-type lectins in its extracellular portion. In other proteins, this domain is involved in endocytosis of glycoproteins and exogenous sugar-bearing pathogens. This protein localizes predominantly to the perinuclear region. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":17901263,"end":18267373,"strand":1,"description":"chondrolectin [Source:HGNC Symbol;Acc:HGNC:17807]"}, {"versioned_ensembl_gene_id":"ENSG00000259106.1","gene_symbol":"AC008056.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79611418,"end":79633311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224853.1","gene_symbol":"LINC00393","gene_name":"long intergenic non-protein coding RNA 393 [Source:HGNC Symbol;Acc:HGNC:42721]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874156","summary":null,"start":73413473,"end":73648253,"strand":-1,"description":"long intergenic non-protein coding RNA 393 [Source:HGNC Symbol;Acc:HGNC:42721]"}, {"versioned_ensembl_gene_id":"ENSG00000227330.1","gene_symbol":"AF130417.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18022370,"end":18114904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225235.1","gene_symbol":"INTS6L-AS1","gene_name":"INTS6L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41180]","synonyms":"DDX26B-AS1","biotype":"antisense_RNA","ncbi_id":"100874118","summary":null,"start":135520083,"end":135520674,"strand":-1,"description":"INTS6L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41180]"}, {"versioned_ensembl_gene_id":"ENSG00000224399.11","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"D6S2244E,ZIP7,HKE4,RING5,H2-KE4,KE4","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33370805,"end":33374799,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000152377.13","gene_symbol":"SPOCK1","gene_name":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 1 [Source:HGNC Symbol;Acc:HGNC:11251]","synonyms":"TIC1,testican-1,SPOCK","biotype":"protein_coding","ncbi_id":"6695","summary":"This gene encodes the protein core of a seminal plasma proteoglycan containing chondroitin- and heparan-sulfate chains. The protein's function is unknown, although similarity to thyropin-type cysteine protease-inhibitors suggests its function may be related to protease inhibition. [provided by RefSeq, Jul 2008]","start":136975298,"end":137598379,"strand":-1,"description":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 1 [Source:HGNC Symbol;Acc:HGNC:11251]"}, {"versioned_ensembl_gene_id":"ENSG00000054690.13","gene_symbol":"PLEKHH1","gene_name":"pleckstrin homology, MyTH4 and FERM domain containing H1 [Source:HGNC Symbol;Acc:HGNC:17733]","synonyms":"KIAA1200","biotype":"protein_coding","ncbi_id":"57475","summary":null,"start":67533301,"end":67589612,"strand":1,"description":"pleckstrin homology, MyTH4 and FERM domain containing H1 [Source:HGNC Symbol;Acc:HGNC:17733]"}, {"versioned_ensembl_gene_id":"ENSG00000267905.5","gene_symbol":"AC008750.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51340695,"end":51344117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197180.2","gene_symbol":"CH17-340M24.3","gene_name":"uncharacterized protein BC009467 [Source:NCBI gene;Acc:158960]","synonyms":null,"biotype":"lincRNA","ncbi_id":"158960","summary":null,"start":154424380,"end":154428479,"strand":-1,"description":"uncharacterized protein BC009467 [Source:NCBI gene;Acc:158960]"}, {"versioned_ensembl_gene_id":"ENSG00000229342.3","gene_symbol":"MYL8P","gene_name":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]","synonyms":"BING3","biotype":"processed_pseudogene","ncbi_id":"442204","summary":null,"start":33316901,"end":33317418,"strand":1,"description":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]"}, {"versioned_ensembl_gene_id":"ENSG00000280194.1","gene_symbol":"AD000864.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35901561,"end":35903855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173275.12","gene_symbol":"ZNF449","gene_name":"zinc finger protein 449 [Source:HGNC Symbol;Acc:HGNC:21039]","synonyms":"ZSCAN19,FLJ23614","biotype":"protein_coding","ncbi_id":"203523","summary":"This gene encodes a nuclear protein that likely functions as a transcription factor. The protein includes an N-terminal SCAN domain, and seven C2H2-type zinc finger motifs. [provided by RefSeq, May 2010]","start":135344796,"end":135363152,"strand":1,"description":"zinc finger protein 449 [Source:HGNC Symbol;Acc:HGNC:21039]"}, {"versioned_ensembl_gene_id":"ENSG00000282416.1","gene_symbol":"AC092299.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197310,"end":198066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226055.2","gene_symbol":"PAICSP1","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8588]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780814","summary":null,"start":37878116,"end":37879493,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8588]"}, {"versioned_ensembl_gene_id":"ENSG00000254843.1","gene_symbol":"XIAPP2","gene_name":"X-linked inhibitor of apoptosis pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420509","summary":null,"start":87094734,"end":87096585,"strand":-1,"description":"X-linked inhibitor of apoptosis pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52376]"}, {"versioned_ensembl_gene_id":"ENSG00000274751.1","gene_symbol":"AC120498.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1305547,"end":1309413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236211.1","gene_symbol":"MTCO1P7","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52009]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075263","summary":null,"start":130273908,"end":130275449,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:52009]"}, {"versioned_ensembl_gene_id":"ENSG00000275827.1","gene_symbol":"AC021506.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75927836,"end":75928004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268758.7","gene_symbol":"ADGRE4P","gene_name":"adhesion G protein-coupled receptor E4, pseudogene [Source:HGNC Symbol;Acc:HGNC:19240]","synonyms":"GPR127,EMR4P,EMR4,PGR16","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"326342","summary":"This gene is a member of the EGF-TM7 receptor gene family which is thought to play a role in leukocyte adhesion and migration. In other vertebrates, including nonhuman primates, this gene encodes a protein containing N-terminal EGF domains and a C-terminal transmembrane domain. Sequence evidence for the human gene, however, indicates nucleotide deletion in the genomic sequence would result in frameshift and early termination of translation. A protein expressed by this gene would be soluble rather than expressed on the cell surface. As the encoded protein has not been detected, this gene may represent a transcribed pseudogene. [provided by RefSeq, Aug 2008]","start":6952500,"end":6997872,"strand":-1,"description":"adhesion G protein-coupled receptor E4, pseudogene [Source:HGNC Symbol;Acc:HGNC:19240]"}, {"versioned_ensembl_gene_id":"ENSG00000279982.1","gene_symbol":"AL162274.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131996738,"end":131999846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267745.1","gene_symbol":"AC060766.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":35406684,"end":35409768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198162.12","gene_symbol":"MAN1A2","gene_name":"mannosidase alpha class 1A member 2 [Source:HGNC Symbol;Acc:HGNC:6822]","synonyms":"MAN1B","biotype":"protein_coding","ncbi_id":"10905","summary":"Alpha-mannosidases function at different stages of N-glycan maturation in mammalian cells. See MAN2A1 (MIM 154582) for general information.[supplied by OMIM, Mar 2008]","start":117367449,"end":117528872,"strand":1,"description":"mannosidase alpha class 1A member 2 [Source:HGNC Symbol;Acc:HGNC:6822]"}, {"versioned_ensembl_gene_id":"ENSG00000196865.4","gene_symbol":"NHLRC2","gene_name":"NHL repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:24731]","synonyms":"FLJ25621,FLJ20147,DKFZp779F115,MGC45492,FLJ33312","biotype":"protein_coding","ncbi_id":"374354","summary":null,"start":113854661,"end":113917194,"strand":1,"description":"NHL repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:24731]"}, {"versioned_ensembl_gene_id":"ENSG00000130813.17","gene_symbol":"C19orf66","gene_name":"chromosome 19 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:25649]","synonyms":"RyDEN,IRAV,FLJ11286","biotype":"protein_coding","ncbi_id":"55337","summary":null,"start":10086122,"end":10093252,"strand":1,"description":"chromosome 19 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:25649]"}, {"versioned_ensembl_gene_id":"ENSG00000236105.1","gene_symbol":"PRELID3BP10","gene_name":"PRELI domain containing 3B pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646873","summary":null,"start":127295620,"end":127296203,"strand":1,"description":"PRELI domain containing 3B pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49072]"}, {"versioned_ensembl_gene_id":"ENSG00000132436.11","gene_symbol":"FIGNL1","gene_name":"fidgetin like 1 [Source:HGNC Symbol;Acc:HGNC:13286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63979","summary":"This gene encodes a member of the AAA ATPase family of proteins. The encoded protein is recruited to sites of DNA damage where it plays a role in DNA double-strand break repair via homologous recombination. This protein has also been shown to localize to the centrosome and inhibit ciliogenesis, and may regulate the proliferation and differentiation of osteoblasts. [provided by RefSeq, Oct 2016]","start":50444128,"end":50542535,"strand":-1,"description":"fidgetin like 1 [Source:HGNC Symbol;Acc:HGNC:13286]"}, {"versioned_ensembl_gene_id":"ENSG00000277751.4","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"LIR-2,MIR10,ILT4,MIR-10,CD85d,LIR2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54274438,"end":54278995,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000162946.21","gene_symbol":"DISC1","gene_name":"disrupted in schizophrenia 1 [Source:HGNC Symbol;Acc:HGNC:2888]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27185","summary":"This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1;11)(q42.1;q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":231626815,"end":232041272,"strand":1,"description":"disrupted in schizophrenia 1 [Source:HGNC Symbol;Acc:HGNC:2888]"}, {"versioned_ensembl_gene_id":"ENSG00000008283.15","gene_symbol":"CYB561","gene_name":"cytochrome b561 [Source:HGNC Symbol;Acc:HGNC:2571]","synonyms":"FRRS2,CYB561A1","biotype":"protein_coding","ncbi_id":"1534","summary":null,"start":63432304,"end":63446378,"strand":-1,"description":"cytochrome b561 [Source:HGNC Symbol;Acc:HGNC:2571]"}, {"versioned_ensembl_gene_id":"ENSG00000109625.18","gene_symbol":"CPZ","gene_name":"carboxypeptidase Z [Source:HGNC Symbol;Acc:HGNC:2333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8532","summary":"This gene encodes a member of the metallocarboxypeptidase family. This enzyme displays carboxypeptidase activity towards substrates with basic C-terminal residues. It is most active at neutral pH and is inhibited by active site-directed inhibitors of metallocarboxypeptidases. Alternative splicing in the coding region results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":8592660,"end":8619759,"strand":1,"description":"carboxypeptidase Z [Source:HGNC Symbol;Acc:HGNC:2333]"}, {"versioned_ensembl_gene_id":"ENSG00000255548.1","gene_symbol":"AP003043.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103945548,"end":103946546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254242.1","gene_symbol":"AC100849.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19091733,"end":19115024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159186.4","gene_symbol":"AC007383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206236236,"end":206236871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165475.13","gene_symbol":"CRYL1","gene_name":"crystallin lambda 1 [Source:HGNC Symbol;Acc:HGNC:18246]","synonyms":"MGC149526,MGC149525,lambda-CRY,GDH","biotype":"protein_coding","ncbi_id":"51084","summary":"The uronate cycle functions as an alternative glucose metabolic pathway, accounting for about 5% of daily glucose catabolism. The product of this gene catalyzes the dehydrogenation of L-gulonate into dehydro-L-gulonate in the uronate cycle. The enzyme requires NAD(H) as a coenzyme, and is inhibited by inorganic phosphate. A similar gene in the rabbit is thought to serve a structural role in the lens of the eye. [provided by RefSeq, Jul 2008]","start":20403667,"end":20525857,"strand":-1,"description":"crystallin lambda 1 [Source:HGNC Symbol;Acc:HGNC:18246]"}, {"versioned_ensembl_gene_id":"ENSG00000006025.11","gene_symbol":"OSBPL7","gene_name":"oxysterol binding protein like 7 [Source:HGNC Symbol;Acc:HGNC:16387]","synonyms":"ORP7,MGC71150","biotype":"protein_coding","ncbi_id":"114881","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Like most members, the encoded protein contains an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. Two transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008]","start":47807372,"end":47821834,"strand":-1,"description":"oxysterol binding protein like 7 [Source:HGNC Symbol;Acc:HGNC:16387]"}, {"versioned_ensembl_gene_id":"ENSG00000237704.1","gene_symbol":"AP004289.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99340305,"end":99341761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255308.1","gene_symbol":"AC009652.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19196775,"end":19281426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104884.14","gene_symbol":"ERCC2","gene_name":"ERCC excision repair 2, TFIIH core complex helicase subunit [Source:HGNC Symbol;Acc:HGNC:3434]","synonyms":"MGC126219,MGC126218,MGC102762,MAG,EM9,XPD,TFIIH","biotype":"protein_coding","ncbi_id":"2068","summary":"The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":45349837,"end":45370918,"strand":-1,"description":"ERCC excision repair 2, TFIIH core complex helicase subunit [Source:HGNC Symbol;Acc:HGNC:3434]"}, {"versioned_ensembl_gene_id":"ENSG00000106823.12","gene_symbol":"ECM2","gene_name":"extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:3154]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1842","summary":"ECM2 encodes extracellular matrix protein 2, so named because it shares extensive similarity with known extracelluar matrix proteins. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":92493554,"end":92536655,"strand":-1,"description":"extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:3154]"}, {"versioned_ensembl_gene_id":"ENSG00000269154.1","gene_symbol":"BNIP3P13","gene_name":"BCL2 interacting protein 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060192","summary":null,"start":20062755,"end":20063320,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49693]"}, {"versioned_ensembl_gene_id":"ENSG00000225096.2","gene_symbol":"AL445250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57961438,"end":58438364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237025.1","gene_symbol":"AL121601.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123878590,"end":123879296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235731.1","gene_symbol":"LINC02250","gene_name":"long intergenic non-protein coding RNA 2250 [Source:HGNC Symbol;Acc:HGNC:53148]","synonyms":"TCONS_00023273","biotype":"lincRNA","ncbi_id":"105370737","summary":null,"start":25484831,"end":25578791,"strand":-1,"description":"long intergenic non-protein coding RNA 2250 [Source:HGNC Symbol;Acc:HGNC:53148]"}, {"versioned_ensembl_gene_id":"ENSG00000236431.1","gene_symbol":"AC009237.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95536117,"end":95536495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168490.13","gene_symbol":"PHYHIP","gene_name":"phytanoyl-CoA 2-hydroxylase interacting protein [Source:HGNC Symbol;Acc:HGNC:16865]","synonyms":"PAHX-AP,KIAA0273,DYRK1AP3","biotype":"protein_coding","ncbi_id":"9796","summary":null,"start":22219704,"end":22232341,"strand":-1,"description":"phytanoyl-CoA 2-hydroxylase interacting protein [Source:HGNC Symbol;Acc:HGNC:16865]"}, {"versioned_ensembl_gene_id":"ENSG00000153201.15","gene_symbol":"RANBP2","gene_name":"RAN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9848]","synonyms":"NUP358,ANE1,ADANE","biotype":"protein_coding","ncbi_id":"5903","summary":"RAN is a small GTP-binding protein of the RAS superfamily that is associated with the nuclear membrane and is thought to control a variety of cellular functions through its interactions with other proteins. This gene encodes a very large RAN-binding protein that immunolocalizes to the nuclear pore complex. The protein is a giant scaffold and mosaic cyclophilin-related nucleoporin implicated in the Ran-GTPase cycle. The encoded protein directly interacts with the E2 enzyme UBC9 and strongly enhances SUMO1 transfer from UBC9 to the SUMO1 target SP100. These findings place sumoylation at the cytoplasmic filaments of the nuclear pore complex and suggest that, for some substrates, modification and nuclear import are linked events. This gene is partially duplicated in a gene cluster that lies in a hot spot for recombination on chromosome 2q. [provided by RefSeq, Jul 2008]","start":108719481,"end":108785811,"strand":1,"description":"RAN binding protein 2 [Source:HGNC Symbol;Acc:HGNC:9848]"}, {"versioned_ensembl_gene_id":"ENSG00000228453.1","gene_symbol":"RPS15AP9","gene_name":"ribosomal protein S15a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441898","summary":null,"start":117138229,"end":117138609,"strand":1,"description":"ribosomal protein S15a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36164]"}, {"versioned_ensembl_gene_id":"ENSG00000256568.1","gene_symbol":"AP002761.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73176694,"end":73181696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253849.1","gene_symbol":"AC090539.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50381015,"end":50382275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167447.12","gene_symbol":"SMG8","gene_name":"SMG8, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:25551]","synonyms":"FLJ23205,FLJ10587,C17orf71","biotype":"protein_coding","ncbi_id":"55181","summary":null,"start":59209400,"end":59215247,"strand":1,"description":"SMG8, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:25551]"}, {"versioned_ensembl_gene_id":"ENSG00000234039.2","gene_symbol":"NDUFA5P7","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481784","summary":null,"start":86066227,"end":86066468,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48849]"}, {"versioned_ensembl_gene_id":"ENSG00000121716.20","gene_symbol":"PILRB","gene_name":"paired immunoglobin-like type 2 receptor beta [Source:HGNC Symbol;Acc:HGNC:18297]","synonyms":"FDFACT2,FDFACT1","biotype":"protein_coding","ncbi_id":"29990","summary":"The paired immunoglobin-like type 2 receptors consist of highly related activating and inhibitory receptors that are involved in the regulation of many aspects of the immune system. The paired immunoglobulin-like receptor genes are located in a tandem head-to-tail orientation on chromosome 7. This gene encodes the activating member of the receptor pair and contains a truncated cytoplasmic tail relative to its inhibitory counterpart (PILRA), that has a long cytoplasmic tail with immunoreceptor tyrosine-based inhibitory (ITIM) motifs. This gene is thought to have arisen from a duplication of the inhibitory PILRA gene and evolved to acquire its activating function. [provided by RefSeq, Jun 2013]","start":100352176,"end":100367733,"strand":1,"description":"paired immunoglobin-like type 2 receptor beta [Source:HGNC Symbol;Acc:HGNC:18297]"}, {"versioned_ensembl_gene_id":"ENSG00000173452.13","gene_symbol":"TMEM196","gene_name":"transmembrane protein 196 [Source:HGNC Symbol;Acc:HGNC:22431]","synonyms":"MGC42090","biotype":"protein_coding","ncbi_id":"256130","summary":null,"start":19719310,"end":19773598,"strand":-1,"description":"transmembrane protein 196 [Source:HGNC Symbol;Acc:HGNC:22431]"}, {"versioned_ensembl_gene_id":"ENSG00000161013.16","gene_symbol":"MGAT4B","gene_name":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:7048]","synonyms":"GnT-Ivb","biotype":"protein_coding","ncbi_id":"11282","summary":"This gene encodes a key glycosyltransferase that regulates the formation of tri- and multiantennary branching structures in the Golgi apparatus. The encoded protein, in addition to the related isoenzyme A, catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc in a beta-1,4 linkage to the Man-alpha-1,3-Man-beta-1,4-GlcNAc arm of R-Man-alpha-1,6(GlcNAc-beta-1,2-Man-alpha-1,3)Man-beta-1,4-GlcNAc-beta-1,4-GlcNAc-beta-1-Asn. The encoded protein may play a role in regulating the availability of serum glycoproteins, oncogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":179797597,"end":179806952,"strand":-1,"description":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:7048]"}, {"versioned_ensembl_gene_id":"ENSG00000105486.13","gene_symbol":"LIG1","gene_name":"DNA ligase 1 [Source:HGNC Symbol;Acc:HGNC:6598]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3978","summary":"This gene encodes a member of the ATP-dependent DNA ligase protein family. The encoded protein functions in DNA replication, recombination, and the base excision repair process. Mutations in this gene that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity to DNA-damaging agents. Disruption of this gene may also be associated with a variety of cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":48115445,"end":48170603,"strand":-1,"description":"DNA ligase 1 [Source:HGNC Symbol;Acc:HGNC:6598]"}, {"versioned_ensembl_gene_id":"ENSG00000223838.1","gene_symbol":"AC007091.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19353534,"end":19578606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253721.1","gene_symbol":"SUMO2P20","gene_name":"SUMO2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927327","summary":null,"start":69987415,"end":69987697,"strand":-1,"description":"SUMO2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49355]"}, {"versioned_ensembl_gene_id":"ENSG00000273090.1","gene_symbol":"AC007378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36513255,"end":36513732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253975.1","gene_symbol":"AC018861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62482198,"end":62483811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283064.1","gene_symbol":"AL353759.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26160765,"end":26172802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277224.2","gene_symbol":"HIST1H2BF","gene_name":"histone cluster 1 H2B family member f [Source:HGNC Symbol;Acc:HGNC:4752]","synonyms":"H2B/g,H2BFG","biotype":"protein_coding","ncbi_id":"8343","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. The protein has antibacterial and antifungal antimicrobial activity. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26199520,"end":26200715,"strand":1,"description":"histone cluster 1 H2B family member f [Source:HGNC Symbol;Acc:HGNC:4752]"}, {"versioned_ensembl_gene_id":"ENSG00000121743.3","gene_symbol":"GJA3","gene_name":"gap junction protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:4277]","synonyms":"CZP3,CX46","biotype":"protein_coding","ncbi_id":"2700","summary":"The protein encoded by this gene is a connexin and is a component of lens fiber gap junctions. Defects in this gene are a cause of zonular pulverulent cataract type 3 (CZP3). [provided by RefSeq, Jan 2010]","start":20138255,"end":20161049,"strand":-1,"description":"gap junction protein alpha 3 [Source:HGNC Symbol;Acc:HGNC:4277]"}, {"versioned_ensembl_gene_id":"ENSG00000115616.2","gene_symbol":"SLC9A2","gene_name":"solute carrier family 9 member A2 [Source:HGNC Symbol;Acc:HGNC:11072]","synonyms":"NHE2","biotype":"protein_coding","ncbi_id":"6549","summary":"This gene encodes a member of the sodium-hydrogen exchanger (NHE) protein family. These proteins are involved in sodium-ion transport by exchanging intracellular hydrogen ions to external sodium ions and help in the regulation of cell pH and volume. The encoded protein is localized to the apical membrane and is involved in apical absorption of sodium. [provided by RefSeq, Jun 2016]","start":102619707,"end":102711318,"strand":1,"description":"solute carrier family 9 member A2 [Source:HGNC Symbol;Acc:HGNC:11072]"}, {"versioned_ensembl_gene_id":"ENSG00000134901.12","gene_symbol":"KDELC1","gene_name":"KDEL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19350]","synonyms":"MGC5302,EP58","biotype":"protein_coding","ncbi_id":"79070","summary":"This gene encodes a protein product localized to the lumen of the endoplasmic reticulum. As a member of the endoplasmic reticulum protein family the encoded protein contains a Lys-Asp-Glu-Leu or KDEL motif located at the extreme C-terminus which prevents all endoplasmic reticulum resident proteins from being secreted. Proteins carrying this motif are bound by a receptor in the Golgi apparatus so that the receptor-ligand complex returns to the endoplasmic reticulum. A processed non-transcribed pseudogene located in an intron of a sodium transporter gene on chromosome 5 has been defined for this gene. This gene has multiple transcript variants which are predicted to encode distinct isoforms. [provided by RefSeq, Jan 2016]","start":102784281,"end":102799007,"strand":-1,"description":"KDEL motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19350]"}, {"versioned_ensembl_gene_id":"ENSG00000154309.8","gene_symbol":"DISP1","gene_name":"dispatched RND transporter family member 1 [Source:HGNC Symbol;Acc:HGNC:19711]","synonyms":"MGC16796,MGC13130,DKFZP434I0428,DISPA","biotype":"protein_coding","ncbi_id":"84976","summary":"The pattern of cellular proliferation and differentiation that leads to normal development of embryonic structures often depends upon the localized production of secreted protein signals. Cells surrounding the source of a particular signal respond in a graded manner according to the effective concentration of the signal, and this response produces the pattern of cell types constituting the mature structure. A novel segment-polarity gene known as dispatched has been identified in Drosophila and its protein product is required for normal Hedgehog (Hh) signaling. This gene is one of two human homologs of Drosophila dispatched and, based on sequence identity to its mouse counterpart, the encoded protein may play an essential role in Hh patterning activities in the early embryo. [provided by RefSeq, Jul 2008]","start":222872271,"end":223005995,"strand":1,"description":"dispatched RND transporter family member 1 [Source:HGNC Symbol;Acc:HGNC:19711]"}, {"versioned_ensembl_gene_id":"ENSG00000235978.6","gene_symbol":"AC018816.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4814294,"end":4887293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270255.1","gene_symbol":"AC009884.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19001627,"end":19001950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217770.1","gene_symbol":"FEM1AP3","gene_name":"fem-1 homolog A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643859","summary":null,"start":112365704,"end":112367444,"strand":-1,"description":"fem-1 homolog A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39831]"}, {"versioned_ensembl_gene_id":"ENSG00000206437.10","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"TNFC,p33,TNFSF3","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31570783,"end":31572750,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000270577.1","gene_symbol":"AC006023.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40115685,"end":40115943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227919.1","gene_symbol":"AL353997.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18452955,"end":18453062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135100.17","gene_symbol":"HNF1A","gene_name":"HNF1 homeobox A [Source:HGNC Symbol;Acc:HGNC:11621]","synonyms":"TCF1,MODY3,LFB1,HNF1","biotype":"protein_coding","ncbi_id":"6927","summary":"The protein encoded by this gene is a transcription factor required for the expression of several liver-specific genes. The encoded protein functions as a homodimer and binds to the inverted palindrome 5'-GTTAATNATTAAC-3'. Defects in this gene are a cause of maturity onset diabetes of the young type 3 (MODY3) and also can result in the appearance of hepatic adenomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":120978543,"end":121002512,"strand":1,"description":"HNF1 homeobox A [Source:HGNC Symbol;Acc:HGNC:11621]"}, {"versioned_ensembl_gene_id":"ENSG00000229689.3","gene_symbol":"AC009237.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95525345,"end":95532405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234693.1","gene_symbol":"AL353653.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50645471,"end":50662275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137812.19","gene_symbol":"KNL1","gene_name":"kinetochore scaffold 1 [Source:HGNC Symbol;Acc:HGNC:24054]","synonyms":"Spc7,PPP1R55,MCPH4,KIAA1570,hSpc105,hKNL-1,D40,CT29,CASC5,AF15Q14","biotype":"protein_coding","ncbi_id":"57082","summary":"The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jan 2013]","start":40594020,"end":40664342,"strand":1,"description":"kinetochore scaffold 1 [Source:HGNC Symbol;Acc:HGNC:24054]"}, {"versioned_ensembl_gene_id":"ENSG00000272148.1","gene_symbol":"AC013403.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27062428,"end":27062907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237810.3","gene_symbol":"AC104852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62143311,"end":62144769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275374.1","gene_symbol":"AC113385.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":100375700,"end":100381398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000028310.17","gene_symbol":"BRD9","gene_name":"bromodomain containing 9 [Source:HGNC Symbol;Acc:HGNC:25818]","synonyms":"FLJ13441","biotype":"protein_coding","ncbi_id":"65980","summary":null,"start":850291,"end":892824,"strand":-1,"description":"bromodomain containing 9 [Source:HGNC Symbol;Acc:HGNC:25818]"}, {"versioned_ensembl_gene_id":"ENSG00000182580.2","gene_symbol":"EPHB3","gene_name":"EPH receptor B3 [Source:HGNC Symbol;Acc:HGNC:3394]","synonyms":"Tyro6,Hek2,ETK2","biotype":"protein_coding","ncbi_id":"2049","summary":"Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are divided into two groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. This gene encodes a receptor for ephrin-B family members. [provided by RefSeq, Mar 2010]","start":184561784,"end":184582409,"strand":1,"description":"EPH receptor B3 [Source:HGNC Symbol;Acc:HGNC:3394]"}, {"versioned_ensembl_gene_id":"ENSG00000156011.16","gene_symbol":"PSD3","gene_name":"pleckstrin and Sec7 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19093]","synonyms":"KIAA0942,HCA67,EFA6R,EFA6D,DKFZp761K1423","biotype":"protein_coding","ncbi_id":"23362","summary":null,"start":18527301,"end":19084730,"strand":-1,"description":"pleckstrin and Sec7 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:19093]"}, {"versioned_ensembl_gene_id":"ENSG00000226904.1","gene_symbol":"AL353608.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68228651,"end":68229312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223863.1","gene_symbol":"LINC01805","gene_name":"long intergenic non-protein coding RNA 1805 [Source:HGNC Symbol;Acc:HGNC:52597]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374774","summary":null,"start":64486353,"end":64500904,"strand":1,"description":"long intergenic non-protein coding RNA 1805 [Source:HGNC Symbol;Acc:HGNC:52597]"}, {"versioned_ensembl_gene_id":"ENSG00000275647.1","gene_symbol":"AC093783.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128944628,"end":128944956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284737.1","gene_symbol":"BX649567.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67901099,"end":67920552,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260691.5","gene_symbol":"ANKRD20A1","gene_name":"ankyrin repeat domain 20 family member A1 [Source:HGNC Symbol;Acc:HGNC:23665]","synonyms":"DKFZp434A171,ANKRD20A","biotype":"protein_coding","ncbi_id":"84210","summary":null,"start":67859147,"end":67902094,"strand":1,"description":"ankyrin repeat domain 20 family member A1 [Source:HGNC Symbol;Acc:HGNC:23665]"}, {"versioned_ensembl_gene_id":"ENSG00000271207.1","gene_symbol":"MTCO1P22","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52087]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075165","summary":null,"start":100053686,"end":100055045,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52087]"}, {"versioned_ensembl_gene_id":"ENSG00000274265.4","gene_symbol":"AC245297.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149176022,"end":149251013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179600.3","gene_symbol":"GPHB5","gene_name":"glycoprotein hormone beta 5 [Source:HGNC Symbol;Acc:HGNC:18055]","synonyms":"ZLUT1,GPB5","biotype":"protein_coding","ncbi_id":"122876","summary":"GPHB5 is a cystine knot-forming polypeptide and a subunit of the dimeric glycoprotein hormone family (Hsu et al., 2002 [PubMed 12089349]).[supplied by OMIM, Mar 2008]","start":63312835,"end":63318879,"strand":-1,"description":"glycoprotein hormone beta 5 [Source:HGNC Symbol;Acc:HGNC:18055]"}, {"versioned_ensembl_gene_id":"ENSG00000237323.1","gene_symbol":"AC245036.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54652085,"end":54652230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249444.2","gene_symbol":"AC114324.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":99489559,"end":99499367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099385.11","gene_symbol":"BCL7C","gene_name":"BCL tumor suppressor 7C [Source:HGNC Symbol;Acc:HGNC:1006]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9274","summary":"This gene is identified by the similarity of its product to the N-terminal region of BCL7A protein. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. The function of this gene has not yet been determined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":30833626,"end":30894960,"strand":-1,"description":"BCL tumor suppressor 7C [Source:HGNC Symbol;Acc:HGNC:1006]"}, {"versioned_ensembl_gene_id":"ENSG00000144230.16","gene_symbol":"GPR17","gene_name":"G protein-coupled receptor 17 [Source:HGNC Symbol;Acc:HGNC:4471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2840","summary":null,"start":127645864,"end":127652639,"strand":1,"description":"G protein-coupled receptor 17 [Source:HGNC Symbol;Acc:HGNC:4471]"}, {"versioned_ensembl_gene_id":"ENSG00000260549.1","gene_symbol":"MT1L","gene_name":"metallothionein 1L, pseudogene [Source:HGNC Symbol;Acc:HGNC:7404]","synonyms":"MTF,MT1R,MT1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"4500","summary":null,"start":56617476,"end":56618818,"strand":1,"description":"metallothionein 1L, pseudogene [Source:HGNC Symbol;Acc:HGNC:7404]"}, {"versioned_ensembl_gene_id":"ENSG00000124818.15","gene_symbol":"OPN5","gene_name":"opsin 5 [Source:HGNC Symbol;Acc:HGNC:19992]","synonyms":"TMEM13,neuropsin,dJ402H5.1","biotype":"protein_coding","ncbi_id":"221391","summary":"Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This opsin gene is expressed in the eye, brain, testes, and spinal cord. This gene belongs to the seven-exon subfamily of mammalian opsin genes that includes peropsin (RRH) and retinal G protein coupled receptor (RGR). Like these other seven-exon opsin genes, this family member may encode a protein with photoisomerase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":47781982,"end":47832780,"strand":1,"description":"opsin 5 [Source:HGNC Symbol;Acc:HGNC:19992]"}, {"versioned_ensembl_gene_id":"ENSG00000273991.4","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR-8,CD85c,LIR8","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54251026,"end":54258210,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000254670.1","gene_symbol":"AC084859.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13001090,"end":13009159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220305.1","gene_symbol":"HNRNPH1P1","gene_name":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48751]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132803","summary":null,"start":159712801,"end":159713985,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48751]"}, {"versioned_ensembl_gene_id":"ENSG00000170430.9","gene_symbol":"MGMT","gene_name":"O-6-methylguanine-DNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:7059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4255","summary":"Alkylating agents are potent carcinogens that can result in cell death, mutation and cancer. The protein encoded by this gene is a DNA repair protein that is involved in cellular defense against mutagenesis and toxicity from alkylating agents. The protein catalyzes transfer of methyl groups from O(6)-alkylguanine and other methylated moieties of the DNA to its own molecule, which repairs the toxic lesions. Methylation of the genes promoter has been associated with several cancer types, including colorectal cancer, lung cancer, lymphoma and glioblastoma. [provided by RefSeq, Sep 2015]","start":129467184,"end":129768007,"strand":1,"description":"O-6-methylguanine-DNA methyltransferase [Source:HGNC Symbol;Acc:HGNC:7059]"}, {"versioned_ensembl_gene_id":"ENSG00000188523.8","gene_symbol":"CFAP77","gene_name":"cilia and flagella associated protein 77 [Source:HGNC Symbol;Acc:HGNC:33776]","synonyms":"FLJ46082,C9orf171","biotype":"protein_coding","ncbi_id":"389799","summary":null,"start":132410043,"end":132573317,"strand":1,"description":"cilia and flagella associated protein 77 [Source:HGNC Symbol;Acc:HGNC:33776]"}, {"versioned_ensembl_gene_id":"ENSG00000163444.11","gene_symbol":"TMEM183A","gene_name":"transmembrane protein 183A [Source:HGNC Symbol;Acc:HGNC:20173]","synonyms":"C1orf37","biotype":"protein_coding","ncbi_id":"92703","summary":null,"start":203007386,"end":203024848,"strand":1,"description":"transmembrane protein 183A [Source:HGNC Symbol;Acc:HGNC:20173]"}, {"versioned_ensembl_gene_id":"ENSG00000272494.1","gene_symbol":"OR1X1P","gene_name":"olfactory receptor family 1 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15062]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402236","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":176006145,"end":176007387,"strand":1,"description":"olfactory receptor family 1 subfamily X member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15062]"}, {"versioned_ensembl_gene_id":"ENSG00000180869.4","gene_symbol":"LINC01555","gene_name":"long intergenic non-protein coding RNA 1555 [Source:HGNC Symbol;Acc:HGNC:26647]","synonyms":"C1orf180,FLJ35487","biotype":"lincRNA","ncbi_id":"439927","summary":null,"start":84628230,"end":84635020,"strand":-1,"description":"long intergenic non-protein coding RNA 1555 [Source:HGNC Symbol;Acc:HGNC:26647]"}, {"versioned_ensembl_gene_id":"ENSG00000087995.15","gene_symbol":"METTL2A","gene_name":"methyltransferase like 2A [Source:HGNC Symbol;Acc:HGNC:25755]","synonyms":"METTL2,FLJ12760","biotype":"protein_coding","ncbi_id":"339175","summary":null,"start":62423867,"end":62450822,"strand":1,"description":"methyltransferase like 2A [Source:HGNC Symbol;Acc:HGNC:25755]"}, {"versioned_ensembl_gene_id":"ENSG00000259546.1","gene_symbol":"AC027808.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80896190,"end":80948867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254895.2","gene_symbol":"MTCO3P15","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52045]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075154","summary":null,"start":103402013,"end":103402586,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:52045]"}, {"versioned_ensembl_gene_id":"ENSG00000183185.9","gene_symbol":"GABRR3","gene_name":"gamma-aminobutyric acid type A receptor rho3 subunit (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:17969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200959","summary":"The neurotransmitter gamma-aminobutyric acid (GABA) functions in the central nervous system to regulate synaptic transmission of neurons. This gene encodes one of three related subunits, which combine as homo- or hetero-pentamers to form GABA(C) receptors. In humans, some individuals contain a single-base polymorphism (dbSNP rs832032) that is predicted to inactivate the gene product. [provided by RefSeq, Jan 2012]","start":97986673,"end":98035304,"strand":-1,"description":"gamma-aminobutyric acid type A receptor rho3 subunit (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:17969]"}, {"versioned_ensembl_gene_id":"ENSG00000250313.2","gene_symbol":"LINC02229","gene_name":"long intergenic non-protein coding RNA 2229 [Source:HGNC Symbol;Acc:HGNC:53098]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928769","summary":null,"start":66507544,"end":66511604,"strand":-1,"description":"long intergenic non-protein coding RNA 2229 [Source:HGNC Symbol;Acc:HGNC:53098]"}, {"versioned_ensembl_gene_id":"ENSG00000213137.3","gene_symbol":"ARF1P2","gene_name":"ADP ribosylation factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39883]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420012","summary":null,"start":120845110,"end":120845647,"strand":-1,"description":"ADP ribosylation factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39883]"}, {"versioned_ensembl_gene_id":"ENSG00000258638.2","gene_symbol":"AL389895.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62514872,"end":62515123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255393.1","gene_symbol":"AP000790.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60024908,"end":60031077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250725.2","gene_symbol":"AC080079.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165664350,"end":165665671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233089.6","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32883358,"end":32885767,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000164920.9","gene_symbol":"OSR2","gene_name":"odd-skipped related transciption factor 2 [Source:HGNC Symbol;Acc:HGNC:15830]","synonyms":"FLJ90037","biotype":"protein_coding","ncbi_id":"116039","summary":"OSR2 is a mammalian homolog of the Drosophila odd-skipped family of transcription factors (Lan et al., 2004 [PubMed 15175245]).[supplied by OMIM, Mar 2008]","start":98944403,"end":98952104,"strand":1,"description":"odd-skipped related transciption factor 2 [Source:HGNC Symbol;Acc:HGNC:15830]"}, {"versioned_ensembl_gene_id":"ENSG00000248515.1","gene_symbol":"AC024230.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19455436,"end":19909692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198960.10","gene_symbol":"ARMCX6","gene_name":"armadillo repeat containing, X-linked 6 [Source:HGNC Symbol;Acc:HGNC:26094]","synonyms":"GASP10,FLJ20811","biotype":"protein_coding","ncbi_id":"54470","summary":null,"start":101615118,"end":101618001,"strand":-1,"description":"armadillo repeat containing, X-linked 6 [Source:HGNC Symbol;Acc:HGNC:26094]"}, {"versioned_ensembl_gene_id":"ENSG00000242861.1","gene_symbol":"AL591895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":225840883,"end":225846522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136709.11","gene_symbol":"WDR33","gene_name":"WD repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:25651]","synonyms":"WDC146,NET14,FLJ11294","biotype":"protein_coding","ncbi_id":"55339","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is highly expressed in testis and the protein is localized to the nucleus. This gene may play important roles in the mechanisms of cytodifferentiation and/or DNA recombination. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":127701022,"end":127811187,"strand":-1,"description":"WD repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:25651]"}, {"versioned_ensembl_gene_id":"ENSG00000244002.1","gene_symbol":"RPSAP39","gene_name":"ribosomal protein SA pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37040]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131161","summary":null,"start":80161129,"end":80162011,"strand":1,"description":"ribosomal protein SA pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37040]"}, {"versioned_ensembl_gene_id":"ENSG00000203386.6","gene_symbol":"LINC01317","gene_name":"long intergenic non-protein coding RNA 1317 [Source:HGNC Symbol;Acc:HGNC:50523]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355287","summary":null,"start":33706886,"end":34297753,"strand":1,"description":"long intergenic non-protein coding RNA 1317 [Source:HGNC Symbol;Acc:HGNC:50523]"}, {"versioned_ensembl_gene_id":"ENSG00000228554.1","gene_symbol":"AC004837.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39700341,"end":39703296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006451.7","gene_symbol":"RALA","gene_name":"RAS like proto-oncogene A [Source:HGNC Symbol;Acc:HGNC:9839]","synonyms":"RAL","biotype":"protein_coding","ncbi_id":"5898","summary":"The product of this gene belongs to the small GTPase superfamily, Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. This gene encodes a low molecular mass ras-like GTP-binding protein that shares about 50% similarity with other ras proteins. [provided by RefSeq, Jul 2008]","start":39623483,"end":39708124,"strand":1,"description":"RAS like proto-oncogene A [Source:HGNC Symbol;Acc:HGNC:9839]"}, {"versioned_ensembl_gene_id":"ENSG00000253810.1","gene_symbol":"PSAT1P1","gene_name":"phosphoserine aminotransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15785]","synonyms":"C8orf62","biotype":"processed_pseudogene","ncbi_id":"137133","summary":null,"start":49740216,"end":49741321,"strand":-1,"description":"phosphoserine aminotransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15785]"}, {"versioned_ensembl_gene_id":"ENSG00000204778.4","gene_symbol":"CBWD4P","gene_name":"COBW domain containing 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:18520]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653510","summary":null,"start":65287914,"end":65323015,"strand":-1,"description":"COBW domain containing 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:18520]"}, {"versioned_ensembl_gene_id":"ENSG00000111537.4","gene_symbol":"IFNG","gene_name":"interferon gamma [Source:HGNC Symbol;Acc:HGNC:5438]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3458","summary":"This gene encodes a soluble cytokine that is a member of the type II interferon class. The encoded protein is secreted by cells of both the innate and adaptive immune systems. The active protein is a homodimer that binds to the interferon gamma receptor which triggers a cellular response to viral and microbial infections. Mutations in this gene are associated with an increased susceptibility to viral, bacterial and parasitic infections and to several autoimmune diseases. [provided by RefSeq, Dec 2015]","start":68154768,"end":68159747,"strand":-1,"description":"interferon gamma [Source:HGNC Symbol;Acc:HGNC:5438]"}, {"versioned_ensembl_gene_id":"ENSG00000267185.1","gene_symbol":"AC067852.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42533532,"end":42534009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123427.16","gene_symbol":"EEF1AKMT3","gene_name":"EEF1A lysine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:24936]","synonyms":"METTL21B,FAM119B,DKFZP586D0919","biotype":"protein_coding","ncbi_id":"25895","summary":null,"start":57771492,"end":57782541,"strand":1,"description":"EEF1A lysine methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:24936]"}, {"versioned_ensembl_gene_id":"ENSG00000253615.1","gene_symbol":"AC069113.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27903566,"end":27903715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282798.1","gene_symbol":"AC008993.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":69167,"end":69972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267255.1","gene_symbol":"AC011498.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4429689,"end":4430934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277440.1","gene_symbol":"AC012676.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4430522,"end":4431103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225589.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"KIAA0170,Em:AB023051.5,NFBD1","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30690066,"end":30708147,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000227934.1","gene_symbol":"AL732414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231021611,"end":231022183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112378.11","gene_symbol":"PERP","gene_name":"PERP, TP53 apoptosis effector [Source:HGNC Symbol;Acc:HGNC:17637]","synonyms":"KCP1,dJ496H19.1,THW,PIGPC1,KRTCAP1","biotype":"protein_coding","ncbi_id":"64065","summary":null,"start":138088505,"end":138107511,"strand":-1,"description":"PERP, TP53 apoptosis effector [Source:HGNC Symbol;Acc:HGNC:17637]"}, {"versioned_ensembl_gene_id":"ENSG00000219463.1","gene_symbol":"RPSAP42","gene_name":"ribosomal protein SA pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36265]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270919","summary":null,"start":137995270,"end":137996147,"strand":1,"description":"ribosomal protein SA pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36265]"}, {"versioned_ensembl_gene_id":"ENSG00000250378.2","gene_symbol":"AC114296.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":135812667,"end":135826584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239988.1","gene_symbol":"RPL31P60","gene_name":"ribosomal protein L31 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:36123]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271486","summary":null,"start":32963499,"end":32963865,"strand":1,"description":"ribosomal protein L31 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:36123]"}, {"versioned_ensembl_gene_id":"ENSG00000188322.4","gene_symbol":"SBK1","gene_name":"SH3 domain binding kinase 1 [Source:HGNC Symbol;Acc:HGNC:17699]","synonyms":"Sbk","biotype":"protein_coding","ncbi_id":"388228","summary":null,"start":28292519,"end":28323849,"strand":1,"description":"SH3 domain binding kinase 1 [Source:HGNC Symbol;Acc:HGNC:17699]"}, {"versioned_ensembl_gene_id":"ENSG00000280323.1","gene_symbol":"AC053503.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":219427477,"end":219429319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249198.1","gene_symbol":"AC106822.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57751192,"end":57751717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174136.11","gene_symbol":"RGMB","gene_name":"repulsive guidance molecule family member b [Source:HGNC Symbol;Acc:HGNC:26896]","synonyms":"FLJ90406,DRAGON","biotype":"protein_coding","ncbi_id":"285704","summary":"RGMB is a glycosylphosphatidylinositol (GPI)-anchored member of the repulsive guidance molecule family (see RGMA, MIM 607362) and contributes to the patterning of the developing nervous system (Samad et al., 2005 [PubMed 15671031]).[supplied by OMIM, Apr 2009]","start":98768650,"end":98798643,"strand":1,"description":"repulsive guidance molecule family member b [Source:HGNC Symbol;Acc:HGNC:26896]"}, {"versioned_ensembl_gene_id":"ENSG00000118369.12","gene_symbol":"USP35","gene_name":"ubiquitin specific peptidase 35 [Source:HGNC Symbol;Acc:HGNC:20061]","synonyms":"KIAA1372","biotype":"protein_coding","ncbi_id":"57558","summary":"This gene encodes a member of the peptidase C19 family of ubiquitin-specific proteases. These deubiquitinating enzymes (DUBs) catalyze the removal of ubiquitin proteins from other proteins. The encoded protein associates with polarized mitochondria and has been shown to inhibit NF-kappa B activation and delay PARK2-mediated degradation of mitochondria. Expression of this gene is upregulated by the let-7a microRNA and reduced expression has been observed in human tumor tissues. [provided by RefSeq, Jul 2017]","start":78188812,"end":78214711,"strand":1,"description":"ubiquitin specific peptidase 35 [Source:HGNC Symbol;Acc:HGNC:20061]"}, {"versioned_ensembl_gene_id":"ENSG00000279232.2","gene_symbol":"AC008522.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98792861,"end":98795766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235256.1","gene_symbol":"FKBP4P7","gene_name":"FK506 binding protein 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50376]","synonyms":"FKBP4P3","biotype":"processed_pseudogene","ncbi_id":"441410","summary":null,"start":62710036,"end":62711398,"strand":-1,"description":"FK506 binding protein 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50376]"}, {"versioned_ensembl_gene_id":"ENSG00000172379.20","gene_symbol":"ARNT2","gene_name":"aryl hydrocarbon receptor nuclear translocator 2 [Source:HGNC Symbol;Acc:HGNC:16876]","synonyms":"KIAA0307,bHLHe1","biotype":"protein_coding","ncbi_id":"9915","summary":"This gene encodes a member of the basic-helix-loop-helix-Per-Arnt-Sim (bHLH-PAS) superfamily of transcription factors. The encoded protein acts as a partner for several sensor proteins of the bHLH-PAS family, forming heterodimers with the sensor proteins that bind regulatory DNA sequences in genes responsive to developmental and environmental stimuli. Under hypoxic conditions, the encoded protein complexes with hypoxia-inducible factor 1alpha in the nucleus and this complex binds to hypoxia-responsive elements in enhancers and promoters of oxygen-responsive genes. A highly similar protein in mouse forms functional complexes with both aryl hydrocarbon receptors and Single-minded proteins, suggesting additional roles for the encoded protein in the metabolism of xenobiotic compounds and the regulation of neurogenesis, respectively. [provided by RefSeq, Dec 2013]","start":80404350,"end":80597937,"strand":1,"description":"aryl hydrocarbon receptor nuclear translocator 2 [Source:HGNC Symbol;Acc:HGNC:16876]"}, {"versioned_ensembl_gene_id":"ENSG00000178177.15","gene_symbol":"LCORL","gene_name":"ligand dependent nuclear receptor corepressor like [Source:HGNC Symbol;Acc:HGNC:30776]","synonyms":"MLR1,FLJ30696","biotype":"protein_coding","ncbi_id":"254251","summary":"This gene encodes a transcription factor that appears to function in spermatogenesis. Polymorphisms in this gene are associated with measures of skeletal frame size and adult height. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":17841199,"end":18021876,"strand":-1,"description":"ligand dependent nuclear receptor corepressor like [Source:HGNC Symbol;Acc:HGNC:30776]"}, {"versioned_ensembl_gene_id":"ENSG00000230887.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30493160,"end":30497764,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000273540.3","gene_symbol":"AGBL1","gene_name":"ATP/GTP binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:26504]","synonyms":"FLJ32310,CCP4","biotype":"protein_coding","ncbi_id":"123624","summary":"Polyglutamylation is a reversible posttranslational modification catalyzed by polyglutamylases that results in the addition of glutamate side chains on the modified protein. This gene encodes a glutamate decarboxylase that catalyzes the deglutamylation of polyglutamylated proteins. Mutations in this gene result in dominant late-onset Fuchs corneal dystrophy. [provided by RefSeq, Nov 2013]","start":86079973,"end":87029052,"strand":1,"description":"ATP/GTP binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:26504]"}, {"versioned_ensembl_gene_id":"ENSG00000198795.10","gene_symbol":"ZNF521","gene_name":"zinc finger protein 521 [Source:HGNC Symbol;Acc:HGNC:24605]","synonyms":"Evi3,EHZF","biotype":"protein_coding","ncbi_id":"25925","summary":null,"start":25061926,"end":25352190,"strand":-1,"description":"zinc finger protein 521 [Source:HGNC Symbol;Acc:HGNC:24605]"}, {"versioned_ensembl_gene_id":"ENSG00000273513.1","gene_symbol":"TBC1D3K","gene_name":"TBC1 domain family member 3K [Source:HGNC Symbol;Acc:HGNC:51245]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060351","summary":null,"start":37924415,"end":37935365,"strand":1,"description":"TBC1 domain family member 3K [Source:HGNC Symbol;Acc:HGNC:51245]"}, {"versioned_ensembl_gene_id":"ENSG00000271225.1","gene_symbol":"BNIP3P4","gene_name":"BCL2 interacting protein 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39657]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289028","summary":null,"start":64810865,"end":64811429,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39657]"}, {"versioned_ensembl_gene_id":"ENSG00000230982.1","gene_symbol":"DSTNP1","gene_name":"destrin, actin depolymerizing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23769]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387492","summary":null,"start":46653558,"end":46654022,"strand":-1,"description":"destrin, actin depolymerizing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23769]"}, {"versioned_ensembl_gene_id":"ENSG00000235932.2","gene_symbol":"AL359955.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64737403,"end":64737755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250167.1","gene_symbol":"AC034206.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135559577,"end":135634874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138175.8","gene_symbol":"ARL3","gene_name":"ADP ribosylation factor like GTPase 3 [Source:HGNC Symbol;Acc:HGNC:694]","synonyms":"ARFL3","biotype":"protein_coding","ncbi_id":"403","summary":"ADP-ribosylation factor-like 3 is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL3 binds guanine nucleotides but lacks ADP-ribosylation factor activity. [provided by RefSeq, Jul 2008]","start":102673731,"end":102714407,"strand":-1,"description":"ADP ribosylation factor like GTPase 3 [Source:HGNC Symbol;Acc:HGNC:694]"}, {"versioned_ensembl_gene_id":"ENSG00000181965.5","gene_symbol":"NEUROG1","gene_name":"neurogenin 1 [Source:HGNC Symbol;Acc:HGNC:7764]","synonyms":"ngn1,NEUROD3,Math4C,bHLHa6,AKA","biotype":"protein_coding","ncbi_id":"4762","summary":null,"start":135534282,"end":135535949,"strand":-1,"description":"neurogenin 1 [Source:HGNC Symbol;Acc:HGNC:7764]"}, {"versioned_ensembl_gene_id":"ENSG00000225883.2","gene_symbol":"BMS1P11","gene_name":"BMS1, ribosome biogenesis factor pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49156]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644632","summary":null,"start":64705734,"end":64709311,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49156]"}, {"versioned_ensembl_gene_id":"ENSG00000235310.1","gene_symbol":"GXYLT1P6","gene_name":"glucoside xylosyltransferase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50425]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132672","summary":null,"start":64488600,"end":64489786,"strand":1,"description":"glucoside xylosyltransferase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50425]"}, {"versioned_ensembl_gene_id":"ENSG00000272750.1","gene_symbol":"AL592148.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":222658867,"end":222661512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114127.10","gene_symbol":"XRN1","gene_name":"5'-3' exoribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:30654]","synonyms":"SEP1","biotype":"protein_coding","ncbi_id":"54464","summary":"This gene encodes a member of the 5'-3' exonuclease family. The encoded protein may be involved in replication-dependent histone mRNA degradation, and interacts directly with the enhancer of mRNA-decapping protein 4. In addition to mRNA metabolism, a similar protein in yeast has been implicated in a variety of nuclear and cytoplasmic functions, including homologous recombination, meiosis, telomere maintenance, and microtubule assembly. Mutations in this gene are associated with osteosarcoma, suggesting that the encoded protein may also play a role in bone formation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":142306607,"end":142448062,"strand":-1,"description":"5'-3' exoribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:30654]"}, {"versioned_ensembl_gene_id":"ENSG00000214517.9","gene_symbol":"PPME1","gene_name":"protein phosphatase methylesterase 1 [Source:HGNC Symbol;Acc:HGNC:30178]","synonyms":"PME-1","biotype":"protein_coding","ncbi_id":"51400","summary":"This gene encodes a protein phosphatase methylesterase localized to the nucleus. The encoded protein acts on the protein phosphatase-2A catalytic subunit and supports the ERK pathway through dephosphorylation of regulatory proteins. It plays a role in malignant glioma progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":74171099,"end":74254703,"strand":1,"description":"protein phosphatase methylesterase 1 [Source:HGNC Symbol;Acc:HGNC:30178]"}, {"versioned_ensembl_gene_id":"ENSG00000184599.13","gene_symbol":"FAM19A3","gene_name":"family with sequence similarity 19 member A3, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21590]","synonyms":"TAFA3,TAFA-3","biotype":"protein_coding","ncbi_id":"284467","summary":"This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines, that act as regulators of immune and nervous cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":112720419,"end":112727235,"strand":1,"description":"family with sequence similarity 19 member A3, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21590]"}, {"versioned_ensembl_gene_id":"ENSG00000138757.14","gene_symbol":"G3BP2","gene_name":"G3BP stress granule assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:30291]","synonyms":"KIAA0660","biotype":"protein_coding","ncbi_id":"9908","summary":null,"start":75642782,"end":75724525,"strand":-1,"description":"G3BP stress granule assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:30291]"}, {"versioned_ensembl_gene_id":"ENSG00000280069.1","gene_symbol":"AC127024.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30738182,"end":30740275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065135.10","gene_symbol":"GNAI3","gene_name":"G protein subunit alpha i3 [Source:HGNC Symbol;Acc:HGNC:4387]","synonyms":"87U6","biotype":"protein_coding","ncbi_id":"2773","summary":"Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling pathways. G proteins are composed of 3 units: alpha, beta and gamma. This gene encodes an alpha subunit and belongs to the G-alpha family. Mutation in this gene, resulting in a gly40-to-arg substitution, is associated with auriculocondylar syndrome, and shown to affect downstream targets in the G protein-coupled endothelin receptor pathway. [provided by RefSeq, Jun 2012]","start":109548611,"end":109618321,"strand":1,"description":"G protein subunit alpha i3 [Source:HGNC Symbol;Acc:HGNC:4387]"}, {"versioned_ensembl_gene_id":"ENSG00000204308.7","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"RING5,RMA1,NG2,G16","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32178354,"end":32180793,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000244451.1","gene_symbol":"AP003041.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130082495,"end":130082781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256351.1","gene_symbol":"AC007834.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109859767,"end":109860420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170854.17","gene_symbol":"RIOX2","gene_name":"ribosomal oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:19441]","synonyms":"NO52,MINA53,MINA,mdig,JMJD10,FLJ14393","biotype":"protein_coding","ncbi_id":"84864","summary":"MINA is a c-Myc (MYC; MIM 190080) target gene that may play a role in cell proliferation or regulation of cell growth. (Tsuneoka et al., 2002 [PubMed 12091391]; Zhang et al., 2005 [PubMed 15897898]).[supplied by OMIM, May 2008]","start":97941818,"end":97972457,"strand":-1,"description":"ribosomal oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:19441]"}, {"versioned_ensembl_gene_id":"ENSG00000101251.11","gene_symbol":"SEL1L2","gene_name":"SEL1L2 ERAD E3 ligase adaptor subunit [Source:HGNC Symbol;Acc:HGNC:15897]","synonyms":"DKFZp434C1826,C20orf50","biotype":"protein_coding","ncbi_id":"80343","summary":null,"start":13849247,"end":13996443,"strand":-1,"description":"SEL1L2 ERAD E3 ligase adaptor subunit [Source:HGNC Symbol;Acc:HGNC:15897]"}, {"versioned_ensembl_gene_id":"ENSG00000282065.1","gene_symbol":"IGHJ4","gene_name":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28477","summary":null,"start":105864986,"end":105865033,"strand":-1,"description":"immunoglobulin heavy joining 4 [Source:HGNC Symbol;Acc:HGNC:5538]"}, {"versioned_ensembl_gene_id":"ENSG00000223576.2","gene_symbol":"AL355001.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19841827,"end":19843672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254035.1","gene_symbol":"AC104117.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178969390,"end":178990116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276358.2","gene_symbol":"PLEKHM1","gene_name":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]","synonyms":"KIAA0356","biotype":"protein_coding","ncbi_id":"9842","summary":"The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":45435902,"end":45490401,"strand":-1,"description":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]"}, {"versioned_ensembl_gene_id":"ENSG00000258984.5","gene_symbol":"UBE2F-SCLY","gene_name":"UBE2F-SCLY readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48339]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533179","summary":"This locus represents naturally occurring read-through transcription between the neighboring UBE2F (ubiquitin-conjugating enzyme E2F) and SCLY (selenocysteine lyase) genes on chromosome 2. The read-through transcript is a candidate for non-sense mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":237967014,"end":238099412,"strand":1,"description":"UBE2F-SCLY readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48339]"}, {"versioned_ensembl_gene_id":"ENSG00000275419.1","gene_symbol":"AL357075.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154542552,"end":154542740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229444.1","gene_symbol":"AL451062.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43709392,"end":43727343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226182.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31573530,"end":31576311,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000270553.1","gene_symbol":"AC011921.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60513190,"end":60513550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231984.1","gene_symbol":"AL596266.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199752491,"end":199752890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000026036.21","gene_symbol":"RTEL1-TNFRSF6B","gene_name":"RTEL1-TNFRSF6B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44095]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533107","summary":"This locus represents naturally occurring read-through transcription between the neighboring RTEL1 (regulator of telomere elongation helicase 1) and TNFRSF6B (tumor necrosis factor receptor superfamily, member 6b, decoy) genes on chromosome 20. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":63659300,"end":63698684,"strand":1,"description":"RTEL1-TNFRSF6B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44095]"}, {"versioned_ensembl_gene_id":"ENSG00000266520.1","gene_symbol":"AC022884.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24685772,"end":24686351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127334.10","gene_symbol":"DYRK2","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 2 [Source:HGNC Symbol;Acc:HGNC:3093]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8445","summary":" DYRK2 belongs to a family of protein kinases whose members are presumed to be involved in cellular growth and/or development. The family is defined by structural similarity of their kinase domains and their capability to autophosphorylate on tyrosine residues. DYRK2 has demonstrated tyrosine autophosphorylation and catalyzed phosphorylation of histones H3 and H2B in vitro. Two isoforms of DYRK2 have been isolated. The predominant isoform, isoform 1, lacks a 5' terminal insert. [provided by RefSeq, Jul 2008]","start":67648338,"end":67665406,"strand":1,"description":"dual specificity tyrosine phosphorylation regulated kinase 2 [Source:HGNC Symbol;Acc:HGNC:3093]"}, {"versioned_ensembl_gene_id":"ENSG00000235872.2","gene_symbol":"AC078777.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67658991,"end":67670919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248750.2","gene_symbol":"AC020699.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92884663,"end":92885107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271894.1","gene_symbol":"AC007744.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":56147630,"end":56386171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250908.1","gene_symbol":"AC110800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93318623,"end":93319786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134489.6","gene_symbol":"HRH4","gene_name":"histamine receptor H4 [Source:HGNC Symbol;Acc:HGNC:17383]","synonyms":"AXOR35,HH4R,H4R,GPRv53,GPCR105","biotype":"protein_coding","ncbi_id":"59340","summary":"Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. Its various actions are mediated by a family of histamine receptors, which are a subset of the G-protein coupled receptor superfamily. This gene encodes a histamine receptor that is predominantly expressed in haematopoietic cells. The protein is thought to play a role in inflammation and allergy reponses. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":24460629,"end":24479957,"strand":1,"description":"histamine receptor H4 [Source:HGNC Symbol;Acc:HGNC:17383]"}, {"versioned_ensembl_gene_id":"ENSG00000249592.5","gene_symbol":"AC139887.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":762387,"end":781849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233799.1","gene_symbol":"AC139887.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":764487,"end":765074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230635.2","gene_symbol":"CYP4F60P","gene_name":"cytochrome P450 family 4 subfamily F member 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:42468]","synonyms":"CYP4F-se15[6:7:8]","biotype":"unprocessed_pseudogene","ncbi_id":"107126294","summary":null,"start":42950566,"end":42951630,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 60, pseudogene [Source:HGNC Symbol;Acc:HGNC:42468]"}, {"versioned_ensembl_gene_id":"ENSG00000141759.14","gene_symbol":"TXNL4A","gene_name":"thioredoxin like 4A [Source:HGNC Symbol;Acc:HGNC:30551]","synonyms":"U5-15kD,TXNL4,SNRNP15,HsT161,DIM1,DIB1","biotype":"protein_coding","ncbi_id":"10907","summary":"The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":79970811,"end":80033949,"strand":-1,"description":"thioredoxin like 4A [Source:HGNC Symbol;Acc:HGNC:30551]"}, {"versioned_ensembl_gene_id":"ENSG00000272829.1","gene_symbol":"AC002470.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20981361,"end":20981755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272588.1","gene_symbol":"AC139887.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":757022,"end":757740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230558.2","gene_symbol":"CEACAMP2","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1824]","synonyms":"CGM9","biotype":"unprocessed_pseudogene","ncbi_id":"1091","summary":null,"start":42560433,"end":42561750,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1824]"}, {"versioned_ensembl_gene_id":"ENSG00000233559.1","gene_symbol":"LINC00513","gene_name":"long intergenic non-protein coding RNA 513 [Source:HGNC Symbol;Acc:HGNC:43566]","synonyms":"AC016831.7","biotype":"lincRNA","ncbi_id":"100506860","summary":null,"start":130853720,"end":130928649,"strand":1,"description":"long intergenic non-protein coding RNA 513 [Source:HGNC Symbol;Acc:HGNC:43566]"}, {"versioned_ensembl_gene_id":"ENSG00000249052.1","gene_symbol":"AC093810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91887886,"end":91904335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111911.6","gene_symbol":"HINT3","gene_name":"histidine triad nucleotide binding protein 3 [Source:HGNC Symbol;Acc:HGNC:18468]","synonyms":"FLJ33126","biotype":"protein_coding","ncbi_id":"135114","summary":"Histidine triad proteins, such as HINT3, are nucleotide hydrolases and transferases that act on the alpha-phosphate of ribonucleotides (Brenner, 2002 [PubMed 12119013]).[supplied by OMIM, Mar 2008]","start":125956781,"end":125980244,"strand":1,"description":"histidine triad nucleotide binding protein 3 [Source:HGNC Symbol;Acc:HGNC:18468]"}, {"versioned_ensembl_gene_id":"ENSG00000258534.1","gene_symbol":"AL132712.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103854366,"end":103880111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258735.1","gene_symbol":"LINC00637","gene_name":"long intergenic non-protein coding RNA 637 [Source:HGNC Symbol;Acc:HGNC:27069]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145216","summary":null,"start":103847721,"end":103858049,"strand":1,"description":"long intergenic non-protein coding RNA 637 [Source:HGNC Symbol;Acc:HGNC:27069]"}, {"versioned_ensembl_gene_id":"ENSG00000261325.1","gene_symbol":"LINC02192","gene_name":"long intergenic non-protein coding RNA 2192 [Source:HGNC Symbol;Acc:HGNC:53054]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507534","summary":null,"start":47849314,"end":47887130,"strand":-1,"description":"long intergenic non-protein coding RNA 2192 [Source:HGNC Symbol;Acc:HGNC:53054]"}, {"versioned_ensembl_gene_id":"ENSG00000185619.18","gene_symbol":"PCGF3","gene_name":"polycomb group ring finger 3 [Source:HGNC Symbol;Acc:HGNC:10066]","synonyms":"RNF3A,RNF3,MGC40413,FLJ36550,DONG1","biotype":"protein_coding","ncbi_id":"10336","summary":"The protein encoded by this gene contains a C3HC4 type RING finger, which is a motif known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. [provided by RefSeq, Jul 2008]","start":705748,"end":770640,"strand":1,"description":"polycomb group ring finger 3 [Source:HGNC Symbol;Acc:HGNC:10066]"}, {"versioned_ensembl_gene_id":"ENSG00000236736.1","gene_symbol":"UQCRC2P1","gene_name":"ubiquinol-cytochrome c reductase core protein II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44309]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131327","summary":null,"start":46310591,"end":46311922,"strand":-1,"description":"ubiquinol-cytochrome c reductase core protein II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44309]"}, {"versioned_ensembl_gene_id":"ENSG00000232815.1","gene_symbol":"DUX4L50","gene_name":"double homeobox 4 like 50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51788]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480350","summary":null,"start":63817748,"end":63818462,"strand":-1,"description":"double homeobox 4 like 50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51788]"}, {"versioned_ensembl_gene_id":"ENSG00000228179.1","gene_symbol":"HLA-S","gene_name":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]","synonyms":"HLA-17","biotype":"unprocessed_pseudogene","ncbi_id":"267015","summary":null,"start":31425088,"end":31425302,"strand":-1,"description":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]"}, {"versioned_ensembl_gene_id":"ENSG00000114315.3","gene_symbol":"HES1","gene_name":"hes family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:5192]","synonyms":"HRY,Hes1,HES-1,FLJ20408,bHLHb39","biotype":"protein_coding","ncbi_id":"3280","summary":"This protein belongs to the basic helix-loop-helix family of transcription factors. It is a transcriptional repressor of genes that require a bHLH protein for their transcription. The protein has a particular type of basic domain that contains a helix interrupting protein that binds to the N-box rather than the canonical E-box. [provided by RefSeq, Jul 2008]","start":194136145,"end":194138732,"strand":1,"description":"hes family bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:5192]"}, {"versioned_ensembl_gene_id":"ENSG00000229398.1","gene_symbol":"AL031667.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41382383,"end":41383107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234071.1","gene_symbol":"AC010099.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125344969,"end":125345377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255248.7","gene_symbol":"MIR100HG","gene_name":"mir-100-let-7a-2-mir-125b-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:39522]","synonyms":"linc-NeD125,AGD1,lncRNA-N2","biotype":"processed_transcript","ncbi_id":"399959","summary":"This gene produces long non-coding RNAs that act as regulators of cell proliferation. Alternative promoter usage and splicing results in multiple transcript variants. Some transcript variants may promote growth, while others may act to negatively regulate cell division. [provided by RefSeq, May 2016]","start":122028327,"end":122556721,"strand":-1,"description":"mir-100-let-7a-2-mir-125b-1 cluster host gene [Source:HGNC Symbol;Acc:HGNC:39522]"}, {"versioned_ensembl_gene_id":"ENSG00000083845.8","gene_symbol":"RPS5","gene_name":"ribosomal protein S5 [Source:HGNC Symbol;Acc:HGNC:10426]","synonyms":"S5","biotype":"protein_coding","ncbi_id":"6193","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S7P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":58386400,"end":58394806,"strand":1,"description":"ribosomal protein S5 [Source:HGNC Symbol;Acc:HGNC:10426]"}, {"versioned_ensembl_gene_id":"ENSG00000271681.1","gene_symbol":"AC136601.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178344843,"end":178345316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256723.1","gene_symbol":"AP003717.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73994972,"end":73996151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260100.1","gene_symbol":"AL512604.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37078813,"end":37079776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253608.1","gene_symbol":"AC022915.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48551567,"end":48698510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245688.1","gene_symbol":"AC008659.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":178438681,"end":178443094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266960.1","gene_symbol":"FAM106DP","gene_name":"family with sequence similarity 106 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:38397]","synonyms":"FAM106D","biotype":"unprocessed_pseudogene","ncbi_id":"100874406","summary":null,"start":60173322,"end":60173822,"strand":1,"description":"family with sequence similarity 106 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:38397]"}, {"versioned_ensembl_gene_id":"ENSG00000214457.3","gene_symbol":"RPL7P29","gene_name":"ribosomal protein L7 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35700]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643971","summary":null,"start":86970466,"end":86971193,"strand":1,"description":"ribosomal protein L7 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35700]"}, {"versioned_ensembl_gene_id":"ENSG00000088448.14","gene_symbol":"ANKRD10","gene_name":"ankyrin repeat domain 10 [Source:HGNC Symbol;Acc:HGNC:20265]","synonyms":"FLJ20093","biotype":"protein_coding","ncbi_id":"55608","summary":null,"start":110878540,"end":110915069,"strand":-1,"description":"ankyrin repeat domain 10 [Source:HGNC Symbol;Acc:HGNC:20265]"}, {"versioned_ensembl_gene_id":"ENSG00000159069.13","gene_symbol":"FBXW5","gene_name":"F-box and WD repeat domain containing 5 [Source:HGNC Symbol;Acc:HGNC:13613]","synonyms":"MGC20962,Fbw5,DKFZP434B205","biotype":"protein_coding","ncbi_id":"54461","summary":"This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into three classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene contains WD-40 domains, in addition to an F-box motif, so it belongs to the Fbw class. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene, however, they were found to be nonsense-mediated mRNA decay (NMD) candidates, hence not represented. [provided by RefSeq, Jul 2008]","start":136940435,"end":136944696,"strand":-1,"description":"F-box and WD repeat domain containing 5 [Source:HGNC Symbol;Acc:HGNC:13613]"}, {"versioned_ensembl_gene_id":"ENSG00000229921.6","gene_symbol":"KIF25-AS1","gene_name":"KIF25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20953]","synonyms":"NCRNA00300,HGC6.1.1,C6orf54","biotype":"lincRNA","ncbi_id":"100505879","summary":null,"start":167992822,"end":167997077,"strand":-1,"description":"KIF25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20953]"}, {"versioned_ensembl_gene_id":"ENSG00000125337.16","gene_symbol":"KIF25","gene_name":"kinesin family member 25 [Source:HGNC Symbol;Acc:HGNC:6390]","synonyms":"KNSL3","biotype":"protein_coding","ncbi_id":"3834","summary":"The protein encoded by this gene is a member of the kinesin-like protein family. Protein family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. However, the particular function of this gene product has not yet been determined. Two alternatively spliced transcript variants which encode products have been described. Other splice variants have been found that lack exon 2 and the initiation codon for translation. [provided by RefSeq, Jul 2008]","start":167996241,"end":168045089,"strand":1,"description":"kinesin family member 25 [Source:HGNC Symbol;Acc:HGNC:6390]"}, {"versioned_ensembl_gene_id":"ENSG00000137817.16","gene_symbol":"PARP6","gene_name":"poly(ADP-ribose) polymerase family member 6 [Source:HGNC Symbol;Acc:HGNC:26921]","synonyms":"pART17","biotype":"protein_coding","ncbi_id":"56965","summary":null,"start":72241181,"end":72272999,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 6 [Source:HGNC Symbol;Acc:HGNC:26921]"}, {"versioned_ensembl_gene_id":"ENSG00000186827.10","gene_symbol":"TNFRSF4","gene_name":"TNF receptor superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:11918]","synonyms":"TXGP1L,OX40,CD134,ACT35","biotype":"protein_coding","ncbi_id":"7293","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor has been shown to activate NF-kappaB through its interaction with adaptor proteins TRAF2 and TRAF5. Knockout studies in mice suggested that this receptor promotes the expression of apoptosis inhibitors BCL2 and BCL2lL1/BCL2-XL, and thus suppresses apoptosis. The knockout studies also suggested the roles of this receptor in CD4+ T cell response, as well as in T cell-dependent B cell proliferation and differentiation. [provided by RefSeq, Jul 2008]","start":1211326,"end":1214138,"strand":-1,"description":"TNF receptor superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:11918]"}, {"versioned_ensembl_gene_id":"ENSG00000253968.1","gene_symbol":"AC016573.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173414035,"end":173451165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255535.2","gene_symbol":"AP003041.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130040365,"end":130041071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081177.18","gene_symbol":"EXD2","gene_name":"exonuclease 3'-5' domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20217]","synonyms":"EXDL2,C14orf114,FLJ10738","biotype":"protein_coding","ncbi_id":"55218","summary":null,"start":69191511,"end":69244020,"strand":1,"description":"exonuclease 3'-5' domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20217]"}, {"versioned_ensembl_gene_id":"ENSG00000235994.4","gene_symbol":"AL049698.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":167975924,"end":167979776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089009.15","gene_symbol":"RPL6","gene_name":"ribosomal protein L6 [Source:HGNC Symbol;Acc:HGNC:10362]","synonyms":"TXREB1,TAXREB107,L6","biotype":"protein_coding","ncbi_id":"6128","summary":"This gene encodes a protein component of the 60S ribosomal subunit. This protein can bind specifically to domain C of the tax-responsive enhancer element of human T-cell leukemia virus type 1, and may participate in tax-mediated transactivation of transcription. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":112405190,"end":112418838,"strand":-1,"description":"ribosomal protein L6 [Source:HGNC Symbol;Acc:HGNC:10362]"}, {"versioned_ensembl_gene_id":"ENSG00000031081.10","gene_symbol":"ARHGAP31","gene_name":"Rho GTPase activating protein 31 [Source:HGNC Symbol;Acc:HGNC:29216]","synonyms":"CDGAP","biotype":"protein_coding","ncbi_id":"57514","summary":"This gene encodes a GTPase-activating protein (GAP). A variety of cellular processes are regulated by Rho GTPases which cycle between an inactive form bound to GDP and an active form bound to GTP. This cycling between inactive and active forms is regulated by guanine nucleotide exchange factors and GAPs. The encoded protein is a GAP shown to regulate two GTPases involved in protein trafficking and cell growth. [provided by RefSeq, Jul 2008]","start":119294373,"end":119420714,"strand":1,"description":"Rho GTPase activating protein 31 [Source:HGNC Symbol;Acc:HGNC:29216]"}, {"versioned_ensembl_gene_id":"ENSG00000100580.7","gene_symbol":"TMED8","gene_name":"transmembrane p24 trafficking protein family member 8 [Source:HGNC Symbol;Acc:HGNC:18633]","synonyms":"FAM15B","biotype":"protein_coding","ncbi_id":"283578","summary":null,"start":77335021,"end":77377109,"strand":-1,"description":"transmembrane p24 trafficking protein family member 8 [Source:HGNC Symbol;Acc:HGNC:18633]"}, {"versioned_ensembl_gene_id":"ENSG00000271522.1","gene_symbol":"AC016831.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130790208,"end":130791724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169926.10","gene_symbol":"KLF13","gene_name":"Kruppel like factor 13 [Source:HGNC Symbol;Acc:HGNC:13672]","synonyms":"BTEB3,RFLAT-1,NSLP1,FKLF-2,BTEB3,RFLAT-1,NSLP1,FKLF-2","biotype":"protein_coding","ncbi_id":"51621","summary":"KLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]","start":31326855,"end":31435665,"strand":1,"description":"Kruppel like factor 13 [Source:HGNC Symbol;Acc:HGNC:13672]"}, {"versioned_ensembl_gene_id":"ENSG00000091972.18","gene_symbol":"CD200","gene_name":"CD200 molecule [Source:HGNC Symbol;Acc:HGNC:7203]","synonyms":"MOX1,OX-2,MRC,MOX2","biotype":"protein_coding","ncbi_id":"4345","summary":"This gene encodes a type I membrane glycoprotein containing two extracellular immunoglobulin domains, a transmembrane and a cytoplasmic domain. This gene is expressed by various cell types, including B cells, a subset of T cells, thymocytes, endothelial cells, and neurons. The encoded protein plays an important role in immunosuppression and regulation of anti-tumor activity. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":112332347,"end":112362812,"strand":1,"description":"CD200 molecule [Source:HGNC Symbol;Acc:HGNC:7203]"}, {"versioned_ensembl_gene_id":"ENSG00000145911.5","gene_symbol":"N4BP3","gene_name":"NEDD4 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:29852]","synonyms":"LZTS4","biotype":"protein_coding","ncbi_id":"23138","summary":null,"start":178113443,"end":178126087,"strand":1,"description":"NEDD4 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:29852]"}, {"versioned_ensembl_gene_id":"ENSG00000231152.1","gene_symbol":"MTND2P15","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873346","summary":null,"start":69594041,"end":69594932,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42116]"}, {"versioned_ensembl_gene_id":"ENSG00000225499.1","gene_symbol":"AL663061.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31528114,"end":31528693,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168830.7","gene_symbol":"HTR1E","gene_name":"5-hydroxytryptamine receptor 1E [Source:HGNC Symbol;Acc:HGNC:5291]","synonyms":"5-HT1E","biotype":"protein_coding","ncbi_id":"3354","summary":null,"start":86937306,"end":87016683,"strand":1,"description":"5-hydroxytryptamine receptor 1E [Source:HGNC Symbol;Acc:HGNC:5291]"}, {"versioned_ensembl_gene_id":"ENSG00000266651.1","gene_symbol":"AC093484.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16440479,"end":16440952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248283.2","gene_symbol":"CCNL2P1","gene_name":"cyclin L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418743","summary":null,"start":42561457,"end":42562425,"strand":-1,"description":"cyclin L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50855]"}, {"versioned_ensembl_gene_id":"ENSG00000165623.9","gene_symbol":"UCMA","gene_name":"upper zone of growth plate and cartilage matrix associated [Source:HGNC Symbol;Acc:HGNC:25205]","synonyms":"C10orf49","biotype":"protein_coding","ncbi_id":"221044","summary":"This gene encodes a chondrocyte-specific, highly charged protein that is abundantly expressed in the upper immature zone of fetal and juvenile epiphyseal cartilage. The encoded protein undergoes proteolytic processing to generate a mature protein that is secreted into the extracellular matrix. The glutamic acid residues in the encoded protein undergo gamma carboxylation in a vitamin K-dependent manner. Undercarboxylation of the encoded protein is associated with osteoarthritis in humans. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2015]","start":13221767,"end":13234334,"strand":-1,"description":"upper zone of growth plate and cartilage matrix associated [Source:HGNC Symbol;Acc:HGNC:25205]"}, {"versioned_ensembl_gene_id":"ENSG00000006576.16","gene_symbol":"PHTF2","gene_name":"putative homeodomain transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:13411]","synonyms":"DKFZp434D166","biotype":"protein_coding","ncbi_id":"57157","summary":null,"start":77798792,"end":77957503,"strand":1,"description":"putative homeodomain transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:13411]"}, {"versioned_ensembl_gene_id":"ENSG00000263293.2","gene_symbol":"THCAT158","gene_name":"thyroid cancer-associated transcript 158 [Source:NCBI gene;Acc:102724508]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724508","summary":null,"start":47303460,"end":47323613,"strand":-1,"description":"thyroid cancer-associated transcript 158 [Source:NCBI gene;Acc:102724508]"}, {"versioned_ensembl_gene_id":"ENSG00000186628.12","gene_symbol":"FSD2","gene_name":"fibronectin type III and SPRY domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18024]","synonyms":"SPRYD1,RP11-127F21","biotype":"protein_coding","ncbi_id":"123722","summary":"This gene encodes a protein that belongs to the FN3/SPRY family of proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":82755362,"end":82806070,"strand":-1,"description":"fibronectin type III and SPRY domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18024]"}, {"versioned_ensembl_gene_id":"ENSG00000198131.13","gene_symbol":"ZNF544","gene_name":"zinc finger protein 544 [Source:HGNC Symbol;Acc:HGNC:16759]","synonyms":"AF020591","biotype":"protein_coding","ncbi_id":"27300","summary":null,"start":58228594,"end":58277495,"strand":1,"description":"zinc finger protein 544 [Source:HGNC Symbol;Acc:HGNC:16759]"}, {"versioned_ensembl_gene_id":"ENSG00000234448.1","gene_symbol":"AL606490.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48371905,"end":48372095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196199.13","gene_symbol":"MPHOSPH8","gene_name":"M-phase phosphoprotein 8 [Source:HGNC Symbol;Acc:HGNC:29810]","synonyms":"mpp8,HSMPP8","biotype":"protein_coding","ncbi_id":"54737","summary":null,"start":19633681,"end":19673459,"strand":1,"description":"M-phase phosphoprotein 8 [Source:HGNC Symbol;Acc:HGNC:29810]"}, {"versioned_ensembl_gene_id":"ENSG00000228141.7","gene_symbol":"AC105339.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":82710471,"end":82714029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270071.1","gene_symbol":"AP001172.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16291791,"end":16308133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138109.9","gene_symbol":"CYP2C9","gene_name":"cytochrome P450 family 2 subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:2623]","synonyms":"CYP2C10,P450IIC9","biotype":"protein_coding","ncbi_id":"1559","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by rifampin. The enzyme is known to metabolize many xenobiotics, including phenytoin, tolbutamide, ibuprofen and S-warfarin. Studies identifying individuals who are poor metabolizers of phenytoin and tolbutamide suggest that this gene is polymorphic. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. [provided by RefSeq, Jul 2008]","start":94938658,"end":94989390,"strand":1,"description":"cytochrome P450 family 2 subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:2623]"}, {"versioned_ensembl_gene_id":"ENSG00000258763.5","gene_symbol":"AC122685.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55434734,"end":55585471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228369.2","gene_symbol":"TXNDC12-AS1","gene_name":"TXNDC12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30008]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355143","summary":null,"start":52050918,"end":52052683,"strand":1,"description":"TXNDC12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30008]"}, {"versioned_ensembl_gene_id":"ENSG00000226084.5","gene_symbol":"AC113935.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77129114,"end":77129668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110911.14","gene_symbol":"SLC11A2","gene_name":"solute carrier family 11 member 2 [Source:HGNC Symbol;Acc:HGNC:10908]","synonyms":"NRAMP2,DMT1,DCT1","biotype":"protein_coding","ncbi_id":"4891","summary":"This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]","start":50979401,"end":51028566,"strand":-1,"description":"solute carrier family 11 member 2 [Source:HGNC Symbol;Acc:HGNC:10908]"}, {"versioned_ensembl_gene_id":"ENSG00000167770.11","gene_symbol":"OTUB1","gene_name":"OTU deubiquitinase, ubiquitin aldehyde binding 1 [Source:HGNC Symbol;Acc:HGNC:23077]","synonyms":"FLJ40710,FLJ20113","biotype":"protein_coding","ncbi_id":"55611","summary":"The product of this gene is a member of the OTU (ovarian tumor) superfamily of predicted cysteine proteases. The encoded protein is a highly specific ubiquitin iso-peptidase, and cleaves ubiquitin from branched poly-ubiquitin chains but not from ubiquitinated substrates. It interacts with another ubiquitin protease and an E3 ubiquitin ligase that inhibits cytokine gene transcription in the immune system. It is proposed to function in specific ubiquitin-dependent pathways, possibly by providing an editing function for polyubiquitin chain growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":63985853,"end":64001811,"strand":1,"description":"OTU deubiquitinase, ubiquitin aldehyde binding 1 [Source:HGNC Symbol;Acc:HGNC:23077]"}, {"versioned_ensembl_gene_id":"ENSG00000100968.13","gene_symbol":"NFATC4","gene_name":"nuclear factor of activated T-cells 4 [Source:HGNC Symbol;Acc:HGNC:7778]","synonyms":"NFAT3","biotype":"protein_coding","ncbi_id":"4776","summary":"This gene encodes a member of the nuclear factor of activated T cells (NFAT) protein family. The encoded protein is part of a DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor stimulation and an inducible nuclear component. NFAT proteins are activated by the calmodulin-dependent phosphatase, calcineurin. The encoded protein plays a role in the inducible expression of cytokine genes in T cells, especially in the induction of interleukin-2 and interleukin-4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":24365673,"end":24379604,"strand":1,"description":"nuclear factor of activated T-cells 4 [Source:HGNC Symbol;Acc:HGNC:7778]"}, {"versioned_ensembl_gene_id":"ENSG00000133315.10","gene_symbol":"MACROD1","gene_name":"MACRO domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29598]","synonyms":"LRP16","biotype":"protein_coding","ncbi_id":"28992","summary":null,"start":63998558,"end":64166106,"strand":-1,"description":"MACRO domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29598]"}, {"versioned_ensembl_gene_id":"ENSG00000266901.1","gene_symbol":"AC068473.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79702721,"end":79703651,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259514.1","gene_symbol":"AC027243.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76339609,"end":76342063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271659.1","gene_symbol":"AL161729.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95514045,"end":95514520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256824.1","gene_symbol":"AP000721.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64035970,"end":64103653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268293.1","gene_symbol":"AC008751.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58136713,"end":58137054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010404.17","gene_symbol":"IDS","gene_name":"iduronate 2-sulfatase [Source:HGNC Symbol;Acc:HGNC:5389]","synonyms":"SIDS","biotype":"protein_coding","ncbi_id":"3423","summary":"This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":149476990,"end":149521096,"strand":-1,"description":"iduronate 2-sulfatase [Source:HGNC Symbol;Acc:HGNC:5389]"}, {"versioned_ensembl_gene_id":"ENSG00000006695.10","gene_symbol":"COX10","gene_name":"COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:2260]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1352","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion. [provided by RefSeq, Jul 2008]","start":14069496,"end":14208677,"strand":1,"description":"COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:2260]"}, {"versioned_ensembl_gene_id":"ENSG00000241489.7","gene_symbol":"AC244197.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":149482543,"end":149533935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232851.3","gene_symbol":"ATP5J2P3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21286]","synonyms":"bA159H20.5","biotype":"processed_pseudogene","ncbi_id":"445573","summary":null,"start":77040416,"end":77040673,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21286]"}, {"versioned_ensembl_gene_id":"ENSG00000170448.11","gene_symbol":"NFXL1","gene_name":"nuclear transcription factor, X-box binding like 1 [Source:HGNC Symbol;Acc:HGNC:18726]","synonyms":"HOZFP","biotype":"protein_coding","ncbi_id":"152518","summary":null,"start":47847233,"end":47914667,"strand":-1,"description":"nuclear transcription factor, X-box binding like 1 [Source:HGNC Symbol;Acc:HGNC:18726]"}, {"versioned_ensembl_gene_id":"ENSG00000225926.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29897284,"end":29897650,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000117868.15","gene_symbol":"ESYT2","gene_name":"extended synaptotagmin 2 [Source:HGNC Symbol;Acc:HGNC:22211]","synonyms":"KIAA1228,FAM62B,CHR2SYT","biotype":"protein_coding","ncbi_id":"57488","summary":null,"start":158730995,"end":158830253,"strand":-1,"description":"extended synaptotagmin 2 [Source:HGNC Symbol;Acc:HGNC:22211]"}, {"versioned_ensembl_gene_id":"ENSG00000050820.16","gene_symbol":"BCAR1","gene_name":"BCAR1, Cas family scaffolding protein [Source:HGNC Symbol;Acc:HGNC:971]","synonyms":"P130Cas,Crkas,CASS1,CAS","biotype":"protein_coding","ncbi_id":"9564","summary":"The protein encoded by this gene is a member of the Crk-associated substrate (CAS) family of scaffold proteins, characterized by the presence of multiple protein-protein interaction domains and many serine and tyrosine phosphorylation sites. The encoded protein contains a Src-homology 3 (SH3) domain, a proline-rich domain, a substrate domain which contains 15 repeat of the YxxP consensus phosphorylation motif for Src family kinases, a serine-rich domain, and a bipartite Src-binding domain, which can bind both SH2 and SH3 domains. This adaptor protein functions in multiple cellular pathways, including in cell motility, apoptosis and cell cycle control. Dysregulation of this gene can have a wide range of effects, affecting different pathways, including cardiac development, vascular smooth muscle cells, liver and kidney function, endothelial migration, and cancer. [provided by RefSeq, Sep 2017]","start":75228187,"end":75268053,"strand":-1,"description":"BCAR1, Cas family scaffolding protein [Source:HGNC Symbol;Acc:HGNC:971]"}, {"versioned_ensembl_gene_id":"ENSG00000120500.17","gene_symbol":"ARR3","gene_name":"arrestin 3 [Source:HGNC Symbol;Acc:HGNC:710]","synonyms":"ARRX","biotype":"protein_coding","ncbi_id":"407","summary":"The protein encoded by this gene is a non-visual arrestin which binds to agonist-activated, phosphorylated G protein-coupled receptors. This binding uncouples the receptor from the heterotrimeric G protein, resulting in termination of the G protein-coupled receptor signaling. The encoded protein also is a part of the centrosome, interacting with gamma-tubulin to help regulate proper centrosome function. [provided by RefSeq, May 2016]","start":70268305,"end":70281840,"strand":1,"description":"arrestin 3 [Source:HGNC Symbol;Acc:HGNC:710]"}, {"versioned_ensembl_gene_id":"ENSG00000280152.1","gene_symbol":"AC009078.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75245994,"end":75250077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213185.6","gene_symbol":"FAM24B","gene_name":"family with sequence similarity 24 member B [Source:HGNC Symbol;Acc:HGNC:23475]","synonyms":"MGC45962,AC073585.2","biotype":"protein_coding","ncbi_id":"196792","summary":null,"start":122849078,"end":122879641,"strand":-1,"description":"family with sequence similarity 24 member B [Source:HGNC Symbol;Acc:HGNC:23475]"}, {"versioned_ensembl_gene_id":"ENSG00000157800.17","gene_symbol":"SLC37A3","gene_name":"solute carrier family 37 member 3 [Source:HGNC Symbol;Acc:HGNC:20651]","synonyms":"DKFZp761N0624","biotype":"protein_coding","ncbi_id":"84255","summary":null,"start":140293693,"end":140404433,"strand":-1,"description":"solute carrier family 37 member 3 [Source:HGNC Symbol;Acc:HGNC:20651]"}, {"versioned_ensembl_gene_id":"ENSG00000232768.1","gene_symbol":"AL356320.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31050872,"end":31051034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231912.2","gene_symbol":"FO393415.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113791829,"end":113837368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219758.6","gene_symbol":"FO393415.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113839279,"end":113839621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271752.1","gene_symbol":"AC112187.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50662859,"end":50663266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282364.1","gene_symbol":"AC004980.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76638217,"end":76638713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230943.1","gene_symbol":"LINC02541","gene_name":"long intergenic non-protein coding RNA 2541 [Source:HGNC Symbol;Acc:HGNC:53574]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927686","summary":null,"start":113623535,"end":113650074,"strand":-1,"description":"long intergenic non-protein coding RNA 2541 [Source:HGNC Symbol;Acc:HGNC:53574]"}, {"versioned_ensembl_gene_id":"ENSG00000236154.1","gene_symbol":"AL450311.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69575807,"end":69577154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187969.5","gene_symbol":"ZCCHC13","gene_name":"zinc finger CCHC-type containing 13 [Source:HGNC Symbol;Acc:HGNC:31749]","synonyms":"ZNF9L,Cnbp2,4930513O09RIK","biotype":"protein_coding","ncbi_id":"389874","summary":"This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 3. However, the CDS of this intronless gene remains relatively intact, it is conserved in other mammalian species, it is known to be transcribed, and it is therefore thought to encode a functional protein. The encoded protein contains six CCHC-type zinc fingers, and is thus thought to function as a transcription factor. [provided by RefSeq, May 2010]","start":74304190,"end":74305031,"strand":1,"description":"zinc finger CCHC-type containing 13 [Source:HGNC Symbol;Acc:HGNC:31749]"}, {"versioned_ensembl_gene_id":"ENSG00000256372.1","gene_symbol":"AC023050.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31853021,"end":31853407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188375.4","gene_symbol":"H3F3C","gene_name":"H3 histone family member 3C [Source:HGNC Symbol;Acc:HGNC:33164]","synonyms":"H3.5","biotype":"protein_coding","ncbi_id":"440093","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene contains introns and its mRNA is polyadenylated, unlike most histone genes. The protein encoded by this gene is a replication-independent histone that is a member of the histone H3 family. [provided by RefSeq, Oct 2015]","start":31791185,"end":31792241,"strand":-1,"description":"H3 histone family member 3C [Source:HGNC Symbol;Acc:HGNC:33164]"}, {"versioned_ensembl_gene_id":"ENSG00000226092.4","gene_symbol":"RBMY2AP","gene_name":"RNA binding motif protein, Y-linked, family 2, member A pseudogene [Source:HGNC Symbol;Acc:HGNC:9917]","synonyms":"RBMY2A","biotype":"unprocessed_pseudogene","ncbi_id":"5945","summary":null,"start":21927521,"end":21937150,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member A pseudogene [Source:HGNC Symbol;Acc:HGNC:9917]"}, {"versioned_ensembl_gene_id":"ENSG00000100150.16","gene_symbol":"DEPDC5","gene_name":"DEP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:18423]","synonyms":"KIAA0645,DEP.5","biotype":"protein_coding","ncbi_id":"9681","summary":"This gene encodes a member of the IML1 family of proteins involved in G-protein signaling pathways. The mechanistic target of rapamycin complex 1 (mTORC1) pathway regulates cell growth by sensing the availability of nutrients. The protein encoded by this gene is a component of the GATOR1 (GAP activity toward Rags) complex which inhibits the amino acid-sensing branch of the mTORC1 pathway. Mutations in this gene are associated with autosomal dominant familial focal epilepsy with variable foci. A single nucleotide polymorphism in an intron of this gene has been associated with an increased risk of hepatocellular carcinoma in individuals with chronic hepatitis C virus infection. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":31753951,"end":31907034,"strand":1,"description":"DEP domain containing 5 [Source:HGNC Symbol;Acc:HGNC:18423]"}, {"versioned_ensembl_gene_id":"ENSG00000255992.1","gene_symbol":"AC131009.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131924736,"end":131929351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273568.1","gene_symbol":"AC131009.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":131934642,"end":131934928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145354.9","gene_symbol":"CISD2","gene_name":"CDGSH iron sulfur domain 2 [Source:HGNC Symbol;Acc:HGNC:24212]","synonyms":"ZCD2,WFS2,NAF-1,Miner1,ERIS","biotype":"protein_coding","ncbi_id":"493856","summary":"The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2. [provided by RefSeq, Mar 2011]","start":102868978,"end":102889242,"strand":1,"description":"CDGSH iron sulfur domain 2 [Source:HGNC Symbol;Acc:HGNC:24212]"}, {"versioned_ensembl_gene_id":"ENSG00000246790.2","gene_symbol":"AP000977.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121447331,"end":121453013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253218.1","gene_symbol":"KLF3P1","gene_name":"Kruppel like factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651815","summary":null,"start":172254418,"end":172255439,"strand":-1,"description":"Kruppel like factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41518]"}, {"versioned_ensembl_gene_id":"ENSG00000187210.12","gene_symbol":"GCNT1","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 [Source:HGNC Symbol;Acc:HGNC:4203]","synonyms":"NAGCT2,NACGT2,C2GNT","biotype":"protein_coding","ncbi_id":"2650","summary":"This gene is a member of the beta-1,6-N-acetylglucosaminyltransferase gene family. It is essential to the formation of Gal beta 1-3(GlcNAc beta 1-6)GalNAc structures and the core 2 O-glycan branch. The gene coding this enzyme was originally mapped to 9q21, but was later localized to 9q13. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":76419850,"end":76507416,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 [Source:HGNC Symbol;Acc:HGNC:4203]"}, {"versioned_ensembl_gene_id":"ENSG00000235568.6","gene_symbol":"NFAM1","gene_name":"NFAT activating protein with ITAM motif 1 [Source:HGNC Symbol;Acc:HGNC:29872]","synonyms":"CNAIP","biotype":"protein_coding","ncbi_id":"150372","summary":"The protein encoded by this gene is a type I membrane receptor that activates cytokine gene promoters such as the IL-13 and TNF-alpha promoters. The encoded protein contains an immunoreceptor tyrosine-based activation motif (ITAM) and is thought to regulate the signaling and development of B-cells. [provided by RefSeq, Jul 2008]","start":42380410,"end":42432395,"strand":-1,"description":"NFAT activating protein with ITAM motif 1 [Source:HGNC Symbol;Acc:HGNC:29872]"}, {"versioned_ensembl_gene_id":"ENSG00000026025.15","gene_symbol":"VIM","gene_name":"vimentin [Source:HGNC Symbol;Acc:HGNC:12692]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7431","summary":"This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017]","start":17228259,"end":17237593,"strand":1,"description":"vimentin [Source:HGNC Symbol;Acc:HGNC:12692]"}, {"versioned_ensembl_gene_id":"ENSG00000279198.1","gene_symbol":"AC008894.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16074293,"end":16077395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073578.16","gene_symbol":"SDHA","gene_name":"succinate dehydrogenase complex flavoprotein subunit A [Source:HGNC Symbol;Acc:HGNC:10680]","synonyms":"SDHF,SDH2,FP","biotype":"protein_coding","ncbi_id":"6389","summary":"This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":218241,"end":256700,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A [Source:HGNC Symbol;Acc:HGNC:10680]"}, {"versioned_ensembl_gene_id":"ENSG00000109184.14","gene_symbol":"DCUN1D4","gene_name":"defective in cullin neddylation 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28998]","synonyms":"KIAA0276","biotype":"protein_coding","ncbi_id":"23142","summary":null,"start":51843000,"end":51916837,"strand":1,"description":"defective in cullin neddylation 1 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28998]"}, {"versioned_ensembl_gene_id":"ENSG00000104177.17","gene_symbol":"MYEF2","gene_name":"myelin expression factor 2 [Source:HGNC Symbol;Acc:HGNC:17940]","synonyms":"MEF-2,KIAA1341,HsT18564,FLJ11213","biotype":"protein_coding","ncbi_id":"50804","summary":null,"start":48134631,"end":48178517,"strand":-1,"description":"myelin expression factor 2 [Source:HGNC Symbol;Acc:HGNC:17940]"}, {"versioned_ensembl_gene_id":"ENSG00000198703.2","gene_symbol":"OR10R3P","gene_name":"olfactory receptor family 10 subfamily R member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14829]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391110","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158491219,"end":158492160,"strand":1,"description":"olfactory receptor family 10 subfamily R member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:14829]"}, {"versioned_ensembl_gene_id":"ENSG00000258599.2","gene_symbol":"AL355922.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20983155,"end":20985066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060749.14","gene_symbol":"QSER1","gene_name":"glutamine and serine rich 1 [Source:HGNC Symbol;Acc:HGNC:26154]","synonyms":"FLJ21924","biotype":"protein_coding","ncbi_id":"79832","summary":null,"start":32893178,"end":32993316,"strand":1,"description":"glutamine and serine rich 1 [Source:HGNC Symbol;Acc:HGNC:26154]"}, {"versioned_ensembl_gene_id":"ENSG00000255297.1","gene_symbol":"OR4A41P","gene_name":"olfactory receptor family 4 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31260]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403247","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48589760,"end":48590687,"strand":1,"description":"olfactory receptor family 4 subfamily A member 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:31260]"}, {"versioned_ensembl_gene_id":"ENSG00000198833.6","gene_symbol":"UBE2J1","gene_name":"ubiquitin conjugating enzyme E2 J1 [Source:HGNC Symbol;Acc:HGNC:17598]","synonyms":"UBC6,NCUBE1,HSPC153,CGI-76","biotype":"protein_coding","ncbi_id":"51465","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is located in the membrane of the endoplasmic reticulum (ER) and may contribute to quality control ER-associated degradation by the ubiquitin-proteasome system. [provided by RefSeq, Jul 2008]","start":89326625,"end":89352848,"strand":-1,"description":"ubiquitin conjugating enzyme E2 J1 [Source:HGNC Symbol;Acc:HGNC:17598]"}, {"versioned_ensembl_gene_id":"ENSG00000203588.3","gene_symbol":"IGBP1-AS1","gene_name":"IGBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40295]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873991","summary":null,"start":70163842,"end":70165206,"strand":-1,"description":"IGBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40295]"}, {"versioned_ensembl_gene_id":"ENSG00000259948.2","gene_symbol":"AC124068.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89201091,"end":89201768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281756.1","gene_symbol":"C2-AS1","gene_name":"C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49464]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102060414","summary":null,"start":31934474,"end":31941724,"strand":-1,"description":"C2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49464]"}, {"versioned_ensembl_gene_id":"ENSG00000162521.18","gene_symbol":"RBBP4","gene_name":"RB binding protein 4, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:9887]","synonyms":"RbAp48,NURF55,lin-53","biotype":"protein_coding","ncbi_id":"5928","summary":"This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. It is present in protein complexes involved in histone acetylation and chromatin assembly. It is part of the Mi-2 complex which has been implicated in chromatin remodeling and transcriptional repression associated with histone deacetylation. This encoded protein is also part of co-repressor complexes, which is an integral component of transcriptional silencing. It is found among several cellular proteins that bind directly to retinoblastoma protein to regulate cell proliferation. This protein also seems to be involved in transcriptional repression of E2F-responsive genes. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":32651142,"end":32686211,"strand":1,"description":"RB binding protein 4, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:9887]"}, {"versioned_ensembl_gene_id":"ENSG00000165280.15","gene_symbol":"VCP","gene_name":"valosin containing protein [Source:HGNC Symbol;Acc:HGNC:12666]","synonyms":"p97,IBMPFD,CDC48","biotype":"protein_coding","ncbi_id":"7415","summary":"This gene encodes a member of the AAA ATPase family of proteins. The encoded protein plays a role in protein degradation, intracellular membrane fusion, DNA repair and replication, regulation of the cell cycle, and activation of the NF-kappa B pathway. This protein forms a homohexameric complex that interacts with a variety of cofactors and extracts ubiquitinated proteins from lipid membranes or protein complexes. Mutations in this gene cause IBMPFD (inclusion body myopathy with paget disease of bone and frontotemporal dementia), ALS (amyotrophic lateral sclerosis) and Charcot-Marie-Tooth disease in human patients. [provided by RefSeq, Aug 2017]","start":35056064,"end":35073249,"strand":-1,"description":"valosin containing protein [Source:HGNC Symbol;Acc:HGNC:12666]"}, {"versioned_ensembl_gene_id":"ENSG00000114529.12","gene_symbol":"C3orf52","gene_name":"chromosome 3 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:26255]","synonyms":"TTMP,FLJ23186","biotype":"protein_coding","ncbi_id":"79669","summary":null,"start":112086335,"end":112131004,"strand":1,"description":"chromosome 3 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:26255]"}, {"versioned_ensembl_gene_id":"ENSG00000232827.2","gene_symbol":"LINC01189","gene_name":"long intergenic non-protein coding RNA 1189 [Source:HGNC Symbol;Acc:HGNC:49592]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643648","summary":null,"start":62515191,"end":62522018,"strand":1,"description":"long intergenic non-protein coding RNA 1189 [Source:HGNC Symbol;Acc:HGNC:49592]"}, {"versioned_ensembl_gene_id":"ENSG00000232572.1","gene_symbol":"BX001040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31518383,"end":31518962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233699.1","gene_symbol":"TTTY18","gene_name":"testis-specific transcript, Y-linked 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18842]","synonyms":"NCRNA00143","biotype":"lincRNA","ncbi_id":"252950","summary":null,"start":8683370,"end":8683878,"strand":-1,"description":"testis-specific transcript, Y-linked 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18842]"}, {"versioned_ensembl_gene_id":"ENSG00000228127.2","gene_symbol":"LINC01649","gene_name":"long intergenic non-protein coding RNA 1649 [Source:HGNC Symbol;Acc:HGNC:52436]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928995","summary":null,"start":115919350,"end":115931561,"strand":1,"description":"long intergenic non-protein coding RNA 1649 [Source:HGNC Symbol;Acc:HGNC:52436]"}, {"versioned_ensembl_gene_id":"ENSG00000277766.1","gene_symbol":"AC004790.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16037009,"end":16038455,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275210.1","gene_symbol":"AC245884.11","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54308915,"end":54337168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224908.1","gene_symbol":"TIMM8BP2","gene_name":"translocase of inner mitochondrial membrane 8B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39212]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874417","summary":null,"start":134166682,"end":134166932,"strand":1,"description":"translocase of inner mitochondrial membrane 8B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39212]"}, {"versioned_ensembl_gene_id":"ENSG00000280865.1","gene_symbol":"AC233280.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144306.14","gene_symbol":"SCRN3","gene_name":"secernin 3 [Source:HGNC Symbol;Acc:HGNC:30382]","synonyms":"FLJ23142","biotype":"protein_coding","ncbi_id":"79634","summary":null,"start":174395730,"end":174429575,"strand":1,"description":"secernin 3 [Source:HGNC Symbol;Acc:HGNC:30382]"}, {"versioned_ensembl_gene_id":"ENSG00000085978.21","gene_symbol":"ATG16L1","gene_name":"autophagy related 16 like 1 [Source:HGNC Symbol;Acc:HGNC:21498]","synonyms":"APG16L,WDR30,FLJ10035,ATG16L,ATG16A","biotype":"protein_coding","ncbi_id":"55054","summary":"The protein encoded by this gene is part of a large protein complex that is necessary for autophagy, the major process by which intracellular components are targeted to lysosomes for degradation. Defects in this gene are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]","start":233210051,"end":233295674,"strand":1,"description":"autophagy related 16 like 1 [Source:HGNC Symbol;Acc:HGNC:21498]"}, {"versioned_ensembl_gene_id":"ENSG00000100207.18","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42160013,"end":42343616,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000284600.1","gene_symbol":"AC093390.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1795525,"end":1811526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273553.1","gene_symbol":"AC016597.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27687182,"end":27687522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000057935.13","gene_symbol":"MTA3","gene_name":"metastasis associated 1 family member 3 [Source:HGNC Symbol;Acc:HGNC:23784]","synonyms":"KIAA1266","biotype":"protein_coding","ncbi_id":"57504","summary":null,"start":42494569,"end":42756947,"strand":1,"description":"metastasis associated 1 family member 3 [Source:HGNC Symbol;Acc:HGNC:23784]"}, {"versioned_ensembl_gene_id":"ENSG00000171722.12","gene_symbol":"SPATA46","gene_name":"spermatogenesis associated 46 [Source:HGNC Symbol;Acc:HGNC:27648]","synonyms":"C1orf111","biotype":"protein_coding","ncbi_id":"284680","summary":null,"start":162373203,"end":162376870,"strand":-1,"description":"spermatogenesis associated 46 [Source:HGNC Symbol;Acc:HGNC:27648]"}, {"versioned_ensembl_gene_id":"ENSG00000253102.1","gene_symbol":"AC004707.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50396438,"end":50397888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230409.3","gene_symbol":"TCEA1P2","gene_name":"transcription elongation factor A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29891]","synonyms":"TCEA1","biotype":"processed_pseudogene","ncbi_id":"399511","summary":null,"start":37275693,"end":37276598,"strand":1,"description":"transcription elongation factor A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29891]"}, {"versioned_ensembl_gene_id":"ENSG00000229526.2","gene_symbol":"KRT16P4","gene_name":"keratin 16 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37809]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"339244","summary":null,"start":18450244,"end":18475920,"strand":1,"description":"keratin 16 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37809]"}, {"versioned_ensembl_gene_id":"ENSG00000198929.12","gene_symbol":"NOS1AP","gene_name":"nitric oxide synthase 1 adaptor protein [Source:HGNC Symbol;Acc:HGNC:16859]","synonyms":"KIAA0464,CAPON","biotype":"protein_coding","ncbi_id":"9722","summary":"This gene encodes a cytosolic protein that binds to the signaling molecule, neuronal nitric oxide synthase (nNOS). This protein has a C-terminal PDZ-binding domain that mediates interactions with nNOS and an N-terminal phosphotyrosine binding (PTB) domain that binds to the small monomeric G protein, Dexras1. Studies of the related mouse and rat proteins have shown that this protein functions as an adapter protein linking nNOS to specific targets, such as Dexras1 and the synapsins. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2009]","start":162069774,"end":162370475,"strand":1,"description":"nitric oxide synthase 1 adaptor protein [Source:HGNC Symbol;Acc:HGNC:16859]"}, {"versioned_ensembl_gene_id":"ENSG00000139344.7","gene_symbol":"AMDHD1","gene_name":"amidohydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28577]","synonyms":"MGC35366","biotype":"protein_coding","ncbi_id":"144193","summary":null,"start":95943293,"end":95968716,"strand":1,"description":"amidohydrolase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28577]"}, {"versioned_ensembl_gene_id":"ENSG00000215375.6","gene_symbol":"MYL5","gene_name":"myosin light chain 5 [Source:HGNC Symbol;Acc:HGNC:7586]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4636","summary":"This gene encodes one of the myosin light chains, a component of the hexameric ATPase cellular motor protein myosin. Myosin is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene product, one of the regulatory light chains, is expressed in fetal muscle and in adult retina, cerebellum, and basal ganglia. [provided by RefSeq, Jul 2008]","start":673580,"end":682033,"strand":1,"description":"myosin light chain 5 [Source:HGNC Symbol;Acc:HGNC:7586]"}, {"versioned_ensembl_gene_id":"ENSG00000254335.1","gene_symbol":"CDH12P1","gene_name":"cadherin 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37698]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100093625","summary":null,"start":70860285,"end":70860579,"strand":-1,"description":"cadherin 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37698]"}, {"versioned_ensembl_gene_id":"ENSG00000226609.1","gene_symbol":"AL390067.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112748902,"end":112750456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177302.14","gene_symbol":"TOP3A","gene_name":"topoisomerase (DNA) III alpha [Source:HGNC Symbol;Acc:HGNC:11992]","synonyms":"ZGRF7,TOP3","biotype":"protein_coding","ncbi_id":"7156","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus reducing the number of supercoils and altering the topology of DNA. This enzyme forms a complex with BLM which functions in the regulation of recombination in somatic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":18271428,"end":18315007,"strand":-1,"description":"topoisomerase (DNA) III alpha [Source:HGNC Symbol;Acc:HGNC:11992]"}, {"versioned_ensembl_gene_id":"ENSG00000228000.1","gene_symbol":"AC127537.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18311904,"end":18312651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005194.14","gene_symbol":"CIAPIN1","gene_name":"cytokine induced apoptosis inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28050]","synonyms":"Anamorsin","biotype":"protein_coding","ncbi_id":"57019","summary":"CIAPIN1 is a cytokine-induced inhibitor of apoptosis with no relation to apoptosis regulatory molecules of the BCL2 (MIM 151430) or CASP (see MIM 147678) families. Expression of CIAPIN1 is dependent on growth factor stimulation (Shibayama et al., 2004 [PubMed 14970183]).[supplied by OMIM, Mar 2008]","start":57428169,"end":57447528,"strand":-1,"description":"cytokine induced apoptosis inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28050]"}, {"versioned_ensembl_gene_id":"ENSG00000260379.1","gene_symbol":"AC074052.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8508069,"end":8508585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236565.3","gene_symbol":"HNRNPA3P5","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387933","summary":null,"start":65787932,"end":65788764,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39774]"}, {"versioned_ensembl_gene_id":"ENSG00000229265.1","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"D84394.7,USP8P,KIAA0055-hom","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31318990,"end":31322162,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000248417.1","gene_symbol":"AC097535.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33433510,"end":33437877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267233.1","gene_symbol":"HNRNPA3P16","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:48762]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421451","summary":null,"start":50814392,"end":50815730,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:48762]"}, {"versioned_ensembl_gene_id":"ENSG00000166840.13","gene_symbol":"GLYATL1","gene_name":"glycine-N-acyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:30519]","synonyms":"MGC15397,FLJ34646","biotype":"protein_coding","ncbi_id":"92292","summary":null,"start":58905398,"end":59043527,"strand":1,"description":"glycine-N-acyltransferase like 1 [Source:HGNC Symbol;Acc:HGNC:30519]"}, {"versioned_ensembl_gene_id":"ENSG00000260289.1","gene_symbol":"AC093515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7888489,"end":7894395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223724.1","gene_symbol":"RAD17P2","gene_name":"RAD17 checkpoint clamp loader component pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9809]","synonyms":"HRAD17P2","biotype":"processed_pseudogene","ncbi_id":"9206","summary":null,"start":49044079,"end":49046794,"strand":-1,"description":"RAD17 checkpoint clamp loader component pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9809]"}, {"versioned_ensembl_gene_id":"ENSG00000162923.14","gene_symbol":"WDR26","gene_name":"WD repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:21208]","synonyms":"GID7,FLJ21016","biotype":"protein_coding","ncbi_id":"80232","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":224385143,"end":224437033,"strand":-1,"description":"WD repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:21208]"}, {"versioned_ensembl_gene_id":"ENSG00000279107.1","gene_symbol":"AC138951.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21493436,"end":21494596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267392.3","gene_symbol":"CYP4F9P","gene_name":"cytochrome P450 family 4 subfamily F member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:39940]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100506916","summary":null,"start":15979835,"end":15999020,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:39940]"}, {"versioned_ensembl_gene_id":"ENSG00000279104.1","gene_symbol":"AC093775.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49760897,"end":49762764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269983.1","gene_symbol":"AC146944.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70449636,"end":70450353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271931.1","gene_symbol":"AL353135.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89080164,"end":89080667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248308.1","gene_symbol":"AC138938.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20830166,"end":20830947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106785.14","gene_symbol":"TRIM14","gene_name":"tripartite motif containing 14 [Source:HGNC Symbol;Acc:HGNC:16283]","synonyms":"KIAA0129","biotype":"protein_coding","ncbi_id":"9830","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies and its function has not been determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":98069275,"end":98119212,"strand":-1,"description":"tripartite motif containing 14 [Source:HGNC Symbol;Acc:HGNC:16283]"}, {"versioned_ensembl_gene_id":"ENSG00000260236.1","gene_symbol":"AC099778.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47379089,"end":47380999,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255265.1","gene_symbol":"TMA16P1","gene_name":"translation machinery associated 16 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101405","summary":null,"start":58796237,"end":58796854,"strand":-1,"description":"translation machinery associated 16 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43780]"}, {"versioned_ensembl_gene_id":"ENSG00000228264.1","gene_symbol":"PSMD8P1","gene_name":"proteasome 26S subunit, non-ATPase, 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422411","summary":null,"start":154414369,"end":154415137,"strand":-1,"description":"proteasome 26S subunit, non-ATPase, 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34013]"}, {"versioned_ensembl_gene_id":"ENSG00000277463.1","gene_symbol":"AC080038.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62626031,"end":62626453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176547.9","gene_symbol":"OR4C3","gene_name":"olfactory receptor family 4 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:14697]","synonyms":null,"biotype":"protein_coding","ncbi_id":"256144","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48324920,"end":48328471,"strand":1,"description":"olfactory receptor family 4 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:14697]"}, {"versioned_ensembl_gene_id":"ENSG00000052749.13","gene_symbol":"RRP12","gene_name":"ribosomal RNA processing 12 homolog [Source:HGNC Symbol;Acc:HGNC:29100]","synonyms":"KIAA0690","biotype":"protein_coding","ncbi_id":"23223","summary":null,"start":97356358,"end":97426076,"strand":-1,"description":"ribosomal RNA processing 12 homolog [Source:HGNC Symbol;Acc:HGNC:29100]"}, {"versioned_ensembl_gene_id":"ENSG00000253515.1","gene_symbol":"AC018682.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46499731,"end":46501278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168090.9","gene_symbol":"COPS6","gene_name":"COP9 signalosome subunit 6 [Source:HGNC Symbol;Acc:HGNC:21749]","synonyms":"MOV34-34KD,CSN6","biotype":"protein_coding","ncbi_id":"10980","summary":"The protein encoded by this gene is one of the eight subunits of COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. This protein belongs to translation initiation factor 3 (eIF3) superfamily. It is involved in the regulation of cell cycle and likely to be a cellular cofactor for HIV-1 accessory gene product Vpr. [provided by RefSeq, Jul 2008]","start":100088954,"end":100092200,"strand":1,"description":"COP9 signalosome subunit 6 [Source:HGNC Symbol;Acc:HGNC:21749]"}, {"versioned_ensembl_gene_id":"ENSG00000259194.1","gene_symbol":"AC020891.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51367377,"end":51369110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197254.4","gene_symbol":"AP000445.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58685086,"end":58691861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225705.2","gene_symbol":"AC004899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48846426,"end":48852898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264672.5","gene_symbol":"SEPT4-AS1","gene_name":"SEPT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51345]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927688","summary":null,"start":58519837,"end":58556977,"strand":1,"description":"SEPT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51345]"}, {"versioned_ensembl_gene_id":"ENSG00000250548.6","gene_symbol":"AL355916.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61556313,"end":61570653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177675.8","gene_symbol":"CD163L1","gene_name":"CD163 molecule like 1 [Source:HGNC Symbol;Acc:HGNC:30375]","synonyms":"WC1,SCARI2,M160,CD163B","biotype":"protein_coding","ncbi_id":"283316","summary":"This gene encodes a member of the scavenger receptor cysteine-rich (SRCR) superfamily. Members of this family are secreted or membrane-anchored proteins mainly found in cells associated with the immune system. The SRCR family is defined by a 100-110 amino acid SRCR domain, which may mediate protein-protein interaction and ligand binding. The encoded protein contains twelve SRCR domains, a transmembrane region and a cytoplasmic domain. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":7346685,"end":7479897,"strand":-1,"description":"CD163 molecule like 1 [Source:HGNC Symbol;Acc:HGNC:30375]"}, {"versioned_ensembl_gene_id":"ENSG00000281225.1","gene_symbol":"AL139246.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2492300,"end":2493258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269343.6","gene_symbol":"ZNF587B","gene_name":"zinc finger protein 587B [Source:HGNC Symbol;Acc:HGNC:37142]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100293516","summary":null,"start":57819741,"end":57846238,"strand":1,"description":"zinc finger protein 587B [Source:HGNC Symbol;Acc:HGNC:37142]"}, {"versioned_ensembl_gene_id":"ENSG00000276464.4","gene_symbol":"POMZP3","gene_name":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]","synonyms":"POM121,POM-ZP3","biotype":"protein_coding","ncbi_id":"22932","summary":"This gene appears to have resulted from a fusion of DNA sequences derived from 2 distinct loci, specifically through the duplication of two internal exons from the POM121 gene and four 3' exons from the ZP3 gene. The 5' end of this gene is similar to the 5` coding region of the POM121 gene which encodes an integral nuclear pore membrane protein. However, the protein encoded by this gene lacks the nuclear pore localization motif. The 3' end of this gene is similar to the last 4 exons of the zona pellucida glycoprotein 3 (ZP3) gene and the encoded protein retains one zona pellucida domain. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":76597802,"end":76615077,"strand":-1,"description":"POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:HGNC:9203]"}, {"versioned_ensembl_gene_id":"ENSG00000213157.3","gene_symbol":"AC108734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180887677,"end":180888075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271856.1","gene_symbol":"LINC01215","gene_name":"long intergenic non-protein coding RNA 1215 [Source:HGNC Symbol;Acc:HGNC:49651]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929623","summary":null,"start":108125821,"end":108138610,"strand":1,"description":"long intergenic non-protein coding RNA 1215 [Source:HGNC Symbol;Acc:HGNC:49651]"}, {"versioned_ensembl_gene_id":"ENSG00000240729.1","gene_symbol":"AC146507.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177264766,"end":177265241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279440.1","gene_symbol":"AL008638.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27019369,"end":27024550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235972.1","gene_symbol":"AL355497.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150040547,"end":150042033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237169.1","gene_symbol":"RPL12P27","gene_name":"ribosomal protein L12 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644202","summary":null,"start":97309138,"end":97309958,"strand":-1,"description":"ribosomal protein L12 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36916]"}, {"versioned_ensembl_gene_id":"ENSG00000255482.1","gene_symbol":"AP001830.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102467255,"end":102498801,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255274.9","gene_symbol":"TMPRSS4-AS1","gene_name":"TMPRSS4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526771","summary":null,"start":118003634,"end":118088299,"strand":-1,"description":"TMPRSS4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44179]"}, {"versioned_ensembl_gene_id":"ENSG00000234562.1","gene_symbol":"TPMTP2","gene_name":"thiopurine S-methyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44565]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420393","summary":null,"start":42145646,"end":42146371,"strand":-1,"description":"thiopurine S-methyltransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44565]"}, {"versioned_ensembl_gene_id":"ENSG00000231773.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31370510,"end":31370936,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000236851.1","gene_symbol":"DHFRP2","gene_name":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729816","summary":null,"start":31356448,"end":31356994,"strand":-1,"description":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]"}, {"versioned_ensembl_gene_id":"ENSG00000250968.1","gene_symbol":"LINC02382","gene_name":"long intergenic non-protein coding RNA 2382 [Source:HGNC Symbol;Acc:HGNC:53305]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506107","summary":null,"start":170742469,"end":170743718,"strand":-1,"description":"long intergenic non-protein coding RNA 2382 [Source:HGNC Symbol;Acc:HGNC:53305]"}, {"versioned_ensembl_gene_id":"ENSG00000214203.4","gene_symbol":"RPS4XP1","gene_name":"ribosomal protein S4X pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32444]","synonyms":"RPS4P1","biotype":"processed_pseudogene","ncbi_id":"400064","summary":null,"start":100009052,"end":100009838,"strand":-1,"description":"ribosomal protein S4X pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32444]"}, {"versioned_ensembl_gene_id":"ENSG00000217169.2","gene_symbol":"MTHFD2P2","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48860]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480237","summary":null,"start":87000045,"end":87000291,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48860]"}, {"versioned_ensembl_gene_id":"ENSG00000258289.8","gene_symbol":"CHURC1","gene_name":"churchill domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20099]","synonyms":"My015,FLJ33064,C14orf52","biotype":"protein_coding","ncbi_id":"91612","summary":null,"start":64914361,"end":64944591,"strand":1,"description":"churchill domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20099]"}, {"versioned_ensembl_gene_id":"ENSG00000243955.5","gene_symbol":"GSTA1","gene_name":"glutathione S-transferase alpha 1 [Source:HGNC Symbol;Acc:HGNC:4626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2938","summary":"This gene encodes a member of a family of enzymes that function to add glutathione to target electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins, and products of oxidative stress. This action is an important step in detoxification of these compounds. This subfamily of enzymes has a particular role in protecting cells from reactive oxygen species and the products of peroxidation. Polymorphisms in this gene influence the ability of individuals to metabolize different drugs. This gene is located in a cluster of similar genes and pseudogenes on chromosome 6. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":52791664,"end":52803910,"strand":-1,"description":"glutathione S-transferase alpha 1 [Source:HGNC Symbol;Acc:HGNC:4626]"}, {"versioned_ensembl_gene_id":"ENSG00000249898.7","gene_symbol":"MCPH1-AS1","gene_name":"MCPH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51655]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507530","summary":null,"start":6618475,"end":6708209,"strand":-1,"description":"MCPH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51655]"}, {"versioned_ensembl_gene_id":"ENSG00000166105.15","gene_symbol":"GLB1L3","gene_name":"galactosidase beta 1 like 3 [Source:HGNC Symbol;Acc:HGNC:25147]","synonyms":"FLJ90231","biotype":"protein_coding","ncbi_id":"112937","summary":null,"start":134274245,"end":134319564,"strand":1,"description":"galactosidase beta 1 like 3 [Source:HGNC Symbol;Acc:HGNC:25147]"}, {"versioned_ensembl_gene_id":"ENSG00000231914.1","gene_symbol":"LINC00387","gene_name":"long intergenic non-protein coding RNA 387 [Source:HGNC Symbol;Acc:HGNC:42715]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874152","summary":null,"start":18672827,"end":18676163,"strand":1,"description":"long intergenic non-protein coding RNA 387 [Source:HGNC Symbol;Acc:HGNC:42715]"}, {"versioned_ensembl_gene_id":"ENSG00000271245.1","gene_symbol":"AL136139.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11154929,"end":11155150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251628.1","gene_symbol":"AC106789.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114056006,"end":114057174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169849.8","gene_symbol":"TSPY14P","gene_name":"testis specific protein, Y-linked 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23906]","synonyms":"TSPYP4","biotype":"unprocessed_pseudogene","ncbi_id":"378013","summary":null,"start":21468158,"end":21470683,"strand":1,"description":"testis specific protein, Y-linked 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:23906]"}, {"versioned_ensembl_gene_id":"ENSG00000172296.12","gene_symbol":"SPTLC3","gene_name":"serine palmitoyltransferase long chain base subunit 3 [Source:HGNC Symbol;Acc:HGNC:16253]","synonyms":"SPTLC2L,LCB2B,hLCB2b,FLJ11112,C20orf38","biotype":"protein_coding","ncbi_id":"55304","summary":"This gene encodes a subunit of the serine palmitoyltransferase complex which catalyzes the rate-limiting step in sphingolipid biosynthesis. This subunit metabolizes lauroyl- and myristoyl-CoA and generates C14 and C16-sphingoid bases. [provided by RefSeq, Mar 2017]","start":13008979,"end":13169103,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 3 [Source:HGNC Symbol;Acc:HGNC:16253]"}, {"versioned_ensembl_gene_id":"ENSG00000204113.6","gene_symbol":"BMP2KL","gene_name":"BMP2 inducible kinase-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:17080]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347359","summary":null,"start":74185929,"end":74187153,"strand":1,"description":"BMP2 inducible kinase-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:17080]"}, {"versioned_ensembl_gene_id":"ENSG00000071677.1","gene_symbol":"PRLH","gene_name":"prolactin releasing hormone [Source:HGNC Symbol;Acc:HGNC:17945]","synonyms":"PRH","biotype":"protein_coding","ncbi_id":"51052","summary":null,"start":237566574,"end":237567175,"strand":1,"description":"prolactin releasing hormone [Source:HGNC Symbol;Acc:HGNC:17945]"}, {"versioned_ensembl_gene_id":"ENSG00000126878.12","gene_symbol":"AIF1L","gene_name":"allograft inflammatory factor 1 like [Source:HGNC Symbol;Acc:HGNC:28904]","synonyms":"IBA2,FLJ12783,C9orf58","biotype":"protein_coding","ncbi_id":"83543","summary":null,"start":131096476,"end":131123152,"strand":1,"description":"allograft inflammatory factor 1 like [Source:HGNC Symbol;Acc:HGNC:28904]"}, {"versioned_ensembl_gene_id":"ENSG00000240489.1","gene_symbol":"SETP14","gene_name":"SET pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389168","summary":null,"start":155987304,"end":155988176,"strand":1,"description":"SET pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42933]"}, {"versioned_ensembl_gene_id":"ENSG00000166532.15","gene_symbol":"RIMKLB","gene_name":"ribosomal modification protein rimK like family member B [Source:HGNC Symbol;Acc:HGNC:29228]","synonyms":"NAAGS-I,NAAGS,KIAA1238,FAM80B","biotype":"protein_coding","ncbi_id":"57494","summary":null,"start":8681600,"end":8783095,"strand":1,"description":"ribosomal modification protein rimK like family member B [Source:HGNC Symbol;Acc:HGNC:29228]"}, {"versioned_ensembl_gene_id":"ENSG00000228634.1","gene_symbol":"AL136115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31933020,"end":31933975,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275812.1","gene_symbol":"AL121829.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63543411,"end":63543738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125508.3","gene_symbol":"SRMS","gene_name":"src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites [Source:HGNC Symbol;Acc:HGNC:11298]","synonyms":"SRM,PTK70,dJ697K14.1,C20orf148","biotype":"protein_coding","ncbi_id":"6725","summary":null,"start":63540810,"end":63547504,"strand":-1,"description":"src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites [Source:HGNC Symbol;Acc:HGNC:11298]"}, {"versioned_ensembl_gene_id":"ENSG00000248422.1","gene_symbol":"AC233724.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17598432,"end":17598559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274987.1","gene_symbol":"AC092794.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25210652,"end":25211233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251442.5","gene_symbol":"LINC01094","gene_name":"long intergenic non-protein coding RNA 1094 [Source:HGNC Symbol;Acc:HGNC:49219]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505702","summary":null,"start":78645903,"end":78682699,"strand":1,"description":"long intergenic non-protein coding RNA 1094 [Source:HGNC Symbol;Acc:HGNC:49219]"}, {"versioned_ensembl_gene_id":"ENSG00000251019.1","gene_symbol":"HIGD1AP13","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:43008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874454","summary":null,"start":78648954,"end":78649242,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:43008]"}, {"versioned_ensembl_gene_id":"ENSG00000183242.11","gene_symbol":"WT1-AS","gene_name":"WT1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:18135]","synonyms":"WIT-1,WT1AS,WT1-AS1,WIT1","biotype":"antisense_RNA","ncbi_id":"51352","summary":"This gene is located upstream of the Wilms tumor 1 (WT1) gene; these two genes are bi-directionally transcribed from the same promoter region. This gene is imprinted in kidney, with preferential expression from the paternal allele. Imprinting defects at chromosome 11p13 may contribute to tumorigenesis. [provided by RefSeq, May 2014]","start":32435518,"end":32458769,"strand":1,"description":"WT1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:18135]"}, {"versioned_ensembl_gene_id":"ENSG00000236657.1","gene_symbol":"BX908719.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":33124094,"end":33124608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138587.5","gene_symbol":"MNS1","gene_name":"meiosis specific nuclear structural 1 [Source:HGNC Symbol;Acc:HGNC:29636]","synonyms":"SPATA40,FLJ11222","biotype":"protein_coding","ncbi_id":"55329","summary":"This gene encodes a protein highly similar to the mouse meiosis-specific nuclear structural 1 protein. The mouse protein was shown to be expressed at the pachytene stage during spermatogenesis and may function as a nuclear skeletal protein to regulate nuclear morphology during meiosis. [provided by RefSeq, Oct 2008]","start":56421544,"end":56465137,"strand":-1,"description":"meiosis specific nuclear structural 1 [Source:HGNC Symbol;Acc:HGNC:29636]"}, {"versioned_ensembl_gene_id":"ENSG00000261174.2","gene_symbol":"HMGB1P33","gene_name":"high mobility group box 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39124]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873905","summary":null,"start":56323193,"end":56323719,"strand":1,"description":"high mobility group box 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:39124]"}, {"versioned_ensembl_gene_id":"ENSG00000003056.7","gene_symbol":"M6PR","gene_name":"mannose-6-phosphate receptor, cation dependent [Source:HGNC Symbol;Acc:HGNC:6752]","synonyms":"CD-MPR,CD-M6PR","biotype":"protein_coding","ncbi_id":"4074","summary":"This gene encodes a member of the P-type lectin family. P-type lectins play a critical role in lysosome function through the specific transport of mannose-6-phosphate-containing acid hydrolases from the Golgi complex to lysosomes. The encoded protein functions as a homodimer and requires divalent cations for ligand binding. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, May 2011]","start":8940363,"end":8949955,"strand":-1,"description":"mannose-6-phosphate receptor, cation dependent [Source:HGNC Symbol;Acc:HGNC:6752]"}, {"versioned_ensembl_gene_id":"ENSG00000217776.1","gene_symbol":"AL138827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87070156,"end":87070461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236337.1","gene_symbol":"FMR1-IT1","gene_name":"FMR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41333]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478973","summary":null,"start":147946941,"end":147947583,"strand":1,"description":"FMR1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41333]"}, {"versioned_ensembl_gene_id":"ENSG00000144134.18","gene_symbol":"RABL2A","gene_name":"RAB, member of RAS oncogene family like 2A [Source:HGNC Symbol;Acc:HGNC:9799]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11159","summary":"This gene is a member of the RAB gene family which belongs to the RAS GTPase superfamily. The proteins in the family of RAS-related signaling molecules are small GTP-binding proteins that play important roles in the regulation of exocytotic and endocytotic pathways. This gene maps to the site of an ancestral telomere fusion event and may be a subtelomeric gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":113627229,"end":113643396,"strand":1,"description":"RAB, member of RAS oncogene family like 2A [Source:HGNC Symbol;Acc:HGNC:9799]"}, {"versioned_ensembl_gene_id":"ENSG00000226372.3","gene_symbol":"DCAF8L1","gene_name":"DDB1 and CUL4 associated factor 8 like 1 [Source:HGNC Symbol;Acc:HGNC:31810]","synonyms":"WDR42B","biotype":"protein_coding","ncbi_id":"139425","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate the formation of heterotrimeric or multi-protein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 1. However, the CDS of this intronless gene remains intact, it is conserved in other primate species, it is known to be transcribed, and it is therefore thought to encode a functional protein. [provided by RefSeq, May 2010]","start":27977993,"end":27981449,"strand":-1,"description":"DDB1 and CUL4 associated factor 8 like 1 [Source:HGNC Symbol;Acc:HGNC:31810]"}, {"versioned_ensembl_gene_id":"ENSG00000172348.14","gene_symbol":"RCAN2","gene_name":"regulator of calcineurin 2 [Source:HGNC Symbol;Acc:HGNC:3041]","synonyms":"DSCR1L1,ZAKI-4","biotype":"protein_coding","ncbi_id":"10231","summary":"This gene encodes a member of the regulator of calcineurin (RCAN) protein family. These proteins play a role in many physiological processes by binding to the catalytic domain of calcineurin A, inhibiting calcineurin-mediated nuclear translocation of the transcription factor NFATC1. Expression of this gene in skin fibroblasts is upregulated by thyroid hormone, and the encoded protein may also play a role in endothelial cell function and angiogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":46220736,"end":46491972,"strand":-1,"description":"regulator of calcineurin 2 [Source:HGNC Symbol;Acc:HGNC:3041]"}, {"versioned_ensembl_gene_id":"ENSG00000224589.1","gene_symbol":"AC112492.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27893348,"end":27894059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170442.11","gene_symbol":"KRT86","gene_name":"keratin 86 [Source:HGNC Symbol;Acc:HGNC:6463]","synonyms":"MNX,KRTHB6,Hb6","biotype":"protein_coding","ncbi_id":"3892","summary":"This gene encodes a type II keratin protein, which heterodimerizes with type I keratins to form hair and nails. This gene is present in a cluster of related genes and pseudogenes on chromosome 12. Mutations in this gene have been observed in patients with the hair disease monilethrix. [provided by RefSeq, Feb 2016]","start":52249300,"end":52309163,"strand":1,"description":"keratin 86 [Source:HGNC Symbol;Acc:HGNC:6463]"}, {"versioned_ensembl_gene_id":"ENSG00000108823.15","gene_symbol":"SGCA","gene_name":"sarcoglycan alpha [Source:HGNC Symbol;Acc:HGNC:10805]","synonyms":"ADL,adhalin,A2,SCARMD1,LGMD2D,DMDA2","biotype":"protein_coding","ncbi_id":"6442","summary":"This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":50164214,"end":50175931,"strand":1,"description":"sarcoglycan alpha [Source:HGNC Symbol;Acc:HGNC:10805]"}, {"versioned_ensembl_gene_id":"ENSG00000253262.1","gene_symbol":"AC019176.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5072645,"end":5072869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148484.17","gene_symbol":"RSU1","gene_name":"Ras suppressor protein 1 [Source:HGNC Symbol;Acc:HGNC:10464]","synonyms":"RSP-1,FLJ31034","biotype":"protein_coding","ncbi_id":"6251","summary":"This gene encodes a protein that is involved in the Ras signal transduction pathway, growth inhibition, and nerve-growth factor induced differentiation processes, as determined in mouse and human cell line studies. In mouse, the encoded protein was initially isolated based on its ability to inhibit v-Ras transformation. Multiple alternatively spliced transcript variants for this gene have been reported; one of these variants was found only in glioma tumors. [provided by RefSeq, Jul 2008]","start":16590611,"end":16817528,"strand":-1,"description":"Ras suppressor protein 1 [Source:HGNC Symbol;Acc:HGNC:10464]"}, {"versioned_ensembl_gene_id":"ENSG00000233372.1","gene_symbol":"AL137076.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30140263,"end":30141607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164066.12","gene_symbol":"INTU","gene_name":"inturned planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:29239]","synonyms":"PDZK6,PDZD6,KIAA1284","biotype":"protein_coding","ncbi_id":"27152","summary":null,"start":127623271,"end":127726737,"strand":1,"description":"inturned planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:29239]"}, {"versioned_ensembl_gene_id":"ENSG00000225992.1","gene_symbol":"TRGVA","gene_name":"T-cell receptor gamma variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12296]","synonyms":"V5P,TCRGVA","biotype":"TR_V_pseudogene","ncbi_id":"6986","summary":null,"start":38322446,"end":38322730,"strand":-1,"description":"T-cell receptor gamma variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12296]"}, {"versioned_ensembl_gene_id":"ENSG00000211688.1","gene_symbol":"TRGJP2","gene_name":"T-cell receptor gamma joining P2 [Source:HGNC Symbol;Acc:HGNC:12281]","synonyms":"TCRGJP2,JP2","biotype":"TR_J_gene","ncbi_id":"6972","summary":null,"start":38256337,"end":38256396,"strand":-1,"description":"T-cell receptor gamma joining P2 [Source:HGNC Symbol;Acc:HGNC:12281]"}, {"versioned_ensembl_gene_id":"ENSG00000254853.1","gene_symbol":"AP004247.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58072378,"end":58075438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255565.1","gene_symbol":"AC073651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15780068,"end":15782120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256953.1","gene_symbol":"AC073651.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15813493,"end":15828274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256627.1","gene_symbol":"AC073651.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15803164,"end":15804158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236870.2","gene_symbol":"AL121882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83559896,"end":83560312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233312.8","gene_symbol":"C4B_2","gene_name":"complement component 4B (Chido blood group), copy 2 [Source:HGNC Symbol;Acc:HGNC:42398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100293534","summary":"This gene encodes the basic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. This GeneID and its associated RefSeq record represent a second copy of C4B found on ALT_REF_LOCI_7. [provided by RefSeq, Jul 2011]","start":31974678,"end":31995335,"strand":1,"description":"complement component 4B (Chido blood group), copy 2 [Source:HGNC Symbol;Acc:HGNC:42398]"}, {"versioned_ensembl_gene_id":"ENSG00000119915.4","gene_symbol":"ELOVL3","gene_name":"ELOVL fatty acid elongase 3 [Source:HGNC Symbol;Acc:HGNC:18047]","synonyms":"CIG-30","biotype":"protein_coding","ncbi_id":"83401","summary":"This gene encodes a protein that belongs to the GNS1/SUR4 family. Members of this family play a role in elongation of long chain fatty acids to provide precursors for synthesis of sphingolipids and ceramides. [provided by RefSeq, Jul 2013]","start":102226328,"end":102229589,"strand":1,"description":"ELOVL fatty acid elongase 3 [Source:HGNC Symbol;Acc:HGNC:18047]"}, {"versioned_ensembl_gene_id":"ENSG00000282033.1","gene_symbol":"AC074387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109758799,"end":109760364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279754.1","gene_symbol":"AL162376.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73399031,"end":73399205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255872.3","gene_symbol":"AL138752.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37588413,"end":38068687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204228.3","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"FABGL,SDR30C1,HKE6,D6S2245E,RING2,H2-KE6,KE6","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33204642,"end":33206831,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000196767.6","gene_symbol":"POU3F4","gene_name":"POU class 3 homeobox 4 [Source:HGNC Symbol;Acc:HGNC:9217]","synonyms":"BRN4,OTF9,DFNX2,DFN3","biotype":"protein_coding","ncbi_id":"5456","summary":"This gene encodes a member of the POU-III class of neural transcription factors. This family member plays a role in inner ear development. The protein is thought to be involved in the mediation of epigenetic signals which induce striatal neuron-precursor differentiation. Mutations in this gene are associated with X chromosome-linked nonsyndromic mixed deafness. [provided by RefSeq, Dec 2012]","start":83508250,"end":83512127,"strand":1,"description":"POU class 3 homeobox 4 [Source:HGNC Symbol;Acc:HGNC:9217]"}, {"versioned_ensembl_gene_id":"ENSG00000162747.9","gene_symbol":"FCGR3B","gene_name":"Fc fragment of IgG receptor IIIb [Source:HGNC Symbol;Acc:HGNC:3620]","synonyms":"FCGR3,FCG3,CD16b,CD16","biotype":"protein_coding","ncbi_id":"2215","summary":"The protein encoded by this gene is a low affinity receptor for the Fc region of gamma immunoglobulins (IgG). The encoded protein acts as a monomer and can bind either monomeric or aggregated IgG. This gene may function to capture immune complexes in the peripheral circulation. Several transcript variants encoding different isoforms have been found for this gene. A highly-similar gene encoding a related protein is also found on chromosome 1. [provided by RefSeq, Aug 2012]","start":161623196,"end":161631963,"strand":-1,"description":"Fc fragment of IgG receptor IIIb [Source:HGNC Symbol;Acc:HGNC:3620]"}, {"versioned_ensembl_gene_id":"ENSG00000119397.16","gene_symbol":"CNTRL","gene_name":"centriolin [Source:HGNC Symbol;Acc:HGNC:1858]","synonyms":"CEP110,CEP1","biotype":"protein_coding","ncbi_id":"11064","summary":"This gene encodes a centrosomal protein required for the centrosome to function as a microtubule organizing center. The gene product is also associated with centrosome maturation. One version of stem cell myeloproliferative disorder is the result of a reciprocal translocation between chromosomes 8 and 9, with the breakpoint associated with fibroblast growth factor receptor 1 and centrosomal protein 1. [provided by RefSeq, Jul 2008]","start":121074863,"end":121177610,"strand":1,"description":"centriolin [Source:HGNC Symbol;Acc:HGNC:1858]"}, {"versioned_ensembl_gene_id":"ENSG00000259198.1","gene_symbol":"AC020658.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40312615,"end":40316634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259848.8","gene_symbol":"AC097374.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94867486,"end":94947341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146373.16","gene_symbol":"RNF217","gene_name":"ring finger protein 217 [Source:HGNC Symbol;Acc:HGNC:21487]","synonyms":"MGC26996,IBRDC1,dJ84N20.1,C6orf172","biotype":"protein_coding","ncbi_id":"154214","summary":"This protein encoded by this gene is a member of the RING1-IBR-RING24 (RBR) ubiquitin protein ligase family, and it belongs to a subfamily of these proteins that contain a transmembrane domain. This protein can interact with the HAX1 anti-apoptotic protein via its C-terminal RING finger motif, which suggests a role in apoptosis signaling. It is thought that deregulation of this gene can be a mechanism in leukemogenesis. Mutations in the region encoding the protein GXXXG motif, which appears to be necessary for protein self-association, have been found in human cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":124962545,"end":125092633,"strand":1,"description":"ring finger protein 217 [Source:HGNC Symbol;Acc:HGNC:21487]"}, {"versioned_ensembl_gene_id":"ENSG00000178015.4","gene_symbol":"GPR150","gene_name":"G protein-coupled receptor 150 [Source:HGNC Symbol;Acc:HGNC:23628]","synonyms":"PGR11","biotype":"protein_coding","ncbi_id":"285601","summary":"This gene encodes an orphan member of the class A rhodopsin-like family of G-protein-coupled receptors (GPCRs). Within the rhodopsin-like family, this gene is a member of the vasopressin-like subfamily that also includes vasopressin and oxytocin receptors. The silencing of this gene, due to promoter methylation, is associated with ovarian cancer progression. All GPCRs have a transmembrane domain that includes seven transmembrane alpha-helices. A general feature of GPCR signaling is the agonist-induced conformational change in the receptor, leading to activation of the heterotrimeric G protein. The activated G protein then binds to and activates numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017]","start":95620078,"end":95622142,"strand":1,"description":"G protein-coupled receptor 150 [Source:HGNC Symbol;Acc:HGNC:23628]"}, {"versioned_ensembl_gene_id":"ENSG00000236548.1","gene_symbol":"RNF217-AS1","gene_name":"RNF217 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50866]","synonyms":"STL","biotype":"antisense_RNA","ncbi_id":"7955","summary":null,"start":124909093,"end":124963039,"strand":-1,"description":"RNF217 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50866]"}, {"versioned_ensembl_gene_id":"ENSG00000280233.1","gene_symbol":"AC015813.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57988180,"end":57988760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231791.1","gene_symbol":"AL445228.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184329071,"end":184332826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282235.1","gene_symbol":"AC240565.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64099,"end":76866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267557.1","gene_symbol":"AC008474.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32666298,"end":32673210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101680.14","gene_symbol":"LAMA1","gene_name":"laminin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6481]","synonyms":"LAMA","biotype":"protein_coding","ncbi_id":"284217","summary":"This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome. [provided by RefSeq, Sep 2014]","start":6941744,"end":7117814,"strand":-1,"description":"laminin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6481]"}, {"versioned_ensembl_gene_id":"ENSG00000131015.4","gene_symbol":"ULBP2","gene_name":"UL16 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14894]","synonyms":"RAET1H","biotype":"protein_coding","ncbi_id":"80328","summary":"This gene encodes a major histocompatibility complex (MHC) class I-related molecule that binds to the NKG2D receptor on natural killer (NK) cells to trigger release of multiple cytokines and chemokines that in turn contribute to the recruitment and activation of NK cells. The encoded protein undergoes further processing to generate the mature protein that is either anchored to membrane via a glycosylphosphatidylinositol moiety, or secreted. Many malignant cells secrete the encoded protein to evade immunosurveillance by NK cells. This gene is located in a cluster of multiple MHC class I-related genes on chromosome 6. [provided by RefSeq, Jul 2015]","start":149942000,"end":149949235,"strand":1,"description":"UL16 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:14894]"}, {"versioned_ensembl_gene_id":"ENSG00000241404.6","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"C6orf8,NG3","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32164583,"end":32168281,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000179935.9","gene_symbol":"LINC00652","gene_name":"long intergenic non-protein coding RNA 652 [Source:HGNC Symbol;Acc:HGNC:25003]","synonyms":"HSPC072","biotype":"lincRNA","ncbi_id":"29075","summary":null,"start":18786065,"end":18794335,"strand":-1,"description":"long intergenic non-protein coding RNA 652 [Source:HGNC Symbol;Acc:HGNC:25003]"}, {"versioned_ensembl_gene_id":"ENSG00000233111.1","gene_symbol":"RAB1C","gene_name":"RAB1C, member RAS oncogene family pseudogene [Source:HGNC Symbol;Acc:HGNC:23683]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441400","summary":null,"start":37636688,"end":37637293,"strand":-1,"description":"RAB1C, member RAS oncogene family pseudogene [Source:HGNC Symbol;Acc:HGNC:23683]"}, {"versioned_ensembl_gene_id":"ENSG00000079785.14","gene_symbol":"DDX1","gene_name":"DEAD-box helicase 1 [Source:HGNC Symbol;Acc:HGNC:2734]","synonyms":"DBP-RB","biotype":"protein_coding","ncbi_id":"1653","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein of unknown function. It shows high transcription levels in 2 retinoblastoma cell lines and in tissues of neuroectodermal origin. [provided by RefSeq, Jul 2008]","start":15591178,"end":15631111,"strand":1,"description":"DEAD-box helicase 1 [Source:HGNC Symbol;Acc:HGNC:2734]"}, {"versioned_ensembl_gene_id":"ENSG00000216621.8","gene_symbol":"AL583835.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":149934527,"end":149936782,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216713.1","gene_symbol":"MTND4P13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42222]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862853","summary":null,"start":153668879,"end":153669901,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42222]"}, {"versioned_ensembl_gene_id":"ENSG00000258741.3","gene_symbol":"AC091544.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":92715710,"end":92734195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240922.1","gene_symbol":"LSAMP-AS1","gene_name":"LSAMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40350]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926903","summary":null,"start":116360024,"end":116370090,"strand":1,"description":"LSAMP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40350]"}, {"versioned_ensembl_gene_id":"ENSG00000278860.1","gene_symbol":"AC005691.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34614409,"end":34614809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168878.16","gene_symbol":"SFTPB","gene_name":"surfactant protein B [Source:HGNC Symbol;Acc:HGNC:10801]","synonyms":"SP-B,SFTP3","biotype":"protein_coding","ncbi_id":"6439","summary":"This gene encodes the pulmonary-associated surfactant protein B (SPB), an amphipathic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. The SPB enhances the rate of spreading and increases the stability of surfactant monolayers in vitro. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 1, also called pulmonary alveolar proteinosis due to surfactant protein B deficiency, and are associated with fatal respiratory distress in the neonatal period. Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq, Feb 2010]","start":85657314,"end":85668741,"strand":-1,"description":"surfactant protein B [Source:HGNC Symbol;Acc:HGNC:10801]"}, {"versioned_ensembl_gene_id":"ENSG00000282237.1","gene_symbol":"AC015938.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36723427,"end":36727184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214313.8","gene_symbol":"AZGP1P1","gene_name":"alpha-2-glycoprotein 1, zinc-binding pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:911]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646282","summary":null,"start":99980762,"end":99987535,"strand":1,"description":"alpha-2-glycoprotein 1, zinc-binding pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:911]"}, {"versioned_ensembl_gene_id":"ENSG00000235621.8","gene_symbol":"LINC00494","gene_name":"long intergenic non-protein coding RNA 494 [Source:HGNC Symbol;Acc:HGNC:27657]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284749","summary":null,"start":48359950,"end":48370629,"strand":1,"description":"long intergenic non-protein coding RNA 494 [Source:HGNC Symbol;Acc:HGNC:27657]"}, {"versioned_ensembl_gene_id":"ENSG00000143252.14","gene_symbol":"SDHC","gene_name":"succinate dehydrogenase complex subunit C [Source:HGNC Symbol;Acc:HGNC:10682]","synonyms":"PGL3,cybL,CYB560","biotype":"protein_coding","ncbi_id":"6391","summary":"This gene encodes one of four nuclear-encoded subunits that comprise succinate dehydrogenase, also known as mitochondrial complex II, a key enzyme complex of the tricarboxylic acid cycle and aerobic respiratory chains of mitochondria. The encoded protein is one of two integral membrane proteins that anchor other subunits of the complex, which form the catalytic core, to the inner mitochondrial membrane. There are several related pseudogenes for this gene on different chromosomes. Mutations in this gene have been associated with paragangliomas. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2013]","start":161314257,"end":161375340,"strand":1,"description":"succinate dehydrogenase complex subunit C [Source:HGNC Symbol;Acc:HGNC:10682]"}, {"versioned_ensembl_gene_id":"ENSG00000254545.1","gene_symbol":"AL354919.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31789130,"end":31791322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161634.11","gene_symbol":"DCD","gene_name":"dermcidin [Source:HGNC Symbol;Acc:HGNC:14669]","synonyms":"PIF,HCAP,DSEP,DCD-1,AIDD","biotype":"protein_coding","ncbi_id":"117159","summary":"This antimicrobial gene encodes a secreted protein that is subsequently processed into mature peptides of distinct biological activities. The C-terminal peptide is constitutively expressed in sweat and has antibacterial and antifungal activities. The N-terminal peptide, also known as diffusible survival evasion peptide, promotes neural cell survival under conditions of severe oxidative stress. A glycosylated form of the N-terminal peptide may be associated with cachexia (muscle wasting) in cancer patients. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":54644591,"end":54648493,"strand":-1,"description":"dermcidin [Source:HGNC Symbol;Acc:HGNC:14669]"}, {"versioned_ensembl_gene_id":"ENSG00000118507.15","gene_symbol":"AKAP7","gene_name":"A-kinase anchoring protein 7 [Source:HGNC Symbol;Acc:HGNC:377]","synonyms":"AKAP18,AKAP15","biotype":"protein_coding","ncbi_id":"9465","summary":"This gene encodes a member of the A-kinase anchoring protein (AKAP) family, a group of functionally related proteins that bind to a regulatory subunit (RII) of cAMP-dependent protein kinase A (PKA) and target the enzyme to specific subcellular compartments. AKAPs have a common RII-binding domain, but contain different targeting motifs responsible for directing PKA to distinct intracellular locations. Three alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Apr 2011]","start":131135666,"end":131283535,"strand":1,"description":"A-kinase anchoring protein 7 [Source:HGNC Symbol;Acc:HGNC:377]"}, {"versioned_ensembl_gene_id":"ENSG00000276923.1","gene_symbol":"AL139351.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48073869,"end":48074188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126814.6","gene_symbol":"TRMT5","gene_name":"tRNA methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:23141]","synonyms":"TRM5,KIAA1393","biotype":"protein_coding","ncbi_id":"57570","summary":"tRNAs contain as many as 13 or 14 nucleotides that are modified posttranscriptionally by enzymes that are highly specific for particular nucleotides in the tRNA structure. TRMT5 methylates the N1 position of guanosine-37 (G37) in selected tRNAs using S-adenosyl methionine (Brule et al., 2004 [PubMed 15248782]).[supplied by OMIM, Mar 2008]","start":60971451,"end":60981358,"strand":-1,"description":"tRNA methyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:23141]"}, {"versioned_ensembl_gene_id":"ENSG00000135346.8","gene_symbol":"CGA","gene_name":"glycoprotein hormones, alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:1885]","synonyms":"TSHA,LHA,HCG,GPHA1,GPHa,FSHA","biotype":"protein_coding","ncbi_id":"1081","summary":"The four human glycoprotein hormones chorionic gonadotropin (CG), luteinizing hormone (LH), follicle stimulating hormone (FSH), and thyroid stimulating hormone (TSH) are dimers consisting of alpha and beta subunits that are associated noncovalently. The alpha subunits of these hormones are identical, however, their beta chains are unique and confer biological specificity. The protein encoded by this gene is the alpha subunit and belongs to the glycoprotein hormones alpha chain family. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":87085498,"end":87095406,"strand":-1,"description":"glycoprotein hormones, alpha polypeptide [Source:HGNC Symbol;Acc:HGNC:1885]"}, {"versioned_ensembl_gene_id":"ENSG00000257403.2","gene_symbol":"AC008740.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21347139,"end":21352138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145414.8","gene_symbol":"NAF1","gene_name":"nuclear assembly factor 1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:25126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92345","summary":null,"start":163110073,"end":163166921,"strand":-1,"description":"nuclear assembly factor 1 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:25126]"}, {"versioned_ensembl_gene_id":"ENSG00000167210.16","gene_symbol":"LOXHD1","gene_name":"lipoxygenase homology domains 1 [Source:HGNC Symbol;Acc:HGNC:26521]","synonyms":"LH2D1,FLJ32670,DFNB77","biotype":"protein_coding","ncbi_id":"125336","summary":"This gene encodes a highly conserved protein consisting entirely of PLAT (polycystin/lipoxygenase/alpha-toxin) domains, thought to be involved in targeting proteins to the plasma membrane. Studies in mice show that this gene is expressed in the mechanosensory hair cells in the inner ear, and mutations in this gene lead to auditory defects, indicating that this gene is essential for normal hair cell function. Screening of human families segregating deafness identified a mutation in this gene which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL). Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010]","start":46476972,"end":46657033,"strand":-1,"description":"lipoxygenase homology domains 1 [Source:HGNC Symbol;Acc:HGNC:26521]"}, {"versioned_ensembl_gene_id":"ENSG00000235447.2","gene_symbol":"TRAPPC13P1","gene_name":"trafficking protein particle complex 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50347]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646193","summary":null,"start":76655498,"end":76656559,"strand":-1,"description":"trafficking protein particle complex 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50347]"}, {"versioned_ensembl_gene_id":"ENSG00000273110.1","gene_symbol":"AL162591.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154480012,"end":154481501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274844.1","gene_symbol":"AL512427.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60826185,"end":60826533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236887.1","gene_symbol":"AL357055.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113198825,"end":113199258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102390.10","gene_symbol":"PBDC1","gene_name":"polysaccharide biosynthesis domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28790]","synonyms":"MGC874,CXorf26","biotype":"protein_coding","ncbi_id":"51260","summary":null,"start":76172936,"end":76178204,"strand":1,"description":"polysaccharide biosynthesis domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28790]"}, {"versioned_ensembl_gene_id":"ENSG00000233839.1","gene_symbol":"AL357055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113168994,"end":113169403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281548.1","gene_symbol":"LINC00895","gene_name":"long intergenic non-protein coding RNA 895 [Source:HGNC Symbol;Acc:HGNC:48580]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150185","summary":null,"start":19565203,"end":19566839,"strand":-1,"description":"long intergenic non-protein coding RNA 895 [Source:HGNC Symbol;Acc:HGNC:48580]"}, {"versioned_ensembl_gene_id":"ENSG00000095539.15","gene_symbol":"SEMA4G","gene_name":"semaphorin 4G [Source:HGNC Symbol;Acc:HGNC:10735]","synonyms":"KIAA1619,FLJ20590","biotype":"protein_coding","ncbi_id":"57715","summary":"Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":100969518,"end":100985871,"strand":1,"description":"semaphorin 4G [Source:HGNC Symbol;Acc:HGNC:10735]"}, {"versioned_ensembl_gene_id":"ENSG00000277494.1","gene_symbol":"GPIHBP1","gene_name":"glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24945]","synonyms":"LOC338328,GPI-HBP1","biotype":"protein_coding","ncbi_id":"338328","summary":"This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) family. This protein plays a major role in transporting lipoprotein lipase (LPL) from the subendothelial spaces to the capillary lumen. Mutations in this gene are the cause of hyperlipoproteinemia, type 1D. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":143213193,"end":143217170,"strand":1,"description":"glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24945]"}, {"versioned_ensembl_gene_id":"ENSG00000235439.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"BAT1,UAP56,D6S81E","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31520968,"end":31533197,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000270449.1","gene_symbol":"AP001485.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104682383,"end":104682581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166348.18","gene_symbol":"USP54","gene_name":"ubiquitin specific peptidase 54 [Source:HGNC Symbol;Acc:HGNC:23513]","synonyms":"FLJ37318,C10orf29,bA137L10.4,bA137L10.3","biotype":"protein_coding","ncbi_id":"159195","summary":null,"start":73497538,"end":73625953,"strand":-1,"description":"ubiquitin specific peptidase 54 [Source:HGNC Symbol;Acc:HGNC:23513]"}, {"versioned_ensembl_gene_id":"ENSG00000073861.2","gene_symbol":"TBX21","gene_name":"T-box 21 [Source:HGNC Symbol;Acc:HGNC:11599]","synonyms":"TBLYM,T-bet","biotype":"protein_coding","ncbi_id":"30009","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is the human ortholog of mouse Tbx21/Tbet gene. Studies in mouse show that Tbx21 protein is a Th1 cell-specific transcription factor that controls the expression of the hallmark Th1 cytokine, interferon-gamma (IFNG). Expression of the human ortholog also correlates with IFNG expression in Th1 and natural killer cells, suggesting a role for this gene in initiating Th1 lineage development from naive Th precursor cells. [provided by RefSeq, Jul 2008]","start":47733244,"end":47746119,"strand":1,"description":"T-box 21 [Source:HGNC Symbol;Acc:HGNC:11599]"}, {"versioned_ensembl_gene_id":"ENSG00000261587.2","gene_symbol":"TMEM249","gene_name":"transmembrane protein 249 [Source:HGNC Symbol;Acc:HGNC:44155]","synonyms":"C8orfK29","biotype":"protein_coding","ncbi_id":"340393","summary":null,"start":144352219,"end":144354914,"strand":-1,"description":"transmembrane protein 249 [Source:HGNC Symbol;Acc:HGNC:44155]"}, {"versioned_ensembl_gene_id":"ENSG00000129173.12","gene_symbol":"E2F8","gene_name":"E2F transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24727]","synonyms":"FLJ23311","biotype":"protein_coding","ncbi_id":"79733","summary":"This gene encodes a member of a family of transcription factors which regulate the expression of genes required for progression through the cell cycle. The encoded protein regulates progression from G1 to S phase by ensuring the nucleus divides at the proper time. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2012]","start":19224063,"end":19241620,"strand":-1,"description":"E2F transcription factor 8 [Source:HGNC Symbol;Acc:HGNC:24727]"}, {"versioned_ensembl_gene_id":"ENSG00000033178.12","gene_symbol":"UBA6","gene_name":"ubiquitin like modifier activating enzyme 6 [Source:HGNC Symbol;Acc:HGNC:25581]","synonyms":"FLJ10808,UBE1L2","biotype":"protein_coding","ncbi_id":"55236","summary":"Modification of proteins with ubiquitin (UBB; MIM 191339) or ubiquitin-like proteins controls many signaling networks and requires a ubiquitin-activating enzyme (E1), a ubiquitin conjugating enzyme (E2), and a ubiquitin protein ligase (E3). UBE1L2 is an E1 enzyme that initiates the activation and conjugation of ubiquitin-like proteins (Jin et al., 2007 [PubMed 17597759]).[supplied by OMIM, Mar 2008]","start":67612652,"end":67701179,"strand":-1,"description":"ubiquitin like modifier activating enzyme 6 [Source:HGNC Symbol;Acc:HGNC:25581]"}, {"versioned_ensembl_gene_id":"ENSG00000198000.11","gene_symbol":"NOL8","gene_name":"nucleolar protein 8 [Source:HGNC Symbol;Acc:HGNC:23387]","synonyms":"FLJ20736,C9orf34,Nop132","biotype":"protein_coding","ncbi_id":"55035","summary":"NOL8 binds Ras-related GTP-binding proteins (see MIM 608267) and plays a role in cell growth (Sekiguchi et al., 2004 [PubMed 14660641]).[supplied by OMIM, Mar 2008]","start":92297358,"end":92325636,"strand":-1,"description":"nucleolar protein 8 [Source:HGNC Symbol;Acc:HGNC:23387]"}, {"versioned_ensembl_gene_id":"ENSG00000254855.1","gene_symbol":"AP001107.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66264777,"end":66265666,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234398.1","gene_symbol":"AC134915.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130245971,"end":130248770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164919.10","gene_symbol":"COX6C","gene_name":"cytochrome c oxidase subunit 6C [Source:HGNC Symbol;Acc:HGNC:2285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1345","summary":"Cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes subunit VIc, which has 77% amino acid sequence identity with mouse subunit VIc. This gene is up-regulated in prostate cancer cells. A pseudogene has been found on chromosomes 16p12. [provided by RefSeq, Jul 2010]","start":99873200,"end":99894062,"strand":-1,"description":"cytochrome c oxidase subunit 6C [Source:HGNC Symbol;Acc:HGNC:2285]"}, {"versioned_ensembl_gene_id":"ENSG00000269055.1","gene_symbol":"BNIP3P18","gene_name":"BCL2 interacting protein 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49698]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481693","summary":null,"start":20267817,"end":20268391,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49698]"}, {"versioned_ensembl_gene_id":"ENSG00000158122.11","gene_symbol":"AAED1","gene_name":"AhpC/TSA antioxidant enzyme domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16881]","synonyms":"C9orf21","biotype":"protein_coding","ncbi_id":"195827","summary":null,"start":96639577,"end":96655303,"strand":-1,"description":"AhpC/TSA antioxidant enzyme domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16881]"}, {"versioned_ensembl_gene_id":"ENSG00000268620.1","gene_symbol":"AC078899.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20249052,"end":20250295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161010.14","gene_symbol":"MRNIP","gene_name":"MRN complex interacting protein [Source:HGNC Symbol;Acc:HGNC:30817]","synonyms":"MGC78537,MGC65027,LOC51149,DKFZp686L2452,C5orf45","biotype":"protein_coding","ncbi_id":"51149","summary":null,"start":179835133,"end":179862173,"strand":-1,"description":"MRN complex interacting protein [Source:HGNC Symbol;Acc:HGNC:30817]"}, {"versioned_ensembl_gene_id":"ENSG00000227394.1","gene_symbol":"AC007386.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64960053,"end":64960634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254885.1","gene_symbol":"AP001547.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79191558,"end":79193160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060642.10","gene_symbol":"PIGV","gene_name":"phosphatidylinositol glycan anchor biosynthesis class V [Source:HGNC Symbol;Acc:HGNC:26031]","synonyms":"FLJ20477","biotype":"protein_coding","ncbi_id":"55650","summary":"This gene encodes a mannosyltransferase enzyme involved in the biosynthesis of glycosylphosphatidylinositol (GPI). GPI is a complex glycolipid that functions as a membrane anchor for many proteins and plays a role in multiple cellular processes including protein sorting and signal transduction. The encoded protein is localized to the endoplasmic reticulum and transfers the second mannose to the GPI backbone. Mutations in this gene are associated with hyperphosphatasia cognitive disability syndrome. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]","start":26787472,"end":26798398,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class V [Source:HGNC Symbol;Acc:HGNC:26031]"}, {"versioned_ensembl_gene_id":"ENSG00000119509.12","gene_symbol":"INVS","gene_name":"inversin [Source:HGNC Symbol;Acc:HGNC:17870]","synonyms":"NPHP2","biotype":"protein_coding","ncbi_id":"27130","summary":"This gene encodes a protein containing multiple ankyrin domains and two IQ calmodulin-binding domains. The encoded protein may function in renal tubular development and function, and in left-right axis determination. This protein interacts with nephrocystin and infers a connection between primary cilia function and left-right axis determination. A similar protein in mice interacts with calmodulin. Mutations in this gene have been associated with nephronophthisis type 2. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, May 2012]","start":100099256,"end":100301000,"strand":1,"description":"inversin [Source:HGNC Symbol;Acc:HGNC:17870]"}, {"versioned_ensembl_gene_id":"ENSG00000144015.4","gene_symbol":"TRIM43","gene_name":"tripartite motif containing 43 [Source:HGNC Symbol;Acc:HGNC:19015]","synonyms":"TRIM43A","biotype":"protein_coding","ncbi_id":"129868","summary":null,"start":95592018,"end":95599778,"strand":1,"description":"tripartite motif containing 43 [Source:HGNC Symbol;Acc:HGNC:19015]"}, {"versioned_ensembl_gene_id":"ENSG00000253121.1","gene_symbol":"AC120042.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63024372,"end":63025294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227772.8","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31488846,"end":31501875,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000283463.1","gene_symbol":"HSFX4","gene_name":"heat shock transcription factor family, X-linked member 4 [Source:HGNC Symbol;Acc:HGNC:52398]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101927685","summary":null,"start":149929645,"end":149931287,"strand":1,"description":"heat shock transcription factor family, X-linked member 4 [Source:HGNC Symbol;Acc:HGNC:52398]"}, {"versioned_ensembl_gene_id":"ENSG00000166927.12","gene_symbol":"MS4A7","gene_name":"membrane spanning 4-domains A7 [Source:HGNC Symbol;Acc:HGNC:13378]","synonyms":"MS4A8,CFFM4,CD20L4","biotype":"protein_coding","ncbi_id":"58475","summary":"This gene encodes a member of the membrane-spanning 4A gene family, members of which are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns in hematopoietic cells and nonlymphoid tissues. This family member is associated with mature cellular function in the monocytic lineage, and it may be a component of a receptor complex involved in signal transduction. This gene is localized to 11q12, in a cluster of other family members. At least four alternatively spliced transcript variants encoding two distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":60378482,"end":60395951,"strand":1,"description":"membrane spanning 4-domains A7 [Source:HGNC Symbol;Acc:HGNC:13378]"}, {"versioned_ensembl_gene_id":"ENSG00000183206.17","gene_symbol":"POTEC","gene_name":"POTE ankyrin domain family member C [Source:HGNC Symbol;Acc:HGNC:33894]","synonyms":"POTE18,POTE-18,DKFZp686J0529,CT104.6,A26B2","biotype":"protein_coding","ncbi_id":"388468","summary":null,"start":14507339,"end":14543585,"strand":-1,"description":"POTE ankyrin domain family member C [Source:HGNC Symbol;Acc:HGNC:33894]"}, {"versioned_ensembl_gene_id":"ENSG00000235266.1","gene_symbol":"RPL22P17","gene_name":"ribosomal protein L22 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36985]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271289","summary":null,"start":102887874,"end":102888188,"strand":-1,"description":"ribosomal protein L22 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36985]"}, {"versioned_ensembl_gene_id":"ENSG00000258033.1","gene_symbol":"AC063947.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101066734,"end":101069232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225017.1","gene_symbol":"AP004289.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99346052,"end":99348256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180902.17","gene_symbol":"D2HGDH","gene_name":"D-2-hydroxyglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:28358]","synonyms":"D2HGD,MGC25181,FLJ42195","biotype":"protein_coding","ncbi_id":"728294","summary":"This gene encodes D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features. [provided by RefSeq, Jul 2008]","start":241734579,"end":241768816,"strand":1,"description":"D-2-hydroxyglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:28358]"}, {"versioned_ensembl_gene_id":"ENSG00000171631.14","gene_symbol":"P2RY6","gene_name":"pyrimidinergic receptor P2Y6 [Source:HGNC Symbol;Acc:HGNC:8543]","synonyms":"P2Y6","biotype":"protein_coding","ncbi_id":"5031","summary":"The product of this gene belongs to the family of P2 receptors, which is activated by extracellular nucleotides and subdivided into P2X ligand-gated ion channels and P2Y G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor, which is a G-protein coupled receptor, is responsive to UDP, partially responsive to UTP and ADP, and not responsive to ATP. It is proposed that this receptor mediates inflammatory responses. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Mar 2013]","start":73264505,"end":73298617,"strand":1,"description":"pyrimidinergic receptor P2Y6 [Source:HGNC Symbol;Acc:HGNC:8543]"}, {"versioned_ensembl_gene_id":"ENSG00000233355.6","gene_symbol":"CHRM3-AS2","gene_name":"CHRM3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43725]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506915","summary":null,"start":239703381,"end":239730465,"strand":-1,"description":"CHRM3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43725]"}, {"versioned_ensembl_gene_id":"ENSG00000204971.3","gene_symbol":"AP000812.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72163322,"end":72209241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223869.1","gene_symbol":"AC099563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":214943123,"end":214943540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197226.12","gene_symbol":"TBC1D9B","gene_name":"TBC1 domain family member 9B [Source:HGNC Symbol;Acc:HGNC:29097]","synonyms":"KIAA0676,GRAMD9B","biotype":"protein_coding","ncbi_id":"23061","summary":null,"start":179862066,"end":179907859,"strand":-1,"description":"TBC1 domain family member 9B [Source:HGNC Symbol;Acc:HGNC:29097]"}, {"versioned_ensembl_gene_id":"ENSG00000271824.1","gene_symbol":"AC009014.1","gene_name":"Homo sapiens uncharacterized LOC389332 (LOC389332), mRNA. [Source:RefSeq mRNA;Acc:NM_001350994]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136191468,"end":136193134,"strand":-1,"description":"Homo sapiens uncharacterized LOC389332 (LOC389332), mRNA. [Source:RefSeq mRNA;Acc:NM_001350994]"}, {"versioned_ensembl_gene_id":"ENSG00000179774.8","gene_symbol":"ATOH7","gene_name":"atonal bHLH transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:13907]","synonyms":"Math5,bHLHa13","biotype":"protein_coding","ncbi_id":"220202","summary":"This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Studies in mice suggest that this gene plays a central role in retinal ganglion cell and optic nerve formation. Mutations in this gene are associated with nonsyndromic congenital retinal nonattachment. [provided by RefSeq, Dec 2011]","start":68230624,"end":68232103,"strand":-1,"description":"atonal bHLH transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:13907]"}, {"versioned_ensembl_gene_id":"ENSG00000080511.3","gene_symbol":"RDH8","gene_name":"retinol dehydrogenase 8 (all-trans) [Source:HGNC Symbol;Acc:HGNC:14423]","synonyms":"SDR28C2,PRRDH","biotype":"protein_coding","ncbi_id":"50700","summary":"This gene encodes a member of the short-chain dehydrogenase/reductase family. The encoded protein catalyzes the reduction of all-trans-retinal to all-trans-retinol, the first reaction step of the rhodopsin regeneration pathway. This enzymatic reaction is the rate-limiting step in the visual cycle. [provided by RefSeq, Feb 2014]","start":10013249,"end":10022279,"strand":1,"description":"retinol dehydrogenase 8 (all-trans) [Source:HGNC Symbol;Acc:HGNC:14423]"}, {"versioned_ensembl_gene_id":"ENSG00000164270.17","gene_symbol":"HTR4","gene_name":"5-hydroxytryptamine receptor 4 [Source:HGNC Symbol;Acc:HGNC:5299]","synonyms":"5-HT4","biotype":"protein_coding","ncbi_id":"3360","summary":"This gene is a member of the family of serotonin receptors, which are G protein coupled receptors that stimulate cAMP production in response to serotonin (5-hydroxytryptamine). The gene product is a glycosylated transmembrane protein that functions in both the peripheral and central nervous system to modulate the release of various neurotransmitters. Multiple transcript variants encoding proteins with distinct C-terminal sequences have been described. [provided by RefSeq, May 2010]","start":148451032,"end":148677235,"strand":-1,"description":"5-hydroxytryptamine receptor 4 [Source:HGNC Symbol;Acc:HGNC:5299]"}, {"versioned_ensembl_gene_id":"ENSG00000279065.1","gene_symbol":"AL138688.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20194412,"end":20196005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273747.1","gene_symbol":"AC022558.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83020115,"end":83020802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269887.1","gene_symbol":"AL391001.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":164680085,"end":164680799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203485.12","gene_symbol":"INF2","gene_name":"inverted formin, FH2 and WH2 domain containing [Source:HGNC Symbol;Acc:HGNC:23791]","synonyms":"MGC13251,C14orf173,C14orf151","biotype":"protein_coding","ncbi_id":"64423","summary":"This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.[provided by RefSeq, Aug 2010]","start":104689606,"end":104722535,"strand":1,"description":"inverted formin, FH2 and WH2 domain containing [Source:HGNC Symbol;Acc:HGNC:23791]"}, {"versioned_ensembl_gene_id":"ENSG00000271749.1","gene_symbol":"AC005828.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63393355,"end":63393586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279951.1","gene_symbol":"AL138688.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20092632,"end":20094144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235947.1","gene_symbol":"EGOT","gene_name":"eosinophil granule ontogeny transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37129]","synonyms":"NCRNA00190,EGO","biotype":"lincRNA","ncbi_id":"100126791","summary":null,"start":4749192,"end":4751590,"strand":-1,"description":"eosinophil granule ontogeny transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37129]"}, {"versioned_ensembl_gene_id":"ENSG00000224647.2","gene_symbol":"AC026954.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":7330452,"end":7335413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260923.6","gene_symbol":"LINC02193","gene_name":"long intergenic non-protein coding RNA 2193 [Source:HGNC Symbol;Acc:HGNC:53055]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371423","summary":null,"start":90173217,"end":90222678,"strand":1,"description":"long intergenic non-protein coding RNA 2193 [Source:HGNC Symbol;Acc:HGNC:53055]"}, {"versioned_ensembl_gene_id":"ENSG00000134899.18","gene_symbol":"ERCC5","gene_name":"ERCC excision repair 5, endonuclease [Source:HGNC Symbol;Acc:HGNC:3437]","synonyms":"XPGC,ERCM2","biotype":"protein_coding","ncbi_id":"2073","summary":"This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011]","start":102844844,"end":102876001,"strand":1,"description":"ERCC excision repair 5, endonuclease [Source:HGNC Symbol;Acc:HGNC:3437]"}, {"versioned_ensembl_gene_id":"ENSG00000257389.1","gene_symbol":"AC107016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52837403,"end":52837739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223561.6","gene_symbol":"AC005165.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25593351,"end":25750994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148735.14","gene_symbol":"PLEKHS1","gene_name":"pleckstrin homology domain containing S1 [Source:HGNC Symbol;Acc:HGNC:26285]","synonyms":"FLJ23537,C10orf81,bA211N11.2","biotype":"protein_coding","ncbi_id":"79949","summary":null,"start":113751454,"end":113783429,"strand":1,"description":"pleckstrin homology domain containing S1 [Source:HGNC Symbol;Acc:HGNC:26285]"}, {"versioned_ensembl_gene_id":"ENSG00000103160.11","gene_symbol":"HSDL1","gene_name":"hydroxysteroid dehydrogenase like 1 [Source:HGNC Symbol;Acc:HGNC:16475]","synonyms":"SDR12C3","biotype":"protein_coding","ncbi_id":"83693","summary":null,"start":84122146,"end":84145192,"strand":-1,"description":"hydroxysteroid dehydrogenase like 1 [Source:HGNC Symbol;Acc:HGNC:16475]"}, {"versioned_ensembl_gene_id":"ENSG00000187988.5","gene_symbol":"KCTD9P3","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49912]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647013","summary":null,"start":37477149,"end":37478317,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49912]"}, {"versioned_ensembl_gene_id":"ENSG00000230662.1","gene_symbol":"TNPO1P2","gene_name":"transportin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45121]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"252968","summary":null,"start":18460391,"end":18463055,"strand":1,"description":"transportin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45121]"}, {"versioned_ensembl_gene_id":"ENSG00000230899.1","gene_symbol":"MAGEA8-AS1","gene_name":"MAGEA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45093]","synonyms":"RP5-869M20.2","biotype":"antisense_RNA","ncbi_id":"101410537","summary":null,"start":149878836,"end":149881070,"strand":-1,"description":"MAGEA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45093]"}, {"versioned_ensembl_gene_id":"ENSG00000213921.7","gene_symbol":"LEUTX","gene_name":"leucine twenty homeobox [Source:HGNC Symbol;Acc:HGNC:31953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342900","summary":null,"start":39776595,"end":39786167,"strand":1,"description":"leucine twenty homeobox [Source:HGNC Symbol;Acc:HGNC:31953]"}, {"versioned_ensembl_gene_id":"ENSG00000142544.6","gene_symbol":"CTU1","gene_name":"cytosolic thiouridylase subunit 1 [Source:HGNC Symbol;Acc:HGNC:29590]","synonyms":"NCS6,MGC17332,ATPBD3","biotype":"protein_coding","ncbi_id":"90353","summary":null,"start":51097606,"end":51108370,"strand":-1,"description":"cytosolic thiouridylase subunit 1 [Source:HGNC Symbol;Acc:HGNC:29590]"}, {"versioned_ensembl_gene_id":"ENSG00000278191.4","gene_symbol":"CARS","gene_name":"cysteinyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:1493]","synonyms":"CARS1","biotype":"protein_coding","ncbi_id":"833","summary":"This gene encodes a class 1 aminoacyl-tRNA synthetase, cysteinyl-tRNA synthetase. Each of the twenty aminoacyl-tRNA synthetases catalyzes the aminoacylation of a specific tRNA or tRNA isoaccepting family with the cognate amino acid. This gene is one of several located near the imprinted gene domain on chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":2999797,"end":3056458,"strand":-1,"description":"cysteinyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:1493]"}, {"versioned_ensembl_gene_id":"ENSG00000171116.7","gene_symbol":"HSFX1","gene_name":"heat shock transcription factor family, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:29603]","synonyms":"LW-1","biotype":"protein_coding","ncbi_id":"100506164","summary":null,"start":149774068,"end":149776867,"strand":1,"description":"heat shock transcription factor family, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:29603]"}, {"versioned_ensembl_gene_id":"ENSG00000173503.12","gene_symbol":"LTA","gene_name":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]","synonyms":"TNFB,LT,TNFSF1","biotype":"protein_coding","ncbi_id":"4049","summary":"The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":31562278,"end":31564550,"strand":1,"description":"lymphotoxin alpha [Source:HGNC Symbol;Acc:HGNC:6709]"}, {"versioned_ensembl_gene_id":"ENSG00000274993.1","gene_symbol":"AC254629.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100963828,"end":100968124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233942.1","gene_symbol":"AC004012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95471835,"end":95473998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011028.13","gene_symbol":"MRC2","gene_name":"mannose receptor C type 2 [Source:HGNC Symbol;Acc:HGNC:16875]","synonyms":"KIAA0709,ENDO180,CLEC13E,CD280","biotype":"protein_coding","ncbi_id":"9902","summary":"This gene encodes a member of the mannose receptor family of proteins that contain a fibronectin type II domain and multiple C-type lectin-like domains. The encoded protein plays a role in extracellular matrix remodeling by mediating the internalization and lysosomal degradation of collagen ligands. Expression of this gene may play a role in the tumorigenesis and metastasis of several malignancies including breast cancer, gliomas and metastatic bone disease. [provided by RefSeq, Feb 2012]","start":62627401,"end":62693597,"strand":1,"description":"mannose receptor C type 2 [Source:HGNC Symbol;Acc:HGNC:16875]"}, {"versioned_ensembl_gene_id":"ENSG00000274565.1","gene_symbol":"AC080038.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62626437,"end":62627590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271761.1","gene_symbol":"AL021368.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57902609,"end":57903148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234903.1","gene_symbol":"AC133104.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":95468863,"end":95469778,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108671.9","gene_symbol":"PSMD11","gene_name":"proteasome 26S subunit, non-ATPase 11 [Source:HGNC Symbol;Acc:HGNC:9556]","synonyms":"S9,Rpn6,p44.5,MGC3844","biotype":"protein_coding","ncbi_id":"5717","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the proteasome subunit S9 family that functions as a non-ATPase subunit of the 19S regulator and is phosphorylated by AMP-activated protein kinase. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":32444261,"end":32483318,"strand":1,"description":"proteasome 26S subunit, non-ATPase 11 [Source:HGNC Symbol;Acc:HGNC:9556]"}, {"versioned_ensembl_gene_id":"ENSG00000274455.1","gene_symbol":"AC092278.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":100062275,"end":100067954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258940.2","gene_symbol":"AL132639.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39265703,"end":39267061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233531.1","gene_symbol":"DEFA10P","gene_name":"defensin alpha 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:31801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"449493","summary":null,"start":6968141,"end":6969113,"strand":-1,"description":"defensin alpha 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:31801]"}, {"versioned_ensembl_gene_id":"ENSG00000090266.12","gene_symbol":"NDUFB2","gene_name":"NADH:ubiquinone oxidoreductase subunit B2 [Source:HGNC Symbol;Acc:HGNC:7697]","synonyms":"CI-AGGG,AGGG","biotype":"protein_coding","ncbi_id":"4708","summary":"The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It plays a important role in transfering electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Hydropathy analysis revealed that this subunit and 4 other subunits have an overall hydrophilic pattern, even though they are found within the hydrophobic protein (HP) fraction of complex I. [provided by RefSeq, Jul 2008]","start":140690777,"end":140722790,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B2 [Source:HGNC Symbol;Acc:HGNC:7697]"}, {"versioned_ensembl_gene_id":"ENSG00000267909.2","gene_symbol":"CCDC177","gene_name":"coiled-coil domain containing 177 [Source:HGNC Symbol;Acc:HGNC:23243]","synonyms":"C14orf162,PLPL","biotype":"protein_coding","ncbi_id":"56936","summary":null,"start":69569816,"end":69574837,"strand":-1,"description":"coiled-coil domain containing 177 [Source:HGNC Symbol;Acc:HGNC:23243]"}, {"versioned_ensembl_gene_id":"ENSG00000275893.1","gene_symbol":"AC008984.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54316929,"end":54345186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135540.11","gene_symbol":"NHSL1","gene_name":"NHS like 1 [Source:HGNC Symbol;Acc:HGNC:21021]","synonyms":"KIAA1357,C6orf63,bA43P8.1","biotype":"protein_coding","ncbi_id":"57224","summary":null,"start":138422043,"end":138692571,"strand":-1,"description":"NHS like 1 [Source:HGNC Symbol;Acc:HGNC:21021]"}, {"versioned_ensembl_gene_id":"ENSG00000180815.14","gene_symbol":"MAP3K15","gene_name":"mitogen-activated protein kinase kinase kinase 15 [Source:HGNC Symbol;Acc:HGNC:31689]","synonyms":"FLJ16518,bA723P2.3,ASK3","biotype":"protein_coding","ncbi_id":"389840","summary":"The protein encoded by this gene is a member of the mitogen-activated protein kinase (MAPK) family. These family members function in a protein kinase signal transduction cascade, where an activated MAPK kinase kinase (MAP3K) phosphorylates and activates a specific MAPK kinase (MAP2K), which then activates a specific MAPK. This MAP3K protein plays an essential role in apoptotic cell death triggered by cellular stresses. [provided by RefSeq, Jul 2010]","start":19360056,"end":19515261,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 15 [Source:HGNC Symbol;Acc:HGNC:31689]"}, {"versioned_ensembl_gene_id":"ENSG00000180938.5","gene_symbol":"ZNF572","gene_name":"zinc finger protein 572 [Source:HGNC Symbol;Acc:HGNC:26758]","synonyms":"FLJ38002","biotype":"protein_coding","ncbi_id":"137209","summary":null,"start":124973298,"end":124979389,"strand":1,"description":"zinc finger protein 572 [Source:HGNC Symbol;Acc:HGNC:26758]"}, {"versioned_ensembl_gene_id":"ENSG00000116903.7","gene_symbol":"EXOC8","gene_name":"exocyst complex component 8 [Source:HGNC Symbol;Acc:HGNC:24659]","synonyms":"SEC84,Exo84p,EXO84","biotype":"protein_coding","ncbi_id":"149371","summary":"This gene encodes a component of the exocyst complex, an evolutionarily conserved multi-protein complex that plays a critical role in vesicular trafficking and the secretory pathway by targeting post-Golgi vesicles to the plasma membrane. This protein is a target of activated Ral subfamily of GTPases and thereby regulates exocytosis by tethering vesicles to the plasma membrane. Mutations in this gene may be related to Joubert syndrome. [provided by RefSeq, Sep 2016]","start":231332753,"end":231337852,"strand":-1,"description":"exocyst complex component 8 [Source:HGNC Symbol;Acc:HGNC:24659]"}, {"versioned_ensembl_gene_id":"ENSG00000165244.6","gene_symbol":"ZNF367","gene_name":"zinc finger protein 367 [Source:HGNC Symbol;Acc:HGNC:18320]","synonyms":"FLJ33970","biotype":"protein_coding","ncbi_id":"195828","summary":null,"start":96385941,"end":96418329,"strand":-1,"description":"zinc finger protein 367 [Source:HGNC Symbol;Acc:HGNC:18320]"}, {"versioned_ensembl_gene_id":"ENSG00000250750.1","gene_symbol":"OR5BM1P","gene_name":"olfactory receptor family 5 subfamily BM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14835]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79491","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98053374,"end":98053739,"strand":1,"description":"olfactory receptor family 5 subfamily BM member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14835]"}, {"versioned_ensembl_gene_id":"ENSG00000274026.1","gene_symbol":"FAM27E3","gene_name":"family with sequence similarity 27 member E3 [Source:HGNC Symbol;Acc:HGNC:28655]","synonyms":"MGC42630","biotype":"transcribed_processed_pseudogene","ncbi_id":"100131997","summary":null,"start":67717411,"end":67719178,"strand":-1,"description":"family with sequence similarity 27 member E3 [Source:HGNC Symbol;Acc:HGNC:28655]"}, {"versioned_ensembl_gene_id":"ENSG00000184967.6","gene_symbol":"NOC4L","gene_name":"nucleolar complex associated 4 homolog [Source:HGNC Symbol;Acc:HGNC:28461]","synonyms":"UTP19,Noc4,NET49,MGC3162","biotype":"protein_coding","ncbi_id":"79050","summary":null,"start":132144448,"end":132152473,"strand":1,"description":"nucleolar complex associated 4 homolog [Source:HGNC Symbol;Acc:HGNC:28461]"}, {"versioned_ensembl_gene_id":"ENSG00000004455.16","gene_symbol":"AK2","gene_name":"adenylate kinase 2 [Source:HGNC Symbol;Acc:HGNC:362]","synonyms":null,"biotype":"protein_coding","ncbi_id":"204","summary":"Adenylate kinases are involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides. Three isozymes of adenylate kinase, namely 1, 2, and 3, have been identified in vertebrates; this gene encodes isozyme 2. Expression of these isozymes is tissue-specific and developmentally regulated. Isozyme 2 is localized in the mitochondrial intermembrane space and may play a role in apoptosis. Mutations in this gene are the cause of reticular dysgenesis. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 1 and 2.[provided by RefSeq, Nov 2010]","start":33007940,"end":33080996,"strand":-1,"description":"adenylate kinase 2 [Source:HGNC Symbol;Acc:HGNC:362]"}, {"versioned_ensembl_gene_id":"ENSG00000175344.17","gene_symbol":"CHRNA7","gene_name":"cholinergic receptor nicotinic alpha 7 subunit [Source:HGNC Symbol;Acc:HGNC:1960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1139","summary":"The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are thought to be hetero-pentamers composed of homologous subunits. The proposed structure for each subunit is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. The protein encoded by this gene forms a homo-oligomeric channel, displays marked permeability to calcium ions and is a major component of brain nicotinic receptors that are blocked by, and highly sensitive to, alpha-bungarotoxin. Once this receptor binds acetylcholine, it undergoes an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. This gene is located in a region identified as a major susceptibility locus for juvenile myoclonic epilepsy and a chromosomal location involved in the genetic transmission of schizophrenia. An evolutionarily recent partial duplication event in this region results in a hybrid containing sequence from this gene and a novel FAM7A gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":31923438,"end":32173018,"strand":1,"description":"cholinergic receptor nicotinic alpha 7 subunit [Source:HGNC Symbol;Acc:HGNC:1960]"}, {"versioned_ensembl_gene_id":"ENSG00000180539.7","gene_symbol":"C9orf139","gene_name":"chromosome 9 open reading frame 139 [Source:HGNC Symbol;Acc:HGNC:31426]","synonyms":"FLJ42909,FLJ36268","biotype":"antisense_RNA","ncbi_id":"401563","summary":null,"start":137027464,"end":137037957,"strand":1,"description":"chromosome 9 open reading frame 139 [Source:HGNC Symbol;Acc:HGNC:31426]"}, {"versioned_ensembl_gene_id":"ENSG00000131828.13","gene_symbol":"PDHA1","gene_name":"pyruvate dehydrogenase alpha 1 [Source:HGNC Symbol;Acc:HGNC:8806]","synonyms":"PDHA","biotype":"protein_coding","ncbi_id":"5160","summary":"The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 alpha 1 subunit containing the E1 active site, and plays a key role in the function of the PDH complex. Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]","start":19343893,"end":19361705,"strand":1,"description":"pyruvate dehydrogenase alpha 1 [Source:HGNC Symbol;Acc:HGNC:8806]"}, {"versioned_ensembl_gene_id":"ENSG00000106852.15","gene_symbol":"LHX6","gene_name":"LIM homeobox 6 [Source:HGNC Symbol;Acc:HGNC:21735]","synonyms":"LHX6.1","biotype":"protein_coding","ncbi_id":"26468","summary":"This gene encodes a member of a large protein family that contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein has tandem LIM domains as well as a DNA-binding homeodomain. The protein functions as a transcription factor involved in embryogenesis and head development and is highly expressed in neural crest derived mesenchyme cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2017]","start":122202577,"end":122229626,"strand":-1,"description":"LIM homeobox 6 [Source:HGNC Symbol;Acc:HGNC:21735]"}, {"versioned_ensembl_gene_id":"ENSG00000269460.1","gene_symbol":"AC005515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39685244,"end":39694577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264456.1","gene_symbol":"AC138207.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30971652,"end":30973312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236828.1","gene_symbol":"DMD-AS3","gene_name":"DMD antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40185]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873916","summary":null,"start":32754940,"end":32756400,"strand":1,"description":"DMD antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40185]"}, {"versioned_ensembl_gene_id":"ENSG00000283166.1","gene_symbol":"AL590396.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":237941452,"end":237942492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250999.1","gene_symbol":"AC136604.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179657762,"end":179664432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271086.5","gene_symbol":"NAMA","gene_name":"non-protein coding RNA, associated with MAP kinase pathway and growth arrest [Source:NCBI gene;Acc:100996569]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996569","summary":null,"start":99355337,"end":99377240,"strand":-1,"description":"non-protein coding RNA, associated with MAP kinase pathway and growth arrest [Source:NCBI gene;Acc:100996569]"}, {"versioned_ensembl_gene_id":"ENSG00000049089.13","gene_symbol":"COL9A2","gene_name":"collagen type IX alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2218]","synonyms":"MED,EDM2","biotype":"protein_coding","ncbi_id":"1298","summary":"This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. This chain is unusual in that, unlike the other two type IX alpha chains, it contains a covalently attached glycosaminoglycan side chain. Mutations in this gene are associated with multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008]","start":40300487,"end":40317816,"strand":-1,"description":"collagen type IX alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2218]"}, {"versioned_ensembl_gene_id":"ENSG00000267419.2","gene_symbol":"AC011477.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19776602,"end":19836073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203886.4","gene_symbol":"CYP17A1-AS1","gene_name":"CYP17A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31671]","synonyms":"CYP17A1OS,bA753C18.3","biotype":"antisense_RNA","ncbi_id":"102724307","summary":null,"start":102832721,"end":102834516,"strand":1,"description":"CYP17A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31671]"}, {"versioned_ensembl_gene_id":"ENSG00000237250.3","gene_symbol":"AL359924.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":237862175,"end":237928321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236081.1","gene_symbol":"ELFN1-AS1","gene_name":"ELFN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39071]","synonyms":"MYCLo-2","biotype":"lincRNA","ncbi_id":"101927125","summary":null,"start":1738630,"end":1742291,"strand":-1,"description":"ELFN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39071]"}, {"versioned_ensembl_gene_id":"ENSG00000224190.1","gene_symbol":"AL355537.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128912879,"end":128916271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204661.9","gene_symbol":"C5orf60","gene_name":"chromosome 5 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:27753]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285679","summary":null,"start":179641544,"end":179645046,"strand":-1,"description":"chromosome 5 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:27753]"}, {"versioned_ensembl_gene_id":"ENSG00000167588.12","gene_symbol":"GPD1","gene_name":"glycerol-3-phosphate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:4455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2819","summary":"This gene encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that facilitates the transfer of reducing equivalents from the cytosol to mitochondria. Mutations in this gene are a cause of transient infantile hypertriglyceridemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":50103819,"end":50111319,"strand":1,"description":"glycerol-3-phosphate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:4455]"}, {"versioned_ensembl_gene_id":"ENSG00000239527.1","gene_symbol":"RPS23P7","gene_name":"ribosomal protein S23 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43899]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130106","summary":null,"start":62397397,"end":62398142,"strand":1,"description":"ribosomal protein S23 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43899]"}, {"versioned_ensembl_gene_id":"ENSG00000223485.2","gene_symbol":"LINC01615","gene_name":"long intergenic non-protein coding RNA 1615 [Source:HGNC Symbol;Acc:HGNC:51898]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929484","summary":null,"start":169158092,"end":169162924,"strand":-1,"description":"long intergenic non-protein coding RNA 1615 [Source:HGNC Symbol;Acc:HGNC:51898]"}, {"versioned_ensembl_gene_id":"ENSG00000171368.11","gene_symbol":"TPPP","gene_name":"tubulin polymerization promoting protein [Source:HGNC Symbol;Acc:HGNC:24164]","synonyms":"TPPP1,TPPP/p25,p25alpha,p25","biotype":"protein_coding","ncbi_id":"11076","summary":null,"start":659862,"end":693395,"strand":-1,"description":"tubulin polymerization promoting protein [Source:HGNC Symbol;Acc:HGNC:24164]"}, {"versioned_ensembl_gene_id":"ENSG00000120708.16","gene_symbol":"TGFBI","gene_name":"transforming growth factor beta induced [Source:HGNC Symbol;Acc:HGNC:11771]","synonyms":"LCD1,CSD3,CSD2,CSD1,CDGG1,CDB1,BIGH3","biotype":"protein_coding","ncbi_id":"7045","summary":"This gene encodes an RGD-containing protein that binds to type I, II and IV collagens. The RGD motif is found in many extracellular matrix proteins modulating cell adhesion and serves as a ligand recognition sequence for several integrins. This protein plays a role in cell-collagen interactions and may be involved in endochondrial bone formation in cartilage. The protein is induced by transforming growth factor-beta and acts to inhibit cell adhesion. Mutations in this gene are associated with multiple types of corneal dystrophy. [provided by RefSeq, Jul 2008]","start":136028895,"end":136063818,"strand":1,"description":"transforming growth factor beta induced [Source:HGNC Symbol;Acc:HGNC:11771]"}, {"versioned_ensembl_gene_id":"ENSG00000242123.1","gene_symbol":"AC053481.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62319884,"end":62320189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216616.1","gene_symbol":"AL356421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47752828,"end":47753240,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264932.3","gene_symbol":"AC115989.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19649373,"end":19649935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100603.13","gene_symbol":"SNW1","gene_name":"SNW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16696]","synonyms":"SKIP1,SKIP,SKIIP,PRPF45,Prp45,NCoA-62,FUN20,Bx42","biotype":"protein_coding","ncbi_id":"22938","summary":"This gene, a member of the SNW gene family, encodes a coactivator that enhances transcription from some Pol II promoters. This coactivator can bind to the ligand-binding domain of the vitamin D receptor and to retinoid receptors to enhance vitamin D-, retinoic acid-, estrogen-, and glucocorticoid-mediated gene expression. It can also function as a splicing factor by interacting with poly(A)-binding protein 2 to directly control the expression of muscle-specific genes at the transcriptional level. Finally, the protein may be involved in oncogenesis since it interacts with a region of SKI oncoproteins that is required for transforming activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":77717599,"end":77761207,"strand":-1,"description":"SNW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16696]"}, {"versioned_ensembl_gene_id":"ENSG00000214788.2","gene_symbol":"OOSP1","gene_name":"oocyte secreted protein 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:49233]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"255649","summary":null,"start":59938455,"end":59995845,"strand":1,"description":"oocyte secreted protein 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:49233]"}, {"versioned_ensembl_gene_id":"ENSG00000107331.16","gene_symbol":"ABCA2","gene_name":"ATP binding cassette subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:32]","synonyms":"ABC2","biotype":"protein_coding","ncbi_id":"20","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This protein is highly expressed in brain tissue and may play a role in macrophage lipid metabolism and neural development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":137007227,"end":137028922,"strand":-1,"description":"ATP binding cassette subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:32]"}, {"versioned_ensembl_gene_id":"ENSG00000268603.1","gene_symbol":"AC053503.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219497611,"end":219498246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237461.1","gene_symbol":"AL359710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99585786,"end":99819889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164821.4","gene_symbol":"DEFA4","gene_name":"defensin alpha 4 [Source:HGNC Symbol;Acc:HGNC:2763]","synonyms":"DEF4,HP-4","biotype":"protein_coding","ncbi_id":"1669","summary":"Defensins are a family of antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules of neutrophils and also found in the epithelia of mucosal surfaces such as those of the intestine, respiratory tract, urinary tract, and vagina. Members of the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. Several alpha defensin genes are clustered on chromosome 8. This gene differs from other genes of this family by an extra 83-base segment that is apparently the result of a recent duplication within the coding region. The protein encoded by this gene, defensin, alpha 4, is found in the neutrophils; it exhibits corticostatic activity and inhibits corticotropin stimulated corticosterone production. [provided by RefSeq, Oct 2014]","start":6935822,"end":6938338,"strand":-1,"description":"defensin alpha 4 [Source:HGNC Symbol;Acc:HGNC:2763]"}, {"versioned_ensembl_gene_id":"ENSG00000258484.3","gene_symbol":"SPESP1","gene_name":"sperm equatorial segment protein 1 [Source:HGNC Symbol;Acc:HGNC:15570]","synonyms":"SP-ESP","biotype":"protein_coding","ncbi_id":"246777","summary":"The encoded protein is a human alloantigen involved in sperm-egg binding and fusion. [provided by RefSeq, Apr 2010]","start":68818221,"end":68946811,"strand":1,"description":"sperm equatorial segment protein 1 [Source:HGNC Symbol;Acc:HGNC:15570]"}, {"versioned_ensembl_gene_id":"ENSG00000260811.1","gene_symbol":"OR4C45","gene_name":"olfactory receptor family 4 subfamily C member 45 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:31270]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"403257","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":50032874,"end":50033794,"strand":1,"description":"olfactory receptor family 4 subfamily C member 45 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:31270]"}, {"versioned_ensembl_gene_id":"ENSG00000259286.3","gene_symbol":"AC087639.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68833830,"end":68834749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218265.1","gene_symbol":"RPS4XP7","gene_name":"ribosomal protein S4X pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36885]","synonyms":"RPS4P7","biotype":"processed_pseudogene","ncbi_id":"442162","summary":null,"start":13521266,"end":13522045,"strand":1,"description":"ribosomal protein S4X pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36885]"}, {"versioned_ensembl_gene_id":"ENSG00000234777.1","gene_symbol":"LINC02529","gene_name":"long intergenic non-protein coding RNA 2529 [Source:HGNC Symbol;Acc:HGNC:53555]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724053","summary":null,"start":159383531,"end":159396443,"strand":1,"description":"long intergenic non-protein coding RNA 2529 [Source:HGNC Symbol;Acc:HGNC:53555]"}, {"versioned_ensembl_gene_id":"ENSG00000278864.1","gene_symbol":"AC055811.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17181504,"end":17183257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224680.4","gene_symbol":"PLA2G12AP1","gene_name":"phospholipase A2 group XIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420258","summary":null,"start":52368677,"end":52369244,"strand":1,"description":"phospholipase A2 group XIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39248]"}, {"versioned_ensembl_gene_id":"ENSG00000253971.1","gene_symbol":"CDC42P3","gene_name":"cell division cycle 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44427]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128627","summary":null,"start":142995850,"end":142996482,"strand":1,"description":"cell division cycle 42 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44427]"}, {"versioned_ensembl_gene_id":"ENSG00000186831.11","gene_symbol":"KRT17P2","gene_name":"keratin 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6429]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339241","summary":null,"start":18426861,"end":18431848,"strand":1,"description":"keratin 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6429]"}, {"versioned_ensembl_gene_id":"ENSG00000091831.23","gene_symbol":"ESR1","gene_name":"estrogen receptor 1 [Source:HGNC Symbol;Acc:HGNC:3467]","synonyms":"NR3A1,ESR,Era","biotype":"protein_coding","ncbi_id":"2099","summary":"This gene encodes an estrogen receptor and ligand-activated transcription factor. The canonical protein contains an N-terminal ligand-independent transactivation domain, a central DNA binding domain, a hinge domain, and a C-terminal ligand-dependent transactivation domain. The protein localizes to the nucleus where it may form either a homodimer or a heterodimer with estrogen receptor 2. The protein encoded by this gene regulates the transcription of many estrogen-inducible genes that play a role in growth, metabolism, sexual development, gestation, and other reproductive functions and is expressed in many non-reproductive tissues. The receptor encoded by this gene plays a key role in breast cancer, endometrial cancer, and osteoporosis. This gene is reported to have dozens of transcript variants due to the use of alternate promoters and alternative splicing, however, the full-length nature of many of these variants remain uncertain. [provided by RefSeq, Jul 2020]","start":151656691,"end":152129619,"strand":1,"description":"estrogen receptor 1 [Source:HGNC Symbol;Acc:HGNC:3467]"}, {"versioned_ensembl_gene_id":"ENSG00000234577.1","gene_symbol":"SYNE1-AS1","gene_name":"SYNE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40793]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505475","summary":null,"start":152380546,"end":152381564,"strand":1,"description":"SYNE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40793]"}, {"versioned_ensembl_gene_id":"ENSG00000271499.1","gene_symbol":"AC011477.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19750618,"end":19752544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282523.1","gene_symbol":"AC243807.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45743300,"end":45744574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282361.1","gene_symbol":"AC243807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45744950,"end":45746266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276046.1","gene_symbol":"DUX4L13","gene_name":"double homeobox 4 like 13 [Source:HGNC Symbol;Acc:HGNC:38672]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100289581","summary":null,"start":133753250,"end":133754516,"strand":1,"description":"double homeobox 4 like 13 [Source:HGNC Symbol;Acc:HGNC:38672]"}, {"versioned_ensembl_gene_id":"ENSG00000105708.8","gene_symbol":"ZNF14","gene_name":"zinc finger protein 14 [Source:HGNC Symbol;Acc:HGNC:12924]","synonyms":"KOX6,GIOT-4","biotype":"protein_coding","ncbi_id":"7561","summary":"The protein encoded by this gene contains a zinc finger and a Kruppel-associated box (KRAB) domain. KRAB domain is known to be involved in the transcriptional repression of a number of zinc finger proteins. [provided by RefSeq, Jul 2008]","start":19710471,"end":19733097,"strand":-1,"description":"zinc finger protein 14 [Source:HGNC Symbol;Acc:HGNC:12924]"}, {"versioned_ensembl_gene_id":"ENSG00000253559.1","gene_symbol":"OSGEPL1-AS1","gene_name":"OSGEPL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41009]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101409258","summary":null,"start":189762704,"end":189765556,"strand":1,"description":"OSGEPL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41009]"}, {"versioned_ensembl_gene_id":"ENSG00000254727.1","gene_symbol":"PTP4A1P6","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:41933]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100129472","summary":null,"start":86432098,"end":86432575,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:41933]"}, {"versioned_ensembl_gene_id":"ENSG00000151376.16","gene_symbol":"ME3","gene_name":"malic enzyme 3 [Source:HGNC Symbol;Acc:HGNC:6985]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10873","summary":"Malic enzyme catalyzes the oxidative decarboxylation of malate to pyruvate using either NAD+ or NADP+ as a cofactor. Mammalian tissues contain 3 distinct isoforms of malic enzyme: a cytosolic NADP(+)-dependent isoform, a mitochondrial NADP(+)-dependent isoform, and a mitochondrial NAD(+)-dependent isoform. This gene encodes a mitochondrial NADP(+)-dependent isoform. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":86441108,"end":86672636,"strand":-1,"description":"malic enzyme 3 [Source:HGNC Symbol;Acc:HGNC:6985]"}, {"versioned_ensembl_gene_id":"ENSG00000227474.1","gene_symbol":"RPL6P24","gene_name":"ribosomal protein L6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271034","summary":null,"start":13591460,"end":13592323,"strand":-1,"description":"ribosomal protein L6 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36343]"}, {"versioned_ensembl_gene_id":"ENSG00000088826.17","gene_symbol":"SMOX","gene_name":"spermine oxidase [Source:HGNC Symbol;Acc:HGNC:15862]","synonyms":"C20orf16,SMO,PAOh1,PAO,MGC1010,FLJ20746,dJ779E11.1","biotype":"protein_coding","ncbi_id":"54498","summary":"Polyamines are ubiquitous polycationic alkylamines which include spermine, spermidine, putrescine, and agmatine. These molecules participate in a broad range of cellular functions which include cell cycle modulation, scavenging reactive oxygen species, and the control of gene expression. These molecules also play important roles in neurotransmission through their regulation of cell-surface receptor activity, involvement in intracellular signalling pathways, and their putative roles as neurotransmitters. This gene encodes an FAD-containing enzyme that catalyzes the oxidation of spermine to spermadine and secondarily produces hydrogen peroxide. Multiple transcript variants encoding different isoenzymes have been identified for this gene, some of which have failed to demonstrate significant oxidase activity on natural polyamine substrates. The characterized isoenzymes have distinctive biochemical characteristics and substrate specificities, suggesting the existence of additional levels of complexity in polyamine catabolism. [provided by RefSeq, Jul 2012]","start":4120980,"end":4187747,"strand":1,"description":"spermine oxidase [Source:HGNC Symbol;Acc:HGNC:15862]"}, {"versioned_ensembl_gene_id":"ENSG00000066651.18","gene_symbol":"TRMT11","gene_name":"tRNA methyltransferase 11 homolog [Source:HGNC Symbol;Acc:HGNC:21080]","synonyms":"TRMT11-1,TRM11,MDS024,dJ187J11.2,C6orf75","biotype":"protein_coding","ncbi_id":"60487","summary":null,"start":125986430,"end":126039276,"strand":1,"description":"tRNA methyltransferase 11 homolog [Source:HGNC Symbol;Acc:HGNC:21080]"}, {"versioned_ensembl_gene_id":"ENSG00000111536.4","gene_symbol":"IL26","gene_name":"interleukin 26 [Source:HGNC Symbol;Acc:HGNC:17119]","synonyms":"IL-26,AK155","biotype":"protein_coding","ncbi_id":"55801","summary":"This gene was identified by its overexpression specifically in herpesvirus samimiri-transformed T cells. The encoded protein is a member of the IL10 family of cytokines. It is a secreted protein and may function as a homodimer. This protein is thought to contribute to the transformed phenotype of T cells after infection by herpesvirus samimiri. [provided by RefSeq, Jul 2008]","start":68201351,"end":68225821,"strand":-1,"description":"interleukin 26 [Source:HGNC Symbol;Acc:HGNC:17119]"}, {"versioned_ensembl_gene_id":"ENSG00000139908.14","gene_symbol":"TSSK4","gene_name":"testis specific serine kinase 4 [Source:HGNC Symbol;Acc:HGNC:19825]","synonyms":"STK22E,C14orf20","biotype":"protein_coding","ncbi_id":"283629","summary":"This gene encodes a member of the testis-specific serine/threonine kinase family. The encoded protein is thought to be involved in spermatogenesis via stimulation of the CREB/CRE responsive pathway through phosphorylation of the cAMP responsive element binding protein transcription factor. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":24205697,"end":24208362,"strand":1,"description":"testis specific serine kinase 4 [Source:HGNC Symbol;Acc:HGNC:19825]"}, {"versioned_ensembl_gene_id":"ENSG00000205578.5","gene_symbol":"POM121B","gene_name":"POM121 transmembrane nucleoporin B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34004]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288540","summary":null,"start":73293497,"end":73301161,"strand":1,"description":"POM121 transmembrane nucleoporin B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34004]"}, {"versioned_ensembl_gene_id":"ENSG00000213920.8","gene_symbol":"MDP1","gene_name":"magnesium dependent phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28781]","synonyms":"FN6Pase,MGC5987","biotype":"protein_coding","ncbi_id":"145553","summary":null,"start":24213937,"end":24216070,"strand":-1,"description":"magnesium dependent phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28781]"}, {"versioned_ensembl_gene_id":"ENSG00000126947.12","gene_symbol":"ARMCX1","gene_name":"armadillo repeat containing, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:18073]","synonyms":"GASP7,ALEX1","biotype":"protein_coding","ncbi_id":"51309","summary":"This gene encodes a member of the ALEX family of proteins and may play a role in tumor suppression. The encoded protein contains a potential N-terminal transmembrane domain and two Armadillo (arm) repeats. Other proteins containing the arm repeat are involved in development, maintenance of tissue integrity, and tumorigenesis. This gene is closely localized with other family members, including ALEX2 and ALEX3, on the X chromosome. [provided by RefSeq, Jul 2008]","start":101550531,"end":101554700,"strand":1,"description":"armadillo repeat containing, X-linked 1 [Source:HGNC Symbol;Acc:HGNC:18073]"}, {"versioned_ensembl_gene_id":"ENSG00000185669.5","gene_symbol":"SNAI3","gene_name":"snail family transcriptional repressor 3 [Source:HGNC Symbol;Acc:HGNC:18411]","synonyms":"ZNF293,Zfp293,SMUC","biotype":"protein_coding","ncbi_id":"333929","summary":"SNAI3 is a member of the SNAIL gene family, named for the Drosophila snail gene, which plays roles in mesodermal formation during embryogenesis (Katoh and Katoh, 2003 [PubMed 12579345]).[supplied by OMIM, Apr 2009]","start":88677682,"end":88686493,"strand":-1,"description":"snail family transcriptional repressor 3 [Source:HGNC Symbol;Acc:HGNC:18411]"}, {"versioned_ensembl_gene_id":"ENSG00000187013.4","gene_symbol":"C17orf82","gene_name":"chromosome 17 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:32699]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388407","summary":null,"start":61411751,"end":61413280,"strand":1,"description":"chromosome 17 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:32699]"}, {"versioned_ensembl_gene_id":"ENSG00000164694.16","gene_symbol":"FNDC1","gene_name":"fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21184]","synonyms":"dJ322A24.1,bA243O10.1,KIAA1866,FNDC2","biotype":"protein_coding","ncbi_id":"84624","summary":null,"start":159169397,"end":159272109,"strand":1,"description":"fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21184]"}, {"versioned_ensembl_gene_id":"ENSG00000224292.1","gene_symbol":"AF196972.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48506523,"end":48508838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238098.9","gene_symbol":"ABCA17P","gene_name":"ATP binding cassette subfamily A member 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:32972]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"650655","summary":null,"start":2339150,"end":2426699,"strand":1,"description":"ATP binding cassette subfamily A member 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:32972]"}, {"versioned_ensembl_gene_id":"ENSG00000230391.1","gene_symbol":"RPSAP23","gene_name":"ribosomal protein SA pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270875","summary":null,"start":115468056,"end":115468938,"strand":1,"description":"ribosomal protein SA pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36742]"}, {"versioned_ensembl_gene_id":"ENSG00000255970.1","gene_symbol":"LINC02421","gene_name":"long intergenic non-protein coding RNA 2421 [Source:HGNC Symbol;Acc:HGNC:53351]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927901","summary":null,"start":67709047,"end":67729475,"strand":-1,"description":"long intergenic non-protein coding RNA 2421 [Source:HGNC Symbol;Acc:HGNC:53351]"}, {"versioned_ensembl_gene_id":"ENSG00000277423.1","gene_symbol":"AC069234.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120703867,"end":120704282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174238.14","gene_symbol":"PITPNA","gene_name":"phosphatidylinositol transfer protein alpha [Source:HGNC Symbol;Acc:HGNC:9001]","synonyms":"VIB1A,PITPN","biotype":"protein_coding","ncbi_id":"5306","summary":"This gene encodes a member of a family of lipid-binding proteins that transfer molecules of phosphatidylinositol or phosphatidylcholine between membrane surfaces. The protein is implicated in phospholipase C signaling and in the production of phosphatidylinositol 3,4,5-trisphosphate (PIP3) by phosphoinositide-3-kinase.[provided by RefSeq, Sep 2009]","start":1517718,"end":1562816,"strand":-1,"description":"phosphatidylinositol transfer protein alpha [Source:HGNC Symbol;Acc:HGNC:9001]"}, {"versioned_ensembl_gene_id":"ENSG00000176142.12","gene_symbol":"TMEM39A","gene_name":"transmembrane protein 39A [Source:HGNC Symbol;Acc:HGNC:25600]","synonyms":"FLJ10902","biotype":"protein_coding","ncbi_id":"55254","summary":null,"start":119429500,"end":119468830,"strand":-1,"description":"transmembrane protein 39A [Source:HGNC Symbol;Acc:HGNC:25600]"}, {"versioned_ensembl_gene_id":"ENSG00000145826.8","gene_symbol":"LECT2","gene_name":"leukocyte cell derived chemotaxin 2 [Source:HGNC Symbol;Acc:HGNC:6550]","synonyms":"chm2,chm-II","biotype":"protein_coding","ncbi_id":"3950","summary":"This gene encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth of chondrocytes and osteoblasts. This protein has high sequence similarity to the chondromodulin repeat regions of the chicken myb-induced myeloid 1 protein. A polymorphism in this gene may be associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]","start":135922279,"end":135955034,"strand":-1,"description":"leukocyte cell derived chemotaxin 2 [Source:HGNC Symbol;Acc:HGNC:6550]"}, {"versioned_ensembl_gene_id":"ENSG00000141198.15","gene_symbol":"TOM1L1","gene_name":"target of myb1 like 1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11983]","synonyms":"SRCASM","biotype":"protein_coding","ncbi_id":"10040","summary":null,"start":54899387,"end":54961956,"strand":1,"description":"target of myb1 like 1 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11983]"}, {"versioned_ensembl_gene_id":"ENSG00000135407.10","gene_symbol":"AVIL","gene_name":"advillin [Source:HGNC Symbol;Acc:HGNC:14188]","synonyms":"p92,FLJ12386,DOC6,ADVIL","biotype":"protein_coding","ncbi_id":"10677","summary":"The protein encoded by this gene is a member of the gelsolin/villin family of actin regulatory proteins. This protein has structural similarity to villin. It binds actin and may play a role in the development of neuronal cells that form ganglia. [provided by RefSeq, Jul 2008]","start":57797376,"end":57818704,"strand":-1,"description":"advillin [Source:HGNC Symbol;Acc:HGNC:14188]"}, {"versioned_ensembl_gene_id":"ENSG00000253940.1","gene_symbol":"AC026421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31065970,"end":31066132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142185.16","gene_symbol":"TRPM2","gene_name":"transient receptor potential cation channel subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:12339]","synonyms":"TRPC7,NUDT9L1,NUDT9H,LTRPC2,KNP3,EREG1","biotype":"protein_coding","ncbi_id":"7226","summary":"The protein encoded by this gene forms a tetrameric cation channel that is permeable to calcium, sodium, and potassium and is regulated by free intracellular ADP-ribose. The encoded protein is activated by oxidative stress and confers susceptibility to cell death. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. Additional transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2016]","start":44350163,"end":44443081,"strand":1,"description":"transient receptor potential cation channel subfamily M member 2 [Source:HGNC Symbol;Acc:HGNC:12339]"}, {"versioned_ensembl_gene_id":"ENSG00000280986.1","gene_symbol":"LINC01659","gene_name":"long intergenic non-protein coding RNA 1659 [Source:HGNC Symbol;Acc:HGNC:52447]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929374","summary":null,"start":23433564,"end":23435071,"strand":1,"description":"long intergenic non-protein coding RNA 1659 [Source:HGNC Symbol;Acc:HGNC:52447]"}, {"versioned_ensembl_gene_id":"ENSG00000083812.11","gene_symbol":"ZNF324","gene_name":"zinc finger protein 324 [Source:HGNC Symbol;Acc:HGNC:14096]","synonyms":"ZNF324A,ZF5128","biotype":"protein_coding","ncbi_id":"25799","summary":null,"start":58467045,"end":58475436,"strand":1,"description":"zinc finger protein 324 [Source:HGNC Symbol;Acc:HGNC:14096]"}, {"versioned_ensembl_gene_id":"ENSG00000095139.13","gene_symbol":"ARCN1","gene_name":"archain 1 [Source:HGNC Symbol;Acc:HGNC:649]","synonyms":"COPD","biotype":"protein_coding","ncbi_id":"372","summary":"This gene maps in a region, which include the mixed lineage leukemia and Friend leukemia virus integration 1 genes, where multiple disease-associated chromosome translocations occur. It is an intracellular protein. Archain sequences are well conserved among eukaryotes and this protein may play a fundamental role in eukaryotic cell biology. It has similarities to heat shock proteins and clathrin-associated proteins, and may be involved in vesicle structure or trafficking. [provided by RefSeq, Jul 2008]","start":118572390,"end":118603033,"strand":1,"description":"archain 1 [Source:HGNC Symbol;Acc:HGNC:649]"}, {"versioned_ensembl_gene_id":"ENSG00000276644.4","gene_symbol":"DACH1","gene_name":"dachshund family transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:2663]","synonyms":"DACH","biotype":"protein_coding","ncbi_id":"1602","summary":"This gene encodes a chromatin-associated protein that associates with other DNA-binding transcription factors to regulate gene expression and cell fate determination during development. The protein contains a Ski domain that is highly conserved from Drosophila to human. Expression of this gene is lost in some forms of metastatic cancer, and is correlated with poor prognosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":71437966,"end":71867192,"strand":-1,"description":"dachshund family transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:2663]"}, {"versioned_ensembl_gene_id":"ENSG00000213467.4","gene_symbol":"HMGB1P37","gene_name":"high mobility group box 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39184]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132863","summary":null,"start":121519816,"end":121520424,"strand":-1,"description":"high mobility group box 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39184]"}, {"versioned_ensembl_gene_id":"ENSG00000265799.1","gene_symbol":"AC090844.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40012226,"end":40014705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275894.1","gene_symbol":"AL021578.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45345115,"end":45345823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255833.1","gene_symbol":"TIFAB","gene_name":"TIFA inhibitor [Source:HGNC Symbol;Acc:HGNC:34024]","synonyms":null,"biotype":"protein_coding","ncbi_id":"497189","summary":"TIFAB associates with TIFA (MIM 609028) and inhibits TIFA-mediated activation of NF-kappa-B (NFKB1; MIM 164011) (Matsumura et al., 2004 [PubMed 15047173]).[supplied by OMIM, Mar 2009]","start":135444218,"end":135452399,"strand":-1,"description":"TIFA inhibitor [Source:HGNC Symbol;Acc:HGNC:34024]"}, {"versioned_ensembl_gene_id":"ENSG00000168993.14","gene_symbol":"CPLX1","gene_name":"complexin 1 [Source:HGNC Symbol;Acc:HGNC:2309]","synonyms":"CPX-I","biotype":"protein_coding","ncbi_id":"10815","summary":"Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the SNAP receptor complex and disrupts it, allowing transmitter release. [provided by RefSeq, Jul 2008]","start":784957,"end":826198,"strand":-1,"description":"complexin 1 [Source:HGNC Symbol;Acc:HGNC:2309]"}, {"versioned_ensembl_gene_id":"ENSG00000284341.1","gene_symbol":"AL807752.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":136977518,"end":136985435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223470.3","gene_symbol":"AL117338.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33909238,"end":33917804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262518.1","gene_symbol":"AC090079.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53438556,"end":53439721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250118.1","gene_symbol":"AC114300.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30365405,"end":30365684,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262271.1","gene_symbol":"AC090079.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53434131,"end":53435829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213045.3","gene_symbol":"AC097065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":200329161,"end":200329677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232892.1","gene_symbol":"AL499616.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":163161675,"end":163213023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225079.2","gene_symbol":"FTH1P22","gene_name":"ferritin heavy chain 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37640]","synonyms":"FTHL22","biotype":"processed_pseudogene","ncbi_id":"100462772","summary":null,"start":116775104,"end":116775623,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37640]"}, {"versioned_ensembl_gene_id":"ENSG00000162819.11","gene_symbol":"BROX","gene_name":"BRO1 domain and CAAX motif containing [Source:HGNC Symbol;Acc:HGNC:26512]","synonyms":"FLJ32421,C1orf58","biotype":"protein_coding","ncbi_id":"148362","summary":null,"start":222712553,"end":222735196,"strand":1,"description":"BRO1 domain and CAAX motif containing [Source:HGNC Symbol;Acc:HGNC:26512]"}, {"versioned_ensembl_gene_id":"ENSG00000229399.1","gene_symbol":"AL592148.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":222641414,"end":222641858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226916.8","gene_symbol":"WDR46","gene_name":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]","synonyms":"BING4,UTP7,C6orf11","biotype":"protein_coding","ncbi_id":"9277","summary":null,"start":33257029,"end":33267452,"strand":-1,"description":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]"}, {"versioned_ensembl_gene_id":"ENSG00000240870.2","gene_symbol":"AP003551.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98782055,"end":98782628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068438.14","gene_symbol":"FTSJ1","gene_name":"FtsJ RNA methyltransferase homolog 1 (E. coli) [Source:HGNC Symbol;Acc:HGNC:13254]","synonyms":"TRMT7,TRM7,SPB1,MRX9,MRX44,JM23,CDLIV","biotype":"protein_coding","ncbi_id":"24140","summary":"This gene encodes a member of the methyltransferase superfamily. The encoded protein localizes to the nucleolus, binds to S-adenosylmethionine, and may be involved in the processing and modification of ribosomal RNA. Mutations in this gene are associated with cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":48476021,"end":48486364,"strand":1,"description":"FtsJ RNA methyltransferase homolog 1 (E. coli) [Source:HGNC Symbol;Acc:HGNC:13254]"}, {"versioned_ensembl_gene_id":"ENSG00000237808.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31576297,"end":31580387,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000244383.1","gene_symbol":"FAM3D-AS1","gene_name":"FAM3D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41276]","synonyms":"lnc-KCTD6-3","biotype":"antisense_RNA","ncbi_id":"105377108","summary":null,"start":58607080,"end":58634440,"strand":1,"description":"FAM3D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41276]"}, {"versioned_ensembl_gene_id":"ENSG00000228190.2","gene_symbol":"RPL23AP16","gene_name":"ribosomal protein L23a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36652]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647201","summary":null,"start":199371877,"end":199372297,"strand":1,"description":"ribosomal protein L23a pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36652]"}, {"versioned_ensembl_gene_id":"ENSG00000236468.1","gene_symbol":"AC099335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199387141,"end":199388475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055813.5","gene_symbol":"CCDC85A","gene_name":"coiled-coil domain containing 85A [Source:HGNC Symbol;Acc:HGNC:29400]","synonyms":"KIAA1912","biotype":"protein_coding","ncbi_id":"114800","summary":null,"start":56184123,"end":56386173,"strand":1,"description":"coiled-coil domain containing 85A [Source:HGNC Symbol;Acc:HGNC:29400]"}, {"versioned_ensembl_gene_id":"ENSG00000241950.1","gene_symbol":"RPL29P23","gene_name":"ribosomal protein L29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646077","summary":null,"start":33190062,"end":33190503,"strand":-1,"description":"ribosomal protein L29 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:35946]"}, {"versioned_ensembl_gene_id":"ENSG00000258193.1","gene_symbol":"AC011602.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81998632,"end":81998962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280555.2","gene_symbol":"LINC02203","gene_name":"long intergenic non-protein coding RNA 2203 [Source:HGNC Symbol;Acc:HGNC:53069]","synonyms":null,"biotype":"lincRNA","ncbi_id":"727924","summary":null,"start":21552724,"end":21660461,"strand":1,"description":"long intergenic non-protein coding RNA 2203 [Source:HGNC Symbol;Acc:HGNC:53069]"}, {"versioned_ensembl_gene_id":"ENSG00000230289.1","gene_symbol":"AL358781.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131516558,"end":131522229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261831.2","gene_symbol":"AL353708.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179926641,"end":179941796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260360.1","gene_symbol":"AL353708.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179953184,"end":179954440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152208.12","gene_symbol":"GRID2","gene_name":"glutamate ionotropic receptor delta type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4576]","synonyms":"GluR-delta-2,GluD2","biotype":"protein_coding","ncbi_id":"2895","summary":"The protein encoded by this gene is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans. [provided by RefSeq, Apr 2014]","start":92303622,"end":93810157,"strand":1,"description":"glutamate ionotropic receptor delta type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4576]"}, {"versioned_ensembl_gene_id":"ENSG00000006282.20","gene_symbol":"SPATA20","gene_name":"spermatogenesis associated 20 [Source:HGNC Symbol;Acc:HGNC:26125]","synonyms":"Tisp78,SSP411,FLJ21347","biotype":"protein_coding","ncbi_id":"64847","summary":null,"start":50543058,"end":50555852,"strand":1,"description":"spermatogenesis associated 20 [Source:HGNC Symbol;Acc:HGNC:26125]"}, {"versioned_ensembl_gene_id":"ENSG00000229435.2","gene_symbol":"PIP5K1P2","gene_name":"phosphatidylinositol-4-phosphate 5-kinase type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38068]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129824","summary":null,"start":159231435,"end":159233377,"strand":1,"description":"phosphatidylinositol-4-phosphate 5-kinase type 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38068]"}, {"versioned_ensembl_gene_id":"ENSG00000249351.2","gene_symbol":"AC096754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65216616,"end":65217433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152689.17","gene_symbol":"RASGRP3","gene_name":"RAS guanyl releasing protein 3 [Source:HGNC Symbol;Acc:HGNC:14545]","synonyms":"KIAA0846,GRP3,CalDAG-GEFIII","biotype":"protein_coding","ncbi_id":"25780","summary":"The protein encoded by this gene is a guanine nucleotide exchange factor that activates the oncogenes HRAS and RAP1A. Defects in this gene have been associated with systemic lupus erythematosus and several cancers. [provided by RefSeq, Mar 2017]","start":33436324,"end":33564750,"strand":1,"description":"RAS guanyl releasing protein 3 [Source:HGNC Symbol;Acc:HGNC:14545]"}, {"versioned_ensembl_gene_id":"ENSG00000142494.13","gene_symbol":"SLC47A1","gene_name":"solute carrier family 47 member 1 [Source:HGNC Symbol;Acc:HGNC:25588]","synonyms":"MATE1,FLJ10847","biotype":"protein_coding","ncbi_id":"55244","summary":"This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]","start":19495385,"end":19579034,"strand":1,"description":"solute carrier family 47 member 1 [Source:HGNC Symbol;Acc:HGNC:25588]"}, {"versioned_ensembl_gene_id":"ENSG00000253806.1","gene_symbol":"AC108002.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142727283,"end":142727690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251389.1","gene_symbol":"YTHDF1P1","gene_name":"YTH domain family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31681]","synonyms":"YTHDF1P","biotype":"processed_pseudogene","ncbi_id":"402220","summary":null,"start":97368776,"end":97370421,"strand":1,"description":"YTH domain family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31681]"}, {"versioned_ensembl_gene_id":"ENSG00000205869.2","gene_symbol":"KRTAP5-1","gene_name":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]","synonyms":"KRTAP5.1,KRN1L","biotype":"protein_coding","ncbi_id":"387264","summary":null,"start":1584342,"end":1585283,"strand":-1,"description":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]"}, {"versioned_ensembl_gene_id":"ENSG00000188778.5","gene_symbol":"ADRB3","gene_name":"adrenoceptor beta 3 [Source:HGNC Symbol;Acc:HGNC:288]","synonyms":null,"biotype":"protein_coding","ncbi_id":"155","summary":"The protein encoded by this gene belongs to the family of beta adrenergic receptors, which mediate catecholamine-induced activation of adenylate cyclase through the action of G proteins. This receptor is located mainly in the adipose tissue and is involved in the regulation of lipolysis and thermogenesis. Obesity and bodyweight-related disorders are correlated with certain polymorphisms in three subtypes of beta-adrenoceptor, among them, the ADRB3 gene.[provided by RefSeq, Oct 2019]","start":37962991,"end":37966965,"strand":-1,"description":"adrenoceptor beta 3 [Source:HGNC Symbol;Acc:HGNC:288]"}, {"versioned_ensembl_gene_id":"ENSG00000254699.1","gene_symbol":"AP003097.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86192787,"end":86193482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166884.2","gene_symbol":"OR4D6","gene_name":"olfactory receptor family 4 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:15175]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219983","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59456938,"end":59457991,"strand":1,"description":"olfactory receptor family 4 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:15175]"}, {"versioned_ensembl_gene_id":"ENSG00000150361.11","gene_symbol":"KLHL1","gene_name":"kelch like family member 1 [Source:HGNC Symbol;Acc:HGNC:6352]","synonyms":"FLJ30047,MRP2,KIAA1490","biotype":"protein_coding","ncbi_id":"57626","summary":"The KLHL1 protein belongs to a family of actin-organizing proteins related to Drosophila Kelch (Nemes et al., 2000 [PubMed 10888605]).[supplied by OMIM, Feb 2010]","start":69700594,"end":70108493,"strand":-1,"description":"kelch like family member 1 [Source:HGNC Symbol;Acc:HGNC:6352]"}, {"versioned_ensembl_gene_id":"ENSG00000110344.9","gene_symbol":"UBE4A","gene_name":"ubiquitination factor E4A [Source:HGNC Symbol;Acc:HGNC:12499]","synonyms":"UFD2,UBOX2,KIAA0126,E4","biotype":"protein_coding","ncbi_id":"9354","summary":"This gene encodes a member of the U-box ubiquitin ligase family. The encoded protein is involved in multiubiquitin chain assembly and plays a critical role in chromosome condensation and separation through the polyubiquitination of securin. Autoantibodies against the encoded protein may be markers for scleroderma and Crohn's disease. A pseudogene of this gene is located on the long arm of chromosome 3. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]","start":118359585,"end":118399211,"strand":1,"description":"ubiquitination factor E4A [Source:HGNC Symbol;Acc:HGNC:12499]"}, {"versioned_ensembl_gene_id":"ENSG00000187193.8","gene_symbol":"MT1X","gene_name":"metallothionein 1X [Source:HGNC Symbol;Acc:HGNC:7405]","synonyms":"MT1,MT-1l","biotype":"protein_coding","ncbi_id":"4501","summary":null,"start":56682424,"end":56684196,"strand":1,"description":"metallothionein 1X [Source:HGNC Symbol;Acc:HGNC:7405]"}, {"versioned_ensembl_gene_id":"ENSG00000230268.3","gene_symbol":"SSU72P8","gene_name":"SSU72 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43627]","synonyms":null,"biotype":"protein_coding","ncbi_id":"136157","summary":null,"start":124476371,"end":124476955,"strand":1,"description":"SSU72 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43627]"}, {"versioned_ensembl_gene_id":"ENSG00000143028.8","gene_symbol":"SYPL2","gene_name":"synaptophysin like 2 [Source:HGNC Symbol;Acc:HGNC:27638]","synonyms":"Mg29","biotype":"protein_coding","ncbi_id":"284612","summary":null,"start":109466628,"end":109482137,"strand":1,"description":"synaptophysin like 2 [Source:HGNC Symbol;Acc:HGNC:27638]"}, {"versioned_ensembl_gene_id":"ENSG00000265094.1","gene_symbol":"AC007922.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24435364,"end":24439638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179615.2","gene_symbol":"OR2AP1","gene_name":"olfactory receptor family 2 subfamily AP member 1 [Source:HGNC Symbol;Acc:HGNC:15335]","synonyms":"OR2AP1P","biotype":"protein_coding","ncbi_id":"121129","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55572468,"end":55575612,"strand":1,"description":"olfactory receptor family 2 subfamily AP member 1 [Source:HGNC Symbol;Acc:HGNC:15335]"}, {"versioned_ensembl_gene_id":"ENSG00000225536.2","gene_symbol":"STIP1P3","gene_name":"stress induced phosphoprotein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441505","summary":null,"start":86084716,"end":86086339,"strand":-1,"description":"stress induced phosphoprotein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49554]"}, {"versioned_ensembl_gene_id":"ENSG00000254536.1","gene_symbol":"AL360181.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":133390834,"end":133420495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242262.1","gene_symbol":"AC092597.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47706372,"end":47706987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254567.2","gene_symbol":"UBTFL9","gene_name":"upstream binding transcription factor, RNA polymerase I-like 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50286]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128427","summary":null,"start":49133653,"end":49134800,"strand":-1,"description":"upstream binding transcription factor, RNA polymerase I-like 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:50286]"}, {"versioned_ensembl_gene_id":"ENSG00000238019.1","gene_symbol":"AL360169.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158397885,"end":158398561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181472.4","gene_symbol":"ZBTB2","gene_name":"zinc finger and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20868]","synonyms":"ZNF437,KIAA1483,bA351K16.2","biotype":"protein_coding","ncbi_id":"57621","summary":null,"start":151364117,"end":151391548,"strand":-1,"description":"zinc finger and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20868]"}, {"versioned_ensembl_gene_id":"ENSG00000228207.1","gene_symbol":"AC007967.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8901203,"end":8903276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005513.9","gene_symbol":"SOX8","gene_name":"SRY-box 8 [Source:HGNC Symbol;Acc:HGNC:11203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30812","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the cognitive disability found in an alpha-thalassemia-related syndrome (ART-16). This protein is also highly expressed in the majority of human hepatocellular carcinomas and promotes cellular proliferation and enhanced tumor growth. [provided by RefSeq, Jul 2017]","start":981808,"end":986979,"strand":1,"description":"SRY-box 8 [Source:HGNC Symbol;Acc:HGNC:11203]"}, {"versioned_ensembl_gene_id":"ENSG00000183911.7","gene_symbol":"RPL21P132","gene_name":"ribosomal protein L21 pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:35865]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271390","summary":null,"start":101339917,"end":101340934,"strand":1,"description":"ribosomal protein L21 pseudogene 132 [Source:HGNC Symbol;Acc:HGNC:35865]"}, {"versioned_ensembl_gene_id":"ENSG00000230755.1","gene_symbol":"MTATP6P23","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075300","summary":null,"start":69589880,"end":69590355,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:52179]"}, {"versioned_ensembl_gene_id":"ENSG00000238132.2","gene_symbol":"CASC4P1","gene_name":"cancer susceptibility 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39251]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420689","summary":null,"start":19563589,"end":19564900,"strand":-1,"description":"cancer susceptibility 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39251]"}, {"versioned_ensembl_gene_id":"ENSG00000215572.2","gene_symbol":"ESRRAP1","gene_name":"estrogen-related receptor alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3472]","synonyms":"ESRRAP","biotype":"processed_pseudogene","ncbi_id":"144847","summary":null,"start":19560013,"end":19561269,"strand":-1,"description":"estrogen-related receptor alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3472]"}, {"versioned_ensembl_gene_id":"ENSG00000168925.10","gene_symbol":"CTRB1","gene_name":"chymotrypsinogen B1 [Source:HGNC Symbol;Acc:HGNC:2521]","synonyms":"CTRB","biotype":"protein_coding","ncbi_id":"1504","summary":"This gene encodes a member of the serine protease family of enzymes and forms a principal precursor of the pancreatic proteolytic enzymes. The encoded preproprotein is synthesized in the acinar cells of the pancreas and secreted into the small intestine where it undergoes proteolytic activation to generate a functional enzyme. This CTRB1 gene is located head-to-head with the related CTRB2 gene. Some human populations have an alternate haplotype which inverts a 16.6 Kb region containing portions of intron 1, exon 1, and the upstream sequence of the CTRB1 and CTRB2 genes. In this inversion haplotype exon 1 and flanking sequence is swapped in CTRB1 and CTRB2. This inversion is associated with differential gene expression and increased risk for chronic pancreatitis. The GRCh38 assembly represents the minor allele for SNP rs8048956 of the CTRB1 gene. SNP rs8048956 in intron 1 of the CTRB2 gene is diagnostic for this inversion. This CTRB1 gene encodes distinct isoforms, some or all of which may undergo similar processing to generate the mature protein. [provided by RefSeq, Jan 2021]","start":75219000,"end":75224924,"strand":1,"description":"chymotrypsinogen B1 [Source:HGNC Symbol;Acc:HGNC:2521]"}, {"versioned_ensembl_gene_id":"ENSG00000140749.8","gene_symbol":"IGSF6","gene_name":"immunoglobulin superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:5953]","synonyms":"DORA","biotype":"protein_coding","ncbi_id":"10261","summary":null,"start":21639537,"end":21652660,"strand":-1,"description":"immunoglobulin superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:5953]"}, {"versioned_ensembl_gene_id":"ENSG00000266524.2","gene_symbol":"GDF10","gene_name":"growth differentiation factor 10 [Source:HGNC Symbol;Acc:HGNC:4215]","synonyms":"BMP-3b","biotype":"protein_coding","ncbi_id":"2662","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This promotes neural repair after stroke. Additionally, this protein may act as a tumor suppressor and reduced expression of this gene is associated with oral cancer. [provided by RefSeq, Jul 2016]","start":47300386,"end":47313547,"strand":1,"description":"growth differentiation factor 10 [Source:HGNC Symbol;Acc:HGNC:4215]"}, {"versioned_ensembl_gene_id":"ENSG00000258440.1","gene_symbol":"AL118557.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52155740,"end":52156179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254801.1","gene_symbol":"AC084851.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49070752,"end":49071000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249021.1","gene_symbol":"AC008549.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115691462,"end":115692167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248709.1","gene_symbol":"AC008549.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115755644,"end":115756286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170571.11","gene_symbol":"EMB","gene_name":"embigin [Source:HGNC Symbol;Acc:HGNC:30465]","synonyms":"MGC71745","biotype":"protein_coding","ncbi_id":"133418","summary":"This gene encodes a transmembrane glycoprotein that is a member of the immunoglobulin superfamily. The encoded protein may be involved in cell growth and development by mediating interactions between the cell and extracellular matrix. A pseudogene of this gene is found on chromosome 1. [provided by RefSeq, Jan 2009]","start":50396192,"end":50443248,"strand":-1,"description":"embigin [Source:HGNC Symbol;Acc:HGNC:30465]"}, {"versioned_ensembl_gene_id":"ENSG00000183258.11","gene_symbol":"DDX41","gene_name":"DEAD-box helicase 41 [Source:HGNC Symbol;Acc:HGNC:18674]","synonyms":"MGC8828,ABS","biotype":"protein_coding","ncbi_id":"51428","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a member of the DEAD box protein family and interacts with several spliceosomal proteins. In addition, the encoded protein may recognize the bacterial second messengers cyclic di-GMP and cyclic di-AMP, resulting in the induction of genes involved in the innate immune response. [provided by RefSeq, Jan 2017]","start":177511577,"end":177517469,"strand":-1,"description":"DEAD-box helicase 41 [Source:HGNC Symbol;Acc:HGNC:18674]"}, {"versioned_ensembl_gene_id":"ENSG00000229826.2","gene_symbol":"AC244505.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52735901,"end":52736107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250430.1","gene_symbol":"AC106872.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165026261,"end":165026944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276892.1","gene_symbol":"AL022401.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85851575,"end":85851682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284373.1","gene_symbol":"AC106774.8","gene_name":"Putative TAF11-like protein ENSP00000332601 [Source:UniProtKB/Swiss-Prot;Acc:A6NLC8]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17498231,"end":17498827,"strand":1,"description":"Putative TAF11-like protein ENSP00000332601 [Source:UniProtKB/Swiss-Prot;Acc:A6NLC8]"}, {"versioned_ensembl_gene_id":"ENSG00000101247.17","gene_symbol":"NDUFAF5","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:15899]","synonyms":"dJ842G6.1,C20orf7","biotype":"protein_coding","ncbi_id":"79133","summary":"The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":13784950,"end":13821582,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:15899]"}, {"versioned_ensembl_gene_id":"ENSG00000215297.3","gene_symbol":"AL354941.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3364329,"end":3364792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276870.2","gene_symbol":"PLA2G10","gene_name":"phospholipase A2 group X [Source:HGNC Symbol;Acc:HGNC:9029]","synonyms":"GXPLA2","biotype":"protein_coding","ncbi_id":"8399","summary":"This gene encodes a member of the phospholipase A2 family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This calcium-dependent enzyme hydrolyzes glycerophospholipids to produce free fatty acids and lysophospholipids. In one example, this enzyme catalyzes the release of arachidonic acid from cell membrane phospholipids, thus playing a role in the production of various inflammatory lipid mediators, such as prostaglandins. The encoded protein may promote the survival of breast cancer cells through its role in lipid metabolism. [provided by RefSeq, Nov 2015]","start":14672547,"end":14694674,"strand":-1,"description":"phospholipase A2 group X [Source:HGNC Symbol;Acc:HGNC:9029]"}, {"versioned_ensembl_gene_id":"ENSG00000168246.5","gene_symbol":"UBTD2","gene_name":"ubiquitin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24463]","synonyms":"MGC30022,DC-UbP","biotype":"protein_coding","ncbi_id":"92181","summary":null,"start":172209640,"end":172284071,"strand":-1,"description":"ubiquitin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24463]"}, {"versioned_ensembl_gene_id":"ENSG00000164308.16","gene_symbol":"ERAP2","gene_name":"endoplasmic reticulum aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:29499]","synonyms":"LRAP,L-RAP","biotype":"protein_coding","ncbi_id":"64167","summary":"This gene encodes a zinc metalloaminopeptidase of the M1 protease family that resides in the endoplasmic reticulum and functions in N-terminal trimming antigenic epitopes for presentation by major histocompatibility complex (MHC) class I molecules. Certain mutations in this gene are associated with the inflammatory arthritis syndrome ankylosing spondylitis and pre-eclampsia. This gene is located adjacent to a closely related aminopeptidase gene on chromosome 5. [provided by RefSeq, Jul 2016]","start":96875939,"end":96919716,"strand":1,"description":"endoplasmic reticulum aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:29499]"}, {"versioned_ensembl_gene_id":"ENSG00000176868.2","gene_symbol":"AL358781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131497479,"end":131500191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282532.1","gene_symbol":"AC016482.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37142069,"end":37142882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272574.1","gene_symbol":"AL596325.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":162593103,"end":162593754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234961.1","gene_symbol":"AL133415.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17233325,"end":17234833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270135.1","gene_symbol":"AC078795.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169793495,"end":169793966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237636.2","gene_symbol":"ANKRD26P3","gene_name":"ankyrin repeat domain 26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39689]","synonyms":"LINC00414","biotype":"unprocessed_pseudogene","ncbi_id":"100101938","summary":null,"start":19290593,"end":19344825,"strand":-1,"description":"ankyrin repeat domain 26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39689]"}, {"versioned_ensembl_gene_id":"ENSG00000198517.9","gene_symbol":"MAFK","gene_name":"MAF bZIP transcription factor K [Source:HGNC Symbol;Acc:HGNC:6782]","synonyms":"P18,NFE2U","biotype":"protein_coding","ncbi_id":"7975","summary":"The developmentally regulated expression of the globin genes depends on upstream regulatory elements termed locus control regions (LCRs). LCRs are associated with powerful enhancer activity that is mediated by the transcription factor NFE2 (nuclear factor erythroid-2). NFE2 recognition sites are also present in the gene promoters of 2 heme biosynthetic enzymes, porphobilinogen deaminase (PBGD; MIM 609806) and ferrochelatase (FECH; MIM 612386). NFE2 DNA-binding activity consists of a heterodimer containing an 18-kD Maf protein (MafF, MafG (MIM 602020), or MafK) and p45 (MIM 601490). Both subunits are members of the activator protein-1 superfamily of basic leucine zipper (bZIP) proteins (see MIM 165160). Maf homodimers suppress transcription at NFE2 sites.[supplied by OMIM, Nov 2008]","start":1530714,"end":1543043,"strand":1,"description":"MAF bZIP transcription factor K [Source:HGNC Symbol;Acc:HGNC:6782]"}, {"versioned_ensembl_gene_id":"ENSG00000180708.5","gene_symbol":"OR10K2","gene_name":"olfactory receptor family 10 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14826]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391107","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158418210,"end":158426237,"strand":-1,"description":"olfactory receptor family 10 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14826]"}, {"versioned_ensembl_gene_id":"ENSG00000167524.14","gene_symbol":"SGK494","gene_name":"uncharacterized serine/threonine-protein kinase SgK494 [Source:NCBI gene;Acc:124923]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124923","summary":null,"start":28607964,"end":28614200,"strand":-1,"description":"uncharacterized serine/threonine-protein kinase SgK494 [Source:NCBI gene;Acc:124923]"}, {"versioned_ensembl_gene_id":"ENSG00000186306.1","gene_symbol":"OR10T2","gene_name":"olfactory receptor family 10 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128360","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158398522,"end":158399466,"strand":-1,"description":"olfactory receptor family 10 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14816]"}, {"versioned_ensembl_gene_id":"ENSG00000226914.1","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32807865,"end":32808542,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000166603.4","gene_symbol":"MC4R","gene_name":"melanocortin 4 receptor [Source:HGNC Symbol;Acc:HGNC:6932]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4160","summary":"The protein encoded by this gene is a membrane-bound receptor and member of the melanocortin receptor family. The encoded protein interacts with adrenocorticotropic and MSH hormones and is mediated by G proteins. This is an intronless gene. Defects in this gene are a cause of autosomal dominant obesity. [provided by RefSeq, Jan 2010]","start":60371110,"end":60372775,"strand":-1,"description":"melanocortin 4 receptor [Source:HGNC Symbol;Acc:HGNC:6932]"}, {"versioned_ensembl_gene_id":"ENSG00000275491.1","gene_symbol":"LINC01730","gene_name":"long intergenic non-protein coding RNA 1730 [Source:HGNC Symbol;Acc:HGNC:52518]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929125","summary":null,"start":3808357,"end":3812434,"strand":1,"description":"long intergenic non-protein coding RNA 1730 [Source:HGNC Symbol;Acc:HGNC:52518]"}, {"versioned_ensembl_gene_id":"ENSG00000254674.1","gene_symbol":"OR4A42P","gene_name":"olfactory receptor family 4 subfamily A member 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:31261]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403248","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48610063,"end":48611000,"strand":1,"description":"olfactory receptor family 4 subfamily A member 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:31261]"}, {"versioned_ensembl_gene_id":"ENSG00000206296.8","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32772781,"end":32775190,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000124429.17","gene_symbol":"POF1B","gene_name":"premature ovarian failure, 1B [Source:HGNC Symbol;Acc:HGNC:13711]","synonyms":"POF,FLJ22792","biotype":"protein_coding","ncbi_id":"79983","summary":"Premature ovarian failure (POF) is characterized by primary or secondary amenorrhea in women less than 40 years old. Two POF susceptibility regions called \"POF1\" and \"POF2\" have been identified by breakpoint mapping of X-autosome translocations. POF1 extends from Xq21-qter while POF2 extends from Xq13.3 to Xq21.1. This gene, POF1B, resides in the POF2 region. This gene is expressed at trace levels in mouse prenatal ovary and is barely detectable or absent from adult ovary, in human and in the mouse respectively. This gene's expression is restricted to epithelia with its highest expression in the epidermis, and oro-pharyngeal and gastro-intestinal tracts. The protein encoded by this gene binds non-muscle actin filaments. The role this gene may play in the etiology of premature ovarian failure remains to be determined. [provided by RefSeq, Jan 2010]","start":85277396,"end":85379743,"strand":-1,"description":"premature ovarian failure, 1B [Source:HGNC Symbol;Acc:HGNC:13711]"}, {"versioned_ensembl_gene_id":"ENSG00000160539.4","gene_symbol":"PLPP7","gene_name":"phospholipid phosphatase 7 (inactive) [Source:HGNC Symbol;Acc:HGNC:28174]","synonyms":"PPAPDC3,NET39,MGC12921,FLJ14662,C9orf67","biotype":"protein_coding","ncbi_id":"84814","summary":null,"start":131289694,"end":131309262,"strand":1,"description":"phospholipid phosphatase 7 (inactive) [Source:HGNC Symbol;Acc:HGNC:28174]"}, {"versioned_ensembl_gene_id":"ENSG00000259754.1","gene_symbol":"AC092078.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47884310,"end":48049112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095383.19","gene_symbol":"TBC1D2","gene_name":"TBC1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:18026]","synonyms":"TBC1D2A,PARIS1,Armus","biotype":"protein_coding","ncbi_id":"55357","summary":null,"start":98198999,"end":98255721,"strand":-1,"description":"TBC1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:18026]"}, {"versioned_ensembl_gene_id":"ENSG00000259730.1","gene_symbol":"AC092078.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47944044,"end":47949509,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260823.1","gene_symbol":"AC026461.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56609501,"end":56611375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248645.1","gene_symbol":"AC106872.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":164938322,"end":164939990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169385.2","gene_symbol":"RNASE2","gene_name":"ribonuclease A family member 2 [Source:HGNC Symbol;Acc:HGNC:10045]","synonyms":"RNS2,RAF3,EDN","biotype":"protein_coding","ncbi_id":"6036","summary":"The protein encoded by this gene is a non-secretory ribonuclease that belongs to the pancreatic ribonuclease family, a subset of the ribonuclease A superfamily. The protein antimicrobial activity against viruses. [provided by RefSeq, Oct 2014]","start":20955452,"end":20956436,"strand":1,"description":"ribonuclease A family member 2 [Source:HGNC Symbol;Acc:HGNC:10045]"}, {"versioned_ensembl_gene_id":"ENSG00000255163.1","gene_symbol":"HSPE1P18","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49337]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480257","summary":null,"start":118208932,"end":118209211,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49337]"}, {"versioned_ensembl_gene_id":"ENSG00000232243.1","gene_symbol":"AL139327.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19262797,"end":19263873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213607.4","gene_symbol":"OR4A45P","gene_name":"olfactory receptor family 4 subfamily A member 45 pseudogene [Source:HGNC Symbol;Acc:HGNC:31264]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403251","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48579436,"end":48580336,"strand":1,"description":"olfactory receptor family 4 subfamily A member 45 pseudogene [Source:HGNC Symbol;Acc:HGNC:31264]"}, {"versioned_ensembl_gene_id":"ENSG00000164366.3","gene_symbol":"CCDC127","gene_name":"coiled-coil domain containing 127 [Source:HGNC Symbol;Acc:HGNC:30520]","synonyms":"FLJ25701","biotype":"protein_coding","ncbi_id":"133957","summary":null,"start":196871,"end":218215,"strand":-1,"description":"coiled-coil domain containing 127 [Source:HGNC Symbol;Acc:HGNC:30520]"}, {"versioned_ensembl_gene_id":"ENSG00000236227.8","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"RING3,BRD2-IT1,FSRG1,NAT,D6S113E,KIAA9001","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":33002124,"end":33012662,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000255304.1","gene_symbol":"OR4A46P","gene_name":"olfactory receptor family 4 subfamily A member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:31265]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403252","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48496348,"end":48497280,"strand":1,"description":"olfactory receptor family 4 subfamily A member 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:31265]"}, {"versioned_ensembl_gene_id":"ENSG00000234792.1","gene_symbol":"AL450023.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52612656,"end":52613523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179057.13","gene_symbol":"IGSF22","gene_name":"immunoglobulin superfamily member 22 [Source:HGNC Symbol;Acc:HGNC:26750]","synonyms":"IGFN2,FLJ37794","biotype":"protein_coding","ncbi_id":"283284","summary":null,"start":18704305,"end":18726230,"strand":-1,"description":"immunoglobulin superfamily member 22 [Source:HGNC Symbol;Acc:HGNC:26750]"}, {"versioned_ensembl_gene_id":"ENSG00000226799.1","gene_symbol":"CR936918.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29266972,"end":29267126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232710.1","gene_symbol":"AC254562.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42136433,"end":42139927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268799.2","gene_symbol":"AC106774.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17491361,"end":17491769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007202.14","gene_symbol":"KIAA0100","gene_name":"KIAA0100 [Source:HGNC Symbol;Acc:HGNC:28960]","synonyms":"MGC111488,FMP27,DKFZp686M0843,CT101,BCOX1,BCOX","biotype":"protein_coding","ncbi_id":"9703","summary":"This gene was initially characterized in human as having high expression levels in breast carcinomas and breast cancer cell lines. This gene also has increased expression in prostrate cancer cells relative to normal prostrate tissues. Expression of this gene is negatively regulated by direct binding of the microRNA miR-195 to its 3' UTR. miR-195 has been shown to modulate the invasiveness of prostrate cancer cells and xenograft metastases by downgrading expression of this gene. In mouse, the protein encoded by this gene was identified as an antigen on acute monocytic leukemia cells. In human, alternative splicing results in multiple transcript variants encoding distinct isoforms; some of these isoforms are predicted to contain an RNA pol II promoter FMP27 protein domain and a Golgi-body-localization APT1 domain. [provided by RefSeq, Apr 2017]","start":28614440,"end":28645454,"strand":-1,"description":"KIAA0100 [Source:HGNC Symbol;Acc:HGNC:28960]"}, {"versioned_ensembl_gene_id":"ENSG00000174527.9","gene_symbol":"MYO1H","gene_name":"myosin IH [Source:HGNC Symbol;Acc:HGNC:13879]","synonyms":"FLJ37587","biotype":"protein_coding","ncbi_id":"283446","summary":null,"start":109347903,"end":109455523,"strand":1,"description":"myosin IH [Source:HGNC Symbol;Acc:HGNC:13879]"}, {"versioned_ensembl_gene_id":"ENSG00000234999.1","gene_symbol":"SNRPCP19","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49834]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310849","summary":null,"start":24906135,"end":24906594,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49834]"}, {"versioned_ensembl_gene_id":"ENSG00000260862.1","gene_symbol":"AC099506.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":82773319,"end":82829638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235620.1","gene_symbol":"AC020743.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50274790,"end":50275622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228767.1","gene_symbol":"KRT8P18","gene_name":"keratin 8 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:33370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442078","summary":null,"start":35215705,"end":35217149,"strand":-1,"description":"keratin 8 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:33370]"}, {"versioned_ensembl_gene_id":"ENSG00000178084.1","gene_symbol":"HTR3C","gene_name":"5-hydroxytryptamine receptor 3C [Source:HGNC Symbol;Acc:HGNC:24003]","synonyms":null,"biotype":"protein_coding","ncbi_id":"170572","summary":"The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit C of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor causes fast, depolarizing responses in neurons after activation. Genes encoding subunits C, D and E form a cluster on chromosome 3. [provided by RefSeq, Jul 2008]","start":184053047,"end":184060671,"strand":1,"description":"5-hydroxytryptamine receptor 3C [Source:HGNC Symbol;Acc:HGNC:24003]"}, {"versioned_ensembl_gene_id":"ENSG00000277289.1","gene_symbol":"BX510359.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52531709,"end":52532051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226523.1","gene_symbol":"AC074375.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42680088,"end":42680279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260788.5","gene_symbol":"AC009063.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83721119,"end":83772936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138107.12","gene_symbol":"ACTR1A","gene_name":"ARP1 actin related protein 1 homolog A [Source:HGNC Symbol;Acc:HGNC:167]","synonyms":"Arp1A,ARP1","biotype":"protein_coding","ncbi_id":"10121","summary":"This gene encodes a 42.6 kD subunit of dynactin, a macromolecular complex consisting of 10-11 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit is present in 8-13 copies per dynactin molecule, and is the most abundant molecule in the dynactin complex. It is an actin-related protein, and is approximately 60% identical at the amino acid level to conventional actin. [provided by RefSeq, Jul 2008]","start":102461881,"end":102502711,"strand":-1,"description":"ARP1 actin related protein 1 homolog A [Source:HGNC Symbol;Acc:HGNC:167]"}, {"versioned_ensembl_gene_id":"ENSG00000218754.4","gene_symbol":"RPL18AP8","gene_name":"ribosomal protein L18a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36984]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644082","summary":null,"start":96619304,"end":96619831,"strand":1,"description":"ribosomal protein L18a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36984]"}, {"versioned_ensembl_gene_id":"ENSG00000211452.10","gene_symbol":"DIO1","gene_name":"iodothyronine deiodinase 1 [Source:HGNC Symbol;Acc:HGNC:2883]","synonyms":"TXDI1","biotype":"protein_coding","ncbi_id":"1733","summary":"The protein encoded by this gene belongs to the iodothyronine deiodinase family. It catalyzes the activation, as well as the inactivation of thyroid hormone by outer and inner ring deiodination, respectively. The activation reaction involves the conversion of the prohormone thyroxine (3,5,3',5'-tetraiodothyronine, T4), secreted by the thyroid gland, to the bioactive thyroid hormone (3,5,3'-triiodothyronine, T3) by 5'-deiodination. This protein provides most of the circulating T3, which is essential for growth, differentiation and basal metabolism in vertebrates. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2018]","start":53891239,"end":53911086,"strand":1,"description":"iodothyronine deiodinase 1 [Source:HGNC Symbol;Acc:HGNC:2883]"}, {"versioned_ensembl_gene_id":"ENSG00000110786.17","gene_symbol":"PTPN5","gene_name":"protein tyrosine phosphatase, non-receptor type 5 [Source:HGNC Symbol;Acc:HGNC:9657]","synonyms":"STEP61,STEP,PTPSTEP","biotype":"protein_coding","ncbi_id":"84867","summary":null,"start":18727928,"end":18792721,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 5 [Source:HGNC Symbol;Acc:HGNC:9657]"}, {"versioned_ensembl_gene_id":"ENSG00000264538.6","gene_symbol":"SUZ12P1","gene_name":"SUZ12 polycomb repressive complex 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32421]","synonyms":"SUZ12P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440423","summary":null,"start":30709299,"end":30790908,"strand":1,"description":"SUZ12 polycomb repressive complex 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32421]"}, {"versioned_ensembl_gene_id":"ENSG00000213213.13","gene_symbol":"CCDC183","gene_name":"coiled-coil domain containing 183 [Source:HGNC Symbol;Acc:HGNC:28236]","synonyms":"MGC15438,KIAA1984,bA216L13.7","biotype":"protein_coding","ncbi_id":"84960","summary":null,"start":136796350,"end":136807741,"strand":1,"description":"coiled-coil domain containing 183 [Source:HGNC Symbol;Acc:HGNC:28236]"}, {"versioned_ensembl_gene_id":"ENSG00000151117.8","gene_symbol":"TMEM86A","gene_name":"transmembrane protein 86A [Source:HGNC Symbol;Acc:HGNC:26890]","synonyms":"FLJ90119","biotype":"protein_coding","ncbi_id":"144110","summary":null,"start":18693122,"end":18704785,"strand":1,"description":"transmembrane protein 86A [Source:HGNC Symbol;Acc:HGNC:26890]"}, {"versioned_ensembl_gene_id":"ENSG00000223395.2","gene_symbol":"RBM22P7","gene_name":"RNA binding motif protein 22 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39700]","synonyms":"RBM22P9","biotype":"processed_pseudogene","ncbi_id":"106478953","summary":null,"start":52509903,"end":52510182,"strand":1,"description":"RNA binding motif protein 22 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39700]"}, {"versioned_ensembl_gene_id":"ENSG00000242259.8","gene_symbol":"C22orf39","gene_name":"chromosome 22 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:27012]","synonyms":"MGC74441","biotype":"protein_coding","ncbi_id":"128977","summary":null,"start":19351368,"end":19448232,"strand":-1,"description":"chromosome 22 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:27012]"}, {"versioned_ensembl_gene_id":"ENSG00000273300.1","gene_symbol":"AC000068.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19454179,"end":19454605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185065.6","gene_symbol":"AC000068.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19447893,"end":19450105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224556.2","gene_symbol":"BX510359.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52422069,"end":52459066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228954.1","gene_symbol":"BX927178.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31351206,"end":31351939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280412.1","gene_symbol":"AC004790.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16019719,"end":16020290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229147.1","gene_symbol":"SMPD4P2","gene_name":"sphingomyelin phosphodiesterase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39674]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441654","summary":null,"start":19152567,"end":19171194,"strand":-1,"description":"sphingomyelin phosphodiesterase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39674]"}, {"versioned_ensembl_gene_id":"ENSG00000131188.11","gene_symbol":"PRR7","gene_name":"proline rich 7, synaptic [Source:HGNC Symbol;Acc:HGNC:28130]","synonyms":"MGC10772","biotype":"protein_coding","ncbi_id":"80758","summary":null,"start":177446445,"end":177456286,"strand":1,"description":"proline rich 7, synaptic [Source:HGNC Symbol;Acc:HGNC:28130]"}, {"versioned_ensembl_gene_id":"ENSG00000177614.10","gene_symbol":"PGBD5","gene_name":"piggyBac transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:19405]","synonyms":"FLJ11413,DKFZp761A0620","biotype":"protein_coding","ncbi_id":"79605","summary":"The piggyBac family of proteins, found in diverse animals, are transposases related to the transposase of the canonical piggyBac transposon from the moth, Trichoplusia ni. This family also includes genes in several genomes, including human, that appear to have been derived from the piggyBac transposons. This gene belongs to the subfamily of piggyBac transposable element derived (PGBD) genes. The PGBD proteins appear to be novel, with no obvious relationship to other transposases, or other known protein families. [provided by RefSeq, May 2010]","start":230314482,"end":230426371,"strand":-1,"description":"piggyBac transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:19405]"}, {"versioned_ensembl_gene_id":"ENSG00000135443.8","gene_symbol":"KRT85","gene_name":"keratin 85 [Source:HGNC Symbol;Acc:HGNC:6462]","synonyms":"KRTHB5,Hb-5","biotype":"protein_coding","ncbi_id":"3891","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. [provided by RefSeq, Jul 2008]","start":52360006,"end":52367481,"strand":-1,"description":"keratin 85 [Source:HGNC Symbol;Acc:HGNC:6462]"}, {"versioned_ensembl_gene_id":"ENSG00000249944.1","gene_symbol":"AC008628.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115489634,"end":115489931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249766.1","gene_symbol":"AC097535.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33400538,"end":33400679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248734.2","gene_symbol":"AC008906.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96784777,"end":96785999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233974.3","gene_symbol":"AC138951.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21481327,"end":21484011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250551.1","gene_symbol":"MIR583HG","gene_name":"MIR583 host gene [Source:HGNC Symbol;Acc:HGNC:53061]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984114","summary":null,"start":96050115,"end":96215519,"strand":1,"description":"MIR583 host gene [Source:HGNC Symbol;Acc:HGNC:53061]"}, {"versioned_ensembl_gene_id":"ENSG00000243234.1","gene_symbol":"AC010326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57953158,"end":57953759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230029.1","gene_symbol":"CDY11P","gene_name":"chromodomain protein Y-linked 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:23852]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378014","summary":null,"start":21696570,"end":21698220,"strand":1,"description":"chromodomain protein Y-linked 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:23852]"}, {"versioned_ensembl_gene_id":"ENSG00000250955.1","gene_symbol":"AC008592.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95964999,"end":95986311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237023.1","gene_symbol":"USP9YP3","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37739]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387364","summary":null,"start":21661926,"end":21674008,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37739]"}, {"versioned_ensembl_gene_id":"ENSG00000223893.1","gene_symbol":"GNL2P1","gene_name":"G protein nucleolar 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270790","summary":null,"start":49942251,"end":49944440,"strand":-1,"description":"G protein nucleolar 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50779]"}, {"versioned_ensembl_gene_id":"ENSG00000132541.10","gene_symbol":"RIDA","gene_name":"reactive intermediate imine deaminase A homolog [Source:HGNC Symbol;Acc:HGNC:16897]","synonyms":"UK114,PSP,P14.5,HRSP12","biotype":"protein_coding","ncbi_id":"10247","summary":null,"start":98102344,"end":98117241,"strand":-1,"description":"reactive intermediate imine deaminase A homolog [Source:HGNC Symbol;Acc:HGNC:16897]"}, {"versioned_ensembl_gene_id":"ENSG00000120457.11","gene_symbol":"KCNJ5","gene_name":"potassium voltage-gated channel subfamily J member 5 [Source:HGNC Symbol;Acc:HGNC:6266]","synonyms":"LQT13,Kir3.4,KATP1,GIRK4,CIR","biotype":"protein_coding","ncbi_id":"3762","summary":"This gene encodes an integral membrane protein which belongs to one of seven subfamilies of inward-rectifier potassium channel proteins called potassium channel subfamily J. The encoded protein is a subunit of the potassium channel which is homotetrameric. It is controlled by G-proteins and has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Naturally occurring mutations in this gene are associated with aldosterone-producing adenomas. [provided by RefSeq, Aug 2017]","start":128891356,"end":128921035,"strand":1,"description":"potassium voltage-gated channel subfamily J member 5 [Source:HGNC Symbol;Acc:HGNC:6266]"}, {"versioned_ensembl_gene_id":"ENSG00000274240.2","gene_symbol":"AC136352.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21293635,"end":21295183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156689.6","gene_symbol":"GLYATL2","gene_name":"glycine-N-acyltransferase like 2 [Source:HGNC Symbol;Acc:HGNC:24178]","synonyms":"MGC24009,BXMAS2-10","biotype":"protein_coding","ncbi_id":"219970","summary":null,"start":58834065,"end":58904215,"strand":-1,"description":"glycine-N-acyltransferase like 2 [Source:HGNC Symbol;Acc:HGNC:24178]"}, {"versioned_ensembl_gene_id":"ENSG00000257696.1","gene_symbol":"AC010203.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100143058,"end":100144671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284701.1","gene_symbol":"TMEM247","gene_name":"transmembrane protein 247 [Source:HGNC Symbol;Acc:HGNC:42967]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388946","summary":null,"start":46479565,"end":46484425,"strand":1,"description":"transmembrane protein 247 [Source:HGNC Symbol;Acc:HGNC:42967]"}, {"versioned_ensembl_gene_id":"ENSG00000271618.1","gene_symbol":"AL359821.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71738173,"end":71738354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261469.1","gene_symbol":"AC020978.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68236845,"end":68237667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242068.1","gene_symbol":"AC108734.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180772750,"end":180773914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250782.1","gene_symbol":"AC233724.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17634460,"end":17635053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240210.3","gene_symbol":"AL122013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68338728,"end":68339528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266803.1","gene_symbol":"AC127540.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16557985,"end":16559269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214814.7","gene_symbol":"FER1L6","gene_name":"fer-1 like family member 6 [Source:HGNC Symbol;Acc:HGNC:28065]","synonyms":"C8ORFK23","biotype":"protein_coding","ncbi_id":"654463","summary":null,"start":123851987,"end":124120061,"strand":1,"description":"fer-1 like family member 6 [Source:HGNC Symbol;Acc:HGNC:28065]"}, {"versioned_ensembl_gene_id":"ENSG00000126890.13","gene_symbol":"CTAG2","gene_name":"cancer/testis antigen 2 [Source:HGNC Symbol;Acc:HGNC:2492]","synonyms":"MGC3803,MGC138724,LAGE1,LAGE-1b,LAGE-1a,LAGE-1,ESO2,CT6.2b,CT6.2a,CAMEL","biotype":"protein_coding","ncbi_id":"30848","summary":"This gene encodes an autoimmunogenic tumor antigen that belongs to the ESO/LAGE family of cancer-testis antigens. This protein is expressed in a wide array of cancers including melanoma, breast cancer, bladder cancer and prostate cancer. This protein is also expressed in normal testis tissue. An alternative open reading frame product of this gene has been described in PMID:10399963. This alternate protein, termed CAMEL, is a tumor antigen that is recognized by melanoma-specific cytotoxic T-lymphocytes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":154651972,"end":154653579,"strand":-1,"description":"cancer/testis antigen 2 [Source:HGNC Symbol;Acc:HGNC:2492]"}, {"versioned_ensembl_gene_id":"ENSG00000074201.8","gene_symbol":"CLNS1A","gene_name":"chloride nucleotide-sensitive channel 1A [Source:HGNC Symbol;Acc:HGNC:2080]","synonyms":"ICln,CLCI","biotype":"protein_coding","ncbi_id":"1207","summary":"This gene encodes a protein that functions in multiple regulatory pathways. The encoded protein complexes with numerous cytosolic proteins and performs diverse functions including regulation of small nuclear ribonucleoprotein biosynthesis, platelet activation and cytoskeletal organization. The protein is also found associated with the plasma membrane where it functions as a chloride current regulator. Pseudogenes of this gene are found on chromosomes 1, 4 and 6. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":77514936,"end":77637805,"strand":-1,"description":"chloride nucleotide-sensitive channel 1A [Source:HGNC Symbol;Acc:HGNC:2080]"}, {"versioned_ensembl_gene_id":"ENSG00000234361.1","gene_symbol":"AL391863.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157829143,"end":157830573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253885.1","gene_symbol":"ARF1P3","gene_name":"ADP ribosylation factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39884]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442396","summary":null,"start":124151923,"end":124152433,"strand":1,"description":"ADP ribosylation factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39884]"}, {"versioned_ensembl_gene_id":"ENSG00000242393.1","gene_symbol":"AC010141.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21508299,"end":21510470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274863.1","gene_symbol":"AL135936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19000709,"end":19056796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079308.16","gene_symbol":"TNS1","gene_name":"tensin 1 [Source:HGNC Symbol;Acc:HGNC:11973]","synonyms":"DKFZp586K0617,TNS,PPP1R155,MXRA6","biotype":"protein_coding","ncbi_id":"7145","summary":"The protein encoded by this gene localizes to focal adhesions, regions of the plasma membrane where the cell attaches to the extracellular matrix. This protein crosslinks actin filaments and contains a Src homology 2 (SH2) domain, which is often found in molecules involved in signal transduction. This protein is a substrate of calpain II. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":217799789,"end":218002995,"strand":-1,"description":"tensin 1 [Source:HGNC Symbol;Acc:HGNC:11973]"}, {"versioned_ensembl_gene_id":"ENSG00000235173.6","gene_symbol":"HGH1","gene_name":"HGH1 homolog [Source:HGNC Symbol;Acc:HGNC:24161]","synonyms":"LOC51236,FLJ40907,FAM203B,FAM203A,C8orf30B,C8orf30A,Brp16","biotype":"protein_coding","ncbi_id":"51236","summary":null,"start":144137769,"end":144140843,"strand":1,"description":"HGH1 homolog [Source:HGNC Symbol;Acc:HGNC:24161]"}, {"versioned_ensembl_gene_id":"ENSG00000270021.1","gene_symbol":"AC026691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135399280,"end":135401296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218868.1","gene_symbol":"CNN3P1","gene_name":"calponin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38666]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643875","summary":null,"start":6534697,"end":6535631,"strand":1,"description":"calponin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38666]"}, {"versioned_ensembl_gene_id":"ENSG00000158169.12","gene_symbol":"FANCC","gene_name":"Fanconi anemia complementation group C [Source:HGNC Symbol;Acc:HGNC:3584]","synonyms":"FAC,FA3,FACC","biotype":"protein_coding","ncbi_id":"2176","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group C. [provided by RefSeq, Jul 2008]","start":95099054,"end":95426796,"strand":-1,"description":"Fanconi anemia complementation group C [Source:HGNC Symbol;Acc:HGNC:3584]"}, {"versioned_ensembl_gene_id":"ENSG00000282805.1","gene_symbol":"AC023315.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37000430,"end":37001866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233484.2","gene_symbol":"AL450471.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":84403898,"end":84404024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259746.1","gene_symbol":"HSPE1P3","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49322]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507046","summary":null,"start":90634725,"end":90635033,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49322]"}, {"versioned_ensembl_gene_id":"ENSG00000233430.3","gene_symbol":"AC239798.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143811359,"end":143825837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167491.17","gene_symbol":"GATAD2A","gene_name":"GATA zinc finger domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29989]","synonyms":"p66alpha","biotype":"protein_coding","ncbi_id":"54815","summary":null,"start":19385826,"end":19508931,"strand":1,"description":"GATA zinc finger domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29989]"}, {"versioned_ensembl_gene_id":"ENSG00000176261.15","gene_symbol":"ZBTB8OS","gene_name":"zinc finger and BTB domain containing 8 opposite strand [Source:HGNC Symbol;Acc:HGNC:24094]","synonyms":"ARCH","biotype":"protein_coding","ncbi_id":"339487","summary":null,"start":32600172,"end":32650903,"strand":-1,"description":"zinc finger and BTB domain containing 8 opposite strand [Source:HGNC Symbol;Acc:HGNC:24094]"}, {"versioned_ensembl_gene_id":"ENSG00000231993.1","gene_symbol":"EP300-AS1","gene_name":"EP300 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50504]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927279","summary":null,"start":41174591,"end":41197456,"strand":-1,"description":"EP300 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50504]"}, {"versioned_ensembl_gene_id":"ENSG00000105136.20","gene_symbol":"ZNF419","gene_name":"zinc finger protein 419 [Source:HGNC Symbol;Acc:HGNC:20648]","synonyms":"ZNF419A,ZAPHIR","biotype":"protein_coding","ncbi_id":"79744","summary":null,"start":57487711,"end":57496097,"strand":1,"description":"zinc finger protein 419 [Source:HGNC Symbol;Acc:HGNC:20648]"}, {"versioned_ensembl_gene_id":"ENSG00000253510.1","gene_symbol":"AC004944.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5506068,"end":5509126,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204311.12","gene_symbol":"DFNB59","gene_name":"deafness, autosomal recessive 59 [Source:HGNC Symbol;Acc:HGNC:29502]","synonyms":"pejvakin","biotype":"protein_coding","ncbi_id":"494513","summary":"The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008]","start":178451436,"end":178461390,"strand":1,"description":"deafness, autosomal recessive 59 [Source:HGNC Symbol;Acc:HGNC:29502]"}, {"versioned_ensembl_gene_id":"ENSG00000111752.10","gene_symbol":"PHC1","gene_name":"polyhomeotic homolog 1 [Source:HGNC Symbol;Acc:HGNC:3182]","synonyms":"RAE28,HPH1,EDR1","biotype":"protein_coding","ncbi_id":"1911","summary":"This gene is a homolog of the Drosophila polyhomeotic gene, which is a member of the Polycomb group of genes. The gene product is a component of a multimeric protein complex that contains EDR2 and the vertebrate Polycomb protein BMH1. The gene product, the EDR2 protein, and the Drosophila polyhomeotic protein share 2 highly conserved domains, named homology domains I and II. These domains are involved in protein-protein interactions and may mediate heterodimerization of the protein encoded by this gene and the EDR2 protein. [provided by RefSeq, Jul 2008]","start":8913896,"end":8941467,"strand":1,"description":"polyhomeotic homolog 1 [Source:HGNC Symbol;Acc:HGNC:3182]"}, {"versioned_ensembl_gene_id":"ENSG00000279005.1","gene_symbol":"AC211433.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74633510,"end":74633884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271248.1","gene_symbol":"AC091193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5455218,"end":5455665,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265380.1","gene_symbol":"AC079070.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73711329,"end":73715490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241200.1","gene_symbol":"ZNF736P7Y","gene_name":"zinc finger protein 736 pseudogene 7, Y-linked [Source:HGNC Symbol;Acc:HGNC:38404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419725","summary":null,"start":7990987,"end":7991806,"strand":-1,"description":"zinc finger protein 736 pseudogene 7, Y-linked [Source:HGNC Symbol;Acc:HGNC:38404]"}, {"versioned_ensembl_gene_id":"ENSG00000279799.1","gene_symbol":"AC006077.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":134905235,"end":134905691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188549.12","gene_symbol":"C15orf52","gene_name":"chromosome 15 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:33488]","synonyms":"FLJ43339","biotype":"protein_coding","ncbi_id":"388115","summary":null,"start":40331452,"end":40340967,"strand":-1,"description":"chromosome 15 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:33488]"}, {"versioned_ensembl_gene_id":"ENSG00000274159.1","gene_symbol":"AL133243.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32548675,"end":32549040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115760.13","gene_symbol":"BIRC6","gene_name":"baculoviral IAP repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:13516]","synonyms":"BRUCE","biotype":"protein_coding","ncbi_id":"57448","summary":"This gene encodes a protein with a BIR (baculoviral inhibition of apoptosis protein repeat) domain and a UBCc (ubiquitin-conjugating enzyme E2, catalytic) domain. This protein inhibits apoptosis by facilitating the degradation of apoptotic proteins by ubiquitination. [provided by RefSeq, Jul 2008]","start":32357028,"end":32618899,"strand":1,"description":"baculoviral IAP repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:13516]"}, {"versioned_ensembl_gene_id":"ENSG00000276334.1","gene_symbol":"AL133243.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32521927,"end":32523547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270754.1","gene_symbol":"NEK4P3","gene_name":"NIMA-related kinase 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39651]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421728","summary":null,"start":65054460,"end":65055003,"strand":1,"description":"NIMA-related kinase 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39651]"}, {"versioned_ensembl_gene_id":"ENSG00000272613.1","gene_symbol":"CR759954.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861407,"end":28862038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123374.10","gene_symbol":"CDK2","gene_name":"cyclin dependent kinase 2 [Source:HGNC Symbol;Acc:HGNC:1771]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1017","summary":"This gene encodes a member of a family of serine/threonine protein kinases that participate in cell cycle regulation. The encoded protein is the catalytic subunit of the cyclin-dependent protein kinase complex, which regulates progression through the cell cycle. Activity of this protein is especially critical during the G1 to S phase transition. This protein associates with and regulated by other subunits of the complex including cyclin A or E, CDK inhibitor p21Cip1 (CDKN1A), and p27Kip1 (CDKN1B). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":55966769,"end":55972784,"strand":1,"description":"cyclin dependent kinase 2 [Source:HGNC Symbol;Acc:HGNC:1771]"}, {"versioned_ensembl_gene_id":"ENSG00000168918.13","gene_symbol":"INPP5D","gene_name":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]","synonyms":"SHIP,hp51CN,SHIP1","biotype":"protein_coding","ncbi_id":"3635","summary":"This gene is a member of the inositol polyphosphate-5-phosphatase (INPP5) family and encodes a protein with an N-terminal SH2 domain, an inositol phosphatase domain, and two C-terminal protein interaction domains. Expression of this protein is restricted to hematopoietic cells where its movement from the cytosol to the plasma membrane is mediated by tyrosine phosphorylation. At the plasma membrane, the protein hydrolyzes the 5' phosphate from phosphatidylinositol (3,4,5)-trisphosphate and inositol-1,3,4,5-tetrakisphosphate, thereby affecting multiple signaling pathways. The protein is also partly localized to the nucleus, where it may be involved in nuclear inositol phosphate signaling processes. Overall, the protein functions as a negative regulator of myeloid cell proliferation and survival. Mutations in this gene are associated with defects and cancers of the immune system. Deficiencies in the encoded protein, SHIP1, have been associated with Inflammatory Bowel Disease types such as Crohn's Disease and Ulcerative Colitis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":233059967,"end":233207903,"strand":1,"description":"inositol polyphosphate-5-phosphatase D [Source:HGNC Symbol;Acc:HGNC:6079]"}, {"versioned_ensembl_gene_id":"ENSG00000255146.1","gene_symbol":"AP004247.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58044110,"end":58060138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211689.7","gene_symbol":"TRGC1","gene_name":"T-cell receptor gamma constant 1 [Source:HGNC Symbol;Acc:HGNC:12275]","synonyms":"TCRGC1,C1","biotype":"TR_C_gene","ncbi_id":"6966","summary":null,"start":38257879,"end":38265678,"strand":-1,"description":"T-cell receptor gamma constant 1 [Source:HGNC Symbol;Acc:HGNC:12275]"}, {"versioned_ensembl_gene_id":"ENSG00000227203.3","gene_symbol":"SUB1P1","gene_name":"SUB1 homolog, transcriptional regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728938","summary":null,"start":11790005,"end":11790386,"strand":1,"description":"SUB1 homolog, transcriptional regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32300]"}, {"versioned_ensembl_gene_id":"ENSG00000222014.5","gene_symbol":"RAB6C","gene_name":"RAB6C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16525]","synonyms":"WTH3","biotype":"protein_coding","ncbi_id":"84084","summary":null,"start":129979664,"end":129982738,"strand":1,"description":"RAB6C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16525]"}, {"versioned_ensembl_gene_id":"ENSG00000237037.9","gene_symbol":"NDUFA6-AS1","gene_name":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100132273","summary":null,"start":42090931,"end":42137742,"strand":1,"description":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]"}, {"versioned_ensembl_gene_id":"ENSG00000273258.1","gene_symbol":"AC016737.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174011856,"end":174012975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232128.1","gene_symbol":"MTCO3P45","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52148]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075218","summary":null,"start":94900990,"end":94901602,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52148]"}, {"versioned_ensembl_gene_id":"ENSG00000249662.5","gene_symbol":"LINC02218","gene_name":"long intergenic non-protein coding RNA 2218 [Source:HGNC Symbol;Acc:HGNC:53085]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723526","summary":null,"start":17444010,"end":17483946,"strand":1,"description":"long intergenic non-protein coding RNA 2218 [Source:HGNC Symbol;Acc:HGNC:53085]"}, {"versioned_ensembl_gene_id":"ENSG00000255307.1","gene_symbol":"OR52B2","gene_name":"olfactory receptor family 52 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:15207]","synonyms":null,"biotype":"protein_coding","ncbi_id":"255725","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6169330,"end":6170408,"strand":-1,"description":"olfactory receptor family 52 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:15207]"}, {"versioned_ensembl_gene_id":"ENSG00000244625.5","gene_symbol":"MIATNB","gene_name":"MIAT neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50731]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724827","summary":null,"start":26672767,"end":26780207,"strand":1,"description":"MIAT neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50731]"}, {"versioned_ensembl_gene_id":"ENSG00000254444.1","gene_symbol":"AC022762.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":6108135,"end":6185576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180909.2","gene_symbol":"OR52B1P","gene_name":"olfactory receptor family 52 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15206]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81274","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6151641,"end":6152549,"strand":-1,"description":"olfactory receptor family 52 subfamily B member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15206]"}, {"versioned_ensembl_gene_id":"ENSG00000180919.3","gene_symbol":"OR56B4","gene_name":"olfactory receptor family 56 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:15248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"196335","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6107684,"end":6108835,"strand":1,"description":"olfactory receptor family 56 subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:15248]"}, {"versioned_ensembl_gene_id":"ENSG00000180714.3","gene_symbol":"OR5AZ1P","gene_name":"olfactory receptor family 5 subfamily AZ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15262]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"283193","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57917297,"end":57918239,"strand":-1,"description":"olfactory receptor family 5 subfamily AZ member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15262]"}, {"versioned_ensembl_gene_id":"ENSG00000282092.1","gene_symbol":"MED16","gene_name":"mediator complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:17556]","synonyms":"DRIP92,TRAP95,THRAP5","biotype":"protein_coding","ncbi_id":"10025","summary":null,"start":868013,"end":881626,"strand":-1,"description":"mediator complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:17556]"}, {"versioned_ensembl_gene_id":"ENSG00000226621.1","gene_symbol":"AC083855.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11290406,"end":11290663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224482.1","gene_symbol":"HSFY4P","gene_name":"heat shock transcription factor, Y-linked 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:37721]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643987","summary":null,"start":20808776,"end":20811809,"strand":-1,"description":"heat shock transcription factor, Y-linked 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:37721]"}, {"versioned_ensembl_gene_id":"ENSG00000134438.9","gene_symbol":"RAX","gene_name":"retina and anterior neural fold homeobox [Source:HGNC Symbol;Acc:HGNC:18662]","synonyms":"RX","biotype":"protein_coding","ncbi_id":"30062","summary":"This gene encodes a homeobox-containing transcription factor that functions in eye development. The gene is expressed early in the eye primordia, and is required for retinal cell fate determination and also regulates stem cell proliferation. Mutations in this gene have been reported in patients with defects in ocular development, including microphthalmia, anophthalmia, and coloboma.[provided by RefSeq, Oct 2009]","start":59267035,"end":59274086,"strand":-1,"description":"retina and anterior neural fold homeobox [Source:HGNC Symbol;Acc:HGNC:18662]"}, {"versioned_ensembl_gene_id":"ENSG00000254488.1","gene_symbol":"AC007876.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21038289,"end":21044724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233441.6","gene_symbol":"CYP2AB1P","gene_name":"cytochrome P450 family 2 subfamily AB member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39975]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"647265","summary":null,"start":183895900,"end":183910936,"strand":-1,"description":"cytochrome P450 family 2 subfamily AB member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:39975]"}, {"versioned_ensembl_gene_id":"ENSG00000196564.4","gene_symbol":"AL096700.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18838709,"end":18839452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249795.1","gene_symbol":"AC097462.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127498327,"end":127498807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129514.5","gene_symbol":"FOXA1","gene_name":"forkhead box A1 [Source:HGNC Symbol;Acc:HGNC:5021]","synonyms":"HNF3A","biotype":"protein_coding","ncbi_id":"3169","summary":"This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific transcripts such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. [provided by RefSeq, Jul 2008]","start":37589984,"end":37596059,"strand":-1,"description":"forkhead box A1 [Source:HGNC Symbol;Acc:HGNC:5021]"}, {"versioned_ensembl_gene_id":"ENSG00000143924.18","gene_symbol":"EML4","gene_name":"echinoderm microtubule associated protein like 4 [Source:HGNC Symbol;Acc:HGNC:1316]","synonyms":"ROPP120,ELP120,C2orf2","biotype":"protein_coding","ncbi_id":"27436","summary":"This gene is a member of the echinoderm microtubule associated protein-like family. The encoded WD-repeat protein may be involved in microtubule formation. Abnormal fusion of parts of this gene with portions of the anaplastic lymphoma receptor tyrosine kinase gene, which generates EML4-ALK fusion transcripts, is one of the primary mutations associated with non-small cell lung cancer. Alternative splicing of this gene results in two transcript variants. [provided by RefSeq, Jan 2015]","start":42169350,"end":42332548,"strand":1,"description":"echinoderm microtubule associated protein like 4 [Source:HGNC Symbol;Acc:HGNC:1316]"}, {"versioned_ensembl_gene_id":"ENSG00000147118.11","gene_symbol":"ZNF182","gene_name":"zinc finger protein 182 [Source:HGNC Symbol;Acc:HGNC:13001]","synonyms":"ZNF21,Zfp182,KOX14,HHZ150","biotype":"protein_coding","ncbi_id":"7569","summary":"Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, May 2010]","start":47974851,"end":48003978,"strand":-1,"description":"zinc finger protein 182 [Source:HGNC Symbol;Acc:HGNC:13001]"}, {"versioned_ensembl_gene_id":"ENSG00000213739.3","gene_symbol":"AC007679.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205949091,"end":205950145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155974.11","gene_symbol":"GRIP1","gene_name":"glutamate receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23426","summary":"This gene encodes a member of the glutamate receptor interacting protein family. The encoded scaffold protein binds to and mediates the trafficking and membrane organization of a number of transmembrane proteins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]","start":66347431,"end":66804186,"strand":-1,"description":"glutamate receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18708]"}, {"versioned_ensembl_gene_id":"ENSG00000272754.1","gene_symbol":"AL133245.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32321638,"end":32323002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237321.1","gene_symbol":"AL354936.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123823240,"end":123829285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244067.2","gene_symbol":"GSTA2","gene_name":"glutathione S-transferase alpha 2 [Source:HGNC Symbol;Acc:HGNC:4627]","synonyms":"GST2","biotype":"protein_coding","ncbi_id":"2939","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. These enzymes function in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding these enzymes are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of some drugs. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-tranferase belonging to the alpha class. The alpha class genes, located in a cluster mapped to chromosome 6, are the most abundantly expressed glutathione S-transferases in liver. In addition to metabolizing bilirubin and certain anti-cancer drugs in the liver, the alpha class of these enzymes exhibit glutathione peroxidase activity thereby protecting the cells from reactive oxygen species and the products of peroxidation. [provided by RefSeq, Jul 2008]","start":52750089,"end":52763569,"strand":-1,"description":"glutathione S-transferase alpha 2 [Source:HGNC Symbol;Acc:HGNC:4627]"}, {"versioned_ensembl_gene_id":"ENSG00000164291.16","gene_symbol":"ARSK","gene_name":"arylsulfatase family member K [Source:HGNC Symbol;Acc:HGNC:25239]","synonyms":"TSULF,DKFZp313G1735","biotype":"protein_coding","ncbi_id":"153642","summary":"Sulfatases (EC 3.1.5.6), such as ARSK, hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules (Sardiello et al., 2005 [PubMed 16174644]).[supplied by OMIM, Mar 2008]","start":95555074,"end":95605064,"strand":1,"description":"arylsulfatase family member K [Source:HGNC Symbol;Acc:HGNC:25239]"}, {"versioned_ensembl_gene_id":"ENSG00000228721.1","gene_symbol":"AC016909.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132911096,"end":132911261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186204.14","gene_symbol":"CYP4F12","gene_name":"cytochrome P450 family 4 subfamily F member 12 [Source:HGNC Symbol;Acc:HGNC:18857]","synonyms":null,"biotype":"protein_coding","ncbi_id":"66002","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein likely localizes to the endoplasmic reticulum. When expressed in yeast the enzyme is capable of oxdizing arachidonic acid. It can also catalyze the epoxidation of 22:6n-3 and 22:5n-3 polyunsaturated long-chain fatty acids. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":15672757,"end":15697174,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 12 [Source:HGNC Symbol;Acc:HGNC:18857]"}, {"versioned_ensembl_gene_id":"ENSG00000233012.2","gene_symbol":"HDAC1P2","gene_name":"histone deacetylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45191]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100419489","summary":null,"start":220625740,"end":220628056,"strand":1,"description":"histone deacetylase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45191]"}, {"versioned_ensembl_gene_id":"ENSG00000040487.12","gene_symbol":"PQLC2","gene_name":"PQ loop repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:26001]","synonyms":"FLJ20320","biotype":"protein_coding","ncbi_id":"54896","summary":null,"start":19312326,"end":19329300,"strand":1,"description":"PQ loop repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:26001]"}, {"versioned_ensembl_gene_id":"ENSG00000217085.2","gene_symbol":"HMGB3P19","gene_name":"high mobility group box 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39311]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729635","summary":null,"start":153938433,"end":153938992,"strand":-1,"description":"high mobility group box 3 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39311]"}, {"versioned_ensembl_gene_id":"ENSG00000235147.1","gene_symbol":"AC128677.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92006680,"end":92007121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218776.4","gene_symbol":"MTATP6P31","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52186]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075205","summary":null,"start":153666627,"end":153667318,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52186]"}, {"versioned_ensembl_gene_id":"ENSG00000275025.1","gene_symbol":"AC002401.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50098460,"end":50098899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165023.6","gene_symbol":"DIRAS2","gene_name":"DIRAS family GTPase 2 [Source:HGNC Symbol;Acc:HGNC:19323]","synonyms":"DKFZp761C07121,Di-Ras2","biotype":"protein_coding","ncbi_id":"54769","summary":"DIRAS2 belongs to a distinct branch of the functionally diverse Ras (see HRAS; MIM 190020) superfamily of monomeric GTPases.[supplied by OMIM, Apr 2004]","start":90609832,"end":90643105,"strand":-1,"description":"DIRAS family GTPase 2 [Source:HGNC Symbol;Acc:HGNC:19323]"}, {"versioned_ensembl_gene_id":"ENSG00000175582.19","gene_symbol":"RAB6A","gene_name":"RAB6A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9786]","synonyms":"RAB6","biotype":"protein_coding","ncbi_id":"5870","summary":"This gene encodes a member of the RAB family, which belongs to the small GTPase superfamily. GTPases of the RAB family bind to various effectors to regulate the targeting and fusion of transport carriers to acceptor compartments. This protein is located at the Golgi apparatus, which regulates trafficking in both a retrograde (from early endosomes and Golgi to the endoplasmic reticulum) and an anterograde (from the Golgi to the plasma membrane) directions. Myosin II is an effector of this protein in these processes. This protein is also involved in assembly of human cytomegalovirus (HCMV) by interacting with the cellular protein Bicaudal D1, which interacts with the HCMV virion tegument protein, pp150. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":73675638,"end":73761137,"strand":-1,"description":"RAB6A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9786]"}, {"versioned_ensembl_gene_id":"ENSG00000234362.5","gene_symbol":"LINC01914","gene_name":"long intergenic non-protein coding RNA 1914 [Source:HGNC Symbol;Acc:HGNC:52733]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929723","summary":null,"start":41931599,"end":41933723,"strand":-1,"description":"long intergenic non-protein coding RNA 1914 [Source:HGNC Symbol;Acc:HGNC:52733]"}, {"versioned_ensembl_gene_id":"ENSG00000274261.1","gene_symbol":"AL137078.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48407367,"end":48410716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231231.5","gene_symbol":"LINC01423","gene_name":"long intergenic non-protein coding RNA 1423 [Source:HGNC Symbol;Acc:HGNC:50732]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724678","summary":null,"start":38323635,"end":38333421,"strand":-1,"description":"long intergenic non-protein coding RNA 1423 [Source:HGNC Symbol;Acc:HGNC:50732]"}, {"versioned_ensembl_gene_id":"ENSG00000226226.1","gene_symbol":"PRELID3BP1","gene_name":"PRELI domain containing 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49063]","synonyms":"SLMO2P1","biotype":"processed_pseudogene","ncbi_id":"100129664","summary":null,"start":220467954,"end":220468808,"strand":1,"description":"PRELI domain containing 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49063]"}, {"versioned_ensembl_gene_id":"ENSG00000258586.1","gene_symbol":"LINC02274","gene_name":"long intergenic non-protein coding RNA 2274 [Source:HGNC Symbol;Acc:HGNC:53190]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506498","summary":null,"start":73822559,"end":73830135,"strand":-1,"description":"long intergenic non-protein coding RNA 2274 [Source:HGNC Symbol;Acc:HGNC:53190]"}, {"versioned_ensembl_gene_id":"ENSG00000236874.1","gene_symbol":"AL137078.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48383323,"end":48384895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225073.10","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"BAT1,UAP56,D6S81E","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31517671,"end":31534027,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000254887.1","gene_symbol":"AC010247.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":42132555,"end":42137099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260409.1","gene_symbol":"AC012414.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20729747,"end":20756183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223991.1","gene_symbol":"AC104809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":240981515,"end":240986072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204818.4","gene_symbol":"ADGRF5P2","gene_name":"adhesion G protein-coupled receptor F5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32921]","synonyms":"GPR116P2","biotype":"unprocessed_pseudogene","ncbi_id":"441416","summary":null,"start":42795392,"end":42800672,"strand":1,"description":"adhesion G protein-coupled receptor F5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32921]"}, {"versioned_ensembl_gene_id":"ENSG00000271526.1","gene_symbol":"AC004852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9084022,"end":9084175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228293.1","gene_symbol":"AL049712.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2664352,"end":2665874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257271.1","gene_symbol":"KIRREL3-AS1","gene_name":"KIRREL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42655]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874250","summary":null,"start":126543947,"end":126610948,"strand":1,"description":"KIRREL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42655]"}, {"versioned_ensembl_gene_id":"ENSG00000218109.5","gene_symbol":"KIRREL3-AS3","gene_name":"KIRREL3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:26855]","synonyms":"PRR10,NCRNA00288,FLJ40224","biotype":"antisense_RNA","ncbi_id":"283165","summary":null,"start":127002910,"end":127006058,"strand":1,"description":"KIRREL3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:26855]"}, {"versioned_ensembl_gene_id":"ENSG00000123595.7","gene_symbol":"RAB9A","gene_name":"RAB9A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9792]","synonyms":"RAB9","biotype":"protein_coding","ncbi_id":"9367","summary":null,"start":13689125,"end":13710506,"strand":1,"description":"RAB9A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9792]"}, {"versioned_ensembl_gene_id":"ENSG00000229461.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29809470,"end":29809601,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000260711.2","gene_symbol":"AL121839.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":91752856,"end":91759798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267135.2","gene_symbol":"AD000091.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15611623,"end":15611909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248532.2","gene_symbol":"AC119751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49523648,"end":49523857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175048.16","gene_symbol":"ZDHHC14","gene_name":"zinc finger DHHC-type containing 14 [Source:HGNC Symbol;Acc:HGNC:20341]","synonyms":"NEW1CP,FLJ20984","biotype":"protein_coding","ncbi_id":"79683","summary":null,"start":157381133,"end":157678146,"strand":1,"description":"zinc finger DHHC-type containing 14 [Source:HGNC Symbol;Acc:HGNC:20341]"}, {"versioned_ensembl_gene_id":"ENSG00000231875.1","gene_symbol":"AL359885.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81363268,"end":81364170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280815.1","gene_symbol":"OR2AS2P","gene_name":"olfactory receptor family 2 subfamily AS member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31248]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403236","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248500752,"end":248501072,"strand":1,"description":"olfactory receptor family 2 subfamily AS member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31248]"}, {"versioned_ensembl_gene_id":"ENSG00000253711.1","gene_symbol":"AC023866.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61300164,"end":61301069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262517.1","gene_symbol":"AL035045.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17814608,"end":17815038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253137.1","gene_symbol":"AC092709.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84678798,"end":84679842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100122.5","gene_symbol":"CRYBB1","gene_name":"crystallin beta B1 [Source:HGNC Symbol;Acc:HGNC:2397]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1414","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta basic group member, undergoes extensive cleavage at its N-terminal extension during lens maturation. It is also a member of a gene cluster with beta-A4, beta-B2, and beta-B3. [provided by RefSeq, Jul 2008]","start":26599278,"end":26618088,"strand":-1,"description":"crystallin beta B1 [Source:HGNC Symbol;Acc:HGNC:2397]"}, {"versioned_ensembl_gene_id":"ENSG00000279557.1","gene_symbol":"AC010435.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":43586367,"end":43587543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228174.7","gene_symbol":"AL162385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97512706,"end":97517836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224993.3","gene_symbol":"RPL29P12","gene_name":"ribosomal protein L29 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36608]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283412","summary":null,"start":43666766,"end":43667232,"strand":-1,"description":"ribosomal protein L29 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36608]"}, {"versioned_ensembl_gene_id":"ENSG00000226927.1","gene_symbol":"AL451081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220359731,"end":220360183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135222.6","gene_symbol":"CSN2","gene_name":"casein beta [Source:HGNC Symbol;Acc:HGNC:2447]","synonyms":"CASB","biotype":"protein_coding","ncbi_id":"1447","summary":"This gene is a member of the beta casein family. There are two types of casein protein, beta (encoded by this gene) and kappa, both of which are secreted in human milk. Beta casein is the principal protein in human milk and the primary source of essential amino acids for a suckling infant. Beta and kappa casein proteins acting together form spherical micelles which bind within them important dietary minerals, such as calcium and phosphorous. In addition, the C-terminal 14 aa of the protein has antimicrobial activity, especially in preterm milk, displaying antibacterial activity against S. aureus and Y. enterocolitica. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":69955256,"end":69961007,"strand":-1,"description":"casein beta [Source:HGNC Symbol;Acc:HGNC:2447]"}, {"versioned_ensembl_gene_id":"ENSG00000174572.3","gene_symbol":"RPL10P2","gene_name":"ribosomal protein L10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13975]","synonyms":"RPL10p,bA209A2.1","biotype":"processed_pseudogene","ncbi_id":"442171","summary":null,"start":27211244,"end":27211913,"strand":1,"description":"ribosomal protein L10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13975]"}, {"versioned_ensembl_gene_id":"ENSG00000270390.1","gene_symbol":"AC013444.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142947300,"end":142948086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236287.7","gene_symbol":"ZBED5","gene_name":"zinc finger BED-type containing 5 [Source:HGNC Symbol;Acc:HGNC:30803]","synonyms":"Buster1","biotype":"protein_coding","ncbi_id":"58486","summary":"This gene is unusual in that its coding sequence is mostly derived from Charlie-like DNA transposon; however, it does not appear to be an active DNA transposon as it is not flanked by terminal inverted repeats. The encoded protein is conserved among the mammalian Laurasiatheria branch. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2009]","start":10812074,"end":10858796,"strand":-1,"description":"zinc finger BED-type containing 5 [Source:HGNC Symbol;Acc:HGNC:30803]"}, {"versioned_ensembl_gene_id":"ENSG00000215704.9","gene_symbol":"CELA2B","gene_name":"chymotrypsin like elastase family member 2B [Source:HGNC Symbol;Acc:HGNC:29995]","synonyms":"RP11-265F14.2,ELA2B","biotype":"protein_coding","ncbi_id":"51032","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Like most of the human elastases, elastase 2B is secreted from the pancreas as a zymogen. In other species, elastase 2B has been shown to preferentially cleave proteins after leucine, methionine, and phenylalanine residues. [provided by RefSeq, Jul 2008]","start":15465909,"end":15491400,"strand":1,"description":"chymotrypsin like elastase family member 2B [Source:HGNC Symbol;Acc:HGNC:29995]"}, {"versioned_ensembl_gene_id":"ENSG00000271966.1","gene_symbol":"AC021321.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67343975,"end":67345087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224473.1","gene_symbol":"CCND3P1","gene_name":"cyclin D3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1586]","synonyms":"CCND3P","biotype":"processed_pseudogene","ncbi_id":"897","summary":null,"start":30403197,"end":30403776,"strand":-1,"description":"cyclin D3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1586]"}, {"versioned_ensembl_gene_id":"ENSG00000185074.7","gene_symbol":"OR7E31P","gene_name":"olfactory receptor family 7 subfamily E member 31 pseudogene [Source:HGNC Symbol;Acc:HGNC:8404]","synonyms":"OST205,OR7E32P","biotype":"unprocessed_pseudogene","ncbi_id":"375601","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":90216039,"end":90216924,"strand":1,"description":"olfactory receptor family 7 subfamily E member 31 pseudogene [Source:HGNC Symbol;Acc:HGNC:8404]"}, {"versioned_ensembl_gene_id":"ENSG00000231188.1","gene_symbol":"AL139819.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100335563,"end":100346390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217769.4","gene_symbol":"AL157777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86897118,"end":86897421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218561.1","gene_symbol":"AL353133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86729708,"end":86730108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274853.2","gene_symbol":"MRM1","gene_name":"mitochondrial rRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26202]","synonyms":"FLJ22578","biotype":"protein_coding","ncbi_id":"79922","summary":null,"start":36602534,"end":36609940,"strand":1,"description":"mitochondrial rRNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26202]"}, {"versioned_ensembl_gene_id":"ENSG00000105122.12","gene_symbol":"RASAL3","gene_name":"RAS protein activator like 3 [Source:HGNC Symbol;Acc:HGNC:26129]","synonyms":"FLJ21438","biotype":"protein_coding","ncbi_id":"64926","summary":"This gene belongs to the Ras GTPase-activating proteins (RasGAP) family and encodes a protein with pleckstrin homology (PH), C2, and Ras GTPase-activation protein (RasGAP) domains. This protein is localized near or at the plasma membrane when expressed exogenously. Reduced expression of this gene in some cell lines resulted in increased levels of the active form of Ras (Ras-GTP), suggesting that this gene may play a role in negatively regulating the Ras signaling pathway. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]","start":15451624,"end":15464571,"strand":-1,"description":"RAS protein activator like 3 [Source:HGNC Symbol;Acc:HGNC:26129]"}, {"versioned_ensembl_gene_id":"ENSG00000130222.10","gene_symbol":"GADD45G","gene_name":"growth arrest and DNA damage inducible gamma [Source:HGNC Symbol;Acc:HGNC:4097]","synonyms":"GRP17,GADD45gamma,DDIT2,CR6","biotype":"protein_coding","ncbi_id":"10912","summary":"This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The protein encoded by this gene responds to environmental stresses by mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The GADD45G is highly expressed in placenta. [provided by RefSeq, Jul 2008]","start":89605013,"end":89606555,"strand":1,"description":"growth arrest and DNA damage inducible gamma [Source:HGNC Symbol;Acc:HGNC:4097]"}, {"versioned_ensembl_gene_id":"ENSG00000261886.1","gene_symbol":"AC005670.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46916770,"end":46923034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121057.12","gene_symbol":"AKAP1","gene_name":"A-kinase anchoring protein 1 [Source:HGNC Symbol;Acc:HGNC:367]","synonyms":"AKAP121,TDRD17,SAKAP84,S-AKAP84,PRKA1,PPP1R43,D-AKAP1,AKAP84,AKAP149","biotype":"protein_coding","ncbi_id":"8165","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein binds to type I and type II regulatory subunits of PKA and anchors them to the mitochondrion. This protein is speculated to be involved in the cAMP-dependent signal transduction pathway and in directing RNA to a specific cellular compartment. [provided by RefSeq, Jul 2008]","start":57085092,"end":57121349,"strand":1,"description":"A-kinase anchoring protein 1 [Source:HGNC Symbol;Acc:HGNC:367]"}, {"versioned_ensembl_gene_id":"ENSG00000262904.1","gene_symbol":"TMPOP2","gene_name":"thymopoietin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50860]","synonyms":"lncRNA-EBIC","biotype":"processed_pseudogene","ncbi_id":"100533619","summary":null,"start":74667506,"end":74668706,"strand":1,"description":"thymopoietin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50860]"}, {"versioned_ensembl_gene_id":"ENSG00000262640.1","gene_symbol":"AC207480.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17872581,"end":17878345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254222.1","gene_symbol":"AC023866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61264624,"end":61292039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254285.3","gene_symbol":"KRT8P3","gene_name":"keratin 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728638","summary":null,"start":61578220,"end":61579668,"strand":1,"description":"keratin 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31056]"}, {"versioned_ensembl_gene_id":"ENSG00000184672.11","gene_symbol":"RALYL","gene_name":"RALY RNA binding protein like [Source:HGNC Symbol;Acc:HGNC:27036]","synonyms":"HNRPCL3","biotype":"protein_coding","ncbi_id":"138046","summary":null,"start":84182787,"end":84921844,"strand":1,"description":"RALY RNA binding protein like [Source:HGNC Symbol;Acc:HGNC:27036]"}, {"versioned_ensembl_gene_id":"ENSG00000211728.2","gene_symbol":"TRBV5-6","gene_name":"T-cell receptor beta variable 5-6 [Source:HGNC Symbol;Acc:HGNC:12223]","synonyms":"TRBV56,TCRBV5S6,TCRBV5S2","biotype":"TR_V_gene","ncbi_id":"28609","summary":null,"start":142500028,"end":142500534,"strand":1,"description":"T-cell receptor beta variable 5-6 [Source:HGNC Symbol;Acc:HGNC:12223]"}, {"versioned_ensembl_gene_id":"ENSG00000262802.1","gene_symbol":"AL035045.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17893379,"end":17894176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259554.1","gene_symbol":"AC084882.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47274183,"end":47275164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261419.1","gene_symbol":"AC145285.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28659696,"end":28740781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259221.5","gene_symbol":"AC023905.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47359430,"end":47396732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237438.7","gene_symbol":"CECR7","gene_name":"cat eye syndrome chromosome region, candidate 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1845]","synonyms":"SAHL1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100130418","summary":null,"start":17036570,"end":17060825,"strand":1,"description":"cat eye syndrome chromosome region, candidate 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:1845]"}, {"versioned_ensembl_gene_id":"ENSG00000198363.17","gene_symbol":"ASPH","gene_name":"aspartate beta-hydroxylase [Source:HGNC Symbol;Acc:HGNC:757]","synonyms":"JCTN,HAAH,CASQ2BP1,BAH","biotype":"protein_coding","ncbi_id":"444","summary":"This gene is thought to play an important role in calcium homeostasis. The gene is expressed from two promoters and undergoes extensive alternative splicing. The encoded set of proteins share varying amounts of overlap near their N-termini but have substantial variations in their C-terminal domains resulting in distinct functional properties. The longest isoforms (a and f) include a C-terminal Aspartyl/Asparaginyl beta-hydroxylase domain that hydroxylates aspartic acid or asparagine residues in the epidermal growth factor (EGF)-like domains of some proteins, including protein C, coagulation factors VII, IX, and X, and the complement factors C1R and C1S. Other isoforms differ primarily in the C-terminal sequence and lack the hydroxylase domain, and some have been localized to the endoplasmic and sarcoplasmic reticulum. Some of these isoforms are found in complexes with calsequestrin, triadin, and the ryanodine receptor, and have been shown to regulate calcium release from the sarcoplasmic reticulum. Some isoforms have been implicated in metastasis. [provided by RefSeq, Sep 2009]","start":61500556,"end":61714640,"strand":-1,"description":"aspartate beta-hydroxylase [Source:HGNC Symbol;Acc:HGNC:757]"}, {"versioned_ensembl_gene_id":"ENSG00000184110.14","gene_symbol":"EIF3C","gene_name":"eukaryotic translation initiation factor 3 subunit C [Source:HGNC Symbol;Acc:HGNC:3279]","synonyms":"EIF3S8,eIF3c,eIF3-p110","biotype":"protein_coding","ncbi_id":"8663","summary":null,"start":28688558,"end":28735730,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit C [Source:HGNC Symbol;Acc:HGNC:3279]"}, {"versioned_ensembl_gene_id":"ENSG00000088727.12","gene_symbol":"KIF9","gene_name":"kinesin family member 9 [Source:HGNC Symbol;Acc:HGNC:16666]","synonyms":"MGC104186","biotype":"protein_coding","ncbi_id":"64147","summary":null,"start":47228026,"end":47283451,"strand":-1,"description":"kinesin family member 9 [Source:HGNC Symbol;Acc:HGNC:16666]"}, {"versioned_ensembl_gene_id":"ENSG00000258279.3","gene_symbol":"LINC00592","gene_name":"long intergenic non-protein coding RNA 592 [Source:HGNC Symbol;Acc:HGNC:27474]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283404","summary":null,"start":52164115,"end":52223804,"strand":1,"description":"long intergenic non-protein coding RNA 592 [Source:HGNC Symbol;Acc:HGNC:27474]"}, {"versioned_ensembl_gene_id":"ENSG00000257137.6","gene_symbol":"C12orf80","gene_name":"chromosome 12 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:27473]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283403","summary":null,"start":52205556,"end":52213583,"strand":-1,"description":"chromosome 12 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:27473]"}, {"versioned_ensembl_gene_id":"ENSG00000258556.1","gene_symbol":"LINC02322","gene_name":"long intergenic non-protein coding RNA 2322 [Source:HGNC Symbol;Acc:HGNC:53241]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927729","summary":null,"start":60323236,"end":60323907,"strand":1,"description":"long intergenic non-protein coding RNA 2322 [Source:HGNC Symbol;Acc:HGNC:53241]"}, {"versioned_ensembl_gene_id":"ENSG00000123360.11","gene_symbol":"PDE1B","gene_name":"phosphodiesterase 1B [Source:HGNC Symbol;Acc:HGNC:8775]","synonyms":"PDES1B","biotype":"protein_coding","ncbi_id":"5153","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE1 subfamily. Members of the PDE1 family are calmodulin-dependent PDEs that are stimulated by a calcium-calmodulin complex. This PDE has dual-specificity for the second messengers, cAMP and cGMP, with a preference for cGMP as a substrate. cAMP and cGMP function as key regulators of many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":54549350,"end":54579239,"strand":1,"description":"phosphodiesterase 1B [Source:HGNC Symbol;Acc:HGNC:8775]"}, {"versioned_ensembl_gene_id":"ENSG00000108691.9","gene_symbol":"CCL2","gene_name":"C-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:10618]","synonyms":"SMC-CF,SCYA2,MGC9434,MCP1,MCP-1,MCAF,HC11,GDCF-2","biotype":"protein_coding","ncbi_id":"6347","summary":"This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Chemokines are a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of N-terminal cysteine residues of the mature peptide. This chemokine is a member of the CC subfamily which is characterized by two adjacent cysteine residues. This cytokine displays chemotactic activity for monocytes and basophils but not for neutrophils or eosinophils. It has been implicated in the pathogenesis of diseases characterized by monocytic infiltrates, like psoriasis, rheumatoid arthritis and atherosclerosis. It binds to chemokine receptors CCR2 and CCR4. Elevated expression of the encoded protein is associated with severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection. [provided by RefSeq, Aug 2020]","start":34255218,"end":34257203,"strand":1,"description":"C-C motif chemokine ligand 2 [Source:HGNC Symbol;Acc:HGNC:10618]"}, {"versioned_ensembl_gene_id":"ENSG00000184500.14","gene_symbol":"PROS1","gene_name":"protein S (alpha) [Source:HGNC Symbol;Acc:HGNC:9456]","synonyms":"PROS","biotype":"protein_coding","ncbi_id":"5627","summary":"This gene encodes a vitamin K-dependent plasma protein that functions as a cofactor for the anticoagulant protease, activated protein C (APC) to inhibit blood coagulation. It is found in plasma in both a free, functionally active form and also in an inactive form complexed with C4b-binding protein. Mutations in this gene result in autosomal dominant hereditary thrombophilia. An inactive pseudogene of this locus is located at an adjacent region on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Oct 2015]","start":93873033,"end":93974066,"strand":-1,"description":"protein S (alpha) [Source:HGNC Symbol;Acc:HGNC:9456]"}, {"versioned_ensembl_gene_id":"ENSG00000137872.16","gene_symbol":"SEMA6D","gene_name":"semaphorin 6D [Source:HGNC Symbol;Acc:HGNC:16770]","synonyms":"KIAA1479,FLJ11598","biotype":"protein_coding","ncbi_id":"80031","summary":"Semaphorins are a large family, including both secreted and membrane associated proteins, many of which have been implicated as inhibitors or chemorepellents in axon pathfinding, fasciculation and branching, and target selection. All semaphorins possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Additional sequence motifs C-terminal to the semaphorin domain allow classification into distinct subfamilies. Results demonstrate that transmembrane semaphorins, like the secreted ones, can act as repulsive axon guidance cues. This gene encodes a class 6 vertebrate transmembrane semaphorin that demonstrates alternative splicing. Several transcript variants have been identified and expression of the distinct encoded isoforms is thought to be regulated in a tissue- and development-dependent manner. [provided by RefSeq, Nov 2010]","start":47184101,"end":47774223,"strand":1,"description":"semaphorin 6D [Source:HGNC Symbol;Acc:HGNC:16770]"}, {"versioned_ensembl_gene_id":"ENSG00000167767.13","gene_symbol":"KRT80","gene_name":"keratin 80 [Source:HGNC Symbol;Acc:HGNC:27056]","synonyms":"KB20","biotype":"protein_coding","ncbi_id":"144501","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene's expression profile shows that it encodes a type II epithelial keratin, although structurally the encoded protein is more like a type II hair keratin. This protein is involved in cell differentiation, localizing near desmosomal plaques in earlier stages of differentiation but then dispersing throughout the cytoplasm in terminally differentiating cells. The type II keratins are clustered in a region of chromosome 12q13. Two transcript variants encoding two different fully functional isoforms have been found for this gene.[provided by RefSeq, Oct 2010]","start":52168996,"end":52192000,"strand":-1,"description":"keratin 80 [Source:HGNC Symbol;Acc:HGNC:27056]"}, {"versioned_ensembl_gene_id":"ENSG00000101639.18","gene_symbol":"CEP192","gene_name":"centrosomal protein 192 [Source:HGNC Symbol;Acc:HGNC:25515]","synonyms":"PPP1R62,KIAA1569,FLJ10352","biotype":"protein_coding","ncbi_id":"55125","summary":null,"start":12991362,"end":13125052,"strand":1,"description":"centrosomal protein 192 [Source:HGNC Symbol;Acc:HGNC:25515]"}, {"versioned_ensembl_gene_id":"ENSG00000235592.1","gene_symbol":"AC004674.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13327937,"end":13329867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115919.14","gene_symbol":"KYNU","gene_name":"kynureninase [Source:HGNC Symbol;Acc:HGNC:6469]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8942","summary":"Kynureninase is a pyridoxal-5'-phosphate (pyridoxal-P) dependent enzyme that catalyzes the cleavage of L-kynurenine and L-3-hydroxykynurenine into anthranilic and 3-hydroxyanthranilic acids, respectively. Kynureninase is involved in the biosynthesis of NAD cofactors from tryptophan through the kynurenine pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":142877498,"end":143055832,"strand":1,"description":"kynureninase [Source:HGNC Symbol;Acc:HGNC:6469]"}, {"versioned_ensembl_gene_id":"ENSG00000226985.5","gene_symbol":"LINC01203","gene_name":"long intergenic non-protein coding RNA 1203 [Source:HGNC Symbol;Acc:HGNC:49634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133123","summary":null,"start":13335241,"end":13373634,"strand":1,"description":"long intergenic non-protein coding RNA 1203 [Source:HGNC Symbol;Acc:HGNC:49634]"}, {"versioned_ensembl_gene_id":"ENSG00000145016.15","gene_symbol":"RUBCN","gene_name":"RUN and cysteine rich domain containing beclin 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:28991]","synonyms":"rundataxin,rubicon,KIAA0226","biotype":"protein_coding","ncbi_id":"9711","summary":"The protein encoded by this gene is a negative regulator of autophagy and endocytic trafficking and controls endosome maturation. This protein contains two conserved domains, an N-terminal RUN domain and a C-terminal DUF4206 domain. The RUN domain is involved in Ras-like GTPase signaling, and the DUF4206 domain contains a diacylglycerol (DAG) binding-like motif. Mutation in this gene results in deletion of the DAG binding-like motif and causes a recessive ataxia. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":197671393,"end":197749727,"strand":-1,"description":"RUN and cysteine rich domain containing beclin 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:28991]"}, {"versioned_ensembl_gene_id":"ENSG00000257155.1","gene_symbol":"AL163973.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31558507,"end":31561334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197582.5","gene_symbol":"GPX1P1","gene_name":"glutathione peroxidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4560]","synonyms":"GPXP1,GPXL2","biotype":"processed_pseudogene","ncbi_id":"441481","summary":null,"start":13378735,"end":13379340,"strand":-1,"description":"glutathione peroxidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4560]"}, {"versioned_ensembl_gene_id":"ENSG00000259169.1","gene_symbol":"GNRHR2P1","gene_name":"GNRHR2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39424]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"404718","summary":null,"start":60398934,"end":60400013,"strand":-1,"description":"GNRHR2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39424]"}, {"versioned_ensembl_gene_id":"ENSG00000226434.1","gene_symbol":"AC135371.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13377188,"end":13403019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179008.8","gene_symbol":"C14orf39","gene_name":"chromosome 14 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:19849]","synonyms":"SIX6OS1","biotype":"protein_coding","ncbi_id":"317761","summary":null,"start":60396469,"end":60515543,"strand":-1,"description":"chromosome 14 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:19849]"}, {"versioned_ensembl_gene_id":"ENSG00000270861.1","gene_symbol":"AP002906.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97853021,"end":97853253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151418.11","gene_symbol":"ATP6V1G3","gene_name":"ATPase H+ transporting V1 subunit G3 [Source:HGNC Symbol;Acc:HGNC:18265]","synonyms":"ATP6G3,Vma10","biotype":"protein_coding","ncbi_id":"127124","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'' and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes one of three G subunit proteins. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":198523222,"end":198540945,"strand":-1,"description":"ATPase H+ transporting V1 subunit G3 [Source:HGNC Symbol;Acc:HGNC:18265]"}, {"versioned_ensembl_gene_id":"ENSG00000237640.1","gene_symbol":"AC004522.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99929392,"end":99948620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176402.5","gene_symbol":"GJC3","gene_name":"gap junction protein gamma 3 [Source:HGNC Symbol;Acc:HGNC:17495]","synonyms":"GJE1,CX30.2","biotype":"protein_coding","ncbi_id":"349149","summary":"This gene encodes a gap junction protein. The encoded protein, also known as a connexin, plays a role in formation of gap junctions, which provide direct connections between neighboring cells. Mutations in this gene have been reported to be associated with nonsyndromic hearing loss.[provided by RefSeq, Feb 2010]","start":99923269,"end":99929620,"strand":-1,"description":"gap junction protein gamma 3 [Source:HGNC Symbol;Acc:HGNC:17495]"}, {"versioned_ensembl_gene_id":"ENSG00000262370.5","gene_symbol":"AC108134.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3076911,"end":3087100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162771.7","gene_symbol":"FAM71A","gene_name":"family with sequence similarity 71 member A [Source:HGNC Symbol;Acc:HGNC:26541]","synonyms":"FLJ32796","biotype":"protein_coding","ncbi_id":"149647","summary":"This gene encodes a protein that interacts with the Rab2B small GTPase and may be important for integrity of the Golgi body. A knockdown of this gene induces fragmentation of the Golgi, similar to the effect seen with a knockdown of the Rab2B small GTPase. The encoded protein has an N-terminal Rab-binding domain specific for Rab2B. [provided by RefSeq, Feb 2017]","start":212624474,"end":212626778,"strand":1,"description":"family with sequence similarity 71 member A [Source:HGNC Symbol;Acc:HGNC:26541]"}, {"versioned_ensembl_gene_id":"ENSG00000273442.1","gene_symbol":"AC006946.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17080701,"end":17081456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235328.1","gene_symbol":"AC006946.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17093612,"end":17093939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280641.2","gene_symbol":"CDH4","gene_name":"cadherin 4 [Source:HGNC Symbol;Acc:HGNC:1763]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1002","summary":"This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Based on studies in chicken and mouse, this cadherin is thought to play an important role during brain segmentation and neuronal outgrowth. In addition, a role in kidney and muscle development is indicated. Of particular interest are studies showing stable cis-heterodimers of cadherins 2 and 4 in cotransfected cell lines. Previously thought to interact in an exclusively homophilic manner, this is the first evidence of cadherin heterodimerization. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":61894910,"end":61940574,"strand":1,"description":"cadherin 4 [Source:HGNC Symbol;Acc:HGNC:1763]"}, {"versioned_ensembl_gene_id":"ENSG00000259307.1","gene_symbol":"PLCB2-AS1","gene_name":"PLCB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43662]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874186","summary":null,"start":40300670,"end":40301820,"strand":1,"description":"PLCB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43662]"}, {"versioned_ensembl_gene_id":"ENSG00000253639.1","gene_symbol":"SUMO2P18","gene_name":"SUMO2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49356]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481679","summary":null,"start":97858049,"end":97858947,"strand":-1,"description":"SUMO2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49356]"}, {"versioned_ensembl_gene_id":"ENSG00000231137.1","gene_symbol":"RBM22P5","gene_name":"RNA binding motif protein 22 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39698]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133206","summary":null,"start":76286494,"end":76288081,"strand":-1,"description":"RNA binding motif protein 22 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39698]"}, {"versioned_ensembl_gene_id":"ENSG00000261250.1","gene_symbol":"AL160286.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179543201,"end":179548922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162482.4","gene_symbol":"AKR7A3","gene_name":"aldo-keto reductase family 7 member A3 [Source:HGNC Symbol;Acc:HGNC:390]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22977","summary":"Aldo-keto reductases, such as AKR7A3, are involved in the detoxification of aldehydes and ketones.[supplied by OMIM, Apr 2004]","start":19282558,"end":19289250,"strand":-1,"description":"aldo-keto reductase family 7 member A3 [Source:HGNC Symbol;Acc:HGNC:390]"}, {"versioned_ensembl_gene_id":"ENSG00000231473.2","gene_symbol":"LINC00441","gene_name":"long intergenic non-protein coding RNA 441 [Source:HGNC Symbol;Acc:HGNC:42778]","synonyms":"ncRNA-RB1","biotype":"lincRNA","ncbi_id":"100862704","summary":null,"start":48296513,"end":48303661,"strand":-1,"description":"long intergenic non-protein coding RNA 441 [Source:HGNC Symbol;Acc:HGNC:42778]"}, {"versioned_ensembl_gene_id":"ENSG00000236539.3","gene_symbol":"HNRNPA1P54","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:48784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421398","summary":null,"start":179447602,"end":179457315,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:48784]"}, {"versioned_ensembl_gene_id":"ENSG00000258849.1","gene_symbol":"OR7E159P","gene_name":"olfactory receptor family 7 subfamily E member 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:31312]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403299","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":51771789,"end":51772086,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 159 pseudogene [Source:HGNC Symbol;Acc:HGNC:31312]"}, {"versioned_ensembl_gene_id":"ENSG00000258535.1","gene_symbol":"AL079307.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":51765276,"end":51825422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162779.21","gene_symbol":"AXDND1","gene_name":"axonemal dynein light chain domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26564]","synonyms":"FLJ32940,C1orf125","biotype":"protein_coding","ncbi_id":"126859","summary":null,"start":179365720,"end":179554735,"strand":1,"description":"axonemal dynein light chain domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26564]"}, {"versioned_ensembl_gene_id":"ENSG00000243504.1","gene_symbol":"RPS23P1","gene_name":"ribosomal protein S23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"93948","summary":null,"start":97865054,"end":97865485,"strand":1,"description":"ribosomal protein S23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16043]"}, {"versioned_ensembl_gene_id":"ENSG00000259157.1","gene_symbol":"AL079307.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51787461,"end":51787743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213707.2","gene_symbol":"HMGB1P10","gene_name":"high mobility group box 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:4994]","synonyms":"HMGB1L10,HMG1L10","biotype":"processed_pseudogene","ncbi_id":"100130561","summary":null,"start":26560526,"end":26561088,"strand":1,"description":"high mobility group box 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:4994]"}, {"versioned_ensembl_gene_id":"ENSG00000260917.1","gene_symbol":"AL158212.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":112823490,"end":112827726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278229.2","gene_symbol":"RPS17","gene_name":"ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:10397]","synonyms":"MGC72007,S17,RPS17L2,RPS17L1,RPS17L","biotype":"protein_coding","ncbi_id":"6218","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S17E family of ribosomal proteins and is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia 4. Alternative splicing of this gene results in multiple transcript variants. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Apr 2014]","start":82615842,"end":82619653,"strand":-1,"description":"ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:10397]"}, {"versioned_ensembl_gene_id":"ENSG00000128294.15","gene_symbol":"TPST2","gene_name":"tyrosylprotein sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:12021]","synonyms":"TANGO13B","biotype":"protein_coding","ncbi_id":"8459","summary":"The protein encoded by this gene catalyzes the O-sulfation of tyrosine residues within acidic regions of proteins. The encoded protein is a type II integral membrane protein found in the Golgi body. Alternative splicing produces multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018]","start":26521983,"end":26596717,"strand":-1,"description":"tyrosylprotein sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:12021]"}, {"versioned_ensembl_gene_id":"ENSG00000279315.1","gene_symbol":"AL158212.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":112831169,"end":112832454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259118.5","gene_symbol":"AL139022.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65082034,"end":65094212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283757.1","gene_symbol":"AL031686.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46455033,"end":46496731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225292.2","gene_symbol":"AL158212.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":112888735,"end":112906111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184617.10","gene_symbol":"ZNF840P","gene_name":"zinc finger protein 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:34344]","synonyms":"ZNF840,dJ981L23.3,C20orf157","biotype":"unprocessed_pseudogene","ncbi_id":"100533646","summary":null,"start":46484461,"end":46492640,"strand":1,"description":"zinc finger protein 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:34344]"}, {"versioned_ensembl_gene_id":"ENSG00000171811.13","gene_symbol":"CFAP46","gene_name":"cilia and flagella associated protein 46 [Source:HGNC Symbol;Acc:HGNC:25247]","synonyms":"TTC40,FLJ25954,DKFZp434A1721,C10orf93,C10orf92,C10orf124,C10orf123,bB137A17.3,bB137A17.2,bA288G11.5,bA288G11.4","biotype":"protein_coding","ncbi_id":"54777","summary":null,"start":132808392,"end":132942823,"strand":-1,"description":"cilia and flagella associated protein 46 [Source:HGNC Symbol;Acc:HGNC:25247]"}, {"versioned_ensembl_gene_id":"ENSG00000166166.12","gene_symbol":"TRMT61A","gene_name":"tRNA methyltransferase 61A [Source:HGNC Symbol;Acc:HGNC:23790]","synonyms":"hTRM61,Gcd14p,GCD14,FLJ40452,C14orf172","biotype":"protein_coding","ncbi_id":"115708","summary":null,"start":103529184,"end":103537073,"strand":1,"description":"tRNA methyltransferase 61A [Source:HGNC Symbol;Acc:HGNC:23790]"}, {"versioned_ensembl_gene_id":"ENSG00000274362.1","gene_symbol":"AC226740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131795990,"end":131802689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188981.10","gene_symbol":"MSANTD1","gene_name":"Myb/SANT DNA binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33741]","synonyms":"LOC345222,C4orf44","biotype":"protein_coding","ncbi_id":"345222","summary":null,"start":3244369,"end":3271738,"strand":1,"description":"Myb/SANT DNA binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33741]"}, {"versioned_ensembl_gene_id":"ENSG00000125952.18","gene_symbol":"MAX","gene_name":"MYC associated factor X [Source:HGNC Symbol;Acc:HGNC:6913]","synonyms":"bHLHd4,bHLHd8,bHLHd7,bHLHd6,bHLHd5","biotype":"protein_coding","ncbi_id":"4149","summary":"The protein encoded by this gene is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":65006174,"end":65102695,"strand":-1,"description":"MYC associated factor X [Source:HGNC Symbol;Acc:HGNC:6913]"}, {"versioned_ensembl_gene_id":"ENSG00000273828.1","gene_symbol":"AL133227.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46364551,"end":46390885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107593.16","gene_symbol":"PKD2L1","gene_name":"polycystin 2 like 1, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9011]","synonyms":"TRPP3,PKDL,PKD2L,PCL","biotype":"protein_coding","ncbi_id":"9033","summary":"This gene encodes a member of the polycystin protein family. The encoded protein contains multiple transmembrane domains, and cytoplasmic N- and C-termini. The protein may be an integral membrane protein involved in cell-cell/matrix interactions. This protein functions as a calcium-regulated nonselective cation channel. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":100288154,"end":100330486,"strand":-1,"description":"polycystin 2 like 1, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9011]"}, {"versioned_ensembl_gene_id":"ENSG00000110711.9","gene_symbol":"AIP","gene_name":"aryl hydrocarbon receptor interacting protein [Source:HGNC Symbol;Acc:HGNC:358]","synonyms":"XAP2,FKBP16,ARA9","biotype":"protein_coding","ncbi_id":"9049","summary":"The protein encoded by this gene is a receptor for aryl hydrocarbons and a ligand-activated transcription factor. The encoded protein is found in the cytoplasm as part of a multiprotein complex, but upon binding of ligand is transported to the nucleus. This protein can regulate the expression of many xenobiotic metabolizing enzymes. Also, the encoded protein can bind specifically to and inhibit the activity of hepatitis B virus. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":67483041,"end":67491103,"strand":1,"description":"aryl hydrocarbon receptor interacting protein [Source:HGNC Symbol;Acc:HGNC:358]"}, {"versioned_ensembl_gene_id":"ENSG00000270728.1","gene_symbol":"AL035413.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19297080,"end":19297903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225849.2","gene_symbol":"MKRN7P","gene_name":"makorin ring finger protein 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:7119]","synonyms":"ZNF127L5,MKRNP3","biotype":"transcribed_processed_pseudogene","ncbi_id":"7686","summary":null,"start":46463719,"end":46477232,"strand":-1,"description":"makorin ring finger protein 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:7119]"}, {"versioned_ensembl_gene_id":"ENSG00000215452.5","gene_symbol":"ZNF663P","gene_name":"zinc finger protein 663, pseudogene [Source:HGNC Symbol;Acc:HGNC:25342]","synonyms":"ZNF663,DKFZp547G0215","biotype":"transcribed_unitary_pseudogene","ncbi_id":"100130934","summary":null,"start":46414228,"end":46459276,"strand":-1,"description":"zinc finger protein 663, pseudogene [Source:HGNC Symbol;Acc:HGNC:25342]"}, {"versioned_ensembl_gene_id":"ENSG00000184302.6","gene_symbol":"SIX6","gene_name":"SIX homeobox 6 [Source:HGNC Symbol;Acc:HGNC:10892]","synonyms":"Six9,OPTX2","biotype":"protein_coding","ncbi_id":"4990","summary":"The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in eye development. Defects in this gene are a cause of isolated microphthalmia with cataract type 2 (MCOPCT2). [provided by RefSeq, Jul 2008]","start":60508951,"end":60512850,"strand":1,"description":"SIX homeobox 6 [Source:HGNC Symbol;Acc:HGNC:10892]"}, {"versioned_ensembl_gene_id":"ENSG00000272372.1","gene_symbol":"AC009102.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56351886,"end":56353524,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275397.2","gene_symbol":"DHRS11","gene_name":"dehydrogenase/reductase 11 [Source:HGNC Symbol;Acc:HGNC:28639]","synonyms":"MGC4172,SDR24C1","biotype":"protein_coding","ncbi_id":"79154","summary":null,"start":36592761,"end":36601768,"strand":1,"description":"dehydrogenase/reductase 11 [Source:HGNC Symbol;Acc:HGNC:28639]"}, {"versioned_ensembl_gene_id":"ENSG00000243977.1","gene_symbol":"AC125604.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179649494,"end":179650200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214329.7","gene_symbol":"SLC9B1P2","gene_name":"solute carrier family 9 member B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37493]","synonyms":"NHEDC1P2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"389000","summary":null,"start":91883076,"end":91931714,"strand":-1,"description":"solute carrier family 9 member B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37493]"}, {"versioned_ensembl_gene_id":"ENSG00000258427.3","gene_symbol":"RBM8B","gene_name":"RNA binding motif protein 8B pseudogene [Source:HGNC Symbol;Acc:HGNC:13426]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"112846","summary":null,"start":60397757,"end":60398281,"strand":1,"description":"RNA binding motif protein 8B pseudogene [Source:HGNC Symbol;Acc:HGNC:13426]"}, {"versioned_ensembl_gene_id":"ENSG00000258670.1","gene_symbol":"AL049874.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60515119,"end":60554916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258692.2","gene_symbol":"SALL4P7","gene_name":"spalt like transcription factor 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43900]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"390483","summary":null,"start":60493766,"end":60496885,"strand":-1,"description":"spalt like transcription factor 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43900]"}, {"versioned_ensembl_gene_id":"ENSG00000279314.1","gene_symbol":"AC002525.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31960325,"end":31961946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183307.3","gene_symbol":"TMEM121B","gene_name":"transmembrane protein 121B [Source:HGNC Symbol;Acc:HGNC:1844]","synonyms":"CECR6","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17116299,"end":17121367,"strand":-1,"description":"transmembrane protein 121B [Source:HGNC Symbol;Acc:HGNC:1844]"}, {"versioned_ensembl_gene_id":"ENSG00000227863.2","gene_symbol":"AC002383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89443974,"end":89494262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258764.1","gene_symbol":"AL049874.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":60544400,"end":60544654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253795.1","gene_symbol":"MTND1P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42104]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873174","summary":null,"start":103085651,"end":103086590,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42104]"}, {"versioned_ensembl_gene_id":"ENSG00000235822.1","gene_symbol":"LINC01073","gene_name":"long intergenic non-protein coding RNA 1073 [Source:HGNC Symbol;Acc:HGNC:49114]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107080623","summary":null,"start":31985685,"end":31990997,"strand":1,"description":"long intergenic non-protein coding RNA 1073 [Source:HGNC Symbol;Acc:HGNC:49114]"}, {"versioned_ensembl_gene_id":"ENSG00000226586.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"D6S203,HLA-CDA12,CDA12,HLA-59","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":30085046,"end":30088419,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000182010.10","gene_symbol":"RTKN2","gene_name":"rhotekin 2 [Source:HGNC Symbol;Acc:HGNC:19364]","synonyms":"PLEKHK1,FLJ39352,Em:AC024597.2,bA531F24.1","biotype":"protein_coding","ncbi_id":"219790","summary":null,"start":62183035,"end":62268707,"strand":-1,"description":"rhotekin 2 [Source:HGNC Symbol;Acc:HGNC:19364]"}, {"versioned_ensembl_gene_id":"ENSG00000132640.14","gene_symbol":"BTBD3","gene_name":"BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15854]","synonyms":"KIAA0952,dJ742J24.1","biotype":"protein_coding","ncbi_id":"22903","summary":null,"start":11890723,"end":11926609,"strand":1,"description":"BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15854]"}, {"versioned_ensembl_gene_id":"ENSG00000274837.1","gene_symbol":"AC009233.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19932130,"end":19932500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273203.1","gene_symbol":"AC006946.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17067821,"end":17070675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226481.3","gene_symbol":"ACTR3BP2","gene_name":"ACTR3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38677]","synonyms":"FKSG73,FKSG73","biotype":"processed_pseudogene","ncbi_id":"440888","summary":null,"start":91940668,"end":91942040,"strand":1,"description":"ACTR3B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38677]"}, {"versioned_ensembl_gene_id":"ENSG00000237997.1","gene_symbol":"RCC2P2","gene_name":"regulator of chromosome condensation 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38419]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421075","summary":null,"start":19986575,"end":19987852,"strand":-1,"description":"regulator of chromosome condensation 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38419]"}, {"versioned_ensembl_gene_id":"ENSG00000177663.13","gene_symbol":"IL17RA","gene_name":"interleukin 17 receptor A [Source:HGNC Symbol;Acc:HGNC:5985]","synonyms":"CDw217,CD217,IL17R,IL-17RA,hIL-17R","biotype":"protein_coding","ncbi_id":"23765","summary":"Interleukin 17A (IL17A) is a proinflammatory cytokine secreted by activated T-lymphocytes. It is a potent inducer of the maturation of CD34-positive hematopoietic precursors into neutrophils. The transmembrane protein encoded by this gene (interleukin 17A receptor; IL17RA) is a ubiquitous type I membrane glycoprotein that binds with low affinity to interleukin 17A. Interleukin 17A and its receptor play a pathogenic role in many inflammatory and autoimmune diseases such as rheumatoid arthritis. Like other cytokine receptors, this receptor likely has a multimeric structure. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2014]","start":17084954,"end":17115694,"strand":1,"description":"interleukin 17 receptor A [Source:HGNC Symbol;Acc:HGNC:5985]"}, {"versioned_ensembl_gene_id":"ENSG00000180745.4","gene_symbol":"CLRN3","gene_name":"clarin 3 [Source:HGNC Symbol;Acc:HGNC:20795]","synonyms":"USH3AL1,TMEM12,MGC32871","biotype":"protein_coding","ncbi_id":"119467","summary":null,"start":127877841,"end":127892947,"strand":-1,"description":"clarin 3 [Source:HGNC Symbol;Acc:HGNC:20795]"}, {"versioned_ensembl_gene_id":"ENSG00000224459.1","gene_symbol":"AL450998.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15740051,"end":15749896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255538.1","gene_symbol":"OR10V2P","gene_name":"olfactory receptor family 10 subfamily V member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15137]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81343","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59748811,"end":59749574,"strand":1,"description":"olfactory receptor family 10 subfamily V member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15137]"}, {"versioned_ensembl_gene_id":"ENSG00000255139.1","gene_symbol":"AP000442.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59616429,"end":59639861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261476.1","gene_symbol":"AC009163.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75458252,"end":75460017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251385.2","gene_symbol":"MTCYBP16","gene_name":"mitochondrially encoded cytochrome b pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075126","summary":null,"start":64607703,"end":64608831,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:51969]"}, {"versioned_ensembl_gene_id":"ENSG00000249893.1","gene_symbol":"MTND6P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39479]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478950","summary":null,"start":64608905,"end":64609424,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39479]"}, {"versioned_ensembl_gene_id":"ENSG00000153774.8","gene_symbol":"CFDP1","gene_name":"craniofacial development protein 1 [Source:HGNC Symbol;Acc:HGNC:1873]","synonyms":"Yeti,SWC5,p97,CP27,CENP-29,BCNT","biotype":"protein_coding","ncbi_id":"10428","summary":null,"start":75293698,"end":75433485,"strand":-1,"description":"craniofacial development protein 1 [Source:HGNC Symbol;Acc:HGNC:1873]"}, {"versioned_ensembl_gene_id":"ENSG00000233604.1","gene_symbol":"DHFRP2","gene_name":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729816","summary":null,"start":31409367,"end":31409913,"strand":-1,"description":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]"}, {"versioned_ensembl_gene_id":"ENSG00000132846.5","gene_symbol":"ZBED3","gene_name":"zinc finger BED-type containing 3 [Source:HGNC Symbol;Acc:HGNC:20711]","synonyms":"MGC15435","biotype":"protein_coding","ncbi_id":"84327","summary":"This gene belongs to a class of genes that arose through hAT DNA transposition and that encode regulatory proteins. This gene is upregulated in lung cancer tissues, where the encoded protein causes an accumulation of beta-catenin and enhanced lung cancer cell invasion. In addition, the encoded protein can be secreted and be involved in resistance to insulin. [provided by RefSeq, Jul 2016]","start":77072072,"end":77087323,"strand":-1,"description":"zinc finger BED-type containing 3 [Source:HGNC Symbol;Acc:HGNC:20711]"}, {"versioned_ensembl_gene_id":"ENSG00000196611.4","gene_symbol":"MMP1","gene_name":"matrix metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:7155]","synonyms":"CLG","biotype":"protein_coding","ncbi_id":"4312","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down the interstitial collagens, including types I, II, and III. The gene is part of a cluster of MMP genes on chromosome 11. Mutations in this gene are associated with chronic obstructive pulmonary disease (COPD). Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":102789920,"end":102798160,"strand":-1,"description":"matrix metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:7155]"}, {"versioned_ensembl_gene_id":"ENSG00000013563.13","gene_symbol":"DNASE1L1","gene_name":"deoxyribonuclease 1 like 1 [Source:HGNC Symbol;Acc:HGNC:2957]","synonyms":"XIB,DNL1L,DNASEX,DNAS1L1","biotype":"protein_coding","ncbi_id":"1774","summary":"This gene encodes a deoxyribonuclease protein that shows high sequence similarity to DNase I. The encoded protein is localized to the endoplasmic reticulum and modified by N-linked glycosylation. Alternate transcriptional splice variants encoding the same protein have been observed. [provided by RefSeq, Jan 2015]","start":154401238,"end":154412112,"strand":-1,"description":"deoxyribonuclease 1 like 1 [Source:HGNC Symbol;Acc:HGNC:2957]"}, {"versioned_ensembl_gene_id":"ENSG00000152475.6","gene_symbol":"ZNF837","gene_name":"zinc finger protein 837 [Source:HGNC Symbol;Acc:HGNC:25164]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116412","summary":null,"start":58367618,"end":58381060,"strand":-1,"description":"zinc finger protein 837 [Source:HGNC Symbol;Acc:HGNC:25164]"}, {"versioned_ensembl_gene_id":"ENSG00000253768.1","gene_symbol":"AC008663.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173562478,"end":173573199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143952.19","gene_symbol":"VPS54","gene_name":"VPS54, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:18652]","synonyms":"PPP1R164,HCC8","biotype":"protein_coding","ncbi_id":"51542","summary":"This gene encodes for a protein that in yeast forms part of a trimeric vacuolar-protein-sorting complex that is required for retrograde transport of proteins from prevacuoles to the late Golgi compartment. As in yeast, mammalian Vps54 proteins contain a coiled-coil region and dileucine motifs. Alternative splicing results in multiple transcript variants encoding different isoforms [provided by RefSeq, Jul 2008]","start":63892146,"end":64019072,"strand":-1,"description":"VPS54, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:18652]"}, {"versioned_ensembl_gene_id":"ENSG00000255057.1","gene_symbol":"AP003041.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130008586,"end":130009765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197588.9","gene_symbol":"KLKP1","gene_name":"kallikrein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21260]","synonyms":"YKLK1,PsiKLK1,KLK31P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"606293","summary":null,"start":50882096,"end":50896398,"strand":-1,"description":"kallikrein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21260]"}, {"versioned_ensembl_gene_id":"ENSG00000267026.5","gene_symbol":"AL136084.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98847172,"end":98872415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251211.1","gene_symbol":"AC136632.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178165702,"end":178166562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115594.11","gene_symbol":"IL1R1","gene_name":"interleukin 1 receptor type 1 [Source:HGNC Symbol;Acc:HGNC:5993]","synonyms":"IL1RA,IL1R,D2S1473,CD121A","biotype":"protein_coding","ncbi_id":"3554","summary":"This gene encodes a cytokine receptor that belongs to the interleukin-1 receptor family. The encoded protein is a receptor for interleukin-1 alpha, interleukin-1 beta, and interleukin-1 receptor antagonist. It is an important mediator involved in many cytokine-induced immune and inflammatory responses. This gene is located in a cluster of related cytokine receptor genes on chromosome 2q12. [provided by RefSeq, Dec 2013]","start":102064544,"end":102179874,"strand":1,"description":"interleukin 1 receptor type 1 [Source:HGNC Symbol;Acc:HGNC:5993]"}, {"versioned_ensembl_gene_id":"ENSG00000115935.17","gene_symbol":"WIPF1","gene_name":"WAS/WASL interacting protein family member 1 [Source:HGNC Symbol;Acc:HGNC:12736]","synonyms":"WASPIP,WIP","biotype":"protein_coding","ncbi_id":"7456","summary":"This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":174559572,"end":174682916,"strand":-1,"description":"WAS/WASL interacting protein family member 1 [Source:HGNC Symbol;Acc:HGNC:12736]"}, {"versioned_ensembl_gene_id":"ENSG00000139973.16","gene_symbol":"SYT16","gene_name":"synaptotagmin 16 [Source:HGNC Symbol;Acc:HGNC:23142]","synonyms":"Strep14,CHR14SYT,yt14r,SYT14L","biotype":"protein_coding","ncbi_id":"83851","summary":null,"start":61811974,"end":62112550,"strand":1,"description":"synaptotagmin 16 [Source:HGNC Symbol;Acc:HGNC:23142]"}, {"versioned_ensembl_gene_id":"ENSG00000233220.3","gene_symbol":"LINC00167","gene_name":"long intergenic non-protein coding RNA 167 [Source:HGNC Symbol;Acc:HGNC:30468]","synonyms":"NCRNA00167,FLJ31394,C11orf37","biotype":"lincRNA","ncbi_id":"440072","summary":null,"start":130002938,"end":130004356,"strand":1,"description":"long intergenic non-protein coding RNA 167 [Source:HGNC Symbol;Acc:HGNC:30468]"}, {"versioned_ensembl_gene_id":"ENSG00000229501.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31047850,"end":31053655,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000125430.8","gene_symbol":"HS3ST3B1","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 3B1 [Source:HGNC Symbol;Acc:HGNC:5198]","synonyms":"3OST3B1,30ST3B1","biotype":"protein_coding","ncbi_id":"9953","summary":"The protein encoded by this gene is a type II integral membrane protein that belongs to the 3-O-sulfotransferases family. These proteins catalyze the addition of sulfate groups at the 3-OH position of glucosamine in heparan sulfate. The substrate specificity of individual members of the family is based on prior modification of the heparan sulfate chain, thus allowing different members of the family to generate binding sites for different proteins on the same heparan sulfate chain. Following treatment with a histone deacetylase inhibitor, expression of this gene is activated in a pancreatic cell line. The increased expression results in promotion of the epithelial-mesenchymal transition. In addition, the modification catalyzed by this protein allows herpes simplex virus membrane fusion and penetration. A very closely related homolog with an almost identical sulfotransferase domain maps less than 1 Mb away. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":14301083,"end":14349404,"strand":1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 3B1 [Source:HGNC Symbol;Acc:HGNC:5198]"}, {"versioned_ensembl_gene_id":"ENSG00000251273.2","gene_symbol":"LINC02228","gene_name":"long intergenic non-protein coding RNA 2228 [Source:HGNC Symbol;Acc:HGNC:53097]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374694","summary":null,"start":25087450,"end":25191020,"strand":-1,"description":"long intergenic non-protein coding RNA 2228 [Source:HGNC Symbol;Acc:HGNC:53097]"}, {"versioned_ensembl_gene_id":"ENSG00000120509.10","gene_symbol":"PDZD11","gene_name":"PDZ domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28034]","synonyms":"PDZK11","biotype":"protein_coding","ncbi_id":"51248","summary":null,"start":70286595,"end":70290514,"strand":-1,"description":"PDZ domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28034]"}, {"versioned_ensembl_gene_id":"ENSG00000267373.1","gene_symbol":"AC008894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16103761,"end":16104254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250524.1","gene_symbol":"AC106821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24881943,"end":24885461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112339.14","gene_symbol":"HBS1L","gene_name":"HBS1 like translational GTPase [Source:HGNC Symbol;Acc:HGNC:4834]","synonyms":"KIAA1038,HSPC276,HBS1,ERFS,eRF3c,EF-1a,DKFZp434g247","biotype":"protein_coding","ncbi_id":"10767","summary":"This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":134960378,"end":135103056,"strand":-1,"description":"HBS1 like translational GTPase [Source:HGNC Symbol;Acc:HGNC:4834]"}, {"versioned_ensembl_gene_id":"ENSG00000196628.15","gene_symbol":"TCF4","gene_name":"transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:11634]","synonyms":"SEF2-1B,ITF2,E2-2,bHLHb19","biotype":"protein_coding","ncbi_id":"6925","summary":"This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016]","start":55222331,"end":55664787,"strand":-1,"description":"transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:11634]"}, {"versioned_ensembl_gene_id":"ENSG00000225802.3","gene_symbol":"WARSP1","gene_name":"tryptophanyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50482]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"341112","summary":null,"start":59255360,"end":59259486,"strand":1,"description":"tryptophanyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50482]"}, {"versioned_ensembl_gene_id":"ENSG00000185000.11","gene_symbol":"DGAT1","gene_name":"diacylglycerol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2843]","synonyms":"ARGP1,DGAT","biotype":"protein_coding","ncbi_id":"8694","summary":"This gene encodes an multipass transmembrane protein that functions as a key metabolic enzyme. The encoded protein catalyzes the conversion of diacylglycerol and fatty acyl CoA to triacylglycerol. This enzyme can also transfer acyl CoA to retinol. Activity of this protein may be associated with obesity and other metabolic diseases. [provided by RefSeq, Jul 2013]","start":144314584,"end":144326910,"strand":-1,"description":"diacylglycerol O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:2843]"}, {"versioned_ensembl_gene_id":"ENSG00000256185.1","gene_symbol":"AC055720.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":26335864,"end":26336950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276173.2","gene_symbol":"IGHA2","gene_name":"immunoglobulin heavy constant alpha 2 (A2m marker) [Source:HGNC Symbol;Acc:HGNC:5479]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3494","summary":null,"start":105588247,"end":105589753,"strand":-1,"description":"immunoglobulin heavy constant alpha 2 (A2m marker) [Source:HGNC Symbol;Acc:HGNC:5479]"}, {"versioned_ensembl_gene_id":"ENSG00000250848.1","gene_symbol":"AC021087.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":288833,"end":290321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167286.9","gene_symbol":"CD3D","gene_name":"CD3d molecule [Source:HGNC Symbol;Acc:HGNC:1673]","synonyms":"T3D","biotype":"protein_coding","ncbi_id":"915","summary":"The protein encoded by this gene is part of the T-cell receptor/CD3 complex (TCR/CD3 complex) and is involved in T-cell development and signal transduction. The encoded membrane protein represents the delta subunit of the CD3 complex, and along with four other CD3 subunits, binds either TCR alpha/beta or TCR gamma/delta to form the TCR/CD3 complex on the surface of T-cells. Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK). Two transcript variants encoding different isoforms have been found for this gene. Other variants may also exist, but the full-length natures of their transcripts has yet to be defined. [provided by RefSeq, Feb 2009]","start":118338954,"end":118342744,"strand":-1,"description":"CD3d molecule [Source:HGNC Symbol;Acc:HGNC:1673]"}, {"versioned_ensembl_gene_id":"ENSG00000255151.2","gene_symbol":"GLYATL1P3","gene_name":"glycine-N-acyltransferase like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37865]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287520","summary":null,"start":59086307,"end":59094786,"strand":1,"description":"glycine-N-acyltransferase like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37865]"}, {"versioned_ensembl_gene_id":"ENSG00000273212.1","gene_symbol":"AC000068.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19456503,"end":19456962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188677.14","gene_symbol":"PARVB","gene_name":"parvin beta [Source:HGNC Symbol;Acc:HGNC:14653]","synonyms":"CGI-56","biotype":"protein_coding","ncbi_id":"29780","summary":"This gene encodes a member of the parvin family of actin-binding proteins, which play a role in cytoskeleton organization and cell adhesion. These proteins are associated with focal contacts and contain calponin homology domains that bind to actin filaments. This family member binds to alphaPIX and alpha-actinin, and it can inhibit the activity of integrin-linked kinase. This protein also functions in tumor suppression. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":43999211,"end":44172949,"strand":1,"description":"parvin beta [Source:HGNC Symbol;Acc:HGNC:14653]"}, {"versioned_ensembl_gene_id":"ENSG00000215022.7","gene_symbol":"AL008729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13264861,"end":13295586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261720.1","gene_symbol":"AC009041.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1065240,"end":1066502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233526.1","gene_symbol":"RFC5P1","gene_name":"replication factor C 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50450]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421549","summary":null,"start":77072100,"end":77073295,"strand":1,"description":"replication factor C 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50450]"}, {"versioned_ensembl_gene_id":"ENSG00000229155.1","gene_symbol":"LINC02038","gene_name":"long intergenic non-protein coding RNA 2038 [Source:HGNC Symbol;Acc:HGNC:52878]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374285","summary":null,"start":193842560,"end":193844024,"strand":-1,"description":"long intergenic non-protein coding RNA 2038 [Source:HGNC Symbol;Acc:HGNC:52878]"}, {"versioned_ensembl_gene_id":"ENSG00000175155.8","gene_symbol":"YPEL2","gene_name":"yippee like 2 [Source:HGNC Symbol;Acc:HGNC:18326]","synonyms":"FKSG4","biotype":"protein_coding","ncbi_id":"388403","summary":null,"start":59331689,"end":59401729,"strand":1,"description":"yippee like 2 [Source:HGNC Symbol;Acc:HGNC:18326]"}, {"versioned_ensembl_gene_id":"ENSG00000231159.1","gene_symbol":"OFD1P8Y","gene_name":"OFD1 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:23880]","synonyms":"OFDYP8,OFD1PY8,OFD1P8","biotype":"unprocessed_pseudogene","ncbi_id":"386692","summary":null,"start":21972313,"end":22005349,"strand":1,"description":"OFD1 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:23880]"}, {"versioned_ensembl_gene_id":"ENSG00000273098.1","gene_symbol":"AC005303.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13095908,"end":13100928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218208.1","gene_symbol":"RPS27AP11","gene_name":"ribosomal protein S27a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36126]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728590","summary":null,"start":113581501,"end":113581947,"strand":1,"description":"ribosomal protein S27a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36126]"}, {"versioned_ensembl_gene_id":"ENSG00000116641.17","gene_symbol":"DOCK7","gene_name":"dedicator of cytokinesis 7 [Source:HGNC Symbol;Acc:HGNC:19190]","synonyms":"ZIR2,KIAA1771","biotype":"protein_coding","ncbi_id":"85440","summary":"The protein encoded by this gene is a guanine nucleotide exchange factor (GEF) that plays a role in axon formation and neuronal polarization. The encoded protein displays GEF activity toward RAC1 and RAC3 Rho small GTPases but not toward CDC42. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":62454298,"end":62688368,"strand":-1,"description":"dedicator of cytokinesis 7 [Source:HGNC Symbol;Acc:HGNC:19190]"}, {"versioned_ensembl_gene_id":"ENSG00000131016.16","gene_symbol":"AKAP12","gene_name":"A-kinase anchoring protein 12 [Source:HGNC Symbol;Acc:HGNC:370]","synonyms":"SSeCKS,AKAP250","biotype":"protein_coding","ncbi_id":"9590","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is expressed in endothelial cells, cultured fibroblasts, and osteosarcoma cells. It associates with protein kinases A and C and phosphatase, and serves as a scaffold protein in signal transduction. This protein and RII PKA colocalize at the cell periphery. This protein is a cell growth-related protein. Antibodies to this protein can be produced by patients with myasthenia gravis. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":151239999,"end":151358557,"strand":1,"description":"A-kinase anchoring protein 12 [Source:HGNC Symbol;Acc:HGNC:370]"}, {"versioned_ensembl_gene_id":"ENSG00000267741.1","gene_symbol":"UBE2L4","gene_name":"ubiquitin conjugating enzyme E2 L4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"7333","summary":null,"start":9774497,"end":9774960,"strand":1,"description":"ubiquitin conjugating enzyme E2 L4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12489]"}, {"versioned_ensembl_gene_id":"ENSG00000227444.1","gene_symbol":"AC007322.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21918935,"end":21921106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236132.1","gene_symbol":"AL022331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31816379,"end":31817491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279111.2","gene_symbol":"OR10X1","gene_name":"olfactory receptor family 10 subfamily X member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14995]","synonyms":"OR10X1P","biotype":"polymorphic_pseudogene","ncbi_id":"128367","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":158578919,"end":158579899,"strand":-1,"description":"olfactory receptor family 10 subfamily X member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14995]"}, {"versioned_ensembl_gene_id":"ENSG00000272047.1","gene_symbol":"GTF2H5","gene_name":"general transcription factor IIH subunit 5 [Source:HGNC Symbol;Acc:HGNC:21157]","synonyms":"TTD,TFIIH,TFB5,FLJ30544,C6orf175,bA120J8.2,TTDA,TTD-A","biotype":"protein_coding","ncbi_id":"404672","summary":"This gene encodes a subunit of transcription/repair factor TFIIH, which functions in gene transcription and DNA repair. This protein stimulates ERCC3/XPB ATPase activity to trigger DNA opening during DNA repair, and is implicated in regulating cellular levels of TFIIH. Mutations in this gene result in trichothiodystrophy, complementation group A. [provided by RefSeq, Mar 2009]","start":158168352,"end":158199344,"strand":1,"description":"general transcription factor IIH subunit 5 [Source:HGNC Symbol;Acc:HGNC:21157]"}, {"versioned_ensembl_gene_id":"ENSG00000172250.14","gene_symbol":"SERHL","gene_name":"serine hydrolase-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:14408]","synonyms":"HS126B42,dJ222E13.1,BK126B4.1","biotype":"processed_transcript","ncbi_id":"94009","summary":null,"start":42500579,"end":42512560,"strand":1,"description":"serine hydrolase-like (pseudogene) [Source:HGNC Symbol;Acc:HGNC:14408]"}, {"versioned_ensembl_gene_id":"ENSG00000270837.1","gene_symbol":"HNRNPDLP4","gene_name":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48808]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421657","summary":null,"start":58049046,"end":58049346,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48808]"}, {"versioned_ensembl_gene_id":"ENSG00000268660.1","gene_symbol":"LETM1P2","gene_name":"leucine zipper and EF-hand containing transmembrane protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33985]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131934","summary":null,"start":58044592,"end":58046769,"strand":1,"description":"leucine zipper and EF-hand containing transmembrane protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33985]"}, {"versioned_ensembl_gene_id":"ENSG00000226867.1","gene_symbol":"AC244505.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52781452,"end":52785786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205364.3","gene_symbol":"MT1M","gene_name":"metallothionein 1M [Source:HGNC Symbol;Acc:HGNC:14296]","synonyms":"MT1K,MT1","biotype":"protein_coding","ncbi_id":"4499","summary":"This gene encodes a member of the metallothionein superfamily, type 1 family. Metallothioneins have a high content of cysteine residues that bind various heavy metals. These genes are transcriptionally regulated by both heavy metals and glucocorticoids. [provided by RefSeq, Oct 2011]","start":56632233,"end":56633986,"strand":1,"description":"metallothionein 1M [Source:HGNC Symbol;Acc:HGNC:14296]"}, {"versioned_ensembl_gene_id":"ENSG00000182698.11","gene_symbol":"RESP18","gene_name":"regulated endocrine specific protein 18 [Source:HGNC Symbol;Acc:HGNC:33762]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389075","summary":null,"start":219327409,"end":219333177,"strand":-1,"description":"regulated endocrine specific protein 18 [Source:HGNC Symbol;Acc:HGNC:33762]"}, {"versioned_ensembl_gene_id":"ENSG00000230307.1","gene_symbol":"OR6C5P","gene_name":"olfactory receptor family 6 subfamily C member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31292]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390320","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55311835,"end":55312757,"strand":1,"description":"olfactory receptor family 6 subfamily C member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:31292]"}, {"versioned_ensembl_gene_id":"ENSG00000197706.3","gene_symbol":"OR6C74","gene_name":"olfactory receptor family 6 subfamily C member 74 [Source:HGNC Symbol;Acc:HGNC:31303]","synonyms":null,"biotype":"protein_coding","ncbi_id":"254783","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55247198,"end":55248302,"strand":1,"description":"olfactory receptor family 6 subfamily C member 74 [Source:HGNC Symbol;Acc:HGNC:31303]"}, {"versioned_ensembl_gene_id":"ENSG00000106772.17","gene_symbol":"PRUNE2","gene_name":"prune homolog 2 [Source:HGNC Symbol;Acc:HGNC:25209]","synonyms":"KIAA0367,C9orf65,BNIPXL,BMCC1,bA214N16.3,A214N16.3","biotype":"protein_coding","ncbi_id":"158471","summary":"The protein encoded by this gene belongs to the B-cell CLL/lymphoma 2 and adenovirus E1B 19 kDa interacting family, whose members play roles in many cellular processes including apotosis, cell transformation, and synaptic function. Several functions for this protein have been demonstrated including suppression of Ras homolog family member A activity, which results in reduced stress fiber formation and suppression of oncogenic cellular transformation. A high molecular weight isoform of this protein has also been shown to colocalize with Adaptor protein complex 2, beta-Adaptin and endodermal markers, suggesting an involvement in post-endocytic trafficking. In prostate cancer cells, this gene acts as a tumor suppressor and its expression is regulated by prostate cancer antigen 3, a non-protein coding gene on the opposite DNA strand in an intron of this gene. Prostate cancer antigen 3 regulates levels of this gene through formation of a double-stranded RNA that undergoes adenosine deaminase actin on RNA-dependent adenosine-to-inosine RNA editing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":76611376,"end":76906087,"strand":-1,"description":"prune homolog 2 [Source:HGNC Symbol;Acc:HGNC:25209]"}, {"versioned_ensembl_gene_id":"ENSG00000282953.1","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195739964,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000268375.1","gene_symbol":"AC010325.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50792685,"end":50793584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260796.1","gene_symbol":"AC145285.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28820570,"end":28822033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171150.7","gene_symbol":"SOCS5","gene_name":"suppressor of cytokine signaling 5 [Source:HGNC Symbol;Acc:HGNC:16852]","synonyms":"SOCS-5,KIAA0671,CISH6,Cish5,CIS6","biotype":"protein_coding","ncbi_id":"9655","summary":"The protein encoded by this gene contains a SH2 domain and a SOCS BOX domain. The protein thus belongs to the suppressor of cytokine signaling (SOCS) family, also known as STAT-induced STAT inhibitor (SSI) protein family. SOCS family members are known to be cytokine-inducible negative regulators of cytokine signaling. The specific function of this protein has not yet been determined. Two alternatively spliced transcript variants encoding an identical protein have been reported. [provided by RefSeq, Jul 2008]","start":46698952,"end":46763129,"strand":1,"description":"suppressor of cytokine signaling 5 [Source:HGNC Symbol;Acc:HGNC:16852]"}, {"versioned_ensembl_gene_id":"ENSG00000253645.1","gene_symbol":"AC108863.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38970360,"end":38973011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234865.3","gene_symbol":"AC026784.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":23980587,"end":23980938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196475.5","gene_symbol":"GK2","gene_name":"glycerol kinase 2 [Source:HGNC Symbol;Acc:HGNC:4291]","synonyms":"GKTA,GKP2","biotype":"protein_coding","ncbi_id":"2712","summary":null,"start":79406352,"end":79408293,"strand":-1,"description":"glycerol kinase 2 [Source:HGNC Symbol;Acc:HGNC:4291]"}, {"versioned_ensembl_gene_id":"ENSG00000255113.1","gene_symbol":"OR4A48P","gene_name":"olfactory receptor family 4 subfamily A member 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:31267]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403254","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48492026,"end":48492416,"strand":1,"description":"olfactory receptor family 4 subfamily A member 48 pseudogene [Source:HGNC Symbol;Acc:HGNC:31267]"}, {"versioned_ensembl_gene_id":"ENSG00000182853.11","gene_symbol":"VMO1","gene_name":"vitelline membrane outer layer 1 homolog [Source:HGNC Symbol;Acc:HGNC:30387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284013","summary":null,"start":4785285,"end":4786433,"strand":-1,"description":"vitelline membrane outer layer 1 homolog [Source:HGNC Symbol;Acc:HGNC:30387]"}, {"versioned_ensembl_gene_id":"ENSG00000259699.2","gene_symbol":"HMGB1P8","gene_name":"high mobility group box 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:13319]","synonyms":"HMGB1L8,HMG1L8","biotype":"processed_pseudogene","ncbi_id":"692147","summary":null,"start":89135547,"end":89136495,"strand":-1,"description":"high mobility group box 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:13319]"}, {"versioned_ensembl_gene_id":"ENSG00000228771.1","gene_symbol":"BX510359.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52583989,"end":52586312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231593.1","gene_symbol":"BX510359.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52561769,"end":52562301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229040.2","gene_symbol":"CR774181.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29137903,"end":29138839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227058.1","gene_symbol":"BX510359.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52545151,"end":52547695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023697.12","gene_symbol":"DERA","gene_name":"deoxyribose-phosphate aldolase [Source:HGNC Symbol;Acc:HGNC:24269]","synonyms":"DEOC,CGI-26","biotype":"protein_coding","ncbi_id":"51071","summary":null,"start":15911172,"end":16037282,"strand":1,"description":"deoxyribose-phosphate aldolase [Source:HGNC Symbol;Acc:HGNC:24269]"}, {"versioned_ensembl_gene_id":"ENSG00000196642.18","gene_symbol":"RABL6","gene_name":"RAB, member RAS oncogene family like 6 [Source:HGNC Symbol;Acc:HGNC:24703]","synonyms":"C9orf86,bA216L13.9,RBEL1,pp8875,Parf,FLJ13045,FLJ10101","biotype":"protein_coding","ncbi_id":"55684","summary":"This gene encodes a member of the Ras superfamily of small GTPases. The encoded protein binds to both GTP and GDP and may play a role in cell growth and survival. Overexpression of this gene may play a role in breast cancer tumorigenesis, and pseudogenes of this gene are located on the long arm of chromosome 2 and the short arm of chromosome 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":136807943,"end":136841187,"strand":1,"description":"RAB, member RAS oncogene family like 6 [Source:HGNC Symbol;Acc:HGNC:24703]"}, {"versioned_ensembl_gene_id":"ENSG00000265443.1","gene_symbol":"AC127024.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30726305,"end":30727564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087111.20","gene_symbol":"PIGS","gene_name":"phosphatidylinositol glycan anchor biosynthesis class S [Source:HGNC Symbol;Acc:HGNC:14937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94005","summary":"This gene encodes a protein that is involved in GPI-anchor biosynthesis. The glycosylphosphatidylinositol (GPI) anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This gene encodes an essential component of the multisubunit enzyme, GPI transamidase. GPI transamidase mediates GPI anchoring in the endoplasmic reticulum, by catalyzing the transfer of fully assembled GPI units to proteins. [provided by RefSeq, Jul 2008]","start":28553383,"end":28571872,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class S [Source:HGNC Symbol;Acc:HGNC:14937]"}, {"versioned_ensembl_gene_id":"ENSG00000277149.4","gene_symbol":"TYW1B","gene_name":"tRNA-yW synthesizing protein 1 homolog B [Source:HGNC Symbol;Acc:HGNC:33908]","synonyms":"RSAFD2,NCRNA00069,MGC87315,LINC00069","biotype":"protein_coding","ncbi_id":"441250","summary":"Wybutosine is a hypermodified guanosine found in phenylalanine tRNA. Wybutosine functions to stabilize codon-anticodon interactions during ribosome decoding and therefore supports the maintenance of the reading frame. In yeast, the homolog of this gene is essential for the synthesis of wybutosine. The human genome contains two closely related genes that putatively function in wybutosine synthesis. The open reading frame of this locus is disrupted in some individuals. Thus, this locus appears to be an evolving pseudogene, but may still be functional in some members of the population. [provided by RefSeq, Apr 2014]","start":72558744,"end":72828198,"strand":-1,"description":"tRNA-yW synthesizing protein 1 homolog B [Source:HGNC Symbol;Acc:HGNC:33908]"}, {"versioned_ensembl_gene_id":"ENSG00000111886.10","gene_symbol":"GABRR2","gene_name":"gamma-aminobutyric acid type A receptor rho2 subunit [Source:HGNC Symbol;Acc:HGNC:4091]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2570","summary":"Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA receptors, which are ligand-gated chloride channels. The protein encoded by this gene is a member of the rho subunit family and is a component of the GABA type A receptor complex. This gene exists on chromosome 6q next to the gene encoding the rho 1 subunit of the GABA type A receptor, in a region thought to be associated with susceptibility for psychiatric disorders and epilepsy. Polymorphisms in this gene may also be associated with alcohol dependence, and general cognitive ability. [provided by RefSeq, Apr 2016]","start":89257208,"end":89315299,"strand":-1,"description":"gamma-aminobutyric acid type A receptor rho2 subunit [Source:HGNC Symbol;Acc:HGNC:4091]"}, {"versioned_ensembl_gene_id":"ENSG00000225417.1","gene_symbol":"AL049648.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20214299,"end":20215262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270694.1","gene_symbol":"AC211469.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72722885,"end":72723089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109103.11","gene_symbol":"UNC119","gene_name":"unc-119 lipid binding chaperone [Source:HGNC Symbol;Acc:HGNC:12565]","synonyms":"POC7A,POC7,HRG4","biotype":"protein_coding","ncbi_id":"9094","summary":"This gene is specifically expressed in the photoreceptors in the retina. The encoded product shares strong homology with the C. elegans unc119 protein and it can functionally complement the C. elegans unc119 mutation. It has been localized to the photoreceptor synapses in the outer plexiform layer of the retina, and suggested to play a role in the mechanism of photoreceptor neurotransmitter release through the synaptic vesicle cycle. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":28546707,"end":28552668,"strand":-1,"description":"unc-119 lipid binding chaperone [Source:HGNC Symbol;Acc:HGNC:12565]"}, {"versioned_ensembl_gene_id":"ENSG00000204366.3","gene_symbol":"ZBTB12","gene_name":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]","synonyms":"C6orf46,NG35,G10,D6S59E","biotype":"protein_coding","ncbi_id":"221527","summary":null,"start":31899607,"end":31901992,"strand":-1,"description":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]"}, {"versioned_ensembl_gene_id":"ENSG00000259350.2","gene_symbol":"AC067805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88952683,"end":88953460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234616.8","gene_symbol":"JRK","gene_name":"Jrk helix-turn-helix protein [Source:HGNC Symbol;Acc:HGNC:6199]","synonyms":"JH8,jerky","biotype":"protein_coding","ncbi_id":"8629","summary":"This gene encodes a conserved protein that is similar to DNA-binding proteins, such as major centromere autoantigen B (CENPB). Inactivation of the related gene in mice resulted in epileptic seizures. Childhood Absence Epilepsy (CAE) has been mapped to the same chromosomal location (8q24.3) as this gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":142657460,"end":142681968,"strand":-1,"description":"Jrk helix-turn-helix protein [Source:HGNC Symbol;Acc:HGNC:6199]"}, {"versioned_ensembl_gene_id":"ENSG00000281718.1","gene_symbol":"GRAMD4P6","gene_name":"GRAM domain containing 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631250","summary":null,"start":21383905,"end":21384148,"strand":1,"description":"GRAM domain containing 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49141]"}, {"versioned_ensembl_gene_id":"ENSG00000156531.16","gene_symbol":"PHF6","gene_name":"PHD finger protein 6 [Source:HGNC Symbol;Acc:HGNC:18145]","synonyms":"MGC14797,KIAA1823,CENP-31,BORJ,BFLS","biotype":"protein_coding","ncbi_id":"84295","summary":"This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010]","start":134373253,"end":134428791,"strand":1,"description":"PHD finger protein 6 [Source:HGNC Symbol;Acc:HGNC:18145]"}, {"versioned_ensembl_gene_id":"ENSG00000177025.3","gene_symbol":"C19orf18","gene_name":"chromosome 19 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:28642]","synonyms":"MGC41906","biotype":"protein_coding","ncbi_id":"147685","summary":null,"start":57958437,"end":57974534,"strand":-1,"description":"chromosome 19 open reading frame 18 [Source:HGNC Symbol;Acc:HGNC:28642]"}, {"versioned_ensembl_gene_id":"ENSG00000169220.17","gene_symbol":"RGS14","gene_name":"regulator of G protein signaling 14 [Source:HGNC Symbol;Acc:HGNC:9996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10636","summary":"This gene encodes a member of the regulator of G-protein signaling family. This protein contains one RGS domain, two Raf-like Ras-binding domains (RBDs), and one GoLoco domain. The protein attenuates the signaling activity of G-proteins by binding, through its GoLoco domain, to specific types of activated, GTP-bound G alpha subunits. Acting as a GTPase activating protein (GAP), the protein increases the rate of conversion of the GTP to GDP. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":177357837,"end":177372601,"strand":1,"description":"regulator of G protein signaling 14 [Source:HGNC Symbol;Acc:HGNC:9996]"}, {"versioned_ensembl_gene_id":"ENSG00000213625.8","gene_symbol":"LEPROT","gene_name":"leptin receptor overlapping transcript [Source:HGNC Symbol;Acc:HGNC:29477]","synonyms":"OBRGRP,OB-RGRP,FLJ90360,VPS55","biotype":"protein_coding","ncbi_id":"54741","summary":"LEPROT is associated with the Golgi complex and endosomes and has a role in cell surface expression of growth hormone receptor (GHR; MIM 600946) and leptin receptor (OBR, or LEPR; MIM 601007), thereby altering receptor-mediated cell signaling (Couturier et al., 2007 [PubMed 18042720]; Touvier et al., 2009 [PubMed 19907080]).[supplied by OMIM, Jul 2010]","start":65420587,"end":65436007,"strand":1,"description":"leptin receptor overlapping transcript [Source:HGNC Symbol;Acc:HGNC:29477]"}, {"versioned_ensembl_gene_id":"ENSG00000231202.1","gene_symbol":"TRGVB","gene_name":"T-cell receptor gamma variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12297]","synonyms":"V6P,TCRGVB","biotype":"TR_V_pseudogene","ncbi_id":"6987","summary":null,"start":38295763,"end":38296233,"strand":-1,"description":"T-cell receptor gamma variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12297]"}, {"versioned_ensembl_gene_id":"ENSG00000188408.5","gene_symbol":"MAGEB5","gene_name":"MAGE family member B5 [Source:HGNC Symbol;Acc:HGNC:23795]","synonyms":"MAGE-B5,CT3.3","biotype":"protein_coding","ncbi_id":"347541","summary":null,"start":26216169,"end":26218270,"strand":1,"description":"MAGE family member B5 [Source:HGNC Symbol;Acc:HGNC:23795]"}, {"versioned_ensembl_gene_id":"ENSG00000234495.7","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RNF76,RFP","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28902993,"end":28923981,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000261976.2","gene_symbol":"AC091062.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50840057,"end":50841626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253110.1","gene_symbol":"AC011410.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":171773652,"end":171774739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081721.11","gene_symbol":"DUSP12","gene_name":"dual specificity phosphatase 12 [Source:HGNC Symbol;Acc:HGNC:3067]","synonyms":"YVH1,DUSP1","biotype":"protein_coding","ncbi_id":"11266","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product is the human ortholog of the Saccharomyces cerevisiae YVH1 protein tyrosine phosphatase. It is localized predominantly in the nucleus, and is novel in that it contains, and is regulated by a zinc finger domain. [provided by RefSeq, Jul 2008]","start":161749758,"end":161757238,"strand":1,"description":"dual specificity phosphatase 12 [Source:HGNC Symbol;Acc:HGNC:3067]"}, {"versioned_ensembl_gene_id":"ENSG00000131019.10","gene_symbol":"ULBP3","gene_name":"UL16 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:14895]","synonyms":"RAET1N","biotype":"protein_coding","ncbi_id":"79465","summary":"The protein encoded by this gene is one of several related ligands of the KLRK1/NKG2D receptor, which is found in primary NK cells. Binding of these ligands to the receptor activates several signal transduction pathways, including the JAK2, STAT5, and ERK pathways. The encoded protein is expressed solubly and on the surface of many tumor cells, making it potentially an important target for therapeutics. [provided by RefSeq, Nov 2015]","start":150063150,"end":150069095,"strand":-1,"description":"UL16 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:14895]"}, {"versioned_ensembl_gene_id":"ENSG00000257528.1","gene_symbol":"KRT8P19","gene_name":"keratin 8 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644998","summary":null,"start":61879318,"end":61880772,"strand":1,"description":"keratin 8 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33371]"}, {"versioned_ensembl_gene_id":"ENSG00000231052.1","gene_symbol":"AL353614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2541097,"end":2541635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270279.1","gene_symbol":"AL132655.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58754351,"end":58756838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149328.14","gene_symbol":"GLB1L2","gene_name":"galactosidase beta 1 like 2 [Source:HGNC Symbol;Acc:HGNC:25129]","synonyms":null,"biotype":"protein_coding","ncbi_id":"89944","summary":null,"start":134331874,"end":134378341,"strand":1,"description":"galactosidase beta 1 like 2 [Source:HGNC Symbol;Acc:HGNC:25129]"}, {"versioned_ensembl_gene_id":"ENSG00000178750.2","gene_symbol":"STX19","gene_name":"syntaxin 19 [Source:HGNC Symbol;Acc:HGNC:19300]","synonyms":"MGC21382","biotype":"protein_coding","ncbi_id":"415117","summary":null,"start":94014369,"end":94028610,"strand":-1,"description":"syntaxin 19 [Source:HGNC Symbol;Acc:HGNC:19300]"}, {"versioned_ensembl_gene_id":"ENSG00000230986.1","gene_symbol":"DDX3P2","gene_name":"DEAD-box helicase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42172]","synonyms":"DDX3YP2","biotype":"processed_pseudogene","ncbi_id":"100874489","summary":null,"start":74133004,"end":74133114,"strand":-1,"description":"DEAD-box helicase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42172]"}, {"versioned_ensembl_gene_id":"ENSG00000214049.6","gene_symbol":"UCA1","gene_name":"urothelial cancer associated 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37126]","synonyms":"UCAT1,onco-lncRNA-36,LINC00178,CUDR","biotype":"processed_transcript","ncbi_id":"652995","summary":"This gene produces a long non-coding RNA that was found to be upregulated in bladder cancer and plays a regulatory role in cell proliferation. This transcript regulates several genes, including CREB (cAMP responsive element binding protein). Expression of this transcript is regulated by CCAAT/enhancer-binding protein-alpha. [provided by RefSeq, Dec 2017]","start":15828961,"end":15836320,"strand":1,"description":"urothelial cancer associated 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37126]"}, {"versioned_ensembl_gene_id":"ENSG00000150676.12","gene_symbol":"CCDC83","gene_name":"coiled-coil domain containing 83 [Source:HGNC Symbol;Acc:HGNC:28535]","synonyms":"MGC34732,FLJ42119,CT148","biotype":"protein_coding","ncbi_id":"220047","summary":null,"start":85855101,"end":85920021,"strand":1,"description":"coiled-coil domain containing 83 [Source:HGNC Symbol;Acc:HGNC:28535]"}, {"versioned_ensembl_gene_id":"ENSG00000124839.12","gene_symbol":"RAB17","gene_name":"RAB17, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16523]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64284","summary":"The Rab subfamily of small GTPases plays an important role in the regulation of membrane trafficking. RAB17 is an epithelial cell-specific GTPase (Lutcke et al., 1993 [PubMed 8486736]).[supplied by OMIM, Oct 2009]","start":237574322,"end":237601614,"strand":-1,"description":"RAB17, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:16523]"}, {"versioned_ensembl_gene_id":"ENSG00000255933.1","gene_symbol":"AC117500.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131756966,"end":131758047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235719.3","gene_symbol":"FAM197Y10","gene_name":"family with sequence similarity 197 Y-linked member 10 [Source:HGNC Symbol;Acc:HGNC:37627]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288465","summary":null,"start":21465384,"end":21467163,"strand":-1,"description":"family with sequence similarity 197 Y-linked member 10 [Source:HGNC Symbol;Acc:HGNC:37627]"}, {"versioned_ensembl_gene_id":"ENSG00000279742.1","gene_symbol":"AP000974.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85852557,"end":85854943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234432.4","gene_symbol":"AC092171.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5426277,"end":5428927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163291.14","gene_symbol":"PAQR3","gene_name":"progestin and adipoQ receptor family member 3 [Source:HGNC Symbol;Acc:HGNC:30130]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152559","summary":"This gene encodes a seven-transmembrane protein localized in the Golgi apparatus in mammalian cells. The encoded protein belongs to the progestin and adipoQ receptor (PAQR) family. This protein functions as a tumor suppressor by inhibiting the Raf/MEK/ERK signaling cascade. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]","start":78887127,"end":78939438,"strand":-1,"description":"progestin and adipoQ receptor family member 3 [Source:HGNC Symbol;Acc:HGNC:30130]"}, {"versioned_ensembl_gene_id":"ENSG00000231240.1","gene_symbol":"KLF2P1","gene_name":"Kruppel like factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480253","summary":null,"start":130036958,"end":130038422,"strand":1,"description":"Kruppel like factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49280]"}, {"versioned_ensembl_gene_id":"ENSG00000171649.11","gene_symbol":"ZIK1","gene_name":"zinc finger protein interacting with K protein 1 [Source:HGNC Symbol;Acc:HGNC:33104]","synonyms":"ZNF762","biotype":"protein_coding","ncbi_id":"284307","summary":null,"start":57578456,"end":57593777,"strand":1,"description":"zinc finger protein interacting with K protein 1 [Source:HGNC Symbol;Acc:HGNC:33104]"}, {"versioned_ensembl_gene_id":"ENSG00000198791.11","gene_symbol":"CNOT7","gene_name":"CCR4-NOT transcription complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:14101]","synonyms":"CAF1","biotype":"protein_coding","ncbi_id":"29883","summary":"The protein encoded by this gene binds to an anti-proliferative protein, B-cell translocation protein 1, which negatively regulates cell proliferation. Binding of the two proteins, which is driven by phosphorylation of the anti-proliferative protein, causes signaling events in cell division that lead to changes in cell proliferation associated with cell-cell contact. The encoded protein downregulates the innate immune response and therefore provides a therapeutic target for enhancing its antimicrobial activity against foreign agents. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and X. [provided by RefSeq, Apr 2016]","start":17224964,"end":17246878,"strand":-1,"description":"CCR4-NOT transcription complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:14101]"}, {"versioned_ensembl_gene_id":"ENSG00000274569.1","gene_symbol":"AC024884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56413647,"end":56414045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117791.15","gene_symbol":"MARC2","gene_name":"mitochondrial amidoxime reducing component 2 [Source:HGNC Symbol;Acc:HGNC:26064]","synonyms":"MOSC2,FLJ20605","biotype":"protein_coding","ncbi_id":"54996","summary":"The protein encoded by this gene is an enzyme found in the outer mitochondrial membrane that reduces N-hydroxylated substrates. The encoded protein uses molybdenum as a cofactor and cytochrome b5 type B and NADH cytochrome b5 reductase as accessory proteins. One type of substrate used is N-hydroxylated nucleotide base analogues, which can be toxic to a cell. Other substrates include N(omega)-hydroxy-L-arginine (NOHA) and amidoxime prodrugs, which are activated by the encoded enzyme. Multiple transcript variants encoding the different isoforms have been found for this gene. [provided by RefSeq, Sep 2016]","start":220748225,"end":220784815,"strand":1,"description":"mitochondrial amidoxime reducing component 2 [Source:HGNC Symbol;Acc:HGNC:26064]"}, {"versioned_ensembl_gene_id":"ENSG00000230150.1","gene_symbol":"AL773543.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32646664,"end":32647494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225940.5","gene_symbol":"C5orf67","gene_name":"chromosome 5 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:51252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101928448","summary":null,"start":56511567,"end":56606232,"strand":-1,"description":"chromosome 5 open reading frame 67 [Source:HGNC Symbol;Acc:HGNC:51252]"}, {"versioned_ensembl_gene_id":"ENSG00000251539.1","gene_symbol":"SNX18P24","gene_name":"sorting nexin 18 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39632]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419004","summary":null,"start":49561479,"end":49562149,"strand":1,"description":"sorting nexin 18 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39632]"}, {"versioned_ensembl_gene_id":"ENSG00000239877.2","gene_symbol":"IGSF11-AS1","gene_name":"IGSF11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40777]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506765","summary":null,"start":118943073,"end":118948241,"strand":1,"description":"IGSF11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40777]"}, {"versioned_ensembl_gene_id":"ENSG00000233718.7","gene_symbol":"MYCNOS","gene_name":"MYCN opposite strand [Source:HGNC Symbol;Acc:HGNC:16911]","synonyms":"NCYM,N-CYM,MYCN-AS1","biotype":"antisense_RNA","ncbi_id":"10408","summary":"This gene is transcribed in antisense to the v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog gene (MYCN). It is thought to encode a small, novel protein that stabilizes MYCN, prevents apoptosis, and promotes cell proliferation. Transcripts at this locus may also act directly as functional RNAs to recruit transcriptional regulators to the promoter of MYCN and stimulate transcription of this oncogene. This gene therefore functions through both RNA and protein products. [provided by RefSeq, Aug 2016]","start":15921037,"end":15942249,"strand":-1,"description":"MYCN opposite strand [Source:HGNC Symbol;Acc:HGNC:16911]"}, {"versioned_ensembl_gene_id":"ENSG00000103091.14","gene_symbol":"WDR59","gene_name":"WD repeat domain 59 [Source:HGNC Symbol;Acc:HGNC:25706]","synonyms":"FLJ12270","biotype":"protein_coding","ncbi_id":"79726","summary":null,"start":74871367,"end":75000173,"strand":-1,"description":"WD repeat domain 59 [Source:HGNC Symbol;Acc:HGNC:25706]"}, {"versioned_ensembl_gene_id":"ENSG00000196366.3","gene_symbol":"C9orf163","gene_name":"chromosome 9 open reading frame 163 [Source:HGNC Symbol;Acc:HGNC:26718]","synonyms":"FLJ36779","biotype":"lincRNA","ncbi_id":"158055","summary":null,"start":136483495,"end":136486067,"strand":1,"description":"chromosome 9 open reading frame 163 [Source:HGNC Symbol;Acc:HGNC:26718]"}, {"versioned_ensembl_gene_id":"ENSG00000223457.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"HTATSF1P,dJ1033B10.6,TAT-SF1-L","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33237799,"end":33239690,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000259164.1","gene_symbol":"AC007375.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":77098311,"end":77225462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242352.2","gene_symbol":"FAM91A3P","gene_name":"family with sequence similarity 91 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32273]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729182","summary":null,"start":143766540,"end":143769083,"strand":1,"description":"family with sequence similarity 91 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:32273]"}, {"versioned_ensembl_gene_id":"ENSG00000232010.1","gene_symbol":"AP001059.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44250813,"end":44251520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232721.2","gene_symbol":"AC239800.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143736066,"end":143739506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197548.12","gene_symbol":"ATG7","gene_name":"autophagy related 7 [Source:HGNC Symbol;Acc:HGNC:16935]","synonyms":"GSA7,DKFZp434N0735,APG7L","biotype":"protein_coding","ncbi_id":"10533","summary":"This gene encodes an E1-like activating enzyme that is essential for autophagy and cytoplasmic to vacuole transport. The encoded protein is also thought to modulate p53-dependent cell cycle pathways during prolonged metabolic stress. It has been associated with multiple functions, including axon membrane trafficking, axonal homeostasis, mitophagy, adipose differentiation, and hematopoietic stem cell maintenance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":11272309,"end":11557665,"strand":1,"description":"autophagy related 7 [Source:HGNC Symbol;Acc:HGNC:16935]"}, {"versioned_ensembl_gene_id":"ENSG00000257829.1","gene_symbol":"AC121757.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52306616,"end":52308371,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271716.1","gene_symbol":"AC022001.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11607184,"end":11610748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206404.11","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31666915,"end":31674267,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000244124.1","gene_symbol":"ATP1B3-AS1","gene_name":"ATP1B3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40088]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874077","summary":null,"start":141918252,"end":141919021,"strand":-1,"description":"ATP1B3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40088]"}, {"versioned_ensembl_gene_id":"ENSG00000270641.1","gene_symbol":"TSIX","gene_name":"TSIX transcript, XIST antisense RNA [Source:HGNC Symbol;Acc:HGNC:12377]","synonyms":"XIST-AS1,NCRNA00013,LINC00013","biotype":"lincRNA","ncbi_id":"9383","summary":"In mammals, dosage compensation of genes on the X chromosome occurs by X inactivation, which is regulated in cis by the X-inactivation center (XIC) and expression of the XIST non-coding RNA. This gene expresses a non-coding antisense transcript across the 3' end of the XIST locus, and is coexpressed with XIST only from the inactive X chromosome. The mouse ortholog of this locus is required for imprinted X inactivation in extraembryonic tissues and silences Xist through modification of the chromatin structure in the Xist promoter region. In contrast, imprinted X inactivation does not occur in human extraembryonic tissues and transcripts from this locus do not repress XIST expression or affect random X chromosome inactivation in embryonic cells. This transcript is thought to be unspliced and extend over more than 30 kb, but its exact nature has not been determined. [provided by RefSeq, Jul 2008]","start":73792205,"end":73829231,"strand":1,"description":"TSIX transcript, XIST antisense RNA [Source:HGNC Symbol;Acc:HGNC:12377]"}, {"versioned_ensembl_gene_id":"ENSG00000226028.2","gene_symbol":"PFN1P12","gene_name":"profilin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42995]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647569","summary":null,"start":143619994,"end":143620527,"strand":1,"description":"profilin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42995]"}, {"versioned_ensembl_gene_id":"ENSG00000238280.1","gene_symbol":"AL133417.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62793562,"end":62805887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239268.2","gene_symbol":"AC092691.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117672154,"end":117997592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224098.1","gene_symbol":"BX120009.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33219899,"end":33220308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282379.1","gene_symbol":"DTX2","gene_name":"deltex E3 ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:15973]","synonyms":"RNF58,KIAA1528","biotype":"protein_coding","ncbi_id":"113878","summary":"DTX2 functions as an E3 ubiquitin ligase (Takeyama et al., 2003 [PubMed 12670957]).[supplied by OMIM, Nov 2009]","start":76501267,"end":76505995,"strand":1,"description":"deltex E3 ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:15973]"}, {"versioned_ensembl_gene_id":"ENSG00000245970.2","gene_symbol":"AP003352.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98041726,"end":98044121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227370.1","gene_symbol":"AC254562.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42132543,"end":42132998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281538.1","gene_symbol":"AC254562.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42138060,"end":42139726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270915.1","gene_symbol":"AC073410.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202505012,"end":202505343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225459.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":33050172,"end":33050246,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000110328.5","gene_symbol":"GALNT18","gene_name":"polypeptide N-acetylgalactosaminyltransferase 18 [Source:HGNC Symbol;Acc:HGNC:30488]","synonyms":"MGC71806,GALNTL4,GALNT15,GalNAc-T18","biotype":"protein_coding","ncbi_id":"374378","summary":null,"start":11270876,"end":11622005,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 18 [Source:HGNC Symbol;Acc:HGNC:30488]"}, {"versioned_ensembl_gene_id":"ENSG00000243423.1","gene_symbol":"AC004223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35076737,"end":35077007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109756.8","gene_symbol":"RAPGEF2","gene_name":"Rap guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:16854]","synonyms":"RA-GEF,PDZGEF1,PDZ-GEF1,KIAA0313,DKFZP586O1422","biotype":"protein_coding","ncbi_id":"9693","summary":"Members of the RAS (see HRAS; MIM 190020) subfamily of GTPases function in signal transduction as GTP/GDP-regulated switches that cycle between inactive GDP- and active GTP-bound states. Guanine nucleotide exchange factors (GEFs), such as RAPGEF2, serve as RAS activators by promoting acquisition of GTP to maintain the active GTP-bound state and are the key link between cell surface receptors and RAS activation (Rebhun et al., 2000 [PubMed 10934204]).[supplied by OMIM, Mar 2008]","start":159104178,"end":159360169,"strand":1,"description":"Rap guanine nucleotide exchange factor 2 [Source:HGNC Symbol;Acc:HGNC:16854]"}, {"versioned_ensembl_gene_id":"ENSG00000270648.1","gene_symbol":"CYP2C61P","gene_name":"cytochrome P450 family 2 subfamily C member 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:39972]","synonyms":"CYP2C-se2[1:2]","biotype":"processed_pseudogene","ncbi_id":"106480734","summary":null,"start":64762883,"end":64763172,"strand":-1,"description":"cytochrome P450 family 2 subfamily C member 61, pseudogene [Source:HGNC Symbol;Acc:HGNC:39972]"}, {"versioned_ensembl_gene_id":"ENSG00000237427.1","gene_symbol":"TOMM22P1","gene_name":"TOMM22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38736]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499416","summary":null,"start":21130870,"end":21131181,"strand":1,"description":"TOMM22 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38736]"}, {"versioned_ensembl_gene_id":"ENSG00000166569.8","gene_symbol":"CPLX4","gene_name":"complexin 4 [Source:HGNC Symbol;Acc:HGNC:24330]","synonyms":"CPX-IV","biotype":"protein_coding","ncbi_id":"339302","summary":"This gene likely encodes a member of the complexin family. The encoded protein may be involved in synaptic vesicle exocytosis. [provided by RefSeq, Jan 2009]","start":59275156,"end":59318649,"strand":-1,"description":"complexin 4 [Source:HGNC Symbol;Acc:HGNC:24330]"}, {"versioned_ensembl_gene_id":"ENSG00000235627.1","gene_symbol":"SNRPFP4","gene_name":"small nuclear ribonucleoprotein polypeptide F pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39667]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874412","summary":null,"start":48161176,"end":48161417,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide F pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39667]"}, {"versioned_ensembl_gene_id":"ENSG00000112796.9","gene_symbol":"ENPP5","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 5 (putative) [Source:HGNC Symbol;Acc:HGNC:13717]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59084","summary":"This gene encodes a type-I transmembrane glycoprotein. Studies in rat suggest the encoded protein may play a role in neuronal cell communications. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2014]","start":46159187,"end":46170971,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 5 (putative) [Source:HGNC Symbol;Acc:HGNC:13717]"}, {"versioned_ensembl_gene_id":"ENSG00000279616.1","gene_symbol":"AL096817.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87356831,"end":87358605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151033.8","gene_symbol":"LYZL2","gene_name":"lysozyme like 2 [Source:HGNC Symbol;Acc:HGNC:29613]","synonyms":null,"biotype":"protein_coding","ncbi_id":"119180","summary":"Lysozymes (see LYZ; MIM 153450), especially C-type lysozymes, are well-recognized bacteriolytic factors widely distributed in the animal kingdom and play a mainly protective role in host defense. LYZL2 is a member of a family of lysozyme-like genes (Zhang et al., 2005 [PubMed 16014814]).[supplied by OMIM, Apr 2009]","start":30611779,"end":30629762,"strand":-1,"description":"lysozyme like 2 [Source:HGNC Symbol;Acc:HGNC:29613]"}, {"versioned_ensembl_gene_id":"ENSG00000226504.1","gene_symbol":"TMEM167AP1","gene_name":"transmembrane protein 167A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23956]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360028","summary":null,"start":20907344,"end":20907562,"strand":-1,"description":"transmembrane protein 167A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23956]"}, {"versioned_ensembl_gene_id":"ENSG00000271151.1","gene_symbol":"AC016737.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173968351,"end":173969418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162817.6","gene_symbol":"C1orf115","gene_name":"chromosome 1 open reading frame 115 [Source:HGNC Symbol;Acc:HGNC:25873]","synonyms":"FLJ14146","biotype":"protein_coding","ncbi_id":"79762","summary":null,"start":220689845,"end":220699157,"strand":1,"description":"chromosome 1 open reading frame 115 [Source:HGNC Symbol;Acc:HGNC:25873]"}, {"versioned_ensembl_gene_id":"ENSG00000156959.8","gene_symbol":"LHFPL4","gene_name":"LHFPL tetraspan subfamily member 4 [Source:HGNC Symbol;Acc:HGNC:29568]","synonyms":null,"biotype":"protein_coding","ncbi_id":"375323","summary":"This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. [provided by RefSeq, Jul 2008]","start":9498361,"end":9553802,"strand":-1,"description":"LHFPL tetraspan subfamily member 4 [Source:HGNC Symbol;Acc:HGNC:29568]"}, {"versioned_ensembl_gene_id":"ENSG00000277541.1","gene_symbol":"ZNF630-AS1","gene_name":"ZNF630 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41215]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874120","summary":null,"start":48056310,"end":48066583,"strand":1,"description":"ZNF630 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41215]"}, {"versioned_ensembl_gene_id":"ENSG00000266086.1","gene_symbol":"AC015813.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57989038,"end":58005253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279924.1","gene_symbol":"AL356585.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18174010,"end":18178465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217805.2","gene_symbol":"AL590084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25181359,"end":25181745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236278.2","gene_symbol":"PEBP1P3","gene_name":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129570","summary":null,"start":198679139,"end":198680033,"strand":-1,"description":"phosphatidylethanolamine binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44345]"}, {"versioned_ensembl_gene_id":"ENSG00000237530.1","gene_symbol":"AL136140.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44525259,"end":44526754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223430.1","gene_symbol":"AC011243.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133554315,"end":133558227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096401.7","gene_symbol":"CDC5L","gene_name":"cell division cycle 5 like [Source:HGNC Symbol;Acc:HGNC:1743]","synonyms":"PCDC5RP,hCDC5,CEF1,CDC5","biotype":"protein_coding","ncbi_id":"988","summary":"The protein encoded by this gene shares a significant similarity with Schizosaccharomyces pombe cdc5 gene product, which is a cell cycle regulator important for G2/M transition. This protein has been demonstrated to act as a positive regulator of cell cycle G2/M progression. It was also found to be an essential component of a non-snRNA spliceosome, which contains at least five additional protein factors and is required for the second catalytic step of pre-mRNA splicing. [provided by RefSeq, Jul 2008]","start":44387525,"end":44450426,"strand":1,"description":"cell division cycle 5 like [Source:HGNC Symbol;Acc:HGNC:1743]"}, {"versioned_ensembl_gene_id":"ENSG00000213355.3","gene_symbol":"CNN2P8","gene_name":"calponin 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39533]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"205272","summary":null,"start":94737337,"end":94738249,"strand":1,"description":"calponin 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39533]"}, {"versioned_ensembl_gene_id":"ENSG00000204764.13","gene_symbol":"RANBP17","gene_name":"RAN binding protein 17 [Source:HGNC Symbol;Acc:HGNC:14428]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64901","summary":"The transport of protein and large RNAs through the nuclear pore complexes (NPC) is an energy-dependent and regulated process. The import of proteins with a nuclear localization signal (NLS) is accomplished by recognition of one or more clusters of basic amino acids by the importin-alpha/beta complex; see MIM 600685 and MIM 602738. The small GTPase RAN (MIM 601179) plays a key role in NLS-dependent protein import. RAN-binding protein-17 is a member of the importin-beta superfamily of nuclear transport receptors.[supplied by OMIM, Jul 2002]","start":170861870,"end":171300015,"strand":1,"description":"RAN binding protein 17 [Source:HGNC Symbol;Acc:HGNC:14428]"}, {"versioned_ensembl_gene_id":"ENSG00000175573.6","gene_symbol":"C11orf68","gene_name":"chromosome 11 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:28801]","synonyms":"P5326,BLES03","biotype":"protein_coding","ncbi_id":"83638","summary":null,"start":65916808,"end":65919117,"strand":-1,"description":"chromosome 11 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:28801]"}, {"versioned_ensembl_gene_id":"ENSG00000269533.5","gene_symbol":"AC003002.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57389884,"end":57419994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106546.12","gene_symbol":"AHR","gene_name":"aryl hydrocarbon receptor [Source:HGNC Symbol;Acc:HGNC:348]","synonyms":"bHLHe76","biotype":"protein_coding","ncbi_id":"196","summary":"The protein encoded by this gene is a ligand-activated helix-loop-helix transcription factor involved in the regulation of biological responses to planar aromatic hydrocarbons. This receptor has been shown to regulate xenobiotic-metabolizing enzymes such as cytochrome P450. Before ligand binding, the encoded protein is sequestered in the cytoplasm; upon ligand binding, this protein moves to the nucleus and stimulates transcription of target genes. [provided by RefSeq, Sep 2015]","start":17298622,"end":17346152,"strand":1,"description":"aryl hydrocarbon receptor [Source:HGNC Symbol;Acc:HGNC:348]"}, {"versioned_ensembl_gene_id":"ENSG00000244712.1","gene_symbol":"AC084754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28564678,"end":28565141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278733.1","gene_symbol":"AC022079.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28185625,"end":28186190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242485.5","gene_symbol":"MRPL20","gene_name":"mitochondrial ribosomal protein L20 [Source:HGNC Symbol;Acc:HGNC:14478]","synonyms":"FLJ10024","biotype":"protein_coding","ncbi_id":"55052","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 21q. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":1401908,"end":1407313,"strand":-1,"description":"mitochondrial ribosomal protein L20 [Source:HGNC Symbol;Acc:HGNC:14478]"}, {"versioned_ensembl_gene_id":"ENSG00000225582.1","gene_symbol":"AC011193.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34479312,"end":34479957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004776.12","gene_symbol":"HSPB6","gene_name":"heat shock protein family B (small) member 6 [Source:HGNC Symbol;Acc:HGNC:26511]","synonyms":"PPP1R91,Hsp20,FLJ32389","biotype":"protein_coding","ncbi_id":"126393","summary":"This locus encodes a heat shock protein. The encoded protein likely plays a role in smooth muscle relaxation. [provided by RefSeq, Jan 2012]","start":35754569,"end":35758079,"strand":-1,"description":"heat shock protein family B (small) member 6 [Source:HGNC Symbol;Acc:HGNC:26511]"}, {"versioned_ensembl_gene_id":"ENSG00000161031.12","gene_symbol":"PGLYRP2","gene_name":"peptidoglycan recognition protein 2 [Source:HGNC Symbol;Acc:HGNC:30013]","synonyms":"PGRP-L,PGLYRPL,TAGL-like,tagl-beta,tagL-alpha,tagL,PGRPL","biotype":"protein_coding","ncbi_id":"114770","summary":"This gene encodes a peptidoglycan recognition protein, which belongs to the N-acetylmuramoyl-L-alanine amidase 2 family. This protein hydrolyzes the link between N-acetylmuramoyl residues and L-amino acid residues in bacterial cell wall glycopeptides, and thus may play a scavenger role by digesting biologically active peptidoglycan into biologically inactive fragments. [provided by RefSeq, Sep 2011]","start":15468645,"end":15498956,"strand":-1,"description":"peptidoglycan recognition protein 2 [Source:HGNC Symbol;Acc:HGNC:30013]"}, {"versioned_ensembl_gene_id":"ENSG00000105953.14","gene_symbol":"OGDH","gene_name":"oxoglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8124]","synonyms":"E1k","biotype":"protein_coding","ncbi_id":"4967","summary":"This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]","start":44606572,"end":44709066,"strand":1,"description":"oxoglutarate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8124]"}, {"versioned_ensembl_gene_id":"ENSG00000204816.5","gene_symbol":"FGF7P5","gene_name":"fibroblast growth factor 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33588]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653453","summary":null,"start":42625436,"end":42626813,"strand":1,"description":"fibroblast growth factor 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33588]"}, {"versioned_ensembl_gene_id":"ENSG00000269961.1","gene_symbol":"AC010359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65924629,"end":65925135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280529.2","gene_symbol":"TAF4","gene_name":"TATA-box binding protein associated factor 4 [Source:HGNC Symbol;Acc:HGNC:11537]","synonyms":"TAFII135,TAFII130,TAF4A,TAF2C1,TAF2C","biotype":"protein_coding","ncbi_id":"6874","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the larger subunits of TFIID that has been shown to potentiate transcriptional activation by retinoic acid, thyroid hormone and vitamin D3 receptors. In addition, this subunit interacts with the transcription factor CREB, which has a glutamine-rich activation domain, and binds to other proteins containing glutamine-rich regions. Aberrant binding to this subunit by proteins with expanded polyglutamine regions has been suggested as one of the pathogenetic mechanisms underlying a group of neurodegenerative disorders referred to as polyglutamine diseases. [provided by RefSeq, Jul 2008]","start":61950345,"end":62005079,"strand":-1,"description":"TATA-box binding protein associated factor 4 [Source:HGNC Symbol;Acc:HGNC:11537]"}, {"versioned_ensembl_gene_id":"ENSG00000116218.12","gene_symbol":"NPHS2","gene_name":"NPHS2, podocin [Source:HGNC Symbol;Acc:HGNC:13394]","synonyms":"SRN1,PDCN","biotype":"protein_coding","ncbi_id":"7827","summary":"This gene encodes a protein that plays a role in the regulation of glomerular permeability. Mutations in this gene cause steroid-resistant nephrotic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":179550539,"end":179575952,"strand":-1,"description":"NPHS2, podocin [Source:HGNC Symbol;Acc:HGNC:13394]"}, {"versioned_ensembl_gene_id":"ENSG00000258488.2","gene_symbol":"AC023310.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20516252,"end":20520627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247081.7","gene_symbol":"BAALC-AS1","gene_name":"BAALC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50461]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100499183","summary":null,"start":103156990,"end":103298772,"strand":-1,"description":"BAALC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50461]"}, {"versioned_ensembl_gene_id":"ENSG00000244226.1","gene_symbol":"ILF2P1","gene_name":"interleukin enhancer binding factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421506","summary":null,"start":65687301,"end":65688468,"strand":1,"description":"interleukin enhancer binding factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44695]"}, {"versioned_ensembl_gene_id":"ENSG00000240175.1","gene_symbol":"MAGI1-AS1","gene_name":"MAGI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40091]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873983","summary":null,"start":65893816,"end":65925297,"strand":1,"description":"MAGI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40091]"}, {"versioned_ensembl_gene_id":"ENSG00000255153.1","gene_symbol":"TOLLIP-AS1","gene_name":"TOLLIP antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27403]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"255512","summary":null,"start":1309769,"end":1310707,"strand":1,"description":"TOLLIP antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27403]"}, {"versioned_ensembl_gene_id":"ENSG00000236808.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"tctex-6,hZR14,RPA12,HTEX-6","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30137399,"end":30143406,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000099139.13","gene_symbol":"PCSK5","gene_name":"proprotein convertase subtilisin/kexin type 5 [Source:HGNC Symbol;Acc:HGNC:8747]","synonyms":"SPC6,PC6,PC5","biotype":"protein_coding","ncbi_id":"5125","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER. It then sorts to the trans-Golgi network where a second autocatalytic event takes place and the catalytic activity is acquired. This encoded protein is widely expressed and one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It mediates posttranslational endoproteolytic processing for several integrin alpha subunits and is thought to process prorenin, pro-membrane type-1 matrix metalloproteinase and HIV-1 glycoprotein gp160. Alternative splicing results in multiple transcript variants, some of which encode distinct isoforms, including a protease packaged into dense core granules (PC5A) and a type 1 membrane bound protease (PC5B). [provided by RefSeq, May 2014]","start":75890644,"end":76362339,"strand":1,"description":"proprotein convertase subtilisin/kexin type 5 [Source:HGNC Symbol;Acc:HGNC:8747]"}, {"versioned_ensembl_gene_id":"ENSG00000205502.3","gene_symbol":"C2CD4B","gene_name":"C2 calcium dependent domain containing 4B [Source:HGNC Symbol;Acc:HGNC:33628]","synonyms":"NLF2,FAM148B","biotype":"protein_coding","ncbi_id":"388125","summary":null,"start":62163535,"end":62165283,"strand":-1,"description":"C2 calcium dependent domain containing 4B [Source:HGNC Symbol;Acc:HGNC:33628]"}, {"versioned_ensembl_gene_id":"ENSG00000162772.16","gene_symbol":"ATF3","gene_name":"activating transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:785]","synonyms":null,"biotype":"protein_coding","ncbi_id":"467","summary":"This gene encodes a member of the mammalian activation transcription factor/cAMP responsive element-binding (CREB) protein family of transcription factors. This gene is induced by a variety of signals, including many of those encountered by cancer cells, and is involved in the complex process of cellular stress response. Multiple transcript variants encoding different isoforms have been found for this gene. It is possible that alternative splicing of this gene may be physiologically important in the regulation of target genes. [provided by RefSeq, Apr 2011]","start":212565334,"end":212620777,"strand":1,"description":"activating transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:785]"}, {"versioned_ensembl_gene_id":"ENSG00000256072.1","gene_symbol":"AC078889.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66251745,"end":66257434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233728.1","gene_symbol":"AL929472.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37799720,"end":37800879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236833.1","gene_symbol":"AC024560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197660565,"end":197665757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124635.8","gene_symbol":"HIST1H2BJ","gene_name":"histone cluster 1 H2B family member j [Source:HGNC Symbol;Acc:HGNC:4761]","synonyms":"H2BFR,H2B/r","biotype":"protein_coding","ncbi_id":"8970","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]","start":27125897,"end":27132750,"strand":-1,"description":"histone cluster 1 H2B family member j [Source:HGNC Symbol;Acc:HGNC:4761]"}, {"versioned_ensembl_gene_id":"ENSG00000185090.14","gene_symbol":"MANEAL","gene_name":"mannosidase endo-alpha like [Source:HGNC Symbol;Acc:HGNC:26452]","synonyms":"FLJ31434","biotype":"protein_coding","ncbi_id":"149175","summary":null,"start":37793802,"end":37801137,"strand":1,"description":"mannosidase endo-alpha like [Source:HGNC Symbol;Acc:HGNC:26452]"}, {"versioned_ensembl_gene_id":"ENSG00000196072.11","gene_symbol":"BLOC1S2","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:20984]","synonyms":"MGC10120,FLJ30135,BORCS2,BLOS2","biotype":"protein_coding","ncbi_id":"282991","summary":"This gene encodes a protein with multiple functions. The encoded protein has been found in association with the centrosome, shown to co-localize with gamma-tubulin, and also found to be one of the proteins in the BLOC-1 complex which functions in the formation of lysosome-related organelles. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":100273280,"end":100286712,"strand":-1,"description":"biogenesis of lysosomal organelles complex 1 subunit 2 [Source:HGNC Symbol;Acc:HGNC:20984]"}, {"versioned_ensembl_gene_id":"ENSG00000052795.12","gene_symbol":"FNIP2","gene_name":"folliculin interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29280]","synonyms":"MAPO1,KIAA1450,FNIPL","biotype":"protein_coding","ncbi_id":"57600","summary":"This gene encodes a protein that binds to the tumor suppressor folliculin and to AMP-activated protein kinase (AMPK), and may play a role cellular metabolism and nutrient sensing by regulating the AMPK-mechanistic target of rapamycin signaling pathway. The encoded protein may also be involved in regulating the O6-methylguanine-induced apoptosis signaling pathway. This gene has a closely related paralog that encodes a protein with similar binding activities. Both related proteins also associate with the molecular chaperone heat shock protein-90 (Hsp90) and negatively regulate its ATPase activity and facilitate its association with folliculin. [provided by RefSeq, Jul 2017]","start":158769138,"end":158908049,"strand":1,"description":"folliculin interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:29280]"}, {"versioned_ensembl_gene_id":"ENSG00000255317.1","gene_symbol":"AP002833.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126992452,"end":126995458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076555.15","gene_symbol":"ACACB","gene_name":"acetyl-CoA carboxylase beta [Source:HGNC Symbol;Acc:HGNC:85]","synonyms":"HACC275,ACCB,ACC2","biotype":"protein_coding","ncbi_id":"32","summary":" Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. ACC-beta is thought to control fatty acid oxidation by means of the ability of malonyl-CoA to inhibit carnitine-palmitoyl-CoA transferase I, the rate-limiting step in fatty acid uptake and oxidation by mitochondria. ACC-beta may be involved in the regulation of fatty acid oxidation, rather than fatty acid biosynthesis. There is evidence for the presence of two ACC-beta isoforms. [provided by RefSeq, Jul 2008]","start":109116595,"end":109268226,"strand":1,"description":"acetyl-CoA carboxylase beta [Source:HGNC Symbol;Acc:HGNC:85]"}, {"versioned_ensembl_gene_id":"ENSG00000273450.1","gene_symbol":"AL139124.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94314907,"end":94315327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242880.1","gene_symbol":"AC046136.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115251196,"end":115285347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223495.2","gene_symbol":"AC239859.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143498785,"end":143499102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277768.2","gene_symbol":"CCL3L3","gene_name":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]","synonyms":"MGC12815","biotype":"protein_coding","ncbi_id":"414062","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this gene binds to several chemokine receptors, including chemokine binding protein 2 and chemokine (C-C motif) receptor 5 (CCR5). CCR5 is a co-receptor for HIV, and binding of this protein to CCR5 inhibits HIV entry. The copy number of this gene varies among individuals, where most individuals have one to six copies, and a minority of individuals have zero or more than six copies. There are conflicting reports about copy number variation of this gene and its correlation to disease susceptibility.[provided by RefSeq, Apr 2014]","start":36296480,"end":36298369,"strand":-1,"description":"C-C motif chemokine ligand 3 like 3 [Source:HGNC Symbol;Acc:HGNC:30554]"}, {"versioned_ensembl_gene_id":"ENSG00000229816.1","gene_symbol":"DDX50P1","gene_name":"DEAD-box helicase 50 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192146","summary":null,"start":32201600,"end":32203999,"strand":1,"description":"DEAD-box helicase 50 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18974]"}, {"versioned_ensembl_gene_id":"ENSG00000179698.13","gene_symbol":"WDR97","gene_name":"WD repeat domain 97 [Source:HGNC Symbol;Acc:HGNC:26959]","synonyms":"KIAA1875","biotype":"protein_coding","ncbi_id":"340390","summary":"The function and protein-coding potential of this gene is unknown. The exon combination is based on AB058778.1 for which two possible open reading frames can be predicted (with start codons at nucleotide 26 or 2614). The position of the first ORF stop codon is consistent with a prediction of nonsense-mediated decay. Given the observation of the first ORF and its length, a predicted translation of the second ORF is inconsistent with the translation leaky scanning theory. Therefore, this gene is represented as a non-protein-coding transcript. [provided by RefSeq, Oct 2008]","start":144107726,"end":144118315,"strand":1,"description":"WD repeat domain 97 [Source:HGNC Symbol;Acc:HGNC:26959]"}, {"versioned_ensembl_gene_id":"ENSG00000174227.15","gene_symbol":"PIGG","gene_name":"phosphatidylinositol glycan anchor biosynthesis class G [Source:HGNC Symbol;Acc:HGNC:25985]","synonyms":"GPI7,FLJ20265,LAS21","biotype":"protein_coding","ncbi_id":"54872","summary":"This gene encodes an enzyme involved in glycosylphosphatidylinositol-anchor biosynthesis. The encoded protein, which is localized to the endoplasmic reticulum, is involved in transferring ethanoloamine phosphate to mannose 2 of glycosylphosphatidylinositol species H7 to form species H8. Allelic variants of this gene have been associated with intellectual disability, hypotonia, and early-onset seizures. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":499210,"end":540196,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class G [Source:HGNC Symbol;Acc:HGNC:25985]"}, {"versioned_ensembl_gene_id":"ENSG00000226058.1","gene_symbol":"AC092570.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101375587,"end":101376055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105146.12","gene_symbol":"AURKC","gene_name":"aurora kinase C [Source:HGNC Symbol;Acc:HGNC:11391]","synonyms":"STK13,AurC,ARK3","biotype":"protein_coding","ncbi_id":"6795","summary":"This gene encodes a member of the Aurora subfamily of serine/threonine protein kinases. The encoded protein is a chromosomal passenger protein that forms complexes with Aurora-B and inner centromere proteins and may play a role in organizing microtubules in relation to centrosome/spindle function during mitosis. This gene is overexpressed in several cancer cell lines, suggesting an involvement in oncogenic signal transduction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":57230802,"end":57235548,"strand":1,"description":"aurora kinase C [Source:HGNC Symbol;Acc:HGNC:11391]"}, {"versioned_ensembl_gene_id":"ENSG00000139800.8","gene_symbol":"ZIC5","gene_name":"Zic family member 5 [Source:HGNC Symbol;Acc:HGNC:20322]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85416","summary":"This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. The encoded protein may act as a transcriptional repressor. Studies in mouse and Xenopus support a role for this gene in neural crest development. Elevated expression of this gene has been observed in various human cancers and may contribute to cancer progression. This gene is closely linked to a related family member on chromosome 13. [provided by RefSeq, Mar 2017]","start":99962964,"end":99971909,"strand":-1,"description":"Zic family member 5 [Source:HGNC Symbol;Acc:HGNC:20322]"}, {"versioned_ensembl_gene_id":"ENSG00000229742.1","gene_symbol":"AC092809.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":224297646,"end":224298600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182108.9","gene_symbol":"DEXI","gene_name":"Dexi homolog [Source:HGNC Symbol;Acc:HGNC:13267]","synonyms":"MYLE","biotype":"protein_coding","ncbi_id":"28955","summary":null,"start":10928891,"end":10942460,"strand":-1,"description":"Dexi homolog [Source:HGNC Symbol;Acc:HGNC:13267]"}, {"versioned_ensembl_gene_id":"ENSG00000275673.1","gene_symbol":"AC133065.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":10934258,"end":10934887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280153.1","gene_symbol":"AC133065.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10933903,"end":10936280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234218.9","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31485545,"end":31498583,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000062598.17","gene_symbol":"ELMO2","gene_name":"engulfment and cell motility 2 [Source:HGNC Symbol;Acc:HGNC:17233]","synonyms":"FLJ11656,KIAA1834,ELMO-2,CED12,CED-12","biotype":"protein_coding","ncbi_id":"63916","summary":"The protein encoded by this gene interacts with the dedicator of cyto-kinesis 1 protein. Similarity to a C. elegans protein suggests that this protein may function in phagocytosis of apoptotic cells and in cell migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":46366049,"end":46432985,"strand":-1,"description":"engulfment and cell motility 2 [Source:HGNC Symbol;Acc:HGNC:17233]"}, {"versioned_ensembl_gene_id":"ENSG00000230863.2","gene_symbol":"AL096829.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75641346,"end":75642087,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271397.1","gene_symbol":"AL109837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11608436,"end":11609048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274212.1","gene_symbol":"AL365265.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16041381,"end":16041614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232947.1","gene_symbol":"LINC02543","gene_name":"long intergenic non-protein coding RNA 2543 [Source:HGNC Symbol;Acc:HGNC:53577]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928406","summary":null,"start":15994944,"end":15999797,"strand":1,"description":"long intergenic non-protein coding RNA 2543 [Source:HGNC Symbol;Acc:HGNC:53577]"}, {"versioned_ensembl_gene_id":"ENSG00000214027.3","gene_symbol":"ARPC3P5","gene_name":"actin related protein 2/3 complex subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39435]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441131","summary":null,"start":15934782,"end":15935315,"strand":1,"description":"actin related protein 2/3 complex subunit 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39435]"}, {"versioned_ensembl_gene_id":"ENSG00000280592.2","gene_symbol":"LINC01624","gene_name":"long intergenic non-protein coding RNA 1624 [Source:HGNC Symbol;Acc:HGNC:52051]","synonyms":"TCONS_00011425","biotype":"lincRNA","ncbi_id":"401289","summary":null,"start":170272763,"end":170279887,"strand":1,"description":"long intergenic non-protein coding RNA 1624 [Source:HGNC Symbol;Acc:HGNC:52051]"}, {"versioned_ensembl_gene_id":"ENSG00000282473.1","gene_symbol":"IGHVIII-76-1","gene_name":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]","synonyms":"IGHV(III)-76-1","biotype":"IG_V_pseudogene","ncbi_id":"28339","summary":null,"start":106855943,"end":106856228,"strand":-1,"description":"immunoglobulin heavy variable (III)-76-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5708]"}, {"versioned_ensembl_gene_id":"ENSG00000276060.2","gene_symbol":"IGHV3-75","gene_name":"immunoglobulin heavy variable 3-75 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5625]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28407","summary":null,"start":106847863,"end":106848323,"strand":-1,"description":"immunoglobulin heavy variable 3-75 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5625]"}, {"versioned_ensembl_gene_id":"ENSG00000183291.15","gene_symbol":"SELENOF","gene_name":"selenoprotein F [Source:HGNC Symbol;Acc:HGNC:17705]","synonyms":"SEP15","biotype":"protein_coding","ncbi_id":"9403","summary":"The protein encoded by this gene belongs to the SEP15/selenoprotein M family. The exact function of this protein is not known; however, it has been found to associate with UDP-glucose:glycoprotein glucosyltransferase (UGTR), an endoplasmic reticulum(ER)-resident protein, which is involved in the quality control of protein folding. The association with UGTR retains this protein in the ER, where it may play a role in protein folding. It has also been suggested to have a role in cancer etiology. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2016]","start":86862445,"end":86914424,"strand":-1,"description":"selenoprotein F [Source:HGNC Symbol;Acc:HGNC:17705]"}, {"versioned_ensembl_gene_id":"ENSG00000238008.1","gene_symbol":"COX6CP10","gene_name":"cytochrome c oxidase subunit 6C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481681","summary":null,"start":33554636,"end":33554859,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49362]"}, {"versioned_ensembl_gene_id":"ENSG00000271399.1","gene_symbol":"AL078624.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":228858010,"end":228858556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234539.9","gene_symbol":"ATF6B","gene_name":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]","synonyms":"G13,CREBL1","biotype":"protein_coding","ncbi_id":"1388","summary":"The protein encoded by this gene is a transcription factor in the unfolded protein response (UPR) pathway during ER stress. Either as a homodimer or as a heterodimer with ATF6-alpha, the encoded protein binds to the ER stress response element, interacting with nuclear transcription factor Y to activate UPR target genes. The protein is normally found in the membrane of the endoplasmic reticulum; however, under ER stress, the N-terminal cytoplasmic domain is cleaved from the rest of the protein and translocates to the nucleus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":32063716,"end":32076703,"strand":-1,"description":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]"}, {"versioned_ensembl_gene_id":"ENSG00000267758.1","gene_symbol":"AC099811.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42268587,"end":42269807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279245.1","gene_symbol":"FAM223A","gene_name":"family with sequence similarity 223 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30612]","synonyms":"SPCX,NCRNA00204A,NCRNA00204,LINC00204A,CXorf52","biotype":"lincRNA","ncbi_id":"100132967","summary":null,"start":154571248,"end":154571960,"strand":1,"description":"family with sequence similarity 223 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30612]"}, {"versioned_ensembl_gene_id":"ENSG00000266968.2","gene_symbol":"AC023421.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45646153,"end":45647937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112769.18","gene_symbol":"LAMA4","gene_name":"laminin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6484]","synonyms":"LAMA3","biotype":"protein_coding","ncbi_id":"3910","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the alpha chain isoform laminin, alpha 4. The domain structure of alpha 4 is similar to that of alpha 3, both of which resemble truncated versions of alpha 1 and alpha 2, in that approximately 1,200 residues at the N-terminus (domains IV, V and VI) have been lost. Laminin, alpha 4 contains the C-terminal G domain which distinguishes all alpha chains from the beta and gamma chains. The RNA analysis from adult and fetal tissues revealed developmental regulation of expression, however, the exact function of laminin, alpha 4 is not known. Tissue-specific utilization of alternative polyA-signal has been described in literature. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2011]","start":112108760,"end":112254939,"strand":-1,"description":"laminin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6484]"}, {"versioned_ensembl_gene_id":"ENSG00000164615.4","gene_symbol":"CAMLG","gene_name":"calcium modulating ligand [Source:HGNC Symbol;Acc:HGNC:1471]","synonyms":"GET2,CAML","biotype":"protein_coding","ncbi_id":"819","summary":"The immunosuppressant drug cyclosporin A blocks a calcium-dependent signal from the T-cell receptor (TCR) that normally leads to T-cell activation. When bound to cyclophilin B, cyclosporin A binds and inactivates the key signaling intermediate calcineurin. The protein encoded by this gene functions similarly to cyclosporin A, binding to cyclophilin B and acting downstream of the TCR and upstream of calcineurin by causing an influx of calcium. This integral membrane protein appears to be a new participant in the calcium signal transduction pathway, implicating cyclophilin B in calcium signaling, even in the absence of cyclosporin. [provided by RefSeq, Jul 2008]","start":134738501,"end":134752160,"strand":1,"description":"calcium modulating ligand [Source:HGNC Symbol;Acc:HGNC:1471]"}, {"versioned_ensembl_gene_id":"ENSG00000282399.1","gene_symbol":"AC242528.1","gene_name":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106786363,"end":106786859,"strand":-1,"description":"Immunoglobulin heavy variable 1-69D [Source:UniProtKB/Swiss-Prot;Acc:A0A0B4J2H0]"}, {"versioned_ensembl_gene_id":"ENSG00000110063.8","gene_symbol":"DCPS","gene_name":"decapping enzyme, scavenger [Source:HGNC Symbol;Acc:HGNC:29812]","synonyms":"HSPC015,HSL1,HINT-5","biotype":"protein_coding","ncbi_id":"28960","summary":"This gene encodes a member of the histidine triad family of pyrophosphatases that removes short mRNA fragments containing the 5′ mRNA cap structure, which appear in the 3′ → 5′ mRNA decay pathway, following deadenylation and exosome-mediated turnover. This enzyme hydrolyzes the triphosphate linkage of the cap structure (7-methylguanosine nucleoside triphosphate) to yield 7-methylguanosine monophosphate and nucleoside diphosphate. It protects the cell from the potentially toxic accumulation of these short, capped mRNA fragments, and regulates the activity of other cap-binding proteins, which are inhibited by their accumulation. It also acts as a transcript-specific modulator of pre-mRNA splicing and microRNA turnover. [provided by RefSeq, Apr 2017]","start":126303752,"end":126345749,"strand":1,"description":"decapping enzyme, scavenger [Source:HGNC Symbol;Acc:HGNC:29812]"}, {"versioned_ensembl_gene_id":"ENSG00000247363.2","gene_symbol":"AC090061.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68674371,"end":68687755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241825.2","gene_symbol":"RPL7P42","gene_name":"ribosomal protein L7 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:35543]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271223","summary":null,"start":68684595,"end":68686308,"strand":1,"description":"ribosomal protein L7 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:35543]"}, {"versioned_ensembl_gene_id":"ENSG00000280832.1","gene_symbol":"GSEC","gene_name":"G-quadruplex forming sequence containing lncRNA [Source:HGNC Symbol;Acc:HGNC:48645]","synonyms":"ST3GAL4-AS1,FLJ39051,DCPS-AS1","biotype":"antisense_RNA","ncbi_id":"399972","summary":null,"start":126340889,"end":126355587,"strand":-1,"description":"G-quadruplex forming sequence containing lncRNA [Source:HGNC Symbol;Acc:HGNC:48645]"}, {"versioned_ensembl_gene_id":"ENSG00000096060.14","gene_symbol":"FKBP5","gene_name":"FK506 binding protein 5 [Source:HGNC Symbol;Acc:HGNC:3721]","synonyms":"FKBP51,Ptg-10,PPIase,P54,FKBP54","biotype":"protein_coding","ncbi_id":"2289","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds to the immunosuppressants FK506 and rapamycin. It is thought to mediate calcineurin inhibition. It also interacts functionally with mature hetero-oligomeric progesterone receptor complexes along with the 90 kDa heat shock protein and P23 protein. This gene has been found to have multiple polyadenylation sites. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]","start":35573585,"end":35728583,"strand":-1,"description":"FK506 binding protein 5 [Source:HGNC Symbol;Acc:HGNC:3721]"}, {"versioned_ensembl_gene_id":"ENSG00000140987.19","gene_symbol":"ZSCAN32","gene_name":"zinc finger and SCAN domain containing 32 [Source:HGNC Symbol;Acc:HGNC:20812]","synonyms":"FLJ20417,ZNF434","biotype":"protein_coding","ncbi_id":"54925","summary":null,"start":3382081,"end":3401065,"strand":-1,"description":"zinc finger and SCAN domain containing 32 [Source:HGNC Symbol;Acc:HGNC:20812]"}, {"versioned_ensembl_gene_id":"ENSG00000232196.3","gene_symbol":"MTRNR2L4","gene_name":"MT-RNR2-like 4 [Source:HGNC Symbol;Acc:HGNC:37161]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463285","summary":null,"start":3370979,"end":3372740,"strand":-1,"description":"MT-RNR2-like 4 [Source:HGNC Symbol;Acc:HGNC:37161]"}, {"versioned_ensembl_gene_id":"ENSG00000225925.1","gene_symbol":"AL672138.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68474710,"end":68476874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254831.1","gene_symbol":"KRT18P58","gene_name":"keratin 18 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:48885]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644030","summary":null,"start":5993876,"end":5994995,"strand":-1,"description":"keratin 18 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:48885]"}, {"versioned_ensembl_gene_id":"ENSG00000229970.3","gene_symbol":"AC007128.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8262264,"end":8344516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278467.1","gene_symbol":"AC138393.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":223994262,"end":223995196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248744.1","gene_symbol":"AC108467.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45009540,"end":45051652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105732.12","gene_symbol":"ZNF574","gene_name":"zinc finger protein 574 [Source:HGNC Symbol;Acc:HGNC:26166]","synonyms":"FLJ22059","biotype":"protein_coding","ncbi_id":"64763","summary":null,"start":42068477,"end":42081549,"strand":1,"description":"zinc finger protein 574 [Source:HGNC Symbol;Acc:HGNC:26166]"}, {"versioned_ensembl_gene_id":"ENSG00000265752.2","gene_symbol":"AC010754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23957754,"end":23982556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250483.1","gene_symbol":"PPM1AP1","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30175]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"137012","summary":null,"start":15806149,"end":15807283,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30175]"}, {"versioned_ensembl_gene_id":"ENSG00000224078.13","gene_symbol":"SNHG14","gene_name":"small nucleolar RNA host gene 14 [Source:HGNC Symbol;Acc:HGNC:37462]","synonyms":"UBE3A-AS1,UBE3A-AS,NCRNA00214","biotype":"processed_transcript","ncbi_id":"104472715","summary":"This gene is located within the Prader-Willi critical region and produces a long, spliced paternally-imprinted RNA that initiates within a common upstream promoter region shared by the SNRPN (small nuclear ribonucleoprotein polypeptide N) and SNURF genes. This transcript serves as a host RNA for the small nucleolar RNA, C/D box 115 and 116 clusters. This RNA extends in antisense into the region of the ubiquitin protein ligase E3A gene (UBE3A), and is thought to regulate imprinted expression of UBE3A in the brain. This transcript undergoes extensive alternative splicing, and may initiate and terminate at multiple locations within this genomic region. The full-length structure of all splice forms is not determined. [provided by RefSeq, Mar 2017]","start":24978583,"end":25419462,"strand":1,"description":"small nucleolar RNA host gene 14 [Source:HGNC Symbol;Acc:HGNC:37462]"}, {"versioned_ensembl_gene_id":"ENSG00000163288.13","gene_symbol":"GABRB1","gene_name":"gamma-aminobutyric acid type A receptor beta1 subunit [Source:HGNC Symbol;Acc:HGNC:4081]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2560","summary":"The gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes GABA A receptor, beta 1 subunit. It is mapped to chromosome 4p12 in a cluster comprised of genes encoding alpha 4, alpha 2 and gamma 1 subunits of the GABA A receptor. Alteration of this gene is implicated in the pathogenetics of schizophrenia. [provided by RefSeq, Jul 2008]","start":46993723,"end":47426444,"strand":1,"description":"gamma-aminobutyric acid type A receptor beta1 subunit [Source:HGNC Symbol;Acc:HGNC:4081]"}, {"versioned_ensembl_gene_id":"ENSG00000226201.6","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32874193,"end":32878179,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000228826.2","gene_symbol":"AL592494.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121494379,"end":121510383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197386.10","gene_symbol":"HTT","gene_name":"huntingtin [Source:HGNC Symbol;Acc:HGNC:4851]","synonyms":"HD,IT15","biotype":"protein_coding","ncbi_id":"3064","summary":"Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5' UTR that inhibits expression of the huntingtin gene product through translational repression. [provided by RefSeq, Jul 2016]","start":3074681,"end":3243959,"strand":1,"description":"huntingtin [Source:HGNC Symbol;Acc:HGNC:4851]"}, {"versioned_ensembl_gene_id":"ENSG00000233432.2","gene_symbol":"AL592494.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121502344,"end":121503891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275857.1","gene_symbol":"AC009133.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29804430,"end":29804990,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273171.1","gene_symbol":"AC002094.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28364288,"end":28368012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277450.1","gene_symbol":"AC002094.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28373256,"end":28373562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103351.12","gene_symbol":"CLUAP1","gene_name":"clusterin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:19009]","synonyms":"KIAA0643,IFT38,FLJ13297,FAP22,CFAP22","biotype":"protein_coding","ncbi_id":"23059","summary":"The protein encoded by this gene contains a single coiled-coil region. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":3500924,"end":3539048,"strand":1,"description":"clusterin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:19009]"}, {"versioned_ensembl_gene_id":"ENSG00000236690.2","gene_symbol":"AC007274.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7690511,"end":7692678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206315.9","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"PBX2MHC,HOX12,G17","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32142341,"end":32147792,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000224493.1","gene_symbol":"AC093156.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75521562,"end":75522231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115255.10","gene_symbol":"REEP6","gene_name":"receptor accessory protein 6 [Source:HGNC Symbol;Acc:HGNC:30078]","synonyms":"DP1L1,C19orf32,Yip2f,FLJ25383","biotype":"protein_coding","ncbi_id":"92840","summary":"The protein encoded by this gene may be involved in the transport of receptors from the endoplasmic reticulum (ER) to the cell surface. The encoded protein may also play a role in regulating ER membrane structure. This gene is required for the proper development of retinal rods and photoreceptors, with defects in this gene being associated with retinitis pigmentosa 77. [provided by RefSeq, May 2017]","start":1490747,"end":1497927,"strand":1,"description":"receptor accessory protein 6 [Source:HGNC Symbol;Acc:HGNC:30078]"}, {"versioned_ensembl_gene_id":"ENSG00000234201.1","gene_symbol":"BMI1P1","gene_name":"BMI1 proto-oncogene, polycomb ring finger pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51428]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127902","summary":null,"start":67791955,"end":67792895,"strand":-1,"description":"BMI1 proto-oncogene, polycomb ring finger pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51428]"}, {"versioned_ensembl_gene_id":"ENSG00000233587.1","gene_symbol":"LINC01884","gene_name":"long intergenic non-protein coding RNA 1884 [Source:HGNC Symbol;Acc:HGNC:52703]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723362","summary":null,"start":22536479,"end":22538288,"strand":1,"description":"long intergenic non-protein coding RNA 1884 [Source:HGNC Symbol;Acc:HGNC:52703]"}, {"versioned_ensembl_gene_id":"ENSG00000225703.1","gene_symbol":"AC114737.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76972679,"end":76976961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157542.9","gene_symbol":"KCNJ6","gene_name":"potassium voltage-gated channel subfamily J member 6 [Source:HGNC Symbol;Acc:HGNC:6267]","synonyms":"BIR1,Kir3.2,KCNJ7,KATP2,hiGIRK2,GIRK2","biotype":"protein_coding","ncbi_id":"3763","summary":"This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]","start":37607376,"end":37916446,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 6 [Source:HGNC Symbol;Acc:HGNC:6267]"}, {"versioned_ensembl_gene_id":"ENSG00000224080.1","gene_symbol":"UBE2FP1","gene_name":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44535]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421436","summary":null,"start":37143512,"end":37143958,"strand":-1,"description":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44535]"}, {"versioned_ensembl_gene_id":"ENSG00000231686.1","gene_symbol":"Z97180.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146619597,"end":146620584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271425.7","gene_symbol":"NBPF10","gene_name":"NBPF member 10 [Source:HGNC Symbol;Acc:HGNC:31992]","synonyms":"AG1","biotype":"protein_coding","ncbi_id":"100132406","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":146064699,"end":146144804,"strand":-1,"description":"NBPF member 10 [Source:HGNC Symbol;Acc:HGNC:31992]"}, {"versioned_ensembl_gene_id":"ENSG00000259743.2","gene_symbol":"AC068714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46099193,"end":46100392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258808.1","gene_symbol":"LINC02310","gene_name":"long intergenic non-protein coding RNA 2310 [Source:HGNC Symbol;Acc:HGNC:53229]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370496","summary":null,"start":51392128,"end":51397135,"strand":-1,"description":"long intergenic non-protein coding RNA 2310 [Source:HGNC Symbol;Acc:HGNC:53229]"}, {"versioned_ensembl_gene_id":"ENSG00000095485.17","gene_symbol":"CWF19L1","gene_name":"CWF19 like 1, cell cycle control (S. pombe) [Source:HGNC Symbol;Acc:HGNC:25613]","synonyms":"hDrn1,FLJ10998","biotype":"protein_coding","ncbi_id":"55280","summary":"This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":100232298,"end":100267680,"strand":-1,"description":"CWF19 like 1, cell cycle control (S. pombe) [Source:HGNC Symbol;Acc:HGNC:25613]"}, {"versioned_ensembl_gene_id":"ENSG00000112031.15","gene_symbol":"MTRF1L","gene_name":"mitochondrial translational release factor 1 like [Source:HGNC Symbol;Acc:HGNC:21051]","synonyms":"mtRF1a,HMRF1L","biotype":"protein_coding","ncbi_id":"54516","summary":"The protein encoded by this gene plays a role in mitochondrial translation termination, and is thought to be a release factor that is involved in the dissociation of the complete protein from the final tRNA, the ribosome, and the cognate mRNA. This protein acts upon UAA and UAG stop codons, but has no in vitro activity against UGA, which encodes tryptophan in human mitochondrion, or, the mitochondrial non-cognate stop codons, AGA and AGG. This protein shares sequence similarity to bacterial release factors. Pseudogenes of this gene are found on chromosomes 4, 8, and 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":152987362,"end":153002685,"strand":-1,"description":"mitochondrial translational release factor 1 like [Source:HGNC Symbol;Acc:HGNC:21051]"}, {"versioned_ensembl_gene_id":"ENSG00000259200.1","gene_symbol":"AC068722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45705078,"end":45931069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231799.2","gene_symbol":"PA2G4P6","gene_name":"proliferation-associated 2G4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32219]","synonyms":"PA2G4L3","biotype":"processed_pseudogene","ncbi_id":"646083","summary":null,"start":89449558,"end":89450754,"strand":1,"description":"proliferation-associated 2G4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32219]"}, {"versioned_ensembl_gene_id":"ENSG00000225460.1","gene_symbol":"AL590233.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89472237,"end":89472692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182903.15","gene_symbol":"ZNF721","gene_name":"zinc finger protein 721 [Source:HGNC Symbol;Acc:HGNC:29425]","synonyms":"KIAA1982","biotype":"protein_coding","ncbi_id":"170960","summary":null,"start":425815,"end":499156,"strand":-1,"description":"zinc finger protein 721 [Source:HGNC Symbol;Acc:HGNC:29425]"}, {"versioned_ensembl_gene_id":"ENSG00000264343.5","gene_symbol":"NOTCH2NL","gene_name":"notch 2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:31862]","synonyms":"N2N","biotype":"protein_coding","ncbi_id":"388677","summary":null,"start":146146203,"end":146229026,"strand":-1,"description":"notch 2 N-terminal like [Source:HGNC Symbol;Acc:HGNC:31862]"}, {"versioned_ensembl_gene_id":"ENSG00000127588.4","gene_symbol":"GNG13","gene_name":"G protein subunit gamma 13 [Source:HGNC Symbol;Acc:HGNC:14131]","synonyms":"h2-35,G(gamma)13","biotype":"protein_coding","ncbi_id":"51764","summary":"Heterotrimeric G proteins, which consist of alpha (see MIM 139320), beta (see MIM 139380), and gamma subunits, function as signal transducers for the 7-transmembrane-helix G protein-coupled receptors. GNG13 is a gamma subunit that is expressed in taste, retinal, and neuronal tissues and plays a key role in taste transduction (Li et al., 2006 [PubMed 16473877]).[supplied by OMIM, Oct 2009]","start":798041,"end":800733,"strand":-1,"description":"G protein subunit gamma 13 [Source:HGNC Symbol;Acc:HGNC:14131]"}, {"versioned_ensembl_gene_id":"ENSG00000251595.7","gene_symbol":"ABCA11P","gene_name":"ATP binding cassette subfamily A member 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:31]","synonyms":"FLJ14297,EST1133530,ABCA11","biotype":"transcribed_processed_pseudogene","ncbi_id":"79963","summary":null,"start":425435,"end":474129,"strand":-1,"description":"ATP binding cassette subfamily A member 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:31]"}, {"versioned_ensembl_gene_id":"ENSG00000269946.1","gene_symbol":"AL158152.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94166289,"end":94200627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272885.1","gene_symbol":"AC092574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":416118,"end":416537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213240.8","gene_symbol":"AC239799.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":146113652,"end":146229000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269929.1","gene_symbol":"AL158152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94176458,"end":94177892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110321.16","gene_symbol":"EIF4G2","gene_name":"eukaryotic translation initiation factor 4 gamma 2 [Source:HGNC Symbol;Acc:HGNC:3297]","synonyms":"NAT1,DAP5,p97","biotype":"protein_coding","ncbi_id":"1982","summary":"Translation initiation is mediated by specific recognition of the cap structure by eukaryotic translation initiation factor 4F (eIF4F), which is a cap binding protein complex that consists of three subunits: eIF4A, eIF4E and eIF4G. The protein encoded by this gene shares similarity with the C-terminal region of eIF4G that contains the binding sites for eIF4A and eIF3; eIF4G, in addition, contains a binding site for eIF4E at the N-terminus. Unlike eIF4G, which supports cap-dependent and independent translation, this gene product functions as a general repressor of translation by forming translationally inactive complexes. In vitro and in vivo studies indicate that translation of this mRNA initiates exclusively at a non-AUG (GUG) codon. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]","start":10797050,"end":10809110,"strand":-1,"description":"eukaryotic translation initiation factor 4 gamma 2 [Source:HGNC Symbol;Acc:HGNC:3297]"}, {"versioned_ensembl_gene_id":"ENSG00000268181.3","gene_symbol":"AC073188.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63396341,"end":63399250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215343.7","gene_symbol":"ZNF705D","gene_name":"zinc finger protein 705D [Source:HGNC Symbol;Acc:HGNC:33202]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728957","summary":null,"start":12104389,"end":12115516,"strand":1,"description":"zinc finger protein 705D [Source:HGNC Symbol;Acc:HGNC:33202]"}, {"versioned_ensembl_gene_id":"ENSG00000214439.3","gene_symbol":"FAM185BP","gene_name":"family with sequence similarity 185 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:21813]","synonyms":"FAM185B","biotype":"unprocessed_pseudogene","ncbi_id":"641808","summary":null,"start":77083886,"end":77122116,"strand":-1,"description":"family with sequence similarity 185 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:21813]"}, {"versioned_ensembl_gene_id":"ENSG00000263196.1","gene_symbol":"MTND3P13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52073]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075277","summary":null,"start":10723424,"end":10723766,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:52073]"}, {"versioned_ensembl_gene_id":"ENSG00000228978.2","gene_symbol":"TNF","gene_name":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]","synonyms":"TNF-alpha,TNFSF2,DIF,TNFA","biotype":"protein_coding","ncbi_id":"7124","summary":"This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020]","start":31643520,"end":31645322,"strand":1,"description":"tumor necrosis factor [Source:HGNC Symbol;Acc:HGNC:11892]"}, {"versioned_ensembl_gene_id":"ENSG00000171497.4","gene_symbol":"PPID","gene_name":"peptidylprolyl isomerase D [Source:HGNC Symbol;Acc:HGNC:9257]","synonyms":"CYP-40","biotype":"protein_coding","ncbi_id":"5481","summary":"The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein has been shown to possess PPIase activity and, similar to other family members, can bind to the immunosuppressant cyclosporin A. [provided by RefSeq, Jul 2008]","start":158709134,"end":158723396,"strand":-1,"description":"peptidylprolyl isomerase D [Source:HGNC Symbol;Acc:HGNC:9257]"}, {"versioned_ensembl_gene_id":"ENSG00000089163.4","gene_symbol":"SIRT4","gene_name":"sirtuin 4 [Source:HGNC Symbol;Acc:HGNC:14932]","synonyms":"SIR2L4","biotype":"protein_coding","ncbi_id":"23409","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class IV of the sirtuin family. [provided by RefSeq, Jul 2008]","start":120302316,"end":120313249,"strand":1,"description":"sirtuin 4 [Source:HGNC Symbol;Acc:HGNC:14932]"}, {"versioned_ensembl_gene_id":"ENSG00000264339.1","gene_symbol":"AP001020.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":738058,"end":739444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175137.10","gene_symbol":"SH3BP5L","gene_name":"SH3 binding domain protein 5 like [Source:HGNC Symbol;Acc:HGNC:29360]","synonyms":"KIAA1720","biotype":"protein_coding","ncbi_id":"80851","summary":null,"start":248810446,"end":248826633,"strand":-1,"description":"SH3 binding domain protein 5 like [Source:HGNC Symbol;Acc:HGNC:29360]"}, {"versioned_ensembl_gene_id":"ENSG00000124882.3","gene_symbol":"EREG","gene_name":"epiregulin [Source:HGNC Symbol;Acc:HGNC:3443]","synonyms":"ER","biotype":"protein_coding","ncbi_id":"2069","summary":"This gene encodes a secreted peptide hormone and member of the epidermal growth factor (EGF) family of proteins. The encoded protein is a ligand of the epidermal growth factor receptor (EGFR) and the structurally related erb-b2 receptor tyrosine kinase 4 (ERBB4). The encoded protein may be involved in a wide range of biological processes including inflammation, wound healing, oocyte maturation, and cell proliferation. Additionally, the encoded protein may promote the progression of cancers of various human tissues. [provided by RefSeq, Jul 2015]","start":74365143,"end":74388751,"strand":1,"description":"epiregulin [Source:HGNC Symbol;Acc:HGNC:3443]"}, {"versioned_ensembl_gene_id":"ENSG00000267573.1","gene_symbol":"KRT8P5","gene_name":"keratin 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:31094]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"342732","summary":null,"start":44320800,"end":44322257,"strand":-1,"description":"keratin 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:31094]"}, {"versioned_ensembl_gene_id":"ENSG00000235343.1","gene_symbol":"LINC01665","gene_name":"long intergenic non-protein coding RNA 1665 [Source:HGNC Symbol;Acc:HGNC:52453]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929350","summary":null,"start":16746869,"end":16748645,"strand":-1,"description":"long intergenic non-protein coding RNA 1665 [Source:HGNC Symbol;Acc:HGNC:52453]"}, {"versioned_ensembl_gene_id":"ENSG00000171813.13","gene_symbol":"PWWP2B","gene_name":"PWWP domain containing 2B [Source:HGNC Symbol;Acc:HGNC:25150]","synonyms":"PWWP2,FLJ46823,bA432J24.1","biotype":"protein_coding","ncbi_id":"170394","summary":null,"start":132397168,"end":132417863,"strand":1,"description":"PWWP domain containing 2B [Source:HGNC Symbol;Acc:HGNC:25150]"}, {"versioned_ensembl_gene_id":"ENSG00000244720.1","gene_symbol":"AC055748.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111633672,"end":111635089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178904.18","gene_symbol":"DPY19L3","gene_name":"dpy-19 like 3 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:27120]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147991","summary":null,"start":32405543,"end":32485895,"strand":1,"description":"dpy-19 like 3 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:27120]"}, {"versioned_ensembl_gene_id":"ENSG00000269896.2","gene_symbol":"AL513477.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":2350414,"end":2352820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188610.12","gene_symbol":"FAM72B","gene_name":"family with sequence similarity 72 member B [Source:HGNC Symbol;Acc:HGNC:24805]","synonyms":"RP11-439A17.6","biotype":"protein_coding","ncbi_id":"653820","summary":null,"start":121167646,"end":121185539,"strand":-1,"description":"family with sequence similarity 72 member B [Source:HGNC Symbol;Acc:HGNC:24805]"}, {"versioned_ensembl_gene_id":"ENSG00000280138.1","gene_symbol":"AC027290.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":122870059,"end":122888720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119865.8","gene_symbol":"CNRIP1","gene_name":"cannabinoid receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24546]","synonyms":"DKFZP566K1924,CRIP1b,CRIP1a,CRIP1,C2orf32","biotype":"protein_coding","ncbi_id":"25927","summary":"This gene encodes a protein that interacts with the C-terminal tail of cannabinoid receptor 1. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013]","start":68284171,"end":68320051,"strand":-1,"description":"cannabinoid receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24546]"}, {"versioned_ensembl_gene_id":"ENSG00000232715.1","gene_symbol":"LINC01022","gene_name":"long intergenic non-protein coding RNA 1022 [Source:HGNC Symbol;Acc:HGNC:48998]","synonyms":"TCONS_00013107","biotype":"antisense_RNA","ncbi_id":"105375616","summary":null,"start":158590629,"end":158591120,"strand":1,"description":"long intergenic non-protein coding RNA 1022 [Source:HGNC Symbol;Acc:HGNC:48998]"}, {"versioned_ensembl_gene_id":"ENSG00000227718.1","gene_symbol":"AC016730.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13723048,"end":13758152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137975.7","gene_symbol":"CLCA2","gene_name":"chloride channel accessory 2 [Source:HGNC Symbol;Acc:HGNC:2016]","synonyms":"CLCRG2","biotype":"protein_coding","ncbi_id":"9635","summary":"This gene encodes a member of the calcium-activated chloride channel regulator (CLCR) family of proteins. Members of this family regulate the transport of chloride across the plasma membrane. The encoded protein is autoproteolytically processed to generate N- and C- terminal fragments. Expression of this gene is upregulated by the tumor suppressor protein p53 in response to DNA damage. In breast cancer, expression of this gene is downregulated and the encoded protein may inhibit migration and invasion while promoting mesenchymal-to-epithelial transition in cancer cell lines. [provided by RefSeq, Sep 2016]","start":86424086,"end":86456558,"strand":1,"description":"chloride channel accessory 2 [Source:HGNC Symbol;Acc:HGNC:2016]"}, {"versioned_ensembl_gene_id":"ENSG00000245293.2","gene_symbol":"AC096564.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107863479,"end":107978799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171612.6","gene_symbol":"SLC25A33","gene_name":"solute carrier family 25 member 33 [Source:HGNC Symbol;Acc:HGNC:29681]","synonyms":"PNC1,MGC4399,BMSC-MCP","biotype":"protein_coding","ncbi_id":"84275","summary":"SLC25A33 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":9539482,"end":9585179,"strand":1,"description":"solute carrier family 25 member 33 [Source:HGNC Symbol;Acc:HGNC:29681]"}, {"versioned_ensembl_gene_id":"ENSG00000206235.8","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"D6S217E,RING11,ABCB3,PSF2","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32975593,"end":32992541,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000234496.2","gene_symbol":"MRPS21P1","gene_name":"mitochondrial ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29748]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"199900","summary":null,"start":65092392,"end":65092614,"strand":-1,"description":"mitochondrial ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29748]"}, {"versioned_ensembl_gene_id":"ENSG00000235488.1","gene_symbol":"JARID2-AS1","gene_name":"JARID2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40314]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506681","summary":null,"start":15247815,"end":15248634,"strand":-1,"description":"JARID2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40314]"}, {"versioned_ensembl_gene_id":"ENSG00000230519.2","gene_symbol":"HMGB1P49","gene_name":"high mobility group box 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:39282]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420013","summary":null,"start":27702338,"end":27702906,"strand":1,"description":"high mobility group box 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:39282]"}, {"versioned_ensembl_gene_id":"ENSG00000206320.12","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32138576,"end":32141932,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000134690.10","gene_symbol":"CDCA8","gene_name":"cell division cycle associated 8 [Source:HGNC Symbol;Acc:HGNC:14629]","synonyms":"MESRGP,FLJ12042,DasraB,BOR","biotype":"protein_coding","ncbi_id":"55143","summary":"This gene encodes a component of the chromosomal passenger complex. This complex is an essential regulator of mitosis and cell division. This protein is cell-cycle regulated and is required for chromatin-induced microtubule stabilization and spindle formation. Alternate splicing results in multiple transcript variants. Pseudgenes of this gene are found on chromosomes 7, 8 and 16. [provided by RefSeq, Apr 2013]","start":37692418,"end":37709719,"strand":1,"description":"cell division cycle associated 8 [Source:HGNC Symbol;Acc:HGNC:14629]"}, {"versioned_ensembl_gene_id":"ENSG00000271888.1","gene_symbol":"AL136162.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15243923,"end":15245000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234044.1","gene_symbol":"AC108059.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128067194,"end":128067407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106853.18","gene_symbol":"PTGR1","gene_name":"prostaglandin reductase 1 [Source:HGNC Symbol;Acc:HGNC:18429]","synonyms":"ZADH3,LTB4DH","biotype":"protein_coding","ncbi_id":"22949","summary":"This gene encodes an enzyme that is involved in the inactivation of the chemotactic factor, leukotriene B4. The encoded protein specifically catalyzes the NADP+ dependent conversion of leukotriene B4 to 12-oxo-leukotriene B4. A pseudogene of this gene is found on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":111549722,"end":111599855,"strand":-1,"description":"prostaglandin reductase 1 [Source:HGNC Symbol;Acc:HGNC:18429]"}, {"versioned_ensembl_gene_id":"ENSG00000251501.1","gene_symbol":"AC114774.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43586328,"end":43588097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274148.5","gene_symbol":"LILRA6","gene_name":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]","synonyms":"CD85b,LILRB6,ILT8","biotype":"protein_coding","ncbi_id":"79168","summary":null,"start":54237215,"end":54243458,"strand":-1,"description":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]"}, {"versioned_ensembl_gene_id":"ENSG00000171487.14","gene_symbol":"NLRP5","gene_name":"NLR family pyrin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21269]","synonyms":"PYPAF8,PAN11,NALP5,MATER,CLR19.8","biotype":"protein_coding","ncbi_id":"126206","summary":"The protein encoded by this gene belongs to the NALP protein family. Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). Expression of this gene is restricted to the oocyte. A mouse gene that encodes a maternal oocyte protein, similar to this encoded protein, is required for normal early embryogenesis. [provided by RefSeq, Jul 2008]","start":55999726,"end":56061813,"strand":1,"description":"NLR family pyrin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21269]"}, {"versioned_ensembl_gene_id":"ENSG00000152214.12","gene_symbol":"RIT2","gene_name":"Ras like without CAAX 2 [Source:HGNC Symbol;Acc:HGNC:10017]","synonyms":"RIN,RIBA","biotype":"protein_coding","ncbi_id":"6014","summary":"RIN belongs to the RAS (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]","start":42743227,"end":43115691,"strand":-1,"description":"Ras like without CAAX 2 [Source:HGNC Symbol;Acc:HGNC:10017]"}, {"versioned_ensembl_gene_id":"ENSG00000224717.1","gene_symbol":"AC098936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":205455929,"end":205469024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152591.12","gene_symbol":"DSPP","gene_name":"dentin sialophosphoprotein [Source:HGNC Symbol;Acc:HGNC:3054]","synonyms":"DFNA39,DMP3,DGI1","biotype":"protein_coding","ncbi_id":"1834","summary":"This gene encodes a member of the small integrin-binding ligand N-linked glycoprotein (SIBLING) family of proteins. The encoded preproprotein is secreted by odontoblasts and proteolytically processed to generate two principal proteins of the dentin extracellular matrix of the tooth, dentin sialoprotein and dentin phosphoprotein. These two protein products may play distinct but related roles in dentin mineralization. Mutations in this gene are associated with dentinogenesis imperfecta and dentin dysplasia. This gene is present in a gene cluster on chromosome 4. Allelic differences due to repeat polymorphisms have been found for this gene. [provided by RefSeq, Jan 2016]","start":87608529,"end":87616910,"strand":1,"description":"dentin sialophosphoprotein [Source:HGNC Symbol;Acc:HGNC:3054]"}, {"versioned_ensembl_gene_id":"ENSG00000183844.16","gene_symbol":"FAM3B","gene_name":"family with sequence similarity 3 member B [Source:HGNC Symbol;Acc:HGNC:1253]","synonyms":"PRED44,PANDER,ORF9,D21M16SJHU19e,C21orf76,C21orf11,2-21","biotype":"protein_coding","ncbi_id":"54097","summary":null,"start":41304212,"end":41357431,"strand":1,"description":"family with sequence similarity 3 member B [Source:HGNC Symbol;Acc:HGNC:1253]"}, {"versioned_ensembl_gene_id":"ENSG00000177201.2","gene_symbol":"OR2T12","gene_name":"olfactory receptor family 2 subfamily T member 12 [Source:HGNC Symbol;Acc:HGNC:19592]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127064","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248290139,"end":248303424,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 12 [Source:HGNC Symbol;Acc:HGNC:19592]"}, {"versioned_ensembl_gene_id":"ENSG00000183574.12","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"RMA1,NG2,G16,RING5","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32135962,"end":32138401,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000006712.14","gene_symbol":"PAF1","gene_name":"PAF1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:25459]","synonyms":"PD2,FLJ11123,F23149_1","biotype":"protein_coding","ncbi_id":"54623","summary":"This gene encodes a subunit of the polymerase associated factor (PAF1) complex. The PAF1 complex interacts with RNA polymerase II and plays a role in transcription elongation as well as histone modifications including ubiquitylation and methylation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":39385852,"end":39391195,"strand":-1,"description":"PAF1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:25459]"}, {"versioned_ensembl_gene_id":"ENSG00000250892.1","gene_symbol":"AC108475.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":201409,"end":205009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270723.1","gene_symbol":"RPL23AP92","gene_name":"ribosomal protein L23a pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:51627]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481731","summary":null,"start":69873565,"end":69873819,"strand":-1,"description":"ribosomal protein L23a pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:51627]"}, {"versioned_ensembl_gene_id":"ENSG00000255205.1","gene_symbol":"MED28P5","gene_name":"mediator complex subunit 28 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45082]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479053","summary":null,"start":97000274,"end":97000711,"strand":-1,"description":"mediator complex subunit 28 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45082]"}, {"versioned_ensembl_gene_id":"ENSG00000254587.1","gene_symbol":"AP003066.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96590317,"end":96713822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254872.3","gene_symbol":"AC139749.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1049880,"end":1055749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231567.1","gene_symbol":"MTND2P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42120]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873225","summary":null,"start":140217651,"end":140220368,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42120]"}, {"versioned_ensembl_gene_id":"ENSG00000257751.2","gene_symbol":"AL512310.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19668542,"end":19669056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118407.14","gene_symbol":"FILIP1","gene_name":"filamin A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21015]","synonyms":"FILIP,KIAA1275","biotype":"protein_coding","ncbi_id":"27145","summary":"This gene encodes a filamin A binding protein. The encoded protein promotes the degradation of filamin A and may regulate cortical neuron migration and dendritic spine morphology. Mice lacking a functional copy of this gene exhibit reduced dendritic spine length and altered excitatory signaling. [provided by RefSeq, Oct 2016]","start":75291859,"end":75493738,"strand":-1,"description":"filamin A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21015]"}, {"versioned_ensembl_gene_id":"ENSG00000248128.1","gene_symbol":"AC114801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78003143,"end":78003439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282123.1","gene_symbol":"IGHV7-34-1","gene_name":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28382","summary":null,"start":106401981,"end":106402414,"strand":-1,"description":"immunoglobulin heavy variable 7-34-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5664]"}, {"versioned_ensembl_gene_id":"ENSG00000230305.2","gene_symbol":"AC004980.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":76524515,"end":76532692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258573.5","gene_symbol":"AL163195.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20587644,"end":20607137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243945.1","gene_symbol":"AC078918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109977540,"end":109977767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241360.1","gene_symbol":"PDXP","gene_name":"pyridoxal phosphatase [Source:HGNC Symbol;Acc:HGNC:30259]","synonyms":"FLJ32703,dJ37E16.5,CIN","biotype":"protein_coding","ncbi_id":"57026","summary":"Pyridoxal 5-prime-phosphate (PLP) is the active form of vitamin B6 that acts as a coenzyme in maintaining biochemical homeostasis. The preferred degradation route from PLP to 4-pyridoxic acid involves the dephosphorylation of PLP by PDXP (Jang et al., 2003 [PubMed 14522954]).[supplied by OMIM, Mar 2008]","start":37658727,"end":37666934,"strand":1,"description":"pyridoxal phosphatase [Source:HGNC Symbol;Acc:HGNC:30259]"}, {"versioned_ensembl_gene_id":"ENSG00000227367.1","gene_symbol":"SLC9B1P4","gene_name":"solute carrier family 9 member B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43583]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644768","summary":null,"start":16428947,"end":16476870,"strand":-1,"description":"solute carrier family 9 member B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43583]"}, {"versioned_ensembl_gene_id":"ENSG00000276822.1","gene_symbol":"AC009053.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":74393076,"end":74393183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233415.1","gene_symbol":"AL133419.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40031585,"end":40043889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230294.4","gene_symbol":"LINC02370","gene_name":"long intergenic non-protein coding RNA 2370 [Source:HGNC Symbol;Acc:HGNC:27885]","synonyms":null,"biotype":"lincRNA","ncbi_id":"338797","summary":null,"start":131347470,"end":131367555,"strand":1,"description":"long intergenic non-protein coding RNA 2370 [Source:HGNC Symbol;Acc:HGNC:27885]"}, {"versioned_ensembl_gene_id":"ENSG00000196436.8","gene_symbol":"NPIPB15","gene_name":"nuclear pore complex interacting protein family member B15 [Source:HGNC Symbol;Acc:HGNC:34409]","synonyms":"NPIPL2,LOC440348","biotype":"protein_coding","ncbi_id":"440348","summary":null,"start":74377878,"end":74392080,"strand":1,"description":"nuclear pore complex interacting protein family member B15 [Source:HGNC Symbol;Acc:HGNC:34409]"}, {"versioned_ensembl_gene_id":"ENSG00000119185.12","gene_symbol":"ITGB1BP1","gene_name":"integrin subunit beta 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23927]","synonyms":"ICAP-1B,ICAP-1alpha,ICAP-1A,ICAP1B,ICAP1A,ICAP1","biotype":"protein_coding","ncbi_id":"9270","summary":"The cytoplasmic domains of integrins are essential for cell adhesion. The protein encoded by this gene binds to the beta1 integrin cytoplasmic domain. The interaction between this protein and beta1 integrin is highly specific. Two isoforms of this protein are derived from alternatively spliced transcripts. The shorter form of this protein does not interact with the beta1 integrin cytoplasmic domain. The longer form is a phosphoprotein and the extent of its phosphorylation is regulated by the cell-matrix interaction, suggesting an important role of this protein during integrin-dependent cell adhesion. Several transcript variants, some protein-coding and some non-protein coding, have been found for this gene. [provided by RefSeq, Jan 2016]","start":9403475,"end":9423547,"strand":-1,"description":"integrin subunit beta 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:23927]"}, {"versioned_ensembl_gene_id":"ENSG00000139055.6","gene_symbol":"ERP27","gene_name":"endoplasmic reticulum protein 27 [Source:HGNC Symbol;Acc:HGNC:26495]","synonyms":"PDIA8,FLJ32115,ERp27,C12orf46","biotype":"protein_coding","ncbi_id":"121506","summary":"This gene encodes a noncatalytic member of the protein disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins. The canonical protein has an N-terminal signal sequence, two thioredoxin (TRX)-like domains and a C-terminal ER-retention sequence. Alternative splicing results in multiple transcript variants encoding distinct isoforms; some of which lack domains present in the canonical protein. [provided by RefSeq, Dec 2016]","start":14914035,"end":14939082,"strand":-1,"description":"endoplasmic reticulum protein 27 [Source:HGNC Symbol;Acc:HGNC:26495]"}, {"versioned_ensembl_gene_id":"ENSG00000234450.1","gene_symbol":"AC005534.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156633355,"end":156633787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224903.1","gene_symbol":"AC005534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156654185,"end":156657693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278957.1","gene_symbol":"AC012354.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44927914,"end":44928396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259439.2","gene_symbol":"LINC01833","gene_name":"long intergenic non-protein coding RNA 1833 [Source:HGNC Symbol;Acc:HGNC:52644]","synonyms":"RP11-89,K21.1","biotype":"lincRNA","ncbi_id":"107985879","summary":null,"start":44921077,"end":44939199,"strand":-1,"description":"long intergenic non-protein coding RNA 1833 [Source:HGNC Symbol;Acc:HGNC:52644]"}, {"versioned_ensembl_gene_id":"ENSG00000188655.10","gene_symbol":"RNASE9","gene_name":"ribonuclease A family member 9 (inactive) [Source:HGNC Symbol;Acc:HGNC:20673]","synonyms":"RAK1,h461","biotype":"protein_coding","ncbi_id":"390443","summary":null,"start":20556093,"end":20560931,"strand":-1,"description":"ribonuclease A family member 9 (inactive) [Source:HGNC Symbol;Acc:HGNC:20673]"}, {"versioned_ensembl_gene_id":"ENSG00000224164.1","gene_symbol":"AL133264.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24742302,"end":24751921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259636.1","gene_symbol":"AC016987.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":86932880,"end":86946331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272602.5","gene_symbol":"ZNF595","gene_name":"zinc finger protein 595 [Source:HGNC Symbol;Acc:HGNC:27196]","synonyms":"FLJ31740","biotype":"protein_coding","ncbi_id":"152687","summary":"This gene encodes a protein belonging to the Cys2His2 zinc finger protein family, whose members function as transcription factors that can regulate a broad variety of developmental and cellular processes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Oct 2013]","start":53285,"end":88211,"strand":1,"description":"zinc finger protein 595 [Source:HGNC Symbol;Acc:HGNC:27196]"}, {"versioned_ensembl_gene_id":"ENSG00000248926.1","gene_symbol":"AC114801.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77958000,"end":77958780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184956.15","gene_symbol":"MUC6","gene_name":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4588","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. [provided by RefSeq, Dec 2016]","start":1012821,"end":1036706,"strand":-1,"description":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]"}, {"versioned_ensembl_gene_id":"ENSG00000257253.2","gene_symbol":"AC131157.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49861207,"end":49865802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163939.18","gene_symbol":"PBRM1","gene_name":"polybromo 1 [Source:HGNC Symbol;Acc:HGNC:30064]","synonyms":"PB1,BAF180","biotype":"protein_coding","ncbi_id":"55193","summary":"This locus encodes a subunit of ATP-dependent chromatin-remodeling complexes. The encoded protein has been identified as in integral component of complexes necessary for ligand-dependent transcriptional activation by nuclear hormone receptors. Mutations at this locus have been associated with primary clear cell renal cell carcinoma. [provided by RefSeq, Feb 2012]","start":52545352,"end":52685917,"strand":-1,"description":"polybromo 1 [Source:HGNC Symbol;Acc:HGNC:30064]"}, {"versioned_ensembl_gene_id":"ENSG00000105610.4","gene_symbol":"KLF1","gene_name":"Kruppel like factor 1 [Source:HGNC Symbol;Acc:HGNC:6345]","synonyms":"EKLF","biotype":"protein_coding","ncbi_id":"10661","summary":"This gene encodes a hematopoietic-specific transcription factor that induces high-level expression of adult beta-globin and other erythroid genes. The zinc-finger protein binds to the DNA sequence CCACACCCT found in the beta hemoglobin promoter. Heterozygous loss-of-function mutations in this gene result in the dominant In(Lu) blood phenotype. [provided by RefSeq, Oct 2009]","start":12884423,"end":12887181,"strand":-1,"description":"Kruppel like factor 1 [Source:HGNC Symbol;Acc:HGNC:6345]"}, {"versioned_ensembl_gene_id":"ENSG00000104723.20","gene_symbol":"TUSC3","gene_name":"tumor suppressor candidate 3 [Source:HGNC Symbol;Acc:HGNC:30242]","synonyms":"OST3A,N33,MRT7,MGC13453","biotype":"protein_coding","ncbi_id":"7991","summary":"This gene encodes a protein that has been associated with several biological functions including cellular magnesium uptake, protein glycosylation and embryonic development. This protein localizes to the endoplasmic reticulum and acts as a component of the oligosaccharyl transferase complex which is responsible for N-linked protein glycosylation. This gene is a candidate tumor suppressor gene. Homozygous mutations in this gene are associated with autosomal recessive nonsyndromic mental retardation-7 and in the proliferation and invasiveness of several cancers including metastatic pancreatic cancer, ovarian cancer and glioblastoma multiform. [provided by RefSeq, Oct 2017]","start":15417215,"end":15766649,"strand":1,"description":"tumor suppressor candidate 3 [Source:HGNC Symbol;Acc:HGNC:30242]"}, {"versioned_ensembl_gene_id":"ENSG00000203402.2","gene_symbol":"AL591503.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47297852,"end":47298721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135248.15","gene_symbol":"FAM71F1","gene_name":"family with sequence similarity 71 member F1 [Source:HGNC Symbol;Acc:HGNC:30704]","synonyms":"NYD-SP18,FAM137A","biotype":"protein_coding","ncbi_id":"84691","summary":null,"start":128709061,"end":128731743,"strand":1,"description":"family with sequence similarity 71 member F1 [Source:HGNC Symbol;Acc:HGNC:30704]"}, {"versioned_ensembl_gene_id":"ENSG00000283765.1","gene_symbol":"AC131160.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":183815568,"end":183884889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147117.7","gene_symbol":"ZNF157","gene_name":"zinc finger protein 157 [Source:HGNC Symbol;Acc:HGNC:12942]","synonyms":"HZF22","biotype":"protein_coding","ncbi_id":"7712","summary":"This gene product is a likely zinc finger family transcription factor. It contains KRAB-A and KRAB-B domains that act as transcriptional repressors in related proteins, and multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. This gene is part of a gene cluster on chromosome Xp11.23. [provided by RefSeq, Jul 2008]","start":47370583,"end":47414305,"strand":1,"description":"zinc finger protein 157 [Source:HGNC Symbol;Acc:HGNC:12942]"}, {"versioned_ensembl_gene_id":"ENSG00000205593.11","gene_symbol":"DENND6B","gene_name":"DENN domain containing 6B [Source:HGNC Symbol;Acc:HGNC:32690]","synonyms":"MGC33692,FAM116B,AFI1B","biotype":"protein_coding","ncbi_id":"414918","summary":null,"start":50309030,"end":50327060,"strand":-1,"description":"DENN domain containing 6B [Source:HGNC Symbol;Acc:HGNC:32690]"}, {"versioned_ensembl_gene_id":"ENSG00000260068.1","gene_symbol":"AC009101.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64738323,"end":64738564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242041.1","gene_symbol":"RPL35AP28","gene_name":"ribosomal protein L35a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36480]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271637","summary":null,"start":49863173,"end":49863503,"strand":1,"description":"ribosomal protein L35a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36480]"}, {"versioned_ensembl_gene_id":"ENSG00000164488.11","gene_symbol":"DACT2","gene_name":"dishevelled binding antagonist of beta catenin 2 [Source:HGNC Symbol;Acc:HGNC:21231]","synonyms":"C6orf116,bA503C24.7,DAPPER2","biotype":"protein_coding","ncbi_id":"168002","summary":null,"start":168292830,"end":168319754,"strand":-1,"description":"dishevelled binding antagonist of beta catenin 2 [Source:HGNC Symbol;Acc:HGNC:21231]"}, {"versioned_ensembl_gene_id":"ENSG00000283422.1","gene_symbol":"LINC02452","gene_name":"long intergenic non-protein coding RNA 2452 [Source:HGNC Symbol;Acc:HGNC:53384]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369924","summary":null,"start":96160692,"end":96172126,"strand":-1,"description":"long intergenic non-protein coding RNA 2452 [Source:HGNC Symbol;Acc:HGNC:53384]"}, {"versioned_ensembl_gene_id":"ENSG00000115419.12","gene_symbol":"GLS","gene_name":"glutaminase [Source:HGNC Symbol;Acc:HGNC:4331]","synonyms":"KIAA0838,GLS1","biotype":"protein_coding","ncbi_id":"2744","summary":"This gene encodes the K-type mitochondrial glutaminase. The encoded protein is an phosphate-activated amidohydrolase that catalyzes the hydrolysis of glutamine to glutamate and ammonia. This protein is primarily expressed in the brain and kidney plays an essential role in generating energy for metabolism, synthesizing the brain neurotransmitter glutamate and maintaining acid-base balance in the kidney. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":190880827,"end":190965552,"strand":1,"description":"glutaminase [Source:HGNC Symbol;Acc:HGNC:4331]"}, {"versioned_ensembl_gene_id":"ENSG00000254239.1","gene_symbol":"AC002428.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135897637,"end":135900250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237844.1","gene_symbol":"AC016766.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163749573,"end":164352223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229641.1","gene_symbol":"CYP2C56P","gene_name":"cytochrome P450 family 2 subfamily C member 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:39971]","synonyms":"CYP2C-se1[7]","biotype":"processed_pseudogene","ncbi_id":"106478959","summary":null,"start":164321933,"end":164322223,"strand":1,"description":"cytochrome P450 family 2 subfamily C member 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:39971]"}, {"versioned_ensembl_gene_id":"ENSG00000274657.2","gene_symbol":"LINC01658","gene_name":"long intergenic non-protein coding RNA 1658 [Source:HGNC Symbol;Acc:HGNC:52446]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388882","summary":null,"start":23462086,"end":23486981,"strand":-1,"description":"long intergenic non-protein coding RNA 1658 [Source:HGNC Symbol;Acc:HGNC:52446]"}, {"versioned_ensembl_gene_id":"ENSG00000249306.5","gene_symbol":"LINC01411","gene_name":"long intergenic non-protein coding RNA 1411 [Source:HGNC Symbol;Acc:HGNC:50703]","synonyms":"RP11-267A15.1","biotype":"lincRNA","ncbi_id":"101928176","summary":null,"start":174336295,"end":174532457,"strand":1,"description":"long intergenic non-protein coding RNA 1411 [Source:HGNC Symbol;Acc:HGNC:50703]"}, {"versioned_ensembl_gene_id":"ENSG00000249584.1","gene_symbol":"LINC02225","gene_name":"long intergenic non-protein coding RNA 2225 [Source:HGNC Symbol;Acc:HGNC:53094]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928539","summary":null,"start":57890327,"end":57899162,"strand":-1,"description":"long intergenic non-protein coding RNA 2225 [Source:HGNC Symbol;Acc:HGNC:53094]"}, {"versioned_ensembl_gene_id":"ENSG00000179846.9","gene_symbol":"NKPD1","gene_name":"NTPase KAP family P-loop domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24739]","synonyms":"FLJ33600","biotype":"protein_coding","ncbi_id":"284353","summary":null,"start":45149750,"end":45158737,"strand":-1,"description":"NTPase KAP family P-loop domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24739]"}, {"versioned_ensembl_gene_id":"ENSG00000256077.5","gene_symbol":"LINC02442","gene_name":"long intergenic non-protein coding RNA 2442 [Source:HGNC Symbol;Acc:HGNC:53374]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369815","summary":null,"start":67571197,"end":67589987,"strand":-1,"description":"long intergenic non-protein coding RNA 2442 [Source:HGNC Symbol;Acc:HGNC:53374]"}, {"versioned_ensembl_gene_id":"ENSG00000116001.15","gene_symbol":"TIA1","gene_name":"TIA1 cytotoxic granule associated RNA binding protein [Source:HGNC Symbol;Acc:HGNC:11802]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7072","summary":"The product encoded by this gene is a member of a RNA-binding protein family and possesses nucleolytic activity against cytotoxic lymphocyte (CTL) target cells. It has been suggested that this protein may be involved in the induction of apoptosis as it preferentially recognizes poly(A) homopolymers and induces DNA fragmentation in CTL targets. The major granule-associated species is a 15-kDa protein that is thought to be derived from the carboxyl terminus of the 40-kDa product by proteolytic processing. Alternative splicing resulting in different isoforms has been found for this gene. [provided by RefSeq, May 2017]","start":70209444,"end":70248660,"strand":-1,"description":"TIA1 cytotoxic granule associated RNA binding protein [Source:HGNC Symbol;Acc:HGNC:11802]"}, {"versioned_ensembl_gene_id":"ENSG00000160310.17","gene_symbol":"PRMT2","gene_name":"protein arginine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:5186]","synonyms":"MGC111373,HRMT1L1","biotype":"protein_coding","ncbi_id":"3275","summary":null,"start":46635167,"end":46665124,"strand":1,"description":"protein arginine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:5186]"}, {"versioned_ensembl_gene_id":"ENSG00000130055.13","gene_symbol":"GDPD2","gene_name":"glycerophosphodiester phosphodiesterase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25974]","synonyms":"OBDPF,GDE3,FLJ20207","biotype":"protein_coding","ncbi_id":"54857","summary":"This gene encodes a member of the glycerophosphodiester phosphodiesterase enzyme family. The encoded protein hydrolyzes glycerophosphoinositol to produce inositol 1-phosphate and glycerol. This protein may have a role in osteoblast differentiation and growth. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010]","start":70423031,"end":70433390,"strand":1,"description":"glycerophosphodiester phosphodiesterase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25974]"}, {"versioned_ensembl_gene_id":"ENSG00000284391.1","gene_symbol":"AL139398.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70427450,"end":70435350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160882.11","gene_symbol":"CYP11B1","gene_name":"cytochrome P450 family 11 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2591]","synonyms":"P450C11,FHI,CYP11B,CPN1","biotype":"protein_coding","ncbi_id":"1584","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane and is involved in the conversion of progesterone to cortisol in the adrenal cortex. Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency. Transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]","start":142872356,"end":142879846,"strand":-1,"description":"cytochrome P450 family 11 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2591]"}, {"versioned_ensembl_gene_id":"ENSG00000251380.3","gene_symbol":"DCANP1","gene_name":"dendritic cell associated nuclear protein [Source:HGNC Symbol;Acc:HGNC:24459]","synonyms":"DCNP1,C5orf20","biotype":"protein_coding","ncbi_id":"140947","summary":"This intronless gene is specifically expressed in dendritic cells (DCs), which are potent antigen-presenting cells involved in activating naive T cells to initiate antigen-specific immune response. The encoded protein is localized mainly in the perinucleus. One of the alleles (A/T) of this gene, that causes premature translation termination at aa 117, has been associated with an increased prevalence of major depression in humans. [provided by RefSeq, Jul 2008]","start":135444214,"end":135447348,"strand":-1,"description":"dendritic cell associated nuclear protein [Source:HGNC Symbol;Acc:HGNC:24459]"}, {"versioned_ensembl_gene_id":"ENSG00000153303.16","gene_symbol":"FRMD1","gene_name":"FERM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21240]","synonyms":"FLJ40260,FLJ22615,FLJ00181,DKFZp434O0117,bA164L23.1","biotype":"protein_coding","ncbi_id":"79981","summary":null,"start":168055745,"end":168081557,"strand":-1,"description":"FERM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21240]"}, {"versioned_ensembl_gene_id":"ENSG00000273424.1","gene_symbol":"AL008582.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41430934,"end":41431375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172264.16","gene_symbol":"MACROD2","gene_name":"MACRO domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16126]","synonyms":"dJ631M13.5,C20orf133","biotype":"protein_coding","ncbi_id":"140733","summary":"The protein encoded by this gene is a deacetylase involved in removing ADP-ribose from mono-ADP-ribosylated proteins. The encoded protein has been shown to translocate from the nucleus to the cytoplasm upon DNA damage. [provided by RefSeq, May 2017]","start":13995369,"end":16053197,"strand":1,"description":"MACRO domain containing 2 [Source:HGNC Symbol;Acc:HGNC:16126]"}, {"versioned_ensembl_gene_id":"ENSG00000213950.2","gene_symbol":"RPS10P2","gene_name":"ribosomal protein S10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16594]","synonyms":"dJ858M22.1","biotype":"processed_pseudogene","ncbi_id":"140758","summary":null,"start":14757563,"end":14758056,"strand":1,"description":"ribosomal protein S10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16594]"}, {"versioned_ensembl_gene_id":"ENSG00000121900.18","gene_symbol":"TMEM54","gene_name":"transmembrane protein 54 [Source:HGNC Symbol;Acc:HGNC:24143]","synonyms":"CAC-1","biotype":"protein_coding","ncbi_id":"113452","summary":null,"start":32894594,"end":32901438,"strand":-1,"description":"transmembrane protein 54 [Source:HGNC Symbol;Acc:HGNC:24143]"}, {"versioned_ensembl_gene_id":"ENSG00000214194.8","gene_symbol":"SMIM30","gene_name":"small integral membrane protein 30 [Source:HGNC Symbol;Acc:HGNC:48953]","synonyms":"LINC00998","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":113116718,"end":113118613,"strand":-1,"description":"small integral membrane protein 30 [Source:HGNC Symbol;Acc:HGNC:48953]"}, {"versioned_ensembl_gene_id":"ENSG00000273982.1","gene_symbol":"AC005746.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61354763,"end":61355155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267449.1","gene_symbol":"AC005884.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61069856,"end":61070356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237832.1","gene_symbol":"AL138808.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14933843,"end":14935363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153790.11","gene_symbol":"C7orf31","gene_name":"chromosome 7 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:21722]","synonyms":null,"biotype":"protein_coding","ncbi_id":"136895","summary":null,"start":25134697,"end":25180356,"strand":-1,"description":"chromosome 7 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:21722]"}, {"versioned_ensembl_gene_id":"ENSG00000237506.3","gene_symbol":"RPSAP15","gene_name":"ribosomal protein SA pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:31464]","synonyms":"LAMRL5,LAMR1P15","biotype":"processed_pseudogene","ncbi_id":"220885","summary":null,"start":87703343,"end":87704203,"strand":-1,"description":"ribosomal protein SA pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:31464]"}, {"versioned_ensembl_gene_id":"ENSG00000232756.1","gene_symbol":"AC004990.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77990384,"end":77995171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105290.11","gene_symbol":"APLP1","gene_name":"amyloid beta precursor like protein 1 [Source:HGNC Symbol;Acc:HGNC:597]","synonyms":"APLP","biotype":"protein_coding","ncbi_id":"333","summary":"This gene encodes a member of the highly conserved amyloid precursor protein gene family. The encoded protein is a membrane-associated glycoprotein that is cleaved by secretases in a manner similar to amyloid beta A4 precursor protein cleavage. This cleavage liberates an intracellular cytoplasmic fragment that may act as a transcriptional activator. The encoded protein may also play a role in synaptic maturation during cortical development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":35867899,"end":35879791,"strand":1,"description":"amyloid beta precursor like protein 1 [Source:HGNC Symbol;Acc:HGNC:597]"}, {"versioned_ensembl_gene_id":"ENSG00000259083.1","gene_symbol":"AL132639.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39174885,"end":39175880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270354.1","gene_symbol":"AC012368.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64208498,"end":64208716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260350.1","gene_symbol":"AC012173.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8847650,"end":8848724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266943.1","gene_symbol":"RPSAP66","gene_name":"ribosomal protein SA pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:51916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075110","summary":null,"start":60564740,"end":60565671,"strand":-1,"description":"ribosomal protein SA pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:51916]"}, {"versioned_ensembl_gene_id":"ENSG00000182841.12","gene_symbol":"RRP7BP","gene_name":"ribosomal RNA processing 7 homolog B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30454]","synonyms":"RRP7B,dJ222E13.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"91695","summary":null,"start":42555223,"end":42582038,"strand":-1,"description":"ribosomal RNA processing 7 homolog B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30454]"}, {"versioned_ensembl_gene_id":"ENSG00000196224.7","gene_symbol":"KRTAP5-3","gene_name":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]","synonyms":"KRTAP5.3,KRTAP5-9","biotype":"protein_coding","ncbi_id":"387266","summary":null,"start":1607565,"end":1608463,"strand":-1,"description":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]"}, {"versioned_ensembl_gene_id":"ENSG00000268951.1","gene_symbol":"AL772155.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63719864,"end":63720441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145242.13","gene_symbol":"EPHA5","gene_name":"EPH receptor A5 [Source:HGNC Symbol;Acc:HGNC:3389]","synonyms":"TYRO4,Hek7,EHK1,CEK7","biotype":"protein_coding","ncbi_id":"2044","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Aug 2013]","start":65319563,"end":65670495,"strand":-1,"description":"EPH receptor A5 [Source:HGNC Symbol;Acc:HGNC:3389]"}, {"versioned_ensembl_gene_id":"ENSG00000178338.10","gene_symbol":"ZNF354B","gene_name":"zinc finger protein 354B [Source:HGNC Symbol;Acc:HGNC:17197]","synonyms":"KID2,FLJ25008","biotype":"protein_coding","ncbi_id":"117608","summary":null,"start":178859953,"end":178888122,"strand":1,"description":"zinc finger protein 354B [Source:HGNC Symbol;Acc:HGNC:17197]"}, {"versioned_ensembl_gene_id":"ENSG00000259349.1","gene_symbol":"AC011921.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60526293,"end":60550798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276430.2","gene_symbol":"FAM25C","gene_name":"family with sequence similarity 25 member C [Source:HGNC Symbol;Acc:HGNC:23586]","synonyms":"bA164N7.4","biotype":"protein_coding","ncbi_id":"644054","summary":null,"start":47995355,"end":47999791,"strand":-1,"description":"family with sequence similarity 25 member C [Source:HGNC Symbol;Acc:HGNC:23586]"}, {"versioned_ensembl_gene_id":"ENSG00000175084.11","gene_symbol":"DES","gene_name":"desmin [Source:HGNC Symbol;Acc:HGNC:2770]","synonyms":"CSM2,CSM1,CMD1I","biotype":"protein_coding","ncbi_id":"1674","summary":"This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. [provided by RefSeq, Jul 2008]","start":219418377,"end":219426739,"strand":1,"description":"desmin [Source:HGNC Symbol;Acc:HGNC:2770]"}, {"versioned_ensembl_gene_id":"ENSG00000081051.7","gene_symbol":"AFP","gene_name":"alpha fetoprotein [Source:HGNC Symbol;Acc:HGNC:317]","synonyms":"HPAFP,FETA","biotype":"protein_coding","ncbi_id":"174","summary":"This gene encodes alpha-fetoprotein, a major plasma protein produced by the yolk sac and the liver during fetal life. Alpha-fetoprotein expression in adults is often associated with hepatocarcinoma and with teratoma, and has prognostic value for managing advanced gastric cancer. However, hereditary persistance of alpha-fetoprotein may also be found in individuals with no obvious pathology. The protein is thought to be the fetal counterpart of serum albumin, and the alpha-fetoprotein and albumin genes are present in tandem in the same transcriptional orientation on chromosome 4. Alpha-fetoprotein is found in monomeric as well as dimeric and trimeric forms, and binds copper, nickel, fatty acids and bilirubin. The level of alpha-fetoprotein in amniotic fluid is used to measure renal loss of protein to screen for spina bifida and anencephaly. [provided by RefSeq, Oct 2019]","start":73431138,"end":73456174,"strand":1,"description":"alpha fetoprotein [Source:HGNC Symbol;Acc:HGNC:317]"}, {"versioned_ensembl_gene_id":"ENSG00000235492.1","gene_symbol":"LINC01221","gene_name":"long intergenic non-protein coding RNA 1221 [Source:HGNC Symbol;Acc:HGNC:49671]","synonyms":"TCONS_00000366","biotype":"lincRNA","ncbi_id":"104266961","summary":null,"start":199016133,"end":199076735,"strand":1,"description":"long intergenic non-protein coding RNA 1221 [Source:HGNC Symbol;Acc:HGNC:49671]"}, {"versioned_ensembl_gene_id":"ENSG00000233410.1","gene_symbol":"LINC01222","gene_name":"long intergenic non-protein coding RNA 1222 [Source:HGNC Symbol;Acc:HGNC:49672]","synonyms":"TCONS_00000112","biotype":"lincRNA","ncbi_id":"102800316","summary":null,"start":199006040,"end":199021037,"strand":-1,"description":"long intergenic non-protein coding RNA 1222 [Source:HGNC Symbol;Acc:HGNC:49672]"}, {"versioned_ensembl_gene_id":"ENSG00000141002.19","gene_symbol":"TCF25","gene_name":"transcription factor 25 [Source:HGNC Symbol;Acc:HGNC:29181]","synonyms":"Nulp1,KIAA1049","biotype":"protein_coding","ncbi_id":"22980","summary":"TCF25 is a member of the basic helix-loop-helix (bHLH) family of transcription factors that are important in embryonic development (Steen and Lindholm, 2008 [PubMed 18068114]).[supplied by OMIM, Sep 2008]","start":89873570,"end":89913627,"strand":1,"description":"transcription factor 25 [Source:HGNC Symbol;Acc:HGNC:29181]"}, {"versioned_ensembl_gene_id":"ENSG00000183695.2","gene_symbol":"MRGPRX2","gene_name":"MAS related GPR family member X2 [Source:HGNC Symbol;Acc:HGNC:17983]","synonyms":"MRGX2","biotype":"protein_coding","ncbi_id":"117194","summary":null,"start":19054455,"end":19060681,"strand":-1,"description":"MAS related GPR family member X2 [Source:HGNC Symbol;Acc:HGNC:17983]"}, {"versioned_ensembl_gene_id":"ENSG00000261017.1","gene_symbol":"AC096996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48059671,"end":48059995,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267048.1","gene_symbol":"AC092143.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":89906157,"end":89918233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248294.1","gene_symbol":"AC008780.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57574027,"end":57614341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052802.12","gene_symbol":"MSMO1","gene_name":"methylsterol monooxygenase 1 [Source:HGNC Symbol;Acc:HGNC:10545]","synonyms":"SC4MOL,ERG25,DESP4","biotype":"protein_coding","ncbi_id":"6307","summary":"Sterol-C4-mehtyl oxidase-like protein was isolated based on its similarity to the yeast ERG25 protein. It contains a set of putative metal binding motifs with similarity to that seen in a family of membrane desaturases-hydroxylases. The protein is localized to the endoplasmic reticulum membrane and is believed to function in cholesterol biosynthesis. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":165327623,"end":165343160,"strand":1,"description":"methylsterol monooxygenase 1 [Source:HGNC Symbol;Acc:HGNC:10545]"}, {"versioned_ensembl_gene_id":"ENSG00000178172.6","gene_symbol":"SPINK6","gene_name":"serine peptidase inhibitor, Kazal type 6 [Source:HGNC Symbol;Acc:HGNC:29486]","synonyms":"UNQ844,MGC21394,BUSI2","biotype":"protein_coding","ncbi_id":"404203","summary":"The protein encoded by this gene is a Kazal-type serine protease inhibitor that acts on kallikrein-related peptidases in the skin. Two transcript variants the same protein have been found for this gene. [provided by RefSeq, Aug 2010]","start":148202794,"end":148215137,"strand":1,"description":"serine peptidase inhibitor, Kazal type 6 [Source:HGNC Symbol;Acc:HGNC:29486]"}, {"versioned_ensembl_gene_id":"ENSG00000131018.22","gene_symbol":"SYNE1","gene_name":"spectrin repeat containing nuclear envelope protein 1 [Source:HGNC Symbol;Acc:HGNC:17089]","synonyms":"SYNE-1B,SCAR8,Nesprin-1,Nesp1,MYNE1,KIAA0796,enaptin,dJ45H2.2,CPG2,C6orf98,ARCA1,8B","biotype":"protein_coding","ncbi_id":"23345","summary":"This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":152121684,"end":152637801,"strand":-1,"description":"spectrin repeat containing nuclear envelope protein 1 [Source:HGNC Symbol;Acc:HGNC:17089]"}, {"versioned_ensembl_gene_id":"ENSG00000225453.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30623474,"end":30623740,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000234061.1","gene_symbol":"AC007969.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171492905,"end":171493095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248931.1","gene_symbol":"MTCYBP40","gene_name":"mitochondrially encoded cytochrome b pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52308]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729144","summary":null,"start":97677547,"end":97678681,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:52308]"}, {"versioned_ensembl_gene_id":"ENSG00000241157.1","gene_symbol":"AC104763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60245288,"end":60245647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228782.7","gene_symbol":"MRPL45P2","gene_name":"mitochondrial ribosomal protein L45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29716]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653479","summary":null,"start":47450568,"end":47492492,"strand":-1,"description":"mitochondrial ribosomal protein L45 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29716]"}, {"versioned_ensembl_gene_id":"ENSG00000236190.1","gene_symbol":"Z82210.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86888586,"end":86888816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248295.2","gene_symbol":"DDX43P1","gene_name":"DEAD-box helicase 43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421307","summary":null,"start":115974513,"end":115976275,"strand":-1,"description":"DEAD-box helicase 43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50780]"}, {"versioned_ensembl_gene_id":"ENSG00000227384.2","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32526470,"end":32540151,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000224846.2","gene_symbol":"AL133351.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2989722,"end":2999134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225543.2","gene_symbol":"C6orf15","gene_name":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]","synonyms":"STG","biotype":"protein_coding","ncbi_id":"29113","summary":null,"start":31104994,"end":31106330,"strand":-1,"description":"chromosome 6 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:13927]"}, {"versioned_ensembl_gene_id":"ENSG00000282607.1","gene_symbol":"MGAM","gene_name":"maltase-glucoamylase [Source:HGNC Symbol;Acc:HGNC:7043]","synonyms":"MGA","biotype":"protein_coding","ncbi_id":"8972","summary":"This gene encodes maltase-glucoamylase, which is a brush border membrane enzyme that plays a role in the final steps of digestion of starch. The protein has two catalytic sites identical to those of sucrase-isomaltase, but the proteins are only 59% homologous. Both are members of glycosyl hydrolase family 31, which has a variety of substrate specificities. [provided by RefSeq, Jul 2008]","start":142038524,"end":142106747,"strand":1,"description":"maltase-glucoamylase [Source:HGNC Symbol;Acc:HGNC:7043]"}, {"versioned_ensembl_gene_id":"ENSG00000235678.3","gene_symbol":"OR5AN2P","gene_name":"olfactory receptor family 5 subfamily AN member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15256]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81224","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59309681,"end":59310576,"strand":-1,"description":"olfactory receptor family 5 subfamily AN member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15256]"}, {"versioned_ensembl_gene_id":"ENSG00000274846.2","gene_symbol":"AC171558.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21690124,"end":21691048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087301.8","gene_symbol":"TXNDC16","gene_name":"thioredoxin domain containing 16 [Source:HGNC Symbol;Acc:HGNC:19965]","synonyms":"KIAA1344","biotype":"protein_coding","ncbi_id":"57544","summary":null,"start":52430590,"end":52552522,"strand":-1,"description":"thioredoxin domain containing 16 [Source:HGNC Symbol;Acc:HGNC:19965]"}, {"versioned_ensembl_gene_id":"ENSG00000123104.11","gene_symbol":"ITPR2","gene_name":"inositol 1,4,5-trisphosphate receptor type 2 [Source:HGNC Symbol;Acc:HGNC:6181]","synonyms":"IP3R2,CFAP48","biotype":"protein_coding","ncbi_id":"3709","summary":"The protein encoded by this gene belongs to the inositol 1,4,5-triphosphate receptor family, whose members are second messenger intracellular calcium release channels. These proteins mediate a rise in cytoplasmic calcium in response to receptor activated production of inositol triphosphate. Inositol triphosphate receptor-mediated signaling is involved in many processes including cell migration, cell division, smooth muscle contraction, and neuronal signaling. This protein is a type 2 receptor that consists of a cytoplasmic amino-terminus that binds inositol triphosphate, six membrane-spanning helices that contribute to the ion pore, and a short cytoplasmic carboxy-terminus. A mutation in this gene has been associated with anhidrosis, suggesting that intracellular calcium release mediated by this protein is required for eccrine sweat production. [provided by RefSeq, Apr 2015]","start":26336515,"end":26833198,"strand":-1,"description":"inositol 1,4,5-trisphosphate receptor type 2 [Source:HGNC Symbol;Acc:HGNC:6181]"}, {"versioned_ensembl_gene_id":"ENSG00000086205.16","gene_symbol":"FOLH1","gene_name":"folate hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3788]","synonyms":"NAALAdase,NAALAD1,GCPII,GCP2,FOLH,PSMA,PSM","biotype":"protein_coding","ncbi_id":"2346","summary":"This gene encodes a type II transmembrane glycoprotein belonging to the M28 peptidase family. The protein acts as a glutamate carboxypeptidase on different alternative substrates, including the nutrient folate and the neuropeptide N-acetyl-l-aspartyl-l-glutamate and is expressed in a number of tissues such as prostate, central and peripheral nervous system and kidney. A mutation in this gene may be associated with impaired intestinal absorption of dietary folates, resulting in low blood folate levels and consequent hyperhomocysteinemia. Expression of this protein in the brain may be involved in a number of pathological conditions associated with glutamate excitotoxicity. In the prostate the protein is up-regulated in cancerous cells and is used as an effective diagnostic and prognostic indicator of prostate cancer. This gene likely arose from a duplication event of a nearby chromosomal region. Alternative splicing gives rise to multiple transcript variants encoding several different isoforms. [provided by RefSeq, Jul 2010]","start":49146635,"end":49208670,"strand":-1,"description":"folate hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3788]"}, {"versioned_ensembl_gene_id":"ENSG00000135446.16","gene_symbol":"CDK4","gene_name":"cyclin dependent kinase 4 [Source:HGNC Symbol;Acc:HGNC:1773]","synonyms":"PSK-J3","biotype":"protein_coding","ncbi_id":"1019","summary":"The protein encoded by this gene is a member of the Ser/Thr protein kinase family. This protein is highly similar to the gene products of S. cerevisiae cdc28 and S. pombe cdc2. It is a catalytic subunit of the protein kinase complex that is important for cell cycle G1 phase progression. The activity of this kinase is restricted to the G1-S phase, which is controlled by the regulatory subunits D-type cyclins and CDK inhibitor p16(INK4a). This kinase was shown to be responsible for the phosphorylation of retinoblastoma gene product (Rb). Mutations in this gene as well as in its related proteins including D-type cyclins, p16(INK4a) and Rb were all found to be associated with tumorigenesis of a variety of cancers. Multiple polyadenylation sites of this gene have been reported. [provided by RefSeq, Jul 2008]","start":57747727,"end":57756013,"strand":-1,"description":"cyclin dependent kinase 4 [Source:HGNC Symbol;Acc:HGNC:1773]"}, {"versioned_ensembl_gene_id":"ENSG00000170325.14","gene_symbol":"PRDM10","gene_name":"PR/SET domain 10 [Source:HGNC Symbol;Acc:HGNC:13995]","synonyms":"PFM7,MGC131802,KIAA1231","biotype":"protein_coding","ncbi_id":"56980","summary":"The protein encoded by this gene is a transcription factor that contains C2H2-type zinc-fingers. It also contains a positive regulatory domain, which has been found in several other zinc-finger transcription factors including those involved in B cell differentiation and tumor suppression. Studies of the mouse counterpart suggest that this protein may be involved in the development of the central nerve system (CNS), as well as in the pathogenesis of neuronal storage disease. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":129899706,"end":130002835,"strand":-1,"description":"PR/SET domain 10 [Source:HGNC Symbol;Acc:HGNC:13995]"}, {"versioned_ensembl_gene_id":"ENSG00000114098.17","gene_symbol":"ARMC8","gene_name":"armadillo repeat containing 8 [Source:HGNC Symbol;Acc:HGNC:24999]","synonyms":"VID28,HSPC056,GID5,DKFZP434A043","biotype":"protein_coding","ncbi_id":"25852","summary":null,"start":138187248,"end":138298389,"strand":1,"description":"armadillo repeat containing 8 [Source:HGNC Symbol;Acc:HGNC:24999]"}, {"versioned_ensembl_gene_id":"ENSG00000163297.16","gene_symbol":"ANTXR2","gene_name":"anthrax toxin receptor 2 [Source:HGNC Symbol;Acc:HGNC:21732]","synonyms":"FLJ31074,CMG2,CMG-2","biotype":"protein_coding","ncbi_id":"118429","summary":"This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":79901149,"end":80125454,"strand":-1,"description":"anthrax toxin receptor 2 [Source:HGNC Symbol;Acc:HGNC:21732]"}, {"versioned_ensembl_gene_id":"ENSG00000155542.11","gene_symbol":"SETD9","gene_name":"SET domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28508]","synonyms":"C5orf35,MGC33648","biotype":"protein_coding","ncbi_id":"133383","summary":null,"start":56909260,"end":56925532,"strand":1,"description":"SET domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28508]"}, {"versioned_ensembl_gene_id":"ENSG00000271828.1","gene_symbol":"AC008937.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56927874,"end":56929573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198542.13","gene_symbol":"ITGBL1","gene_name":"integrin subunit beta like 1 [Source:HGNC Symbol;Acc:HGNC:6164]","synonyms":"TIED,OSCP","biotype":"protein_coding","ncbi_id":"9358","summary":"This gene encodes a beta integrin-related protein that is a member of the EGF-like protein family. The encoded protein contains integrin-like cysteine-rich repeats. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":101452593,"end":101720856,"strand":1,"description":"integrin subunit beta like 1 [Source:HGNC Symbol;Acc:HGNC:6164]"}, {"versioned_ensembl_gene_id":"ENSG00000272558.1","gene_symbol":"U91328.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25983812,"end":25999167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166135.13","gene_symbol":"HIF1AN","gene_name":"hypoxia inducible factor 1 alpha subunit inhibitor [Source:HGNC Symbol;Acc:HGNC:17113]","synonyms":"FLJ22027,FLJ20615,FIH1,DKFZp762F1811","biotype":"protein_coding","ncbi_id":"55662","summary":null,"start":100529072,"end":100559998,"strand":1,"description":"hypoxia inducible factor 1 alpha subunit inhibitor [Source:HGNC Symbol;Acc:HGNC:17113]"}, {"versioned_ensembl_gene_id":"ENSG00000215399.2","gene_symbol":"HMGB3P7","gene_name":"high mobility group box 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39299]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420033","summary":null,"start":101801878,"end":101802488,"strand":1,"description":"high mobility group box 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39299]"}, {"versioned_ensembl_gene_id":"ENSG00000174718.11","gene_symbol":"KIAA1551","gene_name":"KIAA1551 [Source:HGNC Symbol;Acc:HGNC:25559]","synonyms":"UTA2-1,FLJ20696,FLJ10652,C12orf35","biotype":"protein_coding","ncbi_id":"55196","summary":null,"start":31959370,"end":31993107,"strand":1,"description":"KIAA1551 [Source:HGNC Symbol;Acc:HGNC:25559]"}, {"versioned_ensembl_gene_id":"ENSG00000258921.1","gene_symbol":"AC009779.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55638912,"end":55659795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258907.2","gene_symbol":"AC009779.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55654558,"end":55655168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254992.1","gene_symbol":"AP001582.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118322789,"end":118323083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244137.1","gene_symbol":"AL512328.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230710698,"end":230795492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273731.1","gene_symbol":"AC007967.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8931069,"end":8931454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231249.1","gene_symbol":"ITPR1-AS1","gene_name":"ITPR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44470]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996539","summary":null,"start":4490891,"end":4493163,"strand":-1,"description":"ITPR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44470]"}, {"versioned_ensembl_gene_id":"ENSG00000125144.13","gene_symbol":"MT1G","gene_name":"metallothionein 1G [Source:HGNC Symbol;Acc:HGNC:7399]","synonyms":"MT1K,MT1","biotype":"protein_coding","ncbi_id":"4495","summary":null,"start":56666731,"end":56668065,"strand":-1,"description":"metallothionein 1G [Source:HGNC Symbol;Acc:HGNC:7399]"}, {"versioned_ensembl_gene_id":"ENSG00000277410.1","gene_symbol":"AL138726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25885419,"end":25885751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215041.9","gene_symbol":"NEURL4","gene_name":"neuralized E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:34410]","synonyms":"KIAA1787","biotype":"protein_coding","ncbi_id":"84461","summary":"The protein encoded by this gene is predicted and it includes two isoforms resulting from two alternatively spliced transcript variants. [provided by RefSeq, Jul 2008]","start":7315628,"end":7329393,"strand":-1,"description":"neuralized E3 ubiquitin protein ligase 4 [Source:HGNC Symbol;Acc:HGNC:34410]"}, {"versioned_ensembl_gene_id":"ENSG00000226354.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29923115,"end":29923300,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000283142.1","gene_symbol":"AL049767.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":45137706,"end":45138976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235905.8","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30241686,"end":30251176,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000225580.2","gene_symbol":"AL358942.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112616703,"end":112617880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250374.3","gene_symbol":"TRIM75P","gene_name":"tripartite motif containing 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:32686]","synonyms":"TRIM75","biotype":"protein_coding","ncbi_id":"391714","summary":null,"start":165059148,"end":165060554,"strand":1,"description":"tripartite motif containing 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:32686]"}, {"versioned_ensembl_gene_id":"ENSG00000271855.1","gene_symbol":"AC073195.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9555899,"end":9556775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176243.9","gene_symbol":"CDV3P1","gene_name":"CDV3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42387]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129736","summary":null,"start":96776945,"end":96777683,"strand":1,"description":"CDV3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42387]"}, {"versioned_ensembl_gene_id":"ENSG00000100577.18","gene_symbol":"GSTZ1","gene_name":"glutathione S-transferase zeta 1 [Source:HGNC Symbol;Acc:HGNC:4643]","synonyms":"MAI,MAAI,GSTZ1-1","biotype":"protein_coding","ncbi_id":"2954","summary":"This gene is a member of the glutathione S-transferase (GSTs) super-family which encodes multifunctional enzymes important in the detoxification of electrophilic molecules, including carcinogens, mutagens, and several therapeutic drugs, by conjugation with glutathione. This enzyme catalyzes the conversion of maleylacetoacetate to fumarylacetoacatate, which is one of the steps in the phenylalanine/tyrosine degradation pathway. Deficiency of a similar gene in mouse causes oxidative stress. Several transcript variants of this gene encode multiple protein isoforms. [provided by RefSeq, Jul 2015]","start":77320884,"end":77331597,"strand":1,"description":"glutathione S-transferase zeta 1 [Source:HGNC Symbol;Acc:HGNC:4643]"}, {"versioned_ensembl_gene_id":"ENSG00000176293.19","gene_symbol":"ZNF135","gene_name":"zinc finger protein 135 [Source:HGNC Symbol;Acc:HGNC:12919]","synonyms":"ZNF78L1,ZNF61,pHZ-17","biotype":"protein_coding","ncbi_id":"7694","summary":null,"start":58059239,"end":58086310,"strand":1,"description":"zinc finger protein 135 [Source:HGNC Symbol;Acc:HGNC:12919]"}, {"versioned_ensembl_gene_id":"ENSG00000251095.6","gene_symbol":"AC097478.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89551356,"end":89726752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254246.1","gene_symbol":"AC011377.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157104788,"end":157114900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127884.4","gene_symbol":"ECHS1","gene_name":"enoyl-CoA hydratase, short chain 1 [Source:HGNC Symbol;Acc:HGNC:3151]","synonyms":"SCEH","biotype":"protein_coding","ncbi_id":"1892","summary":"The protein encoded by this gene functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The gene product is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. [provided by RefSeq, Jul 2008]","start":133362480,"end":133373689,"strand":-1,"description":"enoyl-CoA hydratase, short chain 1 [Source:HGNC Symbol;Acc:HGNC:3151]"}, {"versioned_ensembl_gene_id":"ENSG00000229032.1","gene_symbol":"AL445685.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51980473,"end":51980814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251417.2","gene_symbol":"AC145285.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28802743,"end":28817828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240634.1","gene_symbol":"AC145285.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28813980,"end":28814673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213109.4","gene_symbol":"AL365223.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":136900233,"end":136901529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179919.3","gene_symbol":"OR10A7","gene_name":"olfactory receptor family 10 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:15329]","synonyms":null,"biotype":"protein_coding","ncbi_id":"121364","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55221025,"end":55221975,"strand":1,"description":"olfactory receptor family 10 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:15329]"}, {"versioned_ensembl_gene_id":"ENSG00000181359.5","gene_symbol":"AC096571.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":170581470,"end":170605450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227423.2","gene_symbol":"OR10U1P","gene_name":"olfactory receptor family 10 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15332]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390318","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55193882,"end":55194786,"strand":-1,"description":"olfactory receptor family 10 subfamily U member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15332]"}, {"versioned_ensembl_gene_id":"ENSG00000237552.1","gene_symbol":"AC099060.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76758124,"end":76779267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116679.15","gene_symbol":"IVNS1ABP","gene_name":"influenza virus NS1A binding protein [Source:HGNC Symbol;Acc:HGNC:16951]","synonyms":"NS1-BP,NS-1,ND1,KLHL39,KIAA0850,HSPC068","biotype":"protein_coding","ncbi_id":"10625","summary":null,"start":185296388,"end":185317329,"strand":-1,"description":"influenza virus NS1A binding protein [Source:HGNC Symbol;Acc:HGNC:16951]"}, {"versioned_ensembl_gene_id":"ENSG00000218359.1","gene_symbol":"SUMO2P13","gene_name":"SUMO2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480263","summary":null,"start":17582034,"end":17582305,"strand":1,"description":"SUMO2 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49351]"}, {"versioned_ensembl_gene_id":"ENSG00000264663.1","gene_symbol":"KRT8P34","gene_name":"keratin 8 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39868]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418811","summary":null,"start":39835037,"end":39836080,"strand":-1,"description":"keratin 8 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39868]"}, {"versioned_ensembl_gene_id":"ENSG00000226415.1","gene_symbol":"TPI1P1","gene_name":"triosephosphate isomerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35449]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729708","summary":null,"start":76699789,"end":76700538,"strand":1,"description":"triosephosphate isomerase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35449]"}, {"versioned_ensembl_gene_id":"ENSG00000267316.5","gene_symbol":"AC090409.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61571342,"end":61579456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272855.1","gene_symbol":"AC104458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76636877,"end":76637339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275176.4","gene_symbol":"ACACA","gene_name":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]","synonyms":"ACC,ACAC,ACC1","biotype":"protein_coding","ncbi_id":"31","summary":"Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5' sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":37086456,"end":37411442,"strand":-1,"description":"acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:HGNC:84]"}, {"versioned_ensembl_gene_id":"ENSG00000223905.1","gene_symbol":"AC103592.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76353583,"end":76354246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221983.7","gene_symbol":"UBA52","gene_name":"ubiquitin A-52 residue ribosomal protein fusion product 1 [Source:HGNC Symbol;Acc:HGNC:12458]","synonyms":"MGC57125,MGC126881,MGC126879,L40,HUBCEP52,CEP52,RPL40","biotype":"protein_coding","ncbi_id":"7311","summary":"Ubiquitin is a highly conserved nuclear and cytoplasmic protein that has a major role in targeting cellular proteins for degradation by the 26S proteosome. It is also involved in the maintenance of chromatin structure, the regulation of gene expression, and the stress response. Ubiquitin is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin moiety fused to an unrelated protein. This gene encodes a fusion protein consisting of ubiquitin at the N terminus and ribosomal protein L40 at the C terminus, a C-terminal extension protein (CEP). Multiple processed pseudogenes derived from this gene are present in the genome. [provided by RefSeq, Jul 2008]","start":18571730,"end":18577550,"strand":1,"description":"ubiquitin A-52 residue ribosomal protein fusion product 1 [Source:HGNC Symbol;Acc:HGNC:12458]"}, {"versioned_ensembl_gene_id":"ENSG00000278589.1","gene_symbol":"ZACNP1","gene_name":"zinc activated ion channel pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51915]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101929026","summary":null,"start":108415220,"end":108416639,"strand":1,"description":"zinc activated ion channel pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51915]"}, {"versioned_ensembl_gene_id":"ENSG00000180346.3","gene_symbol":"TIGD2","gene_name":"tigger transposable element derived 2 [Source:HGNC Symbol;Acc:HGNC:18333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"166815","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":89111500,"end":89114899,"strand":1,"description":"tigger transposable element derived 2 [Source:HGNC Symbol;Acc:HGNC:18333]"}, {"versioned_ensembl_gene_id":"ENSG00000105472.12","gene_symbol":"CLEC11A","gene_name":"C-type lectin domain containing 11A [Source:HGNC Symbol;Acc:HGNC:10576]","synonyms":"SCGF,P47,LSLCL,CLECSF3","biotype":"protein_coding","ncbi_id":"6320","summary":"This gene encodes a member of the C-type lectin superfamily. The encoded protein is a secreted sulfated glycoprotein and functions as a growth factor for primitive hematopoietic progenitor cells. An alternative splice variant has been described but its biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":50723329,"end":50725718,"strand":1,"description":"C-type lectin domain containing 11A [Source:HGNC Symbol;Acc:HGNC:10576]"}, {"versioned_ensembl_gene_id":"ENSG00000243256.1","gene_symbol":"RPL30P14","gene_name":"ribosomal protein L30 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36257]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129867","summary":null,"start":61404858,"end":61405205,"strand":-1,"description":"ribosomal protein L30 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36257]"}, {"versioned_ensembl_gene_id":"ENSG00000238113.6","gene_symbol":"LINC01410","gene_name":"long intergenic non-protein coding RNA 1410 [Source:HGNC Symbol;Acc:HGNC:50702]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103352539","summary":null,"start":62801461,"end":62813486,"strand":1,"description":"long intergenic non-protein coding RNA 1410 [Source:HGNC Symbol;Acc:HGNC:50702]"}, {"versioned_ensembl_gene_id":"ENSG00000259276.1","gene_symbol":"AC087286.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85621264,"end":85627689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186038.9","gene_symbol":"HTR3E","gene_name":"5-hydroxytryptamine receptor 3E [Source:HGNC Symbol;Acc:HGNC:24005]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285242","summary":"This locus encodes a 5-hydroxytryptamine (serotonin) receptor subunit. The encoded protein, subunit E, may play a role in neurotransmission in myenteric neurons. Genes encoding subunits C, D and E form a cluster on chromosome 3. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Feb 2012]","start":184097064,"end":184106995,"strand":1,"description":"5-hydroxytryptamine receptor 3E [Source:HGNC Symbol;Acc:HGNC:24005]"}, {"versioned_ensembl_gene_id":"ENSG00000227702.1","gene_symbol":"LINC00111","gene_name":"long intergenic non-protein coding RNA 111 [Source:HGNC Symbol;Acc:HGNC:1262]","synonyms":"NCRNA00111,C21orf21","biotype":"lincRNA","ncbi_id":"54090","summary":null,"start":41679181,"end":41697336,"strand":1,"description":"long intergenic non-protein coding RNA 111 [Source:HGNC Symbol;Acc:HGNC:1262]"}, {"versioned_ensembl_gene_id":"ENSG00000138111.14","gene_symbol":"MFSD13A","gene_name":"major facilitator superfamily domain containing 13A [Source:HGNC Symbol;Acc:HGNC:26196]","synonyms":"C10orf77,bA18I14.8,TMEM180,FLJ22529","biotype":"protein_coding","ncbi_id":"79847","summary":null,"start":102461395,"end":102477045,"strand":1,"description":"major facilitator superfamily domain containing 13A [Source:HGNC Symbol;Acc:HGNC:26196]"}, {"versioned_ensembl_gene_id":"ENSG00000236717.2","gene_symbol":"AL354751.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92150382,"end":92157445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274516.2","gene_symbol":"FAM74A6","gene_name":"family with sequence similarity 74 member A6 [Source:HGNC Symbol;Acc:HGNC:34036]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"653123","summary":null,"start":60929774,"end":60936746,"strand":1,"description":"family with sequence similarity 74 member A6 [Source:HGNC Symbol;Acc:HGNC:34036]"}, {"versioned_ensembl_gene_id":"ENSG00000088682.13","gene_symbol":"COQ9","gene_name":"coenzyme Q9 [Source:HGNC Symbol;Acc:HGNC:25302]","synonyms":"DKFZP434K046,C16orf49","biotype":"protein_coding","ncbi_id":"57017","summary":"This locus represents a mitochondrial ubiquinone biosynthesis gene. The encoded protein is likely necessary for biosynthesis of coenzyme Q10, as mutations at this locus have been associated with autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency.[provided by RefSeq, Sep 2010]","start":57447425,"end":57461275,"strand":1,"description":"coenzyme Q9 [Source:HGNC Symbol;Acc:HGNC:25302]"}, {"versioned_ensembl_gene_id":"ENSG00000157093.8","gene_symbol":"LYZL4","gene_name":"lysozyme like 4 [Source:HGNC Symbol;Acc:HGNC:28387]","synonyms":"MGC26768,LYC4","biotype":"protein_coding","ncbi_id":"131375","summary":"Lysozymes (see LYZ; MIM 153450), especially C-type lysozymes, are well-recognized bacteriolytic factors widely distributed in the animal kingdom and play a mainly protective role in host defense. LYZL4 is a member of a family of lysozyme-like genes (Zhang et al., 2005 [PubMed 16014814]).[supplied by OMIM, Apr 2009]","start":42397078,"end":42410600,"strand":-1,"description":"lysozyme like 4 [Source:HGNC Symbol;Acc:HGNC:28387]"}, {"versioned_ensembl_gene_id":"ENSG00000223598.1","gene_symbol":"AL138733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151088103,"end":151228447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049540.16","gene_symbol":"ELN","gene_name":"elastin [Source:HGNC Symbol;Acc:HGNC:3327]","synonyms":"WS,WBS,SVAS","biotype":"protein_coding","ncbi_id":"2006","summary":"This gene encodes a protein that is one of the two components of elastic fibers. Elastic fibers comprise part of the extracellular matrix and confer elasticity to organs and tissues including the heart, skin, lungs, ligaments, and blood vessels. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Degradation products of the encoded protein, known as elastin-derived peptides or elastokines, bind the elastin receptor complex and other receptors and stimulate migration and proliferation of monocytes and skin fibroblasts. Elastokines can also contribute to cancer progression. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. [provided by RefSeq, Aug 2017]","start":74027789,"end":74069907,"strand":1,"description":"elastin [Source:HGNC Symbol;Acc:HGNC:3327]"}, {"versioned_ensembl_gene_id":"ENSG00000231883.1","gene_symbol":"AL138733.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151196681,"end":151197638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226579.1","gene_symbol":"MTCYBP31","gene_name":"mitochondrially encoded cytochrome b pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:51997]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075136","summary":null,"start":70120353,"end":70121474,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:51997]"}, {"versioned_ensembl_gene_id":"ENSG00000232290.1","gene_symbol":"AL133260.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151054897,"end":151056057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227321.2","gene_symbol":"MTND4P15","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42202]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873240","summary":null,"start":92110865,"end":92111897,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42202]"}, {"versioned_ensembl_gene_id":"ENSG00000232179.1","gene_symbol":"MTATP6P29","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52187]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075315","summary":null,"start":92108858,"end":92108989,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52187]"}, {"versioned_ensembl_gene_id":"ENSG00000066427.21","gene_symbol":"ATXN3","gene_name":"ataxin 3 [Source:HGNC Symbol;Acc:HGNC:7106]","synonyms":"ATX3,SCA3,MJD,JOS","biotype":"protein_coding","ncbi_id":"4287","summary":"Machado-Joseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder. The protein encoded by this gene contains (CAG)n repeats in the coding region, and the expansion of these repeats from the normal 12-44 to 52-86 is one cause of Machado-Joseph disease. There is a negative correlation between the age of onset and CAG repeat numbers. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2016]","start":92038652,"end":92106621,"strand":-1,"description":"ataxin 3 [Source:HGNC Symbol;Acc:HGNC:7106]"}, {"versioned_ensembl_gene_id":"ENSG00000230306.1","gene_symbol":"BANF1P2","gene_name":"barrier to autointegration factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23426]","synonyms":"BANF1L1,bA122K13.8","biotype":"processed_pseudogene","ncbi_id":"414169","summary":null,"start":133344643,"end":133344906,"strand":-1,"description":"barrier to autointegration factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23426]"}, {"versioned_ensembl_gene_id":"ENSG00000251201.8","gene_symbol":"TMED7-TICAM2","gene_name":"TMED7-TICAM2 readthrough [Source:HGNC Symbol;Acc:HGNC:33945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100302736","summary":"This locus represents naturally occurring read-through transcription between the neighboring transmembrane emp24 protein transport domain containing 7 (TMED7) and toll-like receptor adaptor molecule 2 (TICAM2) genes. Alternative splicing results in multiple transcript variants, one of which encodes a fusion protein that shares sequence identity with the products of each individual gene. This fusion product functions to negatively regulate the adaptor MyD88-independent toll-like receptor 4 pathway. [provided by RefSeq, Nov 2010]","start":115578642,"end":115626161,"strand":-1,"description":"TMED7-TICAM2 readthrough [Source:HGNC Symbol;Acc:HGNC:33945]"}, {"versioned_ensembl_gene_id":"ENSG00000168067.11","gene_symbol":"MAP4K2","gene_name":"mitogen-activated protein kinase kinase kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6864]","synonyms":"RAB8IP,GCK,BL44","biotype":"protein_coding","ncbi_id":"5871","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. Although this kinase is found in many tissues, its expression in lymphoid follicles is restricted to the cells of germinal centre, where it may participate in B-cell differentiation. This kinase can be activated by TNF-alpha, and has been shown to specifically activate MAP kinases. This kinase is also found to interact with TNF receptor-associated factor 2 (TRAF2), which is involved in the activation of MAP3K1/MEKK1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":64784914,"end":64803241,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:6864]"}, {"versioned_ensembl_gene_id":"ENSG00000281162.2","gene_symbol":"AC005035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101962056,"end":101987167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253479.5","gene_symbol":"LINC01603","gene_name":"long intergenic non-protein coding RNA 1603 [Source:HGNC Symbol;Acc:HGNC:51652]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505739","summary":null,"start":69425035,"end":69448244,"strand":-1,"description":"long intergenic non-protein coding RNA 1603 [Source:HGNC Symbol;Acc:HGNC:51652]"}, {"versioned_ensembl_gene_id":"ENSG00000246851.1","gene_symbol":"AL157938.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131189910,"end":131194205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219776.2","gene_symbol":"RPL21P67","gene_name":"ribosomal protein L21 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:36139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271180","summary":null,"start":131469059,"end":131469536,"strand":1,"description":"ribosomal protein L21 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:36139]"}, {"versioned_ensembl_gene_id":"ENSG00000253373.1","gene_symbol":"AC021785.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69175579,"end":69178189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226699.1","gene_symbol":"AL360181.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":133345754,"end":133350726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244482.10","gene_symbol":"LILRA6","gene_name":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]","synonyms":"CD85b,LILRB6,ILT8","biotype":"protein_coding","ncbi_id":"79168","summary":null,"start":54236592,"end":54242791,"strand":-1,"description":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]"}, {"versioned_ensembl_gene_id":"ENSG00000249189.1","gene_symbol":"AC245052.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54246101,"end":54247322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282030.1","gene_symbol":"AC211856.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":352806,"end":353888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241846.1","gene_symbol":"AC092451.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25409293,"end":25409445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258485.2","gene_symbol":"SRMP2","gene_name":"spermidine synthase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20034]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326269","summary":null,"start":60919240,"end":60920155,"strand":-1,"description":"spermidine synthase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20034]"}, {"versioned_ensembl_gene_id":"ENSG00000256060.2","gene_symbol":"AC003002.1","gene_name":"Trafficking protein particle complex subunit 2B [Source:UniProtKB/Swiss-Prot;Acc:P0DI82]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57363511,"end":57365353,"strand":1,"description":"Trafficking protein particle complex subunit 2B [Source:UniProtKB/Swiss-Prot;Acc:P0DI82]"}, {"versioned_ensembl_gene_id":"ENSG00000230438.6","gene_symbol":"SERPINB9P1","gene_name":"serpin family B member 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28590]","synonyms":"MGC39372","biotype":"lincRNA","ncbi_id":"221756","summary":null,"start":2854657,"end":2881407,"strand":-1,"description":"serpin family B member 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28590]"}, {"versioned_ensembl_gene_id":"ENSG00000203624.10","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"PTD017,C6orf14,MRPS18-2,HSPC183","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30607204,"end":30615890,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000242186.1","gene_symbol":"AC231760.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149056716,"end":149057166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255523.1","gene_symbol":"AP001652.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58917015,"end":58928689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260058.1","gene_symbol":"AC018767.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8309962,"end":8357860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276238.2","gene_symbol":"NANOGP7","gene_name":"Nanog homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23105]","synonyms":"NANOGP3","biotype":"transcribed_processed_pseudogene","ncbi_id":"414130","summary":null,"start":91604402,"end":91605319,"strand":-1,"description":"Nanog homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:23105]"}, {"versioned_ensembl_gene_id":"ENSG00000134042.12","gene_symbol":"MRO","gene_name":"maestro [Source:HGNC Symbol;Acc:HGNC:24121]","synonyms":"FLJ30140,C18orf3,B29","biotype":"protein_coding","ncbi_id":"83876","summary":"This gene is specifically transcribed in males before and after differentiation of testis, and the encoded protein may play an important role in a mammalian sex determination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":50795120,"end":50825402,"strand":-1,"description":"maestro [Source:HGNC Symbol;Acc:HGNC:24121]"}, {"versioned_ensembl_gene_id":"ENSG00000272130.1","gene_symbol":"AC091946.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21569755,"end":21570045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251141.5","gene_symbol":"AC093297.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44744900,"end":44808777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226429.2","gene_symbol":"AL590399.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62395370,"end":62395678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223367.6","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"KE-3,S18,HKE3,KE3,D6S218E","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33249931,"end":33254431,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000228058.1","gene_symbol":"LINC01736","gene_name":"long intergenic non-protein coding RNA 1736 [Source:HGNC Symbol;Acc:HGNC:52524]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927532","summary":null,"start":230002730,"end":230007162,"strand":1,"description":"long intergenic non-protein coding RNA 1736 [Source:HGNC Symbol;Acc:HGNC:52524]"}, {"versioned_ensembl_gene_id":"ENSG00000182565.8","gene_symbol":"OR4C2P","gene_name":"olfactory receptor family 4 subfamily C member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14696]","synonyms":"OR4C8P","biotype":"unprocessed_pseudogene","ncbi_id":"119750","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48420210,"end":48421273,"strand":1,"description":"olfactory receptor family 4 subfamily C member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14696]"}, {"versioned_ensembl_gene_id":"ENSG00000223516.1","gene_symbol":"AFF2-IT1","gene_name":"AFF2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41334]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874269","summary":null,"start":148546878,"end":148547397,"strand":1,"description":"AFF2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41334]"}, {"versioned_ensembl_gene_id":"ENSG00000233610.1","gene_symbol":"LINC00462","gene_name":"long intergenic non-protein coding RNA 462 [Source:HGNC Symbol;Acc:HGNC:42811]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129597","summary":null,"start":48576974,"end":48578088,"strand":-1,"description":"long intergenic non-protein coding RNA 462 [Source:HGNC Symbol;Acc:HGNC:42811]"}, {"versioned_ensembl_gene_id":"ENSG00000258963.1","gene_symbol":"EDDM3DP","gene_name":"epididymal protein 3D, pseudogene [Source:HGNC Symbol;Acc:HGNC:37707]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128220","summary":null,"start":20734578,"end":20735011,"strand":1,"description":"epididymal protein 3D, pseudogene [Source:HGNC Symbol;Acc:HGNC:37707]"}, {"versioned_ensembl_gene_id":"ENSG00000155008.13","gene_symbol":"APOOL","gene_name":"apolipoprotein O like [Source:HGNC Symbol;Acc:HGNC:24009]","synonyms":"UNQ8193,Mic27,FAM121A,CXorf33,AAIR8193","biotype":"protein_coding","ncbi_id":"139322","summary":"This gene encodes a protein which contains an apolipoprotein O superfamily domain. This domain is found on proteins in circulating lipoprotein complexes. [provided by RefSeq, Sep 2011]","start":85003826,"end":85093316,"strand":1,"description":"apolipoprotein O like [Source:HGNC Symbol;Acc:HGNC:24009]"}, {"versioned_ensembl_gene_id":"ENSG00000227473.1","gene_symbol":"TSSK5P","gene_name":"testis specific serine kinase 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:31931]","synonyms":"TSSK5P1,TSSKps1,TSSK5P2","biotype":"unitary_pseudogene","ncbi_id":"648630","summary":null,"start":144141214,"end":144143664,"strand":-1,"description":"testis specific serine kinase 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:31931]"}, {"versioned_ensembl_gene_id":"ENSG00000168481.8","gene_symbol":"LGI3","gene_name":"leucine rich repeat LGI family member 3 [Source:HGNC Symbol;Acc:HGNC:18711]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203190","summary":null,"start":22146825,"end":22157084,"strand":-1,"description":"leucine rich repeat LGI family member 3 [Source:HGNC Symbol;Acc:HGNC:18711]"}, {"versioned_ensembl_gene_id":"ENSG00000231369.1","gene_symbol":"Z97353.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26886909,"end":26887548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281491.1","gene_symbol":"DNAJB5-AS1","gene_name":"DNAJB5 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:101926900]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926900","summary":null,"start":34985410,"end":34989379,"strand":-1,"description":"DNAJB5 antisense RNA 1 (head to head) [Source:NCBI gene;Acc:101926900]"}, {"versioned_ensembl_gene_id":"ENSG00000257880.1","gene_symbol":"AC078789.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":62139999,"end":62145643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242922.2","gene_symbol":"RPL21P104","gene_name":"ribosomal protein L21 pseudogene 104 [Source:HGNC Symbol;Acc:HGNC:36918]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271435","summary":null,"start":61775923,"end":61776400,"strand":1,"description":"ribosomal protein L21 pseudogene 104 [Source:HGNC Symbol;Acc:HGNC:36918]"}, {"versioned_ensembl_gene_id":"ENSG00000013364.18","gene_symbol":"MVP","gene_name":"major vault protein [Source:HGNC Symbol;Acc:HGNC:7531]","synonyms":"VAULT1,LRP","biotype":"protein_coding","ncbi_id":"9961","summary":"This gene encodes the major component of the vault complex. Vaults are multi-subunit ribonucleoprotein structures that may be involved in nucleo-cytoplasmic transport. The encoded protein may play a role in multiple cellular processes by regulating the MAP kinase, JAK/STAT and phosphoinositide 3-kinase/Akt signaling pathways. The encoded protein also plays a role in multidrug resistance, and expression of this gene may be a prognostic marker for several types of cancer. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2012]","start":29820394,"end":29848039,"strand":1,"description":"major vault protein [Source:HGNC Symbol;Acc:HGNC:7531]"}, {"versioned_ensembl_gene_id":"ENSG00000111859.16","gene_symbol":"NEDD9","gene_name":"neural precursor cell expressed, developmentally down-regulated 9 [Source:HGNC Symbol;Acc:HGNC:7733]","synonyms":"CASS2,CAS-L,HEF1","biotype":"protein_coding","ncbi_id":"4739","summary":"The protein encoded by this gene is a member of the CRK-associated substrates family. Members of this family are adhesion docking molecules that mediate protein-protein interactions for signal transduction pathways. This protein is a focal adhesion protein that acts as a scaffold to regulate signaling complexes important in cell attachment, migration and invasion as well as apoptosis and the cell cycle. This protein has also been reported to have a role in cancer metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":11183298,"end":11382348,"strand":-1,"description":"neural precursor cell expressed, developmentally down-regulated 9 [Source:HGNC Symbol;Acc:HGNC:7733]"}, {"versioned_ensembl_gene_id":"ENSG00000247925.2","gene_symbol":"AL139807.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11173452,"end":11259099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213170.3","gene_symbol":"SAR1AP2","gene_name":"secretion associated Ras related GTPase 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20770]","synonyms":"SAR1P2,Em:AC026226.2,SARA1P","biotype":"processed_pseudogene","ncbi_id":"641312","summary":null,"start":126272818,"end":126273411,"strand":1,"description":"secretion associated Ras related GTPase 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20770]"}, {"versioned_ensembl_gene_id":"ENSG00000226088.1","gene_symbol":"AL158839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70359562,"end":70360437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223849.1","gene_symbol":"AL354893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95123521,"end":95123868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229065.1","gene_symbol":"AL354893.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95113708,"end":95114461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213761.4","gene_symbol":"MT1P1","gene_name":"metallothionein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23681]","synonyms":"bA435O5.3","biotype":"processed_pseudogene","ncbi_id":"493987","summary":null,"start":95413267,"end":95413449,"strand":-1,"description":"metallothionein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23681]"}, {"versioned_ensembl_gene_id":"ENSG00000278370.1","gene_symbol":"AC021422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90650631,"end":90651103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237503.2","gene_symbol":"AC239798.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143846097,"end":143846504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101104.12","gene_symbol":"PABPC1L","gene_name":"poly(A) binding protein cytoplasmic 1 like [Source:HGNC Symbol;Acc:HGNC:15797]","synonyms":"PABPC1L1,ePAB,dJ1069P2.3,C20orf119","biotype":"protein_coding","ncbi_id":"80336","summary":"This gene belongs to the polyadenylate-binding protein type-1 family of proteins. Members of this family bind to the polyA tails of mRNAs to regulate mRNA stability and translation. The mouse ortholog of this gene is required for female fertility. In human, expression of a functional protein is regulated by alternative splicing. The protein-coding splice variant for this gene is abundantly expressed in human oocytes, while a noncoding splice variant subject to nonsense-mediated decay is the predominant splice variant expressed in somatic tissues. [provided by RefSeq, Aug 2019]","start":44910062,"end":44959035,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 like [Source:HGNC Symbol;Acc:HGNC:15797]"}, {"versioned_ensembl_gene_id":"ENSG00000283183.1","gene_symbol":"AC116565.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":577168,"end":584866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272217.1","gene_symbol":"AL645940.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33246075,"end":33246856,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224531.5","gene_symbol":"SMIM13","gene_name":"small integral membrane protein 13 [Source:HGNC Symbol;Acc:HGNC:27356]","synonyms":"C6orf228","biotype":"protein_coding","ncbi_id":"221710","summary":null,"start":11094033,"end":11138733,"strand":1,"description":"small integral membrane protein 13 [Source:HGNC Symbol;Acc:HGNC:27356]"}, {"versioned_ensembl_gene_id":"ENSG00000130202.9","gene_symbol":"NECTIN2","gene_name":"nectin cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:9707]","synonyms":"PVRR2,PVRL2,PRR2,HVEB,CD112","biotype":"protein_coding","ncbi_id":"5819","summary":"This gene encodes a single-pass type I membrane glycoprotein with two Ig-like C2-type domains and an Ig-like V-type domain. This protein is one of the plasma membrane components of adherens junctions. It also serves as an entry for certain mutant strains of herpes simplex virus and pseudorabies virus, and it is involved in cell to cell spreading of these viruses. Variations in this gene have been associated with differences in the severity of multiple sclerosis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":44846175,"end":44889228,"strand":1,"description":"nectin cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:9707]"}, {"versioned_ensembl_gene_id":"ENSG00000283740.1","gene_symbol":"AC233724.16","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17604177,"end":17605377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250787.1","gene_symbol":"HMGN1P17","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874443","summary":null,"start":56381781,"end":56382075,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39361]"}, {"versioned_ensembl_gene_id":"ENSG00000261373.1","gene_symbol":"VPS9D1-AS1","gene_name":"VPS9D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48915]","synonyms":"MYU","biotype":"antisense_RNA","ncbi_id":"100128881","summary":null,"start":89711856,"end":89718165,"strand":1,"description":"VPS9D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48915]"}, {"versioned_ensembl_gene_id":"ENSG00000258554.1","gene_symbol":"AC025162.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55966838,"end":55967474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151005.4","gene_symbol":"TKTL2","gene_name":"transketolase like 2 [Source:HGNC Symbol;Acc:HGNC:25313]","synonyms":"FLJ32975,DKFZP434L1717","biotype":"protein_coding","ncbi_id":"84076","summary":null,"start":163471093,"end":163473746,"strand":-1,"description":"transketolase like 2 [Source:HGNC Symbol;Acc:HGNC:25313]"}, {"versioned_ensembl_gene_id":"ENSG00000152127.8","gene_symbol":"MGAT5","gene_name":"mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7049]","synonyms":"GNT-V","biotype":"protein_coding","ncbi_id":"4249","summary":"The protein encoded by this gene belongs to the glycosyltransferase family. It catalyzes the addition of beta-1,6-N-acetylglucosamine to the alpha-linked mannose of biantennary N-linked oligosaccharides present on the newly synthesized glycoproteins. It is one of the most important enzymes involved in the regulation of the biosynthesis of glycoprotein oligosaccharides. Alterations of the oligosaccharides on cell surface glycoproteins cause significant changes in the adhesive or migratory behavior of a cell. Increase in the activity of this enzyme has been correlated with the progression of invasive malignancies. [provided by RefSeq, Oct 2011]","start":134119983,"end":134454621,"strand":1,"description":"mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7049]"}, {"versioned_ensembl_gene_id":"ENSG00000147471.11","gene_symbol":"PLPBP","gene_name":"pyridoxal phosphate binding protein [Source:HGNC Symbol;Acc:HGNC:9457]","synonyms":"PROSC","biotype":"protein_coding","ncbi_id":"11212","summary":"This gene encodes a pyridoxal 5'-phosphate binding protein involved in the homeostatic regulation of intracellular pyridoxal 5'-phosphate. This gene has a tumor suppressive effect on hepatocellular carcinoma and other solid tumors of epithelial origin. Naturally occurring mutations in this gene are associated with a pyridoxine-dependent epilepsy. [provided by RefSeq, Mar 2017]","start":37762593,"end":37779767,"strand":1,"description":"pyridoxal phosphate binding protein [Source:HGNC Symbol;Acc:HGNC:9457]"}, {"versioned_ensembl_gene_id":"ENSG00000283360.1","gene_symbol":"AL592295.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161403409,"end":161470523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215840.3","gene_symbol":"AL592295.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161406068,"end":161407082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152439.12","gene_symbol":"ZNF773","gene_name":"zinc finger protein 773 [Source:HGNC Symbol;Acc:HGNC:30487]","synonyms":"ZNF419B,MGC4728","biotype":"protein_coding","ncbi_id":"374928","summary":null,"start":57499915,"end":57518404,"strand":1,"description":"zinc finger protein 773 [Source:HGNC Symbol;Acc:HGNC:30487]"}, {"versioned_ensembl_gene_id":"ENSG00000250025.2","gene_symbol":"AC011396.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146307098,"end":146376963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273341.1","gene_symbol":"AC004921.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77416673,"end":77425443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229745.1","gene_symbol":"BPY2DP","gene_name":"basic charge, Y-linked, 2D, pseudogene [Source:HGNC Symbol;Acc:HGNC:38794]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100885797","summary":null,"start":7932997,"end":7937640,"strand":-1,"description":"basic charge, Y-linked, 2D, pseudogene [Source:HGNC Symbol;Acc:HGNC:38794]"}, {"versioned_ensembl_gene_id":"ENSG00000256777.1","gene_symbol":"PDCL3P7","gene_name":"phosducin-like 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44508]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390340","summary":null,"start":66275940,"end":66276651,"strand":-1,"description":"phosducin-like 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44508]"}, {"versioned_ensembl_gene_id":"ENSG00000242246.2","gene_symbol":"AL603908.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153666466,"end":153666666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223867.1","gene_symbol":"AC098592.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16938225,"end":16938557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227965.1","gene_symbol":"AC098592.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16888621,"end":16888885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234704.9","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"BRD2-IT1,FSRG1,NAT,D6S113E,KIAA9001,RING3","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":33122451,"end":33135290,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000188779.10","gene_symbol":"SKOR1","gene_name":"SKI family transcriptional corepressor 1 [Source:HGNC Symbol;Acc:HGNC:21326]","synonyms":"LBXCOR1,FUSSEL15,CORL1","biotype":"protein_coding","ncbi_id":"390598","summary":null,"start":67819704,"end":67834561,"strand":1,"description":"SKI family transcriptional corepressor 1 [Source:HGNC Symbol;Acc:HGNC:21326]"}, {"versioned_ensembl_gene_id":"ENSG00000188662.6","gene_symbol":"HILS1","gene_name":"histone linker H1 domain, spermatid-specific 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30616]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"373861","summary":"This locus is the ortholog of a mouse protein-coding gene that displays characteristics of a linker histone and is expressed in nuclei of late maturing spermatids. The human locus is expressed; however, the open reading frame has been disrupted by a frameshift so it is unlikely to encode a functional protein. [provided by RefSeq, Oct 2008]","start":50171428,"end":50181178,"strand":-1,"description":"histone linker H1 domain, spermatid-specific 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30616]"}, {"versioned_ensembl_gene_id":"ENSG00000230046.1","gene_symbol":"BIRC6-AS1","gene_name":"BIRC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40641]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874009","summary":null,"start":32377631,"end":32379599,"strand":-1,"description":"BIRC6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40641]"}, {"versioned_ensembl_gene_id":"ENSG00000243189.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":33102388,"end":33124507,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000219681.2","gene_symbol":"AL590084.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25218688,"end":25219069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240110.1","gene_symbol":"AL935026.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32588198,"end":32590793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270831.1","gene_symbol":"NF1P1","gene_name":"neurofibromin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7772]","synonyms":"NF1HHS","biotype":"unprocessed_pseudogene","ncbi_id":"100419006","summary":null,"start":20916686,"end":20935658,"strand":-1,"description":"neurofibromin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7772]"}, {"versioned_ensembl_gene_id":"ENSG00000225449.3","gene_symbol":"RAB6C-AS1","gene_name":"RAB6C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49278]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100131320","summary":null,"start":129966592,"end":129980466,"strand":-1,"description":"RAB6C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49278]"}, {"versioned_ensembl_gene_id":"ENSG00000278326.4","gene_symbol":"PPP4R4","gene_name":"protein phosphatase 4 regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:23788]","synonyms":"PP4R4,KIAA1622,CFAP14","biotype":"protein_coding","ncbi_id":"57718","summary":"The protein encoded by this gene is a HEAT-like repeat-containing protein. The HEAT repeat is a tandemly repeated, 37-47 amino acid long module occurring in a number of cytoplasmic proteins. Arrays of HEAT repeats form a rod-like helical structure and appear to function as protein-protein interaction surfaces. The repeat-containing region of this protein has some similarity to the constant regulatory domain of the protein phosphatase 2A PR65/A subunit. The encoded protein binds protein serine/threonine phosphatase 4c in the cytoplasm. [provided by RefSeq, Jan 2017]","start":94146128,"end":94279735,"strand":1,"description":"protein phosphatase 4 regulatory subunit 4 [Source:HGNC Symbol;Acc:HGNC:23788]"}, {"versioned_ensembl_gene_id":"ENSG00000255351.1","gene_symbol":"AC023946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11352426,"end":11353307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275018.6","gene_symbol":"AL121581.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":64211718,"end":64278487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126549.9","gene_symbol":"STATH","gene_name":"statherin [Source:HGNC Symbol;Acc:HGNC:11369]","synonyms":"STR","biotype":"protein_coding","ncbi_id":"6779","summary":null,"start":69995930,"end":70002570,"strand":1,"description":"statherin [Source:HGNC Symbol;Acc:HGNC:11369]"}, {"versioned_ensembl_gene_id":"ENSG00000255713.2","gene_symbol":"OR4D2","gene_name":"olfactory receptor family 4 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8294]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124538","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58166982,"end":58171411,"strand":1,"description":"olfactory receptor family 4 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8294]"}, {"versioned_ensembl_gene_id":"ENSG00000260868.1","gene_symbol":"LINC01960","gene_name":"long intergenic non-protein coding RNA 1960 [Source:HGNC Symbol;Acc:HGNC:52785]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128905","summary":null,"start":174025280,"end":174027163,"strand":1,"description":"long intergenic non-protein coding RNA 1960 [Source:HGNC Symbol;Acc:HGNC:52785]"}, {"versioned_ensembl_gene_id":"ENSG00000144560.14","gene_symbol":"VGLL4","gene_name":"vestigial like family member 4 [Source:HGNC Symbol;Acc:HGNC:28966]","synonyms":"KIAA0121","biotype":"protein_coding","ncbi_id":"9686","summary":null,"start":11556070,"end":11771350,"strand":-1,"description":"vestigial like family member 4 [Source:HGNC Symbol;Acc:HGNC:28966]"}, {"versioned_ensembl_gene_id":"ENSG00000238086.5","gene_symbol":"PPP1R26P1","gene_name":"protein phosphatase 1 regulatory subunit 26 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42015]","synonyms":"KIAA0649P1","biotype":"processed_pseudogene","ncbi_id":"100418740","summary":null,"start":48316863,"end":48320475,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 26 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42015]"}, {"versioned_ensembl_gene_id":"ENSG00000250822.1","gene_symbol":"LINC02111","gene_name":"long intergenic non-protein coding RNA 2111 [Source:HGNC Symbol;Acc:HGNC:52966]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401177","summary":null,"start":17378906,"end":17387310,"strand":-1,"description":"long intergenic non-protein coding RNA 2111 [Source:HGNC Symbol;Acc:HGNC:52966]"}, {"versioned_ensembl_gene_id":"ENSG00000185442.12","gene_symbol":"FAM174B","gene_name":"family with sequence similarity 174 member B [Source:HGNC Symbol;Acc:HGNC:34339]","synonyms":"MGC102891,LOC400451","biotype":"protein_coding","ncbi_id":"400451","summary":null,"start":92617443,"end":92809884,"strand":-1,"description":"family with sequence similarity 174 member B [Source:HGNC Symbol;Acc:HGNC:34339]"}, {"versioned_ensembl_gene_id":"ENSG00000224537.1","gene_symbol":"MEP1AP4","gene_name":"meprin A subunit alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39138]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643157","summary":null,"start":42817105,"end":42823213,"strand":-1,"description":"meprin A subunit alpha pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39138]"}, {"versioned_ensembl_gene_id":"ENSG00000272681.2","gene_symbol":"FAM223B","gene_name":"family with sequence similarity 223 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34048]","synonyms":"NCRNA00204B,LINC00204B,CXorf52B","biotype":"lincRNA","ncbi_id":"286967","summary":null,"start":154632470,"end":154633182,"strand":-1,"description":"family with sequence similarity 223 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:34048]"}, {"versioned_ensembl_gene_id":"ENSG00000175550.7","gene_symbol":"DRAP1","gene_name":"DR1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:3019]","synonyms":"NC2-alpha","biotype":"protein_coding","ncbi_id":"10589","summary":"Transcriptional repression is a general mechanism for regulating transcriptional initiation in organisms ranging from yeast to humans. Accurate initiation of transcription from eukaryotic protein-encoding genes requires the assembly of a large multiprotein complex consisting of RNA polymerase II and general transcription factors such as TFIIA, TFIIB, and TFIID. DR1 is a repressor that interacts with the TATA-binding protein (TBP) of TFIID and prevents the formation of an active transcription complex by precluding the entry of TFIIA and/or TFIIB into the preinitiation complex. The protein encoded by this gene is a corepressor of transcription that interacts with DR1 to enhance DR1-mediated repression. The interaction between this corepressor and DR1 is required for corepressor function and appears to stabilize the TBP-DR1-DNA complex. [provided by RefSeq, Jul 2008]","start":65919257,"end":65921561,"strand":1,"description":"DR1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:3019]"}, {"versioned_ensembl_gene_id":"ENSG00000001561.6","gene_symbol":"ENPP4","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 4 (putative) [Source:HGNC Symbol;Acc:HGNC:3359]","synonyms":"NPP4,KIAA0879","biotype":"protein_coding","ncbi_id":"22875","summary":null,"start":46129993,"end":46146699,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 4 (putative) [Source:HGNC Symbol;Acc:HGNC:3359]"}, {"versioned_ensembl_gene_id":"ENSG00000111850.10","gene_symbol":"SMIM8","gene_name":"small integral membrane protein 8 [Source:HGNC Symbol;Acc:HGNC:21401]","synonyms":"DKFZP586E1923,dJ102H19.2,C6orf162","biotype":"protein_coding","ncbi_id":"57150","summary":null,"start":87322583,"end":87399749,"strand":1,"description":"small integral membrane protein 8 [Source:HGNC Symbol;Acc:HGNC:21401]"}, {"versioned_ensembl_gene_id":"ENSG00000251435.1","gene_symbol":"C1GALT1P2","gene_name":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128603","summary":null,"start":56192530,"end":56193633,"strand":1,"description":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51615]"}, {"versioned_ensembl_gene_id":"ENSG00000186326.3","gene_symbol":"RGS9BP","gene_name":"regulator of G protein signaling 9 binding protein [Source:HGNC Symbol;Acc:HGNC:30304]","synonyms":"RGS9,R9AP,PERRS,FLJ45744","biotype":"protein_coding","ncbi_id":"388531","summary":"The protein encoded by this gene functions as a regulator of G protein-coupled receptor signaling in phototransduction. Studies in bovine and mouse show that this gene is expressed only in the retina, and is localized in the rod outer segment membranes. This protein is associated with a heterotetrameric complex, specifically interacting with the regulator of G-protein signaling 9, and appears to function as the membrane anchor for the other largely soluble interacting partners. Mutations in this gene are associated with prolonged electroretinal response suppression (PERRS), also known as bradyopsia. [provided by RefSeq, Mar 2010]","start":32675407,"end":32678300,"strand":1,"description":"regulator of G protein signaling 9 binding protein [Source:HGNC Symbol;Acc:HGNC:30304]"}, {"versioned_ensembl_gene_id":"ENSG00000164411.11","gene_symbol":"GJB7","gene_name":"gap junction protein beta 7 [Source:HGNC Symbol;Acc:HGNC:16690]","synonyms":"CX25,bA136M9.1","biotype":"protein_coding","ncbi_id":"375519","summary":"Connexins, such as GJB7, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]","start":87282978,"end":87329278,"strand":-1,"description":"gap junction protein beta 7 [Source:HGNC Symbol;Acc:HGNC:16690]"}, {"versioned_ensembl_gene_id":"ENSG00000206305.12","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32570792,"end":32577071,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000258851.1","gene_symbol":"AL139300.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103553421,"end":103561877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243592.1","gene_symbol":"AC016638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56136979,"end":56137531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226261.1","gene_symbol":"AC064836.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202336024,"end":202336727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276128.1","gene_symbol":"AL591441.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42981772,"end":42988167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274577.2","gene_symbol":"LHX1","gene_name":"LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6593]","synonyms":"LIM1,LIM-1","biotype":"protein_coding","ncbi_id":"3975","summary":"This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor important for the development of the renal and urogenital systems. This gene is a candidate for Mayer-Rokitansky-Kuster-Hauser syndrome, a disorder characterized by anomalies in the female genital tract. [provided by RefSeq, Dec 2010]","start":36938617,"end":36946445,"strand":1,"description":"LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6593]"}, {"versioned_ensembl_gene_id":"ENSG00000277730.2","gene_symbol":"SCGB1C2","gene_name":"secretoglobin family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:51242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653486","summary":null,"start":137526,"end":139067,"strand":1,"description":"secretoglobin family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:51242]"}, {"versioned_ensembl_gene_id":"ENSG00000261072.2","gene_symbol":"AC084783.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56192353,"end":56193262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185631.7","gene_symbol":"AC017079.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128203361,"end":128203775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278631.1","gene_symbol":"AC097374.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94861362,"end":94862667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198860.11","gene_symbol":"TSEN15","gene_name":"tRNA splicing endonuclease subunit 15 [Source:HGNC Symbol;Acc:HGNC:16791]","synonyms":"C1orf19","biotype":"protein_coding","ncbi_id":"116461","summary":"This gene encodes a subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from tRNA precursors. Alternative splicing results in multiple transcript variants. There is a pseudogene of this gene on chromosome 17. [provided by RefSeq, Jul 2014]","start":184051677,"end":184074212,"strand":1,"description":"tRNA splicing endonuclease subunit 15 [Source:HGNC Symbol;Acc:HGNC:16791]"}, {"versioned_ensembl_gene_id":"ENSG00000221988.12","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32153441,"end":32163680,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000143612.19","gene_symbol":"C1orf43","gene_name":"chromosome 1 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:29876]","synonyms":"NICE-3,DKFZp586G1722","biotype":"protein_coding","ncbi_id":"25912","summary":null,"start":154206706,"end":154220637,"strand":-1,"description":"chromosome 1 open reading frame 43 [Source:HGNC Symbol;Acc:HGNC:29876]"}, {"versioned_ensembl_gene_id":"ENSG00000281912.1","gene_symbol":"LINC01144","gene_name":"long intergenic non-protein coding RNA 1144 [Source:NCBI gene;Acc:400752]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400752","summary":null,"start":45303910,"end":45305619,"strand":1,"description":"long intergenic non-protein coding RNA 1144 [Source:NCBI gene;Acc:400752]"}, {"versioned_ensembl_gene_id":"ENSG00000188931.3","gene_symbol":"CFAP126","gene_name":"cilia and flagella associated protein 126 [Source:HGNC Symbol;Acc:HGNC:32325]","synonyms":"Fltp,Flattop,C1orf192","biotype":"protein_coding","ncbi_id":"257177","summary":null,"start":161364731,"end":161367874,"strand":-1,"description":"cilia and flagella associated protein 126 [Source:HGNC Symbol;Acc:HGNC:32325]"}, {"versioned_ensembl_gene_id":"ENSG00000278215.1","gene_symbol":"AP001318.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126376773,"end":126376893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270685.1","gene_symbol":"IGHV1OR15-6","gene_name":"immunoglobulin heavy variable 1/OR15-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5568]","synonyms":"IGHV1/OR15-6","biotype":"IG_V_pseudogene","ncbi_id":"28320","summary":null,"start":20639464,"end":20639890,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5568]"}, {"versioned_ensembl_gene_id":"ENSG00000196748.9","gene_symbol":"CLPSL2","gene_name":"colipase like 2 [Source:HGNC Symbol;Acc:HGNC:21250]","synonyms":"UNQ3045,dJ510O8.5,C6orf126","biotype":"protein_coding","ncbi_id":"389383","summary":null,"start":35776594,"end":35779552,"strand":1,"description":"colipase like 2 [Source:HGNC Symbol;Acc:HGNC:21250]"}, {"versioned_ensembl_gene_id":"ENSG00000258707.2","gene_symbol":"AC023310.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20626819,"end":20627365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188994.12","gene_symbol":"ZNF292","gene_name":"zinc finger protein 292 [Source:HGNC Symbol;Acc:HGNC:18410]","synonyms":"Zn-16,Zn-15,ZFP292,KIAA0530,bA393I2.3","biotype":"protein_coding","ncbi_id":"23036","summary":"This gene encodes a growth hormone-dependent, zinc finger transcription factor that functions as a tumor suppressor. Naturally occurring mutations in this gene are associated with gastric cancer, colorectal cancer, and chronic lymphocytic leukemia. [provided by RefSeq, May 2017]","start":87152833,"end":87264196,"strand":1,"description":"zinc finger protein 292 [Source:HGNC Symbol;Acc:HGNC:18410]"}, {"versioned_ensembl_gene_id":"ENSG00000260505.1","gene_symbol":"AC096644.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220401122,"end":220404033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102359.6","gene_symbol":"SRPX2","gene_name":"sushi repeat containing protein, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:30668]","synonyms":"SRPUL","biotype":"protein_coding","ncbi_id":"27286","summary":"This gene encodes a secreted protein that contains three sushi repeat motifs. The encoded protein may play a role in the development of speech and language centers in the brain. This protein may also be involved in angiogenesis. Mutations in this gene are the cause of bilateral perisylvian polymicrogyria, rolandic epilepsy, speech dyspraxia and cognitive disability. [provided by RefSeq, May 2010]","start":100644166,"end":100675788,"strand":1,"description":"sushi repeat containing protein, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:30668]"}, {"versioned_ensembl_gene_id":"ENSG00000253407.1","gene_symbol":"AC087341.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131130388,"end":131144881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240311.1","gene_symbol":"AC004224.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3496201,"end":3496768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171954.12","gene_symbol":"CYP4F22","gene_name":"cytochrome P450 family 4 subfamily F member 22 [Source:HGNC Symbol;Acc:HGNC:26820]","synonyms":"FLJ39501","biotype":"protein_coding","ncbi_id":"126410","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is part of a cluster of cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12(R)-lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3. [provided by RefSeq, Jul 2008]","start":15508493,"end":15552317,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 22 [Source:HGNC Symbol;Acc:HGNC:26820]"}, {"versioned_ensembl_gene_id":"ENSG00000100852.12","gene_symbol":"ARHGAP5","gene_name":"Rho GTPase activating protein 5 [Source:HGNC Symbol;Acc:HGNC:675]","synonyms":"RhoGAP5,p190BRhoGAP,p190-B,GFI2","biotype":"protein_coding","ncbi_id":"394","summary":"Rho GTPase activating protein 5 negatively regulates RHO GTPases, a family which may mediate cytoskeleton changes by stimulating the hydrolysis of bound GTP. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32076114,"end":32159728,"strand":1,"description":"Rho GTPase activating protein 5 [Source:HGNC Symbol;Acc:HGNC:675]"}, {"versioned_ensembl_gene_id":"ENSG00000258655.2","gene_symbol":"ARHGAP5-AS1","gene_name":"ARHGAP5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:20279]","synonyms":"MGC15504,C14orf128","biotype":"antisense_RNA","ncbi_id":"84837","summary":null,"start":32074946,"end":32076793,"strand":-1,"description":"ARHGAP5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:20279]"}, {"versioned_ensembl_gene_id":"ENSG00000236113.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":30072900,"end":30073777,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000231216.1","gene_symbol":"GS1-600G8.3","gene_name":"unknown transcript [Source:NCBI gene;Acc:100093698]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100093698","summary":null,"start":13310652,"end":13319933,"strand":1,"description":"unknown transcript [Source:NCBI gene;Acc:100093698]"}, {"versioned_ensembl_gene_id":"ENSG00000196116.7","gene_symbol":"TDRD7","gene_name":"tudor domain containing 7 [Source:HGNC Symbol;Acc:HGNC:30831]","synonyms":"PCTAIRE2BP","biotype":"protein_coding","ncbi_id":"23424","summary":"The protein encoded by this gene belongs to the Tudor family of proteins. This protein contains conserved Tudor domains and LOTUS domains. It is a component of RNA granules, which function in RNA processing. Mutations in this gene have been associated with cataract formation in mouse and human. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":97411950,"end":97496125,"strand":1,"description":"tudor domain containing 7 [Source:HGNC Symbol;Acc:HGNC:30831]"}, {"versioned_ensembl_gene_id":"ENSG00000133488.14","gene_symbol":"SEC14L4","gene_name":"SEC14 like lipid binding 4 [Source:HGNC Symbol;Acc:HGNC:20627]","synonyms":"TAP3,dJ130H16.5","biotype":"protein_coding","ncbi_id":"284904","summary":"The protein encoded by this gene is highly similar to the protein encoded by the Saccharomyces cerevisiae SEC14 gene. The SEC14 protein is a phophatidylinositol transfer protein that is essential for biogenesis of Golgi-derived transport vesicles, and thus is required for the export of yeast secretory proteins from the Golgi complex. The specific function of this protein has not yet been determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2009]","start":30488913,"end":30505711,"strand":-1,"description":"SEC14 like lipid binding 4 [Source:HGNC Symbol;Acc:HGNC:20627]"}, {"versioned_ensembl_gene_id":"ENSG00000151413.16","gene_symbol":"NUBPL","gene_name":"nucleotide binding protein like [Source:HGNC Symbol;Acc:HGNC:20278]","synonyms":"IND1,huInd1,FLJ12660,C14orf127","biotype":"protein_coding","ncbi_id":"80224","summary":"This gene encodes a member of the Mrp/NBP35 ATP-binding proteins family. The encoded protein is required for the assembly of the respiratory chain NADH dehydrogenase (complex I), an oligomeric enzymatic complex located in the inner mitochondrial membrane. Mutations in this gene cause mitochondrial complex I deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":31489956,"end":31861224,"strand":1,"description":"nucleotide binding protein like [Source:HGNC Symbol;Acc:HGNC:20278]"}, {"versioned_ensembl_gene_id":"ENSG00000276180.1","gene_symbol":"HIST1H4I","gene_name":"histone cluster 1 H4 family member i [Source:HGNC Symbol;Acc:HGNC:4793]","synonyms":"H4FM,H4/m","biotype":"protein_coding","ncbi_id":"8294","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]","start":27138588,"end":27139881,"strand":1,"description":"histone cluster 1 H4 family member i [Source:HGNC Symbol;Acc:HGNC:4793]"}, {"versioned_ensembl_gene_id":"ENSG00000128016.5","gene_symbol":"ZFP36","gene_name":"ZFP36 ring finger protein [Source:HGNC Symbol;Acc:HGNC:12862]","synonyms":"TTP,TIS11,RNF162A,NUP475,G0S24","biotype":"protein_coding","ncbi_id":"7538","summary":null,"start":39406813,"end":39409412,"strand":1,"description":"ZFP36 ring finger protein [Source:HGNC Symbol;Acc:HGNC:12862]"}, {"versioned_ensembl_gene_id":"ENSG00000169258.6","gene_symbol":"GPRIN1","gene_name":"G protein regulated inducer of neurite outgrowth 1 [Source:HGNC Symbol;Acc:HGNC:24835]","synonyms":"KIAA1893,GRIN1","biotype":"protein_coding","ncbi_id":"114787","summary":null,"start":176595802,"end":176610133,"strand":-1,"description":"G protein regulated inducer of neurite outgrowth 1 [Source:HGNC Symbol;Acc:HGNC:24835]"}, {"versioned_ensembl_gene_id":"ENSG00000257230.1","gene_symbol":"LINC02448","gene_name":"long intergenic non-protein coding RNA 2448 [Source:HGNC Symbol;Acc:HGNC:53380]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369792","summary":null,"start":59523278,"end":59524184,"strand":-1,"description":"long intergenic non-protein coding RNA 2448 [Source:HGNC Symbol;Acc:HGNC:53380]"}, {"versioned_ensembl_gene_id":"ENSG00000181104.6","gene_symbol":"F2R","gene_name":"coagulation factor II thrombin receptor [Source:HGNC Symbol;Acc:HGNC:3537]","synonyms":"TR,PAR1,PAR-1,CF2R","biotype":"protein_coding","ncbi_id":"2149","summary":"Coagulation factor II receptor is a 7-transmembrane receptor involved in the regulation of thrombotic response. Proteolytic cleavage leads to the activation of the receptor. F2R is a G-protein coupled receptor family member. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":76716043,"end":76735781,"strand":1,"description":"coagulation factor II thrombin receptor [Source:HGNC Symbol;Acc:HGNC:3537]"}, {"versioned_ensembl_gene_id":"ENSG00000248431.1","gene_symbol":"AC005150.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162740668,"end":162742048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270614.1","gene_symbol":"AC011451.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9348106,"end":9348703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282755.1","gene_symbol":"AC010724.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":82619121,"end":82635020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261192.1","gene_symbol":"RNF126P1","gene_name":"ring finger protein 126 pseudogene 1 [Source:NCBI gene;Acc:376412]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"376412","summary":null,"start":57045478,"end":57046797,"strand":1,"description":"ring finger protein 126 pseudogene 1 [Source:NCBI gene;Acc:376412]"}, {"versioned_ensembl_gene_id":"ENSG00000225891.1","gene_symbol":"AL513365.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26462756,"end":26467282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000038945.14","gene_symbol":"MSR1","gene_name":"macrophage scavenger receptor 1 [Source:HGNC Symbol;Acc:HGNC:7376]","synonyms":"SR-AIII,SR-AII,SR-AI,SR-A,SCARA1,CD204","biotype":"protein_coding","ncbi_id":"4481","summary":"This gene encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis, Alzheimer's disease, and host defense. The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within the endoplasmic reticulum, making it unable to perform endocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages. [provided by RefSeq, Jul 2008]","start":16107878,"end":16567490,"strand":-1,"description":"macrophage scavenger receptor 1 [Source:HGNC Symbol;Acc:HGNC:7376]"}, {"versioned_ensembl_gene_id":"ENSG00000179583.18","gene_symbol":"CIITA","gene_name":"class II major histocompatibility complex transactivator [Source:HGNC Symbol;Acc:HGNC:7067]","synonyms":"NLRA,MHC2TA,C2TA","biotype":"protein_coding","ncbi_id":"4261","summary":"This gene encodes a protein with an acidic transcriptional activation domain, 4 LRRs (leucine-rich repeats) and a GTP binding domain. The protein is located in the nucleus and acts as a positive regulator of class II major histocompatibility complex gene transcription, and is referred to as the \"master control factor\" for the expression of these genes. The protein also binds GTP and uses GTP binding to facilitate its own transport into the nucleus. Once in the nucleus it does not bind DNA but rather uses an intrinsic acetyltransferase (AT) activity to act in a coactivator-like fashion. Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency), increased susceptibility to rheumatoid arthritis, multiple sclerosis, and possibly myocardial infarction. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":10866222,"end":10932281,"strand":1,"description":"class II major histocompatibility complex transactivator [Source:HGNC Symbol;Acc:HGNC:7067]"}, {"versioned_ensembl_gene_id":"ENSG00000236969.2","gene_symbol":"GGT8P","gene_name":"gamma-glutamyltransferase 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:33438]","synonyms":"GGT1P1,FLJ31276","biotype":"unprocessed_pseudogene","ncbi_id":"645367","summary":null,"start":91775944,"end":91781169,"strand":1,"description":"gamma-glutamyltransferase 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:33438]"}, {"versioned_ensembl_gene_id":"ENSG00000253829.1","gene_symbol":"AC067817.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38844866,"end":38846439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171759.9","gene_symbol":"PAH","gene_name":"phenylalanine hydroxylase [Source:HGNC Symbol;Acc:HGNC:8582]","synonyms":"PH","biotype":"protein_coding","ncbi_id":"5053","summary":"This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]","start":102836885,"end":102958410,"strand":-1,"description":"phenylalanine hydroxylase [Source:HGNC Symbol;Acc:HGNC:8582]"}, {"versioned_ensembl_gene_id":"ENSG00000274927.1","gene_symbol":"AC239859.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143461221,"end":143498767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277095.1","gene_symbol":"AC242852.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143354191,"end":143386122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270777.1","gene_symbol":"AL158042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11001304,"end":11001763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280579.1","gene_symbol":"AC006359.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144627218,"end":144641637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253409.1","gene_symbol":"TRBV7-4","gene_name":"T-cell receptor beta variable 7-4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12238]","synonyms":"TRBV74,TCRBV7S4,TCRBV6S8A2T","biotype":"TR_V_gene","ncbi_id":"28594","summary":null,"start":142455174,"end":142455635,"strand":1,"description":"T-cell receptor beta variable 7-4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12238]"}, {"versioned_ensembl_gene_id":"ENSG00000254774.1","gene_symbol":"AC022239.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11553224,"end":11554207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276851.1","gene_symbol":"AC002401.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50094065,"end":50094647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235090.1","gene_symbol":"RPL7L1P3","gene_name":"ribosomal protein L7 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39485]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131964","summary":null,"start":75922755,"end":75923443,"strand":1,"description":"ribosomal protein L7 like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39485]"}, {"versioned_ensembl_gene_id":"ENSG00000117682.16","gene_symbol":"DHDDS","gene_name":"dehydrodolichyl diphosphate synthase subunit [Source:HGNC Symbol;Acc:HGNC:20603]","synonyms":"RP59,HDS,FLJ13102,DS","biotype":"protein_coding","ncbi_id":"79947","summary":"The protein encoded by this gene catalyzes cis-prenyl chain elongation to produce the polyprenyl backbone of dolichol, a glycosyl carrier lipid required for the biosynthesis of several classes of glycoproteins. Mutations in this gene are associated with retinitis pigmentosa type 59. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":26432282,"end":26471294,"strand":1,"description":"dehydrodolichyl diphosphate synthase subunit [Source:HGNC Symbol;Acc:HGNC:20603]"}, {"versioned_ensembl_gene_id":"ENSG00000254616.1","gene_symbol":"AP001775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134173095,"end":134173680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282111.1","gene_symbol":"AL137793.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":229022773,"end":229038274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169621.9","gene_symbol":"APLF","gene_name":"aprataxin and PNKP like factor [Source:HGNC Symbol;Acc:HGNC:28724]","synonyms":"ZCCHH1,Xip1,MGC47799,C2orf13","biotype":"protein_coding","ncbi_id":"200558","summary":"C2ORF13 is a component of the cellular response to chromosomal DNA single- and double-strand breaks (Iles et al., 2007 [PubMed 17353262]).[supplied by OMIM, Mar 2008]","start":68467561,"end":68655862,"strand":1,"description":"aprataxin and PNKP like factor [Source:HGNC Symbol;Acc:HGNC:28724]"}, {"versioned_ensembl_gene_id":"ENSG00000142634.12","gene_symbol":"EFHD2","gene_name":"EF-hand domain family member D2 [Source:HGNC Symbol;Acc:HGNC:28670]","synonyms":"MGC4342","biotype":"protein_coding","ncbi_id":"79180","summary":null,"start":15409895,"end":15430343,"strand":1,"description":"EF-hand domain family member D2 [Source:HGNC Symbol;Acc:HGNC:28670]"}, {"versioned_ensembl_gene_id":"ENSG00000223894.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33069683,"end":33075225,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000234795.9","gene_symbol":"RFTN1P1","gene_name":"raftlin, lipid raft linker 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23971]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"360015","summary":null,"start":7712985,"end":7809261,"strand":-1,"description":"raftlin, lipid raft linker 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23971]"}, {"versioned_ensembl_gene_id":"ENSG00000245148.2","gene_symbol":"ARAP1-AS2","gene_name":"ARAP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39994]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506020","summary":null,"start":72700474,"end":72705607,"strand":1,"description":"ARAP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39994]"}, {"versioned_ensembl_gene_id":"ENSG00000241549.8","gene_symbol":"GUSBP2","gene_name":"glucuronidase, beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18792]","synonyms":"SMAC3L2,SMAC3L,SMA3-L,GUSBL1,bGLU-Lp,bA239L20.5,bA239L20.1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387036","summary":null,"start":26871484,"end":26956554,"strand":-1,"description":"glucuronidase, beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18792]"}, {"versioned_ensembl_gene_id":"ENSG00000219023.1","gene_symbol":"AL033519.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35555873,"end":35556264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248699.1","gene_symbol":"AC114964.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15450701,"end":15451811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240891.7","gene_symbol":"PLCXD2","gene_name":"phosphatidylinositol specific phospholipase C X domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26462]","synonyms":"FLJ31579","biotype":"protein_coding","ncbi_id":"257068","summary":null,"start":111674676,"end":111846447,"strand":1,"description":"phosphatidylinositol specific phospholipase C X domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26462]"}, {"versioned_ensembl_gene_id":"ENSG00000279526.1","gene_symbol":"AC011239.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23616499,"end":23617987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232696.1","gene_symbol":"AC017006.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46078015,"end":46078828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229802.11","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"ZIP7,HKE4,RING5,H2-KE4,KE4,D6S2244E","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33178351,"end":33182345,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000275214.4","gene_symbol":"IFI27","gene_name":"interferon alpha inducible protein 27 [Source:HGNC Symbol;Acc:HGNC:5397]","synonyms":"P27,ISG12,FAM14D","biotype":"protein_coding","ncbi_id":"3429","summary":null,"start":94104836,"end":94116698,"strand":1,"description":"interferon alpha inducible protein 27 [Source:HGNC Symbol;Acc:HGNC:5397]"}, {"versioned_ensembl_gene_id":"ENSG00000167005.13","gene_symbol":"NUDT21","gene_name":"nudix hydrolase 21 [Source:HGNC Symbol;Acc:HGNC:13870]","synonyms":"CPSF5,CFIM25","biotype":"protein_coding","ncbi_id":"11051","summary":"The protein encoded by this gene is one subunit of a cleavage factor required for 3' RNA cleavage and polyadenylation processing. The interaction of the protein with the RNA is one of the earliest steps in the assembly of the 3' end processing complex and facilitates the recruitment of other processing factors. This gene encodes the 25kD subunit of the protein complex, which is composed of four polypeptides. [provided by RefSeq, Jul 2008]","start":56429133,"end":56452199,"strand":-1,"description":"nudix hydrolase 21 [Source:HGNC Symbol;Acc:HGNC:13870]"}, {"versioned_ensembl_gene_id":"ENSG00000115257.15","gene_symbol":"PCSK4","gene_name":"proprotein convertase subtilisin/kexin type 4 [Source:HGNC Symbol;Acc:HGNC:8746]","synonyms":"SPC5,PC4,MGC34749,DKFZp434B217","biotype":"protein_coding","ncbi_id":"54760","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to subcellular compartments where a second autocatalytic even takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. The protease is expressed only in the testis, placenta, and ovary. It plays a critical role in fertilization, fetoplacental growth, and embryonic development and processes multiple prohormones including pro-pituitary adenylate cyclase-activating protein and pro-insulin-like growth factor II. [provided by RefSeq, Jan 2014]","start":1481428,"end":1490752,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 4 [Source:HGNC Symbol;Acc:HGNC:8746]"}, {"versioned_ensembl_gene_id":"ENSG00000241881.1","gene_symbol":"AC245088.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142285750,"end":142288869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273007.1","gene_symbol":"AC021205.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122881878,"end":122884712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236168.1","gene_symbol":"AL133466.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23980585,"end":23980734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183715.13","gene_symbol":"OPCML","gene_name":"opioid binding protein/cell adhesion molecule like [Source:HGNC Symbol;Acc:HGNC:8143]","synonyms":"OPCM,OBCAM,IGLON1","biotype":"protein_coding","ncbi_id":"4978","summary":"This gene encodes a member of the IgLON subfamily in the immunoglobulin protein superfamily of proteins. The encoded preprotein is proteolytically processed to generate the mature protein. This protein is localized in the plasma membrane and may have an accessory role in opioid receptor function. This gene has an ortholog in rat and bovine. The opioid binding-cell adhesion molecule encoded by the rat gene binds opioid alkaloids in the presence of acidic lipids, exhibits selectivity for mu ligands and acts as a GPI-anchored protein. Since the encoded protein is highly conserved in species during evolution, it may have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":132414977,"end":133532519,"strand":-1,"description":"opioid binding protein/cell adhesion molecule like [Source:HGNC Symbol;Acc:HGNC:8143]"}, {"versioned_ensembl_gene_id":"ENSG00000255371.1","gene_symbol":"OPCML-IT2","gene_name":"OPCML intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41365]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874332","summary":null,"start":132859245,"end":132860077,"strand":-1,"description":"OPCML intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41365]"}, {"versioned_ensembl_gene_id":"ENSG00000043462.11","gene_symbol":"LCP2","gene_name":"lymphocyte cytosolic protein 2 [Source:HGNC Symbol;Acc:HGNC:6529]","synonyms":"SLP76,SLP-76","biotype":"protein_coding","ncbi_id":"3937","summary":"This gene encodes an adapter protein that acts as a substrate of the T cell antigen receptor (TCR)-activated protein tyrosine kinase pathway. The encoded protein associates with growth factor receptor bound protein 2, and is thought to play a role TCR-mediated intracellular signal transduction. A similar protein in mouse plays a role in normal T-cell development and activation. Mice lacking this gene show subcutaneous and intraperitoneal fetal hemorrhaging, dysfunctional platelets and impaired viability. [provided by RefSeq, Nov 2016]","start":170246237,"end":170298227,"strand":-1,"description":"lymphocyte cytosolic protein 2 [Source:HGNC Symbol;Acc:HGNC:6529]"}, {"versioned_ensembl_gene_id":"ENSG00000254123.1","gene_symbol":"AC027701.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82098451,"end":82160577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226140.5","gene_symbol":"AL355339.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16278701,"end":16295858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240775.1","gene_symbol":"AC021205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122840343,"end":122840690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138685.13","gene_symbol":"FGF2","gene_name":"fibroblast growth factor 2 [Source:HGNC Symbol;Acc:HGNC:3676]","synonyms":"FGFB","biotype":"protein_coding","ncbi_id":"2247","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members bind heparin and possess broad mitogenic and angiogenic activities. This protein has been implicated in diverse biological processes, such as limb and nervous system development, wound healing, and tumor growth. The mRNA for this gene contains multiple polyadenylation sites, and is alternatively translated from non-AUG (CUG) and AUG initiation codons, resulting in five different isoforms with distinct properties. The CUG-initiated isoforms are localized in the nucleus and are responsible for the intracrine effect, whereas, the AUG-initiated form is mostly cytosolic and is responsible for the paracrine and autocrine effects of this FGF. [provided by RefSeq, Jul 2008]","start":122826708,"end":122898236,"strand":1,"description":"fibroblast growth factor 2 [Source:HGNC Symbol;Acc:HGNC:3676]"}, {"versioned_ensembl_gene_id":"ENSG00000250247.1","gene_symbol":"SEPHS2P1","gene_name":"selenophosphate synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42165]","synonyms":"SEPHS1P5","biotype":"processed_pseudogene","ncbi_id":"100420190","summary":null,"start":14960232,"end":14961393,"strand":1,"description":"selenophosphate synthetase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42165]"}, {"versioned_ensembl_gene_id":"ENSG00000250662.1","gene_symbol":"HNRNPKP5","gene_name":"heterogeneous nuclear ribonucleoprotein K pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874385","summary":null,"start":14877667,"end":14877919,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein K pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42378]"}, {"versioned_ensembl_gene_id":"ENSG00000224063.5","gene_symbol":"AC007319.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":187003220,"end":187554663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283421.1","gene_symbol":"AF001550.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":21299903,"end":21300506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175311.6","gene_symbol":"ANKS4B","gene_name":"ankyrin repeat and sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:26795]","synonyms":"HARP,FLJ38819","biotype":"protein_coding","ncbi_id":"257629","summary":null,"start":21233665,"end":21253845,"strand":1,"description":"ankyrin repeat and sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:26795]"}, {"versioned_ensembl_gene_id":"ENSG00000251075.1","gene_symbol":"HTT-AS","gene_name":"HTT antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:37118]","synonyms":"HTTAS,HTT-AS1","biotype":"antisense_RNA","ncbi_id":"100750326","summary":null,"start":3063471,"end":3074514,"strand":-1,"description":"HTT antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:37118]"}, {"versioned_ensembl_gene_id":"ENSG00000183691.4","gene_symbol":"NOG","gene_name":"noggin [Source:HGNC Symbol;Acc:HGNC:7866]","synonyms":"SYNS1,SYM1","biotype":"protein_coding","ncbi_id":"9241","summary":"The secreted polypeptide, encoded by this gene, binds and inactivates members of the transforming growth factor-beta (TGF-beta) superfamily signaling proteins, such as bone morphogenetic protein-4 (BMP4). By diffusing through extracellular matrices more efficiently than members of the TGF-beta superfamily, this protein may have a principal role in creating morphogenic gradients. The protein appears to have pleiotropic effect, both early in development as well as in later stages. It was originally isolated from Xenopus based on its ability to restore normal dorsal-ventral body axis in embryos that had been artificially ventralized by UV treatment. The results of the mouse knockout of the ortholog suggest that it is involved in numerous developmental processes, such as neural tube fusion and joint formation. Recently, several dominant human NOG mutations in unrelated families with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1) were identified; both SYM1 and SYNS1 have multiple joint fusion as their principal feature, and map to the same region (17q22) as this gene. All of these mutations altered evolutionarily conserved amino acid residues. The amino acid sequence of this human gene is highly homologous to that of Xenopus, rat and mouse. [provided by RefSeq, Jul 2008]","start":56593699,"end":56595590,"strand":1,"description":"noggin [Source:HGNC Symbol;Acc:HGNC:7866]"}, {"versioned_ensembl_gene_id":"ENSG00000268221.5","gene_symbol":"OPN1MW","gene_name":"opsin 1, medium wave sensitive [Source:HGNC Symbol;Acc:HGNC:4206]","synonyms":"OPN1MW1,GCP,COD5,CBD,CBBM","biotype":"protein_coding","ncbi_id":"2652","summary":"This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009]","start":154182596,"end":154196135,"strand":1,"description":"opsin 1, medium wave sensitive [Source:HGNC Symbol;Acc:HGNC:4206]"}, {"versioned_ensembl_gene_id":"ENSG00000184743.12","gene_symbol":"ATL3","gene_name":"atlastin GTPase 3 [Source:HGNC Symbol;Acc:HGNC:24526]","synonyms":"DKFZP564J0863","biotype":"protein_coding","ncbi_id":"25923","summary":"This gene encodes a member of a family of dynamin-like, integral membrane GTPases. The encoded protein is required for the proper formation of the network of interconnected tubules of the endoplasmic reticulum. Mutations in this gene may be associated with hereditary sensory neuropathy type IF. Alternatively spliced transcript variants that encode distinct isoforms have been described. [provided by RefSeq, Feb 2014]","start":63624087,"end":63671921,"strand":-1,"description":"atlastin GTPase 3 [Source:HGNC Symbol;Acc:HGNC:24526]"}, {"versioned_ensembl_gene_id":"ENSG00000229912.1","gene_symbol":"AC128709.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197450327,"end":197456654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261205.2","gene_symbol":"NIFKP4","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44952]","synonyms":"MKI67IPP4","biotype":"processed_pseudogene","ncbi_id":"100128707","summary":null,"start":75251743,"end":75252934,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44952]"}, {"versioned_ensembl_gene_id":"ENSG00000264179.1","gene_symbol":"AP000894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":856526,"end":857045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141086.17","gene_symbol":"CTRL","gene_name":"chymotrypsin like [Source:HGNC Symbol;Acc:HGNC:2524]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1506","summary":"This gene encodes a serine-type endopeptidase with chymotrypsin- and elastase-2-like activities. The gene encoding this zymogen is expressed specifically in the pancreas and likely functions as a digestive enzyme. [provided by RefSeq, Sep 2016]","start":67927640,"end":67932414,"strand":-1,"description":"chymotrypsin like [Source:HGNC Symbol;Acc:HGNC:2524]"}, {"versioned_ensembl_gene_id":"ENSG00000253663.1","gene_symbol":"NPM1P52","gene_name":"nucleophosmin 1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:45231]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422272","summary":null,"start":103016744,"end":103017589,"strand":1,"description":"nucleophosmin 1 pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:45231]"}, {"versioned_ensembl_gene_id":"ENSG00000242104.4","gene_symbol":"AC092978.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":141660536,"end":141729405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272072.1","gene_symbol":"AC004492.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107192559,"end":107193300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052723.11","gene_symbol":"SIKE1","gene_name":"suppressor of IKBKE 1 [Source:HGNC Symbol;Acc:HGNC:26119]","synonyms":"SIKE,FLJ21168","biotype":"protein_coding","ncbi_id":"80143","summary":"SIKE interacts with IKK-epsilon (IKBKE; MIM 605048) and TBK1 (MIM 604834) and acts as a suppressor of TLR3 (MIM 603029) and virus-triggered interferon activation pathways (Huang et al., 2005 [PubMed 16281057]).[supplied by OMIM, Mar 2008]","start":114769479,"end":114780685,"strand":-1,"description":"suppressor of IKBKE 1 [Source:HGNC Symbol;Acc:HGNC:26119]"}, {"versioned_ensembl_gene_id":"ENSG00000279980.1","gene_symbol":"GABARAPL3","gene_name":"GABA type A receptor associated protein like 3 pseudogene [Source:NCBI gene;Acc:23766]","synonyms":"ATG8D,ATG8D","biotype":"TEC","ncbi_id":"23766","summary":null,"start":90347587,"end":90349437,"strand":1,"description":"GABA type A receptor associated protein like 3 pseudogene [Source:NCBI gene;Acc:23766]"}, {"versioned_ensembl_gene_id":"ENSG00000276720.1","gene_symbol":"CU151838.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54229605,"end":54230979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244125.1","gene_symbol":"AC078882.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":142131178,"end":142137830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236129.1","gene_symbol":"AP002856.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131187022,"end":131189753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262079.1","gene_symbol":"AC007638.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55325757,"end":55327791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198223.16","gene_symbol":"CSF2RA","gene_name":"colony stimulating factor 2 receptor alpha subunit [Source:HGNC Symbol;Acc:HGNC:2435]","synonyms":"CSF2R,CD116","biotype":"protein_coding","ncbi_id":"1438","summary":"The protein encoded by this gene is the alpha subunit of the heterodimeric receptor for colony stimulating factor 2, a cytokine which controls the production, differentiation, and function of granulocytes and macrophages. The encoded protein is a member of the cytokine family of receptors. This gene is found in the pseudoautosomal region (PAR) of the X and Y chromosomes. Multiple transcript variants encoding different isoforms have been found for this gene, with some of the isoforms being membrane-bound and others being soluble. [provided by RefSeq, Jul 2008]","start":1268800,"end":1310381,"strand":1,"description":"colony stimulating factor 2 receptor alpha subunit [Source:HGNC Symbol;Acc:HGNC:2435]"}, {"versioned_ensembl_gene_id":"ENSG00000235560.3","gene_symbol":"AC002310.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30534752,"end":30537144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136146.14","gene_symbol":"MED4","gene_name":"mediator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:17903]","synonyms":"VDRIP,TRAP36,HSPC126,DRIP36","biotype":"protein_coding","ncbi_id":"29079","summary":"This gene encodes a component of the Mediator complex. The Mediator complex interacts with DNA-binding gene-specific transcription factors to modulate transcription by RNA polymerase II. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":48053323,"end":48095131,"strand":-1,"description":"mediator complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:17903]"}, {"versioned_ensembl_gene_id":"ENSG00000236250.8","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31963829,"end":31974100,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000229083.1","gene_symbol":"PSMA6P2","gene_name":"proteasome subunit alpha 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39607]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729412","summary":null,"start":12825840,"end":12826833,"strand":1,"description":"proteasome subunit alpha 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39607]"}, {"versioned_ensembl_gene_id":"ENSG00000267261.5","gene_symbol":"AC099811.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42119674,"end":42154916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072422.16","gene_symbol":"RHOBTB1","gene_name":"Rho related BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18738]","synonyms":"KIAA0740","biotype":"protein_coding","ncbi_id":"9886","summary":"The protein encoded by this gene belongs to the Rho family of the small GTPase superfamily. It contains a GTPase domain, a proline-rich region, a tandem of 2 BTB (broad complex, tramtrack, and bric-a-brac) domains, and a conserved C-terminal region. The protein plays a role in small GTPase-mediated signal transduction and the organization of the actin filament system. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":60869438,"end":61001440,"strand":-1,"description":"Rho related BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18738]"}, {"versioned_ensembl_gene_id":"ENSG00000139343.10","gene_symbol":"SNRPF","gene_name":"small nuclear ribonucleoprotein polypeptide F [Source:HGNC Symbol;Acc:HGNC:11162]","synonyms":"Sm-F","biotype":"protein_coding","ncbi_id":"6636","summary":null,"start":95858928,"end":95903828,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide F [Source:HGNC Symbol;Acc:HGNC:11162]"}, {"versioned_ensembl_gene_id":"ENSG00000271190.1","gene_symbol":"RPP40P2","gene_name":"ribonuclease P/MRP subunit p40 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420608","summary":null,"start":59262680,"end":59263391,"strand":1,"description":"ribonuclease P/MRP subunit p40 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39770]"}, {"versioned_ensembl_gene_id":"ENSG00000237599.9","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"D6S217E,RING11,ABCB3,PSF2","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32855328,"end":32872254,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000023041.11","gene_symbol":"ZDHHC6","gene_name":"zinc finger DHHC-type containing 6 [Source:HGNC Symbol;Acc:HGNC:19160]","synonyms":"FLJ21952,ZNF376","biotype":"protein_coding","ncbi_id":"64429","summary":null,"start":112424428,"end":112446917,"strand":-1,"description":"zinc finger DHHC-type containing 6 [Source:HGNC Symbol;Acc:HGNC:19160]"}, {"versioned_ensembl_gene_id":"ENSG00000108774.14","gene_symbol":"RAB5C","gene_name":"RAB5C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9785]","synonyms":"RABL,RAB5CL","biotype":"protein_coding","ncbi_id":"5878","summary":"Members of the Rab protein family are small GTPases of the Ras superfamily that are thought to ensure fidelity in the process of docking and/or fusion of vesicles with their correct acceptor compartment (Han et al., 1996 [PubMed 8646882]).[supplied by OMIM, Nov 2010]","start":42124976,"end":42155044,"strand":-1,"description":"RAB5C, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9785]"}, {"versioned_ensembl_gene_id":"ENSG00000206454.12","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"Oct4,OCT3,OTF3,MGC22487","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31156777,"end":31163150,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000262983.1","gene_symbol":"AF001550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21194847,"end":21205977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278755.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769814,"end":54784135,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000251342.1","gene_symbol":"AC026774.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76078666,"end":76079763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236587.1","gene_symbol":"AL662849.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31981170,"end":31984699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249604.1","gene_symbol":"AC096564.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107936031,"end":107941255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257541.1","gene_symbol":"LINC02403","gene_name":"long intergenic non-protein coding RNA 2403 [Source:HGNC Symbol;Acc:HGNC:53330]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369785","summary":null,"start":58087892,"end":58093362,"strand":1,"description":"long intergenic non-protein coding RNA 2403 [Source:HGNC Symbol;Acc:HGNC:53330]"}, {"versioned_ensembl_gene_id":"ENSG00000248554.1","gene_symbol":"AC114956.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43511058,"end":43521811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277439.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55021820,"end":55046379,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000188215.9","gene_symbol":"DCUN1D3","gene_name":"defective in cullin neddylation 1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28734]","synonyms":"SCCRO3,MGC48972,FLJ41725,DKFZp686O0290","biotype":"protein_coding","ncbi_id":"123879","summary":null,"start":20854925,"end":20900384,"strand":-1,"description":"defective in cullin neddylation 1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28734]"}, {"versioned_ensembl_gene_id":"ENSG00000231183.3","gene_symbol":"AC007003.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":76902491,"end":76919191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134533.6","gene_symbol":"RERG","gene_name":"RAS like estrogen regulated growth inhibitor [Source:HGNC Symbol;Acc:HGNC:15980]","synonyms":"MGC15754","biotype":"protein_coding","ncbi_id":"85004","summary":"RERG, a member of the RAS superfamily of GTPases, inhibits cell proliferation and tumor formation (Finlin et al., 2001 [PubMed 11533059]).[supplied by OMIM, Mar 2009]","start":15107783,"end":15348675,"strand":-1,"description":"RAS like estrogen regulated growth inhibitor [Source:HGNC Symbol;Acc:HGNC:15980]"}, {"versioned_ensembl_gene_id":"ENSG00000214243.3","gene_symbol":"AC004980.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76650401,"end":76650897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274955.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803541,"end":54814525,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000158163.14","gene_symbol":"DZIP1L","gene_name":"DAZ interacting zinc finger protein 1 like [Source:HGNC Symbol;Acc:HGNC:26551]","synonyms":"DZIP2,FLJ32844","biotype":"protein_coding","ncbi_id":"199221","summary":null,"start":138061990,"end":138115818,"strand":-1,"description":"DAZ interacting zinc finger protein 1 like [Source:HGNC Symbol;Acc:HGNC:26551]"}, {"versioned_ensembl_gene_id":"ENSG00000240002.1","gene_symbol":"YBX1P3","gene_name":"Y-box binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42424]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861556","summary":null,"start":114930541,"end":114931449,"strand":1,"description":"Y-box binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42424]"}, {"versioned_ensembl_gene_id":"ENSG00000258453.3","gene_symbol":"OR11H2","gene_name":"olfactory receptor family 11 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:14716]","synonyms":"OR11H8P,OR11H2P,C14orf15","biotype":"protein_coding","ncbi_id":"79334","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19712904,"end":19714332,"strand":-1,"description":"olfactory receptor family 11 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:14716]"}, {"versioned_ensembl_gene_id":"ENSG00000236777.1","gene_symbol":"AL157831.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22163092,"end":22164306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135045.6","gene_symbol":"C9orf40","gene_name":"chromosome 9 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:23433]","synonyms":"FLJ10110","biotype":"protein_coding","ncbi_id":"55071","summary":null,"start":74946581,"end":74952886,"strand":-1,"description":"chromosome 9 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:23433]"}, {"versioned_ensembl_gene_id":"ENSG00000265489.1","gene_symbol":"AC005358.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12760140,"end":12790242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277408.1","gene_symbol":"Z99129.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122531123,"end":122531436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186007.9","gene_symbol":"LEMD1","gene_name":"LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18725]","synonyms":"LEMP-1,CT50","biotype":"protein_coding","ncbi_id":"93273","summary":null,"start":205381378,"end":205457091,"strand":-1,"description":"LEM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18725]"}, {"versioned_ensembl_gene_id":"ENSG00000225715.1","gene_symbol":"AL512504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80709928,"end":80710705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236552.2","gene_symbol":"RPL13AP5","gene_name":"ribosomal protein L13a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23736]","synonyms":"bA196N24.2","biotype":"processed_pseudogene","ncbi_id":"728658","summary":null,"start":96750288,"end":96750899,"strand":1,"description":"ribosomal protein L13a pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23736]"}, {"versioned_ensembl_gene_id":"ENSG00000274166.2","gene_symbol":"GOLGA6L10","gene_name":"golgin A6 family-like 10 [Source:HGNC Symbol;Acc:HGNC:37228]","synonyms":"GOLGA6L18,GOLGA6L18","biotype":"protein_coding","ncbi_id":"647042","summary":null,"start":82418974,"end":82428498,"strand":-1,"description":"golgin A6 family-like 10 [Source:HGNC Symbol;Acc:HGNC:37228]"}, {"versioned_ensembl_gene_id":"ENSG00000279948.1","gene_symbol":"AC008895.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46946535,"end":46949156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279394.1","gene_symbol":"AC015871.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79875920,"end":79878179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000025156.12","gene_symbol":"HSF2","gene_name":"heat shock transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:5225]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3298","summary":"The protein encoded by this gene belongs to the HSF family of transcription factors that bind specifically to the heat-shock promoter element and activate transcription. Heat shock transcription factors activate heat-shock response genes under conditions of heat or other stresses. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":122399546,"end":122433119,"strand":1,"description":"heat shock transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:5225]"}, {"versioned_ensembl_gene_id":"ENSG00000266065.1","gene_symbol":"AP005202.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6493420,"end":6495668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183340.6","gene_symbol":"JRKL","gene_name":"JRK like [Source:HGNC Symbol;Acc:HGNC:6200]","synonyms":"HHMJG","biotype":"protein_coding","ncbi_id":"8690","summary":"The function of this gene has not yet been defined, however, the encoded protein shares similarity with the human (41% identical) and mouse (34% identical) jerky gene products. This protein may act as a nuclear regulatory protein. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]","start":96389989,"end":96507574,"strand":1,"description":"JRK like [Source:HGNC Symbol;Acc:HGNC:6200]"}, {"versioned_ensembl_gene_id":"ENSG00000282292.1","gene_symbol":"IGHVII-40-1","gene_name":"immunoglobulin heavy variable (II)-40-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5679]","synonyms":"IGHV(II)-40-1","biotype":"IG_V_pseudogene","ncbi_id":"28368","summary":null,"start":106465631,"end":106465688,"strand":-1,"description":"immunoglobulin heavy variable (II)-40-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5679]"}, {"versioned_ensembl_gene_id":"ENSG00000173572.11","gene_symbol":"NLRP13","gene_name":"NLR family pyrin domain containing 13 [Source:HGNC Symbol;Acc:HGNC:22937]","synonyms":"PAN13,NOD14,NALP13,CLR19.7","biotype":"protein_coding","ncbi_id":"126204","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":55891699,"end":55932336,"strand":-1,"description":"NLR family pyrin domain containing 13 [Source:HGNC Symbol;Acc:HGNC:22937]"}, {"versioned_ensembl_gene_id":"ENSG00000282425.1","gene_symbol":"IGHV3-38","gene_name":"immunoglobulin heavy variable 3-38 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5601]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28429","summary":null,"start":106435173,"end":106435702,"strand":-1,"description":"immunoglobulin heavy variable 3-38 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5601]"}, {"versioned_ensembl_gene_id":"ENSG00000177707.10","gene_symbol":"NECTIN3","gene_name":"nectin cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:17664]","synonyms":"PPR3,nectin-3,DKFZP566B0846,CDw113,CD113,PVRR3,PVRL3","biotype":"protein_coding","ncbi_id":"25945","summary":"This gene encodes a member of the nectin family of proteins, which function as adhesion molecules at adherens junctions. This family member interacts with other nectin-like proteins and with afadin, a filamentous actin-binding protein involved in the regulation of directional motility, cell proliferation and survival. This gene plays a role in ocular development involving the ciliary body. Mutations in this gene are believed to result in congenital ocular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":111070071,"end":111275563,"strand":1,"description":"nectin cell adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:17664]"}, {"versioned_ensembl_gene_id":"ENSG00000248915.2","gene_symbol":"ACTR6P1","gene_name":"ACTR6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44210]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421495","summary":null,"start":106836498,"end":106837601,"strand":-1,"description":"ACTR6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44210]"}, {"versioned_ensembl_gene_id":"ENSG00000110060.8","gene_symbol":"PUS3","gene_name":"pseudouridylate synthase 3 [Source:HGNC Symbol;Acc:HGNC:25461]","synonyms":"FKSG32","biotype":"protein_coding","ncbi_id":"83480","summary":"The protein encoded by this gene catalyzes the formation of tRNA pseudouridine from tRNA uridine at position 39 in the anticodon stem and loop of transfer RNAs. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":125893485,"end":125903221,"strand":-1,"description":"pseudouridylate synthase 3 [Source:HGNC Symbol;Acc:HGNC:25461]"}, {"versioned_ensembl_gene_id":"ENSG00000259229.2","gene_symbol":"AC026826.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79758549,"end":79758762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225156.2","gene_symbol":"AC012354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44954664,"end":44968762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180537.12","gene_symbol":"RNF182","gene_name":"ring finger protein 182 [Source:HGNC Symbol;Acc:HGNC:28522]","synonyms":"MGC33993","biotype":"protein_coding","ncbi_id":"221687","summary":null,"start":13924446,"end":13980302,"strand":1,"description":"ring finger protein 182 [Source:HGNC Symbol;Acc:HGNC:28522]"}, {"versioned_ensembl_gene_id":"ENSG00000155629.14","gene_symbol":"PIK3AP1","gene_name":"phosphoinositide-3-kinase adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:30034]","synonyms":"FLJ35564,BCAP","biotype":"protein_coding","ncbi_id":"118788","summary":null,"start":96593312,"end":96720514,"strand":-1,"description":"phosphoinositide-3-kinase adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:30034]"}, {"versioned_ensembl_gene_id":"ENSG00000185885.15","gene_symbol":"IFITM1","gene_name":"interferon induced transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:5412]","synonyms":"IFI17,CD225,9-27","biotype":"protein_coding","ncbi_id":"8519","summary":null,"start":313506,"end":315272,"strand":1,"description":"interferon induced transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:5412]"}, {"versioned_ensembl_gene_id":"ENSG00000206406.9","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb1,Ckb2","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31655467,"end":31663777,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000275737.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"nkat5,183ActI,CD158J,cl-49","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738502,"end":54752797,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000243886.1","gene_symbol":"AC117440.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137535572,"end":137536142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217239.3","gene_symbol":"AL136968.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5788346,"end":5788699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147202.17","gene_symbol":"DIAPH2","gene_name":"diaphanous related formin 2 [Source:HGNC Symbol;Acc:HGNC:2877]","synonyms":"POF2,POF,DIA2,DIA","biotype":"protein_coding","ncbi_id":"1730","summary":"The product of this gene belongs to the diaphanous subfamily of the formin homology family of proteins. This gene may play a role in the development and normal function of the ovaries. Defects in this gene have been linked to premature ovarian failure 2. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":96684663,"end":97604997,"strand":1,"description":"diaphanous related formin 2 [Source:HGNC Symbol;Acc:HGNC:2877]"}, {"versioned_ensembl_gene_id":"ENSG00000236928.3","gene_symbol":"AC008267.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66434634,"end":66435154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111732.10","gene_symbol":"AICDA","gene_name":"activation induced cytidine deaminase [Source:HGNC Symbol;Acc:HGNC:13203]","synonyms":"HIGM2,CDA2,ARP2,AID","biotype":"protein_coding","ncbi_id":"57379","summary":"This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. AICDA is specifically expressed and active in germinal center-like B cells. In the germinal center, AICDA is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. An epigenetic role in neoplastic transformation and lymphoma progression has been experimentally ascribed to AICDA using mouse models. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Jul 2020]","start":8602166,"end":8612871,"strand":-1,"description":"activation induced cytidine deaminase [Source:HGNC Symbol;Acc:HGNC:13203]"}, {"versioned_ensembl_gene_id":"ENSG00000215458.8","gene_symbol":"AATBC","gene_name":"apoptosis associated transcript in bladder cancer [Source:HGNC Symbol;Acc:HGNC:51526]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"284837","summary":null,"start":43805758,"end":43812567,"strand":-1,"description":"apoptosis associated transcript in bladder cancer [Source:HGNC Symbol;Acc:HGNC:51526]"}, {"versioned_ensembl_gene_id":"ENSG00000282777.1","gene_symbol":"IGHV3-30","gene_name":"immunoglobulin heavy variable 3-30 [Source:HGNC Symbol;Acc:HGNC:5591]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28439","summary":null,"start":106335853,"end":106336384,"strand":-1,"description":"immunoglobulin heavy variable 3-30 [Source:HGNC Symbol;Acc:HGNC:5591]"}, {"versioned_ensembl_gene_id":"ENSG00000225791.6","gene_symbol":"TRAM2-AS1","gene_name":"TRAM2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48663]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401264","summary":null,"start":52577307,"end":52583993,"strand":1,"description":"TRAM2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48663]"}, {"versioned_ensembl_gene_id":"ENSG00000244196.1","gene_symbol":"PPIAP15","gene_name":"peptidylprolyl isomerase A pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:9268]","synonyms":"PPIP5","biotype":"processed_pseudogene","ncbi_id":"5487","summary":null,"start":109471329,"end":109471812,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:9268]"}, {"versioned_ensembl_gene_id":"ENSG00000241128.2","gene_symbol":"OR14A2","gene_name":"olfactory receptor family 14 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15024]","synonyms":"OR5AX1P,OR5AX1","biotype":"protein_coding","ncbi_id":"388761","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247722957,"end":247724043,"strand":-1,"description":"olfactory receptor family 14 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15024]"}, {"versioned_ensembl_gene_id":"ENSG00000240167.1","gene_symbol":"RPS7P7","gene_name":"ribosomal protein S7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35690]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270870","summary":null,"start":42471810,"end":42472380,"strand":1,"description":"ribosomal protein S7 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35690]"}, {"versioned_ensembl_gene_id":"ENSG00000237398.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33131216,"end":33143325,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000236701.3","gene_symbol":"AL512594.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73648828,"end":73649839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232590.1","gene_symbol":"AL451127.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73573615,"end":73579498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226520.1","gene_symbol":"KIRREL1-IT1","gene_name":"KIRREL1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41412]","synonyms":"KIRREL-IT1","biotype":"sense_intronic","ncbi_id":"100505785","summary":null,"start":158025550,"end":158031166,"strand":1,"description":"KIRREL1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41412]"}, {"versioned_ensembl_gene_id":"ENSG00000166523.7","gene_symbol":"CLEC4E","gene_name":"C-type lectin domain family 4 member E [Source:HGNC Symbol;Acc:HGNC:14555]","synonyms":"mincle,CLECSF9","biotype":"protein_coding","ncbi_id":"26253","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type II transmembrane protein is a downstream target of CCAAT/enhancer binding protein (C/EBP), beta (CEBPB) and may play a role in inflammation. Alternative splice variants have been described but their full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":8533305,"end":8540963,"strand":-1,"description":"C-type lectin domain family 4 member E [Source:HGNC Symbol;Acc:HGNC:14555]"}, {"versioned_ensembl_gene_id":"ENSG00000275083.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850406,"end":54867200,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000253198.1","gene_symbol":"AC139365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43674270,"end":43674591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224281.4","gene_symbol":"SLC25A5-AS1","gene_name":"SLC25A5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43438]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100303728","summary":null,"start":119466034,"end":119469098,"strand":-1,"description":"SLC25A5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43438]"}, {"versioned_ensembl_gene_id":"ENSG00000237618.1","gene_symbol":"BTBD7P2","gene_name":"BTB domain containing 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44876]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420392","summary":null,"start":111322778,"end":111323397,"strand":1,"description":"BTB domain containing 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44876]"}, {"versioned_ensembl_gene_id":"ENSG00000174233.11","gene_symbol":"ADCY6","gene_name":"adenylate cyclase 6 [Source:HGNC Symbol;Acc:HGNC:237]","synonyms":"AC6","biotype":"protein_coding","ncbi_id":"112","summary":"This gene encodes a member of the adenylyl cyclase family of proteins, which are required for the synthesis of cyclic AMP. All members of this family have an intracellular N-terminus, a tandem repeat of six transmembrane domains separated by a cytoplasmic loop, and a C-terminal cytoplasmic domain. The two cytoplasmic regions bind ATP and form the catalytic core of the protein. Adenylyl cyclases are important effectors of transmembrane signaling pathways and are regulated by the activity of G protein coupled receptor signaling. This protein belongs to a small subclass of adenylyl cyclase proteins that are functionally related and are inhibited by protein kinase A, calcium ions and nitric oxide. A mutation in this gene is associated with arthrogryposis multiplex congenita. [provided by RefSeq, May 2015]","start":48766194,"end":48789037,"strand":-1,"description":"adenylate cyclase 6 [Source:HGNC Symbol;Acc:HGNC:237]"}, {"versioned_ensembl_gene_id":"ENSG00000225063.1","gene_symbol":"AC093422.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":205233821,"end":205236867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164808.16","gene_symbol":"SPIDR","gene_name":"scaffolding protein involved in DNA repair [Source:HGNC Symbol;Acc:HGNC:28971]","synonyms":"KIAA0146","biotype":"protein_coding","ncbi_id":"23514","summary":null,"start":47260575,"end":47736306,"strand":1,"description":"scaffolding protein involved in DNA repair [Source:HGNC Symbol;Acc:HGNC:28971]"}, {"versioned_ensembl_gene_id":"ENSG00000254384.1","gene_symbol":"MTND6P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39482]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481788","summary":null,"start":36278960,"end":36279483,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39482]"}, {"versioned_ensembl_gene_id":"ENSG00000276495.4","gene_symbol":"APBA2","gene_name":"amyloid beta precursor protein binding family A member 2 [Source:HGNC Symbol;Acc:HGNC:579]","synonyms":"X11L,MINT2,MGC:14091,LIN-10,HsT16821,D15S1518E","biotype":"protein_coding","ncbi_id":"321","summary":"The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a putative vesicular trafficking protein in the brain that can form a complex with the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. [provided by RefSeq, Jul 2017]","start":29060035,"end":29259075,"strand":1,"description":"amyloid beta precursor protein binding family A member 2 [Source:HGNC Symbol;Acc:HGNC:579]"}, {"versioned_ensembl_gene_id":"ENSG00000150893.10","gene_symbol":"FREM2","gene_name":"FRAS1 related extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:25396]","synonyms":"DKFZp686J0811","biotype":"protein_coding","ncbi_id":"341640","summary":"This gene encodes an integral membrane protein containing numerous CSPG (chondroitin sulfate proteoglycan element) repeats and Calx-beta domains. The encoded protein localizes to the basement membrane, forming a ternary complex that plays a role in epidermal-dermal interactions. This protein is important for the integrity of skin and renal epithelia. Mutations in this gene are associated with Fraser syndrome. [provided by RefSeq, Apr 2014]","start":38687129,"end":38887131,"strand":1,"description":"FRAS1 related extracellular matrix protein 2 [Source:HGNC Symbol;Acc:HGNC:25396]"}, {"versioned_ensembl_gene_id":"ENSG00000282438.1","gene_symbol":"AC001228.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2988746,"end":2990227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246115.3","gene_symbol":"SUPT4H1P2","gene_name":"SPT4 homolog, DSIF elongation factor subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50823]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287625","summary":null,"start":8512374,"end":8512726,"strand":-1,"description":"SPT4 homolog, DSIF elongation factor subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50823]"}, {"versioned_ensembl_gene_id":"ENSG00000164778.4","gene_symbol":"EN2","gene_name":"engrailed homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3343]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2020","summary":"Homeobox-containing genes are thought to have a role in controlling development. In Drosophila, the 'engrailed' (en) gene plays an important role during development in segmentation, where it is required for the formation of posterior compartments. Different mutations in the mouse homologs, En1 and En2, produced different developmental defects that frequently are lethal. The human engrailed homologs 1 and 2 encode homeodomain-containing proteins and have been implicated in the control of pattern formation during development of the central nervous system. [provided by RefSeq, Jul 2008]","start":155458129,"end":155464831,"strand":1,"description":"engrailed homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3343]"}, {"versioned_ensembl_gene_id":"ENSG00000224629.1","gene_symbol":"AC004975.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157263022,"end":157263229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253845.1","gene_symbol":"AC139365.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43672823,"end":43673075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225218.1","gene_symbol":"AP001628.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42831040,"end":42836477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214835.3","gene_symbol":"RPL23AP6","gene_name":"ribosomal protein L23a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16555]","synonyms":"dJ1068F16.1","biotype":"processed_pseudogene","ncbi_id":"128709","summary":null,"start":10349157,"end":10349628,"strand":-1,"description":"ribosomal protein L23a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16555]"}, {"versioned_ensembl_gene_id":"ENSG00000237572.1","gene_symbol":"AC092001.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63209219,"end":63211822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284294.1","gene_symbol":"AC007326.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18936411,"end":18947741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232765.6","gene_symbol":"AL158819.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55279839,"end":55288785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238248.4","gene_symbol":"CR933540.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32674660,"end":32675599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260170.1","gene_symbol":"AC090527.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":45587351,"end":45676314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261418.1","gene_symbol":"AC100756.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23430839,"end":23435212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237120.1","gene_symbol":"CR933540.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32677106,"end":32677513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172053.17","gene_symbol":"QARS","gene_name":"glutaminyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:9751]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5859","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. In metazoans, 9 aminoacyl-tRNA synthetases specific for glutamine (gln), glutamic acid (glu), and 7 other amino acids are associated within a multienzyme complex. Although present in eukaryotes, glutaminyl-tRNA synthetase (QARS) is absent from many prokaryotes, mitochondria, and chloroplasts, in which Gln-tRNA(Gln) is formed by transamidation of the misacylated Glu-tRNA(Gln). Glutaminyl-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":49095932,"end":49105135,"strand":-1,"description":"glutaminyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:9751]"}, {"versioned_ensembl_gene_id":"ENSG00000282201.1","gene_symbol":"AL023881.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":424243,"end":424543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238232.1","gene_symbol":"AL356364.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219557192,"end":219557701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109272.3","gene_symbol":"PF4V1","gene_name":"platelet factor 4 variant 1 [Source:HGNC Symbol;Acc:HGNC:8862]","synonyms":"SCYB4V1,CXCL4V1,CXCL4L1","biotype":"protein_coding","ncbi_id":"5197","summary":"The protein encoded by this gene is a chemokine that is highly similar to platelet factor 4. The encoded protein displays a strong antiangiogenic function and is regulated by chemokine (C-X-C motif) receptor 3. This protein also impairs tumor growth and can protect against blood-retinal barrier breakdown in diabetes patients. [provided by RefSeq, Nov 2015]","start":73853189,"end":73854155,"strand":1,"description":"platelet factor 4 variant 1 [Source:HGNC Symbol;Acc:HGNC:8862]"}, {"versioned_ensembl_gene_id":"ENSG00000232542.1","gene_symbol":"DPYD-IT1","gene_name":"DPYD intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41326]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874267","summary":null,"start":97394154,"end":97420141,"strand":-1,"description":"DPYD intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41326]"}, {"versioned_ensembl_gene_id":"ENSG00000226075.2","gene_symbol":"PHKG1P1","gene_name":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33916]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643941","summary":null,"start":63233035,"end":63234245,"strand":-1,"description":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33916]"}, {"versioned_ensembl_gene_id":"ENSG00000101222.12","gene_symbol":"SPEF1","gene_name":"sperm flagellar 1 [Source:HGNC Symbol;Acc:HGNC:15874]","synonyms":"SPEF1A,DKFZP434I114,CLAMP,C20orf28","biotype":"protein_coding","ncbi_id":"25876","summary":null,"start":3777504,"end":3781448,"strand":-1,"description":"sperm flagellar 1 [Source:HGNC Symbol;Acc:HGNC:15874]"}, {"versioned_ensembl_gene_id":"ENSG00000255026.1","gene_symbol":"AC136475.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":287305,"end":288987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215817.5","gene_symbol":"ZC3H11B","gene_name":"zinc finger CCCH-type containing 11B pseudogene [Source:HGNC Symbol;Acc:HGNC:25659]","synonyms":"ZC3HDC11B","biotype":"protein_coding","ncbi_id":"643136","summary":null,"start":219608347,"end":219613145,"strand":-1,"description":"zinc finger CCCH-type containing 11B pseudogene [Source:HGNC Symbol;Acc:HGNC:25659]"}, {"versioned_ensembl_gene_id":"ENSG00000124549.14","gene_symbol":"BTN2A3P","gene_name":"butyrophilin subfamily 2 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:13229]","synonyms":"BTN2A3,BTN2.3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54718","summary":"The butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC)-associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30.2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single-copy BTN1A1 gene (MIM 601610) and the BTN2 (e.g., BTN2A3) and BTN3 (e.g., BNT3A1; MIM 613593) genes, which have undergone tandem duplication, resulting in 3 copies of each (summary by Smith et al., 2010 [PubMed 20208008]).[supplied by OMIM, Nov 2010]","start":26421391,"end":26432383,"strand":1,"description":"butyrophilin subfamily 2 member A3, pseudogene [Source:HGNC Symbol;Acc:HGNC:13229]"}, {"versioned_ensembl_gene_id":"ENSG00000203643.3","gene_symbol":"AC012456.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11721619,"end":11724222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196660.10","gene_symbol":"SLC30A10","gene_name":"solute carrier family 30 member 10 [Source:HGNC Symbol;Acc:HGNC:25355]","synonyms":"ZRC1,ZNT8,ZnT-10,DKFZp547M236","biotype":"protein_coding","ncbi_id":"55532","summary":"This gene is highly expressed in the liver and is inducible by manganese. Its protein product appears to be critical in maintaining manganese levels, and has higher specificity for manganese than zinc. Loss of function mutations appear to result in a pleomorphic phenotype, including dystonia and adult-onset parkinsonism. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]","start":219685427,"end":219958647,"strand":-1,"description":"solute carrier family 30 member 10 [Source:HGNC Symbol;Acc:HGNC:25355]"}, {"versioned_ensembl_gene_id":"ENSG00000204538.3","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31137536,"end":31139350,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000232130.1","gene_symbol":"AC092966.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":193144464,"end":193176864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134324.11","gene_symbol":"LPIN1","gene_name":"lipin 1 [Source:HGNC Symbol;Acc:HGNC:13345]","synonyms":"KIAA0188","biotype":"protein_coding","ncbi_id":"23175","summary":"This gene encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, acute recurrent rhabdomyolysis, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes. [provided by RefSeq, Mar 2017]","start":11677595,"end":11827409,"strand":1,"description":"lipin 1 [Source:HGNC Symbol;Acc:HGNC:13345]"}, {"versioned_ensembl_gene_id":"ENSG00000236229.1","gene_symbol":"VEZF1P1","gene_name":"vascular endothelial zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32320]","synonyms":"VEZF1L1,ZNF161L1","biotype":"processed_pseudogene","ncbi_id":"647319","summary":null,"start":193155456,"end":193157208,"strand":-1,"description":"vascular endothelial zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32320]"}, {"versioned_ensembl_gene_id":"ENSG00000180767.9","gene_symbol":"CHST13","gene_name":"carbohydrate sulfotransferase 13 [Source:HGNC Symbol;Acc:HGNC:21755]","synonyms":"C4ST3","biotype":"protein_coding","ncbi_id":"166012","summary":"The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to the C4 hydroxyl of beta-1,4-linked N-acetylgalactosamine (GalNAc) flanked by glucuronic acid residue in chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage and is distributed on the surfaces of many cells and extracellular matrices. [provided by RefSeq, Aug 2011]","start":126524283,"end":126543291,"strand":1,"description":"carbohydrate sulfotransferase 13 [Source:HGNC Symbol;Acc:HGNC:21755]"}, {"versioned_ensembl_gene_id":"ENSG00000231124.1","gene_symbol":"UBE2V1P11","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:44896]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723977","summary":null,"start":201824548,"end":201824832,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:44896]"}, {"versioned_ensembl_gene_id":"ENSG00000204539.3","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31115090,"end":31120446,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000277963.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000136273.11","gene_symbol":"HUS1","gene_name":"HUS1 checkpoint clamp component [Source:HGNC Symbol;Acc:HGNC:5309]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3364","summary":"The protein encoded by this gene is a component of an evolutionarily conserved, genotoxin-activated checkpoint complex that is involved in the cell cycle arrest in response to DNA damage. This protein forms a heterotrimeric complex with checkpoint proteins RAD9 and RAD1. In response to DNA damage, the trimeric complex interacts with another protein complex consisting of checkpoint protein RAD17 and four small subunits of the replication factor C (RFC), which loads the combined complex onto the chromatin. The DNA damage induced chromatin binding has been shown to depend on the activation of the checkpoint kinase ATM, and is thought to be an early checkpoint signaling event. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2011]","start":47695730,"end":47979581,"strand":-1,"description":"HUS1 checkpoint clamp component [Source:HGNC Symbol;Acc:HGNC:5309]"}, {"versioned_ensembl_gene_id":"ENSG00000280110.1","gene_symbol":"AC087893.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108778912,"end":108779166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269881.1","gene_symbol":"AC004754.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":249547,"end":269943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274598.1","gene_symbol":"AC087893.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":108833721,"end":108834384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232266.1","gene_symbol":"CR936237.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31950783,"end":31951076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203364.2","gene_symbol":"AL390760.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93147040,"end":93148556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204540.10","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"SEEK1,C6orf16","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31114750,"end":31140092,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000249960.2","gene_symbol":"AC067942.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82571137,"end":82571814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084112.14","gene_symbol":"SSH1","gene_name":"slingshot protein phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:30579]","synonyms":"KIAA1298","biotype":"protein_coding","ncbi_id":"54434","summary":"The protein encoded by this gene belongs to the slingshot homolog (SSH) family of phosphatases, which regulate actin filament dynamics. The SSH proteins dephosphorylate and activate the actin binding/depolymerizing factor cofilin, which subsequently binds to actin filaments and stimulates their disassembly. Cofilin is inactivated by kinases such as LIM domain kinase-1 (LIMK1), which may also be dephosphorylated and inactivated by SSH proteins. The SSH family thus appears to play a role in actin dynamics by reactivating cofilin proteins. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":108778192,"end":108857590,"strand":-1,"description":"slingshot protein phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:30579]"}, {"versioned_ensembl_gene_id":"ENSG00000248113.2","gene_symbol":"AC067942.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82580117,"end":82581384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242173.8","gene_symbol":"ARHGDIG","gene_name":"Rho GDP dissociation inhibitor gamma [Source:HGNC Symbol;Acc:HGNC:680]","synonyms":"RHOGDI-3","biotype":"protein_coding","ncbi_id":"398","summary":"The GDP-dissociation inhibitors (GDIs) play a primary role in modulating the activation of GTPases by inhibiting the exchange of GDP for GTP. See ARHGDIB (MIM 602843).[supplied by OMIM, Nov 2010]","start":268727,"end":283010,"strand":1,"description":"Rho GDP dissociation inhibitor gamma [Source:HGNC Symbol;Acc:HGNC:680]"}, {"versioned_ensembl_gene_id":"ENSG00000243974.1","gene_symbol":"VTI1BP1","gene_name":"vesicle transport through interaction with t-SNAREs 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391559","summary":null,"start":100225374,"end":100226073,"strand":1,"description":"vesicle transport through interaction with t-SNAREs 1B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43727]"}, {"versioned_ensembl_gene_id":"ENSG00000232045.7","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"C6orf30,G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31946781,"end":31964716,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000284664.1","gene_symbol":"AL161756.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64349677,"end":64352284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224796.1","gene_symbol":"AL645931.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33079451,"end":33079860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271511.1","gene_symbol":"AL161756.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64361392,"end":64361637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180697.8","gene_symbol":"C3orf22","gene_name":"chromosome 3 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:28534]","synonyms":"MGC34728","biotype":"protein_coding","ncbi_id":"152065","summary":null,"start":126526999,"end":126558965,"strand":-1,"description":"chromosome 3 open reading frame 22 [Source:HGNC Symbol;Acc:HGNC:28534]"}, {"versioned_ensembl_gene_id":"ENSG00000234911.2","gene_symbol":"TEX21P","gene_name":"testis expressed 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:35455]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"441687","summary":null,"start":64341673,"end":64387986,"strand":-1,"description":"testis expressed 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:35455]"}, {"versioned_ensembl_gene_id":"ENSG00000151092.16","gene_symbol":"NGLY1","gene_name":"N-glycanase 1 [Source:HGNC Symbol;Acc:HGNC:17646]","synonyms":"PNG1,FLJ11005","biotype":"protein_coding","ncbi_id":"55768","summary":"This gene encodes an enzyme that catalyzes hydrolysis of an N(4)-(acetyl-beta-D-glucosaminyl) asparagine residue to N-acetyl-beta-D-glucosaminylamine and a peptide containing an aspartate residue. The encoded enzyme may play a role in the proteasome-mediated degradation of misfolded glycoproteins. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2009]","start":25718944,"end":25790039,"strand":-1,"description":"N-glycanase 1 [Source:HGNC Symbol;Acc:HGNC:17646]"}, {"versioned_ensembl_gene_id":"ENSG00000198805.11","gene_symbol":"PNP","gene_name":"purine nucleoside phosphorylase [Source:HGNC Symbol;Acc:HGNC:7892]","synonyms":"PUNP,NP","biotype":"protein_coding","ncbi_id":"4860","summary":"This gene encodes an enzyme which reversibly catalyzes the phosphorolysis of purine nucleosides. The enzyme is trimeric, containing three identical subunits. Mutations which result in nucleoside phosphorylase deficiency result in defective T-cell (cell-mediated) immunity but can also affect B-cell immunity and antibody responses. Neurologic disorders may also be apparent in patients with immune defects. A known polymorphism at aa position 51 that does not affect enzyme activity has been described. A pseudogene has been identified on chromosome 2. [provided by RefSeq, Jul 2008]","start":20468954,"end":20477094,"strand":1,"description":"purine nucleoside phosphorylase [Source:HGNC Symbol;Acc:HGNC:7892]"}, {"versioned_ensembl_gene_id":"ENSG00000135046.13","gene_symbol":"ANXA1","gene_name":"annexin A1 [Source:HGNC Symbol;Acc:HGNC:533]","synonyms":"LPC1,ANX1","biotype":"protein_coding","ncbi_id":"301","summary":"This gene encodes a membrane-localized protein that binds phospholipids. This protein inhibits phospholipase A2 and has anti-inflammatory activity. Loss of function or expression of this gene has been detected in multiple tumors. [provided by RefSeq, Dec 2014]","start":73151757,"end":73170393,"strand":1,"description":"annexin A1 [Source:HGNC Symbol;Acc:HGNC:533]"}, {"versioned_ensembl_gene_id":"ENSG00000235763.1","gene_symbol":"SNRPGP5","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39324]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874418","summary":null,"start":13104574,"end":13104793,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39324]"}, {"versioned_ensembl_gene_id":"ENSG00000186283.13","gene_symbol":"TOR3A","gene_name":"torsin family 3 member A [Source:HGNC Symbol;Acc:HGNC:11997]","synonyms":"FLJ22345,ADIR2,ADIR","biotype":"protein_coding","ncbi_id":"64222","summary":null,"start":179081377,"end":179098023,"strand":1,"description":"torsin family 3 member A [Source:HGNC Symbol;Acc:HGNC:11997]"}, {"versioned_ensembl_gene_id":"ENSG00000225251.1","gene_symbol":"RPL5P25","gene_name":"ribosomal protein L5 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271204","summary":null,"start":13057902,"end":13058676,"strand":-1,"description":"ribosomal protein L5 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:35493]"}, {"versioned_ensembl_gene_id":"ENSG00000169891.17","gene_symbol":"REPS2","gene_name":"RALBP1 associated Eps domain containing 2 [Source:HGNC Symbol;Acc:HGNC:9963]","synonyms":"POB1","biotype":"protein_coding","ncbi_id":"9185","summary":"The product of this gene is part of a protein complex that regulates the endocytosis of growth factor receptors. The encoded protein directly interacts with a GTPase activating protein that functions downstream of the small G protein Ral. Its expression can negatively affect receptor internalization and inhibit growth factor signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":16946691,"end":17153280,"strand":1,"description":"RALBP1 associated Eps domain containing 2 [Source:HGNC Symbol;Acc:HGNC:9963]"}, {"versioned_ensembl_gene_id":"ENSG00000280850.1","gene_symbol":"AL121956.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166275462,"end":166277077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256967.1","gene_symbol":"AC018653.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7129079,"end":7131198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227531.1","gene_symbol":"AL162414.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111139246,"end":111284836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225443.1","gene_symbol":"AC004938.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44511025,"end":44511332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120860.10","gene_symbol":"WASHC3","gene_name":"WASH complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24256]","synonyms":"CGI-116,CCDC53","biotype":"protein_coding","ncbi_id":"51019","summary":null,"start":102012927,"end":102062149,"strand":-1,"description":"WASH complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:24256]"}, {"versioned_ensembl_gene_id":"ENSG00000253524.1","gene_symbol":"AC124290.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36004316,"end":36095046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198488.10","gene_symbol":"B3GNT6","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:24141]","synonyms":"B3Gn-T6","biotype":"protein_coding","ncbi_id":"192134","summary":"The protein encoded by this gene is a beta-1,3-N-acetylglucosaminyltransferase that adds an N-acetylglucosamine moiety to N-acetylgalactosamine-modified serine or threonine. The encoded enzyme is responsible for creating the core 3 structure of O-glycans, which are important components of mucin-type glycoproteins. [provided by RefSeq, Dec 2016]","start":77034398,"end":77041973,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:24141]"}, {"versioned_ensembl_gene_id":"ENSG00000198848.12","gene_symbol":"CES1","gene_name":"carboxylesterase 1 [Source:HGNC Symbol;Acc:HGNC:1863]","synonyms":"HMSE,CES2,CES1A2,CES1A1,CEH,SES1,HMSE1","biotype":"protein_coding","ncbi_id":"1066","summary":"This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This enzyme is the major liver enzyme and functions in liver drug clearance. Mutations of this gene cause carboxylesterase 1 deficiency. Three transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":55802851,"end":55833337,"strand":-1,"description":"carboxylesterase 1 [Source:HGNC Symbol;Acc:HGNC:1863]"}, {"versioned_ensembl_gene_id":"ENSG00000254309.1","gene_symbol":"AC124290.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36121398,"end":36121683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253504.1","gene_symbol":"MTCYBP19","gene_name":"mitochondrially encoded cytochrome b pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51971]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075127","summary":null,"start":36277763,"end":36278886,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:51971]"}, {"versioned_ensembl_gene_id":"ENSG00000151631.8","gene_symbol":"AKR1C6P","gene_name":"aldo-keto reductase family 1 member C6, pseudogene [Source:HGNC Symbol;Acc:HGNC:44680]","synonyms":"TAKR","biotype":"unprocessed_pseudogene","ncbi_id":"389932","summary":null,"start":4871901,"end":4891975,"strand":-1,"description":"aldo-keto reductase family 1 member C6, pseudogene [Source:HGNC Symbol;Acc:HGNC:44680]"}, {"versioned_ensembl_gene_id":"ENSG00000280294.1","gene_symbol":"AC011008.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10856085,"end":10859436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281609.1","gene_symbol":"AC109471.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125376828,"end":125377439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275563.1","gene_symbol":"AL929601.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18977180,"end":18980742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253685.1","gene_symbol":"MTND5P41","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:51972]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075309","summary":null,"start":36279491,"end":36279696,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:51972]"}, {"versioned_ensembl_gene_id":"ENSG00000130669.17","gene_symbol":"PAK4","gene_name":"p21 (RAC1) activated kinase 4 [Source:HGNC Symbol;Acc:HGNC:16059]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10298","summary":"PAK proteins, a family of serine/threonine p21-activating kinases, include PAK1, PAK2, PAK3 and PAK4. PAK proteins are critical effectors that link Rho GTPases to cytoskeleton reorganization and nuclear signaling. They serve as targets for the small GTP binding proteins Cdc42 and Rac and have been implicated in a wide range of biological activities. PAK4 interacts specifically with the GTP-bound form of Cdc42Hs and weakly activates the JNK family of MAP kinases. PAK4 is a mediator of filopodia formation and may play a role in the reorganization of the actin cytoskeleton. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":39125770,"end":39182816,"strand":1,"description":"p21 (RAC1) activated kinase 4 [Source:HGNC Symbol;Acc:HGNC:16059]"}, {"versioned_ensembl_gene_id":"ENSG00000253610.1","gene_symbol":"AP006245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36308245,"end":36308364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254320.1","gene_symbol":"AP006245.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36321039,"end":36321404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277000.1","gene_symbol":"DUSP12P1","gene_name":"dual specificity phosphatase 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49059]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420473","summary":null,"start":100221268,"end":100223858,"strand":-1,"description":"dual specificity phosphatase 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49059]"}, {"versioned_ensembl_gene_id":"ENSG00000253363.5","gene_symbol":"AC090809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36537391,"end":36779164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244708.1","gene_symbol":"RPL23P10","gene_name":"ribosomal protein L23 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36177]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270962","summary":null,"start":36581180,"end":36581591,"strand":-1,"description":"ribosomal protein L23 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36177]"}, {"versioned_ensembl_gene_id":"ENSG00000253695.1","gene_symbol":"AC011008.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10840576,"end":10846501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182180.13","gene_symbol":"MRPS16","gene_name":"mitochondrial ribosomal protein S16 [Source:HGNC Symbol;Acc:HGNC:14048]","synonyms":"CGI-132","biotype":"protein_coding","ncbi_id":"51021","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S16P family. The encoded protein is one of the most highly conserved ribosomal proteins between mammalian and yeast mitochondria. Three pseudogenes (located at 8q21.3, 20q13.32, 22q12-q13.1) for this gene have been described. [provided by RefSeq, Jul 2008]","start":73248843,"end":73252693,"strand":-1,"description":"mitochondrial ribosomal protein S16 [Source:HGNC Symbol;Acc:HGNC:14048]"}, {"versioned_ensembl_gene_id":"ENSG00000261738.6","gene_symbol":"MIR3976HG","gene_name":"MIR3976 host gene [Source:HGNC Symbol;Acc:HGNC:51104]","synonyms":"LINC01469","biotype":"lincRNA","ncbi_id":"645355","summary":null,"start":5748819,"end":5876328,"strand":1,"description":"MIR3976 host gene [Source:HGNC Symbol;Acc:HGNC:51104]"}, {"versioned_ensembl_gene_id":"ENSG00000176381.5","gene_symbol":"PRR18","gene_name":"proline rich 18 [Source:HGNC Symbol;Acc:HGNC:28574]","synonyms":"MGC35308","biotype":"protein_coding","ncbi_id":"285800","summary":null,"start":166305300,"end":166308448,"strand":-1,"description":"proline rich 18 [Source:HGNC Symbol;Acc:HGNC:28574]"}, {"versioned_ensembl_gene_id":"ENSG00000281490.1","gene_symbol":"CICP14","gene_name":"capicua transcriptional repressor pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130600","summary":null,"start":128655962,"end":128658791,"strand":-1,"description":"capicua transcriptional repressor pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38542]"}, {"versioned_ensembl_gene_id":"ENSG00000282460.1","gene_symbol":"AC099689.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79088732,"end":79090033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282266.2","gene_symbol":"ATP9B","gene_name":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]","synonyms":"ATPIIB","biotype":"protein_coding","ncbi_id":"374868","summary":null,"start":79072883,"end":79091276,"strand":1,"description":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]"}, {"versioned_ensembl_gene_id":"ENSG00000204371.11","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"C6orf30,G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31879759,"end":31897687,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000281036.1","gene_symbol":"AC109471.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125325350,"end":125367734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171133.3","gene_symbol":"OR2K2","gene_name":"olfactory receptor family 2 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:8264]","synonyms":"OR2AR1P,HTPCRH06,HSHTPCRH06","biotype":"protein_coding","ncbi_id":"26248","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":111327483,"end":111330183,"strand":-1,"description":"olfactory receptor family 2 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:8264]"}, {"versioned_ensembl_gene_id":"ENSG00000076344.15","gene_symbol":"RGS11","gene_name":"regulator of G protein signaling 11 [Source:HGNC Symbol;Acc:HGNC:9993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8786","summary":"The protein encoded by this gene belongs to the RGS (regulator of G protein signaling) family. Members of the RGS family act as GTPase-activating proteins on the alpha subunits of heterotrimeric, signal-transducing G proteins. This protein inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound form. Alternative splicing occurs at this locus and four transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Nov 2013]","start":268301,"end":275980,"strand":-1,"description":"regulator of G protein signaling 11 [Source:HGNC Symbol;Acc:HGNC:9993]"}, {"versioned_ensembl_gene_id":"ENSG00000224151.1","gene_symbol":"USP9YP28","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:38764]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107080622","summary":null,"start":18833002,"end":18839313,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:38764]"}, {"versioned_ensembl_gene_id":"ENSG00000153406.13","gene_symbol":"NMRAL1","gene_name":"NmrA like redox sensor 1 [Source:HGNC Symbol;Acc:HGNC:24987]","synonyms":"SDR48A1,HSCARG,FLJ25918","biotype":"protein_coding","ncbi_id":"57407","summary":"This gene encodes an NADPH sensor protein that preferentially binds to NADPH. The encoded protein also negatively regulates the activity of NF-kappaB in a ubiquitylation-dependent manner. It plays a key role in cellular antiviral response by negatively regulating the interferon response factor 3-mediated expression of interferon beta. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":4461680,"end":4495763,"strand":-1,"description":"NmrA like redox sensor 1 [Source:HGNC Symbol;Acc:HGNC:24987]"}, {"versioned_ensembl_gene_id":"ENSG00000222036.7","gene_symbol":"POTEM","gene_name":"POTE ankyrin domain family member M [Source:HGNC Symbol;Acc:HGNC:37096]","synonyms":"POTE14beta,P704P,ACT","biotype":"protein_coding","ncbi_id":"641455","summary":null,"start":18967434,"end":18999012,"strand":1,"description":"POTE ankyrin domain family member M [Source:HGNC Symbol;Acc:HGNC:37096]"}, {"versioned_ensembl_gene_id":"ENSG00000271553.1","gene_symbol":"AC018638.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128667043,"end":128668156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241185.2","gene_symbol":"AC005410.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":11998353,"end":12021508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181652.19","gene_symbol":"ATG9B","gene_name":"autophagy related 9B [Source:HGNC Symbol;Acc:HGNC:21899]","synonyms":"SONE,NOS3AS,FLJ14885,APG9L2","biotype":"protein_coding","ncbi_id":"285973","summary":"This gene functions in the regulation of autophagy, a lysosomal degradation pathway. This gene also functions as an antisense transcript in the posttranscriptional regulation of the endothelial nitric oxide synthase 3 gene, which has 3' overlap with this gene on the opposite strand. Mutations in this gene and disruption of the autophagy process have been associated with multiple cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":151012209,"end":151024499,"strand":-1,"description":"autophagy related 9B [Source:HGNC Symbol;Acc:HGNC:21899]"}, {"versioned_ensembl_gene_id":"ENSG00000166887.15","gene_symbol":"VPS39","gene_name":"VPS39, HOPS complex subunit [Source:HGNC Symbol;Acc:HGNC:20593]","synonyms":"VAM6,KIAA0770","biotype":"protein_coding","ncbi_id":"23339","summary":"This gene encodes a protein that may promote clustering and fusion of late endosomes and lysosomes. The protein may also act as an adaptor protein that modulates the transforming growth factor-beta response by coupling the transforming growth factor-beta receptor complex to the Smad pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":42158701,"end":42208316,"strand":-1,"description":"VPS39, HOPS complex subunit [Source:HGNC Symbol;Acc:HGNC:20593]"}, {"versioned_ensembl_gene_id":"ENSG00000243479.3","gene_symbol":"MNX1-AS1","gene_name":"MNX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48954]","synonyms":"CCAT5,LOC645249","biotype":"lincRNA","ncbi_id":"645249","summary":null,"start":157010805,"end":157016426,"strand":1,"description":"MNX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48954]"}, {"versioned_ensembl_gene_id":"ENSG00000156042.17","gene_symbol":"CFAP70","gene_name":"cilia and flagella associated protein 70 [Source:HGNC Symbol;Acc:HGNC:30726]","synonyms":"TTC18,FLJ25765","biotype":"protein_coding","ncbi_id":"118491","summary":null,"start":73253759,"end":73358859,"strand":-1,"description":"cilia and flagella associated protein 70 [Source:HGNC Symbol;Acc:HGNC:30726]"}, {"versioned_ensembl_gene_id":"ENSG00000241493.1","gene_symbol":"AC018638.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128669087,"end":128669892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263648.1","gene_symbol":"AC005244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12115547,"end":12115885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236102.2","gene_symbol":"AC006967.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157057709,"end":157058514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229365.3","gene_symbol":"AC006967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157087955,"end":157088543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065559.14","gene_symbol":"MAP2K4","gene_name":"mitogen-activated protein kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6844]","synonyms":"SERK1,PRKMK4,MKK4,MEK4,JNKK1","biotype":"protein_coding","ncbi_id":"6416","summary":"This gene encodes a member of the mitogen-activated protein kinase (MAPK) family. Members of this family act as an integration point for multiple biochemical signals and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation, and development. They form a three-tiered signaling module composed of MAPKKKs, MAPKKs, and MAPKs. This protein is phosphorylated at serine and threonine residues by MAPKKKs and subsequently phosphorylates downstream MAPK targets at threonine and tyrosine residues. A similar protein in mouse has been reported to play a role in liver organogenesis. A pseudogene of this gene is located on the long arm of chromosome X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":12020824,"end":12143830,"strand":1,"description":"mitogen-activated protein kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6844]"}, {"versioned_ensembl_gene_id":"ENSG00000269446.2","gene_symbol":"AC006967.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157109980,"end":157111072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169962.4","gene_symbol":"TAS1R3","gene_name":"taste 1 receptor member 3 [Source:HGNC Symbol;Acc:HGNC:15661]","synonyms":"T1R3","biotype":"protein_coding","ncbi_id":"83756","summary":"The protein encoded by this gene is a G-protein coupled receptor involved in taste responses. The encoded protein can form a heterodimeric receptor with TAS1R1 to elicit the umami taste response, or it can bind with TAS1R2 to form a receptor for the sweet taste response. [provided by RefSeq, Nov 2015]","start":1331314,"end":1335306,"strand":1,"description":"taste 1 receptor member 3 [Source:HGNC Symbol;Acc:HGNC:15661]"}, {"versioned_ensembl_gene_id":"ENSG00000214322.3","gene_symbol":"CBX1P2","gene_name":"chromobox 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38656]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100147811","summary":null,"start":17099782,"end":17100239,"strand":-1,"description":"chromobox 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38656]"}, {"versioned_ensembl_gene_id":"ENSG00000163644.14","gene_symbol":"PPM1K","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1K [Source:HGNC Symbol;Acc:HGNC:25415]","synonyms":"PP2Ckappa,hPTMP,DKFZp761G058,BDP,PP2Cm","biotype":"protein_coding","ncbi_id":"152926","summary":"This gene encodes a member of the PPM family of Mn2+/Mg2+-dependent protein phosphatases. The encoded protein, essential for cell survival and development, is targeted to the mitochondria where it plays a key role in regulation of the mitochondrial permeability transition pore. [provided by RefSeq, Sep 2012]","start":88257620,"end":88284769,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1K [Source:HGNC Symbol;Acc:HGNC:25415]"}, {"versioned_ensembl_gene_id":"ENSG00000258908.1","gene_symbol":"AL355075.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20474789,"end":20477089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107404.19","gene_symbol":"DVL1","gene_name":"dishevelled segment polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:3084]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1855","summary":"DVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development. [provided by RefSeq, Jul 2008]","start":1335276,"end":1349350,"strand":-1,"description":"dishevelled segment polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:3084]"}, {"versioned_ensembl_gene_id":"ENSG00000276324.1","gene_symbol":"AC245128.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228498.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32987088,"end":32987162,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000282601.1","gene_symbol":"HOMER2P2","gene_name":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317769","summary":null,"start":106287582,"end":106288428,"strand":-1,"description":"homer scaffolding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20334]"}, {"versioned_ensembl_gene_id":"ENSG00000235425.2","gene_symbol":"RPS7P13","gene_name":"ribosomal protein S7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130435","summary":null,"start":95679130,"end":95679627,"strand":-1,"description":"ribosomal protein S7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:35756]"}, {"versioned_ensembl_gene_id":"ENSG00000282710.1","gene_symbol":"IGHV3-25","gene_name":"immunoglobulin heavy variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5589]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28441","summary":null,"start":106289800,"end":106290250,"strand":-1,"description":"immunoglobulin heavy variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5589]"}, {"versioned_ensembl_gene_id":"ENSG00000281926.1","gene_symbol":"IGHVIII-25-1","gene_name":"immunoglobulin heavy variable (III)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5697]","synonyms":"IGHV(III)-25-1","biotype":"IG_V_pseudogene","ncbi_id":"28348","summary":null,"start":106294339,"end":106294579,"strand":-1,"description":"immunoglobulin heavy variable (III)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5697]"}, {"versioned_ensembl_gene_id":"ENSG00000270583.1","gene_symbol":"AL365400.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95720243,"end":95721144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166321.13","gene_symbol":"NUDT13","gene_name":"nudix hydrolase 13 [Source:HGNC Symbol;Acc:HGNC:18827]","synonyms":"DKFZp586P2219","biotype":"protein_coding","ncbi_id":"25961","summary":null,"start":73110375,"end":73131828,"strand":1,"description":"nudix hydrolase 13 [Source:HGNC Symbol;Acc:HGNC:18827]"}, {"versioned_ensembl_gene_id":"ENSG00000235895.1","gene_symbol":"AC010154.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6492976,"end":6496757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171243.7","gene_symbol":"SOSTDC1","gene_name":"sclerostin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21748]","synonyms":"USAG1,DKFZp564D206,DAND7","biotype":"protein_coding","ncbi_id":"25928","summary":"This gene is a member of the sclerostin family and encodes an N-glycosylated, secreted protein with a C-terminal cystine knot-like domain. This protein functions as a bone morphogenetic protein (BMP) antagonist. Specifically, it directly associates with BMPs, prohibiting them from binding their receptors, thereby regulating BMP signaling during cellular proliferation, differentiation, and programmed cell death. [provided by RefSeq, Jul 2008]","start":16461481,"end":16530580,"strand":-1,"description":"sclerostin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21748]"}, {"versioned_ensembl_gene_id":"ENSG00000232842.2","gene_symbol":"AL137845.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95973328,"end":95974315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282344.1","gene_symbol":"IGHV2-26","gene_name":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28455","summary":null,"start":106302166,"end":106302633,"strand":-1,"description":"immunoglobulin heavy variable 2-26 [Source:HGNC Symbol;Acc:HGNC:5575]"}, {"versioned_ensembl_gene_id":"ENSG00000203262.3","gene_symbol":"AL137845.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96070669,"end":96071778,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282239.1","gene_symbol":"IGHVIII-26-1","gene_name":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]","synonyms":"IGHV(III)-26-1","biotype":"IG_V_pseudogene","ncbi_id":"28347","summary":null,"start":106310188,"end":106310437,"strand":-1,"description":"immunoglobulin heavy variable (III)-26-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5698]"}, {"versioned_ensembl_gene_id":"ENSG00000205858.9","gene_symbol":"LRRC72","gene_name":"leucine rich repeat containing 72 [Source:HGNC Symbol;Acc:HGNC:42972]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506049","summary":null,"start":16526880,"end":16581568,"strand":1,"description":"leucine rich repeat containing 72 [Source:HGNC Symbol;Acc:HGNC:42972]"}, {"versioned_ensembl_gene_id":"ENSG00000282452.1","gene_symbol":"IGHVII-26-2","gene_name":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]","synonyms":"IGHV(II)-26-2","biotype":"IG_V_pseudogene","ncbi_id":"28373","summary":null,"start":106315422,"end":106315746,"strand":-1,"description":"immunoglobulin heavy variable (II)-26-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5674]"}, {"versioned_ensembl_gene_id":"ENSG00000109572.13","gene_symbol":"CLCN3","gene_name":"chloride voltage-gated channel 3 [Source:HGNC Symbol;Acc:HGNC:2021]","synonyms":"CLC3,ClC-3","biotype":"protein_coding","ncbi_id":"1182","summary":"This gene encodes a member of the voltage-gated chloride channel (ClC) family. The encoded protein is present in all cell types and localized in plasma membranes and in intracellular vesicles. It is a multi-pass membrane protein which contains a ClC domain and two additional C-terminal CBS (cystathionine beta-synthase) domains. The ClC domain catalyzes the selective flow of Cl- ions across cell membranes, and the CBS domain may have a regulatory function. This protein plays a role in both acidification and transmitter loading of GABAergic synaptic vesicles, and in smooth muscle cell activation and neointima formation. This protein is required for lysophosphatidic acid (LPA)-activated Cl- current activity and fibroblast-to-myofibroblast differentiation. The protein activity is regulated by Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) in glioma cells. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]","start":169612633,"end":169723673,"strand":1,"description":"chloride voltage-gated channel 3 [Source:HGNC Symbol;Acc:HGNC:2021]"}, {"versioned_ensembl_gene_id":"ENSG00000136275.10","gene_symbol":"C7orf69","gene_name":"chromosome 7 open reading frame 69 [Source:HGNC Symbol;Acc:HGNC:21911]","synonyms":"FLJ21075","biotype":"antisense_RNA","ncbi_id":"80099","summary":null,"start":47795291,"end":47819847,"strand":1,"description":"chromosome 7 open reading frame 69 [Source:HGNC Symbol;Acc:HGNC:21911]"}, {"versioned_ensembl_gene_id":"ENSG00000276806.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724507,"end":54736522,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000144118.13","gene_symbol":"RALB","gene_name":"RAS like proto-oncogene B [Source:HGNC Symbol;Acc:HGNC:9840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5899","summary":"This gene encodes a GTP-binding protein that belongs to the small GTPase superfamily and Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. [provided by RefSeq, Jul 2008]","start":120240064,"end":120294713,"strand":1,"description":"RAS like proto-oncogene B [Source:HGNC Symbol;Acc:HGNC:9840]"}, {"versioned_ensembl_gene_id":"ENSG00000251393.3","gene_symbol":"AC005280.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73462423,"end":73477175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146666.5","gene_symbol":"LINC00525","gene_name":"long intergenic non-protein coding RNA 525 [Source:HGNC Symbol;Acc:HGNC:40290]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"84847","summary":null,"start":47761476,"end":47766772,"strand":1,"description":"long intergenic non-protein coding RNA 525 [Source:HGNC Symbol;Acc:HGNC:40290]"}, {"versioned_ensembl_gene_id":"ENSG00000272537.1","gene_symbol":"AC005014.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16471184,"end":16471373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225507.1","gene_symbol":"AC069282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47956793,"end":47957318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158683.7","gene_symbol":"PKD1L1","gene_name":"polycystin 1 like 1, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:18053]","synonyms":"PRO19563","biotype":"protein_coding","ncbi_id":"168507","summary":"This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":47774652,"end":47948491,"strand":-1,"description":"polycystin 1 like 1, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:18053]"}, {"versioned_ensembl_gene_id":"ENSG00000164867.10","gene_symbol":"NOS3","gene_name":"nitric oxide synthase 3 [Source:HGNC Symbol;Acc:HGNC:7876]","synonyms":"eNOS,ECNOS","biotype":"protein_coding","ncbi_id":"4846","summary":"Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. Nitric oxide is synthesized from L-arginine by nitric oxide synthases. Variations in this gene are associated with susceptibility to coronary spasm. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":150990995,"end":151014588,"strand":1,"description":"nitric oxide synthase 3 [Source:HGNC Symbol;Acc:HGNC:7876]"}, {"versioned_ensembl_gene_id":"ENSG00000133961.19","gene_symbol":"NUMB","gene_name":"NUMB, endocytic adaptor protein [Source:HGNC Symbol;Acc:HGNC:8060]","synonyms":"C14orf41","biotype":"protein_coding","ncbi_id":"8650","summary":"The protein encoded by this gene plays a role in the determination of cell fates during development. The encoded protein, whose degradation is induced in a proteasome-dependent manner by MDM2, is a membrane-bound protein that has been shown to associate with EPS15, LNX1, and NOTCH1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":73275107,"end":73463642,"strand":-1,"description":"NUMB, endocytic adaptor protein [Source:HGNC Symbol;Acc:HGNC:8060]"}, {"versioned_ensembl_gene_id":"ENSG00000269806.1","gene_symbol":"BICRA-AS1","gene_name":"BICRA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51588]","synonyms":"GLTSCR1-AS1","biotype":"antisense_RNA","ncbi_id":"106144534","summary":null,"start":47615699,"end":47626395,"strand":-1,"description":"BICRA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51588]"}, {"versioned_ensembl_gene_id":"ENSG00000224899.1","gene_symbol":"AC019155.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125151326,"end":125153611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250768.1","gene_symbol":"DPP3P1","gene_name":"dipeptidyl peptidase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391657","summary":null,"start":64430909,"end":64433215,"strand":1,"description":"dipeptidyl peptidase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51349]"}, {"versioned_ensembl_gene_id":"ENSG00000244242.1","gene_symbol":"IFITM10","gene_name":"interferon induced transmembrane protein 10 [Source:HGNC Symbol;Acc:HGNC:40022]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402778","summary":null,"start":1732410,"end":1750591,"strand":-1,"description":"interferon induced transmembrane protein 10 [Source:HGNC Symbol;Acc:HGNC:40022]"}, {"versioned_ensembl_gene_id":"ENSG00000244063.1","gene_symbol":"AC104653.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113829390,"end":113831119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228857.2","gene_symbol":"AC104653.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113831049,"end":113843356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250802.6","gene_symbol":"ZBED3-AS1","gene_name":"ZBED3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44188]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"728723","summary":null,"start":77086740,"end":77166909,"strand":1,"description":"ZBED3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44188]"}, {"versioned_ensembl_gene_id":"ENSG00000280195.1","gene_symbol":"AC245140.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154396878,"end":154398816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267526.1","gene_symbol":"AC005702.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60063004,"end":60064782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215077.10","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"BRD2-IT1,FSRG1,NAT,D6S113E,KIAA9001,RING3","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":32897392,"end":32910230,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000141503.15","gene_symbol":"MINK1","gene_name":"misshapen like kinase 1 [Source:HGNC Symbol;Acc:HGNC:17565]","synonyms":"ZC3,YSK2,MINK,MAP4K6,B55","biotype":"protein_coding","ncbi_id":"50488","summary":"This gene encodes a serine/threonine kinase belonging to the germinal center kinase (GCK) family. The protein is structurally similar to the kinases that are related to NIK and may belong to a distinct subfamily of NIK-related kinases within the GCK family. Studies of the mouse homolog indicate an up-regulation of expression in the course of postnatal mouse cerebral development and activation of the cJun N-terminal kinase (JNK) and the p38 pathways. [provided by RefSeq, Mar 2016]","start":4833388,"end":4898061,"strand":1,"description":"misshapen like kinase 1 [Source:HGNC Symbol;Acc:HGNC:17565]"}, {"versioned_ensembl_gene_id":"ENSG00000253141.1","gene_symbol":"AC008632.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173463500,"end":173484584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230739.1","gene_symbol":"AL392003.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":162824795,"end":162849467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180573.9","gene_symbol":"HIST1H2AC","gene_name":"histone cluster 1 H2A family member c [Source:HGNC Symbol;Acc:HGNC:4733]","synonyms":"H2AFL","biotype":"protein_coding","ncbi_id":"8334","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26124145,"end":26139116,"strand":1,"description":"histone cluster 1 H2A family member c [Source:HGNC Symbol;Acc:HGNC:4733]"}, {"versioned_ensembl_gene_id":"ENSG00000205865.4","gene_symbol":"FAM99B","gene_name":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]","synonyms":"DKFZp781M09150","biotype":"antisense_RNA","ncbi_id":"100132464","summary":null,"start":1683269,"end":1685629,"strand":-1,"description":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]"}, {"versioned_ensembl_gene_id":"ENSG00000205866.3","gene_symbol":"FAM99A","gene_name":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]","synonyms":"FLJ42833","biotype":"lincRNA","ncbi_id":"387742","summary":null,"start":1665597,"end":1667856,"strand":1,"description":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]"}, {"versioned_ensembl_gene_id":"ENSG00000162877.12","gene_symbol":"PM20D1","gene_name":"peptidase M20 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26518]","synonyms":"FLJ32569,Cps1","biotype":"protein_coding","ncbi_id":"148811","summary":null,"start":205828022,"end":205850132,"strand":-1,"description":"peptidase M20 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26518]"}, {"versioned_ensembl_gene_id":"ENSG00000167755.14","gene_symbol":"KLK6","gene_name":"kallikrein related peptidase 6 [Source:HGNC Symbol;Acc:HGNC:6367]","synonyms":"PRSS9,PRSS18,neurosin,Klk7,Bssp","biotype":"protein_coding","ncbi_id":"5653","summary":"This gene encodes a member of the kallikrein subfamily of the peptidase S1 family of serine proteases. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. The encoded preproprotein is proteolytically processed to generate the mature protease. Expression of this protease is regulated by steroid hormones and may be elevated in multiple human cancers and in serum from psoriasis patients. The encoded protease may participate in the cleavage of amyloid precursor protein and alpha-synuclein, thus implicating this protease in Alzheimer's and Parkinson's disease, respectively. This gene is located in a gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":50958631,"end":50969673,"strand":-1,"description":"kallikrein related peptidase 6 [Source:HGNC Symbol;Acc:HGNC:6367]"}, {"versioned_ensembl_gene_id":"ENSG00000177469.12","gene_symbol":"CAVIN1","gene_name":"caveolae associated protein 1 [Source:HGNC Symbol;Acc:HGNC:9688]","synonyms":"CGL4,cavin-1,PTRF","biotype":"protein_coding","ncbi_id":"284119","summary":"This gene encodes a protein that enables the dissociation of paused ternary polymerase I transcription complexes from the 3' end of pre-rRNA transcripts. This protein regulates rRNA transcription by promoting the dissociation of transcription complexes and the reinitiation of polymerase I on nascent rRNA transcripts. This protein also localizes to caveolae at the plasma membrane and is thought to play a critical role in the formation of caveolae and the stabilization of caveolins. This protein translocates from caveolae to the cytoplasm after insulin stimulation. Caveolae contain truncated forms of this protein and may be the site of phosphorylation-dependent proteolysis. This protein is also thought to modify lipid metabolism and insulin-regulated gene expression. Mutations in this gene result in a disorder characterized by generalized lipodystrophy and muscular dystrophy. [provided by RefSeq, Nov 2009]","start":42402452,"end":42423517,"strand":-1,"description":"caveolae associated protein 1 [Source:HGNC Symbol;Acc:HGNC:9688]"}, {"versioned_ensembl_gene_id":"ENSG00000167272.10","gene_symbol":"POP5","gene_name":"POP5 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:17689]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51367","summary":null,"start":120578764,"end":120581398,"strand":-1,"description":"POP5 homolog, ribonuclease P/MRP subunit [Source:HGNC Symbol;Acc:HGNC:17689]"}, {"versioned_ensembl_gene_id":"ENSG00000270747.1","gene_symbol":"AL606490.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48336899,"end":48337169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237512.6","gene_symbol":"UNC5B-AS1","gene_name":"UNC5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45096]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"728978","summary":null,"start":71217224,"end":71218228,"strand":-1,"description":"UNC5B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45096]"}, {"versioned_ensembl_gene_id":"ENSG00000180871.7","gene_symbol":"CXCR2","gene_name":"C-X-C motif chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:6027]","synonyms":"IL8RB,CMKAR2,CD182","biotype":"protein_coding","ncbi_id":"3579","summary":"The protein encoded by this gene is a member of the G-protein-coupled receptor family. This protein is a receptor for interleukin 8 (IL8). It binds to IL8 with high affinity, and transduces the signal through a G-protein activated second messenger system. This receptor also binds to chemokine (C-X-C motif) ligand 1 (CXCL1/MGSA), a protein with melanoma growth stimulating activity, and has been shown to be a major component required for serum-dependent melanoma cell growth. This receptor mediates neutrophil migration to sites of inflammation. The angiogenic effects of IL8 in intestinal microvascular endothelial cells are found to be mediated by this receptor. Knockout studies in mice suggested that this receptor controls the positioning of oligodendrocyte precursors in developing spinal cord by arresting their migration. This gene, IL8RA, a gene encoding another high affinity IL8 receptor, as well as IL8RBP, a pseudogene of IL8RB, form a gene cluster in a region mapped to chromosome 2q33-q36. Alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2009]","start":218125289,"end":218137253,"strand":1,"description":"C-X-C motif chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:6027]"}, {"versioned_ensembl_gene_id":"ENSG00000197403.4","gene_symbol":"OR6N1","gene_name":"olfactory receptor family 6 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:15034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128372","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158747814,"end":158772195,"strand":-1,"description":"olfactory receptor family 6 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:15034]"}, {"versioned_ensembl_gene_id":"ENSG00000164168.7","gene_symbol":"TMEM184C","gene_name":"transmembrane protein 184C [Source:HGNC Symbol;Acc:HGNC:25587]","synonyms":"TMEM34,FLJ10846","biotype":"protein_coding","ncbi_id":"55751","summary":null,"start":147617383,"end":147672044,"strand":1,"description":"transmembrane protein 184C [Source:HGNC Symbol;Acc:HGNC:25587]"}, {"versioned_ensembl_gene_id":"ENSG00000260339.1","gene_symbol":"HEXA-AS1","gene_name":"HEXA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25810]","synonyms":"FLJ13315,C15orf34","biotype":"antisense_RNA","ncbi_id":"80072","summary":null,"start":72376113,"end":72378788,"strand":1,"description":"HEXA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25810]"}, {"versioned_ensembl_gene_id":"ENSG00000283526.1","gene_symbol":"AL160276.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":131545514,"end":131558620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233555.2","gene_symbol":"AL591438.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63581254,"end":63581834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226669.2","gene_symbol":"AL354977.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3684076,"end":3689626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137675.4","gene_symbol":"MMP27","gene_name":"matrix metallopeptidase 27 [Source:HGNC Symbol;Acc:HGNC:14250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64066","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. [provided by RefSeq, Jul 2008]","start":102691487,"end":102705806,"strand":-1,"description":"matrix metallopeptidase 27 [Source:HGNC Symbol;Acc:HGNC:14250]"}, {"versioned_ensembl_gene_id":"ENSG00000137674.3","gene_symbol":"MMP20","gene_name":"matrix metallopeptidase 20 [Source:HGNC Symbol;Acc:HGNC:7167]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9313","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The protein encoded by this gene degrades amelogenin, the major protein component of dental enamel matrix, and thus thought to play a role in tooth enamel formation. A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta. This gene is part of a cluster of MMP genes located on chromosome 11q22.3. [provided by RefSeq, Aug 2011]","start":102576835,"end":102625332,"strand":-1,"description":"matrix metallopeptidase 20 [Source:HGNC Symbol;Acc:HGNC:7167]"}, {"versioned_ensembl_gene_id":"ENSG00000256916.1","gene_symbol":"AP000851.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102606916,"end":102628070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273327.1","gene_symbol":"OR6L2P","gene_name":"olfactory receptor family 6 subfamily L member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15125]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81356","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":133430394,"end":133431318,"strand":-1,"description":"olfactory receptor family 6 subfamily L member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15125]"}, {"versioned_ensembl_gene_id":"ENSG00000259020.3","gene_symbol":"AL049872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92026566,"end":92026887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160226.15","gene_symbol":"C21orf2","gene_name":"chromosome 21 open reading frame 2 [Source:HGNC Symbol;Acc:HGNC:1260]","synonyms":"YF5,LRRC76,A2","biotype":"protein_coding","ncbi_id":"755","summary":"Four alternatively spliced transcript variants encoding four different isoforms have been found for this nuclear gene. All isoforms contain leucine-rich repeats. Three of these isoforms are mitochondrial proteins and one of them lacks the target peptide, so is not located in mitochondrion. This gene is down-regulated in Down syndrome (DS) brain, which may represent mitochondrial dysfunction in DS patients. [provided by RefSeq, Sep 2012]","start":44328944,"end":44339402,"strand":-1,"description":"chromosome 21 open reading frame 2 [Source:HGNC Symbol;Acc:HGNC:1260]"}, {"versioned_ensembl_gene_id":"ENSG00000279089.1","gene_symbol":"AC005839.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51183191,"end":51186403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184441.4","gene_symbol":"AP001062.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44331234,"end":44335851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104856.13","gene_symbol":"RELB","gene_name":"RELB proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9956]","synonyms":"REL-B","biotype":"protein_coding","ncbi_id":"5971","summary":null,"start":45001430,"end":45038198,"strand":1,"description":"RELB proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9956]"}, {"versioned_ensembl_gene_id":"ENSG00000167065.13","gene_symbol":"DUSP18","gene_name":"dual specificity phosphatase 18 [Source:HGNC Symbol;Acc:HGNC:18484]","synonyms":"DUSP20","biotype":"protein_coding","ncbi_id":"150290","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP18 contains the consensus DUSP C-terminal catalytic domain but lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":30652051,"end":30667890,"strand":-1,"description":"dual specificity phosphatase 18 [Source:HGNC Symbol;Acc:HGNC:18484]"}, {"versioned_ensembl_gene_id":"ENSG00000237027.1","gene_symbol":"AL159174.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89560875,"end":89567044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258903.1","gene_symbol":"AL390816.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62103378,"end":62117175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278463.1","gene_symbol":"HIST1H2AB","gene_name":"histone cluster 1 H2A family member b [Source:HGNC Symbol;Acc:HGNC:4734]","synonyms":"H2AFM,H2A/m","biotype":"protein_coding","ncbi_id":"8335","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26033176,"end":26033568,"strand":-1,"description":"histone cluster 1 H2A family member b [Source:HGNC Symbol;Acc:HGNC:4734]"}, {"versioned_ensembl_gene_id":"ENSG00000267892.1","gene_symbol":"AC022144.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38738284,"end":38739863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261652.2","gene_symbol":"C15orf65","gene_name":"chromosome 15 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:44654]","synonyms":"FLJ27352","biotype":"protein_coding","ncbi_id":"145788","summary":null,"start":55408548,"end":55418764,"strand":1,"description":"chromosome 15 open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:44654]"}, {"versioned_ensembl_gene_id":"ENSG00000223393.1","gene_symbol":"AL118511.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230874846,"end":230879015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133710.15","gene_symbol":"SPINK5","gene_name":"serine peptidase inhibitor, Kazal type 5 [Source:HGNC Symbol;Acc:HGNC:15464]","synonyms":"LEKTI,FLJ99794,FLJ97596,FLJ97536,VAKTI,FLJ21544,NS,DKFZp686K19184,NETS,LETKI","biotype":"protein_coding","ncbi_id":"11005","summary":"This gene encodes a multidomain serine protease inhibitor that contains 15 potential inhibitory domains. The encoded preproprotein is proteolytically processed to generate multiple protein products, which may exhibit unique activities and specificities. These proteins may play a role in skin and hair morphogenesis, as well as anti-inflammatory and antimicrobial protection of mucous epithelia. Mutations in this gene may result in Netherton syndrome, a disorder characterized by ichthyosis, defective cornification, and atopy. This gene is present in a gene cluster on chromosome 5. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":148025683,"end":148137289,"strand":1,"description":"serine peptidase inhibitor, Kazal type 5 [Source:HGNC Symbol;Acc:HGNC:15464]"}, {"versioned_ensembl_gene_id":"ENSG00000251055.2","gene_symbol":"AC097491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63128311,"end":63143881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230673.3","gene_symbol":"PABPC1P3","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:8560]","synonyms":"PABPCP3,PABP3","biotype":"processed_pseudogene","ncbi_id":"26978","summary":null,"start":74583088,"end":74583546,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:8560]"}, {"versioned_ensembl_gene_id":"ENSG00000280463.1","gene_symbol":"AC171558.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21716735,"end":21717356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271155.1","gene_symbol":"AL161729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95506235,"end":95507636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248908.1","gene_symbol":"LINC02239","gene_name":"long intergenic non-protein coding RNA 2239 [Source:HGNC Symbol;Acc:HGNC:27969]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340107","summary":null,"start":24835280,"end":24840583,"strand":-1,"description":"long intergenic non-protein coding RNA 2239 [Source:HGNC Symbol;Acc:HGNC:27969]"}, {"versioned_ensembl_gene_id":"ENSG00000119965.12","gene_symbol":"C10orf88","gene_name":"chromosome 10 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25822]","synonyms":"FLJ13490,Em:AC073585.5","biotype":"protein_coding","ncbi_id":"80007","summary":null,"start":122930903,"end":122954403,"strand":-1,"description":"chromosome 10 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:25822]"}, {"versioned_ensembl_gene_id":"ENSG00000160654.9","gene_symbol":"CD3G","gene_name":"CD3g molecule [Source:HGNC Symbol;Acc:HGNC:1675]","synonyms":null,"biotype":"protein_coding","ncbi_id":"917","summary":"The protein encoded by this gene is the CD3-gamma polypeptide, which together with CD3-epsilon, -delta and -zeta, and the T-cell receptor alpha/beta and gamma/delta heterodimers, forms the T-cell receptor-CD3 complex. This complex plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. The genes encoding the epsilon, gamma and delta polypeptides are located in the same cluster on chromosome 11. Defects in this gene are associated with T cell immunodeficiency. [provided by RefSeq, Jul 2008]","start":118344344,"end":118355161,"strand":1,"description":"CD3g molecule [Source:HGNC Symbol;Acc:HGNC:1675]"}, {"versioned_ensembl_gene_id":"ENSG00000231237.1","gene_symbol":"OR6K1P","gene_name":"olfactory receptor family 6 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15028]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81449","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158694539,"end":158695509,"strand":-1,"description":"olfactory receptor family 6 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15028]"}, {"versioned_ensembl_gene_id":"ENSG00000250988.7","gene_symbol":"SNHG21","gene_name":"small nucleolar RNA host gene 21 [Source:HGNC Symbol;Acc:HGNC:50284]","synonyms":"SCARNA15HG,RP11-752G15.6,FSD2-AS1","biotype":"antisense_RNA","ncbi_id":"100505616","summary":null,"start":82750564,"end":82757206,"strand":1,"description":"small nucleolar RNA host gene 21 [Source:HGNC Symbol;Acc:HGNC:50284]"}, {"versioned_ensembl_gene_id":"ENSG00000189343.7","gene_symbol":"AC004448.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19445970,"end":19446852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279702.1","gene_symbol":"AL356266.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":102299790,"end":102300272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176115.9","gene_symbol":"AQP7P4","gene_name":"aquaporin 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32056]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132938","summary":null,"start":63127359,"end":63143401,"strand":1,"description":"aquaporin 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32056]"}, {"versioned_ensembl_gene_id":"ENSG00000175066.15","gene_symbol":"GK5","gene_name":"glycerol kinase 5 (putative) [Source:HGNC Symbol;Acc:HGNC:28635]","synonyms":"MGC40579","biotype":"protein_coding","ncbi_id":"256356","summary":null,"start":142157527,"end":142225607,"strand":-1,"description":"glycerol kinase 5 (putative) [Source:HGNC Symbol;Acc:HGNC:28635]"}, {"versioned_ensembl_gene_id":"ENSG00000279175.1","gene_symbol":"AL033543.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44102779,"end":44116232,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248466.1","gene_symbol":"AC098827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36065060,"end":36065726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171606.17","gene_symbol":"ZNF274","gene_name":"zinc finger protein 274 [Source:HGNC Symbol;Acc:HGNC:13068]","synonyms":"ZSCAN51,ZKSCAN19","biotype":"protein_coding","ncbi_id":"10782","summary":"This gene encodes a zinc finger protein containing five C2H2-type zinc finger domains, one or two Kruppel-associated box A (KRAB A) domains, and a leucine-rich domain. The encoded protein has been suggested to be a transcriptional repressor. It localizes predominantly to the nucleolus. Alternatively spliced transcript variants encoding different isoforms exist. These variants utilize alternative polyadenylation signals. [provided by RefSeq, Jul 2008]","start":58183029,"end":58213562,"strand":1,"description":"zinc finger protein 274 [Source:HGNC Symbol;Acc:HGNC:13068]"}, {"versioned_ensembl_gene_id":"ENSG00000235512.1","gene_symbol":"TAB3-AS2","gene_name":"TAB3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40013]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873926","summary":null,"start":30854321,"end":30854707,"strand":1,"description":"TAB3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40013]"}, {"versioned_ensembl_gene_id":"ENSG00000114850.6","gene_symbol":"SSR3","gene_name":"signal sequence receptor subunit 3 [Source:HGNC Symbol;Acc:HGNC:11325]","synonyms":"TRAPG","biotype":"protein_coding","ncbi_id":"6747","summary":"The signal sequence receptor (SSR) is a glycosylated endoplasmic reticulum (ER) membrane receptor associated with protein translocation across the ER membrane. The SSR is comprised of four membrane proteins/subunits: alpha, beta, gamma, and delta. The first two are glycosylated subunits and the latter two are non-glycosylated subunits. This gene encodes the gamma subunit, which is predicted to span the membrane four times. [provided by RefSeq, Aug 2010]","start":156540140,"end":156555184,"strand":-1,"description":"signal sequence receptor subunit 3 [Source:HGNC Symbol;Acc:HGNC:11325]"}, {"versioned_ensembl_gene_id":"ENSG00000133687.15","gene_symbol":"TMTC1","gene_name":"transmembrane and tetratricopeptide repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:24099]","synonyms":"FLJ31400,ARG99,OLF,FLJ41625","biotype":"protein_coding","ncbi_id":"83857","summary":null,"start":29500840,"end":29784759,"strand":-1,"description":"transmembrane and tetratricopeptide repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:24099]"}, {"versioned_ensembl_gene_id":"ENSG00000257757.1","gene_symbol":"OR6C7P","gene_name":"olfactory receptor family 6 subfamily C member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:31306]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390322","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55342841,"end":55343774,"strand":1,"description":"olfactory receptor family 6 subfamily C member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:31306]"}, {"versioned_ensembl_gene_id":"ENSG00000153292.15","gene_symbol":"ADGRF1","gene_name":"adhesion G protein-coupled receptor F1 [Source:HGNC Symbol;Acc:HGNC:18990]","synonyms":"PGR19,hGPCR36,GPR110","biotype":"protein_coding","ncbi_id":"266977","summary":null,"start":46997703,"end":47042363,"strand":-1,"description":"adhesion G protein-coupled receptor F1 [Source:HGNC Symbol;Acc:HGNC:18990]"}, {"versioned_ensembl_gene_id":"ENSG00000253117.4","gene_symbol":"OC90","gene_name":"otoconin 90 [Source:HGNC Symbol;Acc:HGNC:8100]","synonyms":"PLA2L","biotype":"protein_coding","ncbi_id":"729330","summary":null,"start":132024220,"end":132059380,"strand":-1,"description":"otoconin 90 [Source:HGNC Symbol;Acc:HGNC:8100]"}, {"versioned_ensembl_gene_id":"ENSG00000275584.5","gene_symbol":"LILRA6","gene_name":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]","synonyms":"CD85b,LILRB6,ILT8","biotype":"protein_coding","ncbi_id":"79168","summary":null,"start":54238892,"end":54243172,"strand":-1,"description":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]"}, {"versioned_ensembl_gene_id":"ENSG00000068724.15","gene_symbol":"TTC7A","gene_name":"tetratricopeptide repeat domain 7A [Source:HGNC Symbol;Acc:HGNC:19750]","synonyms":"TTC7,KIAA1140","biotype":"protein_coding","ncbi_id":"57217","summary":"This gene encodes a protein containing tetratricopeptide repeats. Mutations in this gene disrupt intestinal development and can cause early onset inflammatory bowel disease and intestinal atresia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":46916157,"end":47076137,"strand":1,"description":"tetratricopeptide repeat domain 7A [Source:HGNC Symbol;Acc:HGNC:19750]"}, {"versioned_ensembl_gene_id":"ENSG00000225187.1","gene_symbol":"AC073283.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47067822,"end":47071204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198515.13","gene_symbol":"CNGA1","gene_name":"cyclic nucleotide gated channel alpha 1 [Source:HGNC Symbol;Acc:HGNC:2148]","synonyms":"RP49,RCNCa,RCNC1,CNG1,CNCG1,CNCG","biotype":"protein_coding","ncbi_id":"1259","summary":"The protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Multiple transcript variants have been found for this gene. [provided by RefSeq, Oct 2019]","start":47935977,"end":48016672,"strand":-1,"description":"cyclic nucleotide gated channel alpha 1 [Source:HGNC Symbol;Acc:HGNC:2148]"}, {"versioned_ensembl_gene_id":"ENSG00000282917.1","gene_symbol":"AC107068.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47831385,"end":47896709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265313.5","gene_symbol":"LINC01476","gene_name":"long intergenic non-protein coding RNA 1476 [Source:HGNC Symbol;Acc:HGNC:51117]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927728","summary":null,"start":59430869,"end":59526946,"strand":-1,"description":"long intergenic non-protein coding RNA 1476 [Source:HGNC Symbol;Acc:HGNC:51117]"}, {"versioned_ensembl_gene_id":"ENSG00000214855.9","gene_symbol":"APOC1P1","gene_name":"apolipoprotein C1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:608]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"342","summary":null,"start":44926804,"end":44931386,"strand":1,"description":"apolipoprotein C1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:608]"}, {"versioned_ensembl_gene_id":"ENSG00000176208.8","gene_symbol":"ATAD5","gene_name":"ATPase family, AAA domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25752]","synonyms":"FRAG1,FLJ12735,ELG1,C17orf41","biotype":"protein_coding","ncbi_id":"79915","summary":null,"start":30831970,"end":30895869,"strand":1,"description":"ATPase family, AAA domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25752]"}, {"versioned_ensembl_gene_id":"ENSG00000275990.3","gene_symbol":"NCF4","gene_name":"neutrophil cytosolic factor 4 [Source:HGNC Symbol;Acc:HGNC:7662]","synonyms":"p40phox,SH3PXD4","biotype":"protein_coding","ncbi_id":"4689","summary":"The protein encoded by this gene is a cytosolic regulatory component of the superoxide-producing phagocyte NADPH-oxidase, a multicomponent enzyme system important for host defense. This protein is preferentially expressed in cells of myeloid lineage. It interacts primarily with neutrophil cytosolic factor 2 (NCF2/p67-phox) to form a complex with neutrophil cytosolic factor 1 (NCF1/p47-phox), which further interacts with the small G protein RAC1 and translocates to the membrane upon cell stimulation. This complex then activates flavocytochrome b, the membrane-integrated catalytic core of the enzyme system. The PX domain of this protein can bind phospholipid products of the PI(3) kinase, which suggests its role in PI(3) kinase-mediated signaling events. The phosphorylation of this protein was found to negatively regulate the enzyme activity. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":36860995,"end":36880544,"strand":1,"description":"neutrophil cytosolic factor 4 [Source:HGNC Symbol;Acc:HGNC:7662]"}, {"versioned_ensembl_gene_id":"ENSG00000227582.2","gene_symbol":"ADGRF5P1","gene_name":"adhesion G protein-coupled receptor F5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32922]","synonyms":"GPR116P1","biotype":"transcribed_processed_pseudogene","ncbi_id":"389740","summary":null,"start":62860873,"end":62864957,"strand":-1,"description":"adhesion G protein-coupled receptor F5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32922]"}, {"versioned_ensembl_gene_id":"ENSG00000129744.2","gene_symbol":"ART1","gene_name":"ADP-ribosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:723]","synonyms":"CD296,ART2","biotype":"protein_coding","ncbi_id":"417","summary":"ADP-ribosyltransferase catalyzes the ADP-ribosylation of arginine residues in proteins. Mono-ADP-ribosylation is a posttranslational modification of proteins that is interfered with by a variety of bacterial toxins including cholera, pertussis, and heat-labile enterotoxins of E. coli. The amino acid sequence consists of predominantly hydrophobic N- and C-terminal regions, which is characteristic of glycosylphosphatidylinositol (GPI)-anchored proteins. This gene was previously designated ART2. [provided by RefSeq, Jul 2008]","start":3645128,"end":3664416,"strand":1,"description":"ADP-ribosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:723]"}, {"versioned_ensembl_gene_id":"ENSG00000229857.1","gene_symbol":"AL353637.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76992099,"end":76993108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255624.2","gene_symbol":"AC073585.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":122879851,"end":122898024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272269.1","gene_symbol":"AL138724.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17706257,"end":17707344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232316.1","gene_symbol":"LINC02518","gene_name":"long intergenic non-protein coding RNA 2518 [Source:HGNC Symbol;Acc:HGNC:53509]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377957","summary":null,"start":113428540,"end":113433421,"strand":-1,"description":"long intergenic non-protein coding RNA 2518 [Source:HGNC Symbol;Acc:HGNC:53509]"}, {"versioned_ensembl_gene_id":"ENSG00000122859.4","gene_symbol":"NEUROG3","gene_name":"neurogenin 3 [Source:HGNC Symbol;Acc:HGNC:13806]","synonyms":"ngn3,Math4B,bHLHa7,Atoh5","biotype":"protein_coding","ncbi_id":"50674","summary":"The protein encoded by this gene is a basic helix-loop-helix (bHLH) transcription factor involved in neurogenesis. The encoded protein likely acts as a heterodimer with another bHLH protein. Defects in this gene are a cause of congenital malabsorptive diarrhea 4 (DIAR4).[provided by RefSeq, May 2010]","start":69571698,"end":69573238,"strand":-1,"description":"neurogenin 3 [Source:HGNC Symbol;Acc:HGNC:13806]"}, {"versioned_ensembl_gene_id":"ENSG00000263655.1","gene_symbol":"AC090125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73914405,"end":74034161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271600.1","gene_symbol":"AP000942.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102308557,"end":102308797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255046.1","gene_symbol":"AC069185.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11797928,"end":11802568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282906.1","gene_symbol":"AL513321.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65123667,"end":65141185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263711.5","gene_symbol":"AC079062.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73151241,"end":73264480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149573.8","gene_symbol":"MPZL2","gene_name":"myelin protein zero like 2 [Source:HGNC Symbol;Acc:HGNC:3496]","synonyms":"EVA1,EVA","biotype":"protein_coding","ncbi_id":"10205","summary":"Thymus development depends on a complex series of interactions between thymocytes and the stromal component of the organ. Epithelial V-like antigen (EVA) is expressed in thymus epithelium and strongly downregulated by thymocyte developmental progression. This gene is expressed in the thymus and in several epithelial structures early in embryogenesis. It is highly homologous to the myelin protein zero and, in thymus-derived epithelial cell lines, is poorly soluble in nonionic detergents, strongly suggesting an association to the cytoskeleton. Its capacity to mediate cell adhesion through a homophilic interaction and its selective regulation by T cell maturation might imply the participation of EVA in the earliest phases of thymus organogenesis. The protein bears a characteristic V-type domain and two potential N-glycosylation sites in the extracellular domain; a putative serine phosphorylation site for casein kinase 2 is also present in the cytoplasmic tail. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":118253403,"end":118264536,"strand":-1,"description":"myelin protein zero like 2 [Source:HGNC Symbol;Acc:HGNC:3496]"}, {"versioned_ensembl_gene_id":"ENSG00000223722.3","gene_symbol":"AC023157.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31754720,"end":31755121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231573.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33389703,"end":33395155,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000267370.1","gene_symbol":"AC008752.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9756152,"end":9756863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272221.1","gene_symbol":"AL645933.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31394289,"end":31395495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270024.5","gene_symbol":"C8orf44-SGK3","gene_name":"C8orf44-SGK3 readthrough [Source:HGNC Symbol;Acc:HGNC:48354]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533105","summary":"This locus represents naturally occurring read-through transcription between the neighboring putative uncharacterized protein C8orf44 (GeneID 56260) and serine/threonine-protein kinase Sgk3 (GeneID 23678) genes on chromosome 8. The read-through transcript produces a protein that shares sequence identity with the downstream gene product. [provided by RefSeq, Feb 2011]","start":66667596,"end":66860472,"strand":1,"description":"C8orf44-SGK3 readthrough [Source:HGNC Symbol;Acc:HGNC:48354]"}, {"versioned_ensembl_gene_id":"ENSG00000221838.9","gene_symbol":"AP4M1","gene_name":"adaptor related protein complex 4 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:574]","synonyms":"SPG50,MU-ARP2,MU-4","biotype":"protein_coding","ncbi_id":"9179","summary":"This gene encodes a subunit of the heterotetrameric AP-4 complex. The encoded protein belongs to the adaptor complexes medium subunits family. This AP-4 complex is involved in the recognition and sorting of cargo proteins with tyrosine-based motifs from the trans-golgi network to the endosomal-lysosomal system. [provided by RefSeq, Jul 2008]","start":100101549,"end":100110345,"strand":1,"description":"adaptor related protein complex 4 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:574]"}, {"versioned_ensembl_gene_id":"ENSG00000132855.4","gene_symbol":"ANGPTL3","gene_name":"angiopoietin like 3 [Source:HGNC Symbol;Acc:HGNC:491]","synonyms":"ANGPT5","biotype":"protein_coding","ncbi_id":"27329","summary":"This gene encodes a member of a family of secreted proteins that function in angiogenesis. The encoded protein, which is expressed predominantly in the liver, is further processed into an N-terminal coiled-coil domain-containing chain and a C-terminal fibrinogen chain. The N-terminal chain is important for lipid metabolism, while the C-terminal chain may be involved in angiogenesis. Mutations in this gene cause familial hypobetalipoproteinemia type 2. [provided by RefSeq, Aug 2015]","start":62597487,"end":62606159,"strand":1,"description":"angiopoietin like 3 [Source:HGNC Symbol;Acc:HGNC:491]"}, {"versioned_ensembl_gene_id":"ENSG00000257083.5","gene_symbol":"AC073530.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67035508,"end":67096406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256248.1","gene_symbol":"AC134511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66891876,"end":67069162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266537.1","gene_symbol":"SPDYE22P","gene_name":"speedy/RINGO cell cycle regulator family member E22, pseudogene [Source:HGNC Symbol;Acc:HGNC:51518]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420854","summary":null,"start":59174983,"end":59181787,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E22, pseudogene [Source:HGNC Symbol;Acc:HGNC:51518]"}, {"versioned_ensembl_gene_id":"ENSG00000214357.8","gene_symbol":"NEURL1B","gene_name":"neuralized E3 ubiquitin protein ligase 1B [Source:HGNC Symbol;Acc:HGNC:35422]","synonyms":"Neur2,DKFZP761M1511","biotype":"protein_coding","ncbi_id":"54492","summary":null,"start":172641266,"end":172691540,"strand":1,"description":"neuralized E3 ubiquitin protein ligase 1B [Source:HGNC Symbol;Acc:HGNC:35422]"}, {"versioned_ensembl_gene_id":"ENSG00000225334.1","gene_symbol":"AL391811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":224766900,"end":224773341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151715.7","gene_symbol":"TMEM45B","gene_name":"transmembrane protein 45B [Source:HGNC Symbol;Acc:HGNC:25194]","synonyms":"FLJ40787,BC016153","biotype":"protein_coding","ncbi_id":"120224","summary":null,"start":129815819,"end":129860003,"strand":1,"description":"transmembrane protein 45B [Source:HGNC Symbol;Acc:HGNC:25194]"}, {"versioned_ensembl_gene_id":"ENSG00000152467.9","gene_symbol":"ZSCAN1","gene_name":"zinc finger and SCAN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23712]","synonyms":"ZNF915,FLJ33779","biotype":"protein_coding","ncbi_id":"284312","summary":null,"start":58034032,"end":58054631,"strand":1,"description":"zinc finger and SCAN domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23712]"}, {"versioned_ensembl_gene_id":"ENSG00000135211.5","gene_symbol":"TMEM60","gene_name":"transmembrane protein 60 [Source:HGNC Symbol;Acc:HGNC:21754]","synonyms":"DC32,C7orf35","biotype":"protein_coding","ncbi_id":"85025","summary":null,"start":77793728,"end":77798580,"strand":-1,"description":"transmembrane protein 60 [Source:HGNC Symbol;Acc:HGNC:21754]"}, {"versioned_ensembl_gene_id":"ENSG00000225397.1","gene_symbol":"AC244505.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52722338,"end":52722524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229791.1","gene_symbol":"AL356259.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19408042,"end":19409529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267490.1","gene_symbol":"AC008759.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9724008,"end":9725086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249870.1","gene_symbol":"AC005920.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51042524,"end":51085471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282806.1","gene_symbol":"AC068400.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37388354,"end":37389394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143390.17","gene_symbol":"RFX5","gene_name":"regulatory factor X5 [Source:HGNC Symbol;Acc:HGNC:9986]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5993","summary":"A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined. [provided by RefSeq, Jul 2008]","start":151340640,"end":151347357,"strand":-1,"description":"regulatory factor X5 [Source:HGNC Symbol;Acc:HGNC:9986]"}, {"versioned_ensembl_gene_id":"ENSG00000183439.7","gene_symbol":"TRIM61","gene_name":"tripartite motif containing 61 [Source:HGNC Symbol;Acc:HGNC:24339]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"391712","summary":null,"start":164954446,"end":164977668,"strand":-1,"description":"tripartite motif containing 61 [Source:HGNC Symbol;Acc:HGNC:24339]"}, {"versioned_ensembl_gene_id":"ENSG00000006607.13","gene_symbol":"FARP2","gene_name":"FERM, ARH/RhoGEF and pleckstrin domain protein 2 [Source:HGNC Symbol;Acc:HGNC:16460]","synonyms":"PLEKHC3,KIAA0793,FRG,FIR","biotype":"protein_coding","ncbi_id":"9855","summary":null,"start":241356243,"end":241494841,"strand":1,"description":"FERM, ARH/RhoGEF and pleckstrin domain protein 2 [Source:HGNC Symbol;Acc:HGNC:16460]"}, {"versioned_ensembl_gene_id":"ENSG00000224232.1","gene_symbol":"AC005104.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":241478316,"end":241478993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280780.2","gene_symbol":"JAKMIP2-AS1","gene_name":"JAKMIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27203]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"153469","summary":null,"start":147559994,"end":147662009,"strand":1,"description":"JAKMIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27203]"}, {"versioned_ensembl_gene_id":"ENSG00000231949.1","gene_symbol":"AL161638.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30415825,"end":30421108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260484.1","gene_symbol":"AC131902.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53388701,"end":53390872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256879.1","gene_symbol":"AC129102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20361732,"end":20370262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164104.11","gene_symbol":"HMGB2","gene_name":"high mobility group box 2 [Source:HGNC Symbol;Acc:HGNC:5000]","synonyms":"HMG2","biotype":"protein_coding","ncbi_id":"3148","summary":"This gene encodes a member of the non-histone chromosomal high mobility group protein family. The proteins of this family are chromatin-associated and ubiquitously distributed in the nucleus of higher eukaryotic cells. In vitro studies have demonstrated that this protein is able to efficiently bend DNA and form DNA circles. These studies suggest a role in facilitating cooperative interactions between cis-acting proteins by promoting DNA flexibility. This protein was also reported to be involved in the final ligation step in DNA end-joining processes of DNA double-strand breaks repair and V(D)J recombination. [provided by RefSeq, Jul 2008]","start":173331695,"end":173335125,"strand":-1,"description":"high mobility group box 2 [Source:HGNC Symbol;Acc:HGNC:5000]"}, {"versioned_ensembl_gene_id":"ENSG00000173285.4","gene_symbol":"OR10K1","gene_name":"olfactory receptor family 10 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391109","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158461574,"end":158470857,"strand":1,"description":"olfactory receptor family 10 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14693]"}, {"versioned_ensembl_gene_id":"ENSG00000122335.13","gene_symbol":"SERAC1","gene_name":"serine active site containing 1 [Source:HGNC Symbol;Acc:HGNC:21061]","synonyms":"FLJ14917","biotype":"protein_coding","ncbi_id":"84947","summary":"The protein encoded by this gene is a phosphatidylglycerol remodeling protein found at the interface of mitochondria and endoplasmic reticula, where it mediates phospholipid exchange. The encoded protein plays a major role in mitochondrial function and intracellular cholesterol trafficking. Defects in this gene are a cause of 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (MEGDEL). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012]","start":158109515,"end":158168270,"strand":-1,"description":"serine active site containing 1 [Source:HGNC Symbol;Acc:HGNC:21061]"}, {"versioned_ensembl_gene_id":"ENSG00000260228.5","gene_symbol":"AC009119.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83789967,"end":83807834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261103.1","gene_symbol":"AC009063.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83710179,"end":83717898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234276.1","gene_symbol":"SDR42E1P3","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51834]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422347","summary":null,"start":62690033,"end":62690534,"strand":1,"description":"short chain dehydrogenase/reductase family 42E, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51834]"}, {"versioned_ensembl_gene_id":"ENSG00000250227.1","gene_symbol":"TRIM60P14","gene_name":"tripartite motif containing 60 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653794","summary":null,"start":164915565,"end":164916983,"strand":1,"description":"tripartite motif containing 60 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38486]"}, {"versioned_ensembl_gene_id":"ENSG00000256134.1","gene_symbol":"EGLN3P1","gene_name":"egl-9 family hypoxia-inducible factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49857]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420503","summary":null,"start":15971890,"end":15972609,"strand":-1,"description":"egl-9 family hypoxia-inducible factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49857]"}, {"versioned_ensembl_gene_id":"ENSG00000215305.9","gene_symbol":"VPS16","gene_name":"VPS16, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14584]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64601","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps16 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009]","start":2840703,"end":2866732,"strand":1,"description":"VPS16, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14584]"}, {"versioned_ensembl_gene_id":"ENSG00000232806.1","gene_symbol":"AP001610.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41559125,"end":41562958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234537.1","gene_symbol":"AL354751.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92132398,"end":92138629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249289.1","gene_symbol":"AC010460.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23329427,"end":23329892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176390.11","gene_symbol":"CRLF3","gene_name":"cytokine receptor like factor 3 [Source:HGNC Symbol;Acc:HGNC:17177]","synonyms":"CYTOR4,CREME9","biotype":"protein_coding","ncbi_id":"51379","summary":"This gene encodes a cytokine receptor-like factor that may negatively regulate cell cycle progression at the G0/G1 phase. Studies of the related rat protein suggest that it may regulate neuronal morphology and synaptic vesicle biogenesis. This gene is one of several genes located in the neurofibromatosis type I tumor suppressor region on the q arm of chromosome 17, a region that is subject to microdeletions, duplications, chromosomal breaks and rearrangements. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2 and 5. [provided by RefSeq, Aug 2012]","start":30769388,"end":30824776,"strand":-1,"description":"cytokine receptor like factor 3 [Source:HGNC Symbol;Acc:HGNC:17177]"}, {"versioned_ensembl_gene_id":"ENSG00000225957.1","gene_symbol":"AC231532.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52382053,"end":52385614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261549.2","gene_symbol":"AC107954.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88989519,"end":88990245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105717.13","gene_symbol":"PBX4","gene_name":"PBX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:13403]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80714","summary":"This gene encodes a member of the pre-B cell leukemia transcription factor family. These proteins are homeobox proteins that play critical roles in embryonic development and cellular differentiation both as Hox cofactors and through Hox-independent pathways. The encoded protein contains a homeobox DNA-binding domain, but specific functions of the protein have not been determined. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2011]","start":19561707,"end":19618916,"strand":-1,"description":"PBX homeobox 4 [Source:HGNC Symbol;Acc:HGNC:13403]"}, {"versioned_ensembl_gene_id":"ENSG00000254925.1","gene_symbol":"OR4C9P","gene_name":"olfactory receptor family 4 subfamily C member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:14796]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48464053,"end":48464977,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:14796]"}, {"versioned_ensembl_gene_id":"ENSG00000228594.3","gene_symbol":"FNDC10","gene_name":"fibronectin type III domain containing 10 [Source:HGNC Symbol;Acc:HGNC:42951]","synonyms":"C1orf233","biotype":"protein_coding","ncbi_id":"643988","summary":null,"start":1598012,"end":1600096,"strand":-1,"description":"fibronectin type III domain containing 10 [Source:HGNC Symbol;Acc:HGNC:42951]"}, {"versioned_ensembl_gene_id":"ENSG00000263342.1","gene_symbol":"AC003688.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7282947,"end":7284071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274439.2","gene_symbol":"AC136352.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":21372682,"end":21387280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008294.20","gene_symbol":"SPAG9","gene_name":"sperm associated antigen 9 [Source:HGNC Symbol;Acc:HGNC:14524]","synonyms":"JIP4,JIP-4,HSS,HLC4,FLJ34602,FLJ26141,FLJ14006,FLJ13450,CT89,SYD1,PIG6,PHET,MGC74461,MGC14967,MGC117291,KIAA0516,JLP","biotype":"protein_coding","ncbi_id":"9043","summary":"This gene encodes a member of the cancer testis antigen gene family. The encoded protein functions as a scaffold protein that structurally organizes mitogen-activated protein kinases and mediates c-Jun-terminal kinase signaling. This protein also binds to kinesin-1 and may be involved in microtubule-based membrane transport. This protein may play a role in tumor growth and development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":50962174,"end":51120865,"strand":-1,"description":"sperm associated antigen 9 [Source:HGNC Symbol;Acc:HGNC:14524]"}, {"versioned_ensembl_gene_id":"ENSG00000267450.1","gene_symbol":"OR1AB1P","gene_name":"olfactory receptor family 1 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15390]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81090","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":16051929,"end":16052689,"strand":1,"description":"olfactory receptor family 1 subfamily AB member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15390]"}, {"versioned_ensembl_gene_id":"ENSG00000229891.1","gene_symbol":"LINC01315","gene_name":"long intergenic non-protein coding RNA 1315 [Source:HGNC Symbol;Acc:HGNC:50513]","synonyms":"lnc-C22orf32-1","biotype":"lincRNA","ncbi_id":"102723775","summary":null,"start":42364400,"end":42369236,"strand":-1,"description":"long intergenic non-protein coding RNA 1315 [Source:HGNC Symbol;Acc:HGNC:50513]"}, {"versioned_ensembl_gene_id":"ENSG00000244681.1","gene_symbol":"MTHFD2P1","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48859]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100287639","summary":null,"start":95654423,"end":95683193,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48859]"}, {"versioned_ensembl_gene_id":"ENSG00000244048.1","gene_symbol":"RPS18P6","gene_name":"ribosomal protein S18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271076","summary":null,"start":95171920,"end":95172377,"strand":1,"description":"ribosomal protein S18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36028]"}, {"versioned_ensembl_gene_id":"ENSG00000258253.1","gene_symbol":"AC078865.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52380460,"end":52402407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277332.1","gene_symbol":"AC108002.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142638596,"end":142640648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213051.3","gene_symbol":"RPL5P5","gene_name":"ribosomal protein L5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35564]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730213","summary":null,"start":185226808,"end":185227700,"strand":-1,"description":"ribosomal protein L5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35564]"}, {"versioned_ensembl_gene_id":"ENSG00000203952.9","gene_symbol":"CCDC160","gene_name":"coiled-coil domain containing 160 [Source:HGNC Symbol;Acc:HGNC:37286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347475","summary":null,"start":134237047,"end":134246207,"strand":1,"description":"coiled-coil domain containing 160 [Source:HGNC Symbol;Acc:HGNC:37286]"}, {"versioned_ensembl_gene_id":"ENSG00000229331.1","gene_symbol":"GK-IT1","gene_name":"GK intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41339]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480740","summary":null,"start":30671635,"end":30672166,"strand":1,"description":"GK intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41339]"}, {"versioned_ensembl_gene_id":"ENSG00000215014.4","gene_symbol":"AL645728.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1574975,"end":1577075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274481.1","gene_symbol":"AL691432.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1583510,"end":1583909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274614.1","gene_symbol":"AL390754.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":111182111,"end":111182692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166704.11","gene_symbol":"ZNF606","gene_name":"zinc finger protein 606 [Source:HGNC Symbol;Acc:HGNC:25879]","synonyms":"ZNF328,KIAA1852,FLJ14260","biotype":"protein_coding","ncbi_id":"80095","summary":"This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) domain at its N-terminus, followed by contiguous C2H2 zinc finger motifs. The encoded protein is a nuclear protein that can act as a transcriptional repressor of growth factor-mediated signaling pathways in a reporter gene assay. This protein has been shown to interact with the SRY-box 9 gene product, and suppresses its transcriptional activity by inhibiting its DNA binding activity. Reduced expression of this gene promotes chondrocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":57977053,"end":58003349,"strand":-1,"description":"zinc finger protein 606 [Source:HGNC Symbol;Acc:HGNC:25879]"}, {"versioned_ensembl_gene_id":"ENSG00000101574.14","gene_symbol":"METTL4","gene_name":"methyltransferase like 4 [Source:HGNC Symbol;Acc:HGNC:24726]","synonyms":"HsT661,FLJ23017","biotype":"protein_coding","ncbi_id":"64863","summary":null,"start":2537525,"end":2571509,"strand":-1,"description":"methyltransferase like 4 [Source:HGNC Symbol;Acc:HGNC:24726]"}, {"versioned_ensembl_gene_id":"ENSG00000274928.6","gene_symbol":"KRT89P","gene_name":"keratin 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:30196]","synonyms":"HBB,KRTHBP2,KRT123P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"85344","summary":null,"start":52341197,"end":52354036,"strand":1,"description":"keratin 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:30196]"}, {"versioned_ensembl_gene_id":"ENSG00000143641.9","gene_symbol":"GALNT2","gene_name":"polypeptide N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4124]","synonyms":"GalNAc-T2","biotype":"protein_coding","ncbi_id":"2590","summary":"This gene encodes a member of the glycosyltransferase 2 protein family. Members of this family initiate mucin-type O-glycoslation of peptides in the Golgi apparatus. The encoded protein may be involved in O-linked glycosylation of the immunoglobulin A1 hinge region. This gene may influence triglyceride levels, and may be involved Type 2 diabetes, as well as several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":230057990,"end":230282124,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:4124]"}, {"versioned_ensembl_gene_id":"ENSG00000164500.6","gene_symbol":"C7orf72","gene_name":"chromosome 7 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:22564]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130988","summary":null,"start":50096036,"end":50159830,"strand":1,"description":"chromosome 7 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:22564]"}, {"versioned_ensembl_gene_id":"ENSG00000107874.10","gene_symbol":"CUEDC2","gene_name":"CUE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28352]","synonyms":"MGC2491,C10orf66","biotype":"protein_coding","ncbi_id":"79004","summary":null,"start":102423245,"end":102432661,"strand":-1,"description":"CUE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28352]"}, {"versioned_ensembl_gene_id":"ENSG00000122786.19","gene_symbol":"CALD1","gene_name":"caldesmon 1 [Source:HGNC Symbol;Acc:HGNC:1441]","synonyms":"CDM,L-CAD,H-CAD","biotype":"protein_coding","ncbi_id":"800","summary":"This gene encodes a calmodulin- and actin-binding protein that plays an essential role in the regulation of smooth muscle and nonmuscle contraction. The conserved domain of this protein possesses the binding activities to Ca(2+)-calmodulin, actin, tropomyosin, myosin, and phospholipids. This protein is a potent inhibitor of the actin-tropomyosin activated myosin MgATPase, and serves as a mediating factor for Ca(2+)-dependent inhibition of smooth muscle contraction. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":134744252,"end":134970728,"strand":1,"description":"caldesmon 1 [Source:HGNC Symbol;Acc:HGNC:1441]"}, {"versioned_ensembl_gene_id":"ENSG00000233148.2","gene_symbol":"SYF2P2","gene_name":"SYF2 pre-mRNA splicing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128275","summary":null,"start":35010703,"end":35011285,"strand":1,"description":"SYF2 pre-mRNA splicing factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38139]"}, {"versioned_ensembl_gene_id":"ENSG00000233399.2","gene_symbol":"LINC01648","gene_name":"long intergenic non-protein coding RNA 1648 [Source:HGNC Symbol;Acc:HGNC:52435]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929406","summary":null,"start":30013952,"end":30037612,"strand":-1,"description":"long intergenic non-protein coding RNA 1648 [Source:HGNC Symbol;Acc:HGNC:52435]"}, {"versioned_ensembl_gene_id":"ENSG00000225213.2","gene_symbol":"AC073367.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16721352,"end":16748377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259267.2","gene_symbol":"AC073176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70939053,"end":70955641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173482.16","gene_symbol":"PTPRM","gene_name":"protein tyrosine phosphatase, receptor type M [Source:HGNC Symbol;Acc:HGNC:9675]","synonyms":"hR-PTPu,RPTPU,PTPRL1","biotype":"protein_coding","ncbi_id":"5797","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP mu (MAM) domain, an Ig-like domain and four fibronectin type III-like repeats. This PTP has been shown to mediate cell-cell aggregation through the interaction with another molecule of this PTP on an adjacent cell. This PTP can interact with scaffolding protein RACK1/GNB2L1, which may be necessary for the downstream signaling in response to cell-cell adhesion. Alternative splicing results in multiple transcripts encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":7566782,"end":8406861,"strand":1,"description":"protein tyrosine phosphatase, receptor type M [Source:HGNC Symbol;Acc:HGNC:9675]"}, {"versioned_ensembl_gene_id":"ENSG00000234426.1","gene_symbol":"AL139042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88298950,"end":88421033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237082.1","gene_symbol":"COX5BP6","gene_name":"cytochrome c oxidase subunit 5B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:2275]","synonyms":"COX5BL6","biotype":"processed_pseudogene","ncbi_id":"101234262","summary":null,"start":100623875,"end":100624429,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:2275]"}, {"versioned_ensembl_gene_id":"ENSG00000141232.4","gene_symbol":"TOB1","gene_name":"transducer of ERBB2, 1 [Source:HGNC Symbol;Acc:HGNC:11979]","synonyms":"TROB1,TROB,TOB,APRO5","biotype":"protein_coding","ncbi_id":"10140","summary":"This gene encodes a member of the transducer of erbB-2 /B-cell translocation gene protein family. Members of this family are anti-proliferative factors that have the potential to regulate cell growth. The encoded protein may function as a tumor suppressor. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":50862223,"end":50867978,"strand":-1,"description":"transducer of ERBB2, 1 [Source:HGNC Symbol;Acc:HGNC:11979]"}, {"versioned_ensembl_gene_id":"ENSG00000149124.10","gene_symbol":"GLYAT","gene_name":"glycine-N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:13734]","synonyms":"GAT,ACGNAT","biotype":"protein_coding","ncbi_id":"10249","summary":"The glycine-N-acyltransferase protein conjugates glycine with acyl-CoA substrates in the mitochondria. The protein is thought to be important in the detoxification of endogenous and xenobiotic acyl-CoA's. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":58640426,"end":58731974,"strand":-1,"description":"glycine-N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:13734]"}, {"versioned_ensembl_gene_id":"ENSG00000258926.1","gene_symbol":"AL355916.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61537508,"end":61545287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279565.1","gene_symbol":"AL121835.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":88172261,"end":88175762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173714.7","gene_symbol":"WFIKKN2","gene_name":"WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30916]","synonyms":"WFIKKNRP,WFDC20B","biotype":"protein_coding","ncbi_id":"124857","summary":"The WFIKKN1 protein contains a WAP domain, follistatin domain, immunoglobulin domain, two tandem Kunitz domains, and an NTR domain. This gene encodes a WFIKKN1-related protein which has the same domain organization as the WFIKKN1 protein. The WAP-type, follistatin type, Kunitz-type, and NTR-type protease inhibitory domains may control the action of multiple types of proteases. [provided by RefSeq, Jul 2008]","start":50834650,"end":50842348,"strand":1,"description":"WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30916]"}, {"versioned_ensembl_gene_id":"ENSG00000225198.1","gene_symbol":"SSXP3","gene_name":"SSX family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30640]","synonyms":"psiSSX3","biotype":"unprocessed_pseudogene","ncbi_id":"326341","summary":null,"start":48156367,"end":48166350,"strand":1,"description":"SSX family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30640]"}, {"versioned_ensembl_gene_id":"ENSG00000262962.1","gene_symbol":"KARSP3","gene_name":"lysyl-tRNA synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39209]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132079","summary":null,"start":68002432,"end":68004952,"strand":-1,"description":"lysyl-tRNA synthetase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39209]"}, {"versioned_ensembl_gene_id":"ENSG00000198283.2","gene_symbol":"OR5B21","gene_name":"olfactory receptor family 5 subfamily B member 21 [Source:HGNC Symbol;Acc:HGNC:19616]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219968","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58507175,"end":58508105,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 21 [Source:HGNC Symbol;Acc:HGNC:19616]"}, {"versioned_ensembl_gene_id":"ENSG00000214803.3","gene_symbol":"AC090921.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124192671,"end":124247398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235271.5","gene_symbol":"LINC01422","gene_name":"long intergenic non-protein coding RNA 1422 [Source:NCBI gene;Acc:101929539]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929539","summary":null,"start":26903292,"end":26920611,"strand":1,"description":"long intergenic non-protein coding RNA 1422 [Source:NCBI gene;Acc:101929539]"}, {"versioned_ensembl_gene_id":"ENSG00000168610.14","gene_symbol":"STAT3","gene_name":"signal transducer and activator of transcription 3 [Source:HGNC Symbol;Acc:HGNC:11364]","synonyms":"APRF","biotype":"protein_coding","ncbi_id":"6774","summary":"The protein encoded by this gene is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated through phosphorylation in response to various cytokines and growth factors including IFNs, EGF, IL5, IL6, HGF, LIF and BMP2. This protein mediates the expression of a variety of genes in response to cell stimuli, and thus plays a key role in many cellular processes such as cell growth and apoptosis. The small GTPase Rac1 has been shown to bind and regulate the activity of this protein. PIAS3 protein is a specific inhibitor of this protein. This gene also plays a role in regulating host response to viral and bacterial infections. Mutations in this gene are associated with infantile-onset multisystem autoimmune disease and hyper-immunoglobulin E syndrome. [provided by RefSeq, Aug 2020]","start":42313324,"end":42388568,"strand":-1,"description":"signal transducer and activator of transcription 3 [Source:HGNC Symbol;Acc:HGNC:11364]"}, {"versioned_ensembl_gene_id":"ENSG00000223704.1","gene_symbol":"LINC01422","gene_name":"long intergenic non-protein coding RNA 1422 [Source:HGNC Symbol;Acc:HGNC:50728]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929539","summary":null,"start":26858634,"end":26865786,"strand":1,"description":"long intergenic non-protein coding RNA 1422 [Source:HGNC Symbol;Acc:HGNC:50728]"}, {"versioned_ensembl_gene_id":"ENSG00000278963.1","gene_symbol":"AC005921.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50722074,"end":50724224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213363.4","gene_symbol":"RPS3P6","gene_name":"ribosomal protein S3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36061]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645000","summary":null,"start":62021570,"end":62022174,"strand":-1,"description":"ribosomal protein S3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36061]"}, {"versioned_ensembl_gene_id":"ENSG00000226973.1","gene_symbol":"AL512638.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":115471941,"end":115476027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164292.12","gene_symbol":"RHOBTB3","gene_name":"Rho related BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18757]","synonyms":"KIAA0878","biotype":"protein_coding","ncbi_id":"22836","summary":"RHOBTB3 is a member of the evolutionarily conserved RHOBTB subfamily of Rho GTPases. For background information on RHOBTBs, see RHOBTB1 (MIM 607351).[supplied by OMIM, Apr 2004]","start":95713522,"end":95824383,"strand":1,"description":"Rho related BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18757]"}, {"versioned_ensembl_gene_id":"ENSG00000260420.2","gene_symbol":"LINC02182","gene_name":"long intergenic non-protein coding RNA 2182 [Source:HGNC Symbol;Acc:HGNC:53044]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928880","summary":null,"start":88194281,"end":88195217,"strand":1,"description":"long intergenic non-protein coding RNA 2182 [Source:HGNC Symbol;Acc:HGNC:53044]"}, {"versioned_ensembl_gene_id":"ENSG00000151615.3","gene_symbol":"POU4F2","gene_name":"POU class 4 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9219]","synonyms":"BRN3B,Brn-3b","biotype":"protein_coding","ncbi_id":"5458","summary":"The protein encoded by this gene is a member of the POU-domain transcription factor family and may be involved in maintaining visual system neurons in the retina. The level of the encoded protein is also elevated in a majority of breast cancers, resulting in accelerated tumor growth. [provided by RefSeq, Sep 2011]","start":146638893,"end":146642474,"strand":1,"description":"POU class 4 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9219]"}, {"versioned_ensembl_gene_id":"ENSG00000176732.6","gene_symbol":"PFN4","gene_name":"profilin family member 4 [Source:HGNC Symbol;Acc:HGNC:31103]","synonyms":null,"biotype":"protein_coding","ncbi_id":"375189","summary":null,"start":24115371,"end":24123477,"strand":-1,"description":"profilin family member 4 [Source:HGNC Symbol;Acc:HGNC:31103]"}, {"versioned_ensembl_gene_id":"ENSG00000267106.5","gene_symbol":"ZNF561-AS1","gene_name":"ZNF561 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27613]","synonyms":"C19orf82","biotype":"processed_transcript","ncbi_id":"284385","summary":null,"start":9621291,"end":9645896,"strand":1,"description":"ZNF561 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27613]"}, {"versioned_ensembl_gene_id":"ENSG00000162512.15","gene_symbol":"SDC3","gene_name":"syndecan 3 [Source:HGNC Symbol;Acc:HGNC:10660]","synonyms":"SYND3,N-syndecan","biotype":"protein_coding","ncbi_id":"9672","summary":"The protein encoded by this gene belongs to the syndecan proteoglycan family. It may play a role in the organization of cell shape by affecting the actin cytoskeleton, possibly by transferring signals from the cell surface in a sugar-dependent mechanism. Allelic variants of this gene have been associated with obesity. [provided by RefSeq, Oct 2009]","start":30869467,"end":30908761,"strand":-1,"description":"syndecan 3 [Source:HGNC Symbol;Acc:HGNC:10660]"}, {"versioned_ensembl_gene_id":"ENSG00000168078.9","gene_symbol":"PBK","gene_name":"PDZ binding kinase [Source:HGNC Symbol;Acc:HGNC:18282]","synonyms":"TOPK,SPK,Nori-3,FLJ14385,CT84","biotype":"protein_coding","ncbi_id":"55872","summary":"This gene encodes a serine/threonine protein kinase related to the dual specific mitogen-activated protein kinase kinase (MAPKK) family. Evidence suggests that mitotic phosphorylation is required for its catalytic activity. The encoded protein may be involved in the activation of lymphoid cells and support testicular functions, with a suggested role in the process of spermatogenesis. Overexpression of this gene has been implicated in tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":27809620,"end":27838095,"strand":-1,"description":"PDZ binding kinase [Source:HGNC Symbol;Acc:HGNC:18282]"}, {"versioned_ensembl_gene_id":"ENSG00000283541.1","gene_symbol":"BX005040.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61063752,"end":61113954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248739.1","gene_symbol":"AC069306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170141292,"end":170142532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248822.1","gene_symbol":"APOBEC3AP1","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43835]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105377532","summary":null,"start":170099818,"end":170100104,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43835]"}, {"versioned_ensembl_gene_id":"ENSG00000163719.19","gene_symbol":"MTMR14","gene_name":"myotubularin related protein 14 [Source:HGNC Symbol;Acc:HGNC:26190]","synonyms":"FLJ90311,FLJ22405,C3orf29,hJumpy,hEDTP","biotype":"protein_coding","ncbi_id":"64419","summary":"This gene encodes a myotubularin-related protein. The encoded protein is a phosphoinositide phosphatase that specifically dephosphorylates phosphatidylinositol 3,5-biphosphate and phosphatidylinositol 3-phosphate. Mutations in this gene are correlated with autosomal dominant centronuclear myopathy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 18.[provided by RefSeq, Apr 2010]","start":9649433,"end":9702393,"strand":1,"description":"myotubularin related protein 14 [Source:HGNC Symbol;Acc:HGNC:26190]"}, {"versioned_ensembl_gene_id":"ENSG00000255431.1","gene_symbol":"OR5B19P","gene_name":"olfactory receptor family 5 subfamily B member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81211","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58343737,"end":58344664,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15269]"}, {"versioned_ensembl_gene_id":"ENSG00000259038.1","gene_symbol":"AL121820.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68627166,"end":68628445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164904.17","gene_symbol":"ALDH7A1","gene_name":"aldehyde dehydrogenase 7 family member A1 [Source:HGNC Symbol;Acc:HGNC:877]","synonyms":"EPD,ATQ1,PDE","biotype":"protein_coding","ncbi_id":"501","summary":"The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified. [provided by RefSeq, Jan 2011]","start":126531200,"end":126595418,"strand":-1,"description":"aldehyde dehydrogenase 7 family member A1 [Source:HGNC Symbol;Acc:HGNC:877]"}, {"versioned_ensembl_gene_id":"ENSG00000234949.2","gene_symbol":"AC104667.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":237591020,"end":237595981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237705.1","gene_symbol":"AC008937.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56842016,"end":56862164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279397.1","gene_symbol":"AC018445.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79515798,"end":79516057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232940.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"antisense_RNA","ncbi_id":"414765","summary":null,"start":33249534,"end":33254989,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000243062.5","gene_symbol":"AL359853.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179730217,"end":179742697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268074.1","gene_symbol":"AC246680.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143929994,"end":143930382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273711.1","gene_symbol":"AC005520.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73885392,"end":73885555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277882.1","gene_symbol":"AL592295.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161411597,"end":161411802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283696.1","gene_symbol":"AL592295.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161399409,"end":161422424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271724.1","gene_symbol":"AC011396.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":146375591,"end":146376219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234136.1","gene_symbol":"AC055764.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197830685,"end":197831296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236484.2","gene_symbol":"RRM2P2","gene_name":"ribonucleotide reductase M2 polypeptide pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"6244","summary":null,"start":161378707,"end":161379358,"strand":-1,"description":"ribonucleotide reductase M2 polypeptide pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10454]"}, {"versioned_ensembl_gene_id":"ENSG00000091010.4","gene_symbol":"POU4F3","gene_name":"POU class 4 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:9220]","synonyms":"DFNA52,DFNA42,DFNA15,BRN3C","biotype":"protein_coding","ncbi_id":"5459","summary":"This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009]","start":146339024,"end":146340520,"strand":1,"description":"POU class 4 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:9220]"}, {"versioned_ensembl_gene_id":"ENSG00000267079.1","gene_symbol":"AP001269.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11910634,"end":11914344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187741.14","gene_symbol":"FANCA","gene_name":"Fanconi anemia complementation group A [Source:HGNC Symbol;Acc:HGNC:3582]","synonyms":"FAA,FA-H,FANCH,FAH,FACA","biotype":"protein_coding","ncbi_id":"2175","summary":"The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008]","start":89737549,"end":89816657,"strand":-1,"description":"Fanconi anemia complementation group A [Source:HGNC Symbol;Acc:HGNC:3582]"}, {"versioned_ensembl_gene_id":"ENSG00000272569.1","gene_symbol":"AP004247.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58171098,"end":58171721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267457.1","gene_symbol":"AC004223.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35073831,"end":35074374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168077.13","gene_symbol":"SCARA3","gene_name":"scavenger receptor class A member 3 [Source:HGNC Symbol;Acc:HGNC:19000]","synonyms":"MSRL1,MSLR1,CSR1,CSR,APC7","biotype":"protein_coding","ncbi_id":"51435","summary":"This gene encodes a macrophage scavenger receptor-like protein. This protein has been shown to deplete reactive oxygen species, and thus play an important role in protecting cells from oxidative stress. The expression of this gene is induced by oxidative stress. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":27633868,"end":27676776,"strand":1,"description":"scavenger receptor class A member 3 [Source:HGNC Symbol;Acc:HGNC:19000]"}, {"versioned_ensembl_gene_id":"ENSG00000254422.1","gene_symbol":"AP000942.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102229851,"end":102230922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183146.4","gene_symbol":"PRORY","gene_name":"proline rich, Y-linked [Source:HGNC Symbol;Acc:HGNC:38732]","synonyms":"CYorf17","biotype":"protein_coding","ncbi_id":"100533178","summary":null,"start":21382954,"end":21386360,"strand":-1,"description":"proline rich, Y-linked [Source:HGNC Symbol;Acc:HGNC:38732]"}, {"versioned_ensembl_gene_id":"ENSG00000226918.1","gene_symbol":"AC010086.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21311268,"end":21318895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124813.20","gene_symbol":"RUNX2","gene_name":"runt related transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10472]","synonyms":"PEBP2aA1,PEBP2A1,CCD1,CCD,CBFA1,AML3","biotype":"protein_coding","ncbi_id":"860","summary":"This gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Two regions of potential trinucleotide repeat expansions are present in the N-terminal region of the encoded protein, and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Jul 2016]","start":45328157,"end":45664349,"strand":1,"description":"runt related transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10472]"}, {"versioned_ensembl_gene_id":"ENSG00000227169.2","gene_symbol":"Z98747.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4551735,"end":4552145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217228.1","gene_symbol":"GSTA12P","gene_name":"glutathione S-transferase alpha 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:49906]","synonyms":"GSTAP5","biotype":"unprocessed_pseudogene","ncbi_id":"647169","summary":null,"start":52765280,"end":52778347,"strand":-1,"description":"glutathione S-transferase alpha 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:49906]"}, {"versioned_ensembl_gene_id":"ENSG00000074706.13","gene_symbol":"IPCEF1","gene_name":"interaction protein for cytohesin exchange factors 1 [Source:HGNC Symbol;Acc:HGNC:21204]","synonyms":"PIP3-E,KIAA0403","biotype":"protein_coding","ncbi_id":"26034","summary":null,"start":154154496,"end":154356792,"strand":-1,"description":"interaction protein for cytohesin exchange factors 1 [Source:HGNC Symbol;Acc:HGNC:21204]"}, {"versioned_ensembl_gene_id":"ENSG00000204116.11","gene_symbol":"CHIC1","gene_name":"cysteine rich hydrophobic domain 1 [Source:HGNC Symbol;Acc:HGNC:1934]","synonyms":"BRX","biotype":"protein_coding","ncbi_id":"53344","summary":"This gene encodes a cysteine-rich hydrophobic (CHIC) domain-containing protein, and is one of the few protein-coding genes found near the X-inactivation center. Studies in mouse indicate that the mouse ortholog of this gene is subject to X-inactivation in mouse. Experiments with other CHIC domain-containing family members show that the cysteine residues are palmitoylated post-translationally, resulting in membrane association. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017]","start":73563200,"end":73687102,"strand":1,"description":"cysteine rich hydrophobic domain 1 [Source:HGNC Symbol;Acc:HGNC:1934]"}, {"versioned_ensembl_gene_id":"ENSG00000260112.1","gene_symbol":"AC008567.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9518150,"end":9519341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250547.1","gene_symbol":"AC079238.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163265575,"end":163266583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229931.1","gene_symbol":"AL137003.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16761138,"end":16762652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125534.9","gene_symbol":"PPDPF","gene_name":"pancreatic progenitor cell differentiation and proliferation factor [Source:HGNC Symbol;Acc:HGNC:16142]","synonyms":"exdpf,dJ697K14.9,C20orf149","biotype":"protein_coding","ncbi_id":"79144","summary":null,"start":63520724,"end":63522206,"strand":1,"description":"pancreatic progenitor cell differentiation and proliferation factor [Source:HGNC Symbol;Acc:HGNC:16142]"}, {"versioned_ensembl_gene_id":"ENSG00000258649.1","gene_symbol":"AL392023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38190983,"end":38202923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272455.1","gene_symbol":"AL391244.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1409096,"end":1410618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126215.13","gene_symbol":"XRCC3","gene_name":"X-ray repair cross complementing 3 [Source:HGNC Symbol;Acc:HGNC:12830]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7517","summary":"This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene functionally complements Chinese hamster irs1SF, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents and is chromosomally unstable. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":103697609,"end":103715504,"strand":-1,"description":"X-ray repair cross complementing 3 [Source:HGNC Symbol;Acc:HGNC:12830]"}, {"versioned_ensembl_gene_id":"ENSG00000106261.16","gene_symbol":"ZKSCAN1","gene_name":"zinc finger with KRAB and SCAN domains 1 [Source:HGNC Symbol;Acc:HGNC:13101]","synonyms":"ZSCAN33,ZNF36,ZNF139,PHZ-37,KOX18","biotype":"protein_coding","ncbi_id":"7586","summary":"This gene encodes a member of the Kruppel C2H2-type zinc-finger family of proteins. This encoded protein may function as a transcription factor that regulates the expression of GABA type-A receptors in the brain. Transcripts from this gene have been shown to form stable and abundant circular RNAs. Elevated expression of this gene has been observed in gastric cancer and the encoded protein may stimulate migration and invasion of human gastric cancer cells. [provided by RefSeq, Oct 2016]","start":100015572,"end":100041689,"strand":1,"description":"zinc finger with KRAB and SCAN domains 1 [Source:HGNC Symbol;Acc:HGNC:13101]"}, {"versioned_ensembl_gene_id":"ENSG00000185296.8","gene_symbol":"AC026785.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17306381,"end":17306960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265579.1","gene_symbol":"AC023301.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":72743756,"end":72745961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243197.7","gene_symbol":"TUSC7","gene_name":"tumor suppressor candidate 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27701]","synonyms":"NCRNA00295,LSAMP-AS3,LOC285194,LINC00902","biotype":"antisense_RNA","ncbi_id":"285194","summary":null,"start":116709235,"end":116723581,"strand":1,"description":"tumor suppressor candidate 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27701]"}, {"versioned_ensembl_gene_id":"ENSG00000266997.2","gene_symbol":"AC090227.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49795793,"end":49837623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164045.11","gene_symbol":"CDC25A","gene_name":"cell division cycle 25A [Source:HGNC Symbol;Acc:HGNC:1725]","synonyms":null,"biotype":"protein_coding","ncbi_id":"993","summary":"CDC25A is a member of the CDC25 family of phosphatases. CDC25A is required for progression from G1 to the S phase of the cell cycle. It activates the cyclin-dependent kinase CDC2 by removing two phosphate groups. CDC25A is specifically degraded in response to DNA damage, which prevents cells with chromosomal abnormalities from progressing through cell division. CDC25A is an oncogene, although its exact role in oncogenesis has not been demonstrated. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":48157146,"end":48188402,"strand":-1,"description":"cell division cycle 25A [Source:HGNC Symbol;Acc:HGNC:1725]"}, {"versioned_ensembl_gene_id":"ENSG00000232036.2","gene_symbol":"AL078645.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184566511,"end":184567835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260008.1","gene_symbol":"AP001527.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102107886,"end":102109842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069998.12","gene_symbol":"HDHD5","gene_name":"haloacid dehalogenase like hydrolase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:1843]","synonyms":"CECR5","biotype":"protein_coding","ncbi_id":"27440","summary":null,"start":17137511,"end":17165287,"strand":-1,"description":"haloacid dehalogenase like hydrolase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:1843]"}, {"versioned_ensembl_gene_id":"ENSG00000236871.7","gene_symbol":"LINC00106","gene_name":"long intergenic non-protein coding RNA 106 [Source:HGNC Symbol;Acc:HGNC:31843]","synonyms":"OTTHUMG00000021061,NCRNA00106,CXYorf8","biotype":"lincRNA","ncbi_id":"751580","summary":null,"start":1396427,"end":1399402,"strand":1,"description":"long intergenic non-protein coding RNA 106 [Source:HGNC Symbol;Acc:HGNC:31843]"}, {"versioned_ensembl_gene_id":"ENSG00000255531.1","gene_symbol":"NDUFS5P6","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480785","summary":null,"start":67849044,"end":67849338,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44044]"}, {"versioned_ensembl_gene_id":"ENSG00000264475.1","gene_symbol":"AP005062.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7076817,"end":7080123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105186.15","gene_symbol":"ANKRD27","gene_name":"ankyrin repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:25310]","synonyms":"VARP,FLJ00040,DKFZp434L0718","biotype":"protein_coding","ncbi_id":"84079","summary":null,"start":32597007,"end":32676597,"strand":-1,"description":"ankyrin repeat domain 27 [Source:HGNC Symbol;Acc:HGNC:25310]"}, {"versioned_ensembl_gene_id":"ENSG00000258819.1","gene_symbol":"LINC02289","gene_name":"long intergenic non-protein coding RNA 2289 [Source:HGNC Symbol;Acc:HGNC:53205]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724190","summary":null,"start":77069180,"end":77076344,"strand":-1,"description":"long intergenic non-protein coding RNA 2289 [Source:HGNC Symbol;Acc:HGNC:53205]"}, {"versioned_ensembl_gene_id":"ENSG00000226923.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31516169,"end":31517684,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000261612.1","gene_symbol":"SUB1P3","gene_name":"SUB1 homolog, transcriptional regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43993]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480442","summary":null,"start":4562814,"end":4563128,"strand":-1,"description":"SUB1 homolog, transcriptional regulator pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43993]"}, {"versioned_ensembl_gene_id":"ENSG00000197753.8","gene_symbol":"LHFPL5","gene_name":"LHFPL tetraspan subfamily member 5 [Source:HGNC Symbol;Acc:HGNC:21253]","synonyms":"Tmhs,MGC33835,dJ510O8.8,DFNB67","biotype":"protein_coding","ncbi_id":"222662","summary":"This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis. [provided by RefSeq, Jul 2008]","start":35805293,"end":35833874,"strand":1,"description":"LHFPL tetraspan subfamily member 5 [Source:HGNC Symbol;Acc:HGNC:21253]"}, {"versioned_ensembl_gene_id":"ENSG00000249506.3","gene_symbol":"ZEB2P1","gene_name":"zinc finger E-box binding homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33346]","synonyms":"ZEB1P1","biotype":"transcribed_processed_pseudogene","ncbi_id":"100420926","summary":null,"start":16360686,"end":16397323,"strand":-1,"description":"zinc finger E-box binding homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33346]"}, {"versioned_ensembl_gene_id":"ENSG00000138772.12","gene_symbol":"ANXA3","gene_name":"annexin A3 [Source:HGNC Symbol;Acc:HGNC:541]","synonyms":"ANX3","biotype":"protein_coding","ncbi_id":"306","summary":"This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. This protein functions in the inhibition of phopholipase A2 and cleavage of inositol 1,2-cyclic phosphate to form inositol 1-phosphate. This protein may also play a role in anti-coagulation. [provided by RefSeq, Jul 2008]","start":78551519,"end":78610451,"strand":1,"description":"annexin A3 [Source:HGNC Symbol;Acc:HGNC:541]"}, {"versioned_ensembl_gene_id":"ENSG00000232471.3","gene_symbol":"AC119751.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49550032,"end":49557400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262302.1","gene_symbol":"AC003688.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7246829,"end":7262089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251436.2","gene_symbol":"NUP58P1","gene_name":"nucleoporin 58 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44052]","synonyms":"NUPL1P1","biotype":"processed_pseudogene","ncbi_id":"100289295","summary":null,"start":125681177,"end":125683668,"strand":-1,"description":"nucleoporin 58 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44052]"}, {"versioned_ensembl_gene_id":"ENSG00000224740.8","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30806191,"end":30820021,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000196431.3","gene_symbol":"CRYBA4","gene_name":"crystallin beta A4 [Source:HGNC Symbol;Acc:HGNC:2396]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1413","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta acidic group member, is part of a gene cluster with beta-B1, beta-B2, and beta-B3. [provided by RefSeq, Jul 2008]","start":26621964,"end":26630672,"strand":1,"description":"crystallin beta A4 [Source:HGNC Symbol;Acc:HGNC:2396]"}, {"versioned_ensembl_gene_id":"ENSG00000258962.2","gene_symbol":"AL121839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91709111,"end":91710617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071054.16","gene_symbol":"MAP4K4","gene_name":"mitogen-activated protein kinase kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6866]","synonyms":"NIK,HGK,FLH21957","biotype":"protein_coding","ncbi_id":"9448","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase has been shown to specifically activate MAPK8/JNK. The activation of MAPK8 by this kinase is found to be inhibited by the dominant-negative mutants of MAP3K7/TAK1, MAP2K4/MKK4, and MAP2K7/MKK7, which suggests that this kinase may function through the MAP3K7-MAP2K4-MAP2K7 kinase cascade, and mediate the TNF-alpha signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":101696850,"end":101894689,"strand":1,"description":"mitogen-activated protein kinase kinase kinase kinase 4 [Source:HGNC Symbol;Acc:HGNC:6866]"}, {"versioned_ensembl_gene_id":"ENSG00000267734.1","gene_symbol":"AL121989.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86932199,"end":86934891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259383.1","gene_symbol":"AC012414.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20759311,"end":20774794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250618.1","gene_symbol":"AC023141.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57817996,"end":57818197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198406.7","gene_symbol":"BZW1P2","gene_name":"basic leucine zipper and W2 domains 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33954]","synonyms":"BZW1L1","biotype":"processed_pseudogene","ncbi_id":"151579","summary":null,"start":116645902,"end":116646727,"strand":-1,"description":"basic leucine zipper and W2 domains 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33954]"}, {"versioned_ensembl_gene_id":"ENSG00000251158.1","gene_symbol":"AC131392.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69898867,"end":69903198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225568.1","gene_symbol":"AC093155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87045875,"end":87046700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273375.1","gene_symbol":"AC055764.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197789700,"end":197790369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265614.1","gene_symbol":"AC011193.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34331862,"end":34332228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253507.5","gene_symbol":"AC104257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131308545,"end":131317632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259982.1","gene_symbol":"AC145285.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28700294,"end":28701540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258854.1","gene_symbol":"AL358333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51982520,"end":51987219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136842.13","gene_symbol":"TMOD1","gene_name":"tropomodulin 1 [Source:HGNC Symbol;Acc:HGNC:11871]","synonyms":"TMOD,ETMOD,D9S57E","biotype":"protein_coding","ncbi_id":"7111","summary":"This gene encodes a member of the tropomodulin family. The encoded protein is an actin-capping protein that regulates tropomyosin by binding to its N-terminus, inhibiting depolymerization and elongation of the pointed end of actin filaments and thereby influencing the structure of the erythrocyte membrane skeleton. Multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2009]","start":97501180,"end":97601748,"strand":1,"description":"tropomodulin 1 [Source:HGNC Symbol;Acc:HGNC:11871]"}, {"versioned_ensembl_gene_id":"ENSG00000225072.1","gene_symbol":"OR7E116P","gene_name":"olfactory receptor family 7 subfamily E member 116 pseudogene [Source:HGNC Symbol;Acc:HGNC:15122]","synonyms":"OST733","biotype":"unprocessed_pseudogene","ncbi_id":"81358","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":90232185,"end":90233141,"strand":1,"description":"olfactory receptor family 7 subfamily E member 116 pseudogene [Source:HGNC Symbol;Acc:HGNC:15122]"}, {"versioned_ensembl_gene_id":"ENSG00000075790.10","gene_symbol":"BCAP29","gene_name":"B-cell receptor associated protein 29 [Source:HGNC Symbol;Acc:HGNC:24131]","synonyms":"DKFZp686M2086,BAP29","biotype":"protein_coding","ncbi_id":"55973","summary":null,"start":107579977,"end":107629170,"strand":1,"description":"B-cell receptor associated protein 29 [Source:HGNC Symbol;Acc:HGNC:24131]"}, {"versioned_ensembl_gene_id":"ENSG00000220240.1","gene_symbol":"AL157777.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":86897547,"end":86897683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219190.1","gene_symbol":"AL353133.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86768522,"end":86768932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229152.2","gene_symbol":"ANKRD10-IT1","gene_name":"ANKRD10 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39891]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100505494","summary":null,"start":110894639,"end":110899172,"strand":-1,"description":"ANKRD10 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39891]"}, {"versioned_ensembl_gene_id":"ENSG00000274605.1","gene_symbol":"AL355338.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100086031,"end":100088848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280936.1","gene_symbol":"AL353658.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63422269,"end":63424555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226390.1","gene_symbol":"AL353658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63448051,"end":63449329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229236.1","gene_symbol":"TTTY10","gene_name":"testis-specific transcript, Y-linked 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18491]","synonyms":"NCRNA00133","biotype":"lincRNA","ncbi_id":"246119","summary":null,"start":20465668,"end":20519228,"strand":-1,"description":"testis-specific transcript, Y-linked 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18491]"}, {"versioned_ensembl_gene_id":"ENSG00000264127.1","gene_symbol":"SCML2P1","gene_name":"SCML2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421167","summary":null,"start":6926944,"end":6928210,"strand":1,"description":"SCML2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44329]"}, {"versioned_ensembl_gene_id":"ENSG00000262031.1","gene_symbol":"LINC01974","gene_name":"long intergenic non-protein coding RNA 1974 [Source:HGNC Symbol;Acc:HGNC:52801]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371798","summary":null,"start":46909742,"end":46911512,"strand":-1,"description":"long intergenic non-protein coding RNA 1974 [Source:HGNC Symbol;Acc:HGNC:52801]"}, {"versioned_ensembl_gene_id":"ENSG00000211725.3","gene_symbol":"TRBV5-5","gene_name":"T-cell receptor beta variable 5-5 [Source:HGNC Symbol;Acc:HGNC:12222]","synonyms":"TRBV55,TCRBV5S5,TCRBV5S3A2T","biotype":"TR_V_gene","ncbi_id":"28610","summary":null,"start":142482548,"end":142483019,"strand":1,"description":"T-cell receptor beta variable 5-5 [Source:HGNC Symbol;Acc:HGNC:12222]"}, {"versioned_ensembl_gene_id":"ENSG00000232913.7","gene_symbol":"PLCE1-AS2","gene_name":"PLCE1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51206]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927049","summary":null,"start":94081950,"end":94108814,"strand":-1,"description":"PLCE1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51206]"}, {"versioned_ensembl_gene_id":"ENSG00000253362.1","gene_symbol":"AC012400.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84163449,"end":84164564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233993.1","gene_symbol":"AL121900.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18674395,"end":18698709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253934.2","gene_symbol":"MRPL49P2","gene_name":"mitochondrial ribosomal protein L49 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"346711","summary":null,"start":16374618,"end":16375082,"strand":1,"description":"mitochondrial ribosomal protein L49 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29718]"}, {"versioned_ensembl_gene_id":"ENSG00000178193.5","gene_symbol":"AL357314.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75710003,"end":75724011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254195.1","gene_symbol":"TPM3P3","gene_name":"tropomyosin 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39166]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478937","summary":null,"start":84162118,"end":84162471,"strand":1,"description":"tropomyosin 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39166]"}, {"versioned_ensembl_gene_id":"ENSG00000260805.2","gene_symbol":"AC092803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212557833,"end":212559731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214434.2","gene_symbol":"NIFKP1","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44949]","synonyms":"MKI67IPP1","biotype":"processed_pseudogene","ncbi_id":"401825","summary":null,"start":30380174,"end":30381062,"strand":1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44949]"}, {"versioned_ensembl_gene_id":"ENSG00000268713.1","gene_symbol":"AC005261.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57261354,"end":57262738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163046.15","gene_symbol":"ANKRD30BL","gene_name":"ankyrin repeat domain 30B like [Source:HGNC Symbol;Acc:HGNC:35167]","synonyms":"NCRNA00164,ANKRD30BP3","biotype":"protein_coding","ncbi_id":"554226","summary":null,"start":132147591,"end":132257969,"strand":-1,"description":"ankyrin repeat domain 30B like [Source:HGNC Symbol;Acc:HGNC:35167]"}, {"versioned_ensembl_gene_id":"ENSG00000158604.14","gene_symbol":"TMED4","gene_name":"transmembrane p24 trafficking protein 4 [Source:HGNC Symbol;Acc:HGNC:22301]","synonyms":"p24alpha3,p24a3,HNLF","biotype":"protein_coding","ncbi_id":"222068","summary":null,"start":44577894,"end":44582287,"strand":-1,"description":"transmembrane p24 trafficking protein 4 [Source:HGNC Symbol;Acc:HGNC:22301]"}, {"versioned_ensembl_gene_id":"ENSG00000173467.8","gene_symbol":"AGR3","gene_name":"anterior gradient 3, protein disulphide isomerase family member [Source:HGNC Symbol;Acc:HGNC:24167]","synonyms":"PDIA18,HAG3,hAG-3,BCMP11","biotype":"protein_coding","ncbi_id":"155465","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, and a C-terminal ER-retention sequence. This gene is expressed in ciliated airway epithelial cells and, in mouse, plays a role in ciliary beat frequency in multiciliated cells. This gene is also over-expressed in breast, ovarian, and prostrate cancers. [provided by RefSeq, Dec 2016]","start":16859405,"end":16881987,"strand":-1,"description":"anterior gradient 3, protein disulphide isomerase family member [Source:HGNC Symbol;Acc:HGNC:24167]"}, {"versioned_ensembl_gene_id":"ENSG00000268379.1","gene_symbol":"AC025588.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57175233,"end":57177921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280460.1","gene_symbol":"AC006359.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":144660404,"end":144669313,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270226.1","gene_symbol":"AC006548.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17012404,"end":17012932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250735.5","gene_symbol":"AC096759.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75401195,"end":75423023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261188.1","gene_symbol":"Z95115.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26512537,"end":26514568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167094.15","gene_symbol":"TTC16","gene_name":"tetratricopeptide repeat domain 16 [Source:HGNC Symbol;Acc:HGNC:26536]","synonyms":"FLJ32780","biotype":"protein_coding","ncbi_id":"158248","summary":null,"start":127716066,"end":127731600,"strand":1,"description":"tetratricopeptide repeat domain 16 [Source:HGNC Symbol;Acc:HGNC:26536]"}, {"versioned_ensembl_gene_id":"ENSG00000156030.13","gene_symbol":"ELMSAN1","gene_name":"ELM2 and Myb/SANT domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19853]","synonyms":"LSR68,C14orf43,C14orf117","biotype":"protein_coding","ncbi_id":"91748","summary":null,"start":73715122,"end":73790285,"strand":-1,"description":"ELM2 and Myb/SANT domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19853]"}, {"versioned_ensembl_gene_id":"ENSG00000224464.2","gene_symbol":"PGAM1P6","gene_name":"phosphoglycerate mutase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42453]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420567","summary":null,"start":23872268,"end":23873014,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42453]"}, {"versioned_ensembl_gene_id":"ENSG00000151458.11","gene_symbol":"ANKRD50","gene_name":"ankyrin repeat domain 50 [Source:HGNC Symbol;Acc:HGNC:29223]","synonyms":"KIAA1223","biotype":"protein_coding","ncbi_id":"57182","summary":null,"start":124664052,"end":124712732,"strand":-1,"description":"ankyrin repeat domain 50 [Source:HGNC Symbol;Acc:HGNC:29223]"}, {"versioned_ensembl_gene_id":"ENSG00000089486.16","gene_symbol":"CDIP1","gene_name":"cell death inducing p53 target 1 [Source:HGNC Symbol;Acc:HGNC:13234]","synonyms":"LITAFL,CDIP,C16orf5","biotype":"protein_coding","ncbi_id":"29965","summary":null,"start":4510675,"end":4538828,"strand":-1,"description":"cell death inducing p53 target 1 [Source:HGNC Symbol;Acc:HGNC:13234]"}, {"versioned_ensembl_gene_id":"ENSG00000237754.1","gene_symbol":"AC093655.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68241637,"end":68242267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226829.1","gene_symbol":"AC093655.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68150283,"end":68288233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225209.1","gene_symbol":"AC092637.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68020253,"end":68032690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279026.1","gene_symbol":"AC005225.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73580694,"end":73582918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221978.11","gene_symbol":"CCNL2","gene_name":"cyclin L2 [Source:HGNC Symbol;Acc:HGNC:20570]","synonyms":"SB138,PCEE,HLA-ISO,CCNS,CCNM,ania-6b","biotype":"protein_coding","ncbi_id":"81669","summary":"The protein encoded by this gene belongs to the cyclin family. Through its interaction with several proteins, such as RNA polymerase II, splicing factors, and cyclin-dependent kinases, this protein functions as a regulator of the pre-mRNA splicing process, as well as in inducing apoptosis by modulating the expression of apoptotic and antiapoptotic proteins. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":1385711,"end":1399328,"strand":-1,"description":"cyclin L2 [Source:HGNC Symbol;Acc:HGNC:20570]"}, {"versioned_ensembl_gene_id":"ENSG00000244134.1","gene_symbol":"RPS12P20","gene_name":"ribosomal protein S12 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36187]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271549","summary":null,"start":72708186,"end":72708565,"strand":1,"description":"ribosomal protein S12 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36187]"}, {"versioned_ensembl_gene_id":"ENSG00000111581.9","gene_symbol":"NUP107","gene_name":"nucleoporin 107 [Source:HGNC Symbol;Acc:HGNC:29914]","synonyms":"NUP84","biotype":"protein_coding","ncbi_id":"57122","summary":"This gene encodes a member of the nucleoporin family. The protein is localized to the nuclear rim and is an essential component of the nuclear pore complex (NPC). All molecules entering or leaving the nucleus either diffuse through or are actively transported by the NPC. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":68686734,"end":68745809,"strand":1,"description":"nucleoporin 107 [Source:HGNC Symbol;Acc:HGNC:29914]"}, {"versioned_ensembl_gene_id":"ENSG00000213153.3","gene_symbol":"AP001979.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133864877,"end":133865627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167925.15","gene_symbol":"GHDC","gene_name":"GH3 domain containing [Source:HGNC Symbol;Acc:HGNC:24438]","synonyms":"LGP1","biotype":"protein_coding","ncbi_id":"84514","summary":null,"start":42188799,"end":42194532,"strand":-1,"description":"GH3 domain containing [Source:HGNC Symbol;Acc:HGNC:24438]"}, {"versioned_ensembl_gene_id":"ENSG00000274727.1","gene_symbol":"AL137028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64327418,"end":64327972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269793.6","gene_symbol":"ZIM2-AS1","gene_name":"ZIM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51304]","synonyms":"ZIM2as","biotype":"antisense_RNA","ncbi_id":"101929059","summary":null,"start":56765344,"end":56799646,"strand":1,"description":"ZIM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51304]"}, {"versioned_ensembl_gene_id":"ENSG00000268067.2","gene_symbol":"OR5AH1P","gene_name":"olfactory receptor family 5 subfamily AH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14714]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79336","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56690686,"end":56761215,"strand":1,"description":"olfactory receptor family 5 subfamily AH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14714]"}, {"versioned_ensembl_gene_id":"ENSG00000250484.2","gene_symbol":"AC108075.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124062462,"end":124062990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258435.1","gene_symbol":"AC048337.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121391962,"end":121399859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234365.6","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32877562,"end":32879971,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000254189.1","gene_symbol":"AC090095.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83099976,"end":83100846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254321.1","gene_symbol":"AC016813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38700626,"end":38704855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260878.1","gene_symbol":"AC104072.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":46243548,"end":46244215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234239.1","gene_symbol":"CFL1P8","gene_name":"cofilin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873812","summary":null,"start":99582706,"end":99583180,"strand":1,"description":"cofilin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39960]"}, {"versioned_ensembl_gene_id":"ENSG00000272328.1","gene_symbol":"AC007128.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8303741,"end":8341343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265254.1","gene_symbol":"AC015917.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28405240,"end":28406796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234354.3","gene_symbol":"RPS26P47","gene_name":"ribosomal protein S26 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400156","summary":null,"start":100539901,"end":100540248,"strand":-1,"description":"ribosomal protein S26 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36368]"}, {"versioned_ensembl_gene_id":"ENSG00000235615.2","gene_symbol":"AJ239322.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131964731,"end":131979873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256695.1","gene_symbol":"AC003982.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120389546,"end":120395994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273428.3","gene_symbol":"AC004832.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30435544,"end":30436247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125304.8","gene_symbol":"TM9SF2","gene_name":"transmembrane 9 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11865]","synonyms":"P76","biotype":"protein_coding","ncbi_id":"9375","summary":"This gene encodes a member of the transmembrane 9 superfamily. The encoded 76 kDa protein localizes to early endosomes in human cells. The encoded protein possesses a conserved and highly hydrophobic C-terminal domain which contains nine transmembrane domains. The protein may play a role in small molecule transport or act as an ion channel. A pseudogene associated with this gene is located on the X chromosome. [provided by RefSeq, Oct 2012]","start":99501417,"end":99564006,"strand":1,"description":"transmembrane 9 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11865]"}, {"versioned_ensembl_gene_id":"ENSG00000113615.12","gene_symbol":"SEC24A","gene_name":"SEC24 homolog A, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10703]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10802","summary":"The protein encoded by this gene belongs to a family of proteins that are homologous to yeast Sec24. This protein is a component of coat protein II (COPII)-coated vesicles that mediate protein transport from the endoplasmic reticulum. COPII acts in the cytoplasm to promote the transport of secretory, plasma membrane, and vacuolar proteins from the endoplasmic reticulum to the golgi complex. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":134648789,"end":134727823,"strand":1,"description":"SEC24 homolog A, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10703]"}, {"versioned_ensembl_gene_id":"ENSG00000270269.1","gene_symbol":"IMMP1LP1","gene_name":"inner mitochondrial membrane peptidase subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51131]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729101","summary":null,"start":63632233,"end":63632720,"strand":1,"description":"inner mitochondrial membrane peptidase subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51131]"}, {"versioned_ensembl_gene_id":"ENSG00000171988.18","gene_symbol":"JMJD1C","gene_name":"jumonji domain containing 1C [Source:HGNC Symbol;Acc:HGNC:12313]","synonyms":"KIAA1380,KDM3C,FLJ14374,DKFZp761F0118,TRIP8","biotype":"protein_coding","ncbi_id":"221037","summary":"The protein encoded by this gene interacts with thyroid hormone receptors and contains a jumonji domain. It is a candidate histone demethylase and is thought to be a coactivator for key transcription factors. It plays a role in the DNA-damage response pathway by demethylating the mediator of DNA damage checkpoint 1 (MDC1) protein, and is required for the survival of acute myeloid leukemia. Mutations in this gene are associated with Rett syndrome and intellectual disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":63167221,"end":63521850,"strand":-1,"description":"jumonji domain containing 1C [Source:HGNC Symbol;Acc:HGNC:12313]"}, {"versioned_ensembl_gene_id":"ENSG00000241899.1","gene_symbol":"TPT1P3","gene_name":"tumor protein, translationally-controlled 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49295]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421439","summary":null,"start":141709016,"end":141709832,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49295]"}, {"versioned_ensembl_gene_id":"ENSG00000282645.1","gene_symbol":"AC093627.19","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73293,"end":98004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082175.14","gene_symbol":"PGR","gene_name":"progesterone receptor [Source:HGNC Symbol;Acc:HGNC:8910]","synonyms":"PR,NR3C3","biotype":"protein_coding","ncbi_id":"5241","summary":"This gene encodes a member of the steroid receptor superfamily. The encoded protein mediates the physiological effects of progesterone, which plays a central role in reproductive events associated with the establishment and maintenance of pregnancy. This gene uses two distinct promotors and translation start sites in the first exon to produce several transcript variants, both protein coding and non-protein coding. Two of the isoforms (A and B) are identical except for an additional 165 amino acids found in the N-terminus of isoform B and mediate their own response genes and physiologic effects with little overlap. [provided by RefSeq, Sep 2015]","start":101029624,"end":101130524,"strand":-1,"description":"progesterone receptor [Source:HGNC Symbol;Acc:HGNC:8910]"}, {"versioned_ensembl_gene_id":"ENSG00000260660.3","gene_symbol":"AC113208.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":75226401,"end":75234014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170035.15","gene_symbol":"UBE2E3","gene_name":"ubiquitin conjugating enzyme E2 E3 [Source:HGNC Symbol;Acc:HGNC:12479]","synonyms":"UbcH9","biotype":"protein_coding","ncbi_id":"10477","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein shares 100% sequence identity with the mouse and rat counterparts, which indicates that this enzyme is highly conserved in eukaryotes. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2013]","start":180967248,"end":181076585,"strand":1,"description":"ubiquitin conjugating enzyme E2 E3 [Source:HGNC Symbol;Acc:HGNC:12479]"}, {"versioned_ensembl_gene_id":"ENSG00000227125.1","gene_symbol":"AP002856.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131204999,"end":131215163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224440.1","gene_symbol":"CXorf51A","gene_name":"chromosome X open reading frame 51A [Source:HGNC Symbol;Acc:HGNC:30533]","synonyms":"CXorf51","biotype":"protein_coding","ncbi_id":"100129239","summary":null,"start":146814106,"end":146814726,"strand":-1,"description":"chromosome X open reading frame 51A [Source:HGNC Symbol;Acc:HGNC:30533]"}, {"versioned_ensembl_gene_id":"ENSG00000175130.6","gene_symbol":"MARCKSL1","gene_name":"MARCKS like 1 [Source:HGNC Symbol;Acc:HGNC:7142]","synonyms":"MLP1,MLP,MacMARCKS,F52","biotype":"protein_coding","ncbi_id":"65108","summary":"This gene encodes a member of the myristoylated alanine-rich C-kinase substrate (MARCKS) family. Members of this family play a role in cytoskeletal regulation, protein kinase C signaling and calmodulin signaling. The encoded protein affects the formation of adherens junction. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are located on the long arm of chromosomes 6 and 10. [provided by RefSeq, Jun 2012]","start":32333832,"end":32336379,"strand":-1,"description":"MARCKS like 1 [Source:HGNC Symbol;Acc:HGNC:7142]"}, {"versioned_ensembl_gene_id":"ENSG00000227244.2","gene_symbol":"LINC00845","gene_name":"long intergenic non-protein coding RNA 845 [Source:HGNC Symbol;Acc:HGNC:45033]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507058","summary":null,"start":61016275,"end":61026420,"strand":1,"description":"long intergenic non-protein coding RNA 845 [Source:HGNC Symbol;Acc:HGNC:45033]"}, {"versioned_ensembl_gene_id":"ENSG00000237612.1","gene_symbol":"AP002856.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131234538,"end":131251816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228125.2","gene_symbol":"AKIRIN1P2","gene_name":"akirin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50797]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480306","summary":null,"start":68132868,"end":68133437,"strand":1,"description":"akirin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50797]"}, {"versioned_ensembl_gene_id":"ENSG00000146352.12","gene_symbol":"CLVS2","gene_name":"clavesin 2 [Source:HGNC Symbol;Acc:HGNC:23046]","synonyms":"RLBP1L2,C6orf213,C6orf212,bA160A10.4","biotype":"protein_coding","ncbi_id":"134829","summary":"This gene encodes a protein that belongs to the SEC14/CRAL-TRIO family of proteins. A similar protein in rat is thought to function in the endosomal pathway between early endosomes and mature lysosomes. [provided by RefSeq, Aug 2013]","start":122995971,"end":123072927,"strand":1,"description":"clavesin 2 [Source:HGNC Symbol;Acc:HGNC:23046]"}, {"versioned_ensembl_gene_id":"ENSG00000164597.13","gene_symbol":"COG5","gene_name":"component of oligomeric golgi complex 5 [Source:HGNC Symbol;Acc:HGNC:14857]","synonyms":"GTC90,GOLTC1","biotype":"protein_coding","ncbi_id":"10466","summary":"The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011]","start":107201555,"end":107564514,"strand":-1,"description":"component of oligomeric golgi complex 5 [Source:HGNC Symbol;Acc:HGNC:14857]"}, {"versioned_ensembl_gene_id":"ENSG00000168702.17","gene_symbol":"LRP1B","gene_name":"LDL receptor related protein 1B [Source:HGNC Symbol;Acc:HGNC:6693]","synonyms":"LRPDIT,LRP-DIT","biotype":"protein_coding","ncbi_id":"53353","summary":"This gene encodes a member of the low density lipoprotein (LDL) receptor family. These receptors play a wide variety of roles in normal cell function and development due to their interactions with multiple ligands. Disruption of this gene has been reported in several types of cancer. [provided by RefSeq, Jun 2016]","start":140231423,"end":142131701,"strand":-1,"description":"LDL receptor related protein 1B [Source:HGNC Symbol;Acc:HGNC:6693]"}, {"versioned_ensembl_gene_id":"ENSG00000225660.1","gene_symbol":"Z99497.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146955075,"end":146955209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079482.12","gene_symbol":"OPHN1","gene_name":"oligophrenin 1 [Source:HGNC Symbol;Acc:HGNC:8148]","synonyms":"OPN1,MRX60,ARHGAP41","biotype":"protein_coding","ncbi_id":"4983","summary":"This gene encodes a Rho-GTPase-activating protein that promotes GTP hydrolysis of Rho subfamily members. Rho proteins are important mediators of intracellular signal transduction, which affects cell migration and cell morphogenesis. Mutations in this gene are responsible for OPHN1-related X-linked cognitive disability with cerebellar hypoplasia and distinctive facial dysmorhphism. [provided by RefSeq, Jul 2008]","start":68042344,"end":68433913,"strand":-1,"description":"oligophrenin 1 [Source:HGNC Symbol;Acc:HGNC:8148]"}, {"versioned_ensembl_gene_id":"ENSG00000271660.1","gene_symbol":"Z99497.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146964176,"end":146964485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250488.1","gene_symbol":"LINC02233","gene_name":"long intergenic non-protein coding RNA 2233 [Source:HGNC Symbol;Acc:HGNC:53104]","synonyms":"RP11-6C14.1","biotype":"lincRNA","ncbi_id":"109729132","summary":null,"start":159666503,"end":159777784,"strand":-1,"description":"long intergenic non-protein coding RNA 2233 [Source:HGNC Symbol;Acc:HGNC:53104]"}, {"versioned_ensembl_gene_id":"ENSG00000242135.2","gene_symbol":"RPL17P2","gene_name":"ribosomal protein L17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652974","summary":null,"start":60212462,"end":60212912,"strand":-1,"description":"ribosomal protein L17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23540]"}, {"versioned_ensembl_gene_id":"ENSG00000108960.7","gene_symbol":"MMD","gene_name":"monocyte to macrophage differentiation associated [Source:HGNC Symbol;Acc:HGNC:7153]","synonyms":"PAQR11,MMA","biotype":"protein_coding","ncbi_id":"23531","summary":"This protein is expressed by in vitro differentiated macrophages but not freshly isolated monocytes. Although sequence analysis identifies seven potential transmembrane domains, this protein has little homology to G-protein receptors and it has not been positively identified as a receptor. A suggested alternative function is that of an ion channel protein in maturing macrophages. [provided by RefSeq, Jul 2008]","start":55392613,"end":55421992,"strand":-1,"description":"monocyte to macrophage differentiation associated [Source:HGNC Symbol;Acc:HGNC:7153]"}, {"versioned_ensembl_gene_id":"ENSG00000282045.1","gene_symbol":"IGHV3-66","gene_name":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28412","summary":null,"start":106699696,"end":106700225,"strand":-1,"description":"immunoglobulin heavy variable 3-66 [Source:HGNC Symbol;Acc:HGNC:5619]"}, {"versioned_ensembl_gene_id":"ENSG00000260041.5","gene_symbol":"AC007495.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56109537,"end":56137000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250997.1","gene_symbol":"AC093853.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160521829,"end":160522311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227492.1","gene_symbol":"AL138921.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100229667,"end":100234000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223619.1","gene_symbol":"MTCO1P17","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52019]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075222","summary":null,"start":202614214,"end":202614704,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52019]"}, {"versioned_ensembl_gene_id":"ENSG00000225145.1","gene_symbol":"HLA-S","gene_name":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]","synonyms":"HLA-17","biotype":"unprocessed_pseudogene","ncbi_id":"267015","summary":null,"start":31372541,"end":31372755,"strand":-1,"description":"major histocompatibility complex, class I, S (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19395]"}, {"versioned_ensembl_gene_id":"ENSG00000282439.1","gene_symbol":"IGHV1-67","gene_name":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28463","summary":null,"start":106705284,"end":106705723,"strand":-1,"description":"immunoglobulin heavy variable 1-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5556]"}, {"versioned_ensembl_gene_id":"ENSG00000279523.1","gene_symbol":"AC040168.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56108980,"end":56109970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230224.1","gene_symbol":"PHBP9","gene_name":"prohibitin pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39288]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289414","summary":null,"start":100248271,"end":100249095,"strand":1,"description":"prohibitin pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39288]"}, {"versioned_ensembl_gene_id":"ENSG00000249425.1","gene_symbol":"LINC02477","gene_name":"long intergenic non-protein coding RNA 2477 [Source:HGNC Symbol;Acc:HGNC:53425]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377512","summary":null,"start":160539254,"end":160586817,"strand":1,"description":"long intergenic non-protein coding RNA 2477 [Source:HGNC Symbol;Acc:HGNC:53425]"}, {"versioned_ensembl_gene_id":"ENSG00000282117.1","gene_symbol":"SLC20A1P1","gene_name":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192127","summary":null,"start":106708076,"end":106709031,"strand":-1,"description":"solute carrier family 20 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20051]"}, {"versioned_ensembl_gene_id":"ENSG00000246379.6","gene_symbol":"AC007495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56092987,"end":56191094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235453.9","gene_symbol":"SMIM27","gene_name":"small integral membrane protein 27 [Source:HGNC Symbol;Acc:HGNC:31420]","synonyms":"TOPORS-AS1,C9orf133","biotype":"protein_coding","ncbi_id":"100129250","summary":null,"start":32551144,"end":32568621,"strand":1,"description":"small integral membrane protein 27 [Source:HGNC Symbol;Acc:HGNC:31420]"}, {"versioned_ensembl_gene_id":"ENSG00000233775.1","gene_symbol":"AL109945.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32349194,"end":32350663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233888.2","gene_symbol":"MTCO2P17","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52033]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075268","summary":null,"start":202614853,"end":202615529,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52033]"}, {"versioned_ensembl_gene_id":"ENSG00000284377.1","gene_symbol":"AL589669.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147181064,"end":147271894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183822.3","gene_symbol":"NCF4-AS1","gene_name":"NCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40393]","synonyms":"CTA-833B7.2","biotype":"antisense_RNA","ncbi_id":"107985578","summary":null,"start":36847372,"end":36870441,"strand":-1,"description":"NCF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40393]"}, {"versioned_ensembl_gene_id":"ENSG00000205693.3","gene_symbol":"MANSC4","gene_name":"MANSC domain containing 4 [Source:HGNC Symbol;Acc:HGNC:40023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287284","summary":null,"start":27762738,"end":27771276,"strand":-1,"description":"MANSC domain containing 4 [Source:HGNC Symbol;Acc:HGNC:40023]"}, {"versioned_ensembl_gene_id":"ENSG00000274579.1","gene_symbol":"AL096861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147476324,"end":147476446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279319.1","gene_symbol":"AC105074.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44986109,"end":44989203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282652.1","gene_symbol":"IGHVII-67-1","gene_name":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]","synonyms":"IGHV(II)-67-1","biotype":"IG_V_pseudogene","ncbi_id":"28358","summary":null,"start":106711198,"end":106711243,"strand":-1,"description":"immunoglobulin heavy variable (II)-67-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5689]"}, {"versioned_ensembl_gene_id":"ENSG00000242635.2","gene_symbol":"RPS14P7","gene_name":"ribosomal protein S14 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36961]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271065","summary":null,"start":160818422,"end":160818869,"strand":1,"description":"ribosomal protein S14 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36961]"}, {"versioned_ensembl_gene_id":"ENSG00000228855.1","gene_symbol":"AL009048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147591612,"end":147591909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282016.1","gene_symbol":"IGHVIII-67-2","gene_name":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]","synonyms":"IGHV(III)-67-2","biotype":"IG_V_pseudogene","ncbi_id":"28342","summary":null,"start":106711794,"end":106711881,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5705]"}, {"versioned_ensembl_gene_id":"ENSG00000282161.1","gene_symbol":"IGHVIII-67-3","gene_name":"immunoglobulin heavy variable (III)-67-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5706]","synonyms":"IGHV(III)-67-3","biotype":"IG_V_pseudogene","ncbi_id":"28341","summary":null,"start":106717338,"end":106717569,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5706]"}, {"versioned_ensembl_gene_id":"ENSG00000227505.1","gene_symbol":"AC016925.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147801005,"end":147801302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261013.1","gene_symbol":"AC079411.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56183726,"end":56186306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105327.17","gene_symbol":"BBC3","gene_name":"BCL2 binding component 3 [Source:HGNC Symbol;Acc:HGNC:17868]","synonyms":"PUMA,JFY1","biotype":"protein_coding","ncbi_id":"27113","summary":"This gene encodes a member of the BCL-2 family of proteins. This family member belongs to the BH3-only pro-apoptotic subclass. The protein cooperates with direct activator proteins to induce mitochondrial outer membrane permeabilization and apoptosis. It can bind to anti-apoptotic Bcl-2 family members to induce mitochondrial dysfunction and caspase activation. Because of its pro-apoptotic role, this gene is a potential drug target for cancer therapy and for tissue injury. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":47220822,"end":47232766,"strand":-1,"description":"BCL2 binding component 3 [Source:HGNC Symbol;Acc:HGNC:17868]"}, {"versioned_ensembl_gene_id":"ENSG00000271175.1","gene_symbol":"AC016925.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147812733,"end":147812974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184303.5","gene_symbol":"DRD5P1","gene_name":"dopamine receptor D5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3027]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1817","summary":null,"start":91684447,"end":91685884,"strand":-1,"description":"dopamine receptor D5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3027]"}, {"versioned_ensembl_gene_id":"ENSG00000187847.4","gene_symbol":"OR7E25P","gene_name":"olfactory receptor family 7 subfamily E member 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:8397]","synonyms":"OR19-C,CIT-B-440L2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26647","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9198354,"end":9210067,"strand":1,"description":"olfactory receptor family 7 subfamily E member 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:8397]"}, {"versioned_ensembl_gene_id":"ENSG00000227083.1","gene_symbol":"L29074.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147900178,"end":147901459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268066.5","gene_symbol":"FMR1-AS1","gene_name":"FMR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39081]","synonyms":"FMR4,FMR1AS,FMR1-AS,ASFMR1","biotype":"processed_transcript","ncbi_id":"100126270","summary":null,"start":147909431,"end":147911817,"strand":-1,"description":"FMR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39081]"}, {"versioned_ensembl_gene_id":"ENSG00000115956.9","gene_symbol":"PLEK","gene_name":"pleckstrin [Source:HGNC Symbol;Acc:HGNC:9070]","synonyms":"P47","biotype":"protein_coding","ncbi_id":"5341","summary":null,"start":68365173,"end":68397453,"strand":1,"description":"pleckstrin [Source:HGNC Symbol;Acc:HGNC:9070]"}, {"versioned_ensembl_gene_id":"ENSG00000174667.4","gene_symbol":"OR7D4","gene_name":"olfactory receptor family 7 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:8380]","synonyms":"OR7D4P,OR19-B,hg105","biotype":"protein_coding","ncbi_id":"125958","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9210276,"end":9219589,"strand":-1,"description":"olfactory receptor family 7 subfamily D member 4 [Source:HGNC Symbol;Acc:HGNC:8380]"}, {"versioned_ensembl_gene_id":"ENSG00000165194.15","gene_symbol":"PCDH19","gene_name":"protocadherin 19 [Source:HGNC Symbol;Acc:HGNC:14270]","synonyms":"EIEE9,EFMR,KIAA1313","biotype":"protein_coding","ncbi_id":"57526","summary":"The protein encoded by this gene is a member of the delta-2 protocadherin subclass of the cadherin superfamily. The encoded protein is thought to be a calcium-dependent cell-adhesion protein that is primarily expressed in the brain. Mutations in this gene on human chromosome X are associated with sporadic infantile epileptic encephalopathy and to a female-restricted form of epilepsy (EFMR; also known as PCDH19RE). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":100291644,"end":100410273,"strand":-1,"description":"protocadherin 19 [Source:HGNC Symbol;Acc:HGNC:14270]"}, {"versioned_ensembl_gene_id":"ENSG00000231698.2","gene_symbol":"AP002856.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131253422,"end":131350917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176485.11","gene_symbol":"PLA2G16","gene_name":"phospholipase A2 group XVI [Source:HGNC Symbol;Acc:HGNC:17825]","synonyms":"MGC118754.,HREV107-3,HREV107,HRASLS3,H-REV107-1,AdPLA","biotype":"protein_coding","ncbi_id":"11145","summary":null,"start":63573195,"end":63616883,"strand":-1,"description":"phospholipase A2 group XVI [Source:HGNC Symbol;Acc:HGNC:17825]"}, {"versioned_ensembl_gene_id":"ENSG00000261873.2","gene_symbol":"AC006269.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55448433,"end":55511444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230572.5","gene_symbol":"AC027612.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91686102,"end":91714745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166710.17","gene_symbol":"B2M","gene_name":"beta-2-microglobulin [Source:HGNC Symbol;Acc:HGNC:914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"567","summary":"This gene encodes a serum protein found in association with the major histocompatibility complex (MHC) class I heavy chain on the surface of nearly all nucleated cells. The protein has a predominantly beta-pleated sheet structure that can form amyloid fibrils in some pathological conditions. The encoded antimicrobial protein displays antibacterial activity in amniotic fluid. A mutation in this gene has been shown to result in hypercatabolic hypoproteinemia.[provided by RefSeq, Aug 2014]","start":44711477,"end":44718877,"strand":1,"description":"beta-2-microglobulin [Source:HGNC Symbol;Acc:HGNC:914]"}, {"versioned_ensembl_gene_id":"ENSG00000237233.2","gene_symbol":"TMEM26-AS1","gene_name":"TMEM26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51209]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928781","summary":null,"start":61452639,"end":61481956,"strand":1,"description":"TMEM26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51209]"}, {"versioned_ensembl_gene_id":"ENSG00000236319.2","gene_symbol":"AC105021.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":55526964,"end":55561577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196932.11","gene_symbol":"TMEM26","gene_name":"transmembrane protein 26 [Source:HGNC Symbol;Acc:HGNC:28550]","synonyms":"MGC35010,Em:AC068892.1","biotype":"protein_coding","ncbi_id":"219623","summary":"This gene encodes a protein containing multiple transmembrane helices. It is a selective surface protein marker of brite/beige adipocytes, which may coexist with classical brown adipocytes in brown adipose tissue. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":61406643,"end":61453450,"strand":-1,"description":"transmembrane protein 26 [Source:HGNC Symbol;Acc:HGNC:28550]"}, {"versioned_ensembl_gene_id":"ENSG00000237098.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29887810,"end":29888941,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000262135.1","gene_symbol":"GARSP1","gene_name":"glycyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50480]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419764","summary":null,"start":55550931,"end":55551649,"strand":-1,"description":"glycyl-tRNA synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50480]"}, {"versioned_ensembl_gene_id":"ENSG00000234364.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29849214,"end":29849342,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000184574.9","gene_symbol":"LPAR5","gene_name":"lysophosphatidic acid receptor 5 [Source:HGNC Symbol;Acc:HGNC:13307]","synonyms":"LPA5,KPG_010,GPR93,GPR92","biotype":"protein_coding","ncbi_id":"57121","summary":"This gene encodes a member of the rhodopsin class of G protein-coupled transmembrane receptors. This protein transmits extracellular signals from lysophosphatidic acid to cells through heterotrimeric G proteins and mediates numerous cellular processes. Many G protein receptors serve as targets for pharmaceutical drugs. Transcript variants of this gene have been described.[provided by RefSeq, Dec 2008]","start":6618835,"end":6636447,"strand":-1,"description":"lysophosphatidic acid receptor 5 [Source:HGNC Symbol;Acc:HGNC:13307]"}, {"versioned_ensembl_gene_id":"ENSG00000164853.8","gene_symbol":"UNCX","gene_name":"UNC homeobox [Source:HGNC Symbol;Acc:HGNC:33194]","synonyms":"Uncx4.1","biotype":"protein_coding","ncbi_id":"340260","summary":"This gene encodes a homeobox transcription factor that is involved in somitogenesis and neurogenesis and is required for the maintenance and differentiation of specific elements of the axial skeleton. This gene also plays a role in controlling the development of connections of hypothalamic neurons to pituitary elements, allowing central neurons to reach the peripheral blood circulation and deliver hormones that control peripheral functions. The expression of this gene is associated with an increased frequency of acute myeloid leukemia. [provided by RefSeq, Jul 2017]","start":1232907,"end":1237318,"strand":1,"description":"UNC homeobox [Source:HGNC Symbol;Acc:HGNC:33194]"}, {"versioned_ensembl_gene_id":"ENSG00000236265.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29897781,"end":29898147,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000228921.1","gene_symbol":"CR759762.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30021043,"end":30021554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253269.1","gene_symbol":"AC008680.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169772966,"end":169779365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203520.3","gene_symbol":"AP000753.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63616308,"end":63621671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166292.11","gene_symbol":"TMEM100","gene_name":"transmembrane protein 100 [Source:HGNC Symbol;Acc:HGNC:25607]","synonyms":"FLJ37856,FLJ10970","biotype":"protein_coding","ncbi_id":"55273","summary":null,"start":55719627,"end":55732121,"strand":-1,"description":"transmembrane protein 100 [Source:HGNC Symbol;Acc:HGNC:25607]"}, {"versioned_ensembl_gene_id":"ENSG00000233134.1","gene_symbol":"MTND3P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52077]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075279","summary":null,"start":202617284,"end":202617627,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52077]"}, {"versioned_ensembl_gene_id":"ENSG00000263327.6","gene_symbol":"TAPT1-AS1","gene_name":"TAPT1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26832]","synonyms":"FLJ39653","biotype":"antisense_RNA","ncbi_id":"202020","summary":null,"start":16226685,"end":16320140,"strand":1,"description":"TAPT1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:26832]"}, {"versioned_ensembl_gene_id":"ENSG00000237216.8","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29823845,"end":29828003,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000172530.20","gene_symbol":"BANP","gene_name":"BTG3 associated nuclear protein [Source:HGNC Symbol;Acc:HGNC:13450]","synonyms":"SMARBP1,SMAR1,FLJ20538,FLJ10177,DKFZp761H172,BEND1","biotype":"protein_coding","ncbi_id":"54971","summary":"This gene encodes a protein that binds to matrix attachment regions. The protein forms a complex with p53 and negatively regulates p53 transcription, and functions as a tumor suppressor and cell cycle regulator. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":87949244,"end":88077318,"strand":1,"description":"BTG3 associated nuclear protein [Source:HGNC Symbol;Acc:HGNC:13450]"}, {"versioned_ensembl_gene_id":"ENSG00000134516.15","gene_symbol":"DOCK2","gene_name":"dedicator of cytokinesis 2 [Source:HGNC Symbol;Acc:HGNC:2988]","synonyms":"KIAA0209","biotype":"protein_coding","ncbi_id":"1794","summary":"The protein encoded by this gene belongs to the CDM protein family. It is specifically expressed in hematopoietic cells and is predominantly expressed in peripheral blood leukocytes. The protein is involved in remodeling of the actin cytoskeleton required for lymphocyte migration in response to chemokine signaling. It activates members of the Rho family of GTPases, for example RAC1 and RAC2, by acting as a guanine nucleotide exchange factor (GEF) to exchange bound GDP for free GTP. Mutations in this gene result in immunodeficiency 40 (IMD40), a combined form of immunodeficiency that affects T cell number and function, also with variable defects in B cell and NK cell function. [provided by RefSeq, May 2018]","start":169637247,"end":170083382,"strand":1,"description":"dedicator of cytokinesis 2 [Source:HGNC Symbol;Acc:HGNC:2988]"}, {"versioned_ensembl_gene_id":"ENSG00000257989.1","gene_symbol":"AC078864.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52092485,"end":52104297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257542.4","gene_symbol":"OR7E47P","gene_name":"olfactory receptor family 7 subfamily E member 47 pseudogene [Source:HGNC Symbol;Acc:HGNC:8421]","synonyms":"OR7E141,OR7E141","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26628","summary":null,"start":52079696,"end":52108261,"strand":1,"description":"olfactory receptor family 7 subfamily E member 47 pseudogene [Source:HGNC Symbol;Acc:HGNC:8421]"}, {"versioned_ensembl_gene_id":"ENSG00000272724.1","gene_symbol":"OR7E47P","gene_name":"olfactory receptor family 7 subfamily E member 47 pseudogene [Source:NCBI gene;Acc:26628]","synonyms":"OR7E141,OR7E141","biotype":"sense_intronic","ncbi_id":"26628","summary":null,"start":52084744,"end":52092285,"strand":1,"description":"olfactory receptor family 7 subfamily E member 47 pseudogene [Source:NCBI gene;Acc:26628]"}, {"versioned_ensembl_gene_id":"ENSG00000203395.2","gene_symbol":"AC015969.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68361214,"end":68365584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257663.1","gene_symbol":"AC025259.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52076841,"end":52082084,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111644.7","gene_symbol":"ACRBP","gene_name":"acrosin binding protein [Source:HGNC Symbol;Acc:HGNC:17195]","synonyms":"SP32,OY-TES-1,CT23","biotype":"protein_coding","ncbi_id":"84519","summary":"The protein encoded by this gene is similar to proacrosin binding protein sp32 precursor found in mouse, guinea pig, and pig. This protein is located in the sperm acrosome and is thought to function as a binding protein to proacrosin for packaging and condensation of the acrosin zymogen in the acrosomal matrix. This protein is a member of the cancer/testis family of antigens and it is found to be immunogenic. In normal tissues, this mRNA is expressed only in testis, whereas it is detected in a range of different tumor types such as bladder, breast, lung, liver, and colon. [provided by RefSeq, Jul 2008]","start":6638075,"end":6647460,"strand":-1,"description":"acrosin binding protein [Source:HGNC Symbol;Acc:HGNC:17195]"}, {"versioned_ensembl_gene_id":"ENSG00000123395.14","gene_symbol":"ATG101","gene_name":"autophagy related 101 [Source:HGNC Symbol;Acc:HGNC:25679]","synonyms":"FLJ11773,C12orf44","biotype":"protein_coding","ncbi_id":"60673","summary":null,"start":52069246,"end":52077494,"strand":1,"description":"autophagy related 101 [Source:HGNC Symbol;Acc:HGNC:25679]"}, {"versioned_ensembl_gene_id":"ENSG00000188314.3","gene_symbol":"OR7D1P","gene_name":"olfactory receptor family 7 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8377]","synonyms":"OR7D3P,OR7D3,OR19-A","biotype":"unprocessed_pseudogene","ncbi_id":"26656","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9235144,"end":9236076,"strand":1,"description":"olfactory receptor family 7 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8377]"}, {"versioned_ensembl_gene_id":"ENSG00000259509.2","gene_symbol":"AC073941.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46827526,"end":46827958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282257.1","gene_symbol":"AC118653.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71596338,"end":71597279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168843.13","gene_symbol":"FSTL5","gene_name":"follistatin like 5 [Source:HGNC Symbol;Acc:HGNC:21386]","synonyms":"KIAA1263,DKFZp566D234","biotype":"protein_coding","ncbi_id":"56884","summary":null,"start":161383897,"end":162164035,"strand":-1,"description":"follistatin like 5 [Source:HGNC Symbol;Acc:HGNC:21386]"}, {"versioned_ensembl_gene_id":"ENSG00000256747.1","gene_symbol":"AC009511.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27779821,"end":27781067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256512.1","gene_symbol":"AC009511.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27798641,"end":27800708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129933.20","gene_symbol":"MAU2","gene_name":"MAU2 sister chromatid cohesion factor [Source:HGNC Symbol;Acc:HGNC:29140]","synonyms":"SCC4,MGC75361,MAU2L,mau-2,KIAA0892","biotype":"protein_coding","ncbi_id":"23383","summary":null,"start":19320681,"end":19358755,"strand":1,"description":"MAU2 sister chromatid cohesion factor [Source:HGNC Symbol;Acc:HGNC:29140]"}, {"versioned_ensembl_gene_id":"ENSG00000237521.3","gene_symbol":"OR7E24","gene_name":"olfactory receptor family 7 subfamily E member 24 [Source:HGNC Symbol;Acc:HGNC:8396]","synonyms":"OR7E24Q,OR7E24P,OR19-8,HSHT2","biotype":"protein_coding","ncbi_id":"26648","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9247344,"end":9252625,"strand":1,"description":"olfactory receptor family 7 subfamily E member 24 [Source:HGNC Symbol;Acc:HGNC:8396]"}, {"versioned_ensembl_gene_id":"ENSG00000087448.9","gene_symbol":"KLHL42","gene_name":"kelch like family member 42 [Source:HGNC Symbol;Acc:HGNC:29252]","synonyms":"KIAA1340,Ctb9,KLHDC5","biotype":"protein_coding","ncbi_id":"57542","summary":null,"start":27780020,"end":27803040,"strand":1,"description":"kelch like family member 42 [Source:HGNC Symbol;Acc:HGNC:29252]"}, {"versioned_ensembl_gene_id":"ENSG00000275193.2","gene_symbol":"MYL6P5","gene_name":"myosin light chain 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"124685","summary":null,"start":71620978,"end":71621436,"strand":1,"description":"myosin light chain 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51646]"}, {"versioned_ensembl_gene_id":"ENSG00000284540.1","gene_symbol":"AC066615.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47133495,"end":47134122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000043143.20","gene_symbol":"JADE2","gene_name":"jade family PHD finger 2 [Source:HGNC Symbol;Acc:HGNC:22984]","synonyms":"PHF15,KIAA0239,JADE-2","biotype":"protein_coding","ncbi_id":"23338","summary":null,"start":134524312,"end":134583230,"strand":1,"description":"jade family PHD finger 2 [Source:HGNC Symbol;Acc:HGNC:22984]"}, {"versioned_ensembl_gene_id":"ENSG00000282185.1","gene_symbol":"PTPRN2","gene_name":"protein tyrosine phosphatase, receptor type N2 [Source:HGNC Symbol;Acc:HGNC:9677]","synonyms":"phogrin,KIAA0387,ICAAR,IA-2beta","biotype":"protein_coding","ncbi_id":"5799","summary":"This gene encodes a protein with sequence similarity to receptor-like protein tyrosine phosphatases. However, tyrosine phosphatase activity has not been experimentally validated for this protein. Studies of the rat ortholog suggest that the encoded protein may instead function as a phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4,5-diphosphate, and this function may be involved in the regulation of insulin secretion. This protein has been identified as an autoantigen in insulin-dependent diabetes mellitus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":158291152,"end":158424386,"strand":-1,"description":"protein tyrosine phosphatase, receptor type N2 [Source:HGNC Symbol;Acc:HGNC:9677]"}, {"versioned_ensembl_gene_id":"ENSG00000227627.2","gene_symbol":"AL080276.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152983331,"end":152990541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259321.1","gene_symbol":"AL136295.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24139445,"end":24140444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112029.9","gene_symbol":"FBXO5","gene_name":"F-box protein 5 [Source:HGNC Symbol;Acc:HGNC:13584]","synonyms":"FBX5,EMI1,Fbxo31","biotype":"protein_coding","ncbi_id":"26271","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. This protein is similar to xenopus early mitotic inhibitor-1 (Emi1), which is a mitotic regulator that interacts with Cdc20 and inhibits the anaphase promoting complex. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Dec 2008]","start":152970519,"end":152983579,"strand":-1,"description":"F-box protein 5 [Source:HGNC Symbol;Acc:HGNC:13584]"}, {"versioned_ensembl_gene_id":"ENSG00000238262.1","gene_symbol":"NTM-IT","gene_name":"NTM intronic transcript [Source:HGNC Symbol;Acc:HGNC:41437]","synonyms":"NTM-IT3","biotype":"sense_intronic","ncbi_id":"100874281","summary":null,"start":132284302,"end":132285081,"strand":1,"description":"NTM intronic transcript [Source:HGNC Symbol;Acc:HGNC:41437]"}, {"versioned_ensembl_gene_id":"ENSG00000100908.13","gene_symbol":"EMC9","gene_name":"ER membrane protein complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:20273]","synonyms":"FAM158A,CGI-112,C14orf122","biotype":"protein_coding","ncbi_id":"51016","summary":null,"start":24138959,"end":24141588,"strand":-1,"description":"ER membrane protein complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:20273]"}, {"versioned_ensembl_gene_id":"ENSG00000238117.1","gene_symbol":"AP000844.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131877680,"end":131897108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224795.1","gene_symbol":"NTM-AS1","gene_name":"NTM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32293]","synonyms":"FLJ45436,C11orf39","biotype":"lincRNA","ncbi_id":"101929637","summary":null,"start":131662131,"end":131663583,"strand":-1,"description":"NTM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32293]"}, {"versioned_ensembl_gene_id":"ENSG00000160221.16","gene_symbol":"C21orf33","gene_name":"chromosome 21 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:1273]","synonyms":"KNPI,KNPH,KNP-Ia,KNP-I,HES1,GT335,ES1,D21S2048E","biotype":"protein_coding","ncbi_id":"8209","summary":"This gene encodes a potential mitochondrial protein that is a member of the DJ-1/PfpI gene family. This protein is overexpressed in fetal Down syndrome brain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":44133605,"end":44145723,"strand":1,"description":"chromosome 21 open reading frame 33 [Source:HGNC Symbol;Acc:HGNC:1273]"}, {"versioned_ensembl_gene_id":"ENSG00000271624.1","gene_symbol":"AP004372.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131770795,"end":131771638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282808.1","gene_symbol":"IGHVIII-67-4","gene_name":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]","synonyms":"IGHV(III)-67-4","biotype":"IG_V_pseudogene","ncbi_id":"28340","summary":null,"start":106719783,"end":106720078,"strand":-1,"description":"immunoglobulin heavy variable (III)-67-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5707]"}, {"versioned_ensembl_gene_id":"ENSG00000136521.12","gene_symbol":"NDUFB5","gene_name":"NADH:ubiquinone oxidoreductase subunit B5 [Source:HGNC Symbol;Acc:HGNC:7700]","synonyms":"SGDH,MGC12314,CI-SGDH","biotype":"protein_coding","ncbi_id":"4711","summary":"The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":179604690,"end":179627647,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B5 [Source:HGNC Symbol;Acc:HGNC:7700]"}, {"versioned_ensembl_gene_id":"ENSG00000182667.14","gene_symbol":"NTM","gene_name":"neurotrimin [Source:HGNC Symbol;Acc:HGNC:17941]","synonyms":"IGLON2,HNT,NTRI","biotype":"protein_coding","ncbi_id":"50863","summary":"This gene encodes a member of the IgLON (LAMP, OBCAM, Ntm) family of immunoglobulin (Ig) domain-containing glycosylphosphatidylinositol (GPI)-anchored cell adhesion molecules. The encoded protein may promote neurite outgrowth and adhesion via a homophilic mechanism. This gene is closely linked to a related family member, opioid binding protein/cell adhesion molecule-like (OPCML), on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":131370478,"end":132336822,"strand":1,"description":"neurotrimin [Source:HGNC Symbol;Acc:HGNC:17941]"}, {"versioned_ensembl_gene_id":"ENSG00000016490.15","gene_symbol":"CLCA1","gene_name":"chloride channel accessory 1 [Source:HGNC Symbol;Acc:HGNC:2015]","synonyms":"CLCRG1,CaCC","biotype":"protein_coding","ncbi_id":"1179","summary":"This gene encodes a member of the calcium sensitive chloride conductance protein family. To date, all members of this gene family map to the same region on chromosome 1p31-p22 and share a high degree of homology in size, sequence, and predicted structure, but differ significantly in their tissue distributions. The encoded protein is expressed as a precursor protein that is processed into two cell-surface-associated subunits, although the site at which the precursor is cleaved has not been precisely determined. The encoded protein may be involved in mediating calcium-activated chloride conductance in the intestine. [provided by RefSeq, Jul 2008]","start":86468368,"end":86500289,"strand":1,"description":"chloride channel accessory 1 [Source:HGNC Symbol;Acc:HGNC:2015]"}, {"versioned_ensembl_gene_id":"ENSG00000254111.2","gene_symbol":"AC124067.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37560366,"end":37565377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254290.1","gene_symbol":"AC124067.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37597480,"end":37599858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225828.1","gene_symbol":"FAM229A","gene_name":"family with sequence similarity 229 member A [Source:HGNC Symbol;Acc:HGNC:44652]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100128071","summary":null,"start":32361270,"end":32364278,"strand":-1,"description":"family with sequence similarity 229 member A [Source:HGNC Symbol;Acc:HGNC:44652]"}, {"versioned_ensembl_gene_id":"ENSG00000254306.1","gene_symbol":"AC137579.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37600537,"end":37625873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233082.1","gene_symbol":"AC073094.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1267353,"end":1269267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253344.1","gene_symbol":"AC137579.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37626015,"end":37674387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275940.1","gene_symbol":"MRPL57P3","gene_name":"mitochondrial ribosomal protein L57 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29688]","synonyms":"MRP63P3","biotype":"processed_pseudogene","ncbi_id":"359730","summary":null,"start":47028855,"end":47029030,"strand":1,"description":"mitochondrial ribosomal protein L57 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29688]"}, {"versioned_ensembl_gene_id":"ENSG00000258537.5","gene_symbol":"FRMD6-AS2","gene_name":"FRMD6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43637]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874185","summary":null,"start":51454512,"end":51599952,"strand":-1,"description":"FRMD6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43637]"}, {"versioned_ensembl_gene_id":"ENSG00000183779.6","gene_symbol":"ZNF703","gene_name":"zinc finger protein 703 [Source:HGNC Symbol;Acc:HGNC:25883]","synonyms":"Zpo1,ZNF503L,ZEPPO1,NLZ1,FLJ14299","biotype":"protein_coding","ncbi_id":"80139","summary":null,"start":37695751,"end":37700021,"strand":1,"description":"zinc finger protein 703 [Source:HGNC Symbol;Acc:HGNC:25883]"}, {"versioned_ensembl_gene_id":"ENSG00000172403.10","gene_symbol":"SYNPO2","gene_name":"synaptopodin 2 [Source:HGNC Symbol;Acc:HGNC:17732]","synonyms":"MYOPODIN","biotype":"protein_coding","ncbi_id":"171024","summary":null,"start":118850688,"end":119061247,"strand":1,"description":"synaptopodin 2 [Source:HGNC Symbol;Acc:HGNC:17732]"}, {"versioned_ensembl_gene_id":"ENSG00000181555.20","gene_symbol":"SETD2","gene_name":"SET domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18420]","synonyms":"KMT3A,KIAA1732,HYPB,HIF-1,FLJ23184","biotype":"protein_coding","ncbi_id":"29072","summary":"Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein belonging to a class of huntingtin interacting proteins characterized by WW motifs. This protein is a histone methyltransferase that is specific for lysine-36 of histone H3, and methylation of this residue is associated with active chromatin. This protein also contains a novel transcriptional activation domain and has been found associated with hyperphosphorylated RNA polymerase II. [provided by RefSeq, Aug 2008]","start":47016429,"end":47163967,"strand":-1,"description":"SET domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18420]"}, {"versioned_ensembl_gene_id":"ENSG00000162526.6","gene_symbol":"TSSK3","gene_name":"testis specific serine kinase 3 [Source:HGNC Symbol;Acc:HGNC:15473]","synonyms":"STK22C,SPOGA3","biotype":"protein_coding","ncbi_id":"81629","summary":"This gene encodes a kinase expressed exclusively in the testis that is thought to play a role in either germ cell differentiation or mature sperm function. [provided by RefSeq, Jul 2008]","start":32351521,"end":32364312,"strand":1,"description":"testis specific serine kinase 3 [Source:HGNC Symbol;Acc:HGNC:15473]"}, {"versioned_ensembl_gene_id":"ENSG00000225558.1","gene_symbol":"UBE2D3P2","gene_name":"ubiquitin conjugating enzyme E2 D3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39010]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130139","summary":null,"start":37134658,"end":37135102,"strand":1,"description":"ubiquitin conjugating enzyme E2 D3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39010]"}, {"versioned_ensembl_gene_id":"ENSG00000139926.15","gene_symbol":"FRMD6","gene_name":"FERM domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19839]","synonyms":"willin,MGC17921,EX1,C14orf31","biotype":"protein_coding","ncbi_id":"122786","summary":null,"start":51489100,"end":51730727,"strand":1,"description":"FERM domain containing 6 [Source:HGNC Symbol;Acc:HGNC:19839]"}, {"versioned_ensembl_gene_id":"ENSG00000271993.1","gene_symbol":"AC126118.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37182107,"end":37182734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126088.13","gene_symbol":"UROD","gene_name":"uroporphyrinogen decarboxylase [Source:HGNC Symbol;Acc:HGNC:12591]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7389","summary":"This gene encodes an enzyme in the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.[provided by RefSeq, Aug 2010]","start":45012147,"end":45015575,"strand":1,"description":"uroporphyrinogen decarboxylase [Source:HGNC Symbol;Acc:HGNC:12591]"}, {"versioned_ensembl_gene_id":"ENSG00000277975.1","gene_symbol":"CSTP2","gene_name":"cystatin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2487]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"1481","summary":null,"start":23772785,"end":23776169,"strand":-1,"description":"cystatin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2487]"}, {"versioned_ensembl_gene_id":"ENSG00000253181.1","gene_symbol":"AC138356.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37717579,"end":37733756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230908.1","gene_symbol":"AL591074.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23798141,"end":23805663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093167.17","gene_symbol":"LRRFIP2","gene_name":"LRR binding FLII interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:6703]","synonyms":"HUFI-2","biotype":"protein_coding","ncbi_id":"9209","summary":"The protein encoded by this gene, along with MYD88, binds to the cytosolic tail of toll-like receptor 4 (TLR4), which results in activation of nuclear factor kappa B signaling. The ubiquitin-like protein FAT10 prevents the interaction of the encoded protein and TLR4, thereby inactivating the nuclear factor kappa B signaling pathway. In addition, this protein can downregulate the NLRP3 inflammasome by recruiting the caspase-1 inhibitor Flightless-I to the inflammasome complex. [provided by RefSeq, Jan 2017]","start":37052656,"end":37183689,"strand":-1,"description":"LRR binding FLII interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:6703]"}, {"versioned_ensembl_gene_id":"ENSG00000282055.1","gene_symbol":"IGHV1-68","gene_name":"immunoglobulin heavy variable 1-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5557]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28462","summary":null,"start":106728533,"end":106728827,"strand":-1,"description":"immunoglobulin heavy variable 1-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5557]"}, {"versioned_ensembl_gene_id":"ENSG00000282350.1","gene_symbol":"IGHV1-69","gene_name":"immunoglobulin heavy variable 1-69 [Source:HGNC Symbol;Acc:HGNC:5558]","synonyms":"IGHV1-E","biotype":"IG_V_gene","ncbi_id":"28461","summary":null,"start":106739363,"end":106739862,"strand":-1,"description":"immunoglobulin heavy variable 1-69 [Source:HGNC Symbol;Acc:HGNC:5558]"}, {"versioned_ensembl_gene_id":"ENSG00000229173.1","gene_symbol":"AC108059.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128139792,"end":128140516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136731.12","gene_symbol":"UGGT1","gene_name":"UDP-glucose glycoprotein glucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15663]","synonyms":"UGCGL1,HUGT1","biotype":"protein_coding","ncbi_id":"56886","summary":"UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009]","start":128091200,"end":128195677,"strand":1,"description":"UDP-glucose glycoprotein glucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15663]"}, {"versioned_ensembl_gene_id":"ENSG00000234809.8","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30766531,"end":30769904,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000099725.14","gene_symbol":"PRKY","gene_name":"protein kinase, Y-linked, pseudogene [Source:HGNC Symbol;Acc:HGNC:9444]","synonyms":"PRKYP,PRKXP3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5616","summary":"This gene is similar to the protein kinase, X-linked gene in the pseudoautosomal region of the X chromosome. The gene is classified as a transcribed pseudogene because it has lost a coding exon that results in all transcripts being candidates for nonsense-mediated decay (NMD) and unlikely to express a protein. Abnormal recombination between this gene and a related gene on chromosome X is a frequent cause of XX males and XY females. [provided by RefSeq, Jul 2010]","start":7273972,"end":7381548,"strand":1,"description":"protein kinase, Y-linked, pseudogene [Source:HGNC Symbol;Acc:HGNC:9444]"}, {"versioned_ensembl_gene_id":"ENSG00000168283.13","gene_symbol":"BMI1","gene_name":"BMI1 proto-oncogene, polycomb ring finger [Source:HGNC Symbol;Acc:HGNC:1066]","synonyms":"RNF51,PCGF4","biotype":"protein_coding","ncbi_id":"648","summary":"This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015]","start":22321211,"end":22331484,"strand":1,"description":"BMI1 proto-oncogene, polycomb ring finger [Source:HGNC Symbol;Acc:HGNC:1066]"}, {"versioned_ensembl_gene_id":"ENSG00000175348.10","gene_symbol":"TMEM9B","gene_name":"TMEM9 domain family member B [Source:HGNC Symbol;Acc:HGNC:1168]","synonyms":"C11orf15","biotype":"protein_coding","ncbi_id":"56674","summary":null,"start":8947294,"end":8965011,"strand":-1,"description":"TMEM9 domain family member B [Source:HGNC Symbol;Acc:HGNC:1168]"}, {"versioned_ensembl_gene_id":"ENSG00000135097.6","gene_symbol":"MSI1","gene_name":"musashi RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7330]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4440","summary":"This gene encodes a protein containing two conserved tandem RNA recognition motifs. Similar proteins in other species function as RNA-binding proteins and play central roles in posttranscriptional gene regulation. Expression of this gene has been correlated with the grade of the malignancy and proliferative activity in gliomas and melanomas. A pseudogene for this gene is located on chromosome 11q13. [provided by RefSeq, Jul 2008]","start":120341330,"end":120369180,"strand":-1,"description":"musashi RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7330]"}, {"versioned_ensembl_gene_id":"ENSG00000276166.1","gene_symbol":"AC092118.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57759358,"end":57760024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233051.9","gene_symbol":"MICA","gene_name":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]","synonyms":"PERB11.1","biotype":"protein_coding","ncbi_id":"100507436","summary":"This gene encodes the highly polymorphic major histocompatability complex class I chain-related protein A. The protein product is expressed on the cell surface, although unlike canonical class I molecules it does not seem to associate with beta-2-microglobulin. It is a ligand for the NKG2-D type II integral membrane protein receptor. The protein functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells. Variations in this gene have been associated with susceptibility to psoriasis 1 and psoriatic arthritis, and the shedding of MICA-related antibodies and ligands is involved in the progression from monoclonal gammopathy of undetermined significance to multiple myeloma. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31390270,"end":31406729,"strand":1,"description":"MHC class I polypeptide-related sequence A [Source:HGNC Symbol;Acc:HGNC:7090]"}, {"versioned_ensembl_gene_id":"ENSG00000228341.1","gene_symbol":"AC002381.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107450083,"end":107450362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231314.7","gene_symbol":"LTB","gene_name":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]","synonyms":"TNFC,p33,TNFSF3","biotype":"protein_coding","ncbi_id":"4050","summary":"Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":31647541,"end":31649508,"strand":-1,"description":"lymphotoxin beta [Source:HGNC Symbol;Acc:HGNC:6711]"}, {"versioned_ensembl_gene_id":"ENSG00000092010.14","gene_symbol":"PSME1","gene_name":"proteasome activator subunit 1 [Source:HGNC Symbol;Acc:HGNC:9568]","synonyms":"PA28alpha,IFI5111","biotype":"protein_coding","ncbi_id":"5720","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the alpha subunit of the 11S regulator, one of the two 11S subunits that is induced by gamma-interferon. Three alpha and three beta subunits combine to form a heterohexameric ring. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":24136158,"end":24138967,"strand":1,"description":"proteasome activator subunit 1 [Source:HGNC Symbol;Acc:HGNC:9568]"}, {"versioned_ensembl_gene_id":"ENSG00000105856.13","gene_symbol":"HBP1","gene_name":"HMG-box transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:23200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26959","summary":null,"start":107168961,"end":107202529,"strand":1,"description":"HMG-box transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:23200]"}, {"versioned_ensembl_gene_id":"ENSG00000170647.3","gene_symbol":"TMEM133","gene_name":"transmembrane protein 133 [Source:HGNC Symbol;Acc:HGNC:24033]","synonyms":"AD031","biotype":"protein_coding","ncbi_id":"83935","summary":"There is evidence that this intronless gene is transcribed but the protein is predicted. The gene function is unknown. [provided by RefSeq, Jul 2008]","start":100991989,"end":100993941,"strand":1,"description":"transmembrane protein 133 [Source:HGNC Symbol;Acc:HGNC:24033]"}, {"versioned_ensembl_gene_id":"ENSG00000109182.11","gene_symbol":"CWH43","gene_name":"cell wall biogenesis 43 C-terminal homolog [Source:HGNC Symbol;Acc:HGNC:26133]","synonyms":"FLJ21511,CWH43-C","biotype":"protein_coding","ncbi_id":"80157","summary":null,"start":48986247,"end":49062081,"strand":1,"description":"cell wall biogenesis 43 C-terminal homolog [Source:HGNC Symbol;Acc:HGNC:26133]"}, {"versioned_ensembl_gene_id":"ENSG00000232160.6","gene_symbol":"RAP2C-AS1","gene_name":"RAP2C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40957]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928578","summary":null,"start":132217147,"end":132432862,"strand":1,"description":"RAP2C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40957]"}, {"versioned_ensembl_gene_id":"ENSG00000249419.1","gene_symbol":"AC023136.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162022733,"end":162047567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105705.15","gene_symbol":"SUGP1","gene_name":"SURP and G-patch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18643]","synonyms":"DKFZp434E2216,SF4,RBP,F23858","biotype":"protein_coding","ncbi_id":"57794","summary":"SF4 is a member of the SURP family of splicing factors.[supplied by OMIM, Sep 2003]","start":19276018,"end":19320844,"strand":-1,"description":"SURP and G-patch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18643]"}, {"versioned_ensembl_gene_id":"ENSG00000249568.1","gene_symbol":"AC104793.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161378953,"end":161388417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147475.14","gene_symbol":"ERLIN2","gene_name":"ER lipid raft associated 2 [Source:HGNC Symbol;Acc:HGNC:1356]","synonyms":"SPG18,SPFH2,NET32,Erlin-2,C8orf2","biotype":"protein_coding","ncbi_id":"11160","summary":"This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":37736599,"end":37759101,"strand":1,"description":"ER lipid raft associated 2 [Source:HGNC Symbol;Acc:HGNC:1356]"}, {"versioned_ensembl_gene_id":"ENSG00000235433.1","gene_symbol":"MTATP6P17","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52062]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075274","summary":null,"start":202615769,"end":202616440,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52062]"}, {"versioned_ensembl_gene_id":"ENSG00000145569.5","gene_symbol":"FAM105A","gene_name":"family with sequence similarity 105 member A [Source:HGNC Symbol;Acc:HGNC:25629]","synonyms":"NET20,FLJ11127","biotype":"protein_coding","ncbi_id":"54491","summary":null,"start":14581775,"end":14615007,"strand":1,"description":"family with sequence similarity 105 member A [Source:HGNC Symbol;Acc:HGNC:25629]"}, {"versioned_ensembl_gene_id":"ENSG00000105321.12","gene_symbol":"CCDC9","gene_name":"coiled-coil domain containing 9 [Source:HGNC Symbol;Acc:HGNC:24560]","synonyms":"DKFZP586M1019","biotype":"protein_coding","ncbi_id":"26093","summary":null,"start":47255980,"end":47271953,"strand":1,"description":"coiled-coil domain containing 9 [Source:HGNC Symbol;Acc:HGNC:24560]"}, {"versioned_ensembl_gene_id":"ENSG00000123728.9","gene_symbol":"RAP2C","gene_name":"RAP2C, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:21165]","synonyms":"DKFZp313B211","biotype":"protein_coding","ncbi_id":"57826","summary":"The protein encoded by this gene is a member of the Ras-related protein subfamily of the Ras GTPase superfamily. Members of this family are small GTPases that act as molecular switches to regulate cellular proliferation, differentiation, and apoptosis. This protein has been reported to activate in vitro transcriptional activity of the serum response element. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":132203024,"end":132219480,"strand":-1,"description":"RAP2C, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:21165]"}, {"versioned_ensembl_gene_id":"ENSG00000237542.1","gene_symbol":"MTCO3P17","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52047]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075271","summary":null,"start":202616700,"end":202617212,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52047]"}, {"versioned_ensembl_gene_id":"ENSG00000260430.1","gene_symbol":"AC099518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19086856,"end":19098110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117691.9","gene_symbol":"NENF","gene_name":"neudesin neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:30384]","synonyms":"SPUF,SCIRP10,CIR2","biotype":"protein_coding","ncbi_id":"29937","summary":"This gene encodes a neurotrophic factor that may play a role in neuron differentiation and development. A pseudogene of this gene is found on chromosome 12. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":212432887,"end":212446379,"strand":1,"description":"neudesin neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:30384]"}, {"versioned_ensembl_gene_id":"ENSG00000280563.1","gene_symbol":"NXN","gene_name":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]","synonyms":"NRX,FLJ12614","biotype":"protein_coding","ncbi_id":"64359","summary":"This gene encodes a member of the thioredoxin superfamily, a group of small, multifunctional redox-active proteins. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. The encoded protein acts a redox-dependent regulator of the Wnt signaling pathway and is involved in cell growth and differentiation. [provided by RefSeq, Sep 2015]","start":978299,"end":979770,"strand":-1,"description":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]"}, {"versioned_ensembl_gene_id":"ENSG00000228613.1","gene_symbol":"AC141930.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1546665,"end":1620113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237549.1","gene_symbol":"AC092570.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101509530,"end":101510222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232556.1","gene_symbol":"AC092570.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101520834,"end":101521976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282482.1","gene_symbol":"AC245369.6","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106748255,"end":106748774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231482.2","gene_symbol":"AC141930.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1572554,"end":1580311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000021574.11","gene_symbol":"SPAST","gene_name":"spastin [Source:HGNC Symbol;Acc:HGNC:11233]","synonyms":"SPG4,KIAA1083,FSP2,ADPSP","biotype":"protein_coding","ncbi_id":"6683","summary":"This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The use of alternative translational initiation sites in this gene results in a single transcript variant that can produce isoforms that differ in the length of their N-terminus and which thereby differ in the efficiency of their export from the nucleus to the cytoplasm. In addition, alternative splicing results in multiple transcript variants that encode isoforms that differ in other protein regions as well. One isoform of this gene has been shown to be a microtubule-severing enzyme that regulates microtubule abundance, mobility, and plus-end distribution. Mutations in this gene cause the most frequent form of autosomal dominant spastic paraplegia 4. [provided by RefSeq, May 2018]","start":32063611,"end":32157637,"strand":1,"description":"spastin [Source:HGNC Symbol;Acc:HGNC:11233]"}, {"versioned_ensembl_gene_id":"ENSG00000254860.5","gene_symbol":"TMEM9B-AS1","gene_name":"TMEM9B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19230]","synonyms":"C11orf18","biotype":"antisense_RNA","ncbi_id":"493900","summary":null,"start":8964675,"end":8977527,"strand":1,"description":"TMEM9B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19230]"}, {"versioned_ensembl_gene_id":"ENSG00000283766.1","gene_symbol":"AC141930.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1552445,"end":1554701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104537.16","gene_symbol":"ANXA13","gene_name":"annexin A13 [Source:HGNC Symbol;Acc:HGNC:536]","synonyms":"ANX13","biotype":"protein_coding","ncbi_id":"312","summary":"This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. The specific function of this gene has not yet been determined; however, it is associated with the plasma membrane of undifferentiated, proliferating endothelial cells and differentiated villus enterocytes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":123680794,"end":123737407,"strand":-1,"description":"annexin A13 [Source:HGNC Symbol;Acc:HGNC:536]"}, {"versioned_ensembl_gene_id":"ENSG00000232649.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29899020,"end":29899882,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000225120.1","gene_symbol":"CT009517.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878546,"end":29879514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258446.1","gene_symbol":"AL133153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91419449,"end":91419751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258798.1","gene_symbol":"AL133153.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91418266,"end":91421176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281951.1","gene_symbol":"AC093627.11","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19790,"end":37822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270930.1","gene_symbol":"GRAMD4P8","gene_name":"GRAM domain containing 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49143]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631247","summary":null,"start":131646704,"end":131648372,"strand":-1,"description":"GRAM domain containing 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49143]"}, {"versioned_ensembl_gene_id":"ENSG00000240268.6","gene_symbol":"MOXD2P","gene_name":"monooxygenase, DBH-like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33605]","synonyms":"MOXD2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100289017","summary":null,"start":142240740,"end":142247067,"strand":-1,"description":"monooxygenase, DBH-like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:33605]"}, {"versioned_ensembl_gene_id":"ENSG00000224559.2","gene_symbol":"LINC01087","gene_name":"long intergenic non-protein coding RNA 1087 [Source:HGNC Symbol;Acc:HGNC:49144]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927994","summary":null,"start":131637025,"end":131649615,"strand":1,"description":"long intergenic non-protein coding RNA 1087 [Source:HGNC Symbol;Acc:HGNC:49144]"}, {"versioned_ensembl_gene_id":"ENSG00000224700.2","gene_symbol":"AP000844.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131981096,"end":131984661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236082.2","gene_symbol":"AP003025.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131546662,"end":131573600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258563.2","gene_symbol":"PSMA3P","gene_name":"proteasome subunit alpha 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:20029]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326617","summary":null,"start":60179382,"end":60180016,"strand":1,"description":"proteasome subunit alpha 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:20029]"}, {"versioned_ensembl_gene_id":"ENSG00000237654.5","gene_symbol":"AP003025.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":131502759,"end":131540867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249234.1","gene_symbol":"AC108063.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16178939,"end":16183120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180926.6","gene_symbol":"OR7E18P","gene_name":"olfactory receptor family 7 subfamily E member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:8389]","synonyms":"TPCR26,OR7E98P,OR7E61,OR19-14","biotype":"unprocessed_pseudogene","ncbi_id":"390885","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9261015,"end":9261716,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:8389]"}, {"versioned_ensembl_gene_id":"ENSG00000089558.8","gene_symbol":"KCNH4","gene_name":"potassium voltage-gated channel subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:6253]","synonyms":"Kv12.3,elk1","biotype":"protein_coding","ncbi_id":"23415","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. The gene is brain-specific, and located in the neocortex and the striatum. It may be involved in cellular excitability of restricted neurons in the central nervous system. [provided by RefSeq, Jul 2008]","start":42156891,"end":42181278,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 4 [Source:HGNC Symbol;Acc:HGNC:6253]"}, {"versioned_ensembl_gene_id":"ENSG00000259768.5","gene_symbol":"AC004943.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72665170,"end":72791624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197927.12","gene_symbol":"C2orf27A","gene_name":"chromosome 2 open reading frame 27A [Source:HGNC Symbol;Acc:HGNC:25077]","synonyms":"C2orf27","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"29798","summary":null,"start":131722375,"end":131767404,"strand":1,"description":"chromosome 2 open reading frame 27A [Source:HGNC Symbol;Acc:HGNC:25077]"}, {"versioned_ensembl_gene_id":"ENSG00000205220.11","gene_symbol":"PSMB10","gene_name":"proteasome subunit beta 10 [Source:HGNC Symbol;Acc:HGNC:9538]","synonyms":"MGC1665,MECL1,LMP10,beta2i","biotype":"protein_coding","ncbi_id":"5699","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. Proteolytic processing is required to generate a mature subunit. Expression of this gene is induced by gamma interferon, and this gene product replaces catalytic subunit 2 (proteasome beta 7 subunit) in the immunoproteasome. [provided by RefSeq, Jul 2008]","start":67934502,"end":67937087,"strand":-1,"description":"proteasome subunit beta 10 [Source:HGNC Symbol;Acc:HGNC:9538]"}, {"versioned_ensembl_gene_id":"ENSG00000225980.4","gene_symbol":"OR7E19P","gene_name":"olfactory receptor family 7 subfamily E member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:8390]","synonyms":"OR7E65,OR19-7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26651","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9265440,"end":9268819,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:8390]"}, {"versioned_ensembl_gene_id":"ENSG00000170369.3","gene_symbol":"CST2","gene_name":"cystatin SA [Source:HGNC Symbol;Acc:HGNC:2474]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1470","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a secreted thiol protease inhibitor found at high levels in saliva, tears and seminal plasma. [provided by RefSeq, Jul 2008]","start":23823769,"end":23826731,"strand":-1,"description":"cystatin SA [Source:HGNC Symbol;Acc:HGNC:2474]"}, {"versioned_ensembl_gene_id":"ENSG00000273355.1","gene_symbol":"AP000894.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":813274,"end":813756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226480.1","gene_symbol":"OR7H1P","gene_name":"olfactory receptor family 7 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8468]","synonyms":"OR7H1","biotype":"unprocessed_pseudogene","ncbi_id":"390886","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9278448,"end":9279369,"strand":-1,"description":"olfactory receptor family 7 subfamily H member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8468]"}, {"versioned_ensembl_gene_id":"ENSG00000242358.1","gene_symbol":"RPS21P4","gene_name":"ribosomal protein S21 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128912","summary":null,"start":16256308,"end":16256555,"strand":-1,"description":"ribosomal protein S21 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35922]"}, {"versioned_ensembl_gene_id":"ENSG00000248851.1","gene_symbol":"AC006427.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16307456,"end":16308167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169762.16","gene_symbol":"TAPT1","gene_name":"transmembrane anterior posterior transformation 1 [Source:HGNC Symbol;Acc:HGNC:26887]","synonyms":"FLJ90013","biotype":"protein_coding","ncbi_id":"202018","summary":"This gene encodes a highly conserved protein that localizes to the centrosome and/or ciliary basal body. Mutations in this gene disrupt Golgi morphology and trafficking and normal primary cilium formation and these mutations are congenitally manifested by severe undermineralization of the intra-uterine skeleton. A mutation in the mouse ortholog of this gene results in homeotic, posterior-to-anterior transformations of the axial skeleton which are similar to the phenotype of mouse homeobox C8 gene mutants. In mouse, this gene is thought to function downstream of homeobox C8 to transduce extracellular patterning information during axial skeleton development. [provided by RefSeq, Jan 2017]","start":16160505,"end":16227410,"strand":-1,"description":"transmembrane anterior posterior transformation 1 [Source:HGNC Symbol;Acc:HGNC:26887]"}, {"versioned_ensembl_gene_id":"ENSG00000183346.6","gene_symbol":"C10orf107","gene_name":"chromosome 10 open reading frame 107 [Source:HGNC Symbol;Acc:HGNC:28678]","synonyms":"bA63A2.1,MGC44593,Em:AC022398.2","biotype":"protein_coding","ncbi_id":"219621","summary":null,"start":61662961,"end":61766766,"strand":1,"description":"chromosome 10 open reading frame 107 [Source:HGNC Symbol;Acc:HGNC:28678]"}, {"versioned_ensembl_gene_id":"ENSG00000282333.1","gene_symbol":"AC093627.15","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39354,"end":39799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284688.1","gene_symbol":"AL121936.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26477872,"end":26478533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213222.3","gene_symbol":"AC093724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131723253,"end":131724279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100614.17","gene_symbol":"PPM1A","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1A [Source:HGNC Symbol;Acc:HGNC:9275]","synonyms":"MGC9201,PP2Calpha,PP2CA","biotype":"protein_coding","ncbi_id":"5494","summary":"The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. This phosphatase dephosphorylates, and negatively regulates the activities of, MAP kinases and MAP kinase kinases. It has been shown to inhibit the activation of p38 and JNK kinase cascades induced by environmental stresses. This phosphatase can also dephosphorylate cyclin-dependent kinases, and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to activate the expression of the tumor suppressor gene TP53/p53, which leads to G2/M cell cycle arrest and apoptosis. Three alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":60245752,"end":60299087,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1A [Source:HGNC Symbol;Acc:HGNC:9275]"}, {"versioned_ensembl_gene_id":"ENSG00000278665.1","gene_symbol":"AC020765.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28599241,"end":28601881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229241.1","gene_symbol":"PNPT1P1","gene_name":"polyribonucleotide nucleotidyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44468]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288506","summary":null,"start":3981981,"end":3984295,"strand":-1,"description":"polyribonucleotide nucleotidyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44468]"}, {"versioned_ensembl_gene_id":"ENSG00000279512.1","gene_symbol":"AC011755.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":133117004,"end":133119052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170367.4","gene_symbol":"CST5","gene_name":"cystatin D [Source:HGNC Symbol;Acc:HGNC:2477]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1473","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a protein found in saliva and tears. The encoded protein may play a protective role against proteinases present in the oral cavity. [provided by RefSeq, Jul 2008]","start":23875935,"end":23879750,"strand":-1,"description":"cystatin D [Source:HGNC Symbol;Acc:HGNC:2477]"}, {"versioned_ensembl_gene_id":"ENSG00000278725.1","gene_symbol":"AC020765.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28602340,"end":28604519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203635.2","gene_symbol":"AC144450.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1620510,"end":1625419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238244.3","gene_symbol":"GABARAPL3","gene_name":"GABA type A receptor associated protein like 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4069]","synonyms":"ATG8D,ATG8D","biotype":"processed_pseudogene","ncbi_id":"23766","summary":null,"start":90348844,"end":90349197,"strand":-1,"description":"GABA type A receptor associated protein like 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4069]"}, {"versioned_ensembl_gene_id":"ENSG00000141179.13","gene_symbol":"PCTP","gene_name":"phosphatidylcholine transfer protein [Source:HGNC Symbol;Acc:HGNC:8752]","synonyms":"STARD2","biotype":"protein_coding","ncbi_id":"58488","summary":null,"start":55750979,"end":55842830,"strand":1,"description":"phosphatidylcholine transfer protein [Source:HGNC Symbol;Acc:HGNC:8752]"}, {"versioned_ensembl_gene_id":"ENSG00000204231.10","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"H-2RIIBP,RCoR-1,NR2B2","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33193588,"end":33200688,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000016602.9","gene_symbol":"CLCA4","gene_name":"chloride channel accessory 4 [Source:HGNC Symbol;Acc:HGNC:2018]","synonyms":"CaCC2","biotype":"protein_coding","ncbi_id":"22802","summary":"The protein encoded by this gene belongs to the calcium sensitive chloride conductance protein family. To date, all members of this gene family map to the same site on chromosome 1p31-p22 and share high degrees of homology in size, sequence and predicted structure, but differ significantly in their tissue distributions. Alternative splicing results in multiple transcript variants, only one of which is thought to be protein coding. [provided by RefSeq, Dec 2008]","start":86547078,"end":86580754,"strand":1,"description":"chloride channel accessory 4 [Source:HGNC Symbol;Acc:HGNC:2018]"}, {"versioned_ensembl_gene_id":"ENSG00000131171.12","gene_symbol":"SH3BGRL","gene_name":"SH3 domain binding glutamate rich protein like [Source:HGNC Symbol;Acc:HGNC:10823]","synonyms":"MGC117402","biotype":"protein_coding","ncbi_id":"6451","summary":null,"start":81201943,"end":81298547,"strand":1,"description":"SH3 domain binding glutamate rich protein like [Source:HGNC Symbol;Acc:HGNC:10823]"}, {"versioned_ensembl_gene_id":"ENSG00000196502.11","gene_symbol":"SULT1A1","gene_name":"sulfotransferase family 1A member 1 [Source:HGNC Symbol;Acc:HGNC:11453]","synonyms":"STP1,STP,P-PST","biotype":"protein_coding","ncbi_id":"6817","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes one of two phenol sulfotransferases with thermostable enzyme activity. Multiple alternatively spliced variants that encode two isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":28605196,"end":28623625,"strand":-1,"description":"sulfotransferase family 1A member 1 [Source:HGNC Symbol;Acc:HGNC:11453]"}, {"versioned_ensembl_gene_id":"ENSG00000196391.10","gene_symbol":"ZNF774","gene_name":"zinc finger protein 774 [Source:HGNC Symbol;Acc:HGNC:33108]","synonyms":"MGC75360","biotype":"protein_coding","ncbi_id":"342132","summary":null,"start":90352245,"end":90369146,"strand":1,"description":"zinc finger protein 774 [Source:HGNC Symbol;Acc:HGNC:33108]"}, {"versioned_ensembl_gene_id":"ENSG00000283559.1","gene_symbol":"AC139491.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":176143450,"end":176156989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139734.17","gene_symbol":"DIAPH3","gene_name":"diaphanous related formin 3 [Source:HGNC Symbol;Acc:HGNC:15480]","synonyms":"NSDAN,FLJ34705,DRF3,AUNA1,AN","biotype":"protein_coding","ncbi_id":"81624","summary":"This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":59665583,"end":60163987,"strand":-1,"description":"diaphanous related formin 3 [Source:HGNC Symbol;Acc:HGNC:15480]"}, {"versioned_ensembl_gene_id":"ENSG00000261884.2","gene_symbol":"AC040162.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":67929614,"end":67936017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283235.1","gene_symbol":"AC139493.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":176173345,"end":176199295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248791.1","gene_symbol":"AC010627.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14620020,"end":14621313,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250526.1","gene_symbol":"CCT6P2","gene_name":"chaperonin containing TCP1 subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391739","summary":null,"start":14639426,"end":14641018,"strand":-1,"description":"chaperonin containing TCP1 subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35150]"}, {"versioned_ensembl_gene_id":"ENSG00000141433.12","gene_symbol":"ADCYAP1","gene_name":"adenylate cyclase activating polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:241]","synonyms":"PACAP","biotype":"protein_coding","ncbi_id":"116","summary":"This gene encodes a secreted proprotein that is further processed into multiple mature peptides. These peptides stimulate adenylate cyclase and increase cyclic adenosine monophosphate (cAMP) levels, resulting in the transcriptional activation of target genes. The products of this gene are key mediators of neuroendocrine stress responses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]","start":904943,"end":912172,"strand":1,"description":"adenylate cyclase activating polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:241]"}, {"versioned_ensembl_gene_id":"ENSG00000248223.1","gene_symbol":"AC026785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17353910,"end":17354899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136450.12","gene_symbol":"SRSF1","gene_name":"serine and arginine rich splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:10780]","synonyms":"SRp30a,SFRS1,SF2p33,SF2,MGC5228,ASF","biotype":"protein_coding","ncbi_id":"6426","summary":"This gene encodes a member of the arginine/serine-rich splicing factor protein family. The encoded protein can either activate or repress splicing, depending on its phosphorylation state and its interaction partners. Multiple transcript variants have been found for this gene. There is a pseudogene of this gene on chromosome 13. [provided by RefSeq, Jun 2014]","start":58003360,"end":58007346,"strand":-1,"description":"serine and arginine rich splicing factor 1 [Source:HGNC Symbol;Acc:HGNC:10780]"}, {"versioned_ensembl_gene_id":"ENSG00000256285.1","gene_symbol":"OSBPL9P5","gene_name":"oxysterol binding protein like 9 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48735]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480232","summary":null,"start":66563524,"end":66563694,"strand":1,"description":"oxysterol binding protein like 9 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48735]"}, {"versioned_ensembl_gene_id":"ENSG00000271387.1","gene_symbol":"AL445228.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184385753,"end":184386704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242325.1","gene_symbol":"RPS12P31","gene_name":"ribosomal protein S12 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35578]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130192","summary":null,"start":32636078,"end":32636475,"strand":1,"description":"ribosomal protein S12 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35578]"}, {"versioned_ensembl_gene_id":"ENSG00000278305.1","gene_symbol":"AL161616.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31419989,"end":31437999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255530.1","gene_symbol":"AF235103.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145005561,"end":145005906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148737.16","gene_symbol":"TCF7L2","gene_name":"transcription factor 7 like 2 [Source:HGNC Symbol;Acc:HGNC:11641]","synonyms":"TCF4,TCF-4","biotype":"protein_coding","ncbi_id":"6934","summary":"This gene encodes a high mobility group (HMG) box-containing transcription factor that plays a key role in the Wnt signaling pathway. The protein has been implicated in blood glucose homeostasis. Genetic variants of this gene are associated with increased risk of type 2 diabetes. Several transcript variants encoding multiple different isoforms have been found for this gene.[provided by RefSeq, Oct 2010]","start":112950250,"end":113167678,"strand":1,"description":"transcription factor 7 like 2 [Source:HGNC Symbol;Acc:HGNC:11641]"}, {"versioned_ensembl_gene_id":"ENSG00000232474.1","gene_symbol":"NCKAP5-IT1","gene_name":"NCKAP5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41497]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874346","summary":null,"start":133431666,"end":133433897,"strand":-1,"description":"NCKAP5 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41497]"}, {"versioned_ensembl_gene_id":"ENSG00000276591.1","gene_symbol":"GXYLT1P5","gene_name":"glucoside xylosyltransferase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50424]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100131760","summary":null,"start":42974855,"end":42978320,"strand":1,"description":"glucoside xylosyltransferase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50424]"}, {"versioned_ensembl_gene_id":"ENSG00000125505.16","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173412,"end":54189882,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000236316.2","gene_symbol":"OR7E109P","gene_name":"olfactory receptor family 7 subfamily E member 109 pseudogene [Source:HGNC Symbol;Acc:HGNC:15118]","synonyms":"OST721","biotype":"unprocessed_pseudogene","ncbi_id":"401540","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":90742526,"end":90743380,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 109 pseudogene [Source:HGNC Symbol;Acc:HGNC:15118]"}, {"versioned_ensembl_gene_id":"ENSG00000105419.17","gene_symbol":"MEIS3","gene_name":"Meis homeobox 3 [Source:HGNC Symbol;Acc:HGNC:29537]","synonyms":"MRG2,DKFZp547H236","biotype":"protein_coding","ncbi_id":"56917","summary":"This gene encodes a homeobox protein and probable transcriptional regulator. The orthologous protein in mouse controls expression of 3-phosphoinositide dependent protein kinase 1, which promotes survival of pancreatic beta-cells. [provided by RefSeq, Sep 2016]","start":47403124,"end":47419523,"strand":-1,"description":"Meis homeobox 3 [Source:HGNC Symbol;Acc:HGNC:29537]"}, {"versioned_ensembl_gene_id":"ENSG00000223620.3","gene_symbol":"RBM48P1","gene_name":"RNA binding motif protein 48 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44054]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"132817","summary":null,"start":126563509,"end":126564776,"strand":1,"description":"RNA binding motif protein 48 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44054]"}, {"versioned_ensembl_gene_id":"ENSG00000260337.3","gene_symbol":"AC091544.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":92592574,"end":92596462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169598.15","gene_symbol":"DFFB","gene_name":"DNA fragmentation factor subunit beta [Source:HGNC Symbol;Acc:HGNC:2773]","synonyms":"CPAN,CAD,DFF40,DFF-40","biotype":"protein_coding","ncbi_id":"1677","summary":"Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of some of these variants has not been determined. [provided by RefSeq, Sep 2013]","start":3857267,"end":3885429,"strand":1,"description":"DNA fragmentation factor subunit beta [Source:HGNC Symbol;Acc:HGNC:2773]"}, {"versioned_ensembl_gene_id":"ENSG00000123106.10","gene_symbol":"CCDC91","gene_name":"coiled-coil domain containing 91 [Source:HGNC Symbol;Acc:HGNC:24855]","synonyms":"p56,FLJ11088,DKFZp779L1558","biotype":"protein_coding","ncbi_id":"55297","summary":null,"start":28133249,"end":28581511,"strand":1,"description":"coiled-coil domain containing 91 [Source:HGNC Symbol;Acc:HGNC:24855]"}, {"versioned_ensembl_gene_id":"ENSG00000254255.1","gene_symbol":"AC060788.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131712512,"end":131712980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113763.10","gene_symbol":"UNC5A","gene_name":"unc-5 netrin receptor A [Source:HGNC Symbol;Acc:HGNC:12567]","synonyms":"UNC5H1,KIAA1976","biotype":"protein_coding","ncbi_id":"90249","summary":"UNC5A belongs to a family of netrin-1 (MIM 601614) receptors thought to mediate the chemorepulsive effect of netrin-1 on specific axons. For more information on UNC5 proteins, see UNC5C (MIM 603610).[supplied by OMIM, Apr 2004]","start":176810477,"end":176880895,"strand":1,"description":"unc-5 netrin receptor A [Source:HGNC Symbol;Acc:HGNC:12567]"}, {"versioned_ensembl_gene_id":"ENSG00000269516.6","gene_symbol":"CYP4F23P","gene_name":"cytochrome P450 family 4 subfamily F member 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:39944]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100422238","summary":null,"start":15564074,"end":15584709,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:39944]"}, {"versioned_ensembl_gene_id":"ENSG00000230211.1","gene_symbol":"AL662847.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31515566,"end":31516145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277044.3","gene_symbol":"OPRL1","gene_name":"opioid related nociceptin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8155]","synonyms":"NOCIR,KOR-3,ORL1,OOR,NOPr","biotype":"protein_coding","ncbi_id":"4987","summary":"The protein encoded by this gene is a member of the 7 transmembrane-spanning G protein-coupled receptor family, and functions as a receptor for the endogenous, opioid-related neuropeptide, nociceptin/orphanin FQ. This receptor-ligand system modulates a variety of biological functions and neurobehavior, including stress responses and anxiety behavior, learning and memory, locomotor activity, and inflammatory and immune responses. A promoter region between this gene and the 5'-adjacent RGS19 (regulator of G-protein signaling 19) gene on the opposite strand functions bi-directionally as a core-promoter for both genes, suggesting co-operative transcriptional regulation of these two functionally related genes. Alternatively spliced transcript variants have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]","start":64097802,"end":64100643,"strand":1,"description":"opioid related nociceptin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8155]"}, {"versioned_ensembl_gene_id":"ENSG00000224870.6","gene_symbol":"AL391244.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1399522,"end":1402046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253898.1","gene_symbol":"LINC01419","gene_name":"long intergenic non-protein coding RNA 1419 [Source:HGNC Symbol;Acc:HGNC:50712]","synonyms":"TCONS_00014497","biotype":"lincRNA","ncbi_id":"103352670","summary":null,"start":83403758,"end":83408900,"strand":1,"description":"long intergenic non-protein coding RNA 1419 [Source:HGNC Symbol;Acc:HGNC:50712]"}, {"versioned_ensembl_gene_id":"ENSG00000248309.7","gene_symbol":"MEF2C-AS1","gene_name":"MEF2C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48908]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929423","summary":null,"start":88883328,"end":89466398,"strand":1,"description":"MEF2C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48908]"}, {"versioned_ensembl_gene_id":"ENSG00000076067.12","gene_symbol":"RBMS2","gene_name":"RNA binding motif single stranded interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:9909]","synonyms":"SCR3","biotype":"protein_coding","ncbi_id":"5939","summary":"The protein encoded by this gene is a member of a small family of proteins which bind single stranded DNA/RNA. These proteins are characterized by the presence of two sets of ribonucleoprotein consensus sequence (RNP-CS) that contain conserved motifs, RNP1 and RNP2, originally described in RNA binding proteins, and required for DNA binding. The RBMS proteins have been implicated in such diverse functions as DNA replication, gene transcription, cell cycle progression and apoptosis. This protein was isolated by phenotypic complementation of cdc2 and cdc13 mutants of yeast and is thought to suppress cdc2 and cdc13 mutants through the induction of translation of cdc2. [provided by RefSeq, Jul 2008]","start":56521929,"end":56596196,"strand":1,"description":"RNA binding motif single stranded interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:9909]"}, {"versioned_ensembl_gene_id":"ENSG00000261193.1","gene_symbol":"AC134312.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88079161,"end":88087383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234910.2","gene_symbol":"IL6RP1","gene_name":"interleukin 6 receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6020]","synonyms":"IL6RL1","biotype":"processed_pseudogene","ncbi_id":"157916","summary":null,"start":90081297,"end":90082569,"strand":-1,"description":"interleukin 6 receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6020]"}, {"versioned_ensembl_gene_id":"ENSG00000237372.2","gene_symbol":"UNQ6494","gene_name":"uncharacterized LOC100129066 [Source:NCBI gene;Acc:100129066]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129066","summary":null,"start":89639814,"end":89719759,"strand":1,"description":"uncharacterized LOC100129066 [Source:NCBI gene;Acc:100129066]"}, {"versioned_ensembl_gene_id":"ENSG00000227398.3","gene_symbol":"KIF9-AS1","gene_name":"KIF9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26822]","synonyms":"FLJ39534","biotype":"antisense_RNA","ncbi_id":"285352","summary":null,"start":47164497,"end":47246601,"strand":1,"description":"KIF9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26822]"}, {"versioned_ensembl_gene_id":"ENSG00000126214.21","gene_symbol":"KLC1","gene_name":"kinesin light chain 1 [Source:HGNC Symbol;Acc:HGNC:6387]","synonyms":"KNS2A,KNS2,KLC,hKLC1S,hKLC1R,hKLC1P,hKLC1N,hKLC1J,hKLC1G,hKLC1B","biotype":"protein_coding","ncbi_id":"3831","summary":"Conventional kinesin is a tetrameric molecule composed of two heavy chains and two light chains, and transports various cargos along microtubules toward their plus ends. The heavy chains provide the motor activity, while the light chains bind to various cargos. This gene encodes a member of the kinesin light chain family. It associates with kinesin heavy chain through an N-terminal domain, and six tetratricopeptide repeat (TPR) motifs are thought to be involved in binding of cargos such as vesicles, mitochondria, and the Golgi complex. Thus, kinesin light chains function as adapter molecules and not motors per se. Although previously named \"kinesin 2\", this gene is not a member of the kinesin-2 / kinesin heavy chain subfamily of kinesin motor proteins. Extensive alternative splicing produces isoforms with different C-termini that are proposed to bind to different cargos; however, the full-length nature and/or biological validity of most of these variants have not been determined. [provided by RefSeq, Jul 2008]","start":103561896,"end":103714249,"strand":1,"description":"kinesin light chain 1 [Source:HGNC Symbol;Acc:HGNC:6387]"}, {"versioned_ensembl_gene_id":"ENSG00000219500.1","gene_symbol":"AL391417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86432244,"end":86432669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269958.1","gene_symbol":"AL049840.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":103696353,"end":103697163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114648.11","gene_symbol":"KLHL18","gene_name":"kelch like family member 18 [Source:HGNC Symbol;Acc:HGNC:29120]","synonyms":"KIAA0795,FLJ13703","biotype":"protein_coding","ncbi_id":"23276","summary":null,"start":47282917,"end":47346816,"strand":1,"description":"kelch like family member 18 [Source:HGNC Symbol;Acc:HGNC:29120]"}, {"versioned_ensembl_gene_id":"ENSG00000232691.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":30079474,"end":30140140,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000126756.11","gene_symbol":"UXT","gene_name":"ubiquitously expressed prefoldin like chaperone [Source:HGNC Symbol;Acc:HGNC:12641]","synonyms":"STAP1,ART-27","biotype":"protein_coding","ncbi_id":"8409","summary":"The protein encoded by this gene functions as a cofactor that modulates androgen receptor-dependent transcription, and also plays a critical role in tumor necrosis factor-induced apoptosis. Expression of this gene may play a role in tumorigenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":47651798,"end":47659161,"strand":-1,"description":"ubiquitously expressed prefoldin like chaperone [Source:HGNC Symbol;Acc:HGNC:12641]"}, {"versioned_ensembl_gene_id":"ENSG00000234599.1","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"HCGIX-4,PERB11,HCGIX,HCGIX4","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":30053572,"end":30056871,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000123685.8","gene_symbol":"BATF3","gene_name":"basic leucine zipper ATF-like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:28915]","synonyms":"SNFT,JUNDM1,JDP1","biotype":"protein_coding","ncbi_id":"55509","summary":"This gene encodes a member of the basic leucine zipper protein family. The encoded protein functions as a transcriptional repressor when heterodimerizing with JUN. The protein may play a role in repression of interleukin-2 and matrix metalloproteinase-1 transcription.[provided by RefSeq, Feb 2009]","start":212686418,"end":212699985,"strand":-1,"description":"basic leucine zipper ATF-like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:28915]"}, {"versioned_ensembl_gene_id":"ENSG00000160058.18","gene_symbol":"BSDC1","gene_name":"BSD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25501]","synonyms":"RP4-811H24.7,FLJ10276","biotype":"protein_coding","ncbi_id":"55108","summary":null,"start":32365103,"end":32394731,"strand":-1,"description":"BSD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25501]"}, {"versioned_ensembl_gene_id":"ENSG00000237980.1","gene_symbol":"AL590648.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212653999,"end":212665434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253977.1","gene_symbol":"MTCO2P4","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480296","summary":null,"start":103091263,"end":103091509,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50349]"}, {"versioned_ensembl_gene_id":"ENSG00000234946.1","gene_symbol":"SDHCP3","gene_name":"succinate dehydrogenase complex subunit C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45178]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422591","summary":null,"start":23943846,"end":23944351,"strand":1,"description":"succinate dehydrogenase complex subunit C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45178]"}, {"versioned_ensembl_gene_id":"ENSG00000259436.1","gene_symbol":"AC010247.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42152569,"end":42157523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228398.3","gene_symbol":"HMGN2P25","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39392]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729687","summary":null,"start":141865012,"end":141865279,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:39392]"}, {"versioned_ensembl_gene_id":"ENSG00000271586.1","gene_symbol":"AC011894.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44601032,"end":44601487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197982.13","gene_symbol":"C1orf122","gene_name":"chromosome 1 open reading frame 122 [Source:HGNC Symbol;Acc:HGNC:24789]","synonyms":"FLJ45459","biotype":"protein_coding","ncbi_id":"127687","summary":null,"start":37806979,"end":37809454,"strand":1,"description":"chromosome 1 open reading frame 122 [Source:HGNC Symbol;Acc:HGNC:24789]"}, {"versioned_ensembl_gene_id":"ENSG00000018607.6","gene_symbol":"ZNF806","gene_name":"zinc finger protein 806 [Source:HGNC Symbol;Acc:HGNC:33228]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646915","summary":null,"start":132309309,"end":132318736,"strand":1,"description":"zinc finger protein 806 [Source:HGNC Symbol;Acc:HGNC:33228]"}, {"versioned_ensembl_gene_id":"ENSG00000249373.2","gene_symbol":"AC093879.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113031287,"end":113034551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254938.1","gene_symbol":"AP002833.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126920188,"end":126940659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226440.7","gene_symbol":"AL365214.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112236093,"end":112307009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216663.3","gene_symbol":"AL365214.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112325753,"end":112326749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254202.1","gene_symbol":"AC015522.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83912713,"end":84140283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224535.1","gene_symbol":"AC092803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":212466816,"end":212467743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143748.17","gene_symbol":"NVL","gene_name":"nuclear VCP-like [Source:HGNC Symbol;Acc:HGNC:8070]","synonyms":"NVL2","biotype":"protein_coding","ncbi_id":"4931","summary":"This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) superfamily. Multiple transcript variants encoding different isoforms have been found for this gene. Two encoded proteins, described as major and minor isoforms, have been localized to distinct regions of the nucleus. The largest encoded protein (major isoform) has been localized to the nucleolus and shown to participate in ribosome biosynthesis (PMID: 15469983, 16782053), while the minor isoform has been localized to the nucleoplasmin. [provided by RefSeq, Aug 2011]","start":224227334,"end":224330387,"strand":-1,"description":"nuclear VCP-like [Source:HGNC Symbol;Acc:HGNC:8070]"}, {"versioned_ensembl_gene_id":"ENSG00000280686.2","gene_symbol":"LINC01237","gene_name":"long intergenic non-protein coding RNA 1237 [Source:HGNC Symbol;Acc:HGNC:49793]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101927289","summary":null,"start":241881363,"end":241959696,"strand":1,"description":"long intergenic non-protein coding RNA 1237 [Source:HGNC Symbol;Acc:HGNC:49793]"}, {"versioned_ensembl_gene_id":"ENSG00000113194.12","gene_symbol":"FAF2","gene_name":"Fas associated factor family member 2 [Source:HGNC Symbol;Acc:HGNC:24666]","synonyms":"UBXD8,KIAA0887,ETEA,UBXN3B","biotype":"protein_coding","ncbi_id":"23197","summary":"The protein encoded by this gene is highly expressed in peripheral blood of patients with atopic dermatitis (AD), compared to normal individuals. It may play a role in regulating the resistance to apoptosis that is observed in T cells and eosinophils of AD patients. [provided by RefSeq, Jul 2008]","start":176447628,"end":176510074,"strand":1,"description":"Fas associated factor family member 2 [Source:HGNC Symbol;Acc:HGNC:24666]"}, {"versioned_ensembl_gene_id":"ENSG00000234975.6","gene_symbol":"FTH1P2","gene_name":"ferritin heavy chain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3989]","synonyms":"FTHL2","biotype":"processed_pseudogene","ncbi_id":"2497","summary":null,"start":228687415,"end":228687826,"strand":1,"description":"ferritin heavy chain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3989]"}, {"versioned_ensembl_gene_id":"ENSG00000051341.13","gene_symbol":"POLQ","gene_name":"DNA polymerase theta [Source:HGNC Symbol;Acc:HGNC:9186]","synonyms":"POLH","biotype":"protein_coding","ncbi_id":"10721","summary":null,"start":121431427,"end":121546641,"strand":-1,"description":"DNA polymerase theta [Source:HGNC Symbol;Acc:HGNC:9186]"}, {"versioned_ensembl_gene_id":"ENSG00000103343.12","gene_symbol":"ZNF174","gene_name":"zinc finger protein 174 [Source:HGNC Symbol;Acc:HGNC:12963]","synonyms":"ZSCAN8","biotype":"protein_coding","ncbi_id":"7727","summary":"This gene encodes a protein with three Cys2-His2-type zinc fingers in the carboxy-terminus, a putative nuclear localization signal, and an amino-terminus SCAN box which forms homodimers. This protein is believed to function as a transcriptional repressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]","start":3401235,"end":3409370,"strand":1,"description":"zinc finger protein 174 [Source:HGNC Symbol;Acc:HGNC:12963]"}, {"versioned_ensembl_gene_id":"ENSG00000230125.1","gene_symbol":"EEF1A1P39","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37917]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862850","summary":null,"start":30301823,"end":30302072,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:37917]"}, {"versioned_ensembl_gene_id":"ENSG00000279532.1","gene_symbol":"AC002094.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":28373673,"end":28374301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234511.8","gene_symbol":"C5orf58","gene_name":"chromosome 5 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:37272]","synonyms":null,"biotype":"protein_coding","ncbi_id":"133874","summary":null,"start":170232447,"end":170252575,"strand":1,"description":"chromosome 5 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:37272]"}, {"versioned_ensembl_gene_id":"ENSG00000047346.12","gene_symbol":"FAM214A","gene_name":"family with sequence similarity 214 member A [Source:HGNC Symbol;Acc:HGNC:25609]","synonyms":"KIAA1370,FLJ10980","biotype":"protein_coding","ncbi_id":"56204","summary":null,"start":52581317,"end":52709817,"strand":-1,"description":"family with sequence similarity 214 member A [Source:HGNC Symbol;Acc:HGNC:25609]"}, {"versioned_ensembl_gene_id":"ENSG00000188691.5","gene_symbol":"OR56A5","gene_name":"olfactory receptor family 56 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:14792]","synonyms":"OR56A5P","biotype":"protein_coding","ncbi_id":"390084","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Mar 2009]","start":5967177,"end":5968494,"strand":-1,"description":"olfactory receptor family 56 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:14792]"}, {"versioned_ensembl_gene_id":"ENSG00000277083.1","gene_symbol":"PRSS3P3","gene_name":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]","synonyms":"TRY3","biotype":"transcribed_unitary_pseudogene","ncbi_id":"136540","summary":null,"start":142287251,"end":142291597,"strand":-1,"description":"protease, serine 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43790]"}, {"versioned_ensembl_gene_id":"ENSG00000213579.3","gene_symbol":"AL096829.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75582099,"end":75582555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282291.1","gene_symbol":"SLC39A11","gene_name":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]","synonyms":"C17orf26","biotype":"protein_coding","ncbi_id":"201266","summary":null,"start":72837800,"end":72849806,"strand":-1,"description":"solute carrier family 39 member 11 [Source:HGNC Symbol;Acc:HGNC:14463]"}, {"versioned_ensembl_gene_id":"ENSG00000237913.1","gene_symbol":"FTLP19","gene_name":"ferritin light chain pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:37969]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873960","summary":null,"start":16071416,"end":16071809,"strand":-1,"description":"ferritin light chain pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:37969]"}, {"versioned_ensembl_gene_id":"ENSG00000282707.1","gene_symbol":"AC003042.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36574834,"end":36575697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264643.1","gene_symbol":"AC024614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33680577,"end":33680883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282662.1","gene_symbol":"AC093627.20","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138174,"end":151787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241221.2","gene_symbol":"MTND4LP17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42251]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075240","summary":null,"start":202617695,"end":202617987,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42251]"}, {"versioned_ensembl_gene_id":"ENSG00000224744.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31166192,"end":31170357,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000261600.1","gene_symbol":"AC233266.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91580336,"end":91580863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258893.1","gene_symbol":"SETP2","gene_name":"SET pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326277","summary":null,"start":51436038,"end":51436963,"strand":1,"description":"SET pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20032]"}, {"versioned_ensembl_gene_id":"ENSG00000260118.1","gene_symbol":"AL157700.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68013470,"end":68014901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213542.3","gene_symbol":"AC007000.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77115399,"end":77116192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251107.1","gene_symbol":"PDCD5P2","gene_name":"programmed cell death 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49886]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100527947","summary":null,"start":76280956,"end":76281267,"strand":1,"description":"programmed cell death 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49886]"}, {"versioned_ensembl_gene_id":"ENSG00000265479.6","gene_symbol":"DTX2P1-UPK3BP1-PMS2P11","gene_name":"DTX2P1-UPK3BP1-PMS2P11 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42360]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"441263","summary":"This locus represents naturally-occurring readthrough transcription spanning multiple pseudogenes: DTX2P1 (DTX2 pseudogene 1), UPK3BP1 (uroplakin 3B pseudogene 1), PMS2P11 (PMS1 homolog 2, mismatch repair system component pseudogene 11). Some transcripts may also extend to PMS2P9 (PMS1 homolog 2, mismatch repair system component pseudogene 9). The readthrough transcripts likely do not encode functional proteins. [provided by RefSeq, Jan 2016]","start":76959835,"end":77043775,"strand":1,"description":"DTX2P1-UPK3BP1-PMS2P11 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:42360]"}, {"versioned_ensembl_gene_id":"ENSG00000239465.1","gene_symbol":"AC090543.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64631109,"end":64631914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127586.16","gene_symbol":"CHTF18","gene_name":"chromosome transmission fidelity factor 18 [Source:HGNC Symbol;Acc:HGNC:18435]","synonyms":"Ctf18,CHL12,C321D2.4,C16orf41","biotype":"protein_coding","ncbi_id":"63922","summary":"This gene encodes a protein which is a component of a replication factor C (RFC) complex, which loads proliferating cell nuclear antigen (PCNA) on to DNA during the S phase of cell cycle. The encoded protein may interact with other proteins, including RFC complex 3, to form a clamp loader complex that plays a role in sister chromatid cohesion during metaphase-anaphase transition. [provided by RefSeq, Jan 2016]","start":788046,"end":800737,"strand":1,"description":"chromosome transmission fidelity factor 18 [Source:HGNC Symbol;Acc:HGNC:18435]"}, {"versioned_ensembl_gene_id":"ENSG00000253334.1","gene_symbol":"AC132219.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81791823,"end":81815714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182230.11","gene_symbol":"FAM153B","gene_name":"family with sequence similarity 153 member B [Source:HGNC Symbol;Acc:HGNC:27323]","synonyms":null,"biotype":"protein_coding","ncbi_id":"202134","summary":null,"start":176060689,"end":176132258,"strand":1,"description":"family with sequence similarity 153 member B [Source:HGNC Symbol;Acc:HGNC:27323]"}, {"versioned_ensembl_gene_id":"ENSG00000282744.1","gene_symbol":"AC246789.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16746309,"end":16752220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163281.11","gene_symbol":"GNPDA2","gene_name":"glucosamine-6-phosphate deaminase 2 [Source:HGNC Symbol;Acc:HGNC:21526]","synonyms":"SB52","biotype":"protein_coding","ncbi_id":"132789","summary":"The protein encoded by this gene is an allosteric enzyme that catalyzes the reversible reaction converting D-glucosamine-6-phosphate into D-fructose-6-phosphate and ammonium. Variations of this gene have been reported to be associated with influencing body mass index and susceptibility to obesity. A pseudogene of this gene is located on chromosome 9. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":44682200,"end":44726595,"strand":-1,"description":"glucosamine-6-phosphate deaminase 2 [Source:HGNC Symbol;Acc:HGNC:21526]"}, {"versioned_ensembl_gene_id":"ENSG00000251458.1","gene_symbol":"AC139491.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176124210,"end":176131461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229663.1","gene_symbol":"AL672296.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":248771635,"end":248773792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229081.1","gene_symbol":"LINC01165","gene_name":"long intergenic non-protein coding RNA 1165 [Source:HGNC Symbol;Acc:HGNC:49534]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128830","summary":null,"start":132520827,"end":132522449,"strand":-1,"description":"long intergenic non-protein coding RNA 1165 [Source:HGNC Symbol;Acc:HGNC:49534]"}, {"versioned_ensembl_gene_id":"ENSG00000248469.1","gene_symbol":"AC139491.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176049678,"end":176062021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277899.1","gene_symbol":"MLECP1","gene_name":"malectin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51122]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480317","summary":null,"start":44522366,"end":44523074,"strand":1,"description":"malectin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51122]"}, {"versioned_ensembl_gene_id":"ENSG00000248559.1","gene_symbol":"AC109454.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":134399495,"end":134401921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171943.11","gene_symbol":"SRGAP2C","gene_name":"SLIT-ROBO Rho GTPase activating protein 2C [Source:HGNC Symbol;Acc:HGNC:30584]","synonyms":"SRGAP2P1","biotype":"protein_coding","ncbi_id":"653464","summary":"This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. This human-specific locus resulted from segmental duplication of the SLIT-ROBO Rho GTPase activating protein 2B locus. The encoded protein lacks the GTPase activating protein domain compared to proteins encoded by SLIT-ROBO Rho GTPase activating protein 2, and acts antagonistically to these proteins in cortical neuron development. [provided by RefSeq, Dec 2012]","start":121184810,"end":121392822,"strand":1,"description":"SLIT-ROBO Rho GTPase activating protein 2C [Source:HGNC Symbol;Acc:HGNC:30584]"}, {"versioned_ensembl_gene_id":"ENSG00000235127.1","gene_symbol":"AC068286.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14886647,"end":14907664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177151.4","gene_symbol":"OR2T35","gene_name":"olfactory receptor family 2 subfamily T member 35 [Source:HGNC Symbol;Acc:HGNC:31257]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403244","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248636356,"end":248645278,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 35 [Source:HGNC Symbol;Acc:HGNC:31257]"}, {"versioned_ensembl_gene_id":"ENSG00000224630.2","gene_symbol":"AC234064.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144308834,"end":144309080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276380.2","gene_symbol":"UBE2NL","gene_name":"ubiquitin conjugating enzyme E2 N like (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:31710]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"389898","summary":"This gene is intronless and encodes a member of the ubiquitin-conjugating enzyme family. The protein product is 91% identical to ubiquitin-conjugating enzyme E2N, a multi-exon gene product. This locus represents a polymorphic pseudogene, where some individuals contain an allele that can encode a full-length protein, while others have a non-functional allele containing a premature stop codon (reference SNP rs237520) that truncates the coding sequence. [provided by RefSeq, Jun 2014]","start":143884071,"end":143885255,"strand":1,"description":"ubiquitin conjugating enzyme E2 N like (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:31710]"}, {"versioned_ensembl_gene_id":"ENSG00000105325.13","gene_symbol":"FZR1","gene_name":"fizzy and cell division cycle 20 related 1 [Source:HGNC Symbol;Acc:HGNC:24824]","synonyms":"KIAA1242,HCDH1,HCDH,FZR2,FZR,CDH1,CDC20C","biotype":"protein_coding","ncbi_id":"51343","summary":null,"start":3506273,"end":3538330,"strand":1,"description":"fizzy and cell division cycle 20 related 1 [Source:HGNC Symbol;Acc:HGNC:24824]"}, {"versioned_ensembl_gene_id":"ENSG00000227545.1","gene_symbol":"AC006455.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63349154,"end":63350059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196678.13","gene_symbol":"ERI2","gene_name":"ERI1 exoribonuclease family member 2 [Source:HGNC Symbol;Acc:HGNC:30541]","synonyms":"ZGRF5,MGC16943,KIAA1504,EXOD1","biotype":"protein_coding","ncbi_id":"112479","summary":null,"start":20780193,"end":20900349,"strand":-1,"description":"ERI1 exoribonuclease family member 2 [Source:HGNC Symbol;Acc:HGNC:30541]"}, {"versioned_ensembl_gene_id":"ENSG00000235036.4","gene_symbol":"AL035456.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10612861,"end":10614229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101204.16","gene_symbol":"CHRNA4","gene_name":"cholinergic receptor nicotinic alpha 4 subunit [Source:HGNC Symbol;Acc:HGNC:1958]","synonyms":"EBN,BFNC,EBN1","biotype":"protein_coding","ncbi_id":"1137","summary":"This gene encodes a nicotinic acetylcholine receptor, which belongs to a superfamily of ligand-gated ion channels that play a role in fast signal transmission at synapses. These pentameric receptors can bind acetylcholine, which causes an extensive change in conformation that leads to the opening of an ion-conducting channel across the plasma membrane. This protein is an integral membrane receptor subunit that can interact with either nAChR beta-2 or nAChR beta-4 to form a functional receptor. Mutations in this gene cause nocturnal frontal lobe epilepsy type 1. Polymorphisms in this gene that provide protection against nicotine addiction have been described. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":63343223,"end":63378401,"strand":-1,"description":"cholinergic receptor nicotinic alpha 4 subunit [Source:HGNC Symbol;Acc:HGNC:1958]"}, {"versioned_ensembl_gene_id":"ENSG00000230999.1","gene_symbol":"MTND5P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42270]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873198","summary":null,"start":112372647,"end":112373729,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42270]"}, {"versioned_ensembl_gene_id":"ENSG00000235601.1","gene_symbol":"BARX1-AS1","gene_name":"BARX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50673]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928040","summary":null,"start":93955597,"end":93959140,"strand":1,"description":"BARX1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50673]"}, {"versioned_ensembl_gene_id":"ENSG00000218792.2","gene_symbol":"HSPD1P16","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35128]","synonyms":"HSPD1-13P","biotype":"processed_pseudogene","ncbi_id":"100462985","summary":null,"start":152705735,"end":152706128,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:35128]"}, {"versioned_ensembl_gene_id":"ENSG00000275787.1","gene_symbol":"OR7G15P","gene_name":"olfactory receptor family 7 subfamily G member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:31313]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403300","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9122160,"end":9122492,"strand":-1,"description":"olfactory receptor family 7 subfamily G member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:31313]"}, {"versioned_ensembl_gene_id":"ENSG00000138759.18","gene_symbol":"FRAS1","gene_name":"Fraser extracellular matrix complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:19185]","synonyms":"FLJ14927,KIAA1500,FLJ22031","biotype":"protein_coding","ncbi_id":"80144","summary":"This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":78057570,"end":78544269,"strand":1,"description":"Fraser extracellular matrix complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:19185]"}, {"versioned_ensembl_gene_id":"ENSG00000161807.3","gene_symbol":"OR7G1","gene_name":"olfactory receptor family 7 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:8465]","synonyms":"OR7G1P,OR19-15","biotype":"protein_coding","ncbi_id":"125962","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9114828,"end":9115763,"strand":-1,"description":"olfactory receptor family 7 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:8465]"}, {"versioned_ensembl_gene_id":"ENSG00000102897.9","gene_symbol":"LYRM1","gene_name":"LYR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25074]","synonyms":"A211C6.1","biotype":"protein_coding","ncbi_id":"57149","summary":"The protein encoded by this gene belongs to the mitochondrial leucine/tyrosine/arginine motif family of proteins. Proteins of this family are short polypeptides that contain a leucine/tyrosine/arginine motif near the N-terminus. This gene is widely expressed with high levels in omental adipose tissue of obese individuals. In adipose tissue, the protein is localized to the nucleus where it promotes preadipocyte proliferation and lowers the rate of apoptosis to regulate adipose tissue homeostasis. Overexpression of this gene in adipocytes causes abnormal mitochondrial morphology and mitochondrial dysfunction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":20899868,"end":20925006,"strand":1,"description":"LYR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25074]"}, {"versioned_ensembl_gene_id":"ENSG00000236232.1","gene_symbol":"MTCYBP24","gene_name":"mitochondrially encoded cytochrome b pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51983]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075132","summary":null,"start":112374324,"end":112375429,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51983]"}, {"versioned_ensembl_gene_id":"ENSG00000249855.1","gene_symbol":"EEF1A1P19","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:37892]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421796","summary":null,"start":43495073,"end":43496454,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:37892]"}, {"versioned_ensembl_gene_id":"ENSG00000224679.1","gene_symbol":"MED15P4","gene_name":"mediator complex subunit 15 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48653]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100127989","summary":null,"start":131535187,"end":131536988,"strand":-1,"description":"mediator complex subunit 15 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48653]"}, {"versioned_ensembl_gene_id":"ENSG00000231364.2","gene_symbol":"LINC01712","gene_name":"long intergenic non-protein coding RNA 1712 [Source:HGNC Symbol;Acc:HGNC:52499]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927542","summary":null,"start":83445967,"end":83462687,"strand":1,"description":"long intergenic non-protein coding RNA 1712 [Source:HGNC Symbol;Acc:HGNC:52499]"}, {"versioned_ensembl_gene_id":"ENSG00000228254.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32789880,"end":32797319,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000233982.2","gene_symbol":"CR788234.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800074,"end":29800870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236243.2","gene_symbol":"RPL6P29","gene_name":"ribosomal protein L6 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36382]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392505","summary":null,"start":98251679,"end":98252543,"strand":1,"description":"ribosomal protein L6 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36382]"}, {"versioned_ensembl_gene_id":"ENSG00000261710.1","gene_symbol":"AC104417.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142089827,"end":142091619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283544.1","gene_symbol":"ABBA01000935.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91374236,"end":91513775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271024.1","gene_symbol":"HSPE1P19","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49338]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481675","summary":null,"start":90261414,"end":90261708,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:49338]"}, {"versioned_ensembl_gene_id":"ENSG00000139233.6","gene_symbol":"LLPH","gene_name":"LLP homolog, long-term synaptic facilitation [Source:HGNC Symbol;Acc:HGNC:28229]","synonyms":"MGC14817,hLLP,C12orf31","biotype":"protein_coding","ncbi_id":"84298","summary":null,"start":66116555,"end":66130768,"strand":-1,"description":"LLP homolog, long-term synaptic facilitation [Source:HGNC Symbol;Acc:HGNC:28229]"}, {"versioned_ensembl_gene_id":"ENSG00000226490.1","gene_symbol":"AC138647.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":141514638,"end":141518737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276111.3","gene_symbol":"SDCCAG8","gene_name":"serologically defined colon cancer antigen 8 [Source:HGNC Symbol;Acc:HGNC:10671]","synonyms":"SLSN7,NY-CO-8,NPHP10,CCCAP,BBS16","biotype":"protein_coding","ncbi_id":"10806","summary":"This gene encodes a centrosome associated protein. This protein may be involved in organizing the centrosome during interphase and mitosis. Mutations in this gene are associated with retinal-renal ciliopathy. [provided by RefSeq, Oct 2010]","start":243256056,"end":243500091,"strand":1,"description":"serologically defined colon cancer antigen 8 [Source:HGNC Symbol;Acc:HGNC:10671]"}, {"versioned_ensembl_gene_id":"ENSG00000279455.1","gene_symbol":"AC117500.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131620178,"end":131620765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258463.1","gene_symbol":"AC138701.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19899334,"end":19899559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257660.5","gene_symbol":"AC117498.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48789147,"end":48790535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206301.9","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32775123,"end":32780991,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000120885.21","gene_symbol":"CLU","gene_name":"clusterin [Source:HGNC Symbol;Acc:HGNC:2095]","synonyms":"SGP-2,KUB1,CLU2,CLU1,CLI,APOJ,TRPM-2,SP-40","biotype":"protein_coding","ncbi_id":"1191","summary":"The protein encoded by this gene is a secreted chaperone that can under some stress conditions also be found in the cell cytosol. It has been suggested to be involved in several basic biological events such as cell death, tumor progression, and neurodegenerative disorders. Alternate splicing results in both coding and non-coding variants.[provided by RefSeq, May 2011]","start":27596917,"end":27615031,"strand":-1,"description":"clusterin [Source:HGNC Symbol;Acc:HGNC:2095]"}, {"versioned_ensembl_gene_id":"ENSG00000276576.1","gene_symbol":"AL450489.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57029521,"end":57029988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275936.1","gene_symbol":"AC004263.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120224744,"end":120225421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282814.1","gene_symbol":"AC010724.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":82497719,"end":82513298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236667.1","gene_symbol":"AC104076.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180938830,"end":180939298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279243.1","gene_symbol":"AP000769.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65487241,"end":65488136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222022.1","gene_symbol":"AC112721.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237421420,"end":237425276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162006.9","gene_symbol":"MSLNL","gene_name":"mesothelin-like [Source:HGNC Symbol;Acc:HGNC:14170]","synonyms":"C16orf37,MPFL","biotype":"protein_coding","ncbi_id":"401827","summary":null,"start":769428,"end":783370,"strand":-1,"description":"mesothelin-like [Source:HGNC Symbol;Acc:HGNC:14170]"}, {"versioned_ensembl_gene_id":"ENSG00000078061.12","gene_symbol":"ARAF","gene_name":"A-Raf proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:646]","synonyms":"ARAF1","biotype":"protein_coding","ncbi_id":"369","summary":"This proto-oncogene belongs to the RAF subfamily of the Ser/Thr protein kinase family, and maybe involved in cell growth and development. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2012]","start":47561100,"end":47571920,"strand":1,"description":"A-Raf proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:646]"}, {"versioned_ensembl_gene_id":"ENSG00000227154.3","gene_symbol":"AL022721.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35443044,"end":35449866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267908.2","gene_symbol":"ZSCAN5DP","gene_name":"zinc finger and SCAN domain containing 5D pseudogene [Source:HGNC Symbol;Acc:HGNC:37706]","synonyms":"ZSCAN5DP,ZSCAN5D,ZNF495D","biotype":"unprocessed_pseudogene","ncbi_id":"646698","summary":null,"start":56244043,"end":56247482,"strand":1,"description":"zinc finger and SCAN domain containing 5D pseudogene [Source:HGNC Symbol;Acc:HGNC:37706]"}, {"versioned_ensembl_gene_id":"ENSG00000227152.6","gene_symbol":"OR2T7","gene_name":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]","synonyms":"OST723,OR2T7P","biotype":"polymorphic_pseudogene","ncbi_id":"81458","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248436359,"end":248444316,"strand":1,"description":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]"}, {"versioned_ensembl_gene_id":"ENSG00000250657.1","gene_symbol":"AC097451.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":43340875,"end":43345600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251689.1","gene_symbol":"AC079140.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":269866,"end":270175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228896.9","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"HLP,SKIV2,DDX13,SKI2W,170A,SKIV2L1","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31951734,"end":31962405,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000251188.1","gene_symbol":"AC079140.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":268982,"end":269531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237821.1","gene_symbol":"AC083873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133169416,"end":133170514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275339.1","gene_symbol":"Z99129.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122454358,"end":122454612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253540.5","gene_symbol":"FAM86HP","gene_name":"family with sequence similarity 86 member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:42359]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729375","summary":null,"start":130099092,"end":130111472,"strand":-1,"description":"family with sequence similarity 86 member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:42359]"}, {"versioned_ensembl_gene_id":"ENSG00000254939.1","gene_symbol":"AP003038.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98565074,"end":98566827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173727.12","gene_symbol":"AP000769.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65455258,"end":65466720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223513.1","gene_symbol":"ATP6V0E1P2","gene_name":"ATPase H+ transporting V0 subunit e1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874503","summary":null,"start":41859350,"end":41859594,"strand":-1,"description":"ATPase H+ transporting V0 subunit e1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41936]"}, {"versioned_ensembl_gene_id":"ENSG00000188811.13","gene_symbol":"NHLRC3","gene_name":"NHL repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:33751]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387921","summary":"This gene encodes a protein containing NCL-1, HT2A and Lin-41 (NHL) family repeats. Mammalian NHL-repeat containing proteins may be involved in a variety of enzymatic processes, including protein modification through ubiquitination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Aug 2012]","start":39038306,"end":39050109,"strand":1,"description":"NHL repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:33751]"}, {"versioned_ensembl_gene_id":"ENSG00000251287.8","gene_symbol":"ALG1L2","gene_name":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase like 2 [Source:HGNC Symbol;Acc:HGNC:37258]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644974","summary":null,"start":130081831,"end":130113227,"strand":1,"description":"ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase like 2 [Source:HGNC Symbol;Acc:HGNC:37258]"}, {"versioned_ensembl_gene_id":"ENSG00000267133.1","gene_symbol":"AC011518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32103583,"end":32106537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272249.1","gene_symbol":"AP003117.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97132835,"end":97133379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270077.1","gene_symbol":"AP003117.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":97144170,"end":97144723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215606.4","gene_symbol":"KRT18P35","gene_name":"keratin 18 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:33404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391584","summary":null,"start":141470634,"end":141471902,"strand":-1,"description":"keratin 18 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:33404]"}, {"versioned_ensembl_gene_id":"ENSG00000250397.2","gene_symbol":"AP006623.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":856880,"end":859795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253773.2","gene_symbol":"C8orf37-AS1","gene_name":"C8orf37 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50444]","synonyms":"tospeak","biotype":"lincRNA","ncbi_id":"100616530","summary":null,"start":95204456,"end":95810136,"strand":1,"description":"C8orf37 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50444]"}, {"versioned_ensembl_gene_id":"ENSG00000197067.6","gene_symbol":"OR2T32P","gene_name":"olfactory receptor family 2 subfamily T member 32 pseudogene [Source:HGNC Symbol;Acc:HGNC:31254]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"403241","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248083522,"end":248087522,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 32 pseudogene [Source:HGNC Symbol;Acc:HGNC:31254]"}, {"versioned_ensembl_gene_id":"ENSG00000087338.4","gene_symbol":"GMCL1","gene_name":"germ cell-less, spermatogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23843]","synonyms":"SPATA29,GCL1,FLJ13057,BTBD13","biotype":"protein_coding","ncbi_id":"64395","summary":"This gene encodes a nuclear envelope protein that appears to be involved in spermatogenesis, either directly or by influencing genes that play a more direct role in the process. This multi-exon locus is the homolog of the mouse and drosophila germ cell-less gene but the human genome also contains a single-exon locus on chromosome 5 that contains an open reading frame capable of encoding a highly-related protein. [provided by RefSeq, Jul 2008]","start":69829642,"end":69881396,"strand":1,"description":"germ cell-less, spermatogenesis associated 1 [Source:HGNC Symbol;Acc:HGNC:23843]"}, {"versioned_ensembl_gene_id":"ENSG00000270753.1","gene_symbol":"AP001836.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97086160,"end":97086682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227848.1","gene_symbol":"SUCLA2-AS1","gene_name":"SUCLA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39965]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929410","summary":null,"start":48001389,"end":48002552,"strand":1,"description":"SUCLA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39965]"}, {"versioned_ensembl_gene_id":"ENSG00000006740.16","gene_symbol":"ARHGAP44","gene_name":"Rho GTPase activating protein 44 [Source:HGNC Symbol;Acc:HGNC:29096]","synonyms":"RICH2,RICH-2,KIAA0672","biotype":"protein_coding","ncbi_id":"9912","summary":null,"start":12789539,"end":12991643,"strand":1,"description":"Rho GTPase activating protein 44 [Source:HGNC Symbol;Acc:HGNC:29096]"}, {"versioned_ensembl_gene_id":"ENSG00000241861.2","gene_symbol":"GAPDHP50","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:38556]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421236","summary":null,"start":89047442,"end":89048434,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:38556]"}, {"versioned_ensembl_gene_id":"ENSG00000255027.2","gene_symbol":"AP000842.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125903247,"end":125938916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229744.1","gene_symbol":"AC011998.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178017993,"end":178018465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124181.14","gene_symbol":"PLCG1","gene_name":"phospholipase C gamma 1 [Source:HGNC Symbol;Acc:HGNC:9065]","synonyms":"PLCgamma1,PLC148,PLC1,PLC-II,NCKAP3","biotype":"protein_coding","ncbi_id":"5335","summary":"The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of receptor-mediated tyrosine kinase activators. For example, when activated by SRC, the encoded protein causes the Ras guanine nucleotide exchange factor RasGRP1 to translocate to the Golgi, where it activates Ras. Also, this protein has been shown to be a major substrate for heparin-binding growth factor 1 (acidic fibroblast growth factor)-activated tyrosine kinase. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":41136960,"end":41196801,"strand":1,"description":"phospholipase C gamma 1 [Source:HGNC Symbol;Acc:HGNC:9065]"}, {"versioned_ensembl_gene_id":"ENSG00000255679.1","gene_symbol":"JRKL-AS1","gene_name":"JRKL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43670]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874053","summary":null,"start":96447132,"end":96506826,"strand":-1,"description":"JRKL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43670]"}, {"versioned_ensembl_gene_id":"ENSG00000073849.14","gene_symbol":"ST6GAL1","gene_name":"ST6 beta-galactoside alpha-2,6-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10860]","synonyms":"SIAT1","biotype":"protein_coding","ncbi_id":"6480","summary":"This gene encodes a member of glycosyltransferase family 29. The encoded protein is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The protein, which is normally found in the Golgi but can be proteolytically processed to a soluble form, is involved in the generation of the cell-surface carbohydrate determinants and differentiation antigens HB-6, CD75, and CD76. This gene has been incorrectly referred to as CD75. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":186930485,"end":187078553,"strand":1,"description":"ST6 beta-galactoside alpha-2,6-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10860]"}, {"versioned_ensembl_gene_id":"ENSG00000112033.13","gene_symbol":"PPARD","gene_name":"peroxisome proliferator activated receptor delta [Source:HGNC Symbol;Acc:HGNC:9235]","synonyms":"NUCII,NUC1,NR1C2,FAAR","biotype":"protein_coding","ncbi_id":"5467","summary":"This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) family. The encoded protein is thought to function as an integrator of transcriptional repression and nuclear receptor signaling. It may inhibit the ligand-induced transcriptional activity of peroxisome proliferator activated receptors alpha and gamma, though evidence for this effect is inconsistent. Expression of this gene in colorectal cancer cells may be variable but is typically relatively low. Knockout studies in mice suggested a role for this protein in myelination of the corpus callosum, lipid metabolism, differentiation, and epidermal cell proliferation. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Aug 2017]","start":35342558,"end":35428191,"strand":1,"description":"peroxisome proliferator activated receptor delta [Source:HGNC Symbol;Acc:HGNC:9235]"}, {"versioned_ensembl_gene_id":"ENSG00000075142.13","gene_symbol":"SRI","gene_name":"sorcin [Source:HGNC Symbol;Acc:HGNC:11292]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6717","summary":"This gene encodes a calcium-binding protein with multiple E-F hand domains that relocates from the cytoplasm to the sarcoplasmic reticulum in response to elevated calcium levels. In addition to regulating intracellular calcium homeostasis it also modulates excitation-contraction coupling in the heart. Alternative splicing results in multiple transcript variants encoding distinct proteins. Multiple pseudogenes exist for this gene. [provided by RefSeq, Mar 2012]","start":88205118,"end":88226993,"strand":-1,"description":"sorcin [Source:HGNC Symbol;Acc:HGNC:11292]"}, {"versioned_ensembl_gene_id":"ENSG00000282194.1","gene_symbol":"IGHV7-40","gene_name":"immunoglobulin heavy variable 7-40 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5666]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28381","summary":null,"start":106450046,"end":106450244,"strand":-1,"description":"immunoglobulin heavy variable 7-40 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5666]"}, {"versioned_ensembl_gene_id":"ENSG00000275426.1","gene_symbol":"AC253576.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":149738,"end":150317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268798.1","gene_symbol":"AC027307.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1440839,"end":1441938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187080.9","gene_symbol":"OR2AK2","gene_name":"olfactory receptor family 2 subfamily AK member 2 [Source:HGNC Symbol;Acc:HGNC:19569]","synonyms":"OR2AK1P","biotype":"protein_coding","ncbi_id":"391191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247965233,"end":247966386,"strand":1,"description":"olfactory receptor family 2 subfamily AK member 2 [Source:HGNC Symbol;Acc:HGNC:19569]"}, {"versioned_ensembl_gene_id":"ENSG00000138646.8","gene_symbol":"HERC5","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 5 [Source:HGNC Symbol;Acc:HGNC:24368]","synonyms":"CEB1","biotype":"protein_coding","ncbi_id":"51191","summary":"This gene is a member of the HERC family of ubiquitin ligases and encodes a protein with a HECT domain and five RCC1 repeats. Pro-inflammatory cytokines upregulate expression of this gene in endothelial cells. The protein localizes to the cytoplasm and perinuclear region and functions as an interferon-induced E3 protein ligase that mediates ISGylation of protein targets. The gene lies in a cluster of HERC family genes on chromosome 4. [provided by RefSeq, Jul 2008]","start":88457117,"end":88506163,"strand":1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 5 [Source:HGNC Symbol;Acc:HGNC:24368]"}, {"versioned_ensembl_gene_id":"ENSG00000188511.12","gene_symbol":"C22orf34","gene_name":"chromosome 22 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:28010]","synonyms":null,"biotype":"lincRNA","ncbi_id":"348645","summary":null,"start":49414524,"end":49657542,"strand":-1,"description":"chromosome 22 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:28010]"}, {"versioned_ensembl_gene_id":"ENSG00000279597.1","gene_symbol":"AL031593.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49534062,"end":49534926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224028.1","gene_symbol":"LINC01853","gene_name":"long intergenic non-protein coding RNA 1853 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000259076.1","gene_symbol":"AL049869.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64552694,"end":64596536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213046.4","gene_symbol":"EEF1A1P32","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:37909]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"730232","summary":null,"start":197688760,"end":197690627,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:37909]"}, {"versioned_ensembl_gene_id":"ENSG00000254271.1","gene_symbol":"AC022390.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60734342,"end":60741828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204882.3","gene_symbol":"GPR20","gene_name":"G protein-coupled receptor 20 [Source:HGNC Symbol;Acc:HGNC:4475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2843","summary":null,"start":141356500,"end":141367267,"strand":-1,"description":"G protein-coupled receptor 20 [Source:HGNC Symbol;Acc:HGNC:4475]"}, {"versioned_ensembl_gene_id":"ENSG00000163738.18","gene_symbol":"MTHFD2L","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like [Source:HGNC Symbol;Acc:HGNC:31865]","synonyms":"MGC72244","biotype":"protein_coding","ncbi_id":"441024","summary":null,"start":74114174,"end":74303099,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like [Source:HGNC Symbol;Acc:HGNC:31865]"}, {"versioned_ensembl_gene_id":"ENSG00000226939.1","gene_symbol":"AC062021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139366165,"end":139379147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224076.5","gene_symbol":"AC009487.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161422659,"end":161423577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184992.10","gene_symbol":"BRI3BP","gene_name":"BRI3 binding protein [Source:HGNC Symbol;Acc:HGNC:14251]","synonyms":"KG19,HCCRBP-3,HCCR-2,BNAS1","biotype":"protein_coding","ncbi_id":"140707","summary":null,"start":124993700,"end":125031231,"strand":1,"description":"BRI3 binding protein [Source:HGNC Symbol;Acc:HGNC:14251]"}, {"versioned_ensembl_gene_id":"ENSG00000234732.1","gene_symbol":"RPEP5","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44524]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481798","summary":null,"start":161931199,"end":161931466,"strand":-1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44524]"}, {"versioned_ensembl_gene_id":"ENSG00000243499.1","gene_symbol":"AC117500.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131667492,"end":131668246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280634.1","gene_symbol":"THRIL","gene_name":"TNF and HNRNPL related immunoregulatory long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49503]","synonyms":"TCONS_00020260,Linc1992,BRI3BP-AS1","biotype":"antisense_RNA","ncbi_id":"102659353","summary":null,"start":125025434,"end":125027410,"strand":-1,"description":"TNF and HNRNPL related immunoregulatory long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:49503]"}, {"versioned_ensembl_gene_id":"ENSG00000282377.1","gene_symbol":"AC011295.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":82380817,"end":82395723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273639.5","gene_symbol":"AL512310.12","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19499737,"end":19677926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197591.3","gene_symbol":"OR11L1","gene_name":"olfactory receptor family 11 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391189","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247840928,"end":247841896,"strand":-1,"description":"olfactory receptor family 11 subfamily L member 1 [Source:HGNC Symbol;Acc:HGNC:14998]"}, {"versioned_ensembl_gene_id":"ENSG00000260310.1","gene_symbol":"AC027277.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":10576499,"end":10578183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130997.16","gene_symbol":"POLN","gene_name":"DNA polymerase nu [Source:HGNC Symbol;Acc:HGNC:18870]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353497","summary":"This gene encodes a DNA polymerase type-A family member. The encoded protein plays a role in DNA repair and homologous recombination. This gene shares its 5' exons with some transcripts from overlapping GeneID: 79441, which encodes an augmentin-like protein complex subunit. [provided by RefSeq, Dec 2014]","start":2071918,"end":2242121,"strand":-1,"description":"DNA polymerase nu [Source:HGNC Symbol;Acc:HGNC:18870]"}, {"versioned_ensembl_gene_id":"ENSG00000258027.2","gene_symbol":"NF1P4","gene_name":"neurofibromin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:7769]","synonyms":"NF1L4","biotype":"unprocessed_pseudogene","ncbi_id":"100419029","summary":null,"start":19492281,"end":19501740,"strand":1,"description":"neurofibromin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:7769]"}, {"versioned_ensembl_gene_id":"ENSG00000233298.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29747862,"end":29748281,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000249926.2","gene_symbol":"AC117500.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131662596,"end":131664704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242138.1","gene_symbol":"BX927168.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32811743,"end":32814338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251610.2","gene_symbol":"AC083906.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130048143,"end":130055920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185040.13","gene_symbol":"SPDYE16","gene_name":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723555","summary":null,"start":76531319,"end":76541459,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E16 [Source:HGNC Symbol;Acc:HGNC:51512]"}, {"versioned_ensembl_gene_id":"ENSG00000276491.2","gene_symbol":"IGHV4-34","gene_name":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28395","summary":null,"start":106398342,"end":106398826,"strand":-1,"description":"immunoglobulin heavy variable 4-34 [Source:HGNC Symbol;Acc:HGNC:5650]"}, {"versioned_ensembl_gene_id":"ENSG00000282526.1","gene_symbol":"IGHV3-33-2","gene_name":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28433","summary":null,"start":106393788,"end":106394227,"strand":-1,"description":"immunoglobulin heavy variable 3-33-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5597]"}, {"versioned_ensembl_gene_id":"ENSG00000240895.1","gene_symbol":"AC117430.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110527482,"end":110529582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258706.1","gene_symbol":"AC127381.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19967414,"end":19968352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261400.1","gene_symbol":"AC011525.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31588040,"end":31595720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173464.14","gene_symbol":"RNASE11","gene_name":"ribonuclease A family member 11 (inactive) [Source:HGNC Symbol;Acc:HGNC:19269]","synonyms":"RAJ1,C14orf6","biotype":"protein_coding","ncbi_id":"122651","summary":null,"start":20583559,"end":20609884,"strand":-1,"description":"ribonuclease A family member 11 (inactive) [Source:HGNC Symbol;Acc:HGNC:19269]"}, {"versioned_ensembl_gene_id":"ENSG00000267465.6","gene_symbol":"AC011525.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31588196,"end":31593781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229658.1","gene_symbol":"PABPC1P9","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37991]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130338","summary":null,"start":16423943,"end":16426031,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37991]"}, {"versioned_ensembl_gene_id":"ENSG00000259427.2","gene_symbol":"DPPA5P2","gene_name":"developmental pluripotency associated 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43754]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100874380","summary":null,"start":45566776,"end":45567074,"strand":1,"description":"developmental pluripotency associated 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43754]"}, {"versioned_ensembl_gene_id":"ENSG00000259354.5","gene_symbol":"AC025580.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45448427,"end":45513767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255704.1","gene_symbol":"AC140063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131596857,"end":131597115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226556.2","gene_symbol":"NPM1P49","gene_name":"nucleophosmin 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45228]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422284","summary":null,"start":47438736,"end":47439774,"strand":-1,"description":"nucleophosmin 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:45228]"}, {"versioned_ensembl_gene_id":"ENSG00000166920.12","gene_symbol":"C15orf48","gene_name":"chromosome 15 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:29898]","synonyms":"NMES1","biotype":"protein_coding","ncbi_id":"84419","summary":"This gene was first identified in a study of human esophageal squamous cell carcinoma tissues. Levels of both the message and protein are reduced in carcinoma samples. In adult human tissues, this gene is expressed in the the esophagus, stomach, small intestine, colon and placenta. Alternatively spliced transcript variants that encode the same protein have been identified. [provided by RefSeq, Jun 2012]","start":45430529,"end":45448761,"strand":1,"description":"chromosome 15 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:29898]"}, {"versioned_ensembl_gene_id":"ENSG00000229771.2","gene_symbol":"AL035665.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40696499,"end":40698616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227942.1","gene_symbol":"FRMD8P1","gene_name":"FERM domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24690]","synonyms":"FKSG43","biotype":"processed_pseudogene","ncbi_id":"83957","summary":null,"start":65550898,"end":65552421,"strand":-1,"description":"FERM domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24690]"}, {"versioned_ensembl_gene_id":"ENSG00000230831.1","gene_symbol":"AC007349.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36838972,"end":36841373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071082.10","gene_symbol":"RPL31","gene_name":"ribosomal protein L31 [Source:HGNC Symbol;Acc:HGNC:10334]","synonyms":"L31","biotype":"protein_coding","ncbi_id":"6160","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L31E family of ribosomal proteins. It is located in the cytoplasm. Higher levels of expression of this gene in familial adenomatous polyps compared to matched normal tissues have been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":101001715,"end":101024032,"strand":1,"description":"ribosomal protein L31 [Source:HGNC Symbol;Acc:HGNC:10334]"}, {"versioned_ensembl_gene_id":"ENSG00000183208.12","gene_symbol":"GDPGP1","gene_name":"GDP-D-glucose phosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:34360]","synonyms":"C15orf58","biotype":"protein_coding","ncbi_id":"390637","summary":null,"start":90233808,"end":90245811,"strand":1,"description":"GDP-D-glucose phosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:34360]"}, {"versioned_ensembl_gene_id":"ENSG00000279418.1","gene_symbol":"LINC00244","gene_name":"long intergenic non-protein coding RNA 244 [Source:HGNC Symbol;Acc:HGNC:13245]","synonyms":"NCRNA00244,C7orf4","biotype":"lincRNA","ncbi_id":"64433","summary":null,"start":156540491,"end":156541103,"strand":1,"description":"long intergenic non-protein coding RNA 244 [Source:HGNC Symbol;Acc:HGNC:13245]"}, {"versioned_ensembl_gene_id":"ENSG00000111785.19","gene_symbol":"RIC8B","gene_name":"RIC8 guanine nucleotide exchange factor B [Source:HGNC Symbol;Acc:HGNC:25555]","synonyms":"RIC8,hSyn,FLJ10620","biotype":"protein_coding","ncbi_id":"55188","summary":null,"start":106774595,"end":106889316,"strand":1,"description":"RIC8 guanine nucleotide exchange factor B [Source:HGNC Symbol;Acc:HGNC:25555]"}, {"versioned_ensembl_gene_id":"ENSG00000257918.1","gene_symbol":"AC079385.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106714924,"end":106733066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136813.14","gene_symbol":"KIAA0368","gene_name":"KIAA0368 [Source:HGNC Symbol;Acc:HGNC:29020]","synonyms":"FLJ22036,ECM29","biotype":"protein_coding","ncbi_id":"23392","summary":null,"start":111360692,"end":111484745,"strand":-1,"description":"KIAA0368 [Source:HGNC Symbol;Acc:HGNC:29020]"}, {"versioned_ensembl_gene_id":"ENSG00000261502.3","gene_symbol":"AC040174.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63056786,"end":63129654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229043.2","gene_symbol":"AC091729.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1160374,"end":1165267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185960.13","gene_symbol":"SHOX","gene_name":"short stature homeobox [Source:HGNC Symbol;Acc:HGNC:10853]","synonyms":"SS,SHOXY,PHOG,GCFX","biotype":"protein_coding","ncbi_id":"6473","summary":"This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]","start":624344,"end":659411,"strand":1,"description":"short stature homeobox [Source:HGNC Symbol;Acc:HGNC:10853]"}, {"versioned_ensembl_gene_id":"ENSG00000229232.6","gene_symbol":"KRT18P53","gene_name":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478925","summary":null,"start":545236,"end":545352,"strand":-1,"description":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]"}, {"versioned_ensembl_gene_id":"ENSG00000267096.1","gene_symbol":"AC008735.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55670632,"end":55672069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224357.1","gene_symbol":"ATG3P1","gene_name":"autophagy related 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31123]","synonyms":"dJ54G6.1,ATG3P","biotype":"processed_pseudogene","ncbi_id":"100135756","summary":null,"start":39329014,"end":39329924,"strand":-1,"description":"autophagy related 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31123]"}, {"versioned_ensembl_gene_id":"ENSG00000163938.16","gene_symbol":"GNL3","gene_name":"G protein nucleolar 3 [Source:HGNC Symbol;Acc:HGNC:29931]","synonyms":"NS,MGC800,E2IG3,C77032","biotype":"protein_coding","ncbi_id":"26354","summary":"The protein encoded by this gene may interact with p53 and may be involved in tumorigenesis. The encoded protein also appears to be important for stem cell proliferation. This protein is found in both the nucleus and nucleolus. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":52681156,"end":52694492,"strand":1,"description":"G protein nucleolar 3 [Source:HGNC Symbol;Acc:HGNC:29931]"}, {"versioned_ensembl_gene_id":"ENSG00000184216.13","gene_symbol":"IRAK1","gene_name":"interleukin 1 receptor associated kinase 1 [Source:HGNC Symbol;Acc:HGNC:6112]","synonyms":"pelle,IRAK","biotype":"protein_coding","ncbi_id":"3654","summary":"This gene encodes the interleukin-1 receptor-associated kinase 1, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. This gene is partially responsible for IL1-induced upregulation of the transcription factor NF-kappa B. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":154010500,"end":154019980,"strand":-1,"description":"interleukin 1 receptor associated kinase 1 [Source:HGNC Symbol;Acc:HGNC:6112]"}, {"versioned_ensembl_gene_id":"ENSG00000275956.1","gene_symbol":"AC104446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52732547,"end":52733867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224251.6","gene_symbol":"AL391427.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4995488,"end":4997380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206483.5","gene_symbol":"TXNRD3NB","gene_name":"thioredoxin reductase 3 neighbor [Source:HGNC Symbol;Acc:HGNC:33870]","synonyms":"TR2IT1,TXNRD3NT1,TXNRD3IT1,TR2IT1,TXNRD3NT1,TXNRD3IT1","biotype":"protein_coding","ncbi_id":"645840","summary":null,"start":126571789,"end":126572636,"strand":-1,"description":"thioredoxin reductase 3 neighbor [Source:HGNC Symbol;Acc:HGNC:33870]"}, {"versioned_ensembl_gene_id":"ENSG00000060762.18","gene_symbol":"MPC1","gene_name":"mitochondrial pyruvate carrier 1 [Source:HGNC Symbol;Acc:HGNC:21606]","synonyms":"SLC54A1,dJ68L15.3,CGI-129,BRP44L","biotype":"protein_coding","ncbi_id":"51660","summary":"The protein encoded by this gene is part of an MPC1/MPC2 heterodimer that is responsible for transporting pyruvate into mitochondria. The encoded protein is found in the inner mitochondrial membrane. Defects in this gene are a cause of mitochondrial pyruvate carrier deficiency. Several transcript variants, some protein coding and one non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012]","start":166364919,"end":166383013,"strand":-1,"description":"mitochondrial pyruvate carrier 1 [Source:HGNC Symbol;Acc:HGNC:21606]"}, {"versioned_ensembl_gene_id":"ENSG00000233885.7","gene_symbol":"YEATS2-AS1","gene_name":"YEATS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41101]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874113","summary":null,"start":183806457,"end":183810783,"strand":-1,"description":"YEATS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41101]"}, {"versioned_ensembl_gene_id":"ENSG00000275306.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54905771,"end":54920219,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000273407.1","gene_symbol":"AC069294.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99766543,"end":99766892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174564.12","gene_symbol":"IL20RB","gene_name":"interleukin 20 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:6004]","synonyms":"MGC34923,IL-20R2,FNDC6,DIRS1","biotype":"protein_coding","ncbi_id":"53833","summary":"IL20RB and IL20RA (MIM 605620) form a heterodimeric receptor for interleukin-20 (IL20; MIM 605619) (Blumberg et al., 2001 [PubMed 11163236]).[supplied by OMIM, Feb 2009]","start":136946230,"end":137011085,"strand":1,"description":"interleukin 20 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:6004]"}, {"versioned_ensembl_gene_id":"ENSG00000270964.1","gene_symbol":"AC016355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67541072,"end":67542604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105127.8","gene_symbol":"AKAP8","gene_name":"A-kinase anchoring protein 8 [Source:HGNC Symbol;Acc:HGNC:378]","synonyms":"DKFZp586B1222,AKAP95","biotype":"protein_coding","ncbi_id":"10270","summary":"This gene encodes a member of the A-kinase anchor protein family. A-kinase anchor proteins are scaffold proteins that contain a binding domain for the RI/RII subunit of protein kinase A (PKA) and recruit PKA and other signaling molecules to specific subcellular locations. This gene encodes a nuclear A-kinase anchor protein that binds to the RII alpha subunit of PKA and may play a role in chromosome condensation during mitosis by targeting PKA and the condensin complex to chromatin. A pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, May 2011]","start":15353385,"end":15379798,"strand":-1,"description":"A-kinase anchoring protein 8 [Source:HGNC Symbol;Acc:HGNC:378]"}, {"versioned_ensembl_gene_id":"ENSG00000228089.1","gene_symbol":"PNKDP1","gene_name":"PNKD pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49628]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506715","summary":null,"start":131803312,"end":131803741,"strand":-1,"description":"PNKD pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49628]"}, {"versioned_ensembl_gene_id":"ENSG00000173581.7","gene_symbol":"CCDC106","gene_name":"coiled-coil domain containing 106 [Source:HGNC Symbol;Acc:HGNC:30181]","synonyms":"HSU79303","biotype":"protein_coding","ncbi_id":"29903","summary":null,"start":55641062,"end":55653161,"strand":1,"description":"coiled-coil domain containing 106 [Source:HGNC Symbol;Acc:HGNC:30181]"}, {"versioned_ensembl_gene_id":"ENSG00000215270.3","gene_symbol":"AP000523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15854195,"end":15855243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280273.2","gene_symbol":"AF131216.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11283481,"end":11285068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259984.1","gene_symbol":"AL928711.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25336429,"end":25337465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261349.1","gene_symbol":"AL031432.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25266102,"end":25267136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099721.13","gene_symbol":"AMELY","gene_name":"amelogenin, Y-linked [Source:HGNC Symbol;Acc:HGNC:462]","synonyms":"AMGL","biotype":"protein_coding","ncbi_id":"266","summary":"This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in a related gene on chromosome X cause X-linked amelogenesis imperfecta. [provided by RefSeq, Jul 2008]","start":6865918,"end":6874027,"strand":-1,"description":"amelogenin, Y-linked [Source:HGNC Symbol;Acc:HGNC:462]"}, {"versioned_ensembl_gene_id":"ENSG00000078589.12","gene_symbol":"P2RY10","gene_name":"purinergic receptor P2Y10 [Source:HGNC Symbol;Acc:HGNC:19906]","synonyms":"P2Y10","biotype":"protein_coding","ncbi_id":"27334","summary":"The protein encoded by this gene belongs to the family of G-protein coupled receptors that are preferentially activated by adenosine and uridine nucleotides. There is a pseudogene for this gene nearby on chromosome X. Multiple alternatively spliced transcripts have been observed. [provided by RefSeq, Apr 2016]","start":78945332,"end":78961954,"strand":1,"description":"purinergic receptor P2Y10 [Source:HGNC Symbol;Acc:HGNC:19906]"}, {"versioned_ensembl_gene_id":"ENSG00000254365.1","gene_symbol":"AC091820.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167287320,"end":167294273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269244.1","gene_symbol":"RPL23AP78","gene_name":"ribosomal protein L23a pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:35518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271624","summary":null,"start":8728735,"end":8729204,"strand":-1,"description":"ribosomal protein L23a pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:35518]"}, {"versioned_ensembl_gene_id":"ENSG00000279623.1","gene_symbol":"AL359697.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21865335,"end":21865921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181786.4","gene_symbol":"ACTL9","gene_name":"actin like 9 [Source:HGNC Symbol;Acc:HGNC:28494]","synonyms":"MGC33407","biotype":"protein_coding","ncbi_id":"284382","summary":null,"start":8697397,"end":8698822,"strand":-1,"description":"actin like 9 [Source:HGNC Symbol;Acc:HGNC:28494]"}, {"versioned_ensembl_gene_id":"ENSG00000230130.1","gene_symbol":"MTND2P39","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075312","summary":null,"start":143434517,"end":143435280,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:52070]"}, {"versioned_ensembl_gene_id":"ENSG00000106415.12","gene_symbol":"GLCCI1","gene_name":"glucocorticoid induced 1 [Source:HGNC Symbol;Acc:HGNC:18713]","synonyms":"TSSN1,GIG18,FAM117C","biotype":"protein_coding","ncbi_id":"113263","summary":"This gene encodes a protein of unknown function. Expression of this gene is induced by glucocorticoids and may be an early marker for glucocorticoid-induced apoptosis. Single nucleotide polymorphisms in this gene are associated with a decreased response to inhaled glucocorticoids in asthmatic patients. [provided by RefSeq, Feb 2012]","start":7968794,"end":8094272,"strand":1,"description":"glucocorticoid induced 1 [Source:HGNC Symbol;Acc:HGNC:18713]"}, {"versioned_ensembl_gene_id":"ENSG00000248659.1","gene_symbol":"AC023162.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":129632019,"end":129632492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272856.1","gene_symbol":"AC112250.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87460807,"end":87462280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188158.14","gene_symbol":"NHS","gene_name":"NHS actin remodeling regulator [Source:HGNC Symbol;Acc:HGNC:7820]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4810","summary":"This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014]","start":17375420,"end":17735994,"strand":1,"description":"NHS actin remodeling regulator [Source:HGNC Symbol;Acc:HGNC:7820]"}, {"versioned_ensembl_gene_id":"ENSG00000254097.1","gene_symbol":"IGKV3D-25","gene_name":"immunoglobulin kappa variable 3D-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5826]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28873","summary":null,"start":89989987,"end":89990221,"strand":1,"description":"immunoglobulin kappa variable 3D-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5826]"}, {"versioned_ensembl_gene_id":"ENSG00000249649.1","gene_symbol":"MRPS33P2","gene_name":"mitochondrial ribosomal protein S33 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29765]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359775","summary":null,"start":38006784,"end":38007105,"strand":-1,"description":"mitochondrial ribosomal protein S33 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29765]"}, {"versioned_ensembl_gene_id":"ENSG00000114248.9","gene_symbol":"LRRC31","gene_name":"leucine rich repeat containing 31 [Source:HGNC Symbol;Acc:HGNC:26261]","synonyms":"FLJ23259","biotype":"protein_coding","ncbi_id":"79782","summary":null,"start":169839179,"end":169869930,"strand":-1,"description":"leucine rich repeat containing 31 [Source:HGNC Symbol;Acc:HGNC:26261]"}, {"versioned_ensembl_gene_id":"ENSG00000166452.11","gene_symbol":"AKIP1","gene_name":"A-kinase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:1170]","synonyms":"C11orf17,BCA3","biotype":"protein_coding","ncbi_id":"56672","summary":"This gene encodes a nuclear protein that interacts with protein kinase A catalytic subunit, and regulates the effect of the cAMP-dependent protein kinase signaling pathway on the NF-kappa-B activation cascade. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]","start":8911139,"end":8920084,"strand":1,"description":"A-kinase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:1170]"}, {"versioned_ensembl_gene_id":"ENSG00000178691.10","gene_symbol":"SUZ12","gene_name":"SUZ12 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:17101]","synonyms":"KIAA0160,JJAZ1,CHET9","biotype":"protein_coding","ncbi_id":"23512","summary":"This zinc finger gene has been identified at the breakpoints of a recurrent chromosomal translocation reported in endometrial stromal sarcoma. Recombination of these breakpoints results in the fusion of this gene and JAZF1. The protein encoded by this gene contains a zinc finger domain in the C terminus of the coding region. [provided by RefSeq, Jul 2009]","start":31937018,"end":32001045,"strand":1,"description":"SUZ12 polycomb repressive complex 2 subunit [Source:HGNC Symbol;Acc:HGNC:17101]"}, {"versioned_ensembl_gene_id":"ENSG00000225352.1","gene_symbol":"RPL31P53","gene_name":"ribosomal protein L31 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:35749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271477","summary":null,"start":57391171,"end":57391518,"strand":-1,"description":"ribosomal protein L31 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:35749]"}, {"versioned_ensembl_gene_id":"ENSG00000267576.1","gene_symbol":"AC011472.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11322156,"end":11324195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197557.6","gene_symbol":"TTC30A","gene_name":"tetratricopeptide repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:25853]","synonyms":"IFT70A,FLJ13946","biotype":"protein_coding","ncbi_id":"92104","summary":null,"start":177612992,"end":177618966,"strand":-1,"description":"tetratricopeptide repeat domain 30A [Source:HGNC Symbol;Acc:HGNC:25853]"}, {"versioned_ensembl_gene_id":"ENSG00000183401.11","gene_symbol":"CCDC159","gene_name":"coiled-coil domain containing 159 [Source:HGNC Symbol;Acc:HGNC:26996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126075","summary":null,"start":11344684,"end":11354944,"strand":1,"description":"coiled-coil domain containing 159 [Source:HGNC Symbol;Acc:HGNC:26996]"}, {"versioned_ensembl_gene_id":"ENSG00000224953.1","gene_symbol":"SRIP3","gene_name":"sorcin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38735]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861435","summary":null,"start":6718962,"end":6719180,"strand":-1,"description":"sorcin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38735]"}, {"versioned_ensembl_gene_id":"ENSG00000260305.1","gene_symbol":"NTRK3-AS1","gene_name":"NTRK3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27532]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283738","summary":null,"start":88252730,"end":88271066,"strand":1,"description":"NTRK3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27532]"}, {"versioned_ensembl_gene_id":"ENSG00000237655.1","gene_symbol":"AC073834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177603089,"end":177618572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259183.1","gene_symbol":"MED28P6","gene_name":"mediator complex subunit 28 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45083]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480808","summary":null,"start":88143935,"end":88144165,"strand":-1,"description":"mediator complex subunit 28 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45083]"}, {"versioned_ensembl_gene_id":"ENSG00000248210.1","gene_symbol":"LINC02355","gene_name":"long intergenic non-protein coding RNA 2355 [Source:HGNC Symbol;Acc:HGNC:53277]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927849","summary":null,"start":149154295,"end":149278123,"strand":1,"description":"long intergenic non-protein coding RNA 2355 [Source:HGNC Symbol;Acc:HGNC:53277]"}, {"versioned_ensembl_gene_id":"ENSG00000110057.7","gene_symbol":"UNC93B1","gene_name":"unc-93 homolog B1 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13481]","synonyms":"UNC93","biotype":"protein_coding","ncbi_id":"81622","summary":"This gene encodes a protein that is involved in innate and adaptive immune response by regulating toll-like receptor signaling. The encoded protein traffics nucleotide sensing toll-like receptors to the endolysosome from the endoplasmic reticulum. Deficiency of the encoded protein has been associated with herpes simplex encephalitis. [provided by RefSeq, Feb 2014]","start":67991104,"end":68004982,"strand":-1,"description":"unc-93 homolog B1 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13481]"}, {"versioned_ensembl_gene_id":"ENSG00000231623.2","gene_symbol":"BX682535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31518863,"end":31519442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250252.1","gene_symbol":"LINC02430","gene_name":"long intergenic non-protein coding RNA 2430 [Source:HGNC Symbol;Acc:HGNC:53361]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986319","summary":null,"start":149147802,"end":149149780,"strand":-1,"description":"long intergenic non-protein coding RNA 2430 [Source:HGNC Symbol;Acc:HGNC:53361]"}, {"versioned_ensembl_gene_id":"ENSG00000233641.9","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30636880,"end":30642942,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000243988.1","gene_symbol":"AC012181.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56906534,"end":56906956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176946.11","gene_symbol":"THAP4","gene_name":"THAP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23187]","synonyms":"CGI-36","biotype":"protein_coding","ncbi_id":"51078","summary":null,"start":241584405,"end":241637449,"strand":-1,"description":"THAP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23187]"}, {"versioned_ensembl_gene_id":"ENSG00000172716.16","gene_symbol":"SLFN11","gene_name":"schlafen family member 11 [Source:HGNC Symbol;Acc:HGNC:26633]","synonyms":"FLJ34922","biotype":"protein_coding","ncbi_id":"91607","summary":null,"start":35350305,"end":35373701,"strand":-1,"description":"schlafen family member 11 [Source:HGNC Symbol;Acc:HGNC:26633]"}, {"versioned_ensembl_gene_id":"ENSG00000253562.1","gene_symbol":"AC107909.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99091738,"end":99094060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253912.1","gene_symbol":"AC018442.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99804159,"end":99804341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274528.1","gene_symbol":"AC090970.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52017167,"end":52018032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233461.5","gene_symbol":"AL445524.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":231522388,"end":231528556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233063.2","gene_symbol":"SAR1AP4","gene_name":"secretion associated Ras related GTPase 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37638]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132322","summary":null,"start":75884546,"end":75885136,"strand":1,"description":"secretion associated Ras related GTPase 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37638]"}, {"versioned_ensembl_gene_id":"ENSG00000254563.1","gene_symbol":"AP002768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78749250,"end":78756480,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239381.6","gene_symbol":"AC125613.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181534177,"end":181700611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231321.9","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"H-2RIIBP,RCoR-1,NR2B2","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33347482,"end":33354568,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000182223.7","gene_symbol":"ZAR1","gene_name":"zygote arrest 1 [Source:HGNC Symbol;Acc:HGNC:20436]","synonyms":"Z3CXXC6","biotype":"protein_coding","ncbi_id":"326340","summary":"This maternal effect gene is oocyte-specific and encodes a protein that is thought to function in the initiation of embryogenesis. A similar protein in mouse is required for female fertility. [provided by RefSeq, Jul 2013]","start":48490252,"end":48494389,"strand":1,"description":"zygote arrest 1 [Source:HGNC Symbol;Acc:HGNC:20436]"}, {"versioned_ensembl_gene_id":"ENSG00000266693.1","gene_symbol":"OR4K8P","gene_name":"olfactory receptor family 4 subfamily K member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:14787]","synonyms":"OR4K9P","biotype":"unprocessed_pseudogene","ncbi_id":"390836","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14613137,"end":14614184,"strand":1,"description":"olfactory receptor family 4 subfamily K member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:14787]"}, {"versioned_ensembl_gene_id":"ENSG00000132437.17","gene_symbol":"DDC","gene_name":"dopa decarboxylase [Source:HGNC Symbol;Acc:HGNC:2719]","synonyms":"AADC","biotype":"protein_coding","ncbi_id":"1644","summary":"The encoded protein catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine. Defects in this gene are the cause of aromatic L-amino-acid decarboxylase deficiency (AADCD). AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2011]","start":50458436,"end":50565457,"strand":-1,"description":"dopa decarboxylase [Source:HGNC Symbol;Acc:HGNC:2719]"}, {"versioned_ensembl_gene_id":"ENSG00000102871.15","gene_symbol":"TRADD","gene_name":"TNFRSF1A associated via death domain [Source:HGNC Symbol;Acc:HGNC:12030]","synonyms":"Hs.89862","biotype":"protein_coding","ncbi_id":"8717","summary":"The protein encoded by this gene is a death domain containing adaptor molecule that interacts with TNFRSF1A/TNFR1 and mediates programmed cell death signaling and NF-kappaB activation. This protein binds adaptor protein TRAF2, reduces the recruitment of inhibitor-of-apoptosis proteins (IAPs) by TRAF2, and thus suppresses TRAF2 mediated apoptosis. This protein can also interact with receptor TNFRSF6/FAS and adaptor protein FADD/MORT1, and is involved in the Fas-induced cell death pathway. [provided by RefSeq, Jul 2008]","start":67154180,"end":67160298,"strand":-1,"description":"TNFRSF1A associated via death domain [Source:HGNC Symbol;Acc:HGNC:12030]"}, {"versioned_ensembl_gene_id":"ENSG00000166926.8","gene_symbol":"MS4A6E","gene_name":"membrane spanning 4-domains A6E [Source:HGNC Symbol;Acc:HGNC:14285]","synonyms":null,"biotype":"protein_coding","ncbi_id":"245802","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. The gene encoding this protein is localized to 11q12.3, among a cluster of family members. [provided by RefSeq, Jul 2008]","start":60334831,"end":60396596,"strand":1,"description":"membrane spanning 4-domains A6E [Source:HGNC Symbol;Acc:HGNC:14285]"}, {"versioned_ensembl_gene_id":"ENSG00000254748.1","gene_symbol":"HNRNPCP8","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131842","summary":null,"start":87024583,"end":87025777,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48819]"}, {"versioned_ensembl_gene_id":"ENSG00000267055.1","gene_symbol":"AC007001.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20096137,"end":20130475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163827.12","gene_symbol":"LRRC2","gene_name":"leucine rich repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14676]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79442","summary":"This gene encodes a member of the leucine-rich repeat-containing family of proteins, which function in diverse biological pathways. This family member may possibly be a nuclear protein. Similarity to the RAS suppressor protein, as well as expression down-regulation observed in tumor cells, suggests that it may function as a tumor suppressor. The gene is located in the chromosome 3 common eliminated region 1 (C3CER1), a 1.4 Mb region that is commonly deleted in diverse tumors. A related pseudogene has been identified on chromosome 2. [provided by RefSeq, Sep 2011]","start":46515423,"end":46580099,"strand":-1,"description":"leucine rich repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:14676]"}, {"versioned_ensembl_gene_id":"ENSG00000132549.18","gene_symbol":"VPS13B","gene_name":"vacuolar protein sorting 13 homolog B [Source:HGNC Symbol;Acc:HGNC:2183]","synonyms":"COH1,CHS1","biotype":"protein_coding","ncbi_id":"157680","summary":"This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":99013266,"end":99877580,"strand":1,"description":"vacuolar protein sorting 13 homolog B [Source:HGNC Symbol;Acc:HGNC:2183]"}, {"versioned_ensembl_gene_id":"ENSG00000176720.5","gene_symbol":"BOK","gene_name":"BOK, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:1087]","synonyms":"MGC4631,BOKL,BCL2L9","biotype":"protein_coding","ncbi_id":"666","summary":"The protein encoded by this gene belongs to the BCL2 family, members of which form homo- or heterodimers, and act as anti- or proapoptotic regulators that are involved in a wide variety of cellular processes. Studies in rat show that this protein has restricted expression in reproductive tissues, interacts strongly with some antiapoptotic BCL2 proteins, not at all with proapoptotic BCL2 proteins, and induces apoptosis in transfected cells. Thus, this protein represents a proapoptotic member of the BCL2 family. [provided by RefSeq, Sep 2011]","start":241551424,"end":241574138,"strand":1,"description":"BOK, BCL2 family apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:1087]"}, {"versioned_ensembl_gene_id":"ENSG00000213061.2","gene_symbol":"PFN1P11","gene_name":"profilin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873784","summary":null,"start":102838011,"end":102845473,"strand":-1,"description":"profilin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42994]"}, {"versioned_ensembl_gene_id":"ENSG00000254020.1","gene_symbol":"AC104211.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92723024,"end":92725111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251634.2","gene_symbol":"AC145138.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71102898,"end":71128753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090470.14","gene_symbol":"PDCD7","gene_name":"programmed cell death 7 [Source:HGNC Symbol;Acc:HGNC:8767]","synonyms":"HES18,ES18","biotype":"protein_coding","ncbi_id":"10081","summary":"This gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP), which is a component of the minor U12-type spliceosome responsible for catalyzing pre-mRNA splicing of U12-type introns. [provided by RefSeq, Dec 2010]","start":65117379,"end":65133836,"strand":-1,"description":"programmed cell death 7 [Source:HGNC Symbol;Acc:HGNC:8767]"}, {"versioned_ensembl_gene_id":"ENSG00000255294.2","gene_symbol":"OR4A50P","gene_name":"olfactory receptor family 4 subfamily A member 50 pseudogene [Source:HGNC Symbol;Acc:HGNC:31269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403256","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55475943,"end":55478512,"strand":1,"description":"olfactory receptor family 4 subfamily A member 50 pseudogene [Source:HGNC Symbol;Acc:HGNC:31269]"}, {"versioned_ensembl_gene_id":"ENSG00000205277.9","gene_symbol":"MUC12","gene_name":"mucin 12, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7510]","synonyms":"MUC11","biotype":"protein_coding","ncbi_id":"10071","summary":"This gene encodes an integral membrane glycoprotein that is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces and have been implicated in epithelial renewal and differentiation. These glycoproteins also play a role in intracellular signaling. This protein is expressed on the apical membrane surface of epithelial cells that line the mucosal surfaces of many different tissues including the colon, pancreas, prostate, and uterus. The expression of this gene is downregulated in colorectal cancer tissue. [provided by RefSeq, Apr 2017]","start":100969623,"end":101018949,"strand":1,"description":"mucin 12, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7510]"}, {"versioned_ensembl_gene_id":"ENSG00000145309.5","gene_symbol":"CABS1","gene_name":"calcium binding protein, spermatid associated 1 [Source:HGNC Symbol;Acc:HGNC:30710]","synonyms":"NYD-SP26,FLJ32897,CLPH,C4orf35","biotype":"protein_coding","ncbi_id":"85438","summary":null,"start":70334966,"end":70337116,"strand":1,"description":"calcium binding protein, spermatid associated 1 [Source:HGNC Symbol;Acc:HGNC:30710]"}, {"versioned_ensembl_gene_id":"ENSG00000085514.15","gene_symbol":"PILRA","gene_name":"paired immunoglobin like type 2 receptor alpha [Source:HGNC Symbol;Acc:HGNC:20396]","synonyms":"FDF03","biotype":"protein_coding","ncbi_id":"29992","summary":"Cell signaling pathways rely on a dynamic interaction between activating and inhibiting processes. SHP-1-mediated dephosphorylation of protein tyrosine residues is central to the regulation of several cell signaling pathways. Two types of inhibitory receptor superfamily members are immunoreceptor tyrosine-based inhibitory motif (ITIM)-bearing receptors and their non-ITIM-bearing, activating counterparts. Control of cell signaling via SHP-1 is thought to occur through a balance between PILRalpha-mediated inhibition and PILRbeta-mediated activation. These paired immunoglobulin-like receptor genes are located in a tandem head-to-tail orientation on chromosome 7. This particular gene encodes the ITIM-bearing member of the receptor pair, which functions in the inhibitory role. Alternative splicing has been observed at this locus and three variants, each encoding a distinct isoform, are described. [provided by RefSeq, Jul 2008]","start":100367530,"end":100400099,"strand":1,"description":"paired immunoglobin like type 2 receptor alpha [Source:HGNC Symbol;Acc:HGNC:20396]"}, {"versioned_ensembl_gene_id":"ENSG00000267990.1","gene_symbol":"AC063977.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51137970,"end":51138634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258858.1","gene_symbol":"AL583722.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104690091,"end":104691284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213654.9","gene_symbol":"GPSM3","gene_name":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]","synonyms":"G18.2,AGS4,G18,G18.1b,NG1,C6orf9,G18.1a","biotype":"protein_coding","ncbi_id":"63940","summary":null,"start":32190766,"end":32195523,"strand":-1,"description":"G protein signaling modulator 3 [Source:HGNC Symbol;Acc:HGNC:13945]"}, {"versioned_ensembl_gene_id":"ENSG00000230098.1","gene_symbol":"TCERG1L-AS1","gene_name":"TCERG1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49532]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927489","summary":null,"start":131095218,"end":131095777,"strand":1,"description":"TCERG1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49532]"}, {"versioned_ensembl_gene_id":"ENSG00000169570.9","gene_symbol":"DTWD2","gene_name":"DTW domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19334]","synonyms":"FLJ33977","biotype":"protein_coding","ncbi_id":"285605","summary":null,"start":118837322,"end":118988545,"strand":-1,"description":"DTW domain containing 2 [Source:HGNC Symbol;Acc:HGNC:19334]"}, {"versioned_ensembl_gene_id":"ENSG00000235644.1","gene_symbol":"RPL10P5","gene_name":"ribosomal protein L10 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644911","summary":null,"start":108712262,"end":108712900,"strand":-1,"description":"ribosomal protein L10 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35724]"}, {"versioned_ensembl_gene_id":"ENSG00000254974.1","gene_symbol":"AP001372.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74485580,"end":74486051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237073.1","gene_symbol":"AL162727.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113570190,"end":113590019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270696.1","gene_symbol":"AC005034.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75660462,"end":75662208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185630.18","gene_symbol":"PBX1","gene_name":"PBX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8632]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5087","summary":"This gene encodes a nuclear protein that belongs to the PBX homeobox family of transcriptional factors. Studies in mice suggest that this gene may be involved in the regulation of osteogenesis and required for skeletal patterning and programming. A chromosomal translocation, t(1;19) involving this gene and TCF3/E2A gene, is associated with pre-B-cell acute lymphoblastic leukemia. The resulting fusion protein, in which the DNA binding domain of E2A is replaced by the DNA binding domain of this protein, transforms cells by constitutively activating transcription of genes regulated by the PBX protein family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2017]","start":164555584,"end":164899296,"strand":1,"description":"PBX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8632]"}, {"versioned_ensembl_gene_id":"ENSG00000232639.4","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"dJ570F3.6,APT,LYPLA2L","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33287152,"end":33287847,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000105204.13","gene_symbol":"DYRK1B","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 1B [Source:HGNC Symbol;Acc:HGNC:3092]","synonyms":"MIRK","biotype":"protein_coding","ncbi_id":"9149","summary":"This gene encodes a member of a family of nuclear-localized protein kinases. The encoded protein participates in the regulation of the cell cycle. Expression of this gene may be altered in tumor cells, and mutations in this gene were found to cause abdominal obesity-metabolic syndrome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":39825350,"end":39834201,"strand":-1,"description":"dual specificity tyrosine phosphorylation regulated kinase 1B [Source:HGNC Symbol;Acc:HGNC:3092]"}, {"versioned_ensembl_gene_id":"ENSG00000263644.1","gene_symbol":"AC005828.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63391191,"end":63431089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184635.15","gene_symbol":"ZNF93","gene_name":"zinc finger protein 93 [Source:HGNC Symbol;Acc:HGNC:13169]","synonyms":"ZNF505,TF34,HPF34,FLJ12488","biotype":"protein_coding","ncbi_id":"81931","summary":null,"start":19900913,"end":19963464,"strand":1,"description":"zinc finger protein 93 [Source:HGNC Symbol;Acc:HGNC:13169]"}, {"versioned_ensembl_gene_id":"ENSG00000215184.2","gene_symbol":"RPS12P16","gene_name":"ribosomal protein S12 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36595]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271352","summary":null,"start":34675635,"end":34676041,"strand":-1,"description":"ribosomal protein S12 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36595]"}, {"versioned_ensembl_gene_id":"ENSG00000270933.1","gene_symbol":"AC010719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25948657,"end":25949403,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233473.2","gene_symbol":"RAD1P2","gene_name":"RAD1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49480]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129690","summary":null,"start":159081133,"end":159081795,"strand":-1,"description":"RAD1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49480]"}, {"versioned_ensembl_gene_id":"ENSG00000225719.2","gene_symbol":"NMNAT1P2","gene_name":"NMNAT1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129160","summary":null,"start":164343005,"end":164343864,"strand":1,"description":"NMNAT1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49164]"}, {"versioned_ensembl_gene_id":"ENSG00000144741.17","gene_symbol":"SLC25A26","gene_name":"solute carrier family 25 member 26 [Source:HGNC Symbol;Acc:HGNC:20661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115286","summary":"This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]","start":66133610,"end":66388116,"strand":1,"description":"solute carrier family 25 member 26 [Source:HGNC Symbol;Acc:HGNC:20661]"}, {"versioned_ensembl_gene_id":"ENSG00000134897.13","gene_symbol":"BIVM","gene_name":"basic, immunoglobulin-like variable motif containing [Source:HGNC Symbol;Acc:HGNC:16034]","synonyms":"FLJ20159","biotype":"protein_coding","ncbi_id":"54841","summary":null,"start":102799049,"end":102841535,"strand":1,"description":"basic, immunoglobulin-like variable motif containing [Source:HGNC Symbol;Acc:HGNC:16034]"}, {"versioned_ensembl_gene_id":"ENSG00000264558.1","gene_symbol":"AC015674.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47682417,"end":47682683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254447.2","gene_symbol":"OR7E11P","gene_name":"olfactory receptor family 7 subfamily E member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:8382]","synonyms":"OR7E144P,OR11-2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10822","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":67735599,"end":67749003,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:8382]"}, {"versioned_ensembl_gene_id":"ENSG00000239412.1","gene_symbol":"RPL21P71","gene_name":"ribosomal protein L21 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:36049]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729962","summary":null,"start":147276768,"end":147277252,"strand":1,"description":"ribosomal protein L21 pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:36049]"}, {"versioned_ensembl_gene_id":"ENSG00000198252.11","gene_symbol":"STYX","gene_name":"serine/threonine/tyrosine interacting protein [Source:HGNC Symbol;Acc:HGNC:11447]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6815","summary":"The protein encoded by this gene is a pseudophosphatase, able to bind potential substrates but lacking an active catalytic loop. The encoded protein may be involved in spermiogenesis. Two transcript variants encoding the same protein have been found for these genes. [provided by RefSeq, Oct 2011]","start":52730180,"end":52774998,"strand":1,"description":"serine/threonine/tyrosine interacting protein [Source:HGNC Symbol;Acc:HGNC:11447]"}, {"versioned_ensembl_gene_id":"ENSG00000065883.14","gene_symbol":"CDK13","gene_name":"cyclin dependent kinase 13 [Source:HGNC Symbol;Acc:HGNC:1733]","synonyms":"CDC2L5,CDC2L,KIAA1791,CHED","biotype":"protein_coding","ncbi_id":"8621","summary":"The protein encoded by this gene is a member of the cyclin-dependent serine/threonine protein kinase family. Members of this family are well known for their essential roles as master switches in cell cycle control. The exact function of this protein has not yet been determined, but it may play a role in mRNA processing and may be involved in regulation of hematopoiesis. Alternatively spliced transcript variants have been described.[provided by RefSeq, Dec 2009]","start":39950037,"end":40097134,"strand":1,"description":"cyclin dependent kinase 13 [Source:HGNC Symbol;Acc:HGNC:1733]"}, {"versioned_ensembl_gene_id":"ENSG00000236032.3","gene_symbol":"OR5H14","gene_name":"olfactory receptor family 5 subfamily H member 14 [Source:HGNC Symbol;Acc:HGNC:31286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"403273","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":98147479,"end":98156614,"strand":1,"description":"olfactory receptor family 5 subfamily H member 14 [Source:HGNC Symbol;Acc:HGNC:31286]"}, {"versioned_ensembl_gene_id":"ENSG00000113272.13","gene_symbol":"THG1L","gene_name":"tRNA-histidine guanylyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:26053]","synonyms":"IHG-1,ICF45,hTHG1,FLJ20546,FLJ11601","biotype":"protein_coding","ncbi_id":"54974","summary":"The protein encoded by this gene is a mitochondrial protein that is induced by high levels of glucose and is associated with diabetic nephropathy. The encoded protein appears to increase mitochondrial biogenesis, which could lead to renal fibrosis. Another function of this protein is that of a guanyltransferase, adding GMP to the 5' end of tRNA(His). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":157731197,"end":157741448,"strand":1,"description":"tRNA-histidine guanylyltransferase 1 like [Source:HGNC Symbol;Acc:HGNC:26053]"}, {"versioned_ensembl_gene_id":"ENSG00000125482.12","gene_symbol":"TTF1","gene_name":"transcription termination factor 1 [Source:HGNC Symbol;Acc:HGNC:12397]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7270","summary":"This gene encodes a transcription termination factor that is localized to the nucleolus and plays a critical role in ribosomal gene transcription. The encoded protein mediates the termination of RNA polymerase I transcription by binding to Sal box terminator elements downstream of pre-rRNA coding regions. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. This gene shares the symbol/alias 'TFF1' with another gene, NK2 homeobox 1, also known as thyroid transcription factor 1, which plays a role in the regulation of thyroid-specific gene expression. [provided by RefSeq, Apr 2011]","start":132375548,"end":132406851,"strand":-1,"description":"transcription termination factor 1 [Source:HGNC Symbol;Acc:HGNC:12397]"}, {"versioned_ensembl_gene_id":"ENSG00000120438.11","gene_symbol":"TCP1","gene_name":"t-complex 1 [Source:HGNC Symbol;Acc:HGNC:11655]","synonyms":"D6S230E,Ccta,CCT1","biotype":"protein_coding","ncbi_id":"6950","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternate transcriptional splice variants of this gene, encoding different isoforms, have been characterized. In addition, three pseudogenes that appear to be derived from this gene have been found. [provided by RefSeq, Jun 2010]","start":159778498,"end":159789749,"strand":-1,"description":"t-complex 1 [Source:HGNC Symbol;Acc:HGNC:11655]"}, {"versioned_ensembl_gene_id":"ENSG00000115548.16","gene_symbol":"KDM3A","gene_name":"lysine demethylase 3A [Source:HGNC Symbol;Acc:HGNC:20815]","synonyms":"TSGA,KIAA0742,JMJD1A,JMJD1,JHMD2A","biotype":"protein_coding","ncbi_id":"55818","summary":"This gene encodes a zinc finger protein that contains a jumonji domain and may play a role in hormone-dependent transcriptional activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":86440647,"end":86492716,"strand":1,"description":"lysine demethylase 3A [Source:HGNC Symbol;Acc:HGNC:20815]"}, {"versioned_ensembl_gene_id":"ENSG00000236285.1","gene_symbol":"NPM1P8","gene_name":"nucleophosmin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:7928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130233","summary":null,"start":32205902,"end":32206738,"strand":1,"description":"nucleophosmin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:7928]"}, {"versioned_ensembl_gene_id":"ENSG00000266340.1","gene_symbol":"AC138207.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30978610,"end":30980250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148795.6","gene_symbol":"CYP17A1","gene_name":"cytochrome P450 family 17 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2593]","synonyms":"CYP17,CPT7,S17AH,P450C17","biotype":"protein_coding","ncbi_id":"1586","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum. It has both 17alpha-hydroxylase and 17,20-lyase activities and is a key enzyme in the steroidogenic pathway that produces progestins, mineralocorticoids, glucocorticoids, androgens, and estrogens. Mutations in this gene are associated with isolated steroid-17 alpha-hydroxylase deficiency, 17-alpha-hydroxylase/17,20-lyase deficiency, pseudohermaphroditism, and adrenal hyperplasia. [provided by RefSeq, Jul 2008]","start":102830531,"end":102837533,"strand":-1,"description":"cytochrome P450 family 17 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2593]"}, {"versioned_ensembl_gene_id":"ENSG00000234838.3","gene_symbol":"AC092373.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66572057,"end":66572546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270033.1","gene_symbol":"AC053481.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":62272487,"end":62282915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269519.1","gene_symbol":"AC005176.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39631300,"end":39631446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167757.13","gene_symbol":"KLK11","gene_name":"kallikrein related peptidase 11 [Source:HGNC Symbol;Acc:HGNC:6359]","synonyms":"TLSP,PRSS20","biotype":"protein_coding","ncbi_id":"11012","summary":"Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Alternate splicing and the use of alternate promoters results in multiple transcript variants encoding distinct isoforms which are differentially expressed. [provided by RefSeq, Dec 2016]","start":51022216,"end":51028039,"strand":-1,"description":"kallikrein related peptidase 11 [Source:HGNC Symbol;Acc:HGNC:6359]"}, {"versioned_ensembl_gene_id":"ENSG00000231561.2","gene_symbol":"CEACAMP5","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1827]","synonyms":"CGM12","biotype":"unprocessed_pseudogene","ncbi_id":"1085","summary":null,"start":42654200,"end":42669076,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1827]"}, {"versioned_ensembl_gene_id":"ENSG00000232327.4","gene_symbol":"AC105917.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80386178,"end":80388716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258589.6","gene_symbol":"CR753842.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31648058,"end":31654629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233210.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"ANKRD59,D6S54E,GPATCH10,BAT4,G5","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31643407,"end":31648462,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000284615.1","gene_symbol":"AL078582.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":152112759,"end":152118397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072182.12","gene_symbol":"ASIC4","gene_name":"acid sensing ion channel subunit family member 4 [Source:HGNC Symbol;Acc:HGNC:21263]","synonyms":"BNAC4,ACCN4","biotype":"protein_coding","ncbi_id":"55515","summary":"This gene belongs to the superfamily of acid-sensing ion channels, which are proton-gated, amiloride-sensitive sodium channels. These channels have been implicated in synaptic transmission, pain perception as well as mechanoperception. This gene is predominantly expressed in the pituitary gland, and was considered a candidate for paroxysmal dystonic choreoathetosis (PDC), a movement disorder, however, no correlation was found between mutations in this gene and PDC. [provided by RefSeq, Feb 2012]","start":219514170,"end":219538772,"strand":1,"description":"acid sensing ion channel subunit family member 4 [Source:HGNC Symbol;Acc:HGNC:21263]"}, {"versioned_ensembl_gene_id":"ENSG00000231178.1","gene_symbol":"AL357832.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159353922,"end":159354673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244672.4","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31652558,"end":31655955,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000246528.3","gene_symbol":"AC079089.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69834111,"end":69854971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105088.8","gene_symbol":"OLFM2","gene_name":"olfactomedin 2 [Source:HGNC Symbol;Acc:HGNC:17189]","synonyms":"OlfC,NOE2","biotype":"protein_coding","ncbi_id":"93145","summary":null,"start":9853718,"end":9936552,"strand":-1,"description":"olfactomedin 2 [Source:HGNC Symbol;Acc:HGNC:17189]"}, {"versioned_ensembl_gene_id":"ENSG00000277299.1","gene_symbol":"AC084876.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109948389,"end":109949029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139437.17","gene_symbol":"TCHP","gene_name":"trichoplein keratin filament binding [Source:HGNC Symbol;Acc:HGNC:28135]","synonyms":"TpMs,MGC10854","biotype":"protein_coding","ncbi_id":"84260","summary":null,"start":109900264,"end":109983841,"strand":1,"description":"trichoplein keratin filament binding [Source:HGNC Symbol;Acc:HGNC:28135]"}, {"versioned_ensembl_gene_id":"ENSG00000268739.1","gene_symbol":"AC011473.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51014374,"end":51014734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137571.10","gene_symbol":"SLCO5A1","gene_name":"solute carrier organic anion transporter family member 5A1 [Source:HGNC Symbol;Acc:HGNC:19046]","synonyms":"OATP-J,SLC21A15,OATPRP4,OATP5A1","biotype":"protein_coding","ncbi_id":"81796","summary":"This gene encodes a 12 transmembrane domain protein that is a member of the solute carrier organic anion transporter superfamily. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":69667047,"end":69835064,"strand":-1,"description":"solute carrier organic anion transporter family member 5A1 [Source:HGNC Symbol;Acc:HGNC:19046]"}, {"versioned_ensembl_gene_id":"ENSG00000271113.1","gene_symbol":"AC079089.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69794062,"end":69794734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254624.1","gene_symbol":"OR4R3P","gene_name":"olfactory receptor family 4 subfamily R member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15182]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81298","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49923049,"end":49923886,"strand":1,"description":"olfactory receptor family 4 subfamily R member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15182]"}, {"versioned_ensembl_gene_id":"ENSG00000226850.2","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"NG38,ATP6G,Em:AC004181.3,Vma10,ATP6G2","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31583922,"end":31586304,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000110422.11","gene_symbol":"HIPK3","gene_name":"homeodomain interacting protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:4915]","synonyms":"YAK1,PKY,FIST3,DYRK6","biotype":"protein_coding","ncbi_id":"10114","summary":null,"start":33256672,"end":33357023,"strand":1,"description":"homeodomain interacting protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:4915]"}, {"versioned_ensembl_gene_id":"ENSG00000149418.10","gene_symbol":"ST14","gene_name":"suppression of tumorigenicity 14 [Source:HGNC Symbol;Acc:HGNC:11344]","synonyms":"TMPRSS14,SNC19,PRSS14,MT-SP1,HAI","biotype":"protein_coding","ncbi_id":"6768","summary":"The protein encoded by this gene is an epithelial-derived, integral membrane serine protease. This protease forms a complex with the Kunitz-type serine protease inhibitor, HAI-1, and is found to be activated by sphingosine 1-phosphate. This protease has been shown to cleave and activate hepatocyte growth factor/scattering factor, and urokinase plasminogen activator, which suggest the function of this protease as an epithelial membrane activator for other proteases and latent growth factors. The expression of this protease has been associated with breast, colon, prostate, and ovarian tumors, which implicates its role in cancer invasion, and metastasis. [provided by RefSeq, Jul 2008]","start":130159562,"end":130210376,"strand":1,"description":"suppression of tumorigenicity 14 [Source:HGNC Symbol;Acc:HGNC:11344]"}, {"versioned_ensembl_gene_id":"ENSG00000138381.9","gene_symbol":"ASNSD1","gene_name":"asparagine synthetase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24910]","synonyms":"NS3TP1,NBLA00058,FLJ20752","biotype":"protein_coding","ncbi_id":"54529","summary":null,"start":189661385,"end":189670831,"strand":1,"description":"asparagine synthetase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24910]"}, {"versioned_ensembl_gene_id":"ENSG00000241135.5","gene_symbol":"LINC00881","gene_name":"long intergenic non-protein coding RNA 881 [Source:HGNC Symbol;Acc:HGNC:48567]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100498859","summary":null,"start":157089881,"end":157101135,"strand":1,"description":"long intergenic non-protein coding RNA 881 [Source:HGNC Symbol;Acc:HGNC:48567]"}, {"versioned_ensembl_gene_id":"ENSG00000249031.1","gene_symbol":"SUMO2P6","gene_name":"SUMO2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127922","summary":null,"start":174561776,"end":174562063,"strand":1,"description":"SUMO2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39016]"}, {"versioned_ensembl_gene_id":"ENSG00000156711.16","gene_symbol":"MAPK13","gene_name":"mitogen-activated protein kinase 13 [Source:HGNC Symbol;Acc:HGNC:6875]","synonyms":"p38delta,SAPK4,PRKM13","biotype":"protein_coding","ncbi_id":"5603","summary":"This gene encodes a member of the mitogen-activated protein (MAP) kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. The encoded protein is a p38 MAP kinase and is activated by proinflammatory cytokines and cellular stress. Substrates of the encoded protein include the transcription factor ATF2 and the microtubule dynamics regulator stathmin. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":36127809,"end":36144524,"strand":1,"description":"mitogen-activated protein kinase 13 [Source:HGNC Symbol;Acc:HGNC:6875]"}, {"versioned_ensembl_gene_id":"ENSG00000251596.1","gene_symbol":"HADHAP1","gene_name":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4802]","synonyms":"HADHAP","biotype":"processed_pseudogene","ncbi_id":"3031","summary":null,"start":165404067,"end":165406350,"strand":-1,"description":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4802]"}, {"versioned_ensembl_gene_id":"ENSG00000143819.12","gene_symbol":"EPHX1","gene_name":"epoxide hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3401]","synonyms":"EPHX","biotype":"protein_coding","ncbi_id":"2052","summary":"Epoxide hydrolase is a critical biotransformation enzyme that converts epoxides from the degradation of aromatic compounds to trans-dihydrodiols which can be conjugated and excreted from the body. Epoxide hydrolase functions in both the activation and detoxification of epoxides. Mutations in this gene cause preeclampsia, epoxide hydrolase deficiency or increased epoxide hydrolase activity. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2008]","start":225810092,"end":225845563,"strand":1,"description":"epoxide hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3401]"}, {"versioned_ensembl_gene_id":"ENSG00000145632.14","gene_symbol":"PLK2","gene_name":"polo like kinase 2 [Source:HGNC Symbol;Acc:HGNC:19699]","synonyms":"SNK","biotype":"protein_coding","ncbi_id":"10769","summary":"The protein encoded by this gene is a member of the polo family of serine/threonine protein kinases that have a role in normal cell division. This gene is most abundantly expressed in testis, spleen and fetal tissues, and its expression is inducible by serum, suggesting that it may also play an important role in cells undergoing rapid cell division. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":58453982,"end":58460260,"strand":-1,"description":"polo like kinase 2 [Source:HGNC Symbol;Acc:HGNC:19699]"}, {"versioned_ensembl_gene_id":"ENSG00000276698.1","gene_symbol":"AL136295.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24198433,"end":24199090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259522.3","gene_symbol":"AL136295.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24180395,"end":24190416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173349.5","gene_symbol":"SFT2D3","gene_name":"SFT2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28767]","synonyms":"MGC5391","biotype":"protein_coding","ncbi_id":"84826","summary":null,"start":127701508,"end":127705242,"strand":1,"description":"SFT2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28767]"}, {"versioned_ensembl_gene_id":"ENSG00000255960.1","gene_symbol":"AC092851.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18424663,"end":18425140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167971.15","gene_symbol":"CASKIN1","gene_name":"CASK interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20879]","synonyms":"KIAA1306,ANKS5A","biotype":"protein_coding","ncbi_id":"57524","summary":null,"start":2177180,"end":2196525,"strand":-1,"description":"CASK interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20879]"}, {"versioned_ensembl_gene_id":"ENSG00000256708.1","gene_symbol":"AC007458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68143318,"end":68143690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233435.2","gene_symbol":"AGGF1P2","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644435","summary":null,"start":133640789,"end":133642894,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38052]"}, {"versioned_ensembl_gene_id":"ENSG00000213543.2","gene_symbol":"RARRES2P2","gene_name":"retinoic acid receptor responder 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48701]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644425","summary":null,"start":133637408,"end":133637892,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48701]"}, {"versioned_ensembl_gene_id":"ENSG00000184156.16","gene_symbol":"KCNQ3","gene_name":"potassium voltage-gated channel subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:6297]","synonyms":"EBN2,Kv7.3","biotype":"protein_coding","ncbi_id":"3786","summary":"This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]","start":132120858,"end":132481019,"strand":-1,"description":"potassium voltage-gated channel subfamily Q member 3 [Source:HGNC Symbol;Acc:HGNC:6297]"}, {"versioned_ensembl_gene_id":"ENSG00000254268.1","gene_symbol":"RFPL4AP7","gene_name":"ret finger protein like 4A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45143]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420055","summary":null,"start":49352630,"end":49352844,"strand":-1,"description":"ret finger protein like 4A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:45143]"}, {"versioned_ensembl_gene_id":"ENSG00000269903.1","gene_symbol":"AC025165.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57814494,"end":57814926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163565.18","gene_symbol":"IFI16","gene_name":"interferon gamma inducible protein 16 [Source:HGNC Symbol;Acc:HGNC:5395]","synonyms":"PYHIN2,IFNGIP1","biotype":"protein_coding","ncbi_id":"3428","summary":"This gene encodes a member of the HIN-200 (hematopoietic interferon-inducible nuclear antigens with 200 amino acid repeats) family of cytokines. The encoded protein contains domains involved in DNA binding, transcriptional regulation, and protein-protein interactions. The protein localizes to the nucleoplasm and nucleoli, and interacts with p53 and retinoblastoma-1. It modulates p53 function, and inhibits cell growth in the Ras/Raf signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2011]","start":158999968,"end":159055155,"strand":1,"description":"interferon gamma inducible protein 16 [Source:HGNC Symbol;Acc:HGNC:5395]"}, {"versioned_ensembl_gene_id":"ENSG00000204779.2","gene_symbol":"FOXD4L5","gene_name":"forkhead box D4 like 5 [Source:HGNC Symbol;Acc:HGNC:18522]","synonyms":"OTTHUMG00000013332,bA15J10.2","biotype":"protein_coding","ncbi_id":"653427","summary":null,"start":65282101,"end":65285209,"strand":-1,"description":"forkhead box D4 like 5 [Source:HGNC Symbol;Acc:HGNC:18522]"}, {"versioned_ensembl_gene_id":"ENSG00000230711.2","gene_symbol":"CTAGE13P","gene_name":"CTAGE family member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:37298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421638","summary":null,"start":168286905,"end":168289350,"strand":-1,"description":"CTAGE family member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:37298]"}, {"versioned_ensembl_gene_id":"ENSG00000229751.1","gene_symbol":"AC044781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13991815,"end":14007526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225112.1","gene_symbol":"AL157392.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13710415,"end":13712054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276828.1","gene_symbol":"AC012488.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":189625443,"end":189626259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265973.1","gene_symbol":"AP006587.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49843488,"end":49846533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264177.1","gene_symbol":"AL353997.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18379855,"end":18388984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134812.7","gene_symbol":"GIF","gene_name":"gastric intrinsic factor [Source:HGNC Symbol;Acc:HGNC:4268]","synonyms":"TCN3,INF,IFMH,IF","biotype":"protein_coding","ncbi_id":"2694","summary":"This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia. [provided by RefSeq, Jul 2008]","start":59829268,"end":59845501,"strand":-1,"description":"gastric intrinsic factor [Source:HGNC Symbol;Acc:HGNC:4268]"}, {"versioned_ensembl_gene_id":"ENSG00000163515.6","gene_symbol":"RETNLB","gene_name":"resistin like beta [Source:HGNC Symbol;Acc:HGNC:20388]","synonyms":"HXCP2,FIZZ2,RELMb","biotype":"protein_coding","ncbi_id":"84666","summary":null,"start":108743424,"end":108757384,"strand":-1,"description":"resistin like beta [Source:HGNC Symbol;Acc:HGNC:20388]"}, {"versioned_ensembl_gene_id":"ENSG00000231181.1","gene_symbol":"AL954705.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9576427,"end":9576985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185245.7","gene_symbol":"GP1BA","gene_name":"glycoprotein Ib platelet alpha subunit [Source:HGNC Symbol;Acc:HGNC:4439]","synonyms":"GPIbalpha,GP1B,CD42b","biotype":"protein_coding","ncbi_id":"2811","summary":"Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that is linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease. The coding region of this gene is known to contain a polymophic variable number tandem repeat (VNTR) domain that is associated with susceptibility to nonarteritic anterior ischemic optic neuropathy. [provided by RefSeq, Oct 2013]","start":4932297,"end":4935030,"strand":1,"description":"glycoprotein Ib platelet alpha subunit [Source:HGNC Symbol;Acc:HGNC:4439]"}, {"versioned_ensembl_gene_id":"ENSG00000269713.7","gene_symbol":"NBPF9","gene_name":"NBPF member 9 [Source:HGNC Symbol;Acc:HGNC:31991]","synonyms":"AE01","biotype":"protein_coding","ncbi_id":"400818","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2013]","start":149054027,"end":149103561,"strand":-1,"description":"NBPF member 9 [Source:HGNC Symbol;Acc:HGNC:31991]"}, {"versioned_ensembl_gene_id":"ENSG00000162458.12","gene_symbol":"FBLIM1","gene_name":"filamin binding LIM protein 1 [Source:HGNC Symbol;Acc:HGNC:24686]","synonyms":"migfilin,FBLP-1,CAL","biotype":"protein_coding","ncbi_id":"54751","summary":"This gene encodes a protein with an N-terminal filamin-binding domain, a central proline-rich domain, and, multiple C-terminal LIM domains. This protein localizes at cell junctions and may link cell adhesion structures to the actin cytoskeleton. This protein may be involved in the assembly and stabilization of actin-filaments and likely plays a role in modulating cell adhesion, cell morphology and cell motility. This protein also localizes to the nucleus and may affect cardiomyocyte differentiation after binding with the CSX/NKX2-5 transcription factor. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":15756607,"end":15786594,"strand":1,"description":"filamin binding LIM protein 1 [Source:HGNC Symbol;Acc:HGNC:24686]"}, {"versioned_ensembl_gene_id":"ENSG00000255772.5","gene_symbol":"LINC01479","gene_name":"long intergenic non-protein coding RNA 1479 [Source:HGNC Symbol;Acc:HGNC:51123]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927922","summary":null,"start":67929235,"end":67970017,"strand":1,"description":"long intergenic non-protein coding RNA 1479 [Source:HGNC Symbol;Acc:HGNC:51123]"}, {"versioned_ensembl_gene_id":"ENSG00000235717.1","gene_symbol":"DPP10-AS2","gene_name":"DPP10 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40940]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478969","summary":null,"start":114833830,"end":114835588,"strand":-1,"description":"DPP10 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40940]"}, {"versioned_ensembl_gene_id":"ENSG00000143742.12","gene_symbol":"SRP9","gene_name":"signal recognition particle 9 [Source:HGNC Symbol;Acc:HGNC:11304]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6726","summary":null,"start":225777813,"end":225790466,"strand":1,"description":"signal recognition particle 9 [Source:HGNC Symbol;Acc:HGNC:11304]"}, {"versioned_ensembl_gene_id":"ENSG00000266162.1","gene_symbol":"YWHAEP2","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49429]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481688","summary":null,"start":18418195,"end":18418306,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49429]"}, {"versioned_ensembl_gene_id":"ENSG00000066117.14","gene_symbol":"SMARCD1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 [Source:HGNC Symbol;Acc:HGNC:11106]","synonyms":"Rsc6p,CRACD1,BAF60A","biotype":"protein_coding","ncbi_id":"6602","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":50084972,"end":50100712,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 [Source:HGNC Symbol;Acc:HGNC:11106]"}, {"versioned_ensembl_gene_id":"ENSG00000225201.6","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30567930,"end":30572668,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000224648.1","gene_symbol":"LINC01627","gene_name":"long intergenic non-protein coding RNA 1627 [Source:HGNC Symbol;Acc:HGNC:52258]","synonyms":"RP11-397D12.4","biotype":"lincRNA","ncbi_id":"105376036","summary":null,"start":37383178,"end":37384434,"strand":-1,"description":"long intergenic non-protein coding RNA 1627 [Source:HGNC Symbol;Acc:HGNC:52258]"}, {"versioned_ensembl_gene_id":"ENSG00000238094.1","gene_symbol":"AC245036.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54607870,"end":54608376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256804.1","gene_symbol":"AC138466.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132126461,"end":132126764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235129.1","gene_symbol":"FABP7P2","gene_name":"fatty acid binding protein 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41952]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874317","summary":null,"start":95368507,"end":95368885,"strand":-1,"description":"fatty acid binding protein 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41952]"}, {"versioned_ensembl_gene_id":"ENSG00000198049.6","gene_symbol":"AVPR1B","gene_name":"arginine vasopressin receptor 1B [Source:HGNC Symbol;Acc:HGNC:896]","synonyms":"AVPR3","biotype":"protein_coding","ncbi_id":"553","summary":"The protein encoded by this gene acts as receptor for arginine vasopressin. This receptor belongs to the subfamily of G-protein coupled receptors which includes AVPR1A, V2R and OXT receptors. Its activity is mediated by G proteins which stimulate a phosphatidylinositol-calcium second messenger system. The receptor is primarily located in the anterior pituitary, where it stimulates ACTH release. It is expressed at high levels in ACTH-secreting pituitary adenomas as well as in bronchial carcinoids responsible for the ectopic ACTH syndrome. A spliced antisense transcript of this gene has been reported but its function is not known. [provided by RefSeq, Jul 2008]","start":206109692,"end":206117699,"strand":-1,"description":"arginine vasopressin receptor 1B [Source:HGNC Symbol;Acc:HGNC:896]"}, {"versioned_ensembl_gene_id":"ENSG00000248109.2","gene_symbol":"AC011346.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":148221650,"end":148243580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271115.1","gene_symbol":"AC010738.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57048350,"end":57049336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084676.15","gene_symbol":"NCOA1","gene_name":"nuclear receptor coactivator 1 [Source:HGNC Symbol;Acc:HGNC:7668]","synonyms":"SRC1,RIP160,NCoA-1,KAT13A,F-SRC-1,bHLHe74","biotype":"protein_coding","ncbi_id":"8648","summary":"The protein encoded by this gene acts as a transcriptional coactivator for steroid and nuclear hormone receptors. It is a member of the p160/steroid receptor coactivator (SRC) family and like other family members has histone acetyltransferase activity and contains a nuclear localization signal, as well as bHLH and PAS domains. The product of this gene binds nuclear receptors directly and stimulates the transcriptional activities in a hormone-dependent fashion. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":24491914,"end":24770702,"strand":1,"description":"nuclear receptor coactivator 1 [Source:HGNC Symbol;Acc:HGNC:7668]"}, {"versioned_ensembl_gene_id":"ENSG00000274855.1","gene_symbol":"AL133351.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3033183,"end":3033288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228725.3","gene_symbol":"MTND2P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42113]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873344","summary":null,"start":19603797,"end":19605048,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42113]"}, {"versioned_ensembl_gene_id":"ENSG00000259195.1","gene_symbol":"AC021739.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85770990,"end":85771163,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197550.3","gene_symbol":"AL359955.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64817870,"end":64836341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213235.3","gene_symbol":"EEF1A1P16","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387845","summary":null,"start":16990670,"end":16992083,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:37889]"}, {"versioned_ensembl_gene_id":"ENSG00000161203.13","gene_symbol":"AP2M1","gene_name":"adaptor related protein complex 2 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:564]","synonyms":"mu2,CLAPM1,AP50","biotype":"protein_coding","ncbi_id":"1173","summary":"This gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar ATPase, which is responsible for proton pumping occurring in the acidification of endosomes and lysosomes. The encoded protein may also play an important role in regulating the intracellular trafficking and function of CTLA-4 protein. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":184174689,"end":184184091,"strand":1,"description":"adaptor related protein complex 2 mu 1 subunit [Source:HGNC Symbol;Acc:HGNC:564]"}, {"versioned_ensembl_gene_id":"ENSG00000232260.2","gene_symbol":"BTF3L4P1","gene_name":"basic transcription factor 3 like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39645]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505945","summary":null,"start":17518526,"end":17518993,"strand":-1,"description":"basic transcription factor 3 like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39645]"}, {"versioned_ensembl_gene_id":"ENSG00000279349.1","gene_symbol":"AC092692.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":112525548,"end":112528142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244020.2","gene_symbol":"MT1HL1","gene_name":"metallothionein 1H like 1 [Source:HGNC Symbol;Acc:HGNC:31864]","synonyms":"MT1P2","biotype":"protein_coding","ncbi_id":"645745","summary":"This gene is a retrotransposed gene, compared to MT1H (GeneID:4496). This retrogene is transcribed. It retains a full-length CDS, and is assumed to be translated. Compared to the MT1H product, this protein product differs at three internal amino acids, two of which are at metal-binding sites. [provided by RefSeq, Mar 2013]","start":237004103,"end":237004418,"strand":-1,"description":"metallothionein 1H like 1 [Source:HGNC Symbol;Acc:HGNC:31864]"}, {"versioned_ensembl_gene_id":"ENSG00000251432.6","gene_symbol":"AC108062.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128292751,"end":128519394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224167.1","gene_symbol":"AL390729.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112850028,"end":112877871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259241.1","gene_symbol":"AC020892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51693216,"end":51695765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186049.8","gene_symbol":"KRT73","gene_name":"keratin 73 [Source:HGNC Symbol;Acc:HGNC:28928]","synonyms":"KRT6IRS3,K6IRS3","biotype":"protein_coding","ncbi_id":"319101","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes a protein that is expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]","start":52607570,"end":52618559,"strand":-1,"description":"keratin 73 [Source:HGNC Symbol;Acc:HGNC:28928]"}, {"versioned_ensembl_gene_id":"ENSG00000261595.1","gene_symbol":"AL603832.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112715672,"end":112717796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134247.9","gene_symbol":"PTGFRN","gene_name":"prostaglandin F2 receptor inhibitor [Source:HGNC Symbol;Acc:HGNC:9601]","synonyms":"SMAP-6,KIAA1436,FPRP,FLJ11001,EWI-F,CD9P-1,CD315","biotype":"protein_coding","ncbi_id":"5738","summary":null,"start":116910057,"end":116990358,"strand":1,"description":"prostaglandin F2 receptor inhibitor [Source:HGNC Symbol;Acc:HGNC:9601]"}, {"versioned_ensembl_gene_id":"ENSG00000232098.3","gene_symbol":"AC012313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58404238,"end":58408484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272715.1","gene_symbol":"AL157904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116909149,"end":116909531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237595.3","gene_symbol":"AL161937.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50162765,"end":50166102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143248.12","gene_symbol":"RGS5","gene_name":"regulator of G protein signaling 5 [Source:HGNC Symbol;Acc:HGNC:10001]","synonyms":"MSTP106,MSTP092,MSTP032,MST129,MST106,MST092,MSTP129","biotype":"protein_coding","ncbi_id":"8490","summary":"This gene encodes a member of the regulators of G protein signaling (RGS) family. The RGS proteins are signal transduction molecules which are involved in the regulation of heterotrimeric G proteins by acting as GTPase activators. This gene is a hypoxia-inducible factor-1 dependent, hypoxia-induced gene which is involved in the induction of endothelial apoptosis. This gene is also one of three genes on chromosome 1q contributing to elevated blood pressure. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Dec 2011]","start":163111121,"end":163321791,"strand":-1,"description":"regulator of G protein signaling 5 [Source:HGNC Symbol;Acc:HGNC:10001]"}, {"versioned_ensembl_gene_id":"ENSG00000116783.14","gene_symbol":"TNNI3K","gene_name":"TNNI3 interacting kinase [Source:HGNC Symbol;Acc:HGNC:19661]","synonyms":"CARK","biotype":"protein_coding","ncbi_id":"51086","summary":"This gene encodes a protein that belongs to the MAP kinase kinase kinase (MAPKKK) family of protein kinases. The protein contains ankyrin repeat, protein kinase and serine-rich domains and is thought to play a role in cardiac physiology. [provided by RefSeq, Sep 2012]","start":74235401,"end":74544428,"strand":1,"description":"TNNI3 interacting kinase [Source:HGNC Symbol;Acc:HGNC:19661]"}, {"versioned_ensembl_gene_id":"ENSG00000235088.1","gene_symbol":"AL031667.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41459354,"end":41461944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220181.1","gene_symbol":"AL357075.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154549517,"end":154550242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226412.1","gene_symbol":"AC018980.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33578931,"end":33600040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234557.2","gene_symbol":"AL035422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101443707,"end":101444103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233894.1","gene_symbol":"AC105271.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74468195,"end":74469543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184381.18","gene_symbol":"PLA2G6","gene_name":"phospholipase A2 group VI [Source:HGNC Symbol;Acc:HGNC:9039]","synonyms":"PNPLA9,PARK14,NBIA2,iPLA2beta,iPLA2","biotype":"protein_coding","ncbi_id":"8398","summary":"The protein encoded by this gene is an A2 phospholipase, a class of enzyme that catalyzes the release of fatty acids from phospholipids. The encoded protein may play a role in phospholipid remodelling, arachidonic acid release, leukotriene and prostaglandin synthesis, fas-mediated apoptosis, and transmembrane ion flux in glucose-stimulated B-cells. Several transcript variants encoding multiple isoforms have been described, but the full-length nature of only three of them have been determined to date. [provided by RefSeq, Dec 2010]","start":38111495,"end":38205690,"strand":-1,"description":"phospholipase A2 group VI [Source:HGNC Symbol;Acc:HGNC:9039]"}, {"versioned_ensembl_gene_id":"ENSG00000255532.1","gene_symbol":"AC118942.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49305714,"end":49379669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233469.1","gene_symbol":"ST6GALNAC4P1","gene_name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874524","summary":null,"start":19818121,"end":19818619,"strand":-1,"description":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39660]"}, {"versioned_ensembl_gene_id":"ENSG00000116176.6","gene_symbol":"TPSG1","gene_name":"tryptase gamma 1 [Source:HGNC Symbol;Acc:HGNC:14134]","synonyms":"TMT,PRSS31","biotype":"protein_coding","ncbi_id":"25823","summary":"Tryptases comprise a family of trypsin-like serine proteases, the peptidase family S1. Tryptases are enzymatically active only as heparin-stabilized tetramers, and they are resistant to all known endogenous proteinase inhibitors. Several tryptase genes are clustered on chromosome 16p13.3. There is uncertainty regarding the number of genes in this cluster. Currently four functional genes - alpha I, beta I, beta II and gamma I - have been identified. And beta I has an allelic variant named alpha II, beta II has an allelic variant beta III, also gamma I has an allelic variant gamma II. Beta tryptases appear to be the main isoenzymes expressed in mast cells; whereas in basophils, alpha-tryptases predominant. This gene differs from other members of the tryptase gene family in that it has C-terminal hydrophobic domain, which may serve as a membrane anchor. Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders. [provided by RefSeq, Jul 2008]","start":1221651,"end":1225257,"strand":-1,"description":"tryptase gamma 1 [Source:HGNC Symbol;Acc:HGNC:14134]"}, {"versioned_ensembl_gene_id":"ENSG00000264695.1","gene_symbol":"AC007922.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24489375,"end":24491080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152240.12","gene_symbol":"HAUS1","gene_name":"HAUS augmin like complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:25174]","synonyms":"HsT1461,HEI-C,FLJ40084,CCDC5","biotype":"protein_coding","ncbi_id":"115106","summary":"HAUS1 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]","start":46104332,"end":46128333,"strand":1,"description":"HAUS augmin like complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:25174]"}, {"versioned_ensembl_gene_id":"ENSG00000233369.7","gene_symbol":"GTF2IP4","gene_name":"general transcription factor IIi pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51716]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100093631","summary":null,"start":73154938,"end":73207283,"strand":1,"description":"general transcription factor IIi pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51716]"}, {"versioned_ensembl_gene_id":"ENSG00000164691.16","gene_symbol":"TAGAP","gene_name":"T-cell activation RhoGTPase activating protein [Source:HGNC Symbol;Acc:HGNC:15669]","synonyms":"ARHGAP47,IDDM21,FLJ32631","biotype":"protein_coding","ncbi_id":"117289","summary":"This gene encodes a member of the Rho GTPase-activator protein superfamily. The encoded protein may function as a Rho GTPase-activating protein. Alterations in this gene may be associated with several diseases, including rheumatoid arthritis, celiac disease, and multiple sclerosis. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]","start":159034468,"end":159045152,"strand":-1,"description":"T-cell activation RhoGTPase activating protein [Source:HGNC Symbol;Acc:HGNC:15669]"}, {"versioned_ensembl_gene_id":"ENSG00000169131.11","gene_symbol":"ZNF354A","gene_name":"zinc finger protein 354A [Source:HGNC Symbol;Acc:HGNC:11628]","synonyms":"TCF17,KID1,KID-1,HKL1,EZNF","biotype":"protein_coding","ncbi_id":"6940","summary":null,"start":178694605,"end":178730702,"strand":-1,"description":"zinc finger protein 354A [Source:HGNC Symbol;Acc:HGNC:11628]"}, {"versioned_ensembl_gene_id":"ENSG00000224066.1","gene_symbol":"AL049795.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32204769,"end":32206814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282819.1","gene_symbol":"AL122127.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105786276,"end":105786602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198087.7","gene_symbol":"CD2AP","gene_name":"CD2 associated protein [Source:HGNC Symbol;Acc:HGNC:14258]","synonyms":"CMS","biotype":"protein_coding","ncbi_id":"23607","summary":"This gene encodes a scaffolding molecule that regulates the actin cytoskeleton. The protein directly interacts with filamentous actin and a variety of cell membrane proteins through multiple actin binding sites, SH3 domains, and a proline-rich region containing binding sites for SH3 domains. The cytoplasmic protein localizes to membrane ruffles, lipid rafts, and the leading edges of cells. It is implicated in dynamic actin remodeling and membrane trafficking that occurs during receptor endocytosis and cytokinesis. Haploinsufficiency of this gene is implicated in susceptibility to glomerular disease. [provided by RefSeq, Jul 2008]","start":47477789,"end":47627263,"strand":1,"description":"CD2 associated protein [Source:HGNC Symbol;Acc:HGNC:14258]"}, {"versioned_ensembl_gene_id":"ENSG00000230675.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32796644,"end":32804081,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000206488.10","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"Em:AB023049.7,MEC17,C6orf134,FLJ13158","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30616337,"end":30636318,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000248901.1","gene_symbol":"LINC01846","gene_name":"long intergenic non-protein coding RNA 1846 [Source:HGNC Symbol;Acc:HGNC:52661]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105379098","summary":null,"start":98086260,"end":98161193,"strand":-1,"description":"long intergenic non-protein coding RNA 1846 [Source:HGNC Symbol;Acc:HGNC:52661]"}, {"versioned_ensembl_gene_id":"ENSG00000160307.9","gene_symbol":"S100B","gene_name":"S100 calcium binding protein B [Source:HGNC Symbol;Acc:HGNC:10500]","synonyms":"S100beta","biotype":"protein_coding","ncbi_id":"6285","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 21q22.3. This protein may function in Neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes. [provided by RefSeq, Jul 2008]","start":46598962,"end":46605208,"strand":-1,"description":"S100 calcium binding protein B [Source:HGNC Symbol;Acc:HGNC:10500]"}, {"versioned_ensembl_gene_id":"ENSG00000213076.3","gene_symbol":"AL627422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158921271,"end":158922150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248586.2","gene_symbol":"AC025470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57317989,"end":57320020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255269.2","gene_symbol":"AC024475.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46213824,"end":46220438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250169.1","gene_symbol":"MTND5P13","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42304]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873272","summary":null,"start":64609454,"end":64610532,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:42304]"}, {"versioned_ensembl_gene_id":"ENSG00000171311.12","gene_symbol":"EXOSC1","gene_name":"exosome component 1 [Source:HGNC Symbol;Acc:HGNC:17286]","synonyms":"CSL4,CGI-108,Ski4p,SKI4,p13,hCsl4p,Csl4p","biotype":"protein_coding","ncbi_id":"51013","summary":"This gene encodes a core component of the exosome. The mammalian exosome is required for rapid degradation of AU rich element-containing RNAs but not for poly(A) shortening. The association of this protein with the exosome is mediated by protein-protein interactions with ribosomal RNA-processing protein 42 and ribosomal RNA-processing protein 46. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":97436142,"end":97446017,"strand":-1,"description":"exosome component 1 [Source:HGNC Symbol;Acc:HGNC:17286]"}, {"versioned_ensembl_gene_id":"ENSG00000227847.1","gene_symbol":"AC010099.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125345825,"end":125346197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259571.1","gene_symbol":"BLID","gene_name":"BH3-like motif containing, cell death inducer [Source:HGNC Symbol;Acc:HGNC:33495]","synonyms":"BRCC2","biotype":"protein_coding","ncbi_id":"414899","summary":"This gene encodes a BH3-like motif containing protein involved in cell death. The encoded protein may induce apoptosis in a caspase-dependent manner. The protein is localized in both the cytoplasm and the mitochondrion. [provided by RefSeq, Aug 2011]","start":122115354,"end":122116215,"strand":-1,"description":"BH3-like motif containing, cell death inducer [Source:HGNC Symbol;Acc:HGNC:33495]"}, {"versioned_ensembl_gene_id":"ENSG00000205898.3","gene_symbol":"AC019155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125159974,"end":125160547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108556.7","gene_symbol":"CHRNE","gene_name":"cholinergic receptor nicotinic epsilon subunit [Source:HGNC Symbol;Acc:HGNC:1966]","synonyms":"ACHRE","biotype":"protein_coding","ncbi_id":"1145","summary":"Acetylcholine receptors at mature mammalian neuromuscular junctions are pentameric protein complexes composed of four subunits in the ratio of two alpha subunits to one beta, one epsilon, and one delta subunit. The acetylcholine receptor changes subunit composition shortly after birth when the epsilon subunit replaces the gamma subunit seen in embryonic receptors. Mutations in the epsilon subunit are associated with congenital myasthenic syndrome. [provided by RefSeq, Sep 2009]","start":4897774,"end":4903074,"strand":-1,"description":"cholinergic receptor nicotinic epsilon subunit [Source:HGNC Symbol;Acc:HGNC:1966]"}, {"versioned_ensembl_gene_id":"ENSG00000253698.1","gene_symbol":"AC136601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178350867,"end":178352250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232920.1","gene_symbol":"LINC01400","gene_name":"long intergenic non-protein coding RNA 1400 [Source:HGNC Symbol;Acc:HGNC:50681]","synonyms":"TCONS_00015805","biotype":"lincRNA","ncbi_id":"107080554","summary":null,"start":37073531,"end":37075792,"strand":-1,"description":"long intergenic non-protein coding RNA 1400 [Source:HGNC Symbol;Acc:HGNC:50681]"}, {"versioned_ensembl_gene_id":"ENSG00000177679.15","gene_symbol":"SRRM3","gene_name":"serine/arginine repetitive matrix 3 [Source:HGNC Symbol;Acc:HGNC:26729]","synonyms":"FLJ37078","biotype":"protein_coding","ncbi_id":"222183","summary":null,"start":76201900,"end":76287288,"strand":1,"description":"serine/arginine repetitive matrix 3 [Source:HGNC Symbol;Acc:HGNC:26729]"}, {"versioned_ensembl_gene_id":"ENSG00000254477.1","gene_symbol":"AP000640.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59753015,"end":59754975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271457.1","gene_symbol":"AL590229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87143854,"end":87144748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270591.1","gene_symbol":"AL049840.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":103762803,"end":103763277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182511.11","gene_symbol":"FES","gene_name":"FES proto-oncogene, tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3657]","synonyms":"FPS","biotype":"protein_coding","ncbi_id":"2242","summary":"This gene encodes the human cellular counterpart of a feline sarcoma retrovirus protein with transforming capabilities. The gene product has tyrosine-specific protein kinase activity and that activity is required for maintenance of cellular transformation. Its chromosomal location has linked it to a specific translocation event identified in patients with acute promyelocytic leukemia but it is also involved in normal hematopoiesis as well as growth factor and cytokine receptor signaling. Alternative splicing results in multiple variants encoding different isoforms.[provided by RefSeq, Jan 2009]","start":90883695,"end":90895776,"strand":1,"description":"FES proto-oncogene, tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3657]"}, {"versioned_ensembl_gene_id":"ENSG00000084652.15","gene_symbol":"TXLNA","gene_name":"taxilin alpha [Source:HGNC Symbol;Acc:HGNC:30685]","synonyms":"DKFZp451J0118","biotype":"protein_coding","ncbi_id":"200081","summary":null,"start":32179686,"end":32198285,"strand":1,"description":"taxilin alpha [Source:HGNC Symbol;Acc:HGNC:30685]"}, {"versioned_ensembl_gene_id":"ENSG00000171723.15","gene_symbol":"GPHN","gene_name":"gephyrin [Source:HGNC Symbol;Acc:HGNC:15465]","synonyms":"KIAA1385","biotype":"protein_coding","ncbi_id":"10243","summary":"This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described; however, the full-length nature of all transcript variants is not currently known. [provided by RefSeq, Jul 2008]","start":66507407,"end":67181803,"strand":1,"description":"gephyrin [Source:HGNC Symbol;Acc:HGNC:15465]"}, {"versioned_ensembl_gene_id":"ENSG00000024422.11","gene_symbol":"EHD2","gene_name":"EH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:3243]","synonyms":"PAST2","biotype":"protein_coding","ncbi_id":"30846","summary":"This gene encodes a member of the EH domain-containing protein family. These proteins are characterized by a C-terminal EF-hand domain, a nucleotide-binding consensus site at the N terminus and a bipartite nuclear localization signal. The encoded protein interacts with the actin cytoskeleton through an N-terminal domain and also binds to an EH domain-binding protein through the C-terminal EH domain. This interaction appears to connect clathrin-dependent endocytosis to actin, suggesting that this gene product participates in the endocytic pathway. [provided by RefSeq, Jul 2008]","start":47713343,"end":47743134,"strand":1,"description":"EH domain containing 2 [Source:HGNC Symbol;Acc:HGNC:3243]"}, {"versioned_ensembl_gene_id":"ENSG00000227667.1","gene_symbol":"AL392003.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":162979551,"end":162979793,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171772.16","gene_symbol":"SYCE1","gene_name":"synaptonemal complex central element protein 1 [Source:HGNC Symbol;Acc:HGNC:28852]","synonyms":"CT76,C10orf94,bA108K14.6","biotype":"protein_coding","ncbi_id":"93426","summary":"This gene encodes a member of the synaptonemal complex, which links homologous chromosomes during prophase I of meiosis. The tripartite structure of the complex is highly conserved amongst metazoans. It consists of two lateral elements and a central region formed by transverse elements and a central element. The protein encoded by this gene localizes to the central element and is required for initiation and elongation of the synapsis. Allelic variants of this gene have been associated with premature ovarian failure and spermatogenic failure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":133553901,"end":133569835,"strand":-1,"description":"synaptonemal complex central element protein 1 [Source:HGNC Symbol;Acc:HGNC:28852]"}, {"versioned_ensembl_gene_id":"ENSG00000237798.1","gene_symbol":"AC010894.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174575227,"end":174587726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280618.2","gene_symbol":"CYFIP1","gene_name":"cytoplasmic FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13759]","synonyms":"P140SRA-1,KIAA0068,SHYC","biotype":"protein_coding","ncbi_id":"23191","summary":"This gene encodes a protein that regulates cytoskeletal dynamics and protein translation. The encoded protein is a component of the WAVE regulatory complex (WRC), which promotes actin polymerization.This protein also interacts with the Fragile X mental retardation protein (FMRP) and translation initiation factor 4E to inhibit protein translation. A large chromosomal deletion including this gene is associated with increased risk of schizophrenia and epilepsy in human patients. Reduced expression of this gene has been observed in various human cancers and the encoded protein may inhibit tumor invasion. [provided by RefSeq, May 2017]","start":22903706,"end":22981018,"strand":-1,"description":"cytoplasmic FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13759]"}, {"versioned_ensembl_gene_id":"ENSG00000151746.13","gene_symbol":"BICD1","gene_name":"BICD cargo adaptor 1 [Source:HGNC Symbol;Acc:HGNC:1049]","synonyms":null,"biotype":"protein_coding","ncbi_id":"636","summary":"This gene encodes an adaptor protein that belongs to the bicaudal D family of dynein cargo adaptors. The encoded protein acts as an intracellular cargo transport cofactor that regulates the microtubule-based loading of cargo onto the dynein motor complex. It also controls dynein motor activity and coordination. It has a domain architecture consisting of coiled-coil domains at the N- and C-termini that are highly conserved in other family members. Naturally occurring mutations in this gene are associated with short telomere length and emphysema. [provided by RefSeq, Aug 2017]","start":32106835,"end":32383633,"strand":1,"description":"BICD cargo adaptor 1 [Source:HGNC Symbol;Acc:HGNC:1049]"}, {"versioned_ensembl_gene_id":"ENSG00000162650.16","gene_symbol":"ATXN7L2","gene_name":"ataxin 7 like 2 [Source:HGNC Symbol;Acc:HGNC:28713]","synonyms":"FLJ00381,MGC46534","biotype":"protein_coding","ncbi_id":"127002","summary":null,"start":109483479,"end":109492804,"strand":1,"description":"ataxin 7 like 2 [Source:HGNC Symbol;Acc:HGNC:28713]"}, {"versioned_ensembl_gene_id":"ENSG00000276136.1","gene_symbol":"AC016957.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32000375,"end":32001222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196684.12","gene_symbol":"HSH2D","gene_name":"hematopoietic SH2 domain containing [Source:HGNC Symbol;Acc:HGNC:24920]","synonyms":"HSH2,FLJ14886,ALX","biotype":"protein_coding","ncbi_id":"84941","summary":"T-cell activation requires 2 signals: recognition of antigen by the T-cell receptor (see TCR; MIM 186880) and a costimulatory signal provided primarily by CD28 (MIM 186760) in naive T cells. HSH2 is a target of both of these signaling pathways (Greene et al., 2003 [PubMed 12960172]).[supplied by OMIM, Mar 2008]","start":16134028,"end":16158575,"strand":1,"description":"hematopoietic SH2 domain containing [Source:HGNC Symbol;Acc:HGNC:24920]"}, {"versioned_ensembl_gene_id":"ENSG00000198258.10","gene_symbol":"UBL5","gene_name":"ubiquitin like 5 [Source:HGNC Symbol;Acc:HGNC:13736]","synonyms":null,"biotype":"protein_coding","ncbi_id":"59286","summary":"This gene encodes a member of a group of proteins similar to ubiquitin. The encoded protein is not thought to degrade proteins like ubiquitin but to affect their function through being bound to target proteins by an isopeptide bond. The gene product has been studied as a link to predisposition to obesity based on its expression in Psammomys obesus, the fat sand rat, which is an animal model for obesity studies. Variation in this gene was found to be significantly associated with some metabolic traits (PMID: 15331561) but not associated with childhood obesity (PMID: 19189687). Pseudogenes of this gene are located on chromosomes 3, 5 and 17. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]","start":9827892,"end":9830115,"strand":1,"description":"ubiquitin like 5 [Source:HGNC Symbol;Acc:HGNC:13736]"}, {"versioned_ensembl_gene_id":"ENSG00000167461.11","gene_symbol":"RAB8A","gene_name":"RAB8A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:7007]","synonyms":"RAB8,MEL","biotype":"protein_coding","ncbi_id":"4218","summary":"The protein encoded by this gene is a member of the RAS superfamily which are small GTP/GDP-binding proteins with an average size of 200 amino acids. The RAS-related proteins of the RAB/YPT family may play a role in the transport of proteins from the endoplasmic reticulum to the Golgi and the plasma membrane. This protein shares 97%, 96%, and 51% similarity with the dog RAB8, mouse MEL, and mouse YPT1 proteins, respectively and contains the 4 GTP/GDP-binding sites that are present in all the RAS proteins. The putative effector-binding site of this protein is similar to that of the RAB/YPT proteins. However, this protein contains a C-terminal CAAX motif that is characteristic of many RAS superfamily members but which is not found in YPT1 and the majority of RAB proteins. Although this gene was isolated as a transforming gene from a melanoma cell line, no linkage between MEL and malignant melanoma has been demonstrable. This oncogene is located 800 kb distal to MY09B on chromosome 19p13.1. [provided by RefSeq, Jul 2008]","start":16111629,"end":16134234,"strand":1,"description":"RAB8A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:7007]"}, {"versioned_ensembl_gene_id":"ENSG00000226925.1","gene_symbol":"AC007271.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102172621,"end":102182108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167614.13","gene_symbol":"TTYH1","gene_name":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57348","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-independent, volume-sensitive large conductance chloride(-) channel. Three transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jan 2011]","start":54415219,"end":54436900,"strand":1,"description":"tweety family member 1 [Source:HGNC Symbol;Acc:HGNC:13476]"}, {"versioned_ensembl_gene_id":"ENSG00000124588.19","gene_symbol":"NQO2","gene_name":"N-ribosyldihydronicotinamide:quinone reductase 2 [Source:HGNC Symbol;Acc:HGNC:7856]","synonyms":"DIA6,DHQV,QR2,NMOR2","biotype":"protein_coding","ncbi_id":"4835","summary":"This gene encodes a member of the thioredoxin family of enzymes. It is a cytosolic and ubiquitously expressed flavoprotein that catalyzes the two-electron reduction of quinone substrates and uses dihydronicotinamide riboside as a reducing coenzyme. Mutations in this gene have been associated with neurodegenerative diseases and several cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":2987987,"end":3028869,"strand":1,"description":"N-ribosyldihydronicotinamide:quinone reductase 2 [Source:HGNC Symbol;Acc:HGNC:7856]"}, {"versioned_ensembl_gene_id":"ENSG00000182199.10","gene_symbol":"SHMT2","gene_name":"serine hydroxymethyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10852]","synonyms":"SHMT","biotype":"protein_coding","ncbi_id":"6472","summary":"This gene encodes the mitochondrial form of a pyridoxal phosphate-dependent enzyme that catalyzes the reversible reaction of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. The encoded product is primarily responsible for glycine synthesis. The activity of the encoded protein has been suggested to be the primary source of intracellular glycine. The gene which encodes the cytosolic form of this enzyme is located on chromosome 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":57229327,"end":57234935,"strand":1,"description":"serine hydroxymethyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10852]"}, {"versioned_ensembl_gene_id":"ENSG00000226649.1","gene_symbol":"AC019118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3156756,"end":3157797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112282.17","gene_symbol":"MED23","gene_name":"mediator complex subunit 23 [Source:HGNC Symbol;Acc:HGNC:2372]","synonyms":"Sur2,DRIP130,CRSP3,CRSP130","biotype":"protein_coding","ncbi_id":"9439","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein also acts as a metastasis suppressor. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2012]","start":131573966,"end":131628229,"strand":-1,"description":"mediator complex subunit 23 [Source:HGNC Symbol;Acc:HGNC:2372]"}, {"versioned_ensembl_gene_id":"ENSG00000234574.1","gene_symbol":"CR759838.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30265236,"end":30267045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227016.3","gene_symbol":"AL583808.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72765031,"end":72791282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135441.7","gene_symbol":"BLOC1S1","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:4200]","synonyms":"GCN5L1,BORCS1,BLOS1","biotype":"protein_coding","ncbi_id":"2647","summary":"BLOC1S1 is a component of the ubiquitously expressed BLOC1 multisubunit protein complex. BLOC1 is required for normal biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes and platelet dense granules (Starcevic and Dell'Angelica, 2004 [PubMed 15102850]).[supplied by OMIM, Mar 2008]","start":55716037,"end":55720087,"strand":1,"description":"biogenesis of lysosomal organelles complex 1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:4200]"}, {"versioned_ensembl_gene_id":"ENSG00000268009.5","gene_symbol":"SSX4","gene_name":"SSX family member 4 [Source:HGNC Symbol;Acc:HGNC:11338]","synonyms":"CT5.4","biotype":"protein_coding","ncbi_id":"6759","summary":"The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. Chromosome Xp11 contains a segmental duplication resulting in two identical copies of synovial sarcoma, X breakpoint 4, SSX4 and SSX4B, in tail-to-tail orientation. This gene, SSX4, represents the more telomeric copy. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":48383516,"end":48393347,"strand":1,"description":"SSX family member 4 [Source:HGNC Symbol;Acc:HGNC:11338]"}, {"versioned_ensembl_gene_id":"ENSG00000234461.1","gene_symbol":"CR753812.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31020962,"end":31025761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238212.2","gene_symbol":"LINC02096","gene_name":"long intergenic non-protein coding RNA 2096 [Source:HGNC Symbol;Acc:HGNC:52947]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984977","summary":null,"start":14834638,"end":14900554,"strand":1,"description":"long intergenic non-protein coding RNA 2096 [Source:HGNC Symbol;Acc:HGNC:52947]"}, {"versioned_ensembl_gene_id":"ENSG00000282751.1","gene_symbol":"ATP5G1P1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]","synonyms":"ATP5GP3","biotype":"processed_pseudogene","ncbi_id":"319136","summary":null,"start":105536861,"end":105537239,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19815]"}, {"versioned_ensembl_gene_id":"ENSG00000234006.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478957","summary":null,"start":31542304,"end":31543138,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000185122.10","gene_symbol":"HSF1","gene_name":"heat shock transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:5224]","synonyms":"HSTF1","biotype":"protein_coding","ncbi_id":"3297","summary":"The product of this gene is a transcription factor that is rapidly induced after temperature stress and binds heat shock promoter elements (HSE). This protein plays a role in the regulation of lifespan. Expression of this gene is repressed by phosphorylation, which promotes binding by heat shock protein 90. [provided by RefSeq, Jul 2017]","start":144291591,"end":144314722,"strand":1,"description":"heat shock transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:5224]"}, {"versioned_ensembl_gene_id":"ENSG00000135837.15","gene_symbol":"CEP350","gene_name":"centrosomal protein 350 [Source:HGNC Symbol;Acc:HGNC:24238]","synonyms":"KIAA0480,CAP350","biotype":"protein_coding","ncbi_id":"9857","summary":"The product of this gene is a large protein with a CAP-Gly domain typically found in cytoskeleton-associated proteins. The encoded protein primarily localizes to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. The encoded protein directly interacts with another large centrosomal protein and is required to anchor microtubules at the centrosome. It is also implicated in the regulation of a class of nuclear hormone receptors in the nucleus. Several alternatively spliced transcript variants have been found, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":179954738,"end":180114880,"strand":1,"description":"centrosomal protein 350 [Source:HGNC Symbol;Acc:HGNC:24238]"}, {"versioned_ensembl_gene_id":"ENSG00000260702.2","gene_symbol":"AL031713.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1103280,"end":1105461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226318.1","gene_symbol":"RPS3AP38","gene_name":"ribosomal protein S3a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36145]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271594","summary":null,"start":67960702,"end":67961464,"strand":-1,"description":"ribosomal protein S3a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36145]"}, {"versioned_ensembl_gene_id":"ENSG00000185479.5","gene_symbol":"KRT6B","gene_name":"keratin 6B [Source:HGNC Symbol;Acc:HGNC:6444]","synonyms":"KRTL1","biotype":"protein_coding","ncbi_id":"3854","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. As many as six of this type II cytokeratin (KRT6) have been identified; the multiplicity of the genes is attributed to successive gene duplication events. The genes are expressed with family members KRT16 and/or KRT17 in the filiform papillae of the tongue, the stratified epithelial lining of oral mucosa and esophagus, the outer root sheath of hair follicles, and the glandular epithelia. Mutations in these genes have been associated with pachyonychia congenita. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]","start":52446651,"end":52452126,"strand":-1,"description":"keratin 6B [Source:HGNC Symbol;Acc:HGNC:6444]"}, {"versioned_ensembl_gene_id":"ENSG00000112137.17","gene_symbol":"PHACTR1","gene_name":"phosphatase and actin regulator 1 [Source:HGNC Symbol;Acc:HGNC:20990]","synonyms":"RPEL1,KIAA1733,dJ257A7.2","biotype":"protein_coding","ncbi_id":"221692","summary":"The protein encoded by this gene is a member of the phosphatase and actin regulator family of proteins. This family member can bind actin and regulate the reorganization of the actin cytoskeleton. It plays a role in tubule formation and in endothelial cell survival. Polymorphisms in this gene are associated with susceptibility to myocardial infarction, coronary artery disease and cervical artery dissection. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":12716805,"end":13290484,"strand":1,"description":"phosphatase and actin regulator 1 [Source:HGNC Symbol;Acc:HGNC:20990]"}, {"versioned_ensembl_gene_id":"ENSG00000256851.1","gene_symbol":"AL663061.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31515979,"end":31516211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179899.8","gene_symbol":"PHC1P1","gene_name":"polyhomeotic homolog 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34502]","synonyms":"PHC1B","biotype":"processed_pseudogene","ncbi_id":"653441","summary":null,"start":55411727,"end":55414787,"strand":-1,"description":"polyhomeotic homolog 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34502]"}, {"versioned_ensembl_gene_id":"ENSG00000109466.13","gene_symbol":"KLHL2","gene_name":"kelch like family member 2 [Source:HGNC Symbol;Acc:HGNC:6353]","synonyms":"MAV","biotype":"protein_coding","ncbi_id":"11275","summary":null,"start":165207618,"end":165323156,"strand":1,"description":"kelch like family member 2 [Source:HGNC Symbol;Acc:HGNC:6353]"}, {"versioned_ensembl_gene_id":"ENSG00000144550.12","gene_symbol":"CPNE9","gene_name":"copine family member 9 [Source:HGNC Symbol;Acc:HGNC:24336]","synonyms":"KIAA4217","biotype":"protein_coding","ncbi_id":"151835","summary":null,"start":9703807,"end":9729908,"strand":1,"description":"copine family member 9 [Source:HGNC Symbol;Acc:HGNC:24336]"}, {"versioned_ensembl_gene_id":"ENSG00000101216.10","gene_symbol":"GMEB2","gene_name":"glucocorticoid modulatory element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4371]","synonyms":"P79PIF,KIAA1269,PIF79","biotype":"protein_coding","ncbi_id":"26205","summary":"This gene is a member of KDWK gene family. The product of this gene associates with GMEB1 protein, and the complex is essential for parvovirus DNA replication. Study of rat homolog implicates the role of this gene in modulation of transactivation by the glucocorticoid receptor bound to glucocorticoid response elements. This gene appears to use multiple polyadenylation sites. [provided by RefSeq, Jul 2008]","start":63587602,"end":63627041,"strand":-1,"description":"glucocorticoid modulatory element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4371]"}, {"versioned_ensembl_gene_id":"ENSG00000263761.2","gene_symbol":"GDF2","gene_name":"growth differentiation factor 2 [Source:HGNC Symbol;Acc:HGNC:4217]","synonyms":"BMP9,BMP-9","biotype":"protein_coding","ncbi_id":"2658","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates cartilage and bone development, angiogenesis and differentiation of cholinergic central nervous system neurons. Mutations in this gene are associated with hereditary hemorrhagic telangiectasia. [provided by RefSeq, Jul 2016]","start":47322490,"end":47326270,"strand":1,"description":"growth differentiation factor 2 [Source:HGNC Symbol;Acc:HGNC:4217]"}, {"versioned_ensembl_gene_id":"ENSG00000145708.10","gene_symbol":"CRHBP","gene_name":"corticotropin releasing hormone binding protein [Source:HGNC Symbol;Acc:HGNC:2356]","synonyms":"CRFBP,CRF-BP","biotype":"protein_coding","ncbi_id":"1393","summary":"Corticotropin-releasing hormone is a potent stimulator of synthesis and secretion of preopiomelanocortin-derived peptides. Although CRH concentrations in the human peripheral circulation are normally low, they increase throughout pregnancy and fall rapidly after parturition. Maternal plasma CRH probably originates from the placenta. Human plasma contains a CRH-binding protein which inactivates CRH and which may prevent inappropriate pituitary-adrenal stimulation in pregnancy. [provided by RefSeq, Jul 2008]","start":76952713,"end":76981158,"strand":1,"description":"corticotropin releasing hormone binding protein [Source:HGNC Symbol;Acc:HGNC:2356]"}, {"versioned_ensembl_gene_id":"ENSG00000267038.1","gene_symbol":"AC105094.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61681653,"end":61682695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178412.4","gene_symbol":"AC068473.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79638928,"end":79679745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177192.13","gene_symbol":"PUS1","gene_name":"pseudouridylate synthase 1 [Source:HGNC Symbol;Acc:HGNC:15508]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80324","summary":"This gene encodes a pseudouridine synthase that converts uridine to pseudouridine once it has been incorporated into an RNA molecule. The encoded enzyme may play an essential role in tRNA function and in stabilizing the secondary and tertiary structure of many RNAs. A mutation in this gene has been linked to mitochondrial myopathy and sideroblastic anemia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]","start":131929200,"end":131945896,"strand":1,"description":"pseudouridylate synthase 1 [Source:HGNC Symbol;Acc:HGNC:15508]"}, {"versioned_ensembl_gene_id":"ENSG00000215807.4","gene_symbol":"KRT18P65","gene_name":"keratin 18 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:48892]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442249","summary":null,"start":112361437,"end":112362722,"strand":-1,"description":"keratin 18 pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:48892]"}, {"versioned_ensembl_gene_id":"ENSG00000184226.14","gene_symbol":"PCDH9","gene_name":"protocadherin 9 [Source:HGNC Symbol;Acc:HGNC:8661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5101","summary":"This gene encodes a member of the protocadherin family, and cadherin superfamily, of transmembrane proteins containing cadherin domains. These proteins mediate cell adhesion in neural tissues in the presence of calcium. The encoded protein may be involved in signaling at neuronal synaptic junctions. Sharing a characteristic with other protocadherin genes, this gene has a notably large exon that encodes multiple cadherin domains and a transmembrane region. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Nov 2012]","start":66302834,"end":67230445,"strand":-1,"description":"protocadherin 9 [Source:HGNC Symbol;Acc:HGNC:8661]"}, {"versioned_ensembl_gene_id":"ENSG00000180673.9","gene_symbol":"EXOC5P1","gene_name":"exocyst complex component 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43870]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644548","summary":null,"start":62816826,"end":62818794,"strand":1,"description":"exocyst complex component 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43870]"}, {"versioned_ensembl_gene_id":"ENSG00000265451.1","gene_symbol":"AC012447.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121530422,"end":121532705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090013.9","gene_symbol":"BLVRB","gene_name":"biliverdin reductase B [Source:HGNC Symbol;Acc:HGNC:1063]","synonyms":"SDR43U1,FLR","biotype":"protein_coding","ncbi_id":"645","summary":"The final step in heme metabolism in mammals is catalyzed by the cytosolic biliverdin reductase enzymes A and B (EC 1.3.1.24).[supplied by OMIM, Jul 2009]","start":40447789,"end":40465840,"strand":-1,"description":"biliverdin reductase B [Source:HGNC Symbol;Acc:HGNC:1063]"}, {"versioned_ensembl_gene_id":"ENSG00000272141.1","gene_symbol":"AL390719.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1169357,"end":1170343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214891.9","gene_symbol":"TRIM64C","gene_name":"tripartite motif containing 64C [Source:HGNC Symbol;Acc:HGNC:37148]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646754","summary":null,"start":49053714,"end":49059112,"strand":-1,"description":"tripartite motif containing 64C [Source:HGNC Symbol;Acc:HGNC:37148]"}, {"versioned_ensembl_gene_id":"ENSG00000223625.1","gene_symbol":"CYCSP32","gene_name":"cytochrome c, somatic pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:24406]","synonyms":"HCP32","biotype":"processed_pseudogene","ncbi_id":"360181","summary":null,"start":19458398,"end":19458718,"strand":-1,"description":"cytochrome c, somatic pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:24406]"}, {"versioned_ensembl_gene_id":"ENSG00000115263.14","gene_symbol":"GCG","gene_name":"glucagon [Source:HGNC Symbol;Acc:HGNC:4191]","synonyms":"GRPP,GLP2,GLP1,GLP-1","biotype":"protein_coding","ncbi_id":"2641","summary":"The protein encoded by this gene is actually a preproprotein that is cleaved into four distinct mature peptides. One of these, glucagon, is a pancreatic hormone that counteracts the glucose-lowering action of insulin by stimulating glycogenolysis and gluconeogenesis. Glucagon is a ligand for a specific G-protein linked receptor whose signalling pathway controls cell proliferation. Two of the other peptides are secreted from gut endocrine cells and promote nutrient absorption through distinct mechanisms. Finally, the fourth peptide is similar to glicentin, an active enteroglucagon. [provided by RefSeq, Jul 2008]","start":162142873,"end":162152404,"strand":-1,"description":"glucagon [Source:HGNC Symbol;Acc:HGNC:4191]"}, {"versioned_ensembl_gene_id":"ENSG00000274685.1","gene_symbol":"AL360181.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":133374736,"end":133374869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132773.11","gene_symbol":"TOE1","gene_name":"target of EGR1, member 1 (nuclear) [Source:HGNC Symbol;Acc:HGNC:15954]","synonyms":"hCaf1z","biotype":"protein_coding","ncbi_id":"114034","summary":null,"start":45339670,"end":45343975,"strand":1,"description":"target of EGR1, member 1 (nuclear) [Source:HGNC Symbol;Acc:HGNC:15954]"}, {"versioned_ensembl_gene_id":"ENSG00000247775.2","gene_symbol":"SNCA-AS1","gene_name":"SNCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50600]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644248","summary":null,"start":89836408,"end":89841978,"strand":1,"description":"SNCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50600]"}, {"versioned_ensembl_gene_id":"ENSG00000236014.10","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"SACM2L,ARE1","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33390441,"end":33412193,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000284711.1","gene_symbol":"AC010325.3","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":50808145,"end":50812707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233197.1","gene_symbol":"TMEM256P1","gene_name":"transmembrane protein 256 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45087]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645269","summary":null,"start":69523311,"end":69523650,"strand":-1,"description":"transmembrane protein 256 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45087]"}, {"versioned_ensembl_gene_id":"ENSG00000234251.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"HTATSF1P,dJ1033B10.6,TAT-SF1-L","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33377903,"end":33379802,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000225696.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33355816,"end":33356439,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000258964.1","gene_symbol":"AL137129.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61734138,"end":61776260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129219.13","gene_symbol":"PLD2","gene_name":"phospholipase D2 [Source:HGNC Symbol;Acc:HGNC:9068]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5338","summary":"The protein encoded by this gene catalyzes the hydrolysis of phosphatidylcholine to phosphatidic acid and choline. The activity of the encoded enzyme is enhanced by phosphatidylinositol 4,5-bisphosphate and ADP-ribosylation factor-1. This protein localizes to the peripheral membrane and may be involved in cytoskeletal organization, cell cycle control, transcriptional regulation, and/or regulated secretion. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]","start":4807096,"end":4823434,"strand":1,"description":"phospholipase D2 [Source:HGNC Symbol;Acc:HGNC:9068]"}, {"versioned_ensembl_gene_id":"ENSG00000217707.2","gene_symbol":"SERPINB8P1","gene_name":"serpin family B member 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8953]","synonyms":"SERPINBP1,SERPINB11,PI8L1","biotype":"unprocessed_pseudogene","ncbi_id":"11029","summary":null,"start":3048835,"end":3049211,"strand":1,"description":"serpin family B member 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8953]"}, {"versioned_ensembl_gene_id":"ENSG00000166592.11","gene_symbol":"RRAD","gene_name":"RRAD, Ras related glycolysis inhibitor and calcium channel regulator [Source:HGNC Symbol;Acc:HGNC:10446]","synonyms":"REM3,RAD","biotype":"protein_coding","ncbi_id":"6236","summary":null,"start":66921679,"end":66925644,"strand":-1,"description":"RRAD, Ras related glycolysis inhibitor and calcium channel regulator [Source:HGNC Symbol;Acc:HGNC:10446]"}, {"versioned_ensembl_gene_id":"ENSG00000127952.16","gene_symbol":"STYXL1","gene_name":"serine/threonine/tyrosine interacting like 1 [Source:HGNC Symbol;Acc:HGNC:18165]","synonyms":"MK-STYX,DUSP24","biotype":"protein_coding","ncbi_id":"51657","summary":null,"start":75996338,"end":76048004,"strand":-1,"description":"serine/threonine/tyrosine interacting like 1 [Source:HGNC Symbol;Acc:HGNC:18165]"}, {"versioned_ensembl_gene_id":"ENSG00000254764.1","gene_symbol":"TRIM53CP","gene_name":"tripartite motif containing 53C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43979]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"340970","summary":null,"start":48985871,"end":48991881,"strand":-1,"description":"tripartite motif containing 53C, pseudogene [Source:HGNC Symbol;Acc:HGNC:43979]"}, {"versioned_ensembl_gene_id":"ENSG00000278145.2","gene_symbol":"C17orf78","gene_name":"chromosome 17 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:26831]","synonyms":"FLJ39647","biotype":"protein_coding","ncbi_id":"284099","summary":null,"start":37377461,"end":37394195,"strand":1,"description":"chromosome 17 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:26831]"}, {"versioned_ensembl_gene_id":"ENSG00000112357.12","gene_symbol":"PEX7","gene_name":"peroxisomal biogenesis factor 7 [Source:HGNC Symbol;Acc:HGNC:8860]","synonyms":"RD,PTS2R","biotype":"protein_coding","ncbi_id":"5191","summary":"This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008]","start":136822564,"end":136913937,"strand":1,"description":"peroxisomal biogenesis factor 7 [Source:HGNC Symbol;Acc:HGNC:8860]"}, {"versioned_ensembl_gene_id":"ENSG00000228432.1","gene_symbol":"DHFRP2","gene_name":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729816","summary":null,"start":31366352,"end":31366898,"strand":-1,"description":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]"}, {"versioned_ensembl_gene_id":"ENSG00000233009.1","gene_symbol":"NALCN-AS1","gene_name":"NALCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42743]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885778","summary":null,"start":100708325,"end":101059286,"strand":1,"description":"NALCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42743]"}, {"versioned_ensembl_gene_id":"ENSG00000276744.1","gene_symbol":"AC105137.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75452964,"end":75453947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219149.4","gene_symbol":"AL161626.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76549282,"end":76549771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132329.10","gene_symbol":"RAMP1","gene_name":"receptor activity modifying protein 1 [Source:HGNC Symbol;Acc:HGNC:9843]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10267","summary":"The protein encoded by this gene is a member of the RAMP family of single-transmembrane-domain proteins, called receptor (calcitonin) activity modifying proteins (RAMPs). RAMPs are type I transmembrane proteins with an extracellular N terminus and a cytoplasmic C terminus. RAMPs are required to transport calcitonin-receptor-like receptor (CRLR) to the plasma membrane. CRLR, a receptor with seven transmembrane domains, can function as either a calcitonin-gene-related peptide (CGRP) receptor or an adrenomedullin receptor, depending on which members of the RAMP family are expressed. In the presence of this (RAMP1) protein, CRLR functions as a CGRP receptor. The RAMP1 protein is involved in the terminal glycosylation, maturation, and presentation of the CGRP receptor to the cell surface. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":237858893,"end":237912114,"strand":1,"description":"receptor activity modifying protein 1 [Source:HGNC Symbol;Acc:HGNC:9843]"}, {"versioned_ensembl_gene_id":"ENSG00000236941.6","gene_symbol":"AC106872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164948079,"end":164949438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229453.2","gene_symbol":"SPINK8","gene_name":"serine peptidase inhibitor, Kazal type 8 (putative) [Source:HGNC Symbol;Acc:HGNC:33160]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646424","summary":null,"start":48306842,"end":48328341,"strand":-1,"description":"serine peptidase inhibitor, Kazal type 8 (putative) [Source:HGNC Symbol;Acc:HGNC:33160]"}, {"versioned_ensembl_gene_id":"ENSG00000279962.1","gene_symbol":"AP001525.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":13710249,"end":13710484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229075.1","gene_symbol":"BX088580.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31195054,"end":31196805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226271.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29111918,"end":29112853,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000232789.1","gene_symbol":"AC053503.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":219358870,"end":219358983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116668.12","gene_symbol":"SWT1","gene_name":"SWT1, RNA endoribonuclease homolog [Source:HGNC Symbol;Acc:HGNC:16785]","synonyms":"HsSwt1,FLJ20121,C1orf26","biotype":"protein_coding","ncbi_id":"54823","summary":null,"start":185157080,"end":185291765,"strand":1,"description":"SWT1, RNA endoribonuclease homolog [Source:HGNC Symbol;Acc:HGNC:16785]"}, {"versioned_ensembl_gene_id":"ENSG00000243649.8","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31945650,"end":31952084,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000271143.1","gene_symbol":"AL357137.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115916497,"end":115916699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250416.2","gene_symbol":"SEC63P2","gene_name":"SEC63 homolog, protein translocation regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41954]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420287","summary":null,"start":35487812,"end":35489750,"strand":1,"description":"SEC63 homolog, protein translocation regulator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41954]"}, {"versioned_ensembl_gene_id":"ENSG00000151743.10","gene_symbol":"AMN1","gene_name":"antagonist of mitotic exit network 1 homolog [Source:HGNC Symbol;Acc:HGNC:27281]","synonyms":null,"biotype":"protein_coding","ncbi_id":"196394","summary":null,"start":31671137,"end":31729174,"strand":-1,"description":"antagonist of mitotic exit network 1 homolog [Source:HGNC Symbol;Acc:HGNC:27281]"}, {"versioned_ensembl_gene_id":"ENSG00000109929.9","gene_symbol":"SC5D","gene_name":"sterol-C5-desaturase [Source:HGNC Symbol;Acc:HGNC:10547]","synonyms":"SC5DL","biotype":"protein_coding","ncbi_id":"6309","summary":"This gene encodes an enzyme of cholesterol biosynthesis. The encoded protein catalyzes the conversion of lathosterol into 7-dehydrocholesterol. Mutations in this gene have been associated with lathosterolosis. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":121292453,"end":121308694,"strand":1,"description":"sterol-C5-desaturase [Source:HGNC Symbol;Acc:HGNC:10547]"}, {"versioned_ensembl_gene_id":"ENSG00000279080.1","gene_symbol":"AL022322.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38130216,"end":38150612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160219.11","gene_symbol":"GAB3","gene_name":"GRB2 associated binding protein 3 [Source:HGNC Symbol;Acc:HGNC:17515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"139716","summary":"This gene is a member of the GRB2-associated binding protein gene family. These proteins are scaffolding/docking proteins that are involved in several growth factor and cytokine signaling pathways, and they contain a pleckstrin homology domain, and bind SHP2 tyrosine phosphatase and GRB2 adapter protein. The protein encoded by this gene facilitates macrophage differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":154675249,"end":154751583,"strand":-1,"description":"GRB2 associated binding protein 3 [Source:HGNC Symbol;Acc:HGNC:17515]"}, {"versioned_ensembl_gene_id":"ENSG00000125170.10","gene_symbol":"DOK4","gene_name":"docking protein 4 [Source:HGNC Symbol;Acc:HGNC:19868]","synonyms":"FLJ10488","biotype":"protein_coding","ncbi_id":"55715","summary":null,"start":57471922,"end":57487327,"strand":-1,"description":"docking protein 4 [Source:HGNC Symbol;Acc:HGNC:19868]"}, {"versioned_ensembl_gene_id":"ENSG00000278337.1","gene_symbol":"AL139327.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19172773,"end":19172925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072110.13","gene_symbol":"ACTN1","gene_name":"actinin alpha 1 [Source:HGNC Symbol;Acc:HGNC:163]","synonyms":null,"biotype":"protein_coding","ncbi_id":"87","summary":"Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a nonmuscle, cytoskeletal, alpha actinin isoform and maps to the same site as the structurally similar erythroid beta spectrin gene. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":68874143,"end":68979440,"strand":-1,"description":"actinin alpha 1 [Source:HGNC Symbol;Acc:HGNC:163]"}, {"versioned_ensembl_gene_id":"ENSG00000224622.1","gene_symbol":"OR9R1P","gene_name":"olfactory receptor family 9 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15340]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81140","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55158847,"end":55159723,"strand":1,"description":"olfactory receptor family 9 subfamily R member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15340]"}, {"versioned_ensembl_gene_id":"ENSG00000244400.2","gene_symbol":"RPS4XP12","gene_name":"ribosomal protein S4X pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35951]","synonyms":"RPS4P12","biotype":"processed_pseudogene","ncbi_id":"100271385","summary":null,"start":121250270,"end":121250978,"strand":-1,"description":"ribosomal protein S4X pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35951]"}, {"versioned_ensembl_gene_id":"ENSG00000249249.1","gene_symbol":"AC010226.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115602057,"end":115620659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109101.7","gene_symbol":"FOXN1","gene_name":"forkhead box N1 [Source:HGNC Symbol;Acc:HGNC:12765]","synonyms":"FKHL20,WHN,RONU","biotype":"protein_coding","ncbi_id":"8456","summary":"Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008]","start":28506243,"end":28538896,"strand":1,"description":"forkhead box N1 [Source:HGNC Symbol;Acc:HGNC:12765]"}, {"versioned_ensembl_gene_id":"ENSG00000127540.11","gene_symbol":"UQCR11","gene_name":"ubiquinol-cytochrome c reductase, complex III subunit XI [Source:HGNC Symbol;Acc:HGNC:30862]","synonyms":"UQCR,QCR10","biotype":"protein_coding","ncbi_id":"10975","summary":"This gene encodes the smallest known component of the ubiquinol-cytochrome c reductase complex, which forms part of the mitochondrial respiratory chain. The encoded protein may function as a binding factor for the iron-sulfur protein in this complex. [provided by RefSeq, Oct 2009]","start":1597172,"end":1605490,"strand":-1,"description":"ubiquinol-cytochrome c reductase, complex III subunit XI [Source:HGNC Symbol;Acc:HGNC:30862]"}, {"versioned_ensembl_gene_id":"ENSG00000104047.14","gene_symbol":"DTWD1","gene_name":"DTW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30926]","synonyms":"MGC111207,MDS009","biotype":"protein_coding","ncbi_id":"56986","summary":null,"start":49620980,"end":49656232,"strand":1,"description":"DTW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30926]"}, {"versioned_ensembl_gene_id":"ENSG00000109927.9","gene_symbol":"TECTA","gene_name":"tectorin alpha [Source:HGNC Symbol;Acc:HGNC:11720]","synonyms":"DFNB21,DFNA8,DFNA12","biotype":"protein_coding","ncbi_id":"7007","summary":"The tectorial membrane is an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells. Sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair-cell membrane potential, transducing sound into electrical signals. Alpha-tectorin is one of the major noncollagenous components of the tectorial membrane. Mutations in the TECTA gene have been shown to be responsible for autosomal dominant nonsyndromic hearing impairment and a recessive form of sensorineural pre-lingual non-syndromic deafness. [provided by RefSeq, Jul 2008]","start":121101173,"end":121191493,"strand":1,"description":"tectorin alpha [Source:HGNC Symbol;Acc:HGNC:11720]"}, {"versioned_ensembl_gene_id":"ENSG00000130640.13","gene_symbol":"TUBGCP2","gene_name":"tubulin gamma complex associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18599]","synonyms":"Spc97p,SPBC97,GCP2","biotype":"protein_coding","ncbi_id":"10844","summary":null,"start":133278630,"end":133312337,"strand":-1,"description":"tubulin gamma complex associated protein 2 [Source:HGNC Symbol;Acc:HGNC:18599]"}, {"versioned_ensembl_gene_id":"ENSG00000204653.9","gene_symbol":"ASPDH","gene_name":"aspartate dehydrogenase domain containing [Source:HGNC Symbol;Acc:HGNC:33856]","synonyms":null,"biotype":"protein_coding","ncbi_id":"554235","summary":null,"start":50511600,"end":50514690,"strand":-1,"description":"aspartate dehydrogenase domain containing [Source:HGNC Symbol;Acc:HGNC:33856]"}, {"versioned_ensembl_gene_id":"ENSG00000259086.3","gene_symbol":"AL136298.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32271857,"end":32272301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254877.1","gene_symbol":"AP001636.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58967596,"end":58968291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248722.1","gene_symbol":"AK3P4","gene_name":"adenylate kinase 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39063]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129959","summary":null,"start":115402380,"end":115402962,"strand":1,"description":"adenylate kinase 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39063]"}, {"versioned_ensembl_gene_id":"ENSG00000250723.5","gene_symbol":"AC016687.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33850591,"end":33979936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238105.7","gene_symbol":"GOLGA2P5","gene_name":"golgin A2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:25315]","synonyms":"GOLGA2L1,GOLGA2B,DKFZp434M0331","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"55592","summary":null,"start":100156357,"end":100173659,"strand":-1,"description":"golgin A2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:25315]"}, {"versioned_ensembl_gene_id":"ENSG00000169856.8","gene_symbol":"ONECUT1","gene_name":"one cut homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8138]","synonyms":"HNF6A,HNF6,HNF-6","biotype":"protein_coding","ncbi_id":"3175","summary":"This gene encodes a member of the Cut homeobox family of transcription factors. Expression of the encoded protein is enriched in the liver, where it stimulates transcription of liver-expressed genes, and antagonizes glucocorticoid-stimulated gene transcription. This gene may influence a variety of cellular processes including glucose metabolism, cell cycle regulation, and it may also be associated with cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":52756989,"end":52791078,"strand":-1,"description":"one cut homeobox 1 [Source:HGNC Symbol;Acc:HGNC:8138]"}, {"versioned_ensembl_gene_id":"ENSG00000184012.11","gene_symbol":"TMPRSS2","gene_name":"transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:11876]","synonyms":"PRSS10","biotype":"protein_coding","ncbi_id":"7113","summary":"This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a type II transmembrane domain, a receptor class A domain, a scavenger receptor cysteine-rich domain and a protease domain. Serine proteases are known to be involved in many physiological and pathological processes. This gene was demonstrated to be up-regulated by androgenic hormones in prostate cancer cells and down-regulated in androgen-independent prostate cancer tissue. The protease domain of this protein is thought to be cleaved and secreted into cell media after autocleavage. This protein also facilitates entry of viruses into host cells by proteolytically cleaving and activating viral envelope glycoproteins. Viruses found to use this protein for cell entry include Influenza virus and the human coronaviruses HCoV-229E, MERS-CoV, SARS-CoV and SARS-CoV-2 (COVID-19 virus). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2020]","start":41464551,"end":41531116,"strand":-1,"description":"transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:11876]"}, {"versioned_ensembl_gene_id":"ENSG00000219926.11","gene_symbol":"AL445238.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63828840,"end":63844125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154548.8","gene_symbol":"SRSF12","gene_name":"serine and arginine rich splicing factor 12 [Source:HGNC Symbol;Acc:HGNC:21220]","synonyms":"SRrp35,SFRS19,SFRS13B","biotype":"protein_coding","ncbi_id":"135295","summary":null,"start":89095959,"end":89118081,"strand":-1,"description":"serine and arginine rich splicing factor 12 [Source:HGNC Symbol;Acc:HGNC:21220]"}, {"versioned_ensembl_gene_id":"ENSG00000279539.1","gene_symbol":"AC006486.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":42242775,"end":42244973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006459.10","gene_symbol":"KDM7A","gene_name":"lysine demethylase 7A [Source:HGNC Symbol;Acc:HGNC:22224]","synonyms":"KIAA1718,JHDM1D","biotype":"protein_coding","ncbi_id":"80853","summary":null,"start":140084746,"end":140177035,"strand":-1,"description":"lysine demethylase 7A [Source:HGNC Symbol;Acc:HGNC:22224]"}, {"versioned_ensembl_gene_id":"ENSG00000234124.6","gene_symbol":"CSN1S2AP","gene_name":"casein alpha s2-like A, pseudogene [Source:HGNC Symbol;Acc:HGNC:20230]","synonyms":"CSN1S2A","biotype":"transcribed_unitary_pseudogene","ncbi_id":"286828","summary":"This locus is the equivalent of casein gamma in mouse (GeneID 12993) and is found in a cluster of casein genes, similar to other mammals. In human, the potential open reading frame that matches the homologous protein from other species is prematurely truncated shortly after the signal peptide. Therefore, this locus appears to be a pseudogene. [provided by RefSeq, Jul 2008]","start":70067386,"end":70085290,"strand":1,"description":"casein alpha s2-like A, pseudogene [Source:HGNC Symbol;Acc:HGNC:20230]"}, {"versioned_ensembl_gene_id":"ENSG00000272182.1","gene_symbol":"AC135507.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58428255,"end":58428815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227818.1","gene_symbol":"AL590408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162039016,"end":162039567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277519.1","gene_symbol":"AC078938.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21817579,"end":21818218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152454.3","gene_symbol":"ZNF256","gene_name":"zinc finger protein 256 [Source:HGNC Symbol;Acc:HGNC:13049]","synonyms":"BMZF-3","biotype":"protein_coding","ncbi_id":"10172","summary":null,"start":57940833,"end":57947675,"strand":-1,"description":"zinc finger protein 256 [Source:HGNC Symbol;Acc:HGNC:13049]"}, {"versioned_ensembl_gene_id":"ENSG00000257489.6","gene_symbol":"AC010203.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":100173196,"end":100199783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270763.1","gene_symbol":"DDX43P2","gene_name":"DEAD-box helicase 43 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533714","summary":null,"start":49258493,"end":49259846,"strand":-1,"description":"DEAD-box helicase 43 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50781]"}, {"versioned_ensembl_gene_id":"ENSG00000268643.1","gene_symbol":"AC006486.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42234583,"end":42255132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263870.1","gene_symbol":"AC015917.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28444063,"end":28445563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100321.14","gene_symbol":"SYNGR1","gene_name":"synaptogyrin 1 [Source:HGNC Symbol;Acc:HGNC:11498]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9145","summary":"This gene encodes an integral membrane protein associated with presynaptic vesicles in neuronal cells. The exact function of this protein is unclear, but studies of a similar murine protein suggest that it functions in synaptic plasticity without being required for synaptic transmission. The gene product belongs to the synaptogyrin gene family. Three alternatively spliced variants encoding three different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":39349925,"end":39385588,"strand":1,"description":"synaptogyrin 1 [Source:HGNC Symbol;Acc:HGNC:11498]"}, {"versioned_ensembl_gene_id":"ENSG00000233651.2","gene_symbol":"AL590399.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62387171,"end":62394004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196433.12","gene_symbol":"ASMT","gene_name":"acetylserotonin O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:750]","synonyms":"HIOMTY,HIOMT,ASMTY","biotype":"protein_coding","ncbi_id":"438","summary":"This gene belongs to the methyltransferase superfamily, and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. The encoded enzyme catalyzes the final reaction in the synthesis of melatonin, and is abundant in the pineal gland. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2010]","start":1615001,"end":1643081,"strand":1,"description":"acetylserotonin O-methyltransferase [Source:HGNC Symbol;Acc:HGNC:750]"}, {"versioned_ensembl_gene_id":"ENSG00000237582.10","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"Oct4,OCT3,OTF3,MGC22487","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31159218,"end":31165590,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000281348.1","gene_symbol":"AC120114.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29817239,"end":29830627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254735.1","gene_symbol":"HMGB1P42","gene_name":"high mobility group box 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:39189]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873906","summary":null,"start":120936102,"end":120936654,"strand":-1,"description":"high mobility group box 1 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:39189]"}, {"versioned_ensembl_gene_id":"ENSG00000237121.1","gene_symbol":"PIEZO1P2","gene_name":"piezo type mechanosensitive ion channel component 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42861]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874493","summary":null,"start":58740532,"end":58783821,"strand":-1,"description":"piezo type mechanosensitive ion channel component 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42861]"}, {"versioned_ensembl_gene_id":"ENSG00000249943.1","gene_symbol":"AC097486.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170814339,"end":170814548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103549.21","gene_symbol":"RNF40","gene_name":"ring finger protein 40 [Source:HGNC Symbol;Acc:HGNC:16867]","synonyms":"STARING,RBP95,KIAA0661,BRE1B","biotype":"protein_coding","ncbi_id":"9810","summary":"The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein was reported to interact with the tumor suppressor protein RB1. Studies of the rat counterpart suggested that this protein may function as an E3 ubiquitin-protein ligase, and facilitate the ubiquitination and degradation of syntaxin 1, which is an essential component of the neurotransmitter release machinery. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":30761745,"end":30776307,"strand":1,"description":"ring finger protein 40 [Source:HGNC Symbol;Acc:HGNC:16867]"}, {"versioned_ensembl_gene_id":"ENSG00000250082.1","gene_symbol":"AC074255.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":170481695,"end":170482195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251061.2","gene_symbol":"LINC02512","gene_name":"long intergenic non-protein coding RNA 2512 [Source:HGNC Symbol;Acc:HGNC:53501]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986241","summary":null,"start":170343089,"end":170372311,"strand":1,"description":"long intergenic non-protein coding RNA 2512 [Source:HGNC Symbol;Acc:HGNC:53501]"}, {"versioned_ensembl_gene_id":"ENSG00000091879.13","gene_symbol":"ANGPT2","gene_name":"angiopoietin 2 [Source:HGNC Symbol;Acc:HGNC:485]","synonyms":"Ang2","biotype":"protein_coding","ncbi_id":"285","summary":"This gene belongs to the angiopoietin family of growth factors. The protein encoded by this gene is an antagonist of angiopoietin 1, and both angiopoietin 1 and angiopoietin 2 are ligands for the endothelial TEK receptor tyrosine kinase. Angiopoietin 2 is upregulated in multiple inflammatory diseases and is implicated in the direct control of inflammation-related signaling pathways. The encoded protein affects angiogenesis during embryogenesis and tumorigenesis, disrupts the vascular remodeling ability of angiopoietin 1, and may induce endothelial cell apoptosis. This gene serves a prognostic biomarker for acute respiratory distress syndrome. [provided by RefSeq, Aug 2020]","start":6499651,"end":6563409,"strand":-1,"description":"angiopoietin 2 [Source:HGNC Symbol;Acc:HGNC:485]"}, {"versioned_ensembl_gene_id":"ENSG00000232999.1","gene_symbol":"AL133351.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":2910613,"end":2912113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184860.9","gene_symbol":"SDR42E1","gene_name":"short chain dehydrogenase/reductase family 42E, member 1 [Source:HGNC Symbol;Acc:HGNC:29834]","synonyms":"HSPC105","biotype":"protein_coding","ncbi_id":"93517","summary":null,"start":81988855,"end":82011488,"strand":-1,"description":"short chain dehydrogenase/reductase family 42E, member 1 [Source:HGNC Symbol;Acc:HGNC:29834]"}, {"versioned_ensembl_gene_id":"ENSG00000179031.8","gene_symbol":"Z73417.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100910712,"end":100911489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236324.1","gene_symbol":"AL035634.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157885114,"end":157892786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141401.11","gene_symbol":"IMPA2","gene_name":"inositol monophosphatase 2 [Source:HGNC Symbol;Acc:HGNC:6051]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3613","summary":"This locus encodes an inositol monophosphatase. The encoded protein catalyzes the dephosphoylration of inositol monophosphate and plays an important role in phosphatidylinositol signaling. This locus may be associated with susceptibility to bipolar disorder. [provided by RefSeq, Jan 2011]","start":11981025,"end":12030883,"strand":1,"description":"inositol monophosphatase 2 [Source:HGNC Symbol;Acc:HGNC:6051]"}, {"versioned_ensembl_gene_id":"ENSG00000197568.13","gene_symbol":"HHLA3","gene_name":"HERV-H LTR-associating 3 [Source:HGNC Symbol;Acc:HGNC:4906]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11147","summary":null,"start":70354805,"end":70385339,"strand":1,"description":"HERV-H LTR-associating 3 [Source:HGNC Symbol;Acc:HGNC:4906]"}, {"versioned_ensembl_gene_id":"ENSG00000171478.7","gene_symbol":"SPACA5B","gene_name":"sperm acrosome associated 5B [Source:HGNC Symbol;Acc:HGNC:19142]","synonyms":"LYZL5B","biotype":"protein_coding","ncbi_id":"729201","summary":null,"start":48130657,"end":48132613,"strand":1,"description":"sperm acrosome associated 5B [Source:HGNC Symbol;Acc:HGNC:19142]"}, {"versioned_ensembl_gene_id":"ENSG00000237576.1","gene_symbol":"LINC01888","gene_name":"long intergenic non-protein coding RNA 1888 [Source:HGNC Symbol;Acc:HGNC:52707]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107985893","summary":null,"start":68832044,"end":68837724,"strand":1,"description":"long intergenic non-protein coding RNA 1888 [Source:HGNC Symbol;Acc:HGNC:52707]"}, {"versioned_ensembl_gene_id":"ENSG00000232596.2","gene_symbol":"LINC01646","gene_name":"long intergenic non-protein coding RNA 1646 [Source:HGNC Symbol;Acc:HGNC:52433]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376679","summary":null,"start":4571481,"end":4594009,"strand":1,"description":"long intergenic non-protein coding RNA 1646 [Source:HGNC Symbol;Acc:HGNC:52433]"}, {"versioned_ensembl_gene_id":"ENSG00000273687.1","gene_symbol":"AC004223.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35018660,"end":35018991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275142.1","gene_symbol":"AL132821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19871891,"end":19872284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228650.2","gene_symbol":"AC008940.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56770799,"end":56772303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253571.1","gene_symbol":"AC087369.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5848697,"end":5849692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107679.14","gene_symbol":"PLEKHA1","gene_name":"pleckstrin homology domain containing A1 [Source:HGNC Symbol;Acc:HGNC:14335]","synonyms":"TAPP1","biotype":"protein_coding","ncbi_id":"59338","summary":"This gene encodes a pleckstrin homology domain-containing adapter protein. The encoded protein is localized to the plasma membrane where it specifically binds phosphatidylinositol 3,4-bisphosphate. This protein may be involved in the formation of signaling complexes in the plasma membrane. Polymorphisms in this gene are associated with age-related macular degeneration. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 5.[provided by RefSeq, Sep 2010]","start":122374696,"end":122442602,"strand":1,"description":"pleckstrin homology domain containing A1 [Source:HGNC Symbol;Acc:HGNC:14335]"}, {"versioned_ensembl_gene_id":"ENSG00000231120.3","gene_symbol":"BTF3P10","gene_name":"basic transcription factor 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38570]","synonyms":"RAET1J","biotype":"processed_pseudogene","ncbi_id":"345829","summary":null,"start":149977922,"end":149978416,"strand":1,"description":"basic transcription factor 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38570]"}, {"versioned_ensembl_gene_id":"ENSG00000234553.1","gene_symbol":"AC022431.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56536583,"end":56537826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134200.3","gene_symbol":"TSHB","gene_name":"thyroid stimulating hormone beta [Source:HGNC Symbol;Acc:HGNC:12372]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7252","summary":"The four human glycoprotein hormones chorionic gonadotropin (CG), luteinizing hormone (LH), follicle stimulating hormone (FSH), and thyroid stimulating hormone (TSH) are dimers consisting of alpha and beta subunits that are associated noncovalently. The alpha subunits of these hormones are identical, however, their beta chains are unique and confer biological specificity. Thyroid stimulating hormone functions in the control of thyroid structure and metabolism. The protein encoded by this gene is the beta subunit of thyroid stimulating hormone. Mutations in this gene are associated with congenital central and secondary hypothyroidism and Hashimoto's thyroiditis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":115029824,"end":115034309,"strand":1,"description":"thyroid stimulating hormone beta [Source:HGNC Symbol;Acc:HGNC:12372]"}, {"versioned_ensembl_gene_id":"ENSG00000279147.1","gene_symbol":"AC112504.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":141936707,"end":141938547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170633.16","gene_symbol":"RNF34","gene_name":"ring finger protein 34 [Source:HGNC Symbol;Acc:HGNC:17297]","synonyms":"RIF,FLJ21786,RIFF","biotype":"protein_coding","ncbi_id":"80196","summary":"The protein encoded by this gene contains a RINF finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein interacts with DNAJA3/hTid-1, which is a DnaJ protein reported to function as a modulator of apoptosis. Overexpression of this gene in Hela cells was shown to confer the resistance to TNF-alpha induced apoptosis, suggesting an anti-apoptotic function of this protein. This protein can be cleaved by caspase-3 during the induction of apoptosis. This protein also targets p53 and phospho-p53 for degradation. Alternatively splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2012]","start":121400041,"end":121430623,"strand":1,"description":"ring finger protein 34 [Source:HGNC Symbol;Acc:HGNC:17297]"}, {"versioned_ensembl_gene_id":"ENSG00000205108.5","gene_symbol":"FAM205A","gene_name":"family with sequence similarity 205 member A [Source:HGNC Symbol;Acc:HGNC:41911]","synonyms":"C9orf144B","biotype":"protein_coding","ncbi_id":"259308","summary":null,"start":34723055,"end":34729467,"strand":-1,"description":"family with sequence similarity 205 member A [Source:HGNC Symbol;Acc:HGNC:41911]"}, {"versioned_ensembl_gene_id":"ENSG00000239893.1","gene_symbol":"ZNF736P9Y","gene_name":"zinc finger protein 736 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:38408]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419726","summary":null,"start":8068896,"end":8070723,"strand":-1,"description":"zinc finger protein 736 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:38408]"}, {"versioned_ensembl_gene_id":"ENSG00000226221.1","gene_symbol":"AC022431.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56504635,"end":56505072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239793.1","gene_symbol":"AC098818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78768499,"end":78768750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141096.4","gene_symbol":"DPEP3","gene_name":"dipeptidase 3 [Source:HGNC Symbol;Acc:HGNC:23029]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64180","summary":"This gene encodes a membrane-bound glycoprotein from the family of dipeptidases involved in hydrolytic metabolism of various dipeptides, including penem and carbapenem beta-lactam antibiotics. This gene is located on chromosome 16 in a cluster with another member of this family. Alternatively spliced transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":67975663,"end":67980829,"strand":-1,"description":"dipeptidase 3 [Source:HGNC Symbol;Acc:HGNC:23029]"}, {"versioned_ensembl_gene_id":"ENSG00000277114.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138182,"end":54156190,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000126746.17","gene_symbol":"ZNF384","gene_name":"zinc finger protein 384 [Source:HGNC Symbol;Acc:HGNC:11955]","synonyms":"TNRC1,NP,NMP4,CIZ,CAGH1A","biotype":"protein_coding","ncbi_id":"171017","summary":"This gene encodes a C2H2-type zinc finger protein, which may function as a transcription factor. This gene also contains long CAG trinucleotide repeats that encode consecutive glutamine residues. The protein appears to bind and regulate the promoters of the extracellular matrix genes MMP1, MMP3, MMP7 and COL1A1. Studies in mouse suggest that nuclear matrix transcription factors (NP/NMP4) may be part of a general mechanical pathway that couples cell construction and function during extracellular matrix remodeling. Alternative splicing results in multiple transcript variants. Recurrent rearrangements of this gene with the Ewing's sarcoma gene, EWSR1 on chromosome 22, or with the TAF15 gene on chromosome 17, or with the TCF3 (E2A) gene on chromosome 19, have been observed in acute leukemia. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Apr 2011]","start":6666477,"end":6689572,"strand":-1,"description":"zinc finger protein 384 [Source:HGNC Symbol;Acc:HGNC:11955]"}, {"versioned_ensembl_gene_id":"ENSG00000152705.7","gene_symbol":"CATSPER3","gene_name":"cation channel sperm associated 3 [Source:HGNC Symbol;Acc:HGNC:20819]","synonyms":"CACRC","biotype":"protein_coding","ncbi_id":"347732","summary":null,"start":134967906,"end":135011707,"strand":1,"description":"cation channel sperm associated 3 [Source:HGNC Symbol;Acc:HGNC:20819]"}, {"versioned_ensembl_gene_id":"ENSG00000231213.6","gene_symbol":"PLSCR5","gene_name":"phospholipid scramblase family member 5 [Source:HGNC Symbol;Acc:HGNC:19952]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389158","summary":null,"start":146576555,"end":146606216,"strand":-1,"description":"phospholipid scramblase family member 5 [Source:HGNC Symbol;Acc:HGNC:19952]"}, {"versioned_ensembl_gene_id":"ENSG00000227141.2","gene_symbol":"AL160286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179586705,"end":179589175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119723.16","gene_symbol":"COQ6","gene_name":"coenzyme Q6, monooxygenase [Source:HGNC Symbol;Acc:HGNC:20233]","synonyms":"CGI-10","biotype":"protein_coding","ncbi_id":"51004","summary":"The protein encoded by this gene belongs to the ubiH/COQ6 family. It is an evolutionarily conserved monooxygenase required for the biosynthesis of coenzyme Q10 (or ubiquinone), which is an essential component of the mitochondrial electron transport chain, and one of the most potent lipophilic antioxidants implicated in the protection of cell damage by reactive oxygen species. Knockdown of this gene in mouse and zebrafish results in decreased growth due to increased apoptosis. Mutations in this gene are associated with autosomal recessive coenzyme Q10 deficiency-6 (COQ10D6), which manifests as nephrotic syndrome with sensorineural deafness. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2012]","start":73949926,"end":73963670,"strand":1,"description":"coenzyme Q6, monooxygenase [Source:HGNC Symbol;Acc:HGNC:20233]"}, {"versioned_ensembl_gene_id":"ENSG00000079459.12","gene_symbol":"FDFT1","gene_name":"farnesyl-diphosphate farnesyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3629]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2222","summary":"This gene encodes a membrane-associated enzyme located at a branch point in the mevalonate pathway. The encoded protein is the first specific enzyme in cholesterol biosynthesis, catalyzing the dimerization of two molecules of farnesyl diphosphate in a two-step reaction to form squalene. [provided by RefSeq, Jul 2008]","start":11795573,"end":11839309,"strand":1,"description":"farnesyl-diphosphate farnesyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:3629]"}, {"versioned_ensembl_gene_id":"ENSG00000157554.18","gene_symbol":"ERG","gene_name":"ERG, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3446]","synonyms":"p55,erg-3","biotype":"protein_coding","ncbi_id":"2078","summary":"This gene encodes a member of the erythroblast transformation-specific (ETS) family of transcriptions factors. All members of this family are key regulators of embryonic development, cell proliferation, differentiation, angiogenesis, inflammation, and apoptosis. The protein encoded by this gene is mainly expressed in the nucleus. It contains an ETS DNA-binding domain and a PNT (pointed) domain which is implicated in the self-association of chimeric oncoproteins. This protein is required for platelet adhesion to the subendothelium, inducing vascular cell remodeling. It also regulates hematopoesis, and the differentiation and maturation of megakaryocytic cells. This gene is involved in chromosomal translocations, resulting in different fusion gene products, such as TMPSSR2-ERG and NDRG1-ERG in prostate cancer, EWS-ERG in Ewing's sarcoma and FUS-ERG in acute myeloid leukemia. More than two dozens of transcript variants generated from combinatorial usage of three alternative promoters and multiple alternative splicing events have been reported, but the full-length nature of many of these variants has not been determined. [provided by RefSeq, Apr 2014]","start":38380027,"end":38661780,"strand":-1,"description":"ERG, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3446]"}, {"versioned_ensembl_gene_id":"ENSG00000263958.1","gene_symbol":"AC091138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72868388,"end":72881399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186603.5","gene_symbol":"HPDL","gene_name":"4-hydroxyphenylpyruvate dioxygenase like [Source:HGNC Symbol;Acc:HGNC:28242]","synonyms":"MGC15668,GLOXD1,4-HPPD-L","biotype":"protein_coding","ncbi_id":"84842","summary":"The protein encoded by this intronless gene localizes to mitochondria, where it may function as 4-hydroxyphenylpyruvate dioxygenase. Clinical studies have identified several bi-allelic variants in this gene that lower the level of the encoded protein and lead to a clinically variable form of pediatric-onset spastic movement disorder. [provided by RefSeq, Aug 2020]","start":45326905,"end":45328533,"strand":1,"description":"4-hydroxyphenylpyruvate dioxygenase like [Source:HGNC Symbol;Acc:HGNC:28242]"}, {"versioned_ensembl_gene_id":"ENSG00000235414.3","gene_symbol":"RPSAP24","gene_name":"ribosomal protein SA pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391462","summary":null,"start":174043008,"end":174043880,"strand":1,"description":"ribosomal protein SA pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36362]"}, {"versioned_ensembl_gene_id":"ENSG00000236472.1","gene_symbol":"AC002401.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50135586,"end":50146176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186509.4","gene_symbol":"OR9Q1","gene_name":"olfactory receptor family 9 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:14724]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219956","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58023881,"end":58181616,"strand":1,"description":"olfactory receptor family 9 subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:14724]"}, {"versioned_ensembl_gene_id":"ENSG00000230437.1","gene_symbol":"AL136460.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12305613,"end":12316485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238277.1","gene_symbol":"AC068483.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129063846,"end":129071725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237532.1","gene_symbol":"AC012451.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128580491,"end":128581576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282647.1","gene_symbol":"LINC01070","gene_name":"long intergenic non-protein coding RNA 1070 [Source:HGNC Symbol;Acc:HGNC:49110]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928698","summary":null,"start":112197350,"end":112201000,"strand":1,"description":"long intergenic non-protein coding RNA 1070 [Source:HGNC Symbol;Acc:HGNC:49110]"}, {"versioned_ensembl_gene_id":"ENSG00000233409.1","gene_symbol":"FANK1-AS1","gene_name":"FANK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43915]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410540","summary":null,"start":125972188,"end":125973126,"strand":-1,"description":"FANK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43915]"}, {"versioned_ensembl_gene_id":"ENSG00000236582.1","gene_symbol":"PRPF38AP2","gene_name":"PRP38 domain containing A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131947","summary":null,"start":17577362,"end":17578212,"strand":1,"description":"PRP38 domain containing A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44693]"}, {"versioned_ensembl_gene_id":"ENSG00000259211.1","gene_symbol":"AC013356.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40464193,"end":40466726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148158.16","gene_symbol":"SNX30","gene_name":"sorting nexin family member 30 [Source:HGNC Symbol;Acc:HGNC:23685]","synonyms":"ATG24A","biotype":"protein_coding","ncbi_id":"401548","summary":null,"start":112750838,"end":112881671,"strand":1,"description":"sorting nexin family member 30 [Source:HGNC Symbol;Acc:HGNC:23685]"}, {"versioned_ensembl_gene_id":"ENSG00000255303.2","gene_symbol":"OR5BA1P","gene_name":"olfactory receptor family 5 subfamily BA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15270]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81210","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57861948,"end":57873588,"strand":-1,"description":"olfactory receptor family 5 subfamily BA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15270]"}, {"versioned_ensembl_gene_id":"ENSG00000233900.1","gene_symbol":"RPL17P35","gene_name":"ribosomal protein L17 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271284","summary":null,"start":64620374,"end":64620922,"strand":-1,"description":"ribosomal protein L17 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:35819]"}, {"versioned_ensembl_gene_id":"ENSG00000249199.1","gene_symbol":"AC026785.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17369225,"end":17375577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253213.1","gene_symbol":"AC010306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171251866,"end":171252982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255375.1","gene_symbol":"AL078612.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32132699,"end":32143579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227160.3","gene_symbol":"THEM7P","gene_name":"thioesterase superfamily member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:50386]","synonyms":"RP1-65P5.1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"106480297","summary":null,"start":32112049,"end":32343409,"strand":-1,"description":"thioesterase superfamily member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:50386]"}, {"versioned_ensembl_gene_id":"ENSG00000177197.7","gene_symbol":"PCNPP5","gene_name":"PEST containing nuclear protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507361","summary":null,"start":48328084,"end":48328564,"strand":-1,"description":"PEST containing nuclear protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41977]"}, {"versioned_ensembl_gene_id":"ENSG00000203872.6","gene_symbol":"C6orf163","gene_name":"chromosome 6 open reading frame 163 [Source:HGNC Symbol;Acc:HGNC:21403]","synonyms":null,"biotype":"protein_coding","ncbi_id":"206412","summary":null,"start":87344849,"end":87365463,"strand":1,"description":"chromosome 6 open reading frame 163 [Source:HGNC Symbol;Acc:HGNC:21403]"}, {"versioned_ensembl_gene_id":"ENSG00000259048.1","gene_symbol":"AL392023.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38034287,"end":38194281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196284.15","gene_symbol":"SUPT3H","gene_name":"SPT3 homolog, SAGA and STAGA complex component [Source:HGNC Symbol;Acc:HGNC:11466]","synonyms":"SPT3L,SPT3","biotype":"protein_coding","ncbi_id":"8464","summary":null,"start":44809317,"end":45377953,"strand":-1,"description":"SPT3 homolog, SAGA and STAGA complex component [Source:HGNC Symbol;Acc:HGNC:11466]"}, {"versioned_ensembl_gene_id":"ENSG00000233162.1","gene_symbol":"MORF4L1P6","gene_name":"mortality factor 4 like 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39258]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873878","summary":null,"start":73474563,"end":73474830,"strand":1,"description":"mortality factor 4 like 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39258]"}, {"versioned_ensembl_gene_id":"ENSG00000282365.1","gene_symbol":"LINC02091","gene_name":"long intergenic non-protein coding RNA 2091 [Source:HGNC Symbol;Acc:HGNC:52942]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506371","summary":null,"start":182756,"end":190502,"strand":-1,"description":"long intergenic non-protein coding RNA 2091 [Source:HGNC Symbol;Acc:HGNC:52942]"}, {"versioned_ensembl_gene_id":"ENSG00000131264.3","gene_symbol":"CDX4","gene_name":"caudal type homeobox 4 [Source:HGNC Symbol;Acc:HGNC:1808]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1046","summary":"This gene encodes a member of a small subfamily of homeobox containing transcription factors. The encoded protein may regulate homeobox gene expression during anteroposterior patterning and hematopoiesis. [provided by RefSeq, Aug 2012]","start":73447254,"end":73455245,"strand":1,"description":"caudal type homeobox 4 [Source:HGNC Symbol;Acc:HGNC:1808]"}, {"versioned_ensembl_gene_id":"ENSG00000237041.1","gene_symbol":"AC007679.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206040432,"end":206040845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196411.9","gene_symbol":"EPHB4","gene_name":"EPH receptor B4 [Source:HGNC Symbol;Acc:HGNC:3395]","synonyms":"HTK,Tyro11","biotype":"protein_coding","ncbi_id":"2050","summary":"Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene binds to ephrin-B2 and plays an essential role in vascular development. [provided by RefSeq, Jul 2008]","start":100802565,"end":100827521,"strand":-1,"description":"EPH receptor B4 [Source:HGNC Symbol;Acc:HGNC:3395]"}, {"versioned_ensembl_gene_id":"ENSG00000159579.13","gene_symbol":"RSPRY1","gene_name":"ring finger and SPRY domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29420]","synonyms":"KIAA1972","biotype":"protein_coding","ncbi_id":"89970","summary":"This gene encodes a glycoprotein that contains a RING-type zinc finger domain and an SPRY domain of unknown function. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":57186137,"end":57240475,"strand":1,"description":"ring finger and SPRY domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29420]"}, {"versioned_ensembl_gene_id":"ENSG00000226912.1","gene_symbol":"ISCA2P1","gene_name":"iron-sulfur cluster assembly 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38022]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287193","summary":null,"start":26644889,"end":26645336,"strand":-1,"description":"iron-sulfur cluster assembly 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38022]"}, {"versioned_ensembl_gene_id":"ENSG00000234325.1","gene_symbol":"MRPS10P2","gene_name":"mitochondrial ribosomal protein S10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29727]","synonyms":"MRPS10P4,MRPS10P3","biotype":"processed_pseudogene","ncbi_id":"359802","summary":null,"start":4414580,"end":4414960,"strand":-1,"description":"mitochondrial ribosomal protein S10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29727]"}, {"versioned_ensembl_gene_id":"ENSG00000146282.17","gene_symbol":"RARS2","gene_name":"arginyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21406]","synonyms":"PRO1992,MGC23778,MGC14993,dJ382I10.6,DALRD2,RARSL","biotype":"protein_coding","ncbi_id":"57038","summary":"This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":87514378,"end":87590003,"strand":-1,"description":"arginyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21406]"}, {"versioned_ensembl_gene_id":"ENSG00000226398.1","gene_symbol":"AC013480.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42015625,"end":42025302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281998.1","gene_symbol":"AC025882.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36863468,"end":36938493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149443.7","gene_symbol":"C20orf78","gene_name":"chromosome 20 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:16210]","synonyms":"dJ1068E13.1","biotype":"sense_overlapping","ncbi_id":"100128496","summary":null,"start":18809728,"end":18830153,"strand":-1,"description":"chromosome 20 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:16210]"}, {"versioned_ensembl_gene_id":"ENSG00000204717.4","gene_symbol":"AC073464.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94795808,"end":94806452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237383.1","gene_symbol":"CNN2P11","gene_name":"calponin 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39536]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100689296","summary":null,"start":94725674,"end":94725935,"strand":-1,"description":"calponin 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39536]"}, {"versioned_ensembl_gene_id":"ENSG00000268133.1","gene_symbol":"AC003002.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57363566,"end":57398584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280737.1","gene_symbol":"LINC02549","gene_name":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928280","summary":null,"start":68266500,"end":68342717,"strand":-1,"description":"long intergenic non-protein coding RNA 2549 [Source:HGNC Symbol;Acc:HGNC:53584]"}, {"versioned_ensembl_gene_id":"ENSG00000258562.2","gene_symbol":"AC106028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92762757,"end":92763750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215603.4","gene_symbol":"ZNF92P1Y","gene_name":"zinc finger protein 92 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:39553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419554","summary":null,"start":7853686,"end":7854876,"strand":-1,"description":"zinc finger protein 92 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:39553]"}, {"versioned_ensembl_gene_id":"ENSG00000253447.5","gene_symbol":"AC113423.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174081506,"end":174086559,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176788.8","gene_symbol":"BASP1","gene_name":"brain abundant membrane attached signal protein 1 [Source:HGNC Symbol;Acc:HGNC:957]","synonyms":"NAP22,NAP-22,CAP23,CAP-23","biotype":"protein_coding","ncbi_id":"10409","summary":"This gene encodes a membrane bound protein with several transient phosphorylation sites and PEST motifs. Conservation of proteins with PEST sequences among different species supports their functional significance. PEST sequences typically occur in proteins with high turnover rates. Immunological characteristics of this protein are species specific. This protein also undergoes N-terminal myristoylation. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2012]","start":17065598,"end":17276843,"strand":1,"description":"brain abundant membrane attached signal protein 1 [Source:HGNC Symbol;Acc:HGNC:957]"}, {"versioned_ensembl_gene_id":"ENSG00000224387.1","gene_symbol":"AL139246.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2492300,"end":2493258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213653.4","gene_symbol":"RPL22P22","gene_name":"ribosomal protein L22 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36109]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130922","summary":null,"start":82506434,"end":82506812,"strand":-1,"description":"ribosomal protein L22 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36109]"}, {"versioned_ensembl_gene_id":"ENSG00000279641.1","gene_symbol":"AC120057.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7242200,"end":7243814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267049.1","gene_symbol":"AC002398.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35769144,"end":35771028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249555.2","gene_symbol":"TMEM248P1","gene_name":"transmembrane protein 248 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44053]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645841","summary":null,"start":125723267,"end":125724217,"strand":-1,"description":"transmembrane protein 248 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44053]"}, {"versioned_ensembl_gene_id":"ENSG00000231529.1","gene_symbol":"AC096644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220485104,"end":220487043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204310.12","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32168212,"end":32178096,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000227442.1","gene_symbol":"HLA-DRB2","gene_name":"major histocompatibility complex, class II, DR beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4950]","synonyms":"HLA-DR2B","biotype":"unprocessed_pseudogene","ncbi_id":"3124","summary":null,"start":32488465,"end":32502952,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4950]"}, {"versioned_ensembl_gene_id":"ENSG00000250769.2","gene_symbol":"AC119751.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49507764,"end":49508806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079999.13","gene_symbol":"KEAP1","gene_name":"kelch like ECH associated protein 1 [Source:HGNC Symbol;Acc:HGNC:23177]","synonyms":"MGC9454,MGC4407,MGC20887,MGC1114,MGC10630,KLHL19,KIAA0132,INrf2","biotype":"protein_coding","ncbi_id":"9817","summary":"This gene encodes a protein containing KELCH-1 like domains, as well as a BTB/POZ domain. Kelch-like ECH-associated protein 1 interacts with NF-E2-related factor 2 in a redox-sensitive manner and the dissociation of the proteins in the cytoplasm is followed by transportation of NF-E2-related factor 2 to the nucleus. This interaction results in the expression of the catalytic subunit of gamma-glutamylcysteine synthetase. Two alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":10486120,"end":10503741,"strand":-1,"description":"kelch like ECH associated protein 1 [Source:HGNC Symbol;Acc:HGNC:23177]"}, {"versioned_ensembl_gene_id":"ENSG00000232883.1","gene_symbol":"AL451081.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220316667,"end":220317599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232155.1","gene_symbol":"AC244090.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154605858,"end":154605950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258892.1","gene_symbol":"AL160236.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":60879714,"end":60982585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279555.1","gene_symbol":"AC091181.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57277920,"end":57280017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258797.2","gene_symbol":"AC023310.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20545576,"end":20549444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142615.7","gene_symbol":"CELA2A","gene_name":"chymotrypsin like elastase family member 2A [Source:HGNC Symbol;Acc:HGNC:24609]","synonyms":"ELA2A","biotype":"protein_coding","ncbi_id":"63036","summary":"Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes which encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Like most of the human elastases, elastase 2A is secreted from the pancreas as a zymogen. In other species, elastase 2A has been shown to preferentially cleave proteins after leucine, methionine, and phenylalanine residues. [provided by RefSeq, May 2009]","start":15456728,"end":15472091,"strand":1,"description":"chymotrypsin like elastase family member 2A [Source:HGNC Symbol;Acc:HGNC:24609]"}, {"versioned_ensembl_gene_id":"ENSG00000167173.18","gene_symbol":"C15orf39","gene_name":"chromosome 15 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:24497]","synonyms":"FLJ46337,DKFZP434H132","biotype":"protein_coding","ncbi_id":"56905","summary":null,"start":75195643,"end":75212169,"strand":1,"description":"chromosome 15 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:24497]"}, {"versioned_ensembl_gene_id":"ENSG00000258952.2","gene_symbol":"SALRNA1","gene_name":"senescence associated long non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:49001]","synonyms":"XLOC_023166,SAL-RNA1","biotype":"lincRNA","ncbi_id":"104548971","summary":null,"start":60639216,"end":60642589,"strand":1,"description":"senescence associated long non-coding RNA 1 [Source:HGNC Symbol;Acc:HGNC:49001]"}, {"versioned_ensembl_gene_id":"ENSG00000171045.14","gene_symbol":"TSNARE1","gene_name":"t-SNARE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26437]","synonyms":"FLJ31164","biotype":"protein_coding","ncbi_id":"203062","summary":null,"start":142212080,"end":142403240,"strand":-1,"description":"t-SNARE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26437]"}, {"versioned_ensembl_gene_id":"ENSG00000172156.3","gene_symbol":"CCL11","gene_name":"C-C motif chemokine ligand 11 [Source:HGNC Symbol;Acc:HGNC:10610]","synonyms":"MGC22554,eotaxin,SCYA11","biotype":"protein_coding","ncbi_id":"6356","summary":"This antimicrobial gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, displays chemotactic activity for eosinophils, but not mononuclear cells or neutrophils. This eosinophil-specific chemokine is thought to be involved in eosinophilic inflammatory diseases such as atopic dermatitis, allergic rhinitis, asthma and parasitic infections. [provided by RefSeq, Sep 2014]","start":34285668,"end":34288334,"strand":1,"description":"C-C motif chemokine ligand 11 [Source:HGNC Symbol;Acc:HGNC:10610]"}, {"versioned_ensembl_gene_id":"ENSG00000272769.1","gene_symbol":"AC097532.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132345616,"end":132347297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164930.11","gene_symbol":"FZD6","gene_name":"frizzled class receptor 6 [Source:HGNC Symbol;Acc:HGNC:4044]","synonyms":"Hfz6","biotype":"protein_coding","ncbi_id":"8323","summary":"This gene represents a member of the 'frizzled' gene family, which encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The protein encoded by this family member contains a signal peptide, a cysteine-rich domain in the N-terminal extracellular region, and seven transmembrane domains, but unlike other family members, this protein does not contain a C-terminal PDZ domain-binding motif. This protein functions as a negative regulator of the canonical Wnt/beta-catenin signaling cascade, thereby inhibiting the processes that trigger oncogenic transformation, cell proliferation, and inhibition of apoptosis. Alternative splicing results in multiple transcript variants, some of which do not encode a protein with a predicted signal peptide.[provided by RefSeq, Aug 2011]","start":103298433,"end":103332866,"strand":1,"description":"frizzled class receptor 6 [Source:HGNC Symbol;Acc:HGNC:4044]"}, {"versioned_ensembl_gene_id":"ENSG00000241668.2","gene_symbol":"RPL19P11","gene_name":"ribosomal protein L19 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36953]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270950","summary":null,"start":31053565,"end":31054153,"strand":1,"description":"ribosomal protein L19 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36953]"}, {"versioned_ensembl_gene_id":"ENSG00000254487.2","gene_symbol":"AC130364.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49817778,"end":49825553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198759.11","gene_symbol":"EGFL6","gene_name":"EGF like domain multiple 6 [Source:HGNC Symbol;Acc:HGNC:3235]","synonyms":"MAEG","biotype":"protein_coding","ncbi_id":"25975","summary":"This gene encodes a member of the epidermal growth factor (EGF) repeat superfamily. Members of this superfamily are characterized by the presence of EGF-like repeats and are often involved in the regulation of cell cycle, proliferation, and developmental processes. The gene product contains a signal peptide, suggesting that it is secreted; an EGF repeat region consisting of 4 complete EGF-like repeats and 1 partial EGF-like repeat, 3 of which have a calcium-binding consensus sequence; an arg-gly-asp integrin association motif; and a MAM domain, which is believed to have an adhesive function. This gene is expressed early during development, and its expression has been detected in lung and meningioma tumors. [provided by RefSeq, Jul 2008]","start":13569605,"end":13633575,"strand":1,"description":"EGF like domain multiple 6 [Source:HGNC Symbol;Acc:HGNC:3235]"}, {"versioned_ensembl_gene_id":"ENSG00000278624.2","gene_symbol":"AZU1","gene_name":"azurocidin 1 [Source:HGNC Symbol;Acc:HGNC:913]","synonyms":"CAP37,AZU,AZAMP,NAZC,HUMAZUR,HBP","biotype":"protein_coding","ncbi_id":"566","summary":"Azurophil granules, specialized lysosomes of the neutrophil, contain at least 10 proteins implicated in the killing of microorganisms. This gene encodes a preproprotein that is proteolytically processed to generate a mature azurophil granule antibiotic protein, with monocyte chemotactic and antimicrobial activity. It is also an important multifunctional inflammatory mediator. This encoded protein is a member of the serine protease gene family but it is not a serine proteinase, because the active site serine and histidine residues are replaced. The genes encoding this protein, neutrophil elastase 2, and proteinase 3 are in a cluster located at chromosome 19pter. All 3 genes are expressed coordinately and their protein products are packaged together into azurophil granules during neutrophil differentiation. [provided by RefSeq, Nov 2015]","start":825097,"end":832018,"strand":1,"description":"azurocidin 1 [Source:HGNC Symbol;Acc:HGNC:913]"}, {"versioned_ensembl_gene_id":"ENSG00000233357.2","gene_symbol":"RPL30P15","gene_name":"ribosomal protein L30 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271192","summary":null,"start":13574746,"end":13575066,"strand":1,"description":"ribosomal protein L30 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36542]"}, {"versioned_ensembl_gene_id":"ENSG00000271284.1","gene_symbol":"SMIM12P1","gene_name":"small integral membrane protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288503","summary":null,"start":108423612,"end":108423885,"strand":1,"description":"small integral membrane protein 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51598]"}, {"versioned_ensembl_gene_id":"ENSG00000263089.1","gene_symbol":"AC007114.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57092145,"end":57096425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228764.1","gene_symbol":"ZNF885P","gene_name":"zinc finger protein 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:38456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419734","summary":null,"start":20390051,"end":20396796,"strand":1,"description":"zinc finger protein 885, pseudogene [Source:HGNC Symbol;Acc:HGNC:38456]"}, {"versioned_ensembl_gene_id":"ENSG00000105185.11","gene_symbol":"PDCD5","gene_name":"programmed cell death 5 [Source:HGNC Symbol;Acc:HGNC:8764]","synonyms":"MGC9294,TFAR19","biotype":"protein_coding","ncbi_id":"9141","summary":"This gene encodes a protein that is upregulated during apoptosis where it translocates rapidly from the cytoplasm to the nucleus. The encoded protein may be an important regulator of K(lysine) acetyltransferase 5 (a protein involved in transcription, DNA damage response and cell cycle control) by inhibiting its proteasome-dependent degradation. Pseudogenes have been identified on chromosomes 5 and 12 [provided by RefSeq, Dec 2010]","start":32581068,"end":32587452,"strand":1,"description":"programmed cell death 5 [Source:HGNC Symbol;Acc:HGNC:8764]"}, {"versioned_ensembl_gene_id":"ENSG00000186103.3","gene_symbol":"ARGFX","gene_name":"arginine-fifty homeobox [Source:HGNC Symbol;Acc:HGNC:30146]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503582","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the ARGFX homeobox gene family. [provided by RefSeq, Jul 2008]","start":121570704,"end":121586634,"strand":1,"description":"arginine-fifty homeobox [Source:HGNC Symbol;Acc:HGNC:30146]"}, {"versioned_ensembl_gene_id":"ENSG00000240005.5","gene_symbol":"AC106047.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26859806,"end":26860599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254212.1","gene_symbol":"AC009901.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84864668,"end":84864907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104341.16","gene_symbol":"LAPTM4B","gene_name":"lysosomal protein transmembrane 4 beta [Source:HGNC Symbol;Acc:HGNC:13646]","synonyms":"LC27","biotype":"protein_coding","ncbi_id":"55353","summary":null,"start":97775057,"end":97853013,"strand":1,"description":"lysosomal protein transmembrane 4 beta [Source:HGNC Symbol;Acc:HGNC:13646]"}, {"versioned_ensembl_gene_id":"ENSG00000177182.10","gene_symbol":"CLVS1","gene_name":"clavesin 1 [Source:HGNC Symbol;Acc:HGNC:23139]","synonyms":"RLBP1L1,MGC34646,CRALBPL,C6orf212L","biotype":"protein_coding","ncbi_id":"157807","summary":null,"start":61057158,"end":61501645,"strand":1,"description":"clavesin 1 [Source:HGNC Symbol;Acc:HGNC:23139]"}, {"versioned_ensembl_gene_id":"ENSG00000275754.2","gene_symbol":"OR2T2","gene_name":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]","synonyms":"OR2T2P","biotype":"protein_coding","ncbi_id":"401992","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248455242,"end":248456216,"strand":1,"description":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]"}, {"versioned_ensembl_gene_id":"ENSG00000028277.21","gene_symbol":"POU2F2","gene_name":"POU class 2 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9213]","synonyms":"OTF2,OCT2","biotype":"protein_coding","ncbi_id":"5452","summary":"The protein encoded by this gene is a homeobox-containing transcription factor of the POU domain family. The encoded protein binds the octamer sequence 5'-ATTTGCAT-3', a common transcription factor binding site in immunoglobulin gene promoters. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":42086110,"end":42196585,"strand":-1,"description":"POU class 2 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9213]"}, {"versioned_ensembl_gene_id":"ENSG00000155508.13","gene_symbol":"CNOT8","gene_name":"CCR4-NOT transcription complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:9207]","synonyms":"POP2,hCAF1,CALIF,CAF1","biotype":"protein_coding","ncbi_id":"9337","summary":null,"start":154857553,"end":154876793,"strand":1,"description":"CCR4-NOT transcription complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:9207]"}, {"versioned_ensembl_gene_id":"ENSG00000255481.2","gene_symbol":"OR56A7P","gene_name":"olfactory receptor family 56 subfamily A member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15244]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81236","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6045807,"end":6046747,"strand":-1,"description":"olfactory receptor family 56 subfamily A member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:15244]"}, {"versioned_ensembl_gene_id":"ENSG00000225407.3","gene_symbol":"AC025188.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76691439,"end":76716215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250574.1","gene_symbol":"AC112173.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76510440,"end":76510766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229282.1","gene_symbol":"AL031963.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3055890,"end":3056761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274670.1","gene_symbol":"AC137590.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132083540,"end":132083779,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250282.1","gene_symbol":"AC002401.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50100704,"end":50101920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090376.10","gene_symbol":"IRAK3","gene_name":"interleukin 1 receptor associated kinase 3 [Source:HGNC Symbol;Acc:HGNC:17020]","synonyms":"IRAK-M","biotype":"protein_coding","ncbi_id":"11213","summary":"This gene encodes a member of the interleukin-1 receptor-associated kinase protein family. Members of this family are essential components of the Toll/IL-R immune signal transduction pathways. This protein is primarily expressed in monocytes and macrophages and functions as a negative regulator of Toll-like receptor signaling. Mutations in this gene are associated with a susceptibility to asthma. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":66188879,"end":66254622,"strand":1,"description":"interleukin 1 receptor associated kinase 3 [Source:HGNC Symbol;Acc:HGNC:17020]"}, {"versioned_ensembl_gene_id":"ENSG00000235535.7","gene_symbol":"AL445259.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123389421,"end":123510241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258739.1","gene_symbol":"ENO1P2","gene_name":"enolase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37943]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100419098","summary":null,"start":92420860,"end":92422735,"strand":1,"description":"enolase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37943]"}, {"versioned_ensembl_gene_id":"ENSG00000231763.1","gene_symbol":"PQLC1P1","gene_name":"PQ loop repeat containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43986]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479032","summary":null,"start":88610241,"end":88610669,"strand":-1,"description":"PQ loop repeat containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43986]"}, {"versioned_ensembl_gene_id":"ENSG00000164220.6","gene_symbol":"F2RL2","gene_name":"coagulation factor II thrombin receptor like 2 [Source:HGNC Symbol;Acc:HGNC:3539]","synonyms":"PAR3","biotype":"protein_coding","ncbi_id":"2151","summary":"This gene encodes a member of the protease-activated receptor (PAR) family which is a subfamily of the seven transmembrane G protein-coupled cell surface receptor family. The encoded protein acts as a cofactor in the thrombin-mediated cleavage and activation of the protease-activated receptor family member PAR4. The encoded protein plays an essential role in hemostasis and thrombosis. Alternate splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Feb 2012]","start":76615482,"end":76623434,"strand":-1,"description":"coagulation factor II thrombin receptor like 2 [Source:HGNC Symbol;Acc:HGNC:3539]"}, {"versioned_ensembl_gene_id":"ENSG00000140557.11","gene_symbol":"ST8SIA2","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10870]","synonyms":"STX,ST8SIA-II,SIAT8B,HsT19690","biotype":"protein_coding","ncbi_id":"8128","summary":"The protein encoded by this gene is a type II membrane protein that is thought to catalyze the transfer of sialic acid from CMP-sialic acid to N-linked oligosaccharides and glycoproteins. The encoded protein may be found in the Golgi apparatus and may be involved in the production of polysialic acid, a modulator of the adhesive properties of neural cell adhesion molecule (NCAM1). This protein is a member of glycosyltransferase family 29. [provided by RefSeq, Jul 2008]","start":92393828,"end":92468728,"strand":1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10870]"}, {"versioned_ensembl_gene_id":"ENSG00000237709.1","gene_symbol":"EEF1A1P28","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:37902]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442709","summary":null,"start":88639014,"end":88640416,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:37902]"}, {"versioned_ensembl_gene_id":"ENSG00000233579.1","gene_symbol":"KRT8P15","gene_name":"keratin 8 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:33367]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645834","summary":null,"start":202840331,"end":202841781,"strand":-1,"description":"keratin 8 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:33367]"}, {"versioned_ensembl_gene_id":"ENSG00000240761.1","gene_symbol":"AC098831.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202773720,"end":202774360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282024.1","gene_symbol":"AL009031.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16259101,"end":16264553,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137198.9","gene_symbol":"GMPR","gene_name":"guanosine monophosphate reductase [Source:HGNC Symbol;Acc:HGNC:4376]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2766","summary":"This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. The protein also functions in the re-utilization of free intracellular bases and purine nucleosides.[provided by RefSeq, Oct 2009]","start":16238580,"end":16295549,"strand":1,"description":"guanosine monophosphate reductase [Source:HGNC Symbol;Acc:HGNC:4376]"}, {"versioned_ensembl_gene_id":"ENSG00000229020.4","gene_symbol":"AKR7A2P1","gene_name":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]","synonyms":"AFARP1","biotype":"processed_pseudogene","ncbi_id":"246182","summary":null,"start":112923423,"end":112924337,"strand":1,"description":"aldo-keto reductase family 7 member A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24062]"}, {"versioned_ensembl_gene_id":"ENSG00000238198.1","gene_symbol":"AL357055.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113011687,"end":113073105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178980.14","gene_symbol":"SELENOW","gene_name":"selenoprotein W [Source:HGNC Symbol;Acc:HGNC:10752]","synonyms":"SEPW1,SELW","biotype":"protein_coding","ncbi_id":"6415","summary":"This gene encodes a selenoprotein containing a selenocysteine (Sec) residue, which is encoded by the UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is highly expressed in skeletal muscle, heart and brain. It belongs to the SelWTH family, which possesses a thioredoxin-like fold and a conserved CxxU (C is cysteine, U is Sec) motif, suggesting a redox function for this gene. Studies in mouse show that this selenoprotein is involved in muscle growth and differentiation, and in the protection of neurons from oxidative stress during neuronal development. A retroprocessed pseudogene of this locus has been identified on chromosome 1. [provided by RefSeq, Aug 2017]","start":47778572,"end":47784686,"strand":1,"description":"selenoprotein W [Source:HGNC Symbol;Acc:HGNC:10752]"}, {"versioned_ensembl_gene_id":"ENSG00000243431.1","gene_symbol":"RPL5P30","gene_name":"ribosomal protein L5 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35837]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645160","summary":null,"start":118560690,"end":118561580,"strand":1,"description":"ribosomal protein L5 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35837]"}, {"versioned_ensembl_gene_id":"ENSG00000182118.7","gene_symbol":"FAM89A","gene_name":"family with sequence similarity 89 member A [Source:HGNC Symbol;Acc:HGNC:25057]","synonyms":"MGC15887,C1orf153","biotype":"protein_coding","ncbi_id":"375061","summary":null,"start":231018958,"end":231040246,"strand":-1,"description":"family with sequence similarity 89 member A [Source:HGNC Symbol;Acc:HGNC:25057]"}, {"versioned_ensembl_gene_id":"ENSG00000248936.1","gene_symbol":"AC027607.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37588087,"end":37588875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250256.1","gene_symbol":"AC108112.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174618164,"end":174625775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104974.11","gene_symbol":"LILRA1","gene_name":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]","synonyms":"LIR6,LIR-6,CD85i","biotype":"protein_coding","ncbi_id":"11024","summary":"This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":54593582,"end":54602090,"strand":1,"description":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]"}, {"versioned_ensembl_gene_id":"ENSG00000073598.5","gene_symbol":"FNDC8","gene_name":"fibronectin type III domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25286]","synonyms":"DKFZp434H2215","biotype":"protein_coding","ncbi_id":"54752","summary":null,"start":35121579,"end":35130732,"strand":1,"description":"fibronectin type III domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25286]"}, {"versioned_ensembl_gene_id":"ENSG00000188997.7","gene_symbol":"KCTD21","gene_name":"potassium channel tetramerization domain containing 21 [Source:HGNC Symbol;Acc:HGNC:27452]","synonyms":"KCASH2","biotype":"protein_coding","ncbi_id":"283219","summary":null,"start":78171249,"end":78188822,"strand":-1,"description":"potassium channel tetramerization domain containing 21 [Source:HGNC Symbol;Acc:HGNC:27452]"}, {"versioned_ensembl_gene_id":"ENSG00000174145.7","gene_symbol":"NWD2","gene_name":"NACHT and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29229]","synonyms":"KIAA1239","biotype":"protein_coding","ncbi_id":"57495","summary":null,"start":37244220,"end":37449465,"strand":1,"description":"NACHT and WD repeat domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29229]"}, {"versioned_ensembl_gene_id":"ENSG00000244641.2","gene_symbol":"AP000926.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123049787,"end":123050353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254138.1","gene_symbol":"AC113386.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31093977,"end":31267610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104112.8","gene_symbol":"SCG3","gene_name":"secretogranin III [Source:HGNC Symbol;Acc:HGNC:13707]","synonyms":"SgIII,FLJ90833","biotype":"protein_coding","ncbi_id":"29106","summary":"The protein encoded by this gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. Granins may serve as precursors for biologically active peptides. Some granins have been shown to function as helper proteins in sorting and proteolytic processing of prohormones; however, the function of this protein is unknown. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":51681353,"end":51721031,"strand":1,"description":"secretogranin III [Source:HGNC Symbol;Acc:HGNC:13707]"}, {"versioned_ensembl_gene_id":"ENSG00000126259.19","gene_symbol":"KIRREL2","gene_name":"kirre like nephrin family adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:18816]","synonyms":"NLG1,NEPH3,MGC15718,FILTRIN,DKFZp564A1164","biotype":"protein_coding","ncbi_id":"84063","summary":"This gene encodes a type I transmembrane protein and member of the immunoglobulin superfamily of cell adhesion molecules. The encoded protein localizes to adherens junctions in pancreatic beta cells and regulates insulin secretion. Autoantibodies against the encoded protein have been detected in serum from patients with type 1 diabetes. This gene may also play a role in glomerular development and decreased expression of this gene has been observed in human glomerular diseases. This gene and the related opposite-strand gene nephrin (GeneID: 527362) are regulated by a bidirectional promoter. [provided by RefSeq, Jul 2016]","start":35855861,"end":35867109,"strand":1,"description":"kirre like nephrin family adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:18816]"}, {"versioned_ensembl_gene_id":"ENSG00000233827.2","gene_symbol":"FAM58BP","gene_name":"family with sequence similarity 58 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:27373]","synonyms":"FAM58B","biotype":"processed_pseudogene","ncbi_id":"339521","summary":null,"start":200213678,"end":200214322,"strand":1,"description":"family with sequence similarity 58 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:27373]"}, {"versioned_ensembl_gene_id":"ENSG00000259296.1","gene_symbol":"AC020892.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51707995,"end":51715220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233803.9","gene_symbol":"TSPY4","gene_name":"testis specific protein, Y-linked 4 [Source:HGNC Symbol;Acc:HGNC:37287]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728395","summary":null,"start":9337464,"end":9340284,"strand":1,"description":"testis specific protein, Y-linked 4 [Source:HGNC Symbol;Acc:HGNC:37287]"}, {"versioned_ensembl_gene_id":"ENSG00000240875.5","gene_symbol":"LINC00886","gene_name":"long intergenic non-protein coding RNA 886 [Source:HGNC Symbol;Acc:HGNC:48572]","synonyms":null,"biotype":"lincRNA","ncbi_id":"730091","summary":null,"start":156747346,"end":156817062,"strand":-1,"description":"long intergenic non-protein coding RNA 886 [Source:HGNC Symbol;Acc:HGNC:48572]"}, {"versioned_ensembl_gene_id":"ENSG00000257495.5","gene_symbol":"KRT73-AS1","gene_name":"KRT73 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49607]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100127967","summary":null,"start":52601467,"end":52615305,"strand":1,"description":"KRT73 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49607]"}, {"versioned_ensembl_gene_id":"ENSG00000237719.1","gene_symbol":"Z95152.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36091991,"end":36092646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260589.1","gene_symbol":"STAM-AS1","gene_name":"STAM antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49568]","synonyms":"locus3182","biotype":"antisense_RNA","ncbi_id":"102723166","summary":null,"start":17641284,"end":17643878,"strand":-1,"description":"STAM antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49568]"}, {"versioned_ensembl_gene_id":"ENSG00000214402.6","gene_symbol":"LCNL1","gene_name":"lipocalin like 1 [Source:HGNC Symbol;Acc:HGNC:34436]","synonyms":"FLJ45224","biotype":"protein_coding","ncbi_id":"401562","summary":null,"start":136981904,"end":136986410,"strand":1,"description":"lipocalin like 1 [Source:HGNC Symbol;Acc:HGNC:34436]"}, {"versioned_ensembl_gene_id":"ENSG00000100918.12","gene_symbol":"REC8","gene_name":"REC8 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:16879]","synonyms":"Rec8p,REC8L1,kleisin-alpha","biotype":"protein_coding","ncbi_id":"9985","summary":"This gene encodes a member of the kleisin family of SMC (structural maintenance of chromosome) protein partners. The protein localizes to the axial elements of chromosomes during meiosis in both oocytes and spermatocytes. In the mouse, the homologous protein is a key component of the meiotic cohesion complex, which regulates sister chromatid cohesion and recombination between homologous chromosomes. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]","start":24171853,"end":24180257,"strand":1,"description":"REC8 meiotic recombination protein [Source:HGNC Symbol;Acc:HGNC:16879]"}, {"versioned_ensembl_gene_id":"ENSG00000272899.3","gene_symbol":"AC025594.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":128866308,"end":128872044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259536.5","gene_symbol":"AC091045.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40488041,"end":40558019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275841.4","gene_symbol":"LILRA3","gene_name":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]","synonyms":"ILT6,HM43,HM31,LIR4,CD85e,LIR-4","biotype":"protein_coding","ncbi_id":"11026","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]","start":54294391,"end":54301485,"strand":-1,"description":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]"}, {"versioned_ensembl_gene_id":"ENSG00000205035.8","gene_symbol":"AC136759.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49558546,"end":49810419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250674.1","gene_symbol":"AC136628.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179455415,"end":179456095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233058.1","gene_symbol":"LINC00884","gene_name":"long intergenic non-protein coding RNA 884 [Source:HGNC Symbol;Acc:HGNC:48570]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"401106","summary":null,"start":194487454,"end":194518279,"strand":1,"description":"long intergenic non-protein coding RNA 884 [Source:HGNC Symbol;Acc:HGNC:48570]"}, {"versioned_ensembl_gene_id":"ENSG00000253617.2","gene_symbol":"AC109479.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179385819,"end":179385992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116833.13","gene_symbol":"NR5A2","gene_name":"nuclear receptor subfamily 5 group A member 2 [Source:HGNC Symbol;Acc:HGNC:7984]","synonyms":"LRH-1,hB1F-2,hB1F,FTZ-F1beta,FTZ-F1,FTF,B1F2","biotype":"protein_coding","ncbi_id":"2494","summary":"The protein encoded by this gene is a DNA-binding zinc finger transcription factor and is a member of the fushi tarazu factor-1 subfamily of orphan nuclear receptors. The encoded protein is involved in the expression of genes for hepatitis B virus and cholesterol biosynthesis, and may be an important regulator of embryonic development. [provided by RefSeq, Jun 2016]","start":200027602,"end":200177424,"strand":1,"description":"nuclear receptor subfamily 5 group A member 2 [Source:HGNC Symbol;Acc:HGNC:7984]"}, {"versioned_ensembl_gene_id":"ENSG00000253979.1","gene_symbol":"AC109479.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179377505,"end":179378865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229248.1","gene_symbol":"AC104961.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25016434,"end":25017204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264345.1","gene_symbol":"LINC01894","gene_name":"long intergenic non-protein coding RNA 1894 [Source:HGNC Symbol;Acc:HGNC:52713]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372030","summary":null,"start":24933487,"end":24987682,"strand":-1,"description":"long intergenic non-protein coding RNA 1894 [Source:HGNC Symbol;Acc:HGNC:52713]"}, {"versioned_ensembl_gene_id":"ENSG00000232808.1","gene_symbol":"TTTY20","gene_name":"testis-specific transcript, Y-linked 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18844]","synonyms":"NCRNA00145","biotype":"antisense_RNA","ncbi_id":"252951","summary":null,"start":9329880,"end":9334832,"strand":-1,"description":"testis-specific transcript, Y-linked 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18844]"}, {"versioned_ensembl_gene_id":"ENSG00000279446.1","gene_symbol":"AC005915.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127073587,"end":127075604,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214743.4","gene_symbol":"MRPS5P3","gene_name":"mitochondrial ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29778]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"133615","summary":null,"start":127143082,"end":127143247,"strand":-1,"description":"mitochondrial ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29778]"}, {"versioned_ensembl_gene_id":"ENSG00000275591.4","gene_symbol":"XKR5","gene_name":"XK related 5 [Source:HGNC Symbol;Acc:HGNC:20782]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389610","summary":null,"start":6808517,"end":6835644,"strand":-1,"description":"XK related 5 [Source:HGNC Symbol;Acc:HGNC:20782]"}, {"versioned_ensembl_gene_id":"ENSG00000224159.1","gene_symbol":"HMGB1P9","gene_name":"high mobility group box 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:13320]","synonyms":"HMGB1L9,HMG1L9","biotype":"processed_pseudogene","ncbi_id":"654503","summary":null,"start":218200434,"end":218201388,"strand":1,"description":"high mobility group box 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:13320]"}, {"versioned_ensembl_gene_id":"ENSG00000223948.1","gene_symbol":"AC092648.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67769629,"end":67770468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185864.16","gene_symbol":"NPIPB4","gene_name":"nuclear pore complex interacting protein family member B4 [Source:HGNC Symbol;Acc:HGNC:41985]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440345","summary":null,"start":21834569,"end":21880827,"strand":-1,"description":"nuclear pore complex interacting protein family member B4 [Source:HGNC Symbol;Acc:HGNC:41985]"}, {"versioned_ensembl_gene_id":"ENSG00000254312.1","gene_symbol":"MRPL57P7","gene_name":"mitochondrial ribosomal protein L57 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:29690]","synonyms":"MRP63P7","biotype":"processed_pseudogene","ncbi_id":"359731","summary":null,"start":98906260,"end":98906517,"strand":-1,"description":"mitochondrial ribosomal protein L57 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:29690]"}, {"versioned_ensembl_gene_id":"ENSG00000230487.7","gene_symbol":"PSMG3-AS1","gene_name":"PSMG3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:22230]","synonyms":"KIAA1908","biotype":"lincRNA","ncbi_id":"114796","summary":null,"start":1570073,"end":1589626,"strand":1,"description":"PSMG3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:22230]"}, {"versioned_ensembl_gene_id":"ENSG00000185710.9","gene_symbol":"SMG1P4","gene_name":"SMG1P4, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49861]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100507526","summary":null,"start":21879338,"end":21919156,"strand":-1,"description":"SMG1P4, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49861]"}, {"versioned_ensembl_gene_id":"ENSG00000250846.6","gene_symbol":"EPHA5-AS1","gene_name":"EPHA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50602]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100144602","summary":null,"start":65669961,"end":65698029,"strand":1,"description":"EPHA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50602]"}, {"versioned_ensembl_gene_id":"ENSG00000267555.1","gene_symbol":"AC008805.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32831295,"end":32833168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099949.18","gene_symbol":"LZTR1","gene_name":"leucine zipper like transcription regulator 1 [Source:HGNC Symbol;Acc:HGNC:6742]","synonyms":"LZTR-1,BTBD29","biotype":"protein_coding","ncbi_id":"8216","summary":"This gene encodes a member of the BTB-kelch superfamily. Initially described as a putative transcriptional regulator based on weak homology to members of the basic leucine zipper-like family, the encoded protein subsequently has been shown to localize exclusively to the Golgi network where it may help stabilize the Gogli complex. Deletion of this gene may be associated with DiGeorge syndrome. [provided by RefSeq, Jul 2008]","start":20979462,"end":20999038,"strand":1,"description":"leucine zipper like transcription regulator 1 [Source:HGNC Symbol;Acc:HGNC:6742]"}, {"versioned_ensembl_gene_id":"ENSG00000248817.1","gene_symbol":"PMPCAP1","gene_name":"peptidase, mitochondrial processing alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51348]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"133083","summary":null,"start":92182477,"end":92184052,"strand":-1,"description":"peptidase, mitochondrial processing alpha subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51348]"}, {"versioned_ensembl_gene_id":"ENSG00000264404.2","gene_symbol":"BX547991.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47588681,"end":47599830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244193.1","gene_symbol":"AC008040.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":169945987,"end":169946754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113966.9","gene_symbol":"ARL6","gene_name":"ADP ribosylation factor like GTPase 6 [Source:HGNC Symbol;Acc:HGNC:13210]","synonyms":"RP55,BBS3","biotype":"protein_coding","ncbi_id":"84100","summary":"The protein encoded by this gene belongs to the ARF-like (ADP ribosylation factor-like) sub-family of the ARF family of GTP-binding proteins which are involved in regulation of intracellular traffic. Mutations in this gene are associated with Bardet-Biedl syndrome (BBS). A vision-specific transcript, encoding long isoform BBS3L, has been described (PMID: 20333246). [provided by RefSeq, Apr 2016]","start":97764521,"end":97801242,"strand":1,"description":"ADP ribosylation factor like GTPase 6 [Source:HGNC Symbol;Acc:HGNC:13210]"}, {"versioned_ensembl_gene_id":"ENSG00000107882.11","gene_symbol":"SUFU","gene_name":"SUFU negative regulator of hedgehog signaling [Source:HGNC Symbol;Acc:HGNC:16466]","synonyms":"SUFUH,PRO1280,SUFUXL","biotype":"protein_coding","ncbi_id":"51684","summary":"The Hedgehog signaling pathway plays an important role in early human development. The pathway is a signaling cascade that plays a role in pattern formation and cellular proliferation during development. This gene encodes a negative regulator of the hedgehog signaling pathway. Defects in this gene are a cause of medulloblastoma. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":102503987,"end":102633535,"strand":1,"description":"SUFU negative regulator of hedgehog signaling [Source:HGNC Symbol;Acc:HGNC:16466]"}, {"versioned_ensembl_gene_id":"ENSG00000261729.1","gene_symbol":"AL133383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":185655002,"end":185657168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248259.1","gene_symbol":"MTND4LP31","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52171]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075296","summary":null,"start":64610616,"end":64610909,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52171]"}, {"versioned_ensembl_gene_id":"ENSG00000226732.1","gene_symbol":"ZDHHC20P2","gene_name":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]","synonyms":"OTTHUMG00000133740","biotype":"processed_pseudogene","ncbi_id":"100048908","summary":null,"start":31423425,"end":31423853,"strand":1,"description":"zinc finger DHHC-type containing 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33457]"}, {"versioned_ensembl_gene_id":"ENSG00000275562.1","gene_symbol":"AC104763.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60256720,"end":60258411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213291.3","gene_symbol":"AC010099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125300504,"end":125300878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253959.1","gene_symbol":"LINC01863","gene_name":"long intergenic non-protein coding RNA 1863 [Source:HGNC Symbol;Acc:HGNC:52682]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986480","summary":null,"start":173642519,"end":173658194,"strand":1,"description":"long intergenic non-protein coding RNA 1863 [Source:HGNC Symbol;Acc:HGNC:52682]"}, {"versioned_ensembl_gene_id":"ENSG00000281947.1","gene_symbol":"IGHEP1","gene_name":"immunoglobulin heavy constant epsilon P1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5523]","synonyms":null,"biotype":"IG_C_pseudogene","ncbi_id":"3498","summary":null,"start":105722565,"end":105723298,"strand":-1,"description":"immunoglobulin heavy constant epsilon P1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5523]"}, {"versioned_ensembl_gene_id":"ENSG00000214279.13","gene_symbol":"SCART1","gene_name":"scavenger receptor family member expressed on T-cells 1 [Source:HGNC Symbol;Acc:HGNC:32411]","synonyms":"CD163c-alpha","biotype":"protein_coding","ncbi_id":"619207","summary":null,"start":133453928,"end":133523558,"strand":1,"description":"scavenger receptor family member expressed on T-cells 1 [Source:HGNC Symbol;Acc:HGNC:32411]"}, {"versioned_ensembl_gene_id":"ENSG00000171314.8","gene_symbol":"PGAM1","gene_name":"phosphoglycerate mutase 1 [Source:HGNC Symbol;Acc:HGNC:8888]","synonyms":"PGAMA,PGAM-B","biotype":"protein_coding","ncbi_id":"5223","summary":"The protein encoded by this gene is a mutase that catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":97426160,"end":97433441,"strand":1,"description":"phosphoglycerate mutase 1 [Source:HGNC Symbol;Acc:HGNC:8888]"}, {"versioned_ensembl_gene_id":"ENSG00000167914.11","gene_symbol":"GSDMA","gene_name":"gasdermin A [Source:HGNC Symbol;Acc:HGNC:13311]","synonyms":"GSDM,FLJ39120,GSDM1","biotype":"protein_coding","ncbi_id":"284110","summary":null,"start":39953263,"end":39977766,"strand":1,"description":"gasdermin A [Source:HGNC Symbol;Acc:HGNC:13311]"}, {"versioned_ensembl_gene_id":"ENSG00000282633.1","gene_symbol":"IGHA1","gene_name":"immunoglobulin heavy constant alpha 1 [Source:HGNC Symbol;Acc:HGNC:5478]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3493","summary":null,"start":105707889,"end":105709436,"strand":-1,"description":"immunoglobulin heavy constant alpha 1 [Source:HGNC Symbol;Acc:HGNC:5478]"}, {"versioned_ensembl_gene_id":"ENSG00000258202.1","gene_symbol":"AC026371.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30454919,"end":30492302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100591.7","gene_symbol":"AHSA1","gene_name":"activator of HSP90 ATPase activity 1 [Source:HGNC Symbol;Acc:HGNC:1189]","synonyms":"p38,C14orf3,hAha1,Aha1","biotype":"protein_coding","ncbi_id":"10598","summary":null,"start":77457870,"end":77469474,"strand":1,"description":"activator of HSP90 ATPase activity 1 [Source:HGNC Symbol;Acc:HGNC:1189]"}, {"versioned_ensembl_gene_id":"ENSG00000268714.4","gene_symbol":"ARL14EPL","gene_name":"ADP ribosylation factor like GTPase 14 effector protein like [Source:HGNC Symbol;Acc:HGNC:44201]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644100","summary":null,"start":116022391,"end":116059130,"strand":1,"description":"ADP ribosylation factor like GTPase 14 effector protein like [Source:HGNC Symbol;Acc:HGNC:44201]"}, {"versioned_ensembl_gene_id":"ENSG00000257932.1","gene_symbol":"AC078776.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30320834,"end":30321617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233053.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32825106,"end":32825180,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000069122.18","gene_symbol":"ADGRF5","gene_name":"adhesion G protein-coupled receptor F5 [Source:HGNC Symbol;Acc:HGNC:19030]","synonyms":"KIAA0758,GPR116,DKFZp564O1923","biotype":"protein_coding","ncbi_id":"221395","summary":null,"start":46852512,"end":46954943,"strand":-1,"description":"adhesion G protein-coupled receptor F5 [Source:HGNC Symbol;Acc:HGNC:19030]"}, {"versioned_ensembl_gene_id":"ENSG00000103066.12","gene_symbol":"PLA2G15","gene_name":"phospholipase A2 group XV [Source:HGNC Symbol;Acc:HGNC:17163]","synonyms":"LYPLA3,LLPL,GXVPLA2","biotype":"protein_coding","ncbi_id":"23659","summary":"Lysophospholipases are enzymes that act on biological membranes to regulate the multifunctional lysophospholipids. The protein encoded by this gene hydrolyzes lysophosphatidylcholine to glycerophosphorylcholine and a free fatty acid. This enzyme is present in the plasma and thought to be associated with high-density lipoprotein. A later paper contradicts the function of this gene. It demonstrates that this gene encodes a lysosomal enzyme instead of a lysophospholipase and has both calcium-independent phospholipase A2 and transacylase activities. [provided by RefSeq, Jul 2008]","start":68245304,"end":68261062,"strand":1,"description":"phospholipase A2 group XV [Source:HGNC Symbol;Acc:HGNC:17163]"}, {"versioned_ensembl_gene_id":"ENSG00000260441.5","gene_symbol":"AC020978.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68256162,"end":68260443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268223.4","gene_symbol":"ARL14EPL","gene_name":"ADP ribosylation factor like GTPase 14 effector protein like [Source:HGNC Symbol;Acc:HGNC:44201]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644100","summary":null,"start":116032324,"end":116060118,"strand":1,"description":"ADP ribosylation factor like GTPase 14 effector protein like [Source:HGNC Symbol;Acc:HGNC:44201]"}, {"versioned_ensembl_gene_id":"ENSG00000277383.1","gene_symbol":"AC010331.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47607873,"end":47608454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278999.1","gene_symbol":"AC008985.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47661657,"end":47663895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186676.3","gene_symbol":"EEF1GP1","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44556]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646837","summary":null,"start":125033453,"end":125035301,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44556]"}, {"versioned_ensembl_gene_id":"ENSG00000167615.16","gene_symbol":"LENG8","gene_name":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]","synonyms":"pp13842,MGC40108,KIAA1932","biotype":"protein_coding","ncbi_id":"114823","summary":null,"start":54448887,"end":54462037,"strand":1,"description":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]"}, {"versioned_ensembl_gene_id":"ENSG00000117151.12","gene_symbol":"CTBS","gene_name":"chitobiase [Source:HGNC Symbol;Acc:HGNC:2496]","synonyms":"CTB","biotype":"protein_coding","ncbi_id":"1486","summary":"Chitobiase is a lysosomal glycosidase involved in degradation of asparagine-linked oligosaccharides on glycoproteins (Aronson and Kuranda, 1989 [PubMed 2531691]).[supplied by OMIM, Nov 2010]","start":84549606,"end":84574480,"strand":-1,"description":"chitobiase [Source:HGNC Symbol;Acc:HGNC:2496]"}, {"versioned_ensembl_gene_id":"ENSG00000256189.1","gene_symbol":"AP003717.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73991283,"end":73992180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257878.1","gene_symbol":"AC007298.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95996521,"end":96011489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205864.1","gene_symbol":"KRTAP5-6","gene_name":"keratin associated protein 5-6 [Source:HGNC Symbol;Acc:HGNC:23600]","synonyms":"KRTAP5.6","biotype":"protein_coding","ncbi_id":"440023","summary":null,"start":1697195,"end":1697755,"strand":1,"description":"keratin associated protein 5-6 [Source:HGNC Symbol;Acc:HGNC:23600]"}, {"versioned_ensembl_gene_id":"ENSG00000050030.13","gene_symbol":"NEXMIF","gene_name":"neurite extension and migration factor [Source:HGNC Symbol;Acc:HGNC:29433]","synonyms":"XPN,MRX98,KIDLIA,KIAA2022","biotype":"protein_coding","ncbi_id":"340533","summary":"An inversion on the X chromosome which disrupts this gene and a G-protein coupled purinergic receptor gene located in the pseudoautosomal region of the X chromosome has been linked to X linked cognitive disability.[provided by RefSeq, Mar 2009]","start":74732849,"end":74925485,"strand":-1,"description":"neurite extension and migration factor [Source:HGNC Symbol;Acc:HGNC:29433]"}, {"versioned_ensembl_gene_id":"ENSG00000258847.1","gene_symbol":"AL391261.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65957297,"end":66004523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267293.1","gene_symbol":"AC012569.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46028306,"end":46029829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110048.11","gene_symbol":"OSBP","gene_name":"oxysterol binding protein [Source:HGNC Symbol;Acc:HGNC:8503]","synonyms":"OSBP1","biotype":"protein_coding","ncbi_id":"5007","summary":"Oxysterol binding protein is an intracellular protein that is believed to transport sterols from lysosomes to the nucleus where the sterol down-regulates the genes for the LDL receptor, HMG-CoA reductase, and HMG synthetase [provided by RefSeq, Jul 2008]","start":59574398,"end":59616144,"strand":-1,"description":"oxysterol binding protein [Source:HGNC Symbol;Acc:HGNC:8503]"}, {"versioned_ensembl_gene_id":"ENSG00000251033.1","gene_symbol":"AC113347.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26711551,"end":26749997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188340.2","gene_symbol":"OR6N2","gene_name":"olfactory receptor family 6 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15035]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81442","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158774222,"end":158781204,"strand":-1,"description":"olfactory receptor family 6 subfamily N member 2 [Source:HGNC Symbol;Acc:HGNC:15035]"}, {"versioned_ensembl_gene_id":"ENSG00000248605.5","gene_symbol":"AC022140.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25404733,"end":25445925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279531.1","gene_symbol":"AC022140.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25425412,"end":25425599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204989.3","gene_symbol":"OR4D8P","gene_name":"olfactory receptor family 4 subfamily D member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15177]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59491652,"end":59492581,"strand":1,"description":"olfactory receptor family 4 subfamily D member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:15177]"}, {"versioned_ensembl_gene_id":"ENSG00000205678.7","gene_symbol":"TECRL","gene_name":"trans-2,3-enoyl-CoA reductase like [Source:HGNC Symbol;Acc:HGNC:27365]","synonyms":"TERL,SRD5A2L2,GPSN2L,DKFZp313D0829,DKFZp313B2333","biotype":"protein_coding","ncbi_id":"253017","summary":"The protein encoded by this gene contains a ubiquitin-like domain in the N-terminal region, three transmembrane segments and a C-terminal 3-oxo-5-alpha steroid 4-dehydrogenase domain. The protein belongs to the steroid 5-alpha reductase family. Mutations in this gene result in ventricular tachycardia, catecholaminergic polymorphic, 3. [provided by RefSeq, Apr 2017]","start":64275257,"end":64409468,"strand":-1,"description":"trans-2,3-enoyl-CoA reductase like [Source:HGNC Symbol;Acc:HGNC:27365]"}, {"versioned_ensembl_gene_id":"ENSG00000168487.17","gene_symbol":"BMP1","gene_name":"bone morphogenetic protein 1 [Source:HGNC Symbol;Acc:HGNC:1067]","synonyms":"PCOLC","biotype":"protein_coding","ncbi_id":"649","summary":"This gene encodes a protein that is capable of inducing formation of cartilage in vivo. Although other bone morphogenetic proteins are members of the TGF-beta superfamily, this gene encodes a protein that is not closely related to other known growth factors. This gene is expressed as alternatively spliced variants that share an N-terminal protease domain but differ in their C-terminal region. [provided by RefSeq, Aug 2008]","start":22164736,"end":22212326,"strand":1,"description":"bone morphogenetic protein 1 [Source:HGNC Symbol;Acc:HGNC:1067]"}, {"versioned_ensembl_gene_id":"ENSG00000230160.1","gene_symbol":"AC004854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44919669,"end":44920329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232314.1","gene_symbol":"PSMC1P13","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39788]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422305","summary":null,"start":69894101,"end":69895085,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39788]"}, {"versioned_ensembl_gene_id":"ENSG00000223823.1","gene_symbol":"LINC01342","gene_name":"long intergenic non-protein coding RNA 1342 [Source:HGNC Symbol;Acc:HGNC:50551]","synonyms":null,"biotype":"lincRNA","ncbi_id":"254099","summary":null,"start":1137017,"end":1144056,"strand":1,"description":"long intergenic non-protein coding RNA 1342 [Source:HGNC Symbol;Acc:HGNC:50551]"}, {"versioned_ensembl_gene_id":"ENSG00000234816.2","gene_symbol":"HIST1H2APS5","gene_name":"histone cluster 1 H2A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4728]","synonyms":"pH2A/f,H2AFFP","biotype":"unprocessed_pseudogene","ncbi_id":"10341","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This histone pseudogene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Oct 2015]","start":26043989,"end":26044357,"strand":1,"description":"histone cluster 1 H2A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4728]"}, {"versioned_ensembl_gene_id":"ENSG00000203585.3","gene_symbol":"LINC02408","gene_name":"long intergenic non-protein coding RNA 2408 [Source:HGNC Symbol;Acc:HGNC:53337]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507175","summary":null,"start":67519829,"end":67567126,"strand":1,"description":"long intergenic non-protein coding RNA 2408 [Source:HGNC Symbol;Acc:HGNC:53337]"}, {"versioned_ensembl_gene_id":"ENSG00000182208.13","gene_symbol":"MOB2","gene_name":"MOB kinase activator 2 [Source:HGNC Symbol;Acc:HGNC:24904]","synonyms":"HCCA2","biotype":"protein_coding","ncbi_id":"81532","summary":null,"start":1469457,"end":1501247,"strand":-1,"description":"MOB kinase activator 2 [Source:HGNC Symbol;Acc:HGNC:24904]"}, {"versioned_ensembl_gene_id":"ENSG00000259967.1","gene_symbol":"AC087761.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80165923,"end":80166980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177943.13","gene_symbol":"MAMDC4","gene_name":"MAM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24083]","synonyms":"AEGP,DKFZp434M1411","biotype":"protein_coding","ncbi_id":"158056","summary":null,"start":136850943,"end":136860799,"strand":1,"description":"MAM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24083]"}, {"versioned_ensembl_gene_id":"ENSG00000232434.2","gene_symbol":"C9orf172","gene_name":"chromosome 9 open reading frame 172 [Source:HGNC Symbol;Acc:HGNC:37284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"389813","summary":null,"start":136844415,"end":136848801,"strand":1,"description":"chromosome 9 open reading frame 172 [Source:HGNC Symbol;Acc:HGNC:37284]"}, {"versioned_ensembl_gene_id":"ENSG00000277548.1","gene_symbol":"AC018926.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55346347,"end":55346752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237955.1","gene_symbol":"AC245884.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54379489,"end":54379960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275897.1","gene_symbol":"AC021491.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50475819,"end":50478391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226971.1","gene_symbol":"AL606490.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48446893,"end":48448879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253653.1","gene_symbol":"AC009185.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157260122,"end":157266625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266378.1","gene_symbol":"AC005224.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14327335,"end":14329474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266709.1","gene_symbol":"AC005224.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14303854,"end":14305505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216723.1","gene_symbol":"NUDT19P3","gene_name":"nudix hydrolase 19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43587]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422450","summary":null,"start":114019621,"end":114020483,"strand":-1,"description":"nudix hydrolase 19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43587]"}, {"versioned_ensembl_gene_id":"ENSG00000283257.1","gene_symbol":"AP001184.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67538899,"end":67540584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254799.1","gene_symbol":"SLC25A47P1","gene_name":"solute carrier family 25 member 47 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43860]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105369316","summary":null,"start":59263389,"end":59263802,"strand":-1,"description":"solute carrier family 25 member 47 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43860]"}, {"versioned_ensembl_gene_id":"ENSG00000146425.10","gene_symbol":"DYNLT1","gene_name":"dynein light chain Tctex-type 1 [Source:HGNC Symbol;Acc:HGNC:11697]","synonyms":"TCTEL1","biotype":"protein_coding","ncbi_id":"6993","summary":"This gene encodes a component of the motor complex, cytoplasmic dynein, which transports cellular cargo along microtubules in the cell. The encoded protein regulates the length of primary cilia which are sensory organelles found on the surface of cells. The protein encoded by this gene interacts with viral proteins, like the minor capsid protein L2 of human papillomavirus, and is required for dynein-mediated delivery of the viral nucleic acid to the host nucleus. This protein interacts with oncogenic nucleoporins to disrupt gene regulation and cause leukemic transformation. Pseudogenes of this gene are present on chromosomes 4 and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014]","start":158636474,"end":158644739,"strand":-1,"description":"dynein light chain Tctex-type 1 [Source:HGNC Symbol;Acc:HGNC:11697]"}, {"versioned_ensembl_gene_id":"ENSG00000234929.1","gene_symbol":"AC018685.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2641989,"end":2656630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270458.1","gene_symbol":"AC009779.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55662337,"end":55662501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136875.12","gene_symbol":"PRPF4","gene_name":"pre-mRNA processing factor 4 [Source:HGNC Symbol;Acc:HGNC:17349]","synonyms":"SNRNP60,Prp4p,PRP4,HPRP4P,HPRP4","biotype":"protein_coding","ncbi_id":"9128","summary":"The protein encoded by this gene is part of a heteromeric complex that binds U4, U5, and U6 small nuclear RNAs and is involved in pre-mRNA splicing. The encoded protein also is a mitotic checkpoint protein and a regulator of chemoresistance in human ovarian cancer. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2016]","start":113275343,"end":113292905,"strand":1,"description":"pre-mRNA processing factor 4 [Source:HGNC Symbol;Acc:HGNC:17349]"}, {"versioned_ensembl_gene_id":"ENSG00000275185.1","gene_symbol":"AC130324.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30899110,"end":30899651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230113.1","gene_symbol":"AC138207.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30956280,"end":30956961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227672.1","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31273691,"end":31274890,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000196591.11","gene_symbol":"HDAC2","gene_name":"histone deacetylase 2 [Source:HGNC Symbol;Acc:HGNC:4853]","synonyms":"YAF1,RPD3","biotype":"protein_coding","ncbi_id":"3066","summary":"This gene product belongs to the histone deacetylase family. Histone deacetylases act via the formation of large multiprotein complexes, and are responsible for the deacetylation of lysine residues at the N-terminal regions of core histones (H2A, H2B, H3 and H4). This protein forms transcriptional repressor complexes by associating with many different proteins, including YY1, a mammalian zinc-finger transcription factor. Thus, it plays an important role in transcriptional regulation, cell cycle progression and developmental events. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":113933028,"end":114011308,"strand":-1,"description":"histone deacetylase 2 [Source:HGNC Symbol;Acc:HGNC:4853]"}, {"versioned_ensembl_gene_id":"ENSG00000146701.11","gene_symbol":"MDH2","gene_name":"malate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:6971]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4191","summary":"Malate dehydrogenase catalyzes the reversible oxidation of malate to oxaloacetate, utilizing the NAD/NADH cofactor system in the citric acid cycle. The protein encoded by this gene is localized to the mitochondria and may play pivotal roles in the malate-aspartate shuttle that operates in the metabolic coordination between cytosol and mitochondria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":76048051,"end":76067508,"strand":1,"description":"malate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:6971]"}, {"versioned_ensembl_gene_id":"ENSG00000204677.10","gene_symbol":"FAM153C","gene_name":"family with sequence similarity 153 member C [Source:HGNC Symbol;Acc:HGNC:33936]","synonyms":"NY-REN-7-like","biotype":"protein_coding","ncbi_id":"653316","summary":null,"start":178006405,"end":178055559,"strand":1,"description":"family with sequence similarity 153 member C [Source:HGNC Symbol;Acc:HGNC:33936]"}, {"versioned_ensembl_gene_id":"ENSG00000276763.1","gene_symbol":"AC069499.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108574683,"end":108575064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225501.1","gene_symbol":"SNRPFP3","gene_name":"small nuclear ribonucleoprotein polypeptide F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39666]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874422","summary":null,"start":69101832,"end":69102056,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39666]"}, {"versioned_ensembl_gene_id":"ENSG00000280580.1","gene_symbol":"LINC02342","gene_name":"long intergenic non-protein coding RNA 2342 [Source:HGNC Symbol;Acc:HGNC:53262]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370253","summary":null,"start":68878380,"end":68893573,"strand":1,"description":"long intergenic non-protein coding RNA 2342 [Source:HGNC Symbol;Acc:HGNC:53262]"}, {"versioned_ensembl_gene_id":"ENSG00000272870.1","gene_symbol":"AC097534.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173363780,"end":173370446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247121.6","gene_symbol":"AC009126.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96814028,"end":96935809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113732.8","gene_symbol":"ATP6V0E1","gene_name":"ATPase H+ transporting V0 subunit e1 [Source:HGNC Symbol;Acc:HGNC:863]","synonyms":"M9.2,ATP6V0E,ATP6H","biotype":"protein_coding","ncbi_id":"8992","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is possibly part of the V0 subunit. Since two nontranscribed pseudogenes have been found in dog, it is possible that the localization to chromosome 2 for this gene by radiation hybrid mapping is representing a pseudogene. Genomic mapping puts the chromosomal location on 5q35.3. [provided by RefSeq, Jul 2008]","start":172983757,"end":173035445,"strand":1,"description":"ATPase H+ transporting V0 subunit e1 [Source:HGNC Symbol;Acc:HGNC:863]"}, {"versioned_ensembl_gene_id":"ENSG00000254328.1","gene_symbol":"AC008429.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172986680,"end":172987198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179626.4","gene_symbol":"OR6C4","gene_name":"olfactory receptor family 6 subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:19632]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341418","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55549602,"end":55555832,"strand":1,"description":"olfactory receptor family 6 subfamily C member 4 [Source:HGNC Symbol;Acc:HGNC:19632]"}, {"versioned_ensembl_gene_id":"ENSG00000225029.3","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"D84394.7,USP8P,KIAA0055-hom","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31268956,"end":31272128,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000100344.10","gene_symbol":"PNPLA3","gene_name":"patatin like phospholipase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18590]","synonyms":"iPLA2epsilon,FLJ22012,dJ796I17.1,C22orf20,ADPN,adiponutrin","biotype":"protein_coding","ncbi_id":"80339","summary":"The protein encoded by this gene is a triacylglycerol lipase that mediates triacylglycerol hydrolysis in adipocytes. The encoded protein, which appears to be membrane bound, may be involved in the balance of energy usage/storage in adipocytes. [provided by RefSeq, Jul 2008]","start":43923739,"end":43964488,"strand":1,"description":"patatin like phospholipase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:18590]"}, {"versioned_ensembl_gene_id":"ENSG00000110583.12","gene_symbol":"NAA40","gene_name":"N(alpha)-acetyltransferase 40, NatD catalytic subunit [Source:HGNC Symbol;Acc:HGNC:25845]","synonyms":"NAT11,FLJ13848","biotype":"protein_coding","ncbi_id":"79829","summary":null,"start":63938959,"end":63957328,"strand":1,"description":"N(alpha)-acetyltransferase 40, NatD catalytic subunit [Source:HGNC Symbol;Acc:HGNC:25845]"}, {"versioned_ensembl_gene_id":"ENSG00000130714.15","gene_symbol":"POMT1","gene_name":"protein O-mannosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:9202]","synonyms":"LGMD2K","biotype":"protein_coding","ncbi_id":"10585","summary":"The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2008]","start":131502902,"end":131523806,"strand":1,"description":"protein O-mannosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:9202]"}, {"versioned_ensembl_gene_id":"ENSG00000265494.1","gene_symbol":"AC005304.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13909231,"end":13911212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176102.11","gene_symbol":"CSTF3","gene_name":"cleavage stimulation factor subunit 3 [Source:HGNC Symbol;Acc:HGNC:2485]","synonyms":"CstF-77","biotype":"protein_coding","ncbi_id":"1479","summary":"The protein encoded by this gene is one of three (including CSTF1 and CSTF2) cleavage stimulation factors that combine to form the cleavage stimulation factor complex (CSTF). This complex is involved in the polyadenylation and 3' end cleavage of pre-mRNAs. The encoded protein functions as a homodimer and interacts directly with both CSTF1 and CSTF2 in the CSTF complex. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33077188,"end":33162371,"strand":-1,"description":"cleavage stimulation factor subunit 3 [Source:HGNC Symbol;Acc:HGNC:2485]"}, {"versioned_ensembl_gene_id":"ENSG00000172062.16","gene_symbol":"SMN1","gene_name":"survival of motor neuron 1, telomeric [Source:HGNC Symbol;Acc:HGNC:11117]","synonyms":"SMA2,SMA1,TDRD16A,SMA,SMNT,GEMIN1,SMA@,BCD541,SMA3","biotype":"protein_coding","ncbi_id":"6606","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. However, mutations in this gene, the telomeric copy, are associated with spinal muscular atrophy; mutations in the centromeric copy do not lead to disease. The centromeric copy may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Multiple transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2014]","start":70925030,"end":70953942,"strand":1,"description":"survival of motor neuron 1, telomeric [Source:HGNC Symbol;Acc:HGNC:11117]"}, {"versioned_ensembl_gene_id":"ENSG00000227502.2","gene_symbol":"LINC01268","gene_name":"long intergenic non-protein coding RNA 1268 [Source:HGNC Symbol;Acc:HGNC:50323]","synonyms":"LOC285758","biotype":"lincRNA","ncbi_id":"285758","summary":null,"start":113868013,"end":113873351,"strand":-1,"description":"long intergenic non-protein coding RNA 1268 [Source:HGNC Symbol;Acc:HGNC:50323]"}, {"versioned_ensembl_gene_id":"ENSG00000180910.7","gene_symbol":"TTTY11","gene_name":"testis-specific transcript, Y-linked 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18492]","synonyms":"TTY11,NCRNA00134","biotype":"lincRNA","ncbi_id":"83866","summary":null,"start":8783310,"end":8817382,"strand":-1,"description":"testis-specific transcript, Y-linked 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18492]"}, {"versioned_ensembl_gene_id":"ENSG00000182053.12","gene_symbol":"TRIM49B","gene_name":"tripartite motif containing 49B [Source:HGNC Symbol;Acc:HGNC:42955]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283116","summary":null,"start":49027501,"end":49038451,"strand":1,"description":"tripartite motif containing 49B [Source:HGNC Symbol;Acc:HGNC:42955]"}, {"versioned_ensembl_gene_id":"ENSG00000277453.1","gene_symbol":"AC010271.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40426115,"end":40426702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109475.16","gene_symbol":"RPL34","gene_name":"ribosomal protein L34 [Source:HGNC Symbol;Acc:HGNC:10340]","synonyms":"L34","biotype":"protein_coding","ncbi_id":"6164","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L34E family of ribosomal proteins. It is located in the cytoplasm. This gene originally was thought to be located at 17q21, but it has been mapped to 4q. Overexpression of this gene has been observed in some cancer cells. Alternative splicing results in multiple transcript variants, all encoding the same isoform. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Feb 2016]","start":108620566,"end":108630412,"strand":1,"description":"ribosomal protein L34 [Source:HGNC Symbol;Acc:HGNC:10340]"}, {"versioned_ensembl_gene_id":"ENSG00000271304.1","gene_symbol":"AL133507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35989515,"end":35990436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275807.1","gene_symbol":"AC145285.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28822431,"end":28823969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165792.17","gene_symbol":"METTL17","gene_name":"methyltransferase like 17 [Source:HGNC Symbol;Acc:HGNC:19280]","synonyms":"METT11D1,FLJ20859","biotype":"protein_coding","ncbi_id":"64745","summary":null,"start":20989770,"end":20997035,"strand":1,"description":"methyltransferase like 17 [Source:HGNC Symbol;Acc:HGNC:19280]"}, {"versioned_ensembl_gene_id":"ENSG00000224553.1","gene_symbol":"AC008065.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171374931,"end":171375278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241769.7","gene_symbol":"LINC00893","gene_name":"long intergenic non-protein coding RNA 893 [Source:HGNC Symbol;Acc:HGNC:44265]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131434","summary":null,"start":149527591,"end":149540959,"strand":-1,"description":"long intergenic non-protein coding RNA 893 [Source:HGNC Symbol;Acc:HGNC:44265]"}, {"versioned_ensembl_gene_id":"ENSG00000226727.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29887395,"end":29888526,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000132313.14","gene_symbol":"MRPL35","gene_name":"mitochondrial ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:14489]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51318","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Sequence analysis identified three transcript variants. Pseudogenes corresponding to this gene are found on chromosomes 6p, 10q, and Xp. [provided by RefSeq, Jul 2008]","start":86199355,"end":86213794,"strand":1,"description":"mitochondrial ribosomal protein L35 [Source:HGNC Symbol;Acc:HGNC:14489]"}, {"versioned_ensembl_gene_id":"ENSG00000223574.1","gene_symbol":"TPMTP4","gene_name":"thiopurine S-methyltransferase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44567]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129298","summary":null,"start":86128893,"end":86129570,"strand":-1,"description":"thiopurine S-methyltransferase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44567]"}, {"versioned_ensembl_gene_id":"ENSG00000108406.9","gene_symbol":"DHX40","gene_name":"DEAH-box helicase 40 [Source:HGNC Symbol;Acc:HGNC:18018]","synonyms":"PAD,FLJ22060,DDX40,ARG147","biotype":"protein_coding","ncbi_id":"79665","summary":"This gene encodes a member of the DExH/D box family of ATP-dependent RNA helicases that have an essential role in RNA metabolism. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 17.[provided by RefSeq, Oct 2009]","start":59565525,"end":59608345,"strand":1,"description":"DEAH-box helicase 40 [Source:HGNC Symbol;Acc:HGNC:18018]"}, {"versioned_ensembl_gene_id":"ENSG00000281664.1","gene_symbol":"LINC00538","gene_name":"long intergenic non-protein coding RNA 538 [Source:HGNC Symbol;Acc:HGNC:43655]","synonyms":"Yiya,PROX1UT","biotype":"lincRNA","ncbi_id":"100861504","summary":null,"start":213924749,"end":213926654,"strand":-1,"description":"long intergenic non-protein coding RNA 538 [Source:HGNC Symbol;Acc:HGNC:43655]"}, {"versioned_ensembl_gene_id":"ENSG00000281688.2","gene_symbol":"NF1P9","gene_name":"neurofibromin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51736]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101930150","summary":null,"start":21490371,"end":21509391,"strand":-1,"description":"neurofibromin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51736]"}, {"versioned_ensembl_gene_id":"ENSG00000206337.10","gene_symbol":"HCP5","gene_name":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]","synonyms":"D6S2650E,P5-1","biotype":"sense_overlapping","ncbi_id":"10866","summary":null,"start":31400702,"end":31477506,"strand":1,"description":"HLA complex P5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21659]"}, {"versioned_ensembl_gene_id":"ENSG00000106133.17","gene_symbol":"NSUN5P2","gene_name":"NOP2/Sun RNA methyltransferase family member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16609]","synonyms":"MGC15057,NOL1R2,FLJ11626,DKFZp434K058,WBSCR20C,WBSCR20B,NSUN5C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"260294","summary":"This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [provided by RefSeq, Jul 2013]","start":72947581,"end":72954790,"strand":-1,"description":"NOP2/Sun RNA methyltransferase family member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16609]"}, {"versioned_ensembl_gene_id":"ENSG00000267287.1","gene_symbol":"AC068473.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":79576460,"end":79589010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125731.12","gene_symbol":"SH2D3A","gene_name":"SH2 domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16885]","synonyms":"NSP1","biotype":"protein_coding","ncbi_id":"10045","summary":null,"start":6752160,"end":6767588,"strand":-1,"description":"SH2 domain containing 3A [Source:HGNC Symbol;Acc:HGNC:16885]"}, {"versioned_ensembl_gene_id":"ENSG00000121413.12","gene_symbol":"ZSCAN18","gene_name":"zinc finger and SCAN domain containing 18 [Source:HGNC Symbol;Acc:HGNC:21037]","synonyms":"ZNF447,FLJ12895","biotype":"protein_coding","ncbi_id":"65982","summary":null,"start":58083838,"end":58118427,"strand":-1,"description":"zinc finger and SCAN domain containing 18 [Source:HGNC Symbol;Acc:HGNC:21037]"}, {"versioned_ensembl_gene_id":"ENSG00000175073.7","gene_symbol":"VCPIP1","gene_name":"valosin containing protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30897]","synonyms":"VCIP135,KIAA1850,FLJ23132,DUBA3","biotype":"protein_coding","ncbi_id":"80124","summary":null,"start":66628487,"end":66667217,"strand":-1,"description":"valosin containing protein interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:30897]"}, {"versioned_ensembl_gene_id":"ENSG00000248346.1","gene_symbol":"AC092435.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146957438,"end":146975457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186440.2","gene_symbol":"OR6P1","gene_name":"olfactory receptor family 6 subfamily P member 1 [Source:HGNC Symbol;Acc:HGNC:15036]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128366","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158560606,"end":158570580,"strand":-1,"description":"olfactory receptor family 6 subfamily P member 1 [Source:HGNC Symbol;Acc:HGNC:15036]"}, {"versioned_ensembl_gene_id":"ENSG00000171643.13","gene_symbol":"S100Z","gene_name":"S100 calcium binding protein Z [Source:HGNC Symbol;Acc:HGNC:30367]","synonyms":"Gm625,S100-zeta","biotype":"protein_coding","ncbi_id":"170591","summary":"Members of the S100 protein family contain 2 calcium-binding EF-hands and exhibit cell-type specific expression patterns. For additional background information on S100 proteins, see MIM 114085.[supplied by OMIM, Mar 2008]","start":76850001,"end":76921650,"strand":1,"description":"S100 calcium binding protein Z [Source:HGNC Symbol;Acc:HGNC:30367]"}, {"versioned_ensembl_gene_id":"ENSG00000214309.4","gene_symbol":"MBLAC1","gene_name":"metallo-beta-lactamase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22180]","synonyms":"MGC49416","biotype":"protein_coding","ncbi_id":"255374","summary":null,"start":100126694,"end":100128498,"strand":1,"description":"metallo-beta-lactamase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22180]"}, {"versioned_ensembl_gene_id":"ENSG00000237164.1","gene_symbol":"SLC25A15P2","gene_name":"solute carrier family 25 member 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39843]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874522","summary":null,"start":19411231,"end":19416188,"strand":1,"description":"solute carrier family 25 member 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39843]"}, {"versioned_ensembl_gene_id":"ENSG00000235974.1","gene_symbol":"VN2R19P","gene_name":"vomeronasal 2 receptor 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:33225]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100033407","summary":null,"start":58012589,"end":58025926,"strand":-1,"description":"vomeronasal 2 receptor 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:33225]"}, {"versioned_ensembl_gene_id":"ENSG00000102452.15","gene_symbol":"NALCN","gene_name":"sodium leak channel, non-selective [Source:HGNC Symbol;Acc:HGNC:19082]","synonyms":"VGCNL1,CanIon,bA430M15.1","biotype":"protein_coding","ncbi_id":"259232","summary":"This gene encodes a voltage-independent, nonselective cation channel which belongs to a family of voltage-gated sodium and calcium channels that regulates the resting membrane potential and excitability of neurons. This family is expressed throughout the nervous system and conducts a persistent sodium leak current that contributes to tonic neuronal excitability. The encoded protein forms a channelosome complex that includes G-protein-coupled receptors, UNC-79, UNC-80, NCA localization factor-1, and src family tyrosine kinases. Naturally occurring mutations in this gene are associated with infantile neuroaxonal dystrophy, infantile hypotonia with psychomotor retardation and characteristic facies (IHPRF) syndrome, and congenital contractures of the limbs and face with hypotonia and developmental delay (CLIFAHDD) syndrome. A knockout of the orthologous gene in mice results in paralysis with a severely disrupted respiratory rhythm, and lethality within 24 hours after birth. [provided by RefSeq, Apr 2017]","start":101053776,"end":101416492,"strand":-1,"description":"sodium leak channel, non-selective [Source:HGNC Symbol;Acc:HGNC:19082]"}, {"versioned_ensembl_gene_id":"ENSG00000250694.1","gene_symbol":"AC010387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24352309,"end":24353443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223707.2","gene_symbol":"SFR1P2","gene_name":"SFR1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51532]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730792","summary":null,"start":85849410,"end":85850139,"strand":-1,"description":"SFR1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51532]"}, {"versioned_ensembl_gene_id":"ENSG00000230107.1","gene_symbol":"AL022316.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42438023,"end":42446195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242798.1","gene_symbol":"AC073842.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100115214,"end":100127139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261714.2","gene_symbol":"AC105137.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75415249,"end":75416020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275645.1","gene_symbol":"AC068338.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75346744,"end":75347161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113441.15","gene_symbol":"LNPEP","gene_name":"leucyl and cystinyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:6656]","synonyms":"PLAP,P-LAP,IRAP,CAP","biotype":"protein_coding","ncbi_id":"4012","summary":"This gene encodes a zinc-dependent aminopeptidase that cleaves vasopressin, oxytocin, lys-bradykinin, met-enkephalin, dynorphin A and other peptide hormones. The protein can be secreted in maternal serum, reside in intracellular vesicles with the insulin-responsive glucose transporter GLUT4, or form a type II integral membrane glycoprotein. The protein catalyzes the final step in the conversion of angiotensinogen to angiotensin IV (AT4) and is also a receptor for AT4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":96935394,"end":97037515,"strand":1,"description":"leucyl and cystinyl aminopeptidase [Source:HGNC Symbol;Acc:HGNC:6656]"}, {"versioned_ensembl_gene_id":"ENSG00000129355.6","gene_symbol":"CDKN2D","gene_name":"cyclin dependent kinase inhibitor 2D [Source:HGNC Symbol;Acc:HGNC:1790]","synonyms":"p19,INK4D","biotype":"protein_coding","ncbi_id":"1032","summary":"The protein encoded by this gene is a member of the INK4 family of cyclin-dependent kinase inhibitors. This protein has been shown to form a stable complex with CDK4 or CDK6, and prevent the activation of the CDK kinases, thus function as a cell growth regulator that controls cell cycle G1 progression. The abundance of the transcript of this gene was found to oscillate in a cell-cycle dependent manner with the lowest expression at mid G1 and a maximal expression during S phase. The negative regulation of the cell cycle involved in this protein was shown to participate in repressing neuronal proliferation, as well as spermatogenesis. Two alternatively spliced variants of this gene, which encode an identical protein, have been reported. [provided by RefSeq, Jul 2008]","start":10566462,"end":10569059,"strand":-1,"description":"cyclin dependent kinase inhibitor 2D [Source:HGNC Symbol;Acc:HGNC:1790]"}, {"versioned_ensembl_gene_id":"ENSG00000273956.1","gene_symbol":"AC005632.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21526824,"end":21531141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215349.2","gene_symbol":"MRPL3P1","gene_name":"mitochondrial ribosomal protein L3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29701]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359739","summary":null,"start":19304593,"end":19305625,"strand":-1,"description":"mitochondrial ribosomal protein L3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29701]"}, {"versioned_ensembl_gene_id":"ENSG00000203758.4","gene_symbol":"OR10T1P","gene_name":"olfactory receptor family 10 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14812]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79514","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158445068,"end":158446014,"strand":-1,"description":"olfactory receptor family 10 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14812]"}, {"versioned_ensembl_gene_id":"ENSG00000225648.5","gene_symbol":"SBDSP1","gene_name":"SBDS, ribosome maturation factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21646]","synonyms":"SBDSP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"155370","summary":null,"start":72829425,"end":72836701,"strand":1,"description":"SBDS, ribosome maturation factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21646]"}, {"versioned_ensembl_gene_id":"ENSG00000262165.2","gene_symbol":"AC233723.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4801159,"end":4807013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255551.1","gene_symbol":"AC027369.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48880111,"end":48885237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254920.1","gene_symbol":"AC027369.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48893256,"end":48898703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232460.4","gene_symbol":"BMPR1APS2","gene_name":"bone morphogenetic protein receptor type 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533800","summary":null,"start":121361854,"end":121362865,"strand":-1,"description":"bone morphogenetic protein receptor type 1A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21743]"}, {"versioned_ensembl_gene_id":"ENSG00000106290.14","gene_symbol":"TAF6","gene_name":"TATA-box binding protein associated factor 6 [Source:HGNC Symbol;Acc:HGNC:11540]","synonyms":"TAFII85,TAFII80,TAFII70,TAF2E,MGC:8964","biotype":"protein_coding","ncbi_id":"6878","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the smaller subunits of TFIID that binds weakly to TBP but strongly to TAF1, the largest subunit of TFIID. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":100107070,"end":100119841,"strand":-1,"description":"TATA-box binding protein associated factor 6 [Source:HGNC Symbol;Acc:HGNC:11540]"}, {"versioned_ensembl_gene_id":"ENSG00000250332.1","gene_symbol":"AC010460.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23303565,"end":23305143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239463.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32982065,"end":33004180,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000231681.2","gene_symbol":"AC020743.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50202001,"end":50262994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243236.6","gene_symbol":"GSTA9P","gene_name":"glutathione S-transferase alpha 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:49902]","synonyms":"GSTAP4,GSTA4P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100174857","summary":null,"start":52939726,"end":52957521,"strand":-1,"description":"glutathione S-transferase alpha 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:49902]"}, {"versioned_ensembl_gene_id":"ENSG00000249404.1","gene_symbol":"AC010445.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23013048,"end":23014527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241018.1","gene_symbol":"RCC2P5","gene_name":"regulator of chromosome condensation 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42381]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131442","summary":null,"start":96753185,"end":96754671,"strand":1,"description":"regulator of chromosome condensation 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42381]"}, {"versioned_ensembl_gene_id":"ENSG00000239344.1","gene_symbol":"AC090686.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103768281,"end":103769029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234000.8","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30666650,"end":30678156,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000255671.1","gene_symbol":"AC007406.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":193036,"end":194130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256577.2","gene_symbol":"AC007406.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":203642,"end":205094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267609.2","gene_symbol":"SNX33P1","gene_name":"sorting nexin 33 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48590]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533624","summary":null,"start":16034776,"end":16036537,"strand":-1,"description":"sorting nexin 33 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48590]"}, {"versioned_ensembl_gene_id":"ENSG00000283638.2","gene_symbol":"AC002407.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":134168911,"end":134174089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263266.2","gene_symbol":"RPS7P1","gene_name":"ribosomal protein S7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388363","summary":null,"start":28467822,"end":28468406,"strand":1,"description":"ribosomal protein S7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17081]"}, {"versioned_ensembl_gene_id":"ENSG00000177551.5","gene_symbol":"NHLH2","gene_name":"nescient helix-loop-helix 2 [Source:HGNC Symbol;Acc:HGNC:7818]","synonyms":"NSCL2,HEN2,bHLHa34","biotype":"protein_coding","ncbi_id":"4808","summary":null,"start":115836377,"end":115843917,"strand":-1,"description":"nescient helix-loop-helix 2 [Source:HGNC Symbol;Acc:HGNC:7818]"}, {"versioned_ensembl_gene_id":"ENSG00000240791.1","gene_symbol":"MTND4LP7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42241]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075236","summary":null,"start":92110575,"end":92110868,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42241]"}, {"versioned_ensembl_gene_id":"ENSG00000215263.2","gene_symbol":"AC025750.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42532766,"end":42533442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147180.16","gene_symbol":"ZNF711","gene_name":"zinc finger protein 711 [Source:HGNC Symbol;Acc:HGNC:13128]","synonyms":"ZNF6,ZNF5,ZNF4,Zfp711,MRX97,dJ75N13.1,CMPX1","biotype":"protein_coding","ncbi_id":"7552","summary":"This gene encodes a zinc finger protein of unknown function. It bears similarity to a zinc finger protein which acts as a transcriptional activator. This gene lies in a region of the X chromosome which has been associated with cognitive disability. [provided by RefSeq, Jul 2008]","start":85244032,"end":85273362,"strand":1,"description":"zinc finger protein 711 [Source:HGNC Symbol;Acc:HGNC:13128]"}, {"versioned_ensembl_gene_id":"ENSG00000184517.11","gene_symbol":"ZFP1","gene_name":"ZFP1 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23328]","synonyms":"ZNF475,FLJ34243","biotype":"protein_coding","ncbi_id":"162239","summary":"This gene belongs to the zinc finger protein family. Some members of this family bind to DNA by zinc-mediated secondary structures called zinc fingers, and are involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":75148492,"end":75172236,"strand":1,"description":"ZFP1 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23328]"}, {"versioned_ensembl_gene_id":"ENSG00000100815.12","gene_symbol":"TRIP11","gene_name":"thyroid hormone receptor interactor 11 [Source:HGNC Symbol;Acc:HGNC:12305]","synonyms":"Trip230,GMAP210,GMAP-210,CEV14","biotype":"protein_coding","ncbi_id":"9321","summary":"This gene was identified based on the interaction of its protein product with thyroid hormone receptor beta. This protein is associated with the Golgi apparatus. The N-terminal region of the protein binds Golgi membranes and the C-terminal region binds the minus ends of microtubules; thus, the protein is thought to play a role in assembly and maintenance of the Golgi ribbon structure around the centrosome. Mutations in this gene cause achondrogenesis type IA.[provided by RefSeq, Mar 2010]","start":91965991,"end":92040896,"strand":-1,"description":"thyroid hormone receptor interactor 11 [Source:HGNC Symbol;Acc:HGNC:12305]"}, {"versioned_ensembl_gene_id":"ENSG00000137574.10","gene_symbol":"TGS1","gene_name":"trimethylguanosine synthase 1 [Source:HGNC Symbol;Acc:HGNC:17843]","synonyms":"PIMT,NCOA6IP","biotype":"protein_coding","ncbi_id":"96764","summary":null,"start":55773142,"end":55825448,"strand":1,"description":"trimethylguanosine synthase 1 [Source:HGNC Symbol;Acc:HGNC:17843]"}, {"versioned_ensembl_gene_id":"ENSG00000248685.5","gene_symbol":"LINC02484","gene_name":"long intergenic non-protein coding RNA 2484 [Source:HGNC Symbol;Acc:HGNC:53459]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374394","summary":null,"start":34120894,"end":34269747,"strand":-1,"description":"long intergenic non-protein coding RNA 2484 [Source:HGNC Symbol;Acc:HGNC:53459]"}, {"versioned_ensembl_gene_id":"ENSG00000254786.1","gene_symbol":"AP001636.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58995439,"end":58999689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257870.1","gene_symbol":"AC027287.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55009746,"end":55014247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134909.18","gene_symbol":"ARHGAP32","gene_name":"Rho GTPase activating protein 32 [Source:HGNC Symbol;Acc:HGNC:17399]","synonyms":"RICS,MGC1892,KIAA0712,GRIT,GC-GAP","biotype":"protein_coding","ncbi_id":"9743","summary":"RICS is a neuron-associated GTPase-activating protein that may regulate dendritic spine morphology and strength by modulating Rho GTPase (see RHOA; MIM 165390) activity (Okabe et al., 2003 [PubMed 12531901]).[supplied by OMIM, Mar 2008]","start":128965060,"end":129279324,"strand":-1,"description":"Rho GTPase activating protein 32 [Source:HGNC Symbol;Acc:HGNC:17399]"}, {"versioned_ensembl_gene_id":"ENSG00000267401.1","gene_symbol":"AC090621.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60294151,"end":60301118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114354.13","gene_symbol":"TFG","gene_name":"TRK-fused gene [Source:HGNC Symbol;Acc:HGNC:11758]","synonyms":"TF6,SPG57,FLJ36137","biotype":"protein_coding","ncbi_id":"10342","summary":"There are several documented fusion oncoproteins encoded partially by this gene. This gene also participates in several oncogenic rearrangements resulting in anaplastic lymphoma and mixoid chondrosarcoma, and may play a role in the NF-kappaB pathway. Multiple transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]","start":100709331,"end":100748966,"strand":1,"description":"TRK-fused gene [Source:HGNC Symbol;Acc:HGNC:11758]"}, {"versioned_ensembl_gene_id":"ENSG00000266561.2","gene_symbol":"AC011195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58675286,"end":58675462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249452.2","gene_symbol":"AC093878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33238239,"end":33238670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236284.1","gene_symbol":"VN1R31P","gene_name":"vomeronasal 1 receptor 31 pseudogene [Source:HGNC Symbol;Acc:HGNC:37351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312787","summary":null,"start":63367427,"end":63368156,"strand":-1,"description":"vomeronasal 1 receptor 31 pseudogene [Source:HGNC Symbol;Acc:HGNC:37351]"}, {"versioned_ensembl_gene_id":"ENSG00000226450.2","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42149886,"end":42155001,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000235957.1","gene_symbol":"COX7CP1","gene_name":"cytochrome c oxidase subunit 7C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2293]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"9386","summary":null,"start":49187479,"end":49187670,"strand":-1,"description":"cytochrome c oxidase subunit 7C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2293]"}, {"versioned_ensembl_gene_id":"ENSG00000251329.1","gene_symbol":"LINC02353","gene_name":"long intergenic non-protein coding RNA 2353 [Source:HGNC Symbol;Acc:HGNC:53275]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927363","summary":null,"start":32351038,"end":32353220,"strand":1,"description":"long intergenic non-protein coding RNA 2353 [Source:HGNC Symbol;Acc:HGNC:53275]"}, {"versioned_ensembl_gene_id":"ENSG00000183666.16","gene_symbol":"GUSBP1","gene_name":"glucuronidase, beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13670]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728411","summary":null,"start":21341833,"end":21589372,"strand":1,"description":"glucuronidase, beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13670]"}, {"versioned_ensembl_gene_id":"ENSG00000283219.1","gene_symbol":"AC006160.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17557892,"end":17558045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221986.6","gene_symbol":"MYBPHL","gene_name":"myosin binding protein H like [Source:HGNC Symbol;Acc:HGNC:30434]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343263","summary":"This gene encodes a protein with two immunoglobulin superfamily domains and a fibronectin 3 domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":109292365,"end":109307041,"strand":-1,"description":"myosin binding protein H like [Source:HGNC Symbol;Acc:HGNC:30434]"}, {"versioned_ensembl_gene_id":"ENSG00000237609.1","gene_symbol":"AF064858.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39028536,"end":39029128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237721.1","gene_symbol":"AF064858.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39006648,"end":39011329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143786.7","gene_symbol":"CNIH3","gene_name":"cornichon family AMPA receptor auxiliary protein 3 [Source:HGNC Symbol;Acc:HGNC:26802]","synonyms":"FLJ38993,CNIH-3","biotype":"protein_coding","ncbi_id":"149111","summary":null,"start":224434660,"end":224740549,"strand":1,"description":"cornichon family AMPA receptor auxiliary protein 3 [Source:HGNC Symbol;Acc:HGNC:26802]"}, {"versioned_ensembl_gene_id":"ENSG00000233384.2","gene_symbol":"AC096537.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":224611404,"end":224616220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105723.11","gene_symbol":"GSK3A","gene_name":"glycogen synthase kinase 3 alpha [Source:HGNC Symbol;Acc:HGNC:4616]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2931","summary":"This gene encodes a multifunctional Ser/Thr protein kinase that is implicated in the control of several regulatory proteins including glycogen synthase, and transcription factors, such as JUN. It also plays a role in the WNT and PI3K signaling pathways, as well as regulates the production of beta-amyloid peptides associated with Alzheimer's disease. [provided by RefSeq, Oct 2011]","start":42230186,"end":42242625,"strand":-1,"description":"glycogen synthase kinase 3 alpha [Source:HGNC Symbol;Acc:HGNC:4616]"}, {"versioned_ensembl_gene_id":"ENSG00000233260.1","gene_symbol":"RPSAP63","gene_name":"ribosomal protein SA pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35581]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270755","summary":null,"start":133762796,"end":133763683,"strand":1,"description":"ribosomal protein SA pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35581]"}, {"versioned_ensembl_gene_id":"ENSG00000164221.12","gene_symbol":"CCDC112","gene_name":"coiled-coil domain containing 112 [Source:HGNC Symbol;Acc:HGNC:28599]","synonyms":"MGC39633","biotype":"protein_coding","ncbi_id":"153733","summary":null,"start":115267188,"end":115296831,"strand":-1,"description":"coiled-coil domain containing 112 [Source:HGNC Symbol;Acc:HGNC:28599]"}, {"versioned_ensembl_gene_id":"ENSG00000264596.1","gene_symbol":"AP000897.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7814118,"end":7815730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265413.1","gene_symbol":"AP001094.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8402847,"end":8405161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226435.10","gene_symbol":"ANKRD18DP","gene_name":"ankyrin repeat domain 18D, pseudogene [Source:HGNC Symbol;Acc:HGNC:28016]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"348840","summary":null,"start":198053522,"end":198080720,"strand":-1,"description":"ankyrin repeat domain 18D, pseudogene [Source:HGNC Symbol;Acc:HGNC:28016]"}, {"versioned_ensembl_gene_id":"ENSG00000206043.6","gene_symbol":"C18orf63","gene_name":"chromosome 18 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:40037]","synonyms":"DKFZP781G0119","biotype":"protein_coding","ncbi_id":"644041","summary":null,"start":74315813,"end":74359187,"strand":1,"description":"chromosome 18 open reading frame 63 [Source:HGNC Symbol;Acc:HGNC:40037]"}, {"versioned_ensembl_gene_id":"ENSG00000229165.1","gene_symbol":"GDI2P1","gene_name":"GDP dissociation inhibitor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4228]","synonyms":"GDI2P","biotype":"processed_pseudogene","ncbi_id":"2667","summary":null,"start":48902556,"end":48903891,"strand":-1,"description":"GDP dissociation inhibitor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4228]"}, {"versioned_ensembl_gene_id":"ENSG00000249553.1","gene_symbol":"PPP2R2B-IT1","gene_name":"PPP2R2B intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42984]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874361","summary":null,"start":146914207,"end":146919506,"strand":-1,"description":"PPP2R2B intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:42984]"}, {"versioned_ensembl_gene_id":"ENSG00000184788.12","gene_symbol":"SATL1","gene_name":"spermidine/spermine N1-acetyl transferase like 1 [Source:HGNC Symbol;Acc:HGNC:27992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340562","summary":null,"start":85092287,"end":85109048,"strand":-1,"description":"spermidine/spermine N1-acetyl transferase like 1 [Source:HGNC Symbol;Acc:HGNC:27992]"}, {"versioned_ensembl_gene_id":"ENSG00000187600.13","gene_symbol":"TMEM247","gene_name":"transmembrane protein 247 [Source:HGNC Symbol;Acc:HGNC:42967]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"388946","summary":null,"start":46429190,"end":46441833,"strand":1,"description":"transmembrane protein 247 [Source:HGNC Symbol;Acc:HGNC:42967]"}, {"versioned_ensembl_gene_id":"ENSG00000167117.8","gene_symbol":"LINC00483","gene_name":"long intergenic non-protein coding RNA 483 [Source:HGNC Symbol;Acc:HGNC:26080]","synonyms":"FLJ20694,C17orf73","biotype":"processed_transcript","ncbi_id":"55018","summary":null,"start":50761029,"end":50767557,"strand":-1,"description":"long intergenic non-protein coding RNA 483 [Source:HGNC Symbol;Acc:HGNC:26080]"}, {"versioned_ensembl_gene_id":"ENSG00000065328.16","gene_symbol":"MCM10","gene_name":"minichromosome maintenance 10 replication initiation factor [Source:HGNC Symbol;Acc:HGNC:18043]","synonyms":"PRO2249,DNA43,CNA43","biotype":"protein_coding","ncbi_id":"55388","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre-RC) and it may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein can interact with MCM2 and MCM6, as well as with the origin recognition protein ORC2. It is regulated by proteolysis and phosphorylation in a cell cycle-dependent manner. Studies of a similar protein in Xenopus suggest that the chromatin binding of this protein at the onset of DNA replication is after pre-RC assembly and before origin unwinding. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":13161554,"end":13211104,"strand":1,"description":"minichromosome maintenance 10 replication initiation factor [Source:HGNC Symbol;Acc:HGNC:18043]"}, {"versioned_ensembl_gene_id":"ENSG00000236700.5","gene_symbol":"LINC01010","gene_name":"long intergenic non-protein coding RNA 1010 [Source:HGNC Symbol;Acc:HGNC:48978]","synonyms":null,"biotype":"lincRNA","ncbi_id":"154092","summary":null,"start":134437716,"end":134504581,"strand":1,"description":"long intergenic non-protein coding RNA 1010 [Source:HGNC Symbol;Acc:HGNC:48978]"}, {"versioned_ensembl_gene_id":"ENSG00000227064.1","gene_symbol":"Z82205.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132907279,"end":132907575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167261.13","gene_symbol":"DPEP2","gene_name":"dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:23028]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64174","summary":"DPEP2 belongs to the membrane-bound dipeptidase (EC 3.4.13.19) family. These enzymes hydrolyze a variety of dipeptides, including leukotriene D4, the beta-lactam ring of some antibiotics, and cystinyl-bis-glycine (cys-bis-gly) formed during glutathione degradation (Habib et al., 2003 [PubMed 12738806]).[supplied by OMIM, Mar 2008]","start":67987394,"end":68000586,"strand":-1,"description":"dipeptidase 2 [Source:HGNC Symbol;Acc:HGNC:23028]"}, {"versioned_ensembl_gene_id":"ENSG00000263276.1","gene_symbol":"AC020978.8","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":68224713,"end":68227734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250240.5","gene_symbol":"AC008840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95701249,"end":95732295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101230.5","gene_symbol":"ISM1","gene_name":"isthmin 1 [Source:HGNC Symbol;Acc:HGNC:16213]","synonyms":"C20orf82,bA149I18.1","biotype":"protein_coding","ncbi_id":"140862","summary":null,"start":13221771,"end":13300651,"strand":1,"description":"isthmin 1 [Source:HGNC Symbol;Acc:HGNC:16213]"}, {"versioned_ensembl_gene_id":"ENSG00000135426.15","gene_symbol":"TESPA1","gene_name":"thymocyte expressed, positive selection associated 1 [Source:HGNC Symbol;Acc:HGNC:29109]","synonyms":"KIAA0748","biotype":"protein_coding","ncbi_id":"9840","summary":null,"start":54948018,"end":54984746,"strand":-1,"description":"thymocyte expressed, positive selection associated 1 [Source:HGNC Symbol;Acc:HGNC:29109]"}, {"versioned_ensembl_gene_id":"ENSG00000160299.16","gene_symbol":"PCNT","gene_name":"pericentrin [Source:HGNC Symbol;Acc:HGNC:16068]","synonyms":"SCKL4,PCNTB,PCNT2,PCN,KIAA0402,KEN","biotype":"protein_coding","ncbi_id":"5116","summary":"The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":46324122,"end":46445769,"strand":1,"description":"pericentrin [Source:HGNC Symbol;Acc:HGNC:16068]"}, {"versioned_ensembl_gene_id":"ENSG00000258883.1","gene_symbol":"AC068446.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21250180,"end":21260147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276422.1","gene_symbol":"AL590491.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60943311,"end":60964185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155545.19","gene_symbol":"MIER3","gene_name":"MIER family member 3 [Source:HGNC Symbol;Acc:HGNC:26678]","synonyms":"FLJ35954,DKFZp781I1119,DKFZp686L09111","biotype":"protein_coding","ncbi_id":"166968","summary":null,"start":56919602,"end":56971675,"strand":-1,"description":"MIER family member 3 [Source:HGNC Symbol;Acc:HGNC:26678]"}, {"versioned_ensembl_gene_id":"ENSG00000246089.3","gene_symbol":"AC016065.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6403551,"end":6407142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260007.2","gene_symbol":"AC107871.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":68184032,"end":68229718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276519.1","gene_symbol":"AC092142.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81987948,"end":81989016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260602.2","gene_symbol":"HMGN2P40","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39411]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874484","summary":null,"start":68254549,"end":68254939,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39411]"}, {"versioned_ensembl_gene_id":"ENSG00000085274.15","gene_symbol":"MYNN","gene_name":"myoneurin [Source:HGNC Symbol;Acc:HGNC:14955]","synonyms":"ZNF902,ZBTB31,SBBIZ1","biotype":"protein_coding","ncbi_id":"55892","summary":"This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010]","start":169772831,"end":169789716,"strand":1,"description":"myoneurin [Source:HGNC Symbol;Acc:HGNC:14955]"}, {"versioned_ensembl_gene_id":"ENSG00000102931.7","gene_symbol":"ARL2BP","gene_name":"ADP ribosylation factor like GTPase 2 binding protein [Source:HGNC Symbol;Acc:HGNC:17146]","synonyms":"RP66,BART1,BART","biotype":"protein_coding","ncbi_id":"23568","summary":"ADP-ribosylation factor (ARF)-like proteins (ARLs) comprise a functionally distinct group of the ARF family of RAS-related GTPases. The protein encoded by this gene binds to ARL2.GTP with high affinity but does not interact with ARL2.GDP, activated ARF, or RHO proteins. The lack of detectable membrane association of this protein or ARL2 upon activation of ARL2 is suggestive of actions distinct from those of the ARFs. This protein is considered to be the first ARL2-specific effector identified, due to its interaction with ARL2.GTP but lack of ARL2 GTPase-activating protein activity. [provided by RefSeq, Jul 2008]","start":57245098,"end":57253635,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein [Source:HGNC Symbol;Acc:HGNC:17146]"}, {"versioned_ensembl_gene_id":"ENSG00000169019.10","gene_symbol":"COMMD8","gene_name":"COMM domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26036]","synonyms":"FLJ20502","biotype":"protein_coding","ncbi_id":"54951","summary":"The protein encoded by this gene binds coiled-coil domain-containing protein 22 (CCDC22), and this complex can regulate the turnover of I-kappa-B and the activation of NF-kappa-B. [provided by RefSeq, Jul 2016]","start":47450796,"end":47463719,"strand":-1,"description":"COMM domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26036]"}, {"versioned_ensembl_gene_id":"ENSG00000255005.1","gene_symbol":"AP003128.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85916502,"end":85923682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278743.1","gene_symbol":"AC087239.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25385670,"end":25386241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239345.2","gene_symbol":"HNRNPA1P26","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"664722","summary":null,"start":100855288,"end":100856379,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39544]"}, {"versioned_ensembl_gene_id":"ENSG00000229339.1","gene_symbol":"AC093414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42051181,"end":42051694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231549.1","gene_symbol":"USMG5P1","gene_name":"USMG5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31716]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288307","summary":null,"start":74173890,"end":74174066,"strand":1,"description":"USMG5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31716]"}, {"versioned_ensembl_gene_id":"ENSG00000112799.8","gene_symbol":"LY86","gene_name":"lymphocyte antigen 86 [Source:HGNC Symbol;Acc:HGNC:16837]","synonyms":"MD-1,dJ80N2.1","biotype":"protein_coding","ncbi_id":"9450","summary":null,"start":6588108,"end":6654983,"strand":1,"description":"lymphocyte antigen 86 [Source:HGNC Symbol;Acc:HGNC:16837]"}, {"versioned_ensembl_gene_id":"ENSG00000248482.1","gene_symbol":"AC008406.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135124380,"end":135131249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234969.1","gene_symbol":"AL627389.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74069276,"end":74070832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130204.12","gene_symbol":"TOMM40","gene_name":"translocase of outer mitochondrial membrane 40 [Source:HGNC Symbol;Acc:HGNC:18001]","synonyms":"TOM40,PEREC1,PER-EC1,D19S1177E,C19orf1","biotype":"protein_coding","ncbi_id":"10452","summary":"The protein encoded by this gene is localized in the outer membrane of the mitochondria. It is the channel-forming subunit of the translocase of the mitochondrial outer membrane (TOM) complex that is essential for import of protein precursors into mitochondria. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]","start":44890569,"end":44903689,"strand":1,"description":"translocase of outer mitochondrial membrane 40 [Source:HGNC Symbol;Acc:HGNC:18001]"}, {"versioned_ensembl_gene_id":"ENSG00000088881.20","gene_symbol":"EBF4","gene_name":"early B-cell factor 4 [Source:HGNC Symbol;Acc:HGNC:29278]","synonyms":"RP5-860F19.3,O/E-4,KIAA1442,COE4","biotype":"protein_coding","ncbi_id":"57593","summary":"EBF4 belongs to the conserved Olf/EBF family of helix-loop-helix transcription factors, members of which play important roles in neural development and B-cell maturation (Wang et al., 2002 [PubMed 12139918]).[supplied by OMIM, Mar 2008]","start":2692878,"end":2760108,"strand":1,"description":"early B-cell factor 4 [Source:HGNC Symbol;Acc:HGNC:29278]"}, {"versioned_ensembl_gene_id":"ENSG00000219298.1","gene_symbol":"AL355497.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149977471,"end":149979105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162782.15","gene_symbol":"TDRD5","gene_name":"tudor domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20614]","synonyms":"TUDOR3,FLJ34823","biotype":"protein_coding","ncbi_id":"163589","summary":null,"start":179591613,"end":179691272,"strand":1,"description":"tudor domain containing 5 [Source:HGNC Symbol;Acc:HGNC:20614]"}, {"versioned_ensembl_gene_id":"ENSG00000105193.8","gene_symbol":"RPS16","gene_name":"ribosomal protein S16 [Source:HGNC Symbol;Acc:HGNC:10396]","synonyms":"S16","biotype":"protein_coding","ncbi_id":"6217","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S9P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":39433207,"end":39435948,"strand":-1,"description":"ribosomal protein S16 [Source:HGNC Symbol;Acc:HGNC:10396]"}, {"versioned_ensembl_gene_id":"ENSG00000116675.15","gene_symbol":"DNAJC6","gene_name":"DnaJ heat shock protein family (Hsp40) member C6 [Source:HGNC Symbol;Acc:HGNC:15469]","synonyms":"PARK19,KIAA0473","biotype":"protein_coding","ncbi_id":"9829","summary":"DNAJC6 belongs to the evolutionarily conserved DNAJ/HSP40 family of proteins, which regulate molecular chaperone activity by stimulating ATPase activity. DNAJ proteins may have up to 3 distinct domains: a conserved 70-amino acid J domain, usually at the N terminus, a glycine/phenylalanine (G/F)-rich region, and a cysteine-rich domain containing 4 motifs resembling a zinc finger domain (Ohtsuka and Hata, 2000 [PubMed 11147971]).[supplied by OMIM, Mar 2008]","start":65248219,"end":65415869,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C6 [Source:HGNC Symbol;Acc:HGNC:15469]"}, {"versioned_ensembl_gene_id":"ENSG00000223742.1","gene_symbol":"AC112495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28571532,"end":28586395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231480.1","gene_symbol":"SNRPGP13","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39332]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874428","summary":null,"start":38502445,"end":38502621,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39332]"}, {"versioned_ensembl_gene_id":"ENSG00000273238.2","gene_symbol":"AC116565.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":573880,"end":576300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230720.1","gene_symbol":"AL451107.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30723251,"end":30723740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135336.14","gene_symbol":"ORC3","gene_name":"origin recognition complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:8489]","synonyms":"IMAGE50150,ORC3L,LATHEO","biotype":"protein_coding","ncbi_id":"23595","summary":"The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Studies of a similar gene in Drosophila suggested a possible role of this protein in neuronal proliferation and olfactory memory. Alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene. [provided by RefSeq, Jul 2008]","start":87590067,"end":87667453,"strand":1,"description":"origin recognition complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:8489]"}, {"versioned_ensembl_gene_id":"ENSG00000234742.1","gene_symbol":"AC144530.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197850400,"end":197850954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258710.7","gene_symbol":"LINC01193","gene_name":"long intergenic non-protein coding RNA 1193 [Source:HGNC Symbol;Acc:HGNC:28003]","synonyms":"LOC348120,CT60","biotype":"lincRNA","ncbi_id":"348120","summary":null,"start":20940438,"end":20993303,"strand":1,"description":"long intergenic non-protein coding RNA 1193 [Source:HGNC Symbol;Acc:HGNC:28003]"}, {"versioned_ensembl_gene_id":"ENSG00000023445.13","gene_symbol":"BIRC3","gene_name":"baculoviral IAP repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:591]","synonyms":"RNF49,MIHC,MALT2,hiap-1,cIAP2,c-IAP2,API2","biotype":"protein_coding","ncbi_id":"330","summary":"This gene encodes a member of the IAP family of proteins that inhibit apoptosis by binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2, probably by interfering with activation of ICE-like proteases. The encoded protein inhibits apoptosis induced by serum deprivation but does not affect apoptosis resulting from exposure to menadione, a potent inducer of free radicals. It contains 3 baculovirus IAP repeats and a ring finger domain. Transcript variants encoding the same isoform have been identified. [provided by RefSeq, Aug 2011]","start":102317450,"end":102339403,"strand":1,"description":"baculoviral IAP repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:591]"}, {"versioned_ensembl_gene_id":"ENSG00000242816.1","gene_symbol":"AC092691.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117790673,"end":117793765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232675.7","gene_symbol":"AL121830.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19693209,"end":19697576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237214.3","gene_symbol":"AL080243.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41064052,"end":41064633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279461.2","gene_symbol":"AC005480.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74003396,"end":74003470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284356.1","gene_symbol":"AC233724.20","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17597232,"end":17597828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279051.4","gene_symbol":"OR6Q1","gene_name":"olfactory receptor family 6 subfamily Q member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15302]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219952","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":58030930,"end":58031931,"strand":1,"description":"olfactory receptor family 6 subfamily Q member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15302]"}, {"versioned_ensembl_gene_id":"ENSG00000274949.1","gene_symbol":"AL109804.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":3811384,"end":3823882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255462.1","gene_symbol":"AC104031.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11570084,"end":11573782,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233048.1","gene_symbol":"LINC01722","gene_name":"long intergenic non-protein coding RNA 1722 [Source:HGNC Symbol;Acc:HGNC:52510]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929486","summary":null,"start":12865202,"end":12952519,"strand":-1,"description":"long intergenic non-protein coding RNA 1722 [Source:HGNC Symbol;Acc:HGNC:52510]"}, {"versioned_ensembl_gene_id":"ENSG00000279081.2","gene_symbol":"AL356585.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18206570,"end":18207466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229091.3","gene_symbol":"HSPA8P8","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287551","summary":null,"start":10451311,"end":10453252,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:44923]"}, {"versioned_ensembl_gene_id":"ENSG00000254749.1","gene_symbol":"OR5BD1P","gene_name":"olfactory receptor family 5 subfamily BD member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14843]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79483","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57945598,"end":57946414,"strand":-1,"description":"olfactory receptor family 5 subfamily BD member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14843]"}, {"versioned_ensembl_gene_id":"ENSG00000163060.7","gene_symbol":"TEKT4","gene_name":"tektin 4 [Source:HGNC Symbol;Acc:HGNC:31012]","synonyms":"MGC27019","biotype":"protein_coding","ncbi_id":"150483","summary":null,"start":94871433,"end":94876829,"strand":1,"description":"tektin 4 [Source:HGNC Symbol;Acc:HGNC:31012]"}, {"versioned_ensembl_gene_id":"ENSG00000225217.1","gene_symbol":"HSPA7","gene_name":"heat shock protein family A (Hsp70) member 7 [Source:HGNC Symbol;Acc:HGNC:5240]","synonyms":"HSP70B","biotype":"unprocessed_pseudogene","ncbi_id":"3311","summary":null,"start":161606291,"end":161608217,"strand":1,"description":"heat shock protein family A (Hsp70) member 7 [Source:HGNC Symbol;Acc:HGNC:5240]"}, {"versioned_ensembl_gene_id":"ENSG00000235489.4","gene_symbol":"DBF4P1","gene_name":"DBF4 zinc finger pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45059]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645084","summary":null,"start":64168959,"end":64170850,"strand":-1,"description":"DBF4 zinc finger pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45059]"}, {"versioned_ensembl_gene_id":"ENSG00000277598.1","gene_symbol":"BX088702.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60546920,"end":60547154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256053.7","gene_symbol":"APOPT1","gene_name":"apoptogenic 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:20492]","synonyms":"MGC2562,C14orf153,APOP-1","biotype":"protein_coding","ncbi_id":"84334","summary":"This gene encodes a protein that localizes to the mitochondria, where it stimulates the release of cytochrome c, thereby promoting programmed cell death. Mutations in this gene have been found in individuals with mitochondrial complex IV deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":103562962,"end":103607523,"strand":1,"description":"apoptogenic 1, mitochondrial [Source:HGNC Symbol;Acc:HGNC:20492]"}, {"versioned_ensembl_gene_id":"ENSG00000226426.1","gene_symbol":"AC012558.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64036345,"end":64037280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235098.8","gene_symbol":"ANKRD65","gene_name":"ankyrin repeat domain 65 [Source:HGNC Symbol;Acc:HGNC:42950]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441869","summary":null,"start":1418420,"end":1421769,"strand":-1,"description":"ankyrin repeat domain 65 [Source:HGNC Symbol;Acc:HGNC:42950]"}, {"versioned_ensembl_gene_id":"ENSG00000164129.11","gene_symbol":"NPY5R","gene_name":"neuropeptide Y receptor Y5 [Source:HGNC Symbol;Acc:HGNC:7958]","synonyms":"NPYR5","biotype":"protein_coding","ncbi_id":"4889","summary":"The protein encoded by this gene is a receptor for neuropeptide Y and peptide YY. The encoded protein appears to be involved in regulating food intake, with defects in this gene being associated with eating disorders. Also, the encoded protein is involved in a pathway that protects neuroblastoma cells from chemotherapy-induced cell death, providing a possible therapeutic target against neuroblastoma. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015]","start":163343939,"end":163351934,"strand":1,"description":"neuropeptide Y receptor Y5 [Source:HGNC Symbol;Acc:HGNC:7958]"}, {"versioned_ensembl_gene_id":"ENSG00000225905.1","gene_symbol":"AL391244.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1420245,"end":1422691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114021.11","gene_symbol":"NIT2","gene_name":"nitrilase family member 2 [Source:HGNC Symbol;Acc:HGNC:29878]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56954","summary":null,"start":100334701,"end":100361635,"strand":1,"description":"nitrilase family member 2 [Source:HGNC Symbol;Acc:HGNC:29878]"}, {"versioned_ensembl_gene_id":"ENSG00000254401.1","gene_symbol":"AC111188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11117854,"end":11183611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275320.1","gene_symbol":"Z95327.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100815865,"end":100817174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278642.1","gene_symbol":"AC015813.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57955965,"end":57956143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216844.1","gene_symbol":"AC009494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20843256,"end":20843710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203705.10","gene_symbol":"TATDN3","gene_name":"TatD DNase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:27010]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128387","summary":null,"start":212791828,"end":212816626,"strand":1,"description":"TatD DNase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:27010]"}, {"versioned_ensembl_gene_id":"ENSG00000257649.1","gene_symbol":"METTL7AP1","gene_name":"methyltransferase like 7A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48874]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996686","summary":null,"start":52229093,"end":52229588,"strand":-1,"description":"methyltransferase like 7A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48874]"}, {"versioned_ensembl_gene_id":"ENSG00000144455.13","gene_symbol":"SUMF1","gene_name":"sulfatase modifying factor 1 [Source:HGNC Symbol;Acc:HGNC:20376]","synonyms":"UNQ3037,FGE","biotype":"protein_coding","ncbi_id":"285362","summary":"This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":3700814,"end":4467281,"strand":-1,"description":"sulfatase modifying factor 1 [Source:HGNC Symbol;Acc:HGNC:20376]"}, {"versioned_ensembl_gene_id":"ENSG00000176771.16","gene_symbol":"NCKAP5","gene_name":"NCK associated protein 5 [Source:HGNC Symbol;Acc:HGNC:29847]","synonyms":"NAP5,ERIH2,ERIH1","biotype":"protein_coding","ncbi_id":"344148","summary":null,"start":132671799,"end":133568463,"strand":-1,"description":"NCK associated protein 5 [Source:HGNC Symbol;Acc:HGNC:29847]"}, {"versioned_ensembl_gene_id":"ENSG00000268391.1","gene_symbol":"MTCO3P42","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52145]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075189","summary":null,"start":49548918,"end":49549435,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52145]"}, {"versioned_ensembl_gene_id":"ENSG00000213066.11","gene_symbol":"FGFR1OP","gene_name":"FGFR1 oncogene partner [Source:HGNC Symbol;Acc:HGNC:17012]","synonyms":"FOP","biotype":"protein_coding","ncbi_id":"11116","summary":"This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. Alterations in this gene may also be associated with Crohn's disease, Graves' disease, and vitiligo. Alternatively spliced transcript variants that encode different proteins have been identified. [provided by RefSeq, Jul 2013]","start":166999182,"end":167052713,"strand":1,"description":"FGFR1 oncogene partner [Source:HGNC Symbol;Acc:HGNC:17012]"}, {"versioned_ensembl_gene_id":"ENSG00000218426.5","gene_symbol":"AL590867.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153282287,"end":153282733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265542.5","gene_symbol":"AC015845.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57771946,"end":57834749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196639.6","gene_symbol":"HRH1","gene_name":"histamine receptor H1 [Source:HGNC Symbol;Acc:HGNC:5182]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3269","summary":"Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. Its various actions are mediated by histamine receptors H1, H2, H3 and H4. The protein encoded by this gene is an integral membrane protein and belongs to the G protein-coupled receptor superfamily. It mediates the contraction of smooth muscles, the increase in capillary permeability due to contraction of terminal venules, the release of catecholamine from adrenal medulla, and neurotransmission in the central nervous system. It has been associated with multiple processes, including memory and learning, circadian rhythm, and thermoregulation. It is also known to contribute to the pathophysiology of allergic diseases such as atopic dermatitis, asthma, anaphylaxis and allergic rhinitis. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2015]","start":11137093,"end":11263557,"strand":1,"description":"histamine receptor H1 [Source:HGNC Symbol;Acc:HGNC:5182]"}, {"versioned_ensembl_gene_id":"ENSG00000169359.13","gene_symbol":"SLC33A1","gene_name":"solute carrier family 33 member 1 [Source:HGNC Symbol;Acc:HGNC:95]","synonyms":"SPG42,AT1,AT-1,ACATN","biotype":"protein_coding","ncbi_id":"9197","summary":"The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]","start":155821024,"end":155854429,"strand":-1,"description":"solute carrier family 33 member 1 [Source:HGNC Symbol;Acc:HGNC:95]"}, {"versioned_ensembl_gene_id":"ENSG00000165078.12","gene_symbol":"CPA6","gene_name":"carboxypeptidase A6 [Source:HGNC Symbol;Acc:HGNC:17245]","synonyms":"CPAH","biotype":"protein_coding","ncbi_id":"57094","summary":"The gene encodes a member of the peptidase M14 family of metallocarboxypeptidases. The encoded preproprotein is proteolytically processed to generate the mature enzyme, which catalyzes the release of large hydrophobic C-terminal amino acids. This enzyme has functions ranging from digestion of food to selective biosynthesis of neuroendocrine peptides. Mutations in this gene may be linked to epilepsy and febrile seizures, and a translocation t(6;8)(q26;q13) involving this gene has been associated with Duane retraction syndrome. [provided by RefSeq, May 2016]","start":67422038,"end":67746385,"strand":-1,"description":"carboxypeptidase A6 [Source:HGNC Symbol;Acc:HGNC:17245]"}, {"versioned_ensembl_gene_id":"ENSG00000255130.1","gene_symbol":"AC022874.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67732587,"end":67735665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158887.15","gene_symbol":"MPZ","gene_name":"myelin protein zero [Source:HGNC Symbol;Acc:HGNC:7225]","synonyms":"HMSNIB,CMT2J,CMT2I,CMT1B,CMT1","biotype":"protein_coding","ncbi_id":"4359","summary":"This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2015]","start":161304735,"end":161309972,"strand":-1,"description":"myelin protein zero [Source:HGNC Symbol;Acc:HGNC:7225]"}, {"versioned_ensembl_gene_id":"ENSG00000250474.2","gene_symbol":"WBP1LP2","gene_name":"WW domain binding protein 1-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43949]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506330","summary":null,"start":107628553,"end":107629550,"strand":1,"description":"WW domain binding protein 1-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43949]"}, {"versioned_ensembl_gene_id":"ENSG00000218631.1","gene_symbol":"AL117344.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157372556,"end":157373171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213078.3","gene_symbol":"AL390955.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157365990,"end":157366923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148120.16","gene_symbol":"C9orf3","gene_name":"chromosome 9 open reading frame 3 [Source:HGNC Symbol;Acc:HGNC:1361]","synonyms":"FLJ14675,C90RF3,APO,AP-O,AOPEP","biotype":"protein_coding","ncbi_id":"84909","summary":"This gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc-dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]","start":94726701,"end":95087218,"strand":1,"description":"chromosome 9 open reading frame 3 [Source:HGNC Symbol;Acc:HGNC:1361]"}, {"versioned_ensembl_gene_id":"ENSG00000183840.6","gene_symbol":"GPR39","gene_name":"G protein-coupled receptor 39 [Source:HGNC Symbol;Acc:HGNC:4496]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2863","summary":"This gene is a member of the ghrelin receptor family and encodes a rhodopsin-type G-protein-coupled receptor (GPCR). The encoded protein is involved in zinc-dependent signaling in epithelial tissue in intestines, prostate and salivary glands. The protein may also be involved in the pathophysiology of depression. [provided by RefSeq, Jun 2016]","start":132416574,"end":132646559,"strand":1,"description":"G protein-coupled receptor 39 [Source:HGNC Symbol;Acc:HGNC:4496]"}, {"versioned_ensembl_gene_id":"ENSG00000165929.12","gene_symbol":"TC2N","gene_name":"tandem C2 domains, nuclear [Source:HGNC Symbol;Acc:HGNC:19859]","synonyms":"C14orf47,Tac2-N,MTAC2D1,FLJ36557,C2CD1","biotype":"protein_coding","ncbi_id":"123036","summary":null,"start":91779751,"end":91867536,"strand":-1,"description":"tandem C2 domains, nuclear [Source:HGNC Symbol;Acc:HGNC:19859]"}, {"versioned_ensembl_gene_id":"ENSG00000230065.1","gene_symbol":"AC010974.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132660526,"end":132666990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187893.10","gene_symbol":"CXXC1P1","gene_name":"CXXC finger protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27864]","synonyms":"NCRNA00236,FLJ36789,CXorf25","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"392459","summary":null,"start":47707191,"end":47753456,"strand":1,"description":"CXXC finger protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27864]"}, {"versioned_ensembl_gene_id":"ENSG00000205037.2","gene_symbol":"AC134312.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88088041,"end":88100985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260166.1","gene_symbol":"AC134312.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88087387,"end":88087932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262980.1","gene_symbol":"OR52L2P","gene_name":"olfactory receptor family 52 subfamily L member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14788]","synonyms":"OR52L2","biotype":"unprocessed_pseudogene","ncbi_id":"79274","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6057316,"end":6058275,"strand":-1,"description":"olfactory receptor family 52 subfamily L member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14788]"}, {"versioned_ensembl_gene_id":"ENSG00000185291.11","gene_symbol":"IL3RA","gene_name":"interleukin 3 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6012]","synonyms":"CD123","biotype":"protein_coding","ncbi_id":"3563","summary":"The protein encoded by this gene is an interleukin 3 specific subunit of a heterodimeric cytokine receptor. The receptor is comprised of a ligand specific alpha subunit and a signal transducing beta subunit shared by the receptors for interleukin 3 (IL3), colony stimulating factor 2 (CSF2/GM-CSF), and interleukin 5 (IL5). The binding of this protein to IL3 depends on the beta subunit. The beta subunit is activated by the ligand binding, and is required for the biological activities of IL3. This gene and the gene encoding the colony stimulating factor 2 receptor alpha chain (CSF2RA) form a cytokine receptor gene cluster in a X-Y pseudoautosomal region on chromosomes X or Y. Alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jun 2012]","start":1336616,"end":1382689,"strand":1,"description":"interleukin 3 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6012]"}, {"versioned_ensembl_gene_id":"ENSG00000175826.11","gene_symbol":"CTDNEP1","gene_name":"CTD nuclear envelope phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:19085]","synonyms":"NET56,HSA011916,DULLARD","biotype":"protein_coding","ncbi_id":"23399","summary":null,"start":7243591,"end":7252491,"strand":-1,"description":"CTD nuclear envelope phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:19085]"}, {"versioned_ensembl_gene_id":"ENSG00000280028.1","gene_symbol":"AC007431.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57531769,"end":57532355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167664.8","gene_symbol":"TMIGD2","gene_name":"transmembrane and immunoglobulin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28324]","synonyms":"MGC23244,IGPR-1,CD28H","biotype":"protein_coding","ncbi_id":"126259","summary":null,"start":4292232,"end":4302431,"strand":-1,"description":"transmembrane and immunoglobulin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28324]"}, {"versioned_ensembl_gene_id":"ENSG00000251056.1","gene_symbol":"ANKRD20A17P","gene_name":"ankyrin repeat domain 20 family member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:43608]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421363","summary":null,"start":49502145,"end":49506022,"strand":-1,"description":"ankyrin repeat domain 20 family member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:43608]"}, {"versioned_ensembl_gene_id":"ENSG00000143569.18","gene_symbol":"UBAP2L","gene_name":"ubiquitin associated protein 2 like [Source:HGNC Symbol;Acc:HGNC:29877]","synonyms":"NICE-4,KIAA0144","biotype":"protein_coding","ncbi_id":"9898","summary":null,"start":154220179,"end":154271510,"strand":1,"description":"ubiquitin associated protein 2 like [Source:HGNC Symbol;Acc:HGNC:29877]"}, {"versioned_ensembl_gene_id":"ENSG00000263212.2","gene_symbol":"AC004224.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":3458071,"end":3515564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197442.9","gene_symbol":"MAP3K5","gene_name":"mitogen-activated protein kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6857]","synonyms":"ASK1,MEKK5,MAPKKK5","biotype":"protein_coding","ncbi_id":"4217","summary":"Mitogen-activated protein kinase (MAPK) signaling cascades include MAPK or extracellular signal-regulated kinase (ERK), MAPK kinase (MKK or MEK), and MAPK kinase kinase (MAPKKK or MEKK). MAPKK kinase/MEKK phosphorylates and activates its downstream protein kinase, MAPK kinase/MEK, which in turn activates MAPK. The kinases of these signaling cascades are highly conserved, and homologs exist in yeast, Drosophila, and mammalian cells. MAPKKK5 contains 1,374 amino acids with all 11 kinase subdomains. Northern blot analysis shows that MAPKKK5 transcript is abundantly expressed in human heart and pancreas. The MAPKKK5 protein phosphorylates and activates MKK4 (aliases SERK1, MAPKK4) in vitro, and activates c-Jun N-terminal kinase (JNK)/stress-activated protein kinase (SAPK) during transient expression in COS and 293 cells; MAPKKK5 does not activate MAPK/ERK. [provided by RefSeq, Jul 2008]","start":136557047,"end":136792518,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6857]"}, {"versioned_ensembl_gene_id":"ENSG00000234263.1","gene_symbol":"AL024508.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136629172,"end":136647999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237466.1","gene_symbol":"MTCO3P41","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52144]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075288","summary":null,"start":67628022,"end":67628349,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:52144]"}, {"versioned_ensembl_gene_id":"ENSG00000228318.3","gene_symbol":"AP001610.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41441056,"end":41445708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179091.4","gene_symbol":"CYC1","gene_name":"cytochrome c1 [Source:HGNC Symbol;Acc:HGNC:2579]","synonyms":"UQCR4","biotype":"protein_coding","ncbi_id":"1537","summary":"This gene encodes a subunit of the cytochrome bc1 complex, which plays an important role in the mitochondrial respiratory chain by transferring electrons from the Rieske iron-sulfur protein to cytochrome c. Mutations in this gene may cause mitochondrial complex III deficiency, nuclear type 6. [provided by RefSeq, Dec 2013]","start":144095027,"end":144097525,"strand":1,"description":"cytochrome c1 [Source:HGNC Symbol;Acc:HGNC:2579]"}, {"versioned_ensembl_gene_id":"ENSG00000076864.19","gene_symbol":"RAP1GAP","gene_name":"RAP1 GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:9858]","synonyms":"RAP1GAPII,RAP1GAP1,RAP1GA1,KIAA0474","biotype":"protein_coding","ncbi_id":"5909","summary":"This gene encodes a type of GTPase-activating-protein (GAP) that down-regulates the activity of the ras-related RAP1 protein. RAP1 acts as a molecular switch by cycling between an inactive GDP-bound form and an active GTP-bound form. The product of this gene, RAP1GAP, promotes the hydrolysis of bound GTP and hence returns RAP1 to the inactive state whereas other proteins, guanine nucleotide exchange factors (GEFs), act as RAP1 activators by facilitating the conversion of RAP1 from the GDP- to the GTP-bound form. In general, ras subfamily proteins, such as RAP1, play key roles in receptor-linked signaling pathways that control cell growth and differentiation. RAP1 plays a role in diverse processes such as cell proliferation, adhesion, differentiation, and embryogenesis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Aug 2011]","start":21596215,"end":21669363,"strand":-1,"description":"RAP1 GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:9858]"}, {"versioned_ensembl_gene_id":"ENSG00000220734.1","gene_symbol":"AL157823.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35765908,"end":35766927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228503.1","gene_symbol":"AL357558.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47958022,"end":47958603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223892.1","gene_symbol":"CR759763.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30084584,"end":30085579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273508.1","gene_symbol":"OR2T1","gene_name":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]","synonyms":"OR1-25","biotype":"protein_coding","ncbi_id":"26696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248408227,"end":248409336,"strand":1,"description":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]"}, {"versioned_ensembl_gene_id":"ENSG00000146083.11","gene_symbol":"RNF44","gene_name":"ring finger protein 44 [Source:HGNC Symbol;Acc:HGNC:19180]","synonyms":"KIAA1100","biotype":"protein_coding","ncbi_id":"22838","summary":"The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008]","start":176526697,"end":176538025,"strand":-1,"description":"ring finger protein 44 [Source:HGNC Symbol;Acc:HGNC:19180]"}, {"versioned_ensembl_gene_id":"ENSG00000244157.1","gene_symbol":"EIF4E2P2","gene_name":"eukaryotic translation initiation factor 4E family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51464]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645207","summary":null,"start":115279125,"end":115279860,"strand":1,"description":"eukaryotic translation initiation factor 4E family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51464]"}, {"versioned_ensembl_gene_id":"ENSG00000278659.1","gene_symbol":"OR2T6","gene_name":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]","synonyms":"OST703,OR2T9,OR2T6P","biotype":"protein_coding","ncbi_id":"254879","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248387949,"end":248388875,"strand":1,"description":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]"}, {"versioned_ensembl_gene_id":"ENSG00000268205.1","gene_symbol":"AC005261.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57304305,"end":57308562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268723.1","gene_symbol":"AC005261.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57317208,"end":57317562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261007.2","gene_symbol":"AC074051.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5365797,"end":5366688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148110.15","gene_symbol":"MFSD14B","gene_name":"major facilitator superfamily domain containing 14B [Source:HGNC Symbol;Acc:HGNC:23376]","synonyms":"HIATL1,FLJ14753","biotype":"protein_coding","ncbi_id":"84641","summary":null,"start":94374551,"end":94461042,"strand":1,"description":"major facilitator superfamily domain containing 14B [Source:HGNC Symbol;Acc:HGNC:23376]"}, {"versioned_ensembl_gene_id":"ENSG00000237256.1","gene_symbol":"PGAM3P","gene_name":"phosphoglycerate mutase 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16557]","synonyms":"dJ1128N12.1","biotype":"processed_pseudogene","ncbi_id":"170535","summary":null,"start":11621051,"end":11621477,"strand":1,"description":"phosphoglycerate mutase 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16557]"}, {"versioned_ensembl_gene_id":"ENSG00000270011.6","gene_symbol":"ZNF559-ZNF177","gene_name":"ZNF559-ZNF177 readthrough [Source:HGNC Symbol;Acc:HGNC:42964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529215","summary":"This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 559 (ZNF559) and zinc finger protein 177 (ZNF177) genes on chromosome 19. Alternative splicing results in multiple transcript variants, which encode the ZNF177 protein due to either leaky scanning by ribosomes, or absence of the ZNF559 start codon. [provided by RefSeq, Jan 2011]","start":9324174,"end":9382617,"strand":1,"description":"ZNF559-ZNF177 readthrough [Source:HGNC Symbol;Acc:HGNC:42964]"}, {"versioned_ensembl_gene_id":"ENSG00000223703.1","gene_symbol":"AC027612.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91736726,"end":91767439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184029.9","gene_symbol":"DSCR4","gene_name":"Down syndrome critical region 4 [Source:HGNC Symbol;Acc:HGNC:3045]","synonyms":"DCRB","biotype":"protein_coding","ncbi_id":"10281","summary":"The gene is found in a region of chromosome 21 that has been linked to the pathogenesis of Down syndrome. This gene is transcribed from a bi-directional promoter located in an endogenous retrovirus. [provided by RefSeq, Jan 2015]","start":37951425,"end":38121360,"strand":-1,"description":"Down syndrome critical region 4 [Source:HGNC Symbol;Acc:HGNC:3045]"}, {"versioned_ensembl_gene_id":"ENSG00000276975.2","gene_symbol":"HYDIN2","gene_name":"HYDIN2, axonemal central pair apparatus protein (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33129]","synonyms":"HYDINP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288805","summary":null,"start":146547367,"end":146914294,"strand":1,"description":"HYDIN2, axonemal central pair apparatus protein (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33129]"}, {"versioned_ensembl_gene_id":"ENSG00000223409.1","gene_symbol":"RPL17P17","gene_name":"ribosomal protein L17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35515]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270943","summary":null,"start":65843890,"end":65844446,"strand":1,"description":"ribosomal protein L17 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35515]"}, {"versioned_ensembl_gene_id":"ENSG00000226681.1","gene_symbol":"AC020595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181422154,"end":181425749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254777.5","gene_symbol":"AC022182.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60910053,"end":60966557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250392.2","gene_symbol":"LINC02502","gene_name":"long intergenic non-protein coding RNA 2502 [Source:HGNC Symbol;Acc:HGNC:53491]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996694","summary":null,"start":119939540,"end":119964293,"strand":1,"description":"long intergenic non-protein coding RNA 2502 [Source:HGNC Symbol;Acc:HGNC:53491]"}, {"versioned_ensembl_gene_id":"ENSG00000262312.2","gene_symbol":"AC004494.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3542739,"end":3545785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211720.3","gene_symbol":"TRBV11-1","gene_name":"T-cell receptor beta variable 11-1 [Source:HGNC Symbol;Acc:HGNC:12180]","synonyms":"TRBV111,TCRBV21S1,TCRBV11S1","biotype":"TR_V_gene","ncbi_id":"28582","summary":null,"start":142407672,"end":142408136,"strand":1,"description":"T-cell receptor beta variable 11-1 [Source:HGNC Symbol;Acc:HGNC:12180]"}, {"versioned_ensembl_gene_id":"ENSG00000232909.1","gene_symbol":"AL157823.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35733867,"end":35736947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268654.1","gene_symbol":"MIMT1","gene_name":"MER1 repeat containing imprinted transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33464]","synonyms":"MIM1,LINC00067,NCRNA00067","biotype":"lincRNA","ncbi_id":"100073347","summary":null,"start":56840902,"end":56848556,"strand":1,"description":"MER1 repeat containing imprinted transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33464]"}, {"versioned_ensembl_gene_id":"ENSG00000237604.1","gene_symbol":"AP001056.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44175489,"end":44176453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235171.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32283008,"end":32283967,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000253423.1","gene_symbol":"AC090132.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83200952,"end":83202431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157601.13","gene_symbol":"MX1","gene_name":"MX dynamin like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:7532]","synonyms":"IFI-78K,MxA","biotype":"protein_coding","ncbi_id":"4599","summary":"This gene encodes a guanosine triphosphate (GTP)-metabolizing protein that participates in the cellular antiviral response. The encoded protein is induced by type I and type II interferons and antagonizes the replication process of several different RNA and DNA viruses. There is a related gene located adjacent to this gene on chromosome 21, and there are multiple pseudogenes located in a cluster on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":41420304,"end":41459214,"strand":1,"description":"MX dynamin like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:7532]"}, {"versioned_ensembl_gene_id":"ENSG00000249837.1","gene_symbol":"AC121154.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124149377,"end":124252044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178795.9","gene_symbol":"GDPD4","gene_name":"glycerophosphodiester phosphodiesterase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24849]","synonyms":"GDE6","biotype":"protein_coding","ncbi_id":"220032","summary":null,"start":77216558,"end":77301687,"strand":-1,"description":"glycerophosphodiester phosphodiesterase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24849]"}, {"versioned_ensembl_gene_id":"ENSG00000258524.1","gene_symbol":"NT5CP1","gene_name":"5',3'-nucleotidase, cytosolic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20046]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326609","summary":null,"start":73571159,"end":73571667,"strand":-1,"description":"5',3'-nucleotidase, cytosolic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20046]"}, {"versioned_ensembl_gene_id":"ENSG00000271100.1","gene_symbol":"AP000753.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63698596,"end":63698764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149656.8","gene_symbol":"LINC00266-1","gene_name":"long intergenic non-protein coding RNA 266-1 [Source:HGNC Symbol;Acc:HGNC:16202]","synonyms":"NCRNA00266-1,NCRNA00266,C20orf69,bA476I15.3","biotype":"lincRNA","ncbi_id":"140849","summary":null,"start":64290385,"end":64313132,"strand":1,"description":"long intergenic non-protein coding RNA 266-1 [Source:HGNC Symbol;Acc:HGNC:16202]"}, {"versioned_ensembl_gene_id":"ENSG00000171132.13","gene_symbol":"PRKCE","gene_name":"protein kinase C epsilon [Source:HGNC Symbol;Acc:HGNC:9401]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5581","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This kinase has been shown to be involved in many different cellular functions, such as neuron channel activation, apoptosis, cardioprotection from ischemia, heat shock response, as well as insulin exocytosis. Knockout studies in mice suggest that this kinase is important for lipopolysaccharide (LPS)-mediated signaling in activated macrophages and may also play a role in controlling anxiety-like behavior. [provided by RefSeq, Jul 2008]","start":45651345,"end":46187990,"strand":1,"description":"protein kinase C epsilon [Source:HGNC Symbol;Acc:HGNC:9401]"}, {"versioned_ensembl_gene_id":"ENSG00000165985.9","gene_symbol":"C1QL3","gene_name":"complement C1q like 3 [Source:HGNC Symbol;Acc:HGNC:19359]","synonyms":"K100,CTRP13,C1QTNF13,C1ql","biotype":"protein_coding","ncbi_id":"389941","summary":null,"start":16513743,"end":16522005,"strand":-1,"description":"complement C1q like 3 [Source:HGNC Symbol;Acc:HGNC:19359]"}, {"versioned_ensembl_gene_id":"ENSG00000268847.1","gene_symbol":"SIGLEC31P","gene_name":"sialic acid binding Ig like lectin 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:16072]","synonyms":"SIGLECP15","biotype":"unprocessed_pseudogene","ncbi_id":"114189","summary":null,"start":56589495,"end":56590281,"strand":-1,"description":"sialic acid binding Ig like lectin 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:16072]"}, {"versioned_ensembl_gene_id":"ENSG00000224560.3","gene_symbol":"AC108043.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45414337,"end":45414910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251414.1","gene_symbol":"AC138956.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176354206,"end":176356168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124067.16","gene_symbol":"SLC12A4","gene_name":"solute carrier family 12 member 4 [Source:HGNC Symbol;Acc:HGNC:10913]","synonyms":"KCC1","biotype":"protein_coding","ncbi_id":"6560","summary":"This gene encodes a member of the SLC12A transporter family. The encoded protein mediates the coupled movement of potassium and chloride ions across the plasma membrane. This gene is expressed ubiquitously. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2013]","start":67943474,"end":67969601,"strand":-1,"description":"solute carrier family 12 member 4 [Source:HGNC Symbol;Acc:HGNC:10913]"}, {"versioned_ensembl_gene_id":"ENSG00000229685.8","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33042507,"end":33058713,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000236443.6","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32994477,"end":32998463,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000163539.16","gene_symbol":"CLASP2","gene_name":"cytoplasmic linker associated protein 2 [Source:HGNC Symbol;Acc:HGNC:17078]","synonyms":"KIAA0627","biotype":"protein_coding","ncbi_id":"23122","summary":null,"start":33496245,"end":33718356,"strand":-1,"description":"cytoplasmic linker associated protein 2 [Source:HGNC Symbol;Acc:HGNC:17078]"}, {"versioned_ensembl_gene_id":"ENSG00000240045.1","gene_symbol":"DWORF","gene_name":"DWARF open reading frame [Source:NCBI gene;Acc:100507537]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507537","summary":null,"start":155290229,"end":155293775,"strand":-1,"description":"DWARF open reading frame [Source:NCBI gene;Acc:100507537]"}, {"versioned_ensembl_gene_id":"ENSG00000227621.1","gene_symbol":"PHBP11","gene_name":"prohibitin pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644214","summary":null,"start":223856579,"end":223857387,"strand":-1,"description":"prohibitin pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39290]"}, {"versioned_ensembl_gene_id":"ENSG00000259262.1","gene_symbol":"NDUFA3P4","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45053]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480806","summary":null,"start":90385814,"end":90386063,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45053]"}, {"versioned_ensembl_gene_id":"ENSG00000244337.2","gene_symbol":"AJ239322.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131958277,"end":131965535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264791.1","gene_symbol":"AC004147.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34142947,"end":34147047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253219.1","gene_symbol":"KRT18P41","gene_name":"keratin 18 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:33411]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"345430","summary":null,"start":170140664,"end":170141940,"strand":-1,"description":"keratin 18 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:33411]"}, {"versioned_ensembl_gene_id":"ENSG00000266535.1","gene_symbol":"AC008133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33111858,"end":33131743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214484.3","gene_symbol":"RPSAP28","gene_name":"ribosomal protein SA pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391387","summary":null,"start":73370019,"end":73370892,"strand":1,"description":"ribosomal protein SA pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35612]"}, {"versioned_ensembl_gene_id":"ENSG00000249942.1","gene_symbol":"AC239584.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74552584,"end":74589481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161610.1","gene_symbol":"HCRT","gene_name":"hypocretin neuropeptide precursor [Source:HGNC Symbol;Acc:HGNC:4847]","synonyms":"PPOX,OX","biotype":"protein_coding","ncbi_id":"3060","summary":"This gene encodes a hypothalamic neuropeptide precursor protein that gives rise to two mature neuropeptides, orexin A and orexin B, by proteolytic processing. Orexin A and orexin B, which bind to orphan G-protein coupled receptors HCRTR1 and HCRTR2, function in the regulation of sleep and arousal. This neuropeptide arrangement may also play a role in feeding behavior, metabolism, and homeostasis. [provided by RefSeq, Jan 2010]","start":42184060,"end":42185452,"strand":-1,"description":"hypocretin neuropeptide precursor [Source:HGNC Symbol;Acc:HGNC:4847]"}, {"versioned_ensembl_gene_id":"ENSG00000238171.1","gene_symbol":"AC068196.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181076051,"end":181105968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166377.19","gene_symbol":"ATP9B","gene_name":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]","synonyms":"ATPIIB","biotype":"protein_coding","ncbi_id":"374868","summary":null,"start":79069285,"end":79378283,"strand":1,"description":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]"}, {"versioned_ensembl_gene_id":"ENSG00000170085.17","gene_symbol":"SIMC1","gene_name":"SUMO interacting motifs containing 1 [Source:HGNC Symbol;Acc:HGNC:24779]","synonyms":"PLEIAD,OOMA1,FLJ44216,C5orf25","biotype":"protein_coding","ncbi_id":"375484","summary":null,"start":176238367,"end":176345991,"strand":1,"description":"SUMO interacting motifs containing 1 [Source:HGNC Symbol;Acc:HGNC:24779]"}, {"versioned_ensembl_gene_id":"ENSG00000265671.1","gene_symbol":"AP000894.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":894435,"end":907680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249485.1","gene_symbol":"RBBP4P1","gene_name":"RB binding protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42368]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642954","summary":null,"start":14797125,"end":14798400,"strand":-1,"description":"RB binding protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42368]"}, {"versioned_ensembl_gene_id":"ENSG00000224466.1","gene_symbol":"CDCA4P2","gene_name":"cell division cycle associated 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49771]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129348","summary":null,"start":86552625,"end":86553342,"strand":-1,"description":"cell division cycle associated 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49771]"}, {"versioned_ensembl_gene_id":"ENSG00000253656.1","gene_symbol":"AC090987.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130595299,"end":130655712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280734.2","gene_symbol":"LINC01232","gene_name":"long intergenic non-protein coding RNA 1232 [Source:HGNC Symbol;Acc:HGNC:49755]","synonyms":"TCONS_00021520,FLJ41590","biotype":"processed_transcript","ncbi_id":"102725509","summary":null,"start":99486962,"end":99499306,"strand":-1,"description":"long intergenic non-protein coding RNA 1232 [Source:HGNC Symbol;Acc:HGNC:49755]"}, {"versioned_ensembl_gene_id":"ENSG00000186635.14","gene_symbol":"ARAP1","gene_name":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:16925]","synonyms":"CENTD2","biotype":"protein_coding","ncbi_id":"116985","summary":"The protein encoded by this gene contains SAM, ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology (PH) domains. In vitro, this protein displays RHO-GAP and phosphatidylinositol (3,4,5) trisphosphate (PIP3)-dependent ARF-GAP activity. The encoded protein associates with the Golgi, and the ARF-GAP activity mediates changes in the Golgi and the formation of filopodia. It is thought to regulate the cell-specific trafficking of a receptor protein involved in apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":72685069,"end":72793599,"strand":-1,"description":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:HGNC:16925]"}, {"versioned_ensembl_gene_id":"ENSG00000188883.4","gene_symbol":"KLRG2","gene_name":"killer cell lectin like receptor G2 [Source:HGNC Symbol;Acc:HGNC:24778]","synonyms":"FLJ44186,CLEC15B","biotype":"protein_coding","ncbi_id":"346689","summary":null,"start":139452690,"end":139483712,"strand":-1,"description":"killer cell lectin like receptor G2 [Source:HGNC Symbol;Acc:HGNC:24778]"}, {"versioned_ensembl_gene_id":"ENSG00000198157.10","gene_symbol":"HMGN5","gene_name":"high mobility group nucleosome binding domain 5 [Source:HGNC Symbol;Acc:HGNC:8013]","synonyms":"NSBP1","biotype":"protein_coding","ncbi_id":"79366","summary":"This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009]","start":81113701,"end":81201942,"strand":-1,"description":"high mobility group nucleosome binding domain 5 [Source:HGNC Symbol;Acc:HGNC:8013]"}, {"versioned_ensembl_gene_id":"ENSG00000228328.2","gene_symbol":"AL158201.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68070520,"end":68071767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278131.1","gene_symbol":"AC116050.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91589494,"end":91621421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236988.2","gene_symbol":"AL359641.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100149783,"end":100151340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247700.4","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29879004,"end":29881726,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000275490.1","gene_symbol":"AC233263.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90309230,"end":90309333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223530.1","gene_symbol":"AC012506.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23330664,"end":23332044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238241.1","gene_symbol":"CCR12P","gene_name":"C-C motif chemokine receptor 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:39812]","synonyms":"GPR183P1","biotype":"processed_pseudogene","ncbi_id":"100133168","summary":null,"start":99407781,"end":99409062,"strand":-1,"description":"C-C motif chemokine receptor 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:39812]"}, {"versioned_ensembl_gene_id":"ENSG00000282794.1","gene_symbol":"IGHV3-57","gene_name":"immunoglobulin heavy variable 3-57 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5612]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28418","summary":null,"start":106643575,"end":106643854,"strand":-1,"description":"immunoglobulin heavy variable 3-57 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5612]"}, {"versioned_ensembl_gene_id":"ENSG00000283511.1","gene_symbol":"AC137936.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":58180009,"end":58187495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283148.1","gene_symbol":"AC137936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58174478,"end":58178374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197858.10","gene_symbol":"GPAA1","gene_name":"glycosylphosphatidylinositol anchor attachment 1 [Source:HGNC Symbol;Acc:HGNC:4446]","synonyms":"hGAA1,GAA1","biotype":"protein_coding","ncbi_id":"8733","summary":"Posttranslational glycosylphosphatidylinositol (GPI) anchor attachment serves as a general mechanism for linking proteins to the cell surface membrane. The protein encoded by this gene presumably functions in GPI anchoring at the GPI transfer step. The mRNA transcript is ubiquitously expressed in both fetal and adult tissues. The anchor attachment protein 1 contains an N-terminal signal sequence, 1 cAMP- and cGMP-dependent protein kinase phosphorylation site, 1 leucine zipper pattern, 2 potential N-glycosylation sites, and 8 putative transmembrane domains. [provided by RefSeq, Jul 2008]","start":144082590,"end":144086216,"strand":1,"description":"glycosylphosphatidylinositol anchor attachment 1 [Source:HGNC Symbol;Acc:HGNC:4446]"}, {"versioned_ensembl_gene_id":"ENSG00000230600.1","gene_symbol":"AC073188.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63380466,"end":63385789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100104.13","gene_symbol":"SRRD","gene_name":"SRR1 domain containing [Source:HGNC Symbol;Acc:HGNC:33910]","synonyms":"SRR1L,HC/HCC","biotype":"protein_coding","ncbi_id":"402055","summary":null,"start":26483877,"end":26494658,"strand":1,"description":"SRR1 domain containing [Source:HGNC Symbol;Acc:HGNC:33910]"}, {"versioned_ensembl_gene_id":"ENSG00000007376.7","gene_symbol":"RPUSD1","gene_name":"RNA pseudouridylate synthase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14173]","synonyms":"RLUCL,MGC19600,C16orf40","biotype":"protein_coding","ncbi_id":"113000","summary":null,"start":784974,"end":788397,"strand":-1,"description":"RNA pseudouridylate synthase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14173]"}, {"versioned_ensembl_gene_id":"ENSG00000185905.3","gene_symbol":"C16orf54","gene_name":"chromosome 16 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26649]","synonyms":"FLJ35681","biotype":"protein_coding","ncbi_id":"283897","summary":null,"start":29742463,"end":29746006,"strand":-1,"description":"chromosome 16 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:26649]"}, {"versioned_ensembl_gene_id":"ENSG00000174521.7","gene_symbol":"TTC9B","gene_name":"tetratricopeptide repeat domain 9B [Source:HGNC Symbol;Acc:HGNC:26395]","synonyms":"FLJ30373","biotype":"protein_coding","ncbi_id":"148014","summary":null,"start":40216058,"end":40218399,"strand":-1,"description":"tetratricopeptide repeat domain 9B [Source:HGNC Symbol;Acc:HGNC:26395]"}, {"versioned_ensembl_gene_id":"ENSG00000229372.1","gene_symbol":"SZT2-AS1","gene_name":"SZT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41225]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873952","summary":null,"start":43447776,"end":43448644,"strand":-1,"description":"SZT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41225]"}, {"versioned_ensembl_gene_id":"ENSG00000213244.3","gene_symbol":"HIST2H3DP1","gene_name":"histone cluster 2 H3 family member d pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43797]","synonyms":"p05","biotype":"unprocessed_pseudogene","ncbi_id":"106479023","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a transcribed histone pseudogene found on chromosome 1. [provided by RefSeq, Mar 2019]","start":121118195,"end":121118610,"strand":-1,"description":"histone cluster 2 H3 family member d pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43797]"}, {"versioned_ensembl_gene_id":"ENSG00000275938.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39","biotype":"unprocessed_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832765,"end":54848078,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000127951.6","gene_symbol":"FGL2","gene_name":"fibrinogen like 2 [Source:HGNC Symbol;Acc:HGNC:3696]","synonyms":"T49,pT49","biotype":"protein_coding","ncbi_id":"10875","summary":"The protein encoded by this gene is a secreted protein that is similar to the beta- and gamma-chains of fibrinogen. The carboxyl-terminus of the encoded protein consists of the fibrinogen-related domains (FRED). The encoded protein forms a tetrameric complex which is stabilized by interchain disulfide bonds. This protein may play a role in physiologic functions at mucosal sites. [provided by RefSeq, Jul 2008]","start":77193371,"end":77199848,"strand":-1,"description":"fibrinogen like 2 [Source:HGNC Symbol;Acc:HGNC:3696]"}, {"versioned_ensembl_gene_id":"ENSG00000268993.1","gene_symbol":"AC244453.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121142051,"end":121142438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275288.6","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816438,"end":54830737,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000165694.9","gene_symbol":"FRMD7","gene_name":"FERM domain containing 7 [Source:HGNC Symbol;Acc:HGNC:8079]","synonyms":"NYS1,NYS,FLJ43346","biotype":"protein_coding","ncbi_id":"90167","summary":"Mutations in this gene are associated with X-linked congenital nystagmus. [provided by RefSeq, Dec 2008]","start":132076993,"end":132128020,"strand":-1,"description":"FERM domain containing 7 [Source:HGNC Symbol;Acc:HGNC:8079]"}, {"versioned_ensembl_gene_id":"ENSG00000227193.2","gene_symbol":"AC244453.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121118126,"end":121146826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116151.13","gene_symbol":"MORN1","gene_name":"MORN repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:25852]","synonyms":"FLJ13941","biotype":"protein_coding","ncbi_id":"79906","summary":null,"start":2321253,"end":2391707,"strand":-1,"description":"MORN repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:25852]"}, {"versioned_ensembl_gene_id":"ENSG00000174992.7","gene_symbol":"ZG16","gene_name":"zymogen granule protein 16 [Source:HGNC Symbol;Acc:HGNC:30961]","synonyms":"ZG16A,JCLN1,JCLN,hZG16","biotype":"protein_coding","ncbi_id":"653808","summary":null,"start":29778240,"end":29782973,"strand":1,"description":"zymogen granule protein 16 [Source:HGNC Symbol;Acc:HGNC:30961]"}, {"versioned_ensembl_gene_id":"ENSG00000229301.1","gene_symbol":"AC006455.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63354457,"end":63359306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197798.8","gene_symbol":"FAM118B","gene_name":"family with sequence similarity 118 member B [Source:HGNC Symbol;Acc:HGNC:26110]","synonyms":"FLJ21103","biotype":"protein_coding","ncbi_id":"79607","summary":null,"start":126211414,"end":126262986,"strand":1,"description":"family with sequence similarity 118 member B [Source:HGNC Symbol;Acc:HGNC:26110]"}, {"versioned_ensembl_gene_id":"ENSG00000231087.2","gene_symbol":"FDPSP7","gene_name":"farnesyl diphosphate synthase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33487]","synonyms":"FDPSL2B","biotype":"processed_pseudogene","ncbi_id":"441261","summary":null,"start":76968197,"end":76969250,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33487]"}, {"versioned_ensembl_gene_id":"ENSG00000141316.12","gene_symbol":"SPACA3","gene_name":"sperm acrosome associated 3 [Source:HGNC Symbol;Acc:HGNC:16260]","synonyms":"LYC3,CT54,ALLP17,SLLP1,LYZL3","biotype":"protein_coding","ncbi_id":"124912","summary":"The protein encoded by this gene is a sperm surface protein that may be involved in adhesion to the egg prior to fertilization. While the encoded protein has significant similarity to lysozyme at the amino acid level, it has no detectable bacteriocidal activity. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":32970376,"end":32997877,"strand":1,"description":"sperm acrosome associated 3 [Source:HGNC Symbol;Acc:HGNC:16260]"}, {"versioned_ensembl_gene_id":"ENSG00000236280.1","gene_symbol":"AC114737.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76968346,"end":76968518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205482.9","gene_symbol":"SPDYE18","gene_name":"speedy/RINGO cell cycle regulator family member E18 [Source:HGNC Symbol;Acc:HGNC:51514]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100505767","summary":null,"start":77052785,"end":77060512,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E18 [Source:HGNC Symbol;Acc:HGNC:51514]"}, {"versioned_ensembl_gene_id":"ENSG00000066654.13","gene_symbol":"THUMPD1","gene_name":"THUMP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23807]","synonyms":"Tan1,FLJ20274","biotype":"protein_coding","ncbi_id":"55623","summary":null,"start":20702816,"end":20742084,"strand":-1,"description":"THUMP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23807]"}, {"versioned_ensembl_gene_id":"ENSG00000259628.1","gene_symbol":"AC007000.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":77043721,"end":77198626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266955.1","gene_symbol":"AP001269.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11993988,"end":11994938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253868.3","gene_symbol":"FER1L6-AS2","gene_name":"FER1L6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:26534]","synonyms":"FLJ32770,C8orf78","biotype":"antisense_RNA","ncbi_id":"157376","summary":null,"start":124046073,"end":124171522,"strand":-1,"description":"FER1L6 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:26534]"}, {"versioned_ensembl_gene_id":"ENSG00000213204.8","gene_symbol":"AL049697.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":87408012,"end":87511634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265773.1","gene_symbol":"NUP210P2","gene_name":"nucleoporin 210 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42707]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129929","summary":null,"start":11901932,"end":11903166,"strand":1,"description":"nucleoporin 210 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42707]"}, {"versioned_ensembl_gene_id":"ENSG00000251369.8","gene_symbol":"ZNF550","gene_name":"zinc finger protein 550 [Source:HGNC Symbol;Acc:HGNC:28643]","synonyms":"MGC41917","biotype":"protein_coding","ncbi_id":"162972","summary":null,"start":57535257,"end":57559863,"strand":-1,"description":"zinc finger protein 550 [Source:HGNC Symbol;Acc:HGNC:28643]"}, {"versioned_ensembl_gene_id":"ENSG00000232754.1","gene_symbol":"AL035658.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41169190,"end":41183144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229294.1","gene_symbol":"AL139294.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65279456,"end":65306521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255309.1","gene_symbol":"AC131935.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11759101,"end":11759433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229710.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32634806,"end":32635637,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000187244.10","gene_symbol":"BCAM","gene_name":"basal cell adhesion molecule (Lutheran blood group) [Source:HGNC Symbol;Acc:HGNC:6722]","synonyms":"LU,CD239","biotype":"protein_coding","ncbi_id":"4059","summary":"This gene encodes Lutheran blood group glycoprotein, a member of the immunoglobulin superfamily and a receptor for the extracellular matrix protein, laminin. The protein contains five extracellular immunoglobulin domains, a single transmembrane domain, and a short C-terminal cytoplasmic tail. This protein may play a role in epithelial cell cancer and in vaso-occlusion of red blood cells in sickle cell disease. Polymorphisms in this gene define some of the antigens in the Lutheran system and also the Auberger system. Inactivating variants of this gene result in the recessive Lutheran null phenotype, Lu(a-b-), of the Lutheran blood group. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":44809059,"end":44821420,"strand":1,"description":"basal cell adhesion molecule (Lutheran blood group) [Source:HGNC Symbol;Acc:HGNC:6722]"}, {"versioned_ensembl_gene_id":"ENSG00000230590.9","gene_symbol":"FTX","gene_name":"FTX transcript, XIST regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37190]","synonyms":"NCRNA00182,MIR374AHG,LINC00182,FLJ33139","biotype":"lincRNA","ncbi_id":"100302692","summary":"This gene is located upstream of XIST, within the X-inactivation center (XIC). It produces a spliced long non-coding RNA that is thought to positively regulate the expression of XIST, which is essential for the initiation and spread of X-inactivation. [provided by RefSeq, May 2015]","start":73946555,"end":74293574,"strand":-1,"description":"FTX transcript, XIST regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37190]"}, {"versioned_ensembl_gene_id":"ENSG00000132204.13","gene_symbol":"LINC00470","gene_name":"long intergenic non-protein coding RNA 470 [Source:HGNC Symbol;Acc:HGNC:1225]","synonyms":"C18orf2","biotype":"lincRNA","ncbi_id":"56651","summary":null,"start":1254383,"end":1408344,"strand":-1,"description":"long intergenic non-protein coding RNA 470 [Source:HGNC Symbol;Acc:HGNC:1225]"}, {"versioned_ensembl_gene_id":"ENSG00000234144.1","gene_symbol":"COX6CP13","gene_name":"cytochrome c oxidase subunit 6C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49365]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480267","summary":null,"start":65298755,"end":65298980,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49365]"}, {"versioned_ensembl_gene_id":"ENSG00000214657.4","gene_symbol":"AC113608.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15869939,"end":15870243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237326.1","gene_symbol":"AC113608.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15801747,"end":15810877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268486.5","gene_symbol":"FO681491.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18408806,"end":18431605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282089.1","gene_symbol":"IGHD3OR15-3B","gene_name":"immunoglobulin heavy diversity 3/OR15-3B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5501]","synonyms":"IGHD3OR153B,IGHD3/OR15-3B","biotype":"IG_D_gene","ncbi_id":"28330","summary":null,"start":21012559,"end":21012589,"strand":-1,"description":"immunoglobulin heavy diversity 3/OR15-3B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5501]"}, {"versioned_ensembl_gene_id":"ENSG00000177359.18","gene_symbol":"AC024940.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31111652,"end":31206154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278902.1","gene_symbol":"AC010947.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73921939,"end":73922631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249119.1","gene_symbol":"MTND6P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39467]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478943","summary":null,"start":134924123,"end":134924644,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39467]"}, {"versioned_ensembl_gene_id":"ENSG00000261780.2","gene_symbol":"AC105243.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73324941,"end":73349878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184937.13","gene_symbol":"WT1","gene_name":"Wilms tumor 1 [Source:HGNC Symbol;Acc:HGNC:12796]","synonyms":"WIT-2,WAGR,NPHS4,GUD,AWT1","biotype":"protein_coding","ncbi_id":"7490","summary":"This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. Authors of PMID:7926762 also provide evidence that WT1 mRNA undergoes RNA editing in human and rat, and that this process is tissue-restricted and developmentally regulated. [provided by RefSeq, Mar 2015]","start":32387775,"end":32435630,"strand":-1,"description":"Wilms tumor 1 [Source:HGNC Symbol;Acc:HGNC:12796]"}, {"versioned_ensembl_gene_id":"ENSG00000259410.5","gene_symbol":"AC009292.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":67832725,"end":67873866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243276.5","gene_symbol":"AC068633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118004819,"end":118557668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245719.1","gene_symbol":"AC009292.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67834310,"end":67838879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248923.1","gene_symbol":"MTND5P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506169","summary":null,"start":134924648,"end":134926459,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42273]"}, {"versioned_ensembl_gene_id":"ENSG00000198894.7","gene_symbol":"CIPC","gene_name":"CLOCK interacting pacemaker [Source:HGNC Symbol;Acc:HGNC:20365]","synonyms":"KIAA1737","biotype":"protein_coding","ncbi_id":"85457","summary":null,"start":77098097,"end":77117287,"strand":1,"description":"CLOCK interacting pacemaker [Source:HGNC Symbol;Acc:HGNC:20365]"}, {"versioned_ensembl_gene_id":"ENSG00000269883.1","gene_symbol":"AC007375.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77140683,"end":77142996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277245.1","gene_symbol":"AC084782.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56447120,"end":56447697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186056.9","gene_symbol":"MATN1-AS1","gene_name":"MATN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40364]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129196","summary":null,"start":30718504,"end":30726827,"strand":1,"description":"MATN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40364]"}, {"versioned_ensembl_gene_id":"ENSG00000234724.1","gene_symbol":"HDAC1P1","gene_name":"histone deacetylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45190]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419595","summary":null,"start":94137748,"end":94139500,"strand":1,"description":"histone deacetylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45190]"}, {"versioned_ensembl_gene_id":"ENSG00000079691.17","gene_symbol":"CARMIL1","gene_name":"capping protein regulator and myosin 1 linker 1 [Source:HGNC Symbol;Acc:HGNC:21581]","synonyms":"LRRC16A,LRRC16,FLJ20048,dJ501N12.1,CARMIL","biotype":"protein_coding","ncbi_id":"55604","summary":null,"start":25279078,"end":25620530,"strand":1,"description":"capping protein regulator and myosin 1 linker 1 [Source:HGNC Symbol;Acc:HGNC:21581]"}, {"versioned_ensembl_gene_id":"ENSG00000122877.15","gene_symbol":"EGR2","gene_name":"early growth response 2 [Source:HGNC Symbol;Acc:HGNC:3239]","synonyms":"KROX20","biotype":"protein_coding","ncbi_id":"1959","summary":"The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":62811996,"end":62919900,"strand":-1,"description":"early growth response 2 [Source:HGNC Symbol;Acc:HGNC:3239]"}, {"versioned_ensembl_gene_id":"ENSG00000142182.8","gene_symbol":"DNMT3L","gene_name":"DNA methyltransferase 3 like [Source:HGNC Symbol;Acc:HGNC:2980]","synonyms":"MGC1090","biotype":"protein_coding","ncbi_id":"29947","summary":"CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a nuclear protein with similarity to DNA methyltransferases, but is not thought to function as a DNA methyltransferase as it does not contain the amino acid residues necessary for methyltransferase activity. However, it does stimulate de novo methylation by DNA cytosine methyltransferase 3 alpha and is thought to be required for the establishment of maternal genomic imprints. This protein also mediates transcriptional repression through interaction with histone deacetylase 1. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]","start":44246339,"end":44262216,"strand":-1,"description":"DNA methyltransferase 3 like [Source:HGNC Symbol;Acc:HGNC:2980]"}, {"versioned_ensembl_gene_id":"ENSG00000175485.2","gene_symbol":"OR52W1","gene_name":"olfactory receptor family 52 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:15239]","synonyms":"OR52W1P","biotype":"protein_coding","ncbi_id":"120787","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6199146,"end":6200259,"strand":1,"description":"olfactory receptor family 52 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:15239]"}, {"versioned_ensembl_gene_id":"ENSG00000179571.10","gene_symbol":"NBPF17P","gene_name":"NBPF member 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:31997]","synonyms":"NBPF23P,NBPF23","biotype":"unprocessed_pseudogene","ncbi_id":"401967","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2014]","start":143595216,"end":143635641,"strand":-1,"description":"NBPF member 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:31997]"}, {"versioned_ensembl_gene_id":"ENSG00000261959.1","gene_symbol":"AC015909.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50163523,"end":50165316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156482.10","gene_symbol":"RPL30","gene_name":"ribosomal protein L30 [Source:HGNC Symbol;Acc:HGNC:10333]","synonyms":"L30","biotype":"protein_coding","ncbi_id":"6156","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L30E family of ribosomal proteins. It is located in the cytoplasm. This gene is co-transcribed with the U72 small nucleolar RNA gene, which is located in its fourth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":98024851,"end":98046469,"strand":-1,"description":"ribosomal protein L30 [Source:HGNC Symbol;Acc:HGNC:10333]"}, {"versioned_ensembl_gene_id":"ENSG00000236047.1","gene_symbol":"AC073410.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202520401,"end":202520989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240393.1","gene_symbol":"AC092691.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117674342,"end":117675144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270868.1","gene_symbol":"AP000942.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102306112,"end":102306271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243777.1","gene_symbol":"AP000942.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102295060,"end":102295806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179447.2","gene_symbol":"AL049647.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19242302,"end":19284596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229807.10","gene_symbol":"XIST","gene_name":"X inactive specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:12810]","synonyms":"swd66,NCRNA00001,LINC00001,DXS399E,DXS1089","biotype":"lincRNA","ncbi_id":"7503","summary":"X inactivation is an early developmental process in mammalian females that transcriptionally silences one of the pair of X chromosomes, thus providing dosage equivalence between males and females. The process is regulated by several factors, including a region of chromosome X called the X inactivation center (XIC). The XIC comprises several non-coding and protein-coding genes, and this gene was the first non-coding gene identified within the XIC. This gene is expressed exclusively from the XIC of the inactive X chromosome, and is essential for the initiation and spread of X-inactivation. The transcript is a spliced RNA. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined. Mutations in the XIST promoter cause familial skewed X inactivation. [provided by RefSeq, Apr 2012]","start":73820651,"end":73852753,"strand":-1,"description":"X inactive specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:12810]"}, {"versioned_ensembl_gene_id":"ENSG00000229349.2","gene_symbol":"ACTG1P9","gene_name":"actin gamma 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:154]","synonyms":"ACTGP9","biotype":"processed_pseudogene","ncbi_id":"82","summary":null,"start":46204729,"end":46207386,"strand":1,"description":"actin gamma 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:154]"}, {"versioned_ensembl_gene_id":"ENSG00000258653.3","gene_symbol":"AC005520.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":73851971,"end":73932278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224714.2","gene_symbol":"AC024600.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64901136,"end":64924518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232577.1","gene_symbol":"BX679671.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31992630,"end":31996175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236335.1","gene_symbol":"AL161638.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30409560,"end":30411638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171798.17","gene_symbol":"KNDC1","gene_name":"kinase non-catalytic C-lobe domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29374]","synonyms":"FLJ25027,C10orf23,bB439H18.3,Very-KIND,v-KIND,RASGEF2,KIAA1768","biotype":"protein_coding","ncbi_id":"85442","summary":"The protein encoded by this gene is a Ras guanine nucleotide exchange factor that appears to negatively regulate dendritic growth in the brain. Knockdown of this gene in senescent umbilical vein endothelial cells partially reversed the senescence, showing that this gene could potentially be targeted by anti-aging therapies. [provided by RefSeq, Dec 2016]","start":133160447,"end":133226412,"strand":1,"description":"kinase non-catalytic C-lobe domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29374]"}, {"versioned_ensembl_gene_id":"ENSG00000171942.4","gene_symbol":"OR10H2","gene_name":"olfactory receptor family 10 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8173]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26538","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15728020,"end":15729060,"strand":1,"description":"olfactory receptor family 10 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8173]"}, {"versioned_ensembl_gene_id":"ENSG00000270140.1","gene_symbol":"AC005520.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73905267,"end":73905636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270892.1","gene_symbol":"AC006077.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134863091,"end":134863433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226212.2","gene_symbol":"TRGV6","gene_name":"T-cell receptor gamma variable 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12292]","synonyms":"V1S5P,TCRGV6,TCRGV5P","biotype":"TR_V_pseudogene","ncbi_id":"6980","summary":null,"start":38340700,"end":38340998,"strand":-1,"description":"T-cell receptor gamma variable 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12292]"}, {"versioned_ensembl_gene_id":"ENSG00000237574.1","gene_symbol":"LINC01856","gene_name":"long intergenic non-protein coding RNA 1856 [Source:HGNC Symbol;Acc:HGNC:52672]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927924","summary":null,"start":129923177,"end":129946703,"strand":1,"description":"long intergenic non-protein coding RNA 1856 [Source:HGNC Symbol;Acc:HGNC:52672]"}, {"versioned_ensembl_gene_id":"ENSG00000248455.5","gene_symbol":"LINC02217","gene_name":"long intergenic non-protein coding RNA 2217 [Source:HGNC Symbol;Acc:HGNC:53084]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929544","summary":null,"start":17404019,"end":17441694,"strand":1,"description":"long intergenic non-protein coding RNA 2217 [Source:HGNC Symbol;Acc:HGNC:53084]"}, {"versioned_ensembl_gene_id":"ENSG00000180913.3","gene_symbol":"OR56B3P","gene_name":"olfactory receptor family 56 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401675","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6128610,"end":6129556,"strand":1,"description":"olfactory receptor family 56 subfamily B member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15247]"}, {"versioned_ensembl_gene_id":"ENSG00000233158.1","gene_symbol":"RPS24P6","gene_name":"ribosomal protein S24 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36240]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100216339","summary":null,"start":94912432,"end":94912831,"strand":1,"description":"ribosomal protein S24 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36240]"}, {"versioned_ensembl_gene_id":"ENSG00000236017.8","gene_symbol":"ASMTL-AS1","gene_name":"ASMTL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25811]","synonyms":"NCRNA00105,FLJ13330,CXYorf2,ASMTLAS,ASMTL-AS","biotype":"antisense_RNA","ncbi_id":"80161","summary":"This gene serves as the antisense to the acetylserotonin O-methyltransferase-like gene. Multiple non-coding transcript variants have been found for this gene. [provided by RefSeq, Oct 2011]","start":1401769,"end":1414028,"strand":1,"description":"ASMTL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25811]"}, {"versioned_ensembl_gene_id":"ENSG00000230654.1","gene_symbol":"MTCO2P25","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52154]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075290","summary":null,"start":69330698,"end":69331378,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52154]"}, {"versioned_ensembl_gene_id":"ENSG00000157766.15","gene_symbol":"ACAN","gene_name":"aggrecan [Source:HGNC Symbol;Acc:HGNC:319]","synonyms":"MSK16,CSPGCP,CSPG1,AGC1","biotype":"protein_coding","ncbi_id":"176","summary":"This gene is a member of the aggrecan/versican proteoglycan family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage. Mutations in this gene may be involved in skeletal dysplasia and spinal degeneration. Multiple alternatively spliced transcript variants that encode different protein isoforms have been observed in this gene. [provided by RefSeq, Jul 2008]","start":88803443,"end":88875354,"strand":1,"description":"aggrecan [Source:HGNC Symbol;Acc:HGNC:319]"}, {"versioned_ensembl_gene_id":"ENSG00000284694.1","gene_symbol":"AL355602.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4479131,"end":4484375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233304.6","gene_symbol":"LINC01346","gene_name":"long intergenic non-protein coding RNA 1346 [Source:HGNC Symbol;Acc:HGNC:50563]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728716","summary":null,"start":3940565,"end":3955262,"strand":1,"description":"long intergenic non-protein coding RNA 1346 [Source:HGNC Symbol;Acc:HGNC:50563]"}, {"versioned_ensembl_gene_id":"ENSG00000138796.16","gene_symbol":"HADH","gene_name":"hydroxyacyl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4799]","synonyms":"SCHAD,HADHSC,HADH1","biotype":"protein_coding","ncbi_id":"3033","summary":"This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15. [provided by RefSeq, May 2010]","start":107989714,"end":108035175,"strand":1,"description":"hydroxyacyl-CoA dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4799]"}, {"versioned_ensembl_gene_id":"ENSG00000228675.1","gene_symbol":"AC006482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17679549,"end":17680659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232735.2","gene_symbol":"ATG4AP1","gene_name":"autophagy related 4A cysteine peptidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480786","summary":null,"start":82998699,"end":82999236,"strand":1,"description":"autophagy related 4A cysteine peptidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44081]"}, {"versioned_ensembl_gene_id":"ENSG00000198028.3","gene_symbol":"ZNF560","gene_name":"zinc finger protein 560 [Source:HGNC Symbol;Acc:HGNC:26484]","synonyms":"FLJ31986","biotype":"protein_coding","ncbi_id":"147741","summary":null,"start":9466507,"end":9498607,"strand":-1,"description":"zinc finger protein 560 [Source:HGNC Symbol;Acc:HGNC:26484]"}, {"versioned_ensembl_gene_id":"ENSG00000223361.5","gene_symbol":"FTH1P10","gene_name":"ferritin heavy chain 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3980]","synonyms":"FTHL10","biotype":"transcribed_processed_pseudogene","ncbi_id":"2502","summary":null,"start":17353695,"end":17354624,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:3980]"}, {"versioned_ensembl_gene_id":"ENSG00000116667.12","gene_symbol":"C1orf21","gene_name":"chromosome 1 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:15494]","synonyms":"PIG13","biotype":"protein_coding","ncbi_id":"81563","summary":null,"start":184387058,"end":184629020,"strand":1,"description":"chromosome 1 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:15494]"}, {"versioned_ensembl_gene_id":"ENSG00000171489.10","gene_symbol":"SPACA5","gene_name":"sperm acrosome associated 5 [Source:HGNC Symbol;Acc:HGNC:31353]","synonyms":"UNQ6288,SLLP2,PNPK6288,LYZL5,LYC5,dJ54B20.3","biotype":"protein_coding","ncbi_id":"389852","summary":null,"start":48004336,"end":48009729,"strand":1,"description":"sperm acrosome associated 5 [Source:HGNC Symbol;Acc:HGNC:31353]"}, {"versioned_ensembl_gene_id":"ENSG00000277697.1","gene_symbol":"AL591441.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42978851,"end":42979918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198912.10","gene_symbol":"C1orf174","gene_name":"chromosome 1 open reading frame 174 [Source:HGNC Symbol;Acc:HGNC:27915]","synonyms":"RP13-531C17.2","biotype":"protein_coding","ncbi_id":"339448","summary":null,"start":3889125,"end":3900293,"strand":-1,"description":"chromosome 1 open reading frame 174 [Source:HGNC Symbol;Acc:HGNC:27915]"}, {"versioned_ensembl_gene_id":"ENSG00000265069.1","gene_symbol":"AP002409.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6954677,"end":6957419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268651.2","gene_symbol":"CTAG1A","gene_name":"cancer/testis antigen 1A [Source:HGNC Symbol;Acc:HGNC:24198]","synonyms":"LAGE2A,ESO1","biotype":"protein_coding","ncbi_id":"246100","summary":"The protein encoded by this gene is a tumor cell antigen found in various types of cancers, which makes it a good candidate for a cancer vaccine. This gene is also highly expressed in normal ovary and testis tissues. An identical copy of this gene is found on the same chromosome. [provided by RefSeq, Dec 2015]","start":154585143,"end":154586821,"strand":1,"description":"cancer/testis antigen 1A [Source:HGNC Symbol;Acc:HGNC:24198]"}, {"versioned_ensembl_gene_id":"ENSG00000188580.14","gene_symbol":"NKAIN2","gene_name":"sodium/potassium transporting ATPase interacting 2 [Source:HGNC Symbol;Acc:HGNC:16443]","synonyms":"TCBA1,FAM77B","biotype":"protein_coding","ncbi_id":"154215","summary":"This gene encodes a transmembrane protein that interacts with the beta subunit of a sodium/potassium-transporting ATPase. A chromosomal translocation involving this gene is a cause of lymphoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":123804141,"end":124825657,"strand":1,"description":"sodium/potassium transporting ATPase interacting 2 [Source:HGNC Symbol;Acc:HGNC:16443]"}, {"versioned_ensembl_gene_id":"ENSG00000255928.1","gene_symbol":"AP002993.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73722349,"end":73722694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259529.1","gene_symbol":"AL136295.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24151218,"end":24167402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107862.4","gene_symbol":"GBF1","gene_name":"golgi brefeldin A resistant guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:4181]","synonyms":"KIAA0248,ARF1GEF","biotype":"protein_coding","ncbi_id":"8729","summary":"This gene encodes a member of the Sec7 domain family. The encoded protein is a guanine nucleotide exchange factor that regulates the recruitment of proteins to membranes by mediating GDP to GTP exchange. The encoded protein is localized to the Golgi apparatus and plays a role in vesicular trafficking by activating ADP ribosylation factor 1. The encoded protein has also been identified as an important host factor for viral replication. Multiple transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]","start":102245532,"end":102382899,"strand":1,"description":"golgi brefeldin A resistant guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:4181]"}, {"versioned_ensembl_gene_id":"ENSG00000162415.6","gene_symbol":"ZSWIM5","gene_name":"zinc finger SWIM-type containing 5 [Source:HGNC Symbol;Acc:HGNC:29299]","synonyms":"KIAA1511","biotype":"protein_coding","ncbi_id":"57643","summary":null,"start":45016399,"end":45306209,"strand":-1,"description":"zinc finger SWIM-type containing 5 [Source:HGNC Symbol;Acc:HGNC:29299]"}, {"versioned_ensembl_gene_id":"ENSG00000205086.6","gene_symbol":"C2orf91","gene_name":"chromosome 2 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:42966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400950","summary":null,"start":41935368,"end":41954266,"strand":-1,"description":"chromosome 2 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:42966]"}, {"versioned_ensembl_gene_id":"ENSG00000132631.5","gene_symbol":"SCP2D1","gene_name":"SCP2 sterol binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16211]","synonyms":"HSD22,dJ1068E13.2,C20orf79","biotype":"protein_coding","ncbi_id":"140856","summary":null,"start":18813726,"end":18814392,"strand":1,"description":"SCP2 sterol binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16211]"}, {"versioned_ensembl_gene_id":"ENSG00000232502.1","gene_symbol":"AC073464.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94760774,"end":94761116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223564.1","gene_symbol":"CYP4F32P","gene_name":"cytochrome P450 family 4 subfamily F member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:39951]","synonyms":"CYP4F-se5[6:8]","biotype":"unprocessed_pseudogene","ncbi_id":"107133497","summary":null,"start":94759259,"end":94760279,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:39951]"}, {"versioned_ensembl_gene_id":"ENSG00000217044.1","gene_symbol":"MTCO3P31","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075186","summary":null,"start":153667318,"end":153668106,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52134]"}, {"versioned_ensembl_gene_id":"ENSG00000100987.14","gene_symbol":"VSX1","gene_name":"visual system homeobox 1 [Source:HGNC Symbol;Acc:HGNC:12723]","synonyms":"PPD,PPCD1,PPCD","biotype":"protein_coding","ncbi_id":"30813","summary":"The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":25070885,"end":25082365,"strand":-1,"description":"visual system homeobox 1 [Source:HGNC Symbol;Acc:HGNC:12723]"}, {"versioned_ensembl_gene_id":"ENSG00000251005.1","gene_symbol":"AC105758.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126106139,"end":126106923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205639.10","gene_symbol":"MFSD2B","gene_name":"major facilitator superfamily domain containing 2B [Source:HGNC Symbol;Acc:HGNC:37207]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388931","summary":null,"start":24010081,"end":24063321,"strand":1,"description":"major facilitator superfamily domain containing 2B [Source:HGNC Symbol;Acc:HGNC:37207]"}, {"versioned_ensembl_gene_id":"ENSG00000275743.1","gene_symbol":"AC244472.2","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142587868,"end":142588359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253954.3","gene_symbol":"HMGN1P38","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39422]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643790","summary":null,"start":92711808,"end":92712110,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39422]"}, {"versioned_ensembl_gene_id":"ENSG00000238003.1","gene_symbol":"RPL10P4","gene_name":"ribosomal protein L10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391151","summary":null,"start":201978642,"end":201978949,"strand":1,"description":"ribosomal protein L10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52342]"}, {"versioned_ensembl_gene_id":"ENSG00000240484.1","gene_symbol":"AC091544.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92719393,"end":92719740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273900.1","gene_symbol":"CR848007.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42921443,"end":42921670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268163.1","gene_symbol":"AC004076.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57437970,"end":57477536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271032.1","gene_symbol":"AC020907.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35014961,"end":35025335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271763.1","gene_symbol":"AC091544.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92602910,"end":92620015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229197.1","gene_symbol":"RPS15AP28","gene_name":"ribosomal protein S15a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36381]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132400","summary":null,"start":69300432,"end":69300817,"strand":-1,"description":"ribosomal protein S15a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36381]"}, {"versioned_ensembl_gene_id":"ENSG00000213121.2","gene_symbol":"AL590867.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153231320,"end":153347488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282570.1","gene_symbol":"AC003042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36635060,"end":36635689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258647.5","gene_symbol":"LINC00930","gene_name":"long intergenic non-protein coding RNA 930 [Source:HGNC Symbol;Acc:HGNC:48620]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100144604","summary":null,"start":92567818,"end":92572042,"strand":-1,"description":"long intergenic non-protein coding RNA 930 [Source:HGNC Symbol;Acc:HGNC:48620]"}, {"versioned_ensembl_gene_id":"ENSG00000236533.1","gene_symbol":"AC009413.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41850203,"end":41850601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276597.1","gene_symbol":"AC244196.4","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142554836,"end":142555318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184033.13","gene_symbol":"CTAG1B","gene_name":"cancer/testis antigen 1B [Source:HGNC Symbol;Acc:HGNC:2491]","synonyms":"LAGE2A,ESO1,CTAG1,CTAG,CT6.1,NY-ESO-1,LAGE2B","biotype":"protein_coding","ncbi_id":"1485","summary":"The protein encoded by this gene is an antigen that is overexpressed in many cancers but that is also expressed in normal testis. This gene is found in a duplicated region of the X-chromosome and therefore has a neighboring gene of identical sequence. [provided by RefSeq, Jan 2012]","start":154617609,"end":154619282,"strand":-1,"description":"cancer/testis antigen 1B [Source:HGNC Symbol;Acc:HGNC:2491]"}, {"versioned_ensembl_gene_id":"ENSG00000233465.2","gene_symbol":"BX927141.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800101,"end":29800897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262526.2","gene_symbol":"AC120057.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7240427,"end":7244635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218313.1","gene_symbol":"AL139274.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87173368,"end":87174303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237674.1","gene_symbol":"GSTA7P","gene_name":"glutathione S-transferase alpha 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:4631]","synonyms":"GSTAP6,GSTAP2","biotype":"unprocessed_pseudogene","ncbi_id":"730152","summary":null,"start":52739590,"end":52744656,"strand":-1,"description":"glutathione S-transferase alpha 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:4631]"}, {"versioned_ensembl_gene_id":"ENSG00000272854.1","gene_symbol":"AC004839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107579557,"end":107580057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259007.1","gene_symbol":"AL358333.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51967003,"end":51969800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223816.5","gene_symbol":"IGKV1OR2-2","gene_name":"immunoglobulin kappa variable 1/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49465]","synonyms":"IGKV1/OR2-2","biotype":"unprocessed_pseudogene","ncbi_id":"106481689","summary":null,"start":92034522,"end":92035000,"strand":-1,"description":"immunoglobulin kappa variable 1/OR2-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:49465]"}, {"versioned_ensembl_gene_id":"ENSG00000261779.1","gene_symbol":"AC113208.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75211301,"end":75212167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244756.1","gene_symbol":"AL049874.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60572024,"end":60572311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273493.1","gene_symbol":"AC098479.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58329965,"end":58330118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211727.3","gene_symbol":"TRBV7-6","gene_name":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]","synonyms":"TRBV76,TCRBV7S6,TCRBV6S3A1N1T","biotype":"TR_V_gene","ncbi_id":"28592","summary":null,"start":142492132,"end":142492673,"strand":1,"description":"T-cell receptor beta variable 7-6 [Source:HGNC Symbol;Acc:HGNC:12240]"}, {"versioned_ensembl_gene_id":"ENSG00000214161.3","gene_symbol":"SDC4P","gene_name":"syndecan 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:18903]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"376844","summary":null,"start":30481311,"end":30481911,"strand":-1,"description":"syndecan 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:18903]"}, {"versioned_ensembl_gene_id":"ENSG00000277113.2","gene_symbol":"OR2T3","gene_name":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343173","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248475795,"end":248476751,"strand":1,"description":"olfactory receptor family 2 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:14727]"}, {"versioned_ensembl_gene_id":"ENSG00000237101.1","gene_symbol":"AC092809.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":224219613,"end":224228043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145362.17","gene_symbol":"ANK2","gene_name":"ankyrin 2 [Source:HGNC Symbol;Acc:HGNC:493]","synonyms":"LQT4","biotype":"protein_coding","ncbi_id":"287","summary":"This gene encodes a member of the ankyrin family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton. Ankyrins play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. The protein encoded by this gene is required for targeting and stability of Na/Ca exchanger 1 in cardiomyocytes. Mutations in this gene cause long QT syndrome 4 and cardiac arrhythmia syndrome. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Dec 2011]","start":112818109,"end":113383740,"strand":1,"description":"ankyrin 2 [Source:HGNC Symbol;Acc:HGNC:493]"}, {"versioned_ensembl_gene_id":"ENSG00000226012.1","gene_symbol":"AP001434.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38237217,"end":38238201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249626.1","gene_symbol":"AC024560.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197634315,"end":197635811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255524.7","gene_symbol":"NPIPB8","gene_name":"nuclear pore complex interacting protein family member B8 [Source:HGNC Symbol;Acc:HGNC:37490]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728734","summary":null,"start":28637654,"end":28658682,"strand":1,"description":"nuclear pore complex interacting protein family member B8 [Source:HGNC Symbol;Acc:HGNC:37490]"}, {"versioned_ensembl_gene_id":"ENSG00000198677.10","gene_symbol":"TTC37","gene_name":"tetratricopeptide repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:23639]","synonyms":"THES,KIAA0372","biotype":"protein_coding","ncbi_id":"9652","summary":"This gene encodes a protein with twenty tetratricopeptide (TPR) repeats. Tetratricopeptide repeat containing motifs are found in a variety of proteins and may mediate protein-protein interactions and chaperone activity. Mutations in this gene are associated with trichohepatoenteric syndrome. [provided by RefSeq, Jul 2010]","start":95463895,"end":95555007,"strand":-1,"description":"tetratricopeptide repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:23639]"}, {"versioned_ensembl_gene_id":"ENSG00000172020.12","gene_symbol":"GAP43","gene_name":"growth associated protein 43 [Source:HGNC Symbol;Acc:HGNC:4140]","synonyms":"PP46,B-50","biotype":"protein_coding","ncbi_id":"2596","summary":"The protein encoded by this gene has been termed a 'growth' or 'plasticity' protein because it is expressed at high levels in neuronal growth cones during development and axonal regeneration. This protein is considered a crucial component of an effective regenerative response in the nervous system. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":115623324,"end":115721490,"strand":1,"description":"growth associated protein 43 [Source:HGNC Symbol;Acc:HGNC:4140]"}, {"versioned_ensembl_gene_id":"ENSG00000264315.1","gene_symbol":"HNRNPA1P11","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39129]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128044","summary":null,"start":72618267,"end":72619222,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39129]"}, {"versioned_ensembl_gene_id":"ENSG00000275617.1","gene_symbol":"OR2T4","gene_name":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]","synonyms":"OR2T4Q","biotype":"protein_coding","ncbi_id":"127074","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248361581,"end":248362627,"strand":1,"description":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]"}, {"versioned_ensembl_gene_id":"ENSG00000267871.5","gene_symbol":"AC005261.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57267220,"end":57280334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231830.1","gene_symbol":"AC245140.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154333960,"end":154335037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179632.9","gene_symbol":"MAF1","gene_name":"MAF1 homolog, negative regulator of RNA polymerase III [Source:HGNC Symbol;Acc:HGNC:24966]","synonyms":"DKFZp586G1123","biotype":"protein_coding","ncbi_id":"84232","summary":"This gene encodes a protein that is similar to Maf1, a Saccharomyces cerevisiae protein highly conserved in eukaryotic cells. Yeast Maf1 is a negative effector of RNA polymerase III (Pol III). It responds to changes in the cellular environment and represses pol III transcription. Biochemical studies identified the initiation factor TFIIIB as a target for Maf1-dependent repression. [provided by RefSeq, Jul 2008]","start":144104499,"end":144107611,"strand":1,"description":"MAF1 homolog, negative regulator of RNA polymerase III [Source:HGNC Symbol;Acc:HGNC:24966]"}, {"versioned_ensembl_gene_id":"ENSG00000242278.1","gene_symbol":"AC074051.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5270174,"end":5270954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271858.5","gene_symbol":"CYB561D2","gene_name":"cytochrome b561 family member D2 [Source:NCBI gene;Acc:11068]","synonyms":"TSP10,101F6,XXcos-LUCA11.4,TSP10,101F6","biotype":"antisense_RNA","ncbi_id":"11068","summary":null,"start":50365334,"end":50368197,"strand":1,"description":"cytochrome b561 family member D2 [Source:NCBI gene;Acc:11068]"}, {"versioned_ensembl_gene_id":"ENSG00000275555.2","gene_symbol":"DLL1","gene_name":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"28514","summary":" DLL1 is a human homolog of the Notch Delta ligand and is a member of the delta/serrate/jagged family. It plays a role in mediating cell fate decisions during hematopoiesis. It may play a role in cell-to-cell communication. [provided by RefSeq, Jul 2008]","start":170282206,"end":170306565,"strand":-1,"description":"delta like canonical Notch ligand 1 [Source:HGNC Symbol;Acc:HGNC:2908]"}, {"versioned_ensembl_gene_id":"ENSG00000280000.1","gene_symbol":"AC009135.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6037210,"end":6038977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281761.1","gene_symbol":"AL078605.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170297876,"end":170298375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248946.2","gene_symbol":"MTND3P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52168]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075314","summary":null,"start":49246601,"end":49246915,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:52168]"}, {"versioned_ensembl_gene_id":"ENSG00000250016.2","gene_symbol":"SNX18P23","gene_name":"sorting nexin 18 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132617","summary":null,"start":49233289,"end":49233965,"strand":-1,"description":"sorting nexin 18 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39631]"}, {"versioned_ensembl_gene_id":"ENSG00000100056.11","gene_symbol":"ESS2","gene_name":"ess-2 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:16817]","synonyms":"ES2,DGSI,DGS-H,DGCR14,DGCR13,bis1,ESS-2,Es2el","biotype":"protein_coding","ncbi_id":"8220","summary":"This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":19130279,"end":19144684,"strand":-1,"description":"ess-2 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:16817]"}, {"versioned_ensembl_gene_id":"ENSG00000188321.13","gene_symbol":"ZNF559","gene_name":"zinc finger protein 559 [Source:HGNC Symbol;Acc:HGNC:28197]","synonyms":"MGC13105","biotype":"protein_coding","ncbi_id":"84527","summary":null,"start":9323772,"end":9351162,"strand":1,"description":"zinc finger protein 559 [Source:HGNC Symbol;Acc:HGNC:28197]"}, {"versioned_ensembl_gene_id":"ENSG00000240419.1","gene_symbol":"AC022206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7126293,"end":7126639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231806.2","gene_symbol":"PCAT7","gene_name":"prostate cancer associated transcript 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48824]","synonyms":"PCAN-R2","biotype":"antisense_RNA","ncbi_id":"101928099","summary":null,"start":94555069,"end":94568127,"strand":1,"description":"prostate cancer associated transcript 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48824]"}, {"versioned_ensembl_gene_id":"ENSG00000163516.13","gene_symbol":"ANKZF1","gene_name":"ankyrin repeat and zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25527]","synonyms":"ZNF744,FLJ10415","biotype":"protein_coding","ncbi_id":"55139","summary":null,"start":219229757,"end":219236669,"strand":1,"description":"ankyrin repeat and zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25527]"}, {"versioned_ensembl_gene_id":"ENSG00000203825.4","gene_symbol":"AC239859.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143541768,"end":143572834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188629.11","gene_symbol":"ZNF177","gene_name":"zinc finger protein 177 [Source:HGNC Symbol;Acc:HGNC:12966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7730","summary":null,"start":9363020,"end":9382617,"strand":1,"description":"zinc finger protein 177 [Source:HGNC Symbol;Acc:HGNC:12966]"}, {"versioned_ensembl_gene_id":"ENSG00000263013.1","gene_symbol":"AC133065.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":10938886,"end":10940044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214330.4","gene_symbol":"ABCD1P5","gene_name":"ATP binding cassette subfamily D member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42662]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642762","summary":null,"start":91840601,"end":91843802,"strand":1,"description":"ATP binding cassette subfamily D member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42662]"}, {"versioned_ensembl_gene_id":"ENSG00000259541.5","gene_symbol":"AP001150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120249759,"end":120265932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270293.1","gene_symbol":"AC025588.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57150513,"end":57150978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203647.2","gene_symbol":"AC106827.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66008770,"end":66009200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262211.1","gene_symbol":"AC008914.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55936143,"end":55941727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122390.17","gene_symbol":"NAA60","gene_name":"N(alpha)-acetyltransferase 60, NatF catalytic subunit [Source:HGNC Symbol;Acc:HGNC:25875]","synonyms":"NAT15,FLJ14154","biotype":"protein_coding","ncbi_id":"79903","summary":"This gene encodes an enzyme that localizes to the Golgi apparatus, where it transfers an acetyl group to the N-terminus of free proteins. This enzyme acts on histones, and its activity is important for chromatin assembly and chromosome integrity. Alternative splicing and the use of alternative promoters results in multiple transcript variants. The upstream promoter is located in a differentially methylated region (DMR) and undergoes imprinting; transcript variants originating from this position are expressed from the maternal allele. [provided by RefSeq, Nov 2015]","start":3443611,"end":3486963,"strand":1,"description":"N(alpha)-acetyltransferase 60, NatF catalytic subunit [Source:HGNC Symbol;Acc:HGNC:25875]"}, {"versioned_ensembl_gene_id":"ENSG00000270059.1","gene_symbol":"AC121493.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65359268,"end":65359717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211721.2","gene_symbol":"TRBV6-5","gene_name":"T-cell receptor beta variable 6-5 [Source:HGNC Symbol;Acc:HGNC:12230]","synonyms":"TRBV65,TCRBV6S5,TCRBV13S1","biotype":"TR_V_gene","ncbi_id":"28602","summary":null,"start":142450947,"end":142451448,"strand":1,"description":"T-cell receptor beta variable 6-5 [Source:HGNC Symbol;Acc:HGNC:12230]"}, {"versioned_ensembl_gene_id":"ENSG00000219770.1","gene_symbol":"VN1R11P","gene_name":"vomeronasal 1 receptor 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:13551]","synonyms":"VNR6I2P,hs6V1-2p,dJ86C11.7","biotype":"unitary_pseudogene","ncbi_id":"387317","summary":null,"start":27083280,"end":27084147,"strand":1,"description":"vomeronasal 1 receptor 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:13551]"}, {"versioned_ensembl_gene_id":"ENSG00000230599.2","gene_symbol":"AC018495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10767464,"end":10771718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102104.8","gene_symbol":"RS1","gene_name":"retinoschisin 1 [Source:HGNC Symbol;Acc:HGNC:10457]","synonyms":"XLRS1,RS","biotype":"protein_coding","ncbi_id":"6247","summary":"This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision. [provided by RefSeq, Oct 2008]","start":18639910,"end":18672109,"strand":-1,"description":"retinoschisin 1 [Source:HGNC Symbol;Acc:HGNC:10457]"}, {"versioned_ensembl_gene_id":"ENSG00000223634.1","gene_symbol":"AC012506.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23357516,"end":23360376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241527.1","gene_symbol":"CA15P1","gene_name":"carbonic anhydrase 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44364]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100996435","summary":null,"start":19031564,"end":19034564,"strand":-1,"description":"carbonic anhydrase 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44364]"}, {"versioned_ensembl_gene_id":"ENSG00000274219.1","gene_symbol":"AC025588.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57111120,"end":57112027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261083.1","gene_symbol":"LINC02516","gene_name":"long intergenic non-protein coding RNA 2516 [Source:HGNC Symbol;Acc:HGNC:53505]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927087","summary":null,"start":124499942,"end":124558434,"strand":-1,"description":"long intergenic non-protein coding RNA 2516 [Source:HGNC Symbol;Acc:HGNC:53505]"}, {"versioned_ensembl_gene_id":"ENSG00000228140.1","gene_symbol":"AL031283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15402979,"end":15409433,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138621.11","gene_symbol":"PPCDC","gene_name":"phosphopantothenoylcysteine decarboxylase [Source:HGNC Symbol;Acc:HGNC:28107]","synonyms":"MDS018,FLJ14585","biotype":"protein_coding","ncbi_id":"60490","summary":"Biosynthesis of coenzyme A (CoA) from pantothenic acid (vitamin B5) is an essential universal pathway in prokaryotes and eukaryotes. PPCDC (EC 4.1.1.36), one of the last enzymes in this pathway, converts phosphopantothenoylcysteine to 4-prime-phosphopantetheine (Daugherty et al., 2002 [PubMed 11923312]).[supplied by OMIM, Mar 2008]","start":75023555,"end":75117462,"strand":1,"description":"phosphopantothenoylcysteine decarboxylase [Source:HGNC Symbol;Acc:HGNC:28107]"}, {"versioned_ensembl_gene_id":"ENSG00000277420.1","gene_symbol":"AC245407.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146514471,"end":146525289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153347.9","gene_symbol":"FAM81B","gene_name":"family with sequence similarity 81 member B [Source:HGNC Symbol;Acc:HGNC:26335]","synonyms":"FLJ25333","biotype":"protein_coding","ncbi_id":"153643","summary":null,"start":95391344,"end":95450454,"strand":1,"description":"family with sequence similarity 81 member B [Source:HGNC Symbol;Acc:HGNC:26335]"}, {"versioned_ensembl_gene_id":"ENSG00000205060.10","gene_symbol":"SLC35B4","gene_name":"solute carrier family 35 member B4 [Source:HGNC Symbol;Acc:HGNC:20584]","synonyms":"YEA4,FLJ14697","biotype":"protein_coding","ncbi_id":"84912","summary":"Glycosyltransferases, such as SLC35B4, transport nucleotide sugars from the cytoplasm where they are synthesized, to the Golgi apparatus where they are utilized in the synthesis of glycoproteins, glycolipids, and proteoglycans (Ashikov et al., 2005 [PubMed 15911612]).[supplied by OMIM, Mar 2008]","start":134289332,"end":134317051,"strand":-1,"description":"solute carrier family 35 member B4 [Source:HGNC Symbol;Acc:HGNC:20584]"}, {"versioned_ensembl_gene_id":"ENSG00000244115.1","gene_symbol":"DNAJC25-GNG10","gene_name":"DNAJC25-GNG10 readthrough [Source:HGNC Symbol;Acc:HGNC:37501]","synonyms":null,"biotype":"protein_coding","ncbi_id":"552891","summary":"This gene represents naturally-occurring mRNAs that are co-transcribed products of the neighboring DNAJC25 and GNG10 genes. These transcripts include the first exon of DNAJC25 and the last two exons of GNG10, resulting in a protein that combines the N-terminus of DNAJC25 and the C-terminus of GNG10. [provided by RefSeq, Dec 2008]","start":111631386,"end":111670229,"strand":1,"description":"DNAJC25-GNG10 readthrough [Source:HGNC Symbol;Acc:HGNC:37501]"}, {"versioned_ensembl_gene_id":"ENSG00000182132.13","gene_symbol":"KCNIP1","gene_name":"potassium voltage-gated channel interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:15521]","synonyms":"KCHIP1","biotype":"protein_coding","ncbi_id":"30820","summary":"This gene encodes a member of the family of cytosolic voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the neuronal calcium sensor (NCS) family of the calcium binding EF-hand proteins. They associate with Kv4 alpha subunits to form native Kv4 channel complexes. The encoded protein may regulate rapidly inactivating (A-type) currents, and hence neuronal membrane excitability, in response to changes in the concentration of intracellular calcium. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":170353487,"end":170736632,"strand":1,"description":"potassium voltage-gated channel interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:15521]"}, {"versioned_ensembl_gene_id":"ENSG00000196890.4","gene_symbol":"HIST3H2BB","gene_name":"histone cluster 3 H2B family member b [Source:HGNC Symbol;Acc:HGNC:20514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128312","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":228458107,"end":228460470,"strand":1,"description":"histone cluster 3 H2B family member b [Source:HGNC Symbol;Acc:HGNC:20514]"}, {"versioned_ensembl_gene_id":"ENSG00000116198.12","gene_symbol":"CEP104","gene_name":"centrosomal protein 104 [Source:HGNC Symbol;Acc:HGNC:24866]","synonyms":"RP1-286D6.4,ROC22,KIAA0562,JBTS25,GlyBP,CFAP256","biotype":"protein_coding","ncbi_id":"9731","summary":"This gene encodes a centrosomal protein required for ciliogenesis and for ciliary tip structural integrity. The mammalian protein contains three amino-terminal hydrophobic domains, two glycosylation sites, four cysteine-rich motifs, and two regions with homology to the glutamate receptor ionotropic, NMDA 1 protein. During ciliogenesis, the encoded protein translocates from the distal tips of the centrioles to the tip of the elongating cilium. Knockdown of the protein in human retinal pigment cells results in severe defects in ciliogenesis with structural deformities at the ciliary tips. Allelic variants of this gene are associated with the autosomal-recessive disorder Joubert syndrome, which is characterized by a distinctive mid-hindbrain and cerebellar malformation, oculomotor apraxia, irregular breathing, developmental delay, and ataxia. [provided by RefSeq, Feb 2016]","start":3812081,"end":3857214,"strand":-1,"description":"centrosomal protein 104 [Source:HGNC Symbol;Acc:HGNC:24866]"}, {"versioned_ensembl_gene_id":"ENSG00000076248.10","gene_symbol":"UNG","gene_name":"uracil DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:12572]","synonyms":"UNG2,UNG1,UDG,HIGM4,DGU","biotype":"protein_coding","ncbi_id":"7374","summary":"This gene encodes one of several uracil-DNA glycosylases. One important function of uracil-DNA glycosylases is to prevent mutagenesis by eliminating uracil from DNA molecules by cleaving the N-glycosylic bond and initiating the base-excision repair (BER) pathway. Uracil bases occur from cytosine deamination or misincorporation of dUMP residues. Alternative promoter usage and splicing of this gene leads to two different isoforms: the mitochondrial UNG1 and the nuclear UNG2. The UNG2 term was used as a previous symbol for the CCNO gene (GeneID 10309), which has been confused with this gene, in the literature and some databases. [provided by RefSeq, Nov 2010]","start":109097574,"end":109110992,"strand":1,"description":"uracil DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:12572]"}, {"versioned_ensembl_gene_id":"ENSG00000276977.3","gene_symbol":"PDCD1","gene_name":"programmed cell death 1 [Source:HGNC Symbol;Acc:HGNC:8760]","synonyms":"SLEB2,PD1,PD-1,hSLE1,CD279","biotype":"protein_coding","ncbi_id":"5133","summary":"Programmed cell death protein 1 (PDCD1) is an immune-inhibitory receptor expressed in activated T cells; it is involved in the regulation of T-cell functions, including those of effector CD8+ T cells. In addition, this protein can also promote the differentiation of CD4+ T cells into T regulatory cells. PDCD1 is expressed in many types of tumors including melanomas, and has demonstrated to play a role in anti-tumor immunity. Moreover, this protein has been shown to be involved in safeguarding against autoimmunity, however, it can also contribute to the inhibition of effective anti-tumor and anti-microbial immunity. [provided by RefSeq, Aug 2020]","start":241849881,"end":241858908,"strand":-1,"description":"programmed cell death 1 [Source:HGNC Symbol;Acc:HGNC:8760]"}, {"versioned_ensembl_gene_id":"ENSG00000284729.1","gene_symbol":"AC006115.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56707293,"end":56791197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072121.15","gene_symbol":"ZFYVE26","gene_name":"zinc finger FYVE-type containing 26 [Source:HGNC Symbol;Acc:HGNC:20761]","synonyms":"SPG15,KIAA0321","biotype":"protein_coding","ncbi_id":"23503","summary":"This gene encodes a protein which contains a FYVE zinc finger binding domain. The presence of this domain is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. [provided by RefSeq, Oct 2008]","start":67727374,"end":67816590,"strand":-1,"description":"zinc finger FYVE-type containing 26 [Source:HGNC Symbol;Acc:HGNC:20761]"}, {"versioned_ensembl_gene_id":"ENSG00000258726.1","gene_symbol":"DUXAP6","gene_name":"double homeobox A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32185]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503635","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":92281484,"end":92282084,"strand":1,"description":"double homeobox A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32185]"}, {"versioned_ensembl_gene_id":"ENSG00000135093.12","gene_symbol":"USP30","gene_name":"ubiquitin specific peptidase 30 [Source:HGNC Symbol;Acc:HGNC:20065]","synonyms":"MGC10702,FLJ40511","biotype":"protein_coding","ncbi_id":"84749","summary":"USP30, a member of the ubiquitin-specific protease family (see USP1, MIM 603478), is a novel mitochondrial deubiquitinating (DUB) enzyme (Nakamura and Hirose, 2008 [PubMed 18287522]).[supplied by OMIM, Dec 2008]","start":109023089,"end":109088026,"strand":1,"description":"ubiquitin specific peptidase 30 [Source:HGNC Symbol;Acc:HGNC:20065]"}, {"versioned_ensembl_gene_id":"ENSG00000003147.17","gene_symbol":"ICA1","gene_name":"islet cell autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:5343]","synonyms":"ICAp69,ICA69","biotype":"protein_coding","ncbi_id":"3382","summary":"This gene encodes a protein with an arfaptin homology domain that is found both in the cytosol and as membrane-bound form on the Golgi complex and immature secretory granules. This protein is believed to be an autoantigen in insulin-dependent diabetes mellitus and primary Sjogren's syndrome. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":8113184,"end":8262687,"strand":-1,"description":"islet cell autoantigen 1 [Source:HGNC Symbol;Acc:HGNC:5343]"}, {"versioned_ensembl_gene_id":"ENSG00000232200.2","gene_symbol":"AL158090.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24297585,"end":24318086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250909.1","gene_symbol":"AC138956.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176347941,"end":176353584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167390.8","gene_symbol":"POM121L3P","gene_name":"POM121 transmembrane nucleoporin like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16440]","synonyms":"POM121L3,dJ831C21.3","biotype":"processed_pseudogene","ncbi_id":"651452","summary":null,"start":23989292,"end":23990454,"strand":1,"description":"POM121 transmembrane nucleoporin like 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:16440]"}, {"versioned_ensembl_gene_id":"ENSG00000226660.2","gene_symbol":"TRBV2","gene_name":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]","synonyms":"TCRBV22S1A2N1T,TCRBV2S1","biotype":"TR_V_gene","ncbi_id":"28620","summary":null,"start":142300924,"end":142301432,"strand":1,"description":"T-cell receptor beta variable 2 [Source:HGNC Symbol;Acc:HGNC:12195]"}, {"versioned_ensembl_gene_id":"ENSG00000185495.10","gene_symbol":"AC138393.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":223992743,"end":224010612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145220.13","gene_symbol":"LYAR","gene_name":"Ly1 antibody reactive [Source:HGNC Symbol;Acc:HGNC:26021]","synonyms":"ZLYAR,ZC2HC2","biotype":"protein_coding","ncbi_id":"55646","summary":null,"start":4267701,"end":4290169,"strand":-1,"description":"Ly1 antibody reactive [Source:HGNC Symbol;Acc:HGNC:26021]"}, {"versioned_ensembl_gene_id":"ENSG00000262634.5","gene_symbol":"SKA1","gene_name":"spindle and kinetochore associated complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28109]","synonyms":"MGC10200,C18orf24","biotype":"protein_coding","ncbi_id":"220134","summary":null,"start":50374995,"end":50394173,"strand":1,"description":"spindle and kinetochore associated complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28109]"}, {"versioned_ensembl_gene_id":"ENSG00000282443.1","gene_symbol":"AC105227.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50302190,"end":50313595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233431.1","gene_symbol":"AL359815.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21586472,"end":21591187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248320.1","gene_symbol":"THAP12P9","gene_name":"THAP domain containing 12 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39573]","synonyms":"PRKRIRP9","biotype":"processed_pseudogene","ncbi_id":"100131309","summary":null,"start":45323253,"end":45326028,"strand":-1,"description":"THAP domain containing 12 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39573]"}, {"versioned_ensembl_gene_id":"ENSG00000248987.2","gene_symbol":"PRDX4P1","gene_name":"peroxiredoxin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418949","summary":null,"start":44944015,"end":44944961,"strand":-1,"description":"peroxiredoxin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43598]"}, {"versioned_ensembl_gene_id":"ENSG00000205542.10","gene_symbol":"TMSB4X","gene_name":"thymosin beta 4, X-linked [Source:HGNC Symbol;Acc:HGNC:11881]","synonyms":"TMSB4,TB4X","biotype":"protein_coding","ncbi_id":"7114","summary":"This gene encodes an actin sequestering protein which plays a role in regulation of actin polymerization. The protein is also involved in cell proliferation, migration, and differentiation. This gene escapes X inactivation and has a homolog on chromosome Y. [provided by RefSeq, Jul 2008]","start":12975108,"end":12977227,"strand":1,"description":"thymosin beta 4, X-linked [Source:HGNC Symbol;Acc:HGNC:11881]"}, {"versioned_ensembl_gene_id":"ENSG00000183486.12","gene_symbol":"MX2","gene_name":"MX dynamin like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:7533]","synonyms":"MXB","biotype":"protein_coding","ncbi_id":"4600","summary":"The protein encoded by this gene has a nuclear and a cytoplasmic form and is a member of both the dynamin family and the family of large GTPases. The nuclear form is localized in a granular pattern in the heterochromatin region beneath the nuclear envelope. A nuclear localization signal (NLS) is present at the amino terminal end of the nuclear form but is lacking in the cytoplasmic form due to use of an alternate translation start codon. This protein is upregulated by interferon-alpha but does not contain the antiviral activity of a similar myxovirus resistance protein 1. [provided by RefSeq, Jul 2008]","start":41361943,"end":41409390,"strand":1,"description":"MX dynamin like GTPase 2 [Source:HGNC Symbol;Acc:HGNC:7533]"}, {"versioned_ensembl_gene_id":"ENSG00000144895.11","gene_symbol":"EIF2A","gene_name":"eukaryotic translation initiation factor 2A [Source:HGNC Symbol;Acc:HGNC:3254]","synonyms":"EIF-2A","biotype":"protein_coding","ncbi_id":"83939","summary":"This gene encodes a eukaryotic translation initiation factor that catalyzes the formation of puromycin-sensitive 80 S preinitiation complexes and the poly(U)-directed synthesis of polyphenylalanine at low concentrations of Mg2+. This gene should not be confused with eIF2-alpha (EIF2S1, Gene ID: 1965), the alpha subunit of the eIF2 translation initiation complex. Although both of these proteins function in binding initiator tRNA to the 40 S ribosomal subunit, the encoded protein does so in a codon-dependent manner, whereas eIF2 complex requires GTP. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":150546678,"end":150584242,"strand":1,"description":"eukaryotic translation initiation factor 2A [Source:HGNC Symbol;Acc:HGNC:3254]"}, {"versioned_ensembl_gene_id":"ENSG00000241336.1","gene_symbol":"LINC01487","gene_name":"long intergenic non-protein coding RNA 1487 [Source:HGNC Symbol;Acc:HGNC:51139]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928190","summary":null,"start":155240945,"end":155243144,"strand":1,"description":"long intergenic non-protein coding RNA 1487 [Source:HGNC Symbol;Acc:HGNC:51139]"}, {"versioned_ensembl_gene_id":"ENSG00000236435.1","gene_symbol":"TSPY12P","gene_name":"testis specific protein, Y-linked 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:23904]","synonyms":"TSPYP2","biotype":"unprocessed_pseudogene","ncbi_id":"377997","summary":null,"start":7687739,"end":7689548,"strand":-1,"description":"testis specific protein, Y-linked 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:23904]"}, {"versioned_ensembl_gene_id":"ENSG00000186163.9","gene_symbol":"TRY2P","gene_name":"trypsinogen-like pseudogene [Source:NCBI gene;Acc:207147]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"207147","summary":null,"start":142265833,"end":142272235,"strand":-1,"description":"trypsinogen-like pseudogene [Source:NCBI gene;Acc:207147]"}, {"versioned_ensembl_gene_id":"ENSG00000087263.16","gene_symbol":"OGFOD1","gene_name":"2-oxoglutarate and iron dependent oxygenase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25585]","synonyms":"TPA1,KIAA1612,FLJ10826","biotype":"protein_coding","ncbi_id":"55239","summary":null,"start":56451490,"end":56479100,"strand":1,"description":"2-oxoglutarate and iron dependent oxygenase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25585]"}, {"versioned_ensembl_gene_id":"ENSG00000170917.13","gene_symbol":"NUDT6","gene_name":"nudix hydrolase 6 [Source:HGNC Symbol;Acc:HGNC:8053]","synonyms":"gfg,gfg-1,FGF2AS,FGF-AS","biotype":"protein_coding","ncbi_id":"11162","summary":"This gene overlaps and lies on the opposite strand from FGF2 gene, and is thought to be the FGF2 antisense gene. The two genes are independently transcribed, and their expression shows an inverse relationship, suggesting that this antisense transcript may regulate FGF2 expression. This gene has also been shown to have hormone-regulatory and antiproliferative actions in the pituitary that are independent of FGF2 expression. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":122888697,"end":122922968,"strand":-1,"description":"nudix hydrolase 6 [Source:HGNC Symbol;Acc:HGNC:8053]"}, {"versioned_ensembl_gene_id":"ENSG00000254689.1","gene_symbol":"LINC02235","gene_name":"long intergenic non-protein coding RNA 2235 [Source:HGNC Symbol;Acc:HGNC:53106]","synonyms":"RP11-354A14.1","biotype":"lincRNA","ncbi_id":"109729147","summary":null,"start":81885377,"end":81923193,"strand":1,"description":"long intergenic non-protein coding RNA 2235 [Source:HGNC Symbol;Acc:HGNC:53106]"}, {"versioned_ensembl_gene_id":"ENSG00000135625.7","gene_symbol":"EGR4","gene_name":"early growth response 4 [Source:HGNC Symbol;Acc:HGNC:3241]","synonyms":"PAT133,NGFI-C","biotype":"protein_coding","ncbi_id":"1961","summary":null,"start":73290929,"end":73293705,"strand":-1,"description":"early growth response 4 [Source:HGNC Symbol;Acc:HGNC:3241]"}, {"versioned_ensembl_gene_id":"ENSG00000120742.10","gene_symbol":"SERP1","gene_name":"stress associated endoplasmic reticulum protein 1 [Source:HGNC Symbol;Acc:HGNC:10759]","synonyms":"RAMP4,FLJ43424","biotype":"protein_coding","ncbi_id":"27230","summary":null,"start":150541994,"end":150603228,"strand":-1,"description":"stress associated endoplasmic reticulum protein 1 [Source:HGNC Symbol;Acc:HGNC:10759]"}, {"versioned_ensembl_gene_id":"ENSG00000243058.1","gene_symbol":"AC015724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56573040,"end":56573195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101210.10","gene_symbol":"EEF1A2","gene_name":"eukaryotic translation elongation factor 1 alpha 2 [Source:HGNC Symbol;Acc:HGNC:3192]","synonyms":"STNL,STN,HS1,EEF1AL","biotype":"protein_coding","ncbi_id":"1917","summary":"This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 2) is expressed in brain, heart and skeletal muscle, and the other isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas. This gene may be critical in the development of ovarian cancer. [provided by RefSeq, Mar 2014]","start":63488013,"end":63499315,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 2 [Source:HGNC Symbol;Acc:HGNC:3192]"}, {"versioned_ensembl_gene_id":"ENSG00000279606.1","gene_symbol":"AC006600.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56471142,"end":56473647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270989.1","gene_symbol":"AC139493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176203314,"end":176203710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232900.1","gene_symbol":"AL050403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10875333,"end":10909272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234900.1","gene_symbol":"AL135937.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10753278,"end":10765286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172209.5","gene_symbol":"GPR22","gene_name":"G protein-coupled receptor 22 [Source:HGNC Symbol;Acc:HGNC:4477]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2845","summary":"This gene is a member of the G-protein coupled receptor 1 family and encodes a multi-pass membrane protein. [provided by RefSeq, Jul 2008]","start":107470018,"end":107475659,"strand":1,"description":"G protein-coupled receptor 22 [Source:HGNC Symbol;Acc:HGNC:4477]"}, {"versioned_ensembl_gene_id":"ENSG00000179818.13","gene_symbol":"PCBP1-AS1","gene_name":"PCBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42948]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"400960","summary":null,"start":69962263,"end":70103220,"strand":-1,"description":"PCBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42948]"}, {"versioned_ensembl_gene_id":"ENSG00000282414.1","gene_symbol":"IGHV3-62","gene_name":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28416","summary":null,"start":106667823,"end":106668266,"strand":-1,"description":"immunoglobulin heavy variable 3-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5615]"}, {"versioned_ensembl_gene_id":"ENSG00000232303.2","gene_symbol":"DFFBP1","gene_name":"DNA fragmentation factor subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49815]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422581","summary":null,"start":32566148,"end":32567126,"strand":-1,"description":"DNA fragmentation factor subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49815]"}, {"versioned_ensembl_gene_id":"ENSG00000171161.12","gene_symbol":"ZNF672","gene_name":"zinc finger protein 672 [Source:HGNC Symbol;Acc:HGNC:26179]","synonyms":"FLJ22301","biotype":"protein_coding","ncbi_id":"79894","summary":null,"start":248838210,"end":248849517,"strand":1,"description":"zinc finger protein 672 [Source:HGNC Symbol;Acc:HGNC:26179]"}, {"versioned_ensembl_gene_id":"ENSG00000106733.20","gene_symbol":"NMRK1","gene_name":"nicotinamide riboside kinase 1 [Source:HGNC Symbol;Acc:HGNC:26057]","synonyms":"NRK1,FLJ20559,C9orf95,bA235O14.2","biotype":"protein_coding","ncbi_id":"54981","summary":"Nicotinamide adenine dinucleotide (NAD+) is essential for life in all organisms, both as a coenzyme for oxidoreductases and as a source of ADP-ribosyl groups used in various reactions. Nicotinic acid and nicotinamide, collectively known as niacin, are the vitamin precursors of NAD+. Nicotinamide riboside kinases, such as NRK1, function to synthesize NAD+ through nicotinamide mononucleotide using nicotinamide riboside as the precursor (Bieganowski and Brenner, 2004 [PubMed 15137942]).[supplied by OMIM, Mar 2008]","start":75060573,"end":75088217,"strand":-1,"description":"nicotinamide riboside kinase 1 [Source:HGNC Symbol;Acc:HGNC:26057]"}, {"versioned_ensembl_gene_id":"ENSG00000226567.1","gene_symbol":"LINC00606","gene_name":"long intergenic non-protein coding RNA 606 [Source:HGNC Symbol;Acc:HGNC:43931]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285370","summary":null,"start":10759484,"end":10764192,"strand":-1,"description":"long intergenic non-protein coding RNA 606 [Source:HGNC Symbol;Acc:HGNC:43931]"}, {"versioned_ensembl_gene_id":"ENSG00000283366.1","gene_symbol":"AC000095.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18998274,"end":19014786,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282804.1","gene_symbol":"AL512428.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24797373,"end":24809798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112763.15","gene_symbol":"BTN2A1","gene_name":"butyrophilin subfamily 2 member A1 [Source:HGNC Symbol;Acc:HGNC:1136]","synonyms":"BTN2.1,BTF1,BT2.1","biotype":"protein_coding","ncbi_id":"11120","summary":"This gene encodes a member of the immunoglobulin superfamily. The gene is located in a cluster of butyrophilin-like genes in the juxta-telomeric region of the major histocompatibility complex on chromosome 6. A pseudogene of this gene has been identified in this cluster. The encoded protein is an integral plasma membrane protein involved in lipid, fatty-acid, and sterol metabolism. Alterations in this gene may be associated with several disease states including metabolic syndrome. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":26457904,"end":26476621,"strand":1,"description":"butyrophilin subfamily 2 member A1 [Source:HGNC Symbol;Acc:HGNC:1136]"}, {"versioned_ensembl_gene_id":"ENSG00000233485.1","gene_symbol":"AL031283.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15326680,"end":15343876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163012.3","gene_symbol":"ZSWIM2","gene_name":"zinc finger SWIM-type containing 2 [Source:HGNC Symbol;Acc:HGNC:30990]","synonyms":"ZZZ2,MGC33890","biotype":"protein_coding","ncbi_id":"151112","summary":null,"start":186827835,"end":186849208,"strand":-1,"description":"zinc finger SWIM-type containing 2 [Source:HGNC Symbol;Acc:HGNC:30990]"}, {"versioned_ensembl_gene_id":"ENSG00000276520.1","gene_symbol":"CR589904.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":248708202,"end":248708641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279301.4","gene_symbol":"OR2T11","gene_name":"olfactory receptor family 2 subfamily T member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19574]","synonyms":"OR2T11Q","biotype":"polymorphic_pseudogene","ncbi_id":"127077","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":248623557,"end":248635091,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19574]"}, {"versioned_ensembl_gene_id":"ENSG00000271701.1","gene_symbol":"AC098483.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":248601416,"end":248601869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273138.1","gene_symbol":"AC005021.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95416108,"end":95416462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229957.1","gene_symbol":"AL031687.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46168404,"end":46171237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187601.4","gene_symbol":"MAGEH1","gene_name":"MAGE family member H1 [Source:HGNC Symbol;Acc:HGNC:24092]","synonyms":"APR1","biotype":"protein_coding","ncbi_id":"28986","summary":"This gene belongs to the non-CT (non cancer/testis) subgroup of the melanoma-associated antigen (MAGE) superfamily. The encoded protein is likely associated with apoptosis, cell cycle arrest, growth inhibition or cell differentiation. The protein may be involved in the atRA (all-trans retinoic acid) signaling through the STAT1-alpha (signal transducer and activator of transcription 1-alpha) pathway. [provided by RefSeq, Aug 2013]","start":55452105,"end":55453566,"strand":1,"description":"MAGE family member H1 [Source:HGNC Symbol;Acc:HGNC:24092]"}, {"versioned_ensembl_gene_id":"ENSG00000261213.1","gene_symbol":"AC099786.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75122518,"end":75123927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277837.1","gene_symbol":"AC090340.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57427133,"end":57432112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282138.1","gene_symbol":"IGHV3-50","gene_name":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28422","summary":null,"start":106590798,"end":106591236,"strand":-1,"description":"immunoglobulin heavy variable 3-50 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5608]"}, {"versioned_ensembl_gene_id":"ENSG00000279631.1","gene_symbol":"AL158211.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":22252072,"end":22254589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196428.12","gene_symbol":"TSC22D2","gene_name":"TSC22 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:29095]","synonyms":"TILZ4b,TILZ4a,KIAA0669,TILZ4c","biotype":"protein_coding","ncbi_id":"9819","summary":null,"start":150408335,"end":150466431,"strand":1,"description":"TSC22 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:29095]"}, {"versioned_ensembl_gene_id":"ENSG00000233290.1","gene_symbol":"AC093580.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82215220,"end":82261133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240309.1","gene_symbol":"MTCO1P6","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075137","summary":null,"start":89588714,"end":89590097,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52008]"}, {"versioned_ensembl_gene_id":"ENSG00000260197.1","gene_symbol":"AC010889.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19691941,"end":19694606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279719.1","gene_symbol":"AC015871.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79989905,"end":79990606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271934.2","gene_symbol":"OR2AS2P","gene_name":"olfactory receptor family 2 subfamily AS member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31248]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403236","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248498308,"end":248498649,"strand":1,"description":"olfactory receptor family 2 subfamily AS member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31248]"}, {"versioned_ensembl_gene_id":"ENSG00000132832.10","gene_symbol":"LINC01260","gene_name":"long intergenic non-protein coding RNA 1260 [Source:HGNC Symbol;Acc:HGNC:49900]","synonyms":null,"biotype":"lincRNA","ncbi_id":"79015","summary":null,"start":44656451,"end":44696096,"strand":-1,"description":"long intergenic non-protein coding RNA 1260 [Source:HGNC Symbol;Acc:HGNC:49900]"}, {"versioned_ensembl_gene_id":"ENSG00000283440.1","gene_symbol":"AL139352.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44656451,"end":44663498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176299.5","gene_symbol":"OR4M1","gene_name":"olfactory receptor family 4 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14735]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441670","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19773504,"end":19783696,"strand":1,"description":"olfactory receptor family 4 subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:14735]"}, {"versioned_ensembl_gene_id":"ENSG00000277484.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738471,"end":54753005,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000066405.12","gene_symbol":"CLDN18","gene_name":"claudin 18 [Source:HGNC Symbol;Acc:HGNC:2039]","synonyms":"SFTPJ","biotype":"protein_coding","ncbi_id":"51208","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is upregulated in patients with ulcerative colitis and highly overexpressed in infiltrating ductal adenocarcinomas. PKC/MAPK/AP-1 (protein kinase C/mitogen-activated protein kinase/activator protein-1) dependent pathway regulates the expression of this gene in gastric cells. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2010]","start":137998735,"end":138033655,"strand":1,"description":"claudin 18 [Source:HGNC Symbol;Acc:HGNC:2039]"}, {"versioned_ensembl_gene_id":"ENSG00000224297.2","gene_symbol":"AL158825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74935176,"end":74935696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173258.12","gene_symbol":"ZNF483","gene_name":"zinc finger protein 483 [Source:HGNC Symbol;Acc:HGNC:23384]","synonyms":"ZSCAN48,ZKSCAN16,KIAA1962","biotype":"protein_coding","ncbi_id":"158399","summary":null,"start":111525159,"end":111577844,"strand":1,"description":"zinc finger protein 483 [Source:HGNC Symbol;Acc:HGNC:23384]"}, {"versioned_ensembl_gene_id":"ENSG00000170577.7","gene_symbol":"SIX2","gene_name":"SIX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:10888]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10736","summary":"This gene is a member of the vertebrate gene family which encode proteins homologous to the Drosophila 'sine oculis' homeobox protein. The encoded protein is a transcription factor which, like other members of this gene family, may be involved in limb or eye development. [provided by RefSeq, Dec 2008]","start":45005161,"end":45009430,"strand":-1,"description":"SIX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:10888]"}, {"versioned_ensembl_gene_id":"ENSG00000248143.1","gene_symbol":"LINC02383","gene_name":"long intergenic non-protein coding RNA 2383 [Source:HGNC Symbol;Acc:HGNC:53306]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374436","summary":null,"start":43457527,"end":43492543,"strand":-1,"description":"long intergenic non-protein coding RNA 2383 [Source:HGNC Symbol;Acc:HGNC:53306]"}, {"versioned_ensembl_gene_id":"ENSG00000282426.1","gene_symbol":"AC129507.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":356792,"end":358937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011638.10","gene_symbol":"TMEM159","gene_name":"transmembrane protein 159 [Source:HGNC Symbol;Acc:HGNC:30136]","synonyms":"promethin","biotype":"protein_coding","ncbi_id":"57146","summary":null,"start":21158377,"end":21180616,"strand":1,"description":"transmembrane protein 159 [Source:HGNC Symbol;Acc:HGNC:30136]"}, {"versioned_ensembl_gene_id":"ENSG00000137764.19","gene_symbol":"MAP2K5","gene_name":"mitogen-activated protein kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6845]","synonyms":"PRKMK5,MEK5,MAPKK5,HsT17454","biotype":"protein_coding","ncbi_id":"5607","summary":"The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase specifically interacts with and activates MAPK7/ERK5. This kinase itself can be phosphorylated and activated by MAP3K3/MEKK3, as well as by atypical protein kinase C isoforms (aPKCs). The signal cascade mediated by this kinase is involved in growth factor stimulated cell proliferation and muscle cell differentiation. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been described. [provided by RefSeq, May 2011]","start":67542709,"end":67807123,"strand":1,"description":"mitogen-activated protein kinase kinase 5 [Source:HGNC Symbol;Acc:HGNC:6845]"}, {"versioned_ensembl_gene_id":"ENSG00000160818.16","gene_symbol":"GPATCH4","gene_name":"G-patch domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25982]","synonyms":"GPATC4,FLJ20249,DKFZP434F1735","biotype":"protein_coding","ncbi_id":"54865","summary":null,"start":156594487,"end":156601496,"strand":-1,"description":"G-patch domain containing 4 [Source:HGNC Symbol;Acc:HGNC:25982]"}, {"versioned_ensembl_gene_id":"ENSG00000251517.1","gene_symbol":"AC096734.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42706107,"end":42707335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228684.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32884471,"end":32885407,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000267522.1","gene_symbol":"LINC01864","gene_name":"long intergenic non-protein coding RNA 1864 [Source:HGNC Symbol;Acc:HGNC:52683]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928886","summary":null,"start":56066684,"end":56078801,"strand":1,"description":"long intergenic non-protein coding RNA 1864 [Source:HGNC Symbol;Acc:HGNC:52683]"}, {"versioned_ensembl_gene_id":"ENSG00000229646.2","gene_symbol":"AL109914.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14597514,"end":14599690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257953.1","gene_symbol":"AC083805.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57837092,"end":57842745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108771.12","gene_symbol":"DHX58","gene_name":"DExH-box helicase 58 [Source:HGNC Symbol;Acc:HGNC:29517]","synonyms":"LGP2,D11LGP2","biotype":"protein_coding","ncbi_id":"79132","summary":null,"start":42101404,"end":42112733,"strand":-1,"description":"DExH-box helicase 58 [Source:HGNC Symbol;Acc:HGNC:29517]"}, {"versioned_ensembl_gene_id":"ENSG00000139053.2","gene_symbol":"PDE6H","gene_name":"phosphodiesterase 6H [Source:HGNC Symbol;Acc:HGNC:8790]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5149","summary":"This gene encodes the inhibitory (or gamma) subunit of the cone-specific cGMP phosphodiesterase, which is a tetramer composed of two catalytic chains (alpha and beta), and two inhibitory chains (gamma). It is specifically expressed in the retina, and is involved in the transmission and amplification of the visual signal. Mutations in this gene are associated with retinal cone dystrophy type 3A (RCD3A). [provided by RefSeq, Mar 2010]","start":14973022,"end":14981865,"strand":1,"description":"phosphodiesterase 6H [Source:HGNC Symbol;Acc:HGNC:8790]"}, {"versioned_ensembl_gene_id":"ENSG00000176728.7","gene_symbol":"TTTY14","gene_name":"testis-specific transcript, Y-linked 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18495]","synonyms":"TTY14,PRO2834,NCRNA00185,NCRNA00137,CYorf14","biotype":"lincRNA","ncbi_id":"83869","summary":null,"start":18872501,"end":19077416,"strand":-1,"description":"testis-specific transcript, Y-linked 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18495]"}, {"versioned_ensembl_gene_id":"ENSG00000119913.4","gene_symbol":"TECTB","gene_name":"tectorin beta [Source:HGNC Symbol;Acc:HGNC:11721]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6975","summary":"This gene encodes a non-collagenous glycoprotein component of the tectorial membrane, which covers the auditory hair cells in the cochlea of the inner ear. A similar protein in mouse functions in low-frequency hearing. [provided by RefSeq, Jul 2013]","start":112283735,"end":112305035,"strand":1,"description":"tectorin beta [Source:HGNC Symbol;Acc:HGNC:11721]"}, {"versioned_ensembl_gene_id":"ENSG00000177186.3","gene_symbol":"OR2M7","gene_name":"olfactory receptor family 2 subfamily M member 7 [Source:HGNC Symbol;Acc:HGNC:19594]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391196","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248323630,"end":248324568,"strand":-1,"description":"olfactory receptor family 2 subfamily M member 7 [Source:HGNC Symbol;Acc:HGNC:19594]"}, {"versioned_ensembl_gene_id":"ENSG00000226235.1","gene_symbol":"LEMD1-AS1","gene_name":"LEMD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44132]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"284576","summary":null,"start":205373252,"end":205387440,"strand":1,"description":"LEMD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44132]"}, {"versioned_ensembl_gene_id":"ENSG00000198788.8","gene_symbol":"MUC2","gene_name":"mucin 2, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7512]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"4583","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. The protein polymerizes into a gel of which 80% is composed of oligosaccharide side chains by weight. The protein features a central domain containing tandem repeats rich in threonine and proline that varies between 50 and 115 copies in different individuals. Downregulation of this gene has been observed in patients with Crohn disease and ulcerative colitis. [provided by RefSeq, Oct 2016]","start":1074875,"end":1110511,"strand":1,"description":"mucin 2, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7512]"}, {"versioned_ensembl_gene_id":"ENSG00000105851.10","gene_symbol":"PIK3CG","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:8978]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5294","summary":"Phosphoinositide 3-kinases (PI3Ks) phosphorylate inositol lipids and are involved in the immune response. The protein encoded by this gene is a class I catalytic subunit of PI3K. Like other class I catalytic subunits (p110-alpha p110-beta, and p110-delta), the encoded protein binds a p85 regulatory subunit to form PI3K. This gene is located in a commonly deleted segment of chromosome 7 previously identified in myeloid leukemias. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2015]","start":106865278,"end":106907145,"strand":1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:8978]"}, {"versioned_ensembl_gene_id":"ENSG00000260727.1","gene_symbol":"SLC7A5P1","gene_name":"solute carrier family 7 member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29458]","synonyms":"MLAS,LAT1-3TM","biotype":"unprocessed_pseudogene","ncbi_id":"81893","summary":"This locus represents a pseudogene of the L-type amino acid transporter 1. Transcripts initiating at this locus read through to downstream SMG1 pseudogene 2 (SMG1P2). [provided by RefSeq, Feb 2016]","start":29613104,"end":29613640,"strand":-1,"description":"solute carrier family 7 member 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29458]"}, {"versioned_ensembl_gene_id":"ENSG00000069869.15","gene_symbol":"NEDD4","gene_name":"neural precursor cell expressed, developmentally down-regulated 4, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:7727]","synonyms":"RPF1,NEDD4-1,MGC176705,KIAA0093","biotype":"protein_coding","ncbi_id":"4734","summary":"This gene is the founding member of the NEDD4 family of HECT ubiquitin ligases that function in the ubiquitin proteasome system of protein degradation. The encoded protein contains an N-terminal calcium and phospholipid binding C2 domain followed by multiple tryptophan-rich WW domains and, a C-terminal HECT ubiquitin ligase catalytic domain. It plays critical role in the regulation of a number of membrane receptors, endocytic machinery components and the tumor suppressor PTEN. [provided by RefSeq, Jul 2016]","start":55826922,"end":55993746,"strand":-1,"description":"neural precursor cell expressed, developmentally down-regulated 4, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:7727]"}, {"versioned_ensembl_gene_id":"ENSG00000282131.1","gene_symbol":"IGHV1-46","gene_name":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28465","summary":null,"start":106535796,"end":106536537,"strand":-1,"description":"immunoglobulin heavy variable 1-46 [Source:HGNC Symbol;Acc:HGNC:5554]"}, {"versioned_ensembl_gene_id":"ENSG00000260406.1","gene_symbol":"AC009852.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43302096,"end":43302772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196139.13","gene_symbol":"AKR1C3","gene_name":"aldo-keto reductase family 1 member C3 [Source:HGNC Symbol;Acc:HGNC:386]","synonyms":"PGFS,KIAA0119,HSD17B5,HAKRB,DDX","biotype":"protein_coding","ncbi_id":"8644","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme catalyzes the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ), and the oxidation of 9alpha,11beta-PGF2 to PGD2. It may play an important role in the pathogenesis of allergic diseases such as asthma, and may also have a role in controlling cell growth and/or differentiation. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":5035354,"end":5107686,"strand":1,"description":"aldo-keto reductase family 1 member C3 [Source:HGNC Symbol;Acc:HGNC:386]"}, {"versioned_ensembl_gene_id":"ENSG00000265644.1","gene_symbol":"AC087399.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78480549,"end":78484867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278488.2","gene_symbol":"NAPRT","gene_name":"nicotinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30450]","synonyms":"PP3856,NAPRT1","biotype":"protein_coding","ncbi_id":"93100","summary":"Nicotinic acid (NA; niacin) is converted by nicotinic acid phosphoribosyltransferase (NAPRT; EC 2.4.2.11) to NA mononucleotide (NaMN), which is then converted to NA adenine dinucleotide (NaAD), and finally to nicotinamide adenine dinucleotide (NAD), which serves as a coenzyme in cellular redox reactions and is an essential component of a variety of processes in cellular metabolism including response to stress (Hara et al., 2007).[supplied by OMIM, Mar 2008]","start":143574785,"end":143578649,"strand":-1,"description":"nicotinate phosphoribosyltransferase [Source:HGNC Symbol;Acc:HGNC:30450]"}, {"versioned_ensembl_gene_id":"ENSG00000254830.1","gene_symbol":"AP002428.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98938912,"end":98945079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111897.6","gene_symbol":"SERINC1","gene_name":"serine incorporator 1 [Source:HGNC Symbol;Acc:HGNC:13464]","synonyms":"TMS-2,TDE2,TDE1L,KIAA1253","biotype":"protein_coding","ncbi_id":"57515","summary":null,"start":122443354,"end":122471822,"strand":-1,"description":"serine incorporator 1 [Source:HGNC Symbol;Acc:HGNC:13464]"}, {"versioned_ensembl_gene_id":"ENSG00000272984.1","gene_symbol":"AC007349.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36734004,"end":36734535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271396.1","gene_symbol":"AC091167.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90284376,"end":90285580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249145.1","gene_symbol":"LINC02517","gene_name":"long intergenic non-protein coding RNA 2517 [Source:HGNC Symbol;Acc:HGNC:53506]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374374","summary":null,"start":8320176,"end":8323863,"strand":1,"description":"long intergenic non-protein coding RNA 2517 [Source:HGNC Symbol;Acc:HGNC:53506]"}, {"versioned_ensembl_gene_id":"ENSG00000225255.6","gene_symbol":"LINC01297","gene_name":"long intergenic non-protein coding RNA 1297 [Source:NCBI gene;Acc:106146148]","synonyms":"LA16c-83F12.6","biotype":"lincRNA","ncbi_id":"106146148","summary":null,"start":15746630,"end":15778297,"strand":1,"description":"long intergenic non-protein coding RNA 1297 [Source:NCBI gene;Acc:106146148]"}, {"versioned_ensembl_gene_id":"ENSG00000162623.15","gene_symbol":"TYW3","gene_name":"tRNA-yW synthesizing protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:24757]","synonyms":"FLJ40918,C1orf171","biotype":"protein_coding","ncbi_id":"127253","summary":"Wybutosine (yW) is a hypermodified guanosine at the 3-prime position adjacent to the anticodon of phenylalanine tRNA that stabilizes codon-anticodon interactions during decoding on the ribosome. TYW3 is the human homolog of a yeast gene essential for yW synthesis (Noma and Suzuki, 2006).[supplied by OMIM, Mar 2008]","start":74733152,"end":74766678,"strand":1,"description":"tRNA-yW synthesizing protein 3 homolog [Source:HGNC Symbol;Acc:HGNC:24757]"}, {"versioned_ensembl_gene_id":"ENSG00000253314.5","gene_symbol":"LINC00293","gene_name":"long intergenic non-protein coding RNA 293 [Source:HGNC Symbol;Acc:HGNC:39078]","synonyms":"NCRNA00293,BEYLA","biotype":"lincRNA","ncbi_id":"497634","summary":null,"start":46822237,"end":46854307,"strand":1,"description":"long intergenic non-protein coding RNA 293 [Source:HGNC Symbol;Acc:HGNC:39078]"}, {"versioned_ensembl_gene_id":"ENSG00000284626.1","gene_symbol":"AC091167.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":90234200,"end":90265462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278875.1","gene_symbol":"AC025809.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31364297,"end":31366098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063245.14","gene_symbol":"EPN1","gene_name":"epsin 1 [Source:HGNC Symbol;Acc:HGNC:21604]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29924","summary":"This gene encodes a member of the epsin protein family. The encoded protein binds clathrin and is involved in the endocytosis of clathrin-coated vesicles. Loss of function of this gene is associated with reduced tumor growth and progression in certain cancer types. [provided by RefSeq, Mar 2016]","start":55675226,"end":55709858,"strand":1,"description":"epsin 1 [Source:HGNC Symbol;Acc:HGNC:21604]"}, {"versioned_ensembl_gene_id":"ENSG00000261420.1","gene_symbol":"AL022069.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":166383189,"end":166384824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103978.15","gene_symbol":"TMEM87A","gene_name":"transmembrane protein 87A [Source:HGNC Symbol;Acc:HGNC:24522]","synonyms":"DKFZP564G2022","biotype":"protein_coding","ncbi_id":"25963","summary":null,"start":42210452,"end":42273663,"strand":-1,"description":"transmembrane protein 87A [Source:HGNC Symbol;Acc:HGNC:24522]"}, {"versioned_ensembl_gene_id":"ENSG00000243667.6","gene_symbol":"WDR92","gene_name":"WD repeat domain 92 [Source:HGNC Symbol;Acc:HGNC:25176]","synonyms":"Monad,FLJ31741","biotype":"protein_coding","ncbi_id":"116143","summary":"This gene encodes a protein with two WD40 repeat domains thought to be involved in an apoptosis via activation of caspase-3. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":68122936,"end":68157560,"strand":-1,"description":"WD repeat domain 92 [Source:HGNC Symbol;Acc:HGNC:25176]"}, {"versioned_ensembl_gene_id":"ENSG00000260332.1","gene_symbol":"AC010546.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62808222,"end":62808706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228294.6","gene_symbol":"BMS1P17","gene_name":"BMS1, ribosome biogenesis factor pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49162]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101101776","summary":null,"start":19301704,"end":19316914,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49162]"}, {"versioned_ensembl_gene_id":"ENSG00000229621.1","gene_symbol":"LINC01822","gene_name":"long intergenic non-protein coding RNA 1822 [Source:HGNC Symbol;Acc:HGNC:52627]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645949","summary":null,"start":21687434,"end":21710623,"strand":-1,"description":"long intergenic non-protein coding RNA 1822 [Source:HGNC Symbol;Acc:HGNC:52627]"}, {"versioned_ensembl_gene_id":"ENSG00000013503.9","gene_symbol":"POLR3B","gene_name":"RNA polymerase III subunit B [Source:HGNC Symbol;Acc:HGNC:30348]","synonyms":"RPC2,FLJ10388","biotype":"protein_coding","ncbi_id":"55703","summary":"This gene encodes the second largest subunit of RNA polymerase III, the polymerase responsible for synthesizing transfer and small ribosomal RNAs in eukaryotes. The largest subunit and the encoded protein form the catalytic center of RNA polymerase III. Mutations in this gene are a cause of hypomyelinating leukodystrophy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":106357658,"end":106510198,"strand":1,"description":"RNA polymerase III subunit B [Source:HGNC Symbol;Acc:HGNC:30348]"}, {"versioned_ensembl_gene_id":"ENSG00000169224.12","gene_symbol":"GCSAML","gene_name":"germinal center associated signaling and motility like [Source:HGNC Symbol;Acc:HGNC:29583]","synonyms":"FLJ44728,C1orf150","biotype":"protein_coding","ncbi_id":"148823","summary":"This gene encodes a protein thought to be a signaling molecule associated with germinal centers, the sites of proliferation and differentiation of mature B lymphocytes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":247507058,"end":247577690,"strand":1,"description":"germinal center associated signaling and motility like [Source:HGNC Symbol;Acc:HGNC:29583]"}, {"versioned_ensembl_gene_id":"ENSG00000241418.1","gene_symbol":"MCRIP2P1","gene_name":"MAPK regulated corepressor interacting protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49629]","synonyms":"FAM195CP","biotype":"processed_pseudogene","ncbi_id":"102388891","summary":null,"start":131795657,"end":131796167,"strand":-1,"description":"MAPK regulated corepressor interacting protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49629]"}, {"versioned_ensembl_gene_id":"ENSG00000279662.1","gene_symbol":"AC131649.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10445309,"end":10449747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113558.18","gene_symbol":"SKP1","gene_name":"S-phase kinase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10899]","synonyms":"TCEB1L,SKP1A,p19A,OCP2,OCP-II,MGC34403,EMC19","biotype":"protein_coding","ncbi_id":"6500","summary":"This gene encodes a component of SCF complexes, which are composed of this protein, cullin 1, a ring-box protein, and one member of the F-box family of proteins. This protein binds directly to the F-box motif found in F-box proteins. SCF complexes are involved in the regulated ubiquitination of specific protein substrates, which targets them for degradation by the proteosome. Specific F-box proteins recognize different target protein(s), and many specific SCF substrates have been identified including regulators of cell cycle progression and development. Studies have also characterized the protein as an RNA polymerase II elongation factor. Alternative splicing of this gene results in two transcript variants. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Jul 2008]","start":134148935,"end":134177038,"strand":-1,"description":"S-phase kinase associated protein 1 [Source:HGNC Symbol;Acc:HGNC:10899]"}, {"versioned_ensembl_gene_id":"ENSG00000214321.3","gene_symbol":"CBX1P4","gene_name":"chromobox 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38658]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130461","summary":null,"start":17282637,"end":17283093,"strand":1,"description":"chromobox 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38658]"}, {"versioned_ensembl_gene_id":"ENSG00000281519.1","gene_symbol":"AC093642.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242099909,"end":242121247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277783.1","gene_symbol":"AL078601.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79464740,"end":79464999,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280943.1","gene_symbol":"AC093642.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242052699,"end":242089153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281268.1","gene_symbol":"AC244167.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242030199,"end":242031170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125814.17","gene_symbol":"NAPB","gene_name":"NSF attachment protein beta [Source:HGNC Symbol;Acc:HGNC:15751]","synonyms":"SNAPB,SNAP-BETA","biotype":"protein_coding","ncbi_id":"63908","summary":"This gene encodes a member of the soluble N-ethyl-maleimide-sensitive fusion attachment protein (SNAP) family. SNAP proteins play a critical role in the docking and fusion of vesicles to target membranes as part of the 20S NSF-SNAP-SNARE complex. This gene encodes the SNAP beta isoform which has been shown to be preferentially expressed in brain tissue. The encoded protein also interacts with the GluR2 α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptor subunit C-terminus and may play a role as a chaperone in the molecular processing of the AMPA receptor. [provided by RefSeq, Mar 2017]","start":23374519,"end":23421519,"strand":-1,"description":"NSF attachment protein beta [Source:HGNC Symbol;Acc:HGNC:15751]"}, {"versioned_ensembl_gene_id":"ENSG00000161835.10","gene_symbol":"GRASP","gene_name":"general receptor for phosphoinositides 1 associated scaffold protein [Source:HGNC Symbol;Acc:HGNC:18707]","synonyms":"Tamalin","biotype":"protein_coding","ncbi_id":"160622","summary":"This gene encodes a protein that functions as a molecular scaffold, linking receptors, including group 1 metabotropic glutamate receptors, to neuronal proteins. The encoded protein contains conserved domains, including a leucine zipper sequence, PDZ domain and a C-terminal PDZ-binding motif. Alternately spliced transcript variants have been observed for this gene.[provided by RefSeq, Dec 2012]","start":52006940,"end":52015889,"strand":1,"description":"general receptor for phosphoinositides 1 associated scaffold protein [Source:HGNC Symbol;Acc:HGNC:18707]"}, {"versioned_ensembl_gene_id":"ENSG00000235992.1","gene_symbol":"GRAMD4P2","gene_name":"GRAM domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873881","summary":null,"start":15749156,"end":15750825,"strand":-1,"description":"GRAM domain containing 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39654]"}, {"versioned_ensembl_gene_id":"ENSG00000177453.7","gene_symbol":"NIM1K","gene_name":"NIM1 serine/threonine protein kinase [Source:HGNC Symbol;Acc:HGNC:28646]","synonyms":"NIM1,MGC42105","biotype":"protein_coding","ncbi_id":"167359","summary":null,"start":43192071,"end":43280850,"strand":1,"description":"NIM1 serine/threonine protein kinase [Source:HGNC Symbol;Acc:HGNC:28646]"}, {"versioned_ensembl_gene_id":"ENSG00000198062.14","gene_symbol":"POTEH","gene_name":"POTE ankyrin domain family member H [Source:HGNC Symbol;Acc:HGNC:133]","synonyms":"POTE22,CT104.7,ACTBL1,A26C3","biotype":"protein_coding","ncbi_id":"23784","summary":null,"start":15690026,"end":15721631,"strand":1,"description":"POTE ankyrin domain family member H [Source:HGNC Symbol;Acc:HGNC:133]"}, {"versioned_ensembl_gene_id":"ENSG00000005022.5","gene_symbol":"SLC25A5","gene_name":"solute carrier family 25 member 5 [Source:HGNC Symbol;Acc:HGNC:10991]","synonyms":"T3,T2,ANT2,2F1","biotype":"protein_coding","ncbi_id":"292","summary":"This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Suppressed expression of this gene has been shown to induce apoptosis and inhibit tumor growth. The human genome contains several non-transcribed pseudogenes of this gene.[provided by RefSeq, Jun 2013]","start":119468400,"end":119471319,"strand":1,"description":"solute carrier family 25 member 5 [Source:HGNC Symbol;Acc:HGNC:10991]"}, {"versioned_ensembl_gene_id":"ENSG00000266830.1","gene_symbol":"AC061975.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28246454,"end":28248006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272040.1","gene_symbol":"AC010245.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75608817,"end":75609983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138448.11","gene_symbol":"ITGAV","gene_name":"integrin subunit alpha V [Source:HGNC Symbol;Acc:HGNC:6150]","synonyms":"VTNR,VNRA,MSK8,CD51","biotype":"protein_coding","ncbi_id":"3685","summary":"The product of this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha subunit and a beta subunit that function in cell surface adhesion and signaling. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha V subunit. This subunit associates with beta 1, beta 3, beta 5, beta 6 and beta 8 subunits. The heterodimer consisting of alpha V and beta 3 subunits is also known as the vitronectin receptor. This integrin may regulate angiogenesis and cancer progression. Alternative splicing results in multiple transcript variants. Note that the integrin alpha 5 and integrin alpha V subunits are encoded by distinct genes. [provided by RefSeq, Oct 2015]","start":186590065,"end":186680901,"strand":1,"description":"integrin subunit alpha V [Source:HGNC Symbol;Acc:HGNC:6150]"}, {"versioned_ensembl_gene_id":"ENSG00000218574.1","gene_symbol":"HNRNPA1P37","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:48766]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421379","summary":null,"start":5609227,"end":5610195,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:48766]"}, {"versioned_ensembl_gene_id":"ENSG00000068028.17","gene_symbol":"RASSF1","gene_name":"Ras association domain family member 1 [Source:HGNC Symbol;Acc:HGNC:9882]","synonyms":"REH3P21,RDA32,NORE2A,123F2","biotype":"protein_coding","ncbi_id":"11186","summary":"This gene encodes a protein similar to the RAS effector proteins. Loss or altered expression of this gene has been associated with the pathogenesis of a variety of cancers, which suggests the tumor suppressor function of this gene. The inactivation of this gene was found to be correlated with the hypermethylation of its CpG-island promoter region. The encoded protein was found to interact with DNA repair protein XPA. The protein was also shown to inhibit the accumulation of cyclin D1, and thus induce cell cycle arrest. Several alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, May 2011]","start":50329782,"end":50340980,"strand":-1,"description":"Ras association domain family member 1 [Source:HGNC Symbol;Acc:HGNC:9882]"}, {"versioned_ensembl_gene_id":"ENSG00000015520.14","gene_symbol":"NPC1L1","gene_name":"NPC1 like intracellular cholesterol transporter 1 [Source:HGNC Symbol;Acc:HGNC:7898]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29881","summary":"The protein encoded by this gene is a multi-pass membrane protein. It contains a conserved N-terminal Niemann-Pick C1 (NPC1) domain and a putative sterol-sensing domain (SSD) which includes a YQRL motif functioning as a plasma membrane to trans-Golgi network transport signal in other proteins. This protein takes up free cholesterol into cells through vesicular endocytosis and plays a critical role in the absorption of intestinal cholesterol. It also has the ability to transport alpha-tocopherol (vitamin E). The drug ezetimibe targets this protein and inhibits the absorption of intestinal cholesterol and alpha-tocopherol. In addition, this protein may play a critical role in regulating lipid metabolism. Polymorphic variations in this gene are associated with plasma total cholesterol and low-density lipoprotein cholesterol (LDL-C) levels and coronary heart disease (CHD) risk. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":44512535,"end":44541315,"strand":-1,"description":"NPC1 like intracellular cholesterol transporter 1 [Source:HGNC Symbol;Acc:HGNC:7898]"}, {"versioned_ensembl_gene_id":"ENSG00000133069.15","gene_symbol":"TMCC2","gene_name":"transmembrane and coiled-coil domain family 2 [Source:HGNC Symbol;Acc:HGNC:24239]","synonyms":"HUCEP11,FLJ38497","biotype":"protein_coding","ncbi_id":"9911","summary":null,"start":205228176,"end":205273343,"strand":1,"description":"transmembrane and coiled-coil domain family 2 [Source:HGNC Symbol;Acc:HGNC:24239]"}, {"versioned_ensembl_gene_id":"ENSG00000234590.1","gene_symbol":"GNG5P5","gene_name":"G protein subunit gamma 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100101935","summary":null,"start":47307082,"end":47307301,"strand":1,"description":"G protein subunit gamma 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33554]"}, {"versioned_ensembl_gene_id":"ENSG00000269924.1","gene_symbol":"AC024451.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47527397,"end":47528148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254065.1","gene_symbol":"AC024451.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47592147,"end":47592609,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227540.1","gene_symbol":"DNAJC9-AS1","gene_name":"DNAJC9 antisense RNA 1 [Source:NCBI gene;Acc:414245]","synonyms":"C10orf103,bA537A6.3,C10orf103,bA537A6.3","biotype":"antisense_RNA","ncbi_id":"414245","summary":null,"start":73252791,"end":73254349,"strand":1,"description":"DNAJC9 antisense RNA 1 [Source:NCBI gene;Acc:414245]"}, {"versioned_ensembl_gene_id":"ENSG00000269918.1","gene_symbol":"AF131215.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11104691,"end":11106704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187186.14","gene_symbol":"AL162231.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34664163,"end":34666112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187952.9","gene_symbol":"HS6ST1P1","gene_name":"heparan sulfate 6-O-sulfotransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31835]","synonyms":"HS6ST1P","biotype":"processed_pseudogene","ncbi_id":"388605","summary":null,"start":21428303,"end":21429536,"strand":1,"description":"heparan sulfate 6-O-sulfotransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31835]"}, {"versioned_ensembl_gene_id":"ENSG00000255310.2","gene_symbol":"AF131215.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11107788,"end":11109726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254936.4","gene_symbol":"AF131215.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11123381,"end":11126064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213872.3","gene_symbol":"AC092798.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25749488,"end":25749896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230602.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32466666,"end":32469843,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000116754.13","gene_symbol":"SRSF11","gene_name":"serine and arginine rich splicing factor 11 [Source:HGNC Symbol;Acc:HGNC:10782]","synonyms":"SFRS11,p54,NET2","biotype":"protein_coding","ncbi_id":"9295","summary":"This gene encodes 54-kD nuclear protein that contains an arginine/serine-rich region similar to segments found in pre-mRNA splicing factors. Although the function of this protein is not yet known, structure and immunolocalization data suggest that it may play a role in pre-mRNA processing. Alternative splicing results in multiple transcript variants encoding different proteins. In addition, a pseudogene of this gene has been found on chromosome 12.[provided by RefSeq, Sep 2010]","start":70205682,"end":70253052,"strand":1,"description":"serine and arginine rich splicing factor 11 [Source:HGNC Symbol;Acc:HGNC:10782]"}, {"versioned_ensembl_gene_id":"ENSG00000246375.2","gene_symbol":"AC107067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88284942,"end":88331421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229660.1","gene_symbol":"AC004975.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157281536,"end":157282686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225237.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32401725,"end":32402684,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000276482.3","gene_symbol":"SLC12A7","gene_name":"solute carrier family 12 member 7 [Source:HGNC Symbol;Acc:HGNC:10915]","synonyms":"DKFZP434F076,KCC4","biotype":"protein_coding","ncbi_id":"10723","summary":null,"start":1050378,"end":1111210,"strand":-1,"description":"solute carrier family 12 member 7 [Source:HGNC Symbol;Acc:HGNC:10915]"}, {"versioned_ensembl_gene_id":"ENSG00000130511.15","gene_symbol":"SSBP4","gene_name":"single stranded DNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:15676]","synonyms":null,"biotype":"protein_coding","ncbi_id":"170463","summary":null,"start":18418864,"end":18434562,"strand":1,"description":"single stranded DNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:15676]"}, {"versioned_ensembl_gene_id":"ENSG00000271696.1","gene_symbol":"AC023141.13","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57835309,"end":57836251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183801.7","gene_symbol":"OLFML1","gene_name":"olfactomedin like 1 [Source:HGNC Symbol;Acc:HGNC:24473]","synonyms":"UNQ564","biotype":"protein_coding","ncbi_id":"283298","summary":null,"start":7485388,"end":7511377,"strand":1,"description":"olfactomedin like 1 [Source:HGNC Symbol;Acc:HGNC:24473]"}, {"versioned_ensembl_gene_id":"ENSG00000231232.4","gene_symbol":"AC023141.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57822465,"end":57822801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253500.5","gene_symbol":"AF121898.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87540835,"end":87755718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234396.3","gene_symbol":"AL590822.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2212523,"end":2220738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241224.7","gene_symbol":"C3orf85","gene_name":"chromosome 3 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:53432]","synonyms":"FLJ22763","biotype":"protein_coding","ncbi_id":"401081","summary":null,"start":109118252,"end":109150514,"strand":1,"description":"chromosome 3 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:53432]"}, {"versioned_ensembl_gene_id":"ENSG00000260426.1","gene_symbol":"AC008060.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":155399922,"end":155401782,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256810.1","gene_symbol":"AC078925.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131030570,"end":131035487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278570.4","gene_symbol":"NR2E3","gene_name":"nuclear receptor subfamily 2 group E member 3 [Source:HGNC Symbol;Acc:HGNC:7974]","synonyms":"RP37,rd7,PNR","biotype":"protein_coding","ncbi_id":"10002","summary":"This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":71792638,"end":71818259,"strand":1,"description":"nuclear receptor subfamily 2 group E member 3 [Source:HGNC Symbol;Acc:HGNC:7974]"}, {"versioned_ensembl_gene_id":"ENSG00000101349.16","gene_symbol":"PAK5","gene_name":"p21 (RAC1) activated kinase 5 [Source:HGNC Symbol;Acc:HGNC:15916]","synonyms":"PAK7,KIAA1264","biotype":"protein_coding","ncbi_id":"57144","summary":"The protein encoded by this gene is a member of the PAK family of Ser/Thr protein kinases. PAK family members are known to be effectors of Rac/Cdc42 GTPases, which have been implicated in the regulation of cytoskeletal dynamics, proliferation, and cell survival signaling. This kinase contains a CDC42/Rac1 interactive binding (CRIB) motif, and has been shown to bind CDC42 in the presence of GTP. This kinase is predominantly expressed in brain. It is capable of promoting neurite outgrowth, and thus may play a role in neurite development. This kinase is associated with microtubule networks and induces microtubule stabilization. The subcellular localization of this kinase is tightly regulated during cell cycle progression. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":9537389,"end":9839041,"strand":-1,"description":"p21 (RAC1) activated kinase 5 [Source:HGNC Symbol;Acc:HGNC:15916]"}, {"versioned_ensembl_gene_id":"ENSG00000011566.14","gene_symbol":"MAP4K3","gene_name":"mitogen-activated protein kinase kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6865]","synonyms":"RAB8IPL1,MAPKKKK3,GLK","biotype":"protein_coding","ncbi_id":"8491","summary":"This gene encodes a member of the mitogen-activated protein kinase kinase kinase kinase family. The encoded protein activates key effectors in cell signalling, among them c-Jun. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":39249266,"end":39437312,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 3 [Source:HGNC Symbol;Acc:HGNC:6865]"}, {"versioned_ensembl_gene_id":"ENSG00000273992.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1,CLR19.9,NBS1,FLJ20510,PAN1","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54961245,"end":55009257,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000275179.1","gene_symbol":"AL118508.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23180176,"end":23187544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228611.2","gene_symbol":"HNF4GP1","gene_name":"hepatocyte nuclear factor 4 gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35417]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130462","summary":null,"start":55999200,"end":56000448,"strand":-1,"description":"hepatocyte nuclear factor 4 gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35417]"}, {"versioned_ensembl_gene_id":"ENSG00000215085.4","gene_symbol":"AL365400.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95584303,"end":95584942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271094.1","gene_symbol":"AL022161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95453369,"end":95453581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013016.15","gene_symbol":"EHD3","gene_name":"EH domain containing 3 [Source:HGNC Symbol;Acc:HGNC:3244]","synonyms":"PAST3","biotype":"protein_coding","ncbi_id":"30845","summary":null,"start":31234337,"end":31269447,"strand":1,"description":"EH domain containing 3 [Source:HGNC Symbol;Acc:HGNC:3244]"}, {"versioned_ensembl_gene_id":"ENSG00000271580.1","gene_symbol":"AL583832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205091163,"end":205091946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147145.12","gene_symbol":"LPAR4","gene_name":"lysophosphatidic acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:4478]","synonyms":"P2Y9,P2Y5-LIKE,P2RY9,LPA4,GPR23","biotype":"protein_coding","ncbi_id":"2846","summary":"This gene encodes a member of the lysophosphatidic acid receptor family. It may also be related to the P2Y receptors, a family of receptors that bind purine and pyrimidine nucleotides and are coupled to G proteins. The encoded protein may play a role in monocytic differentiation. [provided by RefSeq, Feb 2009]","start":78747709,"end":78757094,"strand":1,"description":"lysophosphatidic acid receptor 4 [Source:HGNC Symbol;Acc:HGNC:4478]"}, {"versioned_ensembl_gene_id":"ENSG00000258150.5","gene_symbol":"AC133555.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29464967,"end":29467833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000035664.11","gene_symbol":"DAPK2","gene_name":"death associated protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:2675]","synonyms":"MGC119312,DRP-1","biotype":"protein_coding","ncbi_id":"23604","summary":"This gene encodes a protein that belongs to the serine/threonine protein kinase family. This protein contains a N-terminal protein kinase domain followed by a conserved calmodulin-binding domain with significant similarity to that of death-associated protein kinase 1 (DAPK1), a positive regulator of programmed cell death. Overexpression of this gene was shown to induce cell apoptosis. It uses multiple polyadenylation sites. [provided by RefSeq, Jul 2008]","start":63907036,"end":64072033,"strand":-1,"description":"death associated protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:2675]"}, {"versioned_ensembl_gene_id":"ENSG00000277579.1","gene_symbol":"AC244093.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37034668,"end":37043252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279100.1","gene_symbol":"AC009120.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74150520,"end":74151299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282659.1","gene_symbol":"SLC20A1P2","gene_name":"solute carrier family 20 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"192128","summary":null,"start":106180325,"end":106181290,"strand":-1,"description":"solute carrier family 20 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42539]"}, {"versioned_ensembl_gene_id":"ENSG00000231153.1","gene_symbol":"AC002429.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95018407,"end":95018554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270067.1","gene_symbol":"AC008536.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112893333,"end":112894001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275636.1","gene_symbol":"AC021755.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40078892,"end":40079347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108651.9","gene_symbol":"UTP6","gene_name":"UTP6, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:18279]","synonyms":"HCA66,C17orf40","biotype":"protein_coding","ncbi_id":"55813","summary":null,"start":31860899,"end":31901765,"strand":-1,"description":"UTP6, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:18279]"}, {"versioned_ensembl_gene_id":"ENSG00000225347.1","gene_symbol":"SLC25A5P8","gene_name":"solute carrier family 25 member 5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35469]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392301","summary":null,"start":32333457,"end":32334354,"strand":-1,"description":"solute carrier family 25 member 5 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35469]"}, {"versioned_ensembl_gene_id":"ENSG00000141867.17","gene_symbol":"BRD4","gene_name":"bromodomain containing 4 [Source:HGNC Symbol;Acc:HGNC:13575]","synonyms":"MCAP,HUNKI,HUNK1,CAP","biotype":"protein_coding","ncbi_id":"23476","summary":"The protein encoded by this gene is homologous to the murine protein MCAP, which associates with chromosomes during mitosis, and to the human RING3 protein, a serine/threonine kinase. Each of these proteins contains two bromodomains, a conserved sequence motif which may be involved in chromatin targeting. This gene has been implicated as the chromosome 19 target of translocation t(15;19)(q13;p13.1), which defines an upper respiratory tract carcinoma in young people. Two alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]","start":15235519,"end":15332545,"strand":-1,"description":"bromodomain containing 4 [Source:HGNC Symbol;Acc:HGNC:13575]"}, {"versioned_ensembl_gene_id":"ENSG00000226446.1","gene_symbol":"NOTCH2P1","gene_name":"notch 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44253]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420260","summary":null,"start":119886304,"end":119886927,"strand":1,"description":"notch 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44253]"}, {"versioned_ensembl_gene_id":"ENSG00000284683.1","gene_symbol":"AC087565.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73318240,"end":73891752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229126.5","gene_symbol":"BX248321.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31002649,"end":31027602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227205.4","gene_symbol":"PFN1P9","gene_name":"profilin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42991]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"767850","summary":null,"start":119853316,"end":119853748,"strand":1,"description":"profilin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42991]"}, {"versioned_ensembl_gene_id":"ENSG00000260848.1","gene_symbol":"AC092114.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73543941,"end":73558522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282569.1","gene_symbol":"IGHVIII-13-1","gene_name":"immunoglobulin heavy variable (III)-13-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5693]","synonyms":"IGHV(III)-13-1","biotype":"IG_V_pseudogene","ncbi_id":"28351","summary":null,"start":106143058,"end":106143348,"strand":-1,"description":"immunoglobulin heavy variable (III)-13-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5693]"}, {"versioned_ensembl_gene_id":"ENSG00000236429.1","gene_symbol":"GPM6BP2","gene_name":"glycoprotein M6B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38781]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480426","summary":null,"start":18741843,"end":18741986,"strand":-1,"description":"glycoprotein M6B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38781]"}, {"versioned_ensembl_gene_id":"ENSG00000270953.1","gene_symbol":"AC007938.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130507660,"end":130508282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259560.1","gene_symbol":"AC020687.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87432058,"end":87703852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272701.2","gene_symbol":"AC007938.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130486042,"end":130491033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196659.9","gene_symbol":"TTC30B","gene_name":"tetratricopeptide repeat domain 30B [Source:HGNC Symbol;Acc:HGNC:26425]","synonyms":"FLJ30990,fleer,IFT70B","biotype":"protein_coding","ncbi_id":"150737","summary":null,"start":177548998,"end":177553014,"strand":-1,"description":"tetratricopeptide repeat domain 30B [Source:HGNC Symbol;Acc:HGNC:26425]"}, {"versioned_ensembl_gene_id":"ENSG00000102468.10","gene_symbol":"HTR2A","gene_name":"5-hydroxytryptamine receptor 2A [Source:HGNC Symbol;Acc:HGNC:5293]","synonyms":"5-HT2A,HTR2","biotype":"protein_coding","ncbi_id":"3356","summary":"This gene encodes one of the receptors for serotonin, a neurotransmitter with many roles. Mutations in this gene are associated with susceptibility to schizophrenia and obsessive-compulsive disorder, and are also associated with response to the antidepressant citalopram in patients with major depressive disorder (MDD). MDD patients who also have a mutation in intron 2 of this gene show a significantly reduced response to citalopram as this antidepressant downregulates expression of this gene. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":46831550,"end":46897076,"strand":-1,"description":"5-hydroxytryptamine receptor 2A [Source:HGNC Symbol;Acc:HGNC:5293]"}, {"versioned_ensembl_gene_id":"ENSG00000197421.9","gene_symbol":"GGT3P","gene_name":"gamma-glutamyltransferase 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4252]","synonyms":"GGT3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"2679","summary":null,"start":18773665,"end":18843399,"strand":-1,"description":"gamma-glutamyltransferase 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:4252]"}, {"versioned_ensembl_gene_id":"ENSG00000278078.1","gene_symbol":"AC025279.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29380242,"end":29380345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185700.10","gene_symbol":"TTTY8B","gene_name":"testis-specific transcript, Y-linked 8B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37622]","synonyms":"NCRNA00217","biotype":"lincRNA","ncbi_id":"100101118","summary":null,"start":6470773,"end":6473630,"strand":-1,"description":"testis-specific transcript, Y-linked 8B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37622]"}, {"versioned_ensembl_gene_id":"ENSG00000198021.7","gene_symbol":"SPANXA1","gene_name":"sperm protein associated with the nucleus, X-linked, family member A1 [Source:HGNC Symbol;Acc:HGNC:11218]","synonyms":"SPANX,SPAN-Xb,SPAN-Xa,NAP-X,CT11.1","biotype":"protein_coding","ncbi_id":"30014","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene maps to chromosome X in a head-to-head orientation with SPANX family member A2, which appears to be a duplication of the A1 locus. The protein encoded by this gene targets to the nucleus where it associates with nuclear vacuoles and the redundant nuclear envelope. Based on its association with these poorly characterized regions of the sperm nucleus, this protein provides a biochemical marker to study unique structures in spermatazoa while attempting to further define its role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":141583674,"end":141585011,"strand":-1,"description":"sperm protein associated with the nucleus, X-linked, family member A1 [Source:HGNC Symbol;Acc:HGNC:11218]"}, {"versioned_ensembl_gene_id":"ENSG00000181873.12","gene_symbol":"IBA57","gene_name":"IBA57 homolog, iron-sulfur cluster assembly [Source:HGNC Symbol;Acc:HGNC:27302]","synonyms":"FLJ12734,C1orf69","biotype":"protein_coding","ncbi_id":"200205","summary":"The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide. [provided by RefSeq, Jul 2015]","start":228165815,"end":228182257,"strand":1,"description":"IBA57 homolog, iron-sulfur cluster assembly [Source:HGNC Symbol;Acc:HGNC:27302]"}, {"versioned_ensembl_gene_id":"ENSG00000224484.1","gene_symbol":"AC023141.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57776972,"end":57777521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237477.1","gene_symbol":"AC093911.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179273831,"end":179285707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280668.2","gene_symbol":"CCDC197","gene_name":"coiled-coil domain containing 197 [Source:NCBI gene;Acc:256369]","synonyms":"LINC00521,c14_5713,C14orf48,LINC00521,C14orf48","biotype":"lincRNA","ncbi_id":"256369","summary":null,"start":93997270,"end":94008863,"strand":1,"description":"coiled-coil domain containing 197 [Source:NCBI gene;Acc:256369]"}, {"versioned_ensembl_gene_id":"ENSG00000215088.3","gene_symbol":"RPS5P3","gene_name":"ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10427]","synonyms":"RPS5L","biotype":"processed_pseudogene","ncbi_id":"54022","summary":null,"start":33481580,"end":33482195,"strand":-1,"description":"ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10427]"}, {"versioned_ensembl_gene_id":"ENSG00000224323.2","gene_symbol":"DPRXP1","gene_name":"divergent-paired related homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503641","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":186488624,"end":186489083,"strand":-1,"description":"divergent-paired related homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32167]"}, {"versioned_ensembl_gene_id":"ENSG00000271064.1","gene_symbol":"AC027644.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66748838,"end":66749077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260653.5","gene_symbol":"AC237221.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57404771,"end":57416203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280061.1","gene_symbol":"AC011504.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30553956,"end":30558058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275613.1","gene_symbol":"AC243830.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36722583,"end":36726340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279112.1","gene_symbol":"BRI3BPP1","gene_name":"BRI3 binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51482]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100129976","summary":null,"start":21760226,"end":21762917,"strand":1,"description":"BRI3 binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51482]"}, {"versioned_ensembl_gene_id":"ENSG00000185903.9","gene_symbol":"AL590806.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131324398,"end":131325250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278143.1","gene_symbol":"NF1P7","gene_name":"neurofibromin 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34230]","synonyms":"NF1L7","biotype":"unprocessed_pseudogene","ncbi_id":"100158257","summary":null,"start":18899942,"end":18909673,"strand":-1,"description":"neurofibromin 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:34230]"}, {"versioned_ensembl_gene_id":"ENSG00000177854.7","gene_symbol":"TMEM187","gene_name":"transmembrane protein 187 [Source:HGNC Symbol;Acc:HGNC:13705]","synonyms":"ITBA1,DXS9878E,CXorf12","biotype":"protein_coding","ncbi_id":"8269","summary":"This gene consists of two exons and encodes a multi-pass membrane protein. An alternatively spliced transcript variant encoding the same protein has been found, but its biological validity is not determined. [provided by RefSeq, May 2010]","start":153972327,"end":153983195,"strand":1,"description":"transmembrane protein 187 [Source:HGNC Symbol;Acc:HGNC:13705]"}, {"versioned_ensembl_gene_id":"ENSG00000106028.10","gene_symbol":"SSBP1","gene_name":"single stranded DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11317]","synonyms":"mtSSB,SSBP","biotype":"protein_coding","ncbi_id":"6742","summary":"SSBP1 is a housekeeping gene involved in mitochondrial biogenesis (Tiranti et al., 1995 [PubMed 7789991]). It is also a subunit of a single-stranded DNA (ssDNA)-binding complex involved in the maintenance of genome stability (Huang et al., 2009) [PubMed 19683501].[supplied by OMIM, Feb 2010]","start":141738321,"end":141787922,"strand":1,"description":"single stranded DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11317]"}, {"versioned_ensembl_gene_id":"ENSG00000172613.7","gene_symbol":"RAD9A","gene_name":"RAD9 checkpoint clamp component A [Source:HGNC Symbol;Acc:HGNC:9827]","synonyms":"RAD9","biotype":"protein_coding","ncbi_id":"5883","summary":"This gene product is highly similar to Schizosaccharomyces pombe rad9, a cell cycle checkpoint protein required for cell cycle arrest and DNA damage repair. This protein possesses 3' to 5' exonuclease activity, which may contribute to its role in sensing and repairing DNA damage. It forms a checkpoint protein complex with RAD1 and HUS1. This complex is recruited by checkpoint protein RAD17 to the sites of DNA damage, which is thought to be important for triggering the checkpoint-signaling cascade. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":67317871,"end":67398410,"strand":1,"description":"RAD9 checkpoint clamp component A [Source:HGNC Symbol;Acc:HGNC:9827]"}, {"versioned_ensembl_gene_id":"ENSG00000224709.1","gene_symbol":"OR11M1P","gene_name":"olfactory receptor family 11 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15333]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"121270","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48627888,"end":48628782,"strand":1,"description":"olfactory receptor family 11 subfamily M member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15333]"}, {"versioned_ensembl_gene_id":"ENSG00000270838.1","gene_symbol":"AL121912.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22343693,"end":22343930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227270.1","gene_symbol":"AC009963.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":107903964,"end":107904241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204590.12","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30541377,"end":30557174,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000100299.17","gene_symbol":"ARSA","gene_name":"arylsulfatase A [Source:HGNC Symbol;Acc:HGNC:713]","synonyms":null,"biotype":"protein_coding","ncbi_id":"410","summary":"The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":50622754,"end":50628173,"strand":-1,"description":"arylsulfatase A [Source:HGNC Symbol;Acc:HGNC:713]"}, {"versioned_ensembl_gene_id":"ENSG00000087269.15","gene_symbol":"NOP14","gene_name":"NOP14 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:16821]","synonyms":"UTP2,RES4-25,NOL14,C4orf9","biotype":"protein_coding","ncbi_id":"8602","summary":"This gene encodes a protein that plays a role in pre-18s rRNA processing and small ribosomal subunit assembly. The encoded protein may be involved in the regulation of pancreatic cancer cell proliferation and migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":2937933,"end":2963385,"strand":-1,"description":"NOP14 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:16821]"}, {"versioned_ensembl_gene_id":"ENSG00000183318.11","gene_symbol":"SPDYE4","gene_name":"speedy/RINGO cell cycle regulator family member E4 [Source:HGNC Symbol;Acc:HGNC:35463]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388333","summary":null,"start":8753106,"end":8758559,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E4 [Source:HGNC Symbol;Acc:HGNC:35463]"}, {"versioned_ensembl_gene_id":"ENSG00000204576.11","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"CAT56,Em:AB023052.2,Em:AB014077.1","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30556886,"end":30563723,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000249673.6","gene_symbol":"NOP14-AS1","gene_name":"NOP14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20205]","synonyms":"C4orf10,RES4-24","biotype":"antisense_RNA","ncbi_id":"317648","summary":null,"start":2934899,"end":2961738,"strand":1,"description":"NOP14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20205]"}, {"versioned_ensembl_gene_id":"ENSG00000173540.12","gene_symbol":"GMPPB","gene_name":"GDP-mannose pyrophosphorylase B [Source:HGNC Symbol;Acc:HGNC:22932]","synonyms":"KIAA1851","biotype":"protein_coding","ncbi_id":"29925","summary":"This gene is thought to encode a GDP-mannose pyrophosphorylase. The encoded protein catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose, a reaction involved in the production of N-linked oligosaccharides. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2009]","start":49716844,"end":49723951,"strand":-1,"description":"GDP-mannose pyrophosphorylase B [Source:HGNC Symbol;Acc:HGNC:22932]"}, {"versioned_ensembl_gene_id":"ENSG00000280066.1","gene_symbol":"MTDHP4","gene_name":"metadherin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418834","summary":null,"start":21687036,"end":21687706,"strand":-1,"description":"metadherin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52360]"}, {"versioned_ensembl_gene_id":"ENSG00000150593.17","gene_symbol":"PDCD4","gene_name":"programmed cell death 4 [Source:HGNC Symbol;Acc:HGNC:8763]","synonyms":"H731","biotype":"protein_coding","ncbi_id":"27250","summary":"This gene is a tumor suppressor and encodes a protein that binds to the eukaryotic translation initiation factor 4A1 and inhibits its function by preventing RNA binding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":110871795,"end":110900006,"strand":1,"description":"programmed cell death 4 [Source:HGNC Symbol;Acc:HGNC:8763]"}, {"versioned_ensembl_gene_id":"ENSG00000237945.7","gene_symbol":"LINC00649","gene_name":"long intergenic non-protein coding RNA 649 [Source:HGNC Symbol;Acc:HGNC:44305]","synonyms":"TCONS_00028768","biotype":"antisense_RNA","ncbi_id":"100506334","summary":null,"start":33915534,"end":33977691,"strand":1,"description":"long intergenic non-protein coding RNA 649 [Source:HGNC Symbol;Acc:HGNC:44305]"}, {"versioned_ensembl_gene_id":"ENSG00000232971.2","gene_symbol":"AL591719.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108734256,"end":108734725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227261.1","gene_symbol":"YWHAZP7","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130640","summary":null,"start":64612632,"end":64613262,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39028]"}, {"versioned_ensembl_gene_id":"ENSG00000257607.1","gene_symbol":"AC073957.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1055360,"end":1059261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270589.1","gene_symbol":"AL158163.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110910596,"end":110912244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203497.2","gene_symbol":"PDCD4-AS1","gene_name":"PDCD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27425]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"282997","summary":null,"start":110869868,"end":110872233,"strand":-1,"description":"PDCD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27425]"}, {"versioned_ensembl_gene_id":"ENSG00000226213.1","gene_symbol":"UBQLN4P2","gene_name":"ubiquilin 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38662]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131393","summary":null,"start":152876820,"end":152877767,"strand":1,"description":"ubiquilin 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38662]"}, {"versioned_ensembl_gene_id":"ENSG00000278373.4","gene_symbol":"G6PC2","gene_name":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]","synonyms":"IGRP","biotype":"protein_coding","ncbi_id":"57818","summary":"This gene encodes an enzyme belonging to the glucose-6-phosphatase catalytic subunit family. These enzymes are part of a multicomponent integral membrane system that catalyzes the hydrolysis of glucose-6-phosphate, the terminal step in gluconeogenic and glycogenolytic pathways, allowing the release of glucose into the bloodstream. The family member encoded by this gene is found in pancreatic islets and does not exhibit phosphohydrolase activity, but it is a major target of cell-mediated autoimmunity in diabetes. Several alternatively spliced transcript variants of this gene have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":168918229,"end":168926984,"strand":1,"description":"glucose-6-phosphatase catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:28906]"}, {"versioned_ensembl_gene_id":"ENSG00000240095.1","gene_symbol":"AC055758.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145961755,"end":145963623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277504.1","gene_symbol":"AC010536.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87683945,"end":87684477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282872.1","gene_symbol":"C1orf232","gene_name":"chromosome 1 open reading frame 230 [Source:HGNC Symbol;Acc:HGNC:53426]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":26164161,"end":26168581,"strand":-1,"description":"chromosome 1 open reading frame 230 [Source:HGNC Symbol;Acc:HGNC:53426]"}, {"versioned_ensembl_gene_id":"ENSG00000213069.3","gene_symbol":"KRT8P40","gene_name":"keratin 8 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39874]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418728","summary":null,"start":177197985,"end":177198547,"strand":1,"description":"keratin 8 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:39874]"}, {"versioned_ensembl_gene_id":"ENSG00000229337.1","gene_symbol":"AC079305.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177155622,"end":177212662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103546.18","gene_symbol":"SLC6A2","gene_name":"solute carrier family 6 member 2 [Source:HGNC Symbol;Acc:HGNC:11048]","synonyms":"SLC6A5,NET1,NET,NAT1","biotype":"protein_coding","ncbi_id":"6530","summary":"This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]","start":55655604,"end":55706192,"strand":1,"description":"solute carrier family 6 member 2 [Source:HGNC Symbol;Acc:HGNC:11048]"}, {"versioned_ensembl_gene_id":"ENSG00000104231.10","gene_symbol":"ZFAND1","gene_name":"zinc finger AN1-type containing 1 [Source:HGNC Symbol;Acc:HGNC:25858]","synonyms":"FLJ14007","biotype":"protein_coding","ncbi_id":"79752","summary":null,"start":81701334,"end":81732903,"strand":-1,"description":"zinc finger AN1-type containing 1 [Source:HGNC Symbol;Acc:HGNC:25858]"}, {"versioned_ensembl_gene_id":"ENSG00000164695.4","gene_symbol":"CHMP4C","gene_name":"charged multivesicular body protein 4C [Source:HGNC Symbol;Acc:HGNC:30599]","synonyms":"VPS32C,Shax3,MGC22825","biotype":"protein_coding","ncbi_id":"92421","summary":"CHMP4C belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]","start":81732434,"end":81759515,"strand":1,"description":"charged multivesicular body protein 4C [Source:HGNC Symbol;Acc:HGNC:30599]"}, {"versioned_ensembl_gene_id":"ENSG00000278895.1","gene_symbol":"AC008507.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29915862,"end":29917830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214513.3","gene_symbol":"NOTO","gene_name":"notochord homeobox [Source:HGNC Symbol;Acc:HGNC:31839]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344022","summary":null,"start":73202258,"end":73212513,"strand":1,"description":"notochord homeobox [Source:HGNC Symbol;Acc:HGNC:31839]"}, {"versioned_ensembl_gene_id":"ENSG00000278000.1","gene_symbol":"AC139100.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":80161752,"end":80162413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177842.11","gene_symbol":"ZNF620","gene_name":"zinc finger protein 620 [Source:HGNC Symbol;Acc:HGNC:28742]","synonyms":"MGC50836","biotype":"protein_coding","ncbi_id":"253639","summary":null,"start":40505992,"end":40518736,"strand":1,"description":"zinc finger protein 620 [Source:HGNC Symbol;Acc:HGNC:28742]"}, {"versioned_ensembl_gene_id":"ENSG00000239696.3","gene_symbol":"AC092104.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7078302,"end":7079742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242731.3","gene_symbol":"FAM86LP","gene_name":"family with sequence similarity 86 member L, pseudogene [Source:HGNC Symbol;Acc:HGNC:44099]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"641924","summary":null,"start":6931684,"end":6939603,"strand":-1,"description":"family with sequence similarity 86 member L, pseudogene [Source:HGNC Symbol;Acc:HGNC:44099]"}, {"versioned_ensembl_gene_id":"ENSG00000164068.15","gene_symbol":"RNF123","gene_name":"ring finger protein 123 [Source:HGNC Symbol;Acc:HGNC:21148]","synonyms":"KPC1,FLJ12565","biotype":"protein_coding","ncbi_id":"63891","summary":"The protein encoded by this gene contains a C-terminal RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions, and an N-terminal SPRY domain. This protein displays E3 ubiquitin ligase activity toward the cyclin-dependent kinase inhibitor 1B which is also known as p27 or KIP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":49689499,"end":49721529,"strand":1,"description":"ring finger protein 123 [Source:HGNC Symbol;Acc:HGNC:21148]"}, {"versioned_ensembl_gene_id":"ENSG00000277870.5","gene_symbol":"FAM230A","gene_name":"family with sequence similarity 230 member A [Source:HGNC Symbol;Acc:HGNC:45045]","synonyms":"DGCR15","biotype":"protein_coding","ncbi_id":"653203","summary":null,"start":18422244,"end":18500594,"strand":1,"description":"family with sequence similarity 230 member A [Source:HGNC Symbol;Acc:HGNC:45045]"}, {"versioned_ensembl_gene_id":"ENSG00000241539.1","gene_symbol":"AC079804.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6924078,"end":6924513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217835.3","gene_symbol":"AL034397.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65956289,"end":65957196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182000.9","gene_symbol":"AC117395.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149984395,"end":149984797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224968.1","gene_symbol":"LINC01645","gene_name":"long intergenic non-protein coding RNA 1645 [Source:HGNC Symbol;Acc:HGNC:52432]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724661","summary":null,"start":177351586,"end":177366272,"strand":1,"description":"long intergenic non-protein coding RNA 1645 [Source:HGNC Symbol;Acc:HGNC:52432]"}, {"versioned_ensembl_gene_id":"ENSG00000135596.17","gene_symbol":"MICAL1","gene_name":"microtubule associated monooxygenase, calponin and LIM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20619]","synonyms":"NICAL,MICAL,FLJ21739,FLJ11937,DKFZp434B1517","biotype":"protein_coding","ncbi_id":"64780","summary":"This gene encodes an enzyme that oxidizes methionine residues on actin, thereby promoting depolymerization of actin filaments. This protein interacts with and regulates signalling by NEDD9/CAS-L (neural precursor cell expressed, developmentally down-regulated 9). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":109444062,"end":109465968,"strand":-1,"description":"microtubule associated monooxygenase, calponin and LIM domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20619]"}, {"versioned_ensembl_gene_id":"ENSG00000281127.1","gene_symbol":"AC226496.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68790295,"end":68790411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177685.16","gene_symbol":"CRACR2B","gene_name":"calcium release activated channel regulator 2B [Source:HGNC Symbol;Acc:HGNC:28703]","synonyms":"MGC45840,EFCAB4A","biotype":"protein_coding","ncbi_id":"283229","summary":null,"start":826144,"end":831991,"strand":1,"description":"calcium release activated channel regulator 2B [Source:HGNC Symbol;Acc:HGNC:28703]"}, {"versioned_ensembl_gene_id":"ENSG00000168539.3","gene_symbol":"CHRM1","gene_name":"cholinergic receptor muscarinic 1 [Source:HGNC Symbol;Acc:HGNC:1950]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1128","summary":"The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The muscarinic cholinergic receptor 1 is involved in mediation of vagally-induced bronchoconstriction and in the acid secretion of the gastrointestinal tract. The gene encoding this receptor is localized to 11q13. [provided by RefSeq, Jul 2008]","start":62908679,"end":62921807,"strand":-1,"description":"cholinergic receptor muscarinic 1 [Source:HGNC Symbol;Acc:HGNC:1950]"}, {"versioned_ensembl_gene_id":"ENSG00000253745.1","gene_symbol":"AC091163.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46922561,"end":46928832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224132.2","gene_symbol":"AC112715.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237257091,"end":237257676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124143.10","gene_symbol":"ARHGAP40","gene_name":"Rho GTPase activating protein 40 [Source:HGNC Symbol;Acc:HGNC:16226]","synonyms":"dJ1100H13.4,C20orf95","biotype":"protein_coding","ncbi_id":"343578","summary":null,"start":38601934,"end":38651035,"strand":1,"description":"Rho GTPase activating protein 40 [Source:HGNC Symbol;Acc:HGNC:16226]"}, {"versioned_ensembl_gene_id":"ENSG00000256306.1","gene_symbol":"AC007527.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":13526854,"end":13547582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185386.14","gene_symbol":"MAPK11","gene_name":"mitogen-activated protein kinase 11 [Source:HGNC Symbol;Acc:HGNC:6873]","synonyms":"SAPK2,PRKM11,p38Beta,p38-2","biotype":"protein_coding","ncbi_id":"5600","summary":"This gene encodes a member of a family of protein kinases that are involved in the integration of biochemical signals for a wide variety of cellular processes, including cell proliferation, differentiation, transcriptional regulation, and development. The encoded protein can be activated by proinflammatory cytokines and environmental stresses through phosphorylation by mitogen activated protein kinase kinases (MKKs). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":50263713,"end":50270767,"strand":-1,"description":"mitogen-activated protein kinase 11 [Source:HGNC Symbol;Acc:HGNC:6873]"}, {"versioned_ensembl_gene_id":"ENSG00000131069.19","gene_symbol":"ACSS2","gene_name":"acyl-CoA synthetase short chain family member 2 [Source:HGNC Symbol;Acc:HGNC:15814]","synonyms":"dJ1161H23.1,ACSA,ACS,AceCS,ACAS2","biotype":"protein_coding","ncbi_id":"55902","summary":"This gene encodes a cytosolic enzyme that catalyzes the activation of acetate for use in lipid synthesis and energy generation. The protein acts as a monomer and produces acetyl-CoA from acetate in a reaction that requires ATP. Expression of this gene is regulated by sterol regulatory element-binding proteins, transcription factors that activate genes required for the synthesis of cholesterol and unsaturated fatty acids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]","start":34872146,"end":34927962,"strand":1,"description":"acyl-CoA synthetase short chain family member 2 [Source:HGNC Symbol;Acc:HGNC:15814]"}, {"versioned_ensembl_gene_id":"ENSG00000163364.9","gene_symbol":"LINC01116","gene_name":"long intergenic non-protein coding RNA 1116 [Source:HGNC Symbol;Acc:HGNC:49259]","synonyms":"TALNEC2","biotype":"lincRNA","ncbi_id":"375295","summary":null,"start":176629589,"end":176637931,"strand":-1,"description":"long intergenic non-protein coding RNA 1116 [Source:HGNC Symbol;Acc:HGNC:49259]"}, {"versioned_ensembl_gene_id":"ENSG00000275838.5","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54794614,"end":54811438,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000133083.14","gene_symbol":"DCLK1","gene_name":"doublecortin like kinase 1 [Source:HGNC Symbol;Acc:HGNC:2700]","synonyms":"KIAA0369,DCLK,DCDC3A,DCAMKL1","biotype":"protein_coding","ncbi_id":"9201","summary":"This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. The encoded protein is involved in several different cellular processes, including neuronal migration, retrograde transport, neuronal apoptosis and neurogenesis. This gene is up-regulated by brain-derived neurotrophic factor and associated with memory and general cognitive abilities. Multiple transcript variants generated by two alternative promoter usage and alternative splicing have been reported, but the full-length nature and biological validity of some variants have not been defined. These variants encode different isoforms, which are differentially expressed and have different kinase activities.[provided by RefSeq, Sep 2010]","start":35768652,"end":36131306,"strand":-1,"description":"doublecortin like kinase 1 [Source:HGNC Symbol;Acc:HGNC:2700]"}, {"versioned_ensembl_gene_id":"ENSG00000236413.2","gene_symbol":"AL662874.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91422309,"end":91422538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000014824.13","gene_symbol":"SLC30A9","gene_name":"solute carrier family 30 member 9 [Source:HGNC Symbol;Acc:HGNC:1329]","synonyms":"ZNT9,HUEL,GAC63,C4orf1","biotype":"protein_coding","ncbi_id":"10463","summary":null,"start":41990472,"end":42090457,"strand":1,"description":"solute carrier family 30 member 9 [Source:HGNC Symbol;Acc:HGNC:1329]"}, {"versioned_ensembl_gene_id":"ENSG00000223481.9","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"D6S217E,RING11,ABCB3,PSF2","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32799958,"end":32816755,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000227642.9","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32207600,"end":32217484,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000137273.3","gene_symbol":"FOXF2","gene_name":"forkhead box F2 [Source:HGNC Symbol;Acc:HGNC:3810]","synonyms":"FREAC2,FKHL6","biotype":"protein_coding","ncbi_id":"2295","summary":"FOXF2 encodes forkhead box F2, one of many human homologues of the Drosophila melanogaster transcription factor forkhead. FOXF2 is expressed in lung and placenta, and has been shown to transcriptionally activate several lung-specific genes. [provided by RefSeq, Jul 2008]","start":1389834,"end":1395597,"strand":1,"description":"forkhead box F2 [Source:HGNC Symbol;Acc:HGNC:3810]"}, {"versioned_ensembl_gene_id":"ENSG00000162994.15","gene_symbol":"CLHC1","gene_name":"clathrin heavy chain linker domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26453]","synonyms":"FLJ31438,C2orf63","biotype":"protein_coding","ncbi_id":"130162","summary":null,"start":55174791,"end":55232563,"strand":-1,"description":"clathrin heavy chain linker domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26453]"}, {"versioned_ensembl_gene_id":"ENSG00000228659.1","gene_symbol":"LINC01201","gene_name":"long intergenic non-protein coding RNA 1201 [Source:HGNC Symbol;Acc:HGNC:49632]","synonyms":"TCONS_00017091","biotype":"antisense_RNA","ncbi_id":"104266960","summary":null,"start":130981590,"end":131058146,"strand":-1,"description":"long intergenic non-protein coding RNA 1201 [Source:HGNC Symbol;Acc:HGNC:49632]"}, {"versioned_ensembl_gene_id":"ENSG00000135931.17","gene_symbol":"ARMC9","gene_name":"armadillo repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:20730]","synonyms":"KU-MEL-1,KIAA1868,FLJ12584,ARM","biotype":"protein_coding","ncbi_id":"80210","summary":null,"start":231198546,"end":231374837,"strand":1,"description":"armadillo repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:20730]"}, {"versioned_ensembl_gene_id":"ENSG00000275340.1","gene_symbol":"FGD5P1","gene_name":"FYVE, RhoGEF and PH domain containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44498]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132526","summary":null,"start":13933056,"end":13937477,"strand":1,"description":"FYVE, RhoGEF and PH domain containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44498]"}, {"versioned_ensembl_gene_id":"ENSG00000083937.8","gene_symbol":"CHMP2B","gene_name":"charged multivesicular body protein 2B [Source:HGNC Symbol;Acc:HGNC:24537]","synonyms":"VPS2B,DKFZP564O123,CHMP2.5","biotype":"protein_coding","ncbi_id":"25978","summary":"This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration. [provided by RefSeq, Jul 2008]","start":87227271,"end":87255548,"strand":1,"description":"charged multivesicular body protein 2B [Source:HGNC Symbol;Acc:HGNC:24537]"}, {"versioned_ensembl_gene_id":"ENSG00000261774.1","gene_symbol":"AC009075.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72278268,"end":72278568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163884.3","gene_symbol":"KLF15","gene_name":"Kruppel like factor 15 [Source:HGNC Symbol;Acc:HGNC:14536]","synonyms":"KKLF","biotype":"protein_coding","ncbi_id":"28999","summary":null,"start":126342635,"end":126357442,"strand":-1,"description":"Kruppel like factor 15 [Source:HGNC Symbol;Acc:HGNC:14536]"}, {"versioned_ensembl_gene_id":"ENSG00000092295.11","gene_symbol":"TGM1","gene_name":"transglutaminase 1 [Source:HGNC Symbol;Acc:HGNC:11777]","synonyms":"TGK,TGASE,LI1,LI,ICR2","biotype":"protein_coding","ncbi_id":"7051","summary":"The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE). [provided by RefSeq, Jul 2008]","start":24249114,"end":24264432,"strand":-1,"description":"transglutaminase 1 [Source:HGNC Symbol;Acc:HGNC:11777]"}, {"versioned_ensembl_gene_id":"ENSG00000130522.5","gene_symbol":"JUND","gene_name":"JunD proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6206]","synonyms":"AP-1","biotype":"protein_coding","ncbi_id":"3727","summary":"The protein encoded by this intronless gene is a member of the JUN family, and a functional component of the AP1 transcription factor complex. This protein has been proposed to protect cells from p53-dependent senescence and apoptosis. Alternative translation initiation site usage results in the production of different isoforms (PMID:12105216). [provided by RefSeq, Nov 2013]","start":18279760,"end":18281622,"strand":-1,"description":"JunD proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6206]"}, {"versioned_ensembl_gene_id":"ENSG00000282818.1","gene_symbol":"IGHD2-15","gene_name":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]","synonyms":"D2,IGHD215","biotype":"IG_D_gene","ncbi_id":"28503","summary":null,"start":105898728,"end":105898758,"strand":-1,"description":"immunoglobulin heavy diversity 2-15 [Source:HGNC Symbol;Acc:HGNC:5489]"}, {"versioned_ensembl_gene_id":"ENSG00000228338.1","gene_symbol":"LINC01784","gene_name":"long intergenic non-protein coding RNA 1784 [Source:HGNC Symbol;Acc:HGNC:52574]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376745","summary":null,"start":12822686,"end":12823159,"strand":-1,"description":"long intergenic non-protein coding RNA 1784 [Source:HGNC Symbol;Acc:HGNC:52574]"}, {"versioned_ensembl_gene_id":"ENSG00000227581.2","gene_symbol":"AL121877.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90039213,"end":90039834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230514.11","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32257394,"end":32260750,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000282736.1","gene_symbol":"IGHD1-14","gene_name":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]","synonyms":"DM2,IGHD114","biotype":"IG_D_gene","ncbi_id":"28508","summary":null,"start":105901409,"end":105901425,"strand":-1,"description":"immunoglobulin heavy diversity 1-14 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5483]"}, {"versioned_ensembl_gene_id":"ENSG00000185900.9","gene_symbol":"POMK","gene_name":"protein-O-mannose kinase [Source:HGNC Symbol;Acc:HGNC:26267]","synonyms":"SgK196,FLJ23356","biotype":"protein_coding","ncbi_id":"84197","summary":"This gene encodes a protein that may be involved in the presentation of the laminin-binding O-linked carbohydrate chain of alpha-dystroglycan (a-DG), which forms transmembrane linkages between the extracellular matrix and the exoskeleton. Some pathogens use this O-linked carbohydrate unit for host entry. Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype. Mice lacking this gene contain misplaced neurons (heterotopia) in some regions of the brain, possibly from defects in neuronal migration. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":43093506,"end":43123434,"strand":1,"description":"protein-O-mannose kinase [Source:HGNC Symbol;Acc:HGNC:26267]"}, {"versioned_ensembl_gene_id":"ENSG00000274580.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54882451,"end":54899533,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000226081.2","gene_symbol":"USP12PX","gene_name":"ubiquitin specific peptidase 12 pseudogene, X-linked [Source:HGNC Symbol;Acc:HGNC:21410]","synonyms":"USP12P2","biotype":"processed_pseudogene","ncbi_id":"254700","summary":null,"start":90112650,"end":90113706,"strand":1,"description":"ubiquitin specific peptidase 12 pseudogene, X-linked [Source:HGNC Symbol;Acc:HGNC:21410]"}, {"versioned_ensembl_gene_id":"ENSG00000239810.3","gene_symbol":"PRAMEF11","gene_name":"PRAME family member 11 [Source:HGNC Symbol;Acc:HGNC:14086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440560","summary":null,"start":12824605,"end":12831410,"strand":-1,"description":"PRAME family member 11 [Source:HGNC Symbol;Acc:HGNC:14086]"}, {"versioned_ensembl_gene_id":"ENSG00000282042.1","gene_symbol":"IGHD6-13","gene_name":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]","synonyms":"IGHD613,DN1","biotype":"IG_D_gene","ncbi_id":"28487","summary":null,"start":105901913,"end":105901933,"strand":-1,"description":"immunoglobulin heavy diversity 6-13 [Source:HGNC Symbol;Acc:HGNC:5514]"}, {"versioned_ensembl_gene_id":"ENSG00000223890.1","gene_symbol":"AC008171.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205253304,"end":205253503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213057.5","gene_symbol":"C1orf220","gene_name":"chromosome 1 open reading frame 220 [Source:HGNC Symbol;Acc:HGNC:33805]","synonyms":"FLJ35530","biotype":"lincRNA","ncbi_id":"400798","summary":null,"start":178542752,"end":178548889,"strand":1,"description":"chromosome 1 open reading frame 220 [Source:HGNC Symbol;Acc:HGNC:33805]"}, {"versioned_ensembl_gene_id":"ENSG00000280166.1","gene_symbol":"AC016542.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":72730557,"end":72731175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280809.2","gene_symbol":"LINC00836","gene_name":"long intergenic non-protein coding RNA 836 [Source:HGNC Symbol;Acc:HGNC:44915]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929052","summary":null,"start":25651712,"end":25732935,"strand":1,"description":"long intergenic non-protein coding RNA 836 [Source:HGNC Symbol;Acc:HGNC:44915]"}, {"versioned_ensembl_gene_id":"ENSG00000240021.9","gene_symbol":"TEX35","gene_name":"testis expressed 35 [Source:HGNC Symbol;Acc:HGNC:25366]","synonyms":"TSC24,DKFZP564J047,C1orf49","biotype":"protein_coding","ncbi_id":"84066","summary":null,"start":178513077,"end":178548602,"strand":1,"description":"testis expressed 35 [Source:HGNC Symbol;Acc:HGNC:25366]"}, {"versioned_ensembl_gene_id":"ENSG00000275658.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54746977,"end":54761521,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000231103.2","gene_symbol":"PRAMEF30P","gene_name":"PRAME family member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:51892]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441870","summary":null,"start":12838125,"end":12841357,"strand":-1,"description":"PRAME family member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:51892]"}, {"versioned_ensembl_gene_id":"ENSG00000002726.20","gene_symbol":"AOC1","gene_name":"amine oxidase, copper containing 1 [Source:HGNC Symbol;Acc:HGNC:80]","synonyms":"DAO,ABP1","biotype":"protein_coding","ncbi_id":"26","summary":"This gene encodes a metal-binding membrane glycoprotein that oxidatively deaminates putrescine, histamine, and related compounds. The encoded protein is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013]","start":150824627,"end":150861504,"strand":1,"description":"amine oxidase, copper containing 1 [Source:HGNC Symbol;Acc:HGNC:80]"}, {"versioned_ensembl_gene_id":"ENSG00000271563.1","gene_symbol":"HIRAP1","gene_name":"histone cell cycle regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422545","summary":null,"start":25691537,"end":25692323,"strand":1,"description":"histone cell cycle regulator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44916]"}, {"versioned_ensembl_gene_id":"ENSG00000226304.1","gene_symbol":"AL358612.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25924448,"end":25933710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110888.17","gene_symbol":"CAPRIN2","gene_name":"caprin family member 2 [Source:HGNC Symbol;Acc:HGNC:21259]","synonyms":"RNG140,FLJ22569,FLJ11391,EEG1,caprin-2,C1QDC1","biotype":"protein_coding","ncbi_id":"65981","summary":"The protein encoded by this gene may regulate the transport of mRNA. It may play a role in the differentiation of erythroblasts. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":30709552,"end":30754951,"strand":-1,"description":"caprin family member 2 [Source:HGNC Symbol;Acc:HGNC:21259]"}, {"versioned_ensembl_gene_id":"ENSG00000169758.12","gene_symbol":"TMEM266","gene_name":"transmembrane protein 266 [Source:HGNC Symbol;Acc:HGNC:26763]","synonyms":"FLJ38190,C15orf27","biotype":"protein_coding","ncbi_id":"123591","summary":null,"start":76059837,"end":76229121,"strand":1,"description":"transmembrane protein 266 [Source:HGNC Symbol;Acc:HGNC:26763]"}, {"versioned_ensembl_gene_id":"ENSG00000137801.10","gene_symbol":"THBS1","gene_name":"thrombospondin 1 [Source:HGNC Symbol;Acc:HGNC:11785]","synonyms":"TSP1,TSP-1,TSP,THBS-1,THBS","biotype":"protein_coding","ncbi_id":"7057","summary":"The protein encoded by this gene is a subunit of a disulfide-linked homotrimeric protein. This protein is an adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions. This protein can bind to fibrinogen, fibronectin, laminin, type V collagen and integrins alpha-V/beta-1. This protein has been shown to play roles in platelet aggregation, angiogenesis, and tumorigenesis. [provided by RefSeq, Jul 2008]","start":39581079,"end":39599466,"strand":1,"description":"thrombospondin 1 [Source:HGNC Symbol;Acc:HGNC:11785]"}, {"versioned_ensembl_gene_id":"ENSG00000009307.15","gene_symbol":"CSDE1","gene_name":"cold shock domain containing E1 [Source:HGNC Symbol;Acc:HGNC:29905]","synonyms":"UNR,D1S155E","biotype":"protein_coding","ncbi_id":"7812","summary":null,"start":114716913,"end":114758676,"strand":-1,"description":"cold shock domain containing E1 [Source:HGNC Symbol;Acc:HGNC:29905]"}, {"versioned_ensembl_gene_id":"ENSG00000220575.7","gene_symbol":"HTR5A-AS1","gene_name":"HTR5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48956]","synonyms":"HTR5AOS","biotype":"antisense_RNA","ncbi_id":"100128264","summary":null,"start":155067067,"end":155071557,"strand":-1,"description":"HTR5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48956]"}, {"versioned_ensembl_gene_id":"ENSG00000091157.13","gene_symbol":"WDR7","gene_name":"WD repeat domain 7 [Source:HGNC Symbol;Acc:HGNC:13490]","synonyms":"TRAG,KIAA0541","biotype":"protein_coding","ncbi_id":"23335","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) that may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. The encoded protein forms the beta subunit of rabconnectin-3 and binds directly with Rab3A GDP/GTP exchange protein and indirectly with Rab3A GDP/GTP activating protein; these proteins are regulators of Rab3 small G protein family members involved in control of the calcium-dependant exocytosis of neurotransmitters. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":56651343,"end":57036606,"strand":1,"description":"WD repeat domain 7 [Source:HGNC Symbol;Acc:HGNC:13490]"}, {"versioned_ensembl_gene_id":"ENSG00000205596.4","gene_symbol":"AC068533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66070904,"end":66071318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072840.12","gene_symbol":"EVC","gene_name":"EvC ciliary complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:3497]","synonyms":"DWF-1","biotype":"protein_coding","ncbi_id":"2121","summary":"This gene encodes a protein containing a leucine zipper and a transmembrane domain. This gene has been implicated in both Ellis-van Creveld syndrome (EvC) and Weyers acrodental dysostosis. [provided by RefSeq, Jul 2008]","start":5711197,"end":5814305,"strand":1,"description":"EvC ciliary complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:3497]"}, {"versioned_ensembl_gene_id":"ENSG00000255447.1","gene_symbol":"AC044839.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45813219,"end":45825258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198026.7","gene_symbol":"ZNF335","gene_name":"zinc finger protein 335 [Source:HGNC Symbol;Acc:HGNC:15807]","synonyms":"NIF-1,bA465L10.2","biotype":"protein_coding","ncbi_id":"63925","summary":"The protein encoded by this gene enhances transcriptional activation by ligand-bound nuclear hormone receptors. However, it does this not by direct interaction with the receptor, but by direct interaction with the nuclear hormone receptor transcriptional coactivator NRC. The encoded protein may function by altering local chromatin structure. [provided by RefSeq, Jul 2008]","start":45948653,"end":45972172,"strand":-1,"description":"zinc finger protein 335 [Source:HGNC Symbol;Acc:HGNC:15807]"}, {"versioned_ensembl_gene_id":"ENSG00000262712.1","gene_symbol":"AC012676.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4335870,"end":4337818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168140.4","gene_symbol":"VASN","gene_name":"vasorin [Source:HGNC Symbol;Acc:HGNC:18517]","synonyms":"SLITL2","biotype":"protein_coding","ncbi_id":"114990","summary":null,"start":4371848,"end":4383528,"strand":1,"description":"vasorin [Source:HGNC Symbol;Acc:HGNC:18517]"}, {"versioned_ensembl_gene_id":"ENSG00000271096.1","gene_symbol":"SUMO2P14","gene_name":"SUMO2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480264","summary":null,"start":24589115,"end":24589407,"strand":-1,"description":"SUMO2 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49352]"}, {"versioned_ensembl_gene_id":"ENSG00000262156.4","gene_symbol":"APOBEC3A","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A [Source:HGNC Symbol;Acc:HGNC:17343]","synonyms":"PHRBN,ARP3","biotype":"protein_coding","ncbi_id":"200315","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. The protein encoded by this gene lacks the zinc binding activity of other family members. The protein plays a role in immunity, by restricting transmission of foreign DNA such as viruses. One mechanism of foreign DNA restriction is deamination of foreign double-stranded DNA cytidines to uridines, which leads to DNA degradation. However, other mechanisms are also thought to be involved, as anti-viral effect is not dependent on deaminase activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]","start":38952742,"end":38962839,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A [Source:HGNC Symbol;Acc:HGNC:17343]"}, {"versioned_ensembl_gene_id":"ENSG00000271330.1","gene_symbol":"AC005084.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24674309,"end":24674612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111602.11","gene_symbol":"TIMELESS","gene_name":"timeless circadian clock [Source:HGNC Symbol;Acc:HGNC:11813]","synonyms":"TIM1,TIM,hTIM","biotype":"protein_coding","ncbi_id":"8914","summary":"The protein encoded by this gene is highly conserved and is involved in cell survival after damage or stress, increase in DNA polymerase epsilon activity, maintenance of telomere length, and epithelial cell morphogenesis. The encoded protein also plays a role in the circadian rhythm autoregulatory loop, interacting with the PERIOD genes (PER1, PER2, and PER3) and others to downregulate activation of PER1 by CLOCK/ARNTL. Changes in this gene or its expression may promote prostate cancer, lung cancer, breast cancer, and mental disorders. [provided by RefSeq, Feb 2014]","start":56416373,"end":56449403,"strand":-1,"description":"timeless circadian clock [Source:HGNC Symbol;Acc:HGNC:11813]"}, {"versioned_ensembl_gene_id":"ENSG00000141424.12","gene_symbol":"SLC39A6","gene_name":"solute carrier family 39 member 6 [Source:HGNC Symbol;Acc:HGNC:18607]","synonyms":"LIV-1","biotype":"protein_coding","ncbi_id":"25800","summary":"Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A6 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]","start":36108532,"end":36129385,"strand":-1,"description":"solute carrier family 39 member 6 [Source:HGNC Symbol;Acc:HGNC:18607]"}, {"versioned_ensembl_gene_id":"ENSG00000103426.12","gene_symbol":"CORO7-PAM16","gene_name":"CORO7-PAM16 readthrough [Source:HGNC Symbol;Acc:HGNC:44424]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529144","summary":"This locus represents naturally occurring read-through transcription between the neighboring CORO7 (coronin 7) and PAM16 (presequence translocase-associated motor 16) genes on chromosome 16. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jan 2011]","start":4340251,"end":4420494,"strand":-1,"description":"CORO7-PAM16 readthrough [Source:HGNC Symbol;Acc:HGNC:44424]"}, {"versioned_ensembl_gene_id":"ENSG00000273753.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRZ,KIR15,KIR2DL6,KIRY","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54763492,"end":54775840,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000223391.2","gene_symbol":"AC006210.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27517771,"end":27517881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238247.2","gene_symbol":"AC006210.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27517884,"end":27519759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262213.1","gene_symbol":"AC144836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1241939,"end":1254000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236144.6","gene_symbol":"TMEM147-AS1","gene_name":"TMEM147 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51273]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506469","summary":null,"start":35540738,"end":35546029,"strand":-1,"description":"TMEM147 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51273]"}, {"versioned_ensembl_gene_id":"ENSG00000205899.3","gene_symbol":"BHLHA9","gene_name":"basic helix-loop-helix family member a9 [Source:HGNC Symbol;Acc:HGNC:35126]","synonyms":"BHLHF42,bHLHa9","biotype":"protein_coding","ncbi_id":"727857","summary":"This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3). [provided by RefSeq, Mar 2015]","start":1270559,"end":1271460,"strand":1,"description":"basic helix-loop-helix family member a9 [Source:HGNC Symbol;Acc:HGNC:35126]"}, {"versioned_ensembl_gene_id":"ENSG00000268949.1","gene_symbol":"MRPS17P1","gene_name":"mitochondrial ribosomal protein S17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359803","summary":null,"start":44988705,"end":44991834,"strand":-1,"description":"mitochondrial ribosomal protein S17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29734]"}, {"versioned_ensembl_gene_id":"ENSG00000244358.1","gene_symbol":"AC055758.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145939912,"end":145961536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154764.5","gene_symbol":"WNT7A","gene_name":"Wnt family member 7A [Source:HGNC Symbol;Acc:HGNC:12786]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7476","summary":"This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes. [provided by RefSeq, Jul 2008]","start":13816258,"end":13880121,"strand":-1,"description":"Wnt family member 7A [Source:HGNC Symbol;Acc:HGNC:12786]"}, {"versioned_ensembl_gene_id":"ENSG00000105679.8","gene_symbol":"GAPDHS","gene_name":"glyceraldehyde-3-phosphate dehydrogenase, spermatogenic [Source:HGNC Symbol;Acc:HGNC:24864]","synonyms":"GAPDS,GAPDH-2,GAPD2","biotype":"protein_coding","ncbi_id":"26330","summary":"This gene encodes a protein belonging to the glyceraldehyde-3-phosphate dehydrogenase family of enzymes that play an important role in carbohydrate metabolism. Like its somatic cell counterpart, this sperm-specific enzyme functions in a nicotinamide adenine dinucleotide-dependent manner to remove hydrogen and add phosphate to glyceraldehyde 3-phosphate to form 1,3-diphosphoglycerate. During spermiogenesis, this enzyme may play an important role in regulating the switch between different energy-producing pathways, and it is required for sperm motility and male fertility. [provided by RefSeq, Jul 2008]","start":35533412,"end":35545316,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase, spermatogenic [Source:HGNC Symbol;Acc:HGNC:24864]"}, {"versioned_ensembl_gene_id":"ENSG00000137100.15","gene_symbol":"DCTN3","gene_name":"dynactin subunit 3 [Source:HGNC Symbol;Acc:HGNC:2713]","synonyms":"DCTN-22","biotype":"protein_coding","ncbi_id":"11258","summary":"This gene encodes the smallest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, cytokinesis, chromosome movement, nuclear positioning, and axonogenesis. This subunit, like most other dynactin subunits, exists only as a part of the dynactin complex. It is primarily an alpha-helical protein with very little coiled coil, and binds directly to the largest subunit (p150) of dynactin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":34613545,"end":34620523,"strand":-1,"description":"dynactin subunit 3 [Source:HGNC Symbol;Acc:HGNC:2713]"}, {"versioned_ensembl_gene_id":"ENSG00000096093.15","gene_symbol":"EFHC1","gene_name":"EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16406]","synonyms":"FLJ10466,EJM1,EJM","biotype":"protein_coding","ncbi_id":"114327","summary":"This gene encodes an EF-hand-containing calcium binding protein. The encoded protein likely plays a role in calcium homeostasis. Mutations in this gene have been associated with susceptibility to juvenile myoclonic epilepsy and juvenile absence epilepsy. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]","start":52362123,"end":52529886,"strand":1,"description":"EF-hand domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16406]"}, {"versioned_ensembl_gene_id":"ENSG00000278621.1","gene_symbol":"AC037198.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39588357,"end":39588882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276107.1","gene_symbol":"AC037198.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39586561,"end":39587293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276387.4","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"CD158H,EB6ActII,EB6ActI,EB6ActI,CD158H,EB6ActII","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54778277,"end":54792578,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000259279.1","gene_symbol":"AC037198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39593580,"end":39594231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179172.9","gene_symbol":"HNRNPCL1","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:HGNC:29295]","synonyms":"HNRPCL1","biotype":"protein_coding","ncbi_id":"343069","summary":null,"start":12847408,"end":12848725,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:HGNC:29295]"}, {"versioned_ensembl_gene_id":"ENSG00000214612.3","gene_symbol":"RPS19P1","gene_name":"ribosomal protein S19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16534]","synonyms":"bA189K21.7","biotype":"processed_pseudogene","ncbi_id":"85486","summary":null,"start":18504633,"end":18505066,"strand":1,"description":"ribosomal protein S19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16534]"}, {"versioned_ensembl_gene_id":"ENSG00000163354.14","gene_symbol":"DCST2","gene_name":"DC-STAMP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26562]","synonyms":"FLJ32934","biotype":"protein_coding","ncbi_id":"127579","summary":null,"start":155018520,"end":155033781,"strand":-1,"description":"DC-STAMP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26562]"}, {"versioned_ensembl_gene_id":"ENSG00000178209.14","gene_symbol":"PLEC","gene_name":"plectin [Source:HGNC Symbol;Acc:HGNC:9069]","synonyms":"PLTN,PLEC1,PCN,EBS1","biotype":"protein_coding","ncbi_id":"5339","summary":"Plectin is a prominent member of an important family of structurally and in part functionally related proteins, termed plakins or cytolinkers, that are capable of interlinking different elements of the cytoskeleton. Plakins, with their multi-domain structure and enormous size, not only play crucial roles in maintaining cell and tissue integrity and orchestrating dynamic changes in cytoarchitecture and cell shape, but also serve as scaffolding platforms for the assembly, positioning, and regulation of signaling complexes (reviewed in PMID: 9701547, 11854008, and 17499243). Plectin is expressed as several protein isoforms in a wide range of cell types and tissues from a single gene located on chromosome 8 in humans (PMID: 8633055, 8698233). Until 2010, this locus was named plectin 1 (symbol PLEC1 in human; Plec1 in mouse and rat) and the gene product had been referred to as \"hemidesmosomal protein 1\" or \"plectin 1, intermediate filament binding 500kDa\". These names were superseded by plectin. The plectin gene locus in mouse on chromosome 15 has been analyzed in detail (PMID: 10556294, 14559777), revealing a genomic exon-intron organization with well over 40 exons spanning over 62 kb and an unusual 5' transcript complexity of plectin isoforms. Eleven exons (1-1j) have been identified that alternatively splice directly into a common exon 2 which is the first exon to encode plectin's highly conserved actin binding domain (ABD). Three additional exons (-1, 0a, and 0) splice into an alternative first coding exon (1c), and two additional exons (2alpha and 3alpha) are optionally spliced within the exons encoding the acting binding domain (exons 2-8). Analysis of the human locus has identified eight of the eleven alternative 5' exons found in mouse and rat (PMID: 14672974); exons 1i, 1j and 1h have not been confirmed in human. Furthermore, isoforms lacking the central rod domain encoded by exon 31 have been detected in mouse (PMID:10556294), rat (PMID: 9177781), and human (PMID: 11441066, 10780662, 20052759). The short alternative amino-terminal sequences encoded by the different first exons direct the targeting of the various isoforms to distinct subcellular locations (PMID: 14559777). As the expression of specific plectin isoforms was found to be dependent on cell type (tissue) and stage of development (PMID: 10556294, 12542521, 17389230) it appears that each cell type (tissue) contains a unique set (proportion and composition) of plectin isoforms, as if custom-made for specific requirements of the particular cells. Concordantly, individual isoforms were found to carry out distinct and specific functions (PMID: 14559777, 12542521, 18541706). In 1996, a number of groups reported that patients suffering from epidermolysis bullosa simplex with muscular dystrophy (EBS-MD) lacked plectin expression in skin and muscle tissues due to defects in the plectin gene (PMID: 8698233, 8941634, 8636409, 8894687, 8696340). Two other subtypes of plectin-related EBS have been described: EBS-pyloric atresia (PA) and EBS-Ogna. For reviews of plectin-related diseases see PMID: 15810881, 19945614. Mutations in the plectin gene related to human diseases should be named based on the position in NM_000445 (variant 1, isoform 1c), unless the mutation is located within one of the other alternative first exons, in which case the position in the respective Reference Sequence should be used. [provided by RefSeq, Aug 2011]","start":143915147,"end":143976734,"strand":-1,"description":"plectin [Source:HGNC Symbol;Acc:HGNC:9069]"}, {"versioned_ensembl_gene_id":"ENSG00000248848.1","gene_symbol":"PPBPP2","gene_name":"pro-platelet basic protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16981]","synonyms":"SPBPBP,PPBPL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10895","summary":null,"start":74054038,"end":74055399,"strand":-1,"description":"pro-platelet basic protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16981]"}, {"versioned_ensembl_gene_id":"ENSG00000152583.12","gene_symbol":"SPARCL1","gene_name":"SPARC like 1 [Source:HGNC Symbol;Acc:HGNC:11220]","synonyms":"MAST9","biotype":"protein_coding","ncbi_id":"8404","summary":null,"start":87473335,"end":87531061,"strand":-1,"description":"SPARC like 1 [Source:HGNC Symbol;Acc:HGNC:11220]"}, {"versioned_ensembl_gene_id":"ENSG00000231748.1","gene_symbol":"AL596223.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69265342,"end":69268148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261199.1","gene_symbol":"UBE2FP2","gene_name":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44536]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060189","summary":null,"start":63180610,"end":63181071,"strand":-1,"description":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44536]"}, {"versioned_ensembl_gene_id":"ENSG00000230411.1","gene_symbol":"OR3D1P","gene_name":"olfactory receptor family 3 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:25339]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"504175","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247666887,"end":247667841,"strand":1,"description":"olfactory receptor family 3 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:25339]"}, {"versioned_ensembl_gene_id":"ENSG00000153230.4","gene_symbol":"OR14K1","gene_name":"olfactory receptor family 14 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:15025]","synonyms":"OR5AY1","biotype":"protein_coding","ncbi_id":"343170","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247738615,"end":247739559,"strand":1,"description":"olfactory receptor family 14 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:15025]"}, {"versioned_ensembl_gene_id":"ENSG00000125510.15","gene_symbol":"OPRL1","gene_name":"opioid related nociceptin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8155]","synonyms":"KOR-3,ORL1,OOR,NOPr,NOCIR","biotype":"protein_coding","ncbi_id":"4987","summary":"The protein encoded by this gene is a member of the 7 transmembrane-spanning G protein-coupled receptor family, and functions as a receptor for the endogenous, opioid-related neuropeptide, nociceptin/orphanin FQ. This receptor-ligand system modulates a variety of biological functions and neurobehavior, including stress responses and anxiety behavior, learning and memory, locomotor activity, and inflammatory and immune responses. A promoter region between this gene and the 5'-adjacent RGS19 (regulator of G-protein signaling 19) gene on the opposite strand functions bi-directionally as a core-promoter for both genes, suggesting co-operative transcriptional regulation of these two functionally related genes. Alternatively spliced transcript variants have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]","start":64080173,"end":64100643,"strand":1,"description":"opioid related nociceptin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8155]"}, {"versioned_ensembl_gene_id":"ENSG00000127463.14","gene_symbol":"EMC1","gene_name":"ER membrane protein complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28957]","synonyms":"KIAA0090","biotype":"protein_coding","ncbi_id":"23065","summary":"This gene encodes a single-pass type I transmembrane protein, which is a subunit of the endoplasmic reticulum membrane protein complex (EMC). Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2012]","start":19215664,"end":19251552,"strand":-1,"description":"ER membrane protein complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28957]"}, {"versioned_ensembl_gene_id":"ENSG00000230424.1","gene_symbol":"AL035413.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19210501,"end":19240704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223875.2","gene_symbol":"NBEAP3","gene_name":"neurobeachin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:40004]","synonyms":"BCL8C","biotype":"unprocessed_pseudogene","ncbi_id":"100418905","summary":null,"start":15852990,"end":15893942,"strand":1,"description":"neurobeachin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:40004]"}, {"versioned_ensembl_gene_id":"ENSG00000257950.3","gene_symbol":"P2RX5-TAX1BP3","gene_name":"P2RX5-TAX1BP3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49191]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533970","summary":"This locus represents naturally occurring read-through transcription between the neighboring P2RX5 (purinergic receptor P2X, ligand-gated ion channel, 5) and TAX1BP3 (Tax1 binding protein 3) genes on chromosome 17. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":3663063,"end":3696194,"strand":-1,"description":"P2RX5-TAX1BP3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49191]"}, {"versioned_ensembl_gene_id":"ENSG00000143322.19","gene_symbol":"ABL2","gene_name":"ABL proto-oncogene 2, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:77]","synonyms":"ARG,ABLL","biotype":"protein_coding","ncbi_id":"27","summary":"This gene encodes a member of the Abelson family of nonreceptor tyrosine protein kinases. The protein is highly similar to the c-abl oncogene 1 protein, including the tyrosine kinase, SH2 and SH3 domains, and it plays a role in cytoskeletal rearrangements through its C-terminal F-actin- and microtubule-binding sequences. This gene is expressed in both normal and tumor cells, and is involved in translocation with the ets variant 6 gene in leukemia. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Nov 2009]","start":179099327,"end":179229684,"strand":-1,"description":"ABL proto-oncogene 2, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:77]"}, {"versioned_ensembl_gene_id":"ENSG00000233264.2","gene_symbol":"AC006042.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7980312,"end":7982228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268922.1","gene_symbol":"AC012616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8778665,"end":8778861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226153.1","gene_symbol":"Z93242.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17705339,"end":17705691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278481.1","gene_symbol":"KIR2DL5B","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5B [Source:HGNC Symbol;Acc:HGNC:16346]","synonyms":"KIR2DL5.4,KIR2DL5.3,KIR2DL5.2,KIR2DL5","biotype":"protein_coding","ncbi_id":"553128","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54771247,"end":54780763,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5B [Source:HGNC Symbol;Acc:HGNC:16346]"}, {"versioned_ensembl_gene_id":"ENSG00000267259.1","gene_symbol":"AC061975.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28232590,"end":28235281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237575.4","gene_symbol":"PYY2","gene_name":"peptide YY 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9749]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"23615","summary":null,"start":28226563,"end":28228065,"strand":1,"description":"peptide YY 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9749]"}, {"versioned_ensembl_gene_id":"ENSG00000272660.1","gene_symbol":"AC090425.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179584271,"end":179584410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259239.1","gene_symbol":"AC021755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40133768,"end":40135214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182993.3","gene_symbol":"C12orf60","gene_name":"chromosome 12 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:28726]","synonyms":"MGC47869","biotype":"protein_coding","ncbi_id":"144608","summary":null,"start":14803572,"end":14906586,"strand":1,"description":"chromosome 12 open reading frame 60 [Source:HGNC Symbol;Acc:HGNC:28726]"}, {"versioned_ensembl_gene_id":"ENSG00000227365.1","gene_symbol":"AC008060.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155510283,"end":155518623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111339.10","gene_symbol":"ART4","gene_name":"ADP-ribosyltransferase 4 (Dombrock blood group) [Source:HGNC Symbol;Acc:HGNC:726]","synonyms":"DOK1,DO,CD297","biotype":"protein_coding","ncbi_id":"420","summary":"This gene encodes a protein that contains a mono-ADP-ribosylation (ART) motif. It is a member of the ADP-ribosyltransferase gene family but enzymatic activity has not been demonstrated experimentally. Antigens of the Dombrock blood group system are located on the gene product, which is glycosylphosphatidylinosotol-anchored to the erythrocyte membrane. Allelic variants, some of which lead to adverse transfusion reactions, are known. [provided by RefSeq, Jul 2008]","start":14825569,"end":14843495,"strand":-1,"description":"ADP-ribosyltransferase 4 (Dombrock blood group) [Source:HGNC Symbol;Acc:HGNC:726]"}, {"versioned_ensembl_gene_id":"ENSG00000179256.2","gene_symbol":"SMCO3","gene_name":"single-pass membrane protein with coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:34401]","synonyms":"C12orf69,LOC440087","biotype":"protein_coding","ncbi_id":"440087","summary":null,"start":14804650,"end":14814182,"strand":-1,"description":"single-pass membrane protein with coiled-coil domains 3 [Source:HGNC Symbol;Acc:HGNC:34401]"}, {"versioned_ensembl_gene_id":"ENSG00000278605.4","gene_symbol":"TSEN34","gene_name":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]","synonyms":"LENG5,SEN34,SEN34,SEN34L,SEN34L,LENG5","biotype":"protein_coding","ncbi_id":"79042","summary":"This gene encodes a catalytic subunit of the tRNA splicing endonuclease, which catalyzes the removal of introns from precursor tRNAs. The endonuclease complex is also associated with a pre-mRNA 3-prime end processing factor. A mutation in this gene results in the neurological disorder pontocerebellar hypoplasia type 2. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Oct 2009]","start":54190536,"end":54194332,"strand":1,"description":"tRNA splicing endonuclease subunit 34 [Source:HGNC Symbol;Acc:HGNC:15506]"}, {"versioned_ensembl_gene_id":"ENSG00000103415.11","gene_symbol":"HMOX2","gene_name":"heme oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:5014]","synonyms":"HO-2","biotype":"protein_coding","ncbi_id":"3163","summary":"Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. Several alternatively spliced transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":4474690,"end":4510347,"strand":1,"description":"heme oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:5014]"}, {"versioned_ensembl_gene_id":"ENSG00000227012.2","gene_symbol":"LINC02527","gene_name":"long intergenic non-protein coding RNA 2527 [Source:HGNC Symbol;Acc:HGNC:53553]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377946","summary":null,"start":111900489,"end":111901851,"strand":-1,"description":"long intergenic non-protein coding RNA 2527 [Source:HGNC Symbol;Acc:HGNC:53553]"}, {"versioned_ensembl_gene_id":"ENSG00000157087.17","gene_symbol":"ATP2B2","gene_name":"ATPase plasma membrane Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:815]","synonyms":"PMCA2","biotype":"protein_coding","ncbi_id":"491","summary":"The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 2. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":10324023,"end":10708031,"strand":-1,"description":"ATPase plasma membrane Ca2+ transporting 2 [Source:HGNC Symbol;Acc:HGNC:815]"}, {"versioned_ensembl_gene_id":"ENSG00000240651.1","gene_symbol":"SEPT7P4","gene_name":"septin 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38039]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418715","summary":null,"start":63241590,"end":63248321,"strand":-1,"description":"septin 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38039]"}, {"versioned_ensembl_gene_id":"ENSG00000243961.2","gene_symbol":"AL109754.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9986088,"end":10007116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228075.4","gene_symbol":"BOD1L2","gene_name":"biorientation of chromosomes in cell division 1 like 2 [Source:HGNC Symbol;Acc:HGNC:28505]","synonyms":"MGC33608,FAM44C,BOD1P","biotype":"protein_coding","ncbi_id":"284257","summary":null,"start":57147062,"end":57150300,"strand":1,"description":"biorientation of chromosomes in cell division 1 like 2 [Source:HGNC Symbol;Acc:HGNC:28505]"}, {"versioned_ensembl_gene_id":"ENSG00000118245.2","gene_symbol":"TNP1","gene_name":"transition protein 1 [Source:HGNC Symbol;Acc:HGNC:11951]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7141","summary":"Transition protein-1 is a spermatid-specific product of the haploid genome which replaces histone and is itself replaced in the mature sperm by the protamines (see PRM1, MIM 182880; PRM2, MIM 182890) (Luerssen et al., 1990 [PubMed 2249851]).[supplied by OMIM, Mar 2008]","start":216859458,"end":216860064,"strand":-1,"description":"transition protein 1 [Source:HGNC Symbol;Acc:HGNC:11951]"}, {"versioned_ensembl_gene_id":"ENSG00000267789.1","gene_symbol":"AC100775.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57136322,"end":57146998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231597.1","gene_symbol":"AC007557.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216854389,"end":216855132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253127.1","gene_symbol":"IGKV2D-36","gene_name":"immunoglobulin kappa variable 2D-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5802]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28880","summary":null,"start":89887022,"end":89887247,"strand":1,"description":"immunoglobulin kappa variable 2D-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5802]"}, {"versioned_ensembl_gene_id":"ENSG00000256400.1","gene_symbol":"AC018630.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11097179,"end":11097274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237479.1","gene_symbol":"AC007557.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216866332,"end":216867813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110841.13","gene_symbol":"PPFIBP1","gene_name":"PPFIA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9249]","synonyms":"SGT2,L2,hSgt2p,hSGT2","biotype":"protein_coding","ncbi_id":"8496","summary":"The protein encoded by this gene is a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. Liprins interact with members of LAR family of transmembrane protein tyrosine phosphatases, which are known to be important for axon guidance and mammary gland development. It has been proposed that liprins are multivalent proteins that form complex structures and act as scaffolds for the recruitment and anchoring of LAR family of tyrosine phosphatases. This protein was found to interact with S100A4, a calcium-binding protein related to tumor invasiveness and metastasis. In vitro experiment demonstrated that the interaction inhibited the phosphorylation of this protein by protein kinase C and protein kinase CK2. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":27523431,"end":27695564,"strand":1,"description":"PPFIA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9249]"}, {"versioned_ensembl_gene_id":"ENSG00000240031.1","gene_symbol":"OR9A3P","gene_name":"olfactory receptor family 9 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15094]","synonyms":"OR9A6P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"392106","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":141862860,"end":141863737,"strand":1,"description":"olfactory receptor family 9 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15094]"}, {"versioned_ensembl_gene_id":"ENSG00000165092.12","gene_symbol":"ALDH1A1","gene_name":"aldehyde dehydrogenase 1 family member A1 [Source:HGNC Symbol;Acc:HGNC:402]","synonyms":"RALDH1,PUMB1,ALDH1","biotype":"protein_coding","ncbi_id":"216","summary":"The protein encoded by this gene belongs to the aldehyde dehydrogenase family. Aldehyde dehydrogenase is the next enzyme after alcohol dehydrogenase in the major pathway of alcohol metabolism. There are two major aldehyde dehydrogenase isozymes in the liver, cytosolic and mitochondrial, which are encoded by distinct genes, and can be distinguished by their electrophoretic mobility, kinetic properties, and subcellular localization. This gene encodes the cytosolic isozyme. Studies in mice show that through its role in retinol metabolism, this gene may also be involved in the regulation of the metabolic responses to high-fat diet. [provided by RefSeq, Mar 2011]","start":72900662,"end":73080442,"strand":-1,"description":"aldehyde dehydrogenase 1 family member A1 [Source:HGNC Symbol;Acc:HGNC:402]"}, {"versioned_ensembl_gene_id":"ENSG00000231887.6","gene_symbol":"PRH1","gene_name":"proline rich protein HaeIII subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9366]","synonyms":"Pa","biotype":"protein_coding","ncbi_id":"5554","summary":"This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. Multiple distinct alleles of this locus including the parotid isoelectric-focusing variant slow (PIF-s), the parotid acidic protein (Pa), and the double band slow (Db-s) isoforms have been characterized. The reference genome encodes the Db-s allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Co-transcription of this gene with adjacent genes has been observed. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]","start":10824960,"end":11171544,"strand":-1,"description":"proline rich protein HaeIII subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9366]"}, {"versioned_ensembl_gene_id":"ENSG00000277015.4","gene_symbol":"SALL3","gene_name":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]","synonyms":"ZNF796","biotype":"protein_coding","ncbi_id":"27164","summary":"This gene encodes a sal-like C2H2-type zinc-finger protein, and belongs to a family of evolutionarily conserved genes found in species as diverse as Drosophila, C. elegans, and vertebrates. Mutations in some of these genes are associated with congenital disorders in human, suggesting their importance in embryonic development. This protein binds to DNA methyltransferase 3 alpha (DNMT3A), and reduces DNMT3A-mediated CpG island methylation. It is suggested that silencing of this gene, resulting in acceleration of DNA methylation, may have a role in oncogenesis. [provided by RefSeq, Oct 2011]","start":78980275,"end":79002677,"strand":1,"description":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]"}, {"versioned_ensembl_gene_id":"ENSG00000240774.1","gene_symbol":"AC126182.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120484171,"end":120484527,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236934.1","gene_symbol":"AL844213.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30505760,"end":30508714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277901.1","gene_symbol":"AL390037.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23320958,"end":23325352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237236.1","gene_symbol":"AC023141.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57822201,"end":57822942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269934.1","gene_symbol":"AL353593.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228274584,"end":228276066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169218.13","gene_symbol":"RSPO1","gene_name":"R-spondin 1 [Source:HGNC Symbol;Acc:HGNC:21679]","synonyms":"RSPONDIN,FLJ40906","biotype":"protein_coding","ncbi_id":"284654","summary":"This gene encodes a secreted activator protein with two cysteine-rich, furin-like domains and one thrombospondin type 1 domain. The encoded protein is a ligand for leucine-rich repeat-containing G-protein coupled receptors (LGR proteins) and positively regulates the Wnt signaling pathway. In mice, the protein induces the rapid onset of crypt cell proliferation and increases intestinal epithelial healing, providing a protective effect against chemotherapy-induced adverse effects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":37611350,"end":37634923,"strand":-1,"description":"R-spondin 1 [Source:HGNC Symbol;Acc:HGNC:21679]"}, {"versioned_ensembl_gene_id":"ENSG00000251546.1","gene_symbol":"IGKV1D-39","gene_name":"immunoglobulin kappa variable 1D-39 [Source:HGNC Symbol;Acc:HGNC:5756]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28893","summary":null,"start":89862482,"end":89862981,"strand":1,"description":"immunoglobulin kappa variable 1D-39 [Source:HGNC Symbol;Acc:HGNC:5756]"}, {"versioned_ensembl_gene_id":"ENSG00000255457.1","gene_symbol":"AC022880.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13695574,"end":13705506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233263.1","gene_symbol":"AC009518.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131892616,"end":131893615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251563.1","gene_symbol":"IARS2P1","gene_name":"isoleucyl-tRNA synthetase 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642461","summary":null,"start":87598462,"end":87601634,"strand":-1,"description":"isoleucyl-tRNA synthetase 2, mitochondrial pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50474]"}, {"versioned_ensembl_gene_id":"ENSG00000282127.1","gene_symbol":"IGHVII-22-1","gene_name":"immunoglobulin heavy variable (II)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5673]","synonyms":"IGHV(II)-22-1","biotype":"IG_V_pseudogene","ncbi_id":"28374","summary":null,"start":106264133,"end":106264397,"strand":-1,"description":"immunoglobulin heavy variable (II)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5673]"}, {"versioned_ensembl_gene_id":"ENSG00000232024.2","gene_symbol":"LSM12P1","gene_name":"LSM12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32453]","synonyms":"LSM12P","biotype":"processed_pseudogene","ncbi_id":"653122","summary":null,"start":35525176,"end":35525763,"strand":-1,"description":"LSM12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32453]"}, {"versioned_ensembl_gene_id":"ENSG00000232758.1","gene_symbol":"HCG27","gene_name":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]","synonyms":"bPG299F13.9,FLJ40123,bCX101P6.9,bQB115I13.2","biotype":"processed_transcript","ncbi_id":"253018","summary":null,"start":31190323,"end":31196527,"strand":1,"description":"HLA complex group 27 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:27366]"}, {"versioned_ensembl_gene_id":"ENSG00000228583.1","gene_symbol":"AL662833.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31192728,"end":31194480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274571.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"CLR19.4,NALP7,PAN7,PYPAF3,NALP7,NOD12,PYPAF3,CLR19.4,NOD12,PAN7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54931624,"end":54974427,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000162437.14","gene_symbol":"RAVER2","gene_name":"ribonucleoprotein, PTB binding 2 [Source:HGNC Symbol;Acc:HGNC:25577]","synonyms":"KIAA1579,FLJ10770","biotype":"protein_coding","ncbi_id":"55225","summary":null,"start":64745095,"end":64833232,"strand":1,"description":"ribonucleoprotein, PTB binding 2 [Source:HGNC Symbol;Acc:HGNC:25577]"}, {"versioned_ensembl_gene_id":"ENSG00000253547.2","gene_symbol":"AP001858.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63046785,"end":63048126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270456.1","gene_symbol":"AL670379.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120981529,"end":120981779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242362.2","gene_symbol":"CT47A2","gene_name":"cancer/testis antigen family 47, member A2 [Source:HGNC Symbol;Acc:HGNC:33283]","synonyms":"CT47.2","biotype":"protein_coding","ncbi_id":"728090","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120977606,"end":120980928,"strand":-1,"description":"cancer/testis antigen family 47, member A2 [Source:HGNC Symbol;Acc:HGNC:33283]"}, {"versioned_ensembl_gene_id":"ENSG00000284670.1","gene_symbol":"AC092128.1","gene_name":null,"synonyms":null,"biotype":"translated_processed_pseudogene","ncbi_id":null,"summary":null,"start":73940639,"end":73941781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282417.1","gene_symbol":"HERC2P9","gene_name":"hect domain and RLD 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30495]","synonyms":"FLJ59185","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440248","summary":null,"start":28731693,"end":28826770,"strand":1,"description":"hect domain and RLD 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30495]"}, {"versioned_ensembl_gene_id":"ENSG00000253320.5","gene_symbol":"AZIN1-AS1","gene_name":"AZIN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51558]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506753","summary":null,"start":102864300,"end":102977876,"strand":1,"description":"AZIN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51558]"}, {"versioned_ensembl_gene_id":"ENSG00000237262.1","gene_symbol":"AC068492.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136077892,"end":136078513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258724.1","gene_symbol":"AC105001.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10725399,"end":10839847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258725.1","gene_symbol":"PRC1-AS1","gene_name":"PRC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48587]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507118","summary":null,"start":90966345,"end":90988624,"strand":1,"description":"PRC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48587]"}, {"versioned_ensembl_gene_id":"ENSG00000237381.2","gene_symbol":"AL023280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93388075,"end":93389497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258779.7","gene_symbol":"LINC01568","gene_name":"long intergenic non-protein coding RNA 1568 [Source:HGNC Symbol;Acc:HGNC:51371]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506172","summary":null,"start":73386805,"end":73504954,"strand":1,"description":"long intergenic non-protein coding RNA 1568 [Source:HGNC Symbol;Acc:HGNC:51371]"}, {"versioned_ensembl_gene_id":"ENSG00000254206.5","gene_symbol":"NPIPB11","gene_name":"nuclear pore complex interacting protein family member B11 [Source:HGNC Symbol;Acc:HGNC:37453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728888","summary":null,"start":29381354,"end":29404029,"strand":-1,"description":"nuclear pore complex interacting protein family member B11 [Source:HGNC Symbol;Acc:HGNC:37453]"}, {"versioned_ensembl_gene_id":"ENSG00000106511.5","gene_symbol":"MEOX2","gene_name":"mesenchyme homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7014]","synonyms":"MOX2,GAX","biotype":"protein_coding","ncbi_id":"4223","summary":"This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [provided by RefSeq, Jul 2008]","start":15611212,"end":15686812,"strand":-1,"description":"mesenchyme homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7014]"}, {"versioned_ensembl_gene_id":"ENSG00000273756.4","gene_symbol":"AC100756.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23326256,"end":23334127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158882.14","gene_symbol":"TOMM40L","gene_name":"translocase of outer mitochondrial membrane 40 like [Source:HGNC Symbol;Acc:HGNC:25756]","synonyms":"TOMM40B,FLJ12770","biotype":"protein_coding","ncbi_id":"84134","summary":null,"start":161225939,"end":161230744,"strand":1,"description":"translocase of outer mitochondrial membrane 40 like [Source:HGNC Symbol;Acc:HGNC:25756]"}, {"versioned_ensembl_gene_id":"ENSG00000283023.1","gene_symbol":"AC116618.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12602466,"end":12626642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230276.2","gene_symbol":"AL162388.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29254075,"end":29254426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224354.2","gene_symbol":"MTND2P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42106]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873176","summary":null,"start":141802482,"end":141803487,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42106]"}, {"versioned_ensembl_gene_id":"ENSG00000278541.1","gene_symbol":"AC116165.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23193491,"end":23193696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220685.3","gene_symbol":"AL139094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5065795,"end":5066982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229060.4","gene_symbol":"AL451124.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28148211,"end":28149236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273962.1","gene_symbol":"IGKV2-40","gene_name":"immunoglobulin kappa variable 2-40 [Source:HGNC Symbol;Acc:HGNC:5789]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28916","summary":null,"start":89330110,"end":89330429,"strand":-1,"description":"immunoglobulin kappa variable 2-40 [Source:HGNC Symbol;Acc:HGNC:5789]"}, {"versioned_ensembl_gene_id":"ENSG00000223836.1","gene_symbol":"AC023141.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57820032,"end":57820410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223864.1","gene_symbol":"NPM1P19","gene_name":"nucleophosmin 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:7921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10828","summary":null,"start":38977711,"end":38978422,"strand":-1,"description":"nucleophosmin 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:7921]"}, {"versioned_ensembl_gene_id":"ENSG00000077420.15","gene_symbol":"APBB1IP","gene_name":"amyloid beta precursor protein binding family B member 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:17379]","synonyms":"RIAM,INAG1","biotype":"protein_coding","ncbi_id":"54518","summary":null,"start":26438203,"end":26567803,"strand":1,"description":"amyloid beta precursor protein binding family B member 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:17379]"}, {"versioned_ensembl_gene_id":"ENSG00000182518.13","gene_symbol":"FAM104B","gene_name":"family with sequence similarity 104 member B [Source:HGNC Symbol;Acc:HGNC:25085]","synonyms":"FLJ20434,CXorf44","biotype":"protein_coding","ncbi_id":"90736","summary":null,"start":55143102,"end":55161310,"strand":-1,"description":"family with sequence similarity 104 member B [Source:HGNC Symbol;Acc:HGNC:25085]"}, {"versioned_ensembl_gene_id":"ENSG00000226845.1","gene_symbol":"EEF1GP3","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44558]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651628","summary":null,"start":40596207,"end":40597494,"strand":-1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44558]"}, {"versioned_ensembl_gene_id":"ENSG00000251131.1","gene_symbol":"AC025171.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43018429,"end":43024247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224089.3","gene_symbol":"CT47A10","gene_name":"cancer/testis antigen family 47, member A10 [Source:HGNC Symbol;Acc:HGNC:33291]","synonyms":"CT47.10","biotype":"protein_coding","ncbi_id":"728036","summary":null,"start":120938701,"end":120942023,"strand":-1,"description":"cancer/testis antigen family 47, member A10 [Source:HGNC Symbol;Acc:HGNC:33291]"}, {"versioned_ensembl_gene_id":"ENSG00000235540.6","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAP1-AS1,XXbac-BPG246D15.8,TAPSAR1","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32766404,"end":32768813,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000266771.1","gene_symbol":"AC015688.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27675894,"end":27675997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237034.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30404207,"end":30408812,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000249417.1","gene_symbol":"AC117383.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141267353,"end":141367137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282673.1","gene_symbol":"PRB1","gene_name":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]","synonyms":"PRB1M,PRB1L,PMS,PMF,PM","biotype":"protein_coding","ncbi_id":"5542","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Medium\" allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015]","start":11348080,"end":11351848,"strand":-1,"description":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]"}, {"versioned_ensembl_gene_id":"ENSG00000214773.1","gene_symbol":"AC112512.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47601715,"end":47604677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283047.1","gene_symbol":"CU459211.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10939388,"end":10961338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230109.1","gene_symbol":"AL158209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21340233,"end":21372950,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250572.1","gene_symbol":"AC108516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87261931,"end":87266822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228860.1","gene_symbol":"AL731547.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21217891,"end":21218279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116191.17","gene_symbol":"RALGPS2","gene_name":"Ral GEF with PH domain and SH3 binding motif 2 [Source:HGNC Symbol;Acc:HGNC:30279]","synonyms":"KIAA0351,FLJ25604,FLJ10244","biotype":"protein_coding","ncbi_id":"55103","summary":null,"start":178725147,"end":178921841,"strand":1,"description":"Ral GEF with PH domain and SH3 binding motif 2 [Source:HGNC Symbol;Acc:HGNC:30279]"}, {"versioned_ensembl_gene_id":"ENSG00000158966.13","gene_symbol":"CACHD1","gene_name":"cache domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29314]","synonyms":"VWCD1,KIAA1573","biotype":"protein_coding","ncbi_id":"57685","summary":null,"start":64470792,"end":64693058,"strand":1,"description":"cache domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29314]"}, {"versioned_ensembl_gene_id":"ENSG00000204221.11","gene_symbol":"WDR46","gene_name":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]","synonyms":"BING4,UTP7,C6orf11","biotype":"protein_coding","ncbi_id":"9277","summary":null,"start":33200708,"end":33211131,"strand":-1,"description":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]"}, {"versioned_ensembl_gene_id":"ENSG00000175463.11","gene_symbol":"TBC1D10C","gene_name":"TBC1 domain family member 10C [Source:HGNC Symbol;Acc:HGNC:24702]","synonyms":"FLJ00332,EPI64C,Carabin","biotype":"protein_coding","ncbi_id":"374403","summary":"The protein encoded by this gene has an N-terminal Rab-GTPase domain and a binding site at the C-terminus for calcineurin, and is an inhibitor of both the Ras signaling pathway and calcineurin, a phosphatase regulated by calcium and calmodulin. Genes encoding similar proteins are located on chromosomes 16 and 22. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013]","start":67403915,"end":67410089,"strand":1,"description":"TBC1 domain family member 10C [Source:HGNC Symbol;Acc:HGNC:24702]"}, {"versioned_ensembl_gene_id":"ENSG00000231514.1","gene_symbol":"FAM58CP","gene_name":"family with sequence similarity 58 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38436]","synonyms":"FAM58Y,FAM58AP1","biotype":"processed_pseudogene","ncbi_id":"100421487","summary":null,"start":26626520,"end":26627159,"strand":-1,"description":"family with sequence similarity 58 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:38436]"}, {"versioned_ensembl_gene_id":"ENSG00000180096.11","gene_symbol":"SEPT1","gene_name":"septin 1 [Source:HGNC Symbol;Acc:HGNC:2879]","synonyms":"PNUTL3,DIFF6","biotype":"protein_coding","ncbi_id":"1731","summary":"This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]","start":30378133,"end":30395991,"strand":-1,"description":"septin 1 [Source:HGNC Symbol;Acc:HGNC:2879]"}, {"versioned_ensembl_gene_id":"ENSG00000115539.13","gene_symbol":"PDCL3","gene_name":"phosducin like 3 [Source:HGNC Symbol;Acc:HGNC:28860]","synonyms":"VIAF1","biotype":"protein_coding","ncbi_id":"79031","summary":"This gene encodes a member of the phosducin-like protein family and is a putative modulator of heterotrimeric G proteins. The protein shares extensive amino acid sequence homology with phosducin. Members of the phosducin-like protein family have been shown to bind to the beta-gamma subunits of G proteins. [provided by RefSeq, Jul 2008]","start":100562690,"end":100576735,"strand":1,"description":"phosducin like 3 [Source:HGNC Symbol;Acc:HGNC:28860]"}, {"versioned_ensembl_gene_id":"ENSG00000253258.1","gene_symbol":"AC068228.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123181638,"end":123182788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235695.1","gene_symbol":"AC130472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47663626,"end":47663934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164167.10","gene_symbol":"LSM6","gene_name":"LSM6 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17017]","synonyms":"YDR378C","biotype":"protein_coding","ncbi_id":"11157","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]","start":146175685,"end":146200000,"strand":1,"description":"LSM6 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17017]"}, {"versioned_ensembl_gene_id":"ENSG00000267165.1","gene_symbol":"CHMP1B-AS1","gene_name":"CHMP1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52778]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"109729129","summary":null,"start":11851414,"end":11852751,"strand":-1,"description":"CHMP1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52778]"}, {"versioned_ensembl_gene_id":"ENSG00000054219.10","gene_symbol":"LY75","gene_name":"lymphocyte antigen 75 [Source:HGNC Symbol;Acc:HGNC:6729]","synonyms":"DEC-205,CLEC13B,CD205","biotype":"protein_coding","ncbi_id":"4065","summary":null,"start":159803355,"end":159904749,"strand":-1,"description":"lymphocyte antigen 75 [Source:HGNC Symbol;Acc:HGNC:6729]"}, {"versioned_ensembl_gene_id":"ENSG00000277090.2","gene_symbol":"GOLGA8G","gene_name":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]","synonyms":"DKFZp434K052","biotype":"protein_coding","ncbi_id":"283768","summary":null,"start":28661119,"end":28674479,"strand":-1,"description":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]"}, {"versioned_ensembl_gene_id":"ENSG00000182831.11","gene_symbol":"C16orf72","gene_name":"chromosome 16 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:30103]","synonyms":"PRO0149,FLJ41272","biotype":"protein_coding","ncbi_id":"29035","summary":null,"start":9091648,"end":9121640,"strand":1,"description":"chromosome 16 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:30103]"}, {"versioned_ensembl_gene_id":"ENSG00000263244.2","gene_symbol":"AC087190.4","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":9104848,"end":9113181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224713.4","gene_symbol":"AC025165.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57612118,"end":57619638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260349.1","gene_symbol":"AC087190.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9105834,"end":9107174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248809.5","gene_symbol":"LINC01095","gene_name":"long intergenic non-protein coding RNA 1095 [Source:HGNC Symbol;Acc:HGNC:49220]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505545","summary":null,"start":146109455,"end":146121913,"strand":-1,"description":"long intergenic non-protein coding RNA 1095 [Source:HGNC Symbol;Acc:HGNC:49220]"}, {"versioned_ensembl_gene_id":"ENSG00000275621.3","gene_symbol":"AC139677.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46805899,"end":46851260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230531.1","gene_symbol":"MTND5P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873197","summary":null,"start":57194257,"end":57196054,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42269]"}, {"versioned_ensembl_gene_id":"ENSG00000283626.1","gene_symbol":"AC099654.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57190461,"end":57191138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226560.10","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31974264,"end":32022117,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000100138.13","gene_symbol":"SNU13","gene_name":"small nuclear ribonucleoprotein 13 [Source:HGNC Symbol;Acc:HGNC:7819]","synonyms":"FA-1,15.5K,SSFA1,SPAG12,SNRNP15-5,NHP2L1","biotype":"protein_coding","ncbi_id":"4809","summary":"Originally named because of its sequence similarity to the Saccharomyces cerevisiae NHP2 (non-histone protein 2), this protein appears to be a highly conserved nuclear protein that is a component of the [U4/U6.U5] tri-snRNP. It binds to the 5' stem-loop of U4 snRNA. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":41673930,"end":41690504,"strand":-1,"description":"small nuclear ribonucleoprotein 13 [Source:HGNC Symbol;Acc:HGNC:7819]"}, {"versioned_ensembl_gene_id":"ENSG00000273580.1","gene_symbol":"AC087072.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35933888,"end":35934569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260612.1","gene_symbol":"AC009097.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71726975,"end":71727992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282023.1","gene_symbol":"AC243913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28636485,"end":28636692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204188.7","gene_symbol":"GGNBP1","gene_name":"gametogenetin binding protein 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19427]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"449520","summary":"This gene is the ortholog of the mouse gametogenetin-binding protein 1 gene. In human, the open reading frame is disrupted by a nonsense mutation after 8-aa; consequently, this gene is currently considered to be a unitary pseudogene in human even though it is functional in other mammals. [provided by RefSeq, Aug 2009]","start":33540046,"end":33589026,"strand":1,"description":"gametogenetin binding protein 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19427]"}, {"versioned_ensembl_gene_id":"ENSG00000262113.1","gene_symbol":"AC010614.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34303449,"end":34303913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242159.1","gene_symbol":"ABCF2P1","gene_name":"ATP binding cassette subfamily F member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48841]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344653","summary":null,"start":88317156,"end":88319022,"strand":1,"description":"ATP binding cassette subfamily F member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48841]"}, {"versioned_ensembl_gene_id":"ENSG00000253595.5","gene_symbol":"LINC01300","gene_name":"long intergenic non-protein coding RNA 1300 [Source:HGNC Symbol;Acc:HGNC:50460]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"731779","summary":null,"start":141340549,"end":141344621,"strand":1,"description":"long intergenic non-protein coding RNA 1300 [Source:HGNC Symbol;Acc:HGNC:50460]"}, {"versioned_ensembl_gene_id":"ENSG00000197245.5","gene_symbol":"FAM110D","gene_name":"family with sequence similarity 110 member D [Source:HGNC Symbol;Acc:HGNC:25860]","synonyms":"GRRP1,FLJ14050","biotype":"protein_coding","ncbi_id":"79927","summary":null,"start":26159020,"end":26163962,"strand":1,"description":"family with sequence similarity 110 member D [Source:HGNC Symbol;Acc:HGNC:25860]"}, {"versioned_ensembl_gene_id":"ENSG00000257741.5","gene_symbol":"LINC01490","gene_name":"long intergenic non-protein coding RNA 1490 [Source:HGNC Symbol;Acc:HGNC:51146]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928420","summary":null,"start":80763154,"end":80770717,"strand":1,"description":"long intergenic non-protein coding RNA 1490 [Source:HGNC Symbol;Acc:HGNC:51146]"}, {"versioned_ensembl_gene_id":"ENSG00000189223.14","gene_symbol":"PAX8-AS1","gene_name":"PAX8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49271]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"654433","summary":null,"start":113211522,"end":113276581,"strand":1,"description":"PAX8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49271]"}, {"versioned_ensembl_gene_id":"ENSG00000224379.6","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31151089,"end":31156758,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000281536.1","gene_symbol":"AC009286.3","gene_name":"Immunoglobulin lambda variable 5-39 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JS06]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":22402588,"end":22403079,"strand":1,"description":"Immunoglobulin lambda variable 5-39 [Source:UniProtKB/Swiss-Prot;Acc:A0A0G2JS06]"}, {"versioned_ensembl_gene_id":"ENSG00000170500.12","gene_symbol":"LONRF2","gene_name":"LON peptidase N-terminal domain and ring finger 2 [Source:HGNC Symbol;Acc:HGNC:24788]","synonyms":"FLJ45273,RNF192","biotype":"protein_coding","ncbi_id":"164832","summary":null,"start":100273291,"end":100322733,"strand":-1,"description":"LON peptidase N-terminal domain and ring finger 2 [Source:HGNC Symbol;Acc:HGNC:24788]"}, {"versioned_ensembl_gene_id":"ENSG00000253257.1","gene_symbol":"MTND4P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42234]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873195","summary":null,"start":13353401,"end":13353530,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42234]"}, {"versioned_ensembl_gene_id":"ENSG00000164379.6","gene_symbol":"FOXQ1","gene_name":"forkhead box Q1 [Source:HGNC Symbol;Acc:HGNC:20951]","synonyms":"HFH1","biotype":"protein_coding","ncbi_id":"94234","summary":"FOXQ1 is a member of the FOX gene family, which is characterized by a conserved 110-amino acid DNA-binding motif called the forkhead or winged helix domain. FOX genes are involved in embryonic development, cell cycle regulation, tissue-specific gene expression, cell signaling, and tumorigenesis (Bieller et al., 2001 [PubMed 11747606]).[supplied by OMIM, May 2009]","start":1312440,"end":1314748,"strand":1,"description":"forkhead box Q1 [Source:HGNC Symbol;Acc:HGNC:20951]"}, {"versioned_ensembl_gene_id":"ENSG00000228845.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32629554,"end":32630385,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000233965.1","gene_symbol":"CT009531.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31595070,"end":31595649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227019.2","gene_symbol":"OR7E101P","gene_name":"olfactory receptor family 7 subfamily E member 101 pseudogene [Source:HGNC Symbol;Acc:HGNC:15342]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81138","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":46460609,"end":46461121,"strand":1,"description":"olfactory receptor family 7 subfamily E member 101 pseudogene [Source:HGNC Symbol;Acc:HGNC:15342]"}, {"versioned_ensembl_gene_id":"ENSG00000205726.14","gene_symbol":"ITSN1","gene_name":"intersectin 1 [Source:HGNC Symbol;Acc:HGNC:6183]","synonyms":"SH3P17,SH3D1A,MGC134949,MGC134948,ITSN","biotype":"protein_coding","ncbi_id":"6453","summary":"The protein encoded by this gene is a cytoplasmic membrane-associated protein that indirectly coordinates endocytic membrane traffic with the actin assembly machinery. In addition, the encoded protein may regulate the formation of clathrin-coated vesicles and could be involved in synaptic vesicle recycling. This protein has been shown to interact with dynamin, CDC42, SNAP23, SNAP25, SPIN90, EPS15, EPN1, EPN2, and STN2. Multiple transcript variants encoding different isoforms have been found for this gene, but the full-length nature of only two of them have been characterized so far. [provided by RefSeq, Jul 2008]","start":33642400,"end":33899861,"strand":1,"description":"intersectin 1 [Source:HGNC Symbol;Acc:HGNC:6183]"}, {"versioned_ensembl_gene_id":"ENSG00000235277.1","gene_symbol":"AF127577.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14918534,"end":14947096,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091164.12","gene_symbol":"TXNL1","gene_name":"thioredoxin like 1 [Source:HGNC Symbol;Acc:HGNC:12436]","synonyms":"TXNL,Txl,TRP32","biotype":"protein_coding","ncbi_id":"9352","summary":null,"start":56597208,"end":56651600,"strand":-1,"description":"thioredoxin like 1 [Source:HGNC Symbol;Acc:HGNC:12436]"}, {"versioned_ensembl_gene_id":"ENSG00000231201.1","gene_symbol":"AF127577.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14971470,"end":14992854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234583.1","gene_symbol":"TSPY19P","gene_name":"testis specific protein, Y-linked 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:37998]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132504","summary":null,"start":6303957,"end":6305074,"strand":-1,"description":"testis specific protein, Y-linked 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:37998]"}, {"versioned_ensembl_gene_id":"ENSG00000275352.1","gene_symbol":"AC006335.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6273579,"end":6274065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156026.14","gene_symbol":"MCU","gene_name":"mitochondrial calcium uniporter [Source:HGNC Symbol;Acc:HGNC:23526]","synonyms":"FLJ46135,CCDC109A,C10orf42","biotype":"protein_coding","ncbi_id":"90550","summary":"This gene encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":72692131,"end":72887694,"strand":1,"description":"mitochondrial calcium uniporter [Source:HGNC Symbol;Acc:HGNC:23526]"}, {"versioned_ensembl_gene_id":"ENSG00000262332.1","gene_symbol":"AC136624.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16223027,"end":16224261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272627.1","gene_symbol":"AC016542.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":72766560,"end":72767052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131943.17","gene_symbol":"C19orf12","gene_name":"chromosome 19 open reading frame 12 [Source:HGNC Symbol;Acc:HGNC:25443]","synonyms":"SPG43,NBIA4,MPAN,MGC10922,DKFZP762D096","biotype":"protein_coding","ncbi_id":"83636","summary":"This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":29698886,"end":29715789,"strand":-1,"description":"chromosome 19 open reading frame 12 [Source:HGNC Symbol;Acc:HGNC:25443]"}, {"versioned_ensembl_gene_id":"ENSG00000142149.8","gene_symbol":"HUNK","gene_name":"hormonally up-regulated Neu-associated kinase [Source:HGNC Symbol;Acc:HGNC:13326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"30811","summary":null,"start":31873315,"end":32044633,"strand":1,"description":"hormonally up-regulated Neu-associated kinase [Source:HGNC Symbol;Acc:HGNC:13326]"}, {"versioned_ensembl_gene_id":"ENSG00000230616.4","gene_symbol":"PPIAP9","gene_name":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]","synonyms":"PPIP9,Em:AC006046.3","biotype":"processed_pseudogene","ncbi_id":"5491","summary":null,"start":31586437,"end":31587248,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:9272]"}, {"versioned_ensembl_gene_id":"ENSG00000166289.5","gene_symbol":"PLEKHF1","gene_name":"pleckstrin homology and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20764]","synonyms":"ZFYVE15,PHAFIN1,MGC4090,APPD","biotype":"protein_coding","ncbi_id":"79156","summary":null,"start":29665056,"end":29675457,"strand":1,"description":"pleckstrin homology and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20764]"}, {"versioned_ensembl_gene_id":"ENSG00000283991.1","gene_symbol":"AC017000.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4130181,"end":4134837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234925.2","gene_symbol":"ATP5HP4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49626]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246723","summary":null,"start":68642519,"end":68642993,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49626]"}, {"versioned_ensembl_gene_id":"ENSG00000234040.3","gene_symbol":"RPL10P12","gene_name":"ribosomal protein L10 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645422","summary":null,"start":68626870,"end":68627187,"strand":-1,"description":"ribosomal protein L10 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52345]"}, {"versioned_ensembl_gene_id":"ENSG00000198865.9","gene_symbol":"CCDC152","gene_name":"coiled-coil domain containing 152 [Source:HGNC Symbol;Acc:HGNC:34438]","synonyms":"LOC100129792","biotype":"protein_coding","ncbi_id":"100129792","summary":null,"start":42756801,"end":42802360,"strand":1,"description":"coiled-coil domain containing 152 [Source:HGNC Symbol;Acc:HGNC:34438]"}, {"versioned_ensembl_gene_id":"ENSG00000119125.16","gene_symbol":"GDA","gene_name":"guanine deaminase [Source:HGNC Symbol;Acc:HGNC:4212]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9615","summary":"This gene encodes an enzyme responsible for the hydrolytic deamination of guanine. Studies in rat ortholog suggest this gene plays a role in microtubule assembly. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":72114595,"end":72257193,"strand":1,"description":"guanine deaminase [Source:HGNC Symbol;Acc:HGNC:4212]"}, {"versioned_ensembl_gene_id":"ENSG00000138119.16","gene_symbol":"MYOF","gene_name":"myoferlin [Source:HGNC Symbol;Acc:HGNC:3656]","synonyms":"KIAA1207,FER1L3","biotype":"protein_coding","ncbi_id":"26509","summary":"Mutations in dysferlin, a protein associated with the plasma membrane, can cause muscle weakness that affects both proximal and distal muscles. The protein encoded by this gene is a type II membrane protein that is structurally similar to dysferlin. It is a member of the ferlin family and associates with both plasma and nuclear membranes. The protein contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. Two transcript variants encoding different isoforms have been found for this gene. Other possible variants have been detected, but their full-length nature has not been determined. [provided by RefSeq, Dec 2008]","start":93306429,"end":93482317,"strand":-1,"description":"myoferlin [Source:HGNC Symbol;Acc:HGNC:3656]"}, {"versioned_ensembl_gene_id":"ENSG00000242062.1","gene_symbol":"MARK2P6","gene_name":"microtubule affinity regulating kinase 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39797]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421500","summary":null,"start":128852112,"end":128853008,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39797]"}, {"versioned_ensembl_gene_id":"ENSG00000273204.1","gene_symbol":"AC104506.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100894928,"end":100895356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281332.1","gene_symbol":"AC018645.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32760279,"end":32762924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236603.2","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30485940,"end":30486590,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000272567.1","gene_symbol":"AC109347.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112272968,"end":112273316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142188.16","gene_symbol":"TMEM50B","gene_name":"transmembrane protein 50B [Source:HGNC Symbol;Acc:HGNC:1280]","synonyms":"C21orf4","biotype":"protein_coding","ncbi_id":"757","summary":null,"start":33432485,"end":33480011,"strand":-1,"description":"transmembrane protein 50B [Source:HGNC Symbol;Acc:HGNC:1280]"}, {"versioned_ensembl_gene_id":"ENSG00000257991.1","gene_symbol":"AC089984.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71835034,"end":71835396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130518.16","gene_symbol":"KIAA1683","gene_name":"KIAA1683 [Source:HGNC Symbol;Acc:HGNC:29350]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80726","summary":null,"start":18257097,"end":18274509,"strand":-1,"description":"KIAA1683 [Source:HGNC Symbol;Acc:HGNC:29350]"}, {"versioned_ensembl_gene_id":"ENSG00000249410.1","gene_symbol":"AK4P2","gene_name":"adenylate kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132104","summary":null,"start":55551885,"end":55552554,"strand":-1,"description":"adenylate kinase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39066]"}, {"versioned_ensembl_gene_id":"ENSG00000097096.8","gene_symbol":"SYDE2","gene_name":"synapse defective Rho GTPase homolog 2 [Source:HGNC Symbol;Acc:HGNC:25841]","synonyms":"FLJ13815","biotype":"protein_coding","ncbi_id":"84144","summary":null,"start":85156873,"end":85201046,"strand":-1,"description":"synapse defective Rho GTPase homolog 2 [Source:HGNC Symbol;Acc:HGNC:25841]"}, {"versioned_ensembl_gene_id":"ENSG00000237417.1","gene_symbol":"XRCC6P1","gene_name":"X-ray repair cross complementing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45183]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387703","summary":null,"start":93206857,"end":93209627,"strand":-1,"description":"X-ray repair cross complementing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45183]"}, {"versioned_ensembl_gene_id":"ENSG00000234107.1","gene_symbol":"TPT1P1","gene_name":"tumor protein, translationally-controlled 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16742]","synonyms":"TPT1P","biotype":"processed_pseudogene","ncbi_id":"100131268","summary":null,"start":31840341,"end":31840858,"strand":1,"description":"tumor protein, translationally-controlled 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16742]"}, {"versioned_ensembl_gene_id":"ENSG00000279318.1","gene_symbol":"AC008739.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20933201,"end":20935130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160055.19","gene_symbol":"TMEM234","gene_name":"transmembrane protein 234 [Source:HGNC Symbol;Acc:HGNC:28837]","synonyms":"RP4-622L5,FLJ90779,dJ622L5.7,C1orf91","biotype":"protein_coding","ncbi_id":"56063","summary":null,"start":32214472,"end":32222359,"strand":-1,"description":"transmembrane protein 234 [Source:HGNC Symbol;Acc:HGNC:28837]"}, {"versioned_ensembl_gene_id":"ENSG00000223642.7","gene_symbol":"AC008277.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159386367,"end":159404636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224152.1","gene_symbol":"AC009506.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159615296,"end":159617082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206495.12","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30315961,"end":30333218,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000214070.3","gene_symbol":"AC011999.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135897955,"end":135898978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228878.7","gene_symbol":"SEPT7-AS1","gene_name":"SEPT7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51153]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928545","summary":null,"start":35751856,"end":35800616,"strand":-1,"description":"SEPT7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51153]"}, {"versioned_ensembl_gene_id":"ENSG00000223944.1","gene_symbol":"AL353604.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37262739,"end":37325100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264745.1","gene_symbol":"TTC39C-AS1","gene_name":"TTC39C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51321]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724246","summary":null,"start":23994213,"end":24015339,"strand":-1,"description":"TTC39C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51321]"}, {"versioned_ensembl_gene_id":"ENSG00000120334.15","gene_symbol":"CENPL","gene_name":"centromere protein L [Source:HGNC Symbol;Acc:HGNC:17879]","synonyms":"dJ383J4.3,C1orf155,FLJ31044","biotype":"protein_coding","ncbi_id":"91687","summary":"CENPL is a subunit of a CENPH (MIM 605607)-CENPI (MIM 300065)-associated centromeric complex that targets CENPA (MIM 117139) to centromeres and is required for proper kinetochore function and mitotic progression (Okada et al., 2006) [PubMed 16622420].[supplied by OMIM, Mar 2008]","start":173799550,"end":173824720,"strand":-1,"description":"centromere protein L [Source:HGNC Symbol;Acc:HGNC:17879]"}, {"versioned_ensembl_gene_id":"ENSG00000205106.4","gene_symbol":"DKFZp779M0652","gene_name":"uncharacterized DKFZp779M0652 [Source:NCBI gene;Acc:374387]","synonyms":null,"biotype":"lincRNA","ncbi_id":"374387","summary":null,"start":45771432,"end":45772358,"strand":1,"description":"uncharacterized DKFZp779M0652 [Source:NCBI gene;Acc:374387]"}, {"versioned_ensembl_gene_id":"ENSG00000198081.10","gene_symbol":"ZBTB14","gene_name":"zinc finger and BTB domain containing 14 [Source:HGNC Symbol;Acc:HGNC:12860]","synonyms":"ZNF478,ZFP161","biotype":"protein_coding","ncbi_id":"7541","summary":null,"start":5289019,"end":5297053,"strand":-1,"description":"zinc finger and BTB domain containing 14 [Source:HGNC Symbol;Acc:HGNC:12860]"}, {"versioned_ensembl_gene_id":"ENSG00000273578.1","gene_symbol":"GU182359.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54754600,"end":54768961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228022.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"AB023051.1,NCRNA00149","biotype":"lincRNA","ncbi_id":"105375013","summary":null,"start":30766825,"end":30792250,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000261513.1","gene_symbol":"AC009097.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71723180,"end":71724230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155304.5","gene_symbol":"HSPA13","gene_name":"heat shock protein family A (Hsp70) member 13 [Source:HGNC Symbol;Acc:HGNC:11375]","synonyms":"STCH","biotype":"protein_coding","ncbi_id":"6782","summary":"The protein encoded by this gene is a member of the heat shock protein 70 family and is found associated with microsomes. Members of this protein family play a role in the processing of cytosolic and secretory proteins, as well as in the removal of denatured or incorrectly-folded proteins. The encoded protein contains an ATPase domain and has been shown to associate with a ubiquitin-like protein. [provided by RefSeq, Jul 2008]","start":14371115,"end":14383484,"strand":-1,"description":"heat shock protein family A (Hsp70) member 13 [Source:HGNC Symbol;Acc:HGNC:11375]"}, {"versioned_ensembl_gene_id":"ENSG00000133250.13","gene_symbol":"ZNF414","gene_name":"zinc finger protein 414 [Source:HGNC Symbol;Acc:HGNC:20630]","synonyms":"Zfp414,MGC15716","biotype":"protein_coding","ncbi_id":"84330","summary":null,"start":8509678,"end":8514164,"strand":-1,"description":"zinc finger protein 414 [Source:HGNC Symbol;Acc:HGNC:20630]"}, {"versioned_ensembl_gene_id":"ENSG00000267325.1","gene_symbol":"LINC01415","gene_name":"long intergenic non-protein coding RNA 1415 [Source:HGNC Symbol;Acc:HGNC:50709]","synonyms":"TCONS_00026208","biotype":"lincRNA","ncbi_id":"100132501","summary":null,"start":55776727,"end":55781721,"strand":-1,"description":"long intergenic non-protein coding RNA 1415 [Source:HGNC Symbol;Acc:HGNC:50709]"}, {"versioned_ensembl_gene_id":"ENSG00000264575.1","gene_symbol":"LINC00526","gene_name":"long intergenic non-protein coding RNA 526 [Source:HGNC Symbol;Acc:HGNC:28278]","synonyms":"MGC17515,HsT959,C18orf18","biotype":"lincRNA","ncbi_id":"147525","summary":null,"start":5236724,"end":5238598,"strand":-1,"description":"long intergenic non-protein coding RNA 526 [Source:HGNC Symbol;Acc:HGNC:28278]"}, {"versioned_ensembl_gene_id":"ENSG00000033122.18","gene_symbol":"LRRC7","gene_name":"leucine rich repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:18531]","synonyms":"KIAA1365,densin-180","biotype":"protein_coding","ncbi_id":"57554","summary":null,"start":69568398,"end":70151945,"strand":1,"description":"leucine rich repeat containing 7 [Source:HGNC Symbol;Acc:HGNC:18531]"}, {"versioned_ensembl_gene_id":"ENSG00000244101.1","gene_symbol":"HMGN1P10","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39353]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874438","summary":null,"start":136609050,"end":136609602,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39353]"}, {"versioned_ensembl_gene_id":"ENSG00000255192.5","gene_symbol":"NANOGP8","gene_name":"Nanog homeobox pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23106]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388112","summary":"This gene represents a transcribed retrogene of the Nanog homeobox gene. The putative encoded protein may participate in reprogramming of cancer cells. In vitro studies using a recombinant protein have shown that the protein localizes to the nucleus and can promote cell proliferation, similar to the Nanog protein. [provided by RefSeq, Sep 2017]","start":35084193,"end":35085110,"strand":-1,"description":"Nanog homeobox pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23106]"}, {"versioned_ensembl_gene_id":"ENSG00000257191.1","gene_symbol":"AC090709.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78960258,"end":79045644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243280.2","gene_symbol":"AC093663.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112171215,"end":112171527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259587.2","gene_symbol":"AC114546.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35008469,"end":35011191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162493.16","gene_symbol":"PDPN","gene_name":"podoplanin [Source:HGNC Symbol;Acc:HGNC:29602]","synonyms":"Gp38,aggrus,T1A-2,PA2.26,GP40","biotype":"protein_coding","ncbi_id":"10630","summary":"This gene encodes a type-I integral membrane glycoprotein with diverse distribution in human tissues. The physiological function of this protein may be related to its mucin-type character. The homologous protein in other species has been described as a differentiation antigen and influenza-virus receptor. The specific function of this protein has not been determined but it has been proposed as a marker of lung injury. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":13583465,"end":13617957,"strand":1,"description":"podoplanin [Source:HGNC Symbol;Acc:HGNC:29602]"}, {"versioned_ensembl_gene_id":"ENSG00000174721.9","gene_symbol":"FGFBP3","gene_name":"fibroblast growth factor binding protein 3 [Source:HGNC Symbol;Acc:HGNC:23428]","synonyms":"MGC39320,C10orf13","biotype":"protein_coding","ncbi_id":"143282","summary":null,"start":91906589,"end":91909483,"strand":-1,"description":"fibroblast growth factor binding protein 3 [Source:HGNC Symbol;Acc:HGNC:23428]"}, {"versioned_ensembl_gene_id":"ENSG00000259558.1","gene_symbol":"MESTP2","gene_name":"mesoderm specific transcript pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18208]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421572","summary":null,"start":60053204,"end":60054092,"strand":-1,"description":"mesoderm specific transcript pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18208]"}, {"versioned_ensembl_gene_id":"ENSG00000115850.9","gene_symbol":"LCT","gene_name":"lactase [Source:HGNC Symbol;Acc:HGNC:6530]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3938","summary":"The protein encoded by this gene belongs to the glycosyl hydrolase 1 family of proteins. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme is integral to the plasma membrane and has both phlorizin hydrolase activity and lactase activity. Mutations in this gene are associated with congenital lactase deficiency. Polymorphisms in this gene are associated with lactase persistence, in which intestinal lactase activity persists at childhood levels into adulthood. [provided by RefSeq, Jan 2016]","start":135787840,"end":135837180,"strand":-1,"description":"lactase [Source:HGNC Symbol;Acc:HGNC:6530]"}, {"versioned_ensembl_gene_id":"ENSG00000247728.2","gene_symbol":"AC091057.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30616998,"end":30625773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270016.1","gene_symbol":"AC026150.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30607695,"end":30608193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146535.13","gene_symbol":"GNA12","gene_name":"G protein subunit alpha 12 [Source:HGNC Symbol;Acc:HGNC:4380]","synonyms":"gep","biotype":"protein_coding","ncbi_id":"2768","summary":null,"start":2728112,"end":2844324,"strand":-1,"description":"G protein subunit alpha 12 [Source:HGNC Symbol;Acc:HGNC:4380]"}, {"versioned_ensembl_gene_id":"ENSG00000184220.11","gene_symbol":"CMSS1","gene_name":"cms1 ribosomal small subunit homolog (yeast) [Source:HGNC Symbol;Acc:HGNC:28666]","synonyms":"MGC4308,C3orf26","biotype":"protein_coding","ncbi_id":"84319","summary":null,"start":99817834,"end":100181732,"strand":1,"description":"cms1 ribosomal small subunit homolog (yeast) [Source:HGNC Symbol;Acc:HGNC:28666]"}, {"versioned_ensembl_gene_id":"ENSG00000266893.1","gene_symbol":"AC005394.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28491864,"end":28632728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122557.9","gene_symbol":"HERPUD2","gene_name":"HERPUD family member 2 [Source:HGNC Symbol;Acc:HGNC:21915]","synonyms":"FLJ22313","biotype":"protein_coding","ncbi_id":"64224","summary":null,"start":35632659,"end":35695571,"strand":-1,"description":"HERPUD family member 2 [Source:HGNC Symbol;Acc:HGNC:21915]"}, {"versioned_ensembl_gene_id":"ENSG00000211807.3","gene_symbol":"TRAV26-1","gene_name":"T-cell receptor alpha variable 26-1 [Source:HGNC Symbol;Acc:HGNC:12123]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28657","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22123318,"end":22124285,"strand":1,"description":"T-cell receptor alpha variable 26-1 [Source:HGNC Symbol;Acc:HGNC:12123]"}, {"versioned_ensembl_gene_id":"ENSG00000237664.1","gene_symbol":"LINC00316","gene_name":"long intergenic non-protein coding RNA 316 [Source:HGNC Symbol;Acc:HGNC:19723]","synonyms":"PRED59,NCRNA00316,C21orf111","biotype":"lincRNA","ncbi_id":"388830","summary":null,"start":45338590,"end":45341990,"strand":-1,"description":"long intergenic non-protein coding RNA 316 [Source:HGNC Symbol;Acc:HGNC:19723]"}, {"versioned_ensembl_gene_id":"ENSG00000253826.1","gene_symbol":"WBP1LP10","gene_name":"WW domain binding protein 1-like pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51470]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480326","summary":null,"start":75780,"end":76143,"strand":1,"description":"WW domain binding protein 1-like pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51470]"}, {"versioned_ensembl_gene_id":"ENSG00000161940.10","gene_symbol":"BCL6B","gene_name":"B-cell CLL/lymphoma 6B [Source:HGNC Symbol;Acc:HGNC:1002]","synonyms":"ZNF62,ZBTB28,BAZF","biotype":"protein_coding","ncbi_id":"255877","summary":null,"start":7023020,"end":7030290,"strand":1,"description":"B-cell CLL/lymphoma 6B [Source:HGNC Symbol;Acc:HGNC:1002]"}, {"versioned_ensembl_gene_id":"ENSG00000263253.1","gene_symbol":"AC092132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20208925,"end":20209525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271568.1","gene_symbol":"AC069304.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150603561,"end":150604644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257797.1","gene_symbol":"AC039056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42006132,"end":42010117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225371.1","gene_symbol":"CICP8","gene_name":"capicua transcriptional repressor pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37757]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442676","summary":null,"start":56362458,"end":56365270,"strand":1,"description":"capicua transcriptional repressor pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37757]"}, {"versioned_ensembl_gene_id":"ENSG00000161847.13","gene_symbol":"RAVER1","gene_name":"ribonucleoprotein, PTB binding 1 [Source:HGNC Symbol;Acc:HGNC:30296]","synonyms":"KIAA1978","biotype":"protein_coding","ncbi_id":"125950","summary":null,"start":10316212,"end":10333640,"strand":-1,"description":"ribonucleoprotein, PTB binding 1 [Source:HGNC Symbol;Acc:HGNC:30296]"}, {"versioned_ensembl_gene_id":"ENSG00000276605.1","gene_symbol":"AC027250.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54354168,"end":54355118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211804.3","gene_symbol":"TRDV1","gene_name":"T-cell receptor delta variable 1 [Source:HGNC Symbol;Acc:HGNC:12262]","synonyms":"hDV101S1","biotype":"TR_V_gene","ncbi_id":"28518","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22096032,"end":22096619,"strand":1,"description":"T-cell receptor delta variable 1 [Source:HGNC Symbol;Acc:HGNC:12262]"}, {"versioned_ensembl_gene_id":"ENSG00000185272.13","gene_symbol":"RBM11","gene_name":"RNA binding motif protein 11 [Source:HGNC Symbol;Acc:HGNC:9897]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54033","summary":null,"start":14216130,"end":14228372,"strand":1,"description":"RNA binding motif protein 11 [Source:HGNC Symbol;Acc:HGNC:9897]"}, {"versioned_ensembl_gene_id":"ENSG00000211800.3","gene_symbol":"TRAV20","gene_name":"T-cell receptor alpha variable 20 [Source:HGNC Symbol;Acc:HGNC:12117]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28663","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22040594,"end":22041153,"strand":1,"description":"T-cell receptor alpha variable 20 [Source:HGNC Symbol;Acc:HGNC:12117]"}, {"versioned_ensembl_gene_id":"ENSG00000258705.2","gene_symbol":"AC245505.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22011910,"end":22014964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257225.1","gene_symbol":"AC079601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42459366,"end":42466128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230637.2","gene_symbol":"AL022324.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25327252,"end":25339975,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115241.10","gene_symbol":"PPM1G","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1G [Source:HGNC Symbol;Acc:HGNC:9278]","synonyms":"PP2Cgamma,PP2CG","biotype":"protein_coding","ncbi_id":"5496","summary":"The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. This phosphatase is found to be responsible for the dephosphorylation of Pre-mRNA splicing factors, which is important for the formation of functional spliceosome. Studies of a similar gene in mice suggested a role of this phosphatase in regulating cell cycle progression. [provided by RefSeq, Apr 2010]","start":27381194,"end":27409687,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1G [Source:HGNC Symbol;Acc:HGNC:9278]"}, {"versioned_ensembl_gene_id":"ENSG00000262714.1","gene_symbol":"AC007342.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53386944,"end":53389085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220875.1","gene_symbol":"HIST1H3PS1","gene_name":"histone cluster 1 H3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18982]","synonyms":"H3F3AP1,dJ45P21.6","biotype":"processed_pseudogene","ncbi_id":"100289545","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 6. [provided by RefSeq, Oct 2015]","start":26321876,"end":26322292,"strand":-1,"description":"histone cluster 1 H3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18982]"}, {"versioned_ensembl_gene_id":"ENSG00000231409.3","gene_symbol":"AC018868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34943080,"end":34943394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214720.4","gene_symbol":"KRT18P49","gene_name":"keratin 18 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:33419]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392516","summary":null,"start":107428630,"end":107429461,"strand":1,"description":"keratin 18 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:33419]"}, {"versioned_ensembl_gene_id":"ENSG00000232473.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30353364,"end":30354532,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000177947.13","gene_symbol":"ODF3","gene_name":"outer dense fiber of sperm tails 3 [Source:HGNC Symbol;Acc:HGNC:19905]","synonyms":"SHIPPO1,hSHIPPO,CT135","biotype":"protein_coding","ncbi_id":"113746","summary":"ODF3 is a component of sperm flagella outer dense fibers, which add stiffness, elastic recoil, and protection against shearing forces during sperm movement.[supplied by OMIM, Apr 2004]","start":196738,"end":200261,"strand":1,"description":"outer dense fiber of sperm tails 3 [Source:HGNC Symbol;Acc:HGNC:19905]"}, {"versioned_ensembl_gene_id":"ENSG00000248432.1","gene_symbol":"AC139718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111804418,"end":111809694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111300.9","gene_symbol":"NAA25","gene_name":"N(alpha)-acetyltransferase 25, NatB auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:25783]","synonyms":"FLJ13089,C12orf30","biotype":"protein_coding","ncbi_id":"80018","summary":"This gene encodes the auxiliary subunit of the heteromeric N-terminal acetyltransferase B complex. This complex acetylates methionine residues that are followed by acidic or asparagine residues.[provided by RefSeq, Mar 2010]","start":112026689,"end":112109022,"strand":-1,"description":"N(alpha)-acetyltransferase 25, NatB auxiliary subunit [Source:HGNC Symbol;Acc:HGNC:25783]"}, {"versioned_ensembl_gene_id":"ENSG00000163331.11","gene_symbol":"DAPL1","gene_name":"death associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:21490]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92196","summary":null,"start":158795317,"end":158862781,"strand":1,"description":"death associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:21490]"}, {"versioned_ensembl_gene_id":"ENSG00000231299.1","gene_symbol":"SEPT14P24","gene_name":"septin 14 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51710]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480345","summary":null,"start":56360362,"end":56360541,"strand":-1,"description":"septin 14 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:51710]"}, {"versioned_ensembl_gene_id":"ENSG00000226163.1","gene_symbol":"AL513185.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72501746,"end":72502956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263037.1","gene_symbol":"MTX1P1","gene_name":"metaxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7505]","synonyms":"MTXP,MTX1P","biotype":"unprocessed_pseudogene","ncbi_id":"4581","summary":null,"start":155246379,"end":155249729,"strand":1,"description":"metaxin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7505]"}, {"versioned_ensembl_gene_id":"ENSG00000276144.1","gene_symbol":"AC233309.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7115736,"end":7116486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240286.1","gene_symbol":"MEAF6P1","gene_name":"MYST/Esa1-associated factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874045","summary":null,"start":209178804,"end":209182018,"strand":1,"description":"MYST/Esa1-associated factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42660]"}, {"versioned_ensembl_gene_id":"ENSG00000261572.1","gene_symbol":"AC097639.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32236688,"end":32238578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067248.9","gene_symbol":"DHX29","gene_name":"DExH-box helicase 29 [Source:HGNC Symbol;Acc:HGNC:15815]","synonyms":"DDX29","biotype":"protein_coding","ncbi_id":"54505","summary":"This gene encodes a member of the DEAH (Asp-Glu-Ala-His) subfamily of proteins, part of the DEAD (Asp-Glu-Ala-Asp) box family of RNA helicases. The encoded protein functions in translation initiation, and is specifically required for ribosomal scanning across stable mRNA secondary structures during initiation codon selection. This protein may also play a role in sensing virally derived cytosolic nucleic acids. Knockdown of this gene results in reduced protein translation and impaired proliferation of cancer cells. [provided by RefSeq, Sep 2016]","start":55256245,"end":55307722,"strand":-1,"description":"DExH-box helicase 29 [Source:HGNC Symbol;Acc:HGNC:15815]"}, {"versioned_ensembl_gene_id":"ENSG00000266853.1","gene_symbol":"AC015688.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27612588,"end":27613251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163576.17","gene_symbol":"EFHB","gene_name":"EF-hand domain family member B [Source:HGNC Symbol;Acc:HGNC:26330]","synonyms":"FLJ25200,CFAP21","biotype":"protein_coding","ncbi_id":"151651","summary":null,"start":19879472,"end":19947025,"strand":-1,"description":"EF-hand domain family member B [Source:HGNC Symbol;Acc:HGNC:26330]"}, {"versioned_ensembl_gene_id":"ENSG00000218357.3","gene_symbol":"LINC01644","gene_name":"long intergenic non-protein coding RNA 1644 [Source:HGNC Symbol;Acc:HGNC:52431]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927722","summary":null,"start":47461299,"end":47487111,"strand":-1,"description":"long intergenic non-protein coding RNA 1644 [Source:HGNC Symbol;Acc:HGNC:52431]"}, {"versioned_ensembl_gene_id":"ENSG00000225323.1","gene_symbol":"Z84721.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":168679,"end":169334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227949.1","gene_symbol":"CYCSP46","gene_name":"cytochrome c, somatic pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:23941]","synonyms":"HCP47,HCP46","biotype":"processed_pseudogene","ncbi_id":"286550","summary":null,"start":14941547,"end":14941750,"strand":-1,"description":"cytochrome c, somatic pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:23941]"}, {"versioned_ensembl_gene_id":"ENSG00000179144.4","gene_symbol":"GIMAP7","gene_name":"GTPase, IMAP family member 7 [Source:HGNC Symbol;Acc:HGNC:22404]","synonyms":"MGC27027,IAN7","biotype":"protein_coding","ncbi_id":"168537","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]","start":150514830,"end":150521073,"strand":1,"description":"GTPase, IMAP family member 7 [Source:HGNC Symbol;Acc:HGNC:22404]"}, {"versioned_ensembl_gene_id":"ENSG00000281121.1","gene_symbol":"AC244216.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13292116,"end":13294207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277775.1","gene_symbol":"HIST1H3F","gene_name":"histone cluster 1 H3 family member f [Source:HGNC Symbol;Acc:HGNC:4773]","synonyms":"H3FI,H3/i","biotype":"protein_coding","ncbi_id":"8968","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26250195,"end":26250605,"strand":-1,"description":"histone cluster 1 H3 family member f [Source:HGNC Symbol;Acc:HGNC:4773]"}, {"versioned_ensembl_gene_id":"ENSG00000254235.5","gene_symbol":"AC022784.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9249417,"end":9413714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235361.1","gene_symbol":"AC016292.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1181893,"end":1185086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085491.15","gene_symbol":"SLC25A24","gene_name":"solute carrier family 25 member 24 [Source:HGNC Symbol;Acc:HGNC:20662]","synonyms":"DKFZp586G0123,APC1","biotype":"protein_coding","ncbi_id":"29957","summary":"This gene encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":108134036,"end":108200849,"strand":-1,"description":"solute carrier family 25 member 24 [Source:HGNC Symbol;Acc:HGNC:20662]"}, {"versioned_ensembl_gene_id":"ENSG00000162975.4","gene_symbol":"KCNF1","gene_name":"potassium voltage-gated channel modifier subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:6246]","synonyms":"Kv5.1,kH1,KCNF,IK8","biotype":"protein_coding","ncbi_id":"3754","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily F. This gene is intronless and expressed in all tissues tested, including the heart, skeletal muscle, brain, kidney, and pancreas. [provided by RefSeq, Jul 2008]","start":10911937,"end":10914225,"strand":1,"description":"potassium voltage-gated channel modifier subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:6246]"}, {"versioned_ensembl_gene_id":"ENSG00000099256.18","gene_symbol":"PRTFDC1","gene_name":"phosphoribosyl transferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23333]","synonyms":"HHGP","biotype":"protein_coding","ncbi_id":"56952","summary":null,"start":24848607,"end":24952604,"strand":-1,"description":"phosphoribosyl transferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23333]"}, {"versioned_ensembl_gene_id":"ENSG00000228667.1","gene_symbol":"AL157385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24867645,"end":24868190,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226762.1","gene_symbol":"AL451164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3240371,"end":3257210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185894.8","gene_symbol":"BPY2C","gene_name":"basic charge, Y-linked, 2C [Source:HGNC Symbol;Acc:HGNC:18225]","synonyms":"VCY2C","biotype":"protein_coding","ncbi_id":"442868","summary":"This gene is located in the nonrecombining portion of the Y chromosome, and expressed specifically in testis. The encoded protein interacts with ubiquitin protein ligase E3A and may be involved in male germ cell development and male infertility. Three nearly identical copies of this gene exist on chromosome Y; two copies are part of a palindromic region. This record represents the more telomeric copy within the palindrome. [provided by RefSeq, Jul 2008]","start":25030901,"end":25062548,"strand":-1,"description":"basic charge, Y-linked, 2C [Source:HGNC Symbol;Acc:HGNC:18225]"}, {"versioned_ensembl_gene_id":"ENSG00000235140.1","gene_symbol":"AC026391.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59589150,"end":59611248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173272.15","gene_symbol":"MZT2A","gene_name":"mitotic spindle organizing protein 2A [Source:HGNC Symbol;Acc:HGNC:33187]","synonyms":"MOZART2A,FAM128A","biotype":"protein_coding","ncbi_id":"653784","summary":null,"start":131464900,"end":131492743,"strand":-1,"description":"mitotic spindle organizing protein 2A [Source:HGNC Symbol;Acc:HGNC:33187]"}, {"versioned_ensembl_gene_id":"ENSG00000260909.1","gene_symbol":"AC012186.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46649126,"end":46649849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278992.1","gene_symbol":"AC012048.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":76270206,"end":76270800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261537.1","gene_symbol":"AC027279.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":78994345,"end":79004730,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215000.4","gene_symbol":"AL034403.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109341813,"end":109342697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243844.1","gene_symbol":"AC069181.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29632091,"end":29632644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228352.2","gene_symbol":"AL354989.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34084332,"end":34096225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125533.5","gene_symbol":"BHLHE23","gene_name":"basic helix-loop-helix family member e23 [Source:HGNC Symbol;Acc:HGNC:16093]","synonyms":"bHLHe23,BHLHB4,Beta4,bA305P22.3","biotype":"protein_coding","ncbi_id":"128408","summary":"This gene encodes a member of the basic helix-loop-helix transcription factor family. Members of this family contain two highly conserved and functionally distinct domains: the basic domain targets sequence-specific DNA binding, while the helix-loop-helix domain facilitates protein interaction. Studies of a related gene in mouse suggest that the encoded protein may function as a transcriptional repressor in the pancreas and brain, and that it is required for normal retinal function. [provided by RefSeq, May 2013]","start":63005927,"end":63007035,"strand":-1,"description":"basic helix-loop-helix family member e23 [Source:HGNC Symbol;Acc:HGNC:16093]"}, {"versioned_ensembl_gene_id":"ENSG00000281801.1","gene_symbol":"KRTAP5-AS1","gene_name":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338651","summary":null,"start":1577063,"end":1604894,"strand":1,"description":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]"}, {"versioned_ensembl_gene_id":"ENSG00000235886.1","gene_symbol":"AC006055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43778961,"end":43779982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272512.1","gene_symbol":"AL645608.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":995966,"end":998051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136689.18","gene_symbol":"IL1RN","gene_name":"interleukin 1 receptor antagonist [Source:HGNC Symbol;Acc:HGNC:6000]","synonyms":"IL-1RN,ICIL-1RA,MGC10430,IRAP,IL1RA,IL1F3","biotype":"protein_coding","ncbi_id":"3557","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This protein inhibits the activities of interleukin 1, alpha (IL1A) and interleukin 1, beta (IL1B), and modulates a variety of interleukin 1 related immune and inflammatory responses, particularly in the acute phase of infection and inflammation. This gene and five other closely related cytokine genes form a gene cluster spanning approximately 400 kb on chromosome 2. A polymorphism of this gene is reported to be associated with increased risk of osteoporotic fractures and gastric cancer. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Aug 2020]","start":113107214,"end":113134016,"strand":1,"description":"interleukin 1 receptor antagonist [Source:HGNC Symbol;Acc:HGNC:6000]"}, {"versioned_ensembl_gene_id":"ENSG00000267301.1","gene_symbol":"RPL23AP77","gene_name":"ribosomal protein L23a pseudogene 77 [Source:HGNC Symbol;Acc:HGNC:36354]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728538","summary":null,"start":23709825,"end":23710287,"strand":-1,"description":"ribosomal protein L23a pseudogene 77 [Source:HGNC Symbol;Acc:HGNC:36354]"}, {"versioned_ensembl_gene_id":"ENSG00000164483.16","gene_symbol":"SAMD3","gene_name":"sterile alpha motif domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21574]","synonyms":"FLJ34032,bA73O6.2","biotype":"protein_coding","ncbi_id":"154075","summary":null,"start":130144315,"end":130365425,"strand":-1,"description":"sterile alpha motif domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21574]"}, {"versioned_ensembl_gene_id":"ENSG00000225549.3","gene_symbol":"AL359634.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":118757518,"end":118783420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250933.1","gene_symbol":"GAPDHP66","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:4144]","synonyms":"GAPDL11,GAPDHL11","biotype":"processed_pseudogene","ncbi_id":"645256","summary":null,"start":3977649,"end":3978615,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:4144]"}, {"versioned_ensembl_gene_id":"ENSG00000271105.1","gene_symbol":"AC133552.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25069570,"end":25070109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262155.1","gene_symbol":"LINC02175","gene_name":"long intergenic non-protein coding RNA 2175 [Source:HGNC Symbol;Acc:HGNC:27550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283887","summary":null,"start":25066937,"end":25068943,"strand":1,"description":"long intergenic non-protein coding RNA 2175 [Source:HGNC Symbol;Acc:HGNC:27550]"}, {"versioned_ensembl_gene_id":"ENSG00000156234.7","gene_symbol":"CXCL13","gene_name":"C-X-C motif chemokine ligand 13 [Source:HGNC Symbol;Acc:HGNC:10639]","synonyms":"SCYB13,BLR1L,BLC,BCA-1,ANGIE2,ANGIE","biotype":"protein_coding","ncbi_id":"10563","summary":"B lymphocyte chemoattractant, independently cloned and named Angie, is an antimicrobial peptide and CXC chemokine strongly expressed in the follicles of the spleen, lymph nodes, and Peyer's patches. It preferentially promotes the migration of B lymphocytes (compared to T cells and macrophages), apparently by stimulating calcium influx into, and chemotaxis of, cells expressing Burkitt's lymphoma receptor 1 (BLR-1). It may therefore function in the homing of B lymphocytes to follicles. [provided by RefSeq, Oct 2014]","start":77511753,"end":77611834,"strand":1,"description":"C-X-C motif chemokine ligand 13 [Source:HGNC Symbol;Acc:HGNC:10639]"}, {"versioned_ensembl_gene_id":"ENSG00000204364.10","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31959563,"end":31985058,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000119801.12","gene_symbol":"YPEL5","gene_name":"yippee like 5 [Source:HGNC Symbol;Acc:HGNC:18329]","synonyms":"CGI-127","biotype":"protein_coding","ncbi_id":"51646","summary":null,"start":30146941,"end":30160533,"strand":1,"description":"yippee like 5 [Source:HGNC Symbol;Acc:HGNC:18329]"}, {"versioned_ensembl_gene_id":"ENSG00000227070.1","gene_symbol":"AC104170.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51518309,"end":51561629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281642.1","gene_symbol":"AC127032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45835461,"end":45836529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068985.4","gene_symbol":"PAGE1","gene_name":"PAGE family member 1 [Source:HGNC Symbol;Acc:HGNC:4107]","synonyms":"PAGE-1,GAGEB1,GAGE-9,CT16.3","biotype":"protein_coding","ncbi_id":"8712","summary":"This gene belongs to a family of genes that are expressed in a variety of tumors but not in normal tissues, except for the testis. Unlike the other gene family members, this gene does not encode an antigenic peptide. Nothing is presently known about the function of this protein. [provided by RefSeq, Jul 2008]","start":49687450,"end":49695993,"strand":-1,"description":"PAGE family member 1 [Source:HGNC Symbol;Acc:HGNC:4107]"}, {"versioned_ensembl_gene_id":"ENSG00000235688.2","gene_symbol":"AC116614.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":949627,"end":950274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227014.5","gene_symbol":"AC007285.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29988600,"end":30025660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241735.1","gene_symbol":"FABP5P3","gene_name":"fatty acid binding protein 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22573]","synonyms":"TCAG_1781704,FABP5L3","biotype":"transcribed_processed_pseudogene","ncbi_id":"220832","summary":null,"start":152436895,"end":152443187,"strand":1,"description":"fatty acid binding protein 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22573]"}, {"versioned_ensembl_gene_id":"ENSG00000159387.7","gene_symbol":"IRX6","gene_name":"iroquois homeobox 6 [Source:HGNC Symbol;Acc:HGNC:14675]","synonyms":"IRX7,IRX-3","biotype":"protein_coding","ncbi_id":"79190","summary":null,"start":55323760,"end":55330760,"strand":1,"description":"iroquois homeobox 6 [Source:HGNC Symbol;Acc:HGNC:14675]"}, {"versioned_ensembl_gene_id":"ENSG00000258284.1","gene_symbol":"POLR2KP1","gene_name":"RNA polymerase II subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42650]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874515","summary":null,"start":49594091,"end":49594258,"strand":1,"description":"RNA polymerase II subunit K pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42650]"}, {"versioned_ensembl_gene_id":"ENSG00000224697.1","gene_symbol":"NEFMP1","gene_name":"neurofilament medium pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420737","summary":null,"start":54599678,"end":54600683,"strand":1,"description":"neurofilament medium pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45030]"}, {"versioned_ensembl_gene_id":"ENSG00000225519.1","gene_symbol":"AL365434.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90994620,"end":91006390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233057.1","gene_symbol":"EEF1A1P14","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:3197]","synonyms":"EEF1AL12","biotype":"processed_pseudogene","ncbi_id":"647167","summary":null,"start":194188967,"end":194190342,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:3197]"}, {"versioned_ensembl_gene_id":"ENSG00000270865.1","gene_symbol":"RPL12P48","gene_name":"ribosomal protein L12 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:51940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101926938","summary":null,"start":37983070,"end":37983373,"strand":1,"description":"ribosomal protein L12 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:51940]"}, {"versioned_ensembl_gene_id":"ENSG00000138032.20","gene_symbol":"PPM1B","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1B [Source:HGNC Symbol;Acc:HGNC:9276]","synonyms":"PPC2BETAX,PP2CBETA,PP2CB","biotype":"protein_coding","ncbi_id":"5495","summary":"The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. This phosphatase has been shown to dephosphorylate cyclin-dependent kinases (CDKs), and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to cause cell-growth arrest or cell death. Alternative splicing results in multiple transcript variants encoding different isoforms. Additional transcript variants have been described, but currently do not represent full-length sequences. [provided by RefSeq, Jul 2008]","start":44167969,"end":44244384,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1B [Source:HGNC Symbol;Acc:HGNC:9276]"}, {"versioned_ensembl_gene_id":"ENSG00000223800.1","gene_symbol":"AL355314.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55468327,"end":55469222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166016.5","gene_symbol":"ABTB2","gene_name":"ankyrin repeat and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23842]","synonyms":"DKFZP586C1619,BTBD22,ABTB2A","biotype":"protein_coding","ncbi_id":"25841","summary":null,"start":34150988,"end":34358008,"strand":-1,"description":"ankyrin repeat and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23842]"}, {"versioned_ensembl_gene_id":"ENSG00000182586.8","gene_symbol":"LINC00334","gene_name":"long intergenic non-protein coding RNA 334 [Source:HGNC Symbol;Acc:HGNC:16425]","synonyms":"NCRNA00334,C21orf89","biotype":"lincRNA","ncbi_id":"114042","summary":null,"start":45234340,"end":45264548,"strand":1,"description":"long intergenic non-protein coding RNA 334 [Source:HGNC Symbol;Acc:HGNC:16425]"}, {"versioned_ensembl_gene_id":"ENSG00000227391.1","gene_symbol":"SALL1P1","gene_name":"spalt like transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10525]","synonyms":"SALL1P","biotype":"processed_pseudogene","ncbi_id":"139163","summary":null,"start":49664844,"end":49668680,"strand":-1,"description":"spalt like transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10525]"}, {"versioned_ensembl_gene_id":"ENSG00000281048.2","gene_symbol":"AC114936.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177954877,"end":177967034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281100.1","gene_symbol":"AC105749.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36823151,"end":36825158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270618.1","gene_symbol":"AL160237.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23767662,"end":23768998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281513.1","gene_symbol":"AC114936.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177970078,"end":177970531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236362.8","gene_symbol":"GAGE12F","gene_name":"G antigen 12F [Source:HGNC Symbol;Acc:HGNC:31906]","synonyms":"OTTHUMG00000024147","biotype":"protein_coding","ncbi_id":"100008586","summary":null,"start":49551278,"end":49568218,"strand":1,"description":"G antigen 12F [Source:HGNC Symbol;Acc:HGNC:31906]"}, {"versioned_ensembl_gene_id":"ENSG00000246130.1","gene_symbol":"AC107959.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23068229,"end":23083619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282665.1","gene_symbol":"ERICH1","gene_name":"glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:27234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"157697","summary":null,"start":731140,"end":738106,"strand":-1,"description":"glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:27234]"}, {"versioned_ensembl_gene_id":"ENSG00000215269.5","gene_symbol":"GAGE12G","gene_name":"G antigen 12G [Source:HGNC Symbol;Acc:HGNC:31907]","synonyms":"OTTHUMG00000024148","biotype":"protein_coding","ncbi_id":"645073","summary":null,"start":49570434,"end":49577754,"strand":1,"description":"G antigen 12G [Source:HGNC Symbol;Acc:HGNC:31907]"}, {"versioned_ensembl_gene_id":"ENSG00000119537.15","gene_symbol":"KDSR","gene_name":"3-ketodihydrosphingosine reductase [Source:HGNC Symbol;Acc:HGNC:4021]","synonyms":"SDR35C1,FVT1,DHSR","biotype":"protein_coding","ncbi_id":"2531","summary":"The protein encoded by this gene catalyzes the reduction of 3-ketodihydrosphingosine to dihydrosphingosine. The putative active site residues of the encoded protein are found on the cytosolic side of the endoplasmic reticulum membrane. A chromosomal rearrangement involving this gene is a cause of follicular lymphoma, also known as type II chronic lymphatic leukemia. The mutation of a conserved residue in the bovine ortholog causes spinal muscular atrophy. [provided by RefSeq, Jul 2008]","start":63327726,"end":63367510,"strand":-1,"description":"3-ketodihydrosphingosine reductase [Source:HGNC Symbol;Acc:HGNC:4021]"}, {"versioned_ensembl_gene_id":"ENSG00000227776.1","gene_symbol":"AKR1D1P1","gene_name":"aldo-keto reductase family 1 member D1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11288]","synonyms":"SRD5BP1,AKR1D1P","biotype":"processed_pseudogene","ncbi_id":"80701","summary":null,"start":167519536,"end":167520586,"strand":1,"description":"aldo-keto reductase family 1 member D1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11288]"}, {"versioned_ensembl_gene_id":"ENSG00000259899.1","gene_symbol":"AC010333.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12560756,"end":12611044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256081.2","gene_symbol":"AC243972.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21585290,"end":21586280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268785.1","gene_symbol":"RPL7P50","gene_name":"ribosomal protein L7 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35816]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729449","summary":null,"start":6593329,"end":6594055,"strand":1,"description":"ribosomal protein L7 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35816]"}, {"versioned_ensembl_gene_id":"ENSG00000283258.1","gene_symbol":"AC007491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54628963,"end":54657662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283304.1","gene_symbol":"LINC02183","gene_name":"long intergenic non-protein coding RNA 2183 [Source:HGNC Symbol;Acc:HGNC:53045]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371273","summary":null,"start":54542808,"end":54559100,"strand":-1,"description":"long intergenic non-protein coding RNA 2183 [Source:HGNC Symbol;Acc:HGNC:53045]"}, {"versioned_ensembl_gene_id":"ENSG00000169208.2","gene_symbol":"OR10G3","gene_name":"olfactory receptor family 10 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:8171]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26533","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21568520,"end":21580076,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:8171]"}, {"versioned_ensembl_gene_id":"ENSG00000227513.1","gene_symbol":"AC114755.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106344566,"end":106345433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229308.1","gene_symbol":"AC010737.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4036497,"end":4100320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230353.5","gene_symbol":"AC114755.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106288803,"end":106289053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128710.5","gene_symbol":"HOXD10","gene_name":"homeobox D10 [Source:HGNC Symbol;Acc:HGNC:5133]","synonyms":"HOX4,HOX4D","biotype":"protein_coding","ncbi_id":"3236","summary":"This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as \"rocker-bottom foot\" deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease. [provided by RefSeq, Jul 2008]","start":176108790,"end":176119942,"strand":1,"description":"homeobox D10 [Source:HGNC Symbol;Acc:HGNC:5133]"}, {"versioned_ensembl_gene_id":"ENSG00000275322.1","gene_symbol":"AC103746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96342953,"end":96345651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240108.1","gene_symbol":"NCOR1P1","gene_name":"nuclear receptor corepressor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16724]","synonyms":"C20orf191,bB329D4.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"149934","summary":null,"start":26103416,"end":26114028,"strand":-1,"description":"nuclear receptor corepressor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16724]"}, {"versioned_ensembl_gene_id":"ENSG00000214575.9","gene_symbol":"CPEB1","gene_name":"cytoplasmic polyadenylation element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21744]","synonyms":"FLJ13203,CPEB","biotype":"protein_coding","ncbi_id":"64506","summary":"This gene encodes a member of the cytoplasmic polyadenylation element binding protein family. This highly conserved protein binds to a specific RNA sequence, called the cytoplasmic polyadenylation element, found in the 3' untranslated region of some mRNAs. The encoded protein functions in both the cytoplasm and the nucleus. It is involved in the regulation of mRNA translation, as well as processing of the 3' untranslated region, and may play a role in cell proliferation and tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":82543201,"end":82648861,"strand":-1,"description":"cytoplasmic polyadenylation element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21744]"}, {"versioned_ensembl_gene_id":"ENSG00000171385.9","gene_symbol":"KCND3","gene_name":"potassium voltage-gated channel subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:6239]","synonyms":"SCA22,SCA19,Kv4.3,KSHIVB","biotype":"protein_coding","ncbi_id":"3752","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shal-related subfamily, members of which form voltage-activated A-type potassium ion channels and are prominent in the repolarization phase of the action potential. This member includes two isoforms with different sizes, which are encoded by alternatively spliced transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":111770662,"end":111989155,"strand":-1,"description":"potassium voltage-gated channel subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:6239]"}, {"versioned_ensembl_gene_id":"ENSG00000239873.2","gene_symbol":"GAPDHP27","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37779]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401960","summary":null,"start":119558755,"end":119559774,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:37779]"}, {"versioned_ensembl_gene_id":"ENSG00000125804.13","gene_symbol":"FAM182A","gene_name":"family with sequence similarity 182 member A [Source:HGNC Symbol;Acc:HGNC:16222]","synonyms":"C20orf91A,C20orf91,bB329D4.1","biotype":"processed_transcript","ncbi_id":"284800","summary":null,"start":26054655,"end":26086917,"strand":1,"description":"family with sequence similarity 182 member A [Source:HGNC Symbol;Acc:HGNC:16222]"}, {"versioned_ensembl_gene_id":"ENSG00000056277.15","gene_symbol":"ZNF280C","gene_name":"zinc finger protein 280C [Source:HGNC Symbol;Acc:HGNC:25955]","synonyms":"ZNF633,SUHW3,FLJ20095","biotype":"protein_coding","ncbi_id":"55609","summary":"This gene encodes a member of the zinc finger domain-containing protein family. This family member contains multiple Cys2-His2(C2H2)-type zinc finger domains, the most common type of zinc finger domain that self-folds to form a beta-beta-alpha structure that binds a zinc ion. [provided by RefSeq, Aug 2011]","start":130202711,"end":130268899,"strand":-1,"description":"zinc finger protein 280C [Source:HGNC Symbol;Acc:HGNC:25955]"}, {"versioned_ensembl_gene_id":"ENSG00000183971.6","gene_symbol":"NPW","gene_name":"neuropeptide W [Source:HGNC Symbol;Acc:HGNC:30509]","synonyms":"PPL8","biotype":"protein_coding","ncbi_id":"283869","summary":"The product of this gene is processed into 23- and 30-amino acid neuropeptides that bind and activate two G-protein coupled receptors in the central nervous system. The neuropeptides have been shown to enhance cortisol secretion from adrenal cells through the adenylate cyclase/protein kinase A signaling cascade. The preproprotein is translated using a non-AUG initiation codon that is inferred from analyses of the mouse ortholog. [provided by RefSeq, Jul 2008]","start":2009926,"end":2020755,"strand":1,"description":"neuropeptide W [Source:HGNC Symbol;Acc:HGNC:30509]"}, {"versioned_ensembl_gene_id":"ENSG00000218410.1","gene_symbol":"AC012078.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3851224,"end":3852869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176444.18","gene_symbol":"CLK2","gene_name":"CDC like kinase 2 [Source:HGNC Symbol;Acc:HGNC:2069]","synonyms":"clk2","biotype":"protein_coding","ncbi_id":"1196","summary":"This gene encodes a dual specificity protein kinase that phosphorylates serine/threonine and tyrosine-containing substrates. Activity of this protein regulates serine- and arginine-rich (SR) proteins of the spliceosomal complex, thereby influencing alternative transcript splicing. Chromosomal translocations have been characterized between this locus and the PAFAH1B3 (platelet-activating factor acetylhydrolase 1b, catalytic subunit 3 (29kDa)) gene on chromosome 19, resulting in the production of a fusion protein. Note that this gene is distinct from the TELO2 gene (GeneID:9894), which shares the CLK2 alias, but encodes a protein that is involved in telomere length regulation. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":155262868,"end":155278491,"strand":-1,"description":"CDC like kinase 2 [Source:HGNC Symbol;Acc:HGNC:2069]"}, {"versioned_ensembl_gene_id":"ENSG00000280159.1","gene_symbol":"AC016583.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":54643557,"end":54645987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236073.2","gene_symbol":"AL627311.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21073639,"end":21073753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234538.1","gene_symbol":"ZNF114P1","gene_name":"zinc finger protein 114 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23771]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132509","summary":null,"start":13839118,"end":13839409,"strand":1,"description":"zinc finger protein 114 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23771]"}, {"versioned_ensembl_gene_id":"ENSG00000215562.2","gene_symbol":"CNN2P7","gene_name":"calponin 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39532]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391266","summary":null,"start":13826696,"end":13827627,"strand":1,"description":"calponin 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39532]"}, {"versioned_ensembl_gene_id":"ENSG00000232545.1","gene_symbol":"AC253536.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24101689,"end":24103354,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156787.16","gene_symbol":"TBC1D31","gene_name":"TBC1 domain family member 31 [Source:HGNC Symbol;Acc:HGNC:30888]","synonyms":"Gm85,WDR67,MGC21654","biotype":"protein_coding","ncbi_id":"93594","summary":null,"start":123041968,"end":123152153,"strand":1,"description":"TBC1 domain family member 31 [Source:HGNC Symbol;Acc:HGNC:30888]"}, {"versioned_ensembl_gene_id":"ENSG00000102908.20","gene_symbol":"NFAT5","gene_name":"nuclear factor of activated T-cells 5 [Source:HGNC Symbol;Acc:HGNC:7774]","synonyms":"TONEBP,OREBP,NFATZ,NFATL1,NF-AT5,KIAA0827","biotype":"protein_coding","ncbi_id":"10725","summary":"The product of this gene is a member of the nuclear factors of activated T cells family of transcription factors. Proteins belonging to this family play a central role in inducible gene transcription during the immune response. This protein regulates gene expression induced by osmotic stress in mammalian cells. Unlike monomeric members of this protein family, this protein exists as a homodimer and forms stable dimers with DNA elements. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":69565094,"end":69704666,"strand":1,"description":"nuclear factor of activated T-cells 5 [Source:HGNC Symbol;Acc:HGNC:7774]"}, {"versioned_ensembl_gene_id":"ENSG00000281062.2","gene_symbol":"AC240720.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":198106449,"end":198108214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281503.1","gene_symbol":"AC240720.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":198116056,"end":198117113,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205444.2","gene_symbol":"AL034376.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4610656,"end":4611304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128789.20","gene_symbol":"PSMG2","gene_name":"proteasome assembly chaperone 2 [Source:HGNC Symbol;Acc:HGNC:24929]","synonyms":"TNFSF5IP1,PAC2,MGC15092,MDS003,HsT1707,HCCA3,CLAST3","biotype":"protein_coding","ncbi_id":"56984","summary":null,"start":12658043,"end":12725740,"strand":1,"description":"proteasome assembly chaperone 2 [Source:HGNC Symbol;Acc:HGNC:24929]"}, {"versioned_ensembl_gene_id":"ENSG00000253958.1","gene_symbol":"CLDN23","gene_name":"claudin 23 [Source:HGNC Symbol;Acc:HGNC:17591]","synonyms":"CLDNL","biotype":"protein_coding","ncbi_id":"137075","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is expressed in germinal center B-cells, placenta and stomach as well as in colon tumor. This gene is down-regulated in intestinal type gastric cancer. [provided by RefSeq, Aug 2010]","start":8701938,"end":8704106,"strand":1,"description":"claudin 23 [Source:HGNC Symbol;Acc:HGNC:17591]"}, {"versioned_ensembl_gene_id":"ENSG00000253343.1","gene_symbol":"AC114550.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8555738,"end":8560965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279721.1","gene_symbol":"AC018737.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":121688203,"end":121689714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140350.15","gene_symbol":"ANP32A","gene_name":"acidic nuclear phosphoprotein 32 family member A [Source:HGNC Symbol;Acc:HGNC:13233]","synonyms":"mapmodulin,MAPM,LANP,I1PP2A,C15orf1,PP32,PHAPI","biotype":"protein_coding","ncbi_id":"8125","summary":null,"start":68778535,"end":68820897,"strand":-1,"description":"acidic nuclear phosphoprotein 32 family member A [Source:HGNC Symbol;Acc:HGNC:13233]"}, {"versioned_ensembl_gene_id":"ENSG00000282875.1","gene_symbol":"BX322534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133778258,"end":133778498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277651.1","gene_symbol":"AL391261.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65986967,"end":65987447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235069.2","gene_symbol":"AL627082.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26647447,"end":26647681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171735.18","gene_symbol":"CAMTA1","gene_name":"calmodulin binding transcription activator 1 [Source:HGNC Symbol;Acc:HGNC:18806]","synonyms":"KIAA0833","biotype":"protein_coding","ncbi_id":"23261","summary":"The protein encoded by this gene contains a CG1 DNA-binding domain, a transcription factor immunoglobulin domain, ankyrin repeats, and calmodulin-binding IQ motifs. The encoded protein is thought to be a transcription factor and may be a tumor suppressor. However, a translocation event is sometimes observed between this gene and the WWTR1 gene, with the resulting WWTR1-CAMTA1 oncoprotein leading to epithelioid hemangioendothelioma, a malignant vascular cancer. [provided by RefSeq, Mar 2017]","start":6785324,"end":7769706,"strand":1,"description":"calmodulin binding transcription activator 1 [Source:HGNC Symbol;Acc:HGNC:18806]"}, {"versioned_ensembl_gene_id":"ENSG00000253130.1","gene_symbol":"AC114550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8561391,"end":8569688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237978.5","gene_symbol":"KCNMB2-AS1","gene_name":"KCNMB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51409]","synonyms":"RP11-385J1.2","biotype":"antisense_RNA","ncbi_id":"104797538","summary":null,"start":178526505,"end":178860405,"strand":-1,"description":"KCNMB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51409]"}, {"versioned_ensembl_gene_id":"ENSG00000233896.1","gene_symbol":"PDYN-AS1","gene_name":"PDYN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53462]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"727993","summary":null,"start":1947246,"end":2007517,"strand":1,"description":"PDYN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53462]"}, {"versioned_ensembl_gene_id":"ENSG00000173231.6","gene_symbol":"TERF1P1","gene_name":"telomeric repeat binding factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16733]","synonyms":"TERF1P","biotype":"processed_pseudogene","ncbi_id":"348567","summary":null,"start":13776086,"end":13777266,"strand":1,"description":"telomeric repeat binding factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16733]"}, {"versioned_ensembl_gene_id":"ENSG00000223941.5","gene_symbol":"LINC01014","gene_name":"long intergenic non-protein coding RNA 1014 [Source:HGNC Symbol;Acc:HGNC:41353]","synonyms":"KCNMB2-IT1","biotype":"sense_intronic","ncbi_id":"100874330","summary":null,"start":178419201,"end":178457309,"strand":1,"description":"long intergenic non-protein coding RNA 1014 [Source:HGNC Symbol;Acc:HGNC:41353]"}, {"versioned_ensembl_gene_id":"ENSG00000224922.1","gene_symbol":"AL050303.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13769932,"end":13771740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229231.1","gene_symbol":"FEM1AP1","gene_name":"fem-1 homolog A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17219]","synonyms":"FEM1DP","biotype":"processed_pseudogene","ncbi_id":"441957","summary":null,"start":13762338,"end":13764332,"strand":1,"description":"fem-1 homolog A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17219]"}, {"versioned_ensembl_gene_id":"ENSG00000213096.10","gene_symbol":"ZNF254","gene_name":"zinc finger protein 254 [Source:HGNC Symbol;Acc:HGNC:13047]","synonyms":"HD-ZNF1,BMZF-5,ZNF91L,ZNF539","biotype":"protein_coding","ncbi_id":"9534","summary":"Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002]","start":24033405,"end":24129961,"strand":1,"description":"zinc finger protein 254 [Source:HGNC Symbol;Acc:HGNC:13047]"}, {"versioned_ensembl_gene_id":"ENSG00000233970.1","gene_symbol":"AC092159.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":692083,"end":693235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055609.17","gene_symbol":"KMT2C","gene_name":"lysine methyltransferase 2C [Source:HGNC Symbol;Acc:HGNC:13726]","synonyms":"MLL3,KIAA1506,HALR","biotype":"protein_coding","ncbi_id":"58508","summary":"This gene is a member of the myeloid/lymphoid or mixed-lineage leukemia (MLL) family and encodes a nuclear protein with an AT hook DNA-binding domain, a DHHC-type zinc finger, six PHD-type zinc fingers, a SET domain, a post-SET domain and a RING-type zinc finger. This protein is a member of the ASC-2/NCOA6 complex (ASCOM), which possesses histone methylation activity and is involved in transcriptional coactivation. [provided by RefSeq, Jul 2008]","start":152134922,"end":152436005,"strand":-1,"description":"lysine methyltransferase 2C [Source:HGNC Symbol;Acc:HGNC:13726]"}, {"versioned_ensembl_gene_id":"ENSG00000172380.5","gene_symbol":"GNG12","gene_name":"G protein subunit gamma 12 [Source:HGNC Symbol;Acc:HGNC:19663]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55970","summary":null,"start":67701466,"end":67833467,"strand":-1,"description":"G protein subunit gamma 12 [Source:HGNC Symbol;Acc:HGNC:19663]"}, {"versioned_ensembl_gene_id":"ENSG00000228987.9","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32414554,"end":32419764,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000164897.12","gene_symbol":"TMUB1","gene_name":"transmembrane and ubiquitin like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21709]","synonyms":"SB144,C7orf21","biotype":"protein_coding","ncbi_id":"83590","summary":null,"start":151081080,"end":151083546,"strand":-1,"description":"transmembrane and ubiquitin like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21709]"}, {"versioned_ensembl_gene_id":"ENSG00000225790.1","gene_symbol":"AC007953.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177934823,"end":177937662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188649.12","gene_symbol":"CC2D2B","gene_name":"coiled-coil and C2 domain containing 2B [Source:HGNC Symbol;Acc:HGNC:31666]","synonyms":"bA248J23.4,C10orf131,C10orf130,bA690P14.3","biotype":"protein_coding","ncbi_id":"387707","summary":null,"start":95907603,"end":96032684,"strand":1,"description":"coiled-coil and C2 domain containing 2B [Source:HGNC Symbol;Acc:HGNC:31666]"}, {"versioned_ensembl_gene_id":"ENSG00000186924.3","gene_symbol":"KRTAP22-1","gene_name":"keratin associated protein 22-1 [Source:HGNC Symbol;Acc:HGNC:18947]","synonyms":"KAP22.1","biotype":"protein_coding","ncbi_id":"337979","summary":null,"start":30601087,"end":30601382,"strand":1,"description":"keratin associated protein 22-1 [Source:HGNC Symbol;Acc:HGNC:18947]"}, {"versioned_ensembl_gene_id":"ENSG00000232040.2","gene_symbol":"ZBED9","gene_name":"zinc finger BED-type containing 9 [Source:HGNC Symbol;Acc:HGNC:13851]","synonyms":"ZNF452,ZNF305P2,ZFP38-L,SCAND3,KIAA1925,FLJ31087,Buster4","biotype":"protein_coding","ncbi_id":"114821","summary":null,"start":28571630,"end":28616212,"strand":-1,"description":"zinc finger BED-type containing 9 [Source:HGNC Symbol;Acc:HGNC:13851]"}, {"versioned_ensembl_gene_id":"ENSG00000233234.1","gene_symbol":"AL592464.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2811850,"end":2812692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186967.6","gene_symbol":"KRTAP19-4","gene_name":"keratin associated protein 19-4 [Source:HGNC Symbol;Acc:HGNC:18939]","synonyms":"KAP19.4","biotype":"protein_coding","ncbi_id":"337971","summary":null,"start":30496824,"end":30497133,"strand":-1,"description":"keratin associated protein 19-4 [Source:HGNC Symbol;Acc:HGNC:18939]"}, {"versioned_ensembl_gene_id":"ENSG00000151379.3","gene_symbol":"MSGN1","gene_name":"mesogenin 1 [Source:HGNC Symbol;Acc:HGNC:14907]","synonyms":"pMesogenin1","biotype":"protein_coding","ncbi_id":"343930","summary":null,"start":17816496,"end":17817101,"strand":1,"description":"mesogenin 1 [Source:HGNC Symbol;Acc:HGNC:14907]"}, {"versioned_ensembl_gene_id":"ENSG00000273595.1","gene_symbol":"AC092106.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106207394,"end":106208115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244502.2","gene_symbol":"HDAC11-AS1","gene_name":"HDAC11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40868]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874101","summary":null,"start":13476982,"end":13480053,"strand":-1,"description":"HDAC11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40868]"}, {"versioned_ensembl_gene_id":"ENSG00000236550.1","gene_symbol":"AL109809.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1676662,"end":1676907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236676.1","gene_symbol":"AC117944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81585941,"end":81625713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075240.16","gene_symbol":"GRAMD4","gene_name":"GRAM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29113]","synonyms":"KIAA0767,DIP","biotype":"protein_coding","ncbi_id":"23151","summary":"GRAMD4 is a mitochondrial effector of E2F1 (MIM 189971)-induced apoptosis (Stanelle et al., 2005 [PubMed 15565177]).[supplied by OMIM, Jan 2011]","start":46576012,"end":46679790,"strand":1,"description":"GRAM domain containing 4 [Source:HGNC Symbol;Acc:HGNC:29113]"}, {"versioned_ensembl_gene_id":"ENSG00000237716.1","gene_symbol":"AL136309.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4186624,"end":4188109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236769.1","gene_symbol":"AL139237.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43901365,"end":43912326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213147.3","gene_symbol":"RPL23AP60","gene_name":"ribosomal protein L23a pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:35966]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728933","summary":null,"start":133778246,"end":133778699,"strand":1,"description":"ribosomal protein L23a pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:35966]"}, {"versioned_ensembl_gene_id":"ENSG00000121350.15","gene_symbol":"PYROXD1","gene_name":"pyridine nucleotide-disulphide oxidoreductase domain 1 [Source:HGNC Symbol;Acc:HGNC:26162]","synonyms":"FLJ22028,DKFZp762G094","biotype":"protein_coding","ncbi_id":"79912","summary":"This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11. [provided by RefSeq, Apr 2017]","start":21437615,"end":21471252,"strand":1,"description":"pyridine nucleotide-disulphide oxidoreductase domain 1 [Source:HGNC Symbol;Acc:HGNC:26162]"}, {"versioned_ensembl_gene_id":"ENSG00000227770.1","gene_symbol":"RPL7P12","gene_name":"ribosomal protein L7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131085","summary":null,"start":38231568,"end":38232317,"strand":1,"description":"ribosomal protein L7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36611]"}, {"versioned_ensembl_gene_id":"ENSG00000237202.1","gene_symbol":"AJ239321.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13120244,"end":13120807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267635.1","gene_symbol":"AC209539.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41265358,"end":41265882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266984.1","gene_symbol":"POLR3GP2","gene_name":"RNA polymerase III subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50691]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422391","summary":null,"start":48478561,"end":48479228,"strand":1,"description":"RNA polymerase III subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50691]"}, {"versioned_ensembl_gene_id":"ENSG00000277907.1","gene_symbol":"AC024288.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48478282,"end":48478491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262121.2","gene_symbol":"KRTAP4-9","gene_name":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]","synonyms":"KAP4.9","biotype":"protein_coding","ncbi_id":"100132386","summary":null,"start":41105751,"end":41106907,"strand":1,"description":"keratin associated protein 4-9 [Source:HGNC Symbol;Acc:HGNC:18910]"}, {"versioned_ensembl_gene_id":"ENSG00000211673.2","gene_symbol":"IGLV3-1","gene_name":"immunoglobulin lambda variable 3-1 [Source:HGNC Symbol;Acc:HGNC:5896]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28809","summary":null,"start":22880706,"end":22881396,"strand":1,"description":"immunoglobulin lambda variable 3-1 [Source:HGNC Symbol;Acc:HGNC:5896]"}, {"versioned_ensembl_gene_id":"ENSG00000253963.1","gene_symbol":"IGLV3-2","gene_name":"immunoglobulin lambda variable 3-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5904]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28808","summary":null,"start":22873212,"end":22873440,"strand":1,"description":"immunoglobulin lambda variable 3-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5904]"}, {"versioned_ensembl_gene_id":"ENSG00000243094.1","gene_symbol":"AC079203.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34085911,"end":34086314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273388.1","gene_symbol":"AC005291.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10291820,"end":10317926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128881.16","gene_symbol":"TTBK2","gene_name":"tau tubulin kinase 2 [Source:HGNC Symbol;Acc:HGNC:19141]","synonyms":"SCA11,KIAA0847","biotype":"protein_coding","ncbi_id":"146057","summary":"This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem. [provided by RefSeq, Aug 2009]","start":42738734,"end":42920809,"strand":-1,"description":"tau tubulin kinase 2 [Source:HGNC Symbol;Acc:HGNC:19141]"}, {"versioned_ensembl_gene_id":"ENSG00000276998.1","gene_symbol":"REXO1L2P","gene_name":"REXO1 like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288527","summary":null,"start":85775106,"end":85779090,"strand":-1,"description":"REXO1 like 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32239]"}, {"versioned_ensembl_gene_id":"ENSG00000223665.1","gene_symbol":"AC000058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91638847,"end":91643512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237784.1","gene_symbol":"AC097713.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":234329483,"end":234329838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205176.3","gene_symbol":"REXO1L1P","gene_name":"REXO1 like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:24660]","synonyms":"REXO1L1,GOR","biotype":"transcribed_processed_pseudogene","ncbi_id":"254958","summary":null,"start":85656442,"end":85663497,"strand":-1,"description":"REXO1 like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:24660]"}, {"versioned_ensembl_gene_id":"ENSG00000082805.19","gene_symbol":"ERC1","gene_name":"ELKS/RAB6-interacting/CAST family member 1 [Source:HGNC Symbol;Acc:HGNC:17072]","synonyms":"ELKS,CAST2,RAB6IP2,MGC12974,KIAA1081","biotype":"protein_coding","ncbi_id":"23085","summary":"The protein encoded by this gene is a member of a family of RIM-binding proteins. RIMs are active zone proteins that regulate neurotransmitter release. This gene has been found fused to the receptor-type tyrosine kinase gene RET by gene rearrangement due to the translocation t(10;12)(q11;p13) in thyroid papillary carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":990509,"end":1495933,"strand":1,"description":"ELKS/RAB6-interacting/CAST family member 1 [Source:HGNC Symbol;Acc:HGNC:17072]"}, {"versioned_ensembl_gene_id":"ENSG00000182117.5","gene_symbol":"NOP10","gene_name":"NOP10 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14378]","synonyms":"NOP10P,NOLA3,MGC70651","biotype":"protein_coding","ncbi_id":"55505","summary":"This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA1 and NOLA2 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. The four H/ACA snoRNP proteins are also components of the telomerase complex. This gene encodes a protein related to Saccharomyces cerevisiae Nop10p. [provided by RefSeq, Jul 2008]","start":34341713,"end":34343177,"strand":-1,"description":"NOP10 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:14378]"}, {"versioned_ensembl_gene_id":"ENSG00000226935.6","gene_symbol":"LINC00161","gene_name":"long intergenic non-protein coding RNA 161 [Source:HGNC Symbol;Acc:HGNC:17138]","synonyms":"NCRNA00161,C21orf100","biotype":"lincRNA","ncbi_id":"118421","summary":null,"start":28539318,"end":28540355,"strand":1,"description":"long intergenic non-protein coding RNA 161 [Source:HGNC Symbol;Acc:HGNC:17138]"}, {"versioned_ensembl_gene_id":"ENSG00000254779.4","gene_symbol":"EGLN1P1","gene_name":"egl-9 family hypoxia inducible factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44481]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"106660614","summary":null,"start":84633874,"end":84634635,"strand":1,"description":"egl-9 family hypoxia inducible factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44481]"}, {"versioned_ensembl_gene_id":"ENSG00000157870.14","gene_symbol":"FAM213B","gene_name":"family with sequence similarity 213 member B [Source:HGNC Symbol;Acc:HGNC:28390]","synonyms":"MGC26818,C1orf93","biotype":"protein_coding","ncbi_id":"127281","summary":null,"start":2586491,"end":2591469,"strand":1,"description":"family with sequence similarity 213 member B [Source:HGNC Symbol;Acc:HGNC:28390]"}, {"versioned_ensembl_gene_id":"ENSG00000258240.5","gene_symbol":"AC002351.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110951683,"end":110957812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186153.16","gene_symbol":"WWOX","gene_name":"WW domain containing oxidoreductase [Source:HGNC Symbol;Acc:HGNC:12799]","synonyms":"WOX1,SDR41C1,FOR","biotype":"protein_coding","ncbi_id":"51741","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":78099413,"end":79212667,"strand":1,"description":"WW domain containing oxidoreductase [Source:HGNC Symbol;Acc:HGNC:12799]"}, {"versioned_ensembl_gene_id":"ENSG00000148655.14","gene_symbol":"LRMDA","gene_name":"leucine rich melanocyte differentiation associated [Source:HGNC Symbol;Acc:HGNC:23405]","synonyms":"OCA7,CDA017,C10orf11","biotype":"protein_coding","ncbi_id":"83938","summary":"This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]","start":75431453,"end":76560167,"strand":1,"description":"leucine rich melanocyte differentiation associated [Source:HGNC Symbol;Acc:HGNC:23405]"}, {"versioned_ensembl_gene_id":"ENSG00000262068.3","gene_symbol":"KRTAP3-1","gene_name":"keratin associated protein 3-1 [Source:HGNC Symbol;Acc:HGNC:16778]","synonyms":"KAP3.1","biotype":"protein_coding","ncbi_id":"83896","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41008648,"end":41019451,"strand":-1,"description":"keratin associated protein 3-1 [Source:HGNC Symbol;Acc:HGNC:16778]"}, {"versioned_ensembl_gene_id":"ENSG00000104327.7","gene_symbol":"CALB1","gene_name":"calbindin 1 [Source:HGNC Symbol;Acc:HGNC:1434]","synonyms":"CALB","biotype":"protein_coding","ncbi_id":"793","summary":"The protein encoded by this gene is a member of the calcium-binding protein superfamily that includes calmodulin and troponin C. Originally described as a 27 kDa protein, it is now known to be a 28 kDa protein. It contains four active calcium-binding domains, and has two modified domains that are thought to have lost their calcium binding capability. This protein is thought to buffer entry of calcium upon stimulation of glutamate receptors. Depletion of this protein was noted in patients with Huntington disease. [provided by RefSeq, Jan 2015]","start":90058608,"end":90095475,"strand":-1,"description":"calbindin 1 [Source:HGNC Symbol;Acc:HGNC:1434]"}, {"versioned_ensembl_gene_id":"ENSG00000231849.1","gene_symbol":"UBE2V2P4","gene_name":"ubiquitin conjugating enzyme E2 V2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44892]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480802","summary":null,"start":36241898,"end":36242156,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44892]"}, {"versioned_ensembl_gene_id":"ENSG00000188056.11","gene_symbol":"TREML4","gene_name":"triggering receptor expressed on myeloid cells like 4 [Source:HGNC Symbol;Acc:HGNC:30807]","synonyms":"TLT4","biotype":"protein_coding","ncbi_id":"285852","summary":null,"start":41228324,"end":41238882,"strand":1,"description":"triggering receptor expressed on myeloid cells like 4 [Source:HGNC Symbol;Acc:HGNC:30807]"}, {"versioned_ensembl_gene_id":"ENSG00000171219.8","gene_symbol":"CDC42BPG","gene_name":"CDC42 binding protein kinase gamma [Source:HGNC Symbol;Acc:HGNC:29829]","synonyms":"MRCKgamma,kappa-200,HSMDPKIN,DMPK2","biotype":"protein_coding","ncbi_id":"55561","summary":null,"start":64823387,"end":64844569,"strand":-1,"description":"CDC42 binding protein kinase gamma [Source:HGNC Symbol;Acc:HGNC:29829]"}, {"versioned_ensembl_gene_id":"ENSG00000187658.6","gene_symbol":"C5orf52","gene_name":"chromosome 5 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:35121]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100190949","summary":null,"start":157671553,"end":157680143,"strand":1,"description":"chromosome 5 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:35121]"}, {"versioned_ensembl_gene_id":"ENSG00000232960.10","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb1,Ckb2","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31704690,"end":31711736,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000236439.4","gene_symbol":"AC099336.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202471864,"end":202472117,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255455.2","gene_symbol":"AP003486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130866254,"end":130870247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132600.16","gene_symbol":"PRMT7","gene_name":"protein arginine methyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:25557]","synonyms":"FLJ10640,KIAA1933","biotype":"protein_coding","ncbi_id":"54496","summary":"This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017]","start":68310974,"end":68358563,"strand":1,"description":"protein arginine methyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:25557]"}, {"versioned_ensembl_gene_id":"ENSG00000151287.16","gene_symbol":"TEX30","gene_name":"testis expressed 30 [Source:HGNC Symbol;Acc:HGNC:25188]","synonyms":"C13orf27","biotype":"protein_coding","ncbi_id":"93081","summary":null,"start":102765990,"end":102773811,"strand":-1,"description":"testis expressed 30 [Source:HGNC Symbol;Acc:HGNC:25188]"}, {"versioned_ensembl_gene_id":"ENSG00000276408.1","gene_symbol":"AC025287.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75556392,"end":75557059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111554.14","gene_symbol":"MDM1","gene_name":"Mdm1 nuclear protein [Source:HGNC Symbol;Acc:HGNC:29917]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56890","summary":"This gene encodes a microtubule-binding nuclear protein that localizes to the centrioles of dividing cells and differentiating multiciliated cells and negatively regulates centriole duplication. The encoded protein is closely associated with the centriole barrel, and resides in the centriole lumen. Naturally-occurring mutations in the orthologous mouse gene are associated with age-related retinal degeneration. [provided by RefSeq, Feb 2019]","start":68272443,"end":68332381,"strand":-1,"description":"Mdm1 nuclear protein [Source:HGNC Symbol;Acc:HGNC:29917]"}, {"versioned_ensembl_gene_id":"ENSG00000261101.2","gene_symbol":"AC234775.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":101627868,"end":101628523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000034713.7","gene_symbol":"GABARAPL2","gene_name":"GABA type A receptor associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13291]","synonyms":"GEF2,GATE16,GATE-16,ATG8C,ATG8","biotype":"protein_coding","ncbi_id":"11345","summary":null,"start":75566351,"end":75577881,"strand":1,"description":"GABA type A receptor associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13291]"}, {"versioned_ensembl_gene_id":"ENSG00000275832.4","gene_symbol":"ARHGAP23","gene_name":"Rho GTPase activating protein 23 [Source:HGNC Symbol;Acc:HGNC:29293]","synonyms":"KIAA1501","biotype":"protein_coding","ncbi_id":"57636","summary":"The RHO (see ARHA; MIM 165390) family of small GTPases are involved in signal transduction through transmembrane receptors, and they are inactive in the GDP-bound form and active in the GTP-bound form. GTPase-activating proteins, such as ARHGAP23, inactivate RHO family proteins by stimulating their hydrolysis of GTP (Katoh and Katoh, 2004 [PubMed 15254754]).[supplied by OMIM, Mar 2008]","start":38419280,"end":38512392,"strand":1,"description":"Rho GTPase activating protein 23 [Source:HGNC Symbol;Acc:HGNC:29293]"}, {"versioned_ensembl_gene_id":"ENSG00000113749.7","gene_symbol":"HRH2","gene_name":"histamine receptor H2 [Source:HGNC Symbol;Acc:HGNC:5183]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3274","summary":"Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. Its various actions are mediated by histamine receptors H1, H2, H3 and H4. Histamine receptor H2 belongs to the family 1 of G protein-coupled receptors. It is an integral membrane protein and stimulates gastric acid secretion. It also regulates gastrointestinal motility and intestinal secretion and is thought to be involved in regulating cell growth and differentiation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":175658030,"end":175710756,"strand":1,"description":"histamine receptor H2 [Source:HGNC Symbol;Acc:HGNC:5183]"}, {"versioned_ensembl_gene_id":"ENSG00000254015.1","gene_symbol":"MTND4LP26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42260]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075104","summary":null,"start":18200924,"end":18201205,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42260]"}, {"versioned_ensembl_gene_id":"ENSG00000226594.1","gene_symbol":"AL356421.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47729827,"end":47740741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230615.6","gene_symbol":"AL139220.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44030443,"end":44115913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233464.2","gene_symbol":"AL589963.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152545930,"end":152546984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228581.9","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30619830,"end":30635627,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000244099.1","gene_symbol":"RPS23P3","gene_name":"ribosomal protein S23 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35499]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271091","summary":null,"start":66431092,"end":66431521,"strand":1,"description":"ribosomal protein S23 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35499]"}, {"versioned_ensembl_gene_id":"ENSG00000166558.10","gene_symbol":"SLC38A8","gene_name":"solute carrier family 38 member 8 [Source:HGNC Symbol;Acc:HGNC:32434]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146167","summary":"This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]","start":84009667,"end":84042636,"strand":-1,"description":"solute carrier family 38 member 8 [Source:HGNC Symbol;Acc:HGNC:32434]"}, {"versioned_ensembl_gene_id":"ENSG00000066230.10","gene_symbol":"SLC9A3","gene_name":"solute carrier family 9 member A3 [Source:HGNC Symbol;Acc:HGNC:11073]","synonyms":"NHE3","biotype":"protein_coding","ncbi_id":"6550","summary":"The protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22. [provided by RefSeq, Mar 2016]","start":473310,"end":524332,"strand":-1,"description":"solute carrier family 9 member A3 [Source:HGNC Symbol;Acc:HGNC:11073]"}, {"versioned_ensembl_gene_id":"ENSG00000265445.1","gene_symbol":"AC005703.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15261015,"end":15265707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276164.1","gene_symbol":"DUX4L20","gene_name":"double homeobox 4 like 20 [Source:HGNC Symbol;Acc:HGNC:50801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723538","summary":null,"start":133683668,"end":133684936,"strand":1,"description":"double homeobox 4 like 20 [Source:HGNC Symbol;Acc:HGNC:50801]"}, {"versioned_ensembl_gene_id":"ENSG00000178719.16","gene_symbol":"GRINA","gene_name":"glutamate ionotropic receptor NMDA type subunit associated protein 1 [Source:HGNC Symbol;Acc:HGNC:4589]","synonyms":"TMBIM3,NMDARA1,LFG1,HNRGW","biotype":"protein_coding","ncbi_id":"2907","summary":null,"start":143990058,"end":143993415,"strand":1,"description":"glutamate ionotropic receptor NMDA type subunit associated protein 1 [Source:HGNC Symbol;Acc:HGNC:4589]"}, {"versioned_ensembl_gene_id":"ENSG00000266994.1","gene_symbol":"AC020663.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":4730115,"end":4752565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237786.1","gene_symbol":"GFOD1-AS1","gene_name":"GFOD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40956]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874025","summary":null,"start":13486294,"end":13486852,"strand":1,"description":"GFOD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40956]"}, {"versioned_ensembl_gene_id":"ENSG00000243929.1","gene_symbol":"AC104784.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51978079,"end":51978372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255892.1","gene_symbol":"NDFIP1P1","gene_name":"Nedd4 family interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420792","summary":null,"start":18358443,"end":18358967,"strand":-1,"description":"Nedd4 family interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49866]"}, {"versioned_ensembl_gene_id":"ENSG00000145990.10","gene_symbol":"GFOD1","gene_name":"glucose-fructose oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21096]","synonyms":"FLJ20330,C6orf114,ADG-90","biotype":"protein_coding","ncbi_id":"54438","summary":null,"start":13357830,"end":13487662,"strand":-1,"description":"glucose-fructose oxidoreductase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21096]"}, {"versioned_ensembl_gene_id":"ENSG00000103199.13","gene_symbol":"ZNF500","gene_name":"zinc finger protein 500 [Source:HGNC Symbol;Acc:HGNC:23716]","synonyms":"ZSCAN50,ZKSCAN18,KIAA0557","biotype":"protein_coding","ncbi_id":"26048","summary":null,"start":4748239,"end":4767624,"strand":-1,"description":"zinc finger protein 500 [Source:HGNC Symbol;Acc:HGNC:23716]"}, {"versioned_ensembl_gene_id":"ENSG00000260669.2","gene_symbol":"AL096870.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":24209646,"end":24215987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119614.2","gene_symbol":"VSX2","gene_name":"visual system homeobox 2 [Source:HGNC Symbol;Acc:HGNC:1975]","synonyms":"RET1,HOX10,CHX10","biotype":"protein_coding","ncbi_id":"338917","summary":"This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009]","start":74239472,"end":74262738,"strand":1,"description":"visual system homeobox 2 [Source:HGNC Symbol;Acc:HGNC:1975]"}, {"versioned_ensembl_gene_id":"ENSG00000235064.1","gene_symbol":"SLC25A5P2","gene_name":"solute carrier family 25 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35470]","synonyms":"LOC344371","biotype":"processed_pseudogene","ncbi_id":"344371","summary":null,"start":33839782,"end":33840678,"strand":-1,"description":"solute carrier family 25 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35470]"}, {"versioned_ensembl_gene_id":"ENSG00000187999.4","gene_symbol":"HNRNPA1P61","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:48791]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288283","summary":null,"start":33636502,"end":33637425,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:48791]"}, {"versioned_ensembl_gene_id":"ENSG00000238038.1","gene_symbol":"ATP6V0E1P3","gene_name":"ATPase H+ transporting V0 subunit e1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133262","summary":null,"start":33602041,"end":33602286,"strand":1,"description":"ATPase H+ transporting V0 subunit e1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41937]"}, {"versioned_ensembl_gene_id":"ENSG00000233077.1","gene_symbol":"LINC01271","gene_name":"long intergenic non-protein coding RNA 1271 [Source:HGNC Symbol;Acc:HGNC:50327]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927586","summary":null,"start":50310711,"end":50321342,"strand":-1,"description":"long intergenic non-protein coding RNA 1271 [Source:HGNC Symbol;Acc:HGNC:50327]"}, {"versioned_ensembl_gene_id":"ENSG00000108784.9","gene_symbol":"NAGLU","gene_name":"N-acetyl-alpha-glucosaminidase [Source:HGNC Symbol;Acc:HGNC:7632]","synonyms":"NAG","biotype":"protein_coding","ncbi_id":"4669","summary":"This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate. [provided by RefSeq, Jul 2008]","start":42536172,"end":42544449,"strand":1,"description":"N-acetyl-alpha-glucosaminidase [Source:HGNC Symbol;Acc:HGNC:7632]"}, {"versioned_ensembl_gene_id":"ENSG00000225899.7","gene_symbol":"FRG2B","gene_name":"FSHD region gene 2 family member B [Source:HGNC Symbol;Acc:HGNC:33518]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441581","summary":null,"start":133623895,"end":133626795,"strand":-1,"description":"FSHD region gene 2 family member B [Source:HGNC Symbol;Acc:HGNC:33518]"}, {"versioned_ensembl_gene_id":"ENSG00000235086.1","gene_symbol":"FNDC1-IT1","gene_name":"FNDC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41460]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874312","summary":null,"start":159240786,"end":159243329,"strand":1,"description":"FNDC1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41460]"}, {"versioned_ensembl_gene_id":"ENSG00000233682.3","gene_symbol":"AL356417.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":159165899,"end":159170007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271148.1","gene_symbol":"AC023762.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49906863,"end":49907446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136492.8","gene_symbol":"BRIP1","gene_name":"BRCA1 interacting protein C-terminal helicase 1 [Source:HGNC Symbol;Acc:HGNC:20473]","synonyms":"OF,FANCJ,BACH1","biotype":"protein_coding","ncbi_id":"83990","summary":"The protein encoded by this gene is a member of the RecQ DEAH helicase family and interacts with the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double-strand break repair function of breast cancer, type 1 (BRCA1). This gene may be a target of germline cancer-inducing mutations. [provided by RefSeq, Jul 2008]","start":61681266,"end":61863521,"strand":-1,"description":"BRCA1 interacting protein C-terminal helicase 1 [Source:HGNC Symbol;Acc:HGNC:20473]"}, {"versioned_ensembl_gene_id":"ENSG00000227225.1","gene_symbol":"MTND1P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42063]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873337","summary":null,"start":19602259,"end":19603208,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42063]"}, {"versioned_ensembl_gene_id":"ENSG00000226702.1","gene_symbol":"MIR217HG","gene_name":"MIR217 host gene [Source:HGNC Symbol;Acc:HGNC:50537]","synonyms":"MIR216BHG,MIR216AHG","biotype":"lincRNA","ncbi_id":"104355290","summary":null,"start":55963191,"end":56047326,"strand":-1,"description":"MIR217 host gene [Source:HGNC Symbol;Acc:HGNC:50537]"}, {"versioned_ensembl_gene_id":"ENSG00000115415.18","gene_symbol":"STAT1","gene_name":"signal transducer and activator of transcription 1 [Source:HGNC Symbol;Acc:HGNC:11362]","synonyms":"STAT91,ISGF-3","biotype":"protein_coding","ncbi_id":"6772","summary":"The protein encoded by this gene is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. The protein encoded by this gene can be activated by various ligands including interferon-alpha, interferon-gamma, EGF, PDGF and IL6. This protein mediates the expression of a variety of genes, which is thought to be important for cell viability in response to different cell stimuli and pathogens. The protein plays an important role in immune responses to viral, fungal and mycobacterial pathogens. Mutations in this gene are associated with Immunodeficiency 31B, 31A, and 31C. [provided by RefSeq, Jun 2020]","start":190964358,"end":191020960,"strand":-1,"description":"signal transducer and activator of transcription 1 [Source:HGNC Symbol;Acc:HGNC:11362]"}, {"versioned_ensembl_gene_id":"ENSG00000149380.11","gene_symbol":"P4HA3","gene_name":"prolyl 4-hydroxylase subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:30135]","synonyms":"C-P4Halpha(III)","biotype":"protein_coding","ncbi_id":"283208","summary":"This gene encodes a component of prolyl 4-hydroxylase, a key enzyme in collagen synthesis composed of two identical alpha subunits and two beta subunits. The encoded protein is one of several different types of alpha subunits and provides the major part of the catalytic site of the active enzyme. In collagen and related proteins, prolyl 4-hydroxylase catalyzes the formation of 4-hydroxyproline that is essential to the proper three-dimensional folding of newly synthesized procollagen chains. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":74235801,"end":74311657,"strand":-1,"description":"prolyl 4-hydroxylase subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:30135]"}, {"versioned_ensembl_gene_id":"ENSG00000263125.1","gene_symbol":"AC005951.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54754165,"end":54754649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263189.1","gene_symbol":"AC023934.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53952936,"end":53955324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242612.6","gene_symbol":"DECR2","gene_name":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]","synonyms":"SDR17C1,PDCR","biotype":"protein_coding","ncbi_id":"26063","summary":null,"start":401826,"end":412487,"strand":1,"description":"2,4-dienoyl-CoA reductase 2 [Source:HGNC Symbol;Acc:HGNC:2754]"}, {"versioned_ensembl_gene_id":"ENSG00000274442.2","gene_symbol":"PRPF8","gene_name":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]","synonyms":"RP13,PRPC8,Prp8,hPrp8,SNRNP220","biotype":"protein_coding","ncbi_id":"10594","summary":"Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2- and U12-dependent spliceosomes, and found to be essential for the catalytic step II in pre-mRNA splicing process. It contains several WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":1650629,"end":1684882,"strand":-1,"description":"pre-mRNA processing factor 8 [Source:HGNC Symbol;Acc:HGNC:17340]"}, {"versioned_ensembl_gene_id":"ENSG00000225755.2","gene_symbol":"AL451063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":163237214,"end":163239197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236004.2","gene_symbol":"AL139156.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52189916,"end":52190309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224108.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30026870,"end":30028160,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000258947.6","gene_symbol":"TUBB3","gene_name":"tubulin beta 3 class III [Source:HGNC Symbol;Acc:HGNC:20772]","synonyms":"FEOM3,CFEOM3A,CFEOM3,beta-4","biotype":"protein_coding","ncbi_id":"10381","summary":"This gene encodes a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Oct 2010]","start":89921392,"end":89938761,"strand":1,"description":"tubulin beta 3 class III [Source:HGNC Symbol;Acc:HGNC:20772]"}, {"versioned_ensembl_gene_id":"ENSG00000282325.1","gene_symbol":"AC244207.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45452499,"end":45463720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105197.10","gene_symbol":"TIMM50","gene_name":"translocase of inner mitochondrial membrane 50 [Source:HGNC Symbol;Acc:HGNC:23656]","synonyms":"TIM50L","biotype":"protein_coding","ncbi_id":"92609","summary":"This gene encodes a subunit of the TIM23 inner mitochondrial membrane translocase complex. The encoded protein functions as the receptor subunit that recognizes the mitochondrial targeting signal, or presequence, on protein cargo that is destined for the mitochondrial inner membrane and matrix. This protein may also play a role in maintaining the membrane permeability barrier, and knockdown of this gene in human cells results in the release of cytochrome c and apoptosis. [provided by RefSeq, Jul 2016]","start":39480412,"end":39493785,"strand":1,"description":"translocase of inner mitochondrial membrane 50 [Source:HGNC Symbol;Acc:HGNC:23656]"}, {"versioned_ensembl_gene_id":"ENSG00000125520.13","gene_symbol":"SLC2A4RG","gene_name":"SLC2A4 regulator [Source:HGNC Symbol;Acc:HGNC:15930]","synonyms":"Si-1-2-19,Si-1-2,HDBP1,GEF","biotype":"protein_coding","ncbi_id":"56731","summary":"The protein encoded by this gene is a nuclear transcription factor involved in the activation of the solute carrier family 2 member 4 gene. The encoded protein interacts with another transcription factor, myocyte enhancer factor 2, to activate transcription of this gene. [provided by RefSeq, Jul 2008]","start":63739861,"end":63743505,"strand":1,"description":"SLC2A4 regulator [Source:HGNC Symbol;Acc:HGNC:15930]"}, {"versioned_ensembl_gene_id":"ENSG00000234638.1","gene_symbol":"AC053503.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219425071,"end":219426184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104375.15","gene_symbol":"STK3","gene_name":"serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:11406]","synonyms":"MST2,KRS1","biotype":"protein_coding","ncbi_id":"6788","summary":"This gene encodes a serine/threonine protein kinase activated by proapoptotic molecules indicating the encoded protein functions as a growth suppressor. Cleavage of the protein product by caspase removes the inhibitory C-terminal portion. The N-terminal portion is transported to the nucleus where it homodimerizes to form the active kinase which promotes the condensation of chromatin during apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":98401403,"end":98942827,"strand":-1,"description":"serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:11406]"}, {"versioned_ensembl_gene_id":"ENSG00000112062.10","gene_symbol":"MAPK14","gene_name":"mitogen-activated protein kinase 14 [Source:HGNC Symbol;Acc:HGNC:6876]","synonyms":"PRKM15,PRKM14,p38,Mxi2,CSPB1,CSBP2,CSBP1","biotype":"protein_coding","ncbi_id":"1432","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various environmental stresses and proinflammatory cytokines. The activation requires its phosphorylation by MAP kinase kinases (MKKs), or its autophosphorylation triggered by the interaction of MAP3K7IP1/TAB1 protein with this kinase. The substrates of this kinase include transcription regulator ATF2, MEF2C, and MAX, cell cycle regulator CDC25B, and tumor suppressor p53, which suggest the roles of this kinase in stress related transcription and cell cycle regulation, as well as in genotoxic stress response. Four alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":36027677,"end":36111236,"strand":1,"description":"mitogen-activated protein kinase 14 [Source:HGNC Symbol;Acc:HGNC:6876]"}, {"versioned_ensembl_gene_id":"ENSG00000225893.1","gene_symbol":"AL136231.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4633027,"end":4633756,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227355.2","gene_symbol":"AL359644.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":121369906,"end":121463237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157613.10","gene_symbol":"CREB3L1","gene_name":"cAMP responsive element binding protein 3 like 1 [Source:HGNC Symbol;Acc:HGNC:18856]","synonyms":"OASIS","biotype":"protein_coding","ncbi_id":"90993","summary":"The protein encoded by this gene is normally found in the membrane of the endoplasmic reticulum (ER). However, upon stress to the ER, the encoded protein is cleaved and the released cytoplasmic transcription factor domain translocates to the nucleus. There it activates the transcription of target genes by binding to box-B elements. [provided by RefSeq, Jun 2013]","start":46277661,"end":46321422,"strand":1,"description":"cAMP responsive element binding protein 3 like 1 [Source:HGNC Symbol;Acc:HGNC:18856]"}, {"versioned_ensembl_gene_id":"ENSG00000197057.9","gene_symbol":"DTHD1","gene_name":"death domain containing 1 [Source:HGNC Symbol;Acc:HGNC:37261]","synonyms":"FLJ16686","biotype":"protein_coding","ncbi_id":"401124","summary":"This gene encodes a protein which contains a death domain. Death domain-containing proteins function in signaling pathways and formation of signaling complexes, as well as the apoptosis pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":36281622,"end":36345756,"strand":1,"description":"death domain containing 1 [Source:HGNC Symbol;Acc:HGNC:37261]"}, {"versioned_ensembl_gene_id":"ENSG00000225000.1","gene_symbol":"AC010082.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18429062,"end":18430738,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257124.2","gene_symbol":"AC093025.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83661009,"end":83661719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196800.6","gene_symbol":"SPINK14","gene_name":"serine peptidase inhibitor, Kazal type 14 (putative) [Source:HGNC Symbol;Acc:HGNC:33825]","synonyms":"SPINK5L2","biotype":"protein_coding","ncbi_id":"408187","summary":null,"start":148169733,"end":148175398,"strand":1,"description":"serine peptidase inhibitor, Kazal type 14 (putative) [Source:HGNC Symbol;Acc:HGNC:33825]"}, {"versioned_ensembl_gene_id":"ENSG00000239219.2","gene_symbol":"AC008040.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169939353,"end":169966734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262461.5","gene_symbol":"SPDYE9P","gene_name":"speedy/RINGO cell cycle regulator family member E9, pseudogene [Source:HGNC Symbol;Acc:HGNC:45034]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643909","summary":null,"start":73076165,"end":73086038,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E9, pseudogene [Source:HGNC Symbol;Acc:HGNC:45034]"}, {"versioned_ensembl_gene_id":"ENSG00000223552.1","gene_symbol":"AC098613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46364955,"end":46407059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160791.13","gene_symbol":"CCR5","gene_name":"C-C motif chemokine receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:1606]","synonyms":"IDDM22,CMKBR5,CKR5,CKR-5,CD195,CC-CKR-5","biotype":"protein_coding","ncbi_id":"1234","summary":"This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. This protein is expressed by T cells and macrophages, and is known to be an important co-receptor for macrophage-tropic virus, including HIV, to enter host cells. Defective alleles of this gene have been associated with the HIV infection resistance. The ligands of this receptor include monocyte chemoattractant protein 2 (MCP-2), macrophage inflammatory protein 1 alpha (MIP-1 alpha), macrophage inflammatory protein 1 beta (MIP-1 beta) and regulated on activation normal T expressed and secreted protein (RANTES). Expression of this gene was also detected in a promyeloblastic cell line, suggesting that this protein may play a role in granulocyte lineage proliferation and differentiation. This gene is located at the chemokine receptor gene cluster region. An allelic polymorphism in this gene results in both functional and non-functional alleles; the reference genome represents the functional allele. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2015]","start":46370854,"end":46376206,"strand":1,"description":"C-C motif chemokine receptor 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:1606]"}, {"versioned_ensembl_gene_id":"ENSG00000121807.5","gene_symbol":"CCR2","gene_name":"C-C motif chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:1603]","synonyms":"MCP-1-R,FLJ78302,CMKBR2,CKR2,CD192,CC-CKR-2","biotype":"protein_coding","ncbi_id":"729230","summary":"The protein encoded by this gene is a receptor for monocyte chemoattractant protein-1, a chemokine which specifically mediates monocyte chemotaxis. Monocyte chemoattractant protein-1 is involved in monocyte infiltration in inflammatory diseases such as rheumatoid arthritis as well as in the inflammatory response against tumors. The encoded protein mediates agonist-dependent calcium mobilization and inhibition of adenylyl cyclase. This protein can also be a coreceptor with CD4 for HIV-1 infection. This gene is located in the chemokine receptor gene cluster region of chromosome 3. [provided by RefSeq, Aug 2017]","start":46353734,"end":46360928,"strand":1,"description":"C-C motif chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:1603]"}, {"versioned_ensembl_gene_id":"ENSG00000008952.16","gene_symbol":"SEC62","gene_name":"SEC62 homolog, preprotein translocation factor [Source:HGNC Symbol;Acc:HGNC:11846]","synonyms":"Dtrp1,TLOC1,HTP1","biotype":"protein_coding","ncbi_id":"7095","summary":"The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. The protein encoded by this gene and SEC63 protein are found to be associated with ribosome-free SEC61 complex. It is speculated that Sec61-Sec62-Sec63 may perform post-translational protein translocation into the ER. The Sec61-Sec62-Sec63 complex might also perform the backward transport of ER proteins that are subject to the ubiquitin-proteasome-dependent degradation pathway. The encoded protein is an integral membrane protein located in the rough ER. [provided by RefSeq, Jul 2008]","start":169966635,"end":169998373,"strand":1,"description":"SEC62 homolog, preprotein translocation factor [Source:HGNC Symbol;Acc:HGNC:11846]"}, {"versioned_ensembl_gene_id":"ENSG00000243775.2","gene_symbol":"OSTCP1","gene_name":"oligosaccharyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30530]","synonyms":"OSTCL,DC2L","biotype":"transcribed_processed_pseudogene","ncbi_id":"202459","summary":null,"start":158841117,"end":158857632,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30530]"}, {"versioned_ensembl_gene_id":"ENSG00000231288.1","gene_symbol":"CR759795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33112911,"end":33113320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183773.15","gene_symbol":"AIFM3","gene_name":"apoptosis inducing factor, mitochondria associated 3 [Source:HGNC Symbol;Acc:HGNC:26398]","synonyms":"FLJ30473,AIFL","biotype":"protein_coding","ncbi_id":"150209","summary":null,"start":20965108,"end":20981360,"strand":1,"description":"apoptosis inducing factor, mitochondria associated 3 [Source:HGNC Symbol;Acc:HGNC:26398]"}, {"versioned_ensembl_gene_id":"ENSG00000214285.2","gene_symbol":"NPS","gene_name":"neuropeptide S [Source:HGNC Symbol;Acc:HGNC:33940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"594857","summary":null,"start":127549369,"end":127552639,"strand":1,"description":"neuropeptide S [Source:HGNC Symbol;Acc:HGNC:33940]"}, {"versioned_ensembl_gene_id":"ENSG00000279725.1","gene_symbol":"AL391005.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127734562,"end":127736996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166900.16","gene_symbol":"STX3","gene_name":"syntaxin 3 [Source:HGNC Symbol;Acc:HGNC:11438]","synonyms":"STX3A","biotype":"protein_coding","ncbi_id":"6809","summary":"The gene is a member of the syntaxin family. The encoded protein is targeted to the apical membrane of epithelial cells where it forms clusters and is important in establishing and maintaining polarity necessary for protein trafficking involving vesicle fusion and exocytosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":59713456,"end":59805882,"strand":1,"description":"syntaxin 3 [Source:HGNC Symbol;Acc:HGNC:11438]"}, {"versioned_ensembl_gene_id":"ENSG00000172289.3","gene_symbol":"OR10V1","gene_name":"olfactory receptor family 10 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15136]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390201","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":59712916,"end":59713845,"strand":-1,"description":"olfactory receptor family 10 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15136]"}, {"versioned_ensembl_gene_id":"ENSG00000249180.1","gene_symbol":"AC020900.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96741079,"end":96742698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033627.16","gene_symbol":"ATP6V0A1","gene_name":"ATPase H+ transporting V0 subunit a1 [Source:HGNC Symbol;Acc:HGNC:865]","synonyms":"VPP1,Vph1,Stv1,ATP6N1A,ATP6N1,a1","biotype":"protein_coding","ncbi_id":"535","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes one of three A subunit proteins and the encoded protein is associated with clathrin-coated vesicles. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":42458844,"end":42522611,"strand":1,"description":"ATPase H+ transporting V0 subunit a1 [Source:HGNC Symbol;Acc:HGNC:865]"}, {"versioned_ensembl_gene_id":"ENSG00000239684.2","gene_symbol":"PTGER4P3","gene_name":"prostaglandin E receptor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874378","summary":null,"start":63775892,"end":63776143,"strand":-1,"description":"prostaglandin E receptor 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38498]"}, {"versioned_ensembl_gene_id":"ENSG00000261783.1","gene_symbol":"AC009054.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75379818,"end":75381260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262769.1","gene_symbol":"AC025627.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19560111,"end":19597922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183625.14","gene_symbol":"CCR3","gene_name":"C-C motif chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:1604]","synonyms":"CMKBR3,CKR3,CD193,CC-CKR-3","biotype":"protein_coding","ncbi_id":"1232","summary":"The protein encoded by this gene is a receptor for C-C type chemokines. It belongs to family 1 of the G protein-coupled receptors. This receptor binds and responds to a variety of chemokines, including eotaxin (CCL11), eotaxin-3 (CCL26), MCP-3 (CCL7), MCP-4 (CCL13), and RANTES (CCL5). It is highly expressed in eosinophils and basophils, and is also detected in TH1 and TH2 cells, as well as in airway epithelial cells. This receptor may contribute to the accumulation and activation of eosinophils and other inflammatory cells in the allergic airway. It is also known to be an entry co-receptor for HIV-1. This gene and seven other chemokine receptor genes form a chemokine receptor gene cluster on the chromosomal region 3p21. Alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2009]","start":46163604,"end":46266706,"strand":1,"description":"C-C motif chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:1604]"}, {"versioned_ensembl_gene_id":"ENSG00000092820.17","gene_symbol":"EZR","gene_name":"ezrin [Source:HGNC Symbol;Acc:HGNC:12691]","synonyms":"VIL2","biotype":"protein_coding","ncbi_id":"7430","summary":"The cytoplasmic peripheral membrane protein encoded by this gene functions as a protein-tyrosine kinase substrate in microvilli. As a member of the ERM protein family, this protein serves as an intermediate between the plasma membrane and the actin cytoskeleton. This protein plays a key role in cell surface structure adhesion, migration and organization, and it has been implicated in various human cancers. A pseudogene located on chromosome 3 has been identified for this gene. Alternatively spliced variants have also been described for this gene. [provided by RefSeq, Jul 2008]","start":158765741,"end":158819412,"strand":-1,"description":"ezrin [Source:HGNC Symbol;Acc:HGNC:12691]"}, {"versioned_ensembl_gene_id":"ENSG00000235027.1","gene_symbol":"AC068580.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1760348,"end":1762486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169035.11","gene_symbol":"KLK7","gene_name":"kallikrein related peptidase 7 [Source:HGNC Symbol;Acc:HGNC:6368]","synonyms":"SCCE,PRSS6","biotype":"protein_coding","ncbi_id":"5650","summary":"This gene encodes a member of the kallikrein subfamily of serine proteases. These enzymes have diverse physiological functions and many kallikrein genes are biomarkers for cancer. The encoded protein has chymotrypsin-like activity and plays a role in the proteolysis of intercellular cohesive structures that precedes desquamation, the shedding of the outermost layer of the epidermis. The encoded protein may play a role in cancer invasion and metastasis, and increased expression of this gene is associated with unfavorable prognosis and progression of several types of cancer. Polymorphisms in this gene may play a role in the development of atopic dermatitis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, which is one of fifteen kallikrein subfamily members located in a gene cluster on chromosome 19. [provided by RefSeq, May 2011]","start":50976482,"end":50984099,"strand":-1,"description":"kallikrein related peptidase 7 [Source:HGNC Symbol;Acc:HGNC:6368]"}, {"versioned_ensembl_gene_id":"ENSG00000231834.10","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29930208,"end":29934849,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000277016.2","gene_symbol":"IGHG4","gene_name":"immunoglobulin heavy constant gamma 4 (G4m marker) [Source:HGNC Symbol;Acc:HGNC:5528]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"3503","summary":null,"start":105625112,"end":105626837,"strand":-1,"description":"immunoglobulin heavy constant gamma 4 (G4m marker) [Source:HGNC Symbol;Acc:HGNC:5528]"}, {"versioned_ensembl_gene_id":"ENSG00000068097.14","gene_symbol":"HEATR6","gene_name":"HEAT repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:24076]","synonyms":"FLJ22087,ABC1","biotype":"protein_coding","ncbi_id":"63897","summary":null,"start":60043194,"end":60078931,"strand":-1,"description":"HEAT repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:24076]"}, {"versioned_ensembl_gene_id":"ENSG00000215695.1","gene_symbol":"RSC1A1","gene_name":"regulator of solute carriers 1 [Source:HGNC Symbol;Acc:HGNC:10458]","synonyms":"RS1","biotype":"protein_coding","ncbi_id":"6248","summary":"The protein encoded by this intronless gene inhibits the expression of the solute carrier family 5 (sodium/glucose cotransporter), member 1 gene (SLC5A1) and downregulates exocytosis of the SLC5A1 protein. The encoded protein is sometimes found coating the trans-Golgi network and other times is localized to the nucleus, depending on the cell cycle stage. This protein also inhibits the expression of solute carrier family 22 (organic cation transporter), member 2 (SLC22A2). [provided by RefSeq, Dec 2015]","start":15659869,"end":15661722,"strand":1,"description":"regulator of solute carriers 1 [Source:HGNC Symbol;Acc:HGNC:10458]"}, {"versioned_ensembl_gene_id":"ENSG00000184619.3","gene_symbol":"KRBA2","gene_name":"KRAB-A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26989]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124751","summary":null,"start":8368637,"end":8376711,"strand":-1,"description":"KRAB-A domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26989]"}, {"versioned_ensembl_gene_id":"ENSG00000143498.17","gene_symbol":"TAF1A","gene_name":"TATA-box binding protein associated factor, RNA polymerase I subunit A [Source:HGNC Symbol;Acc:HGNC:11532]","synonyms":"TAFI48,SL1","biotype":"protein_coding","ncbi_id":"9015","summary":"This gene encodes a subunit of the RNA polymerase I complex, Selectivity Factor I (SLI). The encoded protein is a TATA box-binding protein-associated factor that plays a role in the assembly of the RNA polymerase I preinitiation complex. Alternate splicing results in multiple transcript variants encoding multiple isoforms.[provided by RefSeq, Jan 2011]","start":222557902,"end":222589933,"strand":-1,"description":"TATA-box binding protein associated factor, RNA polymerase I subunit A [Source:HGNC Symbol;Acc:HGNC:11532]"}, {"versioned_ensembl_gene_id":"ENSG00000180409.3","gene_symbol":"OR10AA1P","gene_name":"olfactory receptor family 10 subfamily AA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14989]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81487","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158808399,"end":158809335,"strand":-1,"description":"olfactory receptor family 10 subfamily AA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14989]"}, {"versioned_ensembl_gene_id":"ENSG00000257530.1","gene_symbol":"AC048344.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32104117,"end":32107528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074266.19","gene_symbol":"EED","gene_name":"embryonic ectoderm development [Source:HGNC Symbol;Acc:HGNC:3188]","synonyms":"WAIT-1,HEED","biotype":"protein_coding","ncbi_id":"8726","summary":"This gene encodes a member of the Polycomb-group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein interacts with enhancer of zeste 2, the cytoplasmic tail of integrin beta7, immunodeficiency virus type 1 (HIV-1) MA protein, and histone deacetylase proteins. This protein mediates repression of gene activity through histone deacetylation, and may act as a specific regulator of integrin function. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":86244544,"end":86278813,"strand":1,"description":"embryonic ectoderm development [Source:HGNC Symbol;Acc:HGNC:3188]"}, {"versioned_ensembl_gene_id":"ENSG00000169918.9","gene_symbol":"OTUD7A","gene_name":"OTU deubiquitinase 7A [Source:HGNC Symbol;Acc:HGNC:20718]","synonyms":"OTUD7,CEZANNE2,C15orf16","biotype":"protein_coding","ncbi_id":"161725","summary":"The protein encoded by this gene is a deubiquitinizing enzyme and possible tumor suppressor. The encoded protein acts on TNF receptor associated factor 6 (TRAF6) to control nuclear factor kappa B expression. However, this gene is downregulated by SNAIL1 in hepatocellular carcinoma cells, contributing to their progression and malignancy. [provided by RefSeq, Aug 2016]","start":31475398,"end":31870789,"strand":-1,"description":"OTU deubiquitinase 7A [Source:HGNC Symbol;Acc:HGNC:20718]"}, {"versioned_ensembl_gene_id":"ENSG00000226352.2","gene_symbol":"PSPC1-AS2","gene_name":"PSPC1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:52951]","synonyms":"RP11-523H24.3","biotype":"antisense_RNA","ncbi_id":"109729130","summary":null,"start":19674624,"end":19675884,"strand":1,"description":"PSPC1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:52951]"}, {"versioned_ensembl_gene_id":"ENSG00000241728.5","gene_symbol":"AP001062.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":44328944,"end":44330221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259696.2","gene_symbol":"AC104759.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31453201,"end":31454139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248758.1","gene_symbol":"AC008883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97188090,"end":97201880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235655.3","gene_symbol":"H3F3AP4","gene_name":"H3 histone, family 3A, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42980]","synonyms":"p13","biotype":"processed_pseudogene","ncbi_id":"440926","summary":null,"start":174719908,"end":174720318,"strand":1,"description":"H3 histone, family 3A, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42980]"}, {"versioned_ensembl_gene_id":"ENSG00000219249.2","gene_symbol":"AMZ2P2","gene_name":"archaelysin family metallopeptidase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38072]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421018","summary":null,"start":158725747,"end":158726803,"strand":-1,"description":"archaelysin family metallopeptidase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38072]"}, {"versioned_ensembl_gene_id":"ENSG00000256008.2","gene_symbol":"AC125616.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120629611,"end":120641591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249768.2","gene_symbol":"HSPE1P10","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288235","summary":null,"start":126737438,"end":126737995,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49329]"}, {"versioned_ensembl_gene_id":"ENSG00000249451.1","gene_symbol":"AC021491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50503412,"end":50508328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196900.4","gene_symbol":"TEX43","gene_name":"testis expressed 43 [Source:HGNC Symbol;Acc:HGNC:33767]","synonyms":"Tseg7,MGC163369,MGC163367,FLJ27505,C5orf48","biotype":"protein_coding","ncbi_id":"389320","summary":null,"start":126631722,"end":126636287,"strand":1,"description":"testis expressed 43 [Source:HGNC Symbol;Acc:HGNC:33767]"}, {"versioned_ensembl_gene_id":"ENSG00000230929.5","gene_symbol":"AC099513.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126628019,"end":126628319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276727.1","gene_symbol":"AC137834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57229498,"end":57230198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235350.1","gene_symbol":"AL606490.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48433201,"end":48441619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130402.11","gene_symbol":"ACTN4","gene_name":"actinin alpha 4 [Source:HGNC Symbol;Acc:HGNC:166]","synonyms":"FSGS1","biotype":"protein_coding","ncbi_id":"81","summary":" Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a nonmuscle, alpha actinin isoform which is concentrated in the cytoplasm, and thought to be involved in metastatic processes. Mutations in this gene have been associated with focal and segmental glomerulosclerosis. [provided by RefSeq, Jul 2008]","start":38647649,"end":38731583,"strand":1,"description":"actinin alpha 4 [Source:HGNC Symbol;Acc:HGNC:166]"}, {"versioned_ensembl_gene_id":"ENSG00000231603.1","gene_symbol":"AL606490.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48412303,"end":48415285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235979.8","gene_symbol":"AC004448.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19417804,"end":19492991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182021.10","gene_symbol":"AL591379.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63111255,"end":63127100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126870.15","gene_symbol":"WDR60","gene_name":"WD repeat domain 60 [Source:HGNC Symbol;Acc:HGNC:21862]","synonyms":"FLJ10300,FAP163","biotype":"protein_coding","ncbi_id":"55112","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) and may facilitate the formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. The encoded protein contains four WD repeats and may play a role in the formation of cilia. Mutations in this gene have been associated with short-rib polydactyly and Jeune syndromes. [provided by RefSeq, Mar 2014]","start":158856578,"end":158956747,"strand":1,"description":"WD repeat domain 60 [Source:HGNC Symbol;Acc:HGNC:21862]"}, {"versioned_ensembl_gene_id":"ENSG00000172171.10","gene_symbol":"TEFM","gene_name":"transcription elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26223]","synonyms":"FLJ22729,C17orf42","biotype":"protein_coding","ncbi_id":"79736","summary":null,"start":30897336,"end":30906820,"strand":-1,"description":"transcription elongation factor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26223]"}, {"versioned_ensembl_gene_id":"ENSG00000119321.8","gene_symbol":"FKBP15","gene_name":"FK506 binding protein 15 [Source:HGNC Symbol;Acc:HGNC:23397]","synonyms":"PPP1R76,KIAA0674,FKBP133,WAFL","biotype":"protein_coding","ncbi_id":"23307","summary":null,"start":113161006,"end":113221361,"strand":-1,"description":"FK506 binding protein 15 [Source:HGNC Symbol;Acc:HGNC:23397]"}, {"versioned_ensembl_gene_id":"ENSG00000235487.8","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"C6orf16,SEEK1","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31107244,"end":31132550,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000249684.5","gene_symbol":"AC106795.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177950335,"end":177963960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234445.1","gene_symbol":"FGF14-AS1","gene_name":"FGF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40237]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874081","summary":null,"start":102367539,"end":102373666,"strand":1,"description":"FGF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40237]"}, {"versioned_ensembl_gene_id":"ENSG00000229975.1","gene_symbol":"LIPT1P1","gene_name":"lipoyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39278]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131188","summary":null,"start":102002125,"end":102003310,"strand":1,"description":"lipoyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39278]"}, {"versioned_ensembl_gene_id":"ENSG00000188282.12","gene_symbol":"RUFY4","gene_name":"RUN and FYVE domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24804]","synonyms":"ZFYVE31,FLJ46536","biotype":"protein_coding","ncbi_id":"285180","summary":null,"start":218034960,"end":218090581,"strand":1,"description":"RUN and FYVE domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24804]"}, {"versioned_ensembl_gene_id":"ENSG00000229754.1","gene_symbol":"CXCR2P1","gene_name":"C-X-C motif chemokine receptor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6028]","synonyms":"IL8RBP,CXCR2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3580","summary":null,"start":218059155,"end":218065729,"strand":-1,"description":"C-X-C motif chemokine receptor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6028]"}, {"versioned_ensembl_gene_id":"ENSG00000055163.19","gene_symbol":"CYFIP2","gene_name":"cytoplasmic FMR1 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:13760]","synonyms":"PIR121","biotype":"protein_coding","ncbi_id":"26999","summary":null,"start":157266079,"end":157395595,"strand":1,"description":"cytoplasmic FMR1 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:13760]"}, {"versioned_ensembl_gene_id":"ENSG00000255847.5","gene_symbol":"AP003717.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73963657,"end":73970287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112146.16","gene_symbol":"FBXO9","gene_name":"F-box protein 9 [Source:HGNC Symbol;Acc:HGNC:13588]","synonyms":"NY-REN-57,FBX9","biotype":"protein_coding","ncbi_id":"26268","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Alternative splicing of this gene generates at least 3 transcript variants diverging at the 5' terminus. [provided by RefSeq, Jul 2008]","start":53051991,"end":53100873,"strand":1,"description":"F-box protein 9 [Source:HGNC Symbol;Acc:HGNC:13588]"}, {"versioned_ensembl_gene_id":"ENSG00000280432.1","gene_symbol":"AP000962.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16525919,"end":16527019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273702.1","gene_symbol":"AC091271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59618553,"end":59619714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259112.2","gene_symbol":"NDUFC2-KCTD14","gene_name":"NDUFC2-KCTD14 readthrough [Source:HGNC Symbol;Acc:HGNC:42956]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532726","summary":"This locus represents naturally occurring read-through transcription between the neighboring NDUFC2 (NADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 2, 14.5kDa) and KCTD14 (potassium channel tetramerisation domain containing 14) genes on chromosome 11. The read-through transcripts share sequence identity with the upstream gene product and one variant has a frameshifted C-terminal region derived from the downstream gene exons. [provided by RefSeq, Feb 2011]","start":78016971,"end":78079865,"strand":-1,"description":"NDUFC2-KCTD14 readthrough [Source:HGNC Symbol;Acc:HGNC:42956]"}, {"versioned_ensembl_gene_id":"ENSG00000230102.7","gene_symbol":"LINC02028","gene_name":"long intergenic non-protein coding RNA 2028 [Source:HGNC Symbol;Acc:HGNC:27718]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285389","summary":null,"start":194005259,"end":194070970,"strand":-1,"description":"long intergenic non-protein coding RNA 2028 [Source:HGNC Symbol;Acc:HGNC:27718]"}, {"versioned_ensembl_gene_id":"ENSG00000221946.7","gene_symbol":"FXYD7","gene_name":"FXYD domain containing ion transport regulator 7 [Source:HGNC Symbol;Acc:HGNC:4034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53822","summary":"This reference sequence was derived from multiple replicate ESTs and validated by similar human genomic sequence. This gene encodes a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. The approved human gene nomenclature for the family is FXYD-domain containing ion transport regulator. Transmembrane topology has been established for two family members (FXYD1 and FXYD2), with the N-terminus extracellular and the C-terminus on the cytoplasmic side of the membrane. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. This gene product, FXYD7, is novel and has not been characterized as a protein. [RefSeq curation by Kathleen J. Sweadner, Ph.D., sweadner@helix.mgh.harvard.edu., Dec 2000]","start":35143250,"end":35154301,"strand":1,"description":"FXYD domain containing ion transport regulator 7 [Source:HGNC Symbol;Acc:HGNC:4034]"}, {"versioned_ensembl_gene_id":"ENSG00000228964.10","gene_symbol":"HLA-B","gene_name":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]","synonyms":"AS","biotype":"protein_coding","ncbi_id":"3106","summary":"HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]","start":31262912,"end":31350932,"strand":-1,"description":"major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]"}, {"versioned_ensembl_gene_id":"ENSG00000277876.1","gene_symbol":"AC108359.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30821815,"end":30823407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225403.1","gene_symbol":"WASF5P","gene_name":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]","synonyms":"Em:D84394.5","biotype":"processed_pseudogene","ncbi_id":"387122","summary":"This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":31281167,"end":31282618,"strand":-1,"description":"WAS protein family member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:21665]"}, {"versioned_ensembl_gene_id":"ENSG00000176601.12","gene_symbol":"MAP3K19","gene_name":"mitogen-activated protein kinase kinase kinase 19 [Source:HGNC Symbol;Acc:HGNC:26249]","synonyms":"YSK4,RCK,FLJ23074","biotype":"protein_coding","ncbi_id":"80122","summary":null,"start":134964491,"end":135047468,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 19 [Source:HGNC Symbol;Acc:HGNC:26249]"}, {"versioned_ensembl_gene_id":"ENSG00000257875.1","gene_symbol":"AC089998.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82468456,"end":82468948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250158.1","gene_symbol":"AC099509.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96247776,"end":96278751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213716.3","gene_symbol":"FABP5P5","gene_name":"fatty acid binding protein 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:31068]","synonyms":"FABP5L5","biotype":"processed_pseudogene","ncbi_id":"100288964","summary":null,"start":95973041,"end":95973446,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:31068]"}, {"versioned_ensembl_gene_id":"ENSG00000162009.8","gene_symbol":"SSTR5","gene_name":"somatostatin receptor 5 [Source:HGNC Symbol;Acc:HGNC:11334]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6755","summary":"Somatostatin and its related peptide cortistatin exert multiple biological actions on normal and tumoral tissue targets by interacting with somatostatin receptors (SSTRs). The protein encoded by this gene is one of the SSTRs, which is a multi-pass membrane protein and belongs to the G-protein coupled receptor 1 family. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase, and different regions of this receptor molecule are required for the activation of different signaling pathways. A mutation in this gene results in somatostatin analog resistance. Alternatively spliced transcript variants have been identified in this gene.[provided by RefSeq, Feb 2010]","start":1078781,"end":1080142,"strand":1,"description":"somatostatin receptor 5 [Source:HGNC Symbol;Acc:HGNC:11334]"}, {"versioned_ensembl_gene_id":"ENSG00000251254.1","gene_symbol":"GTF2F2P1","gene_name":"general transcription factor IIF subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4654]","synonyms":"TFIIF,GTF2F2L","biotype":"processed_pseudogene","ncbi_id":"2964","summary":null,"start":147506091,"end":147506765,"strand":1,"description":"general transcription factor IIF subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4654]"}, {"versioned_ensembl_gene_id":"ENSG00000144821.9","gene_symbol":"MYH15","gene_name":"myosin heavy chain 15 [Source:HGNC Symbol;Acc:HGNC:31073]","synonyms":"KIAA1000","biotype":"protein_coding","ncbi_id":"22989","summary":null,"start":108380369,"end":108529322,"strand":-1,"description":"myosin heavy chain 15 [Source:HGNC Symbol;Acc:HGNC:31073]"}, {"versioned_ensembl_gene_id":"ENSG00000243678.11","gene_symbol":"NME2","gene_name":"NME/NM23 nucleoside diphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:7850]","synonyms":"NM23-H2,NDPKB","biotype":"protein_coding","ncbi_id":"4831","summary":"Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by NME1) and 'B' (encoded by this gene) isoforms. Multiple alternatively spliced transcript variants have been found for this gene. Read-through transcription from the neighboring upstream gene (NME1) generates naturally-occurring transcripts (NME1-NME2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":51165435,"end":51171747,"strand":1,"description":"NME/NM23 nucleoside diphosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:7850]"}, {"versioned_ensembl_gene_id":"ENSG00000267637.1","gene_symbol":"AC040904.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":59784813,"end":59785035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110881.11","gene_symbol":"ASIC1","gene_name":"acid sensing ion channel subunit 1 [Source:HGNC Symbol;Acc:HGNC:100]","synonyms":"BNaC2,ACCN2,hBNaC2","biotype":"protein_coding","ncbi_id":"41","summary":"This gene encodes a member of the acid-sensing ion channel (ASIC) family of proteins, which are part of the degenerin/epithelial sodium channel (DEG/ENaC) superfamily. Members of the ASIC family are sensitive to amiloride and function in neurotransmission. The encoded proteins function in learning, pain transduction, touch sensation, and development of memory and fear. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]","start":50057548,"end":50083611,"strand":1,"description":"acid sensing ion channel subunit 1 [Source:HGNC Symbol;Acc:HGNC:100]"}, {"versioned_ensembl_gene_id":"ENSG00000086062.12","gene_symbol":"B4GALT1","gene_name":"beta-1,4-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:924]","synonyms":"GGTB2,beta4Gal-T1","biotype":"protein_coding","ncbi_id":"2683","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. This gene is unique among the beta4GalT genes because it encodes an enzyme that participates both in glycoconjugate and lactose biosynthesis. For the first activity, the enzyme adds galactose to N-acetylglucosamine residues that are either monosaccharides or the nonreducing ends of glycoprotein carbohydrate chains. The second activity is restricted to lactating mammary tissues where the enzyme forms a heterodimer with alpha-lactalbumin to catalyze UDP-galactose + D-glucose <=> UDP + lactose. The two enzymatic forms result from alternate transcription initiation sites and post-translational processing. Two transcripts, which differ only at the 5' end, with approximate lengths of 4.1 kb and 3.9 kb encode the same protein. The longer transcript encodes the type II membrane-bound, trans-Golgi resident protein involved in glycoconjugate biosynthesis. The shorter transcript encodes a protein which is cleaved to form the soluble lactose synthase. [provided by RefSeq, Jul 2008]","start":33104082,"end":33167356,"strand":-1,"description":"beta-1,4-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:924]"}, {"versioned_ensembl_gene_id":"ENSG00000262759.1","gene_symbol":"MRPS21P9","gene_name":"mitochondrial ribosomal protein S21 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:29756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359772","summary":null,"start":50450179,"end":50450725,"strand":-1,"description":"mitochondrial ribosomal protein S21 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:29756]"}, {"versioned_ensembl_gene_id":"ENSG00000132297.11","gene_symbol":"HHLA1","gene_name":"HERV-H LTR-associating 1 [Source:HGNC Symbol;Acc:HGNC:4904]","synonyms":"PLA2L","biotype":"protein_coding","ncbi_id":"10086","summary":null,"start":132061486,"end":132111159,"strand":-1,"description":"HERV-H LTR-associating 1 [Source:HGNC Symbol;Acc:HGNC:4904]"}, {"versioned_ensembl_gene_id":"ENSG00000236843.8","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30678308,"end":30681681,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000278776.1","gene_symbol":"AC171558.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21645163,"end":21646246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173357.12","gene_symbol":"AC007967.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8906224,"end":8916073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188451.8","gene_symbol":"SRP72P2","gene_name":"signal recognition particle 72 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31096]","synonyms":"dJ274L14.2","biotype":"processed_pseudogene","ncbi_id":"153932","summary":null,"start":158237336,"end":158242797,"strand":-1,"description":"signal recognition particle 72 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31096]"}, {"versioned_ensembl_gene_id":"ENSG00000146802.12","gene_symbol":"TMEM168","gene_name":"transmembrane protein 168 [Source:HGNC Symbol;Acc:HGNC:25826]","synonyms":"FLJ13576,DKFZp564C012","biotype":"protein_coding","ncbi_id":"64418","summary":null,"start":112762382,"end":112790592,"strand":-1,"description":"transmembrane protein 168 [Source:HGNC Symbol;Acc:HGNC:25826]"}, {"versioned_ensembl_gene_id":"ENSG00000277816.5","gene_symbol":"LILRB3","gene_name":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]","synonyms":"LIR-3,ILT5,PIRB,HL9,PIR-B,CD85a,LIR3","biotype":"protein_coding","ncbi_id":"11025","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54217107,"end":54223520,"strand":-1,"description":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]"}, {"versioned_ensembl_gene_id":"ENSG00000213514.2","gene_symbol":"AL731556.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77730766,"end":77734769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255343.1","gene_symbol":"AC234917.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":143833270,"end":143834063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198967.4","gene_symbol":"OR10Z1","gene_name":"olfactory receptor family 10 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:14996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128368","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158605268,"end":158612514,"strand":1,"description":"olfactory receptor family 10 subfamily Z member 1 [Source:HGNC Symbol;Acc:HGNC:14996]"}, {"versioned_ensembl_gene_id":"ENSG00000227813.1","gene_symbol":"Z82190.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31890344,"end":31891434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186912.6","gene_symbol":"P2RY4","gene_name":"pyrimidinergic receptor P2Y4 [Source:HGNC Symbol;Acc:HGNC:8542]","synonyms":"UNR,P2Y4,P2P,NRU","biotype":"protein_coding","ncbi_id":"5030","summary":"The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is responsive to uridine nucleotides, partially responsive to ATP, and not responsive to ADP. [provided by RefSeq, Jul 2008]","start":70258170,"end":70259764,"strand":-1,"description":"pyrimidinergic receptor P2Y4 [Source:HGNC Symbol;Acc:HGNC:8542]"}, {"versioned_ensembl_gene_id":"ENSG00000240254.1","gene_symbol":"B4GALT4-AS1","gene_name":"B4GALT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40090]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874201","summary":null,"start":119226486,"end":119290666,"strand":1,"description":"B4GALT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40090]"}, {"versioned_ensembl_gene_id":"ENSG00000182747.4","gene_symbol":"SLC35D3","gene_name":"solute carrier family 35 member D3 [Source:HGNC Symbol;Acc:HGNC:15621]","synonyms":"FRCL1","biotype":"protein_coding","ncbi_id":"340146","summary":null,"start":136922264,"end":136925639,"strand":1,"description":"solute carrier family 35 member D3 [Source:HGNC Symbol;Acc:HGNC:15621]"}, {"versioned_ensembl_gene_id":"ENSG00000197006.13","gene_symbol":"METTL9","gene_name":"methyltransferase like 9 [Source:HGNC Symbol;Acc:HGNC:24586]","synonyms":"DREV1","biotype":"protein_coding","ncbi_id":"51108","summary":null,"start":21597218,"end":21657473,"strand":1,"description":"methyltransferase like 9 [Source:HGNC Symbol;Acc:HGNC:24586]"}, {"versioned_ensembl_gene_id":"ENSG00000197532.2","gene_symbol":"OR6Y1","gene_name":"olfactory receptor family 6 subfamily Y member 1 [Source:HGNC Symbol;Acc:HGNC:14823]","synonyms":"OR6Y2","biotype":"protein_coding","ncbi_id":"391112","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158544550,"end":158554405,"strand":-1,"description":"olfactory receptor family 6 subfamily Y member 1 [Source:HGNC Symbol;Acc:HGNC:14823]"}, {"versioned_ensembl_gene_id":"ENSG00000282695.1","gene_symbol":"HMGB1P24","gene_name":"high mobility group box 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39115]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100420063","summary":null,"start":37145064,"end":37145920,"strand":-1,"description":"high mobility group box 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39115]"}, {"versioned_ensembl_gene_id":"ENSG00000255259.2","gene_symbol":"ZNF123P","gene_name":"zinc finger protein 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:12906]","synonyms":"ZNF123,HZF-1","biotype":"processed_pseudogene","ncbi_id":"100188891","summary":null,"start":129295286,"end":129296481,"strand":-1,"description":"zinc finger protein 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:12906]"}, {"versioned_ensembl_gene_id":"ENSG00000025039.14","gene_symbol":"RRAGD","gene_name":"Ras related GTP binding D [Source:HGNC Symbol;Acc:HGNC:19903]","synonyms":"DKFZP761H171,bA11D8.2.1","biotype":"protein_coding","ncbi_id":"58528","summary":"RRAGD is a monomeric guanine nucleotide-binding protein, or G protein. By binding GTP or GDP, small G proteins act as molecular switches in numerous cell processes and signaling pathways.[supplied by OMIM, Apr 2004]","start":89364636,"end":89412270,"strand":-1,"description":"Ras related GTP binding D [Source:HGNC Symbol;Acc:HGNC:19903]"}, {"versioned_ensembl_gene_id":"ENSG00000167311.13","gene_symbol":"ART5","gene_name":"ADP-ribosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:24049]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116969","summary":"The protein encoded by this gene belongs to the ARG-specific ADP-ribosyltransferase family. Proteins in this family regulate the function of target proteins by attaching ADP-ribose to specific amino acid residues in their target proteins. The mouse homolog lacks a glycosylphosphatidylinositol-anchor signal sequence and is predicted to be a secretory enzyme. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":3638503,"end":3642316,"strand":-1,"description":"ADP-ribosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:24049]"}, {"versioned_ensembl_gene_id":"ENSG00000224738.1","gene_symbol":"AC099850.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59106598,"end":59118267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263938.1","gene_symbol":"AC100832.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58965952,"end":58966727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233814.1","gene_symbol":"AL590664.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76419934,"end":76420631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261236.7","gene_symbol":"BOP1","gene_name":"block of proliferation 1 [Source:HGNC Symbol;Acc:HGNC:15519]","synonyms":"KIAA0124","biotype":"protein_coding","ncbi_id":"23246","summary":null,"start":144262102,"end":144291370,"strand":-1,"description":"block of proliferation 1 [Source:HGNC Symbol;Acc:HGNC:15519]"}, {"versioned_ensembl_gene_id":"ENSG00000259619.2","gene_symbol":"AC010867.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54048588,"end":54050876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237976.1","gene_symbol":"AL391069.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151346967,"end":151348027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224674.1","gene_symbol":"EIF3EP2","gene_name":"eukaryotic translation initiation factor 3 subunit E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132597","summary":null,"start":162088259,"end":162090072,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37919]"}, {"versioned_ensembl_gene_id":"ENSG00000224645.1","gene_symbol":"AL391069.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151340648,"end":151341966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089639.10","gene_symbol":"GMIP","gene_name":"GEM interacting protein [Source:HGNC Symbol;Acc:HGNC:24852]","synonyms":"ARHGAP46","biotype":"protein_coding","ncbi_id":"51291","summary":"This gene encodes a member of the ARHGAP family of Rho/Rac/Cdc42-like GTPase activating proteins. The encoded protein interacts with the Ras-related protein Gem through its N-terminal domain. Separately, it interacts with RhoA through a RhoGAP domain, and stimulates RhoA-dependent GTPase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":19629476,"end":19643667,"strand":-1,"description":"GEM interacting protein [Source:HGNC Symbol;Acc:HGNC:24852]"}, {"versioned_ensembl_gene_id":"ENSG00000188467.10","gene_symbol":"SLC24A5","gene_name":"solute carrier family 24 member 5 [Source:HGNC Symbol;Acc:HGNC:20611]","synonyms":"OCA6,JSX","biotype":"protein_coding","ncbi_id":"283652","summary":"This gene is a member of the potassium-dependent sodium/calcium exchanger family and encodes an intracellular membrane protein with 2 large hydrophilic loops and 2 sets of multiple transmembrane-spanning segments. Sequence variation in this gene has been associated with differences in skin pigmentation. [provided by RefSeq, Jul 2008]","start":48120972,"end":48142672,"strand":1,"description":"solute carrier family 24 member 5 [Source:HGNC Symbol;Acc:HGNC:20611]"}, {"versioned_ensembl_gene_id":"ENSG00000226145.7","gene_symbol":"KRT16P6","gene_name":"keratin 16 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50719]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"353194","summary":null,"start":16817983,"end":16822579,"strand":-1,"description":"keratin 16 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50719]"}, {"versioned_ensembl_gene_id":"ENSG00000248996.1","gene_symbol":"AC145098.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177494995,"end":177503647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271022.1","gene_symbol":"AP002365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121426645,"end":121427416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233943.1","gene_symbol":"AC114973.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56975593,"end":56976224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234193.1","gene_symbol":"AC013476.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":222917387,"end":222919363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284633.1","gene_symbol":"AL031590.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39242188,"end":39279897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206298.8","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32769412,"end":32773398,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000232289.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425576,"end":29457138,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000259788.1","gene_symbol":"AL596325.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":162560227,"end":162561308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229184.2","gene_symbol":"ATP5HP2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49624]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"138234","summary":null,"start":2900320,"end":2900804,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49624]"}, {"versioned_ensembl_gene_id":"ENSG00000243574.1","gene_symbol":"AC006148.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124274679,"end":124287544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243055.1","gene_symbol":"GK-AS1","gene_name":"GK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40255]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873902","summary":null,"start":30699998,"end":30724174,"strand":-1,"description":"GK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40255]"}, {"versioned_ensembl_gene_id":"ENSG00000273262.1","gene_symbol":"AL121928.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102483039,"end":102483559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238071.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31532567,"end":31533401,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000272239.1","gene_symbol":"AC011373.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147401760,"end":147401996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047662.4","gene_symbol":"FAM184B","gene_name":"family with sequence similarity 184 member B [Source:HGNC Symbol;Acc:HGNC:29235]","synonyms":"KIAA1276","biotype":"protein_coding","ncbi_id":"27146","summary":null,"start":17629306,"end":17781512,"strand":-1,"description":"family with sequence similarity 184 member B [Source:HGNC Symbol;Acc:HGNC:29235]"}, {"versioned_ensembl_gene_id":"ENSG00000267517.1","gene_symbol":"LINC01855","gene_name":"long intergenic non-protein coding RNA 1855 [Source:HGNC Symbol;Acc:HGNC:52675]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372292","summary":null,"start":16065737,"end":16066312,"strand":1,"description":"long intergenic non-protein coding RNA 1855 [Source:HGNC Symbol;Acc:HGNC:52675]"}, {"versioned_ensembl_gene_id":"ENSG00000279821.1","gene_symbol":"AC145098.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":177476631,"end":177479656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206445.4","gene_symbol":"ATP6V1G2","gene_name":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]","synonyms":"ATP6G,Em:AC004181.3,Vma10,ATP6G2,NG38","biotype":"protein_coding","ncbi_id":"534","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of three V1 domain G subunit proteins. This gene had previous gene symbols of ATP6G and ATP6G2. Alternatively spliced transcript variants encoding different isoforms have been described. Read-through transcription also exists between this gene and the downstream DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B) gene. [provided by RefSeq, Feb 2011]","start":31534725,"end":31537107,"strand":-1,"description":"ATPase H+ transporting V1 subunit G2 [Source:HGNC Symbol;Acc:HGNC:862]"}, {"versioned_ensembl_gene_id":"ENSG00000275643.1","gene_symbol":"RBM22P6","gene_name":"RNA binding motif protein 22 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39699]","synonyms":"RBM22P10","biotype":"processed_pseudogene","ncbi_id":"644509","summary":null,"start":52485046,"end":52485912,"strand":-1,"description":"RNA binding motif protein 22 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39699]"}, {"versioned_ensembl_gene_id":"ENSG00000112701.17","gene_symbol":"SENP6","gene_name":"SUMO1/sentrin specific peptidase 6 [Source:HGNC Symbol;Acc:HGNC:20944]","synonyms":"SUSP1,KIAA0797","biotype":"protein_coding","ncbi_id":"26054","summary":"Ubiquitin-like molecules (UBLs), such as SUMO1 (UBL1; MIM 601912), are structurally related to ubiquitin (MIM 191339) and can be ligated to target proteins in a similar manner as ubiquitin. However, covalent attachment of UBLs does not result in degradation of the modified proteins. SUMO1 modification is implicated in the targeting of RANGAP1 (MIM 602362) to the nuclear pore complex, as well as in stabilization of I-kappa-B-alpha (NFKBIA; MIM 164008) from degradation by the 26S proteasome. Like ubiquitin, UBLs are synthesized as precursor proteins, with 1 or more amino acids following the C-terminal glycine-glycine residues of the mature UBL protein. Thus, the tail sequences of the UBL precursors need to be removed by UBL-specific proteases, such as SENP6, prior to their conjugation to target proteins (Kim et al., 2000 [PubMed 10799485]). SENPs also display isopeptidase activity for deconjugation of SUMO-conjugated substrates (Lima and Reverter, 2008 [PubMed 18799455]).[supplied by OMIM, Jun 2009]","start":75601509,"end":75718278,"strand":1,"description":"SUMO1/sentrin specific peptidase 6 [Source:HGNC Symbol;Acc:HGNC:20944]"}, {"versioned_ensembl_gene_id":"ENSG00000115084.13","gene_symbol":"SLC35F5","gene_name":"solute carrier family 35 member F5 [Source:HGNC Symbol;Acc:HGNC:23617]","synonyms":"FLJ22004","biotype":"protein_coding","ncbi_id":"80255","summary":null,"start":113705011,"end":113756823,"strand":-1,"description":"solute carrier family 35 member F5 [Source:HGNC Symbol;Acc:HGNC:23617]"}, {"versioned_ensembl_gene_id":"ENSG00000231927.1","gene_symbol":"AC093734.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1508655,"end":1509427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232837.1","gene_symbol":"LINC01700","gene_name":"long intergenic non-protein coding RNA 1700 [Source:HGNC Symbol;Acc:HGNC:52488]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928435","summary":null,"start":38974429,"end":38977774,"strand":-1,"description":"long intergenic non-protein coding RNA 1700 [Source:HGNC Symbol;Acc:HGNC:52488]"}, {"versioned_ensembl_gene_id":"ENSG00000235811.1","gene_symbol":"AL691482.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":202039851,"end":202039934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240423.1","gene_symbol":"LINC00636","gene_name":"long intergenic non-protein coding RNA 636 [Source:HGNC Symbol;Acc:HGNC:27702]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285205","summary":null,"start":107883248,"end":107928907,"strand":1,"description":"long intergenic non-protein coding RNA 636 [Source:HGNC Symbol;Acc:HGNC:27702]"}, {"versioned_ensembl_gene_id":"ENSG00000106304.15","gene_symbol":"SPAM1","gene_name":"sperm adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:11217]","synonyms":"SPAG15,PH-20,HYAL5","biotype":"protein_coding","ncbi_id":"6677","summary":"Hyaluronidase degrades hyaluronic acid, a major structural proteoglycan found in extracellular matrices and basement membranes. Six members of the hyaluronidase family are clustered into two tightly linked groups on chromosome 3p21.3 and 7q31.3. This gene was previously referred to as HYAL1 and HYA1 and has since been assigned the official symbol SPAM1; another family member on chromosome 3p21.3 has been assigned HYAL1. This gene encodes a GPI-anchored enzyme located on the human sperm surface and inner acrosomal membrane. This multifunctional protein is a hyaluronidase that enables sperm to penetrate through the hyaluronic acid-rich cumulus cell layer surrounding the oocyte, a receptor that plays a role in hyaluronic acid induced cell signaling, and a receptor that is involved in sperm-zona pellucida adhesion. Abnormal expression of this gene in tumors has implicated this protein in degradation of basement membranes leading to tumor invasion and metastasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":123925237,"end":123971414,"strand":1,"description":"sperm adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:11217]"}, {"versioned_ensembl_gene_id":"ENSG00000241345.1","gene_symbol":"AC004690.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123994622,"end":124027659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225583.1","gene_symbol":"AC004690.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123932132,"end":123932459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259720.1","gene_symbol":"AC009562.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31002013,"end":31042302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259045.1","gene_symbol":"MTCO1P2","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19932]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"326603","summary":null,"start":32484098,"end":32484800,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19932]"}, {"versioned_ensembl_gene_id":"ENSG00000169375.15","gene_symbol":"SIN3A","gene_name":"SIN3 transcription regulator family member A [Source:HGNC Symbol;Acc:HGNC:19353]","synonyms":"KIAA0700,DKFZP434K2235","biotype":"protein_coding","ncbi_id":"25942","summary":"The protein encoded by this gene is a transcriptional regulatory protein. It contains paired amphipathic helix (PAH) domains, which are important for protein-protein interactions and may mediate repression by the Mad-Max complex. [provided by RefSeq, Jul 2008]","start":75369379,"end":75455842,"strand":-1,"description":"SIN3 transcription regulator family member A [Source:HGNC Symbol;Acc:HGNC:19353]"}, {"versioned_ensembl_gene_id":"ENSG00000185697.16","gene_symbol":"MYBL1","gene_name":"MYB proto-oncogene like 1 [Source:HGNC Symbol;Acc:HGNC:7547]","synonyms":"AMYB,A-myb","biotype":"protein_coding","ncbi_id":"4603","summary":null,"start":66562175,"end":66614247,"strand":-1,"description":"MYB proto-oncogene like 1 [Source:HGNC Symbol;Acc:HGNC:7547]"}, {"versioned_ensembl_gene_id":"ENSG00000168967.14","gene_symbol":"PMCHL1","gene_name":"pro-melanin concentrating hormone like 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9110]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5369","summary":null,"start":22142352,"end":22152356,"strand":1,"description":"pro-melanin concentrating hormone like 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9110]"}, {"versioned_ensembl_gene_id":"ENSG00000130643.8","gene_symbol":"CALY","gene_name":"calcyon neuron specific vesicular protein [Source:HGNC Symbol;Acc:HGNC:17938]","synonyms":"NSG3,DRD1IP,CALCYON","biotype":"protein_coding","ncbi_id":"50632","summary":"The protein encoded by this gene is a type II single transmembrane protein. It is required for maximal stimulated calcium release after stimulation of purinergic or muscarinic but not beta-adrenergic receptors. The encoded protein interacts with D1 dopamine receptor and may interact with other DA receptor subtypes and/or GPCRs. [provided by RefSeq, Jul 2008]","start":133324072,"end":133336935,"strand":-1,"description":"calcyon neuron specific vesicular protein [Source:HGNC Symbol;Acc:HGNC:17938]"}, {"versioned_ensembl_gene_id":"ENSG00000108829.9","gene_symbol":"LRRC59","gene_name":"leucine rich repeat containing 59 [Source:HGNC Symbol;Acc:HGNC:28817]","synonyms":"PRO1855,FLJ21675","biotype":"protein_coding","ncbi_id":"55379","summary":null,"start":50375059,"end":50397553,"strand":-1,"description":"leucine rich repeat containing 59 [Source:HGNC Symbol;Acc:HGNC:28817]"}, {"versioned_ensembl_gene_id":"ENSG00000169084.13","gene_symbol":"DHRSX","gene_name":"dehydrogenase/reductase X-linked [Source:HGNC Symbol;Acc:HGNC:18399]","synonyms":"SDR7C6,SDR46C1,DHRSY,DHRSXY,DHRS5Y,DHRS5X","biotype":"protein_coding","ncbi_id":"207063","summary":null,"start":2219516,"end":2502805,"strand":-1,"description":"dehydrogenase/reductase X-linked [Source:HGNC Symbol;Acc:HGNC:18399]"}, {"versioned_ensembl_gene_id":"ENSG00000267059.2","gene_symbol":"AC005943.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1578339,"end":1605445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108826.15","gene_symbol":"MRPL27","gene_name":"mitochondrial ribosomal protein L27 [Source:HGNC Symbol;Acc:HGNC:14483]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51264","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":50367857,"end":50373214,"strand":-1,"description":"mitochondrial ribosomal protein L27 [Source:HGNC Symbol;Acc:HGNC:14483]"}, {"versioned_ensembl_gene_id":"ENSG00000274667.1","gene_symbol":"AC090517.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56729932,"end":56730611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271830.1","gene_symbol":"AC012213.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103481266,"end":103481619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255189.1","gene_symbol":"GLYATL1P1","gene_name":"glycine-N-acyltransferase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37866]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129032","summary":null,"start":58978787,"end":58994120,"strand":1,"description":"glycine-N-acyltransferase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37866]"}, {"versioned_ensembl_gene_id":"ENSG00000258619.2","gene_symbol":"AL136298.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32241524,"end":32243093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274338.2","gene_symbol":"CATSPERB","gene_name":"cation channel sperm associated auxiliary subunit beta [Source:HGNC Symbol;Acc:HGNC:20500]","synonyms":"FLJ14298,C14orf161","biotype":"protein_coding","ncbi_id":"79820","summary":null,"start":91580696,"end":91784366,"strand":-1,"description":"cation channel sperm associated auxiliary subunit beta [Source:HGNC Symbol;Acc:HGNC:20500]"}, {"versioned_ensembl_gene_id":"ENSG00000145780.7","gene_symbol":"FEM1C","gene_name":"fem-1 homolog C [Source:HGNC Symbol;Acc:HGNC:16933]","synonyms":"KIAA1785,FEM1A,EUROIMAGE783647,EUROIMAGE686608","biotype":"protein_coding","ncbi_id":"56929","summary":null,"start":115520908,"end":115544894,"strand":-1,"description":"fem-1 homolog C [Source:HGNC Symbol;Acc:HGNC:16933]"}, {"versioned_ensembl_gene_id":"ENSG00000166153.16","gene_symbol":"DEPDC4","gene_name":"DEP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:22952]","synonyms":"FLJ33505,DEP.4","biotype":"protein_coding","ncbi_id":"120863","summary":null,"start":100203669,"end":100267079,"strand":-1,"description":"DEP domain containing 4 [Source:HGNC Symbol;Acc:HGNC:22952]"}, {"versioned_ensembl_gene_id":"ENSG00000250444.1","gene_symbol":"CCT5P1","gene_name":"chaperonin containing TCP1 subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35135]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402226","summary":null,"start":115512077,"end":115513694,"strand":1,"description":"chaperonin containing TCP1 subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35135]"}, {"versioned_ensembl_gene_id":"ENSG00000281924.1","gene_symbol":"POLR3GP1","gene_name":"RNA polymerase III subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23345]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100422395","summary":null,"start":91603173,"end":91603433,"strand":-1,"description":"RNA polymerase III subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23345]"}, {"versioned_ensembl_gene_id":"ENSG00000237849.1","gene_symbol":"NFYAP1","gene_name":"nuclear transcription factor Y subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34078]","synonyms":"NFYAP","biotype":"processed_pseudogene","ncbi_id":"100130677","summary":null,"start":63975451,"end":63976422,"strand":-1,"description":"nuclear transcription factor Y subunit alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34078]"}, {"versioned_ensembl_gene_id":"ENSG00000102531.16","gene_symbol":"FNDC3A","gene_name":"fibronectin type III domain containing 3A [Source:HGNC Symbol;Acc:HGNC:20296]","synonyms":"KIAA0970,FNDC3,bA203I16.5","biotype":"protein_coding","ncbi_id":"22862","summary":null,"start":48975912,"end":49209779,"strand":1,"description":"fibronectin type III domain containing 3A [Source:HGNC Symbol;Acc:HGNC:20296]"}, {"versioned_ensembl_gene_id":"ENSG00000223529.1","gene_symbol":"EEF1A1P8","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3203]","synonyms":"EEF1AL6","biotype":"processed_pseudogene","ncbi_id":"389179","summary":null,"start":184026369,"end":184027756,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:3203]"}, {"versioned_ensembl_gene_id":"ENSG00000228951.1","gene_symbol":"AL365356.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5616862,"end":5618161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174156.14","gene_symbol":"GSTA3","gene_name":"glutathione S-transferase alpha 3 [Source:HGNC Symbol;Acc:HGNC:4628]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2940","summary":"Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. These enzymes are involved in cellular defense against toxic, carcinogenic, and pharmacologically active electrophilic compounds. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-tranferase belonging to the alpha class genes that are located in a cluster mapped to chromosome 6. Genes of the alpha class are highly related and encode enzymes with glutathione peroxidase activity. However, during evolution, this alpha class gene diverged accumulating mutations in the active site that resulted in differences in substrate specificity and catalytic activity. The enzyme encoded by this gene catalyzes the double bond isomerization of precursors for progesterone and testosterone during the biosynthesis of steroid hormones. An additional transcript variant has been identified, but its full length sequence has not been determined. [provided by RefSeq, Jul 2008]","start":52896639,"end":52909685,"strand":-1,"description":"glutathione S-transferase alpha 3 [Source:HGNC Symbol;Acc:HGNC:4628]"}, {"versioned_ensembl_gene_id":"ENSG00000152207.7","gene_symbol":"CYSLTR2","gene_name":"cysteinyl leukotriene receptor 2 [Source:HGNC Symbol;Acc:HGNC:18274]","synonyms":"CYSLT2R,CysLT(2)","biotype":"protein_coding","ncbi_id":"57105","summary":"The cysteinyl leukotrienes LTC4, LTD4, and LTE4 are important mediators of human bronchial asthma. Pharmacologic studies have determined that cysteinyl leukotrienes activate at least 2 receptors, the protein encoded by this gene and CYSLTR1. This encoded receptor is a member of the superfamily of G protein-coupled receptors. It seems to play a major role in endocrine and cardiovascular systems. [provided by RefSeq, Jul 2008]","start":48653711,"end":48711226,"strand":1,"description":"cysteinyl leukotriene receptor 2 [Source:HGNC Symbol;Acc:HGNC:18274]"}, {"versioned_ensembl_gene_id":"ENSG00000229836.1","gene_symbol":"AL671883.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31307815,"end":31308549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214892.4","gene_symbol":"USP8P1","gene_name":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]","synonyms":"D84394.7,USP8P,KIAA0055-hom","biotype":"processed_pseudogene","ncbi_id":"100287272","summary":null,"start":31275572,"end":31278754,"strand":1,"description":"ubiquitin specific peptidase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13987]"}, {"versioned_ensembl_gene_id":"ENSG00000075089.9","gene_symbol":"ACTR6","gene_name":"ARP6 actin related protein 6 homolog [Source:HGNC Symbol;Acc:HGNC:24025]","synonyms":"FLJ13433,ARP6","biotype":"protein_coding","ncbi_id":"64431","summary":null,"start":100199122,"end":100241865,"strand":1,"description":"ARP6 actin related protein 6 homolog [Source:HGNC Symbol;Acc:HGNC:24025]"}, {"versioned_ensembl_gene_id":"ENSG00000213117.4","gene_symbol":"AL021939.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134897874,"end":134898759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158715.5","gene_symbol":"SLC45A3","gene_name":"solute carrier family 45 member 3 [Source:HGNC Symbol;Acc:HGNC:8642]","synonyms":"prostein,PCANAP8,PCANAP6,PCANAP2,IPCA-8,IPCA-6,IPCA-2","biotype":"protein_coding","ncbi_id":"85414","summary":null,"start":205657851,"end":205680459,"strand":-1,"description":"solute carrier family 45 member 3 [Source:HGNC Symbol;Acc:HGNC:8642]"}, {"versioned_ensembl_gene_id":"ENSG00000248286.1","gene_symbol":"AC140172.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21196720,"end":21196860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235461.1","gene_symbol":"AC003001.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85210706,"end":85219698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129538.13","gene_symbol":"RNASE1","gene_name":"ribonuclease A family member 1, pancreatic [Source:HGNC Symbol;Acc:HGNC:10044]","synonyms":"RNS1,RAC1","biotype":"protein_coding","ncbi_id":"6035","summary":"This gene encodes a member of the pancreatic-type of secretory ribonucleases, a subset of the ribonuclease A superfamily. The encoded endonuclease cleaves internal phosphodiester RNA bonds on the 3'-side of pyrimidine bases. It prefers poly(C) as a substrate and hydrolyzes 2',3'-cyclic nucleotides, with a pH optimum near 8.0. The encoded protein is monomeric and more commonly acts to degrade ds-RNA over ss-RNA. Alternative splicing occurs at this locus and four transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":20801228,"end":20803278,"strand":-1,"description":"ribonuclease A family member 1, pancreatic [Source:HGNC Symbol;Acc:HGNC:10044]"}, {"versioned_ensembl_gene_id":"ENSG00000276391.1","gene_symbol":"AC003001.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85207187,"end":85210649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176540.3","gene_symbol":"OR4C5","gene_name":"olfactory receptor family 4 subfamily C member 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14702]","synonyms":"OR4C5Q,OR4C5P","biotype":"protein_coding","ncbi_id":"79346","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":48365485,"end":48366465,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 5 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14702]"}, {"versioned_ensembl_gene_id":"ENSG00000057149.15","gene_symbol":"SERPINB3","gene_name":"serpin family B member 3 [Source:HGNC Symbol;Acc:HGNC:10569]","synonyms":"T4-A,SCCA1,SCC,HsT1196","biotype":"protein_coding","ncbi_id":"6317","summary":null,"start":63655197,"end":63661963,"strand":-1,"description":"serpin family B member 3 [Source:HGNC Symbol;Acc:HGNC:10569]"}, {"versioned_ensembl_gene_id":"ENSG00000151665.12","gene_symbol":"PIGF","gene_name":"phosphatidylinositol glycan anchor biosynthesis class F [Source:HGNC Symbol;Acc:HGNC:8962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5281","summary":"This gene encodes a protein involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor, a glycolipid containing three mannose molecules in its core backbone, is found on many blood cells where it serves to anchor proteins to the cell surface. The encoded protein and another GPI synthesis protein, PIGO, function in the transfer of ethanolaminephosphate to the third mannose in GPI. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":46580937,"end":46617119,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class F [Source:HGNC Symbol;Acc:HGNC:8962]"}, {"versioned_ensembl_gene_id":"ENSG00000181552.3","gene_symbol":"EDDM3B","gene_name":"epididymal protein 3B [Source:HGNC Symbol;Acc:HGNC:19223]","synonyms":"HE3-BETA,FAM12B","biotype":"protein_coding","ncbi_id":"64184","summary":"Testicular sperm are morphologically differentiated but are not progressively motile nor able to fertilize an egg. Post-testicular maturation requires exposure of spermatozoa to the microenvironment of the epididymal lumen. Spermatozoa undergo extensive changes in the epididymis, including enzymatic modifications, loss of pre-existing components and addition of new glycoproteins from epididymal secretions. These modifying proteins and enzymes are synthesized by epithelial cells lining the epididymal duct and secreted apically into the lumen, where they come into contact with, and may be absorbed onto, the sperm membranes. The proteins encoded by the genes in this cluster are synthesized and secreted by epididymal epithelial cells. [provided by RefSeq, Jul 2008]","start":20768427,"end":20770948,"strand":1,"description":"epididymal protein 3B [Source:HGNC Symbol;Acc:HGNC:19223]"}, {"versioned_ensembl_gene_id":"ENSG00000258316.1","gene_symbol":"KLF17P1","gene_name":"Kruppel like factor 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41521]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133321","summary":null,"start":62234390,"end":62235515,"strand":-1,"description":"Kruppel like factor 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41521]"}, {"versioned_ensembl_gene_id":"ENSG00000270706.1","gene_symbol":"PRMT1P1","gene_name":"protein arginine methyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420910","summary":null,"start":177265580,"end":177266588,"strand":-1,"description":"protein arginine methyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49611]"}, {"versioned_ensembl_gene_id":"ENSG00000234710.1","gene_symbol":"AC060834.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9737322,"end":9769513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242990.2","gene_symbol":"RPL13AP23","gene_name":"ribosomal protein L13a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441641","summary":null,"start":57674665,"end":57675250,"strand":1,"description":"ribosomal protein L13a pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36498]"}, {"versioned_ensembl_gene_id":"ENSG00000269524.1","gene_symbol":"AC245052.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54224523,"end":54224881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157881.13","gene_symbol":"PANK4","gene_name":"pantothenate kinase 4 [Source:HGNC Symbol;Acc:HGNC:19366]","synonyms":"FLJ10782","biotype":"protein_coding","ncbi_id":"55229","summary":"This gene encodes a protein belonging to the pantothenate kinase family. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by CoA. This family member is most abundant in muscle but is expressed in all tissues. [provided by RefSeq, Jul 2008]","start":2508533,"end":2526628,"strand":-1,"description":"pantothenate kinase 4 [Source:HGNC Symbol;Acc:HGNC:19366]"}, {"versioned_ensembl_gene_id":"ENSG00000205649.7","gene_symbol":"HTN3","gene_name":"histatin 3 [Source:HGNC Symbol;Acc:HGNC:5284]","synonyms":"HIS2","biotype":"protein_coding","ncbi_id":"3347","summary":"This gene encodes a member of the histatin family of small, histidine-rich, cationic proteins. They function as antimicrobial peptides and are important components of the innate immune system. Histatins are found in saliva and exhibit antibacterial, antifungal activities and function in wound healing. [provided by RefSeq, Sep 2014]","start":70028413,"end":70036538,"strand":1,"description":"histatin 3 [Source:HGNC Symbol;Acc:HGNC:5284]"}, {"versioned_ensembl_gene_id":"ENSG00000253964.1","gene_symbol":"AC103783.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68293446,"end":68293818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128973.12","gene_symbol":"CLN6","gene_name":"CLN6, transmembrane ER protein [Source:HGNC Symbol;Acc:HGNC:2077]","synonyms":"nclf,HsT18960,FLJ20561","biotype":"protein_coding","ncbi_id":"54982","summary":"This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. [provided by RefSeq, Oct 2008]","start":68206992,"end":68257211,"strand":-1,"description":"CLN6, transmembrane ER protein [Source:HGNC Symbol;Acc:HGNC:2077]"}, {"versioned_ensembl_gene_id":"ENSG00000248542.2","gene_symbol":"AC233724.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17649046,"end":17649643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234892.1","gene_symbol":"Z82214.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43232141,"end":43239010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255096.2","gene_symbol":"OR5B10P","gene_name":"olfactory receptor family 5 subfamily B member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:8320]","synonyms":"OR13-34,OR5B4P,OR5B18P,OR5B11P,OR5B11,OR5B10,OR13-67,OR13-64","biotype":"unprocessed_pseudogene","ncbi_id":"390186","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":58348989,"end":58349630,"strand":-1,"description":"olfactory receptor family 5 subfamily B member 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:8320]"}, {"versioned_ensembl_gene_id":"ENSG00000181171.5","gene_symbol":"FER1L6-AS1","gene_name":"FER1L6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26652]","synonyms":"FLJ35721,C8orf54","biotype":"antisense_RNA","ncbi_id":"439941","summary":null,"start":123984138,"end":124040782,"strand":-1,"description":"FER1L6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26652]"}, {"versioned_ensembl_gene_id":"ENSG00000148848.14","gene_symbol":"ADAM12","gene_name":"ADAM metallopeptidase domain 12 [Source:HGNC Symbol;Acc:HGNC:190]","synonyms":"MLTN,MCMPMltna","biotype":"protein_coding","ncbi_id":"8038","summary":"This gene encodes a member of a family of proteins that are structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. Expression of this gene has been used as a maternal serum marker for pre-natal development. Alternative splicing results in multiple transcript variants encoding different isoforms. Shorter isoforms are secreted, while longer isoforms are membrane-bound form. [provided by RefSeq, Jan 2014]","start":126012381,"end":126388455,"strand":-1,"description":"ADAM metallopeptidase domain 12 [Source:HGNC Symbol;Acc:HGNC:190]"}, {"versioned_ensembl_gene_id":"ENSG00000172551.10","gene_symbol":"MUCL1","gene_name":"mucin like 1 [Source:HGNC Symbol;Acc:HGNC:30588]","synonyms":"SBEM","biotype":"protein_coding","ncbi_id":"118430","summary":null,"start":54830519,"end":54858393,"strand":1,"description":"mucin like 1 [Source:HGNC Symbol;Acc:HGNC:30588]"}, {"versioned_ensembl_gene_id":"ENSG00000241030.1","gene_symbol":"AC063943.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120522664,"end":120523443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113648.16","gene_symbol":"H2AFY","gene_name":"H2A histone family member Y [Source:HGNC Symbol;Acc:HGNC:4740]","synonyms":"macroH2A1.2","biotype":"protein_coding","ncbi_id":"9555","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. It replaces conventional H2A histones in a subset of nucleosomes where it represses transcription and participates in stable X chromosome inactivation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]","start":135333900,"end":135399914,"strand":-1,"description":"H2A histone family member Y [Source:HGNC Symbol;Acc:HGNC:4740]"}, {"versioned_ensembl_gene_id":"ENSG00000148154.9","gene_symbol":"UGCG","gene_name":"UDP-glucose ceramide glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:12524]","synonyms":"GCS","biotype":"protein_coding","ncbi_id":"7357","summary":"This gene encodes an enzyme that catalyzes the first glycosylation step in the biosynthesis of glycosphingolipids, which are membrane components containing lipid and sugar moieties. The product of this reaction is glucosylceramide, which is the core structure of many glycosphingolipids. [provided by RefSeq, Dec 2014]","start":111896766,"end":111935369,"strand":1,"description":"UDP-glucose ceramide glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:12524]"}, {"versioned_ensembl_gene_id":"ENSG00000223501.8","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"SACM2L,ARE1","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33250272,"end":33272047,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000231147.2","gene_symbol":"ARHGAP42P2","gene_name":"Rho GTPase activating protein 42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43939]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130693","summary":null,"start":130006200,"end":130009123,"strand":1,"description":"Rho GTPase activating protein 42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43939]"}, {"versioned_ensembl_gene_id":"ENSG00000280375.1","gene_symbol":"AL359740.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74122134,"end":74122725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234571.1","gene_symbol":"AC239798.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143877731,"end":143885076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282166.1","gene_symbol":"AC003103.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37047293,"end":37054608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225011.4","gene_symbol":"AL671862.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29488193,"end":29496893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244682.7","gene_symbol":"FCGR2C","gene_name":"Fc fragment of IgG receptor IIc (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15626]","synonyms":"hFcRII-C,CD32C","biotype":"polymorphic_pseudogene","ncbi_id":"9103","summary":"This gene encodes one of three members of a family of low-affinity immunoglobulin gamma Fc receptors found on the surface of many immune response cells. The encoded protein is a transmembrane glycoprotein and may be involved in phagocytosis and clearing of immune complexes. An allelic polymorphism in this gene results in both coding and non-coding variants. [provided by RefSeq, Apr 2012]","start":161581339,"end":161605662,"strand":1,"description":"Fc fragment of IgG receptor IIc (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15626]"}, {"versioned_ensembl_gene_id":"ENSG00000003987.13","gene_symbol":"MTMR7","gene_name":"myotubularin related protein 7 [Source:HGNC Symbol;Acc:HGNC:7454]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9108","summary":"This gene encodes a member of the myotubularin family of tyrosine/dual-specificity phosphatases. The encoded protein is characterized by four distinct domains that are conserved among all members of the myotubularin family: the glucosyltransferase, Rab-like GTPase activator and myotubularins domain, the Rac-induced recruitment domain, the protein tyrosine phosphatases and dual-specificity phosphatases domain and the suppressor of variegation 3-9, enhancer-of-zeste, and trithorax interaction domain. This protein dephosphorylates the target substrates phosphatidylinositol 3-phosphate and inositol 1,3-bisphosphate. A pseudogene of this gene is found on chromosome 5. [provided by RefSeq, Mar 2009]","start":17298030,"end":17413528,"strand":-1,"description":"myotubularin related protein 7 [Source:HGNC Symbol;Acc:HGNC:7454]"}, {"versioned_ensembl_gene_id":"ENSG00000250753.2","gene_symbol":"AC119751.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49579833,"end":49580189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141665.11","gene_symbol":"FBXO15","gene_name":"F-box protein 15 [Source:HGNC Symbol;Acc:HGNC:13617]","synonyms":"MGC39671,FBX15","biotype":"protein_coding","ncbi_id":"201456","summary":"Members of the F-box protein family, such as FBXO15, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":74073353,"end":74147865,"strand":-1,"description":"F-box protein 15 [Source:HGNC Symbol;Acc:HGNC:13617]"}, {"versioned_ensembl_gene_id":"ENSG00000228065.10","gene_symbol":"LINC01515","gene_name":"long intergenic non-protein coding RNA 1515 [Source:HGNC Symbol;Acc:HGNC:51210]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928913","summary":null,"start":65570338,"end":65768835,"strand":1,"description":"long intergenic non-protein coding RNA 1515 [Source:HGNC Symbol;Acc:HGNC:51210]"}, {"versioned_ensembl_gene_id":"ENSG00000203747.10","gene_symbol":"FCGR3A","gene_name":"Fc fragment of IgG receptor IIIa [Source:HGNC Symbol;Acc:HGNC:3619]","synonyms":"FCGR3,FCG3,CD16a,CD16","biotype":"protein_coding","ncbi_id":"2214","summary":"This gene encodes a receptor for the Fc portion of immunoglobulin G, and it is involved in the removal of antigen-antibody complexes from the circulation, as well as other responses, including antibody dependent cellular mediated cytotoxicity and antibody dependent enhancement of virus infections. This gene (FCGR3A) is highly similar to another nearby gene (FCGR3B) located on chromosome 1. The receptor encoded by this gene is expressed on natural killer (NK) cells as an integral membrane glycoprotein anchored through a transmembrane peptide, whereas FCGR3B is expressed on polymorphonuclear neutrophils (PMN) where the receptor is anchored through a phosphatidylinositol (PI) linkage. Mutations in this gene are associated with immunodeficiency 20, and have been linked to susceptibility to recurrent viral infections, susceptibility to systemic lupus erythematosus, and alloimmune neonatal neutropenia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2020]","start":161541759,"end":161550737,"strand":-1,"description":"Fc fragment of IgG receptor IIIa [Source:HGNC Symbol;Acc:HGNC:3619]"}, {"versioned_ensembl_gene_id":"ENSG00000173145.11","gene_symbol":"NOC3L","gene_name":"NOC3 like DNA replication regulator [Source:HGNC Symbol;Acc:HGNC:24034]","synonyms":"FLJ12820,FAD24,C10orf117,AD24","biotype":"protein_coding","ncbi_id":"64318","summary":null,"start":94333226,"end":94362959,"strand":-1,"description":"NOC3 like DNA replication regulator [Source:HGNC Symbol;Acc:HGNC:24034]"}, {"versioned_ensembl_gene_id":"ENSG00000270451.1","gene_symbol":"IGHD4OR15-4B","gene_name":"immunoglobulin heavy diversity 4/OR15-4B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5507]","synonyms":"IGHD4OR154B,IGHD4/OR15-4B","biotype":"IG_D_gene","ncbi_id":"28328","summary":null,"start":21011451,"end":21011469,"strand":-1,"description":"immunoglobulin heavy diversity 4/OR15-4B (non-functional) [Source:HGNC Symbol;Acc:HGNC:5507]"}, {"versioned_ensembl_gene_id":"ENSG00000138430.15","gene_symbol":"OLA1","gene_name":"Obg like ATPase 1 [Source:HGNC Symbol;Acc:HGNC:28833]","synonyms":"PTD004,GTPBP9","biotype":"protein_coding","ncbi_id":"29789","summary":"This gene encodes a member of the GTPase protein family. The encoded protein interacts with breast cancer-associated gene 1 (BRCA1) and BRCA1-associated RING domain protein (BARD1), and is involved in centrosome regulation. Overexpression of this gene has been observed in multiple types of cancer and may be associated with poor survival. Pseudogenes of this gene have been defined on chromosomes 17 and 22. [provided by RefSeq, Jun 2016]","start":174072447,"end":174248698,"strand":-1,"description":"Obg like ATPase 1 [Source:HGNC Symbol;Acc:HGNC:28833]"}, {"versioned_ensembl_gene_id":"ENSG00000231031.6","gene_symbol":"LINC01804","gene_name":"long intergenic non-protein coding RNA 1804 [Source:HGNC Symbol;Acc:HGNC:52596]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926966","summary":null,"start":15690782,"end":15744339,"strand":1,"description":"long intergenic non-protein coding RNA 1804 [Source:HGNC Symbol;Acc:HGNC:52596]"}, {"versioned_ensembl_gene_id":"ENSG00000275740.1","gene_symbol":"AC091959.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":146203550,"end":146339251,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247627.2","gene_symbol":"MTND4P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42199]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100293090","summary":null,"start":134926660,"end":134928036,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42199]"}, {"versioned_ensembl_gene_id":"ENSG00000160867.14","gene_symbol":"FGFR4","gene_name":"fibroblast growth factor receptor 4 [Source:HGNC Symbol;Acc:HGNC:3691]","synonyms":"JTK2,CD334","biotype":"protein_coding","ncbi_id":"2264","summary":"The protein encoded by this gene is a tyrosine kinase and cell surface receptor for fibroblast growth factors. The encoded protein is involved in the regulation of several pathways, including cell proliferation, cell differentiation, cell migration, lipid metabolism, bile acid biosynthesis, vitamin D metabolism, glucose uptake, and phosphate homeostasis. This protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment, and a cytoplasmic tyrosine kinase domain. The extracellular portion interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. [provided by RefSeq, Aug 2017]","start":177086886,"end":177098144,"strand":1,"description":"fibroblast growth factor receptor 4 [Source:HGNC Symbol;Acc:HGNC:3691]"}, {"versioned_ensembl_gene_id":"ENSG00000236177.9","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33205017,"end":33221223,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000267940.1","gene_symbol":"AC022762.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6201901,"end":6203253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154174.7","gene_symbol":"TOMM70","gene_name":"translocase of outer mitochondrial membrane 70 [Source:HGNC Symbol;Acc:HGNC:11985]","synonyms":"TOMM70A,Tom70,KIAA0719","biotype":"protein_coding","ncbi_id":"9868","summary":"This gene encodes an import receptor of the outer mitochondrial membrane that is part of the translocase of the outer membrane complex. This protein is involved in the import of mitochondrial precursor proteins. [provided by RefSeq, Oct 2011]","start":100363431,"end":100401398,"strand":-1,"description":"translocase of outer mitochondrial membrane 70 [Source:HGNC Symbol;Acc:HGNC:11985]"}, {"versioned_ensembl_gene_id":"ENSG00000198868.3","gene_symbol":"MTND4LP30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42264]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075244","summary":null,"start":134928030,"end":134928326,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42264]"}, {"versioned_ensembl_gene_id":"ENSG00000270962.1","gene_symbol":"AC239800.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143784376,"end":143784671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223779.5","gene_symbol":"AC239800.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143745249,"end":143757452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282706.1","gene_symbol":"LINC01043","gene_name":"long intergenic non-protein coding RNA 1043 [Source:HGNC Symbol;Acc:HGNC:49031]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928752","summary":null,"start":112297337,"end":112305608,"strand":1,"description":"long intergenic non-protein coding RNA 1043 [Source:HGNC Symbol;Acc:HGNC:49031]"}, {"versioned_ensembl_gene_id":"ENSG00000183035.12","gene_symbol":"CYLC1","gene_name":"cylicin 1 [Source:HGNC Symbol;Acc:HGNC:2582]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1538","summary":"This gene encodes a sperm head cytoskeletal protein. The encoded protein is associated with the calyx of spermatozoa and spermatids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":83861126,"end":83886699,"strand":1,"description":"cylicin 1 [Source:HGNC Symbol;Acc:HGNC:2582]"}, {"versioned_ensembl_gene_id":"ENSG00000213857.3","gene_symbol":"AL080243.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41074180,"end":41075239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135480.15","gene_symbol":"KRT7","gene_name":"keratin 7 [Source:HGNC Symbol;Acc:HGNC:6445]","synonyms":"SCL,K7,K2C7,CK7","biotype":"protein_coding","ncbi_id":"3855","summary":"The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the simple epithelia lining the cavities of the internal organs and in the gland ducts and blood vessels. The genes encoding the type II cytokeratins are clustered in a region of chromosome 12q12-q13. Alternative splicing may result in several transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":52232520,"end":52252186,"strand":1,"description":"keratin 7 [Source:HGNC Symbol;Acc:HGNC:6445]"}, {"versioned_ensembl_gene_id":"ENSG00000088986.10","gene_symbol":"DYNLL1","gene_name":"dynein light chain LC8-type 1 [Source:HGNC Symbol;Acc:HGNC:15476]","synonyms":"hdlc1,DNCL1,DLC8,DLC1,PIN,LC8","biotype":"protein_coding","ncbi_id":"8655","summary":"Cytoplasmic dyneins are large enzyme complexes with a molecular mass of about 1,200 kD. They contain two force-producing heads formed primarily from dynein heavy chains, and stalks linking the heads to a basal domain, which contains a varying number of accessory intermediate chains. The complex is involved in intracellular transport and motility. The protein described in this record is a light chain and exists as part of this complex but also physically interacts with and inhibits the activity of neuronal nitric oxide synthase. Binding of this protein destabilizes the neuronal nitric oxide synthase dimer, a conformation necessary for activity, and it may regulate numerous biologic processes through its effects on nitric oxide synthase activity. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":120469850,"end":120498493,"strand":1,"description":"dynein light chain LC8-type 1 [Source:HGNC Symbol;Acc:HGNC:15476]"}, {"versioned_ensembl_gene_id":"ENSG00000249620.1","gene_symbol":"AC106774.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17511833,"end":17512238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211694.2","gene_symbol":"TRGV10","gene_name":"T-cell receptor gamma variable 10 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12285]","synonyms":"V3P,TCRGV10","biotype":"TR_V_gene","ncbi_id":"6984","summary":null,"start":38299811,"end":38300322,"strand":-1,"description":"T-cell receptor gamma variable 10 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12285]"}, {"versioned_ensembl_gene_id":"ENSG00000211698.2","gene_symbol":"TRGV4","gene_name":"T-cell receptor gamma variable 4 [Source:HGNC Symbol;Acc:HGNC:12289]","synonyms":"V1S4,TCRGV4","biotype":"TR_V_gene","ncbi_id":"6977","summary":null,"start":38353715,"end":38354517,"strand":-1,"description":"T-cell receptor gamma variable 4 [Source:HGNC Symbol;Acc:HGNC:12289]"}, {"versioned_ensembl_gene_id":"ENSG00000211699.2","gene_symbol":"TRGV3","gene_name":"T-cell receptor gamma variable 3 [Source:HGNC Symbol;Acc:HGNC:12288]","synonyms":"V1S3,TCRGV3","biotype":"TR_V_gene","ncbi_id":"6976","summary":null,"start":38358512,"end":38359162,"strand":-1,"description":"T-cell receptor gamma variable 3 [Source:HGNC Symbol;Acc:HGNC:12288]"}, {"versioned_ensembl_gene_id":"ENSG00000250667.1","gene_symbol":"AC106774.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17495658,"end":17495826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233744.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32588193,"end":32589041,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000244113.1","gene_symbol":"AC079193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17150301,"end":17150888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224875.2","gene_symbol":"AC083949.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42143238,"end":42170301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130052.13","gene_symbol":"STARD8","gene_name":"StAR related lipid transfer domain containing 8 [Source:HGNC Symbol;Acc:HGNC:19161]","synonyms":"KIAA0189,ARHGAP38","biotype":"protein_coding","ncbi_id":"9754","summary":"This gene encodes a member of a subfamily of Rho GTPase activating proteins that contain a steroidogenic acute regulatory protein related lipid transfer domain. The encoded protein localizes to focal adhesions and may be involved in regulating cell morphology. This protein may also function as a tumor suppressor. [provided by RefSeq, Mar 2010]","start":68647666,"end":68725842,"strand":1,"description":"StAR related lipid transfer domain containing 8 [Source:HGNC Symbol;Acc:HGNC:19161]"}, {"versioned_ensembl_gene_id":"ENSG00000255260.1","gene_symbol":"KC877392.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11243188,"end":11243715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278158.1","gene_symbol":"AP001059.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44241847,"end":44242081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234215.2","gene_symbol":"AC006012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69595958,"end":69597448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160298.17","gene_symbol":"C21orf58","gene_name":"chromosome 21 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:1300]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54058","summary":null,"start":46300181,"end":46323875,"strand":-1,"description":"chromosome 21 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:1300]"}, {"versioned_ensembl_gene_id":"ENSG00000256500.5","gene_symbol":"AL139300.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":103562962,"end":103685924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269910.1","gene_symbol":"AL049840.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103694516,"end":103695050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186526.12","gene_symbol":"CYP4F8","gene_name":"cytochrome P450 family 4 subfamily F member 8 [Source:HGNC Symbol;Acc:HGNC:2648]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11283","summary":"This gene, CYP4F8, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and functions as a 19-hydroxylase of prostaglandins in seminal vesicles. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F3, is approximately 18 kb away. [provided by RefSeq, Jul 2008]","start":15615218,"end":15630638,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 8 [Source:HGNC Symbol;Acc:HGNC:2648]"}, {"versioned_ensembl_gene_id":"ENSG00000270858.1","gene_symbol":"VDAC1P5","gene_name":"voltage dependent anion channel 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:12676]","synonyms":"VDAC5P,VDAC3","biotype":"processed_pseudogene","ncbi_id":"10187","summary":null,"start":54802746,"end":54803589,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:12676]"}, {"versioned_ensembl_gene_id":"ENSG00000264364.2","gene_symbol":"DYNLL2","gene_name":"dynein light chain LC8-type 2 [Source:HGNC Symbol;Acc:HGNC:24596]","synonyms":"RSPH22,MGC17810,DNCL1B,Dlc2","biotype":"protein_coding","ncbi_id":"140735","summary":null,"start":58083415,"end":58095536,"strand":1,"description":"dynein light chain LC8-type 2 [Source:HGNC Symbol;Acc:HGNC:24596]"}, {"versioned_ensembl_gene_id":"ENSG00000284676.1","gene_symbol":"AL645944.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29755175,"end":29790597,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235431.1","gene_symbol":"AC004936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9961024,"end":9981817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235054.3","gene_symbol":"LINC01777","gene_name":"long intergenic non-protein coding RNA 1777 [Source:HGNC Symbol;Acc:HGNC:52567]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284661","summary":null,"start":4412027,"end":4424689,"strand":1,"description":"long intergenic non-protein coding RNA 1777 [Source:HGNC Symbol;Acc:HGNC:52567]"}, {"versioned_ensembl_gene_id":"ENSG00000135924.15","gene_symbol":"DNAJB2","gene_name":"DnaJ heat shock protein family (Hsp40) member B2 [Source:HGNC Symbol;Acc:HGNC:5228]","synonyms":"HSPF3,HSJ1,CMT2T","biotype":"protein_coding","ncbi_id":"3300","summary":"This gene is almost exclusively expressed in the brain, mainly in the neuronal layers. It encodes a protein that shows sequence similarity to bacterial DnaJ protein and the yeast homologs. In bacteria, this protein is implicated in protein folding and protein complex dissociation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2011]","start":219279267,"end":219286900,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B2 [Source:HGNC Symbol;Acc:HGNC:5228]"}, {"versioned_ensembl_gene_id":"ENSG00000124788.17","gene_symbol":"ATXN1","gene_name":"ataxin 1 [Source:HGNC Symbol;Acc:HGNC:10548]","synonyms":"SCA1,D6S504E,ATX1","biotype":"protein_coding","ncbi_id":"6310","summary":"The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains 40-83 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). Alternative splicing results in multiple transcript variants, with one variant encoding multiple distinct proteins, ATXN1 and Alt-ATXN1, due to the use of overlapping alternate reading frames. [provided by RefSeq, Nov 2017]","start":16299112,"end":16761491,"strand":-1,"description":"ataxin 1 [Source:HGNC Symbol;Acc:HGNC:10548]"}, {"versioned_ensembl_gene_id":"ENSG00000236895.10","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFB2,P52,TFIIH","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30898049,"end":30903971,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000118596.11","gene_symbol":"SLC16A7","gene_name":"solute carrier family 16 member 7 [Source:HGNC Symbol;Acc:HGNC:10928]","synonyms":"MCT2","biotype":"protein_coding","ncbi_id":"9194","summary":"This gene is a member of the monocarboxylate transporter family. Members in this family transport metabolites, such as lactate, pyruvate, and ketone bodies. The protein encoded by this gene catalyzes the proton-linked transport of monocarboxylates and has the highest affinity for pyruvate. This protein has been reported to be more highly expressed in prostate and colorectal cancer specimens when compared to control specimens. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":59596067,"end":59789855,"strand":1,"description":"solute carrier family 16 member 7 [Source:HGNC Symbol;Acc:HGNC:10928]"}, {"versioned_ensembl_gene_id":"ENSG00000227908.3","gene_symbol":"FLJ31104","gene_name":"uncharacterized LOC441072 [Source:NCBI gene;Acc:441072]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"441072","summary":null,"start":55995167,"end":56003649,"strand":1,"description":"uncharacterized LOC441072 [Source:NCBI gene;Acc:441072]"}, {"versioned_ensembl_gene_id":"ENSG00000261333.2","gene_symbol":"CD24P2","gene_name":"CD24 molecule pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1647]","synonyms":"CD24L2","biotype":"processed_pseudogene","ncbi_id":"936","summary":null,"start":56071421,"end":56071639,"strand":1,"description":"CD24 molecule pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1647]"}, {"versioned_ensembl_gene_id":"ENSG00000246548.3","gene_symbol":"LINC02288","gene_name":"long intergenic non-protein coding RNA 2288 [Source:HGNC Symbol;Acc:HGNC:27505]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283575","summary":null,"start":77041064,"end":77069503,"strand":1,"description":"long intergenic non-protein coding RNA 2288 [Source:HGNC Symbol;Acc:HGNC:27505]"}, {"versioned_ensembl_gene_id":"ENSG00000261573.1","gene_symbol":"AL157402.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":198657553,"end":198667061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279076.1","gene_symbol":"AL136140.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44551577,"end":44553281,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234756.1","gene_symbol":"AC024597.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62289521,"end":62304033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232256.1","gene_symbol":"DDX39B-AS1","gene_name":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478957","summary":null,"start":31529753,"end":31530587,"strand":1,"description":"DDX39B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39771]"}, {"versioned_ensembl_gene_id":"ENSG00000224523.1","gene_symbol":"AL445213.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":81408938,"end":81427276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254113.1","gene_symbol":"AC090193.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123563070,"end":123568762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075043.18","gene_symbol":"KCNQ2","gene_name":"potassium voltage-gated channel subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:6296]","synonyms":"Kv7.2,KCNA11,HNSPC,ENB1,EBN1,EBN,BFNC","biotype":"protein_coding","ncbi_id":"3785","summary":"The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63400210,"end":63472677,"strand":-1,"description":"potassium voltage-gated channel subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:6296]"}, {"versioned_ensembl_gene_id":"ENSG00000228765.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30110194,"end":30111484,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000173848.18","gene_symbol":"NET1","gene_name":"neuroepithelial cell transforming 1 [Source:HGNC Symbol;Acc:HGNC:14592]","synonyms":"NET1A,ARHGEF8","biotype":"protein_coding","ncbi_id":"10276","summary":"This gene is part of the family of Rho guanine nucleotide exchange factors. Members of this family activate Rho proteins by catalyzing the exchange of GDP for GTP. The protein encoded by this gene interacts with RhoA within the cell nucleus and may play a role in repairing DNA damage after ionizing radiation. Pseudogenes of this gene are located on the long arms of chromosomes 1, 7 and 18. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":5412551,"end":5458463,"strand":1,"description":"neuroepithelial cell transforming 1 [Source:HGNC Symbol;Acc:HGNC:14592]"}, {"versioned_ensembl_gene_id":"ENSG00000253188.1","gene_symbol":"TRBV6-7","gene_name":"T-cell receptor beta variable 6-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12232]","synonyms":"TCRBV13S8P,TRBV67,TCRBV6S7","biotype":"TR_V_gene","ncbi_id":"28600","summary":null,"start":142487863,"end":142488295,"strand":1,"description":"T-cell receptor beta variable 6-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12232]"}, {"versioned_ensembl_gene_id":"ENSG00000262222.1","gene_symbol":"AC133065.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10940719,"end":10943021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198169.8","gene_symbol":"ZNF251","gene_name":"zinc finger protein 251 [Source:HGNC Symbol;Acc:HGNC:13045]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90987","summary":null,"start":144720907,"end":144756417,"strand":-1,"description":"zinc finger protein 251 [Source:HGNC Symbol;Acc:HGNC:13045]"}, {"versioned_ensembl_gene_id":"ENSG00000244390.2","gene_symbol":"AC068305.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59020169,"end":59020894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253951.1","gene_symbol":"AC087360.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16275681,"end":16276296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227416.2","gene_symbol":"AL929472.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37782457,"end":37782885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232136.2","gene_symbol":"DUXAP7","gene_name":"double homeobox A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:32186]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503636","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":18642782,"end":18643634,"strand":-1,"description":"double homeobox A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:32186]"}, {"versioned_ensembl_gene_id":"ENSG00000228067.1","gene_symbol":"LINC01740","gene_name":"long intergenic non-protein coding RNA 1740 [Source:HGNC Symbol;Acc:HGNC:52528]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929565","summary":null,"start":212545694,"end":212556065,"strand":1,"description":"long intergenic non-protein coding RNA 1740 [Source:HGNC Symbol;Acc:HGNC:52528]"}, {"versioned_ensembl_gene_id":"ENSG00000213029.3","gene_symbol":"SPHAR","gene_name":"S-phase response (cyclin related) [Source:HGNC Symbol;Acc:HGNC:16957]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10638","summary":null,"start":229304857,"end":229305504,"strand":1,"description":"S-phase response (cyclin related) [Source:HGNC Symbol;Acc:HGNC:16957]"}, {"versioned_ensembl_gene_id":"ENSG00000245526.10","gene_symbol":"LINC00461","gene_name":"long intergenic non-protein coding RNA 461 [Source:HGNC Symbol;Acc:HGNC:42810]","synonyms":"Visc-2,Visc-1b,Visc-1a,LOC645323,EyeLinc1","biotype":"lincRNA","ncbi_id":"645323","summary":"This is an evolutionarily conserved gene that produces alternatively spliced long non-coding RNAs that may be expressed predominantly in the brain and visual cortex. These transcripts may be involved in tumorigenesis, as depletion by siRNA suppressed glioma cell division. Transcripts may also bind to and regulate the activity of miR-411-5p and argonaut 2, thereby altering the expression of genes involved in tumor growth. [provided by RefSeq, Nov 2017]","start":88507546,"end":88691041,"strand":-1,"description":"long intergenic non-protein coding RNA 461 [Source:HGNC Symbol;Acc:HGNC:42810]"}, {"versioned_ensembl_gene_id":"ENSG00000146918.19","gene_symbol":"NCAPG2","gene_name":"non-SMC condensin II complex subunit G2 [Source:HGNC Symbol;Acc:HGNC:21904]","synonyms":"MTB,LUZP5,hCAP-G2,FLJ20311,CAP-G2","biotype":"protein_coding","ncbi_id":"54892","summary":"This gene encodes a protein that belongs to the Condensin2nSMC family of proteins. The encoded protein is a regulatory subunit of the condensin II complex which, along with the condensin I complex, plays a role in chromosome assembly and segregation during mitosis. A similar protein in mouse is required for early development of the embryo. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":158631311,"end":158704829,"strand":-1,"description":"non-SMC condensin II complex subunit G2 [Source:HGNC Symbol;Acc:HGNC:21904]"}, {"versioned_ensembl_gene_id":"ENSG00000270708.1","gene_symbol":"KF455155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220220291,"end":220220593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273855.1","gene_symbol":"AC020658.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40285468,"end":40285909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249330.1","gene_symbol":"AC095060.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46390255,"end":46433188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166086.12","gene_symbol":"JAM3","gene_name":"junctional adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:15532]","synonyms":"JAMC,JAM-C","biotype":"protein_coding","ncbi_id":"83700","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. The protein encoded by this immunoglobulin superfamily gene member is localized in the tight junctions between high endothelial cells. Unlike other proteins in this family, the this protein is unable to adhere to leukocyte cell lines and only forms weak homotypic interactions. The encoded protein is a member of the junctional adhesion molecule protein family and acts as a receptor for another member of this family. A mutation in an intron of this gene is associated with hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011]","start":134068925,"end":134152001,"strand":1,"description":"junctional adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:15532]"}, {"versioned_ensembl_gene_id":"ENSG00000187243.16","gene_symbol":"MAGED4B","gene_name":"MAGE family member D4B [Source:HGNC Symbol;Acc:HGNC:22880]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81557","summary":"This gene is a member of the MAGED gene family. It is expressed only in brain and ovary, and some transcript variants of this gene are specifically expressed in glioma cells. This gene is clustered with other MAGED genes on chromosome Xp11. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]","start":52061827,"end":52069248,"strand":-1,"description":"MAGE family member D4B [Source:HGNC Symbol;Acc:HGNC:22880]"}, {"versioned_ensembl_gene_id":"ENSG00000269786.1","gene_symbol":"AC044792.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56922018,"end":56922213,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177800.2","gene_symbol":"TMEM78","gene_name":"transmembrane protein 78 [Source:HGNC Symbol;Acc:HGNC:32307]","synonyms":"FLJ40168","biotype":"protein_coding","ncbi_id":"677790","summary":null,"start":229249636,"end":229251810,"strand":1,"description":"transmembrane protein 78 [Source:HGNC Symbol;Acc:HGNC:32307]"}, {"versioned_ensembl_gene_id":"ENSG00000232124.1","gene_symbol":"AP001057.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44201290,"end":44202696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233920.1","gene_symbol":"AL162595.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":229223461,"end":229227562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229840.2","gene_symbol":"ISCA1P2","gene_name":"iron-sulfur cluster assembly 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288517","summary":null,"start":229042171,"end":229042591,"strand":1,"description":"iron-sulfur cluster assembly 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38023]"}, {"versioned_ensembl_gene_id":"ENSG00000253858.1","gene_symbol":"AC008619.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170483806,"end":170486407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225331.1","gene_symbol":"LINC01678","gene_name":"long intergenic non-protein coding RNA 1678 [Source:HGNC Symbol;Acc:HGNC:52466]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377138","summary":null,"start":44158740,"end":44160076,"strand":-1,"description":"long intergenic non-protein coding RNA 1678 [Source:HGNC Symbol;Acc:HGNC:52466]"}, {"versioned_ensembl_gene_id":"ENSG00000267354.1","gene_symbol":"AC091151.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45507202,"end":45550183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225165.3","gene_symbol":"AC090071.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95440044,"end":95440687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232802.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33081698,"end":33081901,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000107890.16","gene_symbol":"ANKRD26","gene_name":"ankyrin repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:29186]","synonyms":"THC2,KIAA1074","biotype":"protein_coding","ncbi_id":"22852","summary":"This gene encodes a protein containing N-terminal ankyrin repeats which function in protein-protein interactions. Mutations in this gene are associated with autosomal dominant thrombocytopenia-2. Pseudogenes of this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":26991914,"end":27100498,"strand":-1,"description":"ankyrin repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:29186]"}, {"versioned_ensembl_gene_id":"ENSG00000248583.1","gene_symbol":"AC119751.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49486926,"end":49489554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273041.1","gene_symbol":"ATF4P2","gene_name":"activating transcription factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340600","summary":null,"start":154580926,"end":154581998,"strand":1,"description":"activating transcription factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34025]"}, {"versioned_ensembl_gene_id":"ENSG00000157954.14","gene_symbol":"WIPI2","gene_name":"WD repeat domain, phosphoinositide interacting 2 [Source:HGNC Symbol;Acc:HGNC:32225]","synonyms":"DKFZp686P02188,DKFZP434J154,CGI-50,ATG21,ATG18B,FLJ42984,FLJ14217,FLJ12979","biotype":"protein_coding","ncbi_id":"26100","summary":"WD40 repeat proteins are key components of many essential biologic functions. They regulate the assembly of multiprotein complexes by presenting a beta-propeller platform for simultaneous and reversible protein-protein interactions. Members of the WIPI subfamily of WD40 repeat proteins, such as WIPI2, have a 7-bladed propeller structure and contain a conserved motif for interaction with phospholipids (Proikas-Cezanne et al., 2004 [PubMed 15602573]).[supplied by OMIM, Mar 2008]","start":5190188,"end":5233826,"strand":1,"description":"WD repeat domain, phosphoinositide interacting 2 [Source:HGNC Symbol;Acc:HGNC:32225]"}, {"versioned_ensembl_gene_id":"ENSG00000237961.4","gene_symbol":"AC118282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49238032,"end":49245419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087494.15","gene_symbol":"PTHLH","gene_name":"parathyroid hormone like hormone [Source:HGNC Symbol;Acc:HGNC:9607]","synonyms":"PTHRP,PTHR,PLP,HHM","biotype":"protein_coding","ncbi_id":"5744","summary":"The protein encoded by this gene is a member of the parathyroid hormone family. This hormone, via its receptor, PTHR1, regulates endochondral bone development and epithelial-mesenchymal interactions during the formation of the mammary glands and teeth. It is responsible for most cases of humoral hypercalcemia of malignancy, and mutations in this gene are associated with brachydactyly type E2 (BDE2). Alternatively spliced transcript variants have been found for this gene. There is also evidence for alternative translation initiation from non-AUG (CUG and GUG) start sites, downstream of the initiator AUG codon, resulting in nuclear forms of this hormone. [provided by RefSeq, Nov 2013]","start":27958084,"end":27972705,"strand":-1,"description":"parathyroid hormone like hormone [Source:HGNC Symbol;Acc:HGNC:9607]"}, {"versioned_ensembl_gene_id":"ENSG00000218749.1","gene_symbol":"AL033519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35607628,"end":35607934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258603.3","gene_symbol":"AC005225.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73616700,"end":73633941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258972.1","gene_symbol":"AC005225.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73631475,"end":73632019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256007.1","gene_symbol":"ARAP1-AS1","gene_name":"ARAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39993]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874075","summary":null,"start":72685075,"end":72693808,"strand":1,"description":"ARAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39993]"}, {"versioned_ensembl_gene_id":"ENSG00000255062.1","gene_symbol":"AP001318.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126294298,"end":126304318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280868.1","gene_symbol":"LINC00242","gene_name":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]","synonyms":"dJ266L20.5,C6orf122,NCRNA00242,FLJ31451","biotype":"lincRNA","ncbi_id":"401288","summary":null,"start":169788790,"end":169798825,"strand":-1,"description":"long intergenic non-protein coding RNA 242 [Source:HGNC Symbol;Acc:HGNC:21249]"}, {"versioned_ensembl_gene_id":"ENSG00000214919.3","gene_symbol":"AC104472.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":155742142,"end":155743726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253691.2","gene_symbol":"IGKV2OR22-4","gene_name":"immunoglobulin kappa variable 2/OR22-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5813]","synonyms":"IGKVP6,IGKV2/OR22-4","biotype":"IG_V_pseudogene","ncbi_id":"28847","summary":null,"start":16914235,"end":16914981,"strand":-1,"description":"immunoglobulin kappa variable 2/OR22-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5813]"}, {"versioned_ensembl_gene_id":"ENSG00000166118.7","gene_symbol":"SPATA19","gene_name":"spermatogenesis associated 19 [Source:HGNC Symbol;Acc:HGNC:30614]","synonyms":"spergen1,SPAS1,FLJ25851,CT132","biotype":"protein_coding","ncbi_id":"219938","summary":null,"start":133840631,"end":133845538,"strand":-1,"description":"spermatogenesis associated 19 [Source:HGNC Symbol;Acc:HGNC:30614]"}, {"versioned_ensembl_gene_id":"ENSG00000280708.1","gene_symbol":"AC006359.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144567601,"end":144568743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141469.16","gene_symbol":"SLC14A1","gene_name":"solute carrier family 14 member 1 (Kidd blood group) [Source:HGNC Symbol;Acc:HGNC:10918]","synonyms":"RACH2,RACH1,JK,HsT1341","biotype":"protein_coding","ncbi_id":"6563","summary":"The protein encoded by this gene is a membrane transporter that mediates urea transport in erythrocytes. This gene forms the basis for the Kidd blood group system. [provided by RefSeq, Mar 2009]","start":45724127,"end":45752520,"strand":1,"description":"solute carrier family 14 member 1 (Kidd blood group) [Source:HGNC Symbol;Acc:HGNC:10918]"}, {"versioned_ensembl_gene_id":"ENSG00000163001.11","gene_symbol":"CFAP36","gene_name":"cilia and flagella associated protein 36 [Source:HGNC Symbol;Acc:HGNC:30540]","synonyms":"MGC15407,CCDC104,BARTL1","biotype":"protein_coding","ncbi_id":"112942","summary":null,"start":55519604,"end":55545879,"strand":1,"description":"cilia and flagella associated protein 36 [Source:HGNC Symbol;Acc:HGNC:30540]"}, {"versioned_ensembl_gene_id":"ENSG00000144824.20","gene_symbol":"PHLDB2","gene_name":"pleckstrin homology like domain family B member 2 [Source:HGNC Symbol;Acc:HGNC:29573]","synonyms":"LL5beta,LL5b,FLJ21791","biotype":"protein_coding","ncbi_id":"90102","summary":null,"start":111732497,"end":111976517,"strand":1,"description":"pleckstrin homology like domain family B member 2 [Source:HGNC Symbol;Acc:HGNC:29573]"}, {"versioned_ensembl_gene_id":"ENSG00000106537.7","gene_symbol":"TSPAN13","gene_name":"tetraspanin 13 [Source:HGNC Symbol;Acc:HGNC:21643]","synonyms":"TM4SF13,NET-6","biotype":"protein_coding","ncbi_id":"27075","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. [provided by RefSeq, Jul 2008]","start":16753535,"end":16784536,"strand":1,"description":"tetraspanin 13 [Source:HGNC Symbol;Acc:HGNC:21643]"}, {"versioned_ensembl_gene_id":"ENSG00000281948.1","gene_symbol":"CES1P1","gene_name":"carboxylesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18546]","synonyms":"PCE-3,CESR,CES4,CES1A3","biotype":"unprocessed_pseudogene","ncbi_id":"51716","summary":"This gene is a member of the carboxylesterase (CES) gene family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene does not encode a protein and the sequence is similar to the CES1 gene, so represents a pseudogene of the CES1 gene. [provided by RefSeq, Jun 2010]","start":55773402,"end":55790834,"strand":1,"description":"carboxylesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18546]"}, {"versioned_ensembl_gene_id":"ENSG00000267215.1","gene_symbol":"AC040963.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59081924,"end":59084981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198755.10","gene_symbol":"RPL10A","gene_name":"ribosomal protein L10a [Source:HGNC Symbol;Acc:HGNC:10299]","synonyms":"NEDD6,L10A,Csa-19","biotype":"protein_coding","ncbi_id":"4736","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L1P family of ribosomal proteins. It is located in the cytoplasm. The expression of this gene is downregulated in the thymus by cyclosporin-A (CsA), an immunosuppressive drug. Studies in mice have shown that the expression of the ribosomal protein L10a gene is downregulated in neural precursor cells during development. This gene previously was referred to as NEDD6 (neural precursor cell expressed, developmentally downregulated 6), but it has been renamed RPL10A (ribosomal protein 10a). As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":35468408,"end":35470785,"strand":1,"description":"ribosomal protein L10a [Source:HGNC Symbol;Acc:HGNC:10299]"}, {"versioned_ensembl_gene_id":"ENSG00000183317.16","gene_symbol":"EPHA10","gene_name":"EPH receptor A10 [Source:HGNC Symbol;Acc:HGNC:19987]","synonyms":"FLJ33655,FLJ16103","biotype":"protein_coding","ncbi_id":"284656","summary":"Ephrin receptors, the largest subfamily of receptor tyrosine kinases (RTKs), and their ephrin ligands are important mediators of cell-cell communication regulating cell attachment, shape, and mobility in neuronal and epithelial cells (Aasheim et al., 2005 [PubMed 15777695]). See MIM 179610 for additional background on Eph receptors and ephrins.[supplied by OMIM, Mar 2008]","start":37713880,"end":37765133,"strand":-1,"description":"EPH receptor A10 [Source:HGNC Symbol;Acc:HGNC:19987]"}, {"versioned_ensembl_gene_id":"ENSG00000226131.1","gene_symbol":"AC073465.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173485865,"end":173486362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137968.16","gene_symbol":"SLC44A5","gene_name":"solute carrier family 44 member 5 [Source:HGNC Symbol;Acc:HGNC:28524]","synonyms":"MGC34032,CTL5","biotype":"protein_coding","ncbi_id":"204962","summary":null,"start":75202131,"end":75611116,"strand":-1,"description":"solute carrier family 44 member 5 [Source:HGNC Symbol;Acc:HGNC:28524]"}, {"versioned_ensembl_gene_id":"ENSG00000276578.1","gene_symbol":"AC004696.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56485923,"end":56494280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236086.4","gene_symbol":"HMGN2P28","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39395]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128372","summary":null,"start":2341450,"end":2341711,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39395]"}, {"versioned_ensembl_gene_id":"ENSG00000267012.1","gene_symbol":"AC011456.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31886704,"end":31908284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256013.1","gene_symbol":"AC027277.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10529440,"end":10532082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152292.16","gene_symbol":"SH2D6","gene_name":"SH2 domain containing 6 [Source:HGNC Symbol;Acc:HGNC:30439]","synonyms":"FLJ35993","biotype":"protein_coding","ncbi_id":"284948","summary":null,"start":85418721,"end":85437029,"strand":1,"description":"SH2 domain containing 6 [Source:HGNC Symbol;Acc:HGNC:30439]"}, {"versioned_ensembl_gene_id":"ENSG00000081189.15","gene_symbol":"MEF2C","gene_name":"myocyte enhancer factor 2C [Source:HGNC Symbol;Acc:HGNC:6996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4208","summary":"This locus encodes a member of the MADS box transcription enhancer factor 2 (MEF2) family of proteins, which play a role in myogenesis. The encoded protein, MEF2 polypeptide C, has both trans-activating and DNA binding activities. This protein may play a role in maintaining the differentiated state of muscle cells. Mutations and deletions at this locus have been associated with severe cognitive disability, stereotypic movements, epilepsy, and cerebral malformation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2010]","start":88717117,"end":88904257,"strand":-1,"description":"myocyte enhancer factor 2C [Source:HGNC Symbol;Acc:HGNC:6996]"}, {"versioned_ensembl_gene_id":"ENSG00000250555.2","gene_symbol":"AC008525.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88692651,"end":88692859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103274.10","gene_symbol":"NUBP1","gene_name":"nucleotide binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8041]","synonyms":"NBP35,NBP1","biotype":"protein_coding","ncbi_id":"4682","summary":"NUBP1 is a member of the NUBP/MRP subfamily of ATP-binding proteins (Nakashima et al., 1999 [PubMed 10486206]).[supplied by OMIM, Mar 2008]","start":10743786,"end":10769351,"strand":1,"description":"nucleotide binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8041]"}, {"versioned_ensembl_gene_id":"ENSG00000279077.1","gene_symbol":"AC023090.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79352458,"end":79354567,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255504.2","gene_symbol":"AP001533.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":101208905,"end":101209450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269891.2","gene_symbol":"ARHGAP19-SLIT1","gene_name":"ARHGAP19-SLIT1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48348]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533184","summary":"This locus represents naturally occurring read-through transcription between the neighboring Rho GTPase activating protein 19 (ARHGAP19) and slit homolog 1 (SLIT1) genes on chromosome 10. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":97153045,"end":97292637,"strand":-1,"description":"ARHGAP19-SLIT1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48348]"}, {"versioned_ensembl_gene_id":"ENSG00000237223.6","gene_symbol":"SULT1C2P1","gene_name":"sulfotransferase family 1C member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33545]","synonyms":"SULT1C1P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"151234","summary":null,"start":108322238,"end":108353799,"strand":1,"description":"sulfotransferase family 1C member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33545]"}, {"versioned_ensembl_gene_id":"ENSG00000260104.1","gene_symbol":"AC068338.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75249232,"end":75249407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282557.1","gene_symbol":"AC093627.17","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79359,"end":82739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215070.4","gene_symbol":"XRCC6P5","gene_name":"X-ray repair cross complementing 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45187]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442459","summary":null,"start":99719364,"end":99721158,"strand":-1,"description":"X-ray repair cross complementing 6 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45187]"}, {"versioned_ensembl_gene_id":"ENSG00000128310.2","gene_symbol":"GALR3","gene_name":"galanin receptor 3 [Source:HGNC Symbol;Acc:HGNC:4134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8484","summary":"The neuropeptide galanin modulates a variety of physiologic processes including cognition/memory, sensory/pain processing, hormone secretion, and feeding behavior. The human galanin receptors are G protein-coupled receptors that functionally couple to their intracellular effector through distinct signaling pathways. GALR3 is found in many tissues and may be expressed as 1.4-, 2.4-, and 5-kb transcripts [provided by RefSeq, Jul 2008]","start":37823382,"end":37825495,"strand":1,"description":"galanin receptor 3 [Source:HGNC Symbol;Acc:HGNC:4134]"}, {"versioned_ensembl_gene_id":"ENSG00000177752.14","gene_symbol":"YIPF7","gene_name":"Yip1 domain family member 7 [Source:HGNC Symbol;Acc:HGNC:26825]","synonyms":"FLJ39576,FinGER9","biotype":"protein_coding","ncbi_id":"285525","summary":null,"start":44622065,"end":44678556,"strand":-1,"description":"Yip1 domain family member 7 [Source:HGNC Symbol;Acc:HGNC:26825]"}, {"versioned_ensembl_gene_id":"ENSG00000270393.1","gene_symbol":"AC000095.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19018043,"end":19018916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260869.1","gene_symbol":"AC002310.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30534227,"end":30558279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253384.1","gene_symbol":"AC124242.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18088569,"end":18089687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169951.9","gene_symbol":"ZNF764","gene_name":"zinc finger protein 764 [Source:HGNC Symbol;Acc:HGNC:28200]","synonyms":"MGC13138","biotype":"protein_coding","ncbi_id":"92595","summary":null,"start":30553764,"end":30558498,"strand":-1,"description":"zinc finger protein 764 [Source:HGNC Symbol;Acc:HGNC:28200]"}, {"versioned_ensembl_gene_id":"ENSG00000278922.1","gene_symbol":"AC002310.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30526918,"end":30528294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180066.9","gene_symbol":"C10orf91","gene_name":"chromosome 10 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:27275]","synonyms":"bA432J24.4","biotype":"lincRNA","ncbi_id":"170393","summary":null,"start":132444327,"end":132449408,"strand":1,"description":"chromosome 10 open reading frame 91 [Source:HGNC Symbol;Acc:HGNC:27275]"}, {"versioned_ensembl_gene_id":"ENSG00000172967.7","gene_symbol":"XKR3","gene_name":"XK related 3 [Source:HGNC Symbol;Acc:HGNC:28778]","synonyms":"XTES,MGC57211","biotype":"protein_coding","ncbi_id":"150165","summary":"XKRX (MIM 300684) and XKR3 are homologs of the Kell blood group precursor XK (MIM 314850), which is a putative membrane transporter and a component of the XK/Kell complex of the Kell blood group system (Calenda et al., 2006 [PubMed 16431037]).[supplied by OMIM, Mar 2008]","start":16783412,"end":16821699,"strand":-1,"description":"XK related 3 [Source:HGNC Symbol;Acc:HGNC:28778]"}, {"versioned_ensembl_gene_id":"ENSG00000253906.1","gene_symbol":"IGKV2D-10","gene_name":"immunoglobulin kappa variable 2D-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5792]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28890","summary":null,"start":90179889,"end":90180587,"strand":1,"description":"immunoglobulin kappa variable 2D-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5792]"}, {"versioned_ensembl_gene_id":"ENSG00000213704.3","gene_symbol":"EEF1A1P15","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3198]","synonyms":"EEF1AL13","biotype":"processed_pseudogene","ncbi_id":"643563","summary":null,"start":98389512,"end":98390919,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:3198]"}, {"versioned_ensembl_gene_id":"ENSG00000224149.1","gene_symbol":"AC099786.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75129974,"end":75132576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105854.12","gene_symbol":"PON2","gene_name":"paraoxonase 2 [Source:HGNC Symbol;Acc:HGNC:9205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5445","summary":"This gene encodes a member of the paraoxonase gene family, which includes three known members located adjacent to each other on the long arm of chromosome 7. The encoded protein is ubiquitously expressed in human tissues, membrane-bound, and may act as a cellular antioxidant, protecting cells from oxidative stress. Hydrolytic activity against acylhomoserine lactones, important bacterial quorum-sensing mediators, suggests the encoded protein may also play a role in defense responses to pathogenic bacteria. Mutations in this gene may be associated with vascular disease and a number of quantitative phenotypes related to diabetes. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":95404863,"end":95435329,"strand":-1,"description":"paraoxonase 2 [Source:HGNC Symbol;Acc:HGNC:9205]"}, {"versioned_ensembl_gene_id":"ENSG00000248117.1","gene_symbol":"MINOS1P4","gene_name":"mitochondrial inner membrane organizing system 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44094]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462957","summary":null,"start":78379197,"end":78379514,"strand":1,"description":"mitochondrial inner membrane organizing system 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44094]"}, {"versioned_ensembl_gene_id":"ENSG00000153060.7","gene_symbol":"TEKT5","gene_name":"tektin 5 [Source:HGNC Symbol;Acc:HGNC:26554]","synonyms":"FLJ32871,CT149","biotype":"protein_coding","ncbi_id":"146279","summary":null,"start":10627501,"end":10694945,"strand":-1,"description":"tektin 5 [Source:HGNC Symbol;Acc:HGNC:26554]"}, {"versioned_ensembl_gene_id":"ENSG00000229474.6","gene_symbol":"PATL2","gene_name":"PAT1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:33630]","synonyms":"Pat1a","biotype":"protein_coding","ncbi_id":"197135","summary":null,"start":44665732,"end":44711316,"strand":-1,"description":"PAT1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:33630]"}, {"versioned_ensembl_gene_id":"ENSG00000233592.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29809446,"end":29809577,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000282294.1","gene_symbol":"IGHVIII-51-1","gene_name":"immunoglobulin heavy variable (III)-51-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5704]","synonyms":"IGHV(III)-51-1","biotype":"IG_V_pseudogene","ncbi_id":"28343","summary":null,"start":106608187,"end":106608488,"strand":-1,"description":"immunoglobulin heavy variable (III)-51-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5704]"}, {"versioned_ensembl_gene_id":"ENSG00000265728.1","gene_symbol":"AP001099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10594590,"end":10604798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273688.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786274,"end":54790272,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000198019.12","gene_symbol":"FCGR1B","gene_name":"Fc fragment of IgG receptor Ib [Source:HGNC Symbol;Acc:HGNC:3614]","synonyms":"CD64b","biotype":"protein_coding","ncbi_id":"2210","summary":"Three distinct, but closely related classes of receptors that bind the Fc portion of IgG have been identified (Fcgamma RI, II and III). The FcgammaRI family consists of three closely related genes termed A, B, and C. This gene likely encodes a non-functional protein that is not detectable at the cell surface and binds ligand with low affinity. [provided by RefSeq, Nov 2019]","start":121087345,"end":121096310,"strand":1,"description":"Fc fragment of IgG receptor Ib [Source:HGNC Symbol;Acc:HGNC:3614]"}, {"versioned_ensembl_gene_id":"ENSG00000271364.1","gene_symbol":"AC015871.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79984151,"end":79985724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233038.5","gene_symbol":"AC011899.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157854529,"end":157866092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250365.6","gene_symbol":"AL139353.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31420286,"end":31452883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258410.1","gene_symbol":"AC087386.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20128745,"end":20147953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124535.15","gene_symbol":"WRNIP1","gene_name":"Werner helicase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20876]","synonyms":"WHIP,FLJ22526,bA420G6.2","biotype":"protein_coding","ncbi_id":"56897","summary":"Werner's syndrome is a rare autosomal recessive disorder characterized by accelerated aging that is caused by defects in the Werner syndrome ATP-dependent helicase gene (WRN). The protein encoded by this gene interacts with the exonuclease-containing N-terminal portion of the Werner protein. This protein has a ubiquitin-binding zinc-finger domain in the N-terminus, an ATPase domain, and two leucine zipper motifs in the C-terminus. It has sequence similarity to replication factor C family proteins and is conserved from E. coli to human. This protein likely accumulates at sites of DNA damage by interacting with polyubiquinated proteins and also binds to DNA polymerase delta and increases the initiation frequency of DNA polymerase delta-mediated DNA synthesis. This protein also interacts with nucleoporins at nuclear pore complexes. Two transcript variants encoding different isoforms have been isolated for this gene. [provided by RefSeq, Jul 2012]","start":2765414,"end":2786952,"strand":1,"description":"Werner helicase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20876]"}, {"versioned_ensembl_gene_id":"ENSG00000231485.1","gene_symbol":"AL357078.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65066627,"end":65067737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267338.1","gene_symbol":"AP000365.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16616170,"end":16617114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267778.1","gene_symbol":"AC004221.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1238179,"end":1239522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267629.3","gene_symbol":"AC138430.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19254748,"end":19273369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256377.5","gene_symbol":"AC009509.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27696388,"end":27710770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273800.1","gene_symbol":"AC119619.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12583415,"end":12583526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267429.1","gene_symbol":"AC006116.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56347081,"end":56348183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254220.1","gene_symbol":"IGKV2D-18","gene_name":"immunoglobulin kappa variable 2D-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5794]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28888","summary":null,"start":90052581,"end":90053372,"strand":1,"description":"immunoglobulin kappa variable 2D-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5794]"}, {"versioned_ensembl_gene_id":"ENSG00000279136.1","gene_symbol":"AL031258.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":769119,"end":769443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156802.12","gene_symbol":"ATAD2","gene_name":"ATPase family, AAA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30123]","synonyms":"MGC5254,MGC29843,DKFZp667N1320,CT137,PRO2000","biotype":"protein_coding","ncbi_id":"29028","summary":"A large family of ATPases has been described, whose key feature is that they share a conserved region of about 220 amino acids that contains an ATP-binding site. The proteins that belong to this family either contain one or two AAA (ATPases Associated with diverse cellular Activities) domains. AAA family proteins often perform chaperone-like functions that assist in the assembly, operation, or disassembly of protein complexes. The protein encoded by this gene contains two AAA domains, as well as a bromodomain. [provided by RefSeq, Jul 2008]","start":123319850,"end":123416350,"strand":-1,"description":"ATPase family, AAA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30123]"}, {"versioned_ensembl_gene_id":"ENSG00000231735.1","gene_symbol":"AC092573.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173297629,"end":173298512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226264.10","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32912565,"end":32931062,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000276126.3","gene_symbol":"GAL3ST2","gene_name":"galactose-3-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:24869]","synonyms":"GP3ST","biotype":"protein_coding","ncbi_id":"64090","summary":"This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the hydroxyl at C-3 of nonreducing beta-galactosyl residues, and it can act on both type 1 and type 2 (Galbeta 1-3/1-4GlcNAc-R) oligosaccharides with similar efficiencies, and on core 1 glycans. This enzyme has been implicated in tumor metastasis processes. This gene is different from the GAL3ST3 gene located on chromosome 11, which has also been referred to as GAL3ST2 and encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 2. [provided by RefSeq, Jul 2008]","start":241799063,"end":241804208,"strand":1,"description":"galactose-3-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:24869]"}, {"versioned_ensembl_gene_id":"ENSG00000152592.13","gene_symbol":"DMP1","gene_name":"dentin matrix acidic phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:2932]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1758","summary":"Dentin matrix acidic phosphoprotein is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein family. This protein, which is critical for proper mineralization of bone and dentin, is present in diverse cells of bone and tooth tissues. The protein contains a large number of acidic domains, multiple phosphorylation sites, a functional arg-gly-asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts it is primarily a nuclear protein that regulates the expression of osteoblast-specific genes. During osteoblast maturation the protein becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in the gene are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. The gene structure is conserved in mammals. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":87650307,"end":87664361,"strand":1,"description":"dentin matrix acidic phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:2932]"}, {"versioned_ensembl_gene_id":"ENSG00000278893.1","gene_symbol":"AC010533.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":64981123,"end":64983227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281956.1","gene_symbol":"IGHVII-44-2","gene_name":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]","synonyms":"IGHV(II)-44-2","biotype":"IG_V_pseudogene","ncbi_id":"28366","summary":null,"start":106518815,"end":106519064,"strand":-1,"description":"immunoglobulin heavy variable (II)-44-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5681]"}, {"versioned_ensembl_gene_id":"ENSG00000254001.5","gene_symbol":"AC084706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78148101,"end":78153913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282180.1","gene_symbol":"IGHV3-42","gene_name":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28427","summary":null,"start":106487939,"end":106488239,"strand":-1,"description":"immunoglobulin heavy variable 3-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5603]"}, {"versioned_ensembl_gene_id":"ENSG00000232351.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32690654,"end":32691504,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000106178.6","gene_symbol":"CCL24","gene_name":"C-C motif chemokine ligand 24 [Source:HGNC Symbol;Acc:HGNC:10623]","synonyms":"SCYA24,MPIF2,MPIF-2,eotaxin-2,Ckb-6","biotype":"protein_coding","ncbi_id":"6369","summary":"This gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity on resting T lymphocytes, a minimal activity on neutrophils, and is negative on monocytes and activated T lymphocytes. This protein also has antimicrobial activity, displaying an antibacterial effect on S. pneumoniae, S. aureus, Non-typeable H. influenzae, and P. aeruginosa. Finally, the protein is a strong suppressor of colony formation by a multipotential hematopoietic progenitor cell line. [provided by RefSeq, Jul 2020]","start":75811665,"end":75823356,"strand":-1,"description":"C-C motif chemokine ligand 24 [Source:HGNC Symbol;Acc:HGNC:10623]"}, {"versioned_ensembl_gene_id":"ENSG00000196071.5","gene_symbol":"OR2L13","gene_name":"olfactory receptor family 2 subfamily L member 13 [Source:HGNC Symbol;Acc:HGNC:19578]","synonyms":"OR2L14","biotype":"protein_coding","ncbi_id":"284521","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248095184,"end":248101103,"strand":1,"description":"olfactory receptor family 2 subfamily L member 13 [Source:HGNC Symbol;Acc:HGNC:19578]"}, {"versioned_ensembl_gene_id":"ENSG00000197272.2","gene_symbol":"IL27","gene_name":"interleukin 27 [Source:HGNC Symbol;Acc:HGNC:19157]","synonyms":"p28,MGC71873,IL30,IL27p28,IL27A,IL-27A,IL-27","biotype":"protein_coding","ncbi_id":"246778","summary":"The protein encoded by this gene is one of the subunits of a heterodimeric cytokine complex. This protein is related to interleukin 12A (IL12A). It interacts with Epstein-Barr virus induced gene 3 (EBI3), a protein similar to interleukin 12B (IL12B), and forms a complex that has been shown to drive rapid expansion of naive but not memory CD4(+) T cells. The complex is also found to synergize strongly with interleukin 12 to trigger interferon gamma (IFNG) production of naive CD4(+) T cells. The biological effects of this cytokine are mediated by the class I cytokine receptor (WSX1/TCRR). [provided by RefSeq, Jul 2008]","start":28499362,"end":28512051,"strand":-1,"description":"interleukin 27 [Source:HGNC Symbol;Acc:HGNC:19157]"}, {"versioned_ensembl_gene_id":"ENSG00000203663.4","gene_symbol":"OR2L2","gene_name":"olfactory receptor family 2 subfamily L member 2 [Source:HGNC Symbol;Acc:HGNC:8266]","synonyms":"OR2L4P,OR2L12,HTPCRH07,HSHTPCRH07","biotype":"protein_coding","ncbi_id":"26246","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248030070,"end":248042305,"strand":1,"description":"olfactory receptor family 2 subfamily L member 2 [Source:HGNC Symbol;Acc:HGNC:8266]"}, {"versioned_ensembl_gene_id":"ENSG00000256684.1","gene_symbol":"AP003781.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96508425,"end":96514748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077943.7","gene_symbol":"ITGA8","gene_name":"integrin subunit alpha 8 [Source:HGNC Symbol;Acc:HGNC:6144]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8516","summary":"Integrins are heterodimeric transmembrane receptor proteins that mediate numerous cellular processes including cell adhesion, cytoskeletal rearrangement, and activation of cell signaling pathways. Integrins are composed of alpha and beta subunits. This gene encodes the alpha 8 subunit of the heterodimeric integrin alpha8beta1 protein. The encoded protein is a single-pass type 1 membrane protein that contains multiple FG-GAP repeats. This repeat is predicted to fold into a beta propeller structure. This gene regulates the recruitment of mesenchymal cells into epithelial structures, mediates cell-cell interactions, and regulates neurite outgrowth of sensory and motor neurons. The integrin alpha8beta1 protein thus plays an important role in wound-healing and organogenesis. Mutations in this gene have been associated with renal hypodysplasia/aplasia-1 (RHDA1) and with several animal models of chronic kidney disease. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2014]","start":15513949,"end":15720125,"strand":-1,"description":"integrin subunit alpha 8 [Source:HGNC Symbol;Acc:HGNC:6144]"}, {"versioned_ensembl_gene_id":"ENSG00000259010.1","gene_symbol":"AL049869.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64600243,"end":64601644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145247.11","gene_symbol":"OCIAD2","gene_name":"OCIA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28685]","synonyms":"MGC45416","biotype":"protein_coding","ncbi_id":"132299","summary":null,"start":48885019,"end":48906937,"strand":-1,"description":"OCIA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28685]"}, {"versioned_ensembl_gene_id":"ENSG00000280485.1","gene_symbol":"AL358154.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93772681,"end":93788605,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228431.1","gene_symbol":"ARL5AP3","gene_name":"ADP ribosylation factor like GTPase 5A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480778","summary":null,"start":68049360,"end":68049745,"strand":-1,"description":"ADP ribosylation factor like GTPase 5A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43935]"}, {"versioned_ensembl_gene_id":"ENSG00000110887.7","gene_symbol":"DAO","gene_name":"D-amino acid oxidase [Source:HGNC Symbol;Acc:HGNC:2671]","synonyms":"DAMOX","biotype":"protein_coding","ncbi_id":"1610","summary":"This gene encodes the peroxisomal enzyme D-amino acid oxidase. The enzyme is a flavoprotein which uses flavin adenine dinucleotide (FAD) as its prosthetic group. Its substrates include a wide variety of D-amino acids, but it is inactive on the naturally occurring L-amino acids. Its biological function is not known; it may act as a detoxifying agent which removes D-amino acids that accumulate during aging. In mice, it degrades D-serine, a co-agonist of the NMDA receptor. This gene may play a role in the pathophysiology of schizophrenia. [provided by RefSeq, Jul 2008]","start":108858932,"end":108901043,"strand":1,"description":"D-amino acid oxidase [Source:HGNC Symbol;Acc:HGNC:2671]"}, {"versioned_ensembl_gene_id":"ENSG00000087008.15","gene_symbol":"ACOX3","gene_name":"acyl-CoA oxidase 3, pristanoyl [Source:HGNC Symbol;Acc:HGNC:121]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8310","summary":"Acyl-Coenzyme A oxidase 3 also know as pristanoyl -CoA oxidase (ACOX3)is involved in the desaturation of 2-methyl branched fatty acids in peroxisomes. Unlike the rat homolog, the human gene is expressed in very low amounts in liver such that its mRNA was undetectable by routine Northern-blot analysis or its product by immunoblotting or by enzyme activity measurements. However the human cDNA encoding a 700 amino acid protein with a peroxisomal targeting C-terminal tripeptide S-K-L was isolated and is thought to be expressed under special conditions such as specific developmental stages or in a tissue specific manner in tissues that have not yet been examined. [provided by RefSeq, Jul 2008]","start":8366282,"end":8440723,"strand":-1,"description":"acyl-CoA oxidase 3, pristanoyl [Source:HGNC Symbol;Acc:HGNC:121]"}, {"versioned_ensembl_gene_id":"ENSG00000257477.1","gene_symbol":"LINC01154","gene_name":"long intergenic non-protein coding RNA 1154 [Source:HGNC Symbol;Acc:HGNC:49504]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144575","summary":null,"start":54428303,"end":54429403,"strand":1,"description":"long intergenic non-protein coding RNA 1154 [Source:HGNC Symbol;Acc:HGNC:49504]"}, {"versioned_ensembl_gene_id":"ENSG00000163374.19","gene_symbol":"YY1AP1","gene_name":"YY1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30935]","synonyms":"YY1AP,YAP,HCCA2","biotype":"protein_coding","ncbi_id":"55249","summary":"The encoded gene product presumably interacts with YY1 protein; however, its exact function is not known. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":155659443,"end":155689000,"strand":-1,"description":"YY1 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:30935]"}, {"versioned_ensembl_gene_id":"ENSG00000261117.1","gene_symbol":"AC009486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12715415,"end":12716227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211787.1","gene_symbol":"TRAV8-3","gene_name":"T-cell receptor alpha variable 8-3 [Source:HGNC Symbol;Acc:HGNC:12148]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28683","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21852558,"end":21853006,"strand":1,"description":"T-cell receptor alpha variable 8-3 [Source:HGNC Symbol;Acc:HGNC:12148]"}, {"versioned_ensembl_gene_id":"ENSG00000236083.1","gene_symbol":"OR13E1P","gene_name":"olfactory receptor family 13 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15107]","synonyms":"OR13E2,OST741","biotype":"unitary_pseudogene","ncbi_id":"392308","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":35859062,"end":35859983,"strand":-1,"description":"olfactory receptor family 13 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15107]"}, {"versioned_ensembl_gene_id":"ENSG00000215447.7","gene_symbol":"BX322557.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45288052,"end":45291738,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251209.7","gene_symbol":"LINC00923","gene_name":"long intergenic non-protein coding RNA 923 [Source:HGNC Symbol;Acc:HGNC:28088]","synonyms":null,"biotype":"lincRNA","ncbi_id":"91948","summary":null,"start":97572185,"end":97874550,"strand":-1,"description":"long intergenic non-protein coding RNA 923 [Source:HGNC Symbol;Acc:HGNC:28088]"}, {"versioned_ensembl_gene_id":"ENSG00000277513.1","gene_symbol":"AL161637.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43104086,"end":43104497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144962.6","gene_symbol":"SPATA16","gene_name":"spermatogenesis associated 16 [Source:HGNC Symbol;Acc:HGNC:29935]","synonyms":"NYD-SP12","biotype":"protein_coding","ncbi_id":"83893","summary":"This gene encodes a testis-specific protein that belongs to the tetratricopeptide repeat-like superfamily. The encoded protein localizes to the Golgi apparatus and may play a role in spermatogenesis. [provided by RefSeq, May 2010]","start":172889358,"end":173141268,"strand":-1,"description":"spermatogenesis associated 16 [Source:HGNC Symbol;Acc:HGNC:29935]"}, {"versioned_ensembl_gene_id":"ENSG00000182541.17","gene_symbol":"LIMK2","gene_name":"LIM domain kinase 2 [Source:HGNC Symbol;Acc:HGNC:6614]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3985","summary":"There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. The protein encoded by this gene is phosphorylated and activated by ROCK, a downstream effector of Rho, and the encoded protein, in turn, phosphorylates cofilin, inhibiting its actin-depolymerizing activity. It is thought that this pathway contributes to Rho-induced reorganization of the actin cytoskeleton. At least three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31212239,"end":31280080,"strand":1,"description":"LIM domain kinase 2 [Source:HGNC Symbol;Acc:HGNC:6614]"}, {"versioned_ensembl_gene_id":"ENSG00000243885.1","gene_symbol":"AC108751.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149384179,"end":149385800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140157.14","gene_symbol":"NIPA2","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 2 [Source:HGNC Symbol;Acc:HGNC:17044]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81614","summary":"This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]","start":22838641,"end":22868384,"strand":1,"description":"non imprinted in Prader-Willi/Angelman syndrome 2 [Source:HGNC Symbol;Acc:HGNC:17044]"}, {"versioned_ensembl_gene_id":"ENSG00000243753.5","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLAL,HLA92,HLA-92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30259584,"end":30293014,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000225578.1","gene_symbol":"NCBP2-AS1","gene_name":"NCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40392]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874001","summary":null,"start":196939877,"end":196942534,"strand":1,"description":"NCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40392]"}, {"versioned_ensembl_gene_id":"ENSG00000170946.14","gene_symbol":"DNAJC24","gene_name":"DnaJ heat shock protein family (Hsp40) member C24 [Source:HGNC Symbol;Acc:HGNC:26979]","synonyms":"ZCSL3,JJJ3,DPH4","biotype":"protein_coding","ncbi_id":"120526","summary":"Diphthamide is a unique posttranslationally modified histidine found only in translation elongation factor-2 (EEF2; MIM 130610). This modification is conserved from archaebacteria to humans and serves as the target for ADP-ribosylation and inactivation of EEF2 by diphtheria toxin (DT) and Pseudomonas exotoxin A. DPH4 is 1 of several enzymes involved in synthesis of diphthamide in EEF2 (Liu et al., 2004 [PubMed 15485916]).[supplied by OMIM, Mar 2008]","start":31369840,"end":31431849,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C24 [Source:HGNC Symbol;Acc:HGNC:26979]"}, {"versioned_ensembl_gene_id":"ENSG00000240541.2","gene_symbol":"TM4SF1-AS1","gene_name":"TM4SF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40587]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874091","summary":null,"start":149377778,"end":149386583,"strand":1,"description":"TM4SF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40587]"}, {"versioned_ensembl_gene_id":"ENSG00000277964.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803571,"end":54814487,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000228626.1","gene_symbol":"AC245100.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148288001,"end":148288951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278489.2","gene_symbol":"KRTAP5-2","gene_name":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]","synonyms":"KRTAP5.2,KRTAP5-8","biotype":"protein_coding","ncbi_id":"440021","summary":null,"start":1602887,"end":1604004,"strand":-1,"description":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]"}, {"versioned_ensembl_gene_id":"ENSG00000151233.10","gene_symbol":"GXYLT1","gene_name":"glucoside xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27482]","synonyms":"GLT8D3,FLJ43151","biotype":"protein_coding","ncbi_id":"283464","summary":"GXYLT1 is a xylosyltransferase (EC 2.4.2.-) that adds the first xylose to O-glucose-modified residues in the epidermal growth factor (EGF; MIM 131530) repeats of proteins such as NOTCH1 (MIM 190198) (Sethi et al., 2010 [PubMed 19940119]).[supplied by OMIM, Mar 2010]","start":42081845,"end":42144879,"strand":-1,"description":"glucoside xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:27482]"}, {"versioned_ensembl_gene_id":"ENSG00000225637.1","gene_symbol":"AP001046.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43363332,"end":43366566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157193.15","gene_symbol":"LRP8","gene_name":"LDL receptor related protein 8 [Source:HGNC Symbol;Acc:HGNC:6700]","synonyms":"MCI1,LRP-8,HSZ75190,APOER2","biotype":"protein_coding","ncbi_id":"7804","summary":"This gene encodes a member of the low density lipoprotein receptor (LDLR) family. Low density lipoprotein receptors are cell surface proteins that play roles in both signal transduction and receptor-mediated endocytosis of specific ligands for lysosomal degradation. The encoded protein plays a critical role in the migration of neurons during development by mediating Reelin signaling, and also functions as a receptor for the cholesterol transport protein apolipoprotein E. Expression of this gene may be a marker for major depressive disorder. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":53242364,"end":53328070,"strand":-1,"description":"LDL receptor related protein 8 [Source:HGNC Symbol;Acc:HGNC:6700]"}, {"versioned_ensembl_gene_id":"ENSG00000206120.11","gene_symbol":"EGFEM1P","gene_name":"EGF like and EMI domain containing 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:25149]","synonyms":"NCRNA00259,C3orf50","biotype":"transcribed_unitary_pseudogene","ncbi_id":"93556","summary":null,"start":168249522,"end":168830599,"strand":1,"description":"EGF like and EMI domain containing 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:25149]"}, {"versioned_ensembl_gene_id":"ENSG00000276247.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000279548.1","gene_symbol":"AL022323.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25022594,"end":25024652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283573.1","gene_symbol":"AL157371.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43803193,"end":43842625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261305.1","gene_symbol":"AC005586.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":150341771,"end":150342607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266279.1","gene_symbol":"AC135178.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8337697,"end":8338758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228666.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28969130,"end":28970460,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000234846.7","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31850351,"end":31855624,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000227740.1","gene_symbol":"AL513329.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175904762,"end":175920513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232857.2","gene_symbol":"KATNBL1P2","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130235","summary":null,"start":94650544,"end":94651378,"strand":-1,"description":"katanin regulatory subunit B1 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49052]"}, {"versioned_ensembl_gene_id":"ENSG00000224851.1","gene_symbol":"LINC00502","gene_name":"long intergenic non-protein coding RNA 502 [Source:HGNC Symbol;Acc:HGNC:43442]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874184","summary":null,"start":91047166,"end":91062159,"strand":1,"description":"long intergenic non-protein coding RNA 502 [Source:HGNC Symbol;Acc:HGNC:43442]"}, {"versioned_ensembl_gene_id":"ENSG00000220585.4","gene_symbol":"DDX18P6","gene_name":"DEAD-box helicase 18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31126]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131370","summary":null,"start":91053051,"end":91055047,"strand":1,"description":"DEAD-box helicase 18 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:31126]"}, {"versioned_ensembl_gene_id":"ENSG00000223761.1","gene_symbol":"AL138767.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87591607,"end":87606024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259631.1","gene_symbol":"AC104316.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122977026,"end":122985629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271440.1","gene_symbol":"AL121932.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28633381,"end":28633594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253439.1","gene_symbol":"CDC42P5","gene_name":"cell division cycle 42 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44429]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507354","summary":null,"start":173085342,"end":173086210,"strand":-1,"description":"cell division cycle 42 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44429]"}, {"versioned_ensembl_gene_id":"ENSG00000099715.14","gene_symbol":"PCDH11Y","gene_name":"protocadherin 11 Y-linked [Source:HGNC Symbol;Acc:HGNC:15813]","synonyms":"PCDHY,PCDH22","biotype":"protein_coding","ncbi_id":"83259","summary":"This gene belongs to the protocadherin family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing seven cadherin repeats, a transmembrane domain, and a cytoplasmic tail that differs from those of the classical cadherins. This gene is located on the Y chromosome in a block of X/Y homology and is very closely related to its paralog on the X chromosome. The protein is thought to play a role in cell-cell recognition during development of the central nervous system. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":5000226,"end":5742224,"strand":1,"description":"protocadherin 11 Y-linked [Source:HGNC Symbol;Acc:HGNC:15813]"}, {"versioned_ensembl_gene_id":"ENSG00000233402.1","gene_symbol":"TARDBPP1","gene_name":"TAR DNA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16536]","synonyms":"TARDBPL,bA318P23.1","biotype":"processed_pseudogene","ncbi_id":"643503","summary":null,"start":6200989,"end":6202191,"strand":-1,"description":"TAR DNA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16536]"}, {"versioned_ensembl_gene_id":"ENSG00000198945.7","gene_symbol":"L3MBTL3","gene_name":"L3MBTL3, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:23035]","synonyms":"KIAA1798","biotype":"protein_coding","ncbi_id":"84456","summary":"This gene encodes a member of the malignant brain tumor (MBT) family of chromatin interacting transcriptional repressors. Members of this family function as methyl-lysine readers, which recognize methylated lysine residues on histone protein tails, and are associated with the repression of gene expression. The encoded protein may regulate hematopoiesis. Homozygous deletion of this gene has been observed in human patients with medulloblastoma. [provided by RefSeq, Oct 2016]","start":130013699,"end":130141451,"strand":1,"description":"L3MBTL3, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:23035]"}, {"versioned_ensembl_gene_id":"ENSG00000259283.2","gene_symbol":"AC109462.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55259969,"end":55333588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158516.11","gene_symbol":"CPA2","gene_name":"carboxypeptidase A2 [Source:HGNC Symbol;Acc:HGNC:2297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1358","summary":"Three different forms of human pancreatic procarboxypeptidase A have been isolated. The encoded protein represents the A2 form, which is a monomeric protein with different biochemical properties from the A1 and A3 forms. The A2 form of pancreatic procarboxypeptidase acts on aromatic C-terminal residues and is a secreted protein. [provided by RefSeq, Dec 2008]","start":130266827,"end":130289798,"strand":1,"description":"carboxypeptidase A2 [Source:HGNC Symbol;Acc:HGNC:2297]"}, {"versioned_ensembl_gene_id":"ENSG00000183674.11","gene_symbol":"LINC00518","gene_name":"long intergenic non-protein coding RNA 518 [Source:HGNC Symbol;Acc:HGNC:28626]","synonyms":"MGC40222,C6orf218","biotype":"lincRNA","ncbi_id":"221718","summary":null,"start":10429255,"end":10434874,"strand":-1,"description":"long intergenic non-protein coding RNA 518 [Source:HGNC Symbol;Acc:HGNC:28626]"}, {"versioned_ensembl_gene_id":"ENSG00000213856.3","gene_symbol":"VDAC1P2","gene_name":"voltage dependent anion channel 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12670]","synonyms":"VDAC1LP","biotype":"processed_pseudogene","ncbi_id":"10064","summary":null,"start":49632500,"end":49633349,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12670]"}, {"versioned_ensembl_gene_id":"ENSG00000168589.14","gene_symbol":"DYNLRB2","gene_name":"dynein light chain roadblock-type 2 [Source:HGNC Symbol;Acc:HGNC:15467]","synonyms":"ROBLD2,DNLC2B,DNCL2B","biotype":"protein_coding","ncbi_id":"83657","summary":null,"start":80540734,"end":80550760,"strand":1,"description":"dynein light chain roadblock-type 2 [Source:HGNC Symbol;Acc:HGNC:15467]"}, {"versioned_ensembl_gene_id":"ENSG00000259043.1","gene_symbol":"BRD7P1","gene_name":"bromodomain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19923]","synonyms":"BRD7P","biotype":"processed_pseudogene","ncbi_id":"100288948","summary":null,"start":23749236,"end":23751150,"strand":1,"description":"bromodomain containing 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19923]"}, {"versioned_ensembl_gene_id":"ENSG00000260183.1","gene_symbol":"AC108097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80547842,"end":80552514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239713.8","gene_symbol":"APOBEC3G","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3G [Source:HGNC Symbol;Acc:HGNC:17357]","synonyms":"MDS019,FLJ12740,dJ494G10.1,CEM15,bK150C2.7","biotype":"protein_coding","ncbi_id":"60489","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. The protein encoded by this gene catalyzes site-specific deamination of both RNA and single-stranded DNA. The encoded protein has been found to be a specific inhibitor of human immunodeficiency virus-1 (HIV-1) infectivity. [provided by RefSeq, Mar 2017]","start":39077005,"end":39087743,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3G [Source:HGNC Symbol;Acc:HGNC:17357]"}, {"versioned_ensembl_gene_id":"ENSG00000134548.9","gene_symbol":"SPX","gene_name":"spexin hormone [Source:HGNC Symbol;Acc:HGNC:28139]","synonyms":"MGC10946,C12orf39,spexin,NPQ","biotype":"protein_coding","ncbi_id":"80763","summary":"The protein encoded by this gene is a hormone involved in modulation of cardiovascular and renal function. It has also been shown in rats to cause weight loss. Several transcript variants have been found for this gene. [provided by RefSeq, Feb 2016]","start":21526307,"end":21537377,"strand":1,"description":"spexin hormone [Source:HGNC Symbol;Acc:HGNC:28139]"}, {"versioned_ensembl_gene_id":"ENSG00000272342.1","gene_symbol":"LINC01115","gene_name":"long intergenic non-protein coding RNA 1115 [Source:NCBI gene;Acc:339822]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339822","summary":null,"start":739588,"end":740164,"strand":-1,"description":"long intergenic non-protein coding RNA 1115 [Source:NCBI gene;Acc:339822]"}, {"versioned_ensembl_gene_id":"ENSG00000281769.1","gene_symbol":"LINC01230","gene_name":"long intergenic non-protein coding RNA 1230 [Source:HGNC Symbol;Acc:HGNC:49686]","synonyms":"TCONS_00015639,lnc-DRMT2,linc-DMRT2","biotype":"lincRNA","ncbi_id":"102800446","summary":null,"start":1045625,"end":1048641,"strand":1,"description":"long intergenic non-protein coding RNA 1230 [Source:HGNC Symbol;Acc:HGNC:49686]"}, {"versioned_ensembl_gene_id":"ENSG00000245025.2","gene_symbol":"AC107959.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22984596,"end":23019335,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228783.1","gene_symbol":"AL358976.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1011085,"end":1011799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154678.16","gene_symbol":"PDE1C","gene_name":"phosphodiesterase 1C [Source:HGNC Symbol;Acc:HGNC:8776]","synonyms":"Hcam3","biotype":"protein_coding","ncbi_id":"5137","summary":"This gene encodes an enzyme that belongs to the 3'5'-cyclic nucleotide phosphodiesterase family. Members of this family catalyze hydrolysis of the cyclic nucleotides, cyclic adenosine monophosphate and cyclic guanosine monophosphate, to the corresponding nucleoside 5'-monophosphates. The enzyme encoded by this gene regulates proliferation and migration of vascular smooth muscle cells, and neointimal hyperplasia. This enzyme also plays a role in pathological vascular remodeling by regulating the stability of growth factor receptors, such as PDGF-receptor-beta. [provided by RefSeq, Jul 2016]","start":31751179,"end":32299329,"strand":-1,"description":"phosphodiesterase 1C [Source:HGNC Symbol;Acc:HGNC:8776]"}, {"versioned_ensembl_gene_id":"ENSG00000148677.6","gene_symbol":"ANKRD1","gene_name":"ankyrin repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:15819]","synonyms":"C-193,ALRP,MCARP,CVARP,CARP","biotype":"protein_coding","ncbi_id":"27063","summary":"The protein encoded by this gene is localized to the nucleus of endothelial cells and is induced by IL-1 and TNF-alpha stimulation. Studies in rat cardiomyocytes suggest that this gene functions as a transcription factor. Interactions between this protein and the sarcomeric proteins myopalladin and titin suggest that it may also be involved in the myofibrillar stretch-sensor system. [provided by RefSeq, Jul 2008]","start":90912096,"end":90921276,"strand":-1,"description":"ankyrin repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:15819]"}, {"versioned_ensembl_gene_id":"ENSG00000155755.18","gene_symbol":"TMEM237","gene_name":"transmembrane protein 237 [Source:HGNC Symbol;Acc:HGNC:14432]","synonyms":"JBTS14,ALS2CR4","biotype":"protein_coding","ncbi_id":"65062","summary":"The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":201620184,"end":201643570,"strand":-1,"description":"transmembrane protein 237 [Source:HGNC Symbol;Acc:HGNC:14432]"}, {"versioned_ensembl_gene_id":"ENSG00000143067.4","gene_symbol":"ZNF697","gene_name":"zinc finger protein 697 [Source:HGNC Symbol;Acc:HGNC:32034]","synonyms":"MGC45731","biotype":"protein_coding","ncbi_id":"90874","summary":null,"start":119619422,"end":119647773,"strand":-1,"description":"zinc finger protein 697 [Source:HGNC Symbol;Acc:HGNC:32034]"}, {"versioned_ensembl_gene_id":"ENSG00000261646.1","gene_symbol":"AC093849.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173467833,"end":173470041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135838.13","gene_symbol":"NPL","gene_name":"N-acetylneuraminate pyruvate lyase [Source:HGNC Symbol;Acc:HGNC:16781]","synonyms":"NPL1,DHDPS1,C1orf13","biotype":"protein_coding","ncbi_id":"80896","summary":"This gene encodes a member of the N-acetylneuraminate lyase sub-family of (beta/alpha)(8)-barrel enzymes. N-acetylneuraminate lyases regulate cellular concentrations of N-acetyl-neuraminic acid (sialic acid) by mediating the reversible conversion of sialic acid into N-acetylmannosamine and pyruvate. A pseudogene of this gene is located on the short arm of chromosome 2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":182789293,"end":182830384,"strand":1,"description":"N-acetylneuraminate pyruvate lyase [Source:HGNC Symbol;Acc:HGNC:16781]"}, {"versioned_ensembl_gene_id":"ENSG00000267764.1","gene_symbol":"AC093567.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48826051,"end":48834770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114353.16","gene_symbol":"GNAI2","gene_name":"G protein subunit alpha i2 [Source:HGNC Symbol;Acc:HGNC:4385]","synonyms":"GNAI2B,GIP","biotype":"protein_coding","ncbi_id":"2771","summary":"The protein encoded by this gene is an alpha subunit of guanine nucleotide binding proteins (G proteins). The encoded protein contains the guanine nucleotide binding site and is involved in the hormonal regulation of adenylate cyclase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":50226292,"end":50259355,"strand":1,"description":"G protein subunit alpha i2 [Source:HGNC Symbol;Acc:HGNC:4385]"}, {"versioned_ensembl_gene_id":"ENSG00000260876.5","gene_symbol":"LINC01229","gene_name":"long intergenic non-protein coding RNA 1229 [Source:HGNC Symbol;Acc:HGNC:49682]","synonyms":"TCONS_00024480","biotype":"lincRNA","ncbi_id":"101928248","summary":null,"start":79676108,"end":79807922,"strand":1,"description":"long intergenic non-protein coding RNA 1229 [Source:HGNC Symbol;Acc:HGNC:49682]"}, {"versioned_ensembl_gene_id":"ENSG00000224140.2","gene_symbol":"TNXA","gene_name":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]","synonyms":"TNX,HXBL,D6S103E,XA","biotype":"unprocessed_pseudogene","ncbi_id":"7146","summary":null,"start":32085057,"end":32088915,"strand":-1,"description":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]"}, {"versioned_ensembl_gene_id":"ENSG00000114790.12","gene_symbol":"ARHGEF26","gene_name":"Rho guanine nucleotide exchange factor 26 [Source:HGNC Symbol;Acc:HGNC:24490]","synonyms":"SGEF,DKFZP434D146","biotype":"protein_coding","ncbi_id":"26084","summary":"This gene encodes a member of the Rho-guanine nucleotide exchange factor (Rho-GEF) family. These proteins regulate Rho GTPases by catalyzing the exchange of GDP for GTP. The encoded protein specifically activates RhoG and plays a role in the promotion of macropinocytosis. Underexpression of the encoded protein may be a predictive marker of chemoresistant disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":154121003,"end":154257827,"strand":1,"description":"Rho guanine nucleotide exchange factor 26 [Source:HGNC Symbol;Acc:HGNC:24490]"}, {"versioned_ensembl_gene_id":"ENSG00000275285.1","gene_symbol":"AL391095.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38378825,"end":38383179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273722.4","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160592,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000237876.1","gene_symbol":"AKR1B1P4","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:423]","synonyms":"ALDRL4","biotype":"processed_pseudogene","ncbi_id":"390402","summary":null,"start":45687548,"end":45688469,"strand":-1,"description":"aldo-keto reductase family 1 member B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:423]"}, {"versioned_ensembl_gene_id":"ENSG00000277558.1","gene_symbol":"AL109923.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34476205,"end":34476787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174279.4","gene_symbol":"EVX2","gene_name":"even-skipped homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3507]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344191","summary":"This gene is located at the 5' end of the HOXD gene cluster on chromosome 2. The encoded protein is a homeobox transcription factor that is related to the protein encoded by the Drosophila even-skipped (eve) gene, a member of the pair-rule class of segmentation genes. A 117 kb microdeletion at the 5' end of the HOXD gene cluster, which includes this gene and the HOXD9-HOXD13 genes, causes synpolydactyly, a dominantly inherited disease resulting in limb malformation. [provided by RefSeq, Sep 2009]","start":176077472,"end":176083913,"strand":-1,"description":"even-skipped homeobox 2 [Source:HGNC Symbol;Acc:HGNC:3507]"}, {"versioned_ensembl_gene_id":"ENSG00000228779.1","gene_symbol":"Z69666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":125737,"end":127219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234470.1","gene_symbol":"CR753841.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32501548,"end":32501955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280593.1","gene_symbol":"AL732314.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":389670,"end":408269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196230.12","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30720201,"end":30725426,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000216809.1","gene_symbol":"AL589993.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118452469,"end":118454992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174106.2","gene_symbol":"LEMD3","gene_name":"LEM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28887]","synonyms":"MAN1","biotype":"protein_coding","ncbi_id":"23592","summary":"This locus encodes a LEM domain-containing protein. The encoded protein functions to antagonize transforming growth factor-beta signaling at the inner nuclear membrane. Two transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.[provided by RefSeq, Nov 2009]","start":65169571,"end":65248327,"strand":1,"description":"LEM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28887]"}, {"versioned_ensembl_gene_id":"ENSG00000276853.1","gene_symbol":"AC026124.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65171262,"end":65171917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170891.10","gene_symbol":"CYTL1","gene_name":"cytokine like 1 [Source:HGNC Symbol;Acc:HGNC:24435]","synonyms":"C4orf4,C17","biotype":"protein_coding","ncbi_id":"54360","summary":"C17 is a cytokine-like protein specifically expressed in bone marrow and cord blood mononuclear cells that bear the CD34 (MIM 142230) surface marker (Liu et al., 2000 [PubMed 10857752]).[supplied by OMIM, Mar 2008]","start":5014586,"end":5019472,"strand":-1,"description":"cytokine like 1 [Source:HGNC Symbol;Acc:HGNC:24435]"}, {"versioned_ensembl_gene_id":"ENSG00000228314.1","gene_symbol":"CYP4F29P","gene_name":"cytochrome P450 family 4 subfamily F member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:2647]","synonyms":"CYP4F3LP,CYP4F-se4[6:7:8],C21orf15","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54055","summary":null,"start":13843133,"end":13848364,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:2647]"}, {"versioned_ensembl_gene_id":"ENSG00000261747.3","gene_symbol":"AC120045.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30153933,"end":30154110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157106.16","gene_symbol":"SMG1","gene_name":"SMG1, nonsense mediated mRNA decay associated PI3K related kinase [Source:HGNC Symbol;Acc:HGNC:30045]","synonyms":"LIP,KIAA0421,ATX","biotype":"protein_coding","ncbi_id":"23049","summary":"This gene encodes a protein involved in nonsense-mediated mRNA decay (NMD) as part of the mRNA surveillance complex. The protein has kinase activity and is thought to function in NMD by phosphorylating the regulator of nonsense transcripts 1 protein. Alternatively spliced transcript variants have been described, but their full-length nature has yet to be determined. [provided by RefSeq, Mar 2013]","start":18804853,"end":18926454,"strand":-1,"description":"SMG1, nonsense mediated mRNA decay associated PI3K related kinase [Source:HGNC Symbol;Acc:HGNC:30045]"}, {"versioned_ensembl_gene_id":"ENSG00000277848.4","gene_symbol":"MEGF11","gene_name":"multiple EGF like domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]","synonyms":"DKFZp434L121,KIAA1781","biotype":"protein_coding","ncbi_id":"84465","summary":null,"start":65909030,"end":66265884,"strand":-1,"description":"multiple EGF like domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]"}, {"versioned_ensembl_gene_id":"ENSG00000232284.7","gene_symbol":"GNG12-AS1","gene_name":"GNG12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43938]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289178","summary":null,"start":67832303,"end":68202987,"strand":1,"description":"GNG12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43938]"}, {"versioned_ensembl_gene_id":"ENSG00000115414.18","gene_symbol":"FN1","gene_name":"fibronectin 1 [Source:HGNC Symbol;Acc:HGNC:3778]","synonyms":"MSF,LETS,GFND2,FINC,CIG","biotype":"protein_coding","ncbi_id":"2335","summary":"This gene encodes fibronectin, a glycoprotein present in a soluble dimeric form in plasma, and in a dimeric or multimeric form at the cell surface and in extracellular matrix. The encoded preproprotein is proteolytically processed to generate the mature protein. Fibronectin is involved in cell adhesion and migration processes including embryogenesis, wound healing, blood coagulation, host defense, and metastasis. The gene has three regions subject to alternative splicing, with the potential to produce 20 different transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. The full-length nature of some variants has not been determined. [provided by RefSeq, Jan 2016]","start":215360440,"end":215436172,"strand":-1,"description":"fibronectin 1 [Source:HGNC Symbol;Acc:HGNC:3778]"}, {"versioned_ensembl_gene_id":"ENSG00000233593.8","gene_symbol":"AL590094.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":90782983,"end":90851657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176679.8","gene_symbol":"TGIF2LY","gene_name":"TGFB induced factor homeobox 2 like, Y-linked [Source:HGNC Symbol;Acc:HGNC:18569]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90655","summary":"This gene encodes a member of the TALE/TGIF homeobox family of transcription factors. This gene lies within the male specific region of chromosome Y, in a block of sequence that is thought to be the result of a large X-to-Y transposition. The C-terminus of this protein is divergent from that of its chromosome X homolog (TGIF2LX), suggesting that this protein may act as a regulator of TGIF2LX. [provided by RefSeq, Jul 2008]","start":3579041,"end":3580041,"strand":1,"description":"TGFB induced factor homeobox 2 like, Y-linked [Source:HGNC Symbol;Acc:HGNC:18569]"}, {"versioned_ensembl_gene_id":"ENSG00000143032.7","gene_symbol":"BARHL2","gene_name":"BarH like homeobox 2 [Source:HGNC Symbol;Acc:HGNC:954]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343472","summary":null,"start":90711539,"end":90717237,"strand":-1,"description":"BarH like homeobox 2 [Source:HGNC Symbol;Acc:HGNC:954]"}, {"versioned_ensembl_gene_id":"ENSG00000231574.5","gene_symbol":"LINC02015","gene_name":"long intergenic non-protein coding RNA 2015 [Source:HGNC Symbol;Acc:HGNC:52850]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724550","summary":null,"start":177816865,"end":177899224,"strand":1,"description":"long intergenic non-protein coding RNA 2015 [Source:HGNC Symbol;Acc:HGNC:52850]"}, {"versioned_ensembl_gene_id":"ENSG00000254181.1","gene_symbol":"SLC25A51P3","gene_name":"solute carrier family 25 member 51 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31051]","synonyms":"MCART5P","biotype":"processed_pseudogene","ncbi_id":"100128119","summary":null,"start":80594815,"end":80595703,"strand":-1,"description":"solute carrier family 25 member 51 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31051]"}, {"versioned_ensembl_gene_id":"ENSG00000233971.1","gene_symbol":"RPS20P10","gene_name":"ribosomal protein S20 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271081","summary":null,"start":71984182,"end":71984434,"strand":-1,"description":"ribosomal protein S20 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36800]"}, {"versioned_ensembl_gene_id":"ENSG00000241203.1","gene_symbol":"HMGN2P26","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39393]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874470","summary":null,"start":167958744,"end":167959082,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39393]"}, {"versioned_ensembl_gene_id":"ENSG00000280748.1","gene_symbol":"AC233280.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167191.11","gene_symbol":"GPRC5B","gene_name":"G protein-coupled receptor class C group 5 member B [Source:HGNC Symbol;Acc:HGNC:13308]","synonyms":"RAIG-2","biotype":"protein_coding","ncbi_id":"51704","summary":"This gene encodes a member of the type 3 G protein-coupled receptor family. Members of this superfamily are characterized by a signature 7-transmembrane domain motif. The encoded protein may modulate insulin secretion and increased protein expression is associated with type 2 diabetes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":19856691,"end":19886167,"strand":-1,"description":"G protein-coupled receptor class C group 5 member B [Source:HGNC Symbol;Acc:HGNC:13308]"}, {"versioned_ensembl_gene_id":"ENSG00000273293.1","gene_symbol":"AC093458.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149881359,"end":149881580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233892.1","gene_symbol":"AL671855.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30186798,"end":30188614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103550.13","gene_symbol":"KNOP1","gene_name":"lysine rich nucleolar protein 1 [Source:HGNC Symbol;Acc:HGNC:34404]","synonyms":"TSG118,FAM191A,C16orf88,101F10.1","biotype":"protein_coding","ncbi_id":"400506","summary":"The protein encoded by this gene is a nucleolar protein that interacts with zinc finger 106 protein. The encoded protein has several of the same characteristics as nucleostemin and may be involved in testis development. [provided by RefSeq, Feb 2017]","start":19701934,"end":19718235,"strand":-1,"description":"lysine rich nucleolar protein 1 [Source:HGNC Symbol;Acc:HGNC:34404]"}, {"versioned_ensembl_gene_id":"ENSG00000165443.11","gene_symbol":"PHYHIPL","gene_name":"phytanoyl-CoA 2-hydroxylase interacting protein like [Source:HGNC Symbol;Acc:HGNC:29378]","synonyms":"KIAA1796,Em:AC025038.1","biotype":"protein_coding","ncbi_id":"84457","summary":null,"start":59176590,"end":59247774,"strand":1,"description":"phytanoyl-CoA 2-hydroxylase interacting protein like [Source:HGNC Symbol;Acc:HGNC:29378]"}, {"versioned_ensembl_gene_id":"ENSG00000124237.5","gene_symbol":"C20orf85","gene_name":"chromosome 20 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:16216]","synonyms":"LLC1,bA196N14.1","biotype":"protein_coding","ncbi_id":"128602","summary":null,"start":58150904,"end":58161150,"strand":1,"description":"chromosome 20 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:16216]"}, {"versioned_ensembl_gene_id":"ENSG00000235115.3","gene_symbol":"CHCHD2P8","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39592]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646630","summary":null,"start":28107431,"end":28107877,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39592]"}, {"versioned_ensembl_gene_id":"ENSG00000257825.1","gene_symbol":"CR383656.10","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18588274,"end":18588315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220291.1","gene_symbol":"AL139806.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85155667,"end":85167749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125166.12","gene_symbol":"GOT2","gene_name":"glutamic-oxaloacetic transaminase 2 [Source:HGNC Symbol;Acc:HGNC:4433]","synonyms":"mitAAT,KYAT4,KATIV,KAT4","biotype":"protein_coding","ncbi_id":"2806","summary":"Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":58707131,"end":58734357,"strand":-1,"description":"glutamic-oxaloacetic transaminase 2 [Source:HGNC Symbol;Acc:HGNC:4433]"}, {"versioned_ensembl_gene_id":"ENSG00000230449.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30696806,"end":30697535,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000257947.1","gene_symbol":"AC025030.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44244394,"end":44263982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244043.1","gene_symbol":"RPS27P27","gene_name":"ribosomal protein S27 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36043]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271585","summary":null,"start":59088837,"end":59089091,"strand":1,"description":"ribosomal protein S27 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36043]"}, {"versioned_ensembl_gene_id":"ENSG00000247735.2","gene_symbol":"AC120114.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29926836,"end":29928933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164548.10","gene_symbol":"TRA2A","gene_name":"transformer 2 alpha homolog [Source:HGNC Symbol;Acc:HGNC:16645]","synonyms":"tra2a,htra-2-alpha,AWMS1","biotype":"protein_coding","ncbi_id":"29896","summary":"This gene is a member of the transformer 2 homolog family and encodes a protein with several RRM (RNA recognition motif) domains. This phosphorylated nuclear protein binds to specific RNA sequences and plays a role in the regulation of pre-mRNA splicing. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]","start":23504780,"end":23532041,"strand":-1,"description":"transformer 2 alpha homolog [Source:HGNC Symbol;Acc:HGNC:16645]"}, {"versioned_ensembl_gene_id":"ENSG00000258773.1","gene_symbol":"AC087636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95080095,"end":95132859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224309.7","gene_symbol":"ANKRD30BP2","gene_name":"ankyrin repeat domain 30B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16620]","synonyms":"CTSP-1,CT85,C21orf99","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"149992","summary":null,"start":13038160,"end":13067033,"strand":1,"description":"ankyrin repeat domain 30B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16620]"}, {"versioned_ensembl_gene_id":"ENSG00000265354.3","gene_symbol":"TIMM23","gene_name":"translocase of inner mitochondrial membrane 23 [Source:HGNC Symbol;Acc:HGNC:17312]","synonyms":"TIM23","biotype":"protein_coding","ncbi_id":"100287932","summary":"The protein encoded by this gene is part of a complex located in the inner mitochondrial membrane that mediates the transport of transit peptide-containing proteins across the membrane. Multiple transcript variants, one protein-coding and others not protein-coding, have been found for this gene. [provided by RefSeq, Jul 2012]","start":45972449,"end":46003734,"strand":1,"description":"translocase of inner mitochondrial membrane 23 [Source:HGNC Symbol;Acc:HGNC:17312]"}, {"versioned_ensembl_gene_id":"ENSG00000154589.6","gene_symbol":"LY96","gene_name":"lymphocyte antigen 96 [Source:HGNC Symbol;Acc:HGNC:17156]","synonyms":"MD-2","biotype":"protein_coding","ncbi_id":"23643","summary":"This gene encodes a protein which associates with toll-like receptor 4 on the cell surface and confers responsiveness to lipopolysaccyaride (LPS), thus providing a link between the receptor and LPS signaling. Studies of the mouse ortholog suggest that this gene may be involved in endotoxin neutralization. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2010]","start":73991352,"end":74029087,"strand":1,"description":"lymphocyte antigen 96 [Source:HGNC Symbol;Acc:HGNC:17156]"}, {"versioned_ensembl_gene_id":"ENSG00000236654.2","gene_symbol":"AC079780.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23480753,"end":23480959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226695.1","gene_symbol":"ANKRD20A10P","gene_name":"ankyrin repeat domain 20 family member A10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39707]","synonyms":"ANKRD20A4P1","biotype":"processed_pseudogene","ncbi_id":"100421422","summary":null,"start":24750657,"end":24752171,"strand":-1,"description":"ankyrin repeat domain 20 family member A10, pseudogene [Source:HGNC Symbol;Acc:HGNC:39707]"}, {"versioned_ensembl_gene_id":"ENSG00000262512.2","gene_symbol":"KRTAP9-4","gene_name":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]","synonyms":"KAP9.4","biotype":"protein_coding","ncbi_id":"85280","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41249619,"end":41250585,"strand":1,"description":"keratin associated protein 9-4 [Source:HGNC Symbol;Acc:HGNC:18902]"}, {"versioned_ensembl_gene_id":"ENSG00000185133.13","gene_symbol":"INPP5J","gene_name":"inositol polyphosphate-5-phosphatase J [Source:HGNC Symbol;Acc:HGNC:8956]","synonyms":"PIPP,PIB5PA,INPP5","biotype":"protein_coding","ncbi_id":"27124","summary":null,"start":31122731,"end":31134696,"strand":1,"description":"inositol polyphosphate-5-phosphatase J [Source:HGNC Symbol;Acc:HGNC:8956]"}, {"versioned_ensembl_gene_id":"ENSG00000160972.9","gene_symbol":"PPP1R16A","gene_name":"protein phosphatase 1 regulatory subunit 16A [Source:HGNC Symbol;Acc:HGNC:14941]","synonyms":"MYPT3,MGC14333","biotype":"protein_coding","ncbi_id":"84988","summary":"Myosin light chain kinase and phosphatase (MLCP) complexes control the phosphorylation states of regulatory myosin light chains, which is crucial for muscle and intracellular movement. MLCPs typically contain a catalytic protein phosphatase 1 (PP1c) subunit, a myosin phosphatase targeting (MYPT) subunit, and another smaller subunit. The protein encoded by this gene represents an MYPT subunit, which is responsible for directing PP1c to its intended targets. However, while the phosphorylation of other MYPT members results in PP1c inactivation, phosphorylation of the encoded protein by protein kinase A results in PP1c activation. [provided by RefSeq, Jan 2020]","start":144477969,"end":144502121,"strand":1,"description":"protein phosphatase 1 regulatory subunit 16A [Source:HGNC Symbol;Acc:HGNC:14941]"}, {"versioned_ensembl_gene_id":"ENSG00000233219.1","gene_symbol":"AC008080.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33868501,"end":33874231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276497.3","gene_symbol":"APBA1","gene_name":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]","synonyms":"X11,MINT1,D9S411E","biotype":"protein_coding","ncbi_id":"320","summary":"The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a putative vesicular trafficking protein in the brain that can form a complex with the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. [provided by RefSeq, Jul 2008]","start":69435727,"end":69484339,"strand":-1,"description":"amyloid beta precursor protein binding family A member 1 [Source:HGNC Symbol;Acc:HGNC:578]"}, {"versioned_ensembl_gene_id":"ENSG00000263229.4","gene_symbol":"KRTAP4-11","gene_name":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]","synonyms":"KRTAP4-14,KAP4.14,KAP4.11","biotype":"protein_coding","ncbi_id":"653240","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Mar 2009]","start":41117663,"end":41118842,"strand":-1,"description":"keratin associated protein 4-11 [Source:HGNC Symbol;Acc:HGNC:18911]"}, {"versioned_ensembl_gene_id":"ENSG00000234409.6","gene_symbol":"CCDC188","gene_name":"coiled-coil domain containing 188 [Source:HGNC Symbol;Acc:HGNC:51899]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388849","summary":null,"start":20148427,"end":20151065,"strand":-1,"description":"coiled-coil domain containing 188 [Source:HGNC Symbol;Acc:HGNC:51899]"}, {"versioned_ensembl_gene_id":"ENSG00000211674.2","gene_symbol":"IGLJ1","gene_name":"immunoglobulin lambda joining 1 [Source:HGNC Symbol;Acc:HGNC:5863]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28833","summary":null,"start":22893692,"end":22893818,"strand":1,"description":"immunoglobulin lambda joining 1 [Source:HGNC Symbol;Acc:HGNC:5863]"}, {"versioned_ensembl_gene_id":"ENSG00000100285.9","gene_symbol":"NEFH","gene_name":"neurofilament heavy [Source:HGNC Symbol;Acc:HGNC:7737]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4744","summary":"Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and functionally maintain neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the heavy neurofilament protein. This protein is commonly used as a biomarker of neuronal damage and susceptibility to amyotrophic lateral sclerosis (ALS) has been associated with mutations in this gene. [provided by RefSeq, Oct 2008]","start":29480230,"end":29491390,"strand":1,"description":"neurofilament heavy [Source:HGNC Symbol;Acc:HGNC:7737]"}, {"versioned_ensembl_gene_id":"ENSG00000225659.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30228578,"end":30232554,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000226614.11","gene_symbol":"SLC39A7","gene_name":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]","synonyms":"ZIP7,HKE4,RING5,H2-KE4,KE4,D6S2244E","biotype":"protein_coding","ncbi_id":"7922","summary":"The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33122069,"end":33126063,"strand":1,"description":"solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]"}, {"versioned_ensembl_gene_id":"ENSG00000184828.9","gene_symbol":"ZBTB7C","gene_name":"zinc finger and BTB domain containing 7C [Source:HGNC Symbol;Acc:HGNC:31700]","synonyms":"ZBTB36,ZNF857C","biotype":"protein_coding","ncbi_id":"201501","summary":null,"start":48026673,"end":48410752,"strand":-1,"description":"zinc finger and BTB domain containing 7C [Source:HGNC Symbol;Acc:HGNC:31700]"}, {"versioned_ensembl_gene_id":"ENSG00000226181.1","gene_symbol":"AL132671.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117451130,"end":117453525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187682.2","gene_symbol":"ERAS","gene_name":"ES cell expressed Ras [Source:HGNC Symbol;Acc:HGNC:5174]","synonyms":"HRASP,HRAS2","biotype":"protein_coding","ncbi_id":"3266","summary":"This gene encodes a constitutively active member of the small GTPase Ras protein family. The encoded protein activates the phosphatidylinositol 3-kinase signal transduction pathway in undifferentiated stem cells, but is not expressed in differentiated cells. This gene may be involved in cancer and chemotherapy resistance. [provided by RefSeq, Dec 2012]","start":48826513,"end":48830138,"strand":1,"description":"ES cell expressed Ras [Source:HGNC Symbol;Acc:HGNC:5174]"}, {"versioned_ensembl_gene_id":"ENSG00000244321.1","gene_symbol":"LINC01326","gene_name":"long intergenic non-protein coding RNA 1326 [Source:HGNC Symbol;Acc:HGNC:50532]","synonyms":"TCONS_00005878","biotype":"lincRNA","ncbi_id":"106144540","summary":null,"start":166569693,"end":166570763,"strand":-1,"description":"long intergenic non-protein coding RNA 1326 [Source:HGNC Symbol;Acc:HGNC:50532]"}, {"versioned_ensembl_gene_id":"ENSG00000250969.1","gene_symbol":"AC097658.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143286293,"end":143329858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147231.13","gene_symbol":"CXorf57","gene_name":"chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25486]","synonyms":"FLJ14191,FLJ10178","biotype":"protein_coding","ncbi_id":"55086","summary":null,"start":106611930,"end":106679442,"strand":1,"description":"chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:25486]"}, {"versioned_ensembl_gene_id":"ENSG00000242692.1","gene_symbol":"RPS27AP1","gene_name":"ribosomal protein S27a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17121]","synonyms":"RPS27AP","biotype":"processed_pseudogene","ncbi_id":"103911","summary":null,"start":10258762,"end":10259232,"strand":1,"description":"ribosomal protein S27a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17121]"}, {"versioned_ensembl_gene_id":"ENSG00000130038.9","gene_symbol":"CRACR2A","gene_name":"calcium release activated channel regulator 2A [Source:HGNC Symbol;Acc:HGNC:28657]","synonyms":"MGC4266,EFCAB4B","biotype":"protein_coding","ncbi_id":"84766","summary":null,"start":3606633,"end":3764819,"strand":-1,"description":"calcium release activated channel regulator 2A [Source:HGNC Symbol;Acc:HGNC:28657]"}, {"versioned_ensembl_gene_id":"ENSG00000243020.1","gene_symbol":"RPL7P39","gene_name":"ribosomal protein L7 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36214]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271217","summary":null,"start":64867956,"end":64868699,"strand":-1,"description":"ribosomal protein L7 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36214]"}, {"versioned_ensembl_gene_id":"ENSG00000274676.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5,KIR2DL5,CD158F,KIR2DL5.1,CD158F,KIR2DL5.1","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819459,"end":54828923,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000211667.3","gene_symbol":"IGLV3-12","gene_name":"immunoglobulin lambda variable 3-12 [Source:HGNC Symbol;Acc:HGNC:5898]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28802","summary":null,"start":22771824,"end":22772582,"strand":1,"description":"immunoglobulin lambda variable 3-12 [Source:HGNC Symbol;Acc:HGNC:5898]"}, {"versioned_ensembl_gene_id":"ENSG00000041988.15","gene_symbol":"THAP3","gene_name":"THAP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90326","summary":null,"start":6624866,"end":6635586,"strand":1,"description":"THAP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:20855]"}, {"versioned_ensembl_gene_id":"ENSG00000187736.12","gene_symbol":"NHEJ1","gene_name":"non-homologous end joining factor 1 [Source:HGNC Symbol;Acc:HGNC:25737]","synonyms":"XLF,FLJ12610,Cernunnos","biotype":"protein_coding","ncbi_id":"79840","summary":"Double-strand breaks in DNA result from genotoxic stresses and are among the most damaging of DNA lesions. This gene encodes a DNA repair factor essential for the nonhomologous end-joining pathway, which preferentially mediates repair of double-stranded breaks. Mutations in this gene cause different kinds of severe combined immunodeficiency disorders. [provided by RefSeq, Jul 2008]","start":219075317,"end":219160865,"strand":-1,"description":"non-homologous end joining factor 1 [Source:HGNC Symbol;Acc:HGNC:25737]"}, {"versioned_ensembl_gene_id":"ENSG00000211666.2","gene_symbol":"IGLV2-14","gene_name":"immunoglobulin lambda variable 2-14 [Source:HGNC Symbol;Acc:HGNC:5888]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28815","summary":null,"start":22758700,"end":22759218,"strand":1,"description":"immunoglobulin lambda variable 2-14 [Source:HGNC Symbol;Acc:HGNC:5888]"}, {"versioned_ensembl_gene_id":"ENSG00000230735.1","gene_symbol":"AC093423.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89629725,"end":89676386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178457.3","gene_symbol":"LINC00314","gene_name":"long intergenic non-protein coding RNA 314 [Source:HGNC Symbol;Acc:HGNC:16622]","synonyms":"NCRNA00314,C21orf94","biotype":"lincRNA","ncbi_id":"246705","summary":null,"start":28013363,"end":28023233,"strand":1,"description":"long intergenic non-protein coding RNA 314 [Source:HGNC Symbol;Acc:HGNC:16622]"}, {"versioned_ensembl_gene_id":"ENSG00000211661.2","gene_symbol":"IGLV3-22","gene_name":"immunoglobulin lambda variable 3-22 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5906]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28795","summary":null,"start":22704265,"end":22704822,"strand":1,"description":"immunoglobulin lambda variable 3-22 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5906]"}, {"versioned_ensembl_gene_id":"ENSG00000225298.5","gene_symbol":"LINC00113","gene_name":"long intergenic non-protein coding RNA 113 [Source:HGNC Symbol;Acc:HGNC:1264]","synonyms":"NCRNA00113,C21orf23","biotype":"lincRNA","ncbi_id":"54088","summary":null,"start":27722379,"end":27751233,"strand":1,"description":"long intergenic non-protein coding RNA 113 [Source:HGNC Symbol;Acc:HGNC:1264]"}, {"versioned_ensembl_gene_id":"ENSG00000178690.2","gene_symbol":"DYNAP","gene_name":"dynactin associated protein [Source:HGNC Symbol;Acc:HGNC:26808]","synonyms":"FLJ39106,C18orf26","biotype":"protein_coding","ncbi_id":"284254","summary":null,"start":54587757,"end":54599493,"strand":1,"description":"dynactin associated protein [Source:HGNC Symbol;Acc:HGNC:26808]"}, {"versioned_ensembl_gene_id":"ENSG00000230394.1","gene_symbol":"AC078960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8007378,"end":8018160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203989.4","gene_symbol":"RHOXF2B","gene_name":"Rhox homeobox family member 2B [Source:HGNC Symbol;Acc:HGNC:33519]","synonyms":null,"biotype":"protein_coding","ncbi_id":"727940","summary":null,"start":120070672,"end":120077705,"strand":-1,"description":"Rhox homeobox family member 2B [Source:HGNC Symbol;Acc:HGNC:33519]"}, {"versioned_ensembl_gene_id":"ENSG00000225572.1","gene_symbol":"DOCK4-AS1","gene_name":"DOCK4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40876]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506413","summary":null,"start":111808516,"end":111821773,"strand":1,"description":"DOCK4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40876]"}, {"versioned_ensembl_gene_id":"ENSG00000259531.2","gene_symbol":"AC022306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49365124,"end":49366685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253822.1","gene_symbol":"IGLV3-24","gene_name":"immunoglobulin lambda variable 3-24 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5907]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28794","summary":null,"start":22694439,"end":22694952,"strand":1,"description":"immunoglobulin lambda variable 3-24 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5907]"}, {"versioned_ensembl_gene_id":"ENSG00000223999.1","gene_symbol":"AC244250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22692778,"end":22693312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257329.1","gene_symbol":"AC011611.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75964440,"end":75967062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253779.1","gene_symbol":"IGLVVI-25-1","gene_name":"immunoglobulin lambda variable (VI)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15690]","synonyms":"IGLV(VI)-25-1","biotype":"IG_V_pseudogene","ncbi_id":"84090","summary":null,"start":22679097,"end":22679345,"strand":1,"description":"immunoglobulin lambda variable (VI)-25-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15690]"}, {"versioned_ensembl_gene_id":"ENSG00000107185.9","gene_symbol":"RGP1","gene_name":"RGP1 homolog, RAB6A GEF complex partner 1 [Source:HGNC Symbol;Acc:HGNC:21965]","synonyms":"KIAA0258","biotype":"protein_coding","ncbi_id":"9827","summary":null,"start":35749287,"end":35758575,"strand":1,"description":"RGP1 homolog, RAB6A GEF complex partner 1 [Source:HGNC Symbol;Acc:HGNC:21965]"}, {"versioned_ensembl_gene_id":"ENSG00000269176.2","gene_symbol":"AP001160.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62786023,"end":62786785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273712.1","gene_symbol":"AL021997.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28315613,"end":28315883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258140.1","gene_symbol":"AC127894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69212123,"end":69224242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226149.5","gene_symbol":"AL356124.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129526626,"end":129552587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224264.9","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31853814,"end":31872249,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000249462.1","gene_symbol":"MLLT10P2","gene_name":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480724","summary":null,"start":189973599,"end":189973847,"strand":-1,"description":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]"}, {"versioned_ensembl_gene_id":"ENSG00000237814.2","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":31009891,"end":31010713,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000283053.1","gene_symbol":"AL390862.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90622143,"end":90623611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152601.17","gene_symbol":"MBNL1","gene_name":"muscleblind like splicing regulator 1 [Source:HGNC Symbol;Acc:HGNC:6923]","synonyms":"MBNL,KIAA0428,EXP42,EXP40,EXP35,EXP","biotype":"protein_coding","ncbi_id":"4154","summary":"This gene encodes a member of the muscleblind protein family which was initially described in Drosophila melanogaster. The encoded protein is a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Mice lacking this gene exhibited muscle abnormalities and cataracts. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. The different isoforms are thought to have different binding specificities and/or splicing activities. [provided by RefSeq, Sep 2015]","start":152243828,"end":152465780,"strand":1,"description":"muscleblind like splicing regulator 1 [Source:HGNC Symbol;Acc:HGNC:6923]"}, {"versioned_ensembl_gene_id":"ENSG00000223728.3","gene_symbol":"AC239801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147840962,"end":147842359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243964.1","gene_symbol":"RPL23AP65","gene_name":"ribosomal protein L23a pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:36289]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440027","summary":null,"start":9606142,"end":9606609,"strand":1,"description":"ribosomal protein L23a pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:36289]"}, {"versioned_ensembl_gene_id":"ENSG00000163527.9","gene_symbol":"STT3B","gene_name":"STT3B, catalytic subunit of the oligosaccharyltransferase complex [Source:HGNC Symbol;Acc:HGNC:30611]","synonyms":"STT3-B,SIMP,FLJ90106","biotype":"protein_coding","ncbi_id":"201595","summary":"The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]","start":31532638,"end":31637622,"strand":1,"description":"STT3B, catalytic subunit of the oligosaccharyltransferase complex [Source:HGNC Symbol;Acc:HGNC:30611]"}, {"versioned_ensembl_gene_id":"ENSG00000115295.19","gene_symbol":"CLIP4","gene_name":"CAP-Gly domain containing linker protein family member 4 [Source:HGNC Symbol;Acc:HGNC:26108]","synonyms":"RSNL2,FLJ21069","biotype":"protein_coding","ncbi_id":"79745","summary":null,"start":29097705,"end":29189643,"strand":1,"description":"CAP-Gly domain containing linker protein family member 4 [Source:HGNC Symbol;Acc:HGNC:26108]"}, {"versioned_ensembl_gene_id":"ENSG00000135845.9","gene_symbol":"PIGC","gene_name":"phosphatidylinositol glycan anchor biosynthesis class C [Source:HGNC Symbol;Acc:HGNC:8960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5279","summary":"This gene encodes an endoplasmic reticulum associated protein that is involved in glycosylphosphatidylinositol (GPI) lipid anchor biosynthesis. The GPI lipid anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. The encoded protein is one subunit of the GPI N-acetylglucosaminyl (GlcNAc) transferase that transfers GlcNAc to phosphatidylinositol (PI) on the cytoplasmic side of the endoplasmic reticulum. Two alternatively spliced transcripts that encode the same protein have been found for this gene. A pseudogene on chromosome 11 has also been characterized. [provided by RefSeq, Jul 2008]","start":172370189,"end":172444086,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class C [Source:HGNC Symbol;Acc:HGNC:8960]"}, {"versioned_ensembl_gene_id":"ENSG00000271046.1","gene_symbol":"AL512631.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11679675,"end":11680514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267299.1","gene_symbol":"AC011444.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6109322,"end":6125797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251025.1","gene_symbol":"NDUFB5P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52267]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288337","summary":null,"start":180573464,"end":180574027,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52267]"}, {"versioned_ensembl_gene_id":"ENSG00000236929.2","gene_symbol":"AC112498.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15117437,"end":15117768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259244.1","gene_symbol":"AC048382.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":84513241,"end":84526949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171889.3","gene_symbol":"MIR31HG","gene_name":"MIR31 host gene [Source:HGNC Symbol;Acc:HGNC:37187]","synonyms":"LOC554202,hsa-lnc-31","biotype":"sense_overlapping","ncbi_id":"554202","summary":"This gene produces a long non-coding RNA that acts as a host gene for miR-31. This transcript may be involved in cellular pluripotency and regulate the differentiation of myoblasts and other tissues. This RNA was found to interact with Polycomb repressive proteins to repression transcription of genes involves in cell senescence. [provided by RefSeq, Dec 2017]","start":21455642,"end":21559669,"strand":-1,"description":"MIR31 host gene [Source:HGNC Symbol;Acc:HGNC:37187]"}, {"versioned_ensembl_gene_id":"ENSG00000277550.1","gene_symbol":"AL031651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38103524,"end":38104961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228679.1","gene_symbol":"AL034347.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83983728,"end":84007323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229140.8","gene_symbol":"CCDC26","gene_name":"CCDC26 long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:28416]","synonyms":"RAM,MGC27434","biotype":"lincRNA","ncbi_id":"137196","summary":null,"start":129351691,"end":129680239,"strand":-1,"description":"CCDC26 long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:28416]"}, {"versioned_ensembl_gene_id":"ENSG00000230630.4","gene_symbol":"DNM3OS","gene_name":"DNM3 opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:41228]","synonyms":"MIR199A2HG,DNM3-AS1","biotype":"antisense_RNA","ncbi_id":"100628315","summary":null,"start":172136531,"end":172144794,"strand":-1,"description":"DNM3 opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:41228]"}, {"versioned_ensembl_gene_id":"ENSG00000278926.1","gene_symbol":"AC092134.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77800023,"end":77801714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261330.1","gene_symbol":"AC010650.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77892422,"end":77892915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219642.2","gene_symbol":"BMPR1APS1","gene_name":"bone morphogenetic protein receptor type 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421515","summary":null,"start":129157523,"end":129159120,"strand":-1,"description":"bone morphogenetic protein receptor type 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21742]"}, {"versioned_ensembl_gene_id":"ENSG00000162599.15","gene_symbol":"NFIA","gene_name":"nuclear factor I A [Source:HGNC Symbol;Acc:HGNC:7784]","synonyms":"NFI-L,KIAA1439","biotype":"protein_coding","ncbi_id":"4774","summary":"This gene encodes a member of the NF1 (nuclear factor 1) family of transcription factors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":60865259,"end":61462793,"strand":1,"description":"nuclear factor I A [Source:HGNC Symbol;Acc:HGNC:7784]"}, {"versioned_ensembl_gene_id":"ENSG00000135116.9","gene_symbol":"HRK","gene_name":"harakiri, BCL2 interacting protein [Source:HGNC Symbol;Acc:HGNC:5185]","synonyms":"DP5","biotype":"protein_coding","ncbi_id":"8739","summary":"This gene encodes a member of the BCL-2 protein family. Members of this family are involved in activating or inhibiting apoptosis. The encoded protein localizes to intracellular membranes. This protein promotes apoptosis by interacting with the apoptotic inhibitors BCL-2 and BCL-X(L) via its BH3 domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":116856144,"end":116881441,"strand":-1,"description":"harakiri, BCL2 interacting protein [Source:HGNC Symbol;Acc:HGNC:5185]"}, {"versioned_ensembl_gene_id":"ENSG00000270184.1","gene_symbol":"AC018695.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85784382,"end":85787617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198824.5","gene_symbol":"CHAMP1","gene_name":"chromosome alignment maintaining phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:20311]","synonyms":"ZNF828,CHAMP,CAMP,C13orf8","biotype":"protein_coding","ncbi_id":"283489","summary":"This gene encodes a zinc finger protein that functions as a regulator of chromosome segregation in mitosis. The encoded protein is required for correct alignment of chromosomes on the metaphase plate, and plays a role in maintaining the attachment of sister kinetochores to microtubules from opposite spindle poles. Mutations in this gene are associated with an autosomal dominant form of intellectual disability. [provided by RefSeq, Jul 2017]","start":114314513,"end":114327328,"strand":1,"description":"chromosome alignment maintaining phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:20311]"}, {"versioned_ensembl_gene_id":"ENSG00000250100.2","gene_symbol":"AC111000.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69131351,"end":69134814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215908.10","gene_symbol":"CROCCP2","gene_name":"ciliary rootlet coiled-coil, rootletin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:28170]","synonyms":"MGC12760,CROCCL1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"84809","summary":null,"start":16618253,"end":16657232,"strand":-1,"description":"ciliary rootlet coiled-coil, rootletin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:28170]"}, {"versioned_ensembl_gene_id":"ENSG00000115540.14","gene_symbol":"MOB4","gene_name":"MOB family member 4, phocein [Source:HGNC Symbol;Acc:HGNC:17261]","synonyms":"PREI3,PHOCN,MOBKL3,MOB3,DKFZP564M112,CGI-95,2C4D","biotype":"protein_coding","ncbi_id":"25843","summary":"This gene was identified based on its similarity with the mouse counterpart. Studies of the mouse counterpart suggest that the expression of this gene may be regulated during oocyte maturation and preimplantation following zygotic gene activation. Alternatively spliced transcript variants encoding distinct isoforms have been observed. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HSPE1.[provided by RefSeq, Feb 2011]","start":197515571,"end":197553699,"strand":1,"description":"MOB family member 4, phocein [Source:HGNC Symbol;Acc:HGNC:17261]"}, {"versioned_ensembl_gene_id":"ENSG00000077232.17","gene_symbol":"DNAJC10","gene_name":"DnaJ heat shock protein family (Hsp40) member C10 [Source:HGNC Symbol;Acc:HGNC:24637]","synonyms":"PDIA19,ERdj5","biotype":"protein_coding","ncbi_id":"54431","summary":"This gene encodes an endoplasmic reticulum co-chaperone which is part of the endoplasmic reticulum-associated degradation complex involved in recognizing and degrading misfolded proteins. The encoded protein reduces incorrect disulfide bonds in misfolded glycoproteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":182716041,"end":182794464,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C10 [Source:HGNC Symbol;Acc:HGNC:24637]"}, {"versioned_ensembl_gene_id":"ENSG00000254129.1","gene_symbol":"AC108449.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29110573,"end":29140729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196526.10","gene_symbol":"AFAP1","gene_name":"actin filament associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24017]","synonyms":"AFAP-110,AFAP","biotype":"protein_coding","ncbi_id":"60312","summary":"The protein encoded by this gene is a Src binding partner. It may represent a potential modulator of actin filament integrity in response to cellular signals, and may function as an adaptor protein by linking Src family members and/or other signaling proteins to actin filaments. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":7758714,"end":7939926,"strand":-1,"description":"actin filament associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24017]"}, {"versioned_ensembl_gene_id":"ENSG00000187416.11","gene_symbol":"LHFPL3","gene_name":"LHFPL tetraspan subfamily member 3 [Source:HGNC Symbol;Acc:HGNC:6589]","synonyms":"LHFPL4","biotype":"protein_coding","ncbi_id":"375612","summary":"This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008]","start":104328656,"end":104907232,"strand":1,"description":"LHFPL tetraspan subfamily member 3 [Source:HGNC Symbol;Acc:HGNC:6589]"}, {"versioned_ensembl_gene_id":"ENSG00000230685.6","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31717988,"end":31727162,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000230816.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33025668,"end":33029223,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000172361.5","gene_symbol":"CFAP53","gene_name":"cilia and flagella associated protein 53 [Source:HGNC Symbol;Acc:HGNC:26530]","synonyms":"FLJ32743,CCDC11","biotype":"protein_coding","ncbi_id":"220136","summary":"This gene belongs to the CFAP53 family. It was found to be differentially expressed by the ciliated cells of frog epidermis and in skin fibroblasts from human. Mutations in this gene are associated with visceral heterotaxy-6, which implicates this gene in determination of left-right asymmetric patterning. [provided by RefSeq, Aug 2015]","start":50227193,"end":50266522,"strand":-1,"description":"cilia and flagella associated protein 53 [Source:HGNC Symbol;Acc:HGNC:26530]"}, {"versioned_ensembl_gene_id":"ENSG00000267247.1","gene_symbol":"AP005264.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12230411,"end":12231573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236348.1","gene_symbol":"PSMC1P10","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388925","summary":null,"start":17385091,"end":17386417,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39785]"}, {"versioned_ensembl_gene_id":"ENSG00000231217.1","gene_symbol":"AC097347.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6667865,"end":6721544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168818.9","gene_symbol":"STX18","gene_name":"syntaxin 18 [Source:HGNC Symbol;Acc:HGNC:15942]","synonyms":"Ufe1","biotype":"protein_coding","ncbi_id":"53407","summary":"This gene encodes a member of the syntaxin family of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) which is part of a membrane tethering complex that includes other SNAREs and several peripheral membrane proteins, and is involved in vesicular transport between the endoplasmic reticulum (ER) and the Golgi complex. The encoded protein is important for the organization of the smooth, rough, and exit site ER subdomains. A pseudogene of this gene has been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":4415742,"end":4542346,"strand":-1,"description":"syntaxin 18 [Source:HGNC Symbol;Acc:HGNC:15942]"}, {"versioned_ensembl_gene_id":"ENSG00000184985.16","gene_symbol":"SORCS2","gene_name":"sortilin related VPS10 domain containing receptor 2 [Source:HGNC Symbol;Acc:HGNC:16698]","synonyms":"KIAA1329","biotype":"protein_coding","ncbi_id":"57537","summary":"This gene encodes one family member of vacuolar protein sorting 10 (VPS10) domain-containing receptor proteins. The VPS10 domain name comes from the yeast carboxypeptidase Y sorting receptor Vps10 protein. Members of this gene family are large with many exons but the CDS lengths are usually less than 3700 nt. Very large introns typically separate the exons encoding the VPS10 domain; the remaining exons are separated by much smaller-sized introns. These genes are strongly expressed in the central nervous system. [provided by RefSeq, Jul 2008]","start":7192538,"end":7742836,"strand":1,"description":"sortilin related VPS10 domain containing receptor 2 [Source:HGNC Symbol;Acc:HGNC:16698]"}, {"versioned_ensembl_gene_id":"ENSG00000232746.1","gene_symbol":"LINC02022","gene_name":"long intergenic non-protein coding RNA 2022 [Source:HGNC Symbol;Acc:HGNC:52857]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376955","summary":null,"start":12877522,"end":12885211,"strand":-1,"description":"long intergenic non-protein coding RNA 2022 [Source:HGNC Symbol;Acc:HGNC:52857]"}, {"versioned_ensembl_gene_id":"ENSG00000140506.16","gene_symbol":"LMAN1L","gene_name":"lectin, mannose binding 1 like [Source:HGNC Symbol;Acc:HGNC:6632]","synonyms":"ERGL,ERGIC-53L","biotype":"protein_coding","ncbi_id":"79748","summary":"This gene encodes a mannose-binding type 1 transmembrane protein that contains an N-terminal lectin-like carbohydrate recognition domain. The encoded protein is similar in structure to lectins found in leguminous plants. This lectin is thought to transport newly synthesized glycoproteins from the endoplasmic reticulum (ER) to the ER-Golgi intermediate compartment. [provided by RefSeq, Jan 2017]","start":74812716,"end":74825758,"strand":1,"description":"lectin, mannose binding 1 like [Source:HGNC Symbol;Acc:HGNC:6632]"}, {"versioned_ensembl_gene_id":"ENSG00000224059.1","gene_symbol":"HSPA8P16","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:44931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289643","summary":null,"start":85027828,"end":85029692,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:44931]"}, {"versioned_ensembl_gene_id":"ENSG00000262164.6","gene_symbol":"KRT39","gene_name":"keratin 39 [Source:HGNC Symbol;Acc:HGNC:32971]","synonyms":"KA35","biotype":"protein_coding","ncbi_id":"390792","summary":"This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]","start":40958544,"end":40967019,"strand":-1,"description":"keratin 39 [Source:HGNC Symbol;Acc:HGNC:32971]"}, {"versioned_ensembl_gene_id":"ENSG00000137877.9","gene_symbol":"SPTBN5","gene_name":"spectrin beta, non-erythrocytic 5 [Source:HGNC Symbol;Acc:HGNC:15680]","synonyms":"HUSPECV,HUBSPECV,BSPECV","biotype":"protein_coding","ncbi_id":"51332","summary":null,"start":41848144,"end":41894077,"strand":-1,"description":"spectrin beta, non-erythrocytic 5 [Source:HGNC Symbol;Acc:HGNC:15680]"}, {"versioned_ensembl_gene_id":"ENSG00000267733.5","gene_symbol":"AP005264.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":12201982,"end":12223539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267643.1","gene_symbol":"AP005264.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12200779,"end":12201979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278263.2","gene_symbol":"AC135068.2","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":21742364,"end":21742799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185115.5","gene_symbol":"NSMCE3","gene_name":"NSE3 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:7677]","synonyms":"NSE3,NDNL2,MAGEL3,MAGEG1,HCA4","biotype":"protein_coding","ncbi_id":"56160","summary":"The protein encoded by this gene is part of the SMC5-6 chromatin reorganizing complex and is a member of the MAGE superfamily. This is an intronless gene. [provided by RefSeq, May 2011]","start":29264992,"end":29269829,"strand":-1,"description":"NSE3 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:7677]"}, {"versioned_ensembl_gene_id":"ENSG00000281550.1","gene_symbol":"AC135068.9","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":21735506,"end":21735945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169554.18","gene_symbol":"ZEB2","gene_name":"zinc finger E-box binding homeobox 2 [Source:HGNC Symbol;Acc:HGNC:14881]","synonyms":"SIP1,SIP-1,KIAA0569,ZFHX1B","biotype":"protein_coding","ncbi_id":"9839","summary":"The protein encoded by this gene is a member of the Zfh1 family of 2-handed zinc finger/homeodomain proteins. It is located in the nucleus and functions as a DNA-binding transcriptional repressor that interacts with activated SMADs. Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jan 2010]","start":144364364,"end":144524583,"strand":-1,"description":"zinc finger E-box binding homeobox 2 [Source:HGNC Symbol;Acc:HGNC:14881]"}, {"versioned_ensembl_gene_id":"ENSG00000273008.1","gene_symbol":"AC010864.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43136824,"end":43138334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124074.11","gene_symbol":"ENKD1","gene_name":"enkurin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25246]","synonyms":"DKFZP434A1319,C16orf48","biotype":"protein_coding","ncbi_id":"84080","summary":null,"start":67662945,"end":67667265,"strand":-1,"description":"enkurin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25246]"}, {"versioned_ensembl_gene_id":"ENSG00000280227.1","gene_symbol":"AC079416.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53227146,"end":53227694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159761.14","gene_symbol":"C16orf86","gene_name":"chromosome 16 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:33755]","synonyms":"FLJ41802","biotype":"protein_coding","ncbi_id":"388284","summary":null,"start":67666816,"end":67668758,"strand":1,"description":"chromosome 16 open reading frame 86 [Source:HGNC Symbol;Acc:HGNC:33755]"}, {"versioned_ensembl_gene_id":"ENSG00000165312.6","gene_symbol":"OTUD1","gene_name":"OTU deubiquitinase 1 [Source:HGNC Symbol;Acc:HGNC:27346]","synonyms":"OTDC1,DUBA7","biotype":"protein_coding","ncbi_id":"220213","summary":"Deubiquitinating enzymes (DUBs; see MIM 603478) are proteases that specifically cleave ubiquitin (MIM 191339) linkages, negating the action of ubiquitin ligases. DUBA7 belongs to a DUB subfamily characterized by an ovarian tumor (OTU) domain.[supplied by OMIM, May 2008]","start":23439458,"end":23442390,"strand":1,"description":"OTU deubiquitinase 1 [Source:HGNC Symbol;Acc:HGNC:27346]"}, {"versioned_ensembl_gene_id":"ENSG00000263309.6","gene_symbol":"KRT23","gene_name":"keratin 23 [Source:HGNC Symbol;Acc:HGNC:6438]","synonyms":"MGC26158,K23,HAIK1,DKFZP434G032,CK23","biotype":"protein_coding","ncbi_id":"25984","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":40922696,"end":40937634,"strand":-1,"description":"keratin 23 [Source:HGNC Symbol;Acc:HGNC:6438]"}, {"versioned_ensembl_gene_id":"ENSG00000262487.1","gene_symbol":"AC037482.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40921430,"end":40976053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092140.14","gene_symbol":"G2E3","gene_name":"G2/M-phase specific E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:20338]","synonyms":"PHF7B,KIAA1333,FLJ20333","biotype":"protein_coding","ncbi_id":"55632","summary":null,"start":30559123,"end":30620063,"strand":1,"description":"G2/M-phase specific E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:20338]"}, {"versioned_ensembl_gene_id":"ENSG00000130703.15","gene_symbol":"OSBPL2","gene_name":"oxysterol binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:15761]","synonyms":"ORP-2,KIAA0772,DFNA67","biotype":"protein_coding","ncbi_id":"9885","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although the encoded protein contains only the sterol-binding domain. In vitro studies have shown that the encoded protein can bind strongly to phosphatic acid and weakly to phosphatidylinositol 3-phosphate, but cannot bind to 25-hydroxycholesterol. The protein associates with the Golgi apparatus. Transcript variants encoding different isoforms have been described. [provided by RefSeq, Sep 2014]","start":62231922,"end":62296213,"strand":1,"description":"oxysterol binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:15761]"}, {"versioned_ensembl_gene_id":"ENSG00000226489.1","gene_symbol":"AC104308.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35871866,"end":35872198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235820.1","gene_symbol":"AL109935.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5533628,"end":5535889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227982.1","gene_symbol":"RPL7P30","gene_name":"ribosomal protein L7 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36151]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270908","summary":null,"start":84528122,"end":84528830,"strand":-1,"description":"ribosomal protein L7 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36151]"}, {"versioned_ensembl_gene_id":"ENSG00000171962.17","gene_symbol":"DRC3","gene_name":"dynein regulatory complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25384]","synonyms":"LRRC48,DKFZP586M1120,CFAP134","biotype":"protein_coding","ncbi_id":"83450","summary":null,"start":17972813,"end":18016889,"strand":1,"description":"dynein regulatory complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:25384]"}, {"versioned_ensembl_gene_id":"ENSG00000262826.5","gene_symbol":"INTS3","gene_name":"integrator complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26153]","synonyms":"SOSS-A,INT3,FLJ21919,C1orf60","biotype":"protein_coding","ncbi_id":"65123","summary":"The protein encoded by this gene can form a complex with human single-strand DNA binding proteins 1 or 2 (hSSB1 and hSSB2) and other proteins to mediate genome stability and the DNA damage response. The encoded protein is also part of a multiprotein complex that interacts with the C-terminal domain of RNA polymerase II large subunit to help regulate processing of U1 and U2 small nuclear RNAs. [provided by RefSeq, May 2016]","start":153745298,"end":153792039,"strand":1,"description":"integrator complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26153]"}, {"versioned_ensembl_gene_id":"ENSG00000111615.13","gene_symbol":"KRR1","gene_name":"KRR1, small subunit processome component homolog [Source:HGNC Symbol;Acc:HGNC:5176]","synonyms":"RIP-1,HRB2","biotype":"protein_coding","ncbi_id":"11103","summary":null,"start":75490861,"end":75511636,"strand":-1,"description":"KRR1, small subunit processome component homolog [Source:HGNC Symbol;Acc:HGNC:5176]"}, {"versioned_ensembl_gene_id":"ENSG00000159433.11","gene_symbol":"STARD9","gene_name":"StAR related lipid transfer domain containing 9 [Source:HGNC Symbol;Acc:HGNC:19162]","synonyms":"KIF16A,KIAA1300","biotype":"protein_coding","ncbi_id":"57519","summary":null,"start":42575659,"end":42720981,"strand":1,"description":"StAR related lipid transfer domain containing 9 [Source:HGNC Symbol;Acc:HGNC:19162]"}, {"versioned_ensembl_gene_id":"ENSG00000282519.1","gene_symbol":"IQANK1","gene_name":"IQ motif and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:49576]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"642574","summary":null,"start":143775927,"end":143777466,"strand":1,"description":"IQ motif and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:49576]"}, {"versioned_ensembl_gene_id":"ENSG00000225640.1","gene_symbol":"LINC01729","gene_name":"long intergenic non-protein coding RNA 1729 [Source:HGNC Symbol;Acc:HGNC:52517]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929207","summary":null,"start":5507875,"end":5510002,"strand":-1,"description":"long intergenic non-protein coding RNA 1729 [Source:HGNC Symbol;Acc:HGNC:52517]"}, {"versioned_ensembl_gene_id":"ENSG00000242299.1","gene_symbol":"AC073861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101576489,"end":101576947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259123.1","gene_symbol":"AC103996.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93837611,"end":93852981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258831.1","gene_symbol":"AC103996.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93882082,"end":93886743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229929.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30316398,"end":30333651,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000112273.6","gene_symbol":"HDGFL1","gene_name":"HDGF like 1 [Source:HGNC Symbol;Acc:HGNC:21095]","synonyms":"PWWP1,HRP-1,Hdgfrp1,dJ309H15.1","biotype":"protein_coding","ncbi_id":"154150","summary":null,"start":22569493,"end":22571666,"strand":1,"description":"HDGF like 1 [Source:HGNC Symbol;Acc:HGNC:21095]"}, {"versioned_ensembl_gene_id":"ENSG00000243008.2","gene_symbol":"AL359538.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":24566873,"end":24597676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120057.4","gene_symbol":"SFRP5","gene_name":"secreted frizzled related protein 5 [Source:HGNC Symbol;Acc:HGNC:10779]","synonyms":"SARP3","biotype":"protein_coding","ncbi_id":"6425","summary":"Secreted frizzled-related protein 5 (SFRP5) is a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins. SFRPs act as soluble modulators of Wnt signaling. SFRP5 and SFRP1 may be involved in determining the polarity of photoreceptor cells in the retina. SFRP5 is highly expressed in the retinal pigment epithelium, and moderately expressed in the pancreas. [provided by RefSeq, Jul 2008]","start":97766751,"end":97771952,"strand":-1,"description":"secreted frizzled related protein 5 [Source:HGNC Symbol;Acc:HGNC:10779]"}, {"versioned_ensembl_gene_id":"ENSG00000244615.1","gene_symbol":"PSPC1P2","gene_name":"paraspeckle component 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42643]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100873875","summary":null,"start":24566843,"end":24570728,"strand":1,"description":"paraspeckle component 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42643]"}, {"versioned_ensembl_gene_id":"ENSG00000280898.1","gene_symbol":"AC233714.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166275457,"end":166277068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065325.12","gene_symbol":"GLP2R","gene_name":"glucagon like peptide 2 receptor [Source:HGNC Symbol;Acc:HGNC:4325]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9340","summary":"This gene encodes a G protein-coupled receptor that is closely related to the glucagon receptor and binds to glucagon-like peptide-2 (GLP2). Signalling through GLP2 stimulates intestinal growth and increases villus height in the small intestine, concomitant with increased crypt cell proliferation and decreased enterocyte apoptosis. [provided by RefSeq, Dec 2014]","start":9822206,"end":9892102,"strand":1,"description":"glucagon like peptide 2 receptor [Source:HGNC Symbol;Acc:HGNC:4325]"}, {"versioned_ensembl_gene_id":"ENSG00000265593.1","gene_symbol":"NPM1P45","gene_name":"nucleophosmin 1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:45224]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422316","summary":null,"start":9852748,"end":9853306,"strand":-1,"description":"nucleophosmin 1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:45224]"}, {"versioned_ensembl_gene_id":"ENSG00000280429.1","gene_symbol":"AF001548.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15790975,"end":15792717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173612.9","gene_symbol":"GPRC6A","gene_name":"G protein-coupled receptor class C group 6 member A [Source:HGNC Symbol;Acc:HGNC:18510]","synonyms":"bA86F4.3","biotype":"protein_coding","ncbi_id":"222545","summary":"Members of family C of the G protein-coupled receptor (GPCR) superfamily, such as GPRC6A, are characterized by an evolutionarily conserved amino acid-sensing motif linked to an intramembranous 7-transmembrane loop region. Several members of GPCR family C, including GPRC6A, also have a long N-terminal domain (summary by Pi et al., 2005 [PubMed 16199532]).[supplied by OMIM, Nov 2010]","start":116792085,"end":116829037,"strand":-1,"description":"G protein-coupled receptor class C group 6 member A [Source:HGNC Symbol;Acc:HGNC:18510]"}, {"versioned_ensembl_gene_id":"ENSG00000282725.1","gene_symbol":"CORO7","gene_name":"coronin 7 [Source:HGNC Symbol;Acc:HGNC:26161]","synonyms":"FLJ22021","biotype":"protein_coding","ncbi_id":"79585","summary":"This gene encodes a member of the coronin protein family. However, unlike other coronin proteins, it is not an actin-binding protein but rather functions as an F-actin regulator directing anterograde Golgi to endosome transport. The encoded protein has two tandem WD-40 domain repeats and localizes to the trans-Golgi network. The protein undergoes K33-linked polyubiquitination via an E3 ligase complex. It is thought to play an essential role in maintenance of Golgi apparatus morphology. Alternative splicing results in multiple transcripts variants; some of which form read-through transcripts with a neighboring gene. [provided by RefSeq, Dec 2016]","start":4356503,"end":4427664,"strand":-1,"description":"coronin 7 [Source:HGNC Symbol;Acc:HGNC:26161]"}, {"versioned_ensembl_gene_id":"ENSG00000260490.2","gene_symbol":"MYL12BP1","gene_name":"myosin light chain 12B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645094","summary":null,"start":42571927,"end":42572433,"strand":1,"description":"myosin light chain 12B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51649]"}, {"versioned_ensembl_gene_id":"ENSG00000100997.18","gene_symbol":"ABHD12","gene_name":"abhydrolase domain containing 12 [Source:HGNC Symbol;Acc:HGNC:15868]","synonyms":"DKFZP434P106,dJ965G21.2,C20orf22,BEM46L2,ABHD12A","biotype":"protein_coding","ncbi_id":"26090","summary":"This gene encodes an enzyme that catalyzes the hydrolysis of 2-arachidonoyl glycerol (2-AG), the main endocannabinoid lipid transmitter that acts on cannabinoid receptors, CB1 and CB2. The endocannabinoid system is involved in a wide range of physiological processes, including neurotransmission, mood, appetite, pain appreciation, addiction behavior, and inflammation. Mutations in this gene are associated with the neurodegenerative disease, PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract), resulting from an inborn error of endocannabinoid metabolism. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jan 2011]","start":25294743,"end":25390983,"strand":-1,"description":"abhydrolase domain containing 12 [Source:HGNC Symbol;Acc:HGNC:15868]"}, {"versioned_ensembl_gene_id":"ENSG00000227907.1","gene_symbol":"AL158837.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167052551,"end":167058542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255996.1","gene_symbol":"AC005906.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5032388,"end":5032941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282011.1","gene_symbol":"AC004789.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4348654,"end":4350608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170777.10","gene_symbol":"TPD52L3","gene_name":"tumor protein D52 like 3 [Source:HGNC Symbol;Acc:HGNC:23382]","synonyms":"NYD-SP25","biotype":"protein_coding","ncbi_id":"89882","summary":"This gene encodes a member of the tumor protein D52-like family of proteins. These proteins are characterized by an N-terminal coiled-coil motif that is used to form homo- and heteromeric complexes with other tumor protein D52-like proteins. The encoded protein may play a role in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":6328375,"end":6331900,"strand":1,"description":"tumor protein D52 like 3 [Source:HGNC Symbol;Acc:HGNC:23382]"}, {"versioned_ensembl_gene_id":"ENSG00000124103.8","gene_symbol":"FAM209A","gene_name":"family with sequence similarity 209 member A [Source:HGNC Symbol;Acc:HGNC:16100]","synonyms":"dJ1153D9.3,C20orf106","biotype":"protein_coding","ncbi_id":"200232","summary":null,"start":56517187,"end":56526142,"strand":1,"description":"family with sequence similarity 209 member A [Source:HGNC Symbol;Acc:HGNC:16100]"}, {"versioned_ensembl_gene_id":"ENSG00000204564.11","gene_symbol":"C6orf136","gene_name":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]","synonyms":"Em:AB023049.8","biotype":"protein_coding","ncbi_id":"221545","summary":null,"start":30647039,"end":30653210,"strand":1,"description":"chromosome 6 open reading frame 136 [Source:HGNC Symbol;Acc:HGNC:21301]"}, {"versioned_ensembl_gene_id":"ENSG00000278760.4","gene_symbol":"CORO7-PAM16","gene_name":"CORO7-PAM16 readthrough [Source:HGNC Symbol;Acc:HGNC:44424]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529144","summary":"This locus represents naturally occurring read-through transcription between the neighboring CORO7 (coronin 7) and PAM16 (presequence translocase-associated motor 16) genes on chromosome 16. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jan 2011]","start":4340251,"end":4422453,"strand":-1,"description":"CORO7-PAM16 readthrough [Source:HGNC Symbol;Acc:HGNC:44424]"}, {"versioned_ensembl_gene_id":"ENSG00000106245.10","gene_symbol":"BUD31","gene_name":"BUD31 homolog [Source:HGNC Symbol;Acc:HGNC:29629]","synonyms":"YCR063W,G10,fSAP17,EDG2,EDG-2,Cwc14","biotype":"protein_coding","ncbi_id":"8896","summary":null,"start":99408641,"end":99419616,"strand":1,"description":"BUD31 homolog [Source:HGNC Symbol;Acc:HGNC:29629]"}, {"versioned_ensembl_gene_id":"ENSG00000236797.1","gene_symbol":"SPA17P1","gene_name":"sperm autoantigenic protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23224]","synonyms":"Sp17-2","biotype":"transcribed_processed_pseudogene","ncbi_id":"171424","summary":null,"start":75382393,"end":75382844,"strand":-1,"description":"sperm autoantigenic protein 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23224]"}, {"versioned_ensembl_gene_id":"ENSG00000127483.17","gene_symbol":"HP1BP3","gene_name":"heterochromatin protein 1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:24973]","synonyms":"HP1-BP74","biotype":"protein_coding","ncbi_id":"50809","summary":null,"start":20742661,"end":20787323,"strand":-1,"description":"heterochromatin protein 1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:24973]"}, {"versioned_ensembl_gene_id":"ENSG00000258888.1","gene_symbol":"AC112693.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93257198,"end":93260475,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104140.6","gene_symbol":"RHOV","gene_name":"ras homolog family member V [Source:HGNC Symbol;Acc:HGNC:18313]","synonyms":"WRCH2,Chp,ARHV","biotype":"protein_coding","ncbi_id":"171177","summary":null,"start":40872214,"end":40874289,"strand":-1,"description":"ras homolog family member V [Source:HGNC Symbol;Acc:HGNC:18313]"}, {"versioned_ensembl_gene_id":"ENSG00000254275.6","gene_symbol":"LINC00824","gene_name":"long intergenic non-protein coding RNA 824 [Source:HGNC Symbol;Acc:HGNC:50281]","synonyms":"LINC01263","biotype":"processed_transcript","ncbi_id":"101927774","summary":null,"start":128405269,"end":128564679,"strand":-1,"description":"long intergenic non-protein coding RNA 824 [Source:HGNC Symbol;Acc:HGNC:50281]"}, {"versioned_ensembl_gene_id":"ENSG00000223428.1","gene_symbol":"AC010997.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":75288333,"end":75288682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280076.1","gene_symbol":"AC112693.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93206066,"end":93208048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268149.1","gene_symbol":"AC010336.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7912648,"end":7913518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277140.2","gene_symbol":"MARF1","gene_name":"meiosis regulator and mRNA stability factor 1 [Source:HGNC Symbol;Acc:HGNC:29562]","synonyms":"LMKB,LKAP,KIAA0430,PPP1R34,Marf1","biotype":"protein_coding","ncbi_id":"9665","summary":"This gene encodes a putative peroxisomal protein that appears to be conserved across Euteleostomi. In humans, it may be autoantigenic. [provided by RefSeq, Jul 2010]","start":15679520,"end":15728320,"strand":-1,"description":"meiosis regulator and mRNA stability factor 1 [Source:HGNC Symbol;Acc:HGNC:29562]"}, {"versioned_ensembl_gene_id":"ENSG00000025770.18","gene_symbol":"NCAPH2","gene_name":"non-SMC condensin II complex subunit H2 [Source:HGNC Symbol;Acc:HGNC:25071]","synonyms":"hCAP-H2,CAP-H2,384D8-2","biotype":"protein_coding","ncbi_id":"29781","summary":"This gene encodes one of the non-SMC subunits of the condensin II complex. This complex plays an essential role in mitotic chromosome assembly. Alternate splicing of this gene results in multiple transcript variants.[provided by RefSeq, May 2010]","start":50508216,"end":50523472,"strand":1,"description":"non-SMC condensin II complex subunit H2 [Source:HGNC Symbol;Acc:HGNC:25071]"}, {"versioned_ensembl_gene_id":"ENSG00000204006.8","gene_symbol":"C1orf185","gene_name":"chromosome 1 open reading frame 185 [Source:HGNC Symbol;Acc:HGNC:28096]","synonyms":"FLJ27485","biotype":"protein_coding","ncbi_id":"284546","summary":null,"start":51102234,"end":51148086,"strand":1,"description":"chromosome 1 open reading frame 185 [Source:HGNC Symbol;Acc:HGNC:28096]"}, {"versioned_ensembl_gene_id":"ENSG00000238166.2","gene_symbol":"AC022748.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":78752107,"end":78753373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231822.1","gene_symbol":"AC019097.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99102018,"end":99102752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257392.1","gene_symbol":"AC126177.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":107887730,"end":107889886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257951.2","gene_symbol":"AC126177.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":107880581,"end":107883386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147421.17","gene_symbol":"HMBOX1","gene_name":"homeobox containing 1 [Source:HGNC Symbol;Acc:HGNC:26137]","synonyms":"PBHNF,HOT1,HNF1LA,FLJ21616","biotype":"protein_coding","ncbi_id":"79618","summary":null,"start":28890394,"end":29064764,"strand":1,"description":"homeobox containing 1 [Source:HGNC Symbol;Acc:HGNC:26137]"}, {"versioned_ensembl_gene_id":"ENSG00000164989.16","gene_symbol":"CCDC171","gene_name":"coiled-coil domain containing 171 [Source:HGNC Symbol;Acc:HGNC:29828]","synonyms":"Em:AL513423.1,C9orf93,bA778P13.1,bA536D16.1,FLJ46740,FLJ39267","biotype":"protein_coding","ncbi_id":"203238","summary":null,"start":15553086,"end":16061663,"strand":1,"description":"coiled-coil domain containing 171 [Source:HGNC Symbol;Acc:HGNC:29828]"}, {"versioned_ensembl_gene_id":"ENSG00000277324.1","gene_symbol":"AC093462.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54268346,"end":54270028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203781.4","gene_symbol":"AL591704.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153427020,"end":153428401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254530.1","gene_symbol":"AC090124.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29335878,"end":29594295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255227.1","gene_symbol":"AC090124.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29445487,"end":29457393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255281.1","gene_symbol":"AC090124.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29391525,"end":29393844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255029.1","gene_symbol":"AC110058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29519076,"end":29552639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197872.11","gene_symbol":"FAM49A","gene_name":"family with sequence similarity 49 member A [Source:HGNC Symbol;Acc:HGNC:25373]","synonyms":"FLJ11080,DKFZP566A1524","biotype":"protein_coding","ncbi_id":"81553","summary":null,"start":16549459,"end":16666331,"strand":-1,"description":"family with sequence similarity 49 member A [Source:HGNC Symbol;Acc:HGNC:25373]"}, {"versioned_ensembl_gene_id":"ENSG00000258018.1","gene_symbol":"LINC02457","gene_name":"long intergenic non-protein coding RNA 2457 [Source:HGNC Symbol;Acc:HGNC:53393]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984439","summary":null,"start":116517858,"end":116518820,"strand":1,"description":"long intergenic non-protein coding RNA 2457 [Source:HGNC Symbol;Acc:HGNC:53393]"}, {"versioned_ensembl_gene_id":"ENSG00000271523.1","gene_symbol":"AL049634.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1591392,"end":1591848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258346.1","gene_symbol":"AC079384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116368764,"end":116389471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205126.2","gene_symbol":"ACCSL","gene_name":"1-aminocyclopropane-1-carboxylate synthase homolog (inactive) like [Source:HGNC Symbol;Acc:HGNC:34391]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390110","summary":null,"start":44047981,"end":44059977,"strand":1,"description":"1-aminocyclopropane-1-carboxylate synthase homolog (inactive) like [Source:HGNC Symbol;Acc:HGNC:34391]"}, {"versioned_ensembl_gene_id":"ENSG00000249867.5","gene_symbol":"AC090833.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28702615,"end":29063821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073146.15","gene_symbol":"MOV10L1","gene_name":"Mov10 RISC complex RNA helicase like 1 [Source:HGNC Symbol;Acc:HGNC:7201]","synonyms":"DKFZp434B0717,DJ402G11.8,CHAMP","biotype":"protein_coding","ncbi_id":"54456","summary":"This gene is similar to a mouse gene that encodes a putative RNA helicase and shows testis-specific expression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":50089879,"end":50161690,"strand":1,"description":"Mov10 RISC complex RNA helicase like 1 [Source:HGNC Symbol;Acc:HGNC:7201]"}, {"versioned_ensembl_gene_id":"ENSG00000106244.12","gene_symbol":"PDAP1","gene_name":"PDGFA associated protein 1 [Source:HGNC Symbol;Acc:HGNC:14634]","synonyms":"PAP1,PAP,HASPP28","biotype":"protein_coding","ncbi_id":"11333","summary":"The protein encoded by this gene is a phosphoprotein that may upregulate the PDGFA-stimulated growth of fibroblasts and also downregulate the mitogenicity of PDGFB. The encoded protein in rodents has been shown to bind PDGFA with a low affinity. [provided by RefSeq, Dec 2010]","start":99392048,"end":99408829,"strand":-1,"description":"PDGFA associated protein 1 [Source:HGNC Symbol;Acc:HGNC:14634]"}, {"versioned_ensembl_gene_id":"ENSG00000065060.16","gene_symbol":"UHRF1BP1","gene_name":"UHRF1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21216]","synonyms":"ICBP90,FLJ20302,dJ349A12.1,C6orf107","biotype":"protein_coding","ncbi_id":"54887","summary":null,"start":34792015,"end":34883138,"strand":1,"description":"UHRF1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:21216]"}, {"versioned_ensembl_gene_id":"ENSG00000267541.1","gene_symbol":"MTCO2P2","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:25354]","synonyms":"HsT4010","biotype":"processed_pseudogene","ncbi_id":"100873202","summary":null,"start":47853233,"end":47853457,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:25354]"}, {"versioned_ensembl_gene_id":"ENSG00000269365.2","gene_symbol":"AC120349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47878295,"end":47882444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182175.13","gene_symbol":"RGMA","gene_name":"repulsive guidance molecule family member a [Source:HGNC Symbol;Acc:HGNC:30308]","synonyms":"RGMa,RGM","biotype":"protein_coding","ncbi_id":"56963","summary":"This gene encodes a member of the repulsive guidance molecule family. The encoded protein is a glycosylphosphatidylinositol-anchored glycoprotein that functions as an axon guidance protein in the developing and adult central nervous system. This protein may also function as a tumor suppressor in some cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":93035273,"end":93089204,"strand":-1,"description":"repulsive guidance molecule family member a [Source:HGNC Symbol;Acc:HGNC:30308]"}, {"versioned_ensembl_gene_id":"ENSG00000204410.14","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31739948,"end":31762834,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000171566.11","gene_symbol":"PLRG1","gene_name":"pleiotropic regulator 1 [Source:HGNC Symbol;Acc:HGNC:9089]","synonyms":"TANGO4,PRPF46,Prp46,PRL1,Cwc1","biotype":"protein_coding","ncbi_id":"5356","summary":"This gene encodes a core component of the cell division cycle 5-like (CDC5L) complex. The CDC5L complex is part of the spliceosome and is required for pre-mRNA splicing. The encoded protein plays a critical role in alternative splice site selection. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":154535006,"end":154550435,"strand":-1,"description":"pleiotropic regulator 1 [Source:HGNC Symbol;Acc:HGNC:9089]"}, {"versioned_ensembl_gene_id":"ENSG00000273096.1","gene_symbol":"AL021707.8","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38736610,"end":38736792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259277.1","gene_symbol":"AC127522.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28970196,"end":28977464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253631.1","gene_symbol":"IGLV7-35","gene_name":"immunoglobulin lambda variable 7-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5928]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28777","summary":null,"start":22450202,"end":22450652,"strand":1,"description":"immunoglobulin lambda variable 7-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5928]"}, {"versioned_ensembl_gene_id":"ENSG00000234046.7","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30174807,"end":30203783,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000278916.1","gene_symbol":"CEP83-AS1","gene_name":"CEP83 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27055]","synonyms":"CCDC41-AS1","biotype":"lincRNA","ncbi_id":"144486","summary":null,"start":94460003,"end":94462484,"strand":1,"description":"CEP83 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27055]"}, {"versioned_ensembl_gene_id":"ENSG00000146463.11","gene_symbol":"ZMYM4","gene_name":"zinc finger MYM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:13055]","synonyms":"ZNF262,ZNF198L3,MYM,KIAA0425","biotype":"protein_coding","ncbi_id":"9202","summary":null,"start":35268967,"end":35422058,"strand":1,"description":"zinc finger MYM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:13055]"}, {"versioned_ensembl_gene_id":"ENSG00000273115.1","gene_symbol":"AP001596.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26459903,"end":26460214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166265.11","gene_symbol":"CYYR1","gene_name":"cysteine and tyrosine rich 1 [Source:HGNC Symbol;Acc:HGNC:16274]","synonyms":"C21orf95","biotype":"protein_coding","ncbi_id":"116159","summary":null,"start":26466209,"end":26573284,"strand":-1,"description":"cysteine and tyrosine rich 1 [Source:HGNC Symbol;Acc:HGNC:16274]"}, {"versioned_ensembl_gene_id":"ENSG00000065978.18","gene_symbol":"YBX1","gene_name":"Y-box binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8014]","synonyms":"NSEP1,NSEP-1,MDR-NF1,DBPB,CSDB,CSDA2,BP-8,YB1,YB-1","biotype":"protein_coding","ncbi_id":"4904","summary":"This gene encodes a highly conserved cold shock domain protein that has broad nucleic acid binding properties. The encoded protein functions as both a DNA and RNA binding protein and has been implicated in numerous cellular processes including regulation of transcription and translation, pre-mRNA splicing, DNA reparation and mRNA packaging. This protein is also a component of messenger ribonucleoprotein (mRNP) complexes and may have a role in microRNA processing. This protein can be secreted through non-classical pathways and functions as an extracellular mitogen. Aberrant expression of the gene is associated with cancer proliferation in numerous tissues. This gene may be a prognostic marker for poor outcome and drug resistance in certain cancers. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on multiple chromosomes. [provided by RefSeq, Sep 2015]","start":42682427,"end":42702349,"strand":1,"description":"Y-box binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8014]"}, {"versioned_ensembl_gene_id":"ENSG00000229025.1","gene_symbol":"AP001595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26349780,"end":26350634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130943.6","gene_symbol":"PKDREJ","gene_name":"polycystin family receptor for egg jelly [Source:HGNC Symbol;Acc:HGNC:9015]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10343","summary":"This intronless gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a receptor for egg jelly (REJ) domain, a G-protein-coupled receptor proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may play a role in human reproduction. Alternative splice variants have been described but their biological natures have not been determined. [provided by RefSeq, Jul 2008]","start":46255663,"end":46263355,"strand":-1,"description":"polycystin family receptor for egg jelly [Source:HGNC Symbol;Acc:HGNC:9015]"}, {"versioned_ensembl_gene_id":"ENSG00000144959.9","gene_symbol":"NCEH1","gene_name":"neutral cholesterol ester hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:29260]","synonyms":"NCEH,KIAA1363,AADACL1","biotype":"protein_coding","ncbi_id":"57552","summary":null,"start":172630249,"end":172711218,"strand":-1,"description":"neutral cholesterol ester hydrolase 1 [Source:HGNC Symbol;Acc:HGNC:29260]"}, {"versioned_ensembl_gene_id":"ENSG00000268069.2","gene_symbol":"AC004466.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47784923,"end":47786002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231384.1","gene_symbol":"AC007919.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172680714,"end":172681224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235756.2","gene_symbol":"AC098657.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80092103,"end":80093237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228212.1","gene_symbol":"OFD1P17","gene_name":"OFD1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:1332]","synonyms":"OFD1P1,C5orf1,71-7A5,71-7A3","biotype":"processed_pseudogene","ncbi_id":"23738","summary":null,"start":37209364,"end":37212381,"strand":1,"description":"OFD1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:1332]"}, {"versioned_ensembl_gene_id":"ENSG00000214210.4","gene_symbol":"AC084017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":164001606,"end":164002465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136541.14","gene_symbol":"ERMN","gene_name":"ermin [Source:HGNC Symbol;Acc:HGNC:29208]","synonyms":"KIAA1189,JN,ERMIN","biotype":"protein_coding","ncbi_id":"57471","summary":null,"start":157318625,"end":157327713,"strand":-1,"description":"ermin [Source:HGNC Symbol;Acc:HGNC:29208]"}, {"versioned_ensembl_gene_id":"ENSG00000227972.1","gene_symbol":"THAP12P3","gene_name":"THAP domain containing 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39567]","synonyms":"PRKRIRP3","biotype":"processed_pseudogene","ncbi_id":"399774","summary":null,"start":52411135,"end":52413492,"strand":1,"description":"THAP domain containing 12 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39567]"}, {"versioned_ensembl_gene_id":"ENSG00000226348.1","gene_symbol":"VN2R10P","gene_name":"vomeronasal 2 receptor 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:33216]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100033398","summary":null,"start":77220406,"end":77221258,"strand":1,"description":"vomeronasal 2 receptor 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:33216]"}, {"versioned_ensembl_gene_id":"ENSG00000258028.1","gene_symbol":"AL138974.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28936889,"end":29028763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163848.19","gene_symbol":"ZNF148","gene_name":"zinc finger protein 148 [Source:HGNC Symbol;Acc:HGNC:12933]","synonyms":"ZFP148,ZBP-89,pHZ-52,HT-BETA,BFCOL1,BERF-1","biotype":"protein_coding","ncbi_id":"7707","summary":"The protein encoded by this gene is a member of the Kruppel family of zinc finger DNA binding proteins. The encoded protein activates transcription of the T-cell receptor and intestinal alkaline phosphatase genes but represses transcription of the ornithine decarboxylase, vimentin, gastrin, stomelysin, and enolase genes. Increased expression of this gene results in decreased patient survival rates from colorectal cancer, while mutations in this gene have been associated with global developmental delay, hypoplastic corpus callosum, and dysmorphic facies. [provided by RefSeq, Feb 2017]","start":125225561,"end":125375354,"strand":-1,"description":"zinc finger protein 148 [Source:HGNC Symbol;Acc:HGNC:12933]"}, {"versioned_ensembl_gene_id":"ENSG00000260417.1","gene_symbol":"AC092127.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85592266,"end":85595720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231991.4","gene_symbol":"ANXA2P2","gene_name":"annexin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:539]","synonyms":"ANX2L2,LPC2B,ANX2P2","biotype":"processed_pseudogene","ncbi_id":"304","summary":null,"start":33624274,"end":33625293,"strand":1,"description":"annexin A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:539]"}, {"versioned_ensembl_gene_id":"ENSG00000159753.13","gene_symbol":"CARMIL2","gene_name":"capping protein regulator and myosin 1 linker 2 [Source:HGNC Symbol;Acc:HGNC:27089]","synonyms":"RLTPR,LRRC16C","biotype":"protein_coding","ncbi_id":"146206","summary":"This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017]","start":67644919,"end":67657569,"strand":1,"description":"capping protein regulator and myosin 1 linker 2 [Source:HGNC Symbol;Acc:HGNC:27089]"}, {"versioned_ensembl_gene_id":"ENSG00000114923.16","gene_symbol":"SLC4A3","gene_name":"solute carrier family 4 member 3 [Source:HGNC Symbol;Acc:HGNC:11029]","synonyms":"SLC2C,AE3","biotype":"protein_coding","ncbi_id":"6508","summary":"The protein encoded by this gene is a plasma membrane anion exchange protein. The encoded protein has been found in brain, heart, kidney, small intestine, and lung. [provided by RefSeq, May 2016]","start":219627327,"end":219641980,"strand":1,"description":"solute carrier family 4 member 3 [Source:HGNC Symbol;Acc:HGNC:11029]"}, {"versioned_ensembl_gene_id":"ENSG00000189067.12","gene_symbol":"LITAF","gene_name":"lipopolysaccharide induced TNF factor [Source:HGNC Symbol;Acc:HGNC:16841]","synonyms":"TP53I7,SIMPLE,PIG7,FLJ38636","biotype":"protein_coding","ncbi_id":"9516","summary":"Lipopolysaccharide is a potent stimulator of monocytes and macrophages, causing secretion of tumor necrosis factor-alpha (TNF-alpha) and other inflammatory mediators. This gene encodes lipopolysaccharide-induced TNF-alpha factor, which is a DNA-binding protein and can mediate the TNF-alpha expression by direct binding to the promoter region of the TNF-alpha gene. The transcription of this gene is induced by tumor suppressor p53 and has been implicated in the p53-induced apoptotic pathway. Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014]","start":11547722,"end":11636381,"strand":-1,"description":"lipopolysaccharide induced TNF factor [Source:HGNC Symbol;Acc:HGNC:16841]"}, {"versioned_ensembl_gene_id":"ENSG00000241169.1","gene_symbol":"FO393419.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27457198,"end":27459582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231444.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bPG70P20.2,TIGD1L,bCX111D4.7,bQB10J12.1","biotype":"processed_transcript","ncbi_id":"414771","summary":null,"start":30911634,"end":30920567,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000272168.6","gene_symbol":"CASC15","gene_name":"cancer susceptibility 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:28245]","synonyms":"lnc-SOX4-1,LINC00340","biotype":"lincRNA","ncbi_id":"401237","summary":"This gene produces a long non-coding RNA that may regulate cell proliferation. This RNA is upregulated in hepatocellular carcinoma, where it is thought to function as an oncogene. However, some splice variants of this gene may function as a tumor suppressor in neuroblastoma and other tumor types. Circular RNA variants were observed at this gene. [provided by RefSeq, Dec 2017]","start":21664772,"end":22368328,"strand":1,"description":"cancer susceptibility 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:28245]"}, {"versioned_ensembl_gene_id":"ENSG00000213983.11","gene_symbol":"AP1G2","gene_name":"adaptor related protein complex 1 gamma 2 subunit [Source:HGNC Symbol;Acc:HGNC:556]","synonyms":"G2AD","biotype":"protein_coding","ncbi_id":"8906","summary":"Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes. The adaptin family of proteins is composed of four classes of molecules named alpha, beta-, beta prime- and gamma- adaptins. Adaptins, together with medium and small subunits, form a heterotetrameric complex called an adaptor, whose role is to promote the formation of clathrin-coated pits and vesicles. The protein encoded by this gene is a gamma-adaptin protein and it belongs to the adaptor complexes large subunits family. This protein along with the complex is thought to function at some trafficking step in the complex pathways between the trans-Golgi network and the cell surface. [provided by RefSeq, Aug 2017]","start":23559565,"end":23568070,"strand":-1,"description":"adaptor related protein complex 1 gamma 2 subunit [Source:HGNC Symbol;Acc:HGNC:556]"}, {"versioned_ensembl_gene_id":"ENSG00000090905.18","gene_symbol":"TNRC6A","gene_name":"trinucleotide repeat containing 6A [Source:HGNC Symbol;Acc:HGNC:11969]","synonyms":"TNRC6,KIAA1460,GW182,CAGH26","biotype":"protein_coding","ncbi_id":"27327","summary":"This gene encodes a member of the trinucleotide repeat containing 6 protein family. The protein functions in post-transcriptional gene silencing through the RNA interference (RNAi) and microRNA pathways. The protein associates with messenger RNAs and Argonaute proteins in cytoplasmic bodies known as GW-bodies or P-bodies. Inhibiting expression of this gene delocalizes other GW-body proteins and impairs RNAi and microRNA-induced gene silencing. [provided by RefSeq, Jul 2008]","start":24610209,"end":24827632,"strand":1,"description":"trinucleotide repeat containing 6A [Source:HGNC Symbol;Acc:HGNC:11969]"}, {"versioned_ensembl_gene_id":"ENSG00000214604.3","gene_symbol":"NPM1P36","gene_name":"nucleophosmin 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45215]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652423","summary":null,"start":55939790,"end":55940624,"strand":-1,"description":"nucleophosmin 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:45215]"}, {"versioned_ensembl_gene_id":"ENSG00000267544.1","gene_symbol":"AC007229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10841839,"end":10842250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203785.8","gene_symbol":"SPRR2E","gene_name":"small proline rich protein 2E [Source:HGNC Symbol;Acc:HGNC:11265]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6704","summary":"This gene encodes a member of a family of small proline-rich proteins clustered in the epidermal differentiation complex on chromosome 1q21. The encoded protein, along with other family members, is a component of the cornified cell envelope that forms beneath the plasma membrane in terminally differentiated stratified squamous epithelia. This envelope serves as a barrier against extracellular and environmental factors. The seven SPRR2 genes (A-G) appear to have been homogenized by gene conversion compared to others in the cluster that exhibit greater differences in protein structure. [provided by RefSeq, Feb 2014]","start":153093135,"end":153106184,"strand":-1,"description":"small proline rich protein 2E [Source:HGNC Symbol;Acc:HGNC:11265]"}, {"versioned_ensembl_gene_id":"ENSG00000255094.1","gene_symbol":"AC090159.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27978669,"end":28019575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217315.1","gene_symbol":"OR2W2P","gene_name":"olfactory receptor family 2 subfamily W member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:13970]","synonyms":"hs6M1-30P","biotype":"unprocessed_pseudogene","ncbi_id":"81694","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":28033947,"end":28034855,"strand":1,"description":"olfactory receptor family 2 subfamily W member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:13970]"}, {"versioned_ensembl_gene_id":"ENSG00000196821.9","gene_symbol":"C6orf106","gene_name":"chromosome 6 open reading frame 106 [Source:HGNC Symbol;Acc:HGNC:21215]","synonyms":"FLJ22195,dJ391O22.4","biotype":"protein_coding","ncbi_id":"64771","summary":null,"start":34587288,"end":34696859,"strand":-1,"description":"chromosome 6 open reading frame 106 [Source:HGNC Symbol;Acc:HGNC:21215]"}, {"versioned_ensembl_gene_id":"ENSG00000232600.3","gene_symbol":"TONSL-AS1","gene_name":"TONSL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51556]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100287098","summary":null,"start":144437675,"end":144439971,"strand":1,"description":"TONSL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51556]"}, {"versioned_ensembl_gene_id":"ENSG00000173157.16","gene_symbol":"ADAMTS20","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 20 [Source:HGNC Symbol;Acc:HGNC:17178]","synonyms":"GON-1","biotype":"protein_coding","ncbi_id":"80070","summary":"The protein encoded by this gene is a member of the ADAMTS family of zinc-dependent proteases. The encoded protein has a signal peptide that is cleaved to release the mature peptide, which is secreted and found in the extracellular matrix. This protein may be involved in tissue remodeling. [provided by RefSeq, Sep 2011]","start":43353866,"end":43551921,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 20 [Source:HGNC Symbol;Acc:HGNC:17178]"}, {"versioned_ensembl_gene_id":"ENSG00000272079.2","gene_symbol":"AC004233.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3006120,"end":3007388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164889.13","gene_symbol":"SLC4A2","gene_name":"solute carrier family 4 member 2 [Source:HGNC Symbol;Acc:HGNC:11028]","synonyms":"NBND3,HKB3,EPB3L1,BND3L,AE2","biotype":"protein_coding","ncbi_id":"6522","summary":"This gene encodes a member of the anion exchanger family of membrane transport proteins. The encoded protein regulates intracellular pH, biliary bicarbonate secretion, and chloride uptake. Reduced expression of this gene may be associated with primary biliary cirrhosis (PBC) in human patients, while differential expression of this gene may be associated with malignant hepatocellular carcinoma, colon and gastric cancers. [provided by RefSeq, Nov 2016]","start":151057210,"end":151076527,"strand":1,"description":"solute carrier family 4 member 2 [Source:HGNC Symbol;Acc:HGNC:11028]"}, {"versioned_ensembl_gene_id":"ENSG00000257748.1","gene_symbol":"LINC02281","gene_name":"long intergenic non-protein coding RNA 2281 [Source:HGNC Symbol;Acc:HGNC:53197]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370423","summary":null,"start":28800084,"end":28830204,"strand":-1,"description":"long intergenic non-protein coding RNA 2281 [Source:HGNC Symbol;Acc:HGNC:53197]"}, {"versioned_ensembl_gene_id":"ENSG00000230128.3","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30787857,"end":30789212,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000175730.8","gene_symbol":"BAK1P1","gene_name":"BCL2 antagonist/killer 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:996]","synonyms":"BCL2L7P1,BAK2","biotype":"processed_pseudogene","ncbi_id":"600","summary":null,"start":32690180,"end":32690815,"strand":-1,"description":"BCL2 antagonist/killer 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:996]"}, {"versioned_ensembl_gene_id":"ENSG00000272568.5","gene_symbol":"AC005162.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28979967,"end":29013367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239697.10","gene_symbol":"TNFSF12","gene_name":"TNF superfamily member 12 [Source:HGNC Symbol;Acc:HGNC:11927]","synonyms":"APO3L,TWEAK,DR3LG","biotype":"protein_coding","ncbi_id":"8742","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein is a ligand for the FN14/TWEAKR receptor. This cytokine has overlapping signaling functions with TNF, but displays a much wider tissue distribution. This cytokine, which exists in both membrane-bound and secreted forms, can induce apoptosis via multiple pathways of cell death in a cell type-specific manner. This cytokine is also found to promote proliferation and migration of endothelial cells, and thus acts as a regulator of angiogenesis. Alternative splicing results in multiple transcript variants. Some transcripts skip the last exon of this gene and continue into the second exon of the neighboring TNFSF13 gene; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010]","start":7548891,"end":7557890,"strand":1,"description":"TNF superfamily member 12 [Source:HGNC Symbol;Acc:HGNC:11927]"}, {"versioned_ensembl_gene_id":"ENSG00000136045.11","gene_symbol":"PWP1","gene_name":"PWP1 homolog, endonuclein [Source:HGNC Symbol;Acc:HGNC:17015]","synonyms":"IEF-SSP-9502","biotype":"protein_coding","ncbi_id":"11137","summary":"The protein encoded by this gene contains several WD-40 repeats and is found mostly in the nucleus. The expression and localization of this protein are cell cycle dependent. Expression of this gene is upregulated in pancreatic adenocarcinoma. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":107685732,"end":107713167,"strand":1,"description":"PWP1 homolog, endonuclein [Source:HGNC Symbol;Acc:HGNC:17015]"}, {"versioned_ensembl_gene_id":"ENSG00000225559.1","gene_symbol":"AC083867.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138163440,"end":138164637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211651.3","gene_symbol":"IGLV1-44","gene_name":"immunoglobulin lambda variable 1-44 [Source:HGNC Symbol;Acc:HGNC:5879]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28823","summary":null,"start":22380766,"end":22381347,"strand":1,"description":"immunoglobulin lambda variable 1-44 [Source:HGNC Symbol;Acc:HGNC:5879]"}, {"versioned_ensembl_gene_id":"ENSG00000180015.12","gene_symbol":"AC093909.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188738373,"end":188739494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227562.1","gene_symbol":"AC074257.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151950386,"end":151954985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262999.1","gene_symbol":"AC099489.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11465260,"end":11473174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053918.15","gene_symbol":"KCNQ1","gene_name":"potassium voltage-gated channel subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:6294]","synonyms":"KCNA9,KCNA8,LQT1,JLNS1,LQT,KVLQT1,Kv7.1","biotype":"protein_coding","ncbi_id":"3784","summary":"This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":2444684,"end":2849109,"strand":1,"description":"potassium voltage-gated channel subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:6294]"}, {"versioned_ensembl_gene_id":"ENSG00000196593.9","gene_symbol":"ANKRD20A19P","gene_name":"ankyrin repeat domain 20 family member A19, pseudogene [Source:HGNC Symbol;Acc:HGNC:42737]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400110","summary":null,"start":23939557,"end":23946782,"strand":-1,"description":"ankyrin repeat domain 20 family member A19, pseudogene [Source:HGNC Symbol;Acc:HGNC:42737]"}, {"versioned_ensembl_gene_id":"ENSG00000280320.1","gene_symbol":"AC025262.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":64696191,"end":64696550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221882.3","gene_symbol":"OR3A2","gene_name":"olfactory receptor family 3 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8283]","synonyms":"OR228,OR17-228,OLFRA04","biotype":"protein_coding","ncbi_id":"4995","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3276942,"end":3386317,"strand":-1,"description":"olfactory receptor family 3 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8283]"}, {"versioned_ensembl_gene_id":"ENSG00000225195.2","gene_symbol":"AC078962.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":64628344,"end":64629976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274879.1","gene_symbol":"AC009804.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114929757,"end":114929935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237297.1","gene_symbol":"AL713922.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44712,"end":46884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226952.1","gene_symbol":"AC093019.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100099239,"end":100099490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262767.1","gene_symbol":"GEMIN2P1","gene_name":"gem nuclear organelle associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929669","summary":null,"start":153713833,"end":153714877,"strand":-1,"description":"gem nuclear organelle associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49561]"}, {"versioned_ensembl_gene_id":"ENSG00000156273.15","gene_symbol":"BACH1","gene_name":"BTB domain and CNC homolog 1 [Source:HGNC Symbol;Acc:HGNC:935]","synonyms":"BTBD24,BACH-1","biotype":"protein_coding","ncbi_id":"571","summary":"This gene encodes a transcription factor that belongs to the cap'n'collar type of basic region leucine zipper factor family (CNC-bZip). The encoded protein contains broad complex, tramtrack, bric-a-brac/poxvirus and zinc finger (BTB/POZ) domains, which is atypical of CNC-bZip family members. These BTB/POZ domains facilitate protein-protein interactions and formation of homo- and/or hetero-oligomers. When this encoded protein forms a heterodimer with MafK, it functions as a repressor of Maf recognition element (MARE) and transcription is repressed. Multiple alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, May 2009]","start":29194071,"end":29630751,"strand":1,"description":"BTB domain and CNC homolog 1 [Source:HGNC Symbol;Acc:HGNC:935]"}, {"versioned_ensembl_gene_id":"ENSG00000171970.12","gene_symbol":"ZNF57","gene_name":"zinc finger protein 57 [Source:HGNC Symbol;Acc:HGNC:13125]","synonyms":"ZNF424","biotype":"protein_coding","ncbi_id":"126295","summary":null,"start":2900898,"end":2918476,"strand":1,"description":"zinc finger protein 57 [Source:HGNC Symbol;Acc:HGNC:13125]"}, {"versioned_ensembl_gene_id":"ENSG00000267855.5","gene_symbol":"NDUFA7","gene_name":"NADH:ubiquinone oxidoreductase subunit A7 [Source:HGNC Symbol;Acc:HGNC:7691]","synonyms":"B14.5a","biotype":"protein_coding","ncbi_id":"4701","summary":"This gene encodes a subunit of NADH:ubiquinone oxidoreductase (complex I), which is a multiprotein complex located in the inner mitochondrial membrane. Complex I functions in the transfer of electrons from NADH to the respiratory chain. [provided by RefSeq, Mar 2011]","start":8308768,"end":8321396,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A7 [Source:HGNC Symbol;Acc:HGNC:7691]"}, {"versioned_ensembl_gene_id":"ENSG00000106346.11","gene_symbol":"USP42","gene_name":"ubiquitin specific peptidase 42 [Source:HGNC Symbol;Acc:HGNC:20068]","synonyms":"FLJ12697","biotype":"protein_coding","ncbi_id":"84132","summary":null,"start":6104884,"end":6161564,"strand":1,"description":"ubiquitin specific peptidase 42 [Source:HGNC Symbol;Acc:HGNC:20068]"}, {"versioned_ensembl_gene_id":"ENSG00000284479.1","gene_symbol":"AC009477.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":131035092,"end":131035262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255054.3","gene_symbol":"AL020996.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":25811470,"end":25823744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261986.1","gene_symbol":"KRT33A","gene_name":"keratin 33A [Source:HGNC Symbol;Acc:HGNC:6450]","synonyms":"KRTHA3A,Krt1-3,Ha-3I","biotype":"protein_coding","ncbi_id":"3883","summary":"This gene encodes a member of the keratin gene family. This gene is one of multiple type I hair keratin genes that are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. As a type I hair keratin, the encoded protein is an acidic protein which heterodimerizes with type II keratins to form hair and nails. There are two isoforms of this protein, encoded by two separate genes, keratin 33A and keratin 33B. [provided by RefSeq, May 2012]","start":41346092,"end":41350812,"strand":-1,"description":"keratin 33A [Source:HGNC Symbol;Acc:HGNC:6450]"}, {"versioned_ensembl_gene_id":"ENSG00000092200.12","gene_symbol":"RPGRIP1","gene_name":"retinitis pigmentosa GTPase regulator interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13436]","synonyms":"RPGRIP,RGI1,LCA6,CORD13","biotype":"protein_coding","ncbi_id":"57096","summary":"This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008]","start":21287939,"end":21351301,"strand":1,"description":"retinitis pigmentosa GTPase regulator interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13436]"}, {"versioned_ensembl_gene_id":"ENSG00000138100.13","gene_symbol":"TRIM54","gene_name":"tripartite motif containing 54 [Source:HGNC Symbol;Acc:HGNC:16008]","synonyms":"RNF30,MURF-3,MURF","biotype":"protein_coding","ncbi_id":"57159","summary":"The protein encoded by this gene contains a RING finger motif and is highly similar to the ring finger proteins RNF28/MURF1 and RNF29/MURF2. In vitro studies demonstrated that this protein, RNF28, and RNF29 form heterodimers, which may be important for the regulation of titin kinase and microtubule-dependent signal pathways in striated muscles. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":27282392,"end":27307439,"strand":1,"description":"tripartite motif containing 54 [Source:HGNC Symbol;Acc:HGNC:16008]"}, {"versioned_ensembl_gene_id":"ENSG00000198358.4","gene_symbol":"AL354714.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160932465,"end":160949922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235097.1","gene_symbol":"LINC00330","gene_name":"long intergenic non-protein coding RNA 330 [Source:HGNC Symbol;Acc:HGNC:42047]","synonyms":"NCRNA00330","biotype":"lincRNA","ncbi_id":"144817","summary":null,"start":44799503,"end":44809630,"strand":-1,"description":"long intergenic non-protein coding RNA 330 [Source:HGNC Symbol;Acc:HGNC:42047]"}, {"versioned_ensembl_gene_id":"ENSG00000220725.1","gene_symbol":"AL590290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55680642,"end":55681021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124370.10","gene_symbol":"MCEE","gene_name":"methylmalonyl-CoA epimerase [Source:HGNC Symbol;Acc:HGNC:16732]","synonyms":"GLOD2","biotype":"protein_coding","ncbi_id":"84693","summary":"The product of this gene catalyzes the interconversion of D- and L-methylmalonyl-CoA during the degradation of branched chain amino acids. odd chain-length fatty acids, and other metabolites. Mutations in this gene result in methylmalonyl-CoA epimerase deficiency, which is presented as mild to moderate methylmalonic aciduria. [provided by RefSeq, Jul 2008]","start":71109684,"end":71130239,"strand":-1,"description":"methylmalonyl-CoA epimerase [Source:HGNC Symbol;Acc:HGNC:16732]"}, {"versioned_ensembl_gene_id":"ENSG00000283683.1","gene_symbol":"MYOCOS","gene_name":"myocilin opposite strand [Source:HGNC Symbol;Acc:HGNC:53429]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":171600621,"end":171638799,"strand":1,"description":"myocilin opposite strand [Source:HGNC Symbol;Acc:HGNC:53429]"}, {"versioned_ensembl_gene_id":"ENSG00000262315.4","gene_symbol":"OR8U8","gene_name":"olfactory receptor family 8 subfamily U member 8 [Source:HGNC Symbol;Acc:HGNC:27538]","synonyms":null,"biotype":"protein_coding","ncbi_id":"504189","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56375625,"end":56376584,"strand":1,"description":"olfactory receptor family 8 subfamily U member 8 [Source:HGNC Symbol;Acc:HGNC:27538]"}, {"versioned_ensembl_gene_id":"ENSG00000247130.2","gene_symbol":"AC138781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":188140822,"end":188143379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274283.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54815911,"end":54830525,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000275247.1","gene_symbol":"GU182352.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54754487,"end":54766832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233720.1","gene_symbol":"AC245517.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22157382,"end":22157631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117640.17","gene_symbol":"MTFR1L","gene_name":"mitochondrial fission regulator 1 like [Source:HGNC Symbol;Acc:HGNC:28836]","synonyms":"FAM54B","biotype":"protein_coding","ncbi_id":"56181","summary":null,"start":25818640,"end":25832942,"strand":1,"description":"mitochondrial fission regulator 1 like [Source:HGNC Symbol;Acc:HGNC:28836]"}, {"versioned_ensembl_gene_id":"ENSG00000241553.12","gene_symbol":"ARPC4","gene_name":"actin related protein 2/3 complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:707]","synonyms":"p20-Arc,ARC20","biotype":"protein_coding","ncbi_id":"10093","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. This complex controls actin polymerization in cells and has been conserved throughout eukaryotic evolution. This gene encodes the p20 subunit, which is necessary for actin nucleation and high-affinity binding to F-actin. Alternative splicing results in multiple transcript variants. Naturally occurring read-through transcription exists between this gene and the downstream tubulin tyrosine ligase-like family, member 3 (TTLL3), which results in the production of a fusion protein. [provided by RefSeq, Nov 2010]","start":9792495,"end":9807726,"strand":1,"description":"actin related protein 2/3 complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:707]"}, {"versioned_ensembl_gene_id":"ENSG00000235424.1","gene_symbol":"SUMO2P10","gene_name":"SUMO2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49348]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481678","summary":null,"start":33077204,"end":33077491,"strand":1,"description":"SUMO2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49348]"}, {"versioned_ensembl_gene_id":"ENSG00000239857.6","gene_symbol":"GET4","gene_name":"golgi to ER traffic protein 4 [Source:HGNC Symbol;Acc:HGNC:21690]","synonyms":"H_NH1244M04.5,CGI-20,CEE,C7orf20,TRC35","biotype":"protein_coding","ncbi_id":"51608","summary":null,"start":876552,"end":896436,"strand":1,"description":"golgi to ER traffic protein 4 [Source:HGNC Symbol;Acc:HGNC:21690]"}, {"versioned_ensembl_gene_id":"ENSG00000273151.1","gene_symbol":"AC073957.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":879790,"end":886547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185532.15","gene_symbol":"PRKG1","gene_name":"protein kinase, cGMP-dependent, type I [Source:HGNC Symbol;Acc:HGNC:9414]","synonyms":"PRKGR1B,PRKG1B,PKG,PGK","biotype":"protein_coding","ncbi_id":"5592","summary":"Mammals have three different isoforms of cyclic GMP-dependent protein kinase (Ialpha, Ibeta, and II). These PRKG isoforms act as key mediators of the nitric oxide/cGMP signaling pathway and are important components of many signal transduction processes in diverse cell types. This PRKG1 gene on human chromosome 10 encodes the soluble Ialpha and Ibeta isoforms of PRKG by alternative transcript splicing. A separate gene on human chromosome 4, PRKG2, encodes the membrane-bound PRKG isoform II. The PRKG1 proteins play a central role in regulating cardiovascular and neuronal functions in addition to relaxing smooth muscle tone, preventing platelet aggregation, and modulating cell growth. This gene is most strongly expressed in all types of smooth muscle, platelets, cerebellar Purkinje cells, hippocampal neurons, and the lateral amygdala. Isoforms Ialpha and Ibeta have identical cGMP-binding and catalytic domains but differ in their leucine/isoleucine zipper and autoinhibitory sequences and therefore differ in their dimerization substrates and kinase enzyme activity. [provided by RefSeq, Sep 2011]","start":50991358,"end":52298350,"strand":1,"description":"protein kinase, cGMP-dependent, type I [Source:HGNC Symbol;Acc:HGNC:9414]"}, {"versioned_ensembl_gene_id":"ENSG00000215174.2","gene_symbol":"NLRP2B","gene_name":"NLR family pyrin domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29887]","synonyms":"NLRP2P,NALP2P,CLRX.1,POP4,NOD24","biotype":"protein_coding","ncbi_id":"286430","summary":null,"start":57677067,"end":57680260,"strand":-1,"description":"NLR family pyrin domain containing 2B [Source:HGNC Symbol;Acc:HGNC:29887]"}, {"versioned_ensembl_gene_id":"ENSG00000231132.1","gene_symbol":"AC022537.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51244894,"end":51245806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275056.1","gene_symbol":"AC020663.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4839244,"end":4840334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111261.13","gene_symbol":"MANSC1","gene_name":"MANSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25505]","synonyms":"LOH12CR3,FLJ10298","biotype":"protein_coding","ncbi_id":"54682","summary":null,"start":12326056,"end":12350541,"strand":-1,"description":"MANSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25505]"}, {"versioned_ensembl_gene_id":"ENSG00000260223.1","gene_symbol":"AC099511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76107283,"end":76147806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272741.1","gene_symbol":"AC069257.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":196248230,"end":196318222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261313.1","gene_symbol":"AC105430.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75838630,"end":75860867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213139.7","gene_symbol":"CRYGS","gene_name":"crystallin gamma S [Source:HGNC Symbol;Acc:HGNC:2417]","synonyms":"CRYG8","biotype":"protein_coding","ncbi_id":"1427","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. This gene encodes a protein initially considered to be a beta-crystallin but the encoded protein is monomeric and has greater sequence similarity to other gamma-crystallins. This gene encodes the most significant gamma-crystallin in adult eye lens tissue. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation. [provided by RefSeq, Jul 2008]","start":186538441,"end":186546702,"strand":-1,"description":"crystallin gamma S [Source:HGNC Symbol;Acc:HGNC:2417]"}, {"versioned_ensembl_gene_id":"ENSG00000259713.1","gene_symbol":"AC013391.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":89518523,"end":89591956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269504.1","gene_symbol":"AC003973.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22017959,"end":22036315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259615.1","gene_symbol":"AC013391.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89579765,"end":89582297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249279.5","gene_symbol":"LINC02057","gene_name":"long intergenic non-protein coding RNA 2057 [Source:HGNC Symbol;Acc:HGNC:52900]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378992","summary":null,"start":61201309,"end":61264929,"strand":-1,"description":"long intergenic non-protein coding RNA 2057 [Source:HGNC Symbol;Acc:HGNC:52900]"}, {"versioned_ensembl_gene_id":"ENSG00000259182.5","gene_symbol":"AC019254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101168530,"end":101170821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103494.12","gene_symbol":"RPGRIP1L","gene_name":"RPGRIP1 like [Source:HGNC Symbol;Acc:HGNC:29168]","synonyms":"FTM,CORS3,PPP1R134,NPHP8,MKS5,KIAA1005,JBTS7","biotype":"protein_coding","ncbi_id":"23322","summary":"The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]","start":53597683,"end":53703938,"strand":-1,"description":"RPGRIP1 like [Source:HGNC Symbol;Acc:HGNC:29168]"}, {"versioned_ensembl_gene_id":"ENSG00000090520.11","gene_symbol":"DNAJB11","gene_name":"DnaJ heat shock protein family (Hsp40) member B11 [Source:HGNC Symbol;Acc:HGNC:14889]","synonyms":"HEDJ,ERdj3,EDJ","biotype":"protein_coding","ncbi_id":"51726","summary":"This gene encodes a soluble glycoprotein of the endoplasmic reticulum (ER) lumen that functions as a co-chaperone of binding immunoglobulin protein, a 70 kilodalton heat shock protein chaperone required for the proper folding and assembly of proteins in the ER. The encoded protein contains a highly conserved J domain of about 70 amino acids with a characteristic His-Pro-Asp (HPD) motif and may regulate the activity of binding immunoglobulin protein by stimulating ATPase activity. [provided by RefSeq, Mar 2014]","start":186567403,"end":186585800,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B11 [Source:HGNC Symbol;Acc:HGNC:14889]"}, {"versioned_ensembl_gene_id":"ENSG00000073111.13","gene_symbol":"MCM2","gene_name":"minichromosome maintenance complex component 2 [Source:HGNC Symbol;Acc:HGNC:6944]","synonyms":"KIAA0030,D3S3194,CDCL1,cdc19,CCNL1,BM28","biotype":"protein_coding","ncbi_id":"4171","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein forms a complex with MCM4, 6, and 7, and has been shown to regulate the helicase activity of the complex. This protein is phosphorylated, and thus regulated by, protein kinases CDC2 and CDC7. Multiple alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been defined. [provided by RefSeq, Oct 2012]","start":127598223,"end":127622436,"strand":1,"description":"minichromosome maintenance complex component 2 [Source:HGNC Symbol;Acc:HGNC:6944]"}, {"versioned_ensembl_gene_id":"ENSG00000188725.7","gene_symbol":"SMIM15","gene_name":"small integral membrane protein 15 [Source:HGNC Symbol;Acc:HGNC:33861]","synonyms":"DKFZP686E2158,C5orf43","biotype":"protein_coding","ncbi_id":"643155","summary":null,"start":61157709,"end":61162474,"strand":-1,"description":"small integral membrane protein 15 [Source:HGNC Symbol;Acc:HGNC:33861]"}, {"versioned_ensembl_gene_id":"ENSG00000261630.1","gene_symbol":"AC007496.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53981229,"end":53981912,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225044.1","gene_symbol":"AC018814.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1962381,"end":1987470,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214073.2","gene_symbol":"RPL21P17","gene_name":"ribosomal protein L21 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:19416]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727810","summary":null,"start":1905651,"end":1906125,"strand":1,"description":"ribosomal protein L21 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:19416]"}, {"versioned_ensembl_gene_id":"ENSG00000186231.16","gene_symbol":"KLHL32","gene_name":"kelch like family member 32 [Source:HGNC Symbol;Acc:HGNC:21221]","synonyms":"KIAA1900,BKLHD5","biotype":"protein_coding","ncbi_id":"114792","summary":null,"start":96924620,"end":97140754,"strand":1,"description":"kelch like family member 32 [Source:HGNC Symbol;Acc:HGNC:21221]"}, {"versioned_ensembl_gene_id":"ENSG00000281425.1","gene_symbol":"AC243922.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70518623,"end":70529103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280518.1","gene_symbol":"AC244260.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70425738,"end":70449761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156265.15","gene_symbol":"MAP3K7CL","gene_name":"MAP3K7 C-terminal like [Source:HGNC Symbol;Acc:HGNC:16457]","synonyms":"TAKL-4,TAKL-2,TAKL-1,TAKL,TAK1L,C21orf7","biotype":"protein_coding","ncbi_id":"56911","summary":null,"start":29077471,"end":29175889,"strand":1,"description":"MAP3K7 C-terminal like [Source:HGNC Symbol;Acc:HGNC:16457]"}, {"versioned_ensembl_gene_id":"ENSG00000134072.10","gene_symbol":"CAMK1","gene_name":"calcium/calmodulin dependent protein kinase I [Source:HGNC Symbol;Acc:HGNC:1459]","synonyms":"CaMKI","biotype":"protein_coding","ncbi_id":"8536","summary":"Calcium/calmodulin-dependent protein kinase I is expressed in many tissues and is a component of a calmodulin-dependent protein kinase cascade. Calcium/calmodulin directly activates calcium/calmodulin-dependent protein kinase I by binding to the enzyme and indirectly promotes the phosphorylation and synergistic activation of the enzyme by calcium/calmodulin-dependent protein kinase I kinase. [provided by RefSeq, Jul 2008]","start":9757342,"end":9769992,"strand":-1,"description":"calcium/calmodulin dependent protein kinase I [Source:HGNC Symbol;Acc:HGNC:1459]"}, {"versioned_ensembl_gene_id":"ENSG00000149657.19","gene_symbol":"LSM14B","gene_name":"LSM family member 14B [Source:HGNC Symbol;Acc:HGNC:15887]","synonyms":"RAP55B,LSM13,FT005,FLJ25473,FAM61B,C20orf40,bA11M20.3","biotype":"protein_coding","ncbi_id":"149986","summary":null,"start":62122461,"end":62135378,"strand":1,"description":"LSM family member 14B [Source:HGNC Symbol;Acc:HGNC:15887]"}, {"versioned_ensembl_gene_id":"ENSG00000166813.14","gene_symbol":"KIF7","gene_name":"kinesin family member 7 [Source:HGNC Symbol;Acc:HGNC:30497]","synonyms":"JBTS12","biotype":"protein_coding","ncbi_id":"374654","summary":"This gene encodes a cilia-associated protein belonging to the kinesin family. This protein plays a role in the sonic hedgehog (SHH) signaling pathway through the regulation of GLI transcription factors. It functions as a negative regulator of the SHH pathway by preventing inappropriate activation of GLI2 in the absence of ligand, and as a positive regulator by preventing the processing of GLI3 into its repressor form. Mutations in this gene have been associated with various ciliopathies. [provided by RefSeq, Oct 2011]","start":89608789,"end":89655451,"strand":-1,"description":"kinesin family member 7 [Source:HGNC Symbol;Acc:HGNC:30497]"}, {"versioned_ensembl_gene_id":"ENSG00000165887.11","gene_symbol":"ANKRD2","gene_name":"ankyrin repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:495]","synonyms":"ARPP","biotype":"protein_coding","ncbi_id":"26287","summary":"This gene encodes a protein that belongs to the muscle ankyrin repeat protein (MARP) family. A similar gene in rodents is a component of a muscle stress response pathway and plays a role in the stretch-response associated with slow muscle function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":97572499,"end":97583884,"strand":1,"description":"ankyrin repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:495]"}, {"versioned_ensembl_gene_id":"ENSG00000283390.1","gene_symbol":"AC068631.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":186596976,"end":186597200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237491.8","gene_symbol":"AL669831.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":778770,"end":810060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198744.5","gene_symbol":"MTCO3P12","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52042]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075270","summary":null,"start":634376,"end":634922,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52042]"}, {"versioned_ensembl_gene_id":"ENSG00000250771.2","gene_symbol":"AC106865.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153640168,"end":153681180,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284662.1","gene_symbol":"OR4F16","gene_name":"olfactory receptor family 4 subfamily F member 16 [Source:HGNC Symbol;Acc:HGNC:15079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81399","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":685679,"end":686673,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 16 [Source:HGNC Symbol;Acc:HGNC:15079]"}, {"versioned_ensembl_gene_id":"ENSG00000248208.1","gene_symbol":"WDR45P1","gene_name":"WD repeat domain 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"594841","summary":null,"start":153658572,"end":153659653,"strand":1,"description":"WD repeat domain 45 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52406]"}, {"versioned_ensembl_gene_id":"ENSG00000268403.2","gene_symbol":"AC132192.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9459556,"end":9460702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165309.13","gene_symbol":"ARMC3","gene_name":"armadillo repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:30964]","synonyms":"FLJ32827,CT81","biotype":"protein_coding","ncbi_id":"219681","summary":"Armadillo/beta-catenin (CTNNB1; MIM 116806)-like (ARM) domains are imperfect 45-amino acid repeats involved in protein-protein interactions. ARM domain-containing proteins, such as ARMC3, function in signal transduction, development, cell adhesion and mobility, and tumor initiation and metastasis (Li et al., 2006 [PubMed 16915934]).[supplied by OMIM, Mar 2008]","start":22928024,"end":23038523,"strand":1,"description":"armadillo repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:30964]"}, {"versioned_ensembl_gene_id":"ENSG00000206444.9","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29788252,"end":29794972,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000237905.1","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29789145,"end":29790119,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000281915.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195738903,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000177757.2","gene_symbol":"FAM87B","gene_name":"family with sequence similarity 87 member B [Source:HGNC Symbol;Acc:HGNC:32236]","synonyms":"FLJ40008","biotype":"lincRNA","ncbi_id":"400728","summary":null,"start":817371,"end":819837,"strand":1,"description":"family with sequence similarity 87 member B [Source:HGNC Symbol;Acc:HGNC:32236]"}, {"versioned_ensembl_gene_id":"ENSG00000213090.2","gene_symbol":"AC007256.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":201410544,"end":201413308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230092.7","gene_symbol":"AL669831.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":800879,"end":817712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229376.3","gene_symbol":"CICP3","gene_name":"capicua transcriptional repressor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132630","summary":null,"start":722092,"end":724903,"strand":1,"description":"capicua transcriptional repressor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37742]"}, {"versioned_ensembl_gene_id":"ENSG00000104679.10","gene_symbol":"R3HCC1","gene_name":"R3H domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:27329]","synonyms":"DKFZp564N123","biotype":"protein_coding","ncbi_id":"203069","summary":null,"start":23270120,"end":23296279,"strand":1,"description":"R3H domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:HGNC:27329]"}, {"versioned_ensembl_gene_id":"ENSG00000225880.5","gene_symbol":"LINC00115","gene_name":"long intergenic non-protein coding RNA 115 [Source:HGNC Symbol;Acc:HGNC:26211]","synonyms":"NCRNA00115,FLJ22639","biotype":"lincRNA","ncbi_id":"79854","summary":null,"start":826206,"end":827522,"strand":-1,"description":"long intergenic non-protein coding RNA 115 [Source:HGNC Symbol;Acc:HGNC:26211]"}, {"versioned_ensembl_gene_id":"ENSG00000259408.2","gene_symbol":"AC010809.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33851785,"end":33856809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110446.10","gene_symbol":"SLC15A3","gene_name":"solute carrier family 15 member 3 [Source:HGNC Symbol;Acc:HGNC:18068]","synonyms":"PHT2,hPTR3","biotype":"protein_coding","ncbi_id":"51296","summary":null,"start":60937084,"end":60952530,"strand":-1,"description":"solute carrier family 15 member 3 [Source:HGNC Symbol;Acc:HGNC:18068]"}, {"versioned_ensembl_gene_id":"ENSG00000226859.1","gene_symbol":"LINC02051","gene_name":"long intergenic non-protein coding RNA 2051 [Source:HGNC Symbol;Acc:HGNC:52891]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986165","summary":null,"start":186476727,"end":186478370,"strand":1,"description":"long intergenic non-protein coding RNA 2051 [Source:HGNC Symbol;Acc:HGNC:52891]"}, {"versioned_ensembl_gene_id":"ENSG00000263160.6","gene_symbol":"TMEM50B","gene_name":"transmembrane protein 50B [Source:HGNC Symbol;Acc:HGNC:1280]","synonyms":"C21orf4","biotype":"protein_coding","ncbi_id":"757","summary":null,"start":33432485,"end":33489568,"strand":-1,"description":"transmembrane protein 50B [Source:HGNC Symbol;Acc:HGNC:1280]"}, {"versioned_ensembl_gene_id":"ENSG00000129152.3","gene_symbol":"MYOD1","gene_name":"myogenic differentiation 1 [Source:HGNC Symbol;Acc:HGNC:7611]","synonyms":"PUM,MYOD,MYF3,bHLHc1","biotype":"protein_coding","ncbi_id":"4654","summary":"This gene encodes a nuclear protein that belongs to the basic helix-loop-helix family of transcription factors and the myogenic factors subfamily. It regulates muscle cell differentiation by inducing cell cycle arrest, a prerequisite for myogenic initiation. The protein is also involved in muscle regeneration. It activates its own transcription which may stabilize commitment to myogenesis. [provided by RefSeq, Jul 2008]","start":17719568,"end":17722131,"strand":1,"description":"myogenic differentiation 1 [Source:HGNC Symbol;Acc:HGNC:7611]"}, {"versioned_ensembl_gene_id":"ENSG00000241119.1","gene_symbol":"UGT1A9","gene_name":"UDP glucuronosyltransferase family 1 member A9 [Source:HGNC Symbol;Acc:HGNC:12541]","synonyms":"UGT1AI,LUGP4,HLUGP4","biotype":"protein_coding","ncbi_id":"54600","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene is active on phenols. [provided by RefSeq, Jul 2008]","start":233671853,"end":233773300,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A9 [Source:HGNC Symbol;Acc:HGNC:12541]"}, {"versioned_ensembl_gene_id":"ENSG00000233832.1","gene_symbol":"AL590623.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38783004,"end":38783108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180116.15","gene_symbol":"C12orf40","gene_name":"chromosome 12 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:26846]","synonyms":"FLJ40126","biotype":"protein_coding","ncbi_id":"283461","summary":null,"start":39626167,"end":39908300,"strand":1,"description":"chromosome 12 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:26846]"}, {"versioned_ensembl_gene_id":"ENSG00000248747.1","gene_symbol":"AC107220.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141240739,"end":141278789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258035.1","gene_symbol":"AC123567.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94168006,"end":94186044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197183.14","gene_symbol":"NOL4L","gene_name":"nucleolar protein 4 like [Source:HGNC Symbol;Acc:HGNC:16106]","synonyms":"DKFZP566G1424,dJ1184F4.4,dJ1184F4.2,C20orf113,C20orf112","biotype":"protein_coding","ncbi_id":"140688","summary":null,"start":32443059,"end":32585074,"strand":-1,"description":"nucleolar protein 4 like [Source:HGNC Symbol;Acc:HGNC:16106]"}, {"versioned_ensembl_gene_id":"ENSG00000228156.1","gene_symbol":"AL133343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32581963,"end":32593900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237634.1","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"C6orf100,dJ25J6.5","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28940401,"end":28941061,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000273918.1","gene_symbol":"AC245128.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151229.12","gene_symbol":"SLC2A13","gene_name":"solute carrier family 2 member 13 [Source:HGNC Symbol;Acc:HGNC:15956]","synonyms":"HMIT","biotype":"protein_coding","ncbi_id":"114134","summary":null,"start":39755021,"end":40106089,"strand":-1,"description":"solute carrier family 2 member 13 [Source:HGNC Symbol;Acc:HGNC:15956]"}, {"versioned_ensembl_gene_id":"ENSG00000259402.1","gene_symbol":"AC090515.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58815272,"end":58817728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224470.7","gene_symbol":"ATXN1L","gene_name":"ataxin 1 like [Source:HGNC Symbol;Acc:HGNC:33279]","synonyms":"BOAT1","biotype":"protein_coding","ncbi_id":"342371","summary":null,"start":71845991,"end":71885268,"strand":1,"description":"ataxin 1 like [Source:HGNC Symbol;Acc:HGNC:33279]"}, {"versioned_ensembl_gene_id":"ENSG00000261633.1","gene_symbol":"AC018552.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57622034,"end":57631647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267205.1","gene_symbol":"AC005954.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3753840,"end":3756517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011132.11","gene_symbol":"APBA3","gene_name":"amyloid beta precursor protein binding family A member 3 [Source:HGNC Symbol;Acc:HGNC:580]","synonyms":"X11L2,mint3","biotype":"protein_coding","ncbi_id":"9546","summary":"The protein encoded by this gene is a member of the X11 protein family. It is an adapter protein that interacts with the Alzheimer's disease amyloid precursor protein. This gene product is believed to be involved in signal transduction processes. This gene is a candidate gene for Alzheimer's disease. [provided by RefSeq, Jul 2008]","start":3750819,"end":3761699,"strand":-1,"description":"amyloid beta precursor protein binding family A member 3 [Source:HGNC Symbol;Acc:HGNC:580]"}, {"versioned_ensembl_gene_id":"ENSG00000280075.1","gene_symbol":"AC018692.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9810381,"end":9810503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000001167.14","gene_symbol":"NFYA","gene_name":"nuclear transcription factor Y subunit alpha [Source:HGNC Symbol;Acc:HGNC:7804]","synonyms":"HAP2,NF-YA,CBF-B","biotype":"protein_coding","ncbi_id":"4800","summary":"The protein encoded by this gene is one subunit of a trimeric complex, forming a highly conserved transcription factor that binds to CCAAT motifs in the promoter regions in a variety of genes. Subunit A associates with a tight dimer composed of the B and C subunits, resulting in a trimer that binds to DNA with high specificity and affinity. The sequence specific interactions of the complex are made by the A subunit, suggesting a role as the regulatory subunit. In addition, there is evidence of post-transcriptional regulation in this gene product, either by protein degradation or control of translation. Further regulation is represented by alternative splicing in the glutamine-rich activation domain, with clear tissue-specific preferences for the two isoforms. [provided by RefSeq, Jul 2008]","start":41072945,"end":41099976,"strand":1,"description":"nuclear transcription factor Y subunit alpha [Source:HGNC Symbol;Acc:HGNC:7804]"}, {"versioned_ensembl_gene_id":"ENSG00000214940.8","gene_symbol":"NPIPA8","gene_name":"nuclear pore complex interacting protein family member A8 [Source:HGNC Symbol;Acc:HGNC:41983]","synonyms":"LCR16a9","biotype":"protein_coding","ncbi_id":"101059953","summary":null,"start":18317942,"end":18336736,"strand":-1,"description":"nuclear pore complex interacting protein family member A8 [Source:HGNC Symbol;Acc:HGNC:41983]"}, {"versioned_ensembl_gene_id":"ENSG00000217331.1","gene_symbol":"AL355143.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96672129,"end":96672969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272851.1","gene_symbol":"AC096772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":207753872,"end":207754435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276484.1","gene_symbol":"AC126755.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18313294,"end":18316984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250372.1","gene_symbol":"MARK2P4","gene_name":"microtubule affinity regulating kinase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39795]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421496","summary":null,"start":176012038,"end":176014417,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39795]"}, {"versioned_ensembl_gene_id":"ENSG00000216518.1","gene_symbol":"EEF1GP6","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421733","summary":null,"start":96750824,"end":96751728,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44561]"}, {"versioned_ensembl_gene_id":"ENSG00000205746.9","gene_symbol":"AC126755.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18334400,"end":18352476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227860.1","gene_symbol":"MTND5P18","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42302]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873271","summary":null,"start":237949736,"end":237951536,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:42302]"}, {"versioned_ensembl_gene_id":"ENSG00000103056.11","gene_symbol":"SMPD3","gene_name":"sphingomyelin phosphodiesterase 3 [Source:HGNC Symbol;Acc:HGNC:14240]","synonyms":"NSMASE2","biotype":"protein_coding","ncbi_id":"55512","summary":null,"start":68358325,"end":68448688,"strand":-1,"description":"sphingomyelin phosphodiesterase 3 [Source:HGNC Symbol;Acc:HGNC:14240]"}, {"versioned_ensembl_gene_id":"ENSG00000227762.4","gene_symbol":"GUSBP8","gene_name":"glucuronidase, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42322]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441066","summary":null,"start":99532628,"end":99534611,"strand":1,"description":"glucuronidase, beta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42322]"}, {"versioned_ensembl_gene_id":"ENSG00000229120.2","gene_symbol":"CYCSP4","gene_name":"cytochrome c, somatic pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:24413]","synonyms":"HCP4","biotype":"processed_pseudogene","ncbi_id":"360157","summary":null,"start":202369526,"end":202370145,"strand":-1,"description":"cytochrome c, somatic pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:24413]"}, {"versioned_ensembl_gene_id":"ENSG00000167799.9","gene_symbol":"NUDT8","gene_name":"nudix hydrolase 8 [Source:HGNC Symbol;Acc:HGNC:8055]","synonyms":"FLJ41567","biotype":"protein_coding","ncbi_id":"254552","summary":null,"start":67627938,"end":67629930,"strand":-1,"description":"nudix hydrolase 8 [Source:HGNC Symbol;Acc:HGNC:8055]"}, {"versioned_ensembl_gene_id":"ENSG00000271318.1","gene_symbol":"AP000654.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86821143,"end":86821728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115687.13","gene_symbol":"PASK","gene_name":"PAS domain containing serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:17270]","synonyms":"STK37,PASKIN,KIAA0135","biotype":"protein_coding","ncbi_id":"23178","summary":"This gene encodes a member of the serine/threonine kinase family that contains two PAS domains. Expression of this gene is regulated by glucose, and the encoded protein plays a role in the regulation of insulin gene expression. Downregulation of this gene may play a role in type 2 diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":241106099,"end":241150264,"strand":-1,"description":"PAS domain containing serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:17270]"}, {"versioned_ensembl_gene_id":"ENSG00000276406.1","gene_symbol":"AC015726.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19868568,"end":19868689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227386.1","gene_symbol":"AC091705.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25547762,"end":25551062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264193.1","gene_symbol":"AC027229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25953216,"end":25953468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278966.2","gene_symbol":"AL031602.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32973553,"end":32974463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258943.1","gene_symbol":"AL049871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63298126,"end":63299547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267581.1","gene_symbol":"AC011477.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19761038,"end":19821716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282925.1","gene_symbol":"AC010424.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127588746,"end":127590710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266904.5","gene_symbol":"LINC00663","gene_name":"long intergenic non-protein coding RNA 663 [Source:HGNC Symbol;Acc:HGNC:28609]","synonyms":"MGC39821","biotype":"lincRNA","ncbi_id":"284440","summary":null,"start":19757366,"end":19776423,"strand":-1,"description":"long intergenic non-protein coding RNA 663 [Source:HGNC Symbol;Acc:HGNC:28609]"}, {"versioned_ensembl_gene_id":"ENSG00000254731.1","gene_symbol":"AP003059.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86703099,"end":86714092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130725.7","gene_symbol":"UBE2M","gene_name":"ubiquitin conjugating enzyme E2 M [Source:HGNC Symbol;Acc:HGNC:12491]","synonyms":"UBC12,hUbc12","biotype":"protein_coding","ncbi_id":"9040","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein is linked with a ubiquitin-like protein, NEDD8, which can be conjugated to cellular proteins, such as Cdc53/culin. [provided by RefSeq, Jul 2008]","start":58555712,"end":58558960,"strand":-1,"description":"ubiquitin conjugating enzyme E2 M [Source:HGNC Symbol;Acc:HGNC:12491]"}, {"versioned_ensembl_gene_id":"ENSG00000131051.22","gene_symbol":"RBM39","gene_name":"RNA binding motif protein 39 [Source:HGNC Symbol;Acc:HGNC:15923]","synonyms":"RNPC2,HCC1,fSAP59,CC1.3,CAPERalpha,CAPER","biotype":"protein_coding","ncbi_id":"9584","summary":"This gene encodes a member of the U2AF65 family of proteins. The encoded protein is found in the nucleus, where it co-localizes with core spliceosomal proteins. It has been shown to play a role in both steroid hormone receptor-mediated transcription and alternative splicing, and it is also a transcriptional coregulator of the viral oncoprotein v-Rel. Multiple transcript variants have been observed for this gene. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Aug 2011]","start":35701347,"end":35742312,"strand":-1,"description":"RNA binding motif protein 39 [Source:HGNC Symbol;Acc:HGNC:15923]"}, {"versioned_ensembl_gene_id":"ENSG00000181481.13","gene_symbol":"RNF135","gene_name":"ring finger protein 135 [Source:HGNC Symbol;Acc:HGNC:21158]","synonyms":"MGC13061","biotype":"protein_coding","ncbi_id":"84282","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":30968785,"end":30999911,"strand":1,"description":"ring finger protein 135 [Source:HGNC Symbol;Acc:HGNC:21158]"}, {"versioned_ensembl_gene_id":"ENSG00000251311.1","gene_symbol":"LINC02214","gene_name":"long intergenic non-protein coding RNA 2214 [Source:HGNC Symbol;Acc:HGNC:53081]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467223","summary":null,"start":116742991,"end":116762209,"strand":-1,"description":"long intergenic non-protein coding RNA 2214 [Source:HGNC Symbol;Acc:HGNC:53081]"}, {"versioned_ensembl_gene_id":"ENSG00000229720.1","gene_symbol":"AL109924.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169034197,"end":169035642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253245.2","gene_symbol":"MTND1P36","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:42086]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506721","summary":null,"start":103407441,"end":103408376,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:42086]"}, {"versioned_ensembl_gene_id":"ENSG00000138675.16","gene_symbol":"FGF5","gene_name":"fibroblast growth factor 5 [Source:HGNC Symbol;Acc:HGNC:3683]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2250","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified as an oncogene, which confers transforming potential when transfected into mammalian cells. Targeted disruption of the homolog of this gene in mouse resulted in the phenotype of abnormally long hair, which suggested a function as an inhibitor of hair elongation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":80266599,"end":80336680,"strand":1,"description":"fibroblast growth factor 5 [Source:HGNC Symbol;Acc:HGNC:3683]"}, {"versioned_ensembl_gene_id":"ENSG00000187266.13","gene_symbol":"EPOR","gene_name":"erythropoietin receptor [Source:HGNC Symbol;Acc:HGNC:3416]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2057","summary":"This gene encodes the erythropoietin receptor which is a member of the cytokine receptor family. Upon erythropoietin binding, this receptor activates Jak2 tyrosine kinase which activates different intracellular pathways including: Ras/MAP kinase, phosphatidylinositol 3-kinase and STAT transcription factors. The stimulated erythropoietin receptor appears to have a role in erythroid cell survival. Defects in the erythropoietin receptor may produce erythroleukemia and familial erythrocytosis. Dysregulation of this gene may affect the growth of certain tumors. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":11377205,"end":11384342,"strand":-1,"description":"erythropoietin receptor [Source:HGNC Symbol;Acc:HGNC:3416]"}, {"versioned_ensembl_gene_id":"ENSG00000196177.12","gene_symbol":"ACADSB","gene_name":"acyl-CoA dehydrogenase, short/branched chain [Source:HGNC Symbol;Acc:HGNC:91]","synonyms":"ACAD7,SBCAD","biotype":"protein_coding","ncbi_id":"36","summary":"Short/branched chain acyl-CoA dehydrogenase(ACADSB) is a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. Substrate specificity is the primary characteristic used to define members of this gene family. The ACADSB gene product has the greatest activity towards the short branched chain acyl-CoA derivative, (S)-2-methylbutyryl-CoA, but also reacts significantly with other 2-methyl branched chain substrates and with short straight chain acyl-CoAs. The cDNA encodes for a mitochondrial precursor protein which is cleaved upon mitochondrial import and predicted to yield a mature peptide of approximately 43.7-KDa. [provided by RefSeq, Jul 2008]","start":123008979,"end":123058311,"strand":1,"description":"acyl-CoA dehydrogenase, short/branched chain [Source:HGNC Symbol;Acc:HGNC:91]"}, {"versioned_ensembl_gene_id":"ENSG00000258995.1","gene_symbol":"PARP1P2","gene_name":"poly(ADP-ribose) polymerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:276]","synonyms":"PPOLP2,ADPRTP2","biotype":"processed_pseudogene","ncbi_id":"145","summary":null,"start":63123007,"end":63123201,"strand":1,"description":"poly(ADP-ribose) polymerase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:276]"}, {"versioned_ensembl_gene_id":"ENSG00000131941.7","gene_symbol":"RHPN2","gene_name":"rhophilin Rho GTPase binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85415","summary":"This gene encodes a member of the rhophilin family of Ras-homologous (Rho)-GTPase binding proteins. The encoded protein binds both GTP- and GDP-bound RhoA and GTP-bound RhoB and may be involved in the organization of the actin cytoskeleton. [provided by RefSeq, Apr 2009]","start":32978593,"end":33064888,"strand":-1,"description":"rhophilin Rho GTPase binding protein 2 [Source:HGNC Symbol;Acc:HGNC:19974]"}, {"versioned_ensembl_gene_id":"ENSG00000236919.3","gene_symbol":"AC109635.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50246554,"end":50247761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258877.2","gene_symbol":"ATP5A1P4","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23563]","synonyms":"ATP5AP4","biotype":"processed_pseudogene","ncbi_id":"100129782","summary":null,"start":62604113,"end":62605717,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23563]"}, {"versioned_ensembl_gene_id":"ENSG00000255946.1","gene_symbol":"AC069234.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120740470,"end":120761592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166272.16","gene_symbol":"WBP1L","gene_name":"WW domain binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:23510]","synonyms":"OPAL1,FLJ20154,C10orf26","biotype":"protein_coding","ncbi_id":"54838","summary":null,"start":102743970,"end":102816267,"strand":1,"description":"WW domain binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:23510]"}, {"versioned_ensembl_gene_id":"ENSG00000275540.1","gene_symbol":"AC011477.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19740884,"end":19750127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270402.1","gene_symbol":"AC011458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19708965,"end":19710465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259135.1","gene_symbol":"AL445363.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34556774,"end":34561298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234642.8","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32918409,"end":32919085,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000258917.1","gene_symbol":"ZMYND19P1","gene_name":"zinc finger MYND-type containing 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421055","summary":null,"start":77696591,"end":77697377,"strand":1,"description":"zinc finger MYND-type containing 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44540]"}, {"versioned_ensembl_gene_id":"ENSG00000136122.15","gene_symbol":"BORA","gene_name":"bora, aurora kinase A activator [Source:HGNC Symbol;Acc:HGNC:24724]","synonyms":"FLJ22624,C13orf34","biotype":"protein_coding","ncbi_id":"79866","summary":"BORA is an activator of the protein kinase Aurora A (AURKA; MIM 603072), which is required for centrosome maturation, spindle assembly, and asymmetric protein localization during mitosis (Hutterer et al., 2006 [PubMed 16890155]).[supplied by OMIM, Mar 2008]","start":72727749,"end":72756198,"strand":1,"description":"bora, aurora kinase A activator [Source:HGNC Symbol;Acc:HGNC:24724]"}, {"versioned_ensembl_gene_id":"ENSG00000239272.1","gene_symbol":"RPL21P10","gene_name":"ribosomal protein L21 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:19795]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319143","summary":null,"start":77683202,"end":77683989,"strand":-1,"description":"ribosomal protein L21 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:19795]"}, {"versioned_ensembl_gene_id":"ENSG00000249413.2","gene_symbol":"AC116049.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65998846,"end":66150012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272304.1","gene_symbol":"AC096721.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66003281,"end":66016792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248238.1","gene_symbol":"LINC02438","gene_name":"long intergenic non-protein coding RNA 2438 [Source:HGNC Symbol;Acc:HGNC:53370]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986264","summary":null,"start":19172335,"end":19456994,"strand":-1,"description":"long intergenic non-protein coding RNA 2438 [Source:HGNC Symbol;Acc:HGNC:53370]"}, {"versioned_ensembl_gene_id":"ENSG00000100601.9","gene_symbol":"ALKBH1","gene_name":"alkB homolog 1, histone H2A dioxygenase [Source:HGNC Symbol;Acc:HGNC:17911]","synonyms":"hABH,ALKBH,alkB,ABH","biotype":"protein_coding","ncbi_id":"8846","summary":"This gene encodes a homolog to the E. coli alkB gene product. The E. coli alkB protein is part of the adaptive response mechanism of DNA alkylation damage repair. It is involved in damage reversal by oxidative demethylation of 1-methyladenine and 3-methylcytosine. [provided by RefSeq, Jul 2008]","start":77672404,"end":77708020,"strand":-1,"description":"alkB homolog 1, histone H2A dioxygenase [Source:HGNC Symbol;Acc:HGNC:17911]"}, {"versioned_ensembl_gene_id":"ENSG00000271930.1","gene_symbol":"AC016877.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98943595,"end":98944098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151687.14","gene_symbol":"ANKAR","gene_name":"ankyrin and armadillo repeat containing [Source:HGNC Symbol;Acc:HGNC:26350]","synonyms":"FLJ25415","biotype":"protein_coding","ncbi_id":"150709","summary":null,"start":189674290,"end":189761193,"strand":1,"description":"ankyrin and armadillo repeat containing [Source:HGNC Symbol;Acc:HGNC:26350]"}, {"versioned_ensembl_gene_id":"ENSG00000227927.2","gene_symbol":"MACROD2-IT1","gene_name":"MACROD2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:16201]","synonyms":"NCRNA00227,C20orf68,bA467D7.4","biotype":"sense_intronic","ncbi_id":"140848","summary":null,"start":14554384,"end":14636524,"strand":1,"description":"MACROD2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:16201]"}, {"versioned_ensembl_gene_id":"ENSG00000169045.17","gene_symbol":"HNRNPH1","gene_name":"heterogeneous nuclear ribonucleoprotein H1 [Source:HGNC Symbol;Acc:HGNC:5041]","synonyms":"hnRNPH,HNRPH1","biotype":"protein_coding","ncbi_id":"3187","summary":"This gene encodes a member of a subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA. These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some may shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNA and is very similar to the family member HNRPF. This gene may be associated with hereditary lymphedema type I. Alternatively spliced transcript variants have been described [provided by RefSeq, Mar 2012]","start":179614178,"end":179634784,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein H1 [Source:HGNC Symbol;Acc:HGNC:5041]"}, {"versioned_ensembl_gene_id":"ENSG00000129559.12","gene_symbol":"NEDD8","gene_name":"neural precursor cell expressed, developmentally down-regulated 8 [Source:HGNC Symbol;Acc:HGNC:7732]","synonyms":"Nedd-8","biotype":"protein_coding","ncbi_id":"4738","summary":null,"start":24216852,"end":24232454,"strand":-1,"description":"neural precursor cell expressed, developmentally down-regulated 8 [Source:HGNC Symbol;Acc:HGNC:7732]"}, {"versioned_ensembl_gene_id":"ENSG00000165630.13","gene_symbol":"PRPF18","gene_name":"pre-mRNA processing factor 18 [Source:HGNC Symbol;Acc:HGNC:17351]","synonyms":"hPrp18","biotype":"protein_coding","ncbi_id":"8559","summary":"Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is found to be essential for the catalytic step II in pre-mRNA splicing process. It is found in the spliceosome, and contains seven WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to the yeast splicing factor Prp18. [provided by RefSeq, Jul 2008]","start":13586927,"end":13630868,"strand":1,"description":"pre-mRNA processing factor 18 [Source:HGNC Symbol;Acc:HGNC:17351]"}, {"versioned_ensembl_gene_id":"ENSG00000152784.15","gene_symbol":"PRDM8","gene_name":"PR/SET domain 8 [Source:HGNC Symbol;Acc:HGNC:13993]","synonyms":"KMT8D","biotype":"protein_coding","ncbi_id":"56978","summary":"This gene encodes a protein that belongs to a conserved family of histone methyltransferases that predominantly act as negative regulators of transcription. The encoded protein contains an N-terminal Su(var)3-9, Enhancer-of-zeste, and Trithorax (SET) domain and a double zinc-finger domain. Knockout of this gene in mouse results in mistargeting by neurons of the dorsal telencephalon, abnormal itch-like behavior, and impaired differentiation of rod bipolar cells. In humans, the protein has been shown to interact with the phosphatase laforin and the ubiquitin ligase malin, which regulate glycogen construction in the cytoplasm. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":80183879,"end":80204329,"strand":1,"description":"PR/SET domain 8 [Source:HGNC Symbol;Acc:HGNC:13993]"}, {"versioned_ensembl_gene_id":"ENSG00000139144.9","gene_symbol":"PIK3C2G","gene_name":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma [Source:HGNC Symbol;Acc:HGNC:8973]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5288","summary":"The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. This gene may play a role in several diseases, including type II diabetes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":18247614,"end":18648416,"strand":1,"description":"phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma [Source:HGNC Symbol;Acc:HGNC:8973]"}, {"versioned_ensembl_gene_id":"ENSG00000235067.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30710458,"end":30715683,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000248719.1","gene_symbol":"AC021127.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80183280,"end":80190169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255111.1","gene_symbol":"AP006587.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49892262,"end":49893777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169583.12","gene_symbol":"CLIC3","gene_name":"chloride intracellular channel 3 [Source:HGNC Symbol;Acc:HGNC:2064]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9022","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 3 is a member of the p64 family and is predominantly localized in the nucleus and stimulates chloride ion channel activity. In addition, this protein may participate in cellular growth control, based on its association with ERK7, a member of the MAP kinase family. [provided by RefSeq, Jul 2008]","start":136994635,"end":136996803,"strand":-1,"description":"chloride intracellular channel 3 [Source:HGNC Symbol;Acc:HGNC:2064]"}, {"versioned_ensembl_gene_id":"ENSG00000243669.2","gene_symbol":"AP000926.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123035867,"end":123036224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213184.3","gene_symbol":"AP003040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123017638,"end":123018661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248215.5","gene_symbol":"LINC02505","gene_name":"long intergenic non-protein coding RNA 2505 [Source:HGNC Symbol;Acc:HGNC:53494]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374400","summary":null,"start":36496537,"end":36641900,"strand":-1,"description":"long intergenic non-protein coding RNA 2505 [Source:HGNC Symbol;Acc:HGNC:53494]"}, {"versioned_ensembl_gene_id":"ENSG00000124145.6","gene_symbol":"SDC4","gene_name":"syndecan 4 [Source:HGNC Symbol;Acc:HGNC:10661]","synonyms":"amphiglycan,SYND4,ryudocan","biotype":"protein_coding","ncbi_id":"6385","summary":"The protein encoded by this gene is a transmembrane (type I) heparan sulfate proteoglycan that functions as a receptor in intracellular signaling. The encoded protein is found as a homodimer and is a member of the syndecan proteoglycan family. This gene is found on chromosome 20, while a pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008]","start":45325288,"end":45348424,"strand":-1,"description":"syndecan 4 [Source:HGNC Symbol;Acc:HGNC:10661]"}, {"versioned_ensembl_gene_id":"ENSG00000234698.1","gene_symbol":"AL161937.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50166362,"end":50171742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237756.1","gene_symbol":"AL592435.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163259850,"end":163260659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111652.9","gene_symbol":"COPS7A","gene_name":"COP9 signalosome subunit 7A [Source:HGNC Symbol;Acc:HGNC:16758]","synonyms":"CSN7A","biotype":"protein_coding","ncbi_id":"50813","summary":"This gene encodes a component of the COP9 signalosome, an evolutionarily conserved multi-subunit protease that regulates the activity of the ubiquitin conjugation pathway. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Mar 2014]","start":6723741,"end":6731875,"strand":1,"description":"COP9 signalosome subunit 7A [Source:HGNC Symbol;Acc:HGNC:16758]"}, {"versioned_ensembl_gene_id":"ENSG00000131849.11","gene_symbol":"ZNF132","gene_name":"zinc finger protein 132 [Source:HGNC Symbol;Acc:HGNC:12916]","synonyms":"pHZ-12","biotype":"protein_coding","ncbi_id":"7691","summary":null,"start":58432814,"end":58440222,"strand":-1,"description":"zinc finger protein 132 [Source:HGNC Symbol;Acc:HGNC:12916]"}, {"versioned_ensembl_gene_id":"ENSG00000227694.1","gene_symbol":"RPL23AP74","gene_name":"ribosomal protein L23a pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:36148]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729617","summary":null,"start":61069871,"end":61070341,"strand":1,"description":"ribosomal protein L23a pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:36148]"}, {"versioned_ensembl_gene_id":"ENSG00000225457.1","gene_symbol":"AC073346.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":113100663,"end":113146330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269473.1","gene_symbol":"AC012313.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58440448,"end":58445849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170486.10","gene_symbol":"KRT72","gene_name":"keratin 72 [Source:HGNC Symbol;Acc:HGNC:28932]","synonyms":"KRT6IRS2,KRT6,K6IRS2,K6irs","biotype":"protein_coding","ncbi_id":"140807","summary":"Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells. The type II keratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This gene encodes a type II keratin that is specifically expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q12-q13. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2009]","start":52585589,"end":52601538,"strand":-1,"description":"keratin 72 [Source:HGNC Symbol;Acc:HGNC:28932]"}, {"versioned_ensembl_gene_id":"ENSG00000162621.6","gene_symbol":"LRRC53","gene_name":"leucine rich repeat containing 53 [Source:HGNC Symbol;Acc:HGNC:25255]","synonyms":null,"biotype":"protein_coding","ncbi_id":"105378803","summary":null,"start":74469878,"end":74512614,"strand":-1,"description":"leucine rich repeat containing 53 [Source:HGNC Symbol;Acc:HGNC:25255]"}, {"versioned_ensembl_gene_id":"ENSG00000237324.3","gene_symbol":"AC093158.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74341579,"end":74378802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173409.13","gene_symbol":"ARV1","gene_name":"ARV1 homolog, fatty acid homeostasis modulator [Source:HGNC Symbol;Acc:HGNC:29561]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64801","summary":"this gene encodes a transmembrane protein that contains a conserved zinc ribbon motif at the N- terminus. A similar protein in mouse is thought to function in fatty acid homeostasis. Mutations in this gene are associated with early infantile epileptic encephalopathy 38. [provided by RefSeq, Nov 2016]","start":230978981,"end":231000595,"strand":1,"description":"ARV1 homolog, fatty acid homeostasis modulator [Source:HGNC Symbol;Acc:HGNC:29561]"}, {"versioned_ensembl_gene_id":"ENSG00000164604.12","gene_symbol":"GPR85","gene_name":"G protein-coupled receptor 85 [Source:HGNC Symbol;Acc:HGNC:4536]","synonyms":"SREB2","biotype":"protein_coding","ncbi_id":"54329","summary":"Members of the G protein-coupled receptor (GPCR) family, such as GPR85, have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli, such as neurotransmitters, hormones, or light, induces an intracellular signaling cascade mediated by heterotrimeric GTP-binding proteins, or G proteins (Matsumoto et al., 2000 [PubMed 10833454]).[supplied by OMIM, Aug 2008]","start":113078331,"end":113087778,"strand":-1,"description":"G protein-coupled receptor 85 [Source:HGNC Symbol;Acc:HGNC:4536]"}, {"versioned_ensembl_gene_id":"ENSG00000279658.1","gene_symbol":"AC110491.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":97836986,"end":97874691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127666.9","gene_symbol":"TICAM1","gene_name":"toll like receptor adaptor molecule 1 [Source:HGNC Symbol;Acc:HGNC:18348]","synonyms":"MGC35334,TRIF,TICAM-1,PRVTIRB","biotype":"protein_coding","ncbi_id":"148022","summary":"This gene encodes an adaptor protein containing a Toll/interleukin-1 receptor (TIR) homology domain, which is an intracellular signaling domain that mediates protein-protein interactions between the Toll-like receptors (TLRs) and signal-transduction components. This protein is involved in native immunity against invading pathogens. It specifically interacts with toll-like receptor 3, but not with other TLRs, and this association mediates dsRNA induction of interferon-beta through activation of nuclear factor kappa-B, during an antiviral immune response. Mutations in this gene are associated with encephalopathy, acute, infection-induced. [provided by RefSeq, Jul 2020]","start":4815932,"end":4831704,"strand":-1,"description":"toll like receptor adaptor molecule 1 [Source:HGNC Symbol;Acc:HGNC:18348]"}, {"versioned_ensembl_gene_id":"ENSG00000254112.1","gene_symbol":"AP003467.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98633547,"end":98633865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148488.15","gene_symbol":"ST8SIA6","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:23317]","synonyms":"SIAT8F","biotype":"protein_coding","ncbi_id":"338596","summary":"This gene encodes a member of the glycosyltransferase 29 protein family. Members of this protein family synthesize sialylglycoconjugates. Sialylation may contribute to multidrug resistance in cancer cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":17318383,"end":17454330,"strand":-1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:23317]"}, {"versioned_ensembl_gene_id":"ENSG00000144596.12","gene_symbol":"GRIP2","gene_name":"glutamate receptor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23841]","synonyms":"KIAA1719","biotype":"protein_coding","ncbi_id":"80852","summary":null,"start":14489111,"end":14556075,"strand":-1,"description":"glutamate receptor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23841]"}, {"versioned_ensembl_gene_id":"ENSG00000204832.9","gene_symbol":"ST8SIA6-AS1","gene_name":"ST8SIA6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44880]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128098","summary":null,"start":17386936,"end":17413503,"strand":1,"description":"ST8SIA6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44880]"}, {"versioned_ensembl_gene_id":"ENSG00000157077.14","gene_symbol":"ZFYVE9","gene_name":"zinc finger FYVE-type containing 9 [Source:HGNC Symbol;Acc:HGNC:6775]","synonyms":"SMADIP,SARA,PPP1R173,MADHIP","biotype":"protein_coding","ncbi_id":"9372","summary":"This gene encodes a double zinc finger motif-containing protein that participates in the transforming growth factor-beta (TGFB) signalling pathway. The encoded protein interacts directly with SMAD2 and SMAD3, and recruits SMAD2 to the TGFB receptor. There are multiple pseudogenes for this gene on chromosomes 2, 15, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":52142094,"end":52346686,"strand":1,"description":"zinc finger FYVE-type containing 9 [Source:HGNC Symbol;Acc:HGNC:6775]"}, {"versioned_ensembl_gene_id":"ENSG00000277010.1","gene_symbol":"AC120498.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1223639,"end":1224143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250185.2","gene_symbol":"RCC2P8","gene_name":"regulator of chromosome condensation 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42384]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129714","summary":null,"start":108788745,"end":108789779,"strand":-1,"description":"regulator of chromosome condensation 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42384]"}, {"versioned_ensembl_gene_id":"ENSG00000234546.3","gene_symbol":"LINC01759","gene_name":"long intergenic non-protein coding RNA 1759 [Source:HGNC Symbol;Acc:HGNC:52548]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724571","summary":null,"start":9182004,"end":9196284,"strand":1,"description":"long intergenic non-protein coding RNA 1759 [Source:HGNC Symbol;Acc:HGNC:52548]"}, {"versioned_ensembl_gene_id":"ENSG00000163464.7","gene_symbol":"CXCR1","gene_name":"C-X-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:6026]","synonyms":"IL8RA,CMKAR1,CKR-1,CDw128a,CD181","biotype":"protein_coding","ncbi_id":"3577","summary":"The protein encoded by this gene is a member of the G-protein-coupled receptor family. This protein is a receptor for interleukin 8 (IL8). It binds to IL8 with high affinity, and transduces the signal through a G-protein activated second messenger system. Knockout studies in mice suggested that this protein inhibits embryonic oligodendrocyte precursor migration in developing spinal cord. This gene, IL8RB, a gene encoding another high affinity IL8 receptor, as well as IL8RBP, a pseudogene of IL8RB, form a gene cluster in a region mapped to chromosome 2q33-q36. [provided by RefSeq, Jul 2008]","start":218162845,"end":218166995,"strand":-1,"description":"C-X-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:6026]"}, {"versioned_ensembl_gene_id":"ENSG00000251405.2","gene_symbol":"AC008676.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":157362615,"end":157460078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205955.4","gene_symbol":"HSP90AA5P","gene_name":"heat shock protein 90 alpha family class A member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32535]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"730211","summary":null,"start":184115352,"end":184117898,"strand":1,"description":"heat shock protein 90 alpha family class A member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32535]"}, {"versioned_ensembl_gene_id":"ENSG00000256640.1","gene_symbol":"AC023051.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26800843,"end":26801302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266924.1","gene_symbol":"AC021594.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79787121,"end":79791432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255750.5","gene_symbol":"AC022509.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26230819,"end":26319720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259207.7","gene_symbol":"ITGB3","gene_name":"integrin subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:6156]","synonyms":"GPIIIa,GP3A,CD61","biotype":"protein_coding","ncbi_id":"3690","summary":"The ITGB3 protein product is the integrin beta chain beta 3. Integrins are integral cell-surface proteins composed of an alpha chain and a beta chain. A given chain may combine with multiple partners resulting in different integrins. Integrin beta 3 is found along with the alpha IIb chain in platelets. Integrins are known to participate in cell adhesion as well as cell-surface mediated signalling. [provided by RefSeq, Jul 2008]","start":47253846,"end":47311816,"strand":1,"description":"integrin subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:6156]"}, {"versioned_ensembl_gene_id":"ENSG00000249915.7","gene_symbol":"PDCD6","gene_name":"programmed cell death 6 [Source:HGNC Symbol;Acc:HGNC:8765]","synonyms":"PEF1B,ALG-2","biotype":"protein_coding","ncbi_id":"10016","summary":"This gene encodes a calcium-binding protein belonging to the penta-EF-hand protein family. Calcium binding is important for homodimerization and for conformational changes required for binding to other protein partners. This gene product participates in T cell receptor-, Fas-, and glucocorticoid-induced programmed cell death. In mice deficient for this gene product, however, apoptosis was not blocked suggesting this gene product is functionally redundant. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is also located on the short arm of chromosome 5. [provided by RefSeq, May 2012]","start":271621,"end":353856,"strand":1,"description":"programmed cell death 6 [Source:HGNC Symbol;Acc:HGNC:8765]"}, {"versioned_ensembl_gene_id":"ENSG00000164089.8","gene_symbol":"ETNPPL","gene_name":"ethanolamine-phosphate phospho-lyase [Source:HGNC Symbol;Acc:HGNC:14404]","synonyms":"AGXT2L1","biotype":"protein_coding","ncbi_id":"64850","summary":null,"start":108742040,"end":108763054,"strand":-1,"description":"ethanolamine-phosphate phospho-lyase [Source:HGNC Symbol;Acc:HGNC:14404]"}, {"versioned_ensembl_gene_id":"ENSG00000262786.1","gene_symbol":"AC005224.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14295512,"end":14297600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146476.10","gene_symbol":"ARMT1","gene_name":"acidic residue methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17872]","synonyms":"FLJ12910,C6orf211","biotype":"protein_coding","ncbi_id":"79624","summary":null,"start":151452258,"end":151470101,"strand":1,"description":"acidic residue methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:17872]"}, {"versioned_ensembl_gene_id":"ENSG00000280207.1","gene_symbol":"AC106795.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177967004,"end":177967457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254680.1","gene_symbol":"AC079329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12261426,"end":12263173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259315.1","gene_symbol":"ACTG1P17","gene_name":"actin gamma 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51497]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"283693","summary":null,"start":82725873,"end":82738904,"strand":-1,"description":"actin gamma 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51497]"}, {"versioned_ensembl_gene_id":"ENSG00000281778.1","gene_symbol":"LINC00550","gene_name":"long intergenic non-protein coding RNA 550 [Source:HGNC Symbol;Acc:HGNC:43688]","synonyms":null,"biotype":"lincRNA","ncbi_id":"338862","summary":null,"start":68861284,"end":68885325,"strand":-1,"description":"long intergenic non-protein coding RNA 550 [Source:HGNC Symbol;Acc:HGNC:43688]"}, {"versioned_ensembl_gene_id":"ENSG00000229824.1","gene_symbol":"RPL12P34","gene_name":"ribosomal protein L12 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36168]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271407","summary":null,"start":68654572,"end":68655050,"strand":1,"description":"ribosomal protein L12 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36168]"}, {"versioned_ensembl_gene_id":"ENSG00000124157.6","gene_symbol":"SEMG2","gene_name":"semenogelin II [Source:HGNC Symbol;Acc:HGNC:10743]","synonyms":"SGII","biotype":"protein_coding","ncbi_id":"6407","summary":"The secreted protein encoded by this gene is involved in the formation of a gel matrix that encases ejaculated spermatozoa. Proteolysis by the prostate-specific antigen (PSA) breaks down the gel matrix and allows the spermatozoa to move more freely. The encoded protein is found in lesser abundance than a similar semenogelin protein. An antibacterial activity has been found for a antimicrobial peptide isolated from this protein. The genes encoding these two semenogelin proteins are found in a cluster on chromosome 20. [provided by RefSeq, Jan 2015]","start":45221300,"end":45224458,"strand":1,"description":"semenogelin II [Source:HGNC Symbol;Acc:HGNC:10743]"}, {"versioned_ensembl_gene_id":"ENSG00000184954.4","gene_symbol":"OR6C70","gene_name":"olfactory receptor family 6 subfamily C member 70 [Source:HGNC Symbol;Acc:HGNC:31299]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390327","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":55469200,"end":55470138,"strand":-1,"description":"olfactory receptor family 6 subfamily C member 70 [Source:HGNC Symbol;Acc:HGNC:31299]"}, {"versioned_ensembl_gene_id":"ENSG00000255400.1","gene_symbol":"AC124276.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12086891,"end":12089441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281161.1","gene_symbol":"BX927359.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104596165,"end":104596991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275463.4","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"LIR-2,MIR10,ILT4,MIR-10,CD85d,LIR2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54274422,"end":54281786,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000213601.3","gene_symbol":"KRT18P19","gene_name":"keratin 18 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33387]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339781","summary":null,"start":189311263,"end":189311967,"strand":-1,"description":"keratin 18 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:33387]"}, {"versioned_ensembl_gene_id":"ENSG00000274126.4","gene_symbol":"C14orf180","gene_name":"chromosome 14 open reading frame 180 [Source:HGNC Symbol;Acc:HGNC:33795]","synonyms":"NRAC,C14orf77","biotype":"protein_coding","ncbi_id":"400258","summary":null,"start":104586828,"end":104597659,"strand":1,"description":"chromosome 14 open reading frame 180 [Source:HGNC Symbol;Acc:HGNC:33795]"}, {"versioned_ensembl_gene_id":"ENSG00000214146.2","gene_symbol":"LINC02026","gene_name":"long intergenic non-protein coding RNA 2026 [Source:HGNC Symbol;Acc:HGNC:52861]","synonyms":null,"biotype":"lincRNA","ncbi_id":"647323","summary":null,"start":193957372,"end":194003659,"strand":-1,"description":"long intergenic non-protein coding RNA 2026 [Source:HGNC Symbol;Acc:HGNC:52861]"}, {"versioned_ensembl_gene_id":"ENSG00000117862.11","gene_symbol":"TXNDC12","gene_name":"thioredoxin domain containing 12 [Source:HGNC Symbol;Acc:HGNC:24626]","synonyms":"AGR1,TLP19,PDIA16,hAG-1,ERP19,ERP18","biotype":"protein_coding","ncbi_id":"51060","summary":"This gene encodes a member of the thioredoxin superfamily. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. This protein localizes to the endoplasmic reticulum and has a single atypical active motif. The encoded protein is mainly involved in catalyzing native disulfide bond formation and displays activity similar to protein-disulfide isomerases. This protein may play a role in defense against endoplasmic reticulum stress. Alternate splicing results in both coding and non-coding variants. [provided by RefSeq, Mar 2012]","start":52020131,"end":52056171,"strand":-1,"description":"thioredoxin domain containing 12 [Source:HGNC Symbol;Acc:HGNC:24626]"}, {"versioned_ensembl_gene_id":"ENSG00000178776.4","gene_symbol":"C5orf46","gene_name":"chromosome 5 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:33768]","synonyms":"SSSP1,MGC23985","biotype":"protein_coding","ncbi_id":"389336","summary":null,"start":147880726,"end":147906538,"strand":-1,"description":"chromosome 5 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:33768]"}, {"versioned_ensembl_gene_id":"ENSG00000047365.11","gene_symbol":"ARAP2","gene_name":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:16924]","synonyms":"PARX,CENTD1","biotype":"protein_coding","ncbi_id":"116984","summary":"The protein encoded by this gene contains ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology domains. The protein is a phosphatidylinositol (3,4,5)-trisphosphate-dependent Arf6 GAP that binds RhoA-GTP, but it lacks the predicted catalytic arginine in the RHO-GAP domain and does not have RHO-GAP activity. The protein associates with focal adhesions and functions downstream of RhoA to regulate focal adhesion dynamics. [provided by RefSeq, Sep 2008]","start":35948221,"end":36244509,"strand":-1,"description":"ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:HGNC:16924]"}, {"versioned_ensembl_gene_id":"ENSG00000163293.11","gene_symbol":"NIPAL1","gene_name":"NIPA like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27194]","synonyms":"NPAL1,DKFZp686A06115","biotype":"protein_coding","ncbi_id":"152519","summary":null,"start":47914142,"end":48040173,"strand":1,"description":"NIPA like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27194]"}, {"versioned_ensembl_gene_id":"ENSG00000222005.8","gene_symbol":"LINC01118","gene_name":"long intergenic non-protein coding RNA 1118 [Source:HGNC Symbol;Acc:HGNC:49261]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388948","summary":null,"start":46816668,"end":46822657,"strand":1,"description":"long intergenic non-protein coding RNA 1118 [Source:HGNC Symbol;Acc:HGNC:49261]"}, {"versioned_ensembl_gene_id":"ENSG00000131885.16","gene_symbol":"KRT17P1","gene_name":"keratin 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6428]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"147228","summary":null,"start":16840743,"end":16845883,"strand":-1,"description":"keratin 17 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6428]"}, {"versioned_ensembl_gene_id":"ENSG00000223986.1","gene_symbol":"AC069421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":193765681,"end":193766003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280032.1","gene_symbol":"AP002800.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":118264593,"end":118266817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224916.9","gene_symbol":"APOC4-APOC2","gene_name":"APOC4-APOC2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44426]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533990","summary":"This locus represents naturally occurring read-through transcription between the neighboring apolipoprotein C-IV (APOC4) and apolipoprotein C-II (APOC2) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":44942238,"end":44949565,"strand":1,"description":"APOC4-APOC2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44426]"}, {"versioned_ensembl_gene_id":"ENSG00000255338.1","gene_symbol":"AC118273.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49110756,"end":49111220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274023.1","gene_symbol":"AL360169.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":158282841,"end":158428379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254412.1","gene_symbol":"AC118273.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49098163,"end":49101168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263531.1","gene_symbol":"AC130324.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30863921,"end":30864940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218490.1","gene_symbol":"FCF1P10","gene_name":"FCF1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:44622]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479046","summary":null,"start":113010937,"end":113011415,"strand":1,"description":"FCF1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:44622]"}, {"versioned_ensembl_gene_id":"ENSG00000136928.6","gene_symbol":"GABBR2","gene_name":"gamma-aminobutyric acid type B receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:4507]","synonyms":"HG20,GPRC3B,GPR51,GABABR2","biotype":"protein_coding","ncbi_id":"9568","summary":"The multi-pass membrane protein encoded by this gene belongs to the G-protein coupled receptor 3 family and GABA-B receptor subfamily. The GABA-B receptors inhibit neuronal activity through G protein-coupled second-messenger systems, which regulate the release of neurotransmitters, and the activity of ion channels and adenylyl cyclase. This receptor subunit forms an active heterodimeric complex with GABA-B receptor subunit 1, neither of which is effective on its own. Allelic variants of this gene have been associated with nicotine dependence.[provided by RefSeq, Jan 2010]","start":98288082,"end":98709197,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:4507]"}, {"versioned_ensembl_gene_id":"ENSG00000233840.1","gene_symbol":"PCDH9-AS4","gene_name":"PCDH9 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40428]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874087","summary":null,"start":66990886,"end":67002007,"strand":1,"description":"PCDH9 antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40428]"}, {"versioned_ensembl_gene_id":"ENSG00000276637.1","gene_symbol":"AC084851.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49067610,"end":49069301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251294.1","gene_symbol":"AC091885.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24554018,"end":24613222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166997.7","gene_symbol":"CNPY4","gene_name":"canopy FGF signaling regulator 4 [Source:HGNC Symbol;Acc:HGNC:28631]","synonyms":"PRAT4B,MGC40499","biotype":"protein_coding","ncbi_id":"245812","summary":null,"start":100119613,"end":100125511,"strand":1,"description":"canopy FGF signaling regulator 4 [Source:HGNC Symbol;Acc:HGNC:28631]"}, {"versioned_ensembl_gene_id":"ENSG00000230338.1","gene_symbol":"MTND4P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42206]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873351","summary":null,"start":94774156,"end":94774633,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42206]"}, {"versioned_ensembl_gene_id":"ENSG00000175175.5","gene_symbol":"PPM1E","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1E [Source:HGNC Symbol;Acc:HGNC:19322]","synonyms":"POPX1,KIAA1072,CaMKP-N,PP2CH","biotype":"protein_coding","ncbi_id":"22843","summary":"This gene encodes a member of the PPM family of serine/threonine-protein phosphatases. The encoded protein is localized to the nucleus and dephosphorylates and inactivates multiple substrates including serine/threonine-protein kinase PAK 1, 5'-AMP-activated protein kinase (AMPK) and the multifunctional calcium/calmodulin-dependent protein kinases. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2012]","start":58755869,"end":58985176,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1E [Source:HGNC Symbol;Acc:HGNC:19322]"}, {"versioned_ensembl_gene_id":"ENSG00000164049.14","gene_symbol":"FBXW12","gene_name":"F-box and WD repeat domain containing 12 [Source:HGNC Symbol;Acc:HGNC:20729]","synonyms":"FBXO35,Fbw12","biotype":"protein_coding","ncbi_id":"285231","summary":"Members of the F-box protein family, such as FBXW12, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":48372219,"end":48401259,"strand":1,"description":"F-box and WD repeat domain containing 12 [Source:HGNC Symbol;Acc:HGNC:20729]"}, {"versioned_ensembl_gene_id":"ENSG00000108021.19","gene_symbol":"FAM208B","gene_name":"family with sequence similarity 208 member B [Source:HGNC Symbol;Acc:HGNC:23484]","synonyms":"KIAA2006,FLJ20360,C10orf18,bA318E3.2","biotype":"protein_coding","ncbi_id":"54906","summary":null,"start":5684838,"end":5763740,"strand":1,"description":"family with sequence similarity 208 member B [Source:HGNC Symbol;Acc:HGNC:23484]"}, {"versioned_ensembl_gene_id":"ENSG00000230027.1","gene_symbol":"AC092813.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76041691,"end":76066228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187773.8","gene_symbol":"FAM69C","gene_name":"family with sequence similarity 69 member C [Source:HGNC Symbol;Acc:HGNC:31729]","synonyms":"C18orf51","biotype":"protein_coding","ncbi_id":"125704","summary":"This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011]","start":74434099,"end":74457944,"strand":-1,"description":"family with sequence similarity 69 member C [Source:HGNC Symbol;Acc:HGNC:31729]"}, {"versioned_ensembl_gene_id":"ENSG00000225605.2","gene_symbol":"AC092813.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75932479,"end":76019356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236834.1","gene_symbol":"LINC00421","gene_name":"long intergenic non-protein coding RNA 421 [Source:HGNC Symbol;Acc:HGNC:42755]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287114","summary":null,"start":19345049,"end":19346749,"strand":1,"description":"long intergenic non-protein coding RNA 421 [Source:HGNC Symbol;Acc:HGNC:42755]"}, {"versioned_ensembl_gene_id":"ENSG00000279283.1","gene_symbol":"AC131009.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131896500,"end":131898239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224809.2","gene_symbol":"BEND3P2","gene_name":"BEN domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45015]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392368","summary":null,"start":92171241,"end":92173494,"strand":1,"description":"BEN domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45015]"}, {"versioned_ensembl_gene_id":"ENSG00000224506.2","gene_symbol":"LINC02523","gene_name":"long intergenic non-protein coding RNA 2523 [Source:HGNC Symbol;Acc:HGNC:53542]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643623","summary":null,"start":125674353,"end":125720218,"strand":1,"description":"long intergenic non-protein coding RNA 2523 [Source:HGNC Symbol;Acc:HGNC:53542]"}, {"versioned_ensembl_gene_id":"ENSG00000225358.1","gene_symbol":"MIPEPP1","gene_name":"mitochondrial intermediate peptidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533682","summary":null,"start":112735166,"end":112738693,"strand":-1,"description":"mitochondrial intermediate peptidase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39456]"}, {"versioned_ensembl_gene_id":"ENSG00000224056.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31168631,"end":31172797,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000238020.1","gene_symbol":"HTR3E-AS1","gene_name":"HTR3E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41032]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478970","summary":null,"start":184095118,"end":184105178,"strand":-1,"description":"HTR3E antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41032]"}, {"versioned_ensembl_gene_id":"ENSG00000236257.1","gene_symbol":"EI24P2","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44587]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129866","summary":null,"start":158454198,"end":158455273,"strand":1,"description":"EI24, autophagy associated transmembrane protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44587]"}, {"versioned_ensembl_gene_id":"ENSG00000248591.1","gene_symbol":"AC109445.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23456468,"end":23456850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196923.13","gene_symbol":"PDLIM7","gene_name":"PDZ and LIM domain 7 [Source:HGNC Symbol;Acc:HGNC:22958]","synonyms":"ENIGMA","biotype":"protein_coding","ncbi_id":"9260","summary":"The protein encoded by this gene is representative of a family of proteins composed of conserved PDZ and LIM domains. LIM domains are proposed to function in protein-protein recognition in a variety of contexts including gene transcription and development and in cytoskeletal interaction. The LIM domains of this protein bind to protein kinases, whereas the PDZ domain binds to actin filaments. The gene product is involved in the assembly of an actin filament-associated complex essential for transmission of ret/ptc2 mitogenic signaling. The biological function is likely to be that of an adapter, with the PDZ domain localizing the LIM-binding proteins to actin filaments of both skeletal muscle and nonmuscle tissues. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":177483394,"end":177497606,"strand":-1,"description":"PDZ and LIM domain 7 [Source:HGNC Symbol;Acc:HGNC:22958]"}, {"versioned_ensembl_gene_id":"ENSG00000233054.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR2B3P,OR6-4","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086337,"end":29087343,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000250319.1","gene_symbol":"AC010460.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23262159,"end":23263185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236070.1","gene_symbol":"CR759957.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026712,"end":29027639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242593.5","gene_symbol":"AC006148.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":124032205,"end":124395118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089289.15","gene_symbol":"IGBP1","gene_name":"immunoglobulin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5461]","synonyms":"IBP1","biotype":"protein_coding","ncbi_id":"3476","summary":"The proliferation and differentiation of B cells is dependent upon a B-cell antigen receptor (BCR) complex. Binding of antigens to specific B-cell receptors results in a tyrosine phosphorylation reaction through the BCR complex and leads to multiple signal transduction pathways. [provided by RefSeq, Jul 2008]","start":70133449,"end":70166324,"strand":1,"description":"immunoglobulin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:5461]"}, {"versioned_ensembl_gene_id":"ENSG00000220925.2","gene_symbol":"IGBP1-AS2","gene_name":"IGBP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40294]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478965","summary":null,"start":70148582,"end":70149654,"strand":-1,"description":"IGBP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40294]"}, {"versioned_ensembl_gene_id":"ENSG00000250249.2","gene_symbol":"AC105313.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62291562,"end":62292337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278096.1","gene_symbol":"AC142525.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":69477193,"end":69502181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223646.1","gene_symbol":"AC002463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112622378,"end":112708080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226007.2","gene_symbol":"BX005266.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62532337,"end":62534724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259489.2","gene_symbol":"KRT18P47","gene_name":"keratin 18 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:33417]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390634","summary":null,"start":88960070,"end":88961046,"strand":1,"description":"keratin 18 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:33417]"}, {"versioned_ensembl_gene_id":"ENSG00000270194.1","gene_symbol":"AC097359.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37241789,"end":37244177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232348.2","gene_symbol":"LINC00279","gene_name":"long intergenic non-protein coding RNA 279 [Source:HGNC Symbol;Acc:HGNC:38724]","synonyms":"NCRNA00279","biotype":"lincRNA","ncbi_id":"100873963","summary":null,"start":8638294,"end":8644842,"strand":1,"description":"long intergenic non-protein coding RNA 279 [Source:HGNC Symbol;Acc:HGNC:38724]"}, {"versioned_ensembl_gene_id":"ENSG00000177984.6","gene_symbol":"LCN15","gene_name":"lipocalin 15 [Source:HGNC Symbol;Acc:HGNC:33777]","synonyms":"UNQ2541,PRO6093","biotype":"protein_coding","ncbi_id":"389812","summary":null,"start":136759634,"end":136766255,"strand":-1,"description":"lipocalin 15 [Source:HGNC Symbol;Acc:HGNC:33777]"}, {"versioned_ensembl_gene_id":"ENSG00000167653.4","gene_symbol":"PSCA","gene_name":"prostate stem cell antigen [Source:HGNC Symbol;Acc:HGNC:9500]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8000","summary":"This gene encodes a glycosylphosphatidylinositol-anchored cell membrane glycoprotein. In addition to being highly expressed in the prostate it is also expressed in the bladder, placenta, colon, kidney, and stomach. This gene is up-regulated in a large proportion of prostate cancers and is also detected in cancers of the bladder and pancreas. This gene includes a polymorphism that results in an upstream start codon in some individuals; this polymorphism is thought to be associated with a risk for certain gastric and bladder cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":142670308,"end":142682724,"strand":1,"description":"prostate stem cell antigen [Source:HGNC Symbol;Acc:HGNC:9500]"}, {"versioned_ensembl_gene_id":"ENSG00000126882.12","gene_symbol":"FAM78A","gene_name":"family with sequence similarity 78 member A [Source:HGNC Symbol;Acc:HGNC:25465]","synonyms":"FLJ00024,C9orf59","biotype":"protein_coding","ncbi_id":"286336","summary":null,"start":131258076,"end":131276547,"strand":-1,"description":"family with sequence similarity 78 member A [Source:HGNC Symbol;Acc:HGNC:25465]"}, {"versioned_ensembl_gene_id":"ENSG00000281821.1","gene_symbol":"AC233280.17","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195639990,"end":195640460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261044.1","gene_symbol":"AP006547.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142620373,"end":142621064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251129.1","gene_symbol":"LINC02506","gene_name":"long intergenic non-protein coding RNA 2506 [Source:HGNC Symbol;Acc:HGNC:53495]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723828","summary":null,"start":31997397,"end":32155406,"strand":1,"description":"long intergenic non-protein coding RNA 2506 [Source:HGNC Symbol;Acc:HGNC:53495]"}, {"versioned_ensembl_gene_id":"ENSG00000223511.6","gene_symbol":"AL683807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1732584,"end":1755985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229725.1","gene_symbol":"AC007322.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21871331,"end":21873550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272906.1","gene_symbol":"AL353708.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179881607,"end":179882595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196302.5","gene_symbol":"AC146944.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70516387,"end":70555266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198598.6","gene_symbol":"MMP17","gene_name":"matrix metallopeptidase 17 [Source:HGNC Symbol;Acc:HGNC:7163]","synonyms":"MT4-MMP","biotype":"protein_coding","ncbi_id":"4326","summary":"This gene encodes a member of the peptidase M10 family and membrane-type subfamily of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Members of this subfamily contain a transmembrane domain suggesting that these proteins are expressed at the cell surface rather than secreted. The encoded preproprotein is proteolytically processed to generate the mature protease. This protein is unique among the membrane-type matrix metalloproteinases in that it is anchored to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor. Elevated expression of the encoded protein has been observed in osteoarthritis and multiple human cancers. [provided by RefSeq, Jan 2016]","start":131828393,"end":131851783,"strand":1,"description":"matrix metallopeptidase 17 [Source:HGNC Symbol;Acc:HGNC:7163]"}, {"versioned_ensembl_gene_id":"ENSG00000254717.2","gene_symbol":"GLYATL1P2","gene_name":"glycine-N-acyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37863]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100129933","summary":null,"start":58878302,"end":58893460,"strand":1,"description":"glycine-N-acyltransferase like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37863]"}, {"versioned_ensembl_gene_id":"ENSG00000281836.1","gene_symbol":"AC136352.11","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21298216,"end":21325353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169905.12","gene_symbol":"TOR1AIP2","gene_name":"torsin 1A interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:24055]","synonyms":"LULL1,IFRG15,NET9","biotype":"protein_coding","ncbi_id":"163590","summary":"One of the two protein isoforms encoded by this gene is a type II integral membrane protein found in the endoplasmic reticulum (ER). The encoded protein is a cofactor for the ATPase TorsinA, regulating the amount of TorsinA present in the ER compared to that found in the nuclear envelope. Defects in this protein are a cause of early onset primary dystonia, a neuromuscular disease. The other isoform encoded by this gene is an interferon alpha responsive protein whose cellular role has yet to be determined. [provided by RefSeq, Mar 2017]","start":179839967,"end":179877803,"strand":-1,"description":"torsin 1A interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:24055]"}, {"versioned_ensembl_gene_id":"ENSG00000111728.10","gene_symbol":"ST8SIA1","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10869]","synonyms":"SIAT8A,SIAT8","biotype":"protein_coding","ncbi_id":"6489","summary":"Gangliosides are membrane-bound glycosphingolipids containing sialic acid. Ganglioside GD3 is known to be important for cell adhesion and growth of cultured malignant cells. The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to GM3 to produce gangliosides GD3 and GT3. The encoded protein may be found in the Golgi apparatus and is a member of glycosyltransferase family 29. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2015]","start":22063773,"end":22437041,"strand":-1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10869]"}, {"versioned_ensembl_gene_id":"ENSG00000284471.1","gene_symbol":"CR769775.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61982796,"end":61986934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181562.4","gene_symbol":"EDDM3A","gene_name":"epididymal protein 3A [Source:HGNC Symbol;Acc:HGNC:16978]","synonyms":"HE3-ALPHA,FAM12A","biotype":"protein_coding","ncbi_id":"10876","summary":"Testicular sperm are morphologically differentiated but are not progressively motile nor able to fertilize an egg. Post-testicular maturation requires exposure of spermatozoa to the microenvironment of the epididymal lumen. Spermatozoa undergo extensive changes in the epididymis, including enzymatic modifications, loss of pre-existing components and addition of new glycoproteins from epididymal secretions. These modifying proteins and enzymes are synthesized by epithelial cells lining the epididymal duct and secreted apically into the lumen, where they come into contact with, and may be absorbed onto, the sperm membranes. The proteins encoded by the genes in this cluster are synthesized and secreted by epididymal epithelial cells. [provided by RefSeq, Jul 2008]","start":20745892,"end":20748380,"strand":1,"description":"epididymal protein 3A [Source:HGNC Symbol;Acc:HGNC:16978]"}, {"versioned_ensembl_gene_id":"ENSG00000284608.1","gene_symbol":"AC016912.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46429195,"end":46484424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112186.11","gene_symbol":"CAP2","gene_name":"cyclase associated actin cytoskeleton regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:20039]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10486","summary":"This gene was identified by its similarity to the gene for human adenylyl cyclase-associated protein. The function of the protein encoded by this gene is unknown. However, the protein appears to be able to interact with adenylyl cyclase-associated protein and actin. [provided by RefSeq, Jul 2008]","start":17393216,"end":17557792,"strand":1,"description":"cyclase associated actin cytoskeleton regulatory protein 2 [Source:HGNC Symbol;Acc:HGNC:20039]"}, {"versioned_ensembl_gene_id":"ENSG00000229956.10","gene_symbol":"ZRANB2-AS2","gene_name":"ZRANB2 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43595]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100852410","summary":null,"start":71081324,"end":71489976,"strand":1,"description":"ZRANB2 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43595]"}, {"versioned_ensembl_gene_id":"ENSG00000171004.18","gene_symbol":"HS6ST2","gene_name":"heparan sulfate 6-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:19133]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90161","summary":"Heparan sulfate proteoglycans are ubiquitous components of the cell surface, extracellular matrix, and basement membranes, and interact with various ligands to influence cell growth, differentiation, adhesion, and migration. This gene encodes a member of the heparan sulfate (HS) sulfotransferase gene family, which catalyze the transfer of sulfate to HS. Different family members and isoforms are thought to synthesize heparan sulfates with tissue-specific structures and functions. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":132626016,"end":132961395,"strand":-1,"description":"heparan sulfate 6-O-sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:19133]"}, {"versioned_ensembl_gene_id":"ENSG00000155918.7","gene_symbol":"RAET1L","gene_name":"retinoic acid early transcript 1L [Source:HGNC Symbol;Acc:HGNC:16798]","synonyms":null,"biotype":"protein_coding","ncbi_id":"154064","summary":"RAET1L belongs to the RAET1 family of major histocompatibility complex (MHC) class I-related genes, which are located within a 180-kb cluster on chromosome 6q24.2-q25.3. The REAT1 genes encode glycoproteins that contain extracellular alpha-1 and alpha-2 domains, but they lack the membrane proximal Ig-like alpha-3 domain. Most RAET1 glycoproteins are anchored to the membrane via glycosylphosphatidylinositol (GPI) linkage (Radosavljevic et al., 2002 [PubMed 11827464]).[supplied by OMIM, Mar 2008]","start":150018334,"end":150025532,"strand":-1,"description":"retinoic acid early transcript 1L [Source:HGNC Symbol;Acc:HGNC:16798]"}, {"versioned_ensembl_gene_id":"ENSG00000253227.1","gene_symbol":"AC090192.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124271683,"end":124277584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225312.2","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"FABGL,SDR30C1,HKE6,D6S2245E,RING2,H2-KE6,KE6","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33182548,"end":33184737,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000230241.1","gene_symbol":"AC244636.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48135658,"end":48136159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227707.1","gene_symbol":"SDAD1P3","gene_name":"SDA1 domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39260]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873858","summary":null,"start":33771963,"end":33772295,"strand":1,"description":"SDA1 domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39260]"}, {"versioned_ensembl_gene_id":"ENSG00000186453.12","gene_symbol":"FAM228A","gene_name":"family with sequence similarity 228 member A [Source:HGNC Symbol;Acc:HGNC:34418]","synonyms":"FLJ30851,C2orf84","biotype":"protein_coding","ncbi_id":"653140","summary":null,"start":24175069,"end":24200849,"strand":1,"description":"family with sequence similarity 228 member A [Source:HGNC Symbol;Acc:HGNC:34418]"}, {"versioned_ensembl_gene_id":"ENSG00000228035.1","gene_symbol":"AL512638.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115283034,"end":115368072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223754.1","gene_symbol":"AC008073.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24199839,"end":24201698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182185.18","gene_symbol":"RAD51B","gene_name":"RAD51 paralog B [Source:HGNC Symbol;Acc:HGNC:9822]","synonyms":"RAD51L1,R51H2,hREC2,REC2","biotype":"protein_coding","ncbi_id":"5890","summary":"The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are evolutionarily conserved proteins essential for DNA repair by homologous recombination. This protein has been shown to form a stable heterodimer with the family member RAD51C, which further interacts with the other family members, such as RAD51, XRCC2, and XRCC3. Overexpression of this gene was found to cause cell cycle G1 delay and cell apoptosis, which suggested a role of this protein in sensing DNA damage. Rearrangements between this locus and high mobility group AT-hook 2 (HMGA2, GeneID 8091) have been observed in uterine leiomyomata. [provided by RefSeq, Mar 2016]","start":67819779,"end":68730218,"strand":1,"description":"RAD51 paralog B [Source:HGNC Symbol;Acc:HGNC:9822]"}, {"versioned_ensembl_gene_id":"ENSG00000248160.1","gene_symbol":"AC233724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17647712,"end":17647944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165671.19","gene_symbol":"NSD1","gene_name":"nuclear receptor binding SET domain protein 1 [Source:HGNC Symbol;Acc:HGNC:14234]","synonyms":"STO,KMT3B,FLJ22263,ARA267","biotype":"protein_coding","ncbi_id":"64324","summary":"This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Sep 2018]","start":177133025,"end":177300215,"strand":1,"description":"nuclear receptor binding SET domain protein 1 [Source:HGNC Symbol;Acc:HGNC:14234]"}, {"versioned_ensembl_gene_id":"ENSG00000196776.14","gene_symbol":"CD47","gene_name":"CD47 molecule [Source:HGNC Symbol;Acc:HGNC:1682]","synonyms":"OA3,MER6,IAP","biotype":"protein_coding","ncbi_id":"961","summary":"This gene encodes a membrane protein, which is involved in the increase in intracellular calcium concentration that occurs upon cell adhesion to extracellular matrix. The encoded protein is also a receptor for the C-terminal cell binding domain of thrombospondin, and it may play a role in membrane transport and signal transduction. This gene has broad tissue distribution, and is reduced in expression on Rh erythrocytes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2010]","start":108043298,"end":108091025,"strand":-1,"description":"CD47 molecule [Source:HGNC Symbol;Acc:HGNC:1682]"}, {"versioned_ensembl_gene_id":"ENSG00000127947.15","gene_symbol":"PTPN12","gene_name":"protein tyrosine phosphatase, non-receptor type 12 [Source:HGNC Symbol;Acc:HGNC:9645]","synonyms":"PTPG1,PTP-PEST","biotype":"protein_coding","ncbi_id":"5782","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains a C-terminal PEST motif, which serves as a protein-protein interaction domain, and may regulate protein intracellular half-life. This PTP was found to bind and dephosphorylate the product of the oncogene c-ABL and thus may play a role in oncogenesis. This PTP was also shown to interact with, and dephosphorylate, various products related to cytoskeletal structure and cell adhesion, such as p130 (Cas), CAKbeta/PTK2B, PSTPIP1, and paxillin. This suggests it has a regulatory role in controlling cell shape and mobility. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":77537275,"end":77640071,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 12 [Source:HGNC Symbol;Acc:HGNC:9645]"}, {"versioned_ensembl_gene_id":"ENSG00000114770.16","gene_symbol":"ABCC5","gene_name":"ATP binding cassette subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:56]","synonyms":"SMRP,MRP5,MOAT-C,EST277145","biotype":"protein_coding","ncbi_id":"10057","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions in the cellular export of its substrate, cyclic nucleotides. This export contributes to the degradation of phosphodiesterases and possibly an elimination pathway for cyclic nucleotides. Studies show that this protein provides resistance to thiopurine anticancer drugs, 6-mercatopurine and thioguanine, and the anti-HIV drug 9-(2-phosphonylmethoxyethyl)adenine. This protein may be involved in resistance to thiopurines in acute lymphoblastic leukemia and antiretroviral nucleoside analogs in HIV-infected patients. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":183919934,"end":184018015,"strand":-1,"description":"ATP binding cassette subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:56]"}, {"versioned_ensembl_gene_id":"ENSG00000229051.1","gene_symbol":"LINC01788","gene_name":"long intergenic non-protein coding RNA 1788 [Source:HGNC Symbol;Acc:HGNC:52577]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927244","summary":null,"start":70706453,"end":70786468,"strand":1,"description":"long intergenic non-protein coding RNA 1788 [Source:HGNC Symbol;Acc:HGNC:52577]"}, {"versioned_ensembl_gene_id":"ENSG00000239882.7","gene_symbol":"CYP21A1P","gene_name":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]","synonyms":"CYP21A,P450c21A,CYP21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1590","summary":null,"start":31998290,"end":32001104,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:2599]"}, {"versioned_ensembl_gene_id":"ENSG00000162971.10","gene_symbol":"TYW5","gene_name":"tRNA-yW synthesizing protein 5 [Source:HGNC Symbol;Acc:HGNC:26754]","synonyms":"FLJ37953,C2orf60","biotype":"protein_coding","ncbi_id":"129450","summary":null,"start":199929975,"end":199955736,"strand":-1,"description":"tRNA-yW synthesizing protein 5 [Source:HGNC Symbol;Acc:HGNC:26754]"}, {"versioned_ensembl_gene_id":"ENSG00000234328.2","gene_symbol":"TNXA","gene_name":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]","synonyms":"TNX,HXBL,D6S103E,XA","biotype":"unprocessed_pseudogene","ncbi_id":"7146","summary":null,"start":32001268,"end":32005126,"strand":-1,"description":"tenascin XA (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11975]"}, {"versioned_ensembl_gene_id":"ENSG00000253875.1","gene_symbol":"AC013643.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27733338,"end":27756426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259953.1","gene_symbol":"AL138756.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":112032555,"end":112037730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223882.1","gene_symbol":"ABCC5-AS1","gene_name":"ABCC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40055]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873982","summary":null,"start":184006338,"end":184011419,"strand":1,"description":"ABCC5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40055]"}, {"versioned_ensembl_gene_id":"ENSG00000226361.5","gene_symbol":"TERF1P5","gene_name":"telomeric repeat binding factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283523","summary":null,"start":18680494,"end":18681700,"strand":1,"description":"telomeric repeat binding factor 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39686]"}, {"versioned_ensembl_gene_id":"ENSG00000236191.3","gene_symbol":"AC090096.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68525517,"end":68525906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278485.1","gene_symbol":"AL590491.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60944555,"end":60944636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235680.8","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29823861,"end":29828018,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000273478.1","gene_symbol":"AC099676.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":201995696,"end":201996352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258771.1","gene_symbol":"BCAR1P2","gene_name":"breast cancer anti-estrogen resistance 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533718","summary":null,"start":21080812,"end":21081447,"strand":-1,"description":"breast cancer anti-estrogen resistance 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51326]"}, {"versioned_ensembl_gene_id":"ENSG00000259025.1","gene_symbol":"AC037471.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21053004,"end":21054702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259698.1","gene_symbol":"FAM30C","gene_name":"family with sequence similarity 30 member C [Source:HGNC Symbol;Acc:HGNC:31024]","synonyms":"KIAA0125P2,HsT16041","biotype":"unprocessed_pseudogene","ncbi_id":"654499","summary":null,"start":21019388,"end":21020851,"strand":1,"description":"family with sequence similarity 30 member C [Source:HGNC Symbol;Acc:HGNC:31024]"}, {"versioned_ensembl_gene_id":"ENSG00000248471.2","gene_symbol":"AC233724.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17642962,"end":17643228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178700.7","gene_symbol":"DHFR2","gene_name":"dihydrofolate reductase 2 [Source:HGNC Symbol;Acc:HGNC:27309]","synonyms":"FLJ16119,DHFRP4,DHFRL1","biotype":"protein_coding","ncbi_id":"200895","summary":null,"start":94047836,"end":94063389,"strand":-1,"description":"dihydrofolate reductase 2 [Source:HGNC Symbol;Acc:HGNC:27309]"}, {"versioned_ensembl_gene_id":"ENSG00000270531.1","gene_symbol":"AC022001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11529488,"end":11529755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118454.12","gene_symbol":"ANKRD13C","gene_name":"ankyrin repeat domain 13C [Source:HGNC Symbol;Acc:HGNC:25374]","synonyms":"DKFZP566D1346,dJ677H15.3","biotype":"protein_coding","ncbi_id":"81573","summary":null,"start":70260588,"end":70354734,"strand":-1,"description":"ankyrin repeat domain 13C [Source:HGNC Symbol;Acc:HGNC:25374]"}, {"versioned_ensembl_gene_id":"ENSG00000158805.11","gene_symbol":"ZNF276","gene_name":"zinc finger protein 276 [Source:HGNC Symbol;Acc:HGNC:23330]","synonyms":"ZNF477,ZFP276,ZADT,MGC45417,CENPZ,CENP-Z","biotype":"protein_coding","ncbi_id":"92822","summary":null,"start":89720400,"end":89740903,"strand":1,"description":"zinc finger protein 276 [Source:HGNC Symbol;Acc:HGNC:23330]"}, {"versioned_ensembl_gene_id":"ENSG00000263396.1","gene_symbol":"AP005119.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1357651,"end":1357942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197961.11","gene_symbol":"ZNF121","gene_name":"zinc finger protein 121 [Source:HGNC Symbol;Acc:HGNC:12904]","synonyms":"ZNF20,ZHC32,D19S204","biotype":"protein_coding","ncbi_id":"7675","summary":null,"start":9560353,"end":9584533,"strand":-1,"description":"zinc finger protein 121 [Source:HGNC Symbol;Acc:HGNC:12904]"}, {"versioned_ensembl_gene_id":"ENSG00000110324.10","gene_symbol":"IL10RA","gene_name":"interleukin 10 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5964]","synonyms":"IL10R,HIL-10R,CDW210A,CD210a,CD210","biotype":"protein_coding","ncbi_id":"3587","summary":"The protein encoded by this gene is a receptor for interleukin 10. This protein is structurally related to interferon receptors. It has been shown to mediate the immunosuppressive signal of interleukin 10, and thus inhibits the synthesis of proinflammatory cytokines. This receptor is reported to promote survival of progenitor myeloid cells through the insulin receptor substrate-2/PI 3-kinase/AKT pathway. Activation of this receptor leads to tyrosine phosphorylation of JAK1 and TYK2 kinases. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Jan 2009]","start":117986348,"end":118003037,"strand":1,"description":"interleukin 10 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:5964]"}, {"versioned_ensembl_gene_id":"ENSG00000180228.12","gene_symbol":"PRKRA","gene_name":"protein activator of interferon induced protein kinase EIF2AK2 [Source:HGNC Symbol;Acc:HGNC:9438]","synonyms":"HSD14,DYT16,RAX,PACT","biotype":"protein_coding","ncbi_id":"8575","summary":"This gene encodes a protein kinase activated by double-stranded RNA which mediates the effects of interferon in response to viral infection. Mutations in this gene have been associated with dystonia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":178431414,"end":178451512,"strand":-1,"description":"protein activator of interferon induced protein kinase EIF2AK2 [Source:HGNC Symbol;Acc:HGNC:9438]"}, {"versioned_ensembl_gene_id":"ENSG00000258855.1","gene_symbol":"OR11J2P","gene_name":"olfactory receptor family 11 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15370]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81110","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":20960675,"end":20961581,"strand":1,"description":"olfactory receptor family 11 subfamily J member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:15370]"}, {"versioned_ensembl_gene_id":"ENSG00000241457.1","gene_symbol":"PLSCR5-AS1","gene_name":"PLSCR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40907]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874104","summary":null,"start":146589602,"end":146590325,"strand":1,"description":"PLSCR5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40907]"}, {"versioned_ensembl_gene_id":"ENSG00000223660.1","gene_symbol":"AC245052.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54199454,"end":54199971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225463.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33215705,"end":33216328,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000239329.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":33088404,"end":33106898,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000278611.1","gene_symbol":"AC008567.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9538733,"end":9539734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278231.1","gene_symbol":"AL133342.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48821688,"end":48849458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069849.10","gene_symbol":"ATP1B3","gene_name":"ATPase Na+/K+ transporting subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:806]","synonyms":"FLJ29027,CD298","biotype":"protein_coding","ncbi_id":"483","summary":"The protein encoded by this gene belongs to the family of Na+/K+ and H+/K+ ATPases beta chain proteins, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The beta subunit regulates, through assembly of alpha/beta heterodimers, the number of sodium pumps transported to the plasma membrane. The glycoprotein subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes a beta 3 subunit. This gene encodes a beta 3 subunit. A pseudogene exists for this gene, and it is located on chromosome 2. [provided by RefSeq, Jul 2008]","start":141876124,"end":141926514,"strand":1,"description":"ATPase Na+/K+ transporting subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:806]"}, {"versioned_ensembl_gene_id":"ENSG00000258552.1","gene_symbol":"AC007375.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77173075,"end":77173652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162510.5","gene_symbol":"MATN1","gene_name":"matrilin 1, cartilage matrix protein [Source:HGNC Symbol;Acc:HGNC:6907]","synonyms":"CRTM,CMP","biotype":"protein_coding","ncbi_id":"4146","summary":"This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias. [provided by RefSeq, Jul 2008]","start":30711277,"end":30723587,"strand":-1,"description":"matrilin 1, cartilage matrix protein [Source:HGNC Symbol;Acc:HGNC:6907]"}, {"versioned_ensembl_gene_id":"ENSG00000241213.1","gene_symbol":"LINC02024","gene_name":"long intergenic non-protein coding RNA 2024 [Source:HGNC Symbol;Acc:HGNC:52859]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374057","summary":null,"start":117678693,"end":117690932,"strand":-1,"description":"long intergenic non-protein coding RNA 2024 [Source:HGNC Symbol;Acc:HGNC:52859]"}, {"versioned_ensembl_gene_id":"ENSG00000234489.1","gene_symbol":"ALDH7A1P4","gene_name":"aldehyde dehydrogenase 7 family member A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:881]","synonyms":"ATQL4","biotype":"processed_pseudogene","ncbi_id":"544","summary":null,"start":62741208,"end":62741385,"strand":-1,"description":"aldehyde dehydrogenase 7 family member A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:881]"}, {"versioned_ensembl_gene_id":"ENSG00000167419.10","gene_symbol":"LPO","gene_name":"lactoperoxidase [Source:HGNC Symbol;Acc:HGNC:6678]","synonyms":"SPO","biotype":"protein_coding","ncbi_id":"4025","summary":"This gene encodes a member of the peroxidase family of proteins. The encoded preproprotein is proteolytically processed to generate the mature enzyme. Following its secretion from salivary, mammary, and other mucosal glands, this enzyme catalyzes the generation of the antimicrobial substance hypothiocyanous acid. This gene is present in a gene cluster on chromosome 17. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":58218548,"end":58268518,"strand":1,"description":"lactoperoxidase [Source:HGNC Symbol;Acc:HGNC:6678]"}, {"versioned_ensembl_gene_id":"ENSG00000072694.20","gene_symbol":"FCGR2B","gene_name":"Fc fragment of IgG receptor IIb [Source:HGNC Symbol;Acc:HGNC:3618]","synonyms":"CD32,FCGR2,FCG2,CD32B","biotype":"protein_coding","ncbi_id":"2213","summary":"The protein encoded by this gene is a low affinity receptor for the Fc region of immunoglobulin gamma complexes. The encoded protein is involved in the phagocytosis of immune complexes and in the regulation of antibody production by B-cells. Variations in this gene may increase susceptibilty to systemic lupus erythematosus (SLE). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":161663147,"end":161678654,"strand":1,"description":"Fc fragment of IgG receptor IIb [Source:HGNC Symbol;Acc:HGNC:3618]"}, {"versioned_ensembl_gene_id":"ENSG00000113621.14","gene_symbol":"TXNDC15","gene_name":"thioredoxin domain containing 15 [Source:HGNC Symbol;Acc:HGNC:20652]","synonyms":"FLJ22625,C5orf14,2310047H23Rik","biotype":"protein_coding","ncbi_id":"79770","summary":"This gene encodes a member of the thioredoxin superfamily. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. [provided by RefSeq, Apr 2017]","start":134873803,"end":134901525,"strand":1,"description":"thioredoxin domain containing 15 [Source:HGNC Symbol;Acc:HGNC:20652]"}, {"versioned_ensembl_gene_id":"ENSG00000266251.1","gene_symbol":"COX6CP3","gene_name":"cytochrome c oxidase subunit 6C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31721]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130247","summary":null,"start":1176790,"end":1177012,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31721]"}, {"versioned_ensembl_gene_id":"ENSG00000249978.1","gene_symbol":"TRGV7","gene_name":"T-cell receptor gamma variable 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12293]","synonyms":"V1S7P,TCRGV7","biotype":"TR_V_pseudogene","ncbi_id":"6981","summary":null,"start":38335041,"end":38335514,"strand":-1,"description":"T-cell receptor gamma variable 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12293]"}, {"versioned_ensembl_gene_id":"ENSG00000140043.11","gene_symbol":"PTGR2","gene_name":"prostaglandin reductase 2 [Source:HGNC Symbol;Acc:HGNC:20149]","synonyms":"FLJ39091,ZADH1","biotype":"protein_coding","ncbi_id":"145482","summary":"This gene encodes an enzyme involved in the metabolism of prostaglandins. The encoded protein catalyzes the NADPH-dependent conversion of 15-keto-prostaglandin E2 to 15-keto-13,14-dihydro-prostaglandin E2. This protein may also be involved in regulating activation of the peroxisome proliferator-activated receptor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":73851844,"end":73886827,"strand":1,"description":"prostaglandin reductase 2 [Source:HGNC Symbol;Acc:HGNC:20149]"}, {"versioned_ensembl_gene_id":"ENSG00000236184.1","gene_symbol":"TCEA1P4","gene_name":"transcription elongation factor A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31091]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421350","summary":null,"start":32979560,"end":32980403,"strand":-1,"description":"transcription elongation factor A1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31091]"}, {"versioned_ensembl_gene_id":"ENSG00000100304.12","gene_symbol":"TTLL12","gene_name":"tubulin tyrosine ligase like 12 [Source:HGNC Symbol;Acc:HGNC:28974]","synonyms":"KIAA0153","biotype":"protein_coding","ncbi_id":"23170","summary":null,"start":43166622,"end":43187133,"strand":-1,"description":"tubulin tyrosine ligase like 12 [Source:HGNC Symbol;Acc:HGNC:28974]"}, {"versioned_ensembl_gene_id":"ENSG00000151491.12","gene_symbol":"EPS8","gene_name":"epidermal growth factor receptor pathway substrate 8 [Source:HGNC Symbol;Acc:HGNC:3420]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2059","summary":"This gene encodes a member of the EPS8 family. This protein contains one PH domain and one SH3 domain. It functions as part of the EGFR pathway, though its exact role has not been determined. Highly similar proteins in other organisms are involved in the transduction of signals from Ras to Rac and growth factor-mediated actin remodeling. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":15620158,"end":15882329,"strand":-1,"description":"epidermal growth factor receptor pathway substrate 8 [Source:HGNC Symbol;Acc:HGNC:3420]"}, {"versioned_ensembl_gene_id":"ENSG00000235292.1","gene_symbol":"AL109838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12243895,"end":12244296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196924.14","gene_symbol":"FLNA","gene_name":"filamin A [Source:HGNC Symbol;Acc:HGNC:3754]","synonyms":"OPD2,OPD1,FLN1,FLN,ABP-280","biotype":"protein_coding","ncbi_id":"2316","summary":"The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]","start":154348524,"end":154374638,"strand":-1,"description":"filamin A [Source:HGNC Symbol;Acc:HGNC:3754]"}, {"versioned_ensembl_gene_id":"ENSG00000270900.1","gene_symbol":"AL360272.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44898711,"end":44899295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224224.1","gene_symbol":"HAUS1P2","gene_name":"HAUS augmin like complex subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43761]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441484","summary":null,"start":18865771,"end":18866554,"strand":1,"description":"HAUS augmin like complex subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43761]"}, {"versioned_ensembl_gene_id":"ENSG00000225783.6","gene_symbol":"MIAT","gene_name":"myocardial infarction associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33425]","synonyms":"NCRNA00066,lncRNA-MIAT,LINC00066,gomafu,FLJ25967,C22orf35,Rncr2","biotype":"lincRNA","ncbi_id":"440823","summary":"This gene encodes a spliced long non-coding RNA that may constitute a component of the nuclear matrix. Altered expression of this locus has been reported to be associated with a susceptibility to myocardial infarction. It has also been proposed that pathways involving this transcript may contribute to the pathophysiology of schizophrenia. A similar gene in mouse has been associated with retinal cell fate determination. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Dec 2014]","start":26646428,"end":26676475,"strand":1,"description":"myocardial infarction associated transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33425]"}, {"versioned_ensembl_gene_id":"ENSG00000206028.1","gene_symbol":"Z99774.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26667693,"end":26672654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229590.3","gene_symbol":"AC005962.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58157028,"end":58157800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279207.1","gene_symbol":"AC015813.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58095672,"end":58101479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216990.2","gene_symbol":"HSPD1P10","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35131]","synonyms":"HSPD1-4P","biotype":"processed_pseudogene","ncbi_id":"644016","summary":null,"start":87298772,"end":87300447,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35131]"}, {"versioned_ensembl_gene_id":"ENSG00000270927.1","gene_symbol":"AL645944.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29904865,"end":29905357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255123.1","gene_symbol":"MTND5P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42296]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873354","summary":null,"start":11239759,"end":11240280,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42296]"}, {"versioned_ensembl_gene_id":"ENSG00000231769.2","gene_symbol":"AL035701.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46097093,"end":46129706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165689.16","gene_symbol":"SDCCAG3","gene_name":"serologically defined colon cancer antigen 3 [Source:HGNC Symbol;Acc:HGNC:10667]","synonyms":"NY-CO-3","biotype":"protein_coding","ncbi_id":"10807","summary":null,"start":136401922,"end":136410609,"strand":-1,"description":"serologically defined colon cancer antigen 3 [Source:HGNC Symbol;Acc:HGNC:10667]"}, {"versioned_ensembl_gene_id":"ENSG00000169093.15","gene_symbol":"ASMTL","gene_name":"acetylserotonin O-methyltransferase like [Source:HGNC Symbol;Acc:HGNC:751]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8623","summary":"The protein encoded by this gene has an N-terminus that is similar to the multicopy associated filamentation (maf) protein of Bacillus subtilis and to orfE of Escherichia coli, while the C-terminus is similar to N-acetylserotonin O-methyltransferase. This gene is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":1403139,"end":1453762,"strand":-1,"description":"acetylserotonin O-methyltransferase like [Source:HGNC Symbol;Acc:HGNC:751]"}, {"versioned_ensembl_gene_id":"ENSG00000137074.18","gene_symbol":"APTX","gene_name":"aprataxin [Source:HGNC Symbol;Acc:HGNC:15984]","synonyms":"FLJ20157,EOAHA,EAOH,AOA1,AXA1,AOA","biotype":"protein_coding","ncbi_id":"54840","summary":"This gene encodes a member of the histidine triad (HIT) superfamily. The encoded protein may play a role in single-stranded DNA repair through its nucleotide-binding activity and its diadenosine polyphosphate hydrolase activity. Mutations in this gene have been associated with ataxia-ocular apraxia. Alternatively spliced transcript variants have been identified for this gene.[provided by RefSeq, Aug 2010]","start":32972606,"end":33025168,"strand":-1,"description":"aprataxin [Source:HGNC Symbol;Acc:HGNC:15984]"}, {"versioned_ensembl_gene_id":"ENSG00000236365.1","gene_symbol":"AL008987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82875649,"end":82875885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270897.1","gene_symbol":"AC111188.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11182107,"end":11182413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261458.1","gene_symbol":"AC009132.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":74842587,"end":74843883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145757.15","gene_symbol":"SPATA9","gene_name":"spermatogenesis associated 9 [Source:HGNC Symbol;Acc:HGNC:22988]","synonyms":"NYD-SP16,FLJ35906","biotype":"protein_coding","ncbi_id":"83890","summary":null,"start":95652181,"end":95698711,"strand":-1,"description":"spermatogenesis associated 9 [Source:HGNC Symbol;Acc:HGNC:22988]"}, {"versioned_ensembl_gene_id":"ENSG00000230311.2","gene_symbol":"TOMM20P4","gene_name":"TOMM20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50522]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129272","summary":null,"start":73223124,"end":73223558,"strand":1,"description":"TOMM20 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50522]"}, {"versioned_ensembl_gene_id":"ENSG00000119725.18","gene_symbol":"ZNF410","gene_name":"zinc finger protein 410 [Source:HGNC Symbol;Acc:HGNC:20144]","synonyms":"APA1,APA-1","biotype":"protein_coding","ncbi_id":"57862","summary":null,"start":73886617,"end":73932511,"strand":1,"description":"zinc finger protein 410 [Source:HGNC Symbol;Acc:HGNC:20144]"}, {"versioned_ensembl_gene_id":"ENSG00000086717.18","gene_symbol":"PPEF1","gene_name":"protein phosphatase with EF-hand domain 1 [Source:HGNC Symbol;Acc:HGNC:9243]","synonyms":"PPP7CA,PPEF","biotype":"protein_coding","ncbi_id":"5475","summary":"This gene encodes a member of the serine/threonine protein phosphatase with EF-hand motif family. The protein contains a protein phosphatase catalytic domain, and at least two EF-hand calcium-binding motifs in its C terminus. Although its substrate(s) is unknown, the encoded protein has been suggested to play a role in specific sensory neuron function and/or development. This gene shares high sequence similarity with the Drosophila retinal degeneration C (rdgC) gene. Several alternatively spliced transcript variants, each encoding a distinct isoform, have been described. [provided by RefSeq, Jul 2008]","start":18675909,"end":18827921,"strand":1,"description":"protein phosphatase with EF-hand domain 1 [Source:HGNC Symbol;Acc:HGNC:9243]"}, {"versioned_ensembl_gene_id":"ENSG00000234837.1","gene_symbol":"AC073464.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94750582,"end":94751293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258414.1","gene_symbol":"AL121790.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37564047,"end":37579125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213816.3","gene_symbol":"CNN2P4","gene_name":"calponin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39529]","synonyms":"CNN2P5","biotype":"processed_pseudogene","ncbi_id":"647507","summary":null,"start":42972386,"end":42973289,"strand":-1,"description":"calponin 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39529]"}, {"versioned_ensembl_gene_id":"ENSG00000259916.1","gene_symbol":"AL845331.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":94588522,"end":94604573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233324.1","gene_symbol":"EEF1A1P34","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:37912]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132358","summary":null,"start":18782424,"end":18783690,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:37912]"}, {"versioned_ensembl_gene_id":"ENSG00000220733.1","gene_symbol":"MTND3P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52166]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075294","summary":null,"start":153668177,"end":153668362,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52166]"}, {"versioned_ensembl_gene_id":"ENSG00000169100.13","gene_symbol":"SLC25A6","gene_name":"solute carrier family 25 member 6 [Source:HGNC Symbol;Acc:HGNC:10992]","synonyms":"MGC17525,ANT3Y,ANT3","biotype":"protein_coding","ncbi_id":"293","summary":"This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein is implicated in the function of the permability transition pore complex (PTPC), which regulates the release of mitochondrial products that induce apoptosis. The human genome contains several non-transcribed pseudogenes of this gene. [provided by RefSeq, Jun 2013]","start":1386152,"end":1392724,"strand":-1,"description":"solute carrier family 25 member 6 [Source:HGNC Symbol;Acc:HGNC:10992]"}, {"versioned_ensembl_gene_id":"ENSG00000272298.1","gene_symbol":"AC091544.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":92699040,"end":92724277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258527.1","gene_symbol":"ASB9P1","gene_name":"ankyrin repeat and SOCS box containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20972]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728619","summary":null,"start":92795647,"end":92796439,"strand":1,"description":"ankyrin repeat and SOCS box containing 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20972]"}, {"versioned_ensembl_gene_id":"ENSG00000280969.1","gene_symbol":"RPS4Y2","gene_name":"ribosomal protein S4, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:18501]","synonyms":"RPS4Y2P","biotype":"protein_coding","ncbi_id":"140032","summary":"The protein encoded by this gene is a ribosomal protein that is highly similar to RPS4Y1. This gene is located in the male-specific region of the Y chromosome. [provided by RefSeq, Aug 2012]","start":20756164,"end":20781032,"strand":1,"description":"ribosomal protein S4, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:18501]"}, {"versioned_ensembl_gene_id":"ENSG00000107859.9","gene_symbol":"PITX3","gene_name":"paired like homeodomain 3 [Source:HGNC Symbol;Acc:HGNC:9006]","synonyms":"ASMD","biotype":"protein_coding","ncbi_id":"5309","summary":"This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family act as transcription factors. This protein is involved in lens formation during eye development. Mutations of this gene have been associated with anterior segment mesenchymal dysgenesis and congenital cataracts. [provided by RefSeq, Jul 2008]","start":102230186,"end":102241474,"strand":-1,"description":"paired like homeodomain 3 [Source:HGNC Symbol;Acc:HGNC:9006]"}, {"versioned_ensembl_gene_id":"ENSG00000260361.1","gene_symbol":"AC106028.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":92779757,"end":92781492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269303.1","gene_symbol":"AC020907.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34998233,"end":35000170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274499.1","gene_symbol":"AC012414.7","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":20803505,"end":20826173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258922.1","gene_symbol":"AC106028.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":92805770,"end":92808567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268533.1","gene_symbol":"AC003002.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57394183,"end":57438457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156515.21","gene_symbol":"HK1","gene_name":"hexokinase 1 [Source:HGNC Symbol;Acc:HGNC:4922]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3098","summary":"Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue-specific. [provided by RefSeq, Apr 2016]","start":69269984,"end":69401882,"strand":1,"description":"hexokinase 1 [Source:HGNC Symbol;Acc:HGNC:4922]"}, {"versioned_ensembl_gene_id":"ENSG00000282596.1","gene_symbol":"DNM1P38","gene_name":"dynamin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35188]","synonyms":"DNM1DN11@,DNM1DN11-8,DNM1DN10@,DNM1DN10-2,DNM1P42","biotype":"unprocessed_pseudogene","ncbi_id":"100216517","summary":null,"start":82610742,"end":82613228,"strand":-1,"description":"dynamin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35188]"}, {"versioned_ensembl_gene_id":"ENSG00000282478.1","gene_symbol":"AL109837.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11536406,"end":11541647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182899.14","gene_symbol":"RPL35A","gene_name":"ribosomal protein L35a [Source:HGNC Symbol;Acc:HGNC:10345]","synonyms":"L35A","biotype":"protein_coding","ncbi_id":"6165","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L35AE family of ribosomal proteins. It is located in the cytoplasm. The rat protein has been shown to bind to both initiator and elongator tRNAs, and thus, it is located at the P site, or P and A sites, of the ribosome. Although this gene was originally mapped to chromosome 18, it has been established that it is located at 3q29-qter. Alternative splicing results in multiple transcript variants. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Oct 2015]","start":197949987,"end":197956610,"strand":1,"description":"ribosomal protein L35a [Source:HGNC Symbol;Acc:HGNC:10345]"}, {"versioned_ensembl_gene_id":"ENSG00000271892.1","gene_symbol":"AC026790.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17107360,"end":17107789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263551.5","gene_symbol":"AP005328.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":976589,"end":1174823,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177096.8","gene_symbol":"FAM109B","gene_name":"family with sequence similarity 109 member B [Source:HGNC Symbol;Acc:HGNC:27161]","synonyms":"SES2,IPIP27B,DKFZp686J07229","biotype":"protein_coding","ncbi_id":"150368","summary":null,"start":42074251,"end":42079441,"strand":1,"description":"family with sequence similarity 109 member B [Source:HGNC Symbol;Acc:HGNC:27161]"}, {"versioned_ensembl_gene_id":"ENSG00000198756.10","gene_symbol":"COLGALT2","gene_name":"collagen beta(1-O)galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16790]","synonyms":"KIAA0584,GLT25D2,C1orf17","biotype":"protein_coding","ncbi_id":"23127","summary":null,"start":183929854,"end":184037729,"strand":-1,"description":"collagen beta(1-O)galactosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16790]"}, {"versioned_ensembl_gene_id":"ENSG00000278446.1","gene_symbol":"AC004852.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9170948,"end":9171273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078579.8","gene_symbol":"FGF20","gene_name":"fibroblast growth factor 20 [Source:HGNC Symbol;Acc:HGNC:3677]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26281","summary":"The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene product is a secreted neurotrophic factor but lacks a typical signal peptide. It is expressed in normal brain, particularly the cerebellum, and may regulate central nervous system development and function. Homodimerization of this protein was shown to regulate its receptor binding activity and concentration gradient in the extracellular matrix. Genetic variations of this gene have been associated with Parkinson disease susceptibility. [provided by RefSeq, Oct 2009]","start":16992169,"end":17002181,"strand":-1,"description":"fibroblast growth factor 20 [Source:HGNC Symbol;Acc:HGNC:3677]"}, {"versioned_ensembl_gene_id":"ENSG00000139974.15","gene_symbol":"SLC38A6","gene_name":"solute carrier family 38 member 6 [Source:HGNC Symbol;Acc:HGNC:19863]","synonyms":"NAT-1","biotype":"protein_coding","ncbi_id":"145389","summary":null,"start":60981114,"end":61083733,"strand":1,"description":"solute carrier family 38 member 6 [Source:HGNC Symbol;Acc:HGNC:19863]"}, {"versioned_ensembl_gene_id":"ENSG00000181374.7","gene_symbol":"CCL13","gene_name":"C-C motif chemokine ligand 13 [Source:HGNC Symbol;Acc:HGNC:10611]","synonyms":"SCYL1,SCYA13,NCC-1,MGC17134,MCP-4,CKb10","biotype":"protein_coding","ncbi_id":"6357","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, lymphocytes, basophils and eosinophils, but not neutrophils. This chemokine plays a role in accumulation of leukocytes during inflammation. It may also be involved in the recruitment of monocytes into the arterial wall during artherosclerosis. [provided by RefSeq, Sep 2014]","start":34356452,"end":34358610,"strand":1,"description":"C-C motif chemokine ligand 13 [Source:HGNC Symbol;Acc:HGNC:10611]"}, {"versioned_ensembl_gene_id":"ENSG00000005882.11","gene_symbol":"PDK2","gene_name":"pyruvate dehydrogenase kinase 2 [Source:HGNC Symbol;Acc:HGNC:8810]","synonyms":"PDHK2","biotype":"protein_coding","ncbi_id":"5164","summary":"This gene encodes a member of the pyruvate dehydrogenase kinase family. The encoded protein phosphorylates pyruvate dehydrogenase, down-regulating the activity of the mitochondrial pyruvate dehydrogenase complex. Overexpression of this gene may play a role in both cancer and diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":50094737,"end":50112152,"strand":1,"description":"pyruvate dehydrogenase kinase 2 [Source:HGNC Symbol;Acc:HGNC:8810]"}, {"versioned_ensembl_gene_id":"ENSG00000137955.15","gene_symbol":"RABGGTB","gene_name":"Rab geranylgeranyltransferase beta subunit [Source:HGNC Symbol;Acc:HGNC:9796]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5876","summary":"This gene encodes the beta-subunit of the enzyme Rab geranylgeranyl-transferase (RabGGTase), which belongs to the protein prenyltransferase family. RabGGTase catalyzes the post-translational addition of geranylgeranyl groups to C-terminal cysteine residues of Rab GTPases. Three small nucleolar RNA genes are present in the intronic regions of this gene. Alternately spliced transcript variants have been observed for this gene. A pseudogene associated with this gene is located on chromosome 3. [provided by RefSeq, Jan 2013]","start":75786197,"end":75795079,"strand":1,"description":"Rab geranylgeranyltransferase beta subunit [Source:HGNC Symbol;Acc:HGNC:9796]"}, {"versioned_ensembl_gene_id":"ENSG00000246308.1","gene_symbol":"AC116535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10809297,"end":10822931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125954.12","gene_symbol":"CHURC1-FNTB","gene_name":"CHURC1-FNTB readthrough [Source:HGNC Symbol;Acc:HGNC:42960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529261","summary":"This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]","start":64914485,"end":65061803,"strand":1,"description":"CHURC1-FNTB readthrough [Source:HGNC Symbol;Acc:HGNC:42960]"}, {"versioned_ensembl_gene_id":"ENSG00000235679.1","gene_symbol":"AL161651.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30383400,"end":30383622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153944.10","gene_symbol":"MSI2","gene_name":"musashi RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:18585]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124540","summary":"This gene encodes an RNA-binding protein that is a member of the Musashi protein family. The encoded protein is transcriptional regulator that targets genes involved in development and cell cycle regulation. Mutations in this gene are associated with poor prognosis in certain types of cancers. This gene has also been shown to be rearranged in certain cancer cells. [provided by RefSeq, Apr 2016]","start":57255851,"end":57684685,"strand":1,"description":"musashi RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:18585]"}, {"versioned_ensembl_gene_id":"ENSG00000116016.13","gene_symbol":"EPAS1","gene_name":"endothelial PAS domain protein 1 [Source:HGNC Symbol;Acc:HGNC:3374]","synonyms":"PASD2,MOP2,HLF,HIF2A,bHLHe73","biotype":"protein_coding","ncbi_id":"2034","summary":"This gene encodes a transcription factor involved in the induction of genes regulated by oxygen, which is induced as oxygen levels fall. The encoded protein contains a basic-helix-loop-helix domain protein dimerization domain as well as a domain found in proteins in signal transduction pathways which respond to oxygen levels. Mutations in this gene are associated with erythrocytosis familial type 4. [provided by RefSeq, Nov 2009]","start":46293667,"end":46386703,"strand":1,"description":"endothelial PAS domain protein 1 [Source:HGNC Symbol;Acc:HGNC:3374]"}, {"versioned_ensembl_gene_id":"ENSG00000250027.1","gene_symbol":"AC022272.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":163108785,"end":163119965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235544.1","gene_symbol":"RPS11P1","gene_name":"ribosomal protein S11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16553]","synonyms":"dJ1060K6.1","biotype":"processed_pseudogene","ncbi_id":"128718","summary":null,"start":11345383,"end":11345855,"strand":-1,"description":"ribosomal protein S11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16553]"}, {"versioned_ensembl_gene_id":"ENSG00000136937.12","gene_symbol":"NCBP1","gene_name":"nuclear cap binding protein subunit 1 [Source:HGNC Symbol;Acc:HGNC:7658]","synonyms":"NCBP,CBP80,Sto1","biotype":"protein_coding","ncbi_id":"4686","summary":"The product of this gene is a component of the nuclear cap-binding protein complex (CBC), which binds to the monomethylated 5' cap of nascent pre-mRNA in the nucleoplasm. The encoded protein promotes high-affinity mRNA-cap binding and associates with the CTD of RNA polymerase II. The CBC promotes pre-mRNA splicing, 3'-end processing, RNA nuclear export, and nonsense-mediated mRNA decay. [provided by RefSeq, Jul 2008]","start":97633626,"end":97673748,"strand":1,"description":"nuclear cap binding protein subunit 1 [Source:HGNC Symbol;Acc:HGNC:7658]"}, {"versioned_ensembl_gene_id":"ENSG00000175766.11","gene_symbol":"EIF4E1B","gene_name":"eukaryotic translation initiation factor 4E family member 1B [Source:HGNC Symbol;Acc:HGNC:33179]","synonyms":"FLJ36951","biotype":"protein_coding","ncbi_id":"253314","summary":null,"start":176630682,"end":176646641,"strand":1,"description":"eukaryotic translation initiation factor 4E family member 1B [Source:HGNC Symbol;Acc:HGNC:33179]"}, {"versioned_ensembl_gene_id":"ENSG00000220831.4","gene_symbol":"NDUFA5P9","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48851]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289579","summary":null,"start":86214237,"end":86214576,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48851]"}, {"versioned_ensembl_gene_id":"ENSG00000246451.2","gene_symbol":"AL049840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103682362,"end":103684015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217272.1","gene_symbol":"AL049545.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86170447,"end":86171018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230245.2","gene_symbol":"BX088651.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42636788,"end":42637139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132906.17","gene_symbol":"CASP9","gene_name":"caspase 9 [Source:HGNC Symbol;Acc:HGNC:1511]","synonyms":"PPP1R56,MCH6,ICE-LAP6,APAF-3","biotype":"protein_coding","ncbi_id":"842","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein can undergo autoproteolytic processing and activation by the apoptosome, a protein complex of cytochrome c and the apoptotic peptidase activating factor 1; this step is thought to be one of the earliest in the caspase activation cascade. This protein is thought to play a central role in apoptosis and to be a tumor suppressor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":15490832,"end":15526534,"strand":-1,"description":"caspase 9 [Source:HGNC Symbol;Acc:HGNC:1511]"}, {"versioned_ensembl_gene_id":"ENSG00000126778.8","gene_symbol":"SIX1","gene_name":"SIX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10887]","synonyms":"DFNA23","biotype":"protein_coding","ncbi_id":"6495","summary":"The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3). [provided by RefSeq, Jul 2008]","start":60643415,"end":60658259,"strand":-1,"description":"SIX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10887]"}, {"versioned_ensembl_gene_id":"ENSG00000168404.12","gene_symbol":"MLKL","gene_name":"mixed lineage kinase domain like pseudokinase [Source:HGNC Symbol;Acc:HGNC:26617]","synonyms":"FLJ34389","biotype":"protein_coding","ncbi_id":"197259","summary":"This gene belongs to the protein kinase superfamily. The encoded protein contains a protein kinase-like domain; however, is thought to be inactive because it lacks several residues required for activity. This protein plays a critical role in tumor necrosis factor (TNF)-induced necroptosis, a programmed cell death process, via interaction with receptor-interacting protein 3 (RIP3), which is a key signaling molecule in necroptosis pathway. Inhibitor studies and knockdown of this gene inhibited TNF-induced necrosis. High levels of this protein and RIP3 are associated with inflammatory bowel disease in children. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2015]","start":74671855,"end":74700960,"strand":-1,"description":"mixed lineage kinase domain like pseudokinase [Source:HGNC Symbol;Acc:HGNC:26617]"}, {"versioned_ensembl_gene_id":"ENSG00000261522.5","gene_symbol":"AL845331.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":94575976,"end":94587183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253496.2","gene_symbol":"AC068992.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16676905,"end":16915044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158711.13","gene_symbol":"ELK4","gene_name":"ELK4, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3326]","synonyms":"SAP1","biotype":"protein_coding","ncbi_id":"2005","summary":"This gene is a member of the Ets family of transcription factors and of the ternary complex factor (TCF) subfamily. Proteins of the TCF subfamily form a ternary complex by binding to the the serum response factor and the serum reponse element in the promoter of the c-fos proto-oncogene. The protein encoded by this gene is phosphorylated by the kinases, MAPK1 and MAPK8. Several transcript variants have been described for this gene. [provided by RefSeq, Jul 2008]","start":205597556,"end":205631962,"strand":-1,"description":"ELK4, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:3326]"}, {"versioned_ensembl_gene_id":"ENSG00000253184.1","gene_symbol":"AC011586.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16604255,"end":16664879,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261134.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797321,"end":29799329,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000177427.12","gene_symbol":"MIEF2","gene_name":"mitochondrial elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:17920]","synonyms":"SMCR7,MiD49,MGC23130","biotype":"protein_coding","ncbi_id":"125170","summary":"This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]","start":18260534,"end":18266552,"strand":1,"description":"mitochondrial elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:17920]"}, {"versioned_ensembl_gene_id":"ENSG00000268894.6","gene_symbol":"PLCE1-AS1","gene_name":"PLCE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45193]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128054","summary":null,"start":94279277,"end":94287478,"strand":-1,"description":"PLCE1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45193]"}, {"versioned_ensembl_gene_id":"ENSG00000274997.1","gene_symbol":"HIST1H2AH","gene_name":"histone cluster 1 H2A family member h [Source:HGNC Symbol;Acc:HGNC:13671]","synonyms":"H2AFALii,H2A/S,dJ86C11.1","biotype":"protein_coding","ncbi_id":"85235","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]","start":27147129,"end":27147515,"strand":1,"description":"histone cluster 1 H2A family member h [Source:HGNC Symbol;Acc:HGNC:13671]"}, {"versioned_ensembl_gene_id":"ENSG00000228553.1","gene_symbol":"AL389885.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94225160,"end":94227288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258196.1","gene_symbol":"AL163973.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31553358,"end":31558498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218283.2","gene_symbol":"MORF4L1P1","gene_name":"mortality factor 4 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20400]","synonyms":"MRG1,MORF4LP1","biotype":"processed_pseudogene","ncbi_id":"326591","summary":null,"start":220253570,"end":220254536,"strand":1,"description":"mortality factor 4 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20400]"}, {"versioned_ensembl_gene_id":"ENSG00000215568.7","gene_symbol":"GAB4","gene_name":"GRB2 associated binding protein family member 4 [Source:HGNC Symbol;Acc:HGNC:18325]","synonyms":null,"biotype":"protein_coding","ncbi_id":"128954","summary":null,"start":16961936,"end":17008222,"strand":-1,"description":"GRB2 associated binding protein family member 4 [Source:HGNC Symbol;Acc:HGNC:18325]"}, {"versioned_ensembl_gene_id":"ENSG00000197903.7","gene_symbol":"HIST1H2BK","gene_name":"histone cluster 1 H2B family member k [Source:HGNC Symbol;Acc:HGNC:13954]","synonyms":"H2BFT,H2BFAiii","biotype":"protein_coding","ncbi_id":"85236","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-dependent histone that is a member of the histone H2B family. The protein encoded is an antimicrobial protein with antibacterial and antifungal activity. Two transcripts that encode the same protein have been identified for this gene, which is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]","start":27146418,"end":27146798,"strand":-1,"description":"histone cluster 1 H2B family member k [Source:HGNC Symbol;Acc:HGNC:13954]"}, {"versioned_ensembl_gene_id":"ENSG00000281658.1","gene_symbol":"AC138089.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":248486689,"end":248487928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181123.8","gene_symbol":"AC004832.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30475364,"end":30492804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181350.11","gene_symbol":"LRRC75A","gene_name":"leucine rich repeat containing 75A [Source:HGNC Symbol;Acc:HGNC:32403]","synonyms":"FAM211A,C17orf76,FLJ35696","biotype":"protein_coding","ncbi_id":"388341","summary":null,"start":16441577,"end":16492153,"strand":-1,"description":"leucine rich repeat containing 75A [Source:HGNC Symbol;Acc:HGNC:32403]"}, {"versioned_ensembl_gene_id":"ENSG00000225422.4","gene_symbol":"RBMS1P1","gene_name":"RNA binding motif single stranded interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9908]","synonyms":"RBMS1P,MSSP1","biotype":"processed_pseudogene","ncbi_id":"5938","summary":null,"start":66234079,"end":66235234,"strand":-1,"description":"RNA binding motif single stranded interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9908]"}, {"versioned_ensembl_gene_id":"ENSG00000230803.1","gene_symbol":"AC097532.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":132285795,"end":132294377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233786.1","gene_symbol":"CDC27P1","gene_name":"cell division cycle 27 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38091]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647696","summary":null,"start":132262328,"end":132263042,"strand":1,"description":"cell division cycle 27 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38091]"}, {"versioned_ensembl_gene_id":"ENSG00000230372.1","gene_symbol":"AL133268.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25061625,"end":25063507,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114124.2","gene_symbol":"GRK7","gene_name":"G protein-coupled receptor kinase 7 [Source:HGNC Symbol;Acc:HGNC:17031]","synonyms":"GPRK7","biotype":"protein_coding","ncbi_id":"131890","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. It is specifically expressed in the retina and the encoded protein has been shown to phosphorylate cone opsins and initiate their deactivation. [provided by RefSeq, Jul 2008]","start":141778148,"end":141818490,"strand":1,"description":"G protein-coupled receptor kinase 7 [Source:HGNC Symbol;Acc:HGNC:17031]"}, {"versioned_ensembl_gene_id":"ENSG00000251123.1","gene_symbol":"AC084752.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":162984795,"end":162985416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234841.4","gene_symbol":"AC017007.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112826307,"end":112827607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225571.1","gene_symbol":"AL845443.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31297920,"end":31298654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281613.2","gene_symbol":"AL365214.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112236806,"end":112350094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230930.8","gene_symbol":"COL11A2","gene_name":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]","synonyms":"DFNB53,DFNA13,HKE5","biotype":"protein_coding","ncbi_id":"1302","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]","start":33140587,"end":33170405,"strand":-1,"description":"collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]"}, {"versioned_ensembl_gene_id":"ENSG00000157551.17","gene_symbol":"KCNJ15","gene_name":"potassium voltage-gated channel subfamily J member 15 [Source:HGNC Symbol;Acc:HGNC:6261]","synonyms":"Kir4.2,Kir1.3,IRKK","biotype":"protein_coding","ncbi_id":"3772","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Eight transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2013]","start":38157034,"end":38307357,"strand":1,"description":"potassium voltage-gated channel subfamily J member 15 [Source:HGNC Symbol;Acc:HGNC:6261]"}, {"versioned_ensembl_gene_id":"ENSG00000141668.9","gene_symbol":"CBLN2","gene_name":"cerebellin 2 precursor [Source:HGNC Symbol;Acc:HGNC:1544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147381","summary":null,"start":72536680,"end":72638521,"strand":-1,"description":"cerebellin 2 precursor [Source:HGNC Symbol;Acc:HGNC:1544]"}, {"versioned_ensembl_gene_id":"ENSG00000250377.1","gene_symbol":"AC008525.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88692645,"end":88693972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227598.1","gene_symbol":"Z94721.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":166969626,"end":166999065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230002.2","gene_symbol":"ALMS1-IT1","gene_name":"ALMS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41305]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874291","summary":null,"start":73456764,"end":73459484,"strand":1,"description":"ALMS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41305]"}, {"versioned_ensembl_gene_id":"ENSG00000232388.4","gene_symbol":"SMIM26","gene_name":"small integral membrane protein 26 [Source:HGNC Symbol;Acc:HGNC:43430]","synonyms":"LINC00493,LOC388789","biotype":"protein_coding","ncbi_id":"388789","summary":null,"start":18567347,"end":18569563,"strand":1,"description":"small integral membrane protein 26 [Source:HGNC Symbol;Acc:HGNC:43430]"}, {"versioned_ensembl_gene_id":"ENSG00000281489.1","gene_symbol":"OR2T7","gene_name":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]","synonyms":"OST723,OR2T7P","biotype":"protein_coding","ncbi_id":"81458","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248443651,"end":248444577,"strand":1,"description":"olfactory receptor family 2 subfamily T member 7 [Source:HGNC Symbol;Acc:HGNC:15019]"}, {"versioned_ensembl_gene_id":"ENSG00000261030.1","gene_symbol":"AC079171.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13093660,"end":13094573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178229.7","gene_symbol":"ZNF543","gene_name":"zinc finger protein 543 [Source:HGNC Symbol;Acc:HGNC:25281]","synonyms":"DKFZp434H055","biotype":"protein_coding","ncbi_id":"125919","summary":null,"start":57320509,"end":57330776,"strand":1,"description":"zinc finger protein 543 [Source:HGNC Symbol;Acc:HGNC:25281]"}, {"versioned_ensembl_gene_id":"ENSG00000264281.3","gene_symbol":"AC016596.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55944656,"end":55944733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240366.1","gene_symbol":"AC113208.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75186651,"end":75186968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000063322.13","gene_symbol":"MED29","gene_name":"mediator complex subunit 29 [Source:HGNC Symbol;Acc:HGNC:23074]","synonyms":"MED2,IXL,DKFZp434H247","biotype":"protein_coding","ncbi_id":"55588","summary":"MED29 is a subunit of the Mediator complex, a multiprotein coactivator of RNA transcription that interacts with DNA-bound transcriptional activators, RNA polymerase II (see MIM 180660), and general initiation factors (Sato et al., 2003 [PubMed 14576168]).[supplied by OMIM, Aug 2009]","start":39391303,"end":39400637,"strand":1,"description":"mediator complex subunit 29 [Source:HGNC Symbol;Acc:HGNC:23074]"}, {"versioned_ensembl_gene_id":"ENSG00000270440.1","gene_symbol":"AC012175.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5838131,"end":5838661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282209.1","gene_symbol":"GOLGA6L17P","gene_name":"golgin A6 family-like 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:49414]","synonyms":"GOLGA6L21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"642402","summary":null,"start":82598917,"end":82605538,"strand":1,"description":"golgin A6 family-like 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:49414]"}, {"versioned_ensembl_gene_id":"ENSG00000242943.1","gene_symbol":"NKAIN1P1","gene_name":"sodium/potassium transporting ATPase interacting 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38593]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462647","summary":null,"start":143487772,"end":143488353,"strand":1,"description":"sodium/potassium transporting ATPase interacting 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38593]"}, {"versioned_ensembl_gene_id":"ENSG00000281249.1","gene_symbol":"AL049612.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":169809318,"end":169810102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181026.14","gene_symbol":"AEN","gene_name":"apoptosis enhancing nuclease [Source:HGNC Symbol;Acc:HGNC:25722]","synonyms":"ISG20L1,FLJ12562,FLJ12484","biotype":"protein_coding","ncbi_id":"64782","summary":null,"start":88621296,"end":88632282,"strand":1,"description":"apoptosis enhancing nuclease [Source:HGNC Symbol;Acc:HGNC:25722]"}, {"versioned_ensembl_gene_id":"ENSG00000250560.2","gene_symbol":"AC093870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75194867,"end":75195079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155097.11","gene_symbol":"ATP6V1C1","gene_name":"ATPase H+ transporting V1 subunit C1 [Source:HGNC Symbol;Acc:HGNC:856]","synonyms":"Vma5,VATC,ATP6D,ATP6C","biotype":"protein_coding","ncbi_id":"528","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene is one of two genes that encode the V1 domain C subunit proteins and is found ubiquitously. This C subunit is analogous but not homologous to gamma subunit of F-ATPases. Previously, this gene was designated ATP6D. [provided by RefSeq, Jul 2008]","start":103021063,"end":103073051,"strand":1,"description":"ATPase H+ transporting V1 subunit C1 [Source:HGNC Symbol;Acc:HGNC:856]"}, {"versioned_ensembl_gene_id":"ENSG00000089876.11","gene_symbol":"DHX32","gene_name":"DEAH-box helicase 32 (putative) [Source:HGNC Symbol;Acc:HGNC:16717]","synonyms":"FLJ10889,FLJ10694,DHLP1,DDX32","biotype":"protein_coding","ncbi_id":"55760","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. The function of this member has not been determined. Alternative splicing of this gene generates 2 transcript variants, but the full length nature of one of the variants has not been defined. [provided by RefSeq, Jul 2008]","start":125836337,"end":125896436,"strand":-1,"description":"DEAH-box helicase 32 (putative) [Source:HGNC Symbol;Acc:HGNC:16717]"}, {"versioned_ensembl_gene_id":"ENSG00000254481.1","gene_symbol":"AP000911.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134123828,"end":134124329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101474.11","gene_symbol":"APMAP","gene_name":"adipocyte plasma membrane associated protein [Source:HGNC Symbol;Acc:HGNC:13238]","synonyms":"C20orf3,BSCv","biotype":"protein_coding","ncbi_id":"57136","summary":null,"start":24962925,"end":24992979,"strand":-1,"description":"adipocyte plasma membrane associated protein [Source:HGNC Symbol;Acc:HGNC:13238]"}, {"versioned_ensembl_gene_id":"ENSG00000169618.6","gene_symbol":"PROKR1","gene_name":"prokineticin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4524]","synonyms":"ZAQ,PKR1,GPR73a,GPR73","biotype":"protein_coding","ncbi_id":"10887","summary":"This gene encodes a member of the G-protein-coupled receptor family. The encoded protein binds to prokineticins (1 and 2), leading to the activation of MAPK and STAT signaling pathways. Prokineticins are protein ligands involved in angiogenesis and inflammation. The encoded protein is expressed in peripheral tissues such as those comprising the circulatory system, lungs, reproductive system, endocrine system and the gastrointestinal system. The protein may be involved in signaling in human fetal ovary during initiation of primordial follicle formation. Sequence variants in this gene may be associated with recurrent miscarriage. [provided by RefSeq, Aug 2016]","start":68643589,"end":68658247,"strand":1,"description":"prokineticin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4524]"}, {"versioned_ensembl_gene_id":"ENSG00000230721.1","gene_symbol":"AL049597.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86784913,"end":86785467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272312.1","gene_symbol":"AL133255.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27001208,"end":27001648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242445.1","gene_symbol":"RPL7AP11","gene_name":"ribosomal protein L7a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35242]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728992","summary":null,"start":121494110,"end":121494908,"strand":1,"description":"ribosomal protein L7a pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35242]"}, {"versioned_ensembl_gene_id":"ENSG00000237234.7","gene_symbol":"Z99289.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112154765,"end":112166476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161896.11","gene_symbol":"IP6K3","gene_name":"inositol hexakisphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:17269]","synonyms":"INSP6K3,IHPK3","biotype":"protein_coding","ncbi_id":"117283","summary":"This gene encodes a protein that belongs to the inositol phosphokinase (IPK) family. This protein is likely responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Dec 2008]","start":33721670,"end":33746905,"strand":-1,"description":"inositol hexakisphosphate kinase 3 [Source:HGNC Symbol;Acc:HGNC:17269]"}, {"versioned_ensembl_gene_id":"ENSG00000275035.2","gene_symbol":"CCDC92","gene_name":"coiled-coil domain containing 92 [Source:HGNC Symbol;Acc:HGNC:29563]","synonyms":"FLJ22471","biotype":"protein_coding","ncbi_id":"80212","summary":null,"start":123918723,"end":123946006,"strand":-1,"description":"coiled-coil domain containing 92 [Source:HGNC Symbol;Acc:HGNC:29563]"}, {"versioned_ensembl_gene_id":"ENSG00000258660.1","gene_symbol":"AC006146.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":73698103,"end":73700351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262118.1","gene_symbol":"MTCO1P28","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52093]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075169","summary":null,"start":3367719,"end":3369246,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:52093]"}, {"versioned_ensembl_gene_id":"ENSG00000165304.7","gene_symbol":"MELK","gene_name":"maternal embryonic leucine zipper kinase [Source:HGNC Symbol;Acc:HGNC:16870]","synonyms":"KIAA0175","biotype":"protein_coding","ncbi_id":"9833","summary":null,"start":36572862,"end":36677683,"strand":1,"description":"maternal embryonic leucine zipper kinase [Source:HGNC Symbol;Acc:HGNC:16870]"}, {"versioned_ensembl_gene_id":"ENSG00000230319.1","gene_symbol":"AL022476.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43038585,"end":43052366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166562.8","gene_symbol":"SEC11C","gene_name":"SEC11 homolog C, signal peptidase complex subunit [Source:HGNC Symbol;Acc:HGNC:23400]","synonyms":"SPCS4C,SPC21,SEC11L3","biotype":"protein_coding","ncbi_id":"90701","summary":null,"start":59139477,"end":59158836,"strand":1,"description":"SEC11 homolog C, signal peptidase complex subunit [Source:HGNC Symbol;Acc:HGNC:23400]"}, {"versioned_ensembl_gene_id":"ENSG00000279306.1","gene_symbol":"AL139288.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":228486188,"end":228487120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168159.11","gene_symbol":"RNF187","gene_name":"ring finger protein 187 [Source:HGNC Symbol;Acc:HGNC:27146]","synonyms":"RACO1,RACO-1","biotype":"protein_coding","ncbi_id":"149603","summary":null,"start":228487061,"end":228495766,"strand":1,"description":"ring finger protein 187 [Source:HGNC Symbol;Acc:HGNC:27146]"}, {"versioned_ensembl_gene_id":"ENSG00000275974.2","gene_symbol":"PPIAL4F","gene_name":"peptidylprolyl isomerase A like 4F [Source:HGNC Symbol;Acc:HGNC:33999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728945","summary":null,"start":144592865,"end":144593524,"strand":1,"description":"peptidylprolyl isomerase A like 4F [Source:HGNC Symbol;Acc:HGNC:33999]"}, {"versioned_ensembl_gene_id":"ENSG00000270178.1","gene_symbol":"AC007687.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179804063,"end":179804366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228559.1","gene_symbol":"AL033519.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35544632,"end":35545669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203489.3","gene_symbol":"HMGB1P39","gene_name":"high mobility group box 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39186]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419972","summary":null,"start":75319101,"end":75319980,"strand":-1,"description":"high mobility group box 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:39186]"}, {"versioned_ensembl_gene_id":"ENSG00000239944.1","gene_symbol":"TRBV8-2","gene_name":"T-cell receptor beta variable 8-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12245]","synonyms":"TRBV82,TCRBV32S1P","biotype":"TR_V_pseudogene","ncbi_id":"28587","summary":null,"start":142386378,"end":142386647,"strand":1,"description":"T-cell receptor beta variable 8-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12245]"}, {"versioned_ensembl_gene_id":"ENSG00000263177.1","gene_symbol":"MTND1P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287461","summary":null,"start":3369957,"end":3370906,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42100]"}, {"versioned_ensembl_gene_id":"ENSG00000078328.20","gene_symbol":"RBFOX1","gene_name":"RNA binding protein, fox-1 homolog 1 [Source:HGNC Symbol;Acc:HGNC:18222]","synonyms":"HRNBP1,FOX-1,A2BP1","biotype":"protein_coding","ncbi_id":"54715","summary":"The Fox-1 family of RNA-binding proteins is evolutionarily conserved, and regulates tissue-specific alternative splicing in metazoa. Fox-1 recognizes a (U)GCAUG stretch in regulated exons or in flanking introns. The protein binds to the C-terminus of ataxin-2 and may contribute to the restricted pathology of spinocerebellar ataxia type 2 (SCA2). Ataxin-2 is the product of the SCA2 gene which causes familial neurodegenerative diseases. Fox-1 and ataxin-2 are both localized in the trans-Golgi network. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":5239802,"end":7713338,"strand":1,"description":"RNA binding protein, fox-1 homolog 1 [Source:HGNC Symbol;Acc:HGNC:18222]"}, {"versioned_ensembl_gene_id":"ENSG00000257180.1","gene_symbol":"AC009135.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6056975,"end":6092954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267101.5","gene_symbol":"AC090376.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45130565,"end":45181347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198951.11","gene_symbol":"NAGA","gene_name":"alpha-N-acetylgalactosaminidase [Source:HGNC Symbol;Acc:HGNC:7631]","synonyms":"D22S674","biotype":"protein_coding","ncbi_id":"4668","summary":"NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease). [provided by RefSeq, Jul 2008]","start":42058354,"end":42070842,"strand":-1,"description":"alpha-N-acetylgalactosaminidase [Source:HGNC Symbol;Acc:HGNC:7631]"}, {"versioned_ensembl_gene_id":"ENSG00000268036.1","gene_symbol":"AC007228.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":56613810,"end":56613951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231336.1","gene_symbol":"AC017006.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46166789,"end":46167978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228481.1","gene_symbol":"U51244.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45674701,"end":45675476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234168.2","gene_symbol":"LINC01039","gene_name":"long intergenic non-protein coding RNA 1039 [Source:HGNC Symbol;Acc:HGNC:49027]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355149","summary":null,"start":99577112,"end":99580368,"strand":1,"description":"long intergenic non-protein coding RNA 1039 [Source:HGNC Symbol;Acc:HGNC:49027]"}, {"versioned_ensembl_gene_id":"ENSG00000275846.1","gene_symbol":"AL513548.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26602733,"end":26606661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230133.1","gene_symbol":"LINC01721","gene_name":"long intergenic non-protein coding RNA 1721 [Source:HGNC Symbol;Acc:HGNC:52508]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400839","summary":null,"start":24199767,"end":24224588,"strand":1,"description":"long intergenic non-protein coding RNA 1721 [Source:HGNC Symbol;Acc:HGNC:52508]"}, {"versioned_ensembl_gene_id":"ENSG00000224638.1","gene_symbol":"AC106900.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173880865,"end":173899428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277009.1","gene_symbol":"AC244097.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":154233615,"end":154251288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236151.1","gene_symbol":"AL110503.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24142590,"end":24144386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211710.3","gene_symbol":"TRBV4-1","gene_name":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]","synonyms":"BV07S1J2.7,TRBV41,TCRBV7S1A1N2T,TCRBV4S1","biotype":"TR_V_gene","ncbi_id":"28617","summary":null,"start":142313184,"end":142313666,"strand":1,"description":"T-cell receptor beta variable 4-1 [Source:HGNC Symbol;Acc:HGNC:12215]"}, {"versioned_ensembl_gene_id":"ENSG00000167195.7","gene_symbol":"GOLGA6C","gene_name":"golgin A6 family member C [Source:HGNC Symbol;Acc:HGNC:32206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653641","summary":null,"start":75258599,"end":75270199,"strand":1,"description":"golgin A6 family member C [Source:HGNC Symbol;Acc:HGNC:32206]"}, {"versioned_ensembl_gene_id":"ENSG00000271179.1","gene_symbol":"AC098826.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":132080290,"end":132080755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236485.1","gene_symbol":"LINC01945","gene_name":"long intergenic non-protein coding RNA 1945 [Source:HGNC Symbol;Acc:HGNC:52769]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928067","summary":null,"start":131983937,"end":131994161,"strand":-1,"description":"long intergenic non-protein coding RNA 1945 [Source:HGNC Symbol;Acc:HGNC:52769]"}, {"versioned_ensembl_gene_id":"ENSG00000188460.4","gene_symbol":"ACTBP11","gene_name":"actin, beta pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:33971]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644220","summary":null,"start":223863726,"end":223864851,"strand":-1,"description":"actin, beta pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:33971]"}, {"versioned_ensembl_gene_id":"ENSG00000226553.1","gene_symbol":"AC018735.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187001876,"end":187003377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189149.12","gene_symbol":"CRYM-AS1","gene_name":"CRYM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34405]","synonyms":"NCRNA00169,FLJ41766","biotype":"transcribed_unitary_pseudogene","ncbi_id":"400508","summary":null,"start":21300849,"end":21339037,"strand":1,"description":"CRYM antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34405]"}, {"versioned_ensembl_gene_id":"ENSG00000108684.14","gene_symbol":"ASIC2","gene_name":"acid sensing ion channel subunit 2 [Source:HGNC Symbol;Acc:HGNC:99]","synonyms":"MDEG,hBNaC1,BNC1,BNaC1,ASIC2a,ACCN1,ACCN","biotype":"protein_coding","ncbi_id":"40","summary":"This gene encodes a member of the degenerin/epithelial sodium channel (DEG/ENaC) superfamily. The members of this family are amiloride-sensitive sodium channels that contain intracellular N and C termini, 2 hydrophobic transmembrane regions, and a large extracellular loop, which has many cysteine residues with conserved spacing. The member encoded by this gene may play a role in neurotransmission. In addition, a heteromeric association between this member and acid-sensing (proton-gated) ion channel 3 has been observed to co-assemble into proton-gated channels sensitive to gadolinium. Alternative splicing has been observed at this locus and two variants, encoding distinct isoforms, have been identified. [provided by RefSeq, Feb 2012]","start":33013087,"end":34174964,"strand":-1,"description":"acid sensing ion channel subunit 2 [Source:HGNC Symbol;Acc:HGNC:99]"}, {"versioned_ensembl_gene_id":"ENSG00000282504.1","gene_symbol":"IGHV7-56","gene_name":"immunoglobulin heavy variable 7-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5667]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28380","summary":null,"start":106634443,"end":106634877,"strand":-1,"description":"immunoglobulin heavy variable 7-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5667]"}, {"versioned_ensembl_gene_id":"ENSG00000105656.12","gene_symbol":"ELL","gene_name":"elongation factor for RNA polymerase II [Source:HGNC Symbol;Acc:HGNC:23114]","synonyms":"Men,ELL1,C19orf17,PPP1R68","biotype":"protein_coding","ncbi_id":"8178","summary":null,"start":18442663,"end":18522127,"strand":-1,"description":"elongation factor for RNA polymerase II [Source:HGNC Symbol;Acc:HGNC:23114]"}, {"versioned_ensembl_gene_id":"ENSG00000276880.3","gene_symbol":"IFI27L1","gene_name":"interferon alpha inducible protein 27 like 1 [Source:HGNC Symbol;Acc:HGNC:19754]","synonyms":"FAM14B","biotype":"protein_coding","ncbi_id":"122509","summary":null,"start":94081282,"end":94103846,"strand":1,"description":"interferon alpha inducible protein 27 like 1 [Source:HGNC Symbol;Acc:HGNC:19754]"}, {"versioned_ensembl_gene_id":"ENSG00000283398.1","gene_symbol":"AC114737.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":76960571,"end":76978658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269897.5","gene_symbol":"COMMD3-BMI1","gene_name":"COMMD3-BMI1 readthrough [Source:HGNC Symbol;Acc:HGNC:48326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532731","summary":"This locus represents naturally occurring read-through transcription between the neighboring COMM domain-containing protein 3 and polycomb complex protein BMI-1 genes on chromosome 10. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]","start":22316388,"end":22329542,"strand":1,"description":"COMMD3-BMI1 readthrough [Source:HGNC Symbol;Acc:HGNC:48326]"}, {"versioned_ensembl_gene_id":"ENSG00000279294.1","gene_symbol":"AC092135.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81618505,"end":81620563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203724.10","gene_symbol":"C1orf53","gene_name":"chromosome 1 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:30003]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388722","summary":null,"start":197902647,"end":197907367,"strand":1,"description":"chromosome 1 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:30003]"}, {"versioned_ensembl_gene_id":"ENSG00000238156.1","gene_symbol":"AL445465.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75454944,"end":75458900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260571.1","gene_symbol":"BNIP3P5","gene_name":"BCL2 interacting protein 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39658]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421724","summary":null,"start":42313687,"end":42314386,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39658]"}, {"versioned_ensembl_gene_id":"ENSG00000183696.13","gene_symbol":"UPP1","gene_name":"uridine phosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:12576]","synonyms":"UPP,UPASE,UP,UDRPASE","biotype":"protein_coding","ncbi_id":"7378","summary":"This gene encodes a uridine phosphorylase, an enzyme that catalyzes the reversible phosphorylation of uridine (or 2'- deoxyuridine) to uracil and ribose-1-phosphate (or deoxyribose-1-phosphate). The encoded enzyme functions in the degradation and salvage of pyrimidine ribonucleosides. [provided by RefSeq, Oct 2016]","start":48088628,"end":48108733,"strand":1,"description":"uridine phosphorylase 1 [Source:HGNC Symbol;Acc:HGNC:12576]"}, {"versioned_ensembl_gene_id":"ENSG00000133321.10","gene_symbol":"RARRES3","gene_name":"retinoic acid receptor responder 3 [Source:HGNC Symbol;Acc:HGNC:9869]","synonyms":"TIG3,HRASLS4","biotype":"protein_coding","ncbi_id":"5920","summary":"Retinoids exert biologic effects such as potent growth inhibitory and cell differentiation activities and are used in the treatment of hyperproliferative dermatological diseases. These effects are mediated by specific nuclear receptor proteins that are members of the steroid and thyroid hormone receptor superfamily of transcriptional regulators. RARRES1, RARRES2, and RARRES3 are genes whose expression is upregulated by the synthetic retinoid tazarotene. RARRES3 is thought act as a tumor suppressor or growth regulator. [provided by RefSeq, Jul 2008]","start":63536809,"end":63546462,"strand":1,"description":"retinoic acid receptor responder 3 [Source:HGNC Symbol;Acc:HGNC:9869]"}, {"versioned_ensembl_gene_id":"ENSG00000163013.11","gene_symbol":"FBXO41","gene_name":"F-box protein 41 [Source:HGNC Symbol;Acc:HGNC:29409]","synonyms":"KIAA1940,Fbx41","biotype":"protein_coding","ncbi_id":"150726","summary":"This gene encodes a member of the F-box protein family, which is characterized by an approximately 40 amino acid motif, the F-box. F-box proteins constitute one of the four subunits of the SCF ubiquitin protein ligase complex that plays a role in phosphorylation-dependent ubiquitination. F-box proteins are divided into three classes depending on the interaction substrate domain each contains in addition to the F-box motif: FBXW proteins contain WD-40 domains, FBXL proteins contain leucine-rich repeats, and FBXO proteins contain either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the FBXO class. [provided by RefSeq, Feb 2014]","start":73254682,"end":73284431,"strand":-1,"description":"F-box protein 41 [Source:HGNC Symbol;Acc:HGNC:29409]"}, {"versioned_ensembl_gene_id":"ENSG00000250994.1","gene_symbol":"AC005355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134436711,"end":134492519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187664.8","gene_symbol":"HAPLN4","gene_name":"hyaluronan and proteoglycan link protein 4 [Source:HGNC Symbol;Acc:HGNC:31357]","synonyms":"BRAL2,KIAA1926","biotype":"protein_coding","ncbi_id":"404037","summary":null,"start":19255641,"end":19262796,"strand":-1,"description":"hyaluronan and proteoglycan link protein 4 [Source:HGNC Symbol;Acc:HGNC:31357]"}, {"versioned_ensembl_gene_id":"ENSG00000008083.13","gene_symbol":"JARID2","gene_name":"jumonji and AT-rich interaction domain containing 2 [Source:HGNC Symbol;Acc:HGNC:6196]","synonyms":"JMJ","biotype":"protein_coding","ncbi_id":"3720","summary":"This gene encodes a Jumonji- and AT-rich interaction domain (ARID)-domain-containing protein. The encoded protein is a DNA-binding protein that functions as a transcriptional repressor. This protein interacts with the Polycomb repressive complex 2 (PRC2) which plays an essential role in regulating gene expression during embryonic development. This protein facilitates the recruitment of the PRC2 complex to target genes. Alternate splicing results in multiple transcript variants. Mutations in this gene are associated with chronic myeloid malignancies. [provided by RefSeq, May 2012]","start":15246296,"end":15522040,"strand":1,"description":"jumonji and AT-rich interaction domain containing 2 [Source:HGNC Symbol;Acc:HGNC:6196]"}, {"versioned_ensembl_gene_id":"ENSG00000178896.8","gene_symbol":"EXOSC4","gene_name":"exosome component 4 [Source:HGNC Symbol;Acc:HGNC:18189]","synonyms":"Ski6p,SKI6,Rrp41p,RRP41A,RRP41,p12A,hRrp41p,FLJ20591","biotype":"protein_coding","ncbi_id":"54512","summary":null,"start":144078626,"end":144080647,"strand":1,"description":"exosome component 4 [Source:HGNC Symbol;Acc:HGNC:18189]"}, {"versioned_ensembl_gene_id":"ENSG00000149972.10","gene_symbol":"CNTN5","gene_name":"contactin 5 [Source:HGNC Symbol;Acc:HGNC:2175]","synonyms":"NB-2,hNB-2","biotype":"protein_coding","ncbi_id":"53942","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily, and contactin family, which mediate cell surface interactions during nervous system development. This protein is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":99020953,"end":100358885,"strand":1,"description":"contactin 5 [Source:HGNC Symbol;Acc:HGNC:2175]"}, {"versioned_ensembl_gene_id":"ENSG00000196240.4","gene_symbol":"OR2T2","gene_name":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]","synonyms":"OR2T2P","biotype":"protein_coding","ncbi_id":"401992","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248445512,"end":248455725,"strand":1,"description":"olfactory receptor family 2 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:14725]"}, {"versioned_ensembl_gene_id":"ENSG00000277442.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54906159,"end":54910074,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000228889.6","gene_symbol":"UBAC2-AS1","gene_name":"UBAC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42502]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289373","summary":null,"start":99196377,"end":99200710,"strand":-1,"description":"UBAC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42502]"}, {"versioned_ensembl_gene_id":"ENSG00000271495.1","gene_symbol":"AC020765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28548331,"end":28548658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197487.8","gene_symbol":"GALP","gene_name":"galanin like peptide [Source:HGNC Symbol;Acc:HGNC:24840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85569","summary":"This gene encodes a member of the galanin family of neuropeptides. The encoded protein binds galanin receptors 1, 2 and 3 with the highest affinity for galanin receptor 3 and has been implicated in biological processes involving the central nervous system including hypothalamic regulation of metabolism and reproduction. A peptide encoded by a splice variant of this gene, termed alarin, has vasoactive properties, displays antimicrobial activity against E. coli, and may serve as a marker for neuroblastic tumors.[provided by RefSeq, Nov 2014]","start":56176020,"end":56185775,"strand":1,"description":"galanin like peptide [Source:HGNC Symbol;Acc:HGNC:24840]"}, {"versioned_ensembl_gene_id":"ENSG00000250863.1","gene_symbol":"AC110799.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43980006,"end":43981620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224644.1","gene_symbol":"AL135787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111574192,"end":111575427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124399.4","gene_symbol":"NDUFB4P12","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:45260]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402175","summary":null,"start":43898962,"end":43899351,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:45260]"}, {"versioned_ensembl_gene_id":"ENSG00000234005.3","gene_symbol":"GAPDHP22","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37774]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390421","summary":null,"start":99190579,"end":99190991,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:37774]"}, {"versioned_ensembl_gene_id":"ENSG00000099625.12","gene_symbol":"CBARP","gene_name":"CACN beta subunit associated regulatory protein [Source:HGNC Symbol;Acc:HGNC:28617]","synonyms":"MGC40084,DOS,C19orf26,BARP","biotype":"protein_coding","ncbi_id":"255057","summary":null,"start":1228287,"end":1238027,"strand":-1,"description":"CACN beta subunit associated regulatory protein [Source:HGNC Symbol;Acc:HGNC:28617]"}, {"versioned_ensembl_gene_id":"ENSG00000254833.1","gene_symbol":"AP001893.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126160714,"end":126176035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261257.1","gene_symbol":"AP000821.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126100505,"end":126102413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138801.8","gene_symbol":"PAPSS1","gene_name":"3'-phosphoadenosine 5'-phosphosulfate synthase 1 [Source:HGNC Symbol;Acc:HGNC:8603]","synonyms":"PAPSS,ATPSK1","biotype":"protein_coding","ncbi_id":"9061","summary":"Three-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS) is the sulfate donor cosubstrate for all sulfotransferase (SULT) enzymes (Xu et al., 2000 [PubMed 10679223]). SULTs catalyze the sulfate conjugation of many endogenous and exogenous compounds, including drugs and other xenobiotics. In humans, PAPS is synthesized from adenosine 5-prime triphosphate (ATP) and inorganic sulfate by 2 isoforms, PAPSS1 and PAPSS2 (MIM 603005).[supplied by OMIM, Mar 2008]","start":107590276,"end":107720452,"strand":-1,"description":"3'-phosphoadenosine 5'-phosphosulfate synthase 1 [Source:HGNC Symbol;Acc:HGNC:8603]"}, {"versioned_ensembl_gene_id":"ENSG00000168268.10","gene_symbol":"NT5DC2","gene_name":"5'-nucleotidase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25717]","synonyms":"FLJ12442","biotype":"protein_coding","ncbi_id":"64943","summary":null,"start":52524385,"end":52535054,"strand":-1,"description":"5'-nucleotidase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25717]"}, {"versioned_ensembl_gene_id":"ENSG00000234540.1","gene_symbol":"AL080313.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14394326,"end":14404289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130287.13","gene_symbol":"NCAN","gene_name":"neurocan [Source:HGNC Symbol;Acc:HGNC:2465]","synonyms":"CSPG3","biotype":"protein_coding","ncbi_id":"1463","summary":"Neurocan is a chondroitin sulfate proteoglycan thought to be involved in the modulation of cell adhesion and migration.[supplied by OMIM, Jul 2002]","start":19211973,"end":19252233,"strand":1,"description":"neurocan [Source:HGNC Symbol;Acc:HGNC:2465]"}, {"versioned_ensembl_gene_id":"ENSG00000230631.1","gene_symbol":"AL353152.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14229775,"end":14231570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267736.2","gene_symbol":"HMGB2P1","gene_name":"high mobility group box 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39174]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729119","summary":null,"start":1203209,"end":1203842,"strand":1,"description":"high mobility group box 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39174]"}, {"versioned_ensembl_gene_id":"ENSG00000227241.1","gene_symbol":"AC011998.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178105637,"end":178105753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179131.7","gene_symbol":"AC073335.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66914581,"end":66914943,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198203.9","gene_symbol":"SULT1C2","gene_name":"sulfotransferase family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:11456]","synonyms":"SULT1C1,ST1C1","biotype":"protein_coding","ncbi_id":"6819","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that belongs to the SULT1 subfamily, responsible for transferring a sulfo moiety from PAPS to phenol-containing compounds. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":108288639,"end":108309915,"strand":1,"description":"sulfotransferase family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:11456]"}, {"versioned_ensembl_gene_id":"ENSG00000255380.1","gene_symbol":"AP001317.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98130239,"end":98131198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260177.1","gene_symbol":"AC126696.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87780134,"end":87806476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242705.1","gene_symbol":"ICE2P2","gene_name":"interactor of little elongation complex ELL subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48857]","synonyms":"NARG2P2","biotype":"processed_pseudogene","ncbi_id":"728432","summary":null,"start":88948142,"end":88950928,"strand":1,"description":"interactor of little elongation complex ELL subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48857]"}, {"versioned_ensembl_gene_id":"ENSG00000281624.1","gene_symbol":"AC131097.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241808312,"end":241812016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233801.9","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"NELF-E,RDBP,D6S45,RD,RDP","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31944741,"end":31951746,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000155011.8","gene_symbol":"DKK2","gene_name":"dickkopf WNT signaling pathway inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:2892]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27123","summary":"This gene encodes a protein that is a member of the dickkopf family. The secreted protein contains two cysteine rich regions and is involved in embryonic development through its interactions with the Wnt signaling pathway. It can act as either an agonist or antagonist of Wnt/beta-catenin signaling, depending on the cellular context and the presence of the co-factor kremen 2. Activity of this protein is also modulated by binding to the Wnt co-receptor LDL-receptor related protein 6 (LRP6). [provided by RefSeq, Jul 2008]","start":106921802,"end":107283806,"strand":-1,"description":"dickkopf WNT signaling pathway inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:2892]"}, {"versioned_ensembl_gene_id":"ENSG00000244998.1","gene_symbol":"AC100803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141389939,"end":141392574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269559.2","gene_symbol":"AC093677.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74156511,"end":74158373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157514.16","gene_symbol":"TSC22D3","gene_name":"TSC22 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:3051]","synonyms":"TSC-22R,hDIP,GILZ,DSIPI,DIP","biotype":"protein_coding","ncbi_id":"1831","summary":"This gene encodes the anti-inflammatory protein glucocorticoid (GC)-induced leucine zipper. Expression of this gene stimulated by glucocorticoids and interleukin 10 and it appears to play a key role in the anti-inflammatory and immunosuppressive effects of this steroid. This protein has also been shown to inhibit pro-inflammatory molecules including nuclear factor κB. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":107713221,"end":107777342,"strand":-1,"description":"TSC22 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:3051]"}, {"versioned_ensembl_gene_id":"ENSG00000174306.21","gene_symbol":"ZHX3","gene_name":"zinc fingers and homeoboxes 3 [Source:HGNC Symbol;Acc:HGNC:15935]","synonyms":"TIX1,KIAA0395","biotype":"protein_coding","ncbi_id":"23051","summary":"This gene encodes a member of the zinc fingers and homeoboxes (ZHX) gene family. The encoded protein contains two C2H2-type zinc fingers and five homeodomains and forms a dimer with itself or with zinc fingers and homeoboxes family member 1. In the nucleus, the dimerized protein interacts with the A subunit of the ubiquitous transcription factor nuclear factor-Y and may function as a transcriptional repressor. [provided by RefSeq, Jul 2008]","start":41178448,"end":41317672,"strand":-1,"description":"zinc fingers and homeoboxes 3 [Source:HGNC Symbol;Acc:HGNC:15935]"}, {"versioned_ensembl_gene_id":"ENSG00000233040.2","gene_symbol":"FAM204BP","gene_name":"family with sequence similarity 204 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:42011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420875","summary":null,"start":197746751,"end":197747451,"strand":-1,"description":"family with sequence similarity 204 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:42011]"}, {"versioned_ensembl_gene_id":"ENSG00000228374.1","gene_symbol":"AC012497.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139732708,"end":139733282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226946.1","gene_symbol":"AC062022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161568502,"end":161570185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166473.17","gene_symbol":"PKD1L2","gene_name":"polycystin 1 like 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:21715]","synonyms":"KIAA1879","biotype":"polymorphic_pseudogene","ncbi_id":"114780","summary":"This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores. This gene appears to be a polymorphic pseudogene in humans, and the reference genome encodes a non-functional allele. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2019]","start":81100875,"end":81220370,"strand":-1,"description":"polycystin 1 like 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:21715]"}, {"versioned_ensembl_gene_id":"ENSG00000257493.1","gene_symbol":"AL512310.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19664098,"end":19683677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260487.1","gene_symbol":"AC116348.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30480588,"end":30481346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155275.18","gene_symbol":"TRMT44","gene_name":"tRNA methyltransferase 44 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:26653]","synonyms":"C4orf23,TRM44,METTL19,FLJ35725","biotype":"protein_coding","ncbi_id":"152992","summary":"The protein encoded by this gene is a putative tRNA methyltransferase found in the cytoplasm. Defects in this gene may be a cause of partial epilepsy with pericentral spikes (PEPS), but that has not been proven definitively. [provided by RefSeq, May 2012]","start":8436140,"end":8493531,"strand":1,"description":"tRNA methyltransferase 44 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:26653]"}, {"versioned_ensembl_gene_id":"ENSG00000251186.1","gene_symbol":"AC105345.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8453410,"end":8454942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277781.2","gene_symbol":"MROH6","gene_name":"maestro heat like repeat family member 6 [Source:HGNC Symbol;Acc:HGNC:27814]","synonyms":"C8orf73","biotype":"protein_coding","ncbi_id":"642475","summary":null,"start":143566187,"end":143572971,"strand":-1,"description":"maestro heat like repeat family member 6 [Source:HGNC Symbol;Acc:HGNC:27814]"}, {"versioned_ensembl_gene_id":"ENSG00000204663.9","gene_symbol":"CST13P","gene_name":"cystatin 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:44335]","synonyms":"CTES6,CSTT","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"164380","summary":null,"start":23519146,"end":23542018,"strand":1,"description":"cystatin 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:44335]"}, {"versioned_ensembl_gene_id":"ENSG00000275232.1","gene_symbol":"AC073578.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131447337,"end":131455436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204103.3","gene_symbol":"MAFB","gene_name":"MAF bZIP transcription factor B [Source:HGNC Symbol;Acc:HGNC:6408]","synonyms":"KRML","biotype":"protein_coding","ncbi_id":"9935","summary":"The protein encoded by this gene is a basic leucine zipper (bZIP) transcription factor that plays an important role in the regulation of lineage-specific hematopoiesis. The encoded nuclear protein represses ETS1-mediated transcription of erythroid-specific genes in myeloid cells. This gene contains no introns. [provided by RefSeq, Jul 2008]","start":40685848,"end":40689240,"strand":-1,"description":"MAF bZIP transcription factor B [Source:HGNC Symbol;Acc:HGNC:6408]"}, {"versioned_ensembl_gene_id":"ENSG00000181092.9","gene_symbol":"ADIPOQ","gene_name":"adiponectin, C1Q and collagen domain containing [Source:HGNC Symbol;Acc:HGNC:13633]","synonyms":"ACRP30,ACDC,GBP28,apM1,AdipoQ,adiponectin","biotype":"protein_coding","ncbi_id":"9370","summary":"This gene is expressed in adipose tissue exclusively. It encodes a protein with similarity to collagens X and VIII and complement factor C1q. The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes. Mutations in this gene are associated with adiponectin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Apr 2010]","start":186842690,"end":186858463,"strand":1,"description":"adiponectin, C1Q and collagen domain containing [Source:HGNC Symbol;Acc:HGNC:13633]"}, {"versioned_ensembl_gene_id":"ENSG00000115268.9","gene_symbol":"RPS15","gene_name":"ribosomal protein S15 [Source:HGNC Symbol;Acc:HGNC:10388]","synonyms":"S15,RIG,MGC111130","biotype":"protein_coding","ncbi_id":"6209","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S19P family of ribosomal proteins. It is located in the cytoplasm. This gene has been found to be activated in various tumors, such as insulinomas, esophageal cancers, and colon cancers. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":1438358,"end":1440494,"strand":1,"description":"ribosomal protein S15 [Source:HGNC Symbol;Acc:HGNC:10388]"}, {"versioned_ensembl_gene_id":"ENSG00000085415.15","gene_symbol":"SEH1L","gene_name":"SEH1 like nucleoporin [Source:HGNC Symbol;Acc:HGNC:30379]","synonyms":"SEH1B,SEH1A,Seh1,SEC13L","biotype":"protein_coding","ncbi_id":"81929","summary":"The protein encoded by this gene is part of a nuclear pore complex, Nup107-160. This protein contains WD repeats and shares 34% amino acid identity with yeast Seh1 and 30% identity with yeast Sec13. All constituents of the Nup107-160 complex, including this protein, specifically localize to kinetochores in mitosis. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":12947133,"end":12987536,"strand":1,"description":"SEH1 like nucleoporin [Source:HGNC Symbol;Acc:HGNC:30379]"}, {"versioned_ensembl_gene_id":"ENSG00000006606.8","gene_symbol":"CCL26","gene_name":"C-C motif chemokine ligand 26 [Source:HGNC Symbol;Acc:HGNC:10625]","synonyms":"TSC-1,SCYA26,MIP-4alpha,MIP-4a,IMAC,eotaxin-3","biotype":"protein_coding","ncbi_id":"10344","summary":"This gene is one of two Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 7. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for normal peripheral blood eosinophils and basophils. This protein also has antimicrobial activity, displaying an antibacterial effect on S. pneumoniae, S. aureus, Non-typeable H. influenzae, and P. aeruginosa. The product of this gene is one of three related chemokines that specifically activate chemokine receptor CCR3. This chemokine may contribute to the eosinophil accumulation in atopic diseases. [provided by RefSeq, Jul 2020]","start":75769533,"end":75789896,"strand":-1,"description":"C-C motif chemokine ligand 26 [Source:HGNC Symbol;Acc:HGNC:10625]"}, {"versioned_ensembl_gene_id":"ENSG00000016864.18","gene_symbol":"GLT8D1","gene_name":"glycosyltransferase 8 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24870]","synonyms":"FLJ14611,AD-017","biotype":"protein_coding","ncbi_id":"55830","summary":"This gene encodes a member of the glycosyltransferase family. The specific function of this protein has not been determined. Alternative splicing results in multiple transcript variants of this gene [provided by RefSeq, May 2013]","start":52694488,"end":52706032,"strand":-1,"description":"glycosyltransferase 8 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24870]"}, {"versioned_ensembl_gene_id":"ENSG00000162576.16","gene_symbol":"MXRA8","gene_name":"matrix remodeling associated 8 [Source:HGNC Symbol;Acc:HGNC:7542]","synonyms":"DKFZp586E2023","biotype":"protein_coding","ncbi_id":"54587","summary":null,"start":1352689,"end":1361777,"strand":-1,"description":"matrix remodeling associated 8 [Source:HGNC Symbol;Acc:HGNC:7542]"}, {"versioned_ensembl_gene_id":"ENSG00000113643.8","gene_symbol":"RARS","gene_name":"arginyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:9870]","synonyms":"DALRD1","biotype":"protein_coding","ncbi_id":"5917","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Arginyl-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family. [provided by RefSeq, Jul 2008]","start":168486445,"end":168519299,"strand":1,"description":"arginyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:9870]"}, {"versioned_ensembl_gene_id":"ENSG00000248319.1","gene_symbol":"LINC02275","gene_name":"long intergenic non-protein coding RNA 2275 [Source:HGNC Symbol;Acc:HGNC:53191]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506085","summary":null,"start":169917761,"end":169975902,"strand":-1,"description":"long intergenic non-protein coding RNA 2275 [Source:HGNC Symbol;Acc:HGNC:53191]"}, {"versioned_ensembl_gene_id":"ENSG00000254070.1","gene_symbol":"AC104576.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46671839,"end":46671926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251200.1","gene_symbol":"AC084866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169945981,"end":169963334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251470.1","gene_symbol":"ASNSP4","gene_name":"asparagine synthetase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39400]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419423","summary":null,"start":46697630,"end":46698688,"strand":1,"description":"asparagine synthetase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39400]"}, {"versioned_ensembl_gene_id":"ENSG00000226543.3","gene_symbol":"MYL6P1","gene_name":"myosin light chain 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7588]","synonyms":"MYL6P","biotype":"processed_pseudogene","ncbi_id":"54043","summary":null,"start":43855890,"end":43856342,"strand":-1,"description":"myosin light chain 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7588]"}, {"versioned_ensembl_gene_id":"ENSG00000228984.3","gene_symbol":"AC021451.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46784800,"end":46785928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272209.1","gene_symbol":"AL023583.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13825432,"end":13826574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250857.3","gene_symbol":"TRIM60P15","gene_name":"tripartite motif containing 60 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420405","summary":null,"start":46792065,"end":46793064,"strand":1,"description":"tripartite motif containing 60 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38487]"}, {"versioned_ensembl_gene_id":"ENSG00000271249.1","gene_symbol":"DIMT1P1","gene_name":"DIM1 dimethyladenosine transferase 1 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52892]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422385","summary":null,"start":109701456,"end":109702218,"strand":-1,"description":"DIM1 dimethyladenosine transferase 1 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52892]"}, {"versioned_ensembl_gene_id":"ENSG00000249955.1","gene_symbol":"AC084866.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169981747,"end":169993806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242029.1","gene_symbol":"AC078980.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109648107,"end":109810861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214013.9","gene_symbol":"GANC","gene_name":"glucosidase alpha, neutral C [Source:HGNC Symbol;Acc:HGNC:4139]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2595","summary":"Glycosyl hydrolase enzymes hydrolyse the glycosidic bond between two or more carbohydrates, or between a carbohydrate and a non-carbohydrate moiety. This gene encodes a member of glycosyl hydrolases family 31. This enzyme hydrolyses terminal, non-reducing 1,4-linked alpha-D-glucose residues and releases alpha-D-glucose. This is a key enzyme in glycogen metabolism and its gene localizes to a chromosomal region (15q15) that is associated with susceptibility to diabetes. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2014]","start":42273233,"end":42356935,"strand":1,"description":"glucosidase alpha, neutral C [Source:HGNC Symbol;Acc:HGNC:4139]"}, {"versioned_ensembl_gene_id":"ENSG00000198948.11","gene_symbol":"MFAP3L","gene_name":"microfibril associated protein 3 like [Source:HGNC Symbol;Acc:HGNC:29083]","synonyms":"NYD-sp9,KIAA0626","biotype":"protein_coding","ncbi_id":"9848","summary":null,"start":169986597,"end":170033031,"strand":-1,"description":"microfibril associated protein 3 like [Source:HGNC Symbol;Acc:HGNC:29083]"}, {"versioned_ensembl_gene_id":"ENSG00000182866.16","gene_symbol":"LCK","gene_name":"LCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6524]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3932","summary":"This gene is a member of the Src family of protein tyrosine kinases (PTKs). The encoded protein is a key signaling molecule in the selection and maturation of developing T-cells. It contains N-terminal sites for myristylation and palmitylation, a PTK domain, and SH2 and SH3 domains which are involved in mediating protein-protein interactions with phosphotyrosine-containing and proline-rich motifs, respectively. The protein localizes to the plasma membrane and pericentrosomal vesicles, and binds to cell surface receptors, including CD4 and CD8, and other signaling molecules. Multiple alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Aug 2016]","start":32251239,"end":32286165,"strand":1,"description":"LCK proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6524]"}, {"versioned_ensembl_gene_id":"ENSG00000228612.2","gene_symbol":"HK2P1","gene_name":"hexokinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4924]","synonyms":"HK2P","biotype":"processed_pseudogene","ncbi_id":"642546","summary":null,"start":80571871,"end":80574607,"strand":-1,"description":"hexokinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4924]"}, {"versioned_ensembl_gene_id":"ENSG00000250214.1","gene_symbol":"AC112225.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77864508,"end":77864804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166573.5","gene_symbol":"GALR1","gene_name":"galanin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4132]","synonyms":"GALNR,GALNR1","biotype":"protein_coding","ncbi_id":"2587","summary":"The neuropeptide galanin elicits a range of biological effects by interaction with specific G-protein-coupled receptors. Galanin receptors are seven-transmembrane proteins shown to activate a variety of intracellular second-messenger pathways. GALR1 inhibits adenylyl cyclase via a G protein of the Gi/Go family. GALR1 is widely expressed in the brain and spinal cord, as well as in peripheral sites such as the small intestine and heart. [provided by RefSeq, Jul 2008]","start":77250549,"end":77277896,"strand":1,"description":"galanin receptor 1 [Source:HGNC Symbol;Acc:HGNC:4132]"}, {"versioned_ensembl_gene_id":"ENSG00000136715.17","gene_symbol":"SAP130","gene_name":"Sin3A associated protein 130 [Source:HGNC Symbol;Acc:HGNC:29813]","synonyms":"FLJ12761","biotype":"protein_coding","ncbi_id":"79595","summary":"SAP130 is a subunit of the histone deacetylase (see HDAC1; MIM 601241)-dependent SIN3A (MIM 607776) corepressor complex (Fleischer et al., 2003 [PubMed 12724404]).[supplied by OMIM, Mar 2008]","start":127941217,"end":128028120,"strand":-1,"description":"Sin3A associated protein 130 [Source:HGNC Symbol;Acc:HGNC:29813]"}, {"versioned_ensembl_gene_id":"ENSG00000251451.1","gene_symbol":"GTF2IP9","gene_name":"general transcription factor IIi pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51721]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106481734","summary":null,"start":66407288,"end":66409239,"strand":-1,"description":"general transcription factor IIi pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51721]"}, {"versioned_ensembl_gene_id":"ENSG00000157741.14","gene_symbol":"UBN2","gene_name":"ubinuclein 2 [Source:HGNC Symbol;Acc:HGNC:21931]","synonyms":"KIAA2030,FLJ25778","biotype":"protein_coding","ncbi_id":"254048","summary":null,"start":139230356,"end":139308236,"strand":1,"description":"ubinuclein 2 [Source:HGNC Symbol;Acc:HGNC:21931]"}, {"versioned_ensembl_gene_id":"ENSG00000230189.7","gene_symbol":"AC008267.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66427949,"end":66453634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105612.8","gene_symbol":"DNASE2","gene_name":"deoxyribonuclease 2, lysosomal [Source:HGNC Symbol;Acc:HGNC:2960]","synonyms":"DNL2,DNL","biotype":"protein_coding","ncbi_id":"1777","summary":"This gene encodes a member of the DNase family. The protein, located in the lysosome, hydrolyzes DNA under acidic conditions and mediates the breakdown of DNA during erythropoiesis and apoptosis. Two codominant alleles have been characterized, DNASE2*L (low activity) and DNASE2*H (high activity), that differ at one nucleotide in the promoter region. The DNASE2*H allele is represented in this record. [provided by RefSeq, Jul 2008]","start":12875211,"end":12881468,"strand":-1,"description":"deoxyribonuclease 2, lysosomal [Source:HGNC Symbol;Acc:HGNC:2960]"}, {"versioned_ensembl_gene_id":"ENSG00000169902.13","gene_symbol":"TPST1","gene_name":"tyrosylprotein sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:12020]","synonyms":"TANGO13A","biotype":"protein_coding","ncbi_id":"8460","summary":null,"start":66205199,"end":66420543,"strand":1,"description":"tyrosylprotein sulfotransferase 1 [Source:HGNC Symbol;Acc:HGNC:12020]"}, {"versioned_ensembl_gene_id":"ENSG00000275699.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803535,"end":54814517,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000280782.1","gene_symbol":"MRPS16P3","gene_name":"mitochondrial ribosomal protein S16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29733]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338388","summary":null,"start":35703803,"end":35704176,"strand":1,"description":"mitochondrial ribosomal protein S16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29733]"}, {"versioned_ensembl_gene_id":"ENSG00000259156.7","gene_symbol":"CHEK2P2","gene_name":"checkpoint kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43578]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646096","summary":null,"start":20282744,"end":20291586,"strand":1,"description":"checkpoint kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43578]"}, {"versioned_ensembl_gene_id":"ENSG00000282183.1","gene_symbol":"GOLGA2P10","gene_name":"golgin A2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:26229]","synonyms":"FLJ22795,AgSK1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"80154","summary":null,"start":82552056,"end":82593266,"strand":-1,"description":"golgin A2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:26229]"}, {"versioned_ensembl_gene_id":"ENSG00000278726.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850439,"end":54867235,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000228291.1","gene_symbol":"ARL4AP3","gene_name":"ADP ribosylation factor like GTPase 4A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52372]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107984161","summary":null,"start":5207169,"end":5207742,"strand":1,"description":"ADP ribosylation factor like GTPase 4A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52372]"}, {"versioned_ensembl_gene_id":"ENSG00000189060.5","gene_symbol":"H1F0","gene_name":"H1 histone family member 0 [Source:HGNC Symbol;Acc:HGNC:4714]","synonyms":"H10,H1FV","biotype":"protein_coding","ncbi_id":"3005","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-independent histone that is a member of the histone H1 family. [provided by RefSeq, Oct 2015]","start":37805093,"end":37807436,"strand":1,"description":"H1 histone family member 0 [Source:HGNC Symbol;Acc:HGNC:4714]"}, {"versioned_ensembl_gene_id":"ENSG00000183310.3","gene_symbol":"OR2T34","gene_name":"olfactory receptor family 2 subfamily T member 34 [Source:HGNC Symbol;Acc:HGNC:31256]","synonyms":null,"biotype":"protein_coding","ncbi_id":"127068","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248573801,"end":248574757,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 34 [Source:HGNC Symbol;Acc:HGNC:31256]"}, {"versioned_ensembl_gene_id":"ENSG00000276379.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,CD158e1/2,nkat3,NKB1,CD158e2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816496,"end":54820397,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000230000.2","gene_symbol":"AC006455.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63348861,"end":63351774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151725.11","gene_symbol":"CENPU","gene_name":"centromere protein U [Source:HGNC Symbol;Acc:HGNC:21348]","synonyms":"PBIP1,MLF1IP,KLIP1,CENP-U,CENP-50","biotype":"protein_coding","ncbi_id":"79682","summary":"The centromere is a specialized chromatin domain, present throughout the cell cycle, that acts as a platform on which the transient assembly of the kinetochore occurs during mitosis. All active centromeres are characterized by the presence of long arrays of nucleosomes in which CENPA (MIM 117139) replaces histone H3 (see MIM 601128). MLF1IP, or CENPU, is an additional factor required for centromere assembly (Foltz et al., 2006 [PubMed 16622419]).[supplied by OMIM, Mar 2008]","start":184694618,"end":184734133,"strand":-1,"description":"centromere protein U [Source:HGNC Symbol;Acc:HGNC:21348]"}, {"versioned_ensembl_gene_id":"ENSG00000226851.1","gene_symbol":"AC004112.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112328189,"end":112409623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155016.17","gene_symbol":"CYP2U1","gene_name":"cytochrome P450 family 2 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:20582]","synonyms":"SPG49","biotype":"protein_coding","ncbi_id":"113612","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a hydroxylase that metabolizes arachidonic acid, docosahexaenoic acid, and other long chain fatty acids. [provided by RefSeq, Jul 2008]","start":107931369,"end":107953457,"strand":1,"description":"cytochrome P450 family 2 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:20582]"}, {"versioned_ensembl_gene_id":"ENSG00000224883.1","gene_symbol":"Z99716.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41981304,"end":41982217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237076.1","gene_symbol":"AL035706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83790280,"end":83801465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256283.1","gene_symbol":"METTL8P1","gene_name":"methyltransferase like 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49856]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728996","summary":null,"start":15255213,"end":15255823,"strand":-1,"description":"methyltransferase like 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49856]"}, {"versioned_ensembl_gene_id":"ENSG00000206455.8","gene_symbol":"TCF19","gene_name":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]","synonyms":"SC1","biotype":"protein_coding","ncbi_id":"6941","summary":"This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31150981,"end":31156655,"strand":1,"description":"transcription factor 19 [Source:HGNC Symbol;Acc:HGNC:11629]"}, {"versioned_ensembl_gene_id":"ENSG00000228144.2","gene_symbol":"AC078927.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66123917,"end":66169985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279705.1","gene_symbol":"AC092701.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80014157,"end":80015707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064205.10","gene_symbol":"WISP2","gene_name":"WNT1 inducible signaling pathway protein 2 [Source:HGNC Symbol;Acc:HGNC:12770]","synonyms":"CCN5,CTGF-L,CT58","biotype":"protein_coding","ncbi_id":"8839","summary":"This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like (CT) domain. The encoded protein lacks the CT domain which is implicated in dimerization and heparin binding. It is 72% identical to the mouse protein at the amino acid level. This gene may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Its expression in colon tumors is reduced while the other two WISP members are overexpressed in colon tumors. It is expressed at high levels in bone tissue, and may play an important role in modulating bone turnover. [provided by RefSeq, Jul 2008]","start":44714844,"end":44728509,"strand":1,"description":"WNT1 inducible signaling pathway protein 2 [Source:HGNC Symbol;Acc:HGNC:12770]"}, {"versioned_ensembl_gene_id":"ENSG00000124249.6","gene_symbol":"KCNK15","gene_name":"potassium two pore domain channel subfamily K member 15 [Source:HGNC Symbol;Acc:HGNC:13814]","synonyms":"KIAA0237,KCNK14,KCNK11,K2p15.1,dJ781B1.1,TASK5,TASK-5,KT3.3","biotype":"protein_coding","ncbi_id":"60598","summary":"This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008]","start":44745780,"end":44752313,"strand":1,"description":"potassium two pore domain channel subfamily K member 15 [Source:HGNC Symbol;Acc:HGNC:13814]"}, {"versioned_ensembl_gene_id":"ENSG00000280282.1","gene_symbol":"AC138430.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19255638,"end":19256141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104899.7","gene_symbol":"AMH","gene_name":"anti-Mullerian hormone [Source:HGNC Symbol;Acc:HGNC:464]","synonyms":"MIS","biotype":"protein_coding","ncbi_id":"268","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate N- and C-terminal cleavage products that homodimerize and associate to form a biologically active noncovalent complex. This complex binds to the anti-Mullerian hormone receptor type 2 and causes the regression of Mullerian ducts in the male embryo that would otherwise differentiate into the uterus and fallopian tubes. This protein also plays a role in Leydig cell differentiation and function and follicular development in adult females. Mutations in this gene result in persistent Mullerian duct syndrome. [provided by RefSeq, Jul 2016]","start":2249309,"end":2252073,"strand":1,"description":"anti-Mullerian hormone [Source:HGNC Symbol;Acc:HGNC:464]"}, {"versioned_ensembl_gene_id":"ENSG00000233064.2","gene_symbol":"AL136307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5851506,"end":5870220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187105.8","gene_symbol":"HEATR4","gene_name":"HEAT repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:16761]","synonyms":"MGC48595","biotype":"protein_coding","ncbi_id":"399671","summary":null,"start":73478484,"end":73558947,"strand":-1,"description":"HEAT repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:16761]"}, {"versioned_ensembl_gene_id":"ENSG00000255072.1","gene_symbol":"PIGY","gene_name":"phosphatidylinositol glycan anchor biosynthesis class Y [Source:HGNC Symbol;Acc:HGNC:28213]","synonyms":"MGC14156","biotype":"protein_coding","ncbi_id":"84992","summary":"The protein encoded by this gene is part of the GPI-N-acetylglucosaminyltransferase (GIP-GnT) complex which initiates the biosynthesis of glycosylphosphatidylinositol (GPI). GPI is synthesized in the endoplasmic reticulum and serves as an anchor for many surface proteins. Proteins containing GPI anchors can have an important role in cell-cell interactions. The transcript for this gene is bicistronic. The downstream open reading frame encodes this GPI-GnT complex protein, while the upstream open reading frame encodes a protein with unknown function, as represented by GeneID:100996939. [provided by RefSeq, Aug 2012]","start":88521573,"end":88521789,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class Y [Source:HGNC Symbol;Acc:HGNC:28213]"}, {"versioned_ensembl_gene_id":"ENSG00000232524.1","gene_symbol":"AC073323.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123456629,"end":123459856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222032.1","gene_symbol":"AC112721.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237428920,"end":237434822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273507.4","gene_symbol":"AL354809.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39053072,"end":39221927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245651.2","gene_symbol":"AC083805.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57869835,"end":57896482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242411.2","gene_symbol":"AC011506.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56217168,"end":56217777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234148.2","gene_symbol":"LINC01961","gene_name":"long intergenic non-protein coding RNA 1961 [Source:HGNC Symbol;Acc:HGNC:52786]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927424","summary":null,"start":113512463,"end":113515485,"strand":1,"description":"long intergenic non-protein coding RNA 1961 [Source:HGNC Symbol;Acc:HGNC:52786]"}, {"versioned_ensembl_gene_id":"ENSG00000231943.7","gene_symbol":"PGM5P4-AS1","gene_name":"PGM5P4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51195]","synonyms":"FAM233C","biotype":"lincRNA","ncbi_id":"103344932","summary":null,"start":113527568,"end":113542672,"strand":-1,"description":"PGM5P4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51195]"}, {"versioned_ensembl_gene_id":"ENSG00000168806.7","gene_symbol":"LCMT2","gene_name":"leucine carboxyl methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:17558]","synonyms":"TYW4,PPM2,MGC9534,KIAA0547","biotype":"protein_coding","ncbi_id":"9836","summary":"The protein encoded by this intronless gene belongs to the highly variable methyltransferase superfamily. This gene is the inferred homolog of the Saccharomyces cerevisiae carboxymethyltransferase gene PPM2 that is essential for the synthesis of the hypermodified guanosine Wybutosine (yW). [provided by RefSeq, Jul 2008]","start":43323649,"end":43330605,"strand":-1,"description":"leucine carboxyl methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:17558]"}, {"versioned_ensembl_gene_id":"ENSG00000184492.6","gene_symbol":"FOXD4L1","gene_name":"forkhead box D4 like 1 [Source:HGNC Symbol;Acc:HGNC:18521]","synonyms":"FOXD5","biotype":"protein_coding","ncbi_id":"200350","summary":"This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008]","start":113498665,"end":113501155,"strand":1,"description":"forkhead box D4 like 1 [Source:HGNC Symbol;Acc:HGNC:18521]"}, {"versioned_ensembl_gene_id":"ENSG00000267332.1","gene_symbol":"BOLA3P2","gene_name":"bolA family member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51441]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287463","summary":null,"start":9019344,"end":9019984,"strand":1,"description":"bolA family member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51441]"}, {"versioned_ensembl_gene_id":"ENSG00000074657.13","gene_symbol":"ZNF532","gene_name":"zinc finger protein 532 [Source:HGNC Symbol;Acc:HGNC:30940]","synonyms":"FLJ10697","biotype":"protein_coding","ncbi_id":"55205","summary":null,"start":58862600,"end":58986480,"strand":1,"description":"zinc finger protein 532 [Source:HGNC Symbol;Acc:HGNC:30940]"}, {"versioned_ensembl_gene_id":"ENSG00000263331.1","gene_symbol":"AC008551.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21120758,"end":21130108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275851.4","gene_symbol":"MLLT6","gene_name":"MLLT6, PHD finger containing [Source:HGNC Symbol;Acc:HGNC:7138]","synonyms":"FLJ23480,AF17","biotype":"protein_coding","ncbi_id":"4302","summary":null,"start":38506329,"end":38530590,"strand":1,"description":"MLLT6, PHD finger containing [Source:HGNC Symbol;Acc:HGNC:7138]"}, {"versioned_ensembl_gene_id":"ENSG00000214998.2","gene_symbol":"CCNB2P1","gene_name":"cyclin B2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50850]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132073","summary":null,"start":7909300,"end":7910449,"strand":-1,"description":"cyclin B2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50850]"}, {"versioned_ensembl_gene_id":"ENSG00000235029.1","gene_symbol":"MNX1-AS2","gene_name":"MNX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40278]","synonyms":"ENST00000429228","biotype":"antisense_RNA","ncbi_id":"105375606","summary":null,"start":157006307,"end":157007132,"strand":1,"description":"MNX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40278]"}, {"versioned_ensembl_gene_id":"ENSG00000140937.13","gene_symbol":"CDH11","gene_name":"cadherin 11 [Source:HGNC Symbol;Acc:HGNC:1750]","synonyms":"OB,CAD11","biotype":"protein_coding","ncbi_id":"1009","summary":"This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. Expression of this particular cadherin in osteoblastic cell lines, and its upregulation during differentiation, suggests a specific function in bone development and maintenance. [provided by RefSeq, Jul 2008]","start":64943753,"end":65126112,"strand":-1,"description":"cadherin 11 [Source:HGNC Symbol;Acc:HGNC:1750]"}, {"versioned_ensembl_gene_id":"ENSG00000228198.3","gene_symbol":"OR2M3","gene_name":"olfactory receptor family 2 subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:8269]","synonyms":"OST003,OR2M6,OR2M3P","biotype":"protein_coding","ncbi_id":"127062","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248197265,"end":248212925,"strand":1,"description":"olfactory receptor family 2 subfamily M member 3 [Source:HGNC Symbol;Acc:HGNC:8269]"}, {"versioned_ensembl_gene_id":"ENSG00000282151.1","gene_symbol":"IGHV3-43","gene_name":"immunoglobulin heavy variable 3-43 [Source:HGNC Symbol;Acc:HGNC:5604]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28426","summary":null,"start":106494944,"end":106495481,"strand":-1,"description":"immunoglobulin heavy variable 3-43 [Source:HGNC Symbol;Acc:HGNC:5604]"}, {"versioned_ensembl_gene_id":"ENSG00000242044.1","gene_symbol":"CR933859.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32690660,"end":32693255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254366.6","gene_symbol":"AC062004.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77399072,"end":77537290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253952.1","gene_symbol":"HIGD1AP18","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:43013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874456","summary":null,"start":77013751,"end":77014028,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:43013]"}, {"versioned_ensembl_gene_id":"ENSG00000267204.1","gene_symbol":"LINC01782","gene_name":"long intergenic non-protein coding RNA 1782 [Source:HGNC Symbol;Acc:HGNC:52572]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927411","summary":null,"start":32102088,"end":32105916,"strand":-1,"description":"long intergenic non-protein coding RNA 1782 [Source:HGNC Symbol;Acc:HGNC:52572]"}, {"versioned_ensembl_gene_id":"ENSG00000255502.5","gene_symbol":"AP003730.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97878781,"end":97942762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136371.10","gene_symbol":"MTHFS","gene_name":"methenyltetrahydrofolate synthetase [Source:HGNC Symbol;Acc:HGNC:7437]","synonyms":"HsT19268","biotype":"protein_coding","ncbi_id":"10588","summary":"The protein encoded by this gene is an enzyme that catalyzes the conversion of 5-formyltetrahydrofolate to 5,10-methenyltetrahydrofolate, a precursor of reduced folates involved in 1-carbon metabolism. An increased activity of the encoded protein can result in an increased folate turnover rate and folate depletion. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":79833585,"end":79897379,"strand":-1,"description":"methenyltetrahydrofolate synthetase [Source:HGNC Symbol;Acc:HGNC:7437]"}, {"versioned_ensembl_gene_id":"ENSG00000249006.1","gene_symbol":"AL136360.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2088718,"end":2090617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181143.15","gene_symbol":"MUC16","gene_name":"mucin 16, cell surface associated [Source:HGNC Symbol;Acc:HGNC:15582]","synonyms":"FLJ14303,CA125","biotype":"protein_coding","ncbi_id":"94025","summary":"This gene encodes a protein that is a member of the mucin family. Mucins are high molecular weight, O-glycosylated proteins that play an important role in forming a protective mucous barrier, and are found on the apical surfaces of the epithelia. The encoded protein is a membrane-tethered mucin that contains an extracellular domain at its amino terminus, a large tandem repeat domain, and a transmembrane domain with a short cytoplasmic domain. The amino terminus is highly glycosylated, while the repeat region contains 156 amino acid repeats unit that are rich in serines, threonines, and prolines. Interspersed within the repeats are Sea urchin sperm protein Enterokinase and Agrin (SEA) modules, leucine-rich repeats and ankyrin (ANK) repeats. These regions together form the ectodomain, and there is a potential cleavage site found near an SEA module close to the transmembrane domain. This protein is thought to play a role in forming a barrier, protecting epithelial cells from pathogens. Products of this gene have been used as a marker for different cancers, with higher expression levels associated with poorer outcomes. [provided by RefSeq, May 2017]","start":8848844,"end":8981342,"strand":-1,"description":"mucin 16, cell surface associated [Source:HGNC Symbol;Acc:HGNC:15582]"}, {"versioned_ensembl_gene_id":"ENSG00000248965.1","gene_symbol":"AC011389.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168993000,"end":168995677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151062.14","gene_symbol":"CACNA2D4","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 4 [Source:HGNC Symbol;Acc:HGNC:20202]","synonyms":null,"biotype":"protein_coding","ncbi_id":"93589","summary":"This gene encodes a member of the alpha-2/delta subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Various versions of each of these subunits exist, either expressed from similar genes or the result of alternative splicing. Research on a highly similar protein in rabbit suggests the protein described in this record is cleaved into alpha-2 and delta subunits. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":1791957,"end":1918836,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit alpha2delta 4 [Source:HGNC Symbol;Acc:HGNC:20202]"}, {"versioned_ensembl_gene_id":"ENSG00000280105.1","gene_symbol":"AC009487.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":161433874,"end":161437458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244722.1","gene_symbol":"RPSAP29","gene_name":"ribosomal protein SA pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36680]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389141","summary":null,"start":110682286,"end":110683154,"strand":-1,"description":"ribosomal protein SA pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36680]"}, {"versioned_ensembl_gene_id":"ENSG00000259954.1","gene_symbol":"IL21R-AS1","gene_name":"IL21R antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27551]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283888","summary":null,"start":27447669,"end":27453393,"strand":-1,"description":"IL21R antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27551]"}, {"versioned_ensembl_gene_id":"ENSG00000257884.2","gene_symbol":"AL512310.7","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":19677837,"end":19680104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023892.10","gene_symbol":"DEF6","gene_name":"DEF6, guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:2760]","synonyms":"SWAP70L,SLAT,IBP","biotype":"protein_coding","ncbi_id":"50619","summary":"DEF6, or IBP, is a guanine nucleotide exchange factor (GEF) for RAC (MIM 602048) and CDC42 (MIM 116952) that is highly expressed in B and T cells (Gupta et al., 2003 [PubMed 12923183]).[supplied by OMIM, Mar 2008]","start":35297852,"end":35321771,"strand":1,"description":"DEF6, guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:2760]"}, {"versioned_ensembl_gene_id":"ENSG00000152359.14","gene_symbol":"POC5","gene_name":"POC5 centriolar protein [Source:HGNC Symbol;Acc:HGNC:26658]","synonyms":"MGC120444,MGC120443,MGC120442,hPOC5,FLJ35779,C5orf37","biotype":"protein_coding","ncbi_id":"134359","summary":null,"start":75674124,"end":75717481,"strand":-1,"description":"POC5 centriolar protein [Source:HGNC Symbol;Acc:HGNC:26658]"}, {"versioned_ensembl_gene_id":"ENSG00000224743.6","gene_symbol":"TEX26-AS1","gene_name":"TEX26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42784]","synonyms":"LINC00447","biotype":"antisense_RNA","ncbi_id":"100507064","summary":null,"start":30881933,"end":30933846,"strand":-1,"description":"TEX26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42784]"}, {"versioned_ensembl_gene_id":"ENSG00000253401.1","gene_symbol":"VTA1P2","gene_name":"vesicle trafficking 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50484]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128412","summary":null,"start":87575598,"end":87576508,"strand":-1,"description":"vesicle trafficking 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50484]"}, {"versioned_ensembl_gene_id":"ENSG00000196839.12","gene_symbol":"ADA","gene_name":"adenosine deaminase [Source:HGNC Symbol;Acc:HGNC:186]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100","summary":"This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine in the purine catabolic pathway. Various mutations have been described for this gene and have been linked to human diseases related to impaired immune function such as severe combined immunodeficiency disease (SCID) which is the result of a deficiency in the ADA enzyme. In ADA-deficient individuals there is a marked depletion of T, B, and NK lymphocytes, and consequently, a lack of both humoral and cellular immunity. Conversely, elevated levels of this enzyme are associated with congenital hemolytic anemia. [provided by RefSeq, Sep 2019]","start":44619522,"end":44652233,"strand":-1,"description":"adenosine deaminase [Source:HGNC Symbol;Acc:HGNC:186]"}, {"versioned_ensembl_gene_id":"ENSG00000273666.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000219784.2","gene_symbol":"AL138729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121478273,"end":121479908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259342.1","gene_symbol":"AC025580.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45430652,"end":45441808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231296.1","gene_symbol":"AL050341.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40262672,"end":40262984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254192.1","gene_symbol":"AC011365.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168654513,"end":168667761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279752.1","gene_symbol":"AC011389.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":169012148,"end":169013146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271270.5","gene_symbol":"TMCC1-AS1","gene_name":"TMCC1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49060]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507032","summary":null,"start":129893871,"end":129918575,"strand":1,"description":"TMCC1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49060]"}, {"versioned_ensembl_gene_id":"ENSG00000235837.1","gene_symbol":"AC073333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16695871,"end":16719898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125522.3","gene_symbol":"NPBWR2","gene_name":"neuropeptides B and W receptor 2 [Source:HGNC Symbol;Acc:HGNC:4530]","synonyms":"GPR8","biotype":"protein_coding","ncbi_id":"2832","summary":"The protein encoded by this gene is an integral membrane protein and G protein-coupled receptor. The encoded protein is similar in sequence to another G protein-coupled receptor (GPR7), and it is structurally similar to opioid and somatostatin receptors. This protein binds neuropeptides B and W. This gene is intronless and is expressed primarily in the frontal cortex of the brain. [provided by RefSeq, Jul 2008]","start":64105820,"end":64107171,"strand":-1,"description":"neuropeptides B and W receptor 2 [Source:HGNC Symbol;Acc:HGNC:4530]"}, {"versioned_ensembl_gene_id":"ENSG00000269400.1","gene_symbol":"AC008734.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8833065,"end":8833541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180803.3","gene_symbol":"AL157366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25863250,"end":25863667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229261.1","gene_symbol":"AL596223.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69215333,"end":69232490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163734.4","gene_symbol":"CXCL3","gene_name":"C-X-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:4604]","synonyms":"GRO3,CINC-2b,SCYB3,MIP-2b,GROg","biotype":"protein_coding","ncbi_id":"2921","summary":"This antimicrobial gene encodes a member of the CXC subfamily of chemokines. The encoded protein is a secreted growth factor that signals through the G-protein coupled receptor, CXC receptor 2. This protein plays a role in inflammation and as a chemoattractant for neutrophils. [provided by RefSeq, Sep 2014]","start":74036589,"end":74038807,"strand":-1,"description":"C-X-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:4604]"}, {"versioned_ensembl_gene_id":"ENSG00000261002.5","gene_symbol":"AC036103.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42208413,"end":42226990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277945.1","gene_symbol":"AC107308.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65830750,"end":65831050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147570.9","gene_symbol":"DNAJC5B","gene_name":"DnaJ heat shock protein family (Hsp40) member C5 beta [Source:HGNC Symbol;Acc:HGNC:24138]","synonyms":"MGC26226,CSP-beta","biotype":"protein_coding","ncbi_id":"85479","summary":"This gene encodes a member of the DNAJ heat shock protein 40 family of co-chaperone proteins that is characterized by an N-terminal DNAJ domain, a linker region, and a cysteine-rich C-terminal domain. The encoded protein, together with heat shock protein 70, is thought to regulate the proper folding of other proteins. The orthologous mouse protein is membrane-associated and is targeted to the trans-golgi network. [provided by RefSeq, Mar 2017]","start":66021560,"end":66100526,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C5 beta [Source:HGNC Symbol;Acc:HGNC:24138]"}, {"versioned_ensembl_gene_id":"ENSG00000270268.1","gene_symbol":"AL009028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79369364,"end":79370165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275368.2","gene_symbol":"TCTE3","gene_name":"t-complex-associated-testis-expressed 3 [Source:HGNC Symbol;Acc:HGNC:11695]","synonyms":"TCTEX1D3","biotype":"protein_coding","ncbi_id":"6991","summary":null,"start":169740114,"end":169751587,"strand":-1,"description":"t-complex-associated-testis-expressed 3 [Source:HGNC Symbol;Acc:HGNC:11695]"}, {"versioned_ensembl_gene_id":"ENSG00000282623.1","gene_symbol":"AL078601.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79434072,"end":79434606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232775.6","gene_symbol":"BMS1P22","gene_name":"BMS1, ribosome biogenesis factor pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51603]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106480334","summary":null,"start":15805263,"end":15820884,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:51603]"}, {"versioned_ensembl_gene_id":"ENSG00000271127.1","gene_symbol":"AP000526.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":15796959,"end":15798346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273741.1","gene_symbol":"AL078601.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79448129,"end":79449137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266846.1","gene_symbol":"AP001021.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6025091,"end":6082455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269300.1","gene_symbol":"AC008734.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8821501,"end":8824110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089472.16","gene_symbol":"HEPH","gene_name":"hephaestin [Source:HGNC Symbol;Acc:HGNC:4866]","synonyms":"KIAA0698,CPL","biotype":"protein_coding","ncbi_id":"9843","summary":"This gene encodes a member of the multicopper oxidase protein family. The encoded protein is involved in the transport of dietary iron from epithelial cells of the intestinal lumen into the circulatory system, and may be involved in copper transport and homeostasis. In mouse, defects in this gene can lead to severe microcytic anemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":66162549,"end":66268867,"strand":1,"description":"hephaestin [Source:HGNC Symbol;Acc:HGNC:4866]"}, {"versioned_ensembl_gene_id":"ENSG00000274489.1","gene_symbol":"AC124076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36795255,"end":36795862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224173.1","gene_symbol":"AC007422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67562067,"end":67574044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271005.1","gene_symbol":"CTHRC1P1","gene_name":"collagen triple helix repeat containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50463]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480299","summary":null,"start":79177200,"end":79177668,"strand":-1,"description":"collagen triple helix repeat containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50463]"}, {"versioned_ensembl_gene_id":"ENSG00000169439.11","gene_symbol":"SDC2","gene_name":"syndecan 2 [Source:HGNC Symbol;Acc:HGNC:10659]","synonyms":"SYND2,HSPG1,HSPG,fibroglycan,CD362","biotype":"protein_coding","ncbi_id":"6383","summary":"The protein encoded by this gene is a transmembrane (type I) heparan sulfate proteoglycan and is a member of the syndecan proteoglycan family. The syndecans mediate cell binding, cell signaling, and cytoskeletal organization and syndecan receptors are required for internalization of the HIV-1 tat protein. The syndecan-2 protein functions as an integral membrane protein and participates in cell proliferation, cell migration and cell-matrix interactions via its receptor for extracellular matrix proteins. Altered syndecan-2 expression has been detected in several different tumor types. [provided by RefSeq, Jul 2008]","start":96493351,"end":96611780,"strand":1,"description":"syndecan 2 [Source:HGNC Symbol;Acc:HGNC:10659]"}, {"versioned_ensembl_gene_id":"ENSG00000254187.1","gene_symbol":"AC008708.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167653228,"end":167660481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228260.2","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206E,HLA-DRB1L,D6S206,HLA-DR1BL","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32535112,"end":32548767,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000253527.1","gene_symbol":"AC008601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167306273,"end":167309870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237410.1","gene_symbol":"AP001092.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64646399,"end":64659681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149260.15","gene_symbol":"CAPN5","gene_name":"calpain 5 [Source:HGNC Symbol;Acc:HGNC:1482]","synonyms":"VRNI,nCL-3,HTRA3,ADNIV","biotype":"protein_coding","ncbi_id":"726","summary":"Calpains are calcium-dependent cysteine proteases involved in signal transduction in a variety of cellular processes. A functional calpain protein consists of an invariant small subunit and 1 of a family of large subunits. CAPN5 is one of the large subunits. Unlike some of the calpains, CAPN5 and CAPN6 lack a calmodulin-like domain IV. Because of the significant similarity to Caenorhabditis elegans sex determination gene tra-3, CAPN5 is also called as HTRA3. [provided by RefSeq, Jul 2008]","start":77066932,"end":77126155,"strand":1,"description":"calpain 5 [Source:HGNC Symbol;Acc:HGNC:1482]"}, {"versioned_ensembl_gene_id":"ENSG00000276287.1","gene_symbol":"AC012314.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54200068,"end":54200585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279426.1","gene_symbol":"AC243312.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8695721,"end":8696321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233634.1","gene_symbol":"GOT2P5","gene_name":"glutamic-oxaloacetic transaminase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38439]","synonyms":"GOT2Y","biotype":"processed_pseudogene","ncbi_id":"100422625","summary":null,"start":6837707,"end":6838252,"strand":1,"description":"glutamic-oxaloacetic transaminase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38439]"}, {"versioned_ensembl_gene_id":"ENSG00000272948.2","gene_symbol":"AP001412.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37267784,"end":37268497,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275131.2","gene_symbol":"AC241952.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":120489860,"end":120701289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227303.1","gene_symbol":"AC239727.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143284977,"end":143516803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124406.16","gene_symbol":"ATP8A1","gene_name":"ATPase phospholipid transporting 8A1 [Source:HGNC Symbol;Acc:HGNC:13531]","synonyms":"ATPIA","biotype":"protein_coding","ncbi_id":"10396","summary":"The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily catalyzes transport of heavy metal ions. Another subfamily transports non-heavy metal ions (NMHI). The protein encoded by this gene is a member of the third subfamily of P-type ATPases and acts to transport amphipaths, such as phosphatidylserine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":42408373,"end":42657105,"strand":-1,"description":"ATPase phospholipid transporting 8A1 [Source:HGNC Symbol;Acc:HGNC:13531]"}, {"versioned_ensembl_gene_id":"ENSG00000272361.2","gene_symbol":"AC005014.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16593626,"end":16594224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257506.1","gene_symbol":"AC133555.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29478879,"end":29482591,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275522.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814247,"end":54828575,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000203623.4","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"D6S53E,G4","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31648523,"end":31650997,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000254585.2","gene_symbol":"MAGEL2","gene_name":"MAGE family member L2 [Source:HGNC Symbol;Acc:HGNC:6814]","synonyms":"nM15,NDNL1","biotype":"protein_coding","ncbi_id":"54551","summary":"Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]","start":23643544,"end":23647841,"strand":-1,"description":"MAGE family member L2 [Source:HGNC Symbol;Acc:HGNC:6814]"}, {"versioned_ensembl_gene_id":"ENSG00000179222.17","gene_symbol":"MAGED1","gene_name":"MAGE family member D1 [Source:HGNC Symbol;Acc:HGNC:6813]","synonyms":"NRAGE,DLXIN-1","biotype":"protein_coding","ncbi_id":"9500","summary":"This gene is a member of the melanoma antigen gene (MAGE) family. Most of the genes of this family encode tumor specific antigens that are not expressed in normal adult tissues except testis. Although the protein encoded by this gene shares strong homology with members of the MAGE family, it is expressed in almost all normal adult tissues. This gene has been demonstrated to be involved in the p75 neurotrophin receptor mediated programmed cell death pathway. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":51803007,"end":51902357,"strand":1,"description":"MAGE family member D1 [Source:HGNC Symbol;Acc:HGNC:6813]"}, {"versioned_ensembl_gene_id":"ENSG00000257222.1","gene_symbol":"AC079907.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102063355,"end":102074820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234421.2","gene_symbol":"SLC25A5P4","gene_name":"solute carrier family 25 member 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35471]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131027","summary":null,"start":57314739,"end":57315909,"strand":1,"description":"solute carrier family 25 member 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35471]"}, {"versioned_ensembl_gene_id":"ENSG00000275508.1","gene_symbol":"AL109620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":142372276,"end":142373990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271209.1","gene_symbol":"BRDTP1","gene_name":"bromodomain testis associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51447]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643486","summary":null,"start":96337236,"end":96337912,"strand":-1,"description":"bromodomain testis associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51447]"}, {"versioned_ensembl_gene_id":"ENSG00000232069.1","gene_symbol":"RPS29P28","gene_name":"ribosomal protein S29 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36830]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271402","summary":null,"start":96195477,"end":96195617,"strand":1,"description":"ribosomal protein S29 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36830]"}, {"versioned_ensembl_gene_id":"ENSG00000231461.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33091753,"end":33097295,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000281861.1","gene_symbol":"SLC9A3","gene_name":"solute carrier family 9 member A3 [Source:HGNC Symbol;Acc:HGNC:11073]","synonyms":"NHE3","biotype":"protein_coding","ncbi_id":"6550","summary":"The protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22. [provided by RefSeq, Mar 2016]","start":524112,"end":524332,"strand":-1,"description":"solute carrier family 9 member A3 [Source:HGNC Symbol;Acc:HGNC:11073]"}, {"versioned_ensembl_gene_id":"ENSG00000228319.1","gene_symbol":"SPATA2P1","gene_name":"spermatogenesis associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39446]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873966","summary":null,"start":56214373,"end":56216942,"strand":1,"description":"spermatogenesis associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39446]"}, {"versioned_ensembl_gene_id":"ENSG00000261662.1","gene_symbol":"AL359752.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":119909255,"end":119910613,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183853.17","gene_symbol":"KIRREL1","gene_name":"kirre like nephrin family adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:15734]","synonyms":"NEPH1,KIRREL","biotype":"protein_coding","ncbi_id":"55243","summary":"NEPH1 is a member of the nephrin-like protein family, which includes NEPH2 (MIM 607761) and NEPH3 (MIM 607762). The cytoplasmic domains of these proteins interact with the C terminus of podocin (NPHS2; MIM 604766), and the genes are expressed in kidney podocytes, cells involved in ensuring size- and charge-selective ultrafiltration (Sellin et al., 2003 [PubMed 12424224]).[supplied by OMIM, Mar 2008]","start":157993273,"end":158100262,"strand":1,"description":"kirre like nephrin family adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:15734]"}, {"versioned_ensembl_gene_id":"ENSG00000217179.1","gene_symbol":"MTCYBP2","gene_name":"mitochondrially encoded cytochrome b pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38807]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873168","summary":null,"start":18872102,"end":18872272,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38807]"}, {"versioned_ensembl_gene_id":"ENSG00000132466.18","gene_symbol":"ANKRD17","gene_name":"ankyrin repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:23575]","synonyms":"NY-BR-16,MASK2,KIAA0697,GTAR,FLJ22206","biotype":"protein_coding","ncbi_id":"26057","summary":"The protein encoded by this gene belongs to the family of ankyrin repeat-containing proteins, and contains two distinct arrays of ankyrin repeats in its amino-terminal region, one with 15 ankyrin repeats, and the other with 10 ankyrin repeats. It also contains a nuclear export signal, nuclear localization signal, and a cyclin-binding RXL motif. Localization of this protein to the nucleus has been shown experimentally, and interactions between this protein and cyclin-dependent kinase 2 have been observed. It has been suggested that this protein plays a role in both DNA replication and in both anti-viral and anti-bacterial innate immune pathways. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":73073376,"end":73258798,"strand":-1,"description":"ankyrin repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:23575]"}, {"versioned_ensembl_gene_id":"ENSG00000224388.1","gene_symbol":"BACE2-IT1","gene_name":"BACE2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:16024]","synonyms":"PRED43,NCRNA00228,C21orf75","biotype":"antisense_RNA","ncbi_id":"282569","summary":null,"start":41180097,"end":41180626,"strand":1,"description":"BACE2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:16024]"}, {"versioned_ensembl_gene_id":"ENSG00000237872.4","gene_symbol":"POU5F1P4","gene_name":"POU class 5 homeobox 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33310]","synonyms":"POU5FLC1,Oct4-pg4","biotype":"processed_pseudogene","ncbi_id":"645682","summary":null,"start":155433178,"end":155434262,"strand":1,"description":"POU class 5 homeobox 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33310]"}, {"versioned_ensembl_gene_id":"ENSG00000249888.1","gene_symbol":"AC106800.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43225506,"end":43225813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247763.2","gene_symbol":"AC106800.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43231812,"end":43233173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224414.1","gene_symbol":"AC010886.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":217693895,"end":217696763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254376.2","gene_symbol":"SOX5P1","gene_name":"SRY-box 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11202]","synonyms":"SOX5P,SOX29","biotype":"processed_pseudogene","ncbi_id":"6661","summary":null,"start":87788562,"end":87789688,"strand":-1,"description":"SRY-box 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11202]"}, {"versioned_ensembl_gene_id":"ENSG00000263788.1","gene_symbol":"AC061975.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28256375,"end":28256669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227382.1","gene_symbol":"EIF4A2P2","gene_name":"eukaryotic translation initiation factor 4A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421579","summary":null,"start":73199826,"end":73201225,"strand":1,"description":"eukaryotic translation initiation factor 4A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45099]"}, {"versioned_ensembl_gene_id":"ENSG00000216895.9","gene_symbol":"AC009403.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155611231,"end":155645205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185053.13","gene_symbol":"SGCZ","gene_name":"sarcoglycan zeta [Source:HGNC Symbol;Acc:HGNC:14075]","synonyms":"ZSG1","biotype":"protein_coding","ncbi_id":"137868","summary":"The zeta-sarcoglycan gene measures over 465 kb and localizes to 8p22. This protein is part of the sarcoglycan complex, a group of 6 proteins. The sarcoglycans are all N-glycosylated transmembrane proteins with a short intra-cellular domain, a single transmembrane region and a large extra-cellular domain containing a carboxyl-terminal cluster with several conserved cysteine residues. The sarcoglycan complex is part of the dystrophin-associated glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extra-cellular matrix. [provided by RefSeq, Jul 2008]","start":14089864,"end":15238339,"strand":-1,"description":"sarcoglycan zeta [Source:HGNC Symbol;Acc:HGNC:14075]"}, {"versioned_ensembl_gene_id":"ENSG00000236205.1","gene_symbol":"AL023773.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":142147862,"end":142148866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254145.1","gene_symbol":"AC134698.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43539137,"end":43539472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006194.9","gene_symbol":"ZNF263","gene_name":"zinc finger protein 263 [Source:HGNC Symbol;Acc:HGNC:13056]","synonyms":"ZSCAN44,ZKSCAN12,FPM315","biotype":"protein_coding","ncbi_id":"10127","summary":null,"start":3263800,"end":3301401,"strand":1,"description":"zinc finger protein 263 [Source:HGNC Symbol;Acc:HGNC:13056]"}, {"versioned_ensembl_gene_id":"ENSG00000189369.8","gene_symbol":"GSPT2","gene_name":"G1 to S phase transition 2 [Source:HGNC Symbol;Acc:HGNC:4622]","synonyms":"FLJ10441,eRF3b","biotype":"protein_coding","ncbi_id":"23708","summary":"This gene encodes a GTPase that belongs to the GTP-binding elongation factor family. The encoded protein is a polypeptide release factor that complexes with eukaryotic peptide chain release factor 1 to mediate translation termination. This protein may also be involved in mRNA stability.[provided by RefSeq, Mar 2010]","start":51743431,"end":51746232,"strand":1,"description":"G1 to S phase transition 2 [Source:HGNC Symbol;Acc:HGNC:4622]"}, {"versioned_ensembl_gene_id":"ENSG00000228158.2","gene_symbol":"TLE1P1","gene_name":"transducin like enhancer of split 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39438]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645381","summary":null,"start":65408084,"end":65408672,"strand":1,"description":"transducin like enhancer of split 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39438]"}, {"versioned_ensembl_gene_id":"ENSG00000283809.1","gene_symbol":"AC007326.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18906238,"end":18947732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244563.1","gene_symbol":"AC006011.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127846736,"end":127847084,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181074.4","gene_symbol":"OR52N4","gene_name":"olfactory receptor family 52 subfamily N member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15230]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390072","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5754243,"end":5755905,"strand":1,"description":"olfactory receptor family 52 subfamily N member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15230]"}, {"versioned_ensembl_gene_id":"ENSG00000131969.14","gene_symbol":"ABHD12B","gene_name":"abhydrolase domain containing 12B [Source:HGNC Symbol;Acc:HGNC:19837]","synonyms":"C14orf29,BEM46L3","biotype":"protein_coding","ncbi_id":"145447","summary":null,"start":50872160,"end":50904970,"strand":1,"description":"abhydrolase domain containing 12B [Source:HGNC Symbol;Acc:HGNC:19837]"}, {"versioned_ensembl_gene_id":"ENSG00000258687.1","gene_symbol":"AL358334.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50848122,"end":50865659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284602.1","gene_symbol":"AL031432.4","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":25232586,"end":25234775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000038358.14","gene_symbol":"EDC4","gene_name":"enhancer of mRNA decapping 4 [Source:HGNC Symbol;Acc:HGNC:17157]","synonyms":"RCD-8,HEDLS,Ge-1","biotype":"protein_coding","ncbi_id":"23644","summary":null,"start":67873023,"end":67884503,"strand":1,"description":"enhancer of mRNA decapping 4 [Source:HGNC Symbol;Acc:HGNC:17157]"}, {"versioned_ensembl_gene_id":"ENSG00000214960.9","gene_symbol":"ISPD","gene_name":"isoprenoid synthase domain containing [Source:HGNC Symbol;Acc:HGNC:37276]","synonyms":"Nip,IspD,hCG_1745121","biotype":"protein_coding","ncbi_id":"729920","summary":"This gene encodes a 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein. Mutations in this gene are the cause of Walker-Warburg syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":16087527,"end":16421322,"strand":-1,"description":"isoprenoid synthase domain containing [Source:HGNC Symbol;Acc:HGNC:37276]"}, {"versioned_ensembl_gene_id":"ENSG00000256984.2","gene_symbol":"AC008013.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":31012503,"end":31015806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234009.1","gene_symbol":"RPL5P34","gene_name":"ribosomal protein L5 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36463]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388907","summary":null,"start":42776406,"end":42777296,"strand":-1,"description":"ribosomal protein L5 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36463]"}, {"versioned_ensembl_gene_id":"ENSG00000279522.1","gene_symbol":"AC008536.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":112894933,"end":112896531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186310.9","gene_symbol":"NAP1L3","gene_name":"nucleosome assembly protein 1 like 3 [Source:HGNC Symbol;Acc:HGNC:7639]","synonyms":"NPL3,MGC26312,MB20","biotype":"protein_coding","ncbi_id":"4675","summary":"This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010]","start":93670930,"end":93673568,"strand":-1,"description":"nucleosome assembly protein 1 like 3 [Source:HGNC Symbol;Acc:HGNC:7639]"}, {"versioned_ensembl_gene_id":"ENSG00000272869.5","gene_symbol":"AC008575.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":112861188,"end":112893079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259584.1","gene_symbol":"AC021755.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40075204,"end":40078704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259527.2","gene_symbol":"LINC00052","gene_name":"long intergenic non-protein coding RNA 52 [Source:HGNC Symbol;Acc:HGNC:26455]","synonyms":"TMEM83,NCRNA00052,FLJ31461","biotype":"lincRNA","ncbi_id":"145978","summary":null,"start":87576929,"end":87579866,"strand":1,"description":"long intergenic non-protein coding RNA 52 [Source:HGNC Symbol;Acc:HGNC:26455]"}, {"versioned_ensembl_gene_id":"ENSG00000259414.1","gene_symbol":"AC242376.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23289303,"end":23293667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229127.1","gene_symbol":"AC007038.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":210030733,"end":210064356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198189.10","gene_symbol":"HSD17B11","gene_name":"hydroxysteroid 17-beta dehydrogenase 11 [Source:HGNC Symbol;Acc:HGNC:22960]","synonyms":"RetSDR2,PAN1B,DHRS8,17-BETA-HSDXI,17-BETA-HSD11,SDR16C2","biotype":"protein_coding","ncbi_id":"51170","summary":"Short-chain alcohol dehydrogenases, such as HSD17B11, metabolize secondary alcohols and ketones (Brereton et al., 2001 [PubMed 11165019]).[supplied by OMIM, Jun 2009]","start":87336610,"end":87391386,"strand":-1,"description":"hydroxysteroid 17-beta dehydrogenase 11 [Source:HGNC Symbol;Acc:HGNC:22960]"}, {"versioned_ensembl_gene_id":"ENSG00000230044.1","gene_symbol":"AC110754.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11665369,"end":11665969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169006.6","gene_symbol":"NTSR2","gene_name":"neurotensin receptor 2 [Source:HGNC Symbol;Acc:HGNC:8040]","synonyms":"NTR2","biotype":"protein_coding","ncbi_id":"23620","summary":"The protein encoded by this gene belongs to the G protein-coupled receptor family that activate a phosphatidylinositol-calcium second messenger system. Binding and pharmacological studies demonstrate that this receptor binds neurotensin as well as several other ligands already described for neurotensin NT1 receptor. However, unlike NT1 receptor, this gene recognizes, with high affinity, levocabastine, a histamine H1 receptor antagonist previously shown to compete with neurotensin for low-affinity binding sites in brain. These activities suggest that this receptor may be of physiological importance and that a natural agonist for the receptor may exist. [provided by RefSeq, Jul 2008]","start":11658178,"end":11670164,"strand":-1,"description":"neurotensin receptor 2 [Source:HGNC Symbol;Acc:HGNC:8040]"}, {"versioned_ensembl_gene_id":"ENSG00000279447.1","gene_symbol":"AL118508.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23071547,"end":23072722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239648.1","gene_symbol":"MTND1P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288984","summary":null,"start":141803701,"end":141804652,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42052]"}, {"versioned_ensembl_gene_id":"ENSG00000257611.1","gene_symbol":"AC010182.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106170004,"end":106172437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231948.2","gene_symbol":"HS1BP3-IT1","gene_name":"HS1BP3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41474]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874343","summary":null,"start":20590775,"end":20592548,"strand":-1,"description":"HS1BP3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41474]"}, {"versioned_ensembl_gene_id":"ENSG00000270141.3","gene_symbol":"TERC","gene_name":"telomerase RNA component [Source:HGNC Symbol;Acc:HGNC:11727]","synonyms":"TRC3,TR,SCARNA19,hTR","biotype":"lincRNA","ncbi_id":"7012","summary":"Telomerase is a ribonucleoprotein polymerase that maintains telomere ends by addition of the telomere repeat TTAGGG. The enzyme consists of a protein component with reverse transcriptase activity, and an RNA component, encoded by this gene, that serves as a template for the telomere repeat. Telomerase expression plays a role in cellular senescence, as it is normally repressed in postnatal somatic cells resulting in progressive shortening of telomeres. Deregulation of telomerase expression in somatic cells may be involved in oncogenesis. Studies in mouse suggest that telomerase also participates in chromosomal repair, since de novo synthesis of telomere repeats may occur at double-stranded breaks. Mutations in this gene cause autosomal dominant dyskeratosis congenita, and may also be associated with some cases of aplastic anemia. [provided by RefSeq, Jul 2008]","start":169764520,"end":169765060,"strand":-1,"description":"telomerase RNA component [Source:HGNC Symbol;Acc:HGNC:11727]"}, {"versioned_ensembl_gene_id":"ENSG00000230796.1","gene_symbol":"AC064862.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57650381,"end":57651119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237545.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"AB023060.6,POLR2LP","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31133166,"end":31133352,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000274538.2","gene_symbol":"PHLDA2","gene_name":"pleckstrin homology like domain family A member 2 [Source:HGNC Symbol;Acc:HGNC:12385]","synonyms":"IPL,HLDA2,BWR1C,TSSC3","biotype":"protein_coding","ncbi_id":"7262","summary":"This gene is located in a cluster of imprinted genes on chromosome 11p15.5, which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene has been shown to be imprinted, with preferential expression from the maternal allele in placenta and liver. [provided by RefSeq, Oct 2010]","start":2928201,"end":2929383,"strand":-1,"description":"pleckstrin homology like domain family A member 2 [Source:HGNC Symbol;Acc:HGNC:12385]"}, {"versioned_ensembl_gene_id":"ENSG00000242335.8","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31938304,"end":31944738,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000127957.17","gene_symbol":"PMS2P3","gene_name":"PMS1 homolog 2, mismatch repair system component pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9128]","synonyms":"PMSR3,PMS5,PMS2L9,PMS2L3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5387","summary":null,"start":75502930,"end":75528148,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9128]"}, {"versioned_ensembl_gene_id":"ENSG00000078403.16","gene_symbol":"MLLT10","gene_name":"MLLT10, histone lysine methyltransferase DOT1L cofactor [Source:HGNC Symbol;Acc:HGNC:16063]","synonyms":"AF10","biotype":"protein_coding","ncbi_id":"8028","summary":"This gene encodes a transcription factor and has been identified as a partner gene involved in several chromosomal rearrangements resulting in various leukemias. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]","start":21524675,"end":21743630,"strand":1,"description":"MLLT10, histone lysine methyltransferase DOT1L cofactor [Source:HGNC Symbol;Acc:HGNC:16063]"}, {"versioned_ensembl_gene_id":"ENSG00000274517.1","gene_symbol":"AC098784.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54712477,"end":54712760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227182.1","gene_symbol":"VN1R28P","gene_name":"vomeronasal 1 receptor 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:37348]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100312785","summary":null,"start":57422830,"end":57423725,"strand":-1,"description":"vomeronasal 1 receptor 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:37348]"}, {"versioned_ensembl_gene_id":"ENSG00000230583.6","gene_symbol":"GTF2IRD1P1","gene_name":"GTF2I repeat domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44136]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729156","summary":null,"start":66809993,"end":66844826,"strand":-1,"description":"GTF2I repeat domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44136]"}, {"versioned_ensembl_gene_id":"ENSG00000204365.5","gene_symbol":"C10orf126","gene_name":"chromosome 10 open reading frame 126 [Source:HGNC Symbol;Acc:HGNC:28693]","synonyms":"bA492M23.1,MGC45541","biotype":"protein_coding","ncbi_id":"283080","summary":null,"start":28846408,"end":28881898,"strand":1,"description":"chromosome 10 open reading frame 126 [Source:HGNC Symbol;Acc:HGNC:28693]"}, {"versioned_ensembl_gene_id":"ENSG00000239467.5","gene_symbol":"AC007405.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170771113,"end":170778148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197901.11","gene_symbol":"SLC22A6","gene_name":"solute carrier family 22 member 6 [Source:HGNC Symbol;Acc:HGNC:10970]","synonyms":"ROAT1,PAHT,OAT1","biotype":"protein_coding","ncbi_id":"9356","summary":"The protein encoded by this gene is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":62936385,"end":62984983,"strand":-1,"description":"solute carrier family 22 member 6 [Source:HGNC Symbol;Acc:HGNC:10970]"}, {"versioned_ensembl_gene_id":"ENSG00000226262.1","gene_symbol":"PHKBP1","gene_name":"phosphorylase kinase regulatory subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5258","summary":null,"start":8097824,"end":8099774,"strand":-1,"description":"phosphorylase kinase regulatory subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8928]"}, {"versioned_ensembl_gene_id":"ENSG00000237225.1","gene_symbol":"OR13K1P","gene_name":"olfactory receptor family 13 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14721]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402424","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131562738,"end":131563834,"strand":1,"description":"olfactory receptor family 13 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14721]"}, {"versioned_ensembl_gene_id":"ENSG00000197713.14","gene_symbol":"RPE","gene_name":"ribulose-5-phosphate-3-epimerase [Source:HGNC Symbol;Acc:HGNC:10293]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6120","summary":null,"start":210002565,"end":210022259,"strand":1,"description":"ribulose-5-phosphate-3-epimerase [Source:HGNC Symbol;Acc:HGNC:10293]"}, {"versioned_ensembl_gene_id":"ENSG00000121851.12","gene_symbol":"POLR3GL","gene_name":"RNA polymerase III subunit G like [Source:HGNC Symbol;Acc:HGNC:28466]","synonyms":"MGC3200,flj32422","biotype":"protein_coding","ncbi_id":"84265","summary":null,"start":145964702,"end":145978848,"strand":1,"description":"RNA polymerase III subunit G like [Source:HGNC Symbol;Acc:HGNC:28466]"}, {"versioned_ensembl_gene_id":"ENSG00000240882.1","gene_symbol":"AC063952.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120306726,"end":120307952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260908.1","gene_symbol":"AC009093.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29053732,"end":29108108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172508.10","gene_symbol":"CARNS1","gene_name":"carnosine synthase 1 [Source:HGNC Symbol;Acc:HGNC:29268]","synonyms":"KIAA1394,ATPGD1","biotype":"protein_coding","ncbi_id":"57571","summary":"CARNS1 (EC 6.3.2.11), a member of the ATP-grasp family of ATPases, catalyzes the formation of carnosine (beta-alanyl-L-histidine) and homocarnosine (gamma-aminobutyryl-L-histidine), which are found mainly in skeletal muscle and the central nervous system, respectively (Drozak et al., 2010 [PubMed 20097752]).[supplied by OMIM, Apr 2010]","start":67414968,"end":67425607,"strand":1,"description":"carnosine synthase 1 [Source:HGNC Symbol;Acc:HGNC:29268]"}, {"versioned_ensembl_gene_id":"ENSG00000270678.1","gene_symbol":"AL670379.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120932901,"end":120933152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078124.11","gene_symbol":"ACER3","gene_name":"alkaline ceramidase 3 [Source:HGNC Symbol;Acc:HGNC:16066]","synonyms":"PHCA,FLJ11238,APHC","biotype":"protein_coding","ncbi_id":"55331","summary":null,"start":76860867,"end":77026797,"strand":1,"description":"alkaline ceramidase 3 [Source:HGNC Symbol;Acc:HGNC:16066]"}, {"versioned_ensembl_gene_id":"ENSG00000277862.1","gene_symbol":"PRAMEF34P","gene_name":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"649324","summary":null,"start":13095179,"end":13097971,"strand":-1,"description":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]"}, {"versioned_ensembl_gene_id":"ENSG00000254988.1","gene_symbol":"AP002498.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76955417,"end":76978619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224341.1","gene_symbol":"AC006965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118877886,"end":118879185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175482.8","gene_symbol":"POLD4","gene_name":"DNA polymerase delta 4, accessory subunit [Source:HGNC Symbol;Acc:HGNC:14106]","synonyms":"POLDS,p12","biotype":"protein_coding","ncbi_id":"57804","summary":"This gene encodes the smallest subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. The encoded protein enhances the activity of DNA polymerase delta and plays a role in fork repair and stabilization through interactions with the DNA helicase Bloom syndrome protein. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":67350777,"end":67356972,"strand":-1,"description":"DNA polymerase delta 4, accessory subunit [Source:HGNC Symbol;Acc:HGNC:14106]"}, {"versioned_ensembl_gene_id":"ENSG00000275484.1","gene_symbol":"AP003419.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67374416,"end":67374932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278317.1","gene_symbol":"AC011890.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120709061,"end":120709392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277058.2","gene_symbol":"HNRNPCL3","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"649330","summary":null,"start":13060869,"end":13062229,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]"}, {"versioned_ensembl_gene_id":"ENSG00000213938.3","gene_symbol":"SEPHS1P6","gene_name":"selenophosphate synthetase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42168]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729399","summary":null,"start":199659551,"end":199660729,"strand":1,"description":"selenophosphate synthetase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42168]"}, {"versioned_ensembl_gene_id":"ENSG00000237861.1","gene_symbol":"AL513325.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197222222,"end":197223255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273899.4","gene_symbol":"NOL12","gene_name":"nucleolar protein 12 [Source:HGNC Symbol;Acc:HGNC:28585]","synonyms":"RRP17,Nop25,MGC3731","biotype":"protein_coding","ncbi_id":"79159","summary":null,"start":37681673,"end":37693478,"strand":1,"description":"nucleolar protein 12 [Source:HGNC Symbol;Acc:HGNC:28585]"}, {"versioned_ensembl_gene_id":"ENSG00000274575.2","gene_symbol":"IGLV1-40","gene_name":"immunoglobulin lambda variable 1-40 [Source:HGNC Symbol;Acc:HGNC:5877]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28825","summary":null,"start":22418863,"end":22419379,"strand":1,"description":"immunoglobulin lambda variable 1-40 [Source:HGNC Symbol;Acc:HGNC:5877]"}, {"versioned_ensembl_gene_id":"ENSG00000281565.1","gene_symbol":"IGLV1-41","gene_name":"immunoglobulin lambda variable 1-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5878]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28824","summary":null,"start":22413303,"end":22413817,"strand":1,"description":"immunoglobulin lambda variable 1-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5878]"}, {"versioned_ensembl_gene_id":"ENSG00000237371.1","gene_symbol":"AL355803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64056803,"end":64057084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267448.5","gene_symbol":"AC010649.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3296765,"end":3303003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259432.1","gene_symbol":"AC023908.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39813223,"end":39815429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240032.1","gene_symbol":"LNCSRLR","gene_name":"lncRNA sorafenib resistance in renal cell carcinoma associated [Source:HGNC Symbol;Acc:HGNC:52753]","synonyms":"lncRNA-SRLR","biotype":"antisense_RNA","ncbi_id":"109729161","summary":null,"start":146066344,"end":146069185,"strand":-1,"description":"lncRNA sorafenib resistance in renal cell carcinoma associated [Source:HGNC Symbol;Acc:HGNC:52753]"}, {"versioned_ensembl_gene_id":"ENSG00000226180.3","gene_symbol":"AC010536.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87693537,"end":87696147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275984.1","gene_symbol":"AC011515.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54679429,"end":54680789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248145.1","gene_symbol":"AC016553.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13175846,"end":13179572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130158.13","gene_symbol":"DOCK6","gene_name":"dedicator of cytokinesis 6 [Source:HGNC Symbol;Acc:HGNC:19189]","synonyms":"ZIR1,KIAA1395","biotype":"protein_coding","ncbi_id":"57572","summary":"This gene encodes a member of the dedicator of cytokinesis (DOCK) family of atypical guanine nucleotide exchange factors. Guanine nucleotide exchange factors interact with small GTPases and are components of intracellular signaling networks. The encoded protein is a group C DOCK protein and plays a role in actin cytoskeletal reorganization by activating the Rho GTPases Cdc42 and Rac1. Mutations in this gene are associated with Adams-Oliver syndrome 2. [provided by RefSeq, Dec 2011]","start":11199295,"end":11262481,"strand":-1,"description":"dedicator of cytokinesis 6 [Source:HGNC Symbol;Acc:HGNC:19189]"}, {"versioned_ensembl_gene_id":"ENSG00000273733.1","gene_symbol":"AC011472.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11221083,"end":11221573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248196.1","gene_symbol":"AC092658.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87166844,"end":87167734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225573.4","gene_symbol":"RPL35P5","gene_name":"ribosomal protein L35 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36955]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441246","summary":null,"start":66606738,"end":66607107,"strand":-1,"description":"ribosomal protein L35 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36955]"}, {"versioned_ensembl_gene_id":"ENSG00000236353.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"HOX12,G17,PBX2MHC","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32261167,"end":32266609,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000100949.14","gene_symbol":"RABGGTA","gene_name":"Rab geranylgeranyltransferase alpha subunit [Source:HGNC Symbol;Acc:HGNC:9795]","synonyms":"PTAR3","biotype":"protein_coding","ncbi_id":"5875","summary":null,"start":24265538,"end":24271739,"strand":-1,"description":"Rab geranylgeranyltransferase alpha subunit [Source:HGNC Symbol;Acc:HGNC:9795]"}, {"versioned_ensembl_gene_id":"ENSG00000233140.6","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAPSAR1,TAP1-AS1,XXbac-BPG246D15.8","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32934803,"end":32937212,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000122872.8","gene_symbol":"ARL4AP1","gene_name":"ADP ribosylation factor like GTPase 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17741]","synonyms":"Em:AC022390.2,ARL4P,ARL4B","biotype":"processed_pseudogene","ncbi_id":"387684","summary":null,"start":60684505,"end":60685209,"strand":1,"description":"ADP ribosylation factor like GTPase 4A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17741]"}, {"versioned_ensembl_gene_id":"ENSG00000238034.1","gene_symbol":"AL109807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21947647,"end":21970783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173320.11","gene_symbol":"STOX2","gene_name":"storkhead box 2 [Source:HGNC Symbol;Acc:HGNC:25450]","synonyms":"DKFZp762K222","biotype":"protein_coding","ncbi_id":"56977","summary":"This gene encodes a Storkhead-box_winged-helix domain containing protein. This protein is differentially expressed in decidual tissue and may be involved in the susceptibility to pre-eclampsia with fetal growth restriction. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":183797692,"end":184023526,"strand":1,"description":"storkhead box 2 [Source:HGNC Symbol;Acc:HGNC:25450]"}, {"versioned_ensembl_gene_id":"ENSG00000272703.1","gene_symbol":"AP005137.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11857155,"end":11857554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282073.1","gene_symbol":"AC243660.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28540731,"end":28540883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138134.11","gene_symbol":"STAMBPL1","gene_name":"STAM binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:24105]","synonyms":"ALMalpha,KIAA1373,FLJ31524,bA399O19.2,AMSH-LP,AMSH-FP","biotype":"protein_coding","ncbi_id":"57559","summary":null,"start":88879734,"end":88975153,"strand":1,"description":"STAM binding protein like 1 [Source:HGNC Symbol;Acc:HGNC:24105]"}, {"versioned_ensembl_gene_id":"ENSG00000265316.1","gene_symbol":"AP005059.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5463627,"end":5480975,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033100.16","gene_symbol":"CHPF2","gene_name":"chondroitin polymerizing factor 2 [Source:HGNC Symbol;Acc:HGNC:29270]","synonyms":"KIAA1402,CSGlcA-T,ChSy-3","biotype":"protein_coding","ncbi_id":"54480","summary":null,"start":151232489,"end":151238827,"strand":1,"description":"chondroitin polymerizing factor 2 [Source:HGNC Symbol;Acc:HGNC:29270]"}, {"versioned_ensembl_gene_id":"ENSG00000241684.5","gene_symbol":"ADAMTS9-AS2","gene_name":"ADAMTS9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42435]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507098","summary":null,"start":64684909,"end":65011468,"strand":1,"description":"ADAMTS9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42435]"}, {"versioned_ensembl_gene_id":"ENSG00000177418.2","gene_symbol":"AC006001.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66556889,"end":66557362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229180.6","gene_symbol":"AC006001.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66526088,"end":66592397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267433.1","gene_symbol":"AC008798.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29901696,"end":29901869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261324.2","gene_symbol":"AC010168.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":14762504,"end":14767931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055917.15","gene_symbol":"PUM2","gene_name":"pumilio RNA binding family member 2 [Source:HGNC Symbol;Acc:HGNC:14958]","synonyms":"KIAA0235,PUMH2","biotype":"protein_coding","ncbi_id":"23369","summary":"This gene encodes a protein that belongs to a family of RNA-binding proteins. The encoded protein functions as a translational repressor during embryonic development and cell differentiation. This protein is also thought to be a positive regulator of cell proliferation in adipose-derived stem cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":20248691,"end":20352234,"strand":-1,"description":"pumilio RNA binding family member 2 [Source:HGNC Symbol;Acc:HGNC:14958]"}, {"versioned_ensembl_gene_id":"ENSG00000206232.8","gene_symbol":"PSMB8-AS1","gene_name":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]","synonyms":"TAPSAR1,TAP1-AS1,XXbac-BPG246D15.8","biotype":"processed_transcript","ncbi_id":"100507463","summary":null,"start":32822063,"end":32824472,"strand":1,"description":"PSMB8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:39758]"}, {"versioned_ensembl_gene_id":"ENSG00000171135.13","gene_symbol":"JAGN1","gene_name":"jagunal homolog 1 [Source:HGNC Symbol;Acc:HGNC:26926]","synonyms":"GL009,FLJ14602","biotype":"protein_coding","ncbi_id":"84522","summary":"The protein encoded by this gene is a transmembrane protein. It functions in the early secretory pathway and is necessary for neutrophil differentiation and survival. Mutations in this gene result in severe congenital neutropenia. [provided by RefSeq, Oct 2014]","start":9890554,"end":9894349,"strand":1,"description":"jagunal homolog 1 [Source:HGNC Symbol;Acc:HGNC:26926]"}, {"versioned_ensembl_gene_id":"ENSG00000128536.15","gene_symbol":"CDHR3","gene_name":"cadherin related family member 3 [Source:HGNC Symbol;Acc:HGNC:26308]","synonyms":"FLJ44366,FLJ23834,CDH28","biotype":"protein_coding","ncbi_id":"222256","summary":null,"start":105876796,"end":106033773,"strand":1,"description":"cadherin related family member 3 [Source:HGNC Symbol;Acc:HGNC:26308]"}, {"versioned_ensembl_gene_id":"ENSG00000267122.1","gene_symbol":"AC004490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2212029,"end":2215565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104885.17","gene_symbol":"DOT1L","gene_name":"DOT1 like histone lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:24948]","synonyms":"KMT4,KIAA1814,DOT1","biotype":"protein_coding","ncbi_id":"84444","summary":"The protein encoded by this gene is a histone methyltransferase that methylates lysine-79 of histone H3. It is inactive against free core histones, but shows significant histone methyltransferase activity against nucleosomes. [provided by RefSeq, Aug 2011]","start":2164149,"end":2232578,"strand":1,"description":"DOT1 like histone lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:24948]"}, {"versioned_ensembl_gene_id":"ENSG00000161944.16","gene_symbol":"ASGR2","gene_name":"asialoglycoprotein receptor 2 [Source:HGNC Symbol;Acc:HGNC:743]","synonyms":"CLEC4H2","biotype":"protein_coding","ncbi_id":"433","summary":"This gene encodes a subunit of the asialoglycoprotein receptor. This receptor is a transmembrane protein that plays a critical role in serum glycoprotein homeostasis by mediating the endocytosis and lysosomal degradation of glycoproteins with exposed terminal galactose or N-acetylgalactosamine residues. The asialoglycoprotein receptor may facilitate hepatic infection by multiple viruses including hepatitis B, and is also a target for liver-specific drug delivery. The asialoglycoprotein receptor is a hetero-oligomeric protein composed of major and minor subunits, which are encoded by different genes. The protein encoded by this gene is the less abundant minor subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":7101322,"end":7115700,"strand":-1,"description":"asialoglycoprotein receptor 2 [Source:HGNC Symbol;Acc:HGNC:743]"}, {"versioned_ensembl_gene_id":"ENSG00000254197.1","gene_symbol":"AC011676.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141278228,"end":141292862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213411.2","gene_symbol":"RBM22P2","gene_name":"RNA binding motif protein 22 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271871","summary":null,"start":30539597,"end":30543461,"strand":-1,"description":"RNA binding motif protein 22 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39695]"}, {"versioned_ensembl_gene_id":"ENSG00000232489.1","gene_symbol":"MFAP1P1","gene_name":"microfibril associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39694]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646755","summary":null,"start":30541643,"end":30542897,"strand":-1,"description":"microfibril associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39694]"}, {"versioned_ensembl_gene_id":"ENSG00000169906.5","gene_symbol":"S100G","gene_name":"S100 calcium binding protein G [Source:HGNC Symbol;Acc:HGNC:1436]","synonyms":"CALB3,CABP9K,CABP1","biotype":"protein_coding","ncbi_id":"795","summary":"This gene encodes calbindin D9K, a vitamin D-dependent calcium-binding protein. This cytosolic protein belongs to a family of calcium-binding proteins that includes calmodulin, parvalbumin, troponin C, and S100 protein. In the intestine, the protein is vitamin D-dependent and its expression correlates with calcium transport activity. The protein may increase Ca2+ absorption by buffering Ca2+ in the cytoplasm and increase ATP-dependent Ca2+ transport in duodenal basolateral membrane vesicles. [provided by RefSeq, Jul 2008]","start":16650158,"end":16654670,"strand":1,"description":"S100 calcium binding protein G [Source:HGNC Symbol;Acc:HGNC:1436]"}, {"versioned_ensembl_gene_id":"ENSG00000112699.10","gene_symbol":"GMDS","gene_name":"GDP-mannose 4,6-dehydratase [Source:HGNC Symbol;Acc:HGNC:4369]","synonyms":"SDR3E1,GMD","biotype":"protein_coding","ncbi_id":"2762","summary":"GDP-mannose 4,6-dehydratase (GMD; EC 4.2.1.47) catalyzes the conversion of GDP-mannose to GDP-4-keto-6-deoxymannose, the first step in the synthesis of GDP-fucose from GDP-mannose, using NADP+ as a cofactor. The second and third steps of the pathway are catalyzed by a single enzyme, GDP-keto-6-deoxymannose 3,5-epimerase, 4-reductase, designated FX in humans (MIM 137020).[supplied by OMIM, Aug 2009]","start":1623806,"end":2245692,"strand":-1,"description":"GDP-mannose 4,6-dehydratase [Source:HGNC Symbol;Acc:HGNC:4369]"}, {"versioned_ensembl_gene_id":"ENSG00000105650.21","gene_symbol":"PDE4C","gene_name":"phosphodiesterase 4C [Source:HGNC Symbol;Acc:HGNC:8782]","synonyms":"DPDE1","biotype":"protein_coding","ncbi_id":"5143","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE4 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":18207961,"end":18255419,"strand":-1,"description":"phosphodiesterase 4C [Source:HGNC Symbol;Acc:HGNC:8782]"}, {"versioned_ensembl_gene_id":"ENSG00000275921.5","gene_symbol":"CU633846.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54867554,"end":54882047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259209.3","gene_symbol":"AC004943.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72805998,"end":72809872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125813.13","gene_symbol":"PAX1","gene_name":"paired box 1 [Source:HGNC Symbol;Acc:HGNC:8615]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5075","summary":"This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. This gene plays a role in pattern formation during embryogenesis and may be essential for development of the vertebral column. This gene is silenced by methylation in ovarian and cervical cancers and may be a tumor suppressor gene. Mutations in this gene are also associated with vertebral malformations. [provided by RefSeq, Mar 2012]","start":21705659,"end":21718486,"strand":1,"description":"paired box 1 [Source:HGNC Symbol;Acc:HGNC:8615]"}, {"versioned_ensembl_gene_id":"ENSG00000101445.9","gene_symbol":"PPP1R16B","gene_name":"protein phosphatase 1 regulatory subunit 16B [Source:HGNC Symbol;Acc:HGNC:15850]","synonyms":"TIMAP,KIAA0823,ANKRD4","biotype":"protein_coding","ncbi_id":"26051","summary":"The protein encoded by this gene is membrane-associated and contains five ankyrin repeats, a protein phosphatase-1-interacting domain, and a carboxy-terminal CAAX box domain. Synthesis of the encoded protein is inhibited by transforming growth factor beta-1. The protein may bind to the membrane through its CAAX box domain and may act as a signaling molecule through interaction with protein phosphatase-1. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]","start":38805705,"end":38923024,"strand":1,"description":"protein phosphatase 1 regulatory subunit 16B [Source:HGNC Symbol;Acc:HGNC:15850]"}, {"versioned_ensembl_gene_id":"ENSG00000259940.2","gene_symbol":"AC109449.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27213308,"end":27214993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205143.2","gene_symbol":"ARID3C","gene_name":"AT-rich interaction domain 3C [Source:HGNC Symbol;Acc:HGNC:21209]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138715","summary":"This gene is a member of the ARID (AT-rich interaction domain) family of proteins. The ARID domain is a helix-turn-helix motif-based DNA-binding domain. ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]","start":34621379,"end":34628107,"strand":-1,"description":"AT-rich interaction domain 3C [Source:HGNC Symbol;Acc:HGNC:21209]"}, {"versioned_ensembl_gene_id":"ENSG00000224844.1","gene_symbol":"AC107079.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":237122910,"end":237124097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082996.19","gene_symbol":"RNF13","gene_name":"ring finger protein 13 [Source:HGNC Symbol;Acc:HGNC:10057]","synonyms":"RZF","biotype":"protein_coding","ncbi_id":"11342","summary":"The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008]","start":149812708,"end":149962139,"strand":1,"description":"ring finger protein 13 [Source:HGNC Symbol;Acc:HGNC:10057]"}, {"versioned_ensembl_gene_id":"ENSG00000163875.15","gene_symbol":"MEAF6","gene_name":"MYST/Esa1 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:25674]","synonyms":"NY-SAR-91,FLJ11730,Eaf6,CENP-28,C1orf149","biotype":"protein_coding","ncbi_id":"64769","summary":"This gene encodes a nuclear protein involved in transcriptional activation. The encoded protein may form a component of several different histone acetyltransferase complexes. There is a pseudogene for this gene on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":37492575,"end":37514774,"strand":-1,"description":"MYST/Esa1 associated factor 6 [Source:HGNC Symbol;Acc:HGNC:25674]"}, {"versioned_ensembl_gene_id":"ENSG00000261045.2","gene_symbol":"LINC02129","gene_name":"long intergenic non-protein coding RNA 2129 [Source:HGNC Symbol;Acc:HGNC:52988]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371156","summary":null,"start":27158451,"end":27176587,"strand":-1,"description":"long intergenic non-protein coding RNA 2129 [Source:HGNC Symbol;Acc:HGNC:52988]"}, {"versioned_ensembl_gene_id":"ENSG00000197256.10","gene_symbol":"KANK2","gene_name":"KN motif and ankyrin repeat domains 2 [Source:HGNC Symbol;Acc:HGNC:29300]","synonyms":"MXRA3,KIAA1518,ANKRD25","biotype":"protein_coding","ncbi_id":"25959","summary":"This gene encodes a member of the KN motif and ankyrin repeat domains (KANK) family of proteins, which play a role in cytoskeletal formation by regulating actin polymerization. The encoded protein functions in the sequestration of steroid receptor coactivators and possibly other proteins. Mutations in this gene are associated with impaired kidney podocyte function and nephrotic syndrome, and keratoderma and woolly hair. [provided by RefSeq, Jul 2016]","start":11164267,"end":11197791,"strand":-1,"description":"KN motif and ankyrin repeat domains 2 [Source:HGNC Symbol;Acc:HGNC:29300]"}, {"versioned_ensembl_gene_id":"ENSG00000187979.4","gene_symbol":"AC008079.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18178038,"end":18205915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284516.1","gene_symbol":"AC116631.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":82284971,"end":82340013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223856.1","gene_symbol":"RAB9AP2","gene_name":"RAB9A, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38106]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287542","summary":null,"start":25709908,"end":25713557,"strand":-1,"description":"RAB9A, member RAS oncogene family pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38106]"}, {"versioned_ensembl_gene_id":"ENSG00000119787.13","gene_symbol":"ATL2","gene_name":"atlastin GTPase 2 [Source:HGNC Symbol;Acc:HGNC:24047]","synonyms":"ARL6IP2","biotype":"protein_coding","ncbi_id":"64225","summary":null,"start":38294880,"end":38377285,"strand":-1,"description":"atlastin GTPase 2 [Source:HGNC Symbol;Acc:HGNC:24047]"}, {"versioned_ensembl_gene_id":"ENSG00000182389.19","gene_symbol":"CACNB4","gene_name":"calcium voltage-gated channel auxiliary subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:1404]","synonyms":"EJM4","biotype":"protein_coding","ncbi_id":"785","summary":"This gene encodes a member of the beta subunit family of voltage-dependent calcium channel complex proteins. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Various versions of each of these subunits exist, either expressed from similar genes or the result of alternative splicing. The protein encoded by this locus plays an important role in calcium channel function by modulating G protein inhibition, increasing peak calcium current, controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation. Certain mutations in this gene have been associated with idiopathic generalized epilepsy (IGE), juvenile myoclonic epilepsy (JME), and episodic ataxia, type 5. [provided by RefSeq, Aug 2016]","start":151832768,"end":152099475,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:1404]"}, {"versioned_ensembl_gene_id":"ENSG00000158022.6","gene_symbol":"TRIM63","gene_name":"tripartite motif containing 63 [Source:HGNC Symbol;Acc:HGNC:16007]","synonyms":"SMRZ,RNF28,MURF-1,IRF","biotype":"protein_coding","ncbi_id":"84676","summary":"This gene encodes a member of the RING zinc finger protein family found in striated muscle and iris. The product of this gene is an E3 ubiquitin ligase that localizes to the Z-line and M-line lattices of myofibrils. This protein plays an important role in the atrophy of skeletal and cardiac muscle and is required for the degradation of myosin heavy chain proteins, myosin light chain, myosin binding protein, and for muscle-type creatine kinase. [provided by RefSeq, Feb 2012]","start":26051304,"end":26068436,"strand":-1,"description":"tripartite motif containing 63 [Source:HGNC Symbol;Acc:HGNC:16007]"}, {"versioned_ensembl_gene_id":"ENSG00000232794.1","gene_symbol":"HNRNPDP1","gene_name":"heterogeneous nuclear ribonucleoprotein D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5038]","synonyms":"HNRPDP,HNRNPDP,AUF1P,AUF1B","biotype":"processed_pseudogene","ncbi_id":"8251","summary":null,"start":64044305,"end":64045058,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5038]"}, {"versioned_ensembl_gene_id":"ENSG00000131724.10","gene_symbol":"IL13RA1","gene_name":"interleukin 13 receptor subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:5974]","synonyms":"NR4,IL-13Ra,CD213a1","biotype":"protein_coding","ncbi_id":"3597","summary":"The protein encoded by this gene is a subunit of the interleukin 13 receptor. This subunit forms a receptor complex with IL4 receptor alpha, a subunit shared by IL13 and IL4 receptors. This subunit serves as a primary IL13-binding subunit of the IL13 receptor, and may also be a component of IL4 receptors. This protein has been shown to bind tyrosine kinase TYK2, and thus may mediate the signaling processes that lead to the activation of JAK1, STAT3 and STAT6 induced by IL13 and IL4. [provided by RefSeq, Jul 2008]","start":118727572,"end":118794539,"strand":1,"description":"interleukin 13 receptor subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:5974]"}, {"versioned_ensembl_gene_id":"ENSG00000237260.1","gene_symbol":"AC073069.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176338637,"end":176339077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248374.1","gene_symbol":"AC073358.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":143620528,"end":143627690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230757.1","gene_symbol":"NFU1P1","gene_name":"NFU1 iron-sulfur cluster scaffold pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132681","summary":null,"start":39643638,"end":39644705,"strand":1,"description":"NFU1 iron-sulfur cluster scaffold pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44553]"}, {"versioned_ensembl_gene_id":"ENSG00000227375.5","gene_symbol":"DLG1-AS1","gene_name":"DLG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44154]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507086","summary":null,"start":197298252,"end":197303747,"strand":1,"description":"DLG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44154]"}, {"versioned_ensembl_gene_id":"ENSG00000169903.6","gene_symbol":"TM4SF4","gene_name":"transmembrane 4 L six family member 4 [Source:HGNC Symbol;Acc:HGNC:11856]","synonyms":"il-TMP","biotype":"protein_coding","ncbi_id":"7104","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that can regulate cell proliferation.[provided by RefSeq, Mar 2011]","start":149473974,"end":149503281,"strand":1,"description":"transmembrane 4 L six family member 4 [Source:HGNC Symbol;Acc:HGNC:11856]"}, {"versioned_ensembl_gene_id":"ENSG00000228147.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31121049,"end":31126854,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000158859.9","gene_symbol":"ADAMTS4","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 4 [Source:HGNC Symbol;Acc:HGNC:220]","synonyms":"KIAA0688,ADMP-1,ADAMTS-2","biotype":"protein_coding","ncbi_id":"9507","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of this family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene lacks a C-terminal TS motif. The encoded preproprotein is proteolytically processed to generate the mature protease. This protease is responsible for the degradation of aggrecan, a major proteoglycan of cartilage, and brevican, a brain-specific extracellular matrix protein. The expression of this gene is upregulated in arthritic disease and this may contribute to disease progression through the degradation of aggrecan. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":161184308,"end":161199056,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 4 [Source:HGNC Symbol;Acc:HGNC:220]"}, {"versioned_ensembl_gene_id":"ENSG00000224485.1","gene_symbol":"USP9YP7","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38079]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100462821","summary":null,"start":17908755,"end":17910806,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38079]"}, {"versioned_ensembl_gene_id":"ENSG00000225642.1","gene_symbol":"SNRPEP5","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43447]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874413","summary":null,"start":8603082,"end":8603359,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43447]"}, {"versioned_ensembl_gene_id":"ENSG00000254618.1","gene_symbol":"TMED10P1","gene_name":"transmembrane p24 trafficking protein 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30754]","synonyms":"Tmp21-II,TMED10P","biotype":"processed_pseudogene","ncbi_id":"286102","summary":null,"start":144994886,"end":144995540,"strand":1,"description":"transmembrane p24 trafficking protein 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30754]"}, {"versioned_ensembl_gene_id":"ENSG00000253266.1","gene_symbol":"AC100860.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141055290,"end":141060596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196196.2","gene_symbol":"HRCT1","gene_name":"histidine rich carboxyl terminus 1 [Source:HGNC Symbol;Acc:HGNC:33872]","synonyms":"UNQ338,PRO537,LGLL338","biotype":"protein_coding","ncbi_id":"646962","summary":null,"start":35906192,"end":35907141,"strand":1,"description":"histidine rich carboxyl terminus 1 [Source:HGNC Symbol;Acc:HGNC:33872]"}, {"versioned_ensembl_gene_id":"ENSG00000230604.2","gene_symbol":"TSEN15P2","gene_name":"tRNA splicing endonuclease subunit 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43963]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480781","summary":null,"start":51859778,"end":51860135,"strand":1,"description":"tRNA splicing endonuclease subunit 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43963]"}, {"versioned_ensembl_gene_id":"ENSG00000236973.2","gene_symbol":"GAPDHP51","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:38557]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421271","summary":null,"start":51707138,"end":51708137,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:38557]"}, {"versioned_ensembl_gene_id":"ENSG00000259236.1","gene_symbol":"GOLGA8VP","gene_name":"golgin A8 family member V, pseudogene [Source:HGNC Symbol;Acc:HGNC:49920]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441736","summary":null,"start":101771758,"end":101781989,"strand":-1,"description":"golgin A8 family member V, pseudogene [Source:HGNC Symbol;Acc:HGNC:49920]"}, {"versioned_ensembl_gene_id":"ENSG00000204022.9","gene_symbol":"LIPJ","gene_name":"lipase family member J [Source:HGNC Symbol;Acc:HGNC:21773]","synonyms":"LIPL1,bA425M17.2","biotype":"protein_coding","ncbi_id":"142910","summary":null,"start":88586753,"end":88606976,"strand":1,"description":"lipase family member J [Source:HGNC Symbol;Acc:HGNC:21773]"}, {"versioned_ensembl_gene_id":"ENSG00000259890.1","gene_symbol":"DNM1P50","gene_name":"dynamin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48499]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927579","summary":null,"start":30567822,"end":30571089,"strand":-1,"description":"dynamin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48499]"}, {"versioned_ensembl_gene_id":"ENSG00000100058.12","gene_symbol":"CRYBB2P1","gene_name":"crystallin beta B2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2399]","synonyms":"CRYB2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1416","summary":null,"start":25448105,"end":25520854,"strand":1,"description":"crystallin beta B2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2399]"}, {"versioned_ensembl_gene_id":"ENSG00000211805.1","gene_symbol":"TRAV24","gene_name":"T-cell receptor alpha variable 24 [Source:HGNC Symbol;Acc:HGNC:12121]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28659","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22105343,"end":22105846,"strand":1,"description":"T-cell receptor alpha variable 24 [Source:HGNC Symbol;Acc:HGNC:12121]"}, {"versioned_ensembl_gene_id":"ENSG00000278574.4","gene_symbol":"ZNHIT3","gene_name":"zinc finger HIT-type containing 3 [Source:HGNC Symbol;Acc:HGNC:12309]","synonyms":"TRIP3","biotype":"protein_coding","ncbi_id":"9326","summary":null,"start":36487001,"end":36499682,"strand":1,"description":"zinc finger HIT-type containing 3 [Source:HGNC Symbol;Acc:HGNC:12309]"}, {"versioned_ensembl_gene_id":"ENSG00000206346.8","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":31960187,"end":31962669,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000211792.2","gene_symbol":"TRAV14DV4","gene_name":"T-cell receptor alpha variable 14/delta variable 4 [Source:HGNC Symbol;Acc:HGNC:12110]","synonyms":"TRAV14/DV4,TCRAV6S1-hDV104S1,hADV14S1","biotype":"TR_V_gene","ncbi_id":"28669","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21924063,"end":21924651,"strand":1,"description":"T-cell receptor alpha variable 14/delta variable 4 [Source:HGNC Symbol;Acc:HGNC:12110]"}, {"versioned_ensembl_gene_id":"ENSG00000256071.1","gene_symbol":"AC084291.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117889454,"end":117891008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215193.12","gene_symbol":"PEX26","gene_name":"peroxisomal biogenesis factor 26 [Source:HGNC Symbol;Acc:HGNC:22965]","synonyms":"FLJ20695","biotype":"protein_coding","ncbi_id":"55670","summary":"This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]","start":18077920,"end":18131138,"strand":1,"description":"peroxisomal biogenesis factor 26 [Source:HGNC Symbol;Acc:HGNC:22965]"}, {"versioned_ensembl_gene_id":"ENSG00000111843.13","gene_symbol":"TMEM14C","gene_name":"transmembrane protein 14C [Source:HGNC Symbol;Acc:HGNC:20952]","synonyms":"NET26,HSPC194,C6orf53,bA421M1.6","biotype":"protein_coding","ncbi_id":"51522","summary":null,"start":10722915,"end":10731129,"strand":1,"description":"transmembrane protein 14C [Source:HGNC Symbol;Acc:HGNC:20952]"}, {"versioned_ensembl_gene_id":"ENSG00000253661.1","gene_symbol":"ZFHX4-AS1","gene_name":"ZFHX4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44165]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100192378","summary":null,"start":76491200,"end":76683278,"strand":-1,"description":"ZFHX4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44165]"}, {"versioned_ensembl_gene_id":"ENSG00000249692.1","gene_symbol":"AC009567.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154770568,"end":154770916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250902.1","gene_symbol":"SMAD1-AS1","gene_name":"SMAD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49379]","synonyms":"ENST00000513542","biotype":"antisense_RNA","ncbi_id":"104326058","summary":null,"start":145514615,"end":145517118,"strand":-1,"description":"SMAD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49379]"}, {"versioned_ensembl_gene_id":"ENSG00000138483.2","gene_symbol":"CCDC54","gene_name":"coiled-coil domain containing 54 [Source:HGNC Symbol;Acc:HGNC:30703]","synonyms":"FLJ25362,SP17,NYD-SP17","biotype":"protein_coding","ncbi_id":"84692","summary":null,"start":107377194,"end":107378637,"strand":1,"description":"coiled-coil domain containing 54 [Source:HGNC Symbol;Acc:HGNC:30703]"}, {"versioned_ensembl_gene_id":"ENSG00000230712.2","gene_symbol":"GGTLC4P","gene_name":"gamma-glutamyltransferase light chain 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33428]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729838","summary":null,"start":24248074,"end":24249466,"strand":-1,"description":"gamma-glutamyltransferase light chain 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33428]"}, {"versioned_ensembl_gene_id":"ENSG00000234714.1","gene_symbol":"AC009965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204090457,"end":204109849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235951.1","gene_symbol":"AC009965.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204065706,"end":204067363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236522.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30695318,"end":30705434,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000225271.1","gene_symbol":"AC074281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8980425,"end":8982505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170166.5","gene_symbol":"HOXD4","gene_name":"homeobox D4 [Source:HGNC Symbol;Acc:HGNC:5138]","synonyms":"HOX4,HOX4B","biotype":"protein_coding","ncbi_id":"3233","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The protein encoded by this gene may play a role in determining positional values in developing limb buds. Alternatively spliced variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":176151222,"end":176153226,"strand":1,"description":"homeobox D4 [Source:HGNC Symbol;Acc:HGNC:5138]"}, {"versioned_ensembl_gene_id":"ENSG00000224424.7","gene_symbol":"PRKAR2A-AS1","gene_name":"PRKAR2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40471]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506637","summary":null,"start":48847572,"end":48851981,"strand":1,"description":"PRKAR2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40471]"}, {"versioned_ensembl_gene_id":"ENSG00000227624.2","gene_symbol":"SNRPEP3","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43445]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129329","summary":null,"start":20238972,"end":20239247,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43445]"}, {"versioned_ensembl_gene_id":"ENSG00000162104.9","gene_symbol":"ADCY9","gene_name":"adenylate cyclase 9 [Source:HGNC Symbol;Acc:HGNC:240]","synonyms":"AC9","biotype":"protein_coding","ncbi_id":"115","summary":"Adenylate cyclase is a membrane bound enzyme that catalyses the formation of cyclic AMP from ATP. It is regulated by a family of G protein-coupled receptors, protein kinases, and calcium. The type 9 adenylyl cyclase is a widely distributed adenylyl cyclase, and it is stimulated by beta-adrenergic receptor activation but is insensitive to forskolin, calcium, and somatostatin. [provided by RefSeq, Jul 2008]","start":3953387,"end":4116185,"strand":-1,"description":"adenylate cyclase 9 [Source:HGNC Symbol;Acc:HGNC:240]"}, {"versioned_ensembl_gene_id":"ENSG00000077097.15","gene_symbol":"TOP2B","gene_name":"topoisomerase (DNA) II beta [Source:HGNC Symbol;Acc:HGNC:11990]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7155","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional stress that occurs during DNA transcription and replication. It catalyzes the transient breaking and rejoining of two strands of duplex DNA which allows the strands to pass through one another, thus altering the topology of DNA. Two forms of this enzyme exist as likely products of a gene duplication event. The gene encoding this form, beta, is localized to chromosome 3 and the alpha form is localized to chromosome 17. The gene encoding this enzyme functions as the target for several anticancer agents and a variety of mutations in this gene have been associated with the development of drug resistance. Reduced activity of this enzyme may also play a role in ataxia-telangiectasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":25597905,"end":25664907,"strand":-1,"description":"topoisomerase (DNA) II beta [Source:HGNC Symbol;Acc:HGNC:11990]"}, {"versioned_ensembl_gene_id":"ENSG00000157110.15","gene_symbol":"RBPMS","gene_name":"RNA binding protein with multiple splicing [Source:HGNC Symbol;Acc:HGNC:19097]","synonyms":"HERMES","biotype":"protein_coding","ncbi_id":"11030","summary":"This gene encodes a member of the RNA recognition motif family of RNA-binding proteins. The RNA recognition motif is between 80-100 amino acids in length and family members contain one to four copies of the motif. The RNA recognition motif consists of two short stretches of conserved sequence, as well as a few highly conserved hydrophobic residues. The encoded protein has a single, putative RNA recognition motif in its N-terminus. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]","start":30384479,"end":30572261,"strand":1,"description":"RNA binding protein with multiple splicing [Source:HGNC Symbol;Acc:HGNC:19097]"}, {"versioned_ensembl_gene_id":"ENSG00000254316.1","gene_symbol":"AC090820.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30249502,"end":30250092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271952.1","gene_symbol":"LINC01954","gene_name":"long intergenic non-protein coding RNA 1954 [Source:HGNC Symbol;Acc:HGNC:52779]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929733","summary":null,"start":10878269,"end":10885118,"strand":1,"description":"long intergenic non-protein coding RNA 1954 [Source:HGNC Symbol;Acc:HGNC:52779]"}, {"versioned_ensembl_gene_id":"ENSG00000248159.1","gene_symbol":"HSPA8P11","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:44926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392209","summary":null,"start":30237382,"end":30240997,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:44926]"}, {"versioned_ensembl_gene_id":"ENSG00000232343.1","gene_symbol":"BX248406.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32809613,"end":32810443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280946.1","gene_symbol":"CR854858.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13076471,"end":13079295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257941.1","gene_symbol":"AC011611.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76057538,"end":76058115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089682.16","gene_symbol":"RBM41","gene_name":"RNA binding motif protein 41 [Source:HGNC Symbol;Acc:HGNC:25617]","synonyms":"FLJ11016","biotype":"protein_coding","ncbi_id":"55285","summary":null,"start":107064420,"end":107118823,"strand":-1,"description":"RNA binding motif protein 41 [Source:HGNC Symbol;Acc:HGNC:25617]"}, {"versioned_ensembl_gene_id":"ENSG00000234840.1","gene_symbol":"LINC01239","gene_name":"long intergenic non-protein coding RNA 1239 [Source:HGNC Symbol;Acc:HGNC:49796]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441389","summary":null,"start":22646200,"end":22824213,"strand":1,"description":"long intergenic non-protein coding RNA 1239 [Source:HGNC Symbol;Acc:HGNC:49796]"}, {"versioned_ensembl_gene_id":"ENSG00000224549.1","gene_symbol":"AC017067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22767175,"end":22768316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228568.1","gene_symbol":"AC006461.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72288785,"end":72289110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223517.1","gene_symbol":"AC010723.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14276212,"end":14277489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188660.3","gene_symbol":"LINC00319","gene_name":"long intergenic non-protein coding RNA 319 [Source:HGNC Symbol;Acc:HGNC:19730]","synonyms":"PRED49,NCRNA00319,FLJ38036,C21orf125","biotype":"lincRNA","ncbi_id":"284836","summary":null,"start":43446601,"end":43453893,"strand":1,"description":"long intergenic non-protein coding RNA 319 [Source:HGNC Symbol;Acc:HGNC:19730]"}, {"versioned_ensembl_gene_id":"ENSG00000281828.1","gene_symbol":"AC136687.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22482318,"end":22486719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121005.8","gene_symbol":"CRISPLD1","gene_name":"cysteine rich secretory protein LCCL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18206]","synonyms":"LCRISP1,DKFZp762F133,Cocoacrisp","biotype":"protein_coding","ncbi_id":"83690","summary":null,"start":74984515,"end":75034558,"strand":1,"description":"cysteine rich secretory protein LCCL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18206]"}, {"versioned_ensembl_gene_id":"ENSG00000254238.1","gene_symbol":"AC100782.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75026428,"end":75029460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107625.12","gene_symbol":"DDX50","gene_name":"DExD-box helicase 50 [Source:HGNC Symbol;Acc:HGNC:17906]","synonyms":"RH-II/GuB,MGC3199,GUB,GU2","biotype":"protein_coding","ncbi_id":"79009","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box enzyme that may be involved in ribosomal RNA synthesis or processing. This gene and DDX21, also called RH-II/GuA, have similar genomic structures and are in tandem orientation on chromosome 10, suggesting that the two genes arose by gene duplication in evolution. This gene has pseudogenes on chromosomes 2, 3 and 4. Alternative splicing of this gene generates multiple transcript variants, but the full length nature of all the other variants but one has not been defined. [provided by RefSeq, Jul 2008]","start":68901278,"end":68946847,"strand":1,"description":"DExD-box helicase 50 [Source:HGNC Symbol;Acc:HGNC:17906]"}, {"versioned_ensembl_gene_id":"ENSG00000137384.12","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"ZNF178,RNF93,ZNFB7","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30152741,"end":30162231,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000228213.5","gene_symbol":"NLGN1-AS1","gene_name":"NLGN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40676]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874010","summary":null,"start":173910498,"end":173920796,"strand":-1,"description":"NLGN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40676]"}, {"versioned_ensembl_gene_id":"ENSG00000282681.1","gene_symbol":"AC083982.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143012485,"end":143018437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235469.1","gene_symbol":"MRPL50P4","gene_name":"mitochondrial ribosomal protein L50 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29722]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359751","summary":null,"start":59551404,"end":59551878,"strand":-1,"description":"mitochondrial ribosomal protein L50 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29722]"}, {"versioned_ensembl_gene_id":"ENSG00000132849.19","gene_symbol":"PATJ","gene_name":"PATJ, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:28881]","synonyms":"INADL,Cipp","biotype":"protein_coding","ncbi_id":"10207","summary":"This gene encodes a protein with multiple PDZ domains. PDZ domains mediate protein-protein interactions, and proteins with multiple PDZ domains often organize multimeric complexes at the plasma membrane. This protein localizes to tight junctions and to the apical membrane of epithelial cells. A similar protein in Drosophila is a scaffolding protein which tethers several members of a multimeric signaling complex in photoreceptors. [provided by RefSeq, Jul 2008]","start":61742477,"end":62178675,"strand":1,"description":"PATJ, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:28881]"}, {"versioned_ensembl_gene_id":"ENSG00000236646.1","gene_symbol":"LAMTOR5P1","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31854]","synonyms":"HBXIPP1,HBXIPL","biotype":"processed_pseudogene","ncbi_id":"106478910","summary":null,"start":62038842,"end":62039111,"strand":1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31854]"}, {"versioned_ensembl_gene_id":"ENSG00000237536.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"HTATSF1P,dJ1033B10.6,TAT-SF1-L","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33159435,"end":33161326,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000268623.2","gene_symbol":"AC020904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18040355,"end":18041083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260219.2","gene_symbol":"AC106782.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30355441,"end":30357104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274653.1","gene_symbol":"AC106782.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30359825,"end":30360336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255495.1","gene_symbol":"AC145124.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12194467,"end":12196280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231729.1","gene_symbol":"ARHGEF9-IT1","gene_name":"ARHGEF9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41401]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874355","summary":null,"start":63670196,"end":63671502,"strand":-1,"description":"ARHGEF9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41401]"}, {"versioned_ensembl_gene_id":"ENSG00000236836.1","gene_symbol":"PCYT1B-AS1","gene_name":"PCYT1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40431]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874088","summary":null,"start":24650073,"end":24658237,"strand":1,"description":"PCYT1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40431]"}, {"versioned_ensembl_gene_id":"ENSG00000249745.1","gene_symbol":"HMGB1P28","gene_name":"high mobility group box 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39119]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133310","summary":null,"start":41842154,"end":41843950,"strand":-1,"description":"high mobility group box 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39119]"}, {"versioned_ensembl_gene_id":"ENSG00000116489.12","gene_symbol":"CAPZA1","gene_name":"capping actin protein of muscle Z-line alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:1488]","synonyms":null,"biotype":"protein_coding","ncbi_id":"829","summary":"CAPZA1 is a member of the F-actin capping protein alpha subunit family. This gene encodes the alpha subunit of the barbed-end actin binding protein. The protein regulates growth of the actin filament by capping the barbed end of growing actin filaments. [provided by RefSeq, Jul 2008]","start":112619173,"end":112671619,"strand":1,"description":"capping actin protein of muscle Z-line alpha subunit 1 [Source:HGNC Symbol;Acc:HGNC:1488]"}, {"versioned_ensembl_gene_id":"ENSG00000236165.1","gene_symbol":"PRADC1P1","gene_name":"protease associated domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44534]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645571","summary":null,"start":36976316,"end":36976840,"strand":1,"description":"protease associated domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44534]"}, {"versioned_ensembl_gene_id":"ENSG00000170579.16","gene_symbol":"DLGAP1","gene_name":"DLG associated protein 1 [Source:HGNC Symbol;Acc:HGNC:2905]","synonyms":"SAPAP1,GKAP,DAP-1","biotype":"protein_coding","ncbi_id":"9229","summary":null,"start":3496032,"end":4455335,"strand":-1,"description":"DLG associated protein 1 [Source:HGNC Symbol;Acc:HGNC:2905]"}, {"versioned_ensembl_gene_id":"ENSG00000142611.16","gene_symbol":"PRDM16","gene_name":"PR/SET domain 16 [Source:HGNC Symbol;Acc:HGNC:14000]","synonyms":"PFM13,MGC166915,MEL1,KMT8F,KIAA1675","biotype":"protein_coding","ncbi_id":"63976","summary":"The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":3069168,"end":3438621,"strand":1,"description":"PR/SET domain 16 [Source:HGNC Symbol;Acc:HGNC:14000]"}, {"versioned_ensembl_gene_id":"ENSG00000226286.1","gene_symbol":"AL008733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3132927,"end":3133709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223631.1","gene_symbol":"LINC01120","gene_name":"long intergenic non-protein coding RNA 1120 [Source:HGNC Symbol;Acc:HGNC:49265]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389043","summary":null,"start":131402901,"end":131409049,"strand":1,"description":"long intergenic non-protein coding RNA 1120 [Source:HGNC Symbol;Acc:HGNC:49265]"}, {"versioned_ensembl_gene_id":"ENSG00000276460.1","gene_symbol":"AC073869.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131398439,"end":131401250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271379.1","gene_symbol":"AC023513.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42069935,"end":42070625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259685.2","gene_symbol":"AC092769.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90102649,"end":90133445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259892.1","gene_symbol":"AC027139.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34555870,"end":34556820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257858.1","gene_symbol":"MTND1P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42073]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873341","summary":null,"start":41699391,"end":41700251,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42073]"}, {"versioned_ensembl_gene_id":"ENSG00000241593.5","gene_symbol":"AC099542.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81246579,"end":81297345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087842.10","gene_symbol":"PIR","gene_name":"pirin [Source:HGNC Symbol;Acc:HGNC:30048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8544","summary":"This gene encodes a member of the cupin superfamily. The encoded protein is an Fe(II)-containing nuclear protein expressed in all tissues of the body and concentrated within dot-like subnuclear structures. Interactions with nuclear factor I/CCAAT box transcription factor as well as B cell lymphoma 3-encoded oncoprotein suggest the encoded protein may act as a transcriptional cofactor and be involved in the regulation of DNA transcription and replication. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]","start":15384799,"end":15493564,"strand":-1,"description":"pirin [Source:HGNC Symbol;Acc:HGNC:30048]"}, {"versioned_ensembl_gene_id":"ENSG00000110844.13","gene_symbol":"PRPF40B","gene_name":"pre-mRNA processing factor 40 homolog B [Source:HGNC Symbol;Acc:HGNC:25031]","synonyms":"HYPC","biotype":"protein_coding","ncbi_id":"25766","summary":"This gene encodes a WW-domain containing protein similar to yeast splicing factor PRP40. This protein has been shown to interact with Huntingtin and methyl CpG binding protein 2 (MeCP2). Alternative splicing results in different transcript variants. [provided by RefSeq, Aug 2014]","start":49568218,"end":49644666,"strand":1,"description":"pre-mRNA processing factor 40 homolog B [Source:HGNC Symbol;Acc:HGNC:25031]"}, {"versioned_ensembl_gene_id":"ENSG00000260913.1","gene_symbol":"LINC01254","gene_name":"long intergenic non-protein coding RNA 1254 [Source:HGNC Symbol;Acc:HGNC:49870]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927350","summary":null,"start":10405133,"end":10414515,"strand":-1,"description":"long intergenic non-protein coding RNA 1254 [Source:HGNC Symbol;Acc:HGNC:49870]"}, {"versioned_ensembl_gene_id":"ENSG00000282384.1","gene_symbol":"AC015849.11","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35808489,"end":35808897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157827.19","gene_symbol":"FMNL2","gene_name":"formin like 2 [Source:HGNC Symbol;Acc:HGNC:18267]","synonyms":"KIAA1902,FHOD2","biotype":"protein_coding","ncbi_id":"114793","summary":"This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. Alternatively spliced transcript variants encoding different isoforms have been described but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]","start":152335237,"end":152649834,"strand":1,"description":"formin like 2 [Source:HGNC Symbol;Acc:HGNC:18267]"}, {"versioned_ensembl_gene_id":"ENSG00000238076.1","gene_symbol":"MRPL48P1","gene_name":"mitochondrial ribosomal protein L48 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21379]","synonyms":"MRPL48L1,dJ290I10.4","biotype":"processed_pseudogene","ncbi_id":"221717","summary":null,"start":10459906,"end":10460541,"strand":-1,"description":"mitochondrial ribosomal protein L48 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21379]"}, {"versioned_ensembl_gene_id":"ENSG00000234241.1","gene_symbol":"AL109618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6213699,"end":6215381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243368.2","gene_symbol":"MCCC1-AS1","gene_name":"MCCC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40366]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480736","summary":null,"start":183016255,"end":183017808,"strand":1,"description":"MCCC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40366]"}, {"versioned_ensembl_gene_id":"ENSG00000224081.8","gene_symbol":"SLC44A3-AS1","gene_name":"SLC44A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49057]","synonyms":"LINC01057","biotype":"transcribed_processed_pseudogene","ncbi_id":"101928079","summary":null,"start":94613814,"end":94855426,"strand":-1,"description":"SLC44A3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49057]"}, {"versioned_ensembl_gene_id":"ENSG00000234890.1","gene_symbol":"HNRNPDLP2","gene_name":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48753]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128061","summary":null,"start":158419955,"end":158425303,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48753]"}, {"versioned_ensembl_gene_id":"ENSG00000273106.1","gene_symbol":"AC019129.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44167625,"end":44168859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117560.7","gene_symbol":"FASLG","gene_name":"Fas ligand [Source:HGNC Symbol;Acc:HGNC:11936]","synonyms":"CD178,APT1LG1,TNFSF6,FasL","biotype":"protein_coding","ncbi_id":"356","summary":"This gene is a member of the tumor necrosis factor superfamily. The primary function of the encoded transmembrane protein is the induction of apoptosis triggered by binding to FAS. The FAS/FASLG signaling pathway is essential for immune system regulation, including activation-induced cell death (AICD) of T cells and cytotoxic T lymphocyte induced cell death. It has also been implicated in the progression of several cancers. Defects in this gene may be related to some cases of systemic lupus erythematosus (SLE). Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2014]","start":172659018,"end":172666874,"strand":1,"description":"Fas ligand [Source:HGNC Symbol;Acc:HGNC:11936]"}, {"versioned_ensembl_gene_id":"ENSG00000257243.1","gene_symbol":"AC020612.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49595148,"end":49595688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262516.1","gene_symbol":"AC007151.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3840528,"end":3841010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170959.14","gene_symbol":"DCDC1","gene_name":"doublecortin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20625]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341019","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene is a hydrophilic, intracellular protein. It contains a single doublecortin domain and is unable to bind microtubules and to regulate microtubule polymerization. This gene is mainly expressed in adult testis. It does not have a mouse homolog. [provided by RefSeq, Sep 2010]","start":30830369,"end":31369810,"strand":-1,"description":"doublecortin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20625]"}, {"versioned_ensembl_gene_id":"ENSG00000233549.2","gene_symbol":"CYCSP35","gene_name":"cytochrome c, somatic pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:24409]","synonyms":"HCP35,HC8","biotype":"processed_pseudogene","ncbi_id":"121916","summary":null,"start":98629686,"end":98629989,"strand":-1,"description":"cytochrome c, somatic pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:24409]"}, {"versioned_ensembl_gene_id":"ENSG00000268473.1","gene_symbol":"AC092327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86434830,"end":86435884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065665.20","gene_symbol":"SEC61A2","gene_name":"Sec61 translocon alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:17702]","synonyms":"FLJ10578","biotype":"protein_coding","ncbi_id":"55176","summary":"The protein encoded by this gene has similarity to a mouse protein which suggests a role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum. It may also be required for the assembly of membrane and secretory proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":12129637,"end":12169961,"strand":1,"description":"Sec61 translocon alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:17702]"}, {"versioned_ensembl_gene_id":"ENSG00000103723.12","gene_symbol":"AP3B2","gene_name":"adaptor related protein complex 3 beta 2 subunit [Source:HGNC Symbol;Acc:HGNC:567]","synonyms":"NAPTB","biotype":"protein_coding","ncbi_id":"8120","summary":"Adaptor protein complex 3 (AP-3 complex) is a heterotrimeric protein complex involved in the formation of clathrin-coated synaptic vesicles. The protein encoded by this gene represents the beta subunit of the neuron-specific AP-3 complex and was first identified as the target antigen in human paraneoplastic neurologic disorders. The encoded subunit binds clathrin and is phosphorylated by a casein kinase-like protein, which mediates synaptic vesicle coat assembly. Defects in this gene are a cause of early-onset epileptic encephalopathy. [provided by RefSeq, Feb 2017]","start":82659281,"end":82709914,"strand":-1,"description":"adaptor related protein complex 3 beta 2 subunit [Source:HGNC Symbol;Acc:HGNC:567]"}, {"versioned_ensembl_gene_id":"ENSG00000101194.17","gene_symbol":"SLC17A9","gene_name":"solute carrier family 17 member 9 [Source:HGNC Symbol;Acc:HGNC:16192]","synonyms":"VNUT,FLJ23412,C20orf59","biotype":"protein_coding","ncbi_id":"63910","summary":"This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":62952647,"end":62969585,"strand":1,"description":"solute carrier family 17 member 9 [Source:HGNC Symbol;Acc:HGNC:16192]"}, {"versioned_ensembl_gene_id":"ENSG00000163795.13","gene_symbol":"ZNF513","gene_name":"zinc finger protein 513 [Source:HGNC Symbol;Acc:HGNC:26498]","synonyms":"RP58,FLJ32203","biotype":"protein_coding","ncbi_id":"130557","summary":"The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":27377231,"end":27380790,"strand":-1,"description":"zinc finger protein 513 [Source:HGNC Symbol;Acc:HGNC:26498]"}, {"versioned_ensembl_gene_id":"ENSG00000215208.3","gene_symbol":"KRT18P60","gene_name":"keratin 18 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48887]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418829","summary":null,"start":65418731,"end":65420027,"strand":-1,"description":"keratin 18 pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:48887]"}, {"versioned_ensembl_gene_id":"ENSG00000229102.1","gene_symbol":"AC076966.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179101366,"end":179147973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221855.1","gene_symbol":"TAS2R41","gene_name":"taste 2 receptor member 41 [Source:HGNC Symbol;Acc:HGNC:18883]","synonyms":"T2R59","biotype":"protein_coding","ncbi_id":"259287","summary":"This gene encodes a member of the bitter taste receptor family which belong to the G protein-coupled receptor superfamily and are predominantly expressed in taste receptor cells of the tongue and palate epithelia. This intronless taste receptor gene encodes a seven-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered together with eight other taste receptor genes on chromosome 7. Chloramphenicol is an agonist for the encoded protein. [provided by RefSeq, Jul 2017]","start":143477873,"end":143478796,"strand":1,"description":"taste 2 receptor member 41 [Source:HGNC Symbol;Acc:HGNC:18883]"}, {"versioned_ensembl_gene_id":"ENSG00000237402.1","gene_symbol":"CAMTA1-IT1","gene_name":"CAMTA1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41446]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874340","summary":null,"start":7368942,"end":7370270,"strand":1,"description":"CAMTA1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41446]"}, {"versioned_ensembl_gene_id":"ENSG00000226171.6","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DBP2,Prp2,DDX16,PRPF2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30645335,"end":30665285,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000187583.10","gene_symbol":"PLEKHN1","gene_name":"pleckstrin homology domain containing N1 [Source:HGNC Symbol;Acc:HGNC:25284]","synonyms":"DKFZP434H2010","biotype":"protein_coding","ncbi_id":"84069","summary":null,"start":966497,"end":975865,"strand":1,"description":"pleckstrin homology domain containing N1 [Source:HGNC Symbol;Acc:HGNC:25284]"}, {"versioned_ensembl_gene_id":"ENSG00000117758.13","gene_symbol":"STX12","gene_name":"syntaxin 12 [Source:HGNC Symbol;Acc:HGNC:11430]","synonyms":"STX14,STX13","biotype":"protein_coding","ncbi_id":"23673","summary":null,"start":27773183,"end":27824452,"strand":1,"description":"syntaxin 12 [Source:HGNC Symbol;Acc:HGNC:11430]"}, {"versioned_ensembl_gene_id":"ENSG00000226017.2","gene_symbol":"PRICKLE2-AS3","gene_name":"PRICKLE2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40918]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874243","summary":null,"start":64187544,"end":64200965,"strand":1,"description":"PRICKLE2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40918]"}, {"versioned_ensembl_gene_id":"ENSG00000189064.8","gene_symbol":"GAGE2A","gene_name":"G antigen 2A [Source:HGNC Symbol;Acc:HGNC:4099]","synonyms":"CT4.2,GAGE2","biotype":"protein_coding","ncbi_id":"729447","summary":null,"start":49589529,"end":49596827,"strand":1,"description":"G antigen 2A [Source:HGNC Symbol;Acc:HGNC:4099]"}, {"versioned_ensembl_gene_id":"ENSG00000151914.19","gene_symbol":"DST","gene_name":"dystonin [Source:HGNC Symbol;Acc:HGNC:1090]","synonyms":"FLJ13425,CATX-15,BPAG1,BPA,BP240,MACF2,KIAA0728,FLJ32235,FLJ30627,FLJ21489","biotype":"protein_coding","ncbi_id":"667","summary":"This gene encodes a member of the plakin protein family of adhesion junction plaque proteins. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the full-length nature of some variants has not been defined. It has been reported that some isoforms are expressed in neural and muscle tissue, anchoring neural intermediate filaments to the actin cytoskeleton, and some isoforms are expressed in epithelial tissue, anchoring keratin-containing intermediate filaments to hemidesmosomes. Consistent with the expression, mice defective for this gene show skin blistering and neurodegeneration. [provided by RefSeq, Mar 2010]","start":56457987,"end":56954628,"strand":-1,"description":"dystonin [Source:HGNC Symbol;Acc:HGNC:1090]"}, {"versioned_ensembl_gene_id":"ENSG00000231173.1","gene_symbol":"AC116609.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":741977,"end":749856,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100345.20","gene_symbol":"MYH9","gene_name":"myosin heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:7579]","synonyms":"NMMHCA,NMHC-II-A,MHA,FTNS,EPSTS,DFNA17","biotype":"protein_coding","ncbi_id":"4627","summary":"This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]","start":36281281,"end":36388018,"strand":-1,"description":"myosin heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:7579]"}, {"versioned_ensembl_gene_id":"ENSG00000258464.1","gene_symbol":"AL160237.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23729038,"end":23729741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231619.1","gene_symbol":"AC003685.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8856665,"end":8857059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265554.1","gene_symbol":"AP005271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10125340,"end":10144406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163637.12","gene_symbol":"PRICKLE2","gene_name":"prickle planar cell polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:20340]","synonyms":"DKFZp686D143","biotype":"protein_coding","ncbi_id":"166336","summary":"This gene encodes a homolog of Drosophila prickle. The exact function of this gene is not known, however, studies in mice suggest that it may be involved in seizure prevention. Mutations in this gene are associated with progressive myoclonic epilepsy type 5. [provided by RefSeq, Dec 2011]","start":64092242,"end":64445476,"strand":-1,"description":"prickle planar cell polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:20340]"}, {"versioned_ensembl_gene_id":"ENSG00000282638.1","gene_symbol":"AC243742.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15786391,"end":15787272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189196.4","gene_symbol":"LINC00994","gene_name":"long intergenic non-protein coding RNA 994 [Source:HGNC Symbol;Acc:HGNC:48949]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287879","summary":null,"start":64078361,"end":64087363,"strand":-1,"description":"long intergenic non-protein coding RNA 994 [Source:HGNC Symbol;Acc:HGNC:48949]"}, {"versioned_ensembl_gene_id":"ENSG00000270604.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"lincRNA","ncbi_id":"414778","summary":null,"start":30234039,"end":30326134,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000236475.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30238301,"end":30242279,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000165376.10","gene_symbol":"CLDN2","gene_name":"claudin 2 [Source:HGNC Symbol;Acc:HGNC:2041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9075","summary":"This gene product belongs to the claudin protein family whose members have been identified as major integral membrane proteins localized exclusively at tight junctions. Claudins are expressed in an organ-specific manner and regulate tissue-specific physiologic properties of tight junctions. This protein is expressed in the intestine. Alternatively spliced transcript variants with different 5' untranslated region have been found for this gene.[provided by RefSeq, Jan 2010]","start":106900164,"end":106930861,"strand":1,"description":"claudin 2 [Source:HGNC Symbol;Acc:HGNC:2041]"}, {"versioned_ensembl_gene_id":"ENSG00000206069.6","gene_symbol":"TMEM211","gene_name":"transmembrane protein 211 [Source:HGNC Symbol;Acc:HGNC:33725]","synonyms":"bA9F11.1","biotype":"protein_coding","ncbi_id":"255349","summary":null,"start":24934954,"end":24946695,"strand":-1,"description":"transmembrane protein 211 [Source:HGNC Symbol;Acc:HGNC:33725]"}, {"versioned_ensembl_gene_id":"ENSG00000196566.2","gene_symbol":"AL138767.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87610163,"end":87660003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248636.6","gene_symbol":"AC002070.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119387987,"end":119668079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231601.1","gene_symbol":"AL157709.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":743992,"end":744958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257199.2","gene_symbol":"AC025161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76984079,"end":76984669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267762.1","gene_symbol":"AC048380.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48673575,"end":48688419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231158.1","gene_symbol":"PTP4A1P1","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421652","summary":null,"start":158065545,"end":158066059,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41928]"}, {"versioned_ensembl_gene_id":"ENSG00000228937.1","gene_symbol":"AC005539.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157961410,"end":157962888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260673.1","gene_symbol":"AL034376.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4599287,"end":4602420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188856.6","gene_symbol":"RPSAP47","gene_name":"ribosomal protein SA pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36162]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389672","summary":"Although this locus has an open reading frame that could produce a protein of the same or nearly the same size as that of the RPSA gene, there is no convincing evidence of transcription. It is thus being annotated as a pseudogene.[provided by RefSeq, Feb 2009]","start":80558870,"end":80559757,"strand":1,"description":"ribosomal protein SA pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:36162]"}, {"versioned_ensembl_gene_id":"ENSG00000163681.14","gene_symbol":"SLMAP","gene_name":"sarcolemma associated protein [Source:HGNC Symbol;Acc:HGNC:16643]","synonyms":"SLAP,KIAA1601","biotype":"protein_coding","ncbi_id":"7871","summary":"This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":57755450,"end":57929168,"strand":1,"description":"sarcolemma associated protein [Source:HGNC Symbol;Acc:HGNC:16643]"}, {"versioned_ensembl_gene_id":"ENSG00000134030.13","gene_symbol":"CTIF","gene_name":"cap binding complex dependent translation initiation factor [Source:HGNC Symbol;Acc:HGNC:23925]","synonyms":"KIAA0427","biotype":"protein_coding","ncbi_id":"9811","summary":"CTIF is a component of the CBP80 (NCBP1; MIM 600469)/CBP20 (NCBP2; MIM 605133) translation initiation complex that binds cotranscriptionally to the cap end of nascent mRNA. The CBP80/CBP20 complex is involved in a simultaneous editing and translation step that recognizes premature termination codons (PTCs) in mRNAs and directs PTC-containing mRNAs toward nonsense-mediated decay (NMD). On mRNAs without PTCs, the CBP80/CBP20 complex is replaced with cytoplasmic mRNA cap-binding proteins, including EIF4G (MIM 600495), and steady-state translation of the mRNAs resumes in the cytoplasm (Kim et al., 2009 [PubMed 19648179]).[supplied by OMIM, Dec 2009]","start":48539046,"end":48863217,"strand":1,"description":"cap binding complex dependent translation initiation factor [Source:HGNC Symbol;Acc:HGNC:23925]"}, {"versioned_ensembl_gene_id":"ENSG00000240535.8","gene_symbol":"AC034238.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":55021299,"end":55042844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167693.16","gene_symbol":"NXN","gene_name":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]","synonyms":"NRX,FLJ12614","biotype":"protein_coding","ncbi_id":"64359","summary":"This gene encodes a member of the thioredoxin superfamily, a group of small, multifunctional redox-active proteins. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. The encoded protein acts a redox-dependent regulator of the Wnt signaling pathway and is involved in cell growth and differentiation. [provided by RefSeq, Sep 2015]","start":799313,"end":979770,"strand":-1,"description":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]"}, {"versioned_ensembl_gene_id":"ENSG00000127399.14","gene_symbol":"LRRC61","gene_name":"leucine rich repeat containing 61 [Source:HGNC Symbol;Acc:HGNC:21704]","synonyms":"MGC3036,HSPC295,FLJ31392","biotype":"protein_coding","ncbi_id":"65999","summary":null,"start":150322639,"end":150338150,"strand":1,"description":"leucine rich repeat containing 61 [Source:HGNC Symbol;Acc:HGNC:21704]"}, {"versioned_ensembl_gene_id":"ENSG00000171791.12","gene_symbol":"BCL2","gene_name":"BCL2, apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:990]","synonyms":"PPP1R50,Bcl-2","biotype":"protein_coding","ncbi_id":"596","summary":"This gene encodes an integral outer mitochondrial membrane protein that blocks the apoptotic death of some cells such as lymphocytes. Constitutive expression of BCL2, such as in the case of translocation of BCL2 to Ig heavy chain locus, is thought to be the cause of follicular lymphoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":63123346,"end":63320128,"strand":-1,"description":"BCL2, apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:990]"}, {"versioned_ensembl_gene_id":"ENSG00000181467.4","gene_symbol":"RAP2B","gene_name":"RAP2B, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9862]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5912","summary":"This intronless gene belongs to a family of RAS-related genes. The proteins encoded by these genes share approximately 50% amino acid identity with the classical RAS proteins and have numerous structural features in common. The most striking difference between the RAP and RAS proteins resides in their 61st amino acid: glutamine in RAS is replaced by threonine in RAP proteins. Evidence suggests that this protein may be polyisoprenylated and palmitoylated. [provided by RefSeq, Jul 2008]","start":153162270,"end":153170620,"strand":1,"description":"RAP2B, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9862]"}, {"versioned_ensembl_gene_id":"ENSG00000115170.13","gene_symbol":"ACVR1","gene_name":"activin A receptor type 1 [Source:HGNC Symbol;Acc:HGNC:171]","synonyms":"ACVRLK2,ACVR1A,SKR1,ALK2","biotype":"protein_coding","ncbi_id":"90","summary":"Activins are dimeric growth and differentiation factors which belong to the transforming growth factor-beta (TGF-beta) superfamily of structurally related signaling proteins. Activins signal through a heteromeric complex of receptor serine kinases which include at least two type I ( I and IB) and two type II (II and IIB) receptors. These receptors are all transmembrane proteins, composed of a ligand-binding extracellular domain with cysteine-rich region, a transmembrane domain, and a cytoplasmic domain with predicted serine/threonine specificity. Type I receptors are essential for signaling; and type II receptors are required for binding ligands and for expression of type I receptors. Type I and II receptors form a stable complex after ligand binding, resulting in phosphorylation of type I receptors by type II receptors. This gene encodes activin A type I receptor which signals a particular transcriptional response in concert with activin type II receptors. Mutations in this gene are associated with fibrodysplasia ossificans progressive. [provided by RefSeq, Jul 2008]","start":157736444,"end":157875862,"strand":-1,"description":"activin A receptor type 1 [Source:HGNC Symbol;Acc:HGNC:171]"}, {"versioned_ensembl_gene_id":"ENSG00000228791.7","gene_symbol":"THRB-AS1","gene_name":"THRB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44515]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"644990","summary":null,"start":24494087,"end":24681711,"strand":1,"description":"THRB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44515]"}, {"versioned_ensembl_gene_id":"ENSG00000276938.3","gene_symbol":"AC073135.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198148759,"end":198166452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249686.1","gene_symbol":"AC108078.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69450014,"end":69451613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274112.2","gene_symbol":"SMDT1","gene_name":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]","synonyms":"dJ186O1.1,DDDD,C22orf32,EMRE","biotype":"protein_coding","ncbi_id":"91689","summary":"This gene encodes a core regulatory component of a calcium channel in the mitochondrial inner membrane. [provided by RefSeq, Apr 2017]","start":42079691,"end":42084284,"strand":1,"description":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]"}, {"versioned_ensembl_gene_id":"ENSG00000033030.13","gene_symbol":"ZCCHC8","gene_name":"zinc finger CCHC-type containing 8 [Source:HGNC Symbol;Acc:HGNC:25265]","synonyms":"DKFZp434E2220","biotype":"protein_coding","ncbi_id":"55596","summary":"This gene encodes a scaffold protein which serves as an assessory factor to the nuclear RNA exosome complex. The encoded protein forms a trimeric human nuclear exosome targeting (NEXT) complex, together with hMTR4 and the RNA-binding factor RBM7 which promotes the exosomal degradation of non-coding promoter-upstream transcripts, enhancer RNAs and 3'-extended products of histone- and small nuclear RNA transcription. This complex is also thought to recruit the exosome to degrade intronic RNAs via its interaction with both the exosome and the spliceosome. It contains both an N-terminal zinc-knuckle domain and a C-terminal proline-rich domain. [provided by RefSeq, Apr 2017]","start":122471600,"end":122501073,"strand":-1,"description":"zinc finger CCHC-type containing 8 [Source:HGNC Symbol;Acc:HGNC:25265]"}, {"versioned_ensembl_gene_id":"ENSG00000112511.17","gene_symbol":"PHF1","gene_name":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]","synonyms":"MTF2L2,TDRD19C,PCL1","biotype":"protein_coding","ncbi_id":"5252","summary":"This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":33410399,"end":33416453,"strand":1,"description":"PHD finger protein 1 [Source:HGNC Symbol;Acc:HGNC:8919]"}, {"versioned_ensembl_gene_id":"ENSG00000237365.1","gene_symbol":"AL512330.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7008376,"end":7014279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267857.2","gene_symbol":"AL133499.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45100487,"end":45101094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166734.18","gene_symbol":"CASC4","gene_name":"cancer susceptibility 4 [Source:HGNC Symbol;Acc:HGNC:24892]","synonyms":"DKFZp459F1927,H63","biotype":"protein_coding","ncbi_id":"113201","summary":"The increased expression level of this gene is associated with HER-2/neu proto-oncogene overexpression. Amplification and resulting overexpression of this proto-oncogene are found in approximately 30% of human breast and 20% of human ovarian cancers. Alternatively spliced variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Dec 2010]","start":44288729,"end":44415758,"strand":1,"description":"cancer susceptibility 4 [Source:HGNC Symbol;Acc:HGNC:24892]"}, {"versioned_ensembl_gene_id":"ENSG00000281496.1","gene_symbol":"AC073135.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":198177148,"end":198186438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274918.1","gene_symbol":"AC116447.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35317396,"end":35317848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230833.1","gene_symbol":"RPEP3","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44522]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420555","summary":null,"start":27739954,"end":27740629,"strand":1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44522]"}, {"versioned_ensembl_gene_id":"ENSG00000102313.8","gene_symbol":"ITIH6","gene_name":"inter-alpha-trypsin inhibitor heavy chain family member 6 [Source:HGNC Symbol;Acc:HGNC:28907]","synonyms":"UNQ6369,ITIH5L","biotype":"protein_coding","ncbi_id":"347365","summary":"The protein encoded by this gene belongs to the interalpha trypsin inhibitor heavy chain (ITIH) family. Interalpha trypsin inhibitor (ITI) is composed of two heavy chains (containing VWA domain) and one light chain. The light chain confers the protease-inhibitor function, while the heavy chains are involved in mediating protein-protein interactions with the components of the extracellular matrix. [provided by RefSeq, Sep 2009]","start":54748899,"end":54798240,"strand":-1,"description":"inter-alpha-trypsin inhibitor heavy chain family member 6 [Source:HGNC Symbol;Acc:HGNC:28907]"}, {"versioned_ensembl_gene_id":"ENSG00000204894.4","gene_symbol":"AC104692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152367171,"end":152367260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241007.1","gene_symbol":"SEPT7P6","gene_name":"septin 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38042]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418720","summary":null,"start":152367519,"end":152368661,"strand":1,"description":"septin 7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38042]"}, {"versioned_ensembl_gene_id":"ENSG00000183741.11","gene_symbol":"CBX6","gene_name":"chromobox 6 [Source:HGNC Symbol;Acc:HGNC:1556]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23466","summary":null,"start":38861450,"end":38872314,"strand":-1,"description":"chromobox 6 [Source:HGNC Symbol;Acc:HGNC:1556]"}, {"versioned_ensembl_gene_id":"ENSG00000170113.15","gene_symbol":"NIPA1","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 1 [Source:HGNC Symbol;Acc:HGNC:17043]","synonyms":"SPG6,MGC35570","biotype":"protein_coding","ncbi_id":"123606","summary":"This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]","start":22773063,"end":22829791,"strand":1,"description":"non imprinted in Prader-Willi/Angelman syndrome 1 [Source:HGNC Symbol;Acc:HGNC:17043]"}, {"versioned_ensembl_gene_id":"ENSG00000175170.14","gene_symbol":"FAM182B","gene_name":"family with sequence similarity 182 member B [Source:HGNC Symbol;Acc:HGNC:34503]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728882","summary":null,"start":25763466,"end":25868225,"strand":-1,"description":"family with sequence similarity 182 member B [Source:HGNC Symbol;Acc:HGNC:34503]"}, {"versioned_ensembl_gene_id":"ENSG00000259904.1","gene_symbol":"ACTG1P15","gene_name":"actin gamma 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:51495]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418951","summary":null,"start":34373541,"end":34374603,"strand":-1,"description":"actin gamma 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:51495]"}, {"versioned_ensembl_gene_id":"ENSG00000261178.2","gene_symbol":"AC009169.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60925733,"end":60928541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227167.1","gene_symbol":"AL442638.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18360597,"end":18362220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257534.1","gene_symbol":"AC023794.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54162065,"end":54164452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250742.2","gene_symbol":"LINC02381","gene_name":"long intergenic non-protein coding RNA 2381 [Source:HGNC Symbol;Acc:HGNC:53304]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400043","summary":null,"start":54126098,"end":54142493,"strand":1,"description":"long intergenic non-protein coding RNA 2381 [Source:HGNC Symbol;Acc:HGNC:53304]"}, {"versioned_ensembl_gene_id":"ENSG00000244486.8","gene_symbol":"SCARF2","gene_name":"scavenger receptor class F member 2 [Source:HGNC Symbol;Acc:HGNC:19869]","synonyms":"SREC2,SREC-II,HUMZD58C02","biotype":"protein_coding","ncbi_id":"91179","summary":"The protein encoded by this gene is similar to SCARF1/SREC-I, a scavenger receptor protein that mediates the binding and degradation of acetylated low density lipoprotein (Ac-LDL). This protein has only little activity of internalizing modified low density lipoproteins (LDL), but it can interact with SCARF1 through its extracellular domain. The association of this protein with SCARF1 is suppressed by the presence of scavenger ligands. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":20424815,"end":20437826,"strand":-1,"description":"scavenger receptor class F member 2 [Source:HGNC Symbol;Acc:HGNC:19869]"}, {"versioned_ensembl_gene_id":"ENSG00000239226.1","gene_symbol":"MRPS17P3","gene_name":"mitochondrial ribosomal protein S17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29736]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359757","summary":null,"start":78525101,"end":78525485,"strand":1,"description":"mitochondrial ribosomal protein S17 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29736]"}, {"versioned_ensembl_gene_id":"ENSG00000276649.1","gene_symbol":"AL117335.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1888128,"end":1894374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111729.14","gene_symbol":"CLEC4A","gene_name":"C-type lectin domain family 4 member A [Source:HGNC Symbol;Acc:HGNC:13257]","synonyms":"DDB27,DCIR,CLECSF6,CD367","biotype":"protein_coding","ncbi_id":"50856","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may play a role in inflammatory and immune response. Multiple transcript variants encoding distinct isoforms have been identified for this gene. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":8123632,"end":8138607,"strand":1,"description":"C-type lectin domain family 4 member A [Source:HGNC Symbol;Acc:HGNC:13257]"}, {"versioned_ensembl_gene_id":"ENSG00000283273.1","gene_symbol":"AC138649.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22714342,"end":22717727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277435.1","gene_symbol":"AC138649.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22690454,"end":22691158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275443.1","gene_symbol":"AC012409.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95990582,"end":96300990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272043.1","gene_symbol":"AC016405.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122780760,"end":122781071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109320.11","gene_symbol":"NFKB1","gene_name":"nuclear factor kappa B subunit 1 [Source:HGNC Symbol;Acc:HGNC:7794]","synonyms":"NFkappaB,NF-kB1,NF-kappaB,KBF1,p50,p105,NFKB-p50","biotype":"protein_coding","ncbi_id":"4790","summary":"This gene encodes a 105 kD protein which can undergo cotranslational processing by the 26S proteasome to produce a 50 kD protein. The 105 kD protein is a Rel protein-specific transcription inhibitor and the 50 kD protein is a DNA binding subunit of the NF-kappa-B (NFKB) protein complex. NFKB is a transcription regulator that is activated by various intra- and extra-cellular stimuli such as cytokines, oxidant-free radicals, ultraviolet irradiation, and bacterial or viral products. Activated NFKB translocates into the nucleus and stimulates the expression of genes involved in a wide variety of biological functions. Inappropriate activation of NFKB has been associated with a number of inflammatory diseases while persistent inhibition of NFKB leads to inappropriate immune cell development or delayed cell growth. NFKB is a critical regulator of the immediate-early response to viral infection. Alternative splicing results in multiple transcript variants encoding different isoforms, at least one of which is proteolytically processed. [provided by RefSeq, Aug 2020]","start":102501329,"end":102617302,"strand":1,"description":"nuclear factor kappa B subunit 1 [Source:HGNC Symbol;Acc:HGNC:7794]"}, {"versioned_ensembl_gene_id":"ENSG00000279645.1","gene_symbol":"AC016251.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96285068,"end":96289265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228039.3","gene_symbol":"AC253536.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23963780,"end":23964374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006747.14","gene_symbol":"SCIN","gene_name":"scinderin [Source:HGNC Symbol;Acc:HGNC:21695]","synonyms":"KIAA1905","biotype":"protein_coding","ncbi_id":"85477","summary":"SCIN is a Ca(2+)-dependent actin-severing and -capping protein (Zunino et al., 2001 [PubMed 11568009]).[supplied by OMIM, May 2010]","start":12570577,"end":12660179,"strand":1,"description":"scinderin [Source:HGNC Symbol;Acc:HGNC:21695]"}, {"versioned_ensembl_gene_id":"ENSG00000260317.1","gene_symbol":"AC009812.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80541300,"end":80543104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198704.9","gene_symbol":"GPX6","gene_name":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]","synonyms":"GPXP3,GPXP3","biotype":"protein_coding","ncbi_id":"257202","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. Expression of this gene has been observed in embryos and olfactory epithelium; however, the exact function of this gene is not known. This isozyme is a selenoprotein in humans, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. The orthologs of this gene in mouse and rat (and some other species) contain a cysteine (Cys) residue in place of the Sec residue, and their corresponding mRNAs lack SECIS element. [provided by RefSeq, Jul 2017]","start":28503296,"end":28528215,"strand":-1,"description":"glutathione peroxidase 6 [Source:HGNC Symbol;Acc:HGNC:4558]"}, {"versioned_ensembl_gene_id":"ENSG00000225606.1","gene_symbol":"AC005281.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12570125,"end":12571392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254162.1","gene_symbol":"AC009812.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80535006,"end":80539135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176454.13","gene_symbol":"LPCAT4","gene_name":"lysophosphatidylcholine acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:30059]","synonyms":"LPEAT2,LPAAT-eta,FLJ10257,AYTL3,AGPAT7","biotype":"protein_coding","ncbi_id":"254531","summary":"Members of the 1-acylglycerol-3-phosphate O-acyltransferase (EC 2.3.1.51) family, such as AGPAT7, catalyze the conversion of lysophosphatidic acid (LPA) to phosphatidic acid (PA), a precursor in the biosynthesis of all glycerolipids. Both LPA and PA are involved in signal transduction (Ye et al., 2005 [PubMed 16243729]).[supplied by OMIM, May 2008]","start":34358618,"end":34367278,"strand":-1,"description":"lysophosphatidylcholine acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:30059]"}, {"versioned_ensembl_gene_id":"ENSG00000073711.10","gene_symbol":"PPP2R3A","gene_name":"protein phosphatase 2 regulatory subunit B''alpha [Source:HGNC Symbol;Acc:HGNC:9307]","synonyms":"PR72,PR130,PPP2R3","biotype":"protein_coding","ncbi_id":"5523","summary":"This gene encodes one of the regulatory subunits of the protein phosphatase 2. Protein phosphatase 2 (formerly named type 2A) is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phosphatase 2 holoenzymes are heterotrimeric proteins composed of a structural subunit A, a catalytic subunit C, and a regulatory subunit B. The regulatory subunit is encoded by a diverse set of genes that have been grouped into the B/PR55, B'/PR61, and B''/PR72 families. These different regulatory subunits confer distinct enzymatic specificities and intracellular localizations to the holozenzyme. The product of this gene belongs to the B'' family. The B'' family has been further divided into subfamilies. The product of this gene belongs to the alpha subfamily of regulatory subunit B''. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Jun 2010]","start":135965673,"end":136147891,"strand":1,"description":"protein phosphatase 2 regulatory subunit B''alpha [Source:HGNC Symbol;Acc:HGNC:9307]"}, {"versioned_ensembl_gene_id":"ENSG00000278900.1","gene_symbol":"AC139792.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34105750,"end":34106336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180806.4","gene_symbol":"HOXC9","gene_name":"homeobox C9 [Source:HGNC Symbol;Acc:HGNC:5130]","synonyms":"HOX3B,HOX3","biotype":"protein_coding","ncbi_id":"3225","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. [provided by RefSeq, Jul 2008]","start":53994895,"end":54003337,"strand":1,"description":"homeobox C9 [Source:HGNC Symbol;Acc:HGNC:5130]"}, {"versioned_ensembl_gene_id":"ENSG00000124225.15","gene_symbol":"PMEPA1","gene_name":"prostate transmembrane protein, androgen induced 1 [Source:HGNC Symbol;Acc:HGNC:14107]","synonyms":"TMEPAI,STAG1","biotype":"protein_coding","ncbi_id":"56937","summary":"This gene encodes a transmembrane protein that contains a Smad interacting motif (SIM). Expression of this gene is induced by androgens and transforming growth factor beta, and the encoded protein suppresses the androgen receptor and transforming growth factor beta signaling pathways though interactions with Smad proteins. Overexpression of this gene may play a role in multiple types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":57648392,"end":57711536,"strand":-1,"description":"prostate transmembrane protein, androgen induced 1 [Source:HGNC Symbol;Acc:HGNC:14107]"}, {"versioned_ensembl_gene_id":"ENSG00000011201.11","gene_symbol":"ANOS1","gene_name":"anosmin 1 [Source:HGNC Symbol;Acc:HGNC:6211]","synonyms":"WFDC19,KALIG-1,KAL1,KAL,ADMLX","biotype":"protein_coding","ncbi_id":"3730","summary":"Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]","start":8528874,"end":8732186,"strand":-1,"description":"anosmin 1 [Source:HGNC Symbol;Acc:HGNC:6211]"}, {"versioned_ensembl_gene_id":"ENSG00000164175.14","gene_symbol":"SLC45A2","gene_name":"solute carrier family 45 member 2 [Source:HGNC Symbol;Acc:HGNC:16472]","synonyms":"MATP,AIM-1,OCA4","biotype":"protein_coding","ncbi_id":"51151","summary":"This gene encodes a transporter protein that mediates melanin synthesis. The protein is expressed in a high percentage of melanoma cell lines. Mutations in this gene are a cause of oculocutaneous albinism type 4, and polymorphisms in this gene are associated with variations in skin and hair color. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":33944616,"end":33984730,"strand":-1,"description":"solute carrier family 45 member 2 [Source:HGNC Symbol;Acc:HGNC:16472]"}, {"versioned_ensembl_gene_id":"ENSG00000273049.1","gene_symbol":"AC012531.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53985845,"end":54034888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000037965.5","gene_symbol":"HOXC8","gene_name":"homeobox C8 [Source:HGNC Symbol;Acc:HGNC:5129]","synonyms":"HOX3A,HOX3","biotype":"protein_coding","ncbi_id":"3224","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the regulation of cartilage differentiation. It could also be involved in chondrodysplasias or other cartilage disorders. [provided by RefSeq, Jul 2008]","start":54009106,"end":54012362,"strand":1,"description":"homeobox C8 [Source:HGNC Symbol;Acc:HGNC:5129]"}, {"versioned_ensembl_gene_id":"ENSG00000260252.1","gene_symbol":"AC009087.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72084857,"end":72087443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118557.15","gene_symbol":"PMFBP1","gene_name":"polyamine modulated factor 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17728]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83449","summary":null,"start":72112157,"end":72176878,"strand":-1,"description":"polyamine modulated factor 1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:17728]"}, {"versioned_ensembl_gene_id":"ENSG00000267404.1","gene_symbol":"AC023043.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36273574,"end":36274599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250696.5","gene_symbol":"AC111000.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69182100,"end":69216766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197757.7","gene_symbol":"HOXC6","gene_name":"homeobox C6 [Source:HGNC Symbol;Acc:HGNC:5128]","synonyms":"HOX3,HOX3C","biotype":"protein_coding","ncbi_id":"3223","summary":"This gene belongs to the homeobox family, members of which encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene, HOXC6, is one of several HOXC genes located in a cluster on chromosome 12. Three genes, HOXC5, HOXC4 and HOXC6, share a 5' non-coding exon. Transcripts may include the shared exon spliced to the gene-specific exons, or they may include only the gene-specific exons. Alternatively spliced transcript variants encoding different isoforms have been identified for HOXC6. Transcript variant two includes the shared exon, and transcript variant one includes only gene-specific exons. [provided by RefSeq, Jul 2008]","start":53990624,"end":54030823,"strand":1,"description":"homeobox C6 [Source:HGNC Symbol;Acc:HGNC:5128]"}, {"versioned_ensembl_gene_id":"ENSG00000186812.12","gene_symbol":"ZNF397","gene_name":"zinc finger protein 397 [Source:HGNC Symbol;Acc:HGNC:18818]","synonyms":"ZSCAN15,ZNF47,MGC13250","biotype":"protein_coding","ncbi_id":"84307","summary":"This gene encodes a protein with a N-terminal SCAN domain, and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain. The protein localizes to centromeres during interphase and early prophase, and different isoforms can repress or activate transcription in transfection studies. Multiple transcript variants encoding different isoforms have been found for this gene. Additional variants have been described, but their biological validity has not been determined. [provided by RefSeq, Oct 2009]","start":35241030,"end":35267133,"strand":1,"description":"zinc finger protein 397 [Source:HGNC Symbol;Acc:HGNC:18818]"}, {"versioned_ensembl_gene_id":"ENSG00000165195.15","gene_symbol":"PIGA","gene_name":"phosphatidylinositol glycan anchor biosynthesis class A [Source:HGNC Symbol;Acc:HGNC:8957]","synonyms":"GPI3","biotype":"protein_coding","ncbi_id":"5277","summary":"This gene encodes a protein required for synthesis of N-acetylglucosaminyl phosphatidylinositol (GlcNAc-PI), the first intermediate in the biosynthetic pathway of GPI anchor. The GPI anchor is a glycolipid found on many blood cells and which serves to anchor proteins to the cell surface. Paroxysmal nocturnal hemoglobinuria, an acquired hematologic disorder, has been shown to result from mutations in this gene. Alternate splice variants have been characterized. A related pseudogene is located on chromosome 12. [provided by RefSeq, Jun 2010]","start":15319451,"end":15335580,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class A [Source:HGNC Symbol;Acc:HGNC:8957]"}, {"versioned_ensembl_gene_id":"ENSG00000236098.1","gene_symbol":"AC097059.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94318479,"end":94324569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276374.1","gene_symbol":"AL451142.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88180669,"end":88181409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278688.1","gene_symbol":"AC215799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88187735,"end":88190202,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224296.3","gene_symbol":"MRPL49P1","gene_name":"mitochondrial ribosomal protein L49 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29717]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359748","summary":null,"start":64674853,"end":64675387,"strand":1,"description":"mitochondrial ribosomal protein L49 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29717]"}, {"versioned_ensembl_gene_id":"ENSG00000262304.2","gene_symbol":"AC027796.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3585149,"end":3636249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000058262.9","gene_symbol":"SEC61A1","gene_name":"Sec61 translocon alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:18276]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29927","summary":"The protein encoded by this gene belongs to the SECY/SEC61- alpha family. It appears to play a crucial role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum. This protein found to be tightly associated with membrane-bound ribosomes, either directly or through adaptor proteins. This gene encodes an alpha subunit of the heteromeric SEC61 complex, which also contains beta and gamma subunits. [provided by RefSeq, Jul 2008]","start":128051641,"end":128071683,"strand":1,"description":"Sec61 translocon alpha 1 subunit [Source:HGNC Symbol;Acc:HGNC:18276]"}, {"versioned_ensembl_gene_id":"ENSG00000227436.1","gene_symbol":"FCF1P1","gene_name":"FCF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44613]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422533","summary":null,"start":23619333,"end":23622826,"strand":1,"description":"FCF1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44613]"}, {"versioned_ensembl_gene_id":"ENSG00000261916.1","gene_symbol":"AC027796.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3601761,"end":3602272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262248.1","gene_symbol":"AC027796.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3619256,"end":3619913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197417.7","gene_symbol":"SHPK","gene_name":"sedoheptulokinase [Source:HGNC Symbol;Acc:HGNC:1492]","synonyms":"SHK,CARKL","biotype":"protein_coding","ncbi_id":"23729","summary":"The protein encoded by this gene has weak homology to several carbohydrate kinases, a class of proteins involved in the phosphorylation of sugars as they enter a cell, inhibiting return across the cell membrane. Sequence variation between this novel gene and known carbohydrate kinases suggests the possibility of a different substrate, cofactor or changes in kinetic properties distinguishing it from other carbohydrate kinases. The gene resides in a region commonly deleted in cystinosis patients, suggesting a role as a modifier for the cystinosis phenotype. The genomic region is also rich in Alu repetitive sequences, frequently involved in chromosomal rearrangements. [provided by RefSeq, Jul 2008]","start":3608262,"end":3636322,"strand":-1,"description":"sedoheptulokinase [Source:HGNC Symbol;Acc:HGNC:1492]"}, {"versioned_ensembl_gene_id":"ENSG00000219280.1","gene_symbol":"VN1R8P","gene_name":"vomeronasal 1 receptor 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8497]","synonyms":"ORLP2","biotype":"processed_pseudogene","ncbi_id":"54041","summary":null,"start":13476371,"end":13477263,"strand":1,"description":"vomeronasal 1 receptor 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8497]"}, {"versioned_ensembl_gene_id":"ENSG00000226930.1","gene_symbol":"GTF2IP2","gene_name":"general transcription factor IIi pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16082]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"338448","summary":null,"start":13443373,"end":13489176,"strand":-1,"description":"general transcription factor IIi pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16082]"}, {"versioned_ensembl_gene_id":"ENSG00000204613.10","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30151945,"end":30160934,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000224046.1","gene_symbol":"AC005076.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87151423,"end":87152420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273046.1","gene_symbol":"AC012531.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54017110,"end":54035361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161939.19","gene_symbol":"RNASEK-C17orf49","gene_name":"RNASEK-C17orf49 readthrough [Source:HGNC Symbol;Acc:HGNC:44419]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529209","summary":"This locus represents naturally occurring read-through transcription between the neighboring RNASEK (ribonuclease, RNase K) and C17orf49 (chromosome 17 open reading frame 49) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD) and is unlikely to produce a protein product. [provided by RefSeq, Jan 2011]","start":7012635,"end":7017520,"strand":1,"description":"RNASEK-C17orf49 readthrough [Source:HGNC Symbol;Acc:HGNC:44419]"}, {"versioned_ensembl_gene_id":"ENSG00000135185.11","gene_symbol":"TMEM243","gene_name":"transmembrane protein 243 [Source:HGNC Symbol;Acc:HGNC:21707]","synonyms":"MM-TRAG,MGC4175,C7orf23","biotype":"protein_coding","ncbi_id":"79161","summary":null,"start":87196160,"end":87220587,"strand":-1,"description":"transmembrane protein 243 [Source:HGNC Symbol;Acc:HGNC:21707]"}, {"versioned_ensembl_gene_id":"ENSG00000179938.12","gene_symbol":"GOLGA8J","gene_name":"golgin A8 family member J [Source:HGNC Symbol;Acc:HGNC:38650]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653073","summary":null,"start":30083053,"end":30093499,"strand":1,"description":"golgin A8 family member J [Source:HGNC Symbol;Acc:HGNC:38650]"}, {"versioned_ensembl_gene_id":"ENSG00000260597.1","gene_symbol":"AC012531.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54019910,"end":54022589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263338.1","gene_symbol":"AC027796.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3577955,"end":3578853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257121.1","gene_symbol":"AC126615.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95100531,"end":95101045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251151.2","gene_symbol":"HOXC-AS3","gene_name":"HOXC cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:43751]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874365","summary":null,"start":53981509,"end":53985519,"strand":-1,"description":"HOXC cluster antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:43751]"}, {"versioned_ensembl_gene_id":"ENSG00000174628.16","gene_symbol":"IQCK","gene_name":"IQ motif containing K [Source:HGNC Symbol;Acc:HGNC:28556]","synonyms":"MGC35048,FLJ36575","biotype":"protein_coding","ncbi_id":"124152","summary":"This gene belongs to the IQ motif-containing family of proteins. The IQ motif serves as a binding site for different EF-hand proteins such as calmodulin. This gene was identified as a potential candidate gene for obsessive-compulsive disorder in a genome-wide association study. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":19716456,"end":19858467,"strand":1,"description":"IQ motif containing K [Source:HGNC Symbol;Acc:HGNC:28556]"}, {"versioned_ensembl_gene_id":"ENSG00000241905.1","gene_symbol":"NDUFS6P1","gene_name":"NADH:ubiquinone oxidoreductase subunit S6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075209","summary":null,"start":135959275,"end":135959590,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit S6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52274]"}, {"versioned_ensembl_gene_id":"ENSG00000250451.5","gene_symbol":"HOXC-AS1","gene_name":"HOXC cluster antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43749]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874363","summary":null,"start":53999022,"end":54000010,"strand":-1,"description":"HOXC cluster antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43749]"}, {"versioned_ensembl_gene_id":"ENSG00000196689.11","gene_symbol":"TRPV1","gene_name":"transient receptor potential cation channel subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:12716]","synonyms":"VR1","biotype":"protein_coding","ncbi_id":"7442","summary":"Capsaicin, the main pungent ingredient in hot chili peppers, elicits a sensation of burning pain by selectively activating sensory neurons that convey information about noxious stimuli to the central nervous system. The protein encoded by this gene is a receptor for capsaicin and is a non-selective cation channel that is structurally related to members of the TRP family of ion channels. This receptor is also activated by increases in temperature in the noxious range, suggesting that it functions as a transducer of painful thermal stimuli in vivo. Four transcript variants encoding the same protein, but with different 5' UTR sequence, have been described for this gene. [provided by RefSeq, Jul 2008]","start":3565444,"end":3609411,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:12716]"}, {"versioned_ensembl_gene_id":"ENSG00000250133.2","gene_symbol":"HOXC-AS2","gene_name":"HOXC cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43750]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874364","summary":null,"start":53993810,"end":53996785,"strand":-1,"description":"HOXC cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43750]"}, {"versioned_ensembl_gene_id":"ENSG00000250914.1","gene_symbol":"AC139783.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33970863,"end":33972628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259468.1","gene_symbol":"AC079203.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34255286,"end":34257832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206500.9","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"LIRF,HZFw1","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30059837,"end":30065413,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000226331.1","gene_symbol":"RPL23AP28","gene_name":"ribosomal protein L23a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36727]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271457","summary":null,"start":222044525,"end":222044994,"strand":-1,"description":"ribosomal protein L23a pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36727]"}, {"versioned_ensembl_gene_id":"ENSG00000198353.7","gene_symbol":"HOXC4","gene_name":"homeobox C4 [Source:HGNC Symbol;Acc:HGNC:5126]","synonyms":"HOX3E,HOX3","biotype":"protein_coding","ncbi_id":"3221","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene, HOXC4, is one of several homeobox HOXC genes located in a cluster on chromosome 12. Three genes, HOXC5, HOXC4 and HOXC6, share a 5' non-coding exon. Transcripts may include the shared exon spliced to the gene-specific exons, or they may include only the gene-specific exons. Two alternatively spliced variants that encode the same protein have been described for HOXC4. Transcript variant one includes the shared exon, and transcript variant two includes only gene-specific exons. [provided by RefSeq, Jul 2008]","start":54016931,"end":54056030,"strand":1,"description":"homeobox C4 [Source:HGNC Symbol;Acc:HGNC:5126]"}, {"versioned_ensembl_gene_id":"ENSG00000140199.11","gene_symbol":"SLC12A6","gene_name":"solute carrier family 12 member 6 [Source:HGNC Symbol;Acc:HGNC:10914]","synonyms":"KCC3,ACCPN","biotype":"protein_coding","ncbi_id":"9990","summary":"This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy. [provided by RefSeq, Jul 2008]","start":34229996,"end":34338060,"strand":-1,"description":"solute carrier family 12 member 6 [Source:HGNC Symbol;Acc:HGNC:10914]"}, {"versioned_ensembl_gene_id":"ENSG00000260108.1","gene_symbol":"AC026464.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":69463844,"end":69466264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206501.8","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"CFAP255,HCGV,Tctex5,HCG-V,TCTE5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30056276,"end":30059900,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000229950.1","gene_symbol":"TFAP2A-AS1","gene_name":"TFAP2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40579]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100130275","summary":null,"start":10409340,"end":10416446,"strand":1,"description":"TFAP2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40579]"}, {"versioned_ensembl_gene_id":"ENSG00000180818.4","gene_symbol":"HOXC10","gene_name":"homeobox C10 [Source:HGNC Symbol;Acc:HGNC:5122]","synonyms":"HOX3I","biotype":"protein_coding","ncbi_id":"3226","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The protein level is controlled during cell differentiation and proliferation, which may indicate this protein has a role in origin activation. [provided by RefSeq, Jul 2008]","start":53985065,"end":53990279,"strand":1,"description":"homeobox C10 [Source:HGNC Symbol;Acc:HGNC:5122]"}, {"versioned_ensembl_gene_id":"ENSG00000261527.1","gene_symbol":"AC026464.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69443240,"end":69444290,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275413.1","gene_symbol":"AC002553.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16023323,"end":16023653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103018.16","gene_symbol":"CYB5B","gene_name":"cytochrome b5 type B [Source:HGNC Symbol;Acc:HGNC:24374]","synonyms":"CYB5-M","biotype":"protein_coding","ncbi_id":"80777","summary":null,"start":69424525,"end":69466266,"strand":1,"description":"cytochrome b5 type B [Source:HGNC Symbol;Acc:HGNC:24374]"}, {"versioned_ensembl_gene_id":"ENSG00000166582.9","gene_symbol":"CENPV","gene_name":"centromere protein V [Source:HGNC Symbol;Acc:HGNC:29920]","synonyms":"PRR6,p30,CENP-V","biotype":"protein_coding","ncbi_id":"201161","summary":null,"start":16342534,"end":16353656,"strand":-1,"description":"centromere protein V [Source:HGNC Symbol;Acc:HGNC:29920]"}, {"versioned_ensembl_gene_id":"ENSG00000223611.5","gene_symbol":"SUPT20HL2","gene_name":"SUPT20H like 2 [Source:HGNC Symbol;Acc:HGNC:31797]","synonyms":"FAM48B2","biotype":"processed_pseudogene","ncbi_id":"170067","summary":null,"start":24310907,"end":24313315,"strand":-1,"description":"SUPT20H like 2 [Source:HGNC Symbol;Acc:HGNC:31797]"}, {"versioned_ensembl_gene_id":"ENSG00000138686.9","gene_symbol":"BBS7","gene_name":"Bardet-Biedl syndrome 7 [Source:HGNC Symbol;Acc:HGNC:18758]","synonyms":"FLJ10715,BBS2L1","biotype":"protein_coding","ncbi_id":"55212","summary":"This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy; however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014]","start":121824440,"end":121870497,"strand":-1,"description":"Bardet-Biedl syndrome 7 [Source:HGNC Symbol;Acc:HGNC:18758]"}, {"versioned_ensembl_gene_id":"ENSG00000228184.1","gene_symbol":"SNX19P1","gene_name":"sorting nexin 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16765]","synonyms":"SNX19P","biotype":"processed_pseudogene","ncbi_id":"378810","summary":null,"start":13525599,"end":13528579,"strand":1,"description":"sorting nexin 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16765]"}, {"versioned_ensembl_gene_id":"ENSG00000268573.1","gene_symbol":"AC011815.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35280867,"end":35290201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137203.10","gene_symbol":"TFAP2A","gene_name":"transcription factor AP-2 alpha [Source:HGNC Symbol;Acc:HGNC:11742]","synonyms":"TFAP2,AP2TF,AP-2","biotype":"protein_coding","ncbi_id":"7020","summary":"The protein encoded by this gene is a transcription factor that binds the consensus sequence 5'-GCCNNNGGC-3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS). Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]","start":10393186,"end":10419659,"strand":-1,"description":"transcription factor AP-2 alpha [Source:HGNC Symbol;Acc:HGNC:11742]"}, {"versioned_ensembl_gene_id":"ENSG00000279989.1","gene_symbol":"AC011815.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35257040,"end":35257512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186814.13","gene_symbol":"ZSCAN30","gene_name":"zinc finger and SCAN domain containing 30 [Source:HGNC Symbol;Acc:HGNC:33517]","synonyms":"ZNF917,ZNF397OS","biotype":"protein_coding","ncbi_id":"100101467","summary":null,"start":35251058,"end":35290245,"strand":-1,"description":"zinc finger and SCAN domain containing 30 [Source:HGNC Symbol;Acc:HGNC:33517]"}, {"versioned_ensembl_gene_id":"ENSG00000278709.1","gene_symbol":"NKILA","gene_name":"NF-kappaB interacting lncRNA [Source:HGNC Symbol;Acc:HGNC:51599]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105416157","summary":null,"start":57710183,"end":57712780,"strand":1,"description":"NF-kappaB interacting lncRNA [Source:HGNC Symbol;Acc:HGNC:51599]"}, {"versioned_ensembl_gene_id":"ENSG00000101558.13","gene_symbol":"VAPA","gene_name":"VAMP associated protein A [Source:HGNC Symbol;Acc:HGNC:12648]","synonyms":"VAP-A,hVAP-33","biotype":"protein_coding","ncbi_id":"9218","summary":"The protein encoded by this gene is a type IV membrane protein. It is present in the plasma membrane and intracellular vesicles. It may also be associated with the cytoskeleton. This protein may function in vesicle trafficking, membrane fusion, protein complex assembly and cell motility. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":9914002,"end":9960021,"strand":1,"description":"VAMP associated protein A [Source:HGNC Symbol;Acc:HGNC:12648]"}, {"versioned_ensembl_gene_id":"ENSG00000228689.7","gene_symbol":"AL355997.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51599723,"end":51622884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243855.1","gene_symbol":"RPL12P5","gene_name":"ribosomal protein L12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19669]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"319142","summary":null,"start":30791098,"end":30791489,"strand":1,"description":"ribosomal protein L12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19669]"}, {"versioned_ensembl_gene_id":"ENSG00000135164.18","gene_symbol":"DMTF1","gene_name":"cyclin D binding myb like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:14603]","synonyms":"MRUL,hDMP1,DMTF,DMP1","biotype":"protein_coding","ncbi_id":"9988","summary":"This gene encodes a transcription factor that contains a cyclin D-binding domain, three central Myb-like repeats, and two flanking acidic transactivation domains at the N- and C-termini. The encoded protein is induced by the oncogenic Ras signaling pathway and functions as a tumor suppressor by activating the transcription of ARF and thus the ARF-p53 pathway to arrest cell growth or induce apoptosis. It also activates the transcription of aminopeptidase N and may play a role in hematopoietic cell differentiation. The transcriptional activity of this protein is regulated by binding of D-cyclins. This gene is hemizygously deleted in approximately 40% of human non-small-cell lung cancer and is a potential prognostic and gene-therapy target for non-small-cell lung cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":87152361,"end":87196337,"strand":1,"description":"cyclin D binding myb like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:14603]"}, {"versioned_ensembl_gene_id":"ENSG00000213867.4","gene_symbol":"AL049830.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30821419,"end":30821843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253237.2","gene_symbol":"AC034114.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80351132,"end":80351416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267532.5","gene_symbol":"MIR497HG","gene_name":"mir-497-195 cluster host gene [Source:HGNC Symbol;Acc:HGNC:39523]","synonyms":"MIR195HG","biotype":"antisense_RNA","ncbi_id":"100506755","summary":null,"start":7015818,"end":7019659,"strand":-1,"description":"mir-497-195 cluster host gene [Source:HGNC Symbol;Acc:HGNC:39523]"}, {"versioned_ensembl_gene_id":"ENSG00000258648.1","gene_symbol":"UBE2CP1","gene_name":"ubiquitin conjugating enzyme E2 C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19670]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326105","summary":null,"start":30683045,"end":30683598,"strand":-1,"description":"ubiquitin conjugating enzyme E2 C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19670]"}, {"versioned_ensembl_gene_id":"ENSG00000258558.1","gene_symbol":"AL121852.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30734926,"end":30822702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240513.1","gene_symbol":"AL049830.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30819714,"end":30819914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274209.4","gene_symbol":"ANTXRL","gene_name":"anthrax toxin receptor like [Source:HGNC Symbol;Acc:HGNC:27277]","synonyms":null,"biotype":"protein_coding","ncbi_id":"195977","summary":null,"start":46286345,"end":46330207,"strand":1,"description":"anthrax toxin receptor like [Source:HGNC Symbol;Acc:HGNC:27277]"}, {"versioned_ensembl_gene_id":"ENSG00000174839.12","gene_symbol":"DENND6A","gene_name":"DENN domain containing 6A [Source:HGNC Symbol;Acc:HGNC:26635]","synonyms":"FLJ34969,FAM116A,AFI1A","biotype":"protein_coding","ncbi_id":"201627","summary":null,"start":57625457,"end":57693089,"strand":-1,"description":"DENN domain containing 6A [Source:HGNC Symbol;Acc:HGNC:26635]"}, {"versioned_ensembl_gene_id":"ENSG00000185252.18","gene_symbol":"ZNF74","gene_name":"zinc finger protein 74 [Source:HGNC Symbol;Acc:HGNC:13144]","synonyms":"ZNF520,Zfp520,Cos52","biotype":"protein_coding","ncbi_id":"7625","summary":null,"start":20394115,"end":20408461,"strand":1,"description":"zinc finger protein 74 [Source:HGNC Symbol;Acc:HGNC:13144]"}, {"versioned_ensembl_gene_id":"ENSG00000282008.1","gene_symbol":"GAPDHP26","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37778]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392374","summary":null,"start":100975668,"end":100976682,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37778]"}, {"versioned_ensembl_gene_id":"ENSG00000043093.13","gene_symbol":"DCUN1D1","gene_name":"defective in cullin neddylation 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18184]","synonyms":"Tes3,SCRO,SCCRO,RP42,DCUN1L1","biotype":"protein_coding","ncbi_id":"54165","summary":null,"start":182938074,"end":182985953,"strand":-1,"description":"defective in cullin neddylation 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18184]"}, {"versioned_ensembl_gene_id":"ENSG00000262943.7","gene_symbol":"ALOX12P2","gene_name":"arachidonate 12-lipoxygenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:432]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"245","summary":null,"start":6853861,"end":6954107,"strand":1,"description":"arachidonate 12-lipoxygenase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:432]"}, {"versioned_ensembl_gene_id":"ENSG00000251867.3","gene_symbol":"AC009812.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80484561,"end":80485619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205189.11","gene_symbol":"ZBTB10","gene_name":"zinc finger and BTB domain containing 10 [Source:HGNC Symbol;Acc:HGNC:30953]","synonyms":"RINZF,FLJ12752","biotype":"protein_coding","ncbi_id":"65986","summary":null,"start":80485619,"end":80526265,"strand":1,"description":"zinc finger and BTB domain containing 10 [Source:HGNC Symbol;Acc:HGNC:30953]"}, {"versioned_ensembl_gene_id":"ENSG00000092108.20","gene_symbol":"SCFD1","gene_name":"sec1 family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20726]","synonyms":"C14orf163,STXBP1L2,SLY1,RA410,KIAA0917","biotype":"protein_coding","ncbi_id":"23256","summary":null,"start":30622112,"end":30735812,"strand":1,"description":"sec1 family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20726]"}, {"versioned_ensembl_gene_id":"ENSG00000101367.8","gene_symbol":"MAPRE1","gene_name":"microtubule associated protein RP/EB family member 1 [Source:HGNC Symbol;Acc:HGNC:6890]","synonyms":"EB1","biotype":"protein_coding","ncbi_id":"22919","summary":"The protein encoded by this gene was first identified by its binding to the APC protein which is often mutated in familial and sporadic forms of colorectal cancer. This protein localizes to microtubules, especially the growing ends, in interphase cells. During mitosis, the protein is associated with the centrosomes and spindle microtubules. The protein also associates with components of the dynactin complex and the intermediate chain of cytoplasmic dynein. Because of these associations, it is thought that this protein is involved in the regulation of microtubule structures and chromosome stability. This gene is a member of the RP/EB family. [provided by RefSeq, Jul 2008]","start":32819893,"end":32850405,"strand":1,"description":"microtubule associated protein RP/EB family member 1 [Source:HGNC Symbol;Acc:HGNC:6890]"}, {"versioned_ensembl_gene_id":"ENSG00000234087.1","gene_symbol":"AL356299.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34347671,"end":34347785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165215.6","gene_symbol":"CLDN3","gene_name":"claudin 3 [Source:HGNC Symbol;Acc:HGNC:2045]","synonyms":"RVP1,HRVP1,CPETR2,CPE-R2,C7orf1","biotype":"protein_coding","ncbi_id":"1365","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this intronless gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is also a low-affinity receptor for Clostridium perfringens enterotoxin, and shares aa sequence similarity with a putative apoptosis-related protein found in rat. [provided by RefSeq, Jul 2008]","start":73768997,"end":73770270,"strand":-1,"description":"claudin 3 [Source:HGNC Symbol;Acc:HGNC:2045]"}, {"versioned_ensembl_gene_id":"ENSG00000176953.12","gene_symbol":"NFATC2IP","gene_name":"nuclear factor of activated T-cells 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:25906]","synonyms":"RAD60,NIP45,FLJ14639,ESC2","biotype":"protein_coding","ncbi_id":"84901","summary":null,"start":28950807,"end":28967097,"strand":1,"description":"nuclear factor of activated T-cells 2 interacting protein [Source:HGNC Symbol;Acc:HGNC:25906]"}, {"versioned_ensembl_gene_id":"ENSG00000189143.9","gene_symbol":"CLDN4","gene_name":"claudin 4 [Source:HGNC Symbol;Acc:HGNC:2046]","synonyms":"WBSCR8,hCPE-R,CPETR1,CPETR,CPE-R","biotype":"protein_coding","ncbi_id":"1364","summary":"The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. [provided by RefSeq, Sep 2013]","start":73799542,"end":73832693,"strand":1,"description":"claudin 4 [Source:HGNC Symbol;Acc:HGNC:2046]"}, {"versioned_ensembl_gene_id":"ENSG00000261312.1","gene_symbol":"AC002550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19706351,"end":19715383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260536.1","gene_symbol":"AL035071.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32843128,"end":32854257,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261939.1","gene_symbol":"LARP7P2","gene_name":"La ribonucleoprotein domain family member 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49764]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481699","summary":null,"start":19819504,"end":19819628,"strand":-1,"description":"La ribonucleoprotein domain family member 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49764]"}, {"versioned_ensembl_gene_id":"ENSG00000261195.1","gene_symbol":"AC027130.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19761172,"end":19766099,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243686.2","gene_symbol":"AC002553.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16044621,"end":16044961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283043.1","gene_symbol":"AC097655.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60038269,"end":60038586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122435.9","gene_symbol":"TRMT13","gene_name":"tRNA methyltransferase 13 homolog [Source:HGNC Symbol;Acc:HGNC:25502]","synonyms":"FLJ11219,FLJ10287,CCDC76","biotype":"protein_coding","ncbi_id":"54482","summary":null,"start":100133150,"end":100150497,"strand":1,"description":"tRNA methyltransferase 13 homolog [Source:HGNC Symbol;Acc:HGNC:25502]"}, {"versioned_ensembl_gene_id":"ENSG00000250447.5","gene_symbol":"LINC02105","gene_name":"long intergenic non-protein coding RNA 2105 [Source:HGNC Symbol;Acc:HGNC:52960]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378966","summary":null,"start":53776644,"end":53819686,"strand":-1,"description":"long intergenic non-protein coding RNA 2105 [Source:HGNC Symbol;Acc:HGNC:52960]"}, {"versioned_ensembl_gene_id":"ENSG00000271461.1","gene_symbol":"AL109809.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1756756,"end":1758940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276571.1","gene_symbol":"AC002550.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19694035,"end":19694428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274184.1","gene_symbol":"AC011815.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35268218,"end":35270238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244461.1","gene_symbol":"LINC02077","gene_name":"long intergenic non-protein coding RNA 2077 [Source:HGNC Symbol;Acc:HGNC:52925]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377172","summary":null,"start":78038705,"end":78046794,"strand":-1,"description":"long intergenic non-protein coding RNA 2077 [Source:HGNC Symbol;Acc:HGNC:52925]"}, {"versioned_ensembl_gene_id":"ENSG00000182816.8","gene_symbol":"KRTAP13-2","gene_name":"keratin associated protein 13-2 [Source:HGNC Symbol;Acc:HGNC:18923]","synonyms":"KAP13-2","biotype":"protein_coding","ncbi_id":"337959","summary":null,"start":30371391,"end":30372257,"strand":-1,"description":"keratin associated protein 13-2 [Source:HGNC Symbol;Acc:HGNC:18923]"}, {"versioned_ensembl_gene_id":"ENSG00000103544.14","gene_symbol":"C16orf62","gene_name":"chromosome 16 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:24641]","synonyms":"MGC16824","biotype":"protein_coding","ncbi_id":"57020","summary":null,"start":19555240,"end":19706793,"strand":1,"description":"chromosome 16 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:24641]"}, {"versioned_ensembl_gene_id":"ENSG00000280744.1","gene_symbol":"LINC01173","gene_name":"long intergenic non-protein coding RNA 1173 [Source:NCBI gene;Acc:106144537]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144537","summary":null,"start":234682668,"end":234717764,"strand":1,"description":"long intergenic non-protein coding RNA 1173 [Source:NCBI gene;Acc:106144537]"}, {"versioned_ensembl_gene_id":"ENSG00000204934.10","gene_symbol":"ATP6V0E2-AS1","gene_name":"ATP6V0E2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44180]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"401431","summary":null,"start":149867697,"end":149880610,"strand":-1,"description":"ATP6V0E2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44180]"}, {"versioned_ensembl_gene_id":"ENSG00000231418.1","gene_symbol":"AC005090.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31414645,"end":31421286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249066.1","gene_symbol":"LINC02496","gene_name":"long intergenic non-protein coding RNA 2496 [Source:HGNC Symbol;Acc:HGNC:53480]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377248","summary":null,"start":60750586,"end":60789999,"strand":1,"description":"long intergenic non-protein coding RNA 2496 [Source:HGNC Symbol;Acc:HGNC:53480]"}, {"versioned_ensembl_gene_id":"ENSG00000217791.4","gene_symbol":"ASS1P9","gene_name":"argininosuccinate synthetase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:772]","synonyms":"ASSP9","biotype":"processed_pseudogene","ncbi_id":"454","summary":null,"start":53859166,"end":53860401,"strand":1,"description":"argininosuccinate synthetase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:772]"}, {"versioned_ensembl_gene_id":"ENSG00000248237.2","gene_symbol":"AC105420.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60784115,"end":60784696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278593.1","gene_symbol":"AC104394.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":234743542,"end":234745606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042493.15","gene_symbol":"CAPG","gene_name":"capping actin protein, gelsolin like [Source:HGNC Symbol;Acc:HGNC:1474]","synonyms":"MCP,AFCP","biotype":"protein_coding","ncbi_id":"822","summary":"This gene encodes a member of the gelsolin/villin family of actin-regulatory proteins. The encoded protein reversibly blocks the barbed ends of F-actin filaments in a Ca2+ and phosphoinositide-regulated manner, but does not sever preformed actin filaments. By capping the barbed ends of actin filaments, the encoded protein contributes to the control of actin-based motility in non-muscle cells. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2012]","start":85394748,"end":85418432,"strand":-1,"description":"capping actin protein, gelsolin like [Source:HGNC Symbol;Acc:HGNC:1474]"}, {"versioned_ensembl_gene_id":"ENSG00000272416.1","gene_symbol":"AC025175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53880293,"end":53881051,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269220.1","gene_symbol":"LINC00528","gene_name":"long intergenic non-protein coding RNA 528 [Source:HGNC Symbol;Acc:HGNC:26875]","synonyms":"FLJ40542,C22orf37","biotype":"lincRNA","ncbi_id":"200298","summary":null,"start":17777322,"end":17779481,"strand":1,"description":"long intergenic non-protein coding RNA 528 [Source:HGNC Symbol;Acc:HGNC:26875]"}, {"versioned_ensembl_gene_id":"ENSG00000232528.3","gene_symbol":"AL109809.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":1767957,"end":1779995,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171130.17","gene_symbol":"ATP6V0E2","gene_name":"ATPase H+ transporting V0 subunit e2 [Source:HGNC Symbol;Acc:HGNC:21723]","synonyms":"C7orf32,ATP6V0E2L","biotype":"protein_coding","ncbi_id":"155066","summary":"Multisubunit vacuolar-type proton pumps, or H(+)-ATPases, acidify various intracellular compartments, such as vacuoles, clathrin-coated and synaptic vesicles, endosomes, lysosomes, and chromaffin granules. H(+)-ATPases are also found in plasma membranes of specialized cells, where they play roles in urinary acidification, bone resorption, and sperm maturation. Multiple subunits form H(+)-ATPases, with proteins of the V1 class hydrolyzing ATP for energy to transport H+, and proteins of the V0 class forming an integral membrane domain through which H+ is transported. ATP6V0E2 encodes an isoform of the H(+)-ATPase V0 e subunit, an essential proton pump component (Blake-Palmer et al., 2007 [PubMed 17350184]).[supplied by OMIM, Mar 2008]","start":149872968,"end":149880698,"strand":1,"description":"ATPase H+ transporting V0 subunit e2 [Source:HGNC Symbol;Acc:HGNC:21723]"}, {"versioned_ensembl_gene_id":"ENSG00000081913.13","gene_symbol":"PHLPP1","gene_name":"PH domain and leucine rich repeat protein phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:20610]","synonyms":"SCOP,PPM3A,PLEKHE1,PHLPP,KIAA0606","biotype":"protein_coding","ncbi_id":"23239","summary":"This gene encodes a member of the serine/threonine phosphatase family. The encoded protein promotes apoptosis by dephosphorylating and inactivating the serine/threonine kinase Akt, and functions as a tumor suppressor in multiple types of cancer. Increased expression of this gene may also play a role in obesity and type 2 diabetes by interfering with Akt-mediated insulin signaling. [provided by RefSeq, Dec 2011]","start":62715450,"end":62980433,"strand":1,"description":"PH domain and leucine rich repeat protein phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:20610]"}, {"versioned_ensembl_gene_id":"ENSG00000143333.6","gene_symbol":"RGS16","gene_name":"regulator of G protein signaling 16 [Source:HGNC Symbol;Acc:HGNC:9997]","synonyms":"RGS-r,A28-RGS14","biotype":"protein_coding","ncbi_id":"6004","summary":"The protein encoded by this gene belongs to the 'regulator of G protein signaling' family. It inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits. It also may play a role in regulating the kinetics of signaling in the phototransduction cascade. [provided by RefSeq, Jul 2008]","start":182598623,"end":182604408,"strand":-1,"description":"regulator of G protein signaling 16 [Source:HGNC Symbol;Acc:HGNC:9997]"}, {"versioned_ensembl_gene_id":"ENSG00000125538.11","gene_symbol":"IL1B","gene_name":"interleukin 1 beta [Source:HGNC Symbol;Acc:HGNC:5992]","synonyms":"IL1F2,IL1-BETA,IL-1B","biotype":"protein_coding","ncbi_id":"3553","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine is produced by activated macrophages as a proprotein, which is proteolytically processed to its active form by caspase 1 (CASP1/ICE). This cytokine is an important mediator of the inflammatory response, and is involved in a variety of cellular activities, including cell proliferation, differentiation, and apoptosis. The induction of cyclooxygenase-2 (PTGS2/COX2) by this cytokine in the central nervous system (CNS) is found to contribute to inflammatory pain hypersensitivity. Similarly, IL-1B has been implicated in human osteoarthritis pathogenesis. Patients with severe Coronavirus Disease 2019 (COVID-19) present elevated levels of pro-inflammatory cytokines such as IL-1B in bronchial alveolar lavage fluid samples. The lung damage induced by the Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is to a large extent, a result of the inflammatory response promoted by cytokines such as IL-1B. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. [provided by RefSeq, Jul 2020]","start":112829751,"end":112836903,"strand":-1,"description":"interleukin 1 beta [Source:HGNC Symbol;Acc:HGNC:5992]"}, {"versioned_ensembl_gene_id":"ENSG00000172789.3","gene_symbol":"HOXC5","gene_name":"homeobox C5 [Source:HGNC Symbol;Acc:HGNC:5127]","synonyms":"HOX3D,HOX3","biotype":"protein_coding","ncbi_id":"3222","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene, HOXC5, is one of several homeobox HOXC genes located in a cluster on chromosome 12. Three genes, HOXC5, HOXC4 and HOXC6, share a 5' non-coding exon. Transcripts may include the shared exon spliced to the gene-specific exons, or they may include only the gene-specific exons. Two alternatively spliced variants have been described for HOXC5. The transcript variant which includes the shared exon apparently doesn't encode a protein. The protein-coding transcript variant contains gene-specific exons only. [provided by RefSeq, Jul 2008]","start":54032853,"end":54035358,"strand":1,"description":"homeobox C5 [Source:HGNC Symbol;Acc:HGNC:5127]"}, {"versioned_ensembl_gene_id":"ENSG00000261701.6","gene_symbol":"HPR","gene_name":"haptoglobin-related protein [Source:HGNC Symbol;Acc:HGNC:5156]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3250","summary":"This gene encodes a haptoglobin-related protein that binds hemoglobin as efficiently as haptoglobin. Unlike haptoglobin, plasma concentration of this protein is unaffected in patients with sickle cell anemia and extensive intravascular hemolysis, suggesting a difference in binding between haptoglobin-hemoglobin and haptoglobin-related protein-hemoglobin complexes to CD163, the hemoglobin scavenger receptor. This protein may also be a clinically important predictor of recurrence of breast cancer. [provided by RefSeq, Oct 2011]","start":72063224,"end":72077246,"strand":1,"description":"haptoglobin-related protein [Source:HGNC Symbol;Acc:HGNC:5156]"}, {"versioned_ensembl_gene_id":"ENSG00000227841.1","gene_symbol":"MTND5P31","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42293]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873267","summary":null,"start":201556892,"end":201558265,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42293]"}, {"versioned_ensembl_gene_id":"ENSG00000224590.1","gene_symbol":"MTND3P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52076]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075278","summary":null,"start":201553688,"end":201554031,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52076]"}, {"versioned_ensembl_gene_id":"ENSG00000224210.1","gene_symbol":"TRIM60P5Y","gene_name":"tripartite motif containing 60 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38430]","synonyms":"TRIM60PY5,TRIM60P5","biotype":"processed_pseudogene","ncbi_id":"100420368","summary":null,"start":24494709,"end":24495583,"strand":-1,"description":"tripartite motif containing 60 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38430]"}, {"versioned_ensembl_gene_id":"ENSG00000250375.2","gene_symbol":"AC097501.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59047020,"end":59075256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249889.1","gene_symbol":"ALG1L11P","gene_name":"asparagine-linked glycosylation 1-like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:44380]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480789","summary":null,"start":12178697,"end":12182719,"strand":1,"description":"asparagine-linked glycosylation 1-like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:44380]"}, {"versioned_ensembl_gene_id":"ENSG00000151388.10","gene_symbol":"ADAMTS12","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 12 [Source:HGNC Symbol;Acc:HGNC:14605]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81792","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS-1) motif. Individual members of this family differ in the number of C-terminal TS-1 motifs, and some have unique C-terminal domains. The enzyme encoded by this gene contains eight TS-1 motifs. It may play roles in pulmonary cells during fetal development or in tumor processes through its proteolytic activity or as a molecule potentially involved in regulation of cell adhesion. [provided by RefSeq, Jul 2008]","start":33523535,"end":33892192,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 12 [Source:HGNC Symbol;Acc:HGNC:14605]"}, {"versioned_ensembl_gene_id":"ENSG00000256149.1","gene_symbol":"AC087863.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118849354,"end":118908930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273419.1","gene_symbol":"AC004877.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149858400,"end":149862492,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122574.10","gene_symbol":"WIPF3","gene_name":"WAS/WASL interacting protein family member 3 [Source:HGNC Symbol;Acc:HGNC:22004]","synonyms":"FLJ36931,CR16","biotype":"protein_coding","ncbi_id":"644150","summary":null,"start":29806486,"end":29917066,"strand":1,"description":"WAS/WASL interacting protein family member 3 [Source:HGNC Symbol;Acc:HGNC:22004]"}, {"versioned_ensembl_gene_id":"ENSG00000078237.6","gene_symbol":"TIGAR","gene_name":"TP53 induced glycolysis regulatory phosphatase [Source:HGNC Symbol;Acc:HGNC:1185]","synonyms":"C12orf5","biotype":"protein_coding","ncbi_id":"57103","summary":"This gene is regulated as part of the p53 tumor suppressor pathway and encodes a protein with sequence similarity to the bisphosphate domain of the glycolytic enzyme that degrades fructose-2,6-bisphosphate. The protein functions by blocking glycolysis and directing the pathway into the pentose phosphate shunt. Expression of this protein also protects cells from DNA damaging reactive oxygen species and provides some protection from DNA damage-induced apoptosis. The 12p13.32 region that includes this gene is paralogous to the 11q13.3 region. [provided by RefSeq, Jul 2008]","start":4307763,"end":4354593,"strand":1,"description":"TP53 induced glycolysis regulatory phosphatase [Source:HGNC Symbol;Acc:HGNC:1185]"}, {"versioned_ensembl_gene_id":"ENSG00000213970.3","gene_symbol":"AC006122.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4324372,"end":4324811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283110.1","gene_symbol":"AC141257.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33386105,"end":33386349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164236.11","gene_symbol":"ANKRD33B","gene_name":"ankyrin repeat domain 33B [Source:HGNC Symbol;Acc:HGNC:35240]","synonyms":null,"biotype":"protein_coding","ncbi_id":"651746","summary":null,"start":10564330,"end":10657816,"strand":1,"description":"ankyrin repeat domain 33B [Source:HGNC Symbol;Acc:HGNC:35240]"}, {"versioned_ensembl_gene_id":"ENSG00000167699.13","gene_symbol":"GLOD4","gene_name":"glyoxalase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:14111]","synonyms":"HC71,CGI-150,C17orf25","biotype":"protein_coding","ncbi_id":"51031","summary":null,"start":757097,"end":783390,"strand":-1,"description":"glyoxalase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:14111]"}, {"versioned_ensembl_gene_id":"ENSG00000170191.4","gene_symbol":"NANP","gene_name":"N-acetylneuraminic acid phosphatase [Source:HGNC Symbol;Acc:HGNC:16140]","synonyms":"MGC26833,HDHD4,dJ694B14.3,C20orf147","biotype":"protein_coding","ncbi_id":"140838","summary":null,"start":25612935,"end":25624175,"strand":-1,"description":"N-acetylneuraminic acid phosphatase [Source:HGNC Symbol;Acc:HGNC:16140]"}, {"versioned_ensembl_gene_id":"ENSG00000179826.6","gene_symbol":"MRGPRX3","gene_name":"MAS related GPR family member X3 [Source:HGNC Symbol;Acc:HGNC:17980]","synonyms":"MRGX3","biotype":"protein_coding","ncbi_id":"117195","summary":"This gene encodes a member of the mas-related/sensory neuron specific subfamily of G protein coupled receptors. The encoded protein may be involved in sensory neuron regulation and in the modulation of pain. [provided by RefSeq, Oct 2009]","start":18120955,"end":18138480,"strand":1,"description":"MAS related GPR family member X3 [Source:HGNC Symbol;Acc:HGNC:17980]"}, {"versioned_ensembl_gene_id":"ENSG00000229196.3","gene_symbol":"AC087071.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130141731,"end":130142615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131725.13","gene_symbol":"WDR44","gene_name":"WD repeat domain 44 [Source:HGNC Symbol;Acc:HGNC:30512]","synonyms":"RPH11,RAB11BP,DKFZp686L20145","biotype":"protein_coding","ncbi_id":"54521","summary":"This gene encodes a protein that interacts with the small GTPase rab11. A similar protein in rat binds the GTP-containing active form of rab11. This protein may play a role in endosome recycling. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":118346073,"end":118449961,"strand":1,"description":"WD repeat domain 44 [Source:HGNC Symbol;Acc:HGNC:30512]"}, {"versioned_ensembl_gene_id":"ENSG00000163517.14","gene_symbol":"HDAC11","gene_name":"histone deacetylase 11 [Source:HGNC Symbol;Acc:HGNC:19086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79885","summary":"This gene encodes a class IV histone deacetylase. The encoded protein is localized to the nucleus and may be involved in regulating the expression of interleukin 10. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2009]","start":13479724,"end":13506424,"strand":1,"description":"histone deacetylase 11 [Source:HGNC Symbol;Acc:HGNC:19086]"}, {"versioned_ensembl_gene_id":"ENSG00000274274.1","gene_symbol":"GAGE13","gene_name":"G antigen 13 [Source:HGNC Symbol;Acc:HGNC:29081]","synonyms":"OTTHUMG00000024138,GAGE12A","biotype":"protein_coding","ncbi_id":"645051","summary":null,"start":49331616,"end":49338952,"strand":1,"description":"G antigen 13 [Source:HGNC Symbol;Acc:HGNC:29081]"}, {"versioned_ensembl_gene_id":"ENSG00000169064.12","gene_symbol":"ZBBX","gene_name":"zinc finger B-box domain containing [Source:HGNC Symbol;Acc:HGNC:26245]","synonyms":"FLJ23049","biotype":"protein_coding","ncbi_id":"79740","summary":null,"start":167240287,"end":167381346,"strand":-1,"description":"zinc finger B-box domain containing [Source:HGNC Symbol;Acc:HGNC:26245]"}, {"versioned_ensembl_gene_id":"ENSG00000280276.1","gene_symbol":"AC009229.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":38121935,"end":38123881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112837.16","gene_symbol":"TBX18","gene_name":"T-box 18 [Source:HGNC Symbol;Acc:HGNC:11595]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9096","summary":"This genes codes for a member of an evolutionarily conserved family of transcription factors that plays a crucial role in embryonic development. The family is characterized by the presence of the DNA-binding T-box domain and is divided into five sub-families based on sequence conservation in this domain. The encoded protein belongs to the vertebrate specific Tbx1 sub-family. The protein acts as a transcriptional repressor by antagonizing transcriptional activators in the T-box family. The protein forms homo- or heterodimers with other transcription factors of the T-box family or other transcription factors. [provided by RefSeq, Nov 2012]","start":84687351,"end":84764519,"strand":-1,"description":"T-box 18 [Source:HGNC Symbol;Acc:HGNC:11595]"}, {"versioned_ensembl_gene_id":"ENSG00000260174.1","gene_symbol":"AC111152.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30044455,"end":30045296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216781.2","gene_symbol":"AL138885.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10365593,"end":10366582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141027.20","gene_symbol":"NCOR1","gene_name":"nuclear receptor corepressor 1 [Source:HGNC Symbol;Acc:HGNC:7672]","synonyms":"TRAC1,PPP1R109,N-CoR,MGC104216,KIAA1047,hN-CoR,hCIT529I10","biotype":"protein_coding","ncbi_id":"9611","summary":"This gene encodes a protein that mediates ligand-independent transcription repression of thyroid-hormone and retinoic-acid receptors by promoting chromatin condensation and preventing access of the transcription machinery. It is part of a complex which also includes histone deacetylases and transcriptional regulators similar to the yeast protein Sin3p. This gene is located between the Charcot-Marie-Tooth and Smith-Magenis syndrome critical regions on chromosome 17. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 17 and 20.[provided by RefSeq, Jun 2010]","start":16029157,"end":16218185,"strand":-1,"description":"nuclear receptor corepressor 1 [Source:HGNC Symbol;Acc:HGNC:7672]"}, {"versioned_ensembl_gene_id":"ENSG00000266936.1","gene_symbol":"AC011442.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11010917,"end":11016011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174943.9","gene_symbol":"KCTD13","gene_name":"potassium channel tetramerization domain containing 13 [Source:HGNC Symbol;Acc:HGNC:22234]","synonyms":"FKSG86,POLDIP1,PDIP1","biotype":"protein_coding","ncbi_id":"253980","summary":null,"start":29905012,"end":29927035,"strand":-1,"description":"potassium channel tetramerization domain containing 13 [Source:HGNC Symbol;Acc:HGNC:22234]"}, {"versioned_ensembl_gene_id":"ENSG00000167858.12","gene_symbol":"TEKT1","gene_name":"tektin 1 [Source:HGNC Symbol;Acc:HGNC:15534]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83659","summary":"This gene product belongs to the tektin family of proteins. Tektins comprise a family of filament-forming proteins that are coassembled with tubulins to form ciliary and flagellar microtubules. This gene is predominantly expressed in the testis and in mouse, tektin 1 mRNA was localized to the spermatocytes and round spermatids in the seminiferous tubules, indicating that it may play a role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":6789133,"end":6831761,"strand":-1,"description":"tektin 1 [Source:HGNC Symbol;Acc:HGNC:15534]"}, {"versioned_ensembl_gene_id":"ENSG00000223928.1","gene_symbol":"NUP35P1","gene_name":"nucleoporin 35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419066","summary":null,"start":24157835,"end":24158781,"strand":1,"description":"nucleoporin 35 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52370]"}, {"versioned_ensembl_gene_id":"ENSG00000279029.1","gene_symbol":"AL353583.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24481180,"end":24483034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260414.1","gene_symbol":"AC138869.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33154352,"end":33154475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261536.2","gene_symbol":"ABHD17AP9","gene_name":"abhydrolase domain containing 17A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38510]","synonyms":"FAM108A10P","biotype":"unprocessed_pseudogene","ncbi_id":"100132251","summary":null,"start":33140850,"end":33143797,"strand":1,"description":"abhydrolase domain containing 17A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38510]"}, {"versioned_ensembl_gene_id":"ENSG00000225674.1","gene_symbol":"IPO7P2","gene_name":"importin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39838]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128337","summary":null,"start":24122065,"end":24123814,"strand":-1,"description":"importin 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39838]"}, {"versioned_ensembl_gene_id":"ENSG00000092203.13","gene_symbol":"TOX4","gene_name":"TOX high mobility group box family member 4 [Source:HGNC Symbol;Acc:HGNC:20161]","synonyms":"LCP1,KIAA0737,C14orf92","biotype":"protein_coding","ncbi_id":"9878","summary":null,"start":21476597,"end":21499175,"strand":1,"description":"TOX high mobility group box family member 4 [Source:HGNC Symbol;Acc:HGNC:20161]"}, {"versioned_ensembl_gene_id":"ENSG00000257818.1","gene_symbol":"C1GALT1P1","gene_name":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729409","summary":null,"start":69284397,"end":69285485,"strand":1,"description":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51614]"}, {"versioned_ensembl_gene_id":"ENSG00000243429.1","gene_symbol":"AF186996.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125712139,"end":125713045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168389.17","gene_symbol":"MFSD2A","gene_name":"major facilitator superfamily domain containing 2A [Source:HGNC Symbol;Acc:HGNC:25897]","synonyms":"MFSD2,FLJ14490","biotype":"protein_coding","ncbi_id":"84879","summary":"The protein encoded by this gene is a transmembrane protein and sodium-dependent lysophosphatidylcholine transporter. The encoded protein is involved in the establishment of the blood-brain barrier and is required for brain growth and function. Defects in this gene are a cause of a progressive microcephaly syndrome. [provided by RefSeq, Mar 2017]","start":39955112,"end":39969968,"strand":1,"description":"major facilitator superfamily domain containing 2A [Source:HGNC Symbol;Acc:HGNC:25897]"}, {"versioned_ensembl_gene_id":"ENSG00000102109.8","gene_symbol":"PCSK1N","gene_name":"proprotein convertase subtilisin/kexin type 1 inhibitor [Source:HGNC Symbol;Acc:HGNC:17301]","synonyms":"SgVIII,SCG8,SAAS,proSAAS,PEN,BigLEN","biotype":"protein_coding","ncbi_id":"27344","summary":"The protein encoded by this gene functions as an inhibitor of prohormone convertase 1, which regulates the proteolytic cleavage of neuroendocrine peptide precursors. The proprotein is further processed into multiple short peptides. A polymorphism within this gene may be associated with obesity. [provided by RefSeq, Aug 2013]","start":48831094,"end":48835633,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 1 inhibitor [Source:HGNC Symbol;Acc:HGNC:17301]"}, {"versioned_ensembl_gene_id":"ENSG00000261968.3","gene_symbol":"KRTAP4-8","gene_name":"keratin associated protein 4-8 [Source:NCBI gene;Acc:728224]","synonyms":"KAP4.8,KAP4.8,KRTAP4.8","biotype":"protein_coding","ncbi_id":"728224","summary":null,"start":41097371,"end":41098544,"strand":-1,"description":"keratin associated protein 4-8 [Source:NCBI gene;Acc:728224]"}, {"versioned_ensembl_gene_id":"ENSG00000226420.1","gene_symbol":"IGLV3-4","gene_name":"immunoglobulin lambda variable 3-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5915]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28807","summary":null,"start":22858025,"end":22858268,"strand":1,"description":"immunoglobulin lambda variable 3-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5915]"}, {"versioned_ensembl_gene_id":"ENSG00000283259.1","gene_symbol":"AC242022.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2773603,"end":2776473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213901.10","gene_symbol":"SLC23A3","gene_name":"solute carrier family 23 member 3 [Source:HGNC Symbol;Acc:HGNC:20601]","synonyms":"Yspl1,SVCT3,FLJ31168","biotype":"protein_coding","ncbi_id":"151295","summary":null,"start":219161465,"end":219170095,"strand":-1,"description":"solute carrier family 23 member 3 [Source:HGNC Symbol;Acc:HGNC:20601]"}, {"versioned_ensembl_gene_id":"ENSG00000109458.8","gene_symbol":"GAB1","gene_name":"GRB2 associated binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2549","summary":"The protein encoded by this gene is a member of the IRS1-like multisubstrate docking protein family. It is an important mediator of branching tubulogenesis and plays a central role in cellular growth response, transformation and apoptosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":143336762,"end":143474568,"strand":1,"description":"GRB2 associated binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4066]"}, {"versioned_ensembl_gene_id":"ENSG00000226477.1","gene_symbol":"AC245028.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22814671,"end":22814926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282063.1","gene_symbol":"RPL23AP95","gene_name":"ribosomal protein L23a pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:51630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480338","summary":null,"start":103152009,"end":103152327,"strand":-1,"description":"ribosomal protein L23a pseudogene 95 [Source:HGNC Symbol;Acc:HGNC:51630]"}, {"versioned_ensembl_gene_id":"ENSG00000227322.11","gene_symbol":"RXRB","gene_name":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]","synonyms":"H-2RIIBP,RCoR-1,NR2B2","biotype":"protein_coding","ncbi_id":"6257","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":33115214,"end":33122477,"strand":-1,"description":"retinoid X receptor beta [Source:HGNC Symbol;Acc:HGNC:10478]"}, {"versioned_ensembl_gene_id":"ENSG00000261664.5","gene_symbol":"TTC39A-AS1","gene_name":"TTC39A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40851]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724097","summary":null,"start":51329654,"end":51335324,"strand":1,"description":"TTC39A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40851]"}, {"versioned_ensembl_gene_id":"ENSG00000243660.9","gene_symbol":"ZNF487","gene_name":"zinc finger protein 487 [Source:HGNC Symbol;Acc:HGNC:23488]","synonyms":"ZNF487P,KRBO1","biotype":"protein_coding","ncbi_id":"642819","summary":null,"start":43436841,"end":43483179,"strand":1,"description":"zinc finger protein 487 [Source:HGNC Symbol;Acc:HGNC:23488]"}, {"versioned_ensembl_gene_id":"ENSG00000167815.11","gene_symbol":"PRDX2","gene_name":"peroxiredoxin 2 [Source:HGNC Symbol;Acc:HGNC:9353]","synonyms":"TSA,TDPX1,PRXII,PRX2,PRP,NKEFB,MGC4104","biotype":"protein_coding","ncbi_id":"7001","summary":"This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein plays an antioxidant protective role in cells, and it may contribute to the antiviral activity of CD8(+) T-cells. The crystal structure of this protein has been resolved to 2.7 angstroms. This protein prevents hemolytic anemia from oxidative stress by stabilizing hemoglobin, thus making this gene a therapeutic target for patients with hemolytic anemia. This protein may have a proliferative effect and play a role in cancer development or progression. Related pseudogenes have been identified on chromosomes 5, 6, 10 and 13. [provided by RefSeq, Mar 2013]","start":12796820,"end":12801859,"strand":-1,"description":"peroxiredoxin 2 [Source:HGNC Symbol;Acc:HGNC:9353]"}, {"versioned_ensembl_gene_id":"ENSG00000091732.15","gene_symbol":"ZC3HC1","gene_name":"zinc finger C3HC-type containing 1 [Source:HGNC Symbol;Acc:HGNC:29913]","synonyms":"NIPA","biotype":"protein_coding","ncbi_id":"51530","summary":"This gene encodes an F-box-containing protein that is a component of an SCF-type E3 ubiquitin ligase complex that regulates the onset of cell division. The G2/M transition in the cell cycle requires the interaction of the proteins cyclin B1 and cyclin-dependent kinase 1. The activated ubiquitin ligase complex targets the protein cyclin B1 for degradation, preventing this transition to mitosis. [provided by RefSeq, Aug 2013]","start":130018286,"end":130051451,"strand":-1,"description":"zinc finger C3HC-type containing 1 [Source:HGNC Symbol;Acc:HGNC:29913]"}, {"versioned_ensembl_gene_id":"ENSG00000253786.1","gene_symbol":"IGLV3-15","gene_name":"immunoglobulin lambda variable 3-15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5900]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28800","summary":null,"start":22755554,"end":22755797,"strand":1,"description":"immunoglobulin lambda variable 3-15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5900]"}, {"versioned_ensembl_gene_id":"ENSG00000225690.1","gene_symbol":"TREML5P","gene_name":"triggering receptor expressed on myeloid cells like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:30808]","synonyms":"TREML2P1,TREML2P,TLT5","biotype":"unprocessed_pseudogene","ncbi_id":"221438","summary":null,"start":41247369,"end":41249649,"strand":1,"description":"triggering receptor expressed on myeloid cells like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:30808]"}, {"versioned_ensembl_gene_id":"ENSG00000234083.1","gene_symbol":"AJ006995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27954922,"end":27985295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171488.14","gene_symbol":"LRRC8C","gene_name":"leucine rich repeat containing 8 family member C [Source:HGNC Symbol;Acc:HGNC:25075]","synonyms":"AD158","biotype":"protein_coding","ncbi_id":"84230","summary":null,"start":89633072,"end":89769903,"strand":1,"description":"leucine rich repeat containing 8 family member C [Source:HGNC Symbol;Acc:HGNC:25075]"}, {"versioned_ensembl_gene_id":"ENSG00000253818.1","gene_symbol":"IGLV1-41","gene_name":"immunoglobulin lambda variable 1-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5878]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28824","summary":null,"start":22404207,"end":22404721,"strand":1,"description":"immunoglobulin lambda variable 1-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5878]"}, {"versioned_ensembl_gene_id":"ENSG00000115289.13","gene_symbol":"PCGF1","gene_name":"polycomb group ring finger 1 [Source:HGNC Symbol;Acc:HGNC:17615]","synonyms":"RNF68,NSPC1,MGC10882","biotype":"protein_coding","ncbi_id":"84759","summary":"PCGF1 is a mammalian homolog of the Drosophila polycomb group genes, which act as transcriptional repressors to regulate anterior-posterior patterning in early embryonic development (Nunes et al., 2001 [PubMed 11287196]). See also PCGF2 (MIM 600346).[supplied by OMIM, Aug 2008]","start":74505043,"end":74508580,"strand":-1,"description":"polycomb group ring finger 1 [Source:HGNC Symbol;Acc:HGNC:17615]"}, {"versioned_ensembl_gene_id":"ENSG00000279274.2","gene_symbol":"AC012005.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24362335,"end":24362409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007923.15","gene_symbol":"DNAJC11","gene_name":"DnaJ heat shock protein family (Hsp40) member C11 [Source:HGNC Symbol;Acc:HGNC:25570]","synonyms":"FLJ10737","biotype":"protein_coding","ncbi_id":"55735","summary":null,"start":6634168,"end":6701924,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C11 [Source:HGNC Symbol;Acc:HGNC:25570]"}, {"versioned_ensembl_gene_id":"ENSG00000237757.2","gene_symbol":"EEF1A1P30","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:37906]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402420","summary":null,"start":120210461,"end":120212680,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:37906]"}, {"versioned_ensembl_gene_id":"ENSG00000279889.1","gene_symbol":"AC012183.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58705799,"end":58706297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006757.11","gene_symbol":"PNPLA4","gene_name":"patatin like phospholipase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24887]","synonyms":"iPLA2eta,GS2,DXS1283E","biotype":"protein_coding","ncbi_id":"8228","summary":"This gene encodes a member of the patatin-like family of phospholipases. The encoded enzyme has both triacylglycerol lipase and transacylase activities and may be involved in adipocyte triglyceride homeostasis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome Y. [provided by RefSeq, Feb 2010]","start":7898247,"end":7927739,"strand":-1,"description":"patatin like phospholipase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24887]"}, {"versioned_ensembl_gene_id":"ENSG00000224827.1","gene_symbol":"LINC00265-2P","gene_name":"long intergenic non-protein coding RNA 265-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38523]","synonyms":"NCRNA00265B,NCRNA00265-2P","biotype":"processed_pseudogene","ncbi_id":"100287296","summary":null,"start":24276245,"end":24277026,"strand":1,"description":"long intergenic non-protein coding RNA 265-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38523]"}, {"versioned_ensembl_gene_id":"ENSG00000276534.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54802839,"end":54817200,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000254817.1","gene_symbol":"AC107918.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12033646,"end":12034612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181444.12","gene_symbol":"ZNF467","gene_name":"zinc finger protein 467 [Source:HGNC Symbol;Acc:HGNC:23154]","synonyms":"Zfp467,EZI","biotype":"protein_coding","ncbi_id":"168544","summary":"The protein encoded by this gene is a zinc finger protein whose function has not yet been elucidated in humans. However, the mouse ortholog of this protein enhances adipocyte differentiation and suppresses osteoblast differentiation in bone marrow. The mouse protein also is a transcription factor for several genes and can help recruit histone deacetylase complexes. [provided by RefSeq, Aug 2016]","start":149764182,"end":149773479,"strand":-1,"description":"zinc finger protein 467 [Source:HGNC Symbol;Acc:HGNC:23154]"}, {"versioned_ensembl_gene_id":"ENSG00000178394.4","gene_symbol":"HTR1A","gene_name":"5-hydroxytryptamine receptor 1A [Source:HGNC Symbol;Acc:HGNC:5286]","synonyms":"ADRBRL1,ADRB2RL1,5-HT1A","biotype":"protein_coding","ncbi_id":"3350","summary":"This gene encodes a G protein-coupled receptor for 5-hydroxytryptamine (serotonin), and belongs to the 5-hydroxytryptamine receptor subfamily. Serotonin has been implicated in a number of physiologic processes and pathologic conditions. Inactivation of this gene in mice results in behavior consistent with an increased anxiety and stress response. Mutation in the promoter of this gene has been associated with menstrual cycle-dependent periodic fevers. [provided by RefSeq, Jun 2012]","start":63960356,"end":63962507,"strand":-1,"description":"5-hydroxytryptamine receptor 1A [Source:HGNC Symbol;Acc:HGNC:5286]"}, {"versioned_ensembl_gene_id":"ENSG00000253444.1","gene_symbol":"AC245519.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2493876,"end":2512580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272181.1","gene_symbol":"AC012557.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64019508,"end":64019925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166825.13","gene_symbol":"ANPEP","gene_name":"alanyl aminopeptidase, membrane [Source:HGNC Symbol;Acc:HGNC:500]","synonyms":"PEPN,p150,LAP1,gp150,CD13","biotype":"protein_coding","ncbi_id":"290","summary":"Aminopeptidase N is located in the small-intestinal and renal microvillar membrane, and also in other plasma membranes. In the small intestine aminopeptidase N plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastric and pancreatic proteases. Its function in proximal tubular epithelial cells and other cell types is less clear. The large extracellular carboxyterminal domain contains a pentapeptide consensus sequence characteristic of members of the zinc-binding metalloproteinase superfamily. Sequence comparisons with known enzymes of this class showed that CD13 and aminopeptidase N are identical. The latter enzyme was thought to be involved in the metabolism of regulatory peptides by diverse cell types, including small intestinal and renal tubular epithelial cells, macrophages, granulocytes, and synaptic membranes from the CNS. This membrane-bound zinc metalloprotease is known to serve as a receptor for the HCoV-229E alphacoronavirus as well as other non-human coronaviruses. This gene has also been shown to promote angiogenesis, tumor growth, and metastasis and defects in this gene are associated with various types of leukemia and lymphoma. [provided by RefSeq, Apr 2020]","start":89784889,"end":89815401,"strand":-1,"description":"alanyl aminopeptidase, membrane [Source:HGNC Symbol;Acc:HGNC:500]"}, {"versioned_ensembl_gene_id":"ENSG00000282740.1","gene_symbol":"AL021920.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16739938,"end":16750589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198855.6","gene_symbol":"FICD","gene_name":"FIC domain containing [Source:HGNC Symbol;Acc:HGNC:18416]","synonyms":"HYPE,HIP13","biotype":"protein_coding","ncbi_id":"11153","summary":null,"start":108515185,"end":108525837,"strand":1,"description":"FIC domain containing [Source:HGNC Symbol;Acc:HGNC:18416]"}, {"versioned_ensembl_gene_id":"ENSG00000239282.7","gene_symbol":"CASTOR1","gene_name":"cytosolic arginine sensor for mTORC1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:34423]","synonyms":"GATSL3","biotype":"protein_coding","ncbi_id":"652968","summary":null,"start":30285117,"end":30289627,"strand":-1,"description":"cytosolic arginine sensor for mTORC1 subunit 1 [Source:HGNC Symbol;Acc:HGNC:34423]"}, {"versioned_ensembl_gene_id":"ENSG00000147454.13","gene_symbol":"SLC25A37","gene_name":"solute carrier family 25 member 37 [Source:HGNC Symbol;Acc:HGNC:29786]","synonyms":"MSCP,MFRN1,MFRN,HT015","biotype":"protein_coding","ncbi_id":"51312","summary":"SLC25A37 is a solute carrier localized in the mitochondrial inner membrane. It functions as an essential iron importer for the synthesis of mitochondrial heme and iron-sulfur clusters (summary by Chen et al., 2009 [PubMed 19805291]).[supplied by OMIM, Jan 2011]","start":23528805,"end":23575463,"strand":1,"description":"solute carrier family 25 member 37 [Source:HGNC Symbol;Acc:HGNC:29786]"}, {"versioned_ensembl_gene_id":"ENSG00000273603.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54847887,"end":54862123,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000123505.15","gene_symbol":"AMD1","gene_name":"adenosylmethionine decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:457]","synonyms":"SAMDC","biotype":"protein_coding","ncbi_id":"262","summary":"This gene encodes an important intermediate enzyme in polyamine biosynthesis. The polyamines spermine, spermidine, and putrescine are low-molecular-weight aliphatic amines essential for cellular proliferation and tumor promotion. Multiple alternatively spliced transcript variants have been identified. Pseudogenes of this gene are found on chromosomes 5, 6, 10, X and Y. [provided by RefSeq, Dec 2013]","start":110874770,"end":110895713,"strand":1,"description":"adenosylmethionine decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:457]"}, {"versioned_ensembl_gene_id":"ENSG00000227875.2","gene_symbol":"RPL23AP89","gene_name":"ribosomal protein L23a pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:51623]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480336","summary":null,"start":12080293,"end":12080547,"strand":-1,"description":"ribosomal protein L23a pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:51623]"}, {"versioned_ensembl_gene_id":"ENSG00000182351.7","gene_symbol":"CRIP1P4","gene_name":"cysteine rich protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44519]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641457","summary":null,"start":24712292,"end":24712520,"strand":1,"description":"cysteine rich protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44519]"}, {"versioned_ensembl_gene_id":"ENSG00000277997.1","gene_symbol":"AC079779.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":307683,"end":309424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273188.1","gene_symbol":"AL022328.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50191724,"end":50192402,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240519.1","gene_symbol":"AC091675.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26771790,"end":26772140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275678.1","gene_symbol":"AL133320.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":67121605,"end":67123956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269320.1","gene_symbol":"AC073544.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23602567,"end":23603106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269431.1","gene_symbol":"BNIP3P8","gene_name":"BCL2 interacting protein 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49675]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421710","summary":null,"start":23380317,"end":23380876,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49675]"}, {"versioned_ensembl_gene_id":"ENSG00000237057.2","gene_symbol":"LINC02087","gene_name":"long intergenic non-protein coding RNA 2087 [Source:HGNC Symbol;Acc:HGNC:52938]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928567","summary":null,"start":15806241,"end":15817742,"strand":-1,"description":"long intergenic non-protein coding RNA 2087 [Source:HGNC Symbol;Acc:HGNC:52938]"}, {"versioned_ensembl_gene_id":"ENSG00000102034.16","gene_symbol":"ELF4","gene_name":"E74 like ETS transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:3319]","synonyms":"MEF,ELFR","biotype":"protein_coding","ncbi_id":"2000","summary":"The protein encoded by this gene is a transcriptional activator that binds and activates the promoters of the CSF2, IL3, IL8, and PRF1 genes. The encoded protein is involved in natural killer cell development and function, innate immunity, and induction of cell cycle arrest in naive CD8+ cells. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Jan 2010]","start":130064874,"end":130110716,"strand":-1,"description":"E74 like ETS transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:3319]"}, {"versioned_ensembl_gene_id":"ENSG00000005483.20","gene_symbol":"KMT2E","gene_name":"lysine methyltransferase 2E [Source:HGNC Symbol;Acc:HGNC:18541]","synonyms":"MLL5,HDCMC04P","biotype":"protein_coding","ncbi_id":"55904","summary":"This gene is a member of the myeloid/lymphoid or mixed-lineage leukemia (MLL) family and encodes a protein with an N-terminal PHD zinc finger and a central SET domain. Overexpression of the protein inhibits cell cycle progression. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":105014179,"end":105114361,"strand":1,"description":"lysine methyltransferase 2E [Source:HGNC Symbol;Acc:HGNC:18541]"}, {"versioned_ensembl_gene_id":"ENSG00000260803.1","gene_symbol":"Z84723.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":17514,"end":35195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141385.9","gene_symbol":"AFG3L2","gene_name":"AFG3 like matrix AAA peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:315]","synonyms":"SPAX5,SCA28","biotype":"protein_coding","ncbi_id":"10939","summary":"This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]","start":12328944,"end":12377314,"strand":-1,"description":"AFG3 like matrix AAA peptidase subunit 2 [Source:HGNC Symbol;Acc:HGNC:315]"}, {"versioned_ensembl_gene_id":"ENSG00000226942.2","gene_symbol":"IL9RP3","gene_name":"interleukin 9 receptor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:6033]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729486","summary":null,"start":29336,"end":38321,"strand":-1,"description":"interleukin 9 receptor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:6033]"}, {"versioned_ensembl_gene_id":"ENSG00000234769.7","gene_symbol":"WASH4P","gene_name":"WAS protein family homolog 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14126]","synonyms":"FLJ31670,FAM39CP","biotype":"unprocessed_pseudogene","ncbi_id":"374677","summary":null,"start":14381,"end":18068,"strand":-1,"description":"WAS protein family homolog 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:14126]"}, {"versioned_ensembl_gene_id":"ENSG00000023572.8","gene_symbol":"GLRX2","gene_name":"glutaredoxin 2 [Source:HGNC Symbol;Acc:HGNC:16065]","synonyms":"GRX2,bA101E13.1","biotype":"protein_coding","ncbi_id":"51022","summary":"The protein encoded by this gene is a member of the glutaredoxin family of proteins, which maintain cellular thiol homeostasis. These proteins are thiol-disulfide oxidoreductases that use a glutathione-binding site and one or two active cysteines in their active site. This gene undergoes alternative splicing to produce multiple isoforms, one of which is ubiquitously expressed and localizes to mitochondria, where it functions in mitochondrial redox homeostasis and is important for the protection against and recovery from oxidative stress. Other isoforms, which have more restrictive expression patterns, show cytosolic and nuclear localization, and are thought to function in cellular differentiation and transformation, possibly with a role in tumor progression. [provided by RefSeq, Aug 2011]","start":193096468,"end":193106114,"strand":-1,"description":"glutaredoxin 2 [Source:HGNC Symbol;Acc:HGNC:16065]"}, {"versioned_ensembl_gene_id":"ENSG00000259774.1","gene_symbol":"AC243562.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84422618,"end":84425882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268148.1","gene_symbol":"VN1R91P","gene_name":"vomeronasal 1 receptor 91 pseudogene [Source:HGNC Symbol;Acc:HGNC:37411]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312836","summary":null,"start":23290849,"end":23291017,"strand":1,"description":"vomeronasal 1 receptor 91 pseudogene [Source:HGNC Symbol;Acc:HGNC:37411]"}, {"versioned_ensembl_gene_id":"ENSG00000251459.1","gene_symbol":"AC013724.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57491390,"end":57495233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268794.1","gene_symbol":"VN1R90P","gene_name":"vomeronasal 1 receptor 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:37410]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312835","summary":null,"start":23288620,"end":23289345,"strand":1,"description":"vomeronasal 1 receptor 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:37410]"}, {"versioned_ensembl_gene_id":"ENSG00000103145.10","gene_symbol":"HCFC1R1","gene_name":"host cell factor C1 regulator 1 [Source:HGNC Symbol;Acc:HGNC:21198]","synonyms":"HPIP,FLJ20568","biotype":"protein_coding","ncbi_id":"54985","summary":null,"start":3022620,"end":3024286,"strand":-1,"description":"host cell factor C1 regulator 1 [Source:HGNC Symbol;Acc:HGNC:21198]"}, {"versioned_ensembl_gene_id":"ENSG00000087903.12","gene_symbol":"RFX2","gene_name":"regulatory factor X2 [Source:HGNC Symbol;Acc:HGNC:9983]","synonyms":"FLJ14226","biotype":"protein_coding","ncbi_id":"5990","summary":"This gene is a member of the regulatory factor X gene family, which encodes transcription factors that contain a highly-conserved winged helix DNA binding domain. The protein encoded by this gene is structurally related to regulatory factors X1, X3, X4, and X5. It is a transcriptional activator that can bind DNA as a monomer or as a heterodimer with other RFX family members. This protein can bind to cis elements in the promoter of the IL-5 receptor alpha gene. Two transcript variants encoding different isoforms have been described for this gene, and both variants utilize alternative polyadenylation sites. [provided by RefSeq, Jul 2008]","start":5993164,"end":6199572,"strand":-1,"description":"regulatory factor X2 [Source:HGNC Symbol;Acc:HGNC:9983]"}, {"versioned_ensembl_gene_id":"ENSG00000233193.1","gene_symbol":"AC005324.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15761614,"end":15763769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233300.1","gene_symbol":"EIF4A1P1","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3283]","synonyms":"EIF4A1P","biotype":"processed_pseudogene","ncbi_id":"54052","summary":null,"start":27367014,"end":27367947,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3283]"}, {"versioned_ensembl_gene_id":"ENSG00000250400.3","gene_symbol":"LINC00977","gene_name":"long intergenic non-protein coding RNA 977 [Source:HGNC Symbol;Acc:HGNC:48902]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728724","summary":null,"start":129216467,"end":129241250,"strand":-1,"description":"long intergenic non-protein coding RNA 977 [Source:HGNC Symbol;Acc:HGNC:48902]"}, {"versioned_ensembl_gene_id":"ENSG00000239205.1","gene_symbol":"LINC02023","gene_name":"long intergenic non-protein coding RNA 2023 [Source:HGNC Symbol;Acc:HGNC:52858]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928405","summary":null,"start":165150006,"end":165158062,"strand":-1,"description":"long intergenic non-protein coding RNA 2023 [Source:HGNC Symbol;Acc:HGNC:52858]"}, {"versioned_ensembl_gene_id":"ENSG00000115828.15","gene_symbol":"QPCT","gene_name":"glutaminyl-peptide cyclotransferase [Source:HGNC Symbol;Acc:HGNC:9753]","synonyms":"QC,GCT","biotype":"protein_coding","ncbi_id":"25797","summary":"This gene encodes human pituitary glutaminyl cyclase, which is responsible for the presence of pyroglutamyl residues in many neuroendocrine peptides. The amino acid sequence of this enzyme is 86% identical to that of bovine glutaminyl cyclase. [provided by RefSeq, Jul 2008]","start":37344574,"end":37373322,"strand":1,"description":"glutaminyl-peptide cyclotransferase [Source:HGNC Symbol;Acc:HGNC:9753]"}, {"versioned_ensembl_gene_id":"ENSG00000236956.1","gene_symbol":"NF1P8","gene_name":"neurofibromin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:7767]","synonyms":"NF1L2","biotype":"unprocessed_pseudogene","ncbi_id":"401007","summary":null,"start":131189834,"end":131197493,"strand":-1,"description":"neurofibromin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:7767]"}, {"versioned_ensembl_gene_id":"ENSG00000235370.6","gene_symbol":"DNM1P51","gene_name":"dynamin 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48500]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"109729113","summary":null,"start":84398316,"end":84411701,"strand":-1,"description":"dynamin 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48500]"}, {"versioned_ensembl_gene_id":"ENSG00000275511.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54864251,"end":54881045,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000223563.1","gene_symbol":"AP001599.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26889376,"end":26939742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168924.14","gene_symbol":"LETM1","gene_name":"leucine zipper and EF-hand containing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6556]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3954","summary":"This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]","start":1811479,"end":1856247,"strand":-1,"description":"leucine zipper and EF-hand containing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:6556]"}, {"versioned_ensembl_gene_id":"ENSG00000198001.13","gene_symbol":"IRAK4","gene_name":"interleukin 1 receptor associated kinase 4 [Source:HGNC Symbol;Acc:HGNC:17967]","synonyms":"NY-REN-64","biotype":"protein_coding","ncbi_id":"51135","summary":"This gene encodes a kinase that activates NF-kappaB in both the Toll-like receptor (TLR) and T-cell receptor (TCR) signaling pathways. The protein is essential for most innate immune responses. Mutations in this gene result in IRAK4 deficiency and recurrent invasive pneumococcal disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":43758944,"end":43789543,"strand":1,"description":"interleukin 1 receptor associated kinase 4 [Source:HGNC Symbol;Acc:HGNC:17967]"}, {"versioned_ensembl_gene_id":"ENSG00000239941.1","gene_symbol":"AC108718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152118173,"end":152151724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257281.1","gene_symbol":"AC009729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108281103,"end":108282235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277726.4","gene_symbol":"AL109811.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":11012662,"end":11030528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112576.12","gene_symbol":"CCND3","gene_name":"cyclin D3 [Source:HGNC Symbol;Acc:HGNC:1585]","synonyms":null,"biotype":"protein_coding","ncbi_id":"896","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK4 or CDK6, whose activtiy is required for cell cycle G1/S transition. This protein has been shown to interact with and be involved in the phosphorylation of tumor suppressor protein Rb. The CDK4 activity associated with this cyclin was reported to be necessary for cell cycle progression through G2 phase into mitosis after UV radiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":41934933,"end":42050357,"strand":-1,"description":"cyclin D3 [Source:HGNC Symbol;Acc:HGNC:1585]"}, {"versioned_ensembl_gene_id":"ENSG00000229798.1","gene_symbol":"KRT18P26","gene_name":"keratin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33395]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418770","summary":null,"start":74306728,"end":74308008,"strand":-1,"description":"keratin 18 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:33395]"}, {"versioned_ensembl_gene_id":"ENSG00000237737.5","gene_symbol":"DCTN1-AS1","gene_name":"DCTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44151]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100189589","summary":null,"start":74385486,"end":74393882,"strand":1,"description":"DCTN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44151]"}, {"versioned_ensembl_gene_id":"ENSG00000215481.9","gene_symbol":"BCRP3","gene_name":"breakpoint cluster region pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1016]","synonyms":"BCRL6,BCRL3,BCR3","biotype":"processed_transcript","ncbi_id":"644165","summary":null,"start":24632915,"end":24650012,"strand":1,"description":"breakpoint cluster region pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1016]"}, {"versioned_ensembl_gene_id":"ENSG00000276154.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832687,"end":54848602,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000283201.1","gene_symbol":"AC092329.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23222755,"end":23274221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274403.1","gene_symbol":"AC090510.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42726583,"end":42727211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145386.9","gene_symbol":"CCNA2","gene_name":"cyclin A2 [Source:HGNC Symbol;Acc:HGNC:1578]","synonyms":"CCN1,CCNA","biotype":"protein_coding","ncbi_id":"890","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members function as regulators of the cell cycle. This protein binds and activates cyclin-dependent kinase 2 and thus promotes transition through G1/S and G2/M. [provided by RefSeq, Aug 2016]","start":121816444,"end":121823933,"strand":-1,"description":"cyclin A2 [Source:HGNC Symbol;Acc:HGNC:1578]"}, {"versioned_ensembl_gene_id":"ENSG00000073150.13","gene_symbol":"PANX2","gene_name":"pannexin 2 [Source:HGNC Symbol;Acc:HGNC:8600]","synonyms":"PX2,hPANX2","biotype":"protein_coding","ncbi_id":"56666","summary":"The protein encoded by this gene belongs to the innexin family. Innexin family members are the structural components of gap junctions. This protein and pannexin 1 are abundantly expressed in central nervous system (CNS) and are coexpressed in various neuronal populations. Studies in Xenopus oocytes suggest that this protein alone and in combination with pannexin 1 may form cell type-specific gap junctions with distinct properties. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":50170731,"end":50180294,"strand":1,"description":"pannexin 2 [Source:HGNC Symbol;Acc:HGNC:8600]"}, {"versioned_ensembl_gene_id":"ENSG00000220110.1","gene_symbol":"AL080315.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128639188,"end":128639653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263335.1","gene_symbol":"AF001548.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15726674,"end":15732993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186517.13","gene_symbol":"ARHGAP30","gene_name":"Rho GTPase activating protein 30 [Source:HGNC Symbol;Acc:HGNC:27414]","synonyms":"FLJ00267","biotype":"protein_coding","ncbi_id":"257106","summary":null,"start":161046946,"end":161069970,"strand":-1,"description":"Rho GTPase activating protein 30 [Source:HGNC Symbol;Acc:HGNC:27414]"}, {"versioned_ensembl_gene_id":"ENSG00000225132.9","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DP2B,HLA-DP2B,DPB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33034341,"end":33050662,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000118898.15","gene_symbol":"PPL","gene_name":"periplakin [Source:HGNC Symbol;Acc:HGNC:9273]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5493","summary":"The protein encoded by this gene is a component of desmosomes and of the epidermal cornified envelope in keratinocytes. The N-terminal domain of this protein interacts with the plasma membrane and its C-terminus interacts with intermediate filaments. Through its rod domain, this protein forms complexes with envoplakin. This protein may serve as a link between the cornified envelope and desmosomes as well as intermediate filaments. AKT1/PKB, a protein kinase mediating a variety of cell growth and survival signaling processes, is reported to interact with this protein, suggesting a possible role for this protein as a localization signal in AKT1-mediated signaling. [provided by RefSeq, Jul 2008]","start":4882507,"end":4960741,"strand":-1,"description":"periplakin [Source:HGNC Symbol;Acc:HGNC:9273]"}, {"versioned_ensembl_gene_id":"ENSG00000235981.2","gene_symbol":"AC023274.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24142358,"end":24157843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213130.3","gene_symbol":"EEF1DP5","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33524]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442258","summary":null,"start":128580113,"end":128580884,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33524]"}, {"versioned_ensembl_gene_id":"ENSG00000197885.10","gene_symbol":"NKIRAS1","gene_name":"NFKB inhibitor interacting Ras like 1 [Source:HGNC Symbol;Acc:HGNC:17899]","synonyms":"KBRAS1,kappaB-Ras1","biotype":"protein_coding","ncbi_id":"28512","summary":null,"start":23891660,"end":23946591,"strand":-1,"description":"NFKB inhibitor interacting Ras like 1 [Source:HGNC Symbol;Acc:HGNC:17899]"}, {"versioned_ensembl_gene_id":"ENSG00000259299.1","gene_symbol":"AC061965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29233673,"end":29235137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173093.12","gene_symbol":"CCDC63","gene_name":"coiled-coil domain containing 63 [Source:HGNC Symbol;Acc:HGNC:26669]","synonyms":"ODA5,FLJ35843","biotype":"protein_coding","ncbi_id":"160762","summary":null,"start":110846769,"end":110907535,"strand":1,"description":"coiled-coil domain containing 63 [Source:HGNC Symbol;Acc:HGNC:26669]"}, {"versioned_ensembl_gene_id":"ENSG00000104059.4","gene_symbol":"FAM189A1","gene_name":"family with sequence similarity 189 member A1 [Source:HGNC Symbol;Acc:HGNC:29075]","synonyms":"TMEM228,KIAA0574","biotype":"protein_coding","ncbi_id":"23359","summary":null,"start":29120254,"end":29570723,"strand":-1,"description":"family with sequence similarity 189 member A1 [Source:HGNC Symbol;Acc:HGNC:29075]"}, {"versioned_ensembl_gene_id":"ENSG00000214200.2","gene_symbol":"TPM3P2","gene_name":"tropomyosin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16556]","synonyms":"TPM5P,dJ1125A11.2","biotype":"processed_pseudogene","ncbi_id":"170555","summary":null,"start":33912323,"end":33913336,"strand":-1,"description":"tropomyosin 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16556]"}, {"versioned_ensembl_gene_id":"ENSG00000259802.1","gene_symbol":"AC012640.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10352701,"end":10353601,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135637.13","gene_symbol":"CCDC142","gene_name":"coiled-coil domain containing 142 [Source:HGNC Symbol;Acc:HGNC:25889]","synonyms":"FLJ14397","biotype":"protein_coding","ncbi_id":"84865","summary":null,"start":74471986,"end":74483408,"strand":-1,"description":"coiled-coil domain containing 142 [Source:HGNC Symbol;Acc:HGNC:25889]"}, {"versioned_ensembl_gene_id":"ENSG00000266105.1","gene_symbol":"AC009831.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31966960,"end":31967545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277495.4","gene_symbol":"OR13A1","gene_name":"olfactory receptor family 13 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79290","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":45302654,"end":45315608,"strand":-1,"description":"olfactory receptor family 13 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14772]"}, {"versioned_ensembl_gene_id":"ENSG00000237989.1","gene_symbol":"LINC01679","gene_name":"long intergenic non-protein coding RNA 1679 [Source:HGNC Symbol;Acc:HGNC:52469]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928399","summary":null,"start":43358147,"end":43362349,"strand":-1,"description":"long intergenic non-protein coding RNA 1679 [Source:HGNC Symbol;Acc:HGNC:52469]"}, {"versioned_ensembl_gene_id":"ENSG00000099840.13","gene_symbol":"IZUMO4","gene_name":"IZUMO family member 4 [Source:HGNC Symbol;Acc:HGNC:26950]","synonyms":"C19orf36","biotype":"protein_coding","ncbi_id":"113177","summary":null,"start":2096429,"end":2099593,"strand":1,"description":"IZUMO family member 4 [Source:HGNC Symbol;Acc:HGNC:26950]"}, {"versioned_ensembl_gene_id":"ENSG00000275253.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"nkat5,183ActI,CD158J,cl-49","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738498,"end":54752702,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000181819.14","gene_symbol":"KCTD9P2","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29274]","synonyms":"KCTD9L","biotype":"processed_pseudogene","ncbi_id":"643535","summary":null,"start":105405647,"end":105407039,"strand":1,"description":"potassium channel tetramerization domain containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29274]"}, {"versioned_ensembl_gene_id":"ENSG00000223733.1","gene_symbol":"RPL18AP14","gene_name":"ribosomal protein L18a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36624]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271420","summary":null,"start":104803915,"end":104804440,"strand":1,"description":"ribosomal protein L18a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36624]"}, {"versioned_ensembl_gene_id":"ENSG00000147044.20","gene_symbol":"CASK","gene_name":"calcium/calmodulin dependent serine protein kinase [Source:HGNC Symbol;Acc:HGNC:1497]","synonyms":"TNRC8,LIN2,FGS4,CAGH39","biotype":"protein_coding","ncbi_id":"8573","summary":"This gene encodes a calcium/calmodulin-dependent serine protein kinase. The encoded protein is a MAGUK (membrane-associated guanylate kinase) protein family member. These proteins are scaffold proteins and the encoded protein is located at synapses in the brain. Mutations in this gene are associated with FG syndrome 4, intellectual disability and microcephaly with pontine and cerebellar hypoplasia, and a form of X-linked intellectual disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":41514934,"end":41923463,"strand":-1,"description":"calcium/calmodulin dependent serine protein kinase [Source:HGNC Symbol;Acc:HGNC:1497]"}, {"versioned_ensembl_gene_id":"ENSG00000227937.1","gene_symbol":"MTND2P30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42131]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873234","summary":null,"start":81080790,"end":81081171,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42131]"}, {"versioned_ensembl_gene_id":"ENSG00000239280.1","gene_symbol":"AC108693.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113740823,"end":113741254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251515.1","gene_symbol":"CCDC11P1","gene_name":"coiled-coil domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129040","summary":null,"start":39571478,"end":39572639,"strand":-1,"description":"coiled-coil domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43919]"}, {"versioned_ensembl_gene_id":"ENSG00000213150.2","gene_symbol":"AL512430.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110645699,"end":110646558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232019.1","gene_symbol":"AC074183.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84939349,"end":84940245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243396.1","gene_symbol":"AC084198.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101599243,"end":101599644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075218.18","gene_symbol":"GTSE1","gene_name":"G2 and S-phase expressed 1 [Source:HGNC Symbol;Acc:HGNC:13698]","synonyms":"GTSE-1,B99","biotype":"protein_coding","ncbi_id":"51512","summary":"The protein encoded by this gene is only expressed in the S and G2 phases of the cell cycle, where it colocalizes with cytoplasmic tubulin and microtubules. In response to DNA damage, the encoded protein accumulates in the nucleus and binds the tumor suppressor protein p53, shuttling it out of the nucleus and repressing its ability to induce apoptosis. [provided by RefSeq, Jul 2008]","start":46296741,"end":46330810,"strand":1,"description":"G2 and S-phase expressed 1 [Source:HGNC Symbol;Acc:HGNC:13698]"}, {"versioned_ensembl_gene_id":"ENSG00000122034.14","gene_symbol":"GTF3A","gene_name":"general transcription factor IIIA [Source:HGNC Symbol;Acc:HGNC:4662]","synonyms":"TFIIIA,AP2","biotype":"protein_coding","ncbi_id":"2971","summary":"The product of this gene is a zinc finger protein with nine Cis[2]-His[2] zinc finger domains. It functions as an RNA polymerase III transcription factor to induce transcription of the 5S rRNA genes. The protein binds to a 50 bp internal promoter in the 5S genes called the internal control region (ICR), and nucleates formation of a stable preinitiation complex. This complex recruits the TFIIIC and TFIIIB transcription factors and RNA polymerase III to form the complete transcription complex. The protein is thought to be translated using a non-AUG translation initiation site in mammals based on sequence analysis, protein homology, and the size of the purified protein. [provided by RefSeq, Jul 2008]","start":27424544,"end":27435823,"strand":1,"description":"general transcription factor IIIA [Source:HGNC Symbol;Acc:HGNC:4662]"}, {"versioned_ensembl_gene_id":"ENSG00000261798.1","gene_symbol":"AL033527.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39788976,"end":39790171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158773.14","gene_symbol":"USF1","gene_name":"upstream transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12593]","synonyms":"MLTFI,bHLHb11,UEF","biotype":"protein_coding","ncbi_id":"7391","summary":"This gene encodes a member of the basic helix-loop-helix leucine zipper family, and can function as a cellular transcription factor. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs. This gene has been linked to familial combined hyperlipidemia (FCHL). Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been defined on chromosome 21. [provided by RefSeq, Feb 2013]","start":161039251,"end":161045977,"strand":-1,"description":"upstream transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:12593]"}, {"versioned_ensembl_gene_id":"ENSG00000099985.3","gene_symbol":"OSM","gene_name":"oncostatin M [Source:HGNC Symbol;Acc:HGNC:8506]","synonyms":"MGC20461","biotype":"protein_coding","ncbi_id":"5008","summary":"This gene encodes a member of the leukemia inhibitory factor/oncostatin-M (LIF/OSM) family of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a secreted cytokine and growth regulator that inhibits the proliferation of a number of tumor cell lines. This protein also regulates the production of other cytokines, including interleukin 6, granulocyte-colony stimulating factor and granulocyte-macrophage colony stimulating factor in endothelial cells. This gene and the related gene, leukemia inhibitory factor, also present on chromosome 22, may have resulted from the duplication of a common ancestral gene. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":30262829,"end":30266840,"strand":-1,"description":"oncostatin M [Source:HGNC Symbol;Acc:HGNC:8506]"}, {"versioned_ensembl_gene_id":"ENSG00000279181.1","gene_symbol":"AC110801.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73998337,"end":73998548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268105.1","gene_symbol":"AC124856.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23125665,"end":23128543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267920.1","gene_symbol":"SNX6P1","gene_name":"sorting nexin 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41511]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"126506","summary":null,"start":23126569,"end":23127792,"strand":-1,"description":"sorting nexin 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41511]"}, {"versioned_ensembl_gene_id":"ENSG00000224215.1","gene_symbol":"AL606469.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23343957,"end":23345181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000038002.8","gene_symbol":"AGA","gene_name":"aspartylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:318]","synonyms":"ASRG","biotype":"protein_coding","ncbi_id":"175","summary":"This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing. [provided by RefSeq, Nov 2015]","start":177430770,"end":177442503,"strand":-1,"description":"aspartylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:318]"}, {"versioned_ensembl_gene_id":"ENSG00000135821.17","gene_symbol":"GLUL","gene_name":"glutamate-ammonia ligase [Source:HGNC Symbol;Acc:HGNC:4341]","synonyms":"GLNS","biotype":"protein_coding","ncbi_id":"2752","summary":"The protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. This protein plays a role in ammonia and glutamate detoxification, acid-base homeostasis, cell signaling, and cell proliferation. Glutamine is an abundant amino acid, and is important to the biosynthesis of several amino acids, pyrimidines, and purines. Mutations in this gene are associated with congenital glutamine deficiency, and overexpression of this gene was observed in some primary liver cancer samples. There are six pseudogenes of this gene found on chromosomes 2, 5, 9, 11, and 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":182381704,"end":182392206,"strand":-1,"description":"glutamate-ammonia ligase [Source:HGNC Symbol;Acc:HGNC:4341]"}, {"versioned_ensembl_gene_id":"ENSG00000261135.1","gene_symbol":"AL137802.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16514645,"end":16515754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268541.1","gene_symbol":"VN1R88P","gene_name":"vomeronasal 1 receptor 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:37408]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312833","summary":null,"start":22861303,"end":22861594,"strand":1,"description":"vomeronasal 1 receptor 88 pseudogene [Source:HGNC Symbol;Acc:HGNC:37408]"}, {"versioned_ensembl_gene_id":"ENSG00000227881.1","gene_symbol":"ASS1P5","gene_name":"argininosuccinate synthetase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:768]","synonyms":"ASSP5","biotype":"processed_pseudogene","ncbi_id":"450","summary":null,"start":115664895,"end":115666133,"strand":1,"description":"argininosuccinate synthetase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:768]"}, {"versioned_ensembl_gene_id":"ENSG00000260644.6","gene_symbol":"HERC2P5","gene_name":"hect domain and RLD 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4873]","synonyms":"D16F37S6","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388254","summary":null,"start":32741314,"end":32776196,"strand":1,"description":"hect domain and RLD 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4873]"}, {"versioned_ensembl_gene_id":"ENSG00000268696.1","gene_symbol":"ZNF723","gene_name":"zinc finger protein 723 [Source:HGNC Symbol;Acc:HGNC:32286]","synonyms":"ZNF723P","biotype":"unprocessed_pseudogene","ncbi_id":"646864","summary":null,"start":22832201,"end":22859422,"strand":1,"description":"zinc finger protein 723 [Source:HGNC Symbol;Acc:HGNC:32286]"}, {"versioned_ensembl_gene_id":"ENSG00000271655.1","gene_symbol":"BNIP3P35","gene_name":"BCL2 interacting protein 3 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:49715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480284","summary":null,"start":22840432,"end":22840921,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:49715]"}, {"versioned_ensembl_gene_id":"ENSG00000101997.12","gene_symbol":"CCDC22","gene_name":"coiled-coil domain containing 22 [Source:HGNC Symbol;Acc:HGNC:28909]","synonyms":"JM1,CXorf37","biotype":"protein_coding","ncbi_id":"28952","summary":"This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]","start":49235467,"end":49250526,"strand":1,"description":"coiled-coil domain containing 22 [Source:HGNC Symbol;Acc:HGNC:28909]"}, {"versioned_ensembl_gene_id":"ENSG00000177143.4","gene_symbol":"CETN1","gene_name":"centrin 1 [Source:HGNC Symbol;Acc:HGNC:1866]","synonyms":"CETN,CEN1","biotype":"protein_coding","ncbi_id":"1068","summary":"The protein encoded by this gene plays important roles in the determination of centrosome position and segregation, and in the process of microtubule severing. This protein is localized to the centrosome of interphase cells, and redistributes to the region of the spindle poles during mitosis, reflecting the dynamic behavior of the centrosome during the cell cycle. [provided by RefSeq, Jan 2015]","start":580357,"end":582114,"strand":1,"description":"centrin 1 [Source:HGNC Symbol;Acc:HGNC:1866]"}, {"versioned_ensembl_gene_id":"ENSG00000270431.1","gene_symbol":"AC005000.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115659713,"end":115660022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173264.14","gene_symbol":"GPR137","gene_name":"G protein-coupled receptor 137 [Source:HGNC Symbol;Acc:HGNC:24300]","synonyms":"TM7SF1L1,GPR137A,C11orf4","biotype":"protein_coding","ncbi_id":"56834","summary":null,"start":64270062,"end":64289500,"strand":1,"description":"G protein-coupled receptor 137 [Source:HGNC Symbol;Acc:HGNC:24300]"}, {"versioned_ensembl_gene_id":"ENSG00000163513.17","gene_symbol":"TGFBR2","gene_name":"transforming growth factor beta receptor 2 [Source:HGNC Symbol;Acc:HGNC:11773]","synonyms":"MFS2","biotype":"protein_coding","ncbi_id":"7048","summary":"The protein encoded by this gene is a transmembrane protein that has a protein kinase domain, forms a heterodimeric complex with TGF-beta receptor type-1, and binds TGF-beta. This receptor/ligand complex phosphorylates proteins, which then enter the nucleus and regulate the transcription of genes related to cell proliferation, cell cycle arrest, wound healing, immunosuppression, and tumorigenesis. Mutations in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome, and the development of various types of tumors. Alternatively spliced transcript variants encoding different isoforms have been characterized. [provided by RefSeq, Aug 2017]","start":30606502,"end":30694142,"strand":1,"description":"transforming growth factor beta receptor 2 [Source:HGNC Symbol;Acc:HGNC:11773]"}, {"versioned_ensembl_gene_id":"ENSG00000255581.1","gene_symbol":"AC006511.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8017201,"end":8017860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255964.1","gene_symbol":"HSPD1P12","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35140]","synonyms":"HSPD1-10P","biotype":"processed_pseudogene","ncbi_id":"283320","summary":null,"start":8015024,"end":8016406,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35140]"}, {"versioned_ensembl_gene_id":"ENSG00000240739.1","gene_symbol":"AC006511.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7994770,"end":7995084,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260746.2","gene_symbol":"KIF18BP1","gene_name":"kinesin family member 18B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51808]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642683","summary":null,"start":35636687,"end":35645180,"strand":-1,"description":"kinesin family member 18B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51808]"}, {"versioned_ensembl_gene_id":"ENSG00000259791.1","gene_symbol":"AC092325.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35640029,"end":35640582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162188.5","gene_symbol":"GNG3","gene_name":"G protein subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:4405]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2785","summary":"Guanine nucleotide binding proteins are heterotrimeric signal-transducing molecules consisting of alpha, beta, and gamma subunits. The gamma subunit determines the specificity of which signaling pathways will be affected by this particular complex. The protein encoded by this gene represents the gamma subunit of both inhibitory and stimulatory complexes. [provided by RefSeq, Jan 2012]","start":62707658,"end":62709201,"strand":1,"description":"G protein subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:4405]"}, {"versioned_ensembl_gene_id":"ENSG00000114771.13","gene_symbol":"AADAC","gene_name":"arylacetamide deacetylase [Source:HGNC Symbol;Acc:HGNC:17]","synonyms":"DAC,CES5A1","biotype":"protein_coding","ncbi_id":"13","summary":"Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens [provided by RefSeq, Jul 2008]","start":151814037,"end":151828488,"strand":1,"description":"arylacetamide deacetylase [Source:HGNC Symbol;Acc:HGNC:17]"}, {"versioned_ensembl_gene_id":"ENSG00000124641.15","gene_symbol":"MED20","gene_name":"mediator complex subunit 20 [Source:HGNC Symbol;Acc:HGNC:16840]","synonyms":"TRFP,SRB2,PRO0213,DKFZp586D2223","biotype":"protein_coding","ncbi_id":"9477","summary":"This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. A mutation in this gene has been associated with a novel infantile-onset neurodegenerative movement disorder. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]","start":41905354,"end":41921139,"strand":-1,"description":"mediator complex subunit 20 [Source:HGNC Symbol;Acc:HGNC:16840]"}, {"versioned_ensembl_gene_id":"ENSG00000269622.1","gene_symbol":"TP53TG3HP","gene_name":"TP53 target 3 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51819]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100130700","summary":null,"start":35506592,"end":35507170,"strand":-1,"description":"TP53 target 3 family member H, pseudogene [Source:HGNC Symbol;Acc:HGNC:51819]"}, {"versioned_ensembl_gene_id":"ENSG00000116871.15","gene_symbol":"MAP7D1","gene_name":"MAP7 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25514]","synonyms":"RPRC1,PARCC1,FLJ39022,FLJ10350","biotype":"protein_coding","ncbi_id":"55700","summary":null,"start":36155579,"end":36180849,"strand":1,"description":"MAP7 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25514]"}, {"versioned_ensembl_gene_id":"ENSG00000250381.1","gene_symbol":"UNC93B4","gene_name":"unc-93 homolog B4 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13484]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643384","summary":null,"start":4143458,"end":4150421,"strand":-1,"description":"unc-93 homolog B4 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13484]"}, {"versioned_ensembl_gene_id":"ENSG00000226651.6","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31770035,"end":31779217,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000228702.1","gene_symbol":"AL645998.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45725694,"end":45726038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263235.1","gene_symbol":"AC006111.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3650636,"end":3651703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248480.1","gene_symbol":"AC093801.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176631392,"end":176633231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174574.15","gene_symbol":"AKIRIN1","gene_name":"akirin 1 [Source:HGNC Symbol;Acc:HGNC:25744]","synonyms":"FLJ12666,C1orf108","biotype":"protein_coding","ncbi_id":"79647","summary":null,"start":38991223,"end":39006059,"strand":1,"description":"akirin 1 [Source:HGNC Symbol;Acc:HGNC:25744]"}, {"versioned_ensembl_gene_id":"ENSG00000255152.8","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31740020,"end":31764851,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000254002.1","gene_symbol":"AC012574.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23726331,"end":23743042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251281.1","gene_symbol":"AC034223.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33011322,"end":33017607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157833.12","gene_symbol":"GAREM2","gene_name":"GRB2 associated regulator of MAPK1 subtype 2 [Source:HGNC Symbol;Acc:HGNC:27172]","synonyms":"KIAA2038,GAREML,FLJ00375,FAM59B","biotype":"protein_coding","ncbi_id":"150946","summary":null,"start":26173091,"end":26189663,"strand":1,"description":"GRB2 associated regulator of MAPK1 subtype 2 [Source:HGNC Symbol;Acc:HGNC:27172]"}, {"versioned_ensembl_gene_id":"ENSG00000225982.1","gene_symbol":"AL355482.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182086551,"end":182090112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275611.1","gene_symbol":"AL159153.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":110429026,"end":110429342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257813.2","gene_symbol":"AC090525.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43569769,"end":43572038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218732.1","gene_symbol":"AL035633.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72316599,"end":72317436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223394.2","gene_symbol":"TRBV29OR9-2","gene_name":"T-cell receptor beta variable 29/OR9-2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12211]","synonyms":"TCRBV29S2,TRBV29/OR9-2,TCRBV4S2O,TCRBV4O","biotype":"TR_V_pseudogene","ncbi_id":"6958","summary":null,"start":33786221,"end":33786828,"strand":1,"description":"T-cell receptor beta variable 29/OR9-2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12211]"}, {"versioned_ensembl_gene_id":"ENSG00000229609.1","gene_symbol":"LINC01079","gene_name":"long intergenic non-protein coding RNA 1079 [Source:HGNC Symbol;Acc:HGNC:49122]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106146146","summary":null,"start":27373348,"end":27374366,"strand":1,"description":"long intergenic non-protein coding RNA 1079 [Source:HGNC Symbol;Acc:HGNC:49122]"}, {"versioned_ensembl_gene_id":"ENSG00000274636.2","gene_symbol":"GLIS2","gene_name":"GLIS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:29450]","synonyms":"NPHP7","biotype":"protein_coding","ncbi_id":"84662","summary":"This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010]","start":4314761,"end":4339597,"strand":1,"description":"GLIS family zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:29450]"}, {"versioned_ensembl_gene_id":"ENSG00000227379.2","gene_symbol":"PPIAP2","gene_name":"peptidylprolyl isomerase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16542]","synonyms":"bA384D7.2","biotype":"processed_pseudogene","ncbi_id":"170537","summary":null,"start":25368275,"end":25368766,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16542]"}, {"versioned_ensembl_gene_id":"ENSG00000233846.2","gene_symbol":"AL133480.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6278667,"end":6279153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182255.6","gene_symbol":"KCNA4","gene_name":"potassium voltage-gated channel subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:6222]","synonyms":"Kv1.4,KCNA4L,HPCN2,HK1","biotype":"protein_coding","ncbi_id":"3739","summary":"Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the A-type potassium current class, the members of which may be important in the regulation of the fast repolarizing phase of action potentials in heart and thus may influence the duration of cardiac action potential.[provided by RefSeq, Mar 2011]","start":30009741,"end":30017023,"strand":-1,"description":"potassium voltage-gated channel subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:6222]"}, {"versioned_ensembl_gene_id":"ENSG00000237951.1","gene_symbol":"PPIL1P1","gene_name":"peptidylprolyl isomerase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20865]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"150947","summary":null,"start":26162056,"end":26162554,"strand":1,"description":"peptidylprolyl isomerase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20865]"}, {"versioned_ensembl_gene_id":"ENSG00000198829.6","gene_symbol":"SUCNR1","gene_name":"succinate receptor 1 [Source:HGNC Symbol;Acc:HGNC:4542]","synonyms":"GPR91","biotype":"protein_coding","ncbi_id":"56670","summary":"This gene encodes a G-protein-coupled receptor for succinate, an intermediate molecule of the citric acid cycle. It is involved in the promotion of hematopoietic progenitor cell development, and it has a potential role in renovascular hypertension which has known correlations to renal failure, diabetes and atherosclerosis. [provided by RefSeq, Oct 2009]","start":151873643,"end":151884619,"strand":1,"description":"succinate receptor 1 [Source:HGNC Symbol;Acc:HGNC:4542]"}, {"versioned_ensembl_gene_id":"ENSG00000281195.1","gene_symbol":"AC007878.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":71373938,"end":71376320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272692.1","gene_symbol":"AC010997.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75409157,"end":75411842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273248.1","gene_symbol":"AC010997.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75408973,"end":75409326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111412.5","gene_symbol":"C12orf49","gene_name":"chromosome 12 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:26128]","synonyms":"FLJ21415","biotype":"protein_coding","ncbi_id":"79794","summary":null,"start":116710185,"end":116738070,"strand":-1,"description":"chromosome 12 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:26128]"}, {"versioned_ensembl_gene_id":"ENSG00000226051.6","gene_symbol":"ZNF503-AS1","gene_name":"ZNF503 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27370]","synonyms":null,"biotype":"lincRNA","ncbi_id":"253264","summary":null,"start":75269819,"end":75373500,"strand":1,"description":"ZNF503 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27370]"}, {"versioned_ensembl_gene_id":"ENSG00000257767.2","gene_symbol":"AC002996.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":111753890,"end":111791418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259196.1","gene_symbol":"HMBOX1-IT1","gene_name":"HMBOX1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43632]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106481795","summary":null,"start":28949676,"end":28955955,"strand":1,"description":"HMBOX1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43632]"}, {"versioned_ensembl_gene_id":"ENSG00000227549.1","gene_symbol":"AC116035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30524990,"end":30526213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233002.2","gene_symbol":"AC005324.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15735023,"end":15749192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280107.1","gene_symbol":"AL022393.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":28170845,"end":28172521,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160917.14","gene_symbol":"CPSF4","gene_name":"cleavage and polyadenylation specific factor 4 [Source:HGNC Symbol;Acc:HGNC:2327]","synonyms":"NAR,CPSF30","biotype":"protein_coding","ncbi_id":"10898","summary":"Inhibition of the nuclear export of poly(A)-containing mRNAs caused by the influenza A virus NS1 protein requires its effector domain. The NS1 effector domain functionally interacts with the cellular 30 kDa subunit of cleavage and polyadenylation specific factor 4, an essential component of the 3' end processing machinery of cellular pre-mRNAs. In influenza virus-infected cells, the NS1 protein is physically associated with cleavage and polyadenylation specific factor 4, 30kD subunit. Binding of the NS1 protein to the 30 kDa protein in vitro prevents CPSF binding to the RNA substrate and inhibits 3' end cleavage and polyadenylation of host pre-mRNAs. Thus the NS1 protein selectively inhibits the nuclear export of cellular, and not viral, mRNAs. Multiple alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":99438922,"end":99457371,"strand":1,"description":"cleavage and polyadenylation specific factor 4 [Source:HGNC Symbol;Acc:HGNC:2327]"}, {"versioned_ensembl_gene_id":"ENSG00000279334.1","gene_symbol":"AC073592.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124561869,"end":124562283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164742.14","gene_symbol":"ADCY1","gene_name":"adenylate cyclase 1 [Source:HGNC Symbol;Acc:HGNC:232]","synonyms":"DFNB44,AC1","biotype":"protein_coding","ncbi_id":"107","summary":"This gene encodes a member of the of adenylate cyclase gene family that is primarily expressed in the brain. This protein is regulated by calcium/calmodulin concentration and may be involved in brain development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":45574140,"end":45723116,"strand":1,"description":"adenylate cyclase 1 [Source:HGNC Symbol;Acc:HGNC:232]"}, {"versioned_ensembl_gene_id":"ENSG00000279071.1","gene_symbol":"AC073592.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124537844,"end":124539677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229598.1","gene_symbol":"PRDX3P1","gene_name":"peroxiredoxin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39264]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419031","summary":null,"start":38722743,"end":38723505,"strand":-1,"description":"peroxiredoxin 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39264]"}, {"versioned_ensembl_gene_id":"ENSG00000111275.12","gene_symbol":"ALDH2","gene_name":"aldehyde dehydrogenase 2 family (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:404]","synonyms":null,"biotype":"protein_coding","ncbi_id":"217","summary":"This protein belongs to the aldehyde dehydrogenase family of proteins. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. Two major liver isoforms of aldehyde dehydrogenase, cytosolic and mitochondrial, can be distinguished by their electrophoretic mobilities, kinetic properties, and subcellular localizations. Most Caucasians have two major isozymes, while approximately 50% of East Asians have the cytosolic isozyme but not the mitochondrial isozyme. A remarkably higher frequency of acute alcohol intoxication among East Asians than among Caucasians could be related to the absence of a catalytically active form of the mitochondrial isozyme. The increased exposure to acetaldehyde in individuals with the catalytically inactive form may also confer greater susceptibility to many types of cancer. This gene encodes a mitochondrial isoform, which has a low Km for acetaldehydes, and is localized in mitochondrial matrix. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Nov 2016]","start":111766887,"end":111817529,"strand":1,"description":"aldehyde dehydrogenase 2 family (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:404]"}, {"versioned_ensembl_gene_id":"ENSG00000242119.1","gene_symbol":"AC117454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151499639,"end":151499806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197364.6","gene_symbol":"S100A7L2","gene_name":"S100 calcium binding protein A7 like 2 [Source:HGNC Symbol;Acc:HGNC:21655]","synonyms":"s100a7b","biotype":"protein_coding","ncbi_id":"645922","summary":"This locus is currently categorized as a non-transcribed pseudogene, but the locus type of this gene is unclear since it does contain an intact CDS. This locus lacks evidence indicating that it is transcribed, and very little of the upstream regions found in other family members are present at this locus. [provided by RefSeq, May 2018]","start":153437058,"end":153439949,"strand":-1,"description":"S100 calcium binding protein A7 like 2 [Source:HGNC Symbol;Acc:HGNC:21655]"}, {"versioned_ensembl_gene_id":"ENSG00000225537.1","gene_symbol":"AC073325.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45460712,"end":45542182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124749.16","gene_symbol":"COL21A1","gene_name":"collagen type XXI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:17025]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81578","summary":"This gene encodes the alpha chain of type XXI collagen, a member of the FACIT (fibril-associated collagens with interrupted helices) collagen family. Type XXI collagen is localized to tissues containing type I collagen and maintains the integrity of the extracellular matrix. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":56056590,"end":56394094,"strand":-1,"description":"collagen type XXI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:17025]"}, {"versioned_ensembl_gene_id":"ENSG00000227602.1","gene_symbol":"AL031779.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56331788,"end":56332117,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260861.6","gene_symbol":"AL049634.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1540144,"end":1620009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242324.1","gene_symbol":"AL049634.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":1516759,"end":1557653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173269.13","gene_symbol":"MMRN2","gene_name":"multimerin 2 [Source:HGNC Symbol;Acc:HGNC:19888]","synonyms":"FLJ13465,EndoGlyx-1,EMILIN3","biotype":"protein_coding","ncbi_id":"79812","summary":"This gene encodes a protein belonging to the member of elastin microfibril interface-located (EMILIN) protein family. This family member is an extracellular matrix glycoprotein that can interfere with tumor angiogenesis and growth. It serves as a transforming growth factor beta antagonist and can interfere with the VEGF-A/VEGFR2 pathway. A related pseudogene has been identified on chromosome 6. [provided by RefSeq, Aug 2012]","start":86935540,"end":86969481,"strand":-1,"description":"multimerin 2 [Source:HGNC Symbol;Acc:HGNC:19888]"}, {"versioned_ensembl_gene_id":"ENSG00000237864.1","gene_symbol":"LINC00322","gene_name":"long intergenic non-protein coding RNA 322 [Source:HGNC Symbol;Acc:HGNC:33698]","synonyms":"NCRNA00322,FLJ16545,C21orf136","biotype":"lincRNA","ncbi_id":"100126693","summary":null,"start":43322417,"end":43332039,"strand":-1,"description":"long intergenic non-protein coding RNA 322 [Source:HGNC Symbol;Acc:HGNC:33698]"}, {"versioned_ensembl_gene_id":"ENSG00000233133.1","gene_symbol":"AC104451.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17706058,"end":17706233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260974.1","gene_symbol":"AC138907.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32675037,"end":32678831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270617.1","gene_symbol":"URGCP-MRPS24","gene_name":"URGCP-MRPS24 readthrough [Source:HGNC Symbol;Acc:HGNC:49188]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534592","summary":"This locus represents naturally occurring read-through transcription between the neighboring URGCP (upregulator of cell proliferation) and MRPS24 (mitochondrial ribosomal protein S24) genes on chromosome 7. The read-through transcript is predicted to encode a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to a frameshift relative to the downstream gene. [provided by RefSeq, Mar 2011]","start":43866558,"end":43906589,"strand":-1,"description":"URGCP-MRPS24 readthrough [Source:HGNC Symbol;Acc:HGNC:49188]"}, {"versioned_ensembl_gene_id":"ENSG00000167196.13","gene_symbol":"FBXO22","gene_name":"F-box protein 22 [Source:HGNC Symbol;Acc:HGNC:13593]","synonyms":"FISTC1,FBX22","biotype":"protein_coding","ncbi_id":"26263","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and, as a transcriptional target of the tumor protein p53, is thought to be involved in degradation of specific proteins in response to p53 induction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":75903859,"end":75942510,"strand":1,"description":"F-box protein 22 [Source:HGNC Symbol;Acc:HGNC:13593]"}, {"versioned_ensembl_gene_id":"ENSG00000025708.13","gene_symbol":"TYMP","gene_name":"thymidine phosphorylase [Source:HGNC Symbol;Acc:HGNC:3148]","synonyms":"MNGIE,ECGF1","biotype":"protein_coding","ncbi_id":"1890","summary":"This gene encodes an angiogenic factor which promotes angiogenesis in vivo and stimulates the in vitro growth of a variety of endothelial cells. It has a highly restricted target cell specificity acting only on endothelial cells. Mutations in this gene have been associated with mitochondrial neurogastrointestinal encephalomyopathy. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2012]","start":50525752,"end":50530056,"strand":-1,"description":"thymidine phosphorylase [Source:HGNC Symbol;Acc:HGNC:3148]"}, {"versioned_ensembl_gene_id":"ENSG00000075292.18","gene_symbol":"ZNF638","gene_name":"zinc finger protein 638 [Source:HGNC Symbol;Acc:HGNC:17894]","synonyms":"Zfp638,ZFML,NP220,MGC26130","biotype":"protein_coding","ncbi_id":"27332","summary":"The protein encoded by this gene is a nucleoplasmic protein. It binds cytidine-rich sequences in double-stranded DNA. This protein has three types of domains: MH1, MH2 (repeated three times) and MH3. It is associated with packaging, transferring, or processing transcripts. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":71276561,"end":71435069,"strand":1,"description":"zinc finger protein 638 [Source:HGNC Symbol;Acc:HGNC:17894]"}, {"versioned_ensembl_gene_id":"ENSG00000284194.1","gene_symbol":"SCO2","gene_name":"SCO2, cytochrome c oxidase assembly protein [Source:NCBI gene;Acc:9997]","synonyms":"MYP6,CEMCOX1,SCO1L,MYP6,SCO1L","biotype":"protein_coding","ncbi_id":"9997","summary":"Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors; this gene encodes one of the COX assembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy and myopia 6. [provided by RefSeq, Oct 2014]","start":50523568,"end":50526439,"strand":-1,"description":"SCO2, cytochrome c oxidase assembly protein [Source:NCBI gene;Acc:9997]"}, {"versioned_ensembl_gene_id":"ENSG00000254526.1","gene_symbol":"AC090791.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29159956,"end":29266734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114013.15","gene_symbol":"CD86","gene_name":"CD86 molecule [Source:HGNC Symbol;Acc:HGNC:1705]","synonyms":"B7-2,CD28LG2,B7.2","biotype":"protein_coding","ncbi_id":"942","summary":"This gene encodes a type I membrane protein that is a member of the immunoglobulin superfamily. This protein is expressed by antigen-presenting cells, and it is the ligand for two proteins at the cell surface of T cells, CD28 antigen and cytotoxic T-lymphocyte-associated protein 4. Binding of this protein with CD28 antigen is a costimulatory signal for activation of the T-cell. Binding of this protein with cytotoxic T-lymphocyte-associated protein 4 negatively regulates T-cell activation and diminishes the immune response. Alternative splicing results in several transcript variants encoding different isoforms.[provided by RefSeq, May 2011]","start":122055366,"end":122121139,"strand":1,"description":"CD86 molecule [Source:HGNC Symbol;Acc:HGNC:1705]"}, {"versioned_ensembl_gene_id":"ENSG00000130489.14","gene_symbol":"SCO2","gene_name":"SCO2, cytochrome c oxidase assembly protein [Source:HGNC Symbol;Acc:HGNC:10604]","synonyms":"MYP6,CEMCOX1,SCO1L,MYP6,SCO1L","biotype":"protein_coding","ncbi_id":"9997","summary":"Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors; this gene encodes one of the COX assembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy and myopia 6. [provided by RefSeq, Oct 2014]","start":50523568,"end":50525606,"strand":-1,"description":"SCO2, cytochrome c oxidase assembly protein [Source:HGNC Symbol;Acc:HGNC:10604]"}, {"versioned_ensembl_gene_id":"ENSG00000229969.1","gene_symbol":"AL136982.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87009785,"end":87015782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266541.1","gene_symbol":"AP001381.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9587386,"end":9590182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187607.15","gene_symbol":"ZNF286A","gene_name":"zinc finger protein 286A [Source:HGNC Symbol;Acc:HGNC:13501]","synonyms":"ZNF286,KIAA1874","biotype":"protein_coding","ncbi_id":"57335","summary":null,"start":15699577,"end":15720787,"strand":1,"description":"zinc finger protein 286A [Source:HGNC Symbol;Acc:HGNC:13501]"}, {"versioned_ensembl_gene_id":"ENSG00000261350.1","gene_symbol":"AC018558.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35491174,"end":35492395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130429.12","gene_symbol":"ARPC1B","gene_name":"actin related protein 2/3 complex subunit 1B [Source:HGNC Symbol;Acc:HGNC:704]","synonyms":"p41-ARC,p40-ARC,ARC41","biotype":"protein_coding","ncbi_id":"10095","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. This subunit is a member of the SOP2 family of proteins and is most similar to the protein encoded by gene ARPC1A. The similarity between these two proteins suggests that they both may function as p41 subunit of the human Arp2/3 complex that has been implicated in the control of actin polymerization in cells. It is possible that the p41 subunit is involved in assembling and maintaining the structure of the Arp2/3 complex. Multiple versions of the p41 subunit may adapt the functions of the complex to different cell types or developmental stages. This protein also has a role in centrosomal homeostasis by being an activator and substrate of the Aurora A kinase. [provided by RefSeq, Mar 2011]","start":99374249,"end":99394801,"strand":1,"description":"actin related protein 2/3 complex subunit 1B [Source:HGNC Symbol;Acc:HGNC:704]"}, {"versioned_ensembl_gene_id":"ENSG00000168936.10","gene_symbol":"TMEM129","gene_name":"transmembrane protein 129 [Source:HGNC Symbol;Acc:HGNC:25137]","synonyms":"D4S2561E","biotype":"protein_coding","ncbi_id":"92305","summary":null,"start":1715952,"end":1721358,"strand":-1,"description":"transmembrane protein 129 [Source:HGNC Symbol;Acc:HGNC:25137]"}, {"versioned_ensembl_gene_id":"ENSG00000283189.2","gene_symbol":"AC104452.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":49416777,"end":49429314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234337.4","gene_symbol":"AC026462.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52655307,"end":52656045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241767.2","gene_symbol":"LINC01324","gene_name":"long intergenic non-protein coding RNA 1324 [Source:HGNC Symbol;Acc:HGNC:50530]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355289","summary":null,"start":164714095,"end":164831480,"strand":-1,"description":"long intergenic non-protein coding RNA 1324 [Source:HGNC Symbol;Acc:HGNC:50530]"}, {"versioned_ensembl_gene_id":"ENSG00000157873.17","gene_symbol":"TNFRSF14","gene_name":"TNF receptor superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11912]","synonyms":"TR2,LIGHTR,HVEM,HVEA,CD270,ATAR","biotype":"protein_coding","ncbi_id":"8764","summary":"This gene encodes a member of the TNF (tumor necrosis factor) receptor superfamily. The encoded protein functions in signal transduction pathways that activate inflammatory and inhibitory T-cell immune response. It binds herpes simplex virus (HSV) viral envelope glycoprotein D (gD), mediating its entry into cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":2555639,"end":2565382,"strand":1,"description":"TNF receptor superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11912]"}, {"versioned_ensembl_gene_id":"ENSG00000257141.1","gene_symbol":"AC126177.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107832858,"end":107835030,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144136.10","gene_symbol":"SLC20A1","gene_name":"solute carrier family 20 member 1 [Source:HGNC Symbol;Acc:HGNC:10946]","synonyms":"PiT-1,GLVR1,Glvr-1","biotype":"protein_coding","ncbi_id":"6574","summary":"The protein encoded by this gene is a sodium-phosphate symporter that absorbs phosphate from interstitial fluid for use in cellular functions such as metabolism, signal transduction, and nucleic acid and lipid synthesis. The encoded protein is also a retroviral receptor, causing human cells to be susceptible to infection by gibbon ape leukemia virus, simian sarcoma-associated virus, feline leukemia virus subgroup B, and 10A1 murine leukemia virus.[provided by RefSeq, Mar 2011]","start":112645857,"end":112663827,"strand":1,"description":"solute carrier family 20 member 1 [Source:HGNC Symbol;Acc:HGNC:10946]"}, {"versioned_ensembl_gene_id":"ENSG00000187855.5","gene_symbol":"ASCL4","gene_name":"achaete-scute family bHLH transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:24311]","synonyms":"HASH4,bHLHa44","biotype":"protein_coding","ncbi_id":"121549","summary":"Basic helix-loop-helix transcription factors, such as ASCL4, are essential for the determination of cell fate and the development and differentiation of numerous tissues (Jonsson et al., 2004 [PubMed 15475265]).[supplied by OMIM, Mar 2008]","start":107774385,"end":107776644,"strand":1,"description":"achaete-scute family bHLH transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:24311]"}, {"versioned_ensembl_gene_id":"ENSG00000206467.6","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587257,"end":29588840,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000049759.17","gene_symbol":"NEDD4L","gene_name":"neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:7728]","synonyms":"RSP5,NEDD4-2,KIAA0439","biotype":"protein_coding","ncbi_id":"23327","summary":"This gene encodes a member of the Nedd4 family of HECT domain E3 ubiquitin ligases. HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates, thus targeting specific proteins for lysosomal degradation. The encoded protein mediates the ubiquitination of multiple target substrates and plays a critical role in epithelial sodium transport by regulating the cell surface expression of the epithelial sodium channel, ENaC. Single nucleotide polymorphisms in this gene may be associated with essential hypertension. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":58044367,"end":58401540,"strand":1,"description":"neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:7728]"}, {"versioned_ensembl_gene_id":"ENSG00000143546.9","gene_symbol":"S100A8","gene_name":"S100 calcium binding protein A8 [Source:HGNC Symbol;Acc:HGNC:10498]","synonyms":"P8,MRP8,CGLA,CFAG,CAGA,60B8AG","biotype":"protein_coding","ncbi_id":"6279","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in the inhibition of casein kinase and as a cytokine. Altered expression of this protein is associated with the disease cystic fibrosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":153390032,"end":153391188,"strand":-1,"description":"S100 calcium binding protein A8 [Source:HGNC Symbol;Acc:HGNC:10498]"}, {"versioned_ensembl_gene_id":"ENSG00000283680.1","gene_symbol":"AC135068.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21595580,"end":21596510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155256.17","gene_symbol":"ZFYVE27","gene_name":"zinc finger FYVE-type containing 27 [Source:HGNC Symbol;Acc:HGNC:26559]","synonyms":"SPG33,FLJ32919","biotype":"protein_coding","ncbi_id":"118813","summary":"This gene encodes a protein with several transmembrane domains, a Rab11-binding domain and a lipid-binding FYVE finger domain. The encoded protein appears to promote neurite formation. A mutation in this gene has been reported to be associated with hereditary spastic paraplegia, however the pathogenicity of the mutation, which may simply represent a polymorphism, is unclear. [provided by RefSeq, Mar 2010]","start":97737121,"end":97760907,"strand":1,"description":"zinc finger FYVE-type containing 27 [Source:HGNC Symbol;Acc:HGNC:26559]"}, {"versioned_ensembl_gene_id":"ENSG00000236445.4","gene_symbol":"LINC00608","gene_name":"long intergenic non-protein coding RNA 608 [Source:HGNC Symbol;Acc:HGNC:27179]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"151300","summary":null,"start":218975393,"end":218989940,"strand":1,"description":"long intergenic non-protein coding RNA 608 [Source:HGNC Symbol;Acc:HGNC:27179]"}, {"versioned_ensembl_gene_id":"ENSG00000171450.5","gene_symbol":"CDK5R2","gene_name":"cyclin dependent kinase 5 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:1776]","synonyms":"p39nck5ai,P39,NCK5AI","biotype":"protein_coding","ncbi_id":"8941","summary":"The protein encoded by this gene is a neuron-specific activator of CDK5 kinase. It associates with CDK5 to form an active kinase. This protein and neuron-specific CDK5 activator CDK5R1/p39NCK5A both share limited similarity to cyclins, and thus may define a distinct family of cyclin-dependent kinase activating proteins. [provided by RefSeq, Jul 2008]","start":218959655,"end":218962162,"strand":1,"description":"cyclin dependent kinase 5 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:1776]"}, {"versioned_ensembl_gene_id":"ENSG00000228135.1","gene_symbol":"LINC01494","gene_name":"long intergenic non-protein coding RNA 1494 [Source:HGNC Symbol;Acc:HGNC:51152]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928537","summary":null,"start":218900811,"end":218930636,"strand":-1,"description":"long intergenic non-protein coding RNA 1494 [Source:HGNC Symbol;Acc:HGNC:51152]"}, {"versioned_ensembl_gene_id":"ENSG00000225713.5","gene_symbol":"RPL30P1","gene_name":"ribosomal protein L30 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270975","summary":null,"start":174090136,"end":174090474,"strand":-1,"description":"ribosomal protein L30 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36642]"}, {"versioned_ensembl_gene_id":"ENSG00000224977.1","gene_symbol":"AL121983.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174022509,"end":174022985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271730.1","gene_symbol":"AL390208.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108998482,"end":108999125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258034.1","gene_symbol":"AC012157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":115961187,"end":115962733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185674.9","gene_symbol":"LYG2","gene_name":"lysozyme g2 [Source:HGNC Symbol;Acc:HGNC:29615]","synonyms":"LYGH","biotype":"protein_coding","ncbi_id":"254773","summary":"The protein encoded by this gene contains a SLT domain, a protein domain present in bacterial lytic transglycosylase (SLT) and in eukaryotic lysozymes (GEWL). SLT domain catalyzes the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyglucosamine (GlcNAc). [provided by RefSeq, Jul 2008]","start":99242246,"end":99255282,"strand":-1,"description":"lysozyme g2 [Source:HGNC Symbol;Acc:HGNC:29615]"}, {"versioned_ensembl_gene_id":"ENSG00000237429.1","gene_symbol":"BX293535.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27525805,"end":27530561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102021.10","gene_symbol":"LUZP4","gene_name":"leucine zipper protein 4 [Source:HGNC Symbol;Acc:HGNC:24971]","synonyms":"HOM-TES-85,CT28,CT-8","biotype":"protein_coding","ncbi_id":"51213","summary":"This gene encodes a leucine-zipper protein that was first defined as a cancer testis antigens. The encoded protein is an RNA binding protein that interacts with the mRNA export receptor nuclear RNA export factor 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":115289727,"end":115307556,"strand":1,"description":"leucine zipper protein 4 [Source:HGNC Symbol;Acc:HGNC:24971]"}, {"versioned_ensembl_gene_id":"ENSG00000211653.2","gene_symbol":"IGLV1-40","gene_name":"immunoglobulin lambda variable 1-40 [Source:HGNC Symbol;Acc:HGNC:5877]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28825","summary":null,"start":22409766,"end":22410282,"strand":1,"description":"immunoglobulin lambda variable 1-40 [Source:HGNC Symbol;Acc:HGNC:5877]"}, {"versioned_ensembl_gene_id":"ENSG00000135870.11","gene_symbol":"RC3H1","gene_name":"ring finger and CCCH-type domains 1 [Source:HGNC Symbol;Acc:HGNC:29434]","synonyms":"RP5-1198E17.5,roquin,RNF198,KIAA2025","biotype":"protein_coding","ncbi_id":"149041","summary":"This gene encodes a protein containing RING-type and C3H1-type zinc finger motifs. The encoded protein recognizes and binds to a constitutive decay element (CDE) in the 3' UTR of mRNAs, leading to mRNA deadenylation and degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":173931214,"end":174022297,"strand":-1,"description":"ring finger and CCCH-type domains 1 [Source:HGNC Symbol;Acc:HGNC:29434]"}, {"versioned_ensembl_gene_id":"ENSG00000234345.2","gene_symbol":"AC234782.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103910305,"end":103911352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175387.15","gene_symbol":"SMAD2","gene_name":"SMAD family member 2 [Source:HGNC Symbol;Acc:HGNC:6768]","synonyms":"JV18-1,MADR2,MADH2","biotype":"protein_coding","ncbi_id":"4087","summary":"The protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signal of the transforming growth factor (TGF)-beta, and thus regulates multiple cellular processes, such as cell proliferation, apoptosis, and differentiation. This protein is recruited to the TGF-beta receptors through its interaction with the SMAD anchor for receptor activation (SARA) protein. In response to TGF-beta signal, this protein is phosphorylated by the TGF-beta receptors. The phosphorylation induces the dissociation of this protein with SARA and the association with the family member SMAD4. The association with SMAD4 is important for the translocation of this protein into the nucleus, where it binds to target promoters and forms a transcription repressor complex with other cofactors. This protein can also be phosphorylated by activin type 1 receptor kinase, and mediates the signal from the activin. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2012]","start":47808957,"end":47931146,"strand":-1,"description":"SMAD family member 2 [Source:HGNC Symbol;Acc:HGNC:6768]"}, {"versioned_ensembl_gene_id":"ENSG00000231787.4","gene_symbol":"AC234782.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103904322,"end":103904754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261299.1","gene_symbol":"C2orf69P3","gene_name":"chromosome 2 open reading frame 69 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131279","summary":null,"start":35425364,"end":35426483,"strand":1,"description":"chromosome 2 open reading frame 69 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51802]"}, {"versioned_ensembl_gene_id":"ENSG00000136367.13","gene_symbol":"ZFHX2","gene_name":"zinc finger homeobox 2 [Source:HGNC Symbol;Acc:HGNC:20152]","synonyms":"ZNF409,ZFH-5,KIAA1762,KIAA1056","biotype":"protein_coding","ncbi_id":"85446","summary":null,"start":23520855,"end":23556192,"strand":-1,"description":"zinc finger homeobox 2 [Source:HGNC Symbol;Acc:HGNC:20152]"}, {"versioned_ensembl_gene_id":"ENSG00000260812.1","gene_symbol":"RARRES2P7","gene_name":"retinoic acid receptor responder 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48709]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481660","summary":null,"start":35414279,"end":35414747,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48709]"}, {"versioned_ensembl_gene_id":"ENSG00000232879.2","gene_symbol":"AL591806.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161034834,"end":161035006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224426.1","gene_symbol":"SLC31A1P1","gene_name":"solute carrier family 31 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17124]","synonyms":"SLC31A1P,CTR1psi","biotype":"processed_pseudogene","ncbi_id":"117151","summary":null,"start":172603440,"end":172604006,"strand":-1,"description":"solute carrier family 31 member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17124]"}, {"versioned_ensembl_gene_id":"ENSG00000146757.13","gene_symbol":"ZNF92","gene_name":"zinc finger protein 92 [Source:HGNC Symbol;Acc:HGNC:13168]","synonyms":"TF12,HPF12","biotype":"protein_coding","ncbi_id":"168374","summary":null,"start":65373799,"end":65401135,"strand":1,"description":"zinc finger protein 92 [Source:HGNC Symbol;Acc:HGNC:13168]"}, {"versioned_ensembl_gene_id":"ENSG00000280784.1","gene_symbol":"AL121956.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":166229334,"end":166229554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274659.1","gene_symbol":"LINC02371","gene_name":"long intergenic non-protein coding RNA 2371 [Source:HGNC Symbol;Acc:HGNC:53293]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984539","summary":null,"start":2740093,"end":2742855,"strand":1,"description":"long intergenic non-protein coding RNA 2371 [Source:HGNC Symbol;Acc:HGNC:53293]"}, {"versioned_ensembl_gene_id":"ENSG00000256150.2","gene_symbol":"ITFG2-AS1","gene_name":"ITFG2 antisense RNA 1 [Source:NCBI gene;Acc:283440]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283440","summary":null,"start":2695765,"end":2812902,"strand":-1,"description":"ITFG2 antisense RNA 1 [Source:NCBI gene;Acc:283440]"}, {"versioned_ensembl_gene_id":"ENSG00000277222.4","gene_symbol":"BTBD7","gene_name":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]","synonyms":"FUP1,FLJ10648","biotype":"protein_coding","ncbi_id":"55727","summary":null,"start":93237550,"end":93333092,"strand":-1,"description":"BTB domain containing 7 [Source:HGNC Symbol;Acc:HGNC:18269]"}, {"versioned_ensembl_gene_id":"ENSG00000281292.1","gene_symbol":"AL132838.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93244010,"end":93244323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236741.4","gene_symbol":"Z98751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171762074,"end":171762524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149782.11","gene_symbol":"PLCB3","gene_name":"phospholipase C beta 3 [Source:HGNC Symbol;Acc:HGNC:9056]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5331","summary":"This gene encodes a member of the phosphoinositide phospholipase C beta enzyme family that catalyze the production of the secondary messengers diacylglycerol and inositol 1,4,5-triphosphate from phosphatidylinositol in G-protein-linked receptor-mediated signal transduction. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":64251523,"end":64269150,"strand":1,"description":"phospholipase C beta 3 [Source:HGNC Symbol;Acc:HGNC:9056]"}, {"versioned_ensembl_gene_id":"ENSG00000145349.16","gene_symbol":"CAMK2D","gene_name":"calcium/calmodulin dependent protein kinase II delta [Source:HGNC Symbol;Acc:HGNC:1462]","synonyms":"CAMKD","biotype":"protein_coding","ncbi_id":"817","summary":"The product of this gene belongs to the serine/threonine protein kinase family and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells, the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a delta chain. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Distinct isoforms of this chain have different expression patterns.[provided by RefSeq, Nov 2008]","start":113451032,"end":113761927,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II delta [Source:HGNC Symbol;Acc:HGNC:1462]"}, {"versioned_ensembl_gene_id":"ENSG00000086189.9","gene_symbol":"DIMT1","gene_name":"DIM1 dimethyladenosine transferase 1 homolog [Source:HGNC Symbol;Acc:HGNC:30217]","synonyms":"HSA9761,DIMT1L","biotype":"protein_coding","ncbi_id":"27292","summary":"The protein encoded by this gene is a methyltransferase that is responsible for dimethylation of adjacent adenosines near the 18S rRNA decoding site. The encoded protein is essential for ribosome biogenesis, although its catalytic activity is not involved in the process. The yeast ortholog of this protein functions in the cytoplasm while this protein functions in the nucleus. [provided by RefSeq, Jan 2017]","start":62387254,"end":62403939,"strand":-1,"description":"DIM1 dimethyladenosine transferase 1 homolog [Source:HGNC Symbol;Acc:HGNC:30217]"}, {"versioned_ensembl_gene_id":"ENSG00000260311.1","gene_symbol":"AC138907.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32663925,"end":32666533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142459.8","gene_symbol":"EVI5L","gene_name":"ecotropic viral integration site 5 like [Source:HGNC Symbol;Acc:HGNC:30464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115704","summary":null,"start":7830233,"end":7864976,"strand":1,"description":"ecotropic viral integration site 5 like [Source:HGNC Symbol;Acc:HGNC:30464]"}, {"versioned_ensembl_gene_id":"ENSG00000277544.1","gene_symbol":"AC104073.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65290429,"end":65292776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282381.1","gene_symbol":"AC104073.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65269374,"end":65306238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257523.1","gene_symbol":"LINC02326","gene_name":"long intergenic non-protein coding RNA 2326 [Source:HGNC Symbol;Acc:HGNC:53246]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370425","summary":null,"start":28975836,"end":28978924,"strand":-1,"description":"long intergenic non-protein coding RNA 2326 [Source:HGNC Symbol;Acc:HGNC:53246]"}, {"versioned_ensembl_gene_id":"ENSG00000166436.15","gene_symbol":"TRIM66","gene_name":"tripartite motif containing 66 [Source:HGNC Symbol;Acc:HGNC:29005]","synonyms":"KIAA0298,TIF1D,C11orf29","biotype":"protein_coding","ncbi_id":"9866","summary":null,"start":8612037,"end":8671866,"strand":-1,"description":"tripartite motif containing 66 [Source:HGNC Symbol;Acc:HGNC:29005]"}, {"versioned_ensembl_gene_id":"ENSG00000254343.2","gene_symbol":"AC091563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120052180,"end":120056201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147432.6","gene_symbol":"CHRNB3","gene_name":"cholinergic receptor nicotinic beta 3 subunit [Source:HGNC Symbol;Acc:HGNC:1963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1142","summary":"The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are (hetero)pentamers composed of homologous subunits. The subunits that make up the muscle and neuronal forms of nAChRs are encoded by separate genes and have different primary structure. There are several subtypes of neuronal nAChRs that vary based on which homologous subunits are arranged around the central channel. They are classified as alpha-subunits if, like muscle alpha-1 (MIM 100690), they have a pair of adjacent cysteines as part of the presumed acetylcholine binding site. Subunits lacking these cysteine residues are classified as beta-subunits (Groot Kormelink and Luyten, 1997 [PubMed 9009220]). Elliott et al. (1996) [PubMed 8906617] stated that the proposed structure for each subunit is a conserved N-terminal extracellular domain followed by 3 conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region.[supplied by OMIM, Apr 2010]","start":42697376,"end":42737407,"strand":1,"description":"cholinergic receptor nicotinic beta 3 subunit [Source:HGNC Symbol;Acc:HGNC:1963]"}, {"versioned_ensembl_gene_id":"ENSG00000270124.1","gene_symbol":"AC092127.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85580009,"end":85583571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232777.1","gene_symbol":"MRPL51P2","gene_name":"mitochondrial ribosomal protein L51 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343819","summary":null,"start":43115334,"end":43115709,"strand":-1,"description":"mitochondrial ribosomal protein L51 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29724]"}, {"versioned_ensembl_gene_id":"ENSG00000270313.1","gene_symbol":"COX6CP16","gene_name":"cytochrome c oxidase subunit 6C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49367]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481965","summary":null,"start":85278820,"end":85279035,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49367]"}, {"versioned_ensembl_gene_id":"ENSG00000278716.1","gene_symbol":"AC133540.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85489813,"end":85490831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179219.5","gene_symbol":"LINC00311","gene_name":"long intergenic non-protein coding RNA 311 [Source:HGNC Symbol;Acc:HGNC:28312]","synonyms":"TMEM148,NCRNA00311,MGC22001","biotype":"lincRNA","ncbi_id":"197196","summary":null,"start":85282958,"end":85285963,"strand":1,"description":"long intergenic non-protein coding RNA 311 [Source:HGNC Symbol;Acc:HGNC:28312]"}, {"versioned_ensembl_gene_id":"ENSG00000272387.2","gene_symbol":"AL022345.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42583241,"end":42583375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107736.19","gene_symbol":"CDH23","gene_name":"cadherin related 23 [Source:HGNC Symbol;Acc:HGNC:13733]","synonyms":"USH1D,DFNB12,CDHR23","biotype":"protein_coding","ncbi_id":"64072","summary":"This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, May 2013]","start":71396934,"end":71815947,"strand":1,"description":"cadherin related 23 [Source:HGNC Symbol;Acc:HGNC:13733]"}, {"versioned_ensembl_gene_id":"ENSG00000239497.7","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"G5b,C6orf19","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31659867,"end":31664295,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000089006.16","gene_symbol":"SNX5","gene_name":"sorting nexin 5 [Source:HGNC Symbol;Acc:HGNC:14969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27131","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein functions in endosomal sorting, the phosphoinositide-signaling pathway, and macropinocytosis. This gene may play a role in the tumorigenesis of papillary thyroid carcinoma. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013]","start":17941597,"end":17968980,"strand":-1,"description":"sorting nexin 5 [Source:HGNC Symbol;Acc:HGNC:14969]"}, {"versioned_ensembl_gene_id":"ENSG00000215206.5","gene_symbol":"TRBV24OR9-2","gene_name":"T-cell receptor beta variable 24/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12204]","synonyms":"TCRBV15O,TRBV24/OR9-2,TCRBV24S2,TCRBV15S2O","biotype":"TR_V_pseudogene","ncbi_id":"6961","summary":null,"start":33649047,"end":33649614,"strand":1,"description":"T-cell receptor beta variable 24/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12204]"}, {"versioned_ensembl_gene_id":"ENSG00000229063.2","gene_symbol":"TRBV23OR9-2","gene_name":"T-cell receptor beta variable 23/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12202]","synonyms":"TRBV23OR92,TRBV23/OR9-2,TCRBV23S2,TCRBV19S2O","biotype":"TR_V_gene","ncbi_id":"28552","summary":null,"start":33638035,"end":33638494,"strand":1,"description":"T-cell receptor beta variable 23/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12202]"}, {"versioned_ensembl_gene_id":"ENSG00000237522.1","gene_symbol":"NONOP2","gene_name":"non-POU domain containing, octamer-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271700","summary":null,"start":60936819,"end":60938049,"strand":-1,"description":"non-POU domain containing, octamer-binding pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42032]"}, {"versioned_ensembl_gene_id":"ENSG00000262349.2","gene_symbol":"AC084033.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":57935074,"end":57936175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281742.2","gene_symbol":"MCCC2","gene_name":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]","synonyms":"MCCB","biotype":"protein_coding","ncbi_id":"64087","summary":"This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018]","start":70912599,"end":70929779,"strand":1,"description":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]"}, {"versioned_ensembl_gene_id":"ENSG00000224310.1","gene_symbol":"LINC01567","gene_name":"long intergenic non-protein coding RNA 1567 [Source:HGNC Symbol;Acc:HGNC:51367]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400511","summary":null,"start":24661422,"end":24671062,"strand":-1,"description":"long intergenic non-protein coding RNA 1567 [Source:HGNC Symbol;Acc:HGNC:51367]"}, {"versioned_ensembl_gene_id":"ENSG00000106066.14","gene_symbol":"CPVL","gene_name":"carboxypeptidase, vitellogenic like [Source:HGNC Symbol;Acc:HGNC:14399]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54504","summary":"The protein encoded by this gene is a carboxypeptidase and bears strong sequence similarity to serine carboxypeptidases. Carboxypeptidases are a large class of proteases that act to cleave a single amino acid from the carboxy termini of proteins or peptides. The exact function of this protein, however, has not been determined. [provided by RefSeq, Jan 2017]","start":28995231,"end":29195451,"strand":-1,"description":"carboxypeptidase, vitellogenic like [Source:HGNC Symbol;Acc:HGNC:14399]"}, {"versioned_ensembl_gene_id":"ENSG00000261669.1","gene_symbol":"AC008731.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24803451,"end":24819739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223813.2","gene_symbol":"AC007255.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29514225,"end":29563670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237065.2","gene_symbol":"NANOGP4","gene_name":"Nanog homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23102]","synonyms":"NANOGP2","biotype":"transcribed_processed_pseudogene","ncbi_id":"414132","summary":null,"start":29212302,"end":29213214,"strand":1,"description":"Nanog homeobox pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23102]"}, {"versioned_ensembl_gene_id":"ENSG00000280268.1","gene_symbol":"AC025125.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3439923,"end":3441844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268412.2","gene_symbol":"TRMT112P6","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391358","summary":null,"start":26028208,"end":26028612,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44025]"}, {"versioned_ensembl_gene_id":"ENSG00000161955.16","gene_symbol":"TNFSF13","gene_name":"TNF superfamily member 13 [Source:HGNC Symbol;Acc:HGNC:11928]","synonyms":"CD256,APRIL","biotype":"protein_coding","ncbi_id":"8741","summary":"The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF17/BCMA, a member of the TNF receptor family. This protein and its receptor are both found to be important for B cell development. In vitro experiments suggested that this protein may be able to induce apoptosis through its interaction with other TNF receptor family proteins such as TNFRSF6/FAS and TNFRSF14/HVEM. Alternative splicing results in multiple transcript variants. Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of this gene have been identified; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010]","start":7558292,"end":7561608,"strand":1,"description":"TNF superfamily member 13 [Source:HGNC Symbol;Acc:HGNC:11928]"}, {"versioned_ensembl_gene_id":"ENSG00000123560.13","gene_symbol":"PLP1","gene_name":"proteolipid protein 1 [Source:HGNC Symbol;Acc:HGNC:9086]","synonyms":"SPG2,PLP,GPM6C","biotype":"protein_coding","ncbi_id":"5354","summary":"This gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants, including the DM20 splice variant. [provided by RefSeq, Feb 2015]","start":103773718,"end":103792619,"strand":1,"description":"proteolipid protein 1 [Source:HGNC Symbol;Acc:HGNC:9086]"}, {"versioned_ensembl_gene_id":"ENSG00000254175.1","gene_symbol":"IGLVI-42","gene_name":"immunoglobulin lambda variable (I)-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5936]","synonyms":"IGLV(I)-42","biotype":"IG_V_pseudogene","ncbi_id":"28767","summary":null,"start":22397032,"end":22397524,"strand":1,"description":"immunoglobulin lambda variable (I)-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5936]"}, {"versioned_ensembl_gene_id":"ENSG00000211652.2","gene_symbol":"IGLV7-43","gene_name":"immunoglobulin lambda variable 7-43 [Source:HGNC Symbol;Acc:HGNC:5929]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28776","summary":null,"start":22395018,"end":22395489,"strand":1,"description":"immunoglobulin lambda variable 7-43 [Source:HGNC Symbol;Acc:HGNC:5929]"}, {"versioned_ensembl_gene_id":"ENSG00000228421.2","gene_symbol":"AC005013.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28957667,"end":28959345,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275560.1","gene_symbol":"AC008115.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12718973,"end":12719521,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213237.4","gene_symbol":"AC008155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138404195,"end":138404523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099246.16","gene_symbol":"RAB18","gene_name":"RAB18, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14244]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22931","summary":"The protein encoded by this gene is a member of a family of Ras-related small GTPases that regulate membrane trafficking in organelles and transport vesicles. Knockdown studies is zebrafish suggest that this protein may have a role in eye and brain development. Mutations in this gene are associated with Warburg micro syndrome type 3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":27504174,"end":27542237,"strand":1,"description":"RAB18, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14244]"}, {"versioned_ensembl_gene_id":"ENSG00000226844.1","gene_symbol":"AL662857.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29265149,"end":29266108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257519.1","gene_symbol":"AC078880.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115263170,"end":115270596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274641.1","gene_symbol":"HIST1H2BO","gene_name":"histone cluster 1 H2B family member o [Source:HGNC Symbol;Acc:HGNC:4758]","synonyms":"H2B/n,H2B.2,H2BFN","biotype":"protein_coding","ncbi_id":"8348","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27893463,"end":27893843,"strand":1,"description":"histone cluster 1 H2B family member o [Source:HGNC Symbol;Acc:HGNC:4758]"}, {"versioned_ensembl_gene_id":"ENSG00000257958.1","gene_symbol":"AC008125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115077325,"end":115080153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242169.2","gene_symbol":"AC093789.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188349376,"end":188350024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180042.5","gene_symbol":"AC087498.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":3385930,"end":3386874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115652.14","gene_symbol":"UXS1","gene_name":"UDP-glucuronate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:17729]","synonyms":"UGD,SDR6E1,FLJ23591","biotype":"protein_coding","ncbi_id":"80146","summary":"This gene encodes an enzyme found in the perinuclear Golgi which catalyzes the synthesis of UDP-xylose used in glycosaminoglycan (GAG) synthesis on proteoglycans. The GAG chains are covalently attached to proteoglycans which participate in signaling pathways during development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":106093303,"end":106194339,"strand":-1,"description":"UDP-glucuronate decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:17729]"}, {"versioned_ensembl_gene_id":"ENSG00000180068.9","gene_symbol":"OR3A4P","gene_name":"olfactory receptor family 3 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15510]","synonyms":"OR3A4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390756","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is transcribed and contains an intact ORF, but it is predicted to be a pseudogene due to a poorly conserved 7-transmembrane domain structure. [provided by RefSeq, Sep 2008]","start":3309986,"end":3311934,"strand":1,"description":"olfactory receptor family 3 subfamily A member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15510]"}, {"versioned_ensembl_gene_id":"ENSG00000283436.1","gene_symbol":"LINC01958","gene_name":"long intergenic non-protein coding RNA 1958 [Source:HGNC Symbol;Acc:HGNC:52784]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373708","summary":null,"start":156655224,"end":156695659,"strand":1,"description":"long intergenic non-protein coding RNA 1958 [Source:HGNC Symbol;Acc:HGNC:52784]"}, {"versioned_ensembl_gene_id":"ENSG00000124383.8","gene_symbol":"MPHOSPH10","gene_name":"M-phase phosphoprotein 10 [Source:HGNC Symbol;Acc:HGNC:7213]","synonyms":"MPP10P,MPP10,CT90,PPP1R106","biotype":"protein_coding","ncbi_id":"10199","summary":"This gene encodes a protein that is phosphorylated during mitosis. The protein localizes to the nucleolus during interphase and to the chromosomes during M phase. The protein associates with the U3 small nucleolar ribonucleoprotein 60-80S complexes and may be involved in pre-rRNA processing. [provided by RefSeq, Dec 2010]","start":71130314,"end":71150101,"strand":1,"description":"M-phase phosphoprotein 10 [Source:HGNC Symbol;Acc:HGNC:7213]"}, {"versioned_ensembl_gene_id":"ENSG00000107984.9","gene_symbol":"DKK1","gene_name":"dickkopf WNT signaling pathway inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:2891]","synonyms":"SK,DKK-1","biotype":"protein_coding","ncbi_id":"22943","summary":"This gene encodes a member of the dickkopf family of proteins. Members of this family are secreted proteins characterized by two cysteine-rich domains that mediate protein-protein interactions. The encoded protein binds to the LRP6 co-receptor and inhibits beta-catenin-dependent Wnt signaling. This gene plays a role in embryonic development and may be important in bone formation in adults. Elevated expression of this gene has been observed in numerous human cancers and this protein may promote proliferation, invasion and growth in cancer cell lines. [provided by RefSeq, Sep 2017]","start":52314296,"end":52318042,"strand":1,"description":"dickkopf WNT signaling pathway inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:2891]"}, {"versioned_ensembl_gene_id":"ENSG00000227179.6","gene_symbol":"PGCP1","gene_name":"progastricsin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39503]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441897","summary":null,"start":111382860,"end":111391819,"strand":-1,"description":"progastricsin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39503]"}, {"versioned_ensembl_gene_id":"ENSG00000280989.1","gene_symbol":"LINC00581","gene_name":"long intergenic non-protein coding RNA 581 [Source:HGNC Symbol;Acc:HGNC:43840]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874531","summary":null,"start":21486061,"end":21511895,"strand":-1,"description":"long intergenic non-protein coding RNA 581 [Source:HGNC Symbol;Acc:HGNC:43840]"}, {"versioned_ensembl_gene_id":"ENSG00000227915.1","gene_symbol":"ELOCP16","gene_name":"elongin C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38152]","synonyms":"TCEB1P16","biotype":"unprocessed_pseudogene","ncbi_id":"100462878","summary":null,"start":23678504,"end":23678835,"strand":1,"description":"elongin C pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38152]"}, {"versioned_ensembl_gene_id":"ENSG00000227071.1","gene_symbol":"FOCAD-AS1","gene_name":"FOCAD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49789]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929548","summary":null,"start":20683304,"end":20684688,"strand":-1,"description":"FOCAD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49789]"}, {"versioned_ensembl_gene_id":"ENSG00000231395.1","gene_symbol":"ARL4AP4","gene_name":"ADP ribosylation factor like GTPase 4A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52373]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420471","summary":null,"start":23878981,"end":23879498,"strand":-1,"description":"ADP ribosylation factor like GTPase 4A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52373]"}, {"versioned_ensembl_gene_id":"ENSG00000224411.3","gene_symbol":"HSP90AA2P","gene_name":"heat shock protein 90 alpha family class A member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:5256]","synonyms":"HSP90ALPHA,HSP90AA2,HSPCAL3,HSPCA","biotype":"processed_pseudogene","ncbi_id":"3324","summary":"HSP90 proteins are highly conserved molecular chaperones that have key roles in signal transduction, protein folding, protein degradation, and morphologic evolution. HSP90 proteins normally associate with other cochaperones and play important roles in folding newly synthesized proteins or stabilizing and refolding denatured proteins after stress. HSP90AA2 is a cytosolic HSP90 protein. Other HSP90 proteins are found in endoplasmic reticulum (HSP90B1; MIM 191175) and mitochondria (TRAP1; MIM 606219) (Chen et al., 2005 [PubMed 16269234]). See HSP90AA1 (MIM 140571) for further information on HSP90 proteins.[supplied by OMIM, Aug 2008]","start":27888838,"end":27891033,"strand":-1,"description":"heat shock protein 90 alpha family class A member 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:5256]"}, {"versioned_ensembl_gene_id":"ENSG00000280005.1","gene_symbol":"AC079298.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154261735,"end":154262193,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000113387.11","gene_symbol":"SUB1","gene_name":"SUB1 homolog, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:19985]","synonyms":"PC4,p15,p14","biotype":"protein_coding","ncbi_id":"10923","summary":null,"start":32531633,"end":32604079,"strand":1,"description":"SUB1 homolog, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:19985]"}, {"versioned_ensembl_gene_id":"ENSG00000228151.1","gene_symbol":"AC004941.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":149398204,"end":149401456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260887.2","gene_symbol":"CASC22","gene_name":"cancer susceptibility 22 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50627]","synonyms":"TCONS_00024290,LincRNA-ENST00000515084,LINC01373","biotype":"lincRNA","ncbi_id":"283854","summary":null,"start":52258564,"end":52280638,"strand":1,"description":"cancer susceptibility 22 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50627]"}, {"versioned_ensembl_gene_id":"ENSG00000160191.17","gene_symbol":"PDE9A","gene_name":"phosphodiesterase 9A [Source:HGNC Symbol;Acc:HGNC:8795]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5152","summary":"The protein encoded by this gene catalyzes the hydrolysis of cAMP and cGMP to their corresponding monophosphates. The encoded protein plays a role in signal transduction by regulating the intracellular concentration of these cyclic nucleotides. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":42653636,"end":42775509,"strand":1,"description":"phosphodiesterase 9A [Source:HGNC Symbol;Acc:HGNC:8795]"}, {"versioned_ensembl_gene_id":"ENSG00000213530.3","gene_symbol":"MTHFD2P5","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442707","summary":null,"start":82589848,"end":82590691,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48863]"}, {"versioned_ensembl_gene_id":"ENSG00000228711.1","gene_symbol":"AC004006.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82657035,"end":82657411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131873.5","gene_symbol":"CHSY1","gene_name":"chondroitin sulfate synthase 1 [Source:HGNC Symbol;Acc:HGNC:17198]","synonyms":"CSS1,KIAA0990","biotype":"protein_coding","ncbi_id":"22856","summary":"This gene encodes a member of the chondroitin N-acetylgalactosaminyltransferase family. These enzymes possess dual glucuronyltransferase and galactosaminyltransferase activity and play critical roles in the biosynthesis of chondroitin sulfate, a glycosaminoglycan involved in many biological processes including cell proliferation and morphogenesis. Decreased expression of this gene may play a role in colorectal cancer, and mutations in this gene are a cause of temtamy preaxial brachydactyly syndrome. [provided by RefSeq, Dec 2011]","start":101175723,"end":101251932,"strand":-1,"description":"chondroitin sulfate synthase 1 [Source:HGNC Symbol;Acc:HGNC:17198]"}, {"versioned_ensembl_gene_id":"ENSG00000260943.1","gene_symbol":"LINC02555","gene_name":"long intergenic non-protein coding RNA 2555 [Source:HGNC Symbol;Acc:HGNC:53593]","synonyms":"AC079630.2","biotype":"lincRNA","ncbi_id":"101930164","summary":null,"start":40140926,"end":40142876,"strand":-1,"description":"long intergenic non-protein coding RNA 2555 [Source:HGNC Symbol;Acc:HGNC:53593]"}, {"versioned_ensembl_gene_id":"ENSG00000089820.15","gene_symbol":"ARHGAP4","gene_name":"Rho GTPase activating protein 4 [Source:HGNC Symbol;Acc:HGNC:674]","synonyms":"SrGAP4,RhoGAP4,p115,KIAA0131,C1","biotype":"protein_coding","ncbi_id":"393","summary":"This gene encodes a member of the rhoGAP family of proteins which play a role in the regulation of small GTP-binding proteins belonging to the RAS superfamily. The protein encoded by the orthologous gene in rat is localized to the Golgi complex and can redistribute to microtubules. The rat protein stimulates the activity of some Rho GTPases in vitro. Genomic deletions of this gene and a neighboring gene have been found in patients with nephrogenic diabetes insipidus. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":153907367,"end":153934999,"strand":-1,"description":"Rho GTPase activating protein 4 [Source:HGNC Symbol;Acc:HGNC:674]"}, {"versioned_ensembl_gene_id":"ENSG00000163216.6","gene_symbol":"SPRR2D","gene_name":"small proline rich protein 2D [Source:HGNC Symbol;Acc:HGNC:11264]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6703","summary":null,"start":153039725,"end":153041931,"strand":-1,"description":"small proline rich protein 2D [Source:HGNC Symbol;Acc:HGNC:11264]"}, {"versioned_ensembl_gene_id":"ENSG00000160201.11","gene_symbol":"U2AF1","gene_name":"U2 small nuclear RNA auxiliary factor 1 [Source:HGNC Symbol;Acc:HGNC:12453]","synonyms":"U2AFBP,U2AF35,RNU2AF1,RN","biotype":"protein_coding","ncbi_id":"7307","summary":"This gene belongs to the splicing factor SR family of genes. U2 auxiliary factor, comprising a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the small subunit which plays a critical role in both constitutive and enhancer-dependent RNA splicing by directly mediating interactions between the large subunit and proteins bound to the enhancers. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":43092956,"end":43107587,"strand":-1,"description":"U2 small nuclear RNA auxiliary factor 1 [Source:HGNC Symbol;Acc:HGNC:12453]"}, {"versioned_ensembl_gene_id":"ENSG00000280055.1","gene_symbol":"TMEM75","gene_name":"transmembrane protein 75 [Source:HGNC Symbol;Acc:HGNC:32295]","synonyms":"FLJ36105","biotype":"TEC","ncbi_id":"641384","summary":null,"start":127946559,"end":127948723,"strand":-1,"description":"transmembrane protein 75 [Source:HGNC Symbol;Acc:HGNC:32295]"}, {"versioned_ensembl_gene_id":"ENSG00000213997.3","gene_symbol":"PGAM1P7","gene_name":"phosphoglycerate mutase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420650","summary":null,"start":46646594,"end":46647330,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42454]"}, {"versioned_ensembl_gene_id":"ENSG00000226048.1","gene_symbol":"YBX1P8","gene_name":"Y-box binding protein 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42429]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861476","summary":null,"start":46684765,"end":46685707,"strand":-1,"description":"Y-box binding protein 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42429]"}, {"versioned_ensembl_gene_id":"ENSG00000132792.18","gene_symbol":"CTNNBL1","gene_name":"catenin beta like 1 [Source:HGNC Symbol;Acc:HGNC:15879]","synonyms":"P14L,P14,NYD-SP19,NAP,FLJ21108,C20orf33","biotype":"protein_coding","ncbi_id":"56259","summary":"The protein encoded by this gene is a component of the pre-mRNA-processing factor 19-cell division cycle 5-like (PRP19-CDC5L) protein complex, which activates pre-mRNA splicing and is an integral part of the spliceosome. The encoded protein is also a nuclear localization sequence binding protein, and binds to activation-induced deaminase and is important for antibody diversification. This gene may also be associated with the development of obesity. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Jul 2013]","start":37693955,"end":37872129,"strand":1,"description":"catenin beta like 1 [Source:HGNC Symbol;Acc:HGNC:15879]"}, {"versioned_ensembl_gene_id":"ENSG00000268297.1","gene_symbol":"CLEC4GP1","gene_name":"C-type lectin domain family 4 member G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33502]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440508","summary":null,"start":7787549,"end":7790621,"strand":1,"description":"C-type lectin domain family 4 member G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33502]"}, {"versioned_ensembl_gene_id":"ENSG00000261842.1","gene_symbol":"AC073314.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149422675,"end":149424890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262591.2","gene_symbol":"TBC1D3P7","gene_name":"TBC1 domain family member 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43569]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480773","summary":null,"start":41325648,"end":41329544,"strand":1,"description":"TBC1 domain family member 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43569]"}, {"versioned_ensembl_gene_id":"ENSG00000261582.1","gene_symbol":"AL121753.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35267885,"end":35280043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278275.1","gene_symbol":"AC103705.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128010188,"end":128010428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196453.7","gene_symbol":"ZNF777","gene_name":"zinc finger protein 777 [Source:HGNC Symbol;Acc:HGNC:22213]","synonyms":"KIAA1285","biotype":"protein_coding","ncbi_id":"27153","summary":null,"start":149431363,"end":149461123,"strand":-1,"description":"zinc finger protein 777 [Source:HGNC Symbol;Acc:HGNC:22213]"}, {"versioned_ensembl_gene_id":"ENSG00000257817.1","gene_symbol":"AC026765.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114713811,"end":114767957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184524.5","gene_symbol":"CEND1","gene_name":"cell cycle exit and neuronal differentiation 1 [Source:HGNC Symbol;Acc:HGNC:24153]","synonyms":"FLJ90066,BM88","biotype":"protein_coding","ncbi_id":"51286","summary":"The protein encoded by this gene is a neuron-specific protein. The similar protein in pig enhances neuroblastoma cell differentiation in vitro and may be involved in neuronal differentiation in vivo. Multiple pseudogenes have been reported for this gene. [provided by RefSeq, Jul 2008]","start":787104,"end":790123,"strand":-1,"description":"cell cycle exit and neuronal differentiation 1 [Source:HGNC Symbol;Acc:HGNC:24153]"}, {"versioned_ensembl_gene_id":"ENSG00000215474.7","gene_symbol":"SKOR2","gene_name":"SKI family transcriptional corepressor 2 [Source:HGNC Symbol;Acc:HGNC:32695]","synonyms":"FUSSEL18,Fussel-18,CORL2","biotype":"protein_coding","ncbi_id":"652991","summary":null,"start":47206322,"end":47251603,"strand":-1,"description":"SKI family transcriptional corepressor 2 [Source:HGNC Symbol;Acc:HGNC:32695]"}, {"versioned_ensembl_gene_id":"ENSG00000205581.10","gene_symbol":"HMGN1","gene_name":"high mobility group nucleosome binding domain 1 [Source:HGNC Symbol;Acc:HGNC:4984]","synonyms":"MGC117425,MGC104230,HMG14,FLJ31471,FLJ27265","biotype":"protein_coding","ncbi_id":"3150","summary":"The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011]","start":39342315,"end":39349647,"strand":-1,"description":"high mobility group nucleosome binding domain 1 [Source:HGNC Symbol;Acc:HGNC:4984]"}, {"versioned_ensembl_gene_id":"ENSG00000101182.14","gene_symbol":"PSMA7","gene_name":"proteasome subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:9536]","synonyms":"XAPC7,RC6-1,HSPC,C6","biotype":"protein_coding","ncbi_id":"5688","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the peptidase T1A family that functions as a 20S core alpha subunit. The encoded protein interacts with the hepatitis B virus X protein and plays a role in regulating hepatitis C virus internal ribosome entry site (IRES) activity, an activity essential for viral replication. The encoded protein also plays a role in the cellular stress response by regulating hypoxia-inducible factor-1alpha. A pseudogene of this gene is located on the long arm of chromosome 9. [provided by RefSeq, Jul 2012]","start":62136735,"end":62143440,"strand":-1,"description":"proteasome subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:9536]"}, {"versioned_ensembl_gene_id":"ENSG00000116688.16","gene_symbol":"MFN2","gene_name":"mitofusin 2 [Source:HGNC Symbol;Acc:HGNC:16877]","synonyms":"MARF,KIAA0214,CPRP1,CMT2A2","biotype":"protein_coding","ncbi_id":"9927","summary":"This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":11980181,"end":12013514,"strand":1,"description":"mitofusin 2 [Source:HGNC Symbol;Acc:HGNC:16877]"}, {"versioned_ensembl_gene_id":"ENSG00000225832.1","gene_symbol":"AL035090.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20722328,"end":20723655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145996.11","gene_symbol":"CDKAL1","gene_name":"CDK5 regulatory subunit associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:21050]","synonyms":"FLJ20342","biotype":"protein_coding","ncbi_id":"54901","summary":"The protein encoded by this gene is a member of the methylthiotransferase family. The function of this gene is not known. Genome-wide association studies have linked single nucleotide polymorphisms in an intron of this gene with susceptibilty to type 2 diabetes. [provided by RefSeq, May 2010]","start":20534457,"end":21232404,"strand":1,"description":"CDK5 regulatory subunit associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:21050]"}, {"versioned_ensembl_gene_id":"ENSG00000183624.13","gene_symbol":"HMCES","gene_name":"5-hydroxymethylcytosine binding, ES cell specific [Source:HGNC Symbol;Acc:HGNC:24446]","synonyms":"SRAPD1,DC12,C3orf37","biotype":"protein_coding","ncbi_id":"56941","summary":null,"start":129278828,"end":129306186,"strand":1,"description":"5-hydroxymethylcytosine binding, ES cell specific [Source:HGNC Symbol;Acc:HGNC:24446]"}, {"versioned_ensembl_gene_id":"ENSG00000145088.8","gene_symbol":"EAF2","gene_name":"ELL associated factor 2 [Source:HGNC Symbol;Acc:HGNC:23115]","synonyms":"U19,TRAITS,BM040","biotype":"protein_coding","ncbi_id":"55840","summary":null,"start":121835183,"end":121886526,"strand":1,"description":"ELL associated factor 2 [Source:HGNC Symbol;Acc:HGNC:23115]"}, {"versioned_ensembl_gene_id":"ENSG00000169684.13","gene_symbol":"CHRNA5","gene_name":"cholinergic receptor nicotinic alpha 5 subunit [Source:HGNC Symbol;Acc:HGNC:1959]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1138","summary":"The protein encoded by this gene is a nicotinic acetylcholine receptor subunit and a member of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. These receptors are thought to be heteropentamers composed of separate but similar subunits. Defects in this gene have been linked to susceptibility to lung cancer type 2 (LNCR2).[provided by RefSeq, Jun 2010]","start":78565520,"end":78595269,"strand":1,"description":"cholinergic receptor nicotinic alpha 5 subunit [Source:HGNC Symbol;Acc:HGNC:1959]"}, {"versioned_ensembl_gene_id":"ENSG00000234388.2","gene_symbol":"TXNP3","gene_name":"thioredoxin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49483]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171419","summary":null,"start":112363281,"end":112363581,"strand":1,"description":"thioredoxin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49483]"}, {"versioned_ensembl_gene_id":"ENSG00000137936.16","gene_symbol":"BCAR3","gene_name":"breast cancer anti-estrogen resistance 3 [Source:HGNC Symbol;Acc:HGNC:973]","synonyms":"SH2D3B,NSP2","biotype":"protein_coding","ncbi_id":"8412","summary":"Breast tumors are initially dependent on estrogens for growth and progression and can be inhibited by anti-estrogens such as tamoxifen. However, breast cancers progress to become anti-estrogen resistant. Breast cancer anti-estrogen resistance gene 3 was identified in the search for genes involved in the development of estrogen resistance. The gene encodes a component of intracellular signal transduction that causes estrogen-independent proliferation in human breast cancer cells. The protein contains a putative src homology 2 (SH2) domain, a hall mark of cellular tyrosine kinase signaling molecules, and is partly homologous to the cell division cycle protein CDC48. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":93561786,"end":93847150,"strand":-1,"description":"breast cancer anti-estrogen resistance 3 [Source:HGNC Symbol;Acc:HGNC:973]"}, {"versioned_ensembl_gene_id":"ENSG00000159200.17","gene_symbol":"RCAN1","gene_name":"regulator of calcineurin 1 [Source:HGNC Symbol;Acc:HGNC:3040]","synonyms":"DSCR1","biotype":"protein_coding","ncbi_id":"1827","summary":"The protein encoded by this gene interacts with calcineurin A and inhibits calcineurin-dependent signaling pathways, possibly affecting central nervous system development. This gene is located in the minimal candidate region for the Down syndrome phenotype, and is overexpressed in the brain of Down syndrome fetuses. Chronic overexpression of this gene may lead to neurofibrillary tangles such as those associated with Alzheimer disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":34513142,"end":34615142,"strand":-1,"description":"regulator of calcineurin 1 [Source:HGNC Symbol;Acc:HGNC:3040]"}, {"versioned_ensembl_gene_id":"ENSG00000230364.1","gene_symbol":"RPL4P3","gene_name":"ribosomal protein L4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35773]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391135","summary":null,"start":171683128,"end":171684438,"strand":-1,"description":"ribosomal protein L4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35773]"}, {"versioned_ensembl_gene_id":"ENSG00000272631.1","gene_symbol":"AC067750.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86749754,"end":86756298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230073.1","gene_symbol":"AC009947.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23523321,"end":23525369,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262226.1","gene_symbol":"AC026369.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110539,"end":115865,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182888.5","gene_symbol":"AC007685.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3717149,"end":3717600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262607.5","gene_symbol":"IQSEC3","gene_name":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]","synonyms":"MGC30156,KIAA1110","biotype":"protein_coding","ncbi_id":"440073","summary":null,"start":70780,"end":175481,"strand":1,"description":"IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:HGNC:29193]"}, {"versioned_ensembl_gene_id":"ENSG00000215540.10","gene_symbol":"RBMY2CP","gene_name":"RNA binding motif protein, Y-linked, family 2, member C pseudogene [Source:HGNC Symbol;Acc:HGNC:23260]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"140123","summary":null,"start":23537308,"end":23546942,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member C pseudogene [Source:HGNC Symbol;Acc:HGNC:23260]"}, {"versioned_ensembl_gene_id":"ENSG00000233848.1","gene_symbol":"AL513188.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20756103,"end":20800694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233927.4","gene_symbol":"RPS28","gene_name":"ribosomal protein S28 [Source:HGNC Symbol;Acc:HGNC:10418]","synonyms":"S28","biotype":"protein_coding","ncbi_id":"6234","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S28E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":8321158,"end":8323340,"strand":1,"description":"ribosomal protein S28 [Source:HGNC Symbol;Acc:HGNC:10418]"}, {"versioned_ensembl_gene_id":"ENSG00000274737.1","gene_symbol":"AC004466.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47817451,"end":47817966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211584.13","gene_symbol":"SLC48A1","gene_name":"solute carrier family 48 member 1 [Source:HGNC Symbol;Acc:HGNC:26035]","synonyms":"HRG1,hHRG-1,FLJ20489","biotype":"protein_coding","ncbi_id":"55652","summary":null,"start":47753916,"end":47782753,"strand":1,"description":"solute carrier family 48 member 1 [Source:HGNC Symbol;Acc:HGNC:26035]"}, {"versioned_ensembl_gene_id":"ENSG00000236647.1","gene_symbol":"AC009947.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23549809,"end":23551385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174348.13","gene_symbol":"PODN","gene_name":"podocan [Source:HGNC Symbol;Acc:HGNC:23174]","synonyms":"SLRR5A,PODOCAN,PCAN,MGC24995","biotype":"protein_coding","ncbi_id":"127435","summary":"The protein encoded by this gene is a member of the small leucine-rich repeat protein family and contains an amino terminal CX3CXCX7C cysteine-rich cluster followed by a leucine-rich repeat domain. Studies suggest that this protein could function to inhibit smooth muscle cell proliferation and migration following arterial injury. [provided by RefSeq, Jul 2016]","start":53062052,"end":53085502,"strand":1,"description":"podocan [Source:HGNC Symbol;Acc:HGNC:23174]"}, {"versioned_ensembl_gene_id":"ENSG00000228834.1","gene_symbol":"AL445189.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108907615,"end":108907873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230290.1","gene_symbol":"ARMC2-AS1","gene_name":"ARMC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41008]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929716","summary":null,"start":108922976,"end":108924103,"strand":-1,"description":"ARMC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41008]"}, {"versioned_ensembl_gene_id":"ENSG00000118690.12","gene_symbol":"ARMC2","gene_name":"armadillo repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:23045]","synonyms":"DKFZp434P0714,bA787I22.1","biotype":"protein_coding","ncbi_id":"84071","summary":null,"start":108848416,"end":108974472,"strand":1,"description":"armadillo repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:23045]"}, {"versioned_ensembl_gene_id":"ENSG00000231931.1","gene_symbol":"AC024082.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138060056,"end":138060293,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080644.15","gene_symbol":"CHRNA3","gene_name":"cholinergic receptor nicotinic alpha 3 subunit [Source:HGNC Symbol;Acc:HGNC:1957]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1136","summary":"This locus encodes a member of the nicotinic acetylcholine receptor family of proteins. Members of this family of proteins form pentameric complexes comprised of both alpha and beta subunits. This locus encodes an alpha-type subunit, as it contains characteristic adjacent cysteine residues. The encoded protein is a ligand-gated ion channel that likely plays a role in neurotransmission. Polymorphisms in this gene have been associated with an increased risk of smoking initiation and an increased susceptibility to lung cancer. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2009]","start":78593052,"end":78621295,"strand":-1,"description":"cholinergic receptor nicotinic alpha 3 subunit [Source:HGNC Symbol;Acc:HGNC:1957]"}, {"versioned_ensembl_gene_id":"ENSG00000234639.1","gene_symbol":"AC009263.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138022458,"end":138024339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255825.1","gene_symbol":"AC006205.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":590633,"end":591269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122787.14","gene_symbol":"AKR1D1","gene_name":"aldo-keto reductase family 1 member D1 [Source:HGNC Symbol;Acc:HGNC:388]","synonyms":"SRD5B1","biotype":"protein_coding","ncbi_id":"6718","summary":"The enzyme encoded by this gene is responsible for the catalysis of the 5-beta-reduction of bile acid intermediates and steroid hormones carrying a delta(4)-3-one structure. Deficiency of this enzyme may contribute to hepatic dysfunction. Three transcript variants encoding different isoforms have been found for this gene. Other variants may be present, but their full-length natures have not been determined yet. [provided by RefSeq, Jul 2010]","start":138002324,"end":138117986,"strand":1,"description":"aldo-keto reductase family 1 member D1 [Source:HGNC Symbol;Acc:HGNC:388]"}, {"versioned_ensembl_gene_id":"ENSG00000171840.11","gene_symbol":"NINJ2","gene_name":"ninjurin 2 [Source:HGNC Symbol;Acc:HGNC:7825]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4815","summary":"The protein encoded by this gene belongs to the ninjurin (for nerve injury induced) family. It is a cell surface adhesion protein that is upregulated in Schwann cells surrounding the distal segment of injured nerve, and promotes neurite outgrowth, thus may have a role in nerve regeneration after nerve injury. [provided by RefSeq, Oct 2011]","start":564296,"end":663779,"strand":-1,"description":"ninjurin 2 [Source:HGNC Symbol;Acc:HGNC:7825]"}, {"versioned_ensembl_gene_id":"ENSG00000224970.2","gene_symbol":"AC245427.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142875836,"end":142892743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231246.1","gene_symbol":"AL445426.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112177234,"end":112360528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163251.3","gene_symbol":"FZD5","gene_name":"frizzled class receptor 5 [Source:HGNC Symbol;Acc:HGNC:4043]","synonyms":"HFZ5,DKFZP434E2135,C2orf31","biotype":"protein_coding","ncbi_id":"7855","summary":" Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD5 protein is believed to be the receptor for the Wnt5A ligand. [provided by RefSeq, Jul 2008]","start":207762586,"end":207769563,"strand":-1,"description":"frizzled class receptor 5 [Source:HGNC Symbol;Acc:HGNC:4043]"}, {"versioned_ensembl_gene_id":"ENSG00000165125.19","gene_symbol":"TRPV6","gene_name":"transient receptor potential cation channel subfamily V member 6 [Source:HGNC Symbol;Acc:HGNC:14006]","synonyms":"ECAC2,CaT1","biotype":"protein_coding","ncbi_id":"55503","summary":"This gene encodes a member of a family of multipass membrane proteins that functions as calcium channels. The encoded protein contains N-terminal ankyrin repeats, which are required for channel assembly and regulation. Translation initiation for this protein occurs at a non-AUG start codon that is decoded as methionine. This gene is situated next to a closely related gene for transient receptor potential cation channel subfamily V member 5 (TRPV5). This locus has experienced positive selection in non-African populations, resulting in several non-synonymous codon differences among individuals of different genetic backgrounds. [provided by RefSeq, Feb 2015]","start":142871203,"end":142885762,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 6 [Source:HGNC Symbol;Acc:HGNC:14006]"}, {"versioned_ensembl_gene_id":"ENSG00000198216.10","gene_symbol":"CACNA1E","gene_name":"calcium voltage-gated channel subunit alpha1 E [Source:HGNC Symbol;Acc:HGNC:1392]","synonyms":"Cav2.3,CACNL1A6,CACH6,BII","biotype":"protein_coding","ncbi_id":"777","summary":"Voltage-dependent calcium channels are multisubunit complexes consisting of alpha-1, alpha-2, beta, and delta subunits in a 1:1:1:1 ratio. These channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. This gene encodes the alpha-1E subunit of the R-type calcium channels, which belong to the 'high-voltage activated' group that maybe involved in the modulation of firing patterns of neurons important for information processing. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]","start":181413102,"end":181808084,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 E [Source:HGNC Symbol;Acc:HGNC:1392]"}, {"versioned_ensembl_gene_id":"ENSG00000274902.1","gene_symbol":"AC004241.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47731908,"end":47732351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167774.2","gene_symbol":"AC010323.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8308283,"end":8321379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280054.1","gene_symbol":"AC004241.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47728151,"end":47730598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263137.5","gene_symbol":"AC026369.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141426,"end":153184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186994.11","gene_symbol":"KANK3","gene_name":"KN motif and ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:24796]","synonyms":"FLJ46061,ANKRD47","biotype":"protein_coding","ncbi_id":"256949","summary":null,"start":8322584,"end":8343262,"strand":-1,"description":"KN motif and ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:24796]"}, {"versioned_ensembl_gene_id":"ENSG00000188906.14","gene_symbol":"LRRK2","gene_name":"leucine rich repeat kinase 2 [Source:HGNC Symbol;Acc:HGNC:18618]","synonyms":"DKFZp434H2111,ROCO2,RIPK7,PARK8,FLJ45829","biotype":"protein_coding","ncbi_id":"120892","summary":"This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008]","start":40196744,"end":40369285,"strand":1,"description":"leucine rich repeat kinase 2 [Source:HGNC Symbol;Acc:HGNC:18618]"}, {"versioned_ensembl_gene_id":"ENSG00000079337.15","gene_symbol":"RAPGEF3","gene_name":"Rap guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:16629]","synonyms":"EPAC,cAMP-GEFI,bcm910","biotype":"protein_coding","ncbi_id":"10411","summary":null,"start":47734367,"end":47771040,"strand":-1,"description":"Rap guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:16629]"}, {"versioned_ensembl_gene_id":"ENSG00000112175.7","gene_symbol":"BMP5","gene_name":"bone morphogenetic protein 5 [Source:HGNC Symbol;Acc:HGNC:1072]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone and cartilage development. Polymorphisms in this gene may be associated with osteoarthritis in human patients. This gene is differentially regulated in multiple human cancers. This gene encodes distinct protein isoforms that may be similarly proteolytically processed. [provided by RefSeq, Jul 2016]","start":55753645,"end":55875564,"strand":-1,"description":"bone morphogenetic protein 5 [Source:HGNC Symbol;Acc:HGNC:1072]"}, {"versioned_ensembl_gene_id":"ENSG00000262193.2","gene_symbol":"AC026369.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170871,"end":171722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262016.1","gene_symbol":"AC026369.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":168679,"end":170336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256020.1","gene_symbol":"AC006205.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":585865,"end":586486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178401.14","gene_symbol":"DNAJC22","gene_name":"DnaJ heat shock protein family (Hsp40) member C22 [Source:HGNC Symbol;Acc:HGNC:25802]","synonyms":"wus,FLJ13236","biotype":"protein_coding","ncbi_id":"79962","summary":null,"start":49346917,"end":49357546,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C22 [Source:HGNC Symbol;Acc:HGNC:25802]"}, {"versioned_ensembl_gene_id":"ENSG00000177406.4","gene_symbol":"AC021054.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":630891,"end":663706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213190.3","gene_symbol":"MLLT11","gene_name":"MLLT11, transcription factor 7 cofactor [Source:HGNC Symbol;Acc:HGNC:16997]","synonyms":"AF1Q","biotype":"protein_coding","ncbi_id":"10962","summary":"The gene variously symbolized ALL1, HRX, or MLL located on 11q23 has been demonstrated to be fused with a number of translocation partners in cases of leukemia. t(1;11)(q21;q23) translocations that fused the MLL gene to a gene on chromosomal band 1q21 in 2 infants with acute myelomonocytic leukemia have been demonstrated. The N-terminal portion of the MLL gene is critical for leukemogenesis in translocations involving band 11q23. This gene encodes 90 amino acids. It was found to be highly expressed in the thymus but not in peripheral lymphoid tissues. In contrast to its restricted distribution in normal hematopoietic tissue, this gene was expressed in all leukemic cell lines tested. [provided by RefSeq, Jul 2008]","start":151057758,"end":151068497,"strand":1,"description":"MLLT11, transcription factor 7 cofactor [Source:HGNC Symbol;Acc:HGNC:16997]"}, {"versioned_ensembl_gene_id":"ENSG00000225466.1","gene_symbol":"OFD1P10Y","gene_name":"OFD1 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:23882]","synonyms":"OFD1PY10,OFD1P10,OFDYP10","biotype":"unprocessed_pseudogene","ncbi_id":"386694","summary":null,"start":23581595,"end":23614640,"strand":1,"description":"OFD1 pseudogene 10, Y-linked [Source:HGNC Symbol;Acc:HGNC:23882]"}, {"versioned_ensembl_gene_id":"ENSG00000257517.1","gene_symbol":"AC026765.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114768674,"end":114771851,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205664.10","gene_symbol":"BX890604.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3817528,"end":3843857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225286.1","gene_symbol":"AC005105.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28615097,"end":28615888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253935.1","gene_symbol":"IGLVIV-53","gene_name":"immunoglobulin lambda variable (IV)-53 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5941]","synonyms":"IGLV(IV)-53","biotype":"IG_V_pseudogene","ncbi_id":"28762","summary":null,"start":22219647,"end":22220133,"strand":1,"description":"immunoglobulin lambda variable (IV)-53 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5941]"}, {"versioned_ensembl_gene_id":"ENSG00000225158.2","gene_symbol":"HSPE1P24","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480259","summary":null,"start":10895761,"end":10895998,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49343]"}, {"versioned_ensembl_gene_id":"ENSG00000235150.1","gene_symbol":"RCBTB2P1","gene_name":"RCC1 and BTB domain containing protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130253","summary":null,"start":88785600,"end":88787061,"strand":-1,"description":"RCC1 and BTB domain containing protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45167]"}, {"versioned_ensembl_gene_id":"ENSG00000143443.9","gene_symbol":"C1orf56","gene_name":"chromosome 1 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:26045]","synonyms":"MENT,FLJ20519","biotype":"protein_coding","ncbi_id":"54964","summary":"This gene is a proto-oncogene whose promoter is methylated by DNA methyltransferase 3B (DNMT3B), which represses the proto-oncogene. However, a catalytically inactive isoform of DNMT3B is overexpressed in lymphomas, leading to hypomethylation of the proto-oncogene's promoter and derepression of the proto-oncogene. [provided by RefSeq, Sep 2016]","start":151047740,"end":151051986,"strand":1,"description":"chromosome 1 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:26045]"}, {"versioned_ensembl_gene_id":"ENSG00000228050.1","gene_symbol":"TOP3BP1","gene_name":"topoisomerase (DNA) III beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11994]","synonyms":"TOP3B2","biotype":"processed_pseudogene","ncbi_id":"23751","summary":"This gene was predicted by automated computational analysis. It encodes a protein with similarity to human topoisomerase (DNA) III beta, which is thought to relax supercoiled DNA upon replication, transcription, and cell division. This gene lies in the immunoglobulin lambda gene cluster on chromosome 22q11.21. [provided by RefSeq, Jul 2008]","start":22223187,"end":22224566,"strand":-1,"description":"topoisomerase (DNA) III beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11994]"}, {"versioned_ensembl_gene_id":"ENSG00000234726.1","gene_symbol":"AC245060.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22228719,"end":22230469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169575.4","gene_symbol":"VPREB1","gene_name":"V-set pre-B cell surrogate light chain 1 [Source:HGNC Symbol;Acc:HGNC:12709]","synonyms":"VpreB,CD179A","biotype":"protein_coding","ncbi_id":"7441","summary":"The protein encoded by this gene belongs to the immunoglobulin superfamily and is expressed selectively at the early stages of B cell development, namely, in proB and early preB cells. This gene encodes the iota polypeptide chain that is associated with the Ig-mu chain to form a molecular complex which is expressed on the surface of pre-B cells. The complex is thought to regulate Ig gene rearrangements in the early steps of B-cell differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":22244675,"end":22245515,"strand":1,"description":"V-set pre-B cell surrogate light chain 1 [Source:HGNC Symbol;Acc:HGNC:12709]"}, {"versioned_ensembl_gene_id":"ENSG00000278981.1","gene_symbol":"AC079298.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154235980,"end":154237598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197622.12","gene_symbol":"CDC42SE1","gene_name":"CDC42 small effector 1 [Source:HGNC Symbol;Acc:HGNC:17719]","synonyms":"SPEC1,SCIP1","biotype":"protein_coding","ncbi_id":"56882","summary":null,"start":151050971,"end":151070325,"strand":-1,"description":"CDC42 small effector 1 [Source:HGNC Symbol;Acc:HGNC:17719]"}, {"versioned_ensembl_gene_id":"ENSG00000197410.12","gene_symbol":"DCHS2","gene_name":"dachsous cadherin-related 2 [Source:HGNC Symbol;Acc:HGNC:23111]","synonyms":"CDHR7,CDHJ,CDH27,PCDHJ,PCDH23,FLJ20047","biotype":"protein_coding","ncbi_id":"54798","summary":"This gene encodes a large protein that contains many cadherin domains and likely functions in cell adhesion. Genome-wide association studies suggest that this gene may be important in Alzheimer's disease, compressive strength index, and appendicular lean mass. [provided by RefSeq, May 2017]","start":154232037,"end":154491716,"strand":-1,"description":"dachsous cadherin-related 2 [Source:HGNC Symbol;Acc:HGNC:23111]"}, {"versioned_ensembl_gene_id":"ENSG00000218872.1","gene_symbol":"AL445189.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108856400,"end":108856737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178385.14","gene_symbol":"PLEKHM3","gene_name":"pleckstrin homology domain containing M3 [Source:HGNC Symbol;Acc:HGNC:34006]","synonyms":"PLEKHM1L,DAPR","biotype":"protein_coding","ncbi_id":"389072","summary":null,"start":207821288,"end":208025560,"strand":-1,"description":"pleckstrin homology domain containing M3 [Source:HGNC Symbol;Acc:HGNC:34006]"}, {"versioned_ensembl_gene_id":"ENSG00000175262.14","gene_symbol":"C1orf127","gene_name":"chromosome 1 open reading frame 127 [Source:HGNC Symbol;Acc:HGNC:26730]","synonyms":"FLJ37118","biotype":"protein_coding","ncbi_id":"148345","summary":null,"start":10946471,"end":10982037,"strand":-1,"description":"chromosome 1 open reading frame 127 [Source:HGNC Symbol;Acc:HGNC:26730]"}, {"versioned_ensembl_gene_id":"ENSG00000113600.10","gene_symbol":"C9","gene_name":"complement C9 [Source:HGNC Symbol;Acc:HGNC:1358]","synonyms":null,"biotype":"protein_coding","ncbi_id":"735","summary":"This gene encodes the final component of the complement system. It participates in the formation of the Membrane Attack Complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in this gene cause component C9 deficiency. [provided by RefSeq, Feb 2009]","start":39284262,"end":39424868,"strand":-1,"description":"complement C9 [Source:HGNC Symbol;Acc:HGNC:1358]"}, {"versioned_ensembl_gene_id":"ENSG00000263341.1","gene_symbol":"KRTAP17-1","gene_name":"keratin associated protein 17-1 [Source:HGNC Symbol;Acc:HGNC:18917]","synonyms":"KAP17.1","biotype":"protein_coding","ncbi_id":"83902","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41314917,"end":41315695,"strand":-1,"description":"keratin associated protein 17-1 [Source:HGNC Symbol;Acc:HGNC:18917]"}, {"versioned_ensembl_gene_id":"ENSG00000117533.14","gene_symbol":"VAMP4","gene_name":"vesicle associated membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:12645]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8674","summary":"Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. This protein may play a role in trans-Golgi network-to-endosome transport. [provided by RefSeq, Jul 2008]","start":171700160,"end":171742247,"strand":-1,"description":"vesicle associated membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:12645]"}, {"versioned_ensembl_gene_id":"ENSG00000263186.1","gene_symbol":"KRTAP16-1","gene_name":"keratin associated protein 16-1 [Source:HGNC Symbol;Acc:HGNC:18916]","synonyms":"KAP16.1","biotype":"protein_coding","ncbi_id":"100505753","summary":null,"start":41307700,"end":41309253,"strand":-1,"description":"keratin associated protein 16-1 [Source:HGNC Symbol;Acc:HGNC:18916]"}, {"versioned_ensembl_gene_id":"ENSG00000224169.1","gene_symbol":"HSFY6P","gene_name":"heat shock transcription factor, Y-linked 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:38790]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480722","summary":null,"start":23657839,"end":23659058,"strand":-1,"description":"heat shock transcription factor, Y-linked 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:38790]"}, {"versioned_ensembl_gene_id":"ENSG00000281837.1","gene_symbol":"AC217778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45371402,"end":45372057,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223407.1","gene_symbol":"USP9YP18","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38754]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480424","summary":null,"start":23659466,"end":23667822,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38754]"}, {"versioned_ensembl_gene_id":"ENSG00000225842.1","gene_symbol":"AC139712.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52474073,"end":52474411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224365.1","gene_symbol":"AC073261.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66004017,"end":66004137,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105677.11","gene_symbol":"TMEM147","gene_name":"transmembrane protein 147 [Source:HGNC Symbol;Acc:HGNC:30414]","synonyms":"NIFIE14,MGC1936","biotype":"protein_coding","ncbi_id":"10430","summary":null,"start":35545595,"end":35547526,"strand":1,"description":"transmembrane protein 147 [Source:HGNC Symbol;Acc:HGNC:30414]"}, {"versioned_ensembl_gene_id":"ENSG00000237435.9","gene_symbol":"AC099566.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95937901,"end":96022880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100884.9","gene_symbol":"CPNE6","gene_name":"copine 6 [Source:HGNC Symbol;Acc:HGNC:2319]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9362","summary":"This gene encodes a member of the copine family. Members of this family are calcium-dependent, phospholipid-binding proteins with C2 domains, two calcium- and phospholipid-binding domains. Through their domain structure and lipid binding capabilities, these proteins may play a role in membrane trafficking. This protein is thought to be brain-specific and has a domain structure of two N-terminal C2 domains and one von Willebrand factor A domain. It may have a role in synaptic plasticity. [provided by RefSeq, Jul 2013]","start":24070837,"end":24078100,"strand":1,"description":"copine 6 [Source:HGNC Symbol;Acc:HGNC:2319]"}, {"versioned_ensembl_gene_id":"ENSG00000259411.1","gene_symbol":"HNRNPA1P45","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:48775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130660","summary":null,"start":35400691,"end":35401768,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:48775]"}, {"versioned_ensembl_gene_id":"ENSG00000134389.9","gene_symbol":"CFHR5","gene_name":"complement factor H related 5 [Source:HGNC Symbol;Acc:HGNC:24668]","synonyms":"FHR5,FHR-5,CFHL5","biotype":"protein_coding","ncbi_id":"81494","summary":"This gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation. The protein encoded by this gene has nine SCRs with the first two repeats having heparin binding properties, a region within repeats 5-7 having heparin binding and C reactive protein binding properties, and the C-terminal repeats being similar to a complement component 3 b (C3b) binding domain. This protein co-localizes with C3, binds C3b in a dose-dependent manner, and is recruited to tissues damaged by C-reactive protein. Allelic variations in this gene have been associated, but not causally linked, with two different forms of kidney disease: membranoproliferative glomerulonephritis type II (MPGNII) and hemolytic uraemic syndrome (HUS). [provided by RefSeq, Jan 2010]","start":196977556,"end":197009674,"strand":1,"description":"complement factor H related 5 [Source:HGNC Symbol;Acc:HGNC:24668]"}, {"versioned_ensembl_gene_id":"ENSG00000254491.1","gene_symbol":"AC022832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13583889,"end":13584533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217930.7","gene_symbol":"PAM16","gene_name":"presequence translocase associated motor 16 homolog [Source:HGNC Symbol;Acc:HGNC:29679]","synonyms":"TIMM16,Tim16,Magmas","biotype":"protein_coding","ncbi_id":"51025","summary":"This gene encodes a mitochondrial protein involved in granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling. This protein also plays a role in the import of nuclear-encoded mitochondrial proteins into the mitochondrial matrix and may be important in reactive oxygen species (ROS) homeostasis. Mutations in this gene cause Megarbane-Dagher-Melike type spondylometaphyseal dysplasia, an early lethal skeletal dysplasia characterized by short stature, developmental delay and other skeletal abnormalities. [provided by RefSeq, May 2017]","start":4331549,"end":4355607,"strand":-1,"description":"presequence translocase associated motor 16 homolog [Source:HGNC Symbol;Acc:HGNC:29679]"}, {"versioned_ensembl_gene_id":"ENSG00000169188.4","gene_symbol":"APEX2","gene_name":"apurinic/apyrimidinic endodeoxyribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:17889]","synonyms":"ZGRF2,XTH2,APEXL2,APE2","biotype":"protein_coding","ncbi_id":"27301","summary":"Apurinic/apyrimidinic (AP) sites occur frequently in DNA molecules by spontaneous hydrolysis, by DNA damaging agents or by DNA glycosylases that remove specific abnormal bases. AP sites are pre-mutagenic lesions that can prevent normal DNA replication so the cell contains systems to identify and repair such sites. Class II AP endonucleases cleave the phosphodiester backbone 5' to the AP site. This gene encodes a protein shown to have a weak class II AP endonuclease activity. Most of the encoded protein is located in the nucleus but some is also present in mitochondria. This protein may play an important role in both nuclear and mitochondrial base excision repair. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]","start":55000357,"end":55009057,"strand":1,"description":"apurinic/apyrimidinic endodeoxyribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:17889]"}, {"versioned_ensembl_gene_id":"ENSG00000164484.11","gene_symbol":"TMEM200A","gene_name":"transmembrane protein 200A [Source:HGNC Symbol;Acc:HGNC:21075]","synonyms":"TTMC,KIAA1913","biotype":"protein_coding","ncbi_id":"114801","summary":null,"start":130365734,"end":130443063,"strand":1,"description":"transmembrane protein 200A [Source:HGNC Symbol;Acc:HGNC:21075]"}, {"versioned_ensembl_gene_id":"ENSG00000242021.2","gene_symbol":"AC112493.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27042907,"end":27176298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228933.7","gene_symbol":"AC107419.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27174920,"end":27398997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168314.17","gene_symbol":"MOBP","gene_name":"myelin-associated oligodendrocyte basic protein [Source:HGNC Symbol;Acc:HGNC:7189]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4336","summary":null,"start":39467198,"end":39529479,"strand":1,"description":"myelin-associated oligodendrocyte basic protein [Source:HGNC Symbol;Acc:HGNC:7189]"}, {"versioned_ensembl_gene_id":"ENSG00000281984.1","gene_symbol":"IGHD2-21","gene_name":"immunoglobulin heavy diversity 2-21 [Source:HGNC Symbol;Acc:HGNC:5491]","synonyms":"IGHD221","biotype":"IG_D_gene","ncbi_id":"28502","summary":null,"start":105889322,"end":105889349,"strand":-1,"description":"immunoglobulin heavy diversity 2-21 [Source:HGNC Symbol;Acc:HGNC:5491]"}, {"versioned_ensembl_gene_id":"ENSG00000116726.4","gene_symbol":"PRAMEF12","gene_name":"PRAME family member 12 [Source:HGNC Symbol;Acc:HGNC:22125]","synonyms":"OTTHUMG00000001927","biotype":"protein_coding","ncbi_id":"390999","summary":null,"start":12774841,"end":12777906,"strand":1,"description":"PRAME family member 12 [Source:HGNC Symbol;Acc:HGNC:22125]"}, {"versioned_ensembl_gene_id":"ENSG00000125820.5","gene_symbol":"NKX2-2","gene_name":"NK2 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7835]","synonyms":"NKX2B,NKX2.2","biotype":"protein_coding","ncbi_id":"4821","summary":"The protein encoded by this gene contains a homeobox domain and may be involved in the morphogenesis of the central nervous system. This gene is found on chromosome 20 near NKX2-4, and these two genes appear to be duplicated on chromosome 14 in the form of TITF1 and NKX2-8. The encoded protein is likely to be a nuclear transcription factor. [provided by RefSeq, Jul 2008]","start":21511010,"end":21514026,"strand":-1,"description":"NK2 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7835]"}, {"versioned_ensembl_gene_id":"ENSG00000227493.1","gene_symbol":"AC239367.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51030422,"end":51031357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105988.6","gene_symbol":"NHP2P1","gene_name":"NHP2 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23582]","synonyms":"NOLA2P1,bA360G10.4","biotype":"processed_pseudogene","ncbi_id":"414200","summary":null,"start":92216332,"end":92216793,"strand":1,"description":"NHP2 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23582]"}, {"versioned_ensembl_gene_id":"ENSG00000275321.1","gene_symbol":"AC010329.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20674923,"end":20696533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236599.1","gene_symbol":"ELOCP26","gene_name":"elongin C pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:38731]","synonyms":"TCEB1P26","biotype":"processed_pseudogene","ncbi_id":"101059905","summary":null,"start":18178932,"end":18179260,"strand":-1,"description":"elongin C pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:38731]"}, {"versioned_ensembl_gene_id":"ENSG00000123636.17","gene_symbol":"BAZ2B","gene_name":"bromodomain adjacent to zinc finger domain 2B [Source:HGNC Symbol;Acc:HGNC:963]","synonyms":"WALp4","biotype":"protein_coding","ncbi_id":"29994","summary":"This gene belongs to the bromodomain gene family. Members of this gene family encode proteins that are integral components of chromatin remodeling complexes. The encoded protein showed strong preference for the activating H3K14Ac mark in a histone peptide screen, suggesting a potential role in transcriptional activation. This gene may be associated with susceptibility to sudden cardiac death (SCD). [provided by RefSeq, Aug 2016]","start":159318979,"end":159616692,"strand":-1,"description":"bromodomain adjacent to zinc finger domain 2B [Source:HGNC Symbol;Acc:HGNC:963]"}, {"versioned_ensembl_gene_id":"ENSG00000225369.1","gene_symbol":"AC009506.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159462417,"end":159463256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257093.6","gene_symbol":"KIAA1147","gene_name":"KIAA1147 [Source:HGNC Symbol;Acc:HGNC:29472]","synonyms":"LCHN","biotype":"protein_coding","ncbi_id":"57189","summary":null,"start":141656728,"end":141702153,"strand":-1,"description":"KIAA1147 [Source:HGNC Symbol;Acc:HGNC:29472]"}, {"versioned_ensembl_gene_id":"ENSG00000188372.14","gene_symbol":"ZP3","gene_name":"zona pellucida glycoprotein 3 [Source:HGNC Symbol;Acc:HGNC:13189]","synonyms":"ZP3-372,ZPC,ZP3B,ZP3A,ZP3-424","biotype":"protein_coding","ncbi_id":"7784","summary":"The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed primarily of three or four glycoproteins with various functions during fertilization and preimplantation development. The protein encoded by this gene is a structural component of the zona pellucida and functions in primary binding and induction of the sperm acrosome reaction. The nascent protein contains a N-terminal signal peptide sequence, a conserved ZP domain, a C-terminal consensus furin cleavage site, and a transmembrane domain. It is hypothesized that furin cleavage results in release of the mature protein from the plasma membrane for subsequent incorporation into the zona pellucida matrix. However, the requirement for furin cleavage in this process remains controversial based on mouse studies. A variation in the last exon of this gene has previously served as the basis for an additional ZP3 locus; however, sequence and literature review reveals that there is only one full-length ZP3 locus in the human genome. Another locus encoding a bipartite transcript designated POMZP3 contains a duplication of the last four exons of ZP3, including the above described variation, and maps closely to this gene. [provided by RefSeq, Jul 2008]","start":76397518,"end":76442071,"strand":1,"description":"zona pellucida glycoprotein 3 [Source:HGNC Symbol;Acc:HGNC:13189]"}, {"versioned_ensembl_gene_id":"ENSG00000277181.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54858645,"end":54875417,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000282672.1","gene_symbol":"IGHJ1P","gene_name":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]","synonyms":"Jpsi1","biotype":"IG_J_pseudogene","ncbi_id":"28482","summary":null,"start":105866395,"end":105866449,"strand":-1,"description":"immunoglobulin heavy joining 1P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5533]"}, {"versioned_ensembl_gene_id":"ENSG00000275061.2","gene_symbol":"AC122133.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57067950,"end":57074664,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077274.8","gene_symbol":"CAPN6","gene_name":"calpain 6 [Source:HGNC Symbol;Acc:HGNC:1483]","synonyms":"CAPNX,CANPX,CalpM","biotype":"protein_coding","ncbi_id":"827","summary":"Calpains are ubiquitous, well-conserved family of calcium-dependent, cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large subunit possesses a cysteine protease domain, and both subunits possess calcium-binding domains. Calpains have been implicated in neurodegenerative processes, as their activation can be triggered by calcium influx and oxidative stress. The protein encoded by this gene is highly expressed in the placenta. Its C-terminal region lacks any homology to the calmodulin-like domain of other calpains. The protein lacks critical active site residues and thus is suggested to be proteolytically inactive. The protein may play a role in tumor formation by inhibiting apoptosis and promoting angiogenesis. [provided by RefSeq, Nov 2009]","start":111245103,"end":111270523,"strand":-1,"description":"calpain 6 [Source:HGNC Symbol;Acc:HGNC:1483]"}, {"versioned_ensembl_gene_id":"ENSG00000228307.1","gene_symbol":"OR2S1P","gene_name":"olfactory receptor family 2 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8275]","synonyms":"OST611","biotype":"unprocessed_pseudogene","ncbi_id":"392313","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":36013184,"end":36014133,"strand":1,"description":"olfactory receptor family 2 subfamily S member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8275]"}, {"versioned_ensembl_gene_id":"ENSG00000184445.11","gene_symbol":"KNTC1","gene_name":"kinetochore associated 1 [Source:HGNC Symbol;Acc:HGNC:17255]","synonyms":"ROD,KIAA0166","biotype":"protein_coding","ncbi_id":"9735","summary":"This gene encodes a protein that is one of many involved in mechanisms to ensure proper chromosome segregation during cell division. Experimental evidence indicated that the encoded protein functioned in a similar manner to that of the Drosophila rough deal protein. [provided by RefSeq, Jul 2008]","start":122527246,"end":122626396,"strand":1,"description":"kinetochore associated 1 [Source:HGNC Symbol;Acc:HGNC:17255]"}, {"versioned_ensembl_gene_id":"ENSG00000227693.1","gene_symbol":"GSTM3P1","gene_name":"glutathione S-transferase mu 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16606]","synonyms":"GSTM3P,dJ984P4.2","biotype":"processed_pseudogene","ncbi_id":"170523","summary":null,"start":21501395,"end":21501968,"strand":1,"description":"glutathione S-transferase mu 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16606]"}, {"versioned_ensembl_gene_id":"ENSG00000251189.1","gene_symbol":"AC010425.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38682070,"end":38685126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244721.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLAL,HLA92,HLA-92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30249099,"end":30256416,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000253230.8","gene_symbol":"LINC00599","gene_name":"long intergenic non-protein coding RNA 599 [Source:HGNC Symbol;Acc:HGNC:27231]","synonyms":"Rncr3","biotype":"lincRNA","ncbi_id":"157627","summary":null,"start":9900064,"end":9905366,"strand":-1,"description":"long intergenic non-protein coding RNA 599 [Source:HGNC Symbol;Acc:HGNC:27231]"}, {"versioned_ensembl_gene_id":"ENSG00000226358.1","gene_symbol":"KRT8P38","gene_name":"keratin 8 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39872]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418799","summary":null,"start":88727485,"end":88728914,"strand":1,"description":"keratin 8 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39872]"}, {"versioned_ensembl_gene_id":"ENSG00000248429.5","gene_symbol":"AC098679.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158170752,"end":158202877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264254.1","gene_symbol":"AP001496.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5310396,"end":5317664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274281.1","gene_symbol":"AC022929.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38851306,"end":38853432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185875.12","gene_symbol":"THNSL1","gene_name":"threonine synthase like 1 [Source:HGNC Symbol;Acc:HGNC:26160]","synonyms":"TSH1,FLJ22002","biotype":"protein_coding","ncbi_id":"79896","summary":null,"start":25016658,"end":25026664,"strand":1,"description":"threonine synthase like 1 [Source:HGNC Symbol;Acc:HGNC:26160]"}, {"versioned_ensembl_gene_id":"ENSG00000262038.1","gene_symbol":"AC007599.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47529190,"end":47529916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260012.1","gene_symbol":"AC007494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47262741,"end":47263500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228504.1","gene_symbol":"LINC01760","gene_name":"long intergenic non-protein coding RNA 1760 [Source:HGNC Symbol;Acc:HGNC:52549]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996630","summary":null,"start":95310928,"end":95318263,"strand":-1,"description":"long intergenic non-protein coding RNA 1760 [Source:HGNC Symbol;Acc:HGNC:52549]"}, {"versioned_ensembl_gene_id":"ENSG00000237286.1","gene_symbol":"AC004906.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2944035,"end":2947091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233146.1","gene_symbol":"BPIFB5P","gene_name":"BPI fold containing family B member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42177]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100505383","summary":null,"start":33316869,"end":33329969,"strand":1,"description":"BPI fold containing family B member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:42177]"}, {"versioned_ensembl_gene_id":"ENSG00000272702.1","gene_symbol":"AC010913.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73113018,"end":73115907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229484.1","gene_symbol":"AC243836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12527724,"end":12528420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134146.11","gene_symbol":"DPH6","gene_name":"diphthamine biosynthesis 6 [Source:HGNC Symbol;Acc:HGNC:30543]","synonyms":"MGC14798,ATPBD4","biotype":"protein_coding","ncbi_id":"89978","summary":null,"start":35217345,"end":35546193,"strand":-1,"description":"diphthamine biosynthesis 6 [Source:HGNC Symbol;Acc:HGNC:30543]"}, {"versioned_ensembl_gene_id":"ENSG00000178460.17","gene_symbol":"MCMDC2","gene_name":"minichromosome maintenance domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26368]","synonyms":"FLJ25692,C8orf45","biotype":"protein_coding","ncbi_id":"157777","summary":null,"start":66870749,"end":66922048,"strand":1,"description":"minichromosome maintenance domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26368]"}, {"versioned_ensembl_gene_id":"ENSG00000253210.1","gene_symbol":"AC040970.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141126044,"end":141129961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215158.9","gene_symbol":"AC138409.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34164698,"end":34244796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169344.15","gene_symbol":"UMOD","gene_name":"uromodulin [Source:HGNC Symbol;Acc:HGNC:12559]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7369","summary":"The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":20333052,"end":20356301,"strand":-1,"description":"uromodulin [Source:HGNC Symbol;Acc:HGNC:12559]"}, {"versioned_ensembl_gene_id":"ENSG00000176746.6","gene_symbol":"MAGEB6","gene_name":"MAGE family member B6 [Source:HGNC Symbol;Acc:HGNC:23796]","synonyms":"MAGEB6A,MAGE-B6,FLJ40242,CT3.4","biotype":"protein_coding","ncbi_id":"158809","summary":"This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is expressed in testis, and in a significant fraction of tumors of various histological types. The MAGEB genes are clustered on chromosome Xp22-p21. [provided by RefSeq, Jul 2008]","start":26192440,"end":26195646,"strand":1,"description":"MAGE family member B6 [Source:HGNC Symbol;Acc:HGNC:23796]"}, {"versioned_ensembl_gene_id":"ENSG00000213421.4","gene_symbol":"AC099670.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100586649,"end":100587431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272273.1","gene_symbol":"AL662797.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30742929,"end":30743592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225953.2","gene_symbol":"SATB2-AS1","gene_name":"SATB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26490]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"150538","summary":null,"start":199457700,"end":199476935,"strand":1,"description":"SATB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26490]"}, {"versioned_ensembl_gene_id":"ENSG00000272760.1","gene_symbol":"AC093726.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154951226,"end":154952188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157212.18","gene_symbol":"PAXIP1","gene_name":"PAX interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8624]","synonyms":"TNRC2,PTIP,PAXIP1L,CAGF29,CAGF28","biotype":"protein_coding","ncbi_id":"22976","summary":"This gene is a member of the paired box (PAX) gene family and encodes a nuclear protein with six BRCT (breast cancer carboxy-terminal) domains. This protein plays a critical role in maintaining genome stability, condensation of chromatin and progression through mitosis. [provided by RefSeq, Jul 2008]","start":154943687,"end":155003084,"strand":-1,"description":"PAX interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8624]"}, {"versioned_ensembl_gene_id":"ENSG00000232117.1","gene_symbol":"LINC00384","gene_name":"long intergenic non-protein coding RNA 384 [Source:HGNC Symbol;Acc:HGNC:42711]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102157400","summary":null,"start":30151886,"end":30159621,"strand":-1,"description":"long intergenic non-protein coding RNA 384 [Source:HGNC Symbol;Acc:HGNC:42711]"}, {"versioned_ensembl_gene_id":"ENSG00000146574.15","gene_symbol":"CCZ1B","gene_name":"CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated [Source:HGNC Symbol;Acc:HGNC:21717]","synonyms":"MGC19819,H_NH0577018.2,DKFZP586I1023,C7orf28B","biotype":"protein_coding","ncbi_id":"221960","summary":null,"start":6794134,"end":6826770,"strand":-1,"description":"CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated [Source:HGNC Symbol;Acc:HGNC:21717]"}, {"versioned_ensembl_gene_id":"ENSG00000257045.1","gene_symbol":"AC016746.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":199325310,"end":199329362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092330.15","gene_symbol":"TINF2","gene_name":"TERF1 interacting nuclear factor 2 [Source:HGNC Symbol;Acc:HGNC:11824]","synonyms":"TIN2","biotype":"protein_coding","ncbi_id":"26277","summary":"This gene encodes one of the proteins of the shelterin, or telosome, complex which protects telomeres by allowing the cell to distinguish between telomeres and regions of DNA damage. The protein encoded by this gene is a critical part of shelterin; it interacts with the three DNA-binding proteins of the shelterin complex, and it is important for assembly of the complex. Mutations in this gene cause dyskeratosis congenita (DKC), an inherited bone marrow failure syndrome. [provided by RefSeq, Mar 2010]","start":24239643,"end":24242674,"strand":-1,"description":"TERF1 interacting nuclear factor 2 [Source:HGNC Symbol;Acc:HGNC:11824]"}, {"versioned_ensembl_gene_id":"ENSG00000268173.3","gene_symbol":"AC007192.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18153158,"end":18178117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116288.12","gene_symbol":"PARK7","gene_name":"Parkinsonism associated deglycase [Source:HGNC Symbol;Acc:HGNC:16369]","synonyms":"GATD2,DJ1,DJ-1","biotype":"protein_coding","ncbi_id":"11315","summary":"The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":7954291,"end":7985505,"strand":1,"description":"Parkinsonism associated deglycase [Source:HGNC Symbol;Acc:HGNC:16369]"}, {"versioned_ensembl_gene_id":"ENSG00000129473.9","gene_symbol":"BCL2L2","gene_name":"BCL2 like 2 [Source:HGNC Symbol;Acc:HGNC:995]","synonyms":"PPP1R51,KIAA0271,BCL-W","biotype":"protein_coding","ncbi_id":"599","summary":"This gene encodes a member of the BCL-2 protein family. The proteins of this family form hetero- or homodimers and act as anti- and pro-apoptotic regulators. Expression of this gene in cells has been shown to contribute to reduced cell apoptosis under cytotoxic conditions. Studies of the related gene in mice indicated a role in the survival of NGF- and BDNF-dependent neurons. Mutation and knockout studies of the mouse gene demonstrated an essential role in adult spermatogenesis. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring downstream PABPN1 (poly(A) binding protein, nuclear 1) gene. [provided by RefSeq, Dec 2010]","start":23298790,"end":23311759,"strand":1,"description":"BCL2 like 2 [Source:HGNC Symbol;Acc:HGNC:995]"}, {"versioned_ensembl_gene_id":"ENSG00000282428.1","gene_symbol":"AC129915.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1107813,"end":1107997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103479.15","gene_symbol":"RBL2","gene_name":"RB transcriptional corepressor like 2 [Source:HGNC Symbol;Acc:HGNC:9894]","synonyms":"Rb2,p130","biotype":"protein_coding","ncbi_id":"5934","summary":null,"start":53433977,"end":53491649,"strand":1,"description":"RB transcriptional corepressor like 2 [Source:HGNC Symbol;Acc:HGNC:9894]"}, {"versioned_ensembl_gene_id":"ENSG00000090447.11","gene_symbol":"TFAP4","gene_name":"transcription factor AP-4 [Source:HGNC Symbol;Acc:HGNC:11745]","synonyms":"bHLHc41,AP-4","biotype":"protein_coding","ncbi_id":"7023","summary":"Transcription factors of the basic helix-loop-helix-zipper (bHLH-ZIP) family contain a basic domain, which is used for DNA binding, and HLH and ZIP domains, which are used for oligomerization. Transcription factor AP4 activates both viral and cellular genes by binding to the symmetrical DNA sequence CAGCTG (Mermod et al., 1988 [PubMed 2833704]; Hu et al., 1990 [PubMed 2123466]).[supplied by OMIM, Jul 2009]","start":4257186,"end":4273075,"strand":-1,"description":"transcription factor AP-4 [Source:HGNC Symbol;Acc:HGNC:11745]"}, {"versioned_ensembl_gene_id":"ENSG00000241095.1","gene_symbol":"CYP51A1P1","gene_name":"cytochrome P450 family 51 subfamily A member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20245]","synonyms":"CYP51P1","biotype":"processed_pseudogene","ncbi_id":"83528","summary":null,"start":82806515,"end":82808021,"strand":-1,"description":"cytochrome P450 family 51 subfamily A member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20245]"}, {"versioned_ensembl_gene_id":"ENSG00000240216.7","gene_symbol":"CPHL1P","gene_name":"ceruloplasmin and hephaestin-like 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31714]","synonyms":"CPHL1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"389160","summary":null,"start":149229356,"end":149291800,"strand":-1,"description":"ceruloplasmin and hephaestin-like 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31714]"}, {"versioned_ensembl_gene_id":"ENSG00000226228.1","gene_symbol":"HCG23","gene_name":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]","synonyms":"dJ1077I5.3","biotype":"processed_transcript","ncbi_id":"414764","summary":null,"start":32366008,"end":32369184,"strand":1,"description":"HLA complex group 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:19713]"}, {"versioned_ensembl_gene_id":"ENSG00000133731.9","gene_symbol":"IMPA1","gene_name":"inositol monophosphatase 1 [Source:HGNC Symbol;Acc:HGNC:6050]","synonyms":"IMPA","biotype":"protein_coding","ncbi_id":"3612","summary":"This gene encodes an enzyme that dephosphorylates myo-inositol monophosphate to generate free myo-inositol, a precursor of phosphatidylinositol, and is therefore an important modulator of intracellular signal transduction via the production of the second messengers myoinositol 1,4,5-trisphosphate and diacylglycerol. This enzyme can also use myo-inositol-1,3-diphosphate, myo-inositol-1,4-diphosphate, scyllo-inositol-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate, and 2'-AMP as substrates. This enzyme shows magnesium-dependent phosphatase activity and is inhibited by therapeutic concentrations of lithium. Inhibition of inositol monophosphate hydroylosis and subsequent depletion of inositol for phosphatidylinositol synthesis may explain the anti-manic and anti-depressive effects of lithium administered to treat bipolar disorder. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A pseudogene of this gene is also present on chromosome 8q21.13. [provided by RefSeq, Dec 2014]","start":81657961,"end":81686693,"strand":-1,"description":"inositol monophosphatase 1 [Source:HGNC Symbol;Acc:HGNC:6050]"}, {"versioned_ensembl_gene_id":"ENSG00000282472.1","gene_symbol":"AC026950.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":883198,"end":1140708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231435.1","gene_symbol":"AC011747.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8543592,"end":8575501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169249.12","gene_symbol":"ZRSR2","gene_name":"zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 [Source:HGNC Symbol;Acc:HGNC:23019]","synonyms":"URP,U2AF1L2,U2AF1-RS2,ZC3H22","biotype":"protein_coding","ncbi_id":"8233","summary":"This gene encodes an essential splicing factor. The encoded protein associates with the U2 auxiliary factor heterodimer, which is required for the recognition of a functional 3' splice site in pre-mRNA splicing, and may play a role in network interactions during spliceosome assembly. [provided by RefSeq, Jul 2008]","start":15790472,"end":15823260,"strand":1,"description":"zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 [Source:HGNC Symbol;Acc:HGNC:23019]"}, {"versioned_ensembl_gene_id":"ENSG00000198650.10","gene_symbol":"TAT","gene_name":"tyrosine aminotransferase [Source:HGNC Symbol;Acc:HGNC:11573]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6898","summary":"This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]","start":71565660,"end":71577130,"strand":-1,"description":"tyrosine aminotransferase [Source:HGNC Symbol;Acc:HGNC:11573]"}, {"versioned_ensembl_gene_id":"ENSG00000283458.1","gene_symbol":"AC011139.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39314240,"end":39328008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243064.8","gene_symbol":"ABCC13","gene_name":"ATP binding cassette subfamily C member 13 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16022]","synonyms":"ABCC13P,PRED6,C21orf73","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"150000","summary":"This gene is a member of the superfamily of genes encoding ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This family member is part of the MRP subfamily, which is involved in multi-drug resistance, but the human locus is now thought to be a pseudogene incapable of encoding a functional ABC protein. Alternative splicing results in multiple transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]","start":14236206,"end":14362754,"strand":1,"description":"ATP binding cassette subfamily C member 13 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16022]"}, {"versioned_ensembl_gene_id":"ENSG00000002933.7","gene_symbol":"TMEM176A","gene_name":"transmembrane protein 176A [Source:HGNC Symbol;Acc:HGNC:24930]","synonyms":"MS4B1,HCA112","biotype":"protein_coding","ncbi_id":"55365","summary":null,"start":150800403,"end":150805120,"strand":1,"description":"transmembrane protein 176A [Source:HGNC Symbol;Acc:HGNC:24930]"}, {"versioned_ensembl_gene_id":"ENSG00000119929.12","gene_symbol":"CUTC","gene_name":"cutC copper transporter [Source:HGNC Symbol;Acc:HGNC:24271]","synonyms":"CGI-32","biotype":"protein_coding","ncbi_id":"51076","summary":"Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008]","start":99702558,"end":99756134,"strand":1,"description":"cutC copper transporter [Source:HGNC Symbol;Acc:HGNC:24271]"}, {"versioned_ensembl_gene_id":"ENSG00000198612.10","gene_symbol":"COPS8","gene_name":"COP9 signalosome subunit 8 [Source:HGNC Symbol;Acc:HGNC:24335]","synonyms":"MGC1297,CSN8,COP9,SGN8","biotype":"protein_coding","ncbi_id":"10920","summary":"The protein encoded by this gene is one of the eight subunits of COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":237085312,"end":237100466,"strand":1,"description":"COP9 signalosome subunit 8 [Source:HGNC Symbol;Acc:HGNC:24335]"}, {"versioned_ensembl_gene_id":"ENSG00000179564.3","gene_symbol":"LSMEM2","gene_name":"leucine rich single-pass membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:26781]","synonyms":"FLJ38608,C3orf45","biotype":"protein_coding","ncbi_id":"132228","summary":null,"start":50279027,"end":50288114,"strand":1,"description":"leucine rich single-pass membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:26781]"}, {"versioned_ensembl_gene_id":"ENSG00000205903.6","gene_symbol":"ZNF316","gene_name":"zinc finger protein 316 [Source:HGNC Symbol;Acc:HGNC:13843]","synonyms":"MZF-3,ENST00000305834","biotype":"protein_coding","ncbi_id":"100131017","summary":null,"start":6637322,"end":6656432,"strand":1,"description":"zinc finger protein 316 [Source:HGNC Symbol;Acc:HGNC:13843]"}, {"versioned_ensembl_gene_id":"ENSG00000283076.1","gene_symbol":"AC015978.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17514502,"end":17516715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233299.1","gene_symbol":"HIGD1AP4","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874435","summary":null,"start":223398267,"end":223398546,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43000]"}, {"versioned_ensembl_gene_id":"ENSG00000189212.12","gene_symbol":"DPY19L2P1","gene_name":"DPY19L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22305]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"554236","summary":null,"start":35079989,"end":35186041,"strand":-1,"description":"DPY19L2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22305]"}, {"versioned_ensembl_gene_id":"ENSG00000279712.1","gene_symbol":"FP325330.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47916728,"end":47926264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261097.1","gene_symbol":"LINC00563","gene_name":"long intergenic non-protein coding RNA 563 [Source:HGNC Symbol;Acc:HGNC:43707]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861554","summary":null,"start":46296445,"end":46297844,"strand":-1,"description":"long intergenic non-protein coding RNA 563 [Source:HGNC Symbol;Acc:HGNC:43707]"}, {"versioned_ensembl_gene_id":"ENSG00000166965.12","gene_symbol":"RCCD1","gene_name":"RCC1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30457]","synonyms":"MGC14386","biotype":"protein_coding","ncbi_id":"91433","summary":null,"start":90954870,"end":90963125,"strand":1,"description":"RCC1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30457]"}, {"versioned_ensembl_gene_id":"ENSG00000254654.1","gene_symbol":"AC068858.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44973902,"end":44978028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253697.1","gene_symbol":"AC103834.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9658295,"end":9658438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144810.15","gene_symbol":"COL8A1","gene_name":"collagen type VIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2215]","synonyms":"MGC9568,C3orf7","biotype":"protein_coding","ncbi_id":"1295","summary":"This gene encodes one of the two alpha chains of type VIII collagen. The gene product is a short chain collagen and a major component of the basement membrane of the corneal endothelium. The type VIII collagen fibril can be either a homo- or a heterotrimer. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Dec 2011]","start":99638475,"end":99799226,"strand":1,"description":"collagen type VIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2215]"}, {"versioned_ensembl_gene_id":"ENSG00000240246.1","gene_symbol":"AC108751.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149433044,"end":149433274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215493.3","gene_symbol":"AC007731.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20450122,"end":20451824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188536.12","gene_symbol":"HBA2","gene_name":"hemoglobin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4824]","synonyms":"HBA-T2","biotype":"protein_coding","ncbi_id":"3040","summary":"The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq, Jul 2008]","start":172847,"end":173710,"strand":1,"description":"hemoglobin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:4824]"}, {"versioned_ensembl_gene_id":"ENSG00000224382.1","gene_symbol":"LINC00703","gene_name":"long intergenic non-protein coding RNA 703 [Source:HGNC Symbol;Acc:HGNC:44677]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507059","summary":null,"start":4384246,"end":4410612,"strand":1,"description":"long intergenic non-protein coding RNA 703 [Source:HGNC Symbol;Acc:HGNC:44677]"}, {"versioned_ensembl_gene_id":"ENSG00000132321.16","gene_symbol":"IQCA1","gene_name":"IQ motif containing with AAA domain 1 [Source:HGNC Symbol;Acc:HGNC:26195]","synonyms":"IQCA,FLJ22527,DRC11","biotype":"protein_coding","ncbi_id":"79781","summary":"The protein encoded by this gene is a member of the ATPases Associated with diverse cellular Activities (AAA) superfamily. Members of this superfamily, found in all organisms, participate in a large number of cellular processes and contain the ATPase module consisting of an alpha-beta-alpha core domain and the Walker A and B motifs of the P-loop NTPases. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":236324147,"end":236507542,"strand":-1,"description":"IQ motif containing with AAA domain 1 [Source:HGNC Symbol;Acc:HGNC:26195]"}, {"versioned_ensembl_gene_id":"ENSG00000225609.1","gene_symbol":"CDY20P","gene_name":"chromodomain Y-linked 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:23864]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386742","summary":null,"start":25618644,"end":25620253,"strand":1,"description":"chromodomain Y-linked 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:23864]"}, {"versioned_ensembl_gene_id":"ENSG00000250307.2","gene_symbol":"TUBB8P3","gene_name":"tubulin beta 8 class VIII pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42338]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"132719","summary":null,"start":112077598,"end":112078400,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42338]"}, {"versioned_ensembl_gene_id":"ENSG00000278728.2","gene_symbol":"CNTNAP2","gene_name":"contactin associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13830]","synonyms":"NRXN4,KIAA0868,Caspr2","biotype":"protein_coding","ncbi_id":"26047","summary":"This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and is also involved in localization of potassium channels within differentiating axons. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by forkhead box protein P2, a transcription factor related to speech and language development. This gene has been implicated in multiple neurodevelopmental disorders, including Gilles de la Tourette syndrome, schizophrenia, epilepsy, autism, ADHD and intellectual disability. [provided by RefSeq, Jul 2017]","start":148217288,"end":148419466,"strand":1,"description":"contactin associated protein like 2 [Source:HGNC Symbol;Acc:HGNC:13830]"}, {"versioned_ensembl_gene_id":"ENSG00000134545.13","gene_symbol":"KLRC1","gene_name":"killer cell lectin like receptor C1 [Source:HGNC Symbol;Acc:HGNC:6374]","synonyms":"NKG2-B,NKG2-A,NKG2,CD159a","biotype":"protein_coding","ncbi_id":"3821","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. The protein encoded by this gene belongs to the killer cell lectin-like receptor family, also called NKG2 family, which is a group of transmembrane proteins preferentially expressed in NK cells. This family of proteins is characterized by the type II membrane orientation and the presence of a C-type lectin domain. This protein forms a complex with another family member, KLRD1/CD94, and has been implicated in the recognition of the MHC class I HLA-E molecules in NK cells. The genes of NKG2 family members form a killer cell lectin-like receptor gene cluster on chromosome 12. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jan 2015]","start":10442264,"end":10454685,"strand":-1,"description":"killer cell lectin like receptor C1 [Source:HGNC Symbol;Acc:HGNC:6374]"}, {"versioned_ensembl_gene_id":"ENSG00000249819.1","gene_symbol":"AC112240.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":157204462,"end":157204855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272729.1","gene_symbol":"AC009336.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176164164,"end":176165716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278415.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54545136,"end":54562282,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000132938.19","gene_symbol":"MTUS2","gene_name":"microtubule associated scaffold protein 2 [Source:HGNC Symbol;Acc:HGNC:20595]","synonyms":"CAZIP,TIP150,KIAA0774,ICIS","biotype":"protein_coding","ncbi_id":"23281","summary":null,"start":28820348,"end":29505947,"strand":1,"description":"microtubule associated scaffold protein 2 [Source:HGNC Symbol;Acc:HGNC:20595]"}, {"versioned_ensembl_gene_id":"ENSG00000179141.9","gene_symbol":"MTUS2-AS1","gene_name":"MTUS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40924]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874107","summary":null,"start":29476515,"end":29490105,"strand":-1,"description":"MTUS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40924]"}, {"versioned_ensembl_gene_id":"ENSG00000239304.1","gene_symbol":"DNM1P48","gene_name":"dynamin 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:38801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418739","summary":null,"start":25486640,"end":25487322,"strand":1,"description":"dynamin 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:38801]"}, {"versioned_ensembl_gene_id":"ENSG00000116819.6","gene_symbol":"TFAP2E","gene_name":"transcription factor AP-2 epsilon [Source:HGNC Symbol;Acc:HGNC:30774]","synonyms":"AP2E","biotype":"protein_coding","ncbi_id":"339488","summary":null,"start":35573370,"end":35595328,"strand":1,"description":"transcription factor AP-2 epsilon [Source:HGNC Symbol;Acc:HGNC:30774]"}, {"versioned_ensembl_gene_id":"ENSG00000228203.6","gene_symbol":"RNF144A-AS1","gene_name":"RNF144A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30963]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"386597","summary":null,"start":6912277,"end":6918709,"strand":-1,"description":"RNF144A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30963]"}, {"versioned_ensembl_gene_id":"ENSG00000125991.19","gene_symbol":"ERGIC3","gene_name":"ERGIC and golgi 3 [Source:HGNC Symbol;Acc:HGNC:15927]","synonyms":"PRO0989,NY-BR-84,Erv46,CGI-54,C20orf47,SDBCAG84","biotype":"protein_coding","ncbi_id":"51614","summary":null,"start":35542021,"end":35557634,"strand":1,"description":"ERGIC and golgi 3 [Source:HGNC Symbol;Acc:HGNC:15927]"}, {"versioned_ensembl_gene_id":"ENSG00000224497.1","gene_symbol":"RPL36P4","gene_name":"ribosomal protein L36 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16569]","synonyms":"dJ477O4.3","biotype":"processed_pseudogene","ncbi_id":"140750","summary":null,"start":35544430,"end":35544747,"strand":-1,"description":"ribosomal protein L36 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16569]"}, {"versioned_ensembl_gene_id":"ENSG00000231029.2","gene_symbol":"AL031733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167591392,"end":167591846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176923.5","gene_symbol":"OR7A15P","gene_name":"olfactory receptor family 7 subfamily A member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:8361]","synonyms":"OR7A4P,OR7A20P,OR7A16P,OR19-146,OR19-134,OR19-1","biotype":"unprocessed_pseudogene","ncbi_id":"26335","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14927052,"end":14928060,"strand":1,"description":"olfactory receptor family 7 subfamily A member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:8361]"}, {"versioned_ensembl_gene_id":"ENSG00000177370.4","gene_symbol":"TIMM22","gene_name":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]","synonyms":"TIM22,TEX4","biotype":"protein_coding","ncbi_id":"29928","summary":"Multipass transmembrane proteins are brought into mitochondria and inserted into the mitochondrial inner membrane by way of the TIM22 complex. This complex has six subunits and is a twin-pore translocase. The protein encoded by this gene is a subunit of TIM22 and represents the voltage-activated and signal-gated channel. [provided by RefSeq, Jul 2016]","start":997117,"end":1003671,"strand":1,"description":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]"}, {"versioned_ensembl_gene_id":"ENSG00000117632.22","gene_symbol":"STMN1","gene_name":"stathmin 1 [Source:HGNC Symbol;Acc:HGNC:6510]","synonyms":"OP18,LAP18,Lag,FLJ32206,C1orf215,SMN,PR22,PP19,PP17","biotype":"protein_coding","ncbi_id":"3925","summary":"This gene belongs to the stathmin family of genes. It encodes a ubiquitous cytosolic phosphoprotein proposed to function as an intracellular relay integrating regulatory signals of the cellular environment. The encoded protein is involved in the regulation of the microtubule filament system by destabilizing microtubules. It prevents assembly and promotes disassembly of microtubules. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":25884181,"end":25906991,"strand":-1,"description":"stathmin 1 [Source:HGNC Symbol;Acc:HGNC:6510]"}, {"versioned_ensembl_gene_id":"ENSG00000269787.2","gene_symbol":"OR7A3P","gene_name":"olfactory receptor family 7 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8366]","synonyms":"OR7A14P,OR7A14,OR7A13P,OR7A12P,OR19-12,OR14-59,OR14-11,OR11-7b","biotype":"unprocessed_pseudogene","ncbi_id":"26668","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14903232,"end":14904138,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:8366]"}, {"versioned_ensembl_gene_id":"ENSG00000255122.1","gene_symbol":"AC068587.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12580287,"end":12581063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249395.2","gene_symbol":"CASC9","gene_name":"cancer susceptibility 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48906]","synonyms":"LINC00981,ESCCAL-1","biotype":"lincRNA","ncbi_id":"101805492","summary":null,"start":75223404,"end":75324741,"strand":-1,"description":"cancer susceptibility 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48906]"}, {"versioned_ensembl_gene_id":"ENSG00000284613.1","gene_symbol":"AC068587.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12665278,"end":12665495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111845.4","gene_symbol":"PAK1IP1","gene_name":"PAK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20882]","synonyms":"MAK11,hPIP1,FLJ20624,bA421M1.5,WDR84,PIP1","biotype":"protein_coding","ncbi_id":"55003","summary":null,"start":10694695,"end":10709782,"strand":1,"description":"PAK1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20882]"}, {"versioned_ensembl_gene_id":"ENSG00000253229.1","gene_symbol":"HIGD1AP6","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43001]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874436","summary":null,"start":75302296,"end":75302574,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43001]"}, {"versioned_ensembl_gene_id":"ENSG00000242607.1","gene_symbol":"AC068587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12570350,"end":12571130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095585.16","gene_symbol":"BLNK","gene_name":"B-cell linker [Source:HGNC Symbol;Acc:HGNC:14211]","synonyms":"SLP65,SLP-65,Ly57,BLNK-s,bca,BASH","biotype":"protein_coding","ncbi_id":"29760","summary":"This gene encodes a cytoplasmic linker or adaptor protein that plays a critical role in B cell development. This protein bridges B cell receptor-associated kinase activation with downstream signaling pathways, thereby affecting various biological functions. The phosphorylation of five tyrosine residues is necessary for this protein to nucleate distinct signaling effectors following B cell receptor activation. Mutations in this gene cause hypoglobulinemia and absent B cells, a disease in which the pro- to pre-B-cell transition is developmentally blocked. Deficiency in this protein has also been shown in some cases of pre-B acute lymphoblastic leukemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]","start":96191702,"end":96271587,"strand":-1,"description":"B-cell linker [Source:HGNC Symbol;Acc:HGNC:14211]"}, {"versioned_ensembl_gene_id":"ENSG00000133316.15","gene_symbol":"WDR74","gene_name":"WD repeat domain 74 [Source:HGNC Symbol;Acc:HGNC:25529]","synonyms":"FLJ10439","biotype":"protein_coding","ncbi_id":"54663","summary":null,"start":62832342,"end":62841809,"strand":-1,"description":"WD repeat domain 74 [Source:HGNC Symbol;Acc:HGNC:25529]"}, {"versioned_ensembl_gene_id":"ENSG00000235315.2","gene_symbol":"RPL23AP69","gene_name":"ribosomal protein L23a pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:36625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271623","summary":null,"start":25206049,"end":25206506,"strand":1,"description":"ribosomal protein L23a pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:36625]"}, {"versioned_ensembl_gene_id":"ENSG00000236528.1","gene_symbol":"AL033528.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25859613,"end":25863420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283268.1","gene_symbol":"AP001160.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":62832319,"end":62832803,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218281.1","gene_symbol":"HIST1H2APS3","gene_name":"histone cluster 1 H2A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18805]","synonyms":"H2AFUP,dJ34B20.8","biotype":"unprocessed_pseudogene","ncbi_id":"387323","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This histone pseudogene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Oct 2015]","start":26233122,"end":26233255,"strand":1,"description":"histone cluster 1 H2A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:18805]"}, {"versioned_ensembl_gene_id":"ENSG00000243902.6","gene_symbol":"ELFN2","gene_name":"extracellular leucine rich repeat and fibronectin type III domain containing 2 [Source:NCBI gene;Acc:114794]","synonyms":"dJ63G5.3,PPP1R29,PPP1R29,LRRC62,LRRC62,KIAA1904","biotype":"sense_overlapping","ncbi_id":"114794","summary":null,"start":37339583,"end":37427445,"strand":-1,"description":"extracellular leucine rich repeat and fibronectin type III domain containing 2 [Source:NCBI gene;Acc:114794]"}, {"versioned_ensembl_gene_id":"ENSG00000183831.6","gene_symbol":"ANKRD45","gene_name":"ankyrin repeat domain 45 [Source:HGNC Symbol;Acc:HGNC:24786]","synonyms":"FLJ45235,CT117","biotype":"protein_coding","ncbi_id":"339416","summary":null,"start":173609561,"end":173669862,"strand":-1,"description":"ankyrin repeat domain 45 [Source:HGNC Symbol;Acc:HGNC:24786]"}, {"versioned_ensembl_gene_id":"ENSG00000239408.1","gene_symbol":"AC108751.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149464839,"end":149465201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282502.1","gene_symbol":"FKBP1AP4","gene_name":"FK506 binding protein 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3717]","synonyms":"FKBP1P4","biotype":"processed_pseudogene","ncbi_id":"2285","summary":null,"start":149463779,"end":149464114,"strand":-1,"description":"FK506 binding protein 1A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3717]"}, {"versioned_ensembl_gene_id":"ENSG00000143224.17","gene_symbol":"PPOX","gene_name":"protoporphyrinogen oxidase [Source:HGNC Symbol;Acc:HGNC:9280]","synonyms":"VP,PPO","biotype":"protein_coding","ncbi_id":"5498","summary":"This gene encodes the penultimate enzyme of heme biosynthesis, which catalyzes the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. Mutations in this gene cause variegate porphyria, an autosomal dominant disorder of heme metabolism resulting from a deficiency in protoporphyrinogen oxidase, an enzyme located on the inner mitochondrial membrane. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":161166410,"end":161178013,"strand":1,"description":"protoporphyrinogen oxidase [Source:HGNC Symbol;Acc:HGNC:9280]"}, {"versioned_ensembl_gene_id":"ENSG00000166800.9","gene_symbol":"LDHAL6A","gene_name":"lactate dehydrogenase A like 6A [Source:HGNC Symbol;Acc:HGNC:28335]","synonyms":"MGC23940,LDH6A","biotype":"protein_coding","ncbi_id":"160287","summary":null,"start":18455824,"end":18479600,"strand":1,"description":"lactate dehydrogenase A like 6A [Source:HGNC Symbol;Acc:HGNC:28335]"}, {"versioned_ensembl_gene_id":"ENSG00000165246.13","gene_symbol":"NLGN4Y","gene_name":"neuroligin 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:15529]","synonyms":"KIAA0951","biotype":"protein_coding","ncbi_id":"22829","summary":"This gene encodes a type I membrane protein that belongs to the family of neuroligins, which are cell adhesion molecules present at the postsynaptic side of the synapse, and may be essential for the formation of functional synapses. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Mar 2011]","start":14522638,"end":14845650,"strand":1,"description":"neuroligin 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:15529]"}, {"versioned_ensembl_gene_id":"ENSG00000256464.1","gene_symbol":"YWHABP2","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50295]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422666","summary":null,"start":18490243,"end":18490955,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50295]"}, {"versioned_ensembl_gene_id":"ENSG00000228787.1","gene_symbol":"NLGN4Y-AS1","gene_name":"NLGN4Y antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38793]","synonyms":"NLGN4Y-AS,NLGN4YAS","biotype":"antisense_RNA","ncbi_id":"100874056","summary":null,"start":14793642,"end":14804033,"strand":-1,"description":"NLGN4Y antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:38793]"}, {"versioned_ensembl_gene_id":"ENSG00000256588.1","gene_symbol":"AC027544.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18507608,"end":18508820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256361.1","gene_symbol":"AC027544.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18511043,"end":18511475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177553.6","gene_symbol":"AL953897.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11777077,"end":11779619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163599.14","gene_symbol":"CTLA4","gene_name":"cytotoxic T-lymphocyte associated protein 4 [Source:HGNC Symbol;Acc:HGNC:2505]","synonyms":"IDDM12,GSE,CELIAC3,CD152,CD","biotype":"protein_coding","ncbi_id":"1493","summary":"This gene is a member of the immunoglobulin superfamily and encodes a protein which transmits an inhibitory signal to T cells. The protein contains a V domain, a transmembrane domain, and a cytoplasmic tail. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. The membrane-bound isoform functions as a homodimer interconnected by a disulfide bond, while the soluble isoform functions as a monomer. Mutations in this gene have been associated with insulin-dependent diabetes mellitus, Graves disease, Hashimoto thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated orbitopathy, and other autoimmune diseases. [provided by RefSeq, Jul 2008]","start":203867786,"end":203873960,"strand":1,"description":"cytotoxic T-lymphocyte associated protein 4 [Source:HGNC Symbol;Acc:HGNC:2505]"}, {"versioned_ensembl_gene_id":"ENSG00000274684.4","gene_symbol":"NMRAL1","gene_name":"NmrA like redox sensor 1 [Source:HGNC Symbol;Acc:HGNC:24987]","synonyms":"SDR48A1,HSCARG,FLJ25918","biotype":"protein_coding","ncbi_id":"57407","summary":"This gene encodes an NADPH sensor protein that preferentially binds to NADPH. The encoded protein also negatively regulates the activity of NF-kappaB in a ubiquitylation-dependent manner. It plays a key role in cellular antiviral response by negatively regulating the interferon response factor 3-mediated expression of interferon beta. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":4463639,"end":4497722,"strand":-1,"description":"NmrA like redox sensor 1 [Source:HGNC Symbol;Acc:HGNC:24987]"}, {"versioned_ensembl_gene_id":"ENSG00000000971.15","gene_symbol":"CFH","gene_name":"complement factor H [Source:HGNC Symbol;Acc:HGNC:4883]","synonyms":"FHL1,ARMS1,ARMD4,HUS,HF2,HF1,HF","biotype":"protein_coding","ncbi_id":"3075","summary":"This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus repeat (SCR) domains. This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Oct 2011]","start":196651878,"end":196747504,"strand":1,"description":"complement factor H [Source:HGNC Symbol;Acc:HGNC:4883]"}, {"versioned_ensembl_gene_id":"ENSG00000235650.6","gene_symbol":"RPS18","gene_name":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]","synonyms":"S18,HKE3,KE3,D6S218E,KE-3","biotype":"protein_coding","ncbi_id":"6222","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S13P family of ribosomal proteins. It is located in the cytoplasm. The gene product of the E. coli ortholog (ribosomal protein S13) is involved in the binding of fMet-tRNA, and thus, in the initiation of translation. This gene is an ortholog of mouse Ke3. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":33193610,"end":33198110,"strand":1,"description":"ribosomal protein S18 [Source:HGNC Symbol;Acc:HGNC:10401]"}, {"versioned_ensembl_gene_id":"ENSG00000116745.6","gene_symbol":"RPE65","gene_name":"RPE65, retinoid isomerohydrolase [Source:HGNC Symbol;Acc:HGNC:10294]","synonyms":"RP20,rd12,LCA2,BCO3","biotype":"protein_coding","ncbi_id":"6121","summary":"The protein encoded by this gene is a component of the vitamin A visual cycle of the retina which supplies the 11-cis retinal chromophore of the photoreceptors opsin visual pigments. It is a member of the carotenoid cleavage oxygenase superfamily. All members of this superfamily are non-heme iron oxygenases with a seven-bladed propeller fold and oxidatively cleave carotenoid carbon:carbon double bonds. However, the protein encoded by this gene has acquired a divergent function that involves the concerted O-alkyl ester cleavage of its all-trans retinyl ester substrate and all-trans to 11-cis double bond isomerization of the retinyl moiety. As such, it performs the essential enzymatic isomerization step in the synthesis of 11-cis retinal. Mutations in this gene are associated with early-onset severe blinding disorders such as Leber congenital. [provided by RefSeq, Oct 2017]","start":68428822,"end":68449959,"strand":-1,"description":"RPE65, retinoid isomerohydrolase [Source:HGNC Symbol;Acc:HGNC:10294]"}, {"versioned_ensembl_gene_id":"ENSG00000257835.1","gene_symbol":"AC073591.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77379820,"end":77390864,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233321.1","gene_symbol":"AL357833.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3486894,"end":3502838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227338.1","gene_symbol":"AL139280.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3266003,"end":3267015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230291.5","gene_symbol":"AC078817.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80102899,"end":80103333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155875.13","gene_symbol":"SAXO1","gene_name":"stabilizer of axonemal microtubules 1 [Source:HGNC Symbol;Acc:HGNC:28566]","synonyms":"MGC35182,FAM154A,C9orf138","biotype":"protein_coding","ncbi_id":"158297","summary":null,"start":18927658,"end":19049354,"strand":-1,"description":"stabilizer of axonemal microtubules 1 [Source:HGNC Symbol;Acc:HGNC:28566]"}, {"versioned_ensembl_gene_id":"ENSG00000270980.1","gene_symbol":"AC060764.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54191582,"end":54192035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282935.1","gene_symbol":"ABBA01031661.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29410348,"end":29411600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236909.1","gene_symbol":"AL662791.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071824,"end":29072599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232271.1","gene_symbol":"AL096799.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7069614,"end":7146656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144655.14","gene_symbol":"CSRNP1","gene_name":"cysteine and serine rich nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:14300]","synonyms":"FAM130B,DKFZp566F164,AXUD1,URAX1,TAIP-3","biotype":"protein_coding","ncbi_id":"64651","summary":"This gene encodes a protein that localizes to the nucleus and expression of this gene is induced in response to elevated levels of axin. The Wnt signalling pathway, which is negatively regulated by axin, is important in axis formation in early development and impaired regulation of this signalling pathway is often involved in tumors. A decreased level of expression of this gene in tumors compared to the level of expression in their corresponding normal tissues suggests that this gene product has a tumor suppressor function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":39141855,"end":39154562,"strand":-1,"description":"cysteine and serine rich nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:14300]"}, {"versioned_ensembl_gene_id":"ENSG00000279074.1","gene_symbol":"AC007998.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35483431,"end":35483667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155330.9","gene_symbol":"C16orf87","gene_name":"chromosome 16 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:33754]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388272","summary":null,"start":46796607,"end":46831411,"strand":-1,"description":"chromosome 16 open reading frame 87 [Source:HGNC Symbol;Acc:HGNC:33754]"}, {"versioned_ensembl_gene_id":"ENSG00000135249.7","gene_symbol":"RINT1","gene_name":"RAD50 interactor 1 [Source:HGNC Symbol;Acc:HGNC:21876]","synonyms":"RINT-1,FLJ11785","biotype":"protein_coding","ncbi_id":"60561","summary":"This gene encodes a protein first identified for its ability to interact with the RAD50 double strand break repair protein, with the resulting interaction implicated in the regulation of cell cycle progression and telomere length. The encoded protein may also play a role in trafficking of cellular cargo from the endosome to the trans-Golgi network. Mutations in this gene may be associated with breast cancer in human patients. [provided by RefSeq, Oct 2016]","start":105532085,"end":105567677,"strand":1,"description":"RAD50 interactor 1 [Source:HGNC Symbol;Acc:HGNC:21876]"}, {"versioned_ensembl_gene_id":"ENSG00000253944.1","gene_symbol":"AC027117.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17801345,"end":17861069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282280.1","gene_symbol":"AC087382.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66270636,"end":66273940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229086.4","gene_symbol":"LINC01548","gene_name":"long intergenic non-protein coding RNA 1548 [Source:HGNC Symbol;Acc:HGNC:1296]","synonyms":"C21orf54","biotype":"lincRNA","ncbi_id":"728409","summary":null,"start":33165470,"end":33170649,"strand":-1,"description":"long intergenic non-protein coding RNA 1548 [Source:HGNC Symbol;Acc:HGNC:1296]"}, {"versioned_ensembl_gene_id":"ENSG00000136697.12","gene_symbol":"IL1F10","gene_name":"interleukin 1 family member 10 (theta) [Source:HGNC Symbol;Acc:HGNC:15552]","synonyms":"MGC119833,MGC119832,MGC11983,IL1-theta,IL-1HY2,IL-1F10,FKSG75","biotype":"protein_coding","ncbi_id":"84639","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. This cytokine is thought to participate in a network of interleukin 1 family members to regulate adapted and innate immune responses. Two alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":113067970,"end":113075850,"strand":1,"description":"interleukin 1 family member 10 (theta) [Source:HGNC Symbol;Acc:HGNC:15552]"}, {"versioned_ensembl_gene_id":"ENSG00000227214.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"antisense_RNA","ncbi_id":"414761","summary":null,"start":28986203,"end":28987484,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000244349.1","gene_symbol":"AL662791.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28986800,"end":28988536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243877.1","gene_symbol":"HMGB1P38","gene_name":"high mobility group box 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39185]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873895","summary":null,"start":79957566,"end":79958142,"strand":-1,"description":"high mobility group box 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:39185]"}, {"versioned_ensembl_gene_id":"ENSG00000225416.1","gene_symbol":"AC104843.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152602213,"end":152602892,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231139.1","gene_symbol":"AC104843.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152590641,"end":152590941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257964.1","gene_symbol":"AC020612.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49576840,"end":49577505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282770.1","gene_symbol":"DLG5-AS1","gene_name":"DLG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45109]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100128292","summary":null,"start":77927372,"end":77929824,"strand":1,"description":"DLG5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45109]"}, {"versioned_ensembl_gene_id":"ENSG00000268575.1","gene_symbol":"AL031282.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1702736,"end":1737688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232027.2","gene_symbol":"AL671986.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51372270,"end":51373224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115234.10","gene_symbol":"SNX17","gene_name":"sorting nexin 17 [Source:HGNC Symbol;Acc:HGNC:14979]","synonyms":"KIAA0064","biotype":"protein_coding","ncbi_id":"9784","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a B41 domain. This protein interacts with the cytoplasmic domain of P-selectin, and may function in the intracellular trafficking of P-selectin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012]","start":27370496,"end":27377533,"strand":1,"description":"sorting nexin 17 [Source:HGNC Symbol;Acc:HGNC:14979]"}, {"versioned_ensembl_gene_id":"ENSG00000176510.5","gene_symbol":"OR10AC1","gene_name":"olfactory receptor family 10 subfamily AC member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14758]","synonyms":"OR10AC1P","biotype":"polymorphic_pseudogene","ncbi_id":"392133","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":143509256,"end":143519469,"strand":-1,"description":"olfactory receptor family 10 subfamily AC member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14758]"}, {"versioned_ensembl_gene_id":"ENSG00000275495.3","gene_symbol":"AC114936.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":177875522,"end":177955274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280284.1","gene_symbol":"AC092608.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":156876435,"end":156876820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250280.2","gene_symbol":"AC026124.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":65281657,"end":65286728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216854.2","gene_symbol":"AL512422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56871191,"end":56871743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249036.1","gene_symbol":"AC092674.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77394491,"end":77494286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250006.2","gene_symbol":"AC008638.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77311397,"end":77312111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222007.6","gene_symbol":"AC064874.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":235773855,"end":235783387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163617.10","gene_symbol":"CCDC191","gene_name":"coiled-coil domain containing 191 [Source:HGNC Symbol;Acc:HGNC:29272]","synonyms":"KIAA1407","biotype":"protein_coding","ncbi_id":"57577","summary":null,"start":113964137,"end":114056613,"strand":-1,"description":"coiled-coil domain containing 191 [Source:HGNC Symbol;Acc:HGNC:29272]"}, {"versioned_ensembl_gene_id":"ENSG00000231896.1","gene_symbol":"AC019185.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":208469850,"end":208540413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284003.1","gene_symbol":"AC073869.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131373647,"end":131379675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227430.1","gene_symbol":"AC019185.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208466238,"end":208466626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169682.17","gene_symbol":"SPNS1","gene_name":"sphingolipid transporter 1 (putative) [Source:HGNC Symbol;Acc:HGNC:30621]","synonyms":"SPIN1,PP2030,nrs,LAT,HSpin1,SPINL","biotype":"protein_coding","ncbi_id":"83985","summary":null,"start":28974221,"end":28984548,"strand":1,"description":"sphingolipid transporter 1 (putative) [Source:HGNC Symbol;Acc:HGNC:30621]"}, {"versioned_ensembl_gene_id":"ENSG00000279907.1","gene_symbol":"AC018695.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85859521,"end":85862012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262505.2","gene_symbol":"ASIC5","gene_name":"acid sensing ion channel subunit family member 5 [Source:HGNC Symbol;Acc:HGNC:17537]","synonyms":"ACCN5,INAC,HINAC,ACCN5,INAC,HINAC","biotype":"protein_coding","ncbi_id":"51802","summary":"This gene belongs to the amiloride-sensitive Na+ channel and degenerin (NaC/DEG) family, members of which have been identified in many animal species ranging from the nematode to human. The amiloride-sensitive Na(+) channel encoded by this gene is primarily expressed in the small intestine, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":155836689,"end":155866273,"strand":-1,"description":"acid sensing ion channel subunit family member 5 [Source:HGNC Symbol;Acc:HGNC:17537]"}, {"versioned_ensembl_gene_id":"ENSG00000226789.1","gene_symbol":"AC110926.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127247258,"end":127250082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162687.16","gene_symbol":"KCNT2","gene_name":"potassium sodium-activated channel subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:18866]","synonyms":"SLICK,KCa4.2,SLO2.1","biotype":"protein_coding","ncbi_id":"343450","summary":null,"start":196225779,"end":196609225,"strand":-1,"description":"potassium sodium-activated channel subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:18866]"}, {"versioned_ensembl_gene_id":"ENSG00000269386.5","gene_symbol":"RAB11B-AS1","gene_name":"RAB11B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44178]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507567","summary":null,"start":8374373,"end":8390685,"strand":-1,"description":"RAB11B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44178]"}, {"versioned_ensembl_gene_id":"ENSG00000232606.1","gene_symbol":"LINC01412","gene_name":"long intergenic non-protein coding RNA 1412 [Source:HGNC Symbol;Acc:HGNC:50704]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928455","summary":null,"start":144566435,"end":144579434,"strand":1,"description":"long intergenic non-protein coding RNA 1412 [Source:HGNC Symbol;Acc:HGNC:50704]"}, {"versioned_ensembl_gene_id":"ENSG00000271771.1","gene_symbol":"AC139792.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34158121,"end":34158767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114503.10","gene_symbol":"NCBP2","gene_name":"nuclear cap binding protein subunit 2 [Source:HGNC Symbol;Acc:HGNC:7659]","synonyms":"NIP1,CBP20,Cbc2","biotype":"protein_coding","ncbi_id":"22916","summary":"The product of this gene is a component of the nuclear cap-binding protein complex (CBC), which binds to the monomethylated 5' cap of nascent pre-mRNA in the nucleoplasm. The encoded protein has an RNP domain commonly found in RNA binding proteins, and contains the cap-binding activity. The CBC promotes pre-mRNA splicing, 3'-end processing, RNA nuclear export, and nonsense-mediated mRNA decay. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":196935402,"end":196942597,"strand":-1,"description":"nuclear cap binding protein subunit 2 [Source:HGNC Symbol;Acc:HGNC:7659]"}, {"versioned_ensembl_gene_id":"ENSG00000128714.5","gene_symbol":"HOXD13","gene_name":"homeobox D13 [Source:HGNC Symbol;Acc:HGNC:5136]","synonyms":"SPD,HOX4I","biotype":"protein_coding","ncbi_id":"3239","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008]","start":176092891,"end":176095938,"strand":1,"description":"homeobox D13 [Source:HGNC Symbol;Acc:HGNC:5136]"}, {"versioned_ensembl_gene_id":"ENSG00000232106.9","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32300437,"end":32379326,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000226644.5","gene_symbol":"AL121899.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2207217,"end":2213151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204599.14","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30326479,"end":30343729,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000233908.1","gene_symbol":"AL359711.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109288440,"end":109288562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078747.14","gene_symbol":"ITCH","gene_name":"itchy E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:13890]","synonyms":"AIP4","biotype":"protein_coding","ncbi_id":"83737","summary":"This gene encodes a member of the Nedd4 family of HECT domain E3 ubiquitin ligases. HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates, thus targeting specific proteins for lysosomal degradation. The encoded protein plays a role in multiple cellular processes including erythroid and lymphoid cell differentiation and the regulation of immune responses. Mutations in this gene are a cause of syndromic multisystem autoimmune disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":34363235,"end":34511393,"strand":1,"description":"itchy E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:13890]"}, {"versioned_ensembl_gene_id":"ENSG00000280972.1","gene_symbol":"AP000432.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17659276,"end":17660384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274009.1","gene_symbol":"AC245128.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182591.5","gene_symbol":"KRTAP11-1","gene_name":"keratin associated protein 11-1 [Source:HGNC Symbol;Acc:HGNC:18922]","synonyms":"KAP11.1","biotype":"protein_coding","ncbi_id":"337880","summary":null,"start":30880644,"end":30881555,"strand":-1,"description":"keratin associated protein 11-1 [Source:HGNC Symbol;Acc:HGNC:18922]"}, {"versioned_ensembl_gene_id":"ENSG00000241912.1","gene_symbol":"AC078788.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153376831,"end":153377562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269926.1","gene_symbol":"DDIT4-AS1","gene_name":"DDIT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52379]","synonyms":"RP11-442H21.2","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72274915,"end":72275980,"strand":-1,"description":"DDIT4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52379]"}, {"versioned_ensembl_gene_id":"ENSG00000270099.1","gene_symbol":"AL365273.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":95860548,"end":95924844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276332.1","gene_symbol":"AC010338.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38197432,"end":38198148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276538.1","gene_symbol":"AC092666.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":150047609,"end":150047854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271253.1","gene_symbol":"AC011891.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12685637,"end":12686033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250654.7","gene_symbol":"AC023794.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54076838,"end":54081903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227850.1","gene_symbol":"SEPT2P1","gene_name":"septin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873333","summary":null,"start":105698039,"end":105698218,"strand":1,"description":"septin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:40017]"}, {"versioned_ensembl_gene_id":"ENSG00000007384.15","gene_symbol":"RHBDF1","gene_name":"rhomboid 5 homolog 1 [Source:HGNC Symbol;Acc:HGNC:20561]","synonyms":"iRhom1,FLJ2235,EGFR-RS,Dist1,C16orf8","biotype":"protein_coding","ncbi_id":"64285","summary":null,"start":58059,"end":76355,"strand":-1,"description":"rhomboid 5 homolog 1 [Source:HGNC Symbol;Acc:HGNC:20561]"}, {"versioned_ensembl_gene_id":"ENSG00000229201.1","gene_symbol":"AC092783.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90510910,"end":90533472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102904.14","gene_symbol":"TSNAXIP1","gene_name":"translin associated factor X interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18586]","synonyms":"TXI1","biotype":"protein_coding","ncbi_id":"55815","summary":null,"start":67806765,"end":67832148,"strand":1,"description":"translin associated factor X interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18586]"}, {"versioned_ensembl_gene_id":"ENSG00000185013.16","gene_symbol":"NT5C1B","gene_name":"5'-nucleotidase, cytosolic IB [Source:HGNC Symbol;Acc:HGNC:17818]","synonyms":"CN-IB,AIRP","biotype":"protein_coding","ncbi_id":"93034","summary":"Cytosolic 5-prime nucleotidases, such as NT5C1B, catalyze production of adenosine, which regulates diverse physiologic processes (Sala-Newby and Newby, 2001 [PubMed 11690631]).[supplied by OMIM, Mar 2008]","start":18562872,"end":18589572,"strand":-1,"description":"5'-nucleotidase, cytosolic IB [Source:HGNC Symbol;Acc:HGNC:17818]"}, {"versioned_ensembl_gene_id":"ENSG00000072954.6","gene_symbol":"TMEM38A","gene_name":"transmembrane protein 38A [Source:HGNC Symbol;Acc:HGNC:28462]","synonyms":"TRIC-A,MGC3169","biotype":"protein_coding","ncbi_id":"79041","summary":null,"start":16661127,"end":16690029,"strand":1,"description":"transmembrane protein 38A [Source:HGNC Symbol;Acc:HGNC:28462]"}, {"versioned_ensembl_gene_id":"ENSG00000010278.12","gene_symbol":"CD9","gene_name":"CD9 molecule [Source:HGNC Symbol;Acc:HGNC:1709]","synonyms":"BA2,TSPAN29,P24,MRP-1,MIC3","biotype":"protein_coding","ncbi_id":"928","summary":"This gene encodes a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Tetraspanins are cell surface glycoproteins with four transmembrane domains that form multimeric complexes with other cell surface proteins. The encoded protein functions in many cellular processes including differentiation, adhesion, and signal transduction, and expression of this gene plays a critical role in the suppression of cancer cell motility and metastasis. [provided by RefSeq, Jan 2011]","start":6199715,"end":6238271,"strand":1,"description":"CD9 molecule [Source:HGNC Symbol;Acc:HGNC:1709]"}, {"versioned_ensembl_gene_id":"ENSG00000235165.2","gene_symbol":"CDK5P1","gene_name":"cyclin dependent kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21261]","synonyms":"CDK5PS","biotype":"processed_pseudogene","ncbi_id":"392265","summary":null,"start":122769274,"end":122770150,"strand":1,"description":"cyclin dependent kinase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21261]"}, {"versioned_ensembl_gene_id":"ENSG00000231811.2","gene_symbol":"AL159166.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4345743,"end":4347037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273455.1","gene_symbol":"AC072039.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136087475,"end":136087913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244267.1","gene_symbol":"RPL34P22","gene_name":"ribosomal protein L34 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271498","summary":null,"start":44629357,"end":44629674,"strand":1,"description":"ribosomal protein L34 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:36454]"}, {"versioned_ensembl_gene_id":"ENSG00000214460.3","gene_symbol":"TPT1P6","gene_name":"tumor protein, translationally-controlled 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49297]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643870","summary":null,"start":85427453,"end":85427966,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49297]"}, {"versioned_ensembl_gene_id":"ENSG00000251548.1","gene_symbol":"AC106760.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10664495,"end":10665113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279979.1","gene_symbol":"AC012629.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10675317,"end":10675575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233640.2","gene_symbol":"KRTAP13-5P","gene_name":"keratin associated protein 13-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18929]","synonyms":"KRTAP13P1,KAP13A","biotype":"unprocessed_pseudogene","ncbi_id":"337964","summary":null,"start":30436466,"end":30436964,"strand":-1,"description":"keratin associated protein 13-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18929]"}, {"versioned_ensembl_gene_id":"ENSG00000277561.4","gene_symbol":"GOLGA8IP","gene_name":"golgin A8 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:26660]","synonyms":"GOLGA9P,GOLGA8I,FLJ35785","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"283796","summary":null,"start":22607540,"end":22617854,"strand":-1,"description":"golgin A8 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:26660]"}, {"versioned_ensembl_gene_id":"ENSG00000240432.3","gene_symbol":"KRTAP13-3","gene_name":"keratin associated protein 13-3 [Source:HGNC Symbol;Acc:HGNC:18925]","synonyms":"KAP13.3","biotype":"protein_coding","ncbi_id":"337960","summary":null,"start":30425265,"end":30425968,"strand":-1,"description":"keratin associated protein 13-3 [Source:HGNC Symbol;Acc:HGNC:18925]"}, {"versioned_ensembl_gene_id":"ENSG00000284744.1","gene_symbol":"AL591163.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6767954,"end":6770038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165171.10","gene_symbol":"METTL27","gene_name":"methyltransferase like 27 [Source:HGNC Symbol;Acc:HGNC:19068]","synonyms":"WBSCR27","biotype":"protein_coding","ncbi_id":"155368","summary":"This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]","start":73834590,"end":73842535,"strand":-1,"description":"methyltransferase like 27 [Source:HGNC Symbol;Acc:HGNC:19068]"}, {"versioned_ensembl_gene_id":"ENSG00000228221.5","gene_symbol":"LINC00578","gene_name":"long intergenic non-protein coding RNA 578 [Source:HGNC Symbol;Acc:HGNC:43807]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505566","summary":null,"start":177441921,"end":177752305,"strand":1,"description":"long intergenic non-protein coding RNA 578 [Source:HGNC Symbol;Acc:HGNC:43807]"}, {"versioned_ensembl_gene_id":"ENSG00000218549.1","gene_symbol":"OR4K12P","gene_name":"olfactory receptor family 4 subfamily K member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15403]","synonyms":"OR21-2","biotype":"processed_pseudogene","ncbi_id":"81078","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":13581044,"end":13582004,"strand":-1,"description":"olfactory receptor family 4 subfamily K member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:15403]"}, {"versioned_ensembl_gene_id":"ENSG00000183304.10","gene_symbol":"FAM9A","gene_name":"family with sequence similarity 9 member A [Source:HGNC Symbol;Acc:HGNC:18403]","synonyms":"TEX39A","biotype":"protein_coding","ncbi_id":"171482","summary":"This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be a nuclear protein that is localized to the nucleolus, and has some similarity to a synaptonemal complex protein. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2011]","start":8790795,"end":8801383,"strand":-1,"description":"family with sequence similarity 9 member A [Source:HGNC Symbol;Acc:HGNC:18403]"}, {"versioned_ensembl_gene_id":"ENSG00000228953.1","gene_symbol":"AC006026.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23655682,"end":23655861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239872.1","gene_symbol":"RPL35AP19","gene_name":"ribosomal protein L35a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271322","summary":null,"start":121380137,"end":121380465,"strand":-1,"description":"ribosomal protein L35a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36631]"}, {"versioned_ensembl_gene_id":"ENSG00000187481.2","gene_symbol":"HSD3BP1","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5219]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391076","summary":null,"start":119467221,"end":119473803,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5219]"}, {"versioned_ensembl_gene_id":"ENSG00000261310.1","gene_symbol":"AC009081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60486819,"end":60523250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232780.2","gene_symbol":"GAPDHP74","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:50647]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"391073","summary":null,"start":119434166,"end":119435080,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:50647]"}, {"versioned_ensembl_gene_id":"ENSG00000254765.1","gene_symbol":"AC011092.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9958744,"end":9959790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180263.13","gene_symbol":"FGD6","gene_name":"FYVE, RhoGEF and PH domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21740]","synonyms":"ZFYVE24,FLJ11183","biotype":"protein_coding","ncbi_id":"55785","summary":null,"start":95076749,"end":95217482,"strand":-1,"description":"FYVE, RhoGEF and PH domain containing 6 [Source:HGNC Symbol;Acc:HGNC:21740]"}, {"versioned_ensembl_gene_id":"ENSG00000139767.9","gene_symbol":"SRRM4","gene_name":"serine/arginine repetitive matrix 4 [Source:HGNC Symbol;Acc:HGNC:29389]","synonyms":"nSR100,KIAA1853","biotype":"protein_coding","ncbi_id":"84530","summary":"SRRM4 promotes alternative splicing and inclusion of neural-specific exons in target mRNAs (Calarco et al., 2009 [PubMed 19737518]).[supplied by OMIM, Oct 2009]","start":118981495,"end":119163051,"strand":1,"description":"serine/arginine repetitive matrix 4 [Source:HGNC Symbol;Acc:HGNC:29389]"}, {"versioned_ensembl_gene_id":"ENSG00000263310.5","gene_symbol":"SALL3","gene_name":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]","synonyms":"ZNF796","biotype":"protein_coding","ncbi_id":"27164","summary":"This gene encodes a sal-like C2H2-type zinc-finger protein, and belongs to a family of evolutionarily conserved genes found in species as diverse as Drosophila, C. elegans, and vertebrates. Mutations in some of these genes are associated with congenital disorders in human, suggesting their importance in embryonic development. This protein binds to DNA methyltransferase 3 alpha (DNMT3A), and reduces DNMT3A-mediated CpG island methylation. It is suggested that silencing of this gene, resulting in acceleration of DNA methylation, may have a role in oncogenesis. [provided by RefSeq, Oct 2011]","start":78980275,"end":79002678,"strand":1,"description":"spalt like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10527]"}, {"versioned_ensembl_gene_id":"ENSG00000254865.1","gene_symbol":"AC100763.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10149192,"end":10165109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239608.1","gene_symbol":"RUVBL1-AS1","gene_name":"RUVBL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40514]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874089","summary":null,"start":128075810,"end":128079056,"strand":1,"description":"RUVBL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40514]"}, {"versioned_ensembl_gene_id":"ENSG00000175792.11","gene_symbol":"RUVBL1","gene_name":"RuvB like AAA ATPase 1 [Source:HGNC Symbol;Acc:HGNC:10474]","synonyms":"TIP49,TIH1,RVB1,Pontin52,NMP238,INO80H,ECP54,TIP49a","biotype":"protein_coding","ncbi_id":"8607","summary":"This gene encodes a protein that has both DNA-dependent ATPase and DNA helicase activities and belongs to the ATPases associated with diverse cellular activities (AAA+) protein family. The encoded protein associates with several multisubunit transcriptional complexes and with protein complexes involved in both ATP-dependent remodeling and histone modification. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":128064778,"end":128153914,"strand":-1,"description":"RuvB like AAA ATPase 1 [Source:HGNC Symbol;Acc:HGNC:10474]"}, {"versioned_ensembl_gene_id":"ENSG00000099974.7","gene_symbol":"DDTL","gene_name":"D-dopachrome tautomerase like [Source:HGNC Symbol;Acc:HGNC:33446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100037417","summary":null,"start":23966901,"end":23972532,"strand":1,"description":"D-dopachrome tautomerase like [Source:HGNC Symbol;Acc:HGNC:33446]"}, {"versioned_ensembl_gene_id":"ENSG00000236893.1","gene_symbol":"ASS1P7","gene_name":"argininosuccinate synthetase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:770]","synonyms":"ASSP7","biotype":"processed_pseudogene","ncbi_id":"339845","summary":null,"start":177297161,"end":177298386,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:770]"}, {"versioned_ensembl_gene_id":"ENSG00000234729.9","gene_symbol":"AGER","gene_name":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]","synonyms":"SCARJ1,RAGE","biotype":"protein_coding","ncbi_id":"177","summary":"The advanced glycosylation end product (AGE) receptor encoded by this gene is a member of the immunoglobulin superfamily of cell surface receptors. It is a multiligand receptor, and besides AGE, interacts with other molecules implicated in homeostasis, development, and inflammation, and certain diseases, such as diabetes and Alzheimer's disease. Many alternatively spliced transcript variants encoding different isoforms, as well as non-protein-coding variants, have been described for this gene (PMID:18089847). [provided by RefSeq, May 2011]","start":32129439,"end":32132795,"strand":-1,"description":"advanced glycosylation end-product specific receptor [Source:HGNC Symbol;Acc:HGNC:320]"}, {"versioned_ensembl_gene_id":"ENSG00000203859.9","gene_symbol":"HSD3B2","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 [Source:HGNC Symbol;Acc:HGNC:5218]","synonyms":"SDR11E2","biotype":"protein_coding","ncbi_id":"3284","summary":"The protein encoded by this gene is a bifunctional enzyme that catalyzes the oxidative conversion of delta(5)-ene-3-beta-hydroxy steroid, and the oxidative conversion of ketosteroids. It plays a crucial role in the biosynthesis of all classes of hormonal steroids. This gene is predominantly expressed in the adrenals and the gonads. Mutations in this gene are associated with 3-beta-hydroxysteroid dehydrogenase, type II, deficiency. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2009]","start":119414931,"end":119423035,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 [Source:HGNC Symbol;Acc:HGNC:5218]"}, {"versioned_ensembl_gene_id":"ENSG00000280149.1","gene_symbol":"AC004877.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":149851572,"end":149852170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271027.1","gene_symbol":"AC006380.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31330711,"end":31330896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217442.3","gene_symbol":"SYCE3","gene_name":"synaptonemal complex central element protein 3 [Source:HGNC Symbol;Acc:HGNC:35245]","synonyms":"C22orf41","biotype":"protein_coding","ncbi_id":"644186","summary":null,"start":50551112,"end":50562905,"strand":-1,"description":"synaptonemal complex central element protein 3 [Source:HGNC Symbol;Acc:HGNC:35245]"}, {"versioned_ensembl_gene_id":"ENSG00000280431.1","gene_symbol":"AL160394.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34079411,"end":34080134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137413.15","gene_symbol":"TAF8","gene_name":"TATA-box binding protein associated factor 8 [Source:HGNC Symbol;Acc:HGNC:17300]","synonyms":"TBN,TAF(II)43,FLJ32821","biotype":"protein_coding","ncbi_id":"129685","summary":"This gene encodes one of several TATA-binding protein (TBP)-associated factors (TAFs), which are integral subunits of the general transcription factor complex TFIID. TFIID recognizes the core promoter of many genes and nucleates the assembly of a transcription preinitiation complex containing RNA polymerase II and other initiation factors. The protein encoded by this gene contains an H4-like histone fold domain, and interacts with several subunits of TFIID including TBP and the histone-fold protein TAF10. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":42050513,"end":42087461,"strand":1,"description":"TATA-box binding protein associated factor 8 [Source:HGNC Symbol;Acc:HGNC:17300]"}, {"versioned_ensembl_gene_id":"ENSG00000204614.8","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30136108,"end":30148735,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000233482.1","gene_symbol":"AC093579.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94145111,"end":94145619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149451.17","gene_symbol":"ADAM33","gene_name":"ADAM metallopeptidase domain 33 [Source:HGNC Symbol;Acc:HGNC:15478]","synonyms":"DKFZp434K0521,dJ964F7.1,C20orf153","biotype":"protein_coding","ncbi_id":"80332","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This protein is a type I transmembrane protein implicated in asthma and bronchial hyperresponsiveness. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013]","start":3667965,"end":3682246,"strand":-1,"description":"ADAM metallopeptidase domain 33 [Source:HGNC Symbol;Acc:HGNC:15478]"}, {"versioned_ensembl_gene_id":"ENSG00000274400.1","gene_symbol":"AC015967.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35144942,"end":35145417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188694.5","gene_symbol":"KRTAP24-1","gene_name":"keratin associated protein 24-1 [Source:HGNC Symbol;Acc:HGNC:33902]","synonyms":"KAP24.1","biotype":"protein_coding","ncbi_id":"643803","summary":null,"start":30281309,"end":30282958,"strand":-1,"description":"keratin associated protein 24-1 [Source:HGNC Symbol;Acc:HGNC:33902]"}, {"versioned_ensembl_gene_id":"ENSG00000231271.1","gene_symbol":"AP000350.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23949918,"end":23954042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233741.1","gene_symbol":"AC016691.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119993199,"end":119993611,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260626.1","gene_symbol":"AC136944.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33533816,"end":33534976,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231226.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104533120","summary":null,"start":30105240,"end":30114724,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000263322.1","gene_symbol":"AC110597.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67551243,"end":67554415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233395.1","gene_symbol":"LINC00841","gene_name":"long intergenic non-protein coding RNA 841 [Source:HGNC Symbol;Acc:HGNC:27430]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283033","summary":null,"start":43939003,"end":43944466,"strand":1,"description":"long intergenic non-protein coding RNA 841 [Source:HGNC Symbol;Acc:HGNC:27430]"}, {"versioned_ensembl_gene_id":"ENSG00000261144.1","gene_symbol":"AC092121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59166951,"end":59167152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179817.5","gene_symbol":"MRGPRX4","gene_name":"MAS related GPR family member X4 [Source:HGNC Symbol;Acc:HGNC:17617]","synonyms":"MRGX4","biotype":"protein_coding","ncbi_id":"117196","summary":null,"start":18172837,"end":18174280,"strand":1,"description":"MAS related GPR family member X4 [Source:HGNC Symbol;Acc:HGNC:17617]"}, {"versioned_ensembl_gene_id":"ENSG00000255138.1","gene_symbol":"GLTPP1","gene_name":"glycolipid transfer protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33991]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645312","summary":null,"start":18189000,"end":18189621,"strand":1,"description":"glycolipid transfer protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33991]"}, {"versioned_ensembl_gene_id":"ENSG00000206147.5","gene_symbol":"RPL23AP57","gene_name":"ribosomal protein L23a pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:36971]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648294","summary":null,"start":6639139,"end":6639604,"strand":1,"description":"ribosomal protein L23a pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:36971]"}, {"versioned_ensembl_gene_id":"ENSG00000227132.5","gene_symbol":"CR759772.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31089020,"end":31113948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248539.1","gene_symbol":"LINC02117","gene_name":"long intergenic non-protein coding RNA 2117 [Source:HGNC Symbol;Acc:HGNC:52972]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374728","summary":null,"start":37899363,"end":37920869,"strand":-1,"description":"long intergenic non-protein coding RNA 2117 [Source:HGNC Symbol;Acc:HGNC:52972]"}, {"versioned_ensembl_gene_id":"ENSG00000146674.14","gene_symbol":"IGFBP3","gene_name":"insulin like growth factor binding protein 3 [Source:HGNC Symbol;Acc:HGNC:5472]","synonyms":"IBP3,BP-53","biotype":"protein_coding","ncbi_id":"3486","summary":"This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP domain and a thyroglobulin type-I domain. The protein forms a ternary complex with insulin-like growth factor acid-labile subunit (IGFALS) and either insulin-like growth factor (IGF) I or II. In this form, it circulates in the plasma, prolonging the half-life of IGFs and altering their interaction with cell surface receptors. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":45912245,"end":45921874,"strand":-1,"description":"insulin like growth factor binding protein 3 [Source:HGNC Symbol;Acc:HGNC:5472]"}, {"versioned_ensembl_gene_id":"ENSG00000277466.1","gene_symbol":"AP006248.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17596312,"end":17596378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169740.13","gene_symbol":"ZNF32","gene_name":"zinc finger protein 32 [Source:HGNC Symbol;Acc:HGNC:13095]","synonyms":"KOX30","biotype":"protein_coding","ncbi_id":"7580","summary":null,"start":43643859,"end":43648856,"strand":-1,"description":"zinc finger protein 32 [Source:HGNC Symbol;Acc:HGNC:13095]"}, {"versioned_ensembl_gene_id":"ENSG00000238138.1","gene_symbol":"AC027124.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13460294,"end":13460398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184923.12","gene_symbol":"NUTM2A","gene_name":"NUT family member 2A [Source:HGNC Symbol;Acc:HGNC:23438]","synonyms":"FAM22A","biotype":"protein_coding","ncbi_id":"728118","summary":null,"start":87225448,"end":87236908,"strand":1,"description":"NUT family member 2A [Source:HGNC Symbol;Acc:HGNC:23438]"}, {"versioned_ensembl_gene_id":"ENSG00000198324.13","gene_symbol":"FAM109A","gene_name":"family with sequence similarity 109 member A [Source:HGNC Symbol;Acc:HGNC:26509]","synonyms":"IPIP27A,FLJ32356,SES1","biotype":"protein_coding","ncbi_id":"144717","summary":"This gene encodes a protein that localizes to the endosome and interacts with the enzyme, inositol polyphosphate 5-phosphatase OCRL-1. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":111360651,"end":111369121,"strand":-1,"description":"family with sequence similarity 109 member A [Source:HGNC Symbol;Acc:HGNC:26509]"}, {"versioned_ensembl_gene_id":"ENSG00000225778.5","gene_symbol":"PROSER2-AS1","gene_name":"PROSER2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27343]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"219731","summary":null,"start":11849608,"end":11894700,"strand":-1,"description":"PROSER2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27343]"}, {"versioned_ensembl_gene_id":"ENSG00000229596.3","gene_symbol":"MYL8P","gene_name":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]","synonyms":"BING3","biotype":"processed_pseudogene","ncbi_id":"442204","summary":null,"start":33338978,"end":33339495,"strand":1,"description":"myosin light chain 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:7589]"}, {"versioned_ensembl_gene_id":"ENSG00000267728.3","gene_symbol":"KRTAP9-9","gene_name":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]","synonyms":"KRTAP9-5,KAP9.9,KAP9.5,KRTAP9-5,KAP9.9,KAP9.5","biotype":"protein_coding","ncbi_id":"81870","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. Alternative haplotypes of this gene are represented in the GRCh38 reference genome assembly. [provided by RefSeq, Dec 2015]","start":41255319,"end":41256311,"strand":1,"description":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]"}, {"versioned_ensembl_gene_id":"ENSG00000106144.19","gene_symbol":"CASP2","gene_name":"caspase 2 [Source:HGNC Symbol;Acc:HGNC:1503]","synonyms":"PPP1R57,NEDD2,MGC2181,ICH1","biotype":"protein_coding","ncbi_id":"835","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Caspases mediate cellular apoptosis through the proteolytic cleavage of specific protein substrates. The encoded protein may function in stress-induced cell death pathways, cell cycle maintenance, and the suppression of tumorigenesis. Increased expression of this gene may play a role in neurodegenerative disorders including Alzheimer's disease, Huntington's disease and temporal lobe epilepsy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":143288215,"end":143307696,"strand":1,"description":"caspase 2 [Source:HGNC Symbol;Acc:HGNC:1503]"}, {"versioned_ensembl_gene_id":"ENSG00000127616.17","gene_symbol":"SMARCA4","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 [Source:HGNC Symbol;Acc:HGNC:11100]","synonyms":"SWI2,SNF2LB,SNF2L4,SNF2-BETA,SNF2,hSNF2b,FLJ39786,BRG1,BAF190","biotype":"protein_coding","ncbi_id":"6597","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins and is similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. In addition, this protein can bind BRCA1, as well as regulate the expression of the tumorigenic protein CD44. Mutations in this gene cause rhabdoid tumor predisposition syndrome type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":10961001,"end":11065395,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 [Source:HGNC Symbol;Acc:HGNC:11100]"}, {"versioned_ensembl_gene_id":"ENSG00000272146.5","gene_symbol":"ARF4-AS1","gene_name":"ARF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51593]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106144532","summary":null,"start":57597715,"end":57600927,"strand":1,"description":"ARF4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51593]"}, {"versioned_ensembl_gene_id":"ENSG00000273872.1","gene_symbol":"SLC25A15P4","gene_name":"solute carrier family 25 member 15 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39845]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422636","summary":null,"start":10612455,"end":10613379,"strand":-1,"description":"solute carrier family 25 member 15 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39845]"}, {"versioned_ensembl_gene_id":"ENSG00000275115.1","gene_symbol":"AC067904.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27010486,"end":27010746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270416.2","gene_symbol":"REXO1L4P","gene_name":"REXO1 like 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:32241]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653042","summary":null,"start":85802574,"end":85806435,"strand":-1,"description":"REXO1 like 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:32241]"}, {"versioned_ensembl_gene_id":"ENSG00000261298.1","gene_symbol":"AC122134.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234222838,"end":234224514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231417.2","gene_symbol":"IRX1P1","gene_name":"iroquois homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33315]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646390","summary":null,"start":24742677,"end":24746184,"strand":1,"description":"iroquois homeobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33315]"}, {"versioned_ensembl_gene_id":"ENSG00000143921.6","gene_symbol":"ABCG8","gene_name":"ATP binding cassette subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:13887]","synonyms":"GBD4","biotype":"protein_coding","ncbi_id":"64241","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions to exclude non-cholesterol sterol entry at the intestinal level, promote excretion of cholesterol and sterols into bile, and to facilitate transport of sterols back into the intestinal lumen. It is expressed in a tissue-specific manner in the liver, intestine, and gallbladder. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG5. Mutations in this gene may contribute to sterol accumulation and atherosclerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008]","start":43838964,"end":43878466,"strand":1,"description":"ATP binding cassette subfamily G member 8 [Source:HGNC Symbol;Acc:HGNC:13887]"}, {"versioned_ensembl_gene_id":"ENSG00000173113.6","gene_symbol":"TRMT112","gene_name":"tRNA methyltransferase subunit 11-2 [Source:HGNC Symbol;Acc:HGNC:26940]","synonyms":"hTrm112,HSPC170,HSPC152,TRMT11-2,TRM112","biotype":"protein_coding","ncbi_id":"51504","summary":null,"start":64316460,"end":64318084,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 [Source:HGNC Symbol;Acc:HGNC:26940]"}, {"versioned_ensembl_gene_id":"ENSG00000225658.1","gene_symbol":"TAF13P2","gene_name":"TATA-box binding protein associated factor 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38161]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462886","summary":null,"start":74351134,"end":74351419,"strand":1,"description":"TATA-box binding protein associated factor 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38161]"}, {"versioned_ensembl_gene_id":"ENSG00000234521.2","gene_symbol":"AC005041.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":74407797,"end":74413603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171492.14","gene_symbol":"LRRC8D","gene_name":"leucine rich repeat containing 8 family member D [Source:HGNC Symbol;Acc:HGNC:16992]","synonyms":"LRRC5,FLJ10470","biotype":"protein_coding","ncbi_id":"55144","summary":null,"start":89821014,"end":89936611,"strand":1,"description":"leucine rich repeat containing 8 family member D [Source:HGNC Symbol;Acc:HGNC:16992]"}, {"versioned_ensembl_gene_id":"ENSG00000120333.4","gene_symbol":"MRPS14","gene_name":"mitochondrial ribosomal protein S14 [Source:HGNC Symbol;Acc:HGNC:14049]","synonyms":"HSMRPS14","biotype":"protein_coding","ncbi_id":"63931","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S14P family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":175010789,"end":175023425,"strand":-1,"description":"mitochondrial ribosomal protein S14 [Source:HGNC Symbol;Acc:HGNC:14049]"}, {"versioned_ensembl_gene_id":"ENSG00000231714.1","gene_symbol":"AL513348.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194350943,"end":194352426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274193.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789815,"end":54800891,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000143217.8","gene_symbol":"NECTIN4","gene_name":"nectin cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:19688]","synonyms":"PVRL4,PRR4,nectin-4,LNIR","biotype":"protein_coding","ncbi_id":"81607","summary":"This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.[provided by RefSeq, Jan 2011]","start":161070995,"end":161089599,"strand":-1,"description":"nectin cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:19688]"}, {"versioned_ensembl_gene_id":"ENSG00000239883.8","gene_symbol":"PARGP1","gene_name":"poly(ADP-ribose) glycohydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45008]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728407","summary":null,"start":45854093,"end":45972154,"strand":-1,"description":"poly(ADP-ribose) glycohydrolase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45008]"}, {"versioned_ensembl_gene_id":"ENSG00000180389.6","gene_symbol":"ATP5EP2","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34026]","synonyms":null,"biotype":"protein_coding","ncbi_id":"432369","summary":null,"start":27945206,"end":27945590,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34026]"}, {"versioned_ensembl_gene_id":"ENSG00000268505.1","gene_symbol":"AC135012.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86192793,"end":86198913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260141.1","gene_symbol":"AC145350.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33043609,"end":33095431,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105278.10","gene_symbol":"ZFR2","gene_name":"zinc finger RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29189]","synonyms":"KIAA1086","biotype":"protein_coding","ncbi_id":"23217","summary":null,"start":3804024,"end":3869032,"strand":-1,"description":"zinc finger RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29189]"}, {"versioned_ensembl_gene_id":"ENSG00000240498.6","gene_symbol":"CDKN2B-AS1","gene_name":"CDKN2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34341]","synonyms":"RP11-145E5.4,PCAT12,p15AS,NCRNA00089,CDKN2BAS,CDKN2B-AS,ANRIL","biotype":"antisense_RNA","ncbi_id":"100048912","summary":"This gene is located within the CDKN2B-CDKN2A gene cluster at chromosome 9p21. The gene product is a functional RNA molecule that interacts with polycomb repressive complex-1 (PRC1) and -2 (PRC2), leading to epigenetic silencing of other genes in this cluster. This region is a significant genetic susceptibility locus for cardiovascular disease, and has also been linked to a number of other pathologies, including several cancers, intracranial aneurysm, type-2 diabetes, periodontitis, Alzheimer's disease, endometriosis, frailty in the elderly, and glaucoma. Multiple alternatively processed transcript variants have been detected, some of which may take the form of circular RNA molecules (PMID:21151960). [provided by RefSeq, May 2014]","start":21994778,"end":22121097,"strand":1,"description":"CDKN2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34341]"}, {"versioned_ensembl_gene_id":"ENSG00000263296.2","gene_symbol":"KRTAP3-2","gene_name":"keratin associated protein 3-2 [Source:HGNC Symbol;Acc:HGNC:16779]","synonyms":"KAP3.2","biotype":"protein_coding","ncbi_id":"83897","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":40999320,"end":41000021,"strand":-1,"description":"keratin associated protein 3-2 [Source:HGNC Symbol;Acc:HGNC:16779]"}, {"versioned_ensembl_gene_id":"ENSG00000251300.1","gene_symbol":"AC104596.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143045086,"end":143045878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232350.1","gene_symbol":"AC244250.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22689831,"end":22689978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167695.14","gene_symbol":"FAM57A","gene_name":"family with sequence similarity 57 member A [Source:HGNC Symbol;Acc:HGNC:29646]","synonyms":"FLJ22282,CT120","biotype":"protein_coding","ncbi_id":"79850","summary":"The protein encoded by this gene is a membrane-associated protein that promotes lung carcinogenesis. The encoded protein may be involved in amino acid transport and glutathione metabolism since it can interact with a solute carrier family member (SLC3A2) and an isoform of gamma-glutamyltranspeptidase-like 3. An alternatively spliced variant encoding a protein that lacks a 32 aa internal segment showed the opposite effect, inhibiting lung cancer cell growth. Knockdown of this gene also inhibited lung carcinogenesis and tumor cell growth. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":732412,"end":742972,"strand":1,"description":"family with sequence similarity 57 member A [Source:HGNC Symbol;Acc:HGNC:29646]"}, {"versioned_ensembl_gene_id":"ENSG00000238081.1","gene_symbol":"AC099063.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89289676,"end":89290337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148672.8","gene_symbol":"GLUD1","gene_name":"glutamate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:4335]","synonyms":"GLUD,GDH","biotype":"protein_coding","ncbi_id":"2746","summary":"This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X. [provided by RefSeq, Jan 2016]","start":87050486,"end":87094866,"strand":-1,"description":"glutamate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:4335]"}, {"versioned_ensembl_gene_id":"ENSG00000242154.1","gene_symbol":"AC004884.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105304277,"end":105306642,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257069.6","gene_symbol":"KCNK4-TEX40","gene_name":"KCNK4-TEX40 readthrough [Source:NCBI gene;Acc:106780802]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106780802","summary":"This locus represents naturally occurring readthrough transcription between the neighboring KCNK4 (potassium channel subfamily K member 4) and the downstream TEX40 (testis expressed 40) chromosome 11. The readthrough transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Nov 2015]","start":64291722,"end":64304769,"strand":1,"description":"KCNK4-TEX40 readthrough [Source:NCBI gene;Acc:106780802]"}, {"versioned_ensembl_gene_id":"ENSG00000268100.1","gene_symbol":"AC011493.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23492428,"end":23512656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163636.10","gene_symbol":"PSMD6","gene_name":"proteasome 26S subunit, non-ATPase 6 [Source:HGNC Symbol;Acc:HGNC:9564]","synonyms":"S10,Rpn7,p44S10,KIAA0107","biotype":"protein_coding","ncbi_id":"9861","summary":"This gene encodes a member of the protease subunit S10 family. The encoded protein is a subunit of the 26S proteasome which colocalizes with DNA damage foci and is involved in the ATP-dependent degradation of ubiquinated proteins. Alternative splicing results in multiple transcript variants [provided by RefSeq, Nov 2012]","start":64010549,"end":64024010,"strand":-1,"description":"proteasome 26S subunit, non-ATPase 6 [Source:HGNC Symbol;Acc:HGNC:9564]"}, {"versioned_ensembl_gene_id":"ENSG00000274554.1","gene_symbol":"AC083806.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116948738,"end":116951422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249572.1","gene_symbol":"AC034231.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33424025,"end":33440619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256733.1","gene_symbol":"AP003721.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61055737,"end":61067535,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225404.2","gene_symbol":"RPL26P34","gene_name":"ribosomal protein L26 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36249]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271470","summary":null,"start":24704338,"end":24704788,"strand":-1,"description":"ribosomal protein L26 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36249]"}, {"versioned_ensembl_gene_id":"ENSG00000106459.14","gene_symbol":"NRF1","gene_name":"nuclear respiratory factor 1 [Source:HGNC Symbol;Acc:HGNC:7996]","synonyms":"EWG,ALPHA-PAL","biotype":"protein_coding","ncbi_id":"4899","summary":"This gene encodes a protein that homodimerizes and functions as a transcription factor which activates the expression of some key metabolic genes regulating cellular growth and nuclear genes required for respiration, heme biosynthesis, and mitochondrial DNA transcription and replication. The protein has also been associated with the regulation of neurite outgrowth. Alternative splicing results in multiple transcript variants. Confusion has occurred in bibliographic databases due to the shared symbol of NRF1 for this gene and for \"nuclear factor (erythroid-derived 2)-like 1\" which has an official symbol of NFE2L1. [provided by RefSeq, May 2014]","start":129611714,"end":129757082,"strand":1,"description":"nuclear respiratory factor 1 [Source:HGNC Symbol;Acc:HGNC:7996]"}, {"versioned_ensembl_gene_id":"ENSG00000166024.13","gene_symbol":"R3HCC1L","gene_name":"R3H domain and coiled-coil containing 1 like [Source:HGNC Symbol;Acc:HGNC:23512]","synonyms":"C10orf28,PSORT,GIDRP86","biotype":"protein_coding","ncbi_id":"27291","summary":null,"start":98134624,"end":98244897,"strand":1,"description":"R3H domain and coiled-coil containing 1 like [Source:HGNC Symbol;Acc:HGNC:23512]"}, {"versioned_ensembl_gene_id":"ENSG00000211658.2","gene_symbol":"IGLV3-27","gene_name":"immunoglobulin lambda variable 3-27 [Source:HGNC Symbol;Acc:HGNC:5910]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28791","summary":null,"start":22668288,"end":22668806,"strand":1,"description":"immunoglobulin lambda variable 3-27 [Source:HGNC Symbol;Acc:HGNC:5910]"}, {"versioned_ensembl_gene_id":"ENSG00000253913.1","gene_symbol":"IGLV3-26","gene_name":"immunoglobulin lambda variable 3-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5909]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28792","summary":null,"start":22673152,"end":22673602,"strand":1,"description":"immunoglobulin lambda variable 3-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5909]"}, {"versioned_ensembl_gene_id":"ENSG00000188219.14","gene_symbol":"POTEE","gene_name":"POTE ankyrin domain family member E [Source:HGNC Symbol;Acc:HGNC:33895]","synonyms":"A26C1A,CT104.2,A26C1,POTE2gamma,POTE2,POTE-2","biotype":"protein_coding","ncbi_id":"445582","summary":null,"start":131218067,"end":131265278,"strand":1,"description":"POTE ankyrin domain family member E [Source:HGNC Symbol;Acc:HGNC:33895]"}, {"versioned_ensembl_gene_id":"ENSG00000174600.13","gene_symbol":"CMKLR1","gene_name":"chemerin chemokine-like receptor 1 [Source:HGNC Symbol;Acc:HGNC:2121]","synonyms":"RVER1","biotype":"protein_coding","ncbi_id":"1240","summary":null,"start":108288044,"end":108339341,"strand":-1,"description":"chemerin chemokine-like receptor 1 [Source:HGNC Symbol;Acc:HGNC:2121]"}, {"versioned_ensembl_gene_id":"ENSG00000284706.1","gene_symbol":"AC073869.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131335502,"end":131355769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147854.16","gene_symbol":"UHRF2","gene_name":"ubiquitin like with PHD and ring finger domains 2 [Source:HGNC Symbol;Acc:HGNC:12557]","synonyms":"URF2,TDRD23,RNF107,NIRF,MGC33463","biotype":"protein_coding","ncbi_id":"115426","summary":"This gene encodes a nuclear protein which is involved in cell-cycle regulation. The encoded protein is a ubiquitin-ligase capable of ubiquinating PCNP (PEST-containing nuclear protein), and together they may play a role in tumorigenesis. The encoded protein contains an NIRF_N domain, a PHD finger, a set- and ring-associated (SRA) domain, and a RING finger domain and several of these domains have been shown to be essential for the regulation of cell proliferation. This protein may also have a role in intranuclear degradation of polyglutamine aggregates. Alternative splicing results in multiple transcript variants some of which are non-protein coding. [provided by RefSeq, Feb 2012]","start":6413151,"end":6507054,"strand":1,"description":"ubiquitin like with PHD and ring finger domains 2 [Source:HGNC Symbol;Acc:HGNC:12557]"}, {"versioned_ensembl_gene_id":"ENSG00000282996.1","gene_symbol":"AC022021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28303300,"end":28307658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250770.3","gene_symbol":"AC005865.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3296202,"end":3366122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214541.3","gene_symbol":"RPS4XP3","gene_name":"ribosomal protein S4X pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16251]","synonyms":"RPS4P3,RPS4L,dJ843L14.2","biotype":"processed_pseudogene","ncbi_id":"128580","summary":null,"start":56601701,"end":56602113,"strand":1,"description":"ribosomal protein S4X pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16251]"}, {"versioned_ensembl_gene_id":"ENSG00000236908.2","gene_symbol":"AC005865.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3318718,"end":3325343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130150.11","gene_symbol":"MOSPD2","gene_name":"motile sperm domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28381]","synonyms":"MGC26706","biotype":"protein_coding","ncbi_id":"158747","summary":null,"start":14873441,"end":14922327,"strand":1,"description":"motile sperm domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28381]"}, {"versioned_ensembl_gene_id":"ENSG00000251485.1","gene_symbol":"AC068134.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":232343116,"end":232343903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274287.4","gene_symbol":"SCRIB","gene_name":"scribbled planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:30377]","synonyms":"Vartul,SCRB1,KIAA0147","biotype":"protein_coding","ncbi_id":"23513","summary":"This gene encodes a protein that was identified as being similar to the Drosophila scribble protein. The mammalian protein is involved in tumor suppression pathways. As a scaffold protein involved in cell polarization processes, this protein binds to many other proteins. The encoded protein binds to papillomavirus E6 protein via its PDZ domain and the C-terminus of E6. Two alternatively spliced transcript variants that encode different protein isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":143777927,"end":143802386,"strand":-1,"description":"scribbled planar cell polarity protein [Source:HGNC Symbol;Acc:HGNC:30377]"}, {"versioned_ensembl_gene_id":"ENSG00000281654.1","gene_symbol":"AC233280.14","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079101.16","gene_symbol":"CLUL1","gene_name":"clusterin like 1 [Source:HGNC Symbol;Acc:HGNC:2096]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27098","summary":null,"start":596988,"end":650334,"strand":1,"description":"clusterin like 1 [Source:HGNC Symbol;Acc:HGNC:2096]"}, {"versioned_ensembl_gene_id":"ENSG00000278202.1","gene_symbol":"AC243919.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":82418651,"end":82434235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137338.5","gene_symbol":"PGBD1","gene_name":"piggyBac transposable element derived 1 [Source:HGNC Symbol;Acc:HGNC:19398]","synonyms":"SCAND4,HUCEP-4,dJ874C20.4","biotype":"protein_coding","ncbi_id":"84547","summary":"The piggyBac family of proteins, found in diverse animals, are transposases related to the transposase of the canonical piggyBac transposon from the moth, Trichoplusia ni. This family also includes genes in several genomes, including human, that appear to have been derived from the piggyBac transposons. This gene belongs to the subfamily of piggyBac transposable element derived (PGBD) genes. The PGBD proteins appear to be novel, with no obvious relationship to other transposases, or other known protein families. This gene product is specifically expressed in the brain, however, its exact function is not known. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, May 2010]","start":28281572,"end":28302549,"strand":1,"description":"piggyBac transposable element derived 1 [Source:HGNC Symbol;Acc:HGNC:19398]"}, {"versioned_ensembl_gene_id":"ENSG00000238057.8","gene_symbol":"ZEB2-AS1","gene_name":"ZEB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37149]","synonyms":"ZEB2NAT,ZEB2AS,ZEB2-AS","biotype":"antisense_RNA","ncbi_id":"100303491","summary":"This gene produces a spliced long non-coding RNA which is a natural antisense transcript corresponding to the 5' UTR of zinc finger E-box binding homeobox 2 (ZEB2). It is thought that this transcript may be involved in the regulation of ZEB2 expression, and may play a role in the progression of bladder cancer. [provided by RefSeq, Aug 2015]","start":144518097,"end":144521477,"strand":1,"description":"ZEB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37149]"}, {"versioned_ensembl_gene_id":"ENSG00000188379.6","gene_symbol":"IFNA2","gene_name":"interferon alpha 2 [Source:HGNC Symbol;Acc:HGNC:5423]","synonyms":"IFNA,IFN-alphaA","biotype":"protein_coding","ncbi_id":"3440","summary":"This gene is a member of the alpha interferon gene cluster on chromosome 9. The encoded cytokine is a member of the type I interferon family that is produced in response to viral infection as a key part of the innate immune response with potent antiviral, antiproliferative and immunomodulatory properties. This cytokine, like other type I interferons, binds a plasma membrane receptor made of IFNAR1 and IFNAR2 that is ubiquitously expressed, and thus is able to act on virtually all body cells. The encoded protein is effective in reducing the symptoms and duration of the common cold and in treating many types of cancer, including some hematological malignancies and solid tumors. A deficiency of type I interferon in the blood is thought to be a hallmark of severe COVID-19 and may provide a rationale for a combined therapeutic approach. [provided by RefSeq, Aug 2020]","start":21384254,"end":21385388,"strand":-1,"description":"interferon alpha 2 [Source:HGNC Symbol;Acc:HGNC:5423]"}, {"versioned_ensembl_gene_id":"ENSG00000197978.9","gene_symbol":"GOLGA6L9","gene_name":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]","synonyms":"GOLGA6L20","biotype":"protein_coding","ncbi_id":"440295","summary":null,"start":82430018,"end":82439153,"strand":1,"description":"golgin A6 family-like 9 [Source:HGNC Symbol;Acc:HGNC:37229]"}, {"versioned_ensembl_gene_id":"ENSG00000237351.1","gene_symbol":"AL513366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47156638,"end":47158199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227033.1","gene_symbol":"AC019130.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":231978488,"end":232015720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259633.1","gene_symbol":"UBE2Q2P8","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49521]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421771","summary":null,"start":84255913,"end":84256014,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49521]"}, {"versioned_ensembl_gene_id":"ENSG00000284308.1","gene_symbol":"C2orf81","gene_name":"chromosome 2 open reading frame 81 [Source:HGNC Symbol;Acc:HGNC:34350]","synonyms":"LOC388963,hCG40743","biotype":"protein_coding","ncbi_id":"388963","summary":null,"start":74414176,"end":74421591,"strand":-1,"description":"chromosome 2 open reading frame 81 [Source:HGNC Symbol;Acc:HGNC:34350]"}, {"versioned_ensembl_gene_id":"ENSG00000284500.1","gene_symbol":"AC134980.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":21990061,"end":22125546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259435.2","gene_symbol":"OR4N3P","gene_name":"olfactory receptor family 4 subfamily N member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15374]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390539","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":22125618,"end":22126435,"strand":1,"description":"olfactory receptor family 4 subfamily N member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15374]"}, {"versioned_ensembl_gene_id":"ENSG00000268803.1","gene_symbol":"AC114797.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69215908,"end":69216635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236610.1","gene_symbol":"SOCS5P1","gene_name":"suppressor of cytokine signaling 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44597]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420754","summary":null,"start":86216785,"end":86217733,"strand":-1,"description":"suppressor of cytokine signaling 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44597]"}, {"versioned_ensembl_gene_id":"ENSG00000282764.1","gene_symbol":"KSR1P1","gene_name":"kinase suppressor of ras 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479050","summary":null,"start":42149310,"end":42149549,"strand":-1,"description":"kinase suppressor of ras 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44977]"}, {"versioned_ensembl_gene_id":"ENSG00000227785.1","gene_symbol":"AC092013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85636013,"end":85636344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114626.17","gene_symbol":"ABTB1","gene_name":"ankyrin repeat and BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18275]","synonyms":"EF1ABP,BTBD21,Btb3,BPOZ","biotype":"protein_coding","ncbi_id":"80325","summary":"This gene encodes a protein with an ankyrin repeat region and two BTB/POZ domains, which are thought to be involved in protein-protein interactions. Expression of this gene is activated by the phosphatase and tensin homolog, a tumor suppressor. Alternate splicing results in three transcript variants. [provided by RefSeq, Mar 2010]","start":127672935,"end":127680920,"strand":1,"description":"ankyrin repeat and BTB domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18275]"}, {"versioned_ensembl_gene_id":"ENSG00000278891.1","gene_symbol":"AC105101.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48147634,"end":48150864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144535.19","gene_symbol":"DIS3L2","gene_name":"DIS3 like 3'-5' exoribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:28648]","synonyms":"MGC42174,FLJ36974,FAM6A","biotype":"protein_coding","ncbi_id":"129563","summary":"The protein encoded by this gene is similar in sequence to 3'/5' exonucleolytic subunits of the RNA exosome. The exosome is a large multimeric ribonucleotide complex responsible for degrading various RNA substrates. Several transcript variants, some protein-coding and some not, have been found for this gene. [provided by RefSeq, Mar 2012]","start":231961245,"end":232344350,"strand":1,"description":"DIS3 like 3'-5' exoribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:28648]"}, {"versioned_ensembl_gene_id":"ENSG00000267069.1","gene_symbol":"AP005264.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12288308,"end":12291488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259614.2","gene_symbol":"AC087477.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96388214,"end":96389056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256340.8","gene_symbol":"ABCC6P1","gene_name":"ATP binding cassette subfamily C member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33352]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653190","summary":null,"start":18571162,"end":18598328,"strand":1,"description":"ATP binding cassette subfamily C member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33352]"}, {"versioned_ensembl_gene_id":"ENSG00000280302.1","gene_symbol":"AP005264.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":12279427,"end":12282739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283773.1","gene_symbol":"AL137798.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16642767,"end":16643109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229723.1","gene_symbol":"LINC01054","gene_name":"long intergenic non-protein coding RNA 1054 [Source:HGNC Symbol;Acc:HGNC:49048]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355150","summary":null,"start":114329559,"end":114333948,"strand":-1,"description":"long intergenic non-protein coding RNA 1054 [Source:HGNC Symbol;Acc:HGNC:49048]"}, {"versioned_ensembl_gene_id":"ENSG00000168461.12","gene_symbol":"RAB31","gene_name":"RAB31, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9771]","synonyms":"Rab22B","biotype":"protein_coding","ncbi_id":"11031","summary":"Small GTP-binding proteins of the RAB family, such as RAB31, play essential roles in vesicle and granule targeting (Bao et al., 2002 [PubMed 11784320]).[supplied by OMIM, Jul 2009]","start":9708165,"end":9862551,"strand":1,"description":"RAB31, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9771]"}, {"versioned_ensembl_gene_id":"ENSG00000129214.14","gene_symbol":"SHBG","gene_name":"sex hormone binding globulin [Source:HGNC Symbol;Acc:HGNC:10839]","synonyms":"TEBG,MGC138391,MGC126834,ABP","biotype":"protein_coding","ncbi_id":"6462","summary":"This gene encodes a steroid binding protein that was first described as a plasma protein secreted by the liver but is now thought to participate in the regulation of steroid responses. The encoded protein transports androgens and estrogens in the blood, binding each steroid molecule as a dimer formed from identical or nearly identical monomers. Polymorphisms in this gene have been associated with polycystic ovary syndrome and type 2 diabetes mellitus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":7613946,"end":7633383,"strand":1,"description":"sex hormone binding globulin [Source:HGNC Symbol;Acc:HGNC:10839]"}, {"versioned_ensembl_gene_id":"ENSG00000223684.1","gene_symbol":"IFNWP18","gene_name":"interferon omega 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:5450]","synonyms":"pseudo-IFN-alpha-m","biotype":"unprocessed_pseudogene","ncbi_id":"360001","summary":null,"start":21209189,"end":21209779,"strand":-1,"description":"interferon omega 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:5450]"}, {"versioned_ensembl_gene_id":"ENSG00000186803.3","gene_symbol":"IFNA10","gene_name":"interferon alpha 10 [Source:HGNC Symbol;Acc:HGNC:5418]","synonyms":"IFN-alphaC","biotype":"protein_coding","ncbi_id":"3446","summary":"This gene encodes a protein that belongs to the type I interferon family of proteins, and is located in a cluster of alpha interferon genes on chromosome 9. Interferons are small regulatory molecules that function in cell signaling in response to viruses and other pathogens or tumor cells. This gene is intronless and the encoded protein is secreted. [provided by RefSeq, Aug 2013]","start":21206181,"end":21207143,"strand":-1,"description":"interferon alpha 10 [Source:HGNC Symbol;Acc:HGNC:5418]"}, {"versioned_ensembl_gene_id":"ENSG00000138398.15","gene_symbol":"PPIG","gene_name":"peptidylprolyl isomerase G [Source:HGNC Symbol;Acc:HGNC:14650]","synonyms":"SRCyp,SCAF10,CARS-Cyp","biotype":"protein_coding","ncbi_id":"9360","summary":null,"start":169584340,"end":169641406,"strand":1,"description":"peptidylprolyl isomerase G [Source:HGNC Symbol;Acc:HGNC:14650]"}, {"versioned_ensembl_gene_id":"ENSG00000232430.1","gene_symbol":"RPL31P15","gene_name":"ribosomal protein L31 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270984","summary":null,"start":182788098,"end":182788435,"strand":1,"description":"ribosomal protein L31 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36339]"}, {"versioned_ensembl_gene_id":"ENSG00000267341.1","gene_symbol":"AC100843.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62372894,"end":62378130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120948.16","gene_symbol":"TARDBP","gene_name":"TAR DNA binding protein [Source:HGNC Symbol;Acc:HGNC:11571]","synonyms":"TDP-43,ALS10","biotype":"protein_coding","ncbi_id":"23435","summary":"HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expression by the transactivator Tat is dependent on an RNA regulatory element (TAR) located downstream of the transcription initiation site. The protein encoded by this gene is a transcriptional repressor that binds to chromosomally integrated TAR DNA and represses HIV-1 transcription. In addition, this protein regulates alternate splicing of the CFTR gene. A similar pseudogene is present on chromosome 20. [provided by RefSeq, Jul 2008]","start":11012344,"end":11026420,"strand":1,"description":"TAR DNA binding protein [Source:HGNC Symbol;Acc:HGNC:11571]"}, {"versioned_ensembl_gene_id":"ENSG00000261239.6","gene_symbol":"ANKRD26P1","gene_name":"ankyrin repeat domain 26 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32955]","synonyms":"FLJ43980","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"124149","summary":null,"start":46469341,"end":46569097,"strand":-1,"description":"ankyrin repeat domain 26 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32955]"}, {"versioned_ensembl_gene_id":"ENSG00000272004.1","gene_symbol":"FO704657.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1659325,"end":1662602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176194.17","gene_symbol":"CIDEA","gene_name":"cell death-inducing DFFA-like effector a [Source:HGNC Symbol;Acc:HGNC:1976]","synonyms":"CIDE-A","biotype":"protein_coding","ncbi_id":"1149","summary":"This gene encodes the homolog of the mouse protein Cidea that has been shown to activate apoptosis. This activation of apoptosis is inhibited by the DNA fragmentation factor DFF45 but not by caspase inhibitors. Mice that lack functional Cidea have higher metabolic rates, higher lipolysis in brown adipose tissue and higher core body temperatures when subjected to cold. These mice are also resistant to diet-induced obesity and diabetes. This suggests that in mice this gene product plays a role in thermogenesis and lipolysis. Alternatively spliced transcripts have been identified. [provided by RefSeq, Aug 2010]","start":12254319,"end":12277595,"strand":1,"description":"cell death-inducing DFFA-like effector a [Source:HGNC Symbol;Acc:HGNC:1976]"}, {"versioned_ensembl_gene_id":"ENSG00000269737.2","gene_symbol":"AL691432.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":1671990,"end":1674397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255174.1","gene_symbol":"AC107918.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11999087,"end":11999468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260882.1","gene_symbol":"AC026458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5078168,"end":5078605,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161956.12","gene_symbol":"SENP3","gene_name":"SUMO1/sentrin/SMT3 specific peptidase 3 [Source:HGNC Symbol;Acc:HGNC:17862]","synonyms":"Ulp1,SSP3,SMT3IP1,DKFZp762A152,DKFZP586K0919","biotype":"protein_coding","ncbi_id":"26168","summary":"The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1; MIM 601912) is required for numerous biologic processes. SUMO-specific proteases, such as SENP3, are responsible for the initial processing of SUMO precursors to generate a C-terminal diglycine motif required for the conjugation reaction. They also have isopeptidase activity for the removal of SUMO from high molecular mass SUMO conjugates (Di Bacco et al., 2006 [PubMed 16738315]).[supplied by OMIM, Jun 2009]","start":7561875,"end":7571969,"strand":1,"description":"SUMO1/sentrin/SMT3 specific peptidase 3 [Source:HGNC Symbol;Acc:HGNC:17862]"}, {"versioned_ensembl_gene_id":"ENSG00000103174.11","gene_symbol":"NAGPA","gene_name":"N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:17378]","synonyms":"UCE,APAA","biotype":"protein_coding","ncbi_id":"51172","summary":"Hydrolases are transported to lysosomes after binding to mannose 6-phosphate receptors in the trans-Golgi network. This gene encodes the enzyme that catalyzes the second step in the formation of the mannose 6-phosphate recognition marker on lysosomal hydrolases. Commonly known as 'uncovering enzyme' or UCE, this enzyme removes N-acetyl-D-glucosamine (GlcNAc) residues from GlcNAc-alpha-P-mannose moieties and thereby produces the recognition marker. The encoded preproprotein is proteolytically processed by furin to generate the mature enzyme, a homotetramer of two disulfide-linked homodimers. Mutations in this gene are associated with developmental stuttering in human patients. [provided by RefSeq, Oct 2015]","start":5024844,"end":5034141,"strand":-1,"description":"N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:HGNC:17378]"}, {"versioned_ensembl_gene_id":"ENSG00000242854.1","gene_symbol":"DNM1P24","gene_name":"dynamin 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35171]","synonyms":"DNM1DN15@,DNM1DN15-1","biotype":"unprocessed_pseudogene","ncbi_id":"100216505","summary":null,"start":24179316,"end":24183505,"strand":-1,"description":"dynamin 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35171]"}, {"versioned_ensembl_gene_id":"ENSG00000225439.2","gene_symbol":"BOLA3-AS1","gene_name":"BOLA3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:42922]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507171","summary":null,"start":74148009,"end":74150061,"strand":1,"description":"BOLA3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:42922]"}, {"versioned_ensembl_gene_id":"ENSG00000230977.1","gene_symbol":"AC023274.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24182477,"end":24183071,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244231.1","gene_symbol":"CSPG4P2Y","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:32424]","synonyms":"CSPG4P2,CSPG4LYP2","biotype":"processed_transcript","ncbi_id":"84664","summary":"There are two copies of this pseudogene within the P1 palindrome on chromosome Y. This record represents the more centromeric copy. This gene is identical to the transcribed locus CSPG4P1Y, GeneID 114758, but is represented as non-transcribed because there is no representative transcript available in a public sequence database. [provided by RefSeq, Feb 2011]","start":24183434,"end":24187231,"strand":-1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:32424]"}, {"versioned_ensembl_gene_id":"ENSG00000172342.5","gene_symbol":"CSPG4P3Y","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:38111]","synonyms":"CSPG4P6Y,CSPG4P3","biotype":"unprocessed_pseudogene","ncbi_id":"100287261","summary":null,"start":24186509,"end":24191870,"strand":-1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:38111]"}, {"versioned_ensembl_gene_id":"ENSG00000179270.6","gene_symbol":"C2orf71","gene_name":"chromosome 2 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34383]","synonyms":"RP54,FLJ34931","biotype":"protein_coding","ncbi_id":"388939","summary":"The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]","start":29060976,"end":29074261,"strand":-1,"description":"chromosome 2 open reading frame 71 [Source:HGNC Symbol;Acc:HGNC:34383]"}, {"versioned_ensembl_gene_id":"ENSG00000254507.2","gene_symbol":"DEFB131E","gene_name":"defensin beta 131E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:39765]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":12003400,"end":12004082,"strand":-1,"description":"defensin beta 131E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:39765]"}, {"versioned_ensembl_gene_id":"ENSG00000130988.12","gene_symbol":"RGN","gene_name":"regucalcin [Source:HGNC Symbol;Acc:HGNC:9989]","synonyms":"SMP30,RC","biotype":"protein_coding","ncbi_id":"9104","summary":"The protein encoded by this gene is a highly conserved, calcium-binding protein, that is preferentially expressed in the liver and kidney. It may have an important role in calcium homeostasis. Studies in rat indicate that this protein may also play a role in aging, as it shows age-associated down-regulation. This gene is part of a gene cluster on chromosome Xp11.3-Xp11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":47078355,"end":47093314,"strand":1,"description":"regucalcin [Source:HGNC Symbol;Acc:HGNC:9989]"}, {"versioned_ensembl_gene_id":"ENSG00000135119.14","gene_symbol":"RNFT2","gene_name":"ring finger protein, transmembrane 2 [Source:HGNC Symbol;Acc:HGNC:25905]","synonyms":"FLJ14627,TMEM118","biotype":"protein_coding","ncbi_id":"84900","summary":null,"start":116738178,"end":116853631,"strand":1,"description":"ring finger protein, transmembrane 2 [Source:HGNC Symbol;Acc:HGNC:25905]"}, {"versioned_ensembl_gene_id":"ENSG00000003096.14","gene_symbol":"KLHL13","gene_name":"kelch like family member 13 [Source:HGNC Symbol;Acc:HGNC:22931]","synonyms":"KIAA1309,FLJ10262,BKLHD2","biotype":"protein_coding","ncbi_id":"90293","summary":"This gene encodes a BTB and kelch domain containing protein and belongs to the kelch repeat domain containing superfamily of proteins. The encoded protein functions as an adaptor protein that complexes with Cullin 3 and other proteins to form the Cullin 3-based E3 ubiquitin-protein ligase complex. This complex is necessary for proper chromosome segregation and completion of cytokinesis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":117897813,"end":118117340,"strand":-1,"description":"kelch like family member 13 [Source:HGNC Symbol;Acc:HGNC:22931]"}, {"versioned_ensembl_gene_id":"ENSG00000115761.15","gene_symbol":"NOL10","gene_name":"nucleolar protein 10 [Source:HGNC Symbol;Acc:HGNC:25862]","synonyms":"PQBP5,FLJ14075","biotype":"protein_coding","ncbi_id":"79954","summary":null,"start":10570766,"end":10689987,"strand":-1,"description":"nucleolar protein 10 [Source:HGNC Symbol;Acc:HGNC:25862]"}, {"versioned_ensembl_gene_id":"ENSG00000278862.1","gene_symbol":"AC092724.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":77657174,"end":77660570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261102.2","gene_symbol":"ATP5J2P6","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654486","summary":null,"start":66414933,"end":66415198,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33612]"}, {"versioned_ensembl_gene_id":"ENSG00000261351.2","gene_symbol":"AC116913.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66488658,"end":66492109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181544.13","gene_symbol":"FANCB","gene_name":"Fanconi anemia complementation group B [Source:HGNC Symbol;Acc:HGNC:3583]","synonyms":"FLJ34064,FAB,FAAP95","biotype":"protein_coding","ncbi_id":"2187","summary":"This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]","start":14843407,"end":14873069,"strand":-1,"description":"Fanconi anemia complementation group B [Source:HGNC Symbol;Acc:HGNC:3583]"}, {"versioned_ensembl_gene_id":"ENSG00000169032.9","gene_symbol":"MAP2K1","gene_name":"mitogen-activated protein kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6840]","synonyms":"PRKMK1,MEK1,MAPKK1","biotype":"protein_coding","ncbi_id":"5604","summary":"The protein encoded by this gene is a member of the dual specificity protein kinase family, which acts as a mitogen-activated protein (MAP) kinase kinase. MAP kinases, also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals. This protein kinase lies upstream of MAP kinases and stimulates the enzymatic activity of MAP kinases upon wide variety of extra- and intracellular signals. As an essential component of MAP kinase signal transduction pathway, this kinase is involved in many cellular processes such as proliferation, differentiation, transcription regulation and development. [provided by RefSeq, Jul 2008]","start":66386817,"end":66492312,"strand":1,"description":"mitogen-activated protein kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6840]"}, {"versioned_ensembl_gene_id":"ENSG00000259357.2","gene_symbol":"AL590133.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150965245,"end":150966256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143418.19","gene_symbol":"CERS2","gene_name":"ceramide synthase 2 [Source:HGNC Symbol;Acc:HGNC:14076]","synonyms":"SP260,LASS2,FLJ10243","biotype":"protein_coding","ncbi_id":"29956","summary":"This gene encodes a protein that has sequence similarity to yeast longevity assurance gene 1. Mutation or overexpression of the related gene in yeast has been shown to alter yeast lifespan. The human protein may play a role in the regulation of cell growth. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":150960583,"end":150975004,"strand":-1,"description":"ceramide synthase 2 [Source:HGNC Symbol;Acc:HGNC:14076]"}, {"versioned_ensembl_gene_id":"ENSG00000258167.1","gene_symbol":"AC107023.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40395853,"end":40443847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205592.13","gene_symbol":"MUC19","gene_name":"mucin 19, oligomeric [Source:HGNC Symbol;Acc:HGNC:14362]","synonyms":"FLJ35746","biotype":"processed_transcript","ncbi_id":"283463","summary":"This gene encodes a member of the gel-forming mucin protein family. Mucin family members are glycoproteins that have tandem repeats which are extensively O-glycosylated. The structural features of mucin proteins are responsible for the gel-like properties of mucus. The encoded protein may be involved in disruption of the ocular surface in Sjogren syndrome. [provided by RefSeq, Apr 2014]","start":40393395,"end":40570832,"strand":1,"description":"mucin 19, oligomeric [Source:HGNC Symbol;Acc:HGNC:14362]"}, {"versioned_ensembl_gene_id":"ENSG00000215197.4","gene_symbol":"PGAM4P1","gene_name":"phosphoglycerate mutase family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42465]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421178","summary":null,"start":54671985,"end":54672638,"strand":1,"description":"phosphoglycerate mutase family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42465]"}, {"versioned_ensembl_gene_id":"ENSG00000237425.1","gene_symbol":"RPSAP2","gene_name":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]","synonyms":"LAMR1P2,bA60E24.1","biotype":"processed_pseudogene","ncbi_id":"442181","summary":null,"start":28732017,"end":28732904,"strand":1,"description":"ribosomal protein SA pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18771]"}, {"versioned_ensembl_gene_id":"ENSG00000198832.10","gene_symbol":"SELENOM","gene_name":"selenoprotein M [Source:HGNC Symbol;Acc:HGNC:30397]","synonyms":"SEPM,SELM","biotype":"protein_coding","ncbi_id":"140606","summary":"The protein encoded by this gene belongs to the selenoprotein M/SEP15 family. The exact function of this protein is not known. It is localized in the perinuclear region, is highly expressed in the brain, and may be involved in neurodegenerative disorders. Transgenic mice with targeted deletion of this gene exhibit increased weight gain, suggesting a role for this gene in the regulation of body weight and energy metabolism. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. [provided by RefSeq, Dec 2016]","start":31104772,"end":31120069,"strand":-1,"description":"selenoprotein M [Source:HGNC Symbol;Acc:HGNC:30397]"}, {"versioned_ensembl_gene_id":"ENSG00000149806.10","gene_symbol":"FAU","gene_name":"FAU, ubiquitin like and ribosomal protein S30 fusion [Source:HGNC Symbol;Acc:HGNC:3597]","synonyms":"S30,RPS30,MNSFbeta,Fubi,Fub1,FLJ22986,asr1","biotype":"protein_coding","ncbi_id":"2197","summary":"This gene is the cellular homolog of the fox sequence in the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV). It encodes a fusion protein consisting of the ubiquitin-like protein fubi at the N terminus and ribosomal protein S30 at the C terminus. It has been proposed that the fusion protein is post-translationally processed to generate free fubi and free ribosomal protein S30. Fubi is a member of the ubiquitin family, and ribosomal protein S30 belongs to the S30E family of ribosomal proteins. Whereas the function of fubi is currently unknown, ribosomal protein S30 is a component of the 40S subunit of the cytoplasmic ribosome and displays antimicrobial activity. Pseudogenes derived from this gene are present in the genome. Similar to ribosomal protein S30, ribosomal proteins S27a and L40 are synthesized as fusion proteins with ubiquitin. [provided by RefSeq, Nov 2014]","start":65120628,"end":65122473,"strand":-1,"description":"FAU, ubiquitin like and ribosomal protein S30 fusion [Source:HGNC Symbol;Acc:HGNC:3597]"}, {"versioned_ensembl_gene_id":"ENSG00000144381.16","gene_symbol":"HSPD1","gene_name":"heat shock protein family D (Hsp60) member 1 [Source:HGNC Symbol;Acc:HGNC:5261]","synonyms":"SPG13,HSP60,GroEL","biotype":"protein_coding","ncbi_id":"3329","summary":"This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010]","start":197486581,"end":197516737,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 [Source:HGNC Symbol;Acc:HGNC:5261]"}, {"versioned_ensembl_gene_id":"ENSG00000226801.2","gene_symbol":"OSTCP8","gene_name":"oligosaccharyltransferase complex subunit pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42869]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874388","summary":null,"start":33968071,"end":33968518,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42869]"}, {"versioned_ensembl_gene_id":"ENSG00000137073.21","gene_symbol":"UBAP2","gene_name":"ubiquitin associated protein 2 [Source:HGNC Symbol;Acc:HGNC:14185]","synonyms":"KIAA1491,FLJ22435,bA176F3.5","biotype":"protein_coding","ncbi_id":"55833","summary":"The protein encoded by this gene contains a UBA (ubiquitin associated) domain, which is characteristic of proteins that function in the ubiquitination pathway. This gene may show increased expression in the adrenal gland and lymphatic tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":33921693,"end":34048949,"strand":-1,"description":"ubiquitin associated protein 2 [Source:HGNC Symbol;Acc:HGNC:14185]"}, {"versioned_ensembl_gene_id":"ENSG00000261790.1","gene_symbol":"AC005606.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1984877,"end":1990357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259463.1","gene_symbol":"AC020661.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41011597,"end":41013300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264772.6","gene_symbol":"AC016876.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7572826,"end":7582024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183751.14","gene_symbol":"TBL3","gene_name":"transducin beta like 3 [Source:HGNC Symbol;Acc:HGNC:11587]","synonyms":"UTP13,SAZD","biotype":"protein_coding","ncbi_id":"10607","summary":"The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This gene has multiple polyadenylation sites. It might have multiple alternatively spliced transcript variants but the variants have not been fully described yet. [provided by RefSeq, Jul 2008]","start":1972037,"end":1982933,"strand":1,"description":"transducin beta like 3 [Source:HGNC Symbol;Acc:HGNC:11587]"}, {"versioned_ensembl_gene_id":"ENSG00000163032.11","gene_symbol":"VSNL1","gene_name":"visinin like 1 [Source:HGNC Symbol;Acc:HGNC:12722]","synonyms":"VILIP-1,VILIP,HUVISL1,HPCAL3,HLP3","biotype":"protein_coding","ncbi_id":"7447","summary":"This gene is a member of the visinin/recoverin subfamily of neuronal calcium sensor proteins. The encoded protein is strongly expressed in granule cells of the cerebellum where it associates with membranes in a calcium-dependent manner and modulates intracellular signaling pathways of the central nervous system by directly or indirectly regulating the activity of adenylyl cyclase. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":17539126,"end":17657018,"strand":1,"description":"visinin like 1 [Source:HGNC Symbol;Acc:HGNC:12722]"}, {"versioned_ensembl_gene_id":"ENSG00000129245.11","gene_symbol":"FXR2","gene_name":"FMR1 autosomal homolog 2 [Source:HGNC Symbol;Acc:HGNC:4024]","synonyms":"FMR1L2","biotype":"protein_coding","ncbi_id":"9513","summary":"The protein encoded by this gene is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This encoded protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X cognitive disability syndrome. [provided by RefSeq, Jul 2008]","start":7591230,"end":7614871,"strand":-1,"description":"FMR1 autosomal homolog 2 [Source:HGNC Symbol;Acc:HGNC:4024]"}, {"versioned_ensembl_gene_id":"ENSG00000144644.14","gene_symbol":"GADL1","gene_name":"glutamate decarboxylase like 1 [Source:HGNC Symbol;Acc:HGNC:27949]","synonyms":null,"biotype":"protein_coding","ncbi_id":"339896","summary":null,"start":30726200,"end":30894765,"strand":-1,"description":"glutamate decarboxylase like 1 [Source:HGNC Symbol;Acc:HGNC:27949]"}, {"versioned_ensembl_gene_id":"ENSG00000275467.1","gene_symbol":"AC083806.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116801023,"end":116801477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239374.1","gene_symbol":"AC090013.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116755395,"end":116755874,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101407.12","gene_symbol":"TTI1","gene_name":"TELO2 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29029]","synonyms":"smg-10,KIAA0406","biotype":"protein_coding","ncbi_id":"9675","summary":null,"start":37983007,"end":38033468,"strand":-1,"description":"TELO2 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:29029]"}, {"versioned_ensembl_gene_id":"ENSG00000242353.1","gene_symbol":"RPL12P30","gene_name":"ribosomal protein L12 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271405","summary":null,"start":30368148,"end":30368646,"strand":1,"description":"ribosomal protein L12 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35970]"}, {"versioned_ensembl_gene_id":"ENSG00000243404.2","gene_symbol":"AC011276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66446455,"end":66446777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225446.2","gene_symbol":"LINC01763","gene_name":"long intergenic non-protein coding RNA 1763 [Source:HGNC Symbol;Acc:HGNC:52554]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378854","summary":null,"start":90851759,"end":90855253,"strand":1,"description":"long intergenic non-protein coding RNA 1763 [Source:HGNC Symbol;Acc:HGNC:52554]"}, {"versioned_ensembl_gene_id":"ENSG00000230772.1","gene_symbol":"VN1R108P","gene_name":"vomeronasal 1 receptor 108 pseudogene [Source:HGNC Symbol;Acc:HGNC:37432]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312850","summary":null,"start":25734264,"end":25735093,"strand":1,"description":"vomeronasal 1 receptor 108 pseudogene [Source:HGNC Symbol;Acc:HGNC:37432]"}, {"versioned_ensembl_gene_id":"ENSG00000174446.12","gene_symbol":"SNAPC5","gene_name":"small nuclear RNA activating complex polypeptide 5 [Source:HGNC Symbol;Acc:HGNC:15484]","synonyms":"SNAP19","biotype":"protein_coding","ncbi_id":"10302","summary":"This gene encodes a subunit of the small nuclear RNA (snRNA)-activating protein complex that plays a role in the transcription of snRNA genes. This complex binds to the promoters of snRNA genes transcribed by either RNA polymerase II or III and recruits other regulatory factors to activate snRNA gene transcription. The encoded protein may play a role in stabilizing this complex. A pseudogene of this gene has been identified on chromosome 6. [provided by RefSeq, Jul 2016]","start":66490135,"end":66497813,"strand":-1,"description":"small nuclear RNA activating complex polypeptide 5 [Source:HGNC Symbol;Acc:HGNC:15484]"}, {"versioned_ensembl_gene_id":"ENSG00000171564.11","gene_symbol":"FGB","gene_name":"fibrinogen beta chain [Source:HGNC Symbol;Acc:HGNC:3662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2244","summary":"The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Fibrinogen serves key roles in hemostasis and antimicrobial host defense. Mutations in this gene lead to several disorders, including afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency. [provided by RefSeq, Aug 2020]","start":154562956,"end":154571086,"strand":1,"description":"fibrinogen beta chain [Source:HGNC Symbol;Acc:HGNC:3662]"}, {"versioned_ensembl_gene_id":"ENSG00000142444.6","gene_symbol":"TIMM29","gene_name":"translocase of inner mitochondrial membrane 29 [Source:HGNC Symbol;Acc:HGNC:25152]","synonyms":"C19orf52","biotype":"protein_coding","ncbi_id":"90580","summary":null,"start":10928733,"end":10933535,"strand":1,"description":"translocase of inner mitochondrial membrane 29 [Source:HGNC Symbol;Acc:HGNC:25152]"}, {"versioned_ensembl_gene_id":"ENSG00000235573.2","gene_symbol":"AC005005.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31113017,"end":31113396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116691.10","gene_symbol":"MIIP","gene_name":"migration and invasion inhibitory protein [Source:HGNC Symbol;Acc:HGNC:25715]","synonyms":"IIp45,FLJ12438","biotype":"protein_coding","ncbi_id":"60672","summary":"This gene encodes a protein that interacts with the oncogene protein insulin-like growth factor binding protein 2 and may function as an inhibitor of cell migration and invasion. This protein also interacts with the cell division protein 20 and may be involved in regulating mitotic progression. This protein may function as a tumor suppressor by inhibiting the growth or certain cancers. [provided by RefSeq, Sep 2011]","start":12019466,"end":12032045,"strand":1,"description":"migration and invasion inhibitory protein [Source:HGNC Symbol;Acc:HGNC:25715]"}, {"versioned_ensembl_gene_id":"ENSG00000275225.1","gene_symbol":"GU182354.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54754999,"end":54767347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275456.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803616,"end":54814523,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000235486.1","gene_symbol":"AC114755.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106369724,"end":106378247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234285.1","gene_symbol":"GAPDHP49","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:38555]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421189","summary":null,"start":222503883,"end":222504843,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:38555]"}, {"versioned_ensembl_gene_id":"ENSG00000259340.2","gene_symbol":"AC110588.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96551381,"end":96551517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227743.1","gene_symbol":"AC004875.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121643334,"end":121650360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229682.1","gene_symbol":"AC114755.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106368209,"end":106368876,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171310.10","gene_symbol":"CHST11","gene_name":"carbohydrate sulfotransferase 11 [Source:HGNC Symbol;Acc:HGNC:17422]","synonyms":"HSA269537,C4ST1,C4St-1,C4ST","biotype":"protein_coding","ncbi_id":"50515","summary":"The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. A chromosomal translocation involving this gene and IgH, t(12;14)(q23;q32), has been reported in a patient with B-cell chronic lymphocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":104455295,"end":104762014,"strand":1,"description":"carbohydrate sulfotransferase 11 [Source:HGNC Symbol;Acc:HGNC:17422]"}, {"versioned_ensembl_gene_id":"ENSG00000198523.5","gene_symbol":"PLN","gene_name":"phospholamban [Source:HGNC Symbol;Acc:HGNC:9080]","synonyms":"PLB,CMD1P","biotype":"protein_coding","ncbi_id":"5350","summary":"The protein encoded by this gene is found as a pentamer and is a major substrate for the cAMP-dependent protein kinase in cardiac muscle. The encoded protein is an inhibitor of cardiac muscle sarcoplasmic reticulum Ca(2+)-ATPase in the unphosphorylated state, but inhibition is relieved upon phosphorylation of the protein. The subsequent activation of the Ca(2+) pump leads to enhanced muscle relaxation rates, thereby contributing to the inotropic response elicited in heart by beta-agonists. The encoded protein is a key regulator of cardiac diastolic function. Mutations in this gene are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure, and also familial hypertrophic cardiomyopathy. [provided by RefSeq, Apr 2016]","start":118548298,"end":118560730,"strand":1,"description":"phospholamban [Source:HGNC Symbol;Acc:HGNC:9080]"}, {"versioned_ensembl_gene_id":"ENSG00000271874.1","gene_symbol":"AC025754.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34651457,"end":34651888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261803.1","gene_symbol":"LINC02140","gene_name":"long intergenic non-protein coding RNA 2140 [Source:HGNC Symbol;Acc:HGNC:53000]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996345","summary":null,"start":54366007,"end":54370699,"strand":-1,"description":"long intergenic non-protein coding RNA 2140 [Source:HGNC Symbol;Acc:HGNC:53000]"}, {"versioned_ensembl_gene_id":"ENSG00000235570.1","gene_symbol":"LINC00533","gene_name":"long intergenic non-protein coding RNA 533 [Source:HGNC Symbol;Acc:HGNC:18690]","synonyms":"C6orf39,C6orf38,bA373N24.1","biotype":"lincRNA","ncbi_id":"387055","summary":null,"start":28648286,"end":28649066,"strand":-1,"description":"long intergenic non-protein coding RNA 533 [Source:HGNC Symbol;Acc:HGNC:18690]"}, {"versioned_ensembl_gene_id":"ENSG00000206106.2","gene_symbol":"KRTAP22-2","gene_name":"keratin associated protein 22-2 [Source:HGNC Symbol;Acc:HGNC:37091]","synonyms":"KAP22.2","biotype":"protein_coding","ncbi_id":"100288287","summary":null,"start":30590105,"end":30590397,"strand":-1,"description":"keratin associated protein 22-2 [Source:HGNC Symbol;Acc:HGNC:37091]"}, {"versioned_ensembl_gene_id":"ENSG00000127603.24","gene_symbol":"MACF1","gene_name":"microtubule-actin crosslinking factor 1 [Source:HGNC Symbol;Acc:HGNC:13664]","synonyms":"MACF,KIAA1251,KIAA0465,FLJ46776,FLJ45612,ACF7,ABP620","biotype":"protein_coding","ncbi_id":"23499","summary":"This gene encodes a large protein containing numerous spectrin and leucine-rich repeat (LRR) domains. The encoded protein is a member of a family of proteins that form bridges between different cytoskeletal elements. This protein facilitates actin-microtubule interactions at the cell periphery and couples the microtubule network to cellular junctions. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, May 2013]","start":39081316,"end":39487177,"strand":1,"description":"microtubule-actin crosslinking factor 1 [Source:HGNC Symbol;Acc:HGNC:13664]"}, {"versioned_ensembl_gene_id":"ENSG00000229227.8","gene_symbol":"AL356056.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46597918,"end":46612154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254263.1","gene_symbol":"AC022973.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129890465,"end":129901758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163295.4","gene_symbol":"ALPI","gene_name":"alkaline phosphatase, intestinal [Source:HGNC Symbol;Acc:HGNC:437]","synonyms":null,"biotype":"protein_coding","ncbi_id":"248","summary":"There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The intestinal alkaline phosphatase gene encodes a digestive brush-border enzyme. This enzyme is a component of the gut mucosal defense system and is thought to function in the detoxification of lipopolysaccharide, and in the prevention of bacterial translocation in the gut. [provided by RefSeq, Dec 2014]","start":232456123,"end":232460032,"strand":1,"description":"alkaline phosphatase, intestinal [Source:HGNC Symbol;Acc:HGNC:437]"}, {"versioned_ensembl_gene_id":"ENSG00000104722.13","gene_symbol":"NEFM","gene_name":"neurofilament medium [Source:HGNC Symbol;Acc:HGNC:7734]","synonyms":"NFM,NF-M,NEF3","biotype":"protein_coding","ncbi_id":"4741","summary":"Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and functionally maintain neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the medium neurofilament protein. This protein is commonly used as a biomarker of neuronal damage. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]","start":24913012,"end":24919098,"strand":1,"description":"neurofilament medium [Source:HGNC Symbol;Acc:HGNC:7734]"}, {"versioned_ensembl_gene_id":"ENSG00000269799.1","gene_symbol":"AC008737.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16801426,"end":16801714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224643.5","gene_symbol":"AC064871.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":183083405,"end":183108519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231437.3","gene_symbol":"LINC01750","gene_name":"long intergenic non-protein coding RNA 1750 [Source:HGNC Symbol;Acc:HGNC:52538]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643355","summary":null,"start":111989770,"end":111998842,"strand":1,"description":"long intergenic non-protein coding RNA 1750 [Source:HGNC Symbol;Acc:HGNC:52538]"}, {"versioned_ensembl_gene_id":"ENSG00000167772.11","gene_symbol":"ANGPTL4","gene_name":"angiopoietin like 4 [Source:HGNC Symbol;Acc:HGNC:16039]","synonyms":"ARP4,pp1158,PGAR,NL2,HFARP,FIAF","biotype":"protein_coding","ncbi_id":"51129","summary":"This gene encodes a glycosylated, secreted protein containing a C-terminal fibrinogen domain. The encoded protein is induced by peroxisome proliferation activators and functions as a serum hormone that regulates glucose homeostasis, lipid metabolism, and insulin sensitivity. This protein can also act as an apoptosis survival factor for vascular endothelial cells and can prevent metastasis by inhibiting vascular growth and tumor cell invasion. The C-terminal domain may be proteolytically-cleaved from the full-length secreted protein. Decreased expression of this gene has been associated with type 2 diabetes. Alternative splicing results in multiple transcript variants. This gene was previously referred to as ANGPTL2 but has been renamed ANGPTL4. [provided by RefSeq, Sep 2013]","start":8363289,"end":8374373,"strand":1,"description":"angiopoietin like 4 [Source:HGNC Symbol;Acc:HGNC:16039]"}, {"versioned_ensembl_gene_id":"ENSG00000128713.13","gene_symbol":"HOXD11","gene_name":"homeobox D11 [Source:HGNC Symbol;Acc:HGNC:5134]","synonyms":"HOX4F,HOX4","biotype":"protein_coding","ncbi_id":"3237","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. The product of the mouse Hoxd11 gene plays a role in forelimb morphogenesis. [provided by RefSeq, Jul 2008]","start":176104216,"end":176109754,"strand":1,"description":"homeobox D11 [Source:HGNC Symbol;Acc:HGNC:5134]"}, {"versioned_ensembl_gene_id":"ENSG00000262214.1","gene_symbol":"KRTAP9-12P","gene_name":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287715","summary":null,"start":41212710,"end":41213241,"strand":1,"description":"keratin associated protein 9-12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48873]"}, {"versioned_ensembl_gene_id":"ENSG00000274243.5","gene_symbol":"GU182357.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54782617,"end":54797414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271320.1","gene_symbol":"AC091488.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157917712,"end":157918371,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270557.1","gene_symbol":"AC013731.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157877683,"end":157878565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227757.3","gene_symbol":"AP000282.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32913649,"end":33071104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133138.19","gene_symbol":"TBC1D8B","gene_name":"TBC1 domain family member 8B [Source:HGNC Symbol;Acc:HGNC:24715]","synonyms":"RP11-321G1.1,GRAMD8B,FLJ20298","biotype":"protein_coding","ncbi_id":"54885","summary":"This gene encodes a protein with a TBC (Tre-2/Bub2/CDC16) domain. Some mammalian proteins with this domain have been shown to function as Rab-GAPs by binding to specific Rab proteins and affecting their GTPase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":106802680,"end":106876145,"strand":1,"description":"TBC1 domain family member 8B [Source:HGNC Symbol;Acc:HGNC:24715]"}, {"versioned_ensembl_gene_id":"ENSG00000229223.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30094794,"end":30104272,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000269419.1","gene_symbol":"AC008737.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16712317,"end":16712434,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275040.1","gene_symbol":"AC009159.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79619469,"end":79620110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122482.20","gene_symbol":"ZNF644","gene_name":"zinc finger protein 644 [Source:HGNC Symbol;Acc:HGNC:29222]","synonyms":"MGC70410,MGC60165,KIAA1221,BM-005","biotype":"protein_coding","ncbi_id":"84146","summary":"The protein encoded by this gene is a zinc finger transcription factor that may play a role in eye development. Defects in this gene have been associated with high myopia. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":90915298,"end":91022272,"strand":-1,"description":"zinc finger protein 644 [Source:HGNC Symbol;Acc:HGNC:29222]"}, {"versioned_ensembl_gene_id":"ENSG00000277508.1","gene_symbol":"BSNDP3","gene_name":"barttin CLCNK type accessory beta subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51538]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481725","summary":null,"start":26071988,"end":26072351,"strand":-1,"description":"barttin CLCNK type accessory beta subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51538]"}, {"versioned_ensembl_gene_id":"ENSG00000233240.1","gene_symbol":"CR753309.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32504263,"end":32523409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229677.1","gene_symbol":"AC018644.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139049456,"end":139050006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188732.10","gene_symbol":"FAM221A","gene_name":"family with sequence similarity 221 member A [Source:HGNC Symbol;Acc:HGNC:27977]","synonyms":"MGC72075,FLJ45875,DKFZp686F0810,C7orf46","biotype":"protein_coding","ncbi_id":"340277","summary":null,"start":23680130,"end":23703249,"strand":1,"description":"family with sequence similarity 221 member A [Source:HGNC Symbol;Acc:HGNC:27977]"}, {"versioned_ensembl_gene_id":"ENSG00000244624.3","gene_symbol":"KRTAP20-1","gene_name":"keratin associated protein 20-1 [Source:HGNC Symbol;Acc:HGNC:18943]","synonyms":"KAP20.1","biotype":"protein_coding","ncbi_id":"337975","summary":null,"start":30616425,"end":30616699,"strand":1,"description":"keratin associated protein 20-1 [Source:HGNC Symbol;Acc:HGNC:18943]"}, {"versioned_ensembl_gene_id":"ENSG00000236556.1","gene_symbol":"AC025038.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59282147,"end":59282835,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109061.9","gene_symbol":"MYH1","gene_name":"myosin heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:7567]","synonyms":"MYHa,MGC133384,MYHSA1,MyHC-2X/D","biotype":"protein_coding","ncbi_id":"4619","summary":"Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. Myosin heavy chains are encoded by a multigene family. In mammals at least 10 different myosin heavy chain (MYH) isoforms have been described from striated, smooth, and nonmuscle cells. These isoforms show expression that is spatially and temporally regulated during development. [provided by RefSeq, Jul 2008]","start":10492307,"end":10518543,"strand":-1,"description":"myosin heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:7567]"}, {"versioned_ensembl_gene_id":"ENSG00000270976.1","gene_symbol":"AL596327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106780223,"end":106780435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280811.2","gene_symbol":"NDUFA6-AS1","gene_name":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100132273","summary":null,"start":42090933,"end":42137053,"strand":1,"description":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]"}, {"versioned_ensembl_gene_id":"ENSG00000134594.4","gene_symbol":"RAB33A","gene_name":"RAB33A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9773]","synonyms":"RabS10","biotype":"protein_coding","ncbi_id":"9363","summary":"The protein encoded by this gene belongs to the small GTPase superfamily, Rab family. It is GTP-binding protein and may be involved in vesicle transport. [provided by RefSeq, Jul 2008]","start":130171649,"end":130184870,"strand":1,"description":"RAB33A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9773]"}, {"versioned_ensembl_gene_id":"ENSG00000279428.1","gene_symbol":"AC087164.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18107334,"end":18110463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157856.10","gene_symbol":"DRC1","gene_name":"dynein regulatory complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24245]","synonyms":"MGC16372,FLJ32660,CILD21,CCDC164,C2orf39","biotype":"protein_coding","ncbi_id":"92749","summary":"This gene encodes a central component of the nexin-dynein complex (N-DRC), which regulates the assembly of ciliary dynein. Mutations in this gene can cause ciliary dyskinesia. [provided by RefSeq, Aug 2015]","start":26401916,"end":26456711,"strand":1,"description":"dynein regulatory complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24245]"}, {"versioned_ensembl_gene_id":"ENSG00000250636.1","gene_symbol":"AC019193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183028601,"end":183029720,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142677.3","gene_symbol":"IL22RA1","gene_name":"interleukin 22 receptor subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:13700]","synonyms":"IL22R,CRF2-9","biotype":"protein_coding","ncbi_id":"58985","summary":"The protein encoded by this gene belongs to the class II cytokine receptor family, and has been shown to be a receptor for interleukin 22 (IL22). IL22 receptor is a protein complex that consists of this protein and interleukin 10 receptor, beta (IL10BR/CRFB4), a subunit also shared by the receptor complex for interleukin 10 (IL10). This gene and interleukin 28 receptor, alpha (IL28RA) form a cytokine receptor gene cluster in the chromosomal region 1p36. [provided by RefSeq, Jul 2008]","start":24119771,"end":24143121,"strand":-1,"description":"interleukin 22 receptor subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:13700]"}, {"versioned_ensembl_gene_id":"ENSG00000251597.1","gene_symbol":"RPL37P25","gene_name":"ribosomal protein L37 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49020]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481666","summary":null,"start":54399439,"end":54400033,"strand":1,"description":"ribosomal protein L37 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49020]"}, {"versioned_ensembl_gene_id":"ENSG00000270171.1","gene_symbol":"AL359881.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7693124,"end":7694844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237728.2","gene_symbol":"Z97987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7382487,"end":7389754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229756.1","gene_symbol":"RPL31P20","gene_name":"ribosomal protein L31 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36303]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270986","summary":null,"start":24430748,"end":24431107,"strand":1,"description":"ribosomal protein L31 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36303]"}, {"versioned_ensembl_gene_id":"ENSG00000273759.1","gene_symbol":"AL117379.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62928621,"end":62929297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234383.1","gene_symbol":"CTBP2P8","gene_name":"C-terminal binding protein 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45200]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420253","summary":null,"start":68161761,"end":68163090,"strand":-1,"description":"C-terminal binding protein 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45200]"}, {"versioned_ensembl_gene_id":"ENSG00000217385.1","gene_symbol":"PSMC1P11","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39786]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442153","summary":null,"start":4702463,"end":4703779,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39786]"}, {"versioned_ensembl_gene_id":"ENSG00000278826.1","gene_symbol":"AC009892.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54616083,"end":54616589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256609.1","gene_symbol":"AC084880.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119182048,"end":119183259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267199.1","gene_symbol":"AP001029.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12438890,"end":12448205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268058.1","gene_symbol":"BNIP3P40","gene_name":"BCL2 interacting protein 3 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:49720]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421702","summary":null,"start":24098425,"end":24098980,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:49720]"}, {"versioned_ensembl_gene_id":"ENSG00000279425.1","gene_symbol":"AC092279.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24078481,"end":24080669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234286.1","gene_symbol":"AC006026.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23680195,"end":23680786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273692.1","gene_symbol":"AL050303.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13704853,"end":13705518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140750.16","gene_symbol":"ARHGAP17","gene_name":"Rho GTPase activating protein 17 [Source:HGNC Symbol;Acc:HGNC:18239]","synonyms":"WBP15,RICH1,NADRIN,FLJ13219,FLJ10308","biotype":"protein_coding","ncbi_id":"55114","summary":"RICH1 is a GTPase-activating protein (GAP). GAPs stimulate the intrinsic GTP hydrolysis of small G proteins, such as RHOA (MIM 165390), RAC1 (MIM 602048), and CDC42 (MIM 116952).[supplied by OMIM, Apr 2004]","start":24919385,"end":25015666,"strand":-1,"description":"Rho GTPase activating protein 17 [Source:HGNC Symbol;Acc:HGNC:18239]"}, {"versioned_ensembl_gene_id":"ENSG00000138185.19","gene_symbol":"ENTPD1","gene_name":"ectonucleoside triphosphate diphosphohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3363]","synonyms":"SPG64,NTPDase-1,CD39,ATPDase","biotype":"protein_coding","ncbi_id":"953","summary":"The protein encoded by this gene is a plasma membrane protein that hydrolyzes extracellular ATP and ADP to AMP. Inhibition of this protein's activity may confer anticancer benefits. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":95711779,"end":95869695,"strand":1,"description":"ectonucleoside triphosphate diphosphohydrolase 1 [Source:HGNC Symbol;Acc:HGNC:3363]"}, {"versioned_ensembl_gene_id":"ENSG00000280360.1","gene_symbol":"AC092159.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":687799,"end":688348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138496.16","gene_symbol":"PARP9","gene_name":"poly(ADP-ribose) polymerase family member 9 [Source:HGNC Symbol;Acc:HGNC:24118]","synonyms":"BAL1,BAL","biotype":"protein_coding","ncbi_id":"83666","summary":null,"start":122527924,"end":122564577,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 9 [Source:HGNC Symbol;Acc:HGNC:24118]"}, {"versioned_ensembl_gene_id":"ENSG00000273011.1","gene_symbol":"AC092681.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149890739,"end":149891416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114739.13","gene_symbol":"ACVR2B","gene_name":"activin A receptor type 2B [Source:HGNC Symbol;Acc:HGNC:174]","synonyms":"ActR-IIB","biotype":"protein_coding","ncbi_id":"93","summary":"Activins are dimeric growth and differentiation factors which belong to the transforming growth factor-beta (TGF-beta) superfamily of structurally related signaling proteins. Activins signal through a heteromeric complex of receptor serine kinases which include at least two type I (I and IB) and two type II (II and IIB) receptors. These receptors are all transmembrane proteins, composed of a ligand-binding extracellular domain with cysteine-rich region, a transmembrane domain, and a cytoplasmic domain with predicted serine/threonine specificity. Type I receptors are essential for signaling; and type II receptors are required for binding ligands and for expression of type I receptors. Type I and II receptors form a stable complex after ligand binding, resulting in phosphorylation of type I receptors by type II receptors. Type II receptors are considered to be constitutively active kinases. This gene encodes activin A type IIB receptor, which displays a 3- to 4-fold higher affinity for the ligand than activin A type II receptor. [provided by RefSeq, Jul 2008]","start":38453851,"end":38493142,"strand":1,"description":"activin A receptor type 2B [Source:HGNC Symbol;Acc:HGNC:174]"}, {"versioned_ensembl_gene_id":"ENSG00000237480.2","gene_symbol":"AL355306.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105956694,"end":106124564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218125.1","gene_symbol":"AP000567.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30526546,"end":30526701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235312.1","gene_symbol":"KRTAP19-10P","gene_name":"keratin associated protein 19-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:18951]","synonyms":"KRTAP19P2,KAP19B","biotype":"unprocessed_pseudogene","ncbi_id":"337983","summary":null,"start":30514613,"end":30514799,"strand":-1,"description":"keratin associated protein 19-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:18951]"}, {"versioned_ensembl_gene_id":"ENSG00000256171.1","gene_symbol":"GCSHP4","gene_name":"glycine cleavage system protein H pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287495","summary":null,"start":8141168,"end":8142697,"strand":-1,"description":"glycine cleavage system protein H pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43930]"}, {"versioned_ensembl_gene_id":"ENSG00000237841.1","gene_symbol":"KRTAP19-9P","gene_name":"keratin associated protein 19-9, pseudogene [Source:HGNC Symbol;Acc:HGNC:18950]","synonyms":"KRTAP19P1,KAP19A","biotype":"unprocessed_pseudogene","ncbi_id":"337982","summary":null,"start":30510307,"end":30510497,"strand":-1,"description":"keratin associated protein 19-9, pseudogene [Source:HGNC Symbol;Acc:HGNC:18950]"}, {"versioned_ensembl_gene_id":"ENSG00000279773.1","gene_symbol":"AL050303.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":13679300,"end":13681138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236670.1","gene_symbol":"KRT18P5","gene_name":"keratin 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19259]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728300","summary":null,"start":20482815,"end":20484105,"strand":-1,"description":"keratin 18 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19259]"}, {"versioned_ensembl_gene_id":"ENSG00000224205.1","gene_symbol":"AC253536.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23987320,"end":23991421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282606.1","gene_symbol":"AC068473.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79644682,"end":79685499,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272338.2","gene_symbol":"AC067838.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33360839,"end":33361415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231569.1","gene_symbol":"AL355334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87408044,"end":87408258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250003.2","gene_symbol":"LINC02107","gene_name":"long intergenic non-protein coding RNA 2107 [Source:HGNC Symbol;Acc:HGNC:52962]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374731","summary":null,"start":38025697,"end":38183932,"strand":1,"description":"long intergenic non-protein coding RNA 2107 [Source:HGNC Symbol;Acc:HGNC:52962]"}, {"versioned_ensembl_gene_id":"ENSG00000238139.2","gene_symbol":"AL590559.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67561073,"end":67561446,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275300.4","gene_symbol":"MCCC2","gene_name":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]","synonyms":"MCCB","biotype":"protein_coding","ncbi_id":"64087","summary":"This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018]","start":70802600,"end":70819771,"strand":1,"description":"methylcrotonoyl-CoA carboxylase 2 [Source:HGNC Symbol;Acc:HGNC:6937]"}, {"versioned_ensembl_gene_id":"ENSG00000229741.7","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"BTN7,HSBLMHC1,BTL-II,HSBLMHC1,BTL-II,BTN7","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32369461,"end":32382615,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000257265.1","gene_symbol":"AC123905.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71007773,"end":71032083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232918.2","gene_symbol":"AC118469.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94406395,"end":94406882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259359.1","gene_symbol":"AC012409.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96171581,"end":96174339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178081.12","gene_symbol":"ULK4P3","gene_name":"ULK4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:15777]","synonyms":"FAM7A3,D-X","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"89837","summary":null,"start":30103720,"end":30131757,"strand":1,"description":"ULK4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:15777]"}, {"versioned_ensembl_gene_id":"ENSG00000278381.1","gene_symbol":"AL050303.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13654073,"end":13654356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112977.15","gene_symbol":"DAP","gene_name":"death associated protein [Source:HGNC Symbol;Acc:HGNC:2672]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1611","summary":"This gene encodes a basic, proline-rich, 15-kD protein. The protein acts as a positive mediator of programmed cell death that is induced by interferon-gamma. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":10679230,"end":10761272,"strand":-1,"description":"death associated protein [Source:HGNC Symbol;Acc:HGNC:2672]"}, {"versioned_ensembl_gene_id":"ENSG00000214124.3","gene_symbol":"SNRPEP9","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:43574]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874416","summary":null,"start":24513450,"end":24513687,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:43574]"}, {"versioned_ensembl_gene_id":"ENSG00000166068.12","gene_symbol":"SPRED1","gene_name":"sprouty related EVH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20249]","synonyms":"PPP1R147,FLJ33903","biotype":"protein_coding","ncbi_id":"161742","summary":"The protein encoded by this gene is a member of the Sprouty family of proteins and is phosphorylated by tyrosine kinase in response to several growth factors. The encoded protein can act as a homodimer or as a heterodimer with SPRED2 to regulate activation of the MAP kinase cascade. Defects in this gene are a cause of neurofibromatosis type 1-like syndrome (NFLS). [provided by RefSeq, Jul 2008]","start":38252326,"end":38357249,"strand":1,"description":"sprouty related EVH1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20249]"}, {"versioned_ensembl_gene_id":"ENSG00000241439.1","gene_symbol":"AC092903.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125958556,"end":125958817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217060.1","gene_symbol":"AL135903.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85286076,"end":85290849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280291.1","gene_symbol":"AC016251.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":96294935,"end":96298023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231381.2","gene_symbol":"RNF2P1","gene_name":"ring finger protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33987]","synonyms":"RNF2P","biotype":"processed_pseudogene","ncbi_id":"100132467","summary":null,"start":6668999,"end":6670008,"strand":-1,"description":"ring finger protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33987]"}, {"versioned_ensembl_gene_id":"ENSG00000186638.16","gene_symbol":"KIF24","gene_name":"kinesin family member 24 [Source:HGNC Symbol;Acc:HGNC:19916]","synonyms":"FLJ43884,FLJ10933,C9orf48,bA571F15.4","biotype":"protein_coding","ncbi_id":"347240","summary":"This gene encodes a member of the kinesin superfamily of microtubule-based motor proteins which are involved in the intracellular transport of membranous organelles, protein complexes, and mRNAs. They also play critical roles in mitosis, morphogenesis, and signal transduction. The encoded protein contains an N-terminal sterile alpha motif (SAM) domain and an ATP-binding kinesin motor domain. It binds centriolar coiled coil protein 110 and centrosomal protein 97 and localizes to the mother centriole to regulate ciliogenesis by controlling microtubule polymerization. [provided by RefSeq, Mar 2017]","start":34252381,"end":34311371,"strand":-1,"description":"kinesin family member 24 [Source:HGNC Symbol;Acc:HGNC:19916]"}, {"versioned_ensembl_gene_id":"ENSG00000273294.1","gene_symbol":"C1QTNF3-AMACR","gene_name":"C1QTNF3-AMACR readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534612","summary":"This locus represents naturally occurring read-through transcription between the neighboring C1q and tumor necrosis factor related protein 3 (C1QTNF3) and alpha-methylacyl-CoA racemase (AMACR) genes on chromosome 5. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus not likely to produce a protein product. [provided by RefSeq, Mar 2011]","start":33987174,"end":34124528,"strand":-1,"description":"C1QTNF3-AMACR readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49198]"}, {"versioned_ensembl_gene_id":"ENSG00000250767.1","gene_symbol":"AC139783.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33997044,"end":33997724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283654.1","gene_symbol":"AL117258.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23099065,"end":23104992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204610.12","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"RNF93,ZNFB7,ZNF178","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30163206,"end":30172696,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000255364.1","gene_symbol":"SMILR","gene_name":"smooth muscle induced lncRNA, enhancer of proliferation [Source:HGNC Symbol;Acc:HGNC:51825]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105375734","summary":null,"start":122414332,"end":122428551,"strand":-1,"description":"smooth muscle induced lncRNA, enhancer of proliferation [Source:HGNC Symbol;Acc:HGNC:51825]"}, {"versioned_ensembl_gene_id":"ENSG00000253814.1","gene_symbol":"MRPS36P3","gene_name":"mitochondrial ribosomal protein S36 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29773]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347704","summary":null,"start":122091480,"end":122091609,"strand":1,"description":"mitochondrial ribosomal protein S36 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29773]"}, {"versioned_ensembl_gene_id":"ENSG00000184351.7","gene_symbol":"KRTAP19-1","gene_name":"keratin associated protein 19-1 [Source:HGNC Symbol;Acc:HGNC:18936]","synonyms":"KAP19.1","biotype":"protein_coding","ncbi_id":"337882","summary":null,"start":30479699,"end":30480344,"strand":-1,"description":"keratin associated protein 19-1 [Source:HGNC Symbol;Acc:HGNC:18936]"}, {"versioned_ensembl_gene_id":"ENSG00000282376.1","gene_symbol":"AL161631.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101125436,"end":101125921,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165006.13","gene_symbol":"UBAP1","gene_name":"ubiquitin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:12461]","synonyms":"UBAP","biotype":"protein_coding","ncbi_id":"51271","summary":"This gene is a member of the UBA domain family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin binding domain consisting of a compact three helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC). Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":34179005,"end":34252523,"strand":1,"description":"ubiquitin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:12461]"}, {"versioned_ensembl_gene_id":"ENSG00000221890.3","gene_symbol":"NPTXR","gene_name":"neuronal pentraxin receptor [Source:HGNC Symbol;Acc:HGNC:7954]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23467","summary":"This gene encodes a protein similar to the rat neuronal pentraxin receptor. The rat pentraxin receptor is an integral membrane protein that is thought to mediate neuronal uptake of the snake venom toxin, taipoxin, and its transport into the synapses. Studies in rat indicate that translation of this mRNA initiates at a non-AUG (CUG) codon. This may also be true for mouse and human, based on strong sequence conservation amongst these species. [provided by RefSeq, Jul 2008]","start":38818452,"end":38843982,"strand":-1,"description":"neuronal pentraxin receptor [Source:HGNC Symbol;Acc:HGNC:7954]"}, {"versioned_ensembl_gene_id":"ENSG00000234272.1","gene_symbol":"RPL30P2","gene_name":"ribosomal protein L30 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270976","summary":null,"start":152131555,"end":152131845,"strand":1,"description":"ribosomal protein L30 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35642]"}, {"versioned_ensembl_gene_id":"ENSG00000111669.14","gene_symbol":"TPI1","gene_name":"triosephosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:12009]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7167","summary":"This gene encodes an enzyme, consisting of two identical proteins, which catalyzes the isomerization of glyceraldehydes 3-phosphate (G3P) and dihydroxy-acetone phosphate (DHAP) in glycolysis and gluconeogenesis. Mutations in this gene are associated with triosephosphate isomerase deficiency. Pseudogenes have been identified on chromosomes 1, 4, 6 and 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":6867119,"end":6870948,"strand":1,"description":"triosephosphate isomerase 1 [Source:HGNC Symbol;Acc:HGNC:12009]"}, {"versioned_ensembl_gene_id":"ENSG00000240566.1","gene_symbol":"AC010153.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24650808,"end":24651534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279865.1","gene_symbol":"AC006511.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8080381,"end":8082163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224299.1","gene_symbol":"MTATP6P16","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52061]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075158","summary":null,"start":201550524,"end":201551049,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:52061]"}, {"versioned_ensembl_gene_id":"ENSG00000250078.1","gene_symbol":"AC019133.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58562165,"end":58565122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203858.3","gene_symbol":"HSD3BP2","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5220]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440606","summary":null,"start":119439001,"end":119446086,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5220]"}, {"versioned_ensembl_gene_id":"ENSG00000132801.6","gene_symbol":"ZSWIM3","gene_name":"zinc finger SWIM-type containing 3 [Source:HGNC Symbol;Acc:HGNC:16157]","synonyms":"PPP1R174,dJ337O18.7,C20orf164","biotype":"protein_coding","ncbi_id":"140831","summary":null,"start":45857617,"end":45879122,"strand":1,"description":"zinc finger SWIM-type containing 3 [Source:HGNC Symbol;Acc:HGNC:16157]"}, {"versioned_ensembl_gene_id":"ENSG00000262089.1","gene_symbol":"AC040977.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6994642,"end":6995189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242229.1","gene_symbol":"RPS3AP14","gene_name":"ribosomal protein S3a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35715]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729150","summary":null,"start":125795106,"end":125795885,"strand":1,"description":"ribosomal protein S3a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35715]"}, {"versioned_ensembl_gene_id":"ENSG00000284660.1","gene_symbol":"AC092902.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125766601,"end":125766818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239804.1","gene_symbol":"AC092902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125787888,"end":125788146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123612.15","gene_symbol":"ACVR1C","gene_name":"activin A receptor type 1C [Source:HGNC Symbol;Acc:HGNC:18123]","synonyms":"ALK7,ACVRLK7","biotype":"protein_coding","ncbi_id":"130399","summary":"ACVR1C is a type I receptor for the TGFB (see MIM 190180) family of signaling molecules. Upon ligand binding, type I receptors phosphorylate cytoplasmic SMAD transcription factors, which then translocate to the nucleus and interact directly with DNA or in complex with other transcription factors (Bondestam et al., 2001 [PubMed 12063393]).[supplied by OMIM, Mar 2008]","start":157526767,"end":157629005,"strand":-1,"description":"activin A receptor type 1C [Source:HGNC Symbol;Acc:HGNC:18123]"}, {"versioned_ensembl_gene_id":"ENSG00000257115.1","gene_symbol":"OR11H12","gene_name":"olfactory receptor family 11 subfamily H member 12 [Source:HGNC Symbol;Acc:HGNC:30738]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440153","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":18601045,"end":18602129,"strand":1,"description":"olfactory receptor family 11 subfamily H member 12 [Source:HGNC Symbol;Acc:HGNC:30738]"}, {"versioned_ensembl_gene_id":"ENSG00000167969.12","gene_symbol":"ECI1","gene_name":"enoyl-CoA delta isomerase 1 [Source:HGNC Symbol;Acc:HGNC:2703]","synonyms":"DCI","biotype":"protein_coding","ncbi_id":"1632","summary":"This gene encodes a member of the hydratase/isomerase superfamily. The protein encoded is a key mitochondrial enzyme involved in beta-oxidation of unsaturated fatty acids. It catalyzes the transformation of 3-cis and 3-trans-enoyl-CoA esters arising during the stepwise degradation of cis-, mono-, and polyunsaturated fatty acids to the 2-trans-enoyl-CoA intermediates. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2010]","start":2239395,"end":2252300,"strand":-1,"description":"enoyl-CoA delta isomerase 1 [Source:HGNC Symbol;Acc:HGNC:2703]"}, {"versioned_ensembl_gene_id":"ENSG00000251518.1","gene_symbol":"LINC02110","gene_name":"long intergenic non-protein coding RNA 2110 [Source:HGNC Symbol;Acc:HGNC:52965]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374729","summary":null,"start":37948491,"end":37951055,"strand":1,"description":"long intergenic non-protein coding RNA 2110 [Source:HGNC Symbol;Acc:HGNC:52965]"}, {"versioned_ensembl_gene_id":"ENSG00000228146.7","gene_symbol":"CASP16P","gene_name":"caspase 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:27290]","synonyms":"CASP16","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"197350","summary":null,"start":3144219,"end":3149963,"strand":1,"description":"caspase 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:27290]"}, {"versioned_ensembl_gene_id":"ENSG00000111252.10","gene_symbol":"SH2B3","gene_name":"SH2B adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:29605]","synonyms":"LNK,IDDM20","biotype":"protein_coding","ncbi_id":"10019","summary":"This gene encodes a member of the SH2B adaptor family of proteins, which are involved in a range of signaling activities by growth factor and cytokine receptors. The encoded protein is a key negative regulator of cytokine signaling and plays a critical role in hematopoiesis. Mutations in this gene have been associated with susceptibility to celiac disease type 13 and susceptibility to insulin-dependent diabetes mellitus. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":111405948,"end":111451623,"strand":1,"description":"SH2B adaptor protein 3 [Source:HGNC Symbol;Acc:HGNC:29605]"}, {"versioned_ensembl_gene_id":"ENSG00000136240.9","gene_symbol":"KDELR2","gene_name":"KDEL endoplasmic reticulum protein retention receptor 2 [Source:HGNC Symbol;Acc:HGNC:6305]","synonyms":"ERD2.2,ELP-1","biotype":"protein_coding","ncbi_id":"11014","summary":"Retention of resident soluble proteins in the lumen of the endoplasmic reticulum (ER) is achieved in both yeast and animal cells by their continual retrieval from the cis-Golgi, or a pre-Golgi compartment. Sorting of these proteins is dependent on a C-terminal tetrapeptide signal, usually lys-asp-glu-leu (KDEL) in animal cells, and his-asp-glu-leu (HDEL) in S. cerevisiae. This process is mediated by a receptor that recognizes, and binds the tetrapeptide-containing protein, and returns it to the ER. In yeast, the sorting receptor encoded by a single gene, ERD2, is a seven-transmembrane protein. Unlike yeast, several human homologs of the ERD2 gene, constituting the KDEL receptor gene family, have been described. KDELR2 was the second member of the family to be identified, and it encodes a protein which is 83% identical to the KDELR1 gene product. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":6445953,"end":6484242,"strand":-1,"description":"KDEL endoplasmic reticulum protein retention receptor 2 [Source:HGNC Symbol;Acc:HGNC:6305]"}, {"versioned_ensembl_gene_id":"ENSG00000103342.12","gene_symbol":"GSPT1","gene_name":"G1 to S phase transition 1 [Source:HGNC Symbol;Acc:HGNC:4621]","synonyms":"GST1,ETF3A,eRF3a","biotype":"protein_coding","ncbi_id":"2935","summary":null,"start":11868128,"end":11916082,"strand":-1,"description":"G1 to S phase transition 1 [Source:HGNC Symbol;Acc:HGNC:4621]"}, {"versioned_ensembl_gene_id":"ENSG00000250032.1","gene_symbol":"AC008869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37939365,"end":37947955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223746.1","gene_symbol":"ELOCP30","gene_name":"elongin C pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49171]","synonyms":"TCEB1P30","biotype":"processed_pseudogene","ncbi_id":"106481670","summary":null,"start":43741437,"end":43742350,"strand":-1,"description":"elongin C pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49171]"}, {"versioned_ensembl_gene_id":"ENSG00000234973.5","gene_symbol":"AL355989.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43777562,"end":43778825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215110.7","gene_symbol":"UGT2B25P","gene_name":"UDP glucuronosyltransferase family 2 member B25, pseudogene [Source:HGNC Symbol;Acc:HGNC:12549]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54571","summary":null,"start":69389492,"end":69402081,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B25, pseudogene [Source:HGNC Symbol;Acc:HGNC:12549]"}, {"versioned_ensembl_gene_id":"ENSG00000183055.5","gene_symbol":"FAM133CP","gene_name":"family with sequence similarity 133 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44190]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728640","summary":null,"start":58715554,"end":58716257,"strand":1,"description":"family with sequence similarity 133 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44190]"}, {"versioned_ensembl_gene_id":"ENSG00000213742.6","gene_symbol":"ZNF337-AS1","gene_name":"ZNF337 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40759]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724826","summary":null,"start":25624045,"end":25678074,"strand":1,"description":"ZNF337 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40759]"}, {"versioned_ensembl_gene_id":"ENSG00000174442.11","gene_symbol":"ZWILCH","gene_name":"zwilch kinetochore protein [Source:HGNC Symbol;Acc:HGNC:25468]","synonyms":"KNTC1AP,FLJ10036","biotype":"protein_coding","ncbi_id":"55055","summary":null,"start":66504959,"end":66550128,"strand":1,"description":"zwilch kinetochore protein [Source:HGNC Symbol;Acc:HGNC:25468]"}, {"versioned_ensembl_gene_id":"ENSG00000224162.1","gene_symbol":"UQCRHP3","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38046]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131995","summary":null,"start":43732334,"end":43732584,"strand":1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38046]"}, {"versioned_ensembl_gene_id":"ENSG00000247095.2","gene_symbol":"MIR210HG","gene_name":"MIR210 host gene [Source:HGNC Symbol;Acc:HGNC:39524]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506211","summary":null,"start":565660,"end":568457,"strand":-1,"description":"MIR210 host gene [Source:HGNC Symbol;Acc:HGNC:39524]"}, {"versioned_ensembl_gene_id":"ENSG00000102572.14","gene_symbol":"STK24","gene_name":"serine/threonine kinase 24 [Source:HGNC Symbol;Acc:HGNC:11403]","synonyms":"STK3,STE20,MST3B,MST3,MST-3","biotype":"protein_coding","ncbi_id":"8428","summary":"This gene encodes a serine/threonine protein kinase that functions upstream of mitogen-activated protein kinase (MAPK) signaling. The encoded protein is cleaved into two chains by caspases; the N-terminal fragment (MST3/N) translocates to the nucleus and promotes programmed cells death. There is a pseudogene for this gene on chromosome X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":98445185,"end":98577940,"strand":-1,"description":"serine/threonine kinase 24 [Source:HGNC Symbol;Acc:HGNC:11403]"}, {"versioned_ensembl_gene_id":"ENSG00000139880.19","gene_symbol":"CDH24","gene_name":"cadherin 24 [Source:HGNC Symbol;Acc:HGNC:14265]","synonyms":"CDH11L","biotype":"protein_coding","ncbi_id":"64403","summary":null,"start":23047062,"end":23057538,"strand":-1,"description":"cadherin 24 [Source:HGNC Symbol;Acc:HGNC:14265]"}, {"versioned_ensembl_gene_id":"ENSG00000272256.1","gene_symbol":"AC044849.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30082758,"end":30083467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234458.4","gene_symbol":"AF186996.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125703349,"end":125704312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231550.1","gene_symbol":"PTCHD3P2","gene_name":"patched domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533664","summary":null,"start":169767185,"end":169768799,"strand":-1,"description":"patched domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44946]"}, {"versioned_ensembl_gene_id":"ENSG00000231005.1","gene_symbol":"RPL39P39","gene_name":"ribosomal protein L39 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36514]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271530","summary":null,"start":57328546,"end":57328696,"strand":1,"description":"ribosomal protein L39 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36514]"}, {"versioned_ensembl_gene_id":"ENSG00000101003.9","gene_symbol":"GINS1","gene_name":"GINS complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28980]","synonyms":"PSF1,KIAA0186","biotype":"protein_coding","ncbi_id":"9837","summary":"The yeast heterotetrameric GINS complex is made up of Sld5 (GINS4; MIM 610611), Psf1, Psf2 (GINS2; MIM 610609), and Psf3 (GINS3; MIM 610610). The formation of the GINS complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]).[supplied by OMIM, Mar 2008]","start":25407727,"end":25452628,"strand":1,"description":"GINS complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:28980]"}, {"versioned_ensembl_gene_id":"ENSG00000105829.11","gene_symbol":"BET1","gene_name":"Bet1 golgi vesicular membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:14562]","synonyms":"hbet1","biotype":"protein_coding","ncbi_id":"10282","summary":"This gene encodes a golgi-associated membrane protein that participates in vesicular transport from the endoplasmic reticulum (ER) to the Golgi complex. The encoded protein functions as a soluble N-ethylaleimide-sensitive factor attachment protein receptor and may be involved in the docking of ER-derived vesicles with the cis-Golgi membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":93962762,"end":94004382,"strand":-1,"description":"Bet1 golgi vesicular membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:14562]"}, {"versioned_ensembl_gene_id":"ENSG00000203737.3","gene_symbol":"GPR52","gene_name":"G protein-coupled receptor 52 [Source:HGNC Symbol;Acc:HGNC:4508]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9293","summary":"Members of the G protein-coupled receptor (GPR) family play important roles in signal transduction from the external environment to the inside of the cell.[supplied by OMIM, Jul 2002]","start":174448111,"end":174449198,"strand":1,"description":"G protein-coupled receptor 52 [Source:HGNC Symbol;Acc:HGNC:4508]"}, {"versioned_ensembl_gene_id":"ENSG00000263236.2","gene_symbol":"KRTAP4-12","gene_name":"keratin associated protein 4-12 [Source:HGNC Symbol;Acc:HGNC:16776]","synonyms":"KAP4.12","biotype":"protein_coding","ncbi_id":"83755","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41123559,"end":41124635,"strand":-1,"description":"keratin associated protein 4-12 [Source:HGNC Symbol;Acc:HGNC:16776]"}, {"versioned_ensembl_gene_id":"ENSG00000134153.9","gene_symbol":"EMC7","gene_name":"ER membrane protein complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:24301]","synonyms":"C15orf24,C11orf3","biotype":"protein_coding","ncbi_id":"56851","summary":null,"start":34084017,"end":34101948,"strand":-1,"description":"ER membrane protein complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:24301]"}, {"versioned_ensembl_gene_id":"ENSG00000171490.12","gene_symbol":"RSL1D1","gene_name":"ribosomal L1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24534]","synonyms":"UTP30,PBK1,L12,DKFZP564M182,CSIG","biotype":"protein_coding","ncbi_id":"26156","summary":null,"start":11833850,"end":11851585,"strand":-1,"description":"ribosomal L1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24534]"}, {"versioned_ensembl_gene_id":"ENSG00000271949.1","gene_symbol":"AC093423.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":89633140,"end":89933250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226394.2","gene_symbol":"AC093423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89661212,"end":89661353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211662.2","gene_symbol":"IGLV3-21","gene_name":"immunoglobulin lambda variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5905]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28796","summary":null,"start":22711689,"end":22713203,"strand":1,"description":"immunoglobulin lambda variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5905]"}, {"versioned_ensembl_gene_id":"ENSG00000177504.10","gene_symbol":"VCX2","gene_name":"variable charge, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:18158]","synonyms":"VCX-2r","biotype":"protein_coding","ncbi_id":"51480","summary":"This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes that are expressed exclusively in male germ cells. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. This gene contains two copies of a 30 nt tandem repeat. Deletion of a nearby member of this family was implicated in cognitive disability. [provided by RefSeq, Feb 2015]","start":8169944,"end":8171267,"strand":-1,"description":"variable charge, X-linked 2 [Source:HGNC Symbol;Acc:HGNC:18158]"}, {"versioned_ensembl_gene_id":"ENSG00000222028.3","gene_symbol":"PSMB11","gene_name":"proteasome subunit beta 11 [Source:HGNC Symbol;Acc:HGNC:31963]","synonyms":"beta5t","biotype":"protein_coding","ncbi_id":"122706","summary":"Proteasomes generate peptides that are presented by major histocompatibility complex (MHC) I molecules to other cells of the immune system. Proteolysis is conducted by 20S proteasomes, complexes of 28 subunits arranged as a cylinder in 4 heteroheptameric rings: alpha-1 to -7, beta-1 to -7, beta-1 to -7, and alpha-1 to -7. The catalytic subunits are beta-1 (PSMB6; MIM 600307), beta-2 (PSMB7; MIM 604030), and beta-5 (PSMB5; MIM 600306). Three additional subunits, beta-1i (PSMB9; MIM 177045), beta-2i (PSMB10; MIM 176847), and beta-5i (PSMB8; MIM 177046), are induced by gamma-interferon (IFNG; MIM 147570) and are preferentially incorporated into proteasomes to make immunoproteasomes. PSMB11, or beta-5t, is a catalytic subunit expressed exclusively in cortical thymic epithelial cells (Murata et al., 2007 [PubMed 17540904]).[supplied by OMIM, Mar 2008]","start":23042167,"end":23044276,"strand":1,"description":"proteasome subunit beta 11 [Source:HGNC Symbol;Acc:HGNC:31963]"}, {"versioned_ensembl_gene_id":"ENSG00000231613.1","gene_symbol":"AC099568.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89788914,"end":89790492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164659.14","gene_symbol":"KIAA1324L","gene_name":"KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]","synonyms":"FLJ31340,EIG121L","biotype":"protein_coding","ncbi_id":"222223","summary":null,"start":86876906,"end":87059699,"strand":-1,"description":"KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]"}, {"versioned_ensembl_gene_id":"ENSG00000277144.1","gene_symbol":"AC092757.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59115547,"end":59116089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275960.4","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"CD158B1,nkat6,CD158k,cl-43","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54476158,"end":54520914,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000283133.1","gene_symbol":"AC021753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41157175,"end":41157342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119977.20","gene_symbol":"TCTN3","gene_name":"tectonic family member 3 [Source:HGNC Symbol;Acc:HGNC:24519]","synonyms":"TECT3,JBTS18,DKFZP564D116,C10orf61","biotype":"protein_coding","ncbi_id":"26123","summary":"This gene encodes a member of the tectonic gene family which functions in Hedgehog signal transduction and development of the neural tube. Mutations in this gene have been associated with Orofaciodigital Syndrome IV and Joubert Syndrom 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012]","start":95663396,"end":95694143,"strand":-1,"description":"tectonic family member 3 [Source:HGNC Symbol;Acc:HGNC:24519]"}, {"versioned_ensembl_gene_id":"ENSG00000261862.2","gene_symbol":"KRTAP1-5","gene_name":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]","synonyms":"KAP1.5","biotype":"protein_coding","ncbi_id":"83895","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41026153,"end":41027329,"strand":-1,"description":"keratin associated protein 1-5 [Source:HGNC Symbol;Acc:HGNC:16777]"}, {"versioned_ensembl_gene_id":"ENSG00000268078.1","gene_symbol":"AC135012.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86158206,"end":86158798,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261177.1","gene_symbol":"AC135012.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86081409,"end":86089526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280147.1","gene_symbol":"AC084026.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29587001,"end":29588426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186184.16","gene_symbol":"POLR1D","gene_name":"RNA polymerase I subunit D [Source:HGNC Symbol;Acc:HGNC:20422]","synonyms":"RPO1-3,RPAC2,RPA9,RPA16,MGC9850","biotype":"protein_coding","ncbi_id":"51082","summary":"The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]","start":27620742,"end":27744237,"strand":1,"description":"RNA polymerase I subunit D [Source:HGNC Symbol;Acc:HGNC:20422]"}, {"versioned_ensembl_gene_id":"ENSG00000273552.1","gene_symbol":"AL136439.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27667540,"end":27680566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254131.1","gene_symbol":"AC093367.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42484600,"end":42485019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274511.5","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54476178,"end":54488196,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000227240.1","gene_symbol":"AL356272.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":194149473,"end":194198694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255058.1","gene_symbol":"PDCL2P2","gene_name":"phosducin-like 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50341]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480295","summary":null,"start":65160194,"end":65160382,"strand":-1,"description":"phosducin-like 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50341]"}, {"versioned_ensembl_gene_id":"ENSG00000279604.1","gene_symbol":"AC092723.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86035627,"end":86036419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282680.1","gene_symbol":"AP005902.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39705172,"end":39705484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237213.2","gene_symbol":"RPL23AP22","gene_name":"ribosomal protein L23a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35505]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271291","summary":null,"start":193756815,"end":193757267,"strand":-1,"description":"ribosomal protein L23a pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35505]"}, {"versioned_ensembl_gene_id":"ENSG00000259750.1","gene_symbol":"AC092868.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59401221,"end":59402004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176371.13","gene_symbol":"ZSCAN2","gene_name":"zinc finger and SCAN domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20994]","synonyms":"ZNF854,ZFP29,FLJ20595","biotype":"protein_coding","ncbi_id":"54993","summary":"The protein encoded by this gene contains several copies of zinc finger motif, which is commonly found in transcriptional regulatory proteins. Studies in mice show that this gene is expressed during embryonic development, and specifically in the testis in adult mice, suggesting that it may play a role in regulating genes in germ cells. Alternative splicing of this gene results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":84600986,"end":84627796,"strand":1,"description":"zinc finger and SCAN domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20994]"}, {"versioned_ensembl_gene_id":"ENSG00000267924.1","gene_symbol":"AC139769.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23817599,"end":23874701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227811.2","gene_symbol":"FAM212B-AS1","gene_name":"FAM212B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49446]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506343","summary":null,"start":111739841,"end":111747798,"strand":1,"description":"FAM212B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49446]"}, {"versioned_ensembl_gene_id":"ENSG00000214846.4","gene_symbol":"AC114744.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15730962,"end":15731627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232077.1","gene_symbol":"LINC01031","gene_name":"long intergenic non-protein coding RNA 1031 [Source:HGNC Symbol;Acc:HGNC:49017]","synonyms":"TCONS_00000361","biotype":"lincRNA","ncbi_id":"101929184","summary":null,"start":193304745,"end":193365953,"strand":1,"description":"long intergenic non-protein coding RNA 1031 [Source:HGNC Symbol;Acc:HGNC:49017]"}, {"versioned_ensembl_gene_id":"ENSG00000039987.6","gene_symbol":"BEST2","gene_name":"bestrophin 2 [Source:HGNC Symbol;Acc:HGNC:17107]","synonyms":"VMD2L1,FLJ20132","biotype":"protein_coding","ncbi_id":"54831","summary":"This gene is a member of the bestrophin gene family of anion channels. Bestrophin genes share a similar gene structure with highly conserved exon-intron boundaries, but with distinct 3' ends. Bestrophins are transmembrane proteins that contain a homologous region rich in aromatic residues, including an invariant arg-phe-pro motif. Mutation in one of the family members (bestrophin 1) is associated with vitelliform macular dystrophy. The bestrophin 2 gene is mainly expressed in the retinal pigment epithelium and colon. [provided by RefSeq, Jul 2008]","start":12751702,"end":12758458,"strand":1,"description":"bestrophin 2 [Source:HGNC Symbol;Acc:HGNC:17107]"}, {"versioned_ensembl_gene_id":"ENSG00000112293.14","gene_symbol":"GPLD1","gene_name":"glycosylphosphatidylinositol specific phospholipase D1 [Source:HGNC Symbol;Acc:HGNC:4459]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2822","summary":"Many proteins are tethered to the extracellular face of eukaryotic plasma membranes by a glycosylphosphatidylinositol (GPI) anchor. The GPI-anchor is a glycolipid found on many blood cells. The protein encoded by this gene is a GPI degrading enzyme. Glycosylphosphatidylinositol specific phospholipase D1 hydrolyzes the inositol phosphate linkage in proteins anchored by phosphatidylinositol glycans, thereby releasing the attached protein from the plasma membrane. [provided by RefSeq, Jul 2008]","start":24424565,"end":24495205,"strand":-1,"description":"glycosylphosphatidylinositol specific phospholipase D1 [Source:HGNC Symbol;Acc:HGNC:4459]"}, {"versioned_ensembl_gene_id":"ENSG00000151239.13","gene_symbol":"TWF1","gene_name":"twinfilin actin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9620]","synonyms":"A6,PTK9","biotype":"protein_coding","ncbi_id":"5756","summary":"This gene encodes twinfilin, an actin monomer-binding protein conserved from yeast to mammals. Studies of the mouse counterpart suggest that this protein may be an actin monomer-binding protein, and its localization to cortical G-actin-rich structures may be regulated by the small GTPase RAC1. [provided by RefSeq, Jul 2008]","start":43793723,"end":43806375,"strand":-1,"description":"twinfilin actin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9620]"}, {"versioned_ensembl_gene_id":"ENSG00000214273.4","gene_symbol":"AGGF1P1","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38051]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132380","summary":null,"start":190041342,"end":190043414,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38051]"}, {"versioned_ensembl_gene_id":"ENSG00000233734.8","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"C6orf16,SEEK1","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31193274,"end":31218582,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000237165.2","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31193614,"end":31198966,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000257777.1","gene_symbol":"AC022507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75600047,"end":75601551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238149.1","gene_symbol":"AC104978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28287235,"end":28287625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211632.4","gene_symbol":"IGKV3D-11","gene_name":"immunoglobulin kappa variable 3D-11 [Source:HGNC Symbol;Acc:HGNC:5823]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28876","summary":null,"start":90172802,"end":90173414,"strand":1,"description":"immunoglobulin kappa variable 3D-11 [Source:HGNC Symbol;Acc:HGNC:5823]"}, {"versioned_ensembl_gene_id":"ENSG00000095970.16","gene_symbol":"TREM2","gene_name":"triggering receptor expressed on myeloid cells 2 [Source:HGNC Symbol;Acc:HGNC:17761]","synonyms":"Trem2b,Trem2a,TREM-2,Trem2c","biotype":"protein_coding","ncbi_id":"54209","summary":"This gene encodes a membrane protein that forms a receptor signaling complex with the TYRO protein tyrosine kinase binding protein. The encoded protein functions in immune response and may be involved in chronic inflammation by triggering the production of constitutive inflammatory cytokines. Defects in this gene are a cause of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]","start":41158506,"end":41163186,"strand":-1,"description":"triggering receptor expressed on myeloid cells 2 [Source:HGNC Symbol;Acc:HGNC:17761]"}, {"versioned_ensembl_gene_id":"ENSG00000248694.1","gene_symbol":"AC079226.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":182772565,"end":182773931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186591.11","gene_symbol":"UBE2H","gene_name":"ubiquitin conjugating enzyme E2 H [Source:HGNC Symbol;Acc:HGNC:12484]","synonyms":"UBCH,UBC8,GID3","biotype":"protein_coding","ncbi_id":"7328","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein sequence is 100% identical to the mouse homolog and 98% identical to the frog and zebrafish homologs. Three alternatively spliced transcript variants have been found for this gene and they encode distinct isoforms. [provided by RefSeq, Feb 2011]","start":129830732,"end":129952949,"strand":-1,"description":"ubiquitin conjugating enzyme E2 H [Source:HGNC Symbol;Acc:HGNC:12484]"}, {"versioned_ensembl_gene_id":"ENSG00000235337.1","gene_symbol":"AC093083.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220127546,"end":220212491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282690.1","gene_symbol":"AL391421.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77866875,"end":77869610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000042980.12","gene_symbol":"ADAM28","gene_name":"ADAM metallopeptidase domain 28 [Source:HGNC Symbol;Acc:HGNC:206]","synonyms":"eMDCII,ADAM23,MDC-Ls,MDC-Lm","biotype":"protein_coding","ncbi_id":"10863","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene is a lymphocyte-expressed ADAM protein. This gene is present in a gene cluster with other members of the ADAM family on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":24294040,"end":24359018,"strand":1,"description":"ADAM metallopeptidase domain 28 [Source:HGNC Symbol;Acc:HGNC:206]"}, {"versioned_ensembl_gene_id":"ENSG00000233540.1","gene_symbol":"DNM3-IT1","gene_name":"DNM3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41494]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874284","summary":null,"start":171864187,"end":171864687,"strand":1,"description":"DNM3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41494]"}, {"versioned_ensembl_gene_id":"ENSG00000279786.1","gene_symbol":"AC105235.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":140820599,"end":140822414,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226060.7","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30174734,"end":30203710,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000225109.1","gene_symbol":"CR388382.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30177077,"end":30178900,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146038.11","gene_symbol":"DCDC2","gene_name":"doublecortin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18141]","synonyms":"RU2,NPHP19,KIAA1154,DFNB66,DCDC2A","biotype":"protein_coding","ncbi_id":"51473","summary":"This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013]","start":24171756,"end":24358052,"strand":-1,"description":"doublecortin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18141]"}, {"versioned_ensembl_gene_id":"ENSG00000248660.1","gene_symbol":"SRIP1","gene_name":"sorcin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11293]","synonyms":"SRIL","biotype":"processed_pseudogene","ncbi_id":"6644","summary":null,"start":58103147,"end":58103434,"strand":1,"description":"sorcin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11293]"}, {"versioned_ensembl_gene_id":"ENSG00000011198.7","gene_symbol":"ABHD5","gene_name":"abhydrolase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21396]","synonyms":"NCIE2,CGI-58","biotype":"protein_coding","ncbi_id":"51099","summary":"The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation. [provided by RefSeq, Jul 2008]","start":43690113,"end":43734371,"strand":1,"description":"abhydrolase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21396]"}, {"versioned_ensembl_gene_id":"ENSG00000088179.8","gene_symbol":"PTPN4","gene_name":"protein tyrosine phosphatase, non-receptor type 4 [Source:HGNC Symbol;Acc:HGNC:9656]","synonyms":"PTPMEG","biotype":"protein_coding","ncbi_id":"5775","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This protein contains a C-terminal PTP domain and an N-terminal domain homologous to the band 4.1 superfamily of cytoskeletal-associated proteins. This PTP has been shown to interact with glutamate receptor delta 2 and epsilon subunits, and is thought to play a role in signalling downstream of the glutamate receptors through tyrosine dephosphorylation. [provided by RefSeq, Jul 2008]","start":119759631,"end":119983818,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 4 [Source:HGNC Symbol;Acc:HGNC:9656]"}, {"versioned_ensembl_gene_id":"ENSG00000171724.2","gene_symbol":"VAT1L","gene_name":"vesicle amine transport 1 like [Source:HGNC Symbol;Acc:HGNC:29315]","synonyms":"KIAA1576","biotype":"protein_coding","ncbi_id":"57687","summary":null,"start":77788530,"end":77980107,"strand":1,"description":"vesicle amine transport 1 like [Source:HGNC Symbol;Acc:HGNC:29315]"}, {"versioned_ensembl_gene_id":"ENSG00000230450.1","gene_symbol":"NEK2P4","gene_name":"NEK2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100381202","summary":null,"start":131177618,"end":131178946,"strand":-1,"description":"NEK2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37818]"}, {"versioned_ensembl_gene_id":"ENSG00000236332.1","gene_symbol":"AP001604.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27361164,"end":27395787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047932.13","gene_symbol":"GOPC","gene_name":"golgi associated PDZ and coiled-coil motif containing [Source:HGNC Symbol;Acc:HGNC:17643]","synonyms":"PIST,GOPC1,FIG,dJ94G16.2,CAL","biotype":"protein_coding","ncbi_id":"57120","summary":"This gene encodes a Golgi protein with a PDZ domain. The PDZ domain is globular and proteins which contain them bind other proteins through short motifs near the C-termini. Mice which are deficient in the orthologous protein have globozoospermia and are infertile. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":117560269,"end":117602542,"strand":-1,"description":"golgi associated PDZ and coiled-coil motif containing [Source:HGNC Symbol;Acc:HGNC:17643]"}, {"versioned_ensembl_gene_id":"ENSG00000174013.7","gene_symbol":"FBXO45","gene_name":"F-box protein 45 [Source:HGNC Symbol;Acc:HGNC:29148]","synonyms":"Fbx45","biotype":"protein_coding","ncbi_id":"200933","summary":"Members of the F-box protein family, such as FBXO45, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (summary by Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Jan 2011]","start":196568611,"end":196589059,"strand":1,"description":"F-box protein 45 [Source:HGNC Symbol;Acc:HGNC:29148]"}, {"versioned_ensembl_gene_id":"ENSG00000282218.1","gene_symbol":"AL132671.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":117318211,"end":117573571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236516.1","gene_symbol":"KLF2P4","gene_name":"Kruppel like factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49283]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533668","summary":null,"start":131299220,"end":131300444,"strand":-1,"description":"Kruppel like factor 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49283]"}, {"versioned_ensembl_gene_id":"ENSG00000235563.1","gene_symbol":"AL445183.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53114576,"end":53118609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271607.1","gene_symbol":"Z84480.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110863860,"end":110864451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274047.4","gene_symbol":"SYNRG","gene_name":"synergin gamma [Source:HGNC Symbol;Acc:HGNC:557]","synonyms":"SYNG,MGC104959,AP1GBP1","biotype":"protein_coding","ncbi_id":"11276","summary":"This gene encodes a protein that interacts with the gamma subunit of AP1 clathrin-adaptor complex. The AP1 complex is located at the trans-Golgi network and associates specific proteins with clathrin-coated vesicles. This encoded protein may act to connect the AP1 complex to other proteins. Alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":37519433,"end":37614077,"strand":-1,"description":"synergin gamma [Source:HGNC Symbol;Acc:HGNC:557]"}, {"versioned_ensembl_gene_id":"ENSG00000162413.16","gene_symbol":"KLHL21","gene_name":"kelch like family member 21 [Source:HGNC Symbol;Acc:HGNC:29041]","synonyms":"KIAA0469","biotype":"protein_coding","ncbi_id":"9903","summary":null,"start":6590724,"end":6614607,"strand":-1,"description":"kelch like family member 21 [Source:HGNC Symbol;Acc:HGNC:29041]"}, {"versioned_ensembl_gene_id":"ENSG00000226158.1","gene_symbol":"CLCP2","gene_name":"Charcot-Leyden crystal protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42536]","synonyms":"LGALS10P1","biotype":"processed_pseudogene","ncbi_id":"100128145","summary":null,"start":114306646,"end":114307066,"strand":1,"description":"Charcot-Leyden crystal protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42536]"}, {"versioned_ensembl_gene_id":"ENSG00000255016.1","gene_symbol":"AC107918.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12025244,"end":12025598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267428.1","gene_symbol":"AC091135.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54566997,"end":54567303,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283247.1","gene_symbol":"AC096582.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":45860008,"end":45873082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264564.1","gene_symbol":"AC090897.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54525434,"end":54525563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131148.8","gene_symbol":"EMC8","gene_name":"ER membrane protein complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:7864]","synonyms":"NOC4,FAM158B,COX4NB,C16orf4,C16orf2","biotype":"protein_coding","ncbi_id":"10328","summary":null,"start":85771758,"end":85799608,"strand":-1,"description":"ER membrane protein complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:7864]"}, {"versioned_ensembl_gene_id":"ENSG00000264350.1","gene_symbol":"AC090897.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54406889,"end":54407114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224416.2","gene_symbol":"IFNA22P","gene_name":"interferon alpha 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:5431]","synonyms":"IFNAP22","biotype":"unprocessed_pseudogene","ncbi_id":"3453","summary":null,"start":21278050,"end":21278619,"strand":-1,"description":"interferon alpha 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:5431]"}, {"versioned_ensembl_gene_id":"ENSG00000140876.11","gene_symbol":"NUDT7","gene_name":"nudix hydrolase 7 [Source:HGNC Symbol;Acc:HGNC:8054]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283927","summary":"The protein encoded by this gene is a member of the Nudix hydrolase family. Nudix hydrolases eliminate potentially toxic nucleotide metabolites from the cell and regulate the concentrations and availability of many different nucleotide substrates, cofactors, and signaling molecules. Alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":77722492,"end":77742260,"strand":1,"description":"nudix hydrolase 7 [Source:HGNC Symbol;Acc:HGNC:8054]"}, {"versioned_ensembl_gene_id":"ENSG00000228083.2","gene_symbol":"IFNA14","gene_name":"interferon alpha 14 [Source:HGNC Symbol;Acc:HGNC:5420]","synonyms":"LEIF2H,IFN-alphaH","biotype":"protein_coding","ncbi_id":"3448","summary":null,"start":21239002,"end":21239991,"strand":-1,"description":"interferon alpha 14 [Source:HGNC Symbol;Acc:HGNC:5420]"}, {"versioned_ensembl_gene_id":"ENSG00000232138.1","gene_symbol":"IFNWP5","gene_name":"interferon omega 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5454]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392292","summary":null,"start":21231266,"end":21231853,"strand":-1,"description":"interferon omega 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5454]"}, {"versioned_ensembl_gene_id":"ENSG00000171522.5","gene_symbol":"PTGER4","gene_name":"prostaglandin E receptor 4 [Source:HGNC Symbol;Acc:HGNC:9596]","synonyms":"EP4","biotype":"protein_coding","ncbi_id":"5734","summary":"The protein encoded by this gene is a member of the G-protein coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). This receptor can activate T-cell factor signaling. It has been shown to mediate PGE2 induced expression of early growth response 1 (EGR1), regulate the level and stability of cyclooxygenase-2 mRNA, and lead to the phosphorylation of glycogen synthase kinase-3. Knockout studies in mice suggest that this receptor may be involved in the neonatal adaptation of circulatory system, osteoporosis, as well as initiation of skin immune responses. [provided by RefSeq, Jul 2008]","start":40679498,"end":40693735,"strand":1,"description":"prostaglandin E receptor 4 [Source:HGNC Symbol;Acc:HGNC:9596]"}, {"versioned_ensembl_gene_id":"ENSG00000187735.13","gene_symbol":"TCEA1","gene_name":"transcription elongation factor A1 [Source:HGNC Symbol;Acc:HGNC:11612]","synonyms":"TFIIS,TF2S,TCEA,SII,GTF2S","biotype":"protein_coding","ncbi_id":"6917","summary":null,"start":53966552,"end":54022529,"strand":-1,"description":"transcription elongation factor A1 [Source:HGNC Symbol;Acc:HGNC:11612]"}, {"versioned_ensembl_gene_id":"ENSG00000163170.11","gene_symbol":"BOLA3","gene_name":"bolA family member 3 [Source:HGNC Symbol;Acc:HGNC:24415]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388962","summary":"This gene encodes a protein that plays an essential role in the production of iron-sulfur (Fe-S) clusters for the normal maturation of lipoate-containing 2-oxoacid dehydrogenases, and for the assembly of the mitochondrial respiratory chain complexes. Mutation in this gene has been associated with multiple mitochondrial dysfunctions syndrome-2. Two alternatively spliced transcript variants encoding different isoforms with distinct subcellular localization have been reported for this gene (PMID:21944046). [provided by RefSeq, Dec 2011]","start":74135398,"end":74147994,"strand":-1,"description":"bolA family member 3 [Source:HGNC Symbol;Acc:HGNC:24415]"}, {"versioned_ensembl_gene_id":"ENSG00000145495.15","gene_symbol":"MARCH6","gene_name":"membrane associated ring-CH-type finger 6 [Source:HGNC Symbol;Acc:HGNC:30550]","synonyms":"TEB4,RNF176,MARCH-VI","biotype":"protein_coding","ncbi_id":"10299","summary":"This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":10353703,"end":10440388,"strand":1,"description":"membrane associated ring-CH-type finger 6 [Source:HGNC Symbol;Acc:HGNC:30550]"}, {"versioned_ensembl_gene_id":"ENSG00000269894.1","gene_symbol":"AC018809.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9935706,"end":9936258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196408.11","gene_symbol":"NOXO1","gene_name":"NADPH oxidase organizer 1 [Source:HGNC Symbol;Acc:HGNC:19404]","synonyms":"SNX28,SH3PXD5,P41NOXC,P41NOXB,P41NOXA","biotype":"protein_coding","ncbi_id":"124056","summary":"This gene encodes an NADPH oxidase (NOX) organizer, which positively regulates NOX1 and NOX3. The protein contains a PX domain and two SH3 domains. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012]","start":1978917,"end":1984192,"strand":-1,"description":"NADPH oxidase organizer 1 [Source:HGNC Symbol;Acc:HGNC:19404]"}, {"versioned_ensembl_gene_id":"ENSG00000141255.12","gene_symbol":"SPATA22","gene_name":"spermatogenesis associated 22 [Source:HGNC Symbol;Acc:HGNC:30705]","synonyms":"NYD-SP20","biotype":"protein_coding","ncbi_id":"84690","summary":null,"start":3440019,"end":3513852,"strand":-1,"description":"spermatogenesis associated 22 [Source:HGNC Symbol;Acc:HGNC:30705]"}, {"versioned_ensembl_gene_id":"ENSG00000243797.6","gene_symbol":"AC004917.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":106372251,"end":106770207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227472.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30142269,"end":30151257,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000253878.5","gene_symbol":"AC087752.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":94950037,"end":94951396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189339.11","gene_symbol":"SLC35E2B","gene_name":"solute carrier family 35 member E2B [Source:HGNC Symbol;Acc:HGNC:33941]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728661","summary":null,"start":1659529,"end":1692728,"strand":-1,"description":"solute carrier family 35 member E2B [Source:HGNC Symbol;Acc:HGNC:33941]"}, {"versioned_ensembl_gene_id":"ENSG00000123737.12","gene_symbol":"EXOSC9","gene_name":"exosome component 9 [Source:HGNC Symbol;Acc:HGNC:9137]","synonyms":"RRP45,PMSCL1,PM/Scl-75,p6,p5,Rrp45p","biotype":"protein_coding","ncbi_id":"5393","summary":"This gene encodes a component of the human exosome, a exoribonuclease complex which processes and degrades RNA in the nucleus and cytoplasm. This component may play a role in mRNA degradation and the polymyositis/scleroderma autoantigen complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":121801317,"end":121817021,"strand":1,"description":"exosome component 9 [Source:HGNC Symbol;Acc:HGNC:9137]"}, {"versioned_ensembl_gene_id":"ENSG00000255050.1","gene_symbol":"AC067930.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143573490,"end":143577397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223557.1","gene_symbol":"AL662834.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31871305,"end":31871598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118894.14","gene_symbol":"EEF2KMT","gene_name":"eukaryotic elongation factor 2 lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:32221]","synonyms":"SB153,MGC19636,FAM86A,EFM3","biotype":"protein_coding","ncbi_id":"196483","summary":null,"start":5084304,"end":5097808,"strand":-1,"description":"eukaryotic elongation factor 2 lysine methyltransferase [Source:HGNC Symbol;Acc:HGNC:32221]"}, {"versioned_ensembl_gene_id":"ENSG00000224314.1","gene_symbol":"AC005002.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117399452,"end":117400081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257800.1","gene_symbol":"FNBP1P1","gene_name":"formin binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44528]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533642","summary":null,"start":74120680,"end":74123218,"strand":1,"description":"formin binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44528]"}, {"versioned_ensembl_gene_id":"ENSG00000238066.1","gene_symbol":"AC005002.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117397938,"end":117398206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153993.13","gene_symbol":"SEMA3D","gene_name":"semaphorin 3D [Source:HGNC Symbol;Acc:HGNC:10726]","synonyms":"Sema-Z2,coll-2","biotype":"protein_coding","ncbi_id":"223117","summary":"This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016]","start":84995553,"end":85186855,"strand":-1,"description":"semaphorin 3D [Source:HGNC Symbol;Acc:HGNC:10726]"}, {"versioned_ensembl_gene_id":"ENSG00000280655.1","gene_symbol":"AC134981.1","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":21752278,"end":21752710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187912.11","gene_symbol":"CLEC17A","gene_name":"C-type lectin domain containing 17A [Source:HGNC Symbol;Acc:HGNC:34520]","synonyms":"FLJ45910","biotype":"protein_coding","ncbi_id":"388512","summary":null,"start":14583084,"end":14611157,"strand":1,"description":"C-type lectin domain containing 17A [Source:HGNC Symbol;Acc:HGNC:34520]"}, {"versioned_ensembl_gene_id":"ENSG00000259690.1","gene_symbol":"AC107980.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29373602,"end":29376956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279285.1","gene_symbol":"AP005264.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":12199345,"end":12200089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224600.5","gene_symbol":"AL031864.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171824610,"end":171824959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270914.1","gene_symbol":"AL096840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12017216,"end":12017308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258785.5","gene_symbol":"LINC01580","gene_name":"long intergenic non-protein coding RNA 1580 [Source:HGNC Symbol;Acc:HGNC:51414]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927129","summary":null,"start":93900701,"end":93984150,"strand":1,"description":"long intergenic non-protein coding RNA 1580 [Source:HGNC Symbol;Acc:HGNC:51414]"}, {"versioned_ensembl_gene_id":"ENSG00000138029.13","gene_symbol":"HADHB","gene_name":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit [Source:HGNC Symbol;Acc:HGNC:4803]","synonyms":"MTPB","biotype":"protein_coding","ncbi_id":"3032","summary":"This gene encodes the beta subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the beta subunit catalyzing the 3-ketoacyl-CoA thiolase activity. The encoded protein can also bind RNA and decreases the stability of some mRNAs. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. Mutations in this gene result in trifunctional protein deficiency. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]","start":26243170,"end":26290468,"strand":1,"description":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit [Source:HGNC Symbol;Acc:HGNC:4803]"}, {"versioned_ensembl_gene_id":"ENSG00000167483.17","gene_symbol":"FAM129C","gene_name":"family with sequence similarity 129 member C [Source:HGNC Symbol;Acc:HGNC:24130]","synonyms":"FLJ39802,BCNP1","biotype":"protein_coding","ncbi_id":"199786","summary":null,"start":17523301,"end":17553839,"strand":1,"description":"family with sequence similarity 129 member C [Source:HGNC Symbol;Acc:HGNC:24130]"}, {"versioned_ensembl_gene_id":"ENSG00000204904.7","gene_symbol":"LINC01545","gene_name":"long intergenic non-protein coding RNA 1545 [Source:HGNC Symbol;Acc:HGNC:17986]","synonyms":"OTTHUMG00000021429,CXorf31","biotype":"lincRNA","ncbi_id":"724087","summary":null,"start":46887417,"end":46899703,"strand":-1,"description":"long intergenic non-protein coding RNA 1545 [Source:HGNC Symbol;Acc:HGNC:17986]"}, {"versioned_ensembl_gene_id":"ENSG00000226345.1","gene_symbol":"AC083822.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":196423322,"end":196423522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259726.1","gene_symbol":"CSPG4P11","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48363]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631254","summary":null,"start":84186752,"end":84197384,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48363]"}, {"versioned_ensembl_gene_id":"ENSG00000281151.2","gene_symbol":"KCNQ2","gene_name":"potassium voltage-gated channel subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:6296]","synonyms":"Kv7.2,KCNA11,HNSPC,ENB1,EBN1,EBN,BFNC","biotype":"protein_coding","ncbi_id":"3785","summary":"The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":63414903,"end":63466150,"strand":-1,"description":"potassium voltage-gated channel subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:6296]"}, {"versioned_ensembl_gene_id":"ENSG00000281914.1","gene_symbol":"AL353658.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63422269,"end":63424555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229761.1","gene_symbol":"RPS20P1","gene_name":"ribosomal protein S20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10408]","synonyms":"RPS20P","biotype":"processed_pseudogene","ncbi_id":"54025","summary":null,"start":35724747,"end":35725100,"strand":-1,"description":"ribosomal protein S20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10408]"}, {"versioned_ensembl_gene_id":"ENSG00000234585.6","gene_symbol":"CCT6P3","gene_name":"chaperonin containing TCP1 subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35137]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643180","summary":null,"start":65038354,"end":65074713,"strand":1,"description":"chaperonin containing TCP1 subunit 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:35137]"}, {"versioned_ensembl_gene_id":"ENSG00000260202.2","gene_symbol":"AL109954.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23481645,"end":23519054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130545.15","gene_symbol":"CRB3","gene_name":"crumbs 3, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:20237]","synonyms":"MGC17303","biotype":"protein_coding","ncbi_id":"92359","summary":"This gene encodes a member of the Crumbs family of proteins. This gene is widely expressed in epithelial tissues where the encoded protein isoforms play various roles such as the control of cytokinesis and ciliogenesis or the formation of tight junctions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":6463777,"end":6467221,"strand":1,"description":"crumbs 3, cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:20237]"}, {"versioned_ensembl_gene_id":"ENSG00000223671.2","gene_symbol":"RPL34P3","gene_name":"ribosomal protein L34 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10343]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54026","summary":null,"start":35472095,"end":35472432,"strand":-1,"description":"ribosomal protein L34 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10343]"}, {"versioned_ensembl_gene_id":"ENSG00000234703.1","gene_symbol":"AF015262.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35136638,"end":35139222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123091.4","gene_symbol":"RNF11","gene_name":"ring finger protein 11 [Source:HGNC Symbol;Acc:HGNC:10056]","synonyms":"Sid1669p,MGC51169,CGI-123","biotype":"protein_coding","ncbi_id":"26994","summary":"The protein encoded by this gene contains a RING-H2 finger motif, which is known to be important for protein-protein interactions. The expression of this gene has been shown to be induced by mutant RET proteins (MEN2A/MEN2B). The germline mutations in RET gene are known to be responsible for the development of multiple endocrine neoplasia (MEN). [provided by RefSeq, Jul 2008]","start":51236271,"end":51273455,"strand":1,"description":"ring finger protein 11 [Source:HGNC Symbol;Acc:HGNC:10056]"}, {"versioned_ensembl_gene_id":"ENSG00000228111.1","gene_symbol":"TPT1P2","gene_name":"tumor protein, translationally-controlled 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49294]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128483","summary":null,"start":208214724,"end":208222625,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49294]"}, {"versioned_ensembl_gene_id":"ENSG00000281993.1","gene_symbol":"AC093627.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70972,"end":95683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115165.9","gene_symbol":"CYTIP","gene_name":"cytohesin 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:9506]","synonyms":"PSCDBP,HE,CYTHIP,CYBR,CASP,B3-1","biotype":"protein_coding","ncbi_id":"9595","summary":"The protein encoded by this gene contains 2 leucine zipper domains and a putative C-terminal nuclear targeting signal, but does not have any hydrophobic regions. This protein is expressed weakly in resting NK and T cells. The encoded protein modulates the activation of ARF genes by CYTH1. This protein interacts with CYTH1 and SNX27 proteins and may act to sequester CYTH1 protein in the cytoplasm.[provided by RefSeq, Aug 2008]","start":157414619,"end":157488961,"strand":-1,"description":"cytohesin 1 interacting protein [Source:HGNC Symbol;Acc:HGNC:9506]"}, {"versioned_ensembl_gene_id":"ENSG00000141458.12","gene_symbol":"NPC1","gene_name":"NPC intracellular cholesterol transporter 1 [Source:HGNC Symbol;Acc:HGNC:7897]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4864","summary":"This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009]","start":23506184,"end":23586898,"strand":-1,"description":"NPC intracellular cholesterol transporter 1 [Source:HGNC Symbol;Acc:HGNC:7897]"}, {"versioned_ensembl_gene_id":"ENSG00000270518.2","gene_symbol":"AC008626.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22770937,"end":22771191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168653.10","gene_symbol":"NDUFS5","gene_name":"NADH:ubiquinone oxidoreductase subunit S5 [Source:HGNC Symbol;Acc:HGNC:7712]","synonyms":"CI-15k","biotype":"protein_coding","ncbi_id":"4725","summary":"This gene is a member of the NADH dehydrogenase (ubiquinone) iron-sulfur protein family. The encoded protein is a subunit of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 1, 4 and 17. [provided by RefSeq, May 2010]","start":39026318,"end":39034636,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S5 [Source:HGNC Symbol;Acc:HGNC:7712]"}, {"versioned_ensembl_gene_id":"ENSG00000185787.14","gene_symbol":"MORF4L1","gene_name":"mortality factor 4 like 1 [Source:HGNC Symbol;Acc:HGNC:16989]","synonyms":"MRG15,MORFRG15,MEAF3,HsT17725,Eaf3","biotype":"protein_coding","ncbi_id":"10933","summary":null,"start":78810487,"end":78898133,"strand":1,"description":"mortality factor 4 like 1 [Source:HGNC Symbol;Acc:HGNC:16989]"}, {"versioned_ensembl_gene_id":"ENSG00000237659.1","gene_symbol":"RNASEH2CP1","gene_name":"ribonuclease H2 subunit C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24117]","synonyms":"AYP1p1","biotype":"processed_pseudogene","ncbi_id":"386608","summary":null,"start":2789827,"end":2790328,"strand":1,"description":"ribonuclease H2 subunit C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24117]"}, {"versioned_ensembl_gene_id":"ENSG00000205822.10","gene_symbol":"TPTE2P6","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42644]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"374491","summary":null,"start":24408157,"end":24597676,"strand":1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42644]"}, {"versioned_ensembl_gene_id":"ENSG00000243711.1","gene_symbol":"AC103975.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78863247,"end":78863729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152778.8","gene_symbol":"IFIT5","gene_name":"interferon induced protein with tetratricopeptide repeats 5 [Source:HGNC Symbol;Acc:HGNC:13328]","synonyms":"RI58","biotype":"protein_coding","ncbi_id":"24138","summary":null,"start":89414586,"end":89421001,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 5 [Source:HGNC Symbol;Acc:HGNC:13328]"}, {"versioned_ensembl_gene_id":"ENSG00000251015.1","gene_symbol":"SLC25A30-AS1","gene_name":"SLC25A30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42795]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874259","summary":null,"start":45418162,"end":45420371,"strand":1,"description":"SLC25A30 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42795]"}, {"versioned_ensembl_gene_id":"ENSG00000260864.1","gene_symbol":"ABHD17AP7","gene_name":"abhydrolase domain containing 17A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38508]","synonyms":"FAM108A8P","biotype":"unprocessed_pseudogene","ncbi_id":"100133212","summary":null,"start":32726615,"end":32729537,"strand":-1,"description":"abhydrolase domain containing 17A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38508]"}, {"versioned_ensembl_gene_id":"ENSG00000248975.2","gene_symbol":"AL133372.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29952397,"end":30297043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257120.1","gene_symbol":"AL356756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29652809,"end":29657916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240602.7","gene_symbol":"AADACP1","gene_name":"arylacetamide deacetylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50305]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"201651","summary":null,"start":151770428,"end":151784894,"strand":1,"description":"arylacetamide deacetylase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50305]"}, {"versioned_ensembl_gene_id":"ENSG00000197953.5","gene_symbol":"AADACL2","gene_name":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]","synonyms":"MGC72001","biotype":"protein_coding","ncbi_id":"344752","summary":null,"start":151733916,"end":151761339,"strand":1,"description":"arylacetamide deacetylase like 2 [Source:HGNC Symbol;Acc:HGNC:24427]"}, {"versioned_ensembl_gene_id":"ENSG00000012822.15","gene_symbol":"CALCOCO1","gene_name":"calcium binding and coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:29306]","synonyms":"KIAA1536,Cocoa,calphoglin","biotype":"protein_coding","ncbi_id":"57658","summary":null,"start":53708517,"end":53727745,"strand":-1,"description":"calcium binding and coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:29306]"}, {"versioned_ensembl_gene_id":"ENSG00000258971.1","gene_symbol":"AC112693.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93301416,"end":93301647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275898.1","gene_symbol":"AC125603.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116580974,"end":116583672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248919.7","gene_symbol":"ATP5J2-PTCD1","gene_name":"ATP5J2-PTCD1 readthrough [Source:HGNC Symbol;Acc:HGNC:38844]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526740","summary":"This locus represents naturally occurring read-through transcription between the ATP5J2 (ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2) and PTCD1 (pentatricopeptide repeat domain 1) genes on chromosome 7. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":99419749,"end":99466197,"strand":-1,"description":"ATP5J2-PTCD1 readthrough [Source:HGNC Symbol;Acc:HGNC:38844]"}, {"versioned_ensembl_gene_id":"ENSG00000113389.15","gene_symbol":"NPR3","gene_name":"natriuretic peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:7945]","synonyms":"NPRC,GUCY2B,FLJ14054,C5orf23,ANPRC","biotype":"protein_coding","ncbi_id":"4883","summary":"This gene encodes one of three natriuretic peptide receptors. Natriutetic peptides are small peptides which regulate blood volume and pressure, pulmonary hypertension, and cardiac function as well as some metabolic and growth processes. The product of this gene encodes a natriuretic peptide receptor responsible for clearing circulating and extracellular natriuretic peptides through endocytosis of the receptor. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]","start":32689070,"end":32791724,"strand":1,"description":"natriuretic peptide receptor 3 [Source:HGNC Symbol;Acc:HGNC:7945]"}, {"versioned_ensembl_gene_id":"ENSG00000272821.1","gene_symbol":"U62317.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50523926,"end":50524780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235869.1","gene_symbol":"Z99127.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174922107,"end":174922440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004766.15","gene_symbol":"VPS50","gene_name":"VPS50, EARP/GARPII complex subunit [Source:HGNC Symbol;Acc:HGNC:25956]","synonyms":"VPS54L,KIAA1861,FLJ20097,DKFZp313I2429,CCDC132","biotype":"protein_coding","ncbi_id":"55610","summary":null,"start":93232340,"end":93361121,"strand":1,"description":"VPS50, EARP/GARPII complex subunit [Source:HGNC Symbol;Acc:HGNC:25956]"}, {"versioned_ensembl_gene_id":"ENSG00000237249.1","gene_symbol":"Z99127.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174892417,"end":174893155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231378.1","gene_symbol":"NDUFAF4P4","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44543]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128889","summary":null,"start":174849667,"end":174850168,"strand":-1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44543]"}, {"versioned_ensembl_gene_id":"ENSG00000162836.11","gene_symbol":"ACP6","gene_name":"acid phosphatase 6, lysophosphatidic [Source:HGNC Symbol;Acc:HGNC:29609]","synonyms":"LPAP,ACPL1","biotype":"protein_coding","ncbi_id":"51205","summary":"This gene encodes a member of the histidine acid phosphatase protein family. The encoded protein hydrolyzes lysophosphatidic acid, which is involved in G protein-coupled receptor signaling, lipid raft modulation, and in balancing lipid composition within the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2016]","start":147629652,"end":147670496,"strand":-1,"description":"acid phosphatase 6, lysophosphatidic [Source:HGNC Symbol;Acc:HGNC:29609]"}, {"versioned_ensembl_gene_id":"ENSG00000282538.1","gene_symbol":"AC105219.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143696014,"end":143700591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277126.2","gene_symbol":"AC105219.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143683161,"end":143685420,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231026.1","gene_symbol":"XKRYP4","gene_name":"XK related, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23911]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379031","summary":null,"start":23917241,"end":23917723,"strand":-1,"description":"XK related, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23911]"}, {"versioned_ensembl_gene_id":"ENSG00000241151.1","gene_symbol":"LINC02066","gene_name":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374158","summary":null,"start":151637174,"end":151657966,"strand":1,"description":"long intergenic non-protein coding RNA 2066 [Source:HGNC Symbol;Acc:HGNC:52911]"}, {"versioned_ensembl_gene_id":"ENSG00000173013.5","gene_symbol":"CCDC96","gene_name":"coiled-coil domain containing 96 [Source:HGNC Symbol;Acc:HGNC:26900]","synonyms":"FLJ90575","biotype":"protein_coding","ncbi_id":"257236","summary":null,"start":7040849,"end":7042939,"strand":-1,"description":"coiled-coil domain containing 96 [Source:HGNC Symbol;Acc:HGNC:26900]"}, {"versioned_ensembl_gene_id":"ENSG00000092201.9","gene_symbol":"SUPT16H","gene_name":"SPT16 homolog, facilitates chromatin remodeling subunit [Source:HGNC Symbol;Acc:HGNC:11465]","synonyms":"SPT16/CDC68,FLJ14010,FLJ10857,FACTP140,FACT,CDC68","biotype":"protein_coding","ncbi_id":"11198","summary":"Transcription of protein-coding genes can be reconstituted on naked DNA with only the general transcription factors and RNA polymerase II. However, this minimal system cannot transcribe DNA packaged into chromatin, indicating that accessory factors may facilitate access to DNA. One such factor, FACT (facilitates chromatin transcription), interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT is composed of an 80 kDa subunit and a 140 kDa subunit; this gene encodes the 140 kDa subunit. [provided by RefSeq, Feb 2009]","start":21351472,"end":21384266,"strand":-1,"description":"SPT16 homolog, facilitates chromatin remodeling subunit [Source:HGNC Symbol;Acc:HGNC:11465]"}, {"versioned_ensembl_gene_id":"ENSG00000226016.1","gene_symbol":"RPL36AP55","gene_name":"ribosomal protein L36a pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:44939]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420206","summary":null,"start":27904209,"end":27905162,"strand":1,"description":"ribosomal protein L36a pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:44939]"}, {"versioned_ensembl_gene_id":"ENSG00000106246.17","gene_symbol":"PTCD1","gene_name":"pentatricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:22198]","synonyms":"KIAA0632","biotype":"protein_coding","ncbi_id":"26024","summary":"This gene encodes a mitochondrial protein that binds leucine tRNAs and other mitochondrial RNAs and plays a role in the regulation of translation. Increased expression of this gene results in decreased mitochondrial leucine tRNA levels. Naturally occurring read-through transcription exists between upstream ATP5J2 (ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2) and this gene. [provided by RefSeq, Aug 2015]","start":99416739,"end":99466163,"strand":-1,"description":"pentatricopeptide repeat domain 1 [Source:HGNC Symbol;Acc:HGNC:22198]"}, {"versioned_ensembl_gene_id":"ENSG00000242810.1","gene_symbol":"MRPL42P6","gene_name":"mitochondrial ribosomal protein L42 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44533]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480794","summary":null,"start":151475804,"end":151476174,"strand":-1,"description":"mitochondrial ribosomal protein L42 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44533]"}, {"versioned_ensembl_gene_id":"ENSG00000281974.1","gene_symbol":"AC025268.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86948677,"end":86949875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272734.1","gene_symbol":"ADIRF-AS1","gene_name":"ADIRF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45127]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100133190","summary":null,"start":86965345,"end":86971311,"strand":-1,"description":"ADIRF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45127]"}, {"versioned_ensembl_gene_id":"ENSG00000173267.13","gene_symbol":"SNCG","gene_name":"synuclein gamma [Source:HGNC Symbol;Acc:HGNC:11141]","synonyms":"SR,persyn,BCSG1","biotype":"protein_coding","ncbi_id":"6623","summary":"This gene encodes a member of the synuclein family of proteins which are believed to be involved in the pathogenesis of neurodegenerative diseases. Mutations in this gene have also been associated with breast tumor development. [provided by RefSeq, Jan 2010]","start":86958618,"end":86963260,"strand":1,"description":"synuclein gamma [Source:HGNC Symbol;Acc:HGNC:11141]"}, {"versioned_ensembl_gene_id":"ENSG00000275008.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738018,"end":54752516,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000189372.4","gene_symbol":"AL034369.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":108383398,"end":108383993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236502.1","gene_symbol":"SIX3-AS1","gene_name":"SIX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40532]","synonyms":"SIX3OS","biotype":"lincRNA","ncbi_id":"100506108","summary":null,"start":44940154,"end":44941873,"strand":-1,"description":"SIX3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40532]"}, {"versioned_ensembl_gene_id":"ENSG00000240008.1","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"C6orf21,LY6G6D,G6f,NG32","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31694294,"end":31698004,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000267148.1","gene_symbol":"AC005777.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3775996,"end":3776182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196498.13","gene_symbol":"NCOR2","gene_name":"nuclear receptor corepressor 2 [Source:HGNC Symbol;Acc:HGNC:7673]","synonyms":"SMRTE,SMRT,CTG26,TRAC-1,TNRC14","biotype":"protein_coding","ncbi_id":"9612","summary":"This gene encodes a nuclear receptor co-repressor that mediates transcriptional silencing of certain target genes. The encoded protein is a member of a family of thyroid hormone- and retinoic acid receptor-associated co-repressors. This protein acts as part of a multisubunit complex which includes histone deacetylases to modify chromatin structure that prevents basal transcriptional activity of target genes. Aberrant expression of this gene is associated with certain cancers. Alternate splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Apr 2011]","start":124324415,"end":124567589,"strand":-1,"description":"nuclear receptor corepressor 2 [Source:HGNC Symbol;Acc:HGNC:7673]"}, {"versioned_ensembl_gene_id":"ENSG00000239293.1","gene_symbol":"OR9P1P","gene_name":"olfactory receptor family 9 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15097]","synonyms":"OR9P2P","biotype":"unprocessed_pseudogene","ncbi_id":"81382","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143047213,"end":143047580,"strand":-1,"description":"olfactory receptor family 9 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15097]"}, {"versioned_ensembl_gene_id":"ENSG00000242134.2","gene_symbol":"RPL5P13","gene_name":"ribosomal protein L5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37023]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270834","summary":null,"start":142286917,"end":142287625,"strand":-1,"description":"ribosomal protein L5 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:37023]"}, {"versioned_ensembl_gene_id":"ENSG00000150051.13","gene_symbol":"MKX","gene_name":"mohawk homeobox [Source:HGNC Symbol;Acc:HGNC:23729]","synonyms":"MGC39616,IRXL1,C10orf48","biotype":"protein_coding","ncbi_id":"283078","summary":"The protein encoded by this gene is an IRX family-related homeobox protein that may play a role in cell adhesion. Studies in mice suggest that this protein may be a regulator of tendon development. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Jun 2011]","start":27672875,"end":27746060,"strand":-1,"description":"mohawk homeobox [Source:HGNC Symbol;Acc:HGNC:23729]"}, {"versioned_ensembl_gene_id":"ENSG00000163497.2","gene_symbol":"FEV","gene_name":"FEV, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:18562]","synonyms":"Pet-1","biotype":"protein_coding","ncbi_id":"54738","summary":"This gene belongs to the ETS transcription factor family. ETS family members have a highly conserved 85-amino acid ETS domain that binds purine-rich DNA sequences. The alanine-rich C-terminus of this gene indicates that it may act as a transcription repressor. This gene is exclusively expressed in neurons of the central serotonin (5-HT) system, a system implicated in the pathogeny of such psychiatric diseases as depression, anxiety, and eating disorders. In some types of Ewing tumors, this gene is fused to the Ewing sarcoma (EWS) gene following chromosome translocations. [provided by RefSeq, Jul 2008]","start":218981087,"end":218985657,"strand":-1,"description":"FEV, ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:18562]"}, {"versioned_ensembl_gene_id":"ENSG00000230500.1","gene_symbol":"MKX-AS1","gene_name":"MKX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50686]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929202","summary":null,"start":27744786,"end":27767794,"strand":1,"description":"MKX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50686]"}, {"versioned_ensembl_gene_id":"ENSG00000234359.3","gene_symbol":"ELK1P1","gene_name":"ELK1, member of ETS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39021]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647102","summary":null,"start":45391626,"end":45392205,"strand":-1,"description":"ELK1, member of ETS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39021]"}, {"versioned_ensembl_gene_id":"ENSG00000283137.1","gene_symbol":"AC183088.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21543038,"end":21543920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135951.14","gene_symbol":"TSGA10","gene_name":"testis specific 10 [Source:HGNC Symbol;Acc:HGNC:14927]","synonyms":"CT79,CEP4L","biotype":"protein_coding","ncbi_id":"80705","summary":null,"start":98997261,"end":99154964,"strand":-1,"description":"testis specific 10 [Source:HGNC Symbol;Acc:HGNC:14927]"}, {"versioned_ensembl_gene_id":"ENSG00000283336.1","gene_symbol":"AC135068.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21609104,"end":21610016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224928.2","gene_symbol":"KRT8P30","gene_name":"keratin 8 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:33382]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391485","summary":null,"start":218953401,"end":218954050,"strand":-1,"description":"keratin 8 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:33382]"}, {"versioned_ensembl_gene_id":"ENSG00000240436.1","gene_symbol":"AC114982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62575951,"end":62576271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232305.1","gene_symbol":"CLCP1","gene_name":"Charcot-Leyden crystal protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19257]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266626","summary":null,"start":17424388,"end":17424775,"strand":-1,"description":"Charcot-Leyden crystal protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19257]"}, {"versioned_ensembl_gene_id":"ENSG00000242945.2","gene_symbol":"AC015524.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53605254,"end":53605725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080546.13","gene_symbol":"SESN1","gene_name":"sestrin 1 [Source:HGNC Symbol;Acc:HGNC:21595]","synonyms":"SEST1,PA26","biotype":"protein_coding","ncbi_id":"27244","summary":"This gene encodes a member of the sestrin family. Sestrins are induced by the p53 tumor suppressor protein and play a role in the cellular response to DNA damage and oxidative stress. The encoded protein mediates p53 inhibition of cell growth by activating AMP-activated protein kinase, which results in the inhibition of the mammalian target of rapamycin protein. The encoded protein also plays a critical role in antioxidant defense by regenerating overoxidized peroxiredoxins, and the expression of this gene is a potential marker for exposure to radiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":108986437,"end":109094819,"strand":-1,"description":"sestrin 1 [Source:HGNC Symbol;Acc:HGNC:21595]"}, {"versioned_ensembl_gene_id":"ENSG00000211655.3","gene_symbol":"IGLV1-36","gene_name":"immunoglobulin lambda variable 1-36 [Source:HGNC Symbol;Acc:HGNC:5876]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28826","summary":null,"start":22431958,"end":22432465,"strand":1,"description":"immunoglobulin lambda variable 1-36 [Source:HGNC Symbol;Acc:HGNC:5876]"}, {"versioned_ensembl_gene_id":"ENSG00000253889.1","gene_symbol":"IGLVI-38","gene_name":"immunoglobulin lambda variable (I)-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5935]","synonyms":"IGLV(I)-38","biotype":"IG_V_pseudogene","ncbi_id":"28768","summary":null,"start":22425821,"end":22426314,"strand":1,"description":"immunoglobulin lambda variable (I)-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5935]"}, {"versioned_ensembl_gene_id":"ENSG00000279663.2","gene_symbol":"AC104623.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16541690,"end":16545695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260326.1","gene_symbol":"PHBP21","gene_name":"prohibitin pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390730","summary":null,"start":52934813,"end":52935635,"strand":1,"description":"prohibitin pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51554]"}, {"versioned_ensembl_gene_id":"ENSG00000213362.3","gene_symbol":"FTH1P12","gene_name":"ferritin heavy chain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:3982]","synonyms":"FTHL12","biotype":"processed_pseudogene","ncbi_id":"2504","summary":null,"start":15527133,"end":15527683,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:3982]"}, {"versioned_ensembl_gene_id":"ENSG00000219135.1","gene_symbol":"RPL23AP48","gene_name":"ribosomal protein L23a pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36110]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728567","summary":null,"start":121679972,"end":121680459,"strand":-1,"description":"ribosomal protein L23a pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:36110]"}, {"versioned_ensembl_gene_id":"ENSG00000233866.1","gene_symbol":"AC145543.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15914721,"end":15915800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083642.18","gene_symbol":"PDS5B","gene_name":"PDS5 cohesin associated factor B [Source:HGNC Symbol;Acc:HGNC:20418]","synonyms":"KIAA0979,FLJ23236,CG008,AS3,APRIN","biotype":"protein_coding","ncbi_id":"23047","summary":"This gene encodes a protein that interacts with the conserved protein complex termed cohesin. The cohesin complex holds together sister chromatids and facilitates accurate chromosome segregation during mitosis and meiosis. This protein is also a negative regulator of cell proliferation and may be a tumor-suppressor gene. [provided by RefSeq, Jul 2015]","start":32586427,"end":32778019,"strand":1,"description":"PDS5 cohesin associated factor B [Source:HGNC Symbol;Acc:HGNC:20418]"}, {"versioned_ensembl_gene_id":"ENSG00000268942.2","gene_symbol":"CKS1BP3","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:24233]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246715","summary":null,"start":62512246,"end":62512482,"strand":-1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:24233]"}, {"versioned_ensembl_gene_id":"ENSG00000224438.3","gene_symbol":"RPL23AP14","gene_name":"ribosomal protein L23a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:21007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341511","summary":null,"start":2781904,"end":2782371,"strand":1,"description":"ribosomal protein L23a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:21007]"}, {"versioned_ensembl_gene_id":"ENSG00000231728.3","gene_symbol":"AC234782.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103917411,"end":103919548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196812.4","gene_symbol":"ZSCAN16","gene_name":"zinc finger and SCAN domain containing 16 [Source:HGNC Symbol;Acc:HGNC:20813]","synonyms":"ZNF435,ZNF392,FLJ22191,dJ265C24.3","biotype":"protein_coding","ncbi_id":"80345","summary":null,"start":28124560,"end":28130082,"strand":1,"description":"zinc finger and SCAN domain containing 16 [Source:HGNC Symbol;Acc:HGNC:20813]"}, {"versioned_ensembl_gene_id":"ENSG00000279707.1","gene_symbol":"AC120349.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47866839,"end":47867367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141485.16","gene_symbol":"SLC13A5","gene_name":"solute carrier family 13 member 5 [Source:HGNC Symbol;Acc:HGNC:23089]","synonyms":"NACT","biotype":"protein_coding","ncbi_id":"284111","summary":"This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":6684713,"end":6713567,"strand":-1,"description":"solute carrier family 13 member 5 [Source:HGNC Symbol;Acc:HGNC:23089]"}, {"versioned_ensembl_gene_id":"ENSG00000123130.16","gene_symbol":"ACOT9","gene_name":"acyl-CoA thioesterase 9 [Source:HGNC Symbol;Acc:HGNC:17152]","synonyms":"MT-ACT48,CGI-16,ACATE2","biotype":"protein_coding","ncbi_id":"23597","summary":"The protein encoded by this gene is a mitochondrial acyl-CoA thioesterase of unknown function. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":23702253,"end":23766475,"strand":-1,"description":"acyl-CoA thioesterase 9 [Source:HGNC Symbol;Acc:HGNC:17152]"}, {"versioned_ensembl_gene_id":"ENSG00000260685.1","gene_symbol":"AC027104.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75950464,"end":75951144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170381.12","gene_symbol":"SEMA3E","gene_name":"semaphorin 3E [Source:HGNC Symbol;Acc:HGNC:10727]","synonyms":"SEMAH,M-SemaK,KIAA0331,coll-5","biotype":"protein_coding","ncbi_id":"9723","summary":"Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. This gene encodes a class 4 semaphorin. This gene encodes a class 3 semaphorin. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":83363906,"end":83649010,"strand":-1,"description":"semaphorin 3E [Source:HGNC Symbol;Acc:HGNC:10727]"}, {"versioned_ensembl_gene_id":"ENSG00000279851.2","gene_symbol":"CR382287.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10122273,"end":10129029,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235503.2","gene_symbol":"AC079799.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":83355154,"end":83362266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273618.1","gene_symbol":"AL135999.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23530682,"end":23532367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157306.14","gene_symbol":"ZFHX2-AS1","gene_name":"ZFHX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52658]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"109729160","summary":null,"start":23511760,"end":23560778,"strand":1,"description":"ZFHX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52658]"}, {"versioned_ensembl_gene_id":"ENSG00000164885.12","gene_symbol":"CDK5","gene_name":"cyclin dependent kinase 5 [Source:HGNC Symbol;Acc:HGNC:1774]","synonyms":"PSSALRE","biotype":"protein_coding","ncbi_id":"1020","summary":"This gene encodes a proline-directed serine/threonine kinase that is a member of the cyclin-dependent kinase family of proteins. Unlike other members of the family, the protein encoded by this gene does not directly control cell cycle regulation. Instead the protein, which is predominantly expressed at high levels in mammalian postmitotic central nervous system neurons, functions in diverse processes such as synaptic plasticity and neuronal migration through phosphorylation of proteins required for cytoskeletal organization, endocytosis and exocytosis, and apoptosis. In humans, an allelic variant of the gene that results in undetectable levels of the protein has been associated with lethal autosomal recessive lissencephaly-7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015]","start":151053812,"end":151058530,"strand":-1,"description":"cyclin dependent kinase 5 [Source:HGNC Symbol;Acc:HGNC:1774]"}, {"versioned_ensembl_gene_id":"ENSG00000270533.2","gene_symbol":"CR382285.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":9975017,"end":10119309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278255.1","gene_symbol":"AC005344.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2217462,"end":2217920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115204.14","gene_symbol":"MPV17","gene_name":"MPV17, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:7224]","synonyms":"SYM1","biotype":"protein_coding","ncbi_id":"4358","summary":"This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS). [provided by RefSeq, Jul 2008]","start":27309492,"end":27325680,"strand":-1,"description":"MPV17, mitochondrial inner membrane protein [Source:HGNC Symbol;Acc:HGNC:7224]"}, {"versioned_ensembl_gene_id":"ENSG00000270196.1","gene_symbol":"AC007255.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29551521,"end":29552151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262187.1","gene_symbol":"AC137800.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32618733,"end":32618852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271378.1","gene_symbol":"C8orf59P2","gene_name":"chromosome 8 open reading frame 59 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480687","summary":null,"start":37130430,"end":37130700,"strand":1,"description":"chromosome 8 open reading frame 59 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51357]"}, {"versioned_ensembl_gene_id":"ENSG00000203784.2","gene_symbol":"LELP1","gene_name":"late cornified envelope like proline rich 1 [Source:HGNC Symbol;Acc:HGNC:32046]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149018","summary":null,"start":153203443,"end":153205120,"strand":1,"description":"late cornified envelope like proline rich 1 [Source:HGNC Symbol;Acc:HGNC:32046]"}, {"versioned_ensembl_gene_id":"ENSG00000241636.1","gene_symbol":"LINC01323","gene_name":"long intergenic non-protein coding RNA 1323 [Source:HGNC Symbol;Acc:HGNC:50529]","synonyms":"TCONS_00005874","biotype":"lincRNA","ncbi_id":"106635527","summary":null,"start":164670878,"end":164686076,"strand":-1,"description":"long intergenic non-protein coding RNA 1323 [Source:HGNC Symbol;Acc:HGNC:50529]"}, {"versioned_ensembl_gene_id":"ENSG00000228651.1","gene_symbol":"AC074327.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52556702,"end":52755409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240792.1","gene_symbol":"AC079910.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163475067,"end":163479365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233417.1","gene_symbol":"AC004872.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120141016,"end":120142996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225546.5","gene_symbol":"LINC02476","gene_name":"long intergenic non-protein coding RNA 2476 [Source:HGNC Symbol;Acc:HGNC:53419]","synonyms":"LVCAT5","biotype":"lincRNA","ncbi_id":"105375475","summary":null,"start":119704556,"end":119907375,"strand":-1,"description":"long intergenic non-protein coding RNA 2476 [Source:HGNC Symbol;Acc:HGNC:53419]"}, {"versioned_ensembl_gene_id":"ENSG00000229699.1","gene_symbol":"AL161636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153174518,"end":153191676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168004.9","gene_symbol":"HRASLS5","gene_name":"HRAS like suppressor family member 5 [Source:HGNC Symbol;Acc:HGNC:24978]","synonyms":"HRLP5","biotype":"protein_coding","ncbi_id":"117245","summary":null,"start":63461404,"end":63491194,"strand":-1,"description":"HRAS like suppressor family member 5 [Source:HGNC Symbol;Acc:HGNC:24978]"}, {"versioned_ensembl_gene_id":"ENSG00000223410.1","gene_symbol":"AL009050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40121041,"end":40126357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256484.1","gene_symbol":"AC140118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131366660,"end":131371059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163950.12","gene_symbol":"SLBP","gene_name":"stem-loop binding protein [Source:HGNC Symbol;Acc:HGNC:10904]","synonyms":"HBP","biotype":"protein_coding","ncbi_id":"7884","summary":"This gene encodes a protein that binds to the stem-loop structure in replication-dependent histone mRNAs. Histone mRNAs do not contain introns or polyadenylation signals, and are processed by endonucleolytic cleavage. The stem-loop structure is essential for efficient processing but this structure also controls the transport, translation and stability of histone mRNAs. Expression of the protein is regulated during the cell cycle, increasing more than 10-fold during the latter part of G1. [provided by RefSeq, Jul 2008]","start":1692800,"end":1712555,"strand":-1,"description":"stem-loop binding protein [Source:HGNC Symbol;Acc:HGNC:10904]"}, {"versioned_ensembl_gene_id":"ENSG00000159516.8","gene_symbol":"SPRR2G","gene_name":"small proline rich protein 2G [Source:HGNC Symbol;Acc:HGNC:11267]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6706","summary":null,"start":153149582,"end":153150869,"strand":-1,"description":"small proline rich protein 2G [Source:HGNC Symbol;Acc:HGNC:11267]"}, {"versioned_ensembl_gene_id":"ENSG00000260701.1","gene_symbol":"AC025284.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77433382,"end":77444336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276972.1","gene_symbol":"AC078880.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115332146,"end":115332566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237753.1","gene_symbol":"AC079922.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112641832,"end":112645690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120837.7","gene_symbol":"NFYB","gene_name":"nuclear transcription factor Y subunit beta [Source:HGNC Symbol;Acc:HGNC:7805]","synonyms":"NF-YB,HAP3,CBF-A","biotype":"protein_coding","ncbi_id":"4801","summary":"The protein encoded by this gene is one subunit of a trimeric complex, forming a highly conserved transcription factor that binds with high specificity to CCAAT motifs in the promoter regions in a variety of genes. This gene product, subunit B, forms a tight dimer with the C subunit, a prerequisite for subunit A association. The resulting trimer binds to DNA with high specificity and affinity. Subunits B and C each contain a histone-like motif. Observation of the histone nature of these subunits is supported by two types of evidence; protein sequence alignments and experiments with mutants. [provided by RefSeq, Jul 2008]","start":104117077,"end":104138289,"strand":-1,"description":"nuclear transcription factor Y subunit beta [Source:HGNC Symbol;Acc:HGNC:7805]"}, {"versioned_ensembl_gene_id":"ENSG00000255101.1","gene_symbol":"AC103843.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42705583,"end":42721946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175691.8","gene_symbol":"ZNF77","gene_name":"zinc finger protein 77 [Source:HGNC Symbol;Acc:HGNC:13150]","synonyms":"pT1","biotype":"protein_coding","ncbi_id":"58492","summary":null,"start":2933218,"end":2944971,"strand":-1,"description":"zinc finger protein 77 [Source:HGNC Symbol;Acc:HGNC:13150]"}, {"versioned_ensembl_gene_id":"ENSG00000257954.1","gene_symbol":"AC125611.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49389516,"end":49390162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277479.1","gene_symbol":"AL022345.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42578500,"end":42578727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260433.1","gene_symbol":"LINC01917","gene_name":"long intergenic non-protein coding RNA 1917 [Source:HGNC Symbol;Acc:HGNC:52736]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928167","summary":null,"start":53579623,"end":53581059,"strand":-1,"description":"long intergenic non-protein coding RNA 1917 [Source:HGNC Symbol;Acc:HGNC:52736]"}, {"versioned_ensembl_gene_id":"ENSG00000234122.1","gene_symbol":"TRBV22OR9-2","gene_name":"T-cell receptor beta variable 22/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18740]","synonyms":"TRBV22/OR9-2,TCRBV29S2O,TCRBV22S2","biotype":"TR_V_pseudogene","ncbi_id":"246283","summary":null,"start":33634111,"end":33634246,"strand":1,"description":"T-cell receptor beta variable 22/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:18740]"}, {"versioned_ensembl_gene_id":"ENSG00000214688.5","gene_symbol":"C10orf105","gene_name":"chromosome 10 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:20304]","synonyms":"FLJ00245","biotype":"protein_coding","ncbi_id":"414152","summary":null,"start":71711702,"end":71737824,"strand":-1,"description":"chromosome 10 open reading frame 105 [Source:HGNC Symbol;Acc:HGNC:20304]"}, {"versioned_ensembl_gene_id":"ENSG00000100221.10","gene_symbol":"JOSD1","gene_name":"Josephin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28953]","synonyms":"KIAA0063","biotype":"protein_coding","ncbi_id":"9929","summary":null,"start":38685543,"end":38701556,"strand":-1,"description":"Josephin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28953]"}, {"versioned_ensembl_gene_id":"ENSG00000272438.1","gene_symbol":"AL645608.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":904834,"end":915976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241180.1","gene_symbol":"AL645608.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":914171,"end":914971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125611.15","gene_symbol":"CHCHD5","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17840]","synonyms":"MIC14,MGC11104,C2orf9","biotype":"protein_coding","ncbi_id":"84269","summary":null,"start":112584240,"end":112589275,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 5 [Source:HGNC Symbol;Acc:HGNC:17840]"}, {"versioned_ensembl_gene_id":"ENSG00000228251.1","gene_symbol":"AC012442.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":112590796,"end":112591939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229346.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30142335,"end":30151326,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000230368.2","gene_symbol":"FAM41C","gene_name":"family with sequence similarity 41 member C [Source:HGNC Symbol;Acc:HGNC:27635]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284593","summary":null,"start":868071,"end":876903,"strand":-1,"description":"family with sequence similarity 41 member C [Source:HGNC Symbol;Acc:HGNC:27635]"}, {"versioned_ensembl_gene_id":"ENSG00000234711.1","gene_symbol":"TUBB8P11","gene_name":"tubulin beta 8 class VIII pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:32337]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"388579","summary":null,"start":873292,"end":874349,"strand":1,"description":"tubulin beta 8 class VIII pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:32337]"}, {"versioned_ensembl_gene_id":"ENSG00000134709.10","gene_symbol":"HOOK1","gene_name":"hook microtubule tethering protein 1 [Source:HGNC Symbol;Acc:HGNC:19884]","synonyms":"HK1","biotype":"protein_coding","ncbi_id":"51361","summary":"This gene encodes a member of the hook family of coiled-coil proteins, which bind to microtubules and organelles through their N- and C-terminal domains, respectively. The encoded protein localizes to discrete punctuate subcellular structures, and interacts with several members of the Rab GTPase family involved in endocytosis. It is thought to link endocytic membrane trafficking to the microtubule cytoskeleton. Several alternatively spliced transcript variants have been identified, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":59814786,"end":59876378,"strand":1,"description":"hook microtubule tethering protein 1 [Source:HGNC Symbol;Acc:HGNC:19884]"}, {"versioned_ensembl_gene_id":"ENSG00000280562.1","gene_symbol":"AL132838.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93223598,"end":93224139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275947.2","gene_symbol":"TMEM251","gene_name":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]","synonyms":"DKFZP564F1123,C14orf109","biotype":"protein_coding","ncbi_id":"26175","summary":null,"start":93184951,"end":93187089,"strand":1,"description":"transmembrane protein 251 [Source:HGNC Symbol;Acc:HGNC:20218]"}, {"versioned_ensembl_gene_id":"ENSG00000145020.15","gene_symbol":"AMT","gene_name":"aminomethyltransferase [Source:HGNC Symbol;Acc:HGNC:473]","synonyms":"NKH,GCST","biotype":"protein_coding","ncbi_id":"275","summary":"This gene encodes one of four critical components of the glycine cleavage system. Mutations in this gene have been associated with glycine encephalopathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":49416775,"end":49422753,"strand":-1,"description":"aminomethyltransferase [Source:HGNC Symbol;Acc:HGNC:473]"}, {"versioned_ensembl_gene_id":"ENSG00000150722.10","gene_symbol":"PPP1R1C","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 1C [Source:HGNC Symbol;Acc:HGNC:14940]","synonyms":"Inhibitor-1-like","biotype":"protein_coding","ncbi_id":"151242","summary":"Protein phosphatase-1 (PP1) is a major serine/threonine phosphatase that regulates a variety of cellular functions. PP1 consists of a catalytic subunit (see PPP1CA; MIM 176875) and regulatory subunits that determine the subcellular localization of PP1 or regulate its function. PPP1R1C belongs to a group of PP1 inhibitory subunits that are themselves regulated by phosphorylation (Wang et al., 2008 [PubMed 18310074]).[supplied by OMIM, Feb 2010]","start":181954241,"end":182131398,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 1C [Source:HGNC Symbol;Acc:HGNC:14940]"}, {"versioned_ensembl_gene_id":"ENSG00000102977.13","gene_symbol":"ACD","gene_name":"ACD, shelterin complex subunit and telomerase recruitment factor [Source:HGNC Symbol;Acc:HGNC:25070]","synonyms":"Tpp1,Tint1,Ptop,Pip1","biotype":"protein_coding","ncbi_id":"65057","summary":"This gene encodes a protein that is involved in telomere function. This protein is one of six core proteins in the telosome/shelterin telomeric complex, which functions to maintain telomere length and to protect telomere ends. Through its interaction with other components, this protein plays a key role in the assembly and stabilization of this complex, and it mediates the access of telomerase to the telomere. Multiple transcript variants encoding different isoforms have been found for this gene. This gene, which is also referred to as TPP1, is distinct from the unrelated TPP1 gene on chromosome 11, which encodes tripeptidyl-peptidase I. [provided by RefSeq, Jul 2008]","start":67657512,"end":67660815,"strand":-1,"description":"ACD, shelterin complex subunit and telomerase recruitment factor [Source:HGNC Symbol;Acc:HGNC:25070]"}, {"versioned_ensembl_gene_id":"ENSG00000240972.1","gene_symbol":"MIF","gene_name":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]","synonyms":"GLIF,GIF","biotype":"protein_coding","ncbi_id":"4282","summary":"This gene encodes a lymphokine involved in cell-mediated immunity, immunoregulation, and inflammation. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. This lymphokine and the JAB1 protein form a complex in the cytosol near the peripheral plasma membrane, which may indicate an additional role in integrin signaling pathways. [provided by RefSeq, Jul 2008]","start":23894004,"end":23895227,"strand":1,"description":"macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Source:HGNC Symbol;Acc:HGNC:7097]"}, {"versioned_ensembl_gene_id":"ENSG00000171960.10","gene_symbol":"PPIH","gene_name":"peptidylprolyl isomerase H [Source:HGNC Symbol;Acc:HGNC:14651]","synonyms":"USA-CYP,SnuCyp-20,MGC5016,CYPH,CYP-20","biotype":"protein_coding","ncbi_id":"10465","summary":"The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein is a specific component of the complex that includes pre-mRNA processing factors PRPF3, PRPF4, and PRPF18, as well as U4/U5/U6 tri-snRNP. This protein has been shown to possess PPIase activity and may act as a protein chaperone that mediates the interactions between different proteins inside the spliceosome. [provided by RefSeq, Jul 2008]","start":42658425,"end":42676758,"strand":1,"description":"peptidylprolyl isomerase H [Source:HGNC Symbol;Acc:HGNC:14651]"}, {"versioned_ensembl_gene_id":"ENSG00000111700.12","gene_symbol":"SLCO1B3","gene_name":"solute carrier organic anion transporter family member 1B3 [Source:HGNC Symbol;Acc:HGNC:10961]","synonyms":"SLC21A8,OATP8,OATP1B3","biotype":"protein_coding","ncbi_id":"28234","summary":"This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of endogenous and xenobiotic compounds and plays a critical role in bile acid and bilirubin transport. Mutations in this gene are a cause of Rotor type hyperbilirubinemia. Alternative splicing of this gene and the use of alternative promoters results in transcript variants encoding different isoforms that differ in their tissue specificity. [provided by RefSeq, Mar 2017]","start":20810702,"end":20916911,"strand":1,"description":"solute carrier organic anion transporter family member 1B3 [Source:HGNC Symbol;Acc:HGNC:10961]"}, {"versioned_ensembl_gene_id":"ENSG00000114209.14","gene_symbol":"PDCD10","gene_name":"programmed cell death 10 [Source:HGNC Symbol;Acc:HGNC:8761]","synonyms":"TFAR15,CCM3","biotype":"protein_coding","ncbi_id":"11235","summary":"This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":167683298,"end":167734939,"strand":-1,"description":"programmed cell death 10 [Source:HGNC Symbol;Acc:HGNC:8761]"}, {"versioned_ensembl_gene_id":"ENSG00000174137.12","gene_symbol":"FAM53A","gene_name":"family with sequence similarity 53 member A [Source:HGNC Symbol;Acc:HGNC:31860]","synonyms":"DNTNP","biotype":"protein_coding","ncbi_id":"152877","summary":null,"start":1617915,"end":1684302,"strand":-1,"description":"family with sequence similarity 53 member A [Source:HGNC Symbol;Acc:HGNC:31860]"}, {"versioned_ensembl_gene_id":"ENSG00000224136.1","gene_symbol":"AC007568.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117882859,"end":117883675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227588.2","gene_symbol":"CNTN4-AS2","gene_name":"CNTN4 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39986]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100873976","summary":null,"start":2110409,"end":2144241,"strand":-1,"description":"CNTN4 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39986]"}, {"versioned_ensembl_gene_id":"ENSG00000278548.4","gene_symbol":"ADAM18","gene_name":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]","synonyms":"tMDCIII,ADAM27","biotype":"protein_coding","ncbi_id":"8749","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature sperm surface protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":39429440,"end":39575001,"strand":1,"description":"ADAM metallopeptidase domain 18 [Source:HGNC Symbol;Acc:HGNC:196]"}, {"versioned_ensembl_gene_id":"ENSG00000236620.1","gene_symbol":"XKRYP3","gene_name":"XK related, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23910]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379030","summary":null,"start":23715922,"end":23726808,"strand":-1,"description":"XK related, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23910]"}, {"versioned_ensembl_gene_id":"ENSG00000106069.21","gene_symbol":"CHN2","gene_name":"chimerin 2 [Source:HGNC Symbol;Acc:HGNC:1944]","synonyms":"ARHGAP3,RhoGAP3","biotype":"protein_coding","ncbi_id":"1124","summary":"This gene encodes a guanosine triphosphate (GTP)-metabolizing protein that contains a phorbol-ester/diacylglycerol (DAG)-type zinc finger, a Rho-GAP domain, and an SH2 domain. The encoded protein translocates from the cytosol to the Golgi apparatus membrane upon binding by diacylglycerol (DAG). Activity of this protein is important in cell proliferation and migration, and expression changes in this gene have been detected in cancers. A mutation in this gene has also been associated with schizophrenia in men. Alternative transcript splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, May 2014]","start":29122274,"end":29514328,"strand":1,"description":"chimerin 2 [Source:HGNC Symbol;Acc:HGNC:1944]"}, {"versioned_ensembl_gene_id":"ENSG00000134538.2","gene_symbol":"SLCO1B1","gene_name":"solute carrier organic anion transporter family member 1B1 [Source:HGNC Symbol;Acc:HGNC:10959]","synonyms":"SLC21A6,OATP1B1,OATP-C,LST-1","biotype":"protein_coding","ncbi_id":"10599","summary":"This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of numerous endogenous compounds including bilirubin, 17-beta-glucuronosyl estradiol and leukotriene C4. This protein is also involved in the removal of drug compounds such as statins, bromosulfophthalein and rifampin from the blood into the hepatocytes. Polymorphisms in the gene encoding this protein are associated with impaired transporter function. [provided by RefSeq, Mar 2009]","start":21131202,"end":21239246,"strand":1,"description":"solute carrier organic anion transporter family member 1B1 [Source:HGNC Symbol;Acc:HGNC:10959]"}, {"versioned_ensembl_gene_id":"ENSG00000204634.12","gene_symbol":"TBC1D8","gene_name":"TBC1 domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17791]","synonyms":"VRP,HBLP1,GRAMD8,AD3","biotype":"protein_coding","ncbi_id":"11138","summary":null,"start":101007617,"end":101252866,"strand":-1,"description":"TBC1 domain family member 8 [Source:HGNC Symbol;Acc:HGNC:17791]"}, {"versioned_ensembl_gene_id":"ENSG00000230140.5","gene_symbol":"AC016738.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100972648,"end":100977161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124657.1","gene_symbol":"OR2B6","gene_name":"olfactory receptor family 2 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:8241]","synonyms":"OR6-31,OR5-41,OR5-40,OR2B6P,OR2B5,OR2B1P,OR2B1,dJ408B20.2","biotype":"protein_coding","ncbi_id":"26212","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":27957241,"end":27958182,"strand":1,"description":"olfactory receptor family 2 subfamily B member 6 [Source:HGNC Symbol;Acc:HGNC:8241]"}, {"versioned_ensembl_gene_id":"ENSG00000262647.3","gene_symbol":"OR9G4","gene_name":"olfactory receptor family 9 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:15322]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283189","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56753901,"end":56754885,"strand":-1,"description":"olfactory receptor family 9 subfamily G member 4 [Source:HGNC Symbol;Acc:HGNC:15322]"}, {"versioned_ensembl_gene_id":"ENSG00000257062.6","gene_symbol":"AC022335.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21047179,"end":21176895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256157.1","gene_symbol":"AC011604.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20845065,"end":20845260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232962.11","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-D0-alpha,HLA-DZA,HLA-DNA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":32926465,"end":32931899,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000185467.7","gene_symbol":"KPNA7","gene_name":"karyopherin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:21839]","synonyms":"IPOA8","biotype":"protein_coding","ncbi_id":"402569","summary":"The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC), which consists of 60-100 proteins. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion while larger molecules are transported by an active process. The protein encoded by this gene belongs to the importin alpha family, and is involved in nuclear protein import, but exhibits different nuclear localization signal binding specificity compared to other members of the family. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, Jul 2016]","start":99173574,"end":99207506,"strand":-1,"description":"karyopherin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:21839]"}, {"versioned_ensembl_gene_id":"ENSG00000245330.4","gene_symbol":"AP005717.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119867419,"end":119874488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273133.1","gene_symbol":"AC116651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15563698,"end":15564253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262191.1","gene_symbol":"OR9G9","gene_name":"olfactory receptor family 9 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:31940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"504191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56711466,"end":56712383,"strand":1,"description":"olfactory receptor family 9 subfamily G member 9 [Source:HGNC Symbol;Acc:HGNC:31940]"}, {"versioned_ensembl_gene_id":"ENSG00000261958.1","gene_symbol":"OR9G1","gene_name":"olfactory receptor family 9 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:15319]","synonyms":"OR9G5","biotype":"protein_coding","ncbi_id":"390174","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56700386,"end":56701303,"strand":1,"description":"olfactory receptor family 9 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:15319]"}, {"versioned_ensembl_gene_id":"ENSG00000147586.9","gene_symbol":"MRPS28","gene_name":"mitochondrial ribosomal protein S28 [Source:HGNC Symbol;Acc:HGNC:14513]","synonyms":"MRPS35,MRP-S28,HSPC007","biotype":"protein_coding","ncbi_id":"28957","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that has been called mitochondrial ribosomal protein S35 in the literature. [provided by RefSeq, Jul 2008]","start":79918717,"end":80030289,"strand":-1,"description":"mitochondrial ribosomal protein S28 [Source:HGNC Symbol;Acc:HGNC:14513]"}, {"versioned_ensembl_gene_id":"ENSG00000124664.10","gene_symbol":"SPDEF","gene_name":"SAM pointed domain containing ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:17257]","synonyms":"PDEF,bA375E1.3","biotype":"protein_coding","ncbi_id":"25803","summary":"The protein encoded by this gene belongs to the ETS family of transcription factors. It is highly expressed in the prostate epithelial cells, and functions as an androgen-independent transactivator of prostate-specific antigen (PSA) promoter. Higher expression of this protein has also been reported in brain, breast, lung and ovarian tumors, compared to the corresponding normal tissues, and it shows better tumor-association than other cancer-associated molecules, making it a more suitable target for developing specific cancer therapies. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":34537802,"end":34556333,"strand":-1,"description":"SAM pointed domain containing ETS transcription factor [Source:HGNC Symbol;Acc:HGNC:17257]"}, {"versioned_ensembl_gene_id":"ENSG00000171443.6","gene_symbol":"ZNF524","gene_name":"zinc finger protein 524 [Source:HGNC Symbol;Acc:HGNC:28322]","synonyms":"MGC23143","biotype":"protein_coding","ncbi_id":"147807","summary":null,"start":55600022,"end":55603138,"strand":1,"description":"zinc finger protein 524 [Source:HGNC Symbol;Acc:HGNC:28322]"}, {"versioned_ensembl_gene_id":"ENSG00000128340.14","gene_symbol":"RAC2","gene_name":"ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) [Source:HGNC Symbol;Acc:HGNC:9802]","synonyms":"EN-7","biotype":"protein_coding","ncbi_id":"5880","summary":"This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013]","start":37225261,"end":37244448,"strand":-1,"description":"ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) [Source:HGNC Symbol;Acc:HGNC:9802]"}, {"versioned_ensembl_gene_id":"ENSG00000168126.3","gene_symbol":"OR2W6P","gene_name":"olfactory receptor family 2 subfamily W member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15072]","synonyms":"OR2W7P","biotype":"unprocessed_pseudogene","ncbi_id":"81406","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":27937465,"end":27938403,"strand":1,"description":"olfactory receptor family 2 subfamily W member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15072]"}, {"versioned_ensembl_gene_id":"ENSG00000213657.3","gene_symbol":"RPL31P44","gene_name":"ribosomal protein L31 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:35523]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644522","summary":null,"start":52389112,"end":52389488,"strand":-1,"description":"ribosomal protein L31 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:35523]"}, {"versioned_ensembl_gene_id":"ENSG00000278974.1","gene_symbol":"AC093909.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":188740507,"end":188741281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225291.4","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29303399,"end":29304364,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000229045.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"bA150A6.3,DDX6P,DDX6-Lp","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29326337,"end":29327771,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000116661.10","gene_symbol":"FBXO2","gene_name":"F-box protein 2 [Source:HGNC Symbol;Acc:HGNC:13581]","synonyms":"OCP1,Nfb42,FBX2,Fbs1,Fbg1","biotype":"protein_coding","ncbi_id":"26232","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. This protein is highly similar to the rat NFB42 (neural F Box 42 kDa) protein which is enriched in the nervous system and may play a role in maintaining neurons in a postmitotic state. [provided by RefSeq, Jul 2008]","start":11637018,"end":11655785,"strand":-1,"description":"F-box protein 2 [Source:HGNC Symbol;Acc:HGNC:13581]"}, {"versioned_ensembl_gene_id":"ENSG00000159961.2","gene_symbol":"OR3A3","gene_name":"olfactory receptor family 3 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8284]","synonyms":"OR3A8P,OR3A7,OR3A6,OR17-201,OR17-16,OR17-137","biotype":"protein_coding","ncbi_id":"8392","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3411370,"end":3424070,"strand":1,"description":"olfactory receptor family 3 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8284]"}, {"versioned_ensembl_gene_id":"ENSG00000176209.11","gene_symbol":"SMIM19","gene_name":"small integral membrane protein 19 [Source:HGNC Symbol;Acc:HGNC:25166]","synonyms":"C8orf40","biotype":"protein_coding","ncbi_id":"114926","summary":null,"start":42541155,"end":42555193,"strand":1,"description":"small integral membrane protein 19 [Source:HGNC Symbol;Acc:HGNC:25166]"}, {"versioned_ensembl_gene_id":"ENSG00000243480.7","gene_symbol":"AMY2A","gene_name":"amylase, alpha 2A (pancreatic) [Source:HGNC Symbol;Acc:HGNC:477]","synonyms":"AMY2","biotype":"protein_coding","ncbi_id":"279","summary":"This gene encodes a member of the alpha-amylase family of proteins. Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, catalyzing the first step in digestion of dietary starch and glycogen. This gene and several family members are present in a gene cluster on chromosome 1. This gene encodes an amylase isoenzyme produced by the pancreas. [provided by RefSeq, Jan 2015]","start":103616811,"end":103625780,"strand":1,"description":"amylase, alpha 2A (pancreatic) [Source:HGNC Symbol;Acc:HGNC:477]"}, {"versioned_ensembl_gene_id":"ENSG00000256199.1","gene_symbol":"AC078962.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64507166,"end":64533638,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236263.1","gene_symbol":"AC234582.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155211151,"end":155213819,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231754.2","gene_symbol":"AL512380.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21521678,"end":21523783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249269.1","gene_symbol":"AC093909.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188757679,"end":188778979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162924.13","gene_symbol":"REL","gene_name":"REL proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9954]","synonyms":"I-Rel,c-Rel","biotype":"protein_coding","ncbi_id":"5966","summary":"This gene encodes a protein that belongs to the Rel homology domain/immunoglobulin-like fold, plexin, transcription factor (RHD/IPT) family. Members of this family regulate genes involved in apoptosis, inflammation, the immune response, and oncogenic processes. This proto-oncogene plays a role in the survival and proliferation of B lymphocytes. Mutation or amplification of this gene is associated with B-cell lymphomas, including Hodgkin's lymphoma. Single nucleotide polymorphisms in this gene are associated with susceptibility to ulcerative colitis and rheumatoid arthritis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014]","start":60881521,"end":60931610,"strand":1,"description":"REL proto-oncogene, NF-kB subunit [Source:HGNC Symbol;Acc:HGNC:9954]"}, {"versioned_ensembl_gene_id":"ENSG00000225193.5","gene_symbol":"AC091167.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":90206572,"end":90206967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253330.1","gene_symbol":"AC024451.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47511034,"end":47512141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231021.9","gene_symbol":"CR788250.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32611143,"end":32626106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229431.1","gene_symbol":"AL139289.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43385113,"end":43389155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169231.13","gene_symbol":"THBS3","gene_name":"thrombospondin 3 [Source:HGNC Symbol;Acc:HGNC:11787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7059","summary":"The protein encoded by this gene belongs to the thrombospondin family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentameric molecule linked by a single disulfide bond. This gene shares a common promoter with metaxin 1. Alternate splicing results in coding and non-coding transcript variants. [provided by RefSeq, Nov 2011]","start":155195588,"end":155209051,"strand":-1,"description":"thrombospondin 3 [Source:HGNC Symbol;Acc:HGNC:11787]"}, {"versioned_ensembl_gene_id":"ENSG00000251619.1","gene_symbol":"LINC02508","gene_name":"long intergenic non-protein coding RNA 2508 [Source:HGNC Symbol;Acc:HGNC:53497]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377610","summary":null,"start":188776657,"end":188785511,"strand":1,"description":"long intergenic non-protein coding RNA 2508 [Source:HGNC Symbol;Acc:HGNC:53497]"}, {"versioned_ensembl_gene_id":"ENSG00000283480.1","gene_symbol":"AL512380.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21528739,"end":21595593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163406.10","gene_symbol":"SLC15A2","gene_name":"solute carrier family 15 member 2 [Source:HGNC Symbol;Acc:HGNC:10921]","synonyms":"PEPT2","biotype":"protein_coding","ncbi_id":"6565","summary":"The mammalian kidney expresses a proton-coupled peptide transporter that is responsible for the absorption of small peptides, as well as beta-lactam antibiotics and other peptide-like drugs, from the tubular filtrate. This transporter, SLC15A2, belongs to the same gene family as SLC15A1 (MIM 600544), the proton-coupled peptide transporter found in the small intestine (Liu et al, 1995 [PubMed 7756356]).[supplied by OMIM, Feb 2011]","start":121894089,"end":121944102,"strand":1,"description":"solute carrier family 15 member 2 [Source:HGNC Symbol;Acc:HGNC:10921]"}, {"versioned_ensembl_gene_id":"ENSG00000143195.12","gene_symbol":"ILDR2","gene_name":"immunoglobulin like domain containing receptor 2 [Source:HGNC Symbol;Acc:HGNC:18131]","synonyms":"C1orf32","biotype":"protein_coding","ncbi_id":"387597","summary":null,"start":166895711,"end":166975482,"strand":-1,"description":"immunoglobulin like domain containing receptor 2 [Source:HGNC Symbol;Acc:HGNC:18131]"}, {"versioned_ensembl_gene_id":"ENSG00000250626.2","gene_symbol":"AC093909.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188777679,"end":188796633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124766.6","gene_symbol":"SOX4","gene_name":"SRY-box 4 [Source:HGNC Symbol;Acc:HGNC:11200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6659","summary":"This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins, such as syndecan binding protein (syntenin). The protein may function in the apoptosis pathway leading to cell death as well as to tumorigenesis and may mediate downstream effects of parathyroid hormone (PTH) and PTH-related protein (PTHrP) in bone development. The solution structure has been resolved for the HMG-box of a similar mouse protein. [provided by RefSeq, Jul 2008]","start":21592768,"end":21598619,"strand":1,"description":"SRY-box 4 [Source:HGNC Symbol;Acc:HGNC:11200]"}, {"versioned_ensembl_gene_id":"ENSG00000230837.1","gene_symbol":"RPL31P2","gene_name":"ribosomal protein L31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16575]","synonyms":"dJ553F4.5","biotype":"processed_pseudogene","ncbi_id":"140753","summary":null,"start":33752167,"end":33752543,"strand":-1,"description":"ribosomal protein L31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16575]"}, {"versioned_ensembl_gene_id":"ENSG00000229188.2","gene_symbol":"AL050349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33728931,"end":33731828,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127780.3","gene_symbol":"OR1E2","gene_name":"olfactory receptor family 1 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:8190]","synonyms":"OR17-93,OR17-135,OR1E4","biotype":"protein_coding","ncbi_id":"8388","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3432870,"end":3433841,"strand":-1,"description":"olfactory receptor family 1 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:8190]"}, {"versioned_ensembl_gene_id":"ENSG00000186472.19","gene_symbol":"PCLO","gene_name":"piccolo presynaptic cytomatrix protein [Source:HGNC Symbol;Acc:HGNC:13406]","synonyms":"KIAA0559,DKFZp779G1236,ACZ","biotype":"protein_coding","ncbi_id":"27445","summary":"The protein encoded by this gene is part of the presynaptic cytoskeletal matrix, which is involved in establishing active synaptic zones and in synaptic vesicle trafficking. Variations in this gene have been associated with bipolar disorder and major depressive disorder. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":82754013,"end":83162930,"strand":-1,"description":"piccolo presynaptic cytomatrix protein [Source:HGNC Symbol;Acc:HGNC:13406]"}, {"versioned_ensembl_gene_id":"ENSG00000131061.13","gene_symbol":"ZNF341","gene_name":"zinc finger protein 341 [Source:HGNC Symbol;Acc:HGNC:15992]","synonyms":"dJ553F4.3","biotype":"protein_coding","ncbi_id":"84905","summary":null,"start":33731657,"end":33792269,"strand":1,"description":"zinc finger protein 341 [Source:HGNC Symbol;Acc:HGNC:15992]"}, {"versioned_ensembl_gene_id":"ENSG00000233951.3","gene_symbol":"RCC2P3","gene_name":"regulator of chromosome condensation 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42379]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131932","summary":null,"start":138122202,"end":138124595,"strand":1,"description":"regulator of chromosome condensation 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42379]"}, {"versioned_ensembl_gene_id":"ENSG00000250024.1","gene_symbol":"AC122138.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":188990715,"end":189002075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251310.1","gene_symbol":"AC107391.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189193100,"end":189204877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121621.6","gene_symbol":"KIF18A","gene_name":"kinesin family member 18A [Source:HGNC Symbol;Acc:HGNC:29441]","synonyms":"PPP1R99,DKFZP434G2226","biotype":"protein_coding","ncbi_id":"81930","summary":"KIF18A is a member of the kinesin superfamily of microtubule-associated molecular motors (see MIM 148760) that use hydrolysis of ATP to produce force and movement along microtubules (Luboshits and Benayahu, 2005 [PubMed 15878648]).[supplied by OMIM, Aug 2008]","start":28020620,"end":28108308,"strand":-1,"description":"kinesin family member 18A [Source:HGNC Symbol;Acc:HGNC:29441]"}, {"versioned_ensembl_gene_id":"ENSG00000241362.2","gene_symbol":"AC013787.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89687937,"end":89688243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166821.8","gene_symbol":"PEX11A","gene_name":"peroxisomal biogenesis factor 11 alpha [Source:HGNC Symbol;Acc:HGNC:8852]","synonyms":"PEX11-ALPHA,MGC138534,MGC119947","biotype":"protein_coding","ncbi_id":"8800","summary":"This gene is a member of the PEX11 family, which is composed of membrane elongation factors involved in regulation of peroxisome maintenance and proliferation. This gene product interacts with peroxisomal membrane protein 19 and may respond to outside stimuli to increase peroxisome abundance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":89677764,"end":89690783,"strand":-1,"description":"peroxisomal biogenesis factor 11 alpha [Source:HGNC Symbol;Acc:HGNC:8852]"}, {"versioned_ensembl_gene_id":"ENSG00000224093.5","gene_symbol":"AL109613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93592199,"end":93605573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240511.1","gene_symbol":"MED28P2","gene_name":"mediator complex subunit 28 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45079]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480445","summary":null,"start":149099499,"end":149099815,"strand":-1,"description":"mediator complex subunit 28 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45079]"}, {"versioned_ensembl_gene_id":"ENSG00000230439.2","gene_symbol":"AL512488.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93752924,"end":93775444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071794.15","gene_symbol":"HLTF","gene_name":"helicase like transcription factor [Source:HGNC Symbol;Acc:HGNC:11099]","synonyms":"HLTF1,HIP116A,SNF2L3,SMARCA3,RNF80","biotype":"protein_coding","ncbi_id":"6596","summary":"This gene encodes a member of the SWI/SNF family. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein contains a RING finger DNA binding motif. Two transcript variants encoding the same protein have been found for this gene. However, use of an alternative translation start site produces an isoform that is truncated at the N-terminus compared to the full-length protein. [provided by RefSeq, Jul 2008]","start":149030127,"end":149086554,"strand":-1,"description":"helicase like transcription factor [Source:HGNC Symbol;Acc:HGNC:11099]"}, {"versioned_ensembl_gene_id":"ENSG00000166819.11","gene_symbol":"PLIN1","gene_name":"perilipin 1 [Source:HGNC Symbol;Acc:HGNC:9076]","synonyms":"PLIN","biotype":"protein_coding","ncbi_id":"5346","summary":"The protein encoded by this gene coats lipid storage droplets in adipocytes, thereby protecting them until they can be broken down by hormone-sensitive lipase. The encoded protein is the major cAMP-dependent protein kinase substrate in adipocytes and, when unphosphorylated, may play a role in the inhibition of lipolysis. Alternatively spliced transcript variants varying in the 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Feb 2009]","start":89664365,"end":89679427,"strand":-1,"description":"perilipin 1 [Source:HGNC Symbol;Acc:HGNC:9076]"}, {"versioned_ensembl_gene_id":"ENSG00000132879.13","gene_symbol":"FBXO44","gene_name":"F-box protein 44 [Source:HGNC Symbol;Acc:HGNC:24847]","synonyms":"MGC14140,Fbxo6a,Fbx44,FBX30,FBG3","biotype":"protein_coding","ncbi_id":"93611","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. It is also a member of the NFB42 (neural F Box 42 kDa) family, similar to F-box only protein 2 and F-box only protein 6. Several alternatively spliced transcript variants encoding two distinct isoforms have been found for this gene. [provided by RefSeq, Feb 2015]","start":11654375,"end":11663327,"strand":1,"description":"F-box protein 44 [Source:HGNC Symbol;Acc:HGNC:24847]"}, {"versioned_ensembl_gene_id":"ENSG00000267520.2","gene_symbol":"AC010733.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":60925909,"end":60931610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181220.15","gene_symbol":"ZNF746","gene_name":"zinc finger protein 746 [Source:HGNC Symbol;Acc:HGNC:21948]","synonyms":"PARIS,FLJ31413","biotype":"protein_coding","ncbi_id":"155061","summary":null,"start":149472794,"end":149497817,"strand":-1,"description":"zinc finger protein 746 [Source:HGNC Symbol;Acc:HGNC:21948]"}, {"versioned_ensembl_gene_id":"ENSG00000169519.20","gene_symbol":"METTL15","gene_name":"methyltransferase like 15 [Source:HGNC Symbol;Acc:HGNC:26606]","synonyms":"METT5D1,FLJ33979","biotype":"protein_coding","ncbi_id":"196074","summary":null,"start":28108248,"end":28527041,"strand":1,"description":"methyltransferase like 15 [Source:HGNC Symbol;Acc:HGNC:26606]"}, {"versioned_ensembl_gene_id":"ENSG00000276486.1","gene_symbol":"AC022960.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31883288,"end":31883728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276282.1","gene_symbol":"AC022960.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31895745,"end":31896410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257004.1","gene_symbol":"AC008115.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12668982,"end":12685075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263924.1","gene_symbol":"AC022960.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31844388,"end":31845178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263823.1","gene_symbol":"AC009831.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31942575,"end":31944156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183150.7","gene_symbol":"GPR19","gene_name":"G protein-coupled receptor 19 [Source:HGNC Symbol;Acc:HGNC:4473]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2842","summary":null,"start":12660891,"end":12696207,"strand":-1,"description":"G protein-coupled receptor 19 [Source:HGNC Symbol;Acc:HGNC:4473]"}, {"versioned_ensembl_gene_id":"ENSG00000211644.3","gene_symbol":"IGLV1-51","gene_name":"immunoglobulin lambda variable 1-51 [Source:HGNC Symbol;Acc:HGNC:5882]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28820","summary":null,"start":22322472,"end":22322969,"strand":1,"description":"immunoglobulin lambda variable 1-51 [Source:HGNC Symbol;Acc:HGNC:5882]"}, {"versioned_ensembl_gene_id":"ENSG00000211645.2","gene_symbol":"IGLV1-50","gene_name":"immunoglobulin lambda variable 1-50 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5881]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28821","summary":null,"start":22327300,"end":22327814,"strand":1,"description":"immunoglobulin lambda variable 1-50 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5881]"}, {"versioned_ensembl_gene_id":"ENSG00000136542.8","gene_symbol":"GALNT5","gene_name":"polypeptide N-acetylgalactosaminyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4127]","synonyms":"GalNAc-T5","biotype":"protein_coding","ncbi_id":"11227","summary":"The protein encoded by this gene is a membrane-bound polypeptide N-acetylgalactosaminyltransferase that is found in the Golgi. The encoded protein catalyzes the first step in the mucin-type O-glycosylation of Golgi proteins, transfering an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. [provided by RefSeq, Aug 2016]","start":157257598,"end":157314211,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4127]"}, {"versioned_ensembl_gene_id":"ENSG00000225724.1","gene_symbol":"ASH2LP3","gene_name":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:53060]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100736411","summary":null,"start":22339573,"end":22341214,"strand":1,"description":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:53060]"}, {"versioned_ensembl_gene_id":"ENSG00000223350.2","gene_symbol":"IGLV9-49","gene_name":"immunoglobulin lambda variable 9-49 [Source:HGNC Symbol;Acc:HGNC:5933]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28773","summary":null,"start":22343187,"end":22343732,"strand":1,"description":"immunoglobulin lambda variable 9-49 [Source:HGNC Symbol;Acc:HGNC:5933]"}, {"versioned_ensembl_gene_id":"ENSG00000232515.1","gene_symbol":"AC245060.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22347807,"end":22348164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249030.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29413850,"end":29414796,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000211647.1","gene_symbol":"IGLV5-48","gene_name":"immunoglobulin lambda variable 5-48 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5925]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28780","summary":null,"start":22352940,"end":22353433,"strand":1,"description":"immunoglobulin lambda variable 5-48 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5925]"}, {"versioned_ensembl_gene_id":"ENSG00000235966.4","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"protein_coding","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29393135,"end":29394203,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000211648.2","gene_symbol":"IGLV1-47","gene_name":"immunoglobulin lambda variable 1-47 [Source:HGNC Symbol;Acc:HGNC:5880]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28822","summary":null,"start":22357739,"end":22358260,"strand":1,"description":"immunoglobulin lambda variable 1-47 [Source:HGNC Symbol;Acc:HGNC:5880]"}, {"versioned_ensembl_gene_id":"ENSG00000239985.2","gene_symbol":"AC073210.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65038372,"end":65038565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251394.6","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29370147,"end":29446668,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000198547.8","gene_symbol":"C20orf203","gene_name":"chromosome 20 open reading frame 203 [Source:HGNC Symbol;Acc:HGNC:26592]","synonyms":"FLJ33706","biotype":"lincRNA","ncbi_id":"284805","summary":"The protein encoded by this gene is thought to be a human-specific protein. Currently available evidence suggests that orthologous regions in other organisms contain sequence differences that would not support production of a protein product. Genome-wide association studies have suggested the possibility that a SNP in the 3' UTR, rs17123507, could be associated with nicotine addiction. Expression of this gene may be elevated in some individuals with Alzheimer's disease. [provided by RefSeq, Mar 2017]","start":32631652,"end":32673941,"strand":-1,"description":"chromosome 20 open reading frame 203 [Source:HGNC Symbol;Acc:HGNC:26592]"}, {"versioned_ensembl_gene_id":"ENSG00000237428.1","gene_symbol":"ASH2LP2","gene_name":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:53059]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422088","summary":null,"start":22366210,"end":22367770,"strand":1,"description":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:53059]"}, {"versioned_ensembl_gene_id":"ENSG00000211649.3","gene_symbol":"IGLV7-46","gene_name":"immunoglobulin lambda variable 7-46 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5930]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28775","summary":null,"start":22369614,"end":22370087,"strand":1,"description":"immunoglobulin lambda variable 7-46 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5930]"}, {"versioned_ensembl_gene_id":"ENSG00000224234.5","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29435874,"end":29437545,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000166803.11","gene_symbol":"PCLAF","gene_name":"PCNA clamp associated factor [Source:HGNC Symbol;Acc:HGNC:28961]","synonyms":"PAF15,p15(PAF),OEATC-1,NS5ATP9,KIAA0101","biotype":"protein_coding","ncbi_id":"9768","summary":null,"start":64364311,"end":64387687,"strand":-1,"description":"PCNA clamp associated factor [Source:HGNC Symbol;Acc:HGNC:28961]"}, {"versioned_ensembl_gene_id":"ENSG00000230780.8","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"hs6M1-18,OR11A2","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29422072,"end":29453643,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000260480.1","gene_symbol":"C2orf69P4","gene_name":"chromosome 2 open reading frame 69 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420859","summary":null,"start":35352482,"end":35353022,"strand":1,"description":"chromosome 2 open reading frame 69 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51803]"}, {"versioned_ensembl_gene_id":"ENSG00000229414.2","gene_symbol":"KCNQ1-AS1","gene_name":"KCNQ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42790]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338653","summary":null,"start":2840135,"end":2861568,"strand":-1,"description":"KCNQ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42790]"}, {"versioned_ensembl_gene_id":"ENSG00000225979.1","gene_symbol":"AC010746.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197311393,"end":197312740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232603.1","gene_symbol":"AC245291.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22370829,"end":22371120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259841.6","gene_symbol":"LINC01566","gene_name":"long intergenic non-protein coding RNA 1566 [Source:HGNC Symbol;Acc:HGNC:27555]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283914","summary":null,"start":35363412,"end":35390584,"strand":1,"description":"long intergenic non-protein coding RNA 1566 [Source:HGNC Symbol;Acc:HGNC:27555]"}, {"versioned_ensembl_gene_id":"ENSG00000131871.14","gene_symbol":"SELENOS","gene_name":"selenoprotein S [Source:HGNC Symbol;Acc:HGNC:30396]","synonyms":"VIMP,SEPS1,SELS,SBBI8,MGC2553,AD-015","biotype":"protein_coding","ncbi_id":"55829","summary":"This gene encodes a transmembrane protein that is localized in the endoplasmic reticulum (ER). It is involved in the degradation process of misfolded proteins in the ER, and may also have a role in inflammation control. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Two additional phylogenetically conserved stem-loop structures (Stem-loop 1 and Stem-loop 2) in the 3' UTR of this mRNA have been shown to function as modulators of Sec insertion. An alternatively spliced transcript variant, lacking the SECIS element and encoding a non-Sec containing shorter isoform, has been described for this gene (PMID:23614019). [provided by RefSeq, Jul 2017]","start":101270817,"end":101277500,"strand":-1,"description":"selenoprotein S [Source:HGNC Symbol;Acc:HGNC:30396]"}, {"versioned_ensembl_gene_id":"ENSG00000211650.2","gene_symbol":"IGLV5-45","gene_name":"immunoglobulin lambda variable 5-45 [Source:HGNC Symbol;Acc:HGNC:5924]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28781","summary":null,"start":22375986,"end":22376505,"strand":1,"description":"immunoglobulin lambda variable 5-45 [Source:HGNC Symbol;Acc:HGNC:5924]"}, {"versioned_ensembl_gene_id":"ENSG00000130332.14","gene_symbol":"LSM7","gene_name":"LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:20470]","synonyms":"YNL147W","biotype":"protein_coding","ncbi_id":"51690","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]","start":2321517,"end":2328620,"strand":-1,"description":"LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:20470]"}, {"versioned_ensembl_gene_id":"ENSG00000277190.1","gene_symbol":"AC010492.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54225142,"end":54225500,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233046.8","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29351939,"end":29428535,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000260291.1","gene_symbol":"FRG2GP","gene_name":"FSHD region gene 2 family member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:51364]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480321","summary":null,"start":35384144,"end":35385086,"strand":-1,"description":"FSHD region gene 2 family member G, pseudogene [Source:HGNC Symbol;Acc:HGNC:51364]"}, {"versioned_ensembl_gene_id":"ENSG00000227296.4","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29879033,"end":29881754,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000220517.2","gene_symbol":"ASS1P1","gene_name":"argininosuccinate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:759]","synonyms":"ASSP1","biotype":"processed_pseudogene","ncbi_id":"442167","summary":null,"start":25023247,"end":25024483,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:759]"}, {"versioned_ensembl_gene_id":"ENSG00000232362.1","gene_symbol":"ATP5LP2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13215]","synonyms":"ATP5KP2","biotype":"processed_pseudogene","ncbi_id":"53410","summary":null,"start":122859678,"end":122859988,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13215]"}, {"versioned_ensembl_gene_id":"ENSG00000272936.1","gene_symbol":"AC096586.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44704405,"end":44704965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231429.2","gene_symbol":"AC244021.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121412719,"end":121429274,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101916.11","gene_symbol":"TLR8","gene_name":"toll like receptor 8 [Source:HGNC Symbol;Acc:HGNC:15632]","synonyms":"CD288","biotype":"protein_coding","ncbi_id":"51311","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is predominantly expressed in lung and peripheral blood leukocytes, and lies in close proximity to another family member, TLR7, on chromosome X. [provided by RefSeq, Jul 2008]","start":12906620,"end":12923169,"strand":1,"description":"toll like receptor 8 [Source:HGNC Symbol;Acc:HGNC:15632]"}, {"versioned_ensembl_gene_id":"ENSG00000119714.10","gene_symbol":"GPR68","gene_name":"G protein-coupled receptor 68 [Source:HGNC Symbol;Acc:HGNC:4519]","synonyms":"OGR1","biotype":"protein_coding","ncbi_id":"8111","summary":"The protein encoded by this gene is a G protein-coupled receptor for sphingosylphosphorylcholine. The encoded protein is a proton-sensing receptor, inactive at pH 7.8 but active at pH 6.8. Mutations in this gene are a cause of amelogenesis imperfecta. [provided by RefSeq, Feb 2017]","start":91232532,"end":91253925,"strand":-1,"description":"G protein-coupled receptor 68 [Source:HGNC Symbol;Acc:HGNC:4519]"}, {"versioned_ensembl_gene_id":"ENSG00000165762.3","gene_symbol":"OR4K2","gene_name":"olfactory receptor family 4 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14728]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390431","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":19875142,"end":19883932,"strand":1,"description":"olfactory receptor family 4 subfamily K member 2 [Source:HGNC Symbol;Acc:HGNC:14728]"}, {"versioned_ensembl_gene_id":"ENSG00000137822.12","gene_symbol":"TUBGCP4","gene_name":"tubulin gamma complex associated protein 4 [Source:HGNC Symbol;Acc:HGNC:16691]","synonyms":"FLJ14797,76P","biotype":"protein_coding","ncbi_id":"27229","summary":"This gene encodes a component of the gamma-tubulin ring complex, which is required for microtubule nucleation. In mammalian cells, the protein localizes to centrosomes in association with gamma-tubulin. Crystal structure analysis revealed a structure composed of five helical bundles arranged around conserved hydrophobic cores. An exposed surface area located in the C-terminal domain is essential and sufficient for direct binding to gamma-tubulin. Mutations in this gene that alter microtubule organization are associated with microcephaly and chorioretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015]","start":43369221,"end":43409771,"strand":1,"description":"tubulin gamma complex associated protein 4 [Source:HGNC Symbol;Acc:HGNC:16691]"}, {"versioned_ensembl_gene_id":"ENSG00000178718.6","gene_symbol":"RPP25","gene_name":"ribonuclease P and MRP subunit p25 [Source:HGNC Symbol;Acc:HGNC:30361]","synonyms":"FLJ20374","biotype":"protein_coding","ncbi_id":"54913","summary":null,"start":74954416,"end":74957464,"strand":-1,"description":"ribonuclease P and MRP subunit p25 [Source:HGNC Symbol;Acc:HGNC:30361]"}, {"versioned_ensembl_gene_id":"ENSG00000068976.13","gene_symbol":"PYGM","gene_name":"glycogen phosphorylase, muscle associated [Source:HGNC Symbol;Acc:HGNC:9726]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5837","summary":"This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]","start":64746389,"end":64760297,"strand":-1,"description":"glycogen phosphorylase, muscle associated [Source:HGNC Symbol;Acc:HGNC:9726]"}, {"versioned_ensembl_gene_id":"ENSG00000176105.13","gene_symbol":"YES1","gene_name":"YES proto-oncogene 1, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12841]","synonyms":"Yes,HsT441,c-yes","biotype":"protein_coding","ncbi_id":"7525","summary":"This gene is the cellular homolog of the Yamaguchi sarcoma virus oncogene. The encoded protein has tyrosine kinase activity and belongs to the src family of proteins. This gene lies in close proximity to thymidylate synthase gene on chromosome 18, and a corresponding pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008]","start":721588,"end":812546,"strand":-1,"description":"YES proto-oncogene 1, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12841]"}, {"versioned_ensembl_gene_id":"ENSG00000255572.1","gene_symbol":"AC018653.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7166674,"end":7189069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270709.1","gene_symbol":"AL109653.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145768095,"end":145768342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236045.1","gene_symbol":"AL031283.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15334166,"end":15335464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142621.19","gene_symbol":"FHAD1","gene_name":"forkhead associated phosphopeptide binding domain 1 [Source:HGNC Symbol;Acc:HGNC:29408]","synonyms":"KIAA1937","biotype":"protein_coding","ncbi_id":"114827","summary":null,"start":15247272,"end":15400283,"strand":1,"description":"forkhead associated phosphopeptide binding domain 1 [Source:HGNC Symbol;Acc:HGNC:29408]"}, {"versioned_ensembl_gene_id":"ENSG00000272923.1","gene_symbol":"AC092139.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81385463,"end":81387560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174990.4","gene_symbol":"CA5A","gene_name":"carbonic anhydrase 5A [Source:HGNC Symbol;Acc:HGNC:1377]","synonyms":"CAVA,CAV,CA5","biotype":"protein_coding","ncbi_id":"763","summary":" Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA VA is localized in the mitochondria and expressed primarily in the liver. It may play an important role in ureagenesis and gluconeogenesis. CA5A gene maps to chromosome 16q24.3 and an unprocessed pseudogene has been assigned to 16p12-p11.2. [provided by RefSeq, Jul 2008]","start":87881546,"end":87936529,"strand":-1,"description":"carbonic anhydrase 5A [Source:HGNC Symbol;Acc:HGNC:1377]"}, {"versioned_ensembl_gene_id":"ENSG00000278857.1","gene_symbol":"IGKV1D-12","gene_name":"immunoglobulin kappa variable 1D-12 [Source:HGNC Symbol;Acc:HGNC:5746]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28903","summary":null,"start":90159840,"end":90160335,"strand":1,"description":"immunoglobulin kappa variable 1D-12 [Source:HGNC Symbol;Acc:HGNC:5746]"}, {"versioned_ensembl_gene_id":"ENSG00000270385.1","gene_symbol":"AC133539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87892955,"end":87893735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139722.6","gene_symbol":"VPS37B","gene_name":"VPS37B, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:25754]","synonyms":"FLJ12750","biotype":"protein_coding","ncbi_id":"79720","summary":null,"start":122865328,"end":122896444,"strand":-1,"description":"VPS37B, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:25754]"}, {"versioned_ensembl_gene_id":"ENSG00000258133.1","gene_symbol":"AC025578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58394596,"end":58395138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107201.9","gene_symbol":"DDX58","gene_name":"DExD/H-box helicase 58 [Source:HGNC Symbol;Acc:HGNC:19102]","synonyms":"RIG-I,FLJ13599,DKFZp434J1111","biotype":"protein_coding","ncbi_id":"23586","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases which are implicated in a number of cellular processes involving RNA binding and alteration of RNA secondary structure. This gene encodes a protein containing RNA helicase-DEAD box protein motifs and a caspase recruitment domain (CARD). It is involved in viral double-stranded (ds) RNA recognition and the regulation of the antiviral innate immune response. Mutations in this gene are associated with Singleton-Merten syndrome 2. [provided by RefSeq, Aug 2020]","start":32455705,"end":32526324,"strand":-1,"description":"DExD/H-box helicase 58 [Source:HGNC Symbol;Acc:HGNC:19102]"}, {"versioned_ensembl_gene_id":"ENSG00000225060.8","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30754873,"end":30766379,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000279411.1","gene_symbol":"AC090643.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58103907,"end":58105935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279134.1","gene_symbol":"AC090643.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":58094914,"end":58098013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170920.2","gene_symbol":"OR7G3","gene_name":"olfactory receptor family 7 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:8467]","synonyms":"OST085","biotype":"protein_coding","ncbi_id":"390883","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9126012,"end":9126950,"strand":-1,"description":"olfactory receptor family 7 subfamily G member 3 [Source:HGNC Symbol;Acc:HGNC:8467]"}, {"versioned_ensembl_gene_id":"ENSG00000263279.1","gene_symbol":"AC007595.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10691273,"end":10692973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249565.2","gene_symbol":"SERBP1P5","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44632]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442112","summary":null,"start":78180866,"end":78182046,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44632]"}, {"versioned_ensembl_gene_id":"ENSG00000239335.4","gene_symbol":"LLPH-AS1","gene_name":"LLPH antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50493]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103625681","summary":null,"start":66130751,"end":66134449,"strand":1,"description":"LLPH antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50493]"}, {"versioned_ensembl_gene_id":"ENSG00000251535.1","gene_symbol":"AC079140.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":336258,"end":336786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283633.1","gene_symbol":"AP000547.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16601911,"end":16615111,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241717.1","gene_symbol":"VWFP1","gene_name":"von Willebrand factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12727]","synonyms":"VWFP,F8VWFP,F8VWFL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"7451","summary":null,"start":16690103,"end":16704477,"strand":-1,"description":"von Willebrand factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12727]"}, {"versioned_ensembl_gene_id":"ENSG00000260205.1","gene_symbol":"AL157831.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22218074,"end":22221168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249288.1","gene_symbol":"SLC25A15P5","gene_name":"solute carrier family 25 member 15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39846]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422642","summary":null,"start":16645695,"end":16646581,"strand":-1,"description":"solute carrier family 25 member 15 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39846]"}, {"versioned_ensembl_gene_id":"ENSG00000064309.14","gene_symbol":"CDON","gene_name":"cell adhesion associated, oncogene regulated [Source:HGNC Symbol;Acc:HGNC:17104]","synonyms":"ORCAM,CDON1,CDO","biotype":"protein_coding","ncbi_id":"50937","summary":"This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and positively regulates myogenesis. [provided by RefSeq, Aug 2011]","start":125955796,"end":126063335,"strand":-1,"description":"cell adhesion associated, oncogene regulated [Source:HGNC Symbol;Acc:HGNC:17104]"}, {"versioned_ensembl_gene_id":"ENSG00000272333.5","gene_symbol":"KMT2B","gene_name":"lysine methyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:15840]","synonyms":"WBP7,TRX2,MLL4,MLL2,MLL1B,KIAA0304,HRX2,CXXC10","biotype":"protein_coding","ncbi_id":"9757","summary":"This gene encodes a protein which contains multiple domains including a CXXC zinc finger, three PHD zinc fingers, two FY-rich domains, and a SET (suppressor of variegation, enhancer of zeste, and trithorax) domain. The SET domain is a conserved C-terminal domain that characterizes proteins of the MLL (mixed-lineage leukemia) family. This gene is ubiquitously expressed in adult tissues. It is also amplified in solid tumor cell lines, and may be involved in human cancer. Two alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene, however, the full length nature of the shorter transcript is not known. [provided by RefSeq, Jul 2008]","start":35718019,"end":35738878,"strand":1,"description":"lysine methyltransferase 2B [Source:HGNC Symbol;Acc:HGNC:15840]"}, {"versioned_ensembl_gene_id":"ENSG00000283703.1","gene_symbol":"VSIG10L2","gene_name":"V-set and immunoglobulin domain containing 10 like 2 [Source:HGNC Symbol;Acc:HGNC:27879]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338667","summary":null,"start":125946056,"end":125956319,"strand":1,"description":"V-set and immunoglobulin domain containing 10 like 2 [Source:HGNC Symbol;Acc:HGNC:27879]"}, {"versioned_ensembl_gene_id":"ENSG00000184347.14","gene_symbol":"SLIT3","gene_name":"slit guidance ligand 3 [Source:HGNC Symbol;Acc:HGNC:11087]","synonyms":"slit2,SLIT1,Slit-3,SLIL2,MEGF5","biotype":"protein_coding","ncbi_id":"6586","summary":"The protein encoded by this gene is secreted, likely interacting with roundabout homolog receptors to effect cell migration. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]","start":168661733,"end":169301129,"strand":-1,"description":"slit guidance ligand 3 [Source:HGNC Symbol;Acc:HGNC:11087]"}, {"versioned_ensembl_gene_id":"ENSG00000220447.1","gene_symbol":"AL139098.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121381472,"end":121381860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183395.4","gene_symbol":"PMCH","gene_name":"pro-melanin concentrating hormone [Source:HGNC Symbol;Acc:HGNC:9109]","synonyms":"MCH","biotype":"protein_coding","ncbi_id":"5367","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include melanin-concentrating hormone (MCH), neuropeptide-glutamic acid-isoleucine (NEI), and neuropeptide-glycine-glutamic acid (NGE). Melanin-concentrating hormone is a 19-amino acid neuropeptide that stimulates hunger and may additionally regulate energy homeostasis, reproductive function, and sleep. Pseudogenes of this gene have been identified on chromosome 5. [provided by RefSeq, Jul 2015]","start":102196459,"end":102197845,"strand":-1,"description":"pro-melanin concentrating hormone [Source:HGNC Symbol;Acc:HGNC:9109]"}, {"versioned_ensembl_gene_id":"ENSG00000223487.1","gene_symbol":"FRMPD4-AS1","gene_name":"FRMPD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41222]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874121","summary":null,"start":12373167,"end":12375133,"strand":-1,"description":"FRMPD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41222]"}, {"versioned_ensembl_gene_id":"ENSG00000258142.2","gene_symbol":"AC093023.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102230027,"end":102230533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154316.16","gene_symbol":"TDH","gene_name":"L-threonine dehydrogenase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15547]","synonyms":"SDR14E1P,FLJ25033","biotype":"transcribed_unitary_pseudogene","ncbi_id":"157739","summary":"This gene appears to be an evolving pseudogene of L-threonine 3-dehydrogenase (TDH). In both prokaryotes and eukaryotes, TDH catalyzes the first of two steps in one of two L-threonine degradation pathways. However, in human, the single gene with sequence similarity to TDH is not capable of encoding a functional TDH protein; the predicted protein lacks most of the C-terminus and parts of the NAD+ binding motif when compared to other species' TDH proteins. This suggests that the human gene is therefore a pseudogene. Transcripts of this gene are found in all tissues and alternatively spliced transcripts have been described. It is not known if these transcripts are translated, or if the possible protein product provides any functional role. [provided by RefSeq, Jul 2008]","start":11339637,"end":11368452,"strand":1,"description":"L-threonine dehydrogenase (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15547]"}, {"versioned_ensembl_gene_id":"ENSG00000213996.12","gene_symbol":"TM6SF2","gene_name":"transmembrane 6 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11861]","synonyms":"Lpr4","biotype":"protein_coding","ncbi_id":"53345","summary":null,"start":19264364,"end":19273391,"strand":-1,"description":"transmembrane 6 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11861]"}, {"versioned_ensembl_gene_id":"ENSG00000267298.1","gene_symbol":"AC006116.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56311928,"end":56312486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279479.1","gene_symbol":"AP005205.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6727053,"end":6728981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266907.1","gene_symbol":"AC006116.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56319790,"end":56322310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241560.5","gene_symbol":"ZBTB20-AS1","gene_name":"ZBTB20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40640]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131117","summary":null,"start":114351811,"end":114388978,"strand":1,"description":"ZBTB20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40640]"}, {"versioned_ensembl_gene_id":"ENSG00000126822.16","gene_symbol":"PLEKHG3","gene_name":"pleckstrin homology and RhoGEF domain containing G3 [Source:HGNC Symbol;Acc:HGNC:20364]","synonyms":"KIAA0599,ARHGEF43","biotype":"protein_coding","ncbi_id":"26030","summary":null,"start":64704102,"end":64750247,"strand":1,"description":"pleckstrin homology and RhoGEF domain containing G3 [Source:HGNC Symbol;Acc:HGNC:20364]"}, {"versioned_ensembl_gene_id":"ENSG00000256259.1","gene_symbol":"LINC02425","gene_name":"long intergenic non-protein coding RNA 2425 [Source:HGNC Symbol;Acc:HGNC:53356]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369810","summary":null,"start":66027725,"end":66031066,"strand":-1,"description":"long intergenic non-protein coding RNA 2425 [Source:HGNC Symbol;Acc:HGNC:53356]"}, {"versioned_ensembl_gene_id":"ENSG00000278644.2","gene_symbol":"PCGF2","gene_name":"polycomb group ring finger 2 [Source:HGNC Symbol;Acc:HGNC:12929]","synonyms":"ZNF144,RNF110,MEL-18","biotype":"protein_coding","ncbi_id":"7703","summary":"The protein encoded by this gene contains a RING finger motif and is similar to the polycomb group (PcG) gene products. PcG gene products form complexes via protein-protein interaction and maintain the transcription repression of genes involved in embryogenesis, cell cycles, and tumorigenesis. This protein was shown to act as a negative regulator of transcription and has tumor suppressor activity. The expression of this gene was detected in various tumor cells, but is limited in neural organs in normal tissues. Knockout studies in mice suggested that this protein may negatively regulate the expression of different cytokines, chemokines, and chemokine receptors, and thus plays an important role in lymphocyte differentiation and migration, as well as in immune responses. [provided by RefSeq, Jul 2008]","start":38534684,"end":38550604,"strand":-1,"description":"polycomb group ring finger 2 [Source:HGNC Symbol;Acc:HGNC:12929]"}, {"versioned_ensembl_gene_id":"ENSG00000232875.1","gene_symbol":"HMGN2P35","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874479","summary":null,"start":96915633,"end":96915902,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:39406]"}, {"versioned_ensembl_gene_id":"ENSG00000276306.1","gene_symbol":"AC245128.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044524.10","gene_symbol":"EPHA3","gene_name":"EPH receptor A3 [Source:HGNC Symbol;Acc:HGNC:3387]","synonyms":"TYRO4,HEK4,HEK,ETK1,ETK","biotype":"protein_coding","ncbi_id":"2042","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Two alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jul 2008]","start":89107524,"end":89482134,"strand":1,"description":"EPH receptor A3 [Source:HGNC Symbol;Acc:HGNC:3387]"}, {"versioned_ensembl_gene_id":"ENSG00000112493.12","gene_symbol":"TAPBP","gene_name":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]","synonyms":"TAPA","biotype":"protein_coding","ncbi_id":"6892","summary":"This gene encodes a transmembrane glycoprotein which mediates interaction between newly assembled major histocompatibility complex (MHC) class I molecules and the transporter associated with antigen processing (TAP), which is required for the transport of antigenic peptides across the endoplasmic reticulum membrane. This interaction is essential for optimal peptide loading on the MHC class I molecule. Up to four complexes of MHC class I and this protein may be bound to a single TAP molecule. This protein contains a C-terminal double-lysine motif (KKKAE) known to maintain membrane proteins in the endoplasmic reticulum. This gene lies within the major histocompatibility complex on chromosome 6. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":33221298,"end":33235989,"strand":-1,"description":"TAP binding protein [Source:HGNC Symbol;Acc:HGNC:11566]"}, {"versioned_ensembl_gene_id":"ENSG00000100505.13","gene_symbol":"TRIM9","gene_name":"tripartite motif containing 9 [Source:HGNC Symbol;Acc:HGNC:16288]","synonyms":"SPRING,RNF91","biotype":"protein_coding","ncbi_id":"114088","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Its function has not been identified. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":50975262,"end":51096061,"strand":-1,"description":"tripartite motif containing 9 [Source:HGNC Symbol;Acc:HGNC:16288]"}, {"versioned_ensembl_gene_id":"ENSG00000223595.1","gene_symbol":"LYPLA1P1","gene_name":"lysophospholipase I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129401","summary":null,"start":123230120,"end":123230741,"strand":-1,"description":"lysophospholipase I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44005]"}, {"versioned_ensembl_gene_id":"ENSG00000179362.14","gene_symbol":"HMGN2P46","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:26817]","synonyms":"FLJ39426,D-PCa-2,C15orf21","biotype":"transcribed_processed_pseudogene","ncbi_id":"283651","summary":null,"start":45511136,"end":45586290,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:26817]"}, {"versioned_ensembl_gene_id":"ENSG00000198104.3","gene_symbol":"OR2T6","gene_name":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]","synonyms":"OR2T9,OR2T6P,OST703","biotype":"protein_coding","ncbi_id":"254879","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248375746,"end":248391811,"strand":1,"description":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]"}, {"versioned_ensembl_gene_id":"ENSG00000112312.9","gene_symbol":"GMNN","gene_name":"geminin, DNA replication inhibitor [Source:HGNC Symbol;Acc:HGNC:17493]","synonyms":"Gem","biotype":"protein_coding","ncbi_id":"51053","summary":"This gene encodes a protein that plays a critical role in cell cycle regulation. The encoded protein inhibits DNA replication by binding to DNA replication factor Cdt1, preventing the incorporation of minichromosome maintenance proteins into the pre-replication complex. The encoded protein is expressed during the S and G2 phases of the cell cycle and is degraded by the anaphase-promoting complex during the metaphase-anaphase transition. Increased expression of this gene may play a role in several malignancies including colon, rectal and breast cancer. Alternatively spliced transcript variants have been observed for this gene, and two pseudogenes of this gene are located on the short arm of chromosome 16. [provided by RefSeq, Oct 2011]","start":24774931,"end":24786099,"strand":1,"description":"geminin, DNA replication inhibitor [Source:HGNC Symbol;Acc:HGNC:17493]"}, {"versioned_ensembl_gene_id":"ENSG00000279794.1","gene_symbol":"AC024580.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56149817,"end":56150490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234261.3","gene_symbol":"AL138720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14661829,"end":15090003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260519.1","gene_symbol":"AC096734.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42657496,"end":42657928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170312.15","gene_symbol":"CDK1","gene_name":"cyclin dependent kinase 1 [Source:HGNC Symbol;Acc:HGNC:1722]","synonyms":"CDC28A,CDC2","biotype":"protein_coding","ncbi_id":"983","summary":"The protein encoded by this gene is a member of the Ser/Thr protein kinase family. This protein is a catalytic subunit of the highly conserved protein kinase complex known as M-phase promoting factor (MPF), which is essential for G1/S and G2/M phase transitions of eukaryotic cell cycle. Mitotic cyclins stably associate with this protein and function as regulatory subunits. The kinase activity of this protein is controlled by cyclin accumulation and destruction through the cell cycle. The phosphorylation and dephosphorylation of this protein also play important regulatory roles in cell cycle control. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":60778331,"end":60794852,"strand":1,"description":"cyclin dependent kinase 1 [Source:HGNC Symbol;Acc:HGNC:1722]"}, {"versioned_ensembl_gene_id":"ENSG00000131080.14","gene_symbol":"EDA2R","gene_name":"ectodysplasin A2 receptor [Source:HGNC Symbol;Acc:HGNC:17756]","synonyms":"XEDAR,TNFRSF27,EDAA2R,EDA-A2R","biotype":"protein_coding","ncbi_id":"60401","summary":"The protein encoded by this gene is a type III transmembrane protein of the TNFR (tumor necrosis factor receptor) superfamily, and contains cysteine-rich repeats and a single transmembrane domain. This protein binds to the EDA-A2 isoform of ectodysplasin, which plays an important role in maintenance of hair and teeth. Alternatively spliced transcript variants encodes distinct protein isoforms. [provided by RefSeq, Apr 2016]","start":66595637,"end":66639298,"strand":-1,"description":"ectodysplasin A2 receptor [Source:HGNC Symbol;Acc:HGNC:17756]"}, {"versioned_ensembl_gene_id":"ENSG00000273594.4","gene_symbol":"EEF1D","gene_name":"eukaryotic translation elongation factor 1 delta [Source:HGNC Symbol;Acc:HGNC:3211]","synonyms":"FLJ20897,EF-1D","biotype":"protein_coding","ncbi_id":"1936","summary":"This gene encodes a subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This subunit, delta, functions as guanine nucleotide exchange factor. It is reported that following HIV-1 infection, this subunit interacts with HIV-1 Tat. This interaction results in repression of translation of host cell proteins and enhanced translation of viral proteins. Several alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. Related pseudogenes have been defined on chromosomes 1, 6, 7, 9, 11, 13, 17, 19.[provided by RefSeq, Aug 2010]","start":143579697,"end":143597744,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta [Source:HGNC Symbol;Acc:HGNC:3211]"}, {"versioned_ensembl_gene_id":"ENSG00000279583.1","gene_symbol":"AC009086.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29595130,"end":29596137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120694.19","gene_symbol":"HSPH1","gene_name":"heat shock protein family H (Hsp110) member 1 [Source:HGNC Symbol;Acc:HGNC:16969]","synonyms":"NY-CO-25,KIAA0201,HSP105B,HSP105A","biotype":"protein_coding","ncbi_id":"10808","summary":"This gene encodes a member of the heat shock protein 70 family of proteins. The encoded protein functions as a nucleotide exchange factor for the molecular chaperone heat shock cognate 71 kDa protein (Hsc70). In addition, this protein plays a distinct but related role as a holdase that inhibits the aggregation of misfolded proteins, including the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Elevated expression of this protein has been observed in numerous human cancers. [provided by RefSeq, Mar 2017]","start":31134974,"end":31162388,"strand":-1,"description":"heat shock protein family H (Hsp110) member 1 [Source:HGNC Symbol;Acc:HGNC:16969]"}, {"versioned_ensembl_gene_id":"ENSG00000135472.8","gene_symbol":"FAIM2","gene_name":"Fas apoptotic inhibitory molecule 2 [Source:HGNC Symbol;Acc:HGNC:17067]","synonyms":"TMBIM2,NMP35,LIFEGUARD,LFG2,LFG,KIAA0950","biotype":"protein_coding","ncbi_id":"23017","summary":null,"start":49866896,"end":49904217,"strand":-1,"description":"Fas apoptotic inhibitory molecule 2 [Source:HGNC Symbol;Acc:HGNC:17067]"}, {"versioned_ensembl_gene_id":"ENSG00000267317.2","gene_symbol":"AC027307.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1457670,"end":1458580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281971.1","gene_symbol":"HOMER2P1","gene_name":"homer scaffolding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20336]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"317768","summary":null,"start":106484773,"end":106485736,"strand":-1,"description":"homer scaffolding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20336]"}, {"versioned_ensembl_gene_id":"ENSG00000263707.1","gene_symbol":"AC005277.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12990149,"end":12990610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267052.1","gene_symbol":"AC005050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106570947,"end":106598908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177710.5","gene_symbol":"SLC35G5","gene_name":"solute carrier family 35 member G5 [Source:HGNC Symbol;Acc:HGNC:15546]","synonyms":"AMAC1L2,AMAC","biotype":"protein_coding","ncbi_id":"83650","summary":"This gene is intronless and probably arose from retrotransposition of a similar gene. It has high sequence similarity to the gene encoding acyl-malonyl condensing enzyme on chromosome 17. [provided by RefSeq, Aug 2011]","start":11330888,"end":11332208,"strand":1,"description":"solute carrier family 35 member G5 [Source:HGNC Symbol;Acc:HGNC:15546]"}, {"versioned_ensembl_gene_id":"ENSG00000178537.9","gene_symbol":"SLC25A20","gene_name":"solute carrier family 25 member 20 [Source:HGNC Symbol;Acc:HGNC:1421]","synonyms":"CACT,CAC","biotype":"protein_coding","ncbi_id":"788","summary":"This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq, Jul 2008]","start":48856931,"end":48898993,"strand":-1,"description":"solute carrier family 25 member 20 [Source:HGNC Symbol;Acc:HGNC:1421]"}, {"versioned_ensembl_gene_id":"ENSG00000204791.9","gene_symbol":"SMPD5","gene_name":"sphingomyelin phosphodiesterase 5 [Source:HGNC Symbol;Acc:HGNC:52275]","synonyms":"MA-nSMase","biotype":"transcribed_unitary_pseudogene","ncbi_id":"392275","summary":null,"start":144049079,"end":144051522,"strand":1,"description":"sphingomyelin phosphodiesterase 5 [Source:HGNC Symbol;Acc:HGNC:52275]"}, {"versioned_ensembl_gene_id":"ENSG00000205755.11","gene_symbol":"CRLF2","gene_name":"cytokine receptor like factor 2 [Source:HGNC Symbol;Acc:HGNC:14281]","synonyms":"TSLPR,CRL2","biotype":"protein_coding","ncbi_id":"64109","summary":"This gene encodes a member of the type I cytokine receptor family. The encoded protein is a receptor for thymic stromal lymphopoietin (TSLP). Together with the interleukin 7 receptor (IL7R), the encoded protein and TSLP activate STAT3, STAT5, and JAK2 pathways, which control processes such as cell proliferation and development of the hematopoietic system. Rearrangement of this gene with immunoglobulin heavy chain gene (IGH) on chromosome 14, or with P2Y purinoceptor 8 gene (P2RY8) on the same X or Y chromosomes is associated with B-progenitor acute lymphoblastic leukemia (ALL) and Down syndrome ALL. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":1187549,"end":1212750,"strand":-1,"description":"cytokine receptor like factor 2 [Source:HGNC Symbol;Acc:HGNC:14281]"}, {"versioned_ensembl_gene_id":"ENSG00000281082.1","gene_symbol":"AC131097.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":241800916,"end":241801907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279263.1","gene_symbol":"OR2L8","gene_name":"olfactory receptor family 2 subfamily L member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15014]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"391190","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":247948858,"end":247949796,"strand":1,"description":"olfactory receptor family 2 subfamily L member 8 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15014]"}, {"versioned_ensembl_gene_id":"ENSG00000226191.3","gene_symbol":"CLK3P2","gene_name":"CDC like kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49786]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128834","summary":null,"start":247936061,"end":247937513,"strand":-1,"description":"CDC like kinase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49786]"}, {"versioned_ensembl_gene_id":"ENSG00000177462.7","gene_symbol":"OR2T8","gene_name":"olfactory receptor family 2 subfamily T member 8 [Source:HGNC Symbol;Acc:HGNC:15020]","synonyms":"OR2T8P","biotype":"protein_coding","ncbi_id":"343172","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247920252,"end":247921956,"strand":1,"description":"olfactory receptor family 2 subfamily T member 8 [Source:HGNC Symbol;Acc:HGNC:15020]"}, {"versioned_ensembl_gene_id":"ENSG00000250238.1","gene_symbol":"AC253576.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105959,"end":107114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271228.1","gene_symbol":"AL121655.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32013061,"end":32013368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184489.11","gene_symbol":"PTP4A3","gene_name":"protein tyrosine phosphatase type IVA, member 3 [Source:HGNC Symbol;Acc:HGNC:9636]","synonyms":"PRL3,PRL-R,PRL-3","biotype":"protein_coding","ncbi_id":"11156","summary":"This gene encodes a member of the protein-tyrosine phosphatase family. Protein tyrosine phosphatases are cell signaling molecules that play regulatory roles in a variety of cellular processes. Studies of this class of protein tyrosine phosphatase in mice demonstrates that they are prenylated in vivo, suggesting their association with cell plasma membrane. The encoded protein may enhance cell proliferation, and overexpression of this gene has been implicated in tumor metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":141391993,"end":141432454,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 3 [Source:HGNC Symbol;Acc:HGNC:9636]"}, {"versioned_ensembl_gene_id":"ENSG00000253416.1","gene_symbol":"AC023200.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76904591,"end":76913399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260209.1","gene_symbol":"AP000842.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125873031,"end":125874528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280660.1","gene_symbol":"AL157396.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93762453,"end":93771991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270623.1","gene_symbol":"SPCS2P2","gene_name":"signal peptidase complex subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45235]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644573","summary":null,"start":100143065,"end":100143995,"strand":-1,"description":"signal peptidase complex subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45235]"}, {"versioned_ensembl_gene_id":"ENSG00000213279.2","gene_symbol":"Z97192.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49572264,"end":49575426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235111.1","gene_symbol":"Z97192.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49612657,"end":49615716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223360.1","gene_symbol":"AC096559.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12598987,"end":12605145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280345.1","gene_symbol":"AC092184.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8631545,"end":8632259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232519.2","gene_symbol":"AL353807.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155609776,"end":155610380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233995.1","gene_symbol":"AP000547.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16572027,"end":16574637,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188403.7","gene_symbol":"IGHV1OR15-9","gene_name":"immunoglobulin heavy variable 1/OR15-9 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5569]","synonyms":"VSIG7,IGHV1OR159,IGHV1/OR15-9","biotype":"IG_V_gene","ncbi_id":"390531","summary":null,"start":19964666,"end":19965101,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-9 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5569]"}, {"versioned_ensembl_gene_id":"ENSG00000100092.20","gene_symbol":"SH3BP1","gene_name":"SH3 domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10824]","synonyms":"ARHGAP43","biotype":"protein_coding","ncbi_id":"23616","summary":"This gene encodes a member of the Rho GTPase activating protein (RhoGAP) family. The encoded protein regulates Rac signaling and plays a role in cytoskeletal dynamics, cell motility and epithelial junction formation. This protein's association with the exocyst complex, which tethers secretory vesicles to the plasma membrane, has been demonstrated to be important in cell motility. In a distinct complex, this protein has been shown to regulate epithelial junction formation and morphogenesis. By interacting with the Plexin-D1 cell surface receptor, this protein mediates changes in the cytoskeleton in response to semaphorin binding. This protein may promote metastasis in human liver cancer cells and tissues. [provided by RefSeq, Mar 2017]","start":37634654,"end":37666932,"strand":1,"description":"SH3 domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10824]"}, {"versioned_ensembl_gene_id":"ENSG00000130755.12","gene_symbol":"GMFG","gene_name":"glia maturation factor gamma [Source:HGNC Symbol;Acc:HGNC:4374]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9535","summary":null,"start":39328353,"end":39342372,"strand":-1,"description":"glia maturation factor gamma [Source:HGNC Symbol;Acc:HGNC:4374]"}, {"versioned_ensembl_gene_id":"ENSG00000227032.1","gene_symbol":"RPS2P36","gene_name":"ribosomal protein S2 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271243","summary":null,"start":96620877,"end":96621707,"strand":-1,"description":"ribosomal protein S2 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36784]"}, {"versioned_ensembl_gene_id":"ENSG00000235969.1","gene_symbol":"CHEK2P4","gene_name":"checkpoint kinase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43580]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479021","summary":null,"start":16503304,"end":16509475,"strand":1,"description":"checkpoint kinase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43580]"}, {"versioned_ensembl_gene_id":"ENSG00000138083.4","gene_symbol":"SIX3","gene_name":"SIX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:10889]","synonyms":"HPE2","biotype":"protein_coding","ncbi_id":"6496","summary":"This gene encodes a member of the sine oculis homeobox transcription factor family. The encoded protein plays a role in eye development. Mutations in this gene have been associated with holoprosencephaly type 2. [provided by RefSeq, Oct 2009]","start":44941898,"end":44946077,"strand":1,"description":"SIX homeobox 3 [Source:HGNC Symbol;Acc:HGNC:10889]"}, {"versioned_ensembl_gene_id":"ENSG00000119203.13","gene_symbol":"CPSF3","gene_name":"cleavage and polyadenylation specific factor 3 [Source:HGNC Symbol;Acc:HGNC:2326]","synonyms":"YSH1,CPSF73,CPSF-73","biotype":"protein_coding","ncbi_id":"51692","summary":"This gene encodes a member of the metallo-beta-lactamase family. The encoded protein is a 73kDa subunit of the cleavage and polyadenylation specificity factor and functions as an endonuclease that recognizes the pre-mRNA 3'-cleavage site AAUAAA prior to polyadenylation. It also cleaves after the pre-mRNA sequence ACCCA during histone 3'-end pre-mRNA processing. [provided by RefSeq, Oct 2012]","start":9423568,"end":9473101,"strand":1,"description":"cleavage and polyadenylation specific factor 3 [Source:HGNC Symbol;Acc:HGNC:2326]"}, {"versioned_ensembl_gene_id":"ENSG00000225675.2","gene_symbol":"LINC01771","gene_name":"long intergenic non-protein coding RNA 1771 [Source:HGNC Symbol;Acc:HGNC:52561]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378732","summary":null,"start":53328233,"end":53336509,"strand":1,"description":"long intergenic non-protein coding RNA 1771 [Source:HGNC Symbol;Acc:HGNC:52561]"}, {"versioned_ensembl_gene_id":"ENSG00000275051.2","gene_symbol":"PIWIL1","gene_name":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]","synonyms":"PIWI,HIWI,CT80.1","biotype":"protein_coding","ncbi_id":"9271","summary":"This gene encodes a member of the PIWI subfamily of Argonaute proteins, evolutionarily conserved proteins containing both PAZ and Piwi motifs that play important roles in stem cell self-renewal, RNA silencing, and translational regulation in diverse organisms. The encoded protein may play a role as an intrinsic regulator of the self-renewal capacity of germline and hematopoietic stem cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":130337887,"end":130372618,"strand":1,"description":"piwi like RNA-mediated gene silencing 1 [Source:HGNC Symbol;Acc:HGNC:9007]"}, {"versioned_ensembl_gene_id":"ENSG00000120685.19","gene_symbol":"PROSER1","gene_name":"proline and serine rich 1 [Source:HGNC Symbol;Acc:HGNC:20291]","synonyms":"FLJ12661,C13orf23,bA50D16.2","biotype":"protein_coding","ncbi_id":"80209","summary":"This gene encodes a conserved protein containing proline and serine rich regions. These regions may be important in protein-protein interactions. [provided by RefSeq, Aug 2012]","start":39009866,"end":39038076,"strand":-1,"description":"proline and serine rich 1 [Source:HGNC Symbol;Acc:HGNC:20291]"}, {"versioned_ensembl_gene_id":"ENSG00000228466.1","gene_symbol":"TUBB4AP1","gene_name":"tubulin beta 4A class IVa pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402422","summary":null,"start":123561642,"end":123562966,"strand":1,"description":"tubulin beta 4A class IVa pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42340]"}, {"versioned_ensembl_gene_id":"ENSG00000227873.1","gene_symbol":"Z93242.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17769005,"end":17769398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234371.6","gene_symbol":"RPSAP31","gene_name":"ribosomal protein SA pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35558]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"391598","summary":null,"start":183884924,"end":183888449,"strand":1,"description":"ribosomal protein SA pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35558]"}, {"versioned_ensembl_gene_id":"ENSG00000284430.1","gene_symbol":"AC020912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31100304,"end":31147981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231724.1","gene_symbol":"AC112907.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186807692,"end":186818121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265844.1","gene_symbol":"AC100863.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77180106,"end":77235430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235550.1","gene_symbol":"ANKRD26P2","gene_name":"ankyrin repeat domain 26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39687]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646929","summary":null,"start":38922727,"end":38936199,"strand":-1,"description":"ankyrin repeat domain 26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39687]"}, {"versioned_ensembl_gene_id":"ENSG00000279225.1","gene_symbol":"AC138305.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":63397707,"end":63397946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146587.17","gene_symbol":"RBAK","gene_name":"RB associated KRAB zinc finger [Source:HGNC Symbol;Acc:HGNC:17680]","synonyms":"ZNF769","biotype":"protein_coding","ncbi_id":"57786","summary":"This gene encodes a nuclear protein which interacts with the tumor suppressor retinoblastoma 1. The two interacting proteins are thought to act as a transcriptional repressor for promoters which are activated by the E2F1 transcription factor. This protein contains a Kruppel-associated box (KRAB), which is a transcriptional repressor motif. Read-through transcripts that include exons from the downstream gene LOC389458 are expressed from this locus. [provided by RefSeq, Mar 2011]","start":5045821,"end":5069488,"strand":1,"description":"RB associated KRAB zinc finger [Source:HGNC Symbol;Acc:HGNC:17680]"}, {"versioned_ensembl_gene_id":"ENSG00000272864.1","gene_symbol":"AC135803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74698769,"end":74699333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213977.7","gene_symbol":"TAX1BP3","gene_name":"Tax1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:30684]","synonyms":"TIP-1","biotype":"protein_coding","ncbi_id":"30851","summary":"This gene encodes a small, highly conserved protein with a single PDZ domain. PDZ (PSD-95/Discs large/ZO-1 homologous) domains promote protein-protein interactions that affect cell signaling, adhesion, protein scaffolding, and receptor and ion transporter functions. The encoded protein interacts with a large number of target proteins that play roles in signaling pathways; for example, it interacts with Rho A and glutaminase L and also acts as a negative regulator of the Wnt/beta-catenin signaling pathway. This protein was first identified as binding to the T-cell leukaemia virus (HTLV1) Tax oncoprotein. Overexpression of this gene has been implicated in altered cancer cell adhesion, migration and metastasis. The encoded protein also modulates the localization and density of inwardly rectifying potassium channel 2.3 (Kir2.3). To date, this protein has been shown to play a role in cell proliferation, development, stress response, and polarization. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]","start":3662896,"end":3668682,"strand":-1,"description":"Tax1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:30684]"}, {"versioned_ensembl_gene_id":"ENSG00000155363.18","gene_symbol":"MOV10","gene_name":"Mov10 RISC complex RNA helicase [Source:HGNC Symbol;Acc:HGNC:7200]","synonyms":"MGC2948,gb110,fSAP113","biotype":"protein_coding","ncbi_id":"4343","summary":null,"start":112673141,"end":112700746,"strand":1,"description":"Mov10 RISC complex RNA helicase [Source:HGNC Symbol;Acc:HGNC:7200]"}, {"versioned_ensembl_gene_id":"ENSG00000174016.11","gene_symbol":"FAM46D","gene_name":"family with sequence similarity 46 member D [Source:HGNC Symbol;Acc:HGNC:28399]","synonyms":"MGC26999,CT112,CT1.26","biotype":"protein_coding","ncbi_id":"169966","summary":"Antibodies against the protein encoded by this gene were found only in plasma from cancer patients. While it may be a target for immunotherapy, the function of this gene is unknown. [provided by RefSeq, Dec 2009]","start":80335504,"end":80445311,"strand":1,"description":"family with sequence similarity 46 member D [Source:HGNC Symbol;Acc:HGNC:28399]"}, {"versioned_ensembl_gene_id":"ENSG00000270654.1","gene_symbol":"NUTF2P8","gene_name":"nuclear transport factor 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50457]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287183","summary":null,"start":21362292,"end":21364025,"strand":-1,"description":"nuclear transport factor 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:50457]"}, {"versioned_ensembl_gene_id":"ENSG00000112308.12","gene_symbol":"C6orf62","gene_name":"chromosome 6 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:20998]","synonyms":"XTP12,FLJ12619,DKFZP564G182","biotype":"protein_coding","ncbi_id":"81688","summary":null,"start":24704861,"end":24720836,"strand":-1,"description":"chromosome 6 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:20998]"}, {"versioned_ensembl_gene_id":"ENSG00000151632.17","gene_symbol":"AKR1C2","gene_name":"aldo-keto reductase family 1 member C2 [Source:HGNC Symbol;Acc:HGNC:385]","synonyms":"TDD,MCDR2,HAKRD,DDH2,DD2,DD,BABP","biotype":"protein_coding","ncbi_id":"1646","summary":"This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols using NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme binds bile acid with high affinity, and shows minimal 3-alpha-hydroxysteroid dehydrogenase activity. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":4987400,"end":5018031,"strand":-1,"description":"aldo-keto reductase family 1 member C2 [Source:HGNC Symbol;Acc:HGNC:385]"}, {"versioned_ensembl_gene_id":"ENSG00000225025.2","gene_symbol":"KIF4CP","gene_name":"kinesin family member 4C, pseudogene [Source:HGNC Symbol;Acc:HGNC:13340]","synonyms":"KIF4P1","biotype":"processed_pseudogene","ncbi_id":"347363","summary":null,"start":79323446,"end":79325217,"strand":1,"description":"kinesin family member 4C, pseudogene [Source:HGNC Symbol;Acc:HGNC:13340]"}, {"versioned_ensembl_gene_id":"ENSG00000270231.3","gene_symbol":"NBPF8","gene_name":"NBPF member 8 [Source:HGNC Symbol;Acc:HGNC:31990]","synonyms":"NBPF8P","biotype":"unprocessed_pseudogene","ncbi_id":"728841","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2013]","start":120436353,"end":120467739,"strand":1,"description":"NBPF member 8 [Source:HGNC Symbol;Acc:HGNC:31990]"}, {"versioned_ensembl_gene_id":"ENSG00000178965.13","gene_symbol":"ERICH3","gene_name":"glutamate rich 3 [Source:HGNC Symbol;Acc:HGNC:25346]","synonyms":"RP11-653A5.1,DKFZp547I048,C1orf173","biotype":"protein_coding","ncbi_id":"127254","summary":null,"start":74568111,"end":74673738,"strand":-1,"description":"glutamate rich 3 [Source:HGNC Symbol;Acc:HGNC:25346]"}, {"versioned_ensembl_gene_id":"ENSG00000275338.4","gene_symbol":"RAB11FIP3","gene_name":"RAB11 family interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:17224]","synonyms":"Rab11-FIP3,KIAA0665,eferin","biotype":"protein_coding","ncbi_id":"9727","summary":"Proteins of the large Rab GTPase family (see RAB1A; MIM 179508) have regulatory roles in the formation, targeting, and fusion of intracellular transport vesicles. RAB11FIP3 is one of many proteins that interact with and regulate Rab GTPases (Hales et al., 2001 [PubMed 11495908]).[supplied by OMIM, Mar 2008]","start":425619,"end":526533,"strand":1,"description":"RAB11 family interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:17224]"}, {"versioned_ensembl_gene_id":"ENSG00000079102.16","gene_symbol":"RUNX1T1","gene_name":"RUNX1 translocation partner 1 [Source:HGNC Symbol;Acc:HGNC:1535]","synonyms":"ZMYND2,MTG8,ETO,CDR,CBFA2T1,AML1T1","biotype":"protein_coding","ncbi_id":"862","summary":"This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]","start":91954967,"end":92103286,"strand":-1,"description":"RUNX1 translocation partner 1 [Source:HGNC Symbol;Acc:HGNC:1535]"}, {"versioned_ensembl_gene_id":"ENSG00000278594.1","gene_symbol":"AL589182.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19131842,"end":19132890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157927.16","gene_symbol":"RADIL","gene_name":"Rap associating with DIL domain [Source:HGNC Symbol;Acc:HGNC:22226]","synonyms":"RASIP2,KIAA1849,FLJ10324","biotype":"protein_coding","ncbi_id":"55698","summary":null,"start":4797055,"end":4883719,"strand":-1,"description":"Rap associating with DIL domain [Source:HGNC Symbol;Acc:HGNC:22226]"}, {"versioned_ensembl_gene_id":"ENSG00000236999.1","gene_symbol":"ATP2B2-IT1","gene_name":"ATP2B2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41309]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874324","summary":null,"start":10566255,"end":10570375,"strand":-1,"description":"ATP2B2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41309]"}, {"versioned_ensembl_gene_id":"ENSG00000248986.1","gene_symbol":"AC104825.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8320279,"end":8323965,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066813.14","gene_symbol":"ACSM2B","gene_name":"acyl-CoA synthetase medium chain family member 2B [Source:HGNC Symbol;Acc:HGNC:30931]","synonyms":"ACSM2,HYST1046,HXMA","biotype":"protein_coding","ncbi_id":"348158","summary":null,"start":20536226,"end":20576427,"strand":-1,"description":"acyl-CoA synthetase medium chain family member 2B [Source:HGNC Symbol;Acc:HGNC:30931]"}, {"versioned_ensembl_gene_id":"ENSG00000227773.1","gene_symbol":"ASH1L-IT1","gene_name":"ASH1L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41449]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478976","summary":null,"start":155396010,"end":155396978,"strand":-1,"description":"ASH1L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41449]"}, {"versioned_ensembl_gene_id":"ENSG00000236666.1","gene_symbol":"POTEH-AS1","gene_name":"POTEH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40058]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100852406","summary":null,"start":15699361,"end":15703403,"strand":-1,"description":"POTEH antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40058]"}, {"versioned_ensembl_gene_id":"ENSG00000228988.1","gene_symbol":"AL353771.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70218589,"end":70221023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264486.1","gene_symbol":"AC061975.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28256438,"end":28265551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260777.1","gene_symbol":"AC061975.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28263634,"end":28266369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262237.1","gene_symbol":"AL157402.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":198669040,"end":198678548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278403.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54922093,"end":54938887,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000184319.15","gene_symbol":"RPL23AP82","gene_name":"ribosomal protein L23a pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:33730]","synonyms":"MGC70863","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284942","summary":null,"start":50756948,"end":50801309,"strand":1,"description":"ribosomal protein L23a pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:33730]"}, {"versioned_ensembl_gene_id":"ENSG00000234145.1","gene_symbol":"NAP1L4P3","gene_name":"nucleosome assembly protein 1 like 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39738]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730174","summary":null,"start":47763460,"end":47764606,"strand":1,"description":"nucleosome assembly protein 1 like 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39738]"}, {"versioned_ensembl_gene_id":"ENSG00000280306.1","gene_symbol":"AC137056.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":20487702,"end":20489659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253105.5","gene_symbol":"AP003548.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96371865,"end":96387438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238211.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"AB023060.6,POLR2LP","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31140727,"end":31140913,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000237005.1","gene_symbol":"HIGD1AP15","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:43010]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289605","summary":null,"start":10334419,"end":10334698,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:43010]"}, {"versioned_ensembl_gene_id":"ENSG00000139620.12","gene_symbol":"KANSL2","gene_name":"KAT8 regulatory NSL complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:26024]","synonyms":"NSL2,FLJ20436,C12orf41","biotype":"protein_coding","ncbi_id":"54934","summary":null,"start":48653401,"end":48682238,"strand":-1,"description":"KAT8 regulatory NSL complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:26024]"}, {"versioned_ensembl_gene_id":"ENSG00000116604.17","gene_symbol":"MEF2D","gene_name":"myocyte enhancer factor 2D [Source:HGNC Symbol;Acc:HGNC:6997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4209","summary":"This gene is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Members of this family are involved in control of muscle and neuronal cell differentiation and development, and are regulated by class II histone deacetylases. Fusions of the encoded protein with Deleted in Azoospermia-Associated Protein 1 (DAZAP1) due to a translocation have been found in an acute lymphoblastic leukemia cell line, suggesting a role in leukemogenesis. The encoded protein may also be involved in Parkinson disease and myotonic dystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":156463727,"end":156500828,"strand":-1,"description":"myocyte enhancer factor 2D [Source:HGNC Symbol;Acc:HGNC:6997]"}, {"versioned_ensembl_gene_id":"ENSG00000251544.1","gene_symbol":"MTND5P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873257","summary":null,"start":94567461,"end":94568909,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42274]"}, {"versioned_ensembl_gene_id":"ENSG00000270133.1","gene_symbol":"AC025766.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":94611906,"end":94618122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132639.12","gene_symbol":"SNAP25","gene_name":"synaptosome associated protein 25 [Source:HGNC Symbol;Acc:HGNC:11132]","synonyms":"SNAP-25,SNAP,SEC9,RIC4,RIC-4,dJ1068F16.2,bA416N4.2","biotype":"protein_coding","ncbi_id":"6616","summary":"Synaptic vesicle membrane docking and fusion is mediated by SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) located on the vesicle membrane (v-SNAREs) and the target membrane (t-SNAREs). The assembled v-SNARE/t-SNARE complex consists of a bundle of four helices, one of which is supplied by v-SNARE and the other three by t-SNARE. For t-SNAREs on the plasma membrane, the protein syntaxin supplies one helix and the protein encoded by this gene contributes the other two. Therefore, this gene product is a presynaptic plasma membrane protein involved in the regulation of neurotransmitter release. Two alternative transcript variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":10218830,"end":10307418,"strand":1,"description":"synaptosome associated protein 25 [Source:HGNC Symbol;Acc:HGNC:11132]"}, {"versioned_ensembl_gene_id":"ENSG00000236886.2","gene_symbol":"AC007563.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":216694464,"end":216994079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121318.2","gene_symbol":"TAS2R10","gene_name":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]","synonyms":"T2R10,TRB2","biotype":"protein_coding","ncbi_id":"50839","summary":"This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]","start":10825317,"end":10826358,"strand":-1,"description":"taste 2 receptor member 10 [Source:HGNC Symbol;Acc:HGNC:14918]"}, {"versioned_ensembl_gene_id":"ENSG00000212125.2","gene_symbol":"TAS2R15P","gene_name":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]","synonyms":"PS8,TAS2R15,T2R15","biotype":"processed_pseudogene","ncbi_id":"266657","summary":null,"start":10964425,"end":10965352,"strand":-1,"description":"taste 2 receptor member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:19106]"}, {"versioned_ensembl_gene_id":"ENSG00000236295.1","gene_symbol":"AC007557.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216870441,"end":216873932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284687.1","gene_symbol":"AC092865.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8390270,"end":8390488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263029.1","gene_symbol":"AC136624.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16260866,"end":16261235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225921.6","gene_symbol":"NOL7","gene_name":"nucleolar protein 7 [Source:HGNC Symbol;Acc:HGNC:21040]","synonyms":"RARG-1,PQBP3,NOP27,dJ223E5.2,C6orf90","biotype":"protein_coding","ncbi_id":"51406","summary":"The protein encoded by this gene localizes to the nucleolus, where it maintains nucleolar structure and cell growth rates. The encoded protein also functions as a tumor suppressor and regulator of angiogenesis. The RB tumor suppressor gene recruits transcription factors to this gene and positively regulates its expression. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015]","start":13615327,"end":13632739,"strand":1,"description":"nucleolar protein 7 [Source:HGNC Symbol;Acc:HGNC:21040]"}, {"versioned_ensembl_gene_id":"ENSG00000279024.1","gene_symbol":"AC112255.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":136230753,"end":136233245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172175.12","gene_symbol":"MALT1","gene_name":"MALT1 paracaspase [Source:HGNC Symbol;Acc:HGNC:6819]","synonyms":"PCASP1,MLT","biotype":"protein_coding","ncbi_id":"10892","summary":"This gene encodes a caspase-like protease that plays a role in BCL10-induced activation of NF-kappaB. The protein is a component of the CARMA1-BCL10-MALT1 (CBM) signalosome that triggers NF-kappaB signaling and lymphoctye activation following antigen-receptor stimulation. Mutations in this gene result in immunodeficiency 12 (IMD12). This gene has been found to be recurrently rearranged in chromosomal translocations with other genes in mucosa-associated lymphoid tissue lymphomas, including a t(11;18)(q21;q21) translocation with the baculoviral IAP repeat-containing protein 3 (also known as apoptosis inhibitor 2) locus [BIRC3(API2)-MALT1], and a t(14;18)(q32;q21) translocation with the immunoglobulin heavy chain locus (IGH-MALT1). Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2018]","start":58671386,"end":58754477,"strand":1,"description":"MALT1 paracaspase [Source:HGNC Symbol;Acc:HGNC:6819]"}, {"versioned_ensembl_gene_id":"ENSG00000229505.1","gene_symbol":"AC104455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86029854,"end":86030589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267476.1","gene_symbol":"AC104365.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58672613,"end":58752730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168259.14","gene_symbol":"DNAJC7","gene_name":"DnaJ heat shock protein family (Hsp40) member C7 [Source:HGNC Symbol;Acc:HGNC:12392]","synonyms":"TTC2,TPR2","biotype":"protein_coding","ncbi_id":"7266","summary":"This gene encodes a member of the DNAJ heat shock protein 40 family of proteins that is characterized by two N-terminal tetratricopeptide repeat domains and a C-terminal DNAJ domain. This protein binds the chaperone proteins heat shock proteins 70 and 90 in an ATP-dependent manner and may function as a co-chaperone. Pseudogenes of this gene are found on chromosomes 1 and 6. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":41976433,"end":42021376,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C7 [Source:HGNC Symbol;Acc:HGNC:12392]"}, {"versioned_ensembl_gene_id":"ENSG00000234287.1","gene_symbol":"AC099560.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40761545,"end":40761799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281360.1","gene_symbol":"AC231647.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197458404,"end":197468515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227814.3","gene_symbol":"MRPS17P9","gene_name":"mitochondrial ribosomal protein S17 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:29739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359760","summary":null,"start":119379712,"end":119380104,"strand":1,"description":"mitochondrial ribosomal protein S17 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:29739]"}, {"versioned_ensembl_gene_id":"ENSG00000135617.3","gene_symbol":"PRADC1","gene_name":"protease associated domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16047]","synonyms":"PAP21,MGC13004,hPAP21,C2orf7","biotype":"protein_coding","ncbi_id":"84279","summary":null,"start":73228006,"end":73233238,"strand":-1,"description":"protease associated domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16047]"}, {"versioned_ensembl_gene_id":"ENSG00000232750.2","gene_symbol":"AL139132.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179035309,"end":179035652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227804.7","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"PNUTS,CAT53,p99,FB19","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30590637,"end":30608849,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000163534.14","gene_symbol":"FCRL1","gene_name":"Fc receptor like 1 [Source:HGNC Symbol;Acc:HGNC:18509]","synonyms":"CD307a,IRTA5,IFGP1,FCRH1","biotype":"protein_coding","ncbi_id":"115350","summary":"This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains three extracellular C2-like immunoglobulin domains, a transmembrane domain and a cytoplasmic domain with two immunoreceptor-tyrosine activation motifs. This protein may play a role in the regulation of cancer cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":157794403,"end":157820105,"strand":-1,"description":"Fc receptor like 1 [Source:HGNC Symbol;Acc:HGNC:18509]"}, {"versioned_ensembl_gene_id":"ENSG00000237879.1","gene_symbol":"LINC00398","gene_name":"long intergenic non-protein coding RNA 398 [Source:HGNC Symbol;Acc:HGNC:42727]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874158","summary":null,"start":30803206,"end":30810645,"strand":1,"description":"long intergenic non-protein coding RNA 398 [Source:HGNC Symbol;Acc:HGNC:42727]"}, {"versioned_ensembl_gene_id":"ENSG00000277514.1","gene_symbol":"AC025016.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":5903767,"end":5904448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279976.1","gene_symbol":"AC073862.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130962175,"end":130963028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173786.16","gene_symbol":"CNP","gene_name":"2',3'-cyclic nucleotide 3' phosphodiesterase [Source:HGNC Symbol;Acc:HGNC:2158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1267","summary":null,"start":41966741,"end":41977731,"strand":1,"description":"2',3'-cyclic nucleotide 3' phosphodiesterase [Source:HGNC Symbol;Acc:HGNC:2158]"}, {"versioned_ensembl_gene_id":"ENSG00000232293.2","gene_symbol":"PAICSP7","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780816","summary":null,"start":94636663,"end":94639570,"strand":-1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38100]"}, {"versioned_ensembl_gene_id":"ENSG00000274717.1","gene_symbol":"AL049757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42791814,"end":42794313,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228536.2","gene_symbol":"AL513283.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219409523,"end":219459369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228277.1","gene_symbol":"AC112518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73710302,"end":73714527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204479.4","gene_symbol":"PRAMEF17","gene_name":"PRAME family member 17 [Source:HGNC Symbol;Acc:HGNC:29485]","synonyms":"OTTHUMG00000007909","biotype":"protein_coding","ncbi_id":"391004","summary":null,"start":13389632,"end":13392629,"strand":1,"description":"PRAME family member 17 [Source:HGNC Symbol;Acc:HGNC:29485]"}, {"versioned_ensembl_gene_id":"ENSG00000204960.6","gene_symbol":"BLACE","gene_name":"B-cell acute lymphoblastic leukemia expressed [Source:HGNC Symbol;Acc:HGNC:20484]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338436","summary":null,"start":155356985,"end":155367934,"strand":-1,"description":"B-cell acute lymphoblastic leukemia expressed [Source:HGNC Symbol;Acc:HGNC:20484]"}, {"versioned_ensembl_gene_id":"ENSG00000260471.1","gene_symbol":"AC009120.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74220929,"end":74221427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196576.14","gene_symbol":"PLXNB2","gene_name":"plexin B2 [Source:HGNC Symbol;Acc:HGNC:9104]","synonyms":"PLEXB2,MM1,KIAA0315","biotype":"protein_coding","ncbi_id":"23654","summary":"Members of the B class of plexins, such as PLXNB2 are transmembrane receptors that participate in axon guidance and cell migration in response to semaphorins (Perrot et al. (2002) [PubMed 12183458]).[supplied by OMIM, Mar 2008]","start":50274979,"end":50307627,"strand":-1,"description":"plexin B2 [Source:HGNC Symbol;Acc:HGNC:9104]"}, {"versioned_ensembl_gene_id":"ENSG00000135503.12","gene_symbol":"ACVR1B","gene_name":"activin A receptor type 1B [Source:HGNC Symbol;Acc:HGNC:172]","synonyms":"ALK4,ACVRLK4,ActRIB,SKR2","biotype":"protein_coding","ncbi_id":"91","summary":"This gene encodes an activin A type IB receptor. Activins are dimeric growth and differentiation factors which belong to the transforming growth factor-beta (TGF-beta) superfamily of structurally related signaling proteins. Activins signal through a heteromeric complex of receptor serine kinases which include at least two type I and two type II receptors. This protein is a type I receptor which is essential for signaling. Mutations in this gene are associated with pituitary tumors. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]","start":51951667,"end":51997078,"strand":1,"description":"activin A receptor type 1B [Source:HGNC Symbol;Acc:HGNC:172]"}, {"versioned_ensembl_gene_id":"ENSG00000226998.1","gene_symbol":"MTATP6P30","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52185]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075302","summary":null,"start":31505280,"end":31505943,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52185]"}, {"versioned_ensembl_gene_id":"ENSG00000260720.1","gene_symbol":"LINC01243","gene_name":"long intergenic non-protein coding RNA 1243 [Source:HGNC Symbol;Acc:HGNC:49814]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929620","summary":null,"start":31371611,"end":31381490,"strand":-1,"description":"long intergenic non-protein coding RNA 1243 [Source:HGNC Symbol;Acc:HGNC:49814]"}, {"versioned_ensembl_gene_id":"ENSG00000128274.15","gene_symbol":"A4GALT","gene_name":"alpha 1,4-galactosyltransferase (P blood group) [Source:HGNC Symbol;Acc:HGNC:18149]","synonyms":"P(k),Gb3S,A14GALT,P1","biotype":"protein_coding","ncbi_id":"53947","summary":"The protein encoded by this gene catalyzes the transfer of galactose to lactosylceramide to form globotriaosylceramide, which has been identified as the P(k) antigen of the P blood group system. This protein, a type II membrane protein found in the Golgi, is also required for the synthesis of the bacterial verotoxins receptor. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":42692121,"end":42721298,"strand":-1,"description":"alpha 1,4-galactosyltransferase (P blood group) [Source:HGNC Symbol;Acc:HGNC:18149]"}, {"versioned_ensembl_gene_id":"ENSG00000259817.2","gene_symbol":"AC087565.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73812621,"end":73816053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279120.1","gene_symbol":"AC009033.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73293866,"end":73294296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261227.2","gene_symbol":"AC140912.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73232055,"end":73233970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158623.14","gene_symbol":"COPG2","gene_name":"coatomer protein complex subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:2237]","synonyms":"2-COP","biotype":"protein_coding","ncbi_id":"26958","summary":null,"start":130506238,"end":130668748,"strand":-1,"description":"coatomer protein complex subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:2237]"}, {"versioned_ensembl_gene_id":"ENSG00000235828.5","gene_symbol":"AC005550.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15701435,"end":15701752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197879.14","gene_symbol":"MYO1C","gene_name":"myosin IC [Source:HGNC Symbol;Acc:HGNC:7597]","synonyms":"myr2","biotype":"protein_coding","ncbi_id":"4641","summary":"This gene encodes a member of the unconventional myosin protein family, which are actin-based molecular motors. The protein is found in the cytoplasm, and one isoform with a unique N-terminus is also found in the nucleus. The nuclear isoform associates with RNA polymerase I and II and functions in transcription initiation. The mouse ortholog of this protein also functions in intracellular vesicle transport to the plasma membrane. Multiple transcript variants encoding different isoforms have been found for this gene. The related gene myosin IE has been referred to as myosin IC in the literature, but it is a distinct locus on chromosome 19. [provided by RefSeq, Jul 2008]","start":1464098,"end":1492812,"strand":-1,"description":"myosin IC [Source:HGNC Symbol;Acc:HGNC:7597]"}, {"versioned_ensembl_gene_id":"ENSG00000254093.8","gene_symbol":"PINX1","gene_name":"PIN2/TERF1 interacting telomerase inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:30046]","synonyms":"Pxr1,PinX1,MGC8850,LPTS,LPTL,Gno1,FLJ20565","biotype":"protein_coding","ncbi_id":"54984","summary":null,"start":10764963,"end":10839884,"strand":-1,"description":"PIN2/TERF1 interacting telomerase inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:30046]"}, {"versioned_ensembl_gene_id":"ENSG00000227695.5","gene_symbol":"DNMBP-AS1","gene_name":"DNMBP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20431]","synonyms":"NCRNA00093,FLJ40792,bA287G8.2","biotype":"antisense_RNA","ncbi_id":"100188954","summary":null,"start":99927010,"end":99958381,"strand":1,"description":"DNMBP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20431]"}, {"versioned_ensembl_gene_id":"ENSG00000220785.7","gene_symbol":"MTMR9LP","gene_name":"myotubularin related protein 9-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:27920]","synonyms":"MTMR9L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339483","summary":null,"start":32231658,"end":32241620,"strand":-1,"description":"myotubularin related protein 9-like, pseudogene [Source:HGNC Symbol;Acc:HGNC:27920]"}, {"versioned_ensembl_gene_id":"ENSG00000270100.1","gene_symbol":"AC012065.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20678254,"end":20678932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240677.1","gene_symbol":"MYL6P4","gene_name":"myosin light chain 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37813]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642627","summary":null,"start":141811805,"end":141812257,"strand":1,"description":"myosin light chain 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37813]"}, {"versioned_ensembl_gene_id":"ENSG00000198106.8","gene_symbol":"AC025279.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29291220,"end":29372110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279106.1","gene_symbol":"AC009093.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29204633,"end":29205855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182824.7","gene_symbol":"LINC01662","gene_name":"long intergenic non-protein coding RNA 1662 [Source:HGNC Symbol;Acc:HGNC:52450]","synonyms":null,"biotype":"lincRNA","ncbi_id":"642643","summary":null,"start":18733914,"end":18757906,"strand":1,"description":"long intergenic non-protein coding RNA 1662 [Source:HGNC Symbol;Acc:HGNC:52450]"}, {"versioned_ensembl_gene_id":"ENSG00000179119.14","gene_symbol":"SPTY2D1","gene_name":"SPT2 chromatin protein domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26818]","synonyms":"Spt2,FLJ39441,DKFZp686I068","biotype":"protein_coding","ncbi_id":"144108","summary":null,"start":18606401,"end":18634791,"strand":-1,"description":"SPT2 chromatin protein domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26818]"}, {"versioned_ensembl_gene_id":"ENSG00000230682.1","gene_symbol":"GRPEL2P3","gene_name":"GrpE like 2, mitochondrial pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41971]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129871","summary":null,"start":94782886,"end":94783525,"strand":1,"description":"GrpE like 2, mitochondrial pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41971]"}, {"versioned_ensembl_gene_id":"ENSG00000223438.1","gene_symbol":"AC235097.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":141625864,"end":141626733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198573.6","gene_symbol":"SPANXC","gene_name":"SPANX family member C [Source:HGNC Symbol;Acc:HGNC:14331]","synonyms":"CTp11,CT11.3","biotype":"protein_coding","ncbi_id":"64663","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family, which is located in a gene cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene encodes a protein that localizes to the nucleus and is expressed in highly metastatic cell lines, making the protein a potential diagnostic and prognostic marker. The protein belongs to a family of cancer/testis antigens and represents a potential target for cancer immunotherapy. [provided by RefSeq, Jul 2008]","start":141241463,"end":141242496,"strand":-1,"description":"SPANX family member C [Source:HGNC Symbol;Acc:HGNC:14331]"}, {"versioned_ensembl_gene_id":"ENSG00000126970.15","gene_symbol":"ZC4H2","gene_name":"zinc finger C4H2-type containing [Source:HGNC Symbol;Acc:HGNC:24931]","synonyms":"HCA127,WWS,KIAA1166","biotype":"protein_coding","ncbi_id":"55906","summary":"This gene encodes a member of the zinc finger domain-containing protein family. This family member has a C-terminal zinc finger domain that is characterized by four cysteine residues and two histidine residues, and it also includes a coiled-coil region. This protein has been detected as an autoantigen in hepatocellular carcinoma patients. This gene has been identified as a potential candidate for X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":64915802,"end":65034713,"strand":-1,"description":"zinc finger C4H2-type containing [Source:HGNC Symbol;Acc:HGNC:24931]"}, {"versioned_ensembl_gene_id":"ENSG00000280225.1","gene_symbol":"AC237221.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57402181,"end":57404717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253592.1","gene_symbol":"IGKV2-38","gene_name":"immunoglobulin kappa variable 2-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5787]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28917","summary":null,"start":89309898,"end":89310144,"strand":-1,"description":"immunoglobulin kappa variable 2-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5787]"}, {"versioned_ensembl_gene_id":"ENSG00000120903.12","gene_symbol":"CHRNA2","gene_name":"cholinergic receptor nicotinic alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:1956]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1135","summary":"Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels formed by a pentameric arrangement of alpha and beta subunits to create distinct muscle and neuronal receptors. Neuronal receptors are found throughout the peripheral and central nervous system where they are involved in fast synaptic transmission. This gene encodes an alpha subunit that is widely expressed in the brain. The proposed structure for nAChR subunits is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4. Single nucleotide polymorphisms (SNPs) in this gene have been associated with nicotine dependence. [provided by RefSeq, Nov 2009]","start":27459761,"end":27479883,"strand":-1,"description":"cholinergic receptor nicotinic alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:1956]"}, {"versioned_ensembl_gene_id":"ENSG00000129816.5","gene_symbol":"TTTY1B","gene_name":"testis-specific transcript, Y-linked 1B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37981]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100101116","summary":null,"start":6390431,"end":6411564,"strand":1,"description":"testis-specific transcript, Y-linked 1B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37981]"}, {"versioned_ensembl_gene_id":"ENSG00000143942.4","gene_symbol":"CHAC2","gene_name":"ChaC cation transport regulator homolog 2 [Source:HGNC Symbol;Acc:HGNC:32363]","synonyms":"GCG1","biotype":"protein_coding","ncbi_id":"494143","summary":"The protein encoded by this gene is a gamma-glutamyl cyclotransferase that catalyzes the conversion of glutathione to 5-oxoproline and cysteinylglycine. It is thought that this gene is upregulated in response to endoplasmic reticulum stress and that the glutathione depletion enhances apoptosis. [provided by RefSeq, Sep 2016]","start":53767792,"end":53775196,"strand":1,"description":"ChaC cation transport regulator homolog 2 [Source:HGNC Symbol;Acc:HGNC:32363]"}, {"versioned_ensembl_gene_id":"ENSG00000154710.16","gene_symbol":"RABGEF1","gene_name":"RAB guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:17676]","synonyms":"RABEX5,rabex-5,RABEX5,rabex-5","biotype":"protein_coding","ncbi_id":"27342","summary":"RABGEF1 forms a complex with rabaptin-5 (RABPT5; MIM 603616) that is required for endocytic membrane fusion, and it serves as a specific guanine nucleotide exchange factor (GEF) for RAB5 (RAB5A; MIM 179512) (Horiuchi et al., 1997 [PubMed 9323142]).[supplied by OMIM, Mar 2010]","start":66682164,"end":66811464,"strand":1,"description":"RAB guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:HGNC:17676]"}, {"versioned_ensembl_gene_id":"ENSG00000249540.1","gene_symbol":"AC117383.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141307612,"end":141307933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225912.1","gene_symbol":"AL121871.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92676519,"end":92676954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281964.1","gene_symbol":"IGHVIII-11-1","gene_name":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]","synonyms":"IGHV(III)-11-1","biotype":"IG_V_pseudogene","ncbi_id":"28352","summary":null,"start":106120978,"end":106121244,"strand":-1,"description":"immunoglobulin heavy variable (III)-11-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5692]"}, {"versioned_ensembl_gene_id":"ENSG00000246331.2","gene_symbol":"AC010198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30755074,"end":30780739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237179.5","gene_symbol":"LINC01797","gene_name":"long intergenic non-protein coding RNA 1797 [Source:HGNC Symbol;Acc:HGNC:52587]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927577","summary":null,"start":66697125,"end":66703227,"strand":-1,"description":"long intergenic non-protein coding RNA 1797 [Source:HGNC Symbol;Acc:HGNC:52587]"}, {"versioned_ensembl_gene_id":"ENSG00000271601.3","gene_symbol":"LIX1L","gene_name":"limb and CNS expressed 1 like [Source:HGNC Symbol;Acc:HGNC:28715]","synonyms":"MGC46719","biotype":"protein_coding","ncbi_id":"128077","summary":null,"start":145933423,"end":145958001,"strand":-1,"description":"limb and CNS expressed 1 like [Source:HGNC Symbol;Acc:HGNC:28715]"}, {"versioned_ensembl_gene_id":"ENSG00000282539.1","gene_symbol":"AC244131.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11208476,"end":11247646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204637.4","gene_symbol":"AC068538.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100509277,"end":100509612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127364.3","gene_symbol":"TAS2R4","gene_name":"taste 2 receptor member 4 [Source:HGNC Symbol;Acc:HGNC:14911]","synonyms":"T2R4","biotype":"protein_coding","ncbi_id":"50832","summary":"This gene encodes a member of a family of candidate taste receptors that are members of the G protein-coupled receptor superfamily and that are specifically expressed by taste receptor cells of the tongue and palate epithelia. These apparently intronless genes encode a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered with another 3 candidate taste receptor genes in chromosome 7 and is genetically linked to loci that influence bitter perception. [provided by RefSeq, Jul 2008]","start":141778442,"end":141780819,"strand":1,"description":"taste 2 receptor member 4 [Source:HGNC Symbol;Acc:HGNC:14911]"}, {"versioned_ensembl_gene_id":"ENSG00000119737.5","gene_symbol":"GPR75","gene_name":"G protein-coupled receptor 75 [Source:HGNC Symbol;Acc:HGNC:4526]","synonyms":"WI-31133","biotype":"protein_coding","ncbi_id":"10936","summary":"GPR75 is a member of the G protein-coupled receptor family. GPRs are cell surface receptors that activate guanine-nucleotide binding proteins upon the binding of a ligand.[supplied by OMIM, Jul 2002]","start":53852913,"end":53859989,"strand":-1,"description":"G protein-coupled receptor 75 [Source:HGNC Symbol;Acc:HGNC:4526]"}, {"versioned_ensembl_gene_id":"ENSG00000275544.4","gene_symbol":"BDH1","gene_name":"3-hydroxybutyrate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:1027]","synonyms":"SDR9C1,BDH","biotype":"protein_coding","ncbi_id":"622","summary":"This gene encodes a member of the short-chain dehydrogenase/reductase gene family. The encoded protein forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific requirement for phosphatidylcholine for optimal enzymatic activity. The encoded protein catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the two major ketone bodies produced during fatty acid catabolism. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]","start":197506664,"end":197557450,"strand":-1,"description":"3-hydroxybutyrate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:1027]"}, {"versioned_ensembl_gene_id":"ENSG00000280250.1","gene_symbol":"AC097372.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":146231892,"end":146232267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162592.9","gene_symbol":"CCDC27","gene_name":"coiled-coil domain containing 27 [Source:HGNC Symbol;Acc:HGNC:26546]","synonyms":"FLJ32825","biotype":"protein_coding","ncbi_id":"148870","summary":null,"start":3746460,"end":3771645,"strand":1,"description":"coiled-coil domain containing 27 [Source:HGNC Symbol;Acc:HGNC:26546]"}, {"versioned_ensembl_gene_id":"ENSG00000243570.9","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":32022093,"end":32028527,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000279845.1","gene_symbol":"AC097372.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":146180851,"end":146181316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265241.6","gene_symbol":"RBM8A","gene_name":"RNA binding motif protein 8A [Source:HGNC Symbol;Acc:HGNC:9905]","synonyms":"RBM8,BOV-1C,BOV-1B,BOV-1A,ZNRP,Y14,RBM8B","biotype":"protein_coding","ncbi_id":"9939","summary":"This gene encodes a protein with a conserved RNA-binding motif. The protein is found predominantly in the nucleus, although it is also present in the cytoplasm. It is preferentially associated with mRNAs produced by splicing, including both nuclear mRNAs and newly exported cytoplasmic mRNAs. It is thought that the protein remains associated with spliced mRNAs as a tag to indicate where introns had been present, thus coupling pre- and post-mRNA splicing events. Previously, it was thought that two genes encode this protein, RBM8A and RBM8B; it is now thought that the RBM8B locus is a pseudogene. There are two alternate translation start codons with this gene, which result in two forms of the protein. An allele mutation and a low-frequency noncoding single-nucleotide polymorphism (SNP) in this gene cause thrombocytopenia-absent radius (TAR) syndrome. [provided by RefSeq, Jul 2013]","start":145917714,"end":145927678,"strand":-1,"description":"RNA binding motif protein 8A [Source:HGNC Symbol;Acc:HGNC:9905]"}, {"versioned_ensembl_gene_id":"ENSG00000243415.2","gene_symbol":"AC107021.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":146064042,"end":146105204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261075.1","gene_symbol":"LINC01195","gene_name":"long intergenic non-protein coding RNA 1195 [Source:HGNC Symbol;Acc:HGNC:49550]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266959","summary":null,"start":9446010,"end":9455505,"strand":-1,"description":"long intergenic non-protein coding RNA 1195 [Source:HGNC Symbol;Acc:HGNC:49550]"}, {"versioned_ensembl_gene_id":"ENSG00000278431.1","gene_symbol":"AC243547.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145961388,"end":145964422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249266.1","gene_symbol":"MTHFD2P6","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130042","summary":null,"start":41967139,"end":41968366,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48864]"}, {"versioned_ensembl_gene_id":"ENSG00000238029.1","gene_symbol":"AC012493.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100425348,"end":100426107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271346.1","gene_symbol":"AC008162.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120876552,"end":120876805,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239694.1","gene_symbol":"RPSAP38","gene_name":"ribosomal protein SA pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35963]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130676","summary":null,"start":41951313,"end":41952193,"strand":-1,"description":"ribosomal protein SA pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35963]"}, {"versioned_ensembl_gene_id":"ENSG00000222001.2","gene_symbol":"AC106876.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":233012614,"end":233015885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181511.5","gene_symbol":"AC011890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120733094,"end":120733396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197376.3","gene_symbol":"AC089987.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":48507354,"end":48529897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225170.2","gene_symbol":"AL049737.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22272052,"end":22273454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234862.1","gene_symbol":"AL035258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22220554,"end":22223283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121749.15","gene_symbol":"TBC1D15","gene_name":"TBC1 domain family member 15 [Source:HGNC Symbol;Acc:HGNC:25694]","synonyms":"FLJ12085,DKFZp761D0223","biotype":"protein_coding","ncbi_id":"64786","summary":"This gene encodes a member of the Ras-like proteins in brain-GTPase activating protein superfamily that share a conserved Tre-2/Bub2/Cdc16 domain. The encoded protein interacts with Ras-like protein in brain 5A and may function as a regulator of intracellular trafficking. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":71839707,"end":71927248,"strand":1,"description":"TBC1 domain family member 15 [Source:HGNC Symbol;Acc:HGNC:25694]"}, {"versioned_ensembl_gene_id":"ENSG00000275949.5","gene_symbol":"AC139677.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":46812294,"end":46875243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234435.2","gene_symbol":"LINC01432","gene_name":"long intergenic non-protein coding RNA 1432 [Source:HGNC Symbol;Acc:HGNC:50745]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100270679","summary":null,"start":22054090,"end":22074654,"strand":1,"description":"long intergenic non-protein coding RNA 1432 [Source:HGNC Symbol;Acc:HGNC:50745]"}, {"versioned_ensembl_gene_id":"ENSG00000068001.13","gene_symbol":"HYAL2","gene_name":"hyaluronoglucosaminidase 2 [Source:HGNC Symbol;Acc:HGNC:5321]","synonyms":"LUCA2,LuCa-2","biotype":"protein_coding","ncbi_id":"8692","summary":"This gene encodes a weak acid-active hyaluronidase. The encoded protein is similar in structure to other more active hyaluronidases. Hyaluronidases degrade hyaluronan, one of the major glycosaminoglycans of the extracellular matrix. Hyaluronan and fragments of hyaluronan are thought to be involved in cell proliferation, migration and differentiation. Although it was previously thought to be a lysosomal hyaluronidase that is active at a pH below 4, the encoded protein is likely a GPI-anchored cell surface protein. This hyaluronidase serves as a receptor for the oncogenic virus Jaagsiekte sheep retrovirus. The gene is one of several related genes in a region of chromosome 3p21.3 associated with tumor suppression. This gene encodes two alternatively spliced transcript variants which differ only in the 5' UTR.[provided by RefSeq, Mar 2010]","start":50317790,"end":50322906,"strand":-1,"description":"hyaluronoglucosaminidase 2 [Source:HGNC Symbol;Acc:HGNC:5321]"}, {"versioned_ensembl_gene_id":"ENSG00000284221.1","gene_symbol":"AC099654.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57192405,"end":57192698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284098.1","gene_symbol":"AC099654.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57190300,"end":57190460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259970.1","gene_symbol":"AC099668.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":49684480,"end":49684983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255478.1","gene_symbol":"AP000944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65367438,"end":65375299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260671.2","gene_symbol":"AC010536.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87739771,"end":87747706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269935.1","gene_symbol":"AC092720.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87600526,"end":87602190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184208.10","gene_symbol":"C22orf46","gene_name":"chromosome 22 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:26294]","synonyms":"FLJ23584,CTA-216E10.6","biotype":"protein_coding","ncbi_id":"79640","summary":null,"start":41688939,"end":41698136,"strand":1,"description":"chromosome 22 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:26294]"}, {"versioned_ensembl_gene_id":"ENSG00000254712.1","gene_symbol":"AC087280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6843664,"end":6844666,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272505.1","gene_symbol":"AC104964.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10486807,"end":10489666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281019.1","gene_symbol":"AC116351.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":987180,"end":997308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236155.6","gene_symbol":"AL355877.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26209741,"end":26229840,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263042.5","gene_symbol":"WEE2","gene_name":"WEE1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:19684]","synonyms":"FLJ16107","biotype":"protein_coding","ncbi_id":"494551","summary":null,"start":141714361,"end":141737279,"strand":1,"description":"WEE1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:19684]"}, {"versioned_ensembl_gene_id":"ENSG00000127980.15","gene_symbol":"PEX1","gene_name":"peroxisomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8850]","synonyms":"ZWS1,ZWS","biotype":"protein_coding","ncbi_id":"5189","summary":"This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]","start":92487020,"end":92528531,"strand":-1,"description":"peroxisomal biogenesis factor 1 [Source:HGNC Symbol;Acc:HGNC:8850]"}, {"versioned_ensembl_gene_id":"ENSG00000276875.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54838897,"end":54850914,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000248347.3","gene_symbol":"AC120036.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":47089572,"end":47198861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261465.6","gene_symbol":"AC099518.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19062499,"end":19067691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102158.19","gene_symbol":"MAGT1","gene_name":"magnesium transporter 1 [Source:HGNC Symbol;Acc:HGNC:28880]","synonyms":"MRX95,IAP,DKFZp564K142,OST3B","biotype":"protein_coding","ncbi_id":"84061","summary":"This gene encodes a ubiquitously expressed magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause a form of X-linked intellectual disability (XLID). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jul 2017]","start":77826364,"end":77895593,"strand":-1,"description":"magnesium transporter 1 [Source:HGNC Symbol;Acc:HGNC:28880]"}, {"versioned_ensembl_gene_id":"ENSG00000022567.9","gene_symbol":"SLC45A4","gene_name":"solute carrier family 45 member 4 [Source:HGNC Symbol;Acc:HGNC:29196]","synonyms":"KIAA1126","biotype":"protein_coding","ncbi_id":"57210","summary":null,"start":141207166,"end":141308305,"strand":-1,"description":"solute carrier family 45 member 4 [Source:HGNC Symbol;Acc:HGNC:29196]"}, {"versioned_ensembl_gene_id":"ENSG00000254244.1","gene_symbol":"PAICSP4","gene_name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38097]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"780813","summary":null,"start":4787332,"end":4788584,"strand":1,"description":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38097]"}, {"versioned_ensembl_gene_id":"ENSG00000235411.1","gene_symbol":"AC007041.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20239892,"end":20241046,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282197.1","gene_symbol":"IGHVII-1-1","gene_name":"immunoglobulin heavy variable (II)-1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5670]","synonyms":"IGHV(II)-1-1","biotype":"IG_V_pseudogene","ncbi_id":"28377","summary":null,"start":105945981,"end":105946160,"strand":-1,"description":"immunoglobulin heavy variable (II)-1-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5670]"}, {"versioned_ensembl_gene_id":"ENSG00000224117.1","gene_symbol":"PTPN2P2","gene_name":"protein tyrosine phosphatase, non-receptor type 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646758","summary":null,"start":30553670,"end":30554693,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9654]"}, {"versioned_ensembl_gene_id":"ENSG00000249092.1","gene_symbol":"AC008945.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42892319,"end":42892817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124508.16","gene_symbol":"BTN2A2","gene_name":"butyrophilin subfamily 2 member A2 [Source:HGNC Symbol;Acc:HGNC:1137]","synonyms":"BTN2.2,BTF2,BT2.2","biotype":"protein_coding","ncbi_id":"10385","summary":"Butyrophilin is the major protein associated with fat droplets in the milk. This gene is a member of the BTN2 subfamily of genes, which encode proteins belonging to the butyrophilin protein family. The gene is located in a cluster on chromosome 6, consisting of seven genes belonging to the expanding B7/butyrophilin-like group, a subset of the immunoglobulin gene superfamily. The encoded protein is a type I receptor glycoprotein involved in lipid, fatty-acid and sterol metabolism. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":26383096,"end":26394874,"strand":1,"description":"butyrophilin subfamily 2 member A2 [Source:HGNC Symbol;Acc:HGNC:1137]"}, {"versioned_ensembl_gene_id":"ENSG00000262777.1","gene_symbol":"AC032044.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1424473,"end":1426484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232119.7","gene_symbol":"MCTS1","gene_name":"MCTS1, re-initiation and release factor [Source:HGNC Symbol;Acc:HGNC:23357]","synonyms":"MCT-1","biotype":"protein_coding","ncbi_id":"28985","summary":null,"start":120594010,"end":120621074,"strand":1,"description":"MCTS1, re-initiation and release factor [Source:HGNC Symbol;Acc:HGNC:23357]"}, {"versioned_ensembl_gene_id":"ENSG00000231731.7","gene_symbol":"AC010976.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":127455394,"end":127514623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205583.13","gene_symbol":"STAG3L1","gene_name":"stromal antigen 3-like 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33852]","synonyms":"STAG3L1P,DKFZP434A0131","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54441","summary":null,"start":75359194,"end":75395383,"strand":1,"description":"stromal antigen 3-like 1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:33852]"}, {"versioned_ensembl_gene_id":"ENSG00000138315.12","gene_symbol":"OIT3","gene_name":"oncoprotein induced transcript 3 [Source:HGNC Symbol;Acc:HGNC:29953]","synonyms":"LZP,FLJ39116","biotype":"protein_coding","ncbi_id":"170392","summary":"This gene was identified due to its downregulation in hepatocarcinomas. The encoded protein may be involved in liver development and function. [provided by RefSeq, Sep 2016]","start":72893581,"end":72933033,"strand":1,"description":"oncoprotein induced transcript 3 [Source:HGNC Symbol;Acc:HGNC:29953]"}, {"versioned_ensembl_gene_id":"ENSG00000215506.5","gene_symbol":"TPTE2P4","gene_name":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38077]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"286573","summary":null,"start":26508213,"end":26579690,"strand":1,"description":"transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38077]"}, {"versioned_ensembl_gene_id":"ENSG00000114378.16","gene_symbol":"HYAL1","gene_name":"hyaluronoglucosaminidase 1 [Source:HGNC Symbol;Acc:HGNC:5320]","synonyms":"NAT6,LUCA1,HYAL-1,FUS2","biotype":"protein_coding","ncbi_id":"3373","summary":"This gene encodes a lysosomal hyaluronidase. Hyaluronidases intracellularly degrade hyaluronan, one of the major glycosaminoglycans of the extracellular matrix. Hyaluronan is thought to be involved in cell proliferation, migration and differentiation. This enzyme is active at an acidic pH and is the major hyaluronidase in plasma. Mutations in this gene are associated with mucopolysaccharidosis type IX, or hyaluronidase deficiency. The gene is one of several related genes in a region of chromosome 3p21.3 associated with tumor suppression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":50299889,"end":50312381,"strand":-1,"description":"hyaluronoglucosaminidase 1 [Source:HGNC Symbol;Acc:HGNC:5320]"}, {"versioned_ensembl_gene_id":"ENSG00000253782.1","gene_symbol":"AC091163.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46930840,"end":46934446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115657.12","gene_symbol":"ABCB6","gene_name":"ATP binding cassette subfamily B member 6 (Langereis blood group) [Source:HGNC Symbol;Acc:HGNC:47]","synonyms":"MTABC3,EST45597,umat","biotype":"protein_coding","ncbi_id":"10058","summary":"This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. This protein is a member of the heavy metal importer subfamily and plays a role in porphyrin transport. This gene is the molecular basis of the Langereis (Lan) blood group antigen and mutations in this gene underlie familial pseudohyperkalemia and dyschromatosis universalis hereditaria. [provided by RefSeq, Mar 2017]","start":219209768,"end":219218990,"strand":-1,"description":"ATP binding cassette subfamily B member 6 (Langereis blood group) [Source:HGNC Symbol;Acc:HGNC:47]"}, {"versioned_ensembl_gene_id":"ENSG00000159055.3","gene_symbol":"MIS18A","gene_name":"MIS18 kinetochore protein A [Source:HGNC Symbol;Acc:HGNC:1286]","synonyms":"hMis18alpha,FASP1,C21orf46,C21orf45,B28","biotype":"protein_coding","ncbi_id":"54069","summary":null,"start":32268219,"end":32279069,"strand":-1,"description":"MIS18 kinetochore protein A [Source:HGNC Symbol;Acc:HGNC:1286]"}, {"versioned_ensembl_gene_id":"ENSG00000274044.4","gene_symbol":"LINC01660","gene_name":"long intergenic non-protein coding RNA 1660 [Source:HGNC Symbol;Acc:HGNC:52448]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729461","summary":null,"start":18361823,"end":18391105,"strand":-1,"description":"long intergenic non-protein coding RNA 1660 [Source:HGNC Symbol;Acc:HGNC:52448]"}, {"versioned_ensembl_gene_id":"ENSG00000227256.1","gene_symbol":"MIS18A-AS1","gene_name":"MIS18A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40106]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874202","summary":null,"start":32277863,"end":32280988,"strand":1,"description":"MIS18A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40106]"}, {"versioned_ensembl_gene_id":"ENSG00000206384.10","gene_symbol":"COL6A6","gene_name":"collagen type VI alpha 6 chain [Source:HGNC Symbol;Acc:HGNC:27023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"131873","summary":"This gene encodes a large protein that contains multiple von Willebrand factor domains and forms a component of the basal lamina of epithelial cells. This protein may regulate epithelial cell-fibronectin interactions. Variation in this gene may be implicated in skin diseases. [provided by RefSeq, May 2017]","start":130560334,"end":130678155,"strand":1,"description":"collagen type VI alpha 6 chain [Source:HGNC Symbol;Acc:HGNC:27023]"}, {"versioned_ensembl_gene_id":"ENSG00000280578.1","gene_symbol":"AC226496.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68766262,"end":68766817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065000.15","gene_symbol":"AP3D1","gene_name":"adaptor related protein complex 3 delta 1 subunit [Source:HGNC Symbol;Acc:HGNC:568]","synonyms":"ADTD","biotype":"protein_coding","ncbi_id":"8943","summary":"The protein encoded by this gene is a subunit of the AP3 adaptor-like complex, which is not clathrin-associated, but is associated with the golgi region, as well as more peripheral structures. The AP-3 complex facilitates the budding of vesicles from the golgi membrane, and may be directly involved in trafficking to lysosomes. This subunit is implicated in intracellular biogenesis and trafficking of pigment granules, and possibly platelet dense granules and neurotransmitter vesicles. Defects in this gene are a cause of a new type of Hermansky-Pudlak syndrome. [provided by RefSeq, Feb 2017]","start":2100988,"end":2164465,"strand":-1,"description":"adaptor related protein complex 3 delta 1 subunit [Source:HGNC Symbol;Acc:HGNC:568]"}, {"versioned_ensembl_gene_id":"ENSG00000254154.8","gene_symbol":"AL359075.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":177928788,"end":178038007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147955.16","gene_symbol":"SIGMAR1","gene_name":"sigma non-opioid intracellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:8157]","synonyms":"SR-BP1,OPRS1","biotype":"protein_coding","ncbi_id":"10280","summary":"This gene encodes a receptor protein that interacts with a variety of psychotomimetic drugs, including cocaine and amphetamines. The receptor is believed to play an important role in the cellular functions of various tissues associated with the endocrine, immune, and nervous systems. As indicated by its previous name, opioid receptor sigma 1 (OPRS1), the product of this gene was erroneously thought to function as an opioid receptor; it is now thought to be a non-opioid receptor. Mutations in this gene has been associated with juvenile amyotrophic lateral sclerosis 16. Alternative splicing of this gene results in transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2013]","start":34634722,"end":34637809,"strand":-1,"description":"sigma non-opioid intracellular receptor 1 [Source:HGNC Symbol;Acc:HGNC:8157]"}, {"versioned_ensembl_gene_id":"ENSG00000237053.1","gene_symbol":"FUCA1P1","gene_name":"fucosidase, alpha-L- 1, tissue pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4007]","synonyms":"FUCA1P","biotype":"processed_pseudogene","ncbi_id":"2518","summary":null,"start":176804987,"end":176806337,"strand":-1,"description":"fucosidase, alpha-L- 1, tissue pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4007]"}, {"versioned_ensembl_gene_id":"ENSG00000277101.4","gene_symbol":"ARHGEF26","gene_name":"Rho guanine nucleotide exchange factor 26 [Source:HGNC Symbol;Acc:HGNC:24490]","synonyms":"SGEF,DKFZP434D146","biotype":"protein_coding","ncbi_id":"26084","summary":"This gene encodes a member of the Rho-guanine nucleotide exchange factor (Rho-GEF) family. These proteins regulate Rho GTPases by catalyzing the exchange of GDP for GTP. The encoded protein specifically activates RhoG and plays a role in the promotion of macropinocytosis. Underexpression of the encoded protein may be a predictive marker of chemoresistant disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":154121003,"end":154261004,"strand":1,"description":"Rho guanine nucleotide exchange factor 26 [Source:HGNC Symbol;Acc:HGNC:24490]"}, {"versioned_ensembl_gene_id":"ENSG00000258843.1","gene_symbol":"AL133485.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50821880,"end":50823501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170289.12","gene_symbol":"CNGB3","gene_name":"cyclic nucleotide gated channel beta 3 [Source:HGNC Symbol;Acc:HGNC:2153]","synonyms":"RMCH,ACHM3,ACHM1","biotype":"protein_coding","ncbi_id":"54714","summary":"This gene encodes the beta subunit of a cyclic nucleotide-gated ion channel. The encoded beta subunit appears to play a role in modulation of channel function in cone photoreceptors. This heterotetrameric channel is necessary for sensory transduction, and mutations in this gene have been associated with achromatopsia 3, progressive cone dystrophy, and juvenile macular degeneration, also known as Stargardt Disease. [provided by RefSeq, Feb 2010]","start":86553977,"end":86743675,"strand":-1,"description":"cyclic nucleotide gated channel beta 3 [Source:HGNC Symbol;Acc:HGNC:2153]"}, {"versioned_ensembl_gene_id":"ENSG00000205333.5","gene_symbol":"GOLGA2P1","gene_name":"golgin A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31052]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418751","summary":null,"start":86657388,"end":86660293,"strand":-1,"description":"golgin A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31052]"}, {"versioned_ensembl_gene_id":"ENSG00000253292.1","gene_symbol":"MIOXP1","gene_name":"myo-inositol oxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50748]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419614","summary":null,"start":86593755,"end":86594589,"strand":-1,"description":"myo-inositol oxygenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50748]"}, {"versioned_ensembl_gene_id":"ENSG00000275835.4","gene_symbol":"TUBGCP5","gene_name":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]","synonyms":"KIAA1899,GCP5","biotype":"protein_coding","ncbi_id":"114791","summary":null,"start":22983192,"end":23039673,"strand":-1,"description":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]"}, {"versioned_ensembl_gene_id":"ENSG00000232030.3","gene_symbol":"MAGEB6P1","gene_name":"MAGE family member B6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28824]","synonyms":"MAGEB6B","biotype":"protein_coding","ncbi_id":"392433","summary":null,"start":26160601,"end":26161824,"strand":1,"description":"MAGE family member B6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28824]"}, {"versioned_ensembl_gene_id":"ENSG00000135517.6","gene_symbol":"MIP","gene_name":"major intrinsic protein of lens fiber [Source:HGNC Symbol;Acc:HGNC:7103]","synonyms":"MP26,LIM1,AQP0","biotype":"protein_coding","ncbi_id":"4284","summary":"Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13. [provided by RefSeq, Jul 2008]","start":56449502,"end":56469166,"strand":-1,"description":"major intrinsic protein of lens fiber [Source:HGNC Symbol;Acc:HGNC:7103]"}, {"versioned_ensembl_gene_id":"ENSG00000228480.1","gene_symbol":"AC130464.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26354796,"end":26358355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238260.1","gene_symbol":"AL513320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3623190,"end":3624743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273079.5","gene_symbol":"GRIN2B","gene_name":"glutamate ionotropic receptor NMDA type subunit 2B [Source:HGNC Symbol;Acc:HGNC:4586]","synonyms":"NMDAR2B,GluN2B","biotype":"protein_coding","ncbi_id":"2904","summary":"This gene encodes a member of the N-methyl-D-aspartate (NMDA) receptor family within the ionotropic glutamate receptor superfamily. The encoded protein is a subunit of the NMDA receptor ion channel which acts as an agonist binding site for glutamate. The NMDA receptors mediate a slow calcium-permeable component of excitatory synaptic transmission in the central nervous system. The NMDA receptors are heterotetramers of seven genetically encoded, differentially expressed subunits including NR1 (GRIN1), NR2 (GRIN2A, GRIN2B, GRIN2C, or GRIN2D) and NR3 (GRIN3A or GRIN3B). The early expression of this gene in development suggests a role in brain development, circuit formation, synaptic plasticity, and cellular migration and differentiation. Naturally occurring mutations within this gene are associated with neurodevelopmental disorders including autism spectrum disorder, attention deficit hyperactivity disorder, epilepsy, and schizophrenia. [provided by RefSeq, Aug 2017]","start":13437942,"end":13981957,"strand":-1,"description":"glutamate ionotropic receptor NMDA type subunit 2B [Source:HGNC Symbol;Acc:HGNC:4586]"}, {"versioned_ensembl_gene_id":"ENSG00000277935.1","gene_symbol":"AC007527.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13540231,"end":13544540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230764.1","gene_symbol":"MTND1P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42053]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873171","summary":null,"start":57185788,"end":57186202,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42053]"}, {"versioned_ensembl_gene_id":"ENSG00000204993.3","gene_symbol":"AC139712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52570648,"end":52572522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226536.1","gene_symbol":"SETP15","gene_name":"SET pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42934]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100856877","summary":null,"start":15917548,"end":15918631,"strand":1,"description":"SET pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42934]"}, {"versioned_ensembl_gene_id":"ENSG00000170396.7","gene_symbol":"ZNF804A","gene_name":"zinc finger protein 804A [Source:HGNC Symbol;Acc:HGNC:21711]","synonyms":"C2orf10","biotype":"protein_coding","ncbi_id":"91752","summary":"The protein encoded by this gene is a zinc finger binding protein. Polymorphisms in this gene, especially rs1344706, are thought to confer increased susceptibility to schizophrenia, bipolar disorder, and heroin addiciton. [provided by RefSeq, Nov 2015]","start":184598366,"end":184939492,"strand":1,"description":"zinc finger protein 804A [Source:HGNC Symbol;Acc:HGNC:21711]"}, {"versioned_ensembl_gene_id":"ENSG00000229434.1","gene_symbol":"AC017048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176506245,"end":176507702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250995.1","gene_symbol":"AL391280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118769796,"end":118770857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270727.1","gene_symbol":"AL590032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20547171,"end":20547422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274729.1","gene_symbol":"DEFB105B","gene_name":"defensin beta 105B [Source:HGNC Symbol;Acc:HGNC:29930]","synonyms":null,"biotype":"protein_coding","ncbi_id":"504180","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 105, DEFB105A and DEFB105B, in tail-to-tail orientation. This gene, DEFB105B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7479647,"end":7481569,"strand":1,"description":"defensin beta 105B [Source:HGNC Symbol;Acc:HGNC:29930]"}, {"versioned_ensembl_gene_id":"ENSG00000274854.2","gene_symbol":"IGLV1-44","gene_name":"immunoglobulin lambda variable 1-44 [Source:HGNC Symbol;Acc:HGNC:5879]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28823","summary":null,"start":22380766,"end":22381346,"strand":1,"description":"immunoglobulin lambda variable 1-44 [Source:HGNC Symbol;Acc:HGNC:5879]"}, {"versioned_ensembl_gene_id":"ENSG00000255158.1","gene_symbol":"AC131934.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":665910,"end":678391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231817.7","gene_symbol":"LINC01198","gene_name":"long intergenic non-protein coding RNA 1198 [Source:HGNC Symbol;Acc:HGNC:49598]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929344","summary":null,"start":46455135,"end":46486506,"strand":-1,"description":"long intergenic non-protein coding RNA 1198 [Source:HGNC Symbol;Acc:HGNC:49598]"}, {"versioned_ensembl_gene_id":"ENSG00000266368.1","gene_symbol":"AC005410.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11953889,"end":11977594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259422.1","gene_symbol":"AC091100.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76174891,"end":76181486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171303.6","gene_symbol":"KCNK3","gene_name":"potassium two pore domain channel subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:6278]","synonyms":"TASK-1,TASK,K2p3.1","biotype":"protein_coding","ncbi_id":"3777","summary":"This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene. [provided by RefSeq, Aug 2008]","start":26692690,"end":26733420,"strand":1,"description":"potassium two pore domain channel subfamily K member 3 [Source:HGNC Symbol;Acc:HGNC:6278]"}, {"versioned_ensembl_gene_id":"ENSG00000172830.12","gene_symbol":"SSH3","gene_name":"slingshot protein phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:30581]","synonyms":"FLJ20515,FLJ10928","biotype":"protein_coding","ncbi_id":"54961","summary":"The ADF (actin-depolymerizing factor)/cofilin family (see MIM 601442) is composed of stimulus-responsive mediators of actin dynamics. ADF/cofilin proteins are inactivated by kinases such as LIM domain kinase-1 (LIMK1; MIM 601329). The SSH family appears to play a role in actin dynamics by reactivating ADF/cofilin proteins in vivo (Niwa et al., 2002 [PubMed 11832213]).[supplied by OMIM, Mar 2008]","start":67303448,"end":67312607,"strand":1,"description":"slingshot protein phosphatase 3 [Source:HGNC Symbol;Acc:HGNC:30581]"}, {"versioned_ensembl_gene_id":"ENSG00000225012.5","gene_symbol":"AL121872.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89423738,"end":89446983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250934.1","gene_symbol":"AC016924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126266796,"end":126291279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282346.1","gene_symbol":"IGHD5-18","gene_name":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]","synonyms":"IGHD518","biotype":"IG_D_gene","ncbi_id":"28490","summary":null,"start":105894313,"end":105894332,"strand":-1,"description":"immunoglobulin heavy diversity 5-18 [Source:HGNC Symbol;Acc:HGNC:5509]"}, {"versioned_ensembl_gene_id":"ENSG00000230323.5","gene_symbol":"LINC00159","gene_name":"long intergenic non-protein coding RNA 159 [Source:HGNC Symbol;Acc:HGNC:1285]","synonyms":"NCRNA00159,C21orf44","biotype":"lincRNA","ncbi_id":"100551499","summary":null,"start":32080316,"end":32197813,"strand":-1,"description":"long intergenic non-protein coding RNA 159 [Source:HGNC Symbol;Acc:HGNC:1285]"}, {"versioned_ensembl_gene_id":"ENSG00000281890.1","gene_symbol":"AC226496.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68760003,"end":68762508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280720.1","gene_symbol":"AC226496.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68716590,"end":68716745,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000040199.18","gene_symbol":"PHLPP2","gene_name":"PH domain and leucine rich repeat protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:29149]","synonyms":"PHLPPL,KIAA0931,PPM3B","biotype":"protein_coding","ncbi_id":"23035","summary":null,"start":71637835,"end":71724701,"strand":-1,"description":"PH domain and leucine rich repeat protein phosphatase 2 [Source:HGNC Symbol;Acc:HGNC:29149]"}, {"versioned_ensembl_gene_id":"ENSG00000281763.2","gene_symbol":"DHX36","gene_name":"DEAH-box helicase 36 [Source:HGNC Symbol;Acc:HGNC:14410]","synonyms":"MLEL1,KIAA1488,DDX36","biotype":"protein_coding","ncbi_id":"170506","summary":"This gene is a member of the DEAH-box family of RNA-dependent NTPases which are named after the conserved amino acid sequence Asp-Glu-Ala-His in motif II. The protein encoded by this gene has been shown to enhance the deadenylation and decay of mRNAs with 3'-UTR AU-rich elements (ARE-mRNA). The protein has also been shown to resolve into single strands the highly stable tetramolecular DNA configuration (G4) that can form spontaneously in guanine-rich regions of DNA. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":154275723,"end":154284039,"strand":-1,"description":"DEAH-box helicase 36 [Source:HGNC Symbol;Acc:HGNC:14410]"}, {"versioned_ensembl_gene_id":"ENSG00000233756.5","gene_symbol":"DSCAM-IT1","gene_name":"DSCAM intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41327]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874326","summary":null,"start":40615378,"end":40630767,"strand":-1,"description":"DSCAM intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41327]"}, {"versioned_ensembl_gene_id":"ENSG00000248213.3","gene_symbol":"CICP16","gene_name":"capicua transcriptional repressor pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38550]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420203","summary":null,"start":118635970,"end":118638782,"strand":-1,"description":"capicua transcriptional repressor pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38550]"}, {"versioned_ensembl_gene_id":"ENSG00000238190.1","gene_symbol":"HMGB1P15","gene_name":"high mobility group box 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39097]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644129","summary":null,"start":50931114,"end":50931548,"strand":-1,"description":"high mobility group box 1 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:39097]"}, {"versioned_ensembl_gene_id":"ENSG00000164124.10","gene_symbol":"TMEM144","gene_name":"transmembrane protein 144 [Source:HGNC Symbol;Acc:HGNC:25633]","synonyms":"FLJ11155","biotype":"protein_coding","ncbi_id":"55314","summary":null,"start":158201604,"end":158255411,"strand":1,"description":"transmembrane protein 144 [Source:HGNC Symbol;Acc:HGNC:25633]"}, {"versioned_ensembl_gene_id":"ENSG00000248472.8","gene_symbol":"DDX11L9","gene_name":"DEAD/H-box helicase 11 like 9 [Source:HGNC Symbol;Acc:HGNC:37109]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288486","summary":null,"start":101976558,"end":101979093,"strand":-1,"description":"DEAD/H-box helicase 11 like 9 [Source:HGNC Symbol;Acc:HGNC:37109]"}, {"versioned_ensembl_gene_id":"ENSG00000233621.1","gene_symbol":"LINC01137","gene_name":"long intergenic non-protein coding RNA 1137 [Source:HGNC Symbol;Acc:HGNC:49453]","synonyms":"LOC728431","biotype":"antisense_RNA","ncbi_id":"728431","summary":null,"start":37454879,"end":37474411,"strand":-1,"description":"long intergenic non-protein coding RNA 1137 [Source:HGNC Symbol;Acc:HGNC:49453]"}, {"versioned_ensembl_gene_id":"ENSG00000232736.1","gene_symbol":"AC007551.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35768122,"end":35768640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278041.1","gene_symbol":"AL133325.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21499261,"end":21502934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238246.1","gene_symbol":"AC069549.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20070805,"end":20091784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277802.2","gene_symbol":"AF252830.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7332922,"end":7334514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238215.1","gene_symbol":"AL513185.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72643011,"end":72644650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102893.15","gene_symbol":"PHKB","gene_name":"phosphorylase kinase regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:8927]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5257","summary":"Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, encoded by this gene, which is a member of the phosphorylase b kinase regulatory subunit family. The gamma subunit also includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9B, also known as phosphorylase kinase deficiency of liver and muscle. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. Two pseudogenes have been found on chromosomes 14 and 20, respectively.[provided by RefSeq, Feb 2010]","start":47461123,"end":47701523,"strand":1,"description":"phosphorylase kinase regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:8927]"}, {"versioned_ensembl_gene_id":"ENSG00000248668.2","gene_symbol":"OXCT1-AS1","gene_name":"OXCT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40423]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874002","summary":null,"start":41870030,"end":41872241,"strand":1,"description":"OXCT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40423]"}, {"versioned_ensembl_gene_id":"ENSG00000163873.9","gene_symbol":"GRIK3","gene_name":"glutamate ionotropic receptor kainate type subunit 3 [Source:HGNC Symbol;Acc:HGNC:4581]","synonyms":"GLUR7,GluK3","biotype":"protein_coding","ncbi_id":"2899","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. It is not certain if the subunit encoded by this gene is subject to RNA editing as the other 2 family members (GRIK1 and GRIK2). A Ser310Ala polymorphism has been associated with schizophrenia, and there are conflicting reports of its association with the pathogenesis of delirium tremens in alcoholics. [provided by RefSeq, Jul 2008]","start":36795527,"end":37034129,"strand":-1,"description":"glutamate ionotropic receptor kainate type subunit 3 [Source:HGNC Symbol;Acc:HGNC:4581]"}, {"versioned_ensembl_gene_id":"ENSG00000204392.10","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"G7b,C6orf28,YBL026W","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31797396,"end":31806984,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000259918.1","gene_symbol":"NDUFA5P11","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48853]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724866","summary":null,"start":47598654,"end":47598996,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:48853]"}, {"versioned_ensembl_gene_id":"ENSG00000259530.1","gene_symbol":"AC104574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61598514,"end":61605241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232846.1","gene_symbol":"SLC25A6P3","gene_name":"solute carrier family 25 member 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422686","summary":null,"start":51709062,"end":51709940,"strand":1,"description":"solute carrier family 25 member 6 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43852]"}, {"versioned_ensembl_gene_id":"ENSG00000164061.4","gene_symbol":"BSN","gene_name":"bassoon presynaptic cytomatrix protein [Source:HGNC Symbol;Acc:HGNC:1117]","synonyms":"ZNF231","biotype":"protein_coding","ncbi_id":"8927","summary":"Neurotransmitters are released from a specific site in the axon terminal called the active zone, which is composed of synaptic vesicles and a meshwork of cytoskeleton underlying the plasma membrane. The protein encoded by this gene is thought to be a scaffolding protein involved in organizing the presynaptic cytoskeleton. The gene is expressed primarily in neurons in the brain. A similar gene product in rodents is concentrated in the active zone of axon terminals and tightly associated with cytoskeletal structures, and is essential for regulating neurotransmitter release from a subset of synapses. [provided by RefSeq, Jul 2008]","start":49554489,"end":49671545,"strand":1,"description":"bassoon presynaptic cytomatrix protein [Source:HGNC Symbol;Acc:HGNC:1117]"}, {"versioned_ensembl_gene_id":"ENSG00000254746.5","gene_symbol":"AC103855.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45489689,"end":45542474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258234.1","gene_symbol":"AC024257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48231098,"end":48284210,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270446.1","gene_symbol":"AL136363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87806433,"end":87806769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237171.1","gene_symbol":"AC005297.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26223903,"end":26224658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204669.9","gene_symbol":"C9orf57","gene_name":"chromosome 9 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:27037]","synonyms":null,"biotype":"protein_coding","ncbi_id":"138240","summary":null,"start":72051376,"end":72072721,"strand":-1,"description":"chromosome 9 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:27037]"}, {"versioned_ensembl_gene_id":"ENSG00000272234.1","gene_symbol":"AC008945.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42806394,"end":42806997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259397.3","gene_symbol":"AC021231.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35092481,"end":35093210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235194.8","gene_symbol":"PPP1R3E","gene_name":"protein phosphatase 1 regulatory subunit 3E [Source:HGNC Symbol;Acc:HGNC:14943]","synonyms":"FLJ00089","biotype":"protein_coding","ncbi_id":"90673","summary":null,"start":23295643,"end":23302848,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 3E [Source:HGNC Symbol;Acc:HGNC:14943]"}, {"versioned_ensembl_gene_id":"ENSG00000256039.1","gene_symbol":"LINC02446","gene_name":"long intergenic non-protein coding RNA 2446 [Source:HGNC Symbol;Acc:HGNC:53378]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060038","summary":null,"start":10553363,"end":10558049,"strand":1,"description":"long intergenic non-protein coding RNA 2446 [Source:HGNC Symbol;Acc:HGNC:53378]"}, {"versioned_ensembl_gene_id":"ENSG00000258643.5","gene_symbol":"BCL2L2-PABPN1","gene_name":"BCL2L2-PABPN1 readthrough [Source:HGNC Symbol;Acc:HGNC:42959]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529063","summary":"This locus represents naturally occurring read-through transcription between the neighboring BCL2L2 (BCL2-like 2) and PABPN1 (poly(A) binding protein, nuclear 1) genes on chromosome 14. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010]","start":23306835,"end":23325369,"strand":1,"description":"BCL2L2-PABPN1 readthrough [Source:HGNC Symbol;Acc:HGNC:42959]"}, {"versioned_ensembl_gene_id":"ENSG00000261997.1","gene_symbol":"AC007336.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55538200,"end":55542027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249275.1","gene_symbol":"AC093817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157637687,"end":157667044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132514.13","gene_symbol":"CLEC10A","gene_name":"C-type lectin domain containing 10A [Source:HGNC Symbol;Acc:HGNC:16916]","synonyms":"HML,CLECSF14,CLECSF13,CD301,HML2","biotype":"protein_coding","ncbi_id":"10462","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell surface antigen. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":7074537,"end":7080307,"strand":-1,"description":"C-type lectin domain containing 10A [Source:HGNC Symbol;Acc:HGNC:16916]"}, {"versioned_ensembl_gene_id":"ENSG00000260930.1","gene_symbol":"LINC01416","gene_name":"long intergenic non-protein coding RNA 1416 [Source:HGNC Symbol;Acc:HGNC:51645]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927273","summary":null,"start":55881688,"end":55920199,"strand":-1,"description":"long intergenic non-protein coding RNA 1416 [Source:HGNC Symbol;Acc:HGNC:51645]"}, {"versioned_ensembl_gene_id":"ENSG00000196792.11","gene_symbol":"STRN3","gene_name":"striatin 3 [Source:HGNC Symbol;Acc:HGNC:15720]","synonyms":"SG2NA,S/G2NA,PPP2R6B","biotype":"protein_coding","ncbi_id":"29966","summary":null,"start":30893799,"end":31026401,"strand":-1,"description":"striatin 3 [Source:HGNC Symbol;Acc:HGNC:15720]"}, {"versioned_ensembl_gene_id":"ENSG00000258886.2","gene_symbol":"HIGD1AP17","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:43012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874477","summary":null,"start":30964347,"end":30964622,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:43012]"}, {"versioned_ensembl_gene_id":"ENSG00000282545.1","gene_symbol":"RPL5P32","gene_name":"ribosomal protein L5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271207","summary":null,"start":27895704,"end":27896582,"strand":1,"description":"ribosomal protein L5 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36973]"}, {"versioned_ensembl_gene_id":"ENSG00000267712.5","gene_symbol":"LINC01539","gene_name":"long intergenic non-protein coding RNA 1539 [Source:HGNC Symbol;Acc:HGNC:51307]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505474","summary":null,"start":56083356,"end":56137536,"strand":-1,"description":"long intergenic non-protein coding RNA 1539 [Source:HGNC Symbol;Acc:HGNC:51307]"}, {"versioned_ensembl_gene_id":"ENSG00000277361.2","gene_symbol":"OCA2","gene_name":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]","synonyms":"EYCL,D15S12,BEY2,BEY1,BEY,P,EYCL3,EYCL2","biotype":"protein_coding","ncbi_id":"4948","summary":"This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":27871154,"end":28099370,"strand":-1,"description":"OCA2 melanosomal transmembrane protein [Source:HGNC Symbol;Acc:HGNC:8101]"}, {"versioned_ensembl_gene_id":"ENSG00000281783.1","gene_symbol":"FAM99B","gene_name":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]","synonyms":"DKFZp781M09150","biotype":"antisense_RNA","ncbi_id":"100132464","summary":null,"start":1688979,"end":1691339,"strand":-1,"description":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]"}, {"versioned_ensembl_gene_id":"ENSG00000281240.1","gene_symbol":"AP006285.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1694007,"end":1694766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277746.1","gene_symbol":"AC108706.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86816740,"end":86817036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239767.1","gene_symbol":"AC108733.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86264555,"end":86267361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226363.3","gene_symbol":"HAGLROS","gene_name":"HAGLR opposite strand (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50646]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102800310","summary":null,"start":176177717,"end":176179008,"strand":1,"description":"HAGLR opposite strand (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50646]"}, {"versioned_ensembl_gene_id":"ENSG00000224177.6","gene_symbol":"LINC00570","gene_name":"long intergenic non-protein coding RNA 570 [Source:HGNC Symbol;Acc:HGNC:43717]","synonyms":"ncRNA-a5","biotype":"lincRNA","ncbi_id":"100874055","summary":null,"start":11393981,"end":11403077,"strand":1,"description":"long intergenic non-protein coding RNA 570 [Source:HGNC Symbol;Acc:HGNC:43717]"}, {"versioned_ensembl_gene_id":"ENSG00000135636.13","gene_symbol":"DYSF","gene_name":"dysferlin [Source:HGNC Symbol;Acc:HGNC:3097]","synonyms":"FER1L1,LGMD2B","biotype":"protein_coding","ncbi_id":"8291","summary":"The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008]","start":71453722,"end":71686768,"strand":1,"description":"dysferlin [Source:HGNC Symbol;Acc:HGNC:3097]"}, {"versioned_ensembl_gene_id":"ENSG00000278476.1","gene_symbol":"AC009414.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36299388,"end":36299830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124222.22","gene_symbol":"STX16","gene_name":"syntaxin 16 [Source:HGNC Symbol;Acc:HGNC:11431]","synonyms":"SYN16,hsyn16","biotype":"protein_coding","ncbi_id":"8675","summary":"This gene encodes a protein that is a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V-SNARES (vesicle-SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this gene. Read-through transcription also exists between this gene and the neighboring downstream aminopeptidase-like 1 (NPEPL1) gene. [provided by RefSeq, Mar 2011]","start":58651253,"end":58679526,"strand":1,"description":"syntaxin 16 [Source:HGNC Symbol;Acc:HGNC:11431]"}, {"versioned_ensembl_gene_id":"ENSG00000230697.1","gene_symbol":"SAP18P3","gene_name":"SAP18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51569]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106660616","summary":null,"start":20007852,"end":20008247,"strand":-1,"description":"SAP18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51569]"}, {"versioned_ensembl_gene_id":"ENSG00000248457.1","gene_symbol":"LINC02220","gene_name":"long intergenic non-protein coding RNA 2220 [Source:HGNC Symbol;Acc:HGNC:53087]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374658","summary":null,"start":12914068,"end":13032886,"strand":-1,"description":"long intergenic non-protein coding RNA 2220 [Source:HGNC Symbol;Acc:HGNC:53087]"}, {"versioned_ensembl_gene_id":"ENSG00000144566.10","gene_symbol":"RAB5A","gene_name":"RAB5A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9783]","synonyms":"RAB5","biotype":"protein_coding","ncbi_id":"5868","summary":null,"start":19947079,"end":19985175,"strand":1,"description":"RAB5A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9783]"}, {"versioned_ensembl_gene_id":"ENSG00000283269.1","gene_symbol":"AC005524.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28683071,"end":28727777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261838.5","gene_symbol":"AC092718.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81069854,"end":81076598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164631.18","gene_symbol":"ZNF12","gene_name":"zinc finger protein 12 [Source:HGNC Symbol;Acc:HGNC:12902]","synonyms":"ZNF325,KOX3,GIOT-3","biotype":"protein_coding","ncbi_id":"7559","summary":"This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with eight C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in developmental control of gene expression. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":6688433,"end":6706923,"strand":-1,"description":"zinc finger protein 12 [Source:HGNC Symbol;Acc:HGNC:12902]"}, {"versioned_ensembl_gene_id":"ENSG00000206366.6","gene_symbol":"ZBTB12","gene_name":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]","synonyms":"NG35,G10,D6S59E,C6orf46","biotype":"protein_coding","ncbi_id":"221527","summary":null,"start":31889987,"end":31892374,"strand":-1,"description":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]"}, {"versioned_ensembl_gene_id":"ENSG00000261141.1","gene_symbol":"AC092718.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81055301,"end":81056426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118007.12","gene_symbol":"STAG1","gene_name":"stromal antigen 1 [Source:HGNC Symbol;Acc:HGNC:11354]","synonyms":"SCC3A,SA1,SA-1","biotype":"protein_coding","ncbi_id":"10274","summary":"This gene is a member of the SCC3 family and is expressed in the nucleus. It encodes a component of cohesin, a multisubunit protein complex that provides sister chromatid cohesion along the length of a chromosome from DNA replication through prophase and prometaphase, after which it is dissociated in preparation for segregation during anaphase. [provided by RefSeq, Jul 2008]","start":136336233,"end":136752403,"strand":-1,"description":"stromal antigen 1 [Source:HGNC Symbol;Acc:HGNC:11354]"}, {"versioned_ensembl_gene_id":"ENSG00000260643.2","gene_symbol":"AC092718.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":81053587,"end":81096296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267423.1","gene_symbol":"AC005616.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28509238,"end":28518728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254194.5","gene_symbol":"AF279873.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33973701,"end":34009595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235931.2","gene_symbol":"LINC01553","gene_name":"long intergenic non-protein coding RNA 1553 [Source:HGNC Symbol;Acc:HGNC:23524]","synonyms":"AC023904.2,C10orf40","biotype":"lincRNA","ncbi_id":"283025","summary":null,"start":59955430,"end":59960913,"strand":-1,"description":"long intergenic non-protein coding RNA 1553 [Source:HGNC Symbol;Acc:HGNC:23524]"}, {"versioned_ensembl_gene_id":"ENSG00000241253.8","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31936032,"end":31942466,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000266976.1","gene_symbol":"AC079466.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28606688,"end":28615229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267537.1","gene_symbol":"AC079466.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28602379,"end":28648303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253642.5","gene_symbol":"AF279873.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33604856,"end":34039008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267243.6","gene_symbol":"AC005381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28437060,"end":28535277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234835.1","gene_symbol":"PHBP13","gene_name":"prohibitin pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39292]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418843","summary":null,"start":35251070,"end":35251829,"strand":1,"description":"prohibitin pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39292]"}, {"versioned_ensembl_gene_id":"ENSG00000165055.15","gene_symbol":"METTL2B","gene_name":"methyltransferase like 2B [Source:HGNC Symbol;Acc:HGNC:18272]","synonyms":"METTL2,METL,FLJ11350","biotype":"protein_coding","ncbi_id":"55798","summary":"This gene is a member of a family of methyltransferases that share homology with, but are distinct from, the UbiE family of methyltransferases. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":128476729,"end":128506602,"strand":1,"description":"methyltransferase like 2B [Source:HGNC Symbol;Acc:HGNC:18272]"}, {"versioned_ensembl_gene_id":"ENSG00000278985.1","gene_symbol":"AC092718.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80982319,"end":80984094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255427.1","gene_symbol":"AC087783.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34570876,"end":34573982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103121.8","gene_symbol":"CMC2","gene_name":"C-X9-C motif containing 2 [Source:HGNC Symbol;Acc:HGNC:24447]","synonyms":"MGC45036,DC13,C16orf61","biotype":"protein_coding","ncbi_id":"56942","summary":null,"start":80966448,"end":81020270,"strand":-1,"description":"C-X9-C motif containing 2 [Source:HGNC Symbol;Acc:HGNC:24447]"}, {"versioned_ensembl_gene_id":"ENSG00000253569.1","gene_symbol":"VENTXP5","gene_name":"VENT homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32214]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442384","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":33722305,"end":33723079,"strand":-1,"description":"VENT homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32214]"}, {"versioned_ensembl_gene_id":"ENSG00000180660.7","gene_symbol":"MAB21L1","gene_name":"mab-21 like 1 [Source:HGNC Symbol;Acc:HGNC:6757]","synonyms":"CAGR1","biotype":"protein_coding","ncbi_id":"4081","summary":"This gene is similar to the MAB-21 cell fate-determining gene found in C. elegans. It may be involved in eye and cerebellum development, and it has been proposed that expansion of a trinucleotide repeat region in the 5' UTR may play a role in a variety of psychiatric disorders. [provided by RefSeq, Oct 2008]","start":35474182,"end":35477209,"strand":-1,"description":"mab-21 like 1 [Source:HGNC Symbol;Acc:HGNC:6757]"}, {"versioned_ensembl_gene_id":"ENSG00000240738.1","gene_symbol":"AF279873.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33859480,"end":33860223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188512.6","gene_symbol":"AF279873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33969567,"end":33969879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253684.1","gene_symbol":"BUD31P1","gene_name":"BUD31 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480331","summary":null,"start":33641581,"end":33641939,"strand":-1,"description":"BUD31 homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51561]"}, {"versioned_ensembl_gene_id":"ENSG00000121864.9","gene_symbol":"ZNF639","gene_name":"zinc finger protein 639 [Source:HGNC Symbol;Acc:HGNC:30950]","synonyms":"ZASC1,ANC-2H01","biotype":"protein_coding","ncbi_id":"51193","summary":"This gene encodes a member of the Kruppel-like zinc finger family of proteins. Amplification and overexpression of this gene have been observed in esophageal squamous cell carcinoma. The encoded protein has been shown to bind DNA in a sequence-specific manner and may regulate HIV-1 gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":179322991,"end":179338583,"strand":1,"description":"zinc finger protein 639 [Source:HGNC Symbol;Acc:HGNC:30950]"}, {"versioned_ensembl_gene_id":"ENSG00000272002.1","gene_symbol":"AC010904.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7260871,"end":7261504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281999.1","gene_symbol":"AC083849.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148444254,"end":148444767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282044.1","gene_symbol":"AC083849.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148439467,"end":148475983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218676.1","gene_symbol":"BRD7P4","gene_name":"bromodomain containing 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37630]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287229","summary":null,"start":111430260,"end":111431781,"strand":1,"description":"bromodomain containing 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37630]"}, {"versioned_ensembl_gene_id":"ENSG00000120053.10","gene_symbol":"GOT1","gene_name":"glutamic-oxaloacetic transaminase 1 [Source:HGNC Symbol;Acc:HGNC:4432]","synonyms":"AST1","biotype":"protein_coding","ncbi_id":"2805","summary":"Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. [provided by RefSeq, Jul 2008]","start":99396870,"end":99430624,"strand":-1,"description":"glutamic-oxaloacetic transaminase 1 [Source:HGNC Symbol;Acc:HGNC:4432]"}, {"versioned_ensembl_gene_id":"ENSG00000254664.1","gene_symbol":"AC103681.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45215815,"end":45235292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000019485.13","gene_symbol":"PRDM11","gene_name":"PR/SET domain 11 [Source:HGNC Symbol;Acc:HGNC:13996]","synonyms":"PFM8","biotype":"protein_coding","ncbi_id":"56981","summary":null,"start":45095806,"end":45235110,"strand":1,"description":"PR/SET domain 11 [Source:HGNC Symbol;Acc:HGNC:13996]"}, {"versioned_ensembl_gene_id":"ENSG00000159337.6","gene_symbol":"PLA2G4D","gene_name":"phospholipase A2 group IVD [Source:HGNC Symbol;Acc:HGNC:30038]","synonyms":"cPLA2delta","biotype":"protein_coding","ncbi_id":"283748","summary":"The phospholipase A2 enzyme family, including PLA2G4D, catalyze the hydrolysis of glycerophospholipids at the sn-2 position and then liberate free fatty acids and lysophospholipids (Chiba et al., 2004 [PubMed 14709560]).[supplied by OMIM, Jun 2009]","start":42067009,"end":42094554,"strand":-1,"description":"phospholipase A2 group IVD [Source:HGNC Symbol;Acc:HGNC:30038]"}, {"versioned_ensembl_gene_id":"ENSG00000108055.9","gene_symbol":"SMC3","gene_name":"structural maintenance of chromosomes 3 [Source:HGNC Symbol;Acc:HGNC:2468]","synonyms":"HCAP,CSPG6,bamacan,BAM,SMC3L1","biotype":"protein_coding","ncbi_id":"9126","summary":"This gene belongs to the SMC3 subfamily of SMC proteins. The encoded protein occurs in certain cell types as either an intracellular, nuclear protein or a secreted protein. The nuclear form, known as structural maintenance of chromosomes 3, is a component of the multimeric cohesin complex that holds together sister chromatids during mitosis, enabling proper chromosome segregation. Post-translational modification of the encoded protein by the addition of chondroitin sulfate chains gives rise to the secreted proteoglycan bamacan, an abundant basement membrane protein. [provided by RefSeq, Jul 2008]","start":110567691,"end":110604636,"strand":1,"description":"structural maintenance of chromosomes 3 [Source:HGNC Symbol;Acc:HGNC:2468]"}, {"versioned_ensembl_gene_id":"ENSG00000103222.18","gene_symbol":"ABCC1","gene_name":"ATP binding cassette subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:51]","synonyms":"MRP1,MRP,GS-X","biotype":"protein_coding","ncbi_id":"4363","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra-and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This full transporter is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a multispecific organic anion transporter, with oxidized glutatione, cysteinyl leukotrienes, and activated aflatoxin B1 as substrates. This protein also transports glucuronides and sulfate conjugates of steroid hormones and bile salts. Alternatively spliced variants of this gene have been described but their full-length nature is unknown. [provided by RefSeq, Apr 2012]","start":15949577,"end":16143074,"strand":1,"description":"ATP binding cassette subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:51]"}, {"versioned_ensembl_gene_id":"ENSG00000236003.1","gene_symbol":"AC007731.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20522070,"end":20523870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000055732.12","gene_symbol":"MCOLN3","gene_name":"mucolipin 3 [Source:HGNC Symbol;Acc:HGNC:13358]","synonyms":"TRPML3,TRP-ML3,FLJ11006","biotype":"protein_coding","ncbi_id":"55283","summary":"This gene encodes one of members of the mucolipin cation channel proteins. Mutation studies of the highly similar protein in mice have shown that the protein is found in cochlea hair cells, and mutant mice show early-onset hearing loss and balance problems. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":85018082,"end":85048499,"strand":-1,"description":"mucolipin 3 [Source:HGNC Symbol;Acc:HGNC:13358]"}, {"versioned_ensembl_gene_id":"ENSG00000198580.7","gene_symbol":"AC073343.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6673494,"end":6676366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259415.1","gene_symbol":"AC012291.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":84753122,"end":84754502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238134.8","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"C6orf30,G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31956231,"end":31974166,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000228010.5","gene_symbol":"AC073343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6663974,"end":6708901,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000074410.13","gene_symbol":"CA12","gene_name":"carbonic anhydrase 12 [Source:HGNC Symbol;Acc:HGNC:1371]","synonyms":"HsT18816","biotype":"protein_coding","ncbi_id":"771","summary":"Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. This gene product is a type I membrane protein that is highly expressed in normal tissues, such as kidney, colon and pancreas, and has been found to be overexpressed in 10% of clear cell renal carcinomas. Three transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2014]","start":63321378,"end":63382161,"strand":-1,"description":"carbonic anhydrase 12 [Source:HGNC Symbol;Acc:HGNC:1371]"}, {"versioned_ensembl_gene_id":"ENSG00000185739.13","gene_symbol":"SRL","gene_name":"sarcalumenin [Source:HGNC Symbol;Acc:HGNC:11295]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6345","summary":null,"start":4189374,"end":4242080,"strand":-1,"description":"sarcalumenin [Source:HGNC Symbol;Acc:HGNC:11295]"}, {"versioned_ensembl_gene_id":"ENSG00000099917.17","gene_symbol":"MED15","gene_name":"mediator complex subunit 15 [Source:HGNC Symbol;Acc:HGNC:14248]","synonyms":"TNRC7,TIG-1,PCQAP,CAG7A,Arc105","biotype":"protein_coding","ncbi_id":"51586","summary":"The protein encoded by this gene is a subunit of the multiprotein complexes PC2 and ARC/DRIP and may function as a transcriptional coactivator in RNA polymerase II transcription. This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":20495913,"end":20587632,"strand":1,"description":"mediator complex subunit 15 [Source:HGNC Symbol;Acc:HGNC:14248]"}, {"versioned_ensembl_gene_id":"ENSG00000235004.1","gene_symbol":"USP9YP30","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:38766]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874384","summary":null,"start":25723016,"end":25724186,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:38766]"}, {"versioned_ensembl_gene_id":"ENSG00000232614.1","gene_symbol":"USP9YP9","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38435]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421220","summary":null,"start":25730011,"end":25735160,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38435]"}, {"versioned_ensembl_gene_id":"ENSG00000070950.9","gene_symbol":"RAD18","gene_name":"RAD18, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:18278]","synonyms":"RNF73","biotype":"protein_coding","ncbi_id":"56852","summary":"The protein encoded by this gene is highly similar to S. cerevisiae DNA damage repair protein Rad18. Yeast Rad18 functions through its interaction with Rad6, which is an ubiquitin-conjugating enzyme required for post-replication repair of damaged DNA. Similar to its yeast counterpart, this protein is able to interact with the human homolog of yeast Rad6 protein through a conserved ring-finger motif. Mutation of this motif results in defective replication of UV-damaged DNA and hypersensitivity to multiple mutagens. [provided by RefSeq, Jul 2008]","start":8775402,"end":8963773,"strand":-1,"description":"RAD18, E3 ubiquitin protein ligase [Source:HGNC Symbol;Acc:HGNC:18278]"}, {"versioned_ensembl_gene_id":"ENSG00000110931.18","gene_symbol":"CAMKK2","gene_name":"calcium/calmodulin dependent protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:1470]","synonyms":"MGC15254,KIAA0787,CAMKKB,CAMKK","biotype":"protein_coding","ncbi_id":"10645","summary":"The product of this gene belongs to the Serine/Threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. The major isoform of this gene plays a role in the calcium/calmodulin-dependent (CaM) kinase cascade by phosphorylating the downstream kinases CaMK1 and CaMK4. Protein products of this gene also phosphorylate AMP-activated protein kinase (AMPK). This gene has its strongest expression in the brain and influences signalling cascades involved with learning and memory, neuronal differentiation and migration, neurite outgrowth, and synapse formation. Alternative splicing results in multiple transcript variants encoding distinct isoforms. The identified isoforms differ in their ability to undergo autophosphorylation and to phosphorylate downstream kinases. [provided by RefSeq, Jul 2012]","start":121237691,"end":121298308,"strand":-1,"description":"calcium/calmodulin dependent protein kinase kinase 2 [Source:HGNC Symbol;Acc:HGNC:1470]"}, {"versioned_ensembl_gene_id":"ENSG00000231141.1","gene_symbol":"TTTY3","gene_name":"testis-specific transcript, Y-linked 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16480]","synonyms":"TTY3,TTTY3A,LINC00121","biotype":"lincRNA","ncbi_id":"114760","summary":"There are two copies of this gene within the P1 palindrome on chromosome Y. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":25728490,"end":25733388,"strand":1,"description":"testis-specific transcript, Y-linked 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16480]"}, {"versioned_ensembl_gene_id":"ENSG00000231713.2","gene_symbol":"AF064860.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39727755,"end":39730680,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133026.12","gene_symbol":"MYH10","gene_name":"myosin heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:7568]","synonyms":"NMMHCB","biotype":"protein_coding","ncbi_id":"4628","summary":"This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-10 (MYO10). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene have been associated with May-Hegglin anomaly and developmental defects in brain and heart. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":8474205,"end":8630761,"strand":-1,"description":"myosin heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:7568]"}, {"versioned_ensembl_gene_id":"ENSG00000183067.5","gene_symbol":"IGSF5","gene_name":"immunoglobulin superfamily member 5 [Source:HGNC Symbol;Acc:HGNC:5952]","synonyms":"JAM4","biotype":"protein_coding","ncbi_id":"150084","summary":null,"start":39745407,"end":39802096,"strand":1,"description":"immunoglobulin superfamily member 5 [Source:HGNC Symbol;Acc:HGNC:5952]"}, {"versioned_ensembl_gene_id":"ENSG00000177119.15","gene_symbol":"ANO6","gene_name":"anoctamin 6 [Source:HGNC Symbol;Acc:HGNC:25240]","synonyms":"TMEM16F,DKFZp313M0720","biotype":"protein_coding","ncbi_id":"196527","summary":"This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]","start":45215987,"end":45440404,"strand":1,"description":"anoctamin 6 [Source:HGNC Symbol;Acc:HGNC:25240]"}, {"versioned_ensembl_gene_id":"ENSG00000250081.1","gene_symbol":"AC025176.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65486444,"end":65487048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267799.1","gene_symbol":"MAN1A2P1","gene_name":"mannosidase alpha class 1A member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50488]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129507","summary":null,"start":28790812,"end":28792871,"strand":-1,"description":"mannosidase alpha class 1A member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50488]"}, {"versioned_ensembl_gene_id":"ENSG00000224934.3","gene_symbol":"AL391684.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99431191,"end":99461743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091704.9","gene_symbol":"CPA1","gene_name":"carboxypeptidase A1 [Source:HGNC Symbol;Acc:HGNC:2296]","synonyms":"CPA","biotype":"protein_coding","ncbi_id":"1357","summary":"This gene encodes a member of the carboxypeptidase A family of zinc metalloproteases. This enzyme is produced in the pancreas and preferentially cleaves C-terminal branched-chain and aromatic amino acids from dietary proteins. This gene and several family members are present in a gene cluster on chromosome 7. Mutations in this gene may be linked to chronic pancreatitis, while elevated protein levels may be associated with pancreatic cancer. [provided by RefSeq, Jan 2015]","start":130380339,"end":130388114,"strand":1,"description":"carboxypeptidase A1 [Source:HGNC Symbol;Acc:HGNC:2296]"}, {"versioned_ensembl_gene_id":"ENSG00000078369.17","gene_symbol":"GNB1","gene_name":"G protein subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:4396]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2782","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":1785285,"end":1891117,"strand":-1,"description":"G protein subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:4396]"}, {"versioned_ensembl_gene_id":"ENSG00000267617.1","gene_symbol":"AC007795.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28869796,"end":28879170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280278.1","gene_symbol":"FLJ30679","gene_name":"uncharacterized protein FLJ30679 [Source:NCBI gene;Acc:146512]","synonyms":null,"biotype":"TEC","ncbi_id":"146512","summary":null,"start":86555320,"end":86557299,"strand":1,"description":"uncharacterized protein FLJ30679 [Source:NCBI gene;Acc:146512]"}, {"versioned_ensembl_gene_id":"ENSG00000267528.1","gene_symbol":"AC008991.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28883430,"end":28953245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267027.1","gene_symbol":"AC011524.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28949437,"end":28950200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267683.1","gene_symbol":"AC008991.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28892931,"end":28895949,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078018.19","gene_symbol":"MAP2","gene_name":"microtubule associated protein 2 [Source:HGNC Symbol;Acc:HGNC:6839]","synonyms":"MAP2C,MAP2B,MAP2A","biotype":"protein_coding","ncbi_id":"4133","summary":"This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The products of similar genes in rat and mouse are neuron-specific cytoskeletal proteins that are enriched in dentrites, implicating a role in determining and stabilizing dentritic shape during neuron development. A number of alternatively spliced variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2010]","start":209424058,"end":209734118,"strand":1,"description":"microtubule associated protein 2 [Source:HGNC Symbol;Acc:HGNC:6839]"}, {"versioned_ensembl_gene_id":"ENSG00000120899.17","gene_symbol":"PTK2B","gene_name":"protein tyrosine kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:9612]","synonyms":"RAFTK,PYK2,PTK,FAK2,CAKB,CADTK","biotype":"protein_coding","ncbi_id":"2185","summary":"This gene encodes a cytoplasmic protein tyrosine kinase which is involved in calcium-induced regulation of ion channels and activation of the map kinase signaling pathway. The encoded protein may represent an important signaling intermediate between neuropeptide-activated receptors or neurotransmitters that increase calcium flux and the downstream signals that regulate neuronal activity. The encoded protein undergoes rapid tyrosine phosphorylation and activation in response to increases in the intracellular calcium concentration, nicotinic acetylcholine receptor activation, membrane depolarization, or protein kinase C activation. This protein has been shown to bind CRK-associated substrate, nephrocystin, GTPase regulator associated with FAK, and the SH2 domain of GRB2. The encoded protein is a member of the FAK subfamily of protein tyrosine kinases but lacks significant sequence similarity to kinases from other subfamilies. Four transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":27311482,"end":27459391,"strand":1,"description":"protein tyrosine kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:9612]"}, {"versioned_ensembl_gene_id":"ENSG00000176692.5","gene_symbol":"FOXC2","gene_name":"forkhead box C2 [Source:HGNC Symbol;Acc:HGNC:3801]","synonyms":"MFH-1,FKHL14","biotype":"protein_coding","ncbi_id":"2303","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the development of mesenchymal tissues. [provided by RefSeq, Jul 2008]","start":86567251,"end":86569728,"strand":1,"description":"forkhead box C2 [Source:HGNC Symbol;Acc:HGNC:3801]"}, {"versioned_ensembl_gene_id":"ENSG00000220506.2","gene_symbol":"AL136310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111494991,"end":111495713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260944.1","gene_symbol":"FOXC2-AS1","gene_name":"FOXC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50665]","synonyms":"ODRUL","biotype":"antisense_RNA","ncbi_id":"103752587","summary":null,"start":86565145,"end":86567761,"strand":-1,"description":"FOXC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50665]"}, {"versioned_ensembl_gene_id":"ENSG00000225991.1","gene_symbol":"RPL23AP34","gene_name":"ribosomal protein L23a pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271294","summary":null,"start":28308161,"end":28308570,"strand":1,"description":"ribosomal protein L23a pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36035]"}, {"versioned_ensembl_gene_id":"ENSG00000270846.1","gene_symbol":"AC021171.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27896116,"end":27897195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228778.2","gene_symbol":"AL513542.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99526948,"end":99528467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243147.7","gene_symbol":"MRPL33","gene_name":"mitochondrial ribosomal protein L33 [Source:HGNC Symbol;Acc:HGNC:14487]","synonyms":"RPL33L,C2orf1","biotype":"protein_coding","ncbi_id":"9553","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":27771717,"end":27988087,"strand":1,"description":"mitochondrial ribosomal protein L33 [Source:HGNC Symbol;Acc:HGNC:14487]"}, {"versioned_ensembl_gene_id":"ENSG00000257582.5","gene_symbol":"LINC01475","gene_name":"long intergenic non-protein coding RNA 1475 [Source:HGNC Symbol;Acc:HGNC:51113]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927324","summary":null,"start":99526350,"end":99531177,"strand":-1,"description":"long intergenic non-protein coding RNA 1475 [Source:HGNC Symbol;Acc:HGNC:51113]"}, {"versioned_ensembl_gene_id":"ENSG00000267240.1","gene_symbol":"AC011524.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28960506,"end":28964943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100105.17","gene_symbol":"PATZ1","gene_name":"POZ/BTB and AT hook containing zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13071]","synonyms":"MAZR,dJ400N23,ZSG,ZNF278,ZBTB19,RIAZ,PATZ","biotype":"protein_coding","ncbi_id":"23598","summary":"The protein encoded by this gene contains an A-T hook DNA binding motif which usually binds to other DNA binding structures to play an important role in chromatin modeling and transcription regulation. Its Poz domain is thought to function as a site for protein-protein interaction and is required for transcriptional repression, and the zinc-fingers comprise the DNA binding domain. Since the encoded protein has typical features of a transcription factor, it is postulated to be a repressor of gene expression. In small round cell sarcoma, this gene is fused to EWS by a small inversion of 22q, then the hybrid is thought to be translocated (t(1;22)(p36.1;q12). The rearrangement of chromosome 22 involves intron 8 of EWS and exon 1 of this gene creating a chimeric sequence containing the transactivation domain of EWS fused to zinc finger domain of this protein. This is a distinct example of an intra-chromosomal rearrangement of chromosome 22. Four alternatively spliced transcript variants are described for this gene. [provided by RefSeq, Jul 2008]","start":31325804,"end":31346232,"strand":-1,"description":"POZ/BTB and AT hook containing zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:13071]"}, {"versioned_ensembl_gene_id":"ENSG00000176678.5","gene_symbol":"FOXL1","gene_name":"forkhead box L1 [Source:HGNC Symbol;Acc:HGNC:3817]","synonyms":"FREAC7,FKHL11,FKH6","biotype":"protein_coding","ncbi_id":"2300","summary":"This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors are characterized by a distinct DNA-binding forkhead domain and play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. [provided by RefSeq, Nov 2012]","start":86576368,"end":86582160,"strand":1,"description":"forkhead box L1 [Source:HGNC Symbol;Acc:HGNC:3817]"}, {"versioned_ensembl_gene_id":"ENSG00000116183.10","gene_symbol":"PAPPA2","gene_name":"pappalysin 2 [Source:HGNC Symbol;Acc:HGNC:14615]","synonyms":"PLAC3,PAPPE,PAPP-A2","biotype":"protein_coding","ncbi_id":"60676","summary":"This gene encodes a member of the pappalysin family of metzincin metalloproteinases. The encoded protein cleaves insulin-like growth factor-binding protein 5 and is thought to be a local regulator of insulin-like growth factor (IGF) bioavailability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":176463171,"end":176845605,"strand":1,"description":"pappalysin 2 [Source:HGNC Symbol;Acc:HGNC:14615]"}, {"versioned_ensembl_gene_id":"ENSG00000119919.10","gene_symbol":"NKX2-3","gene_name":"NK2 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:7836]","synonyms":"NKX2C,NKX2.3,CSX3,NKX4-3","biotype":"protein_coding","ncbi_id":"159296","summary":"This gene encodes a homeodomain-containing transcription factor. The encoded protein is a member of the NKX family of homeodomain transcription factors. Studies of similar proteins in mouse and rat have indicated a potential role in cellular differentiation.[provided by RefSeq, Mar 2010]","start":99532933,"end":99536524,"strand":1,"description":"NK2 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:7836]"}, {"versioned_ensembl_gene_id":"ENSG00000267339.5","gene_symbol":"LINC00906","gene_name":"long intergenic non-protein coding RNA 906 [Source:HGNC Symbol;Acc:HGNC:27121]","synonyms":null,"biotype":"lincRNA","ncbi_id":"148145","summary":null,"start":28965131,"end":28970874,"strand":1,"description":"long intergenic non-protein coding RNA 906 [Source:HGNC Symbol;Acc:HGNC:27121]"}, {"versioned_ensembl_gene_id":"ENSG00000257022.1","gene_symbol":"AC008250.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21827210,"end":21887957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275567.1","gene_symbol":"AC008250.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21828360,"end":21828564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137225.12","gene_symbol":"CAPN11","gene_name":"calpain 11 [Source:HGNC Symbol;Acc:HGNC:1478]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11131","summary":"Calpains constitute a family of intracellular calcium-dependent cysteine proteases. There are eight members in this superfamily. They consist of a variable 80 kDa subunit and an invariant 30 kDa subunit. This calpain protein appears to have protease activity and calcium-binding ability. A similar mouse protein may play a functional role in spermatogenesis and in the regulation of calcium-dependent signal transduction events during meiosis. [provided by RefSeq, Dec 2008]","start":44158811,"end":44184402,"strand":1,"description":"calpain 11 [Source:HGNC Symbol;Acc:HGNC:1478]"}, {"versioned_ensembl_gene_id":"ENSG00000069431.11","gene_symbol":"ABCC9","gene_name":"ATP binding cassette subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:60]","synonyms":"SUR2,CMD1O","biotype":"protein_coding","ncbi_id":"10060","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is thought to form ATP-sensitive potassium channels in cardiac, skeletal, and vascular and non-vascular smooth muscle. Protein structure suggests a role as the drug-binding channel-modulating subunit of the extra-pancreatic ATP-sensitive potassium channels. Mutations in this gene are associated with cardiomyopathy dilated type 1O. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]","start":21797401,"end":21942529,"strand":-1,"description":"ATP binding cassette subfamily C member 9 [Source:HGNC Symbol;Acc:HGNC:60]"}, {"versioned_ensembl_gene_id":"ENSG00000250877.1","gene_symbol":"AC095056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72323028,"end":72330751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279142.1","gene_symbol":"AC009108.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":86595189,"end":86597639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156140.9","gene_symbol":"ADAMTS3","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 3 [Source:HGNC Symbol;Acc:HGNC:219]","synonyms":"KIAA0366,ADAMTS-4","biotype":"protein_coding","ncbi_id":"9508","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protease. This protease, a member of the procollagen aminopropeptidase subfamily of proteins, may play a role in the processing of type II fibrillar collagen in articular cartilage. [provided by RefSeq, Feb 2016]","start":72280969,"end":72569386,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 3 [Source:HGNC Symbol;Acc:HGNC:219]"}, {"versioned_ensembl_gene_id":"ENSG00000223522.1","gene_symbol":"AC093690.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28307691,"end":28310459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260387.1","gene_symbol":"AC009108.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86636328,"end":86637145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261161.1","gene_symbol":"AC009154.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86646301,"end":86668923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270528.1","gene_symbol":"AC021171.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28015777,"end":28016482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171174.13","gene_symbol":"RBKS","gene_name":"ribokinase [Source:HGNC Symbol;Acc:HGNC:30325]","synonyms":"RBSK,DKFZp686G13268","biotype":"protein_coding","ncbi_id":"64080","summary":"This gene encodes a member of the carbohydrate kinase PfkB family. The encoded protein phosphorylates ribose to form ribose-5-phosphate in the presence of ATP and magnesium as a first step in ribose metabolism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":27781364,"end":27891098,"strand":-1,"description":"ribokinase [Source:HGNC Symbol;Acc:HGNC:30325]"}, {"versioned_ensembl_gene_id":"ENSG00000274478.1","gene_symbol":"AC009154.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86698118,"end":86698841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229360.1","gene_symbol":"PPP1R2P5","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:16320]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649489","summary":null,"start":106940880,"end":106941482,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:16320]"}, {"versioned_ensembl_gene_id":"ENSG00000162643.12","gene_symbol":"WDR63","gene_name":"WD repeat domain 63 [Source:HGNC Symbol;Acc:HGNC:30711]","synonyms":"NYD-SP29,FLJ30067,DIC3","biotype":"protein_coding","ncbi_id":"126820","summary":null,"start":84999147,"end":85133138,"strand":1,"description":"WD repeat domain 63 [Source:HGNC Symbol;Acc:HGNC:30711]"}, {"versioned_ensembl_gene_id":"ENSG00000226905.1","gene_symbol":"AC005040.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106963193,"end":106963674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116785.13","gene_symbol":"CFHR3","gene_name":"complement factor H related 3 [Source:HGNC Symbol;Acc:HGNC:16980]","synonyms":"DOWN16,CFHL3,HLF4,FHR3,FHR-3","biotype":"protein_coding","ncbi_id":"10878","summary":"The protein encoded by this gene is a secreted protein, which belongs to the complement factor H-related protein family. It binds to heparin, and may be involved in complement regulation. Mutations in this gene are associated with decreased risk of age-related macular degeneration, and with an increased risk of atypical hemolytic-uremic syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":196774795,"end":196795406,"strand":1,"description":"complement factor H related 3 [Source:HGNC Symbol;Acc:HGNC:16980]"}, {"versioned_ensembl_gene_id":"ENSG00000260213.5","gene_symbol":"AC092718.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81016792,"end":81035759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245059.2","gene_symbol":"AC092718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81077319,"end":81078861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099995.18","gene_symbol":"SF3A1","gene_name":"splicing factor 3a subunit 1 [Source:HGNC Symbol;Acc:HGNC:10765]","synonyms":"SF3a120,SAP114,PRPF21,Prp21","biotype":"protein_coding","ncbi_id":"10291","summary":"This gene encodes a subunit of the splicing factor 3a protein complex. The splicing factor 3a heterotrimer is a component of the mature U2 small nuclear ribonucleoprotein particle (snRNP). U2 small nuclear ribonucleoproteins play a critical role in spliceosome assembly and pre-mRNA splicing. [provided by RefSeq, Aug 2014]","start":30331988,"end":30356947,"strand":-1,"description":"splicing factor 3a subunit 1 [Source:HGNC Symbol;Acc:HGNC:10765]"}, {"versioned_ensembl_gene_id":"ENSG00000244462.7","gene_symbol":"RBM12","gene_name":"RNA binding motif protein 12 [Source:HGNC Symbol;Acc:HGNC:9898]","synonyms":"SWAN,KIAA0765,HRIHFB2091","biotype":"protein_coding","ncbi_id":"10137","summary":"This gene encodes a protein that contains several RNA-binding motifs, potential transmembrane domains, and proline-rich regions. This gene and the gene for copine I overlap at map location 20q11.21. Alternative splicing in the 5' UTR results in four transcript variants. All variants encode the same protein. [provided by RefSeq, Nov 2010]","start":35648925,"end":35664956,"strand":-1,"description":"RNA binding motif protein 12 [Source:HGNC Symbol;Acc:HGNC:9898]"}, {"versioned_ensembl_gene_id":"ENSG00000166455.13","gene_symbol":"C16orf46","gene_name":"chromosome 16 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:26525]","synonyms":"FLJ32702","biotype":"protein_coding","ncbi_id":"123775","summary":null,"start":81053497,"end":81077267,"strand":-1,"description":"chromosome 16 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:26525]"}, {"versioned_ensembl_gene_id":"ENSG00000241353.3","gene_symbol":"PPP1R2P4","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16319]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728970","summary":null,"start":46437394,"end":46437988,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:16319]"}, {"versioned_ensembl_gene_id":"ENSG00000228839.5","gene_symbol":"PIK3IP1-AS1","gene_name":"PIK3IP1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:41072]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929760","summary":null,"start":31292499,"end":31338021,"strand":1,"description":"PIK3IP1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:41072]"}, {"versioned_ensembl_gene_id":"ENSG00000225588.2","gene_symbol":"AC096669.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107362282,"end":107407329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100100.12","gene_symbol":"PIK3IP1","gene_name":"phosphoinositide-3-kinase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24942]","synonyms":"MGC17330,HGFL","biotype":"protein_coding","ncbi_id":"113791","summary":null,"start":31281593,"end":31292534,"strand":-1,"description":"phosphoinositide-3-kinase interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:24942]"}, {"versioned_ensembl_gene_id":"ENSG00000137825.10","gene_symbol":"ITPKA","gene_name":"inositol-trisphosphate 3-kinase A [Source:HGNC Symbol;Acc:HGNC:6178]","synonyms":"IP3KA,IP3-3KA","biotype":"protein_coding","ncbi_id":"3706","summary":"Regulates inositol phosphate metabolism by phosphorylation of second messenger inositol 1,4,5-trisphosphate to Ins(1,3,4,5)P4. The activity of the inositol 1,4,5-trisphosphate 3-kinase is responsible for regulating the levels of a large number of inositol polyphosphates that are important in cellular signaling. Both calcium/calmodulin and protein phosphorylation mechanisms control its activity. It is also a substrate for the cyclic AMP-dependent protein kinase, calcium/calmodulin- dependent protein kinase II, and protein kinase C in vitro.[provided by RefSeq, Apr 2011]","start":41493393,"end":41503551,"strand":1,"description":"inositol-trisphosphate 3-kinase A [Source:HGNC Symbol;Acc:HGNC:6178]"}, {"versioned_ensembl_gene_id":"ENSG00000248188.2","gene_symbol":"AC005798.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15743196,"end":15743582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237514.3","gene_symbol":"PTP4A1P7","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:41934]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421681","summary":null,"start":176616273,"end":176616786,"strand":-1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:41934]"}, {"versioned_ensembl_gene_id":"ENSG00000233315.1","gene_symbol":"CR388372.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30506497,"end":30509451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224568.1","gene_symbol":"LINC01886","gene_name":"long intergenic non-protein coding RNA 1886 [Source:HGNC Symbol;Acc:HGNC:52705]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373537","summary":null,"start":107529487,"end":107556326,"strand":1,"description":"long intergenic non-protein coding RNA 1886 [Source:HGNC Symbol;Acc:HGNC:52705]"}, {"versioned_ensembl_gene_id":"ENSG00000235250.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31924830,"end":31932095,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000270490.1","gene_symbol":"AC110048.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66808404,"end":66810560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277152.1","gene_symbol":"AC110048.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66860303,"end":66867023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206372.11","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31888164,"end":31936056,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000101198.14","gene_symbol":"NKAIN4","gene_name":"sodium/potassium transporting ATPase interacting 4 [Source:HGNC Symbol;Acc:HGNC:16191]","synonyms":"FAM77A,C20orf58,bA261N11.2","biotype":"protein_coding","ncbi_id":"128414","summary":"NKAIN4 is a member of a family of mammalian proteins (see NKAIN1; MIM 612871) with similarity to Drosophila Nkain and interacts with the beta subunit of Na,K-ATPase (ATP1B1; MIM 182330) (Gorokhova et al., 2007 [PubMed 17606467]).[supplied by OMIM, Jun 2009]","start":63240784,"end":63272694,"strand":-1,"description":"sodium/potassium transporting ATPase interacting 4 [Source:HGNC Symbol;Acc:HGNC:16191]"}, {"versioned_ensembl_gene_id":"ENSG00000254079.1","gene_symbol":"AC012339.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95947781,"end":95948233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196811.11","gene_symbol":"CHRNG","gene_name":"cholinergic receptor nicotinic gamma subunit [Source:HGNC Symbol;Acc:HGNC:1967]","synonyms":"ACHRG","biotype":"protein_coding","ncbi_id":"1146","summary":"The mammalian muscle-type acetylcholine receptor is a transmembrane pentameric glycoprotein with two alpha subunits, one beta, one delta, and one epsilon (in adult skeletal muscle) or gamma (in fetal and denervated muscle) subunit. This gene, which encodes the gamma subunit, is expressed prior to the thirty-third week of gestation in humans. The gamma subunit of the acetylcholine receptor plays a role in neuromuscular organogenesis and ligand binding and disruption of gamma subunit expression prevents the correct localization of the receptor in cell membranes. Mutations in this gene cause Escobar syndrome and a lethal form of multiple pterygium syndrome. Muscle-type acetylcholine receptor is the major antigen in the autoimmune disease myasthenia gravis.[provided by RefSeq, Sep 2009]","start":232539727,"end":232546403,"strand":1,"description":"cholinergic receptor nicotinic gamma subunit [Source:HGNC Symbol;Acc:HGNC:1967]"}, {"versioned_ensembl_gene_id":"ENSG00000264971.1","gene_symbol":"PRR13P4","gene_name":"proline rich 13 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288008","summary":null,"start":49469803,"end":49470223,"strand":1,"description":"proline rich 13 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50617]"}, {"versioned_ensembl_gene_id":"ENSG00000237880.1","gene_symbol":"LINC01885","gene_name":"long intergenic non-protein coding RNA 1885 [Source:HGNC Symbol;Acc:HGNC:52704]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373538","summary":null,"start":107385632,"end":107542649,"strand":-1,"description":"long intergenic non-protein coding RNA 1885 [Source:HGNC Symbol;Acc:HGNC:52704]"}, {"versioned_ensembl_gene_id":"ENSG00000180914.10","gene_symbol":"OXTR","gene_name":"oxytocin receptor [Source:HGNC Symbol;Acc:HGNC:8529]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5021","summary":"The protein encoded by this gene belongs to the G-protein coupled receptor family and acts as a receptor for oxytocin. Its activity is mediated by G proteins which activate a phosphatidylinositol-calcium second messenger system. The oxytocin-oxytocin receptor system plays an important role in the uterus during parturition. [provided by RefSeq, Jul 2008]","start":8750408,"end":8769628,"strand":-1,"description":"oxytocin receptor [Source:HGNC Symbol;Acc:HGNC:8529]"}, {"versioned_ensembl_gene_id":"ENSG00000147251.15","gene_symbol":"DOCK11","gene_name":"dedicator of cytokinesis 11 [Source:HGNC Symbol;Acc:HGNC:23483]","synonyms":"ZIZ2,FLJ43653,FLJ32122,ACG","biotype":"protein_coding","ncbi_id":"139818","summary":null,"start":118495898,"end":118686163,"strand":1,"description":"dedicator of cytokinesis 11 [Source:HGNC Symbol;Acc:HGNC:23483]"}, {"versioned_ensembl_gene_id":"ENSG00000241067.2","gene_symbol":"AC136624.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16094192,"end":16095209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224040.1","gene_symbol":"HMGN1P4","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39336]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100036575","summary":null,"start":182942115,"end":182942404,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39336]"}, {"versioned_ensembl_gene_id":"ENSG00000259289.2","gene_symbol":"LINC02206","gene_name":"long intergenic non-protein coding RNA 2206 [Source:HGNC Symbol;Acc:HGNC:53072]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723481","summary":null,"start":66931537,"end":66956518,"strand":-1,"description":"long intergenic non-protein coding RNA 2206 [Source:HGNC Symbol;Acc:HGNC:53072]"}, {"versioned_ensembl_gene_id":"ENSG00000157060.15","gene_symbol":"SHCBP1L","gene_name":"SHC binding and spindle associated 1 like [Source:HGNC Symbol;Acc:HGNC:16788]","synonyms":"C1orf14","biotype":"protein_coding","ncbi_id":"81626","summary":"This gene encodes a Src homology 2 domain-binding protein 1-like protein. The encoded protein interacts with heat shock 70 kDa protein 2 and may be involved in maintaining spindle integrity during meiosis. This gene is located in region of chromoso0me 1 encompassing a prostate cancer susceptibility locus. [provided by RefSeq, Sep 2016]","start":182899865,"end":182953525,"strand":-1,"description":"SHC binding and spindle associated 1 like [Source:HGNC Symbol;Acc:HGNC:16788]"}, {"versioned_ensembl_gene_id":"ENSG00000235501.5","gene_symbol":"AC105942.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94927566,"end":94963270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272897.5","gene_symbol":"AL109827.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35632340,"end":35674544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259437.1","gene_symbol":"AC093334.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66919811,"end":66931755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229457.1","gene_symbol":"LINC01789","gene_name":"long intergenic non-protein coding RNA 1789 [Source:HGNC Symbol;Acc:HGNC:52578]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373536","summary":null,"start":107254691,"end":107365873,"strand":-1,"description":"long intergenic non-protein coding RNA 1789 [Source:HGNC Symbol;Acc:HGNC:52578]"}, {"versioned_ensembl_gene_id":"ENSG00000125995.15","gene_symbol":"ROMO1","gene_name":"reactive oxygen species modulator 1 [Source:HGNC Symbol;Acc:HGNC:16185]","synonyms":"MTGMP,C20orf52,bA353C18.2","biotype":"protein_coding","ncbi_id":"140823","summary":"The protein encoded by this gene is a mitochondrial membrane protein that is responsible for increasing the level of reactive oxygen species (ROS) in cells. The protein also has antimicrobial activity against a variety of bacteria by inducing bacterial membrane breakage. [provided by RefSeq, Nov 2014]","start":35699272,"end":35700984,"strand":1,"description":"reactive oxygen species modulator 1 [Source:HGNC Symbol;Acc:HGNC:16185]"}, {"versioned_ensembl_gene_id":"ENSG00000156304.14","gene_symbol":"SCAF4","gene_name":"SR-related CTD associated factor 4 [Source:HGNC Symbol;Acc:HGNC:19304]","synonyms":"SRA4,SFRS15,KIAA1172,DKFZp434E098","biotype":"protein_coding","ncbi_id":"57466","summary":"This gene likely encodes a member of the arginine/serine-rich splicing factor family. A similar protein in Rat appears to bind the large subunit of RNA polymerase II and provide a link between transcription and pre-mRNA splicing. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":31671033,"end":31732075,"strand":-1,"description":"SR-related CTD associated factor 4 [Source:HGNC Symbol;Acc:HGNC:19304]"}, {"versioned_ensembl_gene_id":"ENSG00000225326.1","gene_symbol":"USP9YP19","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38755]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100500797","summary":null,"start":25748596,"end":25750206,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38755]"}, {"versioned_ensembl_gene_id":"ENSG00000240758.2","gene_symbol":"AC010655.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":128455937,"end":128469197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223406.1","gene_symbol":"XKRYP5","gene_name":"XK related, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23912]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379032","summary":null,"start":25752388,"end":25752870,"strand":1,"description":"XK related, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23912]"}, {"versioned_ensembl_gene_id":"ENSG00000229343.1","gene_symbol":"CDY22P","gene_name":"chromodomain Y-linked 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:23866]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386744","summary":null,"start":25813013,"end":25814566,"strand":1,"description":"chromodomain Y-linked 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:23866]"}, {"versioned_ensembl_gene_id":"ENSG00000039123.15","gene_symbol":"SKIV2L2","gene_name":"Ski2 like RNA helicase 2 [Source:HGNC Symbol;Acc:HGNC:18734]","synonyms":"Mtr4,KIAA0052,fSAP118,Dob1","biotype":"protein_coding","ncbi_id":"23517","summary":null,"start":55307760,"end":55425581,"strand":1,"description":"Ski2 like RNA helicase 2 [Source:HGNC Symbol;Acc:HGNC:18734]"}, {"versioned_ensembl_gene_id":"ENSG00000166908.17","gene_symbol":"PIP4K2C","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 gamma [Source:HGNC Symbol;Acc:HGNC:23786]","synonyms":"PIP5K2C,FLJ22055","biotype":"protein_coding","ncbi_id":"79837","summary":null,"start":57591174,"end":57603418,"strand":1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 gamma [Source:HGNC Symbol;Acc:HGNC:23786]"}, {"versioned_ensembl_gene_id":"ENSG00000182533.6","gene_symbol":"CAV3","gene_name":"caveolin 3 [Source:HGNC Symbol;Acc:HGNC:1529]","synonyms":"VIP21,VIP-21,LQT9,LGMD1C","biotype":"protein_coding","ncbi_id":"859","summary":"This gene encodes a caveolin family member, which functions as a component of the caveolae plasma membranes found in most cell types. Caveolin proteins are proposed to be scaffolding proteins for organizing and concentrating certain caveolin-interacting molecules. Mutations identified in this gene lead to interference with protein oligomerization or intra-cellular routing, disrupting caveolae formation and resulting in Limb-Girdle muscular dystrophy type-1C (LGMD-1C), hyperCKemia or rippling muscle disease (RMD). Alternative splicing has been identified for this locus, with inclusion or exclusion of a differentially spliced intron. In addition, transcripts utilize multiple polyA sites and contain two potential translation initiation sites. [provided by RefSeq, Jul 2008]","start":8733800,"end":8841808,"strand":1,"description":"caveolin 3 [Source:HGNC Symbol;Acc:HGNC:1529]"}, {"versioned_ensembl_gene_id":"ENSG00000278351.1","gene_symbol":"AC009248.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45256473,"end":45256726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135245.9","gene_symbol":"HILPDA","gene_name":"hypoxia inducible lipid droplet associated [Source:HGNC Symbol;Acc:HGNC:28859]","synonyms":"HIG2,HIG-2,FLJ21076,C7orf68","biotype":"protein_coding","ncbi_id":"29923","summary":null,"start":128455849,"end":128458418,"strand":1,"description":"hypoxia inducible lipid droplet associated [Source:HGNC Symbol;Acc:HGNC:28859]"}, {"versioned_ensembl_gene_id":"ENSG00000257738.2","gene_symbol":"AC009248.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45200817,"end":45201551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134297.6","gene_symbol":"PLEKHA8P1","gene_name":"pleckstrin homology domain containing A8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30222]","synonyms":"PLEKHA9,FLJ14156","biotype":"transcribed_processed_pseudogene","ncbi_id":"51054","summary":null,"start":45173064,"end":45216041,"strand":-1,"description":"pleckstrin homology domain containing A8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30222]"}, {"versioned_ensembl_gene_id":"ENSG00000139832.4","gene_symbol":"RAB20","gene_name":"RAB20, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18260]","synonyms":"FLJ20429","biotype":"protein_coding","ncbi_id":"55647","summary":null,"start":110523066,"end":110561733,"strand":-1,"description":"RAB20, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18260]"}, {"versioned_ensembl_gene_id":"ENSG00000131238.17","gene_symbol":"PPT1","gene_name":"palmitoyl-protein thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:9325]","synonyms":"PPT,INCL,CLN1","biotype":"protein_coding","ncbi_id":"5538","summary":"The protein encoded by this gene is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. The encoded enzyme removes thioester-linked fatty acyl groups such as palmitate from cysteine residues. Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis 4 (CLN4). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2008]","start":40071461,"end":40097727,"strand":-1,"description":"palmitoyl-protein thioesterase 1 [Source:HGNC Symbol;Acc:HGNC:9325]"}, {"versioned_ensembl_gene_id":"ENSG00000215160.3","gene_symbol":"OR7E122P","gene_name":"olfactory receptor family 7 subfamily E member 122 pseudogene [Source:HGNC Symbol;Acc:HGNC:15050]","synonyms":"OST719","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81428","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":8682943,"end":8693701,"strand":1,"description":"olfactory receptor family 7 subfamily E member 122 pseudogene [Source:HGNC Symbol;Acc:HGNC:15050]"}, {"versioned_ensembl_gene_id":"ENSG00000273350.1","gene_symbol":"AC004832.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30420512,"end":30420912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125046.14","gene_symbol":"SSUH2","gene_name":"ssu-2 homolog (C. elegans) [Source:HGNC Symbol;Acc:HGNC:24809]","synonyms":"ssu-2,fls485,C3orf32","biotype":"protein_coding","ncbi_id":"51066","summary":null,"start":8619400,"end":8745040,"strand":-1,"description":"ssu-2 homolog (C. elegans) [Source:HGNC Symbol;Acc:HGNC:24809]"}, {"versioned_ensembl_gene_id":"ENSG00000099999.14","gene_symbol":"RNF215","gene_name":"ring finger protein 215 [Source:HGNC Symbol;Acc:HGNC:33434]","synonyms":null,"biotype":"protein_coding","ncbi_id":"200312","summary":null,"start":30368811,"end":30421771,"strand":-1,"description":"ring finger protein 215 [Source:HGNC Symbol;Acc:HGNC:33434]"}, {"versioned_ensembl_gene_id":"ENSG00000136205.16","gene_symbol":"TNS3","gene_name":"tensin 3 [Source:HGNC Symbol;Acc:HGNC:21616]","synonyms":"TENS1,TEM6,H_NH0549I23.2,FLJ13732","biotype":"protein_coding","ncbi_id":"64759","summary":null,"start":47275154,"end":47582558,"strand":-1,"description":"tensin 3 [Source:HGNC Symbol;Acc:HGNC:21616]"}, {"versioned_ensembl_gene_id":"ENSG00000275620.1","gene_symbol":"FLJ16779","gene_name":"uncharacterized LOC100192386 [Source:NCBI gene;Acc:100192386]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100192386","summary":null,"start":63253978,"end":63261615,"strand":1,"description":"uncharacterized LOC100192386 [Source:NCBI gene;Acc:100192386]"}, {"versioned_ensembl_gene_id":"ENSG00000260026.1","gene_symbol":"LINC02189","gene_name":"long intergenic non-protein coding RNA 2189 [Source:HGNC Symbol;Acc:HGNC:53051]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928614","summary":null,"start":86720688,"end":86721954,"strand":-1,"description":"long intergenic non-protein coding RNA 2189 [Source:HGNC Symbol;Acc:HGNC:53051]"}, {"versioned_ensembl_gene_id":"ENSG00000225766.9","gene_symbol":"DHRS4L1","gene_name":"dehydrogenase/reductase 4 like 1 [Source:HGNC Symbol;Acc:HGNC:19732]","synonyms":"SDR25C4","biotype":"processed_transcript","ncbi_id":"728635","summary":null,"start":24036453,"end":24051370,"strand":1,"description":"dehydrogenase/reductase 4 like 1 [Source:HGNC Symbol;Acc:HGNC:19732]"}, {"versioned_ensembl_gene_id":"ENSG00000267014.5","gene_symbol":"LINC01532","gene_name":"long intergenic non-protein coding RNA 1532 [Source:HGNC Symbol;Acc:HGNC:51272]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505835","summary":null,"start":29002555,"end":29013955,"strand":1,"description":"long intergenic non-protein coding RNA 1532 [Source:HGNC Symbol;Acc:HGNC:51272]"}, {"versioned_ensembl_gene_id":"ENSG00000134318.13","gene_symbol":"ROCK2","gene_name":"Rho associated coiled-coil containing protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:10252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9475","summary":"The protein encoded by this gene is a serine/threonine kinase that regulates cytokinesis, smooth muscle contraction, the formation of actin stress fibers and focal adhesions, and the activation of the c-fos serum response element. This protein, which is an isozyme of ROCK1 is a target for the small GTPase Rho. [provided by RefSeq, Jul 2008]","start":11179761,"end":11348330,"strand":-1,"description":"Rho associated coiled-coil containing protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:10252]"}, {"versioned_ensembl_gene_id":"ENSG00000262179.2","gene_symbol":"MYMX","gene_name":"myomixer, myoblast fusion factor [Source:HGNC Symbol;Acc:HGNC:52391]","synonyms":"MINION","biotype":"protein_coding","ncbi_id":"101929726","summary":null,"start":44216939,"end":44218236,"strand":1,"description":"myomixer, myoblast fusion factor [Source:HGNC Symbol;Acc:HGNC:52391]"}, {"versioned_ensembl_gene_id":"ENSG00000257674.1","gene_symbol":"AC020629.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42286911,"end":42288560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274943.1","gene_symbol":"AC079684.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42361267,"end":42361703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214078.12","gene_symbol":"CPNE1","gene_name":"copine 1 [Source:HGNC Symbol;Acc:HGNC:2314]","synonyms":"CPN1","biotype":"protein_coding","ncbi_id":"8904","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene encodes a calcium-dependent protein that also contains two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. However, the encoded protein does not contain a predicted signal sequence or transmembrane domains. This protein has a broad tissue distribution and it may function in membrane trafficking. This gene and the gene for RNA binding motif protein 12 overlap at map location 20q11.21. Alternate splicing results in multiple transcript variants encoding different proteins. [provided by RefSeq, Aug 2008]","start":35626031,"end":35664956,"strand":-1,"description":"copine 1 [Source:HGNC Symbol;Acc:HGNC:2314]"}, {"versioned_ensembl_gene_id":"ENSG00000177694.15","gene_symbol":"NAALADL2","gene_name":"N-acetylated alpha-linked acidic dipeptidase like 2 [Source:HGNC Symbol;Acc:HGNC:23219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"254827","summary":null,"start":174438573,"end":175810552,"strand":1,"description":"N-acetylated alpha-linked acidic dipeptidase like 2 [Source:HGNC Symbol;Acc:HGNC:23219]"}, {"versioned_ensembl_gene_id":"ENSG00000139174.11","gene_symbol":"PRICKLE1","gene_name":"prickle planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:17019]","synonyms":"RILP,FLJ31937,EPM1B","biotype":"protein_coding","ncbi_id":"144165","summary":"This gene encodes a nuclear receptor that may be a negative regulator of the Wnt/beta-catenin signaling pathway. The encoded protein localizes to the nuclear membrane and has been implicated in the nuclear trafficking of the transcription repressors REST/NRSF and REST4. Mutations in this gene have been linked to progressive myoclonus epilepsy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Sep 2009]","start":42456757,"end":42590355,"strand":-1,"description":"prickle planar cell polarity protein 1 [Source:HGNC Symbol;Acc:HGNC:17019]"}, {"versioned_ensembl_gene_id":"ENSG00000272601.1","gene_symbol":"AC010655.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":128466563,"end":128469171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230729.1","gene_symbol":"AL160270.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34521527,"end":34524241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168913.6","gene_symbol":"ENHO","gene_name":"energy homeostasis associated [Source:HGNC Symbol;Acc:HGNC:24838]","synonyms":"UNQ470,C9orf165","biotype":"protein_coding","ncbi_id":"375704","summary":null,"start":34521040,"end":34523041,"strand":-1,"description":"energy homeostasis associated [Source:HGNC Symbol;Acc:HGNC:24838]"}, {"versioned_ensembl_gene_id":"ENSG00000231460.2","gene_symbol":"AL365204.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23829670,"end":23849914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077264.14","gene_symbol":"PAK3","gene_name":"p21 (RAC1) activated kinase 3 [Source:HGNC Symbol;Acc:HGNC:8592]","synonyms":"MRX47,MRX30,hPAK3,bPAK","biotype":"protein_coding","ncbi_id":"5063","summary":"The protein encoded by this gene is a serine-threonine kinase and forms an activated complex with GTP-bound RAS-like (P21), CDC2 and RAC1. This protein may be necessary for dendritic development and for the rapid cytoskeletal reorganization in dendritic spines associated with synaptic plasticity. Defects in this gene are the cause of a non-syndromic form of X-linked intellectual disability. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2017]","start":110944285,"end":111227361,"strand":1,"description":"p21 (RAC1) activated kinase 3 [Source:HGNC Symbol;Acc:HGNC:8592]"}, {"versioned_ensembl_gene_id":"ENSG00000237414.2","gene_symbol":"AL365204.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23894990,"end":23898054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273374.1","gene_symbol":"AC069222.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99802699,"end":99806058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277608.1","gene_symbol":"AL365204.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23955760,"end":23956444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155287.10","gene_symbol":"SLC25A28","gene_name":"solute carrier family 25 member 28 [Source:HGNC Symbol;Acc:HGNC:23472]","synonyms":"MRS4L,MRS3/4","biotype":"protein_coding","ncbi_id":"81894","summary":null,"start":99610522,"end":99620609,"strand":-1,"description":"solute carrier family 25 member 28 [Source:HGNC Symbol;Acc:HGNC:23472]"}, {"versioned_ensembl_gene_id":"ENSG00000234084.1","gene_symbol":"AL049552.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135301568,"end":135307158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133519.12","gene_symbol":"ZDHHC8P1","gene_name":"zinc finger DHHC-type containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26461]","synonyms":"ZDHHC8P,FLJ31568","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"150244","summary":null,"start":23390606,"end":23402726,"strand":-1,"description":"zinc finger DHHC-type containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26461]"}, {"versioned_ensembl_gene_id":"ENSG00000213995.11","gene_symbol":"NAXD","gene_name":"NAD(P)HX dehydratase [Source:HGNC Symbol;Acc:HGNC:25576]","synonyms":"LP3298,FLJ10769,CARKD","biotype":"protein_coding","ncbi_id":"55739","summary":null,"start":110615460,"end":110639993,"strand":1,"description":"NAD(P)HX dehydratase [Source:HGNC Symbol;Acc:HGNC:25576]"}, {"versioned_ensembl_gene_id":"ENSG00000221909.2","gene_symbol":"FAM200A","gene_name":"family with sequence similarity 200 member A [Source:HGNC Symbol;Acc:HGNC:25401]","synonyms":"FLJ36794,DKFZp727G131,C7orf38","biotype":"protein_coding","ncbi_id":"221786","summary":"This gene encodes a protein of unknown function. The protein is weakly similar to transposase-like proteins in human and mouse. [provided by RefSeq, Jul 2008]","start":99546308,"end":99558536,"strand":-1,"description":"family with sequence similarity 200 member A [Source:HGNC Symbol;Acc:HGNC:25401]"}, {"versioned_ensembl_gene_id":"ENSG00000187860.10","gene_symbol":"CCDC157","gene_name":"coiled-coil domain containing 157 [Source:HGNC Symbol;Acc:HGNC:33854]","synonyms":null,"biotype":"protein_coding","ncbi_id":"550631","summary":null,"start":30356635,"end":30378658,"strand":1,"description":"coiled-coil domain containing 157 [Source:HGNC Symbol;Acc:HGNC:33854]"}, {"versioned_ensembl_gene_id":"ENSG00000144908.13","gene_symbol":"ALDH1L1","gene_name":"aldehyde dehydrogenase 1 family member L1 [Source:HGNC Symbol;Acc:HGNC:3978]","synonyms":"10-fTHF,FTHFD","biotype":"protein_coding","ncbi_id":"10840","summary":"The protein encoded by this gene catalyzes the conversion of 10-formyltetrahydrofolate, nicotinamide adenine dinucleotide phosphate (NADP+), and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family. Loss of function or expression of this gene is associated with decreased apoptosis, increased cell motility, and cancer progression. There is an antisense transcript that overlaps on the opposite strand with this gene locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":126103562,"end":126197994,"strand":-1,"description":"aldehyde dehydrogenase 1 family member L1 [Source:HGNC Symbol;Acc:HGNC:3978]"}, {"versioned_ensembl_gene_id":"ENSG00000135541.20","gene_symbol":"AHI1","gene_name":"Abelson helper integration site 1 [Source:HGNC Symbol;Acc:HGNC:21575]","synonyms":"ORF1,JBTS3,FLJ20069","biotype":"protein_coding","ncbi_id":"54806","summary":"This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]","start":135283532,"end":135497776,"strand":-1,"description":"Abelson helper integration site 1 [Source:HGNC Symbol;Acc:HGNC:21575]"}, {"versioned_ensembl_gene_id":"ENSG00000248409.1","gene_symbol":"AP000344.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23392771,"end":23393839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230292.5","gene_symbol":"NAALADL2-AS3","gene_name":"NAALADL2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:41014]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100862679","summary":null,"start":175079307,"end":175115242,"strand":-1,"description":"NAALADL2 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:41014]"}, {"versioned_ensembl_gene_id":"ENSG00000244219.6","gene_symbol":"TMEM225B","gene_name":"transmembrane protein 225B [Source:HGNC Symbol;Acc:HGNC:53075]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100289187","summary":null,"start":99598066,"end":99610813,"strand":1,"description":"transmembrane protein 225B [Source:HGNC Symbol;Acc:HGNC:53075]"}, {"versioned_ensembl_gene_id":"ENSG00000224728.1","gene_symbol":"IMPDH1P8","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33963]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"131961","summary":null,"start":15878047,"end":15879571,"strand":1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33963]"}, {"versioned_ensembl_gene_id":"ENSG00000270791.1","gene_symbol":"AC092474.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40758483,"end":40759050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186575.17","gene_symbol":"NF2","gene_name":"neurofibromin 2 [Source:HGNC Symbol;Acc:HGNC:7773]","synonyms":"SCH,merlin,BANF,ACN","biotype":"protein_coding","ncbi_id":"4771","summary":"This gene encodes a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that are thought to link cytoskeletal components with proteins in the cell membrane. This gene product has been shown to interact with cell-surface proteins, proteins involved in cytoskeletal dynamics and proteins involved in regulating ion transport. This gene is expressed at high levels during embryonic development; in adults, significant expression is found in Schwann cells, meningeal cells, lens and nerve. Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities. Two predominant isoforms and a number of minor isoforms are produced by alternatively spliced transcripts. [provided by RefSeq, Jul 2008]","start":29603556,"end":29698598,"strand":1,"description":"neurofibromin 2 [Source:HGNC Symbol;Acc:HGNC:7773]"}, {"versioned_ensembl_gene_id":"ENSG00000279883.1","gene_symbol":"AC010480.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":55484403,"end":55485086,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230497.2","gene_symbol":"EEF1B2P8","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421774","summary":null,"start":175059361,"end":175060031,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51455]"}, {"versioned_ensembl_gene_id":"ENSG00000214031.2","gene_symbol":"AC092474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40760104,"end":40761270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240695.1","gene_symbol":"AC117382.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136736500,"end":136737229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237661.1","gene_symbol":"AC092474.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40831844,"end":40832562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261175.5","gene_symbol":"LINC02188","gene_name":"long intergenic non-protein coding RNA 2188 [Source:HGNC Symbol;Acc:HGNC:53050]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724344","summary":null,"start":86722091,"end":86741059,"strand":1,"description":"long intergenic non-protein coding RNA 2188 [Source:HGNC Symbol;Acc:HGNC:53050]"}, {"versioned_ensembl_gene_id":"ENSG00000234928.1","gene_symbol":"LINC01659","gene_name":"long intergenic non-protein coding RNA 1659 [Source:HGNC Symbol;Acc:HGNC:52447]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929374","summary":null,"start":23433564,"end":23435071,"strand":1,"description":"long intergenic non-protein coding RNA 1659 [Source:HGNC Symbol;Acc:HGNC:52447]"}, {"versioned_ensembl_gene_id":"ENSG00000114054.13","gene_symbol":"PCCB","gene_name":"propionyl-CoA carboxylase beta subunit [Source:HGNC Symbol;Acc:HGNC:8654]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5096","summary":"The protein encoded by this gene is a subunit of the propionyl-CoA carboxylase (PCC) enzyme, which is involved in the catabolism of propionyl-CoA. PCC is a mitochondrial enzyme that probably acts as a dodecamer of six alpha subunits and six beta subunits. This gene encodes the beta subunit of PCC. Defects in this gene are a cause of propionic acidemia type II (PA-2). Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":136250306,"end":136337896,"strand":1,"description":"propionyl-CoA carboxylase beta subunit [Source:HGNC Symbol;Acc:HGNC:8654]"}, {"versioned_ensembl_gene_id":"ENSG00000132622.10","gene_symbol":"HSPA12B","gene_name":"heat shock protein family A (Hsp70) member 12B [Source:HGNC Symbol;Acc:HGNC:16193]","synonyms":"dJ1009E24.2,C20orf60","biotype":"protein_coding","ncbi_id":"116835","summary":"The protein encoded by this gene contains an atypical heat shock protein 70 (Hsp70) ATPase domain and is therefore a distant member of the mammalian Hsp70 family. This gene may be involved in susceptibility to atherosclerosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":3732667,"end":3753111,"strand":1,"description":"heat shock protein family A (Hsp70) member 12B [Source:HGNC Symbol;Acc:HGNC:16193]"}, {"versioned_ensembl_gene_id":"ENSG00000238222.3","gene_symbol":"MKRN4P","gene_name":"makorin ring finger protein 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:7115]","synonyms":"ZNF127L1,ZNF-Xp,RNF64,MKRNP5,MKRN4","biotype":"processed_pseudogene","ncbi_id":"7682","summary":null,"start":40834485,"end":40836005,"strand":1,"description":"makorin ring finger protein 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:7115]"}, {"versioned_ensembl_gene_id":"ENSG00000197847.12","gene_symbol":"SLC22A20","gene_name":"solute carrier family 22 member 20 [Source:HGNC Symbol;Acc:HGNC:29867]","synonyms":"Oat6,FLJ16331","biotype":"transcribed_unitary_pseudogene","ncbi_id":"440044","summary":null,"start":65213840,"end":65242757,"strand":1,"description":"solute carrier family 22 member 20 [Source:HGNC Symbol;Acc:HGNC:29867]"}, {"versioned_ensembl_gene_id":"ENSG00000249590.7","gene_symbol":"AC004832.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30409255,"end":30428990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272647.3","gene_symbol":"AC005020.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99558695,"end":99607810,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236464.1","gene_symbol":"LINC02559","gene_name":"long intergenic non-protein coding RNA 2559 [Source:HGNC Symbol;Acc:HGNC:53598]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372972","summary":null,"start":26161834,"end":26164303,"strand":1,"description":"long intergenic non-protein coding RNA 2559 [Source:HGNC Symbol;Acc:HGNC:53598]"}, {"versioned_ensembl_gene_id":"ENSG00000229770.1","gene_symbol":"AL022337.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26161910,"end":26163214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197343.10","gene_symbol":"ZNF655","gene_name":"zinc finger protein 655 [Source:HGNC Symbol;Acc:HGNC:30899]","synonyms":"VIK-1,VIK","biotype":"protein_coding","ncbi_id":"79027","summary":"This gene encodes a zinc finger protein. The zinc finger proteins are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":99558406,"end":99576453,"strand":1,"description":"zinc finger protein 655 [Source:HGNC Symbol;Acc:HGNC:30899]"}, {"versioned_ensembl_gene_id":"ENSG00000275031.2","gene_symbol":"METRNL","gene_name":"meteorin like, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:27584]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284207","summary":null,"start":83077507,"end":83097050,"strand":1,"description":"meteorin like, glial cell differentiation regulator [Source:HGNC Symbol;Acc:HGNC:27584]"}, {"versioned_ensembl_gene_id":"ENSG00000242114.5","gene_symbol":"MTFP1","gene_name":"mitochondrial fission process 1 [Source:HGNC Symbol;Acc:HGNC:26945]","synonyms":"MTP18,HSPC242","biotype":"protein_coding","ncbi_id":"51537","summary":"MTP18 is a mitochondrial protein and downstream target of the phosphatidylinositol 3-kinase (see PIK3CA, MIM 171834) signaling pathway that plays a role in cell viability and mitochondrial dynamics (Tondera et al., 2004 [PubMed 15155745]).[supplied by OMIM, Mar 2008]","start":30425530,"end":30429053,"strand":1,"description":"mitochondrial fission process 1 [Source:HGNC Symbol;Acc:HGNC:26945]"}, {"versioned_ensembl_gene_id":"ENSG00000143570.17","gene_symbol":"SLC39A1","gene_name":"solute carrier family 39 member 1 [Source:HGNC Symbol;Acc:HGNC:12876]","synonyms":"ZIRTL,ZIP1","biotype":"protein_coding","ncbi_id":"27173","summary":"This gene encodes a member of the zinc-iron permease family. The encoded protein is localized to the cell membrane and acts as a zinc uptake transporter. This gene has been linked to prostate cancer, breast cancer, and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":153959099,"end":153968184,"strand":-1,"description":"solute carrier family 39 member 1 [Source:HGNC Symbol;Acc:HGNC:12876]"}, {"versioned_ensembl_gene_id":"ENSG00000262468.5","gene_symbol":"LINC01569","gene_name":"long intergenic non-protein coding RNA 1569 [Source:HGNC Symbol;Acc:HGNC:51380]","synonyms":"TCONS_00024567","biotype":"lincRNA","ncbi_id":"100507501","summary":null,"start":4245825,"end":4253789,"strand":-1,"description":"long intergenic non-protein coding RNA 1569 [Source:HGNC Symbol;Acc:HGNC:51380]"}, {"versioned_ensembl_gene_id":"ENSG00000228355.1","gene_symbol":"BX322559.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45378201,"end":45379635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270606.1","gene_symbol":"AC025518.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8560471,"end":8560962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273796.1","gene_symbol":"BX322562.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45403809,"end":45404369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244604.1","gene_symbol":"AC025518.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8561230,"end":8561576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223883.1","gene_symbol":"LINC01707","gene_name":"long intergenic non-protein coding RNA 1707 [Source:HGNC Symbol;Acc:HGNC:52495]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378785","summary":null,"start":69055898,"end":69185003,"strand":1,"description":"long intergenic non-protein coding RNA 1707 [Source:HGNC Symbol;Acc:HGNC:52495]"}, {"versioned_ensembl_gene_id":"ENSG00000235446.1","gene_symbol":"AL512271.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69243372,"end":69249423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166579.15","gene_symbol":"NDEL1","gene_name":"nudE neurodevelopment protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:17620]","synonyms":"NUDEL,NDE2,NDE1L1,MITAP1","biotype":"protein_coding","ncbi_id":"81565","summary":"This gene encodes a coiled-coil protein that plays a role in multiple processes including cytoskeletal organization, cell signaling and neuron migration, outgrowth and maintenance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, Mar 2012]","start":8413131,"end":8490411,"strand":1,"description":"nudE neurodevelopment protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:17620]"}, {"versioned_ensembl_gene_id":"ENSG00000229639.1","gene_symbol":"LINC01758","gene_name":"long intergenic non-protein coding RNA 1758 [Source:HGNC Symbol;Acc:HGNC:52547]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378788","summary":null,"start":69433255,"end":69435409,"strand":1,"description":"long intergenic non-protein coding RNA 1758 [Source:HGNC Symbol;Acc:HGNC:52547]"}, {"versioned_ensembl_gene_id":"ENSG00000225552.1","gene_symbol":"NAALADL2-AS1","gene_name":"NAALADL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41016]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874245","summary":null,"start":175773145,"end":175776333,"strand":-1,"description":"NAALADL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41016]"}, {"versioned_ensembl_gene_id":"ENSG00000102225.15","gene_symbol":"CDK16","gene_name":"cyclin dependent kinase 16 [Source:HGNC Symbol;Acc:HGNC:8749]","synonyms":"PCTK1,PCTGAIRE,PCTAIRE1,PCTAIRE,FLJ16665","biotype":"protein_coding","ncbi_id":"5127","summary":"The protein encoded by this gene belongs to the cdc2/cdkx subfamily of the ser/thr family of protein kinases. It may play a role in signal transduction cascades in terminally differentiated cells; in exocytosis; and in transport of secretory cargo from the endoplasmic reticulum. This gene is thought to escape X inactivation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2009]","start":47217860,"end":47229997,"strand":1,"description":"cyclin dependent kinase 16 [Source:HGNC Symbol;Acc:HGNC:8749]"}, {"versioned_ensembl_gene_id":"ENSG00000260942.1","gene_symbol":"CAPN10-AS1","gene_name":"CAPN10 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48839]","synonyms":"locus959","biotype":"antisense_RNA","ncbi_id":"101752400","summary":null,"start":240582700,"end":240586699,"strand":-1,"description":"CAPN10 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48839]"}, {"versioned_ensembl_gene_id":"ENSG00000104237.7","gene_symbol":"RP1","gene_name":"RP1, axonemal microtubule associated [Source:HGNC Symbol;Acc:HGNC:10263]","synonyms":"ORP1,DCDC4A","biotype":"protein_coding","ncbi_id":"6101","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. Transcript variants resulted from an alternative promoter and alternative splicings have been found, which overlap the current reference sequence and has several exons upstream and downstream of the current reference sequence. However, the biological validity and full-length nature of some variants cannot be determined at this time.[provided by RefSeq, Sep 2010]","start":54554361,"end":54871720,"strand":1,"description":"RP1, axonemal microtubule associated [Source:HGNC Symbol;Acc:HGNC:10263]"}, {"versioned_ensembl_gene_id":"ENSG00000214192.3","gene_symbol":"UBE2V1P2","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730052","summary":null,"start":175718231,"end":175718670,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32648]"}, {"versioned_ensembl_gene_id":"ENSG00000236241.1","gene_symbol":"AC119744.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175675087,"end":175676801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283516.1","gene_symbol":"AC022167.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8881634,"end":8885351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243516.1","gene_symbol":"RPL12P40","gene_name":"ribosomal protein L12 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36439]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646898","summary":null,"start":37672689,"end":37673176,"strand":1,"description":"ribosomal protein L12 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36439]"}, {"versioned_ensembl_gene_id":"ENSG00000268566.5","gene_symbol":"AC100781.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38655209,"end":38687998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226779.1","gene_symbol":"NAALADL2-AS2","gene_name":"NAALADL2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41015]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874244","summary":null,"start":175234861,"end":175271096,"strand":-1,"description":"NAALADL2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41015]"}, {"versioned_ensembl_gene_id":"ENSG00000221944.6","gene_symbol":"TIGD1","gene_name":"tigger transposable element derived 1 [Source:HGNC Symbol;Acc:HGNC:14523]","synonyms":"EEYORE","biotype":"protein_coding","ncbi_id":"200765","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":232547968,"end":232550592,"strand":-1,"description":"tigger transposable element derived 1 [Source:HGNC Symbol;Acc:HGNC:14523]"}, {"versioned_ensembl_gene_id":"ENSG00000136383.6","gene_symbol":"ALPK3","gene_name":"alpha kinase 3 [Source:HGNC Symbol;Acc:HGNC:17574]","synonyms":"Midori,MAK,KIAA1330","biotype":"protein_coding","ncbi_id":"57538","summary":null,"start":84816680,"end":84873482,"strand":1,"description":"alpha kinase 3 [Source:HGNC Symbol;Acc:HGNC:17574]"}, {"versioned_ensembl_gene_id":"ENSG00000260795.1","gene_symbol":"AC093519.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86906175,"end":86906472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237126.8","gene_symbol":"AC073254.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":232580948,"end":232611971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144224.16","gene_symbol":"UBXN4","gene_name":"UBX domain protein 4 [Source:HGNC Symbol;Acc:HGNC:14860]","synonyms":"UBXDC1,UBXD2,KIAA0242","biotype":"protein_coding","ncbi_id":"23190","summary":"UBXD2 is an integral membrane protein of the endoplasmic reticulum (ER) that binds valosin-containing protein (VCP; MIM 601023) and promotes ER-associated protein degradation (ERAD) (Liang et al., 2006 [PubMed 16968747]).[supplied by OMIM, Mar 2008]","start":135741619,"end":135785055,"strand":1,"description":"UBX domain protein 4 [Source:HGNC Symbol;Acc:HGNC:14860]"}, {"versioned_ensembl_gene_id":"ENSG00000169021.5","gene_symbol":"UQCRFS1","gene_name":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:12587]","synonyms":"UQCR5,RISP,RIS1,RIP1","biotype":"protein_coding","ncbi_id":"7386","summary":null,"start":29205321,"end":29213541,"strand":-1,"description":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:12587]"}, {"versioned_ensembl_gene_id":"ENSG00000275880.1","gene_symbol":"AL139385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110613082,"end":110616353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267498.1","gene_symbol":"AC007786.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29213235,"end":29215815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231003.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"C6orf25,G6b-B,G6b,NG31","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31709355,"end":31717471,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000115468.11","gene_symbol":"EFHD1","gene_name":"EF-hand domain family member D1 [Source:HGNC Symbol;Acc:HGNC:29556]","synonyms":"FLJ13612","biotype":"protein_coding","ncbi_id":"80303","summary":"This gene encodes a member of the EF-hand super family of calcium binding proteins, which are involved in a variety of cellular processes including mitosis, synaptic transmission, and cytoskeletal rearrangement. The protein encoded by this gene is composed of an N-terminal disordered region, proline-rich elements, two EF-hands, and a C-terminal coiled-coil domain. This protein has been shown to associate with the mitochondrial inner membrane, and in HeLa cells, acts as a novel mitochondrial calcium ion sensor for mitochondrial flash activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":232606057,"end":232682781,"strand":1,"description":"EF-hand domain family member D1 [Source:HGNC Symbol;Acc:HGNC:29556]"}, {"versioned_ensembl_gene_id":"ENSG00000232190.2","gene_symbol":"LINC02181","gene_name":"long intergenic non-protein coding RNA 2181 [Source:HGNC Symbol;Acc:HGNC:53043]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440390","summary":null,"start":87057784,"end":87063991,"strand":1,"description":"long intergenic non-protein coding RNA 2181 [Source:HGNC Symbol;Acc:HGNC:53043]"}, {"versioned_ensembl_gene_id":"ENSG00000261363.2","gene_symbol":"AC106745.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87066705,"end":87069752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100003.17","gene_symbol":"SEC14L2","gene_name":"SEC14 like lipid binding 2 [Source:HGNC Symbol;Acc:HGNC:10699]","synonyms":"TAP1,TAP,SPF,KIAA1658,KIAA1186,C22orf6","biotype":"protein_coding","ncbi_id":"23541","summary":"This gene encodes a cytosolic protein which belongs to a family of lipid-binding proteins including Sec14p, alpha-tocopherol transfer protein, and cellular retinol-binding protein. The encoded protein stimulates squalene monooxygenase which is a downstream enzyme in the cholesterol biosynthetic pathway. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008]","start":30396857,"end":30425317,"strand":1,"description":"SEC14 like lipid binding 2 [Source:HGNC Symbol;Acc:HGNC:10699]"}, {"versioned_ensembl_gene_id":"ENSG00000260475.1","gene_symbol":"AL353719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99621055,"end":99621918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276251.1","gene_symbol":"AC007786.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29220864,"end":29221666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240288.7","gene_symbol":"GHRLOS","gene_name":"ghrelin opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:33885]","synonyms":"NCRNA00068,GHRL-AS1","biotype":"antisense_RNA","ncbi_id":"100126793","summary":"This gene is an antisense gene of the ghrelin/obestatin prepropeptide gene. Alternatively spliced transcript variants have been identified and they may function as non-coding regulatory RNAs. [provided by RefSeq, Jan 2013]","start":10285754,"end":10293449,"strand":1,"description":"ghrelin opposite strand/antisense RNA [Source:HGNC Symbol;Acc:HGNC:33885]"}, {"versioned_ensembl_gene_id":"ENSG00000229278.1","gene_symbol":"AL133353.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99651989,"end":99653905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197641.11","gene_symbol":"SERPINB13","gene_name":"serpin family B member 13 [Source:HGNC Symbol;Acc:HGNC:8944]","synonyms":"PI13,hurpin,HUR7,headpin","biotype":"protein_coding","ncbi_id":"5275","summary":"The protein encoded by this gene is a member of the serpin family of serine protease inhibitors. The encoded protein inhibits the activity of cathepsin K and is itself transcriptionally repressed by RUNX1. This gene is downregulated in many types of cancer. [provided by RefSeq, Jan 2017]","start":63586989,"end":63604639,"strand":1,"description":"serpin family B member 13 [Source:HGNC Symbol;Acc:HGNC:8944]"}, {"versioned_ensembl_gene_id":"ENSG00000226875.1","gene_symbol":"ZNF877P","gene_name":"zinc finger protein 877, pseudogene [Source:HGNC Symbol;Acc:HGNC:38697]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873811","summary":null,"start":21265854,"end":21266465,"strand":1,"description":"zinc finger protein 877, pseudogene [Source:HGNC Symbol;Acc:HGNC:38697]"}, {"versioned_ensembl_gene_id":"ENSG00000231177.4","gene_symbol":"LINC00852","gene_name":"long intergenic non-protein coding RNA 852 [Source:HGNC Symbol;Acc:HGNC:29904]","synonyms":"NAG73,GHRLOS2,GHRL-AS2,C3orf42","biotype":"antisense_RNA","ncbi_id":"84657","summary":null,"start":10284419,"end":10285746,"strand":1,"description":"long intergenic non-protein coding RNA 852 [Source:HGNC Symbol;Acc:HGNC:29904]"}, {"versioned_ensembl_gene_id":"ENSG00000271410.1","gene_symbol":"AC020728.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55356308,"end":55357523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067113.16","gene_symbol":"PLPP1","gene_name":"phospholipid phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:9228]","synonyms":"PPAP2A,PAP-2a,LPP1","biotype":"protein_coding","ncbi_id":"8611","summary":"The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in synthesis of glycerolipids and in phospholipase D-mediated signal transduction. This enzyme is an integral membrane glycoprotein that plays a role in the hydrolysis and uptake of lipids from extracellular space. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":55424854,"end":55535050,"strand":-1,"description":"phospholipid phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:9228]"}, {"versioned_ensembl_gene_id":"ENSG00000157017.15","gene_symbol":"GHRL","gene_name":"ghrelin and obestatin prepropeptide [Source:HGNC Symbol;Acc:HGNC:18129]","synonyms":"obestatin,MTLRP,ghrelin","biotype":"protein_coding","ncbi_id":"51738","summary":"This gene encodes the ghrelin-obestatin preproprotein that is cleaved to yield two peptides, ghrelin and obestatin. Ghrelin is a powerful appetite stimulant and plays an important role in energy homeostasis. Its secretion is initiated when the stomach is empty, whereupon it binds to the growth hormone secretagogue receptor in the hypothalamus which results in the secretion of growth hormone (somatotropin). Ghrelin is thought to regulate multiple activities, including hunger, reward perception via the mesolimbic pathway, gastric acid secretion, gastrointestinal motility, and pancreatic glucose-stimulated insulin secretion. It was initially proposed that obestatin plays an opposing role to ghrelin by promoting satiety and thus decreasing food intake, but this action is still debated. Recent reports suggest multiple metabolic roles for obestatin, including regulating adipocyte function and glucose metabolism. Alternative splicing results in multiple transcript variants. In addition, antisense transcripts for this gene have been identified and may potentially regulate ghrelin-obestatin preproprotein expression. [provided by RefSeq, Nov 2014]","start":10285675,"end":10292947,"strand":-1,"description":"ghrelin and obestatin prepropeptide [Source:HGNC Symbol;Acc:HGNC:18129]"}, {"versioned_ensembl_gene_id":"ENSG00000261275.1","gene_symbol":"AC092447.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56493124,"end":56497285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230154.1","gene_symbol":"AC018463.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11308025,"end":11308941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231504.1","gene_symbol":"NMD3P2","gene_name":"NMD3 ribosome export adaptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37820]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100286929","summary":null,"start":56502284,"end":56503044,"strand":-1,"description":"NMD3 ribosome export adaptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37820]"}, {"versioned_ensembl_gene_id":"ENSG00000232695.1","gene_symbol":"ELOCP17","gene_name":"elongin C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38153]","synonyms":"TCEB1P17","biotype":"processed_pseudogene","ncbi_id":"100462879","summary":null,"start":25860943,"end":25861268,"strand":1,"description":"elongin C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38153]"}, {"versioned_ensembl_gene_id":"ENSG00000186470.13","gene_symbol":"BTN3A2","gene_name":"butyrophilin subfamily 3 member A2 [Source:HGNC Symbol;Acc:HGNC:1139]","synonyms":"BTN3.2","biotype":"protein_coding","ncbi_id":"11118","summary":"This gene encodes a member of the immunoglobulin superfamily, which resides in the juxta-telomeric region of the major histocompatability class 1 locus and is clustered with the other family members on chromosome 6. The encoded protein may be involved in the adaptive immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]","start":26365159,"end":26378320,"strand":1,"description":"butyrophilin subfamily 3 member A2 [Source:HGNC Symbol;Acc:HGNC:1139]"}, {"versioned_ensembl_gene_id":"ENSG00000235511.1","gene_symbol":"OFD1P18Y","gene_name":"OFD1 pseudogene 18, Y-linked [Source:HGNC Symbol;Acc:HGNC:2589]","synonyms":"OFD1PY18,OFD1P18,CYorf1,71-7A2","biotype":"unprocessed_pseudogene","ncbi_id":"10751","summary":null,"start":25871931,"end":25898653,"strand":-1,"description":"OFD1 pseudogene 18, Y-linked [Source:HGNC Symbol;Acc:HGNC:2589]"}, {"versioned_ensembl_gene_id":"ENSG00000223740.1","gene_symbol":"AC092447.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56525428,"end":56526113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270082.1","gene_symbol":"AC010531.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87326987,"end":87327584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242795.2","gene_symbol":"AC007849.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":169613510,"end":169623951,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140941.12","gene_symbol":"MAP1LC3B","gene_name":"microtubule associated protein 1 light chain 3 beta [Source:HGNC Symbol;Acc:HGNC:13352]","synonyms":"ATG8F","biotype":"protein_coding","ncbi_id":"81631","summary":" The product of this gene is a subunit of neuronal microtubule-associated MAP1A and MAP1B proteins, which are involved in microtubule assembly and important for neurogenesis. Studies on the rat homolog implicate a role for this gene in autophagy, a process that involves the bulk degradation of cytoplasmic component. [provided by RefSeq, Jul 2008]","start":87383995,"end":87404779,"strand":1,"description":"microtubule associated protein 1 light chain 3 beta [Source:HGNC Symbol;Acc:HGNC:13352]"}, {"versioned_ensembl_gene_id":"ENSG00000233288.1","gene_symbol":"AC092447.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56534230,"end":56538130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232914.1","gene_symbol":"TRAPPC2P4","gene_name":"trafficking protein particle complex 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10713]","synonyms":"SEDLP4","biotype":"unprocessed_pseudogene","ncbi_id":"27194","summary":null,"start":25904518,"end":25907250,"strand":1,"description":"trafficking protein particle complex 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10713]"}, {"versioned_ensembl_gene_id":"ENSG00000241479.1","gene_symbol":"AC074033.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169447867,"end":169477052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224947.1","gene_symbol":"VN1R25P","gene_name":"vomeronasal 1 receptor 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:37345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312782","summary":null,"start":56559221,"end":56559958,"strand":1,"description":"vomeronasal 1 receptor 25 pseudogene [Source:HGNC Symbol;Acc:HGNC:37345]"}, {"versioned_ensembl_gene_id":"ENSG00000231557.1","gene_symbol":"AC020718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":198882573,"end":199071791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213650.3","gene_symbol":"AC092447.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56567906,"end":56568858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230407.1","gene_symbol":"AC018717.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199108584,"end":199110088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112619.7","gene_symbol":"PRPH2","gene_name":"peripherin 2 [Source:HGNC Symbol;Acc:HGNC:9942]","synonyms":"TSPAN22,RP7,RDS,rd2,CACD2","biotype":"protein_coding","ncbi_id":"5961","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic. [provided by RefSeq, Jul 2008]","start":42696600,"end":42722574,"strand":-1,"description":"peripherin 2 [Source:HGNC Symbol;Acc:HGNC:9942]"}, {"versioned_ensembl_gene_id":"ENSG00000229767.9","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"CD167,NEP,PTK3A,CAK,EDDR1,NTRK4,RTK6","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30949136,"end":30953340,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000213774.3","gene_symbol":"AC010904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7324748,"end":7325062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073464.11","gene_symbol":"CLCN4","gene_name":"chloride voltage-gated channel 4 [Source:HGNC Symbol;Acc:HGNC:2022]","synonyms":"CLC4,ClC-4","biotype":"protein_coding","ncbi_id":"1183","summary":"The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. Chloride channel 4 has an evolutionary conserved CpG island and is conserved in both mouse and hamster. This gene is mapped in close proximity to APXL (Apical protein Xenopus laevis-like) and OA1 (Ocular albinism type I), which are both located on the human X chromosome at band p22.3. The physiological role of chloride channel 4 remains unknown but may contribute to the pathogenesis of neuronal disorders. Alternate splicing results in two transcript variants that encode different proteins. [provided by RefSeq, Mar 2012]","start":10156945,"end":10237660,"strand":1,"description":"chloride voltage-gated channel 4 [Source:HGNC Symbol;Acc:HGNC:2022]"}, {"versioned_ensembl_gene_id":"ENSG00000250853.1","gene_symbol":"RNF138P1","gene_name":"ring finger protein 138 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"379013","summary":null,"start":55530156,"end":55530701,"strand":-1,"description":"ring finger protein 138 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30342]"}, {"versioned_ensembl_gene_id":"ENSG00000258220.1","gene_symbol":"LINC02424","gene_name":"long intergenic non-protein coding RNA 2424 [Source:HGNC Symbol;Acc:HGNC:53354]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369860","summary":null,"start":78326680,"end":78359746,"strand":-1,"description":"long intergenic non-protein coding RNA 2424 [Source:HGNC Symbol;Acc:HGNC:53354]"}, {"versioned_ensembl_gene_id":"ENSG00000232983.2","gene_symbol":"AL160270.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34546524,"end":34546996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226570.2","gene_symbol":"AL450304.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182955390,"end":182956148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135930.13","gene_symbol":"EIF4E2","gene_name":"eukaryotic translation initiation factor 4E family member 2 [Source:HGNC Symbol;Acc:HGNC:3293]","synonyms":"IF4e,EIF4EL3,4EHP","biotype":"protein_coding","ncbi_id":"9470","summary":null,"start":232550052,"end":232583644,"strand":1,"description":"eukaryotic translation initiation factor 4E family member 2 [Source:HGNC Symbol;Acc:HGNC:3293]"}, {"versioned_ensembl_gene_id":"ENSG00000280770.1","gene_symbol":"AC216281.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3427276,"end":3427885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257879.1","gene_symbol":"AC130415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78426826,"end":78442952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176855.11","gene_symbol":"KRT18P28","gene_name":"keratin 18 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:33397]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343326","summary":null,"start":182959074,"end":182960405,"strand":-1,"description":"keratin 18 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:33397]"}, {"versioned_ensembl_gene_id":"ENSG00000274891.3","gene_symbol":"TRAPPC12","gene_name":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]","synonyms":"TTC15,TTC-15,CGI-87","biotype":"protein_coding","ncbi_id":"51112","summary":null,"start":3401777,"end":3486461,"strand":1,"description":"trafficking protein particle complex 12 [Source:HGNC Symbol;Acc:HGNC:24284]"}, {"versioned_ensembl_gene_id":"ENSG00000257165.5","gene_symbol":"AC079362.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78448995,"end":78540675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232421.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30712452,"end":30717677,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000258084.5","gene_symbol":"AC128707.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78352519,"end":78483019,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144476.5","gene_symbol":"ACKR3","gene_name":"atypical chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:23692]","synonyms":"RDC1,GPR159,CXCR7,CMKOR1","biotype":"protein_coding","ncbi_id":"57007","summary":"This gene encodes a member of the G-protein coupled receptor family. Although this protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP), it is now considered to be an orphan receptor, in that its endogenous ligand has not been identified. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas. [provided by RefSeq, Jul 2008]","start":236567787,"end":236582358,"strand":1,"description":"atypical chemokine receptor 3 [Source:HGNC Symbol;Acc:HGNC:23692]"}, {"versioned_ensembl_gene_id":"ENSG00000100316.15","gene_symbol":"RPL3","gene_name":"ribosomal protein L3 [Source:HGNC Symbol;Acc:HGNC:10332]","synonyms":"L3","biotype":"protein_coding","ncbi_id":"6122","summary":"Ribosomes, the complexes that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L3P family of ribosomal proteins and it is located in the cytoplasm. The protein can bind to the HIV-1 TAR mRNA, and it has been suggested that the protein contributes to tat-mediated transactivation. This gene is co-transcribed with several small nucleolar RNA genes, which are located in several of this gene's introns. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":39312882,"end":39320389,"strand":-1,"description":"ribosomal protein L3 [Source:HGNC Symbol;Acc:HGNC:10332]"}, {"versioned_ensembl_gene_id":"ENSG00000224698.1","gene_symbol":"AL390038.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108420689,"end":108433184,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076321.10","gene_symbol":"KLHL20","gene_name":"kelch like family member 20 [Source:HGNC Symbol;Acc:HGNC:25056]","synonyms":"KLEIP,KHLHX","biotype":"protein_coding","ncbi_id":"27252","summary":"The protein encoded by this gene is a member of the kelch family of proteins, which is characterized by a 44-56 amino acid repeat motif. The kelch motif appears in many different polypeptide contexts and contains multiple potential protein-protein contact sites. Members of this family are present both throughout the cell and extracellularly, with diverse activities. [provided by RefSeq, Jul 2008]","start":173714941,"end":173786702,"strand":1,"description":"kelch like family member 20 [Source:HGNC Symbol;Acc:HGNC:25056]"}, {"versioned_ensembl_gene_id":"ENSG00000243967.4","gene_symbol":"NBPF5P","gene_name":"NBPF member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:24491]","synonyms":"NBPF5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100507044","summary":null,"start":108375838,"end":108410814,"strand":1,"description":"NBPF member 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:24491]"}, {"versioned_ensembl_gene_id":"ENSG00000235051.3","gene_symbol":"AL357497.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10881780,"end":10884349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230854.1","gene_symbol":"USP9YP20","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38767]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480717","summary":null,"start":25923388,"end":25929826,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38767]"}, {"versioned_ensembl_gene_id":"ENSG00000264515.5","gene_symbol":"AC011474.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29287011,"end":29525752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103264.17","gene_symbol":"FBXO31","gene_name":"F-box protein 31 [Source:HGNC Symbol;Acc:HGNC:16510]","synonyms":"MGC15419,FBXO14,Fbx31,FBX14","biotype":"protein_coding","ncbi_id":"79791","summary":"This gene is a member of the F-box family. Members are classified into three classes according to the substrate interaction domain, FBW for WD40 repeats, FBL for leucing-rich repeats, and FBXO for other domains. This protein, classified into the last category because of the lack of a recognizable substrate binding domain, has been proposed to be a component of the SCF ubiquitination complex. It is thought to bind and recruit substrate for ubiquitination and degradation. This protein may have a role in regulating the cell cycle as well as dendrite growth and neuronal migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":87326987,"end":87392142,"strand":-1,"description":"F-box protein 31 [Source:HGNC Symbol;Acc:HGNC:16510]"}, {"versioned_ensembl_gene_id":"ENSG00000282632.1","gene_symbol":"AC113211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37803402,"end":37807292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111837.11","gene_symbol":"MAK","gene_name":"male germ cell associated kinase [Source:HGNC Symbol;Acc:HGNC:6816]","synonyms":"RP62,dJ417M14.2","biotype":"protein_coding","ncbi_id":"4117","summary":"The product of this gene is a serine/threonine protein kinase related to kinases involved in cell cycle regulation. Studies of the mouse and rat homologs have localized the kinase to the chromosomes during meiosis in spermatogenesis, specifically to the synaptonemal complex that exists while homologous chromosomes are paired. Mutations in this gene have been associated with ciliary defects resulting in retinitis pigmentosa 62. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":10762723,"end":10838555,"strand":-1,"description":"male germ cell associated kinase [Source:HGNC Symbol;Acc:HGNC:6816]"}, {"versioned_ensembl_gene_id":"ENSG00000238118.1","gene_symbol":"SLC25A24P2","gene_name":"SLC25A24 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48934]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422608","summary":null,"start":108383736,"end":108421295,"strand":-1,"description":"SLC25A24 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48934]"}, {"versioned_ensembl_gene_id":"ENSG00000230399.1","gene_symbol":"RBBP8P1","gene_name":"RB binding protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39583]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420552","summary":null,"start":118632375,"end":118634218,"strand":-1,"description":"RB binding protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39583]"}, {"versioned_ensembl_gene_id":"ENSG00000183036.10","gene_symbol":"PCP4","gene_name":"Purkinje cell protein 4 [Source:HGNC Symbol;Acc:HGNC:8742]","synonyms":"PEP-19","biotype":"protein_coding","ncbi_id":"5121","summary":null,"start":39867317,"end":39929397,"strand":1,"description":"Purkinje cell protein 4 [Source:HGNC Symbol;Acc:HGNC:8742]"}, {"versioned_ensembl_gene_id":"ENSG00000229353.10","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"XB,TNXB2,XBS,TNXB1,TNXBS","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31998796,"end":32043729,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000228578.1","gene_symbol":"TUBB1P2","gene_name":"tubulin beta 1 class VI pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23981]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"140004","summary":null,"start":17516836,"end":17519038,"strand":-1,"description":"tubulin beta 1 class VI pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23981]"}, {"versioned_ensembl_gene_id":"ENSG00000082929.8","gene_symbol":"LINC01587","gene_name":"long intergenic non-protein coding RNA 1587 [Source:HGNC Symbol;Acc:HGNC:13716]","synonyms":"C4orf6,aC1","biotype":"processed_transcript","ncbi_id":"10141","summary":"This gene is expressed in neuroblastoma; however, the function of this gene is not yet determined. [provided by RefSeq, Jul 2008]","start":5524569,"end":5527801,"strand":1,"description":"long intergenic non-protein coding RNA 1587 [Source:HGNC Symbol;Acc:HGNC:13716]"}, {"versioned_ensembl_gene_id":"ENSG00000107447.7","gene_symbol":"DNTT","gene_name":"DNA nucleotidylexotransferase [Source:HGNC Symbol;Acc:HGNC:2983]","synonyms":"TDT","biotype":"protein_coding","ncbi_id":"1791","summary":"This gene is a member of the DNA polymerase type-X family and encodes a template-independent DNA polymerase that catalyzes the addition of deoxynucleotides to the 3'-hydroxyl terminus of oligonucleotide primers. In vivo, the encoded protein is expressed in a restricted population of normal and malignant pre-B and pre-T lymphocytes during early differentiation, where it generates antigen receptor diversity by synthesizing non-germ line elements (N-regions) at the junctions of rearranged Ig heavy chain and T cell receptor gene segments. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]","start":96304396,"end":96338564,"strand":1,"description":"DNA nucleotidylexotransferase [Source:HGNC Symbol;Acc:HGNC:2983]"}, {"versioned_ensembl_gene_id":"ENSG00000196151.10","gene_symbol":"WDSUB1","gene_name":"WD repeat, sterile alpha motif and U-box domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26697]","synonyms":"WDSAM1,UBOX6,FLJ36175","biotype":"protein_coding","ncbi_id":"151525","summary":null,"start":159235793,"end":159286799,"strand":-1,"description":"WD repeat, sterile alpha motif and U-box domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26697]"}, {"versioned_ensembl_gene_id":"ENSG00000226112.1","gene_symbol":"FCF1P4","gene_name":"FCF1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480799","summary":null,"start":111169221,"end":111169403,"strand":1,"description":"FCF1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44616]"}, {"versioned_ensembl_gene_id":"ENSG00000177414.13","gene_symbol":"UBE2U","gene_name":"ubiquitin conjugating enzyme E2 U (putative) [Source:HGNC Symbol;Acc:HGNC:28559]","synonyms":"MGC35130","biotype":"protein_coding","ncbi_id":"148581","summary":null,"start":64203627,"end":64267368,"strand":1,"description":"ubiquitin conjugating enzyme E2 U (putative) [Source:HGNC Symbol;Acc:HGNC:28559]"}, {"versioned_ensembl_gene_id":"ENSG00000282734.1","gene_symbol":"AF067845.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1296034,"end":1302607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233649.1","gene_symbol":"CR759784.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31960233,"end":31960526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259459.5","gene_symbol":"AC087525.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63390136,"end":63438320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230885.9","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTN6,BTNL11","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29656505,"end":29671893,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000276243.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000143578.15","gene_symbol":"CREB3L4","gene_name":"cAMP responsive element binding protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:18854]","synonyms":"CREB4,CREB3,ATCE1,AIbZIP,hJAL","biotype":"protein_coding","ncbi_id":"148327","summary":"This gene encodes a CREB (cAMP responsive element binding) protein with a transmembrane domain which localizes it to the ER membrane. The encoded protein is a transcriptional activator which contains a dimerization domain, and this protein may function in a number of processing pathways including protein processing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":153967534,"end":153974363,"strand":1,"description":"cAMP responsive element binding protein 3 like 4 [Source:HGNC Symbol;Acc:HGNC:18854]"}, {"versioned_ensembl_gene_id":"ENSG00000259268.1","gene_symbol":"AC007950.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63456294,"end":63469351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278211.4","gene_symbol":"TRIM69","gene_name":"tripartite motif containing 69 [Source:HGNC Symbol;Acc:HGNC:17857]","synonyms":"TRIMLESS,Trif,RNF36","biotype":"protein_coding","ncbi_id":"140691","summary":"This gene encodes a member of the RING-B-box-coiled-coil (RBCC) family and encodes a protein with an N-terminal RING finger motif, a PRY domain and a C-terminal SPRY domain. The mouse ortholog of this gene is specifically expressed in germ cells at the round spermatid stages during spermatogenesis and, when overexpressed, induces apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":44729020,"end":44767863,"strand":1,"description":"tripartite motif containing 69 [Source:HGNC Symbol;Acc:HGNC:17857]"}, {"versioned_ensembl_gene_id":"ENSG00000234716.1","gene_symbol":"AC092447.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56577848,"end":56578866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276001.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000213067.2","gene_symbol":"AC092447.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56597379,"end":56598342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271047.1","gene_symbol":"AC092447.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56603410,"end":56603553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234280.6","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32241266,"end":32320157,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000229909.1","gene_symbol":"TRIM60P16","gene_name":"tripartite motif containing 60 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38488]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420412","summary":null,"start":56631739,"end":56632727,"strand":-1,"description":"tripartite motif containing 60 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38488]"}, {"versioned_ensembl_gene_id":"ENSG00000250261.1","gene_symbol":"CCDC74BP1","gene_name":"coiled-coil domain containing 74B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51917]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996538","summary":null,"start":20587496,"end":20592218,"strand":-1,"description":"coiled-coil domain containing 74B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51917]"}, {"versioned_ensembl_gene_id":"ENSG00000228303.1","gene_symbol":"AC095038.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56638943,"end":56650696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225591.2","gene_symbol":"BX248409.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":173741674,"end":173741928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087274.16","gene_symbol":"ADD1","gene_name":"adducin 1 [Source:HGNC Symbol;Acc:HGNC:243]","synonyms":null,"biotype":"protein_coding","ncbi_id":"118","summary":"Adducins are a family of cytoskeletal proteins encoded by three genes (alpha, beta, and gamma). Adducin acts as a heterodimer of the related alpha, beta, or gamma subunits. The protein encoded by this gene represents the alpha subunit. Alpha- and beta-adducin include a protease-resistant N-terminal region and a protease-sensitive, hydrophilic C-terminal region. Adducin binds with high affinity to Ca(2+)/calmodulin and is a substrate for protein kinases A and C. [provided by RefSeq, Aug 2017]","start":2843857,"end":2930076,"strand":1,"description":"adducin 1 [Source:HGNC Symbol;Acc:HGNC:243]"}, {"versioned_ensembl_gene_id":"ENSG00000277174.1","gene_symbol":"AC095038.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56685036,"end":56687366,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213435.3","gene_symbol":"ATP6V0CP3","gene_name":"ATPase H+ transporting V0 subunit c pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:40001]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442211","summary":null,"start":42727234,"end":42727700,"strand":1,"description":"ATPase H+ transporting V0 subunit c pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:40001]"}, {"versioned_ensembl_gene_id":"ENSG00000243705.1","gene_symbol":"AC010531.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87268185,"end":87268337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274588.1","gene_symbol":"DGKK","gene_name":"diacylglycerol kinase kappa [Source:HGNC Symbol;Acc:HGNC:32395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"139189","summary":"The protein encoded by this gene is an enzyme that phosphorylates diacylglycerol, converting it to phosphatidic acid. The encoded protein is a membrane protein and is inhibited by hydrogen peroxide. Variations in this gene have been associated with hypospadias. [provided by RefSeq, Mar 2011]","start":50365409,"end":50470738,"strand":-1,"description":"diacylglycerol kinase kappa [Source:HGNC Symbol;Acc:HGNC:32395]"}, {"versioned_ensembl_gene_id":"ENSG00000282879.1","gene_symbol":"AC095038.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56736396,"end":56736590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261095.1","gene_symbol":"AC136285.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87212122,"end":87226430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260128.6","gene_symbol":"ULK4P2","gene_name":"ULK4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15776]","synonyms":"FAM7A2,D-X","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288380","summary":null,"start":30572738,"end":30600647,"strand":1,"description":"ULK4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15776]"}, {"versioned_ensembl_gene_id":"ENSG00000242551.2","gene_symbol":"POU5F1P6","gene_name":"POU class 5 homeobox 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33312]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100009668","summary":null,"start":128674735,"end":128677005,"strand":-1,"description":"POU class 5 homeobox 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33312]"}, {"versioned_ensembl_gene_id":"ENSG00000277253.1","gene_symbol":"AC118758.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56805336,"end":56808148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280419.1","gene_symbol":"AC010531.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87296949,"end":87297633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163902.11","gene_symbol":"RPN1","gene_name":"ribophorin I [Source:HGNC Symbol;Acc:HGNC:10381]","synonyms":"OST1","biotype":"protein_coding","ncbi_id":"6184","summary":"This gene encodes a type I integral membrane protein found only in the rough endoplasmic reticulum. The encoded protein is part of an N-oligosaccharyl transferase complex that links high mannose oligosaccharides to asparagine residues found in the Asn-X-Ser/Thr consensus motif of nascent polypeptide chains. This protein forms part of the regulatory subunit of the 26S proteasome and may mediate binding of ubiquitin-like domains to this proteasome. [provided by RefSeq, Jul 2008]","start":128619970,"end":128681075,"strand":-1,"description":"ribophorin I [Source:HGNC Symbol;Acc:HGNC:10381]"}, {"versioned_ensembl_gene_id":"ENSG00000260456.6","gene_symbol":"C16orf95","gene_name":"chromosome 16 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:40033]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506581","summary":null,"start":87083562,"end":87317420,"strand":-1,"description":"chromosome 16 open reading frame 95 [Source:HGNC Symbol;Acc:HGNC:40033]"}, {"versioned_ensembl_gene_id":"ENSG00000171208.9","gene_symbol":"NETO2","gene_name":"neuropilin and tolloid like 2 [Source:HGNC Symbol;Acc:HGNC:14644]","synonyms":"NEOT2,FLJ10430","biotype":"protein_coding","ncbi_id":"81831","summary":"This gene encodes a predicted transmembrane protein containing two extracellular CUB domains followed by a low-density lipoprotein class A (LDLa) domain. A similar gene in rats encodes a protein that modulates glutamate signaling in the brain by regulating kainate receptor function. Expression of this gene may be a biomarker for proliferating infantile hemangiomas. A pseudogene of this gene is located on the long arm of chromosome 8. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":47077703,"end":47143997,"strand":-1,"description":"neuropilin and tolloid like 2 [Source:HGNC Symbol;Acc:HGNC:14644]"}, {"versioned_ensembl_gene_id":"ENSG00000231275.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32273814,"end":32274773,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000276651.1","gene_symbol":"AC007950.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63500737,"end":63503083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229418.2","gene_symbol":"AL136181.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96292685,"end":96306695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235925.3","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"G6c,C6orf24,NG24","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31709409,"end":31712606,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000226353.1","gene_symbol":"TAF9P1","gene_name":"TATA-box binding protein associated factor 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360002","summary":null,"start":17628513,"end":17629402,"strand":1,"description":"TATA-box binding protein associated factor 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31743]"}, {"versioned_ensembl_gene_id":"ENSG00000185758.8","gene_symbol":"CLDN24","gene_name":"claudin 24 [Source:HGNC Symbol;Acc:HGNC:37200]","synonyms":"CLDN21","biotype":"protein_coding","ncbi_id":"100132463","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is 75% identical to the mouse homolog. This gene is upstream of the CLDN22 gene, which overlaps the WWC2 gene on the opposite strand in the genome.[provided by RefSeq, Aug 2010]","start":183321764,"end":183322426,"strand":-1,"description":"claudin 24 [Source:HGNC Symbol;Acc:HGNC:37200]"}, {"versioned_ensembl_gene_id":"ENSG00000250292.1","gene_symbol":"AC093844.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183380345,"end":183381705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049249.8","gene_symbol":"TNFRSF9","gene_name":"TNF receptor superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:11924]","synonyms":"ILA,CD137,4-1BB","biotype":"protein_coding","ncbi_id":"3604","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contributes to the clonal expansion, survival, and development of T cells. It can also induce proliferation in peripheral monocytes, enhance T cell apoptosis induced by TCR/CD3 triggered activation, and regulate CD28 co-stimulation to promote Th1 cell responses. The expression of this receptor is induced by lymphocyte activation. TRAF adaptor proteins have been shown to bind to this receptor and transduce the signals leading to activation of NF-kappaB. [provided by RefSeq, Jul 2008]","start":7915894,"end":7943165,"strand":-1,"description":"TNF receptor superfamily member 9 [Source:HGNC Symbol;Acc:HGNC:11924]"}, {"versioned_ensembl_gene_id":"ENSG00000117602.11","gene_symbol":"RCAN3","gene_name":"RCAN family member 3 [Source:HGNC Symbol;Acc:HGNC:3042]","synonyms":"DSCR1L2","biotype":"protein_coding","ncbi_id":"11123","summary":null,"start":24502351,"end":24541040,"strand":1,"description":"RCAN family member 3 [Source:HGNC Symbol;Acc:HGNC:3042]"}, {"versioned_ensembl_gene_id":"ENSG00000131152.4","gene_symbol":"AC010531.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":87302876,"end":87334273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237159.5","gene_symbol":"CNTFR-AS1","gene_name":"CNTFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48712]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"415056","summary":null,"start":34568015,"end":34582829,"strand":1,"description":"CNTFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48712]"}, {"versioned_ensembl_gene_id":"ENSG00000019505.7","gene_symbol":"SYT13","gene_name":"synaptotagmin 13 [Source:HGNC Symbol;Acc:HGNC:14962]","synonyms":"KIAA1427","biotype":"protein_coding","ncbi_id":"57586","summary":"This gene encodes a member of the large synaptotagmin protein family. Family members have an extracellular N-terminal transmembrane domain and a cytoplasmic C terminus with two tandem C2 domains (C2A and C2B). Synaptotogmin family members can form homo- and heteromeric complexes with each other. They also have different biochemical properties and developmental profiles, and patterns of tissue distribution. Synaptotagmins function as membrane traffickers in multicellular organisms. Two alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":45240301,"end":45286319,"strand":-1,"description":"synaptotagmin 13 [Source:HGNC Symbol;Acc:HGNC:14962]"}, {"versioned_ensembl_gene_id":"ENSG00000261697.5","gene_symbol":"AC010531.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87262759,"end":87292438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173040.12","gene_symbol":"EVC2","gene_name":"EvC ciliary complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:19747]","synonyms":"LBN","biotype":"protein_coding","ncbi_id":"132884","summary":"This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":5542772,"end":5709548,"strand":-1,"description":"EvC ciliary complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:19747]"}, {"versioned_ensembl_gene_id":"ENSG00000122756.14","gene_symbol":"CNTFR","gene_name":"ciliary neurotrophic factor receptor [Source:HGNC Symbol;Acc:HGNC:2170]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1271","summary":"This gene encodes a member of the type 1 cytokine receptor family. The encoded protein is the ligand-specific component of a tripartite receptor for ciliary neurotrophic factor, which plays a critical role in neuronal cell survival, differentiation and gene expression. Binding of ciliary neurotrophic factor to the encoded protein recruits the transmembrane components of the receptor, gp130 and leukemia inhibitory factor receptor, facilitating signal transduction. Single nucleotide polymorphisms in this gene may be associated with variations in muscle strength, as well as early onset of eating disorders. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2011]","start":34551432,"end":34590140,"strand":-1,"description":"ciliary neurotrophic factor receptor [Source:HGNC Symbol;Acc:HGNC:2170]"}, {"versioned_ensembl_gene_id":"ENSG00000255494.1","gene_symbol":"LINC00681","gene_name":"long intergenic non-protein coding RNA 681 [Source:HGNC Symbol;Acc:HGNC:44423]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101409254","summary":null,"start":12794243,"end":12818291,"strand":1,"description":"long intergenic non-protein coding RNA 681 [Source:HGNC Symbol;Acc:HGNC:44423]"}, {"versioned_ensembl_gene_id":"ENSG00000270006.2","gene_symbol":"AC010531.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87317509,"end":87318043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254813.5","gene_symbol":"AC123777.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12765849,"end":12811478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229046.1","gene_symbol":"HMGN1P2","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4985]","synonyms":"HMGN1L2,HMG14P","biotype":"processed_pseudogene","ncbi_id":"54048","summary":null,"start":31706555,"end":31706864,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4985]"}, {"versioned_ensembl_gene_id":"ENSG00000261651.1","gene_symbol":"AC136285.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87215915,"end":87216452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269901.1","gene_symbol":"AC010531.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87362536,"end":87367476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277291.2","gene_symbol":"KRTAP5-5","gene_name":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]","synonyms":"KRTAP5.5,KRTAP5-11","biotype":"protein_coding","ncbi_id":"439915","summary":null,"start":1635485,"end":1636417,"strand":1,"description":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]"}, {"versioned_ensembl_gene_id":"ENSG00000261592.1","gene_symbol":"AC010531.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87396704,"end":87400295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281645.1","gene_symbol":"AP006285.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1668294,"end":1669053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231050.1","gene_symbol":"AL109917.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1891471,"end":1892658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254964.1","gene_symbol":"AP001458.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62606161,"end":62606405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149489.8","gene_symbol":"ROM1","gene_name":"retinal outer segment membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:10254]","synonyms":"TSPAN23,ROM","biotype":"protein_coding","ncbi_id":"6094","summary":"This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa. [provided by RefSeq, Jul 2008]","start":62611722,"end":62615120,"strand":1,"description":"retinal outer segment membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:10254]"}, {"versioned_ensembl_gene_id":"ENSG00000223655.1","gene_symbol":"RAB9AP3","gene_name":"RAB9A, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38107]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287577","summary":null,"start":25918323,"end":25918895,"strand":-1,"description":"RAB9A, member RAS oncogene family pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38107]"}, {"versioned_ensembl_gene_id":"ENSG00000254497.1","gene_symbol":"AC103681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45253884,"end":45254649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270330.1","gene_symbol":"AL009183.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7942372,"end":7942726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248376.2","gene_symbol":"AC112698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183418890,"end":183419805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282630.1","gene_symbol":"YWHAEP7","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49437]","synonyms":"LOC284100","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284100","summary":null,"start":37832458,"end":37888896,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49437]"}, {"versioned_ensembl_gene_id":"ENSG00000141428.16","gene_symbol":"C18orf21","gene_name":"chromosome 18 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:28802]","synonyms":"HsT3108,PNAS-131,PNAS-124","biotype":"protein_coding","ncbi_id":"83608","summary":null,"start":35972083,"end":35979286,"strand":1,"description":"chromosome 18 open reading frame 21 [Source:HGNC Symbol;Acc:HGNC:28802]"}, {"versioned_ensembl_gene_id":"ENSG00000005893.15","gene_symbol":"LAMP2","gene_name":"lysosomal associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:6501]","synonyms":"CD107b","biotype":"protein_coding","ncbi_id":"3920","summary":"The protein encoded by this gene is a member of a family of membrane glycoproteins. This glycoprotein provides selectins with carbohydrate ligands. It may play a role in tumor cell metastasis. It may also function in the protection, maintenance, and adhesion of the lysosome. Alternative splicing of this gene results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]","start":120427827,"end":120469365,"strand":-1,"description":"lysosomal associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:6501]"}, {"versioned_ensembl_gene_id":"ENSG00000266248.1","gene_symbol":"AC011474.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29489775,"end":29526948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277327.1","gene_symbol":"SPDYE20P","gene_name":"speedy/RINGO cell cycle regulator family member E20, pseudogene [Source:HGNC Symbol;Acc:HGNC:51516]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101060280","summary":null,"start":6715630,"end":6720982,"strand":-1,"description":"speedy/RINGO cell cycle regulator family member E20, pseudogene [Source:HGNC Symbol;Acc:HGNC:51516]"}, {"versioned_ensembl_gene_id":"ENSG00000187135.7","gene_symbol":"VSTM2B","gene_name":"V-set and transmembrane domain containing 2B [Source:HGNC Symbol;Acc:HGNC:33595]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342865","summary":null,"start":29526499,"end":29564479,"strand":1,"description":"V-set and transmembrane domain containing 2B [Source:HGNC Symbol;Acc:HGNC:33595]"}, {"versioned_ensembl_gene_id":"ENSG00000187953.10","gene_symbol":"PMS2CL","gene_name":"PMS2 C-terminal like pseudogene [Source:HGNC Symbol;Acc:HGNC:30061]","synonyms":"PMS2P13","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441194","summary":null,"start":6710128,"end":6753862,"strand":1,"description":"PMS2 C-terminal like pseudogene [Source:HGNC Symbol;Acc:HGNC:30061]"}, {"versioned_ensembl_gene_id":"ENSG00000250910.7","gene_symbol":"AC097467.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155173716,"end":155381694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278362.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54576966,"end":54586961,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000149499.11","gene_symbol":"EML3","gene_name":"echinoderm microtubule associated protein like 3 [Source:HGNC Symbol;Acc:HGNC:26666]","synonyms":"FLJ35827,ELP95","biotype":"protein_coding","ncbi_id":"256364","summary":null,"start":62602218,"end":62612765,"strand":-1,"description":"echinoderm microtubule associated protein like 3 [Source:HGNC Symbol;Acc:HGNC:26666]"}, {"versioned_ensembl_gene_id":"ENSG00000279387.1","gene_symbol":"AC011474.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29506966,"end":29509041,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157014.10","gene_symbol":"TATDN2","gene_name":"TatD DNase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28988]","synonyms":"KIAA0218","biotype":"protein_coding","ncbi_id":"9797","summary":null,"start":10248023,"end":10281218,"strand":1,"description":"TatD DNase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28988]"}, {"versioned_ensembl_gene_id":"ENSG00000267574.1","gene_symbol":"AC011474.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29448038,"end":29448380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214706.10","gene_symbol":"IFRD2","gene_name":"interferon related developmental regulator 2 [Source:HGNC Symbol;Acc:HGNC:5457]","synonyms":"SM15,SKMc15,IFNRP","biotype":"protein_coding","ncbi_id":"7866","summary":null,"start":50287732,"end":50292918,"strand":-1,"description":"interferon related developmental regulator 2 [Source:HGNC Symbol;Acc:HGNC:5457]"}, {"versioned_ensembl_gene_id":"ENSG00000168453.14","gene_symbol":"HR","gene_name":"HR, lysine demethylase and nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:5172]","synonyms":"AU,ALUNC","biotype":"protein_coding","ncbi_id":"55806","summary":"This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":22114415,"end":22133384,"strand":-1,"description":"HR, lysine demethylase and nuclear receptor corepressor [Source:HGNC Symbol;Acc:HGNC:5172]"}, {"versioned_ensembl_gene_id":"ENSG00000206353.11","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"SKIV2,DDX13,SKI2W,170A,SKIV2L1,HLP","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31949457,"end":31960128,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000124659.6","gene_symbol":"TBCC","gene_name":"tubulin folding cofactor C [Source:HGNC Symbol;Acc:HGNC:11580]","synonyms":"CFC","biotype":"protein_coding","ncbi_id":"6903","summary":"Cofactor C is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. [provided by RefSeq, Jul 2008]","start":42744481,"end":42746096,"strand":-1,"description":"tubulin folding cofactor C [Source:HGNC Symbol;Acc:HGNC:11580]"}, {"versioned_ensembl_gene_id":"ENSG00000153157.12","gene_symbol":"SYCP2L","gene_name":"synaptonemal complex protein 2 like [Source:HGNC Symbol;Acc:HGNC:21537]","synonyms":"NO145,dJ62D2.1,C6orf177","biotype":"protein_coding","ncbi_id":"221711","summary":null,"start":10886831,"end":10979320,"strand":1,"description":"synaptonemal complex protein 2 like [Source:HGNC Symbol;Acc:HGNC:21537]"}, {"versioned_ensembl_gene_id":"ENSG00000169885.9","gene_symbol":"CALML6","gene_name":"calmodulin like 6 [Source:HGNC Symbol;Acc:HGNC:24193]","synonyms":"CAGLP","biotype":"protein_coding","ncbi_id":"163688","summary":null,"start":1914827,"end":1917296,"strand":1,"description":"calmodulin like 6 [Source:HGNC Symbol;Acc:HGNC:24193]"}, {"versioned_ensembl_gene_id":"ENSG00000047056.14","gene_symbol":"WDR37","gene_name":"WD repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:31406]","synonyms":"KIAA0982","biotype":"protein_coding","ncbi_id":"22884","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]","start":1049538,"end":1132297,"strand":1,"description":"WD repeat domain 37 [Source:HGNC Symbol;Acc:HGNC:31406]"}, {"versioned_ensembl_gene_id":"ENSG00000248686.1","gene_symbol":"LINC02491","gene_name":"long intergenic non-protein coding RNA 2491 [Source:HGNC Symbol;Acc:HGNC:53475]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377467","summary":null,"start":145599109,"end":145600552,"strand":1,"description":"long intergenic non-protein coding RNA 2491 [Source:HGNC Symbol;Acc:HGNC:53475]"}, {"versioned_ensembl_gene_id":"ENSG00000281953.1","gene_symbol":"AF067845.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1368648,"end":1369833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250205.1","gene_symbol":"YWHAEP4","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49440]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481785","summary":null,"start":155381042,"end":155381239,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49440]"}, {"versioned_ensembl_gene_id":"ENSG00000281997.1","gene_symbol":"AC131901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1373685,"end":1381062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282141.1","gene_symbol":"AC131901.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1377533,"end":1379973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185149.5","gene_symbol":"NPY2R","gene_name":"neuropeptide Y receptor Y2 [Source:HGNC Symbol;Acc:HGNC:7957]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4887","summary":null,"start":155208629,"end":155217078,"strand":1,"description":"neuropeptide Y receptor Y2 [Source:HGNC Symbol;Acc:HGNC:7957]"}, {"versioned_ensembl_gene_id":"ENSG00000080910.11","gene_symbol":"CFHR2","gene_name":"complement factor H related 2 [Source:HGNC Symbol;Acc:HGNC:4890]","synonyms":"HFL3,FHR2,CFHL2","biotype":"protein_coding","ncbi_id":"3080","summary":"This gene belongs to a family of complement factor H-related genes (CFHR), which are clustered together with complement factor H gene on chromosome 1, and are involved in regulation of complement. Mutations in CFHR genes have been associated with dense deposit disease and atypical haemolytic-uraemic syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]","start":196943772,"end":196959226,"strand":1,"description":"complement factor H related 2 [Source:HGNC Symbol;Acc:HGNC:4890]"}, {"versioned_ensembl_gene_id":"ENSG00000280841.1","gene_symbol":"AC026748.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1383159,"end":1386409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229727.6","gene_symbol":"AC013460.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7421261,"end":7450254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101464.10","gene_symbol":"PIGU","gene_name":"phosphatidylinositol glycan anchor biosynthesis class U [Source:HGNC Symbol;Acc:HGNC:15791]","synonyms":"GAB1,CDC91L1,bA346K17.2","biotype":"protein_coding","ncbi_id":"128869","summary":"The protein encoded by this gene shares similarity with Saccharomyces cerevisiae Cdc91, a predicted integral membrane protein that may function in cell division control. The protein encoded by this gene is the fifth subunit of GPI transamidase that attaches GPI-anchors to proteins. [provided by RefSeq, Jul 2008]","start":34560542,"end":34698790,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class U [Source:HGNC Symbol;Acc:HGNC:15791]"}, {"versioned_ensembl_gene_id":"ENSG00000112624.12","gene_symbol":"BICRAL","gene_name":"BRD4 interacting chromatin remodeling complex associated protein like [Source:HGNC Symbol;Acc:HGNC:21111]","synonyms":"KIAA0240,GLTSCR1L","biotype":"protein_coding","ncbi_id":"23506","summary":null,"start":42746958,"end":42868560,"strand":1,"description":"BRD4 interacting chromatin remodeling complex associated protein like [Source:HGNC Symbol;Acc:HGNC:21111]"}, {"versioned_ensembl_gene_id":"ENSG00000264443.1","gene_symbol":"AL445686.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24538802,"end":24556024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139168.7","gene_symbol":"ZCRB1","gene_name":"zinc finger CCHC-type and RNA binding motif containing 1 [Source:HGNC Symbol;Acc:HGNC:29620]","synonyms":"ZCCHC19,SNRNP31,RBM36,MADP1,MADP-1","biotype":"protein_coding","ncbi_id":"85437","summary":"Pre-mRNA splicing is catalyzed by the spliceosome. U12-type spliceosome binds U12-type pre-mRNAs and recognizes the 5' splice site and branch-point sequence. U11 and U12 snRNPs are components of U12-type spliceosome and function as a molecular bridge connecting both ends of the intron. The protein encoded by this gene contains a RNA recognition motif. It was identified as one of the protein components of U11/U12 snRNPs. This protein and many other U11/U12 snRNP proteins are highly conserved in organisms known to contain U12-type introns. These proteins have been shown to be essential for cell viability, suggesting the key roles in U12-type splicing. [provided by RefSeq, Jul 2008]","start":42312078,"end":42326118,"strand":-1,"description":"zinc finger CCHC-type and RNA binding motif containing 1 [Source:HGNC Symbol;Acc:HGNC:29620]"}, {"versioned_ensembl_gene_id":"ENSG00000164114.18","gene_symbol":"MAP9","gene_name":"microtubule associated protein 9 [Source:HGNC Symbol;Acc:HGNC:26118]","synonyms":"FLJ21159,ASAP","biotype":"protein_coding","ncbi_id":"79884","summary":"ASAP is a microtubule-associated protein required for spindle function, mitotic progression, and cytokinesis (Saffin et al., 2005 [PubMed 16049101]).[supplied by OMIM, Mar 2008]","start":155342658,"end":155376970,"strand":-1,"description":"microtubule associated protein 9 [Source:HGNC Symbol;Acc:HGNC:26118]"}, {"versioned_ensembl_gene_id":"ENSG00000157020.17","gene_symbol":"SEC13","gene_name":"SEC13 homolog, nuclear pore and COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10697]","synonyms":"SEC13R,SEC13L1,npp-20,D3S1231E","biotype":"protein_coding","ncbi_id":"6396","summary":"The protein encoded by this gene belongs to the SEC13 family of WD-repeat proteins. It is a constituent of the endoplasmic reticulum and the nuclear pore complex. It has similarity to the yeast SEC13 protein, which is required for vesicle biogenesis from endoplasmic reticulum during the transport of proteins. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Oct 2008]","start":10293131,"end":10321178,"strand":-1,"description":"SEC13 homolog, nuclear pore and COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10697]"}, {"versioned_ensembl_gene_id":"ENSG00000076242.14","gene_symbol":"MLH1","gene_name":"mutL homolog 1 [Source:HGNC Symbol;Acc:HGNC:7127]","synonyms":"HNPCC,FCC2,COCA2,HNPCC2","biotype":"protein_coding","ncbi_id":"4292","summary":"The protein encoded by this gene can heterodimerize with mismatch repair endonuclease PMS2 to form MutL alpha, part of the DNA mismatch repair system. When MutL alpha is bound by MutS beta and some accessory proteins, the PMS2 subunit of MutL alpha introduces a single-strand break near DNA mismatches, providing an entry point for exonuclease degradation. The encoded protein is also involved in DNA damage signaling and can heterodimerize with DNA mismatch repair protein MLH3 to form MutL gamma, which is involved in meiosis. This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). [provided by RefSeq, Aug 2017]","start":36993332,"end":37050918,"strand":1,"description":"mutL homolog 1 [Source:HGNC Symbol;Acc:HGNC:7127]"}, {"versioned_ensembl_gene_id":"ENSG00000278986.1","gene_symbol":"AC091060.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35972151,"end":35973916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244414.6","gene_symbol":"CFHR1","gene_name":"complement factor H related 1 [Source:HGNC Symbol;Acc:HGNC:4888]","synonyms":"CFHL1,CFHL,HFL2,HFL1,H36-2,H36-1,FHR1,CFHR1P,CFHL1P","biotype":"protein_coding","ncbi_id":"3078","summary":"This gene encodes a secreted protein belonging to the complement factor H protein family. It binds to Pseudomonas aeruginosa elongation factor Tuf together with plasminogen, which is proteolytically activated. It is proposed that Tuf acts as a virulence factor by acquiring host proteins to the pathogen surface, controlling complement, and facilitating tissue invasion. Mutations in this gene are associated with an increased risk of atypical hemolytic-uremic syndrome. [provided by RefSeq, Oct 2009]","start":196819757,"end":196832189,"strand":1,"description":"complement factor H related 1 [Source:HGNC Symbol;Acc:HGNC:4888]"}, {"versioned_ensembl_gene_id":"ENSG00000225098.1","gene_symbol":"BCRP1","gene_name":"breakpoint cluster region pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39073]","synonyms":"BCR-1","biotype":"unprocessed_pseudogene","ncbi_id":"644079","summary":null,"start":24259929,"end":24263764,"strand":-1,"description":"breakpoint cluster region pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39073]"}, {"versioned_ensembl_gene_id":"ENSG00000168386.18","gene_symbol":"FILIP1L","gene_name":"filamin A interacting protein 1 like [Source:HGNC Symbol;Acc:HGNC:24589]","synonyms":"GIP130,DOC-1","biotype":"protein_coding","ncbi_id":"11259","summary":null,"start":99830141,"end":100114513,"strand":-1,"description":"filamin A interacting protein 1 like [Source:HGNC Symbol;Acc:HGNC:24589]"}, {"versioned_ensembl_gene_id":"ENSG00000281736.1","gene_symbol":"LINC01511","gene_name":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]","synonyms":"RP11-325I22.2","biotype":"lincRNA","ncbi_id":"100506791","summary":null,"start":1363582,"end":1380067,"strand":-1,"description":"long intergenic non-protein coding RNA 1511 [Source:HGNC Symbol;Acc:HGNC:51200]"}, {"versioned_ensembl_gene_id":"ENSG00000128262.8","gene_symbol":"POM121L9P","gene_name":"POM121 transmembrane nucleoporin like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:30080]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"29774","summary":"This locus is inferred to be a transcribed pseudogene based on the observation that protein homology is limited to the first of seven exons (indicated by alignment of AL117401.1 to the assembled human genome). This pattern suggests rapid turnover by the nonsense-mediated decay pathway. [provided by RefSeq, Jul 2008]","start":24251828,"end":24265525,"strand":1,"description":"POM121 transmembrane nucleoporin like 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:30080]"}, {"versioned_ensembl_gene_id":"ENSG00000272689.1","gene_symbol":"AC004832.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30421206,"end":30421536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281511.1","gene_symbol":"MTCO2P32","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52161]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075196","summary":null,"start":1370543,"end":1370945,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52161]"}, {"versioned_ensembl_gene_id":"ENSG00000104368.17","gene_symbol":"PLAT","gene_name":"plasminogen activator, tissue type [Source:HGNC Symbol;Acc:HGNC:9051]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5327","summary":"This gene encodes tissue-type plasminogen activator, a secreted serine protease that converts the proenzyme plasminogen to plasmin, a fibrinolytic enzyme. The encoded preproprotein is proteolytically processed by plasmin or trypsin to generate heavy and light chains. These chains associate via disulfide linkages to form the heterodimeric enzyme. This enzyme plays a role in cell migration and tissue remodeling. Increased enzymatic activity causes hyperfibrinolysis, which manifests as excessive bleeding, while decreased activity leads to hypofibrinolysis, which can result in thrombosis or embolism. Alternative splicing of this gene results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":42175233,"end":42207724,"strand":-1,"description":"plasminogen activator, tissue type [Source:HGNC Symbol;Acc:HGNC:9051]"}, {"versioned_ensembl_gene_id":"ENSG00000233179.1","gene_symbol":"Z82249.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48448890,"end":48451217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282152.1","gene_symbol":"DLGAP2","gene_name":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]","synonyms":"ERICH1-AS1,ERICH1-AS1,DAP2,DAP-2,C8orf68,SAPAP2,C8orf68","biotype":"protein_coding","ncbi_id":"9228","summary":"The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]","start":1487682,"end":1552210,"strand":1,"description":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]"}, {"versioned_ensembl_gene_id":"ENSG00000275457.1","gene_symbol":"AL117332.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21302731,"end":21303704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205111.8","gene_symbol":"CDKL4","gene_name":"cyclin dependent kinase like 4 [Source:HGNC Symbol;Acc:HGNC:19287]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344387","summary":null,"start":39175646,"end":39229588,"strand":-1,"description":"cyclin dependent kinase like 4 [Source:HGNC Symbol;Acc:HGNC:19287]"}, {"versioned_ensembl_gene_id":"ENSG00000088930.7","gene_symbol":"XRN2","gene_name":"5'-3' exoribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:12836]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22803","summary":"This gene encodes a 5'-3' exonuclease that promotes transcription termination at cotranscriptional cleavage sites. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":21303304,"end":21389827,"strand":1,"description":"5'-3' exoribonuclease 2 [Source:HGNC Symbol;Acc:HGNC:12836]"}, {"versioned_ensembl_gene_id":"ENSG00000198646.13","gene_symbol":"NCOA6","gene_name":"nuclear receptor coactivator 6 [Source:HGNC Symbol;Acc:HGNC:15936]","synonyms":"TRBP,RAP250,PRIP,NRC,KIAA0181,ASC2,AIB3","biotype":"protein_coding","ncbi_id":"23054","summary":"The protein encoded by this gene is a transcriptional coactivator that can interact with nuclear hormone receptors to enhance their transcriptional activator functions. This protein has been shown to be involved in the hormone-dependent coactivation of several receptors, including prostanoid, retinoid, vitamin D3, thyroid hormone, and steroid receptors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2011]","start":34689097,"end":34825649,"strand":-1,"description":"nuclear receptor coactivator 6 [Source:HGNC Symbol;Acc:HGNC:15936]"}, {"versioned_ensembl_gene_id":"ENSG00000282001.1","gene_symbol":"DLGAP2-AS1","gene_name":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507435","summary":null,"start":1551825,"end":1552054,"strand":-1,"description":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]"}, {"versioned_ensembl_gene_id":"ENSG00000147224.10","gene_symbol":"PRPS1","gene_name":"phosphoribosyl pyrophosphate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:9462]","synonyms":"DFN2,CMTX5,DFNX1","biotype":"protein_coding","ncbi_id":"5631","summary":"This gene encodes an enzyme that catalyzes the phosphoribosylation of ribose 5-phosphate to 5-phosphoribosyl-1-pyrophosphate, which is necessary for purine metabolism and nucleotide biosynthesis. Defects in this gene are a cause of phosphoribosylpyrophosphate synthetase superactivity, Charcot-Marie-Tooth disease X-linked recessive type 5 and Arts Syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":107628424,"end":107651026,"strand":1,"description":"phosphoribosyl pyrophosphate synthetase 1 [Source:HGNC Symbol;Acc:HGNC:9462]"}, {"versioned_ensembl_gene_id":"ENSG00000272162.1","gene_symbol":"AL024498.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10747794,"end":10930423,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248356.1","gene_symbol":"AC093864.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145642336,"end":145650624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124479.8","gene_symbol":"NDP","gene_name":"NDP, norrin cystine knot growth factor [Source:HGNC Symbol;Acc:HGNC:7678]","synonyms":"norrin,EVR2","biotype":"protein_coding","ncbi_id":"4693","summary":"This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy. [provided by RefSeq, Feb 2009]","start":43948776,"end":43973504,"strand":-1,"description":"NDP, norrin cystine knot growth factor [Source:HGNC Symbol;Acc:HGNC:7678]"}, {"versioned_ensembl_gene_id":"ENSG00000230663.1","gene_symbol":"FAM224B","gene_name":"family with sequence similarity 224 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37737]","synonyms":"NCRNA00230B,LINC00230B","biotype":"lincRNA","ncbi_id":"401629","summary":"This locus is transcribed but does not appear to encode a protein. Two identical copies of this gene are present in a palindromic region on chromosome Y. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":17552800,"end":17579754,"strand":-1,"description":"family with sequence similarity 224 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37737]"}, {"versioned_ensembl_gene_id":"ENSG00000151611.13","gene_symbol":"MMAA","gene_name":"methylmalonic aciduria (cobalamin deficiency) cblA type [Source:HGNC Symbol;Acc:HGNC:18871]","synonyms":"cblA","biotype":"protein_coding","ncbi_id":"166785","summary":"The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008]","start":145618263,"end":145660035,"strand":1,"description":"methylmalonic aciduria (cobalamin deficiency) cblA type [Source:HGNC Symbol;Acc:HGNC:18871]"}, {"versioned_ensembl_gene_id":"ENSG00000238191.3","gene_symbol":"CLUHP1","gene_name":"clustered mitochondria homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38416]","synonyms":"KIAA0664L1,KIAA0664P1","biotype":"unprocessed_pseudogene","ncbi_id":"100418708","summary":null,"start":17621259,"end":17625832,"strand":-1,"description":"clustered mitochondria homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38416]"}, {"versioned_ensembl_gene_id":"ENSG00000280830.1","gene_symbol":"ADI1","gene_name":"acireductone dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:30576]","synonyms":"HMFT1638,FLJ10913,ARD,APL1,SIPL,mtnD,MTCBP-1","biotype":"protein_coding","ncbi_id":"55256","summary":"This gene encodes an enzyme that belongs to the aci-reductone dioxygenase family of metal-binding enzymes, which are involved in methionine salvage. This enzyme may regulate mRNA processing in the nucleus, and may carry out different functions depending on its localization. Related pseudogenes have been defined on chromosomes 8 and 20. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":3498728,"end":3502360,"strand":-1,"description":"acireductone dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:30576]"}, {"versioned_ensembl_gene_id":"ENSG00000137210.13","gene_symbol":"TMEM14B","gene_name":"transmembrane protein 14B [Source:HGNC Symbol;Acc:HGNC:21384]","synonyms":"MGC1223","biotype":"protein_coding","ncbi_id":"81853","summary":null,"start":10747759,"end":10852753,"strand":1,"description":"transmembrane protein 14B [Source:HGNC Symbol;Acc:HGNC:21384]"}, {"versioned_ensembl_gene_id":"ENSG00000281723.1","gene_symbol":"AC114810.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3498320,"end":3498795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230515.1","gene_symbol":"AC092580.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7671604,"end":7672246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236276.1","gene_symbol":"NDP-AS1","gene_name":"NDP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40395]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873919","summary":null,"start":43949732,"end":43969620,"strand":1,"description":"NDP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40395]"}, {"versioned_ensembl_gene_id":"ENSG00000243496.6","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32790888,"end":32795173,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000235576.1","gene_symbol":"LINC01871","gene_name":"long intergenic non-protein coding RNA 1871 [Source:HGNC Symbol;Acc:HGNC:52690]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929531","summary":null,"start":7725801,"end":7730705,"strand":1,"description":"long intergenic non-protein coding RNA 1871 [Source:HGNC Symbol;Acc:HGNC:52690]"}, {"versioned_ensembl_gene_id":"ENSG00000275578.1","gene_symbol":"AC007742.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17705968,"end":17708185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134365.12","gene_symbol":"CFHR4","gene_name":"complement factor H related 4 [Source:HGNC Symbol;Acc:HGNC:16979]","synonyms":"FHR4,FHR-4,CFHL4","biotype":"protein_coding","ncbi_id":"10877","summary":"This gene is a member of the complement factor H (CFH) gene family, and encodes one of the 5 CFH-related (CFHR) proteins. These 5 genes are closely linked to the CFH gene on chromosome 1q31-q32. The CFHRs are secreted plasma proteins synthesized primarily by the hepatocytes, and composed of highly-related short consensus repeats (SCRs). This protein enhances the cofactor activity of CFH, and is involved in complement regulation. It can associate with lipoproteins and may play a role in lipid metabolism. Alternatively spliced transcript variants encoding different isoforms (varying in the number of SCRs) have been described for this gene. [provided by RefSeq, Jan 2011]","start":196850241,"end":196918972,"strand":1,"description":"complement factor H related 4 [Source:HGNC Symbol;Acc:HGNC:16979]"}, {"versioned_ensembl_gene_id":"ENSG00000227635.1","gene_symbol":"USP9YP21","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38757]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480355","summary":null,"start":25933833,"end":25935881,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38757]"}, {"versioned_ensembl_gene_id":"ENSG00000280733.1","gene_symbol":"LINC01238","gene_name":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]","synonyms":"FLJ40615,FLJ40615","biotype":"lincRNA","ncbi_id":"102723927","summary":null,"start":241970683,"end":241977276,"strand":1,"description":"long intergenic non-protein coding RNA 1238 [Source:HGNC Symbol;Acc:HGNC:49795]"}, {"versioned_ensembl_gene_id":"ENSG00000224975.1","gene_symbol":"INE1","gene_name":"inactivation escape 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6060]","synonyms":"NCRNA00010","biotype":"sense_intronic","ncbi_id":"8552","summary":"X chromosome inactivation provides dosage compensation for the expression level of X-linked genes from the single X in males and the two in females. This X chromosome gene is intronless and was identified because its transcription escapes X inactivation in females. This gene does not make a protein.[provided by RefSeq, May 2010]","start":47204921,"end":47205865,"strand":1,"description":"inactivation escape 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6060]"}, {"versioned_ensembl_gene_id":"ENSG00000250218.1","gene_symbol":"ALDH1L1-AS1","gene_name":"ALDH1L1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40244]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874204","summary":null,"start":126103640,"end":126108069,"strand":1,"description":"ALDH1L1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40244]"}, {"versioned_ensembl_gene_id":"ENSG00000237546.1","gene_symbol":"XKRYP6","gene_name":"XK related, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23913]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379033","summary":null,"start":25943268,"end":25954152,"strand":1,"description":"XK related, Y-linked pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23913]"}, {"versioned_ensembl_gene_id":"ENSG00000232979.1","gene_symbol":"AC092580.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7735645,"end":7735783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246022.2","gene_symbol":"ALDH1L1-AS2","gene_name":"ALDH1L1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42446]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100862662","summary":null,"start":126180065,"end":126210169,"strand":1,"description":"ALDH1L1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42446]"}, {"versioned_ensembl_gene_id":"ENSG00000130985.16","gene_symbol":"UBA1","gene_name":"ubiquitin like modifier activating enzyme 1 [Source:HGNC Symbol;Acc:HGNC:12469]","synonyms":"UBE1X,UBE1,POC20,GXP1,CFAP124,A1S9T","biotype":"protein_coding","ncbi_id":"7317","summary":"The protein encoded by this gene catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. This gene complements an X-linked mouse temperature-sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11.23. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]","start":47190861,"end":47215128,"strand":1,"description":"ubiquitin like modifier activating enzyme 1 [Source:HGNC Symbol;Acc:HGNC:12469]"}, {"versioned_ensembl_gene_id":"ENSG00000232328.1","gene_symbol":"AC084030.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":236733382,"end":236754363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106355.9","gene_symbol":"LSM5","gene_name":"LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17162]","synonyms":"YER146W","biotype":"protein_coding","ncbi_id":"23658","summary":"Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]","start":32485332,"end":32495283,"strand":-1,"description":"LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:17162]"}, {"versioned_ensembl_gene_id":"ENSG00000281733.1","gene_symbol":"FAM99A","gene_name":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]","synonyms":"FLJ42833","biotype":"lincRNA","ncbi_id":"387742","summary":null,"start":1671307,"end":1673566,"strand":1,"description":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]"}, {"versioned_ensembl_gene_id":"ENSG00000172283.10","gene_symbol":"PRYP4","gene_name":"PTPN13-like, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:34021]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442866","summary":null,"start":25975549,"end":25988069,"strand":1,"description":"PTPN13-like, Y-linked pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:34021]"}, {"versioned_ensembl_gene_id":"ENSG00000282061.1","gene_symbol":"AC025674.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57251821,"end":57252305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282395.1","gene_symbol":"LINC01606","gene_name":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]","synonyms":"TCONS_l2_00027778","biotype":"lincRNA","ncbi_id":"100507651","summary":null,"start":57193590,"end":57252058,"strand":1,"description":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]"}, {"versioned_ensembl_gene_id":"ENSG00000253976.1","gene_symbol":"AC022679.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55135203,"end":55142358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248522.1","gene_symbol":"SBF1P1","gene_name":"SET binding factor 1 pseudogene 1 [Source:NCBI gene;Acc:100133234]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133234","summary":null,"start":55449509,"end":55455139,"strand":-1,"description":"SET binding factor 1 pseudogene 1 [Source:NCBI gene;Acc:100133234]"}, {"versioned_ensembl_gene_id":"ENSG00000230427.1","gene_symbol":"AC095033.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95061596,"end":95067545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227867.1","gene_symbol":"ELOCP11","gene_name":"elongin C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:38147]","synonyms":"TCEB1P11","biotype":"processed_pseudogene","ncbi_id":"100462872","summary":null,"start":25991241,"end":25991572,"strand":-1,"description":"elongin C pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:38147]"}, {"versioned_ensembl_gene_id":"ENSG00000206579.8","gene_symbol":"XKR4","gene_name":"XK related 4 [Source:HGNC Symbol;Acc:HGNC:29394]","synonyms":"KIAA1889","biotype":"protein_coding","ncbi_id":"114786","summary":null,"start":55102389,"end":55542054,"strand":1,"description":"XK related 4 [Source:HGNC Symbol;Acc:HGNC:29394]"}, {"versioned_ensembl_gene_id":"ENSG00000184811.3","gene_symbol":"TUSC5","gene_name":"tumor suppressor candidate 5 [Source:HGNC Symbol;Acc:HGNC:29592]","synonyms":"LOST1,IFITMD3,BEC-1","biotype":"protein_coding","ncbi_id":"286753","summary":null,"start":1279663,"end":1300987,"strand":1,"description":"tumor suppressor candidate 5 [Source:HGNC Symbol;Acc:HGNC:29592]"}, {"versioned_ensembl_gene_id":"ENSG00000262686.1","gene_symbol":"GLIS2-AS1","gene_name":"GLIS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51381]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926896","summary":null,"start":4324667,"end":4328340,"strand":-1,"description":"GLIS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51381]"}, {"versioned_ensembl_gene_id":"ENSG00000254198.1","gene_symbol":"AC113191.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43125995,"end":43126397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172339.9","gene_symbol":"ALG14","gene_name":"ALG14, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:28287]","synonyms":"MGC19780","biotype":"protein_coding","ncbi_id":"199857","summary":"This gene is a member of the glycosyltransferase 1 family. The encoded protein and ALG13 are thought to be subunits of UDP-GlcNAc transferase, which catalyzes the first two committed steps in endoplasmic reticulum N-linked glycosylation. Mutations in this gene have been linked to congenital myasthenic syndrome (CMSWTA). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]","start":94974407,"end":95072945,"strand":-1,"description":"ALG14, UDP-N-acetylglucosaminyltransferase subunit [Source:HGNC Symbol;Acc:HGNC:28287]"}, {"versioned_ensembl_gene_id":"ENSG00000135862.5","gene_symbol":"LAMC1","gene_name":"laminin subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:6492]","synonyms":"LAMB2","biotype":"protein_coding","ncbi_id":"3915","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins, composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively), have a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the gamma chain isoform laminin, gamma 1. The gamma 1 chain, formerly thought to be a beta chain, contains structural domains similar to beta chains, however, lacks the short alpha region separating domains I and II. The structural organization of this gene also suggested that it had diverged considerably from the beta chain genes. Embryos of transgenic mice in which both alleles of the gamma 1 chain gene were inactivated by homologous recombination, lacked basement membranes, indicating that laminin, gamma 1 chain is necessary for laminin heterotrimer assembly. It has been inferred by analogy with the strikingly similar 3' UTR sequence in mouse laminin gamma 1 cDNA, that multiple polyadenylation sites are utilized in human to generate the 2 different sized mRNAs (5.5 and 7.5 kb) seen on Northern analysis. [provided by RefSeq, Aug 2011]","start":183023460,"end":183145592,"strand":1,"description":"laminin subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:6492]"}, {"versioned_ensembl_gene_id":"ENSG00000257564.1","gene_symbol":"AC068993.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78793526,"end":78794114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243477.5","gene_symbol":"NAT6","gene_name":"N-acetyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:30252]","synonyms":"FUS2","biotype":"protein_coding","ncbi_id":"24142","summary":"This gene encodes a member of the N-acetyltransferase family. N-acetyltransferases modify proteins by transferring acetyl groups from acetyl CoA to the N-termini of protein substrates. The encoded protein is a cytoplasmic N-acetyltransferase with a substrate specificity for proteins with an N-terminal methionine. This gene is located in the tumor suppressor gene region on chromosome 3p21.3 and the encoded protein may play a role in cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed. This gene overlaps and is on the same strand as hyaluronoglucosaminidase 3, and some transcripts of each gene share a portion of the first exon. [provided by RefSeq, Jan 2011]","start":50296402,"end":50299421,"strand":-1,"description":"N-acetyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:30252]"}, {"versioned_ensembl_gene_id":"ENSG00000249245.2","gene_symbol":"NCOA4P3","gene_name":"nuclear receptor coactivator 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729497","summary":null,"start":145624159,"end":145626035,"strand":-1,"description":"nuclear receptor coactivator 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52404]"}, {"versioned_ensembl_gene_id":"ENSG00000257948.1","gene_symbol":"AC068993.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78804348,"end":78808499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254302.1","gene_symbol":"AC087855.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34174886,"end":34184895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253108.1","gene_symbol":"AC090993.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34228439,"end":34346731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251468.2","gene_symbol":"AC135352.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12958387,"end":12962200,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254033.1","gene_symbol":"AC087855.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34229294,"end":34248946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254357.1","gene_symbol":"AC090200.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55517240,"end":55520977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250305.8","gene_symbol":"KIAA1456","gene_name":"KIAA1456 [Source:HGNC Symbol;Acc:HGNC:26725]","synonyms":"TRM9L,FLJ36980,C8orf79","biotype":"protein_coding","ncbi_id":"57604","summary":null,"start":12945642,"end":13031503,"strand":1,"description":"KIAA1456 [Source:HGNC Symbol;Acc:HGNC:26725]"}, {"versioned_ensembl_gene_id":"ENSG00000215264.4","gene_symbol":"RPL10AP3","gene_name":"ribosomal protein L10a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29803]","synonyms":"HsT23218","biotype":"processed_pseudogene","ncbi_id":"137107","summary":null,"start":34322992,"end":34323642,"strand":-1,"description":"ribosomal protein L10a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29803]"}, {"versioned_ensembl_gene_id":"ENSG00000253857.1","gene_symbol":"AC022679.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55161483,"end":55164727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186086.18","gene_symbol":"NBPF6","gene_name":"NBPF member 6 [Source:HGNC Symbol;Acc:HGNC:31988]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653149","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2013]","start":108450282,"end":108471002,"strand":1,"description":"NBPF member 6 [Source:HGNC Symbol;Acc:HGNC:31988]"}, {"versioned_ensembl_gene_id":"ENSG00000226449.1","gene_symbol":"CDY5P","gene_name":"chromodomain Y-linked 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:23850]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378008","summary":null,"start":17721598,"end":17723177,"strand":1,"description":"chromodomain Y-linked 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:23850]"}, {"versioned_ensembl_gene_id":"ENSG00000237495.9","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31752963,"end":31760319,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000229405.1","gene_symbol":"AC092580.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7736438,"end":7737095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276911.1","gene_symbol":"BX248415.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":196819745,"end":196959210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280591.1","gene_symbol":"AC237191.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242003691,"end":242006013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243449.6","gene_symbol":"C4orf48","gene_name":"chromosome 4 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:34437]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401115","summary":null,"start":2041993,"end":2043970,"strand":1,"description":"chromosome 4 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:34437]"}, {"versioned_ensembl_gene_id":"ENSG00000225896.1","gene_symbol":"AC007742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17726752,"end":17727080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280691.1","gene_symbol":"AC237191.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242030558,"end":242031529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280980.1","gene_symbol":"AC093642.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":242053059,"end":242089513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236914.3","gene_symbol":"LINC01852","gene_name":"long intergenic non-protein coding RNA 1852 [Source:HGNC Symbol;Acc:HGNC:52668]","synonyms":"ENST00000434223","biotype":"lincRNA","ncbi_id":"107984773","summary":null,"start":38069481,"end":38072959,"strand":-1,"description":"long intergenic non-protein coding RNA 1852 [Source:HGNC Symbol;Acc:HGNC:52668]"}, {"versioned_ensembl_gene_id":"ENSG00000186792.16","gene_symbol":"HYAL3","gene_name":"hyaluronoglucosaminidase 3 [Source:HGNC Symbol;Acc:HGNC:5322]","synonyms":"Minna14,LUCA14,LUCA-3","biotype":"protein_coding","ncbi_id":"8372","summary":"This gene encodes a member of the hyaluronidase family. Hyaluronidases are endoglycosidase enzymes that degrade hyaluronan, one of the major glycosaminoglycans of the extracellular matrix. The regulated turnover of hyaluronan plays a critical role in many biological processes including cell proliferation, migration and differentiation. The encoded protein may also play an important role in sperm function. This gene is one of several related genes in a region of chromosome 3p21.3 associated with tumor suppression, and the expression of specific transcript variants may be indicative of tumor status. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and some isoforms may lack hyaluronidase activity. This gene overlaps and is on the same strand as N-acetyltransferase 6 (GCN5-related), and some transcripts of each gene share a portion of the first exon. [provided by RefSeq, Jan 2011]","start":50292831,"end":50299468,"strand":-1,"description":"hyaluronoglucosaminidase 3 [Source:HGNC Symbol;Acc:HGNC:5322]"}, {"versioned_ensembl_gene_id":"ENSG00000206073.10","gene_symbol":"SERPINB4","gene_name":"serpin family B member 4 [Source:HGNC Symbol;Acc:HGNC:10570]","synonyms":"SCCA2,SCCA1,SCCA-2,PI11,LEUPIN","biotype":"protein_coding","ncbi_id":"6318","summary":"The protein encoded by this gene is a member of the serpin family of serine protease inhibitors. The encoded protein is highly expressed in many tumor cells and can inactivate granzyme M, an enzyme that kills tumor cells. This protein, along with serpin B3, can be processed into smaller fragments that aggregate to form an autoantigen in psoriasis, probably by causing chronic inflammation. [provided by RefSeq, Jan 2017]","start":63637259,"end":63644298,"strand":-1,"description":"serpin family B member 4 [Source:HGNC Symbol;Acc:HGNC:10570]"}, {"versioned_ensembl_gene_id":"ENSG00000224166.1","gene_symbol":"PRYP1","gene_name":"PTPN13-like, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34018]","synonyms":"PRYP7,PRY4P","biotype":"unprocessed_pseudogene","ncbi_id":"442863","summary":null,"start":17729528,"end":17744596,"strand":-1,"description":"PTPN13-like, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34018]"}, {"versioned_ensembl_gene_id":"ENSG00000281782.1","gene_symbol":"AC093642.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":242100269,"end":242121607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226506.5","gene_symbol":"AC007463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7886770,"end":7899655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146776.14","gene_symbol":"ATXN7L1","gene_name":"ataxin 7 like 1 [Source:HGNC Symbol;Acc:HGNC:22210]","synonyms":"MGC33190,KIAA1218,ATXN7L4","biotype":"protein_coding","ncbi_id":"222255","summary":null,"start":105605067,"end":105876604,"strand":-1,"description":"ataxin 7 like 1 [Source:HGNC Symbol;Acc:HGNC:22210]"}, {"versioned_ensembl_gene_id":"ENSG00000229129.1","gene_symbol":"ACTG1P2","gene_name":"actin gamma 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:147]","synonyms":"ACTL2,ACTGP2","biotype":"processed_pseudogene","ncbi_id":"74","summary":null,"start":17757001,"end":17758125,"strand":-1,"description":"actin gamma 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:147]"}, {"versioned_ensembl_gene_id":"ENSG00000249924.2","gene_symbol":"AC097467.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155286162,"end":155287136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250538.5","gene_symbol":"AC104407.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155206529,"end":155209027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000014919.12","gene_symbol":"COX15","gene_name":"COX15, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:2263]","synonyms":"CEMCOX2","biotype":"protein_coding","ncbi_id":"1355","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be essential for the biogenesis of COX formation and may function in the hydroxylation of heme O, according to the yeast mutant studies. This protein is predicted to contain 5 transmembrane domains localized in the mitochondrial inner membrane. Alternative splicing of this gene generates two transcript variants diverging in the 3' region. [provided by RefSeq, Jul 2008]","start":99711844,"end":99732100,"strand":-1,"description":"COX15, cytochrome c oxidase assembly homolog [Source:HGNC Symbol;Acc:HGNC:2263]"}, {"versioned_ensembl_gene_id":"ENSG00000259658.5","gene_symbol":"AC027559.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101732201,"end":101746870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224468.3","gene_symbol":"AL354953.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":183138402,"end":183141282,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282386.1","gene_symbol":"AL358472.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153964361,"end":153965070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145283.7","gene_symbol":"SLC10A6","gene_name":"solute carrier family 10 member 6 [Source:HGNC Symbol;Acc:HGNC:30603]","synonyms":"SOAT","biotype":"protein_coding","ncbi_id":"345274","summary":null,"start":86823468,"end":86849263,"strand":-1,"description":"solute carrier family 10 member 6 [Source:HGNC Symbol;Acc:HGNC:30603]"}, {"versioned_ensembl_gene_id":"ENSG00000272654.1","gene_symbol":"AL358472.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153977743,"end":153979160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281732.1","gene_symbol":"Z84468.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":48538900,"end":48547387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124835.2","gene_symbol":"AC105760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":237048599,"end":237056167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170631.14","gene_symbol":"ZNF16","gene_name":"zinc finger protein 16 [Source:HGNC Symbol;Acc:HGNC:12947]","synonyms":"KOX9","biotype":"protein_coding","ncbi_id":"7564","summary":"The protein encoded by this gene contains multiple tandem zinc finger motifs. The encoded protein is involved in the differentiation of erythroid and megakaryocytic cells. This gene is located in a cluster of related genes on chromosome 8 encoding zinc finger proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012]","start":144930358,"end":144950888,"strand":-1,"description":"zinc finger protein 16 [Source:HGNC Symbol;Acc:HGNC:12947]"}, {"versioned_ensembl_gene_id":"ENSG00000273026.1","gene_symbol":"AL358472.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153966516,"end":153966930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231716.1","gene_symbol":"CDY23P","gene_name":"chromodomain Y-linked 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:23867]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386745","summary":null,"start":25994684,"end":25995697,"strand":-1,"description":"chromodomain Y-linked 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:23867]"}, {"versioned_ensembl_gene_id":"ENSG00000143543.14","gene_symbol":"JTB","gene_name":"jumping translocation breakpoint [Source:HGNC Symbol;Acc:HGNC:6201]","synonyms":"hJT,PAR","biotype":"protein_coding","ncbi_id":"10899","summary":null,"start":153974269,"end":153977688,"strand":-1,"description":"jumping translocation breakpoint [Source:HGNC Symbol;Acc:HGNC:6201]"}, {"versioned_ensembl_gene_id":"ENSG00000227042.1","gene_symbol":"AC003666.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10242339,"end":10365323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206340.10","gene_symbol":"C4A","gene_name":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]","synonyms":"C4A2,C4A6,CO4,C4,C4A4,C4S,RG,C4A3,C4B,CPAMD2","biotype":"protein_coding","ncbi_id":"720","summary":"This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain is cleaved to release C4 anaphylatoxin, an antimicrobial peptide and a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":31972402,"end":31993060,"strand":1,"description":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]"}, {"versioned_ensembl_gene_id":"ENSG00000105655.18","gene_symbol":"ISYNA1","gene_name":"inositol-3-phosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:29821]","synonyms":"IPS,INOS,Ino1","biotype":"protein_coding","ncbi_id":"51477","summary":"This gene encodes an inositol-3-phosphate synthase enzyme. The encoded protein plays a critical role in the myo-inositol biosynthesis pathway by catalyzing the rate-limiting conversion of glucose 6-phosphate to myoinositol 1-phosphate. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 4. [provided by RefSeq, Nov 2011]","start":18434388,"end":18438301,"strand":-1,"description":"inositol-3-phosphate synthase 1 [Source:HGNC Symbol;Acc:HGNC:29821]"}, {"versioned_ensembl_gene_id":"ENSG00000219438.8","gene_symbol":"FAM19A5","gene_name":"family with sequence similarity 19 member A5, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21592]","synonyms":"TAFA-5","biotype":"protein_coding","ncbi_id":"25817","summary":"This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines that act as regulators of immune and nervous cells. [provided by RefSeq, Sep 2013]","start":48489460,"end":48850912,"strand":1,"description":"family with sequence similarity 19 member A5, C-C motif chemokine like [Source:HGNC Symbol;Acc:HGNC:21592]"}, {"versioned_ensembl_gene_id":"ENSG00000253525.1","gene_symbol":"AC104966.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91157285,"end":91158748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211808.3","gene_symbol":"TRAV8-7","gene_name":"T-cell receptor alpha variable 8-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12152]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28679","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22132553,"end":22133034,"strand":1,"description":"T-cell receptor alpha variable 8-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12152]"}, {"versioned_ensembl_gene_id":"ENSG00000228700.1","gene_symbol":"AC010655.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128433422,"end":128433713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115718.17","gene_symbol":"PROC","gene_name":"protein C, inactivator of coagulation factors Va and VIIIa [Source:HGNC Symbol;Acc:HGNC:9451]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5624","summary":"This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.[provided by RefSeq, Dec 2009]","start":127418427,"end":127429246,"strand":1,"description":"protein C, inactivator of coagulation factors Va and VIIIa [Source:HGNC Symbol;Acc:HGNC:9451]"}, {"versioned_ensembl_gene_id":"ENSG00000226509.1","gene_symbol":"AC005588.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153968665,"end":153968826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229861.8","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"C6orf14,MRPS18-2,HSPC183,PTD017","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30696164,"end":30704850,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000172915.18","gene_symbol":"NBEA","gene_name":"neurobeachin [Source:HGNC Symbol;Acc:HGNC:7648]","synonyms":"LYST2,KIAA1544,FLJ10197,BCL8B","biotype":"protein_coding","ncbi_id":"26960","summary":"This gene encodes a member of a large, diverse group of A-kinase anchor proteins that target the activity of protein kinase A to specific subcellular sites by binding to its type II regulatory subunits. Brain-specific expression and coat protein-like membrane recruitment of a highly similar protein in mouse suggest an involvement in neuronal post-Golgi membrane traffic. Mutations in this gene may be associated with a form of autism. This gene and its expression are frequently disrupted in patients with multiple myeloma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants may exist, but their full-length nature has not been determined.[provided by RefSeq, Feb 2011]","start":34942287,"end":35673022,"strand":1,"description":"neurobeachin [Source:HGNC Symbol;Acc:HGNC:7648]"}, {"versioned_ensembl_gene_id":"ENSG00000147234.10","gene_symbol":"FRMPD3","gene_name":"FERM and PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29382]","synonyms":"KIAA1817,RP5-1070B1.1","biotype":"protein_coding","ncbi_id":"84443","summary":"This gene encodes a protein that contains a PDZ (post synaptic density protein (PSD95), Drosophila disc large tumor suppressor (Dlg1), and zonula occludens-1 protein (zo-1) domain at the N-terminus followed by a FERM domain. The encoded protein is involved in signal transduction. The PDZ domain is thought to function in protein-protein interactions, mainly by binding to specific C-terminal peptides of other proteins. The FERM domain is found in proteins that are localized to the plasma membrane and are associated with the cytoskeleton. [provided by RefSeq, May 2017]","start":107522450,"end":107605251,"strand":1,"description":"FERM and PDZ domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29382]"}, {"versioned_ensembl_gene_id":"ENSG00000137815.14","gene_symbol":"RTF1","gene_name":"RTF1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:28996]","synonyms":"KIAA0252","biotype":"protein_coding","ncbi_id":"23168","summary":"This locus may represent a gene involved in regulation of transcription elongation and chromatin remodeling, based on studies of similar proteins in other organisms. The encoded protein may bind single-stranded DNA. [provided by RefSeq, Sep 2010]","start":41408408,"end":41483563,"strand":1,"description":"RTF1 homolog, Paf1/RNA polymerase II complex component [Source:HGNC Symbol;Acc:HGNC:28996]"}, {"versioned_ensembl_gene_id":"ENSG00000214526.3","gene_symbol":"AP000343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23322543,"end":23322927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108091.10","gene_symbol":"CCDC6","gene_name":"coiled-coil domain containing 6 [Source:HGNC Symbol;Acc:HGNC:18782]","synonyms":"TST1,TPC,PTC,H4,D10S170","biotype":"protein_coding","ncbi_id":"8030","summary":"This gene encodes a coiled-coil domain-containing protein. The encoded protein is ubiquitously expressed and may function as a tumor suppressor. A chromosomal rearrangement resulting in the expression of a fusion gene containing a portion of this gene and the intracellular kinase-encoding domain of the ret proto-oncogene is the cause of thyroid papillary carcinoma.[provided by RefSeq, Sep 2010]","start":59788763,"end":59906656,"strand":-1,"description":"coiled-coil domain containing 6 [Source:HGNC Symbol;Acc:HGNC:18782]"}, {"versioned_ensembl_gene_id":"ENSG00000237843.1","gene_symbol":"AC016903.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204475356,"end":204507672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184508.10","gene_symbol":"HDDC3","gene_name":"HD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30522]","synonyms":"MGC45386","biotype":"protein_coding","ncbi_id":"374659","summary":null,"start":90929964,"end":90932569,"strand":-1,"description":"HD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30522]"}, {"versioned_ensembl_gene_id":"ENSG00000226187.8","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31703097,"end":31704573,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000125618.16","gene_symbol":"PAX8","gene_name":"paired box 8 [Source:HGNC Symbol;Acc:HGNC:8622]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7849","summary":"This gene encodes a member of the paired box (PAX) family of transcription factors. Members of this gene family typically encode proteins that contain a paired box domain, an octapeptide, and a paired-type homeodomain. This nuclear protein is involved in thyroid follicular cell development and expression of thyroid-specific genes. Mutations in this gene have been associated with thyroid dysgenesis, thyroid follicular carcinomas and atypical follicular thyroid adenomas. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]","start":113215997,"end":113278950,"strand":-1,"description":"paired box 8 [Source:HGNC Symbol;Acc:HGNC:8622]"}, {"versioned_ensembl_gene_id":"ENSG00000230509.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30341669,"end":30341803,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000239457.6","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32903640,"end":32907925,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000135587.8","gene_symbol":"SMPD2","gene_name":"sphingomyelin phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:11121]","synonyms":"nSMase,ISC1","biotype":"protein_coding","ncbi_id":"6610","summary":"This gene encodes a protein which was initially identified as a sphingomyelinase based on sequence similarity between bacterial sphingomyelinases and a yeast protein. Subsequent studies showed that its biological function is less likely to be as a sphingomyelinase and instead as a lysophospholipase. [provided by RefSeq, Oct 2009]","start":109440763,"end":109443919,"strand":1,"description":"sphingomyelin phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:11121]"}, {"versioned_ensembl_gene_id":"ENSG00000229352.1","gene_symbol":"AC007563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":216799608,"end":216805335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102053.12","gene_symbol":"ZC3H12B","gene_name":"zinc finger CCCH-type containing 12B [Source:HGNC Symbol;Acc:HGNC:17407]","synonyms":"MCPIP2,CXorf32","biotype":"protein_coding","ncbi_id":"340554","summary":"The protein encoded by this gene belongs to a family of CCCH-type zinc finger proteins that are involved in the proinflammatory activation of macrophages. The exact function of this family member is unknown, but it is thought to function as a ribonuclease. [provided by RefSeq, May 2010]","start":65366638,"end":65507887,"strand":1,"description":"zinc finger CCCH-type containing 12B [Source:HGNC Symbol;Acc:HGNC:17407]"}, {"versioned_ensembl_gene_id":"ENSG00000256019.1","gene_symbol":"AC018630.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11048332,"end":11049256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229437.1","gene_symbol":"LINC00366","gene_name":"long intergenic non-protein coding RNA 366 [Source:HGNC Symbol;Acc:HGNC:42688]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874147","summary":null,"start":38576640,"end":38578994,"strand":1,"description":"long intergenic non-protein coding RNA 366 [Source:HGNC Symbol;Acc:HGNC:42688]"}, {"versioned_ensembl_gene_id":"ENSG00000174885.12","gene_symbol":"NLRP6","gene_name":"NLR family pyrin domain containing 6 [Source:HGNC Symbol;Acc:HGNC:22944]","synonyms":"PYPAF5,PAN3,NALP6,CLR11.4","biotype":"protein_coding","ncbi_id":"171389","summary":"The protein encoded by this gene binds arginine-vasopressin and may be involved in the arginine-vasopressin-mediated regulation of renal salt-water balance. The encoded protein also mediates inflammatory responses in the colon to allow recovery from intestinal epithelial damage and protects against tumorigenesis and the development of colitis. Finally, this protein can increase activation of NF-kappa-B, activation of CASP1 through interaction with ASC, and cAMP accumulation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":278365,"end":285359,"strand":1,"description":"NLR family pyrin domain containing 6 [Source:HGNC Symbol;Acc:HGNC:22944]"}, {"versioned_ensembl_gene_id":"ENSG00000213498.3","gene_symbol":"TPT1P13","gene_name":"tumor protein, translationally-controlled 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49304]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643421","summary":null,"start":121863698,"end":121864196,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49304]"}, {"versioned_ensembl_gene_id":"ENSG00000226091.7","gene_symbol":"LINC00937","gene_name":"long intergenic non-protein coding RNA 937 [Source:HGNC Symbol;Acc:HGNC:48629]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389634","summary":null,"start":8295986,"end":8396803,"strand":-1,"description":"long intergenic non-protein coding RNA 937 [Source:HGNC Symbol;Acc:HGNC:48629]"}, {"versioned_ensembl_gene_id":"ENSG00000179958.8","gene_symbol":"DCTPP1","gene_name":"dCTP pyrophosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28777]","synonyms":"XTP3TPA,RS21C6,MGC5627,CDA03","biotype":"protein_coding","ncbi_id":"79077","summary":"The protein encoded by this gene is dCTP pyrophosphatase, which converts dCTP to dCMP and inorganic pyrophosphate. The encoded protein also displays weak activity against dTTP and dATP, but none against dGTP. This protein may be responsible for eliminating excess dCTP after DNA synthesis and may prevent overmethylation of CpG islands. Three transcript variants, one protein-coding and the other two non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]","start":30423619,"end":30430075,"strand":-1,"description":"dCTP pyrophosphatase 1 [Source:HGNC Symbol;Acc:HGNC:28777]"}, {"versioned_ensembl_gene_id":"ENSG00000254425.1","gene_symbol":"AC022690.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13909231,"end":13909780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253418.1","gene_symbol":"SNX18P27","gene_name":"sorting nexin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39635]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873788","summary":null,"start":43513643,"end":43514421,"strand":1,"description":"sorting nexin 18 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:39635]"}, {"versioned_ensembl_gene_id":"ENSG00000229939.1","gene_symbol":"AL589880.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111618808,"end":111619094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204919.1","gene_symbol":"PRR20A","gene_name":"proline rich 20A [Source:HGNC Symbol;Acc:HGNC:24754]","synonyms":"PRR20,FLJ40296","biotype":"protein_coding","ncbi_id":"122183","summary":"This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008]","start":57140918,"end":57143939,"strand":1,"description":"proline rich 20A [Source:HGNC Symbol;Acc:HGNC:24754]"}, {"versioned_ensembl_gene_id":"ENSG00000226661.1","gene_symbol":"AC004973.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119356301,"end":119393595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236395.1","gene_symbol":"AC093106.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131702269,"end":131702653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271806.1","gene_symbol":"AL590822.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2141084,"end":2145279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175664.9","gene_symbol":"TEX26","gene_name":"testis expressed 26 [Source:HGNC Symbol;Acc:HGNC:28622]","synonyms":"MGC40178,C13orf26","biotype":"protein_coding","ncbi_id":"122046","summary":null,"start":30932703,"end":30975502,"strand":1,"description":"testis expressed 26 [Source:HGNC Symbol;Acc:HGNC:28622]"}, {"versioned_ensembl_gene_id":"ENSG00000283003.1","gene_symbol":"AC007221.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9542045,"end":9614894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261740.6","gene_symbol":"BOLA2-SMG1P6","gene_name":"BOLA2-SMG1P6 readthrough [Source:HGNC Symbol;Acc:HGNC:53563]","synonyms":null,"biotype":"protein_coding","ncbi_id":"107282092","summary":"This gene represents naturally-occurring readthrough transcription between the upstream BOLA2 (bolA family member 2) and downstream SMG1 pseudogene 6 (SMG1P6) loci. Alternative splicing results in multiple transcript variants, some of which may encode proteins with an N-terminus similar to BOLA2 and a C-terminus related to SMG1 phosphatidylinositol 3-kinase-related kinase. [provided by RefSeq, Feb 2016]","start":29443230,"end":29454651,"strand":-1,"description":"BOLA2-SMG1P6 readthrough [Source:HGNC Symbol;Acc:HGNC:53563]"}, {"versioned_ensembl_gene_id":"ENSG00000254499.1","gene_symbol":"AC002056.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50740593,"end":50743520,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133059.16","gene_symbol":"DSTYK","gene_name":"dual serine/threonine and tyrosine protein kinase [Source:HGNC Symbol;Acc:HGNC:29043]","synonyms":"RIPK5,RIP5,KIAA0472,DustyPK","biotype":"protein_coding","ncbi_id":"25778","summary":"This gene encodes a dual serine/threonine and tyrosine protein kinase which is expressed in multiple tissues. It is thought to function as a regulator of cell death. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":205142505,"end":205211566,"strand":-1,"description":"dual serine/threonine and tyrosine protein kinase [Source:HGNC Symbol;Acc:HGNC:29043]"}, {"versioned_ensembl_gene_id":"ENSG00000230387.2","gene_symbol":"AL118508.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23187961,"end":23190307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169429.10","gene_symbol":"CXCL8","gene_name":"C-X-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:6025]","synonyms":"LUCT,LECT,K60,IL8,IL-8,GCP1,GCP-1,b-ENAP,AMCF-I,TSG-1,3-10C,SCYB8,NAP1,NAP-1,NAF,MONAP,MDNCF,LYNAP","biotype":"protein_coding","ncbi_id":"3576","summary":"The protein encoded by this gene is a member of the CXC chemokine family and is a major mediator of the inflammatory response. The encoded protein is commonly referred to as interleukin-8 (IL-8). IL-8 is secreted by mononuclear macrophages, neutrophils, eosinophils, T lymphocytes, epithelial cells, and fibroblasts. It functions as a chemotactic factor by guiding the neutrophils to the site of infection. Bacterial and viral products rapidly induce IL-8 expression. IL-8 also participates with other cytokines in the proinflammatory signaling cascade and plays a role in systemic inflammatory response syndrome (SIRS). This gene is believed to play a role in the pathogenesis of the lower respiratory tract infection bronchiolitis, a common respiratory tract disease caused by the respiratory syncytial virus (RSV). The overproduction of this proinflammatory protein is thought to cause the lung inflammation associated with csytic fibrosis. This proinflammatory protein is also suspected of playing a role in coronary artery disease and endothelial dysfunction. This protein is also secreted by tumor cells and promotes tumor migration, invasion, angiogenesis and metastasis. This chemokine is also a potent angiogenic factor. The binding of IL-8 to one of its receptors (IL-8RB/CXCR2) increases the permeability of blood vessels and increasing levels of IL-8 are positively correlated with increased severity of multiple disease outcomes (eg, sepsis). This gene and other members of the CXC chemokine gene family form a gene cluster in a region of chromosome 4q. [provided by RefSeq, May 2020]","start":73740506,"end":73743716,"strand":1,"description":"C-X-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:6025]"}, {"versioned_ensembl_gene_id":"ENSG00000162494.5","gene_symbol":"LRRC38","gene_name":"leucine rich repeat containing 38 [Source:HGNC Symbol;Acc:HGNC:27005]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126755","summary":null,"start":13474977,"end":13514048,"strand":-1,"description":"leucine rich repeat containing 38 [Source:HGNC Symbol;Acc:HGNC:27005]"}, {"versioned_ensembl_gene_id":"ENSG00000218672.1","gene_symbol":"AC008060.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155382076,"end":155396356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079819.18","gene_symbol":"EPB41L2","gene_name":"erythrocyte membrane protein band 4.1 like 2 [Source:HGNC Symbol;Acc:HGNC:3379]","synonyms":"4.1-G","biotype":"protein_coding","ncbi_id":"2037","summary":null,"start":130839347,"end":131063322,"strand":-1,"description":"erythrocyte membrane protein band 4.1 like 2 [Source:HGNC Symbol;Acc:HGNC:3379]"}, {"versioned_ensembl_gene_id":"ENSG00000261404.6","gene_symbol":"AC138627.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73943078,"end":74296762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158528.11","gene_symbol":"PPP1R9A","gene_name":"protein phosphatase 1 regulatory subunit 9A [Source:HGNC Symbol;Acc:HGNC:14946]","synonyms":"Neurabin-I,KIAA1222,FLJ20068","biotype":"protein_coding","ncbi_id":"55607","summary":"This gene is imprinted, and located in a cluster of imprinted genes on chromosome 7q12. This gene is transcribed in both neuronal and multiple embryonic tissues, and it is maternally expressed mainly in embryonic skeletal muscle tissues and biallelically expressed in other embryonic tissues. The protein encoded by this gene includes a PDZ domain and a sterile alpha motif (SAM). It is a regulatory subunit of protein phosphatase I, and controls actin cytoskeleton reorganization. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":94907202,"end":95296415,"strand":1,"description":"protein phosphatase 1 regulatory subunit 9A [Source:HGNC Symbol;Acc:HGNC:14946]"}, {"versioned_ensembl_gene_id":"ENSG00000213536.2","gene_symbol":"GNG5P1","gene_name":"G protein subunit gamma 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4409]","synonyms":"GNG5P","biotype":"processed_pseudogene","ncbi_id":"2789","summary":null,"start":166240290,"end":166240493,"strand":-1,"description":"G protein subunit gamma 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4409]"}, {"versioned_ensembl_gene_id":"ENSG00000233365.2","gene_symbol":"AL121956.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166236969,"end":166256947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282561.1","gene_symbol":"IGHV1-17","gene_name":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28469","summary":null,"start":106175113,"end":106175531,"strand":-1,"description":"immunoglobulin heavy variable 1-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5548]"}, {"versioned_ensembl_gene_id":"ENSG00000223364.1","gene_symbol":"PSORS1C3","gene_name":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]","synonyms":"NCRNA00196","biotype":"processed_transcript","ncbi_id":"100130889","summary":null,"start":31166295,"end":31170460,"strand":-1,"description":"psoriasis susceptibility 1 candidate 3 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17203]"}, {"versioned_ensembl_gene_id":"ENSG00000124523.15","gene_symbol":"SIRT5","gene_name":"sirtuin 5 [Source:HGNC Symbol;Acc:HGNC:14933]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23408","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class III of the sirtuin family. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":13574529,"end":13615158,"strand":1,"description":"sirtuin 5 [Source:HGNC Symbol;Acc:HGNC:14933]"}, {"versioned_ensembl_gene_id":"ENSG00000026950.16","gene_symbol":"BTN3A1","gene_name":"butyrophilin subfamily 3 member A1 [Source:HGNC Symbol;Acc:HGNC:1138]","synonyms":"CD277,BTN3.1,BTF5,BT3.1","biotype":"protein_coding","ncbi_id":"11119","summary":"The butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC)-associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30.2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single-copy BTN1A1 gene (MIM 601610) and the BTN2 (e.g., BTN2A1; MIM 613590) and BTN3 (e.g., BNT3A1) genes, which have undergone tandem duplication, resulting in 3 copies of each (summary by Smith et al., 2010 [PubMed 20208008]).[supplied by OMIM, Nov 2010]","start":26402237,"end":26415216,"strand":1,"description":"butyrophilin subfamily 3 member A1 [Source:HGNC Symbol;Acc:HGNC:1138]"}, {"versioned_ensembl_gene_id":"ENSG00000251656.1","gene_symbol":"PRELID3BP5","gene_name":"PRELI domain containing 3B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49067]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480242","summary":null,"start":42908208,"end":42908667,"strand":-1,"description":"PRELI domain containing 3B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49067]"}, {"versioned_ensembl_gene_id":"ENSG00000227855.3","gene_symbol":"DPY19L2P3","gene_name":"DPY19L2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22367]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442524","summary":null,"start":29650227,"end":29742594,"strand":1,"description":"DPY19L2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:22367]"}, {"versioned_ensembl_gene_id":"ENSG00000128829.11","gene_symbol":"EIF2AK4","gene_name":"eukaryotic translation initiation factor 2 alpha kinase 4 [Source:HGNC Symbol;Acc:HGNC:19687]","synonyms":"KIAA1338,GCN2","biotype":"protein_coding","ncbi_id":"440275","summary":"This gene encodes a member of a family of kinases that phosphorylate the alpha subunit of eukaryotic translation initiation factor-2 (EIF2), resulting in the downregulaton of protein synthesis. The encoded protein responds to amino acid deprivation by binding uncharged transfer RNAs. It may also be activated by glucose deprivation and viral infection. Mutations in this gene have been found in individuals suffering from autosomal recessive pulmonary venoocclusive-disease-2. [provided by RefSeq, Mar 2014]","start":39934146,"end":40035591,"strand":1,"description":"eukaryotic translation initiation factor 2 alpha kinase 4 [Source:HGNC Symbol;Acc:HGNC:19687]"}, {"versioned_ensembl_gene_id":"ENSG00000258288.1","gene_symbol":"NENFP2","gene_name":"neudesin neurotrophic factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50299]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129880","summary":null,"start":101963901,"end":101964340,"strand":1,"description":"neudesin neurotrophic factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50299]"}, {"versioned_ensembl_gene_id":"ENSG00000258215.1","gene_symbol":"AC078886.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80860955,"end":80861508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237890.5","gene_symbol":"BX571801.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30790867,"end":30822832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111424.10","gene_symbol":"VDR","gene_name":"vitamin D receptor [Source:HGNC Symbol;Acc:HGNC:12679]","synonyms":"PPP1R163,NR1I1","biotype":"protein_coding","ncbi_id":"7421","summary":"This gene encodes vitamin D3 receptor, which is a member of the nuclear hormone receptor superfamily of ligand-inducible transcription factors. This receptor also functions as a receptor for the secondary bile acid, lithocholic acid. Downstream targets of vitamin D3 receptor are principally involved in mineral metabolism, though this receptor regulates a variety of other metabolic pathways, such as those involved in immune response and cancer. Mutations in this gene are associated with type II vitamin D-resistant rickets. A single nucleotide polymorphism in the initiation codon results in an alternate translation start site three codons downstream. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Jun 2018]","start":47841537,"end":47943048,"strand":-1,"description":"vitamin D receptor [Source:HGNC Symbol;Acc:HGNC:12679]"}, {"versioned_ensembl_gene_id":"ENSG00000155096.13","gene_symbol":"AZIN1","gene_name":"antizyme inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:16432]","synonyms":"ODC1L,OAZIN,OAZI","biotype":"protein_coding","ncbi_id":"51582","summary":"The protein encoded by this gene belongs to the antizyme inhibitor family, which plays a role in cell growth and proliferation by maintaining polyamine homeostasis within the cell. Antizyme inhibitors are homologs of ornithine decarboxylase (ODC, the key enzyme in polyamine biosynthesis) that have lost the ability to decarboxylase ornithine; however, retain the ability to bind to antizymes. Antizymes negatively regulate intracellular polyamine levels by binding to ODC and targeting it for degradation, as well as by inhibiting polyamine uptake. Antizyme inhibitors function as positive regulators of polyamine levels by sequestering antizymes and neutralizing their effect. This gene encodes antizyme inhibitor 1, the first member of this gene family that is ubiquitously expressed, and is localized in the nucleus and cytoplasm. Overexpression of antizyme inhibitor 1 gene has been associated with increased proliferation, cellular transformation and tumorigenesis. Gene knockout studies showed that homozygous mutant mice lacking functional antizyme inhibitor 1 gene died at birth with abnormal liver morphology. RNA editing of this gene, predominantly in the liver tissue, has been linked to the progression of hepatocellular carcinoma. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2014]","start":102826357,"end":102893864,"strand":-1,"description":"antizyme inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:16432]"}, {"versioned_ensembl_gene_id":"ENSG00000237971.1","gene_symbol":"AL445523.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65185018,"end":65187265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203926.4","gene_symbol":"SPANXA2","gene_name":"SPANX family member A2 [Source:HGNC Symbol;Acc:HGNC:14328]","synonyms":"SPANX","biotype":"protein_coding","ncbi_id":"728712","summary":"Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene maps to chromosome X in a head-to-head orientation with SPANX family member A1 and appears to be a duplication of that locus. The protein encoded by this gene targets to the nucleus where it associates with nuclear vacuoles and the redundant nuclear envelope. Based on its association with these poorly characterized regions of the sperm nucleus, this protein provides a biochemical marker to study unique structures in spermatazoa while attempting to further define its role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":141589435,"end":141590772,"strand":1,"description":"SPANX family member A2 [Source:HGNC Symbol;Acc:HGNC:14328]"}, {"versioned_ensembl_gene_id":"ENSG00000065989.15","gene_symbol":"PDE4A","gene_name":"phosphodiesterase 4A [Source:HGNC Symbol;Acc:HGNC:8780]","synonyms":"DPDE2","biotype":"protein_coding","ncbi_id":"5141","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE4 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":10416773,"end":10469631,"strand":1,"description":"phosphodiesterase 4A [Source:HGNC Symbol;Acc:HGNC:8780]"}, {"versioned_ensembl_gene_id":"ENSG00000236862.1","gene_symbol":"RPS20P24","gene_name":"ribosomal protein S20 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36283]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271232","summary":null,"start":72655832,"end":72656192,"strand":-1,"description":"ribosomal protein S20 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36283]"}, {"versioned_ensembl_gene_id":"ENSG00000271154.1","gene_symbol":"AL670379.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120942623,"end":120942875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177738.3","gene_symbol":"AC025171.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":43014414,"end":43067419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233670.6","gene_symbol":"PIRT","gene_name":"phosphoinositide interacting regulator of transient receptor potential channels [Source:HGNC Symbol;Acc:HGNC:37239]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644139","summary":null,"start":10822475,"end":10838445,"strand":-1,"description":"phosphoinositide interacting regulator of transient receptor potential channels [Source:HGNC Symbol;Acc:HGNC:37239]"}, {"versioned_ensembl_gene_id":"ENSG00000236093.1","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32801489,"end":32802166,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000234067.1","gene_symbol":"RPL5P10","gene_name":"ribosomal protein L5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36846]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645807","summary":null,"start":40586535,"end":40587428,"strand":-1,"description":"ribosomal protein L5 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36846]"}, {"versioned_ensembl_gene_id":"ENSG00000131779.10","gene_symbol":"PEX11B","gene_name":"peroxisomal biogenesis factor 11 beta [Source:HGNC Symbol;Acc:HGNC:8853]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8799","summary":"The protein encoded by this gene facilitates peroxisomal proliferation and interacts with PEX19. The encoded protein is found in the peroxisomal membrane. Several transcript variants, some protein-coding and some not protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012]","start":145911350,"end":145918837,"strand":-1,"description":"peroxisomal biogenesis factor 11 beta [Source:HGNC Symbol;Acc:HGNC:8853]"}, {"versioned_ensembl_gene_id":"ENSG00000101452.14","gene_symbol":"DHX35","gene_name":"DEAH-box helicase 35 [Source:HGNC Symbol;Acc:HGNC:15861]","synonyms":"KAIA0875,FLJ22759,DDX35,C20orf15","biotype":"protein_coding","ncbi_id":"60625","summary":"DEAD box proteins characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The function of this gene product which is a member of this family, has not been determined. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2010]","start":38962299,"end":39039723,"strand":1,"description":"DEAH-box helicase 35 [Source:HGNC Symbol;Acc:HGNC:15861]"}, {"versioned_ensembl_gene_id":"ENSG00000223984.1","gene_symbol":"HNRNPRP1","gene_name":"heterogeneous nuclear ribonucleoprotein R pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44907]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100125387","summary":null,"start":21624592,"end":21626286,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein R pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44907]"}, {"versioned_ensembl_gene_id":"ENSG00000280825.1","gene_symbol":"IGLV7-35","gene_name":"immunoglobulin lambda variable 7-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5928]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28777","summary":null,"start":22459289,"end":22459739,"strand":1,"description":"immunoglobulin lambda variable 7-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5928]"}, {"versioned_ensembl_gene_id":"ENSG00000235715.6","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32763034,"end":32767021,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000142871.16","gene_symbol":"CYR61","gene_name":"cysteine rich angiogenic inducer 61 [Source:HGNC Symbol;Acc:HGNC:2654]","synonyms":"CCN1,IGFBP10,GIG1","biotype":"protein_coding","ncbi_id":"3491","summary":"The secreted protein encoded by this gene is growth factor-inducible and promotes the adhesion of endothelial cells. The encoded protein interacts with several integrins and with heparan sulfate proteoglycan. This protein also plays a role in cell proliferation, differentiation, angiogenesis, apoptosis, and extracellular matrix formation. [provided by RefSeq, Sep 2011]","start":85580761,"end":85583962,"strand":1,"description":"cysteine rich angiogenic inducer 61 [Source:HGNC Symbol;Acc:HGNC:2654]"}, {"versioned_ensembl_gene_id":"ENSG00000276172.1","gene_symbol":"ELMO2P1","gene_name":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729894","summary":null,"start":23083094,"end":23121324,"strand":1,"description":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]"}, {"versioned_ensembl_gene_id":"ENSG00000214925.3","gene_symbol":"AC234778.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141138478,"end":141139174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231261.1","gene_symbol":"HMGN2P10","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene10 [Source:HGNC Symbol;Acc:HGNC:4988]","synonyms":"HMGN2L10,HMG17L2,bK216E10","biotype":"processed_pseudogene","ncbi_id":"23606","summary":null,"start":41709225,"end":41709489,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene10 [Source:HGNC Symbol;Acc:HGNC:4988]"}, {"versioned_ensembl_gene_id":"ENSG00000246863.2","gene_symbol":"AC012377.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39921042,"end":39925880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272831.1","gene_symbol":"AC027644.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66739829,"end":66740385,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219159.4","gene_symbol":"AC011298.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":240686334,"end":240690414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234579.1","gene_symbol":"AC009305.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30986939,"end":30991426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267760.1","gene_symbol":"AC011478.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30665274,"end":30668647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282650.1","gene_symbol":"MEIOB","gene_name":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]","synonyms":"MGC35212,C16orf73","biotype":"processed_transcript","ncbi_id":"254528","summary":null,"start":1874025,"end":1886319,"strand":-1,"description":"meiosis specific with OB domains [Source:HGNC Symbol;Acc:HGNC:28569]"}, {"versioned_ensembl_gene_id":"ENSG00000248430.1","gene_symbol":"HMGB3P16","gene_name":"high mobility group box 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39308]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873900","summary":null,"start":112452703,"end":112452989,"strand":-1,"description":"high mobility group box 3 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:39308]"}, {"versioned_ensembl_gene_id":"ENSG00000232568.2","gene_symbol":"RPL23AP35","gene_name":"ribosomal protein L23a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36580]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271295","summary":null,"start":186261419,"end":186261919,"strand":-1,"description":"ribosomal protein L23a pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36580]"}, {"versioned_ensembl_gene_id":"ENSG00000236688.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30340905,"end":30341039,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000274746.4","gene_symbol":"ZNF100","gene_name":"zinc finger protein 100 [Source:HGNC Symbol;Acc:HGNC:12880]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163227","summary":null,"start":21732245,"end":21777028,"strand":-1,"description":"zinc finger protein 100 [Source:HGNC Symbol;Acc:HGNC:12880]"}, {"versioned_ensembl_gene_id":"ENSG00000196220.15","gene_symbol":"SRGAP3","gene_name":"SLIT-ROBO Rho GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:19744]","synonyms":"WRP,SRGAP2,MEGAP,KIAA0411,ARHGAP14","biotype":"protein_coding","ncbi_id":"9901","summary":null,"start":8980591,"end":9363053,"strand":-1,"description":"SLIT-ROBO Rho GTPase activating protein 3 [Source:HGNC Symbol;Acc:HGNC:19744]"}, {"versioned_ensembl_gene_id":"ENSG00000280218.1","gene_symbol":"VN1R84P","gene_name":"vomeronasal 1 receptor 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:37404]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312829","summary":null,"start":21729280,"end":21729514,"strand":-1,"description":"vomeronasal 1 receptor 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:37404]"}, {"versioned_ensembl_gene_id":"ENSG00000280137.1","gene_symbol":"AC116348.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30379763,"end":30380110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232046.6","gene_symbol":"LINC01798","gene_name":"long intergenic non-protein coding RNA 1798 [Source:HGNC Symbol;Acc:HGNC:52588]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507073","summary":null,"start":66574030,"end":66730157,"strand":1,"description":"long intergenic non-protein coding RNA 1798 [Source:HGNC Symbol;Acc:HGNC:52588]"}, {"versioned_ensembl_gene_id":"ENSG00000111670.14","gene_symbol":"GNPTAB","gene_name":"N-acetylglucosamine-1-phosphate transferase alpha and beta subunits [Source:HGNC Symbol;Acc:HGNC:29670]","synonyms":"MGC4170,KIAA1208,GNPTA","biotype":"protein_coding","ncbi_id":"79158","summary":"This gene encodes two of three subunit types of the membrane-bound enzyme N-acetylglucosamine-1-phosphotransferase, a heterohexameric complex composed of two alpha, two beta, and two gamma subunits. The encoded protein is proteolytically cleaved at the Lys928-Asp929 bond to yield mature alpha and beta polypeptides while the gamma subunits are the product of a distinct gene (GeneID 84572). In the Golgi apparatus, the heterohexameric complex catalyzes the first step in the synthesis of mannose 6-phosphate recognition markers on certain oligosaccharides of newly synthesized lysosomal enzymes. These recognition markers are essential for appropriate trafficking of lysosomal enzymes. Mutations in this gene have been associated with both mucolipidosis II and mucolipidosis IIIA.[provided by RefSeq, May 2010]","start":101745497,"end":101830938,"strand":-1,"description":"N-acetylglucosamine-1-phosphate transferase alpha and beta subunits [Source:HGNC Symbol;Acc:HGNC:29670]"}, {"versioned_ensembl_gene_id":"ENSG00000273384.1","gene_symbol":"AL137796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178651706,"end":178652282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105397.13","gene_symbol":"TYK2","gene_name":"tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:12440]","synonyms":"JTK1","biotype":"protein_coding","ncbi_id":"7297","summary":"This gene encodes a member of the tyrosine kinase and, more specifically, the Janus kinases (JAKs) protein families. This protein associates with the cytoplasmic domain of type I and type II cytokine receptors and promulgate cytokine signals by phosphorylating receptor subunits. It is also a component of both the type I and type III interferon signaling pathways. As such, it may play a role in anti-viral immunity. A mutation in this gene has been associated with Immunodeficiency 35. [provided by RefSeq, Sep 2020]","start":10350529,"end":10380676,"strand":-1,"description":"tyrosine kinase 2 [Source:HGNC Symbol;Acc:HGNC:12440]"}, {"versioned_ensembl_gene_id":"ENSG00000270898.5","gene_symbol":"GPR75-ASB3","gene_name":"GPR75-ASB3 readthrough [Source:HGNC Symbol;Acc:HGNC:40043]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100302652","summary":"This locus represents naturally occurring read-through transcription between the neighboring GPR75 (G protein-coupled receptor 75) and ASB3 (ankyrin repeat and SOCS box containing 3) on chromosome 2. The transcript includes exons from both GPR75 and ASB3 and translation initiates in the 5' non-coding exon of GPR75. The resulting protein has a novel N-terminus but is otherwise identical to that encoded by ASB3.[provided by RefSeq, Feb 2011]","start":53670293,"end":53860160,"strand":-1,"description":"GPR75-ASB3 readthrough [Source:HGNC Symbol;Acc:HGNC:40043]"}, {"versioned_ensembl_gene_id":"ENSG00000228775.7","gene_symbol":"WEE2-AS1","gene_name":"WEE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48669]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285962","summary":null,"start":141704338,"end":141738346,"strand":-1,"description":"WEE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48669]"}, {"versioned_ensembl_gene_id":"ENSG00000260413.1","gene_symbol":"AC025279.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29312350,"end":29331277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138190.16","gene_symbol":"EXOC6","gene_name":"exocyst complex component 6 [Source:HGNC Symbol;Acc:HGNC:23196]","synonyms":"Sec15p,SEC15L1,SEC15L,MGC33397,FLJ1125,EXOC6A,DKFZp761I2124","biotype":"protein_coding","ncbi_id":"54536","summary":"The protein encoded by this gene is highly similar to the Saccharomyces cerevisiae SEC15 gene product, which is essential for vesicular traffic from the Golgi apparatus to the cell surface in yeast. It is one of the components of a multiprotein complex required for exocytosis. The 5' portion of this gene and two neighboring cytochrome p450 genes are included in a deletion that results in an autosomal-dominant form of nonsyndromic optic nerve aplasia (ONA). Alternative splicing and the use of alternative promoters results in multiple transcript variants. A paralogous gene encoding a similar protein is present on chromosome 2. [provided by RefSeq, Jan 2016]","start":92834713,"end":93059493,"strand":1,"description":"exocyst complex component 6 [Source:HGNC Symbol;Acc:HGNC:23196]"}, {"versioned_ensembl_gene_id":"ENSG00000066248.14","gene_symbol":"NGEF","gene_name":"neuronal guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:7807]","synonyms":"ARHGEF27","biotype":"protein_coding","ncbi_id":"25791","summary":null,"start":232878686,"end":233013272,"strand":-1,"description":"neuronal guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:7807]"}, {"versioned_ensembl_gene_id":"ENSG00000106392.10","gene_symbol":"C1GALT1","gene_name":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24337]","synonyms":"T-synthase,C1GALT","biotype":"protein_coding","ncbi_id":"56913","summary":"The protein encoded by this gene generates the common core 1 O-glycan structure, Gal-beta-1-3GalNAc-R, by the transfer of Gal from UDP-Gal to GalNAc-alpha-1-R. Core 1 is a precursor for many extended mucin-type O-glycans on cell surface and secreted glycoproteins. Studies in mice suggest that this gene plays a key role in thrombopoiesis and kidney homeostasis.[provided by RefSeq, Sep 2010]","start":7156934,"end":7248651,"strand":1,"description":"core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:24337]"}, {"versioned_ensembl_gene_id":"ENSG00000124713.5","gene_symbol":"GNMT","gene_name":"glycine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4415]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27232","summary":"The protein encoded by this gene is an enzyme that catalyzes the conversion of S-adenosyl-L-methionine (along with glycine) to S-adenosyl-L-homocysteine and sarcosine. This protein is found in the cytoplasm and acts as a homotetramer. Defects in this gene are a cause of GNMT deficiency (hypermethioninemia). Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between the upstream CNPY3 (canopy FGF signaling regulator 3) gene and this gene and is represented with GeneID:107080644. [provided by RefSeq, Jan 2016]","start":42960758,"end":42963880,"strand":1,"description":"glycine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:4415]"}, {"versioned_ensembl_gene_id":"ENSG00000250325.1","gene_symbol":"IGBP1P4","gene_name":"immunoglobulin (CD79A) binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43613]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391672","summary":null,"start":82401578,"end":82402456,"strand":-1,"description":"immunoglobulin (CD79A) binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43613]"}, {"versioned_ensembl_gene_id":"ENSG00000281074.1","gene_symbol":"IGLVVII-41-1","gene_name":"immunoglobulin lambda variable (VII)-41-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15691]","synonyms":"IGLV(VII)-41-1","biotype":"IG_V_pseudogene","ncbi_id":"84089","summary":null,"start":22407947,"end":22408097,"strand":1,"description":"immunoglobulin lambda variable (VII)-41-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15691]"}, {"versioned_ensembl_gene_id":"ENSG00000169325.10","gene_symbol":"GUSBP12","gene_name":"glucuronidase, beta pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42326]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"642007","summary":null,"start":57200825,"end":57203597,"strand":-1,"description":"glucuronidase, beta pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42326]"}, {"versioned_ensembl_gene_id":"ENSG00000213281.4","gene_symbol":"NRAS","gene_name":"NRAS proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:7989]","synonyms":"N-ras","biotype":"protein_coding","ncbi_id":"4893","summary":"This is an N-ras oncogene encoding a membrane protein that shuttles between the Golgi apparatus and the plasma membrane. This shuttling is regulated through palmitoylation and depalmitoylation by the ZDHHC9-GOLGA7 complex. The encoded protein, which has intrinsic GTPase activity, is activated by a guanine nucleotide-exchange factor and inactivated by a GTPase activating protein. Mutations in this gene have been associated with somatic rectal cancer, follicular thyroid cancer, autoimmune lymphoproliferative syndrome, Noonan syndrome, and juvenile myelomonocytic leukemia. [provided by RefSeq, Jun 2011]","start":114704469,"end":114716894,"strand":-1,"description":"NRAS proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:7989]"}, {"versioned_ensembl_gene_id":"ENSG00000132965.9","gene_symbol":"ALOX5AP","gene_name":"arachidonate 5-lipoxygenase activating protein [Source:HGNC Symbol;Acc:HGNC:436]","synonyms":"FLAP","biotype":"protein_coding","ncbi_id":"241","summary":"This gene encodes a protein which, with 5-lipoxygenase, is required for leukotriene synthesis. Leukotrienes are arachidonic acid metabolites which have been implicated in various types of inflammatory responses, including asthma, arthritis and psoriasis. This protein localizes to the plasma membrane. Inhibitors of its function impede translocation of 5-lipoxygenase from the cytoplasm to the cell membrane and inhibit 5-lipoxygenase activation. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Feb 2011]","start":30713478,"end":30764426,"strand":1,"description":"arachidonate 5-lipoxygenase activating protein [Source:HGNC Symbol;Acc:HGNC:436]"}, {"versioned_ensembl_gene_id":"ENSG00000277529.1","gene_symbol":"NF1P10","gene_name":"neurofibromin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51737]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106480348","summary":null,"start":18709478,"end":18712643,"strand":-1,"description":"neurofibromin 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51737]"}, {"versioned_ensembl_gene_id":"ENSG00000114383.9","gene_symbol":"TUSC2","gene_name":"tumor suppressor candidate 2 [Source:HGNC Symbol;Acc:HGNC:17034]","synonyms":"PDAP2,PAP,FUS1,C3orf11","biotype":"protein_coding","ncbi_id":"11334","summary":"This gene is a highly conserved lung cancer candidate gene. No other information about this gene is currently available. [provided by RefSeq, Jul 2008]","start":50320027,"end":50328251,"strand":-1,"description":"tumor suppressor candidate 2 [Source:HGNC Symbol;Acc:HGNC:17034]"}, {"versioned_ensembl_gene_id":"ENSG00000162241.12","gene_symbol":"SLC25A45","gene_name":"solute carrier family 25 member 45 [Source:HGNC Symbol;Acc:HGNC:27442]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283130","summary":"SLC25A45 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":65375192,"end":65383701,"strand":-1,"description":"solute carrier family 25 member 45 [Source:HGNC Symbol;Acc:HGNC:27442]"}, {"versioned_ensembl_gene_id":"ENSG00000261706.1","gene_symbol":"AP001505.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44994362,"end":44995185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214413.7","gene_symbol":"BBIP1","gene_name":"BBSome interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:28093]","synonyms":"NCRNA00081,BBS18,BBIP10,bA348N5.3","biotype":"protein_coding","ncbi_id":"92482","summary":"This gene encodes one of eight proteins that form the BBSome complex and is essential for its assembly. The BBSome complex is involved in trafficking signal receptors to and from the cilia. Mutations in this gene result in Bardet-Biedl syndrome 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":110898730,"end":110919274,"strand":-1,"description":"BBSome interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:28093]"}, {"versioned_ensembl_gene_id":"ENSG00000283415.1","gene_symbol":"AC087280.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6821942,"end":6926877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166368.2","gene_symbol":"OR2D2","gene_name":"olfactory receptor family 2 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8244]","synonyms":"hg27,OR2D1,OR11-610","biotype":"protein_coding","ncbi_id":"120776","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6891490,"end":6892599,"strand":-1,"description":"olfactory receptor family 2 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8244]"}, {"versioned_ensembl_gene_id":"ENSG00000274764.5","gene_symbol":"PRAMEF27","gene_name":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101929983","summary":null,"start":13049476,"end":13056491,"strand":-1,"description":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]"}, {"versioned_ensembl_gene_id":"ENSG00000141404.15","gene_symbol":"GNAL","gene_name":"G protein subunit alpha L [Source:HGNC Symbol;Acc:HGNC:4388]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2774","summary":"This gene encodes a stimulatory G protein alpha subunit which mediates odorant signaling in the olfactory epithelium. This protein couples dopamine type 1 receptors and adenosine A2A receptors and is widely expressed in the central nervous system. Mutations in this gene have been associated with dystonia 25 and this gene is located in a susceptibility region for bipolar disorder and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":11688956,"end":11885685,"strand":1,"description":"G protein subunit alpha L [Source:HGNC Symbol;Acc:HGNC:4388]"}, {"versioned_ensembl_gene_id":"ENSG00000281521.1","gene_symbol":"AC116351.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1005039,"end":1006623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146540.14","gene_symbol":"C7orf50","gene_name":"chromosome 7 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:22421]","synonyms":"YCR016W,MGC11257","biotype":"protein_coding","ncbi_id":"84310","summary":null,"start":996986,"end":1138260,"strand":-1,"description":"chromosome 7 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:22421]"}, {"versioned_ensembl_gene_id":"ENSG00000253641.5","gene_symbol":"LINCR-0001","gene_name":"uncharacterized LINCR-0001 [Source:NCBI gene;Acc:101929191]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929191","summary":null,"start":10474565,"end":10481974,"strand":1,"description":"uncharacterized LINCR-0001 [Source:NCBI gene;Acc:101929191]"}, {"versioned_ensembl_gene_id":"ENSG00000226291.1","gene_symbol":"AC091729.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1080863,"end":1082178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226338.1","gene_symbol":"AC079150.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153208086,"end":153208163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168890.13","gene_symbol":"TMEM150A","gene_name":"transmembrane protein 150A [Source:HGNC Symbol;Acc:HGNC:24677]","synonyms":"TM6P1,FLJ90024,TTN1,TMEM150","biotype":"protein_coding","ncbi_id":"129303","summary":null,"start":85598548,"end":85603196,"strand":-1,"description":"transmembrane protein 150A [Source:HGNC Symbol;Acc:HGNC:24677]"}, {"versioned_ensembl_gene_id":"ENSG00000214025.2","gene_symbol":"ATP5F1P4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39745]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422514","summary":null,"start":153158938,"end":153159683,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39745]"}, {"versioned_ensembl_gene_id":"ENSG00000230889.2","gene_symbol":"SHC1P1","gene_name":"SHC adaptor protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10841]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"6465","summary":null,"start":64432401,"end":64434145,"strand":1,"description":"SHC adaptor protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10841]"}, {"versioned_ensembl_gene_id":"ENSG00000176236.6","gene_symbol":"C10orf111","gene_name":"chromosome 10 open reading frame 111 [Source:HGNC Symbol;Acc:HGNC:28582]","synonyms":"MGC35468,bA455B2.4","biotype":"bidirectional_promoter_lncRNA","ncbi_id":"221060","summary":null,"start":15095385,"end":15097319,"strand":-1,"description":"chromosome 10 open reading frame 111 [Source:HGNC Symbol;Acc:HGNC:28582]"}, {"versioned_ensembl_gene_id":"ENSG00000283349.2","gene_symbol":"AL034408.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64405473,"end":64406136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157219.3","gene_symbol":"HTR5A","gene_name":"5-hydroxytryptamine receptor 5A [Source:HGNC Symbol;Acc:HGNC:5300]","synonyms":"5-HT5A","biotype":"protein_coding","ncbi_id":"3361","summary":"The neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) has been implicated in a wide range of psychiatric conditions and also has vasoconstrictive and vasodilatory effects. The gene described in this record is a member of 5-hydroxytryptamine (serotonin) receptor family and encodes a multi-pass membrane protein that functions as a receptor for 5-hydroxytryptamine and couples to G-proteins. This protein has been shown to function in part through the regulation of intracellular Ca2+ mobilization. [provided by RefSeq, Jul 2008]","start":155070324,"end":155085749,"strand":1,"description":"5-hydroxytryptamine receptor 5A [Source:HGNC Symbol;Acc:HGNC:5300]"}, {"versioned_ensembl_gene_id":"ENSG00000234932.2","gene_symbol":"AC009969.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152850653,"end":152850824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248503.2","gene_symbol":"AL356235.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":77910741,"end":77964890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188124.3","gene_symbol":"OR2AG2","gene_name":"olfactory receptor family 2 subfamily AG member 2 [Source:HGNC Symbol;Acc:HGNC:15143]","synonyms":"OR2AG2P","biotype":"protein_coding","ncbi_id":"338755","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6765626,"end":6771976,"strand":-1,"description":"olfactory receptor family 2 subfamily AG member 2 [Source:HGNC Symbol;Acc:HGNC:15143]"}, {"versioned_ensembl_gene_id":"ENSG00000095739.10","gene_symbol":"BAMBI","gene_name":"BMP and activin membrane bound inhibitor [Source:HGNC Symbol;Acc:HGNC:30251]","synonyms":"NMA","biotype":"protein_coding","ncbi_id":"25805","summary":"This gene encodes a transmembrane glycoprotein related to the type I receptors of the transforming growth factor-beta (TGF-beta) family, whose members play important roles in signal transduction in many developmental and pathological processes. The encoded protein however is a pseudoreceptor, lacking an intracellular serine/threonine kinase domain required for signaling. Similar proteins in frog, mouse and zebrafish function as negative regulators of TGF-beta, which has led to the suggestion that the encoded protein may function to limit the signaling range of the TGF-beta family during early embryogenesis. [provided by RefSeq, Jul 2008]","start":28677342,"end":28682939,"strand":1,"description":"BMP and activin membrane bound inhibitor [Source:HGNC Symbol;Acc:HGNC:30251]"}, {"versioned_ensembl_gene_id":"ENSG00000280397.1","gene_symbol":"AC011592.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":144442211,"end":144445844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226273.2","gene_symbol":"AC079305.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177177695,"end":177178255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164535.14","gene_symbol":"DAGLB","gene_name":"diacylglycerol lipase beta [Source:HGNC Symbol;Acc:HGNC:28923]","synonyms":"KCCR13L,DAGLBETA","biotype":"protein_coding","ncbi_id":"221955","summary":null,"start":6409126,"end":6484190,"strand":-1,"description":"diacylglycerol lipase beta [Source:HGNC Symbol;Acc:HGNC:28923]"}, {"versioned_ensembl_gene_id":"ENSG00000166478.9","gene_symbol":"ZNF143","gene_name":"zinc finger protein 143 [Source:HGNC Symbol;Acc:HGNC:12928]","synonyms":"SBF,pHZ-1,STAF","biotype":"protein_coding","ncbi_id":"7702","summary":null,"start":9460319,"end":9528524,"strand":1,"description":"zinc finger protein 143 [Source:HGNC Symbol;Acc:HGNC:12928]"}, {"versioned_ensembl_gene_id":"ENSG00000061656.9","gene_symbol":"SPAG4","gene_name":"sperm associated antigen 4 [Source:HGNC Symbol;Acc:HGNC:11214]","synonyms":"SUN4,CT127","biotype":"protein_coding","ncbi_id":"6676","summary":"The mammalian sperm flagellum contains two cytoskeletal structures associated with the axoneme: the outer dense fibers surrounding the axoneme in the midpiece and principal piece and the fibrous sheath surrounding the outer dense fibers in the principal piece of the tail. Defects in these structures are associated with abnormal tail morphology, reduced sperm motility, and infertility. In the rat, the protein encoded by this gene associates with an outer dense fiber protein via a leucine zipper motif and localizes to the microtubules of the manchette and axoneme during sperm tail development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":35615892,"end":35621049,"strand":1,"description":"sperm associated antigen 4 [Source:HGNC Symbol;Acc:HGNC:11214]"}, {"versioned_ensembl_gene_id":"ENSG00000259589.2","gene_symbol":"AC073167.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63675146,"end":63713758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261655.1","gene_symbol":"AC100803.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":141353403,"end":141355365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260674.2","gene_symbol":"AC026826.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79743311,"end":79743468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273382.1","gene_symbol":"AL356488.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109087971,"end":109090858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267082.1","gene_symbol":"AC011472.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11203628,"end":11216168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102100.15","gene_symbol":"SLC35A2","gene_name":"solute carrier family 35 member A2 [Source:HGNC Symbol;Acc:HGNC:11022]","synonyms":"UGTL,UGT2,UGT1,UGT,UGAT,UGALT","biotype":"protein_coding","ncbi_id":"7355","summary":"This gene encodes a member of the nucleotide-sugar transporter family. The encoded protein is a multi-pass membrane protein. It transports UDP-galactose from the cytosol into Golgi vesicles, where it serves as a glycosyl donor for the generation of glycans. Mutations in this gene cause congenital disorder of glycosylation type IIm (CDG2M). Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":48903180,"end":48911958,"strand":-1,"description":"solute carrier family 35 member A2 [Source:HGNC Symbol;Acc:HGNC:11022]"}, {"versioned_ensembl_gene_id":"ENSG00000270491.1","gene_symbol":"AL359999.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34742906,"end":34743199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227372.11","gene_symbol":"TP73-AS1","gene_name":"TP73 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:29052]","synonyms":"PDAM,KIAA0495","biotype":"transcribed_unitary_pseudogene","ncbi_id":"57212","summary":null,"start":3735601,"end":3747336,"strand":-1,"description":"TP73 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:29052]"}, {"versioned_ensembl_gene_id":"ENSG00000236501.5","gene_symbol":"AC074286.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176990508,"end":177164516,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271369.1","gene_symbol":"AC087783.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34709600,"end":34710161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227589.1","gene_symbol":"AL136528.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3658938,"end":3668772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263916.1","gene_symbol":"AC100778.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49484536,"end":49486149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250726.1","gene_symbol":"AC107222.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184072403,"end":184073039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101365.20","gene_symbol":"IDH3B","gene_name":"isocitrate dehydrogenase 3 (NAD(+)) beta [Source:HGNC Symbol;Acc:HGNC:5385]","synonyms":"RP46","biotype":"protein_coding","ncbi_id":"3420","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. NAD(+)-dependent isocitrate dehydrogenases catalyze the allosterically regulated rate-limiting step of the tricarboxylic acid cycle. Each isozyme is a heterotetramer that is composed of two alpha subunits, one beta subunit, and one gamma subunit. The protein encoded by this gene is the beta subunit of one isozyme of NAD(+)-dependent isocitrate dehydrogenase. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Sep 2016]","start":2658395,"end":2664219,"strand":-1,"description":"isocitrate dehydrogenase 3 (NAD(+)) beta [Source:HGNC Symbol;Acc:HGNC:5385]"}, {"versioned_ensembl_gene_id":"ENSG00000232646.1","gene_symbol":"AL731563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73065126,"end":73065467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169189.16","gene_symbol":"NSMCE1","gene_name":"NSE1 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:29897]","synonyms":"NSE1","biotype":"protein_coding","ncbi_id":"197370","summary":null,"start":27224991,"end":27268794,"strand":-1,"description":"NSE1 homolog, SMC5-SMC6 complex component [Source:HGNC Symbol;Acc:HGNC:29897]"}, {"versioned_ensembl_gene_id":"ENSG00000237749.4","gene_symbol":"AL034379.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37556247,"end":37556499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283355.1","gene_symbol":"AC074194.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":184014035,"end":184016382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103599.19","gene_symbol":"IQCH","gene_name":"IQ motif containing H [Source:HGNC Symbol;Acc:HGNC:25721]","synonyms":"FLJ12476","biotype":"protein_coding","ncbi_id":"64799","summary":null,"start":67254800,"end":67502260,"strand":1,"description":"IQ motif containing H [Source:HGNC Symbol;Acc:HGNC:25721]"}, {"versioned_ensembl_gene_id":"ENSG00000232491.1","gene_symbol":"SAPCD2P3","gene_name":"suppressor APC domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51279]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643353","summary":null,"start":66556216,"end":66557065,"strand":1,"description":"suppressor APC domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51279]"}, {"versioned_ensembl_gene_id":"ENSG00000243531.1","gene_symbol":"AC079804.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6900424,"end":6900623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230039.1","gene_symbol":"AL450487.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65821255,"end":65822249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110880.10","gene_symbol":"CORO1C","gene_name":"coronin 1C [Source:HGNC Symbol;Acc:HGNC:2254]","synonyms":"HCRNN4,coronin-3","biotype":"protein_coding","ncbi_id":"23603","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]","start":108645109,"end":108731596,"strand":-1,"description":"coronin 1C [Source:HGNC Symbol;Acc:HGNC:2254]"}, {"versioned_ensembl_gene_id":"ENSG00000158109.14","gene_symbol":"TPRG1L","gene_name":"tumor protein p63 regulated 1 like [Source:HGNC Symbol;Acc:HGNC:27007]","synonyms":"FLJ21811,FAM79A,RP11-46F15.3","biotype":"protein_coding","ncbi_id":"127262","summary":null,"start":3625002,"end":3630127,"strand":1,"description":"tumor protein p63 regulated 1 like [Source:HGNC Symbol;Acc:HGNC:27007]"}, {"versioned_ensembl_gene_id":"ENSG00000277059.2","gene_symbol":"FAM30A","gene_name":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]","synonyms":"KIAA0125,HSPC053,C14orf110","biotype":"lincRNA","ncbi_id":"9834","summary":null,"start":105918750,"end":105933413,"strand":1,"description":"family with sequence similarity 30 member A [Source:HGNC Symbol;Acc:HGNC:19955]"}, {"versioned_ensembl_gene_id":"ENSG00000260552.1","gene_symbol":"AC023043.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36179996,"end":36187448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155666.11","gene_symbol":"KDM8","gene_name":"lysine demethylase 8 [Source:HGNC Symbol;Acc:HGNC:25840]","synonyms":"JMJD5,FLJ13798","biotype":"protein_coding","ncbi_id":"79831","summary":"This gene likely encodes a histone lysine demethylase. Studies of a similar protein in mouse indicate a potential role for this protein as a tumor suppressor. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2009]","start":27203495,"end":27221768,"strand":1,"description":"lysine demethylase 8 [Source:HGNC Symbol;Acc:HGNC:25840]"}, {"versioned_ensembl_gene_id":"ENSG00000078618.21","gene_symbol":"NRDC","gene_name":"nardilysin convertase [Source:HGNC Symbol;Acc:HGNC:7995]","synonyms":"NRD1,hNRD2,hNRD1","biotype":"protein_coding","ncbi_id":"4898","summary":"This gene encodes a zinc-dependent endopeptidase that cleaves peptide substrates at the N-terminus of arginine residues in dibasic moieties and is a member of the peptidase M16 family. This protein interacts with heparin-binding EGF-like growth factor and plays a role in cell migration and proliferation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":51789191,"end":51878937,"strand":-1,"description":"nardilysin convertase [Source:HGNC Symbol;Acc:HGNC:7995]"}, {"versioned_ensembl_gene_id":"ENSG00000205897.5","gene_symbol":"OR7E136P","gene_name":"olfactory receptor family 7 subfamily E member 136 pseudogene [Source:HGNC Symbol;Acc:HGNC:19557]","synonyms":"OR7E147P,OR7E139P","biotype":"unprocessed_pseudogene","ncbi_id":"155340","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6866658,"end":6867672,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 136 pseudogene [Source:HGNC Symbol;Acc:HGNC:19557]"}, {"versioned_ensembl_gene_id":"ENSG00000111641.11","gene_symbol":"NOP2","gene_name":"NOP2 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:7867]","synonyms":"NOP120,NOL1,p120,NSUN1","biotype":"protein_coding","ncbi_id":"4839","summary":null,"start":6556863,"end":6568691,"strand":-1,"description":"NOP2 nucleolar protein [Source:HGNC Symbol;Acc:HGNC:7867]"}, {"versioned_ensembl_gene_id":"ENSG00000236444.4","gene_symbol":"UBE2L5P","gene_name":"ubiquitin conjugating enzyme E2 L5, pseudogene [Source:HGNC Symbol;Acc:HGNC:13477]","synonyms":"UBE2L5","biotype":"protein_coding","ncbi_id":"171222","summary":null,"start":30422488,"end":30428616,"strand":1,"description":"ubiquitin conjugating enzyme E2 L5, pseudogene [Source:HGNC Symbol;Acc:HGNC:13477]"}, {"versioned_ensembl_gene_id":"ENSG00000233562.1","gene_symbol":"AL356981.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183266602,"end":183267285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270062.1","gene_symbol":"AL606834.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50723777,"end":50724272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135423.12","gene_symbol":"GLS2","gene_name":"glutaminase 2 [Source:HGNC Symbol;Acc:HGNC:29570]","synonyms":"LGA,hLGA,GLS,GA","biotype":"protein_coding","ncbi_id":"27165","summary":"The protein encoded by this gene is a mitochondrial phosphate-activated glutaminase that catalyzes the hydrolysis of glutamine to stoichiometric amounts of glutamate and ammonia. Originally thought to be liver-specific, this protein has been found in other tissues as well. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":56470944,"end":56488414,"strand":-1,"description":"glutaminase 2 [Source:HGNC Symbol;Acc:HGNC:29570]"}, {"versioned_ensembl_gene_id":"ENSG00000171823.6","gene_symbol":"FBXL14","gene_name":"F-box and leucine rich repeat protein 14 [Source:HGNC Symbol;Acc:HGNC:28624]","synonyms":"MGC40195,Fbl14","biotype":"protein_coding","ncbi_id":"144699","summary":"Members of the F-box protein family, such as FBXL14, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":1565993,"end":1594165,"strand":-1,"description":"F-box and leucine rich repeat protein 14 [Source:HGNC Symbol;Acc:HGNC:28624]"}, {"versioned_ensembl_gene_id":"ENSG00000235110.5","gene_symbol":"AC107421.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143855739,"end":143856142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179021.9","gene_symbol":"C3orf38","gene_name":"chromosome 3 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:28384]","synonyms":"MGC26717","biotype":"protein_coding","ncbi_id":"285237","summary":null,"start":88149743,"end":88168729,"strand":1,"description":"chromosome 3 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:28384]"}, {"versioned_ensembl_gene_id":"ENSG00000280193.1","gene_symbol":"AC132219.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81696368,"end":81698694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224577.1","gene_symbol":"LINC01117","gene_name":"long intergenic non-protein coding RNA 1117 [Source:HGNC Symbol;Acc:HGNC:49260]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724224","summary":null,"start":176637710,"end":176655958,"strand":1,"description":"long intergenic non-protein coding RNA 1117 [Source:HGNC Symbol;Acc:HGNC:49260]"}, {"versioned_ensembl_gene_id":"ENSG00000253598.1","gene_symbol":"SLC10A5","gene_name":"solute carrier family 10 member 5 [Source:HGNC Symbol;Acc:HGNC:22981]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347051","summary":null,"start":81693607,"end":81696174,"strand":-1,"description":"solute carrier family 10 member 5 [Source:HGNC Symbol;Acc:HGNC:22981]"}, {"versioned_ensembl_gene_id":"ENSG00000282132.1","gene_symbol":"IGHD2-8","gene_name":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]","synonyms":"IGHD28,DLR1","biotype":"IG_D_gene","ncbi_id":"28504","summary":null,"start":105907982,"end":105908012,"strand":-1,"description":"immunoglobulin heavy diversity 2-8 [Source:HGNC Symbol;Acc:HGNC:5492]"}, {"versioned_ensembl_gene_id":"ENSG00000206062.4","gene_symbol":"AL121823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91307781,"end":91308878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282373.1","gene_symbol":"IGHD3-10","gene_name":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]","synonyms":"IGHD310,DXP'1","biotype":"IG_D_gene","ncbi_id":"28499","summary":null,"start":105905268,"end":105905298,"strand":-1,"description":"immunoglobulin heavy diversity 3-10 [Source:HGNC Symbol;Acc:HGNC:5495]"}, {"versioned_ensembl_gene_id":"ENSG00000272800.1","gene_symbol":"AC021851.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183214319,"end":183215400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235988.1","gene_symbol":"AC245100.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148317683,"end":148318013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235281.1","gene_symbol":"AL713851.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2501783,"end":2567239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234694.1","gene_symbol":"AL139289.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43354684,"end":43358658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272824.1","gene_symbol":"AC245100.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148358245,"end":148358686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273252.1","gene_symbol":"AC079882.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6835420,"end":6835794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179097.5","gene_symbol":"HTR1F","gene_name":"5-hydroxytryptamine receptor 1F [Source:HGNC Symbol;Acc:HGNC:5292]","synonyms":"HTR1EL,5-HT1F","biotype":"protein_coding","ncbi_id":"3355","summary":null,"start":87990696,"end":87993835,"strand":1,"description":"5-hydroxytryptamine receptor 1F [Source:HGNC Symbol;Acc:HGNC:5292]"}, {"versioned_ensembl_gene_id":"ENSG00000238121.5","gene_symbol":"LINC00426","gene_name":"long intergenic non-protein coding RNA 426 [Source:HGNC Symbol;Acc:HGNC:42761]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100188949","summary":null,"start":30340270,"end":30377145,"strand":-1,"description":"long intergenic non-protein coding RNA 426 [Source:HGNC Symbol;Acc:HGNC:42761]"}, {"versioned_ensembl_gene_id":"ENSG00000187730.8","gene_symbol":"GABRD","gene_name":"gamma-aminobutyric acid type A receptor delta subunit [Source:HGNC Symbol;Acc:HGNC:4084]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2563","summary":"Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. The GABA-A receptor is generally pentameric and there are five types of subunits: alpha, beta, gamma, delta, and rho. This gene encodes the delta subunit. Mutations in this gene have been associated with susceptibility to generalized epilepsy with febrile seizures, type 5. Alternatively spliced transcript variants have been described for this gene, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":2019298,"end":2030758,"strand":1,"description":"gamma-aminobutyric acid type A receptor delta subunit [Source:HGNC Symbol;Acc:HGNC:4084]"}, {"versioned_ensembl_gene_id":"ENSG00000218027.2","gene_symbol":"AL512329.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1513698,"end":1515289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272862.1","gene_symbol":"AC106052.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41988741,"end":41989237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232026.1","gene_symbol":"AL731683.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32641404,"end":32642234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164743.4","gene_symbol":"C8orf48","gene_name":"chromosome 8 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:26345]","synonyms":"FLJ25402","biotype":"protein_coding","ncbi_id":"157773","summary":null,"start":13566843,"end":13568287,"strand":1,"description":"chromosome 8 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:26345]"}, {"versioned_ensembl_gene_id":"ENSG00000224793.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32654132,"end":32655069,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000230384.1","gene_symbol":"RPSAP25","gene_name":"ribosomal protein SA pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36405]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"129841","summary":null,"start":176242111,"end":176242993,"strand":1,"description":"ribosomal protein SA pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36405]"}, {"versioned_ensembl_gene_id":"ENSG00000281145.1","gene_symbol":"IGLV5-45","gene_name":"immunoglobulin lambda variable 5-45 [Source:HGNC Symbol;Acc:HGNC:5924]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28781","summary":null,"start":22375985,"end":22376504,"strand":1,"description":"immunoglobulin lambda variable 5-45 [Source:HGNC Symbol;Acc:HGNC:5924]"}, {"versioned_ensembl_gene_id":"ENSG00000204256.12","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"BRD2-IT1,FSRG1,NAT,D6S113E,KIAA9001,RING3","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":32968660,"end":32981505,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000270745.1","gene_symbol":"AL731768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88982215,"end":88982353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263756.1","gene_symbol":"AL645941.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32972065,"end":32972853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282544.1","gene_symbol":"AC243660.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28445158,"end":28447993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236708.1","gene_symbol":"AC073316.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3264032,"end":3302452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100227.17","gene_symbol":"POLDIP3","gene_name":"DNA polymerase delta interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23782]","synonyms":"KIAA1649,PDIP46","biotype":"protein_coding","ncbi_id":"84271","summary":"This gene encodes an RRM (RNA recognition motif)-containing protein that participates in the regulation of translation by recruiting ribosomal protein S6 kinase beta-1 to mRNAs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":42583721,"end":42614962,"strand":-1,"description":"DNA polymerase delta interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:23782]"}, {"versioned_ensembl_gene_id":"ENSG00000101546.12","gene_symbol":"RBFA","gene_name":"ribosome binding factor A (putative) [Source:HGNC Symbol;Acc:HGNC:26120]","synonyms":"HsT169,FLJ21172,C18orf22","biotype":"protein_coding","ncbi_id":"79863","summary":null,"start":80034358,"end":80046397,"strand":1,"description":"ribosome binding factor A (putative) [Source:HGNC Symbol;Acc:HGNC:26120]"}, {"versioned_ensembl_gene_id":"ENSG00000230317.1","gene_symbol":"LINC01284","gene_name":"long intergenic non-protein coding RNA 1284 [Source:HGNC Symbol;Acc:HGNC:50342]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926971","summary":null,"start":51095844,"end":51171400,"strand":-1,"description":"long intergenic non-protein coding RNA 1284 [Source:HGNC Symbol;Acc:HGNC:50342]"}, {"versioned_ensembl_gene_id":"ENSG00000231679.7","gene_symbol":"HLA-DRB3","gene_name":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]","synonyms":"HLA-DR3B,HLA-DR3B","biotype":"protein_coding","ncbi_id":"3125","summary":"HLA-DRB3 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020]","start":32444128,"end":32457245,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 3 [Source:HGNC Symbol;Acc:HGNC:4951]"}, {"versioned_ensembl_gene_id":"ENSG00000122545.18","gene_symbol":"SEPT7","gene_name":"septin 7 [Source:HGNC Symbol;Acc:HGNC:1717]","synonyms":"SEPT7A,CDC3,CDC10","biotype":"protein_coding","ncbi_id":"989","summary":"This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. [provided by RefSeq, Jul 2011]","start":35800932,"end":35907105,"strand":1,"description":"septin 7 [Source:HGNC Symbol;Acc:HGNC:1717]"}, {"versioned_ensembl_gene_id":"ENSG00000261126.7","gene_symbol":"RBFADN","gene_name":"RBFA downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48591]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506070","summary":null,"start":80046900,"end":80095482,"strand":1,"description":"RBFA downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48591]"}, {"versioned_ensembl_gene_id":"ENSG00000234962.5","gene_symbol":"LINC00700","gene_name":"long intergenic non-protein coding RNA 700 [Source:HGNC Symbol;Acc:HGNC:27422]","synonyms":null,"biotype":"lincRNA","ncbi_id":"282980","summary":null,"start":2005473,"end":2014348,"strand":-1,"description":"long intergenic non-protein coding RNA 700 [Source:HGNC Symbol;Acc:HGNC:27422]"}, {"versioned_ensembl_gene_id":"ENSG00000236405.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30363112,"end":30364280,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000259646.1","gene_symbol":"AC140725.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":101903154,"end":101903204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228760.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31678475,"end":31692158,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000228944.1","gene_symbol":"AC004485.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24196662,"end":24255719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228464.1","gene_symbol":"AC073614.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26345236,"end":26346242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243440.6","gene_symbol":"AF130351.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":14591930,"end":14658821,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144852.17","gene_symbol":"NR1I2","gene_name":"nuclear receptor subfamily 1 group I member 2 [Source:HGNC Symbol;Acc:HGNC:7968]","synonyms":"SXR,PXR,PAR2,ONR1,BXR","biotype":"protein_coding","ncbi_id":"8856","summary":"This gene product belongs to the nuclear receptor superfamily, members of which are transcription factors characterized by a ligand-binding domain and a DNA-binding domain. The encoded protein is a transcriptional regulator of the cytochrome P450 gene CYP3A4, binding to the response element of the CYP3A4 promoter as a heterodimer with the 9-cis retinoic acid receptor RXR. It is activated by a range of compounds that induce CYP3A4, including dexamethasone and rifampicin. Several alternatively spliced transcripts encoding different isoforms, some of which use non-AUG (CUG) translation initiation codon, have been described for this gene. Additional transcript variants exist, however, they have not been fully characterized. [provided by RefSeq, Jul 2008]","start":119780484,"end":119818485,"strand":1,"description":"nuclear receptor subfamily 1 group I member 2 [Source:HGNC Symbol;Acc:HGNC:7968]"}, {"versioned_ensembl_gene_id":"ENSG00000254514.1","gene_symbol":"AC103855.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45582525,"end":45583474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205696.4","gene_symbol":"ADARB2-AS1","gene_name":"ADARB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23299]","synonyms":"NCRNA00168,C10orf109,bA466B20.1","biotype":"antisense_RNA","ncbi_id":"642394","summary":null,"start":1526637,"end":1556984,"strand":1,"description":"ADARB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23299]"}, {"versioned_ensembl_gene_id":"ENSG00000230952.1","gene_symbol":"AC099344.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11357515,"end":11365636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282390.1","gene_symbol":"AL392083.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1290018,"end":1293002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187166.1","gene_symbol":"H1FNT","gene_name":"H1 histone family member N, testis specific [Source:HGNC Symbol;Acc:HGNC:24893]","synonyms":"HANP1,H1T2","biotype":"protein_coding","ncbi_id":"341567","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-independent histone that is a member of the histone H1 family. The related mouse gene encodes a testis specific protein that is required for spermatogenesis and male fertility. [provided by RefSeq, Oct 2015]","start":48328980,"end":48330279,"strand":1,"description":"H1 histone family member N, testis specific [Source:HGNC Symbol;Acc:HGNC:24893]"}, {"versioned_ensembl_gene_id":"ENSG00000225280.6","gene_symbol":"AL158013.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21397818,"end":21400391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272744.1","gene_symbol":"AC107214.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183516894,"end":183517527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241837.6","gene_symbol":"ATP5O","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit [Source:HGNC Symbol;Acc:HGNC:850]","synonyms":"OSCP,ATPO","biotype":"protein_coding","ncbi_id":"539","summary":"The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance. [provided by RefSeq, Jul 2008]","start":33903453,"end":33915980,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit [Source:HGNC Symbol;Acc:HGNC:850]"}, {"versioned_ensembl_gene_id":"ENSG00000271677.1","gene_symbol":"Z82195.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130545586,"end":130546474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276349.4","gene_symbol":"TBC1D3L","gene_name":"TBC1 domain family member 3L [Source:HGNC Symbol;Acc:HGNC:51246]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060376","summary":null,"start":37982250,"end":37993199,"strand":-1,"description":"TBC1 domain family member 3L [Source:HGNC Symbol;Acc:HGNC:51246]"}, {"versioned_ensembl_gene_id":"ENSG00000224054.1","gene_symbol":"AL022163.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44466691,"end":44468955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095596.11","gene_symbol":"CYP26A1","gene_name":"cytochrome P450 family 26 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2603]","synonyms":"CYP26,CP26,P450RAI1,P450RAI","biotype":"protein_coding","ncbi_id":"1592","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein acts on retinoids, including all-trans-retinoic acid (RA), with both 4-hydroxylation and 18-hydroxylation activities. This enzyme regulates the cellular level of retinoic acid which is involved in regulation of gene expression in both embryonic and adult tissues. Two alternatively spliced transcript variants of this gene, which encode the distinct isoforms, have been reported. [provided by RefSeq, Jul 2008]","start":93073475,"end":93077890,"strand":1,"description":"cytochrome P450 family 26 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2603]"}, {"versioned_ensembl_gene_id":"ENSG00000151612.15","gene_symbol":"ZNF827","gene_name":"zinc finger protein 827 [Source:HGNC Symbol;Acc:HGNC:27193]","synonyms":null,"biotype":"protein_coding","ncbi_id":"152485","summary":null,"start":145757627,"end":145938635,"strand":-1,"description":"zinc finger protein 827 [Source:HGNC Symbol;Acc:HGNC:27193]"}, {"versioned_ensembl_gene_id":"ENSG00000186141.8","gene_symbol":"POLR3C","gene_name":"RNA polymerase III subunit C [Source:HGNC Symbol;Acc:HGNC:30076]","synonyms":"RPC62,RPC3","biotype":"protein_coding","ncbi_id":"10623","summary":null,"start":145824088,"end":145842505,"strand":1,"description":"RNA polymerase III subunit C [Source:HGNC Symbol;Acc:HGNC:30076]"}, {"versioned_ensembl_gene_id":"ENSG00000237136.7","gene_symbol":"C4orf51","gene_name":"chromosome 4 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:37264]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646603","summary":null,"start":145680115,"end":145771032,"strand":1,"description":"chromosome 4 open reading frame 51 [Source:HGNC Symbol;Acc:HGNC:37264]"}, {"versioned_ensembl_gene_id":"ENSG00000282343.1","gene_symbol":"KCNQ1-AS1","gene_name":"KCNQ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42790]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338653","summary":null,"start":2840112,"end":2861539,"strand":-1,"description":"KCNQ1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42790]"}, {"versioned_ensembl_gene_id":"ENSG00000257016.1","gene_symbol":"SLC25A39P2","gene_name":"SLC25A39 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107126289","summary":null,"start":10551266,"end":10551535,"strand":-1,"description":"SLC25A39 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48936]"}, {"versioned_ensembl_gene_id":"ENSG00000156222.11","gene_symbol":"SLC28A1","gene_name":"solute carrier family 28 member 1 [Source:HGNC Symbol;Acc:HGNC:11001]","synonyms":"CNT1","biotype":"protein_coding","ncbi_id":"9154","summary":null,"start":84884654,"end":84945796,"strand":1,"description":"solute carrier family 28 member 1 [Source:HGNC Symbol;Acc:HGNC:11001]"}, {"versioned_ensembl_gene_id":"ENSG00000279607.1","gene_symbol":"AL358613.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93071972,"end":93073466,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128271.21","gene_symbol":"ADORA2A","gene_name":"adenosine A2a receptor [Source:HGNC Symbol;Acc:HGNC:263]","synonyms":"RDC8,ADORA2","biotype":"protein_coding","ncbi_id":"135","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor (GPCR) superfamily, which is subdivided into classes and subtypes. The receptors are seven-pass transmembrane proteins that respond to extracellular cues and activate intracellular signal transduction pathways. This protein, an adenosine receptor of A2A subtype, uses adenosine as the preferred endogenous agonist and preferentially interacts with the G(s) and G(olf) family of G proteins to increase intracellular cAMP levels. It plays an important role in many biological functions, such as cardiac rhythm and circulation, cerebral and renal blood flow, immune function, pain regulation, and sleep. It has been implicated in pathophysiological conditions such as inflammatory diseases and neurodegenerative disorders. Alternative splicing results in multiple transcript variants. A read-through transcript composed of the upstream SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1-like) and ADORA2A (adenosine A2a receptor) gene sequence has been identified, but it is thought to be non-coding. [provided by RefSeq, Jun 2013]","start":24417879,"end":24442360,"strand":1,"description":"adenosine A2a receptor [Source:HGNC Symbol;Acc:HGNC:263]"}, {"versioned_ensembl_gene_id":"ENSG00000233017.2","gene_symbol":"AL121832.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62427827,"end":62447621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259347.6","gene_symbol":"AC087482.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66984108,"end":67065268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235387.2","gene_symbol":"SPAAR","gene_name":"small regulatory polypeptide of amino acid response [Source:HGNC Symbol;Acc:HGNC:27244]","synonyms":"SPAR,LINC00961","biotype":"protein_coding","ncbi_id":"158376","summary":null,"start":35909483,"end":35937153,"strand":1,"description":"small regulatory polypeptide of amino acid response [Source:HGNC Symbol;Acc:HGNC:27244]"}, {"versioned_ensembl_gene_id":"ENSG00000125999.10","gene_symbol":"BPIFB1","gene_name":"BPI fold containing family B member 1 [Source:HGNC Symbol;Acc:HGNC:16108]","synonyms":"VEMSGP,MGC14597,LPLUNC1,dJ1187J4.1,C20orf114,bA49G10.6","biotype":"protein_coding","ncbi_id":"92747","summary":"The protein encoded by this gene may be involved in the innate immune response to bacterial exposure in the mouth, nasal cavities, and lungs. The encoded protein is secreted and is a member of the BPI/LBP/PLUNC protein superfamily. This gene is found with other members of the superfamily in a cluster on chromosome 20. [provided by RefSeq, Jul 2008]","start":33273480,"end":33309878,"strand":1,"description":"BPI fold containing family B member 1 [Source:HGNC Symbol;Acc:HGNC:16108]"}, {"versioned_ensembl_gene_id":"ENSG00000224189.6","gene_symbol":"HAGLR","gene_name":"HOXD antisense growth-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43755]","synonyms":"Mdgt,HOXD-AS1","biotype":"antisense_RNA","ncbi_id":"401022","summary":null,"start":176173195,"end":176188958,"strand":-1,"description":"HOXD antisense growth-associated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:43755]"}, {"versioned_ensembl_gene_id":"ENSG00000205334.2","gene_symbol":"LINC01460","gene_name":"long intergenic non-protein coding RNA 1460 [Source:HGNC Symbol;Acc:HGNC:50858]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129995","summary":null,"start":27705786,"end":27715732,"strand":-1,"description":"long intergenic non-protein coding RNA 1460 [Source:HGNC Symbol;Acc:HGNC:50858]"}, {"versioned_ensembl_gene_id":"ENSG00000224271.5","gene_symbol":"AL117329.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47631674,"end":47855600,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244716.3","gene_symbol":"BX679664.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108992282,"end":108992836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258880.1","gene_symbol":"BX248244.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31697661,"end":31708679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277355.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789806,"end":54800882,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000226961.3","gene_symbol":"AC099344.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11351627,"end":11352118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233156.1","gene_symbol":"HSFY8P","gene_name":"heat shock transcription factor, Y-linked 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:38792]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480723","summary":null,"start":26011435,"end":26012237,"strand":1,"description":"heat shock transcription factor, Y-linked 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:38792]"}, {"versioned_ensembl_gene_id":"ENSG00000267413.1","gene_symbol":"LINC01901","gene_name":"long intergenic non-protein coding RNA 1901 [Source:HGNC Symbol;Acc:HGNC:52720]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372080","summary":null,"start":39841174,"end":39924840,"strand":-1,"description":"long intergenic non-protein coding RNA 1901 [Source:HGNC Symbol;Acc:HGNC:52720]"}, {"versioned_ensembl_gene_id":"ENSG00000206342.12","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":31961552,"end":31971824,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000147437.9","gene_symbol":"GNRH1","gene_name":"gonadotropin releasing hormone 1 [Source:HGNC Symbol;Acc:HGNC:4419]","synonyms":"GNRH,LHRH,GRH","biotype":"protein_coding","ncbi_id":"2796","summary":"This gene encodes a preproprotein that is proteolytically processed to generate a peptide that is a member of the gonadotropin-releasing hormone (GnRH) family of peptides. Alternative splicing results in multiple transcript variants, at least one of which is secreted and then cleaved to generate gonadoliberin-1 and GnRH-associated peptide 1. Gonadoliberin-1 stimulates the release of luteinizing and follicle stimulating hormones, which are important for reproduction. Mutations in this gene are associated with hypogonadotropic hypogonadism. [provided by RefSeq, Nov 2015]","start":25419260,"end":25424654,"strand":-1,"description":"gonadotropin releasing hormone 1 [Source:HGNC Symbol;Acc:HGNC:4419]"}, {"versioned_ensembl_gene_id":"ENSG00000225740.1","gene_symbol":"ELOCP6","gene_name":"elongin C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38142]","synonyms":"TCEB1P6","biotype":"processed_pseudogene","ncbi_id":"100462867","summary":null,"start":17837201,"end":17837528,"strand":-1,"description":"elongin C pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38142]"}, {"versioned_ensembl_gene_id":"ENSG00000224964.1","gene_symbol":"TRAPPC2P3","gene_name":"trafficking protein particle complex 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10712]","synonyms":"SEDLP3","biotype":"unprocessed_pseudogene","ncbi_id":"27195","summary":null,"start":17797983,"end":17800696,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10712]"}, {"versioned_ensembl_gene_id":"ENSG00000282106.1","gene_symbol":"LINC00588","gene_name":"long intergenic non-protein coding RNA 588 [Source:HGNC Symbol;Acc:HGNC:24494]","synonyms":"DKFZP434F122,C8orf71","biotype":"lincRNA","ncbi_id":"26138","summary":null,"start":57291307,"end":57296495,"strand":1,"description":"long intergenic non-protein coding RNA 588 [Source:HGNC Symbol;Acc:HGNC:24494]"}, {"versioned_ensembl_gene_id":"ENSG00000235521.1","gene_symbol":"USP9YP27","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:38763]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480716","summary":null,"start":17788315,"end":17789484,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:38763]"}, {"versioned_ensembl_gene_id":"ENSG00000237205.1","gene_symbol":"RPL7P34","gene_name":"ribosomal protein L7 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36181]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389992","summary":null,"start":88618223,"end":88618934,"strand":-1,"description":"ribosomal protein L7 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36181]"}, {"versioned_ensembl_gene_id":"ENSG00000106565.17","gene_symbol":"TMEM176B","gene_name":"transmembrane protein 176B [Source:HGNC Symbol;Acc:HGNC:29596]","synonyms":"MS4B2,LR8","biotype":"protein_coding","ncbi_id":"28959","summary":null,"start":150791285,"end":150801360,"strand":-1,"description":"transmembrane protein 176B [Source:HGNC Symbol;Acc:HGNC:29596]"}, {"versioned_ensembl_gene_id":"ENSG00000224143.10","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"C6orf30,G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31872446,"end":31882289,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000229740.1","gene_symbol":"U91324.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8139402,"end":8143269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233659.1","gene_symbol":"NDUFA5P4","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48846]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128136","summary":null,"start":35874810,"end":35875194,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48846]"}, {"versioned_ensembl_gene_id":"ENSG00000233690.1","gene_symbol":"EBAG9P1","gene_name":"estrogen receptor binding site associated, antigen, 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45233]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422254","summary":null,"start":99697407,"end":99697949,"strand":-1,"description":"estrogen receptor binding site associated, antigen, 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45233]"}, {"versioned_ensembl_gene_id":"ENSG00000225287.1","gene_symbol":"OFD1P13Y","gene_name":"OFD1 pseudogene 13, Y-linked [Source:HGNC Symbol;Acc:HGNC:23885]","synonyms":"OFDYP13,OFD1PY13,OFD1P13","biotype":"unprocessed_pseudogene","ncbi_id":"386697","summary":null,"start":25675060,"end":25697346,"strand":-1,"description":"OFD1 pseudogene 13, Y-linked [Source:HGNC Symbol;Acc:HGNC:23885]"}, {"versioned_ensembl_gene_id":"ENSG00000272977.1","gene_symbol":"AL008721.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25476218,"end":25479971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229651.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30404972,"end":30409576,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000135898.9","gene_symbol":"GPR55","gene_name":"G protein-coupled receptor 55 [Source:HGNC Symbol;Acc:HGNC:4511]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9290","summary":"This gene belongs to the G-protein-coupled receptor superfamily. The encoded integral membrane protein is a likely cannabinoid receptor. It may be involved in several physiological and pathological processes by activating a variety of signal transduction pathways. [provided by RefSeq, Aug 2013]","start":230907318,"end":230961066,"strand":-1,"description":"G protein-coupled receptor 55 [Source:HGNC Symbol;Acc:HGNC:4511]"}, {"versioned_ensembl_gene_id":"ENSG00000056972.18","gene_symbol":"TRAF3IP2","gene_name":"TRAF3 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:1343]","synonyms":"DKFZP586G0522,CIKS,C6orf6,C6orf5,C6orf4,C6orf2,ACT1","biotype":"protein_coding","ncbi_id":"10758","summary":"This gene encodes a protein involved in regulating responses to cytokines by members of the Rel/NF-kappaB transcription factor family. These factors play a central role in innate immunity in response to pathogens, inflammatory signals and stress. This gene product interacts with TRAF proteins (tumor necrosis factor receptor-associated factors) and either I-kappaB kinase or MAP kinase to activate either NF-kappaB or Jun kinase. Several alternative transcripts encoding different isoforms have been identified. Another transcript, which does not encode a protein and is transcribed in the opposite orientation, has been identified. Overexpression of this transcript has been shown to reduce expression of at least one of the protein encoding transcripts, suggesting it has a regulatory role in the expression of this gene. [provided by RefSeq, Aug 2009]","start":111556454,"end":111606278,"strand":-1,"description":"TRAF3 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:1343]"}, {"versioned_ensembl_gene_id":"ENSG00000271815.1","gene_symbol":"AC008897.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75363760,"end":75364242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000056291.17","gene_symbol":"NPFFR2","gene_name":"neuropeptide FF receptor 2 [Source:HGNC Symbol;Acc:HGNC:4525]","synonyms":"NPGPR,NPFF2,GPR74","biotype":"protein_coding","ncbi_id":"10886","summary":"This gene encodes a member of a subfamily of G-protein-coupled neuropeptide receptors. This protein is activated by the neuropeptides A-18-amide (NPAF) and F-8-amide (NPFF) and may function in pain modulation and regulation of the opioid system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":72031804,"end":72148067,"strand":1,"description":"neuropeptide FF receptor 2 [Source:HGNC Symbol;Acc:HGNC:4525]"}, {"versioned_ensembl_gene_id":"ENSG00000183785.14","gene_symbol":"TUBA8","gene_name":"tubulin alpha 8 [Source:HGNC Symbol;Acc:HGNC:12410]","synonyms":"TUBAL2","biotype":"protein_coding","ncbi_id":"51807","summary":"This gene encodes a member of the alpha tubulin protein family. Alpha tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. Mutations in this gene are associated with polymicrogyria and optic nerve hypoplasia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]","start":18110331,"end":18146554,"strand":1,"description":"tubulin alpha 8 [Source:HGNC Symbol;Acc:HGNC:12410]"}, {"versioned_ensembl_gene_id":"ENSG00000280154.1","gene_symbol":"AC073255.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30408170,"end":30408346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196427.13","gene_symbol":"NBPF4","gene_name":"NBPF member 4 [Source:HGNC Symbol;Acc:HGNC:26550]","synonyms":"FLJ32833","biotype":"protein_coding","ncbi_id":"148545","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Mar 2013]","start":108223341,"end":108244081,"strand":-1,"description":"NBPF member 4 [Source:HGNC Symbol;Acc:HGNC:26550]"}, {"versioned_ensembl_gene_id":"ENSG00000280007.1","gene_symbol":"AC008079.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18110759,"end":18131154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198183.11","gene_symbol":"BPIFA1","gene_name":"BPI fold containing family A member 1 [Source:HGNC Symbol;Acc:HGNC:15749]","synonyms":"SPLUNC1,PLUNC,LUNX,bA49G10.5","biotype":"protein_coding","ncbi_id":"51297","summary":"This gene is the human homolog of murine plunc, and like the mouse gene, is specifically expressed in the upper airways and nasopharyngeal regions. The encoded antimicrobial protein displays antibacterial activity against Gram-negative bacteria. It is thought to be involved in inflammatory responses to irritants in the upper airways and may also serve as a potential molecular marker for detection of micrometastasis in non-small-cell lung cancer. Multiple transcript variants resulting from alternative splicing in the 3' UTR have been detected, but the full-length nature of only three are known. [provided by RefSeq, Aug 2014]","start":33235995,"end":33243311,"strand":1,"description":"BPI fold containing family A member 1 [Source:HGNC Symbol;Acc:HGNC:15749]"}, {"versioned_ensembl_gene_id":"ENSG00000236408.1","gene_symbol":"AC073336.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154838388,"end":154865483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270114.1","gene_symbol":"AC006019.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154026287,"end":154038604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281887.3","gene_symbol":"GIMAP1-GIMAP5","gene_name":"GIMAP1-GIMAP5 readthrough [Source:HGNC Symbol;Acc:HGNC:51257]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527949","summary":"This locus represents naturally occurring readthrough transcription between the neighboring GIMAP1 (GTPase, IMAP family member 1) and GIMAP5 (GTPase, IMAP family member 5) genes on chromosome 7. Alternative splicing results in multiple readthrough transcript variants, one of which encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jan 2015]","start":150716668,"end":150743646,"strand":1,"description":"GIMAP1-GIMAP5 readthrough [Source:HGNC Symbol;Acc:HGNC:51257]"}, {"versioned_ensembl_gene_id":"ENSG00000172288.7","gene_symbol":"CDY1","gene_name":"chromodomain Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:1809]","synonyms":"CDY1A","biotype":"protein_coding","ncbi_id":"9085","summary":"This gene encodes a protein containing a chromodomain and a histone acetyltransferase catalytic domain. Chromodomain proteins are components of heterochromatin-like complexes and can act as gene repressors. This protein is localized to the nucleus of late spermatids where histone hyperacetylation takes place. Histone hyperacetylation is thought to facilitate the transition in which protamines replace histones as the major DNA-packaging protein. The human chromosome Y has two identical copies of this gene within a palindromic region; this record represents the more telomeric copy. Chromosome Y also contains a pair of closely related genes in another more telomeric palindrome as well as several related pseudogenes. Two protein isoforms are encoded by transcript variants of this gene. Additional transcript variants have been described, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":25622162,"end":25624902,"strand":1,"description":"chromodomain Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:1809]"}, {"versioned_ensembl_gene_id":"ENSG00000100068.11","gene_symbol":"LRP5L","gene_name":"LDL receptor related protein 5 like [Source:HGNC Symbol;Acc:HGNC:25323]","synonyms":"DKFZp434O0213","biotype":"protein_coding","ncbi_id":"91355","summary":null,"start":25351418,"end":25405377,"strand":-1,"description":"LDL receptor related protein 5 like [Source:HGNC Symbol;Acc:HGNC:25323]"}, {"versioned_ensembl_gene_id":"ENSG00000259983.1","gene_symbol":"AC018845.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":47013957,"end":47014365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238192.1","gene_symbol":"BX284656.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48139461,"end":48141001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099817.11","gene_symbol":"POLR2E","gene_name":"RNA polymerase II subunit E [Source:HGNC Symbol;Acc:HGNC:9192]","synonyms":"XAP4,RPB5,RPABC1,hsRPB5,hRPB25","biotype":"protein_coding","ncbi_id":"5434","summary":"This gene encodes the fifth largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. This subunit is shared by the other two DNA-directed RNA polymerases and is present in two-fold molar excess over the other polymerase subunits. An interaction between this subunit and a hepatitis virus transactivating protein has been demonstrated, suggesting that interaction between transcriptional activators and the polymerase can occur through this subunit. A pseudogene is located on chromosome 11. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":1086579,"end":1095380,"strand":-1,"description":"RNA polymerase II subunit E [Source:HGNC Symbol;Acc:HGNC:9192]"}, {"versioned_ensembl_gene_id":"ENSG00000137806.8","gene_symbol":"NDUFAF1","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:18828]","synonyms":"CIA30,CGI-65","biotype":"protein_coding","ncbi_id":"51103","summary":"This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Dec 2011]","start":41387349,"end":41402519,"strand":-1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:18828]"}, {"versioned_ensembl_gene_id":"ENSG00000258384.1","gene_symbol":"AC068831.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90952239,"end":90955225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231298.6","gene_symbol":"LINC00704","gene_name":"long intergenic non-protein coding RNA 704 [Source:HGNC Symbol;Acc:HGNC:44678]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100216001","summary":null,"start":4650185,"end":4678154,"strand":-1,"description":"long intergenic non-protein coding RNA 704 [Source:HGNC Symbol;Acc:HGNC:44678]"}, {"versioned_ensembl_gene_id":"ENSG00000236681.1","gene_symbol":"DSTNP5","gene_name":"destrin, actin depolymerizing factor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44549]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132132","summary":null,"start":204306842,"end":204307364,"strand":1,"description":"destrin, actin depolymerizing factor pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44549]"}, {"versioned_ensembl_gene_id":"ENSG00000232064.1","gene_symbol":"USP9YP33","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:38777]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478931","summary":null,"start":25590323,"end":25592345,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:38777]"}, {"versioned_ensembl_gene_id":"ENSG00000258323.1","gene_symbol":"AC073575.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112063909,"end":112065755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128652.11","gene_symbol":"HOXD3","gene_name":"homeobox D3 [Source:HGNC Symbol;Acc:HGNC:5137]","synonyms":"HOX4A,HOX4,HOX1D","biotype":"protein_coding","ncbi_id":"3232","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The protein encoded by this gene may play a role in the regulation of cell adhesion processes. [provided by RefSeq, Jul 2008]","start":176136612,"end":176173102,"strand":1,"description":"homeobox D3 [Source:HGNC Symbol;Acc:HGNC:5137]"}, {"versioned_ensembl_gene_id":"ENSG00000270921.1","gene_symbol":"CICP23","gene_name":"capicua transcriptional repressor pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:48833]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505953","summary":null,"start":123312,"end":126123,"strand":1,"description":"capicua transcriptional repressor pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:48833]"}, {"versioned_ensembl_gene_id":"ENSG00000275272.4","gene_symbol":"YTHDC1","gene_name":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]","synonyms":"YT521-B,YT521,KIAA1966","biotype":"protein_coding","ncbi_id":"91746","summary":null,"start":68310387,"end":68350089,"strand":-1,"description":"YTH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30626]"}, {"versioned_ensembl_gene_id":"ENSG00000231889.7","gene_symbol":"TRAF3IP2-AS1","gene_name":"TRAF3IP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40005]","synonyms":"C6UAS,C6orf3,TRAF3IP2-AS2,NCRNA00248","biotype":"antisense_RNA","ncbi_id":"643749","summary":null,"start":111483511,"end":111598302,"strand":1,"description":"TRAF3IP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40005]"}, {"versioned_ensembl_gene_id":"ENSG00000175161.13","gene_symbol":"CADM2","gene_name":"cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:29849]","synonyms":"Necl-3,IGSF4D,SynCAM2,NECL3","biotype":"protein_coding","ncbi_id":"253559","summary":"This gene encodes a member of the synaptic cell adhesion molecule 1 (SynCAM) family which belongs to the immunoglobulin (Ig) superfamily. The encoded protein has three Ig-like domains and a cytosolic protein 4.1 binding site near the C-terminus. Proteins belonging to the protein 4.1 family crosslink spectrin and interact with other cytoskeletal proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":84958981,"end":86074429,"strand":1,"description":"cell adhesion molecule 2 [Source:HGNC Symbol;Acc:HGNC:29849]"}, {"versioned_ensembl_gene_id":"ENSG00000133561.15","gene_symbol":"GIMAP6","gene_name":"GTPase, IMAP family member 6 [Source:HGNC Symbol;Acc:HGNC:21918]","synonyms":"IAN6,FLJ22690","biotype":"protein_coding","ncbi_id":"474344","summary":"This gene encodes a member of the GTPases of immunity-associated proteins (GIMAP) family. GIMAP proteins contain GTP-binding and coiled-coil motifs, and may play roles in the regulation of cell survival. Decreased expression of this gene may play a role in non-small cell lung cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, which is found in a cluster with seven additional GIMAP genes on the long arm of chromosome 7. [provided by RefSeq, Sep 2011]","start":150625375,"end":150632648,"strand":-1,"description":"GTPase, IMAP family member 6 [Source:HGNC Symbol;Acc:HGNC:21918]"}, {"versioned_ensembl_gene_id":"ENSG00000183566.10","gene_symbol":"BPIFA4P","gene_name":"BPI fold containing family A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:20469]","synonyms":"BASE","biotype":"transcribed_unitary_pseudogene","ncbi_id":"317716","summary":null,"start":33193585,"end":33210462,"strand":1,"description":"BPI fold containing family A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:20469]"}, {"versioned_ensembl_gene_id":"ENSG00000271582.1","gene_symbol":"AC073111.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150484061,"end":150485135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151692.14","gene_symbol":"RNF144A","gene_name":"ring finger protein 144A [Source:HGNC Symbol;Acc:HGNC:20457]","synonyms":"RNF144,KIAA0161,hUIP4,UBCE7IP4","biotype":"protein_coding","ncbi_id":"9781","summary":"This gene encodes a member of a family of RING finger domain-containing E3 ubiquitin ligases that also includes parkin and parc. The expression of this gene is induced by DNA damage. The encoded protein interacts with the cytoplasmic DNA-dependent protein kinase, catalytic subunit (DNA-PKcs) and promotes its degradation through ubiquitination. The orthologous mouse protein has been shown to interact with a ubiquitin-conjugating enzyme involved in embryonic development. [provided by RefSeq, Mar 2017]","start":6917392,"end":7068286,"strand":1,"description":"ring finger protein 144A [Source:HGNC Symbol;Acc:HGNC:20457]"}, {"versioned_ensembl_gene_id":"ENSG00000276420.5","gene_symbol":"PRAMEF5","gene_name":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]","synonyms":"PRAMEF5L,PRAMEF23","biotype":"protein_coding","ncbi_id":"343068","summary":null,"start":13272778,"end":13282015,"strand":1,"description":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]"}, {"versioned_ensembl_gene_id":"ENSG00000215910.7","gene_symbol":"C1orf167","gene_name":"chromosome 1 open reading frame 167 [Source:HGNC Symbol;Acc:HGNC:25262]","synonyms":"RP11-56N19.2,DKFZp434E1410","biotype":"protein_coding","ncbi_id":"284498","summary":null,"start":11761787,"end":11789585,"strand":1,"description":"chromosome 1 open reading frame 167 [Source:HGNC Symbol;Acc:HGNC:25262]"}, {"versioned_ensembl_gene_id":"ENSG00000101040.19","gene_symbol":"ZMYND8","gene_name":"zinc finger MYND-type containing 8 [Source:HGNC Symbol;Acc:HGNC:9397]","synonyms":"RACK7,PRKCBP1","biotype":"protein_coding","ncbi_id":"23613","summary":"The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47209214,"end":47356889,"strand":-1,"description":"zinc finger MYND-type containing 8 [Source:HGNC Symbol;Acc:HGNC:9397]"}, {"versioned_ensembl_gene_id":"ENSG00000253840.1","gene_symbol":"AC044836.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54247633,"end":54247906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178567.7","gene_symbol":"EPM2AIP1","gene_name":"EPM2A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:19735]","synonyms":"KIAA0766,FLJ11207","biotype":"protein_coding","ncbi_id":"9852","summary":"The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]","start":36985043,"end":36993168,"strand":-1,"description":"EPM2A interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:19735]"}, {"versioned_ensembl_gene_id":"ENSG00000071282.11","gene_symbol":"LMCD1","gene_name":"LIM and cysteine rich domains 1 [Source:HGNC Symbol;Acc:HGNC:6633]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29995","summary":"This gene encodes a member of the LIM-domain family of zinc finger proteins. The encoded protein contains an N-terminal cysteine-rich domain and two C-terminal LIM domains. The presence of LIM domains suggests involvement in protein-protein interactions. The protein may act as a co-regulator of transcription along with other transcription factors. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":8501707,"end":8574673,"strand":1,"description":"LIM and cysteine rich domains 1 [Source:HGNC Symbol;Acc:HGNC:6633]"}, {"versioned_ensembl_gene_id":"ENSG00000227294.1","gene_symbol":"AC016994.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106834464,"end":106841207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104626.14","gene_symbol":"ERI1","gene_name":"exoribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:23994]","synonyms":"THEX1,3'HEXO","biotype":"protein_coding","ncbi_id":"90459","summary":null,"start":9002147,"end":9116746,"strand":1,"description":"exoribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:23994]"}, {"versioned_ensembl_gene_id":"ENSG00000122966.15","gene_symbol":"CIT","gene_name":"citron rho-interacting serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1985]","synonyms":"STK21,KIAA0949,CRIK,CITK","biotype":"protein_coding","ncbi_id":"11113","summary":"This gene encodes a serine/threonine-protein kinase that functions in cell division. Together with the kinesin KIF14, this protein localizes to the central spindle and midbody, and functions to promote efficient cytokinesis. This protein is involved in central nervous system development. Polymorphisms in this gene are associated with bipolar disorder and risk for schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":119685790,"end":119877291,"strand":-1,"description":"citron rho-interacting serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:1985]"}, {"versioned_ensembl_gene_id":"ENSG00000259396.1","gene_symbol":"AC087721.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41343080,"end":41344225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213403.2","gene_symbol":"CISD1P1","gene_name":"CDGSH iron sulfur domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29611]","synonyms":"ZCD1B,CISD1B","biotype":"processed_pseudogene","ncbi_id":"130500","summary":null,"start":19826249,"end":19826575,"strand":1,"description":"CDGSH iron sulfur domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29611]"}, {"versioned_ensembl_gene_id":"ENSG00000236665.1","gene_symbol":"AC114808.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1158310,"end":1160424,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125514.9","gene_symbol":"LINC00029","gene_name":"long intergenic non-protein coding RNA 29 [Source:HGNC Symbol;Acc:HGNC:16184]","synonyms":"NCRNA00029,C20orf51,bA305P22.4","biotype":"lincRNA","ncbi_id":"100144596","summary":null,"start":63034217,"end":63037028,"strand":-1,"description":"long intergenic non-protein coding RNA 29 [Source:HGNC Symbol;Acc:HGNC:16184]"}, {"versioned_ensembl_gene_id":"ENSG00000216708.1","gene_symbol":"CIR1P3","gene_name":"corepressor interacting with RBPJ, 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480783","summary":null,"start":34430880,"end":34431649,"strand":1,"description":"corepressor interacting with RBPJ, 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44013]"}, {"versioned_ensembl_gene_id":"ENSG00000250732.1","gene_symbol":"RPEP1","gene_name":"ribulose-5-phosphate-3-epimerase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44520]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420512","summary":null,"start":65251127,"end":65251784,"strand":-1,"description":"ribulose-5-phosphate-3-epimerase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44520]"}, {"versioned_ensembl_gene_id":"ENSG00000248288.1","gene_symbol":"AC008868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65209921,"end":65210948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254014.1","gene_symbol":"AC009902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81244156,"end":81244338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165338.16","gene_symbol":"HECTD2","gene_name":"HECT domain E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:26736]","synonyms":"FLJ37306","biotype":"protein_coding","ncbi_id":"143279","summary":null,"start":91409280,"end":91514829,"strand":1,"description":"HECT domain E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:26736]"}, {"versioned_ensembl_gene_id":"ENSG00000225366.4","gene_symbol":"TDGF1P3","gene_name":"teratocarcinoma-derived growth factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:11703]","synonyms":"TDGF3,TDGF2,CRIPTO3,CRIPTO-3,CR-3","biotype":"transcribed_processed_pseudogene","ncbi_id":"6998","summary":"The TDGF3 locus has characteristics of a retrotransposon, including lack of introns and a poly(A) sequence. [provided by RefSeq, Jul 2008]","start":110520312,"end":110523021,"strand":1,"description":"teratocarcinoma-derived growth factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:11703]"}, {"versioned_ensembl_gene_id":"ENSG00000232948.1","gene_symbol":"DEFB130A","gene_name":"defensin beta 130A [Source:HGNC Symbol;Acc:HGNC:18107]","synonyms":"DEFB30,DEFB130,DEFB-30","biotype":"protein_coding","ncbi_id":"245940","summary":"Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 8p23. [provided by RefSeq, Nov 2014]","start":12310962,"end":12318316,"strand":-1,"description":"defensin beta 130A [Source:HGNC Symbol;Acc:HGNC:18107]"}, {"versioned_ensembl_gene_id":"ENSG00000111846.16","gene_symbol":"GCNT2","gene_name":"glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) [Source:HGNC Symbol;Acc:HGNC:4204]","synonyms":"bA360O19.2,ULG3,NAGCT1,NACGT1,II,IGNT,GCNT5,CCAT,bA421M1.1","biotype":"protein_coding","ncbi_id":"2651","summary":"This gene encodes the enzyme responsible for formation of the blood group I antigen. The i and I antigens are distinguished by linear and branched poly-N-acetyllactosaminoglycans, respectively. The encoded protein is the I-branching enzyme, a beta-1,6-N-acetylglucosaminyltransferase responsible for the conversion of fetal i antigen to adult I antigen in erythrocytes during embryonic development. Mutations in this gene have been associated with adult i blood group phenotype. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":10492223,"end":10629368,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) [Source:HGNC Symbol;Acc:HGNC:4204]"}, {"versioned_ensembl_gene_id":"ENSG00000274947.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832654,"end":54848283,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000164970.14","gene_symbol":"FAM219A","gene_name":"family with sequence similarity 219 member A [Source:HGNC Symbol;Acc:HGNC:19920]","synonyms":"bA573M23.5,FLJ39031,C9orf25","biotype":"protein_coding","ncbi_id":"203259","summary":"The protein encoded by this gene has homologs that have been identified in mouse, macaque, etc organisms. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Dec 2010]","start":34398184,"end":34458570,"strand":-1,"description":"family with sequence similarity 219 member A [Source:HGNC Symbol;Acc:HGNC:19920]"}, {"versioned_ensembl_gene_id":"ENSG00000246016.2","gene_symbol":"LINC01513","gene_name":"long intergenic non-protein coding RNA 1513 [Source:HGNC Symbol;Acc:HGNC:51202]","synonyms":"TCONS_00009352,RP11-1C1.7","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10479371,"end":10482309,"strand":1,"description":"long intergenic non-protein coding RNA 1513 [Source:HGNC Symbol;Acc:HGNC:51202]"}, {"versioned_ensembl_gene_id":"ENSG00000273793.3","gene_symbol":"DUSP8","gene_name":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]","synonyms":"HB5,FLJ42958,C11orf81,HVH-5","biotype":"protein_coding","ncbi_id":"1850","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates SAPK/JNK and p38, is expressed predominantly in the adult brain, heart, and skeletal muscle, is localized in the cytoplasm, and is induced by nerve growth factor and insulin. An intronless pseudogene for DUSP8 is present on chromosome 10q11.2. [provided by RefSeq, Jul 2008]","start":1559754,"end":1577630,"strand":-1,"description":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]"}, {"versioned_ensembl_gene_id":"ENSG00000232298.2","gene_symbol":"AL138902.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24307556,"end":24321901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101665.8","gene_symbol":"SMAD7","gene_name":"SMAD family member 7 [Source:HGNC Symbol;Acc:HGNC:6773]","synonyms":"MADH8,MADH7","biotype":"protein_coding","ncbi_id":"4092","summary":"The protein encoded by this gene is a nuclear protein that binds the E3 ubiquitin ligase SMURF2. Upon binding, this complex translocates to the cytoplasm, where it interacts with TGF-beta receptor type-1 (TGFBR1), leading to the degradation of both the encoded protein and TGFBR1. Expression of this gene is induced by TGFBR1. Variations in this gene are a cause of susceptibility to colorectal cancer type 3 (CRCS3). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":48919853,"end":48950711,"strand":-1,"description":"SMAD family member 7 [Source:HGNC Symbol;Acc:HGNC:6773]"}, {"versioned_ensembl_gene_id":"ENSG00000224932.1","gene_symbol":"LINC02262","gene_name":"long intergenic non-protein coding RNA 2262 [Source:HGNC Symbol;Acc:HGNC:53174]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377389","summary":null,"start":117314597,"end":117360639,"strand":-1,"description":"long intergenic non-protein coding RNA 2262 [Source:HGNC Symbol;Acc:HGNC:53174]"}, {"versioned_ensembl_gene_id":"ENSG00000226054.2","gene_symbol":"MEMO1P1","gene_name":"mediator of cell motility 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23274]","synonyms":"MEMO1P,C21orf19","biotype":"processed_pseudogene","ncbi_id":"728556","summary":null,"start":36130489,"end":36131376,"strand":1,"description":"mediator of cell motility 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23274]"}, {"versioned_ensembl_gene_id":"ENSG00000166664.13","gene_symbol":"CHRFAM7A","gene_name":"CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion [Source:HGNC Symbol;Acc:HGNC:15781]","synonyms":"D-10,CHRNA7-DR1,D-10,CHRNA7-DR1","biotype":"protein_coding","ncbi_id":"89832","summary":"The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The family member CHRNA7, which is located on chromosome 15 in a region associated with several neuropsychiatric disorders, is partially duplicated and forms a hybrid with a novel gene from the family with sequence similarity 7 (FAM7A). Alternative splicing has been observed, and two variants exist, for this hybrid gene. The N-terminally truncated products predicted by the largest open reading frames for each variant would lack the majority of the neurotransmitter-gated ion-channel ligand binding domain but retain the transmembrane region that forms the ion channel. Although current evidence supports transcription of this hybrid gene, translation of the nicotinic acetylcholine receptor-like protein-encoding open reading frames has not been confirmed. [provided by RefSeq, Jul 2008]","start":30357766,"end":30393849,"strand":-1,"description":"CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion [Source:HGNC Symbol;Acc:HGNC:15781]"}, {"versioned_ensembl_gene_id":"ENSG00000226526.1","gene_symbol":"AL049569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16978926,"end":17005091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272235.1","gene_symbol":"AL590438.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3306636,"end":3310096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135108.14","gene_symbol":"FBXO21","gene_name":"F-box protein 21 [Source:HGNC Symbol;Acc:HGNC:13592]","synonyms":"KIAA0875,FBX21","biotype":"protein_coding","ncbi_id":"23014","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":117141988,"end":117190531,"strand":-1,"description":"F-box protein 21 [Source:HGNC Symbol;Acc:HGNC:13592]"}, {"versioned_ensembl_gene_id":"ENSG00000271053.1","gene_symbol":"AC093765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116858093,"end":116858973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100307.12","gene_symbol":"CBX7","gene_name":"chromobox 7 [Source:HGNC Symbol;Acc:HGNC:1557]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23492","summary":"This gene encodes a protein that contains the CHROMO (CHRomatin Organization MOdifier) domain. The encoded protein is a component of the Polycomb repressive complex 1 (PRC1), and is thought to control the lifespan of several normal human cells. [provided by RefSeq, Oct 2016]","start":39120167,"end":39152674,"strand":-1,"description":"chromobox 7 [Source:HGNC Symbol;Acc:HGNC:1557]"}, {"versioned_ensembl_gene_id":"ENSG00000250791.1","gene_symbol":"AC106892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116489364,"end":116515146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272121.1","gene_symbol":"AC006058.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43998081,"end":43999149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277594.2","gene_symbol":"DDX52","gene_name":"DExD-box helicase 52 [Source:HGNC Symbol;Acc:HGNC:20038]","synonyms":"ROK1","biotype":"protein_coding","ncbi_id":"11056","summary":null,"start":37614320,"end":37648026,"strand":-1,"description":"DExD-box helicase 52 [Source:HGNC Symbol;Acc:HGNC:20038]"}, {"versioned_ensembl_gene_id":"ENSG00000221977.2","gene_symbol":"OR4E2","gene_name":"olfactory receptor family 4 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:8297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26686","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21653835,"end":21667642,"strand":1,"description":"olfactory receptor family 4 subfamily E member 2 [Source:HGNC Symbol;Acc:HGNC:8297]"}, {"versioned_ensembl_gene_id":"ENSG00000267430.1","gene_symbol":"AC036176.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63415317,"end":63416469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230680.2","gene_symbol":"AC004869.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46477822,"end":46481578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229628.1","gene_symbol":"AC073115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45990905,"end":46000898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124209.3","gene_symbol":"RAB22A","gene_name":"RAB22A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9764]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57403","summary":"The protein encoded by this gene is a member of the RAB family of small GTPases. The GTP-bound form of the encoded protein has been shown to interact with early-endosomal antigen 1, and may be involved in the trafficking of and interaction between endosomal compartments. [provided by RefSeq, Jul 2008]","start":58309696,"end":58367507,"strand":1,"description":"RAB22A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9764]"}, {"versioned_ensembl_gene_id":"ENSG00000237471.1","gene_symbol":"AC073115.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45969657,"end":45980191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220132.1","gene_symbol":"AC236430.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49911620,"end":49912362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251359.4","gene_symbol":"WWC2-AS2","gene_name":"WWC2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:26390]","synonyms":"FLJ30277,C4orf38","biotype":"lincRNA","ncbi_id":"152641","summary":null,"start":183097017,"end":183099199,"strand":-1,"description":"WWC2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:26390]"}, {"versioned_ensembl_gene_id":"ENSG00000205916.11","gene_symbol":"DAZ4","gene_name":"deleted in azoospermia 4 [Source:HGNC Symbol;Acc:HGNC:15966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57135","summary":"This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains two copies of the 10.8 kb repeat. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Feb 2011]","start":24833843,"end":24907040,"strand":1,"description":"deleted in azoospermia 4 [Source:HGNC Symbol;Acc:HGNC:15966]"}, {"versioned_ensembl_gene_id":"ENSG00000153391.15","gene_symbol":"INO80C","gene_name":"INO80 complex subunit C [Source:HGNC Symbol;Acc:HGNC:26994]","synonyms":"IES6,hIes6,FLJ38183,C18orf37","biotype":"protein_coding","ncbi_id":"125476","summary":null,"start":35452230,"end":35497991,"strand":-1,"description":"INO80 complex subunit C [Source:HGNC Symbol;Acc:HGNC:26994]"}, {"versioned_ensembl_gene_id":"ENSG00000266401.1","gene_symbol":"AP002478.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3653410,"end":3656282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255644.1","gene_symbol":"AC010185.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21759980,"end":21766705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256734.1","gene_symbol":"AC027544.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18450112,"end":18450868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214207.2","gene_symbol":"KRT18P10","gene_name":"keratin 18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:23962]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360019","summary":null,"start":5573145,"end":5574431,"strand":1,"description":"keratin 18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:23962]"}, {"versioned_ensembl_gene_id":"ENSG00000196584.2","gene_symbol":"XRCC2","gene_name":"X-ray repair cross complementing 2 [Source:HGNC Symbol;Acc:HGNC:12829]","synonyms":"FANCU","biotype":"protein_coding","ncbi_id":"7516","summary":"This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double-strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents. [provided by RefSeq, Jul 2008]","start":152644779,"end":152676165,"strand":-1,"description":"X-ray repair cross complementing 2 [Source:HGNC Symbol;Acc:HGNC:12829]"}, {"versioned_ensembl_gene_id":"ENSG00000159459.11","gene_symbol":"UBR1","gene_name":"ubiquitin protein ligase E3 component n-recognin 1 [Source:HGNC Symbol;Acc:HGNC:16808]","synonyms":null,"biotype":"protein_coding","ncbi_id":"197131","summary":"The N-end rule pathway is one proteolytic pathway of the ubiquitin system. The recognition component of this pathway, encoded by this gene, binds to a destabilizing N-terminal residue of a substrate protein and participates in the formation of a substrate-linked multiubiquitin chain. This leads to the eventual degradation of the substrate protein. The protein described in this record has a RING-type zinc finger and a UBR-type zinc finger. Mutations in this gene have been associated with Johanson-Blizzard syndrome. [provided by RefSeq, Jul 2008]","start":42942897,"end":43106113,"strand":-1,"description":"ubiquitin protein ligase E3 component n-recognin 1 [Source:HGNC Symbol;Acc:HGNC:16808]"}, {"versioned_ensembl_gene_id":"ENSG00000232641.10","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTN6,BTNL11","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29656787,"end":29672153,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000227480.2","gene_symbol":"CCDC148-AS1","gene_name":"CCDC148 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44134]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"554201","summary":null,"start":158166650,"end":158236169,"strand":1,"description":"CCDC148 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44134]"}, {"versioned_ensembl_gene_id":"ENSG00000225720.6","gene_symbol":"AL031846.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39091586,"end":39092855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099785.10","gene_symbol":"MARCH2","gene_name":"membrane associated ring-CH-type finger 2 [Source:HGNC Symbol;Acc:HGNC:28038]","synonyms":"RNF172,MARCH-II,HSPC240","biotype":"protein_coding","ncbi_id":"51257","summary":"MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH2 reduces surface accumulation of several glycoproteins and appears to regulate early endosome-to-trans-Golgi network (TGN) trafficking (Bartee et al., 2004 [PubMed 14722266]; Nakamura et al., 2005 [PubMed 15689499]).[supplied by OMIM, Mar 2010]","start":8413270,"end":8439017,"strand":1,"description":"membrane associated ring-CH-type finger 2 [Source:HGNC Symbol;Acc:HGNC:28038]"}, {"versioned_ensembl_gene_id":"ENSG00000268931.1","gene_symbol":"AC136469.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8423355,"end":8427827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229153.5","gene_symbol":"EPHA1-AS1","gene_name":"EPHA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27799]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285965","summary":null,"start":143407813,"end":143523449,"strand":1,"description":"EPHA1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27799]"}, {"versioned_ensembl_gene_id":"ENSG00000234066.1","gene_symbol":"TAS2R62P","gene_name":"taste 2 receptor member 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:20640]","synonyms":"TAS2R62,T2R62","biotype":"unitary_pseudogene","ncbi_id":"338399","summary":null,"start":143437034,"end":143437973,"strand":1,"description":"taste 2 receptor member 62 pseudogene [Source:HGNC Symbol;Acc:HGNC:20640]"}, {"versioned_ensembl_gene_id":"ENSG00000112599.8","gene_symbol":"GUCA1B","gene_name":"guanylate cyclase activator 1B [Source:HGNC Symbol;Acc:HGNC:4679]","synonyms":"RP48,GCAP2","biotype":"protein_coding","ncbi_id":"2979","summary":"The protein encoded by this gene is a calcium-binding protein that activates photoreceptor guanylate cyclases. This gene may have arisen due to a gene duplication event since there is a highly similar gene clustered with it on chromosome 6. Mutations in this gene can cause a form of retinitis pigmentosa. [provided by RefSeq, Nov 2009]","start":42184401,"end":42194916,"strand":-1,"description":"guanylate cyclase activator 1B [Source:HGNC Symbol;Acc:HGNC:4679]"}, {"versioned_ensembl_gene_id":"ENSG00000237455.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32635116,"end":32635966,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000254875.8","gene_symbol":"AL845464.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32111446,"end":32129586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259725.1","gene_symbol":"AC106738.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54937786,"end":54938671,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259711.1","gene_symbol":"AC106738.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54934913,"end":54954665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254708.1","gene_symbol":"AL139174.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34335118,"end":34336003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259421.1","gene_symbol":"AL022318.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39070414,"end":39070671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143036.16","gene_symbol":"SLC44A3","gene_name":"solute carrier family 44 member 3 [Source:HGNC Symbol;Acc:HGNC:28689]","synonyms":"MGC45474,CTL3","biotype":"protein_coding","ncbi_id":"126969","summary":null,"start":94820342,"end":94895246,"strand":1,"description":"solute carrier family 44 member 3 [Source:HGNC Symbol;Acc:HGNC:28689]"}, {"versioned_ensembl_gene_id":"ENSG00000197644.2","gene_symbol":"AC106870.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29899597,"end":29907199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000094975.13","gene_symbol":"SUCO","gene_name":"SUN domain containing ossification factor [Source:HGNC Symbol;Acc:HGNC:1240]","synonyms":"SLP1,OPT,CH1,C1orf9","biotype":"protein_coding","ncbi_id":"51430","summary":null,"start":172532349,"end":172611833,"strand":1,"description":"SUN domain containing ossification factor [Source:HGNC Symbol;Acc:HGNC:1240]"}, {"versioned_ensembl_gene_id":"ENSG00000128607.13","gene_symbol":"KLHDC10","gene_name":"kelch domain containing 10 [Source:HGNC Symbol;Acc:HGNC:22194]","synonyms":"slim,KIAA0265","biotype":"protein_coding","ncbi_id":"23008","summary":null,"start":130070510,"end":130135720,"strand":1,"description":"kelch domain containing 10 [Source:HGNC Symbol;Acc:HGNC:22194]"}, {"versioned_ensembl_gene_id":"ENSG00000185507.19","gene_symbol":"IRF7","gene_name":"interferon regulatory factor 7 [Source:HGNC Symbol;Acc:HGNC:6122]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3665","summary":"IRF7 encodes interferon regulatory factor 7, a member of the interferon regulatory transcription factor (IRF) family. IRF7 has been shown to play a role in the transcriptional activation of virus-inducible cellular genes, including interferon beta chain genes. Inducible expression of IRF7 is largely restricted to lymphoid tissue. Multiple IRF7 transcript variants have been identified, although the functional consequences of these have not yet been established. [provided by RefSeq, Jul 2008]","start":612553,"end":615999,"strand":-1,"description":"interferon regulatory factor 7 [Source:HGNC Symbol;Acc:HGNC:6122]"}, {"versioned_ensembl_gene_id":"ENSG00000174099.10","gene_symbol":"MSRB3","gene_name":"methionine sulfoxide reductase B3 [Source:HGNC Symbol;Acc:HGNC:27375]","synonyms":"FLJ36866,DKFZp686C1178,DFNB74","biotype":"protein_coding","ncbi_id":"253827","summary":"The protein encoded by this gene catalyzes the reduction of methionine sulfoxide to methionine. This enzyme acts as a monomer and requires zinc as a cofactor. Several transcript variants encoding two different isoforms have been found for this gene. One of the isoforms localizes to mitochondria while the other localizes to endoplasmic reticula. [provided by RefSeq, Jul 2010]","start":65278643,"end":65488244,"strand":1,"description":"methionine sulfoxide reductase B3 [Source:HGNC Symbol;Acc:HGNC:27375]"}, {"versioned_ensembl_gene_id":"ENSG00000185594.4","gene_symbol":"SPATA8","gene_name":"spermatogenesis associated 8 [Source:HGNC Symbol;Acc:HGNC:28676]","synonyms":"MGC44294","biotype":"protein_coding","ncbi_id":"145946","summary":null,"start":96783389,"end":96785615,"strand":1,"description":"spermatogenesis associated 8 [Source:HGNC Symbol;Acc:HGNC:28676]"}, {"versioned_ensembl_gene_id":"ENSG00000222017.1","gene_symbol":"AC011997.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197693106,"end":197774823,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254405.10","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31727419,"end":31752228,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000282103.1","gene_symbol":"DLGAP2","gene_name":"DLG associated protein 2 [Source:NCBI gene;Acc:9228]","synonyms":"C8orf68,ERICH1-AS1,ERICH1-AS1,DAP2,DAP-2,C8orf68,SAPAP2","biotype":"antisense_RNA","ncbi_id":"9228","summary":"The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]","start":737651,"end":824587,"strand":1,"description":"DLG associated protein 2 [Source:NCBI gene;Acc:9228]"}, {"versioned_ensembl_gene_id":"ENSG00000117394.20","gene_symbol":"SLC2A1","gene_name":"solute carrier family 2 member 1 [Source:HGNC Symbol;Acc:HGNC:11005]","synonyms":"HTLVR,GLUT1,GLUT,DYT9,DYT18,CSE","biotype":"protein_coding","ncbi_id":"6513","summary":"This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]","start":42925375,"end":42959173,"strand":-1,"description":"solute carrier family 2 member 1 [Source:HGNC Symbol;Acc:HGNC:11005]"}, {"versioned_ensembl_gene_id":"ENSG00000282347.1","gene_symbol":"AC100797.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":725188,"end":725877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005339.14","gene_symbol":"CREBBP","gene_name":"CREB binding protein [Source:HGNC Symbol;Acc:HGNC:2348]","synonyms":"RTS,RSTS,KAT3A,CBP","biotype":"protein_coding","ncbi_id":"1387","summary":"This gene is ubiquitously expressed and is involved in the transcriptional coactivation of many different transcription factors. First isolated as a nuclear protein that binds to cAMP-response element binding protein (CREB), this gene is now known to play critical roles in embryonic development, growth control, and homeostasis by coupling chromatin remodeling to transcription factor recognition. The protein encoded by this gene has intrinsic histone acetyltransferase activity and also acts as a scaffold to stabilize additional protein interactions with the transcription complex. This protein acetylates both histone and non-histone proteins. This protein shares regions of very high sequence similarity with protein p300 in its bromodomain, cysteine-histidine-rich regions, and histone acetyltransferase domain. Mutations in this gene cause Rubinstein-Taybi syndrome (RTS). Chromosomal translocations involving this gene have been associated with acute myeloid leukemia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2009]","start":3725054,"end":3880726,"strand":-1,"description":"CREB binding protein [Source:HGNC Symbol;Acc:HGNC:2348]"}, {"versioned_ensembl_gene_id":"ENSG00000143258.15","gene_symbol":"USP21","gene_name":"ubiquitin specific peptidase 21 [Source:HGNC Symbol;Acc:HGNC:12620]","synonyms":"USP23,USP16","biotype":"protein_coding","ncbi_id":"27005","summary":"This gene encodes a member of the C19 peptidase family, also known as family 2 of ubiquitin carboxy-terminal hydrolases. The encoded protein cleaves ubiquitin from ubiquitinated proteins for recycling in intracellular protein degradation. The encoded protein is also able to release NEDD8, a ubiquitin-like protein, from NEDD8-conjugated proteins. This gene has been referred to as USP16 and USP23 but is now known as USP21. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":161159450,"end":161165723,"strand":1,"description":"ubiquitin specific peptidase 21 [Source:HGNC Symbol;Acc:HGNC:12620]"}, {"versioned_ensembl_gene_id":"ENSG00000233072.1","gene_symbol":"RPS15AP6","gene_name":"ribosomal protein S15a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35657]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271141","summary":null,"start":21003550,"end":21003934,"strand":-1,"description":"ribosomal protein S15a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35657]"}, {"versioned_ensembl_gene_id":"ENSG00000280844.1","gene_symbol":"KRT18P53","gene_name":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478925","summary":null,"start":547926,"end":548042,"strand":-1,"description":"keratin 18 pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:38714]"}, {"versioned_ensembl_gene_id":"ENSG00000264876.1","gene_symbol":"AP005209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10323132,"end":10372380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259876.1","gene_symbol":"AC010333.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12556353,"end":12557694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175604.2","gene_symbol":"AC007601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12086746,"end":12090302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278979.1","gene_symbol":"AC007598.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":12374355,"end":12376032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248738.6","gene_symbol":"AC037441.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22877972,"end":22888022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000048471.13","gene_symbol":"SNX29","gene_name":"sorting nexin 29 [Source:HGNC Symbol;Acc:HGNC:30542]","synonyms":"RUNDC2A,FLJ12363","biotype":"protein_coding","ncbi_id":"92017","summary":null,"start":11976737,"end":12574289,"strand":1,"description":"sorting nexin 29 [Source:HGNC Symbol;Acc:HGNC:30542]"}, {"versioned_ensembl_gene_id":"ENSG00000135318.11","gene_symbol":"NT5E","gene_name":"5'-nucleotidase ecto [Source:HGNC Symbol;Acc:HGNC:8021]","synonyms":"eNT,eN,CD73,CALJA,NT5","biotype":"protein_coding","ncbi_id":"4907","summary":"The protein encoded by this gene is a plasma membrane protein that catalyzes the conversion of extracellular nucleotides to membrane-permeable nucleosides. The encoded protein is used as a determinant of lymphocyte differentiation. Defects in this gene can lead to the calcification of joints and arteries. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]","start":85449584,"end":85495791,"strand":1,"description":"5'-nucleotidase ecto [Source:HGNC Symbol;Acc:HGNC:8021]"}, {"versioned_ensembl_gene_id":"ENSG00000280681.1","gene_symbol":"NEK4P1","gene_name":"NIMA-related kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39649]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421718","summary":null,"start":17210469,"end":17211347,"strand":-1,"description":"NIMA-related kinase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39649]"}, {"versioned_ensembl_gene_id":"ENSG00000214407.3","gene_symbol":"LINC02085","gene_name":"long intergenic non-protein coding RNA 2085 [Source:HGNC Symbol;Acc:HGNC:27190]","synonyms":null,"biotype":"lincRNA","ncbi_id":"152225","summary":null,"start":101940859,"end":101997926,"strand":1,"description":"long intergenic non-protein coding RNA 2085 [Source:HGNC Symbol;Acc:HGNC:27190]"}, {"versioned_ensembl_gene_id":"ENSG00000236418.8","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32606510,"end":32628863,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000156299.13","gene_symbol":"TIAM1","gene_name":"T-cell lymphoma invasion and metastasis 1 [Source:HGNC Symbol;Acc:HGNC:11805]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7074","summary":"This gene encodes a RAC1-specific guanine nucleotide exchange factor (GEF). GEFs mediate the exchange of guanosine diphosphate (GDP) for guanosine triphosphate (GTP). The binding of GTP induces a conformational change in RAC1 that allows downstream effectors to bind and transduce a signal. This gene thus regulates RAC1 signaling pathways that affect cell shape, migration, adhesion, growth, survival, and polarity, as well as influencing actin cytoskeletal formation, endocytosis, and membrane trafficking. This gene thus plays an important role in cell invasion, metastasis, and carcinogenesis. In addition to RAC1, the encoded protein activates additional Rho-like GTPases such as CDC42, RAC2, RAC3 and RHOA. This gene encodes multiple protein isoforms that experience a diverse array of intramolecular, protein-protein, and phosphorylation interactions as well as phosphoinositide binding. Both the longer and shorter isoforms have C-terminal Dbl homology (DH) and pleckstrin homology (PH) domains while only the longer isoforms of this gene have the N-terminal myristoylation site and the downstream N-terminal PH domain, ras-binding domain (RBD), and PSD-95/DlgA/ZO-1 (PDZ) domain. [provided by RefSeq, Jul 2017]","start":31118416,"end":31559977,"strand":-1,"description":"T-cell lymphoma invasion and metastasis 1 [Source:HGNC Symbol;Acc:HGNC:11805]"}, {"versioned_ensembl_gene_id":"ENSG00000260734.4","gene_symbol":"AC010547.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71430262,"end":71433376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137992.14","gene_symbol":"DBT","gene_name":"dihydrolipoamide branched chain transacylase E2 [Source:HGNC Symbol;Acc:HGNC:2698]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1629","summary":"The branched-chain alpha-keto acid dehydrogenase complex (BCKD) is an inner-mitochondrial enzyme complex involved in the breakdown of the branched-chain amino acids isoleucine, leucine, and valine. The BCKD complex is thought to be composed of a core of 24 transacylase (E2) subunits, and associated decarboxylase (E1), dehydrogenase (E3), and regulatory subunits. This gene encodes the transacylase (E2) subunit. Mutations in this gene result in maple syrup urine disease, type 2. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":100186919,"end":100249834,"strand":-1,"description":"dihydrolipoamide branched chain transacylase E2 [Source:HGNC Symbol;Acc:HGNC:2698]"}, {"versioned_ensembl_gene_id":"ENSG00000137394.14","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30141481,"end":30150469,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000105642.15","gene_symbol":"KCNN1","gene_name":"potassium calcium-activated channel subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:6290]","synonyms":"KCa2.1,hSK1","biotype":"protein_coding","ncbi_id":"3780","summary":"Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. This gene is a member of the KCNN family of potassium channel genes. [provided by RefSeq, Jul 2008]","start":17951293,"end":18000080,"strand":1,"description":"potassium calcium-activated channel subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:6290]"}, {"versioned_ensembl_gene_id":"ENSG00000227195.10","gene_symbol":"MIR663AHG","gene_name":"MIR663A host gene [Source:HGNC Symbol;Acc:HGNC:27662]","synonyms":"RP3-410C9.1","biotype":"processed_transcript","ncbi_id":"284801","summary":null,"start":26186920,"end":26251526,"strand":-1,"description":"MIR663A host gene [Source:HGNC Symbol;Acc:HGNC:27662]"}, {"versioned_ensembl_gene_id":"ENSG00000136696.10","gene_symbol":"IL36B","gene_name":"interleukin 36, beta [Source:HGNC Symbol;Acc:HGNC:15564]","synonyms":"MGC126882,MGC126880,IL1H2,IL1F8,IL1-ETA,IL-1H2,IL-1F8,FILI-(ETA),FIL1","biotype":"protein_coding","ncbi_id":"27177","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. Protein structure modeling indicated that this cytokine may contain a 12-stranded beta-trefoil structure that is conserved between IL1A (IL-A alpha) and IL1B (IL-1 beta). This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. Two alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":113022091,"end":113052867,"strand":-1,"description":"interleukin 36, beta [Source:HGNC Symbol;Acc:HGNC:15564]"}, {"versioned_ensembl_gene_id":"ENSG00000165874.12","gene_symbol":"FAM35BP","gene_name":"family with sequence similarity 35 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31425]","synonyms":"FAM35B,bA38L15.1,FAM35EP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"414241","summary":null,"start":46610474,"end":46652025,"strand":-1,"description":"family with sequence similarity 35 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31425]"}, {"versioned_ensembl_gene_id":"ENSG00000125780.11","gene_symbol":"TGM3","gene_name":"transglutaminase 3 [Source:HGNC Symbol;Acc:HGNC:11779]","synonyms":"TGE","biotype":"protein_coding","ncbi_id":"7053","summary":"Transglutaminases are enzymes that catalyze the crosslinking of proteins by epsilon-gamma glutamyl lysine isopeptide bonds. While the primary structure of transglutaminases is not conserved, they all have the same amino acid sequence at their active sites and their activity is calcium-dependent. The protein encoded by this gene consists of two polypeptide chains activated from a single precursor protein by proteolysis. The encoded protein is involved the later stages of cell envelope formation in the epidermis and hair follicle. [provided by RefSeq, Jul 2008]","start":2296001,"end":2341078,"strand":1,"description":"transglutaminase 3 [Source:HGNC Symbol;Acc:HGNC:11779]"}, {"versioned_ensembl_gene_id":"ENSG00000243402.1","gene_symbol":"AC022973.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129864478,"end":129865052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277559.1","gene_symbol":"AC018553.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54290965,"end":54292422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256164.1","gene_symbol":"CCND2-AS1","gene_name":"CCND2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49398]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103752584","summary":null,"start":4248765,"end":4276184,"strand":-1,"description":"CCND2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49398]"}, {"versioned_ensembl_gene_id":"ENSG00000274143.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5,CD158F,KIR2DL5.1,CD158F,KIR2DL5.1,KIR2DL5","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54476583,"end":54485924,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000277921.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000262594.4","gene_symbol":"KRTAP9-9","gene_name":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]","synonyms":"KRTAP9-5,KAP9.9,KAP9.5,KRTAP9-5,KAP9.9,KAP9.5","biotype":"protein_coding","ncbi_id":"81870","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. Alternative haplotypes of this gene are represented in the GRCh38 reference genome assembly. [provided by RefSeq, Dec 2015]","start":41244014,"end":41244994,"strand":1,"description":"keratin associated protein 9-9 [Source:HGNC Symbol;Acc:HGNC:16773]"}, {"versioned_ensembl_gene_id":"ENSG00000230888.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"dJ271M21,SMT3H2P,SUMO2P,SMT3Bp","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29635855,"end":29636138,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000269482.1","gene_symbol":"Z69720.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90631,"end":91102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236124.1","gene_symbol":"HMGN2P23","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39388]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874469","summary":null,"start":112981166,"end":112981434,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39388]"}, {"versioned_ensembl_gene_id":"ENSG00000168071.21","gene_symbol":"CCDC88B","gene_name":"coiled-coil domain containing 88B [Source:HGNC Symbol;Acc:HGNC:26757]","synonyms":"CCDC88,BRLZ,HkRP3,GIPIE,FLJ37970,FLJ00354","biotype":"protein_coding","ncbi_id":"283234","summary":"This gene encodes a member of the hook-related protein family. Members of this family are characterized by an N-terminal potential microtubule binding domain, a central coiled-coiled and a C-terminal Hook-related domain. The encoded protein may be involved in linking organelles to microtubules. [provided by RefSeq, Oct 2009]","start":64340223,"end":64357534,"strand":1,"description":"coiled-coil domain containing 88B [Source:HGNC Symbol;Acc:HGNC:26757]"}, {"versioned_ensembl_gene_id":"ENSG00000241220.1","gene_symbol":"AC078788.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153357107,"end":153374186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260367.2","gene_symbol":"AC109460.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28973962,"end":28978824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249170.1","gene_symbol":"AC096713.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71300258,"end":71301235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274372.4","gene_symbol":"AC239803.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148021850,"end":148025931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273059.1","gene_symbol":"AC239803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148011799,"end":148012228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215859.9","gene_symbol":"PDZK1P1","gene_name":"PDZ domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31974]","synonyms":"PDZK1P2,OTTHUMT00000038524,OTTHUMG00000074107","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100034743","summary":null,"start":147993862,"end":148014956,"strand":-1,"description":"PDZ domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31974]"}, {"versioned_ensembl_gene_id":"ENSG00000237282.3","gene_symbol":"LINC00851","gene_name":"long intergenic non-protein coding RNA 851 [Source:HGNC Symbol;Acc:HGNC:43424]","synonyms":"DZANK1-AS1","biotype":"antisense_RNA","ncbi_id":"440757","summary":null,"start":18379049,"end":18381484,"strand":1,"description":"long intergenic non-protein coding RNA 851 [Source:HGNC Symbol;Acc:HGNC:43424]"}, {"versioned_ensembl_gene_id":"ENSG00000169860.6","gene_symbol":"P2RY1","gene_name":"purinergic receptor P2Y1 [Source:HGNC Symbol;Acc:HGNC:8539]","synonyms":"P2Y1","biotype":"protein_coding","ncbi_id":"5028","summary":"The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor functions as a receptor for extracellular ATP and ADP. In platelets binding to ADP leads to mobilization of intracellular calcium ions via activation of phospholipase C, a change in platelet shape, and probably to platelet aggregation. [provided by RefSeq, Jul 2008]","start":152834693,"end":152841439,"strand":1,"description":"purinergic receptor P2Y1 [Source:HGNC Symbol;Acc:HGNC:8539]"}, {"versioned_ensembl_gene_id":"ENSG00000242561.1","gene_symbol":"ATP5LP5","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287091","summary":null,"start":152800434,"end":152800732,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38167]"}, {"versioned_ensembl_gene_id":"ENSG00000153989.7","gene_symbol":"NUS1","gene_name":"NUS1 dehydrodolichyl diphosphate synthase subunit [Source:HGNC Symbol;Acc:HGNC:21042]","synonyms":"C6orf68,TANGO14,NgBR,MGC7199","biotype":"protein_coding","ncbi_id":"116150","summary":"This gene encodes a type I single transmembrane domain receptor, which is a subunit of cis-prenyltransferase, and serves as a specific receptor for the neural and cardiovascular regulator Nogo-B. The encoded protein is essential for dolichol synthesis and protein glycosylation. This gene is highly expressed in non-small cell lung carcinomas as well as estrogen receptor-alpha positive breast cancer cells where it promotes epithelial mesenchymal transition. This gene is associated with the poor prognosis of human hepatocellular carcinoma patients. Naturally occurring mutations in this gene cause a congenital disorder of glycosylation and are associated with epilepsy. A knockout of the orthologous gene in mice causes embryonic lethality before day 6.5. Pseudogenes of this gene have been defined on chromosomes 13 and X. [provided by RefSeq, May 2017]","start":117675502,"end":117710640,"strand":1,"description":"NUS1 dehydrodolichyl diphosphate synthase subunit [Source:HGNC Symbol;Acc:HGNC:21042]"}, {"versioned_ensembl_gene_id":"ENSG00000218233.1","gene_symbol":"NEPNP","gene_name":"nephrocan, pseudogene [Source:HGNC Symbol;Acc:HGNC:33184]","synonyms":"NPN,NEPN","biotype":"unitary_pseudogene","ncbi_id":"442253","summary":"Nephrocan is a secreted glycoprotein that acts as an inhibitor of the transforming growth factor-beta signaling pathway. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, May 2010]","start":117633706,"end":117645087,"strand":1,"description":"nephrocan, pseudogene [Source:HGNC Symbol;Acc:HGNC:33184]"}, {"versioned_ensembl_gene_id":"ENSG00000282255.1","gene_symbol":"AC243742.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":15768444,"end":15769724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272784.1","gene_symbol":"AC019193.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183094423,"end":183095056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275211.4","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CPD6,P450C2D,CYP2D8P2,CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP","biotype":"protein_coding","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126495,"end":42130902,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000188338.14","gene_symbol":"SLC38A3","gene_name":"solute carrier family 38 member 3 [Source:HGNC Symbol;Acc:HGNC:18044]","synonyms":"SN1,G17","biotype":"protein_coding","ncbi_id":"10991","summary":null,"start":50205246,"end":50221486,"strand":1,"description":"solute carrier family 38 member 3 [Source:HGNC Symbol;Acc:HGNC:18044]"}, {"versioned_ensembl_gene_id":"ENSG00000230341.8","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"phostensin,KIAA1949","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30740303,"end":30751809,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000231068.1","gene_symbol":"KRTAP21-3","gene_name":"keratin associated protein 21-3 [Source:HGNC Symbol;Acc:HGNC:34216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288323","summary":null,"start":30718525,"end":30718777,"strand":-1,"description":"keratin associated protein 21-3 [Source:HGNC Symbol;Acc:HGNC:34216]"}, {"versioned_ensembl_gene_id":"ENSG00000250828.2","gene_symbol":"AC108078.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69437357,"end":69441050,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256103.2","gene_symbol":"ATP5J2P5","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654484","summary":null,"start":6270168,"end":6270425,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33611]"}, {"versioned_ensembl_gene_id":"ENSG00000227837.1","gene_symbol":"TRIM60P11Y","gene_name":"tripartite motif containing 60 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:38463]","synonyms":"TRIM60P11,TRIM60PY11","biotype":"processed_pseudogene","ncbi_id":"100420377","summary":null,"start":24691791,"end":24692932,"strand":1,"description":"tripartite motif containing 60 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:38463]"}, {"versioned_ensembl_gene_id":"ENSG00000231108.2","gene_symbol":"PRELID3BP11","gene_name":"PRELI domain containing 3B pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49073]","synonyms":"SLMO2P11","biotype":"processed_pseudogene","ncbi_id":"102723314","summary":null,"start":6734598,"end":6735076,"strand":-1,"description":"PRELI domain containing 3B pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49073]"}, {"versioned_ensembl_gene_id":"ENSG00000184724.5","gene_symbol":"KRTAP6-1","gene_name":"keratin associated protein 6-1 [Source:HGNC Symbol;Acc:HGNC:18931]","synonyms":"KAP6.1,C21orf103","biotype":"protein_coding","ncbi_id":"337966","summary":null,"start":30613431,"end":30613930,"strand":-1,"description":"keratin associated protein 6-1 [Source:HGNC Symbol;Acc:HGNC:18931]"}, {"versioned_ensembl_gene_id":"ENSG00000117528.11","gene_symbol":"ABCD3","gene_name":"ATP binding cassette subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:67]","synonyms":"ZWS2,PXMP1,PMP70","biotype":"protein_coding","ncbi_id":"5825","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":94418455,"end":94518666,"strand":1,"description":"ATP binding cassette subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:67]"}, {"versioned_ensembl_gene_id":"ENSG00000123415.15","gene_symbol":"SMUG1","gene_name":"single-strand-selective monofunctional uracil-DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:17148]","synonyms":"UNG3,HMUDG,FDG","biotype":"protein_coding","ncbi_id":"23583","summary":"This gene encodes a protein that participates in base excision repair by removing uracil from single- and double-stranded DNA. Many alternatively spliced transcript variants exist for this gene; the full-length nature is known for some but not all of the variants. [provided by RefSeq, Aug 2011]","start":54121277,"end":54189008,"strand":-1,"description":"single-strand-selective monofunctional uracil-DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:17148]"}, {"versioned_ensembl_gene_id":"ENSG00000240107.1","gene_symbol":"AC046144.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103538635,"end":103540487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247134.6","gene_symbol":"AC090204.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32996178,"end":33044855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249798.1","gene_symbol":"HSD3BP3","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:5221]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441900","summary":null,"start":119538509,"end":119545913,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:5221]"}, {"versioned_ensembl_gene_id":"ENSG00000250103.2","gene_symbol":"PANCR","gene_name":"PITX2 adjacent non-coding RNA [Source:HGNC Symbol;Acc:HGNC:52282]","synonyms":null,"biotype":"lincRNA","ncbi_id":"110231149","summary":null,"start":110595513,"end":110615458,"strand":-1,"description":"PITX2 adjacent non-coding RNA [Source:HGNC Symbol;Acc:HGNC:52282]"}, {"versioned_ensembl_gene_id":"ENSG00000272084.1","gene_symbol":"AL137127.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":19072110,"end":19075511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216439.1","gene_symbol":"DUTP5","gene_name":"deoxyuridine triphosphatase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873911","summary":null,"start":85426657,"end":85427125,"strand":-1,"description":"deoxyuridine triphosphatase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39518]"}, {"versioned_ensembl_gene_id":"ENSG00000185305.10","gene_symbol":"ARL15","gene_name":"ADP ribosylation factor like GTPase 15 [Source:HGNC Symbol;Acc:HGNC:25945]","synonyms":"FLJ20051,ARFRP2","biotype":"protein_coding","ncbi_id":"54622","summary":null,"start":53883945,"end":54310582,"strand":-1,"description":"ADP ribosylation factor like GTPase 15 [Source:HGNC Symbol;Acc:HGNC:25945]"}, {"versioned_ensembl_gene_id":"ENSG00000229570.2","gene_symbol":"GAPDHP58","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:4142]","synonyms":"GAPDL1,GAPDHL1","biotype":"processed_pseudogene","ncbi_id":"391077","summary":null,"start":119495836,"end":119496841,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:4142]"}, {"versioned_ensembl_gene_id":"ENSG00000273721.1","gene_symbol":"AC087385.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60409234,"end":60409420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242667.1","gene_symbol":"AC087385.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60404463,"end":60404960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281909.1","gene_symbol":"AC100757.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22480439,"end":22484840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257644.1","gene_symbol":"CR383656.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18631388,"end":18650966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230356.1","gene_symbol":"NCAPD2P1","gene_name":"non-SMC condensin I complex subunit D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421175","summary":null,"start":34750253,"end":34752053,"strand":-1,"description":"non-SMC condensin I complex subunit D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43831]"}, {"versioned_ensembl_gene_id":"ENSG00000230385.1","gene_symbol":"AC012507.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230908852,"end":230910102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137962.12","gene_symbol":"ARHGAP29","gene_name":"Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:HGNC:30207]","synonyms":"PARG1","biotype":"protein_coding","ncbi_id":"9411","summary":"Rap1 is a small GTPase that, through effectors, regulates Rho GTPase signaling. These effectors- Rasip1, Radil, and the protein encoded by this gene- translocate to the cell membrane, where they form a multiprotein complex. This complex is necessary for Rap1-induced inhibition of Rho signaling. Defects in this gene may be a cause of nonsyndromic cleft lip with or without cleft palate. [provided by RefSeq, Jun 2016]","start":94148988,"end":94275068,"strand":-1,"description":"Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:HGNC:30207]"}, {"versioned_ensembl_gene_id":"ENSG00000257175.2","gene_symbol":"CR383656.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18634955,"end":18637208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253596.1","gene_symbol":"AC103952.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74347757,"end":74350050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249360.1","gene_symbol":"AC034232.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33502072,"end":33503135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237158.1","gene_symbol":"AL353718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6568844,"end":6569360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237649.7","gene_symbol":"KIFC1","gene_name":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]","synonyms":"KNSL2,HSET","biotype":"protein_coding","ncbi_id":"3833","summary":null,"start":33391536,"end":33409924,"strand":1,"description":"kinesin family member C1 [Source:HGNC Symbol;Acc:HGNC:6389]"}, {"versioned_ensembl_gene_id":"ENSG00000204194.1","gene_symbol":"RPL12P1","gene_name":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]","synonyms":"RPL12-L,dJ570F3.5,CICK0721Q.1","biotype":"processed_pseudogene","ncbi_id":"729727","summary":null,"start":33400059,"end":33400556,"strand":-1,"description":"ribosomal protein L12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13976]"}, {"versioned_ensembl_gene_id":"ENSG00000275286.1","gene_symbol":"AC025253.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44498616,"end":44499158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227884.1","gene_symbol":"C4B-AS1","gene_name":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480730","summary":null,"start":31921995,"end":31929270,"strand":-1,"description":"C4B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39752]"}, {"versioned_ensembl_gene_id":"ENSG00000258315.5","gene_symbol":"C17orf49","gene_name":"chromosome 17 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28737]","synonyms":"MGC49942,HEPIS,BAP18","biotype":"protein_coding","ncbi_id":"124944","summary":null,"start":7014495,"end":7017525,"strand":1,"description":"chromosome 17 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:28737]"}, {"versioned_ensembl_gene_id":"ENSG00000225282.1","gene_symbol":"AP000350.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23926900,"end":23929574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273295.1","gene_symbol":"AP000350.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23901432,"end":23907068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277409.1","gene_symbol":"MAMDC2-AS1","gene_name":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507244","summary":null,"start":70087297,"end":70113866,"strand":-1,"description":"MAMDC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48719]"}, {"versioned_ensembl_gene_id":"ENSG00000140829.11","gene_symbol":"DHX38","gene_name":"DEAH-box helicase 38 [Source:HGNC Symbol;Acc:HGNC:17211]","synonyms":"PRPF16,PRP16,KIAA0224,hPrp16,DDX38","biotype":"protein_coding","ncbi_id":"9785","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a member of the DEAD/H box family of splicing factors. This protein resembles yeast Prp16 more closely than other DEAD/H family members. It is an ATPase and essential for the catalytic step II in pre-mRNA splicing process. [provided by RefSeq, Jul 2008]","start":72093562,"end":72112912,"strand":1,"description":"DEAH-box helicase 38 [Source:HGNC Symbol;Acc:HGNC:17211]"}, {"versioned_ensembl_gene_id":"ENSG00000261807.2","gene_symbol":"LINC02141","gene_name":"long intergenic non-protein coding RNA 2141 [Source:HGNC Symbol;Acc:HGNC:53001]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927580","summary":null,"start":59855353,"end":60053973,"strand":1,"description":"long intergenic non-protein coding RNA 2141 [Source:HGNC Symbol;Acc:HGNC:53001]"}, {"versioned_ensembl_gene_id":"ENSG00000166128.12","gene_symbol":"RAB8B","gene_name":"RAB8B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30273]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51762","summary":"RAB proteins, like RAB8B, are low molecular mass monomeric GTPases that localize on the cytoplasmic surfaces of distinct membrane-bound organelles. RAB proteins function in intracellular vesicle transport by aiding in the docking and/or fusion of vesicles with their target membranes (summary by Chen et al., 1997 [PubMed 9030196]).[supplied by OMIM, Nov 2010]","start":63189469,"end":63267782,"strand":1,"description":"RAB8B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:30273]"}, {"versioned_ensembl_gene_id":"ENSG00000117114.19","gene_symbol":"ADGRL2","gene_name":"adhesion G protein-coupled receptor L2 [Source:HGNC Symbol;Acc:HGNC:18582]","synonyms":"LPHH1,LEC1,KIAA0786,LPHN2","biotype":"protein_coding","ncbi_id":"23266","summary":"This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors. The encoded protein participates in the regulation of exocytosis. The proprotein is thought to be further cleaved within a cysteine-rich G-protein-coupled receptor proteolysis site into two chains that are non-covalently bound at the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":81306160,"end":81992436,"strand":1,"description":"adhesion G protein-coupled receptor L2 [Source:HGNC Symbol;Acc:HGNC:18582]"}, {"versioned_ensembl_gene_id":"ENSG00000280444.1","gene_symbol":"AC073592.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124623391,"end":124623987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273396.1","gene_symbol":"LINC01396","gene_name":"long intergenic non-protein coding RNA 1396 [Source:HGNC Symbol;Acc:HGNC:50675]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103695434","summary":null,"start":4844437,"end":4850827,"strand":1,"description":"long intergenic non-protein coding RNA 1396 [Source:HGNC Symbol;Acc:HGNC:50675]"}, {"versioned_ensembl_gene_id":"ENSG00000257721.1","gene_symbol":"CR383656.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18560047,"end":18560191,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261009.1","gene_symbol":"AC141257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33370473,"end":33372915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107295.9","gene_symbol":"SH3GL2","gene_name":"SH3 domain containing GRB2 like 2, endophilin A1 [Source:HGNC Symbol;Acc:HGNC:10831]","synonyms":"SH3P4,SH3D2A,EEN-B1,CNSA2","biotype":"protein_coding","ncbi_id":"6456","summary":null,"start":17579082,"end":17797129,"strand":1,"description":"SH3 domain containing GRB2 like 2, endophilin A1 [Source:HGNC Symbol;Acc:HGNC:10831]"}, {"versioned_ensembl_gene_id":"ENSG00000275113.1","gene_symbol":"GAGE2E","gene_name":"G antigen 2E [Source:HGNC Symbol;Acc:HGNC:31960]","synonyms":"GAGE8","biotype":"protein_coding","ncbi_id":"26749","summary":null,"start":49341192,"end":49345922,"strand":1,"description":"G antigen 2E [Source:HGNC Symbol;Acc:HGNC:31960]"}, {"versioned_ensembl_gene_id":"ENSG00000225886.3","gene_symbol":"AL445490.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27669468,"end":27703063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126709.14","gene_symbol":"IFI6","gene_name":"interferon alpha inducible protein 6 [Source:HGNC Symbol;Acc:HGNC:4054]","synonyms":"IFI616,IFI-6-16,G1P3,FAM14C,6-16","biotype":"protein_coding","ncbi_id":"2537","summary":"This gene was first identified as one of the many genes induced by interferon. The encoded protein may play a critical role in the regulation of apoptosis. A minisatellite that consists of 26 repeats of a 12 nucleotide repeating element resembling the mammalian splice donor consensus sequence begins near the end of the second exon. Alternatively spliced transcript variants that encode different isoforms by using the two downstream repeat units as splice donor sites have been described. [provided by RefSeq, Jul 2008]","start":27666061,"end":27672218,"strand":-1,"description":"interferon alpha inducible protein 6 [Source:HGNC Symbol;Acc:HGNC:4054]"}, {"versioned_ensembl_gene_id":"ENSG00000163286.8","gene_symbol":"ALPPL2","gene_name":"alkaline phosphatase, placental like 2 [Source:HGNC Symbol;Acc:HGNC:441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"251","summary":"There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The product of this gene is a membrane bound glycosylated enzyme, localized to testis, thymus and certain germ cell tumors, that is closely related to both the placental and intestinal forms of alkaline phosphatase. [provided by RefSeq, Jul 2008]","start":232406843,"end":232410714,"strand":1,"description":"alkaline phosphatase, placental like 2 [Source:HGNC Symbol;Acc:HGNC:441]"}, {"versioned_ensembl_gene_id":"ENSG00000235013.1","gene_symbol":"COX20P2","gene_name":"COX20, cytochrome c oxidase assembly factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289170","summary":null,"start":230957593,"end":230957950,"strand":1,"description":"COX20, cytochrome c oxidase assembly factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43772]"}, {"versioned_ensembl_gene_id":"ENSG00000283164.1","gene_symbol":"AC012507.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230924567,"end":230929919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231382.1","gene_symbol":"NBPF21P","gene_name":"NBPF member 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32001]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"205655","summary":"This pseudogene on chromosome 3 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Jun 2013]","start":36616006,"end":36637457,"strand":-1,"description":"NBPF member 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32001]"}, {"versioned_ensembl_gene_id":"ENSG00000225644.1","gene_symbol":"RPL35AP4","gene_name":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]","synonyms":"BPG294E21.7,OTTHUMG00000140156","biotype":"processed_pseudogene","ncbi_id":"100048922","summary":null,"start":33389374,"end":33389475,"strand":-1,"description":"ribosomal protein L35a pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33460]"}, {"versioned_ensembl_gene_id":"ENSG00000128266.8","gene_symbol":"GNAZ","gene_name":"G protein subunit alpha z [Source:HGNC Symbol;Acc:HGNC:4395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2781","summary":"The protein encoded by this gene is a member of a G protein subfamily that mediates signal transduction in pertussis toxin-insensitive systms. This encoded protein may play a role in maintaining the ionic balance of perilymphatic and endolymphatic cochlear fluids. [provided by RefSeq, Jul 2008]","start":23070361,"end":23125037,"strand":1,"description":"G protein subunit alpha z [Source:HGNC Symbol;Acc:HGNC:4395]"}, {"versioned_ensembl_gene_id":"ENSG00000137337.14","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"KIAA0170,Em:AB023051.5,NFBD1","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30699807,"end":30717889,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000163798.13","gene_symbol":"SLC4A1AP","gene_name":"solute carrier family 4 member 1 adaptor protein [Source:HGNC Symbol;Acc:HGNC:13813]","synonyms":"kanadaptin,HLC3","biotype":"protein_coding","ncbi_id":"22950","summary":null,"start":27663471,"end":27694976,"strand":1,"description":"solute carrier family 4 member 1 adaptor protein [Source:HGNC Symbol;Acc:HGNC:13813]"}, {"versioned_ensembl_gene_id":"ENSG00000219604.1","gene_symbol":"AL590143.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84689292,"end":84689429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228290.6","gene_symbol":"TBX18-AS1","gene_name":"TBX18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52256]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724201","summary":null,"start":84687712,"end":84709578,"strand":1,"description":"TBX18 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52256]"}, {"versioned_ensembl_gene_id":"ENSG00000100218.11","gene_symbol":"RSPH14","gene_name":"radial spoke head 14 homolog [Source:HGNC Symbol;Acc:HGNC:13437]","synonyms":"RTDR1","biotype":"protein_coding","ncbi_id":"27156","summary":"This gene encodes a protein with no known function but with slight similarity to a yeast vacuolar protein. The gene is located in a region deleted in pediatric rhabdoid tumors of the brain, kidney and soft tissues, but mutations in this gene have not been associated with the disease. [provided by RefSeq, Jul 2008]","start":23059415,"end":23145021,"strand":-1,"description":"radial spoke head 14 homolog [Source:HGNC Symbol;Acc:HGNC:13437]"}, {"versioned_ensembl_gene_id":"ENSG00000102103.15","gene_symbol":"PQBP1","gene_name":"polyglutamine binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9330]","synonyms":"MRX55,MRX2,SHS,RENS1,MRXS8,MRXS3","biotype":"protein_coding","ncbi_id":"10084","summary":"This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked cognitive disability. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009]","start":48897912,"end":48903143,"strand":1,"description":"polyglutamine binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9330]"}, {"versioned_ensembl_gene_id":"ENSG00000138095.18","gene_symbol":"LRPPRC","gene_name":"leucine rich pentatricopeptide repeat containing [Source:HGNC Symbol;Acc:HGNC:15714]","synonyms":"GP130,LSFC,LRP130","biotype":"protein_coding","ncbi_id":"10128","summary":"This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome. [provided by RefSeq, Mar 2012]","start":43886508,"end":43996005,"strand":-1,"description":"leucine rich pentatricopeptide repeat containing [Source:HGNC Symbol;Acc:HGNC:15714]"}, {"versioned_ensembl_gene_id":"ENSG00000228810.1","gene_symbol":"PABPC1P11","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37993]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421058","summary":null,"start":17589161,"end":17591318,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37993]"}, {"versioned_ensembl_gene_id":"ENSG00000180370.10","gene_symbol":"PAK2","gene_name":"p21 (RAC1) activated kinase 2 [Source:HGNC Symbol;Acc:HGNC:8591]","synonyms":"PAKgamma,PAK65","biotype":"protein_coding","ncbi_id":"5062","summary":"The p21 activated kinases (PAK) are critical effectors that link Rho GTPases to cytoskeleton reorganization and nuclear signaling. The PAK proteins are a family of serine/threonine kinases that serve as targets for the small GTP binding proteins, CDC42 and RAC1, and have been implicated in a wide range of biological activities. The protein encoded by this gene is activated by proteolytic cleavage during caspase-mediated apoptosis, and may play a role in regulating the apoptotic events in the dying cell. [provided by RefSeq, Jul 2008]","start":196739857,"end":196832647,"strand":1,"description":"p21 (RAC1) activated kinase 2 [Source:HGNC Symbol;Acc:HGNC:8591]"}, {"versioned_ensembl_gene_id":"ENSG00000271437.1","gene_symbol":"AL356423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98553243,"end":98553780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276672.1","gene_symbol":"AL161891.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33846190,"end":33850825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139797.7","gene_symbol":"RNF113B","gene_name":"ring finger protein 113B [Source:HGNC Symbol;Acc:HGNC:17267]","synonyms":"ZNF183L1,RNF161","biotype":"protein_coding","ncbi_id":"140432","summary":null,"start":98175785,"end":98177265,"strand":-1,"description":"ring finger protein 113B [Source:HGNC Symbol;Acc:HGNC:17267]"}, {"versioned_ensembl_gene_id":"ENSG00000133119.12","gene_symbol":"RFC3","gene_name":"replication factor C subunit 3 [Source:HGNC Symbol;Acc:HGNC:9971]","synonyms":"RFC38,MGC5276","biotype":"protein_coding","ncbi_id":"5983","summary":"The elongation of primed DNA templates by DNA polymerase delta and DNA polymerase epsilon requires the accessory proteins proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). RFC, also named activator 1, is a protein complex consisting of five distinct subunits of 140, 40, 38, 37, and 36 kDa. This gene encodes the 38 kDa subunit. This subunit is essential for the interaction between the 140 kDa subunit and the core complex that consists of the 36, 37, and 40 kDa subunits. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":33818049,"end":33966558,"strand":1,"description":"replication factor C subunit 3 [Source:HGNC Symbol;Acc:HGNC:9971]"}, {"versioned_ensembl_gene_id":"ENSG00000122386.10","gene_symbol":"ZNF205","gene_name":"zinc finger protein 205 [Source:HGNC Symbol;Acc:HGNC:12996]","synonyms":"ZNF210,Zfp13","biotype":"protein_coding","ncbi_id":"7755","summary":null,"start":3112560,"end":3120517,"strand":1,"description":"zinc finger protein 205 [Source:HGNC Symbol;Acc:HGNC:12996]"}, {"versioned_ensembl_gene_id":"ENSG00000198431.15","gene_symbol":"TXNRD1","gene_name":"thioredoxin reductase 1 [Source:HGNC Symbol;Acc:HGNC:12437]","synonyms":"TXNR,Trxr1,GRIM-12","biotype":"protein_coding","ncbi_id":"7296","summary":"The protein encoded by this gene belongs to the pyridine nucleotide-disulfide oxidoreductase family, and is a member of the thioredoxin (Trx) system. Three thioredoxin reductase (TrxR) isozymes are found in mammals. TrxRs are selenocysteine-containing flavoenzymes, which reduce thioredoxins, as well as other substrates, and play a key role in redox homoeostasis. This gene encodes an ubiquitously expressed, cytosolic form of TrxR, which functions as a homodimer containing FAD, and selenocysteine (Sec) at the active site. Sec is encoded by UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Alternative splicing, primarily at the 5' end, results in transcript variants encoding same or different isoforms, including a glutaredoxin-containing isoform that is predominantly expressed in testis. [provided by RefSeq, May 2017]","start":104215779,"end":104350305,"strand":1,"description":"thioredoxin reductase 1 [Source:HGNC Symbol;Acc:HGNC:12437]"}, {"versioned_ensembl_gene_id":"ENSG00000180917.17","gene_symbol":"CMTR2","gene_name":"cap methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:25635]","synonyms":"FTSJD1,FLJ11171,AFT,MTr2,FTSJD1,FLJ11171,AFT,MTr2","biotype":"protein_coding","ncbi_id":"55783","summary":null,"start":71281389,"end":71289715,"strand":-1,"description":"cap methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:25635]"}, {"versioned_ensembl_gene_id":"ENSG00000100867.14","gene_symbol":"DHRS2","gene_name":"dehydrogenase/reductase 2 [Source:HGNC Symbol;Acc:HGNC:18349]","synonyms":"SDR25C1,HEP27","biotype":"protein_coding","ncbi_id":"10202","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family, which has over 46,000 members. Members of this family are enzymes that metabolize many different compounds, such as steroid hormones, prostaglandins, retinoids, lipids and xenobiotics. Alternative promoter use and alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":23630115,"end":23645639,"strand":1,"description":"dehydrogenase/reductase 2 [Source:HGNC Symbol;Acc:HGNC:18349]"}, {"versioned_ensembl_gene_id":"ENSG00000231194.1","gene_symbol":"FARP1-AS1","gene_name":"FARP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40229]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874080","summary":null,"start":98435405,"end":98435840,"strand":-1,"description":"FARP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40229]"}, {"versioned_ensembl_gene_id":"ENSG00000273394.1","gene_symbol":"AC128687.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113947005,"end":113947570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240776.1","gene_symbol":"AC079944.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113850237,"end":113850731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138018.17","gene_symbol":"SELENOI","gene_name":"selenoprotein I [Source:HGNC Symbol;Acc:HGNC:29361]","synonyms":"SEPI,SELI,KIAA1724,EPT1","biotype":"protein_coding","ncbi_id":"85465","summary":"The multi-pass transmembrane protein encoded by this gene belongs to the CDP-alcohol phosphatidyltransferase class-I family. It catalyzes the transfer of phosphoethanolamine from CDP-ethanolamine to diacylglycerol to produce phosphatidylethanolamine, which is involved in the formation and maintenance of vesicular membranes, regulation of lipid metabolism, and protein folding. This protein is a selenoprotein, containing the rare selenocysteine (Sec) amino acid at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2016]","start":26308547,"end":26395891,"strand":1,"description":"selenoprotein I [Source:HGNC Symbol;Acc:HGNC:29361]"}, {"versioned_ensembl_gene_id":"ENSG00000242444.3","gene_symbol":"AC007207.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":4109661,"end":4118132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257302.1","gene_symbol":"FAHD2P1","gene_name":"fumarylacetoacetate hydrolase domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32441]","synonyms":"FAHD2P","biotype":"processed_pseudogene","ncbi_id":"729610","summary":null,"start":70671918,"end":70672856,"strand":1,"description":"fumarylacetoacetate hydrolase domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32441]"}, {"versioned_ensembl_gene_id":"ENSG00000125861.14","gene_symbol":"GFRA4","gene_name":"GDNF family receptor alpha 4 [Source:HGNC Symbol;Acc:HGNC:13821]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64096","summary":"The protein encoded by this gene is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor for persephin, and mediates activation of the RET tyrosine kinase receptor. This gene is a candidate gene for RET-associated diseases. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":3659292,"end":3663399,"strand":-1,"description":"GDNF family receptor alpha 4 [Source:HGNC Symbol;Acc:HGNC:13821]"}, {"versioned_ensembl_gene_id":"ENSG00000255920.1","gene_symbol":"CCND2-AS2","gene_name":"CCND2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:49399]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106144606","summary":null,"start":4252735,"end":4275065,"strand":-1,"description":"CCND2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:49399]"}, {"versioned_ensembl_gene_id":"ENSG00000118971.7","gene_symbol":"CCND2","gene_name":"cyclin D2 [Source:HGNC Symbol;Acc:HGNC:1583]","synonyms":null,"biotype":"protein_coding","ncbi_id":"894","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK4 or CDK6 and functions as a regulatory subunit of the complex, whose activity is required for cell cycle G1/S transition. This protein has been shown to interact with and be involved in the phosphorylation of tumor suppressor protein Rb. Knockout studies of the homologous gene in mouse suggest the essential roles of this gene in ovarian granulosa and germ cell proliferation. High level expression of this gene was observed in ovarian and testicular tumors. Mutations in this gene are associated with megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 (MPPH3). [provided by RefSeq, Sep 2014]","start":4273772,"end":4305350,"strand":1,"description":"cyclin D2 [Source:HGNC Symbol;Acc:HGNC:1583]"}, {"versioned_ensembl_gene_id":"ENSG00000197085.11","gene_symbol":"NPSR1-AS1","gene_name":"NPSR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:22128]","synonyms":"IMAGE:4827585,AAA1","biotype":"processed_transcript","ncbi_id":"404744","summary":"This gene is located within a region that has been associated with asthma susceptibility. The locus is considered non-protein-coding based on lack of protein homology and a lack of experimental support for an encoded protein. Three alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, May 2010]","start":34346512,"end":34871582,"strand":-1,"description":"NPSR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:22128]"}, {"versioned_ensembl_gene_id":"ENSG00000105963.13","gene_symbol":"ADAP1","gene_name":"ArfGAP with dual PH domains 1 [Source:HGNC Symbol;Acc:HGNC:16486]","synonyms":"GCS1L,CENTA1","biotype":"protein_coding","ncbi_id":"11033","summary":null,"start":897901,"end":955407,"strand":-1,"description":"ArfGAP with dual PH domains 1 [Source:HGNC Symbol;Acc:HGNC:16486]"}, {"versioned_ensembl_gene_id":"ENSG00000232520.1","gene_symbol":"AC012507.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230886500,"end":230897091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237259.1","gene_symbol":"AL049646.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18313765,"end":18315111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125846.15","gene_symbol":"ZNF133","gene_name":"zinc finger protein 133 [Source:HGNC Symbol;Acc:HGNC:12917]","synonyms":"ZNF150,pHZ-66,pHZ-13","biotype":"protein_coding","ncbi_id":"7692","summary":null,"start":18288283,"end":18316996,"strand":1,"description":"zinc finger protein 133 [Source:HGNC Symbol;Acc:HGNC:12917]"}, {"versioned_ensembl_gene_id":"ENSG00000140474.12","gene_symbol":"ULK3","gene_name":"unc-51 like kinase 3 [Source:HGNC Symbol;Acc:HGNC:19703]","synonyms":"FLJ90566,DKFZP434C131","biotype":"protein_coding","ncbi_id":"25989","summary":null,"start":74836116,"end":74843346,"strand":-1,"description":"unc-51 like kinase 3 [Source:HGNC Symbol;Acc:HGNC:19703]"}, {"versioned_ensembl_gene_id":"ENSG00000241280.1","gene_symbol":"AC106712.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101960358,"end":101997926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224328.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"antisense_RNA","ncbi_id":"106478956","summary":null,"start":30703067,"end":30713184,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000225382.1","gene_symbol":"CR759912.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30580177,"end":30583131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244361.1","gene_symbol":"RPL30P7","gene_name":"ribosomal protein L30 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36402]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270979","summary":null,"start":10488820,"end":10489142,"strand":1,"description":"ribosomal protein L30 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36402]"}, {"versioned_ensembl_gene_id":"ENSG00000243771.1","gene_symbol":"AC010618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17589595,"end":17590071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272114.1","gene_symbol":"AL136131.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43770429,"end":43770616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225264.3","gene_symbol":"ZNRF2P2","gene_name":"zinc and ring finger 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42793]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100271874","summary":null,"start":29598795,"end":29685255,"strand":-1,"description":"zinc and ring finger 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42793]"}, {"versioned_ensembl_gene_id":"ENSG00000242222.1","gene_symbol":"AC092989.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135925891,"end":135926167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274332.3","gene_symbol":"LRRC37A2","gene_name":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]","synonyms":"FLJ45049,FLJ45049","biotype":"protein_coding","ncbi_id":"474170","summary":null,"start":45505209,"end":45550562,"strand":-1,"description":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]"}, {"versioned_ensembl_gene_id":"ENSG00000261260.1","gene_symbol":"AC106736.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71301583,"end":71302869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270482.1","gene_symbol":"AC026367.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118375350,"end":118376275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249166.1","gene_symbol":"AC092336.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10493291,"end":10494094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176714.9","gene_symbol":"CCDC121","gene_name":"coiled-coil domain containing 121 [Source:HGNC Symbol;Acc:HGNC:25833]","synonyms":"FLJ43364,FLJ13646","biotype":"protein_coding","ncbi_id":"79635","summary":null,"start":27625639,"end":27629012,"strand":-1,"description":"coiled-coil domain containing 121 [Source:HGNC Symbol;Acc:HGNC:25833]"}, {"versioned_ensembl_gene_id":"ENSG00000223437.1","gene_symbol":"TMSB4XP3","gene_name":"thymosin beta 4, X-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38587]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873877","summary":null,"start":29625870,"end":29625983,"strand":1,"description":"thymosin beta 4, X-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38587]"}, {"versioned_ensembl_gene_id":"ENSG00000249396.1","gene_symbol":"LINC02212","gene_name":"long intergenic non-protein coding RNA 2212 [Source:HGNC Symbol;Acc:HGNC:53079]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929412","summary":null,"start":10493527,"end":10502728,"strand":-1,"description":"long intergenic non-protein coding RNA 2212 [Source:HGNC Symbol;Acc:HGNC:53079]"}, {"versioned_ensembl_gene_id":"ENSG00000111707.11","gene_symbol":"SUDS3","gene_name":"SDS3 homolog, SIN3A corepressor complex component [Source:HGNC Symbol;Acc:HGNC:29545]","synonyms":"SDS3,SAP45,FLJ00052","biotype":"protein_coding","ncbi_id":"64426","summary":"SDS3 is a subunit of the histone deacetylase (see HDAC1; MIM 601241)-dependent SIN3A (MIM 607776) corepressor complex (Fleischer et al., 2003 [PubMed 12724404]).[supplied by OMIM, Mar 2008]","start":118376380,"end":118418031,"strand":1,"description":"SDS3 homolog, SIN3A corepressor complex component [Source:HGNC Symbol;Acc:HGNC:29545]"}, {"versioned_ensembl_gene_id":"ENSG00000188501.11","gene_symbol":"LCTL","gene_name":"lactase like [Source:HGNC Symbol;Acc:HGNC:15583]","synonyms":"KLPH,KLG,FLJ33279","biotype":"protein_coding","ncbi_id":"197021","summary":"This gene encodes a member of family 1 glycosidases. Glycosidases are enzymes that hydrolyze glycosidic bonds and are classified into families based on primary amino acid sequence. Most members of family 1 have two conserved glutamic acid residues, which are required for enzymatic activity. The mouse ortholog of this protein has been characterized and has a domain structure of an N-terminal signal peptide, glycosidase domain, transmembrane domain, and a short cytoplasmic tail. It lacks one of the conserved glutamic acid residues important for catalysis, and its function remains to be determined (PMID: 12084582). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":66547179,"end":66565979,"strand":-1,"description":"lactase like [Source:HGNC Symbol;Acc:HGNC:15583]"}, {"versioned_ensembl_gene_id":"ENSG00000214562.14","gene_symbol":"NUTM2D","gene_name":"NUT family member 2D [Source:HGNC Symbol;Acc:HGNC:23447]","synonyms":"FAM22D","biotype":"protein_coding","ncbi_id":"728130","summary":null,"start":87357668,"end":87370695,"strand":1,"description":"NUT family member 2D [Source:HGNC Symbol;Acc:HGNC:23447]"}, {"versioned_ensembl_gene_id":"ENSG00000147613.7","gene_symbol":"PSKH2","gene_name":"protein serine kinase H2 [Source:HGNC Symbol;Acc:HGNC:18997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85481","summary":null,"start":86048373,"end":86088621,"strand":-1,"description":"protein serine kinase H2 [Source:HGNC Symbol;Acc:HGNC:18997]"}, {"versioned_ensembl_gene_id":"ENSG00000198522.13","gene_symbol":"GPN1","gene_name":"GPN-loop GTPase 1 [Source:HGNC Symbol;Acc:HGNC:17030]","synonyms":"XAB1,RPAP4,NTPBP,MBDIN,ATPBD1A","biotype":"protein_coding","ncbi_id":"11321","summary":"This gene encodes a guanosine triphosphatase enzyme. The encoded protein may play a role in DNA repair and may function in activation of transcription. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":27628247,"end":27651508,"strand":1,"description":"GPN-loop GTPase 1 [Source:HGNC Symbol;Acc:HGNC:17030]"}, {"versioned_ensembl_gene_id":"ENSG00000249160.4","gene_symbol":"LINC02213","gene_name":"long intergenic non-protein coding RNA 2213 [Source:HGNC Symbol;Acc:HGNC:53080]","synonyms":null,"biotype":"lincRNA","ncbi_id":"389273","summary":null,"start":10504996,"end":10522084,"strand":-1,"description":"long intergenic non-protein coding RNA 2213 [Source:HGNC Symbol;Acc:HGNC:53080]"}, {"versioned_ensembl_gene_id":"ENSG00000170044.8","gene_symbol":"ZPLD1","gene_name":"zona pellucida like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27022]","synonyms":null,"biotype":"protein_coding","ncbi_id":"131368","summary":null,"start":102099244,"end":102479841,"strand":1,"description":"zona pellucida like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27022]"}, {"versioned_ensembl_gene_id":"ENSG00000231162.4","gene_symbol":"COX11P1","gene_name":"COX11, cytochrome c oxidase copper chaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2262]","synonyms":"COX11P","biotype":"processed_pseudogene","ncbi_id":"140468","summary":null,"start":28446973,"end":28447807,"strand":1,"description":"COX11, cytochrome c oxidase copper chaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2262]"}, {"versioned_ensembl_gene_id":"ENSG00000272672.1","gene_symbol":"AL391497.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89939601,"end":89940147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261131.1","gene_symbol":"AC012186.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46660696,"end":46661591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256021.1","gene_symbol":"ELOCP31","gene_name":"elongin C pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49172]","synonyms":"TCEB1P31","biotype":"processed_pseudogene","ncbi_id":"100422582","summary":null,"start":21447545,"end":21448314,"strand":-1,"description":"elongin C pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49172]"}, {"versioned_ensembl_gene_id":"ENSG00000228175.3","gene_symbol":"GEMIN8P4","gene_name":"gem nuclear organelle associated protein 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37979]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"492303","summary":null,"start":89993593,"end":89994321,"strand":-1,"description":"gem nuclear organelle associated protein 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37979]"}, {"versioned_ensembl_gene_id":"ENSG00000253675.1","gene_symbol":"AC023194.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86098965,"end":86154225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069329.16","gene_symbol":"VPS35","gene_name":"VPS35, retromer complex component [Source:HGNC Symbol;Acc:HGNC:13487]","synonyms":"PARK17,MEM3,FLJ10752","biotype":"protein_coding","ncbi_id":"55737","summary":"This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the retromer complex, involved in retrograde transport of proteins from endosomes to the trans-Golgi network. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with VPS35, which serves as the core of the retromer complex. [provided by RefSeq, Jul 2008]","start":46656132,"end":46689518,"strand":-1,"description":"VPS35, retromer complex component [Source:HGNC Symbol;Acc:HGNC:13487]"}, {"versioned_ensembl_gene_id":"ENSG00000280017.1","gene_symbol":"AC112200.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10541454,"end":10543192,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004700.15","gene_symbol":"RECQL","gene_name":"RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:9948]","synonyms":"RecQL1,RecQ1","biotype":"protein_coding","ncbi_id":"5965","summary":"The protein encoded by this gene is a member of the RecQ DNA helicase family. DNA helicases are enzymes involved in various types of DNA repair, including mismatch repair, nucleotide excision repair and direct repair. The encoded protein is involved in the processing of Holliday junctions, the suppression of sister chromatid exchanges, telomere maintenance, and is required for genotoxic stress resistance. Defects in this gene have been associated with several types of cancer. [provided by RefSeq, Jan 2017]","start":21468911,"end":21501669,"strand":-1,"description":"RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:9948]"}, {"versioned_ensembl_gene_id":"ENSG00000219262.1","gene_symbol":"Z98745.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28455648,"end":28456141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237671.3","gene_symbol":"GAGE12C","gene_name":"G antigen 12C [Source:HGNC Symbol;Acc:HGNC:28402]","synonyms":"OTTHUMG00000024144","biotype":"protein_coding","ncbi_id":"729422","summary":null,"start":49532211,"end":49539538,"strand":1,"description":"G antigen 12C [Source:HGNC Symbol;Acc:HGNC:28402]"}, {"versioned_ensembl_gene_id":"ENSG00000224384.1","gene_symbol":"AL033379.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96785137,"end":96795821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224914.3","gene_symbol":"LINC00863","gene_name":"long intergenic non-protein coding RNA 863 [Source:HGNC Symbol;Acc:HGNC:45162]","synonyms":null,"biotype":"lincRNA","ncbi_id":"439994","summary":null,"start":87342736,"end":87357882,"strand":1,"description":"long intergenic non-protein coding RNA 863 [Source:HGNC Symbol;Acc:HGNC:45162]"}, {"versioned_ensembl_gene_id":"ENSG00000227753.3","gene_symbol":"AC023194.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86016819,"end":86017126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198862.13","gene_symbol":"LTN1","gene_name":"listerin E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:13082]","synonyms":"ZNF294,RNF160,LISTERIN,KIAA0714,FLJ11053,C21orf98,C21orf10","biotype":"protein_coding","ncbi_id":"26046","summary":"Like most RING finger proteins, LTN1 functions as an E3 ubiquitin ligase (Chu et al., 2009 [PubMed 19196968]).[supplied by OMIM, Nov 2010]","start":28928144,"end":28992956,"strand":-1,"description":"listerin E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:13082]"}, {"versioned_ensembl_gene_id":"ENSG00000197558.11","gene_symbol":"SSPO","gene_name":"SCO-spondin [Source:HGNC Symbol;Acc:HGNC:21998]","synonyms":"SCO-spondin,KIAA0543,FLJ36112","biotype":"protein_coding","ncbi_id":"23145","summary":null,"start":149776042,"end":149833979,"strand":1,"description":"SCO-spondin [Source:HGNC Symbol;Acc:HGNC:21998]"}, {"versioned_ensembl_gene_id":"ENSG00000147614.3","gene_symbol":"ATP6V0D2","gene_name":"ATPase H+ transporting V0 subunit d2 [Source:HGNC Symbol;Acc:HGNC:18266]","synonyms":"VMA6,FLJ38708,ATP6D2","biotype":"protein_coding","ncbi_id":"245972","summary":null,"start":85987323,"end":86154228,"strand":1,"description":"ATPase H+ transporting V0 subunit d2 [Source:HGNC Symbol;Acc:HGNC:18266]"}, {"versioned_ensembl_gene_id":"ENSG00000259134.5","gene_symbol":"LINC00924","gene_name":"long intergenic non-protein coding RNA 924 [Source:HGNC Symbol;Acc:HGNC:27081]","synonyms":null,"biotype":"lincRNA","ncbi_id":"145820","summary":null,"start":95433095,"end":95507847,"strand":1,"description":"long intergenic non-protein coding RNA 924 [Source:HGNC Symbol;Acc:HGNC:27081]"}, {"versioned_ensembl_gene_id":"ENSG00000183562.3","gene_symbol":"AC131971.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2989863,"end":2991344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234869.1","gene_symbol":"AL021392.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46541495,"end":46548196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258489.3","gene_symbol":"AC027013.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95463592,"end":95493770,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205531.12","gene_symbol":"NAP1L4","gene_name":"nucleosome assembly protein 1 like 4 [Source:HGNC Symbol;Acc:HGNC:7640]","synonyms":"NAP2","biotype":"protein_coding","ncbi_id":"4676","summary":"This gene encodes a member of the nucleosome assembly protein (NAP) family which can interact with both core and linker histones. It can shuttle between the cytoplasm and nucleus, suggesting a role as a histone chaperone. This gene is one of several located near the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. [provided by RefSeq, Jul 2008]","start":2944431,"end":2992377,"strand":-1,"description":"nucleosome assembly protein 1 like 4 [Source:HGNC Symbol;Acc:HGNC:7640]"}, {"versioned_ensembl_gene_id":"ENSG00000149021.6","gene_symbol":"SCGB1A1","gene_name":"secretoglobin family 1A member 1 [Source:HGNC Symbol;Acc:HGNC:12523]","synonyms":"UGB,CCSP,CC16,CC10","biotype":"protein_coding","ncbi_id":"7356","summary":"This gene encodes a member of the secretoglobin family of small secreted proteins. The encoded protein has been implicated in numerous functions including anti-inflammation, inhibition of phospholipase A2 and the sequestering of hydrophobic ligands. Defects in this gene are associated with a susceptibility to asthma. [provided by RefSeq, May 2010]","start":62405103,"end":62423195,"strand":1,"description":"secretoglobin family 1A member 1 [Source:HGNC Symbol;Acc:HGNC:12523]"}, {"versioned_ensembl_gene_id":"ENSG00000251691.2","gene_symbol":"AC114786.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69306469,"end":69307173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254288.1","gene_symbol":"AC087672.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74052340,"end":74099853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240047.2","gene_symbol":"AC087672.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74055882,"end":74056647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274406.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832654,"end":54848284,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000254793.1","gene_symbol":"FDPSP4","gene_name":"farnesyl diphosphate synthase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3635]","synonyms":"FPSL4,FDPSL4,CHR39B","biotype":"processed_pseudogene","ncbi_id":"2228","summary":null,"start":42939310,"end":42940358,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3635]"}, {"versioned_ensembl_gene_id":"ENSG00000274942.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754928,"end":54766523,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000255446.1","gene_symbol":"AP003064.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62421845,"end":62426724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243761.1","gene_symbol":"AC023194.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86043102,"end":86043507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122870.11","gene_symbol":"BICC1","gene_name":"BicC family RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19351]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80114","summary":"This gene encodes an RNA-binding protein that is active in regulating gene expression by modulating protein translation during embryonic development. Mouse studies identified the corresponding protein to be under strict control during cell differentiation and to be a maternally provided gene product. [provided by RefSeq, Apr 2009]","start":58513140,"end":58831437,"strand":1,"description":"BicC family RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19351]"}, {"versioned_ensembl_gene_id":"ENSG00000227488.2","gene_symbol":"GAGE12D","gene_name":"G antigen 12D [Source:HGNC Symbol;Acc:HGNC:31904]","synonyms":"OTTHUMG00000024145","biotype":"protein_coding","ncbi_id":"100132399","summary":null,"start":49541767,"end":49549094,"strand":1,"description":"G antigen 12D [Source:HGNC Symbol;Acc:HGNC:31904]"}, {"versioned_ensembl_gene_id":"ENSG00000250612.2","gene_symbol":"AC114786.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69346609,"end":69358177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160691.18","gene_symbol":"SHC1","gene_name":"SHC adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:10840]","synonyms":"ShcA,SHC,p66","biotype":"protein_coding","ncbi_id":"6464","summary":"This gene encodes three main isoforms that differ in activities and subcellular location. While all three are adapter proteins in signal transduction pathways, the longest (p66Shc) may be involved in regulating life span and the effects of reactive oxygen species. The other two isoforms, p52Shc and p46Shc, link activated receptor tyrosine kinases to the Ras pathway by recruitment of the GRB2/SOS complex. p66Shc is not involved in Ras activation. Unlike the other two isoforms, p46Shc is targeted to the mitochondrial matrix. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":154962298,"end":154974395,"strand":-1,"description":"SHC adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:10840]"}, {"versioned_ensembl_gene_id":"ENSG00000236162.1","gene_symbol":"AC092687.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10717773,"end":10720952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248478.2","gene_symbol":"AC104233.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121679126,"end":121707631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284393.1","gene_symbol":"AC092111.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8138140,"end":8175320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255775.1","gene_symbol":"AC005845.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6155035,"end":6160719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249392.1","gene_symbol":"AC096588.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59551142,"end":59630324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273518.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816451,"end":54830756,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000276950.5","gene_symbol":"GSTTP1","gene_name":"glutathione S-transferase theta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26930]","synonyms":"HS322B1A","biotype":"protein_coding","ncbi_id":"25774","summary":null,"start":23998401,"end":24005453,"strand":-1,"description":"glutathione S-transferase theta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26930]"}, {"versioned_ensembl_gene_id":"ENSG00000178031.16","gene_symbol":"ADAMTSL1","gene_name":"ADAMTS like 1 [Source:HGNC Symbol;Acc:HGNC:14632]","synonyms":"FLJ35283,C9orf94,ADAMTSR1","biotype":"protein_coding","ncbi_id":"92949","summary":"This gene encodes a secreted protein and member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) family. This protein lacks the metalloproteinase and disintegrin-like domains, which are typical of the ADAMTS family, but contains other ADAMTS domains, including the thrombospondin type 1 motif. This protein may have important functions in the extracellular matrix. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]","start":17906563,"end":18910950,"strand":1,"description":"ADAMTS like 1 [Source:HGNC Symbol;Acc:HGNC:14632]"}, {"versioned_ensembl_gene_id":"ENSG00000281995.1","gene_symbol":"AC215996.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79610642,"end":79612198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277971.1","gene_symbol":"AC007731.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":20429241,"end":20446620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124257.6","gene_symbol":"NEURL2","gene_name":"neuralized E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16156]","synonyms":"Ozz-E3,Ozz,FLJ30259,dJ337O18.6,C20orf163","biotype":"protein_coding","ncbi_id":"140825","summary":"This gene encodes a protein that is involved in the regulation of myofibril organization. This protein is likely the adaptor component of the E3 ubiquitin ligase complex in striated muscle, and it regulates the ubiquitin-mediated degradation of beta-catenin during myogenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":45888625,"end":45891287,"strand":-1,"description":"neuralized E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:16156]"}, {"versioned_ensembl_gene_id":"ENSG00000268191.1","gene_symbol":"AC010503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6494320,"end":6495025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263667.1","gene_symbol":"AL035696.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181466,"end":205484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269947.1","gene_symbol":"AC135178.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8277763,"end":8278436,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276971.2","gene_symbol":"TRPV6","gene_name":"transient receptor potential cation channel subfamily V member 6 [Source:HGNC Symbol;Acc:HGNC:14006]","synonyms":"ECAC2,CaT1","biotype":"protein_coding","ncbi_id":"55503","summary":"This gene encodes a member of a family of multipass membrane proteins that functions as calcium channels. The encoded protein contains N-terminal ankyrin repeats, which are required for channel assembly and regulation. Translation initiation for this protein occurs at a non-AUG start codon that is decoded as methionine. This gene is situated next to a closely related gene for transient receptor potential cation channel subfamily V member 5 (TRPV5). This locus has experienced positive selection in non-African populations, resulting in several non-synonymous codon differences among individuals of different genetic backgrounds. [provided by RefSeq, Feb 2015]","start":142932365,"end":142946922,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 6 [Source:HGNC Symbol;Acc:HGNC:14006]"}, {"versioned_ensembl_gene_id":"ENSG00000136279.20","gene_symbol":"DBNL","gene_name":"drebrin like [Source:HGNC Symbol;Acc:HGNC:2696]","synonyms":"SH3P7,HIP-55,ABP1","biotype":"protein_coding","ncbi_id":"28988","summary":null,"start":44044640,"end":44069456,"strand":1,"description":"drebrin like [Source:HGNC Symbol;Acc:HGNC:2696]"}, {"versioned_ensembl_gene_id":"ENSG00000273771.1","gene_symbol":"AC024337.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96080713,"end":96084584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276559.2","gene_symbol":"BAAT","gene_name":"bile acid-CoA:amino acid N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:932]","synonyms":"BAT","biotype":"protein_coding","ncbi_id":"570","summary":"The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":101371093,"end":101381063,"strand":-1,"description":"bile acid-CoA:amino acid N-acyltransferase [Source:HGNC Symbol;Acc:HGNC:932]"}, {"versioned_ensembl_gene_id":"ENSG00000135903.18","gene_symbol":"PAX3","gene_name":"paired box 3 [Source:HGNC Symbol;Acc:HGNC:8617]","synonyms":"WS1,HUP2","biotype":"protein_coding","ncbi_id":"5077","summary":"This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]","start":222199888,"end":222298996,"strand":-1,"description":"paired box 3 [Source:HGNC Symbol;Acc:HGNC:8617]"}, {"versioned_ensembl_gene_id":"ENSG00000254346.2","gene_symbol":"MTND1P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42103]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873173","summary":null,"start":33014081,"end":33015026,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42103]"}, {"versioned_ensembl_gene_id":"ENSG00000186970.4","gene_symbol":"KRTAP15-1","gene_name":"keratin associated protein 15-1 [Source:HGNC Symbol;Acc:HGNC:18927]","synonyms":"KAP15.1","biotype":"protein_coding","ncbi_id":"254950","summary":null,"start":30440275,"end":30440945,"strand":1,"description":"keratin associated protein 15-1 [Source:HGNC Symbol;Acc:HGNC:18927]"}, {"versioned_ensembl_gene_id":"ENSG00000198390.4","gene_symbol":"KRTAP13-1","gene_name":"keratin associated protein 13-1 [Source:HGNC Symbol;Acc:HGNC:18924]","synonyms":"KAP13.1","biotype":"protein_coding","ncbi_id":"140258","summary":"Hair keratins and hair keratin-associated proteins (KAPs), such as KRTAP13-1, are the main structural proteins of hair fibers (Rogers et al., 2002 [PubMed 12359730]).[supplied by OMIM, Mar 2008]","start":30396074,"end":30396822,"strand":1,"description":"keratin associated protein 13-1 [Source:HGNC Symbol;Acc:HGNC:18924]"}, {"versioned_ensembl_gene_id":"ENSG00000203645.2","gene_symbol":"LINC00501","gene_name":"long intergenic non-protein coding RNA 501 [Source:HGNC Symbol;Acc:HGNC:43439]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100820709","summary":null,"start":177294442,"end":177323418,"strand":1,"description":"long intergenic non-protein coding RNA 501 [Source:HGNC Symbol;Acc:HGNC:43439]"}, {"versioned_ensembl_gene_id":"ENSG00000257504.1","gene_symbol":"LINC02297","gene_name":"long intergenic non-protein coding RNA 2297 [Source:HGNC Symbol;Acc:HGNC:53214]","synonyms":null,"biotype":"lincRNA","ncbi_id":"642426","summary":null,"start":18630318,"end":18633634,"strand":-1,"description":"long intergenic non-protein coding RNA 2297 [Source:HGNC Symbol;Acc:HGNC:53214]"}, {"versioned_ensembl_gene_id":"ENSG00000213791.4","gene_symbol":"AC104212.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80300869,"end":80301481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168612.4","gene_symbol":"ZSWIM1","gene_name":"zinc finger SWIM-type containing 1 [Source:HGNC Symbol;Acc:HGNC:16155]","synonyms":"dJ337O18.5,C20orf162","biotype":"protein_coding","ncbi_id":"90204","summary":null,"start":45881227,"end":45885266,"strand":1,"description":"zinc finger SWIM-type containing 1 [Source:HGNC Symbol;Acc:HGNC:16155]"}, {"versioned_ensembl_gene_id":"ENSG00000275409.1","gene_symbol":"AC026367.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118430147,"end":118430699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274029.1","gene_symbol":"AC069209.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121190868,"end":121191518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234683.1","gene_symbol":"AL138799.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81596157,"end":81596506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227288.3","gene_symbol":"AL138799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81501794,"end":81503468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215875.4","gene_symbol":"ST13P20","gene_name":"ST13, Hsp70 interacting protein pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38863]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729828","summary":null,"start":81721693,"end":81723068,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:38863]"}, {"versioned_ensembl_gene_id":"ENSG00000241288.7","gene_symbol":"AC092902.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":125827238,"end":125916384,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126768.12","gene_symbol":"TIMM17B","gene_name":"translocase of inner mitochondrial membrane 17B [Source:HGNC Symbol;Acc:HGNC:17310]","synonyms":"JM3,DXS9822","biotype":"protein_coding","ncbi_id":"10245","summary":"This gene encodes a multipass transmembrane protein that forms an integral component of the mitochondrial translocase TIM23 complex. This complex facilitates the transport of mitochondrial proteins from the cytosol across the mitochondrial inner membrane and into the mitochondrion. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":48893447,"end":48898143,"strand":-1,"description":"translocase of inner mitochondrial membrane 17B [Source:HGNC Symbol;Acc:HGNC:17310]"}, {"versioned_ensembl_gene_id":"ENSG00000235374.2","gene_symbol":"SSR4P1","gene_name":"signal sequence receptor subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23131]","synonyms":"PRED90,PRED57,MGC10960,C21orf122","biotype":"transcribed_processed_pseudogene","ncbi_id":"728039","summary":null,"start":45070952,"end":45074165,"strand":-1,"description":"signal sequence receptor subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23131]"}, {"versioned_ensembl_gene_id":"ENSG00000282927.1","gene_symbol":"AC136944.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33484887,"end":33485131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166295.8","gene_symbol":"ANAPC16","gene_name":"anaphase promoting complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:26976]","synonyms":"FLJ33728,CENP-27,C10orf104,bA570G20.3,APC16","biotype":"protein_coding","ncbi_id":"119504","summary":null,"start":72216000,"end":72235860,"strand":1,"description":"anaphase promoting complex subunit 16 [Source:HGNC Symbol;Acc:HGNC:26976]"}, {"versioned_ensembl_gene_id":"ENSG00000120332.15","gene_symbol":"TNN","gene_name":"tenascin N [Source:HGNC Symbol;Acc:HGNC:22942]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63923","summary":null,"start":175067858,"end":175148066,"strand":1,"description":"tenascin N [Source:HGNC Symbol;Acc:HGNC:22942]"}, {"versioned_ensembl_gene_id":"ENSG00000275262.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850443,"end":54867215,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000237389.1","gene_symbol":"AL645634.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43630882,"end":43631564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142327.12","gene_symbol":"RNPEPL1","gene_name":"arginyl aminopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:10079]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57140","summary":null,"start":240565804,"end":240581372,"strand":1,"description":"arginyl aminopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:10079]"}, {"versioned_ensembl_gene_id":"ENSG00000197745.2","gene_symbol":"SCGB1D4","gene_name":"secretoglobin family 1D member 4 [Source:HGNC Symbol;Acc:HGNC:31748]","synonyms":"IIS","biotype":"protein_coding","ncbi_id":"404552","summary":null,"start":62296277,"end":62299064,"strand":-1,"description":"secretoglobin family 1D member 4 [Source:HGNC Symbol;Acc:HGNC:31748]"}, {"versioned_ensembl_gene_id":"ENSG00000186908.14","gene_symbol":"ZDHHC17","gene_name":"zinc finger DHHC-type containing 17 [Source:HGNC Symbol;Acc:HGNC:18412]","synonyms":"KIAA0946,HYPH,HIP14","biotype":"protein_coding","ncbi_id":"23390","summary":null,"start":76763588,"end":76853696,"strand":1,"description":"zinc finger DHHC-type containing 17 [Source:HGNC Symbol;Acc:HGNC:18412]"}, {"versioned_ensembl_gene_id":"ENSG00000054796.12","gene_symbol":"SPO11","gene_name":"SPO11, initiator of meiotic double stranded breaks [Source:HGNC Symbol;Acc:HGNC:11250]","synonyms":"TOPVIA,SPATA43,CT35","biotype":"protein_coding","ncbi_id":"23626","summary":"Meiotic recombination and chromosome segregation require the formation of double-strand breaks (DSBs) in paired chromosome homologs. During meiosis in yeast, a meiotic recombination protein is covalently-linked to the 5' end of DSBs and is essential for the formation of DSBs. The protein encoded by this gene is similar in sequence and conserved features to the yeast meiotic recombination protein. The encoded protein belongs to the TOP6A protein family. Several transcript variants encoding different isoforms have been found for this gene, but the full-length nature of only two of them have been described. [provided by RefSeq, Jul 2008]","start":57329759,"end":57343994,"strand":1,"description":"SPO11, initiator of meiotic double stranded breaks [Source:HGNC Symbol;Acc:HGNC:11250]"}, {"versioned_ensembl_gene_id":"ENSG00000123407.3","gene_symbol":"HOXC12","gene_name":"homeobox C12 [Source:HGNC Symbol;Acc:HGNC:5124]","synonyms":"HOX3F,HOX3,HOC3F","biotype":"protein_coding","ncbi_id":"3228","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. [provided by RefSeq, Jul 2008]","start":53954834,"end":53958956,"strand":1,"description":"homeobox C12 [Source:HGNC Symbol;Acc:HGNC:5124]"}, {"versioned_ensembl_gene_id":"ENSG00000040608.13","gene_symbol":"RTN4R","gene_name":"reticulon 4 receptor [Source:HGNC Symbol;Acc:HGNC:18601]","synonyms":"NOGOR","biotype":"protein_coding","ncbi_id":"65078","summary":"This gene encodes the receptor for reticulon 4, oligodendrocyte myelin glycoprotein and myelin-associated glycoprotein. This receptor mediates axonal growth inhibition and may play a role in regulating axonal regeneration and plasticity in the adult central nervous system. [provided by RefSeq, Jul 2008]","start":20241415,"end":20283246,"strand":-1,"description":"reticulon 4 receptor [Source:HGNC Symbol;Acc:HGNC:18601]"}, {"versioned_ensembl_gene_id":"ENSG00000267752.1","gene_symbol":"AC067796.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23672253,"end":23672748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144362.11","gene_symbol":"PHOSPHO2","gene_name":"phosphatase, orphan 2 [Source:HGNC Symbol;Acc:HGNC:28316]","synonyms":"MGC22679","biotype":"protein_coding","ncbi_id":"493911","summary":null,"start":169694454,"end":169701708,"strand":1,"description":"phosphatase, orphan 2 [Source:HGNC Symbol;Acc:HGNC:28316]"}, {"versioned_ensembl_gene_id":"ENSG00000223853.2","gene_symbol":"CR759766.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573709,"end":29574636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144909.7","gene_symbol":"OSBPL11","gene_name":"oxysterol binding protein like 11 [Source:HGNC Symbol;Acc:HGNC:16397]","synonyms":"ORP-11,FLJ13164,FLJ13012,ORP11","biotype":"protein_coding","ncbi_id":"114885","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Like most members, the encoded protein contains an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. [provided by RefSeq, Jul 2008]","start":125528858,"end":125595090,"strand":-1,"description":"oxysterol binding protein like 11 [Source:HGNC Symbol;Acc:HGNC:16397]"}, {"versioned_ensembl_gene_id":"ENSG00000215274.5","gene_symbol":"GAGE10","gene_name":"G antigen 10 [Source:HGNC Symbol;Acc:HGNC:30968]","synonyms":"OTTHUMG00000024136","biotype":"protein_coding","ncbi_id":"102724473","summary":null,"start":49303669,"end":49319844,"strand":1,"description":"G antigen 10 [Source:HGNC Symbol;Acc:HGNC:30968]"}, {"versioned_ensembl_gene_id":"ENSG00000101440.9","gene_symbol":"ASIP","gene_name":"agouti signaling protein [Source:HGNC Symbol;Acc:HGNC:745]","synonyms":"ASP,AGTIL","biotype":"protein_coding","ncbi_id":"434","summary":"In mice, the agouti gene encodes a paracrine signaling molecule that causes hair follicle melanocytes to synthesize pheomelanin, a yellow pigment, instead of the black or brown pigment, eumelanin. Pleiotropic effects of constitutive expression of the mouse gene include adult-onset obesity, increased tumor susceptibility, and premature infertility. This gene is highly similar to the mouse gene and encodes a secreted protein that may (1) affect the quality of hair pigmentation, (2) act as a pharmacological antagonist of alpha-melanocyte-stimulating hormone, (3) play a role in neuroendocrine aspects of melanocortin action, and (4) have a functional role in regulating lipid metabolism in adipocytes. [provided by RefSeq, Jul 2008]","start":34194569,"end":34269344,"strand":1,"description":"agouti signaling protein [Source:HGNC Symbol;Acc:HGNC:745]"}, {"versioned_ensembl_gene_id":"ENSG00000230961.10","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31779445,"end":31786880,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000162755.13","gene_symbol":"KLHDC9","gene_name":"kelch domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28489]","synonyms":"KARCA1","biotype":"protein_coding","ncbi_id":"126823","summary":null,"start":161098361,"end":161100346,"strand":1,"description":"kelch domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28489]"}, {"versioned_ensembl_gene_id":"ENSG00000246283.2","gene_symbol":"AC090510.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42739118,"end":42743202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260799.1","gene_symbol":"KRT8P50","gene_name":"keratin 8 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48346]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102724430","summary":null,"start":42800968,"end":42802405,"strand":-1,"description":"keratin 8 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48346]"}, {"versioned_ensembl_gene_id":"ENSG00000111249.13","gene_symbol":"CUX2","gene_name":"cut like homeobox 2 [Source:HGNC Symbol;Acc:HGNC:19347]","synonyms":"KIAA0293,CDP2,CUTL2","biotype":"protein_coding","ncbi_id":"23316","summary":"This gene encodes a protein which contains three CUT domains and a homeodomain; both domains are DNA-binding motifs. A similar gene, whose gene product possesses different DNA-binding activities, is located on chromosome on chromosome 7. Two pseudogenes of this gene have been identified on chromosomes 10 and 4. [provided by RefSeq, Jan 2013]","start":111034024,"end":111350554,"strand":1,"description":"cut like homeobox 2 [Source:HGNC Symbol;Acc:HGNC:19347]"}, {"versioned_ensembl_gene_id":"ENSG00000263311.1","gene_symbol":"AC009127.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72004239,"end":72004803,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263688.1","gene_symbol":"AC025887.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32581528,"end":32582828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173862.3","gene_symbol":"AC008080.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33725981,"end":33728456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127989.13","gene_symbol":"MTERF1","gene_name":"mitochondrial transcription termination factor 1 [Source:HGNC Symbol;Acc:HGNC:21463]","synonyms":"MTERF","biotype":"protein_coding","ncbi_id":"7978","summary":"This gene encodes a mitochondrial transcription termination factor. This protein participates in attenuating transcription from the mitochondrial genome; this attenuation allows higher levels of expression of 16S ribosomal RNA relative to the tRNA gene downstream. The product of this gene has three leucine zipper motifs bracketed by two basic domains that are all required for DNA binding. There is evidence that, for this protein, the zippers participate in intramolecular interactions that establish the three-dimensional structure required for DNA binding. [provided by RefSeq, Jul 2008]","start":91692008,"end":91880720,"strand":-1,"description":"mitochondrial transcription termination factor 1 [Source:HGNC Symbol;Acc:HGNC:21463]"}, {"versioned_ensembl_gene_id":"ENSG00000275348.1","gene_symbol":"AC096861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122482990,"end":122483229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188042.7","gene_symbol":"ARL4C","gene_name":"ADP ribosylation factor like GTPase 4C [Source:HGNC Symbol;Acc:HGNC:698]","synonyms":"LAK,ARL7","biotype":"protein_coding","ncbi_id":"10123","summary":"ADP-ribosylation factor-like 4C is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4C is closely similar to ARL4A and ARL4D and each has a nuclear localization signal and an unusually high guanine nucleotide exchange rate. This protein may play a role in cholesterol transport. [provided by RefSeq, Jul 2008]","start":234493041,"end":234497053,"strand":-1,"description":"ADP ribosylation factor like GTPase 4C [Source:HGNC Symbol;Acc:HGNC:698]"}, {"versioned_ensembl_gene_id":"ENSG00000018236.14","gene_symbol":"CNTN1","gene_name":"contactin 1 [Source:HGNC Symbol;Acc:HGNC:2171]","synonyms":"GP135,F3","biotype":"protein_coding","ncbi_id":"1272","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":40692442,"end":41072418,"strand":1,"description":"contactin 1 [Source:HGNC Symbol;Acc:HGNC:2171]"}, {"versioned_ensembl_gene_id":"ENSG00000183463.5","gene_symbol":"URAD","gene_name":"ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase [Source:HGNC Symbol;Acc:HGNC:17785]","synonyms":"PRHOXNB","biotype":"protein_coding","ncbi_id":"646625","summary":null,"start":27977714,"end":27988654,"strand":-1,"description":"ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase [Source:HGNC Symbol;Acc:HGNC:17785]"}, {"versioned_ensembl_gene_id":"ENSG00000132182.11","gene_symbol":"NUP210","gene_name":"nucleoporin 210 [Source:HGNC Symbol;Acc:HGNC:30052]","synonyms":"POM210,KIAA0906,GP210,FLJ22389","biotype":"protein_coding","ncbi_id":"23225","summary":"The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a membrane-spanning glycoprotein that is a major component of the nuclear pore complex. Multiple pseudogenes related to this gene are located on chromosome 3. [provided by RefSeq, Jul 2013]","start":13316235,"end":13420309,"strand":-1,"description":"nucleoporin 210 [Source:HGNC Symbol;Acc:HGNC:30052]"}, {"versioned_ensembl_gene_id":"ENSG00000284452.1","gene_symbol":"AC093326.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":495731,"end":496633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211669.3","gene_symbol":"IGLV3-10","gene_name":"immunoglobulin lambda variable 3-10 [Source:HGNC Symbol;Acc:HGNC:5897]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28803","summary":null,"start":22811747,"end":22812281,"strand":1,"description":"immunoglobulin lambda variable 3-10 [Source:HGNC Symbol;Acc:HGNC:5897]"}, {"versioned_ensembl_gene_id":"ENSG00000274381.1","gene_symbol":"AC245028.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22803076,"end":22803360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250132.6","gene_symbol":"AC004803.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":974133,"end":991190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279408.2","gene_symbol":"AC135068.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21651844,"end":21653039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186212.3","gene_symbol":"SOWAHB","gene_name":"sosondowah ankyrin repeat domain family member B [Source:HGNC Symbol;Acc:HGNC:32958]","synonyms":"ANKRD56","biotype":"protein_coding","ncbi_id":"345079","summary":null,"start":76894928,"end":76898147,"strand":-1,"description":"sosondowah ankyrin repeat domain family member B [Source:HGNC Symbol;Acc:HGNC:32958]"}, {"versioned_ensembl_gene_id":"ENSG00000270971.2","gene_symbol":"REXO1L8P","gene_name":"REXO1 like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:35429]","synonyms":"REXO1L8","biotype":"processed_pseudogene","ncbi_id":"392242","summary":null,"start":85642777,"end":85646325,"strand":-1,"description":"REXO1 like 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:35429]"}, {"versioned_ensembl_gene_id":"ENSG00000160767.20","gene_symbol":"FAM189B","gene_name":"family with sequence similarity 189 member B [Source:HGNC Symbol;Acc:HGNC:1233]","synonyms":"cote1,C1orf2","biotype":"protein_coding","ncbi_id":"10712","summary":"This gene is located near the gene for the lysosomal enzyme glucosylceramidase; a deficiency in this enzyme is associated with Gaucher disease. The encoded protein has been identified as a potential binding partner of a WW domain-containing protein which is involved in apoptosis and tumor suppression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":155247205,"end":155255483,"strand":-1,"description":"family with sequence similarity 189 member B [Source:HGNC Symbol;Acc:HGNC:1233]"}, {"versioned_ensembl_gene_id":"ENSG00000181649.5","gene_symbol":"PHLDA2","gene_name":"pleckstrin homology like domain family A member 2 [Source:HGNC Symbol;Acc:HGNC:12385]","synonyms":"IPL,HLDA2,BWR1C,TSSC3","biotype":"protein_coding","ncbi_id":"7262","summary":"This gene is located in a cluster of imprinted genes on chromosome 11p15.5, which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene has been shown to be imprinted, with preferential expression from the maternal allele in placenta and liver. [provided by RefSeq, Oct 2010]","start":2928273,"end":2929455,"strand":-1,"description":"pleckstrin homology like domain family A member 2 [Source:HGNC Symbol;Acc:HGNC:12385]"}, {"versioned_ensembl_gene_id":"ENSG00000240824.1","gene_symbol":"MTND3P7","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42147]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873183","summary":null,"start":166160777,"end":166161119,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42147]"}, {"versioned_ensembl_gene_id":"ENSG00000278745.1","gene_symbol":"AL391903.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41252696,"end":41252858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215450.2","gene_symbol":"AL022342.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47160838,"end":47161700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254182.1","gene_symbol":"AC106038.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90701082,"end":90701876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169857.7","gene_symbol":"AVEN","gene_name":"apoptosis and caspase activation inhibitor [Source:HGNC Symbol;Acc:HGNC:13509]","synonyms":"PDCD12","biotype":"protein_coding","ncbi_id":"57099","summary":null,"start":33866227,"end":34039176,"strand":-1,"description":"apoptosis and caspase activation inhibitor [Source:HGNC Symbol;Acc:HGNC:13509]"}, {"versioned_ensembl_gene_id":"ENSG00000178971.13","gene_symbol":"CTC1","gene_name":"CST telomere replication complex component 1 [Source:HGNC Symbol;Acc:HGNC:26169]","synonyms":"FLJ22170,C17orf68,AAF132","biotype":"protein_coding","ncbi_id":"80169","summary":"This gene encodes a component of the CST complex. This complex plays an essential role in protecting telomeres from degradation. This protein also forms a heterodimer with the CST complex subunit STN1 to form the enzyme alpha accessory factor. This enzyme regulates DNA replication. Mutations in this gene are the cause of cerebroretinal microangiopathy with calcifications and cysts. Alternate splicing results in both coding and non-coding variants. [provided by RefSeq, Mar 2012]","start":8224821,"end":8248044,"strand":-1,"description":"CST telomere replication complex component 1 [Source:HGNC Symbol;Acc:HGNC:26169]"}, {"versioned_ensembl_gene_id":"ENSG00000236532.5","gene_symbol":"LINC01695","gene_name":"long intergenic non-protein coding RNA 1695 [Source:HGNC Symbol;Acc:HGNC:52483]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927973","summary":null,"start":28116094,"end":28228667,"strand":-1,"description":"long intergenic non-protein coding RNA 1695 [Source:HGNC Symbol;Acc:HGNC:52483]"}, {"versioned_ensembl_gene_id":"ENSG00000164258.11","gene_symbol":"NDUFS4","gene_name":"NADH:ubiquinone oxidoreductase subunit S4 [Source:HGNC Symbol;Acc:HGNC:7711]","synonyms":"CI-18,AQDQ","biotype":"protein_coding","ncbi_id":"4724","summary":"This gene encodes an nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":53560633,"end":53683340,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit S4 [Source:HGNC Symbol;Acc:HGNC:7711]"}, {"versioned_ensembl_gene_id":"ENSG00000228280.1","gene_symbol":"AL731568.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75742740,"end":75743755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170540.14","gene_symbol":"ARL6IP1","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:697]","synonyms":"SPG61,KIAA0069,ARMER,ARL6IP,AIP1","biotype":"protein_coding","ncbi_id":"23204","summary":"This gene belongs to the ARL6ip family and encodes a transmembrane protein that is predominantly localized to intracytoplasmic membranes. It is highly expressed in early myeloid progenitor cells and thought to be involved in protein transport, membrane trafficking, or cell signaling during hematopoietic maturation. Mutations in this gene are associated with spastic paraplegia 61 (SPG61). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]","start":18791667,"end":18801678,"strand":-1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:697]"}, {"versioned_ensembl_gene_id":"ENSG00000204710.2","gene_symbol":"SPDYC","gene_name":"speedy/RINGO cell cycle regulator family member C [Source:HGNC Symbol;Acc:HGNC:32681]","synonyms":"Ringo2","biotype":"protein_coding","ncbi_id":"387778","summary":null,"start":65170154,"end":65173244,"strand":1,"description":"speedy/RINGO cell cycle regulator family member C [Source:HGNC Symbol;Acc:HGNC:32681]"}, {"versioned_ensembl_gene_id":"ENSG00000251191.7","gene_symbol":"LINC00589","gene_name":"long intergenic non-protein coding RNA 589 [Source:HGNC Symbol;Acc:HGNC:32299]","synonyms":"C8orf75","biotype":"lincRNA","ncbi_id":"619351","summary":null,"start":29673922,"end":29748109,"strand":-1,"description":"long intergenic non-protein coding RNA 589 [Source:HGNC Symbol;Acc:HGNC:32299]"}, {"versioned_ensembl_gene_id":"ENSG00000140563.14","gene_symbol":"MCTP2","gene_name":"multiple C2 and transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25636]","synonyms":"FLJ33303,FLJ11175","biotype":"protein_coding","ncbi_id":"55784","summary":null,"start":94231538,"end":94483952,"strand":1,"description":"multiple C2 and transmembrane domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25636]"}, {"versioned_ensembl_gene_id":"ENSG00000112294.12","gene_symbol":"ALDH5A1","gene_name":"aldehyde dehydrogenase 5 family member A1 [Source:HGNC Symbol;Acc:HGNC:408]","synonyms":"SSDH,SSADH","biotype":"protein_coding","ncbi_id":"7915","summary":"This protein belongs to the aldehyde dehydrogenase family of proteins. This gene encodes a mitochondrial NAD(+)-dependent succinic semialdehyde dehydrogenase. A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA). In response to the defect, physiologic fluids from patients accumulate GHB, a compound with numerous neuromodulatory properties. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":24494852,"end":24537207,"strand":1,"description":"aldehyde dehydrogenase 5 family member A1 [Source:HGNC Symbol;Acc:HGNC:408]"}, {"versioned_ensembl_gene_id":"ENSG00000277369.1","gene_symbol":"AC010654.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11797468,"end":11798275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282142.1","gene_symbol":"AC245187.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2517898,"end":2529710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270326.1","gene_symbol":"AL021997.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28319660,"end":28319852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167987.10","gene_symbol":"VPS37C","gene_name":"VPS37C, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:26097]","synonyms":"FLJ20847","biotype":"protein_coding","ncbi_id":"55048","summary":"VPS37C is a subunit of ESCRT-I (endosomal sorting complex required for transport I), a complex in the class E vacuolar protein sorting (VPS) pathway required for sorting ubiquitinated transmembrane proteins into internal vesicles of multivesicular bodies (Eastman et al., 2005 [PubMed 15509564]).[supplied by OMIM, Mar 2008]","start":61130256,"end":61161617,"strand":-1,"description":"VPS37C, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:26097]"}, {"versioned_ensembl_gene_id":"ENSG00000161328.10","gene_symbol":"LRRC56","gene_name":"leucine rich repeat containing 56 [Source:HGNC Symbol;Acc:HGNC:25430]","synonyms":"FLJ00101,DKFZp761L1518","biotype":"protein_coding","ncbi_id":"115399","summary":null,"start":537527,"end":554916,"strand":1,"description":"leucine rich repeat containing 56 [Source:HGNC Symbol;Acc:HGNC:25430]"}, {"versioned_ensembl_gene_id":"ENSG00000228909.1","gene_symbol":"LINC01803","gene_name":"long intergenic non-protein coding RNA 1803 [Source:HGNC Symbol;Acc:HGNC:52595]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373889","summary":null,"start":219904051,"end":219904889,"strand":-1,"description":"long intergenic non-protein coding RNA 1803 [Source:HGNC Symbol;Acc:HGNC:52595]"}, {"versioned_ensembl_gene_id":"ENSG00000135250.16","gene_symbol":"SRPK2","gene_name":"SRSF protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:11306]","synonyms":"SFRSK2","biotype":"protein_coding","ncbi_id":"6733","summary":null,"start":105110704,"end":105399308,"strand":-1,"description":"SRSF protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:11306]"}, {"versioned_ensembl_gene_id":"ENSG00000122376.11","gene_symbol":"FAM35A","gene_name":"family with sequence similarity 35 member A [Source:HGNC Symbol;Acc:HGNC:28773]","synonyms":"MGC5560,FAM35A1,bA163M19.1","biotype":"protein_coding","ncbi_id":"54537","summary":null,"start":87094161,"end":87191468,"strand":1,"description":"family with sequence similarity 35 member A [Source:HGNC Symbol;Acc:HGNC:28773]"}, {"versioned_ensembl_gene_id":"ENSG00000134371.10","gene_symbol":"CDC73","gene_name":"cell division cycle 73 [Source:HGNC Symbol;Acc:HGNC:16783]","synonyms":"parafibromin,HRPT2,HRPT1,FIHP,C1orf28","biotype":"protein_coding","ncbi_id":"79577","summary":"This gene encodes a tumor suppressor that is involved in transcriptional and post-transcriptional control pathways. The protein is a component of the the PAF protein complex, which associates with the RNA polymerase II subunit POLR2A and with a histone methyltransferase complex. This protein appears to facilitate the association of 3' mRNA processing factors with actively-transcribed chromatin. Mutations in this gene have been linked to hyperparathyroidism-jaw tumor syndrome, familial isolated hyperparathyroidism, and parathyroid carcinoma. [provided by RefSeq, Jul 2009]","start":193122017,"end":193253901,"strand":1,"description":"cell division cycle 73 [Source:HGNC Symbol;Acc:HGNC:16783]"}, {"versioned_ensembl_gene_id":"ENSG00000127507.17","gene_symbol":"ADGRE2","gene_name":"adhesion G protein-coupled receptor E2 [Source:HGNC Symbol;Acc:HGNC:3337]","synonyms":"CD312,EMR2","biotype":"protein_coding","ncbi_id":"30817","summary":"This gene encodes a member of the class B seven-span transmembrane (TM7) subfamily of G-protein coupled receptors. These proteins are characterized by an extended extracellular region with a variable number of N-terminal epidermal growth factor-like domains coupled to a TM7 domain via a mucin-like spacer domain. The encoded protein is expressed mainly in myeloid cells where it promotes cell-cell adhesion through interaction with chondroitin sulfate chains. This gene is situated in a cluster of related genes on chromosome 19. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":14732393,"end":14778541,"strand":-1,"description":"adhesion G protein-coupled receptor E2 [Source:HGNC Symbol;Acc:HGNC:3337]"}, {"versioned_ensembl_gene_id":"ENSG00000188234.13","gene_symbol":"AGAP4","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 4 [Source:HGNC Symbol;Acc:HGNC:23459]","synonyms":"MRIP2,Em:AC012044.1,CTGLF5,CTGLF1,AGAP8","biotype":"protein_coding","ncbi_id":"119016","summary":null,"start":45825594,"end":45853875,"strand":-1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 4 [Source:HGNC Symbol;Acc:HGNC:23459]"}, {"versioned_ensembl_gene_id":"ENSG00000224110.3","gene_symbol":"MTRF1LP2","gene_name":"mitochondrial translational release factor 1 like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130376","summary":null,"start":129728744,"end":129730445,"strand":1,"description":"mitochondrial translational release factor 1 like pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50612]"}, {"versioned_ensembl_gene_id":"ENSG00000274429.2","gene_symbol":"DLG5","gene_name":"discs large MAGUK scaffold protein 5 [Source:HGNC Symbol;Acc:HGNC:2904]","synonyms":"P-dlg,KIAA0583","biotype":"protein_coding","ncbi_id":"9231","summary":"This gene encodes a member of the family of discs large (DLG) homologs, a subset of the membrane-associated guanylate kinase (MAGUK) superfamily. The MAGUK proteins are composed of a catalytically inactive guanylate kinase domain, in addition to PDZ and SH3 domains, and are thought to function as scaffolding molecules at sites of cell-cell contact. The protein encoded by this gene localizes to the plasma membrane and cytoplasm, and interacts with components of adherens junctions and the cytoskeleton. It is proposed to function in the transmission of extracellular signals to the cytoskeleton and in the maintenance of epithelial cell structure. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":77790791,"end":77926526,"strand":-1,"description":"discs large MAGUK scaffold protein 5 [Source:HGNC Symbol;Acc:HGNC:2904]"}, {"versioned_ensembl_gene_id":"ENSG00000228549.3","gene_symbol":"BX284668.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16870945,"end":16874092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242078.1","gene_symbol":"AC084864.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129783370,"end":129785185,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134363.11","gene_symbol":"FST","gene_name":"follistatin [Source:HGNC Symbol;Acc:HGNC:3971]","synonyms":"FS","biotype":"protein_coding","ncbi_id":"10468","summary":" Follistatin is a single-chain gonadal protein that specifically inhibits follicle-stimulating hormone release. The single FST gene encodes two isoforms, FST317 and FST344 containing 317 and 344 amino acids respectively, resulting from alternative splicing of the precursor mRNA. In a study in which 37 candidate genes were tested for linkage and association with polycystic ovary syndrome (PCOS) or hyperandrogenemia in 150 families, evidence was found for linkage between PCOS and follistatin. [provided by RefSeq, Jul 2008]","start":53480409,"end":53487134,"strand":1,"description":"follistatin [Source:HGNC Symbol;Acc:HGNC:3971]"}, {"versioned_ensembl_gene_id":"ENSG00000276593.1","gene_symbol":"AC022306.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49353485,"end":49354034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163157.14","gene_symbol":"TMOD4","gene_name":"tropomodulin 4 [Source:HGNC Symbol;Acc:HGNC:11874]","synonyms":"Sk-Tmod","biotype":"protein_coding","ncbi_id":"29765","summary":null,"start":151169986,"end":151176284,"strand":-1,"description":"tropomodulin 4 [Source:HGNC Symbol;Acc:HGNC:11874]"}, {"versioned_ensembl_gene_id":"ENSG00000160973.7","gene_symbol":"FOXH1","gene_name":"forkhead box H1 [Source:HGNC Symbol;Acc:HGNC:3814]","synonyms":"FAST1","biotype":"protein_coding","ncbi_id":"8928","summary":"FOXH1 encodes a human homolog of Xenopus forkhead activin signal transducer-1. FOXH1 protein binds SMAD2 and activates an activin response element via binding the DNA motif TGT(G/T)(T/G)ATT. [provided by RefSeq, Jul 2008]","start":144473412,"end":144476335,"strand":-1,"description":"forkhead box H1 [Source:HGNC Symbol;Acc:HGNC:3814]"}, {"versioned_ensembl_gene_id":"ENSG00000197496.5","gene_symbol":"SLC2A10","gene_name":"solute carrier family 2 member 10 [Source:HGNC Symbol;Acc:HGNC:13444]","synonyms":"GLUT10","biotype":"protein_coding","ncbi_id":"81031","summary":"This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009]","start":46709487,"end":46736347,"strand":1,"description":"solute carrier family 2 member 10 [Source:HGNC Symbol;Acc:HGNC:13444]"}, {"versioned_ensembl_gene_id":"ENSG00000106460.18","gene_symbol":"TMEM106B","gene_name":"transmembrane protein 106B [Source:HGNC Symbol;Acc:HGNC:22407]","synonyms":"MGC33727,FLJ11273","biotype":"protein_coding","ncbi_id":"54664","summary":null,"start":12211241,"end":12243367,"strand":1,"description":"transmembrane protein 106B [Source:HGNC Symbol;Acc:HGNC:22407]"}, {"versioned_ensembl_gene_id":"ENSG00000214607.2","gene_symbol":"ADAM24P","gene_name":"ADAM metallopeptidase domain 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:203]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646479","summary":null,"start":17469518,"end":17471618,"strand":1,"description":"ADAM metallopeptidase domain 24, pseudogene [Source:HGNC Symbol;Acc:HGNC:203]"}, {"versioned_ensembl_gene_id":"ENSG00000196754.10","gene_symbol":"S100A2","gene_name":"S100 calcium binding protein A2 [Source:HGNC Symbol;Acc:HGNC:10492]","synonyms":"S100L,CAN19","biotype":"protein_coding","ncbi_id":"6273","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may have a tumor suppressor function. Chromosomal rearrangements and altered expression of this gene have been implicated in breast cancer. [provided by RefSeq, Jul 2008]","start":153561108,"end":153567890,"strand":-1,"description":"S100 calcium binding protein A2 [Source:HGNC Symbol;Acc:HGNC:10492]"}, {"versioned_ensembl_gene_id":"ENSG00000272556.2","gene_symbol":"GTF2IP13","gene_name":"general transcription factor IIi pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51725]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101929008","summary":null,"start":45769105,"end":45815263,"strand":1,"description":"general transcription factor IIi pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51725]"}, {"versioned_ensembl_gene_id":"ENSG00000065615.13","gene_symbol":"CYB5R4","gene_name":"cytochrome b5 reductase 4 [Source:HGNC Symbol;Acc:HGNC:20147]","synonyms":"NCB5OR,dJ676J13.1,b5+b5R","biotype":"protein_coding","ncbi_id":"51167","summary":"NCB5OR is a flavohemoprotein that contains functional domains found in both cytochrome b5 (CYB5A; MIM 613218) and CYB5 reductase (CYB5R3; MIM 613213) (Zhu et al., 1999 [PubMed 10611283]).[supplied by OMIM, Jan 2010]","start":83859643,"end":83967424,"strand":1,"description":"cytochrome b5 reductase 4 [Source:HGNC Symbol;Acc:HGNC:20147]"}, {"versioned_ensembl_gene_id":"ENSG00000223990.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33013645,"end":33019231,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000233578.1","gene_symbol":"EIF4EP1","gene_name":"eukaryotic translation initiation factor 4E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3292]","synonyms":"EIF4EL2,dJ1022P6.3","biotype":"processed_pseudogene","ncbi_id":"1980","summary":null,"start":5548840,"end":5549481,"strand":1,"description":"eukaryotic translation initiation factor 4E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3292]"}, {"versioned_ensembl_gene_id":"ENSG00000258350.1","gene_symbol":"SYF2P1","gene_name":"SYF2 pre-mRNA splicing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19925]","synonyms":"SYF2P,CBPINP","biotype":"processed_pseudogene","ncbi_id":"317778","summary":null,"start":30541776,"end":30542188,"strand":-1,"description":"SYF2 pre-mRNA splicing factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19925]"}, {"versioned_ensembl_gene_id":"ENSG00000066422.4","gene_symbol":"ZBTB11","gene_name":"zinc finger and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:16740]","synonyms":"ZNF913,ZNF-U69274","biotype":"protein_coding","ncbi_id":"27107","summary":null,"start":101648889,"end":101677495,"strand":-1,"description":"zinc finger and BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:16740]"}, {"versioned_ensembl_gene_id":"ENSG00000256628.3","gene_symbol":"ZBTB11-AS1","gene_name":"ZBTB11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48573]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100009676","summary":null,"start":101676475,"end":101679217,"strand":1,"description":"ZBTB11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48573]"}, {"versioned_ensembl_gene_id":"ENSG00000141434.11","gene_symbol":"MEP1B","gene_name":"meprin A subunit beta [Source:HGNC Symbol;Acc:HGNC:7020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4225","summary":"Meprins are multidomain zinc metalloproteases that are highly expressed in mammalian kidney and intestinal brush border membranes, and in leukocytes and certain cancer cells. They are involved in the hydrolysis of a variety of peptide and protein substrates, and have been implicated in cancer and intestinal inflammation. Mature meprins are oligomers of evolutionarily related, but separately encoded alpha and/or beta subunits. Homooligomers of alpha subunit are secreted, whereas, oligomers containing the beta subunit are plasma membrane-bound. This gene encodes the beta subunit. Targeted disruption of this gene in mice affects embryonic viability, renal gene expression profiles, and distribution of the membrane-associated alpha subunit in kidney and intestine. [provided by RefSeq, Oct 2011]","start":32185069,"end":32220404,"strand":1,"description":"meprin A subunit beta [Source:HGNC Symbol;Acc:HGNC:7020]"}, {"versioned_ensembl_gene_id":"ENSG00000265008.1","gene_symbol":"AC011825.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32091295,"end":32092119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263904.1","gene_symbol":"AC015563.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32245946,"end":32249032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178597.6","gene_symbol":"PSAPL1","gene_name":"prosaposin-like 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:33131]","synonyms":null,"biotype":"protein_coding","ncbi_id":"768239","summary":"This gene encodes a protein that is related to the glycoprotein prosaposin. Based on sequence similarity between the encoded protein and prosaposin, it is predicted that the encoded protein is a preproprotein that is proteolytically processed to generate multiple protein products. These predicted products include saposins A-like, B-like, C-like, and D-like, which may play a role in the lysosomal degradation of sphingolipids. [provided by RefSeq, Jul 2015]","start":7430294,"end":7434973,"strand":-1,"description":"prosaposin-like 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:33131]"}, {"versioned_ensembl_gene_id":"ENSG00000007237.18","gene_symbol":"GAS7","gene_name":"growth arrest specific 7 [Source:HGNC Symbol;Acc:HGNC:4169]","synonyms":"MGC1348,KIAA0394","biotype":"protein_coding","ncbi_id":"8522","summary":"Growth arrest-specific 7 is expressed primarily in terminally differentiated brain cells and predominantly in mature cerebellar Purkinje neurons. GAS7 plays a putative role in neuronal development. Several transcript variants encoding proteins which vary in the N-terminus have been described. [provided by RefSeq, Jul 2008]","start":9910609,"end":10198551,"strand":-1,"description":"growth arrest specific 7 [Source:HGNC Symbol;Acc:HGNC:4169]"}, {"versioned_ensembl_gene_id":"ENSG00000248516.1","gene_symbol":"AC105415.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4321962,"end":4334182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141441.15","gene_symbol":"GAREM1","gene_name":"GRB2 associated regulator of MAPK1 subtype 1 [Source:HGNC Symbol;Acc:HGNC:26136]","synonyms":"FLJ21610,FAM59A,C18orf11,GAREM","biotype":"protein_coding","ncbi_id":"64762","summary":"This gene encodes an adaptor protein which functions in the epidermal growth factor (EGF) receptor-mediated signaling pathway. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":32124877,"end":32470484,"strand":-1,"description":"GRB2 associated regulator of MAPK1 subtype 1 [Source:HGNC Symbol;Acc:HGNC:26136]"}, {"versioned_ensembl_gene_id":"ENSG00000224604.1","gene_symbol":"AC008069.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16853820,"end":16855284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121446.18","gene_symbol":"RGSL1","gene_name":"regulator of G protein signaling like 1 [Source:HGNC Symbol;Acc:HGNC:18636]","synonyms":"RGSL2","biotype":"protein_coding","ncbi_id":"353299","summary":null,"start":182409192,"end":182560599,"strand":1,"description":"regulator of G protein signaling like 1 [Source:HGNC Symbol;Acc:HGNC:18636]"}, {"versioned_ensembl_gene_id":"ENSG00000214614.2","gene_symbol":"AC142086.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32885194,"end":32888874,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233537.1","gene_symbol":"TEDDM2P","gene_name":"transmembrane epididymal protein 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42447]","synonyms":"TEDDM1P1","biotype":"unitary_pseudogene","ncbi_id":"127671","summary":null,"start":182441577,"end":182442362,"strand":1,"description":"transmembrane epididymal protein 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42447]"}, {"versioned_ensembl_gene_id":"ENSG00000000938.12","gene_symbol":"FGR","gene_name":"FGR proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3697]","synonyms":"c-fgr,SRC2,p55c-fgr","biotype":"protein_coding","ncbi_id":"2268","summary":"This gene is a member of the Src family of protein tyrosine kinases (PTKs). The encoded protein contains N-terminal sites for myristylation and palmitylation, a PTK domain, and SH2 and SH3 domains which are involved in mediating protein-protein interactions with phosphotyrosine-containing and proline-rich motifs, respectively. The protein localizes to plasma membrane ruffles, and functions as a negative regulator of cell migration and adhesion triggered by the beta-2 integrin signal transduction pathway. Infection with Epstein-Barr virus results in the overexpression of this gene. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":27612064,"end":27635277,"strand":-1,"description":"FGR proto-oncogene, Src family tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:3697]"}, {"versioned_ensembl_gene_id":"ENSG00000271002.1","gene_symbol":"AC129492.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8199123,"end":8199437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196544.7","gene_symbol":"BORCS6","gene_name":"BLOC-1 related complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25939]","synonyms":"FLJ20014,C17orf59","biotype":"protein_coding","ncbi_id":"54785","summary":null,"start":8188333,"end":8190907,"strand":-1,"description":"BLOC-1 related complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25939]"}, {"versioned_ensembl_gene_id":"ENSG00000259303.5","gene_symbol":"IGHV2OR16-5","gene_name":"immunoglobulin heavy variable 2/OR16-5 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5579]","synonyms":"IGHV2/OR16-5","biotype":"IG_V_gene","ncbi_id":"100129631","summary":null,"start":32847713,"end":32848156,"strand":1,"description":"immunoglobulin heavy variable 2/OR16-5 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5579]"}, {"versioned_ensembl_gene_id":"ENSG00000236104.2","gene_symbol":"ZBTB22","gene_name":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]","synonyms":"BING1,ZBTB22A,fruitless,ZNF297A,fru,ZNF297","biotype":"protein_coding","ncbi_id":"9278","summary":null,"start":33314406,"end":33317942,"strand":-1,"description":"zinc finger and BTB domain containing 22 [Source:HGNC Symbol;Acc:HGNC:13085]"}, {"versioned_ensembl_gene_id":"ENSG00000283324.1","gene_symbol":"AL355860.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":150887136,"end":150913292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161960.14","gene_symbol":"EIF4A1","gene_name":"eukaryotic translation initiation factor 4A1 [Source:HGNC Symbol;Acc:HGNC:3282]","synonyms":"EIF4A,EIF-4A,DDX2A","biotype":"protein_coding","ncbi_id":"1973","summary":null,"start":7572706,"end":7579005,"strand":1,"description":"eukaryotic translation initiation factor 4A1 [Source:HGNC Symbol;Acc:HGNC:3282]"}, {"versioned_ensembl_gene_id":"ENSG00000229357.1","gene_symbol":"CYCSP51","gene_name":"cytochrome c, somatic pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:24383]","synonyms":"HCP1","biotype":"processed_pseudogene","ncbi_id":"343045","summary":null,"start":150903896,"end":150904213,"strand":1,"description":"cytochrome c, somatic pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:24383]"}, {"versioned_ensembl_gene_id":"ENSG00000232665.2","gene_symbol":"PHBP10","gene_name":"prohibitin pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39289]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418815","summary":null,"start":104647216,"end":104647999,"strand":-1,"description":"prohibitin pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39289]"}, {"versioned_ensembl_gene_id":"ENSG00000166845.13","gene_symbol":"C18orf54","gene_name":"chromosome 18 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:13796]","synonyms":"LAS2,MGC33382","biotype":"protein_coding","ncbi_id":"162681","summary":null,"start":54357917,"end":54385218,"strand":1,"description":"chromosome 18 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:13796]"}, {"versioned_ensembl_gene_id":"ENSG00000219453.1","gene_symbol":"AL133270.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23649496,"end":23649774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272509.1","gene_symbol":"AC087752.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94884609,"end":94885070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260611.1","gene_symbol":"AC106785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35785569,"end":35786887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271334.5","gene_symbol":"LINC02104","gene_name":"long intergenic non-protein coding RNA 2104 [Source:HGNC Symbol;Acc:HGNC:52959]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926940","summary":null,"start":39520431,"end":39524708,"strand":1,"description":"long intergenic non-protein coding RNA 2104 [Source:HGNC Symbol;Acc:HGNC:52959]"}, {"versioned_ensembl_gene_id":"ENSG00000272655.2","gene_symbol":"POLR2J4","gene_name":"RNA polymerase II subunit J4, pseudogene [Source:HGNC Symbol;Acc:HGNC:28195]","synonyms":"MGC13098,MGC13098","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"84820","summary":null,"start":44013562,"end":44019170,"strand":-1,"description":"RNA polymerase II subunit J4, pseudogene [Source:HGNC Symbol;Acc:HGNC:28195]"}, {"versioned_ensembl_gene_id":"ENSG00000217041.1","gene_symbol":"AL512430.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110700562,"end":110700900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264450.1","gene_symbol":"AC004231.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40850800,"end":40863282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128578.9","gene_symbol":"STRIP2","gene_name":"striatin interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:22209]","synonyms":"KIAA1170,FAR11B,FAM40B","biotype":"protein_coding","ncbi_id":"57464","summary":null,"start":129434433,"end":129488399,"strand":1,"description":"striatin interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:22209]"}, {"versioned_ensembl_gene_id":"ENSG00000276836.4","gene_symbol":"ARHGAP27","gene_name":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]","synonyms":"SH3P20,SH3D20,FLJ43547,CAMGAP1","biotype":"protein_coding","ncbi_id":"201176","summary":"This gene encodes a member of a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may pay a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2013]","start":45393920,"end":45434353,"strand":-1,"description":"Rho GTPase activating protein 27 [Source:HGNC Symbol;Acc:HGNC:31813]"}, {"versioned_ensembl_gene_id":"ENSG00000187955.11","gene_symbol":"COL14A1","gene_name":"collagen type XIV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2191]","synonyms":"UND","biotype":"protein_coding","ncbi_id":"7373","summary":"This gene encodes the alpha chain of type XIV collagen, a member of the FACIT (fibril-associated collagens with interrupted triple helices) collagen family. Type XIV collagen interacts with the fibril surface and is involved in the regulation of fibrillogenesis. [provided by RefSeq, Jan 2013]","start":120059780,"end":120372036,"strand":1,"description":"collagen type XIV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2191]"}, {"versioned_ensembl_gene_id":"ENSG00000274939.2","gene_symbol":"TBC1D3B","gene_name":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]","synonyms":"TBC1D3I,PRC17,TBC1D3I,PRC17","biotype":"protein_coding","ncbi_id":"414059","summary":"This gene encodes a protein that is similar to TBC1 domain family, member 3. This protein contains a TBC (Tre-2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q. [provided by RefSeq, Apr 2009]","start":36166057,"end":36176992,"strand":-1,"description":"TBC1 domain family member 3B [Source:HGNC Symbol;Acc:HGNC:27011]"}, {"versioned_ensembl_gene_id":"ENSG00000275347.2","gene_symbol":"AC003976.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36163208,"end":36163292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225151.10","gene_symbol":"GOLGA2P7","gene_name":"golgin A2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49516]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388152","summary":null,"start":84199311,"end":84230136,"strand":-1,"description":"golgin A2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49516]"}, {"versioned_ensembl_gene_id":"ENSG00000233421.4","gene_symbol":"LINC01783","gene_name":"long intergenic non-protein coding RNA 1783 [Source:HGNC Symbol;Acc:HGNC:52573]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132147","summary":null,"start":16533886,"end":16536172,"strand":-1,"description":"long intergenic non-protein coding RNA 1783 [Source:HGNC Symbol;Acc:HGNC:52573]"}, {"versioned_ensembl_gene_id":"ENSG00000225831.1","gene_symbol":"RPS18P1","gene_name":"ribosomal protein S18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16550]","synonyms":"dJ1022P6.1","biotype":"processed_pseudogene","ncbi_id":"128676","summary":null,"start":5532878,"end":5533335,"strand":1,"description":"ribosomal protein S18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16550]"}, {"versioned_ensembl_gene_id":"ENSG00000274971.1","gene_symbol":"GU182353.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771253,"end":54784657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183850.13","gene_symbol":"ZNF730","gene_name":"zinc finger protein 730 [Source:HGNC Symbol;Acc:HGNC:32470]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129543","summary":null,"start":23075210,"end":23147219,"strand":1,"description":"zinc finger protein 730 [Source:HGNC Symbol;Acc:HGNC:32470]"}, {"versioned_ensembl_gene_id":"ENSG00000227537.1","gene_symbol":"AL139281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23258211,"end":23258545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224946.1","gene_symbol":"AC007312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33276834,"end":33277091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159167.11","gene_symbol":"STC1","gene_name":"stanniocalcin 1 [Source:HGNC Symbol;Acc:HGNC:11373]","synonyms":"STC","biotype":"protein_coding","ncbi_id":"6781","summary":"This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The gene contains a 5' UTR rich in CAG trinucleotide repeats. The encoded protein contains 11 conserved cysteine residues and is phosphorylated by protein kinase C exclusively on its serine residues. The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/phosphate homeostasis. Overexpression of human stanniocalcin 1 in mice produces high serum phosphate levels, dwarfism, and increased metabolic rate. This gene has altered expression in hepatocellular, ovarian, and breast cancers. [provided by RefSeq, Jul 2008]","start":23841915,"end":23854807,"strand":-1,"description":"stanniocalcin 1 [Source:HGNC Symbol;Acc:HGNC:11373]"}, {"versioned_ensembl_gene_id":"ENSG00000274334.1","gene_symbol":"VASN","gene_name":"vasorin [Source:HGNC Symbol;Acc:HGNC:18517]","synonyms":"SLITL2","biotype":"protein_coding","ncbi_id":"114990","summary":null,"start":4373807,"end":4385487,"strand":1,"description":"vasorin [Source:HGNC Symbol;Acc:HGNC:18517]"}, {"versioned_ensembl_gene_id":"ENSG00000225676.1","gene_symbol":"AC002378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30184644,"end":30207109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225284.1","gene_symbol":"AC018693.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38861720,"end":38863133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159216.18","gene_symbol":"RUNX1","gene_name":"runt related transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10471]","synonyms":"PEBP2A2,CBFA2,AMLCR1,AML1","biotype":"protein_coding","ncbi_id":"861","summary":"Core binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":34787801,"end":36004667,"strand":-1,"description":"runt related transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10471]"}, {"versioned_ensembl_gene_id":"ENSG00000231300.1","gene_symbol":"EZH2P1","gene_name":"enhancer of zeste 2 polycomb repressive complex 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39918]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266693","summary":null,"start":35599732,"end":35600022,"strand":-1,"description":"enhancer of zeste 2 polycomb repressive complex 2 subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39918]"}, {"versioned_ensembl_gene_id":"ENSG00000237008.2","gene_symbol":"LAPTM4BP1","gene_name":"lysosomal protein transmembrane 4 beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51934]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645900","summary":null,"start":153379821,"end":153380799,"strand":-1,"description":"lysosomal protein transmembrane 4 beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51934]"}, {"versioned_ensembl_gene_id":"ENSG00000282302.2","gene_symbol":"SEPT9","gene_name":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]","synonyms":"MSF1,MSF,KIAA0991,AF17q25,SeptD1,PNUTL4","biotype":"protein_coding","ncbi_id":"10801","summary":"This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]","start":77292191,"end":77306525,"strand":1,"description":"septin 9 [Source:HGNC Symbol;Acc:HGNC:7323]"}, {"versioned_ensembl_gene_id":"ENSG00000198918.7","gene_symbol":"RPL39","gene_name":"ribosomal protein L39 [Source:HGNC Symbol;Acc:HGNC:10350]","synonyms":"RPL39P42,L39","biotype":"protein_coding","ncbi_id":"6170","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the S39E family of ribosomal proteins. It is located in the cytoplasm. In rat, the protein is the smallest, and one of the most basic, proteins of the ribosome. This gene is co-transcribed with the U69 small nucleolar RNA gene, which is located in its second intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":119786504,"end":119791643,"strand":-1,"description":"ribosomal protein L39 [Source:HGNC Symbol;Acc:HGNC:10350]"}, {"versioned_ensembl_gene_id":"ENSG00000109047.7","gene_symbol":"RCVRN","gene_name":"recoverin [Source:HGNC Symbol;Acc:HGNC:9937]","synonyms":"RCV1","biotype":"protein_coding","ncbi_id":"5957","summary":"This gene encodes a member of the recoverin family of neuronal calcium sensors. The encoded protein contains three calcium-binding EF-hand domains and may prolong the termination of the phototransduction cascade in the retina by blocking the phosphorylation of photo-activated rhodopsin. Recoverin may be the antigen responsible for cancer-associated retinopathy. [provided by RefSeq, Jul 2008]","start":9896320,"end":9905621,"strand":-1,"description":"recoverin [Source:HGNC Symbol;Acc:HGNC:9937]"}, {"versioned_ensembl_gene_id":"ENSG00000229163.2","gene_symbol":"NAP1L1P2","gene_name":"nucleosome assembly protein 1 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128894","summary":null,"start":2929001,"end":2931120,"strand":-1,"description":"nucleosome assembly protein 1 like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38005]"}, {"versioned_ensembl_gene_id":"ENSG00000189292.15","gene_symbol":"ALKAL2","gene_name":"ALK and LTK ligand 2 [Source:HGNC Symbol;Acc:HGNC:27683]","synonyms":"FAM150B,AUGA","biotype":"protein_coding","ncbi_id":"285016","summary":null,"start":279558,"end":288851,"strand":-1,"description":"ALK and LTK ligand 2 [Source:HGNC Symbol;Acc:HGNC:27683]"}, {"versioned_ensembl_gene_id":"ENSG00000228643.1","gene_symbol":"AC079779.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":286419,"end":301515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281279.1","gene_symbol":"OR5G4P","gene_name":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81192","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56801280,"end":56802039,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15288]"}, {"versioned_ensembl_gene_id":"ENSG00000137185.11","gene_symbol":"ZSCAN9","gene_name":"zinc finger and SCAN domain containing 9 [Source:HGNC Symbol;Acc:HGNC:12984]","synonyms":"ZNF193,PRD51","biotype":"protein_coding","ncbi_id":"7746","summary":null,"start":28224886,"end":28233482,"strand":1,"description":"zinc finger and SCAN domain containing 9 [Source:HGNC Symbol;Acc:HGNC:12984]"}, {"versioned_ensembl_gene_id":"ENSG00000255165.1","gene_symbol":"AC134775.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44071462,"end":44072403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110455.13","gene_symbol":"ACCS","gene_name":"1-aminocyclopropane-1-carboxylate synthase homolog (inactive) [Source:HGNC Symbol;Acc:HGNC:23989]","synonyms":"PHACS,ACS","biotype":"protein_coding","ncbi_id":"84680","summary":null,"start":44065925,"end":44084222,"strand":1,"description":"1-aminocyclopropane-1-carboxylate synthase homolog (inactive) [Source:HGNC Symbol;Acc:HGNC:23989]"}, {"versioned_ensembl_gene_id":"ENSG00000226033.9","gene_symbol":"STK19","gene_name":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]","synonyms":"D6S60,RP1,G11","biotype":"protein_coding","ncbi_id":"8859","summary":"This gene encodes a serine/threonine kinase which localizes predominantly to the nucleus. Its specific function is unknown; it is possible that phosphorylation of this protein is involved in transcriptional regulation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6 and expresses two transcript variants. [provided by RefSeq, Jul 2008]","start":32047618,"end":32057890,"strand":1,"description":"serine/threonine kinase 19 [Source:HGNC Symbol;Acc:HGNC:11398]"}, {"versioned_ensembl_gene_id":"ENSG00000169562.9","gene_symbol":"GJB1","gene_name":"gap junction protein beta 1 [Source:HGNC Symbol;Acc:HGNC:4283]","synonyms":"CMTX1,CMTX,CX32","biotype":"protein_coding","ncbi_id":"2705","summary":"This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2008]","start":71215194,"end":71225516,"strand":1,"description":"gap junction protein beta 1 [Source:HGNC Symbol;Acc:HGNC:4283]"}, {"versioned_ensembl_gene_id":"ENSG00000106025.8","gene_symbol":"TSPAN12","gene_name":"tetraspanin 12 [Source:HGNC Symbol;Acc:HGNC:21641]","synonyms":"TM4SF12,NET-2","biotype":"protein_coding","ncbi_id":"23554","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. [provided by RefSeq, Jul 2008]","start":120787320,"end":120858402,"strand":-1,"description":"tetraspanin 12 [Source:HGNC Symbol;Acc:HGNC:21641]"}, {"versioned_ensembl_gene_id":"ENSG00000229467.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"HS6M1-14,OR2I2,OR2I4P,OR2I1,OR2I3P","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29549819,"end":29550766,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000237698.1","gene_symbol":"GPR53P","gene_name":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]","synonyms":"dJ271M21.8,PsiGPR53","biotype":"processed_pseudogene","ncbi_id":"9292","summary":null,"start":29534286,"end":29535369,"strand":-1,"description":"G protein-coupled receptor 53, pseudogene [Source:HGNC Symbol;Acc:HGNC:4509]"}, {"versioned_ensembl_gene_id":"ENSG00000162654.8","gene_symbol":"GBP4","gene_name":"guanylate binding protein 4 [Source:HGNC Symbol;Acc:HGNC:20480]","synonyms":"Mpa2","biotype":"protein_coding","ncbi_id":"115361","summary":"Guanylate-binding proteins, such as GBP4, are induced by interferon and hydrolyze GTP to both GDP and GMP (Vestal, 2005 [PubMed 16108726]).[supplied by OMIM, Dec 2008]","start":89181148,"end":89198932,"strand":-1,"description":"guanylate binding protein 4 [Source:HGNC Symbol;Acc:HGNC:20480]"}, {"versioned_ensembl_gene_id":"ENSG00000241045.1","gene_symbol":"RPL7P43","gene_name":"ribosomal protein L7 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36441]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271224","summary":null,"start":76721534,"end":76722286,"strand":1,"description":"ribosomal protein L7 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36441]"}, {"versioned_ensembl_gene_id":"ENSG00000227133.1","gene_symbol":"AC011742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26160023,"end":26161136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178234.12","gene_symbol":"GALNT11","gene_name":"polypeptide N-acetylgalactosaminyltransferase 11 [Source:HGNC Symbol;Acc:HGNC:19875]","synonyms":"GalNAc-T11","biotype":"protein_coding","ncbi_id":"63917","summary":null,"start":152025674,"end":152122347,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 11 [Source:HGNC Symbol;Acc:HGNC:19875]"}, {"versioned_ensembl_gene_id":"ENSG00000226029.1","gene_symbol":"LINC01772","gene_name":"long intergenic non-protein coding RNA 1772 [Source:HGNC Symbol;Acc:HGNC:52562]","synonyms":"ENSG00000226029","biotype":"lincRNA","ncbi_id":"107984921","summary":null,"start":16460948,"end":16468481,"strand":1,"description":"long intergenic non-protein coding RNA 1772 [Source:HGNC Symbol;Acc:HGNC:52562]"}, {"versioned_ensembl_gene_id":"ENSG00000235481.2","gene_symbol":"UBE2R2-AS1","gene_name":"UBE2R2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49911]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929665","summary":null,"start":33785950,"end":33818795,"strand":-1,"description":"UBE2R2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49911]"}, {"versioned_ensembl_gene_id":"ENSG00000124091.9","gene_symbol":"GCNT7","gene_name":"glucosaminyl (N-acetyl) transferase family member 7 [Source:HGNC Symbol;Acc:HGNC:16099]","synonyms":"dJ1153D9.2,C20orf105","biotype":"protein_coding","ncbi_id":"140687","summary":null,"start":56491492,"end":56525925,"strand":-1,"description":"glucosaminyl (N-acetyl) transferase family member 7 [Source:HGNC Symbol;Acc:HGNC:16099]"}, {"versioned_ensembl_gene_id":"ENSG00000165655.16","gene_symbol":"ZNF503","gene_name":"zinc finger protein 503 [Source:HGNC Symbol;Acc:HGNC:23589]","synonyms":"Nlz2,MGC2555,FLJ45745","biotype":"protein_coding","ncbi_id":"84858","summary":null,"start":75397830,"end":75401906,"strand":-1,"description":"zinc finger protein 503 [Source:HGNC Symbol;Acc:HGNC:23589]"}, {"versioned_ensembl_gene_id":"ENSG00000261340.1","gene_symbol":"LINC01616","gene_name":"long intergenic non-protein coding RNA 1616 [Source:HGNC Symbol;Acc:HGNC:51900]","synonyms":"n341006","biotype":"lincRNA","ncbi_id":"106456574","summary":null,"start":29980113,"end":29982392,"strand":-1,"description":"long intergenic non-protein coding RNA 1616 [Source:HGNC Symbol;Acc:HGNC:51900]"}, {"versioned_ensembl_gene_id":"ENSG00000233717.1","gene_symbol":"RPS29P29","gene_name":"ribosomal protein S29 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729145","summary":null,"start":151111912,"end":151112728,"strand":-1,"description":"ribosomal protein S29 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:52362]"}, {"versioned_ensembl_gene_id":"ENSG00000276906.2","gene_symbol":"CU467612.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54396006,"end":54401717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232302.3","gene_symbol":"AL662869.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29485842,"end":29486247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100246.12","gene_symbol":"DNAL4","gene_name":"dynein axonemal light chain 4 [Source:HGNC Symbol;Acc:HGNC:2955]","synonyms":"PIG27,dJ327J16","biotype":"protein_coding","ncbi_id":"10126","summary":"This gene encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. [provided by RefSeq, Dec 2014]","start":38778508,"end":38794198,"strand":-1,"description":"dynein axonemal light chain 4 [Source:HGNC Symbol;Acc:HGNC:2955]"}, {"versioned_ensembl_gene_id":"ENSG00000278678.1","gene_symbol":"CYCSP41","gene_name":"cytochrome c, somatic pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:2580]","synonyms":"HCP41,CYC1LP4","biotype":"processed_pseudogene","ncbi_id":"360186","summary":null,"start":10576292,"end":10576587,"strand":1,"description":"cytochrome c, somatic pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:2580]"}, {"versioned_ensembl_gene_id":"ENSG00000231540.1","gene_symbol":"ELOCP9","gene_name":"elongin C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38145]","synonyms":"TCEB1P9","biotype":"processed_pseudogene","ncbi_id":"100462870","summary":null,"start":23808821,"end":23809059,"strand":-1,"description":"elongin C pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:38145]"}, {"versioned_ensembl_gene_id":"ENSG00000276688.1","gene_symbol":"AL121757.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5407564,"end":5407876,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273808.2","gene_symbol":"ABCC6P2","gene_name":"ATP binding cassette subfamily C member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33353]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"730013","summary":null,"start":15389326,"end":15393236,"strand":1,"description":"ATP binding cassette subfamily C member 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33353]"}, {"versioned_ensembl_gene_id":"ENSG00000147439.12","gene_symbol":"BIN3","gene_name":"bridging integrator 3 [Source:HGNC Symbol;Acc:HGNC:1054]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55909","summary":"The product of this gene is a member of the BAR domain protein family. The encoded protein is comprised solely of a BAR domain which is predicted to form coiled-coil structures and proposed to mediate dimerization, sense and induce membrane curvature, and bind small GTPases. BAR domain proteins have been implicated in endocytosis, intracellular transport, and a diverse set of other processes. [provided by RefSeq, Jul 2008]","start":22620418,"end":22669148,"strand":-1,"description":"bridging integrator 3 [Source:HGNC Symbol;Acc:HGNC:1054]"}, {"versioned_ensembl_gene_id":"ENSG00000274395.1","gene_symbol":"AC126177.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107835541,"end":107836555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272508.1","gene_symbol":"AL136982.6","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":86993432,"end":87024732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101751.10","gene_symbol":"POLI","gene_name":"DNA polymerase iota [Source:HGNC Symbol;Acc:HGNC:9182]","synonyms":"RAD3OB,RAD30B","biotype":"protein_coding","ncbi_id":"11201","summary":"The protein encoded by this gene is an error-prone DNA polymerase involved in DNA repair. The encoded protein promotes DNA synthesis across lesions in the template DNA, which other polymerases cannot do. The encoded polymerase inserts deoxynucleotides across lesions and then relies on DNA polymerase zeta to extend the nascent DNA strand to bypass the lesion. [provided by RefSeq, May 2017]","start":54269404,"end":54321266,"strand":1,"description":"DNA polymerase iota [Source:HGNC Symbol;Acc:HGNC:9182]"}, {"versioned_ensembl_gene_id":"ENSG00000260341.1","gene_symbol":"C2orf69P2","gene_name":"chromosome 2 open reading frame 69 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642614","summary":null,"start":35492324,"end":35493446,"strand":1,"description":"chromosome 2 open reading frame 69 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51801]"}, {"versioned_ensembl_gene_id":"ENSG00000248669.1","gene_symbol":"AC116562.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4117925,"end":4118284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237972.1","gene_symbol":"TUBG1P","gene_name":"tubulin gamma 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:12418]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442673","summary":null,"start":43918697,"end":43920054,"strand":1,"description":"tubulin gamma 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:12418]"}, {"versioned_ensembl_gene_id":"ENSG00000284727.1","gene_symbol":"AC116562.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":4048211,"end":4107583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230244.1","gene_symbol":"RAD23BP2","gene_name":"RAD23 homolog B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44510]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130572","summary":null,"start":83663419,"end":83664625,"strand":1,"description":"RAD23 homolog B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44510]"}, {"versioned_ensembl_gene_id":"ENSG00000213060.4","gene_symbol":"AL031864.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171803517,"end":171803939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162408.10","gene_symbol":"NOL9","gene_name":"nucleolar protein 9 [Source:HGNC Symbol;Acc:HGNC:26265]","synonyms":"NET6,Grc3,FLJ23323","biotype":"protein_coding","ncbi_id":"79707","summary":null,"start":6521347,"end":6554535,"strand":-1,"description":"nucleolar protein 9 [Source:HGNC Symbol;Acc:HGNC:26265]"}, {"versioned_ensembl_gene_id":"ENSG00000278106.1","gene_symbol":"AF254983.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10397644,"end":10397778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100226.15","gene_symbol":"GTPBP1","gene_name":"GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4669]","synonyms":"GP-1,HSPC018","biotype":"protein_coding","ncbi_id":"9567","summary":"This gene is upregulated by interferon-gamma and encodes a protein that is a member of the AGP11/GTPBP1 family of GTP-binding proteins. A structurally similar protein has been found in mouse, where disruption of the gene for that protein had no observable phenotype. [provided by RefSeq, Jul 2008]","start":38705723,"end":38738299,"strand":1,"description":"GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4669]"}, {"versioned_ensembl_gene_id":"ENSG00000174946.6","gene_symbol":"GPR171","gene_name":"G protein-coupled receptor 171 [Source:HGNC Symbol;Acc:HGNC:30057]","synonyms":"H963","biotype":"protein_coding","ncbi_id":"29909","summary":null,"start":151197832,"end":151203201,"strand":-1,"description":"G protein-coupled receptor 171 [Source:HGNC Symbol;Acc:HGNC:30057]"}, {"versioned_ensembl_gene_id":"ENSG00000237015.1","gene_symbol":"AL031186.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29260889,"end":29262037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064995.16","gene_symbol":"TAF11","gene_name":"TATA-box binding protein associated factor 11 [Source:HGNC Symbol;Acc:HGNC:11544]","synonyms":"TAFII28,TAF2I","biotype":"protein_coding","ncbi_id":"6882","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes a small subunit of TFIID that is present in all TFIID complexes and interacts with TBP. This subunit also interacts with another small subunit, TAF13, to form a heterodimer with a structure similar to the histone core structure. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]","start":34877778,"end":34888089,"strand":-1,"description":"TATA-box binding protein associated factor 11 [Source:HGNC Symbol;Acc:HGNC:11544]"}, {"versioned_ensembl_gene_id":"ENSG00000227409.1","gene_symbol":"ZMYM4-AS1","gene_name":"ZMYM4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40624]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861513","summary":null,"start":35358822,"end":35366077,"strand":-1,"description":"ZMYM4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40624]"}, {"versioned_ensembl_gene_id":"ENSG00000159763.3","gene_symbol":"PIP","gene_name":"prolactin induced protein [Source:HGNC Symbol;Acc:HGNC:8993]","synonyms":"GPIP4,GCDFP15,GCDFP-15","biotype":"protein_coding","ncbi_id":"5304","summary":null,"start":143132077,"end":143139746,"strand":1,"description":"prolactin induced protein [Source:HGNC Symbol;Acc:HGNC:8993]"}, {"versioned_ensembl_gene_id":"ENSG00000142453.11","gene_symbol":"CARM1","gene_name":"coactivator associated arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23393]","synonyms":"PRMT4","biotype":"protein_coding","ncbi_id":"10498","summary":"This gene belongs to the protein arginine methyltransferase (PRMT) family. The encoded enzyme catalyzes the methylation of guanidino nitrogens of arginyl residues of proteins. The enzyme acts specifically on histones and other chromatin-associated proteins and is involved in regulation of gene expression. The enzyme may act in association with other proteins or within multi-protein complexes and may play a role in cell type-specific functions and cell lineage specification. A related pseudogene is located on chromosome 9. [provided by RefSeq, Aug 2013]","start":10871513,"end":10923070,"strand":1,"description":"coactivator associated arginine methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:23393]"}, {"versioned_ensembl_gene_id":"ENSG00000225781.1","gene_symbol":"OR6V1","gene_name":"olfactory receptor family 6 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15090]","synonyms":"GPR138","biotype":"protein_coding","ncbi_id":"346517","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143052320,"end":143053347,"strand":1,"description":"olfactory receptor family 6 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:15090]"}, {"versioned_ensembl_gene_id":"ENSG00000206466.10","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"GPRC3A,hGB1a","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555423,"end":29632960,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000255965.1","gene_symbol":"AC073916.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124383381,"end":124383510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224293.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"OTTHUMG00000086663,BPG126D10.10","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577260,"end":29577549,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000223775.8","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"C6orf14,MRPS18-2,HSPC183,PTD017","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30609932,"end":30618618,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000233969.1","gene_symbol":"AC004946.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120168345,"end":120186064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179468.5","gene_symbol":"OR9A2","gene_name":"olfactory receptor family 9 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15093]","synonyms":null,"biotype":"protein_coding","ncbi_id":"135924","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143026158,"end":143027195,"strand":-1,"description":"olfactory receptor family 9 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:15093]"}, {"versioned_ensembl_gene_id":"ENSG00000206468.3","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555423,"end":29559736,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000182974.3","gene_symbol":"AC135068.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21637909,"end":21638992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109452.12","gene_symbol":"INPP4B","gene_name":"inositol polyphosphate-4-phosphatase type II B [Source:HGNC Symbol;Acc:HGNC:6075]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8821","summary":"INPP4B encodes the inositol polyphosphate 4-phosphatase type II, one of the enzymes involved in phosphatidylinositol signaling pathways. This enzyme removes the phosphate group at position 4 of the inositol ring from inositol 3,4-bisphosphate. There is limited data to suggest that the human type II enzyme is subject to alternative splicing, as has been established for the type I enzyme. [provided by RefSeq, Jul 2008]","start":142023160,"end":142847432,"strand":-1,"description":"inositol polyphosphate-4-phosphatase type II B [Source:HGNC Symbol;Acc:HGNC:6075]"}, {"versioned_ensembl_gene_id":"ENSG00000272669.1","gene_symbol":"AL021707.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38742625,"end":38743115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249806.1","gene_symbol":"AC139720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142566019,"end":142660950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225450.1","gene_symbol":"AL021707.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38739003,"end":38749041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214978.7","gene_symbol":"GSG1L2","gene_name":"GSG1 like 2 [Source:HGNC Symbol;Acc:HGNC:51826]","synonyms":null,"biotype":"protein_coding","ncbi_id":"644070","summary":null,"start":9802386,"end":9822071,"strand":-1,"description":"GSG1 like 2 [Source:HGNC Symbol;Acc:HGNC:51826]"}, {"versioned_ensembl_gene_id":"ENSG00000116455.13","gene_symbol":"WDR77","gene_name":"WD repeat domain 77 [Source:HGNC Symbol;Acc:HGNC:29652]","synonyms":"p44,MEP50","biotype":"protein_coding","ncbi_id":"79084","summary":"The protein encoded by this gene is an androgen receptor coactivator that forms a complex with protein arginine methyltransferase 5, which modifies specific arginines to dimethylarginines in several spliceosomal Sm proteins. The encoded protein may be involved in the early stages of prostate cancer, with most of the protein being nuclear-localized in benign cells but cytoplasmic in cancer cells. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":111439890,"end":111449376,"strand":-1,"description":"WD repeat domain 77 [Source:HGNC Symbol;Acc:HGNC:29652]"}, {"versioned_ensembl_gene_id":"ENSG00000223817.1","gene_symbol":"CDH23-AS1","gene_name":"CDH23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31433]","synonyms":"NCRNA00223,C10orf106,bA327E2.3","biotype":"antisense_RNA","ncbi_id":"102723377","summary":null,"start":71508153,"end":71511873,"strand":-1,"description":"CDH23 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31433]"}, {"versioned_ensembl_gene_id":"ENSG00000086200.16","gene_symbol":"IPO11","gene_name":"importin 11 [Source:HGNC Symbol;Acc:HGNC:20628]","synonyms":"RanBP11","biotype":"protein_coding","ncbi_id":"51194","summary":"Importins, including IPO11, are a members of the karyopherin/importin-beta family of transport receptors (see KPNB1; 602738) that mediate nucleocytoplasmic transport of protein and RNA cargoes (Plafker and Macara, 2000 [PubMed 11032817]).[supplied by OMIM, Sep 2008]","start":62403972,"end":62628582,"strand":1,"description":"importin 11 [Source:HGNC Symbol;Acc:HGNC:20628]"}, {"versioned_ensembl_gene_id":"ENSG00000230617.1","gene_symbol":"AC079987.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83424880,"end":83425002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278681.2","gene_symbol":"AC018558.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35435303,"end":35436341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000023191.16","gene_symbol":"RNH1","gene_name":"ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:10074]","synonyms":"RNH,RAI","biotype":"protein_coding","ncbi_id":"6050","summary":"Placental ribonuclease inhibitor (PRI) is a member of a family of proteinaceous cytoplasmic RNase inhibitors that occur in many tissues and bind to both intracellular and extracellular RNases (summarized by Lee et al., 1988 [PubMed 3219362]). In addition to control of intracellular RNases, the inhibitor may have a role in the regulation of angiogenin (MIM 105850). Ribonuclease inhibitor, of 50,000 Da, binds to ribonucleases and holds them in a latent form. Since neutral and alkaline ribonucleases probably play a critical role in the turnover of RNA in eukaryotic cells, RNH may be essential for control of mRNA turnover; the interaction of eukaryotic cells with ribonuclease may be reversible in vivo.[supplied by OMIM, Jul 2010]","start":494512,"end":507300,"strand":-1,"description":"ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:10074]"}, {"versioned_ensembl_gene_id":"ENSG00000152527.13","gene_symbol":"PLEKHH2","gene_name":"pleckstrin homology, MyTH4 and FERM domain containing H2 [Source:HGNC Symbol;Acc:HGNC:30506]","synonyms":"KIAA2028,PLEKHH1L","biotype":"protein_coding","ncbi_id":"130271","summary":null,"start":43637273,"end":43767987,"strand":1,"description":"pleckstrin homology, MyTH4 and FERM domain containing H2 [Source:HGNC Symbol;Acc:HGNC:30506]"}, {"versioned_ensembl_gene_id":"ENSG00000122507.20","gene_symbol":"BBS9","gene_name":"Bardet-Biedl syndrome 9 [Source:HGNC Symbol;Acc:HGNC:30000]","synonyms":"PTHB1,B1","biotype":"protein_coding","ncbi_id":"27241","summary":"This gene is downregulated by parathyroid hormone in osteoblastic cells, and therefore is thought to be involved in parathyroid hormone action in bones. The exact function of this gene has not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2017]","start":33129244,"end":33606068,"strand":1,"description":"Bardet-Biedl syndrome 9 [Source:HGNC Symbol;Acc:HGNC:30000]"}, {"versioned_ensembl_gene_id":"ENSG00000276691.1","gene_symbol":"AC004466.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47788426,"end":47788971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235214.1","gene_symbol":"FAM83C-AS1","gene_name":"FAM83C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16113]","synonyms":"NCRNA00154,dJ614O4.3,C20orf120","biotype":"antisense_RNA","ncbi_id":"140846","summary":null,"start":35285251,"end":35285756,"strand":1,"description":"FAM83C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:16113]"}, {"versioned_ensembl_gene_id":"ENSG00000023909.9","gene_symbol":"GCLM","gene_name":"glutamate-cysteine ligase modifier subunit [Source:HGNC Symbol;Acc:HGNC:4312]","synonyms":"GLCLR","biotype":"protein_coding","ncbi_id":"2730","summary":"Glutamate-cysteine ligase, also known as gamma-glutamylcysteine synthetase, is the first rate limiting enzyme of glutathione synthesis. The enzyme consists of two subunits, a heavy catalytic subunit and a light regulatory subunit. Gamma glutamylcysteine synthetase deficiency has been implicated in some forms of hemolytic anemia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":93885205,"end":93909456,"strand":-1,"description":"glutamate-cysteine ligase modifier subunit [Source:HGNC Symbol;Acc:HGNC:4312]"}, {"versioned_ensembl_gene_id":"ENSG00000153066.12","gene_symbol":"TXNDC11","gene_name":"thioredoxin domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28030]","synonyms":"EFP1","biotype":"protein_coding","ncbi_id":"51061","summary":null,"start":11679080,"end":11742878,"strand":-1,"description":"thioredoxin domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28030]"}, {"versioned_ensembl_gene_id":"ENSG00000258325.2","gene_symbol":"ITFG2-AS1","gene_name":"ITFG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53128]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283440","summary":null,"start":2796877,"end":2812902,"strand":-1,"description":"ITFG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53128]"}, {"versioned_ensembl_gene_id":"ENSG00000219392.1","gene_symbol":"ZNF602P","gene_name":"zinc finger protein 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:23313]","synonyms":"dJ265C24.5","biotype":"unprocessed_pseudogene","ncbi_id":"100419608","summary":null,"start":28115628,"end":28116551,"strand":1,"description":"zinc finger protein 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:23313]"}, {"versioned_ensembl_gene_id":"ENSG00000256902.1","gene_symbol":"IQSEC3P1","gene_name":"IQ motif and Sec7 domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49848]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132450","summary":null,"start":2752597,"end":2753132,"strand":-1,"description":"IQ motif and Sec7 domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49848]"}, {"versioned_ensembl_gene_id":"ENSG00000131652.13","gene_symbol":"THOC6","gene_name":"THO complex 6 [Source:HGNC Symbol;Acc:HGNC:28369]","synonyms":"MGC2655,fSAP35,WDR58","biotype":"protein_coding","ncbi_id":"79228","summary":"This gene encodes a subunit of the multi-protein THO complex, which is involved in coordination between transcription and mRNA processing. The THO complex is a component of the TREX (transcription/export) complex, which is involved in transcription and export of mRNAs. A missense mutation in this gene is associated with a neurodevelopmental disorder called Beaulieu-Boycott-Innes syndrome. [provided by RefSeq, Dec 2016]","start":3024027,"end":3027755,"strand":1,"description":"THO complex 6 [Source:HGNC Symbol;Acc:HGNC:28369]"}, {"versioned_ensembl_gene_id":"ENSG00000270552.1","gene_symbol":"DUXAP3","gene_name":"double homeobox A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32182]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"503632","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":42747544,"end":42748687,"strand":-1,"description":"double homeobox A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:32182]"}, {"versioned_ensembl_gene_id":"ENSG00000203648.3","gene_symbol":"AC007618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2659937,"end":2660969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267639.3","gene_symbol":"AC073135.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":198219890,"end":198222703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167995.15","gene_symbol":"BEST1","gene_name":"bestrophin 1 [Source:HGNC Symbol;Acc:HGNC:12703]","synonyms":"VMD2,RP50,BMD,BEST","biotype":"protein_coding","ncbi_id":"7439","summary":"This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008]","start":61949821,"end":61965515,"strand":1,"description":"bestrophin 1 [Source:HGNC Symbol;Acc:HGNC:12703]"}, {"versioned_ensembl_gene_id":"ENSG00000157191.19","gene_symbol":"NECAP2","gene_name":"NECAP endocytosis associated 2 [Source:HGNC Symbol;Acc:HGNC:25528]","synonyms":"FLJ10420","biotype":"protein_coding","ncbi_id":"55707","summary":"This gene likely encodes a member of the adaptin-ear-binding coat-associated protein family. Studies of a similar protein in rat suggest a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":16440672,"end":16460078,"strand":1,"description":"NECAP endocytosis associated 2 [Source:HGNC Symbol;Acc:HGNC:25528]"}, {"versioned_ensembl_gene_id":"ENSG00000229497.1","gene_symbol":"AC005189.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43767290,"end":43767599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156697.12","gene_symbol":"UTP14A","gene_name":"UTP14A, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:10665]","synonyms":"Utp14,SDCCAG16,NY-CO-16","biotype":"protein_coding","ncbi_id":"10813","summary":"This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. An autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":129906121,"end":129929761,"strand":1,"description":"UTP14A, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:10665]"}, {"versioned_ensembl_gene_id":"ENSG00000274679.4","gene_symbol":"SPATC1L","gene_name":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]","synonyms":"C21orf56","biotype":"protein_coding","ncbi_id":"84221","summary":null,"start":46161526,"end":46186787,"strand":-1,"description":"spermatogenesis and centriole associated 1 like [Source:HGNC Symbol;Acc:HGNC:1298]"}, {"versioned_ensembl_gene_id":"ENSG00000122779.17","gene_symbol":"TRIM24","gene_name":"tripartite motif containing 24 [Source:HGNC Symbol;Acc:HGNC:11812]","synonyms":"Tif1a,TIF1,RNF82,hTIF1","biotype":"protein_coding","ncbi_id":"8805","summary":"The protein encoded by this gene mediates transcriptional control by interaction with the activation function 2 (AF2) region of several nuclear receptors, including the estrogen, retinoic acid, and vitamin D3 receptors. The protein localizes to nuclear bodies and is thought to associate with chromatin and heterochromatin-associated factors. The protein is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains - a RING, a B-box type 1 and a B-box type 2 - and a coiled-coil region. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":138460334,"end":138589993,"strand":1,"description":"tripartite motif containing 24 [Source:HGNC Symbol;Acc:HGNC:11812]"}, {"versioned_ensembl_gene_id":"ENSG00000234995.1","gene_symbol":"AC013429.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138490581,"end":138491361,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197993.7","gene_symbol":"KEL","gene_name":"Kell blood group, metallo-endopeptidase [Source:HGNC Symbol;Acc:HGNC:6308]","synonyms":"ECE3,CD238","biotype":"protein_coding","ncbi_id":"3792","summary":"This gene encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen. The Kell glycoprotein links via a single disulfide bond to the XK membrane protein that carries the Kx antigen. The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases. [provided by RefSeq, Jul 2008]","start":142941114,"end":142962681,"strand":-1,"description":"Kell blood group, metallo-endopeptidase [Source:HGNC Symbol;Acc:HGNC:6308]"}, {"versioned_ensembl_gene_id":"ENSG00000138411.10","gene_symbol":"HECW2","gene_name":"HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:29853]","synonyms":"NEDL2,KIAA1301","biotype":"protein_coding","ncbi_id":"57520","summary":"This gene encodes a member of a family of E3 ubiquitin ligases which plays an important role in the proliferation, migration and differentiation of neural crest cells as a regulator of glial cell line-derived neurotrophic factor (GDNF)/Ret signaling. This gene also plays an important role in angiogenesis through stabilization of endothelial cell-to-cell junctions as a regulator of angiomotin-like 1 stability. The encoded protein contains an N-terminal calcium/lipid-binding (C2) domain involved in membrane targeting, two-four WW domains responsible for cellular localization and substrate recognition, and a C-terminal homologous with E6-associated protein C-terminus (HECT) catalytic domain. Naturally occurring mutations in this gene are associated with neurodevelopmental delay, hypotonia, and epilepsy. The decreased expression of this gene in the aganglionic colon is associated with Hirschsprung's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":196194370,"end":196593692,"strand":-1,"description":"HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:29853]"}, {"versioned_ensembl_gene_id":"ENSG00000231556.1","gene_symbol":"RSL24D1P3","gene_name":"ribosomal L24 domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37883]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130721","summary":null,"start":65335174,"end":65335668,"strand":-1,"description":"ribosomal L24 domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37883]"}, {"versioned_ensembl_gene_id":"ENSG00000138593.8","gene_symbol":"SECISBP2L","gene_name":"SECIS binding protein 2 like [Source:HGNC Symbol;Acc:HGNC:28997]","synonyms":"KIAA0256","biotype":"protein_coding","ncbi_id":"9728","summary":null,"start":48988476,"end":49046563,"strand":-1,"description":"SECIS binding protein 2 like [Source:HGNC Symbol;Acc:HGNC:28997]"}, {"versioned_ensembl_gene_id":"ENSG00000229056.2","gene_symbol":"AC020571.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":196260024,"end":196264204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219891.2","gene_symbol":"ZSCAN12P1","gene_name":"zinc finger and SCAN domain containing 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13850]","synonyms":"ZSCAN12L1,ZNF96P1,ZNF96L1,ZNF305P1,ZNF187p1,dJ313I6.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"221584","summary":null,"start":28091154,"end":28093664,"strand":1,"description":"zinc finger and SCAN domain containing 12 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13850]"}, {"versioned_ensembl_gene_id":"ENSG00000135945.9","gene_symbol":"REV1","gene_name":"REV1, DNA directed polymerase [Source:HGNC Symbol;Acc:HGNC:14060]","synonyms":"REV1L","biotype":"protein_coding","ncbi_id":"51455","summary":"This gene encodes a protein with similarity to the S. cerevisiae mutagenesis protein Rev1. The Rev1 proteins contain a BRCT domain, which is important in protein-protein interactions. A suggested role for the human Rev1-like protein is as a scaffold that recruits DNA polymerases involved in translesion synthesis (TLS) of damaged DNA. [provided by RefSeq, Mar 2016]","start":99400475,"end":99490035,"strand":-1,"description":"REV1, DNA directed polymerase [Source:HGNC Symbol;Acc:HGNC:14060]"}, {"versioned_ensembl_gene_id":"ENSG00000230787.1","gene_symbol":"PSAT1P3","gene_name":"phosphoserine aminotransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43989]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729779","summary":null,"start":79054945,"end":79056055,"strand":-1,"description":"phosphoserine aminotransferase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43989]"}, {"versioned_ensembl_gene_id":"ENSG00000197279.3","gene_symbol":"ZNF165","gene_name":"zinc finger protein 165 [Source:HGNC Symbol;Acc:HGNC:12953]","synonyms":"ZSCAN7,CT53","biotype":"protein_coding","ncbi_id":"7718","summary":"This gene encodes a member of the Kruppel family of zinc finger proteins. Members of this DNA-binding protein family act as transcriptional regulators. This gene is located within a cluster of zinc finger family members. The encoded protein may play a role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":28080975,"end":28089563,"strand":1,"description":"zinc finger protein 165 [Source:HGNC Symbol;Acc:HGNC:12953]"}, {"versioned_ensembl_gene_id":"ENSG00000260555.1","gene_symbol":"AC092681.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":150000752,"end":150005124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153064.11","gene_symbol":"BANK1","gene_name":"B-cell scaffold protein with ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:18233]","synonyms":"FLJ20706,BANK","biotype":"protein_coding","ncbi_id":"55024","summary":"The protein encoded by this gene is a B-cell-specific scaffold protein that functions in B-cell receptor-induced calcium mobilization from intracellular stores. This protein can also promote Lyn-mediated tyrosine phosphorylation of inositol 1,4,5-trisphosphate receptors. Polymorphisms in this gene are associated with susceptibility to systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":101411286,"end":102074812,"strand":1,"description":"B-cell scaffold protein with ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:18233]"}, {"versioned_ensembl_gene_id":"ENSG00000251149.1","gene_symbol":"MTND5P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42307]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873201","summary":null,"start":101972423,"end":101972798,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42307]"}, {"versioned_ensembl_gene_id":"ENSG00000107779.13","gene_symbol":"BMPR1A","gene_name":"bone morphogenetic protein receptor type 1A [Source:HGNC Symbol;Acc:HGNC:1076]","synonyms":"CD292,ALK3,ACVRLK3","biotype":"protein_coding","ncbi_id":"657","summary":"The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine/threonine kinases that include the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. These receptors are also closely related to the activin receptors, ACVR1 and ACVR2. The ligands of these receptors are members of the TGF-beta superfamily. TGF-betas and activins transduce their signals through the formation of heteromeric complexes with 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. [provided by RefSeq, Jul 2008]","start":86756601,"end":86932838,"strand":1,"description":"bone morphogenetic protein receptor type 1A [Source:HGNC Symbol;Acc:HGNC:1076]"}, {"versioned_ensembl_gene_id":"ENSG00000163468.14","gene_symbol":"CCT3","gene_name":"chaperonin containing TCP1 subunit 3 [Source:HGNC Symbol;Acc:HGNC:1616]","synonyms":"TRIC5,Cctg","biotype":"protein_coding","ncbi_id":"7203","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternate transcriptional splice variants have been characterized for this gene. In addition, a pseudogene of this gene has been found on chromosome 8. [provided by RefSeq, Aug 2010]","start":156308968,"end":156367873,"strand":-1,"description":"chaperonin containing TCP1 subunit 3 [Source:HGNC Symbol;Acc:HGNC:1616]"}, {"versioned_ensembl_gene_id":"ENSG00000106013.14","gene_symbol":"ANKRD7","gene_name":"ankyrin repeat domain 7 [Source:HGNC Symbol;Acc:HGNC:18588]","synonyms":"TSA806","biotype":"protein_coding","ncbi_id":"56311","summary":null,"start":118214669,"end":118496171,"strand":1,"description":"ankyrin repeat domain 7 [Source:HGNC Symbol;Acc:HGNC:18588]"}, {"versioned_ensembl_gene_id":"ENSG00000234441.1","gene_symbol":"AC105272.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":103668071,"end":103668268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270492.1","gene_symbol":"AC137695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129334586,"end":129335074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259889.1","gene_symbol":"AC093802.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239734956,"end":239735538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220256.3","gene_symbol":"AC093802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239762860,"end":239802883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205100.2","gene_symbol":"HSP90AA4P","gene_name":"heat shock protein 90 alpha family class A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:5255]","synonyms":"HSPCAL2","biotype":"transcribed_processed_pseudogene","ncbi_id":"3323","summary":null,"start":189472965,"end":189475192,"strand":1,"description":"heat shock protein 90 alpha family class A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:5255]"}, {"versioned_ensembl_gene_id":"ENSG00000249877.1","gene_symbol":"AC105924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189288677,"end":189291336,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278243.2","gene_symbol":"TSTA3","gene_name":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]","synonyms":"SDR4E1,P35B,FX","biotype":"protein_coding","ncbi_id":"7264","summary":"Tissue specific transplantation antigen P35B is a NADP(H)-binding protein. It catalyze the two-step epimerase and the reductase reactions in GDP-D-mannose metabolism, converting GDP-4-keto-6-D-deoxymannose to GDP-L-fucose. GDP-L-fucose is the substrate of several fucosyltransferases involved in the expression of many glycoconjugates, including blood group ABH antigens and developmental adhesion antigens. Mutations in this gene may cause leukocyte adhesion deficiency, type II. [provided by RefSeq, Jul 2008]","start":143612618,"end":143618048,"strand":-1,"description":"tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:HGNC:12390]"}, {"versioned_ensembl_gene_id":"ENSG00000258038.5","gene_symbol":"LINC02327","gene_name":"long intergenic non-protein coding RNA 2327 [Source:HGNC Symbol;Acc:HGNC:53247]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724917","summary":null,"start":28830244,"end":28968400,"strand":1,"description":"long intergenic non-protein coding RNA 2327 [Source:HGNC Symbol;Acc:HGNC:53247]"}, {"versioned_ensembl_gene_id":"ENSG00000228601.1","gene_symbol":"AL121914.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56459428,"end":56459583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232109.1","gene_symbol":"VN1R54P","gene_name":"vomeronasal 1 receptor 54 pseudogene [Source:HGNC Symbol;Acc:HGNC:37374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312807","summary":null,"start":42660728,"end":42661776,"strand":1,"description":"vomeronasal 1 receptor 54 pseudogene [Source:HGNC Symbol;Acc:HGNC:37374]"}, {"versioned_ensembl_gene_id":"ENSG00000229932.3","gene_symbol":"YWHAZP3","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31101]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"143371","summary":null,"start":23136924,"end":23137661,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31101]"}, {"versioned_ensembl_gene_id":"ENSG00000263438.5","gene_symbol":"LINC01919","gene_name":"long intergenic non-protein coding RNA 1919 [Source:HGNC Symbol;Acc:HGNC:52739]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724651","summary":null,"start":53568447,"end":53597851,"strand":1,"description":"long intergenic non-protein coding RNA 1919 [Source:HGNC Symbol;Acc:HGNC:52739]"}, {"versioned_ensembl_gene_id":"ENSG00000125850.10","gene_symbol":"OVOL2","gene_name":"ovo like zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:15804]","synonyms":"bA504H3.3,ZNF339,HOVO2,CHED1,CHED","biotype":"protein_coding","ncbi_id":"58495","summary":"This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016]","start":17956979,"end":18059188,"strand":-1,"description":"ovo like zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:15804]"}, {"versioned_ensembl_gene_id":"ENSG00000218902.3","gene_symbol":"PTMAP3","gene_name":"prothymosin, alpha pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9626]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"5760","summary":null,"start":18011955,"end":18012284,"strand":1,"description":"prothymosin, alpha pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:9626]"}, {"versioned_ensembl_gene_id":"ENSG00000227124.8","gene_symbol":"ZNF717","gene_name":"zinc finger protein 717 [Source:HGNC Symbol;Acc:HGNC:29448]","synonyms":"ZNF838,X17","biotype":"protein_coding","ncbi_id":"100131827","summary":"This gene encodes a Kruppel-associated box (KRAB) zinc-finger protein, which belongs to a large group of transcriptional regulators in mammals. These proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation and apoptosis, and in regulating viral replication and transcription. A pseudogene of this gene was identified on chromosome 1. [provided by RefSeq, May 2016]","start":75709643,"end":75785583,"strand":-1,"description":"zinc finger protein 717 [Source:HGNC Symbol;Acc:HGNC:29448]"}, {"versioned_ensembl_gene_id":"ENSG00000197182.14","gene_symbol":"MIRLET7BHG","gene_name":"MIRLET7B host gene [Source:HGNC Symbol;Acc:HGNC:37189]","synonyms":"linc-Ppara","biotype":"lincRNA","ncbi_id":"400931","summary":null,"start":46053869,"end":46113928,"strand":1,"description":"MIRLET7B host gene [Source:HGNC Symbol;Acc:HGNC:37189]"}, {"versioned_ensembl_gene_id":"ENSG00000099899.14","gene_symbol":"TRMT2A","gene_name":"tRNA methyltransferase 2 homolog A [Source:HGNC Symbol;Acc:HGNC:24974]","synonyms":"HTF9C","biotype":"protein_coding","ncbi_id":"27037","summary":"The protein encoded by this gene is of unknown function. However, it is orthologous to the mouse Trmt2a gene and contains an RNA methyltransferase domain. Expression of this gene varies during the cell cycle, with aberrant expression being a possible biomarker in certain breast cancers. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":20111866,"end":20117392,"strand":-1,"description":"tRNA methyltransferase 2 homolog A [Source:HGNC Symbol;Acc:HGNC:24974]"}, {"versioned_ensembl_gene_id":"ENSG00000184486.9","gene_symbol":"POU3F2","gene_name":"POU class 3 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9215]","synonyms":"POUF3,OTF7,OCT7,BRN2","biotype":"protein_coding","ncbi_id":"5454","summary":"This gene encodes a member of the POU-III class of neural transcription factors. The encoded protein is involved in neuronal differentiation and enhances the activation of corticotropin-releasing hormone regulated genes. Overexpression of this protein is associated with an increase in the proliferation of melanoma cells. [provided by RefSeq, Mar 2012]","start":98834592,"end":98839470,"strand":1,"description":"POU class 3 homeobox 2 [Source:HGNC Symbol;Acc:HGNC:9215]"}, {"versioned_ensembl_gene_id":"ENSG00000283010.1","gene_symbol":"AL589826.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98829967,"end":98832508,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103540.16","gene_symbol":"CCP110","gene_name":"centriolar coiled-coil protein 110 [Source:HGNC Symbol;Acc:HGNC:24342]","synonyms":"KIAA0419,CP110","biotype":"protein_coding","ncbi_id":"9738","summary":null,"start":19523811,"end":19553408,"strand":1,"description":"centriolar coiled-coil protein 110 [Source:HGNC Symbol;Acc:HGNC:24342]"}, {"versioned_ensembl_gene_id":"ENSG00000158296.13","gene_symbol":"SLC13A3","gene_name":"solute carrier family 13 member 3 [Source:HGNC Symbol;Acc:HGNC:14430]","synonyms":"SDCT2,NADC3","biotype":"protein_coding","ncbi_id":"64849","summary":"Mammalian sodium-dicarboxylate cotransporters transport succinate and other Krebs cycle intermediates. They fall into 2 categories based on their substrate affinity: low affinity and high affinity. Both the low- and high-affinity transporters play an important role in the handling of citrate by the kidneys. The protein encoded by this gene represents the high-affinity form. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, although the full-length nature of some of them have not been characterized yet. [provided by RefSeq, Jul 2008]","start":46557823,"end":46684467,"strand":-1,"description":"solute carrier family 13 member 3 [Source:HGNC Symbol;Acc:HGNC:14430]"}, {"versioned_ensembl_gene_id":"ENSG00000187472.4","gene_symbol":"AL589826.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98780257,"end":98780505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137040.9","gene_symbol":"RANBP6","gene_name":"RAN binding protein 6 [Source:HGNC Symbol;Acc:HGNC:9851]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26953","summary":null,"start":6011043,"end":6015625,"strand":-1,"description":"RAN binding protein 6 [Source:HGNC Symbol;Acc:HGNC:9851]"}, {"versioned_ensembl_gene_id":"ENSG00000280181.1","gene_symbol":"AC025262.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":64709458,"end":64710513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243762.1","gene_symbol":"AC006547.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20110821,"end":20111875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204982.3","gene_symbol":"PRSS3P4","gene_name":"protease, serine 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43789]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480774","summary":null,"start":33613848,"end":33614009,"strand":-1,"description":"protease, serine 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43789]"}, {"versioned_ensembl_gene_id":"ENSG00000279467.1","gene_symbol":"AP000350.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23865248,"end":23873277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233870.1","gene_symbol":"AC007881.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71178587,"end":71178773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244953.1","gene_symbol":"AC087521.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43943787,"end":43947206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128534.7","gene_symbol":"LSM8","gene_name":"LSM8 homolog, U6 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:20471]","synonyms":"YJR022W","biotype":"protein_coding","ncbi_id":"51691","summary":"This gene encodes a member of the like-Sm family of proteins. The encoded protein consists of a closed barrel shape, made up of five anti-parallel beta strands and an alpha helix. This protein partners with six paralogs to form a heteroheptameric ring which transiently binds U6 small nuclear RNAs and is involved in the general maturation of RNA in the nucleus. [provided by RefSeq, Jan 2010]","start":118184032,"end":118192824,"strand":1,"description":"LSM8 homolog, U6 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:20471]"}, {"versioned_ensembl_gene_id":"ENSG00000257086.1","gene_symbol":"AP001453.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64246939,"end":64249494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254409.1","gene_symbol":"AC087521.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":43921059,"end":44001157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187479.5","gene_symbol":"C11orf96","gene_name":"chromosome 11 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:38675]","synonyms":"AG2","biotype":"protein_coding","ncbi_id":"387763","summary":null,"start":43925342,"end":43944338,"strand":1,"description":"chromosome 11 open reading frame 96 [Source:HGNC Symbol;Acc:HGNC:38675]"}, {"versioned_ensembl_gene_id":"ENSG00000258727.1","gene_symbol":"AL135999.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23561097,"end":23568073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164669.13","gene_symbol":"INTS4P1","gene_name":"integrator complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21925]","synonyms":"INTS4L1,FLJ25037","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285905","summary":null,"start":65141032,"end":65234216,"strand":1,"description":"integrator complex subunit 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21925]"}, {"versioned_ensembl_gene_id":"ENSG00000186960.10","gene_symbol":"LINC01551","gene_name":"long intergenic non-protein coding RNA 1551 [Source:HGNC Symbol;Acc:HGNC:19828]","synonyms":"C14orf23","biotype":"lincRNA","ncbi_id":"387978","summary":null,"start":28772704,"end":28813453,"strand":1,"description":"long intergenic non-protein coding RNA 1551 [Source:HGNC Symbol;Acc:HGNC:19828]"}, {"versioned_ensembl_gene_id":"ENSG00000061273.17","gene_symbol":"HDAC7","gene_name":"histone deacetylase 7 [Source:HGNC Symbol;Acc:HGNC:14067]","synonyms":"DKFZP586J0917,HDAC7A","biotype":"protein_coding","ncbi_id":"51564","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene has sequence homology to members of the histone deacetylase family. This gene is orthologous to mouse HDAC7 gene whose protein promotes repression mediated via the transcriptional corepressor SMRT. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":47782722,"end":47833132,"strand":-1,"description":"histone deacetylase 7 [Source:HGNC Symbol;Acc:HGNC:14067]"}, {"versioned_ensembl_gene_id":"ENSG00000235669.1","gene_symbol":"AC004593.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29199540,"end":29208970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103460.16","gene_symbol":"TOX3","gene_name":"TOX high mobility group box family member 3 [Source:HGNC Symbol;Acc:HGNC:11972]","synonyms":"TNRC9,CAGF9","biotype":"protein_coding","ncbi_id":"27324","summary":"The protein encoded by this gene contains an HMG-box, indicating that it may be involved in bending and unwinding of DNA and alteration of chromatin structure. The C-terminus of the encoded protein is glutamine-rich due to CAG repeats in the coding sequence. A minor allele of this gene has been implicated in an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2009]","start":52438005,"end":52547802,"strand":-1,"description":"TOX high mobility group box family member 3 [Source:HGNC Symbol;Acc:HGNC:11972]"}, {"versioned_ensembl_gene_id":"ENSG00000184897.5","gene_symbol":"H1FX","gene_name":"H1 histone family member X [Source:HGNC Symbol;Acc:HGNC:4722]","synonyms":"MGC8350,MGC15959,H1X","biotype":"protein_coding","ncbi_id":"8971","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H1 family. [provided by RefSeq, Oct 2015]","start":129314771,"end":129316277,"strand":-1,"description":"H1 histone family member X [Source:HGNC Symbol;Acc:HGNC:4722]"}, {"versioned_ensembl_gene_id":"ENSG00000239453.1","gene_symbol":"SIDT1-AS1","gene_name":"SIDT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41126]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874030","summary":null,"start":113588748,"end":113590189,"strand":-1,"description":"SIDT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41126]"}, {"versioned_ensembl_gene_id":"ENSG00000232420.2","gene_symbol":"IL9RP2","gene_name":"interleukin 9 receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6032]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"439945","summary":null,"start":80394,"end":86265,"strand":-1,"description":"interleukin 9 receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6032]"}, {"versioned_ensembl_gene_id":"ENSG00000111276.10","gene_symbol":"CDKN1B","gene_name":"cyclin dependent kinase inhibitor 1B [Source:HGNC Symbol;Acc:HGNC:1785]","synonyms":"P27KIP1,KIP1","biotype":"protein_coding","ncbi_id":"1027","summary":"This gene encodes a cyclin-dependent kinase inhibitor, which shares a limited similarity with CDK inhibitor CDKN1A/p21. The encoded protein binds to and prevents the activation of cyclin E-CDK2 or cyclin D-CDK4 complexes, and thus controls the cell cycle progression at G1. The degradation of this protein, which is triggered by its CDK dependent phosphorylation and subsequent ubiquitination by SCF complexes, is required for the cellular transition from quiescence to the proliferative state. Mutations in this gene are associated with multiple endocrine neoplasia type IV (MEN4). [provided by RefSeq, Apr 2014]","start":12715058,"end":12722371,"strand":1,"description":"cyclin dependent kinase inhibitor 1B [Source:HGNC Symbol;Acc:HGNC:1785]"}, {"versioned_ensembl_gene_id":"ENSG00000282790.1","gene_symbol":"AC068400.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37412556,"end":37413214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261689.1","gene_symbol":"AGGF1P4","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38054]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129351","summary":null,"start":35389203,"end":35390003,"strand":-1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38054]"}, {"versioned_ensembl_gene_id":"ENSG00000230419.1","gene_symbol":"AL845454.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878575,"end":29879543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231279.2","gene_symbol":"AL662857.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29287419,"end":29288361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244459.2","gene_symbol":"AC147067.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1574062,"end":1580253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228414.6","gene_symbol":"LINC01185","gene_name":"long intergenic non-protein coding RNA 1185 [Source:HGNC Symbol;Acc:HGNC:49572]","synonyms":"FLJ16341","biotype":"lincRNA","ncbi_id":"400957","summary":null,"start":60825132,"end":60881314,"strand":-1,"description":"long intergenic non-protein coding RNA 1185 [Source:HGNC Symbol;Acc:HGNC:49572]"}, {"versioned_ensembl_gene_id":"ENSG00000235608.1","gene_symbol":"NKX1-1","gene_name":"NK1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:24975]","synonyms":"SAX2,HSPX153","biotype":"protein_coding","ncbi_id":"54729","summary":"This gene encodes a transcription factor that belongs to NKX family of homeodomain-containing proteins which are critical regulators of organ development. In mice, the orthologous gene is expressed predominantly in the brainstem, in the vicinity of serotonergic neurons, and is required for the coordinated crosstalk of factors involved in the maintenance of energy homeostasis. Mice with a knockout of the orthologous gene lack subcutaneous fat and intra-abdominal epididymal and mesenteric white adipose tissue two weeks after birth, and die within three weeks after birth. [provided by RefSeq, Jul 2017]","start":1402932,"end":1406331,"strand":-1,"description":"NK1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:24975]"}, {"versioned_ensembl_gene_id":"ENSG00000213194.3","gene_symbol":"CDK7P1","gene_name":"cyclin dependent kinase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18614]","synonyms":"CDK7PS","biotype":"processed_pseudogene","ncbi_id":"220786","summary":null,"start":157210847,"end":157211539,"strand":-1,"description":"cyclin dependent kinase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18614]"}, {"versioned_ensembl_gene_id":"ENSG00000144619.14","gene_symbol":"CNTN4","gene_name":"contactin 4 [Source:HGNC Symbol;Acc:HGNC:2174]","synonyms":"BIG-2","biotype":"protein_coding","ncbi_id":"152330","summary":"This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]","start":2098813,"end":3057956,"strand":1,"description":"contactin 4 [Source:HGNC Symbol;Acc:HGNC:2174]"}, {"versioned_ensembl_gene_id":"ENSG00000183022.5","gene_symbol":"TPM3P8","gene_name":"tropomyosin 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39171]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646839","summary":null,"start":230573167,"end":230573809,"strand":-1,"description":"tropomyosin 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39171]"}, {"versioned_ensembl_gene_id":"ENSG00000260934.1","gene_symbol":"AC130456.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19501689,"end":19502286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150753.11","gene_symbol":"CCT5","gene_name":"chaperonin containing TCP1 subunit 5 [Source:HGNC Symbol;Acc:HGNC:1618]","synonyms":"KIAA0098","biotype":"protein_coding","ncbi_id":"22948","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP). Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 5 and 13. [provided by RefSeq, Apr 2015]","start":10249921,"end":10266412,"strand":1,"description":"chaperonin containing TCP1 subunit 5 [Source:HGNC Symbol;Acc:HGNC:1618]"}, {"versioned_ensembl_gene_id":"ENSG00000227089.2","gene_symbol":"AL031767.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21354411,"end":21355296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233625.1","gene_symbol":"AL035045.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17887363,"end":17888160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275963.1","gene_symbol":"AC008115.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12648939,"end":12649713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111727.11","gene_symbol":"HCFC2","gene_name":"host cell factor C2 [Source:HGNC Symbol;Acc:HGNC:24972]","synonyms":"HCF-2","biotype":"protein_coding","ncbi_id":"29915","summary":"This gene encodes one of two proteins which interact with VP16, a herpes simplex virus protein that initiates virus infection. Both the encoded protein and the original Herpes host cell factor interact with VP16 through a beta-propeller domain. The original Herpes host cell factor, however, is effective at initiating viral infection while the encoded protein is not. Transcripts of varying length due to alternative polyadenylation signals have been described. [provided by RefSeq, Jul 2008]","start":104064457,"end":104106524,"strand":1,"description":"host cell factor C2 [Source:HGNC Symbol;Acc:HGNC:24972]"}, {"versioned_ensembl_gene_id":"ENSG00000226233.1","gene_symbol":"Z82188.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37215738,"end":37215891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241532.1","gene_symbol":"AGGF1P3","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38053]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391552","summary":null,"start":75653561,"end":75654773,"strand":-1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38053]"}, {"versioned_ensembl_gene_id":"ENSG00000241622.1","gene_symbol":"RARRES2P1","gene_name":"retinoic acid receptor responder 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48700]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643255","summary":null,"start":75658534,"end":75659014,"strand":1,"description":"retinoic acid receptor responder 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48700]"}, {"versioned_ensembl_gene_id":"ENSG00000279427.1","gene_symbol":"AC007490.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52436772,"end":52437474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215785.2","gene_symbol":"CFL1P6","gene_name":"cofilin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34545]","synonyms":"CFLP6","biotype":"processed_pseudogene","ncbi_id":"390996","summary":null,"start":10990978,"end":10991797,"strand":-1,"description":"cofilin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:34545]"}, {"versioned_ensembl_gene_id":"ENSG00000211643.2","gene_symbol":"IGLV5-52","gene_name":"immunoglobulin lambda variable 5-52 [Source:HGNC Symbol;Acc:HGNC:5926]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28779","summary":null,"start":22318727,"end":22319226,"strand":1,"description":"immunoglobulin lambda variable 5-52 [Source:HGNC Symbol;Acc:HGNC:5926]"}, {"versioned_ensembl_gene_id":"ENSG00000274422.1","gene_symbol":"AC245060.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22283928,"end":22287220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172971.7","gene_symbol":"UNC93B3","gene_name":"unc-93 homolog B3 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13483]","synonyms":"UNC93B3P","biotype":"unprocessed_pseudogene","ncbi_id":"285296","summary":null,"start":75619506,"end":75623849,"strand":-1,"description":"unc-93 homolog B3 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13483]"}, {"versioned_ensembl_gene_id":"ENSG00000215311.3","gene_symbol":"NPM1P12","gene_name":"nucleophosmin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:7914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10835","summary":null,"start":149334024,"end":149334857,"strand":1,"description":"nucleophosmin 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:7914]"}, {"versioned_ensembl_gene_id":"ENSG00000223419.1","gene_symbol":"AC006022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30742431,"end":30742818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142661.18","gene_symbol":"MYOM3","gene_name":"myomesin 3 [Source:HGNC Symbol;Acc:HGNC:26679]","synonyms":"FLJ35961","biotype":"protein_coding","ncbi_id":"127294","summary":null,"start":24056035,"end":24112175,"strand":-1,"description":"myomesin 3 [Source:HGNC Symbol;Acc:HGNC:26679]"}, {"versioned_ensembl_gene_id":"ENSG00000143437.20","gene_symbol":"ARNT","gene_name":"aryl hydrocarbon receptor nuclear translocator [Source:HGNC Symbol;Acc:HGNC:700]","synonyms":"HIF-1beta,bHLHe2","biotype":"protein_coding","ncbi_id":"405","summary":"This gene encodes a protein containing a basic helix-loop-helix domain and two characteristic PAS domains along with a PAC domain. The encoded protein binds to ligand-bound aryl hydrocarbon receptor and aids in the movement of this complex to the nucleus, where it promotes the expression of genes involved in xenobiotic metabolism. This protein is also a co-factor for transcriptional regulation by hypoxia-inducible factor 1. Chromosomal translocation of this locus with the ETV6 (ets variant 6) gene on chromosome 12 have been described in leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2013]","start":150809705,"end":150876768,"strand":-1,"description":"aryl hydrocarbon receptor nuclear translocator [Source:HGNC Symbol;Acc:HGNC:700]"}, {"versioned_ensembl_gene_id":"ENSG00000234293.1","gene_symbol":"BACH1-IT3","gene_name":"BACH1 intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:16455]","synonyms":"C21orf8","biotype":"sense_intronic","ncbi_id":"54147","summary":null,"start":29496047,"end":29500386,"strand":1,"description":"BACH1 intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:16455]"}, {"versioned_ensembl_gene_id":"ENSG00000226103.2","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"D6S53E,G4","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31649040,"end":31651514,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000233221.6","gene_symbol":"AC133785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130830978,"end":130836994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225189.1","gene_symbol":"REREP1Y","gene_name":"arginine-glutamic acid dipeptide repeats pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:38795]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105377240","summary":null,"start":23462465,"end":23472280,"strand":1,"description":"arginine-glutamic acid dipeptide repeats pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:38795]"}, {"versioned_ensembl_gene_id":"ENSG00000229230.3","gene_symbol":"MT1P3","gene_name":"metallothionein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16120]","synonyms":"MTL4,dJ614O4.6,C20orf127","biotype":"processed_pseudogene","ncbi_id":"140851","summary":null,"start":35218009,"end":35218185,"strand":1,"description":"metallothionein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16120]"}, {"versioned_ensembl_gene_id":"ENSG00000260327.2","gene_symbol":"ACTR3BP3","gene_name":"ACTR3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38678]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647156","summary":null,"start":32379071,"end":32380049,"strand":-1,"description":"ACTR3B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38678]"}, {"versioned_ensembl_gene_id":"ENSG00000240424.2","gene_symbol":"AC092824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12568201,"end":12568776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108064.10","gene_symbol":"TFAM","gene_name":"transcription factor A, mitochondrial [Source:HGNC Symbol;Acc:HGNC:11741]","synonyms":"TCF6L2,TCF6","biotype":"protein_coding","ncbi_id":"7019","summary":"This gene encodes a key mitochondrial transcription factor containing two high mobility group motifs. The encoded protein also functions in mitochondrial DNA replication and repair. Sequence polymorphisms in this gene are associated with Alzheimer's and Parkinson's diseases. There are pseudogenes for this gene on chromosomes 6, 7, and 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":58385022,"end":58399221,"strand":1,"description":"transcription factor A, mitochondrial [Source:HGNC Symbol;Acc:HGNC:11741]"}, {"versioned_ensembl_gene_id":"ENSG00000153071.14","gene_symbol":"DAB2","gene_name":"DAB2, clathrin adaptor protein [Source:HGNC Symbol;Acc:HGNC:2662]","synonyms":"DOC-2","biotype":"protein_coding","ncbi_id":"1601","summary":"This gene encodes a mitogen-responsive phosphoprotein. It is expressed in normal ovarian epithelial cells, but is down-regulated or absent from ovarian carcinoma cell lines, suggesting its role as a tumor suppressor. This protein binds to the SH3 domains of GRB2, an adaptor protein that couples tyrosine kinase receptors to SOS (a guanine nucleotide exchange factor for Ras), via its C-terminal proline-rich sequences, and may thus modulate growth factor/Ras pathways by competing with SOS for binding to GRB2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":39371675,"end":39462300,"strand":-1,"description":"DAB2, clathrin adaptor protein [Source:HGNC Symbol;Acc:HGNC:2662]"}, {"versioned_ensembl_gene_id":"ENSG00000241168.1","gene_symbol":"AC128685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":163026396,"end":163232149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053328.8","gene_symbol":"METTL24","gene_name":"methyltransferase like 24 [Source:HGNC Symbol;Acc:HGNC:21566]","synonyms":"dJ71D21.2,C6orf186","biotype":"protein_coding","ncbi_id":"728464","summary":null,"start":110245928,"end":110358272,"strand":-1,"description":"methyltransferase like 24 [Source:HGNC Symbol;Acc:HGNC:21566]"}, {"versioned_ensembl_gene_id":"ENSG00000133114.17","gene_symbol":"GPALPP1","gene_name":"GPALPP motifs containing 1 [Source:HGNC Symbol;Acc:HGNC:20298]","synonyms":"LSR7,KIAA1704,bA245H20.2,AD029","biotype":"protein_coding","ncbi_id":"55425","summary":null,"start":44989529,"end":45037669,"strand":1,"description":"GPALPP motifs containing 1 [Source:HGNC Symbol;Acc:HGNC:20298]"}, {"versioned_ensembl_gene_id":"ENSG00000250424.4","gene_symbol":"AC004691.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30852273,"end":30923812,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234370.10","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFB2,P52,TFIIH","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30986738,"end":30992660,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000272078.1","gene_symbol":"AL139423.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10639241,"end":10654333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263772.1","gene_symbol":"AC017100.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31726043,"end":31726397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233931.7","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30126512,"end":30139132,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000115592.11","gene_symbol":"PRKAG3","gene_name":"protein kinase AMP-activated non-catalytic subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:9387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53632","summary":"The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit is one of the gamma regulatory subunits of AMPK. It is dominantly expressed in skeletal muscle. Studies of the pig counterpart suggest that this subunit may play a key role in the regulation of energy metabolism in skeletal muscle. [provided by RefSeq, Jul 2008]","start":218822383,"end":218832086,"strand":-1,"description":"protein kinase AMP-activated non-catalytic subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:9387]"}, {"versioned_ensembl_gene_id":"ENSG00000257563.1","gene_symbol":"AC126755.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18402146,"end":18403604,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249309.1","gene_symbol":"AC020703.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153720327,"end":153727722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257527.1","gene_symbol":"AC126755.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18411309,"end":18411851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273289.1","gene_symbol":"AL121672.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46053093,"end":46053560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231010.1","gene_symbol":"AL121672.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46055740,"end":46058160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145428.14","gene_symbol":"RNF175","gene_name":"ring finger protein 175 [Source:HGNC Symbol;Acc:HGNC:27735]","synonyms":"FLJ34190","biotype":"protein_coding","ncbi_id":"285533","summary":null,"start":153710125,"end":153760235,"strand":-1,"description":"ring finger protein 175 [Source:HGNC Symbol;Acc:HGNC:27735]"}, {"versioned_ensembl_gene_id":"ENSG00000182257.6","gene_symbol":"PRR34","gene_name":"proline rich 34 [Source:HGNC Symbol;Acc:HGNC:25606]","synonyms":"FLJ10945,C22orf26","biotype":"protein_coding","ncbi_id":"55267","summary":null,"start":46049478,"end":46054144,"strand":-1,"description":"proline rich 34 [Source:HGNC Symbol;Acc:HGNC:25606]"}, {"versioned_ensembl_gene_id":"ENSG00000274331.1","gene_symbol":"AL355974.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109984858,"end":109986565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259316.10","gene_symbol":"AC087632.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":64181180,"end":64381510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101417.11","gene_symbol":"PXMP4","gene_name":"peroxisomal membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:15920]","synonyms":"PMP24","biotype":"protein_coding","ncbi_id":"11264","summary":null,"start":33702754,"end":33720319,"strand":-1,"description":"peroxisomal membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:15920]"}, {"versioned_ensembl_gene_id":"ENSG00000017797.12","gene_symbol":"RALBP1","gene_name":"ralA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9841]","synonyms":"RLIP76,RIP1,RIP","biotype":"protein_coding","ncbi_id":"10928","summary":"RALBP1 plays a role in receptor-mediated endocytosis and is a downstream effector of the small GTP-binding protein RAL (see RALA; MIM 179550). Small G proteins, such as RAL, have GDP-bound inactive and GTP-bound active forms, which shift from the inactive to the active state through the action of RALGDS (MIM 601619), which in turn is activated by RAS (see HRAS; MIM 190020) (summary by Feig, 2003 [PubMed 12888294]).[supplied by OMIM, Nov 2010]","start":9475009,"end":9538116,"strand":1,"description":"ralA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9841]"}, {"versioned_ensembl_gene_id":"ENSG00000116652.6","gene_symbol":"DLEU2L","gene_name":"deleted in lymphocytic leukemia 2-like [Source:HGNC Symbol;Acc:HGNC:13225]","synonyms":"BCMSUNL","biotype":"sense_intronic","ncbi_id":"79469","summary":null,"start":63547082,"end":63550636,"strand":1,"description":"deleted in lymphocytic leukemia 2-like [Source:HGNC Symbol;Acc:HGNC:13225]"}, {"versioned_ensembl_gene_id":"ENSG00000183354.11","gene_symbol":"KIAA2026","gene_name":"KIAA2026 [Source:HGNC Symbol;Acc:HGNC:23378]","synonyms":"FLJ20375","biotype":"protein_coding","ncbi_id":"158358","summary":null,"start":5881596,"end":6007901,"strand":-1,"description":"KIAA2026 [Source:HGNC Symbol;Acc:HGNC:23378]"}, {"versioned_ensembl_gene_id":"ENSG00000259985.1","gene_symbol":"AC017100.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31685655,"end":31686823,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234420.7","gene_symbol":"ZNF37BP","gene_name":"zinc finger protein 37B, pseudogene [Source:HGNC Symbol;Acc:HGNC:13103]","synonyms":"ZNF37B,KOX21,FLJ23327","biotype":"transcribed_processed_pseudogene","ncbi_id":"100129482","summary":null,"start":42513510,"end":42552822,"strand":-1,"description":"zinc finger protein 37B, pseudogene [Source:HGNC Symbol;Acc:HGNC:13103]"}, {"versioned_ensembl_gene_id":"ENSG00000229326.3","gene_symbol":"AC069154.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119698623,"end":119700151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276269.1","gene_symbol":"AL355974.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110031101,"end":110031567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239570.1","gene_symbol":"SETP11","gene_name":"SET pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419187","summary":null,"start":151269440,"end":151270129,"strand":1,"description":"SET pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42930]"}, {"versioned_ensembl_gene_id":"ENSG00000152580.8","gene_symbol":"IGSF10","gene_name":"immunoglobulin superfamily member 10 [Source:HGNC Symbol;Acc:HGNC:26384]","synonyms":"FLJ25972,CMF608","biotype":"protein_coding","ncbi_id":"285313","summary":null,"start":151425384,"end":151458709,"strand":-1,"description":"immunoglobulin superfamily member 10 [Source:HGNC Symbol;Acc:HGNC:26384]"}, {"versioned_ensembl_gene_id":"ENSG00000275830.1","gene_symbol":"AL355974.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109988097,"end":110057331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136002.18","gene_symbol":"ARHGEF4","gene_name":"Rho guanine nucleotide exchange factor 4 [Source:HGNC Symbol;Acc:HGNC:684]","synonyms":"STM6,KIAA1112,ASEF","biotype":"protein_coding","ncbi_id":"50649","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The protein encoded by this gene may form complex with G proteins and stimulate Rho-dependent signals. Multiple alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Jun 2013]","start":130836916,"end":131047263,"strand":1,"description":"Rho guanine nucleotide exchange factor 4 [Source:HGNC Symbol;Acc:HGNC:684]"}, {"versioned_ensembl_gene_id":"ENSG00000241874.1","gene_symbol":"TOMM22P6","gene_name":"TOMM22 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287573","summary":null,"start":162486541,"end":162486949,"strand":-1,"description":"TOMM22 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38742]"}, {"versioned_ensembl_gene_id":"ENSG00000260516.2","gene_symbol":"AC133548.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32356981,"end":32363695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130940.14","gene_symbol":"CASZ1","gene_name":"castor zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:26002]","synonyms":"ZNF693,SRG,FLJ20321,cst,castor","biotype":"protein_coding","ncbi_id":"54897","summary":"The protein encoded by this gene is a zinc finger transcription factor. The encoded protein may function as a tumor suppressor, and single nucleotide polymorphisms in this gene are associated with blood pressure variation. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":10636604,"end":10796650,"strand":-1,"description":"castor zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:26002]"}, {"versioned_ensembl_gene_id":"ENSG00000278167.2","gene_symbol":"CCL18","gene_name":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]","synonyms":"CKb7,SCYA18,AMAC-1,PARC,MIP-4,DCCK1,DC-CK1","biotype":"protein_coding","ncbi_id":"6362","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for naive T cells, CD4+ and CD8+ T cells and nonactivated lymphocytes, but not for monocytes or granulocytes. This chemokine attracts naive T lymphocytes toward dendritic cells and activated macrophages in lymph nodes. It may play a role in both humoral and cell-mediated immunity responses. [provided by RefSeq, Sep 2014]","start":36064636,"end":36072388,"strand":1,"description":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]"}, {"versioned_ensembl_gene_id":"ENSG00000215905.4","gene_symbol":"AL590609.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24007881,"end":24008519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243044.1","gene_symbol":"AC128716.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":162601627,"end":162601792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168438.14","gene_symbol":"CDC40","gene_name":"cell division cycle 40 [Source:HGNC Symbol;Acc:HGNC:17350]","synonyms":"PRPF17,PRP17,FLJ10564,EHB3","biotype":"protein_coding","ncbi_id":"51362","summary":"Pre-mRNA splicing occurs in two sequential transesterification steps. The protein encoded by this gene is found to be essential for the catalytic step II in pre-mRNA splicing process. It is found in the spliceosome, and contains seven WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp17 protein, which functions in two different cellular processes: pre-mRNA splicing and cell cycle progression. It suggests that this protein may play a role in cell cycle progression. [provided by RefSeq, Jul 2008]","start":110180141,"end":110254275,"strand":1,"description":"cell division cycle 40 [Source:HGNC Symbol;Acc:HGNC:17350]"}, {"versioned_ensembl_gene_id":"ENSG00000242372.6","gene_symbol":"EIF6","gene_name":"eukaryotic translation initiation factor 6 [Source:HGNC Symbol;Acc:HGNC:6159]","synonyms":"p27BBP,ITGB4BP,EIF3A,b(2)gcn","biotype":"protein_coding","ncbi_id":"3692","summary":"Hemidesmosomes are structures which link the basal lamina to the intermediate filament cytoskeleton. An important functional component of hemidesmosomes is the integrin beta-4 subunit (ITGB4), a protein containing two fibronectin type III domains. The protein encoded by this gene binds to the fibronectin type III domains of ITGB4 and may help link ITGB4 to the intermediate filament cytoskeleton. The encoded protein, which is insoluble and found both in the nucleus and in the cytoplasm, can function as a translation initiation factor and prevent the association of the 40S and 60S ribosomal subunits. Multiple non-protein coding transcript variants and variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":35278907,"end":35284985,"strand":-1,"description":"eukaryotic translation initiation factor 6 [Source:HGNC Symbol;Acc:HGNC:6159]"}, {"versioned_ensembl_gene_id":"ENSG00000231428.2","gene_symbol":"LINC00396","gene_name":"long intergenic non-protein coding RNA 396 [Source:HGNC Symbol;Acc:HGNC:42724]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355146","summary":null,"start":110053285,"end":110054952,"strand":1,"description":"long intergenic non-protein coding RNA 396 [Source:HGNC Symbol;Acc:HGNC:42724]"}, {"versioned_ensembl_gene_id":"ENSG00000181631.6","gene_symbol":"P2RY13","gene_name":"purinergic receptor P2Y13 [Source:HGNC Symbol;Acc:HGNC:4537]","synonyms":"P2Y13,GPR94,GPR86,FKSG77","biotype":"protein_coding","ncbi_id":"53829","summary":"The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is activated by ADP. [provided by RefSeq, Sep 2008]","start":151326312,"end":151329548,"strand":-1,"description":"purinergic receptor P2Y13 [Source:HGNC Symbol;Acc:HGNC:4537]"}, {"versioned_ensembl_gene_id":"ENSG00000081320.10","gene_symbol":"STK17B","gene_name":"serine/threonine kinase 17b [Source:HGNC Symbol;Acc:HGNC:11396]","synonyms":"DRAK2","biotype":"protein_coding","ncbi_id":"9262","summary":null,"start":196133566,"end":196176503,"strand":-1,"description":"serine/threonine kinase 17b [Source:HGNC Symbol;Acc:HGNC:11396]"}, {"versioned_ensembl_gene_id":"ENSG00000225315.2","gene_symbol":"AL591178.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24040835,"end":24086799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279965.1","gene_symbol":"AL390755.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":110123208,"end":110125234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235676.9","gene_symbol":"ABHD16A","gene_name":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]","synonyms":"D6S82E,BAT5,NG26","biotype":"protein_coding","ncbi_id":"7920","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":31674358,"end":31690824,"strand":-1,"description":"abhydrolase domain containing 16A [Source:HGNC Symbol;Acc:HGNC:13921]"}, {"versioned_ensembl_gene_id":"ENSG00000240583.11","gene_symbol":"AQP1","gene_name":"aquaporin 1 (Colton blood group) [Source:HGNC Symbol;Acc:HGNC:633]","synonyms":"CO,CHIP28","biotype":"protein_coding","ncbi_id":"358","summary":"This gene encodes a small integral membrane protein with six bilayer spanning domains that functions as a water channel protein. This protein permits passive transport of water along an osmotic gradient. This gene is a possible candidate for disorders involving imbalance in ocular fluid movement. [provided by RefSeq, Aug 2016]","start":30911694,"end":30925516,"strand":1,"description":"aquaporin 1 (Colton blood group) [Source:HGNC Symbol;Acc:HGNC:633]"}, {"versioned_ensembl_gene_id":"ENSG00000255830.2","gene_symbol":"AC069240.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114548854,"end":114549852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188659.9","gene_symbol":"SAXO2","gene_name":"stabilizer of axonemal microtubules 2 [Source:HGNC Symbol;Acc:HGNC:33727]","synonyms":"FAM154B,DKFZp666G057","biotype":"protein_coding","ncbi_id":"283726","summary":null,"start":82262810,"end":82284930,"strand":1,"description":"stabilizer of axonemal microtubules 2 [Source:HGNC Symbol;Acc:HGNC:33727]"}, {"versioned_ensembl_gene_id":"ENSG00000258244.1","gene_symbol":"AC069240.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114588194,"end":114588802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169313.9","gene_symbol":"P2RY12","gene_name":"purinergic receptor P2Y12 [Source:HGNC Symbol;Acc:HGNC:18124]","synonyms":"SP1999,P2Y12,HORK3","biotype":"protein_coding","ncbi_id":"64805","summary":"The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is involved in platelet aggregation, and is a potential target for the treatment of thromboembolisms and other clotting disorders. Mutations in this gene are implicated in bleeding disorder, platelet type 8 (BDPLT8). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":151337380,"end":151384812,"strand":-1,"description":"purinergic receptor P2Y12 [Source:HGNC Symbol;Acc:HGNC:18124]"}, {"versioned_ensembl_gene_id":"ENSG00000120215.9","gene_symbol":"MLANA","gene_name":"melan-A [Source:HGNC Symbol;Acc:HGNC:7124]","synonyms":"MART1","biotype":"protein_coding","ncbi_id":"2315","summary":null,"start":5890802,"end":5910606,"strand":1,"description":"melan-A [Source:HGNC Symbol;Acc:HGNC:7124]"}, {"versioned_ensembl_gene_id":"ENSG00000258254.1","gene_symbol":"AC010177.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114621761,"end":114622922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166143.9","gene_symbol":"PPP1R14D","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14D [Source:HGNC Symbol;Acc:HGNC:14953]","synonyms":"MGC119016,MGC119014,GBPI-1,FLJ20251,CPI17-like","biotype":"protein_coding","ncbi_id":"54866","summary":"Protein phosphatase-1 (PP1; see MIM 176875) is a major cellular phosphatase that reverses serine/threonine protein phosphorylation. PPP1R14D is a PP1 inhibitor that itself is regulated by phosphorylation (Liu et al., 2004 [PubMed 12974676]).[supplied by OMIM, Feb 2010]","start":40815445,"end":40828709,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14D [Source:HGNC Symbol;Acc:HGNC:14953]"}, {"versioned_ensembl_gene_id":"ENSG00000261190.5","gene_symbol":"C16orf97","gene_name":"chromosome 16 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:44658]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"388276","summary":null,"start":52005487,"end":52078474,"strand":-1,"description":"chromosome 16 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:44658]"}, {"versioned_ensembl_gene_id":"ENSG00000260151.1","gene_symbol":"AL355493.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27343436,"end":27344917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213770.3","gene_symbol":"FAM210CP","gene_name":"family with sequence similarity 210 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131328","summary":null,"start":27349717,"end":27350290,"strand":-1,"description":"family with sequence similarity 210 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44938]"}, {"versioned_ensembl_gene_id":"ENSG00000237956.1","gene_symbol":"TRIAP1P1","gene_name":"TP53 regulated inhibitor of apoptosis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31659]","synonyms":"C10orf135,bA748L13.4","biotype":"processed_pseudogene","ncbi_id":"100289619","summary":null,"start":27378138,"end":27378362,"strand":-1,"description":"TP53 regulated inhibitor of apoptosis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31659]"}, {"versioned_ensembl_gene_id":"ENSG00000266805.1","gene_symbol":"AP005432.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9506242,"end":9509726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182077.10","gene_symbol":"PTCHD3","gene_name":"patched domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24776]","synonyms":"PTR,FLJ44037","biotype":"protein_coding","ncbi_id":"374308","summary":null,"start":27398187,"end":27414368,"strand":-1,"description":"patched domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24776]"}, {"versioned_ensembl_gene_id":"ENSG00000283227.1","gene_symbol":"SPRR5","gene_name":"small proline rich protein 5 [Source:HGNC Symbol;Acc:HGNC:53428]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":152947154,"end":152949258,"strand":1,"description":"small proline rich protein 5 [Source:HGNC Symbol;Acc:HGNC:53428]"}, {"versioned_ensembl_gene_id":"ENSG00000224308.1","gene_symbol":"LINC01527","gene_name":"long intergenic non-protein coding RNA 1527 [Source:HGNC Symbol;Acc:HGNC:51266]","synonyms":"RP1-13P20.6,lnc-SPRR2D-1","biotype":"antisense_RNA","ncbi_id":"101927988","summary":null,"start":152930040,"end":152949210,"strand":-1,"description":"long intergenic non-protein coding RNA 1527 [Source:HGNC Symbol;Acc:HGNC:51266]"}, {"versioned_ensembl_gene_id":"ENSG00000139044.10","gene_symbol":"B4GALNT3","gene_name":"beta-1,4-N-acetyl-galactosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:24137]","synonyms":"FLJ40362,FLJ16224,B4GalNac-T3","biotype":"protein_coding","ncbi_id":"283358","summary":"B4GALNT3 transfers N-acetylgalactosamine (GalNAc) onto glucosyl residues to form N,N-prime-diacetyllactosediamine (LacdiNAc, or LDN), a unique terminal structure of cell surface N-glycans (Ikehara et al., 2006 [PubMed 16728562]).[supplied by OMIM, Aug 2008]","start":460364,"end":563509,"strand":1,"description":"beta-1,4-N-acetyl-galactosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:24137]"}, {"versioned_ensembl_gene_id":"ENSG00000254307.2","gene_symbol":"AP003692.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94791643,"end":94793106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216285.5","gene_symbol":"AC078819.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104030779,"end":104031543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184148.3","gene_symbol":"SPRR4","gene_name":"small proline rich protein 4 [Source:HGNC Symbol;Acc:HGNC:23173]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163778","summary":null,"start":152970666,"end":152972574,"strand":1,"description":"small proline rich protein 4 [Source:HGNC Symbol;Acc:HGNC:23173]"}, {"versioned_ensembl_gene_id":"ENSG00000120820.12","gene_symbol":"GLT8D2","gene_name":"glycosyltransferase 8 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24890]","synonyms":"FLJ31494","biotype":"protein_coding","ncbi_id":"83468","summary":null,"start":103988984,"end":104064183,"strand":-1,"description":"glycosyltransferase 8 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24890]"}, {"versioned_ensembl_gene_id":"ENSG00000229263.1","gene_symbol":"AC004691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30796691,"end":30803410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106125.14","gene_symbol":"MINDY4","gene_name":"MINDY lysine 48 deubiquitinase 4 [Source:HGNC Symbol;Acc:HGNC:21916]","synonyms":"FLJ22374,FAM188B,C7orf67","biotype":"protein_coding","ncbi_id":"84182","summary":null,"start":30771417,"end":30892387,"strand":1,"description":"MINDY lysine 48 deubiquitinase 4 [Source:HGNC Symbol;Acc:HGNC:21916]"}, {"versioned_ensembl_gene_id":"ENSG00000261470.1","gene_symbol":"AC009039.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52078622,"end":52080489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198185.11","gene_symbol":"ZNF334","gene_name":"zinc finger protein 334 [Source:HGNC Symbol;Acc:HGNC:15806]","synonyms":"bA179N14.1","biotype":"protein_coding","ncbi_id":"55713","summary":"This gene encodes a member of the C2H2 zinc finger family. The encoded protein contains a Krueppel-associated box, fourteen C2H2 zinc finger domains, and four C2H2-type/integrase DNA-binding domains. Decreased expression of this gene may be a marker for rheumatoid arthritis. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":46499630,"end":46513559,"strand":-1,"description":"zinc finger protein 334 [Source:HGNC Symbol;Acc:HGNC:15806]"}, {"versioned_ensembl_gene_id":"ENSG00000169474.4","gene_symbol":"SPRR1A","gene_name":"small proline rich protein 1A [Source:HGNC Symbol;Acc:HGNC:11259]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6698","summary":null,"start":152985231,"end":152985500,"strand":1,"description":"small proline rich protein 1A [Source:HGNC Symbol;Acc:HGNC:11259]"}, {"versioned_ensembl_gene_id":"ENSG00000279779.1","gene_symbol":"AC009039.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52081568,"end":52082096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253974.5","gene_symbol":"NRG1-IT1","gene_name":"NRG1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43633]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100856811","summary":null,"start":32026219,"end":32139475,"strand":1,"description":"NRG1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43633]"}, {"versioned_ensembl_gene_id":"ENSG00000259499.1","gene_symbol":"AC090519.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44387320,"end":44390451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116521.10","gene_symbol":"SCAMP3","gene_name":"secretory carrier membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:10565]","synonyms":"C1orf3","biotype":"protein_coding","ncbi_id":"10067","summary":"This gene encodes an integral membrane protein that belongs to the secretory carrier membrane protein family. The encoded protein functions as a carrier to the cell surface in post-golgi recycling pathways. This protein is also involved in protein trafficking in endosomal pathways. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":155255979,"end":155262430,"strand":-1,"description":"secretory carrier membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:10565]"}, {"versioned_ensembl_gene_id":"ENSG00000253505.1","gene_symbol":"AC103957.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8414690,"end":8424632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107077.18","gene_symbol":"KDM4C","gene_name":"lysine demethylase 4C [Source:HGNC Symbol;Acc:HGNC:17071]","synonyms":"TDRD14C,KIAA0780,JMJD2C,GASC1","biotype":"protein_coding","ncbi_id":"23081","summary":"This gene is a member of the Jumonji domain 2 (JMJD2) family. The encoded protein is a trimethylation-specific demethylase, and converts specific trimethylated histone residues to the dimethylated form. This enzymatic action regulates gene expression and chromosome segregation. Chromosomal aberrations and changes in expression of this gene may be found in tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":6720863,"end":7175648,"strand":1,"description":"lysine demethylase 4C [Source:HGNC Symbol;Acc:HGNC:17071]"}, {"versioned_ensembl_gene_id":"ENSG00000143398.19","gene_symbol":"PIP5K1A","gene_name":"phosphatidylinositol-4-phosphate 5-kinase type 1 alpha [Source:HGNC Symbol;Acc:HGNC:8994]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8394","summary":null,"start":151197949,"end":151249536,"strand":1,"description":"phosphatidylinositol-4-phosphate 5-kinase type 1 alpha [Source:HGNC Symbol;Acc:HGNC:8994]"}, {"versioned_ensembl_gene_id":"ENSG00000250090.1","gene_symbol":"AL390198.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25835985,"end":25836832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275048.1","gene_symbol":"BSNDP1","gene_name":"barttin CLCNK type accessory beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51536]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480329","summary":null,"start":25783553,"end":25783919,"strand":1,"description":"barttin CLCNK type accessory beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51536]"}, {"versioned_ensembl_gene_id":"ENSG00000230581.2","gene_symbol":"ACTG1P14","gene_name":"actin gamma 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49751]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418910","summary":null,"start":6834456,"end":6835577,"strand":1,"description":"actin gamma 1 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:49751]"}, {"versioned_ensembl_gene_id":"ENSG00000234433.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"NG37,G7c,C6orf27","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31756347,"end":31768050,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000267237.4","gene_symbol":"AC073135.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":198224587,"end":198224769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184032.2","gene_symbol":"KRTAP20-2","gene_name":"keratin associated protein 20-2 [Source:HGNC Symbol;Acc:HGNC:18944]","synonyms":"KAP20.2","biotype":"protein_coding","ncbi_id":"337976","summary":null,"start":30635236,"end":30635619,"strand":1,"description":"keratin associated protein 20-2 [Source:HGNC Symbol;Acc:HGNC:18944]"}, {"versioned_ensembl_gene_id":"ENSG00000284697.1","gene_symbol":"AC006511.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":8082269,"end":8138548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223957.6","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31897282,"end":31902529,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000263443.1","gene_symbol":"AC100872.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122700269,"end":122703423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253819.1","gene_symbol":"LINC01151","gene_name":"long intergenic non-protein coding RNA 1151 [Source:HGNC Symbol;Acc:HGNC:49471]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266958","summary":null,"start":122670385,"end":122694106,"strand":-1,"description":"long intergenic non-protein coding RNA 1151 [Source:HGNC Symbol;Acc:HGNC:49471]"}, {"versioned_ensembl_gene_id":"ENSG00000170745.11","gene_symbol":"KCNS3","gene_name":"potassium voltage-gated channel modifier subfamily S member 3 [Source:HGNC Symbol;Acc:HGNC:6302]","synonyms":"Kv9.3","biotype":"protein_coding","ncbi_id":"3790","summary":"Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the potassium channel family. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013]","start":17877847,"end":18361616,"strand":1,"description":"potassium voltage-gated channel modifier subfamily S member 3 [Source:HGNC Symbol;Acc:HGNC:6302]"}, {"versioned_ensembl_gene_id":"ENSG00000273225.4","gene_symbol":"FAM25BP","gene_name":"family with sequence similarity 25 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:23584]","synonyms":"FAM25B,bA144G6.8","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132929","summary":null,"start":46369113,"end":46373563,"strand":1,"description":"family with sequence similarity 25 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:23584]"}, {"versioned_ensembl_gene_id":"ENSG00000282259.1","gene_symbol":"AC216089.2","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":101334084,"end":101339373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185551.14","gene_symbol":"NR2F2","gene_name":"nuclear receptor subfamily 2 group F member 2 [Source:HGNC Symbol;Acc:HGNC:7976]","synonyms":"TFCOUP2,SVP40,NF-E3,COUPTFB,COUP-TFII,ARP1","biotype":"protein_coding","ncbi_id":"7026","summary":"This gene encodes a member of the steroid thyroid hormone superfamily of nuclear receptors. The encoded protein is a ligand inducible transcription factor that is involved in the regulation of many different genes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":96325938,"end":96340263,"strand":1,"description":"nuclear receptor subfamily 2 group F member 2 [Source:HGNC Symbol;Acc:HGNC:7976]"}, {"versioned_ensembl_gene_id":"ENSG00000124942.13","gene_symbol":"AHNAK","gene_name":"AHNAK nucleoprotein [Source:HGNC Symbol;Acc:HGNC:347]","synonyms":"MGC5395","biotype":"protein_coding","ncbi_id":"79026","summary":"The protein encoded by this gene is a large (700 kDa) structural scaffold protein consisting of a central domain with 128 aa repeats. The encoded protein may play a role in such diverse processes as blood-brain barrier formation, cell structure and migration, cardiac calcium channel regulation, and tumor metastasis. A much shorter variant encoding a 17 kDa isoform exists for this gene, and the shorter isoform initiates a feedback loop that regulates alternative splicing of this gene. [provided by RefSeq, Oct 2016]","start":62433542,"end":62556235,"strand":-1,"description":"AHNAK nucleoprotein [Source:HGNC Symbol;Acc:HGNC:347]"}, {"versioned_ensembl_gene_id":"ENSG00000174010.9","gene_symbol":"KLHL15","gene_name":"kelch like family member 15 [Source:HGNC Symbol;Acc:HGNC:29347]","synonyms":"KIAA1677","biotype":"protein_coding","ncbi_id":"80311","summary":"This gene encodes a member of the kelch-like family of proteins that share a common domain structure consisting of an N-terminal broad-complex, tramtrack, bric-a-brac/poxvirus and zinc finger domain and C-terminal kelch repeat motifs. The encoded protein may be involved in protein ubiquitination and cytoskeletal organization. [provided by RefSeq, Apr 2009]","start":23983720,"end":24027186,"strand":-1,"description":"kelch like family member 15 [Source:HGNC Symbol;Acc:HGNC:29347]"}, {"versioned_ensembl_gene_id":"ENSG00000240458.1","gene_symbol":"AC072046.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166721458,"end":166721610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187189.10","gene_symbol":"TSPYL4","gene_name":"TSPY like 4 [Source:HGNC Symbol;Acc:HGNC:21559]","synonyms":"KIAA0721,dJ486I3.2","biotype":"protein_coding","ncbi_id":"23270","summary":null,"start":116249961,"end":116254140,"strand":-1,"description":"TSPY like 4 [Source:HGNC Symbol;Acc:HGNC:21559]"}, {"versioned_ensembl_gene_id":"ENSG00000067992.12","gene_symbol":"PDK3","gene_name":"pyruvate dehydrogenase kinase 3 [Source:HGNC Symbol;Acc:HGNC:8811]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5165","summary":"The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). It provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle, and thus is one of the major enzymes responsible for the regulation of glucose metabolism. The enzymatic activity of PDH is regulated by a phosphorylation/dephosphorylation cycle, and phosphorylation results in inactivation of PDH. The protein encoded by this gene is one of the three pyruvate dehydrogenase kinases that inhibits the PDH complex by phosphorylation of the E1 alpha subunit. This gene is predominantly expressed in the heart and skeletal muscles. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":24465221,"end":24539837,"strand":1,"description":"pyruvate dehydrogenase kinase 3 [Source:HGNC Symbol;Acc:HGNC:8811]"}, {"versioned_ensembl_gene_id":"ENSG00000272275.1","gene_symbol":"AC092687.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10767875,"end":10770058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000070047.11","gene_symbol":"PHRF1","gene_name":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]","synonyms":"PPP1R125,KIAA1542,RNF221","biotype":"protein_coding","ncbi_id":"57661","summary":null,"start":576486,"end":612222,"strand":1,"description":"PHD and ring finger domains 1 [Source:HGNC Symbol;Acc:HGNC:24351]"}, {"versioned_ensembl_gene_id":"ENSG00000255325.2","gene_symbol":"AC108136.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122485515,"end":122489815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082196.20","gene_symbol":"C1QTNF3","gene_name":"C1q and TNF related 3 [Source:HGNC Symbol;Acc:HGNC:14326]","synonyms":"CTRP3,Cors-26,Cors,Corcs,2310005P21Rik","biotype":"protein_coding","ncbi_id":"114899","summary":null,"start":34019448,"end":34043832,"strand":-1,"description":"C1q and TNF related 3 [Source:HGNC Symbol;Acc:HGNC:14326]"}, {"versioned_ensembl_gene_id":"ENSG00000127337.6","gene_symbol":"YEATS4","gene_name":"YEATS domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24859]","synonyms":"YAF9,NuBI-1,GAS41","biotype":"protein_coding","ncbi_id":"8089","summary":"The protein encoded by this gene is found in the nucleoli. It has high sequence homology to human MLLT1, and yeast and human MLLT3 proteins. Both MLLT1 and MLLT3 proteins belong to a class of transcription factors, indicating that the encoded protein might also represent a transcription factor. This protein is thought to be required for RNA transcription. This gene has been shown to be amplified in tumors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":69359703,"end":69390796,"strand":1,"description":"YEATS domain containing 4 [Source:HGNC Symbol;Acc:HGNC:24859]"}, {"versioned_ensembl_gene_id":"ENSG00000236385.1","gene_symbol":"AC026355.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177621382,"end":177628287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226892.6","gene_symbol":"C6orf10","gene_name":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]","synonyms":"TSBP","biotype":"protein_coding","ncbi_id":"10665","summary":null,"start":32268544,"end":32347428,"strand":-1,"description":"chromosome 6 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:13922]"}, {"versioned_ensembl_gene_id":"ENSG00000225574.1","gene_symbol":"DRAXINP1","gene_name":"dorsal inhibitory axon guidance protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44334]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128801","summary":null,"start":8783514,"end":8784461,"strand":-1,"description":"dorsal inhibitory axon guidance protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44334]"}, {"versioned_ensembl_gene_id":"ENSG00000233668.1","gene_symbol":"AL353662.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34223984,"end":34224628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183795.8","gene_symbol":"BPY2B","gene_name":"basic charge, Y-linked, 2B [Source:HGNC Symbol;Acc:HGNC:25449]","synonyms":"VCY2B","biotype":"protein_coding","ncbi_id":"442867","summary":"This gene is located in the nonrecombining portion of the Y chromosome, and expressed specifically in testis. The encoded protein interacts with ubiquitin protein ligase E3A and may be involved in male germ cell development and male infertility. Three nearly identical copies of this gene exist on chromosome Y; two copies are part of a palindromic region. This record represents the more centromeric copy within the palindrome. [provided by RefSeq, Jul 2008]","start":24607560,"end":24639207,"strand":1,"description":"basic charge, Y-linked, 2B [Source:HGNC Symbol;Acc:HGNC:25449]"}, {"versioned_ensembl_gene_id":"ENSG00000241933.1","gene_symbol":"AC114480.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57693205,"end":57696596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234446.2","gene_symbol":"AC068489.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":221637543,"end":221641813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230406.2","gene_symbol":"AC079834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221592441,"end":221592861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264204.2","gene_symbol":"AGAP7P","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:23465]","synonyms":"CTGLF4,bA109G10.1,AGAP7","biotype":"unprocessed_pseudogene","ncbi_id":"653268","summary":null,"start":46109621,"end":46131358,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:23465]"}, {"versioned_ensembl_gene_id":"ENSG00000251266.1","gene_symbol":"LINC02429","gene_name":"long intergenic non-protein coding RNA 2429 [Source:HGNC Symbol;Acc:HGNC:53360]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377247","summary":null,"start":58984282,"end":59046959,"strand":1,"description":"long intergenic non-protein coding RNA 2429 [Source:HGNC Symbol;Acc:HGNC:53360]"}, {"versioned_ensembl_gene_id":"ENSG00000224667.1","gene_symbol":"AC013470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12506007,"end":12507478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099977.13","gene_symbol":"DDT","gene_name":"D-dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2732]","synonyms":"DDCT","biotype":"protein_coding","ncbi_id":"1652","summary":"D-dopachrome tautomerase converts D-dopachrome into 5,6-dihydroxyindole. The DDT gene is related to the migration inhibitory factor (MIF) in terms of sequence, enzyme activity, and gene structure. DDT and MIF are closely linked on chromosome 22. [provided by RefSeq, Jul 2008]","start":23971365,"end":23980469,"strand":-1,"description":"D-dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2732]"}, {"versioned_ensembl_gene_id":"ENSG00000258364.1","gene_symbol":"CR383656.13","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18636043,"end":18637421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226557.1","gene_symbol":"TRAF6P1","gene_name":"TNF receptor associated factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644871","summary":null,"start":59136625,"end":59138182,"strand":-1,"description":"TNF receptor associated factor 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45032]"}, {"versioned_ensembl_gene_id":"ENSG00000226835.2","gene_symbol":"AC097059.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94247866,"end":94334848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255814.1","gene_symbol":"LINC02439","gene_name":"long intergenic non-protein coding RNA 2439 [Source:HGNC Symbol;Acc:HGNC:53371]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370016","summary":null,"start":118818804,"end":118833536,"strand":-1,"description":"long intergenic non-protein coding RNA 2439 [Source:HGNC Symbol;Acc:HGNC:53371]"}, {"versioned_ensembl_gene_id":"ENSG00000255618.1","gene_symbol":"LINC02440","gene_name":"long intergenic non-protein coding RNA 2440 [Source:HGNC Symbol;Acc:HGNC:53372]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370015","summary":null,"start":118773032,"end":118775137,"strand":-1,"description":"long intergenic non-protein coding RNA 2440 [Source:HGNC Symbol;Acc:HGNC:53372]"}, {"versioned_ensembl_gene_id":"ENSG00000262228.2","gene_symbol":"AC087392.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":763565,"end":765319,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197683.4","gene_symbol":"KRTAP26-1","gene_name":"keratin associated protein 26-1 [Source:HGNC Symbol;Acc:HGNC:33760]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388818","summary":null,"start":30319124,"end":30320316,"strand":-1,"description":"keratin associated protein 26-1 [Source:HGNC Symbol;Acc:HGNC:33760]"}, {"versioned_ensembl_gene_id":"ENSG00000104381.12","gene_symbol":"GDAP1","gene_name":"ganglioside induced differentiation associated protein 1 [Source:HGNC Symbol;Acc:HGNC:15968]","synonyms":"CMT4A,CMT4,CMT2K","biotype":"protein_coding","ncbi_id":"54332","summary":"This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene. [provided by RefSeq, Feb 2012]","start":74321130,"end":74488872,"strand":1,"description":"ganglioside induced differentiation associated protein 1 [Source:HGNC Symbol;Acc:HGNC:15968]"}, {"versioned_ensembl_gene_id":"ENSG00000224962.4","gene_symbol":"PSAT1P4","gene_name":"phosphoserine aminotransferase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43990]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287630","summary":null,"start":166691187,"end":166691712,"strand":1,"description":"phosphoserine aminotransferase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43990]"}, {"versioned_ensembl_gene_id":"ENSG00000242498.7","gene_symbol":"ARPIN","gene_name":"actin related protein 2/3 complex inhibitor [Source:HGNC Symbol;Acc:HGNC:28782]","synonyms":"MGC61550,C15orf38","biotype":"protein_coding","ncbi_id":"348110","summary":null,"start":89895006,"end":89912956,"strand":-1,"description":"actin related protein 2/3 complex inhibitor [Source:HGNC Symbol;Acc:HGNC:28782]"}, {"versioned_ensembl_gene_id":"ENSG00000248918.2","gene_symbol":"AC008808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50969660,"end":50970187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275276.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769704,"end":54783960,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000272840.1","gene_symbol":"AC092902.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125774714,"end":125797953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279931.1","gene_symbol":"AC073593.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124725524,"end":124725934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241278.1","gene_symbol":"ENPP7P4","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48687]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421816","summary":null,"start":125848223,"end":125909372,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48687]"}, {"versioned_ensembl_gene_id":"ENSG00000261278.1","gene_symbol":"AC009094.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60024578,"end":60025141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236417.2","gene_symbol":"CTSLP1","gene_name":"cathepsin L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2539]","synonyms":"CTSLL1,CTSLL,CTSL1P1","biotype":"unprocessed_pseudogene","ncbi_id":"118945","summary":null,"start":87386685,"end":87390203,"strand":-1,"description":"cathepsin L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2539]"}, {"versioned_ensembl_gene_id":"ENSG00000279087.1","gene_symbol":"AC073592.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124637999,"end":124638444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258233.1","gene_symbol":"ARHGAP42P5","gene_name":"Rho GTPase activating protein 42 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128514","summary":null,"start":18623852,"end":18626787,"strand":-1,"description":"Rho GTPase activating protein 42 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43942]"}, {"versioned_ensembl_gene_id":"ENSG00000261466.2","gene_symbol":"AC136944.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33548297,"end":33554408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280097.1","gene_symbol":"AC073592.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124593181,"end":124593691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226738.1","gene_symbol":"U62317.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50546415,"end":50547652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254635.5","gene_symbol":"WAC-AS1","gene_name":"WAC antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27347]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"220906","summary":null,"start":28522652,"end":28532743,"strand":-1,"description":"WAC antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27347]"}, {"versioned_ensembl_gene_id":"ENSG00000239754.9","gene_symbol":"CFB","gene_name":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]","synonyms":"BFD,BF,H2-Bf","biotype":"protein_coding","ncbi_id":"629","summary":"This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]","start":31933196,"end":31939630,"strand":1,"description":"complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]"}, {"versioned_ensembl_gene_id":"ENSG00000280376.1","gene_symbol":"AC012186.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46673443,"end":46673927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274279.1","gene_symbol":"SPATA31E3P","gene_name":"SPATA31 subfamily E member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:43828]","synonyms":"FAM75E3P","biotype":"unprocessed_pseudogene","ncbi_id":"646507","summary":null,"start":22401208,"end":22406944,"strand":1,"description":"SPATA31 subfamily E member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:43828]"}, {"versioned_ensembl_gene_id":"ENSG00000228426.1","gene_symbol":"AL645634.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43665668,"end":43667005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280108.2","gene_symbol":"AJ239318.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13305152,"end":13314944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227292.1","gene_symbol":"AC009229.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38203363,"end":38239590,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176076.7","gene_symbol":"KCNE5","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 5 [Source:HGNC Symbol;Acc:HGNC:6241]","synonyms":"KCNE1L","biotype":"protein_coding","ncbi_id":"23630","summary":"This gene encodes a member of a family of single pass transmembrane domain proteins that function as ancillary subunits to voltage-gated potassium channels. Members of this family affect diverse processes in potassium channel regulation, including ion selectivity, voltage dependence, and anterograde recycling from the plasma membrane. Variants of this gene are associated with idiopathic ventricular fibrillation and Brugada syndrome. [provided by RefSeq, Nov 2016]","start":109623700,"end":109625172,"strand":-1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 5 [Source:HGNC Symbol;Acc:HGNC:6241]"}, {"versioned_ensembl_gene_id":"ENSG00000028137.18","gene_symbol":"TNFRSF1B","gene_name":"TNF receptor superfamily member 1B [Source:HGNC Symbol;Acc:HGNC:11917]","synonyms":"TNFR80,TNFR2,TNFBR,TNF-R75,TNF-R-II,p75,CD120b","biotype":"protein_coding","ncbi_id":"7133","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein and TNF-receptor 1 form a heterocomplex that mediates the recruitment of two anti-apoptotic proteins, c-IAP1 and c-IAP2, which possess E3 ubiquitin ligase activity. The function of IAPs in TNF-receptor signalling is unknown, however, c-IAP1 is thought to potentiate TNF-induced apoptosis by the ubiquitination and degradation of TNF-receptor-associated factor 2, which mediates anti-apoptotic signals. Knockout studies in mice also suggest a role of this protein in protecting neurons from apoptosis by stimulating antioxidative pathways. [provided by RefSeq, Jul 2008]","start":12167003,"end":12209228,"strand":1,"description":"TNF receptor superfamily member 1B [Source:HGNC Symbol;Acc:HGNC:11917]"}, {"versioned_ensembl_gene_id":"ENSG00000101425.12","gene_symbol":"BPI","gene_name":"bactericidal/permeability-increasing protein [Source:HGNC Symbol;Acc:HGNC:1095]","synonyms":"BPIFD1","biotype":"protein_coding","ncbi_id":"671","summary":"This gene encodes a lipopolysaccharide binding protein. It is associated with human neutrophil granules and has antimicrobial activity against gram-negative organisms. [provided by RefSeq, Nov 2014]","start":38260149,"end":38337505,"strand":1,"description":"bactericidal/permeability-increasing protein [Source:HGNC Symbol;Acc:HGNC:1095]"}, {"versioned_ensembl_gene_id":"ENSG00000279284.1","gene_symbol":"AL136967.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41381392,"end":41381832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177294.6","gene_symbol":"FBXO39","gene_name":"F-box protein 39 [Source:HGNC Symbol;Acc:HGNC:28565]","synonyms":"CT144,MGC35179,Fbx39","biotype":"protein_coding","ncbi_id":"162517","summary":"Members of the F-box protein family, such as FBXO39, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":6776223,"end":6797101,"strand":1,"description":"F-box protein 39 [Source:HGNC Symbol;Acc:HGNC:28565]"}, {"versioned_ensembl_gene_id":"ENSG00000263765.5","gene_symbol":"AC090371.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32833454,"end":32938316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262218.1","gene_symbol":"KRTAP29-1","gene_name":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]","synonyms":"KAP29.2","biotype":"protein_coding","ncbi_id":"100533177","summary":null,"start":41291504,"end":41292529,"strand":-1,"description":"keratin associated protein 29-1 [Source:HGNC Symbol;Acc:HGNC:34211]"}, {"versioned_ensembl_gene_id":"ENSG00000272945.1","gene_symbol":"AL356299.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34281632,"end":34286466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250917.1","gene_symbol":"AL035458.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":34234840,"end":34281173,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262520.1","gene_symbol":"KRTAP4-16","gene_name":"keratin associated protein 4-16 [Source:HGNC Symbol;Acc:HGNC:18921]","synonyms":"KRTAP4P1,KRTAP4-16P,KAP4A","biotype":"protein_coding","ncbi_id":"85354","summary":null,"start":41101921,"end":41102628,"strand":-1,"description":"keratin associated protein 4-16 [Source:HGNC Symbol;Acc:HGNC:18921]"}, {"versioned_ensembl_gene_id":"ENSG00000154065.16","gene_symbol":"ANKRD29","gene_name":"ankyrin repeat domain 29 [Source:HGNC Symbol;Acc:HGNC:27110]","synonyms":"FLJ25053","biotype":"protein_coding","ncbi_id":"147463","summary":null,"start":23598926,"end":23662885,"strand":-1,"description":"ankyrin repeat domain 29 [Source:HGNC Symbol;Acc:HGNC:27110]"}, {"versioned_ensembl_gene_id":"ENSG00000274457.1","gene_symbol":"AC000041.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29437583,"end":29437733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277422.1","gene_symbol":"REXO1L6P","gene_name":"REXO1 like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32243]","synonyms":"REXO1L7P","biotype":"transcribed_processed_pseudogene","ncbi_id":"441362","summary":null,"start":85826865,"end":85828467,"strand":-1,"description":"REXO1 like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32243]"}, {"versioned_ensembl_gene_id":"ENSG00000253604.1","gene_symbol":"AC131254.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29905735,"end":29908956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135916.15","gene_symbol":"ITM2C","gene_name":"integral membrane protein 2C [Source:HGNC Symbol;Acc:HGNC:6175]","synonyms":"ITM3,hRPC.1050_D_4,E25,BRICD2C,BRI3","biotype":"protein_coding","ncbi_id":"81618","summary":null,"start":230864639,"end":230879248,"strand":1,"description":"integral membrane protein 2C [Source:HGNC Symbol;Acc:HGNC:6175]"}, {"versioned_ensembl_gene_id":"ENSG00000262376.1","gene_symbol":"KRTAP2-5P","gene_name":"keratin associated protein 2-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18920]","synonyms":"KRTAP2P1,KAP2A","biotype":"unprocessed_pseudogene","ncbi_id":"85343","summary":null,"start":41072178,"end":41072573,"strand":1,"description":"keratin associated protein 2-5, pseudogene [Source:HGNC Symbol;Acc:HGNC:18920]"}, {"versioned_ensembl_gene_id":"ENSG00000232690.1","gene_symbol":"HSPE1P9","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49328]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480255","summary":null,"start":234455157,"end":234455783,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49328]"}, {"versioned_ensembl_gene_id":"ENSG00000215912.12","gene_symbol":"TTC34","gene_name":"tetratricopeptide repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:34297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287898","summary":null,"start":2635976,"end":2801717,"strand":-1,"description":"tetratricopeptide repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:34297]"}, {"versioned_ensembl_gene_id":"ENSG00000237803.5","gene_symbol":"LINC00211","gene_name":"long intergenic non-protein coding RNA 211 [Source:HGNC Symbol;Acc:HGNC:37459]","synonyms":"NCRNA00211","biotype":"lincRNA","ncbi_id":"101929559","summary":null,"start":37826247,"end":37876274,"strand":-1,"description":"long intergenic non-protein coding RNA 211 [Source:HGNC Symbol;Acc:HGNC:37459]"}, {"versioned_ensembl_gene_id":"ENSG00000156239.11","gene_symbol":"N6AMT1","gene_name":"N-6 adenine-specific DNA methyltransferase 1 (putative) [Source:HGNC Symbol;Acc:HGNC:16021]","synonyms":"PRED28,N6AMT,MTQ2,HEMK2,C21orf127","biotype":"protein_coding","ncbi_id":"29104","summary":"This gene encodes an N(6)-adenine-specific DNA methyltransferase. The encoded enzyme may be involved in the methylation of release factor I during translation termination. This enzyme is also involved in converting the arsenic metabolite monomethylarsonous acid to the less toxic dimethylarsonic acid. Alternative splicing pf this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Jul 2014]","start":28872191,"end":28885371,"strand":-1,"description":"N-6 adenine-specific DNA methyltransferase 1 (putative) [Source:HGNC Symbol;Acc:HGNC:16021]"}, {"versioned_ensembl_gene_id":"ENSG00000225942.1","gene_symbol":"LINC01875","gene_name":"long intergenic non-protein coding RNA 1875 [Source:HGNC Symbol;Acc:HGNC:52694]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927362","summary":null,"start":545805,"end":546667,"strand":1,"description":"long intergenic non-protein coding RNA 1875 [Source:HGNC Symbol;Acc:HGNC:52694]"}, {"versioned_ensembl_gene_id":"ENSG00000260030.1","gene_symbol":"AC076968.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53754358,"end":53762104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262862.2","gene_symbol":"KRTAP2-3","gene_name":"keratin associated protein 2-3 [Source:HGNC Symbol;Acc:HGNC:18906]","synonyms":"KAP2.3","biotype":"protein_coding","ncbi_id":"730755","summary":null,"start":41059470,"end":41060344,"strand":-1,"description":"keratin associated protein 2-3 [Source:HGNC Symbol;Acc:HGNC:18906]"}, {"versioned_ensembl_gene_id":"ENSG00000228981.3","gene_symbol":"AC097658.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143349275,"end":143350117,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231956.1","gene_symbol":"HNRNPA1P9","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39127]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421389","summary":null,"start":87521461,"end":87522410,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39127]"}, {"versioned_ensembl_gene_id":"ENSG00000189089.5","gene_symbol":"RIMKLBP1","gene_name":"ribosomal modification protein rimK like family member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34034]","synonyms":"FAM80C,FAM80B2,RIMKLP,RIMKLB2","biotype":"processed_pseudogene","ncbi_id":"54031","summary":null,"start":36050214,"end":36051377,"strand":1,"description":"ribosomal modification protein rimK like family member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34034]"}, {"versioned_ensembl_gene_id":"ENSG00000236119.1","gene_symbol":"AP000688.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36082859,"end":36090414,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233393.1","gene_symbol":"AP000688.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36104881,"end":36109690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211670.2","gene_symbol":"IGLV3-9","gene_name":"immunoglobulin lambda variable 3-9 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5918]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28804","summary":null,"start":22819010,"end":22819756,"strand":1,"description":"immunoglobulin lambda variable 3-9 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5918]"}, {"versioned_ensembl_gene_id":"ENSG00000275772.1","gene_symbol":"AC244157.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22785643,"end":22787268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218809.1","gene_symbol":"AL391903.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41269875,"end":41270239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277018.2","gene_symbol":"COX8C","gene_name":"cytochrome c oxidase subunit 8C [Source:HGNC Symbol;Acc:HGNC:24382]","synonyms":"COX8-3","biotype":"protein_coding","ncbi_id":"341947","summary":null,"start":93347191,"end":93348356,"strand":1,"description":"cytochrome c oxidase subunit 8C [Source:HGNC Symbol;Acc:HGNC:24382]"}, {"versioned_ensembl_gene_id":"ENSG00000150477.14","gene_symbol":"KIAA1328","gene_name":"KIAA1328 [Source:HGNC Symbol;Acc:HGNC:29248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57536","summary":null,"start":36829106,"end":37232172,"strand":1,"description":"KIAA1328 [Source:HGNC Symbol;Acc:HGNC:29248]"}, {"versioned_ensembl_gene_id":"ENSG00000095066.11","gene_symbol":"HOOK2","gene_name":"hook microtubule tethering protein 2 [Source:HGNC Symbol;Acc:HGNC:19885]","synonyms":"HK2","biotype":"protein_coding","ncbi_id":"29911","summary":"Hook proteins are cytosolic coiled-coil proteins that contain conserved N-terminal domains, which attach to microtubules, and more divergent C-terminal domains, which mediate binding to organelles. The Drosophila Hook protein is a component of the endocytic compartment.[supplied by OMIM, Apr 2004]","start":12763003,"end":12872740,"strand":-1,"description":"hook microtubule tethering protein 2 [Source:HGNC Symbol;Acc:HGNC:19885]"}, {"versioned_ensembl_gene_id":"ENSG00000178921.13","gene_symbol":"PFAS","gene_name":"phosphoribosylformylglycinamidine synthase [Source:HGNC Symbol;Acc:HGNC:8863]","synonyms":"KIAA0361,GATD8,FGARAT,PURL","biotype":"protein_coding","ncbi_id":"5198","summary":"Purines are necessary for many cellular processes, including DNA replication, transcription, and energy metabolism. Ten enzymatic steps are required to synthesize inosine monophosphate (IMP) in the de novo pathway of purine biosynthesis. The enzyme encoded by this gene catalyzes the fourth step of IMP biosynthesis. [provided by RefSeq, Jul 2008]","start":8247618,"end":8270491,"strand":1,"description":"phosphoribosylformylglycinamidine synthase [Source:HGNC Symbol;Acc:HGNC:8863]"}, {"versioned_ensembl_gene_id":"ENSG00000171223.5","gene_symbol":"JUNB","gene_name":"JunB proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3726","summary":null,"start":12791496,"end":12793315,"strand":1,"description":"JunB proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6205]"}, {"versioned_ensembl_gene_id":"ENSG00000074416.13","gene_symbol":"MGLL","gene_name":"monoglyceride lipase [Source:HGNC Symbol;Acc:HGNC:17038]","synonyms":"MGL,HU-K5","biotype":"protein_coding","ncbi_id":"11343","summary":"This gene encodes a serine hydrolase of the AB hydrolase superfamily that catalyzes the conversion of monoacylglycerides to free fatty acids and glycerol. The encoded protein plays a critical role in several physiological processes including pain and nociperception through hydrolysis of the endocannabinoid 2-arachidonoylglycerol. Expression of this gene may play a role in cancer tumorigenesis and metastasis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]","start":127689062,"end":127823250,"strand":-1,"description":"monoglyceride lipase [Source:HGNC Symbol;Acc:HGNC:17038]"}, {"versioned_ensembl_gene_id":"ENSG00000230122.1","gene_symbol":"ECEL1P3","gene_name":"endothelin converting enzyme like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:14018]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"260332","summary":null,"start":232349754,"end":232351309,"strand":-1,"description":"endothelin converting enzyme like 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:14018]"}, {"versioned_ensembl_gene_id":"ENSG00000267524.1","gene_symbol":"RPSAP57","gene_name":"ribosomal protein SA pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:35889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390857","summary":null,"start":54744750,"end":54745581,"strand":1,"description":"ribosomal protein SA pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:35889]"}, {"versioned_ensembl_gene_id":"ENSG00000267112.1","gene_symbol":"AC098848.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54885866,"end":54898083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219329.1","gene_symbol":"AL357515.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110923566,"end":110924107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243144.6","gene_symbol":"AC079760.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91311368,"end":91515409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280202.1","gene_symbol":"AC005831.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3610307,"end":3612003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235450.1","gene_symbol":"AC079760.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91380778,"end":91556848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228167.1","gene_symbol":"AL353072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":194718795,"end":194719236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110484.6","gene_symbol":"SCGB2A2","gene_name":"secretoglobin family 2A member 2 [Source:HGNC Symbol;Acc:HGNC:7050]","synonyms":"UGB2,MGC71974,MGB1","biotype":"protein_coding","ncbi_id":"4250","summary":null,"start":62270155,"end":62273156,"strand":1,"description":"secretoglobin family 2A member 2 [Source:HGNC Symbol;Acc:HGNC:7050]"}, {"versioned_ensembl_gene_id":"ENSG00000211660.3","gene_symbol":"IGLV2-23","gene_name":"immunoglobulin lambda variable 2-23 [Source:HGNC Symbol;Acc:HGNC:5890]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28813","summary":null,"start":22697789,"end":22698407,"strand":1,"description":"immunoglobulin lambda variable 2-23 [Source:HGNC Symbol;Acc:HGNC:5890]"}, {"versioned_ensembl_gene_id":"ENSG00000185847.7","gene_symbol":"LINC01405","gene_name":"long intergenic non-protein coding RNA 1405 [Source:HGNC Symbol;Acc:HGNC:50688]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100131138","summary":null,"start":110936585,"end":110958208,"strand":1,"description":"long intergenic non-protein coding RNA 1405 [Source:HGNC Symbol;Acc:HGNC:50688]"}, {"versioned_ensembl_gene_id":"ENSG00000279814.1","gene_symbol":"AC010997.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":75450081,"end":75451725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157456.7","gene_symbol":"CCNB2","gene_name":"cyclin B2 [Source:HGNC Symbol;Acc:HGNC:1580]","synonyms":"HsT17299","biotype":"protein_coding","ncbi_id":"9133","summary":"Cyclin B2 is a member of the cyclin family, specifically the B-type cyclins. The B-type cyclins, B1 and B2, associate with p34cdc2 and are essential components of the cell cycle regulatory machinery. B1 and B2 differ in their subcellular localization. Cyclin B1 co-localizes with microtubules, whereas cyclin B2 is primarily associated with the Golgi region. Cyclin B2 also binds to transforming growth factor beta RII and thus cyclin B2/cdc2 may play a key role in transforming growth factor beta-mediated cell cycle control. [provided by RefSeq, Jul 2008]","start":59105078,"end":59125045,"strand":1,"description":"cyclin B2 [Source:HGNC Symbol;Acc:HGNC:1580]"}, {"versioned_ensembl_gene_id":"ENSG00000081985.10","gene_symbol":"IL12RB2","gene_name":"interleukin 12 receptor subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:5972]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3595","summary":"The protein encoded by this gene is a type I transmembrane protein identified as a subunit of the interleukin 12 receptor complex. The coexpression of this and IL12RB1 proteins was shown to lead to the formation of high-affinity IL12 binding sites and reconstitution of IL12 dependent signaling. The expression of this gene is up-regulated by interferon gamma in Th1 cells, and plays a role in Th1 cell differentiation. The up-regulation of this gene is found to be associated with a number of infectious diseases, such as Crohn's disease and leprosy, which is thought to contribute to the inflammatory response and host defense. Several transcript variants encoding different isoforms and non-protein coding transcripts have been found for this gene. [provided by RefSeq, Apr 2012]","start":67307364,"end":67396900,"strand":1,"description":"interleukin 12 receptor subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:5972]"}, {"versioned_ensembl_gene_id":"ENSG00000263101.2","gene_symbol":"KRTAP3-3","gene_name":"keratin associated protein 3-3 [Source:HGNC Symbol;Acc:HGNC:18890]","synonyms":"KAP3.3","biotype":"protein_coding","ncbi_id":"85293","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":40993557,"end":40994260,"strand":-1,"description":"keratin associated protein 3-3 [Source:HGNC Symbol;Acc:HGNC:18890]"}, {"versioned_ensembl_gene_id":"ENSG00000277162.1","gene_symbol":"U85056.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":190065233,"end":190065914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204618.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"LIRF,HZFw1","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30070266,"end":30075887,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000146376.10","gene_symbol":"ARHGAP18","gene_name":"Rho GTPase activating protein 18 [Source:HGNC Symbol;Acc:HGNC:21035]","synonyms":"MacGAP,bA307O14.2","biotype":"protein_coding","ncbi_id":"93663","summary":"ARHGAP18 belongs to a family of Rho (see MIM 165390) GTPase-activating proteins that modulate cell signaling (Potkin et al., 2009 [PubMed 19065146]).[supplied by OMIM, Apr 2010]","start":129576132,"end":129710225,"strand":-1,"description":"Rho GTPase activating protein 18 [Source:HGNC Symbol;Acc:HGNC:21035]"}, {"versioned_ensembl_gene_id":"ENSG00000258632.2","gene_symbol":"AC135626.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94273496,"end":94274005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257453.1","gene_symbol":"AC011611.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76030494,"end":76031378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237765.6","gene_symbol":"FAM200B","gene_name":"family with sequence similarity 200 member B [Source:HGNC Symbol;Acc:HGNC:27740]","synonyms":"C4orf53","biotype":"protein_coding","ncbi_id":"285550","summary":null,"start":15681662,"end":15705565,"strand":1,"description":"family with sequence similarity 200 member B [Source:HGNC Symbol;Acc:HGNC:27740]"}, {"versioned_ensembl_gene_id":"ENSG00000280220.1","gene_symbol":"AL157414.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57161822,"end":57163775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278692.1","gene_symbol":"GU182355.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54754729,"end":54769262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064703.11","gene_symbol":"DDX20","gene_name":"DEAD-box helicase 20 [Source:HGNC Symbol;Acc:HGNC:2743]","synonyms":"GEMIN3,DP103","biotype":"protein_coding","ncbi_id":"11218","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which has an ATPase activity and is a component of the survival of motor neurons (SMN) complex. This protein interacts directly with SMN, the spinal muscular atrophy gene product, and may play a catalytic role in the function of the SMN complex on RNPs. [provided by RefSeq, Jul 2008]","start":111755245,"end":111768016,"strand":1,"description":"DEAD-box helicase 20 [Source:HGNC Symbol;Acc:HGNC:2743]"}, {"versioned_ensembl_gene_id":"ENSG00000250326.1","gene_symbol":"AC104596.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142933195,"end":143184861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064607.16","gene_symbol":"SUGP2","gene_name":"SURP and G-patch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18641]","synonyms":"SFRS14,KIAA0365","biotype":"protein_coding","ncbi_id":"10147","summary":"This gene encodes a member of the arginine/serine-rich family of splicing factors. The encoded protein functions in mRNA processing. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":18990888,"end":19034023,"strand":-1,"description":"SURP and G-patch domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18641]"}, {"versioned_ensembl_gene_id":"ENSG00000237513.1","gene_symbol":"AC007384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":104941063,"end":104962334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261834.2","gene_symbol":"IGHV3OR16-15","gene_name":"immunoglobulin heavy variable 3/OR16-15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5639]","synonyms":"IGHV3/OR16-15","biotype":"IG_V_pseudogene","ncbi_id":"28301","summary":null,"start":32903442,"end":32903894,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5639]"}, {"versioned_ensembl_gene_id":"ENSG00000240236.1","gene_symbol":"HNRNPA1P23","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39541]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130002","summary":null,"start":122317609,"end":122318741,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39541]"}, {"versioned_ensembl_gene_id":"ENSG00000279549.1","gene_symbol":"AP000437.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61143380,"end":61145464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270764.1","gene_symbol":"AC005070.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105189190,"end":105189814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237280.1","gene_symbol":"AL136982.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87113954,"end":87115523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272918.1","gene_symbol":"AC005070.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105102838,"end":105105483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241035.2","gene_symbol":"AL161747.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21398925,"end":21399282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258870.1","gene_symbol":"EIF4EBP1P1","gene_name":"eukaryotic translation initiation factor 4E binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20160]","synonyms":"EIF4EBP1P","biotype":"processed_pseudogene","ncbi_id":"326295","summary":null,"start":21419620,"end":21419960,"strand":1,"description":"eukaryotic translation initiation factor 4E binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20160]"}, {"versioned_ensembl_gene_id":"ENSG00000235569.12","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31730217,"end":31751987,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000265519.1","gene_symbol":"AC015922.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15787787,"end":15788205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174004.5","gene_symbol":"NRROS","gene_name":"negative regulator of reactive oxygen species [Source:HGNC Symbol;Acc:HGNC:24613]","synonyms":"UNQ3030,MGC50789,LRRC33,GARPL1,ELLP3030","biotype":"protein_coding","ncbi_id":"375387","summary":null,"start":196639686,"end":196662004,"strand":1,"description":"negative regulator of reactive oxygen species [Source:HGNC Symbol;Acc:HGNC:24613]"}, {"versioned_ensembl_gene_id":"ENSG00000101882.9","gene_symbol":"NKAP","gene_name":"NFKB activating protein [Source:HGNC Symbol;Acc:HGNC:29873]","synonyms":"FLJ22626","biotype":"protein_coding","ncbi_id":"79576","summary":"This gene encodes a protein that is involved in the activation of the ubiquitous transcription factor NF-kappaB. This protein is associated with the the histone deacetylase HDAC3 and with the Notch corepressor complex, and it thereby acts as a transcriptional repressor of Notch target genes. It is also required for alphabeta T cell development. A related pseudogene has been identified on chromosome X, while a related and intronless retrocopy, which has an intact CDS and may be functional, is located on chromosome 6. [provided by RefSeq, May 2010]","start":119920672,"end":119943772,"strand":-1,"description":"NFKB activating protein [Source:HGNC Symbol;Acc:HGNC:29873]"}, {"versioned_ensembl_gene_id":"ENSG00000229822.2","gene_symbol":"AL353691.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41748222,"end":41748608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176014.12","gene_symbol":"TUBB6","gene_name":"tubulin beta 6 class V [Source:HGNC Symbol;Acc:HGNC:20776]","synonyms":"MGC4083,HsT1601","biotype":"protein_coding","ncbi_id":"84617","summary":null,"start":12307669,"end":12344320,"strand":1,"description":"tubulin beta 6 class V [Source:HGNC Symbol;Acc:HGNC:20776]"}, {"versioned_ensembl_gene_id":"ENSG00000171657.5","gene_symbol":"GPR82","gene_name":"G protein-coupled receptor 82 [Source:HGNC Symbol;Acc:HGNC:4533]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27197","summary":"The protein encoded by this gene is an orphan G protein-coupled receptor of unknown function. The encoded protein is a member of a family of proteins that contain seven transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. [provided by RefSeq, Sep 2011]","start":41724155,"end":41730135,"strand":1,"description":"G protein-coupled receptor 82 [Source:HGNC Symbol;Acc:HGNC:4533]"}, {"versioned_ensembl_gene_id":"ENSG00000270304.1","gene_symbol":"AC087283.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37253879,"end":37254952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120875.8","gene_symbol":"DUSP4","gene_name":"dual specificity phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3070]","synonyms":"TYP,MKP-2,HVH2","biotype":"protein_coding","ncbi_id":"1846","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates ERK1, ERK2 and JNK, is expressed in a variety of tissues, and is localized in the nucleus. Two alternatively spliced transcript variants, encoding distinct isoforms, have been observed for this gene. In addition, multiple polyadenylation sites have been reported. [provided by RefSeq, Jul 2008]","start":29333064,"end":29350668,"strand":-1,"description":"dual specificity phosphatase 4 [Source:HGNC Symbol;Acc:HGNC:3070]"}, {"versioned_ensembl_gene_id":"ENSG00000280114.1","gene_symbol":"AL021920.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16681097,"end":16688749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268869.5","gene_symbol":"ESPNP","gene_name":"espin pseudogene [Source:HGNC Symbol;Acc:HGNC:23285]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284729","summary":null,"start":16687339,"end":16720157,"strand":-1,"description":"espin pseudogene [Source:HGNC Symbol;Acc:HGNC:23285]"}, {"versioned_ensembl_gene_id":"ENSG00000275608.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54802886,"end":54817473,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000279151.1","gene_symbol":"AL021920.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16701546,"end":16705594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236698.1","gene_symbol":"EIF1AXP1","gene_name":"eukaryotic translation initiation factor 1A, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19900]","synonyms":"EIF1AP1","biotype":"processed_pseudogene","ncbi_id":"280661","summary":null,"start":16685621,"end":16686055,"strand":-1,"description":"eukaryotic translation initiation factor 1A, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19900]"}, {"versioned_ensembl_gene_id":"ENSG00000135324.5","gene_symbol":"MRAP2","gene_name":"melanocortin 2 receptor accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:21232]","synonyms":"C6orf117,bA51G5.2","biotype":"protein_coding","ncbi_id":"112609","summary":"This gene encodes a protein that modulates melanocortin receptor signaling. The encoded protein has been shown to interact with all known melanocortin receptors and may regulate both receptor trafficking and activation in response to ligands. Mice lacking a functional copy of this gene exhibit severe obesity and a mutation in this gene may be associated with severe obesity in human patients. [provided by RefSeq, Oct 2016]","start":84033756,"end":84090881,"strand":1,"description":"melanocortin 2 receptor accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:21232]"}, {"versioned_ensembl_gene_id":"ENSG00000265107.2","gene_symbol":"GJA5","gene_name":"gap junction protein alpha 5 [Source:HGNC Symbol;Acc:HGNC:4279]","synonyms":"CX40","biotype":"protein_coding","ncbi_id":"2702","summary":"This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene may be associated with atrial fibrillation. Alternatively spliced transcript variants encoding the same isoform have been described. [provided by RefSeq, Jul 2008]","start":147756199,"end":147773362,"strand":-1,"description":"gap junction protein alpha 5 [Source:HGNC Symbol;Acc:HGNC:4279]"}, {"versioned_ensembl_gene_id":"ENSG00000271941.1","gene_symbol":"AC104184.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43346923,"end":43347643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223916.1","gene_symbol":"AC097638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43484972,"end":43485880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166509.10","gene_symbol":"CLEC3A","gene_name":"C-type lectin domain family 3 member A [Source:HGNC Symbol;Acc:HGNC:2052]","synonyms":"CLECSF1","biotype":"protein_coding","ncbi_id":"10143","summary":null,"start":78022515,"end":78066761,"strand":1,"description":"C-type lectin domain family 3 member A [Source:HGNC Symbol;Acc:HGNC:2052]"}, {"versioned_ensembl_gene_id":"ENSG00000274415.1","gene_symbol":"AC241644.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147757185,"end":147758434,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087510.6","gene_symbol":"TFAP2C","gene_name":"transcription factor AP-2 gamma [Source:HGNC Symbol;Acc:HGNC:11744]","synonyms":"ERF1,AP2-GAMMA,TFAP2G,hAP-2g","biotype":"protein_coding","ncbi_id":"7022","summary":"The protein encoded by this gene is a sequence-specific DNA-binding transcription factor involved in the activation of several developmental genes. The encoded protein can act as either a homodimer or heterodimer with other family members and is induced during retinoic acid-mediated differentiation. It plays a role in the development of the eyes, face, body wall, limbs, and neural tube. [provided by RefSeq, Jul 2008]","start":56629302,"end":56639283,"strand":1,"description":"transcription factor AP-2 gamma [Source:HGNC Symbol;Acc:HGNC:11744]"}, {"versioned_ensembl_gene_id":"ENSG00000231236.2","gene_symbol":"AP001605.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27358885,"end":27448579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244119.1","gene_symbol":"PDCL3P4","gene_name":"phosducin-like 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44505]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285359","summary":null,"start":101712472,"end":101713191,"strand":1,"description":"phosducin-like 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44505]"}, {"versioned_ensembl_gene_id":"ENSG00000276302.1","gene_symbol":"AL021997.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28267121,"end":28281580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130702.15","gene_symbol":"LAMA5","gene_name":"laminin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3911","summary":"This gene encodes one of the vertebrate laminin alpha chains. Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. The protein encoded by this gene is the alpha-5 subunit of of laminin-10 (laminin-511), laminin-11 (laminin-521) and laminin-15 (laminin-523). [provided by RefSeq, Jun 2013]","start":62307955,"end":62367312,"strand":-1,"description":"laminin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]"}, {"versioned_ensembl_gene_id":"ENSG00000158856.18","gene_symbol":"DMTN","gene_name":"dematin actin binding protein [Source:HGNC Symbol;Acc:HGNC:3382]","synonyms":"EPB49,DMT","biotype":"protein_coding","ncbi_id":"2039","summary":"The protein encoded by this gene is an actin binding and bundling protein that plays a structural role in erythrocytes, by stabilizing and attaching the spectrin/actin cytoskeleton to the erythrocyte membrane in a phosphorylation-dependent manner. This protein contains a core domain in the N-terminus, and a headpiece domain in the C-terminus that binds F-actin. When purified from erythrocytes, this protein exists as a trimer composed of two 48 kDa polypeptides and a 52 kDa polypeptide. The different subunits arise from alternative splicing in the 3' coding region, where the headpiece domain is located. Disruption of this gene has been correlated with the autosomal dominant Marie Unna hereditary hypotrichosis disease, while loss of heterozygosity of this gene is thought to play a role in prostate cancer progression. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2014]","start":22048995,"end":22082527,"strand":1,"description":"dematin actin binding protein [Source:HGNC Symbol;Acc:HGNC:3382]"}, {"versioned_ensembl_gene_id":"ENSG00000214760.3","gene_symbol":"RPL21P1","gene_name":"ribosomal protein L21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10314]","synonyms":"RPL21P","biotype":"processed_pseudogene","ncbi_id":"6145","summary":null,"start":122364782,"end":122365632,"strand":1,"description":"ribosomal protein L21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10314]"}, {"versioned_ensembl_gene_id":"ENSG00000284610.1","gene_symbol":"AC107918.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12006188,"end":12015193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235955.1","gene_symbol":"CICP20","gene_name":"capicua transcriptional repressor pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:48830]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129050","summary":null,"start":45816216,"end":45819016,"strand":-1,"description":"capicua transcriptional repressor pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:48830]"}, {"versioned_ensembl_gene_id":"ENSG00000278248.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769801,"end":54784302,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000113638.13","gene_symbol":"TTC33","gene_name":"tetratricopeptide repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:29959]","synonyms":"OSRF","biotype":"protein_coding","ncbi_id":"23548","summary":null,"start":40512333,"end":40755975,"strand":-1,"description":"tetratricopeptide repeat domain 33 [Source:HGNC Symbol;Acc:HGNC:29959]"}, {"versioned_ensembl_gene_id":"ENSG00000269471.1","gene_symbol":"AC092329.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23204010,"end":23204556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273740.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54628233,"end":54632455,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000179886.5","gene_symbol":"TIGD5","gene_name":"tigger transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:18336]","synonyms":"FLJ14926","biotype":"protein_coding","ncbi_id":"84948","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":143597835,"end":143603224,"strand":1,"description":"tigger transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:18336]"}, {"versioned_ensembl_gene_id":"ENSG00000169607.12","gene_symbol":"CKAP2L","gene_name":"cytoskeleton associated protein 2 like [Source:HGNC Symbol;Acc:HGNC:26877]","synonyms":"radmis,FLJ40629","biotype":"protein_coding","ncbi_id":"150468","summary":"The protein encoded by this gene is thought to be a mitotic spindle protein important to neural stem or progenitor cells. Mutations in this gene have been associated with spindle organization defects, including mitotic spindle defects, lagging chromosomes, and chromatin bridges. There is evidence that mutations in this gene are associated with Filippi syndrome, characterized by growth defects, microcephaly, intellectual disability, facial feature defects, and syndactyly. There is a pseudogene of this gene on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":112736607,"end":112764677,"strand":-1,"description":"cytoskeleton associated protein 2 like [Source:HGNC Symbol;Acc:HGNC:26877]"}, {"versioned_ensembl_gene_id":"ENSG00000233129.1","gene_symbol":"AL117351.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93934479,"end":93935244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187762.5","gene_symbol":"HSPE1P11","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49330]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481673","summary":null,"start":35023522,"end":35023831,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49330]"}, {"versioned_ensembl_gene_id":"ENSG00000225657.2","gene_symbol":"LINC01716","gene_name":"long intergenic non-protein coding RNA 1716 [Source:HGNC Symbol;Acc:HGNC:52503]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372682","summary":null,"start":56577563,"end":56598621,"strand":1,"description":"long intergenic non-protein coding RNA 1716 [Source:HGNC Symbol;Acc:HGNC:52503]"}, {"versioned_ensembl_gene_id":"ENSG00000125352.5","gene_symbol":"RNF113A","gene_name":"ring finger protein 113A [Source:HGNC Symbol;Acc:HGNC:12974]","synonyms":"Cwc24,ZNF183,RNF113","biotype":"protein_coding","ncbi_id":"7737","summary":"This intronless gene encodes a protein which contains a C3H1-type zinc finger domain and a C3HC4 Ring-type (Really Interesting New Gene-type) zinc finger domain. The Ring-type zinc finger domain is identified in various tumor suppressors, DNA repair genes and cytokine receptor-associated molecules, and is probably involved in mediating protein-protein interactions. [provided by RefSeq, May 2010]","start":119870475,"end":119871827,"strand":-1,"description":"ring finger protein 113A [Source:HGNC Symbol;Acc:HGNC:12974]"}, {"versioned_ensembl_gene_id":"ENSG00000225329.3","gene_symbol":"LHFPL3-AS2","gene_name":"LHFPL3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44106]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"723809","summary":null,"start":104894628,"end":104926645,"strand":-1,"description":"LHFPL3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44106]"}, {"versioned_ensembl_gene_id":"ENSG00000276798.4","gene_symbol":"LILRA4","gene_name":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]","synonyms":"ILT7,CD85g","biotype":"protein_coding","ncbi_id":"23547","summary":"This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015]","start":54315894,"end":54346149,"strand":-1,"description":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]"}, {"versioned_ensembl_gene_id":"ENSG00000125772.12","gene_symbol":"GPCPD1","gene_name":"glycerophosphocholine phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:26957]","synonyms":"KIAA1434,GDPD6,GDE5","biotype":"protein_coding","ncbi_id":"56261","summary":null,"start":5544404,"end":5611026,"strand":-1,"description":"glycerophosphocholine phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:26957]"}, {"versioned_ensembl_gene_id":"ENSG00000232205.1","gene_symbol":"CDY18P","gene_name":"chromodomain Y-linked 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:23862]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386740","summary":null,"start":24104107,"end":24106018,"strand":1,"description":"chromodomain Y-linked 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:23862]"}, {"versioned_ensembl_gene_id":"ENSG00000229185.4","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29584054,"end":29585637,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000154734.14","gene_symbol":"ADAMTS1","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 1 [Source:HGNC Symbol;Acc:HGNC:217]","synonyms":"KIAA1346,C3-C5,METH1","biotype":"protein_coding","ncbi_id":"9510","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene contains two disintegrin loops and three C-terminal TS motifs and has anti-angiogenic activity. The expression of this gene may be associated with various inflammatory processes as well as development of cancer cachexia. This gene is likely to be necessary for normal growth, fertility, and organ morphology and function. [provided by RefSeq, Jul 2008]","start":26835747,"end":26845409,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 1 [Source:HGNC Symbol;Acc:HGNC:217]"}, {"versioned_ensembl_gene_id":"ENSG00000273013.1","gene_symbol":"AC117490.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":196474801,"end":196475394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230273.1","gene_symbol":"AC087163.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17981192,"end":17981572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228958.1","gene_symbol":"PIGPP3","gene_name":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45155]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128033","summary":null,"start":33965162,"end":33965576,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45155]"}, {"versioned_ensembl_gene_id":"ENSG00000182902.13","gene_symbol":"SLC25A18","gene_name":"solute carrier family 25 member 18 [Source:HGNC Symbol;Acc:HGNC:10988]","synonyms":null,"biotype":"protein_coding","ncbi_id":"83733","summary":null,"start":17563439,"end":17590994,"strand":1,"description":"solute carrier family 25 member 18 [Source:HGNC Symbol;Acc:HGNC:10988]"}, {"versioned_ensembl_gene_id":"ENSG00000181378.13","gene_symbol":"CFAP65","gene_name":"cilia and flagella associated protein 65 [Source:HGNC Symbol;Acc:HGNC:25325]","synonyms":"MGC35338,DKFZp434O0527,CCDC108","biotype":"protein_coding","ncbi_id":"255101","summary":"The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. The chicken ortholog of this gene is involved in the Rose-comb mutation, which is a large chromosome inversion, resulting in altered comb morphology and defects in sperm motility. [provided by RefSeq, Aug 2016]","start":219002846,"end":219041527,"strand":-1,"description":"cilia and flagella associated protein 65 [Source:HGNC Symbol;Acc:HGNC:25325]"}, {"versioned_ensembl_gene_id":"ENSG00000219404.2","gene_symbol":"AL359694.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22213306,"end":22214237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149600.11","gene_symbol":"COMMD7","gene_name":"COMM domain containing 7 [Source:HGNC Symbol;Acc:HGNC:16223]","synonyms":"dJ1085F17.3,C20orf92","biotype":"protein_coding","ncbi_id":"149951","summary":null,"start":32702691,"end":32743997,"strand":-1,"description":"COMM domain containing 7 [Source:HGNC Symbol;Acc:HGNC:16223]"}, {"versioned_ensembl_gene_id":"ENSG00000068078.17","gene_symbol":"FGFR3","gene_name":"fibroblast growth factor receptor 3 [Source:HGNC Symbol;Acc:HGNC:3690]","synonyms":"JTK4,CEK2,CD333,ACH","biotype":"protein_coding","ncbi_id":"2261","summary":"This gene encodes a member of the fibroblast growth factor receptor (FGFR) family, with its amino acid sequence being highly conserved between members and among divergent species. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds acidic and basic fibroblast growth hormone and plays a role in bone development and maintenance. Mutations in this gene lead to craniosynostosis and multiple types of skeletal dysplasia. [provided by RefSeq, Aug 2017]","start":1793307,"end":1808872,"strand":1,"description":"fibroblast growth factor receptor 3 [Source:HGNC Symbol;Acc:HGNC:3690]"}, {"versioned_ensembl_gene_id":"ENSG00000265490.1","gene_symbol":"AP001178.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":706523,"end":707648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233350.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"TRIM26P,Em:AB023053.1,TRIM26P1","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30228650,"end":30232212,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000164941.13","gene_symbol":"INTS8","gene_name":"integrator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:26048]","synonyms":"MGC131633,INT8,FLJ20530,C8orf52","biotype":"protein_coding","ncbi_id":"55656","summary":"This gene encodes a subunit of the Integrator complex which is involved in the cleavage of small nuclear RNAs U1 and U2 within the nucleus. The encoded protein associates with RNA polymerase II and is recruited to the U1 and U2 small nuclear RNA genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":94813311,"end":94881746,"strand":1,"description":"integrator complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:26048]"}, {"versioned_ensembl_gene_id":"ENSG00000257497.2","gene_symbol":"AC121761.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75483454,"end":75489820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248611.1","gene_symbol":"AC107385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154555208,"end":154555985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131808.10","gene_symbol":"FSHB","gene_name":"follicle stimulating hormone beta subunit [Source:HGNC Symbol;Acc:HGNC:3964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2488","summary":"The pituitary glycoprotein hormone family includes follicle-stimulating hormone, luteinizing hormone, chorionic gonadotropin, and thyroid-stimulating hormone. All of these glycoproteins consist of an identical alpha subunit and a hormone-specific beta subunit. This gene encodes the beta subunit of follicle-stimulating hormone. In conjunction with luteinizing hormone, follicle-stimulating hormone induces egg and sperm production. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":30231016,"end":30235261,"strand":1,"description":"follicle stimulating hormone beta subunit [Source:HGNC Symbol;Acc:HGNC:3964]"}, {"versioned_ensembl_gene_id":"ENSG00000173705.8","gene_symbol":"SUSD5","gene_name":"sushi domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29061]","synonyms":"KIAA0527","biotype":"protein_coding","ncbi_id":"26032","summary":null,"start":33150042,"end":33219215,"strand":-1,"description":"sushi domain containing 5 [Source:HGNC Symbol;Acc:HGNC:29061]"}, {"versioned_ensembl_gene_id":"ENSG00000124104.18","gene_symbol":"SNX21","gene_name":"sorting nexin family member 21 [Source:HGNC Symbol;Acc:HGNC:16154]","synonyms":"SNX-L,dJ337O18.4,C20orf161","biotype":"protein_coding","ncbi_id":"90203","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":45833810,"end":45843275,"strand":1,"description":"sorting nexin family member 21 [Source:HGNC Symbol;Acc:HGNC:16154]"}, {"versioned_ensembl_gene_id":"ENSG00000101421.3","gene_symbol":"CHMP4B","gene_name":"charged multivesicular body protein 4B [Source:HGNC Symbol;Acc:HGNC:16171]","synonyms":"C20orf178,VPS32B,SNF7-2,Shax1,dJ553F4.4","biotype":"protein_coding","ncbi_id":"128866","summary":"This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein (CHMP) protein family. The protein is part of the endosomal sorting complex required for transport (ESCRT) complex III (ESCRT-III), which functions in the sorting of endocytosed cell-surface receptors into multivesicular endosomes. The ESCRT machinery also functions in the final abscisson stage of cytokinesis and in the budding of enveloped viruses such as HIV-1. The three proteins of the CHMP4 subfamily interact with programmed cell death 6 interacting protein (PDCD6IP, also known as ALIX), which also functions in the ESCRT pathway. The CHMP4 proteins assemble into membrane-attached 5-nm filaments that form circular scaffolds and promote or stabilize outward budding. These polymers are proposed to help generate the luminal vesicles of multivesicular bodies. Mutations in this gene result in autosomal dominant posterior polar cataracts.[provided by RefSeq, Oct 2009]","start":33811304,"end":33854366,"strand":1,"description":"charged multivesicular body protein 4B [Source:HGNC Symbol;Acc:HGNC:16171]"}, {"versioned_ensembl_gene_id":"ENSG00000115275.11","gene_symbol":"MOGS","gene_name":"mannosyl-oligosaccharide glucosidase [Source:HGNC Symbol;Acc:HGNC:24862]","synonyms":"GCS1,DER7,CWH41","biotype":"protein_coding","ncbi_id":"7841","summary":"This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":74461057,"end":74465410,"strand":-1,"description":"mannosyl-oligosaccharide glucosidase [Source:HGNC Symbol;Acc:HGNC:24862]"}, {"versioned_ensembl_gene_id":"ENSG00000234008.5","gene_symbol":"PPP1R2P2","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54036","summary":null,"start":35887195,"end":35887807,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:9290]"}, {"versioned_ensembl_gene_id":"ENSG00000230794.1","gene_symbol":"AF015720.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35713139,"end":35732942,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277602.1","gene_symbol":"AC005363.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1971655,"end":1971896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282753.1","gene_symbol":"AC068594.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77275802,"end":77276398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249458.1","gene_symbol":"AC092673.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176866614,"end":176875457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282649.1","gene_symbol":"AC068594.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77269359,"end":77293519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235499.1","gene_symbol":"AC073046.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73985132,"end":73986343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268296.1","gene_symbol":"AC022145.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22907086,"end":22914289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004809.13","gene_symbol":"SLC22A16","gene_name":"solute carrier family 22 member 16 [Source:HGNC Symbol;Acc:HGNC:20302]","synonyms":"OKB1,OAT6,FLIPT2,CT2","biotype":"protein_coding","ncbi_id":"85413","summary":"This gene encodes a member of the organic zwitterion transporter protein family which transports carnitine. The encoded protein has also been shown to transport anticancer drugs like bleomycin (PMID: 20037140) successful treatment has been correlated with the level of activity of this transporter in tumor cells. [provided by RefSeq, Dec 2011]","start":110424687,"end":110476641,"strand":-1,"description":"solute carrier family 22 member 16 [Source:HGNC Symbol;Acc:HGNC:20302]"}, {"versioned_ensembl_gene_id":"ENSG00000234108.1","gene_symbol":"AL596276.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80495903,"end":80496233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233545.1","gene_symbol":"CYCSP33","gene_name":"cytochrome c, somatic pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:24407]","synonyms":"HCP33","biotype":"processed_pseudogene","ncbi_id":"221180","summary":null,"start":24400703,"end":24401029,"strand":1,"description":"cytochrome c, somatic pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:24407]"}, {"versioned_ensembl_gene_id":"ENSG00000102699.5","gene_symbol":"PARP4","gene_name":"poly(ADP-ribose) polymerase family member 4 [Source:HGNC Symbol;Acc:HGNC:271]","synonyms":"ADPRTL1,VWA5C,VPARP,VAULT3,p193","biotype":"protein_coding","ncbi_id":"143","summary":"This gene encodes poly(ADP-ribosyl)transferase-like 1 protein, which is capable of catalyzing a poly(ADP-ribosyl)ation reaction. This protein has a catalytic domain which is homologous to that of poly (ADP-ribosyl) transferase, but lacks an N-terminal DNA binding domain which activates the C-terminal catalytic domain of poly (ADP-ribosyl) transferase. Since this protein is not capable of binding DNA directly, its transferase activity may be activated by other factors such as protein-protein interaction mediated by the extensive carboxyl terminus. [provided by RefSeq, Jul 2008]","start":24420926,"end":24512810,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 4 [Source:HGNC Symbol;Acc:HGNC:271]"}, {"versioned_ensembl_gene_id":"ENSG00000279966.2","gene_symbol":"AC008626.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22770375,"end":22770622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234452.5","gene_symbol":"SLC16A12-AS1","gene_name":"SLC16A12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51205]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101926906","summary":null,"start":89456064,"end":89468140,"strand":1,"description":"SLC16A12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51205]"}, {"versioned_ensembl_gene_id":"ENSG00000264265.1","gene_symbol":"LINC01925","gene_name":"long intergenic non-protein coding RNA 1925 [Source:HGNC Symbol;Acc:HGNC:52745]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376854","summary":null,"start":508568,"end":515294,"strand":-1,"description":"long intergenic non-protein coding RNA 1925 [Source:HGNC Symbol;Acc:HGNC:52745]"}, {"versioned_ensembl_gene_id":"ENSG00000239388.8","gene_symbol":"ASB14","gene_name":"ankyrin repeat and SOCS box containing 14 [Source:HGNC Symbol;Acc:HGNC:19766]","synonyms":"DKFZp313L0121","biotype":"protein_coding","ncbi_id":"142686","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and a SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2008]","start":57268347,"end":57292682,"strand":-1,"description":"ankyrin repeat and SOCS box containing 14 [Source:HGNC Symbol;Acc:HGNC:19766]"}, {"versioned_ensembl_gene_id":"ENSG00000184895.7","gene_symbol":"SRY","gene_name":"sex determining region Y [Source:HGNC Symbol;Acc:HGNC:11311]","synonyms":"TDF","biotype":"protein_coding","ncbi_id":"6736","summary":"This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis-determining factor (TDF), which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis (Swyer syndrome); translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome. [provided by RefSeq, Jul 2008]","start":2786855,"end":2787699,"strand":-1,"description":"sex determining region Y [Source:HGNC Symbol;Acc:HGNC:11311]"}, {"versioned_ensembl_gene_id":"ENSG00000281753.1","gene_symbol":"AP001468.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46187390,"end":46191252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275731.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819083,"end":54833565,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000275824.4","gene_symbol":"CCL4","gene_name":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]","synonyms":"MIP-1-beta,MIP-1-beta,LAG1,LAG1,AT744.1,AT744.1,Act-2,Act-2,SCYA4,SCYA4","biotype":"protein_coding","ncbi_id":"6351","summary":"The protein encoded by this gene is a mitogen-inducible monokine and is one of the major HIV-suppressive factors produced by CD8+ T-cells. The encoded protein is secreted and has chemokinetic and inflammatory functions. [provided by RefSeq, Dec 2012]","start":36103979,"end":36106010,"strand":1,"description":"C-C motif chemokine ligand 4 [Source:HGNC Symbol;Acc:HGNC:10630]"}, {"versioned_ensembl_gene_id":"ENSG00000237883.1","gene_symbol":"DGUOK-AS1","gene_name":"DGUOK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43441]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874048","summary":null,"start":73947642,"end":73981441,"strand":-1,"description":"DGUOK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43441]"}, {"versioned_ensembl_gene_id":"ENSG00000261168.1","gene_symbol":"AL592424.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":151130075,"end":151131610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260134.1","gene_symbol":"C1QL1P1","gene_name":"complement C1q like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51809]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480353","summary":null,"start":35574834,"end":35575494,"strand":1,"description":"complement C1q like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51809]"}, {"versioned_ensembl_gene_id":"ENSG00000261046.1","gene_symbol":"C2orf69P1","gene_name":"chromosome 2 open reading frame 69 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727964","summary":null,"start":35552909,"end":35554001,"strand":1,"description":"chromosome 2 open reading frame 69 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51800]"}, {"versioned_ensembl_gene_id":"ENSG00000278795.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54639543,"end":54644657,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000013810.18","gene_symbol":"TACC3","gene_name":"transforming acidic coiled-coil containing protein 3 [Source:HGNC Symbol;Acc:HGNC:11524]","synonyms":"ERIC1","biotype":"protein_coding","ncbi_id":"10460","summary":"This gene encodes a member of the transforming acidic colied-coil protein family. The encoded protein is a motor spindle protein that may play a role in stabilization of the mitotic spindle. This protein may also play a role in growth a differentiation of certain cancer cells. [provided by RefSeq, Nov 2011]","start":1721490,"end":1745176,"strand":1,"description":"transforming acidic coiled-coil containing protein 3 [Source:HGNC Symbol;Acc:HGNC:11524]"}, {"versioned_ensembl_gene_id":"ENSG00000228427.1","gene_symbol":"AL590764.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71183559,"end":71198175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284637.1","gene_symbol":"AC099063.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89203280,"end":89203464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274507.1","gene_symbol":"AL121772.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25251008,"end":25251304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150630.3","gene_symbol":"VEGFC","gene_name":"vascular endothelial growth factor C [Source:HGNC Symbol;Acc:HGNC:12682]","synonyms":"VRP","biotype":"protein_coding","ncbi_id":"7424","summary":"The protein encoded by this gene is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family. The encoded protein promotes angiogenesis and endothelial cell growth, and can also affect the permeability of blood vessels. The proprotein is further cleaved into a fully processed form that can bind and activate VEGFR-2 and VEGFR-3 receptors. [provided by RefSeq, Apr 2014]","start":176683538,"end":176792727,"strand":-1,"description":"vascular endothelial growth factor C [Source:HGNC Symbol;Acc:HGNC:12682]"}, {"versioned_ensembl_gene_id":"ENSG00000261498.1","gene_symbol":"LINC00566","gene_name":"long intergenic non-protein coding RNA 566 [Source:HGNC Symbol;Acc:HGNC:43710]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861547","summary":null,"start":24331450,"end":24337121,"strand":1,"description":"long intergenic non-protein coding RNA 566 [Source:HGNC Symbol;Acc:HGNC:43710]"}, {"versioned_ensembl_gene_id":"ENSG00000054116.11","gene_symbol":"TRAPPC3","gene_name":"trafficking protein particle complex 3 [Source:HGNC Symbol;Acc:HGNC:19942]","synonyms":"BET3","biotype":"protein_coding","ncbi_id":"27095","summary":"This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. The encoded protein participates in the regulation of transport from the endoplasmic reticulum to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":36136570,"end":36156053,"strand":-1,"description":"trafficking protein particle complex 3 [Source:HGNC Symbol;Acc:HGNC:19942]"}, {"versioned_ensembl_gene_id":"ENSG00000106128.18","gene_symbol":"GHRHR","gene_name":"growth hormone releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2692","summary":"This gene encodes a receptor for growth hormone-releasing hormone. Binding of this hormone to the receptor leads to synthesis and release of growth hormone. Mutations in this gene have been associated with isolated growth hormone deficiency (IGHD), also known as Dwarfism of Sindh, a disorder characterized by short stature. [provided by RefSeq, Jun 2010]","start":30938669,"end":30993254,"strand":1,"description":"growth hormone releasing hormone receptor [Source:HGNC Symbol;Acc:HGNC:4266]"}, {"versioned_ensembl_gene_id":"ENSG00000234627.3","gene_symbol":"NUS1P3","gene_name":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30934]","synonyms":"YDD19","biotype":"processed_pseudogene","ncbi_id":"11049","summary":null,"start":24328211,"end":24329072,"strand":1,"description":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30934]"}, {"versioned_ensembl_gene_id":"ENSG00000253471.1","gene_symbol":"AC012574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23707141,"end":23789487,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185652.11","gene_symbol":"NTF3","gene_name":"neurotrophin 3 [Source:HGNC Symbol;Acc:HGNC:8023]","synonyms":"NGF2","biotype":"protein_coding","ncbi_id":"4908","summary":"The protein encoded by this gene is a member of the neurotrophin family, that controls survival and differentiation of mammalian neurons. This protein is closely related to both nerve growth factor and brain-derived neurotrophic factor. It may be involved in the maintenance of the adult nervous system, and may affect development of neurons in the embryo when it is expressed in human placenta. NTF3-deficient mice generated by gene targeting display severe movement defects of the limbs. The mature peptide of this protein is identical in all mammals examined including human, pig, rat and mouse. [provided by RefSeq, Jul 2008]","start":5432112,"end":5521536,"strand":1,"description":"neurotrophin 3 [Source:HGNC Symbol;Acc:HGNC:8023]"}, {"versioned_ensembl_gene_id":"ENSG00000138036.18","gene_symbol":"DYNC2LI1","gene_name":"dynein cytoplasmic 2 light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:24595]","synonyms":"LIC3,DKFZP564A033,D2LIC,CGI-60","biotype":"protein_coding","ncbi_id":"51626","summary":"This gene encodes a protein that is a component of the dynein-2 microtubule motor protein complex that plays a role in the retrograde transport of cargo in primary cilia via the intraflagellar transport system. This gene is ubiquitously expressed and its protein, which localizes to the axoneme and Golgi apparatus, interacts directly with the cytoplasmic dynein 2 heavy chain 1 protein to form part of the multi-protein dynein-2 complex. Mutations in this gene produce defects in the dynein-2 complex which result in several types of ciliopathy including short-rib thoracic dysplasia 15 with polydactyly (SRTD15). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]","start":43774039,"end":43810010,"strand":1,"description":"dynein cytoplasmic 2 light intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:24595]"}, {"versioned_ensembl_gene_id":"ENSG00000260830.1","gene_symbol":"AL135744.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21384292,"end":21384920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079841.18","gene_symbol":"RIMS1","gene_name":"regulating synaptic membrane exocytosis 1 [Source:HGNC Symbol;Acc:HGNC:17282]","synonyms":"RIM1,RIM,RAB3IP2,KIAA0340,CORD7","biotype":"protein_coding","ncbi_id":"22999","summary":"The protein encoded by this gene is a RAS gene superfamily member that regulates synaptic vesicle exocytosis. This gene also plays a role in the regulation of voltage-gated calcium channels during neurotransmitter and insulin release. Mutations have suggested a role cognition and have been identified as the cause of cone-rod dystrophy type 7. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012]","start":71886703,"end":72403143,"strand":1,"description":"regulating synaptic membrane exocytosis 1 [Source:HGNC Symbol;Acc:HGNC:17282]"}, {"versioned_ensembl_gene_id":"ENSG00000257907.2","gene_symbol":"EEF1A1P17","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37890]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401717","summary":null,"start":43659827,"end":43661101,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:37890]"}, {"versioned_ensembl_gene_id":"ENSG00000271508.1","gene_symbol":"AC090525.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43633093,"end":43633281,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224313.6","gene_symbol":"DXO","gene_name":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]","synonyms":"DOM3Z","biotype":"protein_coding","ncbi_id":"1797","summary":"This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. The function of its protein product is unknown, but its ubiquitous expression and conservation in both simple and complex eukaryotes suggests that this may be a housekeeping gene. [provided by RefSeq, Jul 2008]","start":32046253,"end":32048735,"strand":-1,"description":"decapping exoribonuclease [Source:HGNC Symbol;Acc:HGNC:2992]"}, {"versioned_ensembl_gene_id":"ENSG00000183784.6","gene_symbol":"C9orf66","gene_name":"chromosome 9 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:26436]","synonyms":"FLJ31158","biotype":"protein_coding","ncbi_id":"157983","summary":null,"start":212824,"end":215741,"strand":-1,"description":"chromosome 9 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:26436]"}, {"versioned_ensembl_gene_id":"ENSG00000130037.4","gene_symbol":"KCNA5","gene_name":"potassium voltage-gated channel subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:6224]","synonyms":"Kv1.5,HPCN1,HK2","biotype":"protein_coding","ncbi_id":"3741","summary":"Potassium channels represent the most complex class of voltage-gated ino channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12. Defects in this gene are a cause of familial atrial fibrillation type 7 (ATFB7). [provided by RefSeq, May 2012]","start":5043989,"end":5046788,"strand":1,"description":"potassium voltage-gated channel subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:6224]"}, {"versioned_ensembl_gene_id":"ENSG00000229591.1","gene_symbol":"AC006017.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152120001,"end":152121717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277271.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:NCBI gene;Acc:79166]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54707923,"end":54712937,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:NCBI gene;Acc:79166]"}, {"versioned_ensembl_gene_id":"ENSG00000254734.1","gene_symbol":"AC107973.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29713909,"end":29881714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240554.1","gene_symbol":"AL135933.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29725764,"end":29726565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277938.1","gene_symbol":"AL035252.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25229150,"end":25231933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267162.1","gene_symbol":"SDHDP1","gene_name":"succinate dehydrogenase complex subunit D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289186","summary":null,"start":12101997,"end":12102470,"strand":-1,"description":"succinate dehydrogenase complex subunit D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10684]"}, {"versioned_ensembl_gene_id":"ENSG00000273512.1","gene_symbol":"AC022748.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":78749833,"end":78750107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169126.15","gene_symbol":"ARMC4","gene_name":"armadillo repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25583]","synonyms":"FLJ10817,FLJ10376,DKFZP434P1735,CILD23","biotype":"protein_coding","ncbi_id":"55130","summary":"The protein encoded by this gene contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":27812164,"end":27999048,"strand":-1,"description":"armadillo repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:25583]"}, {"versioned_ensembl_gene_id":"ENSG00000257129.1","gene_symbol":"AC126177.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":107910403,"end":107912620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258072.1","gene_symbol":"AC126177.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107903270,"end":107903948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059804.15","gene_symbol":"SLC2A3","gene_name":"solute carrier family 2 member 3 [Source:HGNC Symbol;Acc:HGNC:11007]","synonyms":"GLUT3","biotype":"protein_coding","ncbi_id":"6515","summary":null,"start":7919230,"end":7936275,"strand":-1,"description":"solute carrier family 2 member 3 [Source:HGNC Symbol;Acc:HGNC:11007]"}, {"versioned_ensembl_gene_id":"ENSG00000226999.1","gene_symbol":"AC073325.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45534523,"end":45534681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259366.1","gene_symbol":"AC108449.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29055935,"end":29056685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101307.15","gene_symbol":"SIRPB1","gene_name":"signal regulatory protein beta 1 [Source:HGNC Symbol;Acc:HGNC:15928]","synonyms":"SIRP-BETA-1,CD172b","biotype":"protein_coding","ncbi_id":"10326","summary":"The protein encoded by this gene is a member of the signal-regulatory-protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. This protein was found to interact with TYROBP/DAP12, a protein bearing immunoreceptor tyrosine-based activation motifs. This protein was also reported to participate in the recruitment of tyrosine kinase SYK. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":1563521,"end":1620061,"strand":-1,"description":"signal regulatory protein beta 1 [Source:HGNC Symbol;Acc:HGNC:15928]"}, {"versioned_ensembl_gene_id":"ENSG00000115758.12","gene_symbol":"ODC1","gene_name":"ornithine decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:8109]","synonyms":"ODC","biotype":"protein_coding","ncbi_id":"4953","summary":"This gene encodes the rate-limiting enzyme of the polyamine biosynthesis pathway which catalyzes ornithine to putrescine. The activity level for the enzyme varies in response to growth-promoting stimuli and exhibits a high turnover rate in comparison to other mammalian proteins. Originally localized to both chromosomes 2 and 7, the gene encoding this enzyme has been determined to be located on 2p25, with a pseudogene located on 7q31-qter. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Dec 2013]","start":10439968,"end":10448504,"strand":-1,"description":"ornithine decarboxylase 1 [Source:HGNC Symbol;Acc:HGNC:8109]"}, {"versioned_ensembl_gene_id":"ENSG00000240089.2","gene_symbol":"BMS1P3","gene_name":"BMS1, ribosome biogenesis factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23651]","synonyms":"OTTHUMG00000018662,BMS1LP3,bA96C23.1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"414217","summary":null,"start":86992253,"end":87000435,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23651]"}, {"versioned_ensembl_gene_id":"ENSG00000115514.11","gene_symbol":"TXNDC9","gene_name":"thioredoxin domain containing 9 [Source:HGNC Symbol;Acc:HGNC:24110]","synonyms":"APACD","biotype":"protein_coding","ncbi_id":"10190","summary":"The protein encoded by this gene is a member of the thioredoxin family. The exact function of this protein is not known but it is associated with cell differentiation. [provided by RefSeq, Jul 2008]","start":99318982,"end":99340702,"strand":-1,"description":"thioredoxin domain containing 9 [Source:HGNC Symbol;Acc:HGNC:24110]"}, {"versioned_ensembl_gene_id":"ENSG00000255450.1","gene_symbol":"AC110056.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29275655,"end":29276565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231295.1","gene_symbol":"AC004888.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120746738,"end":120752514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132405.18","gene_symbol":"TBC1D14","gene_name":"TBC1 domain family member 14 [Source:HGNC Symbol;Acc:HGNC:29246]","synonyms":"KIAA1322","biotype":"protein_coding","ncbi_id":"57533","summary":null,"start":6909242,"end":7033118,"strand":1,"description":"TBC1 domain family member 14 [Source:HGNC Symbol;Acc:HGNC:29246]"}, {"versioned_ensembl_gene_id":"ENSG00000257522.5","gene_symbol":"AL133166.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29264381,"end":29381295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184408.9","gene_symbol":"KCND2","gene_name":"potassium voltage-gated channel subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:6238]","synonyms":"RK5,Kv4.2,KIAA1044","biotype":"protein_coding","ncbi_id":"3751","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shal-related subfamily, members of which form voltage-activated A-type potassium ion channels and are prominent in the repolarization phase of the action potential. This member mediates a rapidly inactivating, A-type outward potassium current which is not under the control of the N terminus as it is in Shaker channels. [provided by RefSeq, Jul 2008]","start":120273668,"end":120750331,"strand":1,"description":"potassium voltage-gated channel subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:6238]"}, {"versioned_ensembl_gene_id":"ENSG00000143194.12","gene_symbol":"MAEL","gene_name":"maelstrom spermatogenic transposon silencer [Source:HGNC Symbol;Acc:HGNC:25929]","synonyms":"SPATA35,FLJ14904,CT128","biotype":"protein_coding","ncbi_id":"84944","summary":null,"start":166975582,"end":167022214,"strand":1,"description":"maelstrom spermatogenic transposon silencer [Source:HGNC Symbol;Acc:HGNC:25929]"}, {"versioned_ensembl_gene_id":"ENSG00000148671.13","gene_symbol":"ADIRF","gene_name":"adipogenesis regulatory factor [Source:HGNC Symbol;Acc:HGNC:24043]","synonyms":"C10orf116,APM2,AFRO","biotype":"protein_coding","ncbi_id":"10974","summary":"APM2 gene is exclusively expressed in adipose tissue. Its function is currently unknown. [provided by RefSeq, Jul 2008]","start":86968192,"end":86983934,"strand":1,"description":"adipogenesis regulatory factor [Source:HGNC Symbol;Acc:HGNC:24043]"}, {"versioned_ensembl_gene_id":"ENSG00000062582.13","gene_symbol":"MRPS24","gene_name":"mitochondrial ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:14510]","synonyms":"MRP-S24,HSPC335","biotype":"protein_coding","ncbi_id":"64951","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. A pseudogene corresponding to this gene is found on chromosome 11. Read-through transcription exists between this gene and the upstream upregulator of cell proliferation (URGCP) gene. [provided by RefSeq, Mar 2011]","start":43866558,"end":43869893,"strand":-1,"description":"mitochondrial ribosomal protein S24 [Source:HGNC Symbol;Acc:HGNC:14510]"}, {"versioned_ensembl_gene_id":"ENSG00000253696.2","gene_symbol":"KBTBD11-OT1","gene_name":"KBTBD11 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49147]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104266957","summary":null,"start":1971397,"end":1976478,"strand":1,"description":"KBTBD11 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:49147]"}, {"versioned_ensembl_gene_id":"ENSG00000256940.1","gene_symbol":"AP001453.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64245964,"end":64248217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111271.14","gene_symbol":"ACAD10","gene_name":"acyl-CoA dehydrogenase family member 10 [Source:HGNC Symbol;Acc:HGNC:21597]","synonyms":"MGC5601","biotype":"protein_coding","ncbi_id":"80724","summary":"This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes (ACADs), which participate in the beta-oxidation of fatty acids in mitochondria. The encoded enzyme contains a hydrolase domain at the N-terminal portion, a serine/threonine protein kinase catlytic domain in the central region, and a conserved ACAD domain at the C-terminus. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Nov 2008]","start":111686056,"end":111757107,"strand":1,"description":"acyl-CoA dehydrogenase family member 10 [Source:HGNC Symbol;Acc:HGNC:21597]"}, {"versioned_ensembl_gene_id":"ENSG00000259836.1","gene_symbol":"AGGF1P6","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51744]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481737","summary":null,"start":35489237,"end":35490212,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51744]"}, {"versioned_ensembl_gene_id":"ENSG00000260153.1","gene_symbol":"RARRES2P10","gene_name":"retinoic acid receptor responder 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51742]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481972","summary":null,"start":35485766,"end":35486225,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51742]"}, {"versioned_ensembl_gene_id":"ENSG00000275062.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54723963,"end":54736023,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000181240.13","gene_symbol":"SLC25A41","gene_name":"solute carrier family 25 member 41 [Source:HGNC Symbol;Acc:HGNC:28533]","synonyms":"MGC34725,FLJ40442,APC4","biotype":"protein_coding","ncbi_id":"284427","summary":"SLC25A41 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":6426037,"end":6433779,"strand":-1,"description":"solute carrier family 25 member 41 [Source:HGNC Symbol;Acc:HGNC:28533]"}, {"versioned_ensembl_gene_id":"ENSG00000224708.8","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"G6e,C6orf22","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31699739,"end":31701215,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000258611.2","gene_symbol":"AC087641.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":93065586,"end":93066606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152061.23","gene_symbol":"RABGAP1L","gene_name":"RAB GTPase activating protein 1 like [Source:HGNC Symbol;Acc:HGNC:24663]","synonyms":"TBC1D18,KIAA0471,HHL,FLJ38519","biotype":"protein_coding","ncbi_id":"9910","summary":null,"start":174159410,"end":174995308,"strand":1,"description":"RAB GTPase activating protein 1 like [Source:HGNC Symbol;Acc:HGNC:24663]"}, {"versioned_ensembl_gene_id":"ENSG00000234099.1","gene_symbol":"MTND4P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42223]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873255","summary":null,"start":93922574,"end":93923945,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42223]"}, {"versioned_ensembl_gene_id":"ENSG00000223490.2","gene_symbol":"CHCHD2P5","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39589]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874508","summary":null,"start":93921268,"end":93921667,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39589]"}, {"versioned_ensembl_gene_id":"ENSG00000231165.3","gene_symbol":"TRBV26OR9-2","gene_name":"T-cell receptor beta variable 26/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15485]","synonyms":"TRBV26/OR9-2,TCRBV28S2O,TCRBV28S2,TCRBV26S2","biotype":"TR_V_pseudogene","ncbi_id":"246285","summary":null,"start":33695767,"end":33696059,"strand":1,"description":"T-cell receptor beta variable 26/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15485]"}, {"versioned_ensembl_gene_id":"ENSG00000234518.2","gene_symbol":"PTGES3P1","gene_name":"prostaglandin E synthase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43824]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284672","summary":null,"start":89104285,"end":89104767,"strand":-1,"description":"prostaglandin E synthase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43824]"}, {"versioned_ensembl_gene_id":"ENSG00000228727.8","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"NG23,C6orf26","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31762799,"end":31764851,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000231190.1","gene_symbol":"CR759766.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582310,"end":29582827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233535.1","gene_symbol":"AC003035.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13955393,"end":13963904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272449.1","gene_symbol":"AL139246.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2546465,"end":2547460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116128.10","gene_symbol":"BCL9","gene_name":"B-cell CLL/lymphoma 9 [Source:HGNC Symbol;Acc:HGNC:1008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"607","summary":"BCL9 is associated with B-cell acute lymphoblastic leukemia. It may be a target of translocation in B-cell malignancies with abnormalities of 1q21. Its function is unknown. The overexpression of BCL9 may be of pathogenic significance in B-cell malignancies. [provided by RefSeq, Jul 2008]","start":147541412,"end":147626216,"strand":1,"description":"B-cell CLL/lymphoma 9 [Source:HGNC Symbol;Acc:HGNC:1008]"}, {"versioned_ensembl_gene_id":"ENSG00000187634.11","gene_symbol":"SAMD11","gene_name":"sterile alpha motif domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28706]","synonyms":"MGC45873","biotype":"protein_coding","ncbi_id":"148398","summary":null,"start":923928,"end":944581,"strand":1,"description":"sterile alpha motif domain containing 11 [Source:HGNC Symbol;Acc:HGNC:28706]"}, {"versioned_ensembl_gene_id":"ENSG00000236535.1","gene_symbol":"RC3H1-IT1","gene_name":"RC3H1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41496]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106481790","summary":null,"start":174009267,"end":174016206,"strand":-1,"description":"RC3H1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41496]"}, {"versioned_ensembl_gene_id":"ENSG00000229492.1","gene_symbol":"FO681548.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17418697,"end":17419828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107738.19","gene_symbol":"VSIR","gene_name":"V-set immunoregulatory receptor [Source:HGNC Symbol;Acc:HGNC:30085]","synonyms":"GI24,C10orf54,B7H5,B7-H5,VISTA,SISP1,PD-1H","biotype":"protein_coding","ncbi_id":"64115","summary":null,"start":71747559,"end":71773498,"strand":-1,"description":"V-set immunoregulatory receptor [Source:HGNC Symbol;Acc:HGNC:30085]"}, {"versioned_ensembl_gene_id":"ENSG00000188342.11","gene_symbol":"GTF2F2","gene_name":"general transcription factor IIF subunit 2 [Source:HGNC Symbol;Acc:HGNC:4653]","synonyms":"TFIIF,RAP30,BTF4","biotype":"protein_coding","ncbi_id":"2963","summary":null,"start":45120515,"end":45284909,"strand":1,"description":"general transcription factor IIF subunit 2 [Source:HGNC Symbol;Acc:HGNC:4653]"}, {"versioned_ensembl_gene_id":"ENSG00000275004.3","gene_symbol":"ZNF280B","gene_name":"zinc finger protein 280B [Source:HGNC Symbol;Acc:HGNC:23022]","synonyms":"ZNF632,ZNF279,SUHW2,5'OY11.1","biotype":"protein_coding","ncbi_id":"140883","summary":"The protein encoded by this gene is a transcription factor that upregulates expression of MDM2, which negatively regulates p53 expression. This gene is highly expressed in prostate cancer cells, which leads to a reduction in p53 levels and an increase in growth of the cancer cells. Several transcript variants have been found for this gene, but only one of them is protein-coding. [provided by RefSeq, Jan 2015]","start":22484421,"end":22509154,"strand":-1,"description":"zinc finger protein 280B [Source:HGNC Symbol;Acc:HGNC:23022]"}, {"versioned_ensembl_gene_id":"ENSG00000270195.1","gene_symbol":"AC016773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1712821,"end":1713622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257433.5","gene_symbol":"AC004241.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47706085,"end":47742294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203782.5","gene_symbol":"LOR","gene_name":"loricrin [Source:HGNC Symbol;Acc:HGNC:6663]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4014","summary":"This gene encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases. [provided by RefSeq, Jul 2008]","start":153259700,"end":153262122,"strand":1,"description":"loricrin [Source:HGNC Symbol;Acc:HGNC:6663]"}, {"versioned_ensembl_gene_id":"ENSG00000226296.1","gene_symbol":"AC036101.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53291072,"end":53311065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152102.17","gene_symbol":"FAM168B","gene_name":"family with sequence similarity 168 member B [Source:HGNC Symbol;Acc:HGNC:27016]","synonyms":"MANI,KIAA0280L","biotype":"protein_coding","ncbi_id":"130074","summary":null,"start":131047876,"end":131093460,"strand":-1,"description":"family with sequence similarity 168 member B [Source:HGNC Symbol;Acc:HGNC:27016]"}, {"versioned_ensembl_gene_id":"ENSG00000172771.11","gene_symbol":"EFCAB12","gene_name":"EF-hand calcium binding domain 12 [Source:HGNC Symbol;Acc:HGNC:28061]","synonyms":"C3orf25","biotype":"protein_coding","ncbi_id":"90288","summary":null,"start":129401321,"end":129428651,"strand":-1,"description":"EF-hand calcium binding domain 12 [Source:HGNC Symbol;Acc:HGNC:28061]"}, {"versioned_ensembl_gene_id":"ENSG00000249231.7","gene_symbol":"CASC16","gene_name":"cancer susceptibility 16 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48608]","synonyms":"LOC643714,LINC00918","biotype":"lincRNA","ncbi_id":"643714","summary":null,"start":52552090,"end":52652105,"strand":-1,"description":"cancer susceptibility 16 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48608]"}, {"versioned_ensembl_gene_id":"ENSG00000230779.1","gene_symbol":"AL161636.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153225080,"end":153226006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241656.1","gene_symbol":"UBA52P7","gene_name":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128617","summary":null,"start":115592604,"end":115592983,"strand":-1,"description":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36615]"}, {"versioned_ensembl_gene_id":"ENSG00000205643.10","gene_symbol":"CDPF1","gene_name":"cysteine rich DPF motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33710]","synonyms":"LOC150383,C22orf40","biotype":"protein_coding","ncbi_id":"150383","summary":null,"start":46244011,"end":46250679,"strand":-1,"description":"cysteine rich DPF motif domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33710]"}, {"versioned_ensembl_gene_id":"ENSG00000240215.4","gene_symbol":"TRBV25OR9-2","gene_name":"T-cell receptor beta variable 25/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12206]","synonyms":"TRBV25/OR9-2,TCRBV25S2,TCRBV11S2O,TCRBV11O","biotype":"unprocessed_pseudogene","ncbi_id":"6960","summary":null,"start":33662166,"end":33662663,"strand":1,"description":"T-cell receptor beta variable 25/OR9-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12206]"}, {"versioned_ensembl_gene_id":"ENSG00000272009.1","gene_symbol":"AL121944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28078792,"end":28081130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267187.1","gene_symbol":"AC026898.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47703175,"end":47703745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004478.7","gene_symbol":"FKBP4","gene_name":"FK506 binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3720]","synonyms":"FKBP59,FKBP52","biotype":"protein_coding","ncbi_id":"2288","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds to the immunosuppressants FK506 and rapamycin. It has high structural and functional similarity to FK506-binding protein 1A (FKBP1A), but unlike FKBP1A, this protein does not have immunosuppressant activity when complexed with FK506. It interacts with interferon regulatory factor-4 and plays an important role in immunoregulatory gene expression in B and T lymphocytes. This encoded protein is known to associate with phytanoyl-CoA alpha-hydroxylase. It can also associate with two heat shock proteins (hsp90 and hsp70) and thus may play a role in the intracellular trafficking of hetero-oligomeric forms of the steroid hormone receptors. This protein correlates strongly with adeno-associated virus type 2 vectors (AAV) resulting in a significant increase in AAV-mediated transgene expression in human cell lines. Thus this encoded protein is thought to have important implications for the optimal use of AAV vectors in human gene therapy. The human genome contains several non-transcribed pseudogenes similar to this gene. [provided by RefSeq, Sep 2008]","start":2794953,"end":2805423,"strand":1,"description":"FK506 binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3720]"}, {"versioned_ensembl_gene_id":"ENSG00000280372.1","gene_symbol":"CR382285.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10028361,"end":10029855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111206.12","gene_symbol":"FOXM1","gene_name":"forkhead box M1 [Source:HGNC Symbol;Acc:HGNC:3818]","synonyms":"trident,TGT3,MPP2,MPHOSPH2,INS-1,HNF-3,HFH-11,FKHL16","biotype":"protein_coding","ncbi_id":"2305","summary":"The protein encoded by this gene is a transcriptional activator involved in cell proliferation. The encoded protein is phosphorylated in M phase and regulates the expression of several cell cycle genes, such as cyclin B1 and cyclin D1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":2857681,"end":2877155,"strand":-1,"description":"forkhead box M1 [Source:HGNC Symbol;Acc:HGNC:3818]"}, {"versioned_ensembl_gene_id":"ENSG00000261303.5","gene_symbol":"AC022748.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":78660644,"end":78735495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259555.1","gene_symbol":"AC067863.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78625895,"end":78628193,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256769.1","gene_symbol":"CACNA1C-AS3","gene_name":"CACNA1C antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40117]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478964","summary":null,"start":2603350,"end":2607440,"strand":-1,"description":"CACNA1C antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40117]"}, {"versioned_ensembl_gene_id":"ENSG00000140873.15","gene_symbol":"ADAMTS18","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 18 [Source:HGNC Symbol;Acc:HGNC:17110]","synonyms":"ADAMTS21","biotype":"protein_coding","ncbi_id":"170692","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may regulate hemostatic balance and function as a tumor suppressor. Mutations in this gene may be associated with microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) and cone-rod dystrophy in human patients. [provided by RefSeq, May 2016]","start":77247813,"end":77435114,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 18 [Source:HGNC Symbol;Acc:HGNC:17110]"}, {"versioned_ensembl_gene_id":"ENSG00000155254.12","gene_symbol":"MARVELD1","gene_name":"MARVEL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28674]","synonyms":"MRVLDC1,MGC4415,GB14,FLJ23440,FLJ22343,bA548K23.8","biotype":"protein_coding","ncbi_id":"83742","summary":null,"start":97713173,"end":97718152,"strand":1,"description":"MARVEL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28674]"}, {"versioned_ensembl_gene_id":"ENSG00000172179.11","gene_symbol":"PRL","gene_name":"prolactin [Source:HGNC Symbol;Acc:HGNC:9445]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5617","summary":"This gene encodes the anterior pituitary hormone prolactin. This secreted hormone is a growth regulator for many tissues, including cells of the immune system. It may also play a role in cell survival by suppressing apoptosis, and it is essential for lactation. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Aug 2011]","start":22287244,"end":22297501,"strand":-1,"description":"prolactin [Source:HGNC Symbol;Acc:HGNC:9445]"}, {"versioned_ensembl_gene_id":"ENSG00000226610.1","gene_symbol":"AL662852.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29178191,"end":29179126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182477.5","gene_symbol":"OR2B8P","gene_name":"olfactory receptor family 2 subfamily B member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:13968]","synonyms":"OR2B8,hs6M1-29P","biotype":"unprocessed_pseudogene","ncbi_id":"65944","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":28053228,"end":28054165,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:13968]"}, {"versioned_ensembl_gene_id":"ENSG00000261541.1","gene_symbol":"AC138915.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32454612,"end":32458758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228120.2","gene_symbol":"AP001631.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43159066,"end":43162277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117971.11","gene_symbol":"CHRNB4","gene_name":"cholinergic receptor nicotinic beta 4 subunit [Source:HGNC Symbol;Acc:HGNC:1964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1143","summary":"This gene is found within a conserved gene cluster and encodes one of the beta subunits of the nicotinic acetylcholine receptor (nAChRs) superfamily which form ligand-gated ion channels with a central pore that forms a cation channel. Neuronal nAChRs are pentameric structures that can be either homomeric or heteromeric, with heteromeric structures containing both alpha and beta subunits. Each subunit contains an extracellular amino terminus and four transmembrane domains. Nicotine is one of the agonists that binds to the receptor. Variants in this gene have been associated with nicotine dependence and lung cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2017]","start":78624119,"end":78727754,"strand":-1,"description":"cholinergic receptor nicotinic beta 4 subunit [Source:HGNC Symbol;Acc:HGNC:1964]"}, {"versioned_ensembl_gene_id":"ENSG00000131153.8","gene_symbol":"GINS2","gene_name":"GINS complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24575]","synonyms":"PSF2,Pfs2","biotype":"protein_coding","ncbi_id":"51659","summary":"The yeast heterotetrameric GINS complex is made up of Sld5 (GINS4; MIM 610611), Psf1 (GINS1; MIM 610608), Psf2, and Psf3 (GINS3; MIM 610610). The formation of this complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]). See GINS1 for additional information about the GINS complex.[supplied by OMIM, Mar 2008]","start":85676198,"end":85690073,"strand":-1,"description":"GINS complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24575]"}, {"versioned_ensembl_gene_id":"ENSG00000270296.1","gene_symbol":"STX8P1","gene_name":"syntaxin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49855]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100423046","summary":null,"start":12771351,"end":12771705,"strand":-1,"description":"syntaxin 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49855]"}, {"versioned_ensembl_gene_id":"ENSG00000182087.12","gene_symbol":"TMEM259","gene_name":"transmembrane protein 259 [Source:HGNC Symbol;Acc:HGNC:17039]","synonyms":"MGC4022,MBRL,C19orf6,ASBABP1","biotype":"protein_coding","ncbi_id":"91304","summary":null,"start":1009648,"end":1021179,"strand":-1,"description":"transmembrane protein 259 [Source:HGNC Symbol;Acc:HGNC:17039]"}, {"versioned_ensembl_gene_id":"ENSG00000196693.14","gene_symbol":"ZNF33B","gene_name":"zinc finger protein 33B [Source:HGNC Symbol;Acc:HGNC:13097]","synonyms":"ZNF11B,KOX31,KOX2","biotype":"protein_coding","ncbi_id":"7582","summary":"This gene encodes a member of the zinc finger family of proteins. This gene shows decreased expression in cumulus cells derived from patients undergoing controlled ovarian stimulation. This gene is present in a gene cluster with several related zinc finger genes in the pericentromeric region of chromosome 10. Pseudogenes have been identified on chromosomes 7 and 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":42574185,"end":42638568,"strand":-1,"description":"zinc finger protein 33B [Source:HGNC Symbol;Acc:HGNC:13097]"}, {"versioned_ensembl_gene_id":"ENSG00000172315.5","gene_symbol":"TP53RK","gene_name":"TP53 regulating kinase [Source:HGNC Symbol;Acc:HGNC:16197]","synonyms":"prpk,Nori-2p,dJ101A2.2,C20orf64,BUD32","biotype":"protein_coding","ncbi_id":"112858","summary":null,"start":46684365,"end":46689779,"strand":-1,"description":"TP53 regulating kinase [Source:HGNC Symbol;Acc:HGNC:16197]"}, {"versioned_ensembl_gene_id":"ENSG00000262145.5","gene_symbol":"ATP23","gene_name":"ATP23 metallopeptidase and ATP synthase assembly factor homolog [Source:HGNC Symbol;Acc:HGNC:29452]","synonyms":"XRCC6BP1,KUB3","biotype":"protein_coding","ncbi_id":"91419","summary":"The protein encoded by this gene is amplified in glioblastomas and interacts with the DNA binding subunit of DNA-dependent protein kinase. This kinase is involved in double-strand break repair (DSB), and higher expression of the encoded protein increases the efficiency of DSB. In addition, comparison to orthologous proteins strongly suggests that this protein is a metalloprotease important in the biosynthesis of mitochondrial ATPase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":57941541,"end":57957269,"strand":1,"description":"ATP23 metallopeptidase and ATP synthase assembly factor homolog [Source:HGNC Symbol;Acc:HGNC:29452]"}, {"versioned_ensembl_gene_id":"ENSG00000253805.1","gene_symbol":"AC245164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2033508,"end":2035587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197565.15","gene_symbol":"COL4A6","gene_name":"collagen type IV alpha 6 chain [Source:HGNC Symbol;Acc:HGNC:2208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1288","summary":"This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]","start":108155607,"end":108439497,"strand":-1,"description":"collagen type IV alpha 6 chain [Source:HGNC Symbol;Acc:HGNC:2208]"}, {"versioned_ensembl_gene_id":"ENSG00000262819.1","gene_symbol":"AC084033.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57967058,"end":57968399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280541.1","gene_symbol":"FTCD-AS1","gene_name":"FTCD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40243]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861507","summary":null,"start":46151614,"end":46152647,"strand":1,"description":"FTCD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40243]"}, {"versioned_ensembl_gene_id":"ENSG00000262082.1","gene_symbol":"AC084033.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57983795,"end":57984761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163635.17","gene_symbol":"ATXN7","gene_name":"ataxin 7 [Source:HGNC Symbol;Acc:HGNC:10560]","synonyms":"SCA7,OPCA3,ADCAII","biotype":"protein_coding","ncbi_id":"6314","summary":"The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the 'pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. This locus has been mapped to chromosome 3, and it has been determined that the diseased allele associated with spinocerebellar ataxia-7 contains 37-306 CAG repeats (near the N-terminus), compared to 4-35 in the normal allele. The encoded protein is a component of the SPT3/TAF9/GCN5 acetyltransferase (STAGA) and TBP-free TAF-containing (TFTC) chromatin remodeling complexes, and it thus plays a role in transcriptional regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":63864557,"end":64003462,"strand":1,"description":"ataxin 7 [Source:HGNC Symbol;Acc:HGNC:10560]"}, {"versioned_ensembl_gene_id":"ENSG00000180332.6","gene_symbol":"KCTD4","gene_name":"potassium channel tetramerization domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23227]","synonyms":"bA321C24.3","biotype":"protein_coding","ncbi_id":"386618","summary":null,"start":45192853,"end":45194717,"strand":-1,"description":"potassium channel tetramerization domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23227]"}, {"versioned_ensembl_gene_id":"ENSG00000278268.2","gene_symbol":"MOAP1","gene_name":"modulator of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:16658]","synonyms":"PNMA4,MAP-1","biotype":"protein_coding","ncbi_id":"64112","summary":"The protein encoded by this gene was identified by its interaction with apoptosis regulator BAX protein. This protein contains a Bcl-2 homology 3 (BH3)-like motif, which is required for the association with BAX. When overexpressed, this gene has been shown to mediate caspase-dependent apoptosis. [provided by RefSeq, Jul 2008]","start":93182196,"end":93184928,"strand":-1,"description":"modulator of apoptosis 1 [Source:HGNC Symbol;Acc:HGNC:16658]"}, {"versioned_ensembl_gene_id":"ENSG00000284513.1","gene_symbol":"AC006063.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4960113,"end":4963450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216629.1","gene_symbol":"OR2W4P","gene_name":"olfactory receptor family 2 subfamily W member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15071]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81407","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":27977150,"end":27978075,"strand":1,"description":"olfactory receptor family 2 subfamily W member 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:15071]"}, {"versioned_ensembl_gene_id":"ENSG00000214374.2","gene_symbol":"AL133267.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27965175,"end":27965514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162618.13","gene_symbol":"ADGRL4","gene_name":"adhesion G protein-coupled receptor L4 [Source:HGNC Symbol;Acc:HGNC:20822]","synonyms":"ETL,ELTD1","biotype":"protein_coding","ncbi_id":"64123","summary":null,"start":78889764,"end":79006718,"strand":-1,"description":"adhesion G protein-coupled receptor L4 [Source:HGNC Symbol;Acc:HGNC:20822]"}, {"versioned_ensembl_gene_id":"ENSG00000225238.1","gene_symbol":"Z93015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41472264,"end":41472653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092850.11","gene_symbol":"TEKT2","gene_name":"tektin 2 [Source:HGNC Symbol;Acc:HGNC:11725]","synonyms":"TEKTB1","biotype":"protein_coding","ncbi_id":"27285","summary":"This gene product belongs to the tektin family of proteins. Tektins comprise a family of filament-forming proteins that are coassembled with tubulins to form ciliary and flagellar microtubules. This gene is expressed in the testis and its protein is localized to the flagella of the sperms, indicating that it may play a role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":36084075,"end":36088275,"strand":1,"description":"tektin 2 [Source:HGNC Symbol;Acc:HGNC:11725]"}, {"versioned_ensembl_gene_id":"ENSG00000236920.2","gene_symbol":"AL590727.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98210020,"end":98214683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226207.1","gene_symbol":"AL080316.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97710953,"end":97717197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206417.8","gene_symbol":"H1FX-AS1","gene_name":"H1FX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27953]","synonyms":"FLJ34151,C3orf47","biotype":"antisense_RNA","ncbi_id":"339942","summary":null,"start":129315392,"end":129326225,"strand":1,"description":"H1FX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27953]"}, {"versioned_ensembl_gene_id":"ENSG00000220505.2","gene_symbol":"EIF4EBP2P3","gene_name":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49318]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100190924","summary":null,"start":98179499,"end":98179832,"strand":-1,"description":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49318]"}, {"versioned_ensembl_gene_id":"ENSG00000271860.6","gene_symbol":"AL589740.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97283303,"end":98399872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100216.5","gene_symbol":"TOMM22","gene_name":"translocase of outer mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:18002]","synonyms":"TOM22","biotype":"protein_coding","ncbi_id":"56993","summary":"The protein encoded by this gene is an integral membrane protein of the mitochondrial outer membrane. The encoded protein interacts with TOMM20 and TOMM40, and forms a complex with several other proteins to import cytosolic preproteins into the mitochondrion. [provided by RefSeq, Jul 2008]","start":38681948,"end":38685421,"strand":1,"description":"translocase of outer mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:18002]"}, {"versioned_ensembl_gene_id":"ENSG00000229411.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29899031,"end":29899890,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000277104.4","gene_symbol":"TADA2A","gene_name":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]","synonyms":"hADA2,ADA2A,ADA2,TADA2L","biotype":"protein_coding","ncbi_id":"6871","summary":"Many DNA-binding transcriptional activator proteins enhance the initiation rate of RNA polymerase II-mediated gene transcription by interacting functionally with the general transcription machinery bound at the basal promoter. Adaptor proteins are usually required for this activation, possibly to acetylate and destabilize nucleosomes, thereby relieving chromatin constraints at the promoter. The protein encoded by this gene is a transcriptional activator adaptor and has been found to be part of the PCAF histone acetylase complex. Several alternatively spliced transcript variants encoding different isoforms of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2009]","start":37411498,"end":37484368,"strand":1,"description":"transcriptional adaptor 2A [Source:HGNC Symbol;Acc:HGNC:11531]"}, {"versioned_ensembl_gene_id":"ENSG00000236441.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29897789,"end":29898155,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000271579.1","gene_symbol":"AC078880.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115299588,"end":115300708,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283761.1","gene_symbol":"AC118553.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99970011,"end":100083321,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250523.1","gene_symbol":"AC093909.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188630924,"end":188631747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225150.1","gene_symbol":"AL662857.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29225912,"end":29226842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273464.1","gene_symbol":"AP000238.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29657406,"end":29657831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112715.21","gene_symbol":"VEGFA","gene_name":"vascular endothelial growth factor A [Source:HGNC Symbol;Acc:HGNC:12680]","synonyms":"VPF,VEGF-A,VEGF","biotype":"protein_coding","ncbi_id":"7422","summary":"This gene is a member of the PDGF/VEGF growth factor family. It encodes a heparin-binding protein, which exists as a disulfide-linked homodimer. This growth factor induces proliferation and migration of vascular endothelial cells, and is essential for both physiological and pathological angiogenesis. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation. This gene is upregulated in many known tumors and its expression is correlated with tumor stage and progression. Elevated levels of this protein are found in patients with POEMS syndrome, also known as Crow-Fukase syndrome. Allelic variants of this gene have been associated with microvascular complications of diabetes 1 (MVCD1) and atherosclerosis. Alternatively spliced transcript variants encoding different isoforms have been described. There is also evidence for alternative translation initiation from upstream non-AUG (CUG) codons resulting in additional isoforms. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is antiangiogenic. Expression of some isoforms derived from the AUG start codon is regulated by a small upstream open reading frame, which is located within an internal ribosome entry site. The levels of VEGF are increased during infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), thus promoting inflammation by facilitating recruitment of inflammatory cells, and by increasing the level of angiopoietin II (Ang II), one of two products of the SARS-CoV-2 binding target, angiotensin-converting enzyme 2 (ACE2). In turn, Ang II facilitates the elevation of VEGF, thus forming a vicious cycle in the release of inflammatory cytokines. [provided by RefSeq, Jun 2020]","start":43770184,"end":43786487,"strand":1,"description":"vascular endothelial growth factor A [Source:HGNC Symbol;Acc:HGNC:12680]"}, {"versioned_ensembl_gene_id":"ENSG00000235419.5","gene_symbol":"AC010149.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230520594,"end":230580006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215533.8","gene_symbol":"LINC00189","gene_name":"long intergenic non-protein coding RNA 189 [Source:HGNC Symbol;Acc:HGNC:18461]","synonyms":"NCRNA00189,C21orf109","biotype":"sense_overlapping","ncbi_id":"193629","summary":null,"start":29193480,"end":29288205,"strand":1,"description":"long intergenic non-protein coding RNA 189 [Source:HGNC Symbol;Acc:HGNC:18461]"}, {"versioned_ensembl_gene_id":"ENSG00000241794.1","gene_symbol":"SPRR2A","gene_name":"small proline rich protein 2A [Source:HGNC Symbol;Acc:HGNC:11261]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6700","summary":null,"start":153056113,"end":153057537,"strand":-1,"description":"small proline rich protein 2A [Source:HGNC Symbol;Acc:HGNC:11261]"}, {"versioned_ensembl_gene_id":"ENSG00000130177.14","gene_symbol":"CDC16","gene_name":"cell division cycle 16 [Source:HGNC Symbol;Acc:HGNC:1720]","synonyms":"CUT9,APC6,ANAPC6","biotype":"protein_coding","ncbi_id":"8881","summary":"The protein encoded by this gene functions as a protein ubiquitin ligase and is a component of the multiprotein APC complex. The APC complex is a cyclin degradation system that governs exit from mitosis by targeting cell cycle proteins for degredation by the 26S proteasome. Each component protein of the APC complex is highly conserved among eukaryotic organisms. This protein, and other APC complex proteins, contain a tetratricopeptide repeat (TPR) domain; a protein domain that is often involved in protein-protein interactions and the assembly of multiprotein complexes. Multiple alternatively spliced transcript variants, encoding distinct proteins, have been identified. [provided by RefSeq, Jan 2016]","start":114234887,"end":114272723,"strand":1,"description":"cell division cycle 16 [Source:HGNC Symbol;Acc:HGNC:1720]"}, {"versioned_ensembl_gene_id":"ENSG00000168575.9","gene_symbol":"SLC20A2","gene_name":"solute carrier family 20 member 2 [Source:HGNC Symbol;Acc:HGNC:10947]","synonyms":"Glvr-2,Ram-1,PiT-2,MLVAR,GLVR2","biotype":"protein_coding","ncbi_id":"6575","summary":"This gene encodes a member of the inorganic phosphate transporter family. The encoded protein is a type 3 sodium-dependent phosphate symporter that plays an important role in phosphate homeostasis by mediating cellular phosphate uptake. The encoded protein also confers susceptibility to viral infection as a gamma-retroviral receptor. Mutations in this gene may play a role in familial idiopathic basal ganglia calcification. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]","start":42416475,"end":42541926,"strand":-1,"description":"solute carrier family 20 member 2 [Source:HGNC Symbol;Acc:HGNC:10947]"}, {"versioned_ensembl_gene_id":"ENSG00000267761.3","gene_symbol":"MIR4527HG","gene_name":"MIR4527 host gene [Source:HGNC Symbol;Acc:HGNC:31724]","synonyms":null,"biotype":"lincRNA","ncbi_id":"110175910","summary":null,"start":47285725,"end":47594550,"strand":1,"description":"MIR4527 host gene [Source:HGNC Symbol;Acc:HGNC:31724]"}, {"versioned_ensembl_gene_id":"ENSG00000110768.11","gene_symbol":"GTF2H1","gene_name":"general transcription factor IIH subunit 1 [Source:HGNC Symbol;Acc:HGNC:4655]","synonyms":"TFIIH,P62,BTF2","biotype":"protein_coding","ncbi_id":"2965","summary":null,"start":18322295,"end":18367044,"strand":1,"description":"general transcription factor IIH subunit 1 [Source:HGNC Symbol;Acc:HGNC:4655]"}, {"versioned_ensembl_gene_id":"ENSG00000282511.1","gene_symbol":"CLUHP10","gene_name":"clustered mitochondria homolog pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51574]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107161230","summary":null,"start":75629993,"end":75634057,"strand":1,"description":"clustered mitochondria homolog pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:51574]"}, {"versioned_ensembl_gene_id":"ENSG00000253392.2","gene_symbol":"AC119403.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2915146,"end":2926807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280521.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000260427.1","gene_symbol":"AGGF1P9","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51746]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127958","summary":null,"start":35347385,"end":35348297,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51746]"}, {"versioned_ensembl_gene_id":"ENSG00000276657.2","gene_symbol":"PYCR3","gene_name":"pyrroline-5-carboxylate reductase 3 [Source:HGNC Symbol;Acc:HGNC:25846]","synonyms":"PYCRL,FLJ13852","biotype":"protein_coding","ncbi_id":"65263","summary":"This gene encodes a protein that belongs to the pyrroline-5-carboxylate reductase family of enzymes. Members of this family catalyze the final step in proline biosynthesis, converting pyrroline-5-carboxylate to proline. Glutamate and ornithine are precursors in the synthesis of proline. The protein encoded by this gene is a cytoplasmic enzyme involved in the biosynthesis of proline from ornithine. [provided by RefSeq, Aug 2016]","start":143603913,"end":143609773,"strand":-1,"description":"pyrroline-5-carboxylate reductase 3 [Source:HGNC Symbol;Acc:HGNC:25846]"}, {"versioned_ensembl_gene_id":"ENSG00000121858.10","gene_symbol":"TNFSF10","gene_name":"TNF superfamily member 10 [Source:HGNC Symbol;Acc:HGNC:11925]","synonyms":"TRAIL,TL2,CD253,Apo-2L","biotype":"protein_coding","ncbi_id":"8743","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein preferentially induces apoptosis in transformed and tumor cells, but does not appear to kill normal cells although it is expressed at a significant level in most normal tissues. This protein binds to several members of TNF receptor superfamily including TNFRSF10A/TRAILR1, TNFRSF10B/TRAILR2, TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and possibly also to TNFRSF11B/OPG. The activity of this protein may be modulated by binding to the decoy receptors TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and TNFRSF11B/OPG that cannot induce apoptosis. The binding of this protein to its receptors has been shown to trigger the activation of MAPK8/JNK, caspase 8, and caspase 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":172505508,"end":172523507,"strand":-1,"description":"TNF superfamily member 10 [Source:HGNC Symbol;Acc:HGNC:11925]"}, {"versioned_ensembl_gene_id":"ENSG00000163611.11","gene_symbol":"SPICE1","gene_name":"spindle and centriole associated protein 1 [Source:HGNC Symbol;Acc:HGNC:25083]","synonyms":"SPICE,CCDC52","biotype":"protein_coding","ncbi_id":"152185","summary":null,"start":113442718,"end":113515187,"strand":-1,"description":"spindle and centriole associated protein 1 [Source:HGNC Symbol;Acc:HGNC:25083]"}, {"versioned_ensembl_gene_id":"ENSG00000236138.4","gene_symbol":"DUX4L26","gene_name":"double homeobox 4 like 26 [Source:HGNC Symbol;Acc:HGNC:50807]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996350","summary":null,"start":75668931,"end":75670185,"strand":1,"description":"double homeobox 4 like 26 [Source:HGNC Symbol;Acc:HGNC:50807]"}, {"versioned_ensembl_gene_id":"ENSG00000262152.6","gene_symbol":"LINC00514","gene_name":"long intergenic non-protein coding RNA 514 [Source:HGNC Symbol;Acc:HGNC:27549]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283875","summary":null,"start":2988961,"end":2994509,"strand":1,"description":"long intergenic non-protein coding RNA 514 [Source:HGNC Symbol;Acc:HGNC:27549]"}, {"versioned_ensembl_gene_id":"ENSG00000279278.1","gene_symbol":"AC245060.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22264601,"end":22273020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170142.11","gene_symbol":"UBE2E1","gene_name":"ubiquitin conjugating enzyme E2 E1 [Source:HGNC Symbol;Acc:HGNC:12477]","synonyms":"UbcH6","biotype":"protein_coding","ncbi_id":"7324","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":23805903,"end":23891316,"strand":1,"description":"ubiquitin conjugating enzyme E2 E1 [Source:HGNC Symbol;Acc:HGNC:12477]"}, {"versioned_ensembl_gene_id":"ENSG00000231559.1","gene_symbol":"Z95118.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108817680,"end":108817926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228817.4","gene_symbol":"BACH1-IT2","gene_name":"BACH1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:40007]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874322","summary":null,"start":29370497,"end":29373709,"strand":1,"description":"BACH1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:40007]"}, {"versioned_ensembl_gene_id":"ENSG00000219565.2","gene_symbol":"ZNF259P1","gene_name":"zinc finger protein 259 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13052]","synonyms":"ZNF259P,354J5","biotype":"transcribed_processed_pseudogene","ncbi_id":"442240","summary":null,"start":108782126,"end":108787053,"strand":-1,"description":"zinc finger protein 259 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13052]"}, {"versioned_ensembl_gene_id":"ENSG00000234262.1","gene_symbol":"AL356867.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153023962,"end":153024260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261071.1","gene_symbol":"AL441883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13614111,"end":13615155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256041.1","gene_symbol":"AP001858.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63032503,"end":63033103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065923.9","gene_symbol":"SLC9A7","gene_name":"solute carrier family 9 member A7 [Source:HGNC Symbol;Acc:HGNC:17123]","synonyms":"NHE7","biotype":"protein_coding","ncbi_id":"84679","summary":"This gene encodes a sodium and potassium/ proton antiporter that is a member of the solute carrier family 9 protein family. The encoded protein is primarily localized to the trans-Golgi network and is involved in maintaining pH homeostasis in organelles along the secretory and endocytic pathways. This protein may enhance cell growth of certain breast tumors. This gene is part of a gene cluster on chromosome Xp11.23. A pseudogene of this gene is found on chromosome 12. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":46599252,"end":46759172,"strand":-1,"description":"solute carrier family 9 member A7 [Source:HGNC Symbol;Acc:HGNC:17123]"}, {"versioned_ensembl_gene_id":"ENSG00000227853.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31649071,"end":31651461,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000244571.1","gene_symbol":"RPS6P4","gene_name":"ribosomal protein S6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36548]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131548","summary":null,"start":163115429,"end":163116186,"strand":1,"description":"ribosomal protein S6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36548]"}, {"versioned_ensembl_gene_id":"ENSG00000141437.8","gene_symbol":"SLC25A52","gene_name":"solute carrier family 25 member 52 [Source:HGNC Symbol;Acc:HGNC:23324]","synonyms":"MCART2","biotype":"protein_coding","ncbi_id":"147407","summary":"This gene is similar to the mitochondrial carrier triple repeat 1 gene on chromosome 9. The gene is intronless and may be an evolving pseudogene; however, it is transcribed and it contains a full-length coding region so it is currently classified as a protein-coding locus. [provided by RefSeq, Jul 2008]","start":31759562,"end":31760880,"strand":-1,"description":"solute carrier family 25 member 52 [Source:HGNC Symbol;Acc:HGNC:23324]"}, {"versioned_ensembl_gene_id":"ENSG00000241369.5","gene_symbol":"LINC01192","gene_name":"long intergenic non-protein coding RNA 1192 [Source:HGNC Symbol;Acc:HGNC:37197]","synonyms":"CT64","biotype":"lincRNA","ncbi_id":"647107","summary":null,"start":163127923,"end":163361563,"strand":-1,"description":"long intergenic non-protein coding RNA 1192 [Source:HGNC Symbol;Acc:HGNC:37197]"}, {"versioned_ensembl_gene_id":"ENSG00000241644.2","gene_symbol":"INMT","gene_name":"indolethylamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:6069]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11185","summary":"N-methylation of endogenous and xenobiotic compounds is a major method by which they are degraded. This gene encodes an enzyme that N-methylates indoles such as tryptamine. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream MINDY4 (aka FAM188B) gene. In rodents and other mammals such as cetartiodactyla this gene is in the opposite orientation compared to its orientation in human and other primates and this gene appears to have been lost in carnivora and chiroptera. [provided by RefSeq, Jul 2019]","start":30697985,"end":30757602,"strand":1,"description":"indolethylamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:6069]"}, {"versioned_ensembl_gene_id":"ENSG00000231676.4","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"hs6M1-6,dJ80I19.4,OR6-8","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29169965,"end":29171236,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000182247.9","gene_symbol":"UBE2E2","gene_name":"ubiquitin conjugating enzyme E2 E2 [Source:HGNC Symbol;Acc:HGNC:12478]","synonyms":"UbcH8,FLJ25157","biotype":"protein_coding","ncbi_id":"7325","summary":null,"start":23203020,"end":23591793,"strand":1,"description":"ubiquitin conjugating enzyme E2 E2 [Source:HGNC Symbol;Acc:HGNC:12478]"}, {"versioned_ensembl_gene_id":"ENSG00000101825.7","gene_symbol":"MXRA5","gene_name":"matrix remodeling associated 5 [Source:HGNC Symbol;Acc:HGNC:7539]","synonyms":"DKFZp564I1922","biotype":"protein_coding","ncbi_id":"25878","summary":"This gene encodes one of the matrix-remodelling associated proteins. This protein contains 7 leucine-rich repeats and 12 immunoglobulin-like C2-type domains related to perlecan. This gene has a pseudogene on chromosome Y. [provided by RefSeq, Mar 2010]","start":3308565,"end":3346641,"strand":-1,"description":"matrix remodeling associated 5 [Source:HGNC Symbol;Acc:HGNC:7539]"}, {"versioned_ensembl_gene_id":"ENSG00000241073.1","gene_symbol":"AC093019.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100057990,"end":100084471,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272264.1","gene_symbol":"AC009686.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80032724,"end":80033300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254205.1","gene_symbol":"AC009686.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80122852,"end":80127670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172000.7","gene_symbol":"ZNF556","gene_name":"zinc finger protein 556 [Source:HGNC Symbol;Acc:HGNC:25669]","synonyms":"FLJ11637","biotype":"protein_coding","ncbi_id":"80032","summary":null,"start":2867335,"end":2883445,"strand":1,"description":"zinc finger protein 556 [Source:HGNC Symbol;Acc:HGNC:25669]"}, {"versioned_ensembl_gene_id":"ENSG00000259627.1","gene_symbol":"AC079328.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63070025,"end":63071911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259498.1","gene_symbol":"AC079328.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63046034,"end":63049387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169118.17","gene_symbol":"CSNK1G1","gene_name":"casein kinase 1 gamma 1 [Source:HGNC Symbol;Acc:HGNC:2454]","synonyms":"CK1gamma1","biotype":"protein_coding","ncbi_id":"53944","summary":"This gene encodes a member of the casein kinase I gene family. This family is comprised of serine/threonine kinases that phosphorylate acidic proteins such as caseins. The encoded kinase plays a role in cell cycle checkpoint arrest in response to stalled replication forks by phosphorylating Claspin. A mutation in this gene may be associated with non-syndromic early-onset epilepsy (NSEOE). [provided by RefSeq, Jul 2016]","start":64165517,"end":64356259,"strand":-1,"description":"casein kinase 1 gamma 1 [Source:HGNC Symbol;Acc:HGNC:2454]"}, {"versioned_ensembl_gene_id":"ENSG00000117620.14","gene_symbol":"SLC35A3","gene_name":"solute carrier family 35 member A3 [Source:HGNC Symbol;Acc:HGNC:11023]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23443","summary":"This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. In cattle, a missense mutation in this gene causes complex vertebral malformation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":99969351,"end":100035637,"strand":1,"description":"solute carrier family 35 member A3 [Source:HGNC Symbol;Acc:HGNC:11023]"}, {"versioned_ensembl_gene_id":"ENSG00000076554.15","gene_symbol":"TPD52","gene_name":"tumor protein D52 [Source:HGNC Symbol;Acc:HGNC:12005]","synonyms":"N8L,hD52,D52","biotype":"protein_coding","ncbi_id":"7163","summary":null,"start":80034745,"end":80231232,"strand":-1,"description":"tumor protein D52 [Source:HGNC Symbol;Acc:HGNC:12005]"}, {"versioned_ensembl_gene_id":"ENSG00000254959.6","gene_symbol":"INMT-MINDY4","gene_name":"INMT-MINDY4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41995]","synonyms":"INMT-FAM188B","biotype":"protein_coding","ncbi_id":"100526825","summary":"This locus represents rare but naturally occurring read-through transcription between the INMT (indolethylamine N-methyltransferase) and FAM188B (family with sequence similarity 188, member B) genes on chromosome 7. The read-through transcript is unlikely to produce a protein because it is a nonsense-mediated mRNA decay (NMD) candidate based on translation from the supported INMT start codon. [provided by RefSeq, Nov 2010]","start":30752137,"end":30892081,"strand":1,"description":"INMT-MINDY4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41995]"}, {"versioned_ensembl_gene_id":"ENSG00000110900.14","gene_symbol":"TSPAN11","gene_name":"tetraspanin 11 [Source:HGNC Symbol;Acc:HGNC:30795]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441631","summary":null,"start":30926428,"end":30996599,"strand":1,"description":"tetraspanin 11 [Source:HGNC Symbol;Acc:HGNC:30795]"}, {"versioned_ensembl_gene_id":"ENSG00000235148.2","gene_symbol":"HMGB3P23","gene_name":"high mobility group box 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39315]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288563","summary":null,"start":31644576,"end":31645160,"strand":-1,"description":"high mobility group box 3 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39315]"}, {"versioned_ensembl_gene_id":"ENSG00000270646.1","gene_symbol":"AL670379.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120976668,"end":120976919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241917.1","gene_symbol":"AC084398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101936216,"end":101936674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249859.9","gene_symbol":"PVT1","gene_name":"Pvt1 oncogene (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:9709]","synonyms":"onco-lncRNA-100,NCRNA00079,LINC00079","biotype":"lincRNA","ncbi_id":"5820","summary":"This gene represents a long non-coding RNA locus that has been identified as a candidate oncogene. Increased copy number and overexpression of this gene are associated with many types of cancers including breast and ovarian cancers, acute myeloid leukemia and Hodgkin lymphoma. Allelic variants of this gene are also associated with end-stage renal disease attributed to type 1 diabetes. Consistent with its association with various types of cancer, transcription of this gene is regulated by the tumor suppressor p53 through a canonical p53-binding site, and it has been implicated in regulating levels of the proto-oncogene MYC to promote tumorigenesis. [provided by RefSeq, Sep 2015]","start":127794533,"end":128101253,"strand":1,"description":"Pvt1 oncogene (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:9709]"}, {"versioned_ensembl_gene_id":"ENSG00000225171.2","gene_symbol":"DUTP6","gene_name":"deoxyuridine triphosphatase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39519]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873912","summary":null,"start":166868748,"end":166869209,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39519]"}, {"versioned_ensembl_gene_id":"ENSG00000213487.3","gene_symbol":"ASS1P4","gene_name":"argininosuccinate synthetase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:767]","synonyms":"ASSP4","biotype":"processed_pseudogene","ncbi_id":"449","summary":null,"start":3367149,"end":3368382,"strand":1,"description":"argininosuccinate synthetase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:767]"}, {"versioned_ensembl_gene_id":"ENSG00000228973.1","gene_symbol":"AC009955.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219625059,"end":219626693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102882.11","gene_symbol":"MAPK3","gene_name":"mitogen-activated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:6877]","synonyms":"PRKM3,p44mapk,p44erk1,ERK1","biotype":"protein_coding","ncbi_id":"5595","summary":"The protein encoded by this gene is a member of the MAP kinase family. MAP kinases, also known as extracellular signal-regulated kinases (ERKs), act in a signaling cascade that regulates various cellular processes such as proliferation, differentiation, and cell cycle progression in response to a variety of extracellular signals. This kinase is activated by upstream kinases, resulting in its translocation to the nucleus where it phosphorylates nuclear targets. Alternatively spliced transcript variants encoding different protein isoforms have been described. [provided by RefSeq, Jul 2008]","start":30114105,"end":30123506,"strand":-1,"description":"mitogen-activated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:6877]"}, {"versioned_ensembl_gene_id":"ENSG00000224649.1","gene_symbol":"AF124730.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29182027,"end":29187795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267398.1","gene_symbol":"AC006130.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2874950,"end":2875592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091181.19","gene_symbol":"IL5RA","gene_name":"interleukin 5 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6017]","synonyms":"IL5R,CDw125,CD125","biotype":"protein_coding","ncbi_id":"3568","summary":"The protein encoded by this gene is an interleukin 5 specific subunit of a heterodimeric cytokine receptor. The receptor is comprised of a ligand specific alpha subunit and a signal transducing beta subunit shared by the receptors for interleukin 3 (IL3), colony stimulating factor 2 (CSF2/GM-CSF), and interleukin 5 (IL5). The binding of this protein to IL5 depends on the beta subunit. The beta subunit is activated by the ligand binding, and is required for the biological activities of IL5. This protein has been found to interact with syndecan binding protein (syntenin), which is required for IL5 mediated activation of the transcription factor SOX4. Several alternatively spliced transcript variants encoding four distinct isoforms have been reported. [provided by RefSeq, Jul 2011]","start":3066326,"end":3126613,"strand":-1,"description":"interleukin 5 receptor subunit alpha [Source:HGNC Symbol;Acc:HGNC:6017]"}, {"versioned_ensembl_gene_id":"ENSG00000047249.17","gene_symbol":"ATP6V1H","gene_name":"ATPase H+ transporting V1 subunit H [Source:HGNC Symbol;Acc:HGNC:18303]","synonyms":"CGI-11,VMA13,SFDbeta,SFDalpha,SFD","biotype":"protein_coding","ncbi_id":"51606","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular organelles. V-ATPase-dependent organelle acidification is necessary for multiple processes including protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. The encoded protein is the regulatory H subunit of the V1 domain of V-ATPase, which is required for catalysis of ATP but not the assembly of V-ATPase. Decreased expression of this gene may play a role in the development of type 2 diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":53715557,"end":53843558,"strand":-1,"description":"ATPase H+ transporting V1 subunit H [Source:HGNC Symbol;Acc:HGNC:18303]"}, {"versioned_ensembl_gene_id":"ENSG00000236188.1","gene_symbol":"PRKX-AS1","gene_name":"PRKX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40479]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873944","summary":null,"start":3659487,"end":3668192,"strand":1,"description":"PRKX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40479]"}, {"versioned_ensembl_gene_id":"ENSG00000186897.4","gene_symbol":"C1QL4","gene_name":"complement C1q like 4 [Source:HGNC Symbol;Acc:HGNC:31416]","synonyms":"CTRP11,C1QTNF11","biotype":"protein_coding","ncbi_id":"338761","summary":null,"start":49332411,"end":49337188,"strand":-1,"description":"complement C1q like 4 [Source:HGNC Symbol;Acc:HGNC:31416]"}, {"versioned_ensembl_gene_id":"ENSG00000183943.5","gene_symbol":"PRKX","gene_name":"protein kinase, X-linked [Source:HGNC Symbol;Acc:HGNC:9441]","synonyms":"PKX1","biotype":"protein_coding","ncbi_id":"5613","summary":"This gene encodes a serine threonine protein kinase that has similarity to the catalytic subunit of cyclic AMP dependent protein kinases. The encoded protein is developmentally regulated and may be involved in renal epithelial morphogenesis. This protein may also be involved in macrophage and granulocyte maturation. Abnormal recombination between this gene and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females. Pseudogenes of this gene are found on chromosomes X, 15 and Y. [provided by RefSeq, Feb 2010]","start":3604370,"end":3713608,"strand":-1,"description":"protein kinase, X-linked [Source:HGNC Symbol;Acc:HGNC:9441]"}, {"versioned_ensembl_gene_id":"ENSG00000163794.6","gene_symbol":"UCN","gene_name":"urocortin [Source:HGNC Symbol;Acc:HGNC:12516]","synonyms":"UROC,UI","biotype":"protein_coding","ncbi_id":"7349","summary":"This gene encodes a member of the sauvagine/corticotropin-releasing factor/urotensin I family. The encoded preproprotein is proteolytically processed to generate the mature peptide, an endogenous ligand for both corticotropin-releasing factor receptor 1 and corticotropin-releasing factor receptor 2. In the brain this peptide may be responsible for the effects of stress on appetite. This peptide may also play a role in mood disorders, neurodegeneration, and skeletal system disorders. In spite of the gene family name similarity, the product of this gene has no sequence similarity to urotensin-2. [provided by RefSeq, Feb 2016]","start":27307400,"end":27308445,"strand":-1,"description":"urocortin [Source:HGNC Symbol;Acc:HGNC:12516]"}, {"versioned_ensembl_gene_id":"ENSG00000127423.10","gene_symbol":"AUNIP","gene_name":"aurora kinase A and ninein interacting protein [Source:HGNC Symbol;Acc:HGNC:28363]","synonyms":"MGC2603,C1orf135,AIBp","biotype":"protein_coding","ncbi_id":"79000","summary":null,"start":25831913,"end":25859458,"strand":-1,"description":"aurora kinase A and ninein interacting protein [Source:HGNC Symbol;Acc:HGNC:28363]"}, {"versioned_ensembl_gene_id":"ENSG00000228171.1","gene_symbol":"AC121251.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23389661,"end":23389909,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175063.16","gene_symbol":"UBE2C","gene_name":"ubiquitin conjugating enzyme E2 C [Source:HGNC Symbol;Acc:HGNC:15937]","synonyms":"UBCH10","biotype":"protein_coding","ncbi_id":"11065","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, ubiquitin-conjugating enzymes, and ubiquitin-protein ligases. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein is required for the destruction of mitotic cyclins and for cell cycle progression, and may be involved in cancer progression. Multiple transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene have been defined on chromosomes 4, 14, 15, 18, and 19. [provided by RefSeq, Aug 2013]","start":45812576,"end":45816957,"strand":1,"description":"ubiquitin conjugating enzyme E2 C [Source:HGNC Symbol;Acc:HGNC:15937]"}, {"versioned_ensembl_gene_id":"ENSG00000173486.12","gene_symbol":"FKBP2","gene_name":"FK506 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3718]","synonyms":"PPIase,FKBP-13","biotype":"protein_coding","ncbi_id":"2286","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It is thought to function as an ER chaperone and may also act as a component of membrane cytoskeletal scaffolds. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2008]","start":64241003,"end":64244132,"strand":1,"description":"FK506 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3718]"}, {"versioned_ensembl_gene_id":"ENSG00000234176.1","gene_symbol":"HSPA8P1","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5245]","synonyms":"HSPAP1","biotype":"processed_pseudogene","ncbi_id":"3314","summary":null,"start":121203182,"end":121205014,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5245]"}, {"versioned_ensembl_gene_id":"ENSG00000223904.2","gene_symbol":"HMGB1P12","gene_name":"high mobility group box 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:13317]","synonyms":"HMGB1L12","biotype":"processed_pseudogene","ncbi_id":"100129723","summary":null,"start":111434427,"end":111435024,"strand":1,"description":"high mobility group box 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:13317]"}, {"versioned_ensembl_gene_id":"ENSG00000267221.2","gene_symbol":"C17orf113","gene_name":"chromosome 17 open reading frame 113 [Source:HGNC Symbol;Acc:HGNC:53437]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42038232,"end":42050614,"strand":-1,"description":"chromosome 17 open reading frame 113 [Source:HGNC Symbol;Acc:HGNC:53437]"}, {"versioned_ensembl_gene_id":"ENSG00000213041.4","gene_symbol":"AC093422.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205202191,"end":205202742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175471.19","gene_symbol":"MCTP1","gene_name":"multiple C2 and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26183]","synonyms":"FLJ22344","biotype":"protein_coding","ncbi_id":"79772","summary":null,"start":94703741,"end":95284575,"strand":-1,"description":"multiple C2 and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26183]"}, {"versioned_ensembl_gene_id":"ENSG00000256204.1","gene_symbol":"AC073862.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130977562,"end":130978768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266190.1","gene_symbol":"AC090287.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28021668,"end":28022265,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282281.1","gene_symbol":"IGHV3-21","gene_name":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28444","summary":null,"start":106235833,"end":106236365,"strand":-1,"description":"immunoglobulin heavy variable 3-21 [Source:HGNC Symbol;Acc:HGNC:5586]"}, {"versioned_ensembl_gene_id":"ENSG00000130675.14","gene_symbol":"MNX1","gene_name":"motor neuron and pancreas homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4979]","synonyms":"SCRA1,HOXHB9,HLXB9,HB9","biotype":"protein_coding","ncbi_id":"3110","summary":"This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":156994051,"end":157010651,"strand":-1,"description":"motor neuron and pancreas homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4979]"}, {"versioned_ensembl_gene_id":"ENSG00000281996.1","gene_symbol":"IGHV3-19","gene_name":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28446","summary":null,"start":106197471,"end":106197761,"strand":-1,"description":"immunoglobulin heavy variable 3-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5584]"}, {"versioned_ensembl_gene_id":"ENSG00000089157.15","gene_symbol":"RPLP0","gene_name":"ribosomal protein lateral stalk subunit P0 [Source:HGNC Symbol;Acc:HGNC:10371]","synonyms":"RPP0,PRLP0,P0,LP0,L10E","biotype":"protein_coding","ncbi_id":"6175","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which is the functional equivalent of the E. coli L10 ribosomal protein, belongs to the L10P family of ribosomal proteins. It is a neutral phosphoprotein with a C-terminal end that is nearly identical to the C-terminal ends of the acidic ribosomal phosphoproteins P1 and P2. The P0 protein can interact with P1 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":120196686,"end":120201235,"strand":-1,"description":"ribosomal protein lateral stalk subunit P0 [Source:HGNC Symbol;Acc:HGNC:10371]"}, {"versioned_ensembl_gene_id":"ENSG00000213648.10","gene_symbol":"SULT1A4","gene_name":"sulfotransferase family 1A member 4 [Source:HGNC Symbol;Acc:HGNC:30004]","synonyms":null,"biotype":"protein_coding","ncbi_id":"445329","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a phenol sulfotransferase with thermolabile enzyme activity. Four sulfotransferase genes are located on the p arm of chromosome 16, this gene and SULT1A3 arose from a segmental duplication. Read-through transcription exists between this gene and the upstream SLX1B (SLX1 structure-specific endonuclease subunit homolog B) gene that encodes a protein containing GIY-YIG domains. [provided by RefSeq, Nov 2010]","start":29459889,"end":29464976,"strand":1,"description":"sulfotransferase family 1A member 4 [Source:HGNC Symbol;Acc:HGNC:30004]"}, {"versioned_ensembl_gene_id":"ENSG00000279228.1","gene_symbol":"AC133555.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29467161,"end":29467578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162714.12","gene_symbol":"ZNF496","gene_name":"zinc finger protein 496 [Source:HGNC Symbol;Acc:HGNC:23713]","synonyms":"ZSCAN49,ZKSCAN17,MGC15548","biotype":"protein_coding","ncbi_id":"84838","summary":null,"start":247297412,"end":247331846,"strand":-1,"description":"zinc finger protein 496 [Source:HGNC Symbol;Acc:HGNC:23713]"}, {"versioned_ensembl_gene_id":"ENSG00000237445.2","gene_symbol":"AL359771.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13657311,"end":13659910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124120.10","gene_symbol":"TTPAL","gene_name":"alpha tocopherol transfer protein like [Source:HGNC Symbol;Acc:HGNC:16114]","synonyms":"dJ179M20.3,C20orf121","biotype":"protein_coding","ncbi_id":"79183","summary":null,"start":44475886,"end":44494603,"strand":1,"description":"alpha tocopherol transfer protein like [Source:HGNC Symbol;Acc:HGNC:16114]"}, {"versioned_ensembl_gene_id":"ENSG00000170748.6","gene_symbol":"RBMXL2","gene_name":"RNA binding motif protein, X-linked like 2 [Source:HGNC Symbol;Acc:HGNC:17886]","synonyms":"HNRPGT,HNRNPG-T","biotype":"protein_coding","ncbi_id":"27288","summary":"This gene belongs to the HNRPG subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two RRM domains that bind RNAs. This gene is intronless and is thought to be derived from a processed retroposon. However, unlike many retroposon-derived genes, this gene is not a pseudogene. The encoded protein has similarity to HNRPG and RBMY proteins and it is suggested to replace HNRPG protein function during meiotic prophase or act as a germ cell-specific splicing regulator. It primarily localizes to the nuclei of meiotic spermatocytes. This gene is a candidate for autosomal male infertility. [provided by RefSeq, Jul 2008]","start":7089027,"end":7090900,"strand":1,"description":"RNA binding motif protein, X-linked like 2 [Source:HGNC Symbol;Acc:HGNC:17886]"}, {"versioned_ensembl_gene_id":"ENSG00000271737.1","gene_symbol":"AC008608.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134005147,"end":134005562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236371.5","gene_symbol":"CT47A1","gene_name":"cancer/testis antigen family 47, member A1 [Source:HGNC Symbol;Acc:HGNC:33282]","synonyms":"CT47.1","biotype":"protein_coding","ncbi_id":"728096","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. This locus is the most telomeric of the cluster.[provided by RefSeq, Sep 2010]","start":120982476,"end":120985788,"strand":-1,"description":"cancer/testis antigen family 47, member A1 [Source:HGNC Symbol;Acc:HGNC:33282]"}, {"versioned_ensembl_gene_id":"ENSG00000282290.1","gene_symbol":"IGHV3-15","gene_name":"immunoglobulin heavy variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5582]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28448","summary":null,"start":106154393,"end":106154934,"strand":-1,"description":"immunoglobulin heavy variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5582]"}, {"versioned_ensembl_gene_id":"ENSG00000258375.2","gene_symbol":"AC079363.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81545326,"end":81546450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228250.2","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"G6c,C6orf24,NG24","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31794930,"end":31798127,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000222043.2","gene_symbol":"AC079305.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177264359,"end":177265515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236649.10","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32220447,"end":32238987,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000256282.1","gene_symbol":"AC112694.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":18595459,"end":18599683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273575.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"103AS,CD158D,15.212","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803379,"end":54814527,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000198089.15","gene_symbol":"SFI1","gene_name":"SFI1 centrin binding protein [Source:HGNC Symbol;Acc:HGNC:29064]","synonyms":"PPP1R139,PISD,KIAA0542","biotype":"protein_coding","ncbi_id":"9814","summary":null,"start":31488688,"end":31618586,"strand":1,"description":"SFI1 centrin binding protein [Source:HGNC Symbol;Acc:HGNC:29064]"}, {"versioned_ensembl_gene_id":"ENSG00000258153.1","gene_symbol":"HSPE1P4","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49323]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287369","summary":null,"start":101873316,"end":101873623,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49323]"}, {"versioned_ensembl_gene_id":"ENSG00000197535.14","gene_symbol":"MYO5A","gene_name":"myosin VA [Source:HGNC Symbol;Acc:HGNC:7602]","synonyms":"GS1,MYR12,MYO5,MYH12","biotype":"protein_coding","ncbi_id":"4644","summary":"This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008]","start":52307283,"end":52529050,"strand":-1,"description":"myosin VA [Source:HGNC Symbol;Acc:HGNC:7602]"}, {"versioned_ensembl_gene_id":"ENSG00000247595.4","gene_symbol":"SPTY2D1-AS1","gene_name":"SPTY2D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44122]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506540","summary":null,"start":18588781,"end":18610255,"strand":1,"description":"SPTY2D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44122]"}, {"versioned_ensembl_gene_id":"ENSG00000253251.2","gene_symbol":"AC008560.1","gene_name":"Uncharacterized protein FLJ26957 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNX1]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":65624765,"end":65630891,"strand":1,"description":"Uncharacterized protein FLJ26957 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZNX1]"}, {"versioned_ensembl_gene_id":"ENSG00000158077.4","gene_symbol":"NLRP14","gene_name":"NLR family pyrin domain containing 14 [Source:HGNC Symbol;Acc:HGNC:22939]","synonyms":"NOD5,NALP14,Nalp-iota,GC-LRR,CLR11.2,PAN8","biotype":"protein_coding","ncbi_id":"338323","summary":"The protein encoded by this gene belongs to the NALP protein family. Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). This protein may play a regulatory role in the innate immune system as similar family members belong to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. [provided by RefSeq, Jul 2008]","start":7020446,"end":7071308,"strand":1,"description":"NLR family pyrin domain containing 14 [Source:HGNC Symbol;Acc:HGNC:22939]"}, {"versioned_ensembl_gene_id":"ENSG00000132671.5","gene_symbol":"SSTR4","gene_name":"somatostatin receptor 4 [Source:HGNC Symbol;Acc:HGNC:11333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6754","summary":"Somatostatin acts at many sites to inhibit the release of many hormones and other secretory proteins. The biologic effects of somatostatin are probably mediated by a family of G protein-coupled receptors that are expressed in a tissue-specific manner. SSTR4 is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in fetal and adult brain and lung. [provided by RefSeq, Jul 2008]","start":23035386,"end":23036812,"strand":1,"description":"somatostatin receptor 4 [Source:HGNC Symbol;Acc:HGNC:11333]"}, {"versioned_ensembl_gene_id":"ENSG00000118960.12","gene_symbol":"HS1BP3","gene_name":"HCLS1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:24979]","synonyms":"HS1-BP3,FLJ14249","biotype":"protein_coding","ncbi_id":"64342","summary":"The protein encoded by this gene shares similarity with mouse Hs1bp3, an Hcls1/Hs1-interacting protein that may be involved in lymphocyte activation. [provided by RefSeq, Jul 2008]","start":20560448,"end":20651089,"strand":-1,"description":"HCLS1 binding protein 3 [Source:HGNC Symbol;Acc:HGNC:24979]"}, {"versioned_ensembl_gene_id":"ENSG00000111196.9","gene_symbol":"MAGOHB","gene_name":"mago homolog B, exon junction complex core component [Source:HGNC Symbol;Acc:HGNC:25504]","synonyms":"MGN2,FLJ10292","biotype":"protein_coding","ncbi_id":"55110","summary":null,"start":10604190,"end":10613623,"strand":-1,"description":"mago homolog B, exon junction complex core component [Source:HGNC Symbol;Acc:HGNC:25504]"}, {"versioned_ensembl_gene_id":"ENSG00000229305.1","gene_symbol":"AL358876.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8189824,"end":8192770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130517.13","gene_symbol":"PGPEP1","gene_name":"pyroglutamyl-peptidase I [Source:HGNC Symbol;Acc:HGNC:13568]","synonyms":"PGPI,PGP-I,PGP,Pcp","biotype":"protein_coding","ncbi_id":"54858","summary":"The gene encodes a cysteine protease and member of the peptidase C15 family of proteins. The encoded protein cleaves amino terminal pyroglutamate residues from protein substrates including thyrotropin-releasing hormone and other neuropeptides. Expression of this gene may be downregulated in colorectal cancer, while activity of the encoded protein may be negatively correlated with cancer progression in colorectal cancer patients. Activity of the encoded protease may also be altered in other disease states including in liver cirrhosis, which is associated with reduced protease activity, and in necrozoospermia, which is associated with elevated protease activity. [provided by RefSeq, Jul 2016]","start":18340587,"end":18369950,"strand":1,"description":"pyroglutamyl-peptidase I [Source:HGNC Symbol;Acc:HGNC:13568]"}, {"versioned_ensembl_gene_id":"ENSG00000269976.1","gene_symbol":"AC012065.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20586248,"end":20586686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174948.5","gene_symbol":"GPR149","gene_name":"G protein-coupled receptor 149 [Source:HGNC Symbol;Acc:HGNC:23627]","synonyms":"PGR10,IEDA","biotype":"protein_coding","ncbi_id":"344758","summary":"This gene encodes a seven-transmembrane G protein coupled receptor (GPCR) class A family member. Although categorized as a class A GPCR, the encoded protein lacks the first two charged amino acids of the highly conserved Asp-Arg-Tyr (DRY) motif found in the third transmembrane helix of class A receptors which is important for efficient G protein-coupled signal transduction. Mice with a knockout of the orthologous gene are viable and have normal maturation of the ovarian follicle, but show enhanced fertility and ovulation. All GPCRs have a common structural architecture consisting of seven transmembrane alpha-helices interconnected by three extracellular and three intracellular loops. A general feature of GPCR signaling is agonist-induced conformational changes in the receptor, leading to activation of the heterotrimeric G proteins, which consist of the guanine nucleotide-binding G-alpha subunit and the dimeric G-beta-gamma subunits. The activated G proteins then bind to and activate numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017]","start":154337672,"end":154429715,"strand":-1,"description":"G protein-coupled receptor 149 [Source:HGNC Symbol;Acc:HGNC:23627]"}, {"versioned_ensembl_gene_id":"ENSG00000240048.1","gene_symbol":"DDX50P2","gene_name":"DEAD-box helicase 50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18975]","synonyms":"RH_II/GuBp2","biotype":"processed_pseudogene","ncbi_id":"100421328","summary":null,"start":154352136,"end":154354799,"strand":-1,"description":"DEAD-box helicase 50 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18975]"}, {"versioned_ensembl_gene_id":"ENSG00000236894.3","gene_symbol":"AL160287.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26577676,"end":26622338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228950.1","gene_symbol":"AC023137.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20451042,"end":20452947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224755.1","gene_symbol":"HMGN1P34","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874447","summary":null,"start":78519593,"end":78520186,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39378]"}, {"versioned_ensembl_gene_id":"ENSG00000266961.1","gene_symbol":"AP005482.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12738965,"end":12750068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168137.15","gene_symbol":"SETD5","gene_name":"SET domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25566]","synonyms":"FLJ10707","biotype":"protein_coding","ncbi_id":"55209","summary":"This function of this gene has yet to be determined but based on sequence similarity to other SET domain proteins it may function as a histone methyltransferase. Mutations in this gene have been associated with an autosomal dominant form of intellectual disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]","start":9397615,"end":9479240,"strand":1,"description":"SET domain containing 5 [Source:HGNC Symbol;Acc:HGNC:25566]"}, {"versioned_ensembl_gene_id":"ENSG00000257890.1","gene_symbol":"AC011595.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106050961,"end":106058254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114796.15","gene_symbol":"KLHL24","gene_name":"kelch like family member 24 [Source:HGNC Symbol;Acc:HGNC:25947]","synonyms":"FLJ20059,DRE1","biotype":"protein_coding","ncbi_id":"54800","summary":"The protein encoded by this gene is a ubiquitin ligase substrate receptor and is regulated by autoubiquitination. Variations in the translation initiation codon of this gene have been found, which result in an N-terminally truncated but more stable protein due to loss of the autoubiquitination function. The more stable mutant protein causes an increased ubiquitin and degradation of keratin 14, which leads to skin fragility and the potentially life-threatening disease epidermolysis bullosa. The encoded protein is also involved in the regulation of kainate receptors. [provided by RefSeq, Mar 2017]","start":183635568,"end":183684477,"strand":1,"description":"kelch like family member 24 [Source:HGNC Symbol;Acc:HGNC:25947]"}, {"versioned_ensembl_gene_id":"ENSG00000274383.1","gene_symbol":"AC103691.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64950916,"end":64951435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257773.1","gene_symbol":"AC011595.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106015897,"end":106017006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188078.5","gene_symbol":"AL022313.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36536656,"end":36537604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273737.3","gene_symbol":"IGLV1-36","gene_name":"immunoglobulin lambda variable 1-36 [Source:HGNC Symbol;Acc:HGNC:5876]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28826","summary":null,"start":22441045,"end":22441552,"strand":1,"description":"immunoglobulin lambda variable 1-36 [Source:HGNC Symbol;Acc:HGNC:5876]"}, {"versioned_ensembl_gene_id":"ENSG00000229038.4","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30475446,"end":30476096,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000216624.3","gene_symbol":"GAPDHP72","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:22955]","synonyms":"GAPDL18,GAPDHL18","biotype":"transcribed_processed_pseudogene","ncbi_id":"346085","summary":null,"start":166058505,"end":166066028,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:22955]"}, {"versioned_ensembl_gene_id":"ENSG00000281471.1","gene_symbol":"IGLV5-37","gene_name":"immunoglobulin lambda variable 5-37 [Source:HGNC Symbol;Acc:HGNC:5922]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28783","summary":null,"start":22436625,"end":22437120,"strand":1,"description":"immunoglobulin lambda variable 5-37 [Source:HGNC Symbol;Acc:HGNC:5922]"}, {"versioned_ensembl_gene_id":"ENSG00000236959.1","gene_symbol":"SULT1D1P","gene_name":"sulfotransferase family 1D member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:30659]","synonyms":"SULT1D1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"133150","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008]","start":69791872,"end":69813888,"strand":-1,"description":"sulfotransferase family 1D member 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:30659]"}, {"versioned_ensembl_gene_id":"ENSG00000140848.16","gene_symbol":"CPNE2","gene_name":"copine 2 [Source:HGNC Symbol;Acc:HGNC:2315]","synonyms":"CPN2","biotype":"protein_coding","ncbi_id":"221184","summary":"Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene is one of several genes that encode a calcium-dependent protein containing two N-terminal type II C2 domains and an integrin A domain-like sequence in the C-terminus. Sequence analysis identified multiple alternatively spliced transcript variants but their full-length natures could not be determined. [provided by RefSeq, Jul 2008]","start":57092537,"end":57148367,"strand":1,"description":"copine 2 [Source:HGNC Symbol;Acc:HGNC:2315]"}, {"versioned_ensembl_gene_id":"ENSG00000267006.1","gene_symbol":"AC008507.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30028741,"end":30029916,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257943.2","gene_symbol":"AC084879.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":95311312,"end":95442482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226410.1","gene_symbol":"AC104058.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":186162949,"end":186163245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224019.1","gene_symbol":"RPL21P32","gene_name":"ribosomal protein L21 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36978]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271161","summary":null,"start":185956587,"end":185957063,"strand":-1,"description":"ribosomal protein L21 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36978]"}, {"versioned_ensembl_gene_id":"ENSG00000071626.16","gene_symbol":"DAZAP1","gene_name":"DAZ associated protein 1 [Source:HGNC Symbol;Acc:HGNC:2683]","synonyms":"MGC19907","biotype":"protein_coding","ncbi_id":"26528","summary":"In mammals, the Y chromosome directs the development of the testes and plays an important role in spermatogenesis. A high percentage of infertile men have deletions that map to regions of the Y chromosome. The DAZ (deleted in azoospermia) gene cluster maps to the AZFc region of the Y chromosome and is deleted in many azoospermic and severely oligospermic men. It is thought that the DAZ gene cluster arose from the transposition, amplification, and pruning of the ancestral autosomal gene DAZL also involved in germ cell development and gametogenesis. This gene encodes a RNA-binding protein with two RNP motifs that was originally identified by its interaction with the infertility factors DAZ and DAZL. Two isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]","start":1407569,"end":1435687,"strand":1,"description":"DAZ associated protein 1 [Source:HGNC Symbol;Acc:HGNC:2683]"}, {"versioned_ensembl_gene_id":"ENSG00000167077.12","gene_symbol":"MEI1","gene_name":"meiotic double-stranded break formation protein 1 [Source:HGNC Symbol;Acc:HGNC:28613]","synonyms":"SPATA38,MGC40042","biotype":"protein_coding","ncbi_id":"150365","summary":null,"start":41699499,"end":41799456,"strand":1,"description":"meiotic double-stranded break formation protein 1 [Source:HGNC Symbol;Acc:HGNC:28613]"}, {"versioned_ensembl_gene_id":"ENSG00000256746.5","gene_symbol":"AC018410.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47270657,"end":47272110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282644.1","gene_symbol":"AC247036.5","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106088893,"end":106089344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274839.5","gene_symbol":"PRB4","gene_name":"proline rich protein BstNI subfamily 4 [Source:HGNC Symbol;Acc:HGNC:9340]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5545","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Small\" allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015]","start":11303340,"end":11306692,"strand":-1,"description":"proline rich protein BstNI subfamily 4 [Source:HGNC Symbol;Acc:HGNC:9340]"}, {"versioned_ensembl_gene_id":"ENSG00000127362.2","gene_symbol":"TAS2R3","gene_name":"taste 2 receptor member 3 [Source:HGNC Symbol;Acc:HGNC:14910]","synonyms":"T2R3","biotype":"protein_coding","ncbi_id":"50831","summary":"This gene encodes a member of a family of candidate taste receptors that are members of the G protein-coupled receptor superfamily and that are specifically expressed by taste receptor cells of the tongue and palate epithelia. These apparently intronless taste receptor genes encode a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered with another 3 candidate taste receptor genes in chromosome 7 and is genetically linked to loci that influence bitter perception. [provided by RefSeq, Jul 2008]","start":141764097,"end":141765197,"strand":1,"description":"taste 2 receptor member 3 [Source:HGNC Symbol;Acc:HGNC:14910]"}, {"versioned_ensembl_gene_id":"ENSG00000270923.1","gene_symbol":"TAS2R6P","gene_name":"taste 2 receptor member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:20616]","synonyms":"TAS2R6,T2R6,T2R06","biotype":"processed_pseudogene","ncbi_id":"448990","summary":null,"start":141787815,"end":141788640,"strand":1,"description":"taste 2 receptor member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:20616]"}, {"versioned_ensembl_gene_id":"ENSG00000129003.15","gene_symbol":"VPS13C","gene_name":"vacuolar protein sorting 13 homolog C [Source:HGNC Symbol;Acc:HGNC:23594]","synonyms":"KIAA1421,FLJ20136,FLJ10381","biotype":"protein_coding","ncbi_id":"54832","summary":"This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]","start":61852389,"end":62060473,"strand":-1,"description":"vacuolar protein sorting 13 homolog C [Source:HGNC Symbol;Acc:HGNC:23594]"}, {"versioned_ensembl_gene_id":"ENSG00000261617.1","gene_symbol":"LINC02177","gene_name":"long intergenic non-protein coding RNA 2177 [Source:HGNC Symbol;Acc:HGNC:53039]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927009","summary":null,"start":9355588,"end":9408093,"strand":1,"description":"long intergenic non-protein coding RNA 2177 [Source:HGNC Symbol;Acc:HGNC:53039]"}, {"versioned_ensembl_gene_id":"ENSG00000203650.8","gene_symbol":"LINC01285","gene_name":"long intergenic non-protein coding RNA 1285 [Source:HGNC Symbol;Acc:HGNC:50344]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928287","summary":null,"start":118839554,"end":118919669,"strand":1,"description":"long intergenic non-protein coding RNA 1285 [Source:HGNC Symbol;Acc:HGNC:50344]"}, {"versioned_ensembl_gene_id":"ENSG00000274251.1","gene_symbol":"AP003419.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67353629,"end":67354348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155893.12","gene_symbol":"PXYLP1","gene_name":"2-phosphoxylose phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:26303]","synonyms":"FLJ23751,ACPL2","biotype":"protein_coding","ncbi_id":"92370","summary":null,"start":141228726,"end":141367753,"strand":1,"description":"2-phosphoxylose phosphatase 1 [Source:HGNC Symbol;Acc:HGNC:26303]"}, {"versioned_ensembl_gene_id":"ENSG00000181524.6","gene_symbol":"RPL24P4","gene_name":"ribosomal protein L24 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21371]","synonyms":"dJ125M3.1","biotype":"processed_pseudogene","ncbi_id":"377381","summary":null,"start":42956345,"end":42956765,"strand":-1,"description":"ribosomal protein L24 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21371]"}, {"versioned_ensembl_gene_id":"ENSG00000260303.1","gene_symbol":"AC108206.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146052604,"end":146056762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231113.2","gene_symbol":"AL035587.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42940364,"end":42948360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073060.15","gene_symbol":"SCARB1","gene_name":"scavenger receptor class B member 1 [Source:HGNC Symbol;Acc:HGNC:1664]","synonyms":"SRB1,SR-BI,CLA1,CLA-1,CD36L1","biotype":"protein_coding","ncbi_id":"949","summary":"The protein encoded by this gene is a plasma membrane receptor for high density lipoprotein cholesterol (HDL). The encoded protein mediates cholesterol transfer to and from HDL. In addition, this protein is a receptor for hepatitis C virus glycoprotein E2. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2019]","start":124776856,"end":124882668,"strand":-1,"description":"scavenger receptor class B member 1 [Source:HGNC Symbol;Acc:HGNC:1664]"}, {"versioned_ensembl_gene_id":"ENSG00000227974.1","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"unprocessed_pseudogene","ncbi_id":"285834","summary":null,"start":31046946,"end":31052246,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000261136.1","gene_symbol":"AC023908.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39782571,"end":39785617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227584.2","gene_symbol":"MTND4P5","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42192]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873191","summary":null,"start":57192695,"end":57194068,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42192]"}, {"versioned_ensembl_gene_id":"ENSG00000224448.1","gene_symbol":"AC005020.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99638242,"end":99638767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242575.1","gene_symbol":"AC012501.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":153420677,"end":153421957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139726.10","gene_symbol":"DENR","gene_name":"density regulated re-initiation and release factor [Source:HGNC Symbol;Acc:HGNC:2769]","synonyms":"SMAP-3,DRP1,DRP","biotype":"protein_coding","ncbi_id":"8562","summary":"This gene encodes a protein whose expression was found to increase in cultured cells at high density but not during growth arrest. This gene was also shown to have increased expression in cells overexpressing HER-2/neu proto-oncogene. The protein contains an SUI1 domain. In budding yeast, SUI1 is a translation initiation factor that along with eIF-2 and the initiator tRNA-Met, directs the ribosome to the proper translation start site. Proteins similar to SUI have been found in mammals, insects, and plants. [provided by RefSeq, Jul 2008]","start":122752774,"end":122771064,"strand":1,"description":"density regulated re-initiation and release factor [Source:HGNC Symbol;Acc:HGNC:2769]"}, {"versioned_ensembl_gene_id":"ENSG00000272155.1","gene_symbol":"AC055822.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65714334,"end":65714778,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265788.2","gene_symbol":"AC015688.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27651334,"end":27665712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259208.2","gene_symbol":"AC023968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79668342,"end":79668816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236463.1","gene_symbol":"LINC00427","gene_name":"long intergenic non-protein coding RNA 427 [Source:HGNC Symbol;Acc:HGNC:42762]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507040","summary":null,"start":30316360,"end":30319903,"strand":-1,"description":"long intergenic non-protein coding RNA 427 [Source:HGNC Symbol;Acc:HGNC:42762]"}, {"versioned_ensembl_gene_id":"ENSG00000118777.10","gene_symbol":"ABCG2","gene_name":"ATP binding cassette subfamily G member 2 (Junior blood group) [Source:HGNC Symbol;Acc:HGNC:74]","synonyms":"MXR,EST157481,CD338,BCRP,ABCP","biotype":"protein_coding","ncbi_id":"9429","summary":"The membrane-associated protein encoded by this gene is included in the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. Alternatively referred to as a breast cancer resistance protein, this protein functions as a xenobiotic transporter which may play a major role in multi-drug resistance. It likely serves as a cellular defense mechanism in response to mitoxantrone and anthracycline exposure. Significant expression of this protein has been observed in the placenta, which may suggest a potential role for this molecule in placenta tissue. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":88090264,"end":88231322,"strand":-1,"description":"ATP binding cassette subfamily G member 2 (Junior blood group) [Source:HGNC Symbol;Acc:HGNC:74]"}, {"versioned_ensembl_gene_id":"ENSG00000231981.3","gene_symbol":"RPL7L1P12","gene_name":"ribosomal protein L7 like 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39811]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420200","summary":null,"start":98949719,"end":98950447,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39811]"}, {"versioned_ensembl_gene_id":"ENSG00000174460.3","gene_symbol":"ZCCHC12","gene_name":"zinc finger CCHC-type containing 12 [Source:HGNC Symbol;Acc:HGNC:27273]","synonyms":"SIZN1,SIZN,PNMA7A,FLJ16123","biotype":"protein_coding","ncbi_id":"170261","summary":"This gene encodes a downstream effector of bone morphogenetic protein (BMP) signalling. This protein contains a zinc finger domain and functions as a transcriptional coactivator. Variation in this gene may be associated with X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":118823790,"end":118826968,"strand":1,"description":"zinc finger CCHC-type containing 12 [Source:HGNC Symbol;Acc:HGNC:27273]"}, {"versioned_ensembl_gene_id":"ENSG00000282223.1","gene_symbol":"IGHV4-4","gene_name":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28401","summary":null,"start":106012693,"end":106013191,"strand":-1,"description":"immunoglobulin heavy variable 4-4 [Source:HGNC Symbol;Acc:HGNC:5652]"}, {"versioned_ensembl_gene_id":"ENSG00000275326.4","gene_symbol":"NOSTRIN","gene_name":"nitric oxide synthase trafficking [Source:HGNC Symbol;Acc:HGNC:20203]","synonyms":"MGC20702","biotype":"protein_coding","ncbi_id":"115677","summary":"Nitric oxide (NO) is a potent mediator in biologic processes such as neurotransmission, inflammatory response, and vascular homeostasis. NOSTRIN binds the enzyme responsible for NO production, endothelial NO synthase (ENOS; MIM 163729), and triggers the translocation of ENOS from the plasma membrane to vesicle-like subcellular structures, thereby attenuating ENOS-dependent NO production.[supplied by OMIM, Apr 2004]","start":168831472,"end":168865516,"strand":1,"description":"nitric oxide synthase trafficking [Source:HGNC Symbol;Acc:HGNC:20203]"}, {"versioned_ensembl_gene_id":"ENSG00000253223.1","gene_symbol":"AC110998.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66984135,"end":66986187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206168.1","gene_symbol":"Z69890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231134,"end":231472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131174.4","gene_symbol":"COX7B","gene_name":"cytochrome c oxidase subunit 7B [Source:HGNC Symbol;Acc:HGNC:2291]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1349","summary":"Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes subunit VIIb, which is highly similar to bovine COX VIIb protein and is found in all tissues. This gene may have several pseudogenes on chromosomes 1, 2, 20 and 22. [provided by RefSeq, Jun 2011]","start":77899438,"end":77907373,"strand":1,"description":"cytochrome c oxidase subunit 7B [Source:HGNC Symbol;Acc:HGNC:2291]"}, {"versioned_ensembl_gene_id":"ENSG00000248206.1","gene_symbol":"AC074194.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":183987678,"end":183988750,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136560.13","gene_symbol":"TANK","gene_name":"TRAF family member associated NFKB activator [Source:HGNC Symbol;Acc:HGNC:11562]","synonyms":"TRAF2,I-TRAF","biotype":"protein_coding","ncbi_id":"10010","summary":"The TRAF (tumor necrosis factor receptor-associated factor) family of proteins associate with and transduce signals from members of the tumor necrosis factor receptor superfamily. The protein encoded by this gene is found in the cytoplasm and can bind to TRAF1, TRAF2, or TRAF3, thereby inhibiting TRAF function by sequestering the TRAFs in a latent state in the cytoplasm. For example, the protein encoded by this gene can block TRAF2 binding to LMP1, the Epstein-Barr virus transforming protein, and inhibit LMP1-mediated NF-kappa-B activation. Three alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":161136908,"end":161236221,"strand":1,"description":"TRAF family member associated NFKB activator [Source:HGNC Symbol;Acc:HGNC:11562]"}, {"versioned_ensembl_gene_id":"ENSG00000077147.14","gene_symbol":"TM9SF3","gene_name":"transmembrane 9 superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:21529]","synonyms":"SMBP","biotype":"protein_coding","ncbi_id":"56889","summary":null,"start":96518109,"end":96587452,"strand":-1,"description":"transmembrane 9 superfamily member 3 [Source:HGNC Symbol;Acc:HGNC:21529]"}, {"versioned_ensembl_gene_id":"ENSG00000178184.15","gene_symbol":"PARD6G","gene_name":"par-6 family cell polarity regulator gamma [Source:HGNC Symbol;Acc:HGNC:16076]","synonyms":"PAR6gamma,PAR-6G","biotype":"protein_coding","ncbi_id":"84552","summary":null,"start":80157232,"end":80247546,"strand":-1,"description":"par-6 family cell polarity regulator gamma [Source:HGNC Symbol;Acc:HGNC:16076]"}, {"versioned_ensembl_gene_id":"ENSG00000160808.9","gene_symbol":"MYL3","gene_name":"myosin light chain 3 [Source:HGNC Symbol;Acc:HGNC:7584]","synonyms":"VLC1,MLC1V,MLC1SB,CMH8","biotype":"protein_coding","ncbi_id":"4634","summary":"MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]","start":46857872,"end":46882169,"strand":-1,"description":"myosin light chain 3 [Source:HGNC Symbol;Acc:HGNC:7584]"}, {"versioned_ensembl_gene_id":"ENSG00000280439.1","gene_symbol":"AC004836.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":106035798,"end":106036431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282057.1","gene_symbol":"AC092807.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85482281,"end":85578250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175087.9","gene_symbol":"PDIK1L","gene_name":"PDLIM1 interacting kinase 1 like [Source:HGNC Symbol;Acc:HGNC:18981]","synonyms":"CLIK1L","biotype":"protein_coding","ncbi_id":"149420","summary":null,"start":26111165,"end":26125543,"strand":1,"description":"PDLIM1 interacting kinase 1 like [Source:HGNC Symbol;Acc:HGNC:18981]"}, {"versioned_ensembl_gene_id":"ENSG00000273264.1","gene_symbol":"AL360219.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85467295,"end":85467660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215086.2","gene_symbol":"NPM1P24","gene_name":"nucleophosmin 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:45097]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422312","summary":null,"start":72917641,"end":72918534,"strand":-1,"description":"nucleophosmin 1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:45097]"}, {"versioned_ensembl_gene_id":"ENSG00000269383.2","gene_symbol":"AC012493.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100370255,"end":100370545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281940.1","gene_symbol":"IGHD4-11","gene_name":"immunoglobulin heavy diversity 4-11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5502]","synonyms":"IGHD411,DA1","biotype":"IG_D_gene","ncbi_id":"28495","summary":null,"start":105904387,"end":105904402,"strand":-1,"description":"immunoglobulin heavy diversity 4-11 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5502]"}, {"versioned_ensembl_gene_id":"ENSG00000236720.1","gene_symbol":"LINC01741","gene_name":"long intergenic non-protein coding RNA 1741 [Source:HGNC Symbol;Acc:HGNC:52529]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928778","summary":null,"start":177700524,"end":177710330,"strand":1,"description":"long intergenic non-protein coding RNA 1741 [Source:HGNC Symbol;Acc:HGNC:52529]"}, {"versioned_ensembl_gene_id":"ENSG00000248577.1","gene_symbol":"AC091435.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38763158,"end":38764289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232084.5","gene_symbol":"LINC01104","gene_name":"long intergenic non-protein coding RNA 1104 [Source:HGNC Symbol;Acc:HGNC:49226]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150577","summary":null,"start":100208254,"end":100251484,"strand":1,"description":"long intergenic non-protein coding RNA 1104 [Source:HGNC Symbol;Acc:HGNC:49226]"}, {"versioned_ensembl_gene_id":"ENSG00000226624.1","gene_symbol":"AC005099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105819492,"end":105820101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131067.16","gene_symbol":"GGT7","gene_name":"gamma-glutamyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4259]","synonyms":"GGTL5,GGTL3,dJ18C9.2,D20S101","biotype":"protein_coding","ncbi_id":"2686","summary":"This gene is a member of a gene family that encodes enzymes involved in both the metabolism of glutathione and in the transpeptidation of amino acids. Changes in the activity of gamma-glutamyltransferase may signal preneoplastic or toxic conditions in the liver or kidney. The protein encoded by this gene consists of a heavy and a light chain, and it can interact with CT120, a plasma membrane-associated protein that is possibly involved in lung carcinogenesis. [provided by RefSeq, Jul 2008]","start":34844720,"end":34872860,"strand":-1,"description":"gamma-glutamyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:4259]"}, {"versioned_ensembl_gene_id":"ENSG00000263324.5","gene_symbol":"HCN3","gene_name":"hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Source:HGNC Symbol;Acc:HGNC:19183]","synonyms":"KIAA1535","biotype":"protein_coding","ncbi_id":"57657","summary":"This gene encodes a multi-pass membrane protein that functions as a voltage gated cation channel. The encoded protein is a member of a family of closely related cyclic adenosine monophosphate-binding channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":155292987,"end":155305252,"strand":1,"description":"hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Source:HGNC Symbol;Acc:HGNC:19183]"}, {"versioned_ensembl_gene_id":"ENSG00000237500.1","gene_symbol":"AL713851.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2499721,"end":2500570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263400.6","gene_symbol":"TMEM220-AS1","gene_name":"TMEM220 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44357]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101101775","summary":null,"start":10729777,"end":10815164,"strand":1,"description":"TMEM220 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44357]"}, {"versioned_ensembl_gene_id":"ENSG00000078114.18","gene_symbol":"NEBL","gene_name":"nebulette [Source:HGNC Symbol;Acc:HGNC:16932]","synonyms":"LNEBL,LASP2","biotype":"protein_coding","ncbi_id":"10529","summary":"This gene encodes a nebulin like protein that is abundantly expressed in cardiac muscle. The encoded protein binds actin and interacts with thin filaments and Z-line associated proteins in striated muscle. This protein may be involved in cardiac myofibril assembly. A shorter isoform of this protein termed LIM nebulette is expressed in non-muscle cells and may function as a component of focal adhesion complexes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":20779973,"end":21174187,"strand":-1,"description":"nebulette [Source:HGNC Symbol;Acc:HGNC:16932]"}, {"versioned_ensembl_gene_id":"ENSG00000238107.1","gene_symbol":"AC245100.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148295180,"end":148297556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177731.15","gene_symbol":"FLII","gene_name":"FLII, actin remodeling protein [Source:HGNC Symbol;Acc:HGNC:3750]","synonyms":"MGC39265,FLIL,Fli1,FLI","biotype":"protein_coding","ncbi_id":"2314","summary":"This gene encodes a protein with a gelsolin-like actin binding domain and an N-terminal leucine-rich repeat-protein protein interaction domain. The protein is similar to a Drosophila protein involved in early embryogenesis and the structural organization of indirect flight muscle. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":18244836,"end":18258916,"strand":-1,"description":"FLII, actin remodeling protein [Source:HGNC Symbol;Acc:HGNC:3750]"}, {"versioned_ensembl_gene_id":"ENSG00000251368.1","gene_symbol":"AC016632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55750206,"end":55750401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234129.7","gene_symbol":"AC073529.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10847877,"end":11111141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177352.9","gene_symbol":"CCDC71","gene_name":"coiled-coil domain containing 71 [Source:HGNC Symbol;Acc:HGNC:25760]","synonyms":"FLJ12800","biotype":"protein_coding","ncbi_id":"64925","summary":null,"start":49162535,"end":49166321,"strand":-1,"description":"coiled-coil domain containing 71 [Source:HGNC Symbol;Acc:HGNC:25760]"}, {"versioned_ensembl_gene_id":"ENSG00000280971.1","gene_symbol":"AC236592.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177967004,"end":177967457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243897.8","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"C6orf8,NG3","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32203996,"end":32207669,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000064835.10","gene_symbol":"POU1F1","gene_name":"POU class 1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9210]","synonyms":"POU1F1a,PIT1,GHF-1","biotype":"protein_coding","ncbi_id":"5449","summary":"This gene encodes a member of the POU family of transcription factors that regulate mammalian development. The protein regulates expression of several genes involved in pituitary development and hormone expression. Mutations in this genes result in combined pituitary hormone deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":87259404,"end":87276587,"strand":-1,"description":"POU class 1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9210]"}, {"versioned_ensembl_gene_id":"ENSG00000281498.1","gene_symbol":"AL132642.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93939555,"end":93944129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225228.2","gene_symbol":"MCCD1","gene_name":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401250","summary":null,"start":31595673,"end":31597188,"strand":1,"description":"mitochondrial coiled-coil domain 1 [Source:HGNC Symbol;Acc:HGNC:20668]"}, {"versioned_ensembl_gene_id":"ENSG00000128654.13","gene_symbol":"MTX2","gene_name":"metaxin 2 [Source:HGNC Symbol;Acc:HGNC:7506]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10651","summary":"The protein encoded by this gene is highly similar to the metaxin 2 protein from mouse, which has been shown to interact with the mitochondrial membrane protein metaxin 1. Because of this similarity, it is thought that the encoded protein is peripherally associated with the cytosolic face of the outer mitochondrial membrane, and that it is involved in the import of proteins into the mitochondrion. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Jun 2009]","start":176269395,"end":176338025,"strand":1,"description":"metaxin 2 [Source:HGNC Symbol;Acc:HGNC:7506]"}, {"versioned_ensembl_gene_id":"ENSG00000278343.1","gene_symbol":"AL356130.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":958324,"end":962272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269915.1","gene_symbol":"AP006621.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":708564,"end":727047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235748.1","gene_symbol":"SEPT14P12","gene_name":"septin 14 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480343","summary":null,"start":197138748,"end":197139307,"strand":-1,"description":"septin 14 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51699]"}, {"versioned_ensembl_gene_id":"ENSG00000228440.1","gene_symbol":"MTND5P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42268]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873196","summary":null,"start":57170974,"end":57172771,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42268]"}, {"versioned_ensembl_gene_id":"ENSG00000230243.1","gene_symbol":"FKBP1AP3","gene_name":"FK506 binding protein 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3716]","synonyms":"FKBP1P3","biotype":"processed_pseudogene","ncbi_id":"2284","summary":null,"start":46505118,"end":46505436,"strand":1,"description":"FK506 binding protein 1A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3716]"}, {"versioned_ensembl_gene_id":"ENSG00000277228.1","gene_symbol":"AL138686.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46474246,"end":46493268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205105.6","gene_symbol":"COX17P1","gene_name":"COX17, cytochrome c oxidase copper chaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24341]","synonyms":"COX17P","biotype":"processed_pseudogene","ncbi_id":"81993","summary":null,"start":46490930,"end":46491121,"strand":1,"description":"COX17, cytochrome c oxidase copper chaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24341]"}, {"versioned_ensembl_gene_id":"ENSG00000227799.1","gene_symbol":"AC012358.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55224280,"end":55225908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267225.1","gene_symbol":"WDR7-OT1","gene_name":"WDR7 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:45131]","synonyms":"WDR7-UT1,WDR7-UA1","biotype":"sense_overlapping","ncbi_id":"107985140","summary":null,"start":57027832,"end":57038845,"strand":1,"description":"WDR7 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:45131]"}, {"versioned_ensembl_gene_id":"ENSG00000276469.1","gene_symbol":"GPR179","gene_name":"G protein-coupled receptor 179 [Source:HGNC Symbol;Acc:HGNC:31371]","synonyms":"GPR158L1,CSNB1E","biotype":"protein_coding","ncbi_id":"440435","summary":"This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]","start":38126026,"end":38144226,"strand":-1,"description":"G protein-coupled receptor 179 [Source:HGNC Symbol;Acc:HGNC:31371]"}, {"versioned_ensembl_gene_id":"ENSG00000140374.15","gene_symbol":"ETFA","gene_name":"electron transfer flavoprotein alpha subunit [Source:HGNC Symbol;Acc:HGNC:3481]","synonyms":"MADD,GA2,EMA","biotype":"protein_coding","ncbi_id":"2108","summary":"ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":76215355,"end":76311472,"strand":-1,"description":"electron transfer flavoprotein alpha subunit [Source:HGNC Symbol;Acc:HGNC:3481]"}, {"versioned_ensembl_gene_id":"ENSG00000170471.14","gene_symbol":"RALGAPB","gene_name":"Ral GTPase activating protein non-catalytic beta subunit [Source:HGNC Symbol;Acc:HGNC:29221]","synonyms":"RalGAPbeta,KIAA1219,DKFZp781M2411","biotype":"protein_coding","ncbi_id":"57148","summary":null,"start":38472816,"end":38578861,"strand":1,"description":"Ral GTPase activating protein non-catalytic beta subunit [Source:HGNC Symbol;Acc:HGNC:29221]"}, {"versioned_ensembl_gene_id":"ENSG00000121671.11","gene_symbol":"CRY2","gene_name":"cryptochrome circadian clock 2 [Source:HGNC Symbol;Acc:HGNC:2385]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1408","summary":"This gene encodes a flavin adenine dinucleotide-binding protein that is a key component of the circadian core oscillator complex, which regulates the circadian clock. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene have been associated with altered sleep patterns. The encoded protein is widely conserved across plants and animals. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]","start":45847118,"end":45883248,"strand":1,"description":"cryptochrome circadian clock 2 [Source:HGNC Symbol;Acc:HGNC:2385]"}, {"versioned_ensembl_gene_id":"ENSG00000225502.2","gene_symbol":"GAPDHP16","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:23768]","synonyms":"GAPDP16","biotype":"processed_pseudogene","ncbi_id":"387491","summary":null,"start":14774301,"end":14775262,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:23768]"}, {"versioned_ensembl_gene_id":"ENSG00000154957.13","gene_symbol":"ZNF18","gene_name":"zinc finger protein 18 [Source:HGNC Symbol;Acc:HGNC:12969]","synonyms":"ZSCAN38,ZNF535,ZKSCAN6,Zfp535,KOX11,HDSG1","biotype":"protein_coding","ncbi_id":"7566","summary":null,"start":11977439,"end":11997510,"strand":-1,"description":"zinc finger protein 18 [Source:HGNC Symbol;Acc:HGNC:12969]"}, {"versioned_ensembl_gene_id":"ENSG00000134531.9","gene_symbol":"EMP1","gene_name":"epithelial membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:3333]","synonyms":"TMP,CL-20","biotype":"protein_coding","ncbi_id":"2012","summary":null,"start":13196716,"end":13219939,"strand":1,"description":"epithelial membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:3333]"}, {"versioned_ensembl_gene_id":"ENSG00000204388.6","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31827735,"end":31830255,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000226751.2","gene_symbol":"AF127936.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14761710,"end":14763090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232423.6","gene_symbol":"PRAMEF6","gene_name":"PRAME family member 6 [Source:HGNC Symbol;Acc:HGNC:30583]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440561","summary":null,"start":12938472,"end":12947580,"strand":-1,"description":"PRAME family member 6 [Source:HGNC Symbol;Acc:HGNC:30583]"}, {"versioned_ensembl_gene_id":"ENSG00000204390.9","gene_symbol":"HSPA1L","gene_name":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]","synonyms":"hum70t,HSP70-HOM","biotype":"protein_coding","ncbi_id":"3305","summary":"This gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein. [provided by RefSeq, Jul 2008]","start":31809619,"end":31815065,"strand":-1,"description":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]"}, {"versioned_ensembl_gene_id":"ENSG00000232156.1","gene_symbol":"AL662842.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32483164,"end":32497705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232576.2","gene_symbol":"AL645638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88908403,"end":88908763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228971.2","gene_symbol":"AL356479.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95510116,"end":95782342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204179.10","gene_symbol":"PTPN20","gene_name":"protein tyrosine phosphatase, non-receptor type 20 [Source:HGNC Symbol;Acc:HGNC:23423]","synonyms":"PTPN20B,PTPN20A,DKFZP566K0524,CT126,bA42B19.1,bA142I17.1","biotype":"protein_coding","ncbi_id":"26095","summary":"The product of this gene belongs to the family of classical tyrosine-specific protein tyrosine phosphatases. Many protein tyrosine phosphatases have been shown to regulate fundamental cellular processes. The encoded protein appears to be targeted to sites of actin polymerization. A pseudogene of this gene has been defined on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":46911396,"end":47002488,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 20 [Source:HGNC Symbol;Acc:HGNC:23423]"}, {"versioned_ensembl_gene_id":"ENSG00000171587.14","gene_symbol":"DSCAM","gene_name":"DS cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:3039]","synonyms":"CHD2-52,CHD2-42","biotype":"protein_coding","ncbi_id":"1826","summary":"This gene is a member of the immunoglobulin superfamily of cell adhesion molecules (Ig-CAMs), and is involved in human central and peripheral nervous system development. This gene is a candidate for Down syndrome and congenital heart disease (DSCHD). A gene encoding a similar Ig-CAM protein is located on chromosome 11. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":40010999,"end":40847139,"strand":-1,"description":"DS cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:3039]"}, {"versioned_ensembl_gene_id":"ENSG00000197430.10","gene_symbol":"OPALIN","gene_name":"oligodendrocytic myelin paranodal and inner loop protein [Source:HGNC Symbol;Acc:HGNC:20707]","synonyms":"TMP10,TMEM10,HTMP10","biotype":"protein_coding","ncbi_id":"93377","summary":null,"start":96343216,"end":96359365,"strand":-1,"description":"oligodendrocytic myelin paranodal and inner loop protein [Source:HGNC Symbol;Acc:HGNC:20707]"}, {"versioned_ensembl_gene_id":"ENSG00000259248.5","gene_symbol":"USP3-AS1","gene_name":"USP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44140]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100130855","summary":null,"start":63544247,"end":63601589,"strand":-1,"description":"USP3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44140]"}, {"versioned_ensembl_gene_id":"ENSG00000165675.16","gene_symbol":"ENOX2","gene_name":"ecto-NOX disulfide-thiol exchanger 2 [Source:HGNC Symbol;Acc:HGNC:2259]","synonyms":"tNOX,COVA1,APK1","biotype":"protein_coding","ncbi_id":"10495","summary":"This gene is a tumor-specific member of the ECTO-NOX family of genes that encode cell surface NADH oxidases. The encoded protein has two enzymatic activities: catalysis of hydroquinone or NADH oxidation, and protein disulfide interchange. The protein also displays prion-like properties. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":130623369,"end":130903317,"strand":-1,"description":"ecto-NOX disulfide-thiol exchanger 2 [Source:HGNC Symbol;Acc:HGNC:2259]"}, {"versioned_ensembl_gene_id":"ENSG00000236160.1","gene_symbol":"AC005345.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26657291,"end":26657507,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069509.5","gene_symbol":"FUNDC1","gene_name":"FUN14 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28746]","synonyms":"MGC51029","biotype":"protein_coding","ncbi_id":"139341","summary":"This gene encodes a protein with a FUN14 superfamily domain. The function of the encoded protein is not known. [provided by RefSeq, Sep 2011]","start":44523639,"end":44543001,"strand":-1,"description":"FUN14 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28746]"}, {"versioned_ensembl_gene_id":"ENSG00000273641.2","gene_symbol":"DEFB103B","gene_name":"defensin beta 103B [Source:HGNC Symbol;Acc:HGNC:31702]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55894","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 103, which has broad spectrum antimicrobial activity and may play an important role in innate epithelial defense. [provided by RefSeq, Oct 2014]","start":7420832,"end":7422292,"strand":-1,"description":"defensin beta 103B [Source:HGNC Symbol;Acc:HGNC:31702]"}, {"versioned_ensembl_gene_id":"ENSG00000175746.6","gene_symbol":"C15orf54","gene_name":"chromosome 15 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:33797]","synonyms":"FLJ39531","biotype":"lincRNA","ncbi_id":"400360","summary":null,"start":39250684,"end":39254845,"strand":1,"description":"chromosome 15 open reading frame 54 [Source:HGNC Symbol;Acc:HGNC:33797]"}, {"versioned_ensembl_gene_id":"ENSG00000275444.2","gene_symbol":"DEFB4B","gene_name":"defensin beta 4B [Source:HGNC Symbol;Acc:HGNC:30193]","synonyms":"DEFB4P","biotype":"protein_coding","ncbi_id":"100289462","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 4, an antibiotic peptide which is locally regulated by inflammation. [provided by RefSeq, Oct 2014]","start":7406786,"end":7408809,"strand":-1,"description":"defensin beta 4B [Source:HGNC Symbol;Acc:HGNC:30193]"}, {"versioned_ensembl_gene_id":"ENSG00000272175.1","gene_symbol":"AL050343.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51801028,"end":51801307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117593.9","gene_symbol":"DARS2","gene_name":"aspartyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25538]","synonyms":"FLJ10514","biotype":"protein_coding","ncbi_id":"55157","summary":"The protein encoded by this gene belongs to the class-II aminoacyl-tRNA synthetase family. It is a mitochondrial enzyme that specifically aminoacylates aspartyl-tRNA. Mutations in this gene are associated with leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL). [provided by RefSeq, Nov 2009]","start":173824503,"end":173858546,"strand":1,"description":"aspartyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25538]"}, {"versioned_ensembl_gene_id":"ENSG00000230434.1","gene_symbol":"LINC01650","gene_name":"long intergenic non-protein coding RNA 1650 [Source:HGNC Symbol;Acc:HGNC:52437]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928169","summary":null,"start":95351251,"end":95352254,"strand":-1,"description":"long intergenic non-protein coding RNA 1650 [Source:HGNC Symbol;Acc:HGNC:52437]"}, {"versioned_ensembl_gene_id":"ENSG00000120594.16","gene_symbol":"PLXDC2","gene_name":"plexin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21013]","synonyms":"TEM7R,FLJ14623","biotype":"protein_coding","ncbi_id":"84898","summary":null,"start":19816239,"end":20289856,"strand":1,"description":"plexin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21013]"}, {"versioned_ensembl_gene_id":"ENSG00000227742.2","gene_symbol":"CALR4P","gene_name":"calreticulin 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:35456]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"441884","summary":null,"start":51561866,"end":51594897,"strand":-1,"description":"calreticulin 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:35456]"}, {"versioned_ensembl_gene_id":"ENSG00000224033.1","gene_symbol":"CDY8P","gene_name":"chromodomain Y-linked 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:23855]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386732","summary":null,"start":18022299,"end":18023908,"strand":1,"description":"chromodomain Y-linked 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:23855]"}, {"versioned_ensembl_gene_id":"ENSG00000177917.10","gene_symbol":"ARL6IP6","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 6 [Source:HGNC Symbol;Acc:HGNC:24048]","synonyms":"MGC33864","biotype":"protein_coding","ncbi_id":"151188","summary":null,"start":152717893,"end":152761253,"strand":1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 6 [Source:HGNC Symbol;Acc:HGNC:24048]"}, {"versioned_ensembl_gene_id":"ENSG00000075711.20","gene_symbol":"DLG1","gene_name":"discs large MAGUK scaffold protein 1 [Source:HGNC Symbol;Acc:HGNC:2900]","synonyms":"SAP97,SAP-97,hdlg,DLGH1,dJ1061C18.1.1","biotype":"protein_coding","ncbi_id":"1739","summary":"This gene encodes a multi-domain scaffolding protein that is required for normal development. This protein may have a role in septate junction formation, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. A multitude of transcript variants deriving from alternative splicing and the use of multiple alternate promoter have been observed, including some splice variants that may be specific to brain and other tissues. An upstream uORF may regulate translation at some splice variants of this gene. [provided by RefSeq, Sep 2018]","start":197042560,"end":197299300,"strand":-1,"description":"discs large MAGUK scaffold protein 1 [Source:HGNC Symbol;Acc:HGNC:2900]"}, {"versioned_ensembl_gene_id":"ENSG00000231471.1","gene_symbol":"HMGN2P34","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39405]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874478","summary":null,"start":72636497,"end":72636765,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:39405]"}, {"versioned_ensembl_gene_id":"ENSG00000255426.1","gene_symbol":"AC044839.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45733994,"end":45735766,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183909.6","gene_symbol":"OR4G2P","gene_name":"olfactory receptor family 4 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8303]","synonyms":"OR4G7P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26680","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101926164,"end":101933350,"strand":-1,"description":"olfactory receptor family 4 subfamily G member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:8303]"}, {"versioned_ensembl_gene_id":"ENSG00000254519.3","gene_symbol":"AC044839.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45722308,"end":45744254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237616.1","gene_symbol":"USP9YP32","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:38776]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480718","summary":null,"start":17995201,"end":17997252,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:38776]"}, {"versioned_ensembl_gene_id":"ENSG00000259217.2","gene_symbol":"AC068867.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35774801,"end":35774950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142166.12","gene_symbol":"IFNAR1","gene_name":"interferon alpha and beta receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:5432]","synonyms":"IFRC,IFNAR","biotype":"protein_coding","ncbi_id":"3454","summary":"The protein encoded by this gene is a type I membrane protein that forms one of the two chains of a receptor for interferons alpha and beta. Binding and activation of the receptor stimulates Janus protein kinases, which in turn phosphorylate several proteins, including STAT1 and STAT2. The protein belongs to the type II cytokine receptor family and functions as an antiviral factor. [provided by RefSeq, Jul 2020]","start":33324477,"end":33359862,"strand":1,"description":"interferon alpha and beta receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:5432]"}, {"versioned_ensembl_gene_id":"ENSG00000189001.10","gene_symbol":"SBSN","gene_name":"suprabasin [Source:HGNC Symbol;Acc:HGNC:24950]","synonyms":"HLAR698,UNQ698","biotype":"protein_coding","ncbi_id":"374897","summary":null,"start":35523367,"end":35528351,"strand":-1,"description":"suprabasin [Source:HGNC Symbol;Acc:HGNC:24950]"}, {"versioned_ensembl_gene_id":"ENSG00000206538.8","gene_symbol":"VGLL3","gene_name":"vestigial like family member 3 [Source:HGNC Symbol;Acc:HGNC:24327]","synonyms":"VGL-3","biotype":"protein_coding","ncbi_id":"389136","summary":null,"start":86876388,"end":86991119,"strand":-1,"description":"vestigial like family member 3 [Source:HGNC Symbol;Acc:HGNC:24327]"}, {"versioned_ensembl_gene_id":"ENSG00000262453.1","gene_symbol":"AL022318.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38921227,"end":38924708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214106.7","gene_symbol":"PAXIP1-AS2","gene_name":"PAXIP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:48958]","synonyms":"PAXIP1OS","biotype":"antisense_RNA","ncbi_id":"100132707","summary":null,"start":154928498,"end":154949908,"strand":1,"description":"PAXIP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:48958]"}, {"versioned_ensembl_gene_id":"ENSG00000224820.2","gene_symbol":"BTF3P4","gene_name":"basic transcription factor 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38566]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392350","summary":null,"start":72107818,"end":72108312,"strand":-1,"description":"basic transcription factor 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38566]"}, {"versioned_ensembl_gene_id":"ENSG00000224240.1","gene_symbol":"CYCSP49","gene_name":"cytochrome c, somatic pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:23943]","synonyms":"HCP49,CYCSP54","biotype":"processed_pseudogene","ncbi_id":"360009","summary":null,"start":26549425,"end":26549743,"strand":1,"description":"cytochrome c, somatic pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:23943]"}, {"versioned_ensembl_gene_id":"ENSG00000004848.7","gene_symbol":"ARX","gene_name":"aristaless related homeobox [Source:HGNC Symbol;Acc:HGNC:18060]","synonyms":"MRX29,ISSX,CT121,EIEE1,PRTS,MRXS1,MRX87,MRX76,MRX54,MRX43,MRX38,MRX36,MRX33,MRX32","biotype":"protein_coding","ncbi_id":"170302","summary":"This gene is a homeobox-containing gene expressed during development. The expressed protein contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Expansion of a polyalanine tract and other mutations in this gene cause X-linked cognitive disability and epilepsy. [provided by RefSeq, Jul 2016]","start":25003694,"end":25016420,"strand":-1,"description":"aristaless related homeobox [Source:HGNC Symbol;Acc:HGNC:18060]"}, {"versioned_ensembl_gene_id":"ENSG00000115738.9","gene_symbol":"ID2","gene_name":"inhibitor of DNA binding 2, HLH protein [Source:HGNC Symbol;Acc:HGNC:5361]","synonyms":"GIG8,bHLHb26","biotype":"protein_coding","ncbi_id":"3398","summary":"The protein encoded by this gene belongs to the inhibitor of DNA binding family, members of which are transcriptional regulators that contain a helix-loop-helix (HLH) domain but not a basic domain. Members of the inhibitor of DNA binding family inhibit the functions of basic helix-loop-helix transcription factors in a dominant-negative manner by suppressing their heterodimerization partners through the HLH domains. This protein may play a role in negatively regulating cell differentiation. A pseudogene of this gene is located on chromosome 3. [provided by RefSeq, Aug 2011]","start":8678845,"end":8684453,"strand":1,"description":"inhibitor of DNA binding 2, HLH protein [Source:HGNC Symbol;Acc:HGNC:5361]"}, {"versioned_ensembl_gene_id":"ENSG00000142609.17","gene_symbol":"CFAP74","gene_name":"cilia and flagella associated protein 74 [Source:HGNC Symbol;Acc:HGNC:29368]","synonyms":"KIAA1751,FLJ45476,C1orf222","biotype":"protein_coding","ncbi_id":"85452","summary":null,"start":1921951,"end":2003837,"strand":-1,"description":"cilia and flagella associated protein 74 [Source:HGNC Symbol;Acc:HGNC:29368]"}, {"versioned_ensembl_gene_id":"ENSG00000281284.1","gene_symbol":"MAPT-IT1","gene_name":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100130148","summary":null,"start":46198938,"end":46201928,"strand":-1,"description":"MAPT intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:43741]"}, {"versioned_ensembl_gene_id":"ENSG00000278194.2","gene_symbol":"SPPL2C","gene_name":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]","synonyms":"IMP5,IMP5","biotype":"protein_coding","ncbi_id":"162540","summary":null,"start":46250606,"end":46252843,"strand":-1,"description":"signal peptide peptidase like 2C [Source:HGNC Symbol;Acc:HGNC:28902]"}, {"versioned_ensembl_gene_id":"ENSG00000235092.5","gene_symbol":"ID2-AS1","gene_name":"ID2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51103]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506299","summary":null,"start":8666636,"end":8681863,"strand":-1,"description":"ID2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51103]"}, {"versioned_ensembl_gene_id":"ENSG00000281139.1","gene_symbol":"STH","gene_name":"saitohin [Source:HGNC Symbol;Acc:HGNC:18839]","synonyms":"MAPTIT","biotype":"protein_coding","ncbi_id":"246744","summary":null,"start":46098193,"end":46098637,"strand":-1,"description":"saitohin [Source:HGNC Symbol;Acc:HGNC:18839]"}, {"versioned_ensembl_gene_id":"ENSG00000223887.10","gene_symbol":"PRR3","gene_name":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]","synonyms":"CAT56,Em:AB023052.2,Em:AB014077.1","biotype":"protein_coding","ncbi_id":"80742","summary":null,"start":30547117,"end":30553954,"strand":1,"description":"proline rich 3 [Source:HGNC Symbol;Acc:HGNC:21149]"}, {"versioned_ensembl_gene_id":"ENSG00000138668.18","gene_symbol":"HNRNPD","gene_name":"heterogeneous nuclear ribonucleoprotein D [Source:HGNC Symbol;Acc:HGNC:5036]","synonyms":"HNRPD,AUF1","biotype":"protein_coding","ncbi_id":"3184","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are nucleic acid binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two repeats of quasi-RRM domains that bind to RNAs. It localizes to both the nucleus and the cytoplasm. This protein is implicated in the regulation of mRNA stability. Alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008]","start":82352498,"end":82374503,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein D [Source:HGNC Symbol;Acc:HGNC:5036]"}, {"versioned_ensembl_gene_id":"ENSG00000233437.1","gene_symbol":"AC118758.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56875385,"end":56882146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178803.10","gene_symbol":"ADORA2A-AS1","gene_name":"ADORA2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37122]","synonyms":"FLJ34651,C22orf45","biotype":"antisense_RNA","ncbi_id":"646023","summary":null,"start":24429206,"end":24495074,"strand":-1,"description":"ADORA2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37122]"}, {"versioned_ensembl_gene_id":"ENSG00000258525.1","gene_symbol":"AL049830.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30876179,"end":30889808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273183.1","gene_symbol":"AC093726.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154956429,"end":154957107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267172.1","gene_symbol":"AC022031.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55817167,"end":55819759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177963.14","gene_symbol":"RIC8A","gene_name":"RIC8 guanine nucleotide exchange factor A [Source:HGNC Symbol;Acc:HGNC:29550]","synonyms":"synembryn-A,synembryn","biotype":"protein_coding","ncbi_id":"60626","summary":null,"start":207511,"end":215113,"strand":1,"description":"RIC8 guanine nucleotide exchange factor A [Source:HGNC Symbol;Acc:HGNC:29550]"}, {"versioned_ensembl_gene_id":"ENSG00000152092.15","gene_symbol":"ASTN1","gene_name":"astrotactin 1 [Source:HGNC Symbol;Acc:HGNC:773]","synonyms":"ASTN","biotype":"protein_coding","ncbi_id":"460","summary":"Astrotactin is a neuronal adhesion molecule required for glial-guided migration of young postmitotic neuroblasts in cortical regions of developing brain, including cerebrum, hippocampus, cerebellum, and olfactory bulb (Fink et al., 1995).[supplied by OMIM, Jun 2009]","start":176857302,"end":177164973,"strand":-1,"description":"astrotactin 1 [Source:HGNC Symbol;Acc:HGNC:773]"}, {"versioned_ensembl_gene_id":"ENSG00000234111.6","gene_symbol":"LINC02433","gene_name":"long intergenic non-protein coding RNA 2433 [Source:HGNC Symbol;Acc:HGNC:27959]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340017","summary":null,"start":157572490,"end":157576154,"strand":1,"description":"long intergenic non-protein coding RNA 2433 [Source:HGNC Symbol;Acc:HGNC:27959]"}, {"versioned_ensembl_gene_id":"ENSG00000232643.1","gene_symbol":"LINC00385","gene_name":"long intergenic non-protein coding RNA 385 [Source:HGNC Symbol;Acc:HGNC:42713]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370141","summary":null,"start":30154066,"end":30154586,"strand":1,"description":"long intergenic non-protein coding RNA 385 [Source:HGNC Symbol;Acc:HGNC:42713]"}, {"versioned_ensembl_gene_id":"ENSG00000133246.11","gene_symbol":"PRAM1","gene_name":"PML-RARA regulated adaptor molecule 1 [Source:HGNC Symbol;Acc:HGNC:30091]","synonyms":"PML-RAR","biotype":"protein_coding","ncbi_id":"84106","summary":"The protein encoded by this gene is similar to FYN binding protein (FYB/SLAP-130), an adaptor protein involved in T cell receptor mediated signaling. This gene is expressed and regulated during normal myelopoiesis. The expression of this gene is induced by retinoic acid and is inhibited by the expression of PML-RARalpha, a fusion protein of promyelocytic leukemia (PML) and the retinoic acid receptor-alpha (RARalpha). [provided by RefSeq, Jul 2008]","start":8490056,"end":8503112,"strand":-1,"description":"PML-RARA regulated adaptor molecule 1 [Source:HGNC Symbol;Acc:HGNC:30091]"}, {"versioned_ensembl_gene_id":"ENSG00000099834.18","gene_symbol":"CDHR5","gene_name":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]","synonyms":"MUCDHL,MU-PCDH,FLJ20219,MUPCDH","biotype":"protein_coding","ncbi_id":"53841","summary":"This gene is a novel mucin-like gene that is a member of the cadherin superfamily. While encoding nonpolymorphic tandem repeats rich in proline, serine and threonine similar to mucin proteins, the gene also contains sequence encoding calcium-binding motifs found in all cadherins. The role of the hybrid extracellular region and the specific function of this protein have not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jan 2010]","start":616565,"end":626078,"strand":-1,"description":"cadherin related family member 5 [Source:HGNC Symbol;Acc:HGNC:7521]"}, {"versioned_ensembl_gene_id":"ENSG00000214018.3","gene_symbol":"RRM2P3","gene_name":"ribonucleotide reductase M2 polypeptide pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420159","summary":null,"start":44309314,"end":44310476,"strand":-1,"description":"ribonucleotide reductase M2 polypeptide pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10455]"}, {"versioned_ensembl_gene_id":"ENSG00000273156.1","gene_symbol":"AC124016.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":82344876,"end":82345540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173597.8","gene_symbol":"SULT1B1","gene_name":"sulfotransferase family 1B member 1 [Source:HGNC Symbol;Acc:HGNC:17845]","synonyms":"ST1B2","biotype":"protein_coding","ncbi_id":"27284","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. However, the total genomic length of this gene is greater than that of other SULT1 genes. [provided by RefSeq, Jul 2008]","start":69721162,"end":69787961,"strand":-1,"description":"sulfotransferase family 1B member 1 [Source:HGNC Symbol;Acc:HGNC:17845]"}, {"versioned_ensembl_gene_id":"ENSG00000028203.17","gene_symbol":"VEZT","gene_name":"vezatin, adherens junctions transmembrane protein [Source:HGNC Symbol;Acc:HGNC:18258]","synonyms":"DKFZP761C241","biotype":"protein_coding","ncbi_id":"55591","summary":"This gene encodes a transmembrane protein which has been localized to adherens junctions and shown to bind to myosin VIIA. Examination of expression of this gene in gastric cancer tissues have shown that expression is decreased which appears to be related to hypermethylation of the promoter. Expression of this gene may also be inhibited by binding of a specific microRNA to a target sequence in the 3' UTR of the transcripts. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]","start":95217746,"end":95302790,"strand":1,"description":"vezatin, adherens junctions transmembrane protein [Source:HGNC Symbol;Acc:HGNC:18258]"}, {"versioned_ensembl_gene_id":"ENSG00000100014.19","gene_symbol":"SPECC1L","gene_name":"sperm antigen with calponin homology and coiled-coil domains 1 like [Source:HGNC Symbol;Acc:HGNC:29022]","synonyms":"KIAA0376,CYTSA","biotype":"protein_coding","ncbi_id":"23384","summary":"This gene encodes a coiled-coil domain containing protein. The encoded protein may play a critical role in actin-cytoskeletal reorganization during facial morphogenesis. Mutations in this gene are a cause of oblique facial clefting-1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A read-through transcript composed of SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1-like) and the downstream ADORA2A (adenosine A2a receptor) gene sequence has been identified, but it is thought to be non-coding. [provided by RefSeq, Jun 2013]","start":24270817,"end":24417740,"strand":1,"description":"sperm antigen with calponin homology and coiled-coil domains 1 like [Source:HGNC Symbol;Acc:HGNC:29022]"}, {"versioned_ensembl_gene_id":"ENSG00000250722.5","gene_symbol":"SELENOP","gene_name":"selenoprotein P [Source:HGNC Symbol;Acc:HGNC:10751]","synonyms":"SEPP1,SEPP,SeP,SELP","biotype":"protein_coding","ncbi_id":"6414","summary":"This gene encodes a selenoprotein that is predominantly expressed in the liver and secreted into the plasma. This selenoprotein is unique in that it contains multiple selenocysteine (Sec) residues per polypeptide (10 in human), and accounts for most of the selenium in plasma. It has been implicated as an extracellular antioxidant, and in the transport of selenium to extra-hepatic tissues via apolipoprotein E receptor-2 (apoER2). Mice lacking this gene exhibit neurological dysfunction, suggesting its importance in normal brain function. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. The mRNA for this selenoprotein contains two SECIS elements. The use of alternative polyadenylation sites, one located in between the two SECIS elements, results in two populations of mRNAs containing either both (predominant) or just the upstream SECIS element (PMID:27881738). Alternatively spliced transcript variants have also been found for this gene. [provided by RefSeq, Oct 2018]","start":42799880,"end":42887392,"strand":-1,"description":"selenoprotein P [Source:HGNC Symbol;Acc:HGNC:10751]"}, {"versioned_ensembl_gene_id":"ENSG00000243403.1","gene_symbol":"AC090543.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64592979,"end":64593326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105647.16","gene_symbol":"PIK3R2","gene_name":"phosphoinositide-3-kinase regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:8980]","synonyms":"P85B,p85","biotype":"protein_coding","ncbi_id":"5296","summary":"Phosphatidylinositol 3-kinase (PI3K) is a lipid kinase that phosphorylates phosphatidylinositol and similar compounds, creating second messengers important in growth signaling pathways. PI3K functions as a heterodimer of a regulatory and a catalytic subunit. The protein encoded by this gene is a regulatory component of PI3K. Three transcript variants, one protein coding and the other two non-protein coding, have been found for this gene. [provided by RefSeq, Apr 2019]","start":18153118,"end":18170540,"strand":1,"description":"phosphoinositide-3-kinase regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:8980]"}, {"versioned_ensembl_gene_id":"ENSG00000274811.3","gene_symbol":"CLPTM1L","gene_name":"CLPTM1 like [Source:HGNC Symbol;Acc:HGNC:24308]","synonyms":"FLJ14400,CRR9","biotype":"protein_coding","ncbi_id":"81037","summary":"The protein encoded by this gene is a membrane protein whose overexpression in cisplatin-sensitive cells causes apoptosis. Polymorphisms in this gene have been reported to increase susceptibility to several cancers, including lung, pancreatic, and breast cancers. [provided by RefSeq, Nov 2015]","start":1318299,"end":1345099,"strand":-1,"description":"CLPTM1 like [Source:HGNC Symbol;Acc:HGNC:24308]"}, {"versioned_ensembl_gene_id":"ENSG00000152078.9","gene_symbol":"TMEM56","gene_name":"transmembrane protein 56 [Source:HGNC Symbol;Acc:HGNC:26477]","synonyms":"FLJ31842","biotype":"protein_coding","ncbi_id":"148534","summary":null,"start":95117338,"end":95197607,"strand":1,"description":"transmembrane protein 56 [Source:HGNC Symbol;Acc:HGNC:26477]"}, {"versioned_ensembl_gene_id":"ENSG00000187608.8","gene_symbol":"ISG15","gene_name":"ISG15 ubiquitin-like modifier [Source:HGNC Symbol;Acc:HGNC:4053]","synonyms":"UCRP,IFI15,G1P2","biotype":"protein_coding","ncbi_id":"9636","summary":"The protein encoded by this gene is a ubiquitin-like protein that is conjugated to intracellular target proteins upon activation by interferon-alpha and interferon-beta. Several functions have been ascribed to the encoded protein, including chemotactic activity towards neutrophils, direction of ligated target proteins to intermediate filaments, cell-to-cell signaling, and antiviral activity during viral infections. While conjugates of this protein have been found to be noncovalently attached to intermediate filaments, this protein is sometimes secreted. [provided by RefSeq, Dec 2012]","start":1001138,"end":1014541,"strand":1,"description":"ISG15 ubiquitin-like modifier [Source:HGNC Symbol;Acc:HGNC:4053]"}, {"versioned_ensembl_gene_id":"ENSG00000163520.13","gene_symbol":"FBLN2","gene_name":"fibulin 2 [Source:HGNC Symbol;Acc:HGNC:3601]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2199","summary":"This gene encodes an extracellular matrix protein, which belongs to the fibulin family. This protein binds various extracellular ligands and calcium. It may play a role during organ development, in particular, during the differentiation of heart, skeletal and neuronal structures. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":13549131,"end":13638422,"strand":1,"description":"fibulin 2 [Source:HGNC Symbol;Acc:HGNC:3601]"}, {"versioned_ensembl_gene_id":"ENSG00000225405.3","gene_symbol":"RPS15AP17","gene_name":"ribosomal protein S15a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36888]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391656","summary":null,"start":62105660,"end":62106049,"strand":-1,"description":"ribosomal protein S15a pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36888]"}, {"versioned_ensembl_gene_id":"ENSG00000265514.1","gene_symbol":"LINC01892","gene_name":"long intergenic non-protein coding RNA 1892 [Source:HGNC Symbol;Acc:HGNC:52711]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371969","summary":null,"start":5081182,"end":5095815,"strand":1,"description":"long intergenic non-protein coding RNA 1892 [Source:HGNC Symbol;Acc:HGNC:52711]"}, {"versioned_ensembl_gene_id":"ENSG00000248692.5","gene_symbol":"ADGRL3-AS1","gene_name":"adhesion G protein-coupled receptor L3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50604]","synonyms":"LPHN3-AS1","biotype":"antisense_RNA","ncbi_id":"101927186","summary":null,"start":62071752,"end":62165554,"strand":-1,"description":"adhesion G protein-coupled receptor L3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50604]"}, {"versioned_ensembl_gene_id":"ENSG00000257894.2","gene_symbol":"AC027288.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79341205,"end":79503396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226439.3","gene_symbol":"AC108161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61775449,"end":61775850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234152.1","gene_symbol":"ELOBP1","gene_name":"elongin B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39719]","synonyms":"TCEB2P1","biotype":"processed_pseudogene","ncbi_id":"246717","summary":null,"start":25365799,"end":25366155,"strand":-1,"description":"elongin B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39719]"}, {"versioned_ensembl_gene_id":"ENSG00000174945.13","gene_symbol":"AMZ1","gene_name":"archaelysin family metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:22231]","synonyms":"KIAA1950","biotype":"protein_coding","ncbi_id":"155185","summary":null,"start":2679522,"end":2775500,"strand":1,"description":"archaelysin family metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:22231]"}, {"versioned_ensembl_gene_id":"ENSG00000078804.12","gene_symbol":"TP53INP2","gene_name":"tumor protein p53 inducible nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16104]","synonyms":"PINH,FLJ23500,FLJ21759,DOR,DKFZp434O0827,DKFZp434B2411,dJ1181N3.1,C20orf110","biotype":"protein_coding","ncbi_id":"58476","summary":"The protein encoded by this gene promotes autophagy and is essential for proper autophagosome formation and processing. In addition, the encoded protein can enhance rDNA transcription by helping in the assembly of the POLR1/RNA polymerase I preinitiation complex. Finally, this protein serves as a transcriptional activator for some genes. [provided by RefSeq, Jul 2016]","start":34704290,"end":34713439,"strand":1,"description":"tumor protein p53 inducible nuclear protein 2 [Source:HGNC Symbol;Acc:HGNC:16104]"}, {"versioned_ensembl_gene_id":"ENSG00000187951.10","gene_symbol":"ARHGAP11B","gene_name":"Rho GTPase activating protein 11B [Source:HGNC Symbol;Acc:HGNC:15782]","synonyms":"B'-T,FAM7B1,B'-T,FAM7B1","biotype":"protein_coding","ncbi_id":"89839","summary":null,"start":30624494,"end":30772993,"strand":1,"description":"Rho GTPase activating protein 11B [Source:HGNC Symbol;Acc:HGNC:15782]"}, {"versioned_ensembl_gene_id":"ENSG00000267238.1","gene_symbol":"AC093074.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28394851,"end":28396428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270275.1","gene_symbol":"TRMT112P7","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44026]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287567","summary":null,"start":54479597,"end":54479963,"strand":-1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44026]"}, {"versioned_ensembl_gene_id":"ENSG00000224794.2","gene_symbol":"AL022326.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39292988,"end":39295589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184274.3","gene_symbol":"LINC00315","gene_name":"long intergenic non-protein coding RNA 315 [Source:HGNC Symbol;Acc:HGNC:16621]","synonyms":"NCRNA00315,C21orf93","biotype":"lincRNA","ncbi_id":"246704","summary":null,"start":45300245,"end":45305257,"strand":-1,"description":"long intergenic non-protein coding RNA 315 [Source:HGNC Symbol;Acc:HGNC:16621]"}, {"versioned_ensembl_gene_id":"ENSG00000273056.1","gene_symbol":"AL354694.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7786105,"end":7786688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274995.1","gene_symbol":"AC013564.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":66740445,"end":66741151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161888.11","gene_symbol":"SPC24","gene_name":"SPC24, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:26913]","synonyms":"SPBC24,FLJ90806","biotype":"protein_coding","ncbi_id":"147841","summary":null,"start":11131520,"end":11155808,"strand":-1,"description":"SPC24, NDC80 kinetochore complex component [Source:HGNC Symbol;Acc:HGNC:26913]"}, {"versioned_ensembl_gene_id":"ENSG00000227652.4","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30476183,"end":30476833,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000204049.1","gene_symbol":"AL391421.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77866875,"end":77869610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230609.1","gene_symbol":"AL513185.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72560264,"end":72560456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254917.1","gene_symbol":"OR7E15P","gene_name":"olfactory receptor family 7 subfamily E member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:8386]","synonyms":"OST001,OR7E80P,OR7E42P,OR11-392","biotype":"unprocessed_pseudogene","ncbi_id":"8588","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":12696307,"end":12697273,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:8386]"}, {"versioned_ensembl_gene_id":"ENSG00000160908.14","gene_symbol":"ZNF394","gene_name":"zinc finger protein 394 [Source:HGNC Symbol;Acc:HGNC:18832]","synonyms":"ZSCAN46,ZKSCAN14,FLJ12298","biotype":"protein_coding","ncbi_id":"84124","summary":"The protein encoded by this gene is a zinc finger protein that inhibits the transcription of mitogen-activated protein kinase signaling pathways. The encoded protein may be involved in cardiac function. [provided by RefSeq, Sep 2016]","start":99486519,"end":99500324,"strand":-1,"description":"zinc finger protein 394 [Source:HGNC Symbol;Acc:HGNC:18832]"}, {"versioned_ensembl_gene_id":"ENSG00000227877.6","gene_symbol":"MRLN","gene_name":"myoregulin [Source:HGNC Symbol;Acc:HGNC:48649]","synonyms":"LINC00948,Linc-RAM,MUSER1,MLN,M1","biotype":"protein_coding","ncbi_id":"100507027","summary":"This gene encodes a small peptide that shares structural similarity to the small peptides sarcolipin and phospholamban, which are key regulators of sarcoplasmic reticulum Ca(2+)-ATPases (SERCAs). This protein is thought to have a similar function to these peptides, regulating Ca(2+) reuptake in the sarcoplasmic reticulum by inhibiting the Ca(2+) pump activity of SERCAs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2015]","start":59736692,"end":59756041,"strand":-1,"description":"myoregulin [Source:HGNC Symbol;Acc:HGNC:48649]"}, {"versioned_ensembl_gene_id":"ENSG00000272940.1","gene_symbol":"U62317.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50597152,"end":50597599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231977.1","gene_symbol":"AL096828.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63166797,"end":63180903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235941.5","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31882493,"end":31884975,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000275713.2","gene_symbol":"HIST1H2BH","gene_name":"histone cluster 1 H2B family member h [Source:HGNC Symbol;Acc:HGNC:4755]","synonyms":"H2BFJ,H2B/j","biotype":"protein_coding","ncbi_id":"8345","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26251651,"end":26253710,"strand":1,"description":"histone cluster 1 H2B family member h [Source:HGNC Symbol;Acc:HGNC:4755]"}, {"versioned_ensembl_gene_id":"ENSG00000235864.1","gene_symbol":"HSPA8P6","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130195","summary":null,"start":209072597,"end":209074148,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44921]"}, {"versioned_ensembl_gene_id":"ENSG00000224104.1","gene_symbol":"AC079809.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153144313,"end":153144588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234800.2","gene_symbol":"PCMTD1P3","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38806]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422595","summary":null,"start":23721311,"end":23721782,"strand":-1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38806]"}, {"versioned_ensembl_gene_id":"ENSG00000258367.2","gene_symbol":"CR383656.14","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18562928,"end":18568790,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214326.2","gene_symbol":"RPL31P1","gene_name":"ribosomal protein L31 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10335]","synonyms":"RPL31P","biotype":"processed_pseudogene","ncbi_id":"54027","summary":null,"start":43551229,"end":43551600,"strand":1,"description":"ribosomal protein L31 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10335]"}, {"versioned_ensembl_gene_id":"ENSG00000249624.8","gene_symbol":"AP000295.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":33246774,"end":33283212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243104.1","gene_symbol":"MTND4LP14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075305","summary":null,"start":120213344,"end":120213631,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:42248]"}, {"versioned_ensembl_gene_id":"ENSG00000182749.5","gene_symbol":"PAQR7","gene_name":"progestin and adipoQ receptor family member 7 [Source:HGNC Symbol;Acc:HGNC:23146]","synonyms":"mSR,MPRA","biotype":"protein_coding","ncbi_id":"164091","summary":null,"start":25861210,"end":25871253,"strand":-1,"description":"progestin and adipoQ receptor family member 7 [Source:HGNC Symbol;Acc:HGNC:23146]"}, {"versioned_ensembl_gene_id":"ENSG00000008311.14","gene_symbol":"AASS","gene_name":"aminoadipate-semialdehyde synthase [Source:HGNC Symbol;Acc:HGNC:17366]","synonyms":"LORSDH,LKRSDH","biotype":"protein_coding","ncbi_id":"10157","summary":"This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia. [provided by RefSeq, Jul 2008]","start":122075647,"end":122144280,"strand":-1,"description":"aminoadipate-semialdehyde synthase [Source:HGNC Symbol;Acc:HGNC:17366]"}, {"versioned_ensembl_gene_id":"ENSG00000117395.12","gene_symbol":"EBNA1BP2","gene_name":"EBNA1 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15531]","synonyms":"P40,NOBP,EBP2","biotype":"protein_coding","ncbi_id":"10969","summary":null,"start":43164175,"end":43270936,"strand":-1,"description":"EBNA1 binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15531]"}, {"versioned_ensembl_gene_id":"ENSG00000064545.14","gene_symbol":"TMEM161A","gene_name":"transmembrane protein 161A [Source:HGNC Symbol;Acc:HGNC:26020]","synonyms":"FLJ39645,FLJ20422","biotype":"protein_coding","ncbi_id":"54929","summary":null,"start":19119169,"end":19138513,"strand":-1,"description":"transmembrane protein 161A [Source:HGNC Symbol;Acc:HGNC:26020]"}, {"versioned_ensembl_gene_id":"ENSG00000276615.2","gene_symbol":"KEL","gene_name":"Kell blood group, metallo-endopeptidase [Source:HGNC Symbol;Acc:HGNC:6308]","synonyms":"ECE3,CD238","biotype":"protein_coding","ncbi_id":"3792","summary":"This gene encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen. The Kell glycoprotein links via a single disulfide bond to the XK membrane protein that carries the Kx antigen. The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases. [provided by RefSeq, Jul 2008]","start":143002301,"end":143023868,"strand":-1,"description":"Kell blood group, metallo-endopeptidase [Source:HGNC Symbol;Acc:HGNC:6308]"}, {"versioned_ensembl_gene_id":"ENSG00000238101.1","gene_symbol":"FAM8A5P","gene_name":"family with sequence similarity 8 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:16376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"114181","summary":null,"start":32629937,"end":32631068,"strand":1,"description":"family with sequence similarity 8 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:16376]"}, {"versioned_ensembl_gene_id":"ENSG00000234498.3","gene_symbol":"RPL13AP20","gene_name":"ribosomal protein L13a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35709]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"387841","summary":null,"start":12875499,"end":12876107,"strand":1,"description":"ribosomal protein L13a pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:35709]"}, {"versioned_ensembl_gene_id":"ENSG00000211790.2","gene_symbol":"TRAV8-4","gene_name":"T-cell receptor alpha variable 8-4 [Source:HGNC Symbol;Acc:HGNC:12149]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28682","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21894433,"end":21895030,"strand":1,"description":"T-cell receptor alpha variable 8-4 [Source:HGNC Symbol;Acc:HGNC:12149]"}, {"versioned_ensembl_gene_id":"ENSG00000213513.3","gene_symbol":"IMPDH1P5","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340780","summary":null,"start":77780337,"end":77781876,"strand":-1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33960]"}, {"versioned_ensembl_gene_id":"ENSG00000265749.5","gene_symbol":"AC135178.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8365563,"end":8381328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137133.10","gene_symbol":"HINT2","gene_name":"histidine triad nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:18344]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84681","summary":"Histidine triad proteins, such as HINT2, are nucleotide hydrolases and transferases that act on the alpha-phosphate of ribonucleotides (Brenner, 2002 [PubMed 12119013]).[supplied by OMIM, Mar 2008]","start":35812960,"end":35815354,"strand":-1,"description":"histidine triad nucleotide binding protein 2 [Source:HGNC Symbol;Acc:HGNC:18344]"}, {"versioned_ensembl_gene_id":"ENSG00000282894.1","gene_symbol":"DUX4L33","gene_name":"double homeobox 4 like 33 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51789]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107080551","summary":null,"start":29324092,"end":29325049,"strand":1,"description":"double homeobox 4 like 33 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51789]"}, {"versioned_ensembl_gene_id":"ENSG00000183778.17","gene_symbol":"B3GALT5","gene_name":"beta-1,3-galactosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:920]","synonyms":"GLCT5,beta3Gal-T5,B3T5,B3GalT-V","biotype":"protein_coding","ncbi_id":"10317","summary":"This gene encodes a member of a family of membrane-bound glycoproteins. The encoded protein may synthesize type 1 Lewis antigens, which are elevated in gastrointestinal and pancreatic cancers. Alternatively spliced transcript variants using multiple alternate promoters have been observed for this gene. [provided by RefSeq, Sep 2017]","start":39556442,"end":39673137,"strand":1,"description":"beta-1,3-galactosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:920]"}, {"versioned_ensembl_gene_id":"ENSG00000228604.3","gene_symbol":"AL121759.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21148741,"end":21162890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214535.3","gene_symbol":"RPS15AP1","gene_name":"ribosomal protein S15a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16598]","synonyms":"dJ872K7.6","biotype":"processed_pseudogene","ncbi_id":"92682","summary":null,"start":21166206,"end":21166596,"strand":-1,"description":"ribosomal protein S15a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16598]"}, {"versioned_ensembl_gene_id":"ENSG00000144057.15","gene_symbol":"ST6GAL2","gene_name":"ST6 beta-galactoside alpha-2,6-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10861]","synonyms":"St6GalII,St6gal2,SIAT2,KIAA1877","biotype":"protein_coding","ncbi_id":"84620","summary":"This locus encodes a sialyltransferase. The encoded type II transmembrane protein catalyzes the transfer of sialic acid from CMP to an oligosaccharide substrate. Polymorphisms at this locus may be associated with variations in risperidone response in schizophrenic patients. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":106801600,"end":106887108,"strand":-1,"description":"ST6 beta-galactoside alpha-2,6-sialyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:10861]"}, {"versioned_ensembl_gene_id":"ENSG00000281432.1","gene_symbol":"AL132642.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93895762,"end":93897759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273024.6","gene_symbol":"INTS4P2","gene_name":"integrator complex subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22351]","synonyms":"MGC133166,INTS4L2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"644619","summary":null,"start":65647823,"end":65718688,"strand":1,"description":"integrator complex subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22351]"}, {"versioned_ensembl_gene_id":"ENSG00000259582.3","gene_symbol":"AC026523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97540597,"end":97560702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224884.1","gene_symbol":"AC034187.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8573726,"end":8593124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237363.1","gene_symbol":"AP006288.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64531044,"end":64532970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142168.14","gene_symbol":"SOD1","gene_name":"superoxide dismutase 1 [Source:HGNC Symbol;Acc:HGNC:11179]","synonyms":"IPOA,ALS1,ALS","biotype":"protein_coding","ncbi_id":"6647","summary":"The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. In addition, this protein contains an antimicrobial peptide that displays antibacterial, antifungal, and anti-MRSA activity against E. coli, E. faecalis, S. aureus, S. aureus MRSA LPV+, S. agalactiae, and yeast C. krusei. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq, Jul 2020]","start":31659622,"end":31668931,"strand":1,"description":"superoxide dismutase 1 [Source:HGNC Symbol;Acc:HGNC:11179]"}, {"versioned_ensembl_gene_id":"ENSG00000276980.1","gene_symbol":"AC008760.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6716386,"end":6717742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281846.1","gene_symbol":"SPATA31E3P","gene_name":"SPATA31 subfamily E member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:43828]","synonyms":"FAM75E3P","biotype":"unprocessed_pseudogene","ncbi_id":"646507","summary":null,"start":22403919,"end":22409655,"strand":1,"description":"SPATA31 subfamily E member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:43828]"}, {"versioned_ensembl_gene_id":"ENSG00000243455.3","gene_symbol":"RPS18P13","gene_name":"ribosomal protein S18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271364","summary":null,"start":18048637,"end":18049090,"strand":1,"description":"ribosomal protein S18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36901]"}, {"versioned_ensembl_gene_id":"ENSG00000234578.1","gene_symbol":"AL355483.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53267935,"end":53268601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169760.17","gene_symbol":"NLGN1","gene_name":"neuroligin 1 [Source:HGNC Symbol;Acc:HGNC:14291]","synonyms":"KIAA1070","biotype":"protein_coding","ncbi_id":"22871","summary":"This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. [provided by RefSeq, Jul 2008]","start":173396284,"end":174286644,"strand":1,"description":"neuroligin 1 [Source:HGNC Symbol;Acc:HGNC:14291]"}, {"versioned_ensembl_gene_id":"ENSG00000235324.4","gene_symbol":"BX649210.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32621929,"end":32622868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225613.2","gene_symbol":"LINCMD1","gene_name":"long intergenic non-protein coding RNA, muscle differentiation 1 [Source:HGNC Symbol;Acc:HGNC:49089]","synonyms":"MIR133BHG,LINC-MD1","biotype":"lincRNA","ncbi_id":"101154644","summary":null,"start":52146814,"end":52151119,"strand":-1,"description":"long intergenic non-protein coding RNA, muscle differentiation 1 [Source:HGNC Symbol;Acc:HGNC:49089]"}, {"versioned_ensembl_gene_id":"ENSG00000233697.2","gene_symbol":"HLA-DRB8","gene_name":"major histocompatibility complex, class II, DR beta 8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4956]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3130","summary":null,"start":32589215,"end":32591752,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 8 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4956]"}, {"versioned_ensembl_gene_id":"ENSG00000268580.1","gene_symbol":"LINC01966","gene_name":"long intergenic non-protein coding RNA 1966 [Source:HGNC Symbol;Acc:HGNC:52792]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373662","summary":null,"start":144877734,"end":144882033,"strand":-1,"description":"long intergenic non-protein coding RNA 1966 [Source:HGNC Symbol;Acc:HGNC:52792]"}, {"versioned_ensembl_gene_id":"ENSG00000261449.1","gene_symbol":"AC103724.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42151772,"end":42152763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277272.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816451,"end":54830756,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000250007.6","gene_symbol":"AC087457.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34755084,"end":34812923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226972.2","gene_symbol":"RPL12P19","gene_name":"ribosomal protein L12 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36248]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129982","summary":null,"start":44270621,"end":44271106,"strand":1,"description":"ribosomal protein L12 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36248]"}, {"versioned_ensembl_gene_id":"ENSG00000076641.4","gene_symbol":"PAG1","gene_name":"phosphoprotein membrane anchor with glycosphingolipid microdomains 1 [Source:HGNC Symbol;Acc:HGNC:30043]","synonyms":"PAG,CBP","biotype":"protein_coding","ncbi_id":"55824","summary":"The protein encoded by this gene is a type III transmembrane adaptor protein that binds to the tyrosine kinase csk protein. It is thought to be involved in the regulation of T cell activation. [provided by RefSeq, Jul 2008]","start":80967810,"end":81112068,"strand":-1,"description":"phosphoprotein membrane anchor with glycosphingolipid microdomains 1 [Source:HGNC Symbol;Acc:HGNC:30043]"}, {"versioned_ensembl_gene_id":"ENSG00000135486.17","gene_symbol":"HNRNPA1","gene_name":"heterogeneous nuclear ribonucleoprotein A1 [Source:HGNC Symbol;Acc:HGNC:5031]","synonyms":"HNRPA1,hnRNPA1,hnRNP-A1,ALS20","biotype":"protein_coding","ncbi_id":"3178","summary":"This gene encodes a member of a family of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs), which are RNA-binding proteins that associate with pre-mRNAs in the nucleus and influence pre-mRNA processing, as well as other aspects of mRNA metabolism and transport. The protein encoded by this gene is one of the most abundant core proteins of hnRNP complexes and plays a key role in the regulation of alternative splicing. Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20. Multiple alternatively spliced transcript variants have been found. There are numerous pseudogenes of this gene distributed throughout the genome. [provided by RefSeq, Feb 2016]","start":54280193,"end":54287088,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 [Source:HGNC Symbol;Acc:HGNC:5031]"}, {"versioned_ensembl_gene_id":"ENSG00000254060.1","gene_symbol":"AC022778.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81036964,"end":81040831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101849.15","gene_symbol":"TBL1X","gene_name":"transducin beta like 1X-linked [Source:HGNC Symbol;Acc:HGNC:11585]","synonyms":"TBL1,EBI","biotype":"protein_coding","ncbi_id":"6907","summary":"The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq, Nov 2008]","start":9463295,"end":9719743,"strand":1,"description":"transducin beta like 1X-linked [Source:HGNC Symbol;Acc:HGNC:11585]"}, {"versioned_ensembl_gene_id":"ENSG00000169908.11","gene_symbol":"TM4SF1","gene_name":"transmembrane 4 L six family member 1 [Source:HGNC Symbol;Acc:HGNC:11853]","synonyms":"M3S1,L6","biotype":"protein_coding","ncbi_id":"4071","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface antigen and is highly expressed in different carcinomas. [provided by RefSeq, Jul 2008]","start":149369022,"end":149377865,"strand":-1,"description":"transmembrane 4 L six family member 1 [Source:HGNC Symbol;Acc:HGNC:11853]"}, {"versioned_ensembl_gene_id":"ENSG00000238102.1","gene_symbol":"AL080248.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7256580,"end":7258214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261249.1","gene_symbol":"LINC01751","gene_name":"long intergenic non-protein coding RNA 1751 [Source:HGNC Symbol;Acc:HGNC:52539]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929288","summary":null,"start":7302056,"end":7307432,"strand":-1,"description":"long intergenic non-protein coding RNA 1751 [Source:HGNC Symbol;Acc:HGNC:52539]"}, {"versioned_ensembl_gene_id":"ENSG00000049192.14","gene_symbol":"ADAMTS6","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 6 [Source:HGNC Symbol;Acc:HGNC:222]","synonyms":"ADAM-TS6","biotype":"protein_coding","ncbi_id":"11174","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. Expression of this gene may be regulated by the cytokine TNF-alpha. [provided by RefSeq, Mar 2016]","start":65148736,"end":65481920,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 6 [Source:HGNC Symbol;Acc:HGNC:222]"}, {"versioned_ensembl_gene_id":"ENSG00000205644.5","gene_symbol":"AC025186.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65415353,"end":65416222,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276613.4","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195747140,"end":195791872,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000228888.1","gene_symbol":"LINC01428","gene_name":"long intergenic non-protein coding RNA 1428 [Source:HGNC Symbol;Acc:HGNC:50738]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929265","summary":null,"start":7146467,"end":7254202,"strand":-1,"description":"long intergenic non-protein coding RNA 1428 [Source:HGNC Symbol;Acc:HGNC:50738]"}, {"versioned_ensembl_gene_id":"ENSG00000234109.1","gene_symbol":"RPL7P36","gene_name":"ribosomal protein L7 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37045]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271218","summary":null,"start":99047639,"end":99048319,"strand":1,"description":"ribosomal protein L7 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:37045]"}, {"versioned_ensembl_gene_id":"ENSG00000206258.12","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"XB,TNXB2,TNXBS,XBS,TNXB1","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32117595,"end":32194037,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000259993.1","gene_symbol":"AC135731.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30223017,"end":30225564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226765.1","gene_symbol":"RPSAP33","gene_name":"ribosomal protein SA pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35556]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647158","summary":null,"start":168666559,"end":168667423,"strand":1,"description":"ribosomal protein SA pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35556]"}, {"versioned_ensembl_gene_id":"ENSG00000241882.1","gene_symbol":"AC124893.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168288553,"end":168291228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262001.1","gene_symbol":"DLGAP1-AS2","gene_name":"DLGAP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:28146]","synonyms":"MGC11082","biotype":"antisense_RNA","ncbi_id":"84777","summary":null,"start":3603000,"end":3608336,"strand":1,"description":"DLGAP1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:28146]"}, {"versioned_ensembl_gene_id":"ENSG00000263724.1","gene_symbol":"DLGAP1-AS3","gene_name":"DLGAP1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:27317]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"201477","summary":null,"start":3878180,"end":3897069,"strand":1,"description":"DLGAP1 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:27317]"}, {"versioned_ensembl_gene_id":"ENSG00000267743.5","gene_symbol":"AC107896.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58189834,"end":58195696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121879.3","gene_symbol":"PIK3CA","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:8975]","synonyms":"PI3K","biotype":"protein_coding","ncbi_id":"5290","summary":"Phosphatidylinositol 3-kinase is composed of an 85 kDa regulatory subunit and a 110 kDa catalytic subunit. The protein encoded by this gene represents the catalytic subunit, which uses ATP to phosphorylate PtdIns, PtdIns4P and PtdIns(4,5)P2. This gene has been found to be oncogenic and has been implicated in cervical cancers. A pseudogene of this gene has been defined on chromosome 22. [provided by RefSeq, Apr 2016]","start":179148114,"end":179240093,"strand":1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:8975]"}, {"versioned_ensembl_gene_id":"ENSG00000224228.2","gene_symbol":"AL031599.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":172775905,"end":173064015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224000.1","gene_symbol":"Z97198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":172906900,"end":172907684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235445.1","gene_symbol":"AC016027.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17983205,"end":17983619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274549.1","gene_symbol":"AL356274.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37139176,"end":37139585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281427.1","gene_symbol":"AC044810.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7783697,"end":7784407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161791.13","gene_symbol":"FMNL3","gene_name":"formin like 3 [Source:HGNC Symbol;Acc:HGNC:23698]","synonyms":"WBP3,MGC45819,DKFZp762B245","biotype":"protein_coding","ncbi_id":"91010","summary":"The protein encoded by this gene contains a formin homology 2 domain and has high sequence identity to the mouse Wbp3 protein. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":49636499,"end":49708165,"strand":-1,"description":"formin like 3 [Source:HGNC Symbol;Acc:HGNC:23698]"}, {"versioned_ensembl_gene_id":"ENSG00000166796.11","gene_symbol":"LDHC","gene_name":"lactate dehydrogenase C [Source:HGNC Symbol;Acc:HGNC:6544]","synonyms":"CT32","biotype":"protein_coding","ncbi_id":"3948","summary":" Lactate dehydrogenase C catalyzes the conversion of L-lactate and NAD to pyruvate and NADH in the final step of anaerobic glycolysis. LDHC is testis-specific and belongs to the lactate dehydrogenase family. Two transcript variants have been detected which differ in the 5' untranslated region. [provided by RefSeq, Jul 2008]","start":18412307,"end":18452058,"strand":1,"description":"lactate dehydrogenase C [Source:HGNC Symbol;Acc:HGNC:6544]"}, {"versioned_ensembl_gene_id":"ENSG00000226808.1","gene_symbol":"LINC00840","gene_name":"long intergenic non-protein coding RNA 840 [Source:HGNC Symbol;Acc:HGNC:44987]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506835","summary":null,"start":43859411,"end":43895433,"strand":1,"description":"long intergenic non-protein coding RNA 840 [Source:HGNC Symbol;Acc:HGNC:44987]"}, {"versioned_ensembl_gene_id":"ENSG00000085832.16","gene_symbol":"EPS15","gene_name":"epidermal growth factor receptor pathway substrate 15 [Source:HGNC Symbol;Acc:HGNC:3419]","synonyms":"MLLT5,AF-1P","biotype":"protein_coding","ncbi_id":"2060","summary":"This gene encodes a protein that is part of the EGFR pathway. The protein is present at clatherin-coated pits and is involved in receptor-mediated endocytosis of EGF. Notably, this gene is rearranged with the HRX/ALL/MLL gene in acute myelogeneous leukemias. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2009]","start":51354263,"end":51519328,"strand":-1,"description":"epidermal growth factor receptor pathway substrate 15 [Source:HGNC Symbol;Acc:HGNC:3419]"}, {"versioned_ensembl_gene_id":"ENSG00000249122.1","gene_symbol":"AC105389.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41750345,"end":41757341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253358.1","gene_symbol":"AC087439.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":91016588,"end":91018655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228109.1","gene_symbol":"MELTF-AS1","gene_name":"MELTF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40373]","synonyms":"MFI2-AS1","biotype":"antisense_RNA","ncbi_id":"100507057","summary":null,"start":196999460,"end":197004744,"strand":1,"description":"MELTF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40373]"}, {"versioned_ensembl_gene_id":"ENSG00000256268.1","gene_symbol":"LINC02454","gene_name":"long intergenic non-protein coding RNA 2454 [Source:HGNC Symbol;Acc:HGNC:53387]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369807","summary":null,"start":65602869,"end":65612997,"strand":1,"description":"long intergenic non-protein coding RNA 2454 [Source:HGNC Symbol;Acc:HGNC:53387]"}, {"versioned_ensembl_gene_id":"ENSG00000248234.1","gene_symbol":"AC091839.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38429892,"end":38430160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238017.1","gene_symbol":"SAPCD1-AS1","gene_name":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]","synonyms":"C6orf26-AS1","biotype":"processed_transcript","ncbi_id":"104413891","summary":null,"start":31751686,"end":31752965,"strand":-1,"description":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]"}, {"versioned_ensembl_gene_id":"ENSG00000283865.1","gene_symbol":"AC073869.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131379743,"end":131380083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173200.12","gene_symbol":"PARP15","gene_name":"poly(ADP-ribose) polymerase family member 15 [Source:HGNC Symbol;Acc:HGNC:26876]","synonyms":"FLJ40597,pART7","biotype":"protein_coding","ncbi_id":"165631","summary":"PARP15 is a macrodomain-containing transcriptional repressor with poly(ADP-ribose) polymerase activity (Aguiar et al., 2005 [PubMed 16061477]).[supplied by OMIM, May 2008]","start":122577602,"end":122639047,"strand":1,"description":"poly(ADP-ribose) polymerase family member 15 [Source:HGNC Symbol;Acc:HGNC:26876]"}, {"versioned_ensembl_gene_id":"ENSG00000233149.10","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFB2,P52,TFIIH","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30952827,"end":30958749,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000235529.1","gene_symbol":"AGAP1-IT1","gene_name":"AGAP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41427]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100506749","summary":null,"start":235505751,"end":235507566,"strand":1,"description":"AGAP1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41427]"}, {"versioned_ensembl_gene_id":"ENSG00000260237.1","gene_symbol":"AC092130.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80040662,"end":80045745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248912.1","gene_symbol":"AC096736.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156686664,"end":156692636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117525.13","gene_symbol":"F3","gene_name":"coagulation factor III, tissue factor [Source:HGNC Symbol;Acc:HGNC:3541]","synonyms":"TF,CD142","biotype":"protein_coding","ncbi_id":"2152","summary":"This gene encodes coagulation factor III which is a cell surface glycoprotein. This factor enables cells to initiate the blood coagulation cascades, and it functions as the high-affinity receptor for the coagulation factor VII. The resulting complex provides a catalytic event that is responsible for initiation of the coagulation protease cascades by specific limited proteolysis. Unlike the other cofactors of these protease cascades, which circulate as nonfunctional precursors, this factor is a potent initiator that is fully functional when expressed on cell surfaces, for example, on monocytes. There are 3 distinct domains of this factor: extracellular, transmembrane, and cytoplasmic. Platelets and monocytes have been shown to express this coagulation factor under procoagulatory and proinflammatory stimuli, and a major role in HIV-associated coagulopathy has been described. Platelet-dependent monocyte expression of coagulation factor III has been described to be associated with Coronavirus Disease 2019 (COVID-19) severity and mortality. This protein is the only one in the coagulation pathway for which a congenital deficiency has not been described. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Aug 2020]","start":94529225,"end":94541800,"strand":-1,"description":"coagulation factor III, tissue factor [Source:HGNC Symbol;Acc:HGNC:3541]"}, {"versioned_ensembl_gene_id":"ENSG00000272430.1","gene_symbol":"AL356056.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46632387,"end":46635472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234208.1","gene_symbol":"AC005529.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29513889,"end":29535390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128463.12","gene_symbol":"EMC4","gene_name":"ER membrane protein complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:28032]","synonyms":"FLJ90746,TMEM85,PIG17,MGC24415","biotype":"protein_coding","ncbi_id":"51234","summary":null,"start":34224999,"end":34230156,"strand":1,"description":"ER membrane protein complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:28032]"}, {"versioned_ensembl_gene_id":"ENSG00000144567.10","gene_symbol":"RETREG2","gene_name":"reticulophagy regulator family member 2 [Source:HGNC Symbol;Acc:HGNC:28450]","synonyms":"MGC3035,MAG-2,FAM134A,C2orf17","biotype":"protein_coding","ncbi_id":"79137","summary":null,"start":219176225,"end":219185479,"strand":1,"description":"reticulophagy regulator family member 2 [Source:HGNC Symbol;Acc:HGNC:28450]"}, {"versioned_ensembl_gene_id":"ENSG00000136694.8","gene_symbol":"IL36A","gene_name":"interleukin 36, alpha [Source:HGNC Symbol;Acc:HGNC:15562]","synonyms":"MGC129553,MGC129552,IL1F6,IL1(EPSILON),IL-1F6,FIL1E,FIL1","biotype":"protein_coding","ncbi_id":"27179","summary":"The protein encoded by this gene is a cytokine that can activate NF-kappa-B and MAPK signaling pathways to generate an inflammatory response. The encoded protein functions primarily in skin and demonstrates increased expression in psoriasis. In addition, decreased expression of this gene has been linked to a poor prognosis in both hepatocellular carcinoma and colorectal cancer patients. [provided by RefSeq, Nov 2015]","start":113005461,"end":113008044,"strand":1,"description":"interleukin 36, alpha [Source:HGNC Symbol;Acc:HGNC:15562]"}, {"versioned_ensembl_gene_id":"ENSG00000244740.1","gene_symbol":"AC092991.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136205540,"end":136205915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204713.10","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RFP,RNF76","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28903002,"end":28923989,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000204128.5","gene_symbol":"C2orf72","gene_name":"chromosome 2 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:27418]","synonyms":"LOC257407","biotype":"protein_coding","ncbi_id":"257407","summary":null,"start":231037490,"end":231049719,"strand":1,"description":"chromosome 2 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:27418]"}, {"versioned_ensembl_gene_id":"ENSG00000140795.12","gene_symbol":"MYLK3","gene_name":"myosin light chain kinase 3 [Source:HGNC Symbol;Acc:HGNC:29826]","synonyms":"MLCK,caMLCK","biotype":"protein_coding","ncbi_id":"91807","summary":"Phosphorylation of cardiac myosin heavy chains (see MYH7B, MIM 609928) and light chains (see MYL2, MIM 160781) by a kinase, such as MYLK3, potentiates the force and rate of cross-bridge recruitment in cardiac myocytes (Chan et al., 2008 [PubMed 18202317]).[supplied by OMIM, Jul 2008]","start":46703369,"end":46790407,"strand":-1,"description":"myosin light chain kinase 3 [Source:HGNC Symbol;Acc:HGNC:29826]"}, {"versioned_ensembl_gene_id":"ENSG00000215398.11","gene_symbol":"CR383658.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18333726,"end":18341859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237390.1","gene_symbol":"AL139130.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156388226,"end":156395609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236737.1","gene_symbol":"GAGE12B","gene_name":"G antigen 12B [Source:HGNC Symbol;Acc:HGNC:26779]","synonyms":"OTTHUMG00000024142","biotype":"protein_coding","ncbi_id":"729428","summary":null,"start":49529869,"end":49529985,"strand":1,"description":"G antigen 12B [Source:HGNC Symbol;Acc:HGNC:26779]"}, {"versioned_ensembl_gene_id":"ENSG00000260955.2","gene_symbol":"AC100821.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54042989,"end":54045629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132664.11","gene_symbol":"POLR3F","gene_name":"RNA polymerase III subunit F [Source:HGNC Symbol;Acc:HGNC:15763]","synonyms":"RPC6,RPC39","biotype":"protein_coding","ncbi_id":"10621","summary":"The protein encoded by this gene is one of more than a dozen subunits forming eukaryotic RNA polymerase III (RNA Pol III), which transcribes 5S ribosomal RNA and tRNA genes. This protein has been shown to bind both TFIIIB90 and TBP, two subunits of RNA polymerase III transcription initiation factor IIIB (TFIIIB). Unlike most of the other RNA Pol III subunits, the encoded protein is unique to this polymerase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":18467127,"end":18484643,"strand":1,"description":"RNA polymerase III subunit F [Source:HGNC Symbol;Acc:HGNC:15763]"}, {"versioned_ensembl_gene_id":"ENSG00000259917.1","gene_symbol":"HNRNPLP2","gene_name":"heterogeneous nuclear ribonucleoprotein L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48747]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644390","summary":null,"start":34489002,"end":34490571,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48747]"}, {"versioned_ensembl_gene_id":"ENSG00000235408.5","gene_symbol":"SNORA71B","gene_name":"small nucleolar RNA, H/ACA box 71B [Source:HGNC Symbol;Acc:HGNC:10233]","synonyms":"U71b,RNU71B","biotype":"snoRNA","ncbi_id":"26776","summary":null,"start":38425083,"end":38425354,"strand":-1,"description":"small nucleolar RNA, H/ACA box 71B [Source:HGNC Symbol;Acc:HGNC:10233]"}, {"versioned_ensembl_gene_id":"ENSG00000234192.1","gene_symbol":"RPS26P38","gene_name":"ribosomal protein S26 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129552","summary":null,"start":87642607,"end":87642954,"strand":1,"description":"ribosomal protein S26 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36406]"}, {"versioned_ensembl_gene_id":"ENSG00000224635.1","gene_symbol":"AL391095.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38406011,"end":38416797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250576.1","gene_symbol":"AC012629.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10775058,"end":10777062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232539.1","gene_symbol":"LINC00945","gene_name":"long intergenic non-protein coding RNA 945 [Source:HGNC Symbol;Acc:HGNC:48643]","synonyms":"TCONS_00028834","biotype":"lincRNA","ncbi_id":"101930746","summary":null,"start":33057829,"end":33064983,"strand":1,"description":"long intergenic non-protein coding RNA 945 [Source:HGNC Symbol;Acc:HGNC:48643]"}, {"versioned_ensembl_gene_id":"ENSG00000276141.4","gene_symbol":"WHAMMP3","gene_name":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27892]","synonyms":"WHDC1L1,WHAMML1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339005","summary":null,"start":22664359,"end":22686213,"strand":1,"description":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27892]"}, {"versioned_ensembl_gene_id":"ENSG00000282159.1","gene_symbol":"AC216089.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101368525,"end":101370831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215529.12","gene_symbol":"EFCAB8","gene_name":"EF-hand calcium binding domain 8 [Source:HGNC Symbol;Acc:HGNC:34532]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388795","summary":null,"start":32858923,"end":32961609,"strand":1,"description":"EF-hand calcium binding domain 8 [Source:HGNC Symbol;Acc:HGNC:34532]"}, {"versioned_ensembl_gene_id":"ENSG00000253720.1","gene_symbol":"AC022973.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129939856,"end":129949394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213412.3","gene_symbol":"HNRNPA1P33","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:44990]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728643","summary":null,"start":46415853,"end":46416413,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:44990]"}, {"versioned_ensembl_gene_id":"ENSG00000203971.1","gene_symbol":"AL354984.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57957126,"end":57959660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230209.1","gene_symbol":"HNRNPA1P2","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]","synonyms":"HNRPA1P2,dJ372B18.1","biotype":"processed_pseudogene","ncbi_id":"100131609","summary":null,"start":32301091,"end":32302050,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:13958]"}, {"versioned_ensembl_gene_id":"ENSG00000227383.1","gene_symbol":"AL353662.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34191555,"end":34191881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228159.1","gene_symbol":"LINC01674","gene_name":"long intergenic non-protein coding RNA 1674 [Source:HGNC Symbol;Acc:HGNC:52462]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724188","summary":null,"start":13546033,"end":13558461,"strand":1,"description":"long intergenic non-protein coding RNA 1674 [Source:HGNC Symbol;Acc:HGNC:52462]"}, {"versioned_ensembl_gene_id":"ENSG00000234731.2","gene_symbol":"MTND4LP16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42250]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075210","summary":null,"start":201554096,"end":201554390,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42250]"}, {"versioned_ensembl_gene_id":"ENSG00000235595.1","gene_symbol":"GAPDHP23","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391075","summary":null,"start":119462029,"end":119463021,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37775]"}, {"versioned_ensembl_gene_id":"ENSG00000259844.2","gene_symbol":"AC018555.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60654235,"end":60656649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250470.1","gene_symbol":"AC253536.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23976904,"end":23977585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274970.1","gene_symbol":"AC013470.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12439419,"end":12440404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251339.5","gene_symbol":"AC017091.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58780626,"end":58984152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111241.2","gene_symbol":"FGF6","gene_name":"fibroblast growth factor 6 [Source:HGNC Symbol;Acc:HGNC:3684]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2251","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene displayed oncogenic transforming activity when transfected into mammalian cells. The mouse homolog of this gene exhibits a restricted expression profile predominantly in the myogenic lineage, which suggested a role in muscle regeneration or differentiation. [provided by RefSeq, Jul 2008]","start":4428155,"end":4445614,"strand":-1,"description":"fibroblast growth factor 6 [Source:HGNC Symbol;Acc:HGNC:3684]"}, {"versioned_ensembl_gene_id":"ENSG00000196182.10","gene_symbol":"STK40","gene_name":"serine/threonine kinase 40 [Source:HGNC Symbol;Acc:HGNC:21373]","synonyms":"SgK495,MGC4796","biotype":"protein_coding","ncbi_id":"83931","summary":null,"start":36339624,"end":36385896,"strand":-1,"description":"serine/threonine kinase 40 [Source:HGNC Symbol;Acc:HGNC:21373]"}, {"versioned_ensembl_gene_id":"ENSG00000178596.10","gene_symbol":"GAPDHP29","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:37781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441893","summary":null,"start":94302038,"end":94303022,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:37781]"}, {"versioned_ensembl_gene_id":"ENSG00000132394.10","gene_symbol":"EEFSEC","gene_name":"eukaryotic elongation factor, selenocysteine-tRNA specific [Source:HGNC Symbol;Acc:HGNC:24614]","synonyms":"EFSEC,eEFSec,SELB","biotype":"protein_coding","ncbi_id":"60678","summary":null,"start":128153454,"end":128408646,"strand":1,"description":"eukaryotic elongation factor, selenocysteine-tRNA specific [Source:HGNC Symbol;Acc:HGNC:24614]"}, {"versioned_ensembl_gene_id":"ENSG00000255714.1","gene_symbol":"LINC02460","gene_name":"long intergenic non-protein coding RNA 2460 [Source:HGNC Symbol;Acc:HGNC:53396]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370013","summary":null,"start":118645315,"end":118648724,"strand":-1,"description":"long intergenic non-protein coding RNA 2460 [Source:HGNC Symbol;Acc:HGNC:53396]"}, {"versioned_ensembl_gene_id":"ENSG00000263090.5","gene_symbol":"KRTAP9-2","gene_name":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]","synonyms":"KAP9.2","biotype":"protein_coding","ncbi_id":"83899","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41226648,"end":41227652,"strand":1,"description":"keratin associated protein 9-2 [Source:HGNC Symbol;Acc:HGNC:16926]"}, {"versioned_ensembl_gene_id":"ENSG00000106479.10","gene_symbol":"ZNF862","gene_name":"zinc finger protein 862 [Source:HGNC Symbol;Acc:HGNC:34519]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643641","summary":null,"start":149838367,"end":149867479,"strand":1,"description":"zinc finger protein 862 [Source:HGNC Symbol;Acc:HGNC:34519]"}, {"versioned_ensembl_gene_id":"ENSG00000263307.1","gene_symbol":"AC007216.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11851649,"end":11895611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216902.3","gene_symbol":"AL122016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85257328,"end":85257694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255769.7","gene_symbol":"GOLGA2P10","gene_name":"golgin A2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:26229]","synonyms":"FLJ22795,AgSK1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"80154","summary":null,"start":82472993,"end":82513950,"strand":-1,"description":"golgin A2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:26229]"}, {"versioned_ensembl_gene_id":"ENSG00000255254.1","gene_symbol":"HIGD1AP5","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42999]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289300","summary":null,"start":18106583,"end":18106841,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42999]"}, {"versioned_ensembl_gene_id":"ENSG00000276710.4","gene_symbol":"CSPG4P10","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48361]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390627","summary":null,"start":82459472,"end":82477258,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48361]"}, {"versioned_ensembl_gene_id":"ENSG00000223482.7","gene_symbol":"NUTM2A-AS1","gene_name":"NUTM2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45161]","synonyms":"FAM22A-AS1","biotype":"antisense_RNA","ncbi_id":"728190","summary":null,"start":87203875,"end":87342612,"strand":-1,"description":"NUTM2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45161]"}, {"versioned_ensembl_gene_id":"ENSG00000257539.2","gene_symbol":"HSPA8P14","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642580","summary":null,"start":111381867,"end":111385638,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:44929]"}, {"versioned_ensembl_gene_id":"ENSG00000184507.15","gene_symbol":"NUTM1","gene_name":"NUT midline carcinoma family member 1 [Source:HGNC Symbol;Acc:HGNC:29919]","synonyms":"NUT,FAM22H,DKFZp434O192,C15orf55","biotype":"protein_coding","ncbi_id":"256646","summary":null,"start":34343315,"end":34357737,"strand":1,"description":"NUT midline carcinoma family member 1 [Source:HGNC Symbol;Acc:HGNC:29919]"}, {"versioned_ensembl_gene_id":"ENSG00000231961.1","gene_symbol":"AL035461.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5965180,"end":5965511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259261.2","gene_symbol":"IGHV4OR15-8","gene_name":"immunoglobulin heavy variable 4/OR15-8 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5658]","synonyms":"VSIG6,IGHV4OR158,IGHV4/OR15-8","biotype":"IG_V_gene","ncbi_id":"28317","summary":null,"start":22184967,"end":22185402,"strand":-1,"description":"immunoglobulin heavy variable 4/OR15-8 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5658]"}, {"versioned_ensembl_gene_id":"ENSG00000260739.1","gene_symbol":"AC010760.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22145939,"end":22148226,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102967.11","gene_symbol":"DHODH","gene_name":"dihydroorotate dehydrogenase (quinone) [Source:HGNC Symbol;Acc:HGNC:2867]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1723","summary":"The protein encoded by this gene catalyzes the fourth enzymatic step, the ubiquinone-mediated oxidation of dihydroorotate to orotate, in de novo pyrimidine biosynthesis. This protein is a mitochondrial protein located on the outer surface of the inner mitochondrial membrane. [provided by RefSeq, Jul 2008]","start":72008588,"end":72027664,"strand":1,"description":"dihydroorotate dehydrogenase (quinone) [Source:HGNC Symbol;Acc:HGNC:2867]"}, {"versioned_ensembl_gene_id":"ENSG00000139173.9","gene_symbol":"TMEM117","gene_name":"transmembrane protein 117 [Source:HGNC Symbol;Acc:HGNC:25308]","synonyms":"DKFZp434K2435","biotype":"protein_coding","ncbi_id":"84216","summary":null,"start":43835967,"end":44389762,"strand":1,"description":"transmembrane protein 117 [Source:HGNC Symbol;Acc:HGNC:25308]"}, {"versioned_ensembl_gene_id":"ENSG00000198298.12","gene_symbol":"ZNF485","gene_name":"zinc finger protein 485 [Source:HGNC Symbol;Acc:HGNC:23440]","synonyms":null,"biotype":"protein_coding","ncbi_id":"220992","summary":null,"start":43606407,"end":43617903,"strand":1,"description":"zinc finger protein 485 [Source:HGNC Symbol;Acc:HGNC:23440]"}, {"versioned_ensembl_gene_id":"ENSG00000153233.12","gene_symbol":"PTPRR","gene_name":"protein tyrosine phosphatase, receptor type R [Source:HGNC Symbol;Acc:HGNC:9680]","synonyms":"PTPRQ,PTPBR7,PTP-SL,PCPTP1,EC-PTP","biotype":"protein_coding","ncbi_id":"5801","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single intracellular catalytic domain, and thus represents a receptor-type PTP. Silencing of this gene has been associated with colorectal cancer. Multiple transcript variants encoding different isoforms have been found for this gene. This gene shares a symbol (PTPRQ) with another gene, protein tyrosine phosphatase, receptor type, Q (GeneID 374462), which is also located on chromosome 12. [provided by RefSeq, May 2011]","start":70638073,"end":70920843,"strand":-1,"description":"protein tyrosine phosphatase, receptor type R [Source:HGNC Symbol;Acc:HGNC:9680]"}, {"versioned_ensembl_gene_id":"ENSG00000237128.1","gene_symbol":"AL358234.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28433008,"end":28495813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263450.1","gene_symbol":"AC090371.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32954075,"end":32957998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272944.1","gene_symbol":"AC079834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":221572506,"end":221574454,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243355.1","gene_symbol":"AC012123.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32779039,"end":32779286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236456.1","gene_symbol":"AL035458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34245953,"end":34246537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214185.3","gene_symbol":"XPOTP1","gene_name":"exportin for tRNA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16586]","synonyms":"XPO3P1,dJ785G19.1","biotype":"processed_pseudogene","ncbi_id":"170559","summary":null,"start":34213495,"end":34215892,"strand":-1,"description":"exportin for tRNA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16586]"}, {"versioned_ensembl_gene_id":"ENSG00000277436.1","gene_symbol":"REXO1L5P","gene_name":"REXO1 like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32242]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107986879","summary":null,"start":85814767,"end":85818783,"strand":-1,"description":"REXO1 like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:32242]"}, {"versioned_ensembl_gene_id":"ENSG00000172172.7","gene_symbol":"MRPL13","gene_name":"mitochondrial ribosomal protein L13 [Source:HGNC Symbol;Acc:HGNC:14278]","synonyms":"RPML13,RPL13,L13mt,L13A,L13","biotype":"protein_coding","ncbi_id":"28998","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":120380761,"end":120445402,"strand":-1,"description":"mitochondrial ribosomal protein L13 [Source:HGNC Symbol;Acc:HGNC:14278]"}, {"versioned_ensembl_gene_id":"ENSG00000226442.2","gene_symbol":"AC006037.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":234109081,"end":234109481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253250.2","gene_symbol":"C8orf88","gene_name":"chromosome 8 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:44672]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100127983","summary":null,"start":90958637,"end":90985257,"strand":-1,"description":"chromosome 8 open reading frame 88 [Source:HGNC Symbol;Acc:HGNC:44672]"}, {"versioned_ensembl_gene_id":"ENSG00000124731.12","gene_symbol":"TREM1","gene_name":"triggering receptor expressed on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:17760]","synonyms":"TREM-1,CD354","biotype":"protein_coding","ncbi_id":"54210","summary":"This gene encodes a receptor belonging to the Ig superfamily that is expressed on myeloid cells. This protein amplifies neutrophil and monocyte-mediated inflammatory responses triggered by bacterial and fungal infections by stimulating release of pro-inflammatory chemokines and cytokines, as well as increased surface expression of cell activation markers. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jun 2011]","start":41267926,"end":41286719,"strand":-1,"description":"triggering receptor expressed on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:17760]"}, {"versioned_ensembl_gene_id":"ENSG00000232838.3","gene_symbol":"PET117","gene_name":"PET117 homolog [Source:HGNC Symbol;Acc:HGNC:40045]","synonyms":"CSRP2BP","biotype":"protein_coding","ncbi_id":"100303755","summary":null,"start":18137873,"end":18143169,"strand":1,"description":"PET117 homolog [Source:HGNC Symbol;Acc:HGNC:40045]"}, {"versioned_ensembl_gene_id":"ENSG00000041353.9","gene_symbol":"RAB27B","gene_name":"RAB27B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9767]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5874","summary":"Members of the Rab protein family, including RAB27B, are prenylated, membrane-bound proteins involved in vesicular fusion and trafficking (Chen et al., 1997 [PubMed 9066979]).[supplied by OMIM, Nov 2010]","start":54717860,"end":54895516,"strand":1,"description":"RAB27B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9767]"}, {"versioned_ensembl_gene_id":"ENSG00000242178.1","gene_symbol":"MTND4P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42204]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873242","summary":null,"start":166160021,"end":166160370,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:42204]"}, {"versioned_ensembl_gene_id":"ENSG00000114030.12","gene_symbol":"KPNA1","gene_name":"karyopherin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6394]","synonyms":"SRP1,RCH2,NPI-1,IPOA5","biotype":"protein_coding","ncbi_id":"3836","summary":"The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC), which consists of 60-100 proteins. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion while larger molecules are transported by an active process. The protein encoded by this gene belongs to the importin alpha family, and is involved in nuclear protein import. This protein interacts with the recombination activating gene 1 (RAG1) protein and is a putative substrate of the RAG1 ubiquitin ligase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":122421949,"end":122514945,"strand":-1,"description":"karyopherin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6394]"}, {"versioned_ensembl_gene_id":"ENSG00000123119.11","gene_symbol":"NECAB1","gene_name":"N-terminal EF-hand calcium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:20983]","synonyms":"EFCBP1","biotype":"protein_coding","ncbi_id":"64168","summary":null,"start":90791550,"end":90959408,"strand":1,"description":"N-terminal EF-hand calcium binding protein 1 [Source:HGNC Symbol;Acc:HGNC:20983]"}, {"versioned_ensembl_gene_id":"ENSG00000111490.12","gene_symbol":"TBC1D30","gene_name":"TBC1 domain family member 30 [Source:HGNC Symbol;Acc:HGNC:29164]","synonyms":"KIAA0984","biotype":"protein_coding","ncbi_id":"23329","summary":null,"start":64781193,"end":64881032,"strand":1,"description":"TBC1 domain family member 30 [Source:HGNC Symbol;Acc:HGNC:29164]"}, {"versioned_ensembl_gene_id":"ENSG00000184984.9","gene_symbol":"CHRM5","gene_name":"cholinergic receptor muscarinic 5 [Source:HGNC Symbol;Acc:HGNC:1954]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1133","summary":"The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The clinical implications of this receptor are unknown; however, stimulation of this receptor is known to increase cyclic AMP levels. [provided by RefSeq, Jul 2008]","start":33968720,"end":34067457,"strand":1,"description":"cholinergic receptor muscarinic 5 [Source:HGNC Symbol;Acc:HGNC:1954]"}, {"versioned_ensembl_gene_id":"ENSG00000233504.1","gene_symbol":"POLR2LP1","gene_name":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]","synonyms":"AB023060.6,POLR2LP","biotype":"processed_pseudogene","ncbi_id":"493825","summary":null,"start":31219263,"end":31219449,"strand":1,"description":"RNA polymerase II subunit L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31340]"}, {"versioned_ensembl_gene_id":"ENSG00000114349.9","gene_symbol":"GNAT1","gene_name":"G protein subunit alpha transducin 1 [Source:HGNC Symbol;Acc:HGNC:4393]","synonyms":"CSNBAD3","biotype":"protein_coding","ncbi_id":"2779","summary":"Transducin is a 3-subunit guanine nucleotide-binding protein (G protein) which stimulates the coupling of rhodopsin and cGMP-phoshodiesterase during visual impulses. The transducin alpha subunits in rods and cones are encoded by separate genes. This gene encodes the alpha subunit in rods. This gene is also expressed in other cells, and has been implicated in bitter taste transduction in rat taste cells. Mutations in this gene result in autosomal dominant congenital stationary night blindness. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2009]","start":50191612,"end":50196516,"strand":1,"description":"G protein subunit alpha transducin 1 [Source:HGNC Symbol;Acc:HGNC:4393]"}, {"versioned_ensembl_gene_id":"ENSG00000105613.9","gene_symbol":"MAST1","gene_name":"microtubule associated serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:19034]","synonyms":"SAST,KIAA0973","biotype":"protein_coding","ncbi_id":"22983","summary":"This gene is a member of the microtubule-associated serine/threonine kinase (MAST) family. The protein encoded by this gene has an N-terminal serine/threonine kinase domain followed by a postsynaptic density protein-95/discs large/zona occludens-1 (PDZ) domain. In mouse and rat, the orthologous protein associates with the cytoskeleton and can bind both beta-2-syntrophin and neuronal nitric oxide synthase (nNOS) through its PDZ domain. In mouse and rat, this protein also co-localizes with dystrophin- and utrophin-associated protein complexes (DAPC/UAPC) in the vascular endothelium of the central nervous system. [provided by RefSeq, May 2017]","start":12833951,"end":12874951,"strand":1,"description":"microtubule associated serine/threonine kinase 1 [Source:HGNC Symbol;Acc:HGNC:19034]"}, {"versioned_ensembl_gene_id":"ENSG00000254240.1","gene_symbol":"IGLVI-20","gene_name":"immunoglobulin lambda variable (I)-20 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5934]","synonyms":"IGLV(I)-20","biotype":"IG_V_pseudogene","ncbi_id":"28769","summary":null,"start":22715290,"end":22715419,"strand":1,"description":"immunoglobulin lambda variable (I)-20 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5934]"}, {"versioned_ensembl_gene_id":"ENSG00000227657.1","gene_symbol":"SERPINA7P1","gene_name":"serpin family A member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44398]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422644","summary":null,"start":106562774,"end":106563404,"strand":-1,"description":"serpin family A member 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44398]"}, {"versioned_ensembl_gene_id":"ENSG00000254866.2","gene_symbol":"DEFB109D","gene_name":"defensin beta 109D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30838]","synonyms":"DEFB109P3","biotype":"processed_pseudogene","ncbi_id":"503838","summary":null,"start":12150895,"end":12151134,"strand":-1,"description":"defensin beta 109D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30838]"}, {"versioned_ensembl_gene_id":"ENSG00000234493.3","gene_symbol":"RHOXF1P1","gene_name":"Rhox homeobox family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51580]","synonyms":"TCONS_00017086","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101928941","summary":null,"start":120010718,"end":120015544,"strand":-1,"description":"Rhox homeobox family member 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51580]"}, {"versioned_ensembl_gene_id":"ENSG00000185917.13","gene_symbol":"SETD4","gene_name":"SET domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1258]","synonyms":"C21orf27,C21orf18","biotype":"protein_coding","ncbi_id":"54093","summary":null,"start":36034541,"end":36079389,"strand":-1,"description":"SET domain containing 4 [Source:HGNC Symbol;Acc:HGNC:1258]"}, {"versioned_ensembl_gene_id":"ENSG00000280115.1","gene_symbol":"AC136603.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78872739,"end":78873505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254180.1","gene_symbol":"AB015752.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90534611,"end":90620070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205879.5","gene_symbol":"FAM90A2P","gene_name":"family with sequence similarity 90 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32250]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729689","summary":null,"start":12172761,"end":12175771,"strand":-1,"description":"family with sequence similarity 90 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:32250]"}, {"versioned_ensembl_gene_id":"ENSG00000259771.1","gene_symbol":"AC092756.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":59266720,"end":59271162,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261852.3","gene_symbol":"KRTAP2-1","gene_name":"keratin associated protein 2-1 [Source:HGNC Symbol;Acc:HGNC:16775]","synonyms":"KAP2.1A","biotype":"protein_coding","ncbi_id":"81872","summary":null,"start":41046666,"end":41047441,"strand":-1,"description":"keratin associated protein 2-1 [Source:HGNC Symbol;Acc:HGNC:16775]"}, {"versioned_ensembl_gene_id":"ENSG00000259732.1","gene_symbol":"AC092757.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":59121034,"end":59133250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248161.5","gene_symbol":"AC098487.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102418602,"end":102450010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259735.1","gene_symbol":"AC092868.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":59348648,"end":59359889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101890.4","gene_symbol":"GUCY2F","gene_name":"guanylate cyclase 2F, retinal [Source:HGNC Symbol;Acc:HGNC:4691]","synonyms":"ROS-GC2,RetGC-2,GUC2DL,GC-F,CYGF","biotype":"protein_coding","ncbi_id":"2986","summary":"The protein encoded by this gene is a guanylyl cyclase found predominantly in photoreceptors in the retina. The encoded protein is thought to be involved in resynthesis of cGMP after light activation of the visual signal transduction cascade, allowing a return to the dark state. This protein is a single-pass type I membrane protein. Defects in this gene may be a cause of X-linked retinitis pigmentosa. [provided by RefSeq, Dec 2008]","start":109372906,"end":109482072,"strand":-1,"description":"guanylate cyclase 2F, retinal [Source:HGNC Symbol;Acc:HGNC:4691]"}, {"versioned_ensembl_gene_id":"ENSG00000284071.1","gene_symbol":"AC012005.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24196518,"end":24206132,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223387.6","gene_symbol":"LINC02068","gene_name":"long intergenic non-protein coding RNA 2068 [Source:HGNC Symbol;Acc:HGNC:52914]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374219","summary":null,"start":172560888,"end":172595607,"strand":-1,"description":"long intergenic non-protein coding RNA 2068 [Source:HGNC Symbol;Acc:HGNC:52914]"}, {"versioned_ensembl_gene_id":"ENSG00000128512.20","gene_symbol":"DOCK4","gene_name":"dedicator of cytokinesis 4 [Source:HGNC Symbol;Acc:HGNC:19192]","synonyms":"KIAA0716,FLJ34238","biotype":"protein_coding","ncbi_id":"9732","summary":"This gene is a member of the dedicator of cytokinesis (DOCK) family and encodes a protein with a DHR-1 (CZH-1) domain, a DHR-2 (CZH-2) domain and an SH3 domain. This membrane-associated, cytoplasmic protein functions as a guanine nucleotide exchange factor and is involved in regulation of adherens junctions between cells. Mutations in this gene have been associated with ovarian, prostate, glioma, and colorectal cancers. Alternatively spliced variants which encode different protein isoforms have been described, but only one has been fully characterized. [provided by RefSeq, Jul 2008]","start":111726110,"end":112206411,"strand":-1,"description":"dedicator of cytokinesis 4 [Source:HGNC Symbol;Acc:HGNC:19192]"}, {"versioned_ensembl_gene_id":"ENSG00000171989.5","gene_symbol":"LDHAL6B","gene_name":"lactate dehydrogenase A like 6B [Source:HGNC Symbol;Acc:HGNC:21481]","synonyms":"LDHL,LDHAL6,LDH6B","biotype":"protein_coding","ncbi_id":"92483","summary":null,"start":59206823,"end":59208515,"strand":1,"description":"lactate dehydrogenase A like 6B [Source:HGNC Symbol;Acc:HGNC:21481]"}, {"versioned_ensembl_gene_id":"ENSG00000225402.1","gene_symbol":"AC010878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37816915,"end":37817961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188687.17","gene_symbol":"SLC4A5","gene_name":"solute carrier family 4 member 5 [Source:HGNC Symbol;Acc:HGNC:18168]","synonyms":"NBC4","biotype":"protein_coding","ncbi_id":"57835","summary":"This gene encodes a member of the sodium bicarbonate cotransporter (NBC) family, part of the bicarbonate transporter superfamily. Sodium bicarbonate cotransporters are involved in intracellular pH regulation and electroneural or electrogenic sodium bicarbonate transport. This protein is thought to be an integral membrane protein. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]","start":74216242,"end":74343414,"strand":-1,"description":"solute carrier family 4 member 5 [Source:HGNC Symbol;Acc:HGNC:18168]"}, {"versioned_ensembl_gene_id":"ENSG00000254700.1","gene_symbol":"DEFB131C","gene_name":"defensin beta 131C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38060]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128174","summary":null,"start":12043506,"end":12043670,"strand":-1,"description":"defensin beta 131C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38060]"}, {"versioned_ensembl_gene_id":"ENSG00000259674.1","gene_symbol":"AC092868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59406963,"end":59408154,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262731.3","gene_symbol":"AC037482.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41054623,"end":41055489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225898.1","gene_symbol":"AC002075.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93777839,"end":93778514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157483.8","gene_symbol":"MYO1E","gene_name":"myosin IE [Source:HGNC Symbol;Acc:HGNC:7599]","synonyms":"MYO1C,MGC104638,HuncM-IC","biotype":"protein_coding","ncbi_id":"4643","summary":"This gene encodes a member of the nonmuscle class I myosins which are a subgroup of the unconventional myosin protein family. The unconventional myosin proteins function as actin-based molecular motors. Class I myosins are characterized by a head (motor) domain, a regulatory domain and a either a short or long tail domain. Among the class I myosins, this protein is distinguished by a long tail domain that is involved in crosslinking actin filaments. This protein localizes to the cytoplasm and may be involved in intracellular movement and membrane trafficking. Mutations in this gene are the cause of focal segmental glomerulosclerosis-6. This gene has been referred to as myosin IC in the literature but is distinct from the myosin IC gene located on chromosome 17. [provided by RefSeq, Jan 2012]","start":59132434,"end":59372900,"strand":-1,"description":"myosin IE [Source:HGNC Symbol;Acc:HGNC:7599]"}, {"versioned_ensembl_gene_id":"ENSG00000234695.1","gene_symbol":"AC002076.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93890913,"end":93893601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101846.6","gene_symbol":"STS","gene_name":"steroid sulfatase [Source:HGNC Symbol;Acc:HGNC:11425]","synonyms":"ARSC1,ARSC","biotype":"protein_coding","ncbi_id":"412","summary":"This gene encodes a multi-pass membrane protein that is localized to the endoplasmic reticulum. It belongs to the sulfatase family and hydrolyzes several 3-beta-hydroxysteroid sulfates, which serve as metabolic precursors for estrogens, androgens, and cholesterol. Mutations in this gene are associated with X-linked ichthyosis (XLI). Alternatively spliced transcript variants resulting from the use of different promoters have been described for this gene (PMID:17601726). [provided by RefSeq, Mar 2016]","start":7219456,"end":7354810,"strand":1,"description":"steroid sulfatase [Source:HGNC Symbol;Acc:HGNC:11425]"}, {"versioned_ensembl_gene_id":"ENSG00000275120.2","gene_symbol":"AC048382.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84597809,"end":84633987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127928.12","gene_symbol":"GNGT1","gene_name":"G protein subunit gamma transducin 1 [Source:HGNC Symbol;Acc:HGNC:4411]","synonyms":"GNG1","biotype":"protein_coding","ncbi_id":"2792","summary":"This gene encodes the gamma subunit of transducin, a guanine nucleotide-binding protein (G protein) that is found in rod outer segments. Transducin, also known as GMPase, mediates the activation of a cyclic GTP-specific (guanosine monophosphate) phosphodiesterase by rhodopsin. [provided by RefSeq, Jul 2016]","start":93591573,"end":93911265,"strand":1,"description":"G protein subunit gamma transducin 1 [Source:HGNC Symbol;Acc:HGNC:4411]"}, {"versioned_ensembl_gene_id":"ENSG00000107521.18","gene_symbol":"HPS1","gene_name":"HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 [Source:HGNC Symbol;Acc:HGNC:5163]","synonyms":"HPS,BLOC3S1","biotype":"protein_coding","ncbi_id":"3257","summary":"This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is a component of three different protein complexes termed biogenesis of lysosome-related organelles complex (BLOC)-3, BLOC4, and BLOC5. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 1. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on chromosome 22. [provided by RefSeq, Aug 2015]","start":98416198,"end":98446947,"strand":-1,"description":"HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 [Source:HGNC Symbol;Acc:HGNC:5163]"}, {"versioned_ensembl_gene_id":"ENSG00000229262.1","gene_symbol":"AL160411.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18059493,"end":18071008,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256278.1","gene_symbol":"AC048382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84611689,"end":84614969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274139.1","gene_symbol":"AC090164.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":101495052,"end":101495567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259172.1","gene_symbol":"AC023024.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101295419,"end":101305737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227343.1","gene_symbol":"RPL15P1","gene_name":"ribosomal protein L15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16583]","synonyms":"dJ726N1.3","biotype":"processed_pseudogene","ncbi_id":"128756","summary":null,"start":18090116,"end":18090715,"strand":-1,"description":"ribosomal protein L15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16583]"}, {"versioned_ensembl_gene_id":"ENSG00000259764.1","gene_symbol":"PCSK6-AS1","gene_name":"PCSK6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51448]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105371027","summary":null,"start":101334437,"end":101337428,"strand":1,"description":"PCSK6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51448]"}, {"versioned_ensembl_gene_id":"ENSG00000177082.12","gene_symbol":"WDR73","gene_name":"WD repeat domain 73 [Source:HGNC Symbol;Acc:HGNC:25928]","synonyms":"HSPC264,FLJ14888","biotype":"protein_coding","ncbi_id":"84942","summary":"The protein encoded by this gene is thought to contain multiple WD40 repeats. WD40 repeats are motifs that contain 40-60 amino acids, and usually end with Trp-Asp (WD). This protein is found in the cytoplasm during interphase, but accumulates at the spindle poles and astral microtubules during mitosis. Reduced expression of this gene results in abnormalities in the size and morphology of the nucleus. Mutations in this gene have been associated with Galloway-Mowat syndrome PMID: 25466283), which is a rare autosomal recessive disorder that affects both the central nervous system and kidneys. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":84639281,"end":84654343,"strand":-1,"description":"WD repeat domain 73 [Source:HGNC Symbol;Acc:HGNC:25928]"}, {"versioned_ensembl_gene_id":"ENSG00000282793.1","gene_symbol":"AC090164.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101527581,"end":101528349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279970.1","gene_symbol":"AC023024.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":101299656,"end":101301648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260342.2","gene_symbol":"AC138811.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18788063,"end":18801519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255092.1","gene_symbol":"AC010768.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44606170,"end":44608101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277210.3","gene_symbol":"AC090164.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101522597,"end":101524739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279062.1","gene_symbol":"CR382287.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10136419,"end":10137004,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115207.13","gene_symbol":"GTF3C2","gene_name":"general transcription factor IIIC subunit 2 [Source:HGNC Symbol;Acc:HGNC:4665]","synonyms":"TFIIIC110,KIAA0011","biotype":"protein_coding","ncbi_id":"2976","summary":null,"start":27325849,"end":27357034,"strand":-1,"description":"general transcription factor IIIC subunit 2 [Source:HGNC Symbol;Acc:HGNC:4665]"}, {"versioned_ensembl_gene_id":"ENSG00000254693.1","gene_symbol":"AC010768.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44604508,"end":44605337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189298.13","gene_symbol":"ZKSCAN3","gene_name":"zinc finger with KRAB and SCAN domains 3 [Source:HGNC Symbol;Acc:HGNC:13853]","synonyms":"Zfp47,ZF47,ZSCAN35,ZNF309,ZNF306","biotype":"protein_coding","ncbi_id":"80317","summary":null,"start":28349914,"end":28369177,"strand":1,"description":"zinc finger with KRAB and SCAN domains 3 [Source:HGNC Symbol;Acc:HGNC:13853]"}, {"versioned_ensembl_gene_id":"ENSG00000273922.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000140479.16","gene_symbol":"PCSK6","gene_name":"proprotein convertase subtilisin/kexin type 6 [Source:HGNC Symbol;Acc:HGNC:8569]","synonyms":"SPC4,PACE4","biotype":"protein_coding","ncbi_id":"5046","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the trans-Golgi network where a second autocatalytic event takes place and the catalytic activity is acquired. The encoded protease is constitutively secreted into the extracellular matrix and expressed in many tissues, including neuroendocrine, liver, gut, and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. Some of its substrates include transforming growth factor beta related proteins, proalbumin, and von Willebrand factor. This gene is thought to play a role in tumor progression and left-right patterning. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Feb 2014]","start":101297142,"end":101525202,"strand":-1,"description":"proprotein convertase subtilisin/kexin type 6 [Source:HGNC Symbol;Acc:HGNC:8569]"}, {"versioned_ensembl_gene_id":"ENSG00000241088.2","gene_symbol":"AC100843.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62415678,"end":62416227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213483.4","gene_symbol":"NDUFAF4P2","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44541]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402676","summary":null,"start":93844789,"end":93845308,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44541]"}, {"versioned_ensembl_gene_id":"ENSG00000260704.1","gene_symbol":"LINC00543","gene_name":"long intergenic non-protein coding RNA 543 [Source:HGNC Symbol;Acc:HGNC:43678]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132234","summary":null,"start":27953526,"end":27955370,"strand":1,"description":"long intergenic non-protein coding RNA 543 [Source:HGNC Symbol;Acc:HGNC:43678]"}, {"versioned_ensembl_gene_id":"ENSG00000276994.1","gene_symbol":"AC245128.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105825.11","gene_symbol":"TFPI2","gene_name":"tissue factor pathway inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:11761]","synonyms":"TFPI-2,REF1,PP5","biotype":"protein_coding","ncbi_id":"7980","summary":"This gene encodes a member of the Kunitz-type serine proteinase inhibitor family. The protein can inhibit a variety of serine proteases including factor VIIa/tissue factor, factor Xa, plasmin, trypsin, chymotryspin and plasma kallikrein. This gene has been identified as a tumor suppressor gene in several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":93885397,"end":93890991,"strand":-1,"description":"tissue factor pathway inhibitor 2 [Source:HGNC Symbol;Acc:HGNC:11761]"}, {"versioned_ensembl_gene_id":"ENSG00000273546.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000158865.12","gene_symbol":"SLC5A11","gene_name":"solute carrier family 5 member 11 [Source:HGNC Symbol;Acc:HGNC:23091]","synonyms":"SMIT2,SGLT6,KST1","biotype":"protein_coding","ncbi_id":"115584","summary":"Cotransporters, such as SLC5A11, represent a major class of proteins that make use of ion gradients to drive active transport for the cellular accumulation of nutrients, neurotransmitters, osmolytes, and ions Roll et al. (2002) [PubMed 12039040].[supplied by OMIM, Mar 2008]","start":24845841,"end":24911628,"strand":1,"description":"solute carrier family 5 member 11 [Source:HGNC Symbol;Acc:HGNC:23091]"}, {"versioned_ensembl_gene_id":"ENSG00000272825.1","gene_symbol":"AL844908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44936303,"end":44936954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165556.9","gene_symbol":"CDX2","gene_name":"caudal type homeobox 2 [Source:HGNC Symbol;Acc:HGNC:1806]","synonyms":"CDX3","biotype":"protein_coding","ncbi_id":"1045","summary":"This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded protein is a major regulator of intestine-specific genes involved in cell growth an differentiation. This protein also plays a role in early embryonic development of the intestinal tract. Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis. [provided by RefSeq, Jan 2012]","start":27962137,"end":27971139,"strand":-1,"description":"caudal type homeobox 2 [Source:HGNC Symbol;Acc:HGNC:1806]"}, {"versioned_ensembl_gene_id":"ENSG00000183250.11","gene_symbol":"LINC01547","gene_name":"long intergenic non-protein coding RNA 1547 [Source:HGNC Symbol;Acc:HGNC:15707]","synonyms":"C21orf67,C21orf69","biotype":"lincRNA","ncbi_id":"84536","summary":null,"start":44932814,"end":44939913,"strand":-1,"description":"long intergenic non-protein coding RNA 1547 [Source:HGNC Symbol;Acc:HGNC:15707]"}, {"versioned_ensembl_gene_id":"ENSG00000273735.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54864204,"end":54872914,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000237758.1","gene_symbol":"BANF1P3","gene_name":"barrier to autointegration factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43883]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505506","summary":null,"start":230725143,"end":230725403,"strand":-1,"description":"barrier to autointegration factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43883]"}, {"versioned_ensembl_gene_id":"ENSG00000233050.1","gene_symbol":"DEFB130B","gene_name":"defensin beta 130B [Source:HGNC Symbol;Acc:HGNC:39814]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100133267","summary":null,"start":12064389,"end":12071747,"strand":-1,"description":"defensin beta 130B [Source:HGNC Symbol;Acc:HGNC:39814]"}, {"versioned_ensembl_gene_id":"ENSG00000178977.3","gene_symbol":"LINC00324","gene_name":"long intergenic non-protein coding RNA 324 [Source:HGNC Symbol;Acc:HGNC:26628]","synonyms":"NCRNA00324,MGC104931,FLJ34790,C17orf44","biotype":"lincRNA","ncbi_id":"284029","summary":null,"start":8220642,"end":8224043,"strand":-1,"description":"long intergenic non-protein coding RNA 324 [Source:HGNC Symbol;Acc:HGNC:26628]"}, {"versioned_ensembl_gene_id":"ENSG00000229859.9","gene_symbol":"PGA3","gene_name":"pepsinogen 3, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8885]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643834","summary":"This gene encodes a protein precursor of the digestive enzyme pepsin, a member of the peptidase A1 family of endopeptidases. The encoded precursor is secreted by gastric chief cells and undergoes autocatalytic cleavage in acidic conditions to form the active enzyme, which functions in the digestion of dietary proteins. This gene is found in a cluster of related genes on chromosome 11, each of which encodes one of multiple pepsinogens. Pepsinogen levels in serum may serve as a biomarker for atrophic gastritis and gastric cancer. [provided by RefSeq, Jul 2015]","start":61203307,"end":61213098,"strand":1,"description":"pepsinogen 3, group I (pepsinogen A) [Source:HGNC Symbol;Acc:HGNC:8885]"}, {"versioned_ensembl_gene_id":"ENSG00000237153.2","gene_symbol":"AL162725.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17018708,"end":17112815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255544.2","gene_symbol":"DEFB108D","gene_name":"defensin beta 108D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26227]","synonyms":"DEFB108P3","biotype":"unprocessed_pseudogene","ncbi_id":"504185","summary":null,"start":12095176,"end":12099536,"strand":-1,"description":"defensin beta 108D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:26227]"}, {"versioned_ensembl_gene_id":"ENSG00000226470.1","gene_symbol":"RPS29P33","gene_name":"ribosomal protein S29 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107987018","summary":null,"start":17096301,"end":17096446,"strand":-1,"description":"ribosomal protein S29 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:52366]"}, {"versioned_ensembl_gene_id":"ENSG00000237729.2","gene_symbol":"AC002075.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93669826,"end":93670077,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237083.1","gene_symbol":"AL162725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17108304,"end":17108604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267487.1","gene_symbol":"AC100843.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62418318,"end":62418576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236607.3","gene_symbol":"EEF1DP8","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51458]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283236","summary":null,"start":62169293,"end":62169828,"strand":1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51458]"}, {"versioned_ensembl_gene_id":"ENSG00000276163.4","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54360692,"end":54377679,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000239533.6","gene_symbol":"GOLGA2P2Y","gene_name":"golgin A2 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:16479]","synonyms":"GOLGA2P2,GOLGA2LY1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"84559","summary":"There are two copies of this pseudogene within the P1 palindrome on chromosome Y. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":24209567,"end":24215581,"strand":-1,"description":"golgin A2 pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:16479]"}, {"versioned_ensembl_gene_id":"ENSG00000256006.1","gene_symbol":"AC084117.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18405609,"end":18406731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235109.7","gene_symbol":"ZSCAN31","gene_name":"zinc finger and SCAN domain containing 31 [Source:HGNC Symbol;Acc:HGNC:14097]","synonyms":"ZNF323,ZNF310P","biotype":"protein_coding","ncbi_id":"64288","summary":"This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":28324693,"end":28356271,"strand":-1,"description":"zinc finger and SCAN domain containing 31 [Source:HGNC Symbol;Acc:HGNC:14097]"}, {"versioned_ensembl_gene_id":"ENSG00000266920.1","gene_symbol":"ACTBP9","gene_name":"actin, beta pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:142]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"69","summary":null,"start":62442028,"end":62443126,"strand":1,"description":"actin, beta pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:142]"}, {"versioned_ensembl_gene_id":"ENSG00000137404.14","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30688047,"end":30691420,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000168515.3","gene_symbol":"SCGB1D1","gene_name":"secretoglobin family 1D member 1 [Source:HGNC Symbol;Acc:HGNC:18395]","synonyms":"LPHA,LIPA,MGC71958","biotype":"protein_coding","ncbi_id":"10648","summary":"The protein encoded by this gene is a member of the lipophilin subfamily, part of the uteroglobin superfamily, and is an ortholog of prostatein, the major secretory glycoprotein of the rat ventral prostate gland. This gene product represents one component of a heterodimeric molecule present in human tears whose elution profile is consistent with prostatein, a tetrameric molecule composed of three peptide components in heterodimers. Assuming that human lipophilins are the functional counterparts of prostatein, they may be transcriptionally regulated by steroid hormones, with the ability to bind androgens, other steroids and possibly bind and concentrate estramustine, a chemotherapeutic agent widely used for prostate cancer. Although the gene has been reported to be on chromosome 15, this sequence appears to be from a cluster of genes on chromosome 11 that includes mammaglobin 2. [provided by RefSeq, Jul 2008]","start":62190216,"end":62193539,"strand":1,"description":"secretoglobin family 1D member 1 [Source:HGNC Symbol;Acc:HGNC:18395]"}, {"versioned_ensembl_gene_id":"ENSG00000272183.1","gene_symbol":"AC005041.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74501717,"end":74502365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257702.3","gene_symbol":"LBX2-AS1","gene_name":"LBX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25136]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"151534","summary":null,"start":74502595,"end":74504678,"strand":1,"description":"LBX2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25136]"}, {"versioned_ensembl_gene_id":"ENSG00000281396.1","gene_symbol":"AL122023.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93334528,"end":93335057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124253.10","gene_symbol":"PCK1","gene_name":"phosphoenolpyruvate carboxykinase 1 [Source:HGNC Symbol;Acc:HGNC:8724]","synonyms":"PEPCK-C","biotype":"protein_coding","ncbi_id":"5105","summary":"This gene is a main control point for the regulation of gluconeogenesis. The cytosolic enzyme encoded by this gene, along with GTP, catalyzes the formation of phosphoenolpyruvate from oxaloacetate, with the release of carbon dioxide and GDP. The expression of this gene can be regulated by insulin, glucocorticoids, glucagon, cAMP, and diet. Defects in this gene are a cause of cytosolic phosphoenolpyruvate carboxykinase deficiency. A mitochondrial isozyme of the encoded protein also has been characterized. [provided by RefSeq, Jul 2008]","start":57561080,"end":57568112,"strand":1,"description":"phosphoenolpyruvate carboxykinase 1 [Source:HGNC Symbol;Acc:HGNC:8724]"}, {"versioned_ensembl_gene_id":"ENSG00000258130.7","gene_symbol":"AC106782.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30204316,"end":30209071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179528.15","gene_symbol":"LBX2","gene_name":"ladybird homeobox 2 [Source:HGNC Symbol;Acc:HGNC:15525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85474","summary":null,"start":74497517,"end":74503316,"strand":-1,"description":"ladybird homeobox 2 [Source:HGNC Symbol;Acc:HGNC:15525]"}, {"versioned_ensembl_gene_id":"ENSG00000259523.1","gene_symbol":"AC022613.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29822631,"end":29824081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234664.1","gene_symbol":"HMGN2P5","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33568]","synonyms":"HMGN2L5","biotype":"processed_pseudogene","ncbi_id":"727795","summary":null,"start":29730713,"end":29730985,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33568]"}, {"versioned_ensembl_gene_id":"ENSG00000169813.16","gene_symbol":"HNRNPF","gene_name":"heterogeneous nuclear ribonucleoprotein F [Source:HGNC Symbol;Acc:HGNC:5039]","synonyms":"HNRPF","biotype":"protein_coding","ncbi_id":"3185","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing, polyadenylation, and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNAs which have guanosine-rich sequences. This protein is very similar to the family member hnRPH. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":43385617,"end":43409166,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein F [Source:HGNC Symbol;Acc:HGNC:5039]"}, {"versioned_ensembl_gene_id":"ENSG00000236677.1","gene_symbol":"AP000688.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36060432,"end":36064408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230212.6","gene_symbol":"AP000688.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36069642,"end":36126640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122778.9","gene_symbol":"KIAA1549","gene_name":"KIAA1549 [Source:HGNC Symbol;Acc:HGNC:22219]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57670","summary":"The protein encoded by this gene belongs to the UPF0606 family. This gene has been found to be fused to the BRAF oncogene in many cases of pilocytic astrocytoma. The fusion results from 2Mb tandem duplications at 7q34. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]","start":138831381,"end":138981318,"strand":-1,"description":"KIAA1549 [Source:HGNC Symbol;Acc:HGNC:22219]"}, {"versioned_ensembl_gene_id":"ENSG00000272644.1","gene_symbol":"AC097468.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219069354,"end":219069809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159228.12","gene_symbol":"CBR1","gene_name":"carbonyl reductase 1 [Source:HGNC Symbol;Acc:HGNC:1548]","synonyms":"SDR21C1,CBR","biotype":"protein_coding","ncbi_id":"873","summary":"The protein encoded by this gene belongs to the short-chain dehydrogenases/reductases (SDR) family, which function as NADPH-dependent oxidoreductases having wide specificity for carbonyl compounds, such as quinones, prostaglandins, and various xenobiotics. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2013]","start":36069941,"end":36073166,"strand":1,"description":"carbonyl reductase 1 [Source:HGNC Symbol;Acc:HGNC:1548]"}, {"versioned_ensembl_gene_id":"ENSG00000278887.1","gene_symbol":"AC106782.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30206510,"end":30206927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276416.3","gene_symbol":"UNC79","gene_name":"unc-79 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:19966]","synonyms":"KIAA1409","biotype":"protein_coding","ncbi_id":"57578","summary":"The NALCN channel is responsible for Na(+) leak currents. The protein encoded by this gene, along with UNC80, is an accessory subunit of the NALCN channel that contributes to the Ca(2+) sensitivity of the channel. [provided by RefSeq, Sep 2016]","start":93333219,"end":93707876,"strand":1,"description":"unc-79 homolog, NALCN channel complex subunit [Source:HGNC Symbol;Acc:HGNC:19966]"}, {"versioned_ensembl_gene_id":"ENSG00000261052.5","gene_symbol":"SULT1A3","gene_name":"sulfotransferase family 1A member 3 [Source:HGNC Symbol;Acc:HGNC:11455]","synonyms":"STM,TL-PST","biotype":"protein_coding","ncbi_id":"6818","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a phenol sulfotransferase with thermolabile enzyme activity. Four sulfotransferase genes are located on the p arm of chromosome 16; this gene and SULT1A4 arose from a segmental duplication. This gene is the most centromeric of the four sulfotransferase genes. Read-through transcription exists between this gene and the upstream SLX1A (SLX1 structure-specific endonuclease subunit homolog A) gene that encodes a protein containing GIY-YIG domains. [provided by RefSeq, Nov 2010]","start":30199228,"end":30204310,"strand":1,"description":"sulfotransferase family 1A member 3 [Source:HGNC Symbol;Acc:HGNC:11455]"}, {"versioned_ensembl_gene_id":"ENSG00000279682.1","gene_symbol":"AC120338.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7489659,"end":7491199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278388.1","gene_symbol":"AC002076.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":93914987,"end":93915108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141098.12","gene_symbol":"GFOD2","gene_name":"glucose-fructose oxidoreductase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28159]","synonyms":"MGC11335,FLJ23802","biotype":"protein_coding","ncbi_id":"81577","summary":null,"start":67674531,"end":67719421,"strand":-1,"description":"glucose-fructose oxidoreductase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28159]"}, {"versioned_ensembl_gene_id":"ENSG00000215914.4","gene_symbol":"MMP23A","gene_name":"matrix metallopeptidase 23A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7170]","synonyms":"MMP21,MIFR","biotype":"unprocessed_pseudogene","ncbi_id":"8511","summary":"This locus represents the partially duplicated copy of the MMP23B gene, and therefore considered a pseudogene. This pseudogene is part of a duplicated region of chromosome 1p36.3. It belongs to the more centromeric copy of the duplicated region. [provided by RefSeq, Jul 2008]","start":1699942,"end":1701782,"strand":1,"description":"matrix metallopeptidase 23A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7170]"}, {"versioned_ensembl_gene_id":"ENSG00000279656.1","gene_symbol":"AL132780.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23023083,"end":23024217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099904.15","gene_symbol":"ZDHHC8","gene_name":"zinc finger DHHC-type containing 8 [Source:HGNC Symbol;Acc:HGNC:18474]","synonyms":"ZNF378,KIAA1292","biotype":"protein_coding","ncbi_id":"29801","summary":"This gene encodes a four transmembrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein may function as a palmitoyltransferase. Defects in this gene may be associated with a susceptibility to schizophrenia. Alternate splicing of this gene results in multiple transcript variants. A pseudogene of this gene is found on chromosome 22.[provided by RefSeq, May 2010]","start":20129456,"end":20148007,"strand":1,"description":"zinc finger DHHC-type containing 8 [Source:HGNC Symbol;Acc:HGNC:18474]"}, {"versioned_ensembl_gene_id":"ENSG00000100804.18","gene_symbol":"PSMB5","gene_name":"proteasome subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:9542]","synonyms":"X,MB1","biotype":"protein_coding","ncbi_id":"5693","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit in the proteasome. This catalytic subunit is not present in the immunoproteasome and is replaced by catalytic subunit 3i (proteasome beta 8 subunit). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":23016543,"end":23035230,"strand":-1,"description":"proteasome subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:9542]"}, {"versioned_ensembl_gene_id":"ENSG00000147130.14","gene_symbol":"ZMYM3","gene_name":"zinc finger MYM-type containing 3 [Source:HGNC Symbol;Acc:HGNC:13054]","synonyms":"ZNF198L2,MYM,KIAA0385,DXS6673E,ZNF261","biotype":"protein_coding","ncbi_id":"9203","summary":"This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010]","start":71239624,"end":71255146,"strand":-1,"description":"zinc finger MYM-type containing 3 [Source:HGNC Symbol;Acc:HGNC:13054]"}, {"versioned_ensembl_gene_id":"ENSG00000265564.1","gene_symbol":"PIGPP4","gene_name":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45156]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480811","summary":null,"start":9880580,"end":9880886,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45156]"}, {"versioned_ensembl_gene_id":"ENSG00000116990.10","gene_symbol":"MYCL","gene_name":"MYCL proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7555]","synonyms":"bHLHe38,MYCL1,LMYC","biotype":"protein_coding","ncbi_id":"4610","summary":null,"start":39895426,"end":39902256,"strand":-1,"description":"MYCL proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7555]"}, {"versioned_ensembl_gene_id":"ENSG00000281627.1","gene_symbol":"DUX4L3","gene_name":"double homeobox 4 like 3 [Source:HGNC Symbol;Acc:HGNC:38688]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653548","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190087705,"end":190088979,"strand":1,"description":"double homeobox 4 like 3 [Source:HGNC Symbol;Acc:HGNC:38688]"}, {"versioned_ensembl_gene_id":"ENSG00000280096.1","gene_symbol":"AC015967.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35082009,"end":35082242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166974.12","gene_symbol":"MAPRE2","gene_name":"microtubule associated protein RP/EB family member 2 [Source:HGNC Symbol;Acc:HGNC:6891]","synonyms":"EB1,RP1,EB2","biotype":"protein_coding","ncbi_id":"10982","summary":"The protein encoded by this gene shares significant homology to the adenomatous polyposis coli (APC) protein-binding EB1 gene family. This protein is a microtubule-associated protein that is necessary for spindle symmetry during mitosis. It is thought to play a role in the tumorigenesis of colorectal cancers and the proliferative control of normal cells. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":34976928,"end":35143470,"strand":1,"description":"microtubule associated protein RP/EB family member 2 [Source:HGNC Symbol;Acc:HGNC:6891]"}, {"versioned_ensembl_gene_id":"ENSG00000280457.1","gene_symbol":"DUX4L2","gene_name":"double homeobox 4 like 2 [Source:HGNC Symbol;Acc:HGNC:37267]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728410","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190091005,"end":190092279,"strand":1,"description":"double homeobox 4 like 2 [Source:HGNC Symbol;Acc:HGNC:37267]"}, {"versioned_ensembl_gene_id":"ENSG00000145592.13","gene_symbol":"RPL37","gene_name":"ribosomal protein L37 [Source:HGNC Symbol;Acc:HGNC:10347]","synonyms":"L37","biotype":"protein_coding","ncbi_id":"6167","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L37E family of ribosomal proteins. It is located in the cytoplasm. The protein contains a C2C2-type zinc finger-like motif. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":40825262,"end":40835335,"strand":-1,"description":"ribosomal protein L37 [Source:HGNC Symbol;Acc:HGNC:10347]"}, {"versioned_ensembl_gene_id":"ENSG00000223443.2","gene_symbol":"USP17L2","gene_name":"ubiquitin specific peptidase 17-like family member 2 [Source:HGNC Symbol;Acc:HGNC:34434]","synonyms":"DUB3","biotype":"protein_coding","ncbi_id":"377630","summary":"DUB3 is a member of the ubiquitin processing protease (UBP) subfamily of deubiquitinating enzymes. See USP1 (MIM 603478) for background information.[supplied by OMIM, Mar 2008]","start":12137168,"end":12139077,"strand":-1,"description":"ubiquitin specific peptidase 17-like family member 2 [Source:HGNC Symbol;Acc:HGNC:34434]"}, {"versioned_ensembl_gene_id":"ENSG00000276007.1","gene_symbol":"AC079414.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":78123243,"end":78124332,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260479.1","gene_symbol":"AC009145.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79090050,"end":79101754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277954.1","gene_symbol":"AC092376.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79202624,"end":79206739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134775.15","gene_symbol":"FHOD3","gene_name":"formin homology 2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26178]","synonyms":"KIAA1695,FLJ22717,FLJ22297,FHOS2","biotype":"protein_coding","ncbi_id":"80206","summary":"The protein encoded by this gene is a member of the diaphanous-related formins (DRF), and contains multiple domains, including GBD (GTPase-binding domain), DID (diaphanous inhibitory domain), FH1 (formin homology 1), FH2 (formin homology 2), and DAD (diaphanous auto-regulatory domain) domains. This protein is thought to play a role in actin filament polymerization in cardiomyocytes. Mutations in this gene have been associated with dilated cardiomyopathy (DCM), characterized by dilation of the ventricular chamber, leading to impairment of systolic pump function and subsequent heart failure. Increased levels of the protein encoded by this gene have been observed in individuals with hypertrophic cardiomyopathy (HCM). Alternative splicing results in multiple transcript variants encoding different isoforms. A muscle-specific isoform has been shown to possess a casein kinase 2 (CK2) phosphorylation site at the C-terminal end of the FH2 domain. Phosphorylation of this site alters its interaction with sequestosome 1 (SQSTM1), and targets this isoform to myofibrils, while other isoforms form cytoplasmic aggregates. [provided by RefSeq, Aug 2015]","start":36297714,"end":36780055,"strand":1,"description":"formin homology 2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26178]"}, {"versioned_ensembl_gene_id":"ENSG00000236546.1","gene_symbol":"AL033527.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39897745,"end":39899098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261512.2","gene_symbol":"AC092368.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46622861,"end":46624451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279129.1","gene_symbol":"AC046158.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78550739,"end":78553296,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109743.10","gene_symbol":"BST1","gene_name":"bone marrow stromal cell antigen 1 [Source:HGNC Symbol;Acc:HGNC:1118]","synonyms":"CD157","biotype":"protein_coding","ncbi_id":"683","summary":"Bone marrow stromal cell antigen-1 is a stromal cell line-derived glycosylphosphatidylinositol-anchored molecule that facilitates pre-B-cell growth. The deduced amino acid sequence exhibits 33% similarity with CD38. BST1 expression is enhanced in bone marrow stromal cell lines derived from patients with rheumatoid arthritis. The polyclonal B-cell abnormalities in rheumatoid arthritis may be, at least in part, attributed to BST1 overexpression in the stromal cell population. [provided by RefSeq, Jul 2008]","start":15702950,"end":15738313,"strand":1,"description":"bone marrow stromal cell antigen 1 [Source:HGNC Symbol;Acc:HGNC:1118]"}, {"versioned_ensembl_gene_id":"ENSG00000282850.2","gene_symbol":"RHOXF1P2","gene_name":"Rhox homeobox family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51611]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075106","summary":null,"start":119998087,"end":120000088,"strand":-1,"description":"Rhox homeobox family member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51611]"}, {"versioned_ensembl_gene_id":"ENSG00000279991.1","gene_symbol":"AC009044.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78166717,"end":78168514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226430.6","gene_symbol":"USP17L7","gene_name":"ubiquitin specific peptidase 17-like family member 7 [Source:HGNC Symbol;Acc:HGNC:37180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392197","summary":null,"start":12132417,"end":12134438,"strand":-1,"description":"ubiquitin specific peptidase 17-like family member 7 [Source:HGNC Symbol;Acc:HGNC:37180]"}, {"versioned_ensembl_gene_id":"ENSG00000260816.2","gene_symbol":"AC027279.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":78895361,"end":78899644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144681.10","gene_symbol":"STAC","gene_name":"SH3 and cysteine rich domain [Source:HGNC Symbol;Acc:HGNC:11353]","synonyms":"STAC1","biotype":"protein_coding","ncbi_id":"6769","summary":null,"start":36380344,"end":36548007,"strand":1,"description":"SH3 and cysteine rich domain [Source:HGNC Symbol;Acc:HGNC:11353]"}, {"versioned_ensembl_gene_id":"ENSG00000260694.1","gene_symbol":"AC009145.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79077376,"end":79078234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253799.1","gene_symbol":"LINC01030","gene_name":"long intergenic non-protein coding RNA 1030 [Source:HGNC Symbol;Acc:HGNC:49016]","synonyms":"TCONS_00015085","biotype":"lincRNA","ncbi_id":"101937451","summary":null,"start":90592804,"end":90606065,"strand":-1,"description":"long intergenic non-protein coding RNA 1030 [Source:HGNC Symbol;Acc:HGNC:49016]"}, {"versioned_ensembl_gene_id":"ENSG00000279732.1","gene_symbol":"AC027279.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78981722,"end":78981843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105784.15","gene_symbol":"RUNDC3B","gene_name":"RUN domain containing 3B [Source:HGNC Symbol;Acc:HGNC:30286]","synonyms":"RPIP9,RPIB9","biotype":"protein_coding","ncbi_id":"154661","summary":null,"start":87627548,"end":87832296,"strand":1,"description":"RUN domain containing 3B [Source:HGNC Symbol;Acc:HGNC:30286]"}, {"versioned_ensembl_gene_id":"ENSG00000135932.10","gene_symbol":"CAB39","gene_name":"calcium binding protein 39 [Source:HGNC Symbol;Acc:HGNC:20292]","synonyms":"MO25,CGI-66","biotype":"protein_coding","ncbi_id":"51719","summary":null,"start":230712845,"end":230821075,"strand":1,"description":"calcium binding protein 39 [Source:HGNC Symbol;Acc:HGNC:20292]"}, {"versioned_ensembl_gene_id":"ENSG00000254455.1","gene_symbol":"HIGD1AP10","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:43005]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287960","summary":null,"start":65145691,"end":65145972,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:43005]"}, {"versioned_ensembl_gene_id":"ENSG00000281979.1","gene_symbol":"AC216130.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":103164581,"end":103165294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133789.14","gene_symbol":"SWAP70","gene_name":"SWAP switching B-cell complex subunit 70 [Source:HGNC Symbol;Acc:HGNC:17070]","synonyms":"SWAP-70,KIAA0640","biotype":"protein_coding","ncbi_id":"23075","summary":null,"start":9664077,"end":9752991,"strand":1,"description":"SWAP switching B-cell complex subunit 70 [Source:HGNC Symbol;Acc:HGNC:17070]"}, {"versioned_ensembl_gene_id":"ENSG00000065911.11","gene_symbol":"MTHFD2","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase [Source:HGNC Symbol;Acc:HGNC:7434]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10797","summary":"This gene encodes a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. Alternative splicing results in two different transcripts, one protein-coding and the other not protein-coding. This gene has a pseudogene on chromosome 7. [provided by RefSeq, Mar 2009]","start":74198562,"end":74217565,"strand":1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase [Source:HGNC Symbol;Acc:HGNC:7434]"}, {"versioned_ensembl_gene_id":"ENSG00000243305.1","gene_symbol":"AC026347.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152457759,"end":152496813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131355.14","gene_symbol":"ADGRE3","gene_name":"adhesion G protein-coupled receptor E3 [Source:HGNC Symbol;Acc:HGNC:23647]","synonyms":"EMR3","biotype":"protein_coding","ncbi_id":"84658","summary":"This gene encodes a member of the class B seven-span transmembrane (TM7) receptor family expressed predominantly by cells of the immune system. Family members are characterized by an extended extracellular region with a variable number of N-terminal epidermal growth factor (EGF)-like domains coupled to a TM7 domain via a mucin-like spacer domain. This gene is closely linked to the gene encoding egf-like molecule containing mucin-like hormone receptor 2 on chromosome 19. This protein may play a role in myeloid-myeloid interactions during immune and inflammatory responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2014]","start":14619117,"end":14690027,"strand":-1,"description":"adhesion G protein-coupled receptor E3 [Source:HGNC Symbol;Acc:HGNC:23647]"}, {"versioned_ensembl_gene_id":"ENSG00000163705.12","gene_symbol":"FANCD2OS","gene_name":"FANCD2 opposite strand [Source:HGNC Symbol;Acc:HGNC:28623]","synonyms":"MGC40179,C3orf24","biotype":"protein_coding","ncbi_id":"115795","summary":"This gene encodes a conserved protein of unknown function. [provided by RefSeq, Jan 2013]","start":10081317,"end":10108231,"strand":-1,"description":"FANCD2 opposite strand [Source:HGNC Symbol;Acc:HGNC:28623]"}, {"versioned_ensembl_gene_id":"ENSG00000234173.1","gene_symbol":"AL353784.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54486230,"end":54656051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215183.4","gene_symbol":"MSMP","gene_name":"microseminoprotein, prostate associated [Source:HGNC Symbol;Acc:HGNC:29663]","synonyms":"PSMP,PC-3","biotype":"protein_coding","ncbi_id":"692094","summary":"This gene encodes a member of the beta-microseminoprotein family. Members of this protein family contain ten conserved cysteine residues that form intra-molecular disulfide bonds. The encoded protein may play a role in prostate cancer tumorigenesis. [provided by RefSeq, Jan 2011]","start":35752990,"end":35756613,"strand":-1,"description":"microseminoprotein, prostate associated [Source:HGNC Symbol;Acc:HGNC:29663]"}, {"versioned_ensembl_gene_id":"ENSG00000219592.2","gene_symbol":"NCSTNP1","gene_name":"nicastrin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39606]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873743","summary":null,"start":27492118,"end":27492261,"strand":1,"description":"nicastrin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39606]"}, {"versioned_ensembl_gene_id":"ENSG00000229217.1","gene_symbol":"CYCSP11","gene_name":"cytochrome c, somatic pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:24385]","synonyms":"HCP11","biotype":"processed_pseudogene","ncbi_id":"360167","summary":null,"start":10057973,"end":10058287,"strand":-1,"description":"cytochrome c, somatic pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:24385]"}, {"versioned_ensembl_gene_id":"ENSG00000164010.13","gene_symbol":"ERMAP","gene_name":"erythroblast membrane associated protein (Scianna blood group) [Source:HGNC Symbol;Acc:HGNC:15743]","synonyms":"SC,RD,BTN5","biotype":"protein_coding","ncbi_id":"114625","summary":"The protein encoded by this gene is a cell surface transmembrane protein that may act as an erythroid cell receptor, possibly as a mediator of cell adhesion. Polymorphisms in this gene are responsible for the Scianna/Radin blood group system. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":42817124,"end":42844989,"strand":1,"description":"erythroblast membrane associated protein (Scianna blood group) [Source:HGNC Symbol;Acc:HGNC:15743]"}, {"versioned_ensembl_gene_id":"ENSG00000224819.1","gene_symbol":"AC093843.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":220791078,"end":220797893,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183347.14","gene_symbol":"GBP6","gene_name":"guanylate binding protein family member 6 [Source:HGNC Symbol;Acc:HGNC:25395]","synonyms":"DKFZp686G0786","biotype":"protein_coding","ncbi_id":"163351","summary":"Guanylate-binding proteins, such as GBP6, are induced by interferon and hydrolyze GTP to both GDP and GMP (Olszewski et al., 2006 [PubMed 16689661]).[supplied by OMIM, Dec 2008]","start":89364058,"end":89386461,"strand":1,"description":"guanylate binding protein family member 6 [Source:HGNC Symbol;Acc:HGNC:25395]"}, {"versioned_ensembl_gene_id":"ENSG00000233235.1","gene_symbol":"BX119321.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89324522,"end":89334880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005471.15","gene_symbol":"ABCB4","gene_name":"ATP binding cassette subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:45]","synonyms":"MDR2,GBD1,PGY3,PFIC-3,MDR3","biotype":"protein_coding","ncbi_id":"5244","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a full transporter and member of the p-glycoprotein family of membrane proteins with phosphatidylcholine as its substrate. The function of this protein has not yet been determined; however, it may involve transport of phospholipids from liver hepatocytes into bile. Alternative splicing of this gene results in several products of undetermined function. [provided by RefSeq, Jul 2008]","start":87401697,"end":87480435,"strand":-1,"description":"ATP binding cassette subfamily B member 4 [Source:HGNC Symbol;Acc:HGNC:45]"}, {"versioned_ensembl_gene_id":"ENSG00000255463.1","gene_symbol":"AC011979.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9631008,"end":9631359,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000003989.17","gene_symbol":"SLC7A2","gene_name":"solute carrier family 7 member 2 [Source:HGNC Symbol;Acc:HGNC:11060]","synonyms":"HCAT2,CAT-2,ATRC2","biotype":"protein_coding","ncbi_id":"6542","summary":"The protein encoded by this gene is a cationic amino acid transporter and a member of the APC (amino acid-polyamine-organocation) family of transporters. The encoded membrane protein is responsible for the cellular uptake of arginine, lysine and ornithine. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":17497088,"end":17570573,"strand":1,"description":"solute carrier family 7 member 2 [Source:HGNC Symbol;Acc:HGNC:11060]"}, {"versioned_ensembl_gene_id":"ENSG00000120798.16","gene_symbol":"NR2C1","gene_name":"nuclear receptor subfamily 2 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7971]","synonyms":"TR2-11,TR2","biotype":"protein_coding","ncbi_id":"7181","summary":"This gene encodes a nuclear hormone receptor characterized by a highly conserved DNA binding domain (DBD), a variable hinge region, and a carboxy-terminal ligand binding domain (LBD) that is typical for all members of the steroid/thyroid hormone receptor superfamily. This protein also belongs to a large family of ligand-inducible transcription factors that regulate gene expression by binding to specific DNA sequences within promoters of target genes. Multiple alternatively spliced transcript variants have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":95020229,"end":95073703,"strand":-1,"description":"nuclear receptor subfamily 2 group C member 1 [Source:HGNC Symbol;Acc:HGNC:7971]"}, {"versioned_ensembl_gene_id":"ENSG00000235241.1","gene_symbol":"BX284668.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16889095,"end":16889602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230239.1","gene_symbol":"BX284668.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16855407,"end":16859284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138771.14","gene_symbol":"SHROOM3","gene_name":"shroom family member 3 [Source:HGNC Symbol;Acc:HGNC:30422]","synonyms":"ShrmL,SHRM,KIAA1481,APXL3","biotype":"protein_coding","ncbi_id":"57619","summary":"This gene encodes a PDZ-domain-containing protein that belongs to a family of Shroom-related proteins. This protein may be involved in regulating cell shape in certain tissues. A similar protein in mice is required for proper neurulation. [provided by RefSeq, Jan 2011]","start":76435100,"end":76783253,"strand":1,"description":"shroom family member 3 [Source:HGNC Symbol;Acc:HGNC:30422]"}, {"versioned_ensembl_gene_id":"ENSG00000130377.13","gene_symbol":"ACSBG2","gene_name":"acyl-CoA synthetase bubblegum family member 2 [Source:HGNC Symbol;Acc:HGNC:24174]","synonyms":"PRTD-NY3,DKFZp434K1635,BGR","biotype":"protein_coding","ncbi_id":"81616","summary":null,"start":6135247,"end":6193094,"strand":1,"description":"acyl-CoA synthetase bubblegum family member 2 [Source:HGNC Symbol;Acc:HGNC:24174]"}, {"versioned_ensembl_gene_id":"ENSG00000275047.1","gene_symbol":"GU182355.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54830927,"end":54845947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146049.1","gene_symbol":"KAAG1","gene_name":"kidney associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:21031]","synonyms":"RU2AS,RU2","biotype":"protein_coding","ncbi_id":"353219","summary":null,"start":24356903,"end":24358284,"strand":1,"description":"kidney associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:21031]"}, {"versioned_ensembl_gene_id":"ENSG00000186471.12","gene_symbol":"AKAP14","gene_name":"A-kinase anchoring protein 14 [Source:HGNC Symbol;Acc:HGNC:24061]","synonyms":"AKAP28","biotype":"protein_coding","ncbi_id":"158798","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The protein anchors PKA in ciliary axonemes and, in this way, may play a role in regulating ciliary beat frequency. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":119895837,"end":119920716,"strand":1,"description":"A-kinase anchoring protein 14 [Source:HGNC Symbol;Acc:HGNC:24061]"}, {"versioned_ensembl_gene_id":"ENSG00000268455.1","gene_symbol":"AC073544.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23596122,"end":23598159,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168002.11","gene_symbol":"POLR2G","gene_name":"RNA polymerase II subunit G [Source:HGNC Symbol;Acc:HGNC:9194]","synonyms":"RPB7,hsRPB7,hRPB19","biotype":"protein_coding","ncbi_id":"5436","summary":"This gene encodes the seventh largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The protein functions in transcription initiation, and is also thought to help stabilize transcribing polyermase molecules during elongation. [provided by RefSeq, Jan 2009]","start":62761544,"end":62766710,"strand":1,"description":"RNA polymerase II subunit G [Source:HGNC Symbol;Acc:HGNC:9194]"}, {"versioned_ensembl_gene_id":"ENSG00000163159.12","gene_symbol":"VPS72","gene_name":"vacuolar protein sorting 72 homolog [Source:HGNC Symbol;Acc:HGNC:11644]","synonyms":"YL1,YL-1,TCFL1,Swc2","biotype":"protein_coding","ncbi_id":"6944","summary":"The protein encoded by this gene is a shared subunit of two multi-component complexes, the histone acetyltransferase complex TRRAP/TIP60 as well as the chromatin remodeling SRCAP-containing complex. The TRRAP/TIP60 complex acetylates nucleosomal histones important for transcriptional regulation, double strand DNA break repair and apoptosis. The SRCAP-containing complex catalyzes the exchange of histone H2A with the histone variant Htz1 (H2AFZ) into nucleosomes. This protein may be responsible for binding H2AFZ, which has a role in chromosome segregation. This protein may also have a role in regulating long-term hematopoietic stem cell activity. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":151169987,"end":151195321,"strand":-1,"description":"vacuolar protein sorting 72 homolog [Source:HGNC Symbol;Acc:HGNC:11644]"}, {"versioned_ensembl_gene_id":"ENSG00000237914.5","gene_symbol":"SIRPG-AS1","gene_name":"SIRPG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51229]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929010","summary":null,"start":1633508,"end":1648472,"strand":1,"description":"SIRPG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51229]"}, {"versioned_ensembl_gene_id":"ENSG00000231439.4","gene_symbol":"WASIR2","gene_name":"WASH and IL9R antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:38609]","synonyms":"NCRNA00286A","biotype":"lincRNA","ncbi_id":"100132169","summary":null,"start":22910,"end":25123,"strand":1,"description":"WASH and IL9R antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:38609]"}, {"versioned_ensembl_gene_id":"ENSG00000189136.8","gene_symbol":"UBE2Q2P1","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37439]","synonyms":"UBE2QP1,FLJ43276","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"388165","summary":null,"start":84526781,"end":84571216,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37439]"}, {"versioned_ensembl_gene_id":"ENSG00000178602.7","gene_symbol":"OTOS","gene_name":"otospiralin [Source:HGNC Symbol;Acc:HGNC:22644]","synonyms":"OTOSP","biotype":"protein_coding","ncbi_id":"150677","summary":"Otospiralin is synthesized by nonsensory cells (fibrocytes) of the inner ear, and downregulation of otospiralin in guinea pigs leads to deafness (Lavigne-Rebillard et al., 2003 [PubMed 12687421]).[supplied by OMIM, Mar 2008]","start":240139026,"end":240144562,"strand":-1,"description":"otospiralin [Source:HGNC Symbol;Acc:HGNC:22644]"}, {"versioned_ensembl_gene_id":"ENSG00000167702.11","gene_symbol":"KIFC2","gene_name":"kinesin family member C2 [Source:HGNC Symbol;Acc:HGNC:29530]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90990","summary":null,"start":144466043,"end":144474202,"strand":1,"description":"kinesin family member C2 [Source:HGNC Symbol;Acc:HGNC:29530]"}, {"versioned_ensembl_gene_id":"ENSG00000179277.9","gene_symbol":"MEIS3P1","gene_name":"Meis homeobox 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7002]","synonyms":"MRG2,MEIS4,MEIS3","biotype":"processed_pseudogene","ncbi_id":"4213","summary":"This gene appears to be a retrotransposed pseudogene based on its lack of exons compared to other family members, one of which is found on chromosome 19 (MEIS3). It does appear to be transcribed and has an ORF that may encode a protein of similar size and sequence to that encoded by MEIS3. [provided by RefSeq, Jul 2008]","start":15786618,"end":15787575,"strand":1,"description":"Meis homeobox 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7002]"}, {"versioned_ensembl_gene_id":"ENSG00000270670.1","gene_symbol":"MARK2P16","gene_name":"microtubule affinity regulating kinase 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45171]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533795","summary":null,"start":89837612,"end":89839334,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:45171]"}, {"versioned_ensembl_gene_id":"ENSG00000260251.1","gene_symbol":"AC092368.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46573763,"end":46575094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232229.5","gene_symbol":"LINC00865","gene_name":"long intergenic non-protein coding RNA 865 [Source:HGNC Symbol;Acc:HGNC:45170]","synonyms":null,"biotype":"lincRNA","ncbi_id":"643529","summary":null,"start":89829510,"end":89840861,"strand":1,"description":"long intergenic non-protein coding RNA 865 [Source:HGNC Symbol;Acc:HGNC:45170]"}, {"versioned_ensembl_gene_id":"ENSG00000075673.11","gene_symbol":"ATP12A","gene_name":"ATPase H+/K+ transporting non-gastric alpha2 subunit [Source:HGNC Symbol;Acc:HGNC:13816]","synonyms":"HK,ATP1AL1,2,#945","biotype":"protein_coding","ncbi_id":"479","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This gene encodes a catalytic subunit of the ouabain-sensitive H+/K+ -ATPase that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for potassium absorption in various tissues. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":24680411,"end":24712493,"strand":1,"description":"ATPase H+/K+ transporting non-gastric alpha2 subunit [Source:HGNC Symbol;Acc:HGNC:13816]"}, {"versioned_ensembl_gene_id":"ENSG00000277957.1","gene_symbol":"SENP3-EIF4A1","gene_name":"SENP3-EIF4A1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49182]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533955","summary":"This locus represents naturally occurring read-through transcription between the neighboring SUMO1/sentrin/SMT3 specific peptidase 3 (SENP3) and eukaryotic translation initiation factor 4A1 (EIF4A1) genes on chromosome 17. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":7563287,"end":7578715,"strand":1,"description":"SENP3-EIF4A1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49182]"}, {"versioned_ensembl_gene_id":"ENSG00000272887.1","gene_symbol":"CSPG4P5","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29403]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"114817","summary":null,"start":84401807,"end":84408005,"strand":-1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:29403]"}, {"versioned_ensembl_gene_id":"ENSG00000271360.1","gene_symbol":"AL512631.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11611305,"end":11612227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235108.1","gene_symbol":"IFNA12P","gene_name":"interferon alpha 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:5443]","synonyms":"IFNP12","biotype":"unprocessed_pseudogene","ncbi_id":"158011","summary":null,"start":21403081,"end":21403651,"strand":1,"description":"interferon alpha 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:5443]"}, {"versioned_ensembl_gene_id":"ENSG00000182872.15","gene_symbol":"RBM10","gene_name":"RNA binding motif protein 10 [Source:HGNC Symbol;Acc:HGNC:9896]","synonyms":"ZRANB5,KIAA0122,GPATCH9,GPATC9,DXS8237E","biotype":"protein_coding","ncbi_id":"8241","summary":"This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]","start":47144869,"end":47186813,"strand":1,"description":"RNA binding motif protein 10 [Source:HGNC Symbol;Acc:HGNC:9896]"}, {"versioned_ensembl_gene_id":"ENSG00000154736.5","gene_symbol":"ADAMTS5","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 5 [Source:HGNC Symbol;Acc:HGNC:221]","synonyms":"ADMP-2,ADAMTS11","biotype":"protein_coding","ncbi_id":"11096","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme contains two C-terminal TS motifs and functions as an aggrecanase that cleaves aggrecan, a major proteoglycan of cartilage, and may mediate cartilage destruction in osteoarthritis. [provided by RefSeq, Feb 2016]","start":26917912,"end":26966513,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 5 [Source:HGNC Symbol;Acc:HGNC:221]"}, {"versioned_ensembl_gene_id":"ENSG00000150054.18","gene_symbol":"MPP7","gene_name":"membrane palmitoylated protein 7 [Source:HGNC Symbol;Acc:HGNC:26542]","synonyms":"FLJ32798","biotype":"protein_coding","ncbi_id":"143098","summary":"The protein encoded by this gene is a member of the p55 Stardust family of membrane-associated guanylate kinase (MAGUK) proteins, which function in the establishment of epithelial cell polarity. This family member forms a complex with the polarity protein DLG1 (discs, large homolog 1) and facilitates epithelial cell polarity and tight junction formation. Polymorphisms in this gene are associated with variations in site-specific bone mineral density (BMD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":28050993,"end":28334486,"strand":-1,"description":"membrane palmitoylated protein 7 [Source:HGNC Symbol;Acc:HGNC:26542]"}, {"versioned_ensembl_gene_id":"ENSG00000277585.5","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195746765,"end":195819600,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000196569.11","gene_symbol":"LAMA2","gene_name":"laminin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6482]","synonyms":"LAMM","biotype":"protein_coding","ncbi_id":"3908","summary":"Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008]","start":128883141,"end":129516569,"strand":1,"description":"laminin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6482]"}, {"versioned_ensembl_gene_id":"ENSG00000233351.1","gene_symbol":"AL356124.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129479615,"end":129481410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162383.11","gene_symbol":"SLC1A7","gene_name":"solute carrier family 1 member 7 [Source:HGNC Symbol;Acc:HGNC:10945]","synonyms":"EAAT5","biotype":"protein_coding","ncbi_id":"6512","summary":null,"start":53087179,"end":53142632,"strand":-1,"description":"solute carrier family 1 member 7 [Source:HGNC Symbol;Acc:HGNC:10945]"}, {"versioned_ensembl_gene_id":"ENSG00000260550.2","gene_symbol":"AC136618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18570448,"end":18571683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231252.2","gene_symbol":"AC099792.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60659631,"end":60867998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228116.9","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32129213,"end":32134104,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000164465.18","gene_symbol":"DCBLD1","gene_name":"discoidin, CUB and LCCL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21479]","synonyms":"MGC46341,dJ94G16.1","biotype":"protein_coding","ncbi_id":"285761","summary":null,"start":117453817,"end":117569858,"strand":1,"description":"discoidin, CUB and LCCL domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21479]"}, {"versioned_ensembl_gene_id":"ENSG00000120235.4","gene_symbol":"IFNA6","gene_name":"interferon alpha 6 [Source:HGNC Symbol;Acc:HGNC:5427]","synonyms":"IFN-alphaK","biotype":"protein_coding","ncbi_id":"3443","summary":null,"start":21349835,"end":21351378,"strand":-1,"description":"interferon alpha 6 [Source:HGNC Symbol;Acc:HGNC:5427]"}, {"versioned_ensembl_gene_id":"ENSG00000160746.12","gene_symbol":"ANO10","gene_name":"anoctamin 10 [Source:HGNC Symbol;Acc:HGNC:25519]","synonyms":"TMEM16K,SCAR10,MGC47890,FLJ10375","biotype":"protein_coding","ncbi_id":"55129","summary":"The transmembrane protein encoded by this gene belongs to the anoctamin family of calcium-activated chloride channels, also known as the transmembrane 16 family. The encoded protein contains eight transmembrane domains with cytosolic N- and C-termini. Defects in this gene may cause autosomal recessive spinocerebellar ataxia-10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":43354859,"end":43691594,"strand":-1,"description":"anoctamin 10 [Source:HGNC Symbol;Acc:HGNC:25519]"}, {"versioned_ensembl_gene_id":"ENSG00000178586.5","gene_symbol":"OR6B3","gene_name":"olfactory receptor family 6 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:15042]","synonyms":"OR6B3Q,OR6B3P","biotype":"protein_coding","ncbi_id":"150681","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":240045077,"end":240047027,"strand":-1,"description":"olfactory receptor family 6 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:15042]"}, {"versioned_ensembl_gene_id":"ENSG00000255480.1","gene_symbol":"AL353699.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30425552,"end":30429268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256802.2","gene_symbol":"AC022613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29674990,"end":29680957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162222.13","gene_symbol":"TTC9C","gene_name":"tetratricopeptide repeat domain 9C [Source:HGNC Symbol;Acc:HGNC:28432]","synonyms":"MGC29649","biotype":"protein_coding","ncbi_id":"283237","summary":null,"start":62728069,"end":62740293,"strand":1,"description":"tetratricopeptide repeat domain 9C [Source:HGNC Symbol;Acc:HGNC:28432]"}, {"versioned_ensembl_gene_id":"ENSG00000174775.16","gene_symbol":"HRAS","gene_name":"HRas proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:5173]","synonyms":"HRAS1","biotype":"protein_coding","ncbi_id":"3265","summary":"This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, cognitive disability, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for this gene. [provided by RefSeq, Jul 2008]","start":532242,"end":537287,"strand":-1,"description":"HRas proto-oncogene, GTPase [Source:HGNC Symbol;Acc:HGNC:5173]"}, {"versioned_ensembl_gene_id":"ENSG00000114978.17","gene_symbol":"MOB1A","gene_name":"MOB kinase activator 1A [Source:HGNC Symbol;Acc:HGNC:16015]","synonyms":"MOBKL1B,MOBK1B,Mob4B,MOB1,Mats1,FLJ11595,FLJ10788,C2orf6","biotype":"protein_coding","ncbi_id":"55233","summary":"The protein encoded by this gene is a component of the Hippo signaling pathway, which controls organ size and tumor growth by enhancing apoptosis. Loss of the encoded protein results in cell proliferation and cancer formation. The encoded protein is also involved in the control of microtubule stability during cytokinesis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":74152528,"end":74178898,"strand":-1,"description":"MOB kinase activator 1A [Source:HGNC Symbol;Acc:HGNC:16015]"}, {"versioned_ensembl_gene_id":"ENSG00000140326.12","gene_symbol":"CDAN1","gene_name":"codanin 1 [Source:HGNC Symbol;Acc:HGNC:1713]","synonyms":"CDA-I,CDAI","biotype":"protein_coding","ncbi_id":"146059","summary":"This gene encodes a protein that appears to play a role in nuclear envelope integrity, possibly related to microtubule attachments. Mutations in this gene cause congenital dyserythropoietic anemia type I, a disease resulting in morphological and functional abnormalities of erythropoiesis. [provided by RefSeq, Jul 2009]","start":42723559,"end":42737126,"strand":-1,"description":"codanin 1 [Source:HGNC Symbol;Acc:HGNC:1713]"}, {"versioned_ensembl_gene_id":"ENSG00000259883.1","gene_symbol":"EHD4-AS1","gene_name":"EHD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51418]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928363","summary":null,"start":41921417,"end":41928883,"strand":1,"description":"EHD4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51418]"}, {"versioned_ensembl_gene_id":"ENSG00000214843.3","gene_symbol":"ZFYVE9P2","gene_name":"zinc finger FYVE-type containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39046]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420972","summary":null,"start":17284292,"end":17284895,"strand":1,"description":"zinc finger FYVE-type containing 9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39046]"}, {"versioned_ensembl_gene_id":"ENSG00000237170.3","gene_symbol":"RPS7P15","gene_name":"ribosomal protein S7 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:48878]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728015","summary":null,"start":4507078,"end":4507777,"strand":1,"description":"ribosomal protein S7 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:48878]"}, {"versioned_ensembl_gene_id":"ENSG00000217702.2","gene_symbol":"AC073263.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74130583,"end":74135395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255159.1","gene_symbol":"AC026894.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8768778,"end":8810231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215492.6","gene_symbol":"HNRNPA1P7","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31015]","synonyms":"HNRPA1L3","biotype":"processed_pseudogene","ncbi_id":"388275","summary":null,"start":32412214,"end":32413176,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:31015]"}, {"versioned_ensembl_gene_id":"ENSG00000264982.1","gene_symbol":"AC015563.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32287437,"end":32290340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265279.1","gene_symbol":"CLUHP6","gene_name":"clustered mitochondria homolog pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51571]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418754","summary":null,"start":32196026,"end":32196966,"strand":-1,"description":"clustered mitochondria homolog pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51571]"}, {"versioned_ensembl_gene_id":"ENSG00000237860.1","gene_symbol":"BX119904.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":116688870,"end":116690185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263917.1","gene_symbol":"AC011825.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32018829,"end":32111779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278493.1","gene_symbol":"AC039056.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41908204,"end":41908714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224200.2","gene_symbol":"FKBPL","gene_name":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]","synonyms":"DIR1,WISp39,NG7","biotype":"protein_coding","ncbi_id":"63943","summary":"The protein encoded by this gene has similarity to the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The encoded protein is thought to have a potential role in the induced radioresistance. Also it appears to have some involvement in the control of the cell cycle. [provided by RefSeq, Jul 2008]","start":32104478,"end":32106062,"strand":-1,"description":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]"}, {"versioned_ensembl_gene_id":"ENSG00000279166.1","gene_symbol":"AC009951.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":144494265,"end":144496878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213714.1","gene_symbol":"FAM209B","gene_name":"family with sequence similarity 209 member B [Source:HGNC Symbol;Acc:HGNC:16101]","synonyms":"dJ1153D9.4,C20orf107","biotype":"protein_coding","ncbi_id":"388799","summary":null,"start":56533246,"end":56536520,"strand":1,"description":"family with sequence similarity 209 member B [Source:HGNC Symbol;Acc:HGNC:16101]"}, {"versioned_ensembl_gene_id":"ENSG00000214097.4","gene_symbol":"SMCO1","gene_name":"single-pass membrane protein with coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:27407]","synonyms":"DKFZp313B0440,C3orf43,FLJ41923","biotype":"protein_coding","ncbi_id":"255798","summary":null,"start":196506877,"end":196515366,"strand":-1,"description":"single-pass membrane protein with coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:27407]"}, {"versioned_ensembl_gene_id":"ENSG00000125970.11","gene_symbol":"RALY","gene_name":"RALY heterogeneous nuclear ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:15921]","synonyms":"P542,HNRPCL2","biotype":"protein_coding","ncbi_id":"22913","summary":"This gene encodes a member of the heterogeneous nuclear ribonucleoprotein (hnRNP) gene family. This protein may play a role in pre-mRNA splicing and in embryonic development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":33993646,"end":34108308,"strand":1,"description":"RALY heterogeneous nuclear ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:15921]"}, {"versioned_ensembl_gene_id":"ENSG00000173068.17","gene_symbol":"BNC2","gene_name":"basonuclin 2 [Source:HGNC Symbol;Acc:HGNC:30988]","synonyms":"FLJ20043,BSN2","biotype":"protein_coding","ncbi_id":"54796","summary":"This gene encodes a conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. This gene is also associated with susceptibility to adolescent idiopathic scoliosis. [provided by RefSeq, Jul 2016]","start":16409503,"end":16870843,"strand":-1,"description":"basonuclin 2 [Source:HGNC Symbol;Acc:HGNC:30988]"}, {"versioned_ensembl_gene_id":"ENSG00000169826.7","gene_symbol":"CSGALNACT2","gene_name":"chondroitin sulfate N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:24292]","synonyms":"PRO0082,MGC40204,GALNACT2,GALNACT-2","biotype":"protein_coding","ncbi_id":"55454","summary":"This gene encodes a member of the chondroitin N-acetylgalactosaminyltransferase family. The encoded protein is involved in elongation during chondroitin sulfate synthesis. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome X. [provided by RefSeq, Feb 2016]","start":43138486,"end":43185308,"strand":1,"description":"chondroitin sulfate N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:24292]"}, {"versioned_ensembl_gene_id":"ENSG00000157578.13","gene_symbol":"LCA5L","gene_name":"LCA5L, lebercilin like [Source:HGNC Symbol;Acc:HGNC:1255]","synonyms":"MGC33295,C21orf13","biotype":"protein_coding","ncbi_id":"150082","summary":null,"start":39405844,"end":39445805,"strand":-1,"description":"LCA5L, lebercilin like [Source:HGNC Symbol;Acc:HGNC:1255]"}, {"versioned_ensembl_gene_id":"ENSG00000230694.1","gene_symbol":"AL450003.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16625676,"end":16626390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233551.2","gene_symbol":"LSM1P1","gene_name":"LSM1 homolog, mRNA degradation associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100820732","summary":null,"start":16775573,"end":16775845,"strand":-1,"description":"LSM1 homolog, mRNA degradation associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49776]"}, {"versioned_ensembl_gene_id":"ENSG00000270443.1","gene_symbol":"AL139344.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182433893,"end":182434461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255553.1","gene_symbol":"AP003733.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62077277,"end":62082184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254424.1","gene_symbol":"AP003733.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62072882,"end":62073052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214617.9","gene_symbol":"SLC6A10P","gene_name":"solute carrier family 6 member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:11043]","synonyms":"SLC6A10,CT-2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"386757","summary":null,"start":32877469,"end":32885501,"strand":-1,"description":"solute carrier family 6 member 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:11043]"}, {"versioned_ensembl_gene_id":"ENSG00000260047.2","gene_symbol":"BCAP31P2","gene_name":"B-cell receptor-associated protein 31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51324]","synonyms":"TCONS_l2_00009689","biotype":"unprocessed_pseudogene","ncbi_id":"100194426","summary":null,"start":32869985,"end":32873128,"strand":1,"description":"B-cell receptor-associated protein 31 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51324]"}, {"versioned_ensembl_gene_id":"ENSG00000241286.2","gene_symbol":"RPL29P25","gene_name":"ribosomal protein L29 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37039]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642493","summary":null,"start":110841538,"end":110842387,"strand":-1,"description":"ribosomal protein L29 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37039]"}, {"versioned_ensembl_gene_id":"ENSG00000257268.1","gene_symbol":"AC002375.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110831779,"end":110845963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275784.1","gene_symbol":"AL034549.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33989480,"end":33991818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259934.1","gene_symbol":"AC142086.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32845964,"end":32846180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230181.1","gene_symbol":"AL662826.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29579107,"end":29579624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228265.5","gene_symbol":"RALY-AS1","gene_name":"RALY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50743]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926888","summary":null,"start":33983052,"end":33994357,"strand":-1,"description":"RALY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50743]"}, {"versioned_ensembl_gene_id":"ENSG00000205549.8","gene_symbol":"C9orf92","gene_name":"chromosome 9 open reading frame 92 [Source:HGNC Symbol;Acc:HGNC:19054]","synonyms":"Em:AL513424.1","biotype":"protein_coding","ncbi_id":"100129385","summary":null,"start":16203935,"end":16276313,"strand":-1,"description":"chromosome 9 open reading frame 92 [Source:HGNC Symbol;Acc:HGNC:19054]"}, {"versioned_ensembl_gene_id":"ENSG00000279780.1","gene_symbol":"AC138907.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32786394,"end":32787379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168970.22","gene_symbol":"JMJD7-PLA2G4B","gene_name":"JMJD7-PLA2G4B readthrough [Source:HGNC Symbol;Acc:HGNC:34449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8681","summary":"This locus represents naturally-occurring readthrough transcription between the neighboring jumonji domain containing 7 (JMJD7) and phospholipase A2, group IVB (cytosolic) (PLA2G4B) genes. Readthrough transcripts encode fusion proteins that share amino acid sequence with each individual gene product, including a partial JmjC domain and downstream C2 and phospholipase A2 domains. Alternatively spliced transcript variants have been observed. [provided by RefSeq, Oct 2013]","start":41828095,"end":41848155,"strand":1,"description":"JMJD7-PLA2G4B readthrough [Source:HGNC Symbol;Acc:HGNC:34449]"}, {"versioned_ensembl_gene_id":"ENSG00000232344.2","gene_symbol":"AC087163.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18010643,"end":18011822,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189108.12","gene_symbol":"IL1RAPL2","gene_name":"interleukin 1 receptor accessory protein like 2 [Source:HGNC Symbol;Acc:HGNC:5997]","synonyms":"TIGIRR-1,IL1RAPL-2,IL1R9,IL-1R9","biotype":"protein_coding","ncbi_id":"26280","summary":"The protein encoded by this gene is a member of the interleukin 1 receptor family. This protein is similar to the interleukin 1 accessory proteins, and is most closely related to interleukin 1 receptor accessory protein-like 1 (IL1RAPL1). This gene and IL1RAPL1 are located at a region on chromosome X that is associated with X-linked non-syndromic cognitive disability. [provided by RefSeq, Jul 2008]","start":104566315,"end":105767829,"strand":1,"description":"interleukin 1 receptor accessory protein like 2 [Source:HGNC Symbol;Acc:HGNC:5997]"}, {"versioned_ensembl_gene_id":"ENSG00000261782.1","gene_symbol":"AC116553.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35879036,"end":35879498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104953.19","gene_symbol":"TLE6","gene_name":"transducin like enhancer of split 6 [Source:HGNC Symbol;Acc:HGNC:30788]","synonyms":"GRG6,FLJ14009","biotype":"protein_coding","ncbi_id":"79816","summary":"This gene encodes a member of the Groucho/ transducin-like Enhancer of split family of transcriptional co-repressors. The encoded protein is a component of the mammalian subcortical maternal complex, which is required for preimplantation development. In mouse, knock out of this gene results in cleavage-stage embryonic arrest resulting from defective cytoplasmic F-actin meshwork formation and asymmetric cell division. In human, an allelic variant in this gene is associated with preimplantation embryonic lethality. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":2977446,"end":2995184,"strand":1,"description":"transducin like enhancer of split 6 [Source:HGNC Symbol;Acc:HGNC:30788]"}, {"versioned_ensembl_gene_id":"ENSG00000219150.2","gene_symbol":"AL603914.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110706362,"end":110706882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230435.1","gene_symbol":"AC004160.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11406955,"end":11414078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232605.2","gene_symbol":"HMGN2P11","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:4990]","synonyms":"HMGN2L11,HMG17P1,28H","biotype":"processed_pseudogene","ncbi_id":"3152","summary":null,"start":84876554,"end":84876956,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:4990]"}, {"versioned_ensembl_gene_id":"ENSG00000239556.3","gene_symbol":"AC004951.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43984994,"end":43990207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228434.1","gene_symbol":"AC004951.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44004046,"end":44007866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241057.2","gene_symbol":"AC004951.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43961590,"end":43973323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123576.5","gene_symbol":"ESX1","gene_name":"ESX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14865]","synonyms":"ESXR1,ESX1L","biotype":"protein_coding","ncbi_id":"80712","summary":"This gene encodes a dual-function 65 kDa protein that undergoes proteolytic cleavage to produce a 45 kDa N-terminal fragment with a paired-like homeodomain and a 20 kDa C-terminal fragment with a proline-rich domain. The C-terminal fragment localizes to the cytoplasm while the N-terminal fragment localizes exclusively to the nucleus. In contrast to human, the mouse homolog has a novel PN/PF motif in the C-terminus and is paternally imprinted in placental tissue. This gene likely plays a role in placental development and spermatogenesis. [provided by RefSeq, Jan 2010]","start":104250038,"end":104254933,"strand":-1,"description":"ESX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:14865]"}, {"versioned_ensembl_gene_id":"ENSG00000278364.1","gene_symbol":"TRIAP1P1","gene_name":"TP53 regulated inhibitor of apoptosis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31659]","synonyms":"C10orf135,bA748L13.4","biotype":"processed_pseudogene","ncbi_id":"100289619","summary":null,"start":27425438,"end":27425662,"strand":-1,"description":"TP53 regulated inhibitor of apoptosis 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31659]"}, {"versioned_ensembl_gene_id":"ENSG00000124507.10","gene_symbol":"PACSIN1","gene_name":"protein kinase C and casein kinase substrate in neurons 1 [Source:HGNC Symbol;Acc:HGNC:8570]","synonyms":"SDPI","biotype":"protein_coding","ncbi_id":"29993","summary":null,"start":34466061,"end":34535231,"strand":1,"description":"protein kinase C and casein kinase substrate in neurons 1 [Source:HGNC Symbol;Acc:HGNC:8570]"}, {"versioned_ensembl_gene_id":"ENSG00000261307.1","gene_symbol":"AC102797.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47501172,"end":47558383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139278.9","gene_symbol":"GLIPR1","gene_name":"GLI pathogenesis related 1 [Source:HGNC Symbol;Acc:HGNC:17001]","synonyms":"RTVP1,GliPR","biotype":"protein_coding","ncbi_id":"11010","summary":"This gene encodes a protein with similarity to both the pathogenesis-related protein (PR) superfamily and the cysteine-rich secretory protein (CRISP) family. Increased expression of this gene is associated with myelomocytic differentiation in macrophage and decreased expression of this gene through gene methylation is associated with prostate cancer. The protein has proapoptotic activities in prostate and bladder cancer cells. This gene is a member of a cluster on chromosome 12 containing two other similar genes. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":75480680,"end":75503853,"strand":1,"description":"GLI pathogenesis related 1 [Source:HGNC Symbol;Acc:HGNC:17001]"}, {"versioned_ensembl_gene_id":"ENSG00000239927.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30319231,"end":30336806,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000115520.8","gene_symbol":"COQ10B","gene_name":"coenzyme Q10B [Source:HGNC Symbol;Acc:HGNC:25819]","synonyms":"FLJ13448","biotype":"protein_coding","ncbi_id":"80219","summary":null,"start":197453423,"end":197475308,"strand":1,"description":"coenzyme Q10B [Source:HGNC Symbol;Acc:HGNC:25819]"}, {"versioned_ensembl_gene_id":"ENSG00000281087.1","gene_symbol":"AC135068.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21709649,"end":21710270,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281113.1","gene_symbol":"AC135068.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21703428,"end":21705627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260522.1","gene_symbol":"AC106785.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35722268,"end":35722529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218476.2","gene_symbol":"AL591416.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23102680,"end":23103546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260500.1","gene_symbol":"AC010336.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7918652,"end":7919157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115282.19","gene_symbol":"TTC31","gene_name":"tetratricopeptide repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:25759]","synonyms":"FLJ12788","biotype":"protein_coding","ncbi_id":"64427","summary":null,"start":74483073,"end":74494886,"strand":1,"description":"tetratricopeptide repeat domain 31 [Source:HGNC Symbol;Acc:HGNC:25759]"}, {"versioned_ensembl_gene_id":"ENSG00000263275.1","gene_symbol":"AL513523.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153768214,"end":153769407,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282348.1","gene_symbol":"AC003976.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36116566,"end":36177866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196154.11","gene_symbol":"S100A4","gene_name":"S100 calcium binding protein A4 [Source:HGNC Symbol;Acc:HGNC:10494]","synonyms":"PEL98,P9KA,MTS1,FSP1,CAPL,42A,18A2","biotype":"protein_coding","ncbi_id":"6275","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in motility, invasion, and tubulin polymerization. Chromosomal rearrangements and altered expression of this gene have been implicated in tumor metastasis. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":153543613,"end":153550136,"strand":-1,"description":"S100 calcium binding protein A4 [Source:HGNC Symbol;Acc:HGNC:10494]"}, {"versioned_ensembl_gene_id":"ENSG00000258895.1","gene_symbol":"AC104390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94033658,"end":94034177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266908.1","gene_symbol":"AL109935.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5499116,"end":5502881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225836.1","gene_symbol":"AL157400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89646289,"end":89650822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257135.5","gene_symbol":"AC007249.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10448694,"end":10451327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175841.8","gene_symbol":"FAM172BP","gene_name":"family with sequence similarity 172 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:34336]","synonyms":"LOC131909,FLJ45679,FAM172B","biotype":"processed_pseudogene","ncbi_id":"131909","summary":null,"start":101521891,"end":101522979,"strand":1,"description":"family with sequence similarity 172 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:34336]"}, {"versioned_ensembl_gene_id":"ENSG00000277600.4","gene_symbol":"CNOT3","gene_name":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]","synonyms":"NOT3,LENG2,KIAA0691,NOT3H,NOT3,LENG2,KIAA0691,NOT3H","biotype":"protein_coding","ncbi_id":"4849","summary":null,"start":54138190,"end":54156165,"strand":1,"description":"CCR4-NOT transcription complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7879]"}, {"versioned_ensembl_gene_id":"ENSG00000277477.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54717647,"end":54721610,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000168826.15","gene_symbol":"ZBTB49","gene_name":"zinc finger and BTB domain containing 49 [Source:HGNC Symbol;Acc:HGNC:19883]","synonyms":"ZNF509,FLJ38559","biotype":"protein_coding","ncbi_id":"166793","summary":null,"start":4290251,"end":4321786,"strand":1,"description":"zinc finger and BTB domain containing 49 [Source:HGNC Symbol;Acc:HGNC:19883]"}, {"versioned_ensembl_gene_id":"ENSG00000282685.1","gene_symbol":"FAM83H-AS1","gene_name":"FAM83H antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48720]","synonyms":"onco-lncRNA-3","biotype":"processed_transcript","ncbi_id":"100128338","summary":null,"start":143721147,"end":143733344,"strand":1,"description":"FAM83H antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48720]"}, {"versioned_ensembl_gene_id":"ENSG00000129824.15","gene_symbol":"RPS4Y1","gene_name":"ribosomal protein S4, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:10425]","synonyms":"S4,RPS4Y,MGC5070,MGC119100","biotype":"protein_coding","ncbi_id":"6192","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes ribosomal protein S4, a component of the 40S subunit. Ribosomal protein S4 is the only ribosomal protein known to be encoded by more than one gene, namely this gene and ribosomal protein S4, X-linked (RPS4X). The 2 isoforms encoded by these genes are not identical, but are functionally equivalent. Ribosomal protein S4 belongs to the S4E family of ribosomal proteins. It has been suggested that haploinsufficiency of the ribosomal protein S4 genes plays a role in Turner syndrome; however, this hypothesis is controversial. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":2841486,"end":2932000,"strand":1,"description":"ribosomal protein S4, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:10425]"}, {"versioned_ensembl_gene_id":"ENSG00000133116.7","gene_symbol":"KL","gene_name":"klotho [Source:HGNC Symbol;Acc:HGNC:6344]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9365","summary":"This gene encodes a type-I membrane protein that is related to beta-glucosidases. Reduced production of this protein has been observed in patients with chronic renal failure (CRF), and this may be one of the factors underlying the degenerative processes (e.g., arteriosclerosis, osteoporosis, and skin atrophy) seen in CRF. Also, mutations within this protein have been associated with ageing and bone loss. [provided by RefSeq, Jul 2008]","start":33016433,"end":33066145,"strand":1,"description":"klotho [Source:HGNC Symbol;Acc:HGNC:6344]"}, {"versioned_ensembl_gene_id":"ENSG00000273681.1","gene_symbol":"FAM210CP","gene_name":"family with sequence similarity 210 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131328","summary":null,"start":27397017,"end":27397590,"strand":-1,"description":"family with sequence similarity 210 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:44938]"}, {"versioned_ensembl_gene_id":"ENSG00000235244.3","gene_symbol":"DANT2","gene_name":"DXZ4 associated non-coding transcript 2, distal [Source:HGNC Symbol;Acc:HGNC:50862]","synonyms":null,"biotype":"lincRNA","ncbi_id":"642776","summary":null,"start":115917271,"end":115969089,"strand":-1,"description":"DXZ4 associated non-coding transcript 2, distal [Source:HGNC Symbol;Acc:HGNC:50862]"}, {"versioned_ensembl_gene_id":"ENSG00000227604.3","gene_symbol":"TOMM22P3","gene_name":"TOMM22 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38739]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"122038","summary":null,"start":32954057,"end":32954401,"strand":-1,"description":"TOMM22 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38739]"}, {"versioned_ensembl_gene_id":"ENSG00000164007.10","gene_symbol":"CLDN19","gene_name":"claudin 19 [Source:HGNC Symbol;Acc:HGNC:2040]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149461","summary":"The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]","start":42733093,"end":42740254,"strand":-1,"description":"claudin 19 [Source:HGNC Symbol;Acc:HGNC:2040]"}, {"versioned_ensembl_gene_id":"ENSG00000146938.14","gene_symbol":"NLGN4X","gene_name":"neuroligin 4, X-linked [Source:HGNC Symbol;Acc:HGNC:14287]","synonyms":"NLGN4,NLGN,KIAA1260,HLNX","biotype":"protein_coding","ncbi_id":"57502","summary":"This gene encodes a member of the type-B carboxylesterase/lipase protein family. The encoded protein belongs to a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. The encoded protein interacts with discs large homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":5840637,"end":6228863,"strand":-1,"description":"neuroligin 4, X-linked [Source:HGNC Symbol;Acc:HGNC:14287]"}, {"versioned_ensembl_gene_id":"ENSG00000095713.13","gene_symbol":"CRTAC1","gene_name":"cartilage acidic protein 1 [Source:HGNC Symbol;Acc:HGNC:14882]","synonyms":"FLJ10320,CEP-68,ASPIC1","biotype":"protein_coding","ncbi_id":"55118","summary":"This gene encodes a glycosylated extracellular matrix protein that is found in the interterritorial matrix of articular deep zone cartilage. This protein is used as a marker to distinguish chondrocytes from osteoblasts and mesenchymal stem cells in culture. The presence of FG-GAP motifs and an RGD integrin-binding motif suggests that this protein may be involved in cell-cell or cell-matrix interactions. Copy number alterations in this gene have been observed in neurofibromatosis type 1-associated glomus tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":97865000,"end":98030828,"strand":-1,"description":"cartilage acidic protein 1 [Source:HGNC Symbol;Acc:HGNC:14882]"}, {"versioned_ensembl_gene_id":"ENSG00000227871.1","gene_symbol":"USP9YP12","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38720]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874382","summary":null,"start":23945927,"end":23952293,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:38720]"}, {"versioned_ensembl_gene_id":"ENSG00000206502.8","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"hZR14,tctex-6,RPA12,HTEX-6","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30048487,"end":30054477,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000234140.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BAT1P2,BPG309N1.15","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29982616,"end":29983011,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000155265.10","gene_symbol":"GOLGA7B","gene_name":"golgin A7 family member B [Source:HGNC Symbol;Acc:HGNC:31668]","synonyms":"C10orf133,C10orf132,bA459F3.4,bA451M19.3","biotype":"protein_coding","ncbi_id":"401647","summary":null,"start":97850239,"end":97871580,"strand":1,"description":"golgin A7 family member B [Source:HGNC Symbol;Acc:HGNC:31668]"}, {"versioned_ensembl_gene_id":"ENSG00000260845.1","gene_symbol":"AC138907.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32735909,"end":32741094,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233076.6","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31766492,"end":31770071,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000232195.1","gene_symbol":"TOMM22P2","gene_name":"TOMM22 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499417","summary":null,"start":2827982,"end":2828218,"strand":1,"description":"TOMM22 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38737]"}, {"versioned_ensembl_gene_id":"ENSG00000213973.8","gene_symbol":"ZNF99","gene_name":"zinc finger protein 99 [Source:HGNC Symbol;Acc:HGNC:13175]","synonyms":"MGC24986,C19orf9","biotype":"protein_coding","ncbi_id":"7652","summary":null,"start":22752183,"end":22784107,"strand":-1,"description":"zinc finger protein 99 [Source:HGNC Symbol;Acc:HGNC:13175]"}, {"versioned_ensembl_gene_id":"ENSG00000104142.10","gene_symbol":"VPS18","gene_name":"VPS18, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:15972]","synonyms":"PEP3,KIAA1475","biotype":"protein_coding","ncbi_id":"57617","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps18 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. [provided by RefSeq, Jul 2008]","start":40894430,"end":40903975,"strand":1,"description":"VPS18, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:15972]"}, {"versioned_ensembl_gene_id":"ENSG00000232632.8","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"hGB1a,GPRC3A","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29552212,"end":29629760,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000133392.17","gene_symbol":"MYH11","gene_name":"myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]","synonyms":"SMMHC,SMHC","biotype":"protein_coding","ncbi_id":"4629","summary":"The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alternative splicing generates isoforms that are differentially expressed, with ratios changing during muscle cell maturation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":15703172,"end":15857033,"strand":-1,"description":"myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]"}, {"versioned_ensembl_gene_id":"ENSG00000235663.1","gene_symbol":"SAPCD1-AS1","gene_name":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]","synonyms":"C6orf26-AS1","biotype":"antisense_RNA","ncbi_id":"104413891","summary":null,"start":31764310,"end":31765588,"strand":-1,"description":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]"}, {"versioned_ensembl_gene_id":"ENSG00000261445.1","gene_symbol":"AC018558.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35493754,"end":35496457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281289.2","gene_symbol":"LSS","gene_name":"lanosterol synthase [Source:HGNC Symbol;Acc:HGNC:6708]","synonyms":"OSC","biotype":"protein_coding","ncbi_id":"4047","summary":"The protein encoded by this gene catalyzes the conversion of (S)-2,3 oxidosqualene to lanosterol. The encoded protein is a member of the terpene cyclase/mutase family and catalyzes the first step in the biosynthesis of cholesterol, steroid hormones, and vitamin D. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2009]","start":46190452,"end":46221883,"strand":-1,"description":"lanosterol synthase [Source:HGNC Symbol;Acc:HGNC:6708]"}, {"versioned_ensembl_gene_id":"ENSG00000141452.9","gene_symbol":"C18orf8","gene_name":"chromosome 18 open reading frame 8 [Source:HGNC Symbol;Acc:HGNC:24326]","synonyms":"MIC1,MIC-1,HsT2591","biotype":"protein_coding","ncbi_id":"29919","summary":"This gene encodes a colon cancer associated protein. [provided by RefSeq, Jan 2013]","start":23503470,"end":23531807,"strand":1,"description":"chromosome 18 open reading frame 8 [Source:HGNC Symbol;Acc:HGNC:24326]"}, {"versioned_ensembl_gene_id":"ENSG00000275626.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54835435,"end":54852194,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000130414.11","gene_symbol":"NDUFA10","gene_name":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]","synonyms":"CI-42k","biotype":"protein_coding","ncbi_id":"4705","summary":"The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]","start":239892450,"end":240025402,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A10 [Source:HGNC Symbol;Acc:HGNC:7684]"}, {"versioned_ensembl_gene_id":"ENSG00000224571.1","gene_symbol":"USP9YP13","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38721]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100861434","summary":null,"start":23919905,"end":23921510,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38721]"}, {"versioned_ensembl_gene_id":"ENSG00000282074.1","gene_symbol":"AC243733.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":15480860,"end":15600484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162927.13","gene_symbol":"PUS10","gene_name":"pseudouridylate synthase 10 [Source:HGNC Symbol;Acc:HGNC:26505]","synonyms":"FLJ32312,CCDC139","biotype":"protein_coding","ncbi_id":"150962","summary":"Pseudouridination, the isomerization of uridine to pseudouridine, is the most common posttranscriptional nucleotide modification found in RNA and is essential for biologic functions such as spliceosome biogenesis. Pseudouridylate synthases, such as PUS10, catalyze pseudouridination of structural RNAs, including transfer, ribosomal, and splicing RNAs. These enzymes also act as RNA chaperones, facilitating the correct folding and assembly of tRNAs (McCleverty et al., 2007 [PubMed 17900615]).[supplied by OMIM, May 2009]","start":60940222,"end":61018259,"strand":-1,"description":"pseudouridylate synthase 10 [Source:HGNC Symbol;Acc:HGNC:26505]"}, {"versioned_ensembl_gene_id":"ENSG00000114346.13","gene_symbol":"ECT2","gene_name":"epithelial cell transforming 2 [Source:HGNC Symbol;Acc:HGNC:3155]","synonyms":"ARHGEF31","biotype":"protein_coding","ncbi_id":"1894","summary":"The protein encoded by this gene is a guanine nucleotide exchange factor and transforming protein that is related to Rho-specific exchange factors and yeast cell cycle regulators. The expression of this gene is elevated with the onset of DNA synthesis and remains elevated during G2 and M phases. In situ hybridization analysis showed that expression is at a high level in cells undergoing mitosis in regenerating liver. Thus, this protein is expressed in a cell cycle-dependent manner during liver regeneration, and is thought to have an important role in the regulation of cytokinesis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2017]","start":172750682,"end":172821474,"strand":1,"description":"epithelial cell transforming 2 [Source:HGNC Symbol;Acc:HGNC:3155]"}, {"versioned_ensembl_gene_id":"ENSG00000228335.1","gene_symbol":"AC073063.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99442890,"end":99443496,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228132.2","gene_symbol":"AL360221.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6276640,"end":6276974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264296.1","gene_symbol":"AC090666.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54142133,"end":54142577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223658.7","gene_symbol":"C1GALT1C1L","gene_name":"C1GALT1-specific chaperone 1 like [Source:HGNC Symbol;Acc:HGNC:51617]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728819","summary":null,"start":43675151,"end":43676322,"strand":-1,"description":"C1GALT1-specific chaperone 1 like [Source:HGNC Symbol;Acc:HGNC:51617]"}, {"versioned_ensembl_gene_id":"ENSG00000006007.11","gene_symbol":"GDE1","gene_name":"glycerophosphodiester phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:29644]","synonyms":"MIR16","biotype":"protein_coding","ncbi_id":"51573","summary":null,"start":19501689,"end":19522145,"strand":-1,"description":"glycerophosphodiester phosphodiesterase 1 [Source:HGNC Symbol;Acc:HGNC:29644]"}, {"versioned_ensembl_gene_id":"ENSG00000279747.1","gene_symbol":"AC130456.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19503861,"end":19504625,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278279.4","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"CD85k,LIR-5,ILT3,HM18,LIR5","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54414251,"end":54422496,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000184304.14","gene_symbol":"PRKD1","gene_name":"protein kinase D1 [Source:HGNC Symbol;Acc:HGNC:9407]","synonyms":"PRKCM,PKD,PKCM,PKC-mu","biotype":"protein_coding","ncbi_id":"5587","summary":"The protein encoded by this gene is a serine/threonine protein kinase involved in many cellular processes, including Golgi body membrane integrity and transport, cell migration and differentiation, MAPK8/JNK1 and Ras pathway signaling, MAPK1/3 (ERK1/2) pathway signaling, cell survival, and regulation of cell shape and adhesion. [provided by RefSeq, Jan 2017]","start":29576479,"end":30191898,"strand":-1,"description":"protein kinase D1 [Source:HGNC Symbol;Acc:HGNC:9407]"}, {"versioned_ensembl_gene_id":"ENSG00000213272.5","gene_symbol":"RPL7AP9","gene_name":"ribosomal protein L7a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:32398]","synonyms":"RPL7AP59","biotype":"processed_pseudogene","ncbi_id":"441642","summary":null,"start":76599671,"end":76600470,"strand":1,"description":"ribosomal protein L7a pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:32398]"}, {"versioned_ensembl_gene_id":"ENSG00000230562.3","gene_symbol":"FAM133DP","gene_name":"family with sequence similarity 133 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:44192]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728066","summary":null,"start":157379724,"end":157380414,"strand":-1,"description":"family with sequence similarity 133 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:44192]"}, {"versioned_ensembl_gene_id":"ENSG00000257060.6","gene_symbol":"AC091078.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93312557,"end":93569483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187172.15","gene_symbol":"BAGE2","gene_name":"BAGE family member 2 [Source:HGNC Symbol;Acc:HGNC:15723]","synonyms":"CT2.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"85319","summary":null,"start":10413477,"end":10516431,"strand":1,"description":"BAGE family member 2 [Source:HGNC Symbol;Acc:HGNC:15723]"}, {"versioned_ensembl_gene_id":"ENSG00000276662.1","gene_symbol":"AL713922.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":147820,"end":148751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258909.1","gene_symbol":"AC091078.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93416850,"end":93422576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258787.1","gene_symbol":"AC091078.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93430659,"end":93431217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242097.1","gene_symbol":"AC068647.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151759747,"end":151762011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282617.1","gene_symbol":"AC105219.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143705253,"end":143705898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143458.11","gene_symbol":"GABPB2","gene_name":"GA binding protein transcription factor beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:28441]","synonyms":"MGC29891","biotype":"protein_coding","ncbi_id":"126626","summary":null,"start":151070578,"end":151125542,"strand":1,"description":"GA binding protein transcription factor beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:28441]"}, {"versioned_ensembl_gene_id":"ENSG00000258249.1","gene_symbol":"AC125603.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116599270,"end":116603585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257883.1","gene_symbol":"AC125603.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116661582,"end":116698065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275932.2","gene_symbol":"DUSP14","gene_name":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]","synonyms":"MKP6,MKP-L","biotype":"protein_coding","ncbi_id":"11072","summary":"Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP14 contains the consensus DUSP C-terminal catalytic domain but lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]","start":37494470,"end":37518136,"strand":1,"description":"dual specificity phosphatase 14 [Source:HGNC Symbol;Acc:HGNC:17007]"}, {"versioned_ensembl_gene_id":"ENSG00000274414.1","gene_symbol":"AL121772.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25239007,"end":25245229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223525.1","gene_symbol":"RABGAP1L-IT1","gene_name":"RABGAP1L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41471]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480742","summary":null,"start":174896958,"end":174897996,"strand":1,"description":"RABGAP1L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41471]"}, {"versioned_ensembl_gene_id":"ENSG00000236398.2","gene_symbol":"TAS2R39","gene_name":"taste 2 receptor member 39 [Source:HGNC Symbol;Acc:HGNC:18886]","synonyms":null,"biotype":"protein_coding","ncbi_id":"259285","summary":"The protein encoded by this gene is a bitter taste receptor that detects green tea catechins, soy isoflavones, and theaflavins. The encoded protein is gustducin-linked and may activate alpha gustducin. This gene is intronless. [provided by RefSeq, Dec 2015]","start":143183419,"end":143184435,"strand":1,"description":"taste 2 receptor member 39 [Source:HGNC Symbol;Acc:HGNC:18886]"}, {"versioned_ensembl_gene_id":"ENSG00000245748.1","gene_symbol":"AC097382.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7030554,"end":7046231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274352.4","gene_symbol":"ZNF707","gene_name":"zinc finger protein 707 [Source:HGNC Symbol;Acc:HGNC:27815]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286075","summary":null,"start":143671459,"end":143700905,"strand":1,"description":"zinc finger protein 707 [Source:HGNC Symbol;Acc:HGNC:27815]"}, {"versioned_ensembl_gene_id":"ENSG00000257426.1","gene_symbol":"AC126177.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":107899638,"end":107899815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257398.6","gene_symbol":"AC126177.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107839291,"end":107864562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143556.8","gene_symbol":"S100A7","gene_name":"S100 calcium binding protein A7 [Source:HGNC Symbol;Acc:HGNC:10497]","synonyms":"S100A7c,PSOR1","biotype":"protein_coding","ncbi_id":"6278","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein differs from the other S100 proteins of known structure in its lack of calcium binding ability in one EF-hand at the N-terminus. The protein is overexpressed in hyperproliferative skin diseases, exhibits antimicrobial activities against bacteria and induces immunomodulatory activities. [provided by RefSeq, Nov 2014]","start":153457744,"end":153460701,"strand":-1,"description":"S100 calcium binding protein A7 [Source:HGNC Symbol;Acc:HGNC:10497]"}, {"versioned_ensembl_gene_id":"ENSG00000196668.3","gene_symbol":"LINC00173","gene_name":"long intergenic non-protein coding RNA 173 [Source:HGNC Symbol;Acc:HGNC:33791]","synonyms":"NCRNA00173,FLJ42957","biotype":"processed_transcript","ncbi_id":"100287569","summary":null,"start":116533422,"end":116536518,"strand":1,"description":"long intergenic non-protein coding RNA 173 [Source:HGNC Symbol;Acc:HGNC:33791]"}, {"versioned_ensembl_gene_id":"ENSG00000070610.14","gene_symbol":"GBA2","gene_name":"glucosylceramidase beta 2 [Source:HGNC Symbol;Acc:HGNC:18986]","synonyms":"SPG46,KIAA1605,DKFZp762K054,AD035","biotype":"protein_coding","ncbi_id":"57704","summary":"This gene encodes a microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. Studies to determine subcellular localization of this protein in the liver indicated that the enzyme was mainly enriched in the microsomal fraction where it appeared to be confined to the endoplasmic reticulum. This putative transmembrane protein is thought to play a role in carbohydrate transport and metabolism. [provided by RefSeq, Jul 2008]","start":35736866,"end":35749228,"strand":-1,"description":"glucosylceramidase beta 2 [Source:HGNC Symbol;Acc:HGNC:18986]"}, {"versioned_ensembl_gene_id":"ENSG00000151303.11","gene_symbol":"AL136982.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":86992406,"end":87010203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261011.1","gene_symbol":"AL136982.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":87001636,"end":87009905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187904.3","gene_symbol":"AC097382.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":6995341,"end":6998958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188976.10","gene_symbol":"NOC2L","gene_name":"NOC2 like nucleolar associated transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:24517]","synonyms":"PPP1R112,NIR,NET7,NET15,DKFZP564C186","biotype":"protein_coding","ncbi_id":"26155","summary":"Histone modification by histone acetyltransferases (HAT) and histone deacetylases (HDAC) can control major aspects of transcriptional regulation. NOC2L represents a novel HDAC-independent inhibitor of histone acetyltransferase (INHAT) (Hublitz et al., 2005 [PubMed 16322561]).[supplied by OMIM, Mar 2008]","start":944204,"end":959309,"strand":-1,"description":"NOC2 like nucleolar associated transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:24517]"}, {"versioned_ensembl_gene_id":"ENSG00000158417.10","gene_symbol":"EIF5B","gene_name":"eukaryotic translation initiation factor 5B [Source:HGNC Symbol;Acc:HGNC:30793]","synonyms":"KIAA0741,IF2,FLJ10524,DKFZp434I036","biotype":"protein_coding","ncbi_id":"9669","summary":"Accurate initiation of translation in eukaryotes is complex and requires many factors, some of which are composed of multiple subunits. The process is simpler in prokaryotes which have only three initiation factors (IF1, IF2, IF3). Two of these factors are conserved in eukaryotes: the homolog of IF1 is eIF1A and the homolog of IF2 is eIF5B. This gene encodes eIF5B. Factors eIF1A and eIF5B interact on the ribosome along with other initiation factors and GTP to position the initiation methionine tRNA on the start codon of the mRNA so that translation initiates accurately. [provided by RefSeq, Jul 2008]","start":99337353,"end":99401326,"strand":1,"description":"eukaryotic translation initiation factor 5B [Source:HGNC Symbol;Acc:HGNC:30793]"}, {"versioned_ensembl_gene_id":"ENSG00000224144.1","gene_symbol":"ASH2LP1","gene_name":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19332]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266703","summary":null,"start":22420326,"end":22421310,"strand":1,"description":"ASH2 like histone lysine methyltransferase complex subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19332]"}, {"versioned_ensembl_gene_id":"ENSG00000225598.1","gene_symbol":"AL606519.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80373364,"end":80374621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000015171.19","gene_symbol":"ZMYND11","gene_name":"zinc finger MYND-type containing 11 [Source:HGNC Symbol;Acc:HGNC:16966]","synonyms":"BS69","biotype":"protein_coding","ncbi_id":"10771","summary":"The protein encoded by this gene was first identified by its ability to bind the adenovirus E1A protein. The protein localizes to the nucleus. It functions as a transcriptional repressor, and expression of E1A inhibits this repression. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":134465,"end":254637,"strand":1,"description":"zinc finger MYND-type containing 11 [Source:HGNC Symbol;Acc:HGNC:16966]"}, {"versioned_ensembl_gene_id":"ENSG00000147509.13","gene_symbol":"RGS20","gene_name":"regulator of G protein signaling 20 [Source:HGNC Symbol;Acc:HGNC:14600]","synonyms":"ZGAP1,RGSZ1","biotype":"protein_coding","ncbi_id":"8601","summary":"The protein encoded by this gene belongs to the family of regulator of G protein signaling (RGS) proteins, which are regulatory and structural components of G protein-coupled receptor complexes. RGS proteins inhibit signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound forms. This protein selectively binds to G(z)-alpha and G(alpha)-i2 subunits, and regulates their signaling activities. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":53851808,"end":53959303,"strand":1,"description":"regulator of G protein signaling 20 [Source:HGNC Symbol;Acc:HGNC:14600]"}, {"versioned_ensembl_gene_id":"ENSG00000224444.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"OTTHUMG00000086553,MAS1LP","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29471596,"end":29472642,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000256806.5","gene_symbol":"C17orf100","gene_name":"chromosome 17 open reading frame 100 [Source:HGNC Symbol;Acc:HGNC:34494]","synonyms":"LOC388327","biotype":"protein_coding","ncbi_id":"388327","summary":null,"start":6651718,"end":6693202,"strand":1,"description":"chromosome 17 open reading frame 100 [Source:HGNC Symbol;Acc:HGNC:34494]"}, {"versioned_ensembl_gene_id":"ENSG00000165733.7","gene_symbol":"BMS1","gene_name":"BMS1, ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:23505]","synonyms":"KIAA0187,BMS1L","biotype":"protein_coding","ncbi_id":"9790","summary":"This gene likely encodes a ribosome assembly protein. A similar protein in yeast functions in 35S-rRNA processing, which includes a series of cleavage steps critical for formation of 40S ribosomes. Related pseudogenes exist on chromosomes 2, 9, 10, 15, 16, and 22.[provided by RefSeq, Mar 2009]","start":42782801,"end":42834937,"strand":1,"description":"BMS1, ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:23505]"}, {"versioned_ensembl_gene_id":"ENSG00000260680.1","gene_symbol":"AGGF1P5","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51741]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128103","summary":null,"start":35420291,"end":35421209,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51741]"}, {"versioned_ensembl_gene_id":"ENSG00000229695.1","gene_symbol":"AC011242.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43680465,"end":43681622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111405.8","gene_symbol":"ENDOU","gene_name":"endonuclease, poly(U) specific [Source:HGNC Symbol;Acc:HGNC:14369]","synonyms":"PRSS26,PP11,P11","biotype":"protein_coding","ncbi_id":"8909","summary":"This gene encodes a protein with endoribonuclease activity that binds polyuridine-enriched single-stranded RNA. This gene was initially characterized based on its high expression in placenta but was mischaracterized as a serine protease. In mouse, this gene promotes tolerance to self-antigens by regulating B cell activation-induced cell death (AICD). The protein may be useful as a tumor marker. Multiple alternatively spliced transcript variants encoding distinct protein isoforms have been found for this gene. [provided by RefSeq, Jul 2020]","start":47709734,"end":47725567,"strand":-1,"description":"endonuclease, poly(U) specific [Source:HGNC Symbol;Acc:HGNC:14369]"}, {"versioned_ensembl_gene_id":"ENSG00000241120.1","gene_symbol":"HMGN1P8","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874431","summary":null,"start":167694355,"end":167694642,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39351]"}, {"versioned_ensembl_gene_id":"ENSG00000183617.4","gene_symbol":"MRPL54","gene_name":"mitochondrial ribosomal protein L54 [Source:HGNC Symbol;Acc:HGNC:16685]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116541","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":3762664,"end":3768575,"strand":1,"description":"mitochondrial ribosomal protein L54 [Source:HGNC Symbol;Acc:HGNC:16685]"}, {"versioned_ensembl_gene_id":"ENSG00000234917.2","gene_symbol":"AC098484.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42678735,"end":42681659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125998.7","gene_symbol":"FAM83C","gene_name":"family with sequence similarity 83 member C [Source:HGNC Symbol;Acc:HGNC:16121]","synonyms":"dJ614O4.7,C20orf128","biotype":"protein_coding","ncbi_id":"128876","summary":"This gene encodes a member of the family with sequence similarity 83 protein family. The encoded protein may be involved in regulating MAPK signaling in cancer cells. [provided by RefSeq, Mar 2017]","start":35285731,"end":35292401,"strand":-1,"description":"family with sequence similarity 83 member C [Source:HGNC Symbol;Acc:HGNC:16121]"}, {"versioned_ensembl_gene_id":"ENSG00000186328.4","gene_symbol":"AL451165.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34715613,"end":34715940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238040.1","gene_symbol":"SALL4P2","gene_name":"spalt like transcription factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130259","summary":null,"start":129871309,"end":129877567,"strand":1,"description":"spalt like transcription factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39819]"}, {"versioned_ensembl_gene_id":"ENSG00000253483.1","gene_symbol":"AC104561.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23483016,"end":23483534,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272973.1","gene_symbol":"AP000350.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23856427,"end":23857039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068796.16","gene_symbol":"KIF2A","gene_name":"kinesin family member 2A [Source:HGNC Symbol;Acc:HGNC:6318]","synonyms":"KIF2,HK2","biotype":"protein_coding","ncbi_id":"3796","summary":"The protein encoded by this gene is a plus end-directed motor required for normal mitotic progression. The encoded protein is required for normal spindle activity during mitosis and is necessary for normal brain development. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":62306162,"end":62537249,"strand":1,"description":"kinesin family member 2A [Source:HGNC Symbol;Acc:HGNC:6318]"}, {"versioned_ensembl_gene_id":"ENSG00000171792.10","gene_symbol":"RHNO1","gene_name":"RAD9-HUS1-RAD1 interacting nuclear orphan 1 [Source:HGNC Symbol;Acc:HGNC:28206]","synonyms":"RHINO,MGC13204,HKMT1188,C12orf32","biotype":"protein_coding","ncbi_id":"83695","summary":null,"start":2876258,"end":2889523,"strand":1,"description":"RAD9-HUS1-RAD1 interacting nuclear orphan 1 [Source:HGNC Symbol;Acc:HGNC:28206]"}, {"versioned_ensembl_gene_id":"ENSG00000215845.10","gene_symbol":"TSTD1","gene_name":"thiosulfate sulfurtransferase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:35410]","synonyms":"KAT","biotype":"protein_coding","ncbi_id":"100131187","summary":null,"start":161037631,"end":161038990,"strand":-1,"description":"thiosulfate sulfurtransferase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:35410]"}, {"versioned_ensembl_gene_id":"ENSG00000261263.2","gene_symbol":"AC138907.5","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32650195,"end":32650910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261111.1","gene_symbol":"AC133569.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32635673,"end":32636045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270516.1","gene_symbol":"AC079791.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119178177,"end":119179149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230520.1","gene_symbol":"AC092098.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118950386,"end":118951259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103111.14","gene_symbol":"MON1B","gene_name":"MON1 homolog B, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:25020]","synonyms":"HSRG1,SAND2,KIAA0872","biotype":"protein_coding","ncbi_id":"22879","summary":null,"start":77190835,"end":77202405,"strand":1,"description":"MON1 homolog B, secretory trafficking associated [Source:HGNC Symbol;Acc:HGNC:25020]"}, {"versioned_ensembl_gene_id":"ENSG00000231131.6","gene_symbol":"LINC01468","gene_name":"long intergenic non-protein coding RNA 1468 [Source:HGNC Symbol;Acc:HGNC:50913]","synonyms":"lnc-MBL2-4","biotype":"lincRNA","ncbi_id":"101928687","summary":null,"start":52450874,"end":52470533,"strand":-1,"description":"long intergenic non-protein coding RNA 1468 [Source:HGNC Symbol;Acc:HGNC:50913]"}, {"versioned_ensembl_gene_id":"ENSG00000279452.1","gene_symbol":"AC006277.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2949035,"end":2950644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087589.16","gene_symbol":"CASS4","gene_name":"Cas scaffolding protein family member 4 [Source:HGNC Symbol;Acc:HGNC:15878]","synonyms":"HEPL,HEFL,C20orf32","biotype":"protein_coding","ncbi_id":"57091","summary":null,"start":56412112,"end":56460387,"strand":1,"description":"Cas scaffolding protein family member 4 [Source:HGNC Symbol;Acc:HGNC:15878]"}, {"versioned_ensembl_gene_id":"ENSG00000227459.1","gene_symbol":"AC079612.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239625698,"end":239630839,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220721.2","gene_symbol":"OR1F12","gene_name":"olfactory receptor family 1 subfamily F member 12 [Source:HGNC Symbol;Acc:HGNC:13964]","synonyms":"OR1F12Q,OR1F12P,hs6M1-35P","biotype":"unprocessed_pseudogene","ncbi_id":"442179","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":28073316,"end":28074260,"strand":1,"description":"olfactory receptor family 1 subfamily F member 12 [Source:HGNC Symbol;Acc:HGNC:13964]"}, {"versioned_ensembl_gene_id":"ENSG00000261233.2","gene_symbol":"ABCD1P3","gene_name":"ATP binding cassette subfamily D member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:64]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"26982","summary":null,"start":32475051,"end":32478250,"strand":-1,"description":"ATP binding cassette subfamily D member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:64]"}, {"versioned_ensembl_gene_id":"ENSG00000260662.2","gene_symbol":"AC138915.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32460266,"end":32460362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237026.1","gene_symbol":"AC104073.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65235790,"end":65236723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123352.17","gene_symbol":"SPATS2","gene_name":"spermatogenesis associated serine rich 2 [Source:HGNC Symbol;Acc:HGNC:18650]","synonyms":"SPATA10,SCR59,FLJ13117","biotype":"protein_coding","ncbi_id":"65244","summary":null,"start":49366584,"end":49527424,"strand":1,"description":"spermatogenesis associated serine rich 2 [Source:HGNC Symbol;Acc:HGNC:18650]"}, {"versioned_ensembl_gene_id":"ENSG00000108381.10","gene_symbol":"ASPA","gene_name":"aspartoacylase [Source:HGNC Symbol;Acc:HGNC:756]","synonyms":"ASP,ACY2","biotype":"protein_coding","ncbi_id":"443","summary":"This gene encodes an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate. NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter. This protein is an NAA scavenger in other tissues. Mutations in this gene cause Canavan disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]","start":3472374,"end":3503419,"strand":1,"description":"aspartoacylase [Source:HGNC Symbol;Acc:HGNC:756]"}, {"versioned_ensembl_gene_id":"ENSG00000196338.12","gene_symbol":"NLGN3","gene_name":"neuroligin 3 [Source:HGNC Symbol;Acc:HGNC:14289]","synonyms":"KIAA1480,HNL3,AUTSX1,ASPGX1","biotype":"protein_coding","ncbi_id":"54413","summary":"This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. Mutations in this gene may be associated with autism and Asperger syndrome. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Oct 2009]","start":71144831,"end":71171201,"strand":1,"description":"neuroligin 3 [Source:HGNC Symbol;Acc:HGNC:14289]"}, {"versioned_ensembl_gene_id":"ENSG00000257464.1","gene_symbol":"AC125611.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49442424,"end":49442652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236663.1","gene_symbol":"FRGCA","gene_name":"FOXM1-regulated, gastric cancer associated [Source:HGNC Symbol;Acc:HGNC:51844]","synonyms":"LncRNA-AP001631.9","biotype":"antisense_RNA","ncbi_id":"106481742","summary":null,"start":43140523,"end":43141092,"strand":-1,"description":"FOXM1-regulated, gastric cancer associated [Source:HGNC Symbol;Acc:HGNC:51844]"}, {"versioned_ensembl_gene_id":"ENSG00000213307.4","gene_symbol":"AC067863.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78661047,"end":78661576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263884.1","gene_symbol":"AP000845.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":268148,"end":270278,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125871.13","gene_symbol":"MGME1","gene_name":"mitochondrial genome maintenance exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:16205]","synonyms":"DDK1,C20orf72,bA504H3.4","biotype":"protein_coding","ncbi_id":"92667","summary":"The protein encoded by this gene is a nuclear-encoded mitochondrial protein necessary for the maintenance of mitochondrial genome synthesis. The encoded protein is a RecB-type exonuclease and primarily cleaves single-stranded DNA. Defects in this gene have been associated with mitochondrial DNA depletion syndrome-11. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]","start":17968913,"end":17991122,"strand":1,"description":"mitochondrial genome maintenance exonuclease 1 [Source:HGNC Symbol;Acc:HGNC:16205]"}, {"versioned_ensembl_gene_id":"ENSG00000271784.1","gene_symbol":"AL031055.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46689659,"end":46690289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178878.12","gene_symbol":"APOLD1","gene_name":"apolipoprotein L domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25268]","synonyms":"FLJ25138,DKFZP434F0318","biotype":"protein_coding","ncbi_id":"81575","summary":"APOLD1 is an endothelial cell early response protein that may play a role in regulation of endothelial cell signaling and vascular function (Regard et al., 2004 [PubMed 15102925]).[supplied by OMIM, Dec 2008]","start":12725917,"end":12829975,"strand":1,"description":"apolipoprotein L domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25268]"}, {"versioned_ensembl_gene_id":"ENSG00000277358.1","gene_symbol":"AL138693.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45124015,"end":45124143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227644.2","gene_symbol":"HIGD1AP11","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:43006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874453","summary":null,"start":53073110,"end":53073389,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:43006]"}, {"versioned_ensembl_gene_id":"ENSG00000147535.16","gene_symbol":"PLPP5","gene_name":"phospholipid phosphatase 5 [Source:HGNC Symbol;Acc:HGNC:25026]","synonyms":"PPAPDC1B,HTPAP,DPPL1","biotype":"protein_coding","ncbi_id":"84513","summary":null,"start":38263130,"end":38269243,"strand":-1,"description":"phospholipid phosphatase 5 [Source:HGNC Symbol;Acc:HGNC:25026]"}, {"versioned_ensembl_gene_id":"ENSG00000118231.4","gene_symbol":"CRYGD","gene_name":"crystallin gamma D [Source:HGNC Symbol;Acc:HGNC:2411]","synonyms":"CRYG4","biotype":"protein_coding","ncbi_id":"1421","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. Four gamma-crystallin genes (gamma-A through gamma-D) and three pseudogenes (gamma-E, gamma-F, gamma-G) are tandemly organized in a genomic segment as a gene cluster. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation. [provided by RefSeq, Jul 2008]","start":208121607,"end":208124501,"strand":-1,"description":"crystallin gamma D [Source:HGNC Symbol;Acc:HGNC:2411]"}, {"versioned_ensembl_gene_id":"ENSG00000274101.2","gene_symbol":"CU234142.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54575908,"end":54581617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281847.2","gene_symbol":"AL110118.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":93184973,"end":93218586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214212.8","gene_symbol":"C19orf38","gene_name":"chromosome 19 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:34073]","synonyms":"HIDE1","biotype":"protein_coding","ncbi_id":"255809","summary":null,"start":10836575,"end":10869790,"strand":1,"description":"chromosome 19 open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:34073]"}, {"versioned_ensembl_gene_id":"ENSG00000238203.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"G7c,C6orf27,NG37","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31832609,"end":31844312,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000229170.6","gene_symbol":"CR847861.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30843303,"end":30875311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234826.1","gene_symbol":"AC003084.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117998858,"end":118004045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228762.5","gene_symbol":"HCG20","gene_name":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]","synonyms":"AB023051.1,NCRNA00149","biotype":"processed_transcript","ncbi_id":"105375013","summary":null,"start":30811474,"end":30836899,"strand":1,"description":"HLA complex group 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31334]"}, {"versioned_ensembl_gene_id":"ENSG00000213937.3","gene_symbol":"CLDN9","gene_name":"claudin 9 [Source:HGNC Symbol;Acc:HGNC:2051]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9080","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This protein is one of the entry cofactors for hepatitis C virus. Mouse studies revealed that this gene is required for the preservation of sensory cells in the hearing organ and the gene deficiency is associated with deafness. [provided by RefSeq, Jun 2010]","start":3012456,"end":3014505,"strand":1,"description":"claudin 9 [Source:HGNC Symbol;Acc:HGNC:2051]"}, {"versioned_ensembl_gene_id":"ENSG00000111262.5","gene_symbol":"KCNA1","gene_name":"potassium voltage-gated channel subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:6218]","synonyms":"RBK1,MBK1,Kv1.1,HUK1,AEMK","biotype":"protein_coding","ncbi_id":"3736","summary":"This gene encodes a voltage-gated delayed potassium channel that is phylogenetically related to the Drosophila Shaker channel. The encoded protein has six putative transmembrane segments (S1-S6), and the loop between S5 and S6 forms the pore and contains the conserved selectivity filter motif (GYGD). The functional channel is a homotetramer. The N-terminus of the channel is associated with beta subunits that can modify the inactivation properties of the channel as well as affect expression levels. The C-terminus of the channel is complexed to a PDZ domain protein that is responsible for channel targeting. Mutations in this gene have been associated with myokymia with periodic ataxia (AEMK). [provided by RefSeq, Jul 2008]","start":4909893,"end":4918256,"strand":1,"description":"potassium voltage-gated channel subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:6218]"}, {"versioned_ensembl_gene_id":"ENSG00000119986.6","gene_symbol":"AVPI1","gene_name":"arginine vasopressin induced 1 [Source:HGNC Symbol;Acc:HGNC:30898]","synonyms":"VIT32,VIP32,PP5395","biotype":"protein_coding","ncbi_id":"60370","summary":null,"start":97677424,"end":97687323,"strand":-1,"description":"arginine vasopressin induced 1 [Source:HGNC Symbol;Acc:HGNC:30898]"}, {"versioned_ensembl_gene_id":"ENSG00000272518.1","gene_symbol":"AC036214.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79956465,"end":79957381,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272783.1","gene_symbol":"AC147067.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1550284,"end":1550572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249378.5","gene_symbol":"LINC01060","gene_name":"long intergenic non-protein coding RNA 1060 [Source:HGNC Symbol;Acc:HGNC:49081]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401164","summary":null,"start":188400736,"end":188681051,"strand":1,"description":"long intergenic non-protein coding RNA 1060 [Source:HGNC Symbol;Acc:HGNC:49081]"}, {"versioned_ensembl_gene_id":"ENSG00000153179.12","gene_symbol":"RASSF3","gene_name":"Ras association domain family member 3 [Source:HGNC Symbol;Acc:HGNC:14271]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283349","summary":"The RAS oncogene (MIM 190020) is mutated in nearly one-third of all human cancers. Members of the RAS superfamily are plasma membrane GTP-binding proteins that modulate intracellular signal transduction pathways. A subfamily of RAS effectors, including RASSF3, share a RAS association (RA) domain.[supplied by OMIM, Jul 2003]","start":64507001,"end":64697567,"strand":1,"description":"Ras association domain family member 3 [Source:HGNC Symbol;Acc:HGNC:14271]"}, {"versioned_ensembl_gene_id":"ENSG00000236056.1","gene_symbol":"GAPDHP14","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:4160]","synonyms":"GAPDP14","biotype":"processed_pseudogene","ncbi_id":"54050","summary":null,"start":29222321,"end":29223257,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:4160]"}, {"versioned_ensembl_gene_id":"ENSG00000256314.1","gene_symbol":"AC078962.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64654060,"end":64655019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156876.9","gene_symbol":"SASS6","gene_name":"SAS-6 centriolar assembly protein [Source:HGNC Symbol;Acc:HGNC:25403]","synonyms":"SAS6,SAS-6,FLJ22097,DKFZp761A078","biotype":"protein_coding","ncbi_id":"163786","summary":"The protein encoded by this gene is a central component of centrioles and is necessary for their duplication and function. Centrioles adopt a cartwheel-shaped structure, with the encoded protein forming the hub and spokes inside a microtubule cylinder. Defects in this gene are a cause of autosomal recessive primary microcephaly. [provided by RefSeq, Oct 2016]","start":100083563,"end":100132955,"strand":-1,"description":"SAS-6 centriolar assembly protein [Source:HGNC Symbol;Acc:HGNC:25403]"}, {"versioned_ensembl_gene_id":"ENSG00000262994.1","gene_symbol":"AC217323.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153734523,"end":153735546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148450.12","gene_symbol":"MSRB2","gene_name":"methionine sulfoxide reductase B2 [Source:HGNC Symbol;Acc:HGNC:17061]","synonyms":"MSRB,CGI-131,CBS1,CBS-1,PILB","biotype":"protein_coding","ncbi_id":"22921","summary":null,"start":23095506,"end":23122013,"strand":1,"description":"methionine sulfoxide reductase B2 [Source:HGNC Symbol;Acc:HGNC:17061]"}, {"versioned_ensembl_gene_id":"ENSG00000233950.1","gene_symbol":"AL662857.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29220658,"end":29263772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234449.2","gene_symbol":"FAM239A","gene_name":"family with sequence similarity 239 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53414]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3853010,"end":3882317,"strand":-1,"description":"family with sequence similarity 239 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53414]"}, {"versioned_ensembl_gene_id":"ENSG00000254165.1","gene_symbol":"AC090739.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42537529,"end":42538304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188352.12","gene_symbol":"FOCAD","gene_name":"focadhesin [Source:HGNC Symbol;Acc:HGNC:23377]","synonyms":"KIAA1797,FLJ20375","biotype":"protein_coding","ncbi_id":"54914","summary":null,"start":20658309,"end":20995955,"strand":1,"description":"focadhesin [Source:HGNC Symbol;Acc:HGNC:23377]"}, {"versioned_ensembl_gene_id":"ENSG00000232993.1","gene_symbol":"AL445183.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53069938,"end":53085502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153339.13","gene_symbol":"TRAPPC8","gene_name":"trafficking protein particle complex 8 [Source:HGNC Symbol;Acc:HGNC:29169]","synonyms":"TRS85,KIAA1012,HsT2706,GSG1","biotype":"protein_coding","ncbi_id":"22878","summary":null,"start":31829173,"end":31953136,"strand":-1,"description":"trafficking protein particle complex 8 [Source:HGNC Symbol;Acc:HGNC:29169]"}, {"versioned_ensembl_gene_id":"ENSG00000231064.7","gene_symbol":"AC234582.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":155195004,"end":155205495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171189.17","gene_symbol":"GRIK1","gene_name":"glutamate ionotropic receptor kainate type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4579]","synonyms":"GLUR5,GluK1","biotype":"protein_coding","ncbi_id":"2897","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. The subunit encoded by this gene is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to alter the properties of ion flow. Alternative splicing, resulting in transcript variants encoding different isoforms, has been noted for this gene. [provided by RefSeq, Jul 2008]","start":29536933,"end":29940033,"strand":-1,"description":"glutamate ionotropic receptor kainate type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4579]"}, {"versioned_ensembl_gene_id":"ENSG00000215284.2","gene_symbol":"AL512633.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46725164,"end":46725818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137965.10","gene_symbol":"IFI44","gene_name":"interferon induced protein 44 [Source:HGNC Symbol;Acc:HGNC:16938]","synonyms":"TLDC5,p44,MTAP44","biotype":"protein_coding","ncbi_id":"10561","summary":null,"start":78649796,"end":78664078,"strand":1,"description":"interferon induced protein 44 [Source:HGNC Symbol;Acc:HGNC:16938]"}, {"versioned_ensembl_gene_id":"ENSG00000121853.3","gene_symbol":"GHSR","gene_name":"growth hormone secretagogue receptor [Source:HGNC Symbol;Acc:HGNC:4267]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2693","summary":"This gene encodes a member of the G-protein coupled receptor family. The encoded protein may play a role in energy homeostasis and regulation of body weight. Two identified transcript variants are expressed in several tissues and are evolutionary conserved in fish and swine. One transcript, 1a, excises an intron and encodes the functional protein; this protein is the receptor for the Ghrelin ligand and defines a neuroendocrine pathway for growth hormone release. The second transcript (1b) retains the intron and does not function as a receptor for Ghrelin; however, it may function to attenuate activity of isoform 1a. Mutations in this gene are associated with autosomal idiopathic short stature.[provided by RefSeq, Apr 2010]","start":172445133,"end":172448456,"strand":-1,"description":"growth hormone secretagogue receptor [Source:HGNC Symbol;Acc:HGNC:4267]"}, {"versioned_ensembl_gene_id":"ENSG00000185904.11","gene_symbol":"LINC00839","gene_name":"long intergenic non-protein coding RNA 839 [Source:HGNC Symbol;Acc:HGNC:28269]","synonyms":null,"biotype":"lincRNA","ncbi_id":"84856","summary":null,"start":42475543,"end":42495336,"strand":1,"description":"long intergenic non-protein coding RNA 839 [Source:HGNC Symbol;Acc:HGNC:28269]"}, {"versioned_ensembl_gene_id":"ENSG00000158764.6","gene_symbol":"ITLN2","gene_name":"intelectin 2 [Source:HGNC Symbol;Acc:HGNC:20599]","synonyms":"HL-2","biotype":"protein_coding","ncbi_id":"142683","summary":null,"start":160945025,"end":160954799,"strand":-1,"description":"intelectin 2 [Source:HGNC Symbol;Acc:HGNC:20599]"}, {"versioned_ensembl_gene_id":"ENSG00000223376.3","gene_symbol":"CR759768.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29489052,"end":29489457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279406.1","gene_symbol":"AL359183.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":71364243,"end":71366374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130119.15","gene_symbol":"GNL3L","gene_name":"G protein nucleolar 3 like [Source:HGNC Symbol;Acc:HGNC:25553]","synonyms":"GNL3B,FLJ10613","biotype":"protein_coding","ncbi_id":"54552","summary":"The protein encoded by this gene appears to be a nucleolar GTPase that is essential for ribosomal pre-rRNA processing and cell proliferation. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]","start":54530211,"end":54561071,"strand":1,"description":"G protein nucleolar 3 like [Source:HGNC Symbol;Acc:HGNC:25553]"}, {"versioned_ensembl_gene_id":"ENSG00000258331.1","gene_symbol":"LINC02461","gene_name":"long intergenic non-protein coding RNA 2461 [Source:HGNC Symbol;Acc:HGNC:53398]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369740","summary":null,"start":43155315,"end":43163110,"strand":1,"description":"long intergenic non-protein coding RNA 2461 [Source:HGNC Symbol;Acc:HGNC:53398]"}, {"versioned_ensembl_gene_id":"ENSG00000272138.1","gene_symbol":"LINC01607","gene_name":"long intergenic non-protein coding RNA 1607 [Source:HGNC Symbol;Acc:HGNC:51660]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927067","summary":null,"start":79768142,"end":79802842,"strand":1,"description":"long intergenic non-protein coding RNA 1607 [Source:HGNC Symbol;Acc:HGNC:51660]"}, {"versioned_ensembl_gene_id":"ENSG00000211642.3","gene_symbol":"IGLV10-54","gene_name":"immunoglobulin lambda variable 10-54 [Source:HGNC Symbol;Acc:HGNC:5884]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28772","summary":null,"start":22038643,"end":22215270,"strand":1,"description":"immunoglobulin lambda variable 10-54 [Source:HGNC Symbol;Acc:HGNC:5884]"}, {"versioned_ensembl_gene_id":"ENSG00000253239.1","gene_symbol":"IGLVI-70","gene_name":"immunoglobulin lambda variable (I)-70 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5940]","synonyms":"IGLV(I)-70","biotype":"IG_V_pseudogene","ncbi_id":"28763","summary":null,"start":22026076,"end":22026593,"strand":1,"description":"immunoglobulin lambda variable (I)-70 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5940]"}, {"versioned_ensembl_gene_id":"ENSG00000224406.5","gene_symbol":"LINC02052","gene_name":"long intergenic non-protein coding RNA 2052 [Source:HGNC Symbol;Acc:HGNC:27372]","synonyms":null,"biotype":"lincRNA","ncbi_id":"253573","summary":null,"start":186454982,"end":186493661,"strand":-1,"description":"long intergenic non-protein coding RNA 2052 [Source:HGNC Symbol;Acc:HGNC:27372]"}, {"versioned_ensembl_gene_id":"ENSG00000225643.1","gene_symbol":"AL606491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25581478,"end":25590356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229014.3","gene_symbol":"RPL30P13","gene_name":"ribosomal protein L30 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271305","summary":null,"start":40068243,"end":40068590,"strand":-1,"description":"ribosomal protein L30 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36280]"}, {"versioned_ensembl_gene_id":"ENSG00000157978.11","gene_symbol":"LDLRAP1","gene_name":"low density lipoprotein receptor adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:18640]","synonyms":"MGC34705,FHCB2,FHCB1,DKFZp586D0624,ARH2,ARH","biotype":"protein_coding","ncbi_id":"26119","summary":"The protein encoded by this gene is a cytosolic protein which contains a phosphotyrosine binding (PTD) domain. The PTD domain has been found to interact with the cytoplasmic tail of the LDL receptor. Mutations in this gene lead to LDL receptor malfunction and cause the disorder autosomal recessive hypercholesterolaemia. [provided by RefSeq, Jul 2008]","start":25543580,"end":25568886,"strand":1,"description":"low density lipoprotein receptor adaptor protein 1 [Source:HGNC Symbol;Acc:HGNC:18640]"}, {"versioned_ensembl_gene_id":"ENSG00000248810.1","gene_symbol":"LINC02432","gene_name":"long intergenic non-protein coding RNA 2432 [Source:HGNC Symbol;Acc:HGNC:53363]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507639","summary":null,"start":141319450,"end":141332618,"strand":-1,"description":"long intergenic non-protein coding RNA 2432 [Source:HGNC Symbol;Acc:HGNC:53363]"}, {"versioned_ensembl_gene_id":"ENSG00000229485.1","gene_symbol":"KSR1P1","gene_name":"kinase suppressor of ras 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479050","summary":null,"start":42149310,"end":42149549,"strand":-1,"description":"kinase suppressor of ras 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44977]"}, {"versioned_ensembl_gene_id":"ENSG00000187514.16","gene_symbol":"PTMA","gene_name":"prothymosin, alpha [Source:HGNC Symbol;Acc:HGNC:9623]","synonyms":"TMSA","biotype":"protein_coding","ncbi_id":"5757","summary":null,"start":231706895,"end":231713541,"strand":1,"description":"prothymosin, alpha [Source:HGNC Symbol;Acc:HGNC:9623]"}, {"versioned_ensembl_gene_id":"ENSG00000227679.1","gene_symbol":"AL133173.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38762095,"end":38762491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254586.1","gene_symbol":"AC124301.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17695022,"end":17697471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255335.1","gene_symbol":"AC124301.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17695267,"end":17696940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115993.12","gene_symbol":"TRAK2","gene_name":"trafficking kinesin protein 2 [Source:HGNC Symbol;Acc:HGNC:13206]","synonyms":"OIP98,MILT2,KIAA0549,GRIF-1,CALS-C,ALS2CR3","biotype":"protein_coding","ncbi_id":"66008","summary":null,"start":201377207,"end":201451579,"strand":-1,"description":"trafficking kinesin protein 2 [Source:HGNC Symbol;Acc:HGNC:13206]"}, {"versioned_ensembl_gene_id":"ENSG00000173588.14","gene_symbol":"CEP83","gene_name":"centrosomal protein 83 [Source:HGNC Symbol;Acc:HGNC:17966]","synonyms":"NY-REN-58,NPHP18,CCDC41","biotype":"protein_coding","ncbi_id":"51134","summary":"The protein encoded by this gene is a centriolar protein involved in primary cilium assembly. Defects in this gene have been associated with infantile nephronophthisis and intellectual disability. [provided by RefSeq, Oct 2016]","start":94306449,"end":94459988,"strand":-1,"description":"centrosomal protein 83 [Source:HGNC Symbol;Acc:HGNC:17966]"}, {"versioned_ensembl_gene_id":"ENSG00000234541.2","gene_symbol":"CHEK2P5","gene_name":"checkpoint kinase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43581]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479022","summary":null,"start":38713195,"end":38719229,"strand":1,"description":"checkpoint kinase 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43581]"}, {"versioned_ensembl_gene_id":"ENSG00000184949.15","gene_symbol":"FAM227A","gene_name":"family with sequence similarity 227 member A [Source:HGNC Symbol;Acc:HGNC:44197]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646851","summary":null,"start":38578120,"end":38656629,"strand":-1,"description":"family with sequence similarity 227 member A [Source:HGNC Symbol;Acc:HGNC:44197]"}, {"versioned_ensembl_gene_id":"ENSG00000161912.17","gene_symbol":"ADCY10P1","gene_name":"adenylate cyclase 10, soluble pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44143]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"221442","summary":null,"start":41101022,"end":41140835,"strand":1,"description":"adenylate cyclase 10, soluble pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44143]"}, {"versioned_ensembl_gene_id":"ENSG00000196872.11","gene_symbol":"KIAA1211L","gene_name":"KIAA1211 like [Source:HGNC Symbol;Acc:HGNC:33454]","synonyms":"MGC42367,C2orf55","biotype":"protein_coding","ncbi_id":"343990","summary":null,"start":98793846,"end":98936259,"strand":-1,"description":"KIAA1211 like [Source:HGNC Symbol;Acc:HGNC:33454]"}, {"versioned_ensembl_gene_id":"ENSG00000177673.3","gene_symbol":"TEX44","gene_name":"testis expressed 44 [Source:HGNC Symbol;Acc:HGNC:28563]","synonyms":"MGC35154,C2orf57","biotype":"protein_coding","ncbi_id":"165100","summary":null,"start":231592901,"end":231594283,"strand":1,"description":"testis expressed 44 [Source:HGNC Symbol;Acc:HGNC:28563]"}, {"versioned_ensembl_gene_id":"ENSG00000105289.14","gene_symbol":"TJP3","gene_name":"tight junction protein 3 [Source:HGNC Symbol;Acc:HGNC:11829]","synonyms":"ZO-3","biotype":"protein_coding","ncbi_id":"27134","summary":"The protein encoded by this gene is a member of the membrane-associated guanylate kinase-like (MAGUK) protein family which is characterized by members having multiple PDZ domains, a single SH3 domain, and a single guanylate kinase-like (GUK)-domain. In addition, members of the zonula occludens protein subfamily have an acidic domain, a basic arginine-rich region, and a proline-rich domain. The protein encoded by this gene plays a role in the linkage between the actin cytoskeleton and tight-junctions and also sequesters cyclin D1 at tight junctions during mitosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. This gene has a partial pseudogene on chromosome 1. [provided by RefSeq, May 2012]","start":3708109,"end":3750813,"strand":1,"description":"tight junction protein 3 [Source:HGNC Symbol;Acc:HGNC:11829]"}, {"versioned_ensembl_gene_id":"ENSG00000276307.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000267138.1","gene_symbol":"AC005954.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3754620,"end":3756659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280081.3","gene_symbol":"LINC01667","gene_name":"long intergenic non-protein coding RNA 1667 [Source:HGNC Symbol;Acc:HGNC:52455]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441058","summary":null,"start":9781918,"end":9814009,"strand":-1,"description":"long intergenic non-protein coding RNA 1667 [Source:HGNC Symbol;Acc:HGNC:52455]"}, {"versioned_ensembl_gene_id":"ENSG00000250939.2","gene_symbol":"AC034198.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12850659,"end":12850860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277481.1","gene_symbol":"PKD1L3","gene_name":"polycystin 1 like 3, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:21716]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342372","summary":"This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores.[provided by RefSeq, Apr 2009]","start":71929538,"end":71999978,"strand":-1,"description":"polycystin 1 like 3, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:21716]"}, {"versioned_ensembl_gene_id":"ENSG00000164975.15","gene_symbol":"SNAPC3","gene_name":"small nuclear RNA activating complex polypeptide 3 [Source:HGNC Symbol;Acc:HGNC:11136]","synonyms":"SNAP50,PTFbeta,MGC33124,MGC132011","biotype":"protein_coding","ncbi_id":"6619","summary":null,"start":15422704,"end":15465953,"strand":1,"description":"small nuclear RNA activating complex polypeptide 3 [Source:HGNC Symbol;Acc:HGNC:11136]"}, {"versioned_ensembl_gene_id":"ENSG00000101557.14","gene_symbol":"USP14","gene_name":"ubiquitin specific peptidase 14 [Source:HGNC Symbol;Acc:HGNC:12612]","synonyms":"TGT","biotype":"protein_coding","ncbi_id":"9097","summary":"This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. Mice with a mutation that results in reduced expression of the ortholog of this protein are retarded for growth, develop severe tremors by 2 to 3 weeks of age followed by hindlimb paralysis and death by 6 to 10 weeks of age. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":158383,"end":214629,"strand":1,"description":"ubiquitin specific peptidase 14 [Source:HGNC Symbol;Acc:HGNC:12612]"}, {"versioned_ensembl_gene_id":"ENSG00000236727.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30478618,"end":30483222,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000214021.15","gene_symbol":"TTLL3","gene_name":"tubulin tyrosine ligase like 3 [Source:HGNC Symbol;Acc:HGNC:24483]","synonyms":"HOTTL,DKFZP434B103","biotype":"protein_coding","ncbi_id":"26140","summary":null,"start":9808086,"end":9855138,"strand":1,"description":"tubulin tyrosine ligase like 3 [Source:HGNC Symbol;Acc:HGNC:24483]"}, {"versioned_ensembl_gene_id":"ENSG00000235656.1","gene_symbol":"RPL36P18","gene_name":"ribosomal protein L36 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36856]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271394","summary":null,"start":115198432,"end":115198749,"strand":1,"description":"ribosomal protein L36 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36856]"}, {"versioned_ensembl_gene_id":"ENSG00000136274.8","gene_symbol":"NACAD","gene_name":"NAC alpha domain containing [Source:HGNC Symbol;Acc:HGNC:22196]","synonyms":"KIAA0363","biotype":"protein_coding","ncbi_id":"23148","summary":null,"start":45080438,"end":45088914,"strand":-1,"description":"NAC alpha domain containing [Source:HGNC Symbol;Acc:HGNC:22196]"}, {"versioned_ensembl_gene_id":"ENSG00000275623.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"cl-6,nkat2,nkat2a,nkat2b,p58,CD158B2","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738461,"end":54752744,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000244560.6","gene_symbol":"AC004890.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149285281,"end":149297312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238087.3","gene_symbol":"FMO8P","gene_name":"flavin containing monooxygenase 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:32209]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129007","summary":null,"start":166566178,"end":166580705,"strand":1,"description":"flavin containing monooxygenase 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:32209]"}, {"versioned_ensembl_gene_id":"ENSG00000170260.8","gene_symbol":"ZNF212","gene_name":"zinc finger protein 212 [Source:HGNC Symbol;Acc:HGNC:13004]","synonyms":"C2H2-150","biotype":"protein_coding","ncbi_id":"7988","summary":"This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008]","start":149239651,"end":149255609,"strand":1,"description":"zinc finger protein 212 [Source:HGNC Symbol;Acc:HGNC:13004]"}, {"versioned_ensembl_gene_id":"ENSG00000064313.11","gene_symbol":"TAF2","gene_name":"TATA-box binding protein associated factor 2 [Source:HGNC Symbol;Acc:HGNC:11536]","synonyms":"TAFII150,TAF2B,CIF150","biotype":"protein_coding","ncbi_id":"6873","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the larger subunits of TFIID that is stably associated with the TFIID complex. It contributes to interactions at and downstream of the transcription initiation site, interactions that help determine transcription complex response to activators. [provided by RefSeq, Jul 2008]","start":119730775,"end":119832863,"strand":-1,"description":"TATA-box binding protein associated factor 2 [Source:HGNC Symbol;Acc:HGNC:11536]"}, {"versioned_ensembl_gene_id":"ENSG00000255356.2","gene_symbol":"AC007536.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7896608,"end":7896956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271664.1","gene_symbol":"AC004890.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":149275619,"end":149277992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219139.1","gene_symbol":"TYMSP1","gene_name":"thymidylate synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419610","summary":null,"start":96653274,"end":96654142,"strand":1,"description":"thymidylate synthetase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52351]"}, {"versioned_ensembl_gene_id":"ENSG00000272414.5","gene_symbol":"FAM47E-STBD1","gene_name":"FAM47E-STBD1 readthrough [Source:HGNC Symbol;Acc:HGNC:44667]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100631383","summary":"This locus represents naturally occurring read-through transcription between the neighboring FAM47E (family with sequence similarity 47, member E) and STBD1 (starch binding domain 1) genes on chromosome 4. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to frameshifts relative to the downstream gene. [provided by RefSeq, Jul 2011]","start":76251721,"end":76311129,"strand":1,"description":"FAM47E-STBD1 readthrough [Source:HGNC Symbol;Acc:HGNC:44667]"}, {"versioned_ensembl_gene_id":"ENSG00000130224.14","gene_symbol":"LRCH2","gene_name":"leucine rich repeats and calponin homology domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29292]","synonyms":"KIAA1495","biotype":"protein_coding","ncbi_id":"57631","summary":"This gene encodes a member of the leucine-rich repeat and calponin homology domain-containing protein family. These family members contain multiple N-terminal leucine-rich repeats, in addition to a C-terminal calponin homology domain, a type of domain that mediates interactions with actin filaments. These proteins are conserved across animal species, and studies of a similar Drosophila protein indicate a function as a cytoskeletal scaffolding protein. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":115110616,"end":115234072,"strand":-1,"description":"leucine rich repeats and calponin homology domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29292]"}, {"versioned_ensembl_gene_id":"ENSG00000204946.9","gene_symbol":"ZNF783","gene_name":"zinc finger family member 783 [Source:HGNC Symbol;Acc:HGNC:27222]","synonyms":"DKFZp667J212","biotype":"protein_coding","ncbi_id":"100289678","summary":null,"start":149262171,"end":149297302,"strand":1,"description":"zinc finger family member 783 [Source:HGNC Symbol;Acc:HGNC:27222]"}, {"versioned_ensembl_gene_id":"ENSG00000175718.9","gene_symbol":"RBMXL3","gene_name":"RNA binding motif protein, X-linked like 3 [Source:HGNC Symbol;Acc:HGNC:26859]","synonyms":"FLJ40249,CXorf55","biotype":"protein_coding","ncbi_id":"139804","summary":null,"start":115189427,"end":115192868,"strand":1,"description":"RNA binding motif protein, X-linked like 3 [Source:HGNC Symbol;Acc:HGNC:26859]"}, {"versioned_ensembl_gene_id":"ENSG00000189157.13","gene_symbol":"FAM47E","gene_name":"family with sequence similarity 47 member E [Source:HGNC Symbol;Acc:HGNC:34343]","synonyms":"FLJ42946,LOC100129583","biotype":"protein_coding","ncbi_id":"100129583","summary":null,"start":76214040,"end":76283780,"strand":1,"description":"family with sequence similarity 47 member E [Source:HGNC Symbol;Acc:HGNC:34343]"}, {"versioned_ensembl_gene_id":"ENSG00000135679.22","gene_symbol":"MDM2","gene_name":"MDM2 proto-oncogene [Source:HGNC Symbol;Acc:HGNC:6973]","synonyms":"HDM2,MGC5370","biotype":"protein_coding","ncbi_id":"4193","summary":"This gene encodes a nuclear-localized E3 ubiquitin ligase. The encoded protein can promote tumor formation by targeting tumor suppressor proteins, such as p53, for proteasomal degradation. This gene is itself transcriptionally-regulated by p53. Overexpression or amplification of this locus is detected in a variety of different cancers. There is a pseudogene for this gene on chromosome 2. Alternative splicing results in a multitude of transcript variants, many of which may be expressed only in tumor cells. [provided by RefSeq, Jun 2013]","start":68808176,"end":68850686,"strand":1,"description":"MDM2 proto-oncogene [Source:HGNC Symbol;Acc:HGNC:6973]"}, {"versioned_ensembl_gene_id":"ENSG00000163754.17","gene_symbol":"GYG1","gene_name":"glycogenin 1 [Source:HGNC Symbol;Acc:HGNC:4699]","synonyms":"GYG","biotype":"protein_coding","ncbi_id":"2992","summary":"This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]","start":148991341,"end":149027668,"strand":1,"description":"glycogenin 1 [Source:HGNC Symbol;Acc:HGNC:4699]"}, {"versioned_ensembl_gene_id":"ENSG00000251669.5","gene_symbol":"FAM86EP","gene_name":"family with sequence similarity 86 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:28017]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"348926","summary":null,"start":3941760,"end":3955419,"strand":-1,"description":"family with sequence similarity 86 member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:28017]"}, {"versioned_ensembl_gene_id":"ENSG00000253917.4","gene_symbol":"AC226119.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":3915183,"end":3955419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271977.1","gene_symbol":"AC226119.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3915187,"end":3924274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167306.19","gene_symbol":"MYO5B","gene_name":"myosin VB [Source:HGNC Symbol;Acc:HGNC:7603]","synonyms":"KIAA1119","biotype":"protein_coding","ncbi_id":"4645","summary":"The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009]","start":49822813,"end":50195093,"strand":-1,"description":"myosin VB [Source:HGNC Symbol;Acc:HGNC:7603]"}, {"versioned_ensembl_gene_id":"ENSG00000157450.15","gene_symbol":"RNF111","gene_name":"ring finger protein 111 [Source:HGNC Symbol;Acc:HGNC:17384]","synonyms":"FLJ38008,DKFZP761D081,Arkadia,ARK","biotype":"protein_coding","ncbi_id":"54778","summary":"The protein encoded by this gene is a nuclear RING-domain containing E3 ubiquitin ligase. This protein interacts with the transforming growth factor (TGF) -beta/NODAL signaling pathway by promoting the ubiquitination and proteosomal degradation of negative regulators, like SMAD proteins, and thereby enhances TGF-beta target-gene transcription. As a modulator of the nodal signaling cascade, this gene plays a critical role in the induction of mesoderm during embryonic development. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012]","start":58865175,"end":59097419,"strand":1,"description":"ring finger protein 111 [Source:HGNC Symbol;Acc:HGNC:17384]"}, {"versioned_ensembl_gene_id":"ENSG00000225798.1","gene_symbol":"AC025918.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58889967,"end":58894082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267196.1","gene_symbol":"AC091044.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49969721,"end":49970957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254204.1","gene_symbol":"AC022034.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53515170,"end":53515905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253369.1","gene_symbol":"AC131902.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53395211,"end":53395946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274295.1","gene_symbol":"AC131902.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53394215,"end":53394795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101782.14","gene_symbol":"RIOK3","gene_name":"RIO kinase 3 [Source:HGNC Symbol;Acc:HGNC:11451]","synonyms":"SUDD","biotype":"protein_coding","ncbi_id":"8780","summary":"This gene was first identified by the similarity of its product to the Aspergillus nidulans SUDD protein. This gene is now recognized as a member of the right open reading frame (RIO) kinase gene family. This gene encodes a serine/threonine kinase that localizes to the cytoplasm and plays a role in the processing of the pre-40 S ribosomal subunit. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2017]","start":23452823,"end":23486603,"strand":1,"description":"RIO kinase 3 [Source:HGNC Symbol;Acc:HGNC:11451]"}, {"versioned_ensembl_gene_id":"ENSG00000240224.1","gene_symbol":"UGT1A5","gene_name":"UDP glucuronosyltransferase family 1 member A5 [Source:HGNC Symbol;Acc:HGNC:12537]","synonyms":"UGT1E","biotype":"protein_coding","ncbi_id":"54579","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. [provided by RefSeq, Jul 2008]","start":233712992,"end":233773299,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A5 [Source:HGNC Symbol;Acc:HGNC:12537]"}, {"versioned_ensembl_gene_id":"ENSG00000250829.2","gene_symbol":"AC108865.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186890969,"end":186892366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272218.1","gene_symbol":"AC108865.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186892552,"end":186892983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249539.1","gene_symbol":"MRPS36P2","gene_name":"mitochondrial ribosomal protein S36 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347706","summary":null,"start":186900540,"end":186900838,"strand":1,"description":"mitochondrial ribosomal protein S36 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29772]"}, {"versioned_ensembl_gene_id":"ENSG00000249742.1","gene_symbol":"AC110772.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186979490,"end":187021973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250971.1","gene_symbol":"AC108474.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187060099,"end":187060930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249747.1","gene_symbol":"LINC02374","gene_name":"long intergenic non-protein coding RNA 2374 [Source:HGNC Symbol;Acc:HGNC:53296]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377600","summary":null,"start":187201986,"end":187209346,"strand":1,"description":"long intergenic non-protein coding RNA 2374 [Source:HGNC Symbol;Acc:HGNC:53296]"}, {"versioned_ensembl_gene_id":"ENSG00000282698.1","gene_symbol":"RPL3P10","gene_name":"ribosomal protein L3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36819]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129004","summary":null,"start":39157538,"end":39158701,"strand":-1,"description":"ribosomal protein L3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36819]"}, {"versioned_ensembl_gene_id":"ENSG00000109180.14","gene_symbol":"OCIAD1","gene_name":"OCIA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16074]","synonyms":"FLJ20455,Asrij,TPA018,OCIA","biotype":"protein_coding","ncbi_id":"54940","summary":null,"start":48805212,"end":48861817,"strand":1,"description":"OCIA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16074]"}, {"versioned_ensembl_gene_id":"ENSG00000124596.16","gene_symbol":"OARD1","gene_name":"O-acyl-ADP-ribose deacylase 1 [Source:HGNC Symbol;Acc:HGNC:21257]","synonyms":"TARG1,MGC19570,dJ34B21.3,C6orf130","biotype":"protein_coding","ncbi_id":"221443","summary":"The protein encoded by this gene is a deacylase that can convert O-acetyl-ADP-ribose to ADP-ribose and acetate, O-propionyl-ADP-ribose to ADP-ribose and propionate, and O-butyryl-ADP-ribose to ADP-ribose and butyrate. The ADP-ribose product is able to inhibit these reactions through a competitive feedback loop. [provided by RefSeq, Jul 2016]","start":41033627,"end":41097787,"strand":-1,"description":"O-acyl-ADP-ribose deacylase 1 [Source:HGNC Symbol;Acc:HGNC:21257]"}, {"versioned_ensembl_gene_id":"ENSG00000259519.1","gene_symbol":"AC051619.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45170344,"end":45199958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137857.17","gene_symbol":"DUOX1","gene_name":"dual oxidase 1 [Source:HGNC Symbol;Acc:HGNC:3062]","synonyms":"THOX1,NOXEF1,LNOX1","biotype":"protein_coding","ncbi_id":"53905","summary":"The protein encoded by this gene is a glycoprotein and a member of the NADPH oxidase family. The synthesis of thyroid hormone is catalyzed by a protein complex located at the apical membrane of thyroid follicular cells. This complex contains an iodide transporter, thyroperoxidase, and a peroxide generating system that includes proteins encoded by this gene and the similar DUOX2 gene. This protein is known as dual oxidase because it has both a peroxidase homology domain and a gp91phox domain. This protein generates hydrogen peroxide and thereby plays a role in the activity of thyroid peroxidase, lactoperoxidase, and in lactoperoxidase-mediated antimicrobial defense at mucosal surfaces. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2012]","start":45129933,"end":45165576,"strand":1,"description":"dual oxidase 1 [Source:HGNC Symbol;Acc:HGNC:3062]"}, {"versioned_ensembl_gene_id":"ENSG00000257303.1","gene_symbol":"AC073896.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56300142,"end":56314808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102984.14","gene_symbol":"ZNF821","gene_name":"zinc finger protein 821 [Source:HGNC Symbol;Acc:HGNC:28043]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55565","summary":"This gene encodes a protein with two C2H2 zinc finger motifs and a score-and-three (23)-amino acid peptide repeat (STPR) domain. The STPR domain of the encoded protein binds to double stranded DNA and may also contain a nuclear localization signal, suggesting that this protein interacts with chromosomal DNA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":71859680,"end":71895336,"strand":-1,"description":"zinc finger protein 821 [Source:HGNC Symbol;Acc:HGNC:28043]"}, {"versioned_ensembl_gene_id":"ENSG00000163472.18","gene_symbol":"TMEM79","gene_name":"transmembrane protein 79 [Source:HGNC Symbol;Acc:HGNC:28196]","synonyms":"MGC13102,MATT,FLJ32254,FLJ16057","biotype":"protein_coding","ncbi_id":"84283","summary":null,"start":156282935,"end":156293185,"strand":1,"description":"transmembrane protein 79 [Source:HGNC Symbol;Acc:HGNC:28196]"}, {"versioned_ensembl_gene_id":"ENSG00000236648.1","gene_symbol":"AL136529.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17717687,"end":17749978,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079134.11","gene_symbol":"THOC1","gene_name":"THO complex 1 [Source:HGNC Symbol;Acc:HGNC:19070]","synonyms":"P84,HPR1","biotype":"protein_coding","ncbi_id":"9984","summary":"HPR1 is part of the TREX (transcription/export) complex, which includes TEX1 (MIM 606929), THO2 (MIM 300395), ALY (MIM 604171), and UAP56 (MIM 142560).[supplied by OMIM, Nov 2010]","start":214520,"end":268050,"strand":-1,"description":"THO complex 1 [Source:HGNC Symbol;Acc:HGNC:19070]"}, {"versioned_ensembl_gene_id":"ENSG00000117148.7","gene_symbol":"ACTL8","gene_name":"actin like 8 [Source:HGNC Symbol;Acc:HGNC:24018]","synonyms":"CT57","biotype":"protein_coding","ncbi_id":"81569","summary":null,"start":17755313,"end":17827063,"strand":1,"description":"actin like 8 [Source:HGNC Symbol;Acc:HGNC:24018]"}, {"versioned_ensembl_gene_id":"ENSG00000062485.18","gene_symbol":"CS","gene_name":"citrate synthase [Source:HGNC Symbol;Acc:HGNC:2422]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1431","summary":"The protein encoded by this gene is a Krebs tricarboxylic acid cycle enzyme that catalyzes the synthesis of citrate from oxaloacetate and acetyl coenzyme A. The enzyme is found in nearly all cells capable of oxidative metablism. This protein is nuclear encoded and transported into the mitochondrial matrix, where the mature form is found. [provided by RefSeq, Jul 2008]","start":56271699,"end":56300392,"strand":-1,"description":"citrate synthase [Source:HGNC Symbol;Acc:HGNC:2422]"}, {"versioned_ensembl_gene_id":"ENSG00000106603.18","gene_symbol":"COA1","gene_name":"cytochrome c oxidase assembly factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:21868]","synonyms":"MITRAC15,FLJ10803,C7orf44","biotype":"protein_coding","ncbi_id":"55744","summary":null,"start":43608456,"end":43729717,"strand":-1,"description":"cytochrome c oxidase assembly factor 1 homolog [Source:HGNC Symbol;Acc:HGNC:21868]"}, {"versioned_ensembl_gene_id":"ENSG00000230483.1","gene_symbol":"AC124057.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2404515,"end":2407908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232232.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30415319,"end":30415453,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000284653.1","gene_symbol":"AL357509.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18015712,"end":18045612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229149.1","gene_symbol":"CR759890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30423182,"end":30423815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237975.6","gene_symbol":"FLG-AS1","gene_name":"FLG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27913]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"339400","summary":null,"start":152168125,"end":152445456,"strand":1,"description":"FLG antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27913]"}, {"versioned_ensembl_gene_id":"ENSG00000070985.13","gene_symbol":"TRPM5","gene_name":"transient receptor potential cation channel subfamily M member 5 [Source:HGNC Symbol;Acc:HGNC:14323]","synonyms":"MTR1,LTRPC5","biotype":"protein_coding","ncbi_id":"29850","summary":"This gene encodes a member of the transient receptor potential (TRP) protein family, which is a diverse group of proteins with structural features typical of ion channels. This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Ca(2+) ions. It is activated by lower concentrations of intracellular Ca(2+), and inhibited by higher concentrations. It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15.5, and has been shown to be imprinted, with exclusive expression from the paternal allele. [provided by RefSeq, Oct 2010]","start":2404515,"end":2423045,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 5 [Source:HGNC Symbol;Acc:HGNC:14323]"}, {"versioned_ensembl_gene_id":"ENSG00000171456.16","gene_symbol":"ASXL1","gene_name":"additional sex combs like 1, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:18318]","synonyms":"KIAA0978","biotype":"protein_coding","ncbi_id":"171023","summary":"This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":32358344,"end":32439319,"strand":1,"description":"additional sex combs like 1, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:18318]"}, {"versioned_ensembl_gene_id":"ENSG00000198715.11","gene_symbol":"GLMP","gene_name":"glycosylated lysosomal membrane protein [Source:HGNC Symbol;Acc:HGNC:29436]","synonyms":"NCU-G1,MGC31963,C1orf85","biotype":"protein_coding","ncbi_id":"112770","summary":null,"start":156290089,"end":156295689,"strand":-1,"description":"glycosylated lysosomal membrane protein [Source:HGNC Symbol;Acc:HGNC:29436]"}, {"versioned_ensembl_gene_id":"ENSG00000256325.1","gene_symbol":"AC025423.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68828118,"end":68828553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257336.1","gene_symbol":"PRELID2P1","gene_name":"PRELI domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43892]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102606462","summary":null,"start":68957377,"end":68957677,"strand":-1,"description":"PRELI domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43892]"}, {"versioned_ensembl_gene_id":"ENSG00000257289.1","gene_symbol":"AC025423.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68913804,"end":68914022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256664.1","gene_symbol":"AC025423.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68841946,"end":68842384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000093217.9","gene_symbol":"XYLB","gene_name":"xylulokinase [Source:HGNC Symbol;Acc:HGNC:12839]","synonyms":"FLJ10343,FLJ12539","biotype":"protein_coding","ncbi_id":"9942","summary":"The protein encoded by this gene shares 22% sequence identity with Hemophilus influenzae xylulokinase, and even higher identity to other gene products in C.elegans (45%) and yeast (31-35%), which are thought to belong to a family of enzymes that include fucokinase, gluconokinase, glycerokinase and xylulokinase. These proteins play important roles in energy metabolism. [provided by RefSeq, Aug 2009]","start":38346760,"end":38421348,"strand":1,"description":"xylulokinase [Source:HGNC Symbol;Acc:HGNC:12839]"}, {"versioned_ensembl_gene_id":"ENSG00000135678.11","gene_symbol":"CPM","gene_name":"carboxypeptidase M [Source:HGNC Symbol;Acc:HGNC:2311]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1368","summary":"The protein encoded by this gene is a membrane-bound arginine/lysine carboxypeptidase. Its expression is associated with monocyte to macrophage differentiation. This encoded protein contains hydrophobic regions at the amino and carboxy termini and has 6 potential asparagine-linked glycosylation sites. The active site residues of carboxypeptidases A and B are conserved in this protein. Three alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":68842197,"end":68971570,"strand":-1,"description":"carboxypeptidase M [Source:HGNC Symbol;Acc:HGNC:2311]"}, {"versioned_ensembl_gene_id":"ENSG00000167165.18","gene_symbol":"UGT1A6","gene_name":"UDP glucuronosyltransferase family 1 member A6 [Source:HGNC Symbol;Acc:HGNC:12538]","synonyms":"UGT1F,HLUGP,GNT1","biotype":"protein_coding","ncbi_id":"54578","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene is active on phenolic and planar compounds. Alternative splicing in the unique 5' end of this gene results in two transcript variants. [provided by RefSeq, Jul 2008]","start":233691607,"end":233773300,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A6 [Source:HGNC Symbol;Acc:HGNC:12538]"}, {"versioned_ensembl_gene_id":"ENSG00000214353.7","gene_symbol":"VAC14-AS1","gene_name":"VAC14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48605]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100130894","summary":null,"start":70755098,"end":70773251,"strand":1,"description":"VAC14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48605]"}, {"versioned_ensembl_gene_id":"ENSG00000279815.1","gene_symbol":"AC020763.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70768356,"end":70768785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279123.1","gene_symbol":"AC027281.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70778433,"end":70779145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267511.1","gene_symbol":"ADAD1P2","gene_name":"adenosine deaminase domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422407","summary":null,"start":50063795,"end":50064440,"strand":1,"description":"adenosine deaminase domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44552]"}, {"versioned_ensembl_gene_id":"ENSG00000267322.2","gene_symbol":"SNHG22","gene_name":"small nucleolar RNA host gene 22 [Source:HGNC Symbol;Acc:HGNC:50285]","synonyms":"SCARNA17HG","biotype":"antisense_RNA","ncbi_id":"103091864","summary":null,"start":49814023,"end":49851059,"strand":1,"description":"small nucleolar RNA host gene 22 [Source:HGNC Symbol;Acc:HGNC:50285]"}, {"versioned_ensembl_gene_id":"ENSG00000279122.1","gene_symbol":"AC020763.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70768967,"end":70770221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256663.1","gene_symbol":"AC112777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20551590,"end":20553012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279412.1","gene_symbol":"AC020763.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70713987,"end":70716890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131982.5","gene_symbol":"UBE2L2","gene_name":"ubiquitin conjugating enzyme E2 L2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12487]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506424","summary":null,"start":20449655,"end":20450083,"strand":-1,"description":"ubiquitin conjugating enzyme E2 L2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12487]"}, {"versioned_ensembl_gene_id":"ENSG00000172572.6","gene_symbol":"PDE3A","gene_name":"phosphodiesterase 3A [Source:HGNC Symbol;Acc:HGNC:8778]","synonyms":"CGI-PDE","biotype":"protein_coding","ncbi_id":"5139","summary":"This gene encodes a member of the cGMP-inhibited cyclic nucleotide phosphodiesterase (cGI-PDE) family. cGI-PDE enzymes hydrolyze both cAMP and cGMP, and play critical roles in many cellular processes by regulating the amplitude and duration of intracellular cyclic nucleotide signals. The encoded protein mediates platelet aggregation and also plays important roles in cardiovascular function by regulating vascular smooth muscle contraction and relaxation. Inhibitors of the encoded protein may be effective in treating congestive heart failure. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":20369245,"end":20684381,"strand":1,"description":"phosphodiesterase 3A [Source:HGNC Symbol;Acc:HGNC:8778]"}, {"versioned_ensembl_gene_id":"ENSG00000267591.1","gene_symbol":"AC105224.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50098742,"end":50099162,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167315.17","gene_symbol":"ACAA2","gene_name":"acetyl-CoA acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:83]","synonyms":"DSAEC","biotype":"protein_coding","ncbi_id":"10449","summary":"The encoded protein catalyzes the last step of the mitochondrial fatty acid beta-oxidation spiral. Unlike most mitochondrial matrix proteins, it contains a non-cleavable amino-terminal targeting signal. [provided by RefSeq, Jul 2008]","start":49782167,"end":49813960,"strand":-1,"description":"acetyl-CoA acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:83]"}, {"versioned_ensembl_gene_id":"ENSG00000257579.1","gene_symbol":"AC007540.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107610034,"end":107617721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250151.9","gene_symbol":"ARPC4-TTLL3","gene_name":"ARPC4-TTLL3 readthrough [Source:HGNC Symbol;Acc:HGNC:38830]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526693","summary":"This locus represents naturally occurring read-through transcription between the neighboring ARPC4 (actin related protein 2/3 complex, subunit 4) and TTLL3 (tubulin tyrosine ligase-like family, member 3) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":9793082,"end":9835401,"strand":1,"description":"ARPC4-TTLL3 readthrough [Source:HGNC Symbol;Acc:HGNC:38830]"}, {"versioned_ensembl_gene_id":"ENSG00000151136.14","gene_symbol":"BTBD11","gene_name":"BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:23844]","synonyms":"FLJ33957,ABTB2B","biotype":"protein_coding","ncbi_id":"121551","summary":null,"start":107318413,"end":107659642,"strand":1,"description":"BTB domain containing 11 [Source:HGNC Symbol;Acc:HGNC:23844]"}, {"versioned_ensembl_gene_id":"ENSG00000213183.3","gene_symbol":"RPS7P8","gene_name":"ribosomal protein S7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35710]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442237","summary":null,"start":96648489,"end":96649069,"strand":-1,"description":"ribosomal protein S7 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35710]"}, {"versioned_ensembl_gene_id":"ENSG00000250658.1","gene_symbol":"AC097652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":187304083,"end":187309682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250042.1","gene_symbol":"LINC02514","gene_name":"long intergenic non-protein coding RNA 2514 [Source:HGNC Symbol;Acc:HGNC:53503]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377602","summary":null,"start":187370648,"end":187371921,"strand":1,"description":"long intergenic non-protein coding RNA 2514 [Source:HGNC Symbol;Acc:HGNC:53503]"}, {"versioned_ensembl_gene_id":"ENSG00000283084.1","gene_symbol":"AC026634.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23485000,"end":23485197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136698.8","gene_symbol":"CFC1","gene_name":"cripto, FRL-1, cryptic family 1 [Source:HGNC Symbol;Acc:HGNC:18292]","synonyms":"HTX2,CRYPTIC","biotype":"protein_coding","ncbi_id":"55997","summary":"This gene encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Proteins in this family share a variant EGF-like motif, a conserved cysteine-rich domain, and a C-terminal hydrophobic region. The protein encoded by this gene is necessary for patterning the left-right embryonic axis. Mutations in this gene are associated with defects in organ development, including autosomal visceral heterotaxy and congenital heart disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":130592168,"end":130599575,"strand":-1,"description":"cripto, FRL-1, cryptic family 1 [Source:HGNC Symbol;Acc:HGNC:18292]"}, {"versioned_ensembl_gene_id":"ENSG00000100258.17","gene_symbol":"LMF2","gene_name":"lipase maturation factor 2 [Source:HGNC Symbol;Acc:HGNC:25096]","synonyms":"TMEM153,TMEM112B","biotype":"protein_coding","ncbi_id":"91289","summary":null,"start":50502949,"end":50507691,"strand":-1,"description":"lipase maturation factor 2 [Source:HGNC Symbol;Acc:HGNC:25096]"}, {"versioned_ensembl_gene_id":"ENSG00000279208.1","gene_symbol":"CR381653.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9369285,"end":9376645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164985.14","gene_symbol":"PSIP1","gene_name":"PC4 and SFRS1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9527]","synonyms":"DFS70,PSIP2,p75,p52,LEDGF","biotype":"protein_coding","ncbi_id":"11168","summary":null,"start":15464066,"end":15511019,"strand":-1,"description":"PC4 and SFRS1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9527]"}, {"versioned_ensembl_gene_id":"ENSG00000110107.8","gene_symbol":"PRPF19","gene_name":"pre-mRNA processing factor 19 [Source:HGNC Symbol;Acc:HGNC:17896]","synonyms":"UBOX4,SNEV,PSO4,PRP19,NMP200,hPSO4","biotype":"protein_coding","ncbi_id":"27339","summary":"PSO4 is the human homolog of yeast Pso4, a gene essential for cell survival and DNA repair (Beck et al., 2008 [PubMed 18263876]).[supplied by OMIM, Sep 2008]","start":60890730,"end":60906588,"strand":-1,"description":"pre-mRNA processing factor 19 [Source:HGNC Symbol;Acc:HGNC:17896]"}, {"versioned_ensembl_gene_id":"ENSG00000279864.1","gene_symbol":"AC124864.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9558970,"end":9559155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166228.8","gene_symbol":"PCBD1","gene_name":"pterin-4 alpha-carbinolamine dehydratase 1 [Source:HGNC Symbol;Acc:HGNC:8646]","synonyms":"PCD,PCBD,DCOH","biotype":"protein_coding","ncbi_id":"5092","summary":"This gene encodes a member of the pterin-4-alpha-carbinolamine dehydratase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The encoded protein functions as both a dehydratase involved in tetrahydrobiopterin biosynthesis, and as a cofactor for HNF1A-dependent transcription. A deficiency of this enzyme leads to hyperphenylalaninemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":70882280,"end":70888784,"strand":-1,"description":"pterin-4 alpha-carbinolamine dehydratase 1 [Source:HGNC Symbol;Acc:HGNC:8646]"}, {"versioned_ensembl_gene_id":"ENSG00000165637.13","gene_symbol":"VDAC2","gene_name":"voltage dependent anion channel 2 [Source:HGNC Symbol;Acc:HGNC:12672]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7417","summary":"This gene encodes a member of the voltage-dependent anion channel pore-forming family of proteins that are considered the main pathway for metabolite diffusion across the mitochondrial outer membrane. The encoded protein is also thought to be involved in the mitochondrial apoptotic pathway via regulation of BCL2-antagonist/killer 1 protein activity. Pseudogenes have been identified on chromosomes 1, 2, 12 and 21, and alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":75210154,"end":75231448,"strand":1,"description":"voltage dependent anion channel 2 [Source:HGNC Symbol;Acc:HGNC:12672]"}, {"versioned_ensembl_gene_id":"ENSG00000156990.14","gene_symbol":"RPUSD3","gene_name":"RNA pseudouridylate synthase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28437]","synonyms":"MGC29784","biotype":"protein_coding","ncbi_id":"285367","summary":"This gene encodes a protein that functions in the assembly of the mitochondrial ribosome by adding a pseudouridine group to 16S rRNA. Loss of this gene results in causes defects in mitochondrial protein production. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2017]","start":9837849,"end":9844602,"strand":-1,"description":"RNA pseudouridylate synthase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28437]"}, {"versioned_ensembl_gene_id":"ENSG00000223433.1","gene_symbol":"RPS29P9","gene_name":"ribosomal protein S29 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648343","summary":null,"start":207654781,"end":207654951,"strand":1,"description":"ribosomal protein S29 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36913]"}, {"versioned_ensembl_gene_id":"ENSG00000224137.1","gene_symbol":"LINC01857","gene_name":"long intergenic non-protein coding RNA 1857 [Source:HGNC Symbol;Acc:HGNC:52673]","synonyms":"AC079767.4","biotype":"lincRNA","ncbi_id":"102724714","summary":null,"start":207662375,"end":207667024,"strand":1,"description":"long intergenic non-protein coding RNA 1857 [Source:HGNC Symbol;Acc:HGNC:52673]"}, {"versioned_ensembl_gene_id":"ENSG00000144712.11","gene_symbol":"CAND2","gene_name":"cullin associated and neddylation dissociated 2 (putative) [Source:HGNC Symbol;Acc:HGNC:30689]","synonyms":"Tp120b,TIP120B,KIAA0667","biotype":"protein_coding","ncbi_id":"23066","summary":null,"start":12796472,"end":12871916,"strand":1,"description":"cullin associated and neddylation dissociated 2 (putative) [Source:HGNC Symbol;Acc:HGNC:30689]"}, {"versioned_ensembl_gene_id":"ENSG00000271409.1","gene_symbol":"AC073176.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70929925,"end":70932057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213082.3","gene_symbol":"PPP1R14BP2","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729406","summary":null,"start":207681590,"end":207682033,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16329]"}, {"versioned_ensembl_gene_id":"ENSG00000090863.11","gene_symbol":"GLG1","gene_name":"golgi glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:4316]","synonyms":"MG-160,ESL-1,CFR-1","biotype":"protein_coding","ncbi_id":"2734","summary":null,"start":74447427,"end":74607144,"strand":-1,"description":"golgi glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:4316]"}, {"versioned_ensembl_gene_id":"ENSG00000226600.3","gene_symbol":"CT47A9","gene_name":"cancer/testis antigen family 47, member A9 [Source:HGNC Symbol;Acc:HGNC:33290]","synonyms":"CT47.9","biotype":"protein_coding","ncbi_id":"728042","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120943561,"end":120946883,"strand":-1,"description":"cancer/testis antigen family 47, member A9 [Source:HGNC Symbol;Acc:HGNC:33290]"}, {"versioned_ensembl_gene_id":"ENSG00000139921.12","gene_symbol":"TMX1","gene_name":"thioredoxin related transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:15487]","synonyms":"TXNDC1,TXNDC,TMX,PDIA11","biotype":"protein_coding","ncbi_id":"81542","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, and one transmembrane domain. Unlike most members of this gene family, it lacks a C-terminal ER-retention sequence. The mature membrane-bound protein can both oxidize and reduce disulfide bonds and acts selectively on membrane-associated polypeptides. [provided by RefSeq, Jan 2017]","start":51240162,"end":51257546,"strand":1,"description":"thioredoxin related transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:15487]"}, {"versioned_ensembl_gene_id":"ENSG00000282514.1","gene_symbol":"AC010724.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":82551263,"end":82552010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157933.9","gene_symbol":"SKI","gene_name":"SKI proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10896]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6497","summary":"This gene encodes the nuclear protooncogene protein homolog of avian sarcoma viral (v-ski) oncogene. It functions as a repressor of TGF-beta signaling, and may play a role in neural tube development and muscle differentiation. [provided by RefSeq, Oct 2009]","start":2228695,"end":2310119,"strand":1,"description":"SKI proto-oncogene [Source:HGNC Symbol;Acc:HGNC:10896]"}, {"versioned_ensembl_gene_id":"ENSG00000203900.2","gene_symbol":"AL121827.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63359988,"end":63371177,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230448.5","gene_symbol":"LINC00276","gene_name":"long intergenic non-protein coding RNA 276 [Source:HGNC Symbol;Acc:HGNC:38663]","synonyms":"NCRNA00276","biotype":"lincRNA","ncbi_id":"100499171","summary":null,"start":13710531,"end":14400963,"strand":-1,"description":"long intergenic non-protein coding RNA 276 [Source:HGNC Symbol;Acc:HGNC:38663]"}, {"versioned_ensembl_gene_id":"ENSG00000234712.1","gene_symbol":"AL713923.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145232929,"end":145233619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213906.9","gene_symbol":"LTB4R2","gene_name":"leukotriene B4 receptor 2 [Source:HGNC Symbol;Acc:HGNC:19260]","synonyms":"NOP9,JULF2,BLTR2,BLT2","biotype":"protein_coding","ncbi_id":"56413","summary":null,"start":24305734,"end":24312053,"strand":1,"description":"leukotriene B4 receptor 2 [Source:HGNC Symbol;Acc:HGNC:19260]"}, {"versioned_ensembl_gene_id":"ENSG00000229370.1","gene_symbol":"AC073062.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13537673,"end":13609168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215054.3","gene_symbol":"HNRNPCP10","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48821]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129229","summary":null,"start":144840777,"end":144841660,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:48821]"}, {"versioned_ensembl_gene_id":"ENSG00000235598.1","gene_symbol":"RRM2P4","gene_name":"ribonucleotide reductase M2 polypeptide pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"6246","summary":null,"start":144309132,"end":144309693,"strand":1,"description":"ribonucleotide reductase M2 polypeptide pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:10456]"}, {"versioned_ensembl_gene_id":"ENSG00000225970.1","gene_symbol":"AL500522.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143757737,"end":143828133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235729.1","gene_symbol":"AL500522.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143806391,"end":143806733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176046.8","gene_symbol":"NUPR1","gene_name":"nuclear protein 1, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29990]","synonyms":"p8,COM1","biotype":"protein_coding","ncbi_id":"26471","summary":null,"start":28532708,"end":28539174,"strand":-1,"description":"nuclear protein 1, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29990]"}, {"versioned_ensembl_gene_id":"ENSG00000273142.1","gene_symbol":"AC073335.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66902857,"end":66906297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130751.9","gene_symbol":"NPAS1","gene_name":"neuronal PAS domain protein 1 [Source:HGNC Symbol;Acc:HGNC:7894]","synonyms":"PASD5,MOP5,bHLHe11","biotype":"protein_coding","ncbi_id":"4861","summary":"The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. Studies of a related mouse gene suggest that it functions in neurons. The exact function of this gene is unclear, but it may play protective or modulatory roles during late embryogenesis and postnatal development. [provided by RefSeq, Jul 2008]","start":47019820,"end":47045775,"strand":1,"description":"neuronal PAS domain protein 1 [Source:HGNC Symbol;Acc:HGNC:7894]"}, {"versioned_ensembl_gene_id":"ENSG00000282627.1","gene_symbol":"IGHV3-48","gene_name":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28424","summary":null,"start":106562491,"end":106563025,"strand":-1,"description":"immunoglobulin heavy variable 3-48 [Source:HGNC Symbol;Acc:HGNC:5606]"}, {"versioned_ensembl_gene_id":"ENSG00000177212.4","gene_symbol":"OR2T33","gene_name":"olfactory receptor family 2 subfamily T member 33 [Source:HGNC Symbol;Acc:HGNC:31255]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391195","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248269917,"end":248277976,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 33 [Source:HGNC Symbol;Acc:HGNC:31255]"}, {"versioned_ensembl_gene_id":"ENSG00000159495.7","gene_symbol":"TGM7","gene_name":"transglutaminase 7 [Source:HGNC Symbol;Acc:HGNC:30790]","synonyms":"TGMZ","biotype":"protein_coding","ncbi_id":"116179","summary":"Transglutaminases (TGM; EC 2.3.2.13) are a family of structurally and functionally related enzymes that stabilize protein assemblies through the formation of gamma-glutamyl-epsilon lysine crosslinks. For additional background information on transglutaminases, see TGM1 (MIM 190195).[supplied by OMIM, Jul 2002]","start":43276280,"end":43302255,"strand":-1,"description":"transglutaminase 7 [Source:HGNC Symbol;Acc:HGNC:30790]"}, {"versioned_ensembl_gene_id":"ENSG00000214727.2","gene_symbol":"RPL5P35","gene_name":"ribosomal protein L5 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36967]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129647","summary":null,"start":49757627,"end":49758980,"strand":-1,"description":"ribosomal protein L5 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36967]"}, {"versioned_ensembl_gene_id":"ENSG00000226954.1","gene_symbol":"AL023802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49718053,"end":49724506,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281986.1","gene_symbol":"IGHV3-36","gene_name":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28431","summary":null,"start":106417455,"end":106417912,"strand":-1,"description":"immunoglobulin heavy variable 3-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5599]"}, {"versioned_ensembl_gene_id":"ENSG00000284741.1","gene_symbol":"PDE11A","gene_name":"phosphodiesterase 11A [Source:NCBI gene;Acc:50940]","synonyms":"PPNAD2","biotype":"protein_coding","ncbi_id":"50940","summary":"The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a member of the PDE protein superfamily. Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":177628069,"end":178108339,"strand":-1,"description":"phosphodiesterase 11A [Source:NCBI gene;Acc:50940]"}, {"versioned_ensembl_gene_id":"ENSG00000131668.13","gene_symbol":"BARX1","gene_name":"BARX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:955]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56033","summary":"This gene encodes a member of the Bar subclass of homeobox transcription factors. Studies of the mouse and chick homolog suggest the encoded protein may play a role in developing teeth and craniofacial mesenchyme of neural crest origin. The protein may also be associated with differentiation of stomach epithelia. [provided by RefSeq, Jul 2008]","start":93951622,"end":93955372,"strand":-1,"description":"BARX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:955]"}, {"versioned_ensembl_gene_id":"ENSG00000213527.5","gene_symbol":"AC026826.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79751689,"end":79752049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165807.7","gene_symbol":"PPP1R36","gene_name":"protein phosphatase 1 regulatory subunit 36 [Source:HGNC Symbol;Acc:HGNC:20097]","synonyms":"C14orf50","biotype":"protein_coding","ncbi_id":"145376","summary":null,"start":64549902,"end":64589380,"strand":1,"description":"protein phosphatase 1 regulatory subunit 36 [Source:HGNC Symbol;Acc:HGNC:20097]"}, {"versioned_ensembl_gene_id":"ENSG00000158485.10","gene_symbol":"CD1B","gene_name":"CD1b molecule [Source:HGNC Symbol;Acc:HGNC:1635]","synonyms":"CD1","biotype":"protein_coding","ncbi_id":"910","summary":"This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail, and requires vesicular acidification to bind lipid antigens. [provided by RefSeq, Jul 2008]","start":158327951,"end":158331531,"strand":-1,"description":"CD1b molecule [Source:HGNC Symbol;Acc:HGNC:1635]"}, {"versioned_ensembl_gene_id":"ENSG00000273838.1","gene_symbol":"AL109954.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23458529,"end":23459459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226344.1","gene_symbol":"CST12P","gene_name":"cystatin 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:31920]","synonyms":"E2,Ctes4,Cst","biotype":"unprocessed_pseudogene","ncbi_id":"106478911","summary":null,"start":23475700,"end":23479798,"strand":1,"description":"cystatin 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:31920]"}, {"versioned_ensembl_gene_id":"ENSG00000279153.1","gene_symbol":"AC117500.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131645918,"end":131646444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120054.11","gene_symbol":"CPN1","gene_name":"carboxypeptidase N subunit 1 [Source:HGNC Symbol;Acc:HGNC:2312]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1369","summary":"Carboxypeptidase N is a plasma metallo-protease that cleaves basic amino acids from the C terminal of peptides and proteins. The enzyme is important in the regulation of peptides like kinins and anaphylatoxins, and has also been known as kininase-1 and anaphylatoxin inactivator. This enzyme is a tetramer comprised of two identical regulatory subunits and two identical catalytic subunits; this gene encodes the catalytic subunit. Mutations in this gene can be associated with angioedema or chronic urticaria resulting from carboxypeptidase N deficiency. [provided by RefSeq, Jul 2008]","start":100042193,"end":100081877,"strand":-1,"description":"carboxypeptidase N subunit 1 [Source:HGNC Symbol;Acc:HGNC:2312]"}, {"versioned_ensembl_gene_id":"ENSG00000272714.1","gene_symbol":"AL139098.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":121389324,"end":121390357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158481.12","gene_symbol":"CD1C","gene_name":"CD1c molecule [Source:HGNC Symbol;Acc:HGNC:1636]","synonyms":"CD1","biotype":"protein_coding","ncbi_id":"911","summary":"This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene is broadly distributed throughout the endocytic system via a tyrosine-based motif in the cytoplasmic tail. Alternatively spliced transcript variants of this gene have been observed, but their full-length nature is not known. [provided by RefSeq, Jul 2008]","start":158289786,"end":158293630,"strand":1,"description":"CD1c molecule [Source:HGNC Symbol;Acc:HGNC:1636]"}, {"versioned_ensembl_gene_id":"ENSG00000233913.7","gene_symbol":"RPL10P9","gene_name":"ribosomal protein L10 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35579]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389342","summary":null,"start":168616352,"end":168616996,"strand":1,"description":"ribosomal protein L10 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35579]"}, {"versioned_ensembl_gene_id":"ENSG00000282480.1","gene_symbol":"AC127071.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130350996,"end":130351707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138735.15","gene_symbol":"PDE5A","gene_name":"phosphodiesterase 5A [Source:HGNC Symbol;Acc:HGNC:8784]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8654","summary":"This gene encodes a cGMP-binding, cGMP-specific phosphodiesterase, a member of the cyclic nucleotide phosphodiesterase family. This phosphodiesterase specifically hydrolyzes cGMP to 5'-GMP. It is involved in the regulation of intracellular concentrations of cyclic nucleotides and is important for smooth muscle relaxation in the cardiovascular system. Alternative splicing of this gene results in three transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":119494395,"end":119628991,"strand":-1,"description":"phosphodiesterase 5A [Source:HGNC Symbol;Acc:HGNC:8784]"}, {"versioned_ensembl_gene_id":"ENSG00000111801.15","gene_symbol":"BTN3A3","gene_name":"butyrophilin subfamily 3 member A3 [Source:HGNC Symbol;Acc:HGNC:1140]","synonyms":"BTF3,BTN3.3","biotype":"protein_coding","ncbi_id":"10384","summary":"The butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC)-associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30.2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single-copy BTN1A1 gene (MIM 601610) and the BTN2 (e.g., BTN2A1; MIM 613590) and BTN3 (e.g., BNT3A3) genes, which have undergone tandem duplication, resulting in 3 copies of each (summary by Smith et al., 2010 [PubMed 20208008]).[supplied by OMIM, Nov 2010]","start":26440472,"end":26453415,"strand":1,"description":"butyrophilin subfamily 3 member A3 [Source:HGNC Symbol;Acc:HGNC:1140]"}, {"versioned_ensembl_gene_id":"ENSG00000175634.14","gene_symbol":"RPS6KB2","gene_name":"ribosomal protein S6 kinase B2 [Source:HGNC Symbol;Acc:HGNC:10437]","synonyms":"STK14B,p70S6Kb,P70-BETA,KLS","biotype":"protein_coding","ncbi_id":"6199","summary":"This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains a kinase catalytic domain and phosphorylates the S6 ribosomal protein and eukaryotic translation initiation factor 4B (eIF4B). Phosphorylation of S6 leads to an increase in protein synthesis and cell proliferation. [provided by RefSeq, Jan 2015]","start":67428460,"end":67435408,"strand":1,"description":"ribosomal protein S6 kinase B2 [Source:HGNC Symbol;Acc:HGNC:10437]"}, {"versioned_ensembl_gene_id":"ENSG00000230569.1","gene_symbol":"AC114763.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138470656,"end":138473932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275136.4","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54874257,"end":54890481,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000125388.19","gene_symbol":"GRK4","gene_name":"G protein-coupled receptor kinase 4 [Source:HGNC Symbol;Acc:HGNC:4543]","synonyms":"GPRK4,GPRK2L","biotype":"protein_coding","ncbi_id":"2868","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating its deactivation. This gene has been linked to both genetic and acquired hypertension. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":2963608,"end":3040747,"strand":1,"description":"G protein-coupled receptor kinase 4 [Source:HGNC Symbol;Acc:HGNC:4543]"}, {"versioned_ensembl_gene_id":"ENSG00000229753.1","gene_symbol":"RPS27AP15","gene_name":"ribosomal protein S27a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35817]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271379","summary":null,"start":72741152,"end":72741617,"strand":-1,"description":"ribosomal protein S27a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35817]"}, {"versioned_ensembl_gene_id":"ENSG00000234713.3","gene_symbol":"AC022616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43276270,"end":43276823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230400.2","gene_symbol":"LINC01747","gene_name":"long intergenic non-protein coding RNA 1747 [Source:HGNC Symbol;Acc:HGNC:52536]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372566","summary":null,"start":22668484,"end":22685344,"strand":-1,"description":"long intergenic non-protein coding RNA 1747 [Source:HGNC Symbol;Acc:HGNC:52536]"}, {"versioned_ensembl_gene_id":"ENSG00000125831.9","gene_symbol":"CST11","gene_name":"cystatin 11 [Source:HGNC Symbol;Acc:HGNC:15959]","synonyms":"CST8L,dJ322G13.6,CTES2","biotype":"protein_coding","ncbi_id":"140880","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes an epididymal-specific protein shown to have antimicrobial activity against E. coli. Alternative splicing yields two variants encoding distinct isoforms. [provided by RefSeq, Sep 2014]","start":23450403,"end":23452857,"strand":-1,"description":"cystatin 11 [Source:HGNC Symbol;Acc:HGNC:15959]"}, {"versioned_ensembl_gene_id":"ENSG00000281959.1","gene_symbol":"AC234301.2","gene_name":null,"synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":null,"summary":null,"start":106369091,"end":106369528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158477.6","gene_symbol":"CD1A","gene_name":"CD1a molecule [Source:HGNC Symbol;Acc:HGNC:1634]","synonyms":"CD1","biotype":"protein_coding","ncbi_id":"909","summary":"This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to the plasma membrane and to recycling vesicles of the early endocytic system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":158254137,"end":158258269,"strand":1,"description":"CD1a molecule [Source:HGNC Symbol;Acc:HGNC:1634]"}, {"versioned_ensembl_gene_id":"ENSG00000282136.1","gene_symbol":"IGHVII-30-1","gene_name":"immunoglobulin heavy variable (II)-30-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5676]","synonyms":"IGHV(II)-30-1","biotype":"IG_V_pseudogene","ncbi_id":"28371","summary":null,"start":106343495,"end":106343726,"strand":-1,"description":"immunoglobulin heavy variable (II)-30-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5676]"}, {"versioned_ensembl_gene_id":"ENSG00000254118.1","gene_symbol":"MTCYBP20","gene_name":"mitochondrially encoded cytochrome b pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075128","summary":null,"start":46837578,"end":46838706,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51973]"}, {"versioned_ensembl_gene_id":"ENSG00000235008.1","gene_symbol":"AL023775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166701094,"end":166702839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228563.1","gene_symbol":"AL133247.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31526942,"end":31563464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121297.6","gene_symbol":"TSHZ3","gene_name":"teashirt zinc finger homeobox 3 [Source:HGNC Symbol;Acc:HGNC:30700]","synonyms":"ZNF537,TSH3,KIAA1474","biotype":"protein_coding","ncbi_id":"57616","summary":"This gene encodes a zinc-finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits caspase expression. Reduced expression of this gene and consequent caspase upregulation may be correlated with progression of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2016]","start":31274945,"end":31349547,"strand":-1,"description":"teashirt zinc finger homeobox 3 [Source:HGNC Symbol;Acc:HGNC:30700]"}, {"versioned_ensembl_gene_id":"ENSG00000241257.1","gene_symbol":"AC124945.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109364047,"end":109364234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278006.2","gene_symbol":"CCL18","gene_name":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]","synonyms":"CKb7,SCYA18,AMAC-1,PARC,MIP-4,DCCK1,DC-CK1","biotype":"protein_coding","ncbi_id":"6362","summary":"This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for naive T cells, CD4+ and CD8+ T cells and nonactivated lymphocytes, but not for monocytes or granulocytes. This chemokine attracts naive T lymphocytes toward dendritic cells and activated macrophages in lymph nodes. It may play a role in both humoral and cell-mediated immunity responses. [provided by RefSeq, Sep 2014]","start":36064280,"end":36072032,"strand":1,"description":"C-C motif chemokine ligand 18 [Source:HGNC Symbol;Acc:HGNC:10616]"}, {"versioned_ensembl_gene_id":"ENSG00000125675.17","gene_symbol":"GRIA3","gene_name":"glutamate ionotropic receptor AMPA type subunit 3 [Source:HGNC Symbol;Acc:HGNC:4573]","synonyms":"MRX94,GLURC,GLUR3,GluA3","biotype":"protein_coding","ncbi_id":"2892","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes composed of multiple subunits, arranged to form ligand-gated ion channels. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. The subunit encoded by this gene belongs to a family of AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate)-sensitive glutamate receptors, and is subject to RNA editing (AGA->GGA; R->G). Alternative splicing at this locus results in different isoforms, which may vary in their signal transduction properties. [provided by RefSeq, Jul 2008]","start":123184153,"end":123490915,"strand":1,"description":"glutamate ionotropic receptor AMPA type subunit 3 [Source:HGNC Symbol;Acc:HGNC:4573]"}, {"versioned_ensembl_gene_id":"ENSG00000273592.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173824,"end":54190479,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000127946.16","gene_symbol":"HIP1","gene_name":"huntingtin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:4913]","synonyms":"ILWEQ","biotype":"protein_coding","ncbi_id":"3092","summary":"The product of this gene is a membrane-associated protein that functions in clathrin-mediated endocytosis and protein trafficking within the cell. The encoded protein binds to the huntingtin protein in the brain; this interaction is lost in Huntington's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":75533300,"end":75738962,"strand":-1,"description":"huntingtin interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:4913]"}, {"versioned_ensembl_gene_id":"ENSG00000171700.13","gene_symbol":"RGS19","gene_name":"regulator of G protein signaling 19 [Source:HGNC Symbol;Acc:HGNC:13735]","synonyms":"RGSGAIP,GAIP","biotype":"protein_coding","ncbi_id":"10287","summary":"G proteins mediate a number of cellular processes. The protein encoded by this gene belongs to the RGS (regulators of G-protein signaling) family and specifically interacts with G protein, GAI3. This protein is a guanosine triphosphatase-activating protein that functions to down-regulate Galpha i/Galpha q-linked signaling. Alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":64073181,"end":64079988,"strand":-1,"description":"regulator of G protein signaling 19 [Source:HGNC Symbol;Acc:HGNC:13735]"}, {"versioned_ensembl_gene_id":"ENSG00000281326.1","gene_symbol":"AC009286.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22474747,"end":22475074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223859.1","gene_symbol":"AC007403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67040546,"end":67041966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104643.9","gene_symbol":"MTMR9","gene_name":"myotubularin related protein 9 [Source:HGNC Symbol;Acc:HGNC:14596]","synonyms":"MTMR8,LIP-STYX,DKFZp434K171,C8orf9","biotype":"protein_coding","ncbi_id":"66036","summary":"This gene encodes a myotubularin-related protein that is atypical to most other members of the myotubularin-related protein family because it has no dual-specificity phosphatase domain. The encoded protein contains a double-helical motif similar to the SET interaction domain, which is thought to have a role in the control of cell proliferation. In mouse, a protein similar to the encoded protein binds with MTMR7, and together they dephosphorylate phosphatidylinositol 3-phosphate and inositol 1,3-bisphosphate. [provided by RefSeq, Jul 2008]","start":11284416,"end":11328146,"strand":1,"description":"myotubularin related protein 9 [Source:HGNC Symbol;Acc:HGNC:14596]"}, {"versioned_ensembl_gene_id":"ENSG00000265487.1","gene_symbol":"AP001021.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5956101,"end":5960785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225711.1","gene_symbol":"AL512326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179220938,"end":179222125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227183.3","gene_symbol":"HDGFP1","gene_name":"heparin binding growth factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31836]","synonyms":"HDGFP","biotype":"processed_pseudogene","ncbi_id":"474167","summary":null,"start":131646639,"end":131646890,"strand":1,"description":"heparin binding growth factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31836]"}, {"versioned_ensembl_gene_id":"ENSG00000253425.2","gene_symbol":"HSPA8P13","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44928]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480803","summary":null,"start":46549089,"end":46550802,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:44928]"}, {"versioned_ensembl_gene_id":"ENSG00000078142.12","gene_symbol":"PIK3C3","gene_name":"phosphatidylinositol 3-kinase catalytic subunit type 3 [Source:HGNC Symbol;Acc:HGNC:8974]","synonyms":"Vps34","biotype":"protein_coding","ncbi_id":"5289","summary":null,"start":41955206,"end":42087830,"strand":1,"description":"phosphatidylinositol 3-kinase catalytic subunit type 3 [Source:HGNC Symbol;Acc:HGNC:8974]"}, {"versioned_ensembl_gene_id":"ENSG00000213247.3","gene_symbol":"AL355863.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111104956,"end":111105248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232620.1","gene_symbol":"TSPY17P","gene_name":"testis specific protein, Y-linked 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:37713]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132124","summary":null,"start":6520463,"end":6520929,"strand":1,"description":"testis specific protein, Y-linked 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:37713]"}, {"versioned_ensembl_gene_id":"ENSG00000265060.1","gene_symbol":"PPY2P","gene_name":"pancreatic polypeptide 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:9328]","synonyms":"PPY2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"23614","summary":null,"start":28247444,"end":28248289,"strand":1,"description":"pancreatic polypeptide 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:9328]"}, {"versioned_ensembl_gene_id":"ENSG00000096433.10","gene_symbol":"ITPR3","gene_name":"inositol 1,4,5-trisphosphate receptor type 3 [Source:HGNC Symbol;Acc:HGNC:6182]","synonyms":"IP3R3","biotype":"protein_coding","ncbi_id":"3710","summary":"This gene encodes a receptor for inositol 1,4,5-trisphosphate, a second messenger that mediates the release of intracellular calcium. The receptor contains a calcium channel at the C-terminus and the ligand-binding site at the N-terminus. Knockout studies in mice suggest that type 2 and type 3 inositol 1,4,5-trisphosphate receptors play a key role in exocrine secretion underlying energy metabolism and growth. [provided by RefSeq, Aug 2010]","start":33620365,"end":33696574,"strand":1,"description":"inositol 1,4,5-trisphosphate receptor type 3 [Source:HGNC Symbol;Acc:HGNC:6182]"}, {"versioned_ensembl_gene_id":"ENSG00000137288.9","gene_symbol":"UQCC2","gene_name":"ubiquinol-cytochrome c reductase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:21237]","synonyms":"bA6B20.2,MNF1,MGC14833,M19,Cbp6,C6orf125","biotype":"protein_coding","ncbi_id":"84300","summary":"This gene encodes a nucleoid protein localized to the mitochondria inner membrane. The encoded protein affects regulation of insulin secretion, mitochondrial ATP production, and myogenesis through modulation of mitochondrial respiratory chain activity. [provided by RefSeq, Oct 2012]","start":33694293,"end":33711727,"strand":-1,"description":"ubiquinol-cytochrome c reductase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:21237]"}, {"versioned_ensembl_gene_id":"ENSG00000277276.3","gene_symbol":"OTUB2","gene_name":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]","synonyms":"FLJ21916,C14orf137,MGC3102","biotype":"protein_coding","ncbi_id":"78990","summary":"This gene encodes one of several deubiquitylating enzymes. Ubiquitin modification of proteins is needed for their stability and function; to reverse the process, deubiquityling enzymes remove ubiquitin. This protein contains an OTU domain and binds Ubal (ubiquitin aldehyde); an active cysteine protease site is present in the OTU domain. [provided by RefSeq, Aug 2011]","start":94026329,"end":94049624,"strand":1,"description":"OTU deubiquitinase, ubiquitin aldehyde binding 2 [Source:HGNC Symbol;Acc:HGNC:20351]"}, {"versioned_ensembl_gene_id":"ENSG00000277240.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000182240.15","gene_symbol":"BACE2","gene_name":"beta-site APP-cleaving enzyme 2 [Source:HGNC Symbol;Acc:HGNC:934]","synonyms":"CEAP1,ALP56,AEPLC,DRAP","biotype":"protein_coding","ncbi_id":"25825","summary":"This gene encodes an integral membrane glycoprotein that functions as an aspartic protease. The encoded protein cleaves amyloid precursor protein into amyloid beta peptide, which is a critical step in the etiology of Alzheimer's disease and Down syndrome. The protein precursor is further processed into an active mature peptide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":41167801,"end":41282518,"strand":1,"description":"beta-site APP-cleaving enzyme 2 [Source:HGNC Symbol;Acc:HGNC:934]"}, {"versioned_ensembl_gene_id":"ENSG00000225473.1","gene_symbol":"ATP13A4-AS1","gene_name":"ATP13A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41095]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929198","summary":null,"start":193553213,"end":193555088,"strand":1,"description":"ATP13A4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41095]"}, {"versioned_ensembl_gene_id":"ENSG00000226496.2","gene_symbol":"LINC00323","gene_name":"long intergenic non-protein coding RNA 323 [Source:HGNC Symbol;Acc:HGNC:19720]","synonyms":"PRED42,NCRNA00323,FLJ37173,C21orf130","biotype":"antisense_RNA","ncbi_id":"284835","summary":null,"start":41141493,"end":41148133,"strand":-1,"description":"long intergenic non-protein coding RNA 323 [Source:HGNC Symbol;Acc:HGNC:19720]"}, {"versioned_ensembl_gene_id":"ENSG00000256339.1","gene_symbol":"AC007655.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14841092,"end":14844708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282205.1","gene_symbol":"AC115090.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":38251172,"end":38253222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171766.15","gene_symbol":"GATM","gene_name":"glycine amidinotransferase [Source:HGNC Symbol;Acc:HGNC:4175]","synonyms":"AGAT","biotype":"protein_coding","ncbi_id":"2628","summary":"This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by cognitive disability, language impairment, and behavioral disorders. [provided by RefSeq, Jul 2008]","start":45361124,"end":45402327,"strand":-1,"description":"glycine amidinotransferase [Source:HGNC Symbol;Acc:HGNC:4175]"}, {"versioned_ensembl_gene_id":"ENSG00000255365.1","gene_symbol":"AC040926.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14690382,"end":14690619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275672.1","gene_symbol":"AC025580.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45378700,"end":45380123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231565.1","gene_symbol":"NEK2P2","gene_name":"NEK2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37816]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100379667","summary":null,"start":15611759,"end":15613096,"strand":-1,"description":"NEK2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37816]"}, {"versioned_ensembl_gene_id":"ENSG00000243806.1","gene_symbol":"RPL7P18","gene_name":"ribosomal protein L7 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36949]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270852","summary":null,"start":94825961,"end":94826694,"strand":-1,"description":"ribosomal protein L7 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36949]"}, {"versioned_ensembl_gene_id":"ENSG00000177144.7","gene_symbol":"NUDT4P1","gene_name":"nudix hydrolase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18012]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440672","summary":null,"start":148748894,"end":148750099,"strand":1,"description":"nudix hydrolase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18012]"}, {"versioned_ensembl_gene_id":"ENSG00000145332.13","gene_symbol":"KLHL8","gene_name":"kelch like family member 8 [Source:HGNC Symbol;Acc:HGNC:18644]","synonyms":"KIAA1378","biotype":"protein_coding","ncbi_id":"57563","summary":null,"start":87160103,"end":87240314,"strand":-1,"description":"kelch like family member 8 [Source:HGNC Symbol;Acc:HGNC:18644]"}, {"versioned_ensembl_gene_id":"ENSG00000109920.12","gene_symbol":"FNBP4","gene_name":"formin binding protein 4 [Source:HGNC Symbol;Acc:HGNC:19752]","synonyms":"KIAA1014","biotype":"protein_coding","ncbi_id":"23360","summary":"This gene encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome. [provided by RefSeq, Apr 2017]","start":47716517,"end":47767443,"strand":-1,"description":"formin binding protein 4 [Source:HGNC Symbol;Acc:HGNC:19752]"}, {"versioned_ensembl_gene_id":"ENSG00000162711.16","gene_symbol":"NLRP3","gene_name":"NLR family pyrin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:16400]","synonyms":"CLR1.1,CIAS1,C1orf7,AVP,PYPAF1,AII,NALP3,AGTAVPRL,MWS,FCU,FCAS","biotype":"protein_coding","ncbi_id":"114548","summary":"This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NLRP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. The SARS-CoV 3a protein, a transmembrane pore-forming viroporin, has been shown to activate the NLRP3 inflammasome via the formation of ion channels in macrophages. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, neonatal-onset multisystem inflammatory disease (NOMID), keratoendotheliitis fugax hereditarian, and deafness, autosomal dominant 34, with or without inflammation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Aug 2020]","start":247416156,"end":247449108,"strand":1,"description":"NLR family pyrin domain containing 3 [Source:HGNC Symbol;Acc:HGNC:16400]"}, {"versioned_ensembl_gene_id":"ENSG00000125812.15","gene_symbol":"GZF1","gene_name":"GDNF inducible zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:15808]","synonyms":"ZNF336,ZBTB23,dJ322G13.2","biotype":"protein_coding","ncbi_id":"64412","summary":null,"start":23362182,"end":23373063,"strand":1,"description":"GDNF inducible zinc finger protein 1 [Source:HGNC Symbol;Acc:HGNC:15808]"}, {"versioned_ensembl_gene_id":"ENSG00000263014.5","gene_symbol":"ATP6V1G3","gene_name":"ATPase H+ transporting V1 subunit G3 [Source:HGNC Symbol;Acc:HGNC:18265]","synonyms":"Vma10,ATP6G3","biotype":"protein_coding","ncbi_id":"127124","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'' and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes one of three G subunit proteins. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":198534710,"end":198552432,"strand":-1,"description":"ATPase H+ transporting V1 subunit G3 [Source:HGNC Symbol;Acc:HGNC:18265]"}, {"versioned_ensembl_gene_id":"ENSG00000253452.5","gene_symbol":"AC100818.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35862123,"end":35970665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233454.1","gene_symbol":"AC069285.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63057453,"end":63060084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253501.1","gene_symbol":"IGKV3D-34","gene_name":"immunoglobulin kappa variable 3D-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5828]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28871","summary":null,"start":89906757,"end":89907246,"strand":1,"description":"immunoglobulin kappa variable 3D-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5828]"}, {"versioned_ensembl_gene_id":"ENSG00000134250.19","gene_symbol":"NOTCH2","gene_name":"notch 2 [Source:HGNC Symbol;Acc:HGNC:7882]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4853","summary":"This gene encodes a member of the Notch family. Members of this Type 1 transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple, different domain types. Notch family members play a role in a variety of developmental processes by controlling cell fate decisions. The Notch signaling network is an evolutionarily conserved intercellular signaling pathway which regulates interactions between physically adjacent cells. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signaling pathway that plays a key role in development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remain to be determined. This protein is cleaved in the trans-Golgi network, and presented on the cell surface as a heterodimer. This protein functions as a receptor for membrane bound ligands, and may play a role in vascular, renal and hepatic development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":119911553,"end":120069626,"strand":-1,"description":"notch 2 [Source:HGNC Symbol;Acc:HGNC:7882]"}, {"versioned_ensembl_gene_id":"ENSG00000261364.1","gene_symbol":"AC063923.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109176438,"end":109177365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181001.2","gene_symbol":"OR52N1","gene_name":"olfactory receptor family 52 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:14853]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5786471,"end":5791265,"strand":-1,"description":"olfactory receptor family 52 subfamily N member 1 [Source:HGNC Symbol;Acc:HGNC:14853]"}, {"versioned_ensembl_gene_id":"ENSG00000230403.1","gene_symbol":"LINC01066","gene_name":"long intergenic non-protein coding RNA 1066 [Source:HGNC Symbol;Acc:HGNC:49104]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144544","summary":null,"start":30995162,"end":30996138,"strand":-1,"description":"long intergenic non-protein coding RNA 1066 [Source:HGNC Symbol;Acc:HGNC:49104]"}, {"versioned_ensembl_gene_id":"ENSG00000181009.5","gene_symbol":"OR52N5","gene_name":"olfactory receptor family 52 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15231]","synonyms":"OR52N5Q","biotype":"protein_coding","ncbi_id":"390075","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5776165,"end":5783355,"strand":-1,"description":"olfactory receptor family 52 subfamily N member 5 [Source:HGNC Symbol;Acc:HGNC:15231]"}, {"versioned_ensembl_gene_id":"ENSG00000129315.10","gene_symbol":"CCNT1","gene_name":"cyclin T1 [Source:HGNC Symbol;Acc:HGNC:1599]","synonyms":"HIVE1,CYCT1,CCNT","biotype":"protein_coding","ncbi_id":"904","summary":"This gene encodes a member of the highly conserved cyclin C subfamily. The encoded protein tightly associates with cyclin-dependent kinase 9, and is a major subunit of positive transcription elongation factor b (p-TEFb). In humans, there are multiple forms of positive transcription elongation factor b, which may include one of several different cyclins along with cyclin-dependent kinase 9. The complex containing the encoded cyclin and cyclin-dependent kinase 9 acts as a cofactor of human immunodeficiency virus type 1 (HIV-1) Tat protein, and is both necessary and sufficient for full activation of viral transcription. This cyclin and its kinase partner are also involved in triggering transcript elongation through phosphorylation of the carboxy-terminal domain of the largest RNA polymerase II subunit. Overexpression of this gene is implicated in tumor growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]","start":48688458,"end":48716998,"strand":-1,"description":"cyclin T1 [Source:HGNC Symbol;Acc:HGNC:1599]"}, {"versioned_ensembl_gene_id":"ENSG00000183269.5","gene_symbol":"OR52E8","gene_name":"olfactory receptor family 52 subfamily E member 8 [Source:HGNC Symbol;Acc:HGNC:15217]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390079","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5856674,"end":5857734,"strand":-1,"description":"olfactory receptor family 52 subfamily E member 8 [Source:HGNC Symbol;Acc:HGNC:15217]"}, {"versioned_ensembl_gene_id":"ENSG00000282574.1","gene_symbol":"AC243824.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16308165,"end":16309399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270110.1","gene_symbol":"AL353593.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228295911,"end":228302998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079974.17","gene_symbol":"RABL2B","gene_name":"RAB, member of RAS oncogene family like 2B [Source:HGNC Symbol;Acc:HGNC:9800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11158","summary":"The RABL2B protein is a member of the RAB gene family which belongs to the RAS GTPase superfamily. RABL2B is located within a subtelomeric region of 22q13.3. Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":50767501,"end":50783663,"strand":-1,"description":"RAB, member of RAS oncogene family like 2B [Source:HGNC Symbol;Acc:HGNC:9800]"}, {"versioned_ensembl_gene_id":"ENSG00000213780.10","gene_symbol":"GTF2H4","gene_name":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]","synonyms":"TFB2,P52,TFIIH","biotype":"protein_coding","ncbi_id":"2968","summary":null,"start":30908184,"end":30914106,"strand":1,"description":"general transcription factor IIH subunit 4 [Source:HGNC Symbol;Acc:HGNC:4658]"}, {"versioned_ensembl_gene_id":"ENSG00000165509.13","gene_symbol":"MAGEC3","gene_name":"MAGE family member C3 [Source:HGNC Symbol;Acc:HGNC:23798]","synonyms":"HCA2,CT7.2,MAGE-C3","biotype":"protein_coding","ncbi_id":"139081","summary":"This gene is a member of the MAGEC gene family. The members of this family are not expressed in normal tissues, except for testis, and are expressed in tumors of various histological types. The MAGEC genes are clustered on chromosome Xq26-q27. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":141838316,"end":141897832,"strand":1,"description":"MAGE family member C3 [Source:HGNC Symbol;Acc:HGNC:23798]"}, {"versioned_ensembl_gene_id":"ENSG00000232738.1","gene_symbol":"AL353612.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9575608,"end":9577689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136026.13","gene_symbol":"CKAP4","gene_name":"cytoskeleton associated protein 4 [Source:HGNC Symbol;Acc:HGNC:16991]","synonyms":"P63,ERGIC-63,CLIMP-63","biotype":"protein_coding","ncbi_id":"10970","summary":null,"start":106237877,"end":106304279,"strand":-1,"description":"cytoskeleton associated protein 4 [Source:HGNC Symbol;Acc:HGNC:16991]"}, {"versioned_ensembl_gene_id":"ENSG00000260280.5","gene_symbol":"SLX1B-SULT1A4","gene_name":"SLX1B-SULT1A4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48353]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100526831","summary":"This locus represents naturally occurring read-through transcription between the neighboring SLX1B (SLX1 structure-specific endonuclease subunit homolog B) and SULT1A4 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 4) genes on the short arm of chromosome 16. A duplicate read-through locus also exists between the SLX1A and SULT1A3 genes located approximately 730 kb downstream on the same chromosome. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2017]","start":29455105,"end":29464963,"strand":1,"description":"SLX1B-SULT1A4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48353]"}, {"versioned_ensembl_gene_id":"ENSG00000245614.3","gene_symbol":"DDX11-AS1","gene_name":"DDX11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44176]","synonyms":"CONCR","biotype":"antisense_RNA","ncbi_id":"100506660","summary":null,"start":31020763,"end":31073847,"strand":-1,"description":"DDX11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44176]"}, {"versioned_ensembl_gene_id":"ENSG00000259389.2","gene_symbol":"H3F3AP1","gene_name":"H3 histone family member 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31028]","synonyms":"HsT18159","biotype":"processed_pseudogene","ncbi_id":"654505","summary":null,"start":39951375,"end":39951708,"strand":-1,"description":"H3 histone family member 3A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31028]"}, {"versioned_ensembl_gene_id":"ENSG00000267081.1","gene_symbol":"AC011507.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30850975,"end":30872507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233278.1","gene_symbol":"RPS26P2","gene_name":"ribosomal protein S26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23662]","synonyms":"bA98O11.1","biotype":"processed_pseudogene","ncbi_id":"646753","summary":null,"start":30831878,"end":30832225,"strand":-1,"description":"ribosomal protein S26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23662]"}, {"versioned_ensembl_gene_id":"ENSG00000258162.2","gene_symbol":"AC069228.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81378042,"end":81472954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118257.16","gene_symbol":"NRP2","gene_name":"neuropilin 2 [Source:HGNC Symbol;Acc:HGNC:8005]","synonyms":"VEGF165R2","biotype":"protein_coding","ncbi_id":"8828","summary":"This gene encodes a member of the neuropilin family of receptor proteins. The encoded transmembrane protein binds to SEMA3C protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C} and SEMA3F protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F}, and interacts with vascular endothelial growth factor (VEGF). This protein may play a role in cardiovascular development, axon guidance, and tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":205681990,"end":205798133,"strand":1,"description":"neuropilin 2 [Source:HGNC Symbol;Acc:HGNC:8005]"}, {"versioned_ensembl_gene_id":"ENSG00000164542.12","gene_symbol":"KIAA0895","gene_name":"KIAA0895 [Source:HGNC Symbol;Acc:HGNC:22206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23366","summary":null,"start":36324221,"end":36390125,"strand":-1,"description":"KIAA0895 [Source:HGNC Symbol;Acc:HGNC:22206]"}, {"versioned_ensembl_gene_id":"ENSG00000256045.2","gene_symbol":"MTRNR2L10","gene_name":"MT-RNR2-like 10 [Source:HGNC Symbol;Acc:HGNC:37167]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463488","summary":null,"start":55181391,"end":55182920,"strand":-1,"description":"MT-RNR2-like 10 [Source:HGNC Symbol;Acc:HGNC:37167]"}, {"versioned_ensembl_gene_id":"ENSG00000282329.1","gene_symbol":"MREGP1","gene_name":"melanoregulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480304","summary":null,"start":31256634,"end":31256718,"strand":-1,"description":"melanoregulin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50749]"}, {"versioned_ensembl_gene_id":"ENSG00000224653.1","gene_symbol":"AC023141.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57819819,"end":57820627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271433.1","gene_symbol":"PPATP2","gene_name":"phosphoribosyl pyrophosphate amidotransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48738]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421601","summary":null,"start":78699384,"end":78699891,"strand":-1,"description":"phosphoribosyl pyrophosphate amidotransferase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48738]"}, {"versioned_ensembl_gene_id":"ENSG00000238047.1","gene_symbol":"MTND1P30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42079]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507157","summary":null,"start":55180377,"end":55181277,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42079]"}, {"versioned_ensembl_gene_id":"ENSG00000106258.13","gene_symbol":"CYP3A5","gene_name":"cytochrome P450 family 3 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:2638]","synonyms":"PCN3,P450PCN3,CP35","biotype":"protein_coding","ncbi_id":"1577","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein metabolizes drugs as well as the steroid hormones testosterone and progesterone. This gene is part of a cluster of cytochrome P450 genes on chromosome 7q21.1. Two pseudogenes of this gene have been identified within this cluster on chromosome 7. Expression of this gene is widely variable among populations, and a single nucleotide polymorphism that affects transcript splicing has been associated with susceptibility to hypertensions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":99648194,"end":99679998,"strand":-1,"description":"cytochrome P450 family 3 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:2638]"}, {"versioned_ensembl_gene_id":"ENSG00000260412.1","gene_symbol":"AL353746.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":27937617,"end":27944497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273794.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769825,"end":54784337,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000175676.15","gene_symbol":"GOLGA8EP","gene_name":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]","synonyms":"GOLGA8E","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390535","summary":null,"start":23157366,"end":23170711,"strand":1,"description":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]"}, {"versioned_ensembl_gene_id":"ENSG00000168477.17","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"XB,TNXB2,TNXBS,XBS,TNXB1","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32041154,"end":32115334,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000241878.11","gene_symbol":"PISD","gene_name":"phosphatidylserine decarboxylase [Source:HGNC Symbol;Acc:HGNC:8999]","synonyms":"PSDC,dJ858B16.2","biotype":"protein_coding","ncbi_id":"23761","summary":"The protein encoded by this gene catalyzes the conversion of phosphatidylserine to phosphatidylethanolamine in the inner mitochondrial membrane. The encoded protein is active in phospholipid metabolism and interorganelle trafficking of phosphatidylserine. [provided by RefSeq, May 2016]","start":31618491,"end":31662432,"strand":-1,"description":"phosphatidylserine decarboxylase [Source:HGNC Symbol;Acc:HGNC:8999]"}, {"versioned_ensembl_gene_id":"ENSG00000113595.14","gene_symbol":"TRIM23","gene_name":"tripartite motif containing 23 [Source:HGNC Symbol;Acc:HGNC:660]","synonyms":"RNF46,ARFD1,ARD1","biotype":"protein_coding","ncbi_id":"373","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein is also a member of the ADP ribosylation factor family of guanine nucleotide-binding family of proteins. Its carboxy terminus contains an ADP-ribosylation factor domain and a guanine nucleotide binding site, while the amino terminus contains a GTPase activating protein domain which acts on the guanine nucleotide binding site. The protein localizes to lysosomes and the Golgi apparatus. It plays a role in the formation of intracellular transport vesicles, their movement from one compartment to another, and phopholipase D activation. Three alternatively spliced transcript variants for this gene have been described. [provided by RefSeq, Jul 2008]","start":65589680,"end":65625975,"strand":-1,"description":"tripartite motif containing 23 [Source:HGNC Symbol;Acc:HGNC:660]"}, {"versioned_ensembl_gene_id":"ENSG00000100147.13","gene_symbol":"CCDC134","gene_name":"coiled-coil domain containing 134 [Source:HGNC Symbol;Acc:HGNC:26185]","synonyms":"FLJ22349","biotype":"protein_coding","ncbi_id":"79879","summary":null,"start":41800679,"end":41826299,"strand":1,"description":"coiled-coil domain containing 134 [Source:HGNC Symbol;Acc:HGNC:26185]"}, {"versioned_ensembl_gene_id":"ENSG00000117174.10","gene_symbol":"ZNHIT6","gene_name":"zinc finger HIT-type containing 6 [Source:HGNC Symbol;Acc:HGNC:26089]","synonyms":"NY-BR-75,FLJ20729,C1orf181,BCD1","biotype":"protein_coding","ncbi_id":"54680","summary":null,"start":85649423,"end":85708433,"strand":-1,"description":"zinc finger HIT-type containing 6 [Source:HGNC Symbol;Acc:HGNC:26089]"}, {"versioned_ensembl_gene_id":"ENSG00000235930.3","gene_symbol":"HSPE1P12","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49331]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100286954","summary":null,"start":10770305,"end":10770605,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49331]"}, {"versioned_ensembl_gene_id":"ENSG00000227015.1","gene_symbol":"AC023141.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57770619,"end":57770946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160213.6","gene_symbol":"CSTB","gene_name":"cystatin B [Source:HGNC Symbol;Acc:HGNC:2482]","synonyms":"STFB,PME,EPM1,CST6","biotype":"protein_coding","ncbi_id":"1476","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and kininogens. This gene encodes a stefin that functions as an intracellular thiol protease inhibitor. The protein is able to form a dimer stabilized by noncovalent forces, inhibiting papain and cathepsins l, h and b. The protein is thought to play a role in protecting against the proteases leaking from lysosomes. Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1). One type of mutation responsible for EPM1 is the expansion in the promoter region of this gene of a CCCCGCCCCGCG repeat from 2-3 copies to 30-78 copies. [provided by RefSeq, Jul 2016]","start":43772511,"end":43776445,"strand":-1,"description":"cystatin B [Source:HGNC Symbol;Acc:HGNC:2482]"}, {"versioned_ensembl_gene_id":"ENSG00000173421.16","gene_symbol":"CCDC36","gene_name":"coiled-coil domain containing 36 [Source:HGNC Symbol;Acc:HGNC:27945]","synonyms":"FLJ25320,CT74","biotype":"protein_coding","ncbi_id":"339834","summary":null,"start":49198428,"end":49258104,"strand":1,"description":"coiled-coil domain containing 36 [Source:HGNC Symbol;Acc:HGNC:27945]"}, {"versioned_ensembl_gene_id":"ENSG00000273706.4","gene_symbol":"LHX1","gene_name":"LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6593]","synonyms":"LIM1,LIM-1","biotype":"protein_coding","ncbi_id":"3975","summary":"This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor important for the development of the renal and urogenital systems. This gene is a candidate for Mayer-Rokitansky-Kuster-Hauser syndrome, a disorder characterized by anomalies in the female genital tract. [provided by RefSeq, Dec 2010]","start":36936785,"end":36944612,"strand":1,"description":"LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6593]"}, {"versioned_ensembl_gene_id":"ENSG00000102054.17","gene_symbol":"RBBP7","gene_name":"RB binding protein 7, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:9890]","synonyms":"RbAp46","biotype":"protein_coding","ncbi_id":"5931","summary":"This protein is a ubiquitously expressed nuclear protein and belongs to a highly conserved subfamily of WD-repeat proteins. It is found among several proteins that binds directly to retinoblastoma protein, which regulates cell proliferation. The encoded protein is found in many histone deacetylase complexes, including mSin3 co-repressor complex. It is also present in protein complexes involved in chromatin assembly. This protein can interact with BRCA1 tumor-suppressor gene and may have a role in the regulation of cell proliferation and differentiation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":16839283,"end":16870414,"strand":-1,"description":"RB binding protein 7, chromatin remodeling factor [Source:HGNC Symbol;Acc:HGNC:9890]"}, {"versioned_ensembl_gene_id":"ENSG00000105675.8","gene_symbol":"ATP4A","gene_name":"ATPase H+/K+ transporting alpha subunit [Source:HGNC Symbol;Acc:HGNC:819]","synonyms":"ATP6A","biotype":"protein_coding","ncbi_id":"495","summary":"The protein encoded by this gene belongs to a family of P-type cation-transporting ATPases. The gastric H+, K+-ATPase is a heterodimer consisting of a high molecular weight catalytic alpha subunit and a smaller but heavily glycosylated beta subunit. This enzyme is a proton pump that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for gastric acid secretion. This gene encodes a catalytic alpha subunit of the gastric H+, K+-ATPase. [provided by RefSeq, Jul 2008]","start":35550043,"end":35563658,"strand":-1,"description":"ATPase H+/K+ transporting alpha subunit [Source:HGNC Symbol;Acc:HGNC:819]"}, {"versioned_ensembl_gene_id":"ENSG00000283907.1","gene_symbol":"AD000090.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35557956,"end":35581954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272374.1","gene_symbol":"Z97832.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35220370,"end":35224630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230180.1","gene_symbol":"RPL12P49","gene_name":"ribosomal protein L12 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:51941]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075252","summary":null,"start":16803233,"end":16803353,"strand":1,"description":"ribosomal protein L12 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:51941]"}, {"versioned_ensembl_gene_id":"ENSG00000268670.1","gene_symbol":"AC016586.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4061615,"end":4062749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237877.6","gene_symbol":"LINC01473","gene_name":"long intergenic non-protein coding RNA 1473 [Source:HGNC Symbol;Acc:HGNC:51109]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927217","summary":null,"start":186032891,"end":186083233,"strand":-1,"description":"long intergenic non-protein coding RNA 1473 [Source:HGNC Symbol;Acc:HGNC:51109]"}, {"versioned_ensembl_gene_id":"ENSG00000271220.1","gene_symbol":"AL355376.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":28806121,"end":28813458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172578.11","gene_symbol":"KLHL6","gene_name":"kelch like family member 6 [Source:HGNC Symbol;Acc:HGNC:18653]","synonyms":"FLJ00029","biotype":"protein_coding","ncbi_id":"89857","summary":"This gene encodes a member of the kelch-like (KLHL) family of proteins, which is involved in B-lymphocyte antigen receptor signaling and germinal-center B-cell maturation. The encoded protein contains an N-terminal broad-complex, tramtrack and bric a brac (BTB) domain that facilitates protein binding and dimerization, a BTB and C-terminal kelch (BACK) domain, and six C-terminal kelch repeat domains. Naturally occurring mutations in this gene are associated with chronic lymphocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":183487531,"end":183555689,"strand":-1,"description":"kelch like family member 6 [Source:HGNC Symbol;Acc:HGNC:18653]"}, {"versioned_ensembl_gene_id":"ENSG00000242522.1","gene_symbol":"KLHL6-AS1","gene_name":"KLHL6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40850]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874019","summary":null,"start":183548735,"end":183552326,"strand":1,"description":"KLHL6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40850]"}, {"versioned_ensembl_gene_id":"ENSG00000204334.7","gene_symbol":"ERICH2","gene_name":"glutamate rich 2 [Source:HGNC Symbol;Acc:HGNC:44395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285141","summary":null,"start":170783786,"end":170798971,"strand":1,"description":"glutamate rich 2 [Source:HGNC Symbol;Acc:HGNC:44395]"}, {"versioned_ensembl_gene_id":"ENSG00000232624.6","gene_symbol":"LINC01517","gene_name":"long intergenic non-protein coding RNA 1517 [Source:HGNC Symbol;Acc:HGNC:51212]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101929218","summary":null,"start":28792668,"end":28808219,"strand":1,"description":"long intergenic non-protein coding RNA 1517 [Source:HGNC Symbol;Acc:HGNC:51212]"}, {"versioned_ensembl_gene_id":"ENSG00000236716.1","gene_symbol":"AL355376.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28743745,"end":28744663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167194.7","gene_symbol":"C16orf92","gene_name":"chromosome 16 open reading frame 92 [Source:HGNC Symbol;Acc:HGNC:26346]","synonyms":"FLJ25404","biotype":"protein_coding","ncbi_id":"146378","summary":null,"start":30023334,"end":30027736,"strand":1,"description":"chromosome 16 open reading frame 92 [Source:HGNC Symbol;Acc:HGNC:26346]"}, {"versioned_ensembl_gene_id":"ENSG00000224841.9","gene_symbol":"RGL2","gene_name":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]","synonyms":"KE1.5,HKE1.5,RAB2L","biotype":"protein_coding","ncbi_id":"5863","summary":null,"start":33213258,"end":33220928,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]"}, {"versioned_ensembl_gene_id":"ENSG00000125363.14","gene_symbol":"AMELX","gene_name":"amelogenin, X-linked [Source:HGNC Symbol;Acc:HGNC:461]","synonyms":"AIH1,AMG","biotype":"protein_coding","ncbi_id":"265","summary":"This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in this gene cause X-linked amelogenesis imperfecta. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":11293413,"end":11300761,"strand":1,"description":"amelogenin, X-linked [Source:HGNC Symbol;Acc:HGNC:461]"}, {"versioned_ensembl_gene_id":"ENSG00000206573.8","gene_symbol":"THUMPD3-AS1","gene_name":"THUMPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44478]","synonyms":"SETD5-AS1","biotype":"antisense_RNA","ncbi_id":"440944","summary":null,"start":9349689,"end":9398579,"strand":-1,"description":"THUMPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44478]"}, {"versioned_ensembl_gene_id":"ENSG00000282401.1","gene_symbol":"AC247036.3","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":106108743,"end":106109178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283338.1","gene_symbol":"AC090582.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":47323983,"end":47324181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254485.5","gene_symbol":"AC026191.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9292588,"end":9363303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231553.1","gene_symbol":"RNMTL1P1","gene_name":"RNA methyltransferase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44905]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420295","summary":null,"start":21394033,"end":21394592,"strand":1,"description":"RNA methyltransferase like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44905]"}, {"versioned_ensembl_gene_id":"ENSG00000232853.1","gene_symbol":"LUZP4P1","gene_name":"leucine zipper protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060111","summary":null,"start":21247752,"end":21248095,"strand":1,"description":"leucine zipper protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44904]"}, {"versioned_ensembl_gene_id":"ENSG00000149926.13","gene_symbol":"FAM57B","gene_name":"family with sequence similarity 57 member B [Source:HGNC Symbol;Acc:HGNC:25295]","synonyms":"DKFZP434I2117","biotype":"protein_coding","ncbi_id":"83723","summary":"This gene encodes a transmembrane protein, which may be a likely target of peroxisome proliferator-activated receptor gamma (PPAR-gamma). The product of the orthologous gene in mouse is related to obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30024427,"end":30052978,"strand":-1,"description":"family with sequence similarity 57 member B [Source:HGNC Symbol;Acc:HGNC:25295]"}, {"versioned_ensembl_gene_id":"ENSG00000260880.3","gene_symbol":"HCCAT5","gene_name":"hepatocellular carcinoma associated transcript 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48612]","synonyms":"FJ222407,HTA","biotype":"lincRNA","ncbi_id":"283902","summary":null,"start":73092349,"end":73099337,"strand":1,"description":"hepatocellular carcinoma associated transcript 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48612]"}, {"versioned_ensembl_gene_id":"ENSG00000196263.7","gene_symbol":"ZNF471","gene_name":"zinc finger protein 471 [Source:HGNC Symbol;Acc:HGNC:23226]","synonyms":"Z1971,KIAA1396","biotype":"protein_coding","ncbi_id":"57573","summary":null,"start":56507843,"end":56530221,"strand":1,"description":"zinc finger protein 471 [Source:HGNC Symbol;Acc:HGNC:23226]"}, {"versioned_ensembl_gene_id":"ENSG00000182621.17","gene_symbol":"PLCB1","gene_name":"phospholipase C beta 1 [Source:HGNC Symbol;Acc:HGNC:15917]","synonyms":"PLC154,PLC-I,KIAA0581","biotype":"protein_coding","ncbi_id":"23236","summary":"The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of many extracellular signals. This gene is activated by two G-protein alpha subunits, alpha-q and alpha-11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":8077251,"end":8968360,"strand":1,"description":"phospholipase C beta 1 [Source:HGNC Symbol;Acc:HGNC:15917]"}, {"versioned_ensembl_gene_id":"ENSG00000100101.15","gene_symbol":"Z83844.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":37686414,"end":37726503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171054.7","gene_symbol":"OR13H1","gene_name":"olfactory receptor family 13 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14755]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347468","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131544074,"end":131545000,"strand":1,"description":"olfactory receptor family 13 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14755]"}, {"versioned_ensembl_gene_id":"ENSG00000228438.1","gene_symbol":"AL445567.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8929895,"end":8930038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272691.1","gene_symbol":"AC092807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85578500,"end":85578742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147689.16","gene_symbol":"FAM83A","gene_name":"family with sequence similarity 83 member A [Source:HGNC Symbol;Acc:HGNC:28210]","synonyms":"MGC14128,BJ-TSA-9","biotype":"protein_coding","ncbi_id":"84985","summary":null,"start":123178960,"end":123210079,"strand":1,"description":"family with sequence similarity 83 member A [Source:HGNC Symbol;Acc:HGNC:28210]"}, {"versioned_ensembl_gene_id":"ENSG00000272031.2","gene_symbol":"ANKRD34A","gene_name":"ankyrin repeat domain 34A [Source:HGNC Symbol;Acc:HGNC:27639]","synonyms":"ANKRD34","biotype":"protein_coding","ncbi_id":"284615","summary":null,"start":145959442,"end":145964582,"strand":-1,"description":"ankyrin repeat domain 34A [Source:HGNC Symbol;Acc:HGNC:27639]"}, {"versioned_ensembl_gene_id":"ENSG00000238269.8","gene_symbol":"PAGE2B","gene_name":"PAGE family member 2B [Source:HGNC Symbol;Acc:HGNC:31805]","synonyms":"CT16.5","biotype":"protein_coding","ncbi_id":"389860","summary":null,"start":55075063,"end":55078909,"strand":1,"description":"PAGE family member 2B [Source:HGNC Symbol;Acc:HGNC:31805]"}, {"versioned_ensembl_gene_id":"ENSG00000253410.1","gene_symbol":"AC068228.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":123192875,"end":123192932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274299.1","gene_symbol":"AC099654.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57270839,"end":57275197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234089.1","gene_symbol":"AC099654.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57209865,"end":57222174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240771.6","gene_symbol":"ARHGEF25","gene_name":"Rho guanine nucleotide exchange factor 25 [Source:HGNC Symbol;Acc:HGNC:30275]","synonyms":"p63RhoGEF,GEFT","biotype":"protein_coding","ncbi_id":"115557","summary":"Rho GTPases alternate between an inactive GDP-bound state and an active GTP-bound state, and GEFs facilitate GDP/GTP exchange. This gene encodes a guanine nucleotide exchange factor (GEF) which interacts with Rho GTPases involved in contraction of vascular smooth muscles, regulation of responses to angiotensin II and lens cell differentiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":57610180,"end":57619379,"strand":1,"description":"Rho guanine nucleotide exchange factor 25 [Source:HGNC Symbol;Acc:HGNC:30275]"}, {"versioned_ensembl_gene_id":"ENSG00000276920.4","gene_symbol":"NKD2","gene_name":"naked cuticle homolog 2 [Source:HGNC Symbol;Acc:HGNC:17046]","synonyms":"Naked2","biotype":"protein_coding","ncbi_id":"85409","summary":"This gene encodes a member of a family of proteins that function as negative regulators of Wnt receptor signaling through interaction with Dishevelled family members. The encoded protein participates in the delivery of transforming growth factor alpha-containing vesicles to the cell membrane. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":1008829,"end":1038943,"strand":1,"description":"naked cuticle homolog 2 [Source:HGNC Symbol;Acc:HGNC:17046]"}, {"versioned_ensembl_gene_id":"ENSG00000236179.1","gene_symbol":"PRAMEF35P","gene_name":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419649","summary":null,"start":13104403,"end":13105689,"strand":-1,"description":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]"}, {"versioned_ensembl_gene_id":"ENSG00000259974.2","gene_symbol":"LINC00261","gene_name":"long intergenic non-protein coding RNA 261 [Source:HGNC Symbol;Acc:HGNC:16189]","synonyms":"NCRNA00261,HCCDR1,DEANR1,C20orf56,bA216C10.1,ALIEN,TCONS_00027846,onco-lncRNA-17","biotype":"lincRNA","ncbi_id":"140828","summary":"This gene produces a long non-coding RNA that acts as a negative regulator of cell growth. This transcript may promote differentiation and apoptosis. [provided by RefSeq, Dec 2017]","start":22547671,"end":22578642,"strand":-1,"description":"long intergenic non-protein coding RNA 261 [Source:HGNC Symbol;Acc:HGNC:16189]"}, {"versioned_ensembl_gene_id":"ENSG00000229182.3","gene_symbol":"MRPS16P1","gene_name":"mitochondrial ribosomal protein S16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"137406","summary":null,"start":91917507,"end":91917918,"strand":1,"description":"mitochondrial ribosomal protein S16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29732]"}, {"versioned_ensembl_gene_id":"ENSG00000284723.1","gene_symbol":"OR8S1","gene_name":"olfactory receptor family 8 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:19628]","synonyms":null,"biotype":"protein_coding","ncbi_id":"341568","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48525632,"end":48528103,"strand":1,"description":"olfactory receptor family 8 subfamily S member 1 [Source:HGNC Symbol;Acc:HGNC:19628]"}, {"versioned_ensembl_gene_id":"ENSG00000112759.16","gene_symbol":"SLC29A1","gene_name":"solute carrier family 29 member 1 (Augustine blood group) [Source:HGNC Symbol;Acc:HGNC:11003]","synonyms":"ENT1","biotype":"protein_coding","ncbi_id":"2030","summary":"This gene is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides used for cancer and viral chemotherapies. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]","start":44219505,"end":44234151,"strand":1,"description":"solute carrier family 29 member 1 (Augustine blood group) [Source:HGNC Symbol;Acc:HGNC:11003]"}, {"versioned_ensembl_gene_id":"ENSG00000100889.11","gene_symbol":"PCK2","gene_name":"phosphoenolpyruvate carboxykinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:8725]","synonyms":"PEPCK,PEPCK2","biotype":"protein_coding","ncbi_id":"5106","summary":"This gene encodes a mitochondrial enzyme that catalyzes the conversion of oxaloacetate to phosphoenolpyruvate in the presence of guanosine triphosphate (GTP). A cytosolic form of this protein is encoded by a different gene and is the key enzyme of gluconeogenesis in the liver. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2014]","start":24094053,"end":24110598,"strand":1,"description":"phosphoenolpyruvate carboxykinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:8725]"}, {"versioned_ensembl_gene_id":"ENSG00000105176.17","gene_symbol":"URI1","gene_name":"URI1, prefoldin like chaperone [Source:HGNC Symbol;Acc:HGNC:13236]","synonyms":"URI,RMP,PPP1R19,NNX3,FLJ10575,C19orf2","biotype":"protein_coding","ncbi_id":"8725","summary":"This gene encodes member of the prefoldin family of molecular chaperones. The encoded protein functions as a scaffolding protein and plays roles in ubiquitination and transcription, in part though interactions with the RNA polymerase II subunit RPB5. This gene may play a role in multiple malignancies including ovarian cancer and hepatocellular carcinoma. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 22. [provided by RefSeq, Nov 2011]","start":29923644,"end":30016608,"strand":1,"description":"URI1, prefoldin like chaperone [Source:HGNC Symbol;Acc:HGNC:13236]"}, {"versioned_ensembl_gene_id":"ENSG00000223414.2","gene_symbol":"LINC00473","gene_name":"long intergenic non-protein coding RNA 473 [Source:HGNC Symbol;Acc:HGNC:21160]","synonyms":"C6orf176,bA142J11.1","biotype":"lincRNA","ncbi_id":"90632","summary":null,"start":165908802,"end":165988048,"strand":-1,"description":"long intergenic non-protein coding RNA 473 [Source:HGNC Symbol;Acc:HGNC:21160]"}, {"versioned_ensembl_gene_id":"ENSG00000261392.1","gene_symbol":"AC087190.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9068554,"end":9072412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281832.1","gene_symbol":"LINC00602","gene_name":"long intergenic non-protein coding RNA 602 [Source:HGNC Symbol;Acc:HGNC:43917]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441177","summary":null,"start":165987551,"end":165989615,"strand":1,"description":"long intergenic non-protein coding RNA 602 [Source:HGNC Symbol;Acc:HGNC:43917]"}, {"versioned_ensembl_gene_id":"ENSG00000236627.1","gene_symbol":"AL590302.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165754189,"end":165775780,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223942.1","gene_symbol":"AL590302.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":165773201,"end":165775186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238217.5","gene_symbol":"LINC01877","gene_name":"long intergenic non-protein coding RNA 1877 [Source:HGNC Symbol;Acc:HGNC:52696]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927641","summary":null,"start":199608068,"end":199659132,"strand":1,"description":"long intergenic non-protein coding RNA 1877 [Source:HGNC Symbol;Acc:HGNC:52696]"}, {"versioned_ensembl_gene_id":"ENSG00000143127.12","gene_symbol":"ITGA10","gene_name":"integrin subunit alpha 10 [Source:HGNC Symbol;Acc:HGNC:6135]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8515","summary":"Integrins are integral transmembrane glycoproteins composed of noncovalently linked alpha and beta chains. They participate in cell adhesion as well as cell-surface mediated signalling. This gene encodes an integrin alpha chain and is expressed at high levels in chondrocytes, where it is transcriptionally regulated by AP-2epsilon and Ets-1. The protein encoded by this gene binds to collagen. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":145891208,"end":145910189,"strand":-1,"description":"integrin subunit alpha 10 [Source:HGNC Symbol;Acc:HGNC:6135]"}, {"versioned_ensembl_gene_id":"ENSG00000270889.1","gene_symbol":"AC087072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35971147,"end":35971567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274178.2","gene_symbol":"PRAMEF28P","gene_name":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]","synonyms":"PRAMEF28","biotype":"unprocessed_pseudogene","ncbi_id":"102724742","summary":null,"start":13029339,"end":13032130,"strand":1,"description":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]"}, {"versioned_ensembl_gene_id":"ENSG00000173825.6","gene_symbol":"TIGD3","gene_name":"tigger transposable element derived 3 [Source:HGNC Symbol;Acc:HGNC:18334]","synonyms":null,"biotype":"protein_coding","ncbi_id":"220359","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":65354767,"end":65357613,"strand":1,"description":"tigger transposable element derived 3 [Source:HGNC Symbol;Acc:HGNC:18334]"}, {"versioned_ensembl_gene_id":"ENSG00000135148.11","gene_symbol":"TRAFD1","gene_name":"TRAF-type zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24808]","synonyms":"FLN29","biotype":"protein_coding","ncbi_id":"10906","summary":"The innate immune system confers host defense against viral and microbial infection, and TRAFD1 is a negative feedback regulator that controls excessive immune responses (Sanada et al., 2008 [PubMed 18849341]).[supplied by OMIM, Dec 2009]","start":112125501,"end":112153609,"strand":1,"description":"TRAF-type zinc finger domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24808]"}, {"versioned_ensembl_gene_id":"ENSG00000281922.1","gene_symbol":"AC139677.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46784842,"end":46785913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281336.1","gene_symbol":"AC139677.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46769907,"end":46770900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278535.4","gene_symbol":"DHRS11","gene_name":"dehydrogenase/reductase 11 [Source:HGNC Symbol;Acc:HGNC:28639]","synonyms":"MGC4172,SDR24C1","biotype":"protein_coding","ncbi_id":"79154","summary":null,"start":36591798,"end":36600806,"strand":1,"description":"dehydrogenase/reductase 11 [Source:HGNC Symbol;Acc:HGNC:28639]"}, {"versioned_ensembl_gene_id":"ENSG00000149050.9","gene_symbol":"ZNF214","gene_name":"zinc finger protein 214 [Source:HGNC Symbol;Acc:HGNC:13006]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7761","summary":"This gene is expressed predominantly in the testis and encodes a zinc finger protein that contains an N-terminal kruppel-associated box A (KRABA) domain and twelve zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017]","start":6999318,"end":7020368,"strand":-1,"description":"zinc finger protein 214 [Source:HGNC Symbol;Acc:HGNC:13006]"}, {"versioned_ensembl_gene_id":"ENSG00000121680.15","gene_symbol":"PEX16","gene_name":"peroxisomal biogenesis factor 16 [Source:HGNC Symbol;Acc:HGNC:8857]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9409","summary":"The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008]","start":45909669,"end":45918812,"strand":-1,"description":"peroxisomal biogenesis factor 16 [Source:HGNC Symbol;Acc:HGNC:8857]"}, {"versioned_ensembl_gene_id":"ENSG00000249096.6","gene_symbol":"LINC02362","gene_name":"long intergenic non-protein coding RNA 2362 [Source:HGNC Symbol;Acc:HGNC:53284]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723766","summary":null,"start":184365183,"end":184382306,"strand":-1,"description":"long intergenic non-protein coding RNA 2362 [Source:HGNC Symbol;Acc:HGNC:53284]"}, {"versioned_ensembl_gene_id":"ENSG00000241695.1","gene_symbol":"GM2AP1","gene_name":"GM2 ganglioside activator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4368]","synonyms":"GM2AP","biotype":"processed_pseudogene","ncbi_id":"2761","summary":null,"start":145684572,"end":145685092,"strand":1,"description":"GM2 ganglioside activator pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4368]"}, {"versioned_ensembl_gene_id":"ENSG00000254838.5","gene_symbol":"GVINP1","gene_name":"GTPase, very large interferon inducible pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25813]","synonyms":"VLIG1,VLIG-1,GVIN1P,GVIN1,FLJ13373","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"387751","summary":null,"start":6713536,"end":6746439,"strand":-1,"description":"GTPase, very large interferon inducible pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25813]"}, {"versioned_ensembl_gene_id":"ENSG00000103657.13","gene_symbol":"HERC1","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 [Source:HGNC Symbol;Acc:HGNC:4867]","synonyms":"p532,p619","biotype":"protein_coding","ncbi_id":"8925","summary":"This gen encodes a member of the HERC protein family. This protein stimulates guanine nucleotide exchange on ARF1 and Rab proteins. This protein may be involved in membrane transport processes. [provided by RefSeq, Mar 2012]","start":63608618,"end":63833942,"strand":-1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 [Source:HGNC Symbol;Acc:HGNC:4867]"}, {"versioned_ensembl_gene_id":"ENSG00000278928.1","gene_symbol":"AC136621.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":55704119,"end":55706422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226266.6","gene_symbol":"AC009961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159670708,"end":159712435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230783.1","gene_symbol":"AC009961.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159689217,"end":159690291,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107372.12","gene_symbol":"ZFAND5","gene_name":"zinc finger AN1-type containing 5 [Source:HGNC Symbol;Acc:HGNC:13008]","synonyms":"ZNF216,ZFAND5A,ZA20D2","biotype":"protein_coding","ncbi_id":"7763","summary":null,"start":72351425,"end":72365235,"strand":-1,"description":"zinc finger AN1-type containing 5 [Source:HGNC Symbol;Acc:HGNC:13008]"}, {"versioned_ensembl_gene_id":"ENSG00000236153.1","gene_symbol":"AC104076.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":180979427,"end":180980090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122884.12","gene_symbol":"P4HA1","gene_name":"prolyl 4-hydroxylase subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:8546]","synonyms":"P4HA,C-P4Halpha(I)","biotype":"protein_coding","ncbi_id":"5033","summary":"This gene encodes a component of prolyl 4-hydroxylase, a key enzyme in collagen synthesis composed of two identical alpha subunits and two beta subunits. The encoded protein is one of several different types of alpha subunits and provides the major part of the catalytic site of the active enzyme. In collagen and related proteins, prolyl 4-hydroxylase catalyzes the formation of 4-hydroxyproline that is essential to the proper three-dimensional folding of newly synthesized procollagen chains. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":73007217,"end":73096974,"strand":-1,"description":"prolyl 4-hydroxylase subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:8546]"}, {"versioned_ensembl_gene_id":"ENSG00000231890.7","gene_symbol":"DARS-AS1","gene_name":"DARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40170]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928243","summary":null,"start":135985176,"end":136022593,"strand":1,"description":"DARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40170]"}, {"versioned_ensembl_gene_id":"ENSG00000182782.7","gene_symbol":"HCAR2","gene_name":"hydroxycarboxylic acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:24827]","synonyms":"PUMAG,Puma-g,NIACR1,HM74A,HCA2,GPR109A","biotype":"protein_coding","ncbi_id":"338442","summary":null,"start":122701293,"end":122703343,"strand":-1,"description":"hydroxycarboxylic acid receptor 2 [Source:HGNC Symbol;Acc:HGNC:24827]"}, {"versioned_ensembl_gene_id":"ENSG00000233529.1","gene_symbol":"HCG21","gene_name":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]","synonyms":"NCRNA00150,AB023048.2","biotype":"antisense_RNA","ncbi_id":"102723346","summary":null,"start":30945979,"end":30954862,"strand":-1,"description":"HLA complex group 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31335]"}, {"versioned_ensembl_gene_id":"ENSG00000230143.9","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30719960,"end":30734994,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000275400.1","gene_symbol":"AC006001.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66553805,"end":66554199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215472.10","gene_symbol":"RPL17-C18orf32","gene_name":"RPL17-C18orf32 readthrough [Source:HGNC Symbol;Acc:HGNC:44661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526842","summary":"This locus represents naturally occurring read-through transcription between the neighboring RPL17 (ribosomal protein L17) and C18orf32 (chromosome 18 open reading frame 32) genes. Alternative splicing results in multiple transcript variants. The encoded isoforms share sequence identity with the RPL17 protein, but they include frameshifted C-terminal regions derived from the downstream gene exons. [provided by RefSeq, Dec 2010]","start":49481681,"end":49492479,"strand":-1,"description":"RPL17-C18orf32 readthrough [Source:HGNC Symbol;Acc:HGNC:44661]"}, {"versioned_ensembl_gene_id":"ENSG00000277690.2","gene_symbol":"AC023490.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18527157,"end":18527626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282550.1","gene_symbol":"IGHV1-2","gene_name":"immunoglobulin heavy variable 1-2 [Source:HGNC Symbol;Acc:HGNC:5550]","synonyms":"V35","biotype":"IG_V_gene","ncbi_id":"28474","summary":null,"start":105987353,"end":105987854,"strand":-1,"description":"immunoglobulin heavy variable 1-2 [Source:HGNC Symbol;Acc:HGNC:5550]"}, {"versioned_ensembl_gene_id":"ENSG00000226969.1","gene_symbol":"AL391845.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2049203,"end":2050070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237310.1","gene_symbol":"GS1-124K5.4","gene_name":"uncharacterized LOC100289098 [Source:NCBI gene;Acc:100289098]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100289098","summary":null,"start":66493706,"end":66495474,"strand":1,"description":"uncharacterized LOC100289098 [Source:NCBI gene;Acc:100289098]"}, {"versioned_ensembl_gene_id":"ENSG00000277017.1","gene_symbol":"AC023490.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18486999,"end":18491247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230927.3","gene_symbol":"TMBIM7P","gene_name":"transmembrane BAX inhibitor motif containing 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:49212]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"105375396","summary":null,"start":92412550,"end":92447813,"strand":-1,"description":"transmembrane BAX inhibitor motif containing 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:49212]"}, {"versioned_ensembl_gene_id":"ENSG00000283383.1","gene_symbol":"AC108477.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183762115,"end":183765721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000004961.14","gene_symbol":"HCCS","gene_name":"holocytochrome c synthase [Source:HGNC Symbol;Acc:HGNC:4837]","synonyms":"MLS,CCHL","biotype":"protein_coding","ncbi_id":"3052","summary":"The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]","start":11111301,"end":11123078,"strand":1,"description":"holocytochrome c synthase [Source:HGNC Symbol;Acc:HGNC:4837]"}, {"versioned_ensembl_gene_id":"ENSG00000257642.1","gene_symbol":"KCCAT198","gene_name":"renal clear cell carcinoma-associated transcript 198 [Source:NCBI gene;Acc:105369954]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105369954","summary":null,"start":105304867,"end":105327017,"strand":-1,"description":"renal clear cell carcinoma-associated transcript 198 [Source:NCBI gene;Acc:105369954]"}, {"versioned_ensembl_gene_id":"ENSG00000255366.1","gene_symbol":"AC120036.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47190772,"end":47193262,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213700.3","gene_symbol":"RPL17P50","gene_name":"ribosomal protein L17 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45098]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729046","summary":null,"start":73005833,"end":73006595,"strand":-1,"description":"ribosomal protein L17 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45098]"}, {"versioned_ensembl_gene_id":"ENSG00000248531.3","gene_symbol":"NDUFA5P12","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48854]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288013","summary":null,"start":47164870,"end":47165524,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48854]"}, {"versioned_ensembl_gene_id":"ENSG00000242073.2","gene_symbol":"AC211429.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75474707,"end":75486108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232169.9","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"ABC50,EST123147","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30561610,"end":30587416,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000280092.1","gene_symbol":"AC002044.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73005601,"end":73006141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177425.10","gene_symbol":"PAWR","gene_name":"pro-apoptotic WT1 regulator [Source:HGNC Symbol;Acc:HGNC:8614]","synonyms":"par-4,PAR4","biotype":"protein_coding","ncbi_id":"5074","summary":"This gene encodes a tumor suppressor protein that selectively induces apoptosis in cancer cells through intracellular and extracellular mechanisms. The intracellular mechanism involves the inhibition of pro-survival pathways and the activation of Fas-mediated apoptosis, while the extracellular mechanism involves the binding of a secreted form of this protein to glucose regulated protein 78 (GRP78) on the cell surface, which leads to activation of the extrinsic apoptotic pathway. This gene is located on the unstable human chromosomal 12q21 region and is often deleted or mutated different tumors. The encoded protein also plays an important role in the progression of age-related diseases. [provided by RefSeq, Aug 2017]","start":79574979,"end":79691097,"strand":-1,"description":"pro-apoptotic WT1 regulator [Source:HGNC Symbol;Acc:HGNC:8614]"}, {"versioned_ensembl_gene_id":"ENSG00000261787.1","gene_symbol":"TCF24","gene_name":"transcription factor 24 [Source:HGNC Symbol;Acc:HGNC:32275]","synonyms":"bHLHa25","biotype":"protein_coding","ncbi_id":"100129654","summary":null,"start":66946501,"end":66962590,"strand":-1,"description":"transcription factor 24 [Source:HGNC Symbol;Acc:HGNC:32275]"}, {"versioned_ensembl_gene_id":"ENSG00000241947.1","gene_symbol":"HNRNPA1P24","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874396","summary":null,"start":149999645,"end":150000690,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39542]"}, {"versioned_ensembl_gene_id":"ENSG00000140836.15","gene_symbol":"ZFHX3","gene_name":"zinc finger homeobox 3 [Source:HGNC Symbol;Acc:HGNC:777]","synonyms":"ZNF927,ATBF1","biotype":"protein_coding","ncbi_id":"463","summary":"This gene encodes a transcription factor with multiple homeodomains and zinc finger motifs, and regulates myogenic and neuronal differentiation. The encoded protein suppresses expression of the alpha-fetoprotein gene by binding to an AT-rich enhancer motif. The protein has also been shown to negatively regulate c-Myb, and transactivate the cell cycle inhibitor cyclin-dependent kinase inhibitor 1A (also known as p21CIP1). This gene is reported to function as a tumor suppressor in several cancers, and sequence variants of this gene are also associated with atrial fibrillation. Multiple transcript variants expressed from alternate promoters and encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":72782885,"end":73144447,"strand":-1,"description":"zinc finger homeobox 3 [Source:HGNC Symbol;Acc:HGNC:777]"}, {"versioned_ensembl_gene_id":"ENSG00000182035.11","gene_symbol":"ADIG","gene_name":"adipogenin [Source:HGNC Symbol;Acc:HGNC:28606]","synonyms":"SMAF1,RP5-1100H13.2,MGC39724","biotype":"protein_coding","ncbi_id":"149685","summary":"ADIG/SMAF1 is an adipocyte-specific protein that plays a role in adipocyte differentiation (Kim et al., 2005 [PubMed 15567149]; Hong et al., 2005 [PubMed 16132694]).[supplied by OMIM, Mar 2008]","start":38581195,"end":38588463,"strand":1,"description":"adipogenin [Source:HGNC Symbol;Acc:HGNC:28606]"}, {"versioned_ensembl_gene_id":"ENSG00000183873.15","gene_symbol":"SCN5A","gene_name":"sodium voltage-gated channel alpha subunit 5 [Source:HGNC Symbol;Acc:HGNC:10593]","synonyms":"CMD1E,LQT3,CDCD2,IVF,ICCD,HH1,HBBD,HB2,SSS1,HB1,PFHB1,CMPD2,Nav1.5","biotype":"protein_coding","ncbi_id":"6331","summary":"The protein encoded by this gene is an integral membrane protein and tetrodotoxin-resistant voltage-gated sodium channel subunit. This protein is found primarily in cardiac muscle and is responsible for the initial upstroke of the action potential in an electrocardiogram. Defects in this gene are a cause of long QT syndrome type 3 (LQT3), an autosomal dominant cardiac disease. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":38548057,"end":38649673,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 5 [Source:HGNC Symbol;Acc:HGNC:10593]"}, {"versioned_ensembl_gene_id":"ENSG00000139351.14","gene_symbol":"SYCP3","gene_name":"synaptonemal complex protein 3 [Source:HGNC Symbol;Acc:HGNC:18130]","synonyms":null,"biotype":"protein_coding","ncbi_id":"50511","summary":"This gene encodes an essential structural component of the synaptonemal complex. This complex is involved in synapsis, recombination and segregation of meiotic chromosomes. Mutations in this gene are associated with azoospermia in males and susceptibility to pregnancy loss in females. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2010]","start":101728648,"end":101739472,"strand":-1,"description":"synaptonemal complex protein 3 [Source:HGNC Symbol;Acc:HGNC:18130]"}, {"versioned_ensembl_gene_id":"ENSG00000243944.5","gene_symbol":"AC117386.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150039214,"end":150213726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184979.9","gene_symbol":"USP18","gene_name":"ubiquitin specific peptidase 18 [Source:HGNC Symbol;Acc:HGNC:12616]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11274","summary":"The protein encoded by this gene belongs to the ubiquitin-specific proteases (UBP) family of enzymes that cleave ubiquitin from ubiquitinated protein substrates. It is highly expressed in liver and thymus, and is localized to the nucleus. This protein efficiently cleaves only ISG15 (a ubiquitin-like protein) fusions, and deletion of this gene in mice results in a massive increase of ISG15 conjugates in tissues, indicating that this protein is a major ISG15-specific protease. Mice lacking this gene are also hypersensitive to interferon, suggesting a function of this protein in downregulating interferon responses, independent of its isopeptidase activity towards ISG15. [provided by RefSeq, Sep 2011]","start":18149899,"end":18177397,"strand":1,"description":"ubiquitin specific peptidase 18 [Source:HGNC Symbol;Acc:HGNC:12616]"}, {"versioned_ensembl_gene_id":"ENSG00000259955.1","gene_symbol":"AC008741.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25238318,"end":25239287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230112.1","gene_symbol":"AL157398.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20841375,"end":20841560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253408.5","gene_symbol":"AC083973.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42233675,"end":42271197,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000082397.17","gene_symbol":"EPB41L3","gene_name":"erythrocyte membrane protein band 4.1 like 3 [Source:HGNC Symbol;Acc:HGNC:3380]","synonyms":"KIAA0987,DAL1,4.1B","biotype":"protein_coding","ncbi_id":"23136","summary":null,"start":5392381,"end":5630700,"strand":-1,"description":"erythrocyte membrane protein band 4.1 like 3 [Source:HGNC Symbol;Acc:HGNC:3380]"}, {"versioned_ensembl_gene_id":"ENSG00000174740.7","gene_symbol":"PABPC5","gene_name":"poly(A) binding protein cytoplasmic 5 [Source:HGNC Symbol;Acc:HGNC:13629]","synonyms":"PABP5","biotype":"protein_coding","ncbi_id":"140886","summary":"This gene encodes a protein that binds to the polyA tail found at the 3' end of most eukaryotic mRNAs. It is thought to play a role in the regulation of mRNA metabolic processes in the cytoplasm. This gene is located in a gene-poor region within the X-specific 13d-sY43 subinterval of the chromosome Xq21.3/Yp11.2 homology block. It is located close to translocation breakpoints associated with premature ovarian failure, and is therefore a potential candidate gene for this disorder. [provided by RefSeq, May 2010]","start":91434595,"end":91438584,"strand":1,"description":"poly(A) binding protein cytoplasmic 5 [Source:HGNC Symbol;Acc:HGNC:13629]"}, {"versioned_ensembl_gene_id":"ENSG00000224880.1","gene_symbol":"MTCYBP29","gene_name":"mitochondrially encoded cytochrome b pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:51995]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075135","summary":null,"start":57173357,"end":57174362,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:51995]"}, {"versioned_ensembl_gene_id":"ENSG00000274022.1","gene_symbol":"AL121873.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":90208895,"end":90209418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236980.9","gene_symbol":"C3orf84","gene_name":"chromosome 3 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:44666]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646498","summary":null,"start":49177632,"end":49191858,"strand":-1,"description":"chromosome 3 open reading frame 84 [Source:HGNC Symbol;Acc:HGNC:44666]"}, {"versioned_ensembl_gene_id":"ENSG00000237824.2","gene_symbol":"RPL23AP33","gene_name":"ribosomal protein L23a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36946]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271293","summary":null,"start":184902111,"end":184902562,"strand":-1,"description":"ribosomal protein L23a pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36946]"}, {"versioned_ensembl_gene_id":"ENSG00000234172.1","gene_symbol":"AC093639.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":183904529,"end":183949112,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177855.8","gene_symbol":"CACYBPP2","gene_name":"calcyclin binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45123]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644877","summary":null,"start":183607442,"end":183608119,"strand":-1,"description":"calcyclin binding protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45123]"}, {"versioned_ensembl_gene_id":"ENSG00000228753.1","gene_symbol":"EIF4BP2","gene_name":"eukaryotic translation initiation factor 4B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129337","summary":null,"start":21028999,"end":21030792,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37935]"}, {"versioned_ensembl_gene_id":"ENSG00000281407.1","gene_symbol":"FAM90A22P","gene_name":"family with sequence similarity 90 member A22, pseudogene [Source:HGNC Symbol;Acc:HGNC:32270]","synonyms":"FAM90A22","biotype":"unprocessed_pseudogene","ncbi_id":"645558","summary":null,"start":7563971,"end":7566982,"strand":-1,"description":"family with sequence similarity 90 member A22, pseudogene [Source:HGNC Symbol;Acc:HGNC:32270]"}, {"versioned_ensembl_gene_id":"ENSG00000281040.1","gene_symbol":"FAM90A7P","gene_name":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]","synonyms":"FAM90A7","biotype":"unprocessed_pseudogene","ncbi_id":"441317","summary":"FAM90A7 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7548676,"end":7551688,"strand":-1,"description":"family with sequence similarity 90 member A7, pseudogene [Source:HGNC Symbol;Acc:HGNC:32255]"}, {"versioned_ensembl_gene_id":"ENSG00000230072.2","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":30975998,"end":30976820,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000250148.1","gene_symbol":"KRT8P31","gene_name":"keratin 8 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39865]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728167","summary":null,"start":60743563,"end":60744970,"strand":-1,"description":"keratin 8 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39865]"}, {"versioned_ensembl_gene_id":"ENSG00000237114.2","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31160057,"end":31165363,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000231307.1","gene_symbol":"RPS3P2","gene_name":"ribosomal protein S3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16603]","synonyms":"dJ927M24.3","biotype":"processed_pseudogene","ncbi_id":"140761","summary":null,"start":38537758,"end":38538458,"strand":1,"description":"ribosomal protein S3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16603]"}, {"versioned_ensembl_gene_id":"ENSG00000264016.2","gene_symbol":"AC015908.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10741267,"end":10769016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243759.1","gene_symbol":"ST13P15","gene_name":"ST13, Hsp70 interacting protein pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38850]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422603","summary":null,"start":143517123,"end":143518229,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38850]"}, {"versioned_ensembl_gene_id":"ENSG00000280916.1","gene_symbol":"FOXCUT","gene_name":"FOXC1 upstream transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50650]","synonyms":"TCONS_00011636,LINC01379","biotype":"lincRNA","ncbi_id":"101927703","summary":null,"start":1605531,"end":1606079,"strand":1,"description":"FOXC1 upstream transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50650]"}, {"versioned_ensembl_gene_id":"ENSG00000228345.2","gene_symbol":"AC112492.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27854323,"end":27855353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000033050.7","gene_symbol":"ABCF2","gene_name":"ATP binding cassette subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:71]","synonyms":"M-ABC1,HUSSY-18,EST133090,ABC28","biotype":"protein_coding","ncbi_id":"10061","summary":"This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ATP-binding cassette proteins transport various molecules across extra- and intracellular membranes. Alterations in this gene may be involved in cancer progression. Related pseudogenes have been identified on chromosomes 3 and 7. [provided by RefSeq, Mar 2019]","start":151207837,"end":151227230,"strand":-1,"description":"ATP binding cassette subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:71]"}, {"versioned_ensembl_gene_id":"ENSG00000224305.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32679790,"end":32687227,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000281351.1","gene_symbol":"SUDS3P1","gene_name":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285647","summary":null,"start":177971313,"end":177972279,"strand":1,"description":"SDS3 homolog, SIN3A corepressor complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44000]"}, {"versioned_ensembl_gene_id":"ENSG00000187288.10","gene_symbol":"CIDEC","gene_name":"cell death inducing DFFA like effector c [Source:HGNC Symbol;Acc:HGNC:24229]","synonyms":"Fsp27,FLJ20871,CIDE-3","biotype":"protein_coding","ncbi_id":"63924","summary":"This gene encodes a member of the cell death-inducing DNA fragmentation factor-like effector family. Members of this family play important roles in apoptosis. The encoded protein promotes lipid droplet formation in adipocytes and may mediate adipocyte apoptosis. This gene is regulated by insulin and its expression is positively correlated with insulin sensitivity. Mutations in this gene may contribute to insulin resistant diabetes. A pseudogene of this gene is located on the short arm of chromosome 3. Alternatively spliced transcript variants that encode different isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":9866711,"end":9880254,"strand":-1,"description":"cell death inducing DFFA like effector c [Source:HGNC Symbol;Acc:HGNC:24229]"}, {"versioned_ensembl_gene_id":"ENSG00000281644.2","gene_symbol":"AC106795.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177950335,"end":177963960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270441.1","gene_symbol":"AC135506.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49140086,"end":49160851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237889.11","gene_symbol":"DDX39B","gene_name":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]","synonyms":"BAT1,UAP56,D6S81E","biotype":"protein_coding","ncbi_id":"7919","summary":"This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]","start":31597175,"end":31606140,"strand":-1,"description":"DExD-box helicase 39B [Source:HGNC Symbol;Acc:HGNC:13917]"}, {"versioned_ensembl_gene_id":"ENSG00000282190.1","gene_symbol":"AC243660.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28475678,"end":28478612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203327.2","gene_symbol":"AC012358.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55214387,"end":55216126,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275794.2","gene_symbol":"DEFB106B","gene_name":"defensin beta 106B [Source:HGNC Symbol;Acc:HGNC:28879]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503841","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 106, DEFB106A and DEFB106B, in head-to-head orientation. This gene, DEFB106B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7474484,"end":7478378,"strand":-1,"description":"defensin beta 106B [Source:HGNC Symbol;Acc:HGNC:28879]"}, {"versioned_ensembl_gene_id":"ENSG00000115163.14","gene_symbol":"CENPA","gene_name":"centromere protein A [Source:HGNC Symbol;Acc:HGNC:1851]","synonyms":"CENP-A,CenH3","biotype":"protein_coding","ncbi_id":"1058","summary":"Centromeres are the differentiated chromosomal domains that specify the mitotic behavior of chromosomes. This gene encodes a centromere protein which contains a histone H3 related histone fold domain that is required for targeting to the centromere. Centromere protein A is proposed to be a component of a modified nucleosome or nucleosome-like structure in which it replaces 1 or both copies of conventional histone H3 in the (H3-H4)2 tetrameric core of the nucleosome particle. The protein is a replication-independent histone that is a member of the histone H3 family. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2015]","start":26764289,"end":26801067,"strand":1,"description":"centromere protein A [Source:HGNC Symbol;Acc:HGNC:1851]"}, {"versioned_ensembl_gene_id":"ENSG00000066279.17","gene_symbol":"ASPM","gene_name":"abnormal spindle microtubule assembly [Source:HGNC Symbol;Acc:HGNC:19048]","synonyms":"MCPH5,FLJ10549,FLJ10517,Calmbp1,ASP","biotype":"protein_coding","ncbi_id":"259266","summary":"This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":197084128,"end":197146694,"strand":-1,"description":"abnormal spindle microtubule assembly [Source:HGNC Symbol;Acc:HGNC:19048]"}, {"versioned_ensembl_gene_id":"ENSG00000283311.1","gene_symbol":"AC099654.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57172772,"end":57173283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118640.10","gene_symbol":"VAMP8","gene_name":"vesicle associated membrane protein 8 [Source:HGNC Symbol;Acc:HGNC:12647]","synonyms":"EDB","biotype":"protein_coding","ncbi_id":"8673","summary":"This gene encodes an integral membrane protein that belongs to the synaptobrevin/vesicle-associated membrane protein subfamily of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs). The encoded protein is involved in the fusion of synaptic vesicles with the presynaptic membrane.[provided by RefSeq, Jun 2010]","start":85561562,"end":85582031,"strand":1,"description":"vesicle associated membrane protein 8 [Source:HGNC Symbol;Acc:HGNC:12647]"}, {"versioned_ensembl_gene_id":"ENSG00000095587.8","gene_symbol":"TLL2","gene_name":"tolloid like 2 [Source:HGNC Symbol;Acc:HGNC:11844]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7093","summary":"This gene encodes an astacin-like zinc-dependent metalloprotease and is a subfamily member of the metzincin family. Unlike other family members, a similar protein in mice does not cleave procollagen C-propeptides or chordin. [provided by RefSeq, Jul 2008]","start":96364606,"end":96513918,"strand":-1,"description":"tolloid like 2 [Source:HGNC Symbol;Acc:HGNC:11844]"}, {"versioned_ensembl_gene_id":"ENSG00000270015.1","gene_symbol":"AC087481.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30926514,"end":30928407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251155.2","gene_symbol":"SEPT14P4","gene_name":"septin 14 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51688]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107105266","summary":null,"start":118640673,"end":118640858,"strand":1,"description":"septin 14 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51688]"}, {"versioned_ensembl_gene_id":"ENSG00000270575.1","gene_symbol":"AL160281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178194342,"end":178194709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169016.16","gene_symbol":"E2F6","gene_name":"E2F transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:3120]","synonyms":"E2F-6","biotype":"protein_coding","ncbi_id":"1876","summary":"This gene encodes a member of a family of transcription factors that play a crucial role in the control of the cell cycle. The protein encoded by this gene lacks the transactivation and tumor suppressor protein association domains found in other family members, and contains a modular suppression domain that functions in the inhibition of transcription. It interacts in a complex with chromatin modifying factors. There are pseudogenes for this gene on chromosomes 22 and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":11444375,"end":11466177,"strand":-1,"description":"E2F transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:3120]"}, {"versioned_ensembl_gene_id":"ENSG00000274449.1","gene_symbol":"AC008463.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20815244,"end":20822244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282724.1","gene_symbol":"IGHD6-25","gene_name":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]","synonyms":"IGHD625","biotype":"IG_D_gene","ncbi_id":"28485","summary":null,"start":105882310,"end":105882327,"strand":-1,"description":"immunoglobulin heavy diversity 6-25 [Source:HGNC Symbol;Acc:HGNC:5516]"}, {"versioned_ensembl_gene_id":"ENSG00000271693.1","gene_symbol":"AL929325.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88369343,"end":88369459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282323.1","gene_symbol":"IGHD1-26","gene_name":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]","synonyms":"IGHD126","biotype":"IG_D_gene","ncbi_id":"28506","summary":null,"start":105881805,"end":105881824,"strand":-1,"description":"immunoglobulin heavy diversity 1-26 [Source:HGNC Symbol;Acc:HGNC:5485]"}, {"versioned_ensembl_gene_id":"ENSG00000232466.1","gene_symbol":"AL356133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26880178,"end":26880549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232899.1","gene_symbol":"CDY9P","gene_name":"chromodomain Y-linked 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:23851]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378011","summary":null,"start":18182835,"end":18184414,"strand":-1,"description":"chromodomain Y-linked 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:23851]"}, {"versioned_ensembl_gene_id":"ENSG00000260093.1","gene_symbol":"AC034111.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10050485,"end":10054254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217455.8","gene_symbol":"AC073316.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3140234,"end":3174654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157330.9","gene_symbol":"C1orf158","gene_name":"chromosome 1 open reading frame 158 [Source:HGNC Symbol;Acc:HGNC:28567]","synonyms":"MGC35194","biotype":"protein_coding","ncbi_id":"93190","summary":null,"start":12746215,"end":12763699,"strand":1,"description":"chromosome 1 open reading frame 158 [Source:HGNC Symbol;Acc:HGNC:28567]"}, {"versioned_ensembl_gene_id":"ENSG00000229465.1","gene_symbol":"ACTG1P11","gene_name":"actin gamma 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37651]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"414754","summary":null,"start":18147884,"end":18149008,"strand":1,"description":"actin gamma 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37651]"}, {"versioned_ensembl_gene_id":"ENSG00000114744.8","gene_symbol":"COMMD2","gene_name":"COMM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24993]","synonyms":"HSPC042","biotype":"protein_coding","ncbi_id":"51122","summary":null,"start":149738470,"end":149752499,"strand":-1,"description":"COMM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24993]"}, {"versioned_ensembl_gene_id":"ENSG00000244695.5","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30223542,"end":30315616,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000179443.5","gene_symbol":"OR13C6P","gene_name":"olfactory receptor family 13 subfamily C member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15101]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"392311","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":35991336,"end":35992285,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:15101]"}, {"versioned_ensembl_gene_id":"ENSG00000284650.1","gene_symbol":"AL031430.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37133489,"end":37136146,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259564.1","gene_symbol":"AC009554.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61834752,"end":61852152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259278.1","gene_symbol":"AC087878.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39019233,"end":39024918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259450.1","gene_symbol":"AC113146.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39188438,"end":39194309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228334.1","gene_symbol":"AC024028.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3083252,"end":3086421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259284.1","gene_symbol":"LINC02349","gene_name":"long intergenic non-protein coding RNA 2349 [Source:HGNC Symbol;Acc:HGNC:53271]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506530","summary":null,"start":61729850,"end":61731389,"strand":1,"description":"long intergenic non-protein coding RNA 2349 [Source:HGNC Symbol;Acc:HGNC:53271]"}, {"versioned_ensembl_gene_id":"ENSG00000154608.14","gene_symbol":"CEP170P1","gene_name":"centrosomal protein 170 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28364]","synonyms":"MGC26143,KIAA0470L,FAM68B,CEP170L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645455","summary":"This locus appears to be a transcribed pseudogene similar to centrosomal protein 170kDa (CEP170). An approximately 50 kb region upstream of this locus also is homologous to CEP170, but is not transcribed. [provided by RefSeq, Jul 2008]","start":118467590,"end":118554100,"strand":1,"description":"centrosomal protein 170 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28364]"}, {"versioned_ensembl_gene_id":"ENSG00000164125.15","gene_symbol":"FAM198B","gene_name":"family with sequence similarity 198 member B [Source:HGNC Symbol;Acc:HGNC:25312]","synonyms":"FLJ38155,ENED,DKFZp434L142,C4orf18","biotype":"protein_coding","ncbi_id":"51313","summary":null,"start":158124474,"end":158173318,"strand":-1,"description":"family with sequence similarity 198 member B [Source:HGNC Symbol;Acc:HGNC:25312]"}, {"versioned_ensembl_gene_id":"ENSG00000267051.1","gene_symbol":"AP005229.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11366913,"end":11378409,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276572.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54733008,"end":54744567,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000234728.9","gene_symbol":"C6orf48","gene_name":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]","synonyms":"G8,D6S57","biotype":"protein_coding","ncbi_id":"50854","summary":null,"start":31901630,"end":31906788,"strand":1,"description":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]"}, {"versioned_ensembl_gene_id":"ENSG00000175779.1","gene_symbol":"C15orf53","gene_name":"chromosome 15 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:33796]","synonyms":"FLJ35695","biotype":"protein_coding","ncbi_id":"400359","summary":null,"start":38696598,"end":38700038,"strand":1,"description":"chromosome 15 open reading frame 53 [Source:HGNC Symbol;Acc:HGNC:33796]"}, {"versioned_ensembl_gene_id":"ENSG00000267651.1","gene_symbol":"AC015961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37234119,"end":37236242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226577.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30414715,"end":30419319,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000064490.13","gene_symbol":"RFXANK","gene_name":"regulatory factor X associated ankyrin containing protein [Source:HGNC Symbol;Acc:HGNC:9987]","synonyms":"RFX-B,MGC138628,F14150_1,BLS,ANKRA1","biotype":"protein_coding","ncbi_id":"8625","summary":"Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013]","start":19192229,"end":19201869,"strand":1,"description":"regulatory factor X associated ankyrin containing protein [Source:HGNC Symbol;Acc:HGNC:9987]"}, {"versioned_ensembl_gene_id":"ENSG00000113851.14","gene_symbol":"CRBN","gene_name":"cereblon [Source:HGNC Symbol;Acc:HGNC:30185]","synonyms":"MRT2A,MRT2","biotype":"protein_coding","ncbi_id":"51185","summary":"This gene encodes a protein related to the Lon protease protein family. In rodents and other mammals this gene product is found in the cytoplasm localized with a calcium channel membrane protein, and is thought to play a role in brain development. Mutations in this gene are associated with autosomal recessive nonsyndromic cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":3144628,"end":3179727,"strand":-1,"description":"cereblon [Source:HGNC Symbol;Acc:HGNC:30185]"}, {"versioned_ensembl_gene_id":"ENSG00000278889.4","gene_symbol":"OR2S2","gene_name":"olfactory receptor family 2 subfamily S member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8276]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56656","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":35957108,"end":35958154,"strand":-1,"description":"olfactory receptor family 2 subfamily S member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8276]"}, {"versioned_ensembl_gene_id":"ENSG00000259845.1","gene_symbol":"HERC2P10","gene_name":"hect domain and RLD 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39056]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390561","summary":null,"start":30815271,"end":30844153,"strand":1,"description":"hect domain and RLD 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39056]"}, {"versioned_ensembl_gene_id":"ENSG00000171109.18","gene_symbol":"MFN1","gene_name":"mitofusin 1 [Source:HGNC Symbol;Acc:HGNC:18262]","synonyms":"FLJ20693","biotype":"protein_coding","ncbi_id":"55669","summary":"The protein encoded by this gene is a mediator of mitochondrial fusion. This protein and mitofusin 2 are homologs of the Drosophila protein fuzzy onion (Fzo). They are mitochondrial membrane proteins that interact with each other to facilitate mitochondrial targeting. [provided by RefSeq, Jul 2008]","start":179347692,"end":179394931,"strand":1,"description":"mitofusin 1 [Source:HGNC Symbol;Acc:HGNC:18262]"}, {"versioned_ensembl_gene_id":"ENSG00000039139.9","gene_symbol":"DNAH5","gene_name":"dynein axonemal heavy chain 5 [Source:HGNC Symbol;Acc:HGNC:2950]","synonyms":"HL1,Dnahc5,CILD3,PCD,KTGNR","biotype":"protein_coding","ncbi_id":"1767","summary":"This gene encodes a dynein protein, which is part of a microtubule-associated motor protein complex consisting of heavy, light, and intermediate chains. This protein is an axonemal heavy chain dynein. It functions as a force-generating protein with ATPase activity, whereby the release of ADP is thought to produce the force-producing power stroke. Mutations in this gene cause primary ciliary dyskinesia type 3, as well as Kartagener syndrome, which are both diseases due to ciliary defects. [provided by RefSeq, Oct 2009]","start":13690331,"end":13944543,"strand":-1,"description":"dynein axonemal heavy chain 5 [Source:HGNC Symbol;Acc:HGNC:2950]"}, {"versioned_ensembl_gene_id":"ENSG00000280140.1","gene_symbol":"AC098679.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":158111361,"end":158111931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251423.2","gene_symbol":"AC016576.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":13860303,"end":13900749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275153.4","gene_symbol":"TBC1D3K","gene_name":"TBC1 domain family member 3K [Source:HGNC Symbol;Acc:HGNC:51245]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060351","summary":null,"start":37928493,"end":37939442,"strand":1,"description":"TBC1 domain family member 3K [Source:HGNC Symbol;Acc:HGNC:51245]"}, {"versioned_ensembl_gene_id":"ENSG00000215507.10","gene_symbol":"RBMY2DP","gene_name":"RNA binding motif protein, Y-linked, family 2, member D pseudogene [Source:HGNC Symbol;Acc:HGNC:23259]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"347598","summary":null,"start":26123674,"end":26133308,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member D pseudogene [Source:HGNC Symbol;Acc:HGNC:23259]"}, {"versioned_ensembl_gene_id":"ENSG00000225174.1","gene_symbol":"OSTM1-AS1","gene_name":"OSTM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43666]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287366","summary":null,"start":108123515,"end":108159392,"strand":1,"description":"OSTM1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43666]"}, {"versioned_ensembl_gene_id":"ENSG00000162692.10","gene_symbol":"VCAM1","gene_name":"vascular cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:12663]","synonyms":"CD106","biotype":"protein_coding","ncbi_id":"7412","summary":"This gene is a member of the Ig superfamily and encodes a cell surface sialoglycoprotein expressed by cytokine-activated endothelium. This type I membrane protein mediates leukocyte-endothelial cell adhesion and signal transduction, and may play a role in the development of artherosclerosis and rheumatoid arthritis. Three alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Dec 2010]","start":100719742,"end":100739045,"strand":1,"description":"vascular cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:12663]"}, {"versioned_ensembl_gene_id":"ENSG00000229508.2","gene_symbol":"PHKG1P4","gene_name":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33918]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100151641","summary":null,"start":57060590,"end":57061301,"strand":-1,"description":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33918]"}, {"versioned_ensembl_gene_id":"ENSG00000265967.1","gene_symbol":"AC100830.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64695041,"end":64695594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282441.1","gene_symbol":"COX6CP18","gene_name":"cytochrome c oxidase subunit 6C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481684","summary":null,"start":2771356,"end":2771577,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49370]"}, {"versioned_ensembl_gene_id":"ENSG00000256812.1","gene_symbol":"CAPNS2","gene_name":"calpain small subunit 2 [Source:HGNC Symbol;Acc:HGNC:16371]","synonyms":"MGC14804,MGC12536","biotype":"protein_coding","ncbi_id":"84290","summary":null,"start":55566672,"end":55567687,"strand":1,"description":"calpain small subunit 2 [Source:HGNC Symbol;Acc:HGNC:16371]"}, {"versioned_ensembl_gene_id":"ENSG00000215271.7","gene_symbol":"HOMEZ","gene_name":"homeobox and leucine zipper encoding [Source:HGNC Symbol;Acc:HGNC:20164]","synonyms":"KIAA1443","biotype":"protein_coding","ncbi_id":"57594","summary":null,"start":23272422,"end":23299447,"strand":-1,"description":"homeobox and leucine zipper encoding [Source:HGNC Symbol;Acc:HGNC:20164]"}, {"versioned_ensembl_gene_id":"ENSG00000160752.14","gene_symbol":"FDPS","gene_name":"farnesyl diphosphate synthase [Source:HGNC Symbol;Acc:HGNC:3631]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2224","summary":"This gene encodes an enzyme that catalyzes the production of geranyl pyrophosphate and farnesyl pyrophosphate from isopentenyl pyrophosphate and dimethylallyl pyrophosphate. The resulting product, farnesyl pyrophosphate, is a key intermediate in cholesterol and sterol biosynthesis, a substrate for protein farnesylation and geranylgeranylation, and a ligand or agonist for certain hormone receptors and growth receptors. Drugs that inhibit this enzyme prevent the post-translational modifications of small GTPases and have been used to treat diseases related to bone resorption. Multiple pseudogenes have been found on chromosomes 1, 7, 14, 15, 21 and X. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2008]","start":155308748,"end":155320666,"strand":1,"description":"farnesyl diphosphate synthase [Source:HGNC Symbol;Acc:HGNC:3631]"}, {"versioned_ensembl_gene_id":"ENSG00000180574.3","gene_symbol":"AC068775.1","gene_name":"Putative eukaryotic translation initiation factor 2 subunit 3-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q2VIR3]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10505602,"end":10523135,"strand":1,"description":"Putative eukaryotic translation initiation factor 2 subunit 3-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q2VIR3]"}, {"versioned_ensembl_gene_id":"ENSG00000277290.1","gene_symbol":"AC136475.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":243099,"end":243483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231350.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":31047625,"end":31053805,"strand":1,"description":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]"}, {"versioned_ensembl_gene_id":"ENSG00000224511.1","gene_symbol":"LINC00365","gene_name":"long intergenic non-protein coding RNA 365 [Source:HGNC Symbol;Acc:HGNC:42687]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874146","summary":null,"start":30103178,"end":30108875,"strand":-1,"description":"long intergenic non-protein coding RNA 365 [Source:HGNC Symbol;Acc:HGNC:42687]"}, {"versioned_ensembl_gene_id":"ENSG00000100478.14","gene_symbol":"AP4S1","gene_name":"adaptor related protein complex 4 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:575]","synonyms":"SPG52,CLA20,AP47B","biotype":"protein_coding","ncbi_id":"11154","summary":"This gene encodes a member of the adaptor complexes small subunit protein family. These proteins are components of the heterotetrameric adaptor protein complexes, which play important roles in the secretory and endocytic pathways by mediating vesicle formation and sorting of integral membrane proteins. The encoded protein is the small subunit of adaptor protein complex-4, which is associated with both clathrin- and nonclathrin-coated vesicles. Mutations in this gene are associated with spastic quadriplegic cerebral palsy-6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 6. [provided by RefSeq, Dec 2011]","start":31025106,"end":31096450,"strand":1,"description":"adaptor related protein complex 4 sigma 1 subunit [Source:HGNC Symbol;Acc:HGNC:575]"}, {"versioned_ensembl_gene_id":"ENSG00000163633.10","gene_symbol":"C4orf36","gene_name":"chromosome 4 open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:28386]","synonyms":"MGC26744","biotype":"protein_coding","ncbi_id":"132989","summary":null,"start":86876205,"end":86936202,"strand":-1,"description":"chromosome 4 open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:28386]"}, {"versioned_ensembl_gene_id":"ENSG00000140319.10","gene_symbol":"SRP14","gene_name":"signal recognition particle 14 [Source:HGNC Symbol;Acc:HGNC:11299]","synonyms":"MGC14326,ALURBP","biotype":"protein_coding","ncbi_id":"6727","summary":null,"start":40035739,"end":40039188,"strand":-1,"description":"signal recognition particle 14 [Source:HGNC Symbol;Acc:HGNC:11299]"}, {"versioned_ensembl_gene_id":"ENSG00000276212.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54771219,"end":54784641,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000283491.1","gene_symbol":"AC017104.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":231497090,"end":231507256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124827.6","gene_symbol":"GCM2","gene_name":"glial cells missing homolog 2 [Source:HGNC Symbol;Acc:HGNC:4198]","synonyms":"GCMB,hGCMb","biotype":"protein_coding","ncbi_id":"9247","summary":"This gene is a homolog of the Drosophila glial cells missing gene, which is thought to act as a binary switch between neuronal and glial cell determination. The protein encoded by this gene contains a conserved N-terminal GCM motif that has DNA-binding activity. The protein is a transcription factor that acts as a master regulator of parathyroid development. It has been suggested that this transcription factor might mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. Mutations in this gene are associated with hypoparathyroidism. [provided by RefSeq, Jul 2008]","start":10873223,"end":10881941,"strand":-1,"description":"glial cells missing homolog 2 [Source:HGNC Symbol;Acc:HGNC:4198]"}, {"versioned_ensembl_gene_id":"ENSG00000272088.1","gene_symbol":"AL512413.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3487246,"end":3487627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187555.14","gene_symbol":"USP7","gene_name":"ubiquitin specific peptidase 7 [Source:HGNC Symbol;Acc:HGNC:12630]","synonyms":"HAUSP","biotype":"protein_coding","ncbi_id":"7874","summary":"The protein encoded by this gene belongs to the peptidase C19 family, which includes ubiquitinyl hydrolases. This protein deubiquitinates target proteins such as p53 (a tumor suppressor protein) and WASH (essential for endosomal protein recycling), and regulates their activities by counteracting the opposing ubiquitin ligase activity of proteins such as HDM2 and TRIM27, involved in the respective process. Mutations in this gene have been implicated in a neurodevelopmental disorder. [provided by RefSeq, Mar 2016]","start":8892094,"end":8964514,"strand":-1,"description":"ubiquitin specific peptidase 7 [Source:HGNC Symbol;Acc:HGNC:12630]"}, {"versioned_ensembl_gene_id":"ENSG00000261794.1","gene_symbol":"GOLGA8H","gene_name":"golgin A8 family member H [Source:HGNC Symbol;Acc:HGNC:37443]","synonyms":"GOLGA6L11","biotype":"protein_coding","ncbi_id":"728498","summary":null,"start":30604126,"end":30614561,"strand":1,"description":"golgin A8 family member H [Source:HGNC Symbol;Acc:HGNC:37443]"}, {"versioned_ensembl_gene_id":"ENSG00000229709.1","gene_symbol":"USP9YP36","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:38780]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478932","summary":null,"start":25579790,"end":25588444,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:38780]"}, {"versioned_ensembl_gene_id":"ENSG00000234620.1","gene_symbol":"PUDPP1","gene_name":"pseudouridine 5'-phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20200]","synonyms":"HDHD1P1,HDHD1BP,FAM16AY","biotype":"unprocessed_pseudogene","ncbi_id":"327658","summary":null,"start":15348662,"end":15456074,"strand":-1,"description":"pseudouridine 5'-phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20200]"}, {"versioned_ensembl_gene_id":"ENSG00000248131.5","gene_symbol":"LINC01194","gene_name":"long intergenic non-protein coding RNA 1194 [Source:HGNC Symbol;Acc:HGNC:37171]","synonyms":"TAG,CT49","biotype":"lincRNA","ncbi_id":"404663","summary":null,"start":12574857,"end":12804363,"strand":1,"description":"long intergenic non-protein coding RNA 1194 [Source:HGNC Symbol;Acc:HGNC:37171]"}, {"versioned_ensembl_gene_id":"ENSG00000185483.11","gene_symbol":"ROR1","gene_name":"receptor tyrosine kinase like orphan receptor 1 [Source:HGNC Symbol;Acc:HGNC:10256]","synonyms":"NTRKR1","biotype":"protein_coding","ncbi_id":"4919","summary":"This gene encodes a receptor tyrosine kinase-like orphan receptor that modulates neurite growth in the central nervous system. The encoded protein is a glycosylated type I membrane protein that belongs to the ROR subfamily of cell surface receptors. It is a pseudokinase that lacks catalytic activity and may interact with the non-canonical Wnt signalling pathway. This gene is highly expressed during early embryonic development but expressed at very low levels in adult tissues. Increased expression of this gene is associated with B-cell chronic lymphocytic leukaemia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2012]","start":63774022,"end":64181498,"strand":1,"description":"receptor tyrosine kinase like orphan receptor 1 [Source:HGNC Symbol;Acc:HGNC:10256]"}, {"versioned_ensembl_gene_id":"ENSG00000274425.1","gene_symbol":"AC114271.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10333436,"end":10336248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146950.12","gene_symbol":"SHROOM2","gene_name":"shroom family member 2 [Source:HGNC Symbol;Acc:HGNC:630]","synonyms":"APXL","biotype":"protein_coding","ncbi_id":"357","summary":"This gene represents the human homolog of Xenopus laevis apical protein (APX) gene, which is implicated in amiloride-sensitive sodium channel activity. It is expressed in endothelial cells and facilitates the formation of a contractile network within endothelial cells. Depletion of this gene results in an increase in endothelial sprouting, migration, and angiogenesis. This gene is highly expressed in the retina, and is a strong candidate for ocular albinism type 1 syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]","start":9786456,"end":9949443,"strand":1,"description":"shroom family member 2 [Source:HGNC Symbol;Acc:HGNC:630]"}, {"versioned_ensembl_gene_id":"ENSG00000163600.12","gene_symbol":"ICOS","gene_name":"inducible T-cell costimulator [Source:HGNC Symbol;Acc:HGNC:5351]","synonyms":"CD278,AILIM","biotype":"protein_coding","ncbi_id":"29851","summary":"The protein encoded by this gene belongs to the CD28 and CTLA-4 cell-surface receptor family. It forms homodimers and plays an important role in cell-cell signaling, immune responses, and regulation of cell proliferation. [provided by RefSeq, Jul 2008]","start":203936748,"end":203961577,"strand":1,"description":"inducible T-cell costimulator [Source:HGNC Symbol;Acc:HGNC:5351]"}, {"versioned_ensembl_gene_id":"ENSG00000248543.2","gene_symbol":"NPM1P41","gene_name":"nucleophosmin 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:45220]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422249","summary":null,"start":82010665,"end":82013095,"strand":-1,"description":"nucleophosmin 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:45220]"}, {"versioned_ensembl_gene_id":"ENSG00000257220.1","gene_symbol":"FAM213AP1","gene_name":"family with sequence similarity 213 member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52407]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420900","summary":null,"start":78130337,"end":78131004,"strand":-1,"description":"family with sequence similarity 213 member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52407]"}, {"versioned_ensembl_gene_id":"ENSG00000270154.1","gene_symbol":"AC130352.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12476462,"end":12477122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069345.11","gene_symbol":"DNAJA2","gene_name":"DnaJ heat shock protein family (Hsp40) member A2 [Source:HGNC Symbol;Acc:HGNC:14884]","synonyms":"HIRIP4,DNJ3,DNAJ,CPR3","biotype":"protein_coding","ncbi_id":"10294","summary":"The protein encoded by this gene belongs to the evolutionarily conserved DNAJ/HSP40 family of proteins, which regulate molecular chaperone activity by stimulating ATPase activity. DNAJ proteins may have up to 3 distinct domains: a conserved 70-amino acid J domain, usually at the N terminus; a glycine/phenylalanine (G/F)-rich region; and a cysteine-rich domain containing 4 motifs resembling a zinc finger domain. The product of this gene works as a cochaperone of Hsp70s in protein folding and mitochondrial protein import in vitro. [provided by RefSeq, Jul 2008]","start":46955362,"end":46973788,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A2 [Source:HGNC Symbol;Acc:HGNC:14884]"}, {"versioned_ensembl_gene_id":"ENSG00000167986.13","gene_symbol":"DDB1","gene_name":"damage specific DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2717]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1642","summary":"The protein encoded by this gene is the large subunit (p127) of the heterodimeric DNA damage-binding (DDB) complex while another protein (p48) forms the small subunit. This protein complex functions in nucleotide-excision repair and binds to DNA following UV damage. Defective activity of this complex causes the repair defect in patients with xeroderma pigmentosum complementation group E (XPE) - an autosomal recessive disorder characterized by photosensitivity and early onset of carcinomas. However, it remains for mutation analysis to demonstrate whether the defect in XPE patients is in this gene or the gene encoding the small subunit. In addition, Best vitelliform mascular dystrophy is mapped to the same region as this gene on 11q, but no sequence alternations of this gene are demonstrated in Best disease patients. The protein encoded by this gene also functions as an adaptor molecule for the cullin 4 (CUL4) ubiquitin E3 ligase complex by facilitating the binding of substrates to this complex and the ubiquitination of proteins. [provided by RefSeq, May 2012]","start":61299451,"end":61342596,"strand":-1,"description":"damage specific DNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2717]"}, {"versioned_ensembl_gene_id":"ENSG00000284724.1","gene_symbol":"AC068587.9","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12659130,"end":12659348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261566.1","gene_symbol":"AC135776.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35022851,"end":35024250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273865.2","gene_symbol":"CR854858.1","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:RefSeq peptide;Acc:NP_001289480]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":13185268,"end":13186628,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:RefSeq peptide;Acc:NP_001289480]"}, {"versioned_ensembl_gene_id":"ENSG00000118785.13","gene_symbol":"SPP1","gene_name":"secreted phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:11255]","synonyms":"OPN,ETA-1,BSPI,BNSP","biotype":"protein_coding","ncbi_id":"6696","summary":"The protein encoded by this gene is involved in the attachment of osteoclasts to the mineralized bone matrix. The encoded protein is secreted and binds hydroxyapatite with high affinity. The osteoclast vitronectin receptor is found in the cell membrane and may be involved in the binding to this protein. This protein is also a cytokine that upregulates expression of interferon-gamma and interleukin-12. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":87975650,"end":87983426,"strand":1,"description":"secreted phosphoprotein 1 [Source:HGNC Symbol;Acc:HGNC:11255]"}, {"versioned_ensembl_gene_id":"ENSG00000139505.11","gene_symbol":"MTMR6","gene_name":"myotubularin related protein 6 [Source:HGNC Symbol;Acc:HGNC:7453]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9107","summary":null,"start":25246201,"end":25288009,"strand":-1,"description":"myotubularin related protein 6 [Source:HGNC Symbol;Acc:HGNC:7453]"}, {"versioned_ensembl_gene_id":"ENSG00000259695.2","gene_symbol":"AC090164.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101580893,"end":101581556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259464.2","gene_symbol":"SNRPCP18","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49833]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289564","summary":null,"start":101562536,"end":101562974,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49833]"}, {"versioned_ensembl_gene_id":"ENSG00000233286.1","gene_symbol":"MTND3P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42150]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873239","summary":null,"start":120212935,"end":120213275,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42150]"}, {"versioned_ensembl_gene_id":"ENSG00000170323.8","gene_symbol":"FABP4","gene_name":"fatty acid binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3559]","synonyms":"aP2,A-FABP","biotype":"protein_coding","ncbi_id":"2167","summary":"FABP4 encodes the fatty acid binding protein found in adipocytes. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism. [provided by RefSeq, Jul 2008]","start":81478419,"end":81483263,"strand":-1,"description":"fatty acid binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3559]"}, {"versioned_ensembl_gene_id":"ENSG00000228168.1","gene_symbol":"HNRNPA1P21","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344697","summary":null,"start":39334979,"end":39335939,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39539]"}, {"versioned_ensembl_gene_id":"ENSG00000233652.1","gene_symbol":"CICP1","gene_name":"capicua transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360017","summary":null,"start":25388992,"end":25391811,"strand":1,"description":"capicua transcriptional repressor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23936]"}, {"versioned_ensembl_gene_id":"ENSG00000280484.1","gene_symbol":"AL732314.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":385960,"end":404559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198685.3","gene_symbol":"LINC01565","gene_name":"long intergenic non-protein coding RNA 1565 [Source:HGNC Symbol;Acc:HGNC:17099]","synonyms":"GR6,C3orf27","biotype":"lincRNA","ncbi_id":"23434","summary":null,"start":128572000,"end":128576086,"strand":-1,"description":"long intergenic non-protein coding RNA 1565 [Source:HGNC Symbol;Acc:HGNC:17099]"}, {"versioned_ensembl_gene_id":"ENSG00000170734.11","gene_symbol":"POLH","gene_name":"DNA polymerase eta [Source:HGNC Symbol;Acc:HGNC:9181]","synonyms":"RAD30A,XP-V","biotype":"protein_coding","ncbi_id":"5429","summary":"This gene encodes a member of the Y family of specialized DNA polymerases. It copies undamaged DNA with a lower fidelity than other DNA-directed polymerases. However, it accurately replicates UV-damaged DNA; when thymine dimers are present, this polymerase inserts the complementary nucleotides in the newly synthesized DNA, thereby bypassing the lesion and suppressing the mutagenic effect of UV-induced DNA damage. This polymerase is thought to be involved in hypermutation during immunoglobulin class switch recombination. Mutations in this gene result in XPV, a variant type of xeroderma pigmentosum. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":43576150,"end":43615660,"strand":1,"description":"DNA polymerase eta [Source:HGNC Symbol;Acc:HGNC:9181]"}, {"versioned_ensembl_gene_id":"ENSG00000268834.2","gene_symbol":"OR7A1P","gene_name":"olfactory receptor family 7 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8364]","synonyms":"OR7A6P,OR19-3,OLF4p,hg513","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390895","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14891737,"end":14897845,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8364]"}, {"versioned_ensembl_gene_id":"ENSG00000251128.1","gene_symbol":"WWC2-AS1","gene_name":"WWC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41041]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928734","summary":null,"start":183233628,"end":183240634,"strand":-1,"description":"WWC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41041]"}, {"versioned_ensembl_gene_id":"ENSG00000249253.1","gene_symbol":"AC093004.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130293337,"end":130293760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279115.2","gene_symbol":"AC006386.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25307729,"end":25307803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230414.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32748576,"end":32749425,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000168757.12","gene_symbol":"TSPY2","gene_name":"testis specific protein, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23924]","synonyms":"TSPYQ1","biotype":"protein_coding","ncbi_id":"64591","summary":null,"start":6246223,"end":6249019,"strand":1,"description":"testis specific protein, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23924]"}, {"versioned_ensembl_gene_id":"ENSG00000149483.11","gene_symbol":"TMEM138","gene_name":"transmembrane protein 138 [Source:HGNC Symbol;Acc:HGNC:26944]","synonyms":"JBTS16,HSPC196","biotype":"protein_coding","ncbi_id":"51524","summary":"This gene encodes a multi-pass transmembrane protein. Reduced expression of this gene in mouse fibroblasts causes short cilia and failure of ciliogenesis. Expression of this gene is tightly coordinated with expression of the neighboring gene TMEM216. Mutations in this gene are associated with the autosomal recessive neurodevelopmental disorder Joubert Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":61362001,"end":61369509,"strand":1,"description":"transmembrane protein 138 [Source:HGNC Symbol;Acc:HGNC:26944]"}, {"versioned_ensembl_gene_id":"ENSG00000267509.5","gene_symbol":"AC010511.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28065267,"end":28125430,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123405.13","gene_symbol":"NFE2","gene_name":"nuclear factor, erythroid 2 [Source:HGNC Symbol;Acc:HGNC:7780]","synonyms":"NF-E2","biotype":"protein_coding","ncbi_id":"4778","summary":null,"start":54292111,"end":54301121,"strand":-1,"description":"nuclear factor, erythroid 2 [Source:HGNC Symbol;Acc:HGNC:7780]"}, {"versioned_ensembl_gene_id":"ENSG00000225242.2","gene_symbol":"COX6B1P7","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37677]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133210","summary":null,"start":68282388,"end":68282622,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37677]"}, {"versioned_ensembl_gene_id":"ENSG00000265544.1","gene_symbol":"AA06","gene_name":"uncharacterized LOC100506677 [Source:NCBI gene;Acc:100506677]","synonyms":"AA05,AA04,AA02","biotype":"sense_intronic","ncbi_id":"100506677","summary":null,"start":33529787,"end":33533760,"strand":-1,"description":"uncharacterized LOC100506677 [Source:NCBI gene;Acc:100506677]"}, {"versioned_ensembl_gene_id":"ENSG00000263485.1","gene_symbol":"AC004147.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":34080882,"end":34082224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264598.1","gene_symbol":"AC003687.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33052107,"end":33052867,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096996.15","gene_symbol":"IL12RB1","gene_name":"interleukin 12 receptor subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:5971]","synonyms":"IL12RB,CD212","biotype":"protein_coding","ncbi_id":"3594","summary":"The protein encoded by this gene is a type I transmembrane protein that belongs to the hemopoietin receptor superfamily. This protein binds to interleukine 12 (IL12) with a low affinity, and is thought to be a part of IL12 receptor complex. This protein forms a disulfide-linked oligomer, which is required for its IL12 binding activity. The coexpression of this and IL12RB2 proteins was shown to lead to the formation of high-affinity IL12 binding sites and reconstitution of IL12 dependent signaling. Mutations in this gene impair the development of interleukin-17-producing T lymphocytes and result in increased susceptibility to mycobacterial and Salmonella infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":18058995,"end":18098944,"strand":-1,"description":"interleukin 12 receptor subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:5971]"}, {"versioned_ensembl_gene_id":"ENSG00000244300.2","gene_symbol":"GATA2-AS1","gene_name":"GATA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51108]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927167","summary":null,"start":128489212,"end":128502348,"strand":1,"description":"GATA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51108]"}, {"versioned_ensembl_gene_id":"ENSG00000119938.8","gene_symbol":"PPP1R3C","gene_name":"protein phosphatase 1 regulatory subunit 3C [Source:HGNC Symbol;Acc:HGNC:9293]","synonyms":"PTG,PPP1R5","biotype":"protein_coding","ncbi_id":"5507","summary":"This gene encodes a carbohydrate binding protein that is a subunit of the protein phosphatase 1 (PP1) complex. PP1 catalyzes reversible protein phosphorylation, which is important in a wide range of cellular activities. The encoded protein affects glycogen biosynthesis by activating glycogen synthase and limiting glycogen breakdown by reducing glycogen phosphorylase activity. DNA hypermethylation of this gene has been found in colorectal cancer patients. The encoded protein also interacts with the laforin protein, which is a protein tyrosine phosphatase implicated in Lafora disease. [provided by RefSeq, Sep 2016]","start":91628442,"end":91633054,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 3C [Source:HGNC Symbol;Acc:HGNC:9293]"}, {"versioned_ensembl_gene_id":"ENSG00000168329.13","gene_symbol":"CX3CR1","gene_name":"C-X3-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:2558]","synonyms":"V28,GPR13,CMKDR1,CMKBRL1,CCRL1","biotype":"protein_coding","ncbi_id":"1524","summary":"Fractalkine is a transmembrane protein and chemokine involved in the adhesion and migration of leukocytes. The protein encoded by this gene is a receptor for fractalkine. The encoded protein also is a coreceptor for HIV-1, and some variations in this gene lead to increased susceptibility to HIV-1 infection and rapid progression to AIDS. Four transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":39263494,"end":39281735,"strand":-1,"description":"C-X3-C motif chemokine receptor 1 [Source:HGNC Symbol;Acc:HGNC:2558]"}, {"versioned_ensembl_gene_id":"ENSG00000228586.1","gene_symbol":"AC005042.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":158685903,"end":158753775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213449.2","gene_symbol":"GAPDHP28","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:37780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441572","summary":null,"start":91666780,"end":91667782,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:37780]"}, {"versioned_ensembl_gene_id":"ENSG00000231675.1","gene_symbol":"AC005042.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158703287,"end":158703460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179348.11","gene_symbol":"GATA2","gene_name":"GATA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4171]","synonyms":"NFE1B","biotype":"protein_coding","ncbi_id":"2624","summary":"This gene encodes a member of the GATA family of zinc-finger transcription factors that are named for the consensus nucleotide sequence they bind in the promoter regions of target genes. The encoded protein plays an essential role in regulating transcription of genes involved in the development and proliferation of hematopoietic and endocrine cell lineages. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]","start":128479427,"end":128493185,"strand":-1,"description":"GATA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4171]"}, {"versioned_ensembl_gene_id":"ENSG00000218363.1","gene_symbol":"SLC25A20P1","gene_name":"solute carrier family 25 member 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1422]","synonyms":"SLC25A20P,CACTP","biotype":"processed_pseudogene","ncbi_id":"789","summary":null,"start":52246460,"end":52247362,"strand":1,"description":"solute carrier family 25 member 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1422]"}, {"versioned_ensembl_gene_id":"ENSG00000227331.1","gene_symbol":"AC005042.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":158548425,"end":158549224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233459.1","gene_symbol":"AC125238.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203634577,"end":203636016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261687.1","gene_symbol":"AC068724.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43184079,"end":43185141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206177.6","gene_symbol":"HBM","gene_name":"hemoglobin subunit mu [Source:HGNC Symbol;Acc:HGNC:4826]","synonyms":"HBK,HBAP2","biotype":"protein_coding","ncbi_id":"3042","summary":"The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. This gene has an ORF encoding a 141 aa polypeptide which is similar to the delta globins found in reptiles and birds. This locus was originally described as a pseudogene; however, it is currently thought to be a protein-coding gene. [provided by RefSeq, Jul 2008]","start":153892,"end":166768,"strand":1,"description":"hemoglobin subunit mu [Source:HGNC Symbol;Acc:HGNC:4826]"}, {"versioned_ensembl_gene_id":"ENSG00000134321.11","gene_symbol":"RSAD2","gene_name":"radical S-adenosyl methionine domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30908]","synonyms":"viperin,vig1,cig5","biotype":"protein_coding","ncbi_id":"91543","summary":"The protein encoded by this gene is an interferon-inducible antiviral protein that belongs to the S-adenosyl-L-methionine (SAM) superfamily of enzymes. The protein plays a role in cellular antiviral response and innate immune signaling. Antiviral effects result from inhibition of viral RNA replication, interference in the secretory pathway, binding to viral proteins and dysregulation of cellular lipid metabolism. The protein has been found to inhibit both DNA and RNA viruses, including influenza virus, human immunodeficiency virus (HIV-1) and Zika virus. [provided by RefSeq, Sep 2020]","start":6865806,"end":6898239,"strand":1,"description":"radical S-adenosyl methionine domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30908]"}, {"versioned_ensembl_gene_id":"ENSG00000233031.1","gene_symbol":"AC125238.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":203672175,"end":203672423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260928.2","gene_symbol":"SPCS2P1","gene_name":"signal peptidase complex subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31885]","synonyms":"SPCS2P","biotype":"processed_pseudogene","ncbi_id":"100131250","summary":null,"start":43131008,"end":43131686,"strand":1,"description":"signal peptidase complex subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31885]"}, {"versioned_ensembl_gene_id":"ENSG00000262599.5","gene_symbol":"KIAA1147","gene_name":"KIAA1147 [Source:HGNC Symbol;Acc:HGNC:29472]","synonyms":"LCHN","biotype":"protein_coding","ncbi_id":"57189","summary":null,"start":141656728,"end":141702156,"strand":-1,"description":"KIAA1147 [Source:HGNC Symbol;Acc:HGNC:29472]"}, {"versioned_ensembl_gene_id":"ENSG00000229133.1","gene_symbol":"RPS7P4","gene_name":"ribosomal protein S7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36000]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"149224","summary":null,"start":68242474,"end":68243055,"strand":-1,"description":"ribosomal protein S7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36000]"}, {"versioned_ensembl_gene_id":"ENSG00000204394.12","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31777518,"end":31795953,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000279393.1","gene_symbol":"AL139005.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":28495633,"end":28497267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137842.6","gene_symbol":"TMEM62","gene_name":"transmembrane protein 62 [Source:HGNC Symbol;Acc:HGNC:26269]","synonyms":"FLJ23375","biotype":"protein_coding","ncbi_id":"80021","summary":null,"start":43123279,"end":43185146,"strand":1,"description":"transmembrane protein 62 [Source:HGNC Symbol;Acc:HGNC:26269]"}, {"versioned_ensembl_gene_id":"ENSG00000237708.1","gene_symbol":"AL139397.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57068914,"end":57069685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228252.9","gene_symbol":"COL6A4P2","gene_name":"collagen type VI alpha 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38501]","synonyms":"COL6A4","biotype":"transcribed_unitary_pseudogene","ncbi_id":"646300","summary":"This transcribed pseudogene represents the 3' end of a presumed ortholog to a mouse gene which encodes a collagen VI alpha 4 chain protein (GeneID 68553). The predicted ORF contains multiple premature stop codons. A large chromosome break separates this pseudogene from the 5' end of the presumed ortholog (DVWA, GeneID 344875) which is located upstream at chromosome 3p24.3. [provided by RefSeq, Jun 2009]","start":130212823,"end":130273806,"strand":1,"description":"collagen type VI alpha 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38501]"}, {"versioned_ensembl_gene_id":"ENSG00000235472.1","gene_symbol":"EIF4A1P7","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"341784","summary":null,"start":28598833,"end":28600052,"strand":1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37926]"}, {"versioned_ensembl_gene_id":"ENSG00000237622.1","gene_symbol":"ELOCP18","gene_name":"elongin C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38154]","synonyms":"TCEB1P18","biotype":"processed_pseudogene","ncbi_id":"100130626","summary":null,"start":68375327,"end":68375663,"strand":-1,"description":"elongin C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38154]"}, {"versioned_ensembl_gene_id":"ENSG00000272797.1","gene_symbol":"AC092954.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":168927475,"end":168927919,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231328.1","gene_symbol":"TPT1P7","gene_name":"tumor protein, translationally-controlled 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723852","summary":null,"start":23811144,"end":23811660,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49300]"}, {"versioned_ensembl_gene_id":"ENSG00000229440.1","gene_symbol":"AL139413.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68381441,"end":68381657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132963.7","gene_symbol":"POMP","gene_name":"proteasome maturation protein [Source:HGNC Symbol;Acc:HGNC:20330]","synonyms":"UMP1,HSPC014,C13orf12","biotype":"protein_coding","ncbi_id":"51371","summary":"The protein encoded by this gene is a molecular chaperone that binds 20S preproteasome components and is essential for 20S proteasome formation. The 20S proteasome is the proteolytically active component of the 26S proteasome complex. The encoded protein is degraded before the maturation of the 20S proteasome is complete. A variant in the 5' UTR of this gene has been associated with KLICK syndrome, a rare skin disorder.[provided by RefSeq, Aug 2010]","start":28659104,"end":28678925,"strand":1,"description":"proteasome maturation protein [Source:HGNC Symbol;Acc:HGNC:20330]"}, {"versioned_ensembl_gene_id":"ENSG00000234602.7","gene_symbol":"MCIDAS","gene_name":"multiciliate differentiation and DNA synthesis associated cell cycle protein [Source:HGNC Symbol;Acc:HGNC:40050]","synonyms":"MCIN,MCI,IDAS","biotype":"protein_coding","ncbi_id":"345643","summary":"This gene encodes a member of the geminin family of proteins. The encoded nuclear protein is required for the generation of multiciliated cells in respiratory epithelium. Mutations in this gene cause a rare mucociliary clearance disorder associated with recurring respiratory infections in human patients, known as reduced generation of multiple motile cilia (RGMC). [provided by RefSeq, Sep 2016]","start":55219614,"end":55227315,"strand":-1,"description":"multiciliate differentiation and DNA synthesis associated cell cycle protein [Source:HGNC Symbol;Acc:HGNC:40050]"}, {"versioned_ensembl_gene_id":"ENSG00000273619.1","gene_symbol":"AL121832.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62386303,"end":62386970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196335.12","gene_symbol":"STK31","gene_name":"serine/threonine kinase 31 [Source:HGNC Symbol;Acc:HGNC:11407]","synonyms":"TDRD8,SgK396","biotype":"protein_coding","ncbi_id":"56164","summary":"This gene is similar to a mouse gene that encodes a putative protein kinase with a tudor domain, and shows testis-specific expression. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":23710167,"end":23832513,"strand":1,"description":"serine/threonine kinase 31 [Source:HGNC Symbol;Acc:HGNC:11407]"}, {"versioned_ensembl_gene_id":"ENSG00000232062.9","gene_symbol":"HLA-DQA1","gene_name":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]","synonyms":"HLA-DQA,CELIAC1","biotype":"protein_coding","ncbi_id":"3117","summary":"HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]","start":32730753,"end":32736617,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 1 [Source:HGNC Symbol;Acc:HGNC:4942]"}, {"versioned_ensembl_gene_id":"ENSG00000274227.1","gene_symbol":"AC073575.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112018804,"end":112019430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247498.9","gene_symbol":"GPRC5D-AS1","gene_name":"GPRC5D and HEBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53599]","synonyms":"RP11-392P7.6","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12927726,"end":12984645,"strand":1,"description":"GPRC5D and HEBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53599]"}, {"versioned_ensembl_gene_id":"ENSG00000229766.6","gene_symbol":"AL021396.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8019223,"end":8043512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130656.4","gene_symbol":"HBZ","gene_name":"hemoglobin subunit zeta [Source:HGNC Symbol;Acc:HGNC:4835]","synonyms":"HBZ1,HBZ-T1","biotype":"protein_coding","ncbi_id":"3050","summary":"Zeta-globin is an alpha-like hemoglobin. The zeta-globin polypeptide is synthesized in the yolk sac of the early embryo, while alpha-globin is produced throughout fetal and adult life. The zeta-globin gene is a member of the human alpha-globin gene cluster that includes five functional genes and two pseudogenes. The order of genes is: 5' - zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 -alpha-1 - theta1 - 3'. [provided by RefSeq, Nov 2009]","start":152687,"end":154503,"strand":1,"description":"hemoglobin subunit zeta [Source:HGNC Symbol;Acc:HGNC:4835]"}, {"versioned_ensembl_gene_id":"ENSG00000089248.6","gene_symbol":"ERP29","gene_name":"endoplasmic reticulum protein 29 [Source:HGNC Symbol;Acc:HGNC:13799]","synonyms":"PDIA9,PDI-DB,ERp31,ERp29,ERp28,C12orf8","biotype":"protein_coding","ncbi_id":"10961","summary":"This gene encodes a protein which localizes to the lumen of the endoplasmic reticulum (ER). It is a member of the protein disulfide isomerase (PDI) protein family but lacks an active thioredoxin motif, suggesting that this protein does not function as a disulfide isomerase. The canonical protein dimerizes and is thought to play a role in the processing of secretory proteins within the ER. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":112013316,"end":112023451,"strand":1,"description":"endoplasmic reticulum protein 29 [Source:HGNC Symbol;Acc:HGNC:13799]"}, {"versioned_ensembl_gene_id":"ENSG00000224745.1","gene_symbol":"AC063965.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87878692,"end":87880427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134326.11","gene_symbol":"CMPK2","gene_name":"cytidine/uridine monophosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:27015]","synonyms":"UMP-CMPK2,TYKi,NDK","biotype":"protein_coding","ncbi_id":"129607","summary":"This gene encodes one of the enzymes in the nucleotide synthesis salvage pathway that may participate in terminal differentiation of monocytic cells. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":6840570,"end":6866635,"strand":-1,"description":"cytidine/uridine monophosphate kinase 2 [Source:HGNC Symbol;Acc:HGNC:27015]"}, {"versioned_ensembl_gene_id":"ENSG00000268483.1","gene_symbol":"RPL7AP69","gene_name":"ribosomal protein L7a pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:36697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271545","summary":null,"start":57065334,"end":57066139,"strand":1,"description":"ribosomal protein L7a pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:36697]"}, {"versioned_ensembl_gene_id":"ENSG00000236376.1","gene_symbol":"AL353780.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75579669,"end":75588548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272716.1","gene_symbol":"AL121658.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32165046,"end":32165757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253591.1","gene_symbol":"AC027312.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170639158,"end":170681437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145936.8","gene_symbol":"KCNMB1","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6285]","synonyms":"hslo-beta","biotype":"protein_coding","ncbi_id":"3779","summary":"MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit and the product of this gene, the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. [provided by RefSeq, Jul 2008]","start":170374671,"end":170389677,"strand":-1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 1 [Source:HGNC Symbol;Acc:HGNC:6285]"}, {"versioned_ensembl_gene_id":"ENSG00000281954.1","gene_symbol":"AC208069.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123927107,"end":123935036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280139.1","gene_symbol":"AC010297.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":176439090,"end":176439238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263120.1","gene_symbol":"AC004584.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":56982749,"end":56985104,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204173.10","gene_symbol":"LRRC37A5P","gene_name":"leucine rich repeat containing 37 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:23369]","synonyms":"C9orf29","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"652972","summary":null,"start":111602831,"end":111631289,"strand":-1,"description":"leucine rich repeat containing 37 member A5, pseudogene [Source:HGNC Symbol;Acc:HGNC:23369]"}, {"versioned_ensembl_gene_id":"ENSG00000237679.2","gene_symbol":"VDAC1P11","gene_name":"voltage dependent anion channel 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37480]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310841","summary":null,"start":94287699,"end":94288550,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37480]"}, {"versioned_ensembl_gene_id":"ENSG00000235475.1","gene_symbol":"LINC01372","gene_name":"long intergenic non-protein coding RNA 1372 [Source:HGNC Symbol;Acc:HGNC:50623]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929736","summary":null,"start":67335976,"end":67340024,"strand":1,"description":"long intergenic non-protein coding RNA 1372 [Source:HGNC Symbol;Acc:HGNC:50623]"}, {"versioned_ensembl_gene_id":"ENSG00000173757.9","gene_symbol":"STAT5B","gene_name":"signal transducer and activator of transcription 5B [Source:HGNC Symbol;Acc:HGNC:11367]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6777","summary":"The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein mediates the signal transduction triggered by various cell ligands, such as IL2, IL4, CSF1, and different growth hormones. It has been shown to be involved in diverse biological processes, such as TCR signaling, apoptosis, adult mammary gland development, and sexual dimorphism of liver gene expression. This gene was found to fuse to retinoic acid receptor-alpha (RARA) gene in a small subset of acute promyelocytic leukemias (APLL). The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL. [provided by RefSeq, Jul 2008]","start":42199168,"end":42276707,"strand":-1,"description":"signal transducer and activator of transcription 5B [Source:HGNC Symbol;Acc:HGNC:11367]"}, {"versioned_ensembl_gene_id":"ENSG00000112041.12","gene_symbol":"TULP1","gene_name":"tubby like protein 1 [Source:HGNC Symbol;Acc:HGNC:12423]","synonyms":"TUBL1,RP14,LCA15","biotype":"protein_coding","ncbi_id":"7287","summary":"This gene encodes a member of the tubby-like gene family (TULPs). Members of this family have been identified in plants, vertebrates, and invertebrates. TULP proteins share a conserved C-terminal region of approximately 200 amino acid residues. The protein encoded by this gene is thought to play a role in the physiology of photoreceptors. Mutations in this gene are associated with recessive juvenile retinitis pigmentosa and Leber congenital amaurosis-15. [provided by RefSeq, Nov 2016]","start":35497874,"end":35512938,"strand":-1,"description":"tubby like protein 1 [Source:HGNC Symbol;Acc:HGNC:12423]"}, {"versioned_ensembl_gene_id":"ENSG00000278829.1","gene_symbol":"AC099811.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42272069,"end":42275571,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277406.1","gene_symbol":"AC243756.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":146321842,"end":146328211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271121.2","gene_symbol":"NUDT4P2","gene_name":"nudix hydrolase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"170688","summary":null,"start":146298170,"end":146298715,"strand":1,"description":"nudix hydrolase 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:18013]"}, {"versioned_ensembl_gene_id":"ENSG00000248150.1","gene_symbol":"LINC02150","gene_name":"long intergenic non-protein coding RNA 2150 [Source:HGNC Symbol;Acc:HGNC:53012]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929505","summary":null,"start":16373361,"end":16440081,"strand":-1,"description":"long intergenic non-protein coding RNA 2150 [Source:HGNC Symbol;Acc:HGNC:53012]"}, {"versioned_ensembl_gene_id":"ENSG00000248403.1","gene_symbol":"NACAP6","gene_name":"nascent polypeptide associated complex alpha subunit pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49493]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132778","summary":null,"start":16192088,"end":16192709,"strand":-1,"description":"nascent polypeptide associated complex alpha subunit pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49493]"}, {"versioned_ensembl_gene_id":"ENSG00000278342.1","gene_symbol":"AL133373.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":91554410,"end":91554503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239212.2","gene_symbol":"RPL6P7","gene_name":"ribosomal protein L6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270848","summary":null,"start":155657760,"end":155658612,"strand":1,"description":"ribosomal protein L6 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35801]"}, {"versioned_ensembl_gene_id":"ENSG00000239508.1","gene_symbol":"PLCH1-AS1","gene_name":"PLCH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41231]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874035","summary":null,"start":155449184,"end":155457753,"strand":1,"description":"PLCH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41231]"}, {"versioned_ensembl_gene_id":"ENSG00000183654.8","gene_symbol":"MARCH11","gene_name":"membrane associated ring-CH-type finger 11 [Source:HGNC Symbol;Acc:HGNC:33609]","synonyms":"MARCH-XI","biotype":"protein_coding","ncbi_id":"441061","summary":"MARCH11 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). These enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their intracellular transport. March11 appears to have a role in ubiquitin-mediated protein sorting in the trans-Golgi network (TGN)-multivesicular body (MVB) transport pathway (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010]","start":16067139,"end":16180762,"strand":-1,"description":"membrane associated ring-CH-type finger 11 [Source:HGNC Symbol;Acc:HGNC:33609]"}, {"versioned_ensembl_gene_id":"ENSG00000282453.1","gene_symbol":"IGHV2-70","gene_name":"immunoglobulin heavy variable 2-70 [Source:HGNC Symbol;Acc:HGNC:5577]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28454","summary":null,"start":106794747,"end":106795266,"strand":-1,"description":"immunoglobulin heavy variable 2-70 [Source:HGNC Symbol;Acc:HGNC:5577]"}, {"versioned_ensembl_gene_id":"ENSG00000213519.2","gene_symbol":"AC132008.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197580344,"end":197580629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163162.8","gene_symbol":"RNF149","gene_name":"ring finger protein 149 [Source:HGNC Symbol;Acc:HGNC:23137]","synonyms":"FLJ90504","biotype":"protein_coding","ncbi_id":"284996","summary":null,"start":101271219,"end":101308701,"strand":-1,"description":"ring finger protein 149 [Source:HGNC Symbol;Acc:HGNC:23137]"}, {"versioned_ensembl_gene_id":"ENSG00000260483.2","gene_symbol":"AC015720.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75022980,"end":75023256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231193.1","gene_symbol":"AL157884.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32840598,"end":32841762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223807.1","gene_symbol":"BOLA3P4","gene_name":"bolA family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51443]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480324","summary":null,"start":32926051,"end":32926450,"strand":1,"description":"bolA family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51443]"}, {"versioned_ensembl_gene_id":"ENSG00000281935.1","gene_symbol":"DNAH10","gene_name":"dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]","synonyms":"FLJ43808","biotype":"protein_coding","ncbi_id":"196385","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH10 is an inner arm dynein heavy chain (Maiti et al., 2000 [PubMed 11175280]).[supplied by OMIM, Mar 2008]","start":123826687,"end":123935766,"strand":1,"description":"dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]"}, {"versioned_ensembl_gene_id":"ENSG00000138050.14","gene_symbol":"THUMPD2","gene_name":"THUMP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:14890]","synonyms":"MGC2454,C2orf8","biotype":"protein_coding","ncbi_id":"80745","summary":null,"start":39736060,"end":39779267,"strand":-1,"description":"THUMP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:14890]"}, {"versioned_ensembl_gene_id":"ENSG00000283417.1","gene_symbol":"AC024614.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33791838,"end":33816761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279674.1","gene_symbol":"AC123769.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34000789,"end":34006772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198075.9","gene_symbol":"SULT1C4","gene_name":"sulfotransferase family 1C member 4 [Source:HGNC Symbol;Acc:HGNC:11457]","synonyms":"SULT1C2,SULT1C","biotype":"protein_coding","ncbi_id":"27233","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that belongs to the SULT1 subfamily, responsible for transferring a sulfo moiety from PAPS to phenol-containing compounds. [provided by RefSeq, Jul 2008]","start":108377911,"end":108388057,"strand":1,"description":"sulfotransferase family 1C member 4 [Source:HGNC Symbol;Acc:HGNC:11457]"}, {"versioned_ensembl_gene_id":"ENSG00000181218.5","gene_symbol":"HIST3H2A","gene_name":"histone cluster 3 H2A [Source:HGNC Symbol;Acc:HGNC:20507]","synonyms":"MGC3165","biotype":"protein_coding","ncbi_id":"92815","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":228456979,"end":228457873,"strand":-1,"description":"histone cluster 3 H2A [Source:HGNC Symbol;Acc:HGNC:20507]"}, {"versioned_ensembl_gene_id":"ENSG00000214135.8","gene_symbol":"AC132008.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":197578213,"end":197627906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277564.4","gene_symbol":"RBFOX2","gene_name":"RNA binding protein, fox-1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:9906]","synonyms":"RBM9,HRNBP2,HNRBP2,FOX-2","biotype":"protein_coding","ncbi_id":"23543","summary":"This gene is one of several human genes similar to the C. elegans gene Fox-1. This gene encodes an RNA binding protein that is thought to be a key regulator of alternative exon splicing in the nervous system and other cell types. The protein binds to a conserved UGCAUG element found downstream of many alternatively spliced exons and promotes inclusion of the alternative exon in mature transcripts. The protein also interacts with the estrogen receptor 1 transcription factor and regulates estrogen receptor 1 transcriptional activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":35744967,"end":35945128,"strand":-1,"description":"RNA binding protein, fox-1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:9906]"}, {"versioned_ensembl_gene_id":"ENSG00000280043.1","gene_symbol":"AC118282.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49229573,"end":49231284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168148.3","gene_symbol":"HIST3H3","gene_name":"histone cluster 3 H3 [Source:HGNC Symbol;Acc:HGNC:4778]","synonyms":"H3t,H3FT,H3/g,H3.4","biotype":"protein_coding","ncbi_id":"8290","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is located separately from the other H3 genes that are in the histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":228424845,"end":228425325,"strand":-1,"description":"histone cluster 3 H3 [Source:HGNC Symbol;Acc:HGNC:4778]"}, {"versioned_ensembl_gene_id":"ENSG00000280247.1","gene_symbol":"AC005578.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4246339,"end":4247358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255874.2","gene_symbol":"LINC00346","gene_name":"long intergenic non-protein coding RNA 346 [Source:HGNC Symbol;Acc:HGNC:27492]","synonyms":"NCRNA00346,C13orf29","biotype":"lincRNA","ncbi_id":"283487","summary":null,"start":110863987,"end":110870251,"strand":-1,"description":"long intergenic non-protein coding RNA 346 [Source:HGNC Symbol;Acc:HGNC:27492]"}, {"versioned_ensembl_gene_id":"ENSG00000227659.1","gene_symbol":"CLYBL-AS2","gene_name":"CLYBL antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39894]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874063","summary":null,"start":99690081,"end":99690971,"strand":-1,"description":"CLYBL antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39894]"}, {"versioned_ensembl_gene_id":"ENSG00000248506.1","gene_symbol":"AC097474.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124435750,"end":124437120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137672.12","gene_symbol":"TRPC6","gene_name":"transient receptor potential cation channel subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:12338]","synonyms":"TRP6,FSGS2","biotype":"protein_coding","ncbi_id":"7225","summary":"The protein encoded by this gene forms a receptor-activated calcium channel in the cell membrane. The channel is activated by diacylglycerol and is thought to be under the control of a phosphatidylinositol second messenger system. Activation of this channel occurs independently of protein kinase C and is not triggered by low levels of intracellular calcium. Defects in this gene are a cause of focal segmental glomerulosclerosis 2 (FSGS2). [provided by RefSeq, Mar 2009]","start":101451564,"end":101872562,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:12338]"}, {"versioned_ensembl_gene_id":"ENSG00000254506.1","gene_symbol":"AP003080.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":101584295,"end":101595156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239443.1","gene_symbol":"PABPC1P10","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37992]","synonyms":"PABPL1,D3S3192","biotype":"processed_pseudogene","ncbi_id":"285314","summary":null,"start":155309427,"end":155309807,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37992]"}, {"versioned_ensembl_gene_id":"ENSG00000242790.1","gene_symbol":"AC104831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155291188,"end":155294176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249928.2","gene_symbol":"UQCRBP3","gene_name":"ubiquinol-cytochrome c reductase binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39033]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288785","summary":null,"start":14874400,"end":14874711,"strand":-1,"description":"ubiquinol-cytochrome c reductase binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39033]"}, {"versioned_ensembl_gene_id":"ENSG00000272057.1","gene_symbol":"AC016575.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14872332,"end":14872713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168269.8","gene_symbol":"FOXI1","gene_name":"forkhead box I1 [Source:HGNC Symbol;Acc:HGNC:3815]","synonyms":"FREAC6,FKHL10","biotype":"protein_coding","ncbi_id":"2299","summary":"This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4. [provided by RefSeq, Jan 2017]","start":170105897,"end":170109725,"strand":1,"description":"forkhead box I1 [Source:HGNC Symbol;Acc:HGNC:3815]"}, {"versioned_ensembl_gene_id":"ENSG00000279090.1","gene_symbol":"AP000843.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":132403360,"end":132404060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143549.19","gene_symbol":"TPM3","gene_name":"tropomyosin 3 [Source:HGNC Symbol;Acc:HGNC:12012]","synonyms":"TRK,NEM1","biotype":"protein_coding","ncbi_id":"7170","summary":"This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":154155304,"end":154194648,"strand":-1,"description":"tropomyosin 3 [Source:HGNC Symbol;Acc:HGNC:12012]"}, {"versioned_ensembl_gene_id":"ENSG00000267224.1","gene_symbol":"AC005498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56535299,"end":56535763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265689.1","gene_symbol":"AC024614.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33688803,"end":33689174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234663.5","gene_symbol":"LINC01934","gene_name":"long intergenic non-protein coding RNA 1934 [Source:HGNC Symbol;Acc:HGNC:52757]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927156","summary":null,"start":181101932,"end":181399559,"strand":1,"description":"long intergenic non-protein coding RNA 1934 [Source:HGNC Symbol;Acc:HGNC:52757]"}, {"versioned_ensembl_gene_id":"ENSG00000265697.1","gene_symbol":"AC011824.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33534110,"end":33541339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166770.10","gene_symbol":"ZNF667-AS1","gene_name":"ZNF667 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44321]","synonyms":"MORT","biotype":"lincRNA","ncbi_id":"100128252","summary":null,"start":56477250,"end":56500666,"strand":1,"description":"ZNF667 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44321]"}, {"versioned_ensembl_gene_id":"ENSG00000231739.2","gene_symbol":"GAPDHP59","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:4152]","synonyms":"GAPDL3,GAPDHL3","biotype":"processed_pseudogene","ncbi_id":"645024","summary":null,"start":187415552,"end":187415818,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:4152]"}, {"versioned_ensembl_gene_id":"ENSG00000270814.1","gene_symbol":"TMEM261P1","gene_name":"transmembrane protein 261 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49128]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289059","summary":null,"start":25169337,"end":25169676,"strand":-1,"description":"transmembrane protein 261 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49128]"}, {"versioned_ensembl_gene_id":"ENSG00000279192.1","gene_symbol":"PWAR5","gene_name":"Prader Willi/Angelman region RNA 5 [Source:HGNC Symbol;Acc:HGNC:30090]","synonyms":"PAR5,PAR-5","biotype":"TEC","ncbi_id":"8123","summary":null,"start":24985053,"end":24988232,"strand":1,"description":"Prader Willi/Angelman region RNA 5 [Source:HGNC Symbol;Acc:HGNC:30090]"}, {"versioned_ensembl_gene_id":"ENSG00000257151.1","gene_symbol":"PWAR6","gene_name":"Prader Willi/Angelman region RNA 6 [Source:HGNC Symbol;Acc:HGNC:49129]","synonyms":"PAR-6,HBT8","biotype":"lincRNA","ncbi_id":"100506965","summary":null,"start":25031873,"end":25036490,"strand":1,"description":"Prader Willi/Angelman region RNA 6 [Source:HGNC Symbol;Acc:HGNC:49129]"}, {"versioned_ensembl_gene_id":"ENSG00000203441.2","gene_symbol":"LINC00449","gene_name":"long intergenic non-protein coding RNA 449 [Source:HGNC Symbol;Acc:HGNC:42786]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478991","summary":null,"start":99499727,"end":99501052,"strand":-1,"description":"long intergenic non-protein coding RNA 449 [Source:HGNC Symbol;Acc:HGNC:42786]"}, {"versioned_ensembl_gene_id":"ENSG00000272989.1","gene_symbol":"LINC02012","gene_name":"long intergenic non-protein coding RNA 2012 [Source:HGNC Symbol;Acc:HGNC:52847]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129516","summary":null,"start":197505262,"end":197506986,"strand":-1,"description":"long intergenic non-protein coding RNA 2012 [Source:HGNC Symbol;Acc:HGNC:52847]"}, {"versioned_ensembl_gene_id":"ENSG00000100129.17","gene_symbol":"EIF3L","gene_name":"eukaryotic translation initiation factor 3 subunit L [Source:HGNC Symbol;Acc:HGNC:18138]","synonyms":"HSPC025,HSPC021,EIF3S6IP,EIF3S11,EIF3EIP","biotype":"protein_coding","ncbi_id":"51386","summary":null,"start":37848868,"end":37889407,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit L [Source:HGNC Symbol;Acc:HGNC:18138]"}, {"versioned_ensembl_gene_id":"ENSG00000229203.1","gene_symbol":"AC103564.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131829801,"end":131832031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273173.5","gene_symbol":"SNURF","gene_name":"SNRPN upstream reading frame [Source:HGNC Symbol;Acc:HGNC:11171]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8926","summary":"This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]","start":24954986,"end":24977850,"strand":1,"description":"SNRPN upstream reading frame [Source:HGNC Symbol;Acc:HGNC:11171]"}, {"versioned_ensembl_gene_id":"ENSG00000282766.1","gene_symbol":"AC217627.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130383653,"end":130384179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257647.1","gene_symbol":"AC124312.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25027736,"end":25032047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261360.1","gene_symbol":"AC010491.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14661808,"end":14664604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248596.7","gene_symbol":"AC139491.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":176143085,"end":176185155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117266.15","gene_symbol":"CDK18","gene_name":"cyclin dependent kinase 18 [Source:HGNC Symbol;Acc:HGNC:8751]","synonyms":"PCTK3,PCTAIRE3","biotype":"protein_coding","ncbi_id":"5129","summary":null,"start":205504595,"end":205532793,"strand":1,"description":"cyclin dependent kinase 18 [Source:HGNC Symbol;Acc:HGNC:8751]"}, {"versioned_ensembl_gene_id":"ENSG00000258223.6","gene_symbol":"PRSS58","gene_name":"protease, serine 58 [Source:HGNC Symbol;Acc:HGNC:39125]","synonyms":"TRYX3","biotype":"protein_coding","ncbi_id":"136541","summary":"This gene encodes a member of the trypsin family of serine proteases. This gene and several related trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. This gene was previously described as a trypsinogen-like pseudogene, but it is now thought to be a protein-coding gene. [provided by RefSeq, Jul 2008]","start":142252143,"end":142258058,"strand":-1,"description":"protease, serine 58 [Source:HGNC Symbol;Acc:HGNC:39125]"}, {"versioned_ensembl_gene_id":"ENSG00000275019.5","gene_symbol":"LILRB3","gene_name":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]","synonyms":"LIR-3,ILT5,PIRB,HL9,PIR-B,CD85a,LIR3","biotype":"protein_coding","ncbi_id":"11025","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54217293,"end":54223789,"strand":-1,"description":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]"}, {"versioned_ensembl_gene_id":"ENSG00000233329.1","gene_symbol":"AC068287.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141208082,"end":141208376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282018.1","gene_symbol":"IGHVII-65-1","gene_name":"immunoglobulin heavy variable (II)-65-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5688]","synonyms":"IGHV(II)-65-1","biotype":"IG_V_pseudogene","ncbi_id":"28359","summary":null,"start":106696478,"end":106696725,"strand":-1,"description":"immunoglobulin heavy variable (II)-65-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5688]"}, {"versioned_ensembl_gene_id":"ENSG00000238065.1","gene_symbol":"AC010740.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140898423,"end":140899106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279476.1","gene_symbol":"AC092139.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":81517824,"end":81520617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146221.9","gene_symbol":"TCTE1","gene_name":"t-complex-associated-testis-expressed 1 [Source:HGNC Symbol;Acc:HGNC:11693]","synonyms":"MGC33600,FAP155,DRC5,D6S46","biotype":"protein_coding","ncbi_id":"202500","summary":null,"start":44278743,"end":44297688,"strand":-1,"description":"t-complex-associated-testis-expressed 1 [Source:HGNC Symbol;Acc:HGNC:11693]"}, {"versioned_ensembl_gene_id":"ENSG00000230016.1","gene_symbol":"DHFRP2","gene_name":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729816","summary":null,"start":31356825,"end":31357371,"strand":-1,"description":"dihydrofolate reductase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:2863]"}, {"versioned_ensembl_gene_id":"ENSG00000151806.13","gene_symbol":"GUF1","gene_name":"GUF1 homolog, GTPase [Source:HGNC Symbol;Acc:HGNC:25799]","synonyms":"FLJ13220","biotype":"protein_coding","ncbi_id":"60558","summary":"This gene encodes a GTPase that triggers back-translocation of the elongating ribosome during mitochondrial protein synthesis. The protein contains a highly conserved C-terminal domain not found in other GTPases that facilitates tRNA binding. The encoded protein is thought to prevent misincorporation of amino acids in stressful, suboptimal conditions. An allelic variant in this gene has been associated with early infantile epileptic encephalopathy-40. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":44678427,"end":44700926,"strand":1,"description":"GUF1 homolog, GTPase [Source:HGNC Symbol;Acc:HGNC:25799]"}, {"versioned_ensembl_gene_id":"ENSG00000282599.1","gene_symbol":"IGHD2OR15-2A","gene_name":"immunoglobulin heavy diversity 2/OR15-2A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5493]","synonyms":"IGHD2OR152A,IGHD2/OR15-2A","biotype":"IG_D_gene","ncbi_id":"28333","summary":null,"start":20008402,"end":20008432,"strand":-1,"description":"immunoglobulin heavy diversity 2/OR15-2A (non-functional) [Source:HGNC Symbol;Acc:HGNC:5493]"}, {"versioned_ensembl_gene_id":"ENSG00000227715.11","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":30021043,"end":30024386,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000274236.3","gene_symbol":"IGHV3-64","gene_name":"immunoglobulin heavy variable 3-64 [Source:HGNC Symbol;Acc:HGNC:5617]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28414","summary":null,"start":106682404,"end":106682939,"strand":-1,"description":"immunoglobulin heavy variable 3-64 [Source:HGNC Symbol;Acc:HGNC:5617]"}, {"versioned_ensembl_gene_id":"ENSG00000280365.1","gene_symbol":"AC021766.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44732575,"end":44733315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232122.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824263,"end":29825242,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000170890.13","gene_symbol":"PLA2G1B","gene_name":"phospholipase A2 group IB [Source:HGNC Symbol;Acc:HGNC:9030]","synonyms":"PPLA2,PLA2A,PLA2","biotype":"protein_coding","ncbi_id":"5319","summary":"This gene encodes a secreted member of the phospholipase A2 (PLA2) class of enzymes, which is produced by the pancreatic acinar cells. The encoded calcium-dependent enzyme catalyzes the hydrolysis of the sn-2 position of membrane glycerophospholipids to release arachidonic acid (AA) and lysophospholipids. AA is subsequently converted by downstream metabolic enzymes to several bioactive lipophilic compounds (eicosanoids), including prostaglandins (PGs) and leukotrienes (LTs). The enzyme may be involved in several physiological processes including cell contraction, cell proliferation and pathological response. [provided by RefSeq, Aug 2013]","start":120322111,"end":120327789,"strand":-1,"description":"phospholipase A2 group IB [Source:HGNC Symbol;Acc:HGNC:9030]"}, {"versioned_ensembl_gene_id":"ENSG00000197579.7","gene_symbol":"TOPORS","gene_name":"TOP1 binding arginine/serine rich protein [Source:HGNC Symbol;Acc:HGNC:21653]","synonyms":"TP53BPL,RP31,LUN","biotype":"protein_coding","ncbi_id":"10210","summary":"This gene encodes a nuclear protein which is serine and arginine rich, and contains a RING-type zinc finger domain. It is highly expressed in the testis, and functions as an ubiquitin-protein E3 ligase. Mutations in this gene are associated with retinitis pigmentosa type 31. Alternatively spliced transcript variants, encoding different isoforms, have been observed for this locus. [provided by RefSeq, Sep 2010]","start":32540544,"end":32552553,"strand":-1,"description":"TOP1 binding arginine/serine rich protein [Source:HGNC Symbol;Acc:HGNC:21653]"}, {"versioned_ensembl_gene_id":"ENSG00000229946.2","gene_symbol":"B3GNT2P1","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51316]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422469","summary":null,"start":99886740,"end":99887691,"strand":-1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51316]"}, {"versioned_ensembl_gene_id":"ENSG00000282099.1","gene_symbol":"IGHVII-62-1","gene_name":"immunoglobulin heavy variable (II)-62-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5687]","synonyms":"IGHV(II)-62-1","biotype":"IG_V_pseudogene","ncbi_id":"28360","summary":null,"start":106675232,"end":106675466,"strand":-1,"description":"immunoglobulin heavy variable (II)-62-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5687]"}, {"versioned_ensembl_gene_id":"ENSG00000270308.1","gene_symbol":"AL137843.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99656997,"end":99657381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259593.1","gene_symbol":"MTND5P40","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:51959]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075256","summary":null,"start":46341354,"end":46341599,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:51959]"}, {"versioned_ensembl_gene_id":"ENSG00000198440.9","gene_symbol":"ZNF583","gene_name":"zinc finger protein 583 [Source:HGNC Symbol;Acc:HGNC:26427]","synonyms":"FLJ31030","biotype":"protein_coding","ncbi_id":"147949","summary":null,"start":56397966,"end":56436035,"strand":1,"description":"zinc finger protein 583 [Source:HGNC Symbol;Acc:HGNC:26427]"}, {"versioned_ensembl_gene_id":"ENSG00000223794.1","gene_symbol":"COX5BP8","gene_name":"cytochrome c oxidase subunit 5B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39083]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100859925","summary":null,"start":179255733,"end":179256081,"strand":1,"description":"cytochrome c oxidase subunit 5B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39083]"}, {"versioned_ensembl_gene_id":"ENSG00000273164.1","gene_symbol":"DGCR10","gene_name":"DiGeorge syndrome critical region gene 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17864]","synonyms":"DGS-B","biotype":"sense_intronic","ncbi_id":"26222","summary":null,"start":19023056,"end":19023550,"strand":1,"description":"DiGeorge syndrome critical region gene 10 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17864]"}, {"versioned_ensembl_gene_id":"ENSG00000100116.16","gene_symbol":"GCAT","gene_name":"glycine C-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:4188]","synonyms":"KBL","biotype":"protein_coding","ncbi_id":"23464","summary":"The degradation of L-threonine to glycine consists of a two-step biochemical pathway involving the enzymes L-threonine dehydrogenase and 2-amino-3-ketobutyrate coenzyme A ligase. L-Threonine is first converted into 2-amino-3-ketobutyrate by L-threonine dehydrogenase. This gene encodes the second enzyme in this pathway, which then catalyzes the reaction between 2-amino-3-ketobutyrate and coenzyme A to form glycine and acetyl-CoA. The encoded enzyme is considered a class II pyridoxal-phosphate-dependent aminotransferase. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 14. [provided by RefSeq, Jan 2010]","start":37807905,"end":37817176,"strand":1,"description":"glycine C-acetyltransferase [Source:HGNC Symbol;Acc:HGNC:4188]"}, {"versioned_ensembl_gene_id":"ENSG00000260640.1","gene_symbol":"AP003115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97241742,"end":97242204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251169.2","gene_symbol":"LINC01843","gene_name":"long intergenic non-protein coding RNA 1843 [Source:HGNC Symbol;Acc:HGNC:52659]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927934","summary":null,"start":134506552,"end":134509229,"strand":1,"description":"long intergenic non-protein coding RNA 1843 [Source:HGNC Symbol;Acc:HGNC:52659]"}, {"versioned_ensembl_gene_id":"ENSG00000258231.5","gene_symbol":"AC020637.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58544124,"end":58813060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250992.1","gene_symbol":"AC139491.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176040744,"end":176042878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177494.5","gene_symbol":"ZBED2","gene_name":"zinc finger BED-type containing 2 [Source:HGNC Symbol;Acc:HGNC:20710]","synonyms":"MGC10796","biotype":"protein_coding","ncbi_id":"79413","summary":null,"start":111592900,"end":111595443,"strand":-1,"description":"zinc finger BED-type containing 2 [Source:HGNC Symbol;Acc:HGNC:20710]"}, {"versioned_ensembl_gene_id":"ENSG00000258397.1","gene_symbol":"BCAR1P1","gene_name":"breast cancer anti-estrogen resistance 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51325]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533717","summary":null,"start":20073699,"end":20074334,"strand":-1,"description":"breast cancer anti-estrogen resistance 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51325]"}, {"versioned_ensembl_gene_id":"ENSG00000236391.3","gene_symbol":"AC092573.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":173338219,"end":173356208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008517.16","gene_symbol":"IL32","gene_name":"interleukin 32 [Source:HGNC Symbol;Acc:HGNC:16830]","synonyms":"TAIFd,TAIFb,TAIF,NK4","biotype":"protein_coding","ncbi_id":"9235","summary":"This gene encodes a member of the cytokine family. The protein contains a tyrosine sulfation site, 3 potential N-myristoylation sites, multiple putative phosphorylation sites, and an RGD cell-attachment sequence. Expression of this protein is increased after the activation of T-cells by mitogens or the activation of NK cells by IL-2. This protein induces the production of TNFalpha from macrophage cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":3065297,"end":3082192,"strand":1,"description":"interleukin 32 [Source:HGNC Symbol;Acc:HGNC:16830]"}, {"versioned_ensembl_gene_id":"ENSG00000169085.11","gene_symbol":"C8orf46","gene_name":"chromosome 8 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:28498]","synonyms":"MGC33510","biotype":"protein_coding","ncbi_id":"254778","summary":null,"start":66460003,"end":66518524,"strand":1,"description":"chromosome 8 open reading frame 46 [Source:HGNC Symbol;Acc:HGNC:28498]"}, {"versioned_ensembl_gene_id":"ENSG00000167476.10","gene_symbol":"JSRP1","gene_name":"junctional sarcoplasmic reticulum protein 1 [Source:HGNC Symbol;Acc:HGNC:24963]","synonyms":"JP-45,FLJ32416","biotype":"protein_coding","ncbi_id":"126306","summary":"The protein encoded by this gene is involved in excitation-contraction coupling at the sarcoplasmic reticulum. The encoded protein can interact with CACNA1S, CACNB1, and calsequestrin to help regulate calcium influx and efflux in skeletal muscle. [provided by RefSeq, Jul 2012]","start":2252252,"end":2269759,"strand":-1,"description":"junctional sarcoplasmic reticulum protein 1 [Source:HGNC Symbol;Acc:HGNC:24963]"}, {"versioned_ensembl_gene_id":"ENSG00000059728.10","gene_symbol":"MXD1","gene_name":"MAX dimerization protein 1 [Source:HGNC Symbol;Acc:HGNC:6761]","synonyms":"MAD1,MAD,bHLHc58","biotype":"protein_coding","ncbi_id":"4084","summary":"This gene encodes a member of the MYC/MAX/MAD network of basic helix-loop-helix leucine zipper transcription factors. The MYC/MAX/MAD transcription factors mediate cellular proliferation, differentiation and apoptosis. The encoded protein antagonizes MYC-mediated transcriptional activation of target genes by competing for the binding partner MAX and recruiting repressor complexes containing histone deacetylases. Mutations in this gene may play a role in acute leukemia, and the encoded protein is a potential tumor suppressor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]","start":69897688,"end":69942945,"strand":1,"description":"MAX dimerization protein 1 [Source:HGNC Symbol;Acc:HGNC:6761]"}, {"versioned_ensembl_gene_id":"ENSG00000175077.5","gene_symbol":"RTP1","gene_name":"receptor transporter protein 1 [Source:HGNC Symbol;Acc:HGNC:28580]","synonyms":"Z3CXXC1,MGC35450","biotype":"protein_coding","ncbi_id":"132112","summary":null,"start":187197486,"end":187201465,"strand":1,"description":"receptor transporter protein 1 [Source:HGNC Symbol;Acc:HGNC:28580]"}, {"versioned_ensembl_gene_id":"ENSG00000225056.1","gene_symbol":"AL121894.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23655225,"end":23656390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256152.2","gene_symbol":"AC027290.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122865335,"end":122867021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249301.1","gene_symbol":"AC108120.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75910283,"end":75910576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260603.1","gene_symbol":"AC133539.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87892938,"end":87893685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251078.1","gene_symbol":"SLC25A5P9","gene_name":"solute carrier family 25 member 5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35468]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133074","summary":null,"start":75752570,"end":75753479,"strand":-1,"description":"solute carrier family 25 member 5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35468]"}, {"versioned_ensembl_gene_id":"ENSG00000254759.1","gene_symbol":"NAP1L1P1","gene_name":"nucleosome assembly protein 1 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729561","summary":null,"start":126067539,"end":126068601,"strand":1,"description":"nucleosome assembly protein 1 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38004]"}, {"versioned_ensembl_gene_id":"ENSG00000232165.1","gene_symbol":"AC006455.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63345840,"end":63346732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283399.1","gene_symbol":"AC004381.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20711473,"end":20732990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231349.2","gene_symbol":"AC119749.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86404176,"end":86404866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183722.7","gene_symbol":"LHFPL6","gene_name":"LHFPL tetraspan subfamily member 6 [Source:HGNC Symbol;Acc:HGNC:6586]","synonyms":"MGC22429,LHFP","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":39342892,"end":39603528,"strand":-1,"description":"LHFPL tetraspan subfamily member 6 [Source:HGNC Symbol;Acc:HGNC:6586]"}, {"versioned_ensembl_gene_id":"ENSG00000176009.3","gene_symbol":"ASCL3","gene_name":"achaete-scute family bHLH transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:740]","synonyms":"Sgn1,HASH3,bHLHa42","biotype":"protein_coding","ncbi_id":"56676","summary":"Basic helix-loop-helix transcription factors, such as ASCL3, are essential for the determination of cell fate and the development and differentiation of numerous tissues (Jonsson et al., 2004 [PubMed 15475265]).[supplied by OMIM, Mar 2008]","start":8937579,"end":8938211,"strand":-1,"description":"achaete-scute family bHLH transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:740]"}, {"versioned_ensembl_gene_id":"ENSG00000248240.1","gene_symbol":"AC114956.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43515274,"end":43525310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147571.4","gene_symbol":"CRH","gene_name":"corticotropin releasing hormone [Source:HGNC Symbol;Acc:HGNC:2355]","synonyms":"CRH1,CRF","biotype":"protein_coding","ncbi_id":"1392","summary":"This gene encodes a member of the corticotropin-releasing factor family. The encoded preproprotein is proteolytically processed to generate the mature neuropeptide hormone. In response to stress, this hormone is secreted by the paraventricular nucleus (PVN) of the hypothalamus, binds to corticotropin releasing hormone receptors and stimulates the release of adrenocorticotropic hormone from the pituitary gland. Marked reduction in this protein has been observed in association with Alzheimer's disease. Autosomal recessive hypothalamic corticotropin deficiency has multiple and potentially fatal metabolic consequences including hypoglycemia and hepatitis. In addition to production in the hypothalamus, this protein is also synthesized in peripheral tissues, such as T lymphocytes, and is highly expressed in the placenta. In the placenta it is a marker that determines the length of gestation and the timing of parturition and delivery. A rapid increase in circulating levels of the hormone occurs at the onset of parturition, suggesting that, in addition to its metabolic functions, this protein may act as a trigger for parturition. [provided by RefSeq, Nov 2015]","start":66176382,"end":66178725,"strand":-1,"description":"corticotropin releasing hormone [Source:HGNC Symbol;Acc:HGNC:2355]"}, {"versioned_ensembl_gene_id":"ENSG00000131127.13","gene_symbol":"ZNF141","gene_name":"zinc finger protein 141 [Source:HGNC Symbol;Acc:HGNC:12926]","synonyms":"pHZ-44,D4S90","biotype":"protein_coding","ncbi_id":"7700","summary":"The protein encoded by this gene is a zinc finger protein that may be a tumor suppressor. Defects in this gene have been associated with autosomal recessive postaxial polydactyly type A. [provided by RefSeq, Jan 2017]","start":337814,"end":384864,"strand":1,"description":"zinc finger protein 141 [Source:HGNC Symbol;Acc:HGNC:12926]"}, {"versioned_ensembl_gene_id":"ENSG00000223345.3","gene_symbol":"HIST2H2BA","gene_name":"histone cluster 2 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20560]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"337875","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 1. [provided by RefSeq, Oct 2015]","start":121108210,"end":121117257,"strand":-1,"description":"histone cluster 2 H2B family member a (pseudogene) [Source:HGNC Symbol;Acc:HGNC:20560]"}, {"versioned_ensembl_gene_id":"ENSG00000259930.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"dJ377H14.3,C6orf101,HLA-90","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797294,"end":29799302,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000234889.2","gene_symbol":"AL391666.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97975878,"end":97978641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126391.13","gene_symbol":"FRMD8","gene_name":"FERM domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25462]","synonyms":"FLJ90369,FKSG44","biotype":"protein_coding","ncbi_id":"83786","summary":null,"start":65386599,"end":65413525,"strand":1,"description":"FERM domain containing 8 [Source:HGNC Symbol;Acc:HGNC:25462]"}, {"versioned_ensembl_gene_id":"ENSG00000138641.15","gene_symbol":"HERC3","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:4876]","synonyms":"KIAA0032","biotype":"protein_coding","ncbi_id":"8916","summary":"This gene encodes a member the HERC ubiquitin ligase family. The encoded protein is located in the cytosol and binds ubiquitin via a HECT domain. Mutations in this gene have been associated with colorectal and gastric carcinomas. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]","start":88521048,"end":88708542,"strand":1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 3 [Source:HGNC Symbol;Acc:HGNC:4876]"}, {"versioned_ensembl_gene_id":"ENSG00000118046.14","gene_symbol":"STK11","gene_name":"serine/threonine kinase 11 [Source:HGNC Symbol;Acc:HGNC:11389]","synonyms":"LKB1,PJS","biotype":"protein_coding","ncbi_id":"6794","summary":"This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":1177558,"end":1228435,"strand":1,"description":"serine/threonine kinase 11 [Source:HGNC Symbol;Acc:HGNC:11389]"}, {"versioned_ensembl_gene_id":"ENSG00000281406.1","gene_symbol":"BLACAT1","gene_name":"bladder cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48597]","synonyms":"onco-lncRNA-30,LINC00912,linc-UBC1","biotype":"lincRNA","ncbi_id":"101669762","summary":null,"start":205434886,"end":205437879,"strand":-1,"description":"bladder cancer associated transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48597]"}, {"versioned_ensembl_gene_id":"ENSG00000179709.8","gene_symbol":"NLRP8","gene_name":"NLR family pyrin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:22940]","synonyms":"PAN4,NOD16,NALP8,CLR19.2","biotype":"protein_coding","ncbi_id":"126205","summary":"This gene encodes a member of the nucleotide-binding oligomerization domain/ leucine rich repeat/ pyrin domain containing (NLRP) subfamily, which belongs to the Nod-like receptor family of proteins. NLRP genes play roles in the mammalian innate immune system through inflammasome formation and activation of caspases. In addition, NLRP genes have been found to function during mammalian reproduction. Consistent with a function during human preimplantation development, this gene is expressed at high levels in oocytes with decreased levels in embryos. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":55947832,"end":55988629,"strand":1,"description":"NLR family pyrin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:22940]"}, {"versioned_ensembl_gene_id":"ENSG00000125676.19","gene_symbol":"THOC2","gene_name":"THO complex 2 [Source:HGNC Symbol;Acc:HGNC:19073]","synonyms":"MRX12,dJ506G2.1,CXorf3,THO2,MRX35","biotype":"protein_coding","ncbi_id":"57187","summary":"The TREX multiprotein complex binds specifically to spliced mRNAs to facilitate mRNA export. The protein encoded by this gene is a member of the THO complex, a subset of the TREX complex. The encoded protein interacts with the THOC1 protein.[provided by RefSeq, Jun 2010]","start":123600561,"end":123733056,"strand":-1,"description":"THO complex 2 [Source:HGNC Symbol;Acc:HGNC:19073]"}, {"versioned_ensembl_gene_id":"ENSG00000204792.2","gene_symbol":"LINC01291","gene_name":"long intergenic non-protein coding RNA 1291 [Source:HGNC Symbol;Acc:HGNC:50358]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724515","summary":null,"start":74918148,"end":74938418,"strand":1,"description":"long intergenic non-protein coding RNA 1291 [Source:HGNC Symbol;Acc:HGNC:50358]"}, {"versioned_ensembl_gene_id":"ENSG00000230836.1","gene_symbol":"LINC01293","gene_name":"long intergenic non-protein coding RNA 1293 [Source:HGNC Symbol;Acc:HGNC:50362]","synonyms":"TCONS_00002938","biotype":"lincRNA","ncbi_id":"101927861","summary":null,"start":74940258,"end":74942670,"strand":1,"description":"long intergenic non-protein coding RNA 1293 [Source:HGNC Symbol;Acc:HGNC:50362]"}, {"versioned_ensembl_gene_id":"ENSG00000239513.5","gene_symbol":"LINC01210","gene_name":"long intergenic non-protein coding RNA 1210 [Source:HGNC Symbol;Acc:HGNC:49642]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507274","summary":null,"start":137771949,"end":137780878,"strand":1,"description":"long intergenic non-protein coding RNA 1210 [Source:HGNC Symbol;Acc:HGNC:49642]"}, {"versioned_ensembl_gene_id":"ENSG00000236209.1","gene_symbol":"AC104135.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74919555,"end":74924846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112149.9","gene_symbol":"CD83","gene_name":"CD83 molecule [Source:HGNC Symbol;Acc:HGNC:1703]","synonyms":"HB15,BL11","biotype":"protein_coding","ncbi_id":"9308","summary":"The protein encoded by this gene is a single-pass type I membrane protein and member of the immunoglobulin superfamily of receptors. The encoded protein may be involved in the regulation of antigen presentation. A soluble form of this protein can bind to dendritic cells and inhibit their maturation. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":14117256,"end":14136918,"strand":1,"description":"CD83 molecule [Source:HGNC Symbol;Acc:HGNC:1703]"}, {"versioned_ensembl_gene_id":"ENSG00000226648.1","gene_symbol":"PLCG1-AS1","gene_name":"PLCG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40450]","synonyms":"TOP1-AS1","biotype":"antisense_RNA","ncbi_id":"101927117","summary":null,"start":41098329,"end":41138003,"strand":-1,"description":"PLCG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40450]"}, {"versioned_ensembl_gene_id":"ENSG00000115266.11","gene_symbol":"APC2","gene_name":"APC2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:24036]","synonyms":"APCL","biotype":"protein_coding","ncbi_id":"10297","summary":"This gene encodes a strongly conserved protein that has an N-terminal coiled-coil domain followed by an armadillo domain, five 20-amino acid repeats, and two SAMP domains. This protein promotes the assembly of a multiprotein complex that recruits and phosphorylates the Wnt effector beta-catenin and targets beta-catenin for ubiquitylation and proteasomal degradation. This protein therefore plays a role in the reduction of cytoplasmic levels of beta-catenin which in turn reduces activation of Wnt target genes that play a pivotal role in the pathogenesis of various human cancers. The protein encoded by this gene is closely related to the adenomatous polyposis coli (APC) tumor-suppressor protein and has similar tumor-suppressor effects. This gene also plays a role in actin assembly, cell-cell adhesion, and microtubule network formation through its interaction with cytoskeletal proteins. This gene has its highest expression in the central nervous system and is involved in brain development through cytoskeletal regulation in neurons. Alternative splicing produces multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]","start":1446302,"end":1473244,"strand":1,"description":"APC2, WNT signaling pathway regulator [Source:HGNC Symbol;Acc:HGNC:24036]"}, {"versioned_ensembl_gene_id":"ENSG00000249001.5","gene_symbol":"AC093895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87568035,"end":87733956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282708.1","gene_symbol":"IGHVIII-47-1","gene_name":"immunoglobulin heavy variable (III)-47-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5701]","synonyms":"IGHV(III)-47-1","biotype":"IG_V_pseudogene","ncbi_id":"28344","summary":null,"start":106555822,"end":106556152,"strand":-1,"description":"immunoglobulin heavy variable (III)-47-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5701]"}, {"versioned_ensembl_gene_id":"ENSG00000282776.1","gene_symbol":"IGHV1-45","gene_name":"immunoglobulin heavy variable 1-45 [Source:HGNC Symbol;Acc:HGNC:5553]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28466","summary":null,"start":106531677,"end":106532172,"strand":-1,"description":"immunoglobulin heavy variable 1-45 [Source:HGNC Symbol;Acc:HGNC:5553]"}, {"versioned_ensembl_gene_id":"ENSG00000171180.2","gene_symbol":"OR2M4","gene_name":"olfactory receptor family 2 subfamily M member 4 [Source:HGNC Symbol;Acc:HGNC:8270]","synonyms":"TPCR100,OST710,HTPCRX18,HSHTPCRX18","biotype":"protein_coding","ncbi_id":"26245","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248231417,"end":248244679,"strand":1,"description":"olfactory receptor family 2 subfamily M member 4 [Source:HGNC Symbol;Acc:HGNC:8270]"}, {"versioned_ensembl_gene_id":"ENSG00000187536.4","gene_symbol":"TPM3P7","gene_name":"tropomyosin 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39170]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"751599","summary":null,"start":25809925,"end":25810656,"strand":-1,"description":"tropomyosin 3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39170]"}, {"versioned_ensembl_gene_id":"ENSG00000282553.1","gene_symbol":"IGHVIV-44-1","gene_name":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]","synonyms":"IGHV(IV)-44-1","biotype":"IG_V_pseudogene","ncbi_id":"28337","summary":null,"start":106514026,"end":106514437,"strand":-1,"description":"immunoglobulin heavy variable (IV)-44-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5710]"}, {"versioned_ensembl_gene_id":"ENSG00000282802.1","gene_symbol":"IGHVIII-44","gene_name":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]","synonyms":"IGHV(III)-44","biotype":"IG_V_pseudogene","ncbi_id":"28345","summary":null,"start":106502901,"end":106503074,"strand":-1,"description":"immunoglobulin heavy variable (III)-44 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5700]"}, {"versioned_ensembl_gene_id":"ENSG00000266213.1","gene_symbol":"AC107892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78137223,"end":78140887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282189.1","gene_symbol":"AC067930.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143578358,"end":143583305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279453.1","gene_symbol":"Z99129.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":122436789,"end":122439223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223533.8","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"C6orf18,HCR","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31187361,"end":31203155,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000164751.14","gene_symbol":"PEX2","gene_name":"peroxisomal biogenesis factor 2 [Source:HGNC Symbol;Acc:HGNC:9717]","synonyms":"ZWS3,RNF72,PXMP3,PMP35,PAF-1","biotype":"protein_coding","ncbi_id":"5828","summary":"This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":76980258,"end":77001044,"strand":-1,"description":"peroxisomal biogenesis factor 2 [Source:HGNC Symbol;Acc:HGNC:9717]"}, {"versioned_ensembl_gene_id":"ENSG00000242242.5","gene_symbol":"NECTIN3-AS1","gene_name":"NECTIN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40813]","synonyms":"PVRL3-AS1","biotype":"antisense_RNA","ncbi_id":"100506555","summary":null,"start":110893708,"end":111071553,"strand":-1,"description":"NECTIN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40813]"}, {"versioned_ensembl_gene_id":"ENSG00000109832.13","gene_symbol":"DDX25","gene_name":"DEAD-box helicase 25 [Source:HGNC Symbol;Acc:HGNC:18698]","synonyms":"GRTH","biotype":"protein_coding","ncbi_id":"29118","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. The encoded protein is a gonadotropin-regulated and developmentally expressed testicular RNA helicase. It may serve to maintain testicular functions related to steroidogenesis and spermatogenesis. [provided by RefSeq, Jul 2008]","start":125903348,"end":125943702,"strand":1,"description":"DEAD-box helicase 25 [Source:HGNC Symbol;Acc:HGNC:18698]"}, {"versioned_ensembl_gene_id":"ENSG00000168038.10","gene_symbol":"ULK4","gene_name":"unc-51 like kinase 4 [Source:HGNC Symbol;Acc:HGNC:15784]","synonyms":"FAM7C1,REC01035,FLJ20574","biotype":"protein_coding","ncbi_id":"54986","summary":"This gene encodes a member of the unc-51-like serine/threonine kinase (STK) family. Members of this protein family play a role in neuronal growth and endocytosis. The encoded protein is likely involved in neurite branching, neurite elongation and neuronal migration. Genome-wide association studies (GWAS) indicate an association of variations in this gene with blood pressure and hypertension. Sequence variations in this gene may also be be associated with psychiatric disorders, including schizophrenia and bipolar disorder. Pseudogenes associated with this gene have been identified and are located on chromosome 15. [provided by RefSeq, Jul 2016]","start":41246599,"end":41962430,"strand":-1,"description":"unc-51 like kinase 4 [Source:HGNC Symbol;Acc:HGNC:15784]"}, {"versioned_ensembl_gene_id":"ENSG00000127954.12","gene_symbol":"STEAP4","gene_name":"STEAP4 metalloreductase [Source:HGNC Symbol;Acc:HGNC:21923]","synonyms":"TNFAIP9,TIARP,STAMP2,SchLAH,FLJ23153","biotype":"protein_coding","ncbi_id":"79689","summary":"The protein encoded by this gene belongs to the STEAP (six transmembrane epithelial antigen of prostate) family, and resides in the golgi apparatus. It functions as a metalloreductase that has the ability to reduce both Fe(3+) to Fe(2+) and Cu(2+) to Cu(1+), using NAD(+) as acceptor. Studies in mice and human suggest that this gene maybe involved in adipocyte development and metabolism, and may contribute to the normal biology of the prostate cell, as well as prostate cancer progression. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2011]","start":88270892,"end":88306891,"strand":-1,"description":"STEAP4 metalloreductase [Source:HGNC Symbol;Acc:HGNC:21923]"}, {"versioned_ensembl_gene_id":"ENSG00000267070.1","gene_symbol":"AC026458.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5098739,"end":5142595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245532.7","gene_symbol":"NEAT1","gene_name":"nuclear paraspeckle assembly transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30815]","synonyms":"VINC,TncRNA,NCRNA00084,MENepsilon/beta,LINC00084","biotype":"lincRNA","ncbi_id":"283131","summary":"This gene produces a long non-coding RNA (lncRNA) transcribed from the multiple endocrine neoplasia locus. This lncRNA is retained in the nucleus where it forms the core structural component of the paraspeckle sub-organelles. It may act as a transcriptional regulator for numerous genes, including some genes involved in cancer progression. [provided by RefSeq, Mar 2015]","start":65422774,"end":65445540,"strand":1,"description":"nuclear paraspeckle assembly transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30815]"}, {"versioned_ensembl_gene_id":"ENSG00000273963.1","gene_symbol":"ENPP7P14","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51387]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481720","summary":null,"start":5110793,"end":5148685,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51387]"}, {"versioned_ensembl_gene_id":"ENSG00000101439.8","gene_symbol":"CST3","gene_name":"cystatin C [Source:HGNC Symbol;Acc:HGNC:2475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1471","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes the most abundant extracellular inhibitor of cysteine proteases, which is found in high concentrations in biological fluids and is expressed in virtually all organs of the body. A mutation in this gene has been associated with amyloid angiopathy. Expression of this protein in vascular wall smooth muscle cells is severely reduced in both atherosclerotic and aneurysmal aortic lesions, establishing its role in vascular disease. In addition, this protein has been shown to have an antimicrobial function, inhibiting the replication of herpes simplex virus. Alternative splicing results in multiple transcript variants encoding a single protein. [provided by RefSeq, Nov 2014]","start":23626706,"end":23638473,"strand":-1,"description":"cystatin C [Source:HGNC Symbol;Acc:HGNC:2475]"}, {"versioned_ensembl_gene_id":"ENSG00000281493.1","gene_symbol":"IGLV3-31","gene_name":"immunoglobulin lambda variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5913]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28788","summary":null,"start":22613550,"end":22614270,"strand":1,"description":"immunoglobulin lambda variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5913]"}, {"versioned_ensembl_gene_id":"ENSG00000137474.19","gene_symbol":"MYO7A","gene_name":"myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]","synonyms":"USH1B,NSRD2,DFNB2,DFNA11","biotype":"protein_coding","ncbi_id":"4647","summary":"This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":77128264,"end":77215239,"strand":1,"description":"myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]"}, {"versioned_ensembl_gene_id":"ENSG00000181847.11","gene_symbol":"TIGIT","gene_name":"T-cell immunoreceptor with Ig and ITIM domains [Source:HGNC Symbol;Acc:HGNC:26838]","synonyms":"VSTM3,VSIG9,FLJ39873,DKFZp667A205","biotype":"protein_coding","ncbi_id":"201633","summary":"This gene encodes a member of the PVR (poliovirus receptor) family of immunoglobin proteins. The product of this gene is expressed on several classes of T cells including follicular B helper T cells (TFH). The protein has been shown to bind PVR with high affinity; this binding is thought to assist interactions between TFH and dendritic cells to regulate T cell dependent B cell responses.[provided by RefSeq, Sep 2009]","start":114276913,"end":114310288,"strand":1,"description":"T-cell immunoreceptor with Ig and ITIM domains [Source:HGNC Symbol;Acc:HGNC:26838]"}, {"versioned_ensembl_gene_id":"ENSG00000119121.21","gene_symbol":"TRPM6","gene_name":"transient receptor potential cation channel subfamily M member 6 [Source:HGNC Symbol;Acc:HGNC:17995]","synonyms":"FLJ22628,CHAK2,HSH,HOMG","biotype":"protein_coding","ncbi_id":"140803","summary":"This gene is predominantly expressed in the kidney and colon, and encodes a protein containing an ion channel domain and a protein kinase domain. It is crucial for magnesium homeostasis, and plays an essential role in epithelial magnesium transport and in the active magnesium absorption in the gut and kidney. Mutations in this gene are associated with hypomagnesemia with secondary hypocalcemia. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Apr 2010]","start":74722495,"end":74888094,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 6 [Source:HGNC Symbol;Acc:HGNC:17995]"}, {"versioned_ensembl_gene_id":"ENSG00000251621.1","gene_symbol":"AC009487.3","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":161424015,"end":161428774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269014.1","gene_symbol":"AC008622.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46826895,"end":46828440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258324.2","gene_symbol":"AL512310.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19653623,"end":19653742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249072.1","gene_symbol":"AC114801.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78008512,"end":78008688,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197614.10","gene_symbol":"MFAP5","gene_name":"microfibril associated protein 5 [Source:HGNC Symbol;Acc:HGNC:29673]","synonyms":"MP25,MAGP2","biotype":"protein_coding","ncbi_id":"8076","summary":"This gene encodes a 25-kD microfibril-associated glycoprotein which is a component of microfibrils of the extracellular matrix. The encoded protein promotes attachment of cells to microfibrils via alpha-V-beta-3 integrin. Deficiency of this gene in mice results in neutropenia. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":8637346,"end":8662888,"strand":-1,"description":"microfibril associated protein 5 [Source:HGNC Symbol;Acc:HGNC:29673]"}, {"versioned_ensembl_gene_id":"ENSG00000261170.1","gene_symbol":"AC009053.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74422120,"end":74435254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170893.3","gene_symbol":"TRH","gene_name":"thyrotropin releasing hormone [Source:HGNC Symbol;Acc:HGNC:12298]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7200","summary":"This gene encodes a member of the thyrotropin-releasing hormone family. Cleavage of the encoded proprotein releases mature thyrotropin-releasing hormone, which is a tripeptide hypothalamic regulatory hormone. The human proprotein contains six thyrotropin-releasing hormone tripeptides. Thyrotropin-releasing hormone is involved in the regulation and release of thyroid-stimulating hormone, as well as prolactin. Deficiency of this hormone has been associated with hypothalamic hypothyroidism. [provided by RefSeq, May 2013]","start":129974305,"end":129977938,"strand":1,"description":"thyrotropin releasing hormone [Source:HGNC Symbol;Acc:HGNC:12298]"}, {"versioned_ensembl_gene_id":"ENSG00000218180.2","gene_symbol":"SLC25A5P7","gene_name":"solute carrier family 25 member 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:513]","synonyms":"ANTP7","biotype":"processed_pseudogene","ncbi_id":"442255","summary":null,"start":121653795,"end":121654690,"strand":1,"description":"solute carrier family 25 member 5 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:513]"}, {"versioned_ensembl_gene_id":"ENSG00000140839.11","gene_symbol":"CLEC18B","gene_name":"C-type lectin domain family 18 member B [Source:HGNC Symbol;Acc:HGNC:33849]","synonyms":"MRCL2","biotype":"protein_coding","ncbi_id":"497190","summary":null,"start":74408270,"end":74421953,"strand":-1,"description":"C-type lectin domain family 18 member B [Source:HGNC Symbol;Acc:HGNC:33849]"}, {"versioned_ensembl_gene_id":"ENSG00000275598.1","gene_symbol":"AP000484.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63469376,"end":63470944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275709.1","gene_symbol":"AC090527.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45585757,"end":45586304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237353.6","gene_symbol":"PATE4","gene_name":"prostate and testis expressed 4 [Source:HGNC Symbol;Acc:HGNC:35427]","synonyms":"PATE-B,FLJ41047","biotype":"protein_coding","ncbi_id":"399968","summary":null,"start":125833316,"end":125840069,"strand":1,"description":"prostate and testis expressed 4 [Source:HGNC Symbol;Acc:HGNC:35427]"}, {"versioned_ensembl_gene_id":"ENSG00000196844.8","gene_symbol":"PATE2","gene_name":"prostate and testis expressed 2 [Source:HGNC Symbol;Acc:HGNC:32249]","synonyms":"UNQ3112,PATE-M,LVLF3112,C11orf38","biotype":"protein_coding","ncbi_id":"399967","summary":null,"start":125776113,"end":125778819,"strand":-1,"description":"prostate and testis expressed 2 [Source:HGNC Symbol;Acc:HGNC:32249]"}, {"versioned_ensembl_gene_id":"ENSG00000237508.10","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29719844,"end":29735599,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000264693.1","gene_symbol":"AC123786.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77622552,"end":77624515,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237623.1","gene_symbol":"AL591503.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47273366,"end":47274390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236253.7","gene_symbol":"SLC25A3P1","gene_name":"solute carrier family 25 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26869]","synonyms":"FLJ40434","biotype":"transcribed_processed_pseudogene","ncbi_id":"163742","summary":null,"start":53413149,"end":53440020,"strand":-1,"description":"solute carrier family 25 member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26869]"}, {"versioned_ensembl_gene_id":"ENSG00000214433.4","gene_symbol":"GOLGA2P8","gene_name":"golgin A2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49922]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728477","summary":null,"start":90291962,"end":90295683,"strand":1,"description":"golgin A2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49922]"}, {"versioned_ensembl_gene_id":"ENSG00000175193.13","gene_symbol":"PARL","gene_name":"presenilin associated rhomboid like [Source:HGNC Symbol;Acc:HGNC:18253]","synonyms":"RHBDS1,PSARL1,PSARL,PRO2207","biotype":"protein_coding","ncbi_id":"55486","summary":"This gene encodes a member of the rhomboid family of intramembrane serine proteases that is localized to the inner mitochondrial membrane. The encoded protein regulates mitochondrial remodeling and apoptosis through regulated substrate proteolysis. Proteolytic processing of the encoded protein results in the release of a small peptide, P-beta, which may transit to the nucleus. Mutations in this gene may be associated with Parkinson's disease. [provided by RefSeq, May 2016]","start":183829271,"end":183884933,"strand":-1,"description":"presenilin associated rhomboid like [Source:HGNC Symbol;Acc:HGNC:18253]"}, {"versioned_ensembl_gene_id":"ENSG00000102226.9","gene_symbol":"USP11","gene_name":"ubiquitin specific peptidase 11 [Source:HGNC Symbol;Acc:HGNC:12609]","synonyms":"UHX1","biotype":"protein_coding","ncbi_id":"8237","summary":"Protein ubiquitination controls many intracellular processes, including cell cycle progression, transcriptional activation, and signal transduction. This dynamic process, involving ubiquitin conjugating enzymes and deubiquitinating enzymes, adds and removes ubiquitin. Deubiquitinating enzymes are cysteine proteases that specifically cleave ubiquitin from ubiquitin-conjugated protein substrates. This gene encodes a deubiquitinating enzyme which lies in a gene cluster on chromosome Xp11.23 [provided by RefSeq, Jul 2008]","start":47232690,"end":47248328,"strand":1,"description":"ubiquitin specific peptidase 11 [Source:HGNC Symbol;Acc:HGNC:12609]"}, {"versioned_ensembl_gene_id":"ENSG00000261316.1","gene_symbol":"LINC01834","gene_name":"long intergenic non-protein coding RNA 1834 [Source:HGNC Symbol;Acc:HGNC:52648]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985280","summary":null,"start":30907199,"end":30909155,"strand":1,"description":"long intergenic non-protein coding RNA 1834 [Source:HGNC Symbol;Acc:HGNC:52648]"}, {"versioned_ensembl_gene_id":"ENSG00000111783.12","gene_symbol":"RFX4","gene_name":"regulatory factor X4 [Source:HGNC Symbol;Acc:HGNC:9985]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5992","summary":"This gene is a member of the regulatory factor X gene family, which encodes transcription factors that contain a highly-conserved winged helix DNA binding domain. The protein encoded by this gene is structurally related to regulatory factors X1, X2, X3, and X5. It has been shown to interact with itself as well as with regulatory factors X2 and X3, but it does not interact with regulatory factor X1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]","start":106582907,"end":106762803,"strand":1,"description":"regulatory factor X4 [Source:HGNC Symbol;Acc:HGNC:9985]"}, {"versioned_ensembl_gene_id":"ENSG00000184056.14","gene_symbol":"VPS33B","gene_name":"VPS33B, late endosome and lysosome associated [Source:HGNC Symbol;Acc:HGNC:12712]","synonyms":"FLJ14848","biotype":"protein_coding","ncbi_id":"26276","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec-1 domain family, and encodes the human ortholog of rat Vps33b which is homologous to the yeast class C Vps33 protein. The mammalian class C vacuolar protein sorting proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Mutations in this gene are associated with arthrogryposis-renal dysfunction-cholestasis syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":90998416,"end":91022603,"strand":-1,"description":"VPS33B, late endosome and lysosome associated [Source:HGNC Symbol;Acc:HGNC:12712]"}, {"versioned_ensembl_gene_id":"ENSG00000257711.1","gene_symbol":"AC079385.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106680758,"end":106684700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221823.10","gene_symbol":"PPP3R1","gene_name":"protein phosphatase 3 regulatory subunit B, alpha [Source:HGNC Symbol;Acc:HGNC:9317]","synonyms":"CNB1,CNB,CALNB1","biotype":"protein_coding","ncbi_id":"5534","summary":null,"start":68178857,"end":68256237,"strand":-1,"description":"protein phosphatase 3 regulatory subunit B, alpha [Source:HGNC Symbol;Acc:HGNC:9317]"}, {"versioned_ensembl_gene_id":"ENSG00000134602.15","gene_symbol":"STK26","gene_name":"serine/threonine kinase 26 [Source:HGNC Symbol;Acc:HGNC:18174]","synonyms":"MST4,MASK","biotype":"protein_coding","ncbi_id":"51765","summary":"The product of this gene is a member of the GCK group III family of kinases, which are a subset of the Ste20-like kinases. The encoded protein contains an amino-terminal kinase domain, and a carboxy-terminal regulatory domain that mediates homodimerization. The protein kinase localizes to the Golgi apparatus and is specifically activated by binding to the Golgi matrix protein GM130. It is also cleaved by caspase-3 in vitro, and may function in the apoptotic pathway. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":132023265,"end":132075943,"strand":1,"description":"serine/threonine kinase 26 [Source:HGNC Symbol;Acc:HGNC:18174]"}, {"versioned_ensembl_gene_id":"ENSG00000171695.10","gene_symbol":"LKAAEAR1","gene_name":"LKAAEAR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:33718]","synonyms":"C20orf201","biotype":"protein_coding","ncbi_id":"198437","summary":null,"start":64083380,"end":64084359,"strand":-1,"description":"LKAAEAR motif containing 1 [Source:HGNC Symbol;Acc:HGNC:33718]"}, {"versioned_ensembl_gene_id":"ENSG00000001497.16","gene_symbol":"LAS1L","gene_name":"LAS1 like, ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:25726]","synonyms":"FLJ12525","biotype":"protein_coding","ncbi_id":"81887","summary":null,"start":65512582,"end":65534775,"strand":-1,"description":"LAS1 like, ribosome biogenesis factor [Source:HGNC Symbol;Acc:HGNC:25726]"}, {"versioned_ensembl_gene_id":"ENSG00000235537.1","gene_symbol":"AC009411.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21630548,"end":21636309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197977.3","gene_symbol":"ELOVL2","gene_name":"ELOVL fatty acid elongase 2 [Source:HGNC Symbol;Acc:HGNC:14416]","synonyms":"Ssc2","biotype":"protein_coding","ncbi_id":"54898","summary":null,"start":10980759,"end":11044314,"strand":-1,"description":"ELOVL fatty acid elongase 2 [Source:HGNC Symbol;Acc:HGNC:14416]"}, {"versioned_ensembl_gene_id":"ENSG00000198452.7","gene_symbol":"OR14L1P","gene_name":"olfactory receptor family 14 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15023]","synonyms":"OR5AV1P,OR5AV1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"127617","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247617143,"end":247622372,"strand":1,"description":"olfactory receptor family 14 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15023]"}, {"versioned_ensembl_gene_id":"ENSG00000196242.8","gene_symbol":"OR2C3","gene_name":"olfactory receptor family 2 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:15005]","synonyms":"OST742,OR2C5P,OR2C4","biotype":"protein_coding","ncbi_id":"81472","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":247524677,"end":247536440,"strand":-1,"description":"olfactory receptor family 2 subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:15005]"}, {"versioned_ensembl_gene_id":"ENSG00000063244.12","gene_symbol":"U2AF2","gene_name":"U2 small nuclear RNA auxiliary factor 2 [Source:HGNC Symbol;Acc:HGNC:23156]","synonyms":"U2AF65","biotype":"protein_coding","ncbi_id":"11338","summary":"U2 auxiliary factor (U2AF), comprised of a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the U2AF large subunit which contains a sequence-specific RNA-binding region with 3 RNA recognition motifs and an Arg/Ser-rich domain necessary for splicing. The large subunit binds to the polypyrimidine tract of introns early during spliceosome assembly. Multiple transcript variants have been detected for this gene, but the full-length natures of only two have been determined to date. [provided by RefSeq, Jul 2008]","start":55654146,"end":55674715,"strand":1,"description":"U2 small nuclear RNA auxiliary factor 2 [Source:HGNC Symbol;Acc:HGNC:23156]"}, {"versioned_ensembl_gene_id":"ENSG00000223503.1","gene_symbol":"AL353807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155590601,"end":155591262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278921.2","gene_symbol":"EPB41L4A-AS2","gene_name":"EPB41L4A antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:25643]","synonyms":"FLJ11235","biotype":"lincRNA","ncbi_id":"54508","summary":null,"start":112419583,"end":112420978,"strand":1,"description":"EPB41L4A antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:25643]"}, {"versioned_ensembl_gene_id":"ENSG00000005801.16","gene_symbol":"ZNF195","gene_name":"zinc finger protein 195 [Source:HGNC Symbol;Acc:HGNC:12986]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7748","summary":"This gene encodes a protein belonging to the Krueppel C2H2-type zinc-finger protein family. These family members are transcription factors that are implicated in a variety of cellular processes. This gene is located near the centromeric border of chromosome 11p15.5, next to an imprinted domain that is associated with maternal-specific loss of heterozygosity in Wilms' tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]","start":3339261,"end":3379222,"strand":-1,"description":"zinc finger protein 195 [Source:HGNC Symbol;Acc:HGNC:12986]"}, {"versioned_ensembl_gene_id":"ENSG00000163872.15","gene_symbol":"YEATS2","gene_name":"YEATS domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25489]","synonyms":"KIAA1197,FLJ13308,FLJ12841,FLJ10201","biotype":"protein_coding","ncbi_id":"55689","summary":"Summary: The protein encoded by this gene is a scaffolding subunit of the ATAC complex, which is a complex with acetyltransferase activity on histones H3 and H4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017]","start":183697818,"end":183812625,"strand":1,"description":"YEATS domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25489]"}, {"versioned_ensembl_gene_id":"ENSG00000278087.4","gene_symbol":"NOMO3","gene_name":"NODAL modulator 3 [Source:HGNC Symbol;Acc:HGNC:25242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"408050","summary":"This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a duplicated region on the short arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum. [provided by RefSeq, Jul 2008]","start":16317633,"end":16379962,"strand":1,"description":"NODAL modulator 3 [Source:HGNC Symbol;Acc:HGNC:25242]"}, {"versioned_ensembl_gene_id":"ENSG00000276279.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54799416,"end":54812309,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000214283.4","gene_symbol":"RAD51AP1P1","gene_name":"RAD51 associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420047","summary":null,"start":136899076,"end":136900076,"strand":-1,"description":"RAD51 associated protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49646]"}, {"versioned_ensembl_gene_id":"ENSG00000258824.2","gene_symbol":"AL122035.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64422935,"end":64448557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273218.1","gene_symbol":"AC005776.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15346068,"end":15348417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281078.1","gene_symbol":"IGKV1D-8","gene_name":"immunoglobulin kappa variable 1D-8 [Source:HGNC Symbol;Acc:HGNC:5759]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28904","summary":null,"start":90220727,"end":90221384,"strand":1,"description":"immunoglobulin kappa variable 1D-8 [Source:HGNC Symbol;Acc:HGNC:5759]"}, {"versioned_ensembl_gene_id":"ENSG00000156970.12","gene_symbol":"BUB1B","gene_name":"BUB1 mitotic checkpoint serine/threonine kinase B [Source:HGNC Symbol;Acc:HGNC:1149]","synonyms":"SSK1,MAD3L,BUBR1,Bub1A","biotype":"protein_coding","ncbi_id":"701","summary":"This gene encodes a kinase involved in spindle checkpoint function. The protein has been localized to the kinetochore and plays a role in the inhibition of the anaphase-promoting complex/cyclosome (APC/C), delaying the onset of anaphase and ensuring proper chromosome segregation. Impaired spindle checkpoint function has been found in many forms of cancer. [provided by RefSeq, Jul 2008]","start":40161023,"end":40221136,"strand":1,"description":"BUB1 mitotic checkpoint serine/threonine kinase B [Source:HGNC Symbol;Acc:HGNC:1149]"}, {"versioned_ensembl_gene_id":"ENSG00000265393.1","gene_symbol":"AC084125.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144512567,"end":144513672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230203.1","gene_symbol":"Z99714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26422071,"end":26423193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167785.8","gene_symbol":"ZNF558","gene_name":"zinc finger protein 558 [Source:HGNC Symbol;Acc:HGNC:26422]","synonyms":"FLJ30932","biotype":"protein_coding","ncbi_id":"148156","summary":null,"start":8806170,"end":8832328,"strand":-1,"description":"zinc finger protein 558 [Source:HGNC Symbol;Acc:HGNC:26422]"}, {"versioned_ensembl_gene_id":"ENSG00000105672.14","gene_symbol":"ETV2","gene_name":"ETS variant 2 [Source:HGNC Symbol;Acc:HGNC:3491]","synonyms":"ER71","biotype":"protein_coding","ncbi_id":"2116","summary":null,"start":35641745,"end":35644871,"strand":1,"description":"ETS variant 2 [Source:HGNC Symbol;Acc:HGNC:3491]"}, {"versioned_ensembl_gene_id":"ENSG00000234141.1","gene_symbol":"AC006042.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7949853,"end":7950709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235834.1","gene_symbol":"Z93022.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17528435,"end":17587160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211623.2","gene_symbol":"IGKV2D-26","gene_name":"immunoglobulin kappa variable 2D-26 [Source:HGNC Symbol;Acc:HGNC:5798]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28884","summary":null,"start":89985922,"end":89986702,"strand":1,"description":"immunoglobulin kappa variable 2D-26 [Source:HGNC Symbol;Acc:HGNC:5798]"}, {"versioned_ensembl_gene_id":"ENSG00000198818.9","gene_symbol":"SFT2D1","gene_name":"SFT2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21102]","synonyms":"pRGR1,MGC19825,C6orf83","biotype":"protein_coding","ncbi_id":"113402","summary":null,"start":166319728,"end":166342591,"strand":-1,"description":"SFT2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21102]"}, {"versioned_ensembl_gene_id":"ENSG00000275037.5","gene_symbol":"KIR3DS1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]","synonyms":"nkat10,nkat10","biotype":"protein_coding","ncbi_id":"3813","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54860882,"end":54875495,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6340]"}, {"versioned_ensembl_gene_id":"ENSG00000230313.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"antisense_RNA","ncbi_id":"414768","summary":null,"start":33144783,"end":33147767,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000213930.11","gene_symbol":"GALT","gene_name":"galactose-1-phosphate uridylyltransferase [Source:HGNC Symbol;Acc:HGNC:4135]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2592","summary":"Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":34638133,"end":34651035,"strand":1,"description":"galactose-1-phosphate uridylyltransferase [Source:HGNC Symbol;Acc:HGNC:4135]"}, {"versioned_ensembl_gene_id":"ENSG00000249368.1","gene_symbol":"AC103851.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15325296,"end":15325569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221879.3","gene_symbol":"MRPS21P3","gene_name":"mitochondrial ribosomal protein S21 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29750]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359767","summary":null,"start":197363817,"end":197364078,"strand":1,"description":"mitochondrial ribosomal protein S21 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29750]"}, {"versioned_ensembl_gene_id":"ENSG00000278691.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54830903,"end":54842719,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000225328.1","gene_symbol":"LINC01594","gene_name":"long intergenic non-protein coding RNA 1594 [Source:HGNC Symbol;Acc:HGNC:51584]","synonyms":"TCONS_l2_00015893","biotype":"antisense_RNA","ncbi_id":"102724774","summary":null,"start":108167748,"end":108217841,"strand":-1,"description":"long intergenic non-protein coding RNA 1594 [Source:HGNC Symbol;Acc:HGNC:51584]"}, {"versioned_ensembl_gene_id":"ENSG00000160870.12","gene_symbol":"CYP3A7","gene_name":"cytochrome P450 family 3 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:2640]","synonyms":"P450-HFLA,CP37","biotype":"protein_coding","ncbi_id":"1551","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes, which participate in drug metabolism and the synthesis of cholesterol, steroids and other lipids. This enzyme hydroxylates testosterone and dehydroepiandrosterone 3-sulphate, which is involved in the formation of estriol during pregnancy. This gene is part of a cluster of related genes on chromosome 7q21.1. Naturally-occurring readthrough transcription occurs between this gene and the downstream CYP3A51P pseudogene and is represented by GeneID:100861540. [provided by RefSeq, Jan 2015]","start":99705037,"end":99735196,"strand":-1,"description":"cytochrome P450 family 3 subfamily A member 7 [Source:HGNC Symbol;Acc:HGNC:2640]"}, {"versioned_ensembl_gene_id":"ENSG00000272910.1","gene_symbol":"AC090425.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179583262,"end":179583762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143797.11","gene_symbol":"MBOAT2","gene_name":"membrane bound O-acyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25193]","synonyms":"OACT2,FLJ90298,FLJ14415","biotype":"protein_coding","ncbi_id":"129642","summary":null,"start":8852690,"end":9003813,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25193]"}, {"versioned_ensembl_gene_id":"ENSG00000230539.1","gene_symbol":"AOAH-IT1","gene_name":"AOAH intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41307]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874264","summary":null,"start":36597834,"end":36600120,"strand":-1,"description":"AOAH intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41307]"}, {"versioned_ensembl_gene_id":"ENSG00000136522.13","gene_symbol":"MRPL47","gene_name":"mitochondrial ribosomal protein L47 [Source:HGNC Symbol;Acc:HGNC:16652]","synonyms":"NCM1,CGI-204","biotype":"protein_coding","ncbi_id":"57129","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. This gene is immediately adjacent to the gene for BAF complex 53 kDa subunit protein a (BAF53a), in a tail-to-tail orientation. Two transcript variants encoding different protein isoforms have been identified. [provided by RefSeq, Jul 2008]","start":179588285,"end":179604654,"strand":-1,"description":"mitochondrial ribosomal protein L47 [Source:HGNC Symbol;Acc:HGNC:16652]"}, {"versioned_ensembl_gene_id":"ENSG00000228688.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"cD0826Q1.1,COL11A2P","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33103794,"end":33107330,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000270174.1","gene_symbol":"AL022097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5664985,"end":5695272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265808.3","gene_symbol":"SEC22B","gene_name":"SEC22 homolog B, vesicle trafficking protein (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:10700]","synonyms":"sec22b,ERS-24,SEC22L1","biotype":"protein_coding","ncbi_id":"9554","summary":"The protein encoded by this gene is a member of the SEC22 family of vesicle trafficking proteins. It seems to complex with SNARE and it is thought to play a role in the ER-Golgi protein trafficking. This protein has strong similarity to Mus musculus and Cricetulus griseus proteins.[provided by RefSeq, Sep 2009]","start":120150898,"end":120176515,"strand":-1,"description":"SEC22 homolog B, vesicle trafficking protein (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:10700]"}, {"versioned_ensembl_gene_id":"ENSG00000281690.2","gene_symbol":"ADAMTS12","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 12 [Source:HGNC Symbol;Acc:HGNC:14605]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81792","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS-1) motif. Individual members of this family differ in the number of C-terminal TS-1 motifs, and some have unique C-terminal domains. The enzyme encoded by this gene contains eight TS-1 motifs. It may play roles in pulmonary cells during fetal development or in tumor processes through its proteolytic activity or as a molecule potentially involved in regulation of cell adhesion. [provided by RefSeq, Jul 2008]","start":33842143,"end":33894178,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 12 [Source:HGNC Symbol;Acc:HGNC:14605]"}, {"versioned_ensembl_gene_id":"ENSG00000262418.5","gene_symbol":"PTPRC","gene_name":"protein tyrosine phosphatase, receptor type C [Source:HGNC Symbol;Acc:HGNC:9666]","synonyms":"T200,LCA,GP180,CD45","biotype":"protein_coding","ncbi_id":"5788","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitosis, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus is classified as a receptor type PTP. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling. Alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jun 2012]","start":198650158,"end":198733963,"strand":1,"description":"protein tyrosine phosphatase, receptor type C [Source:HGNC Symbol;Acc:HGNC:9666]"}, {"versioned_ensembl_gene_id":"ENSG00000278718.3","gene_symbol":"GSDMD","gene_name":"gasdermin D [Source:HGNC Symbol;Acc:HGNC:25697]","synonyms":"GSDMDC1,FLJ12150,DF5L","biotype":"protein_coding","ncbi_id":"79792","summary":"Gasdermin D is a member of the gasdermin family. Members of this family appear to play a role in regulation of epithelial proliferation. Gasdermin D has been suggested to act as a tumor suppressor. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009]","start":143553207,"end":143563062,"strand":1,"description":"gasdermin D [Source:HGNC Symbol;Acc:HGNC:25697]"}, {"versioned_ensembl_gene_id":"ENSG00000230790.2","gene_symbol":"AC012456.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11740997,"end":11745301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136518.16","gene_symbol":"ACTL6A","gene_name":"actin like 6A [Source:HGNC Symbol;Acc:HGNC:24124]","synonyms":"INO80K,BAF53A,Arp4,Actl6","biotype":"protein_coding","ncbi_id":"86","summary":"This gene encodes a family member of actin-related proteins (ARPs), which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene encodes a 53 kDa subunit protein of the BAF (BRG1/brm-associated factor) complex in mammals, which is functionally related to SWI/SNF complex in S. cerevisiae and Drosophila; the latter is thought to facilitate transcriptional activation of specific genes by antagonizing chromatin-mediated transcriptional repression. Together with beta-actin, it is required for maximal ATPase activity of BRG1, and for the association of the BAF complex with chromatin/matrix. Three transcript variants that encode two different protein isoforms have been described. [provided by RefSeq, Jul 2008]","start":179562880,"end":179588408,"strand":1,"description":"actin like 6A [Source:HGNC Symbol;Acc:HGNC:24124]"}, {"versioned_ensembl_gene_id":"ENSG00000100266.18","gene_symbol":"PACSIN2","gene_name":"protein kinase C and casein kinase substrate in neurons 2 [Source:HGNC Symbol;Acc:HGNC:8571]","synonyms":"SDPII","biotype":"protein_coding","ncbi_id":"11252","summary":"This gene is a member of the protein kinase C and casein kinase substrate in neurons family. The encoded protein is involved in linking the actin cytoskeleton with vesicle formation by regulating tubulin polymerization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":42835412,"end":43015145,"strand":-1,"description":"protein kinase C and casein kinase substrate in neurons 2 [Source:HGNC Symbol;Acc:HGNC:8571]"}, {"versioned_ensembl_gene_id":"ENSG00000244292.1","gene_symbol":"OR9N1P","gene_name":"olfactory receptor family 9 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15096]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81383","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":141911217,"end":141911943,"strand":1,"description":"olfactory receptor family 9 subfamily N member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15096]"}, {"versioned_ensembl_gene_id":"ENSG00000230859.1","gene_symbol":"YRDCP3","gene_name":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861429","summary":null,"start":40863994,"end":40864473,"strand":1,"description":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39921]"}, {"versioned_ensembl_gene_id":"ENSG00000111341.9","gene_symbol":"MGP","gene_name":"matrix Gla protein [Source:HGNC Symbol;Acc:HGNC:7060]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4256","summary":"This gene encodes a member of the osteocalcin/matrix Gla family of proteins. The encoded vitamin K-dependent protein is secreted by chondrocytes and vascular smooth muscle cells, and functions as a physiological inhibitor of ectopic tissue calcification. Carboxylation status of the encoded protein is associated with calcification of the vasculature in human patients with cardiovascular disease and calcification of the synovial membranes in osteoarthritis patients. Mutations in this gene cause Keutel syndrome in human patients, which is characterized by abnormal cartilage calcification, peripheral pulmonary stenosis and facial hypoplasia. [provided by RefSeq, Sep 2016]","start":14881181,"end":14885926,"strand":-1,"description":"matrix Gla protein [Source:HGNC Symbol;Acc:HGNC:7060]"}, {"versioned_ensembl_gene_id":"ENSG00000275256.1","gene_symbol":"AC104307.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41189041,"end":41189236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269172.1","gene_symbol":"AC011443.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39134882,"end":39136463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060566.13","gene_symbol":"CREB3L3","gene_name":"cAMP responsive element binding protein 3 like 3 [Source:HGNC Symbol;Acc:HGNC:18855]","synonyms":"CREB-H","biotype":"protein_coding","ncbi_id":"84699","summary":"This gene encodes a member of the basic-leucine zipper family and the AMP-dependent transcription factor family. The encoded protein is localized to the endoplasmic reticulum and acts as a transcription factor activated by cyclic AMP stimulation. The encoded protein binds the cyclic AMP response element (CRE) and the box-B element and has been linked to acute inflammatory response, hepatocellular carcinoma, triglyceride metabolism, and hepcidin expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":4153601,"end":4173054,"strand":1,"description":"cAMP responsive element binding protein 3 like 3 [Source:HGNC Symbol;Acc:HGNC:18855]"}, {"versioned_ensembl_gene_id":"ENSG00000225224.1","gene_symbol":"RPS27AP12","gene_name":"ribosomal protein S27a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130446","summary":null,"start":157192368,"end":157192832,"strand":1,"description":"ribosomal protein S27a pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35732]"}, {"versioned_ensembl_gene_id":"ENSG00000278327.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2,nkat2a,nkat2b,p58,CD158B2,cl-6","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738499,"end":54753027,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000258265.1","gene_symbol":"AL929601.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18944199,"end":18945139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224051.6","gene_symbol":"CPTP","gene_name":"ceramide-1-phosphate transfer protein [Source:HGNC Symbol;Acc:HGNC:28116]","synonyms":"MGC10334,GLTPD1","biotype":"protein_coding","ncbi_id":"80772","summary":null,"start":1324756,"end":1328897,"strand":1,"description":"ceramide-1-phosphate transfer protein [Source:HGNC Symbol;Acc:HGNC:28116]"}, {"versioned_ensembl_gene_id":"ENSG00000139182.13","gene_symbol":"CLSTN3","gene_name":"calsyntenin 3 [Source:HGNC Symbol;Acc:HGNC:18371]","synonyms":"KIAA0726,CSTN3,CDHR14","biotype":"protein_coding","ncbi_id":"9746","summary":null,"start":7129698,"end":7158945,"strand":1,"description":"calsyntenin 3 [Source:HGNC Symbol;Acc:HGNC:18371]"}, {"versioned_ensembl_gene_id":"ENSG00000116731.22","gene_symbol":"PRDM2","gene_name":"PR/SET domain 2 [Source:HGNC Symbol;Acc:HGNC:9347]","synonyms":"RIZ2,RIZ1,RIZ,MTB-ZF,KMT8A,KMT8,HUMHOXY1","biotype":"protein_coding","ncbi_id":"7799","summary":"This tumor suppressor gene is a member of a nuclear histone/protein methyltransferase superfamily. It encodes a zinc finger protein that can bind to retinoblastoma protein, estrogen receptor, and the TPA-responsive element (MTE) of the heme-oxygenase-1 gene. Although the functions of this protein have not been fully characterized, it may (1) play a role in transcriptional regulation during neuronal differentiation and pathogenesis of retinoblastoma, (2) act as a transcriptional activator of the heme-oxygenase-1 gene, and (3) be a specific effector of estrogen action. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":13700198,"end":13825079,"strand":1,"description":"PR/SET domain 2 [Source:HGNC Symbol;Acc:HGNC:9347]"}, {"versioned_ensembl_gene_id":"ENSG00000073754.5","gene_symbol":"CD5L","gene_name":"CD5 molecule like [Source:HGNC Symbol;Acc:HGNC:1690]","synonyms":"Spalpha,API6","biotype":"protein_coding","ncbi_id":"922","summary":null,"start":157830914,"end":157898256,"strand":-1,"description":"CD5 molecule like [Source:HGNC Symbol;Acc:HGNC:1690]"}, {"versioned_ensembl_gene_id":"ENSG00000227151.4","gene_symbol":"PRR20D","gene_name":"proline rich 20D [Source:HGNC Symbol;Acc:HGNC:37222]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729246","summary":"This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008]","start":57160632,"end":57163653,"strand":1,"description":"proline rich 20D [Source:HGNC Symbol;Acc:HGNC:37222]"}, {"versioned_ensembl_gene_id":"ENSG00000284657.1","gene_symbol":"AL031432.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25239494,"end":25240253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214988.4","gene_symbol":"RPL7AP26","gene_name":"ribosomal protein L7a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36815]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728128","summary":null,"start":82490823,"end":82491635,"strand":-1,"description":"ribosomal protein L7a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:36815]"}, {"versioned_ensembl_gene_id":"ENSG00000233433.1","gene_symbol":"AC006144.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121024964,"end":121026563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236197.3","gene_symbol":"AC002429.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":95035731,"end":95214332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278689.1","gene_symbol":"OR2T6","gene_name":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]","synonyms":"OR2T9,OR2T6P,OST703","biotype":"protein_coding","ncbi_id":"254879","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248387950,"end":248388876,"strand":1,"description":"olfactory receptor family 2 subfamily T member 6 [Source:HGNC Symbol;Acc:HGNC:15018]"}, {"versioned_ensembl_gene_id":"ENSG00000267570.1","gene_symbol":"STK25P1","gene_name":"serine/threonine kinase 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533662","summary":null,"start":12911186,"end":12912023,"strand":1,"description":"serine/threonine kinase 25 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50361]"}, {"versioned_ensembl_gene_id":"ENSG00000181625.17","gene_symbol":"SLX1B","gene_name":"SLX1 homolog B, structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:28748]","synonyms":"MGC5178,GIYD2","biotype":"protein_coding","ncbi_id":"79008","summary":"This gene encodes a protein that is an important regulator of genome stability. The protein represents the catalytic subunit of the SLX1-SLX4 structure-specific endonuclease, which can resolve DNA secondary structures that are formed during repair and recombination processes. Two identical copies of this gene are located on the p arm of chromosome 16 due to a segmental duplication; this record represents the more telomeric copy. Alternative splicing results in multiple transcript variants. Read-through transcription also occurs between this gene and the downstream SULT1A4 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 4) gene. [provided by RefSeq, Nov 2010]","start":29454501,"end":29458219,"strand":1,"description":"SLX1 homolog B, structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:28748]"}, {"versioned_ensembl_gene_id":"ENSG00000229608.1","gene_symbol":"GOLGA2P4","gene_name":"golgin A2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38600]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873742","summary":null,"start":42784462,"end":42787100,"strand":1,"description":"golgin A2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38600]"}, {"versioned_ensembl_gene_id":"ENSG00000279853.1","gene_symbol":"AC004453.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44367140,"end":44369292,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198911.11","gene_symbol":"SREBF2","gene_name":"sterol regulatory element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11290]","synonyms":"SREBP2,bHLHd2","biotype":"protein_coding","ncbi_id":"6721","summary":"This gene encodes a member of the a ubiquitously expressed transcription factor that controls cholesterol homeostasis by regulating transcription of sterol-regulated genes. The encoded protein contains a basic helix-loop-helix-leucine zipper (bHLH-Zip) domain and binds the sterol regulatory element 1 motif. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":41833079,"end":41907308,"strand":1,"description":"sterol regulatory element binding transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:11290]"}, {"versioned_ensembl_gene_id":"ENSG00000225253.1","gene_symbol":"AC011225.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41819053,"end":41819421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267652.1","gene_symbol":"AC011712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41789162,"end":41789395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175354.18","gene_symbol":"PTPN2","gene_name":"protein tyrosine phosphatase, non-receptor type 2 [Source:HGNC Symbol;Acc:HGNC:9650]","synonyms":"TCPTP,TCELLPTP,TC-PTP,PTPT","biotype":"protein_coding","ncbi_id":"5771","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. Epidermal growth factor receptor and the adaptor protein Shc were reported to be substrates of this PTP, which suggested the roles in growth factor mediated cell signaling. Multiple alternatively spliced transcript variants encoding different isoforms have been found. Two highly related but distinctly processed pseudogenes that localize to chromosomes 1 and 13, respectively, have been reported. [provided by RefSeq, May 2011]","start":12785478,"end":12929643,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 2 [Source:HGNC Symbol;Acc:HGNC:9650]"}, {"versioned_ensembl_gene_id":"ENSG00000279987.1","gene_symbol":"AC008103.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18883502,"end":18884682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274977.1","gene_symbol":"AC011298.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":240701204,"end":240701685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229834.1","gene_symbol":"AL354676.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29636486,"end":29636853,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123213.22","gene_symbol":"NLN","gene_name":"neurolysin [Source:HGNC Symbol;Acc:HGNC:16058]","synonyms":"KIAA1226,AGTBP","biotype":"protein_coding","ncbi_id":"57486","summary":"This gene encodes a member of the metallopeptidase M3 protein family that cleaves neurotensin at the Pro10-Tyr11 bond, leading to the formation of neurotensin(1-10) and neurotensin(11-13). The encoded protein is likely involved in the termination of the neurotensinergic signal in the central nervous system and in the gastrointestinal tract.[provided by RefSeq, Jun 2010]","start":65722196,"end":65871725,"strand":1,"description":"neurolysin [Source:HGNC Symbol;Acc:HGNC:16058]"}, {"versioned_ensembl_gene_id":"ENSG00000277047.4","gene_symbol":"AL390964.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54940843,"end":54986719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231976.8","gene_symbol":"FAM238B","gene_name":"family with sequence similarity 238 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44917]","synonyms":"LINC00202-2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"731789","summary":null,"start":26647986,"end":26653454,"strand":1,"description":"family with sequence similarity 238 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:44917]"}, {"versioned_ensembl_gene_id":"ENSG00000230347.5","gene_symbol":"CT47A8","gene_name":"cancer/testis antigen family 47, member A8 [Source:HGNC Symbol;Acc:HGNC:33289]","synonyms":"CT47.8","biotype":"protein_coding","ncbi_id":"728049","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120948422,"end":120951744,"strand":-1,"description":"cancer/testis antigen family 47, member A8 [Source:HGNC Symbol;Acc:HGNC:33289]"}, {"versioned_ensembl_gene_id":"ENSG00000274807.4","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832788,"end":54848156,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000273643.1","gene_symbol":"PPP1R26P2","gene_name":"protein phosphatase 1 regulatory subunit 26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42016]","synonyms":"KIAA0649P2","biotype":"processed_pseudogene","ncbi_id":"100133064","summary":null,"start":18650023,"end":18653617,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 26 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42016]"}, {"versioned_ensembl_gene_id":"ENSG00000231947.1","gene_symbol":"MTND2P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42125]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873230","summary":null,"start":55179194,"end":55179999,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42125]"}, {"versioned_ensembl_gene_id":"ENSG00000235696.8","gene_symbol":"C2","gene_name":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]","synonyms":null,"biotype":"protein_coding","ncbi_id":"717","summary":"Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]","start":31912644,"end":31938328,"strand":1,"description":"complement C2 [Source:HGNC Symbol;Acc:HGNC:1248]"}, {"versioned_ensembl_gene_id":"ENSG00000234296.1","gene_symbol":"AL390961.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26643228,"end":26645016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236873.9","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32235221,"end":32245105,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000241839.9","gene_symbol":"PLEKHO2","gene_name":"pleckstrin homology domain containing O2 [Source:HGNC Symbol;Acc:HGNC:30026]","synonyms":"pp9099,PP1628,PLEKHQ1,DKFZp761K2312","biotype":"protein_coding","ncbi_id":"80301","summary":null,"start":64841883,"end":64868007,"strand":1,"description":"pleckstrin homology domain containing O2 [Source:HGNC Symbol;Acc:HGNC:30026]"}, {"versioned_ensembl_gene_id":"ENSG00000235885.7","gene_symbol":"LINC01828","gene_name":"long intergenic non-protein coding RNA 1828 [Source:HGNC Symbol;Acc:HGNC:52634]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102800447","summary":null,"start":67086446,"end":67311439,"strand":1,"description":"long intergenic non-protein coding RNA 1828 [Source:HGNC Symbol;Acc:HGNC:52634]"}, {"versioned_ensembl_gene_id":"ENSG00000213423.4","gene_symbol":"RBMX2P2","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132808","summary":null,"start":141261119,"end":141264213,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39924]"}, {"versioned_ensembl_gene_id":"ENSG00000240591.1","gene_symbol":"AL096701.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31454251,"end":31464204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229169.1","gene_symbol":"AL096701.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31538352,"end":31538589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215068.7","gene_symbol":"AC025171.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43041575,"end":43045390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243981.4","gene_symbol":"AC064862.6","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":57628479,"end":57645189,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237396.1","gene_symbol":"LINC01384","gene_name":"long intergenic non-protein coding RNA 1384 [Source:HGNC Symbol;Acc:HGNC:50656]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929685","summary":null,"start":22587522,"end":22607517,"strand":-1,"description":"long intergenic non-protein coding RNA 1384 [Source:HGNC Symbol;Acc:HGNC:50656]"}, {"versioned_ensembl_gene_id":"ENSG00000226929.3","gene_symbol":"CT47A11","gene_name":"cancer/testis antigen family 47, member A11 [Source:HGNC Symbol;Acc:HGNC:27397]","synonyms":"CT47.11","biotype":"protein_coding","ncbi_id":"255313","summary":"This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24. [provided by RefSeq, Sep 2010]","start":120933840,"end":120937158,"strand":-1,"description":"cancer/testis antigen family 47, member A11 [Source:HGNC Symbol;Acc:HGNC:27397]"}, {"versioned_ensembl_gene_id":"ENSG00000237563.1","gene_symbol":"TTTY21B","gene_name":"testis-specific transcript, Y-linked 21B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37980]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100101115","summary":null,"start":6443434,"end":6447077,"strand":1,"description":"testis-specific transcript, Y-linked 21B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:37980]"}, {"versioned_ensembl_gene_id":"ENSG00000229605.5","gene_symbol":"RPL21P93","gene_name":"ribosomal protein L21 pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:35646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653665","summary":null,"start":28898996,"end":28899484,"strand":-1,"description":"ribosomal protein L21 pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:35646]"}, {"versioned_ensembl_gene_id":"ENSG00000276508.1","gene_symbol":"AC243830.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36684754,"end":36685129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122958.14","gene_symbol":"VPS26A","gene_name":"VPS26, retromer complex component A [Source:HGNC Symbol;Acc:HGNC:12711]","synonyms":"VPS26,PEP8A,Hbeta58","biotype":"protein_coding","ncbi_id":"9559","summary":"This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the retromer complex, involved in retrograde transport of proteins from endosomes to the trans-Golgi network. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with VPS35, which serves as the core of the retromer complex. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":69123512,"end":69172861,"strand":1,"description":"VPS26, retromer complex component A [Source:HGNC Symbol;Acc:HGNC:12711]"}, {"versioned_ensembl_gene_id":"ENSG00000169895.5","gene_symbol":"SYAP1","gene_name":"synapse associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16273]","synonyms":"PRO3113,FLJ14495","biotype":"protein_coding","ncbi_id":"94056","summary":null,"start":16719632,"end":16765336,"strand":1,"description":"synapse associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16273]"}, {"versioned_ensembl_gene_id":"ENSG00000282322.1","gene_symbol":"IGHV3-11","gene_name":"immunoglobulin heavy variable 3-11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5580]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28450","summary":null,"start":106117406,"end":106117975,"strand":-1,"description":"immunoglobulin heavy variable 3-11 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5580]"}, {"versioned_ensembl_gene_id":"ENSG00000260786.1","gene_symbol":"AC108099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42188266,"end":42191523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173473.10","gene_symbol":"SMARCC1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 [Source:HGNC Symbol;Acc:HGNC:11104]","synonyms":"SRG3,Rsc8,CRACC1,BAF155","biotype":"protein_coding","ncbi_id":"6599","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and contains a predicted leucine zipper motif typical of many transcription factors. [provided by RefSeq, Jul 2008]","start":47585272,"end":47782106,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 [Source:HGNC Symbol;Acc:HGNC:11104]"}, {"versioned_ensembl_gene_id":"ENSG00000177311.11","gene_symbol":"ZBTB38","gene_name":"zinc finger and BTB domain containing 38 [Source:HGNC Symbol;Acc:HGNC:26636]","synonyms":"PPP1R171,FLJ35036,CIBZ,ZNF921","biotype":"protein_coding","ncbi_id":"253461","summary":"The protein encoded by this gene is a zinc finger transcriptional activator that binds methylated DNA. The encoded protein can form homodimers or heterodimers through the zinc finger domains. In mouse, inhibition of this protein has been associated with apoptosis in some cell types. [provided by RefSeq, Jun 2010]","start":141324213,"end":141449792,"strand":1,"description":"zinc finger and BTB domain containing 38 [Source:HGNC Symbol;Acc:HGNC:26636]"}, {"versioned_ensembl_gene_id":"ENSG00000273582.1","gene_symbol":"AC009093.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29225594,"end":29226348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272630.1","gene_symbol":"AL731563.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73098044,"end":73101297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102144.13","gene_symbol":"PGK1","gene_name":"phosphoglycerate kinase 1 [Source:HGNC Symbol;Acc:HGNC:8896]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5230","summary":"The protein encoded by this gene is a glycolytic enzyme that catalyzes the conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate. The encoded protein may also act as a cofactor for polymerase alpha. Additionally, this protein is secreted by tumor cells where it participates in angiogenesis by functioning to reduce disulfide bonds in the serine protease, plasmin, which consequently leads to the release of the tumor blood vessel inhibitor angiostatin. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Deficiency of the enzyme is associated with a wide range of clinical phenotypes hemolytic anemia and neurological impairment. Pseudogenes of this gene have been defined on chromosomes 19, 21 and the X chromosome. [provided by RefSeq, Jan 2014]","start":78065188,"end":78129296,"strand":1,"description":"phosphoglycerate kinase 1 [Source:HGNC Symbol;Acc:HGNC:8896]"}, {"versioned_ensembl_gene_id":"ENSG00000241399.6","gene_symbol":"CD302","gene_name":"CD302 molecule [Source:HGNC Symbol;Acc:HGNC:30843]","synonyms":"KIAA0022,DCL-1,CLEC13A,BIMLEC","biotype":"protein_coding","ncbi_id":"9936","summary":"CD302 is a C-type lectin receptor involved in cell adhesion and migration, as well as endocytosis and phagocytosis (Kato et al., 2007 [PubMed 17947679]).[supplied by OMIM, Aug 2008]","start":159768630,"end":159798255,"strand":-1,"description":"CD302 molecule [Source:HGNC Symbol;Acc:HGNC:30843]"}, {"versioned_ensembl_gene_id":"ENSG00000204949.8","gene_symbol":"FAM83A-AS1","gene_name":"FAM83A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48658]","synonyms":"HCCC11","biotype":"antisense_RNA","ncbi_id":"100131726","summary":null,"start":123201172,"end":123202743,"strand":-1,"description":"FAM83A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48658]"}, {"versioned_ensembl_gene_id":"ENSG00000275774.2","gene_symbol":"HNRNPCL2","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]","synonyms":"HNRNPCP5,HNRNPCP5","biotype":"protein_coding","ncbi_id":"440563","summary":null,"start":13115496,"end":13116854,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]"}, {"versioned_ensembl_gene_id":"ENSG00000229679.1","gene_symbol":"AC007327.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36229280,"end":36231107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213055.3","gene_symbol":"EEF1B2P7","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421756","summary":null,"start":232729523,"end":232730198,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51454]"}, {"versioned_ensembl_gene_id":"ENSG00000234466.1","gene_symbol":"AL590240.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55054945,"end":55055838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228770.1","gene_symbol":"AC007327.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36228621,"end":36228884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274354.1","gene_symbol":"AC105105.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58511598,"end":58512310,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280739.2","gene_symbol":"EIF1B-AS1","gene_name":"EIF1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44555]","synonyms":"FLJ33065","biotype":"processed_transcript","ncbi_id":"440952","summary":null,"start":40173145,"end":40309698,"strand":-1,"description":"EIF1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44555]"}, {"versioned_ensembl_gene_id":"ENSG00000282118.1","gene_symbol":"AC243913.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28614840,"end":28614963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230377.1","gene_symbol":"ELOCP7","gene_name":"elongin C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38143]","synonyms":"TCEB1P7","biotype":"processed_pseudogene","ncbi_id":"100462868","summary":null,"start":18532326,"end":18532656,"strand":-1,"description":"elongin C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:38143]"}, {"versioned_ensembl_gene_id":"ENSG00000109332.19","gene_symbol":"UBE2D3","gene_name":"ubiquitin conjugating enzyme E2 D3 [Source:HGNC Symbol;Acc:HGNC:12476]","synonyms":"UbcH5C","biotype":"protein_coding","ncbi_id":"7323","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme functions in the ubiquitination of the tumor-suppressor protein p53, which is induced by an E3 ubiquitin-protein ligase. [provided by RefSeq, Jan 2017]","start":102794383,"end":102868896,"strand":-1,"description":"ubiquitin conjugating enzyme E2 D3 [Source:HGNC Symbol;Acc:HGNC:12476]"}, {"versioned_ensembl_gene_id":"ENSG00000227655.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30712087,"end":30712353,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000223939.8","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32969856,"end":32970532,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000139914.6","gene_symbol":"FITM1","gene_name":"fat storage inducing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:33714]","synonyms":"FIT1","biotype":"protein_coding","ncbi_id":"161247","summary":"FIT1 belongs to an evolutionarily conserved family of proteins involved in fat storage (Kadereit et al., 2008 [PubMed 18160536]).[supplied by OMIM, May 2008]","start":24131275,"end":24132849,"strand":1,"description":"fat storage inducing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:33714]"}, {"versioned_ensembl_gene_id":"ENSG00000138658.15","gene_symbol":"ZGRF1","gene_name":"zinc finger GRF-type containing 1 [Source:HGNC Symbol;Acc:HGNC:25654]","synonyms":"FLJ11331,C4orf21","biotype":"protein_coding","ncbi_id":"55345","summary":"The encoded protein contains GRF zinc finger (zf-GRF) and transmembrane domains. GRF zinc fingers are found in a number of DNA-binding proteins. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]","start":112539333,"end":112636995,"strand":-1,"description":"zinc finger GRF-type containing 1 [Source:HGNC Symbol;Acc:HGNC:25654]"}, {"versioned_ensembl_gene_id":"ENSG00000282745.1","gene_symbol":"IGHV6-1","gene_name":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28385","summary":null,"start":105940525,"end":105941024,"strand":-1,"description":"immunoglobulin heavy variable 6-1 [Source:HGNC Symbol;Acc:HGNC:5662]"}, {"versioned_ensembl_gene_id":"ENSG00000276205.1","gene_symbol":"AL603758.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131221196,"end":131221436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197037.10","gene_symbol":"ZSCAN25","gene_name":"zinc finger and SCAN domain containing 25 [Source:HGNC Symbol;Acc:HGNC:21961]","synonyms":"ZNF498,FLJ32468","biotype":"protein_coding","ncbi_id":"221785","summary":"This gene encodes a protein that bears some similarity to zinc finger proteins, which are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants have been identified, but the full-length nature for most of them has not been determined. [provided by RefSeq, Jul 2008]","start":99616946,"end":99632407,"strand":1,"description":"zinc finger and SCAN domain containing 25 [Source:HGNC Symbol;Acc:HGNC:21961]"}, {"versioned_ensembl_gene_id":"ENSG00000281704.1","gene_symbol":"AC226496.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68783385,"end":68789360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117399.13","gene_symbol":"CDC20","gene_name":"cell division cycle 20 [Source:HGNC Symbol;Acc:HGNC:1723]","synonyms":"p55CDC,CDC20A","biotype":"protein_coding","ncbi_id":"991","summary":"CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. It is required for two microtubule-dependent processes, nuclear movement prior to anaphase and chromosome separation. [provided by RefSeq, Jul 2008]","start":43358955,"end":43363203,"strand":1,"description":"cell division cycle 20 [Source:HGNC Symbol;Acc:HGNC:1723]"}, {"versioned_ensembl_gene_id":"ENSG00000280408.1","gene_symbol":"AC032044.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1352070,"end":1352255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278462.1","gene_symbol":"AL359880.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46717423,"end":46717688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155070.8","gene_symbol":"UNC93B2","gene_name":"unc-93 homolog B2 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13482]","synonyms":"UNC93B2P","biotype":"processed_pseudogene","ncbi_id":"641922","summary":null,"start":6855485,"end":6859830,"strand":-1,"description":"unc-93 homolog B2 pseudogene (C. elegans) [Source:HGNC Symbol;Acc:HGNC:13482]"}, {"versioned_ensembl_gene_id":"ENSG00000213959.2","gene_symbol":"AL035419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38614913,"end":38615476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151150.21","gene_symbol":"ANK3","gene_name":"ankyrin 3 [Source:HGNC Symbol;Acc:HGNC:494]","synonyms":null,"biotype":"protein_coding","ncbi_id":"288","summary":"Ankyrins are a family of proteins that are believed to link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact, and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 3 is an immunologically distinct gene product from ankyrins 1 and 2, and was originally found at the axonal initial segment and nodes of Ranvier of neurons in the central and peripheral nervous systems. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]","start":60026298,"end":60733490,"strand":-1,"description":"ankyrin 3 [Source:HGNC Symbol;Acc:HGNC:494]"}, {"versioned_ensembl_gene_id":"ENSG00000233915.4","gene_symbol":"UBE2Q2P10","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49518]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101928256","summary":null,"start":86660525,"end":86661922,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49518]"}, {"versioned_ensembl_gene_id":"ENSG00000243321.3","gene_symbol":"LINC01998","gene_name":"long intergenic non-protein coding RNA 1998 [Source:HGNC Symbol;Acc:HGNC:52832]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986046","summary":null,"start":150077494,"end":150080117,"strand":-1,"description":"long intergenic non-protein coding RNA 1998 [Source:HGNC Symbol;Acc:HGNC:52832]"}, {"versioned_ensembl_gene_id":"ENSG00000115884.10","gene_symbol":"SDC1","gene_name":"syndecan 1 [Source:HGNC Symbol;Acc:HGNC:10658]","synonyms":"syndecan,SYND1,SDC,CD138","biotype":"protein_coding","ncbi_id":"6382","summary":"The protein encoded by this gene is a transmembrane (type I) heparan sulfate proteoglycan and is a member of the syndecan proteoglycan family. The syndecans mediate cell binding, cell signaling, and cytoskeletal organization and syndecan receptors are required for internalization of the HIV-1 tat protein. The syndecan-1 protein functions as an integral membrane protein and participates in cell proliferation, cell migration and cell-matrix interactions via its receptor for extracellular matrix proteins. Altered syndecan-1 expression has been detected in several different tumor types. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same protein. [provided by RefSeq, Jul 2008]","start":20200797,"end":20225433,"strand":-1,"description":"syndecan 1 [Source:HGNC Symbol;Acc:HGNC:10658]"}, {"versioned_ensembl_gene_id":"ENSG00000226747.6","gene_symbol":"AC007966.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":185719874,"end":185740479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111186.12","gene_symbol":"WNT5B","gene_name":"Wnt family member 5B [Source:HGNC Symbol;Acc:HGNC:16265]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81029","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 94% and 80% amino acid identity to the mouse Wnt5b protein and the human WNT5A protein, respectively. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]","start":1529891,"end":1647243,"strand":1,"description":"Wnt family member 5B [Source:HGNC Symbol;Acc:HGNC:16265]"}, {"versioned_ensembl_gene_id":"ENSG00000233933.2","gene_symbol":"AL135924.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72275453,"end":72275973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182601.6","gene_symbol":"HS3ST4","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:5200]","synonyms":"3OST4","biotype":"protein_coding","ncbi_id":"9951","summary":"This gene encodes the enzyme heparan sulfate D-glucosaminyl 3-O-sulfotransferase 4. This enzyme generates 3-O-sulfated glucosaminyl residues in heparan sulfate. Cell surface heparan sulfate is used as a receptor by herpes simplex virus type 1 (HSV-1), and expression of this gene is thought to play a role in HSV-1 pathogenesis. [provided by RefSeq, Jul 2008]","start":25692026,"end":26137688,"strand":1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:5200]"}, {"versioned_ensembl_gene_id":"ENSG00000260690.1","gene_symbol":"CYCSP39","gene_name":"cytochrome c, somatic pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:24412]","synonyms":"HCP39,HC1","biotype":"processed_pseudogene","ncbi_id":"342358","summary":null,"start":25454339,"end":25454647,"strand":-1,"description":"cytochrome c, somatic pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:24412]"}, {"versioned_ensembl_gene_id":"ENSG00000282010.1","gene_symbol":"IGHD6-6","gene_name":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]","synonyms":"IGHD66,D(N4)","biotype":"IG_D_gene","ncbi_id":"28488","summary":null,"start":105911181,"end":105911198,"strand":-1,"description":"immunoglobulin heavy diversity 6-6 [Source:HGNC Symbol;Acc:HGNC:5517]"}, {"versioned_ensembl_gene_id":"ENSG00000224481.1","gene_symbol":"AC245100.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148328999,"end":148344636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234556.1","gene_symbol":"LINC00701","gene_name":"long intergenic non-protein coding RNA 701 [Source:HGNC Symbol;Acc:HGNC:44674]","synonyms":null,"biotype":"lincRNA","ncbi_id":"399708","summary":null,"start":2305083,"end":2315075,"strand":-1,"description":"long intergenic non-protein coding RNA 701 [Source:HGNC Symbol;Acc:HGNC:44674]"}, {"versioned_ensembl_gene_id":"ENSG00000110876.9","gene_symbol":"SELPLG","gene_name":"selectin P ligand [Source:HGNC Symbol;Acc:HGNC:10722]","synonyms":"PSGL-1,CD162","biotype":"protein_coding","ncbi_id":"6404","summary":"This gene encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-, E- and L- selectin expressed on myeloid cells and stimulated T lymphocytes. As such, this protein plays a critical role in leukocyte trafficking during inflammation by tethering of leukocytes to activated platelets or endothelia expressing selectins. This protein requires two post-translational modifications, tyrosine sulfation and the addition of the sialyl Lewis x tetrasaccharide (sLex) to its O-linked glycans, for its high-affinity binding activity. Aberrant expression of this gene and polymorphisms in this gene are associated with defects in the innate and adaptive immune response. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011]","start":108622277,"end":108633959,"strand":-1,"description":"selectin P ligand [Source:HGNC Symbol;Acc:HGNC:10722]"}, {"versioned_ensembl_gene_id":"ENSG00000264176.1","gene_symbol":"MAGOH2P","gene_name":"mago homolog 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:30148]","synonyms":"MAGOH2","biotype":"transcribed_processed_pseudogene","ncbi_id":"100506898","summary":null,"start":10716002,"end":10716511,"strand":-1,"description":"mago homolog 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:30148]"}, {"versioned_ensembl_gene_id":"ENSG00000280471.1","gene_symbol":"FAM90A6P","gene_name":"family with sequence similarity 90 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32254]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"389618","summary":null,"start":7541029,"end":7544038,"strand":-1,"description":"family with sequence similarity 90 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:32254]"}, {"versioned_ensembl_gene_id":"ENSG00000261730.1","gene_symbol":"AL034346.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1383790,"end":1385066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281809.1","gene_symbol":"AL499606.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1321698,"end":1324022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240012.1","gene_symbol":"SLC9A9-AS1","gene_name":"SLC9A9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40928]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885796","summary":null,"start":143342246,"end":143347071,"strand":1,"description":"SLC9A9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40928]"}, {"versioned_ensembl_gene_id":"ENSG00000230946.3","gene_symbol":"HNRNPA1P68","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:48798]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421397","summary":null,"start":100941017,"end":100941995,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:48798]"}, {"versioned_ensembl_gene_id":"ENSG00000262679.1","gene_symbol":"APOBEC3B-AS1","gene_name":"APOBEC3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43836]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874530","summary":null,"start":38961611,"end":38968270,"strand":-1,"description":"APOBEC3B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43836]"}, {"versioned_ensembl_gene_id":"ENSG00000282135.1","gene_symbol":"AC246787.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105890855,"end":105897348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145388.14","gene_symbol":"METTL14","gene_name":"methyltransferase like 14 [Source:HGNC Symbol;Acc:HGNC:29330]","synonyms":"KIAA1627","biotype":"protein_coding","ncbi_id":"57721","summary":null,"start":118685368,"end":118715433,"strand":1,"description":"methyltransferase like 14 [Source:HGNC Symbol;Acc:HGNC:29330]"}, {"versioned_ensembl_gene_id":"ENSG00000227465.1","gene_symbol":"GPN3P1","gene_name":"GPN-loop GTPase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100302689","summary":null,"start":25647570,"end":25648104,"strand":-1,"description":"GPN-loop GTPase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44914]"}, {"versioned_ensembl_gene_id":"ENSG00000248993.1","gene_symbol":"AL645941.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32937364,"end":32953122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105926.15","gene_symbol":"MPP6","gene_name":"membrane palmitoylated protein 6 [Source:HGNC Symbol;Acc:HGNC:18167]","synonyms":"VAM-1,PALS2,p55T","biotype":"protein_coding","ncbi_id":"51678","summary":"Members of the peripheral membrane-associated guanylate kinase (MAGUK) family function in tumor suppression and receptor clustering by forming multiprotein complexes containing distinct sets of transmembrane, cytoskeletal, and cytoplasmic signaling proteins. All MAGUKs contain a PDZ-SH3-GUK core and are divided into 4 subfamilies, DLG-like (see DLG1; MIM 601014), ZO1-like (see TJP1; MIM 601009), p55-like (see MPP1; MIM 305360), and LIN2-like (see CASK; MIM 300172), based on their size and the presence of additional domains. MPP6 is a member of the p55-like MAGUK subfamily (Tseng et al., 2001 [PubMed 11311936]).[supplied by OMIM, Mar 2008]","start":24573268,"end":24694193,"strand":1,"description":"membrane palmitoylated protein 6 [Source:HGNC Symbol;Acc:HGNC:18167]"}, {"versioned_ensembl_gene_id":"ENSG00000206240.11","gene_symbol":"HLA-DRB1","gene_name":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]","synonyms":"HLA-DR1B","biotype":"protein_coding","ncbi_id":"3123","summary":"HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020]","start":32508164,"end":32538771,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 1 [Source:HGNC Symbol;Acc:HGNC:4948]"}, {"versioned_ensembl_gene_id":"ENSG00000220139.1","gene_symbol":"AL022722.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119159297,"end":119159476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257513.7","gene_symbol":"NPIPB1P","gene_name":"nuclear pore complex interacting protein family member B1, pseudogene [Source:HGNC Symbol;Acc:HGNC:37452]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729602","summary":null,"start":11619509,"end":11639699,"strand":-1,"description":"nuclear pore complex interacting protein family member B1, pseudogene [Source:HGNC Symbol;Acc:HGNC:37452]"}, {"versioned_ensembl_gene_id":"ENSG00000177106.14","gene_symbol":"EPS8L2","gene_name":"EPS8 like 2 [Source:HGNC Symbol;Acc:HGNC:21296]","synonyms":"FLJ22171,FLJ21935,MGC3088","biotype":"protein_coding","ncbi_id":"64787","summary":"This gene encodes a member of the EPS8 gene family. The encoded protein, like other members of the family, is thought to link growth factor stimulation to actin organization, generating functional redundancy in the pathways that regulate actin cytoskeletal remodeling. [provided by RefSeq, Dec 2008]","start":694438,"end":727727,"strand":1,"description":"EPS8 like 2 [Source:HGNC Symbol;Acc:HGNC:21296]"}, {"versioned_ensembl_gene_id":"ENSG00000231326.6","gene_symbol":"AL441943.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2169140,"end":2189474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271157.1","gene_symbol":"AL022154.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88827554,"end":88829858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263290.5","gene_symbol":"SCAMP3","gene_name":"secretory carrier membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:10565]","synonyms":"C1orf3","biotype":"protein_coding","ncbi_id":"10067","summary":"This gene encodes an integral membrane protein that belongs to the secretory carrier membrane protein family. The encoded protein functions as a carrier to the cell surface in post-golgi recycling pathways. This protein is also involved in protein trafficking in endosomal pathways. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":155271383,"end":155277834,"strand":-1,"description":"secretory carrier membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:10565]"}, {"versioned_ensembl_gene_id":"ENSG00000234515.1","gene_symbol":"PPP1R2P1","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]","synonyms":"PPP1R2P,IPP-2P","biotype":"transcribed_processed_pseudogene","ncbi_id":"100507444","summary":null,"start":32879171,"end":32879848,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9289]"}, {"versioned_ensembl_gene_id":"ENSG00000235095.1","gene_symbol":"AC099654.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57147986,"end":57150347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235923.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"Em:AB023053.1,TRIM26P1,TRIM26P","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30227804,"end":30231780,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000273434.1","gene_symbol":"AC090115.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":48417150,"end":48417337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280428.1","gene_symbol":"BNIP3P24","gene_name":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421698","summary":null,"start":20784596,"end":20785152,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:49704]"}, {"versioned_ensembl_gene_id":"ENSG00000100982.11","gene_symbol":"PCIF1","gene_name":"PDX1 C-terminal inhibiting factor 1 [Source:HGNC Symbol;Acc:HGNC:16200]","synonyms":"PPP1R121,C20orf67,bA465L10.1","biotype":"protein_coding","ncbi_id":"63935","summary":null,"start":45934628,"end":45948023,"strand":1,"description":"PDX1 C-terminal inhibiting factor 1 [Source:HGNC Symbol;Acc:HGNC:16200]"}, {"versioned_ensembl_gene_id":"ENSG00000244701.1","gene_symbol":"AC004918.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141652381,"end":141656810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179943.7","gene_symbol":"FIZ1","gene_name":"FLT3 interacting zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:25917]","synonyms":"ZNF798,FLJ14768","biotype":"protein_coding","ncbi_id":"84922","summary":"This gene encodes zinc finger protein, which interacts with a receptor tyrosine kinase involved in the regulation of hematopoietic and lymphoid cells. This gene product also interacts with a transcription factor that regulates the expression of rod-specific genes in retina. [provided by RefSeq, Jul 2008]","start":55591371,"end":55601970,"strand":-1,"description":"FLT3 interacting zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:25917]"}, {"versioned_ensembl_gene_id":"ENSG00000234741.7","gene_symbol":"GAS5","gene_name":"growth arrest specific 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16355]","synonyms":"SNHG2,NCRNA00030","biotype":"processed_transcript","ncbi_id":"60674","summary":"This gene produces a spliced long non-coding RNA and is a member of the 5' terminal oligo-pyrimidine class of genes. It is a small nucleolar RNA host gene, containing multiple C/D box snoRNA genes in its introns. Part of the secondary RNA structure of the encoded transcript mimics glucocorticoid response element (GRE) which means it can bind to the DNA binding domain of the glucocorticoid receptor (nuclear receptor subfamily 3, group C, member 1). This action blocks the glucocorticoid receptor from being activated and thereby stops it from regulating the transcription of its target genes. This transcript is also thought to regulate the transcriptional activity of other receptors, such as androgen, progesterone and mineralocorticoid receptors, that can bind to its GRE mimic region. Multiple functions have been associated with this transcript, including cellular growth arrest and apoptosis. It has also been identified as a potential tumor suppressor, with its down-regulation associated with cancer in multiple different tissues. [provided by RefSeq, Mar 2015]","start":173863900,"end":173868882,"strand":-1,"description":"growth arrest specific 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16355]"}, {"versioned_ensembl_gene_id":"ENSG00000241313.2","gene_symbol":"WWTR1-AS1","gene_name":"WWTR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41035]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128025","summary":null,"start":149657020,"end":149661364,"strand":1,"description":"WWTR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41035]"}, {"versioned_ensembl_gene_id":"ENSG00000107864.14","gene_symbol":"CPEB3","gene_name":"cytoplasmic polyadenylation element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:21746]","synonyms":"KIAA0940","biotype":"protein_coding","ncbi_id":"22849","summary":null,"start":92046692,"end":92291087,"strand":-1,"description":"cytoplasmic polyadenylation element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:21746]"}, {"versioned_ensembl_gene_id":"ENSG00000224936.1","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"Em:AB014080.4,SUCLA2P","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30468882,"end":30470251,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000249740.2","gene_symbol":"OSMR-AS1","gene_name":"OSMR antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50296]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929768","summary":null,"start":38710367,"end":38845829,"strand":-1,"description":"OSMR antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50296]"}, {"versioned_ensembl_gene_id":"ENSG00000255972.1","gene_symbol":"AC026333.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122563735,"end":122563762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243641.3","gene_symbol":"OR13C7","gene_name":"olfactory receptor family 13 subfamily C member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15102]","synonyms":"OST706,OR13C7P","biotype":"polymorphic_pseudogene","ncbi_id":"81377","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":36002909,"end":36003867,"strand":-1,"description":"olfactory receptor family 13 subfamily C member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15102]"}, {"versioned_ensembl_gene_id":"ENSG00000276378.2","gene_symbol":"DEFB108C","gene_name":"defensin beta 108C [Source:HGNC Symbol;Acc:HGNC:30847]","synonyms":"DEFB108P2","biotype":"unprocessed_pseudogene","ncbi_id":"503837","summary":null,"start":7364723,"end":7369092,"strand":1,"description":"defensin beta 108C [Source:HGNC Symbol;Acc:HGNC:30847]"}, {"versioned_ensembl_gene_id":"ENSG00000240499.7","gene_symbol":"AC004594.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":122328469,"end":122440388,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215049.3","gene_symbol":"PRDX2P1","gene_name":"peroxiredoxin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30020]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359844","summary":null,"start":30296147,"end":30296735,"strand":1,"description":"peroxiredoxin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30020]"}, {"versioned_ensembl_gene_id":"ENSG00000264924.1","gene_symbol":"AC090772.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24113637,"end":24121003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259710.1","gene_symbol":"NUTF2P6","gene_name":"nuclear transport factor 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131623","summary":null,"start":35282596,"end":35282980,"strand":1,"description":"nuclear transport factor 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:50455]"}, {"versioned_ensembl_gene_id":"ENSG00000224858.5","gene_symbol":"RPL29P11","gene_name":"ribosomal protein L29 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36905]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131713","summary":null,"start":37016523,"end":37017014,"strand":-1,"description":"ribosomal protein L29 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36905]"}, {"versioned_ensembl_gene_id":"ENSG00000277146.1","gene_symbol":"AC013734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26453982,"end":26454092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188399.5","gene_symbol":"ANKRD36P1","gene_name":"ankyrin repeat domain 36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37759]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132420","summary":null,"start":26409815,"end":26420535,"strand":1,"description":"ankyrin repeat domain 36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37759]"}, {"versioned_ensembl_gene_id":"ENSG00000237923.1","gene_symbol":"AL662797.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30839526,"end":30848159,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177875.4","gene_symbol":"CCDC184","gene_name":"coiled-coil domain containing 184 [Source:HGNC Symbol;Acc:HGNC:33749]","synonyms":"LOC387856,C12orf68","biotype":"protein_coding","ncbi_id":"387856","summary":null,"start":48183584,"end":48185926,"strand":1,"description":"coiled-coil domain containing 184 [Source:HGNC Symbol;Acc:HGNC:33749]"}, {"versioned_ensembl_gene_id":"ENSG00000137331.11","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30743199,"end":30744554,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000188803.14","gene_symbol":"SHISA6","gene_name":"shisa family member 6 [Source:HGNC Symbol;Acc:HGNC:34491]","synonyms":"FLJ45455","biotype":"protein_coding","ncbi_id":"388336","summary":null,"start":11241263,"end":11564063,"strand":1,"description":"shisa family member 6 [Source:HGNC Symbol;Acc:HGNC:34491]"}, {"versioned_ensembl_gene_id":"ENSG00000256667.6","gene_symbol":"KLRA1P","gene_name":"killer cell lectin like receptor A1, pseudogene [Source:HGNC Symbol;Acc:HGNC:6372]","synonyms":"LY49L,Ly49,KLRAP1,KLRA1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10748","summary":null,"start":10588063,"end":10599669,"strand":-1,"description":"killer cell lectin like receptor A1, pseudogene [Source:HGNC Symbol;Acc:HGNC:6372]"}, {"versioned_ensembl_gene_id":"ENSG00000258555.6","gene_symbol":"SPECC1L-ADORA2A","gene_name":"SPECC1L-ADORA2A readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49185]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101730217","summary":"This locus represents naturally occurring readthrough transcription between the neighboring SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1-like) and ADORA2A (adenosine A2a receptor) genes on chromosome 22. The readthrough transcript is a candidate for nonsense-mediated mRNA decay (NMD) and is unlikely to produce a protein product. [provided by RefSeq, Jun 2013]","start":24270898,"end":24442356,"strand":1,"description":"SPECC1L-ADORA2A readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49185]"}, {"versioned_ensembl_gene_id":"ENSG00000144040.12","gene_symbol":"SFXN5","gene_name":"sideroflexin 5 [Source:HGNC Symbol;Acc:HGNC:16073]","synonyms":"BBG-TCC","biotype":"protein_coding","ncbi_id":"94097","summary":null,"start":72942036,"end":73075619,"strand":-1,"description":"sideroflexin 5 [Source:HGNC Symbol;Acc:HGNC:16073]"}, {"versioned_ensembl_gene_id":"ENSG00000135127.11","gene_symbol":"BICDL1","gene_name":"BICD family like cargo adaptor 1 [Source:HGNC Symbol;Acc:HGNC:28095]","synonyms":"FLJ26450,CCDC64,BICDR-1","biotype":"protein_coding","ncbi_id":"92558","summary":null,"start":119989869,"end":120094494,"strand":1,"description":"BICD family like cargo adaptor 1 [Source:HGNC Symbol;Acc:HGNC:28095]"}, {"versioned_ensembl_gene_id":"ENSG00000241328.1","gene_symbol":"LINC02070","gene_name":"long intergenic non-protein coding RNA 2070 [Source:HGNC Symbol;Acc:HGNC:52916]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927494","summary":null,"start":86481943,"end":86496996,"strand":1,"description":"long intergenic non-protein coding RNA 2070 [Source:HGNC Symbol;Acc:HGNC:52916]"}, {"versioned_ensembl_gene_id":"ENSG00000164532.10","gene_symbol":"TBX20","gene_name":"T-box 20 [Source:HGNC Symbol;Acc:HGNC:11598]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57057","summary":"This gene encodes a T-box family member. The T-box family members share a common DNA binding domain, termed the T-box, and they are transcription factors involved in the regulation of developmental processes. This gene is essential for heart development. Mutations in this gene are associated with diverse cardiac pathologies, including defects in septation, valvulogenesis and cardiomyopathy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":35202430,"end":35254147,"strand":-1,"description":"T-box 20 [Source:HGNC Symbol;Acc:HGNC:11598]"}, {"versioned_ensembl_gene_id":"ENSG00000277068.2","gene_symbol":"KRTAP5-4","gene_name":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]","synonyms":"KRTAP5.4","biotype":"protein_coding","ncbi_id":"387267","summary":null,"start":1626668,"end":1627848,"strand":-1,"description":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]"}, {"versioned_ensembl_gene_id":"ENSG00000243701.5","gene_symbol":"DUBR","gene_name":"DPPA2 upstream binding RNA [Source:HGNC Symbol;Acc:HGNC:48569]","synonyms":"LINC00883","biotype":"lincRNA","ncbi_id":"344595","summary":null,"start":107240692,"end":107326964,"strand":1,"description":"DPPA2 upstream binding RNA [Source:HGNC Symbol;Acc:HGNC:48569]"}, {"versioned_ensembl_gene_id":"ENSG00000151962.7","gene_symbol":"RBM46","gene_name":"RNA binding motif protein 46 [Source:HGNC Symbol;Acc:HGNC:28401]","synonyms":"MGC27016,CT68","biotype":"protein_coding","ncbi_id":"166863","summary":null,"start":154781213,"end":154828813,"strand":1,"description":"RNA binding motif protein 46 [Source:HGNC Symbol;Acc:HGNC:28401]"}, {"versioned_ensembl_gene_id":"ENSG00000270540.1","gene_symbol":"AC093915.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":236367560,"end":236369102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249041.1","gene_symbol":"AC009567.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154754756,"end":154781873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231044.10","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"RDBP,D6S45,RD,RDP,NELF-E","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31939633,"end":31946638,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000236369.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"Em:AB014080.3,TMPOL1","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30456729,"end":30458271,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000173273.15","gene_symbol":"TNKS","gene_name":"tankyrase [Source:HGNC Symbol;Acc:HGNC:11941]","synonyms":"TNKS1,TINF1,TIN1,pART5,PARP5A,PARP-5a","biotype":"protein_coding","ncbi_id":"8658","summary":null,"start":9555914,"end":9782346,"strand":1,"description":"tankyrase [Source:HGNC Symbol;Acc:HGNC:11941]"}, {"versioned_ensembl_gene_id":"ENSG00000001630.15","gene_symbol":"CYP51A1","gene_name":"cytochrome P450 family 51 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2649]","synonyms":"CP51,P450L1,P450-14DM,LDM,CYPL1,CYP51","biotype":"protein_coding","ncbi_id":"1595","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein participates in the synthesis of cholesterol by catalyzing the removal of the 14alpha-methyl group from lanosterol. Homologous genes are found in all three eukaryotic phyla, fungi, plants, and animals, suggesting that this is one of the oldest cytochrome P450 genes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":92112151,"end":92142952,"strand":-1,"description":"cytochrome P450 family 51 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2649]"}, {"versioned_ensembl_gene_id":"ENSG00000230096.1","gene_symbol":"AC022535.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4415305,"end":4426179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130226.16","gene_symbol":"DPP6","gene_name":"dipeptidyl peptidase like 6 [Source:HGNC Symbol;Acc:HGNC:3010]","synonyms":"DPL1,DPPX","biotype":"protein_coding","ncbi_id":"1804","summary":"This gene encodes a single-pass type II membrane protein that is a member of the peptidase S9B family of serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Variations in this gene may be associated with susceptibility to amyotrophic lateral sclerosis and with idiopathic ventricular fibrillation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":153887097,"end":154894285,"strand":1,"description":"dipeptidyl peptidase like 6 [Source:HGNC Symbol;Acc:HGNC:3010]"}, {"versioned_ensembl_gene_id":"ENSG00000069535.13","gene_symbol":"MAOB","gene_name":"monoamine oxidase B [Source:HGNC Symbol;Acc:HGNC:6834]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4129","summary":"The protein encoded by this gene belongs to the flavin monoamine oxidase family. It is a enzyme located in the mitochondrial outer membrane. It catalyzes the oxidative deamination of biogenic and xenobiotic amines and plays an important role in the metabolism of neuroactive and vasoactive amines in the central nervous sysytem and peripheral tissues. This protein preferentially degrades benzylamine and phenylethylamine. [provided by RefSeq, Jul 2008]","start":43766611,"end":43882447,"strand":-1,"description":"monoamine oxidase B [Source:HGNC Symbol;Acc:HGNC:6834]"}, {"versioned_ensembl_gene_id":"ENSG00000278588.1","gene_symbol":"HIST1H2BI","gene_name":"histone cluster 1 H2B family member i [Source:HGNC Symbol;Acc:HGNC:4756]","synonyms":"H2BFK,H2B/k","biotype":"protein_coding","ncbi_id":"8346","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. The protein has antibacterial and antifungal antimicrobial activity. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26272976,"end":26273356,"strand":1,"description":"histone cluster 1 H2B family member i [Source:HGNC Symbol;Acc:HGNC:4756]"}, {"versioned_ensembl_gene_id":"ENSG00000147459.17","gene_symbol":"DOCK5","gene_name":"dedicator of cytokinesis 5 [Source:HGNC Symbol;Acc:HGNC:23476]","synonyms":"FLJ21034","biotype":"protein_coding","ncbi_id":"80005","summary":"This gene encodes a member of the dedicator of cytokinesis protein family. Members of this family act as guanine nucleotide exchange factors for small Rho family G proteins. The protein encoded by this gene is thought to associate with adaptors CRK and CRKL, and function in regulation of intestinal epithelial cell spreading and migration on collagen IV. Similar proteins in mouse and zebrafish also function in myoblast fusion. [provided by RefSeq, Oct 2016]","start":25184723,"end":25418082,"strand":1,"description":"dedicator of cytokinesis 5 [Source:HGNC Symbol;Acc:HGNC:23476]"}, {"versioned_ensembl_gene_id":"ENSG00000119953.12","gene_symbol":"SMNDC1","gene_name":"survival motor neuron domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16900]","synonyms":"TDRD16C,SPF30,SMNR","biotype":"protein_coding","ncbi_id":"10285","summary":"This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]","start":110290730,"end":110304951,"strand":-1,"description":"survival motor neuron domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16900]"}, {"versioned_ensembl_gene_id":"ENSG00000158406.4","gene_symbol":"HIST1H4H","gene_name":"histone cluster 1 H4 family member h [Source:HGNC Symbol;Acc:HGNC:4788]","synonyms":"H4FH,H4/h","biotype":"protein_coding","ncbi_id":"8365","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26277609,"end":26285638,"strand":-1,"description":"histone cluster 1 H4 family member h [Source:HGNC Symbol;Acc:HGNC:4788]"}, {"versioned_ensembl_gene_id":"ENSG00000227101.1","gene_symbol":"AC025822.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4024940,"end":4028394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236990.1","gene_symbol":"AC025822.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4051726,"end":4089013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205885.7","gene_symbol":"C1RL-AS1","gene_name":"C1RL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27461]","synonyms":"MATL2963","biotype":"antisense_RNA","ncbi_id":"283314","summary":null,"start":7108052,"end":7122501,"strand":1,"description":"C1RL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27461]"}, {"versioned_ensembl_gene_id":"ENSG00000233117.2","gene_symbol":"LINC00702","gene_name":"long intergenic non-protein coding RNA 702 [Source:HGNC Symbol;Acc:HGNC:44676]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100652988","summary":null,"start":4201141,"end":4243912,"strand":-1,"description":"long intergenic non-protein coding RNA 702 [Source:HGNC Symbol;Acc:HGNC:44676]"}, {"versioned_ensembl_gene_id":"ENSG00000122678.16","gene_symbol":"POLM","gene_name":"DNA polymerase mu [Source:HGNC Symbol;Acc:HGNC:9185]","synonyms":"Tdt-N","biotype":"protein_coding","ncbi_id":"27434","summary":null,"start":44072247,"end":44082540,"strand":-1,"description":"DNA polymerase mu [Source:HGNC Symbol;Acc:HGNC:9185]"}, {"versioned_ensembl_gene_id":"ENSG00000206376.9","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C,C6orf30","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31870139,"end":31888078,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000139178.10","gene_symbol":"C1RL","gene_name":"complement C1r subcomponent like [Source:HGNC Symbol;Acc:HGNC:21265]","synonyms":"C1RL1,C1r-LP","biotype":"protein_coding","ncbi_id":"51279","summary":null,"start":7089587,"end":7109273,"strand":-1,"description":"complement C1r subcomponent like [Source:HGNC Symbol;Acc:HGNC:21265]"}, {"versioned_ensembl_gene_id":"ENSG00000254413.8","gene_symbol":"CHKB-CPT1B","gene_name":"CHKB-CPT1B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"386593","summary":"The genes CHKB and CPT1B are adjacent on chromosome 22 and read-through transcripts are expressed that include exons from both loci. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to express proteins. [provided by RefSeq, Jun 2009]","start":50568869,"end":50582965,"strand":-1,"description":"CHKB-CPT1B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41998]"}, {"versioned_ensembl_gene_id":"ENSG00000167807.15","gene_symbol":"AC011511.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10305427,"end":10316009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236758.5","gene_symbol":"MTUS2-AS2","gene_name":"MTUS2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40923]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874106","summary":null,"start":29239379,"end":29250554,"strand":-1,"description":"MTUS2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40923]"}, {"versioned_ensembl_gene_id":"ENSG00000269335.5","gene_symbol":"IKBKG","gene_name":"inhibitor of nuclear factor kappa B kinase subunit gamma [Source:HGNC Symbol;Acc:HGNC:5961]","synonyms":"FIP-3,ZC2HC9,NEMO,IP2,IP1,IKK-gamma,Fip3p,FIP3","biotype":"protein_coding","ncbi_id":"8517","summary":"This gene encodes the regulatory subunit of the inhibitor of kappaB kinase (IKK) complex, which activates NF-kappaB resulting in activation of genes involved in inflammation, immunity, cell survival, and other pathways. Mutations in this gene result in incontinentia pigmenti, hypohidrotic ectodermal dysplasia, and several other types of immunodeficiencies. A pseudogene highly similar to this locus is located in an adjacent region of the X chromosome. [provided by RefSeq, Mar 2016]","start":154541199,"end":154565046,"strand":1,"description":"inhibitor of nuclear factor kappa B kinase subunit gamma [Source:HGNC Symbol;Acc:HGNC:5961]"}, {"versioned_ensembl_gene_id":"ENSG00000267673.6","gene_symbol":"FDX2","gene_name":"ferredoxin 2 [Source:HGNC Symbol;Acc:HGNC:30546]","synonyms":"FDX1L,MGC19604","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10310045,"end":10316015,"strand":-1,"description":"ferredoxin 2 [Source:HGNC Symbol;Acc:HGNC:30546]"}, {"versioned_ensembl_gene_id":"ENSG00000164736.5","gene_symbol":"SOX17","gene_name":"SRY-box 17 [Source:HGNC Symbol;Acc:HGNC:18122]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64321","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. [provided by RefSeq, Jul 2008]","start":54457935,"end":54460888,"strand":1,"description":"SRY-box 17 [Source:HGNC Symbol;Acc:HGNC:18122]"}, {"versioned_ensembl_gene_id":"ENSG00000116096.5","gene_symbol":"SPR","gene_name":"sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase) [Source:HGNC Symbol;Acc:HGNC:11257]","synonyms":"SDR38C1","biotype":"protein_coding","ncbi_id":"6697","summary":"This gene encodes an aldo-keto reductase that catalyzes the NADPH-dependent reduction of pteridine derivatives and is important in the biosynthesis of tetrahydrobiopterin (BH4). Mutations in this gene result in DOPA-responsive dystonia due to sepiaterin reductase deficiency. A pseudogene has been identified on chromosome 1. [provided by RefSeq, Jul 2008]","start":72887360,"end":72892158,"strand":1,"description":"sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase) [Source:HGNC Symbol;Acc:HGNC:11257]"}, {"versioned_ensembl_gene_id":"ENSG00000153250.19","gene_symbol":"RBMS1","gene_name":"RNA binding motif single stranded interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9907]","synonyms":"DKFZp564H0764,C2orf12,YC1,SCR2,MSSP-3,MSSP-2,MSSP-1,HCC-4","biotype":"protein_coding","ncbi_id":"5937","summary":"This gene encodes a member of a small family of proteins which bind single stranded DNA/RNA. These proteins are characterized by the presence of two sets of ribonucleoprotein consensus sequence (RNP-CS) that contain conserved motifs, RNP1 and RNP2, originally described in RNA binding proteins, and required for DNA binding. These proteins have been implicated in such diverse functions as DNA replication, gene transcription, cell cycle progression and apoptosis. Several transcript variants, resulting from alternative splicing and encoding different isoforms, have been described. A pseudogene for this locus is found on chromosome 12. [provided by RefSeq, Feb 2009]","start":160272151,"end":160493794,"strand":-1,"description":"RNA binding motif single stranded interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:9907]"}, {"versioned_ensembl_gene_id":"ENSG00000230337.1","gene_symbol":"AL109811.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11099675,"end":11102100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160994.3","gene_symbol":"CCDC105","gene_name":"coiled-coil domain containing 105 [Source:HGNC Symbol;Acc:HGNC:26866]","synonyms":"FLJ40365","biotype":"protein_coding","ncbi_id":"126402","summary":null,"start":15010744,"end":15023269,"strand":1,"description":"coiled-coil domain containing 105 [Source:HGNC Symbol;Acc:HGNC:26866]"}, {"versioned_ensembl_gene_id":"ENSG00000230207.1","gene_symbol":"RPL4P5","gene_name":"ribosomal protein L4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158345","summary":null,"start":7477045,"end":7478320,"strand":-1,"description":"ribosomal protein L4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35699]"}, {"versioned_ensembl_gene_id":"ENSG00000251307.1","gene_symbol":"AC026704.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55233934,"end":55295201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224155.2","gene_symbol":"AC073136.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56304678,"end":56305526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112972.14","gene_symbol":"HMGCS1","gene_name":"3-hydroxy-3-methylglutaryl-CoA synthase 1 [Source:HGNC Symbol;Acc:HGNC:5007]","synonyms":"HMGCS","biotype":"protein_coding","ncbi_id":"3157","summary":null,"start":43289395,"end":43313512,"strand":-1,"description":"3-hydroxy-3-methylglutaryl-CoA synthase 1 [Source:HGNC Symbol;Acc:HGNC:5007]"}, {"versioned_ensembl_gene_id":"ENSG00000115486.11","gene_symbol":"GGCX","gene_name":"gamma-glutamyl carboxylase [Source:HGNC Symbol;Acc:HGNC:4247]","synonyms":"VKCFD1","biotype":"protein_coding","ncbi_id":"2677","summary":"This gene encodes an integral membrane protein of the rough endoplasmic reticulum that carboxylates glutamate residues of vitamin K-dependent proteins to gamma carboxyl glutamate, a modification that is required for their activity. The vitamin K-dependent protein substrates have a propeptide that binds the enzyme, with carbon dioxide, dioxide, and reduced vitamin K acting as co-substrates. Vitamin K-dependent proteins affect a number of physiologic processes including blood coagulation, prevention of vascular calcification, and inflammation. Allelic variants of this gene have been associated with pseudoxanthoma elasticum-like disorder with associated multiple coagulation factor deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]","start":85544723,"end":85561547,"strand":-1,"description":"gamma-glutamyl carboxylase [Source:HGNC Symbol;Acc:HGNC:4247]"}, {"versioned_ensembl_gene_id":"ENSG00000223768.1","gene_symbol":"LINC00205","gene_name":"long intergenic non-protein coding RNA 205 [Source:HGNC Symbol;Acc:HGNC:16420]","synonyms":"NCRNA00205,C21orf86","biotype":"lincRNA","ncbi_id":"102723489","summary":null,"start":45293285,"end":45297354,"strand":1,"description":"long intergenic non-protein coding RNA 205 [Source:HGNC Symbol;Acc:HGNC:16420]"}, {"versioned_ensembl_gene_id":"ENSG00000143373.17","gene_symbol":"ZNF687","gene_name":"zinc finger protein 687 [Source:HGNC Symbol;Acc:HGNC:29277]","synonyms":"KIAA1441","biotype":"protein_coding","ncbi_id":"57592","summary":"This gene encodes C2H2 zinc finger protein. The encoded protein may play a role in bone differentiation and development. Mutations in this gene are the cause of Paget disease of bone-6. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":151281618,"end":151292180,"strand":1,"description":"zinc finger protein 687 [Source:HGNC Symbol;Acc:HGNC:29277]"}, {"versioned_ensembl_gene_id":"ENSG00000276618.4","gene_symbol":"RAD17","gene_name":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]","synonyms":"CCYC,Rad24,RAD17Sp","biotype":"protein_coding","ncbi_id":"5884","summary":"The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This protein shares strong similarity with DNA replication factor C (RFC), and can form a complex with RFCs. This protein binds to chromatin prior to DNA damage and is phosphorylated by the checkpoint kinase ATR following damage. This protein recruits the RAD1-RAD9-HUS1 checkpoint protein complex onto chromatin after DNA damage, which may be required for its phosphorylation. The phosphorylation of this protein is required for the DNA-damage-induced cell cycle G2 arrest, and is thought to be a critical early event during checkpoint signaling in DNA-damaged cells. Multiple alternatively spliced transcript variants of this gene, which encode four distinct protein isoforms, have been reported. Two pseudogenes, located on chromosomes 7 and 13, have been identified. [provided by RefSeq, Jul 2013]","start":69369307,"end":69415042,"strand":1,"description":"RAD17 checkpoint clamp loader component [Source:HGNC Symbol;Acc:HGNC:9807]"}, {"versioned_ensembl_gene_id":"ENSG00000278060.1","gene_symbol":"AC012366.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72932974,"end":72934355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105143.12","gene_symbol":"SLC1A6","gene_name":"solute carrier family 1 member 6 [Source:HGNC Symbol;Acc:HGNC:10944]","synonyms":"EAAT4","biotype":"protein_coding","ncbi_id":"6511","summary":null,"start":14950034,"end":15022990,"strand":-1,"description":"solute carrier family 1 member 6 [Source:HGNC Symbol;Acc:HGNC:10944]"}, {"versioned_ensembl_gene_id":"ENSG00000135638.13","gene_symbol":"EMX1","gene_name":"empty spiracles homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3340]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2016","summary":null,"start":72916260,"end":72936071,"strand":1,"description":"empty spiracles homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3340]"}, {"versioned_ensembl_gene_id":"ENSG00000266728.5","gene_symbol":"AC015688.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":27623364,"end":27640777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140553.17","gene_symbol":"UNC45A","gene_name":"unc-45 myosin chaperone A [Source:HGNC Symbol;Acc:HGNC:30594]","synonyms":"SMAP-1,GC-UNC45","biotype":"protein_coding","ncbi_id":"55898","summary":"This gene encodes a regulatory component of the progesterone receptor/heat shock protein 90 chaperoning complex, which functions in the assembly and folding of the progesterone receptor. The encoded protein is thought to be essential for normal cell proliferation, and for the accumulation of myosin during development of muscle cells. [provided by RefSeq, Sep 2018]","start":90930180,"end":90954093,"strand":1,"description":"unc-45 myosin chaperone A [Source:HGNC Symbol;Acc:HGNC:30594]"}, {"versioned_ensembl_gene_id":"ENSG00000076662.9","gene_symbol":"ICAM3","gene_name":"intercellular adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:5346]","synonyms":"ICAM-R,CDW50,CD50","biotype":"protein_coding","ncbi_id":"3385","summary":"The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein is constitutively and abundantly expressed by all leucocytes and may be the most important ligand for LFA-1 in the initiation of the immune response. It functions not only as an adhesion molecule, but also as a potent signalling molecule. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]","start":10333776,"end":10339823,"strand":-1,"description":"intercellular adhesion molecule 3 [Source:HGNC Symbol;Acc:HGNC:5346]"}, {"versioned_ensembl_gene_id":"ENSG00000185290.3","gene_symbol":"NUPR2","gene_name":"nuclear protein 2, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:44164]","synonyms":"NUPR1L","biotype":"protein_coding","ncbi_id":"389493","summary":null,"start":56114681,"end":56116400,"strand":-1,"description":"nuclear protein 2, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:44164]"}, {"versioned_ensembl_gene_id":"ENSG00000180182.10","gene_symbol":"MED14","gene_name":"mediator complex subunit 14 [Source:HGNC Symbol;Acc:HGNC:2370]","synonyms":"CRSP150,TRAP170,RGR1,EXLM1,CXorf4,CSRP,CRSP2","biotype":"protein_coding","ncbi_id":"9282","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein contains a bipartite nuclear localization signal. This gene is known to escape chromosome X-inactivation. [provided by RefSeq, Jul 2008]","start":40648306,"end":40735858,"strand":-1,"description":"mediator complex subunit 14 [Source:HGNC Symbol;Acc:HGNC:2370]"}, {"versioned_ensembl_gene_id":"ENSG00000225904.1","gene_symbol":"MORF4L1P7","gene_name":"mortality factor 4 like 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39259]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130637","summary":null,"start":176367699,"end":176368401,"strand":-1,"description":"mortality factor 4 like 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39259]"}, {"versioned_ensembl_gene_id":"ENSG00000230191.1","gene_symbol":"AC006970.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56163145,"end":56163533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233028.1","gene_symbol":"AC006970.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56175634,"end":56176412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152953.12","gene_symbol":"STK32B","gene_name":"serine/threonine kinase 32B [Source:HGNC Symbol;Acc:HGNC:14217]","synonyms":"YANK2,STKG6,STK32,HSA250839","biotype":"protein_coding","ncbi_id":"55351","summary":"This gene encodes a serine-threonine protein kinase. Serine-threonine kinases transfer phosphate molecules to the oxygen atoms of serine and threonine. A genomic deletion affecting this gene has been associated with Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":5051442,"end":5500998,"strand":1,"description":"serine/threonine kinase 32B [Source:HGNC Symbol;Acc:HGNC:14217]"}, {"versioned_ensembl_gene_id":"ENSG00000227491.1","gene_symbol":"CCNJP1","gene_name":"cyclin J pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22512]","synonyms":"CCNJP","biotype":"processed_pseudogene","ncbi_id":"100128459","summary":null,"start":56228634,"end":56229782,"strand":-1,"description":"cyclin J pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22512]"}, {"versioned_ensembl_gene_id":"ENSG00000223559.1","gene_symbol":"AC073136.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56288230,"end":56291425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257310.1","gene_symbol":"AL589743.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19244962,"end":19247673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211791.2","gene_symbol":"TRAV13-2","gene_name":"T-cell receptor alpha variable 13-2 [Source:HGNC Symbol;Acc:HGNC:12109]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28670","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21918188,"end":21918756,"strand":1,"description":"T-cell receptor alpha variable 13-2 [Source:HGNC Symbol;Acc:HGNC:12109]"}, {"versioned_ensembl_gene_id":"ENSG00000147140.15","gene_symbol":"NONO","gene_name":"non-POU domain containing octamer binding [Source:HGNC Symbol;Acc:HGNC:7871]","synonyms":"PPP1R114,P54NRB,P54,NRB54,NMT55","biotype":"protein_coding","ncbi_id":"4841","summary":"This gene encodes an RNA-binding protein which plays various roles in the nucleus, including transcriptional regulation and RNA splicing. A rearrangement between this gene and the transcription factor E3 gene has been observed in papillary renal cell carcinoma. Alternatively spliced transcript variants have been described. Pseudogenes exist on Chromosomes 2 and 16. [provided by RefSeq, Feb 2009]","start":71283192,"end":71301168,"strand":1,"description":"non-POU domain containing octamer binding [Source:HGNC Symbol;Acc:HGNC:7871]"}, {"versioned_ensembl_gene_id":"ENSG00000254151.1","gene_symbol":"NIPA2P4","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421776","summary":null,"start":81617220,"end":81618560,"strand":-1,"description":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42044]"}, {"versioned_ensembl_gene_id":"ENSG00000251521.2","gene_symbol":"IMPA1P1","gene_name":"inositol monophosphatase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33956]","synonyms":"IMPA1P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"650747","summary":null,"start":81605569,"end":81631134,"strand":-1,"description":"inositol monophosphatase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33956]"}, {"versioned_ensembl_gene_id":"ENSG00000224156.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30784111,"end":30789336,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000253995.1","gene_symbol":"RPL10P18","gene_name":"ribosomal protein L10 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100630920","summary":null,"start":33540185,"end":33540493,"strand":1,"description":"ribosomal protein L10 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52349]"}, {"versioned_ensembl_gene_id":"ENSG00000240427.1","gene_symbol":"AC090255.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81627269,"end":81627617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205184.2","gene_symbol":"SLC10A5P1","gene_name":"SLC10A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48930]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631269","summary":null,"start":81634357,"end":81635662,"strand":-1,"description":"SLC10A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48930]"}, {"versioned_ensembl_gene_id":"ENSG00000282656.1","gene_symbol":"TBC1D3J","gene_name":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100510707","summary":null,"start":36450330,"end":36457907,"strand":-1,"description":"TBC1 domain family member 3J [Source:HGNC Symbol;Acc:HGNC:51247]"}, {"versioned_ensembl_gene_id":"ENSG00000173451.6","gene_symbol":"THAP2","gene_name":"THAP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20854]","synonyms":"DKFZP564I0422","biotype":"protein_coding","ncbi_id":"83591","summary":null,"start":71663009,"end":71680639,"strand":1,"description":"THAP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20854]"}, {"versioned_ensembl_gene_id":"ENSG00000197891.11","gene_symbol":"SLC22A12","gene_name":"solute carrier family 22 member 12 [Source:HGNC Symbol;Acc:HGNC:17989]","synonyms":"URAT1,RST,OAT4L","biotype":"protein_coding","ncbi_id":"116085","summary":"The protein encoded by this gene is a member of the organic anion transporter (OAT) family, and it acts as a urate transporter to regulate urate levels in blood. This protein is an integral membrane protein primarily found in epithelial cells of the proximal tubule of the kidney. An elevated level of serum urate, hyperuricemia, is associated with increased incidences of gout, and mutations in this gene cause renal hypouricemia type 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":64590641,"end":64602353,"strand":1,"description":"solute carrier family 22 member 12 [Source:HGNC Symbol;Acc:HGNC:17989]"}, {"versioned_ensembl_gene_id":"ENSG00000133874.1","gene_symbol":"RNF122","gene_name":"ring finger protein 122 [Source:HGNC Symbol;Acc:HGNC:21147]","synonyms":"FLJ12526","biotype":"protein_coding","ncbi_id":"79845","summary":"The encoded protein contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. The encoded protein is localized to the endoplasmic reticulum and golgi apparatus, and may be associated with cell viability. [provided by RefSeq, Jul 2013]","start":33547755,"end":33567125,"strand":-1,"description":"ring finger protein 122 [Source:HGNC Symbol;Acc:HGNC:21147]"}, {"versioned_ensembl_gene_id":"ENSG00000205634.6","gene_symbol":"LINC00898","gene_name":"long intergenic non-protein coding RNA 898 [Source:HGNC Symbol;Acc:HGNC:48581]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400932","summary":null,"start":47621043,"end":47631569,"strand":-1,"description":"long intergenic non-protein coding RNA 898 [Source:HGNC Symbol;Acc:HGNC:48581]"}, {"versioned_ensembl_gene_id":"ENSG00000172081.13","gene_symbol":"MOB3A","gene_name":"MOB kinase activator 3A [Source:HGNC Symbol;Acc:HGNC:29802]","synonyms":"moblak,MOBKL2A,MOB1C,MOB-LAK","biotype":"protein_coding","ncbi_id":"126308","summary":null,"start":2071038,"end":2096673,"strand":-1,"description":"MOB kinase activator 3A [Source:HGNC Symbol;Acc:HGNC:29802]"}, {"versioned_ensembl_gene_id":"ENSG00000242339.1","gene_symbol":"LINC02025","gene_name":"long intergenic non-protein coding RNA 2025 [Source:HGNC Symbol;Acc:HGNC:52860]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377192","summary":null,"start":84884936,"end":84893379,"strand":1,"description":"long intergenic non-protein coding RNA 2025 [Source:HGNC Symbol;Acc:HGNC:52860]"}, {"versioned_ensembl_gene_id":"ENSG00000213468.5","gene_symbol":"FIRRE","gene_name":"firre intergenic repeating RNA element [Source:HGNC Symbol;Acc:HGNC:49627]","synonyms":"LINC01200","biotype":"lincRNA","ncbi_id":"286467","summary":"This gene produces a long RNA containing a repeating sequence. This RNA interacts with heterogeneous nuclear ribonucleoprotein U and coats chromosomes, where it plays an important role in the maintenance of repressive chromatin. This transcript can also act post-transcriptionally to regulate the stability of mRNAs during the innate immune response. [provided by RefSeq, Dec 2017]","start":131691530,"end":131830643,"strand":-1,"description":"firre intergenic repeating RNA element [Source:HGNC Symbol;Acc:HGNC:49627]"}, {"versioned_ensembl_gene_id":"ENSG00000273136.6","gene_symbol":"NBPF26","gene_name":"NBPF member 26 [Source:HGNC Symbol;Acc:HGNC:49571]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060684","summary":null,"start":120723923,"end":120841481,"strand":1,"description":"NBPF member 26 [Source:HGNC Symbol;Acc:HGNC:49571]"}, {"versioned_ensembl_gene_id":"ENSG00000219491.6","gene_symbol":"TPT1P8","gene_name":"tumor protein, translationally-controlled 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:24088]","synonyms":"FKSG2","biotype":"unprocessed_pseudogene","ncbi_id":"59347","summary":null,"start":36888482,"end":36889307,"strand":1,"description":"tumor protein, translationally-controlled 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:24088]"}, {"versioned_ensembl_gene_id":"ENSG00000179922.5","gene_symbol":"ZNF784","gene_name":"zinc finger protein 784 [Source:HGNC Symbol;Acc:HGNC:33111]","synonyms":"MGC75238","biotype":"protein_coding","ncbi_id":"147808","summary":null,"start":55620742,"end":55624601,"strand":-1,"description":"zinc finger protein 784 [Source:HGNC Symbol;Acc:HGNC:33111]"}, {"versioned_ensembl_gene_id":"ENSG00000219545.11","gene_symbol":"UMAD1","gene_name":"UBAP1-MVB12-associated (UMA) domain containing 1 [Source:HGNC Symbol;Acc:HGNC:48955]","synonyms":"RPA3OS,RPA3-AS1","biotype":"protein_coding","ncbi_id":"729852","summary":null,"start":7640711,"end":7968020,"strand":1,"description":"UBAP1-MVB12-associated (UMA) domain containing 1 [Source:HGNC Symbol;Acc:HGNC:48955]"}, {"versioned_ensembl_gene_id":"ENSG00000154655.15","gene_symbol":"L3MBTL4","gene_name":"L3MBTL4, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:26677]","synonyms":"HsT1031,FLJ35936","biotype":"protein_coding","ncbi_id":"91133","summary":null,"start":5954706,"end":6415237,"strand":-1,"description":"L3MBTL4, histone methyl-lysine binding protein [Source:HGNC Symbol;Acc:HGNC:26677]"}, {"versioned_ensembl_gene_id":"ENSG00000282551.1","gene_symbol":"AC024940.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31313890,"end":31314302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215262.7","gene_symbol":"KCNU1","gene_name":"potassium calcium-activated channel subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:18867]","synonyms":"Slo3,KCNMC1,Kcnma3,KCa5.1","biotype":"protein_coding","ncbi_id":"157855","summary":"This gene encodes a member of the potassium channel family of proteins. The encoded voltage-gated ion channel allows the outward flow of potassium ions during plasma membrane hyperpolarization in sperm. Opening of this channel may be regulated by calcium ion levels. Homozygous knockout mice that lack the related mouse gene exhibit male sterility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":36784324,"end":36936128,"strand":1,"description":"potassium calcium-activated channel subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:18867]"}, {"versioned_ensembl_gene_id":"ENSG00000235307.9","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"FSRG1,NAT,D6S113E,KIAA9001,RING3,BRD2-IT1","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":33059372,"end":33122227,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000203778.7","gene_symbol":"FAM229B","gene_name":"family with sequence similarity 229 member B [Source:HGNC Symbol;Acc:HGNC:33858]","synonyms":"DKFZp586F0922,C6orf225,LOC619208","biotype":"protein_coding","ncbi_id":"619208","summary":null,"start":112087599,"end":112102790,"strand":1,"description":"family with sequence similarity 229 member B [Source:HGNC Symbol;Acc:HGNC:33858]"}, {"versioned_ensembl_gene_id":"ENSG00000260460.1","gene_symbol":"AL365181.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156509854,"end":156511681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241741.1","gene_symbol":"RPL7AP30","gene_name":"ribosomal protein L7a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35757]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441034","summary":null,"start":112788083,"end":112788878,"strand":-1,"description":"ribosomal protein L7a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35757]"}, {"versioned_ensembl_gene_id":"ENSG00000269985.1","gene_symbol":"AL021328.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5451683,"end":5458075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223804.5","gene_symbol":"AC244669.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":120267334,"end":120341871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254233.1","gene_symbol":"LINC02365","gene_name":"long intergenic non-protein coding RNA 2365 [Source:HGNC Symbol;Acc:HGNC:53285]","synonyms":"LVCAT8","biotype":"lincRNA","ncbi_id":"105377586","summary":null,"start":184584093,"end":184625030,"strand":-1,"description":"long intergenic non-protein coding RNA 2365 [Source:HGNC Symbol;Acc:HGNC:53285]"}, {"versioned_ensembl_gene_id":"ENSG00000249056.1","gene_symbol":"AC099343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":184559175,"end":184559783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189045.13","gene_symbol":"ANKDD1B","gene_name":"ankyrin repeat and death domain containing 1B [Source:HGNC Symbol;Acc:HGNC:32525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728780","summary":null,"start":75611459,"end":75671846,"strand":1,"description":"ankyrin repeat and death domain containing 1B [Source:HGNC Symbol;Acc:HGNC:32525]"}, {"versioned_ensembl_gene_id":"ENSG00000113575.9","gene_symbol":"PPP2CA","gene_name":"protein phosphatase 2 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9299]","synonyms":"PP2AC,PP2Calpha","biotype":"protein_coding","ncbi_id":"5515","summary":"This gene encodes the phosphatase 2A catalytic subunit. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. This gene encodes an alpha isoform of the catalytic subunit. [provided by RefSeq, Jul 2008]","start":134194334,"end":134226142,"strand":-1,"description":"protein phosphatase 2 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9299]"}, {"versioned_ensembl_gene_id":"ENSG00000150594.6","gene_symbol":"ADRA2A","gene_name":"adrenoceptor alpha 2A [Source:HGNC Symbol;Acc:HGNC:281]","synonyms":"ADRAR,ADRA2R,ADRA2","biotype":"protein_coding","ncbi_id":"150","summary":"Alpha-2-adrenergic receptors are members of the G protein-coupled receptor superfamily. The alpha-2-adrenergic receptors are a type of adrenergic receptors (for adrenaline or epinephrine), which inhibit adenylate cyclase. These receptors include 3 highly homologous subtypes: alpha2A, alpha2B, and alpha2C. They are involved in regulating the release of neurotransmitter molecules from sympathetic nerves and from adrenergic neurons in the central nervous system. The sympathetic nervous system regulates cardiovascular function by activating adrenergic receptors in the heart, blood vessels and kidney. Studies in mouse revealed that both the alpha2A and alpha2C receptor subtypes were required for presynaptic transmitter release from the sympathetic nervous system in the heart and from central noradrenergic neurons. The alpha-2-adrenergic receptors are also involved in catecholamine signaling by extracellular regulated protein kinase 1 and 2 (ERK1/2) pathways. A clear association between the alpha-2-adrenergic receptor and disease has not been yet established. [provided by RefSeq, Sep 2019]","start":111077163,"end":111080907,"strand":1,"description":"adrenoceptor alpha 2A [Source:HGNC Symbol;Acc:HGNC:281]"}, {"versioned_ensembl_gene_id":"ENSG00000145982.11","gene_symbol":"FARS2","gene_name":"phenylalanyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21062]","synonyms":"FARS1,dJ236A3.1","biotype":"protein_coding","ncbi_id":"10667","summary":"This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":5261044,"end":5771580,"strand":1,"description":"phenylalanyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21062]"}, {"versioned_ensembl_gene_id":"ENSG00000125817.7","gene_symbol":"CENPB","gene_name":"centromere protein B [Source:HGNC Symbol;Acc:HGNC:1852]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1059","summary":"This gene product is a highly conserved protein that facilitates centromere formation. It is a DNA-binding protein that is derived from transposases of the pogo DNA transposon family. It contains a helix-loop-helix DNA binding motif at the N-terminus, and a dimerization domain at the C-terminus. The DNA binding domain recognizes and binds a 17-bp sequence (CENP-B box) in the centromeric alpha satellite DNA. This protein is proposed to play an important role in the assembly of specific centromere structures in interphase nuclei and on mitotic chromosomes. It is also considered a major centromere autoantigen recognized by sera from patients with anti-centromere antibodies. [provided by RefSeq, Jul 2008]","start":3783851,"end":3786690,"strand":-1,"description":"centromere protein B [Source:HGNC Symbol;Acc:HGNC:1852]"}, {"versioned_ensembl_gene_id":"ENSG00000148690.11","gene_symbol":"FRA10AC1","gene_name":"FRA10A associated CGG repeat 1 [Source:HGNC Symbol;Acc:HGNC:1162]","synonyms":"C10orf4","biotype":"protein_coding","ncbi_id":"118924","summary":"The protein encoded by this gene is a nuclear phosphoprotein of unknown function. This gene contains a tandem CGG repeat region within a CpG island that normally consists of 8-14 repeats but can expand to over 200 repeats. The repeat region is within the 5' UTR of some transcript variants, but is intronic to another variant. The expanded repeat allele is a fragile site and becomes hypermethylated, causing a reduction in gene expression. A disease phenotype has not been associated with expanded alleles. This gene is found within the rare FRA10A folate-sensitive fragile site. [provided by RefSeq, Dec 2016]","start":93667883,"end":93702572,"strand":-1,"description":"FRA10A associated CGG repeat 1 [Source:HGNC Symbol;Acc:HGNC:1162]"}, {"versioned_ensembl_gene_id":"ENSG00000253748.2","gene_symbol":"CYP4F44P","gene_name":"cytochrome P450 family 4 subfamily F member 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:39957]","synonyms":"CYP4F-se12[6:8]","biotype":"unprocessed_pseudogene","ncbi_id":"106480733","summary":null,"start":43539973,"end":43540927,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:39957]"}, {"versioned_ensembl_gene_id":"ENSG00000229413.2","gene_symbol":"AC018638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128653690,"end":128654019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274556.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724447,"end":54736132,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000177511.5","gene_symbol":"ST8SIA3","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:14269]","synonyms":"SIAT8C","biotype":"protein_coding","ncbi_id":"51046","summary":"ST8SIA3 belongs to a family of sialyltransferases that form sialyl-alpha-2,8-sialyl-R linkages at the nonreducing termini of glycoconjugates (Lee et al., 1998 [PubMed 9826427]).[supplied by OMIM, Mar 2008]","start":57350813,"end":57371731,"strand":1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:14269]"}, {"versioned_ensembl_gene_id":"ENSG00000251489.2","gene_symbol":"AC108941.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69888877,"end":69889406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152154.10","gene_symbol":"TMEM178A","gene_name":"transmembrane protein 178A [Source:HGNC Symbol;Acc:HGNC:28517]","synonyms":"TMEM178,MGC33926","biotype":"protein_coding","ncbi_id":"130733","summary":null,"start":39664982,"end":39717963,"strand":1,"description":"transmembrane protein 178A [Source:HGNC Symbol;Acc:HGNC:28517]"}, {"versioned_ensembl_gene_id":"ENSG00000183628.12","gene_symbol":"DGCR6","gene_name":"DiGeorge syndrome critical region gene 6 [Source:HGNC Symbol;Acc:HGNC:2846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8214","summary":"DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. The product of this gene shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the gamma-1 subunit of human laminin. This gene is a candidate for involvement in DiGeorge syndrome pathology and in schizophrenia. [provided by RefSeq, Nov 2008]","start":18906028,"end":18914238,"strand":1,"description":"DiGeorge syndrome critical region gene 6 [Source:HGNC Symbol;Acc:HGNC:2846]"}, {"versioned_ensembl_gene_id":"ENSG00000224109.2","gene_symbol":"CENPVL3","gene_name":"centromere protein V like 3 [Source:HGNC Symbol;Acc:HGNC:43880]","synonyms":"CENPVP3","biotype":"protein_coding","ncbi_id":"347549","summary":null,"start":51618055,"end":51618918,"strand":-1,"description":"centromere protein V like 3 [Source:HGNC Symbol;Acc:HGNC:43880]"}, {"versioned_ensembl_gene_id":"ENSG00000144229.11","gene_symbol":"THSD7B","gene_name":"thrombospondin type 1 domain containing 7B [Source:HGNC Symbol;Acc:HGNC:29348]","synonyms":"KIAA1679","biotype":"protein_coding","ncbi_id":"80731","summary":null,"start":136765545,"end":137677717,"strand":1,"description":"thrombospondin type 1 domain containing 7B [Source:HGNC Symbol;Acc:HGNC:29348]"}, {"versioned_ensembl_gene_id":"ENSG00000280611.1","gene_symbol":"AC128709.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":197445061,"end":197458322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236605.1","gene_symbol":"AC023115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67324627,"end":67325304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240601.1","gene_symbol":"RPL9P15","gene_name":"ribosomal protein L9 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270857","summary":null,"start":154676588,"end":154677119,"strand":-1,"description":"ribosomal protein L9 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35539]"}, {"versioned_ensembl_gene_id":"ENSG00000215241.3","gene_symbol":"LINC02449","gene_name":"long intergenic non-protein coding RNA 2449 [Source:HGNC Symbol;Acc:HGNC:53381]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927905","summary":null,"start":8235415,"end":8242564,"strand":1,"description":"long intergenic non-protein coding RNA 2449 [Source:HGNC Symbol;Acc:HGNC:53381]"}, {"versioned_ensembl_gene_id":"ENSG00000250550.3","gene_symbol":"PPBPP1","gene_name":"pro-platelet basic protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9241]","synonyms":"PPBPL1,TGB2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"728045","summary":null,"start":73847866,"end":73848829,"strand":1,"description":"pro-platelet basic protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9241]"}, {"versioned_ensembl_gene_id":"ENSG00000231873.1","gene_symbol":"AC099560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40766207,"end":40862626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279025.1","gene_symbol":"AL356863.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":38372856,"end":38373935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171847.10","gene_symbol":"FAM90A1","gene_name":"family with sequence similarity 90 member A1 [Source:HGNC Symbol;Acc:HGNC:25526]","synonyms":"FLJ10408","biotype":"protein_coding","ncbi_id":"55138","summary":"FAM90A1 belongs to subfamily I of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]).[supplied by OMIM, Oct 2009]","start":8221260,"end":8227618,"strand":-1,"description":"family with sequence similarity 90 member A1 [Source:HGNC Symbol;Acc:HGNC:25526]"}, {"versioned_ensembl_gene_id":"ENSG00000160214.12","gene_symbol":"RRP1","gene_name":"ribosomal RNA processing 1 [Source:HGNC Symbol;Acc:HGNC:18785]","synonyms":"RRP1A,Nop52,NNP-1,D21S2056E","biotype":"protein_coding","ncbi_id":"8568","summary":"The protein encoded by this gene is the putative homolog of the yeast ribosomal RNA processing protein RRP1. The encoded protein is involved in the late stages of nucleologenesis at the end of mitosis, and may be required for the generation of 28S rRNA. [provided by RefSeq, Jul 2008]","start":43789513,"end":43805293,"strand":1,"description":"ribosomal RNA processing 1 [Source:HGNC Symbol;Acc:HGNC:18785]"}, {"versioned_ensembl_gene_id":"ENSG00000167930.15","gene_symbol":"FAM234A","gene_name":"family with sequence similarity 234 member A [Source:HGNC Symbol;Acc:HGNC:14163]","synonyms":"ITFG3,FLJ32603,DKFZP761D0211,C16orf9","biotype":"protein_coding","ncbi_id":"83986","summary":null,"start":234546,"end":268971,"strand":1,"description":"family with sequence similarity 234 member A [Source:HGNC Symbol;Acc:HGNC:14163]"}, {"versioned_ensembl_gene_id":"ENSG00000275331.5","gene_symbol":"ABCC6","gene_name":"ATP binding cassette subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:57]","synonyms":"PXE,MRP6,MLP1,EST349056,ARA,URG7","biotype":"protein_coding","ncbi_id":"368","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). The encoded protein, a member of the MRP subfamily, is involved in multi-drug resistance. Mutations in this gene cause pseudoxanthoma elasticum. Alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Jul 2008]","start":16233991,"end":16308660,"strand":-1,"description":"ATP binding cassette subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:57]"}, {"versioned_ensembl_gene_id":"ENSG00000162913.9","gene_symbol":"OBSCN-AS1","gene_name":"OBSCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32047]","synonyms":"FLJ31994,C1orf145","biotype":"protein_coding","ncbi_id":"574407","summary":null,"start":228203506,"end":228213664,"strand":-1,"description":"OBSCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:32047]"}, {"versioned_ensembl_gene_id":"ENSG00000238185.1","gene_symbol":"AL353680.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30973289,"end":30977623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176571.11","gene_symbol":"CNBD1","gene_name":"cyclic nucleotide binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26663]","synonyms":"FLJ35802","biotype":"protein_coding","ncbi_id":"168975","summary":null,"start":86866442,"end":87615219,"strand":1,"description":"cyclic nucleotide binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26663]"}, {"versioned_ensembl_gene_id":"ENSG00000258355.1","gene_symbol":"AC079174.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":106245613,"end":106246956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226479.3","gene_symbol":"TMEM185B","gene_name":"transmembrane protein 185B [Source:HGNC Symbol;Acc:HGNC:18896]","synonyms":"FLJ20979,FAM11B","biotype":"protein_coding","ncbi_id":"79134","summary":null,"start":120221278,"end":120223408,"strand":-1,"description":"transmembrane protein 185B [Source:HGNC Symbol;Acc:HGNC:18896]"}, {"versioned_ensembl_gene_id":"ENSG00000134249.6","gene_symbol":"ADAM30","gene_name":"ADAM metallopeptidase domain 30 [Source:HGNC Symbol;Acc:HGNC:208]","synonyms":"svph4","biotype":"protein_coding","ncbi_id":"11085","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This gene is testis-specific and contains a polymorphic region, resulting in isoforms with varying numbers of C-terminal repeats. [provided by RefSeq, Jul 2008]","start":119893533,"end":119896495,"strand":-1,"description":"ADAM metallopeptidase domain 30 [Source:HGNC Symbol;Acc:HGNC:208]"}, {"versioned_ensembl_gene_id":"ENSG00000132256.18","gene_symbol":"TRIM5","gene_name":"tripartite motif containing 5 [Source:HGNC Symbol;Acc:HGNC:16276]","synonyms":"TRIM5alpha,RNF88","biotype":"protein_coding","ncbi_id":"85363","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein forms homo-oligomers via the coilel-coil region and localizes to cytoplasmic bodies. It appears to function as a E3 ubiquitin-ligase and ubiqutinates itself to regulate its subcellular localization. It may play a role in retroviral restriction. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Dec 2009]","start":5663557,"end":5938619,"strand":-1,"description":"tripartite motif containing 5 [Source:HGNC Symbol;Acc:HGNC:16276]"}, {"versioned_ensembl_gene_id":"ENSG00000260019.1","gene_symbol":"LINC01992","gene_name":"long intergenic non-protein coding RNA 1992 [Source:HGNC Symbol;Acc:HGNC:52824]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371708","summary":null,"start":27929548,"end":27974223,"strand":-1,"description":"long intergenic non-protein coding RNA 1992 [Source:HGNC Symbol;Acc:HGNC:52824]"}, {"versioned_ensembl_gene_id":"ENSG00000279940.1","gene_symbol":"AC073862.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130956384,"end":130958031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166046.10","gene_symbol":"TCP11L2","gene_name":"t-complex 11 like 2 [Source:HGNC Symbol;Acc:HGNC:28627]","synonyms":"MGC40368","biotype":"protein_coding","ncbi_id":"255394","summary":null,"start":106301929,"end":106347015,"strand":1,"description":"t-complex 11 like 2 [Source:HGNC Symbol;Acc:HGNC:28627]"}, {"versioned_ensembl_gene_id":"ENSG00000237624.1","gene_symbol":"OXCT2P1","gene_name":"3-oxoacid CoA-transferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21627]","synonyms":"OXCT2P","biotype":"unprocessed_pseudogene","ncbi_id":"192217","summary":null,"start":39514956,"end":39516490,"strand":1,"description":"3-oxoacid CoA-transferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21627]"}, {"versioned_ensembl_gene_id":"ENSG00000256863.1","gene_symbol":"AP001880.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63237957,"end":63239114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236108.1","gene_symbol":"AC093422.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205134646,"end":205134950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282687.1","gene_symbol":"IGHVIII-22-2","gene_name":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]","synonyms":"IGHV(III)-22-2","biotype":"IG_V_pseudogene","ncbi_id":"28349","summary":null,"start":106265459,"end":106265486,"strand":-1,"description":"immunoglobulin heavy variable (III)-22-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5696]"}, {"versioned_ensembl_gene_id":"ENSG00000253778.1","gene_symbol":"AC090572.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86765935,"end":86818558,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282609.1","gene_symbol":"IGHV3-22","gene_name":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28443","summary":null,"start":106258533,"end":106258994,"strand":-1,"description":"immunoglobulin heavy variable 3-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5587]"}, {"versioned_ensembl_gene_id":"ENSG00000270625.1","gene_symbol":"AC004835.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119222564,"end":119223245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231001.2","gene_symbol":"CCNB1IP1P3","gene_name":"cyclin B1 interacting protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128456","summary":null,"start":94776739,"end":94777567,"strand":-1,"description":"cyclin B1 interacting protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37695]"}, {"versioned_ensembl_gene_id":"ENSG00000197658.9","gene_symbol":"SLC22A24","gene_name":"solute carrier family 22 member 24 [Source:HGNC Symbol;Acc:HGNC:28542]","synonyms":"NET46,MGC34821","biotype":"protein_coding","ncbi_id":"283238","summary":"SLC22A24 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]","start":63079940,"end":63144221,"strand":-1,"description":"solute carrier family 22 member 24 [Source:HGNC Symbol;Acc:HGNC:28542]"}, {"versioned_ensembl_gene_id":"ENSG00000230170.1","gene_symbol":"HNRNPA1P28","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39546]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288038","summary":null,"start":119220782,"end":119221742,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:39546]"}, {"versioned_ensembl_gene_id":"ENSG00000183615.5","gene_symbol":"FAM167B","gene_name":"family with sequence similarity 167 member B [Source:HGNC Symbol;Acc:HGNC:28133]","synonyms":"MGC10820,C1orf90","biotype":"protein_coding","ncbi_id":"84734","summary":null,"start":32247233,"end":32248856,"strand":1,"description":"family with sequence similarity 167 member B [Source:HGNC Symbol;Acc:HGNC:28133]"}, {"versioned_ensembl_gene_id":"ENSG00000228557.1","gene_symbol":"HSPA8P17","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:44932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533658","summary":null,"start":30988085,"end":30990572,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:44932]"}, {"versioned_ensembl_gene_id":"ENSG00000278385.1","gene_symbol":"AC121338.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47905122,"end":47906865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067606.16","gene_symbol":"PRKCZ","gene_name":"protein kinase C zeta [Source:HGNC Symbol;Acc:HGNC:9412]","synonyms":"PKC2","biotype":"protein_coding","ncbi_id":"5590","summary":"Protein kinase C (PKC) zeta is a member of the PKC family of serine/threonine kinases which are involved in a variety of cellular processes such as proliferation, differentiation and secretion. Unlike the classical PKC isoenzymes which are calcium-dependent, PKC zeta exhibits a kinase activity which is independent of calcium and diacylglycerol but not of phosphatidylserine. Furthermore, it is insensitive to typical PKC inhibitors and cannot be activated by phorbol ester. Unlike the classical PKC isoenzymes, it has only a single zinc finger module. These structural and biochemical properties indicate that the zeta subspecies is related to, but distinct from other isoenzymes of PKC. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":2050470,"end":2185395,"strand":1,"description":"protein kinase C zeta [Source:HGNC Symbol;Acc:HGNC:9412]"}, {"versioned_ensembl_gene_id":"ENSG00000234130.2","gene_symbol":"AL359263.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93222220,"end":93225015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258118.1","gene_symbol":"AC010198.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30861921,"end":30862179,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225976.5","gene_symbol":"CKS1BP2","gene_name":"CDC28 protein kinase regulatory subunit 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24232]","synonyms":"bA192N10.2","biotype":"processed_pseudogene","ncbi_id":"246714","summary":null,"start":29697935,"end":29698174,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24232]"}, {"versioned_ensembl_gene_id":"ENSG00000141905.18","gene_symbol":"NFIC","gene_name":"nuclear factor I C [Source:HGNC Symbol;Acc:HGNC:7786]","synonyms":"CTF,NFI,NF-I,CTF5","biotype":"protein_coding","ncbi_id":"4782","summary":"The protein encoded by this gene belongs to the CTF/NF-I family. These are dimeric DNA-binding proteins, and function as cellular transcription factors and as replication factors for adenovirus DNA replication. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":3314403,"end":3469217,"strand":1,"description":"nuclear factor I C [Source:HGNC Symbol;Acc:HGNC:7786]"}, {"versioned_ensembl_gene_id":"ENSG00000279599.1","gene_symbol":"AC005514.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3371395,"end":3371602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149089.12","gene_symbol":"APIP","gene_name":"APAF1 interacting protein [Source:HGNC Symbol;Acc:HGNC:17581]","synonyms":"Mmrp19,CGI-29,APIP2","biotype":"protein_coding","ncbi_id":"51074","summary":"APIP is an APAF1 (MIM 602233)-interacting protein that acts as a negative regulator of ischemic/hypoxic injury (Cho et al., 2004 [PubMed 15262985]).[supplied by OMIM, Dec 2008]","start":34853094,"end":34916499,"strand":-1,"description":"APAF1 interacting protein [Source:HGNC Symbol;Acc:HGNC:17581]"}, {"versioned_ensembl_gene_id":"ENSG00000278646.1","gene_symbol":"AC008162.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":120877496,"end":120878924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278786.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786474,"end":54798295,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000261647.1","gene_symbol":"IMPDH1P11","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6054]","synonyms":"IMPDHL1","biotype":"processed_pseudogene","ncbi_id":"727833","summary":null,"start":10111382,"end":10112885,"strand":1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6054]"}, {"versioned_ensembl_gene_id":"ENSG00000261810.1","gene_symbol":"AC133565.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10033684,"end":10037297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271041.1","gene_symbol":"AL670379.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120947483,"end":120947735,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277215.1","gene_symbol":"SPANXA2-OT1","gene_name":"SPANXA2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:31683]","synonyms":"FLJ36186,CXorf18","biotype":"lincRNA","ncbi_id":"619455","summary":null,"start":141502849,"end":141649927,"strand":1,"description":"SPANXA2 overlapping transcript 1 [Source:HGNC Symbol;Acc:HGNC:31683]"}, {"versioned_ensembl_gene_id":"ENSG00000234688.1","gene_symbol":"AL049749.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36703918,"end":36721472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271978.1","gene_symbol":"AL359643.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5031756,"end":5054423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007171.16","gene_symbol":"NOS2","gene_name":"nitric oxide synthase 2 [Source:HGNC Symbol;Acc:HGNC:7873]","synonyms":"NOS,iNOS,HEP-NOS,NOS2A","biotype":"protein_coding","ncbi_id":"4843","summary":"Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase which is expressed in liver and is inducible by a combination of lipopolysaccharide and certain cytokines. Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":27756766,"end":27800499,"strand":-1,"description":"nitric oxide synthase 2 [Source:HGNC Symbol;Acc:HGNC:7873]"}, {"versioned_ensembl_gene_id":"ENSG00000257859.1","gene_symbol":"CASC18","gene_name":"cancer susceptibility 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49463]","synonyms":"LOC101929110","biotype":"lincRNA","ncbi_id":"101929110","summary":null,"start":105704203,"end":105744062,"strand":1,"description":"cancer susceptibility 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49463]"}, {"versioned_ensembl_gene_id":"ENSG00000266202.1","gene_symbol":"AC005697.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":27798806,"end":27893365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213882.2","gene_symbol":"CYB5AP4","gene_name":"cytochrome b5 type A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:2575]","synonyms":"Psgb-5-2,CYB5P4,bA189G24.1","biotype":"processed_pseudogene","ncbi_id":"1532","summary":null,"start":22885670,"end":22886068,"strand":-1,"description":"cytochrome b5 type A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:2575]"}, {"versioned_ensembl_gene_id":"ENSG00000214093.3","gene_symbol":"AL096701.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31559483,"end":31559939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233962.1","gene_symbol":"AC064862.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57652736,"end":57653459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236261.1","gene_symbol":"AC064862.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57652875,"end":57653208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231953.2","gene_symbol":"AL031432.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25208139,"end":25209437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226444.2","gene_symbol":"ACTR3BP6","gene_name":"ACTR3B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38683]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644773","summary":null,"start":11124337,"end":11125705,"strand":1,"description":"ACTR3B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:38683]"}, {"versioned_ensembl_gene_id":"ENSG00000242613.1","gene_symbol":"AC063952.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120388029,"end":120389315,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236712.1","gene_symbol":"AC079448.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7293508,"end":7293880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279169.2","gene_symbol":"PRAMEF13","gene_name":"PRAME family member 13 [Source:HGNC Symbol;Acc:HGNC:13262]","synonyms":"OTTHUMG00000008034","biotype":"protein_coding","ncbi_id":"400736","summary":null,"start":13196330,"end":13201409,"strand":-1,"description":"PRAME family member 13 [Source:HGNC Symbol;Acc:HGNC:13262]"}, {"versioned_ensembl_gene_id":"ENSG00000263508.5","gene_symbol":"AC015908.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10849541,"end":10880895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231355.1","gene_symbol":"AP000302.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33482499,"end":33484258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234457.1","gene_symbol":"AC006960.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36305631,"end":36305904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226302.1","gene_symbol":"AC122683.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40603125,"end":40605427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239659.2","gene_symbol":"AC104971.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58631259,"end":58632120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270957.1","gene_symbol":"AC092175.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57485166,"end":57485895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165091.15","gene_symbol":"TMC1","gene_name":"transmembrane channel like 1 [Source:HGNC Symbol;Acc:HGNC:16513]","synonyms":"DFNB7,DFNB11,DFNA36","biotype":"protein_coding","ncbi_id":"117531","summary":"This gene is considered a member of a gene family predicted to encode transmembrane proteins. The specific function of this gene is unknown; however, it is known to be required for normal function of cochlear hair cells. Mutations in this gene have been associated with progressive postlingual hearing loss and profound prelingual deafness. [provided by RefSeq, Jul 2008]","start":72521801,"end":72836351,"strand":1,"description":"transmembrane channel like 1 [Source:HGNC Symbol;Acc:HGNC:16513]"}, {"versioned_ensembl_gene_id":"ENSG00000250711.1","gene_symbol":"PRELID3BP7","gene_name":"PRELI domain containing 3B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49069]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730974","summary":null,"start":42972624,"end":42973092,"strand":1,"description":"PRELI domain containing 3B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49069]"}, {"versioned_ensembl_gene_id":"ENSG00000239862.1","gene_symbol":"IGKV1-37","gene_name":"immunoglobulin kappa variable 1-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5739]","synonyms":"O14,IGKV137","biotype":"IG_V_gene","ncbi_id":"28931","summary":null,"start":89297264,"end":89297785,"strand":-1,"description":"immunoglobulin kappa variable 1-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5739]"}, {"versioned_ensembl_gene_id":"ENSG00000266786.1","gene_symbol":"LGALS9DP","gene_name":"galectin 9D, pseudogene [Source:HGNC Symbol;Acc:HGNC:49896]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"645754","summary":null,"start":27746132,"end":27754954,"strand":1,"description":"galectin 9D, pseudogene [Source:HGNC Symbol;Acc:HGNC:49896]"}, {"versioned_ensembl_gene_id":"ENSG00000165240.18","gene_symbol":"ATP7A","gene_name":"ATPase copper transporting alpha [Source:HGNC Symbol;Acc:HGNC:869]","synonyms":"MNK","biotype":"protein_coding","ncbi_id":"538","summary":"This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed. [provided by RefSeq, Aug 2013]","start":77910656,"end":78050395,"strand":1,"description":"ATPase copper transporting alpha [Source:HGNC Symbol;Acc:HGNC:869]"}, {"versioned_ensembl_gene_id":"ENSG00000146197.8","gene_symbol":"SCUBE3","gene_name":"signal peptide, CUB domain and EGF like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:13655]","synonyms":"FLJ34743,CEGF3","biotype":"protein_coding","ncbi_id":"222663","summary":"This gene encodes a member of the signal peptide, complement subcomponents C1r/C1s, Uegf, bone morphogenetic protein-1 and epidermal growth factor-like domain containing protein family. Overexpression of this gene in human embryonic kidney cells results in secretion of a glycosylated form of the protein that forms oligomers and tethers to the cell surface. This gene is upregulated in lung cancer tumor tissue compared to healthy tissue and is associated with loss of the epithelial marker E-cadherin and with increased expression of vimentin, a mesenchymal marker. In addition, the protein encoded by this gene is a transforming growth factor beta receptor ligand, and when secreted by cancer cells, it can be cleaved in vitro to release the N-terminal epidermal growth factor-like repeat domain and the C-terminal complement subcomponents C1r/C1s domain. Both the full length protein and C-terminal fragment can bind to the transforming growth factor beta type II receptor to promote the epithelial-mesenchymal transition and tumor angiogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":35214419,"end":35253079,"strand":1,"description":"signal peptide, CUB domain and EGF like domain containing 3 [Source:HGNC Symbol;Acc:HGNC:13655]"}, {"versioned_ensembl_gene_id":"ENSG00000280267.4","gene_symbol":"PRAMEF26","gene_name":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645359","summary":null,"start":13148905,"end":13155961,"strand":-1,"description":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]"}, {"versioned_ensembl_gene_id":"ENSG00000109193.11","gene_symbol":"SULT1E1","gene_name":"sulfotransferase family 1E member 1 [Source:HGNC Symbol;Acc:HGNC:11377]","synonyms":"STE,EST","biotype":"protein_coding","ncbi_id":"6783","summary":"Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that transfers a sulfo moiety to and from estrone, which may control levels of estrogen receptors. [provided by RefSeq, Jul 2008]","start":69841212,"end":69860152,"strand":-1,"description":"sulfotransferase family 1E member 1 [Source:HGNC Symbol;Acc:HGNC:11377]"}, {"versioned_ensembl_gene_id":"ENSG00000231270.1","gene_symbol":"AL772284.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118938153,"end":118939134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227100.1","gene_symbol":"AL773535.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30348767,"end":30349400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235824.4","gene_symbol":"LINC00837","gene_name":"long intergenic non-protein coding RNA 837 [Source:HGNC Symbol;Acc:HGNC:27436]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507605","summary":null,"start":28789188,"end":28796113,"strand":-1,"description":"long intergenic non-protein coding RNA 837 [Source:HGNC Symbol;Acc:HGNC:27436]"}, {"versioned_ensembl_gene_id":"ENSG00000249002.2","gene_symbol":"AC096745.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119006032,"end":119006401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278419.1","gene_symbol":"AL451164.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3134566,"end":3145166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206458.10","gene_symbol":"PSORS1C1","gene_name":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]","synonyms":"C6orf16,SEEK1","biotype":"protein_coding","ncbi_id":"170679","summary":"This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]","start":31107156,"end":31132470,"strand":1,"description":"psoriasis susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:17202]"}, {"versioned_ensembl_gene_id":"ENSG00000241400.1","gene_symbol":"AC022215.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141258418,"end":141258779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105229.6","gene_symbol":"PIAS4","gene_name":"protein inhibitor of activated STAT 4 [Source:HGNC Symbol;Acc:HGNC:17002]","synonyms":"ZMIZ6,PIASY,Piasg,FLJ12419","biotype":"protein_coding","ncbi_id":"51588","summary":null,"start":4007646,"end":4039386,"strand":1,"description":"protein inhibitor of activated STAT 4 [Source:HGNC Symbol;Acc:HGNC:17002]"}, {"versioned_ensembl_gene_id":"ENSG00000112964.13","gene_symbol":"GHR","gene_name":"growth hormone receptor [Source:HGNC Symbol;Acc:HGNC:4263]","synonyms":"GHBP","biotype":"protein_coding","ncbi_id":"2690","summary":"This gene encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011]","start":42423777,"end":42721878,"strand":1,"description":"growth hormone receptor [Source:HGNC Symbol;Acc:HGNC:4263]"}, {"versioned_ensembl_gene_id":"ENSG00000244161.1","gene_symbol":"FLNB-AS1","gene_name":"FLNB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40239]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105377105","summary":null,"start":58162547,"end":58170636,"strand":-1,"description":"FLNB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40239]"}, {"versioned_ensembl_gene_id":"ENSG00000263114.1","gene_symbol":"AC079953.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101234318,"end":101235053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230825.1","gene_symbol":"AC005532.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7255154,"end":7277779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237294.1","gene_symbol":"EIF4BP9","gene_name":"eukaryotic translation initiation factor 4B pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129692","summary":null,"start":66074835,"end":66076347,"strand":-1,"description":"eukaryotic translation initiation factor 4B pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37942]"}, {"versioned_ensembl_gene_id":"ENSG00000234288.1","gene_symbol":"OR1AA1P","gene_name":"olfactory receptor family 1 subfamily AA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14750]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"79312","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131424299,"end":131425214,"strand":1,"description":"olfactory receptor family 1 subfamily AA member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14750]"}, {"versioned_ensembl_gene_id":"ENSG00000281977.1","gene_symbol":"AC244131.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11192332,"end":11193253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226323.1","gene_symbol":"AC006150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14814131,"end":14816565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165935.9","gene_symbol":"SMCO2","gene_name":"single-pass membrane protein with coiled-coil domains 2 [Source:HGNC Symbol;Acc:HGNC:34448]","synonyms":"LOC341346,C12orf70","biotype":"protein_coding","ncbi_id":"341346","summary":null,"start":27466810,"end":27502185,"strand":1,"description":"single-pass membrane protein with coiled-coil domains 2 [Source:HGNC Symbol;Acc:HGNC:34448]"}, {"versioned_ensembl_gene_id":"ENSG00000100095.18","gene_symbol":"SEZ6L","gene_name":"seizure related 6 homolog like [Source:HGNC Symbol;Acc:HGNC:10763]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23544","summary":null,"start":26169474,"end":26383597,"strand":1,"description":"seizure related 6 homolog like [Source:HGNC Symbol;Acc:HGNC:10763]"}, {"versioned_ensembl_gene_id":"ENSG00000204640.1","gene_symbol":"NMS","gene_name":"neuromedin S [Source:HGNC Symbol;Acc:HGNC:32203]","synonyms":null,"biotype":"protein_coding","ncbi_id":"129521","summary":"This gene encodes a member of the neuromedin family of neuropeptides. The encoded preproprotein is proteolytically processed to generate a biologically active neuropeptide that plays a role in the regulation of circadian rhythm, anorexigenic action, antidiuretic action, cardiovascular function and stimulation of oxytocin and vasopressin release. [provided by RefSeq, May 2016]","start":100470482,"end":100483280,"strand":1,"description":"neuromedin S [Source:HGNC Symbol;Acc:HGNC:32203]"}, {"versioned_ensembl_gene_id":"ENSG00000224192.2","gene_symbol":"AL080273.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26241331,"end":26254092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242265.5","gene_symbol":"PEG10","gene_name":"paternally expressed 10 [Source:HGNC Symbol;Acc:HGNC:14005]","synonyms":"SIRH1,RTL2,RGAG3,MEF3L,Mart2,Mar2,KIAA1051,HB-1","biotype":"protein_coding","ncbi_id":"23089","summary":"This is a paternally expressed imprinted gene that is thought to have been derived from the Ty3/Gypsy family of retrotransposons. It contains two overlapping open reading frames, RF1 and RF2, and expresses two proteins: a shorter, gag-like protein (with a CCHC-type zinc finger domain) from RF1; and a longer, gag/pol-like fusion protein (with an additional aspartic protease motif) from RF1/RF2 by -1 translational frameshifting (-1 FS). While -1 FS has been observed in RNA viruses and transposons in both prokaryotes and eukaryotes, this gene represents the first example of -1 FS in a eukaryotic cellular gene. This gene is highly conserved across mammalian species and retains the heptanucleotide (GGGAAAC) and pseudoknot elements required for -1 FS. It is expressed in adult and embryonic tissues (most notably in placenta) and reported to have a role in cell proliferation, differentiation and apoptosis. Overexpression of this gene has been associated with several malignancies, such as hepatocellular carcinoma and B-cell lymphocytic leukemia. Knockout mice lacking this gene showed early embryonic lethality with placental defects, indicating the importance of this gene in embryonic development. Additional isoforms resulting from alternatively spliced transcript variants, and use of upstream non-AUG (CUG) start codon have been reported for this gene. [provided by RefSeq, Oct 2014]","start":94656325,"end":94669695,"strand":1,"description":"paternally expressed 10 [Source:HGNC Symbol;Acc:HGNC:14005]"}, {"versioned_ensembl_gene_id":"ENSG00000169504.14","gene_symbol":"CLIC4","gene_name":"chloride intracellular channel 4 [Source:HGNC Symbol;Acc:HGNC:13518]","synonyms":"P64H1,huH1,H1,DKFZP566G223,CLIC4L","biotype":"protein_coding","ncbi_id":"25932","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 4 (CLIC4) protein, encoded by the CLIC4 gene, is a member of the p64 family; the gene is expressed in many tissues and exhibits a intracellular vesicular pattern in Panc-1 cells (pancreatic cancer cells). [provided by RefSeq, Jul 2008]","start":24745357,"end":24844324,"strand":1,"description":"chloride intracellular channel 4 [Source:HGNC Symbol;Acc:HGNC:13518]"}, {"versioned_ensembl_gene_id":"ENSG00000232896.1","gene_symbol":"AL592463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110599475,"end":110605219,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229918.1","gene_symbol":"DOCK9-AS1","gene_name":"DOCK9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40672]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874096","summary":null,"start":98832084,"end":98834629,"strand":1,"description":"DOCK9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40672]"}, {"versioned_ensembl_gene_id":"ENSG00000278759.2","gene_symbol":"TBCD","gene_name":"tubulin folding cofactor D [Source:HGNC Symbol;Acc:HGNC:11581]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6904","summary":"Cofactor D is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. [provided by RefSeq, Jul 2008]","start":82923652,"end":82946138,"strand":1,"description":"tubulin folding cofactor D [Source:HGNC Symbol;Acc:HGNC:11581]"}, {"versioned_ensembl_gene_id":"ENSG00000226936.4","gene_symbol":"B3GALT4","gene_name":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]","synonyms":"GalT4,beta3Gal-T4","biotype":"protein_coding","ncbi_id":"8705","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is oriented telomere to centromere in close proximity to the ribosomal protein S18 gene. The functionality of the encoded protein is limited to ganglioseries glycolipid biosynthesis. [provided by RefSeq, Jul 2008]","start":33198732,"end":33200425,"strand":1,"description":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]"}, {"versioned_ensembl_gene_id":"ENSG00000230973.1","gene_symbol":"AL049734.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131437055,"end":131437670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225321.2","gene_symbol":"LINC01427","gene_name":"long intergenic non-protein coding RNA 1427 [Source:HGNC Symbol;Acc:HGNC:50737]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929663","summary":null,"start":22263065,"end":22284029,"strand":-1,"description":"long intergenic non-protein coding RNA 1427 [Source:HGNC Symbol;Acc:HGNC:50737]"}, {"versioned_ensembl_gene_id":"ENSG00000234671.1","gene_symbol":"MTCYBP5","gene_name":"mitochondrially encoded cytochrome b pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51967]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075125","summary":null,"start":57196638,"end":57197772,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51967]"}, {"versioned_ensembl_gene_id":"ENSG00000068831.18","gene_symbol":"RASGRP2","gene_name":"RAS guanyl releasing protein 2 [Source:HGNC Symbol;Acc:HGNC:9879]","synonyms":"CALDAG-GEFI","biotype":"protein_coding","ncbi_id":"10235","summary":"The protein encoded by this gene is a brain-enriched nucleotide exchanged factor that contains an N-terminal GEF domain, 2 tandem repeats of EF-hand calcium-binding motifs, and a C-terminal diacylglycerol/phorbol ester-binding domain. This protein can activate small GTPases, including RAS and RAP1/RAS3. The nucleotide exchange activity of this protein can be stimulated by calcium and diacylglycerol. Four alternatively spliced transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":64726911,"end":64745456,"strand":-1,"description":"RAS guanyl releasing protein 2 [Source:HGNC Symbol;Acc:HGNC:9879]"}, {"versioned_ensembl_gene_id":"ENSG00000279396.1","gene_symbol":"AC130469.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8575079,"end":8576170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237745.1","gene_symbol":"AC009963.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107914948,"end":107915286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268618.1","gene_symbol":"AC092316.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8549506,"end":8550139,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253649.3","gene_symbol":"PRSS51","gene_name":"protease, serine 51 [Source:HGNC Symbol;Acc:HGNC:37321]","synonyms":null,"biotype":"protein_coding","ncbi_id":"346702","summary":null,"start":10482878,"end":10547585,"strand":-1,"description":"protease, serine 51 [Source:HGNC Symbol;Acc:HGNC:37321]"}, {"versioned_ensembl_gene_id":"ENSG00000233494.1","gene_symbol":"AC009963.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107902997,"end":107903134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214024.2","gene_symbol":"RPL23AP29","gene_name":"ribosomal protein L23a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36355]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271458","summary":null,"start":153370612,"end":153371064,"strand":1,"description":"ribosomal protein L23a pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36355]"}, {"versioned_ensembl_gene_id":"ENSG00000143107.8","gene_symbol":"FNDC7","gene_name":"fibronectin type III domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26668]","synonyms":"FLJ35838","biotype":"protein_coding","ncbi_id":"163479","summary":null,"start":108712657,"end":108742740,"strand":1,"description":"fibronectin type III domain containing 7 [Source:HGNC Symbol;Acc:HGNC:26668]"}, {"versioned_ensembl_gene_id":"ENSG00000256084.1","gene_symbol":"AC092112.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14216590,"end":14221297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180139.11","gene_symbol":"ACTA2-AS1","gene_name":"ACTA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45169]","synonyms":"ZXF1,uc001kfo.1","biotype":"antisense_RNA","ncbi_id":"100132116","summary":null,"start":88932390,"end":88940820,"strand":1,"description":"ACTA2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45169]"}, {"versioned_ensembl_gene_id":"ENSG00000232470.1","gene_symbol":"AL136368.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":110869743,"end":110871594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253611.1","gene_symbol":"VN1R46P","gene_name":"vomeronasal 1 receptor 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:37366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131789","summary":null,"start":43219960,"end":43220809,"strand":-1,"description":"vomeronasal 1 receptor 46 pseudogene [Source:HGNC Symbol;Acc:HGNC:37366]"}, {"versioned_ensembl_gene_id":"ENSG00000226784.2","gene_symbol":"PGAM4","gene_name":"phosphoglycerate mutase family member 4 [Source:HGNC Symbol;Acc:HGNC:21731]","synonyms":"dJ1000K24.1,PGAM3,PGAM1,PGAM-B","biotype":"protein_coding","ncbi_id":"441531","summary":"This intronless gene appears to have arisen from a retrotransposition event, yet it is thought to be an expressed, protein-coding gene. The encoded protein is a member of the phosphoglycerate mutase family, a set of enzymes that catalyze the transfer of a phosphate group from 3-phosphoglycerate to 2-phosphoglycerate. [provided by RefSeq, May 2010]","start":77968874,"end":77969638,"strand":-1,"description":"phosphoglycerate mutase family member 4 [Source:HGNC Symbol;Acc:HGNC:21731]"}, {"versioned_ensembl_gene_id":"ENSG00000239797.1","gene_symbol":"RPL21P39","gene_name":"ribosomal protein L21 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36127]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389156","summary":null,"start":145824257,"end":145824739,"strand":-1,"description":"ribosomal protein L21 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:36127]"}, {"versioned_ensembl_gene_id":"ENSG00000244024.1","gene_symbol":"LARP7P4","gene_name":"La ribonucleoprotein domain family member 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49766]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421509","summary":null,"start":145523538,"end":145524415,"strand":1,"description":"La ribonucleoprotein domain family member 7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49766]"}, {"versioned_ensembl_gene_id":"ENSG00000206463.7","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:NCBI gene;Acc:394263]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":30973281,"end":30979676,"strand":1,"description":"mucin 21, cell surface associated [Source:NCBI gene;Acc:394263]"}, {"versioned_ensembl_gene_id":"ENSG00000164850.14","gene_symbol":"GPER1","gene_name":"G protein-coupled estrogen receptor 1 [Source:HGNC Symbol;Acc:HGNC:4485]","synonyms":"FEG-1,DRY12,CMKRL2,CEPR,LyGPR,LERGU2,LERGU,GPR30,GPER,GPCR-Br","biotype":"protein_coding","ncbi_id":"2852","summary":"This gene encodes a multi-pass membrane protein that localizes to the endoplasmic reticulum and a member of the G-protein coupled receptor 1 family. This receptor binds estrogen and activates multiple downstream signaling pathways, leading to stimulation of adenylate cyclase and an increase in cyclic AMP levels, while also promoting intracellular calcium mobilization and synthesis of phosphatidylinositol 3,4,5-trisphosphate in the nucleus. This protein therefore plays a role in the rapid nongenomic signaling events widely observed following stimulation of cells and tissues with estrogen. This receptor has been shown to play a role in diverse biological processes, including bone and nervous system development, metabolism, cognition, male fertility and uterine function. [provided by RefSeq, Aug 2017]","start":1082208,"end":1093815,"strand":1,"description":"G protein-coupled estrogen receptor 1 [Source:HGNC Symbol;Acc:HGNC:4485]"}, {"versioned_ensembl_gene_id":"ENSG00000137860.11","gene_symbol":"SLC28A2","gene_name":"solute carrier family 28 member 2 [Source:HGNC Symbol;Acc:HGNC:11002]","synonyms":"SPNT1,HsT17153,HCNT2,CNT2","biotype":"protein_coding","ncbi_id":"9153","summary":null,"start":45252230,"end":45277845,"strand":1,"description":"solute carrier family 28 member 2 [Source:HGNC Symbol;Acc:HGNC:11002]"}, {"versioned_ensembl_gene_id":"ENSG00000248180.1","gene_symbol":"GAPDHP60","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:4153]","synonyms":"GAPDL4,GAPDHL4","biotype":"processed_pseudogene","ncbi_id":"2601","summary":null,"start":87207092,"end":87208086,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:4153]"}, {"versioned_ensembl_gene_id":"ENSG00000204044.6","gene_symbol":"SLC12A5-AS1","gene_name":"SLC12A5 and MMP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53143]","synonyms":"RP11-465L10.10","biotype":"antisense_RNA","ncbi_id":"109729184","summary":null,"start":46013500,"end":46022073,"strand":-1,"description":"SLC12A5 and MMP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53143]"}, {"versioned_ensembl_gene_id":"ENSG00000146909.7","gene_symbol":"NOM1","gene_name":"nucleolar protein with MIF4G domain 1 [Source:HGNC Symbol;Acc:HGNC:13244]","synonyms":"SGD1,PPP1R113,C7orf3","biotype":"protein_coding","ncbi_id":"64434","summary":"Proteins that contain MIF4G (middle of eIF4G (MIM 600495)) and/or MA3 domains, such as NOM1, function in protein translation. These domains include binding sites for members of the EIF4A family of ATP-dependent DEAD box RNA helicases (see EIF4A1; MIM 602641) (Simmons et al., 2005 [PubMed 15715967]).[supplied by OMIM, Mar 2008]","start":156949723,"end":156973182,"strand":1,"description":"nucleolar protein with MIF4G domain 1 [Source:HGNC Symbol;Acc:HGNC:13244]"}, {"versioned_ensembl_gene_id":"ENSG00000198796.6","gene_symbol":"ALPK2","gene_name":"alpha kinase 2 [Source:HGNC Symbol;Acc:HGNC:20565]","synonyms":"HAK","biotype":"protein_coding","ncbi_id":"115701","summary":null,"start":58481247,"end":58628957,"strand":-1,"description":"alpha kinase 2 [Source:HGNC Symbol;Acc:HGNC:20565]"}, {"versioned_ensembl_gene_id":"ENSG00000267579.1","gene_symbol":"AC104971.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58557070,"end":58566677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231933.7","gene_symbol":"Z98949.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25876854,"end":25903247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235802.1","gene_symbol":"HCFC1-AS1","gene_name":"HCFC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40273]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873990","summary":null,"start":153969325,"end":153970087,"strand":1,"description":"HCFC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40273]"}, {"versioned_ensembl_gene_id":"ENSG00000230458.1","gene_symbol":"GPM6BP1","gene_name":"glycoprotein M6B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38782]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480720","summary":null,"start":18578417,"end":18578560,"strand":1,"description":"glycoprotein M6B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38782]"}, {"versioned_ensembl_gene_id":"ENSG00000158042.8","gene_symbol":"MRPL17","gene_name":"mitochondrial ribosomal protein L17 [Source:HGNC Symbol;Acc:HGNC:14053]","synonyms":"MRP-L26,RPML26","biotype":"protein_coding","ncbi_id":"63875","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. [provided by RefSeq, Jul 2008]","start":6680782,"end":6683401,"strand":-1,"description":"mitochondrial ribosomal protein L17 [Source:HGNC Symbol;Acc:HGNC:14053]"}, {"versioned_ensembl_gene_id":"ENSG00000178403.3","gene_symbol":"NEUROG2","gene_name":"neurogenin 2 [Source:HGNC Symbol;Acc:HGNC:13805]","synonyms":"ngn-2,Math4A,bHLHa8,Atoh4,NGN2","biotype":"protein_coding","ncbi_id":"63973","summary":"This gene encodes a neural-specific basic helix-loop-helix (bHLH) transcription factor that can specify a neuronal fate on ectodermal cells and is expressed in neural progenitor cells within the developing central and peripheral nervous systems. The protein product of this gene also plays a role in the differentiation and survival of midbrain dopaminergic neurons. [provided by RefSeq, Apr 2012]","start":112513516,"end":112516172,"strand":-1,"description":"neurogenin 2 [Source:HGNC Symbol;Acc:HGNC:13805]"}, {"versioned_ensembl_gene_id":"ENSG00000233184.6","gene_symbol":"AC093157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101025878,"end":101087268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115233.11","gene_symbol":"PSMD14","gene_name":"proteasome 26S subunit, non-ATPase 14 [Source:HGNC Symbol;Acc:HGNC:16889]","synonyms":"Rpn11,POH1,pad1","biotype":"protein_coding","ncbi_id":"10213","summary":"This gene encodes a component of the 26S proteasome. The 26S proteasome is a large multiprotein complex that catalyzes the degradation of ubiquitinated intracellular proteins. The encoded protein is a component of the 19S regulatory cap complex of the 26S proteasome and mediates substrate deubiquitination. A pseudogene of this gene is also located on the long arm of chromosome 2. [provided by RefSeq, Feb 2012]","start":161308038,"end":161411717,"strand":1,"description":"proteasome 26S subunit, non-ATPase 14 [Source:HGNC Symbol;Acc:HGNC:16889]"}, {"versioned_ensembl_gene_id":"ENSG00000231257.8","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"MEC17,C6orf134,FLJ13158,Em:AB023049.7","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30705297,"end":30725280,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000243958.7","gene_symbol":"PSMB9","gene_name":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]","synonyms":"LMP2,RING12,beta1i,PSMB6i","biotype":"protein_coding","ncbi_id":"5698","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 1 (proteasome beta 6 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. [provided by RefSeq, Mar 2010]","start":32934853,"end":32970271,"strand":1,"description":"proteasome subunit beta 9 [Source:HGNC Symbol;Acc:HGNC:9546]"}, {"versioned_ensembl_gene_id":"ENSG00000038382.18","gene_symbol":"TRIO","gene_name":"trio Rho guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:12303]","synonyms":"ARHGEF23","biotype":"protein_coding","ncbi_id":"7204","summary":"This gene encodes a large protein that functions as a GDP to GTP exchange factor. This protein promotes the reorganization of the actin cytoskeleton, thereby playing a role in cell migration and growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":14143702,"end":14532128,"strand":1,"description":"trio Rho guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:12303]"}, {"versioned_ensembl_gene_id":"ENSG00000235724.8","gene_symbol":"AC009299.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161222785,"end":161308303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163638.13","gene_symbol":"ADAMTS9","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 9 [Source:HGNC Symbol;Acc:HGNC:13202]","synonyms":"KIAA1312","biotype":"protein_coding","ncbi_id":"56999","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. Members of the ADAMTS family have been implicated in the cleavage of proteoglycans, the control of organ shape during development, and the inhibition of angiogenesis. This gene is localized to chromosome 3p14.3-p14.2, an area known to be lost in hereditary renal tumors. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Jan 2016]","start":64515654,"end":64688000,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 9 [Source:HGNC Symbol;Acc:HGNC:13202]"}, {"versioned_ensembl_gene_id":"ENSG00000230033.1","gene_symbol":"AC006357.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156944721,"end":156945645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232337.1","gene_symbol":"AC009313.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161048606,"end":161050546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135632.11","gene_symbol":"SMYD5","gene_name":"SMYD family member 5 [Source:HGNC Symbol;Acc:HGNC:16258]","synonyms":"ZMYND23,RRG1,RAI15,NN8-4AG","biotype":"protein_coding","ncbi_id":"10322","summary":null,"start":73214222,"end":73227237,"strand":1,"description":"SMYD family member 5 [Source:HGNC Symbol;Acc:HGNC:16258]"}, {"versioned_ensembl_gene_id":"ENSG00000274412.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"CD158B1,nkat6,CD158k,cl-43","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54763061,"end":54777585,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000167468.16","gene_symbol":"GPX4","gene_name":"glutathione peroxidase 4 [Source:HGNC Symbol;Acc:HGNC:4556]","synonyms":"PHGPx,MCSP","biotype":"protein_coding","ncbi_id":"2879","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme has a high preference for lipid hydroperoxides and protects cells against membrane lipid peroxidation and cell death. It is also required for normal sperm development; thus, it has been identified as a 'moonlighting' protein because of its ability to serve dual functions as a peroxidase, as well as a structural protein in mature spermatozoa. Mutations in this gene are associated with Sedaghatian type of spondylometaphyseal dysplasia (SMDS). This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Transcript variants resulting from alternative splicing or use of alternate promoters have been described to encode isoforms with different subcellular localization. [provided by RefSeq, Dec 2018]","start":1103926,"end":1106791,"strand":1,"description":"glutathione peroxidase 4 [Source:HGNC Symbol;Acc:HGNC:4556]"}, {"versioned_ensembl_gene_id":"ENSG00000282769.1","gene_symbol":"IGHD5-5","gene_name":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]","synonyms":"IGHD55,DK4","biotype":"IG_D_gene","ncbi_id":"28492","summary":null,"start":105913028,"end":105913047,"strand":-1,"description":"immunoglobulin heavy diversity 5-5 [Source:HGNC Symbol;Acc:HGNC:5511]"}, {"versioned_ensembl_gene_id":"ENSG00000105649.9","gene_symbol":"RAB3A","gene_name":"RAB3A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9777]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5864","summary":null,"start":18196784,"end":18204074,"strand":-1,"description":"RAB3A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9777]"}, {"versioned_ensembl_gene_id":"ENSG00000237004.3","gene_symbol":"ZNRF2P1","gene_name":"zinc and ring finger 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42792]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441208","summary":null,"start":32728569,"end":32729011,"strand":1,"description":"zinc and ring finger 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42792]"}, {"versioned_ensembl_gene_id":"ENSG00000238188.1","gene_symbol":"AL049733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130645723,"end":130646325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134313.15","gene_symbol":"KIDINS220","gene_name":"kinase D interacting substrate 220 [Source:HGNC Symbol;Acc:HGNC:29508]","synonyms":"ARMS","biotype":"protein_coding","ncbi_id":"57498","summary":"This gene encodes a transmembrane protein that is preferentially expressed in the nervous system where it controls neuronal cell survival, differentiation into exons and dendrites, and synaptic plasticity. The encoded protein interacts with membrane receptors, cytosolic signaling components, and cytoskeletal proteins, serving as a scaffold that mediates crosstalk between the neurotrophin pathway and several other intracellular signaling pathways. Aberrant expression of this gene is associated with the onset of various neuropsychiatric disorders and neurodegenerative diseases, including Alzheimer's disease. Naturally occurring mutations in this gene are associated with a syndrome characterized by spastic paraplegia, intellectual disability, nystagmus and obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":8721081,"end":8837630,"strand":-1,"description":"kinase D interacting substrate 220 [Source:HGNC Symbol;Acc:HGNC:29508]"}, {"versioned_ensembl_gene_id":"ENSG00000082701.14","gene_symbol":"GSK3B","gene_name":"glycogen synthase kinase 3 beta [Source:HGNC Symbol;Acc:HGNC:4617]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2932","summary":"The protein encoded by this gene is a serine-threonine kinase belonging to the glycogen synthase kinase subfamily. It is a negative regulator of glucose homeostasis and is involved in energy metabolism, inflammation, ER-stress, mitochondrial dysfunction, and apoptotic pathways. Defects in this gene have been associated with Parkinson disease and Alzheimer disease. [provided by RefSeq, Aug 2017]","start":119821323,"end":120094417,"strand":-1,"description":"glycogen synthase kinase 3 beta [Source:HGNC Symbol;Acc:HGNC:4617]"}, {"versioned_ensembl_gene_id":"ENSG00000272661.1","gene_symbol":"AC021097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151240399,"end":151240972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227494.2","gene_symbol":"USP9YP14","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38748]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107133502","summary":null,"start":18481087,"end":18487400,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:38748]"}, {"versioned_ensembl_gene_id":"ENSG00000196260.4","gene_symbol":"SFTA2","gene_name":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]","synonyms":"SFTPG","biotype":"protein_coding","ncbi_id":"389376","summary":null,"start":30931353,"end":30955636,"strand":-1,"description":"surfactant associated 2 [Source:HGNC Symbol;Acc:HGNC:18386]"}, {"versioned_ensembl_gene_id":"ENSG00000230034.8","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"D6S216E,PSMB5i,beta5i,LMP7,RING10","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32818694,"end":32822680,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000282038.1","gene_symbol":"AC243660.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28535031,"end":28535183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265681.7","gene_symbol":"RPL17","gene_name":"ribosomal protein L17 [Source:HGNC Symbol;Acc:HGNC:10307]","synonyms":"rpL23,L17","biotype":"protein_coding","ncbi_id":"6139","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L22P family of ribosomal proteins. It is located in the cytoplasm. This gene has been referred to as rpL23 because the encoded protein shares amino acid identity with ribosomal protein L23 from Halobacterium marismortui; however, its official symbol is RPL17. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring downstream C18orf32 (chromosome 18 open reading frame 32) gene. [provided by RefSeq, Dec 2010]","start":49488453,"end":49492523,"strand":-1,"description":"ribosomal protein L17 [Source:HGNC Symbol;Acc:HGNC:10307]"}, {"versioned_ensembl_gene_id":"ENSG00000204120.14","gene_symbol":"GIGYF2","gene_name":"GRB10 interacting GYF protein 2 [Source:HGNC Symbol;Acc:HGNC:11960]","synonyms":"TNRC15,PERQ3,PERQ2,PARK11,KIAA0642,GYF2","biotype":"protein_coding","ncbi_id":"26058","summary":"This gene contains CAG trinucleotide repeats and encodes a protein containing several stretches of polyglutamine residues. The encoded protein may be involved in the regulation of tyrosine kinase receptor signaling. This gene is located in a chromosomal region that was genetically linked to Parkinson disease type 11, and mutations in this gene were thought to be causative for this disease. However, more recent studies in different populations have been unable to replicate this association. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":232697299,"end":232860575,"strand":1,"description":"GRB10 interacting GYF protein 2 [Source:HGNC Symbol;Acc:HGNC:11960]"}, {"versioned_ensembl_gene_id":"ENSG00000249222.1","gene_symbol":"ATP5L2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G2 [Source:HGNC Symbol;Acc:HGNC:13213]","synonyms":"dJ222E13.5,ATP5K2","biotype":"protein_coding","ncbi_id":"267020","summary":null,"start":42639803,"end":42640601,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit G2 [Source:HGNC Symbol;Acc:HGNC:13213]"}, {"versioned_ensembl_gene_id":"ENSG00000281361.1","gene_symbol":"IGLVI-42","gene_name":"immunoglobulin lambda variable (I)-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5936]","synonyms":"IGLV(I)-42","biotype":"IG_V_pseudogene","ncbi_id":"28767","summary":null,"start":22397030,"end":22397522,"strand":1,"description":"immunoglobulin lambda variable (I)-42 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5936]"}, {"versioned_ensembl_gene_id":"ENSG00000146722.11","gene_symbol":"AC211486.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75391955,"end":75395434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230543.1","gene_symbol":"SNX3P1X","gene_name":"sorting nexin 3 pseudogene 1, X-linked [Source:HGNC Symbol;Acc:HGNC:41516]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873884","summary":null,"start":92515323,"end":92515497,"strand":-1,"description":"sorting nexin 3 pseudogene 1, X-linked [Source:HGNC Symbol;Acc:HGNC:41516]"}, {"versioned_ensembl_gene_id":"ENSG00000167658.15","gene_symbol":"EEF2","gene_name":"eukaryotic translation elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:3214]","synonyms":"EF2,EEF-2","biotype":"protein_coding","ncbi_id":"1938","summary":"This gene encodes a member of the GTP-binding translation elongation factor family. This protein is an essential factor for protein synthesis. It promotes the GTP-dependent translocation of the nascent protein chain from the A-site to the P-site of the ribosome. This protein is completely inactivated by EF-2 kinase phosporylation. [provided by RefSeq, Jul 2008]","start":3976056,"end":3985469,"strand":-1,"description":"eukaryotic translation elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:3214]"}, {"versioned_ensembl_gene_id":"ENSG00000227434.2","gene_symbol":"RNF19BPX","gene_name":"ring finger protein 19B pseudogene, X-linked [Source:HGNC Symbol;Acc:HGNC:38484]","synonyms":"RNF19BX","biotype":"processed_pseudogene","ncbi_id":"100419788","summary":null,"start":90209796,"end":90210420,"strand":-1,"description":"ring finger protein 19B pseudogene, X-linked [Source:HGNC Symbol;Acc:HGNC:38484]"}, {"versioned_ensembl_gene_id":"ENSG00000174326.11","gene_symbol":"SLC16A11","gene_name":"solute carrier family 16 member 11 [Source:HGNC Symbol;Acc:HGNC:23093]","synonyms":"MCT11,FLJ90193","biotype":"protein_coding","ncbi_id":"162515","summary":null,"start":7041630,"end":7043923,"strand":-1,"description":"solute carrier family 16 member 11 [Source:HGNC Symbol;Acc:HGNC:23093]"}, {"versioned_ensembl_gene_id":"ENSG00000058272.16","gene_symbol":"PPP1R12A","gene_name":"protein phosphatase 1 regulatory subunit 12A [Source:HGNC Symbol;Acc:HGNC:7618]","synonyms":"MBS,M130,MYPT1","biotype":"protein_coding","ncbi_id":"4659","summary":"Myosin phosphatase target subunit 1, which is also called the myosin-binding subunit of myosin phosphatase, is one of the subunits of myosin phosphatase. Myosin phosphatase regulates the interaction of actin and myosin downstream of the guanosine triphosphatase Rho. The small guanosine triphosphatase Rho is implicated in myosin light chain (MLC) phosphorylation, which results in contraction of smooth muscle and interaction of actin and myosin in nonmuscle cells. The guanosine triphosphate (GTP)-bound, active form of RhoA (GTP.RhoA) specifically interacted with the myosin-binding subunit (MBS) of myosin phosphatase, which regulates the extent of phosphorylation of MLC. Rho-associated kinase (Rho-kinase), which is activated by GTP. RhoA, phosphorylated MBS and consequently inactivated myosin phosphatase. Overexpression of RhoA or activated RhoA in NIH 3T3 cells increased phosphorylation of MBS and MLC. Thus, Rho appears to inhibit myosin phosphatase through the action of Rho-kinase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]","start":79773563,"end":79935460,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 12A [Source:HGNC Symbol;Acc:HGNC:7618]"}, {"versioned_ensembl_gene_id":"ENSG00000138308.5","gene_symbol":"PLA2G12B","gene_name":"phospholipase A2 group XIIB [Source:HGNC Symbol;Acc:HGNC:18555]","synonyms":"PLA2G13","biotype":"protein_coding","ncbi_id":"84647","summary":"The protein encoded by this gene belongs to the phospholipase A2 (PLA2) group of enzymes, which function in glycolipid hydrolysis with the release of free fatty acids and lysophospholipids. This family member has altered phospholipid-binding properties and is catalytically inactive. The protein is secreted, and together with microsomal triglyceride transfer protein, it functions to regulate HNF4alpha-induced hepatitis C virus infectivity. The expression of this gene is down-regulated in various tumors, suggesting that it may function as a negative regulator of tumor progression. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":72935170,"end":72954778,"strand":-1,"description":"phospholipase A2 group XIIB [Source:HGNC Symbol;Acc:HGNC:18555]"}, {"versioned_ensembl_gene_id":"ENSG00000274533.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54845266,"end":54856124,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000234256.2","gene_symbol":"PTCD2P2","gene_name":"pentatricopeptide repeat domain 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45168]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132487","summary":null,"start":88876450,"end":88877544,"strand":1,"description":"pentatricopeptide repeat domain 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45168]"}, {"versioned_ensembl_gene_id":"ENSG00000280794.1","gene_symbol":"AC226496.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68783028,"end":68783287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147894.14","gene_symbol":"C9orf72","gene_name":"chromosome 9 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:28337]","synonyms":"MGC23980,DENNL72","biotype":"protein_coding","ncbi_id":"203228","summary":"The protein encoded by this gene plays an important role in the regulation of endosomal trafficking, and has been shown to interact with Rab proteins that are involved in autophagy and endocytic transport. Expansion of a GGGGCC repeat from 2-22 copies to 700-1600 copies in the intronic sequence between alternate 5' exons in transcripts from this gene is associated with 9p-linked ALS (amyotrophic lateral sclerosis) and FTD (frontotemporal dementia) (PMID: 21944778, 21944779). Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA, and the accumulation of insoluble dipeptide repeat protein aggregates that could be pathogenic in FTD-ALS patients (PMID: 23393093). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2016]","start":27546545,"end":27573866,"strand":-1,"description":"chromosome 9 open reading frame 72 [Source:HGNC Symbol;Acc:HGNC:28337]"}, {"versioned_ensembl_gene_id":"ENSG00000248697.1","gene_symbol":"TOX4P1","gene_name":"TOX high mobility group box family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285412","summary":null,"start":112455924,"end":112457785,"strand":1,"description":"TOX high mobility group box family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44009]"}, {"versioned_ensembl_gene_id":"ENSG00000234186.2","gene_symbol":"C16orf82","gene_name":"chromosome 16 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:30755]","synonyms":"TNT","biotype":"protein_coding","ncbi_id":"162083","summary":null,"start":27066707,"end":27069165,"strand":1,"description":"chromosome 16 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:30755]"}, {"versioned_ensembl_gene_id":"ENSG00000108953.16","gene_symbol":"YWHAE","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]","synonyms":"FLJ45465","biotype":"protein_coding","ncbi_id":"7531","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 100% identical to the mouse ortholog. It interacts with CDC25 phosphatases, RAF1 and IRS1 proteins, suggesting its role in diverse biochemical activities related to signal transduction, such as cell division and regulation of insulin sensitivity. It has also been implicated in the pathogenesis of small cell lung cancer. Two transcript variants, one protein-coding and the other non-protein-coding, have been found for this gene. [provided by RefSeq, Aug 2008]","start":1344272,"end":1400378,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Source:HGNC Symbol;Acc:HGNC:12851]"}, {"versioned_ensembl_gene_id":"ENSG00000261482.1","gene_symbol":"AC092725.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27066928,"end":27067858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236481.1","gene_symbol":"LINC02195","gene_name":"long intergenic non-protein coding RNA 2195 [Source:HGNC Symbol;Acc:HGNC:53058]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371152","summary":null,"start":26584755,"end":26594813,"strand":-1,"description":"long intergenic non-protein coding RNA 2195 [Source:HGNC Symbol;Acc:HGNC:53058]"}, {"versioned_ensembl_gene_id":"ENSG00000254115.1","gene_symbol":"AC090572.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86707547,"end":86765023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168452.21","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32192849,"end":32211366,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000162607.12","gene_symbol":"USP1","gene_name":"ubiquitin specific peptidase 1 [Source:HGNC Symbol;Acc:HGNC:12607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7398","summary":"This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. The protein specifically deubiquitinates a protein in the Fanconi anemia (FA) DNA repair pathway. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]","start":62436297,"end":62451804,"strand":1,"description":"ubiquitin specific peptidase 1 [Source:HGNC Symbol;Acc:HGNC:12607]"}, {"versioned_ensembl_gene_id":"ENSG00000237194.1","gene_symbol":"SNAI1P1","gene_name":"snail family zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11129]","synonyms":"SNAI1P,SNAI1L1,SNAI1L","biotype":"processed_pseudogene","ncbi_id":"10415","summary":null,"start":209808804,"end":209809580,"strand":1,"description":"snail family zinc finger 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11129]"}, {"versioned_ensembl_gene_id":"ENSG00000228339.1","gene_symbol":"AMD1P1","gene_name":"adenosylmethionine decarboxylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44898]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133024","summary":null,"start":20350049,"end":20351100,"strand":1,"description":"adenosylmethionine decarboxylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44898]"}, {"versioned_ensembl_gene_id":"ENSG00000185909.14","gene_symbol":"KLHDC8B","gene_name":"kelch domain containing 8B [Source:HGNC Symbol;Acc:HGNC:28557]","synonyms":"MGC35097","biotype":"protein_coding","ncbi_id":"200942","summary":"This gene encodes a protein which forms a distinct beta-propeller protein structure of kelch domains allowing for protein-protein interactions. Mutations in this gene have been associated with Hodgkin lymphoma. [provided by RefSeq, Sep 2010]","start":49171611,"end":49176486,"strand":1,"description":"kelch domain containing 8B [Source:HGNC Symbol;Acc:HGNC:28557]"}, {"versioned_ensembl_gene_id":"ENSG00000235062.4","gene_symbol":"BCRP5","gene_name":"breakpoint cluster region pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1018]","synonyms":"BCRL5","biotype":"unprocessed_pseudogene","ncbi_id":"648980","summary":null,"start":20697962,"end":20698934,"strand":-1,"description":"breakpoint cluster region pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:1018]"}, {"versioned_ensembl_gene_id":"ENSG00000156469.8","gene_symbol":"MTERF3","gene_name":"mitochondrial transcription termination factor 3 [Source:HGNC Symbol;Acc:HGNC:24258]","synonyms":"MTERFD1,FLJ10939,CGI-12","biotype":"protein_coding","ncbi_id":"51001","summary":null,"start":96239398,"end":96261610,"strand":-1,"description":"mitochondrial transcription termination factor 3 [Source:HGNC Symbol;Acc:HGNC:24258]"}, {"versioned_ensembl_gene_id":"ENSG00000101391.20","gene_symbol":"CDK5RAP1","gene_name":"CDK5 regulatory subunit associated protein 1 [Source:HGNC Symbol;Acc:HGNC:15880]","synonyms":"C20orf34,HSPC167,CGI-05,C42","biotype":"protein_coding","ncbi_id":"51654","summary":"This gene encodes a regulator of cyclin-dependent kinase 5 activity. This protein has also been reported to modify RNA by adding a methylthio-group and may thus have a dual function as an RNA methylthiotransferase and as an inhibitor of cyclin-dependent kinase 5 activity. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, May 2013]","start":33358839,"end":33401561,"strand":-1,"description":"CDK5 regulatory subunit associated protein 1 [Source:HGNC Symbol;Acc:HGNC:15880]"}, {"versioned_ensembl_gene_id":"ENSG00000204389.9","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31815464,"end":31817946,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000280993.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195776180,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000166831.8","gene_symbol":"RBPMS2","gene_name":"RNA binding protein with multiple splicing 2 [Source:HGNC Symbol;Acc:HGNC:19098]","synonyms":null,"biotype":"protein_coding","ncbi_id":"348093","summary":"The protein encoded by this gene is a member of the RNA recognition motif (RRM)-containing protein family and is involved in the development and dedifferentiation of digestive smooth muscle cells. The encoded protein functions as a homodimer and indirectly inhibits the bone morphogenetic protein pathway. [provided by RefSeq, Aug 2016]","start":64739892,"end":64775587,"strand":-1,"description":"RNA binding protein with multiple splicing 2 [Source:HGNC Symbol;Acc:HGNC:19098]"}, {"versioned_ensembl_gene_id":"ENSG00000214821.4","gene_symbol":"HMGB1P4","gene_name":"high mobility group box 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4996]","synonyms":"HMGB1L4,HMG1L4P,HMG1L4","biotype":"processed_pseudogene","ncbi_id":"10355","summary":null,"start":170601662,"end":170602228,"strand":-1,"description":"high mobility group box 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4996]"}, {"versioned_ensembl_gene_id":"ENSG00000257786.1","gene_symbol":"AKIRIN1P1","gene_name":"akirin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50794]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418731","summary":null,"start":80561017,"end":80561560,"strand":-1,"description":"akirin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50794]"}, {"versioned_ensembl_gene_id":"ENSG00000257429.1","gene_symbol":"AC074031.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80583683,"end":80593701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000003393.14","gene_symbol":"ALS2","gene_name":"ALS2, alsin Rho guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:443]","synonyms":"ALS2CR6","biotype":"protein_coding","ncbi_id":"57679","summary":"The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":201700554,"end":201781189,"strand":-1,"description":"ALS2, alsin Rho guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:443]"}, {"versioned_ensembl_gene_id":"ENSG00000230799.1","gene_symbol":"AC007279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":201762737,"end":201763573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096872.15","gene_symbol":"IFT74","gene_name":"intraflagellar transport 74 [Source:HGNC Symbol;Acc:HGNC:21424]","synonyms":"CCDC2,FLJ22621,CMG1,CMG-1","biotype":"protein_coding","ncbi_id":"80173","summary":"This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome. [provided by RefSeq, Mar 2017]","start":26947039,"end":27062930,"strand":1,"description":"intraflagellar transport 74 [Source:HGNC Symbol;Acc:HGNC:21424]"}, {"versioned_ensembl_gene_id":"ENSG00000227912.1","gene_symbol":"AL441943.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2166332,"end":2169460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231305.3","gene_symbol":"AC112484.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128861313,"end":128871540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222046.2","gene_symbol":"DCDC2B","gene_name":"doublecortin domain containing 2B [Source:HGNC Symbol;Acc:HGNC:32576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149069","summary":"This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. [provided by RefSeq, Sep 2010]","start":32209094,"end":32216196,"strand":1,"description":"doublecortin domain containing 2B [Source:HGNC Symbol;Acc:HGNC:32576]"}, {"versioned_ensembl_gene_id":"ENSG00000273014.1","gene_symbol":"AC018645.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32758882,"end":32759353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100065.14","gene_symbol":"CARD10","gene_name":"caspase recruitment domain family member 10 [Source:HGNC Symbol;Acc:HGNC:16422]","synonyms":"CARMA3,BIMP1","biotype":"protein_coding","ncbi_id":"29775","summary":"The caspase recruitment domain (CARD) is a protein module that consists of 6 or 7 antiparallel alpha helices. It participates in apoptosis signaling through highly specific protein-protein homophilic interactions. Like several other CARD proteins, CARD10 belongs to the membrane-associated guanylate kinase (MAGUK) family and activates NF-kappa-B (NFKB; see MIM 164011) through BCL10 (MIM 603517) (Wang et al., 2001 [PubMed 11259443]).[supplied by OMIM, Mar 2008]","start":37490362,"end":37519542,"strand":-1,"description":"caspase recruitment domain family member 10 [Source:HGNC Symbol;Acc:HGNC:16422]"}, {"versioned_ensembl_gene_id":"ENSG00000237734.1","gene_symbol":"AL163192.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27391734,"end":27397563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235459.5","gene_symbol":"AC006463.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122681315,"end":122681662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072756.16","gene_symbol":"TRNT1","gene_name":"tRNA nucleotidyl transferase 1 [Source:HGNC Symbol;Acc:HGNC:17341]","synonyms":"MtCCA,CGI-47,CCA1","biotype":"protein_coding","ncbi_id":"51095","summary":"The protein encoded by this gene is a CCA-adding enzyme which belongs to the tRNA nucleotidyltransferase/poly(A) polymerase family. This essential enzyme functions by catalyzing the addition of the conserved nucleotide triplet CCA to the 3' terminus of tRNA molecules. Mutations in this gene result in sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":3126916,"end":3150879,"strand":1,"description":"tRNA nucleotidyl transferase 1 [Source:HGNC Symbol;Acc:HGNC:17341]"}, {"versioned_ensembl_gene_id":"ENSG00000145365.10","gene_symbol":"TIFA","gene_name":"TRAF interacting protein with forkhead associated domain [Source:HGNC Symbol;Acc:HGNC:19075]","synonyms":"TIFAA,T6BP,T2BP,MGC20791","biotype":"protein_coding","ncbi_id":"92610","summary":"This gene encodes an adapter protein involved in adaptive and innate immunity. This protein includes a forkhead-associated (FHA) domain that specifically binds to phosphorylated serine and threonine residues. In response to bacterial infection, the encoded host cell protein undergoes an intermolecular interaction between the FHA domain and a phosphorylated threonine that leads to protein oligomerization and stimulation of the NF-kappa B and other downstream signaling pathways. This protein exhibits reduced expression in hepatocellular carcinoma and may suppress hepatocellular carcinoma progression. This protein may also play a role in the DNA damage response. [provided by RefSeq, Jun 2018]","start":112274542,"end":112285903,"strand":-1,"description":"TRAF interacting protein with forkhead associated domain [Source:HGNC Symbol;Acc:HGNC:19075]"}, {"versioned_ensembl_gene_id":"ENSG00000278685.4","gene_symbol":"IQCA1L","gene_name":"IQ motif containing with AAA domain 1 like [Source:HGNC Symbol;Acc:HGNC:22831]","synonyms":"TCAG_9762,IQCA1P1","biotype":"protein_coding","ncbi_id":"392843","summary":null,"start":151190873,"end":151205496,"strand":-1,"description":"IQ motif containing with AAA domain 1 like [Source:HGNC Symbol;Acc:HGNC:22831]"}, {"versioned_ensembl_gene_id":"ENSG00000257735.1","gene_symbol":"AC090115.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48350945,"end":48442411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198797.6","gene_symbol":"BRINP2","gene_name":"BMP/retinoic acid inducible neural specific 2 [Source:HGNC Symbol;Acc:HGNC:13746]","synonyms":"DBCCR1L2,FAM5B","biotype":"protein_coding","ncbi_id":"57795","summary":null,"start":177171497,"end":177282422,"strand":1,"description":"BMP/retinoic acid inducible neural specific 2 [Source:HGNC Symbol;Acc:HGNC:13746]"}, {"versioned_ensembl_gene_id":"ENSG00000279509.1","gene_symbol":"AC007494.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47218026,"end":47218768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196421.8","gene_symbol":"C20orf204","gene_name":"chromosome 20 open reading frame 204 [Source:HGNC Symbol;Acc:HGNC:27655]","synonyms":"PRR17,NCRNA00176,LINC00176,FLJ27267,DKFZp434G015","biotype":"protein_coding","ncbi_id":"284739","summary":null,"start":64034344,"end":64039962,"strand":1,"description":"chromosome 20 open reading frame 204 [Source:HGNC Symbol;Acc:HGNC:27655]"}, {"versioned_ensembl_gene_id":"ENSG00000242726.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30318794,"end":30336373,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000214549.2","gene_symbol":"SDHCP2","gene_name":"succinate dehydrogenase complex subunit C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45177]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128302","summary":null,"start":92118664,"end":92119164,"strand":1,"description":"succinate dehydrogenase complex subunit C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45177]"}, {"versioned_ensembl_gene_id":"ENSG00000070031.3","gene_symbol":"SCT","gene_name":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6343","summary":"This gene encodes a member of the glucagon family of peptides. The encoded preproprotein is secreted by endocrine S cells in the proximal small intestinal mucosa as a prohormone, then proteolytically processed to generate the mature peptide hormone. The release of this active peptide hormone is stimulated by either fatty acids or acidic pH in the duodenum. This hormone stimulates the secretion of bile and bicarbonate in the duodenum, pancreatic and biliary ducts. [provided by RefSeq, Feb 2016]","start":626431,"end":627143,"strand":-1,"description":"secretin [Source:HGNC Symbol;Acc:HGNC:10607]"}, {"versioned_ensembl_gene_id":"ENSG00000280030.1","gene_symbol":"AC010329.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20746923,"end":20755250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254901.7","gene_symbol":"BORCS8","gene_name":"BLOC-1 related complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:37247]","synonyms":"MEF2BNB","biotype":"protein_coding","ncbi_id":"729991","summary":null,"start":19176903,"end":19192591,"strand":-1,"description":"BLOC-1 related complex subunit 8 [Source:HGNC Symbol;Acc:HGNC:37247]"}, {"versioned_ensembl_gene_id":"ENSG00000231311.1","gene_symbol":"PRYP2","gene_name":"PTPN13-like, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34019]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442864","summary":null,"start":18161366,"end":18176484,"strand":1,"description":"PTPN13-like, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34019]"}, {"versioned_ensembl_gene_id":"ENSG00000075391.16","gene_symbol":"RASAL2","gene_name":"RAS protein activator like 2 [Source:HGNC Symbol;Acc:HGNC:9874]","synonyms":"nGAP","biotype":"protein_coding","ncbi_id":"9462","summary":"This gene encodes a protein that contains the GAP-related domain (GRD), a characteristic domain of GTPase-activating proteins (GAPs). GAPs function as activators of Ras superfamily of small GTPases. The protein encoded by this gene is able to complement the defective RasGAP function in a yeast system. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":178094141,"end":178484147,"strand":1,"description":"RAS protein activator like 2 [Source:HGNC Symbol;Acc:HGNC:9874]"}, {"versioned_ensembl_gene_id":"ENSG00000273119.1","gene_symbol":"AP005229.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11390033,"end":11390729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169919.16","gene_symbol":"GUSB","gene_name":"glucuronidase beta [Source:HGNC Symbol;Acc:HGNC:4696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2990","summary":"This gene encodes a hydrolase that degrades glycosaminoglycans, including heparan sulfate, dermatan sulfate, and chondroitin-4,6-sulfate. The enzyme forms a homotetramer that is localized to the lysosome. Mutations in this gene result in mucopolysaccharidosis type VII. Alternative splicing results in multiple transcript variants. There are many pseudogenes of this locus in the human genome.[provided by RefSeq, May 2014]","start":65960684,"end":65982314,"strand":-1,"description":"glucuronidase beta [Source:HGNC Symbol;Acc:HGNC:4696]"}, {"versioned_ensembl_gene_id":"ENSG00000237954.7","gene_symbol":"AL445218.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95356229,"end":95381000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259553.5","gene_symbol":"AC140725.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101959848,"end":101961408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240471.1","gene_symbol":"PHBP8","gene_name":"prohibitin pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39287]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418804","summary":null,"start":119791829,"end":119792553,"strand":1,"description":"prohibitin pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39287]"}, {"versioned_ensembl_gene_id":"ENSG00000232744.1","gene_symbol":"USP9YP16","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38752]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478927","summary":null,"start":18121195,"end":18123799,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:38752]"}, {"versioned_ensembl_gene_id":"ENSG00000155621.14","gene_symbol":"C9orf85","gene_name":"chromosome 9 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:28784]","synonyms":"MGC61599","biotype":"protein_coding","ncbi_id":"138241","summary":null,"start":71911510,"end":71986054,"strand":1,"description":"chromosome 9 open reading frame 85 [Source:HGNC Symbol;Acc:HGNC:28784]"}, {"versioned_ensembl_gene_id":"ENSG00000255389.1","gene_symbol":"Z97989.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111599875,"end":111602295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111319.12","gene_symbol":"SCNN1A","gene_name":"sodium channel epithelial 1 alpha subunit [Source:HGNC Symbol;Acc:HGNC:10599]","synonyms":"SCNN1,ENaCalpha","biotype":"protein_coding","ncbi_id":"6337","summary":"Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the alpha subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), a rare salt wasting disease resulting from target organ unresponsiveness to mineralocorticoids. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2009]","start":6346843,"end":6377730,"strand":-1,"description":"sodium channel epithelial 1 alpha subunit [Source:HGNC Symbol;Acc:HGNC:10599]"}, {"versioned_ensembl_gene_id":"ENSG00000261369.1","gene_symbol":"AC007533.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47299447,"end":47317814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276473.1","gene_symbol":"AC107905.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61239906,"end":61240331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117298.14","gene_symbol":"ECE1","gene_name":"endothelin converting enzyme 1 [Source:HGNC Symbol;Acc:HGNC:3146]","synonyms":"ECE","biotype":"protein_coding","ncbi_id":"1889","summary":"The protein encoded by this gene is involved in proteolytic processing of endothelin precursors to biologically active peptides. Mutations in this gene are associated with Hirschsprung disease, cardiac defects and autonomic dysfunction. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Sep 2009]","start":21217247,"end":21345504,"strand":-1,"description":"endothelin converting enzyme 1 [Source:HGNC Symbol;Acc:HGNC:3146]"}, {"versioned_ensembl_gene_id":"ENSG00000257410.1","gene_symbol":"AC089984.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71793855,"end":71799627,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261628.1","gene_symbol":"AC087481.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30899480,"end":30900327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230214.1","gene_symbol":"FTLP18","gene_name":"ferritin light chain pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:37968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462786","summary":null,"start":36630335,"end":36630857,"strand":1,"description":"ferritin light chain pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:37968]"}, {"versioned_ensembl_gene_id":"ENSG00000136051.13","gene_symbol":"WASHC4","gene_name":"WASH complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:29174]","synonyms":"SWIP,KIAA1033","biotype":"protein_coding","ncbi_id":"23325","summary":"This gene encodes a component of the WASH complex, which functions in the intracellular transport of endosomes. Mutations in this gene have been detected in individuals with autosomal recessive cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":105107324,"end":105169134,"strand":1,"description":"WASH complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:29174]"}, {"versioned_ensembl_gene_id":"ENSG00000257109.3","gene_symbol":"OR4F28P","gene_name":"olfactory receptor family 4 subfamily F member 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:31229]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390652","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101875964,"end":101876901,"strand":1,"description":"olfactory receptor family 4 subfamily F member 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:31229]"}, {"versioned_ensembl_gene_id":"ENSG00000259688.1","gene_symbol":"AC019288.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35396221,"end":35396444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273716.2","gene_symbol":"AC092670.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118460224,"end":118460301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261629.1","gene_symbol":"AC005692.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141429711,"end":141431268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168556.6","gene_symbol":"ING2","gene_name":"inhibitor of growth family member 2 [Source:HGNC Symbol;Acc:HGNC:6063]","synonyms":"p33ING2,ING1L","biotype":"protein_coding","ncbi_id":"3622","summary":"This gene is a member of the inhibitor of growth (ING) family. Members of the ING family associate with and modulate the activity of histone acetyltransferase (HAT) and histone deacetylase (HDAC) complexes and function in DNA repair and apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":183504994,"end":183511096,"strand":1,"description":"inhibitor of growth family member 2 [Source:HGNC Symbol;Acc:HGNC:6063]"}, {"versioned_ensembl_gene_id":"ENSG00000225639.1","gene_symbol":"PGAM1P2","gene_name":"phosphoglycerate mutase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42449]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392310","summary":null,"start":35943210,"end":35943934,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42449]"}, {"versioned_ensembl_gene_id":"ENSG00000267551.3","gene_symbol":"AC005264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3141576,"end":3155175,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258968.2","gene_symbol":"AL049830.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31018446,"end":31018796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243107.1","gene_symbol":"AC000120.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":92200014,"end":92206857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274775.2","gene_symbol":"Z82195.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130445085,"end":130524257,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273822.5","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195744429,"end":195789161,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000274823.1","gene_symbol":"AC025574.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56376818,"end":56377331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230316.6","gene_symbol":"FEZF1-AS1","gene_name":"FEZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41001]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"154860","summary":null,"start":122303658,"end":122310077,"strand":1,"description":"FEZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41001]"}, {"versioned_ensembl_gene_id":"ENSG00000263753.6","gene_symbol":"LINC00667","gene_name":"long intergenic non-protein coding RNA 667 [Source:HGNC Symbol;Acc:HGNC:27906]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339290","summary":null,"start":5237826,"end":5246508,"strand":1,"description":"long intergenic non-protein coding RNA 667 [Source:HGNC Symbol;Acc:HGNC:27906]"}, {"versioned_ensembl_gene_id":"ENSG00000180357.9","gene_symbol":"ZNF609","gene_name":"zinc finger protein 609 [Source:HGNC Symbol;Acc:HGNC:29003]","synonyms":"KIAA0295","biotype":"protein_coding","ncbi_id":"23060","summary":null,"start":64460742,"end":64686068,"strand":1,"description":"zinc finger protein 609 [Source:HGNC Symbol;Acc:HGNC:29003]"}, {"versioned_ensembl_gene_id":"ENSG00000266153.1","gene_symbol":"AP005380.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5159332,"end":5171026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279160.1","gene_symbol":"AC009336.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":176189919,"end":176192538,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231824.3","gene_symbol":"AKAIN1","gene_name":"A-kinase anchor inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28285]","synonyms":"C18orf42","biotype":"protein_coding","ncbi_id":"642597","summary":null,"start":5145285,"end":5197503,"strand":-1,"description":"A-kinase anchor inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:28285]"}, {"versioned_ensembl_gene_id":"ENSG00000280909.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHALP2,SDHAL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000257515.1","gene_symbol":"AC011601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71709171,"end":71710374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272295.1","gene_symbol":"AL844853.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31962758,"end":31973199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260290.2","gene_symbol":"AC092115.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69756536,"end":69757937,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231189.1","gene_symbol":"AC013448.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":223498773,"end":223504611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182854.8","gene_symbol":"OR4F15","gene_name":"olfactory receptor family 4 subfamily F member 15 [Source:HGNC Symbol;Acc:HGNC:15078]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390649","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":101812202,"end":101820197,"strand":1,"description":"olfactory receptor family 4 subfamily F member 15 [Source:HGNC Symbol;Acc:HGNC:15078]"}, {"versioned_ensembl_gene_id":"ENSG00000270131.1","gene_symbol":"AP003465.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96140572,"end":96140944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259660.2","gene_symbol":"DNM1P47","gene_name":"dynamin 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:35200]","synonyms":"DNM1DN14@,DNM1DN14-3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100216544","summary":null,"start":101751032,"end":101794302,"strand":1,"description":"dynamin 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:35200]"}, {"versioned_ensembl_gene_id":"ENSG00000100024.14","gene_symbol":"UPB1","gene_name":"beta-ureidopropionase 1 [Source:HGNC Symbol;Acc:HGNC:16297]","synonyms":"BUP1","biotype":"protein_coding","ncbi_id":"51733","summary":"This gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity. [provided by RefSeq, Jul 2008]","start":24494107,"end":24528390,"strand":1,"description":"beta-ureidopropionase 1 [Source:HGNC Symbol;Acc:HGNC:16297]"}, {"versioned_ensembl_gene_id":"ENSG00000235014.1","gene_symbol":"REREP2Y","gene_name":"arginine-glutamic acid dipeptide repeats pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:38796]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"105377243","summary":null,"start":26198331,"end":26208148,"strand":-1,"description":"arginine-glutamic acid dipeptide repeats pseudogene 2, Y-linked [Source:HGNC Symbol;Acc:HGNC:38796]"}, {"versioned_ensembl_gene_id":"ENSG00000283503.1","gene_symbol":"LINC01902","gene_name":"long intergenic non-protein coding RNA 1902 [Source:HGNC Symbol;Acc:HGNC:52721]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372079","summary":null,"start":39841809,"end":39896298,"strand":1,"description":"long intergenic non-protein coding RNA 1902 [Source:HGNC Symbol;Acc:HGNC:52721]"}, {"versioned_ensembl_gene_id":"ENSG00000122481.16","gene_symbol":"RWDD3","gene_name":"RWD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21393]","synonyms":"DKFZP566K023","biotype":"protein_coding","ncbi_id":"25950","summary":null,"start":95234155,"end":95247225,"strand":1,"description":"RWD domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21393]"}, {"versioned_ensembl_gene_id":"ENSG00000231992.1","gene_symbol":"AC092802.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":95120147,"end":95138554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226026.5","gene_symbol":"AC092802.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95163219,"end":95233982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231702.2","gene_symbol":"AL645608.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1008076,"end":1008229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124787.13","gene_symbol":"RPP40","gene_name":"ribonuclease P/MRP subunit p40 [Source:HGNC Symbol;Acc:HGNC:20992]","synonyms":"RNASEP1,bA428J1.3","biotype":"protein_coding","ncbi_id":"10799","summary":null,"start":4994732,"end":5004063,"strand":-1,"description":"ribonuclease P/MRP subunit p40 [Source:HGNC Symbol;Acc:HGNC:20992]"}, {"versioned_ensembl_gene_id":"ENSG00000205682.2","gene_symbol":"AC020741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61420246,"end":61428221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275421.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54847678,"end":54861692,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000110076.18","gene_symbol":"NRXN2","gene_name":"neurexin 2 [Source:HGNC Symbol;Acc:HGNC:8009]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9379","summary":"This gene encodes a member of the neurexin gene family. The products of these genes function as cell adhesion molecules and receptors in the vertebrate nervous system. These genes utilize two promoters. The majority of transcripts are produced from the upstream promoter and encode alpha-neurexin isoforms while a smaller number of transcripts are produced from the downstream promoter and encode beta-neuresin isoforms. The alpha-neurexins contain epidermal growth factor-like (EGF-like) sequences and laminin G domains, and have been shown to interact with neurexophilins. The beta-neurexins lack EGF-like sequences and contain fewer laminin G domains than alpha-neurexins. Alternative splicing and the use of alternative promoters may generate thousands of transcript variants (PMID: 12036300, PMID: 11944992).[provided by RefSeq, Jun 2010]","start":64606174,"end":64723188,"strand":-1,"description":"neurexin 2 [Source:HGNC Symbol;Acc:HGNC:8009]"}, {"versioned_ensembl_gene_id":"ENSG00000280396.1","gene_symbol":"AC114546.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34999902,"end":35000270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269957.5","gene_symbol":"AL353811.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24545952,"end":24591993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206409.8","gene_symbol":"APOM","gene_name":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]","synonyms":"G3a,ApoM,NG20","biotype":"protein_coding","ncbi_id":"55937","summary":"The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]","start":31642642,"end":31648435,"strand":1,"description":"apolipoprotein M [Source:HGNC Symbol;Acc:HGNC:13916]"}, {"versioned_ensembl_gene_id":"ENSG00000260979.1","gene_symbol":"AC022167.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8962706,"end":8966990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248462.1","gene_symbol":"NENFP3","gene_name":"neudesin neurotrophic factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50300]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481703","summary":null,"start":13553654,"end":13553966,"strand":-1,"description":"neudesin neurotrophic factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50300]"}, {"versioned_ensembl_gene_id":"ENSG00000224766.1","gene_symbol":"BX005460.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31876448,"end":31876741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277354.1","gene_symbol":"CRIM1","gene_name":"cysteine rich transmembrane BMP regulator 1 [Source:HGNC Symbol;Acc:HGNC:2359]","synonyms":"S52","biotype":"protein_coding","ncbi_id":"51232","summary":"This gene encodes a transmembrane protein containing six cysteine-rich repeat domains and an insulin-like growth factor-binding domain. The encoded protein may play a role in tissue development though interactions with members of the transforming growth factor beta family, such as bone morphogenetic proteins. [provided by RefSeq, Nov 2010]","start":36361959,"end":36362656,"strand":1,"description":"cysteine rich transmembrane BMP regulator 1 [Source:HGNC Symbol;Acc:HGNC:2359]"}, {"versioned_ensembl_gene_id":"ENSG00000211802.3","gene_symbol":"TRAV22","gene_name":"T-cell receptor alpha variable 22 [Source:HGNC Symbol;Acc:HGNC:12119]","synonyms":"TCRAV22S1,TCRAV13S1","biotype":"TR_V_gene","ncbi_id":"28661","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22070557,"end":22071208,"strand":1,"description":"T-cell receptor alpha variable 22 [Source:HGNC Symbol;Acc:HGNC:12119]"}, {"versioned_ensembl_gene_id":"ENSG00000147262.3","gene_symbol":"GPR119","gene_name":"G protein-coupled receptor 119 [Source:HGNC Symbol;Acc:HGNC:19060]","synonyms":"hGPCR2,GPCR2","biotype":"protein_coding","ncbi_id":"139760","summary":"This gene encodes a member of the rhodopsin subfamily of G-protein-coupled receptors that is expressed in the pancreas and gastrointestinal tract. The encoded protein is activated by lipid amides including lysophosphatidylcholine and oleoylethanolamide and may be involved in glucose homeostasis. This protein is a potential drug target in the treatment of type 2 diabetes.[provided by RefSeq, Jan 2010]","start":130384440,"end":130385447,"strand":-1,"description":"G protein-coupled receptor 119 [Source:HGNC Symbol;Acc:HGNC:19060]"}, {"versioned_ensembl_gene_id":"ENSG00000224989.2","gene_symbol":"FAM41AY1","gene_name":"family with sequence similarity 41 member A, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:23955]","synonyms":"FAM41AY","biotype":"lincRNA","ncbi_id":"340618","summary":null,"start":17500958,"end":17515018,"strand":1,"description":"family with sequence similarity 41 member A, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:23955]"}, {"versioned_ensembl_gene_id":"ENSG00000268836.1","gene_symbol":"Z69706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":185748,"end":186294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235617.1","gene_symbol":"AC016027.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18101612,"end":18101888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271167.1","gene_symbol":"LINC01109","gene_name":"long intergenic non-protein coding RNA 1109 [Source:HGNC Symbol;Acc:HGNC:49235]","synonyms":"lncRNA-N1","biotype":"lincRNA","ncbi_id":"102216341","summary":null,"start":76404058,"end":76407138,"strand":1,"description":"long intergenic non-protein coding RNA 1109 [Source:HGNC Symbol;Acc:HGNC:49235]"}, {"versioned_ensembl_gene_id":"ENSG00000226485.1","gene_symbol":"RBM22P3","gene_name":"RNA binding motif protein 22 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39696]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128867","summary":null,"start":56490682,"end":56491635,"strand":1,"description":"RNA binding motif protein 22 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39696]"}, {"versioned_ensembl_gene_id":"ENSG00000206172.8","gene_symbol":"HBA1","gene_name":"hemoglobin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:4823]","synonyms":"HBA-T3","biotype":"protein_coding","ncbi_id":"3039","summary":"The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq, Jul 2008]","start":176680,"end":177522,"strand":1,"description":"hemoglobin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:4823]"}, {"versioned_ensembl_gene_id":"ENSG00000185250.15","gene_symbol":"PPIL6","gene_name":"peptidylprolyl isomerase like 6 [Source:HGNC Symbol;Acc:HGNC:21557]","synonyms":"RSPH12,MGC41939,dJ919F19.1,bA425D10.6","biotype":"protein_coding","ncbi_id":"285755","summary":null,"start":109390215,"end":109441171,"strand":-1,"description":"peptidylprolyl isomerase like 6 [Source:HGNC Symbol;Acc:HGNC:21557]"}, {"versioned_ensembl_gene_id":"ENSG00000224374.1","gene_symbol":"AL023693.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135259996,"end":135260933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255229.1","gene_symbol":"AC069287.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129279,"end":186136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251106.1","gene_symbol":"FAM206BP","gene_name":"family with sequence similarity 206 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39851]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390403","summary":null,"start":46270077,"end":46270617,"strand":1,"description":"family with sequence similarity 206 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:39851]"}, {"versioned_ensembl_gene_id":"ENSG00000232897.2","gene_symbol":"AL117329.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47662559,"end":47663603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243915.1","gene_symbol":"THAP12P2","gene_name":"THAP domain containing 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39566]","synonyms":"PRKRIRP2","biotype":"processed_pseudogene","ncbi_id":"100422711","summary":null,"start":86012561,"end":86015120,"strand":1,"description":"THAP domain containing 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39566]"}, {"versioned_ensembl_gene_id":"ENSG00000249815.1","gene_symbol":"AC004704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111826881,"end":112072698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255641.1","gene_symbol":"AC068775.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10412312,"end":10436001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250556.1","gene_symbol":"CCDC34P1","gene_name":"coiled-coil domain containing 34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288584","summary":null,"start":112068010,"end":112068526,"strand":1,"description":"coiled-coil domain containing 34 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44008]"}, {"versioned_ensembl_gene_id":"ENSG00000275600.2","gene_symbol":"PIGW","gene_name":"phosphatidylinositol glycan anchor biosynthesis class W [Source:HGNC Symbol;Acc:HGNC:23213]","synonyms":"FLJ37433,Gwt1","biotype":"protein_coding","ncbi_id":"284098","summary":"The protein encoded by this gene is an inositol acyltransferase that acylates the inositol ring of phosphatidylinositol. This occurs in the endoplasmic reticulum and is a step in the biosynthesis of glycosylphosphatidylinositol (GPI), which anchors many cell surface proteins to the membrane. Defects in this gene are a cause of the age-dependent epileptic encephalopathy West syndrome as well as a syndrome exhibiting hyperphosphatasia and cognitive disability (HPMRS5). [provided by RefSeq, Jul 2017]","start":36535392,"end":36539682,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class W [Source:HGNC Symbol;Acc:HGNC:23213]"}, {"versioned_ensembl_gene_id":"ENSG00000234469.4","gene_symbol":"CLDN34","gene_name":"claudin 34 [Source:HGNC Symbol;Acc:HGNC:51259]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288814","summary":null,"start":9967358,"end":9968352,"strand":1,"description":"claudin 34 [Source:HGNC Symbol;Acc:HGNC:51259]"}, {"versioned_ensembl_gene_id":"ENSG00000231135.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"KIAA0170,Em:AB023051.5,NFBD1","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30692058,"end":30710140,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000172432.18","gene_symbol":"GTPBP2","gene_name":"GTP binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4670]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54676","summary":"GTP-binding proteins, or G proteins, constitute a superfamily capable of binding GTP or GDP. G proteins are activated by binding GTP and are inactivated by hydrolyzing GTP to GDP. This general mechanism enables G proteins to perform a wide range of biologic activities.[supplied by OMIM, Jan 2003]","start":43605316,"end":43629162,"strand":-1,"description":"GTP binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4670]"}, {"versioned_ensembl_gene_id":"ENSG00000251491.2","gene_symbol":"OR7E28P","gene_name":"olfactory receptor family 7 subfamily E member 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:8400]","synonyms":"OST128,OR7E27P,OR7E133P,OR7E107P,hg616","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"26645","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158862311,"end":158863285,"strand":1,"description":"olfactory receptor family 7 subfamily E member 28 pseudogene [Source:HGNC Symbol;Acc:HGNC:8400]"}, {"versioned_ensembl_gene_id":"ENSG00000106560.10","gene_symbol":"GIMAP2","gene_name":"GTPase, IMAP family member 2 [Source:HGNC Symbol;Acc:HGNC:21789]","synonyms":"IMAP2,IAN12,HIMAP2,DKFZp586D0824","biotype":"protein_coding","ncbi_id":"26157","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]","start":150685697,"end":150693641,"strand":1,"description":"GTPase, IMAP family member 2 [Source:HGNC Symbol;Acc:HGNC:21789]"}, {"versioned_ensembl_gene_id":"ENSG00000263159.1","gene_symbol":"AC005736.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4032012,"end":4032936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227788.1","gene_symbol":"MTCO3P43","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52146]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075190","summary":null,"start":120211727,"end":120212862,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:52146]"}, {"versioned_ensembl_gene_id":"ENSG00000213877.3","gene_symbol":"CFL1P7","gene_name":"cofilin 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39959]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505919","summary":null,"start":25324174,"end":25324659,"strand":1,"description":"cofilin 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39959]"}, {"versioned_ensembl_gene_id":"ENSG00000241648.1","gene_symbol":"CADM2-AS2","gene_name":"CADM2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41247]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874037","summary":null,"start":85799987,"end":85828050,"strand":-1,"description":"CADM2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:41247]"}, {"versioned_ensembl_gene_id":"ENSG00000149488.12","gene_symbol":"TMC2","gene_name":"transmembrane channel like 2 [Source:HGNC Symbol;Acc:HGNC:16527]","synonyms":"dJ686C3.3,C20orf145","biotype":"protein_coding","ncbi_id":"117532","summary":"This gene encodes a transmembrane protein that is necesssary for mechanotransduction in cochlear hair cells of the inner ear. Mutations in this gene may underlie hereditary disorders of balance and hearing. [provided by RefSeq, Aug 2015]","start":2536607,"end":2641784,"strand":1,"description":"transmembrane channel like 2 [Source:HGNC Symbol;Acc:HGNC:16527]"}, {"versioned_ensembl_gene_id":"ENSG00000133858.15","gene_symbol":"ZFC3H1","gene_name":"zinc finger C3H1-type containing [Source:HGNC Symbol;Acc:HGNC:28328]","synonyms":"PSRC2,MGC23401,KIAA0546,CSRC2,CCDC131","biotype":"protein_coding","ncbi_id":"196441","summary":null,"start":71609472,"end":71667725,"strand":-1,"description":"zinc finger C3H1-type containing [Source:HGNC Symbol;Acc:HGNC:28328]"}, {"versioned_ensembl_gene_id":"ENSG00000270680.1","gene_symbol":"AL596092.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29339566,"end":29339869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270377.1","gene_symbol":"AC097639.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32243847,"end":32244018,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275730.4","gene_symbol":"LILRB4","gene_name":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]","synonyms":"LIR-5,ILT3,HM18,LIR5,CD85k","biotype":"protein_coding","ncbi_id":"11006","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54671018,"end":54678557,"strand":1,"description":"leukocyte immunoglobulin like receptor B4 [Source:HGNC Symbol;Acc:HGNC:6608]"}, {"versioned_ensembl_gene_id":"ENSG00000232953.1","gene_symbol":"HSPA8P18","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:44933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402125","summary":null,"start":19940269,"end":19943310,"strand":-1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:44933]"}, {"versioned_ensembl_gene_id":"ENSG00000236131.1","gene_symbol":"MED13P1","gene_name":"mediator complex subunit 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38733]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100499481","summary":null,"start":14907898,"end":14908068,"strand":1,"description":"mediator complex subunit 13 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38733]"}, {"versioned_ensembl_gene_id":"ENSG00000177400.6","gene_symbol":"OR7E8P","gene_name":"olfactory receptor family 7 subfamily E member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8458]","synonyms":"OR11-11a","biotype":"unprocessed_pseudogene","ncbi_id":"346708","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":12684154,"end":12685153,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 8 pseudogene [Source:HGNC Symbol;Acc:HGNC:8458]"}, {"versioned_ensembl_gene_id":"ENSG00000177853.14","gene_symbol":"ZNF518A","gene_name":"zinc finger protein 518A [Source:HGNC Symbol;Acc:HGNC:29009]","synonyms":"ZNF518,KIAA0335","biotype":"protein_coding","ncbi_id":"9849","summary":"The protein encoded by this gene is a member of the krueppel C2H2-type zinc finger protein family. The encoded protein contains five zinc fingers and is likely a nuclear transcriptional regulator. Numerous transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2016]","start":96129715,"end":96205288,"strand":1,"description":"zinc finger protein 518A [Source:HGNC Symbol;Acc:HGNC:29009]"}, {"versioned_ensembl_gene_id":"ENSG00000197092.5","gene_symbol":"GOLGA6L16P","gene_name":"golgin A6 family-like 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:38117]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287845","summary":null,"start":25495651,"end":25501958,"strand":-1,"description":"golgin A6 family-like 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:38117]"}, {"versioned_ensembl_gene_id":"ENSG00000261905.1","gene_symbol":"AC217785.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155225758,"end":155229107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133574.9","gene_symbol":"GIMAP4","gene_name":"GTPase, IMAP family member 4 [Source:HGNC Symbol;Acc:HGNC:21872]","synonyms":"IMAP4,IAN1,HIMAP4,FLJ11110","biotype":"protein_coding","ncbi_id":"55303","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. The encoded protein of this gene may be negatively regulated by T-cell acute lymphocytic leukemia 1 (TAL1). In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]","start":150567277,"end":150573955,"strand":1,"description":"GTPase, IMAP family member 4 [Source:HGNC Symbol;Acc:HGNC:21872]"}, {"versioned_ensembl_gene_id":"ENSG00000223876.1","gene_symbol":"RPS27P1","gene_name":"ribosomal protein S27 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23740]","synonyms":"bA108M11.3","biotype":"processed_pseudogene","ncbi_id":"414228","summary":null,"start":91544852,"end":91545098,"strand":1,"description":"ribosomal protein S27 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23740]"}, {"versioned_ensembl_gene_id":"ENSG00000237413.5","gene_symbol":"MGC27382","gene_name":"uncharacterized MGC27382 [Source:NCBI gene;Acc:149047]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"149047","summary":null,"start":78229599,"end":78369464,"strand":1,"description":"uncharacterized MGC27382 [Source:NCBI gene;Acc:149047]"}, {"versioned_ensembl_gene_id":"ENSG00000141429.13","gene_symbol":"GALNT1","gene_name":"polypeptide N-acetylgalactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4123]","synonyms":"GalNAc-T1","biotype":"protein_coding","ncbi_id":"2589","summary":"This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. Transcript variants derived from this gene that utilize alternative polyA signals have been described in the literature. [provided by RefSeq, Jul 2008]","start":35581117,"end":35711834,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4123]"}, {"versioned_ensembl_gene_id":"ENSG00000273686.4","gene_symbol":"B2M","gene_name":"beta-2-microglobulin [Source:HGNC Symbol;Acc:HGNC:914]","synonyms":null,"biotype":"protein_coding","ncbi_id":"567","summary":"This gene encodes a serum protein found in association with the major histocompatibility complex (MHC) class I heavy chain on the surface of nearly all nucleated cells. The protein has a predominantly beta-pleated sheet structure that can form amyloid fibrils in some pathological conditions. The encoded antimicrobial protein displays antibacterial activity in amniotic fluid. A mutation in this gene has been shown to result in hypercatabolic hypoproteinemia.[provided by RefSeq, Aug 2014]","start":44711489,"end":44718888,"strand":1,"description":"beta-2-microglobulin [Source:HGNC Symbol;Acc:HGNC:914]"}, {"versioned_ensembl_gene_id":"ENSG00000136167.13","gene_symbol":"LCP1","gene_name":"lymphocyte cytosolic protein 1 [Source:HGNC Symbol;Acc:HGNC:6528]","synonyms":"PLS2,LC64P,L-PLASTIN,CP64","biotype":"protein_coding","ncbi_id":"3936","summary":"Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. Plastin 1 (otherwise known as Fimbrin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has been found in all other normal cells of solid tissues that have replicative potential (fibroblasts, endothelial cells, epithelial cells, melanocytes, etc.). However, L-plastin has been found in many types of malignant human cells of non-hemopoietic origin suggesting that its expression is induced accompanying tumorigenesis in solid tissues. [provided by RefSeq, Jul 2008]","start":46125920,"end":46211871,"strand":-1,"description":"lymphocyte cytosolic protein 1 [Source:HGNC Symbol;Acc:HGNC:6528]"}, {"versioned_ensembl_gene_id":"ENSG00000254620.1","gene_symbol":"AL050327.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58594417,"end":58603973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171115.3","gene_symbol":"GIMAP8","gene_name":"GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:HGNC:21792]","synonyms":"IAN9,hIAN6,DKFZp667I133","biotype":"protein_coding","ncbi_id":"155038","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]","start":150450630,"end":150479392,"strand":1,"description":"GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:HGNC:21792]"}, {"versioned_ensembl_gene_id":"ENSG00000110619.17","gene_symbol":"CARS","gene_name":"cysteinyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:1493]","synonyms":"CARS1","biotype":"protein_coding","ncbi_id":"833","summary":"This gene encodes a class 1 aminoacyl-tRNA synthetase, cysteinyl-tRNA synthetase. Each of the twenty aminoacyl-tRNA synthetases catalyzes the aminoacylation of a specific tRNA or tRNA isoaccepting family with the cognate amino acid. This gene is one of several located near the imprinted gene domain on chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":3000922,"end":3057613,"strand":-1,"description":"cysteinyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:1493]"}, {"versioned_ensembl_gene_id":"ENSG00000242641.5","gene_symbol":"LINC00971","gene_name":"long intergenic non-protein coding RNA 971 [Source:HGNC Symbol;Acc:HGNC:48737]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440970","summary":null,"start":84638406,"end":84881679,"strand":-1,"description":"long intergenic non-protein coding RNA 971 [Source:HGNC Symbol;Acc:HGNC:48737]"}, {"versioned_ensembl_gene_id":"ENSG00000278707.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54521328,"end":54538122,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000241776.1","gene_symbol":"AC117482.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84691681,"end":84692591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127529.7","gene_symbol":"OR7C2","gene_name":"olfactory receptor family 7 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:8374]","synonyms":"OR7C3,OR19-18","biotype":"protein_coding","ncbi_id":"26658","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14941489,"end":14942448,"strand":1,"description":"olfactory receptor family 7 subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:8374]"}, {"versioned_ensembl_gene_id":"ENSG00000166947.11","gene_symbol":"EPB42","gene_name":"erythrocyte membrane protein band 4.2 [Source:HGNC Symbol;Acc:HGNC:3381]","synonyms":"PA,MGC116737,MGC116735","biotype":"protein_coding","ncbi_id":"2038","summary":"Erythrocyte membrane protein band 4.2 is an ATP-binding protein which may regulate the association of protein 3 with ankyrin. It probably has a role in erythrocyte shape and mechanical property regulation. Mutations in the EPB42 gene are associated with recessive spherocytic elliptocytosis and recessively transmitted hereditary hemolytic anemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":43106225,"end":43221283,"strand":-1,"description":"erythrocyte membrane protein band 4.2 [Source:HGNC Symbol;Acc:HGNC:3381]"}, {"versioned_ensembl_gene_id":"ENSG00000101850.12","gene_symbol":"GPR143","gene_name":"G protein-coupled receptor 143 [Source:HGNC Symbol;Acc:HGNC:20145]","synonyms":"OA1","biotype":"protein_coding","ncbi_id":"4935","summary":"This gene encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in this gene cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y. [provided by RefSeq, Dec 2009]","start":9725346,"end":9786297,"strand":-1,"description":"G protein-coupled receptor 143 [Source:HGNC Symbol;Acc:HGNC:20145]"}, {"versioned_ensembl_gene_id":"ENSG00000277227.1","gene_symbol":"AL359741.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28778224,"end":28778448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275867.3","gene_symbol":"KANSL1","gene_name":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]","synonyms":"MSL1v1,MSL1v1,KIAA1267,KIAA1267,DKFZP727C091,DKFZP727C091,CENP-36,CENP-36,NSL1,NSL1","biotype":"protein_coding","ncbi_id":"284058","summary":"This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes. [provided by RefSeq, Jun 2012]","start":45871009,"end":46068204,"strand":1,"description":"KAT8 regulatory NSL complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24565]"}, {"versioned_ensembl_gene_id":"ENSG00000233489.1","gene_symbol":"PAXBP1P1","gene_name":"PAX3 and PAX7 binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481704","summary":null,"start":153449429,"end":153449875,"strand":1,"description":"PAX3 and PAX7 binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50352]"}, {"versioned_ensembl_gene_id":"ENSG00000224316.1","gene_symbol":"GTF2IP5","gene_name":"general transcription factor IIi pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51717]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420546","summary":null,"start":65773620,"end":65802067,"strand":1,"description":"general transcription factor IIi pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:51717]"}, {"versioned_ensembl_gene_id":"ENSG00000284746.1","gene_symbol":"AC068587.10","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":12601158,"end":12601376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116898.11","gene_symbol":"MRPS15","gene_name":"mitochondrial ribosomal protein S15 [Source:HGNC Symbol;Acc:HGNC:14504]","synonyms":"FLJ11564","biotype":"protein_coding","ncbi_id":"64960","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S15P family. The encoded protein is more than two times the size of its E. coli counterpart, with the 12S rRNA binding sites conserved. Between human and mouse, the encoded protein is the least conserved among small subunit ribosomal proteins. Pseudogenes corresponding to this gene are found on chromosomes 15q and 19q. [provided by RefSeq, Jul 2008]","start":36455718,"end":36464437,"strand":-1,"description":"mitochondrial ribosomal protein S15 [Source:HGNC Symbol;Acc:HGNC:14504]"}, {"versioned_ensembl_gene_id":"ENSG00000205186.2","gene_symbol":"FABP9","gene_name":"fatty acid binding protein 9 [Source:HGNC Symbol;Acc:HGNC:3563]","synonyms":"T-FABP,PERF15,PERF","biotype":"protein_coding","ncbi_id":"646480","summary":null,"start":81458341,"end":81461579,"strand":-1,"description":"fatty acid binding protein 9 [Source:HGNC Symbol;Acc:HGNC:3563]"}, {"versioned_ensembl_gene_id":"ENSG00000228813.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32735261,"end":32742700,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000147588.6","gene_symbol":"PMP2","gene_name":"peripheral myelin protein 2 [Source:HGNC Symbol;Acc:HGNC:9117]","synonyms":"MP2,M-FABP,FABP8","biotype":"protein_coding","ncbi_id":"5375","summary":"The protein encoded by this gene localizes to myelin sheaths of the peripheral nervous system. The encoded protein can bind both the membrane layers of the sheaths and monomeric lipids, and is thought to provide stability to the sheath. A defect in this gene was shown to be a cause of dominant demyelinating CMT neuropathy. [provided by RefSeq, Jan 2017]","start":81440326,"end":81447523,"strand":-1,"description":"peripheral myelin protein 2 [Source:HGNC Symbol;Acc:HGNC:9117]"}, {"versioned_ensembl_gene_id":"ENSG00000281597.1","gene_symbol":"CR854858.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13115828,"end":13118626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225105.2","gene_symbol":"LINC01076","gene_name":"long intergenic non-protein coding RNA 1076 [Source:HGNC Symbol;Acc:HGNC:49119]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144602","summary":null,"start":25193107,"end":25210295,"strand":-1,"description":"long intergenic non-protein coding RNA 1076 [Source:HGNC Symbol;Acc:HGNC:49119]"}, {"versioned_ensembl_gene_id":"ENSG00000238267.1","gene_symbol":"AC104850.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39338129,"end":39338879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238169.1","gene_symbol":"LINC01053","gene_name":"long intergenic non-protein coding RNA 1053 [Source:HGNC Symbol;Acc:HGNC:49047]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723318","summary":null,"start":25181441,"end":25189760,"strand":1,"description":"long intergenic non-protein coding RNA 1053 [Source:HGNC Symbol;Acc:HGNC:49047]"}, {"versioned_ensembl_gene_id":"ENSG00000269893.6","gene_symbol":"SNHG8","gene_name":"small nucleolar RNA host gene 8 [Source:HGNC Symbol;Acc:HGNC:33098]","synonyms":"LINC00060,NCRNA00060","biotype":"lincRNA","ncbi_id":"100093630","summary":null,"start":118278709,"end":118279823,"strand":1,"description":"small nucleolar RNA host gene 8 [Source:HGNC Symbol;Acc:HGNC:33098]"}, {"versioned_ensembl_gene_id":"ENSG00000024048.10","gene_symbol":"UBR2","gene_name":"ubiquitin protein ligase E3 component n-recognin 2 [Source:HGNC Symbol;Acc:HGNC:21289]","synonyms":"KIAA0349,dJ392M17.3,C6orf133,bA49A4.1","biotype":"protein_coding","ncbi_id":"23304","summary":"This gene encodes an E3 ubiquitin ligase of the N-end rule proteolytic pathway that targets proteins with destabilizing N-terminal residues for polyubiquitylation and proteasome-mediated degradation. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":42564062,"end":42693504,"strand":1,"description":"ubiquitin protein ligase E3 component n-recognin 2 [Source:HGNC Symbol;Acc:HGNC:21289]"}, {"versioned_ensembl_gene_id":"ENSG00000243289.1","gene_symbol":"AGAP13P","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:23499]","synonyms":"CTGLF9P,bA548K23.1","biotype":"unprocessed_pseudogene","ncbi_id":"728005","summary":null,"start":46816516,"end":46832476,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:23499]"}, {"versioned_ensembl_gene_id":"ENSG00000257596.1","gene_symbol":"AC078778.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54262615,"end":54279063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198218.10","gene_symbol":"QRICH1","gene_name":"glutamine rich 1 [Source:HGNC Symbol;Acc:HGNC:24713]","synonyms":"FLJ20259","biotype":"protein_coding","ncbi_id":"54870","summary":null,"start":49029707,"end":49094363,"strand":-1,"description":"glutamine rich 1 [Source:HGNC Symbol;Acc:HGNC:24713]"}, {"versioned_ensembl_gene_id":"ENSG00000228353.1","gene_symbol":"AL450322.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3767915,"end":3768751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249481.6","gene_symbol":"SPATS1","gene_name":"spermatogenesis associated serine rich 1 [Source:HGNC Symbol;Acc:HGNC:22957]","synonyms":"SRSP1,SPATA8,FLJ25442","biotype":"protein_coding","ncbi_id":"221409","summary":null,"start":44342660,"end":44377167,"strand":1,"description":"spermatogenesis associated serine rich 1 [Source:HGNC Symbol;Acc:HGNC:22957]"}, {"versioned_ensembl_gene_id":"ENSG00000159352.15","gene_symbol":"PSMD4","gene_name":"proteasome 26S subunit, non-ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9561]","synonyms":"S5A,Rpn10,AF-1,AF","biotype":"protein_coding","ncbi_id":"5710","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the non-ATPase subunits of the 19S regulator lid. Pseudogenes have been identified on chromosomes 10 and 21. [provided by RefSeq, Jul 2008]","start":151254703,"end":151267479,"strand":1,"description":"proteasome 26S subunit, non-ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9561]"}, {"versioned_ensembl_gene_id":"ENSG00000232712.6","gene_symbol":"KIZ-AS1","gene_name":"KIZ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51231]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929591","summary":null,"start":21154023,"end":21218289,"strand":-1,"description":"KIZ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51231]"}, {"versioned_ensembl_gene_id":"ENSG00000279091.1","gene_symbol":"AC026523.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":97533738,"end":97541476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279830.1","gene_symbol":"NDUFB9P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075233","summary":null,"start":69349947,"end":69350456,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52269]"}, {"versioned_ensembl_gene_id":"ENSG00000264269.1","gene_symbol":"AC016866.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49023703,"end":49048474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149929.15","gene_symbol":"HIRIP3","gene_name":"HIRA interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:4917]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8479","summary":"The HIRA protein shares sequence similarity with Hir1p and Hir2p, the two corepressors of histone gene transcription characterized in the yeast, Saccharomyces cerevisiae. The structural features of the HIRA protein suggest that it may function as part of a multiprotein complex. Several cDNAs encoding HIRA-interacting proteins, or HIRIPs, have been identified. In vitro, the protein encoded by this gene binds HIRA, as well as H2B and H3 core histones, indicating that a complex containing HIRA-HIRIP3 could function in some aspects of chromatin and histone metabolism. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[provided by RefSeq, Aug 2011]","start":29992321,"end":29996436,"strand":-1,"description":"HIRA interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:4917]"}, {"versioned_ensembl_gene_id":"ENSG00000123983.13","gene_symbol":"ACSL3","gene_name":"acyl-CoA synthetase long chain family member 3 [Source:HGNC Symbol;Acc:HGNC:3570]","synonyms":"PRO2194,FACL3,ACS3","biotype":"protein_coding","ncbi_id":"2181","summary":"The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in brain, and preferentially utilizes myristate, arachidonate, and eicosapentaenoate as substrates. The amino acid sequence of this isozyme is 92% identical to that of rat homolog. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":222860934,"end":222944639,"strand":1,"description":"acyl-CoA synthetase long chain family member 3 [Source:HGNC Symbol;Acc:HGNC:3570]"}, {"versioned_ensembl_gene_id":"ENSG00000235012.1","gene_symbol":"AF121897.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39525583,"end":39529855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206075.13","gene_symbol":"SERPINB5","gene_name":"serpin family B member 5 [Source:HGNC Symbol;Acc:HGNC:8949]","synonyms":"maspin,PI5","biotype":"protein_coding","ncbi_id":"5268","summary":null,"start":63476761,"end":63505085,"strand":1,"description":"serpin family B member 5 [Source:HGNC Symbol;Acc:HGNC:8949]"}, {"versioned_ensembl_gene_id":"ENSG00000275494.1","gene_symbol":"AC133552.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":25106569,"end":25107102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274089.4","gene_symbol":"PRIMA1","gene_name":"proline rich membrane anchor 1 [Source:HGNC Symbol;Acc:HGNC:18319]","synonyms":"PRIMA","biotype":"protein_coding","ncbi_id":"145270","summary":"The product of this gene functions to organize acetylcholinesterase (AChE) into tetramers, and to anchor AChE at neural cell membranes. [provided by RefSeq, Nov 2008]","start":93718298,"end":93788481,"strand":-1,"description":"proline rich membrane anchor 1 [Source:HGNC Symbol;Acc:HGNC:18319]"}, {"versioned_ensembl_gene_id":"ENSG00000260448.5","gene_symbol":"LCMT1-AS1","gene_name":"LCMT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51177]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723510","summary":null,"start":25085592,"end":25111555,"strand":-1,"description":"LCMT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51177]"}, {"versioned_ensembl_gene_id":"ENSG00000100348.9","gene_symbol":"TXN2","gene_name":"thioredoxin 2 [Source:HGNC Symbol;Acc:HGNC:17772]","synonyms":"MT-TRX","biotype":"protein_coding","ncbi_id":"25828","summary":"This nuclear gene encodes a mitochondrial member of the thioredoxin family, a group of small multifunctional redox-active proteins. The encoded protein may play important roles in the regulation of the mitochondrial membrane potential and in protection against oxidant-induced apoptosis. [provided by RefSeq, Jul 2008]","start":36467036,"end":36482030,"strand":-1,"description":"thioredoxin 2 [Source:HGNC Symbol;Acc:HGNC:17772]"}, {"versioned_ensembl_gene_id":"ENSG00000235421.1","gene_symbol":"AC114501.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65525629,"end":65554744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231505.1","gene_symbol":"AC108868.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106521903,"end":106538079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262700.1","gene_symbol":"AC133552.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25093387,"end":25095255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276970.1","gene_symbol":"GU182358.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54754966,"end":54767314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257885.1","gene_symbol":"PHBP18","gene_name":"prohibitin pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51551]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390311","summary":null,"start":48168847,"end":48169659,"strand":-1,"description":"prohibitin pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:51551]"}, {"versioned_ensembl_gene_id":"ENSG00000275750.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,cl-42,nkat1,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769705,"end":54783961,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000257848.1","gene_symbol":"AC074029.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48171590,"end":48173353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230262.6","gene_symbol":"MIRLET7DHG","gene_name":"MIRLET7D host gene [Source:HGNC Symbol;Acc:HGNC:37186]","synonyms":null,"biotype":"lincRNA","ncbi_id":"158257","summary":null,"start":94176602,"end":94204568,"strand":-1,"description":"MIRLET7D host gene [Source:HGNC Symbol;Acc:HGNC:37186]"}, {"versioned_ensembl_gene_id":"ENSG00000178233.17","gene_symbol":"TMEM151B","gene_name":"transmembrane protein 151B [Source:HGNC Symbol;Acc:HGNC:21315]","synonyms":"TMEM193,C6orf137,bA444E17.5","biotype":"protein_coding","ncbi_id":"441151","summary":null,"start":44270466,"end":44307506,"strand":1,"description":"transmembrane protein 151B [Source:HGNC Symbol;Acc:HGNC:21315]"}, {"versioned_ensembl_gene_id":"ENSG00000147081.14","gene_symbol":"AKAP4","gene_name":"A-kinase anchoring protein 4 [Source:HGNC Symbol;Acc:HGNC:374]","synonyms":"AKAP82,p82,HI,hAKAP82,Fsc1,CT99","biotype":"protein_coding","ncbi_id":"8852","summary":"The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is localized to the sperm flagellum and may be involved in the regulation of sperm motility. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":50190768,"end":50201013,"strand":-1,"description":"A-kinase anchoring protein 4 [Source:HGNC Symbol;Acc:HGNC:374]"}, {"versioned_ensembl_gene_id":"ENSG00000142178.7","gene_symbol":"SIK1","gene_name":"salt inducible kinase 1 [Source:HGNC Symbol;Acc:HGNC:11142]","synonyms":"SNF1LK,msk","biotype":"protein_coding","ncbi_id":"150094","summary":"This gene encodes a serine/threonine protein kinase that contains a ubiquitin-associated (UBA) domain. The encoded protein is a member of the adenosine monophosphate-activated kinase (AMPK) subfamily of kinases that play a role in conserved signal transduction pathways. A mutation in this gene is associated with early infantile epileptic encephalopathy 30. [provided by RefSeq, Nov 2016]","start":43414515,"end":43427128,"strand":-1,"description":"salt inducible kinase 1 [Source:HGNC Symbol;Acc:HGNC:11142]"}, {"versioned_ensembl_gene_id":"ENSG00000258051.1","gene_symbol":"AC074029.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48160245,"end":48160878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275821.2","gene_symbol":"C7orf34","gene_name":"chromosome 7 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:21750]","synonyms":"CTM-1","biotype":"protein_coding","ncbi_id":"135927","summary":null,"start":143000530,"end":143002052,"strand":1,"description":"chromosome 7 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:21750]"}, {"versioned_ensembl_gene_id":"ENSG00000232001.1","gene_symbol":"AC108868.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":106543014,"end":106544297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174365.19","gene_symbol":"SNHG11","gene_name":"small nucleolar RNA host gene 11 [Source:HGNC Symbol;Acc:HGNC:25046]","synonyms":"LINC00101,C20orf198","biotype":"processed_transcript","ncbi_id":"128439","summary":"This gene is a member of the non-protein-coding multiple snoRNA host gene family. Two snoRNAs are derived from the introns of this host gene. Although many alternative splice variants have been observed, the gene is thought to have no protein-coding potential. [provided by RefSeq, Jul 2008]","start":38446578,"end":38450921,"strand":1,"description":"small nucleolar RNA host gene 11 [Source:HGNC Symbol;Acc:HGNC:25046]"}, {"versioned_ensembl_gene_id":"ENSG00000129864.6","gene_symbol":"VCY","gene_name":"variable charge, Y-linked [Source:HGNC Symbol;Acc:HGNC:12668]","synonyms":"VCY1A,VCY1,BPY1","biotype":"protein_coding","ncbi_id":"9084","summary":"The protein encoded by this gene is a member of a family of human VCX/Y genes. This gene family has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. Members of the VCX/Y family share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. VCX/Y genes encode small and highly charged proteins of unknown function. This gene encodes a small, positively charged protein. The presence of a putative bipartite nuclear localization signal suggests that this gene encodes a nuclear protein. The genome has two identical copies of this gene within a palindromic region; this record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":13985772,"end":13986513,"strand":-1,"description":"variable charge, Y-linked [Source:HGNC Symbol;Acc:HGNC:12668]"}, {"versioned_ensembl_gene_id":"ENSG00000204380.4","gene_symbol":"PKP4-AS1","gene_name":"PKP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52580]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129029","summary":null,"start":158658337,"end":158735002,"strand":-1,"description":"PKP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52580]"}, {"versioned_ensembl_gene_id":"ENSG00000228130.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SMT3H2P,dJ271M21,SUMO2P,SMT3Bp","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29635589,"end":29635872,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000240087.3","gene_symbol":"RPSAP12","gene_name":"ribosomal protein SA pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:6504]","synonyms":"LAMRP2,LAMRL2,LAMR1P12","biotype":"processed_pseudogene","ncbi_id":"387867","summary":null,"start":68552995,"end":68553882,"strand":-1,"description":"ribosomal protein SA pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:6504]"}, {"versioned_ensembl_gene_id":"ENSG00000144283.21","gene_symbol":"PKP4","gene_name":"plakophilin 4 [Source:HGNC Symbol;Acc:HGNC:9026]","synonyms":"p0071","biotype":"protein_coding","ncbi_id":"8502","summary":"Armadillo-like proteins are characterized by a series of armadillo repeats, first defined in the Drosophila 'armadillo' gene product, that are typically 42 to 45 amino acids in length. These proteins can be divided into subfamilies based on their number of repeats, their overall sequence similarity, and the dispersion of the repeats throughout their sequences. Members of the p120(ctn)/plakophilin subfamily of Armadillo-like proteins, including CTNND1, CTNND2, PKP1, PKP2, PKP4, and ARVCF. PKP4 may be a component of desmosomal plaque and other adhesion plaques and is thought to be involved in regulating junctional plaque organization and cadherin function. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2015]","start":158456964,"end":158682879,"strand":1,"description":"plakophilin 4 [Source:HGNC Symbol;Acc:HGNC:9026]"}, {"versioned_ensembl_gene_id":"ENSG00000264843.1","gene_symbol":"AP001180.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10704297,"end":10709599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280700.1","gene_symbol":"AC136687.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22453604,"end":22457549,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263952.5","gene_symbol":"AP005120.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10893617,"end":10908783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225964.5","gene_symbol":"NRIR","gene_name":"negative regulator of interferon response (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:51269]","synonyms":"lncRNA-CMPK2","biotype":"antisense_RNA","ncbi_id":"104326052","summary":"This gene is thought to produce a functional long non-coding RNA. This transcript may be a negative regulator of interferon response. [provided by RefSeq, Feb 2015]","start":6828514,"end":6840464,"strand":-1,"description":"negative regulator of interferon response (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:51269]"}, {"versioned_ensembl_gene_id":"ENSG00000214318.3","gene_symbol":"ATP5G1P6","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39509]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505704","summary":null,"start":63496989,"end":63497400,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39509]"}, {"versioned_ensembl_gene_id":"ENSG00000171517.5","gene_symbol":"LPAR3","gene_name":"lysophosphatidic acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:14298]","synonyms":"RP4-678I3,LPA3,LP-A3,HOFNH30,EDG7,Edg-7","biotype":"protein_coding","ncbi_id":"23566","summary":"This gene encodes a member of the G protein-coupled receptor family, as well as the EDG family of proteins. This protein functions as a cellular receptor for lysophosphatidic acid and mediates lysophosphatidic acid-evoked calcium mobilization. This receptor couples predominantly to G(q/11) alpha proteins. [provided by RefSeq, Jul 2008]","start":84811602,"end":84893213,"strand":-1,"description":"lysophosphatidic acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:14298]"}, {"versioned_ensembl_gene_id":"ENSG00000124164.15","gene_symbol":"VAPB","gene_name":"VAMP associated protein B and C [Source:HGNC Symbol;Acc:HGNC:12649]","synonyms":"VAP-C,VAP-B,ALS8","biotype":"protein_coding","ncbi_id":"9217","summary":"The protein encoded by this gene is a type IV membrane protein found in plasma and intracellular vesicle membranes. The encoded protein is found as a homodimer and as a heterodimer with VAPA. This protein also can interact with VAMP1 and VAMP2 and may be involved in vesicle trafficking. [provided by RefSeq, Jul 2008]","start":58389122,"end":58451101,"strand":1,"description":"VAMP associated protein B and C [Source:HGNC Symbol;Acc:HGNC:12649]"}, {"versioned_ensembl_gene_id":"ENSG00000237957.6","gene_symbol":"CT47A5","gene_name":"cancer/testis antigen family 47, member A5 [Source:HGNC Symbol;Acc:HGNC:33286]","synonyms":"CT47.5","biotype":"protein_coding","ncbi_id":"728072","summary":null,"start":120963026,"end":120966348,"strand":-1,"description":"cancer/testis antigen family 47, member A5 [Source:HGNC Symbol;Acc:HGNC:33286]"}, {"versioned_ensembl_gene_id":"ENSG00000234030.1","gene_symbol":"TMEM97P1","gene_name":"transmembrane protein 97 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39640]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873880","summary":null,"start":43783123,"end":43783573,"strand":1,"description":"transmembrane protein 97 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39640]"}, {"versioned_ensembl_gene_id":"ENSG00000253385.1","gene_symbol":"AP003696.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102854455,"end":102856075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067182.7","gene_symbol":"TNFRSF1A","gene_name":"TNF receptor superfamily member 1A [Source:HGNC Symbol;Acc:HGNC:11916]","synonyms":"TNF-R-I,TNF-R,CD120a,TNFR60,TNFR1,TNFAR,TNF-R55","biotype":"protein_coding","ncbi_id":"7132","summary":"This gene encodes a member of the TNF receptor superfamily of proteins. The encoded receptor is found in membrane-bound and soluble forms that interact with membrane-bound and soluble forms, respectively, of its ligand, tumor necrosis factor alpha. Binding of membrane-bound tumor necrosis factor alpha to the membrane-bound receptor induces receptor trimerization and activation, which plays a role in cell survival, apoptosis, and inflammation. Proteolytic processing of the encoded receptor results in release of the soluble form of the receptor, which can interact with free tumor necrosis factor alpha to inhibit inflammation. Mutations in this gene underlie tumor necrosis factor receptor-associated periodic syndrome (TRAPS), characterized by fever, abdominal pain and other features. Mutations in this gene may also be associated with multiple sclerosis in human patients. [provided by RefSeq, Sep 2016]","start":6328757,"end":6342114,"strand":-1,"description":"TNF receptor superfamily member 1A [Source:HGNC Symbol;Acc:HGNC:11916]"}, {"versioned_ensembl_gene_id":"ENSG00000269989.1","gene_symbol":"AC036176.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":63485601,"end":63486018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214199.3","gene_symbol":"EEF1A1P12","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:3195]","synonyms":"EEF1AL10","biotype":"processed_pseudogene","ncbi_id":"644604","summary":null,"start":106697331,"end":106698676,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:3195]"}, {"versioned_ensembl_gene_id":"ENSG00000274404.3","gene_symbol":"GOLGA6L22","gene_name":"golgin A6 family-like 22 [Source:HGNC Symbol;Acc:HGNC:50289]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440243","summary":null,"start":22461390,"end":22471066,"strand":1,"description":"golgin A6 family-like 22 [Source:HGNC Symbol;Acc:HGNC:50289]"}, {"versioned_ensembl_gene_id":"ENSG00000154864.11","gene_symbol":"PIEZO2","gene_name":"piezo type mechanosensitive ion channel component 2 [Source:HGNC Symbol;Acc:HGNC:26270]","synonyms":"HsT771,HsT748,FLJ34907,FLJ23403,FLJ23144,FAM38B2,FAM38B,C18orf58,C18orf30","biotype":"protein_coding","ncbi_id":"63895","summary":"The protein encoded by this gene contains more than thirty transmembrane domains and likely functions as part of mechanically-activated (MA) cation channels. These channels serve to connect mechanical forces to biological signals. The encoded protein quickly adapts MA currents in somatosensory neurons. Defects in this gene are a cause of type 5 distal arthrogryposis. Several alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Feb 2014]","start":10666483,"end":11148762,"strand":-1,"description":"piezo type mechanosensitive ion channel component 2 [Source:HGNC Symbol;Acc:HGNC:26270]"}, {"versioned_ensembl_gene_id":"ENSG00000230386.4","gene_symbol":"AC104057.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":65617077,"end":65619214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217275.2","gene_symbol":"AL031777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26202156,"end":26202654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277315.1","gene_symbol":"AL021879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7867327,"end":7867614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258344.1","gene_symbol":"AC078778.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":54276631,"end":54345083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100311.16","gene_symbol":"PDGFB","gene_name":"platelet derived growth factor subunit B [Source:HGNC Symbol;Acc:HGNC:8800]","synonyms":"SSV,SIS","biotype":"protein_coding","ncbi_id":"5155","summary":"This gene encodes a member of the protein family comprised of both platelet-derived growth factors (PDGF) and vascular endothelial growth factors (VEGF). The encoded preproprotein is proteolytically processed to generate platelet-derived growth factor subunit B, which can homodimerize, or alternatively, heterodimerize with the related platelet-derived growth factor subunit A. These proteins bind and activate PDGF receptor tyrosine kinases, which play a role in a wide range of developmental processes. Mutations in this gene are associated with meningioma. Reciprocal translocations between chromosomes 22 and 17, at sites where this gene and that for collagen type 1, alpha 1 are located, are associated with dermatofibrosarcoma protuberans, a rare skin tumor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":39223359,"end":39244751,"strand":-1,"description":"platelet derived growth factor subunit B [Source:HGNC Symbol;Acc:HGNC:8800]"}, {"versioned_ensembl_gene_id":"ENSG00000242329.1","gene_symbol":"AC007215.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12840804,"end":12841079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111481.9","gene_symbol":"COPZ1","gene_name":"coatomer protein complex subunit zeta 1 [Source:HGNC Symbol;Acc:HGNC:2243]","synonyms":"COPZ,CGI-120","biotype":"protein_coding","ncbi_id":"22818","summary":"This gene encodes a subunit of the cytoplasmic coatamer protein complex, which is involved in autophagy and intracellular protein trafficking. The coatomer protein complex is comprised of seven subunits and functions as the coat protein of coat protein complex (COP)I-vesicles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":54301202,"end":54351849,"strand":1,"description":"coatomer protein complex subunit zeta 1 [Source:HGNC Symbol;Acc:HGNC:2243]"}, {"versioned_ensembl_gene_id":"ENSG00000262055.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42137734,"end":42142850,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000276966.2","gene_symbol":"HIST1H4E","gene_name":"histone cluster 1 H4 family member e [Source:HGNC Symbol;Acc:HGNC:4790]","synonyms":"H4FJ,H4/j","biotype":"protein_coding","ncbi_id":"8367","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26204552,"end":26206038,"strand":1,"description":"histone cluster 1 H4 family member e [Source:HGNC Symbol;Acc:HGNC:4790]"}, {"versioned_ensembl_gene_id":"ENSG00000241352.3","gene_symbol":"AC007688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12850982,"end":12851740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129862.6","gene_symbol":"VCY1B","gene_name":"variable charge, Y-linked 1B [Source:HGNC Symbol;Acc:HGNC:31751]","synonyms":"BPY1B","biotype":"protein_coding","ncbi_id":"353513","summary":"The protein encoded by this gene is a member of a family of human VCX/Y genes. This gene family has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. Members of the VCX/Y family share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. VCX/Y genes encode small and highly charged proteins of unknown function. This gene encodes a small, positively charged protein. The presence of a putative bipartite nuclear localization signal suggests that this gene encodes a nuclear protein. The genome has two identical copies of this gene within a palindromic region; this record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":14056217,"end":14056958,"strand":1,"description":"variable charge, Y-linked 1B [Source:HGNC Symbol;Acc:HGNC:31751]"}, {"versioned_ensembl_gene_id":"ENSG00000224517.6","gene_symbol":"HTR2A-AS1","gene_name":"HTR2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40289]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874082","summary":null,"start":46852143,"end":46856299,"strand":1,"description":"HTR2A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40289]"}, {"versioned_ensembl_gene_id":"ENSG00000236849.5","gene_symbol":"LINC01474","gene_name":"long intergenic non-protein coding RNA 1474 [Source:HGNC Symbol;Acc:HGNC:51111]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927258","summary":null,"start":72871728,"end":72874109,"strand":-1,"description":"long intergenic non-protein coding RNA 1474 [Source:HGNC Symbol;Acc:HGNC:51111]"}, {"versioned_ensembl_gene_id":"ENSG00000217825.2","gene_symbol":"AC099552.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155196563,"end":155198455,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106153.12","gene_symbol":"CHCHD2","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21645]","synonyms":"C7orf17","biotype":"protein_coding","ncbi_id":"51142","summary":"The protein encoded by this gene belongs to a class of eukaryotic CX(9)C proteins characterized by four cysteine residues spaced ten amino acids apart from one another. These residues form disulfide linkages that define a CHCH fold. In response to stress, the protein translocates from the mitochondrial intermembrane space to the nucleus where it binds to a highly conserved 13 nucleotide oxygen responsive element in the promoter of cytochrome oxidase 4I2, a subunit of the terminal enzyme of the electron transport chain. In concert with recombination signal sequence-binding protein J, binding of this protein activates the oxygen responsive element at four percent oxygen. In addition, it has been shown that this protein is a negative regulator of mitochondria-mediated apoptosis. In response to apoptotic stimuli, mitochondrial levels of this protein decrease, allowing BCL2-associated X protein to oligomerize and activate the caspase cascade. Pseudogenes of this gene are found on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":56101569,"end":56106576,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21645]"}, {"versioned_ensembl_gene_id":"ENSG00000101323.4","gene_symbol":"HAO1","gene_name":"hydroxyacid oxidase 1 [Source:HGNC Symbol;Acc:HGNC:4809]","synonyms":"GOX1,GOX","biotype":"protein_coding","ncbi_id":"54363","summary":"This gene is one of three related genes that have 2-hydroxyacid oxidase activity yet differ in encoded protein amino acid sequence, tissue expression and substrate preference. Subcellular location of the encoded protein is the peroxisome. Specifically, this gene is expressed primarily in liver and pancreas and the encoded protein is most active on glycolate, a two-carbon substrate. The protein is also active on 2-hydroxy fatty acids. The transcript detected at high levels in pancreas may represent an alternatively spliced form or the use of a multiple near-consensus upstream polyadenylation site. [provided by RefSeq, Jul 2008]","start":7882981,"end":7940474,"strand":-1,"description":"hydroxyacid oxidase 1 [Source:HGNC Symbol;Acc:HGNC:4809]"}, {"versioned_ensembl_gene_id":"ENSG00000228042.2","gene_symbol":"AL512882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":110636841,"end":110637672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131931.8","gene_symbol":"THAP1","gene_name":"THAP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20856]","synonyms":"FLJ10477,DYT6,4833431A01Rik","biotype":"protein_coding","ncbi_id":"55145","summary":"The protein encoded by this gene contains a THAP domain, a conserved DNA-binding domain. This protein colocalizes with the apoptosis response protein PAWR/PAR-4 in promyelocytic leukemia (PML) nuclear bodies, and functions as a proapoptotic factor that links PAWR to PML nuclear bodies. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":42836674,"end":42843325,"strand":-1,"description":"THAP domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20856]"}, {"versioned_ensembl_gene_id":"ENSG00000253677.1","gene_symbol":"UBE2HP1","gene_name":"ubiquitin conjugating enzyme E2 H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31079]","synonyms":"UBE2HP","biotype":"processed_pseudogene","ncbi_id":"646463","summary":null,"start":81254870,"end":81255229,"strand":1,"description":"ubiquitin conjugating enzyme E2 H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31079]"}, {"versioned_ensembl_gene_id":"ENSG00000273802.2","gene_symbol":"HIST1H2BG","gene_name":"histone cluster 1 H2B family member g [Source:HGNC Symbol;Acc:HGNC:4746]","synonyms":"H2BFA,H2B/a,H2B.1A","biotype":"protein_coding","ncbi_id":"8339","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. The protein has antibacterial and antifungal antimicrobial activity. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":26215159,"end":26216692,"strand":-1,"description":"histone cluster 1 H2B family member g [Source:HGNC Symbol;Acc:HGNC:4746]"}, {"versioned_ensembl_gene_id":"ENSG00000272425.1","gene_symbol":"AC009902.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81275399,"end":81277570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161970.12","gene_symbol":"RPL26","gene_name":"ribosomal protein L26 [Source:HGNC Symbol;Acc:HGNC:10327]","synonyms":"L26","biotype":"protein_coding","ncbi_id":"6154","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L24P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Mutations in this gene result in Diamond-Blackfan anemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":8377520,"end":8383213,"strand":-1,"description":"ribosomal protein L26 [Source:HGNC Symbol;Acc:HGNC:10327]"}, {"versioned_ensembl_gene_id":"ENSG00000248886.2","gene_symbol":"UGT2A3P7","gene_name":"UDP glucuronosyltransferase family 2 member A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39429]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422023","summary":null,"start":69517667,"end":69518400,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member A3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39429]"}, {"versioned_ensembl_gene_id":"ENSG00000275346.1","gene_symbol":"CHCHD2P2","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39586]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728324","summary":null,"start":69333861,"end":69334181,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39586]"}, {"versioned_ensembl_gene_id":"ENSG00000223422.1","gene_symbol":"AC007274.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7678899,"end":7681028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186825.5","gene_symbol":"C2orf27B","gene_name":"chromosome 2 open reading frame 27B [Source:HGNC Symbol;Acc:HGNC:33824]","synonyms":"MGC50273","biotype":"lincRNA","ncbi_id":"408029","summary":null,"start":131794961,"end":131801661,"strand":-1,"description":"chromosome 2 open reading frame 27B [Source:HGNC Symbol;Acc:HGNC:33824]"}, {"versioned_ensembl_gene_id":"ENSG00000236440.1","gene_symbol":"AC117947.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140683360,"end":140683888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272153.1","gene_symbol":"AL365330.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3785008,"end":3785538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250180.1","gene_symbol":"AC074344.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":159398533,"end":159401246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267414.1","gene_symbol":"AC120049.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44676927,"end":44679717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130764.9","gene_symbol":"LRRC47","gene_name":"leucine rich repeat containing 47 [Source:HGNC Symbol;Acc:HGNC:29207]","synonyms":"RP1-286D6.3,KIAA1185","biotype":"protein_coding","ncbi_id":"57470","summary":null,"start":3778558,"end":3796504,"strand":-1,"description":"leucine rich repeat containing 47 [Source:HGNC Symbol;Acc:HGNC:29207]"}, {"versioned_ensembl_gene_id":"ENSG00000234748.1","gene_symbol":"AL109913.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146537535,"end":146538048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258479.5","gene_symbol":"LINC00640","gene_name":"long intergenic non-protein coding RNA 640 [Source:HGNC Symbol;Acc:HGNC:44291]","synonyms":null,"biotype":"lincRNA","ncbi_id":"283553","summary":null,"start":51333393,"end":51365557,"strand":1,"description":"long intergenic non-protein coding RNA 640 [Source:HGNC Symbol;Acc:HGNC:44291]"}, {"versioned_ensembl_gene_id":"ENSG00000279262.1","gene_symbol":"AC010335.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18448275,"end":18448802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258955.1","gene_symbol":"LINC00519","gene_name":"long intergenic non-protein coding RNA 519 [Source:HGNC Symbol;Acc:HGNC:19838]","synonyms":"C14orf30","biotype":"lincRNA","ncbi_id":"161342","summary":null,"start":51304416,"end":51328386,"strand":-1,"description":"long intergenic non-protein coding RNA 519 [Source:HGNC Symbol;Acc:HGNC:19838]"}, {"versioned_ensembl_gene_id":"ENSG00000249025.1","gene_symbol":"ZNF519P4","gene_name":"zinc finger protein 519 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50788]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481981","summary":null,"start":393534,"end":393658,"strand":1,"description":"zinc finger protein 519 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:50788]"}, {"versioned_ensembl_gene_id":"ENSG00000241678.1","gene_symbol":"AC091564.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6685891,"end":6686369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125810.9","gene_symbol":"CD93","gene_name":"CD93 molecule [Source:HGNC Symbol;Acc:HGNC:15855]","synonyms":"MXRA4,ECSM3,dJ737E23.1,CDw93,C1qRP,C1QR1,C1qR(P)","biotype":"protein_coding","ncbi_id":"22918","summary":"The protein encoded by this gene is a cell-surface glycoprotein and type I membrane protein that was originally identified as a myeloid cell-specific marker. The encoded protein was once thought to be a receptor for C1q, but now is thought to instead be involved in intercellular adhesion and in the clearance of apoptotic cells. The intracellular cytoplasmic tail of this protein has been found to interact with moesin, a protein known to play a role in linking transmembrane proteins to the cytoskeleton and in the remodelling of the cytoskeleton. [provided by RefSeq, Jul 2008]","start":23079349,"end":23086340,"strand":-1,"description":"CD93 molecule [Source:HGNC Symbol;Acc:HGNC:15855]"}, {"versioned_ensembl_gene_id":"ENSG00000129625.12","gene_symbol":"REEP5","gene_name":"receptor accessory protein 5 [Source:HGNC Symbol;Acc:HGNC:30077]","synonyms":"Yip2e,TB2,DP1,D5S346,C5orf18","biotype":"protein_coding","ncbi_id":"7905","summary":null,"start":112876379,"end":112922539,"strand":-1,"description":"receptor accessory protein 5 [Source:HGNC Symbol;Acc:HGNC:30077]"}, {"versioned_ensembl_gene_id":"ENSG00000251648.2","gene_symbol":"AC008958.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65732973,"end":65733654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234646.6","gene_symbol":"AL049651.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":23031542,"end":23039236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273270.1","gene_symbol":"AC090114.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128524016,"end":128531069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283196.1","gene_symbol":"AC006453.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89542842,"end":89585652,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274948.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816448,"end":54830767,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000233261.3","gene_symbol":"FAM238A","gene_name":"family with sequence similarity 238 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17776]","synonyms":"NCRNA00264,LINC00264,C10orf50,bA128B16.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645528","summary":null,"start":26589865,"end":26594330,"strand":1,"description":"family with sequence similarity 238 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17776]"}, {"versioned_ensembl_gene_id":"ENSG00000273682.1","gene_symbol":"AC109583.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46918807,"end":46918935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272382.1","gene_symbol":"AC025171.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43033716,"end":43034635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277421.3","gene_symbol":"ZNF280B","gene_name":"zinc finger protein 280B [Source:HGNC Symbol;Acc:HGNC:23022]","synonyms":"ZNF632,ZNF279,SUHW2,5'OY11.1","biotype":"protein_coding","ncbi_id":"140883","summary":"The protein encoded by this gene is a transcription factor that upregulates expression of MDM2, which negatively regulates p53 expression. This gene is highly expressed in prostate cancer cells, which leads to a reduction in p53 levels and an increase in growth of the cancer cells. Several transcript variants have been found for this gene, but only one of them is protein-coding. [provided by RefSeq, Jan 2015]","start":22493526,"end":22518259,"strand":-1,"description":"zinc finger protein 280B [Source:HGNC Symbol;Acc:HGNC:23022]"}, {"versioned_ensembl_gene_id":"ENSG00000198835.3","gene_symbol":"GJC2","gene_name":"gap junction protein gamma 2 [Source:HGNC Symbol;Acc:HGNC:17494]","synonyms":"SPG44,GJA12,CX47,CX46.6","biotype":"protein_coding","ncbi_id":"57165","summary":"This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1. [provided by RefSeq, Jul 2008]","start":228149852,"end":228159826,"strand":1,"description":"gap junction protein gamma 2 [Source:HGNC Symbol;Acc:HGNC:17494]"}, {"versioned_ensembl_gene_id":"ENSG00000284695.1","gene_symbol":"AC108941.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69810780,"end":69847786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134077.15","gene_symbol":"THUMPD3","gene_name":"THUMP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24493]","synonyms":"DKFZP434F091","biotype":"protein_coding","ncbi_id":"25917","summary":null,"start":9362842,"end":9386791,"strand":1,"description":"THUMP domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24493]"}, {"versioned_ensembl_gene_id":"ENSG00000241556.1","gene_symbol":"AC018475.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95467397,"end":95467861,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230525.5","gene_symbol":"LINC01799","gene_name":"long intergenic non-protein coding RNA 1799 [Source:HGNC Symbol;Acc:HGNC:52589]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060019","summary":null,"start":66904436,"end":66971462,"strand":1,"description":"long intergenic non-protein coding RNA 1799 [Source:HGNC Symbol;Acc:HGNC:52589]"}, {"versioned_ensembl_gene_id":"ENSG00000234068.6","gene_symbol":"PAGE2","gene_name":"PAGE family member 2 [Source:HGNC Symbol;Acc:HGNC:31804]","synonyms":"MGC62094,GAGEC2,CT16.4,PAGE-2","biotype":"protein_coding","ncbi_id":"203569","summary":null,"start":55089008,"end":55092842,"strand":1,"description":"PAGE family member 2 [Source:HGNC Symbol;Acc:HGNC:31804]"}, {"versioned_ensembl_gene_id":"ENSG00000280941.1","gene_symbol":"IGLVI-38","gene_name":"immunoglobulin lambda variable (I)-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5935]","synonyms":"IGLV(I)-38","biotype":"IG_V_pseudogene","ncbi_id":"28768","summary":null,"start":22434907,"end":22435400,"strand":1,"description":"immunoglobulin lambda variable (I)-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5935]"}, {"versioned_ensembl_gene_id":"ENSG00000233163.1","gene_symbol":"RPS12P17","gene_name":"ribosomal protein S12 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35705]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271353","summary":null,"start":69161530,"end":69161906,"strand":-1,"description":"ribosomal protein S12 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:35705]"}, {"versioned_ensembl_gene_id":"ENSG00000198597.8","gene_symbol":"ZNF536","gene_name":"zinc finger protein 536 [Source:HGNC Symbol;Acc:HGNC:29025]","synonyms":"KIAA0390","biotype":"protein_coding","ncbi_id":"9745","summary":"The protein encoded by this gene is a highly conserved zinc finger protein. The encoded protein is most abundant in brain, where it negatively regulates neuronal differentiation. [provided by RefSeq, Sep 2015]","start":30228290,"end":30713538,"strand":1,"description":"zinc finger protein 536 [Source:HGNC Symbol;Acc:HGNC:29025]"}, {"versioned_ensembl_gene_id":"ENSG00000236917.1","gene_symbol":"DNAJA1P2","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39338]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131207","summary":null,"start":153761450,"end":153762646,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39338]"}, {"versioned_ensembl_gene_id":"ENSG00000227929.4","gene_symbol":"SRGAP3-AS3","gene_name":"SRGAP3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40900]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288831","summary":null,"start":9216895,"end":9219508,"strand":1,"description":"SRGAP3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:40900]"}, {"versioned_ensembl_gene_id":"ENSG00000282211.1","gene_symbol":"IGHV3-7","gene_name":"immunoglobulin heavy variable 3-7 [Source:HGNC Symbol;Acc:HGNC:5620]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28452","summary":null,"start":106062920,"end":106063454,"strand":-1,"description":"immunoglobulin heavy variable 3-7 [Source:HGNC Symbol;Acc:HGNC:5620]"}, {"versioned_ensembl_gene_id":"ENSG00000254396.1","gene_symbol":"AL355432.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27102630,"end":27104728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228450.2","gene_symbol":"AL049734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131492279,"end":131492886,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225118.1","gene_symbol":"AL392103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":92878092,"end":92878289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162591.15","gene_symbol":"MEGF6","gene_name":"multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]","synonyms":"EGFL3","biotype":"protein_coding","ncbi_id":"1953","summary":null,"start":3489920,"end":3611495,"strand":-1,"description":"multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]"}, {"versioned_ensembl_gene_id":"ENSG00000225479.1","gene_symbol":"PLCB1-IT1","gene_name":"PLCB1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41414]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874337","summary":null,"start":8248704,"end":8256918,"strand":1,"description":"PLCB1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41414]"}, {"versioned_ensembl_gene_id":"ENSG00000242610.1","gene_symbol":"OR5BH1P","gene_name":"olfactory receptor family 5 subfamily BH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15407]","synonyms":"OR5BH2P","biotype":"processed_pseudogene","ncbi_id":"81075","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":131398054,"end":131398972,"strand":-1,"description":"olfactory receptor family 5 subfamily BH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15407]"}, {"versioned_ensembl_gene_id":"ENSG00000116194.12","gene_symbol":"ANGPTL1","gene_name":"angiopoietin like 1 [Source:HGNC Symbol;Acc:HGNC:489]","synonyms":"ANG3,ARP1,AngY,ANGPT3","biotype":"protein_coding","ncbi_id":"9068","summary":"Angiopoietins are members of the vascular endothelial growth factor family and the only known growth factors largely specific for vascular endothelium. Angiopoietin-1, angiopoietin-2, and angiopoietin-4 participate in the formation of blood vessels. The protein encoded by this gene is another member of the angiopoietin family that is widely expressed in adult tissues with mRNA levels highest in highly vascularized tissues. This protein was found to be a secretory protein that does not act as an endothelial cell mitogen in vitro. [provided by RefSeq, Jul 2008]","start":178849705,"end":178871052,"strand":-1,"description":"angiopoietin like 1 [Source:HGNC Symbol;Acc:HGNC:489]"}, {"versioned_ensembl_gene_id":"ENSG00000275624.4","gene_symbol":"PRB3","gene_name":"proline rich protein BstNI subfamily 3 [Source:HGNC Symbol;Acc:HGNC:9339]","synonyms":"PRG","biotype":"protein_coding","ncbi_id":"5544","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Long\" allele. The protein isoforms encoded by this gene are recognized as the \"first line of oral defense\" against the detrimental effects of polyphenols in the diet and pathogen infections. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Nov 2015]","start":11262181,"end":11266062,"strand":-1,"description":"proline rich protein BstNI subfamily 3 [Source:HGNC Symbol;Acc:HGNC:9339]"}, {"versioned_ensembl_gene_id":"ENSG00000125733.17","gene_symbol":"TRIP10","gene_name":"thyroid hormone receptor interactor 10 [Source:HGNC Symbol;Acc:HGNC:12304]","synonyms":"STP,STOT,HSTP,CIP4","biotype":"protein_coding","ncbi_id":"9322","summary":null,"start":6737925,"end":6751526,"strand":1,"description":"thyroid hormone receptor interactor 10 [Source:HGNC Symbol;Acc:HGNC:12304]"}, {"versioned_ensembl_gene_id":"ENSG00000228196.1","gene_symbol":"PTPN2P1","gene_name":"protein tyrosine phosphatase, non-receptor type 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9653]","synonyms":"PTPTP1,PTPN2P","biotype":"processed_pseudogene","ncbi_id":"646981","summary":null,"start":178746683,"end":178747754,"strand":-1,"description":"protein tyrosine phosphatase, non-receptor type 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9653]"}, {"versioned_ensembl_gene_id":"ENSG00000147255.18","gene_symbol":"IGSF1","gene_name":"immunoglobulin superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:5948]","synonyms":"PGSF2,MGC75490,KIAA0364,INHBP,IGDC1,IGCD1","biotype":"protein_coding","ncbi_id":"3547","summary":"This gene encodes a member of the immunoglobulin-like domain-containing superfamily. Proteins in this superfamily contain varying numbers of immunoglobulin-like domains and are thought to participate in the regulation of interactions between cells. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]","start":131273506,"end":131578899,"strand":-1,"description":"immunoglobulin superfamily member 1 [Source:HGNC Symbol;Acc:HGNC:5948]"}, {"versioned_ensembl_gene_id":"ENSG00000251024.1","gene_symbol":"AC097372.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":146077846,"end":146108157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161082.12","gene_symbol":"CELF5","gene_name":"CUGBP Elav-like family member 5 [Source:HGNC Symbol;Acc:HGNC:14058]","synonyms":"BRUNOL5","biotype":"protein_coding","ncbi_id":"60680","summary":"This gene encodes a member of the the CELF/BRUNOL protein family, which contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing and translation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]","start":3224703,"end":3297076,"strand":1,"description":"CUGBP Elav-like family member 5 [Source:HGNC Symbol;Acc:HGNC:14058]"}, {"versioned_ensembl_gene_id":"ENSG00000232280.9","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30717565,"end":30732592,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000215168.2","gene_symbol":"AL139276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66055587,"end":66056587,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170782.3","gene_symbol":"OR10A4","gene_name":"olfactory receptor family 10 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:15130]","synonyms":"OR10A4P","biotype":"protein_coding","ncbi_id":"283297","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6876625,"end":6877619,"strand":1,"description":"olfactory receptor family 10 subfamily A member 4 [Source:HGNC Symbol;Acc:HGNC:15130]"}, {"versioned_ensembl_gene_id":"ENSG00000235325.1","gene_symbol":"AC009963.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107920763,"end":107921248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225814.1","gene_symbol":"GRPEL2P2","gene_name":"GrpE like 2, mitochondrial pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41970]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129994","summary":null,"start":64697878,"end":64698547,"strand":-1,"description":"GrpE like 2, mitochondrial pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:41970]"}, {"versioned_ensembl_gene_id":"ENSG00000198954.7","gene_symbol":"KIF1BP","gene_name":"KIF1 binding protein [Source:HGNC Symbol;Acc:HGNC:23419]","synonyms":"TTC20,KIAA1279,KBP,DKFZP586B0923","biotype":"protein_coding","ncbi_id":"26128","summary":"This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]","start":68988721,"end":69043544,"strand":1,"description":"KIF1 binding protein [Source:HGNC Symbol;Acc:HGNC:23419]"}, {"versioned_ensembl_gene_id":"ENSG00000282066.1","gene_symbol":"IGHVIII-5-1","gene_name":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]","synonyms":"IGHV(III)-5-1","biotype":"IG_V_pseudogene","ncbi_id":"28354","summary":null,"start":106040437,"end":106040535,"strand":-1,"description":"immunoglobulin heavy variable (III)-5-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5702]"}, {"versioned_ensembl_gene_id":"ENSG00000282213.1","gene_symbol":"IGHV1-3","gene_name":"immunoglobulin heavy variable 1-3 [Source:HGNC Symbol;Acc:HGNC:5552]","synonyms":"VI-3B","biotype":"IG_V_gene","ncbi_id":"28473","summary":null,"start":106005866,"end":106006345,"strand":-1,"description":"immunoglobulin heavy variable 1-3 [Source:HGNC Symbol;Acc:HGNC:5552]"}, {"versioned_ensembl_gene_id":"ENSG00000234776.4","gene_symbol":"C11orf94","gene_name":"chromosome 11 open reading frame 94 [Source:HGNC Symbol;Acc:HGNC:37213]","synonyms":null,"biotype":"protein_coding","ncbi_id":"143678","summary":null,"start":45906513,"end":45907282,"strand":-1,"description":"chromosome 11 open reading frame 94 [Source:HGNC Symbol;Acc:HGNC:37213]"}, {"versioned_ensembl_gene_id":"ENSG00000116213.15","gene_symbol":"WRAP73","gene_name":"WD repeat containing, antisense to TP73 [Source:HGNC Symbol;Acc:HGNC:12759]","synonyms":"WDR8","biotype":"protein_coding","ncbi_id":"49856","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Studies of the related mouse protein suggest that the encoded protein may play a role in the process of ossification. [provided by RefSeq, Mar 2009]","start":3630767,"end":3652761,"strand":-1,"description":"WD repeat containing, antisense to TP73 [Source:HGNC Symbol;Acc:HGNC:12759]"}, {"versioned_ensembl_gene_id":"ENSG00000249509.1","gene_symbol":"AC023886.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112515385,"end":112546881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282696.1","gene_symbol":"AC243913.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28557827,"end":28557979,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281144.1","gene_symbol":"AC225613.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46518953,"end":46520589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222033.1","gene_symbol":"LINC01124","gene_name":"long intergenic non-protein coding RNA 1124 [Source:HGNC Symbol;Acc:HGNC:49270]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440925","summary":null,"start":170712451,"end":170714567,"strand":-1,"description":"long intergenic non-protein coding RNA 1124 [Source:HGNC Symbol;Acc:HGNC:49270]"}, {"versioned_ensembl_gene_id":"ENSG00000100243.20","gene_symbol":"CYB5R3","gene_name":"cytochrome b5 reductase 3 [Source:HGNC Symbol;Acc:HGNC:2873]","synonyms":"DIA1","biotype":"protein_coding","ncbi_id":"1727","summary":"This gene encodes cytochrome b5 reductase, which includes a membrane-bound form in somatic cells (anchored in the endoplasmic reticulum, mitochondrial and other membranes) and a soluble form in erythrocytes. The membrane-bound form exists mainly on the cytoplasmic side of the endoplasmic reticulum and functions in desaturation and elongation of fatty acids, in cholesterol biosynthesis, and in drug metabolism. The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is involved in methemoglobin reduction. The membrane-bound form has both membrane-binding and catalytic domains, while the soluble form has only the catalytic domain. Alternate splicing results in multiple transcript variants. Mutations in this gene cause methemoglobinemias. [provided by RefSeq, Jan 2010]","start":42617840,"end":42649568,"strand":-1,"description":"cytochrome b5 reductase 3 [Source:HGNC Symbol;Acc:HGNC:2873]"}, {"versioned_ensembl_gene_id":"ENSG00000255498.1","gene_symbol":"AC068385.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45905941,"end":45906461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121653.11","gene_symbol":"MAPK8IP1","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6882]","synonyms":"PRKM8IP,JIP1,JIP-1,IB1","biotype":"protein_coding","ncbi_id":"9479","summary":"This gene encodes a regulator of the pancreatic beta-cell function. It is highly similar to JIP-1, a mouse protein known to be a regulator of c-Jun amino-terminal kinase (Mapk8). This protein has been shown to prevent MAPK8 mediated activation of transcription factors, and to decrease IL-1 beta and MAP kinase kinase 1 (MEKK1) induced apoptosis in pancreatic beta cells. This protein also functions as a DNA-binding transactivator of the glucose transporter GLUT2. RE1-silencing transcription factor (REST) is reported to repress the expression of this gene in insulin-secreting beta cells. This gene is found to be mutated in a type 2 diabetes family, and thus is thought to be a susceptibility gene for type 2 diabetes. [provided by RefSeq, May 2011]","start":45885651,"end":45906465,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:6882]"}, {"versioned_ensembl_gene_id":"ENSG00000249319.2","gene_symbol":"AC068533.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":66087761,"end":66152277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178809.11","gene_symbol":"TRIM73","gene_name":"tripartite motif containing 73 [Source:HGNC Symbol;Acc:HGNC:18162]","synonyms":"TRIM50B","biotype":"protein_coding","ncbi_id":"375593","summary":null,"start":75395063,"end":75410996,"strand":1,"description":"tripartite motif containing 73 [Source:HGNC Symbol;Acc:HGNC:18162]"}, {"versioned_ensembl_gene_id":"ENSG00000102290.22","gene_symbol":"PCDH11X","gene_name":"protocadherin 11 X-linked [Source:HGNC Symbol;Acc:HGNC:8656]","synonyms":"PCDH-X,PPP1R119,PCDHX,PCDH11","biotype":"protein_coding","ncbi_id":"27328","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":91779261,"end":92623230,"strand":1,"description":"protocadherin 11 X-linked [Source:HGNC Symbol;Acc:HGNC:8656]"}, {"versioned_ensembl_gene_id":"ENSG00000276468.5","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"protein_coding","ncbi_id":"554300","summary":null,"start":54852887,"end":54865626,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000234702.1","gene_symbol":"VDAC1P3","gene_name":"voltage dependent anion channel 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37478]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310838","summary":null,"start":91982655,"end":91983505,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37478]"}, {"versioned_ensembl_gene_id":"ENSG00000279757.1","gene_symbol":"AC132068.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":72973374,"end":72973832,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271009.3","gene_symbol":"AC116667.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73060245,"end":73062316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241143.1","gene_symbol":"RPL32P9","gene_name":"ribosomal protein L32 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35481]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100270992","summary":null,"start":150150538,"end":150150944,"strand":1,"description":"ribosomal protein L32 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:35481]"}, {"versioned_ensembl_gene_id":"ENSG00000281157.2","gene_symbol":"ARHGEF26-AS1","gene_name":"ARHGEF26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41048]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507524","summary":null,"start":154119686,"end":154121332,"strand":-1,"description":"ARHGEF26 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41048]"}, {"versioned_ensembl_gene_id":"ENSG00000115977.18","gene_symbol":"AAK1","gene_name":"AP2 associated kinase 1 [Source:HGNC Symbol;Acc:HGNC:19679]","synonyms":"KIAA1048,DKFZp686K16132","biotype":"protein_coding","ncbi_id":"22848","summary":"This gene encodes a member of the SNF1 subfamily of serine/threonine protein kinases. Adaptor-related protein complex 2 (AP-2 complexes) functions during receptor-mediated endocytosis to trigger clathrin assembly, interact with membrane-bound receptors, and recruit encodytic accessory factors. The encoded protein interacts with and phosphorylates a subunit of the AP-2 complex, which promotes binding of AP-2 to sorting signals found in membrane-bound receptors and subsequent receptor endocytosis. Its kinase activity is stimulated by clathrin. This kinase has been shown to play an important role in regulating the clathrin-mediated endocytosis of the rabies virus, facilitating infection. Inhibitors of this kinase are being studied as candidate therapeutics to disrupt the entry of viruses, including SARS-CoV-2, into target cells. It is also involved in positive regulation of Notch pathway signaling in mammals. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Aug 2020]","start":69457997,"end":69674349,"strand":-1,"description":"AP2 associated kinase 1 [Source:HGNC Symbol;Acc:HGNC:19679]"}, {"versioned_ensembl_gene_id":"ENSG00000229948.2","gene_symbol":"B3GALNT1P1","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51302]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128857","summary":null,"start":69597353,"end":69598951,"strand":1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51302]"}, {"versioned_ensembl_gene_id":"ENSG00000225871.2","gene_symbol":"AC245100.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148435105,"end":148436926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255390.1","gene_symbol":"AC091564.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6621451,"end":6622322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170915.8","gene_symbol":"PAQR8","gene_name":"progestin and adipoQ receptor family member 8 [Source:HGNC Symbol;Acc:HGNC:15708]","synonyms":"MPRB,LMPB1,C6orf33","biotype":"protein_coding","ncbi_id":"85315","summary":null,"start":52361421,"end":52407777,"strand":1,"description":"progestin and adipoQ receptor family member 8 [Source:HGNC Symbol;Acc:HGNC:15708]"}, {"versioned_ensembl_gene_id":"ENSG00000279543.1","gene_symbol":"AC129908.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37473330,"end":37473977,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255717.6","gene_symbol":"SNHG1","gene_name":"small nucleolar RNA host gene 1 [Source:HGNC Symbol;Acc:HGNC:32688]","synonyms":"lncRNA16,LINC00057,UHG,NCRNA00057","biotype":"processed_transcript","ncbi_id":"23642","summary":"This locus represents a small nucleolar RNA host gene that produces multiple alternatively spliced long non-coding RNAs. This gene is upregulated in cancers and is thought to act as promoter of cell proliferation. This transcript negatively regulates tumor suppressor genes such as tumor protein p53. Expression of this locus may be a marker of tumor progression. [provided by RefSeq, Dec 2017]","start":62851988,"end":62855914,"strand":-1,"description":"small nucleolar RNA host gene 1 [Source:HGNC Symbol;Acc:HGNC:32688]"}, {"versioned_ensembl_gene_id":"ENSG00000072832.14","gene_symbol":"CRMP1","gene_name":"collapsin response mediator protein 1 [Source:HGNC Symbol;Acc:HGNC:2365]","synonyms":"DRP-1,DPYSL1","biotype":"protein_coding","ncbi_id":"1400","summary":"This gene encodes a member of a family of cytosolic phosphoproteins expressed exclusively in the nervous system. The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collapse during neural development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":5748084,"end":5893058,"strand":-1,"description":"collapsin response mediator protein 1 [Source:HGNC Symbol;Acc:HGNC:2365]"}, {"versioned_ensembl_gene_id":"ENSG00000238125.1","gene_symbol":"SLC9A3P2","gene_name":"solute carrier family 9 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19325]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"128997","summary":null,"start":20652730,"end":20654750,"strand":1,"description":"solute carrier family 9 member 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19325]"}, {"versioned_ensembl_gene_id":"ENSG00000122694.15","gene_symbol":"GLIPR2","gene_name":"GLI pathogenesis related 2 [Source:HGNC Symbol;Acc:HGNC:18007]","synonyms":"GAPR-1,C9orf19","biotype":"protein_coding","ncbi_id":"152007","summary":null,"start":36136536,"end":36163913,"strand":1,"description":"GLI pathogenesis related 2 [Source:HGNC Symbol;Acc:HGNC:18007]"}, {"versioned_ensembl_gene_id":"ENSG00000120952.4","gene_symbol":"PRAMEF2","gene_name":"PRAME family member 2 [Source:HGNC Symbol;Acc:HGNC:28841]","synonyms":"FLJ43580","biotype":"protein_coding","ncbi_id":"65122","summary":null,"start":12857086,"end":12861909,"strand":1,"description":"PRAME family member 2 [Source:HGNC Symbol;Acc:HGNC:28841]"}, {"versioned_ensembl_gene_id":"ENSG00000158864.12","gene_symbol":"NDUFS2","gene_name":"NADH:ubiquinone oxidoreductase core subunit S2 [Source:HGNC Symbol;Acc:HGNC:7708]","synonyms":"CI-49","biotype":"protein_coding","ncbi_id":"4720","summary":"The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":161197104,"end":161214395,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit S2 [Source:HGNC Symbol;Acc:HGNC:7708]"}, {"versioned_ensembl_gene_id":"ENSG00000229238.3","gene_symbol":"PPP1R12BP1","gene_name":"protein phosphatase 1 regulatory subunit 12B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18498]","synonyms":"PPP1R12BPY1,PPP1R12BP","biotype":"unprocessed_pseudogene","ncbi_id":"360021","summary":null,"start":26277923,"end":26354418,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 12B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18498]"}, {"versioned_ensembl_gene_id":"ENSG00000266993.3","gene_symbol":"AL050343.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51793934,"end":51799154,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262067.1","gene_symbol":"AC120057.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7058934,"end":7059204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224329.2","gene_symbol":"LINC00297","gene_name":"long intergenic non-protein coding RNA 297 [Source:HGNC Symbol;Acc:HGNC:39210]","synonyms":"NCRNA00297","biotype":"lincRNA","ncbi_id":"100874059","summary":null,"start":29872613,"end":29888405,"strand":-1,"description":"long intergenic non-protein coding RNA 297 [Source:HGNC Symbol;Acc:HGNC:39210]"}, {"versioned_ensembl_gene_id":"ENSG00000236306.2","gene_symbol":"LINC01241","gene_name":"long intergenic non-protein coding RNA 1241 [Source:NCBI gene;Acc:101929582]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929582","summary":null,"start":25780056,"end":25812968,"strand":1,"description":"long intergenic non-protein coding RNA 1241 [Source:NCBI gene;Acc:101929582]"}, {"versioned_ensembl_gene_id":"ENSG00000166949.15","gene_symbol":"SMAD3","gene_name":"SMAD family member 3 [Source:HGNC Symbol;Acc:HGNC:6769]","synonyms":"MADH3,JV15-2,HsT17436","biotype":"protein_coding","ncbi_id":"4088","summary":"The SMAD family of proteins are a group of intracellular signal transducer proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. The SMAD3 protein functions in the transforming growth factor-beta signaling pathway, and transmits signals from the cell surface to the nucleus, regulating gene activity and cell proliferation. It also functions as a tumor suppressor. Mutations in this gene are associated with aneurysms-osteoarthritis syndrome and Loeys-Dietz Syndrome 3. [provided by RefSeq, Nov 2019]","start":67063763,"end":67195195,"strand":1,"description":"SMAD family member 3 [Source:HGNC Symbol;Acc:HGNC:6769]"}, {"versioned_ensembl_gene_id":"ENSG00000236258.1","gene_symbol":"TIMM8BP1","gene_name":"translocase of inner mitochondrial membrane 8B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39211]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874425","summary":null,"start":29865959,"end":29866169,"strand":-1,"description":"translocase of inner mitochondrial membrane 8B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39211]"}, {"versioned_ensembl_gene_id":"ENSG00000282027.1","gene_symbol":"AC025674.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57272990,"end":57278377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271793.1","gene_symbol":"AL589666.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":85557978,"end":85615234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205632.3","gene_symbol":"LINC01310","gene_name":"long intergenic non-protein coding RNA 1310 [Source:HGNC Symbol;Acc:HGNC:50501]","synonyms":"WI2-81516E3.1","biotype":"lincRNA","ncbi_id":"100128946","summary":null,"start":48866770,"end":48898386,"strand":1,"description":"long intergenic non-protein coding RNA 1310 [Source:HGNC Symbol;Acc:HGNC:50501]"}, {"versioned_ensembl_gene_id":"ENSG00000214019.2","gene_symbol":"AL034370.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44029332,"end":44030921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259926.1","gene_symbol":"AC007342.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53448748,"end":53449590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226806.1","gene_symbol":"AC011893.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135820191,"end":135823087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231357.1","gene_symbol":"AC006028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2835621,"end":2836022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205442.12","gene_symbol":"IZUMO3","gene_name":"IZUMO family member 3 [Source:HGNC Symbol;Acc:HGNC:31421]","synonyms":"C9orf134,bA20A20.1","biotype":"protein_coding","ncbi_id":"100129669","summary":null,"start":24542952,"end":24545946,"strand":-1,"description":"IZUMO family member 3 [Source:HGNC Symbol;Acc:HGNC:31421]"}, {"versioned_ensembl_gene_id":"ENSG00000262136.1","gene_symbol":"AC092115.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69727013,"end":69742563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239828.6","gene_symbol":"AC063944.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":107272611,"end":107421304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235302.9","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"G6D,MEGT1,C6orf23,Ly6-D,NG25","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31706117,"end":31708565,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000227166.1","gene_symbol":"STSP1","gene_name":"steroid sulfatase (microsomal) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11426]","synonyms":"STSP,STS-Y","biotype":"unprocessed_pseudogene","ncbi_id":"6803","summary":null,"start":15547216,"end":15593331,"strand":1,"description":"steroid sulfatase (microsomal) pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11426]"}, {"versioned_ensembl_gene_id":"ENSG00000225304.1","gene_symbol":"AC106901.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":204379095,"end":204379792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000201467.1","gene_symbol":"SNORA16","gene_name":"Small nucleolar RNA SNORA16B/SNORA16A family [Source:RFAM;Acc:RF00190]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":17044380,"end":17044511,"strand":-1,"description":"Small nucleolar RNA SNORA16B/SNORA16A family [Source:RFAM;Acc:RF00190]"}, {"versioned_ensembl_gene_id":"ENSG00000225269.2","gene_symbol":"LINC00705","gene_name":"long intergenic non-protein coding RNA 705 [Source:HGNC Symbol;Acc:HGNC:27874]","synonyms":null,"biotype":"lincRNA","ncbi_id":"338588","summary":null,"start":4655427,"end":4662419,"strand":1,"description":"long intergenic non-protein coding RNA 705 [Source:HGNC Symbol;Acc:HGNC:27874]"}, {"versioned_ensembl_gene_id":"ENSG00000237271.1","gene_symbol":"AC009498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":204228137,"end":204234985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241722.2","gene_symbol":"AC083795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111551854,"end":111552173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162976.12","gene_symbol":"PQLC3","gene_name":"PQ loop repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:28503]","synonyms":"MGC33602,C2orf22","biotype":"protein_coding","ncbi_id":"130814","summary":null,"start":11155198,"end":11178874,"strand":1,"description":"PQ loop repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:28503]"}, {"versioned_ensembl_gene_id":"ENSG00000223460.1","gene_symbol":"GAPDHP69","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:4147]","synonyms":"GAPDL14,GAPDHL14","biotype":"processed_pseudogene","ncbi_id":"2611","summary":null,"start":29306778,"end":29307785,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:4147]"}, {"versioned_ensembl_gene_id":"ENSG00000107105.14","gene_symbol":"ELAVL2","gene_name":"ELAV like RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3313]","synonyms":"HuB,HEL-N1","biotype":"protein_coding","ncbi_id":"1993","summary":"In humans, the ELAV like RNA binding protein gene family has four members (ELAVL1-4). ELAVL RNA binding proteins recognize AU-rich elements in the 3' UTRs of gene transcripts and thereby regulate gene expression post-transcriptionally. The protein encoded by this gene binds to several 3' UTRs, including its own and also that of FOS, ID, and POU5F1. This gene encodes ELAVL2 and, like ELAVL3 and ELAVL4, is expressed specifically in neurons and primarily localizes to the cytoplasm. This protein also forms a cytosolic complex with the normally nuclear-localized ELAVL1 protein. Alternative splicing of this gene results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Jul 2020]","start":23690104,"end":23826337,"strand":-1,"description":"ELAV like RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3313]"}, {"versioned_ensembl_gene_id":"ENSG00000139194.7","gene_symbol":"RBP5","gene_name":"retinol binding protein 5 [Source:HGNC Symbol;Acc:HGNC:15847]","synonyms":"CRBPIII","biotype":"protein_coding","ncbi_id":"83758","summary":"The protein encoded by this gene is a cellular retinol-binding protein expressed highly in kidney and liver. Down-regulation of the encoded protein in hepatocellular carcinoma was associated with large tumor size and poor patient survival rates. [provided by RefSeq, Jul 2016]","start":7123684,"end":7128942,"strand":-1,"description":"retinol binding protein 5 [Source:HGNC Symbol;Acc:HGNC:15847]"}, {"versioned_ensembl_gene_id":"ENSG00000273958.1","gene_symbol":"AC009560.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60593027,"end":60593460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213594.4","gene_symbol":"GAPDHP25","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37777]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391367","summary":null,"start":38285410,"end":38286410,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37777]"}, {"versioned_ensembl_gene_id":"ENSG00000224876.1","gene_symbol":"AL121901.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33214920,"end":33217067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196715.5","gene_symbol":"VKORC1L1","gene_name":"vitamin K epoxide reductase complex subunit 1 like 1 [Source:HGNC Symbol;Acc:HGNC:21492]","synonyms":null,"biotype":"protein_coding","ncbi_id":"154807","summary":"This gene encodes an enzyme important in the vitamin K cycle, which is involved in the carboxylation of glutamate residues present in vitamin K-dependent proteins. The encoded enzyme catalyzes the de-epoxidation of vitamin K 2,3-epoxide. Oxidative stress may upregulate expression of this gene and the encoded protein may protect cells and membrane proteins form oxidative damage. This gene and a related gene (Gene ID: 79001) may have arisen by gene duplication of an ancestral gene. [provided by RefSeq, Oct 2016]","start":65873267,"end":65959563,"strand":1,"description":"vitamin K epoxide reductase complex subunit 1 like 1 [Source:HGNC Symbol;Acc:HGNC:21492]"}, {"versioned_ensembl_gene_id":"ENSG00000236529.1","gene_symbol":"AC093582.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65840212,"end":65840596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245534.6","gene_symbol":"RORA-AS1","gene_name":"RORA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51410]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928784","summary":null,"start":60479178,"end":60630637,"strand":1,"description":"RORA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51410]"}, {"versioned_ensembl_gene_id":"ENSG00000175206.10","gene_symbol":"NPPA","gene_name":"natriuretic peptide A [Source:HGNC Symbol;Acc:HGNC:7939]","synonyms":"PND,ANP","biotype":"protein_coding","ncbi_id":"4878","summary":"The protein encoded by this gene belongs to the natriuretic peptide family. Natriuretic peptides are implicated in the control of extracellular fluid volume and electrolyte homeostasis. This protein is synthesized as a large precursor (containing a signal peptide), which is processed to release a peptide from the N-terminus with similarity to vasoactive peptide, cardiodilatin, and another peptide from the C-terminus with natriuretic-diuretic activity. Mutations in this gene have been associated with atrial fibrillation familial type 6. This gene is located adjacent to another member of the natriuretic family of peptides on chromosome 1. [provided by RefSeq, Oct 2015]","start":11845709,"end":11848345,"strand":-1,"description":"natriuretic peptide A [Source:HGNC Symbol;Acc:HGNC:7939]"}, {"versioned_ensembl_gene_id":"ENSG00000243129.2","gene_symbol":"AC023790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13021260,"end":13021606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282335.1","gene_symbol":"OR9P1P","gene_name":"olfactory receptor family 9 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15097]","synonyms":"OR9P2P","biotype":"unprocessed_pseudogene","ncbi_id":"81382","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":143108400,"end":143108767,"strand":-1,"description":"olfactory receptor family 9 subfamily P member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15097]"}, {"versioned_ensembl_gene_id":"ENSG00000160207.8","gene_symbol":"HSF2BP","gene_name":"heat shock transcription factor 2 binding protein [Source:HGNC Symbol;Acc:HGNC:5226]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11077","summary":"HSF2 binding protein (HSF2BP) associates with HSF2. The interaction occurs between the trimerization domain of HSF2 and the amino terminal hydrophilic region of HSF2BP that comprises two leucine zipper motifs. HSF2BP may therefore be involved in modulating HSF2 activation. [provided by RefSeq, Jul 2008]","start":43529192,"end":43659493,"strand":-1,"description":"heat shock transcription factor 2 binding protein [Source:HGNC Symbol;Acc:HGNC:5226]"}, {"versioned_ensembl_gene_id":"ENSG00000248538.6","gene_symbol":"AC022784.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9189011,"end":9202854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281229.1","gene_symbol":"CR854858.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13125206,"end":13126314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012171.19","gene_symbol":"SEMA3B","gene_name":"semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]","synonyms":"sema5,SemA,LUCA-1,semaV,SEMAA","biotype":"protein_coding","ncbi_id":"7869","summary":"The protein encoded by this gene belongs to the class-3 semaphorin/collapsin family, whose members function in growth cone guidance during neuronal development. This family member inhibits axonal extension and has been shown to act as a tumor suppressor by inducing apoptosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":50267558,"end":50277546,"strand":1,"description":"semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]"}, {"versioned_ensembl_gene_id":"ENSG00000130762.14","gene_symbol":"ARHGEF16","gene_name":"Rho guanine nucleotide exchange factor 16 [Source:HGNC Symbol;Acc:HGNC:15515]","synonyms":"NBR,GEF16","biotype":"protein_coding","ncbi_id":"27237","summary":"Although the specific function of this protein is not known yet, it is thought to be involved in protein-protein and protein-lipid interactions. [provided by RefSeq, Jul 2008]","start":3454426,"end":3481113,"strand":1,"description":"Rho guanine nucleotide exchange factor 16 [Source:HGNC Symbol;Acc:HGNC:15515]"}, {"versioned_ensembl_gene_id":"ENSG00000185390.2","gene_symbol":"FGF7P2","gene_name":"fibroblast growth factor 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17193]","synonyms":"FGF7L","biotype":"unprocessed_pseudogene","ncbi_id":"394217","summary":null,"start":13349265,"end":13350648,"strand":1,"description":"fibroblast growth factor 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17193]"}, {"versioned_ensembl_gene_id":"ENSG00000133110.14","gene_symbol":"POSTN","gene_name":"periostin [Source:HGNC Symbol;Acc:HGNC:16953]","synonyms":"PN,periostin,OSF-2","biotype":"protein_coding","ncbi_id":"10631","summary":"This gene encodes a secreted extracellular matrix protein that functions in tissue development and regeneration, including wound healing, and ventricular remodeling following myocardial infarction. The encoded protein binds to integrins to support adhesion and migration of epithelial cells. This protein plays a role in cancer stem cell maintenance and metastasis. Mice lacking this gene exhibit cardiac valve disease, and skeletal and dental defects. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":37562583,"end":37598844,"strand":-1,"description":"periostin [Source:HGNC Symbol;Acc:HGNC:16953]"}, {"versioned_ensembl_gene_id":"ENSG00000101938.14","gene_symbol":"CHRDL1","gene_name":"chordin like 1 [Source:HGNC Symbol;Acc:HGNC:29861]","synonyms":"NRLN1,MGC1,CHL","biotype":"protein_coding","ncbi_id":"91851","summary":"This gene encodes an antagonist of bone morphogenetic protein 4. The encoded protein may play a role in topographic retinotectal projection and in the regulation of retinal angiogenesis in response to hypoxia. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jan 2009]","start":110673856,"end":110795819,"strand":-1,"description":"chordin like 1 [Source:HGNC Symbol;Acc:HGNC:29861]"}, {"versioned_ensembl_gene_id":"ENSG00000267139.1","gene_symbol":"AC005262.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3118665,"end":3119304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250630.1","gene_symbol":"MTCO1P35","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52100]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075234","summary":null,"start":106900854,"end":106901081,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:52100]"}, {"versioned_ensembl_gene_id":"ENSG00000205871.5","gene_symbol":"AC068724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43115702,"end":43116493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165899.10","gene_symbol":"OTOGL","gene_name":"otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]","synonyms":"FLJ90579,C12orf64","biotype":"protein_coding","ncbi_id":"283310","summary":"The protein encoded by this gene belongs to the otogelin family. This gene is expressed in the inner ear of vertebrates with the highest level of expression seen at the embryonic stage and lowest in adult. Knockdown studies in zebrafish suggest that this gene is essential for normal inner ear function. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2012]","start":80209453,"end":80379090,"strand":1,"description":"otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]"}, {"versioned_ensembl_gene_id":"ENSG00000233611.3","gene_symbol":"AC019068.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":236167447,"end":236294927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279246.1","gene_symbol":"AP003108.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61352244,"end":61354477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101460.12","gene_symbol":"MAP1LC3A","gene_name":"microtubule associated protein 1 light chain 3 alpha [Source:HGNC Symbol;Acc:HGNC:6838]","synonyms":"LC3,ATG8E,MAP1BLC3,MAP1ALC3,LC3A","biotype":"protein_coding","ncbi_id":"84557","summary":"MAP1A and MAP1B are microtubule-associated proteins which mediate the physical interactions between microtubules and components of the cytoskeleton. MAP1A and MAP1B each consist of a heavy chain subunit and multiple light chain subunits. The protein encoded by this gene is one of the light chain subunits and can associate with either MAP1A or MAP1B. Two transcript variants encoding different isoforms have been found for this gene. The expression of variant 1 is suppressed in many tumor cell lines, suggesting that may be involved in carcinogenesis. [provided by RefSeq, Feb 2012]","start":34546854,"end":34560345,"strand":1,"description":"microtubule associated protein 1 light chain 3 alpha [Source:HGNC Symbol;Acc:HGNC:6838]"}, {"versioned_ensembl_gene_id":"ENSG00000155876.5","gene_symbol":"RRAGA","gene_name":"Ras related GTP binding A [Source:HGNC Symbol;Acc:HGNC:16963]","synonyms":"RAGA,FIP-1","biotype":"protein_coding","ncbi_id":"10670","summary":null,"start":19049395,"end":19050983,"strand":1,"description":"Ras related GTP binding A [Source:HGNC Symbol;Acc:HGNC:16963]"}, {"versioned_ensembl_gene_id":"ENSG00000182177.13","gene_symbol":"ASB18","gene_name":"ankyrin repeat and SOCS box containing 18 [Source:HGNC Symbol;Acc:HGNC:19770]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401036","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and a SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. [provided by RefSeq, Feb 2017]","start":236194872,"end":236264409,"strand":-1,"description":"ankyrin repeat and SOCS box containing 18 [Source:HGNC Symbol;Acc:HGNC:19770]"}, {"versioned_ensembl_gene_id":"ENSG00000112116.9","gene_symbol":"IL17F","gene_name":"interleukin 17F [Source:HGNC Symbol;Acc:HGNC:16404]","synonyms":"ML-1,IL-17F,ML1","biotype":"protein_coding","ncbi_id":"112744","summary":"The protein encoded by this gene is a cytokine that shares sequence similarity with IL17. This cytokine is expressed by activated T cells, and has been shown to stimulate the production of several other cytokines, including IL6, IL8, and CSF2/GM_CSF. This cytokine is also found to inhibit the angiogenesis of endothelial cells and induce endothelial cells to produce IL2, TGFB1/TGFB, and monocyte chemoattractant protein-1. [provided by RefSeq, Jul 2008]","start":52236681,"end":52244537,"strand":-1,"description":"interleukin 17F [Source:HGNC Symbol;Acc:HGNC:16404]"}, {"versioned_ensembl_gene_id":"ENSG00000215034.4","gene_symbol":"DSTNP4","gene_name":"destrin, actin depolymerizing factor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44548]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729454","summary":null,"start":39214199,"end":39214672,"strand":1,"description":"destrin, actin depolymerizing factor pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44548]"}, {"versioned_ensembl_gene_id":"ENSG00000270055.1","gene_symbol":"AC127502.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30487963,"end":30490313,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280635.1","gene_symbol":"PROP1","gene_name":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5626","summary":"This gene encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Expression occurs prior to and is required for expression of pou domain transcription factor 1, which is responsible for pituitary development and hormone expression. Mutations in this gene have been associated with combined pituitary hormone deficiency-2 as well as deficiencies in luteinizing hormone, follicle-stimulating hormone, growth hormone, prolactin, and thyroid-stimulating hormone. [provided by RefSeq, Sep 2011]","start":177996182,"end":177996994,"strand":-1,"description":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]"}, {"versioned_ensembl_gene_id":"ENSG00000276833.2","gene_symbol":"TAF15","gene_name":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]","synonyms":"TAF2N,RBP56,Npl3,hTAFII68","biotype":"protein_coding","ncbi_id":"8148","summary":"This gene encodes a member of the TET family of RNA-binding proteins. The encoded protein plays a role in RNA polymerase II gene transcription as a component of a distinct subset of multi-subunit transcription initiation factor TFIID complexes. Translocations involving this gene play a role in acute leukemia and extraskeletal myxoid chondrosarcoma, and mutations in this gene may play a role in amyotrophic lateral sclerosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":35809455,"end":35864615,"strand":1,"description":"TATA-box binding protein associated factor 15 [Source:HGNC Symbol;Acc:HGNC:11547]"}, {"versioned_ensembl_gene_id":"ENSG00000236680.1","gene_symbol":"AL356000.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19026892,"end":19028129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228351.1","gene_symbol":"AC018832.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8079322,"end":8112924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273271.1","gene_symbol":"AP000254.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31666728,"end":31667247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256043.2","gene_symbol":"CTSO","gene_name":"cathepsin O [Source:HGNC Symbol;Acc:HGNC:2542]","synonyms":"CTSO1","biotype":"protein_coding","ncbi_id":"1519","summary":"The protein encoded by the gene is a cysteine proteinase and a member of the papain superfamily. This proteolytic enzyme is involved in cellular protein degradation and turnover. The recombinant form of this enzyme was shown to degrade synthetic peptides typically used as substrates for cysteine proteinases and its proteolytic activity was abolished by an inhibitor of cyteine proteinase. [provided by RefSeq, Jul 2008]","start":155924118,"end":155953917,"strand":-1,"description":"cathepsin O [Source:HGNC Symbol;Acc:HGNC:2542]"}, {"versioned_ensembl_gene_id":"ENSG00000235628.1","gene_symbol":"TNR-IT1","gene_name":"TNR intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41391]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874256","summary":null,"start":175538775,"end":175556818,"strand":-1,"description":"TNR intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41391]"}, {"versioned_ensembl_gene_id":"ENSG00000256474.1","gene_symbol":"TRAV11","gene_name":"T-cell receptor alpha variable 11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12104]","synonyms":null,"biotype":"TR_V_pseudogene","ncbi_id":"28675","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21829539,"end":21830070,"strand":1,"description":"T-cell receptor alpha variable 11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12104]"}, {"versioned_ensembl_gene_id":"ENSG00000237685.1","gene_symbol":"AL139039.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10511036,"end":10514546,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103248.18","gene_symbol":"MTHFSD","gene_name":"methenyltetrahydrofolate synthetase domain containing [Source:HGNC Symbol;Acc:HGNC:25778]","synonyms":"FLJ12998","biotype":"protein_coding","ncbi_id":"64779","summary":null,"start":86530176,"end":86555235,"strand":-1,"description":"methenyltetrahydrofolate synthetase domain containing [Source:HGNC Symbol;Acc:HGNC:25778]"}, {"versioned_ensembl_gene_id":"ENSG00000235228.2","gene_symbol":"BX120007.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32492462,"end":32492557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230949.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33137325,"end":33137948,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000162385.10","gene_symbol":"MAGOH","gene_name":"mago homolog, exon junction complex core component [Source:HGNC Symbol;Acc:HGNC:6815]","synonyms":"MAGOHA,MAGOH1","biotype":"protein_coding","ncbi_id":"4116","summary":"Drosophila that have mutations in their mago nashi (grandchildless) gene produce progeny with defects in germplasm assembly and germline development. This gene encodes the mammalian mago nashi homolog. In mammals, mRNA expression is not limited to the germ plasm, but is expressed ubiquitously in adult tissues and can be induced by serum stimulation of quiescent fibroblasts. [provided by RefSeq, Jul 2008]","start":53226892,"end":53238610,"strand":-1,"description":"mago homolog, exon junction complex core component [Source:HGNC Symbol;Acc:HGNC:6815]"}, {"versioned_ensembl_gene_id":"ENSG00000139644.12","gene_symbol":"TMBIM6","gene_name":"transmembrane BAX inhibitor motif containing 6 [Source:HGNC Symbol;Acc:HGNC:11723]","synonyms":"TEGT,BI-1,BAXI1","biotype":"protein_coding","ncbi_id":"7009","summary":null,"start":49707725,"end":49764934,"strand":1,"description":"transmembrane BAX inhibitor motif containing 6 [Source:HGNC Symbol;Acc:HGNC:11723]"}, {"versioned_ensembl_gene_id":"ENSG00000233952.1","gene_symbol":"FTLP15","gene_name":"ferritin light chain pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:37965]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442304","summary":null,"start":45997540,"end":45998071,"strand":-1,"description":"ferritin light chain pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:37965]"}, {"versioned_ensembl_gene_id":"ENSG00000187191.14","gene_symbol":"DAZ3","gene_name":"deleted in azoospermia 3 [Source:HGNC Symbol;Acc:HGNC:15965]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57054","summary":"This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains one copy of the 10.8 kb repeat. [provided by RefSeq, Jul 2008]","start":24763069,"end":24813492,"strand":-1,"description":"deleted in azoospermia 3 [Source:HGNC Symbol;Acc:HGNC:15965]"}, {"versioned_ensembl_gene_id":"ENSG00000151465.13","gene_symbol":"CDC123","gene_name":"cell division cycle 123 [Source:HGNC Symbol;Acc:HGNC:16827]","synonyms":"D123,C10orf7","biotype":"protein_coding","ncbi_id":"8872","summary":null,"start":12195965,"end":12250589,"strand":1,"description":"cell division cycle 123 [Source:HGNC Symbol;Acc:HGNC:16827]"}, {"versioned_ensembl_gene_id":"ENSG00000123200.16","gene_symbol":"ZC3H13","gene_name":"zinc finger CCCH-type containing 13 [Source:HGNC Symbol;Acc:HGNC:20368]","synonyms":"KIAA0853,DKFZp434D1812","biotype":"protein_coding","ncbi_id":"23091","summary":null,"start":45954465,"end":46052759,"strand":-1,"description":"zinc finger CCCH-type containing 13 [Source:HGNC Symbol;Acc:HGNC:20368]"}, {"versioned_ensembl_gene_id":"ENSG00000163975.11","gene_symbol":"MELTF","gene_name":"melanotransferrin [Source:HGNC Symbol;Acc:HGNC:7037]","synonyms":"MTF1,MTf,MGC4856,MFI2,MAP97,FLJ38863,CD228","biotype":"protein_coding","ncbi_id":"4241","summary":"The protein encoded by this gene is a cell-surface glycoprotein found on melanoma cells. The protein shares sequence similarity and iron-binding properties with members of the transferrin superfamily. The importance of the iron binding function has not yet been identified. This gene resides in the same region of chromosome 3 as members of the transferrin superfamily. Alternative splicing results in two transcript variants. [provided by RefSeq, Jul 2008]","start":196988621,"end":197029816,"strand":-1,"description":"melanotransferrin [Source:HGNC Symbol;Acc:HGNC:7037]"}, {"versioned_ensembl_gene_id":"ENSG00000204709.4","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"C6orf100,dJ25J6.5","biotype":"lincRNA","ncbi_id":"729583","summary":null,"start":28943877,"end":28944537,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000128394.16","gene_symbol":"APOBEC3F","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3F [Source:HGNC Symbol;Acc:HGNC:17356]","synonyms":"KA6,BK150C2.4.MRNA,ARP8","biotype":"protein_coding","ncbi_id":"200316","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":39040604,"end":39053910,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3F [Source:HGNC Symbol;Acc:HGNC:17356]"}, {"versioned_ensembl_gene_id":"ENSG00000255664.1","gene_symbol":"ARL6IP1P1","gene_name":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23178]","synonyms":"ARL6IPP1","biotype":"processed_pseudogene","ncbi_id":"100288702","summary":null,"start":21649728,"end":21650337,"strand":-1,"description":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23178]"}, {"versioned_ensembl_gene_id":"ENSG00000241641.1","gene_symbol":"RPS23P6","gene_name":"ribosomal protein S23 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36511]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271367","summary":null,"start":12081237,"end":12081902,"strand":1,"description":"ribosomal protein S23 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36511]"}, {"versioned_ensembl_gene_id":"ENSG00000260601.1","gene_symbol":"AC131391.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12545482,"end":12546684,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260723.1","gene_symbol":"AC007598.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12372812,"end":12373899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261247.1","gene_symbol":"GOLGA8T","gene_name":"golgin A8 family member T [Source:HGNC Symbol;Acc:HGNC:44410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653075","summary":null,"start":30135149,"end":30145567,"strand":1,"description":"golgin A8 family member T [Source:HGNC Symbol;Acc:HGNC:44410]"}, {"versioned_ensembl_gene_id":"ENSG00000234036.4","gene_symbol":"TXNP6","gene_name":"thioredoxin pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"171560","summary":null,"start":76958860,"end":76959169,"strand":-1,"description":"thioredoxin pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49486]"}, {"versioned_ensembl_gene_id":"ENSG00000102316.16","gene_symbol":"MAGED2","gene_name":"MAGE family member D2 [Source:HGNC Symbol;Acc:HGNC:16353]","synonyms":"MAGE-D2,JCL-1,HCA10,BCG1,11B6,MGC8386,MAGED","biotype":"protein_coding","ncbi_id":"10916","summary":"This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked intellectual disability (XLID). Mutations in this gene cause a form of transient antenatal Bartter's syndrome. This gene may also be involved in several types of cancer, including breast cancer and melanoma. The protein encoded by this gene is progressively recruited from the cytoplasm to the nucleoplasm during the interphase and after nucleolar stress and is thus thought to play a role in cell cycle regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":54807599,"end":54816012,"strand":1,"description":"MAGE family member D2 [Source:HGNC Symbol;Acc:HGNC:16353]"}, {"versioned_ensembl_gene_id":"ENSG00000144045.13","gene_symbol":"DQX1","gene_name":"DEAQ-box RNA dependent ATPase 1 [Source:HGNC Symbol;Acc:HGNC:20410]","synonyms":"FLJ23757","biotype":"protein_coding","ncbi_id":"165545","summary":null,"start":74518131,"end":74526336,"strand":-1,"description":"DEAQ-box RNA dependent ATPase 1 [Source:HGNC Symbol;Acc:HGNC:20410]"}, {"versioned_ensembl_gene_id":"ENSG00000238129.5","gene_symbol":"AL121904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26188408,"end":26196891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235080.1","gene_symbol":"MTND5P23","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42285]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873261","summary":null,"start":131370421,"end":131372075,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42285]"}, {"versioned_ensembl_gene_id":"ENSG00000172524.12","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30125643,"end":30138271,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000048707.13","gene_symbol":"VPS13D","gene_name":"vacuolar protein sorting 13 homolog D [Source:HGNC Symbol;Acc:HGNC:23595]","synonyms":"FLJ10619,KIAA0453","biotype":"protein_coding","ncbi_id":"55187","summary":"This gene encodes a protein belonging to the vacuolar-protein-sorting-13 gene family. In yeast, vacuolar-protein-sorting-13 proteins are involved in trafficking of membrane proteins between the trans-Golgi network and the prevacuolar compartment. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode distinct isoforms. [provided by RefSeq, Jul 2008]","start":12230067,"end":12512047,"strand":1,"description":"vacuolar protein sorting 13 homolog D [Source:HGNC Symbol;Acc:HGNC:23595]"}, {"versioned_ensembl_gene_id":"ENSG00000093100.13","gene_symbol":"AC016026.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":17787652,"end":17811497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234719.8","gene_symbol":"NPIPB2","gene_name":"nuclear pore complex interacting protein family, member B2 [Source:HGNC Symbol;Acc:HGNC:37451]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729978","summary":null,"start":11927373,"end":11976643,"strand":-1,"description":"nuclear pore complex interacting protein family, member B2 [Source:HGNC Symbol;Acc:HGNC:37451]"}, {"versioned_ensembl_gene_id":"ENSG00000205927.4","gene_symbol":"OLIG2","gene_name":"oligodendrocyte transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:9398]","synonyms":"RACK17,PRKCBP2,OLIGO2,bHLHe19,BHLHB1","biotype":"protein_coding","ncbi_id":"10215","summary":"This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq, Jul 2008]","start":33025845,"end":33029196,"strand":1,"description":"oligodendrocyte transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:9398]"}, {"versioned_ensembl_gene_id":"ENSG00000261390.5","gene_symbol":"MAFTRR","gene_name":"MAF transcriptional regulator RNA [Source:HGNC Symbol;Acc:HGNC:51525]","synonyms":"linc-MAF-4","biotype":"lincRNA","ncbi_id":"102467146","summary":null,"start":79715232,"end":79770563,"strand":-1,"description":"MAF transcriptional regulator RNA [Source:HGNC Symbol;Acc:HGNC:51525]"}, {"versioned_ensembl_gene_id":"ENSG00000188039.13","gene_symbol":"NWD1","gene_name":"NACHT and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27619]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284434","summary":"The protein encoded by this gene is thought to be a cytosolic protein and predicted to contain a NACHT domain and multiple WD40 repeats. Increased expression of this gene was observed in some prostate cancer cell lines. Knocking down expression of this gene results in decreased androgen receptor protein levels, indicating that this gene may be important in modulating androgen receptor activity. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":16719976,"end":16817963,"strand":1,"description":"NACHT and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:27619]"}, {"versioned_ensembl_gene_id":"ENSG00000108961.13","gene_symbol":"RANGRF","gene_name":"RAN guanine nucleotide release factor [Source:HGNC Symbol;Acc:HGNC:17679]","synonyms":"RANGNRF,MOG1,HSPC236,HSPC165","biotype":"protein_coding","ncbi_id":"29098","summary":"This gene encodes a protein that has been shown to function as a guanine nucleotide release factor in mouse and to regulate the expression and function of the Nav1.5 cardiac sodium channel in human. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":8288497,"end":8290092,"strand":1,"description":"RAN guanine nucleotide release factor [Source:HGNC Symbol;Acc:HGNC:17679]"}, {"versioned_ensembl_gene_id":"ENSG00000230354.1","gene_symbol":"STK19B","gene_name":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]","synonyms":"STK19P,RP2,bPG116M5.10","biotype":"unprocessed_pseudogene","ncbi_id":"373159","summary":null,"start":32089713,"end":32090230,"strand":1,"description":"serine/threonine kinase 19B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21668]"}, {"versioned_ensembl_gene_id":"ENSG00000137397.18","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30092451,"end":30102654,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000261082.1","gene_symbol":"LINC01228","gene_name":"long intergenic non-protein coding RNA 1228 [Source:HGNC Symbol;Acc:HGNC:49681]","synonyms":"lincRNA-DYNLRB2-2","biotype":"lincRNA","ncbi_id":"104266962","summary":null,"start":79798050,"end":79827150,"strand":-1,"description":"long intergenic non-protein coding RNA 1228 [Source:HGNC Symbol;Acc:HGNC:49681]"}, {"versioned_ensembl_gene_id":"ENSG00000112679.14","gene_symbol":"DUSP22","gene_name":"dual specificity phosphatase 22 [Source:HGNC Symbol;Acc:HGNC:16077]","synonyms":"VHX,MKPX,JSP1,JKAP","biotype":"protein_coding","ncbi_id":"56940","summary":null,"start":291630,"end":351355,"strand":1,"description":"dual specificity phosphatase 22 [Source:HGNC Symbol;Acc:HGNC:16077]"}, {"versioned_ensembl_gene_id":"ENSG00000224982.3","gene_symbol":"TMEM233","gene_name":"transmembrane protein 233 [Source:HGNC Symbol;Acc:HGNC:37219]","synonyms":"IFITMD2","biotype":"protein_coding","ncbi_id":"387890","summary":null,"start":119593459,"end":119643066,"strand":1,"description":"transmembrane protein 233 [Source:HGNC Symbol;Acc:HGNC:37219]"}, {"versioned_ensembl_gene_id":"ENSG00000270772.1","gene_symbol":"AC099777.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57800056,"end":57801448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271676.1","gene_symbol":"AC104771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77112495,"end":77113458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225099.1","gene_symbol":"ATP6V1E1P1","gene_name":"ATPase H+ transporting V1 subunit E1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:859]","synonyms":"ATP6V1EP1,ATP6EP1","biotype":"processed_pseudogene","ncbi_id":"343515","summary":null,"start":42903232,"end":42903912,"strand":1,"description":"ATPase H+ transporting V1 subunit E1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:859]"}, {"versioned_ensembl_gene_id":"ENSG00000278846.2","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107765,"end":42108953,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000257732.1","gene_symbol":"AC089983.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":104262314,"end":104280722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178996.13","gene_symbol":"SNX18","gene_name":"sorting nexin 18 [Source:HGNC Symbol;Acc:HGNC:19245]","synonyms":"SNAG1,SH3PXD3B,SH3PX2","biotype":"protein_coding","ncbi_id":"112574","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a SH3 domain. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54517759,"end":54546585,"strand":1,"description":"sorting nexin 18 [Source:HGNC Symbol;Acc:HGNC:19245]"}, {"versioned_ensembl_gene_id":"ENSG00000103152.11","gene_symbol":"MPG","gene_name":"N-methylpurine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:7211]","synonyms":"MDG","biotype":"protein_coding","ncbi_id":"4350","summary":null,"start":77007,"end":85853,"strand":1,"description":"N-methylpurine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:7211]"}, {"versioned_ensembl_gene_id":"ENSG00000277365.3","gene_symbol":"NDUFA6","gene_name":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]","synonyms":"NADHB14,LYRM6,CI-B14,B14","biotype":"protein_coding","ncbi_id":"4700","summary":"This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016]","start":42085525,"end":42090955,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]"}, {"versioned_ensembl_gene_id":"ENSG00000143627.17","gene_symbol":"PKLR","gene_name":"pyruvate kinase, liver and RBC [Source:HGNC Symbol;Acc:HGNC:9020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5313","summary":"The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":155289839,"end":155301434,"strand":-1,"description":"pyruvate kinase, liver and RBC [Source:HGNC Symbol;Acc:HGNC:9020]"}, {"versioned_ensembl_gene_id":"ENSG00000134278.15","gene_symbol":"SPIRE1","gene_name":"spire type actin nucleation factor 1 [Source:HGNC Symbol;Acc:HGNC:30622]","synonyms":"spir-1,KIAA1135","biotype":"protein_coding","ncbi_id":"56907","summary":"Spire proteins, such as SPIRE1, are highly conserved between species. They belong to the family of Wiskott-Aldrich homology region-2 (WH2) proteins, which are involved in actin organization (Kerkhoff et al., 2001 [PubMed 11747823]).[supplied by OMIM, Mar 2008]","start":12446512,"end":12658134,"strand":-1,"description":"spire type actin nucleation factor 1 [Source:HGNC Symbol;Acc:HGNC:30622]"}, {"versioned_ensembl_gene_id":"ENSG00000230965.1","gene_symbol":"SNX18P13","gene_name":"sorting nexin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39621]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419042","summary":null,"start":13905960,"end":13906488,"strand":-1,"description":"sorting nexin 18 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39621]"}, {"versioned_ensembl_gene_id":"ENSG00000168209.4","gene_symbol":"DDIT4","gene_name":"DNA damage inducible transcript 4 [Source:HGNC Symbol;Acc:HGNC:24944]","synonyms":"RTP801,REDD1,REDD-1,FLJ20500,Dig2","biotype":"protein_coding","ncbi_id":"54541","summary":null,"start":72273920,"end":72276036,"strand":1,"description":"DNA damage inducible transcript 4 [Source:HGNC Symbol;Acc:HGNC:24944]"}, {"versioned_ensembl_gene_id":"ENSG00000135824.12","gene_symbol":"RGS8","gene_name":"regulator of G protein signaling 8 [Source:HGNC Symbol;Acc:HGNC:16810]","synonyms":"MGC119069,MGC119068,MGC119067","biotype":"protein_coding","ncbi_id":"85397","summary":"This gene is a member of the regulator of G protein signaling (RGS) family and encodes a protein with a single RGS domain. Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. They accelerate transit through the cycle of GTP binding and hydrolysis to GDP, thereby terminating signal transduction, but paradoxically, also accelerate receptor-stimulated activation. [provided by RefSeq, Jul 2008]","start":182641816,"end":182684576,"strand":-1,"description":"regulator of G protein signaling 8 [Source:HGNC Symbol;Acc:HGNC:16810]"}, {"versioned_ensembl_gene_id":"ENSG00000135124.14","gene_symbol":"P2RX4","gene_name":"purinergic receptor P2X 4 [Source:HGNC Symbol;Acc:HGNC:8535]","synonyms":"P2X4","biotype":"protein_coding","ncbi_id":"5025","summary":"The product of this gene belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel with high calcium permeability. The main pharmacological distinction between the members of the purinoceptor family is the relative sensitivity to the antagonists suramin and PPADS. The product of this gene has the lowest sensitivity for these antagonists. Multiple alternatively spliced transcript variants, some protein-coding and some not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]","start":121209857,"end":121234106,"strand":1,"description":"purinergic receptor P2X 4 [Source:HGNC Symbol;Acc:HGNC:8535]"}, {"versioned_ensembl_gene_id":"ENSG00000224822.1","gene_symbol":"THRB-IT1","gene_name":"THRB intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41390]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874274","summary":null,"start":24455136,"end":24459434,"strand":-1,"description":"THRB intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41390]"}, {"versioned_ensembl_gene_id":"ENSG00000280556.1","gene_symbol":"BX247885.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42136436,"end":42139932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107443.15","gene_symbol":"CCNJ","gene_name":"cyclin J [Source:HGNC Symbol;Acc:HGNC:23434]","synonyms":"FLJ10895,bA690P14.1","biotype":"protein_coding","ncbi_id":"54619","summary":null,"start":96043394,"end":96060870,"strand":1,"description":"cyclin J [Source:HGNC Symbol;Acc:HGNC:23434]"}, {"versioned_ensembl_gene_id":"ENSG00000268884.1","gene_symbol":"AC010323.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8346517,"end":8347687,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278192.1","gene_symbol":"AL118505.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6065966,"end":6067897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240527.1","gene_symbol":"AL365273.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":95833508,"end":95873758,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281464.1","gene_symbol":"AC106795.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177870853,"end":177871194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145642.11","gene_symbol":"FAM159B","gene_name":"family with sequence similarity 159 member B [Source:HGNC Symbol;Acc:HGNC:34236]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132916","summary":null,"start":64690308,"end":64718090,"strand":1,"description":"family with sequence similarity 159 member B [Source:HGNC Symbol;Acc:HGNC:34236]"}, {"versioned_ensembl_gene_id":"ENSG00000259637.1","gene_symbol":"DNM1P38","gene_name":"dynamin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35188]","synonyms":"DNM1DN11-8,DNM1DN10@,DNM1DN10-2,DNM1P42,DNM1DN11@","biotype":"unprocessed_pseudogene","ncbi_id":"100216517","summary":null,"start":82531653,"end":82534139,"strand":-1,"description":"dynamin 1 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:35188]"}, {"versioned_ensembl_gene_id":"ENSG00000106341.10","gene_symbol":"PPP1R17","gene_name":"protein phosphatase 1 regulatory subunit 17 [Source:HGNC Symbol;Acc:HGNC:16973]","synonyms":"GSBS,C7orf16","biotype":"protein_coding","ncbi_id":"10842","summary":"The protein encoded by this gene is found primarily in cerebellar Purkinje cells, where it functions as a protein phosphatase inhibitor. The encoded protein is a substrate for cGMP-dependent protein kinase. An allele of this gene was discovered that increases susceptibility to hypercholesterolemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":31686715,"end":31708455,"strand":1,"description":"protein phosphatase 1 regulatory subunit 17 [Source:HGNC Symbol;Acc:HGNC:16973]"}, {"versioned_ensembl_gene_id":"ENSG00000254153.1","gene_symbol":"AC103957.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8456909,"end":8461337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268362.5","gene_symbol":"AC092279.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24033445,"end":24066909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136152.14","gene_symbol":"COG3","gene_name":"component of oligomeric golgi complex 3 [Source:HGNC Symbol;Acc:HGNC:18619]","synonyms":"SEC34","biotype":"protein_coding","ncbi_id":"83548","summary":"This gene encodes a component of the conserved oligomeric Golgi (COG) complex which is composed of eight different subunits and is required for normal Golgi morphology and localization. Defects in the COG complex result in multiple deficiencies in protein glycosylation. The protein encoded by this gene is involved in ER-Golgi transport.[provided by RefSeq, Jun 2011]","start":45464898,"end":45536630,"strand":1,"description":"component of oligomeric golgi complex 3 [Source:HGNC Symbol;Acc:HGNC:18619]"}, {"versioned_ensembl_gene_id":"ENSG00000253607.1","gene_symbol":"AC104316.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123002560,"end":123030751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261081.1","gene_symbol":"AC025678.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34409625,"end":34410594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273624.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":21428930,"end":21429036,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000197584.11","gene_symbol":"KCNMB2","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6286]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10242","summary":"MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit and the modulatory beta subunit. The protein encoded by this gene is an auxiliary beta subunit which decreases the activation time of MaxiK alpha subunit currents. Alternative splicing results in multiple transcript variants of this gene. Additional variants are discussed in the literature, but their full length nature has not been described. [provided by RefSeq, Jul 2013]","start":178272932,"end":178844429,"strand":1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:6286]"}, {"versioned_ensembl_gene_id":"ENSG00000271131.1","gene_symbol":"AC024220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178493327,"end":178493810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175877.3","gene_symbol":"TMEM270","gene_name":"transmembrane protein 270 [Source:HGNC Symbol;Acc:HGNC:23018]","synonyms":"WBSCR28,MGC26719","biotype":"protein_coding","ncbi_id":"135886","summary":null,"start":73861159,"end":73865893,"strand":1,"description":"transmembrane protein 270 [Source:HGNC Symbol;Acc:HGNC:23018]"}, {"versioned_ensembl_gene_id":"ENSG00000065717.14","gene_symbol":"TLE2","gene_name":"transducin like enhancer of split 2 [Source:HGNC Symbol;Acc:HGNC:11838]","synonyms":"FLJ41188,ESG2,ESG,GRG2","biotype":"protein_coding","ncbi_id":"7089","summary":null,"start":2997638,"end":3047635,"strand":-1,"description":"transducin like enhancer of split 2 [Source:HGNC Symbol;Acc:HGNC:11838]"}, {"versioned_ensembl_gene_id":"ENSG00000249388.1","gene_symbol":"AC023794.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54082118,"end":54102693,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125571.9","gene_symbol":"IL37","gene_name":"interleukin 37 [Source:HGNC Symbol;Acc:HGNC:15563]","synonyms":"IL1F7,IL-1RP1,IL-1H4,IL-1F7,FIL1Z,FIL1(ZETA),FIL1","biotype":"protein_coding","ncbi_id":"27178","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine can bind to, and may be a ligand for interleukin 18 receptor (IL18R1/IL-1Rrp). This cytokine also binds to interleukin 18 binding protein (IL18BP), an inhibitory binding protein of interleukin 18 (IL18), and subsequently forms a complex with IL18 receptor beta subunit, and through which it inhibits the activity of IL18. This gene along with eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. Five alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":112912971,"end":112918882,"strand":1,"description":"interleukin 37 [Source:HGNC Symbol;Acc:HGNC:15563]"}, {"versioned_ensembl_gene_id":"ENSG00000255032.1","gene_symbol":"AC104241.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44719392,"end":44736692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091651.8","gene_symbol":"ORC6","gene_name":"origin recognition complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:17151]","synonyms":"ORC6L","biotype":"protein_coding","ncbi_id":"23594","summary":"The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Gene silencing studies with small interfering RNA demonstrated that this protein plays an essential role in coordinating chromosome replication and segregation with cytokinesis. [provided by RefSeq, Oct 2010]","start":46689643,"end":46698394,"strand":1,"description":"origin recognition complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:17151]"}, {"versioned_ensembl_gene_id":"ENSG00000262141.1","gene_symbol":"AC040162.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":67855955,"end":67856111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168286.2","gene_symbol":"THAP11","gene_name":"THAP domain containing 11 [Source:HGNC Symbol;Acc:HGNC:23194]","synonyms":"HRIHFB2206,CTG-B45d,CTG-B43a","biotype":"protein_coding","ncbi_id":"57215","summary":"The protein encoded by this gene contains a THAP domain, which is a conserved DNA-binding domain that has striking similarity to the site-specific DNA-binding domain (DBD) of Drosophila P element transposases. [provided by RefSeq, Jul 2008]","start":67842082,"end":67844195,"strand":1,"description":"THAP domain containing 11 [Source:HGNC Symbol;Acc:HGNC:23194]"}, {"versioned_ensembl_gene_id":"ENSG00000226469.1","gene_symbol":"ADAM1B","gene_name":"ADAM metallopeptidase domain 1B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44366]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100420505","summary":null,"start":111927018,"end":111929017,"strand":1,"description":"ADAM metallopeptidase domain 1B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44366]"}, {"versioned_ensembl_gene_id":"ENSG00000280228.1","gene_symbol":"AC079753.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":112840328,"end":112844195,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262668.1","gene_symbol":"AJ003147.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3188212,"end":3224779,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088766.11","gene_symbol":"CRLS1","gene_name":"cardiolipin synthase 1 [Source:HGNC Symbol;Acc:HGNC:16148]","synonyms":"GCD10,dJ967N21.6,CLS1,C20orf155","biotype":"protein_coding","ncbi_id":"54675","summary":"This gene encodes a member of the CDP-alcohol phosphatidyltransferase class-I family of proteins. The encoded enzyme catalyzes the synthesis of cardiolipin, a phospholipid component of mitochondrial membranes that is critical for mitochondrial function. [provided by RefSeq, Apr 2016]","start":6006090,"end":6040053,"strand":1,"description":"cardiolipin synthase 1 [Source:HGNC Symbol;Acc:HGNC:16148]"}, {"versioned_ensembl_gene_id":"ENSG00000282313.1","gene_symbol":"AC239618.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":142936996,"end":142953930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218577.1","gene_symbol":"AL035696.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":167607,"end":170631,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228055.2","gene_symbol":"LINC00864","gene_name":"long intergenic non-protein coding RNA 864 [Source:HGNC Symbol;Acc:HGNC:45163]","synonyms":null,"biotype":"lincRNA","ncbi_id":"728218","summary":null,"start":87397023,"end":87424792,"strand":-1,"description":"long intergenic non-protein coding RNA 864 [Source:HGNC Symbol;Acc:HGNC:45163]"}, {"versioned_ensembl_gene_id":"ENSG00000225071.1","gene_symbol":"AC004552.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24429573,"end":24429920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236527.1","gene_symbol":"ARF4P2","gene_name":"ADP ribosylation factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16599]","synonyms":"dJ885L7.7","biotype":"processed_pseudogene","ncbi_id":"170485","summary":null,"start":62872250,"end":62873076,"strand":-1,"description":"ADP ribosylation factor 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16599]"}, {"versioned_ensembl_gene_id":"ENSG00000179381.7","gene_symbol":"OR4K11P","gene_name":"olfactory receptor family 4 subfamily K member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:15402]","synonyms":"OR21-1","biotype":"processed_pseudogene","ncbi_id":"81079","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":13544282,"end":13545185,"strand":-1,"description":"olfactory receptor family 4 subfamily K member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:15402]"}, {"versioned_ensembl_gene_id":"ENSG00000228380.1","gene_symbol":"MYL6BP1","gene_name":"myosin light chain 6B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422437","summary":null,"start":208269343,"end":208269957,"strand":-1,"description":"myosin light chain 6B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51647]"}, {"versioned_ensembl_gene_id":"ENSG00000111671.9","gene_symbol":"SPSB2","gene_name":"splA/ryanodine receptor domain and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:29522]","synonyms":"SSB-2,GRCC9","biotype":"protein_coding","ncbi_id":"84727","summary":"This gene encodes a member of a subfamily of proteins containing a central SPRY (repeats in splA and RyR) domain and a C-terminal suppressor of cytokine signaling (SOCS) box. This protein plays a role in cell signaling. This gene is present in a gene-rich cluster on chromosome 12p13 in the vicinity of the CD4 antigen and triosephosphate isomerase genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":6870935,"end":6889358,"strand":-1,"description":"splA/ryanodine receptor domain and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:29522]"}, {"versioned_ensembl_gene_id":"ENSG00000226782.2","gene_symbol":"AC117465.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177337628,"end":177349166,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250511.1","gene_symbol":"AC098798.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110512488,"end":110519505,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253238.1","gene_symbol":"AC104212.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80266154,"end":80339840,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164896.19","gene_symbol":"FASTK","gene_name":"Fas activated serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:24676]","synonyms":"FAST","biotype":"protein_coding","ncbi_id":"10922","summary":"The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase was shown to be activated rapidly during Fas-mediated apoptosis in Jurkat cells. In response to Fas receptor ligation, it phosphorylates TIA1, an apoptosis-promoting nuclear RNA-binding protein. The encoded protein is a strong inducer of lymphocyte apoptosis. Two transcript variants encoding different isoforms have been found for this gene. Other variants exist, but their full-length natures have not yet been determined. [provided by RefSeq, Jul 2008]","start":151076593,"end":151080866,"strand":-1,"description":"Fas activated serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:24676]"}, {"versioned_ensembl_gene_id":"ENSG00000221843.4","gene_symbol":"C2orf16","gene_name":"chromosome 2 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:25275]","synonyms":"DKFZp434G118","biotype":"protein_coding","ncbi_id":"84226","summary":null,"start":27537386,"end":27582721,"strand":1,"description":"chromosome 2 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:25275]"}, {"versioned_ensembl_gene_id":"ENSG00000255693.1","gene_symbol":"LINC02389","gene_name":"long intergenic non-protein coding RNA 2389 [Source:HGNC Symbol;Acc:HGNC:53316]","synonyms":"FLJ41278","biotype":"lincRNA","ncbi_id":"400046","summary":null,"start":64883394,"end":64977522,"strand":1,"description":"long intergenic non-protein coding RNA 2389 [Source:HGNC Symbol;Acc:HGNC:53316]"}, {"versioned_ensembl_gene_id":"ENSG00000253888.1","gene_symbol":"AC090150.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27184321,"end":27210494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258212.1","gene_symbol":"ZNF75BP","gene_name":"zinc finger protein 75B, pseudogene [Source:HGNC Symbol;Acc:HGNC:13147]","synonyms":"ZNF75B","biotype":"processed_pseudogene","ncbi_id":"7628","summary":null,"start":44008620,"end":44010143,"strand":-1,"description":"zinc finger protein 75B, pseudogene [Source:HGNC Symbol;Acc:HGNC:13147]"}, {"versioned_ensembl_gene_id":"ENSG00000257864.1","gene_symbol":"AC025030.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44248432,"end":44249004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245768.6","gene_symbol":"AC092378.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58733912,"end":59108974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271026.1","gene_symbol":"KATNBL1P1","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420919","summary":null,"start":28067587,"end":28068334,"strand":1,"description":"katanin regulatory subunit B1 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39724]"}, {"versioned_ensembl_gene_id":"ENSG00000101004.14","gene_symbol":"NINL","gene_name":"ninein like [Source:HGNC Symbol;Acc:HGNC:29163]","synonyms":"NLP,KIAA0980","biotype":"protein_coding","ncbi_id":"22981","summary":null,"start":25452705,"end":25585517,"strand":-1,"description":"ninein like [Source:HGNC Symbol;Acc:HGNC:29163]"}, {"versioned_ensembl_gene_id":"ENSG00000274979.1","gene_symbol":"AC020656.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":69326574,"end":69331882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089022.13","gene_symbol":"MAPKAPK5","gene_name":"mitogen-activated protein kinase-activated protein kinase 5 [Source:HGNC Symbol;Acc:HGNC:6889]","synonyms":"PRAK","biotype":"protein_coding","ncbi_id":"8550","summary":"The protein encoded by this gene is a tumor suppressor and member of the serine/threonine kinase family. In response to cellular stress and proinflammatory cytokines, this kinase is activated through its phosphorylation by MAP kinases including MAPK1/ERK, MAPK14/p38-alpha, and MAPK11/p38-beta. The encoded protein is found in the nucleus but translocates to the cytoplasm upon phosphorylation and activation. This kinase phosphorylates heat shock protein HSP27 at its physiologically relevant sites. Two alternately spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2012]","start":111841978,"end":111902238,"strand":1,"description":"mitogen-activated protein kinase-activated protein kinase 5 [Source:HGNC Symbol;Acc:HGNC:6889]"}, {"versioned_ensembl_gene_id":"ENSG00000205457.11","gene_symbol":"TP53TG3C","gene_name":"TP53 target 3C [Source:HGNC Symbol;Acc:HGNC:42962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653550","summary":null,"start":33193659,"end":33196858,"strand":1,"description":"TP53 target 3C [Source:HGNC Symbol;Acc:HGNC:42962]"}, {"versioned_ensembl_gene_id":"ENSG00000187715.13","gene_symbol":"KBTBD12","gene_name":"kelch repeat and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:25731]","synonyms":"FLJ46299,KLHDC6","biotype":"protein_coding","ncbi_id":"166348","summary":null,"start":127915232,"end":127987671,"strand":1,"description":"kelch repeat and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:25731]"}, {"versioned_ensembl_gene_id":"ENSG00000242001.1","gene_symbol":"AF186996.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125681305,"end":125681453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162929.13","gene_symbol":"KIAA1841","gene_name":"KIAA1841 [Source:HGNC Symbol;Acc:HGNC:29387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84542","summary":null,"start":61065871,"end":61138034,"strand":1,"description":"KIAA1841 [Source:HGNC Symbol;Acc:HGNC:29387]"}, {"versioned_ensembl_gene_id":"ENSG00000253903.2","gene_symbol":"AC090150.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27086076,"end":27087783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166960.16","gene_symbol":"CCDC178","gene_name":"coiled-coil domain containing 178 [Source:HGNC Symbol;Acc:HGNC:29588]","synonyms":"FLJ44050,C18orf34","biotype":"protein_coding","ncbi_id":"374864","summary":null,"start":32937402,"end":33441101,"strand":-1,"description":"coiled-coil domain containing 178 [Source:HGNC Symbol;Acc:HGNC:29588]"}, {"versioned_ensembl_gene_id":"ENSG00000224705.6","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ25550,Em:AB014087.1,FLJ31598","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30281062,"end":30317397,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000123364.4","gene_symbol":"HOXC13","gene_name":"homeobox C13 [Source:HGNC Symbol;Acc:HGNC:5125]","synonyms":"HOX3G,HOX3","biotype":"protein_coding","ncbi_id":"3229","summary":"This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the development of hair, nail, and filiform papilla. [provided by RefSeq, Jul 2008]","start":53938765,"end":53946544,"strand":1,"description":"homeobox C13 [Source:HGNC Symbol;Acc:HGNC:5125]"}, {"versioned_ensembl_gene_id":"ENSG00000274149.1","gene_symbol":"AC072046.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166605188,"end":166605455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243009.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"C6orf135,FLJ22638,Em:AB014085.3","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30319559,"end":30337137,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000157823.16","gene_symbol":"AP3S2","gene_name":"adaptor related protein complex 3 sigma 2 subunit [Source:HGNC Symbol;Acc:HGNC:571]","synonyms":"sigma3b","biotype":"protein_coding","ncbi_id":"10239","summary":null,"start":89830599,"end":89894638,"strand":-1,"description":"adaptor related protein complex 3 sigma 2 subunit [Source:HGNC Symbol;Acc:HGNC:571]"}, {"versioned_ensembl_gene_id":"ENSG00000155115.6","gene_symbol":"GTF3C6","gene_name":"general transcription factor IIIC subunit 6 [Source:HGNC Symbol;Acc:HGNC:20872]","synonyms":"TFIIIC35,C6orf51,bA397G5.3","biotype":"protein_coding","ncbi_id":"112495","summary":"RNA polymerases are unable to initiate RNA synthesis in the absence of additional proteins called general transcription factors (GTFs). GTFs assemble in a complex on the DNA promoter and recruit the RNA polymerase. GTF3C family proteins (e.g., GTF3C1, MIM 603246) are essential for RNA polymerase III to make a number of small nuclear and cytoplasmic RNAs, including 5S RNA (MIM 180420), tRNA, and adenovirus-associated (VA) RNA of both cellular and viral origin.[supplied by OMIM, Mar 2008]","start":110958560,"end":110967890,"strand":1,"description":"general transcription factor IIIC subunit 6 [Source:HGNC Symbol;Acc:HGNC:20872]"}, {"versioned_ensembl_gene_id":"ENSG00000250021.7","gene_symbol":"C15orf38-AP3S2","gene_name":"C15orf38-AP3S2 readthrough [Source:HGNC Symbol;Acc:HGNC:38824]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526783","summary":"This locus represents naturally occurring read-through transcription between the neighboring C15orf38 (chromosome 15 open reading frame 38) and AP3S2 (adaptor-related protein complex 3, sigma 2 subunit) genes. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":89834308,"end":89912882,"strand":-1,"description":"C15orf38-AP3S2 readthrough [Source:HGNC Symbol;Acc:HGNC:38824]"}, {"versioned_ensembl_gene_id":"ENSG00000214193.10","gene_symbol":"SH3D21","gene_name":"SH3 domain containing 21 [Source:HGNC Symbol;Acc:HGNC:26236]","synonyms":"FLJ22938,C1orf113","biotype":"protein_coding","ncbi_id":"79729","summary":null,"start":36306387,"end":36324886,"strand":1,"description":"SH3 domain containing 21 [Source:HGNC Symbol;Acc:HGNC:26236]"}, {"versioned_ensembl_gene_id":"ENSG00000279218.1","gene_symbol":"AC006037.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":234082259,"end":234084490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116670.14","gene_symbol":"MAD2L2","gene_name":"mitotic arrest deficient 2 like 2 [Source:HGNC Symbol;Acc:HGNC:6764]","synonyms":"REV7,POLZ2,MAD2B,FANCV","biotype":"protein_coding","ncbi_id":"10459","summary":"The protein encoded by this gene is a component of the mitotic spindle assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. The encoded protein, which is similar to MAD2L1, is capable of interacting with ADAM9, ADAM15, REV1, and REV3 proteins. [provided by RefSeq, Jul 2008]","start":11674480,"end":11691650,"strand":-1,"description":"mitotic arrest deficient 2 like 2 [Source:HGNC Symbol;Acc:HGNC:6764]"}, {"versioned_ensembl_gene_id":"ENSG00000225843.1","gene_symbol":"NIPA2P1","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42041]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132321","summary":null,"start":91320128,"end":91321103,"strand":-1,"description":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42041]"}, {"versioned_ensembl_gene_id":"ENSG00000236114.1","gene_symbol":"AL450326.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43523256,"end":43525217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253590.1","gene_symbol":"IGLV3-13","gene_name":"immunoglobulin lambda variable 3-13 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5899]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28801","summary":null,"start":22762294,"end":22762516,"strand":1,"description":"immunoglobulin lambda variable 3-13 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5899]"}, {"versioned_ensembl_gene_id":"ENSG00000256691.1","gene_symbol":"AC005908.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3462718,"end":3463586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244295.2","gene_symbol":"RPS20P21","gene_name":"ribosomal protein S20 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35993]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271234","summary":null,"start":73982125,"end":73982467,"strand":1,"description":"ribosomal protein S20 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35993]"}, {"versioned_ensembl_gene_id":"ENSG00000230575.1","gene_symbol":"AC013286.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76437408,"end":76438775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270891.1","gene_symbol":"AC012507.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":230836909,"end":230837385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254404.1","gene_symbol":"AP003306.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62213427,"end":62260549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224889.4","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30625856,"end":30626122,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000260511.1","gene_symbol":"AC009145.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79105957,"end":79110882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264217.2","gene_symbol":"RPL35AP25","gene_name":"ribosomal protein L35a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36294]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271633","summary":null,"start":45940522,"end":45940851,"strand":1,"description":"ribosomal protein L35a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36294]"}, {"versioned_ensembl_gene_id":"ENSG00000163029.15","gene_symbol":"SMC6","gene_name":"structural maintenance of chromosomes 6 [Source:HGNC Symbol;Acc:HGNC:20466]","synonyms":"FLJ22116,SMC6L1","biotype":"protein_coding","ncbi_id":"79677","summary":null,"start":17663812,"end":17800242,"strand":-1,"description":"structural maintenance of chromosomes 6 [Source:HGNC Symbol;Acc:HGNC:20466]"}, {"versioned_ensembl_gene_id":"ENSG00000247381.3","gene_symbol":"PLUT","gene_name":"PDX1 associated lncRNA, upregulator of transcription [Source:HGNC Symbol;Acc:HGNC:43698]","synonyms":"PLUTO,PDX1-AS1,HI-LNC71","biotype":"lincRNA","ncbi_id":"100861550","summary":null,"start":27819376,"end":27917298,"strand":-1,"description":"PDX1 associated lncRNA, upregulator of transcription [Source:HGNC Symbol;Acc:HGNC:43698]"}, {"versioned_ensembl_gene_id":"ENSG00000237746.1","gene_symbol":"ZNF101P1","gene_name":"zinc finger protein 101 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419867","summary":null,"start":28338554,"end":28340942,"strand":-1,"description":"zinc finger protein 101 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44940]"}, {"versioned_ensembl_gene_id":"ENSG00000147889.17","gene_symbol":"CDKN2A","gene_name":"cyclin dependent kinase inhibitor 2A [Source:HGNC Symbol;Acc:HGNC:1787]","synonyms":"INK4a,p19Arf,p19,INK4,p16INK4a,CMM2,p16,CDKN2,p14ARF,CDK4I,p14,ARF,MTS1,MLM","biotype":"protein_coding","ncbi_id":"1029","summary":"This gene generates several transcript variants which differ in their first exons. At least three alternatively spliced variants encoding distinct proteins have been reported, two of which encode structurally related isoforms known to function as inhibitors of CDK4 kinase. The remaining transcript includes an alternate first exon located 20 Kb upstream of the remainder of the gene; this transcript contains an alternate open reading frame (ARF) that specifies a protein which is structurally unrelated to the products of the other variants. This ARF product functions as a stabilizer of the tumor suppressor protein p53 as it can interact with, and sequester, the E3 ubiquitin-protein ligase MDM2, a protein responsible for the degradation of p53. In spite of the structural and functional differences, the CDK inhibitor isoforms and the ARF product encoded by this gene, through the regulatory roles of CDK4 and p53 in cell cycle G1 progression, share a common functionality in cell cycle G1 control. This gene is frequently mutated or deleted in a wide variety of tumors, and is known to be an important tumor suppressor gene. [provided by RefSeq, Sep 2012]","start":21967753,"end":21995301,"strand":-1,"description":"cyclin dependent kinase inhibitor 2A [Source:HGNC Symbol;Acc:HGNC:1787]"}, {"versioned_ensembl_gene_id":"ENSG00000112195.8","gene_symbol":"TREML2","gene_name":"triggering receptor expressed on myeloid cells like 2 [Source:HGNC Symbol;Acc:HGNC:21092]","synonyms":"TLT2,FLJ13693,dJ238O23.1,C6orf76","biotype":"protein_coding","ncbi_id":"79865","summary":"TREML2 is located in a gene cluster on chromosome 6 with the single Ig variable (IgV) domain activating receptors TREM1 (MIM 605085) and TREM2 (MIM 605086), but it has distinct structural and functional properties (Allcock et al., 2003 [PubMed 12645956]).[supplied by OMIM, Mar 2008]","start":41190277,"end":41201194,"strand":-1,"description":"triggering receptor expressed on myeloid cells like 2 [Source:HGNC Symbol;Acc:HGNC:21092]"}, {"versioned_ensembl_gene_id":"ENSG00000223600.1","gene_symbol":"EEF1A1P41","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:38799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874491","summary":null,"start":2995067,"end":2995273,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:38799]"}, {"versioned_ensembl_gene_id":"ENSG00000215874.3","gene_symbol":"CAPNS1P1","gene_name":"calpain small subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39562]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391053","summary":null,"start":89394033,"end":89394665,"strand":1,"description":"calpain small subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39562]"}, {"versioned_ensembl_gene_id":"ENSG00000277304.1","gene_symbol":"AC142086.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32916974,"end":32946392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114520.10","gene_symbol":"SNX4","gene_name":"sorting nexin 4 [Source:HGNC Symbol;Acc:HGNC:11175]","synonyms":"ATG24B","biotype":"protein_coding","ncbi_id":"8723","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein associated with the long isoform of the leptin receptor and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor in cell cultures, but its function is unknown. This protein may form oligomeric complexes with family members. Two transcript variants, one protein coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Nov 2012]","start":125446644,"end":125520197,"strand":-1,"description":"sorting nexin 4 [Source:HGNC Symbol;Acc:HGNC:11175]"}, {"versioned_ensembl_gene_id":"ENSG00000249105.2","gene_symbol":"AC096725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58117758,"end":58118070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219435.5","gene_symbol":"CATSPERZ","gene_name":"catsper channel auxiliary subunit zeta [Source:HGNC Symbol;Acc:HGNC:19231]","synonyms":"TEX40,DKFZP566E164,C11orf20","biotype":"protein_coding","ncbi_id":"25858","summary":null,"start":64300391,"end":64304770,"strand":1,"description":"catsper channel auxiliary subunit zeta [Source:HGNC Symbol;Acc:HGNC:19231]"}, {"versioned_ensembl_gene_id":"ENSG00000272205.1","gene_symbol":"AL451050.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":167219831,"end":167220512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253813.1","gene_symbol":"COX6B1P4","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:2284]","synonyms":"COX6BP4","biotype":"processed_pseudogene","ncbi_id":"100462850","summary":null,"start":26835817,"end":26836300,"strand":-1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:2284]"}, {"versioned_ensembl_gene_id":"ENSG00000240052.1","gene_symbol":"AC108114.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53413504,"end":53414260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227018.1","gene_symbol":"IL6STP1","gene_name":"interleukin 6 signal transducer pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6022]","synonyms":"IL6STP","biotype":"processed_pseudogene","ncbi_id":"3573","summary":null,"start":15783288,"end":15784307,"strand":1,"description":"interleukin 6 signal transducer pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6022]"}, {"versioned_ensembl_gene_id":"ENSG00000163964.14","gene_symbol":"PIGX","gene_name":"phosphatidylinositol glycan anchor biosynthesis class X [Source:HGNC Symbol;Acc:HGNC:26046]","synonyms":"FLJ20522","biotype":"protein_coding","ncbi_id":"54965","summary":"This gene encodes a type I transmembrane protein in the endoplasmic reticulum (ER). The protein is an essential component of glycosylphosphatidylinositol-mannosyltransferase I, which transfers the first of the four mannoses in the GPI-anchor precursors during GPI-anchor biosynthesis. Studies in rat indicate that the protein is translated from a non-AUG translation initiation site. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":196639775,"end":196736007,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class X [Source:HGNC Symbol;Acc:HGNC:26046]"}, {"versioned_ensembl_gene_id":"ENSG00000233367.1","gene_symbol":"AL133480.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6415145,"end":6449558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250333.1","gene_symbol":"AC093725.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57605694,"end":57658800,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234617.1","gene_symbol":"SNRK-AS1","gene_name":"SNRK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41269]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873954","summary":null,"start":43349644,"end":43351962,"strand":-1,"description":"SNRK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41269]"}, {"versioned_ensembl_gene_id":"ENSG00000075856.11","gene_symbol":"SART3","gene_name":"squamous cell carcinoma antigen recognized by T-cells 3 [Source:HGNC Symbol;Acc:HGNC:16860]","synonyms":"TIP110,RP11-13G14,p110,KIAA0156","biotype":"protein_coding","ncbi_id":"9733","summary":"The protein encoded by this gene is an RNA-binding nuclear protein that is a tumor-rejection antigen. This antigen possesses tumor epitopes capable of inducing HLA-A24-restricted and tumor-specific cytotoxic T lymphocytes in cancer patients and may be useful for specific immunotherapy. This gene product is found to be an important cellular factor for HIV-1 gene expression and viral replication. It also associates transiently with U6 and U4/U6 snRNPs during the recycling phase of the spliceosome cycle. This encoded protein is thought to be involved in the regulation of mRNA splicing. [provided by RefSeq, Jul 2008]","start":108522580,"end":108561400,"strand":-1,"description":"squamous cell carcinoma antigen recognized by T-cells 3 [Source:HGNC Symbol;Acc:HGNC:16860]"}, {"versioned_ensembl_gene_id":"ENSG00000227255.1","gene_symbol":"CDRT15P2","gene_name":"CMT1A duplicated region transcript 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34074]","synonyms":"CDRT15L1","biotype":"unprocessed_pseudogene","ncbi_id":"644694","summary":null,"start":15764703,"end":15765664,"strand":1,"description":"CMT1A duplicated region transcript 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34074]"}, {"versioned_ensembl_gene_id":"ENSG00000235922.1","gene_symbol":"AL354766.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46863563,"end":46864104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254223.1","gene_symbol":"AC103718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129679135,"end":129683679,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172428.10","gene_symbol":"COPS9","gene_name":"COP9 signalosome subunit 9 [Source:HGNC Symbol;Acc:HGNC:21314]","synonyms":"MYEOV2,CSNAP","biotype":"protein_coding","ncbi_id":"150678","summary":null,"start":240126563,"end":240136807,"strand":-1,"description":"COP9 signalosome subunit 9 [Source:HGNC Symbol;Acc:HGNC:21314]"}, {"versioned_ensembl_gene_id":"ENSG00000213854.3","gene_symbol":"CNN2P6","gene_name":"calponin 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339897","summary":null,"start":31181751,"end":31182650,"strand":-1,"description":"calponin 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39531]"}, {"versioned_ensembl_gene_id":"ENSG00000182504.10","gene_symbol":"CEP97","gene_name":"centrosomal protein 97 [Source:HGNC Symbol;Acc:HGNC:26244]","synonyms":"LRRIQ2,FLJ23047","biotype":"protein_coding","ncbi_id":"79598","summary":null,"start":101723925,"end":101770562,"strand":1,"description":"centrosomal protein 97 [Source:HGNC Symbol;Acc:HGNC:26244]"}, {"versioned_ensembl_gene_id":"ENSG00000071243.15","gene_symbol":"ING3","gene_name":"inhibitor of growth family member 3 [Source:HGNC Symbol;Acc:HGNC:14587]","synonyms":"p47ING3,MEAF4,FLJ20089,Eaf4","biotype":"protein_coding","ncbi_id":"54556","summary":"The protein encoded by this gene is similar to ING1, a tumor suppressor protein that can interact with TP53, inhibit cell growth, and induce apoptosis. This protein contains a PHD-finger, which is a common motif in proteins involved in chromatin remodeling. This gene can activate p53 trans-activated promoters, including promoters of p21/waf1 and bax. Overexpression of this gene has been shown to inhibit cell growth and induce apoptosis. Allelic loss and reduced expression of this gene were detected in head and neck cancers. Two alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2008]","start":120950749,"end":120977216,"strand":1,"description":"inhibitor of growth family member 3 [Source:HGNC Symbol;Acc:HGNC:14587]"}, {"versioned_ensembl_gene_id":"ENSG00000100121.12","gene_symbol":"GGTLC2","gene_name":"gamma-glutamyltransferase light chain 2 [Source:HGNC Symbol;Acc:HGNC:18596]","synonyms":"GGTL4","biotype":"protein_coding","ncbi_id":"91227","summary":"This gene encodes a protein related to enzymes that cleaves gamma-glutamyl peptide bonds in glutathione and other peptides. Unlike similar proteins, the encoded protein contains only the light chain portion and may not have catalytic activity. Alternative splicing results in multiple transcript variants. There are several related family members and related pseudogene for this gene situated in the same region of chromosome 22. [provided by RefSeq, Sep 2013]","start":22644475,"end":22647903,"strand":1,"description":"gamma-glutamyltransferase light chain 2 [Source:HGNC Symbol;Acc:HGNC:18596]"}, {"versioned_ensembl_gene_id":"ENSG00000197062.11","gene_symbol":"ZSCAN26","gene_name":"zinc finger and SCAN domain containing 26 [Source:HGNC Symbol;Acc:HGNC:12978]","synonyms":"ZNF187,SRE-ZBP","biotype":"protein_coding","ncbi_id":"7741","summary":null,"start":28267010,"end":28278224,"strand":1,"description":"zinc finger and SCAN domain containing 26 [Source:HGNC Symbol;Acc:HGNC:12978]"}, {"versioned_ensembl_gene_id":"ENSG00000259429.5","gene_symbol":"UBE2Q2P2","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]","synonyms":"UBE2QP2,UBE2Q2P3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100134869","summary":null,"start":82355142,"end":82420075,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37440]"}, {"versioned_ensembl_gene_id":"ENSG00000215456.6","gene_symbol":"BCRP4","gene_name":"breakpoint cluster region pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1017]","synonyms":"BCRL4,BCR4,BCR-4","biotype":"unprocessed_pseudogene","ncbi_id":"616","summary":null,"start":22630065,"end":22636153,"strand":1,"description":"breakpoint cluster region pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:1017]"}, {"versioned_ensembl_gene_id":"ENSG00000274376.4","gene_symbol":"ADAMTS7P1","gene_name":"ADAMTS7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49407]","synonyms":"ADAMTS7P2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390660","summary":null,"start":82298553,"end":82334609,"strand":1,"description":"ADAMTS7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49407]"}, {"versioned_ensembl_gene_id":"ENSG00000251427.1","gene_symbol":"AC111000.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69144734,"end":69147671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243099.1","gene_symbol":"AC020983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138688980,"end":138689522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213149.3","gene_symbol":"CNN2P9","gene_name":"calponin 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39534]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441166","summary":null,"start":110858239,"end":110859147,"strand":1,"description":"calponin 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39534]"}, {"versioned_ensembl_gene_id":"ENSG00000198642.6","gene_symbol":"KLHL9","gene_name":"kelch like family member 9 [Source:HGNC Symbol;Acc:HGNC:18732]","synonyms":"KIAA1354,FLJ13568","biotype":"protein_coding","ncbi_id":"55958","summary":"This gene encodes a protein that belongs to the kelch repeat-containing family, and contains an N-terminal BTB/POZ domain, a BACK domain and six C-terminal kelch repeats. The encoded protein is a component of a complex with cullin 3-based E3 ligase, which plays a role in mitosis. This protein complex is a cell cycle regulator, and functions in the organization and integrity of the spindle midzone in anaphase and the completion of cytokinesis. The complex is required for the removal of the chromosomal passenger protein aurora B from mitotic chromosomes. [provided by RefSeq, Jul 2016]","start":21329671,"end":21335380,"strand":-1,"description":"kelch like family member 9 [Source:HGNC Symbol;Acc:HGNC:18732]"}, {"versioned_ensembl_gene_id":"ENSG00000254741.1","gene_symbol":"AC067930.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143579636,"end":143580670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187778.13","gene_symbol":"MCRS1","gene_name":"microspherule protein 1 [Source:HGNC Symbol;Acc:HGNC:6960]","synonyms":"P78,MSP58,MCRS2,INO80Q,ICP22BP","biotype":"protein_coding","ncbi_id":"10445","summary":null,"start":49556544,"end":49568153,"strand":-1,"description":"microspherule protein 1 [Source:HGNC Symbol;Acc:HGNC:6960]"}, {"versioned_ensembl_gene_id":"ENSG00000257097.1","gene_symbol":"CLIP1-AS1","gene_name":"CLIP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48586]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507066","summary":null,"start":122395542,"end":122400857,"strand":1,"description":"CLIP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48586]"}, {"versioned_ensembl_gene_id":"ENSG00000253770.1","gene_symbol":"HMGB1P23","gene_name":"high mobility group box 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39114]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873891","summary":null,"start":29218905,"end":29219472,"strand":1,"description":"high mobility group box 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:39114]"}, {"versioned_ensembl_gene_id":"ENSG00000179913.10","gene_symbol":"B3GNT3","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:13528]","synonyms":"TMEM3,HP10328,beta3Gn-T3,B3GNT-3,B3GN-T3","biotype":"protein_coding","ncbi_id":"10331","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II transmembrane protein and contains a signal anchor that is not cleaved. It prefers the substrates of lacto-N-tetraose and lacto-N-neotetraose, and is involved in the biosynthesis of poly-N-acetyllactosamine chains and the biosynthesis of the backbone structure of dimeric sialyl Lewis a. It plays dominant roles in L-selectin ligand biosynthesis, lymphocyte homing and lymphocyte trafficking. [provided by RefSeq, Jul 2008]","start":17794828,"end":17813082,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:13528]"}, {"versioned_ensembl_gene_id":"ENSG00000226597.1","gene_symbol":"IFNWP9","gene_name":"interferon omega 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:5455]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130671","summary":null,"start":21190654,"end":21191244,"strand":-1,"description":"interferon omega 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:5455]"}, {"versioned_ensembl_gene_id":"ENSG00000279070.2","gene_symbol":"AC073263.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74196698,"end":74198560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131143.8","gene_symbol":"COX4I1","gene_name":"cytochrome c oxidase subunit 4I1 [Source:HGNC Symbol;Acc:HGNC:2265]","synonyms":"COX4-1,COX4","biotype":"protein_coding","ncbi_id":"1327","summary":"Cytochrome c oxidase (COX) is the terminal enzyme of the mitochondrial respiratory chain. It is a multi-subunit enzyme complex that couples the transfer of electrons from cytochrome c to molecular oxygen and contributes to a proton electrochemical gradient across the inner mitochondrial membrane. The complex consists of 13 mitochondrial- and nuclear-encoded subunits. The mitochondrially-encoded subunits perform the electron transfer and proton pumping activities. The functions of the nuclear-encoded subunits are unknown but they may play a role in the regulation and assembly of the complex. This gene encodes the nuclear-encoded subunit IV isoform 1 of the human mitochondrial respiratory chain enzyme. It is located at the 3' of the NOC4 (neighbor of COX4) gene in a head-to-head orientation, and shares a promoter with it. Pseudogenes related to this gene are located on chromosomes 13 and 14. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":85798633,"end":85807044,"strand":1,"description":"cytochrome c oxidase subunit 4I1 [Source:HGNC Symbol;Acc:HGNC:2265]"}, {"versioned_ensembl_gene_id":"ENSG00000100416.12","gene_symbol":"TRMU","gene_name":"tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase [Source:HGNC Symbol;Acc:HGNC:25481]","synonyms":"TRMT,MTO2,FLJ10140","biotype":"protein_coding","ncbi_id":"55687","summary":"This nuclear gene encodes a mitochondrial tRNA-modifying enzyme. The encoded protein catalyzes the 2-thiolation of uridine on the wobble positions of tRNA(Lys), tRNA(Glu), and tRNA(Gln), resulting in the formation of 5-taurinomethyl-2-thiouridine moieties. Mutations in this gene may cause transient infantile liver failure. Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":46330875,"end":46357340,"strand":1,"description":"tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase [Source:HGNC Symbol;Acc:HGNC:25481]"}, {"versioned_ensembl_gene_id":"ENSG00000220748.2","gene_symbol":"AL032822.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23971879,"end":23972941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141504.11","gene_symbol":"SAT2","gene_name":"spermidine/spermine N1-acetyltransferase family member 2 [Source:HGNC Symbol;Acc:HGNC:23160]","synonyms":"SSAT2","biotype":"protein_coding","ncbi_id":"112483","summary":null,"start":7626234,"end":7627876,"strand":-1,"description":"spermidine/spermine N1-acetyltransferase family member 2 [Source:HGNC Symbol;Acc:HGNC:23160]"}, {"versioned_ensembl_gene_id":"ENSG00000251633.3","gene_symbol":"GYG1P1","gene_name":"glycogenin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39712]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132965","summary":null,"start":73905357,"end":73915010,"strand":-1,"description":"glycogenin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39712]"}, {"versioned_ensembl_gene_id":"ENSG00000197746.13","gene_symbol":"PSAP","gene_name":"prosaposin [Source:HGNC Symbol;Acc:HGNC:9498]","synonyms":"SAP1,GLBA","biotype":"protein_coding","ncbi_id":"5660","summary":"This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":71816298,"end":71851375,"strand":-1,"description":"prosaposin [Source:HGNC Symbol;Acc:HGNC:9498]"}, {"versioned_ensembl_gene_id":"ENSG00000144647.5","gene_symbol":"POMGNT2","gene_name":"protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) [Source:HGNC Symbol;Acc:HGNC:25902]","synonyms":"GTDC2,FLJ14566,C3orf39,AGO61","biotype":"protein_coding","ncbi_id":"84892","summary":"This gene encodes a protein with glycosyltransferase activity although its function is not currently known. [provided by RefSeq, Sep 2012]","start":43079232,"end":43106076,"strand":-1,"description":"protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) [Source:HGNC Symbol;Acc:HGNC:25902]"}, {"versioned_ensembl_gene_id":"ENSG00000253667.2","gene_symbol":"AC100821.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53971231,"end":53974210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163704.11","gene_symbol":"PRRT3","gene_name":"proline rich transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:26591]","synonyms":"FLJ33674","biotype":"protein_coding","ncbi_id":"285368","summary":null,"start":9945542,"end":9952394,"strand":-1,"description":"proline rich transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:26591]"}, {"versioned_ensembl_gene_id":"ENSG00000278856.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816482,"end":54830789,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000132821.11","gene_symbol":"VSTM2L","gene_name":"V-set and transmembrane domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:16096]","synonyms":"dJ1118M15.2,C20orf102","biotype":"protein_coding","ncbi_id":"128434","summary":null,"start":37903104,"end":37945350,"strand":1,"description":"V-set and transmembrane domain containing 2 like [Source:HGNC Symbol;Acc:HGNC:16096]"}, {"versioned_ensembl_gene_id":"ENSG00000225027.2","gene_symbol":"IFNWP4","gene_name":"interferon omega 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:5453]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21106543,"end":21106836,"strand":1,"description":"interferon omega 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:5453]"}, {"versioned_ensembl_gene_id":"ENSG00000128908.15","gene_symbol":"INO80","gene_name":"INO80 complex subunit [Source:HGNC Symbol;Acc:HGNC:26956]","synonyms":"KIAA1259,INOC1,INO80A,Ino80,hINO80","biotype":"protein_coding","ncbi_id":"54617","summary":"This gene encodes a subunit of the chromatin remodeling complex, which is classified into subfamilies depending on sequence features apart from the conserved ATPase domain. This protein is the catalytic ATPase subunit of the INO80 chromatin remodeling complex, which is characterized by a DNA-binding domain. This protein is proposed to bind DNA and be recruited by the YY1 transcription factor to activate certain genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":40978880,"end":41116354,"strand":-1,"description":"INO80 complex subunit [Source:HGNC Symbol;Acc:HGNC:26956]"}, {"versioned_ensembl_gene_id":"ENSG00000057704.12","gene_symbol":"TMCC3","gene_name":"transmembrane and coiled-coil domain family 3 [Source:HGNC Symbol;Acc:HGNC:29199]","synonyms":"KIAA1145","biotype":"protein_coding","ncbi_id":"57458","summary":null,"start":94567124,"end":94650562,"strand":-1,"description":"transmembrane and coiled-coil domain family 3 [Source:HGNC Symbol;Acc:HGNC:29199]"}, {"versioned_ensembl_gene_id":"ENSG00000168824.14","gene_symbol":"HGNC:18790","gene_name":"Neuron-specific protein family member 1 [Source:UniProtKB/Swiss-Prot;Acc:P42857]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4348140,"end":4419058,"strand":1,"description":"Neuron-specific protein family member 1 [Source:UniProtKB/Swiss-Prot;Acc:P42857]"}, {"versioned_ensembl_gene_id":"ENSG00000257847.1","gene_symbol":"LSM3P2","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44347]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100303745","summary":null,"start":94590821,"end":94591093,"strand":1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44347]"}, {"versioned_ensembl_gene_id":"ENSG00000259617.1","gene_symbol":"AC020661.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40999274,"end":41004865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273870.1","gene_symbol":"AL138721.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35070871,"end":35071049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143379.12","gene_symbol":"SETDB1","gene_name":"SET domain bifurcated 1 [Source:HGNC Symbol;Acc:HGNC:10761]","synonyms":"KIAA0067,KG1T,ESET,TDRD21,KMT1E","biotype":"protein_coding","ncbi_id":"9869","summary":"This gene encodes a histone methyltransferase which regulates histone methylation, gene silencing, and transcriptional repression. This gene has been identified as a target for treatment in Huntington Disease, given that gene silencing and transcription dysfunction likely play a role in the disease pathogenesis. Alternatively spliced transcript variants of this gene have been described.[provided by RefSeq, Jun 2011]","start":150926263,"end":150964744,"strand":1,"description":"SET domain bifurcated 1 [Source:HGNC Symbol;Acc:HGNC:10761]"}, {"versioned_ensembl_gene_id":"ENSG00000234589.4","gene_symbol":"AC125807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3071532,"end":3072145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276357.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850475,"end":54867233,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000250899.3","gene_symbol":"AC125807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3041437,"end":3044950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263393.1","gene_symbol":"AC011825.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32122400,"end":32124478,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228550.1","gene_symbol":"AC073583.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7113005,"end":7113404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228677.1","gene_symbol":"TTC3-AS1","gene_name":"TTC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40595]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874006","summary":null,"start":37187666,"end":37193926,"strand":-1,"description":"TTC3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40595]"}, {"versioned_ensembl_gene_id":"ENSG00000270116.1","gene_symbol":"AP001429.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37100814,"end":37101343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226960.1","gene_symbol":"MTCO1P21","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52086]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075164","summary":null,"start":93927714,"end":93928302,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52086]"}, {"versioned_ensembl_gene_id":"ENSG00000276512.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:NCBI gene;Acc:79166]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79166","summary":null,"start":54707913,"end":54713335,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:NCBI gene;Acc:79166]"}, {"versioned_ensembl_gene_id":"ENSG00000272620.1","gene_symbol":"AFAP1-AS1","gene_name":"AFAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28141]","synonyms":"MGC10981,AFAP1AS,AFAP1-AS","biotype":"antisense_RNA","ncbi_id":"84740","summary":"This gene produces a long non-coding RNA that is overexpressed in tumor cells and may promote cancer cell metastasis. [provided by RefSeq, Dec 2017]","start":7754090,"end":7778928,"strand":1,"description":"AFAP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28141]"}, {"versioned_ensembl_gene_id":"ENSG00000236689.1","gene_symbol":"MTCO2P21","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52150]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075191","summary":null,"start":93926615,"end":93927569,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52150]"}, {"versioned_ensembl_gene_id":"ENSG00000084453.16","gene_symbol":"SLCO1A2","gene_name":"solute carrier organic anion transporter family member 1A2 [Source:HGNC Symbol;Acc:HGNC:10956]","synonyms":"OATP,SLC21A3,OATP1A2,OATP-A","biotype":"protein_coding","ncbi_id":"6579","summary":"This gene encodes a sodium-independent transporter which mediates cellular uptake of organic ions in the liver. Its substrates include bile acids, bromosulphophthalein, and some steroidal compounds. The protein is a member of the SLC21A family of solute carriers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":21264600,"end":21419594,"strand":-1,"description":"solute carrier organic anion transporter family member 1A2 [Source:HGNC Symbol;Acc:HGNC:10956]"}, {"versioned_ensembl_gene_id":"ENSG00000251416.1","gene_symbol":"AC103879.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177686673,"end":177691068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237196.1","gene_symbol":"HCG24","gene_name":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]","synonyms":"dJ1033B10.15","biotype":"processed_transcript","ncbi_id":"414768","summary":null,"start":33066394,"end":33069387,"strand":1,"description":"HLA complex group 24 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:23500]"}, {"versioned_ensembl_gene_id":"ENSG00000228386.2","gene_symbol":"AL031668.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34014969,"end":34017749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164938.13","gene_symbol":"TP53INP1","gene_name":"tumor protein p53 inducible nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:18022]","synonyms":"FLJ22139,DKFZp434M1317,TP53INP1B,TP53INP1A,Teap,SIP,P53DINP1","biotype":"protein_coding","ncbi_id":"94241","summary":null,"start":94925972,"end":94949411,"strand":-1,"description":"tumor protein p53 inducible nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:18022]"}, {"versioned_ensembl_gene_id":"ENSG00000276073.1","gene_symbol":"AL034549.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33985617,"end":33988989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261606.5","gene_symbol":"AC091230.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":74816223,"end":74831795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220666.2","gene_symbol":"RCC2P7","gene_name":"regulator of chromosome condensation 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42383]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442221","summary":null,"start":56431950,"end":56433213,"strand":-1,"description":"regulator of chromosome condensation 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42383]"}, {"versioned_ensembl_gene_id":"ENSG00000243708.10","gene_symbol":"PLA2G4B","gene_name":"phospholipase A2 group IVB [Source:HGNC Symbol;Acc:HGNC:9036]","synonyms":"HsT16992,cPLA2-beta","biotype":"protein_coding","ncbi_id":"100137049","summary":"This gene encodes a member of the cytosolic phospholipase A2 protein family. Phospholipase A2 enzymes hydrolyze the sn-2 bond of phospholipids, releasing lysophospholipids and fatty acids. This enzyme may be associated with mitochondria and early endosomes. Most tissues also express read-through transcripts from the upstream gene into this gene, some of which may encode fusion proteins combining the N-terminus of the upstream gene including its JmjC domain with the almost complete coding region of this gene, including the C2 and cytoplasmic phospholipase A2 domains. [provided by RefSeq, Jul 2008]","start":41837775,"end":41848147,"strand":1,"description":"phospholipase A2 group IVB [Source:HGNC Symbol;Acc:HGNC:9036]"}, {"versioned_ensembl_gene_id":"ENSG00000176912.3","gene_symbol":"TYMSOS","gene_name":"TYMS opposite strand [Source:HGNC Symbol;Acc:HGNC:29553]","synonyms":"C18orf56","biotype":"bidirectional_promoter_lncRNA","ncbi_id":"494514","summary":null,"start":641320,"end":658340,"strand":-1,"description":"TYMS opposite strand [Source:HGNC Symbol;Acc:HGNC:29553]"}, {"versioned_ensembl_gene_id":"ENSG00000280380.1","gene_symbol":"AC009831.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31982899,"end":31986087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249668.1","gene_symbol":"KRT18P56","gene_name":"keratin 18 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:43923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479027","summary":null,"start":40066651,"end":40067200,"strand":1,"description":"keratin 18 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:43923]"}, {"versioned_ensembl_gene_id":"ENSG00000204822.6","gene_symbol":"MRPL53","gene_name":"mitochondrial ribosomal protein L53 [Source:HGNC Symbol;Acc:HGNC:16684]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116540","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. A pseudogene corresponding to this gene is found on chromosome 1p. [provided by RefSeq, Jul 2008]","start":74471958,"end":74473322,"strand":-1,"description":"mitochondrial ribosomal protein L53 [Source:HGNC Symbol;Acc:HGNC:16684]"}, {"versioned_ensembl_gene_id":"ENSG00000265273.1","gene_symbol":"AC009831.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31962178,"end":31963618,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250048.2","gene_symbol":"LINC00603","gene_name":"long intergenic non-protein coding RNA 603 [Source:HGNC Symbol;Acc:HGNC:43918]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467077","summary":null,"start":39892138,"end":40053324,"strand":1,"description":"long intergenic non-protein coding RNA 603 [Source:HGNC Symbol;Acc:HGNC:43918]"}, {"versioned_ensembl_gene_id":"ENSG00000248651.1","gene_symbol":"GCSHP1","gene_name":"glycine cleavage system protein H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480441","summary":null,"start":39888576,"end":39889059,"strand":-1,"description":"glycine cleavage system protein H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43922]"}, {"versioned_ensembl_gene_id":"ENSG00000233033.1","gene_symbol":"CASK-AS1","gene_name":"CASK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40126]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873928","summary":null,"start":41520036,"end":41522336,"strand":1,"description":"CASK antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40126]"}, {"versioned_ensembl_gene_id":"ENSG00000218512.2","gene_symbol":"SPTLC1P2","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39669]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874498","summary":null,"start":23856698,"end":23856818,"strand":-1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39669]"}, {"versioned_ensembl_gene_id":"ENSG00000261084.1","gene_symbol":"AC116553.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35912120,"end":35912516,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188921.13","gene_symbol":"HACD4","gene_name":"3-hydroxyacyl-CoA dehydratase 4 [Source:HGNC Symbol;Acc:HGNC:20920]","synonyms":"PTPLAD2,OTTHUMG00000021016,Em:AL662879.1","biotype":"protein_coding","ncbi_id":"401494","summary":null,"start":20999515,"end":21031636,"strand":-1,"description":"3-hydroxyacyl-CoA dehydratase 4 [Source:HGNC Symbol;Acc:HGNC:20920]"}, {"versioned_ensembl_gene_id":"ENSG00000279666.1","gene_symbol":"AC116553.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35903117,"end":35904916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229251.3","gene_symbol":"HNRNPA1P8","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39126]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402562","summary":null,"start":84983556,"end":84984506,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39126]"}, {"versioned_ensembl_gene_id":"ENSG00000136206.3","gene_symbol":"SPDYE1","gene_name":"speedy/RINGO cell cycle regulator family member E1 [Source:HGNC Symbol;Acc:HGNC:16408]","synonyms":"SPDYE,Ringo1,WBSCR19","biotype":"protein_coding","ncbi_id":"285955","summary":"This gene is located at chromosome 7p13 which is close to the Williams Beuren syndrome chromosome region 7q11.23. [provided by RefSeq, Jul 2008]","start":44000889,"end":44010122,"strand":1,"description":"speedy/RINGO cell cycle regulator family member E1 [Source:HGNC Symbol;Acc:HGNC:16408]"}, {"versioned_ensembl_gene_id":"ENSG00000132463.13","gene_symbol":"GRSF1","gene_name":"G-rich RNA sequence binding factor 1 [Source:HGNC Symbol;Acc:HGNC:4610]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2926","summary":"The protein encoded by this gene is a cellular protein that binds RNAs containing the G-rich element. The protein is localized in the cytoplasm, and has been shown to stimulate translation of viral mRNAs in vitro. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":70815782,"end":70839945,"strand":-1,"description":"G-rich RNA sequence binding factor 1 [Source:HGNC Symbol;Acc:HGNC:4610]"}, {"versioned_ensembl_gene_id":"ENSG00000235139.2","gene_symbol":"AC003984.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84532476,"end":84584322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164172.18","gene_symbol":"MOCS2","gene_name":"molybdenum cofactor synthesis 2 [Source:HGNC Symbol;Acc:HGNC:7193]","synonyms":"MOCO1","biotype":"protein_coding","ncbi_id":"4338","summary":"Eukaryotic molybdoenzymes use a unique molybdenum cofactor (MoCo) consisting of a pterin, termed molybdopterin, and the catalytically active metal molybdenum. MoCo is synthesized from precursor Z by the heterodimeric enzyme molybdopterin synthase. The large and small subunits of molybdopterin synthase are both encoded from this gene by overlapping open reading frames. The proteins were initially thought to be encoded from a bicistronic transcript. They are now thought to be encoded from monocistronic transcripts. Alternatively spliced transcripts have been found for this locus that encode the large and small subunits. [provided by RefSeq, Jul 2008]","start":53095679,"end":53110063,"strand":-1,"description":"molybdenum cofactor synthesis 2 [Source:HGNC Symbol;Acc:HGNC:7193]"}, {"versioned_ensembl_gene_id":"ENSG00000281767.1","gene_symbol":"AC093627.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165082,"end":168277,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170162.13","gene_symbol":"VGLL2","gene_name":"vestigial like family member 2 [Source:HGNC Symbol;Acc:HGNC:20232]","synonyms":null,"biotype":"protein_coding","ncbi_id":"245806","summary":"This gene encodes a protein with a transcriptional enhancer factor 1 (TEF-1) interaction domain. The encoded protein may act as a co-factor of TEF-1 regulated gene expression during skeletal muscle development. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012]","start":117265558,"end":117273565,"strand":1,"description":"vestigial like family member 2 [Source:HGNC Symbol;Acc:HGNC:20232]"}, {"versioned_ensembl_gene_id":"ENSG00000171953.15","gene_symbol":"ATPAF2","gene_name":"ATP synthase mitochondrial F1 complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:18802]","synonyms":"MGC29736,LP3663,Atp12p,ATP12","biotype":"protein_coding","ncbi_id":"91647","summary":"This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":17977409,"end":18039209,"strand":-1,"description":"ATP synthase mitochondrial F1 complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:18802]"}, {"versioned_ensembl_gene_id":"ENSG00000204019.4","gene_symbol":"CT83","gene_name":"cancer/testis antigen 83 [Source:HGNC Symbol;Acc:HGNC:33494]","synonyms":"KK-LC-1,FLJ22913,FLJ20611,CXorf61","biotype":"protein_coding","ncbi_id":"203413","summary":null,"start":116461682,"end":116463003,"strand":-1,"description":"cancer/testis antigen 83 [Source:HGNC Symbol;Acc:HGNC:33494]"}, {"versioned_ensembl_gene_id":"ENSG00000128965.11","gene_symbol":"CHAC1","gene_name":"ChaC glutathione specific gamma-glutamylcyclotransferase 1 [Source:HGNC Symbol;Acc:HGNC:28680]","synonyms":"MGC4504","biotype":"protein_coding","ncbi_id":"79094","summary":"This gene encodes a member of the gamma-glutamylcyclotransferase family of proteins. The encoded protein has been shown to promote neuronal differentiation by deglycination of the Notch receptor, which prevents receptor maturation and inhibits Notch signaling. This protein may also play a role in the unfolded protein response, and in regulation of glutathione levels and oxidative balance in the cell. Elevated expression of this gene may indicate increased risk of cancer recurrence among breast and ovarian cancer patients. [provided by RefSeq, Sep 2016]","start":40952962,"end":40956519,"strand":1,"description":"ChaC glutathione specific gamma-glutamylcyclotransferase 1 [Source:HGNC Symbol;Acc:HGNC:28680]"}, {"versioned_ensembl_gene_id":"ENSG00000273884.4","gene_symbol":"LILRA3","gene_name":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]","synonyms":"HM43,HM31,LIR4,CD85e,LIR-4,ILT6","biotype":"protein_coding","ncbi_id":"11026","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]","start":54294043,"end":54306352,"strand":-1,"description":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]"}, {"versioned_ensembl_gene_id":"ENSG00000237884.1","gene_symbol":"AL845454.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29995625,"end":29996621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258631.2","gene_symbol":"AC110023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93589867,"end":93760799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261558.1","gene_symbol":"LINC01859","gene_name":"long intergenic non-protein coding RNA 1859 [Source:HGNC Symbol;Acc:HGNC:52677]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929164","summary":null,"start":23015075,"end":23023697,"strand":-1,"description":"long intergenic non-protein coding RNA 1859 [Source:HGNC Symbol;Acc:HGNC:52677]"}, {"versioned_ensembl_gene_id":"ENSG00000172352.5","gene_symbol":"CDY1B","gene_name":"chromodomain Y-linked 1B [Source:HGNC Symbol;Acc:HGNC:23920]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253175","summary":"This gene encodes a protein containing a chromodomain and a histone acetyltransferase catalytic domain. Chromodomain proteins are components of heterochromatin-like complexes and can act as gene repressors. This protein is localized to the nucleus of late spermatids where histone hyperacetylation takes place. Histone hyperacetylation is thought to facilitate the transition in which protamines replace histones as the major DNA-packaging protein. The human chromosome Y has two identical copies of this gene within a palindromic region; this record represents the more centromeric copy. Chromosome Y also contains a pair of closely related genes in another more telomeric palindrome as well as several related pseudogenes. Two protein isoforms are encoded by transcript variants of this gene. Additional transcript variants have been described, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":24045229,"end":24048019,"strand":-1,"description":"chromodomain Y-linked 1B [Source:HGNC Symbol;Acc:HGNC:23920]"}, {"versioned_ensembl_gene_id":"ENSG00000235814.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"antisense_RNA","ncbi_id":"80862","summary":null,"start":29990513,"end":30051230,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000236434.2","gene_symbol":"AL162430.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51264916,"end":51266074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274650.1","gene_symbol":"OR6D1P","gene_name":"olfactory receptor family 6 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14849]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"220974","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":45258185,"end":45259123,"strand":1,"description":"olfactory receptor family 6 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14849]"}, {"versioned_ensembl_gene_id":"ENSG00000279809.1","gene_symbol":"AC005538.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":233865496,"end":233867359,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277286.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54686316,"end":54698662,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000228465.1","gene_symbol":"TRAPPC2P10","gene_name":"trafficking protein particle complex 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37732]","synonyms":"TRAPPC2P5B","biotype":"unprocessed_pseudogene","ncbi_id":"414752","summary":null,"start":23967564,"end":23970694,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:37732]"}, {"versioned_ensembl_gene_id":"ENSG00000224618.1","gene_symbol":"AC096921.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30626423,"end":30626797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224103.7","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":32986539,"end":33002744,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000228579.1","gene_symbol":"AL662824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33001420,"end":33001829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228532.4","gene_symbol":"AC005000.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115718942,"end":115719229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226968.1","gene_symbol":"LINC00423","gene_name":"long intergenic non-protein coding RNA 423 [Source:HGNC Symbol;Acc:HGNC:42758]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874167","summary":null,"start":32877431,"end":32911650,"strand":-1,"description":"long intergenic non-protein coding RNA 423 [Source:HGNC Symbol;Acc:HGNC:42758]"}, {"versioned_ensembl_gene_id":"ENSG00000135677.10","gene_symbol":"GNS","gene_name":"glucosamine (N-acetyl)-6-sulfatase [Source:HGNC Symbol;Acc:HGNC:4422]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2799","summary":"The product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome. [provided by RefSeq, Jul 2008]","start":64713445,"end":64759447,"strand":-1,"description":"glucosamine (N-acetyl)-6-sulfatase [Source:HGNC Symbol;Acc:HGNC:4422]"}, {"versioned_ensembl_gene_id":"ENSG00000223922.1","gene_symbol":"ASS1P2","gene_name":"argininosuccinate synthetase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:765]","synonyms":"ASSP2","biotype":"processed_pseudogene","ncbi_id":"447","summary":null,"start":38810432,"end":38811654,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:765]"}, {"versioned_ensembl_gene_id":"ENSG00000227960.1","gene_symbol":"AL138799.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":81505099,"end":81506296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274163.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786260,"end":54790260,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000186523.14","gene_symbol":"FAM86B1","gene_name":"family with sequence similarity 86 member B1 [Source:HGNC Symbol;Acc:HGNC:28268]","synonyms":"MGC16279","biotype":"protein_coding","ncbi_id":"85002","summary":null,"start":12182096,"end":12194133,"strand":-1,"description":"family with sequence similarity 86 member B1 [Source:HGNC Symbol;Acc:HGNC:28268]"}, {"versioned_ensembl_gene_id":"ENSG00000213188.3","gene_symbol":"YBX1P4","gene_name":"Y-box binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42425]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131012","summary":null,"start":152128879,"end":152129686,"strand":1,"description":"Y-box binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42425]"}, {"versioned_ensembl_gene_id":"ENSG00000257356.2","gene_symbol":"BNIP3P6","gene_name":"BCL2 interacting protein 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39659]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129777","summary":null,"start":18418775,"end":18419273,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39659]"}, {"versioned_ensembl_gene_id":"ENSG00000257171.2","gene_symbol":"CR383658.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18395626,"end":18412264,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171861.10","gene_symbol":"MRM3","gene_name":"mitochondrial rRNA methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:18485]","synonyms":"RNMTL1,RMTL1,HC90,FLJ10581","biotype":"protein_coding","ncbi_id":"55178","summary":"Efficient translation of mitochondrial-derived transcripts requires proper assembly of the large subunit of the mitochondrial ribosome. Central to the biogenesis of this large subunit is the A-loop of mitochondrial 16S rRNA, which is modified by three rRNA methyltransferases located near mtDNA nucleoids. The protein encoded by this gene methylates G(1370) of 16S rRNA, and this modification is necessary for proper ribosomal large subnit assembly. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":782273,"end":792509,"strand":1,"description":"mitochondrial rRNA methyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:18485]"}, {"versioned_ensembl_gene_id":"ENSG00000132972.18","gene_symbol":"RNF17","gene_name":"ring finger protein 17 [Source:HGNC Symbol;Acc:HGNC:10060]","synonyms":"TDRD4,SPATA23,Mmip-2,FLJ11045","biotype":"protein_coding","ncbi_id":"56163","summary":"This gene is similar to a mouse gene that encodes a testis-specific protein containing a RING finger domain. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, May 2010]","start":24764152,"end":24879921,"strand":1,"description":"ring finger protein 17 [Source:HGNC Symbol;Acc:HGNC:10060]"}, {"versioned_ensembl_gene_id":"ENSG00000226662.2","gene_symbol":"CHMP1AP1","gene_name":"charged multivesicular body protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39514]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646597","summary":null,"start":27686810,"end":27687471,"strand":-1,"description":"charged multivesicular body protein 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39514]"}, {"versioned_ensembl_gene_id":"ENSG00000278603.1","gene_symbol":"AC245033.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":82472203,"end":82472426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275632.1","gene_symbol":"AL035461.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6000418,"end":6000941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248995.2","gene_symbol":"LINC02231","gene_name":"long intergenic non-protein coding RNA 2231 [Source:HGNC Symbol;Acc:HGNC:53100]","synonyms":"RP11-766N7.4","biotype":"lincRNA","ncbi_id":"109729131","summary":null,"start":64920845,"end":64982524,"strand":-1,"description":"long intergenic non-protein coding RNA 2231 [Source:HGNC Symbol;Acc:HGNC:53100]"}, {"versioned_ensembl_gene_id":"ENSG00000173542.8","gene_symbol":"MOB1B","gene_name":"MOB kinase activator 1B [Source:HGNC Symbol;Acc:HGNC:29801]","synonyms":"MOBKL1A,MOB4A","biotype":"protein_coding","ncbi_id":"92597","summary":"The protein encoded by this gene is similar to the yeast Mob1 protein. Yeast Mob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":70902326,"end":71022449,"strand":1,"description":"MOB kinase activator 1B [Source:HGNC Symbol;Acc:HGNC:29801]"}, {"versioned_ensembl_gene_id":"ENSG00000267208.1","gene_symbol":"AC209539.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41238001,"end":41238465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075275.16","gene_symbol":"CELSR1","gene_name":"cadherin EGF LAG seven-pass G-type receptor 1 [Source:HGNC Symbol;Acc:HGNC:1850]","synonyms":"ME2,HFMI2,FMI2,CDHF9,ADGRC1","biotype":"protein_coding","ncbi_id":"9620","summary":"The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. This particular member is a developmentally regulated, neural-specific gene which plays an unspecified role in early embryogenesis. [provided by RefSeq, Jul 2008]","start":46360834,"end":46537170,"strand":-1,"description":"cadherin EGF LAG seven-pass G-type receptor 1 [Source:HGNC Symbol;Acc:HGNC:1850]"}, {"versioned_ensembl_gene_id":"ENSG00000096264.13","gene_symbol":"NCR2","gene_name":"natural cytotoxicity triggering receptor 2 [Source:HGNC Symbol;Acc:HGNC:6732]","synonyms":"NK-p44,LY95,CD336","biotype":"protein_coding","ncbi_id":"9436","summary":null,"start":41335655,"end":41350887,"strand":1,"description":"natural cytotoxicity triggering receptor 2 [Source:HGNC Symbol;Acc:HGNC:6732]"}, {"versioned_ensembl_gene_id":"ENSG00000278292.1","gene_symbol":"RFPL4AP6","gene_name":"ret finger protein like 4A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45142]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130079","summary":null,"start":29432944,"end":29435005,"strand":1,"description":"ret finger protein like 4A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45142]"}, {"versioned_ensembl_gene_id":"ENSG00000275928.2","gene_symbol":"REXO1L11P","gene_name":"REXO1 like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:44434]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288470","summary":null,"start":85733419,"end":85737278,"strand":1,"description":"REXO1 like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:44434]"}, {"versioned_ensembl_gene_id":"ENSG00000238103.4","gene_symbol":"RPL9P7","gene_name":"ribosomal protein L9 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:30335]","synonyms":"RPL9L1,RPL9P1","biotype":"processed_pseudogene","ncbi_id":"6126","summary":null,"start":23836742,"end":23837321,"strand":-1,"description":"ribosomal protein L9 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:30335]"}, {"versioned_ensembl_gene_id":"ENSG00000142606.15","gene_symbol":"MMEL1","gene_name":"membrane metalloendopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:14668]","synonyms":"SEP,NL2,NL1,NEPII,MMEL2","biotype":"protein_coding","ncbi_id":"79258","summary":"The protein encoded by this gene is a member of the neutral endopeptidase (NEP) or membrane metallo-endopeptidase (MME) family. Family members play important roles in pain perception, arterial pressure regulation, phosphate metabolism and homeostasis. This protein is a type II transmembrane protein and is thought to be expressed as a secreted protein. This gene is expressed mainly in testis with weak expression in the brain, kidney, and heart. [provided by RefSeq, Jul 2008]","start":2590639,"end":2632990,"strand":-1,"description":"membrane metalloendopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:14668]"}, {"versioned_ensembl_gene_id":"ENSG00000260492.2","gene_symbol":"CISTR","gene_name":"chondrogenesis-associated transcript [Source:HGNC Symbol;Acc:HGNC:49426]","synonyms":"re52431,CISTRACT,CISTR-ACT","biotype":"lincRNA","ncbi_id":"102216268","summary":null,"start":53750447,"end":53757034,"strand":-1,"description":"chondrogenesis-associated transcript [Source:HGNC Symbol;Acc:HGNC:49426]"}, {"versioned_ensembl_gene_id":"ENSG00000243175.1","gene_symbol":"RPSAP36","gene_name":"ribosomal protein SA pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35727]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100128888","summary":null,"start":143424753,"end":143426013,"strand":1,"description":"ribosomal protein SA pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35727]"}, {"versioned_ensembl_gene_id":"ENSG00000230555.2","gene_symbol":"AL450326.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43420738,"end":43422100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253152.1","gene_symbol":"IGLV3-17","gene_name":"immunoglobulin lambda variable 3-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5902]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28798","summary":null,"start":22738944,"end":22739187,"strand":1,"description":"immunoglobulin lambda variable 3-17 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5902]"}, {"versioned_ensembl_gene_id":"ENSG00000260733.1","gene_symbol":"AC046158.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78495926,"end":78506568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270058.1","gene_symbol":"AC040170.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86221423,"end":86222729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253546.1","gene_symbol":"IGLVVI-22-1","gene_name":"immunoglobulin lambda variable (VI)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15689]","synonyms":"IGLV(VI)-22-1","biotype":"IG_V_pseudogene","ncbi_id":"84091","summary":null,"start":22700760,"end":22700970,"strand":1,"description":"immunoglobulin lambda variable (VI)-22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15689]"}, {"versioned_ensembl_gene_id":"ENSG00000255200.1","gene_symbol":"PGAM1P8","gene_name":"phosphoglycerate mutase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42455]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"440043","summary":null,"start":65174117,"end":65176470,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42455]"}, {"versioned_ensembl_gene_id":"ENSG00000262347.2","gene_symbol":"KRTAP1-3","gene_name":"keratin associated protein 1-3 [Source:HGNC Symbol;Acc:HGNC:16771]","synonyms":"KAP1.3","biotype":"protein_coding","ncbi_id":"81850","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41034011,"end":41034982,"strand":-1,"description":"keratin associated protein 1-3 [Source:HGNC Symbol;Acc:HGNC:16771]"}, {"versioned_ensembl_gene_id":"ENSG00000277493.1","gene_symbol":"AC139769.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23842549,"end":23843230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118564.14","gene_symbol":"FBXL5","gene_name":"F-box and leucine rich repeat protein 5 [Source:HGNC Symbol;Acc:HGNC:13602]","synonyms":"FLR1,FBL5,FBL4","biotype":"protein_coding","ncbi_id":"26234","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2010]","start":15604539,"end":15681679,"strand":-1,"description":"F-box and leucine rich repeat protein 5 [Source:HGNC Symbol;Acc:HGNC:13602]"}, {"versioned_ensembl_gene_id":"ENSG00000269662.1","gene_symbol":"BNIP3P39","gene_name":"BCL2 interacting protein 3 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:49719]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421701","summary":null,"start":23798924,"end":23799477,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:49719]"}, {"versioned_ensembl_gene_id":"ENSG00000275432.1","gene_symbol":"AC022149.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14628599,"end":14628801,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260253.1","gene_symbol":"AC084262.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":29352420,"end":29353170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274386.5","gene_symbol":"TMEM269","gene_name":"transmembrane protein 269 [Source:HGNC Symbol;Acc:HGNC:52381]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100129924","summary":null,"start":42785007,"end":42816619,"strand":1,"description":"transmembrane protein 269 [Source:HGNC Symbol;Acc:HGNC:52381]"}, {"versioned_ensembl_gene_id":"ENSG00000185475.10","gene_symbol":"TMEM179B","gene_name":"transmembrane protein 179B [Source:HGNC Symbol;Acc:HGNC:33744]","synonyms":null,"biotype":"protein_coding","ncbi_id":"374395","summary":null,"start":62787415,"end":62790405,"strand":1,"description":"transmembrane protein 179B [Source:HGNC Symbol;Acc:HGNC:33744]"}, {"versioned_ensembl_gene_id":"ENSG00000177868.11","gene_symbol":"SVBP","gene_name":"small vasohibin binding protein [Source:HGNC Symbol;Acc:HGNC:29204]","synonyms":"MGC45441,CCDC23","biotype":"protein_coding","ncbi_id":"374969","summary":null,"start":42807052,"end":42817252,"strand":-1,"description":"small vasohibin binding protein [Source:HGNC Symbol;Acc:HGNC:29204]"}, {"versioned_ensembl_gene_id":"ENSG00000198915.11","gene_symbol":"RASGEF1A","gene_name":"RasGEF domain family member 1A [Source:HGNC Symbol;Acc:HGNC:24246]","synonyms":"FLJ37817,CG4853","biotype":"protein_coding","ncbi_id":"221002","summary":null,"start":43194535,"end":43266919,"strand":-1,"description":"RasGEF domain family member 1A [Source:HGNC Symbol;Acc:HGNC:24246]"}, {"versioned_ensembl_gene_id":"ENSG00000225911.1","gene_symbol":"AC009310.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":220048822,"end":220049272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148680.15","gene_symbol":"HTR7","gene_name":"5-hydroxytryptamine receptor 7 [Source:HGNC Symbol;Acc:HGNC:5302]","synonyms":"5-HT7","biotype":"protein_coding","ncbi_id":"3363","summary":"The neurotransmitter, serotonin, is thought to play a role in various cognitive and behavioral functions. The serotonin receptor encoded by this gene belongs to the superfamily of G protein-coupled receptors and the gene is a candidate locus for involvement in autistic disorder and other neuropsychiatric disorders. Three splice variants have been identified which encode proteins that differ in the length of their carboxy terminal ends. [provided by RefSeq, Jul 2008]","start":90740823,"end":90857698,"strand":-1,"description":"5-hydroxytryptamine receptor 7 [Source:HGNC Symbol;Acc:HGNC:5302]"}, {"versioned_ensembl_gene_id":"ENSG00000282026.1","gene_symbol":"DPY19L2P2","gene_name":"DPY19L2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21764]","synonyms":"FLJ36166,DKFZp434E092","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"349152","summary":null,"start":103177764,"end":103243284,"strand":-1,"description":"DPY19L2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21764]"}, {"versioned_ensembl_gene_id":"ENSG00000058404.19","gene_symbol":"CAMK2B","gene_name":"calcium/calmodulin dependent protein kinase II beta [Source:HGNC Symbol;Acc:HGNC:1461]","synonyms":"CAMKB,CAMK2,CAM2","biotype":"protein_coding","ncbi_id":"816","summary":"The product of this gene belongs to the serine/threonine protein kinase family and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells, the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a beta chain. It is possible that distinct isoforms of this chain have different cellular localizations and interact differently with calmodulin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":44217150,"end":44334577,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II beta [Source:HGNC Symbol;Acc:HGNC:1461]"}, {"versioned_ensembl_gene_id":"ENSG00000165182.10","gene_symbol":"CXorf58","gene_name":"chromosome X open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:26356]","synonyms":"FLJ25444","biotype":"protein_coding","ncbi_id":"254158","summary":null,"start":23907801,"end":23939507,"strand":1,"description":"chromosome X open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:26356]"}, {"versioned_ensembl_gene_id":"ENSG00000236373.1","gene_symbol":"AL391704.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90402521,"end":90540805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121552.3","gene_symbol":"CSTA","gene_name":"cystatin A [Source:HGNC Symbol;Acc:HGNC:2481]","synonyms":"STFA,STF1","biotype":"protein_coding","ncbi_id":"1475","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins, and kininogens. This gene encodes a stefin that functions as a cysteine protease inhibitor, forming tight complexes with papain and the cathepsins B, H, and L. The protein is one of the precursor proteins of cornified cell envelope in keratinocytes and plays a role in epidermal development and maintenance. Stefins have been proposed as prognostic and diagnostic tools for cancer. [provided by RefSeq, Jul 2008]","start":122325244,"end":122341972,"strand":1,"description":"cystatin A [Source:HGNC Symbol;Acc:HGNC:2481]"}, {"versioned_ensembl_gene_id":"ENSG00000229835.2","gene_symbol":"KHSRPP1","gene_name":"KH-type splicing regulatory protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39198]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402359","summary":null,"start":21695176,"end":21696943,"strand":1,"description":"KH-type splicing regulatory protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39198]"}, {"versioned_ensembl_gene_id":"ENSG00000184831.13","gene_symbol":"APOO","gene_name":"apolipoprotein O [Source:HGNC Symbol;Acc:HGNC:28727]","synonyms":"My025,MIC26,Mic23,MGC4825,FAM121B","biotype":"protein_coding","ncbi_id":"79135","summary":"This gene is a member of the apolipoprotein family. Members of this protein family are involved in the transport and metabolism of lipids. The encoded protein associates with HDL, LDL and VLDL lipoproteins and is characterized by chondroitin-sulfate glycosylation. This protein may be involved in preventing lipid accumulation in the myocardium in obese and diabetic patients. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 4, 5, 12 and 16.[provided by RefSeq, Sep 2009]","start":23833353,"end":23907934,"strand":-1,"description":"apolipoprotein O [Source:HGNC Symbol;Acc:HGNC:28727]"}, {"versioned_ensembl_gene_id":"ENSG00000223643.6","gene_symbol":"BX284668.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16851257,"end":16853129,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105676.13","gene_symbol":"ARMC6","gene_name":"armadillo repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:25049]","synonyms":"MGC19595","biotype":"protein_coding","ncbi_id":"93436","summary":"The function of this gene's protein product has not been determined. A related protein in mouse suggests that this protein has a conserved function. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":19033575,"end":19060311,"strand":1,"description":"armadillo repeat containing 6 [Source:HGNC Symbol;Acc:HGNC:25049]"}, {"versioned_ensembl_gene_id":"ENSG00000233860.1","gene_symbol":"AC107072.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76756960,"end":76758474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231335.1","gene_symbol":"AC121158.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":76637623,"end":76644368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224218.1","gene_symbol":"AC107072.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76758554,"end":76801964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259434.1","gene_symbol":"AC068875.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37365027,"end":37490808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282012.1","gene_symbol":"AP000357.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24691122,"end":24696003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233090.1","gene_symbol":"AC015922.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15792862,"end":15793045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250340.1","gene_symbol":"LINC02494","gene_name":"long intergenic non-protein coding RNA 2494 [Source:HGNC Symbol;Acc:HGNC:53479]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377671","summary":null,"start":58524515,"end":58536328,"strand":-1,"description":"long intergenic non-protein coding RNA 2494 [Source:HGNC Symbol;Acc:HGNC:53479]"}, {"versioned_ensembl_gene_id":"ENSG00000276855.1","gene_symbol":"AC015922.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15789016,"end":15789705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154928.16","gene_symbol":"EPHB1","gene_name":"EPH receptor B1 [Source:HGNC Symbol;Acc:HGNC:3392]","synonyms":"Hek6,EPHT2","biotype":"protein_coding","ncbi_id":"2047","summary":"Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene is a receptor for ephrin-B family members. [provided by RefSeq, Jul 2008]","start":134597801,"end":135260467,"strand":1,"description":"EPH receptor B1 [Source:HGNC Symbol;Acc:HGNC:3392]"}, {"versioned_ensembl_gene_id":"ENSG00000244490.1","gene_symbol":"RWDD4P1","gene_name":"RWD domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23753]","synonyms":"FAM28BP","biotype":"processed_pseudogene","ncbi_id":"100419903","summary":null,"start":105301522,"end":105302086,"strand":1,"description":"RWD domain containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23753]"}, {"versioned_ensembl_gene_id":"ENSG00000273498.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789862,"end":54800938,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000089012.14","gene_symbol":"SIRPG","gene_name":"signal regulatory protein gamma [Source:HGNC Symbol;Acc:HGNC:15757]","synonyms":"SIRPB2,SIRP-B2,CD172g,bA77C3.1,SIRPgamma","biotype":"protein_coding","ncbi_id":"55423","summary":"The protein encoded by this gene is a member of the signal-regulatory protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":1629152,"end":1657779,"strand":-1,"description":"signal regulatory protein gamma [Source:HGNC Symbol;Acc:HGNC:15757]"}, {"versioned_ensembl_gene_id":"ENSG00000121351.7","gene_symbol":"IAPP","gene_name":"islet amyloid polypeptide [Source:HGNC Symbol;Acc:HGNC:5329]","synonyms":"IAP,DAP,AMYLIN","biotype":"protein_coding","ncbi_id":"3375","summary":"This gene encodes a member of the calcitonin family of peptide hormones. This hormone is released from pancreatic beta cells following food intake to regulate blood glucose levels and act as a satiation signal. Human patients with type 1 and advanced type 2 diabetes exhibit reduced levels of the encoded hormone in blood and pancreas. This protein also exhibits a bactericidal, antimicrobial activity. [provided by RefSeq, Jul 2016]","start":21354959,"end":21379978,"strand":1,"description":"islet amyloid polypeptide [Source:HGNC Symbol;Acc:HGNC:5329]"}, {"versioned_ensembl_gene_id":"ENSG00000199334.1","gene_symbol":"RNA5S11","gene_name":"RNA, 5S ribosomal 11 [Source:HGNC Symbol;Acc:HGNC:34372]","synonyms":"RN5S11","biotype":"rRNA","ncbi_id":"100169762","summary":null,"start":228632631,"end":228632749,"strand":-1,"description":"RNA, 5S ribosomal 11 [Source:HGNC Symbol;Acc:HGNC:34372]"}, {"versioned_ensembl_gene_id":"ENSG00000275596.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5,KIR2DL5,CD158F,KIR2DL5.1,CD158F,KIR2DL5.1","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819506,"end":54828970,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000227479.1","gene_symbol":"AC124861.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":240227560,"end":240256035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213940.4","gene_symbol":"AC026477.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53206561,"end":53207176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225775.1","gene_symbol":"AL137220.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9124221,"end":9161777,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169814.12","gene_symbol":"BTD","gene_name":"biotinidase [Source:HGNC Symbol;Acc:HGNC:1122]","synonyms":null,"biotype":"protein_coding","ncbi_id":"686","summary":"The protein encoded by this gene functions to recycle protein-bound biotin by cleaving biocytin (biotin-epsilon-lysine), a normal product of carboxylase degradation, resulting in regeneration of free biotin. The encoded protein has also been shown to have biotinyl transferase activity. Mutations in this gene are associated with biotinidase deficiency. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Aug 2013]","start":15601341,"end":15645822,"strand":1,"description":"biotinidase [Source:HGNC Symbol;Acc:HGNC:1122]"}, {"versioned_ensembl_gene_id":"ENSG00000184995.7","gene_symbol":"IFNE","gene_name":"interferon epsilon [Source:HGNC Symbol;Acc:HGNC:18163]","synonyms":"IFNE1","biotype":"protein_coding","ncbi_id":"338376","summary":null,"start":21480839,"end":21482313,"strand":-1,"description":"interferon epsilon [Source:HGNC Symbol;Acc:HGNC:18163]"}, {"versioned_ensembl_gene_id":"ENSG00000253926.1","gene_symbol":"AC011257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129415949,"end":129445852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198959.11","gene_symbol":"TGM2","gene_name":"transglutaminase 2 [Source:HGNC Symbol;Acc:HGNC:11778]","synonyms":"TGC","biotype":"protein_coding","ncbi_id":"7052","summary":"Transglutaminases are enzymes that catalyze the crosslinking of proteins by epsilon-gamma glutamyl lysine isopeptide bonds. While the primary structure of transglutaminases is not conserved, they all have the same amino acid sequence at their active sites and their activity is calcium-dependent. The protein encoded by this gene acts as a monomer, is induced by retinoic acid, and appears to be involved in apoptosis. Finally, the encoded protein is the autoantigen implicated in celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":38127387,"end":38166578,"strand":-1,"description":"transglutaminase 2 [Source:HGNC Symbol;Acc:HGNC:11778]"}, {"versioned_ensembl_gene_id":"ENSG00000183169.6","gene_symbol":"POM121L1P","gene_name":"POM121 transmembrane nucleoporin like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:16439]","synonyms":"POM121L1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"25812","summary":"This locus appears to be a pseudogene related to DKFZp434K191, which is of unknown function. This pseudogene lies in the immunoglobulin lambda gene cluster on chromosome 22q11.21. [provided by RefSeq, Jul 2008]","start":22639177,"end":22644473,"strand":-1,"description":"POM121 transmembrane nucleoporin like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:16439]"}, {"versioned_ensembl_gene_id":"ENSG00000147144.12","gene_symbol":"CCDC120","gene_name":"coiled-coil domain containing 120 [Source:HGNC Symbol;Acc:HGNC:28910]","synonyms":"JM11","biotype":"protein_coding","ncbi_id":"90060","summary":"This gene encodes a protein that contains a coiled-coil domain. Several alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Nov 2012]","start":49053572,"end":49069857,"strand":1,"description":"coiled-coil domain containing 120 [Source:HGNC Symbol;Acc:HGNC:28910]"}, {"versioned_ensembl_gene_id":"ENSG00000259570.1","gene_symbol":"AC243562.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84394512,"end":84395514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237928.5","gene_symbol":"NFIA-AS2","gene_name":"NFIA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40401]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996570","summary":null,"start":60940239,"end":60970776,"strand":-1,"description":"NFIA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40401]"}, {"versioned_ensembl_gene_id":"ENSG00000161911.11","gene_symbol":"TREML1","gene_name":"triggering receptor expressed on myeloid cells like 1 [Source:HGNC Symbol;Acc:HGNC:20434]","synonyms":"TLT1,dJ238O23.3","biotype":"protein_coding","ncbi_id":"340205","summary":"This gene encodes a member of the triggering receptor expressed on myeloid cells-like (TREM) family. The encoded protein is a type 1 single Ig domain orphan receptor localized to the alpha-granule membranes of platelets. The encoded protein is involved in platelet aggregation, inflammation, and cellular activation and has been linked to Gray platelet syndrome. Alternative splicing results in multiple transcript variants [provided by RefSeq, Nov 2012]","start":41149342,"end":41154337,"strand":-1,"description":"triggering receptor expressed on myeloid cells like 1 [Source:HGNC Symbol;Acc:HGNC:20434]"}, {"versioned_ensembl_gene_id":"ENSG00000237550.5","gene_symbol":"RPL9P9","gene_name":"ribosomal protein L9 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17251]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":82372196,"end":82372912,"strand":-1,"description":"ribosomal protein L9 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17251]"}, {"versioned_ensembl_gene_id":"ENSG00000154582.16","gene_symbol":"ELOC","gene_name":"elongin C [Source:HGNC Symbol;Acc:HGNC:11617]","synonyms":"TCEB1,SIII","biotype":"protein_coding","ncbi_id":"6921","summary":"This gene encodes the protein elongin C, which is a subunit of the transcription factor B (SIII) complex. The SIII complex is composed of elongins A/A2, B and C. It activates elongation by RNA polymerase II by suppressing transient pausing of the polymerase at many sites within transcription units. Elongin A functions as the transcriptionally active component of the SIII complex, whereas elongins B and C are regulatory subunits. Elongin A2 is specifically expressed in the testis, and capable of forming a stable complex with elongins B and C. The von Hippel-Lindau tumor suppressor protein binds to elongins B and C, and thereby inhibits transcription elongation. Multiple alternatively spliced transcript variants encoding two distinct isoforms have been identified. [provided by RefSeq, Mar 2011]","start":73939169,"end":73972287,"strand":-1,"description":"elongin C [Source:HGNC Symbol;Acc:HGNC:11617]"}, {"versioned_ensembl_gene_id":"ENSG00000120242.3","gene_symbol":"IFNA8","gene_name":"interferon alpha 8 [Source:HGNC Symbol;Acc:HGNC:5429]","synonyms":"IFN-alphaB","biotype":"protein_coding","ncbi_id":"3445","summary":null,"start":21409147,"end":21410185,"strand":1,"description":"interferon alpha 8 [Source:HGNC Symbol;Acc:HGNC:5429]"}, {"versioned_ensembl_gene_id":"ENSG00000185670.7","gene_symbol":"ZBTB3","gene_name":"zinc finger and BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22918]","synonyms":"FLJ23392","biotype":"protein_coding","ncbi_id":"79842","summary":null,"start":62748319,"end":62754188,"strand":-1,"description":"zinc finger and BTB domain containing 3 [Source:HGNC Symbol;Acc:HGNC:22918]"}, {"versioned_ensembl_gene_id":"ENSG00000261696.1","gene_symbol":"AL353732.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21394888,"end":21396346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231195.1","gene_symbol":"IFNA11P","gene_name":"interferon alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:5442]","synonyms":"IFNP11","biotype":"unprocessed_pseudogene","ncbi_id":"3461","summary":null,"start":21398614,"end":21399139,"strand":-1,"description":"interferon alpha 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:5442]"}, {"versioned_ensembl_gene_id":"ENSG00000272149.1","gene_symbol":"AC112211.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33144104,"end":33147721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269458.1","gene_symbol":"AC022145.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22925377,"end":22925547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277151.1","gene_symbol":"AL138820.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32782874,"end":32788178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198822.10","gene_symbol":"GRM3","gene_name":"glutamate metabotropic receptor 3 [Source:HGNC Symbol;Acc:HGNC:4595]","synonyms":"MGLUR3,mGlu3,GPRC1C","biotype":"protein_coding","ncbi_id":"2913","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. [provided by RefSeq, Jul 2008]","start":86643914,"end":86864884,"strand":1,"description":"glutamate metabotropic receptor 3 [Source:HGNC Symbol;Acc:HGNC:4595]"}, {"versioned_ensembl_gene_id":"ENSG00000273329.1","gene_symbol":"AC078846.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129604548,"end":129611630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184206.11","gene_symbol":"GOLGA6L4","gene_name":"golgin A6 family-like 4 [Source:HGNC Symbol;Acc:HGNC:27256]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643707","summary":null,"start":84235773,"end":84245368,"strand":1,"description":"golgin A6 family-like 4 [Source:HGNC Symbol;Acc:HGNC:27256]"}, {"versioned_ensembl_gene_id":"ENSG00000119041.10","gene_symbol":"GTF3C3","gene_name":"general transcription factor IIIC subunit 3 [Source:HGNC Symbol;Acc:HGNC:4666]","synonyms":"TFiiiC2-102,TFIIIC102","biotype":"protein_coding","ncbi_id":"9330","summary":"The protein encoded by this gene is part of the TFIIIC2 complex, which binds to the promoters of small nuclear and cytoplasmic RNA genes in order to recruit RNA polymerase III. The TFIIIC2 complex is composed of six subunits. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":196763032,"end":196799725,"strand":-1,"description":"general transcription factor IIIC subunit 3 [Source:HGNC Symbol;Acc:HGNC:4666]"}, {"versioned_ensembl_gene_id":"ENSG00000238197.5","gene_symbol":"PAXBP1-AS1","gene_name":"PAXBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39603]","synonyms":"GCFC1-AS1","biotype":"antisense_RNA","ncbi_id":"100506215","summary":null,"start":32728115,"end":32743122,"strand":1,"description":"PAXBP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39603]"}, {"versioned_ensembl_gene_id":"ENSG00000271573.1","gene_symbol":"AL136982.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87027184,"end":87027477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166483.10","gene_symbol":"WEE1","gene_name":"WEE1 G2 checkpoint kinase [Source:HGNC Symbol;Acc:HGNC:12761]","synonyms":"WEE1A","biotype":"protein_coding","ncbi_id":"7465","summary":"This gene encodes a nuclear protein, which is a tyrosine kinase belonging to the Ser/Thr family of protein kinases. This protein catalyzes the inhibitory tyrosine phosphorylation of CDC2/cyclin B kinase, and appears to coordinate the transition between DNA replication and mitosis by protecting the nucleus from cytoplasmically activated CDC2 kinase. [provided by RefSeq, Jul 2008]","start":9573681,"end":9593457,"strand":1,"description":"WEE1 G2 checkpoint kinase [Source:HGNC Symbol;Acc:HGNC:12761]"}, {"versioned_ensembl_gene_id":"ENSG00000182083.7","gene_symbol":"OR6B2","gene_name":"olfactory receptor family 6 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:15041]","synonyms":"OR6B2P","biotype":"protein_coding","ncbi_id":"389090","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":240028965,"end":240030456,"strand":-1,"description":"olfactory receptor family 6 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:15041]"}, {"versioned_ensembl_gene_id":"ENSG00000260615.1","gene_symbol":"RPL23AP97","gene_name":"ribosomal protein L23a pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:51632]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723647","summary":null,"start":114346167,"end":114346637,"strand":1,"description":"ribosomal protein L23a pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:51632]"}, {"versioned_ensembl_gene_id":"ENSG00000111971.14","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31667433,"end":31674786,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000234829.4","gene_symbol":"IFNA17","gene_name":"interferon alpha 17 [Source:HGNC Symbol;Acc:HGNC:5422]","synonyms":"LEIF2C1,IFN-alphaI","biotype":"protein_coding","ncbi_id":"3451","summary":null,"start":21227243,"end":21228222,"strand":-1,"description":"interferon alpha 17 [Source:HGNC Symbol;Acc:HGNC:5422]"}, {"versioned_ensembl_gene_id":"ENSG00000129194.7","gene_symbol":"SOX15","gene_name":"SRY-box 15 [Source:HGNC Symbol;Acc:HGNC:11196]","synonyms":"SOX27,SOX26,SOX20","biotype":"protein_coding","ncbi_id":"6665","summary":"This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. [provided by RefSeq, Jul 2008]","start":7588178,"end":7590170,"strand":-1,"description":"SRY-box 15 [Source:HGNC Symbol;Acc:HGNC:11196]"}, {"versioned_ensembl_gene_id":"ENSG00000141655.16","gene_symbol":"TNFRSF11A","gene_name":"TNF receptor superfamily member 11a [Source:HGNC Symbol;Acc:HGNC:11908]","synonyms":"CD265,RANK,PDB2,LOH18CR1,FEO","biotype":"protein_coding","ncbi_id":"8792","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptors can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. This receptor and its ligand are important regulators of the interaction between T cells and dendritic cells. This receptor is also an essential mediator for osteoclast and lymph node development. Mutations at this locus have been associated with familial expansile osteolysis, autosomal recessive osteopetrosis, and Paget disease of bone. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2012]","start":62325287,"end":62391292,"strand":1,"description":"TNF receptor superfamily member 11a [Source:HGNC Symbol;Acc:HGNC:11908]"}, {"versioned_ensembl_gene_id":"ENSG00000284428.1","gene_symbol":"AC092329.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23259906,"end":23274251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268469.1","gene_symbol":"BNIP3P38","gene_name":"BCL2 interacting protein 3 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:49718]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421709","summary":null,"start":23236308,"end":23236851,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:49718]"}, {"versioned_ensembl_gene_id":"ENSG00000230082.1","gene_symbol":"PRRT3-AS1","gene_name":"PRRT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41151]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874032","summary":null,"start":9947404,"end":9954787,"strand":1,"description":"PRRT3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41151]"}, {"versioned_ensembl_gene_id":"ENSG00000231066.3","gene_symbol":"NPM1P9","gene_name":"nucleophosmin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:7929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392428","summary":null,"start":14834476,"end":14835319,"strand":-1,"description":"nucleophosmin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:7929]"}, {"versioned_ensembl_gene_id":"ENSG00000189350.12","gene_symbol":"TOGARAM2","gene_name":"TOG array regulator of axonemal microtubules 2 [Source:HGNC Symbol;Acc:HGNC:33715]","synonyms":"Crescerin-2,LOC165186,FLJ43249,FAM179A","biotype":"protein_coding","ncbi_id":"165186","summary":null,"start":28956611,"end":29061373,"strand":1,"description":"TOG array regulator of axonemal microtubules 2 [Source:HGNC Symbol;Acc:HGNC:33715]"}, {"versioned_ensembl_gene_id":"ENSG00000103184.11","gene_symbol":"SEC14L5","gene_name":"SEC14 like lipid binding 5 [Source:HGNC Symbol;Acc:HGNC:29032]","synonyms":"PRELID4B,KIAA0420","biotype":"protein_coding","ncbi_id":"9717","summary":null,"start":4958317,"end":5019158,"strand":1,"description":"SEC14 like lipid binding 5 [Source:HGNC Symbol;Acc:HGNC:29032]"}, {"versioned_ensembl_gene_id":"ENSG00000129757.12","gene_symbol":"CDKN1C","gene_name":"cyclin dependent kinase inhibitor 1C [Source:HGNC Symbol;Acc:HGNC:1786]","synonyms":"BWS,BWCR,P57,KIP2","biotype":"protein_coding","ncbi_id":"1028","summary":"This gene is imprinted, with preferential expression of the maternal allele. The encoded protein is a tight-binding, strong inhibitor of several G1 cyclin/Cdk complexes and a negative regulator of cell proliferation. Mutations in this gene are implicated in sporadic cancers and Beckwith-Wiedemann syndorome, suggesting that this gene is a tumor suppressor candidate. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":2883213,"end":2885881,"strand":-1,"description":"cyclin dependent kinase inhibitor 1C [Source:HGNC Symbol;Acc:HGNC:1786]"}, {"versioned_ensembl_gene_id":"ENSG00000206504.2","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"PERB11,HCGIX,HCGIX4,HCGIX-4","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29964492,"end":29967793,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000227936.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33052792,"end":33064929,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000064999.13","gene_symbol":"ANKS1A","gene_name":"ankyrin repeat and sterile alpha motif domain containing 1A [Source:HGNC Symbol;Acc:HGNC:20961]","synonyms":"KIAA0229,ANKS1","biotype":"protein_coding","ncbi_id":"23294","summary":null,"start":34889265,"end":35091413,"strand":1,"description":"ankyrin repeat and sterile alpha motif domain containing 1A [Source:HGNC Symbol;Acc:HGNC:20961]"}, {"versioned_ensembl_gene_id":"ENSG00000278545.4","gene_symbol":"MARCH8","gene_name":"membrane associated ring-CH-type finger 8 [Source:HGNC Symbol;Acc:HGNC:23356]","synonyms":"RNF178,MIR,MARCH-VIII,CMIR,c-MIR","biotype":"protein_coding","ncbi_id":"220972","summary":"MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010]","start":45470650,"end":45480390,"strand":-1,"description":"membrane associated ring-CH-type finger 8 [Source:HGNC Symbol;Acc:HGNC:23356]"}, {"versioned_ensembl_gene_id":"ENSG00000259814.1","gene_symbol":"AC102941.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29609676,"end":29611212,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125356.6","gene_symbol":"NDUFA1","gene_name":"NADH:ubiquinone oxidoreductase subunit A1 [Source:HGNC Symbol;Acc:HGNC:7683]","synonyms":"MWFE,CI-MWFE","biotype":"protein_coding","ncbi_id":"4694","summary":"The human NDUFA1 gene codes for an essential component of complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone. It has been noted that the N-terminal hydrophobic domain has the potential to be folded into an alpha-helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular subunits of complex I. The highly conserved two-domain structure suggests that this feature is critical for the protein function and might act as an anchor for the NADH:ubiquinone oxidoreductase complex at the inner mitochondrial membrane. However, the NDUFA1 peptide is one of about 31 components of the \"hydrophobic protein\" (HP) fraction of complex I which is involved in proton translocation. Thus the NDUFA1 peptide may also participate in that function. [provided by RefSeq, Jul 2008]","start":119871487,"end":119876662,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A1 [Source:HGNC Symbol;Acc:HGNC:7683]"}, {"versioned_ensembl_gene_id":"ENSG00000224217.1","gene_symbol":"BX119904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116748530,"end":116748877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275980.1","gene_symbol":"AL390882.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21135598,"end":21136350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223536.5","gene_symbol":"AC008164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16728124,"end":16767555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214783.9","gene_symbol":"POLR2J4","gene_name":"RNA polymerase II subunit J4, pseudogene [Source:HGNC Symbol;Acc:HGNC:28195]","synonyms":"MGC13098,MGC13098","biotype":"processed_transcript","ncbi_id":"84820","summary":null,"start":43940895,"end":44019175,"strand":-1,"description":"RNA polymerase II subunit J4, pseudogene [Source:HGNC Symbol;Acc:HGNC:28195]"}, {"versioned_ensembl_gene_id":"ENSG00000232814.2","gene_symbol":"COL4A2-AS1","gene_name":"COL4A2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40156]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874203","summary":null,"start":110502575,"end":110508179,"strand":-1,"description":"COL4A2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40156]"}, {"versioned_ensembl_gene_id":"ENSG00000102981.9","gene_symbol":"PARD6A","gene_name":"par-6 family cell polarity regulator alpha [Source:HGNC Symbol;Acc:HGNC:15943]","synonyms":"PAR-6A,PAR-6,TIP-40,TAX40,PAR6alpha","biotype":"protein_coding","ncbi_id":"50855","summary":"This gene is a member of the PAR6 family and encodes a protein with a PSD95/Discs-large/ZO1 (PDZ) domain and a semi-Cdc42/Rac interactive binding (CRIB) domain. This cell membrane protein is involved in asymmetrical cell division and cell polarization processes as a member of a multi-protein complex. The protein also has a role in the epithelial-to-mesenchymal transition (EMT) that characterizes the invasive phenotype associated with metastatic carcinomas. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":67660946,"end":67662778,"strand":1,"description":"par-6 family cell polarity regulator alpha [Source:HGNC Symbol;Acc:HGNC:15943]"}, {"versioned_ensembl_gene_id":"ENSG00000281179.1","gene_symbol":"AC135068.8","gene_name":null,"synonyms":null,"biotype":"IG_V_gene","ncbi_id":null,"summary":null,"start":21717808,"end":21718245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235920.1","gene_symbol":"AC073109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11820317,"end":11821294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242227.6","gene_symbol":"HLA-L","gene_name":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]","synonyms":"HLAL,HLA92,HLA-92","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3139","summary":null,"start":30249542,"end":30256896,"strand":1,"description":"major histocompatibility complex, class I, L (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4970]"}, {"versioned_ensembl_gene_id":"ENSG00000171855.6","gene_symbol":"IFNB1","gene_name":"interferon beta 1 [Source:HGNC Symbol;Acc:HGNC:5434]","synonyms":"IFNB,IFF,IFB","biotype":"protein_coding","ncbi_id":"3456","summary":"This gene encodes a cytokine that belongs to the interferon family of signaling proteins, which are released as part of the innate immune response to pathogens. The protein encoded by this gene belongs to the type I class of interferons, which are important for defense against viral infections. In addition, type I interferons are involved in cell differentiation and anti-tumor defenses. Following secretion in response to a pathogen, type I interferons bind a homologous receptor complex and induce transcription of genes such as those encoding inflammatory cytokines and chemokines. Overactivation of type I interferon secretion is linked to autoimmune diseases. Mice deficient for this gene display several phenotypes including defects in B cell maturation and increased susceptibility to viral infection. [provided by RefSeq, Sep 2015]","start":21077105,"end":21077963,"strand":-1,"description":"interferon beta 1 [Source:HGNC Symbol;Acc:HGNC:5434]"}, {"versioned_ensembl_gene_id":"ENSG00000185686.17","gene_symbol":"PRAME","gene_name":"preferentially expressed antigen in melanoma [Source:HGNC Symbol;Acc:HGNC:9336]","synonyms":"MAPE,CT130","biotype":"protein_coding","ncbi_id":"23532","summary":"This gene encodes an antigen that is preferentially expressed in human melanomas and that is recognized by cytolytic T lymphocytes. It is not expressed in normal tissues, except testis. The encoded protein acts as a repressor of retinoic acid receptor, and likely confers a growth advantage to cancer cells via this function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":22547701,"end":22559361,"strand":-1,"description":"preferentially expressed antigen in melanoma [Source:HGNC Symbol;Acc:HGNC:9336]"}, {"versioned_ensembl_gene_id":"ENSG00000227356.2","gene_symbol":"LINC00866","gene_name":"long intergenic non-protein coding RNA 866 [Source:HGNC Symbol;Acc:HGNC:45232]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505561","summary":null,"start":97828478,"end":97849798,"strand":-1,"description":"long intergenic non-protein coding RNA 866 [Source:HGNC Symbol;Acc:HGNC:45232]"}, {"versioned_ensembl_gene_id":"ENSG00000252249.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":93879106,"end":93879229,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000243789.10","gene_symbol":"JMJD7","gene_name":"jumonji domain containing 7 [Source:HGNC Symbol;Acc:HGNC:34397]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100137047","summary":"This gene encodes a highly conserved protein with a JmjC domain, which are part of the cupin metalloenzyme superfamily. JmjC proteins may function as 2-oxoglutarate-Fe(II)-dependent dioxygenases. Most tissues also express read-through transcripts from this gene into the downstream phospholipase A2, group IVB (cytosolic) gene, some of which may encode fusion proteins combining the N-terminus of this protein with the phospholipase A2, group IVB protein. [provided by RefSeq, Jul 2008]","start":41828085,"end":41837581,"strand":1,"description":"jumonji domain containing 7 [Source:HGNC Symbol;Acc:HGNC:34397]"}, {"versioned_ensembl_gene_id":"ENSG00000236759.7","gene_symbol":"EHMT2","gene_name":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]","synonyms":"G9A,NG36/G9a,BAT8,Em:AF134726.3,KMT1C,C6orf30","biotype":"protein_coding","ncbi_id":"10919","summary":"This gene encodes a methyltransferase that methylates lysine residues of histone H3. Methylation of H3 at lysine 9 by this protein results in recruitment of additional epigenetic regulators and repression of transcription. This gene was initially thought to be two different genes, NG36 and G9a, adjacent to each other in the HLA locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":31867303,"end":31885231,"strand":-1,"description":"euchromatic histone lysine methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14129]"}, {"versioned_ensembl_gene_id":"ENSG00000250492.1","gene_symbol":"INTS6P1","gene_name":"integrator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"285634","summary":null,"start":39718984,"end":39721513,"strand":-1,"description":"integrator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43921]"}, {"versioned_ensembl_gene_id":"ENSG00000078967.12","gene_symbol":"UBE2D4","gene_name":"ubiquitin conjugating enzyme E2 D4 (putative) [Source:HGNC Symbol;Acc:HGNC:21647]","synonyms":"HBUCE1","biotype":"protein_coding","ncbi_id":"51619","summary":null,"start":43926438,"end":43956136,"strand":1,"description":"ubiquitin conjugating enzyme E2 D4 (putative) [Source:HGNC Symbol;Acc:HGNC:21647]"}, {"versioned_ensembl_gene_id":"ENSG00000219481.10","gene_symbol":"NBPF1","gene_name":"NBPF member 1 [Source:HGNC Symbol;Acc:HGNC:26088]","synonyms":"KIAA1693,FLJ20719","biotype":"protein_coding","ncbi_id":"55672","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2013]","start":16562319,"end":16613562,"strand":-1,"description":"NBPF member 1 [Source:HGNC Symbol;Acc:HGNC:26088]"}, {"versioned_ensembl_gene_id":"ENSG00000245468.3","gene_symbol":"LINC02447","gene_name":"long intergenic non-protein coding RNA 2447 [Source:HGNC Symbol;Acc:HGNC:53379]","synonyms":null,"biotype":"lincRNA","ncbi_id":"730971","summary":null,"start":7094571,"end":7103385,"strand":-1,"description":"long intergenic non-protein coding RNA 2447 [Source:HGNC Symbol;Acc:HGNC:53379]"}, {"versioned_ensembl_gene_id":"ENSG00000230119.1","gene_symbol":"AC123900.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33190233,"end":33190328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258476.5","gene_symbol":"LINC02207","gene_name":"long intergenic non-protein coding RNA 2207 [Source:HGNC Symbol;Acc:HGNC:53073]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927153","summary":null,"start":93863109,"end":93878356,"strand":1,"description":"long intergenic non-protein coding RNA 2207 [Source:HGNC Symbol;Acc:HGNC:53073]"}, {"versioned_ensembl_gene_id":"ENSG00000155111.14","gene_symbol":"CDK19","gene_name":"cyclin dependent kinase 19 [Source:HGNC Symbol;Acc:HGNC:19338]","synonyms":"CDC2L6,bA346C16.3,KIAA1028,CDK11","biotype":"protein_coding","ncbi_id":"23097","summary":"This gene encodes a protein that is one of the components of the Mediator co-activator complex. The Mediator complex is a multi-protein complex required for transcriptional activation by DNA binding transcription factors of genes transcribed by RNA polymerase II. The protein encoded by this gene is similar to cyclin-dependent kinase 8 which can also be a component of the Mediator complex. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":110609978,"end":110815958,"strand":-1,"description":"cyclin dependent kinase 19 [Source:HGNC Symbol;Acc:HGNC:19338]"}, {"versioned_ensembl_gene_id":"ENSG00000174173.6","gene_symbol":"TRMT10C","gene_name":"tRNA methyltransferase 10C, mitochondrial RNase P subunit [Source:HGNC Symbol;Acc:HGNC:26022]","synonyms":"RG9MTD1,MRPP1,FLJ20432","biotype":"protein_coding","ncbi_id":"54931","summary":"This gene encodes the precursor of a subunit of the mitochondrial ribonuclease P, which is involved in 5' processing of mitochondrial tRNAs. The encoded protein may confer RNA-binding capacity to mitochondrial ribonuclease P and may be essential for transcript processing, RNA modification, translation and mitochondrial respiration. [provided by RefSeq, Nov 2012]","start":101561862,"end":101566446,"strand":1,"description":"tRNA methyltransferase 10C, mitochondrial RNase P subunit [Source:HGNC Symbol;Acc:HGNC:26022]"}, {"versioned_ensembl_gene_id":"ENSG00000261615.6","gene_symbol":"LINC01858","gene_name":"long intergenic non-protein coding RNA 1858 [Source:HGNC Symbol;Acc:HGNC:52676]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929144","summary":null,"start":23046958,"end":23061752,"strand":-1,"description":"long intergenic non-protein coding RNA 1858 [Source:HGNC Symbol;Acc:HGNC:52676]"}, {"versioned_ensembl_gene_id":"ENSG00000281060.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195740223,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000049768.14","gene_symbol":"FOXP3","gene_name":"forkhead box P3 [Source:HGNC Symbol;Acc:HGNC:6106]","synonyms":"JM2,IPEX,DIETER,AIID,XPID,SCURFIN,PIDX","biotype":"protein_coding","ncbi_id":"50943","summary":"The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":49250436,"end":49264826,"strand":-1,"description":"forkhead box P3 [Source:HGNC Symbol;Acc:HGNC:6106]"}, {"versioned_ensembl_gene_id":"ENSG00000231371.1","gene_symbol":"AKR1B1P8","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33496]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392525","summary":null,"start":116043483,"end":116044418,"strand":1,"description":"aldo-keto reductase family 1 member B1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:33496]"}, {"versioned_ensembl_gene_id":"ENSG00000187808.4","gene_symbol":"SOWAHD","gene_name":"sosondowah ankyrin repeat domain family member D [Source:HGNC Symbol;Acc:HGNC:32960]","synonyms":"ANKRD58","biotype":"protein_coding","ncbi_id":"347454","summary":null,"start":119758613,"end":119760164,"strand":1,"description":"sosondowah ankyrin repeat domain family member D [Source:HGNC Symbol;Acc:HGNC:32960]"}, {"versioned_ensembl_gene_id":"ENSG00000279601.1","gene_symbol":"AC005052.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":119693568,"end":119696059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275430.3","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"FLJ14408,KIAA1359","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195721575,"end":195741387,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000163214.20","gene_symbol":"DHX57","gene_name":"DExH-box helicase 57 [Source:HGNC Symbol;Acc:HGNC:20086]","synonyms":"DDX57","biotype":"protein_coding","ncbi_id":"90957","summary":null,"start":38797729,"end":38875934,"strand":-1,"description":"DExH-box helicase 57 [Source:HGNC Symbol;Acc:HGNC:20086]"}, {"versioned_ensembl_gene_id":"ENSG00000234785.1","gene_symbol":"EEF1GP5","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642357","summary":null,"start":115702811,"end":115704120,"strand":1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44560]"}, {"versioned_ensembl_gene_id":"ENSG00000278427.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54802842,"end":54817184,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000122299.11","gene_symbol":"ZC3H7A","gene_name":"zinc finger CCCH-type containing 7A [Source:HGNC Symbol;Acc:HGNC:30959]","synonyms":"ZC3H7,HSPC055,FLJ20318,ZC3HDC7","biotype":"protein_coding","ncbi_id":"29066","summary":null,"start":11750586,"end":11797267,"strand":-1,"description":"zinc finger CCCH-type containing 7A [Source:HGNC Symbol;Acc:HGNC:30959]"}, {"versioned_ensembl_gene_id":"ENSG00000174032.16","gene_symbol":"SLC25A30","gene_name":"solute carrier family 25 member 30 [Source:HGNC Symbol;Acc:HGNC:27371]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253512","summary":"Although the outer mitochondrial membrane is permeable to many small metabolites, transport of solutes across the inner mitochondrial membrane is achieved by members of the mitochondrial carrier protein family, such as SLC25A30 (Haguenauer et al., 2005 [PubMed 15809292]).[supplied by OMIM, Mar 2008]","start":45393316,"end":45418455,"strand":-1,"description":"solute carrier family 25 member 30 [Source:HGNC Symbol;Acc:HGNC:27371]"}, {"versioned_ensembl_gene_id":"ENSG00000273149.1","gene_symbol":"AL138963.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45340039,"end":45341183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185002.9","gene_symbol":"RFX6","gene_name":"regulatory factor X6 [Source:HGNC Symbol;Acc:HGNC:21478]","synonyms":"RFXDC1,MGC33442,dJ955L16.1","biotype":"protein_coding","ncbi_id":"222546","summary":"The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.[provided by RefSeq, Sep 2010]","start":116877212,"end":116932163,"strand":1,"description":"regulatory factor X6 [Source:HGNC Symbol;Acc:HGNC:21478]"}, {"versioned_ensembl_gene_id":"ENSG00000282946.1","gene_symbol":"AC018558.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35528367,"end":35529318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231684.3","gene_symbol":"EIF1P3","gene_name":"eukaryotic translation initiation factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49616]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730144","summary":null,"start":182336001,"end":182336334,"strand":1,"description":"eukaryotic translation initiation factor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49616]"}, {"versioned_ensembl_gene_id":"ENSG00000114956.19","gene_symbol":"DGUOK","gene_name":"deoxyguanosine kinase [Source:HGNC Symbol;Acc:HGNC:2858]","synonyms":"dGK","biotype":"protein_coding","ncbi_id":"1716","summary":"In mammalian cells, the phosphorylation of purine deoxyribonucleosides is mediated predominantly by two deoxyribonucleoside kinases, cytosolic deoxycytidine kinase and mitochondrial deoxyguanosine kinase. The protein encoded by this gene is responsible for phosphorylation of purine deoxyribonucleosides in the mitochondrial matrix. In addition, this protein phosphorylates several purine deoxyribonucleoside analogs used in the treatment of lymphoproliferative disorders, and this phosphorylation is critical for the effectiveness of the analogs. Alternative splice variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":73926826,"end":73958961,"strand":1,"description":"deoxyguanosine kinase [Source:HGNC Symbol;Acc:HGNC:2858]"}, {"versioned_ensembl_gene_id":"ENSG00000269743.2","gene_symbol":"SLC25A53","gene_name":"solute carrier family 25 member 53 [Source:HGNC Symbol;Acc:HGNC:31894]","synonyms":"MCART6","biotype":"protein_coding","ncbi_id":"401612","summary":null,"start":104099214,"end":104157027,"strand":-1,"description":"solute carrier family 25 member 53 [Source:HGNC Symbol;Acc:HGNC:31894]"}, {"versioned_ensembl_gene_id":"ENSG00000232096.1","gene_symbol":"YPEL5P1","gene_name":"YPEL5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50555]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130996","summary":null,"start":182182730,"end":182183096,"strand":-1,"description":"YPEL5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50555]"}, {"versioned_ensembl_gene_id":"ENSG00000162928.8","gene_symbol":"PEX13","gene_name":"peroxisomal biogenesis factor 13 [Source:HGNC Symbol;Acc:HGNC:8855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5194","summary":"This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]","start":61017225,"end":61051990,"strand":1,"description":"peroxisomal biogenesis factor 13 [Source:HGNC Symbol;Acc:HGNC:8855]"}, {"versioned_ensembl_gene_id":"ENSG00000090402.7","gene_symbol":"SI","gene_name":"sucrase-isomaltase [Source:HGNC Symbol;Acc:HGNC:10856]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6476","summary":"This gene encodes a sucrase-isomaltase enzyme that is expressed in the intestinal brush border. The encoded protein is synthesized as a precursor protein that is cleaved by pancreatic proteases into two enzymatic subunits sucrase and isomaltase. These two subunits heterodimerize to form the sucrose-isomaltase complex. This complex is essential for the digestion of dietary carbohydrates including starch, sucrose and isomaltose. Mutations in this gene are the cause of congenital sucrase-isomaltase deficiency.[provided by RefSeq, Apr 2010]","start":164978898,"end":165078495,"strand":-1,"description":"sucrase-isomaltase [Source:HGNC Symbol;Acc:HGNC:10856]"}, {"versioned_ensembl_gene_id":"ENSG00000240376.1","gene_symbol":"AC010343.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33162179,"end":33162807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250697.1","gene_symbol":"AC010343.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32925639,"end":33297910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157423.17","gene_symbol":"HYDIN","gene_name":"HYDIN, axonemal central pair apparatus protein [Source:HGNC Symbol;Acc:HGNC:19368]","synonyms":"PPP1R31,KIAA1864,DKFZp434D0513,CILD5","biotype":"protein_coding","ncbi_id":"54768","summary":"This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]","start":70807378,"end":71230722,"strand":-1,"description":"HYDIN, axonemal central pair apparatus protein [Source:HGNC Symbol;Acc:HGNC:19368]"}, {"versioned_ensembl_gene_id":"ENSG00000214946.14","gene_symbol":"TBC1D26","gene_name":"TBC1 domain family member 26 [Source:HGNC Symbol;Acc:HGNC:28745]","synonyms":"MGC51025","biotype":"protein_coding","ncbi_id":"353149","summary":null,"start":15732247,"end":15749192,"strand":1,"description":"TBC1 domain family member 26 [Source:HGNC Symbol;Acc:HGNC:28745]"}, {"versioned_ensembl_gene_id":"ENSG00000182220.14","gene_symbol":"ATP6AP2","gene_name":"ATPase H+ transporting accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:18305]","synonyms":"RENR,PRR,M8-9,ATP6M8-9,ATP6IP2,APT6M8-9","biotype":"protein_coding","ncbi_id":"10159","summary":"This gene encodes a protein that is associated with adenosine triphosphatases (ATPases). Proton-translocating ATPases have fundamental roles in energy conservation, secondary active transport, acidification of intracellular compartments, and cellular pH homeostasis. There are three classes of ATPases- F, P, and V. The vacuolar (V-type) ATPases have a transmembrane proton-conducting sector and an extramembrane catalytic sector. The encoded protein has been found associated with the transmembrane sector of the V-type ATPases. [provided by RefSeq, Jul 2008]","start":40579372,"end":40606848,"strand":1,"description":"ATPase H+ transporting accessory protein 2 [Source:HGNC Symbol;Acc:HGNC:18305]"}, {"versioned_ensembl_gene_id":"ENSG00000251443.1","gene_symbol":"LINC02160","gene_name":"long intergenic non-protein coding RNA 2160 [Source:HGNC Symbol;Acc:HGNC:53021]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374716","summary":null,"start":33229735,"end":33255553,"strand":1,"description":"long intergenic non-protein coding RNA 2160 [Source:HGNC Symbol;Acc:HGNC:53021]"}, {"versioned_ensembl_gene_id":"ENSG00000248279.5","gene_symbol":"LINC02120","gene_name":"long intergenic non-protein coding RNA 2120 [Source:HGNC Symbol;Acc:HGNC:27971]","synonyms":null,"biotype":"lincRNA","ncbi_id":"340113","summary":null,"start":32947443,"end":32962467,"strand":1,"description":"long intergenic non-protein coding RNA 2120 [Source:HGNC Symbol;Acc:HGNC:27971]"}, {"versioned_ensembl_gene_id":"ENSG00000241251.2","gene_symbol":"AC090525.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43560784,"end":43561297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224810.1","gene_symbol":"AL355482.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182062677,"end":182069253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230216.1","gene_symbol":"HSPB1P2","gene_name":"heat shock protein family B (small) member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5252]","synonyms":"HSPBL3","biotype":"processed_pseudogene","ncbi_id":"653364","summary":null,"start":49233956,"end":49234501,"strand":-1,"description":"heat shock protein family B (small) member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5252]"}, {"versioned_ensembl_gene_id":"ENSG00000116663.10","gene_symbol":"FBXO6","gene_name":"F-box protein 6 [Source:HGNC Symbol;Acc:HGNC:13585]","synonyms":"Fbx6b,FBX6,FBS2,FBG2","biotype":"protein_coding","ncbi_id":"26270","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class, and its C-terminal region is highly similar to that of rat NFB42 (neural F Box 42 kDa) which may be involved in the control of the cell cycle. [provided by RefSeq, Jul 2008]","start":11664124,"end":11674354,"strand":1,"description":"F-box protein 6 [Source:HGNC Symbol;Acc:HGNC:13585]"}, {"versioned_ensembl_gene_id":"ENSG00000276952.1","gene_symbol":"AL121772.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25284915,"end":25285588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143167.11","gene_symbol":"GPA33","gene_name":"glycoprotein A33 [Source:HGNC Symbol;Acc:HGNC:4445]","synonyms":"A33","biotype":"protein_coding","ncbi_id":"10223","summary":"The glycoprotein encoded by this gene is a cell surface antigen that is expressed in greater than 95% of human colon cancers. The open reading frame encodes a 319-amino acid polypeptide having a putative secretory signal sequence and 3 potential glycosylation sites. The predicted mature protein has a 213-amino acid extracellular region, a single transmembrane domain, and a 62-amino acid intracellular tail. The sequence of the extracellular region contains 2 domains characteristic of the CD2 subgroup of the immunoglobulin (Ig) superfamily. [provided by RefSeq, Jul 2008]","start":167052836,"end":167166479,"strand":-1,"description":"glycoprotein A33 [Source:HGNC Symbol;Acc:HGNC:4445]"}, {"versioned_ensembl_gene_id":"ENSG00000236120.6","gene_symbol":"AC110995.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5653421,"end":5726305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255983.1","gene_symbol":"AC007848.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5388589,"end":5406651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280961.1","gene_symbol":"TTTY3B","gene_name":"testis-specific transcript, Y-linked 3B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31888]","synonyms":"LNCRNA00122","biotype":"lincRNA","ncbi_id":"474148","summary":"There are two copies of this gene within the P1 palindrome on chromosome Y. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":23936727,"end":23941622,"strand":-1,"description":"testis-specific transcript, Y-linked 3B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31888]"}, {"versioned_ensembl_gene_id":"ENSG00000226369.1","gene_symbol":"USP9YP11","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:38460]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421224","summary":null,"start":23934953,"end":23940101,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:38460]"}, {"versioned_ensembl_gene_id":"ENSG00000198842.9","gene_symbol":"DUSP27","gene_name":"dual specificity phosphatase 27 (putative) [Source:HGNC Symbol;Acc:HGNC:25034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92235","summary":null,"start":167094045,"end":167129165,"strand":1,"description":"dual specificity phosphatase 27 (putative) [Source:HGNC Symbol;Acc:HGNC:25034]"}, {"versioned_ensembl_gene_id":"ENSG00000007264.14","gene_symbol":"MATK","gene_name":"megakaryocyte-associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6906]","synonyms":"MGC2101,MGC1708,Lsk,HYLTK,HYL,HHYLTK,DKFZp434N1212,CTK,CHK","biotype":"protein_coding","ncbi_id":"4145","summary":"The protein encoded by this gene has amino acid sequence similarity to Csk tyrosine kinase and has the structural features of the CSK subfamily: SRC homology SH2 and SH3 domains, a catalytic domain, a unique N terminus, lack of myristylation signals, lack of a negative regulatory phosphorylation site, and lack of an autophosphorylation site. This protein is thought to play a significant role in the signal transduction of hematopoietic cells. It is able to phosphorylate and inactivate Src family kinases, and may play an inhibitory role in the control of T-cell proliferation. This protein might be involved in signaling in some cases of breast cancer. Three alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":3777970,"end":3802129,"strand":-1,"description":"megakaryocyte-associated tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:6906]"}, {"versioned_ensembl_gene_id":"ENSG00000269226.7","gene_symbol":"TMSB15B","gene_name":"thymosin beta 15B [Source:NCBI gene;Acc:286527]","synonyms":"MGC39900,Tbeta15b","biotype":"protein_coding","ncbi_id":"286527","summary":null,"start":104063871,"end":104076212,"strand":-1,"description":"thymosin beta 15B [Source:NCBI gene;Acc:286527]"}, {"versioned_ensembl_gene_id":"ENSG00000101812.12","gene_symbol":"H2BFM","gene_name":"H2B histone family member M [Source:HGNC Symbol;Acc:HGNC:27867]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286436","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the H2B histone family. [provided by RefSeq, Nov 2015]","start":104039949,"end":104042454,"strand":1,"description":"H2B histone family member M [Source:HGNC Symbol;Acc:HGNC:27867]"}, {"versioned_ensembl_gene_id":"ENSG00000256218.1","gene_symbol":"AC007848.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5366048,"end":5367774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256146.1","gene_symbol":"AC006206.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5315961,"end":5319347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000046647.13","gene_symbol":"GEMIN8","gene_name":"gem nuclear organelle associated protein 8 [Source:HGNC Symbol;Acc:HGNC:26044]","synonyms":"FLJ20514,FAM51A1","biotype":"protein_coding","ncbi_id":"54960","summary":"The protein encoded by this gene is part of the SMN complex, which is necessary for spliceosomal snRNP assembly in the cytoplasm and pre-mRNA splicing in the nucleus. The encoded protein binds to both SMN1 and the GEMIN6/GEMIN7 heterodimer, mediating their interaction. This protein is found in nuclear Gemini of Cajal bodies (gems) and in the cytoplasm. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]","start":14008279,"end":14029893,"strand":-1,"description":"gem nuclear organelle associated protein 8 [Source:HGNC Symbol;Acc:HGNC:26044]"}, {"versioned_ensembl_gene_id":"ENSG00000212182.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":114005440,"end":114005655,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000107104.18","gene_symbol":"KANK1","gene_name":"KN motif and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:19309]","synonyms":"KIAA0172,KANK,ANKRD15","biotype":"protein_coding","ncbi_id":"23189","summary":"The protein encoded by this gene belongs to the Kank family of proteins, which contain multiple ankyrin repeat domains. This family member functions in cytoskeleton formation by regulating actin polymerization. This gene is a candidate tumor suppressor for renal cell carcinoma. Mutations in this gene cause cerebral palsy spastic quadriplegic type 2, a central nervous system development disorder. A t(5;9) translocation results in fusion of the platelet-derived growth factor receptor beta gene (PDGFRB) on chromosome 5 with this gene in a myeloproliferative neoplasm featuring severe thrombocythemia. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 20. [provided by RefSeq, Dec 2014]","start":470291,"end":746106,"strand":1,"description":"KN motif and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:HGNC:19309]"}, {"versioned_ensembl_gene_id":"ENSG00000232752.1","gene_symbol":"MTCO3P21","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52083]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075162","summary":null,"start":93924743,"end":93925385,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52083]"}, {"versioned_ensembl_gene_id":"ENSG00000267560.1","gene_symbol":"AC027514.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62300036,"end":62300998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227155.7","gene_symbol":"AL161725.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":452492,"end":492248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256115.5","gene_symbol":"LINC02443","gene_name":"long intergenic non-protein coding RNA 2443 [Source:HGNC Symbol;Acc:HGNC:53375]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929584","summary":null,"start":5233997,"end":5243151,"strand":-1,"description":"long intergenic non-protein coding RNA 2443 [Source:HGNC Symbol;Acc:HGNC:53375]"}, {"versioned_ensembl_gene_id":"ENSG00000235880.1","gene_symbol":"AL158832.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":267966,"end":273002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132423.11","gene_symbol":"COQ3","gene_name":"coenzyme Q3, methyltransferase [Source:HGNC Symbol;Acc:HGNC:18175]","synonyms":"bA9819.1","biotype":"protein_coding","ncbi_id":"51805","summary":"Ubiquinone, also known as coenzyme Q, or Q, is a critical component of the electron transport pathways of both eukaryotes and prokaryotes (Jonassen and Clarke, 2000 [PubMed 10777520]). This lipid consists of a hydrophobic isoprenoid tail and a quinone head group. The tail varies in length depending on the organism, but its purpose is to anchor coenzyme Q to the membrane. The quinone head group is responsible for the activity of coenzyme Q in the respiratory chain. The S. cerevisiae COQ3 gene encodes an O-methyltransferase required for 2 steps in the biosynthetic pathway of coenzyme Q. This enzyme methylates an early coenzyme Q intermediate, 3,4-dihydroxy-5-polyprenylbenzoic acid, as well as the final intermediate in the pathway, converting demethyl-ubiquinone to coenzyme Q. The COQ3 gene product is also capable of methylating the distinct prokaryotic early intermediate 2-hydroxy-6-polyprenyl phenol.[supplied by OMIM, Mar 2008]","start":99369400,"end":99394204,"strand":-1,"description":"coenzyme Q3, methyltransferase [Source:HGNC Symbol;Acc:HGNC:18175]"}, {"versioned_ensembl_gene_id":"ENSG00000228115.1","gene_symbol":"AL161725.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":487774,"end":495610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196420.7","gene_symbol":"S100A5","gene_name":"S100 calcium binding protein A5 [Source:HGNC Symbol;Acc:HGNC:10495]","synonyms":"S100D","biotype":"protein_coding","ncbi_id":"6276","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein has a Ca2+ affinity 20- to 100-fold higher than the other S100 proteins studied under identical conditions. This protein also binds Zn2+ and Cu2+, and Cu2+ strongly which impairs the binding of Ca2+. This protein is expressed in very restricted regions of the adult brain. [provided by RefSeq, Jul 2008]","start":153537147,"end":153541765,"strand":-1,"description":"S100 calcium binding protein A5 [Source:HGNC Symbol;Acc:HGNC:10495]"}, {"versioned_ensembl_gene_id":"ENSG00000214465.3","gene_symbol":"SMARCE1P6","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39737]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646196","summary":null,"start":26149204,"end":26150731,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39737]"}, {"versioned_ensembl_gene_id":"ENSG00000231655.1","gene_symbol":"AC011742.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26140263,"end":26141264,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253986.1","gene_symbol":"AC104561.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23493009,"end":23494198,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146267.11","gene_symbol":"FAXC","gene_name":"failed axon connections homolog [Source:HGNC Symbol;Acc:HGNC:20742]","synonyms":"MGC2817,dJ273F20,C6orf168","biotype":"protein_coding","ncbi_id":"84553","summary":null,"start":99271169,"end":99350062,"strand":-1,"description":"failed axon connections homolog [Source:HGNC Symbol;Acc:HGNC:20742]"}, {"versioned_ensembl_gene_id":"ENSG00000010438.16","gene_symbol":"PRSS3","gene_name":"protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:9486]","synonyms":"TRY4,TRY3,PRSS4","biotype":"protein_coding","ncbi_id":"5646","summary":"This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is expressed in the brain and pancreas and is resistant to common trypsin inhibitors. It is active on peptide linkages involving the carboxyl group of lysine or arginine. This gene is localized to the locus of T cell receptor beta variable orphans on chromosome 9. Four transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2010]","start":33750466,"end":33799231,"strand":1,"description":"protease, serine 3 [Source:HGNC Symbol;Acc:HGNC:9486]"}, {"versioned_ensembl_gene_id":"ENSG00000234380.1","gene_symbol":"LINC01426","gene_name":"long intergenic non-protein coding RNA 1426 [Source:HGNC Symbol;Acc:HGNC:50734]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506385","summary":null,"start":34745757,"end":34784886,"strand":1,"description":"long intergenic non-protein coding RNA 1426 [Source:HGNC Symbol;Acc:HGNC:50734]"}, {"versioned_ensembl_gene_id":"ENSG00000271142.1","gene_symbol":"YWHAQP7","gene_name":"YWHAQ pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422674","summary":null,"start":76619386,"end":76620043,"strand":1,"description":"YWHAQ pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37686]"}, {"versioned_ensembl_gene_id":"ENSG00000214286.2","gene_symbol":"PDCL3P3","gene_name":"phosducin-like 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44504]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132683","summary":null,"start":17877455,"end":17878169,"strand":-1,"description":"phosducin-like 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44504]"}, {"versioned_ensembl_gene_id":"ENSG00000282703.1","gene_symbol":"GLIS2-AS1","gene_name":"GLIS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51381]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926896","summary":null,"start":4324667,"end":4328340,"strand":-1,"description":"GLIS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51381]"}, {"versioned_ensembl_gene_id":"ENSG00000270087.5","gene_symbol":"AC010997.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75279726,"end":75401246,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169062.14","gene_symbol":"UPF3A","gene_name":"UPF3A, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:20332]","synonyms":"UPF3,RENT3A,HUPF3A","biotype":"protein_coding","ncbi_id":"65110","summary":"This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. The encoded protein is one of two functional homologs to yeast Upf3p. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein binds to the mRNA and remains bound after nuclear export, acting as a nucleocytoplasmic shuttling protein. It forms with Y14 a complex that binds specifically 20 nt upstream of exon-exon junctions. This gene is located on the long arm of chromosome 13. Several splice variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":114281584,"end":114305817,"strand":1,"description":"UPF3A, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:20332]"}, {"versioned_ensembl_gene_id":"ENSG00000022277.12","gene_symbol":"RTFDC1","gene_name":"replication termination factor 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15890]","synonyms":"HSPC164,CDAO5,C20orf43","biotype":"protein_coding","ncbi_id":"51507","summary":null,"start":56468585,"end":56519449,"strand":1,"description":"replication termination factor 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:15890]"}, {"versioned_ensembl_gene_id":"ENSG00000241685.9","gene_symbol":"ARPC1A","gene_name":"actin related protein 2/3 complex subunit 1A [Source:HGNC Symbol;Acc:HGNC:703]","synonyms":"SOP2L,SOP2Hs,Arc40","biotype":"protein_coding","ncbi_id":"10552","summary":"This gene encodes one of seven subunits of the human Arp2/3 protein complex. This subunit is a member of the SOP2 family of proteins and is most similar to the protein encoded by gene ARPC1B. The similarity between these two proteins suggests that they both may function as p41 subunit of the human Arp2/3 complex that has been implicated in the control of actin polymerization in cells. It is possible that the p41 subunit is involved in assembling and maintaining the structure of the Arp2/3 complex. Multiple versions of the p41 subunit may adapt the functions of the complex to different cell types or developmental stages. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":99325910,"end":99366262,"strand":1,"description":"actin related protein 2/3 complex subunit 1A [Source:HGNC Symbol;Acc:HGNC:703]"}, {"versioned_ensembl_gene_id":"ENSG00000273155.1","gene_symbol":"AC092587.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99154998,"end":99195298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284292.1","gene_symbol":"AC004922.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99325879,"end":99394653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076984.17","gene_symbol":"MAP2K7","gene_name":"mitogen-activated protein kinase kinase 7 [Source:HGNC Symbol;Acc:HGNC:6847]","synonyms":"PRKMK7,MKK7,Jnkk2","biotype":"protein_coding","ncbi_id":"5609","summary":"The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase specifically activates MAPK8/JNK1 and MAPK9/JNK2, and this kinase itself is phosphorylated and activated by MAP kinase kinase kinases including MAP3K1/MEKK1, MAP3K2/MEKK2,MAP3K3/MEKK5, and MAP4K2/GCK. This kinase is involved in the signal transduction mediating the cell responses to proinflammatory cytokines, and environmental stresses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":7903843,"end":7914478,"strand":1,"description":"mitogen-activated protein kinase kinase 7 [Source:HGNC Symbol;Acc:HGNC:6847]"}, {"versioned_ensembl_gene_id":"ENSG00000251248.1","gene_symbol":"AC139720.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":142514446,"end":142518983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197956.9","gene_symbol":"S100A6","gene_name":"S100 calcium binding protein A6 [Source:HGNC Symbol;Acc:HGNC:10496]","synonyms":"CABP,2A9,PRA,CACY","biotype":"protein_coding","ncbi_id":"6277","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in stimulation of Ca2+-dependent insulin release, stimulation of prolactin secretion, and exocytosis. Chromosomal rearrangements and altered expression of this gene have been implicated in melanoma. [provided by RefSeq, Jul 2008]","start":153534599,"end":153536244,"strand":-1,"description":"S100 calcium binding protein A6 [Source:HGNC Symbol;Acc:HGNC:10496]"}, {"versioned_ensembl_gene_id":"ENSG00000219095.1","gene_symbol":"DHFRP6","gene_name":"dihydrofolate reductase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52356]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729123","summary":null,"start":56276529,"end":56276796,"strand":-1,"description":"dihydrofolate reductase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:52356]"}, {"versioned_ensembl_gene_id":"ENSG00000273413.1","gene_symbol":"AL136982.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86970237,"end":86970826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271880.1","gene_symbol":"AGAP11","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 11 [Source:HGNC Symbol;Acc:HGNC:29421]","synonyms":"KIAA1975","biotype":"processed_transcript","ncbi_id":"119385","summary":null,"start":86970741,"end":87010126,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 11 [Source:HGNC Symbol;Acc:HGNC:29421]"}, {"versioned_ensembl_gene_id":"ENSG00000235039.1","gene_symbol":"MTND6P12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39475]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481743","summary":null,"start":5168918,"end":5169439,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39475]"}, {"versioned_ensembl_gene_id":"ENSG00000232845.1","gene_symbol":"TRAPPC2P9","gene_name":"trafficking protein particle complex 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37733]","synonyms":"TRAPPC2P4B","biotype":"unprocessed_pseudogene","ncbi_id":"414753","summary":null,"start":23762838,"end":23765583,"strand":-1,"description":"trafficking protein particle complex 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37733]"}, {"versioned_ensembl_gene_id":"ENSG00000235549.1","gene_symbol":"EIF1P2","gene_name":"eukaryotic translation initiation factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288425","summary":null,"start":38958275,"end":38958925,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49615]"}, {"versioned_ensembl_gene_id":"ENSG00000276286.4","gene_symbol":"ADAM2","gene_name":"ADAM metallopeptidase domain 2 [Source:HGNC Symbol;Acc:HGNC:198]","synonyms":"PH30,PH-30b,FTNB,CT15","biotype":"protein_coding","ncbi_id":"2515","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded protein is a subunit of an integral sperm membrane glycoprotein called fertilin, which plays an important role in sperm-egg interactions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":39588691,"end":39683242,"strand":-1,"description":"ADAM metallopeptidase domain 2 [Source:HGNC Symbol;Acc:HGNC:198]"}, {"versioned_ensembl_gene_id":"ENSG00000171017.10","gene_symbol":"LRRC8E","gene_name":"leucine rich repeat containing 8 family member E [Source:HGNC Symbol;Acc:HGNC:26272]","synonyms":"FLJ23420","biotype":"protein_coding","ncbi_id":"80131","summary":"This gene encodes a member of a small, conserved family of proteins with similar structure, including a string of extracellular leucine-rich repeats. A related protein was shown to be involved in B-cell development. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012]","start":7888505,"end":7902021,"strand":1,"description":"leucine rich repeat containing 8 family member E [Source:HGNC Symbol;Acc:HGNC:26272]"}, {"versioned_ensembl_gene_id":"ENSG00000214248.2","gene_symbol":"AC010336.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7898804,"end":7903542,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244491.1","gene_symbol":"AL021707.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38734725,"end":38738765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235024.1","gene_symbol":"AC097468.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":218944629,"end":218961903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267478.1","gene_symbol":"AP002414.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12091674,"end":12093141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183248.11","gene_symbol":"PRR36","gene_name":"proline rich 36 [Source:HGNC Symbol;Acc:HGNC:26172]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80164","summary":"This gene encodes a large protein of unknown function that contains internal regions of low complexity sequence. Alternative splicing results in multiple transcript variants. The transcript structure of the protein-coding variant at this locus is conserved between human and mouse. [provided by RefSeq, Oct 2013]","start":7868719,"end":7874379,"strand":-1,"description":"proline rich 36 [Source:HGNC Symbol;Acc:HGNC:26172]"}, {"versioned_ensembl_gene_id":"ENSG00000236349.1","gene_symbol":"SUCLG2P2","gene_name":"succinate-CoA ligase GDP-forming beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43997]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283398","summary":null,"start":94548241,"end":94549536,"strand":1,"description":"succinate-CoA ligase GDP-forming beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43997]"}, {"versioned_ensembl_gene_id":"ENSG00000283025.1","gene_symbol":"AC027045.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9805443,"end":9811047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205663.5","gene_symbol":"FAM239B","gene_name":"family with sequence similarity 239 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53415]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3891438,"end":3920746,"strand":-1,"description":"family with sequence similarity 239 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53415]"}, {"versioned_ensembl_gene_id":"ENSG00000270149.5","gene_symbol":"AL591806.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":160997957,"end":161038962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232341.2","gene_symbol":"RPL4P2","gene_name":"ribosomal protein L4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36836]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646688","summary":null,"start":166747379,"end":166748660,"strand":1,"description":"ribosomal protein L4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36836]"}, {"versioned_ensembl_gene_id":"ENSG00000123066.7","gene_symbol":"MED13L","gene_name":"mediator complex subunit 13 like [Source:HGNC Symbol;Acc:HGNC:22962]","synonyms":"TRAP240L,THRAP2,KIAA1025","biotype":"protein_coding","ncbi_id":"23389","summary":"The protein encoded by this gene is a subunit of the Mediator complex, a large complex of proteins that functions as a transcriptional coactivator for most RNA polymerase II-transcribed genes. The encoded protein is involved in early development of the heart and brain. Defects in this gene are a cause of transposition of the great arteries, dextro-looped (DTGA).[provided by RefSeq, Jul 2010]","start":115953872,"end":116277338,"strand":-1,"description":"mediator complex subunit 13 like [Source:HGNC Symbol;Acc:HGNC:22962]"}, {"versioned_ensembl_gene_id":"ENSG00000182187.3","gene_symbol":"CRYGB","gene_name":"crystallin gamma B [Source:HGNC Symbol;Acc:HGNC:2409]","synonyms":"CRYG2","biotype":"protein_coding","ncbi_id":"1419","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. Four gamma-crystallin genes (gamma-A through gamma-D) and three pseudogenes (gamma-E, gamma-F, gamma-G) are tandemly organized in a genomic segment as a gene cluster. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation. [provided by RefSeq, Jul 2008]","start":208142573,"end":208146168,"strand":-1,"description":"crystallin gamma B [Source:HGNC Symbol;Acc:HGNC:2409]"}, {"versioned_ensembl_gene_id":"ENSG00000117228.9","gene_symbol":"GBP1","gene_name":"guanylate binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4182]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2633","summary":"Guanylate binding protein expression is induced by interferon. Guanylate binding proteins are characterized by their ability to specifically bind guanine nucleotides (GMP, GDP, and GTP) and are distinguished from the GTP-binding proteins by the presence of 2 binding motifs rather than 3. [provided by RefSeq, Jul 2008]","start":89052319,"end":89065360,"strand":-1,"description":"guanylate binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4182]"}, {"versioned_ensembl_gene_id":"ENSG00000224529.1","gene_symbol":"AC093698.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208135394,"end":208137697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197905.8","gene_symbol":"TEAD4","gene_name":"TEA domain transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:11717]","synonyms":"TEF-3,TCF13L1,RTEF-1,EFTR-2,TEFR-1","biotype":"protein_coding","ncbi_id":"7004","summary":"This gene product is a member of the transcriptional enhancer factor (TEF) family of transcription factors, which contain the TEA/ATTS DNA-binding domain. It is preferentially expressed in the skeletal muscle, and binds to the M-CAT regulatory element found in promoters of muscle-specific genes to direct their gene expression. Alternatively spliced transcripts encoding distinct isoforms, some of which are translated through the use of a non-AUG (UUG) initiation codon, have been described for this gene. [provided by RefSeq, Jul 2008]","start":2959330,"end":3040673,"strand":1,"description":"TEA domain transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:11717]"}, {"versioned_ensembl_gene_id":"ENSG00000173976.15","gene_symbol":"RAX2","gene_name":"retina and anterior neural fold homeobox 2 [Source:HGNC Symbol;Acc:HGNC:18286]","synonyms":"RAXL1,MGC15631,CORD11,ARMD6","biotype":"protein_coding","ncbi_id":"84839","summary":"This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":3769089,"end":3772221,"strand":-1,"description":"retina and anterior neural fold homeobox 2 [Source:HGNC Symbol;Acc:HGNC:18286]"}, {"versioned_ensembl_gene_id":"ENSG00000226595.1","gene_symbol":"AC245291.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22465659,"end":22465986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228045.1","gene_symbol":"DNAJA1P6","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39342]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421542","summary":null,"start":17518676,"end":17519029,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39342]"}, {"versioned_ensembl_gene_id":"ENSG00000261971.6","gene_symbol":"MMP25-AS1","gene_name":"MMP25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51372]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507419","summary":null,"start":3051096,"end":3059370,"strand":-1,"description":"MMP25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51372]"}, {"versioned_ensembl_gene_id":"ENSG00000184402.14","gene_symbol":"SS18L1","gene_name":"SS18L1, nBAF chromatin remodeling complex subunit [Source:HGNC Symbol;Acc:HGNC:15592]","synonyms":"KIAA0693,CREST","biotype":"protein_coding","ncbi_id":"26039","summary":"This gene encodes a calcium-responsive transactivator which is an essential subunit of a neuron-specific chromatin-remodeling complex. The structure of this gene is similar to that of the SS18 gene. Mutations in this gene are involved in amyotrophic lateral sclerosis (ALS). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":62143795,"end":62182484,"strand":1,"description":"SS18L1, nBAF chromatin remodeling complex subunit [Source:HGNC Symbol;Acc:HGNC:15592]"}, {"versioned_ensembl_gene_id":"ENSG00000230821.1","gene_symbol":"AC245291.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22446686,"end":22448336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211654.2","gene_symbol":"IGLV5-37","gene_name":"immunoglobulin lambda variable 5-37 [Source:HGNC Symbol;Acc:HGNC:5922]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28783","summary":null,"start":22427540,"end":22428035,"strand":1,"description":"immunoglobulin lambda variable 5-37 [Source:HGNC Symbol;Acc:HGNC:5922]"}, {"versioned_ensembl_gene_id":"ENSG00000267292.1","gene_symbol":"AP001542.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12050309,"end":12050672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258136.1","gene_symbol":"AC007622.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107736555,"end":107759968,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241991.1","gene_symbol":"AC114982.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62561859,"end":62562216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258092.1","gene_symbol":"AC005841.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2797136,"end":2803938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283587.1","gene_symbol":"AC092471.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2726400,"end":2727050,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158427.14","gene_symbol":"TMSB15B","gene_name":"thymosin beta 15B [Source:HGNC Symbol;Acc:HGNC:28612]","synonyms":"MGC39900,Tbeta15b","biotype":"protein_coding","ncbi_id":"286527","summary":null,"start":103918896,"end":103966712,"strand":1,"description":"thymosin beta 15B [Source:HGNC Symbol;Acc:HGNC:28612]"}, {"versioned_ensembl_gene_id":"ENSG00000230312.2","gene_symbol":"AC234782.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103928099,"end":103929017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236407.1","gene_symbol":"HMGB1P18","gene_name":"high mobility group box 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39100]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646526","summary":null,"start":80283352,"end":80283970,"strand":1,"description":"high mobility group box 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39100]"}, {"versioned_ensembl_gene_id":"ENSG00000244159.1","gene_symbol":"RPS27AP13","gene_name":"ribosomal protein S27a pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36667]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130300","summary":null,"start":53887008,"end":53887244,"strand":-1,"description":"ribosomal protein S27a pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36667]"}, {"versioned_ensembl_gene_id":"ENSG00000260598.1","gene_symbol":"FRG2IP","gene_name":"FSHD region gene 2 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:51795]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480351","summary":null,"start":35405747,"end":35407349,"strand":-1,"description":"FSHD region gene 2 family member I, pseudogene [Source:HGNC Symbol;Acc:HGNC:51795]"}, {"versioned_ensembl_gene_id":"ENSG00000197815.4","gene_symbol":"AC122129.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17858227,"end":17860041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281683.1","gene_symbol":"AP001803.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56747390,"end":56747536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233517.1","gene_symbol":"AC005162.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28987028,"end":28988899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013725.14","gene_symbol":"CD6","gene_name":"CD6 molecule [Source:HGNC Symbol;Acc:HGNC:1691]","synonyms":"Tp120","biotype":"protein_coding","ncbi_id":"923","summary":"This gene encodes a protein found on the outer membrane of T-lymphocytes as well as some other immune cells. The encoded protein contains three scavenger receptor cysteine-rich (SRCR) domains and a binding site for an activated leukocyte cell adhesion molecule. The gene product is important for continuation of T cell activation. This gene may be associated with susceptibility to multiple sclerosis (PMID: 19525953, 21849685). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":60971680,"end":61020377,"strand":1,"description":"CD6 molecule [Source:HGNC Symbol;Acc:HGNC:1691]"}, {"versioned_ensembl_gene_id":"ENSG00000274114.2","gene_symbol":"AC004706.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6657034,"end":6693577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111203.11","gene_symbol":"ITFG2","gene_name":"integrin alpha FG-GAP repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:30879]","synonyms":"MDS028,FGGAP1","biotype":"protein_coding","ncbi_id":"55846","summary":null,"start":2812622,"end":2859791,"strand":1,"description":"integrin alpha FG-GAP repeat containing 2 [Source:HGNC Symbol;Acc:HGNC:30879]"}, {"versioned_ensembl_gene_id":"ENSG00000261996.1","gene_symbol":"AC004706.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6653464,"end":6655009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167996.15","gene_symbol":"FTH1","gene_name":"ferritin heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:3976]","synonyms":"PLIF,PIG15,FTHL6,FTH,FHC","biotype":"protein_coding","ncbi_id":"2495","summary":"This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":61959718,"end":61967660,"strand":-1,"description":"ferritin heavy chain 1 [Source:HGNC Symbol;Acc:HGNC:3976]"}, {"versioned_ensembl_gene_id":"ENSG00000226757.2","gene_symbol":"PP12613","gene_name":"uncharacterized LOC100192379 [Source:NCBI gene;Acc:100192379]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100192379","summary":null,"start":121764585,"end":121766814,"strand":1,"description":"uncharacterized LOC100192379 [Source:NCBI gene;Acc:100192379]"}, {"versioned_ensembl_gene_id":"ENSG00000244151.1","gene_symbol":"AC010973.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151074742,"end":151076530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260963.1","gene_symbol":"AC026462.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52607349,"end":52613908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233573.9","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30093221,"end":30103423,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000232510.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30095564,"end":30105041,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000277670.1","gene_symbol":"AC098657.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80124004,"end":80124361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261261.2","gene_symbol":"AC026462.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52622115,"end":52631088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260393.1","gene_symbol":"AC026462.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52607762,"end":52608158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257781.1","gene_symbol":"AC009387.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115755262,"end":115799936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151065.13","gene_symbol":"DCP1B","gene_name":"decapping mRNA 1B [Source:HGNC Symbol;Acc:HGNC:24451]","synonyms":"FLJ31638","biotype":"protein_coding","ncbi_id":"196513","summary":"This gene encodes a member of a family of proteins that function in removing the 5' cap from mRNAs, which is a step in regulated mRNA decay. This protein localizes to cytoplasmic foci which are the site of mRNA breakdown and turnover. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":1946054,"end":2004535,"strand":-1,"description":"decapping mRNA 1B [Source:HGNC Symbol;Acc:HGNC:24451]"}, {"versioned_ensembl_gene_id":"ENSG00000237274.2","gene_symbol":"GTF3AP1","gene_name":"general transcription factor IIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49744]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100135064","summary":null,"start":6195934,"end":6197248,"strand":1,"description":"general transcription factor IIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49744]"}, {"versioned_ensembl_gene_id":"ENSG00000123570.3","gene_symbol":"RAB9B","gene_name":"RAB9B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14090]","synonyms":"RAB9L","biotype":"protein_coding","ncbi_id":"51209","summary":"This gene encodes a member of a subfamily of RAS small guanosine triphosphate (GTP)-binding proteins that regulate membrane trafficking. The encoded protein may be involved in endosome-to-Golgi transport. [provided by RefSeq, Jan 2010]","start":103822322,"end":103832228,"strand":-1,"description":"RAB9B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14090]"}, {"versioned_ensembl_gene_id":"ENSG00000257407.1","gene_symbol":"AC009803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115582061,"end":115639734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259431.5","gene_symbol":"THTPA","gene_name":"thiamine triphosphatase [Source:HGNC Symbol;Acc:HGNC:18987]","synonyms":"THTPASE","biotype":"protein_coding","ncbi_id":"79178","summary":"This gene encodes an enzyme which catalyzes the biosynthesis of thiamine disphophate (vitamin B1) by hydrolysis of thiamine triphosphate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]","start":23555988,"end":23560271,"strand":1,"description":"thiamine triphosphatase [Source:HGNC Symbol;Acc:HGNC:18987]"}, {"versioned_ensembl_gene_id":"ENSG00000235440.1","gene_symbol":"AC011742.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26101317,"end":26102136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271459.1","gene_symbol":"Z98751.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171755803,"end":171756323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232261.1","gene_symbol":"Z98751.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":171751543,"end":171752025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008516.16","gene_symbol":"MMP25","gene_name":"matrix metallopeptidase 25 [Source:HGNC Symbol;Acc:HGNC:14246]","synonyms":"MT6-MMP,MMPL1,MMP20","biotype":"protein_coding","ncbi_id":"64386","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMPs are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily, attached to the plasma membrane via a glycosylphosphatidyl inositol anchor. In response to bacterial infection or inflammation, the encoded protein is thought to inactivate alpha-1 proteinase inhibitor, a major tissue protectant against proteolytic enzymes released by activated neutrophils, facilitating the transendothelial migration of neutrophils to inflammatory sites. The encoded protein may also play a role in tumor invasion and metastasis through activation of MMP2. The gene has previously been referred to as MMP20 but has been renamed MMP25. [provided by RefSeq, Jul 2008]","start":3046681,"end":3060726,"strand":1,"description":"matrix metallopeptidase 25 [Source:HGNC Symbol;Acc:HGNC:14246]"}, {"versioned_ensembl_gene_id":"ENSG00000259869.1","gene_symbol":"AL022344.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42751178,"end":42752145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278356.1","gene_symbol":"AC005911.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2885819,"end":2886329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126705.13","gene_symbol":"AHDC1","gene_name":"AT-hook DNA binding motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25230]","synonyms":"RP1-159A19.1,DJ159A19.3","biotype":"protein_coding","ncbi_id":"27245","summary":"This gene encodes a protein containing two AT-hooks, which likely function in DNA binding. Mutations in this gene were found in individuals with Xia-Gibbs syndrome. [provided by RefSeq, Jun 2014]","start":27534035,"end":27604431,"strand":-1,"description":"AT-hook DNA binding motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25230]"}, {"versioned_ensembl_gene_id":"ENSG00000251309.1","gene_symbol":"AP002075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101976894,"end":102036903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186105.7","gene_symbol":"LRRC70","gene_name":"leucine rich repeat containing 70 [Source:HGNC Symbol;Acc:HGNC:35155]","synonyms":"SLRN,LOC100130733","biotype":"protein_coding","ncbi_id":"100130733","summary":null,"start":62578735,"end":62581448,"strand":1,"description":"leucine rich repeat containing 70 [Source:HGNC Symbol;Acc:HGNC:35155]"}, {"versioned_ensembl_gene_id":"ENSG00000235132.8","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H8,OR2H6,OR6-2","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29453753,"end":29460899,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000258280.1","gene_symbol":"AC009803.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115576676,"end":115577615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229982.1","gene_symbol":"GTF3AP6","gene_name":"general transcription factor IIIA pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49749]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100135063","summary":null,"start":118880103,"end":118881288,"strand":-1,"description":"general transcription factor IIIA pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49749]"}, {"versioned_ensembl_gene_id":"ENSG00000231747.1","gene_symbol":"AC079922.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112621809,"end":112622167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244932.2","gene_symbol":"AL449212.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":129381298,"end":129394149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276308.1","gene_symbol":"AC078880.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115318657,"end":115320405,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274177.1","gene_symbol":"AC004528.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1010221,"end":1010907,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124374.8","gene_symbol":"PAIP2B","gene_name":"poly(A) binding protein interacting protein 2B [Source:HGNC Symbol;Acc:HGNC:29200]","synonyms":"KIAA1155","biotype":"protein_coding","ncbi_id":"400961","summary":"Most mRNAs, except for histones, contain a 3-prime poly(A) tail. Poly(A)-binding protein (PABP; see MIM 604679) enhances translation by circularizing mRNA through its interaction with the translation initiation factor EIF4G1 (MIM 600495) and the poly(A) tail. Various PABP-binding proteins regulate PABP activity, including PAIP1 (MIM 605184), a translational stimulator, and PAIP2A (MIM 605604) and PAIP2B, translational inhibitors (Derry et al., 2006 [PubMed 17381337]).[supplied by OMIM, Mar 2008]","start":71182739,"end":71227083,"strand":-1,"description":"poly(A) binding protein interacting protein 2B [Source:HGNC Symbol;Acc:HGNC:29200]"}, {"versioned_ensembl_gene_id":"ENSG00000273167.1","gene_symbol":"AL359736.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23979700,"end":24321031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251474.6","gene_symbol":"RPL32P3","gene_name":"ribosomal protein L32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27024]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"132241","summary":null,"start":129382922,"end":129399655,"strand":-1,"description":"ribosomal protein L32 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27024]"}, {"versioned_ensembl_gene_id":"ENSG00000233515.1","gene_symbol":"LINC01518","gene_name":"long intergenic non-protein coding RNA 1518 [Source:HGNC Symbol;Acc:HGNC:51216]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929397","summary":null,"start":42674197,"end":42691723,"strand":-1,"description":"long intergenic non-protein coding RNA 1518 [Source:HGNC Symbol;Acc:HGNC:51216]"}, {"versioned_ensembl_gene_id":"ENSG00000036448.9","gene_symbol":"MYOM2","gene_name":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9172","summary":"The giant protein titin, together with its associated proteins, interconnects the major structure of sarcomeres, the M bands and Z discs. The C-terminal end of the titin string extends into the M line, where it binds tightly to M-band constituents of apparent molecular masses of 190 kD and 165 kD. The predicted MYOM2 protein contains 1,465 amino acids. Like MYOM1, MYOM2 has a unique N-terminal domain followed by 12 repeat domains with strong homology to either fibronectin type III or immunoglobulin C2 domains. Protein sequence comparisons suggested that the MYOM2 protein and bovine M protein are identical. [provided by RefSeq, Jul 2008]","start":2045040,"end":2165552,"strand":1,"description":"myomesin 2 [Source:HGNC Symbol;Acc:HGNC:7614]"}, {"versioned_ensembl_gene_id":"ENSG00000229048.5","gene_symbol":"DUTP1","gene_name":"deoxyuridine triphosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31956]","synonyms":"DUTL","biotype":"processed_pseudogene","ncbi_id":"548637","summary":null,"start":125310881,"end":125311350,"strand":1,"description":"deoxyuridine triphosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31956]"}, {"versioned_ensembl_gene_id":"ENSG00000243389.1","gene_symbol":"AC012442.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":112589040,"end":112614431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158270.11","gene_symbol":"COLEC12","gene_name":"collectin subfamily member 12 [Source:HGNC Symbol;Acc:HGNC:16016]","synonyms":"SRCL,SCARA4,CL-P1","biotype":"protein_coding","ncbi_id":"81035","summary":"This gene encodes a member of the C-lectin family, proteins that possess collagen-like sequences and carbohydrate recognition domains. This protein is a scavenger receptor that displays several functions associated with host defense. It can bind to carbohydrate antigens on microorganisms, facilitating their recognition and removal. It also mediates the recognition, internalization, and degradation of oxidatively modified low density lipoprotein by vascular endothelial cells. [provided by RefSeq, May 2018]","start":316740,"end":500722,"strand":-1,"description":"collectin subfamily member 12 [Source:HGNC Symbol;Acc:HGNC:16016]"}, {"versioned_ensembl_gene_id":"ENSG00000259500.1","gene_symbol":"KRT8P24","gene_name":"keratin 8 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:33376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729344","summary":null,"start":48971803,"end":48973361,"strand":1,"description":"keratin 8 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:33376]"}, {"versioned_ensembl_gene_id":"ENSG00000250011.1","gene_symbol":"HMGB1P3","gene_name":"high mobility group box 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4995]","synonyms":"HMGB1L3,HMG1L3","biotype":"processed_pseudogene","ncbi_id":"10356","summary":null,"start":230515023,"end":230515638,"strand":1,"description":"high mobility group box 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:4995]"}, {"versioned_ensembl_gene_id":"ENSG00000002079.14","gene_symbol":"MYH16","gene_name":"myosin heavy chain 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:31038]","synonyms":"MYH5,MYH16P,MHC20","biotype":"transcribed_unitary_pseudogene","ncbi_id":"84176","summary":"The MYH16 gene, encoding a sarcomeric myosin heavy chain expressed in nonhuman primate masticatory muscles, is inactivated in humans. Stedman et al. (2004) [PubMed 15042088] hypothesized that the decrement in masticatory muscle size caused by the inactivation of MYH16 removed an evolutionary constraint on encephalization in early man.[supplied by OMIM, Mar 2008]","start":99238829,"end":99311130,"strand":1,"description":"myosin heavy chain 16 pseudogene [Source:HGNC Symbol;Acc:HGNC:31038]"}, {"versioned_ensembl_gene_id":"ENSG00000273893.1","gene_symbol":"AL133520.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46681676,"end":46682375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223764.2","gene_symbol":"AL645608.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":916865,"end":921016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283040.1","gene_symbol":"AL669831.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":874529,"end":877234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187763.3","gene_symbol":"OR2B7P","gene_name":"olfactory receptor family 2 subfamily B member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:13967]","synonyms":"hs6M1-31P","biotype":"unprocessed_pseudogene","ncbi_id":"81695","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":28046434,"end":28047367,"strand":1,"description":"olfactory receptor family 2 subfamily B member 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:13967]"}, {"versioned_ensembl_gene_id":"ENSG00000262201.2","gene_symbol":"LINC02403","gene_name":"long intergenic non-protein coding RNA 2403 [Source:HGNC Symbol;Acc:HGNC:53330]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"105369785","summary":null,"start":58097051,"end":58097709,"strand":1,"description":"long intergenic non-protein coding RNA 2403 [Source:HGNC Symbol;Acc:HGNC:53330]"}, {"versioned_ensembl_gene_id":"ENSG00000257488.5","gene_symbol":"LINC02354","gene_name":"long intergenic non-protein coding RNA 2354 [Source:HGNC Symbol;Acc:HGNC:53276]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984503","summary":null,"start":47826854,"end":47837898,"strand":1,"description":"long intergenic non-protein coding RNA 2354 [Source:HGNC Symbol;Acc:HGNC:53276]"}, {"versioned_ensembl_gene_id":"ENSG00000117226.11","gene_symbol":"GBP3","gene_name":"guanylate binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4184]","synonyms":"FLJ10961","biotype":"protein_coding","ncbi_id":"2635","summary":"This gene encodes a member of the guanylate-binding protein (GBP) family. GBPs specifically bind guanine nucleotides (GMP, GDP, and GTP) and contain two of the three consensus motifs found in typical GTP-binding proteins. The encoded protein interacts with a member of the germinal center kinase family. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2017]","start":89006666,"end":89022894,"strand":-1,"description":"guanylate binding protein 3 [Source:HGNC Symbol;Acc:HGNC:4184]"}, {"versioned_ensembl_gene_id":"ENSG00000229150.1","gene_symbol":"CRYGEP","gene_name":"crystallin gamma E, pseudogene [Source:HGNC Symbol;Acc:HGNC:2412]","synonyms":"CCL,G2,CRYGEP1,CRYG5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"200575","summary":null,"start":208108233,"end":208112511,"strand":-1,"description":"crystallin gamma E, pseudogene [Source:HGNC Symbol;Acc:HGNC:2412]"}, {"versioned_ensembl_gene_id":"ENSG00000270381.1","gene_symbol":"AL138963.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45263690,"end":45263915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224839.1","gene_symbol":"RPL12P17","gene_name":"ribosomal protein L12 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36263]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344471","summary":null,"start":208057248,"end":208057745,"strand":-1,"description":"ribosomal protein L12 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36263]"}, {"versioned_ensembl_gene_id":"ENSG00000230453.9","gene_symbol":"ANKRD18B","gene_name":"ankyrin repeat domain 18B [Source:HGNC Symbol;Acc:HGNC:23644]","synonyms":"bA255A11.3","biotype":"protein_coding","ncbi_id":"441459","summary":null,"start":33524394,"end":33573009,"strand":1,"description":"ankyrin repeat domain 18B [Source:HGNC Symbol;Acc:HGNC:23644]"}, {"versioned_ensembl_gene_id":"ENSG00000217539.2","gene_symbol":"IQCB2P","gene_name":"IQ motif containing B2 pseudogene [Source:HGNC Symbol;Acc:HGNC:17727]","synonyms":"IQCB1P1,dJ313I6.1","biotype":"processed_pseudogene","ncbi_id":"340192","summary":null,"start":28010723,"end":28012355,"strand":1,"description":"IQ motif containing B2 pseudogene [Source:HGNC Symbol;Acc:HGNC:17727]"}, {"versioned_ensembl_gene_id":"ENSG00000226002.1","gene_symbol":"GTF2IP14","gene_name":"general transcription factor IIi pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51726]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481735","summary":null,"start":65084103,"end":65100232,"strand":1,"description":"general transcription factor IIi pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51726]"}, {"versioned_ensembl_gene_id":"ENSG00000131149.18","gene_symbol":"GSE1","gene_name":"Gse1 coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:28979]","synonyms":"KIAA0182","biotype":"protein_coding","ncbi_id":"23199","summary":"This gene encodes a proline-rich protein with coiled coil domains that may be a subunit of a BRAF35-HDAC (BHC) histone deacetylase complex. This gene may function as an oncogene in breast cancer and enhanced expression of the encoded protein has been observed in breast cancer patients. [provided by RefSeq, May 2017]","start":85169525,"end":85676204,"strand":1,"description":"Gse1 coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:28979]"}, {"versioned_ensembl_gene_id":"ENSG00000256658.1","gene_symbol":"AC008115.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12723297,"end":12724011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272288.5","gene_symbol":"AL451165.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34696317,"end":34697470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000216636.1","gene_symbol":"RPL7P25","gene_name":"ribosomal protein L7 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36455]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129061","summary":null,"start":34616538,"end":34617258,"strand":1,"description":"ribosomal protein L7 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36455]"}, {"versioned_ensembl_gene_id":"ENSG00000277753.3","gene_symbol":"MUC20","gene_name":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]","synonyms":"KIAA1359,FLJ14408","biotype":"protein_coding","ncbi_id":"200958","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus of this family member associates with the multifunctional docking site of the MET proto-oncogene and suppresses activation of some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different isoforms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]","start":195719644,"end":195739354,"strand":1,"description":"mucin 20, cell surface associated [Source:HGNC Symbol;Acc:HGNC:23282]"}, {"versioned_ensembl_gene_id":"ENSG00000153975.9","gene_symbol":"ZUFSP","gene_name":"zinc finger with UFM1 specific peptidase domain [Source:HGNC Symbol;Acc:HGNC:21224]","synonyms":"dJ412I7.3,C6orf113","biotype":"protein_coding","ncbi_id":"221302","summary":"This gene encodes a protein containing zinc finger motifs and a cysteine peptidase domain. The encoded protein functions as a K63-specific de-ubiquitinating enzyme that specifically cleaves long K63-linked polyubiquitin chains in the middle of a chain (i.e. \"endo cleavage) rather than by removing the terminal ubiquitin from a chain. This enzyme is thought to be involved in the regulation of DNA repair by cleaving K63-linked ubiquitin chains at repair foci. This protein is related to proteases for the ubiquitin-like modifiers Ufm1 (ubiquitin fold modifier 1) and Atg8/Gabarapl2, but does not have any activity on these modifiers. [provided by RefSeq, Mar 2018]","start":116635618,"end":116668794,"strand":-1,"description":"zinc finger with UFM1 specific peptidase domain [Source:HGNC Symbol;Acc:HGNC:21224]"}, {"versioned_ensembl_gene_id":"ENSG00000248871.1","gene_symbol":"TNFSF12-TNFSF13","gene_name":"TNFSF12-TNFSF13 readthrough [Source:HGNC Symbol;Acc:HGNC:33537]","synonyms":"TWE-PRIL","biotype":"protein_coding","ncbi_id":"407977","summary":"This gene encodes a member of the tumor necrosis factor superfamily. It encodes a hybrid protein composed of the cytoplasmic and transmembrane domains of family member 12 fused to the C-terminal domain of family member 13. The hybrid protein is membrane anchored and presents the receptor-binding domain of family member 13 at the cell surface. It stimulates cycling in T- and B-lymphoma cell lines. [provided by RefSeq, Jul 2008]","start":7549099,"end":7561601,"strand":1,"description":"TNFSF12-TNFSF13 readthrough [Source:HGNC Symbol;Acc:HGNC:33537]"}, {"versioned_ensembl_gene_id":"ENSG00000196758.3","gene_symbol":"AC079612.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":239578301,"end":239586094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230398.1","gene_symbol":"HINT2P1","gene_name":"histidine triad nucleotide binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50311]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929471","summary":null,"start":2362258,"end":2362738,"strand":1,"description":"histidine triad nucleotide binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50311]"}, {"versioned_ensembl_gene_id":"ENSG00000220391.4","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"HCG4P6,HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3,bQB90C11.3","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29917179,"end":29918169,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000163666.8","gene_symbol":"HESX1","gene_name":"HESX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4877]","synonyms":"ANF,RPX","biotype":"protein_coding","ncbi_id":"8820","summary":"This gene encodes a conserved homeobox protein that is a transcriptional repressor in the developing forebrain and pituitary gland. Mutations in this gene are associated with septooptic dysplasia, HESX1-related growth hormone deficiency, and combined pituitary hormone deficiency. [provided by RefSeq, Jul 2008]","start":57197843,"end":57226521,"strand":-1,"description":"HESX homeobox 1 [Source:HGNC Symbol;Acc:HGNC:4877]"}, {"versioned_ensembl_gene_id":"ENSG00000224526.1","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29917655,"end":29920429,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000257056.2","gene_symbol":"LINC02282","gene_name":"long intergenic non-protein coding RNA 2282 [Source:HGNC Symbol;Acc:HGNC:53199]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370424","summary":null,"start":28783491,"end":28785787,"strand":-1,"description":"long intergenic non-protein coding RNA 2282 [Source:HGNC Symbol;Acc:HGNC:53199]"}, {"versioned_ensembl_gene_id":"ENSG00000127412.6","gene_symbol":"TRPV5","gene_name":"transient receptor potential cation channel subfamily V member 5 [Source:HGNC Symbol;Acc:HGNC:3145]","synonyms":"CaT2,ECAC1","biotype":"protein_coding","ncbi_id":"56302","summary":"This gene is a member of the transient receptor family and the TrpV subfamily. The calcium-selective channel encoded by this gene has 6 transmembrane-spanning domains, multiple potential phosphorylation sites, an N-linked glycosylation site, and 5 ANK repeats. This protein forms homotetramers or heterotetramers and is activated by a low internal calcium level. [provided by RefSeq, Jul 2008]","start":142908101,"end":142933808,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 5 [Source:HGNC Symbol;Acc:HGNC:3145]"}, {"versioned_ensembl_gene_id":"ENSG00000235022.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"LIRF,HZFw1","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30060589,"end":30066210,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000188937.5","gene_symbol":"NYX","gene_name":"nyctalopin [Source:HGNC Symbol;Acc:HGNC:8082]","synonyms":"CSNB4,CSNB1A,CSNB1,CLRP","biotype":"protein_coding","ncbi_id":"60506","summary":"The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008]","start":41447434,"end":41475710,"strand":1,"description":"nyctalopin [Source:HGNC Symbol;Acc:HGNC:8082]"}, {"versioned_ensembl_gene_id":"ENSG00000284708.1","gene_symbol":"AL031731.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11623558,"end":11643416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104529.17","gene_symbol":"EEF1D","gene_name":"eukaryotic translation elongation factor 1 delta [Source:HGNC Symbol;Acc:HGNC:3211]","synonyms":"FLJ20897,EF-1D","biotype":"protein_coding","ncbi_id":"1936","summary":"This gene encodes a subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This subunit, delta, functions as guanine nucleotide exchange factor. It is reported that following HIV-1 infection, this subunit interacts with HIV-1 Tat. This interaction results in repression of translation of host cell proteins and enhanced translation of viral proteins. Several alternatively spliced transcript variants encoding multiple isoforms have been found for this gene. Related pseudogenes have been defined on chromosomes 1, 6, 7, 9, 11, 13, 17, 19.[provided by RefSeq, Aug 2010]","start":143579697,"end":143599541,"strand":-1,"description":"eukaryotic translation elongation factor 1 delta [Source:HGNC Symbol;Acc:HGNC:3211]"}, {"versioned_ensembl_gene_id":"ENSG00000248916.1","gene_symbol":"NUP210P3","gene_name":"nucleoporin 210 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42712]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419070","summary":null,"start":129323046,"end":129325426,"strand":-1,"description":"nucleoporin 210 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42712]"}, {"versioned_ensembl_gene_id":"ENSG00000138399.17","gene_symbol":"FASTKD1","gene_name":"FAST kinase domains 1 [Source:HGNC Symbol;Acc:HGNC:26150]","synonyms":"FLJ21901","biotype":"protein_coding","ncbi_id":"79675","summary":null,"start":169529749,"end":169573875,"strand":-1,"description":"FAST kinase domains 1 [Source:HGNC Symbol;Acc:HGNC:26150]"}, {"versioned_ensembl_gene_id":"ENSG00000172671.19","gene_symbol":"ZFAND4","gene_name":"zinc finger AN1-type containing 4 [Source:HGNC Symbol;Acc:HGNC:23504]","synonyms":"ANUBL1,FLJ40185","biotype":"protein_coding","ncbi_id":"93550","summary":null,"start":45615501,"end":45672780,"strand":-1,"description":"zinc finger AN1-type containing 4 [Source:HGNC Symbol;Acc:HGNC:23504]"}, {"versioned_ensembl_gene_id":"ENSG00000254073.1","gene_symbol":"IGLVVII-41-1","gene_name":"immunoglobulin lambda variable (VII)-41-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15691]","synonyms":"IGLV(VII)-41-1","biotype":"IG_V_pseudogene","ncbi_id":"84089","summary":null,"start":22398849,"end":22398999,"strand":1,"description":"immunoglobulin lambda variable (VII)-41-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15691]"}, {"versioned_ensembl_gene_id":"ENSG00000214815.2","gene_symbol":"IMPDH1P3","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33958]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"136307","summary":null,"start":138440690,"end":138442238,"strand":1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33958]"}, {"versioned_ensembl_gene_id":"ENSG00000255690.2","gene_symbol":"TRIL","gene_name":"TLR4 interactor with leucine rich repeats [Source:HGNC Symbol;Acc:HGNC:22200]","synonyms":"KIAA0644","biotype":"protein_coding","ncbi_id":"9865","summary":"TRIL is a component of the TLR4 (MIM 603030) complex and is induced in a number of cell types by lipopolysaccharide (LPS) (Carpenter et al., 2009 [PubMed 19710467]).[supplied by OMIM, Apr 2010]","start":28953358,"end":28958292,"strand":-1,"description":"TLR4 interactor with leucine rich repeats [Source:HGNC Symbol;Acc:HGNC:22200]"}, {"versioned_ensembl_gene_id":"ENSG00000282015.1","gene_symbol":"AC004099.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37458806,"end":37459566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238015.2","gene_symbol":"AC104837.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78666272,"end":78666695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180016.2","gene_symbol":"OR1E1","gene_name":"olfactory receptor family 1 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:8189]","synonyms":"OR1E9P,OR1E6,OR1E5,OR17-32,OR17-2,OR13-66,HGM071","biotype":"protein_coding","ncbi_id":"8387","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3397104,"end":3398410,"strand":-1,"description":"olfactory receptor family 1 subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:8189]"}, {"versioned_ensembl_gene_id":"ENSG00000244094.1","gene_symbol":"SPRR2F","gene_name":"small proline rich protein 2F [Source:HGNC Symbol;Acc:HGNC:11266]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6705","summary":null,"start":153112114,"end":153113515,"strand":-1,"description":"small proline rich protein 2F [Source:HGNC Symbol;Acc:HGNC:11266]"}, {"versioned_ensembl_gene_id":"ENSG00000248880.1","gene_symbol":"ICE2P1","gene_name":"interactor of little elongation complex ELL subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48856]","synonyms":"NARG2P1","biotype":"processed_pseudogene","ncbi_id":"644491","summary":null,"start":188387471,"end":188389666,"strand":-1,"description":"interactor of little elongation complex ELL subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48856]"}, {"versioned_ensembl_gene_id":"ENSG00000237024.1","gene_symbol":"RPL21P33","gene_name":"ribosomal protein L21 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36686]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270953","summary":null,"start":60852260,"end":60852743,"strand":1,"description":"ribosomal protein L21 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36686]"}, {"versioned_ensembl_gene_id":"ENSG00000196805.7","gene_symbol":"SPRR2B","gene_name":"small proline rich protein 2B [Source:HGNC Symbol;Acc:HGNC:11262]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6701","summary":null,"start":153070224,"end":153070840,"strand":-1,"description":"small proline rich protein 2B [Source:HGNC Symbol;Acc:HGNC:11262]"}, {"versioned_ensembl_gene_id":"ENSG00000225342.2","gene_symbol":"AC079630.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40186009,"end":40224915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229899.1","gene_symbol":"AC084290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40286289,"end":40286662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267129.1","gene_symbol":"AC087498.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3377527,"end":3377602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149635.2","gene_symbol":"OCSTAMP","gene_name":"osteoclast stimulatory transmembrane protein [Source:HGNC Symbol;Acc:HGNC:16116]","synonyms":"dJ257E24.3,C20orf123","biotype":"protein_coding","ncbi_id":"128506","summary":"The protein encoded by this gene is orthologous to the mouse osteoclast stimulatory transmembrane protein (OCSTAMP), which is a membrane-anchored cell surface receptor that promotes nucleation of osteoclasts. The mouse protein is also involved in bone resorption and osteoclast differentiation. [provided by RefSeq, Feb 2017]","start":46540946,"end":46550574,"strand":-1,"description":"osteoclast stimulatory transmembrane protein [Source:HGNC Symbol;Acc:HGNC:16116]"}, {"versioned_ensembl_gene_id":"ENSG00000173171.14","gene_symbol":"MTX1","gene_name":"metaxin 1 [Source:HGNC Symbol;Acc:HGNC:7504]","synonyms":"MTXN,MTX","biotype":"protein_coding","ncbi_id":"4580","summary":null,"start":155208699,"end":155213824,"strand":1,"description":"metaxin 1 [Source:HGNC Symbol;Acc:HGNC:7504]"}, {"versioned_ensembl_gene_id":"ENSG00000159082.17","gene_symbol":"SYNJ1","gene_name":"synaptojanin 1 [Source:HGNC Symbol;Acc:HGNC:11503]","synonyms":"PARK20,INPP5G","biotype":"protein_coding","ncbi_id":"8867","summary":"This gene encodes a phosphoinositide phosphatase that regulates levels of membrane phosphatidylinositol-4,5-bisphosphate. As such, expression of this enzyme may affect synaptic transmission and membrane trafficking. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":32628759,"end":32728048,"strand":-1,"description":"synaptojanin 1 [Source:HGNC Symbol;Acc:HGNC:11503]"}, {"versioned_ensembl_gene_id":"ENSG00000094631.18","gene_symbol":"HDAC6","gene_name":"histone deacetylase 6 [Source:HGNC Symbol;Acc:HGNC:14064]","synonyms":"PPP1R90,KIAA0901,JM21,HD6,FLJ16239","biotype":"protein_coding","ncbi_id":"10013","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It contains an internal duplication of two catalytic domains which appear to function independently of each other. This protein possesses histone deacetylase activity and represses transcription. [provided by RefSeq, Jul 2008]","start":48801377,"end":48824982,"strand":1,"description":"histone deacetylase 6 [Source:HGNC Symbol;Acc:HGNC:14064]"}, {"versioned_ensembl_gene_id":"ENSG00000225310.1","gene_symbol":"DNAJC19P4","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45067]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480691","summary":null,"start":2985231,"end":2985575,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45067]"}, {"versioned_ensembl_gene_id":"ENSG00000169763.14","gene_symbol":"PRYP3","gene_name":"PTPN13-like, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34020]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442865","summary":null,"start":23681440,"end":23694579,"strand":-1,"description":"PTPN13-like, Y-linked pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:34020]"}, {"versioned_ensembl_gene_id":"ENSG00000280303.2","gene_symbol":"AC067931.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140636281,"end":140638283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244674.1","gene_symbol":"RPS3AP15","gene_name":"ribosomal protein S3a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652670","summary":null,"start":75542149,"end":75542929,"strand":-1,"description":"ribosomal protein S3a pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:35781]"}, {"versioned_ensembl_gene_id":"ENSG00000243794.1","gene_symbol":"SNRPCP10","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49825]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481701","summary":null,"start":75521803,"end":75522012,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49825]"}, {"versioned_ensembl_gene_id":"ENSG00000279421.1","gene_symbol":"AC067863.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78599892,"end":78600013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125966.9","gene_symbol":"MMP24","gene_name":"matrix metallopeptidase 24 [Source:HGNC Symbol;Acc:HGNC:7172]","synonyms":"MT5-MMP","biotype":"protein_coding","ncbi_id":"10893","summary":"This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. The encoded preproprotein is proteolytically processed to generate the mature protease. Unlike most MMPs, which are secreted, this protease is a member of the membrane-type MMP (MT-MMP) subfamily, contains a transmembrane domain and is expressed at the cell surface. Substrates of this protease include the proteins cadherin 2 and matrix metallopeptidase 2 (also known as 72 kDa type IV collagenase). The gene has previously been referred to as MMP25 but has been renamed matrix metallopeptidase 24 (MMP24). [provided by RefSeq, Oct 2019]","start":35226654,"end":35277000,"strand":1,"description":"matrix metallopeptidase 24 [Source:HGNC Symbol;Acc:HGNC:7172]"}, {"versioned_ensembl_gene_id":"ENSG00000236012.2","gene_symbol":"HIGD1AP12","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:43007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130383","summary":null,"start":111380291,"end":111380571,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:43007]"}, {"versioned_ensembl_gene_id":"ENSG00000145423.4","gene_symbol":"SFRP2","gene_name":"secreted frizzled related protein 2 [Source:HGNC Symbol;Acc:HGNC:10777]","synonyms":"SDF-5,SARP1,FRP-2","biotype":"protein_coding","ncbi_id":"6423","summary":"This gene encodes a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins. SFRPs act as soluble modulators of Wnt signaling. Methylation of this gene is a potential marker for the presence of colorectal cancer. [provided by RefSeq, Jul 2008]","start":153780592,"end":153789120,"strand":-1,"description":"secreted frizzled related protein 2 [Source:HGNC Symbol;Acc:HGNC:10777]"}, {"versioned_ensembl_gene_id":"ENSG00000233328.3","gene_symbol":"PFN1P1","gene_name":"profilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42989]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730138","summary":null,"start":171670517,"end":171670939,"strand":-1,"description":"profilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42989]"}, {"versioned_ensembl_gene_id":"ENSG00000196209.12","gene_symbol":"SIRPB2","gene_name":"signal regulatory protein beta 2 [Source:HGNC Symbol;Acc:HGNC:16247]","synonyms":"PTPNS1L3,PTPN1L,dJ776F14.2","biotype":"protein_coding","ncbi_id":"284759","summary":null,"start":1470741,"end":1491587,"strand":-1,"description":"signal regulatory protein beta 2 [Source:HGNC Symbol;Acc:HGNC:16247]"}, {"versioned_ensembl_gene_id":"ENSG00000169469.8","gene_symbol":"SPRR1B","gene_name":"small proline rich protein 1B [Source:HGNC Symbol;Acc:HGNC:11260]","synonyms":"SPRR1,GADD33","biotype":"protein_coding","ncbi_id":"6699","summary":"The protein encoded by this gene is an envelope protein of keratinocytes. The encoded protein is crosslinked to membrane proteins by transglutaminase, forming an insoluble layer under the plasma membrane. This protein is proline-rich and contains several tandem amino acid repeats. [provided by RefSeq, Nov 2015]","start":153031202,"end":153032900,"strand":1,"description":"small proline rich protein 1B [Source:HGNC Symbol;Acc:HGNC:11260]"}, {"versioned_ensembl_gene_id":"ENSG00000111269.2","gene_symbol":"CREBL2","gene_name":"cAMP responsive element binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:2350]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1389","summary":"cAMP response element (CRE)-binding protein-like-2 (CREBL2) was identified in a search to find genes in a commonly deleted region on chromosome 12p13 flanked by ETV6 and CDKN1B genes, frequently associated with hematopoietic malignancies, as well as breast, non-small-cell lung and ovarian cancers. CREBL2 shares a 41% identity with CRE-binding protein (CREB) over a 48-base long region which encodes the bZip domain of CREB. The bZip domain consists of about 30 amino acids rich in basic residues involved in DNA binding, followed by a leucine zipper motif involved in protein dimerization. This suggests that CREBL2 encodes a protein with DNA binding capabilities. The occurance of CREBL2 deletion in malignancy suggests that CREBL2 may act as a tumor suppressor gene. [provided by RefSeq, Jul 2008]","start":12611827,"end":12645108,"strand":1,"description":"cAMP responsive element binding protein like 2 [Source:HGNC Symbol;Acc:HGNC:2350]"}, {"versioned_ensembl_gene_id":"ENSG00000233837.1","gene_symbol":"EIF3LP2","gene_name":"eukaryotic translation initiation factor 3 subunit L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24657]","synonyms":"EIF3S6IPP2,EIF3EIPP2","biotype":"processed_pseudogene","ncbi_id":"143341","summary":null,"start":42566677,"end":42567483,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24657]"}, {"versioned_ensembl_gene_id":"ENSG00000255142.1","gene_symbol":"AP006621.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":781645,"end":782105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261127.2","gene_symbol":"AC133548.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32289547,"end":32310555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166199.12","gene_symbol":"ALKBH3","gene_name":"alkB homolog 3, alpha-ketoglutaratedependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:30141]","synonyms":"DEPC-1","biotype":"protein_coding","ncbi_id":"221120","summary":"The Escherichia coli AlkB protein protects against the cytotoxicity of methylating agents by repair of the specific DNA lesions generated in single-stranded DNA. ALKBH2 (MIM 610602) and ALKBH3 are E. coli AlkB homologs that catalyze the removal of 1-methyladenine and 3-methylcytosine (Duncan et al., 2002 [PubMed 12486230]).[supplied by OMIM, Mar 2008]","start":43880811,"end":43920266,"strand":1,"description":"alkB homolog 3, alpha-ketoglutaratedependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:30141]"}, {"versioned_ensembl_gene_id":"ENSG00000277729.1","gene_symbol":"GU182352.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54785929,"end":54797435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259822.2","gene_symbol":"AC140878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32278866,"end":32279115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245648.1","gene_symbol":"AC022075.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10363769,"end":10398506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272690.5","gene_symbol":"LINC02018","gene_name":"long intergenic non-protein coding RNA 2018 [Source:HGNC Symbol;Acc:HGNC:52853]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986100","summary":null,"start":75435348,"end":75457486,"strand":1,"description":"long intergenic non-protein coding RNA 2018 [Source:HGNC Symbol;Acc:HGNC:52853]"}, {"versioned_ensembl_gene_id":"ENSG00000202508.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":13511206,"end":13511313,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000034971.16","gene_symbol":"MYOC","gene_name":"myocilin [Source:HGNC Symbol;Acc:HGNC:7610]","synonyms":"TIGR,JOAG1,GLC1A","biotype":"protein_coding","ncbi_id":"4653","summary":"MYOC encodes the protein myocilin, which is believed to have a role in cytoskeletal function. MYOC is expressed in many occular tissues, including the trabecular meshwork, and was revealed to be the trabecular meshwork glucocorticoid-inducible response protein (TIGR). The trabecular meshwork is a specialized eye tissue essential in regulating intraocular pressure, and mutations in MYOC have been identified as the cause of hereditary juvenile-onset open-angle glaucoma. [provided by RefSeq, Jul 2008]","start":171635417,"end":171652683,"strand":-1,"description":"myocilin [Source:HGNC Symbol;Acc:HGNC:7610]"}, {"versioned_ensembl_gene_id":"ENSG00000261318.1","gene_symbol":"AC055855.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66278498,"end":66293357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239959.1","gene_symbol":"ENPP7P2","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48685]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421813","summary":null,"start":75446769,"end":75491202,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48685]"}, {"versioned_ensembl_gene_id":"ENSG00000118276.11","gene_symbol":"B4GALT6","gene_name":"beta-1,4-galactosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:929]","synonyms":"beta4GalT-VI","biotype":"protein_coding","ncbi_id":"9331","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes in human. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. This gene produces multiple protein isoforms - some of which are predicted to lack the N-terminal hydrophobic signal sequence and transmembrane domain. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. The canonical enzyme encoded by this gene is a lactosylceramide synthase important for glycolipid biosynthesis. [provided by RefSeq, Jan 2020]","start":31622247,"end":31685836,"strand":-1,"description":"beta-1,4-galactosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:929]"}, {"versioned_ensembl_gene_id":"ENSG00000188828.11","gene_symbol":"GLRA4","gene_name":"glycine receptor alpha 4 [Source:HGNC Symbol;Acc:HGNC:31715]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441509","summary":"This gene encodes a glycine receptor and member of the ligand-gated ion channel family of proteins. The encoded protein is missing the fourth transmembrane region compared to related proteins in mouse and rat, and experimental data suggests that the human protein is functionally inactive. However, there is strong evidence to support transcription of this gene. As a result, RefSeq, in collaboration with Ensembl-GENCODE, has determined that this locus is best described as a transcribed pseudogene. [provided by RefSeq, Aug 2019]","start":103707224,"end":103728655,"strand":-1,"description":"glycine receptor alpha 4 [Source:HGNC Symbol;Acc:HGNC:31715]"}, {"versioned_ensembl_gene_id":"ENSG00000122026.10","gene_symbol":"RPL21","gene_name":"ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:10313]","synonyms":"MGC71252,MGC104275,MGC104274,L21,FLJ27458,DKFZp686C06101","biotype":"protein_coding","ncbi_id":"6144","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L21E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":27251309,"end":27256691,"strand":1,"description":"ribosomal protein L21 [Source:HGNC Symbol;Acc:HGNC:10313]"}, {"versioned_ensembl_gene_id":"ENSG00000281038.1","gene_symbol":"OR8U1","gene_name":"olfactory receptor family 8 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:19611]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219417","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56383230,"end":56384159,"strand":1,"description":"olfactory receptor family 8 subfamily U member 1 [Source:HGNC Symbol;Acc:HGNC:19611]"}, {"versioned_ensembl_gene_id":"ENSG00000224707.1","gene_symbol":"E2F3-IT1","gene_name":"E2F3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41329]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874268","summary":null,"start":20437821,"end":20440178,"strand":1,"description":"E2F3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41329]"}, {"versioned_ensembl_gene_id":"ENSG00000255419.5","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31748922,"end":31755608,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000232862.5","gene_symbol":"AL138787.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":36080066,"end":36084026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206470.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29486547,"end":29487683,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000263366.2","gene_symbol":"ABHD17AP5","gene_name":"abhydrolase domain containing 17A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:34043]","synonyms":"FAM108A6P,FAM108A6","biotype":"processed_pseudogene","ncbi_id":"91219","summary":"This locus is a pseudogene in the FAM108 family, and lies in the immunoglobulin lambda gene cluster on chromosome 22q11.21. [provided by RefSeq, Jun 2010]","start":22114844,"end":22118005,"strand":-1,"description":"abhydrolase domain containing 17A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:34043]"}, {"versioned_ensembl_gene_id":"ENSG00000236323.1","gene_symbol":"BMP6P1","gene_name":"bone morphogenetic protein 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19329]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266700","summary":null,"start":22185941,"end":22186619,"strand":1,"description":"bone morphogenetic protein 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19329]"}, {"versioned_ensembl_gene_id":"ENSG00000159423.16","gene_symbol":"ALDH4A1","gene_name":"aldehyde dehydrogenase 4 family member A1 [Source:HGNC Symbol;Acc:HGNC:406]","synonyms":"P5CDh,ALDH4","biotype":"protein_coding","ncbi_id":"8659","summary":"This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009]","start":18871430,"end":18902781,"strand":-1,"description":"aldehyde dehydrogenase 4 family member A1 [Source:HGNC Symbol;Acc:HGNC:406]"}, {"versioned_ensembl_gene_id":"ENSG00000236671.7","gene_symbol":"PRKG1-AS1","gene_name":"PRKG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45029]","synonyms":"RP11-573I11.2","biotype":"antisense_RNA","ncbi_id":"100506939","summary":null,"start":52230742,"end":52314128,"strand":-1,"description":"PRKG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:45029]"}, {"versioned_ensembl_gene_id":"ENSG00000188167.8","gene_symbol":"TMPPE","gene_name":"transmembrane protein with metallophosphoesterase domain [Source:HGNC Symbol;Acc:HGNC:33865]","synonyms":"FLJ45032","biotype":"protein_coding","ncbi_id":"643853","summary":null,"start":33090421,"end":33096801,"strand":-1,"description":"transmembrane protein with metallophosphoesterase domain [Source:HGNC Symbol;Acc:HGNC:33865]"}, {"versioned_ensembl_gene_id":"ENSG00000117643.14","gene_symbol":"MAN1C1","gene_name":"mannosidase alpha class 1C member 1 [Source:HGNC Symbol;Acc:HGNC:19080]","synonyms":"HMIC","biotype":"protein_coding","ncbi_id":"57134","summary":null,"start":25617468,"end":25786207,"strand":1,"description":"mannosidase alpha class 1C member 1 [Source:HGNC Symbol;Acc:HGNC:19080]"}, {"versioned_ensembl_gene_id":"ENSG00000177613.8","gene_symbol":"CSTF2T","gene_name":"cleavage stimulation factor subunit 2 tau variant [Source:HGNC Symbol;Acc:HGNC:17086]","synonyms":"tauCstF-64,KIAA0689,DKFZp434C1013,CstF-64T","biotype":"protein_coding","ncbi_id":"23283","summary":null,"start":51695487,"end":51699591,"strand":-1,"description":"cleavage stimulation factor subunit 2 tau variant [Source:HGNC Symbol;Acc:HGNC:17086]"}, {"versioned_ensembl_gene_id":"ENSG00000235279.1","gene_symbol":"AC069079.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51302566,"end":51306709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213659.4","gene_symbol":"RSU1P3","gene_name":"Ras suppressor protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44392]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419964","summary":null,"start":51319826,"end":51320660,"strand":1,"description":"Ras suppressor protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44392]"}, {"versioned_ensembl_gene_id":"ENSG00000240038.6","gene_symbol":"AMY2B","gene_name":"amylase, alpha 2B (pancreatic) [Source:HGNC Symbol;Acc:HGNC:478]","synonyms":"AMY2","biotype":"protein_coding","ncbi_id":"280","summary":"Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the pancreas. [provided by RefSeq, Jun 2013]","start":103553815,"end":103579534,"strand":1,"description":"amylase, alpha 2B (pancreatic) [Source:HGNC Symbol;Acc:HGNC:478]"}, {"versioned_ensembl_gene_id":"ENSG00000106089.11","gene_symbol":"STX1A","gene_name":"syntaxin 1A [Source:HGNC Symbol;Acc:HGNC:11433]","synonyms":"p35-1,HPC-1,STX1","biotype":"protein_coding","ncbi_id":"6804","summary":"This gene encodes a member of the syntaxin superfamily. Syntaxins are nervous system-specific proteins implicated in the docking of synaptic vesicles with the presynaptic plasma membrane. Syntaxins possess a single C-terminal transmembrane domain, a SNARE [Soluble NSF (N-ethylmaleimide-sensitive fusion protein)-Attachment protein REceptor] domain (known as H3), and an N-terminal regulatory domain (Habc). Syntaxins bind synaptotagmin in a calcium-dependent fashion and interact with voltage dependent calcium and potassium channels via the C-terminal H3 domain. This gene product is a key molecule in ion channel regulation and synaptic exocytosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":73699206,"end":73719672,"strand":-1,"description":"syntaxin 1A [Source:HGNC Symbol;Acc:HGNC:11433]"}, {"versioned_ensembl_gene_id":"ENSG00000243141.2","gene_symbol":"RPL23AP66","gene_name":"ribosomal protein L23a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271620","summary":null,"start":12338776,"end":12339254,"strand":1,"description":"ribosomal protein L23a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35940]"}, {"versioned_ensembl_gene_id":"ENSG00000176410.7","gene_symbol":"DNAJC30","gene_name":"DnaJ heat shock protein family (Hsp40) member C30 [Source:HGNC Symbol;Acc:HGNC:16410]","synonyms":"WBSCR18","biotype":"protein_coding","ncbi_id":"84277","summary":"This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]","start":73680969,"end":73683453,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C30 [Source:HGNC Symbol;Acc:HGNC:16410]"}, {"versioned_ensembl_gene_id":"ENSG00000161217.11","gene_symbol":"PCYT1A","gene_name":"phosphate cytidylyltransferase 1, choline, alpha [Source:HGNC Symbol;Acc:HGNC:8754]","synonyms":"PCYT1,CTPCT,CT","biotype":"protein_coding","ncbi_id":"5130","summary":"This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]","start":196214222,"end":196287957,"strand":-1,"description":"phosphate cytidylyltransferase 1, choline, alpha [Source:HGNC Symbol;Acc:HGNC:8754]"}, {"versioned_ensembl_gene_id":"ENSG00000171148.13","gene_symbol":"TADA3","gene_name":"transcriptional adaptor 3 [Source:HGNC Symbol;Acc:HGNC:19422]","synonyms":"TADA3L,NGG1,hADA3,FLJ21329,FLJ20221,ADA3","biotype":"protein_coding","ncbi_id":"10474","summary":"DNA-binding transcriptional activator proteins increase the rate of transcription by interacting with the transcriptional machinery bound to the basal promoter in conjunction with adaptor proteins, possibly by acetylation and destabilization of nucleosomes. The protein encoded by this gene is a transcriptional activator adaptor and a component of the histone acetyl transferase (HAT) coactivator complex which plays a crucial role in chromatin modulation and cell cycle progression. Along with the other components of the complex, this protein links transcriptional activators bound to specific promoters, to histone acetylation and the transcriptional machinery. The protein is also involved in the stabilization and activation of the p53 tumor suppressor protein that plays a role in the cellular response to DNA damage. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]","start":9779860,"end":9793011,"strand":-1,"description":"transcriptional adaptor 3 [Source:HGNC Symbol;Acc:HGNC:19422]"}, {"versioned_ensembl_gene_id":"ENSG00000115825.9","gene_symbol":"PRKD3","gene_name":"protein kinase D3 [Source:HGNC Symbol;Acc:HGNC:9408]","synonyms":"PRKCN,EPK2","biotype":"protein_coding","ncbi_id":"23683","summary":"This gene belongs to the multigene protein kinase D family of serine/threonine kinases, which bind diacylglycerol and phorbol esters. Members of this family are characterized by an N-terminal regulatory domain comprised of a tandem repeat of cysteine-rich zinc-finger motifs and a pleckstrin domain. The C-terminal region contains the catalytic domain and is distantly related to calcium-regulated kinases. Catalytic activity of this enzyme promotes its nuclear localization. This protein has been implicated in a variety of functions including negative regulation of human airway epithelial barrier formation, growth regulation of breast and prostate cancer cells, and vesicle trafficking. [provided by RefSeq, Jan 2015]","start":37250502,"end":37324808,"strand":-1,"description":"protein kinase D3 [Source:HGNC Symbol;Acc:HGNC:9408]"}, {"versioned_ensembl_gene_id":"ENSG00000272054.1","gene_symbol":"AC007390.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37208875,"end":37212677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198455.4","gene_symbol":"ZXDB","gene_name":"zinc finger, X-linked, duplicated B [Source:HGNC Symbol;Acc:HGNC:13199]","synonyms":"ZNF905","biotype":"protein_coding","ncbi_id":"158586","summary":"The ZXDB gene is one of a pair of duplicated zinc finger genes on chromosome Xp11.21 (Greig et al., 1993 [PubMed 8268913]); see also ZXDA (MIM 300235).[supplied by OMIM, Jul 2010]","start":57591652,"end":57597545,"strand":1,"description":"zinc finger, X-linked, duplicated B [Source:HGNC Symbol;Acc:HGNC:13199]"}, {"versioned_ensembl_gene_id":"ENSG00000137462.6","gene_symbol":"TLR2","gene_name":"toll like receptor 2 [Source:HGNC Symbol;Acc:HGNC:11848]","synonyms":"TIL4,CD282","biotype":"protein_coding","ncbi_id":"7097","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. This protein is a cell-surface protein that can form heterodimers with other TLR family members to recognize conserved molecules derived from microorganisms known as pathogen-associated molecular patterns (PAMPs). Activation of TLRs by PAMPs leads to an up-regulation of signaling pathways to modulate the host's inflammatory response. This gene is also thought to promote apoptosis in response to bacterial lipoproteins. This gene has been implicated in the pathogenesis of several autoimmune diseases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":153701500,"end":153705699,"strand":1,"description":"toll like receptor 2 [Source:HGNC Symbol;Acc:HGNC:11848]"}, {"versioned_ensembl_gene_id":"ENSG00000185745.9","gene_symbol":"IFIT1","gene_name":"interferon induced protein with tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:5407]","synonyms":"G10P1,IFNAI1,IFI56,GARG-16","biotype":"protein_coding","ncbi_id":"3434","summary":"This gene encodes a protein containing tetratricopeptide repeats that was originally identified as induced upon treatment with interferon. The encoded protein may inhibit viral replication and translational initiation. This gene is located in a cluster on chromosome 10 with five other closely related genes. There is a pseudogene for this gene on chromosome 13. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2012]","start":89392546,"end":89406486,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:5407]"}, {"versioned_ensembl_gene_id":"ENSG00000090512.11","gene_symbol":"FETUB","gene_name":"fetuin B [Source:HGNC Symbol;Acc:HGNC:3658]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26998","summary":"The protein encoded by this gene is a member of the fetuin family, part of the cystatin superfamily of cysteine protease inhibitors. Fetuins have been implicated in several diverse functions, including osteogenesis and bone resorption, regulation of the insulin and hepatocyte growth factor receptors, and response to systemic inflammation. This protein may be secreted by cells. [provided by RefSeq, Jul 2008]","start":186635969,"end":186653141,"strand":1,"description":"fetuin B [Source:HGNC Symbol;Acc:HGNC:3658]"}, {"versioned_ensembl_gene_id":"ENSG00000261478.1","gene_symbol":"AC013391.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89508961,"end":89510416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251279.1","gene_symbol":"SMIM15-AS1","gene_name":"SMIM15 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41293]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928630","summary":null,"start":61162070,"end":61232040,"strand":1,"description":"SMIM15 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41293]"}, {"versioned_ensembl_gene_id":"ENSG00000147548.16","gene_symbol":"NSD3","gene_name":"nuclear receptor binding SET domain protein 3 [Source:HGNC Symbol;Acc:HGNC:12767]","synonyms":"WHSC1L1,WHISTLE,KMT3F,FLJ20353","biotype":"protein_coding","ncbi_id":"54904","summary":"This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. Two alternatively spliced variants have been described. [provided by RefSeq, May 2015]","start":38269697,"end":38382272,"strand":-1,"description":"nuclear receptor binding SET domain protein 3 [Source:HGNC Symbol;Acc:HGNC:12767]"}, {"versioned_ensembl_gene_id":"ENSG00000185946.15","gene_symbol":"RNPC3","gene_name":"RNA binding region (RNP1, RRM) containing 3 [Source:HGNC Symbol;Acc:HGNC:18666]","synonyms":"SNRNP65,RBM40,KIAA1839,FLJ20008","biotype":"protein_coding","ncbi_id":"55599","summary":"Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 65K protein that is a component of the U12-type spliceosome. This protein contains two RNA recognition motifs (RRMs), suggesting that it may contact one of the small nuclear RNAs of the minor spliceosome. [provided by RefSeq, Jul 2008]","start":103525691,"end":103555239,"strand":1,"description":"RNA binding region (RNP1, RRM) containing 3 [Source:HGNC Symbol;Acc:HGNC:18666]"}, {"versioned_ensembl_gene_id":"ENSG00000248527.1","gene_symbol":"MTATP6P1","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44575]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480796","summary":null,"start":633696,"end":634376,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44575]"}, {"versioned_ensembl_gene_id":"ENSG00000065268.10","gene_symbol":"WDR18","gene_name":"WD repeat domain 18 [Source:HGNC Symbol;Acc:HGNC:17956]","synonyms":"Ipi3","biotype":"protein_coding","ncbi_id":"57418","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]","start":984271,"end":998438,"strand":1,"description":"WD repeat domain 18 [Source:HGNC Symbol;Acc:HGNC:17956]"}, {"versioned_ensembl_gene_id":"ENSG00000256944.1","gene_symbol":"AP003721.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60913166,"end":60914052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229905.1","gene_symbol":"AL669831.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":760911,"end":761989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196734.8","gene_symbol":"LCE1B","gene_name":"late cornified envelope 1B [Source:HGNC Symbol;Acc:HGNC:16611]","synonyms":"SPRL2A,LEP2","biotype":"protein_coding","ncbi_id":"353132","summary":null,"start":152811971,"end":152813109,"strand":1,"description":"late cornified envelope 1B [Source:HGNC Symbol;Acc:HGNC:16611]"}, {"versioned_ensembl_gene_id":"ENSG00000164190.17","gene_symbol":"NIPBL","gene_name":"NIPBL, cohesin loading factor [Source:HGNC Symbol;Acc:HGNC:28862]","synonyms":"Scc2,IDN3,FLJ13648,FLJ13354,FLJ12597,FLJ11203,DKFZp434L1319","biotype":"protein_coding","ncbi_id":"25836","summary":"This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and cognitive disability. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":36876759,"end":37066413,"strand":1,"description":"NIPBL, cohesin loading factor [Source:HGNC Symbol;Acc:HGNC:28862]"}, {"versioned_ensembl_gene_id":"ENSG00000179452.2","gene_symbol":"LINC01699","gene_name":"long intergenic non-protein coding RNA 1699 [Source:HGNC Symbol;Acc:HGNC:52487]","synonyms":"GM140","biotype":"lincRNA","ncbi_id":"100287948","summary":null,"start":181236388,"end":181238604,"strand":1,"description":"long intergenic non-protein coding RNA 1699 [Source:HGNC Symbol;Acc:HGNC:52487]"}, {"versioned_ensembl_gene_id":"ENSG00000110108.9","gene_symbol":"TMEM109","gene_name":"transmembrane protein 109 [Source:HGNC Symbol;Acc:HGNC:28771]","synonyms":"MGC5508","biotype":"protein_coding","ncbi_id":"79073","summary":null,"start":60913874,"end":60923443,"strand":1,"description":"transmembrane protein 109 [Source:HGNC Symbol;Acc:HGNC:28771]"}, {"versioned_ensembl_gene_id":"ENSG00000003509.15","gene_symbol":"NDUFAF7","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 7 [Source:HGNC Symbol;Acc:HGNC:28816]","synonyms":"PRO1853,MidA,C2orf56","biotype":"protein_coding","ncbi_id":"55471","summary":"This gene encodes an assembly factor protein which helps in the assembly and stabilization of Complex I, a large multi-subunit enzyme in the mitochondrial respiratory chain. Complex I is involved in several physiological activities in the cell, including metabolite transport and ATP synthesis. The encoded protein is a methyltransferase which methylates Arg85 of a subunit of Complex I in the early stages of its assembly. A pseudogene related to this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":37231631,"end":37253403,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 7 [Source:HGNC Symbol;Acc:HGNC:28816]"}, {"versioned_ensembl_gene_id":"ENSG00000140534.13","gene_symbol":"TICRR","gene_name":"TOPBP1 interacting checkpoint and replication regulator [Source:HGNC Symbol;Acc:HGNC:28704]","synonyms":"Treslin,SLD3,MGC45866,FLJ41618,C15orf42","biotype":"protein_coding","ncbi_id":"90381","summary":"Treslin is involved in the initiation of DNA replication (Kumagai et al., 2010 [PubMed 20116089]).[supplied by OMIM, Apr 2010]","start":89575482,"end":89631056,"strand":1,"description":"TOPBP1 interacting checkpoint and replication regulator [Source:HGNC Symbol;Acc:HGNC:28704]"}, {"versioned_ensembl_gene_id":"ENSG00000230585.2","gene_symbol":"PHBP12","gene_name":"prohibitin pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39291]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418820","summary":null,"start":50780340,"end":50781150,"strand":1,"description":"prohibitin pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39291]"}, {"versioned_ensembl_gene_id":"ENSG00000282588.1","gene_symbol":"AC069363.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36009598,"end":36011654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250189.2","gene_symbol":"AC097504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141405172,"end":141407586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241635.7","gene_symbol":"UGT1A1","gene_name":"UDP glucuronosyltransferase family 1 member A1 [Source:HGNC Symbol;Acc:HGNC:12530]","synonyms":"GNT1,UGT1A,UGT1","biotype":"protein_coding","ncbi_id":"54658","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The preferred substrate of this enzyme is bilirubin, although it also has moderate activity with simple phenols, flavones, and C18 steroids. Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome. [provided by RefSeq, Jul 2008]","start":233760248,"end":233773299,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A1 [Source:HGNC Symbol;Acc:HGNC:12530]"}, {"versioned_ensembl_gene_id":"ENSG00000248114.1","gene_symbol":"AC114812.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":233738952,"end":233741957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235146.2","gene_symbol":"AC114498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":587629,"end":594768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278303.4","gene_symbol":"MUC4","gene_name":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4585","summary":"The major constituents of mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection of the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted isoforms may exist. At least two dozen transcript variants of this gene have been found, although for many of them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) of 48 nt tandem repeats. [provided by RefSeq, Jul 2008]","start":195744993,"end":195789727,"strand":-1,"description":"mucin 4, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7514]"}, {"versioned_ensembl_gene_id":"ENSG00000268663.1","gene_symbol":"WBP1LP6","gene_name":"WW domain binding protein 1-like pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43956]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481797","summary":null,"start":674842,"end":675265,"strand":1,"description":"WW domain binding protein 1-like pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:43956]"}, {"versioned_ensembl_gene_id":"ENSG00000140505.6","gene_symbol":"CYP1A2","gene_name":"cytochrome P450 family 1 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2596]","synonyms":"P3-450,CP12","biotype":"protein_coding","ncbi_id":"1544","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The protein encoded by this gene localizes to the endoplasmic reticulum and its expression is induced by some polycyclic aromatic hydrocarbons (PAHs), some of which are found in cigarette smoke. The enzyme's endogenous substrate is unknown; however, it is able to metabolize some PAHs to carcinogenic intermediates. Other xenobiotic substrates for this enzyme include caffeine, aflatoxin B1, and acetaminophen. The transcript from this gene contains four Alu sequences flanked by direct repeats in the 3' untranslated region. [provided by RefSeq, Jul 2008]","start":74748844,"end":74756202,"strand":1,"description":"cytochrome P450 family 1 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2596]"}, {"versioned_ensembl_gene_id":"ENSG00000267585.1","gene_symbol":"AC013290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34573987,"end":34574523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116560.10","gene_symbol":"SFPQ","gene_name":"splicing factor proline and glutamine rich [Source:HGNC Symbol;Acc:HGNC:10774]","synonyms":"PSF,PPP1R140","biotype":"protein_coding","ncbi_id":"6421","summary":null,"start":35176378,"end":35193148,"strand":-1,"description":"splicing factor proline and glutamine rich [Source:HGNC Symbol;Acc:HGNC:10774]"}, {"versioned_ensembl_gene_id":"ENSG00000221955.10","gene_symbol":"SLC12A8","gene_name":"solute carrier family 12 member 8 [Source:HGNC Symbol;Acc:HGNC:15595]","synonyms":"CCC9","biotype":"protein_coding","ncbi_id":"84561","summary":"This gene is thought to be a candidate for psoriasis susceptibility. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2010]","start":125082636,"end":125212864,"strand":-1,"description":"solute carrier family 12 member 8 [Source:HGNC Symbol;Acc:HGNC:15595]"}, {"versioned_ensembl_gene_id":"ENSG00000237130.1","gene_symbol":"MRPS6P2","gene_name":"mitochondrial ribosomal protein S6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359781","summary":null,"start":50846468,"end":50846837,"strand":1,"description":"mitochondrial ribosomal protein S6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:29781]"}, {"versioned_ensembl_gene_id":"ENSG00000078668.13","gene_symbol":"VDAC3","gene_name":"voltage dependent anion channel 3 [Source:HGNC Symbol;Acc:HGNC:12674]","synonyms":"HD-VDAC3","biotype":"protein_coding","ncbi_id":"7419","summary":"This gene encodes a voltage-dependent anion channel (VDAC), and belongs to the mitochondrial porin family. VDACs are small, integral membrane proteins that traverse the outer mitochondrial membrane and conduct ATP and other small metabolites. They are known to bind several kinases of intermediary metabolism, thought to be involved in translocation of adenine nucleotides, and are hypothesized to form part of the mitochondrial permeability transition pore, which results in the release of cytochrome c at the onset of apoptotic cell death. Alternatively transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":42391624,"end":42405897,"strand":1,"description":"voltage dependent anion channel 3 [Source:HGNC Symbol;Acc:HGNC:12674]"}, {"versioned_ensembl_gene_id":"ENSG00000276702.1","gene_symbol":"AC010809.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33850538,"end":33851178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118804.8","gene_symbol":"STBD1","gene_name":"starch binding domain 1 [Source:HGNC Symbol;Acc:HGNC:24854]","synonyms":"GENX-3414,FLJ41801","biotype":"protein_coding","ncbi_id":"8987","summary":null,"start":76306026,"end":76311599,"strand":1,"description":"starch binding domain 1 [Source:HGNC Symbol;Acc:HGNC:24854]"}, {"versioned_ensembl_gene_id":"ENSG00000232102.1","gene_symbol":"MTCO3P2","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39681]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873207","summary":null,"start":23765934,"end":23766104,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39681]"}, {"versioned_ensembl_gene_id":"ENSG00000249162.1","gene_symbol":"ADAM20P3","gene_name":"ADAM metallopeptidase domain 20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43902]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644325","summary":null,"start":187746094,"end":187748199,"strand":-1,"description":"ADAM metallopeptidase domain 20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43902]"}, {"versioned_ensembl_gene_id":"ENSG00000185104.19","gene_symbol":"FAF1","gene_name":"Fas associated factor 1 [Source:HGNC Symbol;Acc:HGNC:3578]","synonyms":"HFAF1s,hFAF1,CGI-03,UBXN3A,UBXD12","biotype":"protein_coding","ncbi_id":"11124","summary":"Interaction of Fas ligand (TNFSF6) with the FAS antigen (TNFRSF6) mediates programmed cell death, also called apoptosis, in a number of organ systems. The protein encoded by this gene binds to FAS antigen and can initiate apoptosis or enhance apoptosis initiated through FAS antigen. Initiation of apoptosis by the protein encoded by this gene requires a ubiquitin-like domain but not the FAS-binding domain. [provided by RefSeq, Jul 2008]","start":50437028,"end":50960263,"strand":-1,"description":"Fas associated factor 1 [Source:HGNC Symbol;Acc:HGNC:3578]"}, {"versioned_ensembl_gene_id":"ENSG00000233505.1","gene_symbol":"KRT18P1","gene_name":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]","synonyms":"dJ25J6.3","biotype":"processed_pseudogene","ncbi_id":"3879","summary":null,"start":28965658,"end":28966988,"strand":-1,"description":"keratin 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6434]"}, {"versioned_ensembl_gene_id":"ENSG00000272632.1","gene_symbol":"AC097504.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141430831,"end":141431284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225767.1","gene_symbol":"AL049637.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50461469,"end":50471150,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260649.1","gene_symbol":"AC133485.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32189262,"end":32189481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228755.1","gene_symbol":"PABPC1P8","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37988]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132766","summary":null,"start":42279734,"end":42281819,"strand":-1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37988]"}, {"versioned_ensembl_gene_id":"ENSG00000282521.1","gene_symbol":"CCL15-CCL14","gene_name":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]","synonyms":null,"biotype":"protein_coding","ncbi_id":"348249","summary":"A cluster of CC chemokine genes exists on chromosome 17q11.2. The CC chemokines are secreted proteins characterized by two adjacent cysteines. The genes chemokine (C-C motif) ligand 14 and chemokine (C-C motif) ligand 15 are adjacent loci and express read-through transcripts spanning both loci. The read-through transcripts were originally interpreted as bicistronic transcripts, but they are represented as non-coding because they are candidates for nonsense-mediated mRNA decay (NMD). [provided by RefSeq, Dec 2009]","start":35983688,"end":36001656,"strand":-1,"description":"CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]"}, {"versioned_ensembl_gene_id":"ENSG00000188064.9","gene_symbol":"WNT7B","gene_name":"Wnt family member 7B [Source:HGNC Symbol;Acc:HGNC:12787]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7477","summary":"This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Among members of the human WNT family, this gene product is most similar to WNT7A protein. [provided by RefSeq, Oct 2008]","start":45920362,"end":45977129,"strand":-1,"description":"Wnt family member 7B [Source:HGNC Symbol;Acc:HGNC:12787]"}, {"versioned_ensembl_gene_id":"ENSG00000282446.1","gene_symbol":"AC004675.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35983688,"end":35990302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239940.1","gene_symbol":"AL662865.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28983392,"end":28985128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227380.2","gene_symbol":"HCG15","gene_name":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]","synonyms":"dJ25J6.6,HCG16,dJ25J6.7","biotype":"processed_transcript","ncbi_id":"414761","summary":null,"start":28982795,"end":28984076,"strand":1,"description":"HLA complex group 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18361]"}, {"versioned_ensembl_gene_id":"ENSG00000250141.1","gene_symbol":"LINC02276","gene_name":"long intergenic non-protein coding RNA 2276 [Source:HGNC Symbol;Acc:HGNC:53192]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377456","summary":null,"start":141569931,"end":141576077,"strand":-1,"description":"long intergenic non-protein coding RNA 2276 [Source:HGNC Symbol;Acc:HGNC:53192]"}, {"versioned_ensembl_gene_id":"ENSG00000253668.1","gene_symbol":"AC103778.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53712697,"end":53712896,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260540.2","gene_symbol":"ABHD17AP8","gene_name":"abhydrolase domain containing 17A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38509]","synonyms":"FAM108A9P","biotype":"unprocessed_pseudogene","ncbi_id":"647144","summary":null,"start":32199902,"end":32202822,"strand":1,"description":"abhydrolase domain containing 17A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38509]"}, {"versioned_ensembl_gene_id":"ENSG00000234467.1","gene_symbol":"SLC25A1P2","gene_name":"solute carrier family 25 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43847]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133079","summary":null,"start":63398046,"end":63398957,"strand":1,"description":"solute carrier family 25 member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43847]"}, {"versioned_ensembl_gene_id":"ENSG00000170373.8","gene_symbol":"CST1","gene_name":"cystatin SN [Source:HGNC Symbol;Acc:HGNC:2473]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1469","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a cysteine proteinase inhibitor found in saliva, tears, urine, and seminal fluid. [provided by RefSeq, Jul 2008]","start":23747553,"end":23751268,"strand":-1,"description":"cystatin SN [Source:HGNC Symbol;Acc:HGNC:2473]"}, {"versioned_ensembl_gene_id":"ENSG00000280121.1","gene_symbol":"AC010335.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18448275,"end":18448805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076770.14","gene_symbol":"MBNL3","gene_name":"muscleblind like splicing regulator 3 [Source:HGNC Symbol;Acc:HGNC:20564]","synonyms":"MBLX39,FLJ11316,CHCR,MBXL","biotype":"protein_coding","ncbi_id":"55796","summary":"This gene encodes a member of the muscleblind-like family of proteins. The encoded protein may function in regulation of alternative splicing and may play a role in the pathophysiology of myotonic dystrophy. Alternatively spliced transcript variants have been described. [provided by RefSeq, Dec 2009]","start":132369317,"end":132489968,"strand":-1,"description":"muscleblind like splicing regulator 3 [Source:HGNC Symbol;Acc:HGNC:20564]"}, {"versioned_ensembl_gene_id":"ENSG00000248019.2","gene_symbol":"FAM13A-AS1","gene_name":"FAM13A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19370]","synonyms":"NCRNA00039,FAM13AOS,FAM13A1OS","biotype":"antisense_RNA","ncbi_id":"285512","summary":null,"start":88709789,"end":88730103,"strand":1,"description":"FAM13A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:19370]"}, {"versioned_ensembl_gene_id":"ENSG00000223889.1","gene_symbol":"AC073188.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63393749,"end":63394109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248552.1","gene_symbol":"AC074344.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159375099,"end":159375322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242435.1","gene_symbol":"UPK3BP1","gene_name":"uroplakin 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42353]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"107080637","summary":null,"start":77004662,"end":77005774,"strand":1,"description":"uroplakin 3B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42353]"}, {"versioned_ensembl_gene_id":"ENSG00000188000.4","gene_symbol":"OR7D2","gene_name":"olfactory receptor family 7 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8378]","synonyms":"OR19-4,HTPCRH03,FLJ38149","biotype":"protein_coding","ncbi_id":"162998","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":9178979,"end":9188817,"strand":1,"description":"olfactory receptor family 7 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8378]"}, {"versioned_ensembl_gene_id":"ENSG00000235169.7","gene_symbol":"SMIM1","gene_name":"small integral membrane protein 1 (Vel blood group) [Source:HGNC Symbol;Acc:HGNC:44204]","synonyms":"Vel","biotype":"protein_coding","ncbi_id":"388588","summary":"This gene encodes a small, conserved protein that participates in red blood cell formation. The encoded protein is localized to the cell membrane and is the antigen for the Vel blood group. Alternative splicing results in different transcript variants that encode the same protein. [provided by RefSeq, Dec 2013]","start":3772788,"end":3775982,"strand":1,"description":"small integral membrane protein 1 (Vel blood group) [Source:HGNC Symbol;Acc:HGNC:44204]"}, {"versioned_ensembl_gene_id":"ENSG00000267418.1","gene_symbol":"ELOCP29","gene_name":"elongin C pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:49170]","synonyms":"TCEB1P29","biotype":"processed_pseudogene","ncbi_id":"100132973","summary":null,"start":9182369,"end":9183048,"strand":-1,"description":"elongin C pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:49170]"}, {"versioned_ensembl_gene_id":"ENSG00000280543.1","gene_symbol":"ASAP1-IT2","gene_name":"ASAP1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:48917]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100507117","summary":null,"start":130082738,"end":130084768,"strand":-1,"description":"ASAP1 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:48917]"}, {"versioned_ensembl_gene_id":"ENSG00000232934.7","gene_symbol":"AL157786.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112395813,"end":112425589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224301.1","gene_symbol":"AL590502.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63123938,"end":63125537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123009.4","gene_symbol":"NME2P1","gene_name":"NME/NM23 nucleoside diphosphate kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31358]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"283458","summary":null,"start":120282303,"end":120282716,"strand":1,"description":"NME/NM23 nucleoside diphosphate kinase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31358]"}, {"versioned_ensembl_gene_id":"ENSG00000267213.4","gene_symbol":"AC007773.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32390050,"end":32405560,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196664.4","gene_symbol":"TLR7","gene_name":"toll like receptor 7 [Source:HGNC Symbol;Acc:HGNC:15631]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51284","summary":"The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. The human TLR family comprises 11 members. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. For the recognition of structural components in foreign microorganisms, the various TLRs exhibit different patterns of expression as well; in this way for example, TLR-3, -7, and -8 are essential in the recognition of single-stranded RNA viruses. TLR7 senses single-stranded RNA oligonucleotides containing guanosine- and uridine-rich sequences from RNA viruses, a recognition occuring in the endosomes of plasmacytoid dendritic cells and B cells. This gene is predominantly expressed in lung, placenta, and spleen, and is phylogenetically related and lies in close proximity to another family member, TLR8, on chromosome X. [provided by RefSeq, Aug 2020]","start":12867083,"end":12890380,"strand":1,"description":"toll like receptor 7 [Source:HGNC Symbol;Acc:HGNC:15631]"}, {"versioned_ensembl_gene_id":"ENSG00000147576.15","gene_symbol":"ADHFE1","gene_name":"alcohol dehydrogenase, iron containing 1 [Source:HGNC Symbol;Acc:HGNC:16354]","synonyms":"FLJ32430,ADHFe1","biotype":"protein_coding","ncbi_id":"137872","summary":"The ADHFE1 gene encodes hydroxyacid-oxoacid transhydrogenase (EC 1.1.99.24), which is responsible for the oxidation of 4-hydroxybutyrate in mammalian tissues (Kardon et al., 2006 [PubMed 16616524]).[supplied by OMIM, Mar 2008]","start":66430185,"end":66471601,"strand":1,"description":"alcohol dehydrogenase, iron containing 1 [Source:HGNC Symbol;Acc:HGNC:16354]"}, {"versioned_ensembl_gene_id":"ENSG00000253623.1","gene_symbol":"AC009879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66480648,"end":66481486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179041.3","gene_symbol":"RRS1","gene_name":"ribosome biogenesis regulator homolog [Source:HGNC Symbol;Acc:HGNC:17083]","synonyms":"KIAA0112","biotype":"protein_coding","ncbi_id":"23212","summary":null,"start":66429028,"end":66430733,"strand":1,"description":"ribosome biogenesis regulator homolog [Source:HGNC Symbol;Acc:HGNC:17083]"}, {"versioned_ensembl_gene_id":"ENSG00000229111.1","gene_symbol":"MED4-AS1","gene_name":"MED4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39213]","synonyms":"MED4-AS","biotype":"antisense_RNA","ncbi_id":"100873965","summary":null,"start":48077137,"end":48079991,"strand":1,"description":"MED4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39213]"}, {"versioned_ensembl_gene_id":"ENSG00000064961.18","gene_symbol":"HMG20B","gene_name":"high mobility group 20B [Source:HGNC Symbol;Acc:HGNC:5002]","synonyms":"BRAF25,SOXL,SMARCE1r,HMGXB2,HMGX2,BRAF35","biotype":"protein_coding","ncbi_id":"10362","summary":null,"start":3572777,"end":3579088,"strand":1,"description":"high mobility group 20B [Source:HGNC Symbol;Acc:HGNC:5002]"}, {"versioned_ensembl_gene_id":"ENSG00000169164.7","gene_symbol":"AL159987.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55654709,"end":55657014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272053.1","gene_symbol":"AL160400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25014952,"end":25042170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232954.2","gene_symbol":"LINC00374","gene_name":"long intergenic non-protein coding RNA 374 [Source:HGNC Symbol;Acc:HGNC:42698]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144531","summary":null,"start":58211697,"end":58233117,"strand":-1,"description":"long intergenic non-protein coding RNA 374 [Source:HGNC Symbol;Acc:HGNC:42698]"}, {"versioned_ensembl_gene_id":"ENSG00000099624.7","gene_symbol":"ATP5D","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit [Source:HGNC Symbol;Acc:HGNC:837]","synonyms":null,"biotype":"protein_coding","ncbi_id":"513","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the delta subunit of the catalytic core. Alternatively spliced transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008]","start":1241746,"end":1244826,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit [Source:HGNC Symbol;Acc:HGNC:837]"}, {"versioned_ensembl_gene_id":"ENSG00000182783.5","gene_symbol":"OR2T29","gene_name":"olfactory receptor family 2 subfamily T member 29 [Source:HGNC Symbol;Acc:HGNC:31253]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343563","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248556912,"end":248562772,"strand":-1,"description":"olfactory receptor family 2 subfamily T member 29 [Source:HGNC Symbol;Acc:HGNC:31253]"}, {"versioned_ensembl_gene_id":"ENSG00000243149.1","gene_symbol":"LINC02040","gene_name":"long intergenic non-protein coding RNA 2040 [Source:HGNC Symbol;Acc:HGNC:52880]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724763","summary":null,"start":65174958,"end":65193499,"strand":1,"description":"long intergenic non-protein coding RNA 2040 [Source:HGNC Symbol;Acc:HGNC:52880]"}, {"versioned_ensembl_gene_id":"ENSG00000264006.6","gene_symbol":"AKR1C8P","gene_name":"aldo-keto reductase family 1 member C8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23469]","synonyms":"AKR1CL1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"340811","summary":null,"start":5154143,"end":5185187,"strand":-1,"description":"aldo-keto reductase family 1 member C8, pseudogene [Source:HGNC Symbol;Acc:HGNC:23469]"}, {"versioned_ensembl_gene_id":"ENSG00000224127.1","gene_symbol":"AC099786.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75127830,"end":75133058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233008.5","gene_symbol":"LINC01725","gene_name":"long intergenic non-protein coding RNA 1725 [Source:HGNC Symbol;Acc:HGNC:52513]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927587","summary":null,"start":83575776,"end":83861023,"strand":-1,"description":"long intergenic non-protein coding RNA 1725 [Source:HGNC Symbol;Acc:HGNC:52513]"}, {"versioned_ensembl_gene_id":"ENSG00000128595.16","gene_symbol":"CALU","gene_name":"calumenin [Source:HGNC Symbol;Acc:HGNC:1458]","synonyms":null,"biotype":"protein_coding","ncbi_id":"813","summary":"The product of this gene is a calcium-binding protein localized in the endoplasmic reticulum (ER) and it is involved in such ER functions as protein folding and sorting. This protein belongs to a family of multiple EF-hand proteins (CERC) that include reticulocalbin, ERC-55, and Cab45 and the product of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]","start":128739292,"end":128771807,"strand":1,"description":"calumenin [Source:HGNC Symbol;Acc:HGNC:1458]"}, {"versioned_ensembl_gene_id":"ENSG00000142230.11","gene_symbol":"SAE1","gene_name":"SUMO1 activating enzyme subunit 1 [Source:HGNC Symbol;Acc:HGNC:30660]","synonyms":"Sua1,FLJ3091,AOS1","biotype":"protein_coding","ncbi_id":"10055","summary":"Posttranslational modification of proteins by the addition of the small protein SUMO (see SUMO1; MIM 601912), or sumoylation, regulates protein structure and intracellular localization. SAE1 and UBA2 (MIM 613295) form a heterodimer that functions as a SUMO-activating enzyme for the sumoylation of proteins (Okuma et al., 1999 [PubMed 9920803]).[supplied by OMIM, Mar 2010]","start":47113274,"end":47210636,"strand":1,"description":"SUMO1 activating enzyme subunit 1 [Source:HGNC Symbol;Acc:HGNC:30660]"}, {"versioned_ensembl_gene_id":"ENSG00000229943.1","gene_symbol":"AC133865.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74963314,"end":74965118,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282312.1","gene_symbol":"IGHVII-51-2","gene_name":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]","synonyms":"IGHV(II)-51-2","biotype":"IG_V_pseudogene","ncbi_id":"28363","summary":null,"start":106609399,"end":106609657,"strand":-1,"description":"immunoglobulin heavy variable (II)-51-2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5684]"}, {"versioned_ensembl_gene_id":"ENSG00000261671.1","gene_symbol":"AL158211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22257786,"end":22258548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276761.2","gene_symbol":"CWC25","gene_name":"CWC25 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:25989]","synonyms":"FLJ20291,CCDC49","biotype":"protein_coding","ncbi_id":"54883","summary":"This gene encodes a factor that is part of the multi-protein C complex involved in pre-mRNA splicing. Alternatively spliced transcripts have been described for this gene. [provided by RefSeq, Nov 2012]","start":38601221,"end":38626268,"strand":-1,"description":"CWC25 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:25989]"}, {"versioned_ensembl_gene_id":"ENSG00000222012.1","gene_symbol":"AC005481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157614023,"end":157618765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243596.1","gene_symbol":"AC130509.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":146342996,"end":146348480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229493.9","gene_symbol":"HLA-DQB2","gene_name":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]","synonyms":"HLA-DXB","biotype":"protein_coding","ncbi_id":"3120","summary":"HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010]","start":32909857,"end":32917296,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 2 [Source:HGNC Symbol;Acc:HGNC:4945]"}, {"versioned_ensembl_gene_id":"ENSG00000226891.7","gene_symbol":"LINC01359","gene_name":"long intergenic non-protein coding RNA 1359 [Source:HGNC Symbol;Acc:HGNC:50591]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101927084","summary":null,"start":64972225,"end":65002489,"strand":-1,"description":"long intergenic non-protein coding RNA 1359 [Source:HGNC Symbol;Acc:HGNC:50591]"}, {"versioned_ensembl_gene_id":"ENSG00000258408.1","gene_symbol":"NT5CP2","gene_name":"5',3'-nucleotidase, cytosolic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20047]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"326611","summary":null,"start":73539221,"end":73539781,"strand":-1,"description":"5',3'-nucleotidase, cytosolic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20047]"}, {"versioned_ensembl_gene_id":"ENSG00000225418.1","gene_symbol":"AKR1C5P","gene_name":"aldo-keto reductase family 1 member C5, pseudogene [Source:HGNC Symbol;Acc:HGNC:44679]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996684","summary":null,"start":5122087,"end":5135226,"strand":-1,"description":"aldo-keto reductase family 1 member C5, pseudogene [Source:HGNC Symbol;Acc:HGNC:44679]"}, {"versioned_ensembl_gene_id":"ENSG00000249755.2","gene_symbol":"AC083829.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88527160,"end":88528170,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267459.1","gene_symbol":"AC006116.7","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":56377037,"end":56377792,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251350.1","gene_symbol":"LINC02475","gene_name":"long intergenic non-protein coding RNA 2475 [Source:HGNC Symbol;Acc:HGNC:53418]","synonyms":"LVCAT1","biotype":"lincRNA","ncbi_id":"100506827","summary":null,"start":44016861,"end":44022063,"strand":1,"description":"long intergenic non-protein coding RNA 2475 [Source:HGNC Symbol;Acc:HGNC:53418]"}, {"versioned_ensembl_gene_id":"ENSG00000273805.1","gene_symbol":"AC083805.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57894232,"end":57896846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179542.15","gene_symbol":"SLITRK4","gene_name":"SLIT and NTRK like family member 4 [Source:HGNC Symbol;Acc:HGNC:23502]","synonyms":"DKFZp547M2010","biotype":"protein_coding","ncbi_id":"139065","summary":"This gene encodes a transmembrane protein belonging to the the SLITRK family. These family members include two N-terminal leucine-rich repeat domains similar to those found in the axonal growth-controlling protein SLIT, as well as C-terminal regions similar to neurotrophin receptors. Studies of an homologous protein in mouse suggest that this family member functions to suppress neurite outgrowth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":143622790,"end":143635777,"strand":-1,"description":"SLIT and NTRK like family member 4 [Source:HGNC Symbol;Acc:HGNC:23502]"}, {"versioned_ensembl_gene_id":"ENSG00000241566.1","gene_symbol":"IGKV2D-24","gene_name":"immunoglobulin kappa variable 2D-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5797]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28885","summary":null,"start":90004797,"end":90005629,"strand":1,"description":"immunoglobulin kappa variable 2D-24 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5797]"}, {"versioned_ensembl_gene_id":"ENSG00000233191.1","gene_symbol":"AC006372.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":157513294,"end":157516841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280266.1","gene_symbol":"AC006372.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":157525783,"end":157527325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260133.1","gene_symbol":"CA5AP1","gene_name":"carbonic anhydrase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1379]","synonyms":"CA5P","biotype":"unprocessed_pseudogene","ncbi_id":"764","summary":null,"start":29618785,"end":29636328,"strand":-1,"description":"carbonic anhydrase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1379]"}, {"versioned_ensembl_gene_id":"ENSG00000234210.1","gene_symbol":"AC006372.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157466231,"end":157499716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223872.1","gene_symbol":"AC006372.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":157501322,"end":157503577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206490.11","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"ABC50,EST123147","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30560870,"end":30586674,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000229587.2","gene_symbol":"AL158825.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75009828,"end":75016036,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225398.3","gene_symbol":"PGM5P4","gene_name":"phosphoglucomutase 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49605]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729468","summary":null,"start":113541937,"end":113563298,"strand":1,"description":"phosphoglucomutase 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49605]"}, {"versioned_ensembl_gene_id":"ENSG00000272472.1","gene_symbol":"AL512283.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":122643388,"end":122644771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218502.3","gene_symbol":"H2AFZP3","gene_name":"H2A histone family member Z pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728023","summary":null,"start":99215372,"end":99215758,"strand":-1,"description":"H2A histone family member Z pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:38013]"}, {"versioned_ensembl_gene_id":"ENSG00000197213.9","gene_symbol":"ZSCAN5B","gene_name":"zinc finger and SCAN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:34246]","synonyms":"ZNF495B,ZNF371","biotype":"protein_coding","ncbi_id":"342933","summary":null,"start":56189570,"end":56197920,"strand":-1,"description":"zinc finger and SCAN domain containing 5B [Source:HGNC Symbol;Acc:HGNC:34246]"}, {"versioned_ensembl_gene_id":"ENSG00000175143.4","gene_symbol":"OR2T1","gene_name":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]","synonyms":"OR1-25","biotype":"protein_coding","ncbi_id":"26696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248403048,"end":248408020,"strand":1,"description":"olfactory receptor family 2 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:8277]"}, {"versioned_ensembl_gene_id":"ENSG00000117616.17","gene_symbol":"RSRP1","gene_name":"arginine and serine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:25234]","synonyms":"DJ465N24.2.1,C1orf63","biotype":"protein_coding","ncbi_id":"57035","summary":null,"start":25242237,"end":25338213,"strand":-1,"description":"arginine and serine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:25234]"}, {"versioned_ensembl_gene_id":"ENSG00000196944.4","gene_symbol":"OR2T4","gene_name":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]","synonyms":"OR2T4Q","biotype":"protein_coding","ncbi_id":"127074","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248361581,"end":248362627,"strand":1,"description":"olfactory receptor family 2 subfamily T member 4 [Source:HGNC Symbol;Acc:HGNC:15016]"}, {"versioned_ensembl_gene_id":"ENSG00000282013.1","gene_symbol":"RPH3AL","gene_name":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]","synonyms":"Noc2","biotype":"protein_coding","ncbi_id":"9501","summary":"The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]","start":281768,"end":388309,"strand":-1,"description":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]"}, {"versioned_ensembl_gene_id":"ENSG00000135549.14","gene_symbol":"PKIB","gene_name":"cAMP-dependent protein kinase inhibitor beta [Source:HGNC Symbol;Acc:HGNC:9018]","synonyms":"PRKACN2","biotype":"protein_coding","ncbi_id":"5570","summary":"This gene encodes a member of the cAMP-dependent protein kinase inhibitor family. The encoded protein may play a role in the protein kinase A (PKA) pathway by interacting with the catalytic subunit of PKA, and overexpression of this gene may play a role in prostate cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":122471917,"end":122726373,"strand":1,"description":"cAMP-dependent protein kinase inhibitor beta [Source:HGNC Symbol;Acc:HGNC:9018]"}, {"versioned_ensembl_gene_id":"ENSG00000131558.14","gene_symbol":"EXOC4","gene_name":"exocyst complex component 4 [Source:HGNC Symbol;Acc:HGNC:30389]","synonyms":"Sec8p,SEC8L1,SEC8,MGC27170,KIAA1699","biotype":"protein_coding","ncbi_id":"60412","summary":"The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":133253073,"end":134066589,"strand":1,"description":"exocyst complex component 4 [Source:HGNC Symbol;Acc:HGNC:30389]"}, {"versioned_ensembl_gene_id":"ENSG00000142409.5","gene_symbol":"ZNF787","gene_name":"zinc finger protein 787 [Source:HGNC Symbol;Acc:HGNC:26998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126208","summary":null,"start":56087366,"end":56121280,"strand":-1,"description":"zinc finger protein 787 [Source:HGNC Symbol;Acc:HGNC:26998]"}, {"versioned_ensembl_gene_id":"ENSG00000273655.1","gene_symbol":"AC012314.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54209707,"end":54210033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121753.12","gene_symbol":"ADGRB2","gene_name":"adhesion G protein-coupled receptor B2 [Source:HGNC Symbol;Acc:HGNC:944]","synonyms":"BAI2","biotype":"protein_coding","ncbi_id":"576","summary":"This gene encodes a a seven-span transmembrane protein that is thought to be a member of the secretin receptor family. The encoded protein is a brain-specific inhibitor of angiogenesis. The mature peptide may be further cleaved into additional products (PMID:20367554). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":31727117,"end":31764893,"strand":-1,"description":"adhesion G protein-coupled receptor B2 [Source:HGNC Symbol;Acc:HGNC:944]"}, {"versioned_ensembl_gene_id":"ENSG00000104324.15","gene_symbol":"CPQ","gene_name":"carboxypeptidase Q [Source:HGNC Symbol;Acc:HGNC:16910]","synonyms":"PGCP,LDP","biotype":"protein_coding","ncbi_id":"10404","summary":"This gene encodes a metallopeptidase that belongs to the peptidase M28 family. The encoded protein may catalyze the cleavage of dipeptides with unsubstituted terminals into amino acids. [provided by RefSeq, Jul 2013]","start":96645227,"end":97149654,"strand":1,"description":"carboxypeptidase Q [Source:HGNC Symbol;Acc:HGNC:16910]"}, {"versioned_ensembl_gene_id":"ENSG00000196741.5","gene_symbol":"LINC01560","gene_name":"long intergenic non-protein coding RNA 1560 [Source:HGNC Symbol;Acc:HGNC:27333]","synonyms":"CXorf24","biotype":"lincRNA","ncbi_id":"203414","summary":null,"start":47483571,"end":47484823,"strand":1,"description":"long intergenic non-protein coding RNA 1560 [Source:HGNC Symbol;Acc:HGNC:27333]"}, {"versioned_ensembl_gene_id":"ENSG00000148468.16","gene_symbol":"FAM171A1","gene_name":"family with sequence similarity 171 member A1 [Source:HGNC Symbol;Acc:HGNC:23522]","synonyms":"FLJ12884,C10orf38","biotype":"protein_coding","ncbi_id":"221061","summary":null,"start":15211643,"end":15371062,"strand":-1,"description":"family with sequence similarity 171 member A1 [Source:HGNC Symbol;Acc:HGNC:23522]"}, {"versioned_ensembl_gene_id":"ENSG00000267779.5","gene_symbol":"LINC01533","gene_name":"long intergenic non-protein coding RNA 1533 [Source:HGNC Symbol;Acc:HGNC:51274]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996665","summary":null,"start":32025862,"end":32056865,"strand":1,"description":"long intergenic non-protein coding RNA 1533 [Source:HGNC Symbol;Acc:HGNC:51274]"}, {"versioned_ensembl_gene_id":"ENSG00000228900.1","gene_symbol":"BX927182.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745361,"end":29745585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273558.1","gene_symbol":"AL512310.11","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19637225,"end":19641306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269246.1","gene_symbol":"AC011445.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39341773,"end":39341945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213853.9","gene_symbol":"EMP2","gene_name":"epithelial membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:3334]","synonyms":"XMP","biotype":"protein_coding","ncbi_id":"2013","summary":"This gene encodes a tetraspan protein of the PMP22/EMP family. The encoded protein regulates cell membrane composition. It has been associated with various functions including endocytosis, cell signaling, cell proliferation, cell migration, cell adhesion, cell death, cholesterol homeostasis, urinary albumin excretion, and embryo implantation. It is known to negatively regulate caveolin-1, a scaffolding protein which is the main component of the caveolae plasma membrane invaginations found in most cell types. Through activation of PTK2 it positively regulates vascular endothelial growth factor A. It also modulates the function of specific integrin isomers in the plasma membrane. Up-regulation of this gene has been linked to cancer progression in multiple different tissues. Mutations in this gene have been associated with nephrotic syndrome type 10 (NPHS10). [provided by RefSeq, Mar 2015]","start":10528422,"end":10580698,"strand":-1,"description":"epithelial membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:3334]"}, {"versioned_ensembl_gene_id":"ENSG00000278184.1","gene_symbol":"NF1P11","gene_name":"neurofibromin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51738]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106481736","summary":null,"start":19612191,"end":19619490,"strand":1,"description":"neurofibromin 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51738]"}, {"versioned_ensembl_gene_id":"ENSG00000149925.17","gene_symbol":"ALDOA","gene_name":"aldolase, fructose-bisphosphate A [Source:HGNC Symbol;Acc:HGNC:414]","synonyms":null,"biotype":"protein_coding","ncbi_id":"226","summary":"This gene encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10. [provided by RefSeq, Sep 2017]","start":30053090,"end":30070457,"strand":1,"description":"aldolase, fructose-bisphosphate A [Source:HGNC Symbol;Acc:HGNC:414]"}, {"versioned_ensembl_gene_id":"ENSG00000229099.1","gene_symbol":"CR933540.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32679833,"end":32698994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281031.1","gene_symbol":"IGLV3-30","gene_name":"immunoglobulin lambda variable 3-30 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5912]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28789","summary":null,"start":22627677,"end":22628268,"strand":1,"description":"immunoglobulin lambda variable 3-30 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5912]"}, {"versioned_ensembl_gene_id":"ENSG00000229104.1","gene_symbol":"YY1P2","gene_name":"YY1 transcription factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45095]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647012","summary":null,"start":138897151,"end":138898098,"strand":1,"description":"YY1 transcription factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45095]"}, {"versioned_ensembl_gene_id":"ENSG00000256424.1","gene_symbol":"LINC02414","gene_name":"long intergenic non-protein coding RNA 2414 [Source:HGNC Symbol;Acc:HGNC:53343]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370085","summary":null,"start":131647113,"end":131648121,"strand":-1,"description":"long intergenic non-protein coding RNA 2414 [Source:HGNC Symbol;Acc:HGNC:53343]"}, {"versioned_ensembl_gene_id":"ENSG00000278432.1","gene_symbol":"AC245128.16","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260059.1","gene_symbol":"AC092620.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138599663,"end":138602426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251178.1","gene_symbol":"AC083906.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130034553,"end":130035539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273362.1","gene_symbol":"AP000547.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16521059,"end":16527237,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261679.2","gene_symbol":"AC009852.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43267904,"end":43268388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259681.1","gene_symbol":"AC090527.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45558598,"end":45562877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276731.1","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"CD158B1,nkat6,CD158k,cl-43","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754688,"end":54769216,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000179136.6","gene_symbol":"LINC00670","gene_name":"long intergenic non-protein coding RNA 670 [Source:HGNC Symbol;Acc:HGNC:44338]","synonyms":"FLJ34690","biotype":"lincRNA","ncbi_id":"284034","summary":null,"start":12549782,"end":12642854,"strand":1,"description":"long intergenic non-protein coding RNA 670 [Source:HGNC Symbol;Acc:HGNC:44338]"}, {"versioned_ensembl_gene_id":"ENSG00000267593.1","gene_symbol":"LINC01926","gene_name":"long intergenic non-protein coding RNA 1926 [Source:HGNC Symbol;Acc:HGNC:52748]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372147","summary":null,"start":58813880,"end":58834364,"strand":1,"description":"long intergenic non-protein coding RNA 1926 [Source:HGNC Symbol;Acc:HGNC:52748]"}, {"versioned_ensembl_gene_id":"ENSG00000232140.1","gene_symbol":"AC073257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120553743,"end":120558109,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280319.1","gene_symbol":"AC073578.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131436447,"end":131436960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255533.1","gene_symbol":"AC136475.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":303856,"end":304144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218806.2","gene_symbol":"AL133264.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24750671,"end":24751625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153767.9","gene_symbol":"GTF2E1","gene_name":"general transcription factor IIE subunit 1 [Source:HGNC Symbol;Acc:HGNC:4650]","synonyms":"FE,TFIIE-A","biotype":"protein_coding","ncbi_id":"2960","summary":null,"start":120742637,"end":120783069,"strand":1,"description":"general transcription factor IIE subunit 1 [Source:HGNC Symbol;Acc:HGNC:4650]"}, {"versioned_ensembl_gene_id":"ENSG00000223803.1","gene_symbol":"RPS20P14","gene_name":"ribosomal protein S20 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36692]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440992","summary":null,"start":186900198,"end":186900557,"strand":1,"description":"ribosomal protein S20 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36692]"}, {"versioned_ensembl_gene_id":"ENSG00000226482.1","gene_symbol":"ADIPOQ-AS1","gene_name":"ADIPOQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40648]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874095","summary":null,"start":186851886,"end":186856123,"strand":-1,"description":"ADIPOQ antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40648]"}, {"versioned_ensembl_gene_id":"ENSG00000235728.1","gene_symbol":"AC007349.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36781008,"end":36782789,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268262.1","gene_symbol":"AC011445.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":39314651,"end":39320858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282775.1","gene_symbol":"AC243829.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36072866,"end":36090134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204876.4","gene_symbol":"AC021218.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155962632,"end":155966343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264015.1","gene_symbol":"AC124254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77421619,"end":77560763,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264736.1","gene_symbol":"BDP1P","gene_name":"B double prime 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"724038","summary":null,"start":77435253,"end":77437242,"strand":-1,"description":"B double prime 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31044]"}, {"versioned_ensembl_gene_id":"ENSG00000106554.12","gene_symbol":"CHCHD3","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21906]","synonyms":"PPP1R22,MINOS3,Mic19,FLJ20420","biotype":"protein_coding","ncbi_id":"54927","summary":"The protein encoded by this gene is an inner mitochondrial membrane scaffold protein. Absence of the encoded protein affects the structural integrity of mitochondrial cristae and leads to reductions in ATP production, cell growth, and oxygen consumption. This protein is part of the mitochondrial contact site and cristae organizing system (MICOS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":132784868,"end":133082088,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 3 [Source:HGNC Symbol;Acc:HGNC:21906]"}, {"versioned_ensembl_gene_id":"ENSG00000281486.1","gene_symbol":"SNTG2","gene_name":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]","synonyms":"SYN5,G2SYN","biotype":"protein_coding","ncbi_id":"54221","summary":"This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq, Jul 2008]","start":1209102,"end":1269668,"strand":1,"description":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]"}, {"versioned_ensembl_gene_id":"ENSG00000274042.2","gene_symbol":"GOLGA6L10","gene_name":"golgin A6 family-like 10 [Source:NCBI gene;Acc:647042]","synonyms":"GOLGA6L18,GOLGA6L18","biotype":"protein_coding","ncbi_id":"647042","summary":null,"start":82342783,"end":82349497,"strand":-1,"description":"golgin A6 family-like 10 [Source:NCBI gene;Acc:647042]"}, {"versioned_ensembl_gene_id":"ENSG00000241749.4","gene_symbol":"RPSAP52","gene_name":"ribosomal protein SA pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:35752]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"204010","summary":null,"start":65758020,"end":65826997,"strand":-1,"description":"ribosomal protein SA pseudogene 52 [Source:HGNC Symbol;Acc:HGNC:35752]"}, {"versioned_ensembl_gene_id":"ENSG00000163737.3","gene_symbol":"PF4","gene_name":"platelet factor 4 [Source:HGNC Symbol;Acc:HGNC:8861]","synonyms":"SCYB4,CXCL4","biotype":"protein_coding","ncbi_id":"5196","summary":"This gene encodes a member of the CXC chemokine family. This chemokine is released from the alpha granules of activated platelets in the form of a homotetramer which has high affinity for heparin and is involved in platelet aggregation. This protein is chemotactic for numerous other cell type and also functions as an inhibitor of hematopoiesis, angiogenesis and T-cell function. The protein also exhibits antimicrobial activity against Plasmodium falciparum. [provided by RefSeq, Oct 2014]","start":73981077,"end":73982124,"strand":-1,"description":"platelet factor 4 [Source:HGNC Symbol;Acc:HGNC:8861]"}, {"versioned_ensembl_gene_id":"ENSG00000122145.14","gene_symbol":"TBX22","gene_name":"T-box 22 [Source:HGNC Symbol;Acc:HGNC:11600]","synonyms":"CPX,CLPA","biotype":"protein_coding","ncbi_id":"50945","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":80014756,"end":80031769,"strand":1,"description":"T-box 22 [Source:HGNC Symbol;Acc:HGNC:11600]"}, {"versioned_ensembl_gene_id":"ENSG00000131002.11","gene_symbol":"TXLNGY","gene_name":"taxilin gamma pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:18473]","synonyms":"TXLNG2P,CYorf15B,CYorf15A","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"246126","summary":null,"start":19567313,"end":19606274,"strand":1,"description":"taxilin gamma pseudogene, Y-linked [Source:HGNC Symbol;Acc:HGNC:18473]"}, {"versioned_ensembl_gene_id":"ENSG00000237419.1","gene_symbol":"AL954642.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":138199933,"end":138203325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259305.6","gene_symbol":"ZHX1-C8orf76","gene_name":"ZHX1-C8orf76 readthrough [Source:HGNC Symbol;Acc:HGNC:42975]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100533106","summary":"This locus represents naturally occurring read-through transcription between the neighboring zinc fingers and homeoboxes 1 (ZHX1) and chromosome 8 open reading frame 76 (C8orf76) genes. The read-through transcript encodes a protein that shares sequence identity with the downstream gene, but it has a distinct N-terminus encoded by exon structure from the upstream gene. [provided by RefSeq, Feb 2011]","start":123226189,"end":123274284,"strand":-1,"description":"ZHX1-C8orf76 readthrough [Source:HGNC Symbol;Acc:HGNC:42975]"}, {"versioned_ensembl_gene_id":"ENSG00000243498.2","gene_symbol":"AC068228.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123236852,"end":123237062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164305.18","gene_symbol":"CASP3","gene_name":"caspase 3 [Source:HGNC Symbol;Acc:HGNC:1504]","synonyms":"Yama,CPP32B,CPP32,apopain","biotype":"protein_coding","ncbi_id":"836","summary":"The protein encoded by this gene is a cysteine-aspartic acid protease that plays a central role in the execution-phase of cell apoptosis. The encoded protein cleaves and inactivates poly(ADP-ribose) polymerase while it cleaves and activates sterol regulatory element binding proteins as well as caspases 6, 7, and 9. This protein itself is processed by caspases 8, 9, and 10. It is the predominant caspase involved in the cleavage of amyloid-beta 4A precursor protein, which is associated with neuronal death in Alzheimer's disease. [provided by RefSeq, Aug 2017]","start":184627696,"end":184649509,"strand":-1,"description":"caspase 3 [Source:HGNC Symbol;Acc:HGNC:1504]"}, {"versioned_ensembl_gene_id":"ENSG00000225082.2","gene_symbol":"DAP3P1","gene_name":"death associated protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17624]","synonyms":"MRPS29P1,DAP3P","biotype":"unprocessed_pseudogene","ncbi_id":"359804","summary":null,"start":155586644,"end":155602197,"strand":1,"description":"death associated protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17624]"}, {"versioned_ensembl_gene_id":"ENSG00000259288.6","gene_symbol":"BUB1B-PAK6","gene_name":"BUB1B-PAK6 readthrough [Source:HGNC Symbol;Acc:HGNC:52276]","synonyms":null,"biotype":"protein_coding","ncbi_id":"106821730","summary":"This gene represents readthrough transcription between the genes BUB1B (mitotic checkpoint serine/threonine-protein kinase BUB1 beta) and PAK6 (serine/threonine-protein kinase PAK 6). The protein encoded by the readthrough transcripts is the same as the product of the downstream gene (PAK6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":40217428,"end":40276396,"strand":1,"description":"BUB1B-PAK6 readthrough [Source:HGNC Symbol;Acc:HGNC:52276]"}, {"versioned_ensembl_gene_id":"ENSG00000105409.16","gene_symbol":"ATP1A3","gene_name":"ATPase Na+/K+ transporting subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:801]","synonyms":"DYT12","biotype":"protein_coding","ncbi_id":"478","summary":"The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 3 subunit. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":41966582,"end":41997497,"strand":-1,"description":"ATPase Na+/K+ transporting subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:801]"}, {"versioned_ensembl_gene_id":"ENSG00000231035.1","gene_symbol":"RPL7L1P9","gene_name":"ribosomal protein L7 like 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39491]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128899","summary":null,"start":217760547,"end":217761291,"strand":-1,"description":"ribosomal protein L7 like 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39491]"}, {"versioned_ensembl_gene_id":"ENSG00000213015.8","gene_symbol":"ZNF580","gene_name":"zinc finger protein 580 [Source:HGNC Symbol;Acc:HGNC:29473]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51157","summary":null,"start":55635016,"end":55643469,"strand":1,"description":"zinc finger protein 580 [Source:HGNC Symbol;Acc:HGNC:29473]"}, {"versioned_ensembl_gene_id":"ENSG00000283549.1","gene_symbol":"AC007161.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7640752,"end":8004053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235539.1","gene_symbol":"MTND1P33","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42082]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873218","summary":null,"start":143433042,"end":143433958,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42082]"}, {"versioned_ensembl_gene_id":"ENSG00000229423.2","gene_symbol":"RPL27AP8","gene_name":"ribosomal protein L27a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36544]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271605","summary":null,"start":47766640,"end":47767085,"strand":-1,"description":"ribosomal protein L27a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36544]"}, {"versioned_ensembl_gene_id":"ENSG00000278086.1","gene_symbol":"GU182347.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54888943,"end":54903379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282277.1","gene_symbol":"CYP3A51P","gene_name":"cytochrome P450 family 3 subfamily A member 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:42418]","synonyms":"CYP3A5P1,CYP3A5-de1b2b,CYP3A5-de13c","biotype":"unprocessed_pseudogene","ncbi_id":"1578","summary":"This locus represents a CYP3A pseudogene that is present within a cluster of CYP3A (cytochrome P450, family 3, subfamily A) genes on chromosome 7. This pseudogene is located between the CYP3A7 and CYP3A5 family members. It contains duplicates of exons 1, 2 and 13 that are found in the functional genes. Readthrough transcription exists between the CYP3A7 gene and this pseudogene, where the readthrough transcript includes CYP3A7 exons 1-13 and exons 2 and 13 of this pseudogene, as represented in GeneID:100861540. This pseudogene is not known to be independently transcribed. [provided by RefSeq, Feb 2012]","start":99685145,"end":99700034,"strand":-1,"description":"cytochrome P450 family 3 subfamily A member 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:42418]"}, {"versioned_ensembl_gene_id":"ENSG00000260778.5","gene_symbol":"AC009065.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2268155,"end":2273418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228488.1","gene_symbol":"AC092168.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100722221,"end":100722882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239571.1","gene_symbol":"IGKV2D-30","gene_name":"immunoglobulin kappa variable 2D-30 [Source:HGNC Symbol;Acc:HGNC:5801]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28881","summary":null,"start":89936859,"end":89937679,"strand":1,"description":"immunoglobulin kappa variable 2D-30 [Source:HGNC Symbol;Acc:HGNC:5801]"}, {"versioned_ensembl_gene_id":"ENSG00000261012.2","gene_symbol":"AC115619.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20999313,"end":21000917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225210.9","gene_symbol":"DUXAP9","gene_name":"double homeobox A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:32188]","synonyms":"LINC01296,FLJ39632","biotype":"transcribed_processed_pseudogene","ncbi_id":"503638","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":19062316,"end":19115270,"strand":1,"description":"double homeobox A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:32188]"}, {"versioned_ensembl_gene_id":"ENSG00000271140.1","gene_symbol":"PRR20FP","gene_name":"proline rich 20F, pseudogene [Source:HGNC Symbol;Acc:HGNC:49097]","synonyms":"PRR20F","biotype":"unprocessed_pseudogene","ncbi_id":"106480416","summary":null,"start":57173453,"end":57173632,"strand":1,"description":"proline rich 20F, pseudogene [Source:HGNC Symbol;Acc:HGNC:49097]"}, {"versioned_ensembl_gene_id":"ENSG00000165905.17","gene_symbol":"LARGE2","gene_name":"LARGE xylosyl- and glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16522]","synonyms":"PP5656,GYLTL1B,FLJ35207","biotype":"protein_coding","ncbi_id":"120071","summary":null,"start":45921621,"end":45929096,"strand":1,"description":"LARGE xylosyl- and glucuronyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:16522]"}, {"versioned_ensembl_gene_id":"ENSG00000251354.3","gene_symbol":"AC024451.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":47546804,"end":47547926,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205846.3","gene_symbol":"CLEC6A","gene_name":"C-type lectin domain containing 6A [Source:HGNC Symbol;Acc:HGNC:14556]","synonyms":"dectin-2,CLECSF10","biotype":"protein_coding","ncbi_id":"93978","summary":"The protein encoded by this gene is a type II membrane receptor with an extracellular C-type lectin-like domain fold. The extracellular portion binds structures with a high mannose content and has been shown to recognize several pathogens, including C. elegans, S. cerevisiae, M. tuberculosis, C. neoformans, and house dust mite. When stimulated, the encoded protein initiates signalling through the CARD9-Bcl10-Malt1 pathway, leading to the induction of cytokines. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":8455926,"end":8478330,"strand":1,"description":"C-type lectin domain containing 6A [Source:HGNC Symbol;Acc:HGNC:14556]"}, {"versioned_ensembl_gene_id":"ENSG00000232369.1","gene_symbol":"AL136380.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44988234,"end":44988725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236297.1","gene_symbol":"AC048351.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":193578812,"end":193593090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231523.1","gene_symbol":"SEPT14P1","gene_name":"septin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51685]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480340","summary":null,"start":63117501,"end":63154934,"strand":-1,"description":"septin 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51685]"}, {"versioned_ensembl_gene_id":"ENSG00000257335.8","gene_symbol":"MGAM","gene_name":"maltase-glucoamylase [Source:HGNC Symbol;Acc:HGNC:7043]","synonyms":"MGA","biotype":"protein_coding","ncbi_id":"8972","summary":"This gene encodes maltase-glucoamylase, which is a brush border membrane enzyme that plays a role in the final steps of digestion of starch. The protein has two catalytic sites identical to those of sucrase-isomaltase, but the proteins are only 59% homologous. Both are members of glycosyl hydrolase family 31, which has a variety of substrate specificities. [provided by RefSeq, Jul 2008]","start":141907813,"end":142106747,"strand":1,"description":"maltase-glucoamylase [Source:HGNC Symbol;Acc:HGNC:7043]"}, {"versioned_ensembl_gene_id":"ENSG00000160688.18","gene_symbol":"FLAD1","gene_name":"flavin adenine dinucleotide synthetase 1 [Source:HGNC Symbol;Acc:HGNC:24671]","synonyms":"PP591,FAD1","biotype":"protein_coding","ncbi_id":"80308","summary":"This gene encodes the enzyme that catalyzes adenylation of flavin mononucleotide (FMN) to form flavin adenine dinucleotide (FAD) coenzyme. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":154983338,"end":154993111,"strand":1,"description":"flavin adenine dinucleotide synthetase 1 [Source:HGNC Symbol;Acc:HGNC:24671]"}, {"versioned_ensembl_gene_id":"ENSG00000206457.10","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"C6orf18,HCR","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31134861,"end":31150652,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000273780.2","gene_symbol":"ARHGAP23","gene_name":"Rho GTPase activating protein 23 [Source:HGNC Symbol;Acc:HGNC:29293]","synonyms":"KIAA1501","biotype":"protein_coding","ncbi_id":"57636","summary":"The RHO (see ARHA; MIM 165390) family of small GTPases are involved in signal transduction through transmembrane receptors, and they are inactive in the GDP-bound form and active in the GTP-bound form. GTPase-activating proteins, such as ARHGAP23, inactivate RHO family proteins by stimulating their hydrolysis of GTP (Katoh and Katoh, 2004 [PubMed 15254754]).[supplied by OMIM, Mar 2008]","start":38229196,"end":38313162,"strand":1,"description":"Rho GTPase activating protein 23 [Source:HGNC Symbol;Acc:HGNC:29293]"}, {"versioned_ensembl_gene_id":"ENSG00000234312.1","gene_symbol":"SAPCD2P4","gene_name":"suppressor APC domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442318","summary":null,"start":63113635,"end":63114805,"strand":-1,"description":"suppressor APC domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51280]"}, {"versioned_ensembl_gene_id":"ENSG00000223874.1","gene_symbol":"LINC01921","gene_name":"long intergenic non-protein coding RNA 1921 [Source:HGNC Symbol;Acc:HGNC:52740]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928327","summary":null,"start":216870772,"end":216871639,"strand":1,"description":"long intergenic non-protein coding RNA 1921 [Source:HGNC Symbol;Acc:HGNC:52740]"}, {"versioned_ensembl_gene_id":"ENSG00000225469.3","gene_symbol":"AL023773.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":142172866,"end":142173989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124875.9","gene_symbol":"CXCL6","gene_name":"C-X-C motif chemokine ligand 6 [Source:HGNC Symbol;Acc:HGNC:10643]","synonyms":"SCYB6,GCP-2,CKA-3","biotype":"protein_coding","ncbi_id":"6372","summary":"The protein encoded by this gene is a member CXC chemokine family. The encoded protein is a chemotactic for neutrophil granulocytes and has antibacterial action against gram-negative and gram-positive bacteria. This gene and other members of the CXC chemokine gene family form a gene cluster in a region of chromosome 4q. [provided by RefSeq, Jun 2020]","start":73836497,"end":73849064,"strand":1,"description":"C-X-C motif chemokine ligand 6 [Source:HGNC Symbol;Acc:HGNC:10643]"}, {"versioned_ensembl_gene_id":"ENSG00000229568.1","gene_symbol":"SMC4P1","gene_name":"structural maintenance of chromosomes 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51919]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421125","summary":null,"start":136544712,"end":136545542,"strand":1,"description":"structural maintenance of chromosomes 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51919]"}, {"versioned_ensembl_gene_id":"ENSG00000235843.1","gene_symbol":"AL390961.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26717635,"end":26718778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162086.14","gene_symbol":"ZNF75A","gene_name":"zinc finger protein 75a [Source:HGNC Symbol;Acc:HGNC:13146]","synonyms":"FLJ31529","biotype":"protein_coding","ncbi_id":"7627","summary":null,"start":3305406,"end":3318852,"strand":1,"description":"zinc finger protein 75a [Source:HGNC Symbol;Acc:HGNC:13146]"}, {"versioned_ensembl_gene_id":"ENSG00000227347.1","gene_symbol":"HNRNPKP2","gene_name":"heterogeneous nuclear ribonucleoprotein K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42375]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389053","summary":null,"start":136199114,"end":136200503,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein K pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42375]"}, {"versioned_ensembl_gene_id":"ENSG00000231370.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"D6S51E,BAT2,G2","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31602891,"end":31619942,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000225031.1","gene_symbol":"EIF4BP7","gene_name":"eukaryotic translation initiation factor 4B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643873","summary":null,"start":111619677,"end":111621489,"strand":-1,"description":"eukaryotic translation initiation factor 4B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37940]"}, {"versioned_ensembl_gene_id":"ENSG00000224230.1","gene_symbol":"BX927235.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32555366,"end":32555461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279840.1","gene_symbol":"AC004801.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47960497,"end":47963469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162585.16","gene_symbol":"FAAP20","gene_name":"Fanconi anemia core complex associated protein 20 [Source:HGNC Symbol;Acc:HGNC:26428]","synonyms":"FLJ31031,C1orf86","biotype":"protein_coding","ncbi_id":"199990","summary":null,"start":2184461,"end":2212720,"strand":-1,"description":"Fanconi anemia core complex associated protein 20 [Source:HGNC Symbol;Acc:HGNC:26428]"}, {"versioned_ensembl_gene_id":"ENSG00000237963.1","gene_symbol":"AL441964.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65356890,"end":65357547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072952.18","gene_symbol":"MRVI1","gene_name":"murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:HGNC:7237]","synonyms":"JAW1L,IRAG","biotype":"protein_coding","ncbi_id":"10335","summary":"This gene is similar to a putative mouse tumor suppressor gene (Mrvi1) that is frequently disrupted by mouse AIDS-related virus (MRV). The encoded protein, which is found in the membrane of the endoplasmic reticulum, is similar to Jaw1, a lymphoid-restricted protein whose expression is down-regulated during lymphoid differentiation. This protein is a substrate of cGMP-dependent kinase-1 (PKG1) that can function as a regulator of IP3-induced calcium release. Studies in mouse suggest that MRV integration at Mrvi1 induces myeloid leukemia by altering the expression of a gene important for myeloid cell growth and/or differentiation, and thus this gene may function as a myeloid leukemia tumor suppressor gene. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, and alternative translation start sites, including a non-AUG (CUG) start site, are used. [provided by RefSeq, May 2011]","start":10573091,"end":10693988,"strand":-1,"description":"murine retrovirus integration site 1 homolog [Source:HGNC Symbol;Acc:HGNC:7237]"}, {"versioned_ensembl_gene_id":"ENSG00000227521.2","gene_symbol":"AL390840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94319038,"end":94320025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261248.1","gene_symbol":"AC009120.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74282415,"end":74287519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229080.1","gene_symbol":"MTCO3P30","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52133]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075229","summary":null,"start":31505946,"end":31506615,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:52133]"}, {"versioned_ensembl_gene_id":"ENSG00000257494.1","gene_symbol":"AC004217.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112256800,"end":112259091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234322.1","gene_symbol":"ST13P18","gene_name":"ST13, Hsp70 interacting protein pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38861]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643310","summary":null,"start":93287733,"end":93288759,"strand":-1,"description":"ST13, Hsp70 interacting protein pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38861]"}, {"versioned_ensembl_gene_id":"ENSG00000239255.1","gene_symbol":"AC007620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179452395,"end":179452419,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225974.1","gene_symbol":"AC005550.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15689075,"end":15690854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229108.1","gene_symbol":"MEOX2-AS1","gene_name":"MEOX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50672]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927524","summary":null,"start":15688378,"end":15695491,"strand":1,"description":"MEOX2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50672]"}, {"versioned_ensembl_gene_id":"ENSG00000282286.1","gene_symbol":"IGHV3-13","gene_name":"immunoglobulin heavy variable 3-13 [Source:HGNC Symbol;Acc:HGNC:5581]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28449","summary":null,"start":106130311,"end":106130843,"strand":-1,"description":"immunoglobulin heavy variable 3-13 [Source:HGNC Symbol;Acc:HGNC:5581]"}, {"versioned_ensembl_gene_id":"ENSG00000228695.10","gene_symbol":"CES1P1","gene_name":"carboxylesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18546]","synonyms":"PCE-3,CESR,CES4,CES1A3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"51716","summary":"This gene is a member of the carboxylesterase (CES) gene family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene does not encode a protein and the sequence is similar to the CES1 gene, so represents a pseudogene of the CES1 gene. [provided by RefSeq, Jun 2010]","start":55760566,"end":55793960,"strand":1,"description":"carboxylesterase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18546]"}, {"versioned_ensembl_gene_id":"ENSG00000128567.16","gene_symbol":"PODXL","gene_name":"podocalyxin like [Source:HGNC Symbol;Acc:HGNC:9171]","synonyms":"PCLP,PC,Gp200","biotype":"protein_coding","ncbi_id":"5420","summary":"This gene encodes a member of the sialomucin protein family. The encoded protein was originally identified as an important component of glomerular podocytes. Podocytes are highly differentiated epithelial cells with interdigitating foot processes covering the outer aspect of the glomerular basement membrane. Other biological activities of the encoded protein include: binding in a membrane protein complex with Na+/H+ exchanger regulatory factor to intracellular cytoskeletal elements, playing a role in hematopoetic cell differentiation, and being expressed in vascular endothelium cells and binding to L-selectin. [provided by RefSeq, Jul 2008]","start":131500262,"end":131558217,"strand":-1,"description":"podocalyxin like [Source:HGNC Symbol;Acc:HGNC:9171]"}, {"versioned_ensembl_gene_id":"ENSG00000213676.10","gene_symbol":"ATF6B","gene_name":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]","synonyms":"G13,CREBL1","biotype":"protein_coding","ncbi_id":"1388","summary":"The protein encoded by this gene is a transcription factor in the unfolded protein response (UPR) pathway during ER stress. Either as a homodimer or as a heterodimer with ATF6-alpha, the encoded protein binds to the ER stress response element, interacting with nuclear transcription factor Y to activate UPR target genes. The protein is normally found in the membrane of the endoplasmic reticulum; however, under ER stress, the N-terminal cytoplasmic domain is cleaved from the rest of the protein and translocates to the nucleus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":32098176,"end":32128253,"strand":-1,"description":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]"}, {"versioned_ensembl_gene_id":"ENSG00000250423.2","gene_symbol":"KIAA1210","gene_name":"KIAA1210 [Source:HGNC Symbol;Acc:HGNC:29218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57481","summary":null,"start":119078635,"end":119150579,"strand":-1,"description":"KIAA1210 [Source:HGNC Symbol;Acc:HGNC:29218]"}, {"versioned_ensembl_gene_id":"ENSG00000171016.11","gene_symbol":"PYGO1","gene_name":"pygopus family PHD finger 1 [Source:HGNC Symbol;Acc:HGNC:30256]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26108","summary":null,"start":55538890,"end":55588947,"strand":-1,"description":"pygopus family PHD finger 1 [Source:HGNC Symbol;Acc:HGNC:30256]"}, {"versioned_ensembl_gene_id":"ENSG00000260399.1","gene_symbol":"AC100756.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23337985,"end":23341848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237070.1","gene_symbol":"AC005550.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15667947,"end":15681980,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260765.2","gene_symbol":"CES1P2","gene_name":"carboxylesterase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48928]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"390732","summary":null,"start":55728115,"end":55750111,"strand":1,"description":"carboxylesterase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48928]"}, {"versioned_ensembl_gene_id":"ENSG00000213265.8","gene_symbol":"TSGA13","gene_name":"testis specific 13 [Source:HGNC Symbol;Acc:HGNC:12369]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114960","summary":null,"start":130668648,"end":130687432,"strand":-1,"description":"testis specific 13 [Source:HGNC Symbol;Acc:HGNC:12369]"}, {"versioned_ensembl_gene_id":"ENSG00000238135.1","gene_symbol":"USP9YP10","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38454]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421222","summary":null,"start":18826107,"end":18829487,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38454]"}, {"versioned_ensembl_gene_id":"ENSG00000237873.1","gene_symbol":"AL158053.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93042490,"end":93042942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282366.1","gene_symbol":"IGHV1-12","gene_name":"immunoglobulin heavy variable 1-12 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5546]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28471","summary":null,"start":106123191,"end":106123480,"strand":-1,"description":"immunoglobulin heavy variable 1-12 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5546]"}, {"versioned_ensembl_gene_id":"ENSG00000230904.1","gene_symbol":"XKRYP2","gene_name":"XK related, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23909]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379029","summary":null,"start":18811338,"end":18811829,"strand":-1,"description":"XK related, Y-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23909]"}, {"versioned_ensembl_gene_id":"ENSG00000120519.14","gene_symbol":"SLC10A7","gene_name":"solute carrier family 10 member 7 [Source:HGNC Symbol;Acc:HGNC:23088]","synonyms":"MGC25043,DKFZp779O2438,DKFZp566M114,DKFZp313H0531,C4orf13","biotype":"protein_coding","ncbi_id":"84068","summary":null,"start":146253975,"end":146521964,"strand":-1,"description":"solute carrier family 10 member 7 [Source:HGNC Symbol;Acc:HGNC:23088]"}, {"versioned_ensembl_gene_id":"ENSG00000259433.2","gene_symbol":"AC051619.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45330209,"end":45332634,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274471.1","gene_symbol":"AC242376.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23309607,"end":23313276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280341.1","gene_symbol":"AP000542.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15282557,"end":15288670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279837.1","gene_symbol":"AC112694.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18601882,"end":18602649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215864.5","gene_symbol":"NBPF7","gene_name":"NBPF member 7 [Source:HGNC Symbol;Acc:HGNC:31989]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"343505","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Mar 2013]","start":119834870,"end":119844514,"strand":-1,"description":"NBPF member 7 [Source:HGNC Symbol;Acc:HGNC:31989]"}, {"versioned_ensembl_gene_id":"ENSG00000230097.2","gene_symbol":"ME2P1","gene_name":"malic enzyme 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49809]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286239","summary":null,"start":29824742,"end":29826711,"strand":-1,"description":"malic enzyme 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49809]"}, {"versioned_ensembl_gene_id":"ENSG00000274099.1","gene_symbol":"ABCB10P1","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]","synonyms":"ABCB10P2,ABCB10P,MABC2,M-ABC2","biotype":"processed_pseudogene","ncbi_id":"56476","summary":null,"start":23179869,"end":23182049,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]"}, {"versioned_ensembl_gene_id":"ENSG00000237155.3","gene_symbol":"IER3","gene_name":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]","synonyms":"IEX-1,PRG1,DIF-2,IEX-1L","biotype":"protein_coding","ncbi_id":"8870","summary":"This gene functions in the protection of cells from Fas- or tumor necrosis factor type alpha-induced apoptosis. Partially degraded and unspliced transcripts are found after virus infection in vitro, but these transcripts are not found in vivo and do not generate a valid protein. [provided by RefSeq, Jul 2008]","start":30733058,"end":30734413,"strand":-1,"description":"immediate early response 3 [Source:HGNC Symbol;Acc:HGNC:5392]"}, {"versioned_ensembl_gene_id":"ENSG00000250923.1","gene_symbol":"AC023141.12","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57773183,"end":57773381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237964.3","gene_symbol":"AC068042.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179399728,"end":179400875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228229.2","gene_symbol":"AC243961.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13324039,"end":13324518,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237700.2","gene_symbol":"PRAMEF33","gene_name":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]","synonyms":"PRAMEF33P,PRAMEF33P","biotype":"protein_coding","ncbi_id":"645382","summary":null,"start":13303539,"end":13308907,"strand":1,"description":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]"}, {"versioned_ensembl_gene_id":"ENSG00000172399.5","gene_symbol":"MYOZ2","gene_name":"myozenin 2 [Source:HGNC Symbol;Acc:HGNC:1330]","synonyms":"C4orf5,CS-1","biotype":"protein_coding","ncbi_id":"51778","summary":"The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder. [provided by RefSeq, Aug 2011]","start":119135784,"end":119187789,"strand":1,"description":"myozenin 2 [Source:HGNC Symbol;Acc:HGNC:1330]"}, {"versioned_ensembl_gene_id":"ENSG00000229971.1","gene_symbol":"AL022313.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36552165,"end":36552700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228723.6","gene_symbol":"SRGAP3-AS2","gene_name":"SRGAP3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40899]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927416","summary":null,"start":9192493,"end":9194453,"strand":1,"description":"SRGAP3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40899]"}, {"versioned_ensembl_gene_id":"ENSG00000260070.1","gene_symbol":"AC006960.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36319775,"end":36320479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237639.2","gene_symbol":"AC064862.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57650521,"end":57650854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000086712.12","gene_symbol":"TXLNG","gene_name":"taxilin gamma [Source:HGNC Symbol;Acc:HGNC:18578]","synonyms":"TXLNGX,MGC126625,MGC126621,LSR5,FLJ11209,FIAT,CXorf15","biotype":"protein_coding","ncbi_id":"55787","summary":"This gene encodes a member of the taxilin family. The encoded protein binds to the C-terminal coiled-coil region of syntaxin family members 1A, 3A and 4A, and may play a role in intracellular vesicle trafficking. This gene is up-regulated by lipopolysaccharide and the gene product may be involved in cell cycle regulation. The related mouse protein was also shown to inhibit activating transcription factor 4-mediated transcription and thus regulate bone mass accrual. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":16786427,"end":16844519,"strand":1,"description":"taxilin gamma [Source:HGNC Symbol;Acc:HGNC:18578]"}, {"versioned_ensembl_gene_id":"ENSG00000253606.2","gene_symbol":"AFG3L2P1","gene_name":"AFG3 like AAA ATPase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24169]","synonyms":"AFG3L2P","biotype":"processed_pseudogene","ncbi_id":"347028","summary":null,"start":43270198,"end":43271960,"strand":-1,"description":"AFG3 like AAA ATPase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24169]"}, {"versioned_ensembl_gene_id":"ENSG00000236982.1","gene_symbol":"BLOC1S2P1","gene_name":"biogenesis of lysosomal organelles complex-1, subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51427]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131924","summary":null,"start":64726748,"end":64727048,"strand":-1,"description":"biogenesis of lysosomal organelles complex-1, subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51427]"}, {"versioned_ensembl_gene_id":"ENSG00000182111.8","gene_symbol":"ZNF716","gene_name":"zinc finger protein 716 [Source:HGNC Symbol;Acc:HGNC:32458]","synonyms":"FLJ46189","biotype":"protein_coding","ncbi_id":"441234","summary":null,"start":57450177,"end":57473546,"strand":1,"description":"zinc finger protein 716 [Source:HGNC Symbol;Acc:HGNC:32458]"}, {"versioned_ensembl_gene_id":"ENSG00000277581.1","gene_symbol":"AL023803.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38962472,"end":38962993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000020633.18","gene_symbol":"RUNX3","gene_name":"runt related transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10473]","synonyms":"PEBP2A3,CBFA3,AML2","biotype":"protein_coding","ncbi_id":"864","summary":"This gene encodes a member of the runt domain-containing family of transcription factors. A heterodimer of this protein and a beta subunit forms a complex that binds to the core DNA sequence 5'-PYGPYGGT-3' found in a number of enhancers and promoters, and can either activate or suppress transcription. It also interacts with other transcription factors. It functions as a tumor suppressor, and the gene is frequently deleted or transcriptionally silenced in cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":24899511,"end":24965121,"strand":-1,"description":"runt related transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:10473]"}, {"versioned_ensembl_gene_id":"ENSG00000215441.3","gene_symbol":"CTAGE12P","gene_name":"CTAGE family member 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:37297]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392298","summary":null,"start":27608382,"end":27610745,"strand":-1,"description":"CTAGE family member 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:37297]"}, {"versioned_ensembl_gene_id":"ENSG00000232688.1","gene_symbol":"LINC01628","gene_name":"long intergenic non-protein coding RNA 1628 [Source:HGNC Symbol;Acc:HGNC:52259]","synonyms":"AC007403.1","biotype":"lincRNA","ncbi_id":"102724321","summary":null,"start":66921510,"end":66922457,"strand":-1,"description":"long intergenic non-protein coding RNA 1628 [Source:HGNC Symbol;Acc:HGNC:52259]"}, {"versioned_ensembl_gene_id":"ENSG00000120563.8","gene_symbol":"LYZL1","gene_name":"lysozyme like 1 [Source:HGNC Symbol;Acc:HGNC:30502]","synonyms":"MGC33408,LYC2","biotype":"protein_coding","ncbi_id":"84569","summary":null,"start":29289061,"end":29318328,"strand":1,"description":"lysozyme like 1 [Source:HGNC Symbol;Acc:HGNC:30502]"}, {"versioned_ensembl_gene_id":"ENSG00000279803.1","gene_symbol":"AC009090.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":57142652,"end":57144936,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225947.1","gene_symbol":"AL596448.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72470374,"end":72471076,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265833.1","gene_symbol":"AC130289.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27707178,"end":27707250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234787.7","gene_symbol":"LINC00458","gene_name":"long intergenic non-protein coding RNA 458 [Source:HGNC Symbol;Acc:HGNC:42807]","synonyms":"LncRNA-ES3","biotype":"lincRNA","ncbi_id":"100507428","summary":null,"start":54115783,"end":54132866,"strand":-1,"description":"long intergenic non-protein coding RNA 458 [Source:HGNC Symbol;Acc:HGNC:42807]"}, {"versioned_ensembl_gene_id":"ENSG00000264689.1","gene_symbol":"AC015688.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27682476,"end":27682737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134193.14","gene_symbol":"REG4","gene_name":"regenerating family member 4 [Source:HGNC Symbol;Acc:HGNC:22977]","synonyms":"RELP,REG-IV,GISP","biotype":"protein_coding","ncbi_id":"83998","summary":null,"start":119794018,"end":119811660,"strand":-1,"description":"regenerating family member 4 [Source:HGNC Symbol;Acc:HGNC:22977]"}, {"versioned_ensembl_gene_id":"ENSG00000257802.1","gene_symbol":"AC089984.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71849228,"end":71850428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204682.5","gene_symbol":"CASC10","gene_name":"cancer susceptibility 10 [Source:HGNC Symbol;Acc:HGNC:31448]","synonyms":"C10orf114,bA418C1.3","biotype":"protein_coding","ncbi_id":"399726","summary":null,"start":21492658,"end":21497262,"strand":-1,"description":"cancer susceptibility 10 [Source:HGNC Symbol;Acc:HGNC:31448]"}, {"versioned_ensembl_gene_id":"ENSG00000246560.2","gene_symbol":"AC018797.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":102828055,"end":102844075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000047648.21","gene_symbol":"ARHGAP6","gene_name":"Rho GTPase activating protein 6 [Source:HGNC Symbol;Acc:HGNC:676]","synonyms":"rhoGAPX-1","biotype":"protein_coding","ncbi_id":"395","summary":"This gene encodes a member of the rhoGAP family of proteins which play a role in the regulation of actin polymerization at the plasma membrane during several cellular processes. This protein is thought to have two independent functions, one as a GTPase-activating protein with specificity for RhoA, and another as a cytoskeletal protein that promotes actin remodeling. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":11137543,"end":11665701,"strand":-1,"description":"Rho GTPase activating protein 6 [Source:HGNC Symbol;Acc:HGNC:676]"}, {"versioned_ensembl_gene_id":"ENSG00000067057.16","gene_symbol":"PFKP","gene_name":"phosphofructokinase, platelet [Source:HGNC Symbol;Acc:HGNC:8878]","synonyms":"PFKF,PFK-C","biotype":"protein_coding","ncbi_id":"5214","summary":"This gene encodes a member of the phosphofructokinase A protein family. The encoded enzyme is the platelet-specific isoform of phosphofructokinase and plays a key role in glycolysis regulation. This gene may play a role in metabolic reprogramming in some cancers, including clear cell renal cell carcinomas, and cancer of the bladder, breast, and lung. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":3066333,"end":3137712,"strand":1,"description":"phosphofructokinase, platelet [Source:HGNC Symbol;Acc:HGNC:8878]"}, {"versioned_ensembl_gene_id":"ENSG00000240024.5","gene_symbol":"LINC00888","gene_name":"long intergenic non-protein coding RNA 888 [Source:HGNC Symbol;Acc:HGNC:48575]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100505687","summary":null,"start":183447608,"end":183456013,"strand":1,"description":"long intergenic non-protein coding RNA 888 [Source:HGNC Symbol;Acc:HGNC:48575]"}, {"versioned_ensembl_gene_id":"ENSG00000205937.11","gene_symbol":"RNPS1","gene_name":"RNA binding protein with serine rich domain 1 [Source:HGNC Symbol;Acc:HGNC:10080]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10921","summary":"This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein binds to the mRNA and remains bound after nuclear export, acting as a nucleocytoplasmic shuttling protein. This protein contains many serine residues. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":2253116,"end":2268412,"strand":-1,"description":"RNA binding protein with serine rich domain 1 [Source:HGNC Symbol;Acc:HGNC:10080]"}, {"versioned_ensembl_gene_id":"ENSG00000206459.2","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31129969,"end":31131783,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000262217.3","gene_symbol":"SLC5A8","gene_name":"solute carrier family 5 member 8 [Source:HGNC Symbol;Acc:HGNC:19119]","synonyms":"AIT","biotype":"protein_coding","ncbi_id":"160728","summary":"SLC5A8 has been shown to transport iodide by a passive mechanism (Rodriguez et al., 2002 [PubMed 12107270]) and monocarboxylates and short-chain fatty acids by a sodium-coupled mechanism (Gopal et al., 2004 [PubMed 15322102]). In kidney, SLC5A8 functions as a high-affinity sodium-coupled lactate transporter involved in reabsorption of lactate and maintenance of blood lactate levels (Thangaraju et al., 2006 [PubMed 16873376]).[supplied by OMIM, Dec 2008]","start":101161669,"end":101216388,"strand":-1,"description":"solute carrier family 5 member 8 [Source:HGNC Symbol;Acc:HGNC:19119]"}, {"versioned_ensembl_gene_id":"ENSG00000136068.14","gene_symbol":"FLNB","gene_name":"filamin B [Source:HGNC Symbol;Acc:HGNC:3755]","synonyms":"TAP,TABP,LRS1,FLN1L,FH1,ABP-278","biotype":"protein_coding","ncbi_id":"2317","summary":"This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3; boomerang dysplasia; autosomal dominant Larsen syndrome; and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Nov 2009]","start":58008400,"end":58172251,"strand":1,"description":"filamin B [Source:HGNC Symbol;Acc:HGNC:3755]"}, {"versioned_ensembl_gene_id":"ENSG00000233167.1","gene_symbol":"EEF1A1P26","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37899]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128637","summary":null,"start":14190795,"end":14192157,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:37899]"}, {"versioned_ensembl_gene_id":"ENSG00000258230.2","gene_symbol":"AC063950.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":101773114,"end":101773755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110514.19","gene_symbol":"MADD","gene_name":"MAP kinase activating death domain [Source:HGNC Symbol;Acc:HGNC:6766]","synonyms":"RAB3GEP,KIAA0358,DENN","biotype":"protein_coding","ncbi_id":"8567","summary":"Tumor necrosis factor alpha (TNF-alpha) is a signaling molecule that interacts with one of two receptors on cells targeted for apoptosis. The apoptotic signal is transduced inside these cells by cytoplasmic adaptor proteins. The protein encoded by this gene is a death domain-containing adaptor protein that interacts with the death domain of TNF-alpha receptor 1 to activate mitogen-activated protein kinase (MAPK) and propagate the apoptotic signal. It is membrane-bound and expressed at a higher level in neoplastic cells than in normal cells. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":47269161,"end":47330031,"strand":1,"description":"MAP kinase activating death domain [Source:HGNC Symbol;Acc:HGNC:6766]"}, {"versioned_ensembl_gene_id":"ENSG00000226685.4","gene_symbol":"CT47A12","gene_name":"cancer/testis antigen family 47, member A12 [Source:HGNC Symbol;Acc:HGNC:33292]","synonyms":"CT47.12","biotype":"protein_coding","ncbi_id":"100507170","summary":null,"start":120930250,"end":120932301,"strand":-1,"description":"cancer/testis antigen family 47, member A12 [Source:HGNC Symbol;Acc:HGNC:33292]"}, {"versioned_ensembl_gene_id":"ENSG00000122547.10","gene_symbol":"EEPD1","gene_name":"endonuclease/exonuclease/phosphatase family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22223]","synonyms":"KIAA1706","biotype":"protein_coding","ncbi_id":"80820","summary":null,"start":36153149,"end":36301543,"strand":1,"description":"endonuclease/exonuclease/phosphatase family domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22223]"}, {"versioned_ensembl_gene_id":"ENSG00000220793.5","gene_symbol":"AC087190.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9156402,"end":9156881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166073.10","gene_symbol":"GPR176","gene_name":"G protein-coupled receptor 176 [Source:HGNC Symbol;Acc:HGNC:32370]","synonyms":"Gm1012","biotype":"protein_coding","ncbi_id":"11245","summary":"Members of the G protein-coupled receptor family, such as GPR176, are cell surface receptors involved in responses to hormones, growth factors, and neurotransmitters (Hata et al., 1995 [PubMed 7893747]).[supplied by OMIM, Jul 2008]","start":39799032,"end":39920892,"strand":-1,"description":"G protein-coupled receptor 176 [Source:HGNC Symbol;Acc:HGNC:32370]"}, {"versioned_ensembl_gene_id":"ENSG00000197251.3","gene_symbol":"LINC00336","gene_name":"long intergenic non-protein coding RNA 336 [Source:HGNC Symbol;Acc:HGNC:33813]","synonyms":"NCRNA00336,FLJ43752,C6orf227","biotype":"lincRNA","ncbi_id":"401253","summary":null,"start":33586106,"end":33593338,"strand":-1,"description":"long intergenic non-protein coding RNA 336 [Source:HGNC Symbol;Acc:HGNC:33813]"}, {"versioned_ensembl_gene_id":"ENSG00000277141.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117243212,"end":117243508,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000143257.11","gene_symbol":"NR1I3","gene_name":"nuclear receptor subfamily 1 group I member 3 [Source:HGNC Symbol;Acc:HGNC:7969]","synonyms":"MB67,CAR1,CAR","biotype":"protein_coding","ncbi_id":"9970","summary":"This gene encodes a member of the nuclear receptor superfamily, and is a key regulator of xenobiotic and endobiotic metabolism. The protein binds to DNA as a monomer or a heterodimer with the retinoid X receptor and regulates the transcription of target genes involved in drug metabolism and bilirubin clearance, such as cytochrome P450 family members. Unlike most nuclear receptors, this transcriptional regulator is constitutively active in the absence of ligand but is regulated by both agonists and inverse agonists. Ligand binding results in translocation of this protein to the nucleus, where it activates or represses target gene transcription. These ligands include bilirubin, a variety of foreign compounds, steroid hormones, and prescription drugs. In addition to drug metabolism, the CAR protein is also reported to regulate genes involved in glucose metabolism, lipid metabolism, cell proliferation, and circadian clock regulation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2020]","start":161229666,"end":161238302,"strand":-1,"description":"nuclear receptor subfamily 1 group I member 3 [Source:HGNC Symbol;Acc:HGNC:7969]"}, {"versioned_ensembl_gene_id":"ENSG00000171611.9","gene_symbol":"PTCRA","gene_name":"pre T-cell antigen receptor alpha [Source:HGNC Symbol;Acc:HGNC:21290]","synonyms":"PTA,PT-ALPHA","biotype":"protein_coding","ncbi_id":"171558","summary":"The protein encoded by this gene is a single-pass type I membrane protein that is found in immmature but not mature T-cells. Along with TCRB and CD3 complex, the encoded protein forms the pre-T-cell receptor complex, which regulates early T-cell development. Four transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2011]","start":42915989,"end":42925835,"strand":1,"description":"pre T-cell antigen receptor alpha [Source:HGNC Symbol;Acc:HGNC:21290]"}, {"versioned_ensembl_gene_id":"ENSG00000282004.1","gene_symbol":"ABCB10P4","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132289","summary":null,"start":28648137,"end":28650318,"strand":-1,"description":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]"}, {"versioned_ensembl_gene_id":"ENSG00000152465.17","gene_symbol":"NMT2","gene_name":"N-myristoyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:7858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9397","summary":"This gene encodes one of two N-myristoyltransferase proteins. N-terminal myristoylation is a lipid modification that is involved in regulating the function and localization of signaling proteins. The encoded protein catalyzes the addition of a myristoyl group to the N-terminal glycine residue of many signaling proteins, including the human immunodeficiency virus type 1 (HIV-1) proteins, Gag and Nef. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":15102584,"end":15168693,"strand":-1,"description":"N-myristoyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:7858]"}, {"versioned_ensembl_gene_id":"ENSG00000226502.2","gene_symbol":"KRT8P27","gene_name":"keratin 8 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33379]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442455","summary":null,"start":64623117,"end":64624573,"strand":1,"description":"keratin 8 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:33379]"}, {"versioned_ensembl_gene_id":"ENSG00000170144.20","gene_symbol":"HNRNPA3","gene_name":"heterogeneous nuclear ribonucleoprotein A3 [Source:HGNC Symbol;Acc:HGNC:24941]","synonyms":"HNRPA3","biotype":"protein_coding","ncbi_id":"220988","summary":null,"start":177212563,"end":177223958,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 [Source:HGNC Symbol;Acc:HGNC:24941]"}, {"versioned_ensembl_gene_id":"ENSG00000197780.9","gene_symbol":"TAF13","gene_name":"TATA-box binding protein associated factor 13 [Source:HGNC Symbol;Acc:HGNC:11546]","synonyms":"TAFII18,TAF2K","biotype":"protein_coding","ncbi_id":"6884","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes a small subunit associated with a subset of TFIID complexes. This subunit interacts with TBP and with two other small subunits of TFIID, TAF10 and TAF11. There is a pseudogene located on chromosome 6. [provided by RefSeq, Jul 2008]","start":109062486,"end":109076002,"strand":-1,"description":"TATA-box binding protein associated factor 13 [Source:HGNC Symbol;Acc:HGNC:11546]"}, {"versioned_ensembl_gene_id":"ENSG00000181744.8","gene_symbol":"C3orf58","gene_name":"chromosome 3 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:28490]","synonyms":"MGC33365,HASF,DIA1","biotype":"protein_coding","ncbi_id":"205428","summary":null,"start":143971798,"end":144048719,"strand":1,"description":"chromosome 3 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:28490]"}, {"versioned_ensembl_gene_id":"ENSG00000278516.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156107,"end":54160227,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000172468.13","gene_symbol":"HSFY1","gene_name":"heat shock transcription factor, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:18568]","synonyms":"HSFY,HSF2L","biotype":"protein_coding","ncbi_id":"86614","summary":"This gene encodes a member of the heat shock factor (HSF) family of transcriptional activators for heat shock proteins. This gene is a candidate gene for azoospermia, since it localizes to a region of chromosome Y that is sometimes deleted in infertile males. The genome has two identical copies of this gene within a palindromic region; this record represents the more centromeric copy. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":18546671,"end":18588963,"strand":1,"description":"heat shock transcription factor, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:18568]"}, {"versioned_ensembl_gene_id":"ENSG00000235131.1","gene_symbol":"AL136528.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3712200,"end":3714298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282660.1","gene_symbol":"AC243913.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28585644,"end":28585769,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146350.13","gene_symbol":"TBC1D32","gene_name":"TBC1 domain family member 32 [Source:HGNC Symbol;Acc:HGNC:21485]","synonyms":"dJ310J6.1,C6orf171,C6orf170,BROMI,bA57L9.1,FLJ34235,FLJ30899","biotype":"protein_coding","ncbi_id":"221322","summary":"This gene encodes a TBC-domain containing protein. Studies of a similar protein in mouse and zebrafish suggest that the encoded protein is involved in sonic hedgehog signaling, and that it interacts with and stabilizes cell cycle-related kinase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":121079494,"end":121334745,"strand":-1,"description":"TBC1 domain family member 32 [Source:HGNC Symbol;Acc:HGNC:21485]"}, {"versioned_ensembl_gene_id":"ENSG00000105131.7","gene_symbol":"EPHX3","gene_name":"epoxide hydrolase 3 [Source:HGNC Symbol;Acc:HGNC:23760]","synonyms":"FLJ22408,ABHD9","biotype":"protein_coding","ncbi_id":"79852","summary":null,"start":15226919,"end":15233435,"strand":-1,"description":"epoxide hydrolase 3 [Source:HGNC Symbol;Acc:HGNC:23760]"}, {"versioned_ensembl_gene_id":"ENSG00000246705.4","gene_symbol":"H2AFJ","gene_name":"H2A histone family member J [Source:HGNC Symbol;Acc:HGNC:14456]","synonyms":"MGC921,FLJ10903","biotype":"protein_coding","ncbi_id":"55766","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is located on chromosome 12 and encodes a replication-independent histone that is a variant H2A histone. The protein is divergent at the C-terminus compared to the consensus H2A histone family member. This gene also encodes an antimicrobial peptide with antibacterial and antifungal activity.[provided by RefSeq, Oct 2015]","start":14774383,"end":14778002,"strand":1,"description":"H2A histone family member J [Source:HGNC Symbol;Acc:HGNC:14456]"}, {"versioned_ensembl_gene_id":"ENSG00000231911.1","gene_symbol":"TPRKBP1","gene_name":"TP53RK binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44943]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060176","summary":null,"start":28658987,"end":28659467,"strand":1,"description":"TP53RK binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44943]"}, {"versioned_ensembl_gene_id":"ENSG00000152804.10","gene_symbol":"HHEX","gene_name":"hematopoietically expressed homeobox [Source:HGNC Symbol;Acc:HGNC:4901]","synonyms":"PRHX,HOX11L-PEN,HEX","biotype":"protein_coding","ncbi_id":"3087","summary":"This gene encodes a member of the homeobox family of transcription factors, many of which are involved in developmental processes. Expression in specific hematopoietic lineages suggests that this protein may play a role in hematopoietic differentiation. [provided by RefSeq, Jul 2008]","start":92689951,"end":92695646,"strand":1,"description":"hematopoietically expressed homeobox [Source:HGNC Symbol;Acc:HGNC:4901]"}, {"versioned_ensembl_gene_id":"ENSG00000158874.11","gene_symbol":"APOA2","gene_name":"apolipoprotein A2 [Source:HGNC Symbol;Acc:HGNC:601]","synonyms":null,"biotype":"protein_coding","ncbi_id":"336","summary":"This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia. [provided by RefSeq, Jul 2008]","start":161222292,"end":161223631,"strand":-1,"description":"apolipoprotein A2 [Source:HGNC Symbol;Acc:HGNC:601]"}, {"versioned_ensembl_gene_id":"ENSG00000111049.3","gene_symbol":"MYF5","gene_name":"myogenic factor 5 [Source:HGNC Symbol;Acc:HGNC:7565]","synonyms":"bHLHc2","biotype":"protein_coding","ncbi_id":"4617","summary":null,"start":80716912,"end":80719673,"strand":1,"description":"myogenic factor 5 [Source:HGNC Symbol;Acc:HGNC:7565]"}, {"versioned_ensembl_gene_id":"ENSG00000282060.1","gene_symbol":"AC243913.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28552131,"end":28552283,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267333.1","gene_symbol":"ASNSP6","gene_name":"asparagine synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49876]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100423060","summary":null,"start":11745626,"end":11747581,"strand":1,"description":"asparagine synthetase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49876]"}, {"versioned_ensembl_gene_id":"ENSG00000132952.11","gene_symbol":"USPL1","gene_name":"ubiquitin specific peptidase like 1 [Source:HGNC Symbol;Acc:HGNC:20294]","synonyms":"D13S106E,C13orf22,bA121O19.1","biotype":"protein_coding","ncbi_id":"10208","summary":null,"start":30617693,"end":30660770,"strand":1,"description":"ubiquitin specific peptidase like 1 [Source:HGNC Symbol;Acc:HGNC:20294]"}, {"versioned_ensembl_gene_id":"ENSG00000197837.3","gene_symbol":"HIST4H4","gene_name":"histone cluster 4 H4 [Source:HGNC Symbol;Acc:HGNC:20510]","synonyms":"MGC24116","biotype":"protein_coding","ncbi_id":"121504","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. [provided by RefSeq, Aug 2015]","start":14767999,"end":14771131,"strand":-1,"description":"histone cluster 4 H4 [Source:HGNC Symbol;Acc:HGNC:20510]"}, {"versioned_ensembl_gene_id":"ENSG00000241258.6","gene_symbol":"CRCP","gene_name":"CGRP receptor component [Source:HGNC Symbol;Acc:HGNC:17888]","synonyms":"RCP9,RCP,CGRP-RCP","biotype":"protein_coding","ncbi_id":"27297","summary":"This gene encodes a membrane protein that functions as part of a receptor complex for a small neuropeptide that increases intracellular cAMP levels. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":66114604,"end":66154568,"strand":1,"description":"CGRP receptor component [Source:HGNC Symbol;Acc:HGNC:17888]"}, {"versioned_ensembl_gene_id":"ENSG00000234500.1","gene_symbol":"AC008267.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":66511556,"end":66545066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232273.1","gene_symbol":"FTH1P1","gene_name":"ferritin heavy chain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3979]","synonyms":"FTHL1","biotype":"processed_pseudogene","ncbi_id":"2496","summary":null,"start":37544763,"end":37545294,"strand":1,"description":"ferritin heavy chain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3979]"}, {"versioned_ensembl_gene_id":"ENSG00000235162.8","gene_symbol":"C12orf75","gene_name":"chromosome 12 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:35164]","synonyms":"OCC1,OCC-1,AGD3","biotype":"protein_coding","ncbi_id":"387882","summary":null,"start":105235290,"end":105396097,"strand":1,"description":"chromosome 12 open reading frame 75 [Source:HGNC Symbol;Acc:HGNC:35164]"}, {"versioned_ensembl_gene_id":"ENSG00000230651.7","gene_symbol":"RGPD4-AS1","gene_name":"RGPD4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49273]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729121","summary":null,"start":107823063,"end":107826891,"strand":-1,"description":"RGPD4 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49273]"}, {"versioned_ensembl_gene_id":"ENSG00000280035.1","gene_symbol":"AC011676.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":141224288,"end":141226947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254019.1","gene_symbol":"AC011676.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141254565,"end":141256817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232228.1","gene_symbol":"AC092431.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69594741,"end":69595058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281612.1","gene_symbol":"AC226496.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68797305,"end":68807118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215179.5","gene_symbol":"AC026241.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46972476,"end":46974617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240477.1","gene_symbol":"AC022494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150050729,"end":150051456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101438.3","gene_symbol":"SLC32A1","gene_name":"solute carrier family 32 member 1 [Source:HGNC Symbol;Acc:HGNC:11018]","synonyms":"VIAAT,VGAT,bA122O1.1","biotype":"protein_coding","ncbi_id":"140679","summary":"The protein encoded by this gene is an integral membrane protein involved in gamma-aminobutyric acid (GABA) and glycine uptake into synaptic vesicles. The encoded protein is a member of amino acid/polyamine transporter family II. [provided by RefSeq, Jul 2008]","start":38724462,"end":38729372,"strand":1,"description":"solute carrier family 32 member 1 [Source:HGNC Symbol;Acc:HGNC:11018]"}, {"versioned_ensembl_gene_id":"ENSG00000155592.15","gene_symbol":"ZKSCAN2","gene_name":"zinc finger with KRAB and SCAN domains 2 [Source:HGNC Symbol;Acc:HGNC:25677]","synonyms":"ZNF694,FLJ23199,ZSCAN34","biotype":"protein_coding","ncbi_id":"342357","summary":null,"start":25236001,"end":25257931,"strand":-1,"description":"zinc finger with KRAB and SCAN domains 2 [Source:HGNC Symbol;Acc:HGNC:25677]"}, {"versioned_ensembl_gene_id":"ENSG00000255108.1","gene_symbol":"AP006621.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":823634,"end":832883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162980.16","gene_symbol":"ARL5A","gene_name":"ADP ribosylation factor like GTPase 5A [Source:HGNC Symbol;Acc:HGNC:696]","synonyms":"ARL5","biotype":"protein_coding","ncbi_id":"26225","summary":"The protein encoded by this gene belongs to the ARF family of GTP-binding proteins. With its distinctive nuclear/nucleolar localization and interaction with HP1alpha, the protein is developmentally regulated and may play a role(s) in nuclear dynamics and/or signaling cascades during embryonic development. Alternative splicing results in multiple transcript variants encoding different isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Jul 2008]","start":151788984,"end":151828492,"strand":-1,"description":"ADP ribosylation factor like GTPase 5A [Source:HGNC Symbol;Acc:HGNC:696]"}, {"versioned_ensembl_gene_id":"ENSG00000177700.5","gene_symbol":"POLR2L","gene_name":"RNA polymerase II subunit L [Source:HGNC Symbol;Acc:HGNC:9199]","synonyms":"RPB7.6,RPB10beta,RPABC5,RBP10,hsRPB10b,hRPB7.6","biotype":"protein_coding","ncbi_id":"5441","summary":"This gene encodes a subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene contains four conserved cysteines characteristic of an atypical zinc-binding domain. Like its counterpart in yeast, this subunit may be shared by the other two DNA-directed RNA polymerases. [provided by RefSeq, Jul 2008]","start":837356,"end":842545,"strand":-1,"description":"RNA polymerase II subunit L [Source:HGNC Symbol;Acc:HGNC:9199]"}, {"versioned_ensembl_gene_id":"ENSG00000213588.5","gene_symbol":"ZBTB9","gene_name":"zinc finger and BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28323]","synonyms":"ZNF919,MGC23166","biotype":"protein_coding","ncbi_id":"221504","summary":null,"start":33453970,"end":33457548,"strand":1,"description":"zinc finger and BTB domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28323]"}, {"versioned_ensembl_gene_id":"ENSG00000274106.1","gene_symbol":"AC008463.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20844829,"end":20853768,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239840.1","gene_symbol":"RPL23AP72","gene_name":"ribosomal protein L23a pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:35736]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271621","summary":null,"start":47150132,"end":47150566,"strand":-1,"description":"ribosomal protein L23a pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:35736]"}, {"versioned_ensembl_gene_id":"ENSG00000236611.1","gene_symbol":"LINC02556","gene_name":"long intergenic non-protein coding RNA 2556 [Source:HGNC Symbol;Acc:HGNC:53595]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724679","summary":null,"start":23326616,"end":23328493,"strand":1,"description":"long intergenic non-protein coding RNA 2556 [Source:HGNC Symbol;Acc:HGNC:53595]"}, {"versioned_ensembl_gene_id":"ENSG00000126010.5","gene_symbol":"GRPR","gene_name":"gastrin releasing peptide receptor [Source:HGNC Symbol;Acc:HGNC:4609]","synonyms":"BB2R,BB2","biotype":"protein_coding","ncbi_id":"2925","summary":"Gastrin-releasing peptide (GRP) regulates numerous functions of the gastrointestinal and central nervous systems, including release of gastrointestinal hormones, smooth muscle cell contraction, and epithelial cell proliferation and is a potent mitogen for neoplastic tissues. The effects of GRP are mediated through the gastrin-releasing peptide receptor. This receptor is a glycosylated, 7-transmembrane G-protein coupled receptor that activates the phospholipase C signaling pathway. The receptor is aberrantly expressed in numerous cancers such as those of the lung, colon, and prostate. An individual with autism and multiple exostoses was found to have a balanced translocation between chromosome 8 and a chromosome X breakpoint located within the gastrin-releasing peptide receptor gene. [provided by RefSeq, Jul 2008]","start":16123556,"end":16153021,"strand":1,"description":"gastrin releasing peptide receptor [Source:HGNC Symbol;Acc:HGNC:4609]"}, {"versioned_ensembl_gene_id":"ENSG00000283839.1","gene_symbol":"AC096667.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":184593577,"end":184599008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213120.3","gene_symbol":"LIN28AP1","gene_name":"LIN28A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38055]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"129402","summary":null,"start":183260642,"end":183261046,"strand":1,"description":"LIN28A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38055]"}, {"versioned_ensembl_gene_id":"ENSG00000170222.11","gene_symbol":"ADPRM","gene_name":"ADP-ribose/CDP-alcohol diphosphatase, manganese dependent [Source:HGNC Symbol;Acc:HGNC:30925]","synonyms":"MDS006,C17orf48","biotype":"protein_coding","ncbi_id":"56985","summary":null,"start":10697594,"end":10711233,"strand":1,"description":"ADP-ribose/CDP-alcohol diphosphatase, manganese dependent [Source:HGNC Symbol;Acc:HGNC:30925]"}, {"versioned_ensembl_gene_id":"ENSG00000280649.2","gene_symbol":"AC245100.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":148458814,"end":148459871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240813.2","gene_symbol":"AC015908.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10745553,"end":10746543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274560.1","gene_symbol":"AC010205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101696002,"end":101696450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234605.2","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31182466,"end":31184282,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000236036.1","gene_symbol":"LINC00445","gene_name":"long intergenic non-protein coding RNA 445 [Source:HGNC Symbol;Acc:HGNC:42782]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507114","summary":null,"start":35697524,"end":35699256,"strand":1,"description":"long intergenic non-protein coding RNA 445 [Source:HGNC Symbol;Acc:HGNC:42782]"}, {"versioned_ensembl_gene_id":"ENSG00000244171.4","gene_symbol":"PBX2P1","gene_name":"PBX homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8635]","synonyms":"PBXP1,PBX2","biotype":"processed_pseudogene","ncbi_id":"5088","summary":null,"start":143176327,"end":143177617,"strand":1,"description":"PBX homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:8635]"}, {"versioned_ensembl_gene_id":"ENSG00000242574.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32934629,"end":32941070,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000229107.2","gene_symbol":"ABHD17AP4","gene_name":"abhydrolase domain containing 17A pseudogene P4 [Source:HGNC Symbol;Acc:HGNC:34042]","synonyms":"FAM108A5P,FAM108A5","biotype":"processed_pseudogene","ncbi_id":"729495","summary":null,"start":20667836,"end":20670984,"strand":-1,"description":"abhydrolase domain containing 17A pseudogene P4 [Source:HGNC Symbol;Acc:HGNC:34042]"}, {"versioned_ensembl_gene_id":"ENSG00000143278.3","gene_symbol":"F13B","gene_name":"coagulation factor XIII B chain [Source:HGNC Symbol;Acc:HGNC:3534]","synonyms":"FXIIIB","biotype":"protein_coding","ncbi_id":"2165","summary":"This gene encodes coagulation factor XIII B subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as a plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon activation by the cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]","start":197039191,"end":197067267,"strand":-1,"description":"coagulation factor XIII B chain [Source:HGNC Symbol;Acc:HGNC:3534]"}, {"versioned_ensembl_gene_id":"ENSG00000282487.1","gene_symbol":"IGHD6-19","gene_name":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]","synonyms":"IGHD619","biotype":"IG_D_gene","ncbi_id":"28486","summary":null,"start":105892470,"end":105892490,"strand":-1,"description":"immunoglobulin heavy diversity 6-19 [Source:HGNC Symbol;Acc:HGNC:5515]"}, {"versioned_ensembl_gene_id":"ENSG00000256162.2","gene_symbol":"SMLR1","gene_name":"small leucine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:44670]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507203","summary":null,"start":130827406,"end":130837135,"strand":1,"description":"small leucine rich protein 1 [Source:HGNC Symbol;Acc:HGNC:44670]"}, {"versioned_ensembl_gene_id":"ENSG00000235642.1","gene_symbol":"PTP4A1P5","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41932]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289380","summary":null,"start":27427777,"end":27428231,"strand":-1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41932]"}, {"versioned_ensembl_gene_id":"ENSG00000260438.1","gene_symbol":"AC018552.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57713782,"end":57714957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226694.2","gene_symbol":"AL441943.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2071845,"end":2081097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091262.15","gene_symbol":"ABCC6","gene_name":"ATP binding cassette subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:57]","synonyms":"PXE,MRP6,MLP1,EST349056,ARA,URG7","biotype":"protein_coding","ncbi_id":"368","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). The encoded protein, a member of the MRP subfamily, is involved in multi-drug resistance. Mutations in this gene cause pseudoxanthoma elasticum. Alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Jul 2008]","start":16148928,"end":16223522,"strand":-1,"description":"ATP binding cassette subfamily C member 6 [Source:HGNC Symbol;Acc:HGNC:57]"}, {"versioned_ensembl_gene_id":"ENSG00000166912.16","gene_symbol":"MTMR10","gene_name":"myotubularin related protein 10 [Source:HGNC Symbol;Acc:HGNC:25999]","synonyms":"FLJ20313,FLJ20313","biotype":"protein_coding","ncbi_id":"54893","summary":null,"start":30938941,"end":30991607,"strand":-1,"description":"myotubularin related protein 10 [Source:HGNC Symbol;Acc:HGNC:25999]"}, {"versioned_ensembl_gene_id":"ENSG00000225336.2","gene_symbol":"HMGB3P1","gene_name":"high mobility group box 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16240]","synonyms":"HMGB3L1,HMG4L,dJ18C9.3","biotype":"processed_pseudogene","ncbi_id":"128872","summary":null,"start":34833575,"end":34834462,"strand":-1,"description":"high mobility group box 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16240]"}, {"versioned_ensembl_gene_id":"ENSG00000279741.1","gene_symbol":"AC007342.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53389886,"end":53390563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280027.1","gene_symbol":"AC007342.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53391089,"end":53392473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223666.2","gene_symbol":"FKBPL","gene_name":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]","synonyms":"DIR1,WISp39,NG7","biotype":"protein_coding","ncbi_id":"63943","summary":"The protein encoded by this gene has similarity to the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The encoded protein is thought to have a potential role in the induced radioresistance. Also it appears to have some involvement in the control of the cell cycle. [provided by RefSeq, Jul 2008]","start":32205134,"end":32206718,"strand":-1,"description":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]"}, {"versioned_ensembl_gene_id":"ENSG00000205758.11","gene_symbol":"CRYZL1","gene_name":"crystallin zeta like 1 [Source:HGNC Symbol;Acc:HGNC:2420]","synonyms":"QOH-1,4P11","biotype":"protein_coding","ncbi_id":"9946","summary":"This gene encodes a protein that has sequence similarity to zeta crystallin, also known as quinone oxidoreductase. This zeta crystallin-like protein also contains an NAD(P)H binding site. Alternatively spliced transcript variants have been observed but their full-length nature has not been completely determined. [provided by RefSeq, Jul 2008]","start":33589341,"end":33643926,"strand":-1,"description":"crystallin zeta like 1 [Source:HGNC Symbol;Acc:HGNC:2420]"}, {"versioned_ensembl_gene_id":"ENSG00000142330.19","gene_symbol":"CAPN10","gene_name":"calpain 10 [Source:HGNC Symbol;Acc:HGNC:1477]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11132","summary":"Calpains represent a ubiquitous, well-conserved family of calcium-dependent cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large catalytic subunit has four domains: domain I, the N-terminal regulatory domain that is processed upon calpain activation; domain II, the protease domain; domain III, a linker domain of unknown function; and domain IV, the calmodulin-like calcium-binding domain. This gene encodes a large subunit. It is an atypical calpain in that it lacks the calmodulin-like calcium-binding domain and instead has a divergent C-terminal domain. It is similar in organization to calpains 5 and 6. This gene is associated with type 2 or non-insulin-dependent diabetes mellitus (NIDDM), and is located within the NIDDM1 region. Multiple alternative transcript variants have been described for this gene. [provided by RefSeq, Sep 2010]","start":240586716,"end":240617705,"strand":1,"description":"calpain 10 [Source:HGNC Symbol;Acc:HGNC:1477]"}, {"versioned_ensembl_gene_id":"ENSG00000278091.4","gene_symbol":"ZNF85","gene_name":"zinc finger protein 85 [Source:HGNC Symbol;Acc:HGNC:13160]","synonyms":"HTF1,HPF4","biotype":"protein_coding","ncbi_id":"7639","summary":null,"start":20929638,"end":20957113,"strand":1,"description":"zinc finger protein 85 [Source:HGNC Symbol;Acc:HGNC:13160]"}, {"versioned_ensembl_gene_id":"ENSG00000224687.1","gene_symbol":"RASAL2-AS1","gene_name":"RASAL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44170]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100302401","summary":null,"start":178091508,"end":178093984,"strand":-1,"description":"RASAL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44170]"}, {"versioned_ensembl_gene_id":"ENSG00000125910.5","gene_symbol":"S1PR4","gene_name":"sphingosine-1-phosphate receptor 4 [Source:HGNC Symbol;Acc:HGNC:3170]","synonyms":"EDG6","biotype":"protein_coding","ncbi_id":"8698","summary":"This gene is a member of the endothelial differentiation, G-protein-coupled (EDG)) receptor gene family. EDG receptors bind lysophospholipids or lysosphingolipids as ligands, and are involved in cell signalling in many different cell types. This EDG receptor gene is intronless and is specifically expressed in the lymphoid tissue. [provided by RefSeq, Jul 2008]","start":3172346,"end":3180332,"strand":1,"description":"sphingosine-1-phosphate receptor 4 [Source:HGNC Symbol;Acc:HGNC:3170]"}, {"versioned_ensembl_gene_id":"ENSG00000226881.5","gene_symbol":"H3F3AP5","gene_name":"H3 histone, family 3A, pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42981]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347376","summary":null,"start":50905438,"end":50905866,"strand":1,"description":"H3 histone, family 3A, pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42981]"}, {"versioned_ensembl_gene_id":"ENSG00000162949.16","gene_symbol":"CAPN13","gene_name":"calpain 13 [Source:HGNC Symbol;Acc:HGNC:16663]","synonyms":"FLJ23523","biotype":"protein_coding","ncbi_id":"92291","summary":"The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes a member of the calpain large subunit family. [provided by RefSeq, Jun 2012]","start":30722771,"end":30820542,"strand":-1,"description":"calpain 13 [Source:HGNC Symbol;Acc:HGNC:16663]"}, {"versioned_ensembl_gene_id":"ENSG00000122707.11","gene_symbol":"RECK","gene_name":"reversion inducing cysteine rich protein with kazal motifs [Source:HGNC Symbol;Acc:HGNC:11345]","synonyms":"ST15,hRECK","biotype":"protein_coding","ncbi_id":"8434","summary":"The protein encoded by this gene is a cysteine-rich, extracellular protein with protease inhibitor-like domains whose expression is suppressed strongly in many tumors and cells transformed by various kinds of oncogenes. In normal cells, this membrane-anchored glycoprotein may serve as a negative regulator for matrix metalloproteinase-9, a key enzyme involved in tumor invasion and metastasis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":36036433,"end":36124451,"strand":1,"description":"reversion inducing cysteine rich protein with kazal motifs [Source:HGNC Symbol;Acc:HGNC:11345]"}, {"versioned_ensembl_gene_id":"ENSG00000227401.1","gene_symbol":"RPL37P1","gene_name":"ribosomal protein L37 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16337]","synonyms":"bA563A22B.2","biotype":"processed_pseudogene","ncbi_id":"140696","summary":null,"start":35588324,"end":35588607,"strand":1,"description":"ribosomal protein L37 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16337]"}, {"versioned_ensembl_gene_id":"ENSG00000261797.1","gene_symbol":"AC073878.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141512698,"end":141513183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244646.4","gene_symbol":"XKRY2","gene_name":"XK related, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23922]","synonyms":"XKRYP7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"353515","summary":"This probable pseudogene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It is similar to the XK (X-linked Kell blood group precursor) gene, which encodes a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more telomeric copy. [provided by RefSeq, Nov 2020]","start":18128610,"end":18137029,"strand":1,"description":"XK related, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:23922]"}, {"versioned_ensembl_gene_id":"ENSG00000263682.1","gene_symbol":"AP005139.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11326270,"end":11328832,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259675.1","gene_symbol":"AC018618.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61639349,"end":61715171,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250604.1","gene_symbol":"AC098679.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":158199105,"end":158200442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255000.1","gene_symbol":"AC139103.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145047860,"end":145048889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259447.1","gene_symbol":"AC013652.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39300418,"end":39310782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225895.1","gene_symbol":"TRAPPC2P8","gene_name":"trafficking protein particle complex 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37731]","synonyms":"TRAPPC2P3B","biotype":"unprocessed_pseudogene","ncbi_id":"414751","summary":null,"start":18105314,"end":18108102,"strand":1,"description":"trafficking protein particle complex 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37731]"}, {"versioned_ensembl_gene_id":"ENSG00000259731.2","gene_symbol":"AC022929.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38756552,"end":38759413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125997.5","gene_symbol":"BPIFB9P","gene_name":"BPI fold containing family B member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:16109]","synonyms":"C20orf115,dJ1187J4.2","biotype":"transcribed_unitary_pseudogene","ncbi_id":"402016","summary":null,"start":33347720,"end":33354444,"strand":1,"description":"BPI fold containing family B member 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:16109]"}, {"versioned_ensembl_gene_id":"ENSG00000224486.1","gene_symbol":"AL662795.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30359278,"end":30359911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233378.1","gene_symbol":"USP9YP34","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:38778]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387361","summary":null,"start":17984349,"end":17993260,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:38778]"}, {"versioned_ensembl_gene_id":"ENSG00000261778.1","gene_symbol":"AC006362.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":141173043,"end":141173216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204990.3","gene_symbol":"AC005692.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":141414383,"end":141416390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261624.1","gene_symbol":"NDUFB10P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52273]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075304","summary":null,"start":141351977,"end":141352768,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52273]"}, {"versioned_ensembl_gene_id":"ENSG00000227993.9","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32388087,"end":32393254,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000105339.10","gene_symbol":"DENND3","gene_name":"DENN domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29134]","synonyms":"KIAA0870","biotype":"protein_coding","ncbi_id":"22898","summary":null,"start":141117278,"end":141195808,"strand":1,"description":"DENN domain containing 3 [Source:HGNC Symbol;Acc:HGNC:29134]"}, {"versioned_ensembl_gene_id":"ENSG00000241293.1","gene_symbol":"PPATP1","gene_name":"phosphoribosyl pyrophosphate amidotransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9239]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289640","summary":null,"start":87051192,"end":87052738,"strand":-1,"description":"phosphoribosyl pyrophosphate amidotransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9239]"}, {"versioned_ensembl_gene_id":"ENSG00000235507.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29704757,"end":29705179,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000254224.1","gene_symbol":"AP003465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":96235427,"end":96238034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156467.9","gene_symbol":"UQCRB","gene_name":"ubiquinol-cytochrome c reductase binding protein [Source:HGNC Symbol;Acc:HGNC:12582]","synonyms":"UQCR6,UQBP,QP-C,QCR7","biotype":"protein_coding","ncbi_id":"7381","summary":"This gene encodes a subunit of the ubiquinol-cytochrome c oxidoreductase complex, which consists of one mitochondrial-encoded and 10 nuclear-encoded subunits. The protein encoded by this gene binds ubiquinone and participates in the transfer of electrons when ubiquinone is bound. This protein plays an important role in hypoxia-induced angiogenesis through mitochondrial reactive oxygen species-mediated signaling. Mutations in this gene are associated with mitochondrial complex III deficiency. Alternatively spliced transcript variants have been found for this gene. Related pseudogenes have been identified on chromosomes 1, 5 and X. [provided by RefSeq, Dec 2011]","start":96225920,"end":96235634,"strand":-1,"description":"ubiquinol-cytochrome c reductase binding protein [Source:HGNC Symbol;Acc:HGNC:12582]"}, {"versioned_ensembl_gene_id":"ENSG00000213999.15","gene_symbol":"MEF2B","gene_name":"myocyte enhancer factor 2B [Source:HGNC Symbol;Acc:HGNC:6995]","synonyms":"RSRFR2","biotype":"protein_coding","ncbi_id":"100271849","summary":"The product of this gene is a member of the MADS/MEF2 family of DNA binding proteins. The protein is thought to regulate gene expression, including expression of the smooth muscle myosin heavy chain gene. This region undergoes considerable alternative splicing, with transcripts supporting two non-overlapping loci (GeneID 729991 and 100271849) as well as numerous read-through transcripts that span both loci (annotated as GeneID 4207). Several isoforms of this protein are expressed from either this locus or from some of the read-through transcripts annotated on GeneID 4207. [provided by RefSeq, Jan 2014]","start":19145568,"end":19170289,"strand":-1,"description":"myocyte enhancer factor 2B [Source:HGNC Symbol;Acc:HGNC:6995]"}, {"versioned_ensembl_gene_id":"ENSG00000231179.9","gene_symbol":"MICB","gene_name":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]","synonyms":"PERB11.2","biotype":"protein_coding","ncbi_id":"4277","summary":"This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor. Binding of the ligand activates the cytolytic response of natural killer (NK) cells, CD8 alphabeta T cells, and gammadelta T cells which express the receptor. This protein is stress-induced and is similar to MHC class I molecules; however, it does not associate with beta-2-microglobulin or bind peptides. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":31561856,"end":31578081,"strand":1,"description":"MHC class I polypeptide-related sequence B [Source:HGNC Symbol;Acc:HGNC:7091]"}, {"versioned_ensembl_gene_id":"ENSG00000234884.1","gene_symbol":"AL022329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25561117,"end":25564462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135631.16","gene_symbol":"RAB11FIP5","gene_name":"RAB11 family interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:24845]","synonyms":"RIP11,pp75,KIAA0857,GAF1","biotype":"protein_coding","ncbi_id":"26056","summary":null,"start":73073382,"end":73156721,"strand":-1,"description":"RAB11 family interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:24845]"}, {"versioned_ensembl_gene_id":"ENSG00000259099.2","gene_symbol":"AC025574.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56380361,"end":56382711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182871.14","gene_symbol":"COL18A1","gene_name":"collagen type XVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2195]","synonyms":"KS,KNO1,KNO","biotype":"protein_coding","ncbi_id":"80781","summary":"This gene encodes the alpha chain of type XVIII collagen. This collagen is one of the multiplexins, extracellular matrix proteins that contain multiple triple-helix domains (collagenous domains) interrupted by non-collagenous domains. A long isoform of the protein has an N-terminal domain that is homologous to the extracellular part of frizzled receptors. Proteolytic processing at several endogenous cleavage sites in the C-terminal domain results in production of endostatin, a potent antiangiogenic protein that is able to inhibit angiogenesis and tumor growth. Mutations in this gene are associated with Knobloch syndrome. The main features of this syndrome involve retinal abnormalities, so type XVIII collagen may play an important role in retinal structure and in neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":45405137,"end":45513720,"strand":1,"description":"collagen type XVIII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2195]"}, {"versioned_ensembl_gene_id":"ENSG00000270665.1","gene_symbol":"HNRNPA1P67","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48797]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728019","summary":null,"start":72807267,"end":72808192,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 67 [Source:HGNC Symbol;Acc:HGNC:48797]"}, {"versioned_ensembl_gene_id":"ENSG00000234418.1","gene_symbol":"AC015983.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122216347,"end":122218437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213302.3","gene_symbol":"AC015983.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122234531,"end":122234903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224405.1","gene_symbol":"LINC00572","gene_name":"long intergenic non-protein coding RNA 572 [Source:HGNC Symbol;Acc:HGNC:43722]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861573","summary":null,"start":29918647,"end":29926651,"strand":-1,"description":"long intergenic non-protein coding RNA 572 [Source:HGNC Symbol;Acc:HGNC:43722]"}, {"versioned_ensembl_gene_id":"ENSG00000198414.5","gene_symbol":"TATDN2P1","gene_name":"TatD DNase domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39254]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131103","summary":null,"start":44283916,"end":44286246,"strand":1,"description":"TatD DNase domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39254]"}, {"versioned_ensembl_gene_id":"ENSG00000235291.7","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"CAT53,p99,FB19,PNUTS","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30678854,"end":30697067,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000236221.9","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"TNXBS,XBS,TNXB1,XB,TNXB2","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32104206,"end":32137613,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000279364.1","gene_symbol":"AC114546.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34978351,"end":34980084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279215.1","gene_symbol":"AC009414.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36360778,"end":36361147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274881.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54705130,"end":54709430,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000168564.5","gene_symbol":"CDKN2AIP","gene_name":"CDKN2A interacting protein [Source:HGNC Symbol;Acc:HGNC:24325]","synonyms":"FLJ20036,CARF","biotype":"protein_coding","ncbi_id":"55602","summary":"The protein encoded by this gene regulates the DNA damage response through several different signaling pathways. One such pathway is the p53-HDM2-p21(WAF1) pathway, which is critical to the DNA damage response. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":183444591,"end":183448198,"strand":1,"description":"CDKN2A interacting protein [Source:HGNC Symbol;Acc:HGNC:24325]"}, {"versioned_ensembl_gene_id":"ENSG00000196652.11","gene_symbol":"ZKSCAN5","gene_name":"zinc finger with KRAB and SCAN domains 5 [Source:HGNC Symbol;Acc:HGNC:12867]","synonyms":"ZSCAN37,ZNF914,ZFP95","biotype":"protein_coding","ncbi_id":"23660","summary":"This gene encodes a zinc finger protein of the Kruppel family. The protein contains a SCAN box and a KRAB A domain and may be involved in transcriptional regulation. A similar protein in mouse is differentially expressed in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":99504651,"end":99534700,"strand":1,"description":"zinc finger with KRAB and SCAN domains 5 [Source:HGNC Symbol;Acc:HGNC:12867]"}, {"versioned_ensembl_gene_id":"ENSG00000107362.13","gene_symbol":"ABHD17B","gene_name":"abhydrolase domain containing 17B [Source:HGNC Symbol;Acc:HGNC:24278]","synonyms":"C9orf77,FAM108B1,CGI-67","biotype":"protein_coding","ncbi_id":"51104","summary":null,"start":71862452,"end":71910931,"strand":-1,"description":"abhydrolase domain containing 17B [Source:HGNC Symbol;Acc:HGNC:24278]"}, {"versioned_ensembl_gene_id":"ENSG00000158019.20","gene_symbol":"BABAM2","gene_name":"BRISC and BRCA1 A complex member 2 [Source:HGNC Symbol;Acc:HGNC:1106]","synonyms":"BRE,BRCC45,BRCC4","biotype":"protein_coding","ncbi_id":"9577","summary":"This gene encodes an anti-apoptotic, death receptor-associated protein that interacts with tumor necrosis factor-receptor-1. The encoded protein acts as an adapter in several protein complexes, including the BRCA1-A complex and the BRISC complex. The BRCA1-A complex possesses ubiquitinase activity and targets sites of double strand DNA breaks, while the BRISC complex exhibits deubiquitinase activity and is involved in mitotic spindle assembly. This gene is upregulated in several types of cancer. [provided by RefSeq, Jun 2016]","start":27889941,"end":28338901,"strand":1,"description":"BRISC and BRCA1 A complex member 2 [Source:HGNC Symbol;Acc:HGNC:1106]"}, {"versioned_ensembl_gene_id":"ENSG00000276194.4","gene_symbol":"HNF1B","gene_name":"HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]","synonyms":"VHNF1,TCF2,MODY5,LFB3,HNF1beta","biotype":"protein_coding","ncbi_id":"6928","summary":"This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":37690967,"end":37749771,"strand":-1,"description":"HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]"}, {"versioned_ensembl_gene_id":"ENSG00000231519.1","gene_symbol":"AC007285.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30069658,"end":30075115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137834.14","gene_symbol":"SMAD6","gene_name":"SMAD family member 6 [Source:HGNC Symbol;Acc:HGNC:6772]","synonyms":"MADH6,HsT17432,MADH7","biotype":"protein_coding","ncbi_id":"4091","summary":"The protein encoded by this gene belongs to the SMAD family of proteins, which are related to Drosophila 'mothers against decapentaplegic' (Mad) and C. elegans Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein functions in the negative regulation of BMP and TGF-beta/activin-signalling. Multiple transcript variants have been found for this gene.[provided by RefSeq, Sep 2014]","start":66702228,"end":66782848,"strand":1,"description":"SMAD family member 6 [Source:HGNC Symbol;Acc:HGNC:6772]"}, {"versioned_ensembl_gene_id":"ENSG00000214867.3","gene_symbol":"SRSF9P1","gene_name":"serine and arginine rich splicing factor 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10792]","synonyms":"SFRS9P1","biotype":"processed_pseudogene","ncbi_id":"54021","summary":null,"start":36295173,"end":36295702,"strand":-1,"description":"serine and arginine rich splicing factor 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10792]"}, {"versioned_ensembl_gene_id":"ENSG00000267627.5","gene_symbol":"AC118757.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35951803,"end":35966118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065057.7","gene_symbol":"NTHL1","gene_name":"nth like DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:8028]","synonyms":"OCTS3,NTH1","biotype":"protein_coding","ncbi_id":"4913","summary":"The protein encoded by this gene is a DNA N-glycosylase of the endonuclease III family. Like a similar protein in E. coli, the encoded protein has DNA glycosylase activity on DNA substrates containing oxidized pyrimidine residues and has apurinic/apyrimidinic lyase activity. [provided by RefSeq, Oct 2008]","start":2039815,"end":2047866,"strand":-1,"description":"nth like DNA glycosylase 1 [Source:HGNC Symbol;Acc:HGNC:8028]"}, {"versioned_ensembl_gene_id":"ENSG00000235154.1","gene_symbol":"FP325330.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48044710,"end":48048549,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271271.5","gene_symbol":"UGT2A2","gene_name":"UDP glucuronosyltransferase family 2 member A2 [Source:HGNC Symbol;Acc:HGNC:28183]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574537","summary":null,"start":69589309,"end":69639642,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member A2 [Source:HGNC Symbol;Acc:HGNC:28183]"}, {"versioned_ensembl_gene_id":"ENSG00000130164.13","gene_symbol":"LDLR","gene_name":"low density lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:6547]","synonyms":"LDLCQ2","biotype":"protein_coding","ncbi_id":"3949","summary":"The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. Low density lipoprotein (LDL) is normally bound at the cell membrane and taken into the cell ending up in lysosomes where the protein is degraded and the cholesterol is made available for repression of microsomal enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the rate-limiting step in cholesterol synthesis. At the same time, a reciprocal stimulation of cholesterol ester synthesis takes place. Mutations in this gene cause the autosomal dominant disorder, familial hypercholesterolemia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]","start":11089362,"end":11133816,"strand":1,"description":"low density lipoprotein receptor [Source:HGNC Symbol;Acc:HGNC:6547]"}, {"versioned_ensembl_gene_id":"ENSG00000215478.8","gene_symbol":"CES5AP1","gene_name":"carboxylesterase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38516]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"649264","summary":null,"start":23359603,"end":23387731,"strand":-1,"description":"carboxylesterase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38516]"}, {"versioned_ensembl_gene_id":"ENSG00000253681.1","gene_symbol":"AC013509.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":76576551,"end":76579345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255686.1","gene_symbol":"AC073864.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":117453012,"end":117456986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223654.3","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30791619,"end":30794413,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000141101.12","gene_symbol":"NOB1","gene_name":"NIN1/PSMD8 binding protein 1 homolog [Source:HGNC Symbol;Acc:HGNC:29540]","synonyms":"PSMD8BP1,NOB1P,MST158,ART-4","biotype":"protein_coding","ncbi_id":"28987","summary":"In yeast, over 200 protein and RNA cofactors are required for ribosome assembly, and these are generally conserved in eukaryotes. These factors orchestrate modification and cleavage of the initial 35S precursor rRNA transcript into the mature 18S, 5.8S, and 25S rRNAs, folding of the rRNA, and binding of ribosomal proteins and 5S RNA. Nob1 is involved in pre-rRNA processing. In a late cytoplasmic processing step, Nob1 cleaves a 20S rRNA intermediate at cleavage site D to produce the mature 18S rRNA (Lamanna and Karbstein, 2009 [PubMed 19706509]).[supplied by OMIM, Nov 2010]","start":69741867,"end":69754940,"strand":-1,"description":"NIN1/PSMD8 binding protein 1 homolog [Source:HGNC Symbol;Acc:HGNC:29540]"}, {"versioned_ensembl_gene_id":"ENSG00000278205.1","gene_symbol":"AC092447.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56462536,"end":56467771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250582.1","gene_symbol":"SMAD1-AS2","gene_name":"SMAD1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:49381]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927659","summary":null,"start":145497073,"end":145502971,"strand":-1,"description":"SMAD1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:49381]"}, {"versioned_ensembl_gene_id":"ENSG00000237268.2","gene_symbol":"AC092447.7","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56421857,"end":56448375,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259471.1","gene_symbol":"LINC01169","gene_name":"long intergenic non-protein coding RNA 1169 [Source:HGNC Symbol;Acc:HGNC:49541]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723165","summary":null,"start":66582190,"end":66685794,"strand":1,"description":"long intergenic non-protein coding RNA 1169 [Source:HGNC Symbol;Acc:HGNC:49541]"}, {"versioned_ensembl_gene_id":"ENSG00000188693.7","gene_symbol":"CYP51A1-AS1","gene_name":"CYP51A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50694]","synonyms":"LRRD1-AS1,ENST00000453068","biotype":"antisense_RNA","ncbi_id":"613126","summary":null,"start":92134604,"end":92180725,"strand":1,"description":"CYP51A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50694]"}, {"versioned_ensembl_gene_id":"ENSG00000234264.1","gene_symbol":"DEPDC1-AS1","gene_name":"DEPDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50592]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927220","summary":null,"start":68496676,"end":68538627,"strand":1,"description":"DEPDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50592]"}, {"versioned_ensembl_gene_id":"ENSG00000270866.1","gene_symbol":"AC067773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76403998,"end":76405091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231157.3","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"Em:AB014080.4,SUCLA2P","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30459163,"end":30460532,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000261804.1","gene_symbol":"AC007342.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53373493,"end":53384745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278500.1","gene_symbol":"AC009336.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":176151085,"end":176173097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177452.7","gene_symbol":"AL161742.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63788721,"end":63789304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180448.10","gene_symbol":"ARHGAP45","gene_name":"Rho GTPase activating protein 45 [Source:HGNC Symbol;Acc:HGNC:17102]","synonyms":"KIAA0223,HMHA1,HA-1","biotype":"protein_coding","ncbi_id":"23526","summary":null,"start":1065923,"end":1086628,"strand":1,"description":"Rho GTPase activating protein 45 [Source:HGNC Symbol;Acc:HGNC:17102]"}, {"versioned_ensembl_gene_id":"ENSG00000229276.1","gene_symbol":"REV3L-IT1","gene_name":"REV3L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41377]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106478974","summary":null,"start":111360641,"end":111361607,"strand":-1,"description":"REV3L intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41377]"}, {"versioned_ensembl_gene_id":"ENSG00000105141.5","gene_symbol":"CASP14","gene_name":"caspase 14 [Source:HGNC Symbol;Acc:HGNC:1502]","synonyms":"MICE,MGC119079,MGC119078","biotype":"protein_coding","ncbi_id":"23581","summary":"This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This caspase has been shown to be processed and activated by caspase 8 and caspase 10 in vitro, and by anti-Fas agonist antibody or TNF-related apoptosis inducing ligand in vivo. The expression and processing of this caspase may be involved in keratinocyte terminal differentiation, which is important for the formation of the skin barrier. [provided by RefSeq, Jul 2008]","start":15049384,"end":15058293,"strand":1,"description":"caspase 14 [Source:HGNC Symbol;Acc:HGNC:1502]"}, {"versioned_ensembl_gene_id":"ENSG00000235396.5","gene_symbol":"NOTCH4","gene_name":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]","synonyms":"INT3","biotype":"protein_coding","ncbi_id":"4855","summary":"This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor may play a role in vascular, renal and hepatic development. Mutations in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":32143311,"end":32172533,"strand":-1,"description":"notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]"}, {"versioned_ensembl_gene_id":"ENSG00000115310.17","gene_symbol":"RTN4","gene_name":"reticulon 4 [Source:HGNC Symbol;Acc:HGNC:14085]","synonyms":"NSP-CL,NOGO,KIAA0886,ASY","biotype":"protein_coding","ncbi_id":"57142","summary":"This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. The product of this gene is a potent neurite outgrowth inhibitor which may also help block the regeneration of the central nervous system in higher vertebrates. Alternatively spliced transcript variants derived both from differential splicing and differential promoter usage and encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":54972187,"end":55112621,"strand":-1,"description":"reticulon 4 [Source:HGNC Symbol;Acc:HGNC:14085]"}, {"versioned_ensembl_gene_id":"ENSG00000138078.15","gene_symbol":"PREPL","gene_name":"prolyl endopeptidase-like [Source:HGNC Symbol;Acc:HGNC:30228]","synonyms":"KIAA0436","biotype":"protein_coding","ncbi_id":"9581","summary":"The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene.[provided by RefSeq, Jan 2010]","start":44316281,"end":44361862,"strand":-1,"description":"prolyl endopeptidase-like [Source:HGNC Symbol;Acc:HGNC:30228]"}, {"versioned_ensembl_gene_id":"ENSG00000226468.2","gene_symbol":"AC018641.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32456963,"end":32457758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267303.1","gene_symbol":"AC011511.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10315471,"end":10320678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234056.1","gene_symbol":"LINC00463","gene_name":"long intergenic non-protein coding RNA 463 [Source:HGNC Symbol;Acc:HGNC:42813]","synonyms":"TCONS_l2_00007499,AMER2-AS1","biotype":"lincRNA","ncbi_id":"101928922","summary":null,"start":25172828,"end":25180079,"strand":-1,"description":"long intergenic non-protein coding RNA 463 [Source:HGNC Symbol;Acc:HGNC:42813]"}, {"versioned_ensembl_gene_id":"ENSG00000241929.1","gene_symbol":"AC108751.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149462182,"end":149464830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156096.13","gene_symbol":"UGT2B4","gene_name":"UDP glucuronosyltransferase family 2 member B4 [Source:HGNC Symbol;Acc:HGNC:12553]","synonyms":"UGT2B11","biotype":"protein_coding","ncbi_id":"7363","summary":null,"start":69480165,"end":69526014,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B4 [Source:HGNC Symbol;Acc:HGNC:12553]"}, {"versioned_ensembl_gene_id":"ENSG00000151208.16","gene_symbol":"DLG5","gene_name":"discs large MAGUK scaffold protein 5 [Source:HGNC Symbol;Acc:HGNC:2904]","synonyms":"P-dlg,KIAA0583","biotype":"protein_coding","ncbi_id":"9231","summary":"This gene encodes a member of the family of discs large (DLG) homologs, a subset of the membrane-associated guanylate kinase (MAGUK) superfamily. The MAGUK proteins are composed of a catalytically inactive guanylate kinase domain, in addition to PDZ and SH3 domains, and are thought to function as scaffolding molecules at sites of cell-cell contact. The protein encoded by this gene localizes to the plasma membrane and cytoplasm, and interacts with components of adherens junctions and the cytoskeleton. It is proposed to function in the transmission of extracellular signals to the cytoskeleton and in the maintenance of epithelial cell structure. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":77790791,"end":77926526,"strand":-1,"description":"discs large MAGUK scaffold protein 5 [Source:HGNC Symbol;Acc:HGNC:2904]"}, {"versioned_ensembl_gene_id":"ENSG00000115896.15","gene_symbol":"PLCL1","gene_name":"phospholipase C like 1 (inactive) [Source:HGNC Symbol;Acc:HGNC:9063]","synonyms":"PRIP,PPP1R127,PLCL,PLCE,PLC-L","biotype":"protein_coding","ncbi_id":"5334","summary":null,"start":197804702,"end":198572581,"strand":1,"description":"phospholipase C like 1 (inactive) [Source:HGNC Symbol;Acc:HGNC:9063]"}, {"versioned_ensembl_gene_id":"ENSG00000170293.8","gene_symbol":"CMTM8","gene_name":"CKLF like MARVEL transmembrane domain containing 8 [Source:HGNC Symbol;Acc:HGNC:19179]","synonyms":"CKLFSF8","biotype":"protein_coding","ncbi_id":"152189","summary":"This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 3. This gene acts as a tumor suppressor, and plays a role in regulating the migration of tumor cells. The encoded protein is thought to function as a a negative regulator of epidermal growth factor-induced signaling. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]","start":32238679,"end":32370325,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 8 [Source:HGNC Symbol;Acc:HGNC:19179]"}, {"versioned_ensembl_gene_id":"ENSG00000234737.1","gene_symbol":"KRT18P15","gene_name":"keratin 18 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:32449]","synonyms":"KRT18L5","biotype":"processed_pseudogene","ncbi_id":"729211","summary":null,"start":32258940,"end":32260230,"strand":1,"description":"keratin 18 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:32449]"}, {"versioned_ensembl_gene_id":"ENSG00000231020.1","gene_symbol":"AL591043.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176305672,"end":176306095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115155.16","gene_symbol":"OTOF","gene_name":"otoferlin [Source:HGNC Symbol;Acc:HGNC:8515]","synonyms":"FER1L2,DFNB9,DFNB6","biotype":"protein_coding","ncbi_id":"9381","summary":"Mutations in this gene are a cause of neurosensory nonsyndromic recessive deafness, DFNB9. The short form of the encoded protein has 3 C2 domains, a single carboxy-terminal transmembrane domain found also in the C. elegans spermatogenesis factor FER-1 and human dysferlin, while the long form has 6 C2 domains. The homology suggests that this protein may be involved in vesicle membrane fusion. Several transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":26457203,"end":26558698,"strand":-1,"description":"otoferlin [Source:HGNC Symbol;Acc:HGNC:8515]"}, {"versioned_ensembl_gene_id":"ENSG00000180581.7","gene_symbol":"SRP9P1","gene_name":"signal recognition particle 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23402]","synonyms":"SRP9L1","biotype":"processed_pseudogene","ncbi_id":"653226","summary":null,"start":91807179,"end":91807439,"strand":-1,"description":"signal recognition particle 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23402]"}, {"versioned_ensembl_gene_id":"ENSG00000213205.3","gene_symbol":"STRADBP1","gene_name":"STE20-related kinase adaptor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22478]","synonyms":"STLK6ps1,ALS2CR2P1","biotype":"processed_pseudogene","ncbi_id":"389599","summary":null,"start":150512559,"end":150513839,"strand":-1,"description":"STE20-related kinase adaptor beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22478]"}, {"versioned_ensembl_gene_id":"ENSG00000231712.1","gene_symbol":"AC104698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30209995,"end":30210307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229692.3","gene_symbol":"SOS1-IT1","gene_name":"SOS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41385]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100505911","summary":null,"start":38992279,"end":38993857,"strand":-1,"description":"SOS1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41385]"}, {"versioned_ensembl_gene_id":"ENSG00000251333.3","gene_symbol":"RTN3P1","gene_name":"reticulon 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19212]","synonyms":"RTN3PS","biotype":"processed_pseudogene","ncbi_id":"152905","summary":null,"start":145375543,"end":145376253,"strand":1,"description":"reticulon 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19212]"}, {"versioned_ensembl_gene_id":"ENSG00000232056.1","gene_symbol":"AC092687.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10847577,"end":10854955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183935.5","gene_symbol":"HTR7P1","gene_name":"5-hydroxytryptamine receptor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30411]","synonyms":"HTR7P","biotype":"transcribed_processed_pseudogene","ncbi_id":"93164","summary":null,"start":13000420,"end":13004830,"strand":1,"description":"5-hydroxytryptamine receptor 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30411]"}, {"versioned_ensembl_gene_id":"ENSG00000274618.1","gene_symbol":"HIST1H4F","gene_name":"histone cluster 1 H4 family member f [Source:HGNC Symbol;Acc:HGNC:4783]","synonyms":"H4FC,H4/c,H4","biotype":"protein_coding","ncbi_id":"8361","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26240426,"end":26240737,"strand":1,"description":"histone cluster 1 H4 family member f [Source:HGNC Symbol;Acc:HGNC:4783]"}, {"versioned_ensembl_gene_id":"ENSG00000242258.1","gene_symbol":"LINC00996","gene_name":"long intergenic non-protein coding RNA 996 [Source:HGNC Symbol;Acc:HGNC:27800]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285972","summary":null,"start":150433654,"end":150448140,"strand":1,"description":"long intergenic non-protein coding RNA 996 [Source:HGNC Symbol;Acc:HGNC:27800]"}, {"versioned_ensembl_gene_id":"ENSG00000234289.5","gene_symbol":"H2BFS","gene_name":"H2B histone family member S [Source:HGNC Symbol;Acc:HGNC:4762]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54145","summary":null,"start":43565189,"end":43565648,"strand":1,"description":"H2B histone family member S [Source:HGNC Symbol;Acc:HGNC:4762]"}, {"versioned_ensembl_gene_id":"ENSG00000139508.14","gene_symbol":"SLC46A3","gene_name":"solute carrier family 46 member 3 [Source:HGNC Symbol;Acc:HGNC:27501]","synonyms":"FLJ42613,DKFZp686A1775","biotype":"protein_coding","ncbi_id":"283537","summary":"The protein encoded by this gene is a member of a transmembrane protein family that transports small molecules across membranes. The encoded protein has been found in lysosomal membranes, where it can transport catabolites from the lysosomes to the cytoplasm. This protein has been shown to be an effective transporter of the cytotoxic drug maytansine, which is used in antibody-based targeting of cancer cells. [provided by RefSeq, Dec 2016]","start":28700064,"end":28718970,"strand":-1,"description":"solute carrier family 46 member 3 [Source:HGNC Symbol;Acc:HGNC:27501]"}, {"versioned_ensembl_gene_id":"ENSG00000274508.1","gene_symbol":"AC007336.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55425574,"end":55426130,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205560.12","gene_symbol":"CPT1B","gene_name":"carnitine palmitoyltransferase 1B [Source:HGNC Symbol;Acc:HGNC:2329]","synonyms":"M-CPT1,CPT1-M","biotype":"protein_coding","ncbi_id":"1375","summary":"The protein encoded by this gene, a member of the carnitine/choline acetyltransferase family, is the rate-controlling enzyme of the long-chain fatty acid beta-oxidation pathway in muscle mitochondria. This enzyme is required for the net transport of long-chain fatty acyl-CoAs from the cytoplasm into the mitochondria. Multiple transcript variants encoding different isoforms have been found for this gene, and read-through transcripts are expressed from the upstream locus that include exons from this gene. [provided by RefSeq, Jun 2009]","start":50568861,"end":50578465,"strand":-1,"description":"carnitine palmitoyltransferase 1B [Source:HGNC Symbol;Acc:HGNC:2329]"}, {"versioned_ensembl_gene_id":"ENSG00000237264.4","gene_symbol":"FTH1P11","gene_name":"ferritin heavy chain 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:3981]","synonyms":"FTHL11","biotype":"processed_pseudogene","ncbi_id":"2503","summary":null,"start":81521682,"end":81522232,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:3981]"}, {"versioned_ensembl_gene_id":"ENSG00000281711.1","gene_symbol":"CR854858.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13149474,"end":13152272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166897.14","gene_symbol":"ELFN2","gene_name":"extracellular leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29396]","synonyms":"PPP1R29,PPP1R29,LRRC62,LRRC62,KIAA1904,dJ63G5.3","biotype":"protein_coding","ncbi_id":"114794","summary":null,"start":37367960,"end":37427470,"strand":-1,"description":"extracellular leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29396]"}, {"versioned_ensembl_gene_id":"ENSG00000198768.10","gene_symbol":"APCDD1L","gene_name":"APC down-regulated 1 like [Source:HGNC Symbol;Acc:HGNC:26892]","synonyms":"FLJ90166","biotype":"protein_coding","ncbi_id":"164284","summary":null,"start":58459101,"end":58515131,"strand":-1,"description":"APC down-regulated 1 like [Source:HGNC Symbol;Acc:HGNC:26892]"}, {"versioned_ensembl_gene_id":"ENSG00000251288.2","gene_symbol":"AC018797.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102751401,"end":102752641,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248971.2","gene_symbol":"KRT8P46","gene_name":"keratin 8 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39880]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418744","summary":null,"start":102728746,"end":102730171,"strand":-1,"description":"keratin 8 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:39880]"}, {"versioned_ensembl_gene_id":"ENSG00000254673.1","gene_symbol":"AC110275.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43018424,"end":43077334,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281992.1","gene_symbol":"AC233699.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36242073,"end":36242178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275920.1","gene_symbol":"KRTAP5-3","gene_name":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]","synonyms":"KRTAP5.3,KRTAP5-9","biotype":"protein_coding","ncbi_id":"387266","summary":null,"start":1613275,"end":1614173,"strand":-1,"description":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]"}, {"versioned_ensembl_gene_id":"ENSG00000236892.1","gene_symbol":"AL357833.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3532094,"end":3537031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203739.3","gene_symbol":"AL645568.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173417793,"end":173461362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125827.8","gene_symbol":"TMX4","gene_name":"thioredoxin related transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:25237]","synonyms":"DJ971N18.2,TXNDC13,PDIA14,KIAA1162","biotype":"protein_coding","ncbi_id":"56255","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, a catalytically active thioredoxin domain, one transmembrane domain and C-terminal ASP/GLU-rich calcium binding domain. Unlike most members of this gene family, it lacks a C-terminal ER-retention sequence. The encoded protein has been shown to have reductase activity in vitro. [provided by RefSeq, Jan 2017]","start":7977348,"end":8019829,"strand":-1,"description":"thioredoxin related transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:25237]"}, {"versioned_ensembl_gene_id":"ENSG00000236739.3","gene_symbol":"CLIC4P1","gene_name":"chloride intracellular channel 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49797]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646609","summary":null,"start":22747700,"end":22748234,"strand":1,"description":"chloride intracellular channel 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49797]"}, {"versioned_ensembl_gene_id":"ENSG00000254027.1","gene_symbol":"AC009902.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81279871,"end":81281446,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280787.2","gene_symbol":"HERC2P2","gene_name":"hect domain and RLD 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4870]","synonyms":"D15F37S3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400322","summary":null,"start":22497423,"end":22593430,"strand":1,"description":"hect domain and RLD 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4870]"}, {"versioned_ensembl_gene_id":"ENSG00000227099.1","gene_symbol":"HLA-DRB7","gene_name":"major histocompatibility complex, class II, DR beta 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4955]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3129","summary":null,"start":32627102,"end":32646281,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4955]"}, {"versioned_ensembl_gene_id":"ENSG00000271496.1","gene_symbol":"SNRPGP20","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49376]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480271","summary":null,"start":79989014,"end":79989218,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:49376]"}, {"versioned_ensembl_gene_id":"ENSG00000231119.2","gene_symbol":"AL031666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47352561,"end":47354633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262327.7","gene_symbol":"AGK","gene_name":"acylglycerol kinase [Source:HGNC Symbol;Acc:HGNC:21869]","synonyms":"MULK,FLJ10842","biotype":"protein_coding","ncbi_id":"55750","summary":"The protein encoded by this gene is a mitochondrial membrane protein involved in lipid and glycerolipid metabolism. The encoded protein is a lipid kinase that catalyzes the formation of phosphatidic and lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10. [provided by RefSeq, Feb 2012]","start":141633901,"end":141655244,"strand":1,"description":"acylglycerol kinase [Source:HGNC Symbol;Acc:HGNC:21869]"}, {"versioned_ensembl_gene_id":"ENSG00000256379.2","gene_symbol":"TRAV8-5","gene_name":"T-cell receptor alpha variable 8-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12150]","synonyms":"TRAV85,TCRAV8S5","biotype":"TR_V_pseudogene","ncbi_id":"28681","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21903077,"end":21904598,"strand":1,"description":"T-cell receptor alpha variable 8-5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12150]"}, {"versioned_ensembl_gene_id":"ENSG00000079335.18","gene_symbol":"CDC14A","gene_name":"cell division cycle 14A [Source:HGNC Symbol;Acc:HGNC:1718]","synonyms":"DFNB105,Cdc14A2,Cdc14A1,cdc14","biotype":"protein_coding","ncbi_id":"8556","summary":"The protein encoded by this gene is a member of the dual specificity protein tyrosine phosphatase family. It is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit of cell mitosis and initiation of DNA replication, suggesting a role in cell cycle control. This protein has been shown to interact with, and dephosphorylate tumor suppressor protein p53, and is thought to regulate the function of p53. Alternative splicing of this gene results in several transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":100345025,"end":100520277,"strand":1,"description":"cell division cycle 14A [Source:HGNC Symbol;Acc:HGNC:1718]"}, {"versioned_ensembl_gene_id":"ENSG00000266696.1","gene_symbol":"AC044840.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49205912,"end":49208781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263895.1","gene_symbol":"AC100778.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":49431744,"end":49447420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225590.9","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"SACM2L,ARE1","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33171888,"end":33193647,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000237668.1","gene_symbol":"RPS15AP38","gene_name":"ribosomal protein S15a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36523]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271655","summary":null,"start":36421273,"end":36421644,"strand":-1,"description":"ribosomal protein S15a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36523]"}, {"versioned_ensembl_gene_id":"ENSG00000257465.2","gene_symbol":"ELOCP32","gene_name":"elongin C pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49173]","synonyms":"TCEB1P32","biotype":"processed_pseudogene","ncbi_id":"106481964","summary":null,"start":117245551,"end":117246164,"strand":-1,"description":"elongin C pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49173]"}, {"versioned_ensembl_gene_id":"ENSG00000270736.1","gene_symbol":"AL670379.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120966948,"end":120967199,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271211.1","gene_symbol":"AL670379.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120962087,"end":120962339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278032.2","gene_symbol":"LY6E","gene_name":"lymphocyte antigen 6 family member E [Source:HGNC Symbol;Acc:HGNC:6727]","synonyms":"TSA-1,SCA-2,RIG-E","biotype":"protein_coding","ncbi_id":"4061","summary":null,"start":143017982,"end":143023832,"strand":1,"description":"lymphocyte antigen 6 family member E [Source:HGNC Symbol;Acc:HGNC:6727]"}, {"versioned_ensembl_gene_id":"ENSG00000256917.1","gene_symbol":"AC008033.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68487687,"end":68487863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254623.1","gene_symbol":"DEFB108E","gene_name":"defensin beta 108E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30174]","synonyms":"DEFB108P4","biotype":"unprocessed_pseudogene","ncbi_id":"503840","summary":null,"start":12341426,"end":12345776,"strand":-1,"description":"defensin beta 108E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30174]"}, {"versioned_ensembl_gene_id":"ENSG00000153560.11","gene_symbol":"UBP1","gene_name":"upstream binding protein 1 (LBP-1a) [Source:HGNC Symbol;Acc:HGNC:12507]","synonyms":"LBP-1a","biotype":"protein_coding","ncbi_id":"7342","summary":null,"start":33388336,"end":33441371,"strand":-1,"description":"upstream binding protein 1 (LBP-1a) [Source:HGNC Symbol;Acc:HGNC:12507]"}, {"versioned_ensembl_gene_id":"ENSG00000233751.1","gene_symbol":"AC104772.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":222677677,"end":222678289,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227733.9","gene_symbol":"AC239809.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148159213,"end":148255012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279839.1","gene_symbol":"AL512383.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":3205988,"end":3208664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223605.1","gene_symbol":"AC107399.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":117249924,"end":117250188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203531.3","gene_symbol":"AC104772.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":222698623,"end":222699484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232656.7","gene_symbol":"IDI2-AS1","gene_name":"IDI2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30885]","synonyms":"IDI2-AS,HT009,Em:AC022536.4,C10orf110","biotype":"antisense_RNA","ncbi_id":"55853","summary":null,"start":1022666,"end":1044201,"strand":1,"description":"IDI2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30885]"}, {"versioned_ensembl_gene_id":"ENSG00000213875.3","gene_symbol":"AC005019.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13871856,"end":13872513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256615.1","gene_symbol":"AC010197.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21662313,"end":21760032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185055.10","gene_symbol":"EFCAB10","gene_name":"EF-hand calcium binding domain 10 [Source:HGNC Symbol;Acc:HGNC:34531]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130771","summary":null,"start":105565120,"end":105600875,"strand":-1,"description":"EF-hand calcium binding domain 10 [Source:HGNC Symbol;Acc:HGNC:34531]"}, {"versioned_ensembl_gene_id":"ENSG00000181035.13","gene_symbol":"SLC25A42","gene_name":"solute carrier family 25 member 42 [Source:HGNC Symbol;Acc:HGNC:28380]","synonyms":"MGC26694","biotype":"protein_coding","ncbi_id":"284439","summary":"This gene encodes a solute carrier family 25 protein. Solute carrier family 25 proteins are localized to mitochondria and play critical roles in the transport of molecules across the inner mitochondrial membrane. The encoded protein is a mitochondrial transporter for coenzyme A (CoA) and adenosine 3',5'-diphosphate. [provided by RefSeq, Feb 2012]","start":19063999,"end":19112888,"strand":1,"description":"solute carrier family 25 member 42 [Source:HGNC Symbol;Acc:HGNC:28380]"}, {"versioned_ensembl_gene_id":"ENSG00000136003.15","gene_symbol":"ISCU","gene_name":"iron-sulfur cluster assembly enzyme [Source:HGNC Symbol;Acc:HGNC:29882]","synonyms":"NIFUN,ISU2,IscU,hnifU","biotype":"protein_coding","ncbi_id":"23479","summary":"This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Feb 2016]","start":108562582,"end":108569384,"strand":1,"description":"iron-sulfur cluster assembly enzyme [Source:HGNC Symbol;Acc:HGNC:29882]"}, {"versioned_ensembl_gene_id":"ENSG00000231881.1","gene_symbol":"AL109615.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44073913,"end":44077952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213197.3","gene_symbol":"AC012066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152389937,"end":152390630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223469.1","gene_symbol":"AL157371.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43851757,"end":43852333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279085.1","gene_symbol":"AL022323.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25009685,"end":25015072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283215.1","gene_symbol":"LINC02537","gene_name":"long intergenic non-protein coding RNA 2537 [Source:HGNC Symbol;Acc:HGNC:27784]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285857","summary":null,"start":43844878,"end":43852317,"strand":-1,"description":"long intergenic non-protein coding RNA 2537 [Source:HGNC Symbol;Acc:HGNC:27784]"}, {"versioned_ensembl_gene_id":"ENSG00000271181.1","gene_symbol":"Z99916.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25179309,"end":25179554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226375.1","gene_symbol":"AL022310.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":173174300,"end":173175503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279110.1","gene_symbol":"AL022323.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25052122,"end":25065241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279006.1","gene_symbol":"AL022323.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25048967,"end":25051966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250622.1","gene_symbol":"AC093325.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156972631,"end":156972956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203280.4","gene_symbol":"AL022323.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25102433,"end":25112692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197077.13","gene_symbol":"KIAA1671","gene_name":"KIAA1671 [Source:HGNC Symbol;Acc:HGNC:29345]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85379","summary":null,"start":24952730,"end":25197448,"strand":1,"description":"KIAA1671 [Source:HGNC Symbol;Acc:HGNC:29345]"}, {"versioned_ensembl_gene_id":"ENSG00000181577.15","gene_symbol":"C6orf223","gene_name":"chromosome 6 open reading frame 223 [Source:HGNC Symbol;Acc:HGNC:28692]","synonyms":"MGC45491","biotype":"protein_coding","ncbi_id":"221416","summary":null,"start":44000580,"end":44005958,"strand":1,"description":"chromosome 6 open reading frame 223 [Source:HGNC Symbol;Acc:HGNC:28692]"}, {"versioned_ensembl_gene_id":"ENSG00000271389.1","gene_symbol":"OSBPL9P1","gene_name":"oxysterol binding protein like 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48731]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130821","summary":null,"start":80163327,"end":80164795,"strand":1,"description":"oxysterol binding protein like 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48731]"}, {"versioned_ensembl_gene_id":"ENSG00000237667.5","gene_symbol":"LINC01115","gene_name":"long intergenic non-protein coding RNA 1115 [Source:HGNC Symbol;Acc:HGNC:49258]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339822","summary":null,"start":779840,"end":868426,"strand":-1,"description":"long intergenic non-protein coding RNA 1115 [Source:HGNC Symbol;Acc:HGNC:49258]"}, {"versioned_ensembl_gene_id":"ENSG00000111716.12","gene_symbol":"LDHB","gene_name":"lactate dehydrogenase B [Source:HGNC Symbol;Acc:HGNC:6541]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3945","summary":"This gene encodes the B subunit of lactate dehydrogenase enzyme, which catalyzes the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+ in a post-glycolysis process. Alternatively spliced transcript variants have been found for this gene. Recent studies have shown that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Mutations in this gene are associated with lactate dehydrogenase B deficiency. Pseudogenes have been identified on chromosomes X, 5 and 13. [provided by RefSeq, Feb 2016]","start":21635342,"end":21757857,"strand":-1,"description":"lactate dehydrogenase B [Source:HGNC Symbol;Acc:HGNC:6541]"}, {"versioned_ensembl_gene_id":"ENSG00000270409.1","gene_symbol":"AC090950.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15732252,"end":15733470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239699.1","gene_symbol":"HNRNPA3P8","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48497]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129557","summary":null,"start":80216261,"end":80217234,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48497]"}, {"versioned_ensembl_gene_id":"ENSG00000279465.1","gene_symbol":"AC090950.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15731877,"end":15732536,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242586.1","gene_symbol":"AC108740.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80442081,"end":80442305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231359.3","gene_symbol":"AC072052.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6490793,"end":6491098,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282964.1","gene_symbol":"AC026108.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":102953289,"end":102953835,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271627.1","gene_symbol":"AC027612.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91723023,"end":91723605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280883.1","gene_symbol":"AL078605.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170275331,"end":170276762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250219.2","gene_symbol":"LTV1P1","gene_name":"LTV1 ribosome biogenesis factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44049]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289220","summary":null,"start":120091046,"end":120092282,"strand":-1,"description":"LTV1 ribosome biogenesis factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44049]"}, {"versioned_ensembl_gene_id":"ENSG00000234858.1","gene_symbol":"LINC01149","gene_name":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]","synonyms":"XXbac-BPG181B23.4","biotype":"processed_transcript","ncbi_id":"101929111","summary":null,"start":31432091,"end":31437391,"strand":1,"description":"long intergenic non-protein coding RNA 1149 [Source:HGNC Symbol;Acc:HGNC:39757]"}, {"versioned_ensembl_gene_id":"ENSG00000262488.1","gene_symbol":"AC133065.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10840384,"end":10841544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273539.3","gene_symbol":"IGHV3-73","gene_name":"immunoglobulin heavy variable 3-73 [Source:HGNC Symbol;Acc:HGNC:5623]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28409","summary":null,"start":106826868,"end":106827409,"strand":-1,"description":"immunoglobulin heavy variable 3-73 [Source:HGNC Symbol;Acc:HGNC:5623]"}, {"versioned_ensembl_gene_id":"ENSG00000272468.1","gene_symbol":"AL021807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27122657,"end":27123221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000000005.5","gene_symbol":"TNMD","gene_name":"tenomodulin [Source:HGNC Symbol;Acc:HGNC:17757]","synonyms":"myodulin,ChM1L,BRICD4,tendin,TEM","biotype":"protein_coding","ncbi_id":"64102","summary":"This gene encodes a protein that is related to chondromodulin-I, which is a cartilage-specific glycoprotein that functions to stimulate chondrocyte growth and to inhibit tube formation of endothelial cells. This protein is also an angiogenesis inhibitor. Genetic variation in this gene is associated with a risk for type 2 diabetes, central obesity and serum levels of systemic immune mediators in a body size-dependent manner. This gene is also a candidate gene for age-related macular degeneration, though a direct link has yet to be demonstrated. [provided by RefSeq, Sep 2009]","start":100584802,"end":100599885,"strand":1,"description":"tenomodulin [Source:HGNC Symbol;Acc:HGNC:17757]"}, {"versioned_ensembl_gene_id":"ENSG00000234369.1","gene_symbol":"TATDN1P1","gene_name":"TatD DNase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45058]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728737","summary":null,"start":63222155,"end":63223045,"strand":1,"description":"TatD DNase domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45058]"}, {"versioned_ensembl_gene_id":"ENSG00000272767.1","gene_symbol":"JMJD1C-AS1","gene_name":"JMJD1C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28222]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"84989","summary":null,"start":63465229,"end":63466563,"strand":1,"description":"JMJD1C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:28222]"}, {"versioned_ensembl_gene_id":"ENSG00000257254.1","gene_symbol":"AC010202.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102513251,"end":102513655,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257704.3","gene_symbol":"INAFM1","gene_name":"InaF motif containing 1 [Source:HGNC Symbol;Acc:HGNC:27406]","synonyms":"PRR24","biotype":"protein_coding","ncbi_id":"255783","summary":null,"start":47274453,"end":47275707,"strand":1,"description":"InaF motif containing 1 [Source:HGNC Symbol;Acc:HGNC:27406]"}, {"versioned_ensembl_gene_id":"ENSG00000224368.1","gene_symbol":"ARAFP2","gene_name":"ARAF pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:647]","synonyms":"PKS1,ARAFPS,ARAF2P,ARAF2","biotype":"processed_pseudogene","ncbi_id":"644000","summary":null,"start":63404842,"end":63405400,"strand":-1,"description":"ARAF pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:647]"}, {"versioned_ensembl_gene_id":"ENSG00000177324.13","gene_symbol":"BEND2","gene_name":"BEN domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28509]","synonyms":"MGC33653,CXorf20","biotype":"protein_coding","ncbi_id":"139105","summary":"This gene encodes a protein which has two BEN domains in the C-terminus. These domains are found in proteins which participate in protein and DNA interactions which occur during chromatin restructuring or transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":18162931,"end":18220883,"strand":-1,"description":"BEN domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28509]"}, {"versioned_ensembl_gene_id":"ENSG00000232583.1","gene_symbol":"GPR143P","gene_name":"G protein-coupled receptor 143 pseudogene [Source:HGNC Symbol;Acc:HGNC:18499]","synonyms":"OA1P","biotype":"unprocessed_pseudogene","ncbi_id":"352896","summary":null,"start":7100733,"end":7106502,"strand":-1,"description":"G protein-coupled receptor 143 pseudogene [Source:HGNC Symbol;Acc:HGNC:18499]"}, {"versioned_ensembl_gene_id":"ENSG00000264635.1","gene_symbol":"AP001020.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":738058,"end":739662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204434.5","gene_symbol":"POTEKP","gene_name":"POTE ankyrin domain family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:30182]","synonyms":"POTEK,POTE2delta,FKSG30,ACTBL3","biotype":"unprocessed_pseudogene","ncbi_id":"440915","summary":null,"start":131591752,"end":131627266,"strand":1,"description":"POTE ankyrin domain family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:30182]"}, {"versioned_ensembl_gene_id":"ENSG00000213750.4","gene_symbol":"AP002982.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97624203,"end":97625079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273588.1","gene_symbol":"AC093838.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":131625957,"end":131628147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248027.1","gene_symbol":"AP001351.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100684162,"end":100687955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165895.17","gene_symbol":"ARHGAP42","gene_name":"Rho GTPase activating protein 42 [Source:HGNC Symbol;Acc:HGNC:26545]","synonyms":"GRAF3,FLJ32810","biotype":"protein_coding","ncbi_id":"143872","summary":"This gene encodes a Rho GTPase-activating protein (RhoGAP), and member of the GRAF or BAR-PH family of proteins. Expression of this gene is enriched in vascular smooth muscle cells and the encoded protein inhibits RhoA activity to regulate vascular tone and control blood pressure. A mutation in the first intron of this gene modulates its expression and is associated with reduced blood pressure in human patients with borderline hypertension. [provided by RefSeq, Jul 2017]","start":100687653,"end":100991937,"strand":1,"description":"Rho GTPase activating protein 42 [Source:HGNC Symbol;Acc:HGNC:26545]"}, {"versioned_ensembl_gene_id":"ENSG00000273369.1","gene_symbol":"AC096586.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44693946,"end":44694386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234311.1","gene_symbol":"AL451069.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":132433733,"end":132441484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257259.1","gene_symbol":"LINC02388","gene_name":"long intergenic non-protein coding RNA 2388 [Source:HGNC Symbol;Acc:HGNC:53315]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927653","summary":null,"start":58565960,"end":58781747,"strand":-1,"description":"long intergenic non-protein coding RNA 2388 [Source:HGNC Symbol;Acc:HGNC:53315]"}, {"versioned_ensembl_gene_id":"ENSG00000243813.1","gene_symbol":"AC078857.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121099108,"end":121099774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267716.1","gene_symbol":"AC083760.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44039471,"end":44040140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273210.1","gene_symbol":"AP001437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37365477,"end":37365932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278933.1","gene_symbol":"AC022743.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":43499173,"end":43499836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012817.15","gene_symbol":"KDM5D","gene_name":"lysine demethylase 5D [Source:HGNC Symbol;Acc:HGNC:11115]","synonyms":"KIAA0234,JARID1D,HYA,HY,SMCY","biotype":"protein_coding","ncbi_id":"8284","summary":"This gene encodes a protein containing zinc finger domains. A short peptide derived from this protein is a minor histocompatibility antigen which can lead to graft rejection of male donor cells in a female recipient. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":19703865,"end":19744939,"strand":-1,"description":"lysine demethylase 5D [Source:HGNC Symbol;Acc:HGNC:11115]"}, {"versioned_ensembl_gene_id":"ENSG00000229703.6","gene_symbol":"CR589904.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":248691760,"end":248716755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198491.3","gene_symbol":"AC007920.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":187197090,"end":187207629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073905.8","gene_symbol":"VDAC1P1","gene_name":"voltage dependent anion channel 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12671]","synonyms":"VDAC1P","biotype":"processed_pseudogene","ncbi_id":"642585","summary":null,"start":80929500,"end":80930347,"strand":1,"description":"voltage dependent anion channel 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12671]"}, {"versioned_ensembl_gene_id":"ENSG00000247746.4","gene_symbol":"USP51","gene_name":"ubiquitin specific peptidase 51 [Source:HGNC Symbol;Acc:HGNC:23086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158880","summary":null,"start":55484616,"end":55489202,"strand":-1,"description":"ubiquitin specific peptidase 51 [Source:HGNC Symbol;Acc:HGNC:23086]"}, {"versioned_ensembl_gene_id":"ENSG00000188305.5","gene_symbol":"C19orf35","gene_name":"chromosome 19 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:24793]","synonyms":"FLJ45778","biotype":"protein_coding","ncbi_id":"374872","summary":null,"start":2274622,"end":2282176,"strand":-1,"description":"chromosome 19 open reading frame 35 [Source:HGNC Symbol;Acc:HGNC:24793]"}, {"versioned_ensembl_gene_id":"ENSG00000067369.13","gene_symbol":"TP53BP1","gene_name":"tumor protein p53 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11999]","synonyms":"TDRD30,p202,53BP1","biotype":"protein_coding","ncbi_id":"7158","summary":"This gene encodes a protein that functions in the DNA double-strand break repair pathway choice, promoting non-homologous end joining (NHEJ) pathways, and limiting homologous recombination. This protein plays multiple roles in the DNA damage response, including promoting checkpoint signaling following DNA damage, acting as a scaffold for recruitment of DNA damage response proteins to damaged chromatin, and promoting NHEJ pathways by limiting end resection following a double-strand break. These roles are also important during V(D)J recombination, class switch recombination and at unprotected telomeres. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]","start":43403061,"end":43510728,"strand":-1,"description":"tumor protein p53 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11999]"}, {"versioned_ensembl_gene_id":"ENSG00000275199.4","gene_symbol":"AKT3","gene_name":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]","synonyms":"RAC-gamma,PRKBG,PKBG","biotype":"protein_coding","ncbi_id":"10000","summary":"The protein encoded by this gene is a member of the AKT, also called PKB, serine/threonine protein kinase family. AKT kinases are known to be regulators of cell signaling in response to insulin and growth factors. They are involved in a wide variety of biological processes including cell proliferation, differentiation, apoptosis, tumorigenesis, as well as glycogen synthesis and glucose uptake. This kinase has been shown to be stimulated by platelet-derived growth factor (PDGF), insulin, and insulin-like growth factor 1 (IGF1). Alternatively splice transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":243488233,"end":243855434,"strand":-1,"description":"AKT serine/threonine kinase 3 [Source:HGNC Symbol;Acc:HGNC:393]"}, {"versioned_ensembl_gene_id":"ENSG00000164306.10","gene_symbol":"PRIMPOL","gene_name":"primase and DNA directed polymerase [Source:HGNC Symbol;Acc:HGNC:26575]","synonyms":"FLJ33167,CCDC111","biotype":"protein_coding","ncbi_id":"201973","summary":"This gene encodes a DNA primase-polymerase that belongs to a superfamily of archaeao-eukaryotic primases. Members of this family have primase activity, catalyzing the synthesis of short RNA primers that serve as starting points for DNA synthesis, as well as DNA polymerase activity. The encoded protein facilitates DNA damage tolerance by mediating uninterrupted fork progression after UV irradiation and reinitiating DNA synthesis. An allelic variant in this gene is associated with myopia 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]","start":184649613,"end":184694963,"strand":1,"description":"primase and DNA directed polymerase [Source:HGNC Symbol;Acc:HGNC:26575]"}, {"versioned_ensembl_gene_id":"ENSG00000129493.14","gene_symbol":"HEATR5A","gene_name":"HEAT repeat containing 5A [Source:HGNC Symbol;Acc:HGNC:20276]","synonyms":"DKFZP434I1735,C14orf125","biotype":"protein_coding","ncbi_id":"25938","summary":null,"start":31291791,"end":31420582,"strand":-1,"description":"HEAT repeat containing 5A [Source:HGNC Symbol;Acc:HGNC:20276]"}, {"versioned_ensembl_gene_id":"ENSG00000146556.14","gene_symbol":"WASH2P","gene_name":"WAS protein family homolog 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:33145]","synonyms":"FAM39B,MGC52000","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375260","summary":null,"start":113588550,"end":113599043,"strand":1,"description":"WAS protein family homolog 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:33145]"}, {"versioned_ensembl_gene_id":"ENSG00000203661.4","gene_symbol":"OR2T5","gene_name":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401993","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248488589,"end":248491113,"strand":1,"description":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]"}, {"versioned_ensembl_gene_id":"ENSG00000129480.12","gene_symbol":"DTD2","gene_name":"D-tyrosyl-tRNA deacylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:20277]","synonyms":"MGC9912,C14orf126","biotype":"protein_coding","ncbi_id":"112487","summary":null,"start":31446036,"end":31457510,"strand":-1,"description":"D-tyrosyl-tRNA deacylase 2 (putative) [Source:HGNC Symbol;Acc:HGNC:20277]"}, {"versioned_ensembl_gene_id":"ENSG00000155093.17","gene_symbol":"PTPRN2","gene_name":"protein tyrosine phosphatase, receptor type N2 [Source:HGNC Symbol;Acc:HGNC:9677]","synonyms":"phogrin,KIAA0387,ICAAR,IA-2beta","biotype":"protein_coding","ncbi_id":"5799","summary":"This gene encodes a protein with sequence similarity to receptor-like protein tyrosine phosphatases. However, tyrosine phosphatase activity has not been experimentally validated for this protein. Studies of the rat ortholog suggest that the encoded protein may instead function as a phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4,5-diphosphate, and this function may be involved in the regulation of insulin secretion. This protein has been identified as an autoantigen in insulin-dependent diabetes mellitus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":157539056,"end":158587788,"strand":-1,"description":"protein tyrosine phosphatase, receptor type N2 [Source:HGNC Symbol;Acc:HGNC:9677]"}, {"versioned_ensembl_gene_id":"ENSG00000260466.1","gene_symbol":"AC126696.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":87836532,"end":87837663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005486.16","gene_symbol":"RHBDD2","gene_name":"rhomboid domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23082]","synonyms":"NPD007,RHBDL7","biotype":"protein_coding","ncbi_id":"57414","summary":"The protein encoded by this gene is a member of the rhomboid family of membrane-bound proteases and is overexpressed in some breast cancers. Members of this family are involved in intramembrane proteolysis. In mouse, the orthologous protein associates with the Golgi body. [provided by RefSeq, Sep 2016]","start":75842602,"end":75888926,"strand":1,"description":"rhomboid domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23082]"}, {"versioned_ensembl_gene_id":"ENSG00000071575.11","gene_symbol":"TRIB2","gene_name":"tribbles pseudokinase 2 [Source:HGNC Symbol;Acc:HGNC:30809]","synonyms":"TRB2,GS3955","biotype":"protein_coding","ncbi_id":"28951","summary":"This gene encodes one of three members of the Tribbles family. The Tribbles members share a Trb domain, which is homologous to protein serine-threonine kinases, but lacks the active site lysine and probably lacks a catalytic function. The Tribbles proteins interact and modulate the activity of signal transduction pathways in a number of physiological and pathological processes. This Tribbles member induces apoptosis of cells mainly of the hematopoietic origin. It has been identified as a protein up-regulated by inflammatory stimuli in myeloid (THP-1) cells, and also as an oncogene that inactivates the transcription factor C/EBPalpha (CCAAT/enhancer-binding protein alpha) and causes acute myelogenous leukemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]","start":12716889,"end":12742734,"strand":1,"description":"tribbles pseudokinase 2 [Source:HGNC Symbol;Acc:HGNC:30809]"}, {"versioned_ensembl_gene_id":"ENSG00000266441.1","gene_symbol":"AP005205.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6728821,"end":6729862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166896.7","gene_symbol":"ATP23","gene_name":"ATP23 metallopeptidase and ATP synthase assembly factor homolog [Source:HGNC Symbol;Acc:HGNC:29452]","synonyms":"XRCC6BP1,KUB3","biotype":"protein_coding","ncbi_id":"91419","summary":"The protein encoded by this gene is amplified in glioblastomas and interacts with the DNA binding subunit of DNA-dependent protein kinase. This kinase is involved in double-strand break repair (DSB), and higher expression of the encoded protein increases the efficiency of DSB. In addition, comparison to orthologous proteins strongly suggests that this protein is a metalloprotease important in the biosynthesis of mitochondrial ATPase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":57941541,"end":57957269,"strand":1,"description":"ATP23 metallopeptidase and ATP synthase assembly factor homolog [Source:HGNC Symbol;Acc:HGNC:29452]"}, {"versioned_ensembl_gene_id":"ENSG00000111371.15","gene_symbol":"SLC38A1","gene_name":"solute carrier family 38 member 1 [Source:HGNC Symbol;Acc:HGNC:13447]","synonyms":"NAT2,ATA1,SAT1","biotype":"protein_coding","ncbi_id":"81539","summary":"Amino acid transporters play essential roles in the uptake of nutrients, production of energy, chemical metabolism, detoxification, and neurotransmitter cycling. SLC38A1 is an important transporter of glutamine, an intermediate in the detoxification of ammonia and the production of urea. Glutamine serves as a precursor for the synaptic transmitter, glutamate (Gu et al., 2001 [PubMed 11325958]).[supplied by OMIM, Mar 2008]","start":46183063,"end":46270017,"strand":-1,"description":"solute carrier family 38 member 1 [Source:HGNC Symbol;Acc:HGNC:13447]"}, {"versioned_ensembl_gene_id":"ENSG00000263369.6","gene_symbol":"AC090616.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32106330,"end":32114125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215057.4","gene_symbol":"PKMP5","gene_name":"pyruvate kinase, muscle pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44247]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442156","summary":null,"start":5972412,"end":5974012,"strand":1,"description":"pyruvate kinase, muscle pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44247]"}, {"versioned_ensembl_gene_id":"ENSG00000146839.18","gene_symbol":"ZAN","gene_name":"zonadhesin (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12857]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7455","summary":"This gene encodes a protein that functions in the species specificity of sperm adhesion to the egg zona pellucida. The encoded protein is located in the acrosome and may be involved in signaling or gamete recognition. An allelic polymorphism in this gene results in both functional and frameshifted alleles; the reference genome represents the functional allele. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":100733626,"end":100797797,"strand":1,"description":"zonadhesin (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12857]"}, {"versioned_ensembl_gene_id":"ENSG00000239946.1","gene_symbol":"ZBTB20-AS3","gene_name":"ZBTB20 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:42422]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104413890","summary":null,"start":114873114,"end":114876514,"strand":1,"description":"ZBTB20 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:42422]"}, {"versioned_ensembl_gene_id":"ENSG00000283743.1","gene_symbol":"AL009172.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":47605233,"end":47623509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164675.10","gene_symbol":"IQUB","gene_name":"IQ motif and ubiquitin domain containing [Source:HGNC Symbol;Acc:HGNC:21995]","synonyms":"FLJ35834","biotype":"protein_coding","ncbi_id":"154865","summary":null,"start":123452400,"end":123535077,"strand":-1,"description":"IQ motif and ubiquitin domain containing [Source:HGNC Symbol;Acc:HGNC:21995]"}, {"versioned_ensembl_gene_id":"ENSG00000139197.10","gene_symbol":"PEX5","gene_name":"peroxisomal biogenesis factor 5 [Source:HGNC Symbol;Acc:HGNC:9719]","synonyms":"PXR1,PTS1R","biotype":"protein_coding","ncbi_id":"5830","summary":"The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]","start":7188685,"end":7218574,"strand":1,"description":"peroxisomal biogenesis factor 5 [Source:HGNC Symbol;Acc:HGNC:9719]"}, {"versioned_ensembl_gene_id":"ENSG00000126759.13","gene_symbol":"CFP","gene_name":"complement factor properdin [Source:HGNC Symbol;Acc:HGNC:8864]","synonyms":"PFC","biotype":"protein_coding","ncbi_id":"5199","summary":"This gene encodes a plasma glycoprotein that positively regulates the alternative complement pathway of the innate immune system. This protein binds to many microbial surfaces and apoptotic cells and stabilizes the C3- and C5-convertase enzyme complexes in a feedback loop that ultimately leads to formation of the membrane attack complex and lysis of the target cell. Mutations in this gene result in two forms of properdin deficiency, which results in high susceptibility to meningococcal infections. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Feb 2009]","start":47623172,"end":47630305,"strand":-1,"description":"complement factor properdin [Source:HGNC Symbol;Acc:HGNC:8864]"}, {"versioned_ensembl_gene_id":"ENSG00000185480.11","gene_symbol":"PARPBP","gene_name":"PARP1 binding protein [Source:HGNC Symbol;Acc:HGNC:26074]","synonyms":"PARI,FLJ20641,C12orf48","biotype":"protein_coding","ncbi_id":"55010","summary":null,"start":102120185,"end":102197520,"strand":1,"description":"PARP1 binding protein [Source:HGNC Symbol;Acc:HGNC:26074]"}, {"versioned_ensembl_gene_id":"ENSG00000224786.2","gene_symbol":"CETN4P","gene_name":"centrin 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:35450]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"729338","summary":"Centrins are members of the calcium-binding EF-hand protein superfamily and accumulate in centrosomes. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008]","start":122728532,"end":122732482,"strand":-1,"description":"centrin 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:35450]"}, {"versioned_ensembl_gene_id":"ENSG00000118946.11","gene_symbol":"PCDH17","gene_name":"protocadherin 17 [Source:HGNC Symbol;Acc:HGNC:14267]","synonyms":"PCH68,PCDH68","biotype":"protein_coding","ncbi_id":"27253","summary":"This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein contains six extracellular cadherin domains, a transmembrane domain, and a cytoplasmic tail differing from those of the classical cadherins. The encoded protein may play a role in the establishment and function of specific cell-cell connections in the brain. [provided by RefSeq, Jul 2008]","start":57631810,"end":57729311,"strand":1,"description":"protocadherin 17 [Source:HGNC Symbol;Acc:HGNC:14267]"}, {"versioned_ensembl_gene_id":"ENSG00000254653.1","gene_symbol":"AC024475.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46116578,"end":46117318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227145.1","gene_symbol":"IL21-AS1","gene_name":"IL21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40299]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996941","summary":null,"start":122618983,"end":122689156,"strand":1,"description":"IL21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40299]"}, {"versioned_ensembl_gene_id":"ENSG00000278722.1","gene_symbol":"AL445288.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57632759,"end":57633575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183783.6","gene_symbol":"KCTD8","gene_name":"potassium channel tetramerization domain containing 8 [Source:HGNC Symbol;Acc:HGNC:22394]","synonyms":null,"biotype":"protein_coding","ncbi_id":"386617","summary":null,"start":44173909,"end":44448807,"strand":-1,"description":"potassium channel tetramerization domain containing 8 [Source:HGNC Symbol;Acc:HGNC:22394]"}, {"versioned_ensembl_gene_id":"ENSG00000240925.1","gene_symbol":"AC004263.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120247460,"end":120247791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259055.1","gene_symbol":"AL591770.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51088957,"end":51091288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274768.2","gene_symbol":"CISD3","gene_name":"CDGSH iron sulfur domain 3 [Source:HGNC Symbol;Acc:HGNC:27578]","synonyms":"Miner2","biotype":"protein_coding","ncbi_id":"284106","summary":"CISD3 is a member of the CDGSH domain-containing family, which may play a role in regulating electron transport and oxidative phosphorylation (Wiley et al., 2007 [PubMed 17376863]).[supplied by OMIM, Apr 2008]","start":38531022,"end":38535831,"strand":1,"description":"CDGSH iron sulfur domain 3 [Source:HGNC Symbol;Acc:HGNC:27578]"}, {"versioned_ensembl_gene_id":"ENSG00000280423.1","gene_symbol":"AL359852.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2561947,"end":2564143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279114.1","gene_symbol":"Z99129.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":122471923,"end":122484161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248939.1","gene_symbol":"AC111198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43133867,"end":43234956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170315.13","gene_symbol":"UBB","gene_name":"ubiquitin B [Source:HGNC Symbol;Acc:HGNC:12463]","synonyms":"MGC8385,FLJ25987","biotype":"protein_coding","ncbi_id":"7314","summary":"This gene encodes ubiquitin, one of the most conserved proteins known. Ubiquitin has a major role in targeting cellular proteins for degradation by the 26S proteosome. It is also involved in the maintenance of chromatin structure, the regulation of gene expression, and the stress response. Ubiquitin is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin moiety fused to an unrelated protein. This gene consists of three direct repeats of the ubiquitin coding sequence with no spacer sequence. Consequently, the protein is expressed as a polyubiquitin precursor with a final amino acid after the last repeat. An aberrant form of this protein has been detected in patients with Alzheimer's disease and Down syndrome. Pseudogenes of this gene are located on chromosomes 1, 2, 13, and 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":16380798,"end":16382745,"strand":1,"description":"ubiquitin B [Source:HGNC Symbol;Acc:HGNC:12463]"}, {"versioned_ensembl_gene_id":"ENSG00000254790.1","gene_symbol":"AP000842.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":125940496,"end":125941193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272407.1","gene_symbol":"AL022394.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":41196647,"end":41196938,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233887.1","gene_symbol":"AL354685.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":97847263,"end":97849017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130294.15","gene_symbol":"KIF1A","gene_name":"kinesin family member 1A [Source:HGNC Symbol;Acc:HGNC:888]","synonyms":"C2orf20,ATSV,UNC104,SPG30","biotype":"protein_coding","ncbi_id":"547","summary":"The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]","start":240713764,"end":240820308,"strand":-1,"description":"kinesin family member 1A [Source:HGNC Symbol;Acc:HGNC:888]"}, {"versioned_ensembl_gene_id":"ENSG00000157379.13","gene_symbol":"DHRS1","gene_name":"dehydrogenase/reductase 1 [Source:HGNC Symbol;Acc:HGNC:16445]","synonyms":"SDR19C1,MGC20204,FLJ25430","biotype":"protein_coding","ncbi_id":"115817","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family. The encoded enzyme contains a conserved catalytic domain and likely functions as an oxidoreductase. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2008]","start":24290598,"end":24299833,"strand":-1,"description":"dehydrogenase/reductase 1 [Source:HGNC Symbol;Acc:HGNC:16445]"}, {"versioned_ensembl_gene_id":"ENSG00000227274.1","gene_symbol":"AC005358.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12671862,"end":12706135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282783.1","gene_symbol":"IGHV3-41","gene_name":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28428","summary":null,"start":106467814,"end":106468265,"strand":-1,"description":"immunoglobulin heavy variable 3-41 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5602]"}, {"versioned_ensembl_gene_id":"ENSG00000274587.5","gene_symbol":"LILRB3","gene_name":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]","synonyms":"LIR-3,ILT5,PIRB,HL9,PIR-B,CD85a,LIR3","biotype":"protein_coding","ncbi_id":"11025","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54217271,"end":54223706,"strand":-1,"description":"leukocyte immunoglobulin like receptor B3 [Source:HGNC Symbol;Acc:HGNC:6607]"}, {"versioned_ensembl_gene_id":"ENSG00000231990.1","gene_symbol":"AL442224.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93857083,"end":93858333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147573.16","gene_symbol":"TRIM55","gene_name":"tripartite motif containing 55 [Source:HGNC Symbol;Acc:HGNC:14215]","synonyms":"RNF29,MURF-2","biotype":"protein_coding","ncbi_id":"84675","summary":"The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This protein associates transiently with microtubules, myosin, and titin during muscle sarcomere assembly. It may act as a transient adaptor and plays a regulatory role in the assembly of sarcomeres. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":66126896,"end":66175487,"strand":1,"description":"tripartite motif containing 55 [Source:HGNC Symbol;Acc:HGNC:14215]"}, {"versioned_ensembl_gene_id":"ENSG00000170627.10","gene_symbol":"GTSF1","gene_name":"gametocyte specific factor 1 [Source:HGNC Symbol;Acc:HGNC:26565]","synonyms":"FLJ32942,FAM112B","biotype":"protein_coding","ncbi_id":"121355","summary":null,"start":54455950,"end":54473602,"strand":-1,"description":"gametocyte specific factor 1 [Source:HGNC Symbol;Acc:HGNC:26565]"}, {"versioned_ensembl_gene_id":"ENSG00000235582.2","gene_symbol":"AL365258.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197735636,"end":197736107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250903.8","gene_symbol":"GMDS-AS1","gene_name":"GMDS antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48993]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100508120","summary":null,"start":2245748,"end":2482022,"strand":1,"description":"GMDS antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48993]"}, {"versioned_ensembl_gene_id":"ENSG00000272465.1","gene_symbol":"AL031768.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2437549,"end":2438249,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229194.7","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29787918,"end":29794690,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000277926.4","gene_symbol":"NEU4","gene_name":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]","synonyms":null,"biotype":"protein_coding","ncbi_id":"129807","summary":"The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2009]","start":241808825,"end":241817413,"strand":1,"description":"neuraminidase 4 [Source:HGNC Symbol;Acc:HGNC:21328]"}, {"versioned_ensembl_gene_id":"ENSG00000229131.1","gene_symbol":"AC016710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139469775,"end":139477747,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232908.3","gene_symbol":"HSD17B7P1","gene_name":"hydroxysteroid 17-beta dehydrogenase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18689]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"148818","summary":null,"start":247827486,"end":247828502,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18689]"}, {"versioned_ensembl_gene_id":"ENSG00000255967.1","gene_symbol":"HADHAP2","gene_name":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38585]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399994","summary":null,"start":8634367,"end":8637608,"strand":1,"description":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38585]"}, {"versioned_ensembl_gene_id":"ENSG00000227144.8","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"G7c,C6orf27,NG37","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31752967,"end":31764655,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000180770.3","gene_symbol":"OR7E129P","gene_name":"olfactory receptor family 7 subfamily E member 129 pseudogene [Source:HGNC Symbol;Acc:HGNC:15052]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"391576","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":130021553,"end":130022520,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 129 pseudogene [Source:HGNC Symbol;Acc:HGNC:15052]"}, {"versioned_ensembl_gene_id":"ENSG00000249869.1","gene_symbol":"AC083906.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130013182,"end":130013541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284731.1","gene_symbol":"AC083906.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130002789,"end":130003007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204086.4","gene_symbol":"RPA4","gene_name":"replication protein A4 [Source:HGNC Symbol;Acc:HGNC:30305]","synonyms":"HSU24186","biotype":"protein_coding","ncbi_id":"29935","summary":"This gene encodes a single-stranded DNA-binding protein that is the 30-kDa subunit of the replication protein A complex. Replication protein A is an essential factor for DNA double-strand break repair and cell cycle checkpoint activation. The encoded protein localizes to DNA repair foci and may be involved in the cellular DNA damage response. This protein may also play a role in inhibiting viral replication.[provided by RefSeq, Apr 2010]","start":96883908,"end":96885467,"strand":1,"description":"replication protein A4 [Source:HGNC Symbol;Acc:HGNC:30305]"}, {"versioned_ensembl_gene_id":"ENSG00000125815.8","gene_symbol":"CST8","gene_name":"cystatin 8 [Source:HGNC Symbol;Acc:HGNC:2480]","synonyms":"CTES5,CRES","biotype":"protein_coding","ncbi_id":"10047","summary":"The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes a protein similar to type 2 cystatins. The encoded protein exhibits highly tissue-specific expression in the reproductive tract, suggesting implicit roles in reproduction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":23491101,"end":23496018,"strand":1,"description":"cystatin 8 [Source:HGNC Symbol;Acc:HGNC:2480]"}, {"versioned_ensembl_gene_id":"ENSG00000224184.5","gene_symbol":"MIR3681HG","gene_name":"MIR3681 host gene [Source:HGNC Symbol;Acc:HGNC:52001]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506457","summary":null,"start":11848622,"end":12578348,"strand":1,"description":"MIR3681 host gene [Source:HGNC Symbol;Acc:HGNC:52001]"}, {"versioned_ensembl_gene_id":"ENSG00000084073.8","gene_symbol":"ZMPSTE24","gene_name":"zinc metallopeptidase STE24 [Source:HGNC Symbol;Acc:HGNC:12877]","synonyms":"Ste24p,STE24,PRO1,HGPS,FACE-1","biotype":"protein_coding","ncbi_id":"10269","summary":"This gene encodes a member of the peptidase M48A family. The encoded protein is a zinc metalloproteinase involved in the two step post-translational proteolytic cleavage of carboxy terminal residues of farnesylated prelamin A to form mature lamin A. Mutations in this gene have been associated with mandibuloacral dysplasia and restrictive dermopathy. [provided by RefSeq, Jul 2008]","start":40258107,"end":40294184,"strand":1,"description":"zinc metallopeptidase STE24 [Source:HGNC Symbol;Acc:HGNC:12877]"}, {"versioned_ensembl_gene_id":"ENSG00000229976.1","gene_symbol":"AL118523.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39785721,"end":39813229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120137.6","gene_symbol":"PANK3","gene_name":"pantothenate kinase 3 [Source:HGNC Symbol;Acc:HGNC:19365]","synonyms":"FLJ12899","biotype":"protein_coding","ncbi_id":"79646","summary":"This gene encodes a protein belonging to the pantothenate kinase family. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by CoA. This family member is expressed most abundantly in the liver. [provided by RefSeq, Jul 2008]","start":168548495,"end":168579600,"strand":-1,"description":"pantothenate kinase 3 [Source:HGNC Symbol;Acc:HGNC:19365]"}, {"versioned_ensembl_gene_id":"ENSG00000188573.7","gene_symbol":"FBLL1","gene_name":"fibrillarin like 1 [Source:HGNC Symbol;Acc:HGNC:35458]","synonyms":"LOC345630","biotype":"protein_coding","ncbi_id":"345630","summary":null,"start":168529116,"end":168530634,"strand":1,"description":"fibrillarin like 1 [Source:HGNC Symbol;Acc:HGNC:35458]"}, {"versioned_ensembl_gene_id":"ENSG00000228491.2","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29738863,"end":29746102,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000279746.1","gene_symbol":"AC092850.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131295522,"end":131298218,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188690.12","gene_symbol":"UROS","gene_name":"uroporphyrinogen III synthase [Source:HGNC Symbol;Acc:HGNC:12592]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7390","summary":"The protein encoded by this gene catalyzes the fourth step of porphyrin biosynthesis in the heme biosynthetic pathway. Defects in this gene cause congenital erythropoietic porphyria (Gunther's disease). [provided by RefSeq, Jul 2008]","start":125784980,"end":125823248,"strand":-1,"description":"uroporphyrinogen III synthase [Source:HGNC Symbol;Acc:HGNC:12592]"}, {"versioned_ensembl_gene_id":"ENSG00000282389.1","gene_symbol":"AC131056.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":36161606,"end":36162932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225739.1","gene_symbol":"NPM1P18","gene_name":"nucleophosmin 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:7920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"10829","summary":null,"start":36818959,"end":36819690,"strand":1,"description":"nucleophosmin 1 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:7920]"}, {"versioned_ensembl_gene_id":"ENSG00000259846.1","gene_symbol":"AC092131.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64364781,"end":64600247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231606.1","gene_symbol":"AL357873.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14221891,"end":14223118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187862.11","gene_symbol":"TTC24","gene_name":"tetratricopeptide repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:32348]","synonyms":null,"biotype":"protein_coding","ncbi_id":"164118","summary":null,"start":156579727,"end":156586770,"strand":1,"description":"tetratricopeptide repeat domain 24 [Source:HGNC Symbol;Acc:HGNC:32348]"}, {"versioned_ensembl_gene_id":"ENSG00000240912.1","gene_symbol":"AC092896.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114103249,"end":114103628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232233.1","gene_symbol":"LINC02043","gene_name":"long intergenic non-protein coding RNA 2043 [Source:HGNC Symbol;Acc:HGNC:52883]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724699","summary":null,"start":186810880,"end":186825521,"strand":-1,"description":"long intergenic non-protein coding RNA 2043 [Source:HGNC Symbol;Acc:HGNC:52883]"}, {"versioned_ensembl_gene_id":"ENSG00000179406.7","gene_symbol":"LINC00174","gene_name":"long intergenic non-protein coding RNA 174 [Source:HGNC Symbol;Acc:HGNC:27788]","synonyms":"NCRNA00174","biotype":"processed_transcript","ncbi_id":"285908","summary":null,"start":66376044,"end":66493566,"strand":-1,"description":"long intergenic non-protein coding RNA 174 [Source:HGNC Symbol;Acc:HGNC:27788]"}, {"versioned_ensembl_gene_id":"ENSG00000237901.1","gene_symbol":"AC009161.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62357371,"end":62357746,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000089050.15","gene_symbol":"RBBP9","gene_name":"RB binding protein 9, serine hydrolase [Source:HGNC Symbol;Acc:HGNC:9892]","synonyms":"Bog","biotype":"protein_coding","ncbi_id":"10741","summary":"The protein encoded by this gene is a retinoblastoma binding protein that may play a role in the regulation of cell proliferation and differentiation. Two alternatively spliced transcript variants of this gene with identical predicted protein products have been reported, one of which is a nonsense-mediated decay candidate. [provided by RefSeq, Jul 2008]","start":18486540,"end":18497243,"strand":-1,"description":"RB binding protein 9, serine hydrolase [Source:HGNC Symbol;Acc:HGNC:9892]"}, {"versioned_ensembl_gene_id":"ENSG00000228538.5","gene_symbol":"AC009411.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21638431,"end":21649563,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253190.3","gene_symbol":"AC084082.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66112667,"end":66115207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267793.1","gene_symbol":"AC009977.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":19598188,"end":19598757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254550.1","gene_symbol":"OMP","gene_name":"olfactory marker protein [Source:HGNC Symbol;Acc:HGNC:8136]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4975","summary":" Olfactory marker protein is uniquely associated with the mature olfactory receptor neurons in many vertebrate species from fish to man. The OMP gene structure and protein sequence are highly conserved between mouse, rat and human. Results of the mouse knockout studies show that OMP-null mice are compromised in their ability to respond to odor stimuli, and that OMP represents a novel modulatory component of the odor detection/signal transduction cascade. [provided by RefSeq, Jul 2008]","start":77102840,"end":77103331,"strand":1,"description":"olfactory marker protein [Source:HGNC Symbol;Acc:HGNC:8136]"}, {"versioned_ensembl_gene_id":"ENSG00000224360.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bPG70P20.2,TIGD1L,bCX111D4.7,bQB10J12.1","biotype":"processed_transcript","ncbi_id":"414771","summary":null,"start":30856848,"end":30865810,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000253357.1","gene_symbol":"AC008708.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":167721363,"end":167729124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261622.1","gene_symbol":"AC021439.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23912409,"end":23941716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225788.1","gene_symbol":"BX664702.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":33061015,"end":33061529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253191.1","gene_symbol":"IGKV1D-32","gene_name":"immunoglobulin kappa variable 1D-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5752]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28897","summary":null,"start":89928422,"end":89928867,"strand":1,"description":"immunoglobulin kappa variable 1D-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5752]"}, {"versioned_ensembl_gene_id":"ENSG00000130783.13","gene_symbol":"CCDC62","gene_name":"coiled-coil domain containing 62 [Source:HGNC Symbol;Acc:HGNC:30723]","synonyms":"TSP-NY,FLJ40344,ERAP75,CT109","biotype":"protein_coding","ncbi_id":"84660","summary":null,"start":122774327,"end":122827528,"strand":1,"description":"coiled-coil domain containing 62 [Source:HGNC Symbol;Acc:HGNC:30723]"}, {"versioned_ensembl_gene_id":"ENSG00000143919.14","gene_symbol":"CAMKMT","gene_name":"calmodulin-lysine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:26276]","synonyms":"CLNMT,C2orf34","biotype":"protein_coding","ncbi_id":"79823","summary":"This gene encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. The protein contains a AdoMet-binding motif and may play a role in calcium-dependent signaling. [provided by RefSeq, Sep 2012]","start":44361950,"end":44772592,"strand":1,"description":"calmodulin-lysine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:26276]"}, {"versioned_ensembl_gene_id":"ENSG00000271646.1","gene_symbol":"AC099343.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":184474802,"end":184477304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265480.5","gene_symbol":"KRT18P55","gene_name":"keratin 18 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:26874]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284085","summary":null,"start":28275986,"end":28317783,"strand":-1,"description":"keratin 18 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:26874]"}, {"versioned_ensembl_gene_id":"ENSG00000223368.2","gene_symbol":"AL513124.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73870896,"end":73873297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005302.17","gene_symbol":"MSL3","gene_name":"MSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7370]","synonyms":"MSL3L1","biotype":"protein_coding","ncbi_id":"10943","summary":"This gene encodes a nuclear protein that is similar to the product of the Drosophila male-specific lethal-3 gene. The Drosophila protein plays a critical role in a dosage-compensation pathway, which equalizes X-linked gene expression in males and females. Thus, the human protein is thought to play a similar function in chromatin remodeling and transcriptional regulation, and it has been found as part of a complex that is responsible for histone H4 lysine-16 acetylation. This gene can undergo X inactivation. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2, 7 and 8. [provided by RefSeq, Jul 2010]","start":11758159,"end":11775753,"strand":1,"description":"MSL complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:7370]"}, {"versioned_ensembl_gene_id":"ENSG00000280109.2","gene_symbol":"PLAC4","gene_name":"placenta specific 4 [Source:HGNC Symbol;Acc:HGNC:14616]","synonyms":"MGC126666,MGC126664,C21orf115,PRED78","biotype":"protein_coding","ncbi_id":"191585","summary":null,"start":41175231,"end":41180818,"strand":-1,"description":"placenta specific 4 [Source:HGNC Symbol;Acc:HGNC:14616]"}, {"versioned_ensembl_gene_id":"ENSG00000237080.2","gene_symbol":"EHMT2-AS1","gene_name":"EHMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39751]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478954","summary":null,"start":31883761,"end":31884204,"strand":1,"description":"EHMT2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39751]"}, {"versioned_ensembl_gene_id":"ENSG00000237903.1","gene_symbol":"AC004000.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":119422917,"end":119423547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283128.1","gene_symbol":"AC009403.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":155474256,"end":155644406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232829.3","gene_symbol":"GSTO3P","gene_name":"glutathione S-transferase omega 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:23065]","synonyms":"GSTO3P1","biotype":"processed_pseudogene","ncbi_id":"344813","summary":null,"start":130827659,"end":130828376,"strand":1,"description":"glutathione S-transferase omega 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:23065]"}, {"versioned_ensembl_gene_id":"ENSG00000165238.16","gene_symbol":"WNK2","gene_name":"WNK lysine deficient protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:14542]","synonyms":"NY-CO-43,KIAA1760,SDCCAG43,PRKWNK2","biotype":"protein_coding","ncbi_id":"65268","summary":"The protein encoded by this gene is a cytoplasmic serine-threonine kinase that belongs to the protein kinase superfamily. The protein plays an important role in the regulation of electrolyte homeostasis, cell signaling survival, and proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":93184916,"end":93320572,"strand":1,"description":"WNK lysine deficient protein kinase 2 [Source:HGNC Symbol;Acc:HGNC:14542]"}, {"versioned_ensembl_gene_id":"ENSG00000146910.12","gene_symbol":"CNPY1","gene_name":"canopy FGF signaling regulator 1 [Source:HGNC Symbol;Acc:HGNC:27786]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285888","summary":"Cnpy1 is expressed in the midbrain-hindbrain (MHB) boundary in zebrafish, binds FGFR1 (MIM 136350), and plays a role in FGF signaling (Hirate and Okamoto, 2006 [PubMed 16488878]).[supplied by OMIM, Dec 2008]","start":155474206,"end":155555450,"strand":-1,"description":"canopy FGF signaling regulator 1 [Source:HGNC Symbol;Acc:HGNC:27786]"}, {"versioned_ensembl_gene_id":"ENSG00000122729.18","gene_symbol":"ACO1","gene_name":"aconitase 1 [Source:HGNC Symbol;Acc:HGNC:117]","synonyms":"IRP1,IREBP,IREB1","biotype":"protein_coding","ncbi_id":"48","summary":"The protein encoded by this gene is a bifunctional, cytosolic protein that functions as an essential enzyme in the TCA cycle and interacts with mRNA to control the levels of iron inside cells. When cellular iron levels are high, this protein binds to a 4Fe-4S cluster and functions as an aconitase. Aconitases are iron-sulfur proteins that function to catalyze the conversion of citrate to isocitrate. When cellular iron levels are low, the protein binds to iron-responsive elements (IREs), which are stem-loop structures found in the 5' UTR of ferritin mRNA, and in the 3' UTR of transferrin receptor mRNA. When the protein binds to IRE, it results in repression of translation of ferritin mRNA, and inhibition of degradation of the otherwise rapidly degraded transferrin receptor mRNA. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alternative splicing results in multiple transcript variants [provided by RefSeq, Jan 2014]","start":32384603,"end":32454769,"strand":1,"description":"aconitase 1 [Source:HGNC Symbol;Acc:HGNC:117]"}, {"versioned_ensembl_gene_id":"ENSG00000240873.1","gene_symbol":"RPS29P22","gene_name":"ribosomal protein S29 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271384","summary":null,"start":28116239,"end":28116406,"strand":-1,"description":"ribosomal protein S29 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35799]"}, {"versioned_ensembl_gene_id":"ENSG00000243679.1","gene_symbol":"AC018638.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128653969,"end":128654722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230715.3","gene_symbol":"AC018638.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128652841,"end":128653243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227304.3","gene_symbol":"AC067942.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":82494786,"end":82496278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234588.1","gene_symbol":"FABP5P14","gene_name":"fatty acid binding protein 5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:31065]","synonyms":"FABP5L14","biotype":"processed_pseudogene","ncbi_id":"100873957","summary":null,"start":216805737,"end":216806129,"strand":-1,"description":"fatty acid binding protein 5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:31065]"}, {"versioned_ensembl_gene_id":"ENSG00000255374.3","gene_symbol":"TAS2R43","gene_name":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]","synonyms":"T2R52","biotype":"protein_coding","ncbi_id":"259289","summary":"TAS2R43 belongs to the large TAS2R receptor family. TAS2Rs are expressed on the surface of taste receptor cells and mediate the perception of bitterness through a G protein-coupled second messenger pathway (Conte et al., 2002 [PubMed 12584440]). For further information on TAS2Rs, see MIM 604791.[supplied by OMIM, Mar 2009]","start":11091287,"end":11092313,"strand":-1,"description":"taste 2 receptor member 43 [Source:HGNC Symbol;Acc:HGNC:18875]"}, {"versioned_ensembl_gene_id":"ENSG00000155495.8","gene_symbol":"MAGEC1","gene_name":"MAGE family member C1 [Source:HGNC Symbol;Acc:HGNC:6812]","synonyms":"MGC39366,MAGE-C1,CT7.1,CT7","biotype":"protein_coding","ncbi_id":"9947","summary":"This gene is a member of the melanoma antigen gene (MAGE) family. The proteins of this family are tumor-specific antigens that can be recognized by autologous cytolytic T lymphocytes. This protein contains a large number of unique short repetitive sequences in front of the MAGE-homologous sequence, and therefore is about 800 aa longer than the other MAGE proteins. [provided by RefSeq, Jul 2008]","start":141903894,"end":141909388,"strand":1,"description":"MAGE family member C1 [Source:HGNC Symbol;Acc:HGNC:6812]"}, {"versioned_ensembl_gene_id":"ENSG00000256589.2","gene_symbol":"ENPP7P5","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48688]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480674","summary":null,"start":8254527,"end":8308855,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48688]"}, {"versioned_ensembl_gene_id":"ENSG00000256682.2","gene_symbol":"AC006518.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":10894943,"end":10896952,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277952.1","gene_symbol":"AC092745.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8340182,"end":8340397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230471.1","gene_symbol":"AP000532.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15600908,"end":15604882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231857.1","gene_symbol":"MORF4L1P5","gene_name":"mortality factor 4 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35425]","synonyms":"MORF4LP5","biotype":"processed_pseudogene","ncbi_id":"100129288","summary":null,"start":65327988,"end":65331233,"strand":-1,"description":"mortality factor 4 like 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35425]"}, {"versioned_ensembl_gene_id":"ENSG00000242802.6","gene_symbol":"AP5Z1","gene_name":"adaptor related protein complex 5 zeta 1 subunit [Source:HGNC Symbol;Acc:HGNC:22197]","synonyms":"zeta,SPG48,KIAA0415","biotype":"protein_coding","ncbi_id":"9907","summary":"This gene was identified by genome-wide screen for genes involved in homologous recombination DNA double-strand break repair (HR-DSBR). The encoded protein was found in a complex with other proteins that have a role in HR-DSBR. Knockdown of this gene reduced homologous recombination, and mutations in this gene were found in patients with spastic paraplegia. It was concluded that this gene likely encodes a helicase (PMID:20613862). [provided by RefSeq, Jan 2011]","start":4775622,"end":4794312,"strand":1,"description":"adaptor related protein complex 5 zeta 1 subunit [Source:HGNC Symbol;Acc:HGNC:22197]"}, {"versioned_ensembl_gene_id":"ENSG00000255437.1","gene_symbol":"AC023538.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14022687,"end":14023422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273827.2","gene_symbol":"OR2T5","gene_name":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401993","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":248494630,"end":248495663,"strand":1,"description":"olfactory receptor family 2 subfamily T member 5 [Source:HGNC Symbol;Acc:HGNC:15017]"}, {"versioned_ensembl_gene_id":"ENSG00000163530.4","gene_symbol":"DPPA2","gene_name":"developmental pluripotency associated 2 [Source:HGNC Symbol;Acc:HGNC:19197]","synonyms":"PESCRG1,CT100","biotype":"protein_coding","ncbi_id":"151871","summary":null,"start":109293788,"end":109316517,"strand":-1,"description":"developmental pluripotency associated 2 [Source:HGNC Symbol;Acc:HGNC:19197]"}, {"versioned_ensembl_gene_id":"ENSG00000101400.5","gene_symbol":"SNTA1","gene_name":"syntrophin alpha 1 [Source:HGNC Symbol;Acc:HGNC:11167]","synonyms":"TACIP1,SNT1,LQT12","biotype":"protein_coding","ncbi_id":"6640","summary":"Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS). This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue. [provided by RefSeq, Jan 2013]","start":33407955,"end":33443892,"strand":-1,"description":"syntrophin alpha 1 [Source:HGNC Symbol;Acc:HGNC:11167]"}, {"versioned_ensembl_gene_id":"ENSG00000261809.1","gene_symbol":"CYP3A54P","gene_name":"cytochrome P450 family 3 subfamily A member 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:42413]","synonyms":"CYP3A-se1[2]","biotype":"processed_pseudogene","ncbi_id":"106480749","summary":null,"start":4511959,"end":4512033,"strand":-1,"description":"cytochrome P450 family 3 subfamily A member 54, pseudogene [Source:HGNC Symbol;Acc:HGNC:42413]"}, {"versioned_ensembl_gene_id":"ENSG00000230037.1","gene_symbol":"UBBP1","gene_name":"ubiquitin B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12464]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"7315","summary":null,"start":136329441,"end":136329913,"strand":-1,"description":"ubiquitin B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12464]"}, {"versioned_ensembl_gene_id":"ENSG00000262899.1","gene_symbol":"AC004232.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3307573,"end":3308393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267705.1","gene_symbol":"AC104365.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58752179,"end":58753898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204252.13","gene_symbol":"HLA-DOA","gene_name":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]","synonyms":"HLA-D0-alpha,HLA-DZA,HLA-DNA","biotype":"protein_coding","ncbi_id":"3111","summary":"HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008]","start":33004178,"end":33009612,"strand":-1,"description":"major histocompatibility complex, class II, DO alpha [Source:HGNC Symbol;Acc:HGNC:4936]"}, {"versioned_ensembl_gene_id":"ENSG00000269890.1","gene_symbol":"AL353593.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":228270443,"end":228274397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234164.2","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206,HLA-DR1BL,D6S206E,HLA-DRB1L","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32498480,"end":32512136,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000238056.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32215364,"end":32221379,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000236281.1","gene_symbol":"NDUFB9P2","gene_name":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52270]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128596","summary":null,"start":131753746,"end":131754252,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52270]"}, {"versioned_ensembl_gene_id":"ENSG00000227864.1","gene_symbol":"ARL5AP1","gene_name":"ADP ribosylation factor like GTPase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641382","summary":null,"start":119186442,"end":119186829,"strand":-1,"description":"ADP ribosylation factor like GTPase 5A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43933]"}, {"versioned_ensembl_gene_id":"ENSG00000226472.8","gene_symbol":"AC008013.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30978308,"end":31006010,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212643.2","gene_symbol":"ZRSR1","gene_name":"zinc finger CCCH-type, RNA binding motif and serine/arginine rich 1 [Source:HGNC Symbol;Acc:HGNC:12456]","synonyms":"ZC3H21,U2AFBPL,U2AF1RS1,U2AF1P,U2AF1L1,U2AF1-RS1","biotype":"protein_coding","ncbi_id":"7310","summary":null,"start":112891422,"end":112893094,"strand":1,"description":"zinc finger CCCH-type, RNA binding motif and serine/arginine rich 1 [Source:HGNC Symbol;Acc:HGNC:12456]"}, {"versioned_ensembl_gene_id":"ENSG00000270823.1","gene_symbol":"AC007938.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130495794,"end":130498427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143869.6","gene_symbol":"GDF7","gene_name":"growth differentiation factor 7 [Source:HGNC Symbol;Acc:HGNC:4222]","synonyms":"BMP12","biotype":"protein_coding","ncbi_id":"151449","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein may play a role in the differentiation of tendon cells and spinal cord interneurons. A mutation in this gene may be associated with increased risk for Barrett's esophagus and esophageal adenocarcinoma. [provided by RefSeq, Sep 2016]","start":20666664,"end":20679245,"strand":1,"description":"growth differentiation factor 7 [Source:HGNC Symbol;Acc:HGNC:4222]"}, {"versioned_ensembl_gene_id":"ENSG00000205537.2","gene_symbol":"AC121338.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47882649,"end":47901525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120686.11","gene_symbol":"UFM1","gene_name":"ubiquitin fold modifier 1 [Source:HGNC Symbol;Acc:HGNC:20597]","synonyms":"C13orf20,bA131P10.1","biotype":"protein_coding","ncbi_id":"51569","summary":"UFM1 is a ubiquitin-like protein that is conjugated to target proteins by E1-like activating enzyme UBA5 (UBE1DC1; MIM 610552) and E2-like conjugating enzyme UFC1 (MIM 610554) in a manner analogous to ubiquitylation (see UBE2M; MIM 603173) (Komatsu et al., 2004 [PubMed 15071506]).[supplied by OMIM, Dec 2008]","start":38349849,"end":38363619,"strand":1,"description":"ubiquitin fold modifier 1 [Source:HGNC Symbol;Acc:HGNC:20597]"}, {"versioned_ensembl_gene_id":"ENSG00000226045.1","gene_symbol":"AC234644.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130645225,"end":130645594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198901.13","gene_symbol":"PRC1","gene_name":"protein regulator of cytokinesis 1 [Source:HGNC Symbol;Acc:HGNC:9341]","synonyms":"ASE1","biotype":"protein_coding","ncbi_id":"9055","summary":"This gene encodes a protein that is involved in cytokinesis. The protein is present at high levels during the S and G2/M phases of mitosis but its levels drop dramatically when the cell exits mitosis and enters the G1 phase. It is located in the nucleus during interphase, becomes associated with mitotic spindles in a highly dynamic manner during mitosis, and localizes to the cell mid-body during cytokinesis. This protein has been shown to be a substrate of several cyclin-dependent kinases (CDKs). It is necessary for polarizing parallel microtubules and concentrating the factors responsible for contractile ring assembly. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":90966038,"end":90995629,"strand":-1,"description":"protein regulator of cytokinesis 1 [Source:HGNC Symbol;Acc:HGNC:9341]"}, {"versioned_ensembl_gene_id":"ENSG00000244052.1","gene_symbol":"RPL5P24","gene_name":"ribosomal protein L5 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35828]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270841","summary":null,"start":102923371,"end":102924255,"strand":-1,"description":"ribosomal protein L5 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35828]"}, {"versioned_ensembl_gene_id":"ENSG00000241926.1","gene_symbol":"MTCO1P55","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:52120]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075179","summary":null,"start":141801315,"end":141802059,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:52120]"}, {"versioned_ensembl_gene_id":"ENSG00000275332.1","gene_symbol":"AC103691.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64943240,"end":64943672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269680.1","gene_symbol":"AC008760.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6748293,"end":6751467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152969.18","gene_symbol":"JAKMIP1","gene_name":"janus kinase and microtubule interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26460]","synonyms":"MARLIN1,JAMIP1,Gababrbp,FLJ31564","biotype":"protein_coding","ncbi_id":"152789","summary":null,"start":6026199,"end":6200591,"strand":-1,"description":"janus kinase and microtubule interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:26460]"}, {"versioned_ensembl_gene_id":"ENSG00000280991.1","gene_symbol":"AL121956.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":166229334,"end":166229554,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273907.1","gene_symbol":"CA15P2","gene_name":"carbonic anhydrase 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14916]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440795","summary":null,"start":18636445,"end":18638405,"strand":-1,"description":"carbonic anhydrase 15 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14916]"}, {"versioned_ensembl_gene_id":"ENSG00000275428.2","gene_symbol":"AC024940.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":31111652,"end":31208427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257438.1","gene_symbol":"AC011595.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106103163,"end":106106165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250894.1","gene_symbol":"PRAMEF31P","gene_name":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129611","summary":null,"start":13245863,"end":13248652,"strand":1,"description":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]"}, {"versioned_ensembl_gene_id":"ENSG00000255823.4","gene_symbol":"MTRNR2L8","gene_name":"MT-RNR2-like 8 [Source:HGNC Symbol;Acc:HGNC:37165]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463486","summary":null,"start":10507887,"end":10509189,"strand":-1,"description":"MT-RNR2-like 8 [Source:HGNC Symbol;Acc:HGNC:37165]"}, {"versioned_ensembl_gene_id":"ENSG00000244753.2","gene_symbol":"RPL15P21","gene_name":"ribosomal protein L15 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36190]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132722","summary":null,"start":10860535,"end":10861462,"strand":-1,"description":"ribosomal protein L15 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:36190]"}, {"versioned_ensembl_gene_id":"ENSG00000187553.8","gene_symbol":"CYP26C1","gene_name":"cytochrome P450 family 26 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:20577]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340665","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is involved in the catabolism of all-trans- and 9-cis-retinoic acid, and thus contributes to the regulation of retinoic acid levels in cells and tissues. This gene is adjacent to a related gene on chromosome 10q23.33. [provided by RefSeq, Jul 2008]","start":93060808,"end":93069536,"strand":1,"description":"cytochrome P450 family 26 subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:20577]"}, {"versioned_ensembl_gene_id":"ENSG00000204505.4","gene_symbol":"PRAMEF9","gene_name":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343070","summary":null,"start":13172455,"end":13179464,"strand":1,"description":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]"}, {"versioned_ensembl_gene_id":"ENSG00000147753.9","gene_symbol":"TTTY7","gene_name":"testis-specific transcript, Y-linked 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18488]","synonyms":"TTTY7A,LINC00129","biotype":"lincRNA","ncbi_id":"246122","summary":null,"start":6449468,"end":6457906,"strand":1,"description":"testis-specific transcript, Y-linked 7 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18488]"}, {"versioned_ensembl_gene_id":"ENSG00000236378.1","gene_symbol":"AL133319.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135807148,"end":135808466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173207.12","gene_symbol":"CKS1B","gene_name":"CDC28 protein kinase regulatory subunit 1B [Source:HGNC Symbol;Acc:HGNC:19083]","synonyms":"ckshs1,CKS1","biotype":"protein_coding","ncbi_id":"1163","summary":"CKS1B protein binds to the catalytic subunit of the cyclin dependent kinases and is essential for their biological function. The CKS1B mRNA is found to be expressed in different patterns through the cell cycle in HeLa cells, which reflects a specialized role for the encoded protein. At least two transcript variants have been identified for this gene, and it appears that only one of them encodes a protein. [provided by RefSeq, Sep 2008]","start":154974653,"end":154979249,"strand":1,"description":"CDC28 protein kinase regulatory subunit 1B [Source:HGNC Symbol;Acc:HGNC:19083]"}, {"versioned_ensembl_gene_id":"ENSG00000168746.8","gene_symbol":"LINC01620","gene_name":"long intergenic non-protein coding RNA 1620 [Source:HGNC Symbol;Acc:HGNC:16195]","synonyms":"dJ1013A22.3,C20orf62","biotype":"lincRNA","ncbi_id":"140834","summary":null,"start":44436172,"end":44465349,"strand":-1,"description":"long intergenic non-protein coding RNA 1620 [Source:HGNC Symbol;Acc:HGNC:16195]"}, {"versioned_ensembl_gene_id":"ENSG00000177721.4","gene_symbol":"ANXA2R","gene_name":"annexin A2 receptor [Source:HGNC Symbol;Acc:HGNC:33463]","synonyms":"C5orf39,AXIIR","biotype":"protein_coding","ncbi_id":"389289","summary":null,"start":43039081,"end":43043170,"strand":-1,"description":"annexin A2 receptor [Source:HGNC Symbol;Acc:HGNC:33463]"}, {"versioned_ensembl_gene_id":"ENSG00000232385.2","gene_symbol":"RPS3AP25","gene_name":"ribosomal protein S3a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645968","summary":null,"start":94695027,"end":94695819,"strand":-1,"description":"ribosomal protein S3a pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:36801]"}, {"versioned_ensembl_gene_id":"ENSG00000279542.1","gene_symbol":"AC015908.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10821901,"end":10822243,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272144.1","gene_symbol":"AC025171.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43061395,"end":43062441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233755.1","gene_symbol":"AL050344.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25043707,"end":25113120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164458.9","gene_symbol":"T","gene_name":"T brachyury transcription factor [Source:HGNC Symbol;Acc:HGNC:11515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6862","summary":"The protein encoded by this gene is an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Variation in this gene was associated with susceptibility to neural tube defects and chordoma. A mutation in this gene was found in a family with sacral agenesis with vertebral anomalies. [provided by RefSeq, Sep 2018]","start":166157656,"end":166168700,"strand":-1,"description":"T brachyury transcription factor [Source:HGNC Symbol;Acc:HGNC:11515]"}, {"versioned_ensembl_gene_id":"ENSG00000261025.1","gene_symbol":"AL445471.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24968423,"end":24970865,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276929.1","gene_symbol":"AL590240.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55137930,"end":55142433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278487.1","gene_symbol":"AC106800.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43143362,"end":43143514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270493.1","gene_symbol":"AL670379.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120937762,"end":120938015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233601.1","gene_symbol":"NCOR1P3","gene_name":"nuclear receptor corepressor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42996]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874183","summary":null,"start":57599794,"end":57610104,"strand":1,"description":"nuclear receptor corepressor 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42996]"}, {"versioned_ensembl_gene_id":"ENSG00000278319.1","gene_symbol":"AL590240.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55101637,"end":55102026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256346.1","gene_symbol":"AC092470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14169746,"end":14169877,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152795.17","gene_symbol":"HNRNPDL","gene_name":"heterogeneous nuclear ribonucleoprotein D like [Source:HGNC Symbol;Acc:HGNC:5037]","synonyms":"laAUF1,JKTBP,HNRPDL","biotype":"protein_coding","ncbi_id":"9987","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two RRM domains that bind to RNAs. Three alternatively spliced transcript variants have been described for this gene. One of the variants is probably not translated because the transcript is a candidate for nonsense-mediated mRNA decay. The protein isoforms encoded by this gene are similar to its family member HNRPD. [provided by RefSeq, May 2011]","start":82422564,"end":82430408,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein D like [Source:HGNC Symbol;Acc:HGNC:5037]"}, {"versioned_ensembl_gene_id":"ENSG00000211451.12","gene_symbol":"GNRHR2","gene_name":"gonadotropin releasing hormone receptor 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16341]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"114814","summary":"In non-hominoid primates and non-mammalian vertebrates, the gonadotropin releasing hormone 2 receptor gene (GnRHR2) encodes a seven-transmembrane G-protein coupled receptor. However, in human, the corresponding reading frame contains a premature stop codon, which has been suggested to encode a selenocysteine residue, but there is no solid evidence for selenocysteine incorporation (PMID: 12538601). It appears that the human GnRHR2 transcription occurs but the gene does not likely produce a functional multi-transmembrane protein. A non-transcribed pseudogene of GnRHR2 is located on chromosome 14. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2013]","start":145919013,"end":145925341,"strand":1,"description":"gonadotropin releasing hormone receptor 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16341]"}, {"versioned_ensembl_gene_id":"ENSG00000103472.10","gene_symbol":"RRN3P2","gene_name":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37619]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"653390","summary":null,"start":29074976,"end":29116718,"strand":1,"description":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37619]"}, {"versioned_ensembl_gene_id":"ENSG00000280778.1","gene_symbol":"AC243547.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":145927258,"end":145977811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236446.3","gene_symbol":"CT47B1","gene_name":"cancer/testis antigen family 47, member B1 [Source:HGNC Symbol;Acc:HGNC:33293]","synonyms":"CT47.13","biotype":"protein_coding","ncbi_id":"643311","summary":null,"start":120872603,"end":120875929,"strand":-1,"description":"cancer/testis antigen family 47, member B1 [Source:HGNC Symbol;Acc:HGNC:33293]"}, {"versioned_ensembl_gene_id":"ENSG00000271117.1","gene_symbol":"AC078841.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36146842,"end":36148024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271202.1","gene_symbol":"PRR13P7","gene_name":"proline rich 13 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289644","summary":null,"start":91909738,"end":91910167,"strand":-1,"description":"proline rich 13 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50620]"}, {"versioned_ensembl_gene_id":"ENSG00000124587.13","gene_symbol":"PEX6","gene_name":"peroxisomal biogenesis factor 6 [Source:HGNC Symbol;Acc:HGNC:8859]","synonyms":"PAF-2,PXAAA1","biotype":"protein_coding","ncbi_id":"5190","summary":"This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":42963870,"end":42979220,"strand":-1,"description":"peroxisomal biogenesis factor 6 [Source:HGNC Symbol;Acc:HGNC:8859]"}, {"versioned_ensembl_gene_id":"ENSG00000125798.14","gene_symbol":"FOXA2","gene_name":"forkhead box A2 [Source:HGNC Symbol;Acc:HGNC:5022]","synonyms":"HNF3B","biotype":"protein_coding","ncbi_id":"3170","summary":"This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific genes such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. This gene has been linked to sporadic cases of maturity-onset diabetes of the young. Transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008]","start":22581005,"end":22585455,"strand":-1,"description":"forkhead box A2 [Source:HGNC Symbol;Acc:HGNC:5022]"}, {"versioned_ensembl_gene_id":"ENSG00000100106.19","gene_symbol":"TRIOBP","gene_name":"TRIO and F-actin binding protein [Source:HGNC Symbol;Acc:HGNC:17009]","synonyms":"KIAA1662,HRIHFB2122,DFNB28,Tara,TAP68","biotype":"protein_coding","ncbi_id":"11078","summary":"This gene encodes a protein with an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. The protein also associates with F-actin and stabilizes F-actin structures. Mutations in this gene have been associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have been found for this gene, however some transcripts may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Nov 2008]","start":37697004,"end":37776556,"strand":1,"description":"TRIO and F-actin binding protein [Source:HGNC Symbol;Acc:HGNC:17009]"}, {"versioned_ensembl_gene_id":"ENSG00000242622.1","gene_symbol":"AC092910.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120094895,"end":120136783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253901.1","gene_symbol":"AC103409.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91542924,"end":91907619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178343.4","gene_symbol":"SHISA3","gene_name":"shisa family member 3 [Source:HGNC Symbol;Acc:HGNC:25159]","synonyms":"hShisa3","biotype":"protein_coding","ncbi_id":"152573","summary":"This gene encodes a single-transmembrane protein which is one of nine members of a family of transmembrane adaptors that modulate both WNT and FGF signaling by blocking the maturation and transport of their receptors to the cell surface. Members of this family contain an N-terminal cysteine-rich domain with a distinct cysteine pattern, a single transmembrane domain, and a C-terminal proline-rich, low complexity region. The encoded protein acts as a tumor suppressor by accelerating beta-catenin degradation. [provided by RefSeq, Jul 2017]","start":42397839,"end":42402487,"strand":1,"description":"shisa family member 3 [Source:HGNC Symbol;Acc:HGNC:25159]"}, {"versioned_ensembl_gene_id":"ENSG00000184647.10","gene_symbol":"PRSS55","gene_name":"protease, serine 55 [Source:HGNC Symbol;Acc:HGNC:30824]","synonyms":"UNQ9391,T-SP1,CT153","biotype":"protein_coding","ncbi_id":"203074","summary":"This gene encodes a member of a group of membrane-anchored chymotrypsin (S1)-like serine proteases. The enocoded protein is primarily expressed in the Leydig and Sertoli cells of the testis and may be involved in male fertility. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]","start":10525546,"end":10554166,"strand":1,"description":"protease, serine 55 [Source:HGNC Symbol;Acc:HGNC:30824]"}, {"versioned_ensembl_gene_id":"ENSG00000225146.1","gene_symbol":"AC073957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1029025,"end":1043891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276999.1","gene_symbol":"AC226770.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21655154,"end":21656539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253186.2","gene_symbol":"AC022616.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43253732,"end":43254089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278601.1","gene_symbol":"AL158163.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":110907483,"end":110908182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224079.1","gene_symbol":"AC091729.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1074450,"end":1078036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283339.1","gene_symbol":"AC093726.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155074599,"end":155074748,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206448.3","gene_symbol":"PPIAP30","gene_name":"peptidylprolyl isomerase A pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:44878]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100192204","summary":null,"start":15154802,"end":15155320,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:44878]"}, {"versioned_ensembl_gene_id":"ENSG00000279486.5","gene_symbol":"OR2AG1","gene_name":"olfactory receptor family 2 subfamily AG member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15142]","synonyms":"OR2AG3","biotype":"protein_coding","ncbi_id":"144125","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":6783020,"end":6791558,"strand":1,"description":"olfactory receptor family 2 subfamily AG member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15142]"}, {"versioned_ensembl_gene_id":"ENSG00000279014.1","gene_symbol":"AC051619.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":45214448,"end":45215044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091073.19","gene_symbol":"DTX2","gene_name":"deltex E3 ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:15973]","synonyms":"KIAA1528,RNF58","biotype":"protein_coding","ncbi_id":"113878","summary":"DTX2 functions as an E3 ubiquitin ligase (Takeyama et al., 2003 [PubMed 12670957]).[supplied by OMIM, Nov 2009]","start":76461676,"end":76505995,"strand":1,"description":"deltex E3 ubiquitin ligase 2 [Source:HGNC Symbol;Acc:HGNC:15973]"}, {"versioned_ensembl_gene_id":"ENSG00000275919.1","gene_symbol":"AL161420.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98871742,"end":98872005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102043.15","gene_symbol":"MTMR8","gene_name":"myotubularin related protein 8 [Source:HGNC Symbol;Acc:HGNC:16825]","synonyms":"FLJ20126","biotype":"protein_coding","ncbi_id":"55613","summary":"This gene encodes a member of the myotubularin-related family and is part of the MTMR6 subgroup. Family members are dual-specificity phosphatases and the encoded protein contains a phosphoinositide-binding domain (PID) and a SET-interacting domain (SID). Defects in other family members have been found in myotubular myopathic diseases. [provided by RefSeq, Mar 2010]","start":64268081,"end":64395431,"strand":-1,"description":"myotubularin related protein 8 [Source:HGNC Symbol;Acc:HGNC:16825]"}, {"versioned_ensembl_gene_id":"ENSG00000183549.10","gene_symbol":"ACSM5","gene_name":"acyl-CoA synthetase medium chain family member 5 [Source:HGNC Symbol;Acc:HGNC:26060]","synonyms":"FLJ20581","biotype":"protein_coding","ncbi_id":"54988","summary":null,"start":20409534,"end":20441336,"strand":1,"description":"acyl-CoA synthetase medium chain family member 5 [Source:HGNC Symbol;Acc:HGNC:26060]"}, {"versioned_ensembl_gene_id":"ENSG00000100985.7","gene_symbol":"MMP9","gene_name":"matrix metallopeptidase 9 [Source:HGNC Symbol;Acc:HGNC:7176]","synonyms":"CLG4B","biotype":"protein_coding","ncbi_id":"4318","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The enzyme encoded by this gene degrades type IV and V collagens. Studies in rhesus monkeys suggest that the enzyme is involved in IL-8-induced mobilization of hematopoietic progenitor cells from bone marrow, and murine studies suggest a role in tumor-associated tissue remodeling. [provided by RefSeq, Jul 2008]","start":46008908,"end":46016561,"strand":1,"description":"matrix metallopeptidase 9 [Source:HGNC Symbol;Acc:HGNC:7176]"}, {"versioned_ensembl_gene_id":"ENSG00000114784.3","gene_symbol":"EIF1B","gene_name":"eukaryotic translation initiation factor 1B [Source:HGNC Symbol;Acc:HGNC:30792]","synonyms":"GC20","biotype":"protein_coding","ncbi_id":"10289","summary":null,"start":40309684,"end":40312424,"strand":1,"description":"eukaryotic translation initiation factor 1B [Source:HGNC Symbol;Acc:HGNC:30792]"}, {"versioned_ensembl_gene_id":"ENSG00000232050.1","gene_symbol":"Z98949.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26006389,"end":26006532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233546.1","gene_symbol":"PRYP5","gene_name":"PTPN13-like, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38785]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478933","summary":null,"start":18529358,"end":18529623,"strand":1,"description":"PTPN13-like, Y-linked pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38785]"}, {"versioned_ensembl_gene_id":"ENSG00000231631.6","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"beta5i,LMP7,RING10,D6S216E,PSMB5i","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32931434,"end":32935368,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000133805.15","gene_symbol":"AMPD3","gene_name":"adenosine monophosphate deaminase 3 [Source:HGNC Symbol;Acc:HGNC:470]","synonyms":null,"biotype":"protein_coding","ncbi_id":"272","summary":"This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]","start":10308313,"end":10507579,"strand":1,"description":"adenosine monophosphate deaminase 3 [Source:HGNC Symbol;Acc:HGNC:470]"}, {"versioned_ensembl_gene_id":"ENSG00000164062.12","gene_symbol":"APEH","gene_name":"acylaminoacyl-peptide hydrolase [Source:HGNC Symbol;Acc:HGNC:586]","synonyms":"DNF15S2,D3S48E,D3F15S2","biotype":"protein_coding","ncbi_id":"327","summary":" This gene encodes the enzyme acylpeptide hydrolase, which catalyzes the hydrolysis of the terminal acetylated amino acid preferentially from small acetylated peptides. The acetyl amino acid formed by this hydrolase is further processed to acetate and a free amino acid by an aminoacylase. This gene is located within the same region of chromosome 3 (3p21) as the aminoacylase gene, and deletions at this locus are also associated with a decrease in aminoacylase activity. The acylpeptide hydrolase is a homotetrameric protein of 300 kDa with each subunit consisting of 732 amino acid residues. It can play an important role in destroying oxidatively damaged proteins in living cells. Deletions of this gene locus are found in various types of carcinomas, including small cell lung carcinoma and renal cell carcinoma. [provided by RefSeq, Jul 2008]","start":49674002,"end":49683963,"strand":1,"description":"acylaminoacyl-peptide hydrolase [Source:HGNC Symbol;Acc:HGNC:586]"}, {"versioned_ensembl_gene_id":"ENSG00000166557.12","gene_symbol":"TMED3","gene_name":"transmembrane p24 trafficking protein 3 [Source:HGNC Symbol;Acc:HGNC:28889]","synonyms":"p24gamma4,p24g4,p24B,C15orf22","biotype":"protein_coding","ncbi_id":"23423","summary":null,"start":79311062,"end":79427432,"strand":1,"description":"transmembrane p24 trafficking protein 3 [Source:HGNC Symbol;Acc:HGNC:28889]"}, {"versioned_ensembl_gene_id":"ENSG00000227905.1","gene_symbol":"MED6P1","gene_name":"mediator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128990","summary":null,"start":88048135,"end":88049823,"strand":-1,"description":"mediator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45164]"}, {"versioned_ensembl_gene_id":"ENSG00000273911.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54855924,"end":54864640,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000103591.12","gene_symbol":"AAGAB","gene_name":"alpha and gamma adaptin binding protein [Source:HGNC Symbol;Acc:HGNC:25662]","synonyms":"p34,FLJ11506","biotype":"protein_coding","ncbi_id":"79719","summary":"The protein encoded by this gene interacts with the gamma-adaptin and alpha-adaptin subunits of complexes involved in clathrin-coated vesicle trafficking. Mutations in this gene are associated with type I punctate palmoplantar keratoderma. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]","start":67201033,"end":67255195,"strand":-1,"description":"alpha and gamma adaptin binding protein [Source:HGNC Symbol;Acc:HGNC:25662]"}, {"versioned_ensembl_gene_id":"ENSG00000233015.1","gene_symbol":"SLC25A6P1","gene_name":"solute carrier family 25 member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16554]","synonyms":"SLC25A5L,dJ1065O2.2","biotype":"processed_pseudogene","ncbi_id":"128790","summary":null,"start":21742303,"end":21743077,"strand":-1,"description":"solute carrier family 25 member 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16554]"}, {"versioned_ensembl_gene_id":"ENSG00000239835.1","gene_symbol":"AC092910.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120028740,"end":120029868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154889.16","gene_symbol":"MPPE1","gene_name":"metallophosphoesterase 1 [Source:HGNC Symbol;Acc:HGNC:15988]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65258","summary":null,"start":11882622,"end":11909223,"strand":-1,"description":"metallophosphoesterase 1 [Source:HGNC Symbol;Acc:HGNC:15988]"}, {"versioned_ensembl_gene_id":"ENSG00000168631.12","gene_symbol":"DPCR1","gene_name":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]","synonyms":"bCX105N19.6,PBLT,C6orf37","biotype":"protein_coding","ncbi_id":"135656","summary":null,"start":30934523,"end":30954221,"strand":1,"description":"diffuse panbronchiolitis critical region 1 [Source:HGNC Symbol;Acc:HGNC:21666]"}, {"versioned_ensembl_gene_id":"ENSG00000241158.5","gene_symbol":"ADAMTS9-AS1","gene_name":"ADAMTS9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40625]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929335","summary":null,"start":64561322,"end":64592757,"strand":1,"description":"ADAMTS9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40625]"}, {"versioned_ensembl_gene_id":"ENSG00000267455.1","gene_symbol":"AP005137.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11810406,"end":11811484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274536.6","gene_symbol":"AL034397.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66015461,"end":66020422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213876.4","gene_symbol":"AC120057.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7140930,"end":7141592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177576.11","gene_symbol":"C18orf32","gene_name":"chromosome 18 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:31690]","synonyms":"FLJ23458","biotype":"protein_coding","ncbi_id":"497661","summary":null,"start":49477250,"end":49487252,"strand":-1,"description":"chromosome 18 open reading frame 32 [Source:HGNC Symbol;Acc:HGNC:31690]"}, {"versioned_ensembl_gene_id":"ENSG00000146223.14","gene_symbol":"RPL7L1","gene_name":"ribosomal protein L7 like 1 [Source:HGNC Symbol;Acc:HGNC:21370]","synonyms":"dJ475N16.4","biotype":"protein_coding","ncbi_id":"285855","summary":null,"start":42879618,"end":42889925,"strand":1,"description":"ribosomal protein L7 like 1 [Source:HGNC Symbol;Acc:HGNC:21370]"}, {"versioned_ensembl_gene_id":"ENSG00000282039.1","gene_symbol":"AC246787.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105979291,"end":105979917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278044.1","gene_symbol":"AC023490.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18501794,"end":18512187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282626.1","gene_symbol":"ADAM6","gene_name":"ADAM metallopeptidase domain 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:213]","synonyms":"tMDCIV,C14orf96","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"8755","summary":null,"start":105970500,"end":105973040,"strand":-1,"description":"ADAM metallopeptidase domain 6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:213]"}, {"versioned_ensembl_gene_id":"ENSG00000150961.14","gene_symbol":"SEC24D","gene_name":"SEC24 homolog D, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10706]","synonyms":"KIAA0755","biotype":"protein_coding","ncbi_id":"9871","summary":"The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. This gene product is implicated in the shaping of the vesicle, and also in cargo selection and concentration. Mutations in this gene have been associated with Cole-Carpenter syndrome, a disorder affecting bone formation, resulting in craniofacial malformations and bones that break easily. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":118722823,"end":118838683,"strand":-1,"description":"SEC24 homolog D, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:10706]"}, {"versioned_ensembl_gene_id":"ENSG00000216710.1","gene_symbol":"COX6A1P3","gene_name":"cytochrome c oxidase subunit 6A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37633]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287768","summary":null,"start":120781220,"end":120781512,"strand":1,"description":"cytochrome c oxidase subunit 6A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37633]"}, {"versioned_ensembl_gene_id":"ENSG00000281929.1","gene_symbol":"AC243757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16179193,"end":16180211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249089.1","gene_symbol":"AIG1P1","gene_name":"androgen induced 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43926]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479028","summary":null,"start":39022411,"end":39022558,"strand":1,"description":"androgen induced 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43926]"}, {"versioned_ensembl_gene_id":"ENSG00000226010.1","gene_symbol":"AL355852.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64144872,"end":64147052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250561.2","gene_symbol":"AC079804.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6879627,"end":6880626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100079.6","gene_symbol":"LGALS2","gene_name":"galectin 2 [Source:HGNC Symbol;Acc:HGNC:6562]","synonyms":"HL14","biotype":"protein_coding","ncbi_id":"3957","summary":"The protein encoded by this gene is a soluble beta-galactoside binding lectin. The encoded protein is found as a homodimer and can bind to lymphotoxin-alpha. A single nucleotide polymorphism in an intron of this gene can alter the transcriptional level of the protein, with a resultant increased risk of myocardial infarction. [provided by RefSeq, Jul 2008]","start":37570246,"end":37582616,"strand":-1,"description":"galectin 2 [Source:HGNC Symbol;Acc:HGNC:6562]"}, {"versioned_ensembl_gene_id":"ENSG00000234378.1","gene_symbol":"AC098828.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20063856,"end":20106829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235071.1","gene_symbol":"AC073909.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16474342,"end":16475340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206199.10","gene_symbol":"ANKUB1","gene_name":"ankyrin repeat and ubiquitin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29642]","synonyms":"C3orf16","biotype":"protein_coding","ncbi_id":"389161","summary":null,"start":149761100,"end":149968385,"strand":-1,"description":"ankyrin repeat and ubiquitin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29642]"}, {"versioned_ensembl_gene_id":"ENSG00000283228.1","gene_symbol":"AC068547.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":151802651,"end":151973949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242791.2","gene_symbol":"AC117395.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149976755,"end":149979355,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261336.1","gene_symbol":"EIF4BP5","gene_name":"eukaryotic translation initiation factor 4B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37938]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421528","summary":null,"start":47565090,"end":47566884,"strand":-1,"description":"eukaryotic translation initiation factor 4B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37938]"}, {"versioned_ensembl_gene_id":"ENSG00000203335.4","gene_symbol":"AC006019.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154055585,"end":154059561,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181804.14","gene_symbol":"SLC9A9","gene_name":"solute carrier family 9 member A9 [Source:HGNC Symbol;Acc:HGNC:20653]","synonyms":"NHE9,FLJ35613","biotype":"protein_coding","ncbi_id":"285195","summary":"This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]","start":143265222,"end":143848531,"strand":-1,"description":"solute carrier family 9 member A9 [Source:HGNC Symbol;Acc:HGNC:20653]"}, {"versioned_ensembl_gene_id":"ENSG00000244493.1","gene_symbol":"SLC9A9-AS2","gene_name":"SLC9A9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40929]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106480356","summary":null,"start":143381338,"end":143382161,"strand":1,"description":"SLC9A9 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40929]"}, {"versioned_ensembl_gene_id":"ENSG00000231677.1","gene_symbol":"HLA-DQB1-AS1","gene_name":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480429","summary":null,"start":32582940,"end":32583789,"strand":1,"description":"HLA-DQB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39762]"}, {"versioned_ensembl_gene_id":"ENSG00000213699.8","gene_symbol":"SLC35F6","gene_name":"solute carrier family 35 member F6 [Source:HGNC Symbol;Acc:HGNC:26055]","synonyms":"TANGO9,FLJ20555,C2orf18,ANT2BP","biotype":"protein_coding","ncbi_id":"54978","summary":null,"start":26764284,"end":26781231,"strand":1,"description":"solute carrier family 35 member F6 [Source:HGNC Symbol;Acc:HGNC:26055]"}, {"versioned_ensembl_gene_id":"ENSG00000260759.1","gene_symbol":"AP001120.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11666456,"end":11670165,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235094.2","gene_symbol":"AC006335.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6306042,"end":6307920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143947.13","gene_symbol":"RPS27A","gene_name":"ribosomal protein S27a [Source:HGNC Symbol;Acc:HGNC:10417]","synonyms":"UBCEP80,Uba80,S27A","biotype":"protein_coding","ncbi_id":"6233","summary":"Ubiquitin, a highly conserved protein that has a major role in targeting cellular proteins for degradation by the 26S proteosome, is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin fused to an unrelated protein. This gene encodes a fusion protein consisting of ubiquitin at the N terminus and ribosomal protein S27a at the C terminus. When expressed in yeast, the protein is post-translationally processed, generating free ubiquitin monomer and ribosomal protein S27a. Ribosomal protein S27a is a component of the 40S subunit of the ribosome and belongs to the S27AE family of ribosomal proteins. It contains C4-type zinc finger domains and is located in the cytoplasm. Pseudogenes derived from this gene are present in the genome. As with ribosomal protein S27a, ribosomal protein L40 is also synthesized as a fusion protein with ubiquitin; similarly, ribosomal protein S30 is synthesized as a fusion protein with the ubiquitin-like protein fubi. Multiple alternatively spliced transcript variants that encode the same proteins have been identified.[provided by RefSeq, Sep 2008]","start":55231903,"end":55235853,"strand":1,"description":"ribosomal protein S27a [Source:HGNC Symbol;Acc:HGNC:10417]"}, {"versioned_ensembl_gene_id":"ENSG00000132854.18","gene_symbol":"KANK4","gene_name":"KN motif and ankyrin repeat domains 4 [Source:HGNC Symbol;Acc:HGNC:27263]","synonyms":"KIAA0172,ANKRD38","biotype":"protein_coding","ncbi_id":"163782","summary":null,"start":62236979,"end":62319414,"strand":-1,"description":"KN motif and ankyrin repeat domains 4 [Source:HGNC Symbol;Acc:HGNC:27263]"}, {"versioned_ensembl_gene_id":"ENSG00000235609.7","gene_symbol":"AF127577.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14818843,"end":15014430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101489.19","gene_symbol":"CELF4","gene_name":"CUGBP Elav-like family member 4 [Source:HGNC Symbol;Acc:HGNC:14015]","synonyms":"BRUNOL4","biotype":"protein_coding","ncbi_id":"56853","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":37243047,"end":37566037,"strand":-1,"description":"CUGBP Elav-like family member 4 [Source:HGNC Symbol;Acc:HGNC:14015]"}, {"versioned_ensembl_gene_id":"ENSG00000231618.10","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32229863,"end":32248406,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000259581.3","gene_symbol":"TYRO3P","gene_name":"TYRO3P protein tyrosine kinase pseudogene [Source:HGNC Symbol;Acc:HGNC:12447]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"7302","summary":null,"start":76258986,"end":76261690,"strand":-1,"description":"TYRO3P protein tyrosine kinase pseudogene [Source:HGNC Symbol;Acc:HGNC:12447]"}, {"versioned_ensembl_gene_id":"ENSG00000177689.10","gene_symbol":"MAGEB10","gene_name":"MAGE family member B10 [Source:HGNC Symbol;Acc:HGNC:25377]","synonyms":"FLJ32965","biotype":"protein_coding","ncbi_id":"139422","summary":"This gene encodes a member of the B subfamily of the melanoma associated antigen protein family. The encoded protein is specifically expressed in testis and tumor cells. [provided by RefSeq, Apr 2010]","start":27807990,"end":27823014,"strand":1,"description":"MAGE family member B10 [Source:HGNC Symbol;Acc:HGNC:25377]"}, {"versioned_ensembl_gene_id":"ENSG00000243073.3","gene_symbol":"PRAMEF4","gene_name":"PRAME family member 4 [Source:HGNC Symbol;Acc:HGNC:31971]","synonyms":"RP5-845O24.6","biotype":"protein_coding","ncbi_id":"400735","summary":null,"start":12879224,"end":12886201,"strand":-1,"description":"PRAME family member 4 [Source:HGNC Symbol;Acc:HGNC:31971]"}, {"versioned_ensembl_gene_id":"ENSG00000125912.10","gene_symbol":"NCLN","gene_name":"nicalin [Source:HGNC Symbol;Acc:HGNC:26923]","synonyms":"NICALIN,NET59","biotype":"protein_coding","ncbi_id":"56926","summary":null,"start":3185563,"end":3209575,"strand":1,"description":"nicalin [Source:HGNC Symbol;Acc:HGNC:26923]"}, {"versioned_ensembl_gene_id":"ENSG00000158578.18","gene_symbol":"ALAS2","gene_name":"5'-aminolevulinate synthase 2 [Source:HGNC Symbol;Acc:HGNC:397]","synonyms":"ASB","biotype":"protein_coding","ncbi_id":"212","summary":"The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pathway. Defects in this gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":55009055,"end":55031064,"strand":-1,"description":"5'-aminolevulinate synthase 2 [Source:HGNC Symbol;Acc:HGNC:397]"}, {"versioned_ensembl_gene_id":"ENSG00000267773.1","gene_symbol":"AP001120.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11644336,"end":11644824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249628.2","gene_symbol":"LINC00942","gene_name":"long intergenic non-protein coding RNA 942 [Source:HGNC Symbol;Acc:HGNC:48636]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100292680","summary":null,"start":1500525,"end":1507318,"strand":-1,"description":"long intergenic non-protein coding RNA 942 [Source:HGNC Symbol;Acc:HGNC:48636]"}, {"versioned_ensembl_gene_id":"ENSG00000159140.19","gene_symbol":"SON","gene_name":"SON DNA binding protein [Source:HGNC Symbol;Acc:HGNC:11183]","synonyms":"FLJ21099,DBP-5,C21orf50,BASS1,NREBP,KIAA1019,FLJ33914","biotype":"protein_coding","ncbi_id":"6651","summary":"This gene encodes a protein that contains multiple simple repeats. The encoded protein binds RNA and promotes pre-mRNA splicing, particularly of transcripts with poor splice sites. The protein also recognizes a specific DNA sequence found in the human hepatitis B virus (HBV) and represses HBV core promoter activity. There is a pseudogene for this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":33542618,"end":33577481,"strand":1,"description":"SON DNA binding protein [Source:HGNC Symbol;Acc:HGNC:11183]"}, {"versioned_ensembl_gene_id":"ENSG00000273844.1","gene_symbol":"AL139418.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":196970495,"end":196970671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225295.1","gene_symbol":"MTND4P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42191]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873190","summary":null,"start":57169406,"end":57170771,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42191]"}, {"versioned_ensembl_gene_id":"ENSG00000283230.1","gene_symbol":"AC099654.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57168725,"end":57169074,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267143.1","gene_symbol":"AP001120.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11620717,"end":11621158,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071909.18","gene_symbol":"MYO3B","gene_name":"myosin IIIB [Source:HGNC Symbol;Acc:HGNC:15576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140469","summary":"This gene encodes one of the class III myosins. Myosins are ATPases, activated by actin, that move along actin filaments in the cell. This class of myosins are characterized by an amino-terminal kinase domain and shown to be present in photoreceptors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":170178145,"end":170655171,"strand":1,"description":"myosin IIIB [Source:HGNC Symbol;Acc:HGNC:15576]"}, {"versioned_ensembl_gene_id":"ENSG00000007062.11","gene_symbol":"PROM1","gene_name":"prominin 1 [Source:HGNC Symbol;Acc:HGNC:9454]","synonyms":"STGD4,RP41,PROML1,MCDR2,CORD12,CD133,AC133","biotype":"protein_coding","ncbi_id":"8842","summary":"This gene encodes a pentaspan transmembrane glycoprotein. The protein localizes to membrane protrusions and is often expressed on adult stem cells, where it is thought to function in maintaining stem cell properties by suppressing differentiation. Mutations in this gene have been shown to result in retinitis pigmentosa and Stargardt disease. Expression of this gene is also associated with several types of cancer. This gene is expressed from at least five alternative promoters that are expressed in a tissue-dependent manner. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":15963076,"end":16084378,"strand":-1,"description":"prominin 1 [Source:HGNC Symbol;Acc:HGNC:9454]"}, {"versioned_ensembl_gene_id":"ENSG00000266909.1","gene_symbol":"SLC25A6P4","gene_name":"solute carrier family 25 member 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43853]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422690","summary":null,"start":80077707,"end":80078259,"strand":1,"description":"solute carrier family 25 member 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43853]"}, {"versioned_ensembl_gene_id":"ENSG00000231898.8","gene_symbol":"AC012594.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":170332085,"end":170408564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244065.1","gene_symbol":"MARK2P17","gene_name":"microtubule affinity regulating kinase 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:50318]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421499","summary":null,"start":128843564,"end":128844404,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:50318]"}, {"versioned_ensembl_gene_id":"ENSG00000181830.8","gene_symbol":"SLC35C1","gene_name":"solute carrier family 35 member C1 [Source:HGNC Symbol;Acc:HGNC:20197]","synonyms":"FUCT1,FLJ11320","biotype":"protein_coding","ncbi_id":"55343","summary":"This gene encodes a GDP-fucose transporter that is found in the Golgi apparatus. Mutations in this gene result in congenital disorder of glycosylation type IIc. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]","start":45804072,"end":45813015,"strand":1,"description":"solute carrier family 35 member C1 [Source:HGNC Symbol;Acc:HGNC:20197]"}, {"versioned_ensembl_gene_id":"ENSG00000226413.2","gene_symbol":"OR8T1P","gene_name":"olfactory receptor family 8 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:19630]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"282791","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48442030,"end":48442947,"strand":-1,"description":"olfactory receptor family 8 subfamily T member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:19630]"}, {"versioned_ensembl_gene_id":"ENSG00000283945.1","gene_symbol":"LINC00032","gene_name":"long intergenic non-protein coding RNA 32 [Source:HGNC Symbol;Acc:HGNC:16506]","synonyms":"NCRNA00032,C9orf14","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"158035","summary":null,"start":27245680,"end":27284869,"strand":-1,"description":"long intergenic non-protein coding RNA 32 [Source:HGNC Symbol;Acc:HGNC:16506]"}, {"versioned_ensembl_gene_id":"ENSG00000173557.14","gene_symbol":"C2orf70","gene_name":"chromosome 2 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:27938]","synonyms":"LOC339778","biotype":"protein_coding","ncbi_id":"339778","summary":null,"start":26562582,"end":26579532,"strand":1,"description":"chromosome 2 open reading frame 70 [Source:HGNC Symbol;Acc:HGNC:27938]"}, {"versioned_ensembl_gene_id":"ENSG00000258197.1","gene_symbol":"NKX2-2-AS1","gene_name":"NKX2-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37154]","synonyms":"NKX2-2AS","biotype":"antisense_RNA","ncbi_id":"100874189","summary":null,"start":21511447,"end":21512309,"strand":1,"description":"NKX2-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37154]"}, {"versioned_ensembl_gene_id":"ENSG00000227634.2","gene_symbol":"LINC01714","gene_name":"long intergenic non-protein coding RNA 1714 [Source:HGNC Symbol;Acc:HGNC:52501]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724539","summary":null,"start":8202429,"end":8215210,"strand":1,"description":"long intergenic non-protein coding RNA 1714 [Source:HGNC Symbol;Acc:HGNC:52501]"}, {"versioned_ensembl_gene_id":"ENSG00000276914.2","gene_symbol":"FOPNL","gene_name":"FGFR1OP N-terminal like [Source:HGNC Symbol;Acc:HGNC:26435]","synonyms":"PHSECRG2,FOR20,FLJ31153,DKFZp686N1651,C16orf63","biotype":"protein_coding","ncbi_id":"123811","summary":null,"start":15950862,"end":15973769,"strand":-1,"description":"FGFR1OP N-terminal like [Source:HGNC Symbol;Acc:HGNC:26435]"}, {"versioned_ensembl_gene_id":"ENSG00000257666.1","gene_symbol":"CBX3P5","gene_name":"chromobox 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42877]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421943","summary":null,"start":95286318,"end":95286838,"strand":-1,"description":"chromobox 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42877]"}, {"versioned_ensembl_gene_id":"ENSG00000163832.15","gene_symbol":"ELP6","gene_name":"elongator acetyltransferase complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25976]","synonyms":"C3orf75,TMEM103,FLJ20211","biotype":"protein_coding","ncbi_id":"54859","summary":null,"start":47495640,"end":47513761,"strand":-1,"description":"elongator acetyltransferase complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25976]"}, {"versioned_ensembl_gene_id":"ENSG00000259866.1","gene_symbol":"AC007599.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47561307,"end":47562480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225795.1","gene_symbol":"AC006463.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122676580,"end":122676811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260744.1","gene_symbol":"AC007494.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47196311,"end":47202429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158290.16","gene_symbol":"CUL4B","gene_name":"cullin 4B [Source:HGNC Symbol;Acc:HGNC:2555]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8450","summary":"This gene is a member of the cullin family. The encoded protein forms a complex that functions as an E3 ubiquitin ligase and catalyzes the polyubiquitination of specific protein substrates in the cell. The protein interacts with a ring finger protein, and is required for the proteolysis of several regulators of DNA replication including chromatin licensing and DNA replication factor 1 and cyclin E. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":120524609,"end":120575794,"strand":-1,"description":"cullin 4B [Source:HGNC Symbol;Acc:HGNC:2555]"}, {"versioned_ensembl_gene_id":"ENSG00000240563.1","gene_symbol":"L1TD1","gene_name":"LINE1 type transposase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25595]","synonyms":"FLJ10884,ECAT11","biotype":"protein_coding","ncbi_id":"54596","summary":null,"start":62194831,"end":62212328,"strand":1,"description":"LINE1 type transposase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25595]"}, {"versioned_ensembl_gene_id":"ENSG00000140455.16","gene_symbol":"USP3","gene_name":"ubiquitin specific peptidase 3 [Source:HGNC Symbol;Acc:HGNC:12626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9960","summary":null,"start":63504511,"end":63594640,"strand":1,"description":"ubiquitin specific peptidase 3 [Source:HGNC Symbol;Acc:HGNC:12626]"}, {"versioned_ensembl_gene_id":"ENSG00000284705.1","gene_symbol":"AL596257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36703953,"end":36710582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284720.1","gene_symbol":"AC117945.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36768122,"end":36769725,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215035.2","gene_symbol":"FDPSP5","gene_name":"farnesyl diphosphate synthase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3636]","synonyms":"FDPSL5,CHR39C,FPSL5","biotype":"processed_pseudogene","ncbi_id":"2229","summary":null,"start":44476027,"end":44477422,"strand":-1,"description":"farnesyl diphosphate synthase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:3636]"}, {"versioned_ensembl_gene_id":"ENSG00000227526.4","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206,HLA-DR1BL,D6S206E,HLA-DRB1L","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32408020,"end":32421718,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000261115.5","gene_symbol":"TMEM178B","gene_name":"transmembrane protein 178B [Source:HGNC Symbol;Acc:HGNC:44112]","synonyms":"DKFZp547G036","biotype":"protein_coding","ncbi_id":"100507421","summary":null,"start":141074232,"end":141480380,"strand":1,"description":"transmembrane protein 178B [Source:HGNC Symbol;Acc:HGNC:44112]"}, {"versioned_ensembl_gene_id":"ENSG00000255041.1","gene_symbol":"AC103855.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45387215,"end":45513802,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007392.16","gene_symbol":"LUC7L","gene_name":"LUC7 like [Source:HGNC Symbol;Acc:HGNC:6723]","synonyms":"LUC7B1,Luc7,hLuc7B1","biotype":"protein_coding","ncbi_id":"55692","summary":"The LUC7L gene may represent a mammalian heterochromatic gene, encoding a putative RNA-binding protein similar to the yeast Luc7p subunit of the U1 snRNP splicing complex that is normally required for 5-prime splice site selection (Tufarelli et al., 2001 [PubMed 11170747]).[supplied by OMIM, Mar 2008]","start":188969,"end":229463,"strand":-1,"description":"LUC7 like [Source:HGNC Symbol;Acc:HGNC:6723]"}, {"versioned_ensembl_gene_id":"ENSG00000251687.1","gene_symbol":"AC104791.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145833118,"end":145839580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100353.17","gene_symbol":"EIF3D","gene_name":"eukaryotic translation initiation factor 3 subunit D [Source:HGNC Symbol;Acc:HGNC:3278]","synonyms":"EIF3S7,eIF3d,eIF3-zeta,eIF3-p66","biotype":"protein_coding","ncbi_id":"8664","summary":"Eukaryotic translation initiation factor-3 (eIF3), the largest of the eIFs, is a multiprotein complex composed of at least ten nonidentical subunits. The complex binds to the 40S ribosome and helps maintain the 40S and 60S ribosomal subunits in a dissociated state. It is also thought to play a role in the formation of the 40S initiation complex by interacting with the ternary complex of eIF2/GTP/methionyl-tRNA, and by promoting mRNA binding. The protein encoded by this gene is the major RNA binding subunit of the eIF3 complex. [provided by RefSeq, Jul 2008]","start":36510850,"end":36529436,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit D [Source:HGNC Symbol;Acc:HGNC:3278]"}, {"versioned_ensembl_gene_id":"ENSG00000250475.1","gene_symbol":"AC017037.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":157968412,"end":157969615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276196.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54732699,"end":54744341,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000100836.10","gene_symbol":"PABPN1","gene_name":"poly(A) binding protein nuclear 1 [Source:HGNC Symbol;Acc:HGNC:8565]","synonyms":"PABP2,PAB2,OPMD","biotype":"protein_coding","ncbi_id":"8106","summary":"This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails at the 3' ends of eukaryotic transcripts and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. This gene contains a GCG trinucleotide repeat at the 5' end of the coding region, and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene. [provided by RefSeq, Dec 2010]","start":23321289,"end":23326185,"strand":1,"description":"poly(A) binding protein nuclear 1 [Source:HGNC Symbol;Acc:HGNC:8565]"}, {"versioned_ensembl_gene_id":"ENSG00000101361.16","gene_symbol":"NOP56","gene_name":"NOP56 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:15911]","synonyms":"SCA36,NOL5A","biotype":"protein_coding","ncbi_id":"10528","summary":"Nop56p is a yeast nucleolar protein that is part of a complex with the nucleolar proteins Nop58p and fibrillarin. Nop56p is required for assembly of the 60S ribosomal subunit and is involved in pre-rRNA processing. The protein encoded by this gene is similar in sequence to Nop56p and is also found in the nucleolus. Expansion of a GGCCTG repeat from 3-8 copies to 1500-2500 copies in an intron of this gene results in spinocerebellar ataxia 36. Multiple transcript variants encoding several different isoforms have been found for this gene, but the full-length nature of most of them has not been determined. [provided by RefSeq, Jul 2016]","start":2652145,"end":2658393,"strand":1,"description":"NOP56 ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:15911]"}, {"versioned_ensembl_gene_id":"ENSG00000090263.15","gene_symbol":"MRPS33","gene_name":"mitochondrial ribosomal protein S33 [Source:HGNC Symbol;Acc:HGNC:16634]","synonyms":"CGI-139","biotype":"protein_coding","ncbi_id":"51650","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. The 28S subunit of the mammalian mitoribosome may play a crucial and characteristic role in translation initiation. This gene encodes a 28S subunit protein that is one of the more highly conserved mitochondrial ribosomal proteins among mammals, Drosophila and C. elegans. Splice variants that differ in the 5' UTR have been found for this gene; all variants encode the same protein. Pseudogenes corresponding to this gene are found on chromosomes 1q, 4p, 4q, and 20q [provided by RefSeq, Jul 2008]","start":141002610,"end":141015228,"strand":-1,"description":"mitochondrial ribosomal protein S33 [Source:HGNC Symbol;Acc:HGNC:16634]"}, {"versioned_ensembl_gene_id":"ENSG00000198680.4","gene_symbol":"TUSC1","gene_name":"tumor suppressor candidate 1 [Source:HGNC Symbol;Acc:HGNC:31010]","synonyms":"TSG-9,CCDC89B","biotype":"protein_coding","ncbi_id":"286319","summary":"This gene is located within the region of chromosome 9p that harbors tumor suppressor genes critical in carcinogenesis. It is an intronless gene which is downregulated in non-small-cell lung cancer and small-cell lung cancer cell lines, suggesting that it may play a role in lung tumorigenesis. [provided by RefSeq, Jul 2008]","start":25676389,"end":25678440,"strand":-1,"description":"tumor suppressor candidate 1 [Source:HGNC Symbol;Acc:HGNC:31010]"}, {"versioned_ensembl_gene_id":"ENSG00000122042.9","gene_symbol":"UBL3","gene_name":"ubiquitin like 3 [Source:HGNC Symbol;Acc:HGNC:12504]","synonyms":"PNSC1,HCG-1,FLJ32018,DKFZP434K151","biotype":"protein_coding","ncbi_id":"5412","summary":null,"start":29764371,"end":29850684,"strand":-1,"description":"ubiquitin like 3 [Source:HGNC Symbol;Acc:HGNC:12504]"}, {"versioned_ensembl_gene_id":"ENSG00000130768.14","gene_symbol":"SMPDL3B","gene_name":"sphingomyelin phosphodiesterase acid like 3B [Source:HGNC Symbol;Acc:HGNC:21416]","synonyms":"ASML3B","biotype":"protein_coding","ncbi_id":"27293","summary":null,"start":27934993,"end":27959157,"strand":1,"description":"sphingomyelin phosphodiesterase acid like 3B [Source:HGNC Symbol;Acc:HGNC:21416]"}, {"versioned_ensembl_gene_id":"ENSG00000123219.12","gene_symbol":"CENPK","gene_name":"centromere protein K [Source:HGNC Symbol;Acc:HGNC:29479]","synonyms":"SOLT,FKSG14,CENP-K","biotype":"protein_coding","ncbi_id":"64105","summary":"CENPK is a subunit of a CENPH (MIM 605607)-CENPI (MIM 300065)-associated centromeric complex that targets CENPA (MIM 117139) to centromeres and is required for proper kinetochore function and mitotic progression (Okada et al., 2006 [PubMed 16622420]).[supplied by OMIM, Mar 2008]","start":65517766,"end":65563171,"strand":-1,"description":"centromere protein K [Source:HGNC Symbol;Acc:HGNC:29479]"}, {"versioned_ensembl_gene_id":"ENSG00000168828.5","gene_symbol":"OR13J1","gene_name":"olfactory receptor family 13 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:15108]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392309","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":35869263,"end":35870601,"strand":-1,"description":"olfactory receptor family 13 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:15108]"}, {"versioned_ensembl_gene_id":"ENSG00000251478.1","gene_symbol":"AC008817.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41585882,"end":41587787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000094661.3","gene_symbol":"OR1I1","gene_name":"olfactory receptor family 1 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:8207]","synonyms":"OR1I1Q,OR1I1P,OR19-20","biotype":"protein_coding","ncbi_id":"126370","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":15082211,"end":15092970,"strand":1,"description":"olfactory receptor family 1 subfamily I member 1 [Source:HGNC Symbol;Acc:HGNC:8207]"}, {"versioned_ensembl_gene_id":"ENSG00000198018.6","gene_symbol":"ENTPD7","gene_name":"ectonucleoside triphosphate diphosphohydrolase 7 [Source:HGNC Symbol;Acc:HGNC:19745]","synonyms":"LALP1,FLJ30978","biotype":"protein_coding","ncbi_id":"57089","summary":"This gene encodes a purine-converting ectoenzyme which belongs to the ecto-nucleoside triphosphate diphosphohydrolase (E-NTPDase) family. The encoded protein hydrolyzes extracellular nucleoside triphosphates (UTP, GTP, and CTP) to nucleoside monophosphates as part of a purinergic signaling pathway. It contains two transmembrane domains at the N- and C-termini and a large, hydrophobic catalytic domain located in between. This gene affects oxidative stress as well as DNA damage and is a mediator of senescence. [provided by RefSeq, Mar 2017]","start":99659506,"end":99706240,"strand":1,"description":"ectonucleoside triphosphate diphosphohydrolase 7 [Source:HGNC Symbol;Acc:HGNC:19745]"}, {"versioned_ensembl_gene_id":"ENSG00000166971.16","gene_symbol":"AKTIP","gene_name":"AKT interacting protein [Source:HGNC Symbol;Acc:HGNC:16710]","synonyms":"FTS,FLJ13258","biotype":"protein_coding","ncbi_id":"64400","summary":"The mouse homolog of this gene produces fused toes and thymic hyperplasia in heterozygous mutant animals while homozygous mutants die in early development. This gene may play a role in apoptosis as these morphological abnormalities are caused by altered patterns of programmed cell death. The protein encoded by this gene is similar to the ubiquitin ligase domain of other ubiquitin-conjugating enzymes but lacks the conserved cysteine residue that enables those enzymes to conjugate ubiquitin to the target protein. This protein interacts directly with serine/threonine kinase protein kinase B (PKB)/Akt and modulates PKB activity by enhancing the phosphorylation of PKB's regulatory sites. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":53491040,"end":53504411,"strand":-1,"description":"AKT interacting protein [Source:HGNC Symbol;Acc:HGNC:16710]"}, {"versioned_ensembl_gene_id":"ENSG00000259573.1","gene_symbol":"NMNAT1P5","gene_name":"NMNAT1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49167]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129256","summary":null,"start":59964942,"end":59966084,"strand":1,"description":"NMNAT1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49167]"}, {"versioned_ensembl_gene_id":"ENSG00000279722.1","gene_symbol":"AC007342.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53487607,"end":53489943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262666.5","gene_symbol":"FAM189B","gene_name":"family with sequence similarity 189 member B [Source:HGNC Symbol;Acc:HGNC:1233]","synonyms":"cote1,C1orf2","biotype":"protein_coding","ncbi_id":"10712","summary":"This gene is located near the gene for the lysosomal enzyme glucosylceramidase; a deficiency in this enzyme is associated with Gaucher disease. The encoded protein has been identified as a potential binding partner of a WW domain-containing protein which is involved in apoptosis and tumor suppression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":155262609,"end":155270887,"strand":-1,"description":"family with sequence similarity 189 member B [Source:HGNC Symbol;Acc:HGNC:1233]"}, {"versioned_ensembl_gene_id":"ENSG00000258835.1","gene_symbol":"TRAV28","gene_name":"T-cell receptor alpha variable 28 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12126]","synonyms":null,"biotype":"TR_V_pseudogene","ncbi_id":"28654","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22155079,"end":22155638,"strand":1,"description":"T-cell receptor alpha variable 28 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12126]"}, {"versioned_ensembl_gene_id":"ENSG00000085276.17","gene_symbol":"MECOM","gene_name":"MDS1 and EVI1 complex locus [Source:HGNC Symbol;Acc:HGNC:3498]","synonyms":"PRDM3,MDS1-EVI1,MDS1,KMT8E,EVI1","biotype":"protein_coding","ncbi_id":"2122","summary":"The protein encoded by this gene is a transcriptional regulator and oncoprotein that may be involved in hematopoiesis, apoptosis, development, and cell differentiation and proliferation. The encoded protein can interact with CTBP1, SMAD3, CREBBP, KAT2B, MAPK8, and MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene and the onset of leukemia. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":169083499,"end":169663618,"strand":-1,"description":"MDS1 and EVI1 complex locus [Source:HGNC Symbol;Acc:HGNC:3498]"}, {"versioned_ensembl_gene_id":"ENSG00000228107.1","gene_symbol":"AP000692.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":36360630,"end":36362040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236890.2","gene_symbol":"AC016027.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18081466,"end":18081675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104131.12","gene_symbol":"EIF3J","gene_name":"eukaryotic translation initiation factor 3 subunit J [Source:HGNC Symbol;Acc:HGNC:3270]","synonyms":"eIF3-alpha,EIF3S1,eIF3j,eIF3-p35","biotype":"protein_coding","ncbi_id":"8669","summary":"This gene encodes a core subunit of the eukaryotic initiation factor 3 complex, which participates in the initiation of translation by aiding in the recruitment of protein and mRNA components to the 40S ribosome. There are pseudogenes for this gene on chromosomes 1, 3, and 9. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013]","start":44537057,"end":44563029,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit J [Source:HGNC Symbol;Acc:HGNC:3270]"}, {"versioned_ensembl_gene_id":"ENSG00000211809.2","gene_symbol":"TRAV27","gene_name":"T-cell receptor alpha variable 27 [Source:HGNC Symbol;Acc:HGNC:12125]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28655","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":22147995,"end":22148633,"strand":1,"description":"T-cell receptor alpha variable 27 [Source:HGNC Symbol;Acc:HGNC:12125]"}, {"versioned_ensembl_gene_id":"ENSG00000117519.15","gene_symbol":"CNN3","gene_name":"calponin 3 [Source:HGNC Symbol;Acc:HGNC:2157]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1266","summary":"This gene encodes a protein with a markedly acidic C terminus; the basic N-terminus is highly homologous to the N-terminus of a related gene, CNN1. Members of the CNN gene family all contain similar tandemly repeated motifs. This encoded protein is associated with the cytoskeleton but is not involved in contraction. [provided by RefSeq, Jul 2008]","start":94896949,"end":94927278,"strand":-1,"description":"calponin 3 [Source:HGNC Symbol;Acc:HGNC:2157]"}, {"versioned_ensembl_gene_id":"ENSG00000211796.1","gene_symbol":"TRAV16","gene_name":"T-cell receptor alpha variable 16 [Source:HGNC Symbol;Acc:HGNC:12112]","synonyms":"TCRAV9S1,TCRAV16S1","biotype":"TR_V_gene","ncbi_id":"28667","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21990496,"end":21990938,"strand":1,"description":"T-cell receptor alpha variable 16 [Source:HGNC Symbol;Acc:HGNC:12112]"}, {"versioned_ensembl_gene_id":"ENSG00000159259.7","gene_symbol":"CHAF1B","gene_name":"chromatin assembly factor 1 subunit B [Source:HGNC Symbol;Acc:HGNC:1911]","synonyms":"MPP7,MPHOSPH7,CAF1P60,CAF1A,CAF1,CAF-1","biotype":"protein_coding","ncbi_id":"8208","summary":"Chromatin assembly factor I (CAF-I) is required for the assembly of histone octamers onto newly-replicated DNA. CAF-I is composed of three protein subunits, p50, p60, and p150. The protein encoded by this gene corresponds to the p60 subunit and is required for chromatin assembly after replication. The encoded protein is differentially phosphorylated in a cell cycle-dependent manner. In addition, it is normally found in the nucleus except during mitosis, when it is released into the cytoplasm. This protein is a member of the WD-repeat HIR1 family and may also be involved in DNA repair. [provided by RefSeq, Jul 2008]","start":36385378,"end":36419015,"strand":1,"description":"chromatin assembly factor 1 subunit B [Source:HGNC Symbol;Acc:HGNC:1911]"}, {"versioned_ensembl_gene_id":"ENSG00000258557.1","gene_symbol":"AC245505.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21962819,"end":21963042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257376.1","gene_symbol":"AC079601.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42431665,"end":42433357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258482.1","gene_symbol":"TRAV15","gene_name":"T-cell receptor alpha variable 15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12111]","synonyms":"TCRAV15S1","biotype":"TR_V_pseudogene","ncbi_id":"28668","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21950406,"end":21950654,"strand":1,"description":"T-cell receptor alpha variable 15 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12111]"}, {"versioned_ensembl_gene_id":"ENSG00000235464.1","gene_symbol":"AC007652.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35496021,"end":35510263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000053524.12","gene_symbol":"MCF2L2","gene_name":"MCF.2 cell line derived transforming sequence-like 2 [Source:HGNC Symbol;Acc:HGNC:30319]","synonyms":"KIAA0861,ARHGEF22","biotype":"protein_coding","ncbi_id":"23101","summary":null,"start":183178043,"end":183428778,"strand":-1,"description":"MCF.2 cell line derived transforming sequence-like 2 [Source:HGNC Symbol;Acc:HGNC:30319]"}, {"versioned_ensembl_gene_id":"ENSG00000272798.1","gene_symbol":"AL008721.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25436312,"end":25436915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271138.1","gene_symbol":"IGLVIVOR22-1","gene_name":"immunoglobulin lambda variable (IV)/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15694]","synonyms":"IGLV(IV)/OR22-1","biotype":"IG_V_pseudogene","ncbi_id":"84088","summary":null,"start":25437306,"end":25437823,"strand":-1,"description":"immunoglobulin lambda variable (IV)/OR22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15694]"}, {"versioned_ensembl_gene_id":"ENSG00000176597.11","gene_symbol":"B3GNT5","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:15684]","synonyms":"beta3Gn-T5,B3GN-T5","biotype":"protein_coding","ncbi_id":"84002","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase family. This enzyme is a type II membrane protein. It exhibits strong activity to transfer GlcNAc to glycolipid substrates and is identified as the most likely candidate for lactotriaosylceramide synthase. This enzyme is essential for the expression of Lewis X epitopes on glycolipids. [provided by RefSeq, Jul 2008]","start":183253244,"end":183298504,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:15684]"}, {"versioned_ensembl_gene_id":"ENSG00000135317.12","gene_symbol":"SNX14","gene_name":"sorting nexin 14 [Source:HGNC Symbol;Acc:HGNC:14977]","synonyms":"RGS-PX2","biotype":"protein_coding","ncbi_id":"57231","summary":"This gene encodes a member of the sorting nexin family. Members of this family have a phox (PX) phosphoinositide binding domain and are involved in intracellular trafficking. The encoded protein also contains a regulator of G protein signaling (RGS) domain. Regulator of G protein signaling family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. Alternate splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":85505496,"end":85594156,"strand":-1,"description":"sorting nexin 14 [Source:HGNC Symbol;Acc:HGNC:14977]"}, {"versioned_ensembl_gene_id":"ENSG00000177590.7","gene_symbol":"GIMAP3P","gene_name":"GTPase, IMAP family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:30975]","synonyms":"IAN4P,GIMAP3","biotype":"processed_pseudogene","ncbi_id":"474345","summary":null,"start":150746893,"end":150747728,"strand":-1,"description":"GTPase, IMAP family member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:30975]"}, {"versioned_ensembl_gene_id":"ENSG00000236592.5","gene_symbol":"S100A11P2","gene_name":"S100 calcium binding protein A11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37840]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347701","summary":null,"start":35169224,"end":35169535,"strand":1,"description":"S100 calcium binding protein A11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37840]"}, {"versioned_ensembl_gene_id":"ENSG00000259821.1","gene_symbol":"AC018845.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47004513,"end":47035385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149679.11","gene_symbol":"CABLES2","gene_name":"Cdk5 and Abl enzyme substrate 2 [Source:HGNC Symbol;Acc:HGNC:16143]","synonyms":"ik3-2,dJ908M14.2,C20orf150","biotype":"protein_coding","ncbi_id":"81928","summary":null,"start":62388632,"end":62407285,"strand":-1,"description":"Cdk5 and Abl enzyme substrate 2 [Source:HGNC Symbol;Acc:HGNC:16143]"}, {"versioned_ensembl_gene_id":"ENSG00000267797.1","gene_symbol":"NRBF2P1","gene_name":"nuclear receptor binding factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44604]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648532","summary":null,"start":35841759,"end":35842617,"strand":1,"description":"nuclear receptor binding factor 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44604]"}, {"versioned_ensembl_gene_id":"ENSG00000240720.7","gene_symbol":"LRRD1","gene_name":"leucine rich repeats and death domain containing 1 [Source:HGNC Symbol;Acc:HGNC:34300]","synonyms":"IMAGE:4798971","biotype":"protein_coding","ncbi_id":"401387","summary":null,"start":92112159,"end":92179531,"strand":-1,"description":"leucine rich repeats and death domain containing 1 [Source:HGNC Symbol;Acc:HGNC:34300]"}, {"versioned_ensembl_gene_id":"ENSG00000241822.3","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"C6orf21,LY6G6D,G6f,NG32","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31697642,"end":31701354,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000147874.10","gene_symbol":"HAUS6","gene_name":"HAUS augmin like complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25948]","synonyms":"KIAA1574,FLJ20060,FAM29A,dgt6","biotype":"protein_coding","ncbi_id":"54801","summary":"The protein encoded by this gene is a subunit of the augmin complex. The augmin complex plays a role in microtubule attachment to the kinetochore and central spindle formation. This protein may have a role in efficient chromosome congression and segregation by promoting microtubule-dependent microtubule amplification. Pseudogenes of this gene are located on chromosomes 7 and 20. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":19053143,"end":19103119,"strand":-1,"description":"HAUS augmin like complex subunit 6 [Source:HGNC Symbol;Acc:HGNC:25948]"}, {"versioned_ensembl_gene_id":"ENSG00000215007.3","gene_symbol":"DNAJA1P3","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39339]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644588","summary":null,"start":107351650,"end":107352843,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39339]"}, {"versioned_ensembl_gene_id":"ENSG00000239519.1","gene_symbol":"CADM2-AS1","gene_name":"CADM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41248]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874038","summary":null,"start":85992183,"end":86028007,"strand":-1,"description":"CADM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41248]"}, {"versioned_ensembl_gene_id":"ENSG00000107745.18","gene_symbol":"MICU1","gene_name":"mitochondrial calcium uptake 1 [Source:HGNC Symbol;Acc:HGNC:1530]","synonyms":"CBARA1,CALC,FLJ12684,EFHA3","biotype":"protein_coding","ncbi_id":"10367","summary":"This gene encodes an essential regulator of mitochondrial Ca2+ uptake under basal conditions. The encoded protein interacts with the mitochondrial calcium uniporter, a mitochondrial inner membrane Ca2+ channel, and is essential in preventing mitochondrial Ca2+ overload, which can cause excessive production of reactive oxygen species and cell stress. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2013]","start":72367327,"end":72626191,"strand":-1,"description":"mitochondrial calcium uptake 1 [Source:HGNC Symbol;Acc:HGNC:1530]"}, {"versioned_ensembl_gene_id":"ENSG00000203462.2","gene_symbol":"AC093392.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":56322804,"end":56323601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263368.1","gene_symbol":"AC069366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27526386,"end":27527223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266872.1","gene_symbol":"AC015688.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27625484,"end":27626438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279247.3","gene_symbol":"AK6","gene_name":"adenylate kinase 6 [Source:HGNC Symbol;Acc:HGNC:49151]","synonyms":"CINAP","biotype":"protein_coding","ncbi_id":"102157402","summary":"This gene encodes a protein that belongs to the adenylate kinase family of enzymes. The protein has a nuclear localization and contains Walker A (P-loop) and Walker B motifs and a metal-coordinating residue. The protein may be involved in regulation of Cajal body formation. In human, AK6 and TAF9 (GeneID: 6880) are two distinct genes that share 5' exons. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":69350995,"end":69370027,"strand":-1,"description":"adenylate kinase 6 [Source:HGNC Symbol;Acc:HGNC:49151]"}, {"versioned_ensembl_gene_id":"ENSG00000226849.1","gene_symbol":"AL109811.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11068471,"end":11073097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233577.6","gene_symbol":"AL022332.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25279529,"end":25282674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266965.1","gene_symbol":"AC090220.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":35595901,"end":35597599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279298.1","gene_symbol":"Z99916.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25251523,"end":25252602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164749.11","gene_symbol":"HNF4G","gene_name":"hepatocyte nuclear factor 4 gamma [Source:HGNC Symbol;Acc:HGNC:5026]","synonyms":"NR2A2","biotype":"protein_coding","ncbi_id":"3174","summary":null,"start":75407914,"end":75566843,"strand":1,"description":"hepatocyte nuclear factor 4 gamma [Source:HGNC Symbol;Acc:HGNC:5026]"}, {"versioned_ensembl_gene_id":"ENSG00000273983.1","gene_symbol":"HIST1H3G","gene_name":"histone cluster 1 H3 family member g [Source:HGNC Symbol;Acc:HGNC:4772]","synonyms":"H3/h,H3FH","biotype":"protein_coding","ncbi_id":"8355","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26269405,"end":26271815,"strand":-1,"description":"histone cluster 1 H3 family member g [Source:HGNC Symbol;Acc:HGNC:4772]"}, {"versioned_ensembl_gene_id":"ENSG00000228409.6","gene_symbol":"CCT6P1","gene_name":"chaperonin containing TCP1 subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33094]","synonyms":"CCT6AP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643253","summary":null,"start":65751142,"end":65763354,"strand":1,"description":"chaperonin containing TCP1 subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33094]"}, {"versioned_ensembl_gene_id":"ENSG00000281422.1","gene_symbol":"AC136687.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22363371,"end":22363650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225030.1","gene_symbol":"AL355483.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53291791,"end":53292138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280335.1","gene_symbol":"AC016866.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":49013106,"end":49013819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253135.1","gene_symbol":"AC103724.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42128774,"end":42129249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266905.1","gene_symbol":"AC114684.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48962951,"end":48963941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275663.1","gene_symbol":"HIST1H4G","gene_name":"histone cluster 1 H4 family member g [Source:HGNC Symbol;Acc:HGNC:4792]","synonyms":"H4FL,H4/l","biotype":"protein_coding","ncbi_id":"8369","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26246681,"end":26246977,"strand":-1,"description":"histone cluster 1 H4 family member g [Source:HGNC Symbol;Acc:HGNC:4792]"}, {"versioned_ensembl_gene_id":"ENSG00000173852.14","gene_symbol":"DPY19L1","gene_name":"dpy-19 like 1 [Source:HGNC Symbol;Acc:HGNC:22205]","synonyms":"KIAA0877","biotype":"protein_coding","ncbi_id":"23333","summary":null,"start":34928876,"end":35038271,"strand":-1,"description":"dpy-19 like 1 [Source:HGNC Symbol;Acc:HGNC:22205]"}, {"versioned_ensembl_gene_id":"ENSG00000171858.17","gene_symbol":"RPS21","gene_name":"ribosomal protein S21 [Source:HGNC Symbol;Acc:HGNC:10409]","synonyms":"S21","biotype":"protein_coding","ncbi_id":"6227","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S21E family of ribosomal proteins. It is located in the cytoplasm. Alternative splice variants that encode different protein isoforms have been described, but their existence has not been verified. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":62387116,"end":62388520,"strand":1,"description":"ribosomal protein S21 [Source:HGNC Symbol;Acc:HGNC:10409]"}, {"versioned_ensembl_gene_id":"ENSG00000271947.1","gene_symbol":"AC017076.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6905724,"end":6906301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152642.10","gene_symbol":"GPD1L","gene_name":"glycerol-3-phosphate dehydrogenase 1 like [Source:HGNC Symbol;Acc:HGNC:28956]","synonyms":"KIAA0089","biotype":"protein_coding","ncbi_id":"23171","summary":"The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]","start":32105689,"end":32168713,"strand":1,"description":"glycerol-3-phosphate dehydrogenase 1 like [Source:HGNC Symbol;Acc:HGNC:28956]"}, {"versioned_ensembl_gene_id":"ENSG00000256690.1","gene_symbol":"AP001160.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62832234,"end":62834043,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240572.1","gene_symbol":"AC107297.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99326377,"end":99326552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237344.7","gene_symbol":"PBX2","gene_name":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]","synonyms":"HOX12,G17,PBX2MHC","biotype":"protein_coding","ncbi_id":"5089","summary":"This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]","start":32133204,"end":32138654,"strand":-1,"description":"PBX homeobox 2 [Source:HGNC Symbol;Acc:HGNC:8633]"}, {"versioned_ensembl_gene_id":"ENSG00000283982.1","gene_symbol":"AL445623.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23500691,"end":23672387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241981.2","gene_symbol":"AF213884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102662611,"end":102663073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225978.3","gene_symbol":"HAR1A","gene_name":"highly accelerated region 1A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33117]","synonyms":"NCRNA00064,LINC00064,HAR1F","biotype":"lincRNA","ncbi_id":"768096","summary":null,"start":63102205,"end":63104386,"strand":1,"description":"highly accelerated region 1A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:33117]"}, {"versioned_ensembl_gene_id":"ENSG00000233906.1","gene_symbol":"AL445623.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23671788,"end":23672399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227607.2","gene_symbol":"SUMO2P2","gene_name":"SUMO2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39012]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100859924","summary":null,"start":23632106,"end":23632360,"strand":1,"description":"SUMO2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39012]"}, {"versioned_ensembl_gene_id":"ENSG00000228759.1","gene_symbol":"FAF2P1","gene_name":"Fas associated factor family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45172]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128043","summary":null,"start":91765899,"end":91767196,"strand":-1,"description":"Fas associated factor family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45172]"}, {"versioned_ensembl_gene_id":"ENSG00000254340.1","gene_symbol":"AC022784.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9141424,"end":9145435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174827.13","gene_symbol":"PDZK1","gene_name":"PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:8821]","synonyms":"PDZD1,NHERF3","biotype":"protein_coding","ncbi_id":"5174","summary":"This gene encodes a PDZ domain-containing scaffolding protein. PDZ domain-containing molecules bind to and mediate the subcellular localization of target proteins. The encoded protein mediates the localization of cell surface proteins and plays a critical role in cholesterol metabolism by regulating the HDL receptor, scavenger receptor class B type 1. Single nucleotide polymorphisms in this gene may be associated with metabolic syndrome, and overexpression of this gene may play a role in drug resistance of multiple myeloma. Pseudogenes of this gene are located on the long arm of chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]","start":145670852,"end":145708148,"strand":-1,"description":"PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:8821]"}, {"versioned_ensembl_gene_id":"ENSG00000185186.8","gene_symbol":"LINC00313","gene_name":"long intergenic non-protein coding RNA 313 [Source:HGNC Symbol;Acc:HGNC:16416]","synonyms":"NCRNA00313,C21orf84","biotype":"lincRNA","ncbi_id":"114038","summary":null,"start":43462094,"end":43479534,"strand":-1,"description":"long intergenic non-protein coding RNA 313 [Source:HGNC Symbol;Acc:HGNC:16416]"}, {"versioned_ensembl_gene_id":"ENSG00000241132.7","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"C6orf19,G5b","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31745397,"end":31749825,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000029559.6","gene_symbol":"IBSP","gene_name":"integrin binding sialoprotein [Source:HGNC Symbol;Acc:HGNC:5341]","synonyms":"SP-II,BSP-II,BSP","biotype":"protein_coding","ncbi_id":"3381","summary":"The protein encoded by this gene is a major structural protein of the bone matrix. It constitutes approximately 12% of the noncollagenous proteins in human bone and is synthesized by skeletal-associated cell types, including hypertrophic chondrocytes, osteoblasts, osteocytes, and osteoclasts. The only extraskeletal site of its synthesis is the trophoblast. This protein binds to calcium and hydroxyapatite via its acidic amino acid clusters, and mediates cell attachment through an RGD sequence that recognizes the vitronectin receptor. [provided by RefSeq, Jul 2008]","start":87799581,"end":87812435,"strand":1,"description":"integrin binding sialoprotein [Source:HGNC Symbol;Acc:HGNC:5341]"}, {"versioned_ensembl_gene_id":"ENSG00000232858.1","gene_symbol":"RPL34P27","gene_name":"ribosomal protein L34 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"651249","summary":null,"start":24988577,"end":24988925,"strand":-1,"description":"ribosomal protein L34 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36369]"}, {"versioned_ensembl_gene_id":"ENSG00000273451.1","gene_symbol":"AL031666.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47348137,"end":47349142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277981.1","gene_symbol":"AL731556.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":77738246,"end":77739015,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080618.13","gene_symbol":"CPB2","gene_name":"carboxypeptidase B2 [Source:HGNC Symbol;Acc:HGNC:2300]","synonyms":"CPU,TAFI,PCPB","biotype":"protein_coding","ncbi_id":"1361","summary":"Carboxypeptidases are enzymes that hydrolyze C-terminal peptide bonds. The carboxypeptidase family includes metallo-, serine, and cysteine carboxypeptidases. According to their substrate specificity, these enzymes are referred to as carboxypeptidase A (cleaving aliphatic residues) or carboxypeptidase B (cleaving basic amino residues). The protein encoded by this gene is activated by trypsin and acts on carboxypeptidase B substrates. After thrombin activation, the mature protein downregulates fibrinolysis. Polymorphisms have been described for this gene and its promoter region. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]","start":46053186,"end":46105076,"strand":-1,"description":"carboxypeptidase B2 [Source:HGNC Symbol;Acc:HGNC:2300]"}, {"versioned_ensembl_gene_id":"ENSG00000197935.6","gene_symbol":"ZNF311","gene_name":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]","synonyms":null,"biotype":"protein_coding","ncbi_id":"282890","summary":null,"start":28994785,"end":29005316,"strand":-1,"description":"zinc finger protein 311 [Source:HGNC Symbol;Acc:HGNC:13847]"}, {"versioned_ensembl_gene_id":"ENSG00000232352.1","gene_symbol":"SEMA3B-AS1","gene_name":"SEMA3B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49096]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928931","summary":null,"start":50266641,"end":50267371,"strand":-1,"description":"SEMA3B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49096]"}, {"versioned_ensembl_gene_id":"ENSG00000261992.2","gene_symbol":"GATAD2B","gene_name":"GATA zinc finger domain containing 2B [Source:HGNC Symbol;Acc:HGNC:30778]","synonyms":"P66beta","biotype":"protein_coding","ncbi_id":"57459","summary":"This gene encodes a zinc finger protein transcriptional repressor. The encoded protein is part of the methyl-CpG-binding protein-1 complex, which represses gene expression by deacetylating methylated nucleosomes. Mutations in this gene are linked to intellectual disability and dysmorphic features associated with cognitive disability. [provided by RefSeq, Jun 2016]","start":153821956,"end":153845579,"strand":-1,"description":"GATA zinc finger domain containing 2B [Source:HGNC Symbol;Acc:HGNC:30778]"}, {"versioned_ensembl_gene_id":"ENSG00000188992.11","gene_symbol":"LIPI","gene_name":"lipase I [Source:HGNC Symbol;Acc:HGNC:18821]","synonyms":"PRED5,PLA1C,mPA-PLA1beta,LPDL,CT17","biotype":"protein_coding","ncbi_id":"149998","summary":"The protein encoded by this gene is a phospholipase that hydrolyzes phosphatidic acid to produce lysophosphatidic acid. Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia. This gene is also expressed at high levels in Ewing family tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":14108813,"end":14210891,"strand":-1,"description":"lipase I [Source:HGNC Symbol;Acc:HGNC:18821]"}, {"versioned_ensembl_gene_id":"ENSG00000261786.1","gene_symbol":"AC006058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44117299,"end":44122365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212866.6","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31817974,"end":31820498,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000259657.1","gene_symbol":"PIGHP1","gene_name":"phosphatidylinositol glycan anchor biosynthesis class H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45152]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644761","summary":null,"start":59676757,"end":59677321,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45152]"}, {"versioned_ensembl_gene_id":"ENSG00000280913.2","gene_symbol":"CTSLP2","gene_name":"cathepsin L pseudogene 2 [Source:NCBI gene;Acc:1517]","synonyms":"CTSLL7,bA144G6.6,CTSLP5,CTSLL5,CTSLL7,CTSLL2,CTSLL5,CTSL1P7,CTSLL2,CTSL1P5,CTSL1P7,CTSL1P2,CTSL1P5,bA342C24.4,CTSLP7,CTSL1P2,bA144G6.6,CTSLP5,bA342C24.4,CTSLP7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1517","summary":null,"start":46753605,"end":46759740,"strand":1,"description":"cathepsin L pseudogene 2 [Source:NCBI gene;Acc:1517]"}, {"versioned_ensembl_gene_id":"ENSG00000263181.6","gene_symbol":"CYP2D7","gene_name":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]","synonyms":"CYP2D7P,CYP2D,CYP2D@,CYP2D7P1","biotype":"polymorphic_pseudogene","ncbi_id":"1564","summary":"This gene is a member of the cytochrome P450 gene superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is a segregating pseudogene, where some individuals may have an allele that encodes a functional enzyme, while other individuals have an allele encoding a protein that is predicted to be non-functional. In this case, the functional allele is thought to be rare. This locus is part of a cluster of cytochrome P450 genes on chromosome 22. [provided by RefSeq, Jan 2017]","start":42128051,"end":42132425,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]"}, {"versioned_ensembl_gene_id":"ENSG00000257758.1","gene_symbol":"KRT18P20","gene_name":"keratin 18 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:33388]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"121054","summary":null,"start":104976749,"end":104978027,"strand":-1,"description":"keratin 18 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:33388]"}, {"versioned_ensembl_gene_id":"ENSG00000140299.11","gene_symbol":"BNIP2","gene_name":"BCL2 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:1083]","synonyms":"Nip2,BNIP-2","biotype":"protein_coding","ncbi_id":"663","summary":"This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":59659146,"end":59689534,"strand":-1,"description":"BCL2 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:1083]"}, {"versioned_ensembl_gene_id":"ENSG00000280435.1","gene_symbol":"AC006058.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44115818,"end":44117487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265366.6","gene_symbol":"GLUD1P2","gene_name":"glutamate dehydrogenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4337]","synonyms":"GLUDP2,GLUD1P7,bA342C24.3,GLUDP7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46759019,"end":46786770,"strand":-1,"description":"glutamate dehydrogenase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4337]"}, {"versioned_ensembl_gene_id":"ENSG00000231056.1","gene_symbol":"LINC02522","gene_name":"long intergenic non-protein coding RNA 2522 [Source:HGNC Symbol;Acc:HGNC:53541]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928106","summary":null,"start":10474500,"end":10478502,"strand":-1,"description":"long intergenic non-protein coding RNA 2522 [Source:HGNC Symbol;Acc:HGNC:53541]"}, {"versioned_ensembl_gene_id":"ENSG00000241666.2","gene_symbol":"AL031733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167627385,"end":167630674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276915.1","gene_symbol":"AL109618.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6220330,"end":6220759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198771.10","gene_symbol":"RCSD1","gene_name":"RCSD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28310]","synonyms":"MK2S4,MGC21854,CapZIP","biotype":"protein_coding","ncbi_id":"92241","summary":null,"start":167630093,"end":167706249,"strand":1,"description":"RCSD domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28310]"}, {"versioned_ensembl_gene_id":"ENSG00000229876.1","gene_symbol":"CASC20","gene_name":"cancer susceptibility 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49477]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929244","summary":null,"start":6446723,"end":6528459,"strand":1,"description":"cancer susceptibility 20 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49477]"}, {"versioned_ensembl_gene_id":"ENSG00000090339.8","gene_symbol":"ICAM1","gene_name":"intercellular adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:5344]","synonyms":"CD54,BB2","biotype":"protein_coding","ncbi_id":"3383","summary":"This gene encodes a cell surface glycoprotein which is typically expressed on endothelial cells and cells of the immune system. It binds to integrins of type CD11a / CD18, or CD11b / CD18 and is also exploited by Rhinovirus as a receptor. [provided by RefSeq, Jul 2008]","start":10270835,"end":10286615,"strand":1,"description":"intercellular adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:5344]"}, {"versioned_ensembl_gene_id":"ENSG00000282590.1","gene_symbol":"AC012676.8","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4432481,"end":4433062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231492.2","gene_symbol":"AP003774.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64420391,"end":64432670,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282374.1","gene_symbol":"AC012676.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4435161,"end":4435346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137547.8","gene_symbol":"MRPL15","gene_name":"mitochondrial ribosomal protein L15 [Source:HGNC Symbol;Acc:HGNC:14054]","synonyms":"RPML7,MRP-L7,MRP-L15,L15mt,HSPC145","biotype":"protein_coding","ncbi_id":"29088","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the EcoL15 ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 15q. [provided by RefSeq, Jul 2008]","start":54135210,"end":54147901,"strand":1,"description":"mitochondrial ribosomal protein L15 [Source:HGNC Symbol;Acc:HGNC:14054]"}, {"versioned_ensembl_gene_id":"ENSG00000105371.8","gene_symbol":"ICAM4","gene_name":"intercellular adhesion molecule 4 (Landsteiner-Wiener blood group) [Source:HGNC Symbol;Acc:HGNC:5347]","synonyms":"CD242,LW","biotype":"protein_coding","ncbi_id":"3386","summary":"This gene encodes the Landsteiner-Wiener (LW) blood group antigen(s) that belongs to the immunoglobulin (Ig) superfamily, and that shares similarity with the intercellular adhesion molecule (ICAM) protein family. This ICAM protein contains 2 Ig-like C2-type domains and binds to the leukocyte adhesion LFA-1 protein. The molecular basis of the LW(A)/LW(B) blood group antigens is a single aa variation at position 100; Gln-100=LW(A) and Arg-100=LW(B). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":10286967,"end":10288522,"strand":1,"description":"intercellular adhesion molecule 4 (Landsteiner-Wiener blood group) [Source:HGNC Symbol;Acc:HGNC:5347]"}, {"versioned_ensembl_gene_id":"ENSG00000227700.1","gene_symbol":"AC239809.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":148246169,"end":148246685,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233103.1","gene_symbol":"AL133329.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42047883,"end":42054836,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224335.2","gene_symbol":"AC239809.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148234273,"end":148234489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133627.17","gene_symbol":"ACTR3B","gene_name":"ARP3 actin related protein 3 homolog B [Source:HGNC Symbol;Acc:HGNC:17256]","synonyms":"ARP3beta,ARP11","biotype":"protein_coding","ncbi_id":"57180","summary":"This gene encodes a member of the actin-related proteins (ARP), which form multiprotein complexes and share 35-55% amino acid identity with conventional actin. The protein encoded by this gene may have a regulatory role in the actin cytoskeleton and induce cell-shape change and motility. Pseudogenes of this gene are located on chromosomes 2, 4, 10, 16, 22 and Y. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]","start":152759749,"end":152855378,"strand":1,"description":"ARP3 actin related protein 3 homolog B [Source:HGNC Symbol;Acc:HGNC:17256]"}, {"versioned_ensembl_gene_id":"ENSG00000228847.1","gene_symbol":"ATP5G2P4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42188]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654480","summary":null,"start":42098754,"end":42099173,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42188]"}, {"versioned_ensembl_gene_id":"ENSG00000232265.7","gene_symbol":"AC239803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148162360,"end":148186630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136010.13","gene_symbol":"ALDH1L2","gene_name":"aldehyde dehydrogenase 1 family member L2 [Source:HGNC Symbol;Acc:HGNC:26777]","synonyms":"mtFDH,FLJ38508","biotype":"protein_coding","ncbi_id":"160428","summary":"This gene encodes a member of both the aldehyde dehydrogenase superfamily and the formyl transferase superfamily. This member is the mitochondrial form of 10-formyltetrahydrofolate dehydrogenase (FDH), which converts 10-formyltetrahydrofolate to tetrahydrofolate and CO2 in an NADP(+)-dependent reaction, and plays an essential role in the distribution of one-carbon groups between the cytosolic and mitochondrial compartments of the cell. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2010]","start":105019784,"end":105084577,"strand":-1,"description":"aldehyde dehydrogenase 1 family member L2 [Source:HGNC Symbol;Acc:HGNC:26777]"}, {"versioned_ensembl_gene_id":"ENSG00000228780.2","gene_symbol":"Z92545.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42150511,"end":42150744,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260889.1","gene_symbol":"CKBP1","gene_name":"creatine kinase B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1993]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1157","summary":null,"start":46842632,"end":46844618,"strand":-1,"description":"creatine kinase B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1993]"}, {"versioned_ensembl_gene_id":"ENSG00000241319.1","gene_symbol":"SETP6","gene_name":"SET pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419178","summary":null,"start":81612238,"end":81612805,"strand":-1,"description":"SET pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42925]"}, {"versioned_ensembl_gene_id":"ENSG00000261725.1","gene_symbol":"AC007225.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46850999,"end":46851254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114480.12","gene_symbol":"GBE1","gene_name":"1,4-alpha-glucan branching enzyme 1 [Source:HGNC Symbol;Acc:HGNC:4180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2632","summary":"The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). [provided by RefSeq, Jul 2008]","start":81489699,"end":81762161,"strand":-1,"description":"1,4-alpha-glucan branching enzyme 1 [Source:HGNC Symbol;Acc:HGNC:4180]"}, {"versioned_ensembl_gene_id":"ENSG00000283737.1","gene_symbol":"AL023875.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":42285130,"end":42285925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276125.4","gene_symbol":"CCL4L2","gene_name":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9560","summary":"This gene is one of several cytokine genes that are clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins that function in inflammatory and immunoregulatory processes. The protein encoded by this family member is similar to the chemokine (C-C motif) ligand 4 product, which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals, where most individuals have one to five copies. This gene copy contains a non-consensus splice acceptor site at the 3' terminal exon found in other highly similar gene copies, and it thus uses other alternative splice sites for the 3' terminal exon, resulting in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":36211296,"end":36213250,"strand":1,"description":"C-C motif chemokine ligand 4 like 2 [Source:HGNC Symbol;Acc:HGNC:24066]"}, {"versioned_ensembl_gene_id":"ENSG00000163161.12","gene_symbol":"ERCC3","gene_name":"ERCC excision repair 3, TFIIH core complex helicase subunit [Source:HGNC Symbol;Acc:HGNC:3435]","synonyms":"BTF2,XPB,TFIIH,RAD25,GTF2H","biotype":"protein_coding","ncbi_id":"2071","summary":"This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":127257290,"end":127294176,"strand":-1,"description":"ERCC excision repair 3, TFIIH core complex helicase subunit [Source:HGNC Symbol;Acc:HGNC:3435]"}, {"versioned_ensembl_gene_id":"ENSG00000231772.5","gene_symbol":"Z93403.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42252459,"end":42699385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237107.3","gene_symbol":"AL591473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42499710,"end":42500022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231688.1","gene_symbol":"RPL21P43","gene_name":"ribosomal protein L21 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36008]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271163","summary":null,"start":168858659,"end":168859130,"strand":-1,"description":"ribosomal protein L21 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:36008]"}, {"versioned_ensembl_gene_id":"ENSG00000227678.7","gene_symbol":"AL355581.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130133410,"end":130146179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183604.14","gene_symbol":"SMG1P5","gene_name":"SMG1P5, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49862]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"595101","summary":null,"start":30267553,"end":30335374,"strand":-1,"description":"SMG1P5, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49862]"}, {"versioned_ensembl_gene_id":"ENSG00000181908.5","gene_symbol":"AP003774.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64449074,"end":64451657,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236204.5","gene_symbol":"LINC01376","gene_name":"long intergenic non-protein coding RNA 1376 [Source:HGNC Symbol;Acc:HGNC:50637]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400945","summary":null,"start":18986451,"end":19346748,"strand":-1,"description":"long intergenic non-protein coding RNA 1376 [Source:HGNC Symbol;Acc:HGNC:50637]"}, {"versioned_ensembl_gene_id":"ENSG00000099994.10","gene_symbol":"SUSD2","gene_name":"sushi domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30667]","synonyms":"FLJ22778,BK65A6.2","biotype":"protein_coding","ncbi_id":"56241","summary":null,"start":24181259,"end":24189110,"strand":1,"description":"sushi domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30667]"}, {"versioned_ensembl_gene_id":"ENSG00000268388.5","gene_symbol":"FENDRR","gene_name":"FOXF1 adjacent non-coding developmental regulatory RNA [Source:HGNC Symbol;Acc:HGNC:43894]","synonyms":"lincFOXF1,FOXF1-AS1,onco-lncRNA-21","biotype":"lincRNA","ncbi_id":"400550","summary":"This gene produces a spliced long non-coding RNA transcribed bidirectionally with FOXF1 on the opposite strand. A similar gene in mouse is essential for normal development of the heart and body wall. The encoded transcript is thought to act by binding to polycomb repressive complex 2 (PRC2) and/or TrxG/MLL complexes to promote the methylation of the promoters of target genes, thus reducing their expression. It has been suggested that this transcript may play a role in the progression of gastric cancer. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]","start":86474529,"end":86509099,"strand":-1,"description":"FOXF1 adjacent non-coding developmental regulatory RNA [Source:HGNC Symbol;Acc:HGNC:43894]"}, {"versioned_ensembl_gene_id":"ENSG00000260737.5","gene_symbol":"LINC01227","gene_name":"long intergenic non-protein coding RNA 1227 [Source:HGNC Symbol;Acc:HGNC:49680]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928276","summary":null,"start":80566794,"end":80572808,"strand":-1,"description":"long intergenic non-protein coding RNA 1227 [Source:HGNC Symbol;Acc:HGNC:49680]"}, {"versioned_ensembl_gene_id":"ENSG00000047621.11","gene_symbol":"C12orf4","gene_name":"chromosome 12 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1184]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57102","summary":"This gene is highly conserved from nematodes to humans. In rat, the orthologous gene encodes a cytoplasmic protein that is involved in mast cell degranulation. The human gene has been implicated in autosomal recessive intellectual disability. [provided by RefSeq, Sep 2016]","start":4487728,"end":4538508,"strand":-1,"description":"chromosome 12 open reading frame 4 [Source:HGNC Symbol;Acc:HGNC:1184]"}, {"versioned_ensembl_gene_id":"ENSG00000143867.6","gene_symbol":"OSR1","gene_name":"odd-skipped related transciption factor 1 [Source:HGNC Symbol;Acc:HGNC:8111]","synonyms":"ODD","biotype":"protein_coding","ncbi_id":"130497","summary":null,"start":19351485,"end":19358653,"strand":-1,"description":"odd-skipped related transciption factor 1 [Source:HGNC Symbol;Acc:HGNC:8111]"}, {"versioned_ensembl_gene_id":"ENSG00000237868.1","gene_symbol":"AC097533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122077840,"end":122078318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088386.16","gene_symbol":"SLC15A1","gene_name":"solute carrier family 15 member 1 [Source:HGNC Symbol;Acc:HGNC:10920]","synonyms":"PEPT1,HPEPT1,HPECT1","biotype":"protein_coding","ncbi_id":"6564","summary":"This gene encodes an intestinal hydrogen peptide cotransporter that is a member of the solute carrier family 15. The encoded protein is localized to the brush border membrane of the intestinal epithelium and mediates the uptake of di- and tripeptides from the lumen into the enterocytes. This protein plays an important role in the uptake and digestion of dietary proteins. This protein also facilitates the absorption of numerous peptidomimetic drugs. [provided by RefSeq, Apr 2010]","start":98683801,"end":98752654,"strand":-1,"description":"solute carrier family 15 member 1 [Source:HGNC Symbol;Acc:HGNC:10920]"}, {"versioned_ensembl_gene_id":"ENSG00000232500.1","gene_symbol":"AP005273.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64500853,"end":64505386,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276030.1","gene_symbol":"AC073534.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24146701,"end":24147081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268442.1","gene_symbol":"AC073534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24162370,"end":24163425,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211778.2","gene_symbol":"TRAV4","gene_name":"T-cell receptor alpha variable 4 [Source:HGNC Symbol;Acc:HGNC:12140]","synonyms":"TCRAV4S1,TCRAV20S1","biotype":"TR_V_gene","ncbi_id":"28689","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21736152,"end":21736982,"strand":1,"description":"T-cell receptor alpha variable 4 [Source:HGNC Symbol;Acc:HGNC:12140]"}, {"versioned_ensembl_gene_id":"ENSG00000267696.6","gene_symbol":"ERVK-28","gene_name":"endogenous retrovirus group K member 28 [Source:HGNC Symbol;Acc:HGNC:44981]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106707175","summary":null,"start":27638483,"end":27646483,"strand":-1,"description":"endogenous retrovirus group K member 28 [Source:HGNC Symbol;Acc:HGNC:44981]"}, {"versioned_ensembl_gene_id":"ENSG00000171365.15","gene_symbol":"CLCN5","gene_name":"chloride voltage-gated channel 5 [Source:HGNC Symbol;Acc:HGNC:2023]","synonyms":"XRN,XLRH,NPHL2,NPHL1,hClC-K2,hCIC-K2,DENTS,CLC5,ClC-5","biotype":"protein_coding","ncbi_id":"1184","summary":"This gene encodes a member of the ClC family of chloride ion channels and ion transporters. The encoded protein is primarily localized to endosomal membranes and may function to facilitate albumin uptake by the renal proximal tubule. Mutations in this gene have been found in Dent disease and renal tubular disorders complicated by nephrolithiasis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]","start":49922615,"end":50099235,"strand":1,"description":"chloride voltage-gated channel 5 [Source:HGNC Symbol;Acc:HGNC:2023]"}, {"versioned_ensembl_gene_id":"ENSG00000279882.1","gene_symbol":"AC112702.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":27639300,"end":27639665,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102055.6","gene_symbol":"PPP1R2P9","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:16324]","synonyms":"I-4","biotype":"protein_coding","ncbi_id":"80316","summary":null,"start":42777368,"end":42778247,"strand":-1,"description":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:16324]"}, {"versioned_ensembl_gene_id":"ENSG00000103241.6","gene_symbol":"FOXF1","gene_name":"forkhead box F1 [Source:HGNC Symbol;Acc:HGNC:3809]","synonyms":"FREAC1,FKHL5","biotype":"protein_coding","ncbi_id":"2294","summary":"This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the regulation of pulmonary genes as well as embryonic development. [provided by RefSeq, Jul 2008]","start":86510527,"end":86515418,"strand":1,"description":"forkhead box F1 [Source:HGNC Symbol;Acc:HGNC:3809]"}, {"versioned_ensembl_gene_id":"ENSG00000254054.2","gene_symbol":"AC087273.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17905756,"end":17907887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253215.1","gene_symbol":"AC087273.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17882043,"end":17882661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240404.2","gene_symbol":"AC017015.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81612790,"end":81613075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273073.1","gene_symbol":"AC073869.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":131461821,"end":131463615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137804.12","gene_symbol":"NUSAP1","gene_name":"nucleolar and spindle associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18538]","synonyms":"Q0310,PRO0310p1,NuSAP1,LNP,FLJ13421,BM037,ANKT,SAPL","biotype":"protein_coding","ncbi_id":"51203","summary":"NUSAP1 is a nucleolar-spindle-associated protein that plays a role in spindle microtubule organization (Raemaekers et al., 2003 [PubMed 12963707]).[supplied by OMIM, Jun 2009]","start":41332694,"end":41381050,"strand":1,"description":"nucleolar and spindle associated protein 1 [Source:HGNC Symbol;Acc:HGNC:18538]"}, {"versioned_ensembl_gene_id":"ENSG00000104760.16","gene_symbol":"FGL1","gene_name":"fibrinogen like 1 [Source:HGNC Symbol;Acc:HGNC:3695]","synonyms":"HFREP-1","biotype":"protein_coding","ncbi_id":"2267","summary":"Fibrinogen-like 1 is a member of the fibrinogen family. This protein is homologous to the carboxy terminus of the fibrinogen beta- and gamma- subunits which contains the four conserved cysteines of fibrinogens and fibrinogen related proteins. However, this protein lacks the platelet-binding site, cross-linking region and a thrombin-sensitive site which are necessary for fibrin clot formation. This protein may play a role in the development of hepatocellular carcinomas. Four alternatively spliced transcript variants encoding the same protein exist for this gene. [provided by RefSeq, Jul 2008]","start":17864380,"end":17910365,"strand":-1,"description":"fibrinogen like 1 [Source:HGNC Symbol;Acc:HGNC:3695]"}, {"versioned_ensembl_gene_id":"ENSG00000228149.1","gene_symbol":"RPL3P1","gene_name":"ribosomal protein L3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10352]","synonyms":"RPL3P","biotype":"processed_pseudogene","ncbi_id":"8488","summary":null,"start":36168970,"end":36170180,"strand":-1,"description":"ribosomal protein L3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10352]"}, {"versioned_ensembl_gene_id":"ENSG00000163002.12","gene_symbol":"NUP35","gene_name":"nucleoporin 35 [Source:HGNC Symbol;Acc:HGNC:29797]","synonyms":"MP44","biotype":"protein_coding","ncbi_id":"129401","summary":"This gene encodes a member of the nucleoporin family. The encoded protein contains two membrane binding regions, is localized to the nuclear rim, and is part of the nuclear pore complex. All molecules entering or leaving the nucleus either diffuse through or are actively transported by the nuclear pore complex. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 7 and 10. [provided by RefSeq, Dec 2013]","start":183117513,"end":183161680,"strand":1,"description":"nucleoporin 35 [Source:HGNC Symbol;Acc:HGNC:29797]"}, {"versioned_ensembl_gene_id":"ENSG00000142197.12","gene_symbol":"DOPEY2","gene_name":"dopey family member 2 [Source:HGNC Symbol;Acc:HGNC:1291]","synonyms":"KIAA0933,C21orf5","biotype":"protein_coding","ncbi_id":"9980","summary":null,"start":36156782,"end":36294274,"strand":1,"description":"dopey family member 2 [Source:HGNC Symbol;Acc:HGNC:1291]"}, {"versioned_ensembl_gene_id":"ENSG00000263238.1","gene_symbol":"CTSO","gene_name":"cathepsin O [Source:HGNC Symbol;Acc:HGNC:2542]","synonyms":"CTSO1","biotype":"protein_coding","ncbi_id":"1519","summary":"The protein encoded by the gene is a cysteine proteinase and a member of the papain superfamily. This proteolytic enzyme is involved in cellular protein degradation and turnover. The recombinant form of this enzyme was shown to degrade synthetic peptides typically used as substrates for cysteine proteinases and its proteolytic activity was abolished by an inhibitor of cyteine proteinase. [provided by RefSeq, Jul 2008]","start":155924118,"end":155953911,"strand":-1,"description":"cathepsin O [Source:HGNC Symbol;Acc:HGNC:2542]"}, {"versioned_ensembl_gene_id":"ENSG00000151131.10","gene_symbol":"C12orf45","gene_name":"chromosome 12 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:28628]","synonyms":"MGC40397","biotype":"protein_coding","ncbi_id":"121053","summary":null,"start":104986310,"end":105074197,"strand":1,"description":"chromosome 12 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:28628]"}, {"versioned_ensembl_gene_id":"ENSG00000188130.13","gene_symbol":"MAPK12","gene_name":"mitogen-activated protein kinase 12 [Source:HGNC Symbol;Acc:HGNC:6874]","synonyms":"SAPK3,SAPK-3,PRKM12,p38gamma,ERK6","biotype":"protein_coding","ncbi_id":"6300","summary":"Activation of members of the mitogen-activated protein kinase family is a major mechanism for transduction of extracellular signals. Stress-activated protein kinases are one subclass of MAP kinases. The protein encoded by this gene functions as a signal transducer during differentiation of myoblasts to myotubes. [provided by RefSeq, Jul 2008]","start":50245450,"end":50261825,"strand":-1,"description":"mitogen-activated protein kinase 12 [Source:HGNC Symbol;Acc:HGNC:6874]"}, {"versioned_ensembl_gene_id":"ENSG00000181019.12","gene_symbol":"NQO1","gene_name":"NAD(P)H quinone dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:2874]","synonyms":"QR1,NMOR1,DTD,DIA4,DHQU","biotype":"protein_coding","ncbi_id":"1728","summary":"This gene is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a cytoplasmic 2-electron reductase. This FAD-binding protein forms homodimers and reduces quinones to hydroquinones. This protein's enzymatic activity prevents the one electron reduction of quinones that results in the production of radical species. Mutations in this gene have been associated with tardive dyskinesia (TD), an increased risk of hematotoxicity after exposure to benzene, and susceptibility to various forms of cancer. Altered expression of this protein has been seen in many tumors and is also associated with Alzheimer's disease (AD). Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":69706996,"end":69726951,"strand":-1,"description":"NAD(P)H quinone dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:2874]"}, {"versioned_ensembl_gene_id":"ENSG00000267607.1","gene_symbol":"AC011511.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10285801,"end":10289019,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266978.1","gene_symbol":"AC011511.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10252268,"end":10285108,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158863.21","gene_symbol":"FAM160B2","gene_name":"family with sequence similarity 160 member B2 [Source:HGNC Symbol;Acc:HGNC:16492]","synonyms":"RAI16,FLJ21801","biotype":"protein_coding","ncbi_id":"64760","summary":null,"start":22089159,"end":22104898,"strand":1,"description":"family with sequence similarity 160 member B2 [Source:HGNC Symbol;Acc:HGNC:16492]"}, {"versioned_ensembl_gene_id":"ENSG00000267105.1","gene_symbol":"AC011511.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10259109,"end":10260045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153015.15","gene_symbol":"CWC27","gene_name":"CWC27 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:10664]","synonyms":"SDCCAG10,SDCCAG-10,NY-CO-10","biotype":"protein_coding","ncbi_id":"10283","summary":null,"start":64768930,"end":65018763,"strand":1,"description":"CWC27 spliceosome associated protein homolog [Source:HGNC Symbol;Acc:HGNC:10664]"}, {"versioned_ensembl_gene_id":"ENSG00000105364.13","gene_symbol":"MRPL4","gene_name":"mitochondrial ribosomal protein L4 [Source:HGNC Symbol;Acc:HGNC:14276]","synonyms":"CGI-28","biotype":"protein_coding","ncbi_id":"51073","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Sequence analysis identified alternatively spliced variants that encode different protein isoforms. [provided by RefSeq, Jul 2008]","start":10251901,"end":10260045,"strand":1,"description":"mitochondrial ribosomal protein L4 [Source:HGNC Symbol;Acc:HGNC:14276]"}, {"versioned_ensembl_gene_id":"ENSG00000223771.3","gene_symbol":"SUMO2P1","gene_name":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]","synonyms":"SMT3H2P,dJ271M21,SUMO2P,SMT3Bp","biotype":"processed_pseudogene","ncbi_id":"285829","summary":null,"start":29632655,"end":29632938,"strand":-1,"description":"SUMO2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13985]"}, {"versioned_ensembl_gene_id":"ENSG00000275387.1","gene_symbol":"AL049732.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54842014,"end":54842134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173769.4","gene_symbol":"TOPAZ1","gene_name":"testis and ovary specific PAZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24746]","synonyms":"FLJ36157,C3orf77","biotype":"protein_coding","ncbi_id":"375337","summary":null,"start":44241886,"end":44332098,"strand":1,"description":"testis and ovary specific PAZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24746]"}, {"versioned_ensembl_gene_id":"ENSG00000219870.2","gene_symbol":"AC119618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9179385,"end":9179606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228543.1","gene_symbol":"AC003684.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9249920,"end":9275206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232111.2","gene_symbol":"AC073488.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9402751,"end":9404802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279511.1","gene_symbol":"AL356274.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37142967,"end":37146718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258285.1","gene_symbol":"TESC-AS1","gene_name":"TESC antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51142]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928244","summary":null,"start":117099481,"end":117142091,"strand":1,"description":"TESC antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:51142]"}, {"versioned_ensembl_gene_id":"ENSG00000213492.2","gene_symbol":"NT5C3AP1","gene_name":"5'-nucleotidase, cytosolic IIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18530]","synonyms":"UMPH1P,NT5C3P1","biotype":"transcribed_processed_pseudogene","ncbi_id":"90859","summary":null,"start":117574512,"end":117576174,"strand":-1,"description":"5'-nucleotidase, cytosolic IIIA pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18530]"}, {"versioned_ensembl_gene_id":"ENSG00000276470.1","gene_symbol":"NPPA-AS1_1","gene_name":"NPPA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02156]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11843812,"end":11843984,"strand":1,"description":"NPPA antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02156]"}, {"versioned_ensembl_gene_id":"ENSG00000276025.2","gene_symbol":"OR5P2","gene_name":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]","synonyms":"JCG3","biotype":"protein_coding","ncbi_id":"120065","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7795905,"end":7796973,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]"}, {"versioned_ensembl_gene_id":"ENSG00000125730.16","gene_symbol":"C3","gene_name":"complement C3 [Source:HGNC Symbol;Acc:HGNC:1318]","synonyms":"CPAMD1,C3b,C3a,ARMD9","biotype":"protein_coding","ncbi_id":"718","summary":"Complement component C3 plays a central role in the activation of complement system. Its activation is required for both classical and alternative complement activation pathways. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form the mature protein, which is then further processed to generate numerous peptide products. The C3a peptide, also known as the C3a anaphylatoxin, modulates inflammation and possesses antimicrobial activity. Mutations in this gene are associated with atypical hemolytic uremic syndrome and age-related macular degeneration in human patients. [provided by RefSeq, Nov 2015]","start":6677704,"end":6730562,"strand":-1,"description":"complement C3 [Source:HGNC Symbol;Acc:HGNC:1318]"}, {"versioned_ensembl_gene_id":"ENSG00000236922.9","gene_symbol":"LINC01378","gene_name":"long intergenic non-protein coding RNA 1378 [Source:HGNC Symbol;Acc:HGNC:50645]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103689918","summary":null,"start":117406166,"end":117691188,"strand":1,"description":"long intergenic non-protein coding RNA 1378 [Source:HGNC Symbol;Acc:HGNC:50645]"}, {"versioned_ensembl_gene_id":"ENSG00000230283.1","gene_symbol":"RPS12P24","gene_name":"ribosomal protein S12 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271551","summary":null,"start":37220860,"end":37221246,"strand":-1,"description":"ribosomal protein S12 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:35561]"}, {"versioned_ensembl_gene_id":"ENSG00000272157.1","gene_symbol":"AC107373.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24956621,"end":24957110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125975.13","gene_symbol":"C20orf173","gene_name":"chromosome 20 open reading frame 173 [Source:HGNC Symbol;Acc:HGNC:16166]","synonyms":"dJ477O4.4","biotype":"protein_coding","ncbi_id":"140873","summary":null,"start":35523186,"end":35529652,"strand":-1,"description":"chromosome 20 open reading frame 173 [Source:HGNC Symbol;Acc:HGNC:16166]"}, {"versioned_ensembl_gene_id":"ENSG00000269813.1","gene_symbol":"AC010336.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7959123,"end":7960012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277586.2","gene_symbol":"NEFL","gene_name":"neurofilament light [Source:HGNC Symbol;Acc:HGNC:7739]","synonyms":"PPP1R110,NFL,NF68,CMT2E,CMT1F","biotype":"protein_coding","ncbi_id":"4747","summary":"Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y. [provided by RefSeq, Oct 2008]","start":24950955,"end":24957110,"strand":-1,"description":"neurofilament light [Source:HGNC Symbol;Acc:HGNC:7739]"}, {"versioned_ensembl_gene_id":"ENSG00000066044.14","gene_symbol":"ELAVL1","gene_name":"ELAV like RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3312]","synonyms":"MelG,HUR,Hua","biotype":"protein_coding","ncbi_id":"1994","summary":"The protein encoded by this gene is a member of the ELAVL family of RNA-binding proteins that contain several RNA recognition motifs, and selectively bind AU-rich elements (AREs) found in the 3' untranslated regions of mRNAs. AREs signal degradation of mRNAs as a means to regulate gene expression, thus by binding AREs, the ELAVL family of proteins play a role in stabilizing ARE-containing mRNAs. This gene has been implicated in a variety of biological processes and has been linked to a number of diseases, including cancer. It is highly expressed in many cancers, and could be potentially useful in cancer diagnosis, prognosis, and therapy. [provided by RefSeq, Sep 2012]","start":7958579,"end":8005659,"strand":-1,"description":"ELAV like RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3312]"}, {"versioned_ensembl_gene_id":"ENSG00000237684.1","gene_symbol":"RPSAP35","gene_name":"ribosomal protein SA pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36447]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270916","summary":null,"start":117413462,"end":117414279,"strand":1,"description":"ribosomal protein SA pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36447]"}, {"versioned_ensembl_gene_id":"ENSG00000234597.1","gene_symbol":"AC010096.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19458220,"end":19468961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088876.11","gene_symbol":"ZNF343","gene_name":"zinc finger protein 343 [Source:HGNC Symbol;Acc:HGNC:16017]","synonyms":"MGC10715","biotype":"protein_coding","ncbi_id":"79175","summary":null,"start":2481817,"end":2524702,"strand":-1,"description":"zinc finger protein 343 [Source:HGNC Symbol;Acc:HGNC:16017]"}, {"versioned_ensembl_gene_id":"ENSG00000259335.1","gene_symbol":"HNRNPMP1","gene_name":"heterogeneous nuclear ribonucleoprotein M pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48745]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645204","summary":null,"start":44447577,"end":44449344,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein M pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48745]"}, {"versioned_ensembl_gene_id":"ENSG00000140297.12","gene_symbol":"GCNT3","gene_name":"glucosaminyl (N-acetyl) transferase 3, mucin type [Source:HGNC Symbol;Acc:HGNC:4205]","synonyms":"C2GnT2,C2GnT-M,C2/4GnT","biotype":"protein_coding","ncbi_id":"9245","summary":"This gene encodes a member of the N-acetylglucosaminyltransferase family. The encoded protein is a beta-6-N-acetylglucosamine-transferase that catalyzes the formation of core 2 and core 4 O-glycans on mucin-type glycoproteins.[provided by RefSeq, Apr 2009]","start":59594875,"end":59640239,"strand":1,"description":"glucosaminyl (N-acetyl) transferase 3, mucin type [Source:HGNC Symbol;Acc:HGNC:4205]"}, {"versioned_ensembl_gene_id":"ENSG00000134265.12","gene_symbol":"NAPG","gene_name":"NSF attachment protein gamma [Source:HGNC Symbol;Acc:HGNC:7642]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8774","summary":"This gene encodes soluble NSF attachment protein gamma. The soluble NSF attachment proteins (SNAPs) enable N-ethyl-maleimide-sensitive fusion protein (NSF) to bind to target membranes. NSF and SNAPs appear to be general components of the intracellular membrane fusion apparatus, and their action at specific sites of fusion must be controlled by SNAP receptors particular to the membranes being fused. The product of this gene mediates platelet exocytosis and controls the membrane fusion events of this process.[provided by RefSeq, Dec 2008]","start":10525905,"end":10552761,"strand":1,"description":"NSF attachment protein gamma [Source:HGNC Symbol;Acc:HGNC:7642]"}, {"versioned_ensembl_gene_id":"ENSG00000259563.1","gene_symbol":"AC025430.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44516650,"end":44517483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172728.15","gene_symbol":"FUT10","gene_name":"fucosyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:19234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84750","summary":null,"start":33370824,"end":33473422,"strand":-1,"description":"fucosyltransferase 10 [Source:HGNC Symbol;Acc:HGNC:19234]"}, {"versioned_ensembl_gene_id":"ENSG00000237838.1","gene_symbol":"AC092422.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24687919,"end":25174305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137770.13","gene_symbol":"CTDSPL2","gene_name":"CTD small phosphatase like 2 [Source:HGNC Symbol;Acc:HGNC:26936]","synonyms":"FLJ10523,HSPC129","biotype":"protein_coding","ncbi_id":"51496","summary":null,"start":44427234,"end":44529038,"strand":1,"description":"CTD small phosphatase like 2 [Source:HGNC Symbol;Acc:HGNC:26936]"}, {"versioned_ensembl_gene_id":"ENSG00000130775.15","gene_symbol":"THEMIS2","gene_name":"thymocyte selection associated family member 2 [Source:HGNC Symbol;Acc:HGNC:16839]","synonyms":"ICB-1,C1orf38","biotype":"protein_coding","ncbi_id":"9473","summary":null,"start":27872543,"end":27886685,"strand":1,"description":"thymocyte selection associated family member 2 [Source:HGNC Symbol;Acc:HGNC:16839]"}, {"versioned_ensembl_gene_id":"ENSG00000242507.6","gene_symbol":"FO393401.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35520852,"end":35528255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185437.13","gene_symbol":"SH3BGR","gene_name":"SH3 domain binding glutamate rich protein [Source:HGNC Symbol;Acc:HGNC:10822]","synonyms":"21-GARP","biotype":"protein_coding","ncbi_id":"6450","summary":null,"start":39445855,"end":39515506,"strand":1,"description":"SH3 domain binding glutamate rich protein [Source:HGNC Symbol;Acc:HGNC:10822]"}, {"versioned_ensembl_gene_id":"ENSG00000103671.9","gene_symbol":"TRIP4","gene_name":"thyroid hormone receptor interactor 4 [Source:HGNC Symbol;Acc:HGNC:12310]","synonyms":"ZC2HC5,HsT17391","biotype":"protein_coding","ncbi_id":"9325","summary":"This gene encodes a subunit of the tetrameric nuclear activating signal cointegrator 1 (ASC-1) complex, which associates with transcriptional coactivators, nuclear receptors and basal transcription factors to facilitate nuclear receptors-mediated transcription. This protein is localized in the nucleus and contains an E1A-type zinc finger domain, which mediates interaction with transcriptional coactivators and ligand-bound nuclear receptors, such as thyroid hormone receptor and retinoid X receptor alpha, but not glucocorticoid receptor. Mutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1). [provided by RefSeq, Apr 2016]","start":64387748,"end":64455303,"strand":1,"description":"thyroid hormone receptor interactor 4 [Source:HGNC Symbol;Acc:HGNC:12310]"}, {"versioned_ensembl_gene_id":"ENSG00000111877.17","gene_symbol":"MCM9","gene_name":"minichromosome maintenance 9 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:21484]","synonyms":"MGC35304,MCMDC1,FLJ20170,dJ329L24.3,C6orf61","biotype":"protein_coding","ncbi_id":"254394","summary":"The protein encoded by this gene is a member of the mini-chromosome maintenance (MCM) protein family that are essential for the initiation of eukaryotic genome replication. Binding of this protein to chromatin has been shown to be a pre-requisite for recruiting the MCM2-7 helicase to DNA replication origins. This protein also binds, and is a positive regulator of, the chromatin licensing and DNA replication factor 1, CDT1. [provided by RefSeq, Nov 2010]","start":118813442,"end":118935162,"strand":-1,"description":"minichromosome maintenance 9 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:21484]"}, {"versioned_ensembl_gene_id":"ENSG00000228482.1","gene_symbol":"LINC01713","gene_name":"long intergenic non-protein coding RNA 1713 [Source:HGNC Symbol;Acc:HGNC:52500]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372516","summary":null,"start":6731258,"end":6736136,"strand":-1,"description":"long intergenic non-protein coding RNA 1713 [Source:HGNC Symbol;Acc:HGNC:52500]"}, {"versioned_ensembl_gene_id":"ENSG00000206380.11","gene_symbol":"C6orf48","gene_name":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]","synonyms":"D6S57,G8","biotype":"protein_coding","ncbi_id":"50854","summary":null,"start":31824855,"end":31830009,"strand":1,"description":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]"}, {"versioned_ensembl_gene_id":"ENSG00000125845.6","gene_symbol":"BMP2","gene_name":"bone morphogenetic protein 2 [Source:HGNC Symbol;Acc:HGNC:1069]","synonyms":"BMP2A","biotype":"protein_coding","ncbi_id":"650","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone and cartilage development. Duplication of a regulatory region downstream of this gene causes a form of brachydactyly characterized by a malformed index finger and second toe in human patients. [provided by RefSeq, Jul 2016]","start":6767664,"end":6780280,"strand":1,"description":"bone morphogenetic protein 2 [Source:HGNC Symbol;Acc:HGNC:1069]"}, {"versioned_ensembl_gene_id":"ENSG00000104228.12","gene_symbol":"TRIM35","gene_name":"tripartite motif containing 35 [Source:HGNC Symbol;Acc:HGNC:16285]","synonyms":"MAIR,KIAA1098,HLS5","biotype":"protein_coding","ncbi_id":"23087","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. [provided by RefSeq, Jul 2008]","start":27284887,"end":27311319,"strand":-1,"description":"tripartite motif containing 35 [Source:HGNC Symbol;Acc:HGNC:16285]"}, {"versioned_ensembl_gene_id":"ENSG00000176054.6","gene_symbol":"RPL23P2","gene_name":"ribosomal protein L23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10324]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"54028","summary":null,"start":28997613,"end":28998033,"strand":-1,"description":"ribosomal protein L23 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:10324]"}, {"versioned_ensembl_gene_id":"ENSG00000173692.12","gene_symbol":"PSMD1","gene_name":"proteasome 26S subunit, non-ATPase 1 [Source:HGNC Symbol;Acc:HGNC:9554]","synonyms":"S1,Rpn2,P112","biotype":"protein_coding","ncbi_id":"5707","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes the largest non-ATPase subunit of the 19S regulator lid, which is responsible for substrate recognition and binding. There is evidence that this proteasome and its subunits interact with viral proteins, including those of coronaviruses. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Aug 2020]","start":231056864,"end":231172827,"strand":1,"description":"proteasome 26S subunit, non-ATPase 1 [Source:HGNC Symbol;Acc:HGNC:9554]"}, {"versioned_ensembl_gene_id":"ENSG00000274130.1","gene_symbol":"AC245128.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237195.1","gene_symbol":"DLGAP5P1","gene_name":"discs large homolog associated protein 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23945]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"360014","summary":null,"start":6158802,"end":6159265,"strand":1,"description":"discs large homolog associated protein 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23945]"}, {"versioned_ensembl_gene_id":"ENSG00000275112.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000140307.10","gene_symbol":"GTF2A2","gene_name":"general transcription factor IIA subunit 2 [Source:HGNC Symbol;Acc:HGNC:4647]","synonyms":"TFIIA,HsT18745","biotype":"protein_coding","ncbi_id":"2958","summary":"Accurate transcription initiation on TATA-containing class II genes involves the ordered assembly of RNA polymerase II (POLR2A; MIM 180660) and the general initiation factors TFIIA, TFIIB (MIM 189963), TFIID (MIM 313650), TFIIE (MIM 189962), TFIIF (MIM 189968), TFIIG/TFIIJ, and TFIIH (MIM 189972). The first step involves recognition of the TATA element by the TATA-binding subunit (TBP; MIM 600075) and may be regulated by TFIIA, a factor that interacts with both TBP and a TBP-associated factor (TAF; MIM 600475) in TFIID. TFIIA has 2 subunits (43 and 12 kD) in yeast and 3 subunits in higher eukaryotes. In HeLa extracts, it consists of a 35-kD alpha subunit and a 19-kD beta subunit encoded by the N- and C-terminal regions of GTF2A1 (MIM 600520), respectively, and a 12-kD gamma subunit encoded by GTF2A2 (DeJong et al., 1995 [PubMed 7724559]).[supplied by OMIM, Mar 2008]","start":59638062,"end":59657541,"strand":-1,"description":"general transcription factor IIA subunit 2 [Source:HGNC Symbol;Acc:HGNC:4647]"}, {"versioned_ensembl_gene_id":"ENSG00000141431.10","gene_symbol":"ASXL3","gene_name":"additional sex combs like 3, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29357]","synonyms":"KIAA1713","biotype":"protein_coding","ncbi_id":"80816","summary":"This gene encodes a protein containing a plant homeodomain (PHD) zinc finger domain that plays a role in the regulation of gene transcription. The encoded protein has been shown to negatively regulate lipogenesis by binding to and inhibiting the transcriptional activity of two nuclear hormone receptors, oxysterols receptor LXR-alpha (LXRalpha) and thyroid hormone receptor beta (TRbeta). The encoded protein may also inhibit histone deubiquitination. Mutations in this gene have been identified in human patients with Bainbridge-Ropers syndrome, which is characterized by feeding difficulties, developmental delay and other features. [provided by RefSeq, May 2017]","start":33578577,"end":33751192,"strand":1,"description":"additional sex combs like 3, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29357]"}, {"versioned_ensembl_gene_id":"ENSG00000179407.3","gene_symbol":"DNAJB8","gene_name":"DnaJ heat shock protein family (Hsp40) member B8 [Source:HGNC Symbol;Acc:HGNC:23699]","synonyms":"MGC33884,CT156","biotype":"protein_coding","ncbi_id":"165721","summary":"The protein encoded by this gene belongs to the DNAJ/HSP40 family of proteins that regulate chaperone activity. This family member suppresses aggregation and toxicity of polyglutamine proteins, and the C-terminal tail is essential for this activity. It has been implicated as a cancer-testis antigen and as a cancer stem-like cell antigen involved in renal cell carcinoma. [provided by RefSeq, Jun 2012]","start":128462439,"end":128467248,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B8 [Source:HGNC Symbol;Acc:HGNC:23699]"}, {"versioned_ensembl_gene_id":"ENSG00000242049.1","gene_symbol":"DNAJB8-AS1","gene_name":"DNAJB8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41029]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285224","summary":null,"start":128463594,"end":128472317,"strand":1,"description":"DNAJB8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41029]"}, {"versioned_ensembl_gene_id":"ENSG00000234043.3","gene_symbol":"NUDT9P1","gene_name":"nudix hydrolase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28523]","synonyms":"MGC34007,C10orf98,bA56M3.1","biotype":"processed_pseudogene","ncbi_id":"119369","summary":null,"start":91152605,"end":91153349,"strand":-1,"description":"nudix hydrolase 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28523]"}, {"versioned_ensembl_gene_id":"ENSG00000114423.18","gene_symbol":"CBLB","gene_name":"Cbl proto-oncogene B [Source:HGNC Symbol;Acc:HGNC:1542]","synonyms":"Cbl-b,RNF56","biotype":"protein_coding","ncbi_id":"868","summary":"This gene encodes an E3 ubiquitin-protein ligase which promotes proteosome-mediated protein degradation by transferring ubiquitin from an E2 ubiquitin-conjugating enzyme to a substrate. The encoded protein is involved in the regulation of immune response by limiting T-cell receptor, B-cell receptor, and high affinity immunoglobulin epsilon receptor activation. Studies in mouse suggest that this gene is involved in antifungal host defense and that its inhibition leads to increased fungal killing. Manipulation of this gene may be beneficial in implementing immunotherapies for a variety of conditions, including cancer, autoimmune diseases, allergies, and infections. [provided by RefSeq, Sep 2017]","start":105655461,"end":105869552,"strand":-1,"description":"Cbl proto-oncogene B [Source:HGNC Symbol;Acc:HGNC:1542]"}, {"versioned_ensembl_gene_id":"ENSG00000171557.16","gene_symbol":"FGG","gene_name":"fibrinogen gamma chain [Source:HGNC Symbol;Acc:HGNC:3694]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2266","summary":"The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":154604134,"end":154612967,"strand":-1,"description":"fibrinogen gamma chain [Source:HGNC Symbol;Acc:HGNC:3694]"}, {"versioned_ensembl_gene_id":"ENSG00000230177.1","gene_symbol":"AL080317.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111277932,"end":111278742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270280.1","gene_symbol":"AL451086.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43000174,"end":43000396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236830.6","gene_symbol":"CBR3-AS1","gene_name":"CBR3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43664]","synonyms":"PlncRNA-1","biotype":"processed_transcript","ncbi_id":"100506428","summary":null,"start":36131767,"end":36175815,"strand":-1,"description":"CBR3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43664]"}, {"versioned_ensembl_gene_id":"ENSG00000254061.1","gene_symbol":"AC091144.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33436268,"end":33436700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224294.1","gene_symbol":"PINCR","gene_name":"p53-induced noncoding RNA [Source:HGNC Symbol;Acc:HGNC:53590]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927501","summary":null,"start":43176994,"end":43226598,"strand":1,"description":"p53-induced noncoding RNA [Source:HGNC Symbol;Acc:HGNC:53590]"}, {"versioned_ensembl_gene_id":"ENSG00000198042.10","gene_symbol":"MAK16","gene_name":"MAK16 homolog [Source:HGNC Symbol;Acc:HGNC:13703]","synonyms":"RBM13,MAK16L","biotype":"protein_coding","ncbi_id":"84549","summary":null,"start":33484750,"end":33501260,"strand":1,"description":"MAK16 homolog [Source:HGNC Symbol;Acc:HGNC:13703]"}, {"versioned_ensembl_gene_id":"ENSG00000273749.4","gene_symbol":"CYFIP1","gene_name":"cytoplasmic FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13759]","synonyms":"KIAA0068,SHYC,P140SRA-1","biotype":"protein_coding","ncbi_id":"23191","summary":"This gene encodes a protein that regulates cytoskeletal dynamics and protein translation. The encoded protein is a component of the WAVE regulatory complex (WRC), which promotes actin polymerization.This protein also interacts with the Fragile X mental retardation protein (FMRP) and translation initiation factor 4E to inhibit protein translation. A large chromosomal deletion including this gene is associated with increased risk of schizophrenia and epilepsy in human patients. Reduced expression of this gene has been observed in various human cancers and the encoded protein may inhibit tumor invasion. [provided by RefSeq, May 2017]","start":22867052,"end":22981063,"strand":-1,"description":"cytoplasmic FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:13759]"}, {"versioned_ensembl_gene_id":"ENSG00000237206.1","gene_symbol":"IMPDH1P4","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33959]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139334","summary":null,"start":43278125,"end":43279658,"strand":-1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:33959]"}, {"versioned_ensembl_gene_id":"ENSG00000125971.16","gene_symbol":"DYNLRB1","gene_name":"dynein light chain roadblock-type 1 [Source:HGNC Symbol;Acc:HGNC:15468]","synonyms":"ROBLD1,DNLC2A,DNCL2A","biotype":"protein_coding","ncbi_id":"83658","summary":"This gene is a member of the roadblock dynein light chain family. The encoded cytoplasmic protein is capable of binding intermediate chain proteins, interacts with transforming growth factor-beta, and has been implicated in the regulation of actin modulating proteins. Upregulation of this gene has been associated with hepatocellular carcinomas, suggesting that this gene may be involved in tumor progression. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 12 and 18. [provided by RefSeq, Aug 2013]","start":34516409,"end":34540958,"strand":1,"description":"dynein light chain roadblock-type 1 [Source:HGNC Symbol;Acc:HGNC:15468]"}, {"versioned_ensembl_gene_id":"ENSG00000231750.3","gene_symbol":"NANOGP10","gene_name":"Nanog homeobox pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:23108]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"349372","summary":null,"start":43407665,"end":43408559,"strand":-1,"description":"Nanog homeobox pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:23108]"}, {"versioned_ensembl_gene_id":"ENSG00000266977.1","gene_symbol":"AC006504.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27849730,"end":27889222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267630.1","gene_symbol":"AC005758.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27918943,"end":27929370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180628.14","gene_symbol":"PCGF5","gene_name":"polycomb group ring finger 5 [Source:HGNC Symbol;Acc:HGNC:28264]","synonyms":"RNF159,MGC16202","biotype":"protein_coding","ncbi_id":"84333","summary":null,"start":91163012,"end":91284331,"strand":1,"description":"polycomb group ring finger 5 [Source:HGNC Symbol;Acc:HGNC:28264]"}, {"versioned_ensembl_gene_id":"ENSG00000267768.1","gene_symbol":"AC006504.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27908356,"end":27908554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236487.2","gene_symbol":"AC079168.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24681909,"end":24682634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281468.1","gene_symbol":"AC006504.8","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27802838,"end":27803472,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256566.1","gene_symbol":"AL049650.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2467212,"end":2508907,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253194.1","gene_symbol":"AL365275.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118934785,"end":119031541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267264.1","gene_symbol":"AC006504.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27803538,"end":27804060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267323.1","gene_symbol":"SLC25A1P5","gene_name":"solute carrier family 25 member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642290","summary":null,"start":27805423,"end":27806205,"strand":-1,"description":"solute carrier family 25 member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43849]"}, {"versioned_ensembl_gene_id":"ENSG00000281470.1","gene_symbol":"AC096576.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21704652,"end":21726228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218803.1","gene_symbol":"GSTM2P1","gene_name":"glutathione S-transferase mu 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38009]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442245","summary":null,"start":111046868,"end":111047521,"strand":-1,"description":"glutathione S-transferase mu 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38009]"}, {"versioned_ensembl_gene_id":"ENSG00000259547.1","gene_symbol":"CYCSP2","gene_name":"cytochrome c, somatic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24410]","synonyms":"HCP37","biotype":"processed_pseudogene","ncbi_id":"360183","summary":null,"start":41108878,"end":41109178,"strand":1,"description":"cytochrome c, somatic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24410]"}, {"versioned_ensembl_gene_id":"ENSG00000100053.9","gene_symbol":"CRYBB3","gene_name":"crystallin beta B3 [Source:HGNC Symbol;Acc:HGNC:2400]","synonyms":"CRYB3","biotype":"protein_coding","ncbi_id":"1417","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta basic group member, is part of a gene cluster with beta-A4, beta-B1, and beta-B2. Mutations in this gene result in cataract congenital nuclear autosomal recessive type 2. [provided by RefSeq, Feb 2013]","start":25199850,"end":25207363,"strand":1,"description":"crystallin beta B3 [Source:HGNC Symbol;Acc:HGNC:2400]"}, {"versioned_ensembl_gene_id":"ENSG00000267623.3","gene_symbol":"AC005357.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27902595,"end":27984743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280838.1","gene_symbol":"AC210756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21582138,"end":21620924,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125835.18","gene_symbol":"SNRPB","gene_name":"small nuclear ribonucleoprotein polypeptides B and B1 [Source:HGNC Symbol;Acc:HGNC:11153]","synonyms":"SNRPB1,snRNP-B,SmB/SmB',Sm-B/B',COD","biotype":"protein_coding","ncbi_id":"6628","summary":"The protein encoded by this gene is one of several nuclear proteins that are found in common among U1, U2, U4/U6, and U5 small ribonucleoprotein particles (snRNPs). These snRNPs are involved in pre-mRNA splicing, and the encoded protein may also play a role in pre-mRNA splicing or snRNP structure. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding different isoforms (B and B') have been found for this gene. [provided by RefSeq, Jul 2008]","start":2461634,"end":2470853,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptides B and B1 [Source:HGNC Symbol;Acc:HGNC:11153]"}, {"versioned_ensembl_gene_id":"ENSG00000111879.18","gene_symbol":"FAM184A","gene_name":"family with sequence similarity 184 member A [Source:HGNC Symbol;Acc:HGNC:20991]","synonyms":"FLJ13942,C6orf60","biotype":"protein_coding","ncbi_id":"79632","summary":null,"start":118959763,"end":119149387,"strand":-1,"description":"family with sequence similarity 184 member A [Source:HGNC Symbol;Acc:HGNC:20991]"}, {"versioned_ensembl_gene_id":"ENSG00000281758.1","gene_symbol":"KCNIP4","gene_name":"potassium voltage-gated channel interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30083]","synonyms":"MGC44947,KCHIP4,CALP","biotype":"protein_coding","ncbi_id":"80333","summary":"This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have EF-hand-like domains, and differ from each other in the N-terminus. They are integral subunit components of native Kv4 channel complexes. They may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. This protein member also interacts with presenilin. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":21544390,"end":21737314,"strand":-1,"description":"potassium voltage-gated channel interacting protein 4 [Source:HGNC Symbol;Acc:HGNC:30083]"}, {"versioned_ensembl_gene_id":"ENSG00000281559.1","gene_symbol":"AC096576.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21663714,"end":21664071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269925.1","gene_symbol":"Z98884.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":7776383,"end":7776775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261770.1","gene_symbol":"AC006504.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27757184,"end":27760849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272635.1","gene_symbol":"AC006504.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27793488,"end":27984984,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000049245.12","gene_symbol":"VAMP3","gene_name":"vesicle associated membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:12644]","synonyms":"CEB","biotype":"protein_coding","ncbi_id":"9341","summary":"Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. This gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Because of its high homology to other known VAMPs, its broad tissue distribution, and its subcellular localization, the protein encoded by this gene was shown to be the human equivalent of the rodent cellubrevin. In platelets the protein resides on a compartment that is not mobilized to the plasma membrane on calcium or thrombin stimulation. [provided by RefSeq, Jul 2008]","start":7771269,"end":7781432,"strand":1,"description":"vesicle associated membrane protein 3 [Source:HGNC Symbol;Acc:HGNC:12644]"}, {"versioned_ensembl_gene_id":"ENSG00000261304.1","gene_symbol":"LINC02252","gene_name":"long intergenic non-protein coding RNA 2252 [Source:HGNC Symbol;Acc:HGNC:53150]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370762","summary":null,"start":34651135,"end":34655764,"strand":-1,"description":"long intergenic non-protein coding RNA 2252 [Source:HGNC Symbol;Acc:HGNC:53150]"}, {"versioned_ensembl_gene_id":"ENSG00000261824.6","gene_symbol":"LINC00662","gene_name":"long intergenic non-protein coding RNA 662 [Source:HGNC Symbol;Acc:HGNC:27122]","synonyms":null,"biotype":"lincRNA","ncbi_id":"148189","summary":null,"start":27684580,"end":27793940,"strand":-1,"description":"long intergenic non-protein coding RNA 662 [Source:HGNC Symbol;Acc:HGNC:27122]"}, {"versioned_ensembl_gene_id":"ENSG00000230870.2","gene_symbol":"FBXW11P1","gene_name":"F-box and WD repeat domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1145]","synonyms":"FBXW1BP1,FBXW1BP,BTRC2P","biotype":"processed_pseudogene","ncbi_id":"54099","summary":null,"start":31627127,"end":31628600,"strand":-1,"description":"F-box and WD repeat domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1145]"}, {"versioned_ensembl_gene_id":"ENSG00000253832.1","gene_symbol":"AC107373.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24992002,"end":25009777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228628.8","gene_symbol":"ATF6B","gene_name":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]","synonyms":"G13,CREBL1","biotype":"protein_coding","ncbi_id":"1388","summary":"The protein encoded by this gene is a transcription factor in the unfolded protein response (UPR) pathway during ER stress. Either as a homodimer or as a heterodimer with ATF6-alpha, the encoded protein binds to the ER stress response element, interacting with nuclear transcription factor Y to activate UPR target genes. The protein is normally found in the membrane of the endoplasmic reticulum; however, under ER stress, the N-terminal cytoplasmic domain is cleaved from the rest of the protein and translocates to the nucleus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":32191691,"end":32204680,"strand":-1,"description":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]"}, {"versioned_ensembl_gene_id":"ENSG00000282306.1","gene_symbol":"AC073488.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9404954,"end":9405731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278253.1","gene_symbol":"OR5P3","gene_name":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]","synonyms":"JCG1","biotype":"protein_coding","ncbi_id":"120066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7825037,"end":7825972,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]"}, {"versioned_ensembl_gene_id":"ENSG00000275850.1","gene_symbol":"AC005912.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":3171657,"end":3174056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129696.12","gene_symbol":"TTI2","gene_name":"TELO2 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:26262]","synonyms":"FLJ23263,C8orf41","biotype":"protein_coding","ncbi_id":"80185","summary":"This gene encodes a regulator of the DNA damage response. The protein is a component of the Triple T complex (TTT) which also includes telomere length regulation protein and TELO2 interacting protein 1. The TTT complex is involved in cellular resistance to DNA damage stresses and may act as a regulator of phosphoinositide-3-kinase-related protein kinase (PIKK) abundance. [provided by RefSeq, May 2013]","start":33473386,"end":33513601,"strand":-1,"description":"TELO2 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:26262]"}, {"versioned_ensembl_gene_id":"ENSG00000279827.1","gene_symbol":"AC136469.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8444570,"end":8445597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159248.4","gene_symbol":"GJD2","gene_name":"gap junction protein delta 2 [Source:HGNC Symbol;Acc:HGNC:19154]","synonyms":"GJA9,CX36","biotype":"protein_coding","ncbi_id":"57369","summary":"This gene encodes a member of the connexin protein family. Connexins are gap junction proteins which are arranged in groups of 6 around a central pore to form a connexon, a component of the gap junction intercellular channel. The channels formed by this protein allow cationic molecule exchange between human beta cells and may function in the regulation of insulin secretion. [provided by RefSeq, Oct 2012]","start":34751032,"end":34754965,"strand":-1,"description":"gap junction protein delta 2 [Source:HGNC Symbol;Acc:HGNC:19154]"}, {"versioned_ensembl_gene_id":"ENSG00000230390.1","gene_symbol":"LINC01048","gene_name":"long intergenic non-protein coding RNA 1048 [Source:HGNC Symbol;Acc:HGNC:49042]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103695431","summary":null,"start":37481467,"end":37484769,"strand":-1,"description":"long intergenic non-protein coding RNA 1048 [Source:HGNC Symbol;Acc:HGNC:49042]"}, {"versioned_ensembl_gene_id":"ENSG00000159231.5","gene_symbol":"CBR3","gene_name":"carbonyl reductase 3 [Source:HGNC Symbol;Acc:HGNC:1549]","synonyms":"SDR21C2","biotype":"protein_coding","ncbi_id":"874","summary":"Carbonyl reductase 3 catalyzes the reduction of a large number of biologically and pharmacologically active carbonyl compounds to their corresponding alcohols. The enzyme is classified as a monomeric NADPH-dependent oxidoreductase. CBR3 contains three exons spanning 11.2 kilobases and is closely linked to another carbonyl reductase gene - CBR1. [provided by RefSeq, Jul 2008]","start":36134912,"end":36146566,"strand":1,"description":"carbonyl reductase 3 [Source:HGNC Symbol;Acc:HGNC:1549]"}, {"versioned_ensembl_gene_id":"ENSG00000267575.6","gene_symbol":"AC006504.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27793463,"end":27918863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240760.1","gene_symbol":"AC109462.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55352721,"end":55353088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280497.1","gene_symbol":"OR5E1P","gene_name":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]","synonyms":"TPCR24,OR5E1,HSTPCR24","biotype":"unprocessed_pseudogene","ncbi_id":"26343","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7859351,"end":7860277,"strand":1,"description":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]"}, {"versioned_ensembl_gene_id":"ENSG00000275226.1","gene_symbol":"LINC00547","gene_name":"long intergenic non-protein coding RNA 547 [Source:HGNC Symbol;Acc:HGNC:43682]","synonyms":"FLJ34747","biotype":"lincRNA","ncbi_id":"400121","summary":null,"start":37534940,"end":37551536,"strand":1,"description":"long intergenic non-protein coding RNA 547 [Source:HGNC Symbol;Acc:HGNC:43682]"}, {"versioned_ensembl_gene_id":"ENSG00000215045.8","gene_symbol":"GRID2IP","gene_name":"Grid2 interacting protein [Source:HGNC Symbol;Acc:HGNC:18464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392862","summary":"Glutamate receptor delta-2 (GRID2; MIM 602368) is predominantly expressed at parallel fiber-Purkinje cell postsynapses and plays crucial roles in synaptogenesis and synaptic plasticity. GRID2IP1 interacts with GRID2 and may control GRID2 signaling in Purkinje cells (Matsuda et al., 2006 [PubMed 16835239]).[supplied by OMIM, Mar 2008]","start":6497462,"end":6551436,"strand":-1,"description":"Grid2 interacting protein [Source:HGNC Symbol;Acc:HGNC:18464]"}, {"versioned_ensembl_gene_id":"ENSG00000271789.1","gene_symbol":"AL080317.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111297126,"end":111298510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234509.1","gene_symbol":"AP000253.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31653593,"end":31659500,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254219.1","gene_symbol":"AC087439.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":91042690,"end":91044762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274966.1","gene_symbol":"AC019322.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30395146,"end":30396368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233553.1","gene_symbol":"AC108462.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1341044,"end":1346568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281367.2","gene_symbol":"AC044810.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7861399,"end":7916588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183249.8","gene_symbol":"NF1P3","gene_name":"neurofibromin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:7766]","synonyms":"NF1L1","biotype":"unprocessed_pseudogene","ncbi_id":"4764","summary":null,"start":14000927,"end":14005279,"strand":1,"description":"neurofibromin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:7766]"}, {"versioned_ensembl_gene_id":"ENSG00000109738.10","gene_symbol":"GLRB","gene_name":"glycine receptor beta [Source:HGNC Symbol;Acc:HGNC:4329]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2743","summary":"This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":157076057,"end":157172090,"strand":1,"description":"glycine receptor beta [Source:HGNC Symbol;Acc:HGNC:4329]"}, {"versioned_ensembl_gene_id":"ENSG00000214889.3","gene_symbol":"RPS9P1","gene_name":"ribosomal protein S9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10443]","synonyms":"RPS9P","biotype":"processed_pseudogene","ncbi_id":"8410","summary":null,"start":36132450,"end":36133032,"strand":1,"description":"ribosomal protein S9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10443]"}, {"versioned_ensembl_gene_id":"ENSG00000235403.1","gene_symbol":"AC114808.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1059133,"end":1068341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266906.1","gene_symbol":"AC005357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27983032,"end":27983332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233442.2","gene_symbol":"PPP6R2P1","gene_name":"protein phosphatase 6 regulatory subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39605]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100631381","summary":null,"start":14007134,"end":14014880,"strand":1,"description":"protein phosphatase 6 regulatory subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39605]"}, {"versioned_ensembl_gene_id":"ENSG00000267389.2","gene_symbol":"AC006504.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27892495,"end":27898927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172575.11","gene_symbol":"RASGRP1","gene_name":"RAS guanyl releasing protein 1 [Source:HGNC Symbol;Acc:HGNC:9878]","synonyms":"RASGRP,CalDAG-GEFII","biotype":"protein_coding","ncbi_id":"10125","summary":"This gene is a member of a family of genes characterized by the presence of a Ras superfamily guanine nucleotide exchange factor (GEF) domain. It functions as a diacylglycerol (DAG)-regulated nucleotide exchange factor specifically activating Ras through the exchange of bound GDP for GTP. It activates the Erk/MAP kinase cascade and regulates T-cells and B-cells development, homeostasis and differentiation. Alternatively spliced transcript variants encoding different isoforms have been identified. Altered expression of the different isoforms of this protein may be a cause of susceptibility to systemic lupus erythematosus (SLE). [provided by RefSeq, Jul 2008]","start":38488103,"end":38565575,"strand":-1,"description":"RAS guanyl releasing protein 1 [Source:HGNC Symbol;Acc:HGNC:9878]"}, {"versioned_ensembl_gene_id":"ENSG00000242948.1","gene_symbol":"EPS15P1","gene_name":"epidermal growth factor receptor pathway substrate 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18166]","synonyms":"PRO1866,EPS15L2","biotype":"transcribed_processed_pseudogene","ncbi_id":"55380","summary":null,"start":46781373,"end":46783443,"strand":1,"description":"epidermal growth factor receptor pathway substrate 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18166]"}, {"versioned_ensembl_gene_id":"ENSG00000186399.10","gene_symbol":"GOLGA8R","gene_name":"golgin A8 family member R [Source:HGNC Symbol;Acc:HGNC:44407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101059918","summary":null,"start":30403740,"end":30414162,"strand":-1,"description":"golgin A8 family member R [Source:HGNC Symbol;Acc:HGNC:44407]"}, {"versioned_ensembl_gene_id":"ENSG00000278442.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850442,"end":54867200,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000227161.1","gene_symbol":"AC092755.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":59644298,"end":59672302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273724.1","gene_symbol":"AC106782.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30336400,"end":30343336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259238.1","gene_symbol":"AC092755.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59688517,"end":59689418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239254.1","gene_symbol":"AC009220.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":139172516,"end":139174266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226788.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33130117,"end":33134342,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000183960.8","gene_symbol":"KCNH8","gene_name":"potassium voltage-gated channel subfamily H member 8 [Source:HGNC Symbol;Acc:HGNC:18864]","synonyms":"Kv12.1,elk3","biotype":"protein_coding","ncbi_id":"131096","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. [provided by RefSeq, Jul 2008]","start":19148454,"end":19535646,"strand":1,"description":"potassium voltage-gated channel subfamily H member 8 [Source:HGNC Symbol;Acc:HGNC:18864]"}, {"versioned_ensembl_gene_id":"ENSG00000254554.1","gene_symbol":"AC080023.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10302657,"end":10303704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270020.1","gene_symbol":"AC009108.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86520383,"end":86523897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254043.1","gene_symbol":"AC011632.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74891151,"end":74896302,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217950.4","gene_symbol":"NOC2LP2","gene_name":"NOC2 like nucleolar associated transcriptional repressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52286]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401010","summary":null,"start":131442644,"end":131444587,"strand":-1,"description":"NOC2 like nucleolar associated transcriptional repressor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52286]"}, {"versioned_ensembl_gene_id":"ENSG00000243697.1","gene_symbol":"AC009108.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86525457,"end":86526252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156253.6","gene_symbol":"RWDD2B","gene_name":"RWD domain containing 2B [Source:HGNC Symbol;Acc:HGNC:1302]","synonyms":"GL011,C21orf6","biotype":"protein_coding","ncbi_id":"10069","summary":null,"start":29004384,"end":29019378,"strand":-1,"description":"RWD domain containing 2B [Source:HGNC Symbol;Acc:HGNC:1302]"}, {"versioned_ensembl_gene_id":"ENSG00000172554.11","gene_symbol":"SNTG2","gene_name":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]","synonyms":"SYN5,G2SYN","biotype":"protein_coding","ncbi_id":"54221","summary":"This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq, Jul 2008]","start":950868,"end":1367613,"strand":1,"description":"syntrophin gamma 2 [Source:HGNC Symbol;Acc:HGNC:13741]"}, {"versioned_ensembl_gene_id":"ENSG00000272370.1","gene_symbol":"AC092354.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65020038,"end":65020551,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224519.1","gene_symbol":"HMGN1P19","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874445","summary":null,"start":46634614,"end":46634946,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39363]"}, {"versioned_ensembl_gene_id":"ENSG00000162236.11","gene_symbol":"STX5","gene_name":"syntaxin 5 [Source:HGNC Symbol;Acc:HGNC:11440]","synonyms":"STX5A,SED5","biotype":"protein_coding","ncbi_id":"6811","summary":"This gene encodes a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for v-SNAREs (vesicle-SNAP receptors), permitting specific synaptic vesicle docking and fusion. The encoded protein regulates endoplasmic reticulum to Golgi transport and plays a critical role in autophagy. Autoantibodies targeting the encoded protein may be a diagnostic marker for endometriosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":62806897,"end":62832088,"strand":-1,"description":"syntaxin 5 [Source:HGNC Symbol;Acc:HGNC:11440]"}, {"versioned_ensembl_gene_id":"ENSG00000232742.3","gene_symbol":"RHOQP2","gene_name":"ras homolog family member Q pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37836]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730041","summary":null,"start":131460999,"end":131461577,"strand":1,"description":"ras homolog family member Q pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37836]"}, {"versioned_ensembl_gene_id":"ENSG00000272354.1","gene_symbol":"AC092354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65020614,"end":65020989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169217.8","gene_symbol":"CD2BP2","gene_name":"CD2 cytoplasmic tail binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1656]","synonyms":"U5-52K,Snu40,PPP1R59,LIN1","biotype":"protein_coding","ncbi_id":"10421","summary":"This gene encodes a bi-functional protein. In the cytoplasm, the encoded protein binds the cytoplasmic tail of human surface antigen CD2 via its C-terminal GYF domain, and regulate CD2-triggered T lymphocyte activation. In the nucleus, this protein is a component of the U5 small nuclear ribonucleoprotein complex and is involved in RNA splicing. A pseudogene has been identified on chromosome 7. Alternative splicing results in multiple transcript variants but their biological validity has not been determined. [provided by RefSeq, Nov 2008]","start":30350766,"end":30355361,"strand":-1,"description":"CD2 cytoplasmic tail binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1656]"}, {"versioned_ensembl_gene_id":"ENSG00000233539.5","gene_symbol":"AC011294.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46673785,"end":46759851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259326.1","gene_symbol":"AC116158.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38502853,"end":38504981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234794.9","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32446450,"end":32451660,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000232072.1","gene_symbol":"AC004870.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46890625,"end":47049678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179523.4","gene_symbol":"EIF3J-AS1","gene_name":"EIF3J antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48616]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645212","summary":null,"start":44527257,"end":44536923,"strand":-1,"description":"EIF3J antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48616]"}, {"versioned_ensembl_gene_id":"ENSG00000179152.19","gene_symbol":"TCAIM","gene_name":"T-cell activation inhibitor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25241]","synonyms":"TOAG-1,DKFZp313N0621,C3orf23","biotype":"protein_coding","ncbi_id":"285343","summary":null,"start":44338119,"end":44409451,"strand":1,"description":"T-cell activation inhibitor, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25241]"}, {"versioned_ensembl_gene_id":"ENSG00000242552.1","gene_symbol":"MRPL42P4","gene_name":"mitochondrial ribosomal protein L42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29713]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"346470","summary":null,"start":47026128,"end":47026570,"strand":-1,"description":"mitochondrial ribosomal protein L42 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:29713]"}, {"versioned_ensembl_gene_id":"ENSG00000282370.1","gene_symbol":"AC233699.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36225618,"end":36227179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172987.12","gene_symbol":"HPSE2","gene_name":"heparanase 2 (inactive) [Source:HGNC Symbol;Acc:HGNC:18374]","synonyms":"HPA2,UFS,HPR2","biotype":"protein_coding","ncbi_id":"60495","summary":"This gene encodes a heparanase enzyme. The encoded protein is a endoglycosidase that degrades heparin sulfate proteoglycans located on the extracellular matrix and cell surface. This protein may be involved in biological processes involving remodeling of the extracellular matrix including angiogenesis and tumor progression. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","start":98457077,"end":99235862,"strand":-1,"description":"heparanase 2 (inactive) [Source:HGNC Symbol;Acc:HGNC:18374]"}, {"versioned_ensembl_gene_id":"ENSG00000276451.2","gene_symbol":"OR10A6","gene_name":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":7938266,"end":7939295,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]"}, {"versioned_ensembl_gene_id":"ENSG00000214754.3","gene_symbol":"AC004870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47052793,"end":47053674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223829.5","gene_symbol":"AC004870.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46969702,"end":47027481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253738.1","gene_symbol":"OTUD6B-AS1","gene_name":"OTUD6B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50466]","synonyms":"GS1-251I9.4","biotype":"antisense_RNA","ncbi_id":"100506365","summary":null,"start":91059909,"end":91070189,"strand":-1,"description":"OTUD6B antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50466]"}, {"versioned_ensembl_gene_id":"ENSG00000249771.1","gene_symbol":"AC108210.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41883060,"end":41894579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229192.6","gene_symbol":"AC004870.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47000620,"end":47079128,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249887.1","gene_symbol":"AC108210.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41924180,"end":41924380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218186.2","gene_symbol":"KRT8P43","gene_name":"keratin 8 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:39877]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289319","summary":null,"start":24598012,"end":24599790,"strand":1,"description":"keratin 8 pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:39877]"}, {"versioned_ensembl_gene_id":"ENSG00000236100.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30760718,"end":30761447,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000236629.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32685134,"end":32685966,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000273953.1","gene_symbol":"OR10A3","gene_name":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]","synonyms":"HTPCRX12,HSHTPCRX12","biotype":"protein_coding","ncbi_id":"26496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7949167,"end":7950227,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]"}, {"versioned_ensembl_gene_id":"ENSG00000137261.13","gene_symbol":"KIAA0319","gene_name":"KIAA0319 [Source:HGNC Symbol;Acc:HGNC:21580]","synonyms":"NMIG","biotype":"protein_coding","ncbi_id":"9856","summary":"This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":24544104,"end":24646155,"strand":-1,"description":"KIAA0319 [Source:HGNC Symbol;Acc:HGNC:21580]"}, {"versioned_ensembl_gene_id":"ENSG00000234331.1","gene_symbol":"CR753846.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32696518,"end":32697352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278881.2","gene_symbol":"FP325331.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47115838,"end":47117217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253670.1","gene_symbol":"AC073581.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25141394,"end":25141968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280080.2","gene_symbol":"TBC1D22A-AS1","gene_name":"TBC1D22A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51221]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"642757","summary":null,"start":46914092,"end":46916042,"strand":-1,"description":"TBC1D22A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51221]"}, {"versioned_ensembl_gene_id":"ENSG00000277741.4","gene_symbol":"GOLGA6L17P","gene_name":"golgin A6 family-like 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:49414]","synonyms":"GOLGA6L21P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"642402","summary":null,"start":82519590,"end":82526412,"strand":1,"description":"golgin A6 family-like 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:49414]"}, {"versioned_ensembl_gene_id":"ENSG00000276780.2","gene_symbol":"NLRP10","gene_name":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]","synonyms":"Pynod,PAN5,NOD8,NALP10,CLR11.1","biotype":"protein_coding","ncbi_id":"338322","summary":"Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). The protein encoded by this gene belongs to the NALP protein family despite lacking the LRR region. This protein likely plays a regulatory role in the innate immune system. The protein belongs to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. Other experiments indicate that this gene acts as a multifunctional negative regulator of inflammation and apoptosis. [provided by RefSeq, Jul 2008]","start":7970057,"end":7976059,"strand":-1,"description":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]"}, {"versioned_ensembl_gene_id":"ENSG00000261602.1","gene_symbol":"AC092115.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69709874,"end":69710583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275170.1","gene_symbol":"FRG2MP","gene_name":"FSHD region gene 2 family member M, pseudogene [Source:HGNC Symbol;Acc:HGNC:51799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481739","summary":null,"start":14019060,"end":14020725,"strand":-1,"description":"FSHD region gene 2 family member M, pseudogene [Source:HGNC Symbol;Acc:HGNC:51799]"}, {"versioned_ensembl_gene_id":"ENSG00000231596.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205E,DVB,D6S205,DQB3,HLA-DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32709925,"end":32710861,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000054611.13","gene_symbol":"TBC1D22A","gene_name":"TBC1 domain family member 22A [Source:HGNC Symbol;Acc:HGNC:1309]","synonyms":"C22orf4","biotype":"protein_coding","ncbi_id":"25771","summary":null,"start":46762617,"end":47175699,"strand":1,"description":"TBC1 domain family member 22A [Source:HGNC Symbol;Acc:HGNC:1309]"}, {"versioned_ensembl_gene_id":"ENSG00000211779.3","gene_symbol":"TRAV5","gene_name":"T-cell receptor alpha variable 5 [Source:HGNC Symbol;Acc:HGNC:12143]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28688","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21749178,"end":21749705,"strand":1,"description":"T-cell receptor alpha variable 5 [Source:HGNC Symbol;Acc:HGNC:12143]"}, {"versioned_ensembl_gene_id":"ENSG00000271333.1","gene_symbol":"AC019322.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30420283,"end":30420429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183160.8","gene_symbol":"TMEM119","gene_name":"transmembrane protein 119 [Source:HGNC Symbol;Acc:HGNC:27884]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338773","summary":null,"start":108589846,"end":108598320,"strand":-1,"description":"transmembrane protein 119 [Source:HGNC Symbol;Acc:HGNC:27884]"}, {"versioned_ensembl_gene_id":"ENSG00000240954.1","gene_symbol":"RPL4P1","gene_name":"ribosomal protein L4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23551]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"650808","summary":null,"start":21750269,"end":21751546,"strand":1,"description":"ribosomal protein L4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23551]"}, {"versioned_ensembl_gene_id":"ENSG00000211780.3","gene_symbol":"TRAV6","gene_name":"T-cell receptor alpha variable 6 [Source:HGNC Symbol;Acc:HGNC:12144]","synonyms":"TCRAV5S1","biotype":"TR_V_gene","ncbi_id":"6956","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21768489,"end":21769080,"strand":1,"description":"T-cell receptor alpha variable 6 [Source:HGNC Symbol;Acc:HGNC:12144]"}, {"versioned_ensembl_gene_id":"ENSG00000228349.1","gene_symbol":"RPS26P4","gene_name":"ribosomal protein S26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23775]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"692146","summary":null,"start":39491544,"end":39491898,"strand":-1,"description":"ribosomal protein S26 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23775]"}, {"versioned_ensembl_gene_id":"ENSG00000101892.11","gene_symbol":"ATP1B4","gene_name":"ATPase Na+/K+ transporting family member beta 4 [Source:HGNC Symbol;Acc:HGNC:808]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23439","summary":"This gene has been found in all vertebrate genomes sequenced to date. However, this gene has undergone a change in function in placental mammals compared to other species. Specifically, in fish, avian, and amphibian species, this gene encodes plasma membrane-bound beta-subunits of Na,K-ATPase. In placental mammals, the encoded protein interacts with the nuclear transcriptional coregulator SKIP and may be involved in the regulation of TGF-beta signaling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]","start":120362085,"end":120383249,"strand":1,"description":"ATPase Na+/K+ transporting family member beta 4 [Source:HGNC Symbol;Acc:HGNC:808]"}, {"versioned_ensembl_gene_id":"ENSG00000227440.1","gene_symbol":"ATP5G1P4","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39507]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287755","summary":null,"start":172828736,"end":172829176,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39507]"}, {"versioned_ensembl_gene_id":"ENSG00000235225.1","gene_symbol":"AC016712.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":222726457,"end":222726834,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099998.17","gene_symbol":"GGT5","gene_name":"gamma-glutamyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4260]","synonyms":"GGTLA1,GGT-REL","biotype":"protein_coding","ncbi_id":"2687","summary":"This gene is a member of the gamma-glutamyl transpeptidase gene family, and some reports indicate that it is capable of cleaving the gamma-glutamyl moiety of glutathione. The protein encoded by this gene is synthesized as a single, catalytically-inactive polypeptide, that is processed post-transcriptionally to form a heavy and light subunit, with the catalytic activity contained within the small subunit. The encoded enzyme is able to convert leukotriene C4 to leukotriene D4, but appears to have distinct substrate specificity compared to gamma-glutamyl transpeptidase. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":24219654,"end":24245142,"strand":-1,"description":"gamma-glutamyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4260]"}, {"versioned_ensembl_gene_id":"ENSG00000234283.1","gene_symbol":"LINC01731","gene_name":"long intergenic non-protein coding RNA 1731 [Source:HGNC Symbol;Acc:HGNC:52519]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371226","summary":null,"start":148271884,"end":148280749,"strand":-1,"description":"long intergenic non-protein coding RNA 1731 [Source:HGNC Symbol;Acc:HGNC:52519]"}, {"versioned_ensembl_gene_id":"ENSG00000229565.1","gene_symbol":"LINC02264","gene_name":"long intergenic non-protein coding RNA 2264 [Source:HGNC Symbol;Acc:HGNC:53176]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377391","summary":null,"start":117834401,"end":117869948,"strand":1,"description":"long intergenic non-protein coding RNA 2264 [Source:HGNC Symbol;Acc:HGNC:53176]"}, {"versioned_ensembl_gene_id":"ENSG00000230683.1","gene_symbol":"DDTP1","gene_name":"D-dopachrome tautomerase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44546]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060160","summary":null,"start":38515448,"end":38515830,"strand":-1,"description":"D-dopachrome tautomerase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44546]"}, {"versioned_ensembl_gene_id":"ENSG00000282501.1","gene_symbol":"AC073488.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9406025,"end":9406778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125734.15","gene_symbol":"GPR108","gene_name":"G protein-coupled receptor 108 [Source:HGNC Symbol;Acc:HGNC:17829]","synonyms":"LUSTR2","biotype":"protein_coding","ncbi_id":"56927","summary":null,"start":6729914,"end":6737603,"strand":-1,"description":"G protein-coupled receptor 108 [Source:HGNC Symbol;Acc:HGNC:17829]"}, {"versioned_ensembl_gene_id":"ENSG00000211781.3","gene_symbol":"TRAV7","gene_name":"T-cell receptor alpha variable 7 [Source:HGNC Symbol;Acc:HGNC:12145]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28686","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21782993,"end":21783503,"strand":1,"description":"T-cell receptor alpha variable 7 [Source:HGNC Symbol;Acc:HGNC:12145]"}, {"versioned_ensembl_gene_id":"ENSG00000279235.1","gene_symbol":"AC011944.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78906127,"end":78906809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116885.18","gene_symbol":"OSCP1","gene_name":"organic solute carrier partner 1 [Source:HGNC Symbol;Acc:HGNC:29971]","synonyms":"NOR1,C1orf102","biotype":"protein_coding","ncbi_id":"127700","summary":null,"start":36415827,"end":36450451,"strand":-1,"description":"organic solute carrier partner 1 [Source:HGNC Symbol;Acc:HGNC:29971]"}, {"versioned_ensembl_gene_id":"ENSG00000282358.1","gene_symbol":"AC073488.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9406952,"end":9407708,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243822.1","gene_symbol":"AC073522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149357169,"end":149357545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282668.1","gene_symbol":"AC073488.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9407861,"end":9408638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211782.2","gene_symbol":"TRAV8-1","gene_name":"T-cell receptor alpha variable 8-1 [Source:HGNC Symbol;Acc:HGNC:12146]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28685","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21797287,"end":21797886,"strand":1,"description":"T-cell receptor alpha variable 8-1 [Source:HGNC Symbol;Acc:HGNC:12146]"}, {"versioned_ensembl_gene_id":"ENSG00000282299.1","gene_symbol":"AC073488.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9408818,"end":9409571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211783.3","gene_symbol":"TRAV9-1","gene_name":"T-cell receptor alpha variable 9-1 [Source:HGNC Symbol;Acc:HGNC:12153]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28678","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21811502,"end":21811977,"strand":1,"description":"T-cell receptor alpha variable 9-1 [Source:HGNC Symbol;Acc:HGNC:12153]"}, {"versioned_ensembl_gene_id":"ENSG00000204174.7","gene_symbol":"NPY4R","gene_name":"neuropeptide Y receptor Y4 [Source:HGNC Symbol;Acc:HGNC:9329]","synonyms":"Y4,PPYR1,PP1","biotype":"protein_coding","ncbi_id":"5540","summary":null,"start":46461099,"end":46465881,"strand":-1,"description":"neuropeptide Y receptor Y4 [Source:HGNC Symbol;Acc:HGNC:9329]"}, {"versioned_ensembl_gene_id":"ENSG00000255079.1","gene_symbol":"AC104241.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44694863,"end":44696301,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153310.19","gene_symbol":"FAM49B","gene_name":"family with sequence similarity 49 member B [Source:HGNC Symbol;Acc:HGNC:25216]","synonyms":"BM-009","biotype":"protein_coding","ncbi_id":"51571","summary":null,"start":129839593,"end":130017129,"strand":-1,"description":"family with sequence similarity 49 member B [Source:HGNC Symbol;Acc:HGNC:25216]"}, {"versioned_ensembl_gene_id":"ENSG00000157036.12","gene_symbol":"EXOG","gene_name":"exo/endonuclease G [Source:HGNC Symbol;Acc:HGNC:3347]","synonyms":"ENGL-b,ENGL-a,ENGL,ENDOGL2,ENDOGL1","biotype":"protein_coding","ncbi_id":"9941","summary":"This gene encodes an endo/exonuclease with 5'-3' exonuclease activity. The encoded enzyme catalyzes the hydrolysis of ester linkages at the 5' end of a nucleic acid chain. This enzyme is localized to the mitochondria and may play a role in programmed cell death. Alternatively spliced transcript variants have been described. A pseudogene exists on chromosome 18. [provided by RefSeq, Feb 2009]","start":38496127,"end":38542161,"strand":1,"description":"exo/endonuclease G [Source:HGNC Symbol;Acc:HGNC:3347]"}, {"versioned_ensembl_gene_id":"ENSG00000282697.1","gene_symbol":"AC073488.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9409748,"end":9410501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282222.1","gene_symbol":"AC073488.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9410789,"end":9411545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110944.8","gene_symbol":"IL23A","gene_name":"interleukin 23 subunit alpha [Source:HGNC Symbol;Acc:HGNC:15488]","synonyms":"IL-23A,IL-23,SGRF,P19,IL23P19","biotype":"protein_coding","ncbi_id":"51561","summary":"This gene encodes a subunit of the heterodimeric cytokine interleukin 23 (IL23). IL23 is composed of this protein and the p40 subunit of interleukin 12 (IL12B). The receptor of IL23 is formed by the beta 1 subunit of IL12 (IL12RB1) and an IL23 specific subunit, IL23R. Both IL23 and IL12 can activate the transcription activator STAT4, and stimulate the production of interferon-gamma (IFNG). In contrast to IL12, which acts mainly on naive CD4(+) T cells, IL23 preferentially acts on memory CD4(+) T cells. [provided by RefSeq, Jul 2008]","start":56334174,"end":56340410,"strand":1,"description":"interleukin 23 subunit alpha [Source:HGNC Symbol;Acc:HGNC:15488]"}, {"versioned_ensembl_gene_id":"ENSG00000281955.1","gene_symbol":"AC073488.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9411701,"end":9412478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281941.1","gene_symbol":"AC073488.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9412772,"end":9413522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183239.5","gene_symbol":"AL109615.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44089242,"end":44089696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169221.13","gene_symbol":"TBC1D10B","gene_name":"TBC1 domain family member 10B [Source:HGNC Symbol;Acc:HGNC:24510]","synonyms":"Rab27A-GAPbeta,FLJ13130,EPI64B,DKFZP434P1750","biotype":"protein_coding","ncbi_id":"26000","summary":"Small G proteins of the RAB family (see MIM 179508) function in intracellular vesicle trafficking by switching from the GTP-bound state to the GDP-bound state with the assistance of guanine nucleotide exchange factors (GEFs; see MIM 609700) and GTPase-activating proteins (GAPs). TBC1D10B functions as a GAP for several proteins of the Rab family (Ishibashi et al., 2009 [PubMed 19077034]).[supplied by OMIM, Nov 2010]","start":30357102,"end":30370264,"strand":-1,"description":"TBC1 domain family member 10B [Source:HGNC Symbol;Acc:HGNC:24510]"}, {"versioned_ensembl_gene_id":"ENSG00000262299.1","gene_symbol":"AL513523.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":153812404,"end":153819322,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251463.2","gene_symbol":"FKBP4P1","gene_name":"FK506 binding protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44038]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132656","summary":null,"start":118193405,"end":118194751,"strand":-1,"description":"FK506 binding protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44038]"}, {"versioned_ensembl_gene_id":"ENSG00000164100.8","gene_symbol":"NDST3","gene_name":"N-deacetylase and N-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:7682]","synonyms":"HSST3","biotype":"protein_coding","ncbi_id":"9348","summary":"This gene encodes a member of the heparan sulfate/heparin GlcNAc N-deacetylase/ N-sulfotransferase family. The encoded enzyme is a type II transmembrane protein that resides in the Golgi apparatus. This monomeric bifunctional enzyme catalyzes the N-deacetylation and N-sulfation of N-acetylglucosamine residues in heparan sulfate and heparin, which are the initial chemical modifications required for the biosynthesis of the functional oligosaccharide sequences that define the specific ligand binding activities of heparan sulfate and heparin. [provided by RefSeq, Nov 2008]","start":118033618,"end":118258648,"strand":1,"description":"N-deacetylase and N-sulfotransferase 3 [Source:HGNC Symbol;Acc:HGNC:7682]"}, {"versioned_ensembl_gene_id":"ENSG00000282300.1","gene_symbol":"AC073488.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9413816,"end":9414569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249493.1","gene_symbol":"ANKRD20A18P","gene_name":"ankyrin repeat domain 20 family member A18, pseudogene [Source:HGNC Symbol;Acc:HGNC:23756]","synonyms":"C21orf126","biotype":"unprocessed_pseudogene","ncbi_id":"391269","summary":null,"start":14064325,"end":14069087,"strand":1,"description":"ankyrin repeat domain 20 family member A18, pseudogene [Source:HGNC Symbol;Acc:HGNC:23756]"}, {"versioned_ensembl_gene_id":"ENSG00000215871.2","gene_symbol":"AC104457.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100331804,"end":100332617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230454.1","gene_symbol":"U73166.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50260303,"end":50263358,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223978.1","gene_symbol":"ZNF736P1Y","gene_name":"zinc finger protein 736 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:37726]","synonyms":"ZNF736P1","biotype":"processed_pseudogene","ncbi_id":"442486","summary":null,"start":24985201,"end":24986476,"strand":-1,"description":"zinc finger protein 736 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:37726]"}, {"versioned_ensembl_gene_id":"ENSG00000237380.6","gene_symbol":"HOXD-AS2","gene_name":"HOXD cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43756]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506783","summary":null,"start":176121611,"end":176137098,"strand":-1,"description":"HOXD cluster antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:43756]"}, {"versioned_ensembl_gene_id":"ENSG00000228056.3","gene_symbol":"CFL1P3","gene_name":"cofilin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1879]","synonyms":"CFLP3,CFLL3","biotype":"processed_pseudogene","ncbi_id":"100131874","summary":null,"start":63843196,"end":63843685,"strand":-1,"description":"cofilin 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1879]"}, {"versioned_ensembl_gene_id":"ENSG00000205809.9","gene_symbol":"KLRC2","gene_name":"killer cell lectin like receptor C2 [Source:HGNC Symbol;Acc:HGNC:6375]","synonyms":"NKG2-C,CD159c","biotype":"protein_coding","ncbi_id":"3822","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. The group, designated KLRC (NKG2) are expressed primarily in natural killer (NK) cells and encodes a family of transmembrane proteins characterized by a type II membrane orientation (extracellular C terminus) and the presence of a C-type lectin domain. The KLRC (NKG2) gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed on NK cells. KLRC2 alternative splice variants have been described but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":10426854,"end":10442300,"strand":-1,"description":"killer cell lectin like receptor C2 [Source:HGNC Symbol;Acc:HGNC:6375]"}, {"versioned_ensembl_gene_id":"ENSG00000243792.1","gene_symbol":"OR7E89P","gene_name":"olfactory receptor family 7 subfamily E member 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:14730]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79540","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158853755,"end":158854576,"strand":1,"description":"olfactory receptor family 7 subfamily E member 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:14730]"}, {"versioned_ensembl_gene_id":"ENSG00000215003.4","gene_symbol":"AC130651.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15931697,"end":15932294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206378.10","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31853571,"end":31869426,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000275725.1","gene_symbol":"AC104010.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44656771,"end":44656920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138079.13","gene_symbol":"SLC3A1","gene_name":"solute carrier family 3 member 1 [Source:HGNC Symbol;Acc:HGNC:11025]","synonyms":"ATR1,RBAT,NBAT,D2H,CSNU1","biotype":"protein_coding","ncbi_id":"6519","summary":"This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":44275458,"end":44321494,"strand":1,"description":"solute carrier family 3 member 1 [Source:HGNC Symbol;Acc:HGNC:11025]"}, {"versioned_ensembl_gene_id":"ENSG00000231869.1","gene_symbol":"AL844853.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31874140,"end":31874433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230075.1","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478955","summary":null,"start":31990371,"end":31993900,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000224518.2","gene_symbol":"AC006989.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14941746,"end":14942715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008130.15","gene_symbol":"NADK","gene_name":"NAD kinase [Source:HGNC Symbol;Acc:HGNC:29831]","synonyms":"FLJ13052","biotype":"protein_coding","ncbi_id":"65220","summary":"NADK catalyzes the transfer of a phosphate group from ATP to NAD to generate NADP, which in its reduced form acts as an electron donor for biosynthetic reactions (Lerner et al., 2001 [PubMed 11594753]).[supplied by OMIM, Mar 2008]","start":1751232,"end":1780457,"strand":-1,"description":"NAD kinase [Source:HGNC Symbol;Acc:HGNC:29831]"}, {"versioned_ensembl_gene_id":"ENSG00000178115.11","gene_symbol":"GOLGA8Q","gene_name":"golgin A8 family member Q [Source:HGNC Symbol;Acc:HGNC:44408]","synonyms":null,"biotype":"protein_coding","ncbi_id":"727909","summary":null,"start":30552078,"end":30562501,"strand":1,"description":"golgin A8 family member Q [Source:HGNC Symbol;Acc:HGNC:44408]"}, {"versioned_ensembl_gene_id":"ENSG00000100288.19","gene_symbol":"CHKB","gene_name":"choline kinase beta [Source:HGNC Symbol;Acc:HGNC:1938]","synonyms":"CHKL,CHETK","biotype":"protein_coding","ncbi_id":"1120","summary":"Choline kinase (CK) and ethanolamine kinase (EK) catalyze the phosphorylation of choline/ethanolamine to phosphocholine/phosphoethanolamine. This is the first enzyme in the biosynthesis of phosphatidylcholine/phosphatidylethanolamine in all animal cells. The highly purified CKs from mammalian sources and their recombinant gene products have been shown to have EK activity also, indicating that both activities reside on the same protein. The choline kinase-like protein encoded by CHKL belongs to the choline/ethanolamine kinase family; however, its exact function is not known. Read-through transcripts are expressed from this locus that include exons from the downstream CPT1B locus. [provided by RefSeq, Jun 2009]","start":50578949,"end":50601455,"strand":-1,"description":"choline kinase beta [Source:HGNC Symbol;Acc:HGNC:1938]"}, {"versioned_ensembl_gene_id":"ENSG00000236960.1","gene_symbol":"AL354695.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19491072,"end":19491299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226255.1","gene_symbol":"UBE2V2P1","gene_name":"ubiquitin conjugating enzyme E2 V2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44885]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128493","summary":null,"start":19051455,"end":19052170,"strand":1,"description":"ubiquitin conjugating enzyme E2 V2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44885]"}, {"versioned_ensembl_gene_id":"ENSG00000227734.1","gene_symbol":"AL590378.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19290223,"end":19291480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248448.2","gene_symbol":"COX5BP1","gene_name":"cytochrome c oxidase subunit 5B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2270]","synonyms":"COX5BL1","biotype":"processed_pseudogene","ncbi_id":"1330","summary":null,"start":81919995,"end":81920387,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2270]"}, {"versioned_ensembl_gene_id":"ENSG00000260447.1","gene_symbol":"AC009065.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2119207,"end":2120248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261123.1","gene_symbol":"AC009065.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2094830,"end":2097026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150873.11","gene_symbol":"C2orf50","gene_name":"chromosome 2 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:26324]","synonyms":"FLJ25143","biotype":"protein_coding","ncbi_id":"130813","summary":null,"start":11133053,"end":11146790,"strand":1,"description":"chromosome 2 open reading frame 50 [Source:HGNC Symbol;Acc:HGNC:26324]"}, {"versioned_ensembl_gene_id":"ENSG00000159403.15","gene_symbol":"C1R","gene_name":"complement C1r [Source:HGNC Symbol;Acc:HGNC:1246]","synonyms":null,"biotype":"protein_coding","ncbi_id":"715","summary":"This gene encodes a member of the peptidase S1 protein family. The encoded protein is a proteolytic subunit in the complement system C1 complex. The complement system acts as a mediator in the innate immune response by ultimately triggering phagocytosis, inflammation, and rupturing the bacterial cell wall. Mutations in this gene are associated with Ehlers-Danlos Syndrome. [provided by RefSeq, Dec 2018]","start":7080209,"end":7092607,"strand":-1,"description":"complement C1r [Source:HGNC Symbol;Acc:HGNC:1246]"}, {"versioned_ensembl_gene_id":"ENSG00000223884.5","gene_symbol":"AC068481.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7062727,"end":7077880,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280312.1","gene_symbol":"Z83836.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47259366,"end":47261007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223636.1","gene_symbol":"UBE2Q2P5Y","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38466]","synonyms":"UBE2Q2PY2","biotype":"unprocessed_pseudogene","ncbi_id":"100421717","summary":null,"start":25431156,"end":25437315,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 5, Y-linked [Source:HGNC Symbol;Acc:HGNC:38466]"}, {"versioned_ensembl_gene_id":"ENSG00000281569.1","gene_symbol":"KANSL1-AS1","gene_name":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644246","summary":null,"start":45899740,"end":45902887,"strand":-1,"description":"KANSL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43740]"}, {"versioned_ensembl_gene_id":"ENSG00000254152.1","gene_symbol":"AC109329.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30349866,"end":30350347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092068.19","gene_symbol":"SLC7A8","gene_name":"solute carrier family 7 member 8 [Source:HGNC Symbol;Acc:HGNC:11066]","synonyms":"LPI-PC1,LAT2","biotype":"protein_coding","ncbi_id":"23428","summary":null,"start":23125295,"end":23183674,"strand":-1,"description":"solute carrier family 7 member 8 [Source:HGNC Symbol;Acc:HGNC:11066]"}, {"versioned_ensembl_gene_id":"ENSG00000270488.1","gene_symbol":"AC079587.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10874291,"end":10874567,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277720.1","gene_symbol":"AL031777.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26219045,"end":26219240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143621.16","gene_symbol":"ILF2","gene_name":"interleukin enhancer binding factor 2 [Source:HGNC Symbol;Acc:HGNC:6037]","synonyms":"NF45","biotype":"protein_coding","ncbi_id":"3608","summary":"The protein encoded by this gene is a transcription factor required for T-cell expression of the interleukin 2 gene. It also binds RNA and is an essential component for encapsidation and protein priming of hepatitis B viral polymerase. The encoded 45 kDa protein (NF45, ILF2) forms a complex with the 90 kDa interleukin enhancer-binding factor 3 (NF90, ILF3), and this complex has been shown to affect the redistribution of nuclear mRNA to the cytoplasm, to repair DNA breaks by nonhomologous end joining, and to negatively regulate the microRNA processing pathway. Knockdown of NF45 or NF90 protein retards cell growth, possibly by inhibition of mRNA stabilization. Alternative splicing results in multiple transcript variants. Related pseudogenes have been found on chromosomes 3 and 14. [provided by RefSeq, Dec 2014]","start":153661788,"end":153671048,"strand":-1,"description":"interleukin enhancer binding factor 2 [Source:HGNC Symbol;Acc:HGNC:6037]"}, {"versioned_ensembl_gene_id":"ENSG00000179178.10","gene_symbol":"TMEM125","gene_name":"transmembrane protein 125 [Source:HGNC Symbol;Acc:HGNC:28275]","synonyms":"MGC17299","biotype":"protein_coding","ncbi_id":"128218","summary":null,"start":43269994,"end":43274002,"strand":1,"description":"transmembrane protein 125 [Source:HGNC Symbol;Acc:HGNC:28275]"}, {"versioned_ensembl_gene_id":"ENSG00000271991.1","gene_symbol":"AC013400.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19902025,"end":19902569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228701.1","gene_symbol":"TNKS2-AS1","gene_name":"TNKS2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45173]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507633","summary":null,"start":91782839,"end":91798291,"strand":-1,"description":"TNKS2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45173]"}, {"versioned_ensembl_gene_id":"ENSG00000159110.19","gene_symbol":"IFNAR2","gene_name":"interferon alpha and beta receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:5433]","synonyms":"IFNABR","biotype":"protein_coding","ncbi_id":"3455","summary":"The protein encoded by this gene is a type I membrane protein that forms one of the two chains of a receptor for interferons alpha and beta. Binding and activation of the receptor stimulates Janus protein kinases, which in turn phosphorylate several proteins, including STAT1 and STAT2. The protein belongs to the type II cytokine receptor family. Mutations in this gene are associated with Immunodeficiency 45. [provided by RefSeq, Jul 2020]","start":33229901,"end":33265675,"strand":1,"description":"interferon alpha and beta receptor subunit 2 [Source:HGNC Symbol;Acc:HGNC:5433]"}, {"versioned_ensembl_gene_id":"ENSG00000158850.14","gene_symbol":"B4GALT3","gene_name":"beta-1,4-galactosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:926]","synonyms":"beta4Gal-T3","biotype":"protein_coding","ncbi_id":"8703","summary":"This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: GlcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and which then remains uncleaved to function as a transmembrane anchor. By sequence similarity, the beta4GalTs form four groups: beta4GalT1 and beta4GalT2, beta4GalT3 and beta4GalT4, beta4GalT5 and beta4GalT6, and beta4GalT7. This gene encodes an enzyme that may be mainly involved in the synthesis of the first N-acetyllactosamine unit of poly-N-acetyllactosamine chains. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":161171310,"end":161177968,"strand":-1,"description":"beta-1,4-galactosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:926]"}, {"versioned_ensembl_gene_id":"ENSG00000067082.14","gene_symbol":"KLF6","gene_name":"Kruppel like factor 6 [Source:HGNC Symbol;Acc:HGNC:2235]","synonyms":"Zf9,ST12,PAC1,GBF,CPBP,COPEB,BCD1","biotype":"protein_coding","ncbi_id":"1316","summary":"This gene encodes a member of the Kruppel-like family of transcription factors. The zinc finger protein is a transcriptional activator, and functions as a tumor suppressor. Multiple transcript variants encoding different isoforms have been found for this gene, some of which are implicated in carcinogenesis. [provided by RefSeq, May 2009]","start":3775996,"end":3785281,"strand":-1,"description":"Kruppel like factor 6 [Source:HGNC Symbol;Acc:HGNC:2235]"}, {"versioned_ensembl_gene_id":"ENSG00000232312.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"D6S54E,GPATCH10,BAT4,G5,ANKRD59","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31737508,"end":31742562,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000231939.5","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"HLA-DQB,CELIAC1,IDDM1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32748163,"end":32755410,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000242214.1","gene_symbol":"MTND3P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42146]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873182","summary":null,"start":106896483,"end":106896821,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42146]"}, {"versioned_ensembl_gene_id":"ENSG00000243918.1","gene_symbol":"EIF4BP8","gene_name":"eukaryotic translation initiation factor 4B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37941]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339881","summary":null,"start":122660613,"end":122662438,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37941]"}, {"versioned_ensembl_gene_id":"ENSG00000143207.19","gene_symbol":"RFWD2","gene_name":"ring finger and WD repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:17440]","synonyms":"RNF200,FLJ10416,COP1","biotype":"protein_coding","ncbi_id":"64326","summary":null,"start":175944831,"end":176207493,"strand":-1,"description":"ring finger and WD repeat domain 2 [Source:HGNC Symbol;Acc:HGNC:17440]"}, {"versioned_ensembl_gene_id":"ENSG00000224711.1","gene_symbol":"LINC01706","gene_name":"long intergenic non-protein coding RNA 1706 [Source:HGNC Symbol;Acc:HGNC:52494]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929312","summary":null,"start":7347467,"end":7367632,"strand":1,"description":"long intergenic non-protein coding RNA 1706 [Source:HGNC Symbol;Acc:HGNC:52494]"}, {"versioned_ensembl_gene_id":"ENSG00000277424.4","gene_symbol":"HMOX2","gene_name":"heme oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:5014]","synonyms":"HO-2","biotype":"protein_coding","ncbi_id":"3163","summary":"Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. Several alternatively spliced transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]","start":4476649,"end":4512306,"strand":1,"description":"heme oxygenase 2 [Source:HGNC Symbol;Acc:HGNC:5014]"}, {"versioned_ensembl_gene_id":"ENSG00000242052.1","gene_symbol":"RPL10P7","gene_name":"ribosomal protein L10 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442086","summary":null,"start":119635526,"end":119636150,"strand":-1,"description":"ribosomal protein L10 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35974]"}, {"versioned_ensembl_gene_id":"ENSG00000188290.10","gene_symbol":"HES4","gene_name":"hes family bHLH transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:24149]","synonyms":"bHLHb42","biotype":"protein_coding","ncbi_id":"57801","summary":null,"start":998962,"end":1000172,"strand":-1,"description":"hes family bHLH transcription factor 4 [Source:HGNC Symbol;Acc:HGNC:24149]"}, {"versioned_ensembl_gene_id":"ENSG00000099783.11","gene_symbol":"HNRNPM","gene_name":"heterogeneous nuclear ribonucleoprotein M [Source:HGNC Symbol;Acc:HGNC:5046]","synonyms":"NAGR1,HTGR1,HNRPM4,HNRPM,HNRNPM4,CEAR","biotype":"protein_coding","ncbi_id":"4670","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNAs. This protein also constitutes a monomer of the N-acetylglucosamine-specific receptor which is postulated to trigger selective recycling of immature GlcNAc-bearing thyroglobulin molecules. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":8444767,"end":8489114,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein M [Source:HGNC Symbol;Acc:HGNC:5046]"}, {"versioned_ensembl_gene_id":"ENSG00000229057.1","gene_symbol":"RPS3AP54","gene_name":"ribosomal protein S3a pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:49750]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927101","summary":null,"start":6662424,"end":6663792,"strand":1,"description":"ribosomal protein S3a pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:49750]"}, {"versioned_ensembl_gene_id":"ENSG00000262503.1","gene_symbol":"AC027763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6927472,"end":6928191,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148541.12","gene_symbol":"FAM13C","gene_name":"family with sequence similarity 13 member C [Source:HGNC Symbol;Acc:HGNC:19371]","synonyms":"FAM13C1","biotype":"protein_coding","ncbi_id":"220965","summary":null,"start":59246129,"end":59363181,"strand":-1,"description":"family with sequence similarity 13 member C [Source:HGNC Symbol;Acc:HGNC:19371]"}, {"versioned_ensembl_gene_id":"ENSG00000254303.1","gene_symbol":"AC037486.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121954640,"end":122127184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131089.15","gene_symbol":"ARHGEF9","gene_name":"Cdc42 guanine nucleotide exchange factor 9 [Source:HGNC Symbol;Acc:HGNC:14561]","synonyms":"PEM-2,KIAA0424","biotype":"protein_coding","ncbi_id":"23229","summary":"The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. This brain-specific protein also acts as an adaptor protein for the recruitment of gephyrin and together these proteins facilitate receceptor recruitement in GABAnergic and glycinergic synapses. Defects in this gene are the cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy, as well as several other types of cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":63634967,"end":63809274,"strand":-1,"description":"Cdc42 guanine nucleotide exchange factor 9 [Source:HGNC Symbol;Acc:HGNC:14561]"}, {"versioned_ensembl_gene_id":"ENSG00000167657.13","gene_symbol":"DAPK3","gene_name":"death associated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:2676]","synonyms":"ZIPK,ZIP","biotype":"protein_coding","ncbi_id":"1613","summary":"Death-associated protein kinase 3 (DAPK3) induces morphological changes in apoptosis when overexpressed in mammalian cells. These results suggest that DAPK3 may play a role in the induction of apoptosis. [provided by RefSeq, Jul 2008]","start":3958453,"end":3971123,"strand":-1,"description":"death associated protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:2676]"}, {"versioned_ensembl_gene_id":"ENSG00000236813.1","gene_symbol":"BTF3P8","gene_name":"basic transcription factor 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38572]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652961","summary":null,"start":63766875,"end":63767400,"strand":1,"description":"basic transcription factor 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38572]"}, {"versioned_ensembl_gene_id":"ENSG00000163762.6","gene_symbol":"TM4SF18","gene_name":"transmembrane 4 L six family member 18 [Source:HGNC Symbol;Acc:HGNC:25181]","synonyms":"L6D","biotype":"protein_coding","ncbi_id":"116441","summary":null,"start":149318498,"end":149334414,"strand":-1,"description":"transmembrane 4 L six family member 18 [Source:HGNC Symbol;Acc:HGNC:25181]"}, {"versioned_ensembl_gene_id":"ENSG00000226222.3","gene_symbol":"AC079168.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24632257,"end":24632601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158055.15","gene_symbol":"GRHL3","gene_name":"grainyhead like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:25839]","synonyms":"TFCP2L4,SOM","biotype":"protein_coding","ncbi_id":"57822","summary":"This gene encodes a member of the grainyhead family of transcription factors. The encoded protein may function as a transcription factor during development, and has been shown to stimulate migration of endothelial cells. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Aug 2010]","start":24319322,"end":24364482,"strand":1,"description":"grainyhead like transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:25839]"}, {"versioned_ensembl_gene_id":"ENSG00000226767.1","gene_symbol":"AC114501.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65508773,"end":65508944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257677.1","gene_symbol":"LINC02464","gene_name":"long intergenic non-protein coding RNA 2464 [Source:HGNC Symbol;Acc:HGNC:53401]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369854","summary":null,"start":77219603,"end":77228693,"strand":-1,"description":"long intergenic non-protein coding RNA 2464 [Source:HGNC Symbol;Acc:HGNC:53401]"}, {"versioned_ensembl_gene_id":"ENSG00000234390.4","gene_symbol":"USP27X-AS1","gene_name":"USP27X antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27249]","synonyms":null,"biotype":"lincRNA","ncbi_id":"158572","summary":null,"start":49876724,"end":49879241,"strand":-1,"description":"USP27X antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27249]"}, {"versioned_ensembl_gene_id":"ENSG00000242828.1","gene_symbol":"AC068756.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80761042,"end":80788963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214022.11","gene_symbol":"REPIN1","gene_name":"replication initiator 1 [Source:HGNC Symbol;Acc:HGNC:17922]","synonyms":"ZNF464,Zfp464,RIP60,H_DJ0584D14.12,AP4","biotype":"protein_coding","ncbi_id":"29803","summary":null,"start":150368189,"end":150374044,"strand":1,"description":"replication initiator 1 [Source:HGNC Symbol;Acc:HGNC:17922]"}, {"versioned_ensembl_gene_id":"ENSG00000261444.1","gene_symbol":"AC106782.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30214409,"end":30214699,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135535.15","gene_symbol":"CD164","gene_name":"CD164 molecule [Source:HGNC Symbol;Acc:HGNC:1632]","synonyms":"MUC-24,MGC-24,DFNA66","biotype":"protein_coding","ncbi_id":"8763","summary":"This gene encodes a transmembrane sialomucin and cell adhesion molecule that regulates the proliferation, adhesion and migration of hematopoietic progenitor cells. The encoded protein also interacts with the C-X-C chemokine receptor type 4 and may regulate muscle development. Elevated expression of this gene has been observed in human patients with Sezary syndrome, a type of blood cancer, and a mutation in this gene may be associated with impaired hearing. [provided by RefSeq, Oct 2016]","start":109366514,"end":109382457,"strand":-1,"description":"CD164 molecule [Source:HGNC Symbol;Acc:HGNC:1632]"}, {"versioned_ensembl_gene_id":"ENSG00000228799.5","gene_symbol":"LINC01939","gene_name":"long intergenic non-protein coding RNA 1939 [Source:HGNC Symbol;Acc:HGNC:52762]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101060385","summary":null,"start":900216,"end":905451,"strand":-1,"description":"long intergenic non-protein coding RNA 1939 [Source:HGNC Symbol;Acc:HGNC:52762]"}, {"versioned_ensembl_gene_id":"ENSG00000237446.1","gene_symbol":"RHEBP3","gene_name":"Ras-homolog enriched in brain pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44992]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"692231","summary":null,"start":18019214,"end":18020200,"strand":1,"description":"Ras-homolog enriched in brain pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44992]"}, {"versioned_ensembl_gene_id":"ENSG00000278585.1","gene_symbol":"SNX3P1Y","gene_name":"sorting nexin 3 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:41517]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873885","summary":null,"start":5634480,"end":5634655,"strand":-1,"description":"sorting nexin 3 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:41517]"}, {"versioned_ensembl_gene_id":"ENSG00000100429.17","gene_symbol":"HDAC10","gene_name":"histone deacetylase 10 [Source:HGNC Symbol;Acc:HGNC:18128]","synonyms":"DKFZP761B039","biotype":"protein_coding","ncbi_id":"83933","summary":"The protein encoded by this gene belongs to the histone deacetylase family, members of which deacetylate lysine residues on the N-terminal part of the core histones. Histone deacetylation modulates chromatin structure, and plays an important role in transcriptional regulation, cell cycle progression, and developmental events. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":50245183,"end":50251405,"strand":-1,"description":"histone deacetylase 10 [Source:HGNC Symbol;Acc:HGNC:18128]"}, {"versioned_ensembl_gene_id":"ENSG00000237910.1","gene_symbol":"MTCO1P18","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52020]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075143","summary":null,"start":131382643,"end":131384061,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52020]"}, {"versioned_ensembl_gene_id":"ENSG00000105643.9","gene_symbol":"ARRDC2","gene_name":"arrestin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25225]","synonyms":"PP2703,CLONE24945","biotype":"protein_coding","ncbi_id":"27106","summary":null,"start":18001132,"end":18014102,"strand":1,"description":"arrestin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25225]"}, {"versioned_ensembl_gene_id":"ENSG00000255866.1","gene_symbol":"AC090023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65559591,"end":65560889,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279172.1","gene_symbol":"AC020904.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18009440,"end":18009881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106538.9","gene_symbol":"RARRES2","gene_name":"retinoic acid receptor responder 2 [Source:HGNC Symbol;Acc:HGNC:9868]","synonyms":"TIG2,HP10433","biotype":"protein_coding","ncbi_id":"5919","summary":"This gene encodes a secreted chemotactic protein that initiates chemotaxis via the ChemR23 G protein-coupled seven-transmembrane domain ligand. Expression of this gene is upregulated by the synthetic retinoid tazarotene and occurs in a wide variety of tissues. The active protein has several roles, including that as an adipokine and as an antimicrobial protein with activity against bacteria and fungi. [provided by RefSeq, Nov 2014]","start":150338317,"end":150341674,"strand":-1,"description":"retinoic acid receptor responder 2 [Source:HGNC Symbol;Acc:HGNC:9868]"}, {"versioned_ensembl_gene_id":"ENSG00000228478.1","gene_symbol":"AL138885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10423140,"end":10426176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111674.8","gene_symbol":"ENO2","gene_name":"enolase 2 [Source:HGNC Symbol;Acc:HGNC:3353]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2026","summary":"This gene encodes one of the three enolase isoenzymes found in mammals. This isoenzyme, a homodimer, is found in mature neurons and cells of neuronal origin. A switch from alpha enolase to gamma enolase occurs in neural tissue during development in rats and primates. [provided by RefSeq, Jul 2008]","start":6913745,"end":6923698,"strand":1,"description":"enolase 2 [Source:HGNC Symbol;Acc:HGNC:3353]"}, {"versioned_ensembl_gene_id":"ENSG00000260257.2","gene_symbol":"AL035071.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32856621,"end":32858751,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231802.1","gene_symbol":"AC009502.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":219684030,"end":219684795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267919.1","gene_symbol":"AC009955.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219645090,"end":219645631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008128.22","gene_symbol":"CDK11A","gene_name":"cyclin dependent kinase 11A [Source:HGNC Symbol;Acc:HGNC:1730]","synonyms":"PITSLRE,p58GTA,CDK11-p58,CDK11-p46,CDK11-p110,CDC2L3,CDC2L2","biotype":"protein_coding","ncbi_id":"728642","summary":"This gene encodes a member of the serine/threonine protein kinase family. Members of this kinase family are known to be essential for eukaryotic cell cycle control. Due to a segmental duplication, this gene shares very high sequence identity with a neighboring gene. These two genes are frequently deleted or altered in neuroblastoma. The protein kinase encoded by this gene can be cleaved by caspases and may play a role in cell apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":1702730,"end":1724324,"strand":-1,"description":"cyclin dependent kinase 11A [Source:HGNC Symbol;Acc:HGNC:1730]"}, {"versioned_ensembl_gene_id":"ENSG00000267390.1","gene_symbol":"AC036176.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63367328,"end":63381629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235112.1","gene_symbol":"HSPE1P27","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:49346]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480261","summary":null,"start":21161475,"end":21162081,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:49346]"}, {"versioned_ensembl_gene_id":"ENSG00000233487.6","gene_symbol":"RPSAP69","gene_name":"ribosomal protein SA pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:51922]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"101927158","summary":null,"start":196983890,"end":196987558,"strand":-1,"description":"ribosomal protein SA pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:51922]"}, {"versioned_ensembl_gene_id":"ENSG00000270669.1","gene_symbol":"AC008638.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77216416,"end":77216878,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262587.2","gene_symbol":"AC133552.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25031744,"end":25058109,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260714.1","gene_symbol":"AC133552.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25015978,"end":25021023,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119227.7","gene_symbol":"PIGZ","gene_name":"phosphatidylinositol glycan anchor biosynthesis class Z [Source:HGNC Symbol;Acc:HGNC:30596]","synonyms":"FLJ12768,SMP3,MGC52163","biotype":"protein_coding","ncbi_id":"80235","summary":"The glycosylphosphatidylinositol (GPI) anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface. This gene encodes a protein that is localized to the endoplasmic reticulum, and is involved in GPI anchor biosynthesis. As shown for the yeast homolog, which is a member of a family of dolichol-phosphate-mannose (Dol-P-Man)-dependent mannosyltransferases, this protein can also add a side-branching fourth mannose to GPI precursors during the assembly of GPI anchors. [provided by RefSeq, Jul 2008]","start":196946343,"end":196969060,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class Z [Source:HGNC Symbol;Acc:HGNC:30596]"}, {"versioned_ensembl_gene_id":"ENSG00000137558.7","gene_symbol":"PI15","gene_name":"peptidase inhibitor 15 [Source:HGNC Symbol;Acc:HGNC:8946]","synonyms":"P25TI","biotype":"protein_coding","ncbi_id":"51050","summary":"This gene encodes a trypsin inhibitor. The protein shares similarity to insect venom allergens, mammalian testis-specific proteins and plant pathogenesis-related proteins. It is frequently expressed in human neuroblastoma and glioblastoma cell lines, and thus may play a role in the central nervous system. [provided by RefSeq, Jul 2008]","start":74824537,"end":74855029,"strand":1,"description":"peptidase inhibitor 15 [Source:HGNC Symbol;Acc:HGNC:8946]"}, {"versioned_ensembl_gene_id":"ENSG00000272813.1","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107765,"end":42108953,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000232042.1","gene_symbol":"AL512286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":120273127,"end":120273526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091127.13","gene_symbol":"PUS7","gene_name":"pseudouridylate synthase 7 (putative) [Source:HGNC Symbol;Acc:HGNC:26033]","synonyms":"FLJ20485","biotype":"protein_coding","ncbi_id":"54517","summary":null,"start":105439661,"end":105522267,"strand":-1,"description":"pseudouridylate synthase 7 (putative) [Source:HGNC Symbol;Acc:HGNC:26033]"}, {"versioned_ensembl_gene_id":"ENSG00000245694.9","gene_symbol":"CRNDE","gene_name":"colorectal neoplasia differentially expressed [Source:HGNC Symbol;Acc:HGNC:37078]","synonyms":"LOC643911,LINC00180,CRNDEP","biotype":"lincRNA","ncbi_id":"643911","summary":"This gene is transcribed into multiple transcript variants, some of which may function as non-coding RNAs. One of the transcript variants encodes a putative short protein that is localized to the nucleus (PMID:25978564). Expression of this locus is increased in proliferating tissues, including certain tumors such as colorectal adenomas and adenocarcinomas. Transcription from this gene is negatively regulated by insulin and insulin-like growth factors, and may regulate the expression of genes involved in metabolism. [provided by RefSeq, May 2015]","start":54845189,"end":54929189,"strand":-1,"description":"colorectal neoplasia differentially expressed [Source:HGNC Symbol;Acc:HGNC:37078]"}, {"versioned_ensembl_gene_id":"ENSG00000251511.1","gene_symbol":"AC096736.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156585979,"end":156590039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248730.1","gene_symbol":"EGFLAM-AS4","gene_name":"EGFLAM antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:41166]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100852408","summary":null,"start":38282264,"end":38290986,"strand":-1,"description":"EGFLAM antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:41166]"}, {"versioned_ensembl_gene_id":"ENSG00000251257.2","gene_symbol":"AC010457.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38460925,"end":38468339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255582.1","gene_symbol":"OR10G2","gene_name":"olfactory receptor family 10 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8170]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26534","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21633836,"end":21634940,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 2 [Source:HGNC Symbol;Acc:HGNC:8170]"}, {"versioned_ensembl_gene_id":"ENSG00000233272.1","gene_symbol":"PNPT1P2","gene_name":"polyribonucleotide nucleotidyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44469]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533721","summary":null,"start":121842368,"end":121845131,"strand":-1,"description":"polyribonucleotide nucleotidyltransferase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44469]"}, {"versioned_ensembl_gene_id":"ENSG00000244509.3","gene_symbol":"APOBEC3C","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3C [Source:HGNC Symbol;Acc:HGNC:17353]","synonyms":"PBI,bK150C2.3,ARP5,ARDC4,ARDC2,APOBEC1L","biotype":"protein_coding","ncbi_id":"27350","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. [provided by RefSeq, Jul 2008]","start":39014083,"end":39020352,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3C [Source:HGNC Symbol;Acc:HGNC:17353]"}, {"versioned_ensembl_gene_id":"ENSG00000280973.1","gene_symbol":"AP000457.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17299421,"end":17299798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125726.10","gene_symbol":"CD70","gene_name":"CD70 molecule [Source:HGNC Symbol;Acc:HGNC:11937]","synonyms":"TNFSF7,CD27LG,CD27L","biotype":"protein_coding","ncbi_id":"970","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for TNFRSF27/CD27. It is a surface antigen on activated, but not on resting, T and B lymphocytes. It induces proliferation of costimulated T cells, enhances the generation of cytolytic T cells, and contributes to T cell activation. This cytokine is also reported to play a role in regulating B-cell activation, cytotoxic function of natural killer cells, and immunoglobulin sythesis. [provided by RefSeq, Jul 2008]","start":6583183,"end":6604103,"strand":-1,"description":"CD70 molecule [Source:HGNC Symbol;Acc:HGNC:11937]"}, {"versioned_ensembl_gene_id":"ENSG00000283448.1","gene_symbol":"GPR1","gene_name":"G protein-coupled receptor 1 [Source:HGNC Symbol;Acc:HGNC:4463]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2825","summary":null,"start":206175316,"end":206218047,"strand":-1,"description":"G protein-coupled receptor 1 [Source:HGNC Symbol;Acc:HGNC:4463]"}, {"versioned_ensembl_gene_id":"ENSG00000128383.12","gene_symbol":"APOBEC3A","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A [Source:HGNC Symbol;Acc:HGNC:17343]","synonyms":"PHRBN,ARP3","biotype":"protein_coding","ncbi_id":"200315","summary":"This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. The protein encoded by this gene lacks the zinc binding activity of other family members. The protein plays a role in immunity, by restricting transmission of foreign DNA such as viruses. One mechanism of foreign DNA restriction is deamination of foreign double-stranded DNA cytidines to uridines, which leads to DNA degradation. However, other mechanisms are also thought to be involved, as anti-viral effect is not dependent on deaminase activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]","start":38952741,"end":38992778,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A [Source:HGNC Symbol;Acc:HGNC:17343]"}, {"versioned_ensembl_gene_id":"ENSG00000164976.8","gene_symbol":"KIAA1161","gene_name":"KIAA1161 [Source:HGNC Symbol;Acc:HGNC:19918]","synonyms":"NET37","biotype":"protein_coding","ncbi_id":"57462","summary":null,"start":34366670,"end":34376853,"strand":-1,"description":"KIAA1161 [Source:HGNC Symbol;Acc:HGNC:19918]"}, {"versioned_ensembl_gene_id":"ENSG00000232090.2","gene_symbol":"AC016724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112995517,"end":112995937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256394.2","gene_symbol":"ASIC5","gene_name":"acid sensing ion channel subunit family member 5 [Source:HGNC Symbol;Acc:HGNC:17537]","synonyms":"INAC,HINAC,ACCN5,INAC,HINAC,ACCN5","biotype":"protein_coding","ncbi_id":"51802","summary":"This gene belongs to the amiloride-sensitive Na+ channel and degenerin (NaC/DEG) family, members of which have been identified in many animal species ranging from the nematode to human. The amiloride-sensitive Na(+) channel encoded by this gene is primarily expressed in the small intestine, however, its exact function is not known. [provided by RefSeq, Jul 2008]","start":155829729,"end":155866273,"strand":-1,"description":"acid sensing ion channel subunit family member 5 [Source:HGNC Symbol;Acc:HGNC:17537]"}, {"versioned_ensembl_gene_id":"ENSG00000235559.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"NOL5B,NOP56-L,dJ207F6.1,NOL5BP","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28783633,"end":28784004,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000236172.6","gene_symbol":"MIR7515HG","gene_name":"MIR7515 host gene [Source:HGNC Symbol;Acc:HGNC:49838]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102800314","summary":null,"start":6615389,"end":6650535,"strand":-1,"description":"MIR7515 host gene [Source:HGNC Symbol;Acc:HGNC:49838]"}, {"versioned_ensembl_gene_id":"ENSG00000116717.11","gene_symbol":"GADD45A","gene_name":"growth arrest and DNA damage inducible alpha [Source:HGNC Symbol;Acc:HGNC:4095]","synonyms":"GADD45,DDIT1","biotype":"protein_coding","ncbi_id":"1647","summary":"This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The protein encoded by this gene responds to environmental stresses by mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The DNA damage-induced transcription of this gene is mediated by both p53-dependent and -independent mechanisms. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[provided by RefSeq, Dec 2010]","start":67685061,"end":67688338,"strand":1,"description":"growth arrest and DNA damage inducible alpha [Source:HGNC Symbol;Acc:HGNC:4095]"}, {"versioned_ensembl_gene_id":"ENSG00000205929.10","gene_symbol":"C21orf62","gene_name":"chromosome 21 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:1305]","synonyms":"C21orf120,B37,PRED81","biotype":"protein_coding","ncbi_id":"56245","summary":null,"start":32793564,"end":32813743,"strand":-1,"description":"chromosome 21 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:1305]"}, {"versioned_ensembl_gene_id":"ENSG00000164893.8","gene_symbol":"SLC7A13","gene_name":"solute carrier family 7 member 13 [Source:HGNC Symbol;Acc:HGNC:23092]","synonyms":"XAT2,AGT-1","biotype":"protein_coding","ncbi_id":"157724","summary":null,"start":86214052,"end":86321146,"strand":-1,"description":"solute carrier family 7 member 13 [Source:HGNC Symbol;Acc:HGNC:23092]"}, {"versioned_ensembl_gene_id":"ENSG00000277755.1","gene_symbol":"AC138649.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22756172,"end":22756729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181817.5","gene_symbol":"LSM10","gene_name":"LSM10, U7 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:17562]","synonyms":"MGC15749","biotype":"protein_coding","ncbi_id":"84967","summary":null,"start":36391238,"end":36397892,"strand":-1,"description":"LSM10, U7 small nuclear RNA associated [Source:HGNC Symbol;Acc:HGNC:17562]"}, {"versioned_ensembl_gene_id":"ENSG00000271850.1","gene_symbol":"LINC02343","gene_name":"long intergenic non-protein coding RNA 2343 [Source:HGNC Symbol;Acc:HGNC:53263]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370158","summary":null,"start":34348043,"end":34614170,"strand":1,"description":"long intergenic non-protein coding RNA 2343 [Source:HGNC Symbol;Acc:HGNC:53263]"}, {"versioned_ensembl_gene_id":"ENSG00000206105.2","gene_symbol":"KRTAP20-4","gene_name":"keratin associated protein 20-4 [Source:HGNC Symbol;Acc:HGNC:34002]","synonyms":"KAP20.4","biotype":"protein_coding","ncbi_id":"100151643","summary":null,"start":30620627,"end":30620850,"strand":1,"description":"keratin associated protein 20-4 [Source:HGNC Symbol;Acc:HGNC:34002]"}, {"versioned_ensembl_gene_id":"ENSG00000277554.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2a,nkat2b,p58,CD158B2,cl-6,nkat2","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738470,"end":54752993,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000186925.6","gene_symbol":"KRTAP19-6","gene_name":"keratin associated protein 19-6 [Source:HGNC Symbol;Acc:HGNC:18941]","synonyms":"KAP19.6","biotype":"protein_coding","ncbi_id":"337973","summary":null,"start":30541535,"end":30541864,"strand":-1,"description":"keratin associated protein 19-6 [Source:HGNC Symbol;Acc:HGNC:18941]"}, {"versioned_ensembl_gene_id":"ENSG00000248265.1","gene_symbol":"FLJ12825","gene_name":"uncharacterized LOC440101 [Source:NCBI gene;Acc:440101]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440101","summary":null,"start":54058254,"end":54122234,"strand":1,"description":"uncharacterized LOC440101 [Source:NCBI gene;Acc:440101]"}, {"versioned_ensembl_gene_id":"ENSG00000239200.1","gene_symbol":"CR383656.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18692032,"end":18692408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257558.2","gene_symbol":"CR383656.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18667249,"end":18667370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275367.1","gene_symbol":"AC092111.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8217758,"end":8221115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162664.16","gene_symbol":"ZNF326","gene_name":"zinc finger protein 326 [Source:HGNC Symbol;Acc:HGNC:14104]","synonyms":"ZIRD,Zfp326,ZAN75,FLJ20403","biotype":"protein_coding","ncbi_id":"284695","summary":null,"start":89995112,"end":90035531,"strand":1,"description":"zinc finger protein 326 [Source:HGNC Symbol;Acc:HGNC:14104]"}, {"versioned_ensembl_gene_id":"ENSG00000275325.4","gene_symbol":"PDCD6IPP1","gene_name":"PDCD6IP pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49872]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100861430","summary":null,"start":22727104,"end":22744918,"strand":1,"description":"PDCD6IP pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49872]"}, {"versioned_ensembl_gene_id":"ENSG00000279638.1","gene_symbol":"AC008873.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":54286194,"end":54286331,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261504.1","gene_symbol":"LINC01686","gene_name":"long intergenic non-protein coding RNA 1686 [Source:HGNC Symbol;Acc:HGNC:27643]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284648","summary":null,"start":182615254,"end":182616629,"strand":1,"description":"long intergenic non-protein coding RNA 1686 [Source:HGNC Symbol;Acc:HGNC:27643]"}, {"versioned_ensembl_gene_id":"ENSG00000167654.17","gene_symbol":"ATCAY","gene_name":"ATCAY, caytaxin [Source:HGNC Symbol;Acc:HGNC:779]","synonyms":"BNIP-H","biotype":"protein_coding","ncbi_id":"85300","summary":"This gene encodes a neuron-restricted protein that contains a CRAL-TRIO motif common to proteins that bind small lipophilic molecules. Mutations in this gene are associated with cerebellar ataxia, Cayman type. [provided by RefSeq, Jul 2008]","start":3879864,"end":3928079,"strand":1,"description":"ATCAY, caytaxin [Source:HGNC Symbol;Acc:HGNC:779]"}, {"versioned_ensembl_gene_id":"ENSG00000228561.2","gene_symbol":"AC026355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177683627,"end":177691250,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263482.3","gene_symbol":"ANTXRLP1","gene_name":"anthrax toxin receptor-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45004]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996567","summary":null,"start":46233885,"end":46273557,"strand":-1,"description":"anthrax toxin receptor-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45004]"}, {"versioned_ensembl_gene_id":"ENSG00000226666.1","gene_symbol":"HSPA9P1","gene_name":"heat shock protein family A (Hsp70) member 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24915]","synonyms":"HSPA9P,HSPA9BP","biotype":"processed_pseudogene","ncbi_id":"266724","summary":null,"start":221961737,"end":221963765,"strand":1,"description":"heat shock protein family A (Hsp70) member 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24915]"}, {"versioned_ensembl_gene_id":"ENSG00000175302.5","gene_symbol":"ANKRD30BP1","gene_name":"ankyrin repeat domain 30B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19722]","synonyms":"PRED4,C21orf110,ANKRD30BP","biotype":"unprocessed_pseudogene","ncbi_id":"642460","summary":null,"start":13384249,"end":13427773,"strand":-1,"description":"ankyrin repeat domain 30B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19722]"}, {"versioned_ensembl_gene_id":"ENSG00000223750.1","gene_symbol":"SIRPB3P","gene_name":"signal regulatory protein beta 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:49209]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100652885","summary":null,"start":1665283,"end":1708200,"strand":-1,"description":"signal regulatory protein beta 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:49209]"}, {"versioned_ensembl_gene_id":"ENSG00000203523.3","gene_symbol":"TAS2R2P","gene_name":"taste 2 receptor member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20615]","synonyms":"TAS2R2,T2R2,T2R02","biotype":"processed_pseudogene","ncbi_id":"338396","summary":null,"start":12491095,"end":12492004,"strand":1,"description":"taste 2 receptor member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:20615]"}, {"versioned_ensembl_gene_id":"ENSG00000257095.1","gene_symbol":"AC084361.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119031039,"end":119116961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259380.5","gene_symbol":"AC087473.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38139595,"end":38226887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206107.2","gene_symbol":"KRTAP27-1","gene_name":"keratin associated protein 27-1 [Source:HGNC Symbol;Acc:HGNC:33864]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643812","summary":null,"start":30337013,"end":30337694,"strand":-1,"description":"keratin associated protein 27-1 [Source:HGNC Symbol;Acc:HGNC:33864]"}, {"versioned_ensembl_gene_id":"ENSG00000256031.2","gene_symbol":"AC087885.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":118989727,"end":119001842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133812.15","gene_symbol":"SBF2","gene_name":"SET binding factor 2 [Source:HGNC Symbol;Acc:HGNC:2135]","synonyms":"KIAA1766,DENND7B,CMT4B2,MTMR13","biotype":"protein_coding","ncbi_id":"81846","summary":"This gene encodes a pseudophosphatase and member of the myotubularin-related protein family. This gene maps within the CMT4B2 candidate region of chromosome 11p15 and mutations in this gene have been associated with Charcot-Marie-Tooth Disease, type 4B2. [provided by RefSeq, Jul 2008]","start":9778667,"end":10294207,"strand":-1,"description":"SET binding factor 2 [Source:HGNC Symbol;Acc:HGNC:2135]"}, {"versioned_ensembl_gene_id":"ENSG00000255476.1","gene_symbol":"AC011092.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9839143,"end":9929263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205642.9","gene_symbol":"VCX3B","gene_name":"variable charge, X-linked 3B [Source:HGNC Symbol;Acc:HGNC:31838]","synonyms":"VCX-C","biotype":"protein_coding","ncbi_id":"425054","summary":"This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. The X-linked members are clustered on chromosome Xp22, and the Y-linked members are two identical copies of the gene within a palindromic region on chromosome Yq11. The family members share a high degree of sequence identity, with the exception that a 30-nt unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. This family member, as represented by the reference genome allele, contains 14 copies of the 30-nt repeat unit. VCX/Y genes encode small and highly charged proteins containing putative bipartite nuclear localization signals. Although the exact function of this family member has yet to be determined, a role in mRNA stability regulation can be inferred from the ability of the highly similar family member, VCX-A, to inhibit mRNA decapping. A possible role in the regulation of ribosome assembly during spermatogenesis has also been suggested. [provided by RefSeq, Aug 2010]","start":8464830,"end":8466510,"strand":1,"description":"variable charge, X-linked 3B [Source:HGNC Symbol;Acc:HGNC:31838]"}, {"versioned_ensembl_gene_id":"ENSG00000219200.11","gene_symbol":"RNASEK","gene_name":"ribonuclease K [Source:HGNC Symbol;Acc:HGNC:33911]","synonyms":"MGC71993","biotype":"protein_coding","ncbi_id":"440400","summary":null,"start":7012417,"end":7014532,"strand":1,"description":"ribonuclease K [Source:HGNC Symbol;Acc:HGNC:33911]"}, {"versioned_ensembl_gene_id":"ENSG00000226711.6","gene_symbol":"FAM66C","gene_name":"family with sequence similarity 66 member C [Source:HGNC Symbol;Acc:HGNC:21644]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"440078","summary":null,"start":8180209,"end":8216151,"strand":1,"description":"family with sequence similarity 66 member C [Source:HGNC Symbol;Acc:HGNC:21644]"}, {"versioned_ensembl_gene_id":"ENSG00000225267.1","gene_symbol":"RPL8P2","gene_name":"ribosomal protein L8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17220]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128766","summary":null,"start":30263380,"end":30263881,"strand":-1,"description":"ribosomal protein L8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17220]"}, {"versioned_ensembl_gene_id":"ENSG00000234953.2","gene_symbol":"AL138799.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81513880,"end":81557702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278074.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803565,"end":54814279,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000015475.18","gene_symbol":"BID","gene_name":"BH3 interacting domain death agonist [Source:HGNC Symbol;Acc:HGNC:1050]","synonyms":null,"biotype":"protein_coding","ncbi_id":"637","summary":"This gene encodes a death agonist that heterodimerizes with either agonist BAX or antagonist BCL2, and thus regulate apoptosis. The encoded protein is a member of the BCL-2 family of cell death regulators. It is a mediator of mitochondrial damage induced by caspase-8 (CASP8); CASP8 cleaves this encoded protein, and the COOH-terminal part translocates to mitochondria where it triggers cytochrome c release. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Aug 2020]","start":17734138,"end":17774770,"strand":-1,"description":"BH3 interacting domain death agonist [Source:HGNC Symbol;Acc:HGNC:1050]"}, {"versioned_ensembl_gene_id":"ENSG00000163673.7","gene_symbol":"DCLK3","gene_name":"doublecortin like kinase 3 [Source:HGNC Symbol;Acc:HGNC:19005]","synonyms":"KIAA1765,DCDC3C,DCAMKL3","biotype":"protein_coding","ncbi_id":"85443","summary":null,"start":36712422,"end":36764349,"strand":-1,"description":"doublecortin like kinase 3 [Source:HGNC Symbol;Acc:HGNC:19005]"}, {"versioned_ensembl_gene_id":"ENSG00000204616.10","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"C6orf13,HCGI,HCG1,RNF","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30102897,"end":30113106,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000061676.14","gene_symbol":"NCKAP1","gene_name":"NCK associated protein 1 [Source:HGNC Symbol;Acc:HGNC:7666]","synonyms":"NAP125,Nap1,HEM2","biotype":"protein_coding","ncbi_id":"10787","summary":null,"start":182909115,"end":183038858,"strand":-1,"description":"NCK associated protein 1 [Source:HGNC Symbol;Acc:HGNC:7666]"}, {"versioned_ensembl_gene_id":"ENSG00000279450.1","gene_symbol":"AC112200.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10556582,"end":10556815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237740.1","gene_symbol":"NPAP1P3","gene_name":"nuclear pore associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45020]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420830","summary":null,"start":87376896,"end":87378481,"strand":1,"description":"nuclear pore associated protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45020]"}, {"versioned_ensembl_gene_id":"ENSG00000230732.4","gene_symbol":"AC016949.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":196912646,"end":196914579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228963.3","gene_symbol":"AF186996.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125724539,"end":125725445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248587.7","gene_symbol":"GDNF-AS1","gene_name":"GDNF antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43592]","synonyms":"GDNFOS","biotype":"antisense_RNA","ncbi_id":"100861519","summary":null,"start":37811589,"end":37953827,"strand":1,"description":"GDNF antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43592]"}, {"versioned_ensembl_gene_id":"ENSG00000179950.13","gene_symbol":"PUF60","gene_name":"poly(U) binding splicing factor 60 [Source:HGNC Symbol;Acc:HGNC:17042]","synonyms":"SIAHBP1,RoBPI,FIR","biotype":"protein_coding","ncbi_id":"22827","summary":"This gene encodes a nucleic acid-binding protein that plays a role in a variety of nuclear processes, including pre-mRNA splicing and transcriptional regulation. The encoded protein forms a complex with the far upstream DNA element (FUSE) and FUSE-binding protein at the myelocytomatosis oncogene (MYC) promoter. This complex represses MYC transcription through the core-TFIIH basal transcription factor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":143816344,"end":143829859,"strand":-1,"description":"poly(U) binding splicing factor 60 [Source:HGNC Symbol;Acc:HGNC:17042]"}, {"versioned_ensembl_gene_id":"ENSG00000111640.14","gene_symbol":"GAPDH","gene_name":"glyceraldehyde-3-phosphate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4141]","synonyms":"GAPD","biotype":"protein_coding","ncbi_id":"2597","summary":"This gene encodes a member of the glyceraldehyde-3-phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy-yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD). The encoded protein has additionally been identified to have uracil DNA glycosylase activity in the nucleus. Also, this protein contains a peptide that has antimicrobial activity against E. coli, P. aeruginosa, and C. albicans. Studies of a similar protein in mouse have assigned a variety of additional functions including nitrosylation of nuclear proteins, the regulation of mRNA stability, and acting as a transferrin receptor on the cell surface of macrophage. Many pseudogenes similar to this locus are present in the human genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":6533927,"end":6538374,"strand":1,"description":"glyceraldehyde-3-phosphate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4141]"}, {"versioned_ensembl_gene_id":"ENSG00000104213.12","gene_symbol":"PDGFRL","gene_name":"platelet derived growth factor receptor like [Source:HGNC Symbol;Acc:HGNC:8805]","synonyms":"PRLTS","biotype":"protein_coding","ncbi_id":"5157","summary":"This gene encodes a protein with significant sequence similarity to the ligand binding domain of platelet-derived growth factor receptor beta. Mutations in this gene, or deletion of a chromosomal segment containing this gene, are associated with sporadic hepatocellular carcinomas, colorectal cancers, and non-small cell lung cancers. This suggests this gene product may function as a tumor suppressor. [provided by RefSeq, Jul 2008]","start":17576433,"end":17644071,"strand":1,"description":"platelet derived growth factor receptor like [Source:HGNC Symbol;Acc:HGNC:8805]"}, {"versioned_ensembl_gene_id":"ENSG00000145491.11","gene_symbol":"ROPN1L","gene_name":"rhophilin associated tail protein 1 like [Source:HGNC Symbol;Acc:HGNC:24060]","synonyms":"RSPH11,FLJ25776,ASP","biotype":"protein_coding","ncbi_id":"83853","summary":"This gene encodes a member of the ropporin family. The encoded protein is present in sperm and interacts with A-kinase anchoring protein, AKAP3, through the amphipathic helix region of AKAP3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2014]","start":10441524,"end":10472029,"strand":1,"description":"rhophilin associated tail protein 1 like [Source:HGNC Symbol;Acc:HGNC:24060]"}, {"versioned_ensembl_gene_id":"ENSG00000244280.1","gene_symbol":"ECEL1P2","gene_name":"endothelin converting enzyme like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14019]","synonyms":"ECEL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"347694","summary":null,"start":232385750,"end":232387457,"strand":-1,"description":"endothelin converting enzyme like 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:14019]"}, {"versioned_ensembl_gene_id":"ENSG00000250600.1","gene_symbol":"ROPN1L-AS1","gene_name":"ROPN1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39984]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505845","summary":null,"start":10441290,"end":10441792,"strand":-1,"description":"ROPN1L antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39984]"}, {"versioned_ensembl_gene_id":"ENSG00000229765.2","gene_symbol":"AL354868.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10213881,"end":10214362,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167701.13","gene_symbol":"GPT","gene_name":"glutamic--pyruvic transaminase [Source:HGNC Symbol;Acc:HGNC:4552]","synonyms":"GPT1,ALT1","biotype":"protein_coding","ncbi_id":"2875","summary":"This gene encodes cytosolic alanine aminotransaminase 1 (ALT1); also known as glutamate-pyruvate transaminase 1. This enzyme catalyzes the reversible transamination between alanine and 2-oxoglutarate to generate pyruvate and glutamate and, therefore, plays a key role in the intermediary metabolism of glucose and amino acids. Serum activity levels of this enzyme are routinely used as a biomarker of liver injury caused by drug toxicity, infection, alcohol, and steatosis. A related gene on chromosome 16 encodes a putative mitochondrial alanine aminotransaminase.[provided by RefSeq, Nov 2009]","start":144502973,"end":144507174,"strand":1,"description":"glutamic--pyruvic transaminase [Source:HGNC Symbol;Acc:HGNC:4552]"}, {"versioned_ensembl_gene_id":"ENSG00000277282.1","gene_symbol":"IGHV1OR21-1","gene_name":"immunoglobulin heavy variable 1/OR21-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:38040]","synonyms":"IGHV1/OR21-1","biotype":"IG_V_gene","ncbi_id":"390530","summary":null,"start":10649400,"end":10649835,"strand":-1,"description":"immunoglobulin heavy variable 1/OR21-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:38040]"}, {"versioned_ensembl_gene_id":"ENSG00000259331.1","gene_symbol":"AC009432.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94600014,"end":94600821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255182.2","gene_symbol":"AC084125.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":144495458,"end":144505444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228630.5","gene_symbol":"HOTAIR","gene_name":"HOX transcript antisense RNA [Source:HGNC Symbol;Acc:HGNC:33510]","synonyms":"NCRNA00072,HOXC11-AS1,HOXC-AS4","biotype":"antisense_RNA","ncbi_id":"100124700","summary":"This gene is located within the Homeobox C (HOXC) gene cluster on chromosome 12 and is co-expressed with the HOXC genes. It functions through an RNA product, which binds lysine specific demethylase 1 (LSD1) and Polycomb repressive complex 2 (PRC2), and serves as a scaffold to assemble these regulators at the HOXD gene cluster, thereby promoting epigenetic repression of HOXD. This gene is highly expressed in multiple tumors. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Feb 2019]","start":53962308,"end":53974956,"strand":-1,"description":"HOX transcript antisense RNA [Source:HGNC Symbol;Acc:HGNC:33510]"}, {"versioned_ensembl_gene_id":"ENSG00000270031.1","gene_symbol":"AL020997.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27819983,"end":27820341,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278880.1","gene_symbol":"AC092608.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":156886645,"end":156886862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227406.1","gene_symbol":"RNF6P1","gene_name":"ring finger protein 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420924","summary":null,"start":39373763,"end":39377066,"strand":-1,"description":"ring finger protein 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39922]"}, {"versioned_ensembl_gene_id":"ENSG00000101888.11","gene_symbol":"NXT2","gene_name":"nuclear transport factor 2 like export factor 2 [Source:HGNC Symbol;Acc:HGNC:18151]","synonyms":"P15-2","biotype":"protein_coding","ncbi_id":"55916","summary":"The protein encoded by this gene contains a nuclear transport factor 2 (NTF2) domain, which plays an important role in the trafficking of macromolecules, ions, and small molecules between the cytoplasm and nucleus. This protein may also have a role in mRNA nuclear export. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jun 2011]","start":109535781,"end":109544690,"strand":1,"description":"nuclear transport factor 2 like export factor 2 [Source:HGNC Symbol;Acc:HGNC:18151]"}, {"versioned_ensembl_gene_id":"ENSG00000261682.1","gene_symbol":"AC145350.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33129316,"end":33134499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276556.1","gene_symbol":"AF254982.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10640028,"end":10640338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213461.3","gene_symbol":"AL672212.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41308166,"end":41308565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226308.1","gene_symbol":"AL122058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57266797,"end":57282998,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220343.5","gene_symbol":"AC092965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167065831,"end":167066320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099968.17","gene_symbol":"BCL2L13","gene_name":"BCL2 like 13 [Source:HGNC Symbol;Acc:HGNC:17164]","synonyms":"MIL1,BCL-RAMBO","biotype":"protein_coding","ncbi_id":"23786","summary":"This gene encodes a mitochondrially-localized protein with conserved B-cell lymphoma 2 homology motifs. Overexpression of the encoded protein results in apoptosis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":17628855,"end":17730855,"strand":1,"description":"BCL2 like 13 [Source:HGNC Symbol;Acc:HGNC:17164]"}, {"versioned_ensembl_gene_id":"ENSG00000268754.1","gene_symbol":"LINC01081","gene_name":"long intergenic non-protein coding RNA 1081 [Source:HGNC Symbol;Acc:HGNC:49124]","synonyms":"TCONS_00024764","biotype":"lincRNA","ncbi_id":"101154687","summary":null,"start":86225580,"end":86275745,"strand":-1,"description":"long intergenic non-protein coding RNA 1081 [Source:HGNC Symbol;Acc:HGNC:49124]"}, {"versioned_ensembl_gene_id":"ENSG00000276540.1","gene_symbol":"REXO1L10P","gene_name":"REXO1 like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:44433]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288500","summary":null,"start":85744543,"end":85748373,"strand":-1,"description":"REXO1 like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:44433]"}, {"versioned_ensembl_gene_id":"ENSG00000244036.3","gene_symbol":"AC073320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129953234,"end":130026989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272646.1","gene_symbol":"AC079766.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":182881777,"end":182882203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242326.1","gene_symbol":"AC104629.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166181313,"end":166181820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085563.14","gene_symbol":"ABCB1","gene_name":"ATP binding cassette subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:40]","synonyms":"PGY1,P-gp,MDR1,GP170,CLCS,CD243,ABC20","biotype":"protein_coding","ncbi_id":"5243","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is an ATP-dependent drug efflux pump for xenobiotic compounds with broad substrate specificity. It is responsible for decreased drug accumulation in multidrug-resistant cells and often mediates the development of resistance to anticancer drugs. This protein also functions as a transporter in the blood-brain barrier. Mutations in this gene are associated with colchicine resistance and Inflammatory bowel disease 13. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":87503633,"end":87713323,"strand":-1,"description":"ATP binding cassette subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:40]"}, {"versioned_ensembl_gene_id":"ENSG00000111218.11","gene_symbol":"PRMT8","gene_name":"protein arginine methyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:5188]","synonyms":"HRMT1L3,HRMT1L4","biotype":"protein_coding","ncbi_id":"56341","summary":"Arginine methylation is a widespread posttranslational modification mediated by arginine methyltransferases, such as PRMT8. Arginine methylation is involved in a number of cellular processes, including DNA repair, RNA transcription, signal transduction, protein compartmentalization, and possibly protein translation (Lee et al., 2005 [PubMed 16051612]).[supplied by OMIM, Mar 2008]","start":3381349,"end":3593973,"strand":1,"description":"protein arginine methyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:5188]"}, {"versioned_ensembl_gene_id":"ENSG00000123552.17","gene_symbol":"USP45","gene_name":"ubiquitin specific peptidase 45 [Source:HGNC Symbol;Acc:HGNC:20080]","synonyms":"MGC14793","biotype":"protein_coding","ncbi_id":"85015","summary":"The protein encoded by this gene is a deubiquitylase that binds ERCC1, the catalytic subunit of the XPF-ERCC1 DNA repair endonuclease. This endonuclease is a critical regulator of DNA repair processes, and the deubiquitylase activity of the encoded protein is important for maintaining the DNA repair ability of XPF-ERCC1. [provided by RefSeq, Sep 2016]","start":99432379,"end":99521728,"strand":-1,"description":"ubiquitin specific peptidase 45 [Source:HGNC Symbol;Acc:HGNC:20080]"}, {"versioned_ensembl_gene_id":"ENSG00000234358.1","gene_symbol":"AC003080.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111971222,"end":111971988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263242.2","gene_symbol":"KRTAP1-4","gene_name":"keratin associated protein 1-4 [Source:HGNC Symbol;Acc:HGNC:18904]","synonyms":"KAP1.4","biotype":"protein_coding","ncbi_id":"728255","summary":"The main structural proteins of mammalian hair fiber are the hair keratins (see MIM 601077) and the keratin-associated proteins (KAPs), which form a rigid and resistant hair shaft through extensive disulfide bond crosslinking with the abundant cysteines of hair keratins (Shimomura et al., 2002 [PubMed 12228244]).[supplied by OMIM, Jan 2009]","start":41029824,"end":41030231,"strand":-1,"description":"keratin associated protein 1-4 [Source:HGNC Symbol;Acc:HGNC:18904]"}, {"versioned_ensembl_gene_id":"ENSG00000260900.1","gene_symbol":"AC145350.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33059936,"end":33060098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218689.2","gene_symbol":"RPL5P21","gene_name":"ribosomal protein L5 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37029]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270838","summary":null,"start":129756298,"end":129757112,"strand":-1,"description":"ribosomal protein L5 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37029]"}, {"versioned_ensembl_gene_id":"ENSG00000114023.15","gene_symbol":"FAM162A","gene_name":"family with sequence similarity 162 member A [Source:HGNC Symbol;Acc:HGNC:17865]","synonyms":"E2IG5,C3orf28","biotype":"protein_coding","ncbi_id":"26355","summary":null,"start":122384176,"end":122412334,"strand":1,"description":"family with sequence similarity 162 member A [Source:HGNC Symbol;Acc:HGNC:17865]"}, {"versioned_ensembl_gene_id":"ENSG00000257839.1","gene_symbol":"AC011611.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":76032658,"end":76033897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239470.3","gene_symbol":"AC011979.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9660438,"end":9660920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248751.6","gene_symbol":"AC004997.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30285238,"end":30299482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166200.14","gene_symbol":"COPS2","gene_name":"COP9 signalosome subunit 2 [Source:HGNC Symbol;Acc:HGNC:30747]","synonyms":"TRIP15,CSN2,ALIEN","biotype":"protein_coding","ncbi_id":"9318","summary":null,"start":49106068,"end":49155661,"strand":-1,"description":"COP9 signalosome subunit 2 [Source:HGNC Symbol;Acc:HGNC:30747]"}, {"versioned_ensembl_gene_id":"ENSG00000187733.6","gene_symbol":"AMY1C","gene_name":"amylase, alpha 1C (salivary) [Source:HGNC Symbol;Acc:HGNC:476]","synonyms":"AMY1","biotype":"protein_coding","ncbi_id":"278","summary":"Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the salivary gland. [provided by RefSeq, Jul 2008]","start":103750406,"end":103758690,"strand":1,"description":"amylase, alpha 1C (salivary) [Source:HGNC Symbol;Acc:HGNC:476]"}, {"versioned_ensembl_gene_id":"ENSG00000162594.15","gene_symbol":"IL23R","gene_name":"interleukin 23 receptor [Source:HGNC Symbol;Acc:HGNC:19100]","synonyms":"IL-23R","biotype":"protein_coding","ncbi_id":"149233","summary":"The protein encoded by this gene is a subunit of the receptor for IL23A/IL23. This protein pairs with the receptor molecule IL12RB1/IL12Rbeta1, and both are required for IL23A signaling. This protein associates constitutively with Janus kinase 2 (JAK2), and also binds to transcription activator STAT3 in a ligand-dependent manner. [provided by RefSeq, Jul 2008]","start":67138907,"end":67259979,"strand":1,"description":"interleukin 23 receptor [Source:HGNC Symbol;Acc:HGNC:19100]"}, {"versioned_ensembl_gene_id":"ENSG00000275580.1","gene_symbol":"AC022306.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49343608,"end":49344254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171659.13","gene_symbol":"GPR34","gene_name":"G protein-coupled receptor 34 [Source:HGNC Symbol;Acc:HGNC:4490]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2857","summary":"G protein-coupled receptors (GPCRs), such as GPR34, are integral membrane proteins containing 7 putative transmembrane domains (TMs). These proteins mediate signals to the interior of the cell via activation of heterotrimeric G proteins that in turn activate various effector proteins, ultimately resulting in a physiologic response.[supplied by OMIM, Apr 2006]","start":41688973,"end":41697277,"strand":1,"description":"G protein-coupled receptor 34 [Source:HGNC Symbol;Acc:HGNC:4490]"}, {"versioned_ensembl_gene_id":"ENSG00000279903.1","gene_symbol":"AP006248.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17500012,"end":17500605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197627.3","gene_symbol":"UBE2Q2P12","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49523]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421768","summary":null,"start":84491480,"end":84500599,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49523]"}, {"versioned_ensembl_gene_id":"ENSG00000250993.1","gene_symbol":"AC020551.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179389134,"end":179465305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227817.4","gene_symbol":"ARHGAP42P1","gene_name":"Rho GTPase activating protein 42 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43940]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100887075","summary":null,"start":131328176,"end":131330857,"strand":-1,"description":"Rho GTPase activating protein 42 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43940]"}, {"versioned_ensembl_gene_id":"ENSG00000226332.2","gene_symbol":"AL354836.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62305432,"end":62306325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235960.9","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"RNF93,ZNFB7,ZNF178","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30153514,"end":30163004,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000224425.2","gene_symbol":"AC073869.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131352214,"end":131353239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115008.5","gene_symbol":"IL1A","gene_name":"interleukin 1 alpha [Source:HGNC Symbol;Acc:HGNC:5991]","synonyms":"IL1F1,IL1-ALPHA,IL1,IL-1A","biotype":"protein_coding","ncbi_id":"3552","summary":"The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine is a pleiotropic cytokine involved in various immune responses, inflammatory processes, and hematopoiesis. This cytokine is produced by monocytes and macrophages as a proprotein, which is proteolytically processed and released in response to cell injury, and thus induces apoptosis. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. It has been suggested that the polymorphism of these genes is associated with rheumatoid arthritis and Alzheimer's disease. [provided by RefSeq, Jul 2008]","start":112773915,"end":112784590,"strand":-1,"description":"interleukin 1 alpha [Source:HGNC Symbol;Acc:HGNC:5991]"}, {"versioned_ensembl_gene_id":"ENSG00000105639.18","gene_symbol":"JAK3","gene_name":"Janus kinase 3 [Source:HGNC Symbol;Acc:HGNC:6193]","synonyms":"LJAK,L-JAK,JAKL,JAK3_HUMAN,JAK-3","biotype":"protein_coding","ncbi_id":"3718","summary":"The protein encoded by this gene is a member of the Janus kinase (JAK) family of tyrosine kinases involved in cytokine receptor-mediated intracellular signal transduction. It is predominantly expressed in immune cells and transduces a signal in response to its activation via tyrosine phosphorylation by interleukin receptors. Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease). [provided by RefSeq, Jul 2008]","start":17824780,"end":17848071,"strand":-1,"description":"Janus kinase 3 [Source:HGNC Symbol;Acc:HGNC:6193]"}, {"versioned_ensembl_gene_id":"ENSG00000225448.1","gene_symbol":"AC009477.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131181153,"end":131181369,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240100.1","gene_symbol":"AC083806.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116908312,"end":116908627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284604.1","gene_symbol":"AC073869.8","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":131303037,"end":131355683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231431.7","gene_symbol":"FAR2P4","gene_name":"fatty acyl-CoA reductase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49286]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100420005","summary":null,"start":131279290,"end":131309068,"strand":1,"description":"fatty acyl-CoA reductase 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49286]"}, {"versioned_ensembl_gene_id":"ENSG00000099992.15","gene_symbol":"TBC1D10A","gene_name":"TBC1 domain family member 10A [Source:HGNC Symbol;Acc:HGNC:23609]","synonyms":"TBC1D10,EPI64,AC004997.C22.2","biotype":"protein_coding","ncbi_id":"83874","summary":null,"start":30291990,"end":30327046,"strand":-1,"description":"TBC1 domain family member 10A [Source:HGNC Symbol;Acc:HGNC:23609]"}, {"versioned_ensembl_gene_id":"ENSG00000188643.10","gene_symbol":"S100A16","gene_name":"S100 calcium binding protein A16 [Source:HGNC Symbol;Acc:HGNC:20441]","synonyms":"S100F,MGC17528,DT1P1A7","biotype":"protein_coding","ncbi_id":"140576","summary":null,"start":153606886,"end":153613145,"strand":-1,"description":"S100 calcium binding protein A16 [Source:HGNC Symbol;Acc:HGNC:20441]"}, {"versioned_ensembl_gene_id":"ENSG00000228506.1","gene_symbol":"AL513550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99424922,"end":99431373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132424.14","gene_symbol":"PNISR","gene_name":"PNN interacting serine and arginine rich protein [Source:HGNC Symbol;Acc:HGNC:21222]","synonyms":"SRrp130,SFRS18,FLJ14752,DKFZp564B0769,C6orf111,bA98I9.2","biotype":"protein_coding","ncbi_id":"25957","summary":null,"start":99398051,"end":99425331,"strand":-1,"description":"PNN interacting serine and arginine rich protein [Source:HGNC Symbol;Acc:HGNC:21222]"}, {"versioned_ensembl_gene_id":"ENSG00000259728.5","gene_symbol":"LINC00933","gene_name":"long intergenic non-protein coding RNA 933 [Source:HGNC Symbol;Acc:HGNC:48625]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100506874","summary":null,"start":84570649,"end":84580175,"strand":1,"description":"long intergenic non-protein coding RNA 933 [Source:HGNC Symbol;Acc:HGNC:48625]"}, {"versioned_ensembl_gene_id":"ENSG00000256304.1","gene_symbol":"CCDC150P1","gene_name":"coiled-coil domain containing 150 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420678","summary":null,"start":122322122,"end":122324336,"strand":-1,"description":"coiled-coil domain containing 150 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50280]"}, {"versioned_ensembl_gene_id":"ENSG00000270434.1","gene_symbol":"AC012044.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45812648,"end":45812944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280453.1","gene_symbol":"AP006248.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17498737,"end":17499157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241877.1","gene_symbol":"AC095041.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178286695,"end":178287285,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279932.1","gene_symbol":"AP006248.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17510613,"end":17511300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231122.5","gene_symbol":"FAM25E","gene_name":"family with sequence similarity 25 member E [Source:HGNC Symbol;Acc:HGNC:23587]","synonyms":"FAM25D,bA592B15.5,AC012044.5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643479","summary":null,"start":45815428,"end":45817324,"strand":-1,"description":"family with sequence similarity 25 member E [Source:HGNC Symbol;Acc:HGNC:23587]"}, {"versioned_ensembl_gene_id":"ENSG00000250839.1","gene_symbol":"AC018710.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":179069437,"end":179069594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263070.1","gene_symbol":"AC019322.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30380353,"end":30386987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174599.5","gene_symbol":"TRAM1L1","gene_name":"translocation associated membrane protein 1-like 1 [Source:HGNC Symbol;Acc:HGNC:28371]","synonyms":"MGC26568","biotype":"protein_coding","ncbi_id":"133022","summary":null,"start":117083554,"end":117085576,"strand":-1,"description":"translocation associated membrane protein 1-like 1 [Source:HGNC Symbol;Acc:HGNC:28371]"}, {"versioned_ensembl_gene_id":"ENSG00000206383.8","gene_symbol":"HSPA1L","gene_name":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]","synonyms":"hum70t,HSP70-HOM","biotype":"protein_coding","ncbi_id":"3305","summary":"This gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein. [provided by RefSeq, Jul 2008]","start":31799855,"end":31805300,"strand":-1,"description":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]"}, {"versioned_ensembl_gene_id":"ENSG00000261559.1","gene_symbol":"FSCN1P1","gene_name":"fascin actin-bundling protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49669]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"145989","summary":null,"start":34494420,"end":34495900,"strand":1,"description":"fascin actin-bundling protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49669]"}, {"versioned_ensembl_gene_id":"ENSG00000279378.1","gene_symbol":"AC009159.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":79675685,"end":79677715,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224550.1","gene_symbol":"AC114491.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107505203,"end":107505448,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276240.2","gene_symbol":"OR4E1","gene_name":"olfactory receptor family 4 subfamily E member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8296]","synonyms":"OR4E1P","biotype":"polymorphic_pseudogene","ncbi_id":"26687","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21667940,"end":21673818,"strand":-1,"description":"olfactory receptor family 4 subfamily E member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8296]"}, {"versioned_ensembl_gene_id":"ENSG00000235175.1","gene_symbol":"RPL26P37","gene_name":"ribosomal protein L26 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441533","summary":null,"start":5793300,"end":5793737,"strand":-1,"description":"ribosomal protein L26 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:36004]"}, {"versioned_ensembl_gene_id":"ENSG00000215559.8","gene_symbol":"ANKRD20A11P","gene_name":"ankyrin repeat domain 20 family member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:42024]","synonyms":"C21orf81","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"391267","summary":null,"start":13909574,"end":13980437,"strand":-1,"description":"ankyrin repeat domain 20 family member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:42024]"}, {"versioned_ensembl_gene_id":"ENSG00000122735.15","gene_symbol":"DNAI1","gene_name":"dynein axonemal intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2954]","synonyms":"PCD,DIC1,CILD1","biotype":"protein_coding","ncbi_id":"27019","summary":"This gene encodes a member of the dynein intermediate chain family. The encoded protein is part of the dynein complex in respiratory cilia. The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia and Kartagener syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":34457414,"end":34520989,"strand":1,"description":"dynein axonemal intermediate chain 1 [Source:HGNC Symbol;Acc:HGNC:2954]"}, {"versioned_ensembl_gene_id":"ENSG00000102230.13","gene_symbol":"PCYT1B","gene_name":"phosphate cytidylyltransferase 1, choline, beta [Source:HGNC Symbol;Acc:HGNC:8755]","synonyms":"CTB,CCT-beta","biotype":"protein_coding","ncbi_id":"9468","summary":"The protein encoded by this gene belongs to the cytidylyltransferase family. It is involved in the regulation of phosphatidylcholine biosynthesis. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":24558087,"end":24672677,"strand":-1,"description":"phosphate cytidylyltransferase 1, choline, beta [Source:HGNC Symbol;Acc:HGNC:8755]"}, {"versioned_ensembl_gene_id":"ENSG00000214125.2","gene_symbol":"AC005005.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31155966,"end":31156647,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272334.1","gene_symbol":"AC011816.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36973117,"end":36973672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171121.16","gene_symbol":"KCNMB3","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:6287]","synonyms":"KCNMBL,KCNMB2","biotype":"protein_coding","ncbi_id":"27094","summary":"MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit and the modulatory beta subunit. The protein encoded by this gene is an auxiliary beta subunit which may partially inactivate or slightly decrease the activation time of MaxiK alpha subunit currents. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 22. [provided by RefSeq, Jul 2009]","start":179236691,"end":179267002,"strand":-1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:6287]"}, {"versioned_ensembl_gene_id":"ENSG00000147434.8","gene_symbol":"CHRNA6","gene_name":"cholinergic receptor nicotinic alpha 6 subunit [Source:HGNC Symbol;Acc:HGNC:15963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8973","summary":"This gene encodes an alpha subunit of neuronal nicotinic acetylcholine receptors. These receptors consist of five subunits and function as ion channels involved in neurotransmission. The encoded protein is a subunit of neuronal nicotinic acetylcholine receptors that mediate dopaminergic neurotransmission and are activated by acetylcholine and exogenous nicotine. Alternatively spliced transcript variants have been observed for this gene. Single nucleotide polymorphisms in this gene have been associated with both nicotine and alcohol dependence. [provided by RefSeq, Dec 2010]","start":42752620,"end":42796392,"strand":-1,"description":"cholinergic receptor nicotinic alpha 6 subunit [Source:HGNC Symbol;Acc:HGNC:15963]"}, {"versioned_ensembl_gene_id":"ENSG00000277868.4","gene_symbol":"CCDC125","gene_name":"coiled-coil domain containing 125 [Source:HGNC Symbol;Acc:HGNC:28924]","synonyms":"KENAE","biotype":"protein_coding","ncbi_id":"202243","summary":null,"start":69281282,"end":69332741,"strand":-1,"description":"coiled-coil domain containing 125 [Source:HGNC Symbol;Acc:HGNC:28924]"}, {"versioned_ensembl_gene_id":"ENSG00000102010.14","gene_symbol":"BMX","gene_name":"BMX non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1079]","synonyms":"PSCTK3,ETK","biotype":"protein_coding","ncbi_id":"660","summary":"This gene encodes a non-receptor tyrosine kinase belonging to the Tec kinase family. The protein contains a PH-like domain, which mediates membrane targeting by binding to phosphatidylinositol 3,4,5-triphosphate (PIP3), and a SH2 domain that binds to tyrosine-phosphorylated proteins and functions in signal transduction. The protein is implicated in several signal transduction pathways including the Stat pathway, and regulates differentiation and tumorigenicity of several types of cancer cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]","start":15464246,"end":15556529,"strand":1,"description":"BMX non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:1079]"}, {"versioned_ensembl_gene_id":"ENSG00000215873.2","gene_symbol":"FEN1P1","gene_name":"flap structure-specific endonuclease 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3651]","synonyms":"FENL1","biotype":"processed_pseudogene","ncbi_id":"645931","summary":null,"start":91328369,"end":91329513,"strand":1,"description":"flap structure-specific endonuclease 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3651]"}, {"versioned_ensembl_gene_id":"ENSG00000272030.1","gene_symbol":"AL162258.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153631438,"end":153634397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228854.8","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30751961,"end":30755334,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000230489.1","gene_symbol":"VAV3-AS1","gene_name":"VAV3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40608]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873946","summary":null,"start":107964443,"end":107994607,"strand":1,"description":"VAV3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40608]"}, {"versioned_ensembl_gene_id":"ENSG00000229785.1","gene_symbol":"SLC25A38P1","gene_name":"solute carrier family 25 member 38 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43858]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441915","summary":null,"start":172748560,"end":172749502,"strand":1,"description":"solute carrier family 25 member 38 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43858]"}, {"versioned_ensembl_gene_id":"ENSG00000251161.3","gene_symbol":"AC020661.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40906811,"end":40910337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230568.1","gene_symbol":"SF3A3P1","gene_name":"splicing factor 3a, subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16576]","synonyms":"SF3A3P,dJ581P3.1","biotype":"processed_pseudogene","ncbi_id":"170548","summary":null,"start":3489529,"end":3491005,"strand":-1,"description":"splicing factor 3a, subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16576]"}, {"versioned_ensembl_gene_id":"ENSG00000249807.1","gene_symbol":"AC034229.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10137138,"end":10138365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117751.17","gene_symbol":"PPP1R8","gene_name":"protein phosphatase 1 regulatory subunit 8 [Source:HGNC Symbol;Acc:HGNC:9296]","synonyms":"PRO2047,NIPP1,NIPP-1,ARD1,ard-1","biotype":"protein_coding","ncbi_id":"5511","summary":"This gene, through alternative splicing, encodes three different isoforms. Two of the protein isoforms encoded by this gene are specific inhibitors of type 1 serine/threonine protein phosphatases and can bind but not cleave RNA. The third protein isoform lacks the phosphatase inhibitory function but is a single-strand endoribonuclease comparable to RNase E of E. coli. This isoform requires magnesium for its function and cleaves specific sites in A+U-rich regions of RNA. [provided by RefSeq, Jul 2008]","start":27830778,"end":27851676,"strand":1,"description":"protein phosphatase 1 regulatory subunit 8 [Source:HGNC Symbol;Acc:HGNC:9296]"}, {"versioned_ensembl_gene_id":"ENSG00000234480.1","gene_symbol":"MTCO2P18","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52034]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075149","summary":null,"start":131381840,"end":131382497,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52034]"}, {"versioned_ensembl_gene_id":"ENSG00000198844.10","gene_symbol":"ARHGEF15","gene_name":"Rho guanine nucleotide exchange factor 15 [Source:HGNC Symbol;Acc:HGNC:15590]","synonyms":"Vsm-RhoGEF,MGC44868,KIAA0915,FLJ13791,ARGEF15","biotype":"protein_coding","ncbi_id":"22899","summary":"Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein-coupled receptors. This gene encodes a protein that functions as a specific guanine nucleotide exchange factor for RhoA. It also interacts with ephrin A4 in vascular smooth muscle cells. Two alternatively spliced transcripts variants that encode the same protein have been found for this gene. [provided by RefSeq, Aug 2010]","start":8310241,"end":8322516,"strand":1,"description":"Rho guanine nucleotide exchange factor 15 [Source:HGNC Symbol;Acc:HGNC:15590]"}, {"versioned_ensembl_gene_id":"ENSG00000258104.1","gene_symbol":"HIGD1AP9","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:43004]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874452","summary":null,"start":49619334,"end":49619612,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:43004]"}, {"versioned_ensembl_gene_id":"ENSG00000263207.2","gene_symbol":"AC109462.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55332355,"end":55332967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283423.1","gene_symbol":"AC109462.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55321575,"end":55322686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240684.1","gene_symbol":"CR753846.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32635122,"end":32637710,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259462.2","gene_symbol":"CPEB1-AS1","gene_name":"CPEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27523]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"283692","summary":null,"start":82647770,"end":82692820,"strand":1,"description":"CPEB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27523]"}, {"versioned_ensembl_gene_id":"ENSG00000182054.9","gene_symbol":"IDH2","gene_name":"isocitrate dehydrogenase (NADP(+)) 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:5383]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3418","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer. The protein encoded by this gene is the NADP(+)-dependent isocitrate dehydrogenase found in the mitochondria. It plays a role in intermediary metabolism and energy production. This protein may tightly associate or interact with the pyruvate dehydrogenase complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":90083045,"end":90102504,"strand":-1,"description":"isocitrate dehydrogenase (NADP(+)) 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:5383]"}, {"versioned_ensembl_gene_id":"ENSG00000107929.14","gene_symbol":"LARP4B","gene_name":"La ribonucleoprotein domain family member 4B [Source:HGNC Symbol;Acc:HGNC:28987]","synonyms":"LARP5,KIAA0217","biotype":"protein_coding","ncbi_id":"23185","summary":"This gene encodes a member of an evolutionarily conserved protein family implicated in RNA metabolism and translation. Members of this family are characterized by the presence of an La motif, which is often located adjacent to one or more RNA recognition motifs (RRM). Together, the two motifs constitute the functional region of the protein and enable its interaction with the RNA substrate. This protein family is divided into five sub-families: the genuine La proteins and four La-related protein (LARP) sub-families. The protein encoded by this gene belongs to LARP sub-family 4. It is a cytoplasmic protein that may play a stimulatory role in translation. [provided by RefSeq, Oct 2012]","start":806914,"end":931705,"strand":-1,"description":"La ribonucleoprotein domain family member 4B [Source:HGNC Symbol;Acc:HGNC:28987]"}, {"versioned_ensembl_gene_id":"ENSG00000260145.1","gene_symbol":"AC023825.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57052505,"end":57058497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259334.1","gene_symbol":"LINC00596","gene_name":"long intergenic non-protein coding RNA 596 [Source:HGNC Symbol;Acc:HGNC:23167]","synonyms":"CNSLT1I7G,C14orf165","biotype":"lincRNA","ncbi_id":"102724845","summary":null,"start":23922247,"end":23934568,"strand":-1,"description":"long intergenic non-protein coding RNA 596 [Source:HGNC Symbol;Acc:HGNC:23167]"}, {"versioned_ensembl_gene_id":"ENSG00000258887.3","gene_symbol":"AL160237.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23817281,"end":23827396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233209.6","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"HLA-DQB,CELIAC1,IDDM1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32634703,"end":32644644,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000250693.2","gene_symbol":"RPF2P2","gene_name":"ribosome production factor 2 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44015]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128462","summary":null,"start":115628812,"end":115629707,"strand":1,"description":"ribosome production factor 2 homolog pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44015]"}, {"versioned_ensembl_gene_id":"ENSG00000259867.5","gene_symbol":"AC105411.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":80155053,"end":80563135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249081.1","gene_symbol":"OR5M14P","gene_name":"olfactory receptor family 5 subfamily M member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:15057]","synonyms":"OR5M15P","biotype":"unprocessed_pseudogene","ncbi_id":"81421","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":41722538,"end":41723512,"strand":-1,"description":"olfactory receptor family 5 subfamily M member 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:15057]"}, {"versioned_ensembl_gene_id":"ENSG00000223886.3","gene_symbol":"AC073073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105530209,"end":105530671,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225046.2","gene_symbol":"AL035423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130330857,"end":130331069,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145431.10","gene_symbol":"PDGFC","gene_name":"platelet derived growth factor C [Source:HGNC Symbol;Acc:HGNC:8801]","synonyms":"fallotein,SCDGF","biotype":"protein_coding","ncbi_id":"56034","summary":"The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a core motif of eight cysteines. This gene product appears to form only homodimers. It differs from the platelet-derived growth factor alpha and beta polypeptides in having an unusual N-terminal domain, the CUB domain. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]","start":156760454,"end":156971394,"strand":-1,"description":"platelet derived growth factor C [Source:HGNC Symbol;Acc:HGNC:8801]"}, {"versioned_ensembl_gene_id":"ENSG00000128915.11","gene_symbol":"ICE2","gene_name":"interactor of little elongation complex ELL subunit 2 [Source:HGNC Symbol;Acc:HGNC:29885]","synonyms":"NARG2,FLJ11896,BRCC1","biotype":"protein_coding","ncbi_id":"79664","summary":"This gene encodes a protein component of the little elongation complex (LEC), which plays a role in small nuclear RNA (snRNA) transcription. The LEC regulates snRNA transcription by enhancing both RNA Polymerase II occupancy and transcriptional elongation. The encoded protein and other LEC components have been shown to localize to Cajal bodies, which are sites of ribonucleoprotein (RNP) complex assembly. Pseudogenes of this gene have been identified on chromosomes 3 and 4. [provided by RefSeq, May 2017]","start":60419609,"end":60479160,"strand":-1,"description":"interactor of little elongation complex ELL subunit 2 [Source:HGNC Symbol;Acc:HGNC:29885]"}, {"versioned_ensembl_gene_id":"ENSG00000226531.2","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"G4,D6S53E","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31734577,"end":31737051,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000223751.1","gene_symbol":"AC116609.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":742488,"end":747767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272765.2","gene_symbol":"NDUFA6","gene_name":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]","synonyms":"LYRM6,CI-B14,B14,NADHB14","biotype":"protein_coding","ncbi_id":"4700","summary":"This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016]","start":42085525,"end":42090955,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]"}, {"versioned_ensembl_gene_id":"ENSG00000270880.1","gene_symbol":"AC128687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113984037,"end":113984655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065054.13","gene_symbol":"SLC9A3R2","gene_name":"SLC9A3 regulator 2 [Source:HGNC Symbol;Acc:HGNC:11076]","synonyms":"TKA-1,SIP-1,NHERF-2,E3KARP","biotype":"protein_coding","ncbi_id":"9351","summary":"This gene encodes a member of the NHERF family of PDZ scaffolding proteins. These proteins mediate many cellular processes by binding to and regulating the membrane expression and protein-protein interactions of membrane receptors and transport proteins. The encoded protein plays a role in intestinal sodium absorption by regulating the activity of the sodium/hydrogen exchanger 3, and may also regulate the cystic fibrosis transmembrane regulator (CFTR) ion channel. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":2025356,"end":2039026,"strand":1,"description":"SLC9A3 regulator 2 [Source:HGNC Symbol;Acc:HGNC:11076]"}, {"versioned_ensembl_gene_id":"ENSG00000164318.17","gene_symbol":"EGFLAM","gene_name":"EGF like, fibronectin type III and laminin G domains [Source:HGNC Symbol;Acc:HGNC:26810]","synonyms":"AGRNL,AGRINL,PIKA,FLJ39155","biotype":"protein_coding","ncbi_id":"133584","summary":null,"start":38258409,"end":38465021,"strand":1,"description":"EGF like, fibronectin type III and laminin G domains [Source:HGNC Symbol;Acc:HGNC:26810]"}, {"versioned_ensembl_gene_id":"ENSG00000224616.1","gene_symbol":"RTCA-AS1","gene_name":"RTCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50573]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506007","summary":null,"start":100264009,"end":100266120,"strand":-1,"description":"RTCA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50573]"}, {"versioned_ensembl_gene_id":"ENSG00000256385.1","gene_symbol":"UBE2NP1","gene_name":"ubiquitin conjugating enzyme E2 N pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20337]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288613","summary":null,"start":21611924,"end":21612381,"strand":-1,"description":"ubiquitin conjugating enzyme E2 N pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:20337]"}, {"versioned_ensembl_gene_id":"ENSG00000260990.1","gene_symbol":"Z94057.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":175307218,"end":175335459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273586.2","gene_symbol":"OR10G1P","gene_name":"olfactory receptor family 10 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8169]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"26540","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21601882,"end":21602825,"strand":-1,"description":"olfactory receptor family 10 subfamily G member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8169]"}, {"versioned_ensembl_gene_id":"ENSG00000232393.1","gene_symbol":"RPL5P6","gene_name":"ribosomal protein L5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35890]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646784","summary":null,"start":91023919,"end":91024804,"strand":1,"description":"ribosomal protein L5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35890]"}, {"versioned_ensembl_gene_id":"ENSG00000223710.1","gene_symbol":"CRYGGP","gene_name":"crystallin gamma G, pseudogene [Source:HGNC Symbol;Acc:HGNC:2414]","synonyms":"CRYGGP1","biotype":"unprocessed_pseudogene","ncbi_id":"1424","summary":null,"start":51775258,"end":51775402,"strand":-1,"description":"crystallin gamma G, pseudogene [Source:HGNC Symbol;Acc:HGNC:2414]"}, {"versioned_ensembl_gene_id":"ENSG00000257096.1","gene_symbol":"AL161747.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21521083,"end":21522660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270040.1","gene_symbol":"AL356055.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":39206512,"end":39206957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223788.4","gene_symbol":"DIS3L2P1","gene_name":"DIS3 like 3'-5' exoribonuclease 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14021]","synonyms":"FAM6B,DIS3L2P","biotype":"unprocessed_pseudogene","ncbi_id":"282697","summary":null,"start":232442034,"end":232447418,"strand":1,"description":"DIS3 like 3'-5' exoribonuclease 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14021]"}, {"versioned_ensembl_gene_id":"ENSG00000237087.1","gene_symbol":"AC068134.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":232420661,"end":232421461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165821.11","gene_symbol":"SALL2","gene_name":"spalt like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10526]","synonyms":"ZNF795,KIAA0360,Hsal2","biotype":"protein_coding","ncbi_id":"6297","summary":"This gene encodes a protein containing multiple zinc finger domains. The encoded protein functions in optical fissure closure during development of the eye in the embryo. Mutations in this gene are associated with ocular coloboma. [provided by RefSeq, Jul 2016]","start":21521081,"end":21537216,"strand":-1,"description":"spalt like transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10526]"}, {"versioned_ensembl_gene_id":"ENSG00000232409.1","gene_symbol":"AC019185.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208516908,"end":208517230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236474.1","gene_symbol":"GCNT1P1","gene_name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16532]","synonyms":"GCNT1P,bA189K21.2","biotype":"processed_pseudogene","ncbi_id":"170517","summary":null,"start":18420160,"end":18421454,"strand":-1,"description":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16532]"}, {"versioned_ensembl_gene_id":"ENSG00000276013.1","gene_symbol":"GU182357.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54799595,"end":54812147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147223.5","gene_symbol":"RIPPLY1","gene_name":"ripply transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:25117]","synonyms":null,"biotype":"protein_coding","ncbi_id":"92129","summary":"This gene encodes a protein similar to a zebrafish protein which acts as a transcriptional repressor in and is required for somite segmentation in zebrafish embryos (PMID: 16326386). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":106900063,"end":106903335,"strand":-1,"description":"ripply transcriptional repressor 1 [Source:HGNC Symbol;Acc:HGNC:25117]"}, {"versioned_ensembl_gene_id":"ENSG00000111725.10","gene_symbol":"PRKAB1","gene_name":"protein kinase AMP-activated non-catalytic subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9378]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5564","summary":"The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit may be a positive regulator of AMPK activity. The myristoylation and phosphorylation of this subunit have been shown to affect the enzyme activity and cellular localization of AMPK. This subunit may also serve as an adaptor molecule mediating the association of the AMPK complex. [provided by RefSeq, Jul 2008]","start":119667753,"end":119681630,"strand":1,"description":"protein kinase AMP-activated non-catalytic subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:9378]"}, {"versioned_ensembl_gene_id":"ENSG00000276979.5","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54446939,"end":54458015,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000204264.8","gene_symbol":"PSMB8","gene_name":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]","synonyms":"beta5i,LMP7,RING10,D6S216E,PSMB5i","biotype":"protein_coding","ncbi_id":"5696","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. This gene is located in the class II region of the MHC (major histocompatibility complex). Expression of this gene is induced by gamma interferon and this gene product replaces catalytic subunit 3 (proteasome beta 5 subunit) in the immunoproteasome. Proteolytic processing is required to generate a mature subunit. Two alternative transcripts encoding two isoforms have been identified; both isoforms are processed to yield the same mature subunit. [provided by RefSeq, Jul 2008]","start":32840717,"end":32844703,"strand":-1,"description":"proteasome subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:9545]"}, {"versioned_ensembl_gene_id":"ENSG00000178573.6","gene_symbol":"MAF","gene_name":"MAF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:6776]","synonyms":"c-MAF","biotype":"protein_coding","ncbi_id":"4094","summary":"The protein encoded by this gene is a DNA-binding, leucine zipper-containing transcription factor that acts as a homodimer or as a heterodimer. Depending on the binding site and binding partner, the encoded protein can be a transcriptional activator or repressor. This protein plays a role in the regulation of several cellular processes, including embryonic lens fiber cell development, increased T-cell susceptibility to apoptosis, and chondrocyte terminal differentiation. Defects in this gene are a cause of juvenile-onset pulverulent cataract as well as congenital cerulean cataract 4 (CCA4). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":79585843,"end":79600714,"strand":-1,"description":"MAF bZIP transcription factor [Source:HGNC Symbol;Acc:HGNC:6776]"}, {"versioned_ensembl_gene_id":"ENSG00000206104.2","gene_symbol":"KRTAP20-3","gene_name":"keratin associated protein 20-3 [Source:HGNC Symbol;Acc:HGNC:34001]","synonyms":"KRTAP19P4,KAP20.3,KAP19D","biotype":"protein_coding","ncbi_id":"337985","summary":null,"start":30642864,"end":30643136,"strand":1,"description":"keratin associated protein 20-3 [Source:HGNC Symbol;Acc:HGNC:34001]"}, {"versioned_ensembl_gene_id":"ENSG00000213658.11","gene_symbol":"LAT","gene_name":"linker for activation of T-cells [Source:HGNC Symbol;Acc:HGNC:18874]","synonyms":"LAT1","biotype":"protein_coding","ncbi_id":"27040","summary":"The protein encoded by this gene is phosphorylated by ZAP-70/Syk protein tyrosine kinases following activation of the T-cell antigen receptor (TCR) signal transduction pathway. This transmembrane protein localizes to lipid rafts and acts as a docking site for SH2 domain-containing proteins. Upon phosphorylation, this protein recruits multiple adaptor proteins and downstream signaling molecules into multimolecular signaling complexes located near the site of TCR engagement. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":28984826,"end":28990783,"strand":1,"description":"linker for activation of T-cells [Source:HGNC Symbol;Acc:HGNC:18874]"}, {"versioned_ensembl_gene_id":"ENSG00000275163.1","gene_symbol":"AC117457.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":178419123,"end":178843300,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229589.1","gene_symbol":"ACVR2B-AS1","gene_name":"ACVR2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44161]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128640","summary":null,"start":38451027,"end":38454820,"strand":-1,"description":"ACVR2B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44161]"}, {"versioned_ensembl_gene_id":"ENSG00000274253.4","gene_symbol":"AC138649.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":22757857,"end":22778741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257507.1","gene_symbol":"LINC02373","gene_name":"long intergenic non-protein coding RNA 2373 [Source:HGNC Symbol;Acc:HGNC:53295]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369822","summary":null,"start":69449470,"end":69460724,"strand":1,"description":"long intergenic non-protein coding RNA 2373 [Source:HGNC Symbol;Acc:HGNC:53295]"}, {"versioned_ensembl_gene_id":"ENSG00000235689.1","gene_symbol":"AC253536.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24006305,"end":24008258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244362.3","gene_symbol":"KRTAP19-7","gene_name":"keratin associated protein 19-7 [Source:HGNC Symbol;Acc:HGNC:18942]","synonyms":"KAP19.7","biotype":"protein_coding","ncbi_id":"337974","summary":null,"start":30560875,"end":30561314,"strand":-1,"description":"keratin associated protein 19-7 [Source:HGNC Symbol;Acc:HGNC:18942]"}, {"versioned_ensembl_gene_id":"ENSG00000242036.1","gene_symbol":"AC128713.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167956311,"end":167956616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237149.5","gene_symbol":"ZNF503-AS2","gene_name":"ZNF503 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:23525]","synonyms":"NCRNA00245,C10orf41","biotype":"antisense_RNA","ncbi_id":"100131213","summary":null,"start":75401519,"end":75408982,"strand":1,"description":"ZNF503 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:23525]"}, {"versioned_ensembl_gene_id":"ENSG00000272880.1","gene_symbol":"AL161734.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181812705,"end":181813261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165714.10","gene_symbol":"BORCS5","gene_name":"BLOC-1 related complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:17950]","synonyms":"LOH1CR12,LOH12CR1","biotype":"protein_coding","ncbi_id":"118426","summary":null,"start":12357079,"end":12469694,"strand":1,"description":"BLOC-1 related complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:17950]"}, {"versioned_ensembl_gene_id":"ENSG00000087266.15","gene_symbol":"SH3BP2","gene_name":"SH3 domain binding protein 2 [Source:HGNC Symbol;Acc:HGNC:10825]","synonyms":"RES4-23,CRBM","biotype":"protein_coding","ncbi_id":"6452","summary":"The protein encoded by this gene has an N-terminal pleckstrin homology (PH) domain, an SH3-binding proline-rich region, and a C-terminal SH2 domain. The protein binds to the SH3 domains of several proteins including the ABL1 and SYK protein tyrosine kinases , and functions as a cytoplasmic adaptor protein to positively regulate transcriptional activity in T, natural killer (NK), and basophilic cells. Mutations in this gene result in cherubism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":2793023,"end":2841098,"strand":1,"description":"SH3 domain binding protein 2 [Source:HGNC Symbol;Acc:HGNC:10825]"}, {"versioned_ensembl_gene_id":"ENSG00000275016.4","gene_symbol":"AC015574.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95638346,"end":95825451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237436.1","gene_symbol":"AL590128.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6783892,"end":6784843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254209.1","gene_symbol":"AC104233.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121671773,"end":121684562,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240370.6","gene_symbol":"RPL13P5","gene_name":"ribosomal protein L13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30363]","synonyms":"RPL13L,RPL13-2","biotype":"transcribed_processed_pseudogene","ncbi_id":"283345","summary":null,"start":6873389,"end":6884741,"strand":1,"description":"ribosomal protein L13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30363]"}, {"versioned_ensembl_gene_id":"ENSG00000099875.14","gene_symbol":"MKNK2","gene_name":"MAP kinase interacting serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:7111]","synonyms":"MNK2,GPRK7","biotype":"protein_coding","ncbi_id":"2872","summary":"This gene encodes a member of the calcium/calmodulin-dependent protein kinases (CAMK) Ser/Thr protein kinase family, which belongs to the protein kinase superfamily. This protein contains conserved DLG (asp-leu-gly) and ENIL (glu-asn-ile-leu) motifs, and an N-terminal polybasic region which binds importin A and the translation factor scaffold protein eukaryotic initiation factor 4G (eIF4G). This protein is one of the downstream kinases activated by mitogen-activated protein (MAP) kinases. It phosphorylates the eukaryotic initiation factor 4E (eIF4E), thus playing important roles in the initiation of mRNA translation, oncogenic transformation and malignant cell proliferation. In addition to eIF4E, this protein also interacts with von Hippel-Lindau tumor suppressor (VHL), ring-box 1 (Rbx1) and Cullin2 (Cul2), which are all components of the CBC(VHL) ubiquitin ligase E3 complex. Multiple alternatively spliced transcript variants have been found, but the full-length nature and biological activity of only two variants are determined. These two variants encode distinct isoforms which differ in activity and regulation, and in subcellular localization. [provided by RefSeq, Aug 2011]","start":2037465,"end":2051244,"strand":-1,"description":"MAP kinase interacting serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:7111]"}, {"versioned_ensembl_gene_id":"ENSG00000253619.1","gene_symbol":"AC068413.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120913065,"end":121119754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240152.2","gene_symbol":"LINC02271","gene_name":"long intergenic non-protein coding RNA 2271 [Source:HGNC Symbol;Acc:HGNC:53186]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377249","summary":null,"start":61143656,"end":61153962,"strand":1,"description":"long intergenic non-protein coding RNA 2271 [Source:HGNC Symbol;Acc:HGNC:53186]"}, {"versioned_ensembl_gene_id":"ENSG00000244227.6","gene_symbol":"LRRC77P","gene_name":"leucine rich repeat containing 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:50536]","synonyms":"LINC01330","biotype":"transcribed_unitary_pseudogene","ncbi_id":"646168","summary":null,"start":167864773,"end":167924011,"strand":1,"description":"leucine rich repeat containing 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:50536]"}, {"versioned_ensembl_gene_id":"ENSG00000279995.1","gene_symbol":"AC139792.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34124162,"end":34124385,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169193.11","gene_symbol":"CCDC126","gene_name":"coiled-coil domain containing 126 [Source:HGNC Symbol;Acc:HGNC:22398]","synonyms":"FLJ23031","biotype":"protein_coding","ncbi_id":"90693","summary":null,"start":23597379,"end":23644708,"strand":1,"description":"coiled-coil domain containing 126 [Source:HGNC Symbol;Acc:HGNC:22398]"}, {"versioned_ensembl_gene_id":"ENSG00000100979.14","gene_symbol":"PLTP","gene_name":"phospholipid transfer protein [Source:HGNC Symbol;Acc:HGNC:9093]","synonyms":"BPIFE","biotype":"protein_coding","ncbi_id":"5360","summary":"The protein encoded by this gene is one of at least two lipid transfer proteins found in human plasma. The encoded protein transfers phospholipids from triglyceride-rich lipoproteins to high density lipoprotein (HDL). In addition to regulating the size of HDL particles, this protein may be involved in cholesterol metabolism. At least two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":45898621,"end":45912155,"strand":-1,"description":"phospholipid transfer protein [Source:HGNC Symbol;Acc:HGNC:9093]"}, {"versioned_ensembl_gene_id":"ENSG00000164600.6","gene_symbol":"NEUROD6","gene_name":"neuronal differentiation 6 [Source:HGNC Symbol;Acc:HGNC:13804]","synonyms":"NEX1M,Nex1,Math-2,bHLHa2,Atoh2","biotype":"protein_coding","ncbi_id":"63974","summary":"This gene is a member of the NEUROD family of basic helix-loop-helix transcription factors. The encoded protein may be involved in the development and differentiation of the nervous system. [provided by RefSeq, Nov 2012]","start":31337461,"end":31340894,"strand":-1,"description":"neuronal differentiation 6 [Source:HGNC Symbol;Acc:HGNC:13804]"}, {"versioned_ensembl_gene_id":"ENSG00000223976.1","gene_symbol":"EXTL2P1","gene_name":"exostosin like glycosyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3517]","synonyms":"EXTL2P","biotype":"processed_pseudogene","ncbi_id":"100287682","summary":null,"start":175842887,"end":175843302,"strand":1,"description":"exostosin like glycosyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3517]"}, {"versioned_ensembl_gene_id":"ENSG00000229066.1","gene_symbol":"AC093459.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175257250,"end":175454640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280012.2","gene_symbol":"RPL23AP61","gene_name":"ribosomal protein L23a pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:36016]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728484","summary":null,"start":46063250,"end":46063715,"strand":1,"description":"ribosomal protein L23a pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:36016]"}, {"versioned_ensembl_gene_id":"ENSG00000261436.5","gene_symbol":"AC018554.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60359842,"end":60442245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115020.16","gene_symbol":"PIKFYVE","gene_name":"phosphoinositide kinase, FYVE-type zinc finger containing [Source:HGNC Symbol;Acc:HGNC:23785]","synonyms":"ZFYVE29,PIP5K3,PIP5K,PIKfyve,p235,MGC40423,KIAA0981,FAB1","biotype":"protein_coding","ncbi_id":"200576","summary":"Phosphorylated derivatives of phosphatidylinositol (PtdIns) regulate cytoskeletal functions, membrane trafficking, and receptor signaling by recruiting protein complexes to cell- and endosomal-membranes. Humans have multiple PtdIns proteins that differ by the degree and position of phosphorylation of the inositol ring. This gene encodes an enzyme (PIKfyve; also known as phosphatidylinositol-3-phosphate 5-kinase type III or PIPKIII) that phosphorylates the D-5 position in PtdIns and phosphatidylinositol-3-phosphate (PtdIns3P) to make PtdIns5P and PtdIns(3,5)biphosphate. The D-5 position also can be phosphorylated by type I PtdIns4P-5-kinases (PIP5Ks) that are encoded by distinct genes and preferentially phosphorylate D-4 phosphorylated PtdIns. In contrast, PIKfyve preferentially phosphorylates D-3 phosphorylated PtdIns. In addition to being a lipid kinase, PIKfyve also has protein kinase activity. PIKfyve regulates endomembrane homeostasis and plays a role in the biogenesis of endosome carrier vesicles from early endosomes. Mutations in this gene cause corneal fleck dystrophy (CFD); an autosomal dominant disorder characterized by numerous small white flecks present in all layers of the corneal stroma. Histologically, these flecks appear to be keratocytes distended with lipid and mucopolysaccharide filled intracytoplasmic vacuoles. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]","start":208266267,"end":208358751,"strand":1,"description":"phosphoinositide kinase, FYVE-type zinc finger containing [Source:HGNC Symbol;Acc:HGNC:23785]"}, {"versioned_ensembl_gene_id":"ENSG00000261590.1","gene_symbol":"AC018554.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60357214,"end":60357474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080947.14","gene_symbol":"CROCCP3","gene_name":"ciliary rootlet coiled-coil, rootletin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29405]","synonyms":"KIAA1922,CROCCL2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"114819","summary":null,"start":16467436,"end":16499257,"strand":-1,"description":"ciliary rootlet coiled-coil, rootletin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29405]"}, {"versioned_ensembl_gene_id":"ENSG00000235002.1","gene_symbol":"AL513331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42412398,"end":42412794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189316.3","gene_symbol":"AC073349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64888527,"end":64890100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099984.11","gene_symbol":"GSTT2","gene_name":"glutathione S-transferase theta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4642]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"2953","summary":"The protein encoded by this gene, glutathione S-transferase (GST) theta 2 (GSTT2), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT2 and GSTT2B are nearly identical to each other, and share 55% amino acid identity with GSTT1. All three genes may play a role in human carcinogenesis. The GSTT2 gene is a pseudogene in some populations. [provided by RefSeq, Sep 2015]","start":23980058,"end":23983915,"strand":1,"description":"glutathione S-transferase theta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4642]"}, {"versioned_ensembl_gene_id":"ENSG00000272787.1","gene_symbol":"AC253536.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23969211,"end":23969873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232587.1","gene_symbol":"EEF1A1P3","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3194]","synonyms":"EEF1AL1,EEF1AL","biotype":"processed_pseudogene","ncbi_id":"100421865","summary":null,"start":28214513,"end":28215897,"strand":1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3194]"}, {"versioned_ensembl_gene_id":"ENSG00000232263.1","gene_symbol":"KRTAP25-1","gene_name":"keratin associated protein 25-1 [Source:HGNC Symbol;Acc:HGNC:34003]","synonyms":"KAP25.1","biotype":"protein_coding","ncbi_id":"100131902","summary":null,"start":30289145,"end":30289514,"strand":-1,"description":"keratin associated protein 25-1 [Source:HGNC Symbol;Acc:HGNC:34003]"}, {"versioned_ensembl_gene_id":"ENSG00000133433.10","gene_symbol":"GSTT2B","gene_name":"glutathione S-transferase theta 2B (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:33437]","synonyms":"GSTT2P","biotype":"protein_coding","ncbi_id":"653689","summary":"The protein encoded by this gene, glutathione S-transferase (GST) theta 2B (GSTT2B), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT2 and GSTT2B are nearly identical to each other, and share 55% amino acid identity with GSTT1. All three genes may play a role in human carcinogenesis. The GSTT2B gene is a pseudogene in some populations. [provided by RefSeq, Sep 2015]","start":23957414,"end":23961186,"strand":-1,"description":"glutathione S-transferase theta 2B (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:33437]"}, {"versioned_ensembl_gene_id":"ENSG00000242598.1","gene_symbol":"MED28P8","gene_name":"mediator complex subunit 28 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45085]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060144","summary":null,"start":81557121,"end":81557832,"strand":-1,"description":"mediator complex subunit 28 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:45085]"}, {"versioned_ensembl_gene_id":"ENSG00000197381.15","gene_symbol":"ADARB1","gene_name":"adenosine deaminase, RNA specific B1 [Source:HGNC Symbol;Acc:HGNC:226]","synonyms":"ADAR2b,ADAR2a-L3,ADAR2a-L2,ADAR2a-L1,ADAR2a,ADAR2,RED1,hRED1,DRADA2,DRABA2,ADAR2g,ADAR2d,ADAR2c","biotype":"protein_coding","ncbi_id":"104","summary":"This gene encodes the enzyme responsible for pre-mRNA editing of the glutamate receptor subunit B by site-specific deamination of adenosines. Studies in rat found that this enzyme acted on its own pre-mRNA molecules to convert an AA dinucleotide to an AI dinucleotide which resulted in a new splice site. Alternative splicing of this gene results in several transcript variants, some of which have been characterized by the presence or absence of an ALU cassette insert and a short or long C-terminal region. [provided by RefSeq, Jul 2008]","start":45073853,"end":45226560,"strand":1,"description":"adenosine deaminase, RNA specific B1 [Source:HGNC Symbol;Acc:HGNC:226]"}, {"versioned_ensembl_gene_id":"ENSG00000272666.1","gene_symbol":"U62317.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50542305,"end":50542906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163536.12","gene_symbol":"SERPINI1","gene_name":"serpin family I member 1 [Source:HGNC Symbol;Acc:HGNC:8943]","synonyms":"PI12,neuroserpin","biotype":"protein_coding","ncbi_id":"5274","summary":"This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":167735243,"end":167825568,"strand":1,"description":"serpin family I member 1 [Source:HGNC Symbol;Acc:HGNC:8943]"}, {"versioned_ensembl_gene_id":"ENSG00000189332.5","gene_symbol":"AC090099.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18209138,"end":18214562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262102.1","gene_symbol":"DSEL","gene_name":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]","synonyms":"FLJ11477,DE-epi2,C18orf4,NCAG1","biotype":"protein_coding","ncbi_id":"92126","summary":null,"start":67576031,"end":67586429,"strand":-1,"description":"dermatan sulfate epimerase-like [Source:HGNC Symbol;Acc:HGNC:18144]"}, {"versioned_ensembl_gene_id":"ENSG00000239432.1","gene_symbol":"AF186996.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125756086,"end":125756462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282112.1","gene_symbol":"AC110597.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67585995,"end":67586198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261200.1","gene_symbol":"AC136944.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33541842,"end":33545812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278848.2","gene_symbol":"TP53TG3F","gene_name":"TP53 target 3 family member F [Source:HGNC Symbol;Acc:HGNC:51817]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724127","summary":null,"start":33459045,"end":33462249,"strand":1,"description":"TP53 target 3 family member F [Source:HGNC Symbol;Acc:HGNC:51817]"}, {"versioned_ensembl_gene_id":"ENSG00000188582.8","gene_symbol":"PAQR9","gene_name":"progestin and adipoQ receptor family member 9 [Source:HGNC Symbol;Acc:HGNC:30131]","synonyms":"FLJ41938","biotype":"protein_coding","ncbi_id":"344838","summary":null,"start":142949164,"end":142963682,"strand":-1,"description":"progestin and adipoQ receptor family member 9 [Source:HGNC Symbol;Acc:HGNC:30131]"}, {"versioned_ensembl_gene_id":"ENSG00000261216.1","gene_symbol":"AC007216.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11908208,"end":11908916,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237900.2","gene_symbol":"ZBTB12","gene_name":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]","synonyms":"G10,D6S59E,C6orf46,NG35","biotype":"protein_coding","ncbi_id":"221527","summary":null,"start":31887151,"end":31889536,"strand":-1,"description":"zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:HGNC:19066]"}, {"versioned_ensembl_gene_id":"ENSG00000185182.14","gene_symbol":"GOLGA8DP","gene_name":"golgin A8 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32376]","synonyms":"GOLGA8D","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132979","summary":null,"start":22427039,"end":22437902,"strand":-1,"description":"golgin A8 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32376]"}, {"versioned_ensembl_gene_id":"ENSG00000273679.1","gene_symbol":"AC100757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22371736,"end":22373570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000061918.12","gene_symbol":"GUCY1B3","gene_name":"guanylate cyclase 1 soluble subunit beta [Source:HGNC Symbol;Acc:HGNC:4687]","synonyms":"GUC1B3,GC-SB3,GC-S-beta-1","biotype":"protein_coding","ncbi_id":"2983","summary":"This gene encodes the beta subunit of the soluble guanylate cyclase (sGC), which catalyzes the conversion of GTP (guanosine triphosphate) to cGMP (cyclic guanosine monophosphate). The encoded protein contains an HNOX domain, which serves as a receptor for ligands such as nitric oxide, oxygen and nitrovasodilator drugs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":155758992,"end":155807591,"strand":1,"description":"guanylate cyclase 1 soluble subunit beta [Source:HGNC Symbol;Acc:HGNC:4687]"}, {"versioned_ensembl_gene_id":"ENSG00000248533.1","gene_symbol":"AC034226.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37953402,"end":37966964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267647.1","gene_symbol":"AC098848.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54954403,"end":54954732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239783.1","gene_symbol":"AL121776.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47071865,"end":47072236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230634.1","gene_symbol":"AL031597.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46481329,"end":46481760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233313.2","gene_symbol":"HMGA1P5","gene_name":"high mobility group AT-hook 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19120]","synonyms":"HMGA1L5","biotype":"processed_pseudogene","ncbi_id":"387063","summary":null,"start":75276376,"end":75276646,"strand":-1,"description":"high mobility group AT-hook 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:19120]"}, {"versioned_ensembl_gene_id":"ENSG00000129235.10","gene_symbol":"TXNDC17","gene_name":"thioredoxin domain containing 17 [Source:HGNC Symbol;Acc:HGNC:28218]","synonyms":"TXNL5,TRP14,MGC14353","biotype":"protein_coding","ncbi_id":"84817","summary":null,"start":6640758,"end":6644541,"strand":1,"description":"thioredoxin domain containing 17 [Source:HGNC Symbol;Acc:HGNC:28218]"}, {"versioned_ensembl_gene_id":"ENSG00000278152.2","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"nkat5,183ActI,CD158J,cl-49","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738439,"end":54769215,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000226726.1","gene_symbol":"TMEM256P2","gene_name":"transmembrane protein 256 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45088]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479054","summary":null,"start":221532668,"end":221533008,"strand":1,"description":"transmembrane protein 256 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45088]"}, {"versioned_ensembl_gene_id":"ENSG00000249923.1","gene_symbol":"AC007663.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20198729,"end":20204918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263127.1","gene_symbol":"RPL4P5","gene_name":"ribosomal protein L4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"158345","summary":null,"start":7491857,"end":7493132,"strand":-1,"description":"ribosomal protein L4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35699]"}, {"versioned_ensembl_gene_id":"ENSG00000187446.11","gene_symbol":"CHP1","gene_name":"calcineurin like EF-hand protein 1 [Source:HGNC Symbol;Acc:HGNC:17433]","synonyms":"CHP,SLC9A1BP,Sid470p,p24,p22","biotype":"protein_coding","ncbi_id":"11261","summary":"This gene encodes a phosphoprotein that binds to the Na+/H+ exchanger NHE1. This protein serves as an essential cofactor which supports the physiological activity of NHE family members and may play a role in the mitogenic regulation of NHE1. The protein shares similarity with calcineurin B and calmodulin and it is also known to be an endogenous inhibitor of calcineurin activity. [provided by RefSeq, Jul 2008]","start":41230839,"end":41281890,"strand":1,"description":"calcineurin like EF-hand protein 1 [Source:HGNC Symbol;Acc:HGNC:17433]"}, {"versioned_ensembl_gene_id":"ENSG00000144802.11","gene_symbol":"NFKBIZ","gene_name":"NFKB inhibitor zeta [Source:HGNC Symbol;Acc:HGNC:29805]","synonyms":"MAIL,INAP,FLJ34463","biotype":"protein_coding","ncbi_id":"64332","summary":"This gene is a member of the ankyrin-repeat family and is induced by lipopolysaccharide (LPS). The C-terminal portion of the encoded product which contains the ankyrin repeats, shares high sequence similarity with the I kappa B family of proteins. The latter are known to play a role in inflammatory responses to LPS by their interaction with NF-B proteins through ankyrin-repeat domains. Studies in mouse indicate that this gene product is one of the nuclear I kappa B proteins and an activator of IL-6 production. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":101827991,"end":101861022,"strand":1,"description":"NFKB inhibitor zeta [Source:HGNC Symbol;Acc:HGNC:29805]"}, {"versioned_ensembl_gene_id":"ENSG00000248964.6","gene_symbol":"AC131254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29815004,"end":29854543,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280537.2","gene_symbol":"AC068946.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":219075329,"end":219170827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213599.10","gene_symbol":"SLX1A-SULT1A3","gene_name":"SLX1A-SULT1A3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44437]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100526830","summary":"This locus represents naturally occurring read-through transcription between the neighboring SLX1A (SLX1 structure-specific endonuclease subunit homolog A) and SULT1A3 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3) genes on the short arm of chromosome 16. A duplicate read-through locus also exists between the SLX1B and SULT1A4 genes located approximately 730 kb upstream on the same chromosome. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2017]","start":30193892,"end":30204310,"strand":1,"description":"SLX1A-SULT1A3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44437]"}, {"versioned_ensembl_gene_id":"ENSG00000277673.1","gene_symbol":"AL590808.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":106566021,"end":106566161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280190.1","gene_symbol":"AC027279.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78890231,"end":78892302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261599.6","gene_symbol":"HERC2P8","gene_name":"hect domain and RLD 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38747]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440366","summary":null,"start":33094204,"end":33129090,"strand":-1,"description":"hect domain and RLD 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38747]"}, {"versioned_ensembl_gene_id":"ENSG00000223985.1","gene_symbol":"LINC01874","gene_name":"long intergenic non-protein coding RNA 1874 [Source:HGNC Symbol;Acc:HGNC:52693]","synonyms":null,"biotype":"lincRNA","ncbi_id":"727944","summary":null,"start":490944,"end":492655,"strand":-1,"description":"long intergenic non-protein coding RNA 1874 [Source:HGNC Symbol;Acc:HGNC:52693]"}, {"versioned_ensembl_gene_id":"ENSG00000279670.1","gene_symbol":"AL359922.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21892188,"end":21893857,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264545.1","gene_symbol":"AL359922.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21802636,"end":22032986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218725.2","gene_symbol":"B3GALNT2P1","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51315]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130402","summary":null,"start":129800908,"end":129802214,"strand":1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51315]"}, {"versioned_ensembl_gene_id":"ENSG00000154479.12","gene_symbol":"CCDC173","gene_name":"coiled-coil domain containing 173 [Source:HGNC Symbol;Acc:HGNC:25064]","synonyms":"C2orf77,LOC129881","biotype":"protein_coding","ncbi_id":"129881","summary":null,"start":169645425,"end":169694433,"strand":-1,"description":"coiled-coil domain containing 173 [Source:HGNC Symbol;Acc:HGNC:25064]"}, {"versioned_ensembl_gene_id":"ENSG00000226072.1","gene_symbol":"AC016772.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169658132,"end":169661357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233836.7","gene_symbol":"AC139769.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23762944,"end":23833314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249579.2","gene_symbol":"AC113420.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63022919,"end":63023489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256220.1","gene_symbol":"AP003037.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61227168,"end":61248533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269378.1","gene_symbol":"AC022149.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14621634,"end":14622242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229298.1","gene_symbol":"TUBB8P1","gene_name":"tubulin beta 8 class VIII pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42182]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418937","summary":null,"start":21811621,"end":21812347,"strand":-1,"description":"tubulin beta 8 class VIII pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42182]"}, {"versioned_ensembl_gene_id":"ENSG00000147697.8","gene_symbol":"GSDMC","gene_name":"gasdermin C [Source:HGNC Symbol;Acc:HGNC:7151]","synonyms":"MLZE","biotype":"protein_coding","ncbi_id":"56169","summary":null,"start":129748196,"end":129786888,"strand":-1,"description":"gasdermin C [Source:HGNC Symbol;Acc:HGNC:7151]"}, {"versioned_ensembl_gene_id":"ENSG00000120907.17","gene_symbol":"ADRA1A","gene_name":"adrenoceptor alpha 1A [Source:HGNC Symbol;Acc:HGNC:277]","synonyms":"ADRA1C,ADRA1L1","biotype":"protein_coding","ncbi_id":"148","summary":"Alpha-1-adrenergic receptors (alpha-1-ARs) are members of the G protein-coupled receptor superfamily. They activate mitogenic responses and regulate growth and proliferation of many cells. There are 3 alpha-1-AR subtypes: alpha-1A, -1B and -1D, all of which signal through the Gq/11 family of G-proteins and different subtypes show different patterns of activation. This gene encodes alpha-1A-adrenergic receptor. Alternative splicing of this gene generates four transcript variants, which encode four different isoforms with distinct C-termini but having similar ligand binding properties. [provided by RefSeq, Jul 2008]","start":26748150,"end":26867273,"strand":-1,"description":"adrenoceptor alpha 1A [Source:HGNC Symbol;Acc:HGNC:277]"}, {"versioned_ensembl_gene_id":"ENSG00000276086.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724481,"end":54736671,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000249003.1","gene_symbol":"CLUHP4","gene_name":"clustered mitochondria homolog pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38470]","synonyms":"KIAA0664P4,KIAA0664L4","biotype":"unprocessed_pseudogene","ncbi_id":"100418711","summary":null,"start":190057902,"end":190063005,"strand":-1,"description":"clustered mitochondria homolog pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38470]"}, {"versioned_ensembl_gene_id":"ENSG00000250053.1","gene_symbol":"RARRES2P4","gene_name":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644881","summary":null,"start":190037916,"end":190038399,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]"}, {"versioned_ensembl_gene_id":"ENSG00000224265.1","gene_symbol":"AC068707.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43323665,"end":43327932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228048.1","gene_symbol":"AL355314.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55506219,"end":55513217,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231078.1","gene_symbol":"AL157414.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57105741,"end":57107128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067646.11","gene_symbol":"ZFY","gene_name":"zinc finger protein, Y-linked [Source:HGNC Symbol;Acc:HGNC:12870]","synonyms":"ZNF911","biotype":"protein_coding","ncbi_id":"7544","summary":"This gene encodes a zinc finger-containing protein that may function as a transcription factor. This gene was once a candidate gene for the testis-determining factor (TDF) and was erroneously referred to as TDF. [provided by RefSeq, Jul 2008]","start":2935281,"end":2982506,"strand":1,"description":"zinc finger protein, Y-linked [Source:HGNC Symbol;Acc:HGNC:12870]"}, {"versioned_ensembl_gene_id":"ENSG00000231604.2","gene_symbol":"AL133232.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56730397,"end":56731460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237000.1","gene_symbol":"PTMAP6","gene_name":"prothymosin, alpha pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16573]","synonyms":"dJ539E24.2","biotype":"processed_pseudogene","ncbi_id":"170542","summary":null,"start":56700837,"end":56701514,"strand":-1,"description":"prothymosin, alpha pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:16573]"}, {"versioned_ensembl_gene_id":"ENSG00000253535.5","gene_symbol":"AC120193.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24295814,"end":24912073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107742.12","gene_symbol":"SPOCK2","gene_name":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:13564]","synonyms":"testican-2,KIAA0275","biotype":"protein_coding","ncbi_id":"9806","summary":"This gene encodes a protein which binds with glycosaminoglycans to form part of the extracellular matrix. The protein contains thyroglobulin type-1, follistatin-like, and calcium-binding domains, and has glycosaminoglycan attachment sites in the acidic C-terminal region. Three alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":72059035,"end":72089032,"strand":-1,"description":"SPARC/osteonectin, cwcv and kazal like domains proteoglycan 2 [Source:HGNC Symbol;Acc:HGNC:13564]"}, {"versioned_ensembl_gene_id":"ENSG00000258088.1","gene_symbol":"AC078820.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75694010,"end":75698816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000020129.15","gene_symbol":"NCDN","gene_name":"neurochondrin [Source:HGNC Symbol;Acc:HGNC:17597]","synonyms":"NCDN-2,NCDN-1","biotype":"protein_coding","ncbi_id":"23154","summary":"This gene encodes a leucine-rich cytoplasmic protein, which is highly similar to a mouse protein that negatively regulates Ca/calmodulin-dependent protein kinase II phosphorylation and may be essential for spatial learning processes. Several alternatively spliced transcript variants of this gene have been described. [provided by RefSeq, Jul 2008]","start":35557473,"end":35567274,"strand":1,"description":"neurochondrin [Source:HGNC Symbol;Acc:HGNC:17597]"}, {"versioned_ensembl_gene_id":"ENSG00000123144.10","gene_symbol":"TRIR","gene_name":"telomerase RNA component interacting RNase [Source:HGNC Symbol;Acc:HGNC:28424]","synonyms":"TERCIR,MGC2803,fSAP18,C19orf43","biotype":"protein_coding","ncbi_id":"79002","summary":null,"start":12730640,"end":12734775,"strand":-1,"description":"telomerase RNA component interacting RNase [Source:HGNC Symbol;Acc:HGNC:28424]"}, {"versioned_ensembl_gene_id":"ENSG00000278847.1","gene_symbol":"AC006157.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2934406,"end":2934771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213361.2","gene_symbol":"AC004884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105244652,"end":105244970,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271482.1","gene_symbol":"AC005070.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105204600,"end":105204859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247213.6","gene_symbol":"LINC01498","gene_name":"long intergenic non-protein coding RNA 1498 [Source:HGNC Symbol;Acc:HGNC:51164]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723562","summary":null,"start":108434130,"end":108492585,"strand":-1,"description":"long intergenic non-protein coding RNA 1498 [Source:HGNC Symbol;Acc:HGNC:51164]"}, {"versioned_ensembl_gene_id":"ENSG00000272426.1","gene_symbol":"BX284668.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16904339,"end":16904776,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238142.1","gene_symbol":"BX284668.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16888538,"end":16889649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215589.3","gene_symbol":"KANK1P1","gene_name":"KN motif and ankyrin repeat domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52337]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862705","summary":null,"start":5928085,"end":5929318,"strand":-1,"description":"KN motif and ankyrin repeat domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52337]"}, {"versioned_ensembl_gene_id":"ENSG00000227790.7","gene_symbol":"AC015922.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15829369,"end":15908632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120949.14","gene_symbol":"TNFRSF8","gene_name":"TNF receptor superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:11923]","synonyms":"KI-1,D1S166E,CD30","biotype":"protein_coding","ncbi_id":"943","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed by activated, but not by resting, T and B cells. TRAF2 and TRAF5 can interact with this receptor, and mediate the signal transduction that leads to the activation of NF-kappaB. This receptor is a positive regulator of apoptosis, and also has been shown to limit the proliferative potential of autoreactive CD8 effector T cells and protect the body against autoimmunity. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":12063377,"end":12144207,"strand":1,"description":"TNF receptor superfamily member 8 [Source:HGNC Symbol;Acc:HGNC:11923]"}, {"versioned_ensembl_gene_id":"ENSG00000259545.2","gene_symbol":"AC013452.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49177610,"end":49178741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227408.1","gene_symbol":"AMYP1","gene_name":"amylase, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:479]","synonyms":"AMY2P","biotype":"unprocessed_pseudogene","ncbi_id":"281","summary":null,"start":103713723,"end":103719871,"strand":1,"description":"amylase, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:479]"}, {"versioned_ensembl_gene_id":"ENSG00000281429.1","gene_symbol":"FAM20C","gene_name":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]","synonyms":"IMAGE:4942737,G-CK,DMP4,DKFZp547D065","biotype":"protein_coding","ncbi_id":"56975","summary":"This gene encodes a member of the family of secreted protein kinases. The encoded protein binds calcium and phosphorylates proteins involved in bone mineralization. Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Apr 2014]","start":196274,"end":199037,"strand":1,"description":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]"}, {"versioned_ensembl_gene_id":"ENSG00000227062.2","gene_symbol":"AL596276.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":80464301,"end":80464718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000003400.14","gene_symbol":"CASP10","gene_name":"caspase 10 [Source:HGNC Symbol;Acc:HGNC:1500]","synonyms":"MCH4","biotype":"protein_coding","ncbi_id":"843","summary":"This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein cleaves and activates caspases 3 and 7, and the protein itself is processed by caspase 8. Mutations in this gene are associated with type IIA autoimmune lymphoproliferative syndrome, non-Hodgkin lymphoma and gastric cancer. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]","start":201182881,"end":201229406,"strand":1,"description":"caspase 10 [Source:HGNC Symbol;Acc:HGNC:1500]"}, {"versioned_ensembl_gene_id":"ENSG00000248921.1","gene_symbol":"AC021193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179856853,"end":179857581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259302.1","gene_symbol":"AC048382.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84505463,"end":84505495,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279271.1","gene_symbol":"AP006248.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17498647,"end":17499238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277397.1","gene_symbol":"AL606760.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":53180921,"end":53186900,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230852.1","gene_symbol":"AL161621.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84023055,"end":84024553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227339.1","gene_symbol":"THRAP3P1","gene_name":"thyroid hormone receptor associated protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32386]","synonyms":"THRAP3L","biotype":"processed_pseudogene","ncbi_id":"391524","summary":null,"start":31452832,"end":31455894,"strand":1,"description":"thyroid hormone receptor associated protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32386]"}, {"versioned_ensembl_gene_id":"ENSG00000215326.3","gene_symbol":"GPX1P2","gene_name":"glutathione peroxidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4561]","synonyms":"GPXP2,GPXL2,GPXL1,GPXP2P","biotype":"processed_pseudogene","ncbi_id":"2884","summary":null,"start":27143344,"end":27143949,"strand":-1,"description":"glutathione peroxidase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4561]"}, {"versioned_ensembl_gene_id":"ENSG00000214914.3","gene_symbol":"RPL23AP3","gene_name":"ribosomal protein L23a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10320]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"8489","summary":null,"start":36016079,"end":36016546,"strand":-1,"description":"ribosomal protein L23a pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10320]"}, {"versioned_ensembl_gene_id":"ENSG00000231106.2","gene_symbol":"LINC01436","gene_name":"long intergenic non-protein coding RNA 1436 [Source:HGNC Symbol;Acc:HGNC:50754]","synonyms":"AP000688.8","biotype":"lincRNA","ncbi_id":"100996609","summary":null,"start":36005338,"end":36007838,"strand":1,"description":"long intergenic non-protein coding RNA 1436 [Source:HGNC Symbol;Acc:HGNC:50754]"}, {"versioned_ensembl_gene_id":"ENSG00000232028.1","gene_symbol":"AC007391.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37325340,"end":37326797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230111.1","gene_symbol":"AC115283.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31269007,"end":31269406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253920.1","gene_symbol":"IGLV3-31","gene_name":"immunoglobulin lambda variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5913]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28788","summary":null,"start":22604445,"end":22605165,"strand":1,"description":"immunoglobulin lambda variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5913]"}, {"versioned_ensembl_gene_id":"ENSG00000274639.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736534,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284128.1","gene_symbol":"AP000356.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24644791,"end":24653356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261356.2","gene_symbol":"AC092368.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46571537,"end":46572136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264324.1","gene_symbol":"AC006030.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":74211604,"end":74363377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114391.12","gene_symbol":"RPL24","gene_name":"ribosomal protein L24 [Source:HGNC Symbol;Acc:HGNC:10325]","synonyms":"L24","biotype":"protein_coding","ncbi_id":"6152","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L24E family of ribosomal proteins. It is located in the cytoplasm. This gene has been referred to as ribosomal protein L30 because the encoded protein shares amino acid identity with the L30 ribosomal proteins from S. cerevisiae; however, its official name is ribosomal protein L24. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":101681091,"end":101686782,"strand":-1,"description":"ribosomal protein L24 [Source:HGNC Symbol;Acc:HGNC:10325]"}, {"versioned_ensembl_gene_id":"ENSG00000196472.4","gene_symbol":"AC111000.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69181660,"end":69182372,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232234.2","gene_symbol":"AL359378.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8329655,"end":8342455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282178.1","gene_symbol":"IGKV1OR10-1","gene_name":"immunoglobulin kappa variable 1/OR10-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44978]","synonyms":"IGKV1/OR10-1","biotype":"IG_V_pseudogene","ncbi_id":"642424","summary":null,"start":42186432,"end":42186884,"strand":1,"description":"immunoglobulin kappa variable 1/OR10-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44978]"}, {"versioned_ensembl_gene_id":"ENSG00000225141.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32124129,"end":32130145,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000186301.8","gene_symbol":"MST1P2","gene_name":"macrophage stimulating 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7383]","synonyms":"MSTP2,MSPL2,MSPL-2","biotype":"unprocessed_pseudogene","ncbi_id":"11209","summary":null,"start":16645622,"end":16650289,"strand":1,"description":"macrophage stimulating 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7383]"}, {"versioned_ensembl_gene_id":"ENSG00000231278.1","gene_symbol":"AC013469.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":240079433,"end":240080362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226476.3","gene_symbol":"LINC01748","gene_name":"long intergenic non-protein coding RNA 1748 [Source:HGNC Symbol;Acc:HGNC:52535]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378763","summary":null,"start":60515716,"end":60640491,"strand":-1,"description":"long intergenic non-protein coding RNA 1748 [Source:HGNC Symbol;Acc:HGNC:52535]"}, {"versioned_ensembl_gene_id":"ENSG00000011105.12","gene_symbol":"TSPAN9","gene_name":"tetraspanin 9 [Source:HGNC Symbol;Acc:HGNC:21640]","synonyms":"NET-5","biotype":"protein_coding","ncbi_id":"10867","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Nov 2009]","start":3077355,"end":3286564,"strand":1,"description":"tetraspanin 9 [Source:HGNC Symbol;Acc:HGNC:21640]"}, {"versioned_ensembl_gene_id":"ENSG00000282788.1","gene_symbol":"AC243791.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":15144760,"end":15175928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136238.17","gene_symbol":"RAC1","gene_name":"ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1) [Source:HGNC Symbol;Acc:HGNC:9801]","synonyms":"TC-25,Rac-1,p21-Rac1","biotype":"protein_coding","ncbi_id":"5879","summary":"The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":6374523,"end":6403977,"strand":1,"description":"ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1) [Source:HGNC Symbol;Acc:HGNC:9801]"}, {"versioned_ensembl_gene_id":"ENSG00000231073.1","gene_symbol":"AL590133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150973123,"end":150975534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237670.1","gene_symbol":"LINC01866","gene_name":"long intergenic non-protein coding RNA 1866 [Source:HGNC Symbol;Acc:HGNC:52685]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985806","summary":null,"start":16970034,"end":16974497,"strand":1,"description":"long intergenic non-protein coding RNA 1866 [Source:HGNC Symbol;Acc:HGNC:52685]"}, {"versioned_ensembl_gene_id":"ENSG00000277386.1","gene_symbol":"AL138999.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33336216,"end":33336716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283118.1","gene_symbol":"AC009951.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144444848,"end":144450450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203729.8","gene_symbol":"LINC00272","gene_name":"long intergenic non-protein coding RNA 272 [Source:HGNC Symbol;Acc:HGNC:26898]","synonyms":"C1orf120,RP1-223H12.3,NCRNA00272","biotype":"lincRNA","ncbi_id":"388719","summary":null,"start":182407621,"end":182414815,"strand":1,"description":"long intergenic non-protein coding RNA 272 [Source:HGNC Symbol;Acc:HGNC:26898]"}, {"versioned_ensembl_gene_id":"ENSG00000279152.1","gene_symbol":"AC129492.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8188933,"end":8189688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177200.16","gene_symbol":"CHD9","gene_name":"chromodomain helicase DNA binding protein 9 [Source:HGNC Symbol;Acc:HGNC:25701]","synonyms":"FLJ12178,BC022889,KIAA0308","biotype":"protein_coding","ncbi_id":"80205","summary":null,"start":53055033,"end":53329150,"strand":1,"description":"chromodomain helicase DNA binding protein 9 [Source:HGNC Symbol;Acc:HGNC:25701]"}, {"versioned_ensembl_gene_id":"ENSG00000203730.2","gene_symbol":"TEDDM1","gene_name":"transmembrane epididymal protein 1 [Source:HGNC Symbol;Acc:HGNC:30233]","synonyms":"TMEM45C,HE9,Epdd1,EDDM9","biotype":"protein_coding","ncbi_id":"127670","summary":null,"start":182398117,"end":182400616,"strand":-1,"description":"transmembrane epididymal protein 1 [Source:HGNC Symbol;Acc:HGNC:30233]"}, {"versioned_ensembl_gene_id":"ENSG00000226796.2","gene_symbol":"AL662826.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29570508,"end":29571435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236158.1","gene_symbol":"RFC3P1","gene_name":"replication factor C 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131711","summary":null,"start":36169767,"end":36170448,"strand":-1,"description":"replication factor C 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44531]"}, {"versioned_ensembl_gene_id":"ENSG00000224800.1","gene_symbol":"RPS27AP6","gene_name":"ribosomal protein S27a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36236]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271144","summary":null,"start":150881236,"end":150881683,"strand":-1,"description":"ribosomal protein S27a pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36236]"}, {"versioned_ensembl_gene_id":"ENSG00000101958.13","gene_symbol":"GLRA2","gene_name":"glycine receptor alpha 2 [Source:HGNC Symbol;Acc:HGNC:4327]","synonyms":"GLR","biotype":"protein_coding","ncbi_id":"2742","summary":"The glycine receptor consists of two subunits, alpha and beta, and acts as a pentamer. The protein encoded by this gene is an alpha subunit and can bind strychnine. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]","start":14529298,"end":14731812,"strand":1,"description":"glycine receptor alpha 2 [Source:HGNC Symbol;Acc:HGNC:4327]"}, {"versioned_ensembl_gene_id":"ENSG00000261468.1","gene_symbol":"AC096921.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":30697661,"end":30699576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275565.4","gene_symbol":"ALOX5","gene_name":"arachidonate 5-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:435]","synonyms":"5-LOX","biotype":"protein_coding","ncbi_id":"240","summary":"This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":45390239,"end":45462182,"strand":1,"description":"arachidonate 5-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:435]"}, {"versioned_ensembl_gene_id":"ENSG00000263057.2","gene_symbol":"KRT20","gene_name":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]","synonyms":"K20,CK20,MGC35423","biotype":"protein_coding","ncbi_id":"54474","summary":"The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This cytokeratin is a major cellular protein of mature enterocytes and goblet cells and is specifically expressed in the gastric and intestinal mucosa. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2008]","start":40875941,"end":40885227,"strand":-1,"description":"keratin 20 [Source:HGNC Symbol;Acc:HGNC:20412]"}, {"versioned_ensembl_gene_id":"ENSG00000154451.14","gene_symbol":"GBP5","gene_name":"guanylate binding protein 5 [Source:HGNC Symbol;Acc:HGNC:19895]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115362","summary":"This gene belongs to the TRAFAC class dynamin-like GTPase superfamily. The encoded protein acts as an activator of NLRP3 inflammasome assembly and has a role in innate immunity and inflammation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2017]","start":89258950,"end":89272804,"strand":-1,"description":"guanylate binding protein 5 [Source:HGNC Symbol;Acc:HGNC:19895]"}, {"versioned_ensembl_gene_id":"ENSG00000236754.5","gene_symbol":"AC007666.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17580157,"end":17589192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005108.15","gene_symbol":"THSD7A","gene_name":"thrombospondin type 1 domain containing 7A [Source:HGNC Symbol;Acc:HGNC:22207]","synonyms":"KIAA0960","biotype":"protein_coding","ncbi_id":"221981","summary":"The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]","start":11370357,"end":11832198,"strand":-1,"description":"thrombospondin type 1 domain containing 7A [Source:HGNC Symbol;Acc:HGNC:22207]"}, {"versioned_ensembl_gene_id":"ENSG00000103966.10","gene_symbol":"EHD4","gene_name":"EH domain containing 4 [Source:HGNC Symbol;Acc:HGNC:3245]","synonyms":"PAST4","biotype":"protein_coding","ncbi_id":"30844","summary":null,"start":41895939,"end":41972578,"strand":-1,"description":"EH domain containing 4 [Source:HGNC Symbol;Acc:HGNC:3245]"}, {"versioned_ensembl_gene_id":"ENSG00000278128.1","gene_symbol":"AL139093.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23854444,"end":23855457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235089.1","gene_symbol":"AL357632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81208568,"end":81209210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229752.1","gene_symbol":"RPL7P10","gene_name":"ribosomal protein L7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36599]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646538","summary":null,"start":81098267,"end":81099005,"strand":-1,"description":"ribosomal protein L7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36599]"}, {"versioned_ensembl_gene_id":"ENSG00000225710.1","gene_symbol":"AL355149.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16548651,"end":16552531,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163811.11","gene_symbol":"WDR43","gene_name":"WD repeat domain 43 [Source:HGNC Symbol;Acc:HGNC:28945]","synonyms":"UTP5,NET12,KIAA0007","biotype":"protein_coding","ncbi_id":"23160","summary":null,"start":28894643,"end":28948222,"strand":1,"description":"WD repeat domain 43 [Source:HGNC Symbol;Acc:HGNC:28945]"}, {"versioned_ensembl_gene_id":"ENSG00000257896.1","gene_symbol":"AC093012.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43736628,"end":43741067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132406.11","gene_symbol":"TMEM128","gene_name":"transmembrane protein 128 [Source:HGNC Symbol;Acc:HGNC:28201]","synonyms":"MGC13159","biotype":"protein_coding","ncbi_id":"85013","summary":null,"start":4235542,"end":4248212,"strand":-1,"description":"transmembrane protein 128 [Source:HGNC Symbol;Acc:HGNC:28201]"}, {"versioned_ensembl_gene_id":"ENSG00000282080.1","gene_symbol":"AC006511.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8014093,"end":8019007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163982.5","gene_symbol":"OTOP1","gene_name":"otopetrin 1 [Source:HGNC Symbol;Acc:HGNC:19656]","synonyms":null,"biotype":"protein_coding","ncbi_id":"133060","summary":"This gene encodes a transmembrane protein which belongs to the otopetrin domain protein family and is required for the formation of otoconia and otoliths, calcium carbonate biominerals within the inner ear of mammals that are required for the detection of linear acceleration and gravity. This gene modulates purinergic control of intracellular calcium in vestibular supporting cells. Naturally occurring mutations in the orthologous mouse gene are associated with nonsyndromic otoconia agenesis and a consequent balance defect. The orthologous mouse gene is also induced in white adipose tissue during obesity. The encoded protein is a component of a counterinflammatory pathway that attenuates obesity-induced adipose tissue inflammation and plays an adaptive role in maintaining metabolic homeostasis in obesity. [provided by RefSeq, Jul 2017]","start":4188803,"end":4226889,"strand":-1,"description":"otopetrin 1 [Source:HGNC Symbol;Acc:HGNC:19656]"}, {"versioned_ensembl_gene_id":"ENSG00000164237.8","gene_symbol":"CMBL","gene_name":"carboxymethylenebutenolidase homolog [Source:HGNC Symbol;Acc:HGNC:25090]","synonyms":"FLJ23617","biotype":"protein_coding","ncbi_id":"134147","summary":"CMBL (EC 3.1.1.45) is a cysteine hydrolase of the dienelactone hydrolase family that is highly expressed in liver cytosol. CMBL preferentially cleaves cyclic esters, and it activates medoxomil-ester prodrugs in which the medoxomil moiety is linked to an oxygen atom (Ishizuka et al., 2010 [PubMed 20177059]).[supplied by OMIM, Apr 2010]","start":10275875,"end":10308026,"strand":-1,"description":"carboxymethylenebutenolidase homolog [Source:HGNC Symbol;Acc:HGNC:25090]"}, {"versioned_ensembl_gene_id":"ENSG00000203356.2","gene_symbol":"LINC01562","gene_name":"long intergenic non-protein coding RNA 1562 [Source:HGNC Symbol;Acc:HGNC:51335]","synonyms":"RP11-296A18.3","biotype":"lincRNA","ncbi_id":"105378716","summary":null,"start":51195095,"end":51235096,"strand":-1,"description":"long intergenic non-protein coding RNA 1562 [Source:HGNC Symbol;Acc:HGNC:51335]"}, {"versioned_ensembl_gene_id":"ENSG00000271715.1","gene_symbol":"AC012640.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10269489,"end":10269918,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000002330.13","gene_symbol":"BAD","gene_name":"BCL2 associated agonist of cell death [Source:HGNC Symbol;Acc:HGNC:936]","synonyms":"BCL2L8,BBC2","biotype":"protein_coding","ncbi_id":"572","summary":"The protein encoded by this gene is a member of the BCL-2 family. BCL-2 family members are known to be regulators of programmed cell death. This protein positively regulates cell apoptosis by forming heterodimers with BCL-xL (B-cell lymphoma-extra large) and BCL-2, and reversing their death repressor activity. Proapoptotic activity of this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the regulation of this protein. Alternative splicing of this gene results in two transcript variants which encode the same isoform. [provided by RefSeq, Dec 2019]","start":64269830,"end":64284704,"strand":-1,"description":"BCL2 associated agonist of cell death [Source:HGNC Symbol;Acc:HGNC:936]"}, {"versioned_ensembl_gene_id":"ENSG00000179580.9","gene_symbol":"RNF151","gene_name":"ring finger protein 151 [Source:HGNC Symbol;Acc:HGNC:23235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146310","summary":null,"start":1966823,"end":1968975,"strand":1,"description":"ring finger protein 151 [Source:HGNC Symbol;Acc:HGNC:23235]"}, {"versioned_ensembl_gene_id":"ENSG00000273889.2","gene_symbol":"FAM83H","gene_name":"family with sequence similarity 83 member H [Source:HGNC Symbol;Acc:HGNC:24797]","synonyms":"FLJ46072","biotype":"protein_coding","ncbi_id":"286077","summary":"The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010]","start":143710940,"end":143720808,"strand":-1,"description":"family with sequence similarity 83 member H [Source:HGNC Symbol;Acc:HGNC:24797]"}, {"versioned_ensembl_gene_id":"ENSG00000282721.1","gene_symbol":"AC069363.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36073222,"end":36090476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262380.1","gene_symbol":"AC026401.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":15683290,"end":15684570,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230708.10","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":32997896,"end":33009106,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000180481.10","gene_symbol":"GLIPR1L2","gene_name":"GLI pathogenesis related 1 like 2 [Source:HGNC Symbol;Acc:HGNC:28592]","synonyms":"MGC39497","biotype":"protein_coding","ncbi_id":"144321","summary":"This gene encodes a member of the cysteine-rich secretory protein, antigen 5, and pathogenesis-related 1 superfamily. Members of this family have roles in a variety of processes, including cancer and immune defense. This gene is located in a cluster with two related genes on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":75391070,"end":75432688,"strand":1,"description":"GLI pathogenesis related 1 like 2 [Source:HGNC Symbol;Acc:HGNC:28592]"}, {"versioned_ensembl_gene_id":"ENSG00000274221.2","gene_symbol":"CCL3","gene_name":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]","synonyms":"SCYA3,MIP-1-alpha,LD78ALPHA,G0S19-1","biotype":"protein_coding","ncbi_id":"6348","summary":"This locus represents a small inducible cytokine. The encoded protein, also known as macrophage inflammatory protein 1 alpha, plays a role in inflammatory responses through binding to the receptors CCR1, CCR4 and CCR5. Polymorphisms at this locus may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1.[provided by RefSeq, Sep 2010]","start":36088598,"end":36090511,"strand":-1,"description":"C-C motif chemokine ligand 3 [Source:HGNC Symbol;Acc:HGNC:10627]"}, {"versioned_ensembl_gene_id":"ENSG00000163499.11","gene_symbol":"CRYBA2","gene_name":"crystallin beta A2 [Source:HGNC Symbol;Acc:HGNC:2395]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1412","summary":"Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of the vertebrate eye, which function to maintain the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also defined as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group but absent in the acidic group). Beta-crystallins form aggregates of different sizes and are able to form homodimers through self-association or heterodimers with other beta-crystallins. This gene is a beta acidic group member. Three alternatively spliced transcript variants encoding identical proteins have been reported. [provided by RefSeq, Jul 2008]","start":218990189,"end":218993421,"strand":-1,"description":"crystallin beta A2 [Source:HGNC Symbol;Acc:HGNC:2395]"}, {"versioned_ensembl_gene_id":"ENSG00000237840.6","gene_symbol":"FAM21FP","gene_name":"family with sequence similarity 21 member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:45011]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288690","summary":null,"start":45706431,"end":45727231,"strand":-1,"description":"family with sequence similarity 21 member F, pseudogene [Source:HGNC Symbol;Acc:HGNC:45011]"}, {"versioned_ensembl_gene_id":"ENSG00000134871.17","gene_symbol":"COL4A2","gene_name":"collagen type IV alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2203]","synonyms":"FLJ22259,DKFZp686I14213","biotype":"protein_coding","ncbi_id":"1284","summary":"This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. The C-terminal portion of the protein, known as canstatin, is an inhibitor of angiogenesis and tumor growth. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. [provided by RefSeq, Jul 2008]","start":110305812,"end":110513027,"strand":1,"description":"collagen type IV alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2203]"}, {"versioned_ensembl_gene_id":"ENSG00000188674.10","gene_symbol":"C2orf80","gene_name":"chromosome 2 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:34352]","synonyms":"LOC389073,GONDA1","biotype":"protein_coding","ncbi_id":"389073","summary":null,"start":208165343,"end":208190073,"strand":-1,"description":"chromosome 2 open reading frame 80 [Source:HGNC Symbol;Acc:HGNC:34352]"}, {"versioned_ensembl_gene_id":"ENSG00000060237.16","gene_symbol":"WNK1","gene_name":"WNK lysine deficient protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:14540]","synonyms":"PRKWNK1,PPP1R167,HSN2,HSAN2","biotype":"protein_coding","ncbi_id":"65125","summary":"This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]","start":752593,"end":911452,"strand":1,"description":"WNK lysine deficient protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:14540]"}, {"versioned_ensembl_gene_id":"ENSG00000075213.10","gene_symbol":"SEMA3A","gene_name":"semaphorin 3A [Source:HGNC Symbol;Acc:HGNC:10723]","synonyms":"SemD,SEMAD,SEMA1,Hsema-I,coll-1","biotype":"protein_coding","ncbi_id":"10371","summary":"This gene is a member of the semaphorin family and encodes a protein with an Ig-like C2-type (immunoglobulin-like) domain, a PSI domain and a Sema domain. This secreted protein can function as either a chemorepulsive agent, inhibiting axonal outgrowth, or as a chemoattractive agent, stimulating the growth of apical dendrites. In both cases, the protein is vital for normal neuronal pattern development. Increased expression of this protein is associated with schizophrenia and is seen in a variety of human tumor cell lines. Also, aberrant release of this protein is associated with the progression of Alzheimer's disease. [provided by RefSeq, Jul 2008]","start":83955777,"end":84492724,"strand":-1,"description":"semaphorin 3A [Source:HGNC Symbol;Acc:HGNC:10723]"}, {"versioned_ensembl_gene_id":"ENSG00000267004.1","gene_symbol":"AC018761.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12725517,"end":12725886,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268789.1","gene_symbol":"VN1R87P","gene_name":"vomeronasal 1 receptor 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:37407]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312832","summary":null,"start":22742924,"end":22743410,"strand":-1,"description":"vomeronasal 1 receptor 87 pseudogene [Source:HGNC Symbol;Acc:HGNC:37407]"}, {"versioned_ensembl_gene_id":"ENSG00000253488.1","gene_symbol":"FAM60DP","gene_name":"family with sequence similarity 60 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:19896]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646721","summary":null,"start":23634876,"end":23635507,"strand":-1,"description":"family with sequence similarity 60 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:19896]"}, {"versioned_ensembl_gene_id":"ENSG00000123569.8","gene_symbol":"H2BFWT","gene_name":"H2B histone family member W, testis specific [Source:HGNC Symbol;Acc:HGNC:27252]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158983","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the H2B histone family that is specifically expressed in sperm nuclei. A polymorphism in the 5' UTR of this gene is associated with male infertility.[provided by RefSeq, Oct 2015]","start":104011147,"end":104013687,"strand":-1,"description":"H2B histone family member W, testis specific [Source:HGNC Symbol;Acc:HGNC:27252]"}, {"versioned_ensembl_gene_id":"ENSG00000213918.10","gene_symbol":"DNASE1","gene_name":"deoxyribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:2956]","synonyms":"DNL1","biotype":"protein_coding","ncbi_id":"1773","summary":"This gene encodes a member of the DNase family. This protein is stored in the zymogen granules of the nuclear envelope and functions by cleaving DNA in an endonucleolytic manner. At least six autosomal codominant alleles have been characterized, DNASE1*1 through DNASE1*6, and the sequence of DNASE1*2 represented in this record. Mutations in this gene have been associated with systemic lupus erythematosus (SLE), an autoimmune disease. A recombinant form of this protein is used to treat the one of the symptoms of cystic fibrosis by hydrolyzing the extracellular DNA in sputum and reducing its viscosity. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":3611728,"end":3680143,"strand":1,"description":"deoxyribonuclease 1 [Source:HGNC Symbol;Acc:HGNC:2956]"}, {"versioned_ensembl_gene_id":"ENSG00000204560.9","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DBP2,Prp2,DDX16,PRPF2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30653119,"end":30673037,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000276754.1","gene_symbol":"AC006111.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3686998,"end":3687380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232652.1","gene_symbol":"AL662869.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29494080,"end":29507127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266900.1","gene_symbol":"AC027514.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":62245810,"end":62247412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255288.1","gene_symbol":"AL358944.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30167163,"end":30167306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282228.1","gene_symbol":"PAM16","gene_name":"presequence translocase associated motor 16 homolog [Source:HGNC Symbol;Acc:HGNC:29679]","synonyms":"TIMM16,Tim16,Magmas","biotype":"protein_coding","ncbi_id":"51025","summary":"This gene encodes a mitochondrial protein involved in granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling. This protein also plays a role in the import of nuclear-encoded mitochondrial proteins into the mitochondrial matrix and may be important in reactive oxygen species (ROS) homeostasis. Mutations in this gene cause Megarbane-Dagher-Melike type spondylometaphyseal dysplasia, an early lethal skeletal dysplasia characterized by short stature, developmental delay and other skeletal abnormalities. [provided by RefSeq, May 2017]","start":4331549,"end":4356579,"strand":-1,"description":"presequence translocase associated motor 16 homolog [Source:HGNC Symbol;Acc:HGNC:29679]"}, {"versioned_ensembl_gene_id":"ENSG00000229875.1","gene_symbol":"EIF1P1","gene_name":"eukaryotic translation initiation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49614]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505855","summary":null,"start":659986,"end":660326,"strand":1,"description":"eukaryotic translation initiation factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49614]"}, {"versioned_ensembl_gene_id":"ENSG00000242908.6","gene_symbol":"AADACL2-AS1","gene_name":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928142","summary":null,"start":151751443,"end":151928175,"strand":-1,"description":"AADACL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50301]"}, {"versioned_ensembl_gene_id":"ENSG00000185008.17","gene_symbol":"ROBO2","gene_name":"roundabout guidance receptor 2 [Source:HGNC Symbol;Acc:HGNC:10250]","synonyms":"KIAA1568","biotype":"protein_coding","ncbi_id":"6092","summary":"The protein encoded by this gene belongs to the ROBO family, part of the immunoglobulin superfamily of proteins that are highly conserved from fly to human. The encoded protein is a transmembrane receptor for the slit homolog 2 protein and functions in axon guidance and cell migration. Mutations in this gene are associated with vesicoureteral reflux, characterized by the backward flow of urine from the bladder into the ureters or the kidney. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":75906695,"end":77649964,"strand":1,"description":"roundabout guidance receptor 2 [Source:HGNC Symbol;Acc:HGNC:10250]"}, {"versioned_ensembl_gene_id":"ENSG00000274205.4","gene_symbol":"MAPK15","gene_name":"mitogen-activated protein kinase 15 [Source:HGNC Symbol;Acc:HGNC:24667]","synonyms":"ERK8,ERK7","biotype":"protein_coding","ncbi_id":"225689","summary":null,"start":143703266,"end":143709465,"strand":1,"description":"mitogen-activated protein kinase 15 [Source:HGNC Symbol;Acc:HGNC:24667]"}, {"versioned_ensembl_gene_id":"ENSG00000230978.1","gene_symbol":"LINC00160","gene_name":"long intergenic non-protein coding RNA 160 [Source:HGNC Symbol;Acc:HGNC:1294]","synonyms":"NCRNA00160,C21orf52","biotype":"lincRNA","ncbi_id":"54064","summary":null,"start":34723807,"end":34737181,"strand":-1,"description":"long intergenic non-protein coding RNA 160 [Source:HGNC Symbol;Acc:HGNC:1294]"}, {"versioned_ensembl_gene_id":"ENSG00000257654.1","gene_symbol":"AC125603.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116698336,"end":116703130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237317.2","gene_symbol":"AL022400.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174367105,"end":174368039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278823.4","gene_symbol":"C16orf45","gene_name":"chromosome 16 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:19213]","synonyms":"FLJ32618","biotype":"protein_coding","ncbi_id":"89927","summary":null,"start":15519415,"end":15710184,"strand":1,"description":"chromosome 16 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:19213]"}, {"versioned_ensembl_gene_id":"ENSG00000258457.5","gene_symbol":"AL132780.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22982698,"end":22999078,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137076.20","gene_symbol":"TLN1","gene_name":"talin 1 [Source:HGNC Symbol;Acc:HGNC:11845]","synonyms":"TLN,ILWEQ","biotype":"protein_coding","ncbi_id":"7094","summary":"This gene encodes a cytoskeletal protein that is concentrated in areas of cell-substratum and cell-cell contacts. The encoded protein plays a significant role in the assembly of actin filaments and in spreading and migration of various cell types, including fibroblasts and osteoclasts. It codistributes with integrins in the cell surface membrane in order to assist in the attachment of adherent cells to extracellular matrices and of lymphocytes to other cells. The N-terminus of this protein contains elements for localization to cell-extracellular matrix junctions. The C-terminus contains binding sites for proteins such as beta-1-integrin, actin, and vinculin. [provided by RefSeq, Feb 2009]","start":35696948,"end":35732395,"strand":-1,"description":"talin 1 [Source:HGNC Symbol;Acc:HGNC:11845]"}, {"versioned_ensembl_gene_id":"ENSG00000280129.1","gene_symbol":"AL132780.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23005499,"end":23007123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280387.1","gene_symbol":"AL109806.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56522252,"end":56523499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158411.11","gene_symbol":"MITD1","gene_name":"microtubule interacting and trafficking domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25207]","synonyms":"LOC129531","biotype":"protein_coding","ncbi_id":"129531","summary":"Abscission, the separation of daughter cells at the end of cytokinesis, is effected by endosomal sorting complexes required for transport III (ESCRT-III). The protein encoded by this gene functions as a homodimer, with the N-termini binding to a subset of ESCRT-III subunits and the C-termini binding to membranes. The encoded protein regulates ESCRT-III activity and is required for proper cytokinesis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":99161427,"end":99181058,"strand":-1,"description":"microtubule interacting and trafficking domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25207]"}, {"versioned_ensembl_gene_id":"ENSG00000255047.1","gene_symbol":"HNRNPRP2","gene_name":"heterogeneous nuclear ribonucleoprotein R pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44908]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421354","summary":null,"start":29668886,"end":29669628,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein R pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44908]"}, {"versioned_ensembl_gene_id":"ENSG00000144182.16","gene_symbol":"LIPT1","gene_name":"lipoyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:29569]","synonyms":"MGC13378,MGC12290","biotype":"protein_coding","ncbi_id":"51601","summary":"The process of transferring lipoic acid to proteins is a two-step process. The first step is the activation of lipoic acid by lipoate-activating enzyme to form lipoyl-AMP. For the second step, the protein encoded by this gene transfers the lipoyl moiety to apoproteins. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 13. Read-through transcription also exists between this gene and the neighboring downstream mitochondrial ribosomal protein L30 (MRPL30) gene. [provided by RefSeq, Mar 2011]","start":99154955,"end":99163157,"strand":1,"description":"lipoyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:29569]"}, {"versioned_ensembl_gene_id":"ENSG00000125900.12","gene_symbol":"SIRPD","gene_name":"signal regulatory protein delta [Source:HGNC Symbol;Acc:HGNC:16248]","synonyms":"PTPNS1L2,dJ576H24.4","biotype":"protein_coding","ncbi_id":"128646","summary":null,"start":1534251,"end":1558843,"strand":-1,"description":"signal regulatory protein delta [Source:HGNC Symbol;Acc:HGNC:16248]"}, {"versioned_ensembl_gene_id":"ENSG00000129128.12","gene_symbol":"SPCS3","gene_name":"signal peptidase complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26212]","synonyms":"YLR066W,SPC3,SPC22/23,PRO3567,FLJ22649","biotype":"protein_coding","ncbi_id":"60559","summary":null,"start":176319964,"end":176332245,"strand":1,"description":"signal peptidase complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26212]"}, {"versioned_ensembl_gene_id":"ENSG00000126602.10","gene_symbol":"TRAP1","gene_name":"TNF receptor associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16264]","synonyms":"HSP90L,HSP75","biotype":"protein_coding","ncbi_id":"10131","summary":"This gene encodes a mitochondrial chaperone protein that is member of the heat shock protein 90 (HSP90) family. The encoded protein has ATPase activity and interacts with tumor necrosis factor type I. This protein may function in regulating cellular stress responses. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":3651639,"end":3717597,"strand":-1,"description":"TNF receptor associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16264]"}, {"versioned_ensembl_gene_id":"ENSG00000248990.1","gene_symbol":"AC100773.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28679183,"end":28683469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115252.18","gene_symbol":"PDE1A","gene_name":"phosphodiesterase 1A [Source:HGNC Symbol;Acc:HGNC:8774]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5136","summary":"Cyclic nucleotide phosphodiesterases (PDEs) play a role in signal transduction by regulating intracellular cyclic nucleotide concentrations through hydrolysis of cAMP and/or cGMP to their respective nucleoside 5-prime monophosphates. Members of the PDE1 family, such as PDE1A, are Ca(2+)/calmodulin (see CALM1; MIM 114180)-dependent PDEs (CaM-PDEs) that are activated by calmodulin in the presence of Ca(2+) (Michibata et al., 2001 [PubMed 11342109]; Fidock et al., 2002 [PubMed 11747989]).[supplied by OMIM, Oct 2009]","start":182140036,"end":182523192,"strand":-1,"description":"phosphodiesterase 1A [Source:HGNC Symbol;Acc:HGNC:8774]"}, {"versioned_ensembl_gene_id":"ENSG00000223362.1","gene_symbol":"CDY15P","gene_name":"chromodomain Y-linked 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:23859]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386737","summary":null,"start":23855522,"end":23857091,"strand":-1,"description":"chromodomain Y-linked 15 pseudogene [Source:HGNC Symbol;Acc:HGNC:23859]"}, {"versioned_ensembl_gene_id":"ENSG00000188100.8","gene_symbol":"FAM25A","gene_name":"family with sequence similarity 25 member A [Source:HGNC Symbol;Acc:HGNC:23436]","synonyms":"bA96C23.5","biotype":"protein_coding","ncbi_id":"643161","summary":null,"start":87020306,"end":87024730,"strand":1,"description":"family with sequence similarity 25 member A [Source:HGNC Symbol;Acc:HGNC:23436]"}, {"versioned_ensembl_gene_id":"ENSG00000237302.1","gene_symbol":"OFD1P11Y","gene_name":"OFD1 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:23883]","synonyms":"OFDYP11,OFD1PY11,OFD1P11","biotype":"unprocessed_pseudogene","ncbi_id":"386695","summary":null,"start":23771232,"end":23798150,"strand":1,"description":"OFD1 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:23883]"}, {"versioned_ensembl_gene_id":"ENSG00000256837.1","gene_symbol":"CACNA1C-IT1","gene_name":"CACNA1C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41312]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"107984540","summary":null,"start":2018213,"end":2020532,"strand":1,"description":"CACNA1C intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41312]"}, {"versioned_ensembl_gene_id":"ENSG00000261569.5","gene_symbol":"AC138907.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32649193,"end":32663956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266990.1","gene_symbol":"AC004528.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":999796,"end":1002757,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164122.8","gene_symbol":"ASB5","gene_name":"ankyrin repeat and SOCS box containing 5 [Source:HGNC Symbol;Acc:HGNC:17180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140458","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Multiple alternatively spliced transcript variants have been described for this gene but their full length sequences are not known. [provided by RefSeq, Jul 2008]","start":176213673,"end":176277571,"strand":-1,"description":"ankyrin repeat and SOCS box containing 5 [Source:HGNC Symbol;Acc:HGNC:17180]"}, {"versioned_ensembl_gene_id":"ENSG00000259694.1","gene_symbol":"AC136698.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84171178,"end":84173194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236513.1","gene_symbol":"AC074035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4627200,"end":4633572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280038.1","gene_symbol":"DNM1P41","gene_name":"dynamin 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35191]","synonyms":"DNM1DN11@,DNM1DN11-6","biotype":"TEC","ncbi_id":"440299","summary":null,"start":84166547,"end":84169896,"strand":-1,"description":"dynamin 1 pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35191]"}, {"versioned_ensembl_gene_id":"ENSG00000261822.1","gene_symbol":"AC018362.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42567031,"end":42569994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106608.16","gene_symbol":"URGCP","gene_name":"upregulator of cell proliferation [Source:HGNC Symbol;Acc:HGNC:30890]","synonyms":"URG4,FLJ20654,KIAA1507,DKFZp686O0457,DKFZp666G166","biotype":"protein_coding","ncbi_id":"55665","summary":"URG4 is upregulated in the presence of hepatitis B virus (HBV)-encoded X antigen (HBxAg) and may contribute to the development of hepatocellular carcinoma by promoting hepatocellular growth and survival (Tufan et al., 2002 [PubMed 12082552]).[supplied by OMIM, Mar 2008]","start":43875894,"end":43926411,"strand":-1,"description":"upregulator of cell proliferation [Source:HGNC Symbol;Acc:HGNC:30890]"}, {"versioned_ensembl_gene_id":"ENSG00000243894.1","gene_symbol":"AC116562.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4076711,"end":4077491,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145029.13","gene_symbol":"NICN1","gene_name":"nicolin 1 [Source:HGNC Symbol;Acc:HGNC:18317]","synonyms":"MGC12936","biotype":"protein_coding","ncbi_id":"84276","summary":"This protein encoded by this gene localizes to the nucleus and is expressed in numerous tissues including brain, testis, liver, and kidney. This refseq contains genomic sequence in its 3' UTR which is not supported by experimental evidence. Computer predictions indicate that this region of the 3' UTR contains hairpin-forming self-complementary sequence which is possibly excised after transcription. This gene has a pseudogene on chromosome X. [provided by RefSeq, Jul 2008]","start":49422946,"end":49429326,"strand":-1,"description":"nicolin 1 [Source:HGNC Symbol;Acc:HGNC:18317]"}, {"versioned_ensembl_gene_id":"ENSG00000250940.1","gene_symbol":"AC116562.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4086638,"end":4086814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250476.1","gene_symbol":"ENPP7P9","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48692]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421803","summary":null,"start":3967034,"end":3967660,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48692]"}, {"versioned_ensembl_gene_id":"ENSG00000235794.1","gene_symbol":"MTND3P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52167]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075198","summary":null,"start":93924386,"end":93924716,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:52167]"}, {"versioned_ensembl_gene_id":"ENSG00000100242.15","gene_symbol":"SUN2","gene_name":"Sad1 and UNC84 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:14210]","synonyms":"UNC84B","biotype":"protein_coding","ncbi_id":"25777","summary":"SUN1 (MIM 607723) and SUN2 are inner nuclear membrane (INM) proteins that play a major role in nuclear-cytoplasmic connection by formation of a 'bridge' across the nuclear envelope, known as the LINC complex, via interaction with the conserved luminal KASH domain of nesprins (e.g., SYNE1; MIM 608441) located in the outer nuclear membrane (ONM). The LINC complex provides a direct connection between the nuclear lamina and the cytoskeleton, which contributes to nuclear positioning and cellular rigidity (summary by Haque et al., 2010 [PubMed 19933576]).[supplied by OMIM, Nov 2010]","start":38734725,"end":38794143,"strand":-1,"description":"Sad1 and UNC84 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:14210]"}, {"versioned_ensembl_gene_id":"ENSG00000237984.3","gene_symbol":"PTENP1","gene_name":"phosphatase and tensin homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9589]","synonyms":"PTEN-rs,psiPTEN,PTH2,PTENpg1,PTEN2","biotype":"transcribed_processed_pseudogene","ncbi_id":"11191","summary":"PTENP1 represents a highly homologous processed pseudogene of PTEN (phosphatase and tensin homolog), a protein that encodes a tumor suppressor that functions by negatively regulating the AKT/PKB signaling pathway. PTENP1 is found on chromosome 9 and regulates PTEN by both sense and antisense RNAs (Gene ID: 101243555). This long-noncoding RNA (lncRNA) acts as a decoy for PTEN targeting microRNAs and also exerts a tumor suppressive activity. [provided by RefSeq, Jun 2020]","start":33673504,"end":33677499,"strand":-1,"description":"phosphatase and tensin homolog pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9589]"}, {"versioned_ensembl_gene_id":"ENSG00000276340.4","gene_symbol":"ZNF623","gene_name":"zinc finger protein 623 [Source:HGNC Symbol;Acc:HGNC:29084]","synonyms":"KIAA0628","biotype":"protein_coding","ncbi_id":"9831","summary":null,"start":143621803,"end":143641845,"strand":1,"description":"zinc finger protein 623 [Source:HGNC Symbol;Acc:HGNC:29084]"}, {"versioned_ensembl_gene_id":"ENSG00000205890.3","gene_symbol":"AC108134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3032481,"end":3039133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269153.1","gene_symbol":"LYPLA2P2","gene_name":"lysophospholipase II pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50445]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388499","summary":null,"start":7879445,"end":7880120,"strand":-1,"description":"lysophospholipase II pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50445]"}, {"versioned_ensembl_gene_id":"ENSG00000283401.1","gene_symbol":"AC135068.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21614118,"end":21615038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230149.2","gene_symbol":"AL021707.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38734730,"end":38738990,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280724.1","gene_symbol":"AC183088.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21514144,"end":21567053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163221.8","gene_symbol":"S100A12","gene_name":"S100 calcium binding protein A12 [Source:HGNC Symbol;Acc:HGNC:10489]","synonyms":"MRP6,ENRAGE,CGRP,CAGC,CAAF1,p6","biotype":"protein_coding","ncbi_id":"6283","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein is proposed to be involved in specific calcium-dependent signal transduction pathways and its regulatory effect on cytoskeletal components may modulate various neutrophil activities. The protein includes an antimicrobial peptide which has antibacterial activity. [provided by RefSeq, Nov 2014]","start":153373706,"end":153375649,"strand":-1,"description":"S100 calcium binding protein A12 [Source:HGNC Symbol;Acc:HGNC:10489]"}, {"versioned_ensembl_gene_id":"ENSG00000280709.2","gene_symbol":"LINC02203","gene_name":"long intergenic non-protein coding RNA 2203 [Source:HGNC Symbol;Acc:HGNC:53069]","synonyms":null,"biotype":"lincRNA","ncbi_id":"727924","summary":null,"start":21552795,"end":21653276,"strand":1,"description":"long intergenic non-protein coding RNA 2203 [Source:HGNC Symbol;Acc:HGNC:53069]"}, {"versioned_ensembl_gene_id":"ENSG00000233069.1","gene_symbol":"AL663074.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20732880,"end":20733952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187954.12","gene_symbol":"CYHR1","gene_name":"cysteine and histidine rich 1 [Source:HGNC Symbol;Acc:HGNC:17806]","synonyms":"MGC13010,KIAA0496,CHRP","biotype":"protein_coding","ncbi_id":"50626","summary":null,"start":144449582,"end":144465677,"strand":-1,"description":"cysteine and histidine rich 1 [Source:HGNC Symbol;Acc:HGNC:17806]"}, {"versioned_ensembl_gene_id":"ENSG00000278944.1","gene_symbol":"AC027045.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9791227,"end":9808855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184544.11","gene_symbol":"DHRS7C","gene_name":"dehydrogenase/reductase 7C [Source:HGNC Symbol;Acc:HGNC:32423]","synonyms":"SDR32C2","biotype":"protein_coding","ncbi_id":"201140","summary":null,"start":9771434,"end":9791297,"strand":-1,"description":"dehydrogenase/reductase 7C [Source:HGNC Symbol;Acc:HGNC:32423]"}, {"versioned_ensembl_gene_id":"ENSG00000282882.1","gene_symbol":"AC027045.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9764188,"end":9805073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150628.6","gene_symbol":"SPATA4","gene_name":"spermatogenesis associated 4 [Source:HGNC Symbol;Acc:HGNC:17333]","synonyms":"TSARG2,SPEF1B","biotype":"protein_coding","ncbi_id":"132851","summary":null,"start":176184638,"end":176195671,"strand":-1,"description":"spermatogenesis associated 4 [Source:HGNC Symbol;Acc:HGNC:17333]"}, {"versioned_ensembl_gene_id":"ENSG00000134046.11","gene_symbol":"MBD2","gene_name":"methyl-CpG binding domain protein 2 [Source:HGNC Symbol;Acc:HGNC:6917]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8932","summary":"DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. The protein encoded by this gene may function as a mediator of the biological consequences of the methylation signal. It is also reported that the this protein functions as a demethylase to activate transcription, as DNA methylation causes gene silencing. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]","start":54151601,"end":54224788,"strand":-1,"description":"methyl-CpG binding domain protein 2 [Source:HGNC Symbol;Acc:HGNC:6917]"}, {"versioned_ensembl_gene_id":"ENSG00000169548.3","gene_symbol":"ZNF280A","gene_name":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]","synonyms":"ZNF636,ZNF280,SUHW1,3'OY11.1","biotype":"protein_coding","ncbi_id":"129025","summary":"This gene encodes a zinc finger protein. The encoded protein contains 4 C2H2-type zinc fingers, which are commonly found in transcription factors. A variety of functions may be performed by this type of zinc finger protein, including the binding of DNA or RNA. [provided by RefSeq, Apr 2014]","start":22513736,"end":22520270,"strand":-1,"description":"zinc finger protein 280A [Source:HGNC Symbol;Acc:HGNC:18597]"}, {"versioned_ensembl_gene_id":"ENSG00000099954.18","gene_symbol":"CECR2","gene_name":"CECR2, histone acetyl-lysine reader [Source:HGNC Symbol;Acc:HGNC:1840]","synonyms":"KIAA1740","biotype":"protein_coding","ncbi_id":"27443","summary":"This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":17359949,"end":17558149,"strand":1,"description":"CECR2, histone acetyl-lysine reader [Source:HGNC Symbol;Acc:HGNC:1840]"}, {"versioned_ensembl_gene_id":"ENSG00000189409.13","gene_symbol":"MMP23B","gene_name":"matrix metallopeptidase 23B [Source:HGNC Symbol;Acc:HGNC:7171]","synonyms":"MMP22,MIFR-1,MIFR","biotype":"protein_coding","ncbi_id":"8510","summary":"This gene (MMP23B) encodes a member of the matrix metalloproteinase (MMP) family, and it is part of a duplicated region of chromosome 1p36.3. Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. This gene belongs to the more telomeric copy of the duplicated region. [provided by RefSeq, Jul 2008]","start":1632095,"end":1635263,"strand":1,"description":"matrix metallopeptidase 23B [Source:HGNC Symbol;Acc:HGNC:7171]"}, {"versioned_ensembl_gene_id":"ENSG00000213559.4","gene_symbol":"HNRNPA1P64","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:48794]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129325","summary":null,"start":80451083,"end":80452004,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:48794]"}, {"versioned_ensembl_gene_id":"ENSG00000145103.12","gene_symbol":"ILDR1","gene_name":"immunoglobulin like domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:28741]","synonyms":"MGC50831,DFNB42","biotype":"protein_coding","ncbi_id":"286676","summary":"This gene encodes a protein that contains an immunoglobulin-like domain. The encoded protein may function as a multimeric receptor at the cell surface. The expression of this gene may be a diagnostic marker for cancer progression. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":121987323,"end":122022204,"strand":-1,"description":"immunoglobulin like domain containing receptor 1 [Source:HGNC Symbol;Acc:HGNC:28741]"}, {"versioned_ensembl_gene_id":"ENSG00000159527.3","gene_symbol":"PGLYRP3","gene_name":"peptidoglycan recognition protein 3 [Source:HGNC Symbol;Acc:HGNC:30014]","synonyms":"PGRPIA,PGRP-Ialpha,PGLYRPIalpha","biotype":"protein_coding","ncbi_id":"114771","summary":"This gene encodes a peptidoglycan recognition protein, which belongs to the N-acetylmuramoyl-L-alanine amidase 2 family. These proteins are part of the innate immune system and recognize peptidoglycan, a ubiquitous component of bacterial cell walls. This antimicrobial protein binds to murein peptidoglycans of Gram-positive bacteria. [provided by RefSeq, Oct 2014]","start":153297862,"end":153310718,"strand":-1,"description":"peptidoglycan recognition protein 3 [Source:HGNC Symbol;Acc:HGNC:30014]"}, {"versioned_ensembl_gene_id":"ENSG00000276298.1","gene_symbol":"AC234782.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":103909126,"end":103909449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100055.20","gene_symbol":"CYTH4","gene_name":"cytohesin 4 [Source:HGNC Symbol;Acc:HGNC:9505]","synonyms":"PSCD4,cytohesin-4,CYT4","biotype":"protein_coding","ncbi_id":"27128","summary":"This gene encodes a member of the PSCD family of proteins, which have an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family function as GEPs for ADP-ribosylation factors (ARFs), which are guanine nucleotide-binding proteins involved in vesicular trafficking pathways. This protein exhibits GEP activity in vitro with ARF1 and ARF5, but is inactive with ARF6. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":37282027,"end":37315345,"strand":1,"description":"cytohesin 4 [Source:HGNC Symbol;Acc:HGNC:9505]"}, {"versioned_ensembl_gene_id":"ENSG00000164112.12","gene_symbol":"TMEM155","gene_name":"transmembrane protein 155 [Source:HGNC Symbol;Acc:HGNC:26418]","synonyms":"FLJ30834","biotype":"protein_coding","ncbi_id":"132332","summary":null,"start":121758933,"end":121765427,"strand":-1,"description":"transmembrane protein 155 [Source:HGNC Symbol;Acc:HGNC:26418]"}, {"versioned_ensembl_gene_id":"ENSG00000053702.14","gene_symbol":"NRIP2","gene_name":"nuclear receptor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23078]","synonyms":"DKFZP761G1913","biotype":"protein_coding","ncbi_id":"83714","summary":null,"start":2825348,"end":2835544,"strand":-1,"description":"nuclear receptor interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:23078]"}, {"versioned_ensembl_gene_id":"ENSG00000228739.1","gene_symbol":"AL162384.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6047360,"end":6066714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231334.1","gene_symbol":"AC104781.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54747103,"end":54748404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267156.1","gene_symbol":"TPMTP1","gene_name":"thiopurine S-methyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17490]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400650","summary":null,"start":47630112,"end":47630848,"strand":1,"description":"thiopurine S-methyltransferase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17490]"}, {"versioned_ensembl_gene_id":"ENSG00000160202.7","gene_symbol":"CRYAA","gene_name":"crystallin alpha A [Source:HGNC Symbol;Acc:HGNC:2388]","synonyms":"HSPB4,CRYA1","biotype":"protein_coding","ncbi_id":"1409","summary":"Mammalian lens crystallins are divided into alpha, beta, and gamma families. Alpha crystallins are composed of two gene products: alpha-A and alpha-B, for acidic and basic, respectively. Alpha crystallins can be induced by heat shock and are members of the small heat shock protein (HSP20) family. They act as molecular chaperones although they do not renature proteins and release them in the fashion of a true chaperone; instead they hold them in large soluble aggregates. Post-translational modifications decrease the ability to chaperone. These heterogeneous aggregates consist of 30-40 subunits; the alpha-A and alpha-B subunits have a 3:1 ratio, respectively. Two additional functions of alpha crystallins are an autokinase activity and participation in the intracellular architecture. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alpha-A and alpha-B gene products are differentially expressed; alpha-A is preferentially restricted to the lens and alpha-B is expressed widely in many tissues and organs. Defects in this gene cause autosomal dominant congenital cataract (ADCC). [provided by RefSeq, Jan 2014]","start":43169008,"end":43172805,"strand":1,"description":"crystallin alpha A [Source:HGNC Symbol;Acc:HGNC:2388]"}, {"versioned_ensembl_gene_id":"ENSG00000128191.15","gene_symbol":"DGCR8","gene_name":"DGCR8, microprocessor complex subunit [Source:HGNC Symbol;Acc:HGNC:2847]","synonyms":"pasha,Gy1,DGCRK6,C22orf12","biotype":"protein_coding","ncbi_id":"54487","summary":"This gene encodes a subunit of the microprocessor complex which mediates the biogenesis of microRNAs from the primary microRNA transcript. The encoded protein is a double-stranded RNA binding protein that functions as the non-catalytic subunit of the microprocessor complex. This protein is required for binding the double-stranded RNA substrate and facilitates cleavage of the RNA by the ribonuclease III protein, Drosha. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":20080232,"end":20111877,"strand":1,"description":"DGCR8, microprocessor complex subunit [Source:HGNC Symbol;Acc:HGNC:2847]"}, {"versioned_ensembl_gene_id":"ENSG00000240654.6","gene_symbol":"C1QTNF9","gene_name":"C1q and TNF related 9 [Source:HGNC Symbol;Acc:HGNC:28732]","synonyms":"MGC48915,CTRP9,C1QTNF9A,AQL1","biotype":"protein_coding","ncbi_id":"338872","summary":null,"start":24307166,"end":24322535,"strand":1,"description":"C1q and TNF related 9 [Source:HGNC Symbol;Acc:HGNC:28732]"}, {"versioned_ensembl_gene_id":"ENSG00000228741.2","gene_symbol":"SPATA13","gene_name":"spermatogenesis associated 13 [Source:NCBI gene;Acc:221178]","synonyms":"ASEF2,FLJ31208,ARHGEF29,ARHGEF29","biotype":"lincRNA","ncbi_id":"221178","summary":null,"start":23979810,"end":24035027,"strand":1,"description":"spermatogenesis associated 13 [Source:NCBI gene;Acc:221178]"}, {"versioned_ensembl_gene_id":"ENSG00000224145.8","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"RNF93,ZNFB7,ZNF178","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30153602,"end":30163092,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000270773.1","gene_symbol":"AC137695.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129345411,"end":129346164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231116.9","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31844536,"end":31862971,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000261063.1","gene_symbol":"AC009139.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77201474,"end":77249957,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099901.16","gene_symbol":"RANBP1","gene_name":"RAN binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9847]","synonyms":"HTF9A","biotype":"protein_coding","ncbi_id":"5902","summary":"This gene encodes a protein that forms a complex with Ras-related nuclear protein (Ran) and metabolizes guanoside triphosphate (GTP). This complex participates in the regulation of the cell cycle by controlling transport of proteins and nucleic acids into the nucleus. There are multiple pseudogenes for this gene on chromosomes 9, 12, 17, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":20115938,"end":20127357,"strand":1,"description":"RAN binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9847]"}, {"versioned_ensembl_gene_id":"ENSG00000205274.3","gene_symbol":"TRBV20OR9-2","gene_name":"T-cell receptor beta variable 20/OR9-2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12197]","synonyms":"TRBV20/OR9-2,TCRBV2S2O,TCRBV2O,TCRBV20S2","biotype":"TR_V_gene","ncbi_id":"6962","summary":null,"start":33617762,"end":33618506,"strand":1,"description":"T-cell receptor beta variable 20/OR9-2 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12197]"}, {"versioned_ensembl_gene_id":"ENSG00000281775.2","gene_symbol":"FTCD","gene_name":"formimidoyltransferase cyclodeaminase [Source:HGNC Symbol;Acc:HGNC:3974]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10841","summary":"The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]","start":46142109,"end":46155567,"strand":-1,"description":"formimidoyltransferase cyclodeaminase [Source:HGNC Symbol;Acc:HGNC:3974]"}, {"versioned_ensembl_gene_id":"ENSG00000117245.12","gene_symbol":"KIF17","gene_name":"kinesin family member 17 [Source:HGNC Symbol;Acc:HGNC:19167]","synonyms":"OSM-3,KLP-2,KIF3X,KIF17B,KIAA1405","biotype":"protein_coding","ncbi_id":"57576","summary":null,"start":20664014,"end":20718017,"strand":-1,"description":"kinesin family member 17 [Source:HGNC Symbol;Acc:HGNC:19167]"}, {"versioned_ensembl_gene_id":"ENSG00000226562.3","gene_symbol":"CYP4F26P","gene_name":"cytochrome P450 family 4 subfamily F member 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:39948]","synonyms":"CYP4F-se2[6]","biotype":"lincRNA","ncbi_id":"106478958","summary":null,"start":33580695,"end":33605293,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:39948]"}, {"versioned_ensembl_gene_id":"ENSG00000234373.1","gene_symbol":"SNX18P7","gene_name":"sorting nexin 18 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418980","summary":null,"start":33576380,"end":33577014,"strand":1,"description":"sorting nexin 18 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39615]"}, {"versioned_ensembl_gene_id":"ENSG00000225123.2","gene_symbol":"AL139008.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33574361,"end":33574588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242516.1","gene_symbol":"LINC00960","gene_name":"long intergenic non-protein coding RNA 960 [Source:HGNC Symbol;Acc:HGNC:48710]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401074","summary":null,"start":75672391,"end":75679303,"strand":1,"description":"long intergenic non-protein coding RNA 960 [Source:HGNC Symbol;Acc:HGNC:48710]"}, {"versioned_ensembl_gene_id":"ENSG00000253764.1","gene_symbol":"AC019257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1972570,"end":1974637,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248333.8","gene_symbol":"CDK11B","gene_name":"cyclin dependent kinase 11B [Source:HGNC Symbol;Acc:HGNC:1729]","synonyms":"CDK11-p46,CDK11-p110,CDC2L1,CDK11-p58","biotype":"protein_coding","ncbi_id":"984","summary":"This gene encodes a member of the serine/threonine protein kinase family. Members of this kinase family are known to be essential for eukaryotic cell cycle control. Due to a segmental duplication, this gene shares very high sequence identity with a neighboring gene. These two genes are frequently deleted or altered in neuroblastoma. The protein kinase encoded by this gene can be cleaved by caspases and may play a role in cell apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":1635227,"end":1659012,"strand":-1,"description":"cyclin dependent kinase 11B [Source:HGNC Symbol;Acc:HGNC:1729]"}, {"versioned_ensembl_gene_id":"ENSG00000185078.3","gene_symbol":"AC093698.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":208031383,"end":208031953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280384.1","gene_symbol":"FP325332.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":46163303,"end":46165347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279321.1","gene_symbol":"AC018692.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9913117,"end":9914846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229552.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29887829,"end":29888960,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000231207.1","gene_symbol":"FO393419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27389468,"end":27390145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236041.1","gene_symbol":"COX6CP18","gene_name":"cytochrome c oxidase subunit 6C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481684","summary":null,"start":2771356,"end":2771577,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49370]"}, {"versioned_ensembl_gene_id":"ENSG00000048342.15","gene_symbol":"CC2D2A","gene_name":"coiled-coil and C2 domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29253]","synonyms":"MKS6,KIAA1345,JBTS9","biotype":"protein_coding","ncbi_id":"57545","summary":"This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":15469865,"end":15601557,"strand":1,"description":"coiled-coil and C2 domain containing 2A [Source:HGNC Symbol;Acc:HGNC:29253]"}, {"versioned_ensembl_gene_id":"ENSG00000261762.1","gene_symbol":"AC027228.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78589123,"end":78591276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269821.1","gene_symbol":"KCNQ1OT1","gene_name":"KCNQ1 opposite strand/antisense transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6295]","synonyms":"LIT1,KvLQT1-AS,KvDMR1,KCNQ1-AS2,NCRNA00012","biotype":"antisense_RNA","ncbi_id":"10984","summary":"Human chromosomal region 11p15.5 contains two clusters of epigenetically-regulated genes that are expressed from only one chromosome in a parent-of-origin manner. Each cluster, or imprinted domain, is regulated by a functionally independent imprinting control region (ICR). The human CDKN1C/KCNQ1OT1 domain is regulated by an ICR located in an intron of KCNQ1, and contains at least eight genes that are expressed exclusively or preferentially from the maternally-inherited allele. The DNA of the ICR is specifically methylated on the maternally-inherited chromosome, and unmethylated on the paternally-inherited chromosome. The ICR contains the promoter of the KCNQ1OT1 gene that is exclusively expressed from the paternal allele. The KCNQ1OT1 transcript is the antisense to the KCNQ1 gene and is a unspliced long non-coding RNA. It interacts with chromatin and regulates transcription of multiple target genes through epigenetic modifications. The transcript is abnormally expressed from both chromosomes in most patients with Beckwith-Wiedemann syndrome, and the transcript also plays an important role in colorectal carcinogenesis. [provided by RefSeq, Apr 2012]","start":2608328,"end":2699994,"strand":-1,"description":"KCNQ1 opposite strand/antisense transcript 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:6295]"}, {"versioned_ensembl_gene_id":"ENSG00000101470.9","gene_symbol":"TNNC2","gene_name":"troponin C2, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11944]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7125","summary":"Troponin (Tn), a key protein complex in the regulation of striated muscle contraction, is composed of 3 subunits. The Tn-I subunit inhibits actomyosin ATPase, the Tn-T subunit binds tropomyosin and Tn-C, while the Tn-C subunit binds calcium and overcomes the inhibitory action of the troponin complex on actin filaments. The protein encoded by this gene is the Tn-C subunit. [provided by RefSeq, Jul 2008]","start":45823214,"end":45833745,"strand":-1,"description":"troponin C2, fast skeletal type [Source:HGNC Symbol;Acc:HGNC:11944]"}, {"versioned_ensembl_gene_id":"ENSG00000248370.1","gene_symbol":"LINC02434","gene_name":"long intergenic non-protein coding RNA 2434 [Source:HGNC Symbol;Acc:HGNC:53365]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377606","summary":null,"start":188160065,"end":188161139,"strand":1,"description":"long intergenic non-protein coding RNA 2434 [Source:HGNC Symbol;Acc:HGNC:53365]"}, {"versioned_ensembl_gene_id":"ENSG00000261456.5","gene_symbol":"TUBB8","gene_name":"tubulin beta 8 class VIII [Source:HGNC Symbol;Acc:HGNC:20773]","synonyms":"bA631M21.2","biotype":"protein_coding","ncbi_id":"347688","summary":"The protein encoded by this gene represents the primary beta-tubulin subunit of oocytes and the early embryo. Defects in this gene, which is primate-specific, are a cause of oocyte maturation defect 2 and infertility. [provided by RefSeq, Mar 2016]","start":46892,"end":74163,"strand":-1,"description":"tubulin beta 8 class VIII [Source:HGNC Symbol;Acc:HGNC:20773]"}, {"versioned_ensembl_gene_id":"ENSG00000223914.2","gene_symbol":"LINC02471","gene_name":"long intergenic non-protein coding RNA 2471 [Source:HGNC Symbol;Acc:HGNC:53410]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369734","summary":null,"start":40156113,"end":40211419,"strand":1,"description":"long intergenic non-protein coding RNA 2471 [Source:HGNC Symbol;Acc:HGNC:53410]"}, {"versioned_ensembl_gene_id":"ENSG00000235643.1","gene_symbol":"LINC01647","gene_name":"long intergenic non-protein coding RNA 1647 [Source:HGNC Symbol;Acc:HGNC:52434]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929181","summary":null,"start":11609531,"end":11613355,"strand":1,"description":"long intergenic non-protein coding RNA 1647 [Source:HGNC Symbol;Acc:HGNC:52434]"}, {"versioned_ensembl_gene_id":"ENSG00000238069.1","gene_symbol":"RPLP0P7","gene_name":"ribosomal protein lateral stalk subunit P0 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36578]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271047","summary":null,"start":156777706,"end":156778372,"strand":-1,"description":"ribosomal protein lateral stalk subunit P0 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36578]"}, {"versioned_ensembl_gene_id":"ENSG00000256670.1","gene_symbol":"AC078962.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64599078,"end":64609459,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233339.1","gene_symbol":"AC018878.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106179542,"end":106183797,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232253.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29849309,"end":29849437,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000228084.1","gene_symbol":"AC118553.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99968383,"end":99969864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260370.1","gene_symbol":"AC215217.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14061,"end":16544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223791.1","gene_symbol":"UBE2E1-AS1","gene_name":"UBE2E1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40598]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874092","summary":null,"start":23804024,"end":23806905,"strand":-1,"description":"UBE2E1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40598]"}, {"versioned_ensembl_gene_id":"ENSG00000279367.1","gene_symbol":"AC102797.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47501172,"end":47503106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282912.1","gene_symbol":"AC108724.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75624899,"end":75625188,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281603.2","gene_symbol":"LINC00969","gene_name":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]","synonyms":"ENST00000453324","biotype":"lincRNA","ncbi_id":"440993","summary":null,"start":195658062,"end":195776742,"strand":1,"description":"long intergenic non-protein coding RNA 969 [Source:HGNC Symbol;Acc:HGNC:48729]"}, {"versioned_ensembl_gene_id":"ENSG00000243422.2","gene_symbol":"RPL23AP49","gene_name":"ribosomal protein L23a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35689]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"653236","summary":null,"start":75624275,"end":75670156,"strand":-1,"description":"ribosomal protein L23a pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:35689]"}, {"versioned_ensembl_gene_id":"ENSG00000261486.1","gene_symbol":"RARRES2P9","gene_name":"retinoic acid receptor responder 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106660620","summary":null,"start":35344091,"end":35344559,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:48708]"}, {"versioned_ensembl_gene_id":"ENSG00000269763.1","gene_symbol":"EXOSC3P2","gene_name":"exosome component 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33990]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100190954","summary":null,"start":7813615,"end":7814425,"strand":-1,"description":"exosome component 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33990]"}, {"versioned_ensembl_gene_id":"ENSG00000270168.2","gene_symbol":"AC004233.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2988256,"end":3002016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266938.1","gene_symbol":"AC119403.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2896625,"end":2897222,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244222.2","gene_symbol":"OR7E121P","gene_name":"olfactory receptor family 7 subfamily E member 121 pseudogene [Source:HGNC Symbol;Acc:HGNC:15049]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402133","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":75598652,"end":75599673,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 121 pseudogene [Source:HGNC Symbol;Acc:HGNC:15049]"}, {"versioned_ensembl_gene_id":"ENSG00000239383.1","gene_symbol":"AC108724.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75590298,"end":75590649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125888.14","gene_symbol":"BANF2","gene_name":"barrier to autointegration factor 2 [Source:HGNC Symbol;Acc:HGNC:16172]","synonyms":"dJ803K15.1,C20orf179,BAFL,BAF2,BAF-L","biotype":"protein_coding","ncbi_id":"140836","summary":null,"start":17693672,"end":17735871,"strand":1,"description":"barrier to autointegration factor 2 [Source:HGNC Symbol;Acc:HGNC:16172]"}, {"versioned_ensembl_gene_id":"ENSG00000272710.2","gene_symbol":"AC133041.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75540049,"end":75580199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231923.1","gene_symbol":"AC024082.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138046654,"end":138047897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233478.1","gene_symbol":"AL031280.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25644544,"end":25659111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267571.1","gene_symbol":"AC104532.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5911578,"end":5913899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227427.1","gene_symbol":"Z93019.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57766320,"end":57767292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198153.8","gene_symbol":"ZNF849P","gene_name":"zinc finger protein 849, pseudogene [Source:HGNC Symbol;Acc:HGNC:34389]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130108","summary":null,"start":22685167,"end":22686732,"strand":1,"description":"zinc finger protein 849, pseudogene [Source:HGNC Symbol;Acc:HGNC:34389]"}, {"versioned_ensembl_gene_id":"ENSG00000088247.17","gene_symbol":"KHSRP","gene_name":"KH-type splicing regulatory protein [Source:HGNC Symbol;Acc:HGNC:6316]","synonyms":"KSRP,FUBP2,FBP2","biotype":"protein_coding","ncbi_id":"8570","summary":"The KHSRP gene encodes a multifunctional RNA-binding protein implicated in a variety of cellular processes, including transcription, alternative pre-mRNA splicing, and mRNA localization (Min et al., 1997 [PubMed 9136930]; Gherzi et al., 2004 [PubMed 15175153]).[supplied by OMIM, Apr 2010]","start":6413348,"end":6424794,"strand":-1,"description":"KH-type splicing regulatory protein [Source:HGNC Symbol;Acc:HGNC:6316]"}, {"versioned_ensembl_gene_id":"ENSG00000231397.1","gene_symbol":"AC004941.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149321865,"end":149322092,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248476.1","gene_symbol":"BACH1-IT1","gene_name":"BACH1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:40006]","synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29351634,"end":29361894,"strand":1,"description":"BACH1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:40006]"}, {"versioned_ensembl_gene_id":"ENSG00000273017.1","gene_symbol":"AP000240.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29359002,"end":29359453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101000.5","gene_symbol":"PROCR","gene_name":"protein C receptor [Source:HGNC Symbol;Acc:HGNC:9452]","synonyms":"EPCR,CD201,CCD41","biotype":"protein_coding","ncbi_id":"10544","summary":"The protein encoded by this gene is a receptor for activated protein C, a serine protease activated by and involved in the blood coagulation pathway. The encoded protein is an N-glycosylated type I membrane protein that enhances the activation of protein C. Mutations in this gene have been associated with venous thromboembolism and myocardial infarction, as well as with late fetal loss during pregnancy. The encoded protein may also play a role in malarial infection and has been associated with cancer. [provided by RefSeq, Jul 2013]","start":35172073,"end":35216240,"strand":1,"description":"protein C receptor [Source:HGNC Symbol;Acc:HGNC:9452]"}, {"versioned_ensembl_gene_id":"ENSG00000225731.1","gene_symbol":"AP001627.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42733594,"end":42741758,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278367.1","gene_symbol":"AL356652.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35174355,"end":35174919,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213462.4","gene_symbol":"ERV3-1","gene_name":"endogenous retrovirus group 3 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:3454]","synonyms":"HERV-R,H-PLK,ERV3,ERV-R,envR","biotype":"protein_coding","ncbi_id":"2086","summary":"This gene contains sequence derived from endogenous retrovirus, and is therefore similar to multiple other loci in the genome. Transcripts at this locus encode a conserved protein with a predicted signal peptide and similarity to the Env polyprotein. This protein is overexpressed in colorectal and other cancers. [provided by RefSeq, Jan 2017]","start":64990809,"end":65006743,"strand":-1,"description":"endogenous retrovirus group 3 member 1, envelope [Source:HGNC Symbol;Acc:HGNC:3454]"}, {"versioned_ensembl_gene_id":"ENSG00000262282.2","gene_symbol":"AC003958.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41334632,"end":41335733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146592.16","gene_symbol":"CREB5","gene_name":"cAMP responsive element binding protein 5 [Source:HGNC Symbol;Acc:HGNC:16844]","synonyms":"H_GS165L15.1,CRE-BPA","biotype":"protein_coding","ncbi_id":"9586","summary":"The product of this gene belongs to the CRE (cAMP response element)-binding protein family. Members of this family contain zinc-finger and bZIP DNA-binding domains. The encoded protein specifically binds to CRE as a homodimer or a heterodimer with c-Jun or CRE-BP1, and functions as a CRE-dependent trans-activator. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":28299321,"end":28825894,"strand":1,"description":"cAMP responsive element binding protein 5 [Source:HGNC Symbol;Acc:HGNC:16844]"}, {"versioned_ensembl_gene_id":"ENSG00000236686.1","gene_symbol":"BZW1P1","gene_name":"basic leucine zipper and W2 domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31378]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391592","summary":null,"start":172425850,"end":172427089,"strand":-1,"description":"basic leucine zipper and W2 domains 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31378]"}, {"versioned_ensembl_gene_id":"ENSG00000270762.1","gene_symbol":"FXYD6P1","gene_name":"FXYD domain containing ion transport regulator 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4031]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128934","summary":null,"start":42555440,"end":42555724,"strand":1,"description":"FXYD domain containing ion transport regulator 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4031]"}, {"versioned_ensembl_gene_id":"ENSG00000163209.14","gene_symbol":"SPRR3","gene_name":"small proline rich protein 3 [Source:HGNC Symbol;Acc:HGNC:11268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6707","summary":null,"start":153001747,"end":153003856,"strand":1,"description":"small proline rich protein 3 [Source:HGNC Symbol;Acc:HGNC:11268]"}, {"versioned_ensembl_gene_id":"ENSG00000205936.3","gene_symbol":"PPP1R12BP2","gene_name":"protein phosphatase 1 regulatory subunit 12B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23970]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"360020","summary":null,"start":23379484,"end":23392697,"strand":1,"description":"protein phosphatase 1 regulatory subunit 12B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23970]"}, {"versioned_ensembl_gene_id":"ENSG00000220205.8","gene_symbol":"VAMP2","gene_name":"vesicle associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:12643]","synonyms":"VAMP-2,SYB2","biotype":"protein_coding","ncbi_id":"6844","summary":"The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. This gene is thought to participate in neurotransmitter release at a step between docking and fusion. The protein forms a stable complex with syntaxin, synaptosomal-associated protein, 25 kD, and synaptotagmin. It also forms a distinct complex with synaptophysin. It is a likely candidate gene for familial infantile myasthenia (FIMG) because of its map location and because it encodes a synaptic vesicle protein of the type that has been implicated in the pathogenesis of FIMG. [provided by RefSeq, Jul 2008]","start":8159149,"end":8163546,"strand":-1,"description":"vesicle associated membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:12643]"}, {"versioned_ensembl_gene_id":"ENSG00000260268.5","gene_symbol":"LINC00919","gene_name":"long intergenic non-protein coding RNA 919 [Source:HGNC Symbol;Acc:HGNC:48610]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505619","summary":null,"start":52083065,"end":52085109,"strand":-1,"description":"long intergenic non-protein coding RNA 919 [Source:HGNC Symbol;Acc:HGNC:48610]"}, {"versioned_ensembl_gene_id":"ENSG00000188706.12","gene_symbol":"ZDHHC9","gene_name":"zinc finger DHHC-type containing 9 [Source:HGNC Symbol;Acc:HGNC:18475]","synonyms":"ZNF380,ZNF379,ZDHHC10,CXorf11,CGI-89","biotype":"protein_coding","ncbi_id":"51114","summary":"This gene encodes an integral membrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein forms a complex with golgin subfamily A member 7 and functions as a palmitoyltransferase. This protein specifically palmitoylates HRAS and NRAS. Mutations in this gene are associated with X-linked cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, May 2010]","start":129803288,"end":129843909,"strand":-1,"description":"zinc finger DHHC-type containing 9 [Source:HGNC Symbol;Acc:HGNC:18475]"}, {"versioned_ensembl_gene_id":"ENSG00000152382.5","gene_symbol":"TADA1","gene_name":"transcriptional adaptor 1 [Source:HGNC Symbol;Acc:HGNC:30631]","synonyms":"hADA1,ADA1,TADA1L,STAF42,HFI1","biotype":"protein_coding","ncbi_id":"117143","summary":"TADA1L is a protein subunit of the human STAGA complex (SPT3; (MIM 602947)/TAF9 (MIM 600822)/GCN5 (MIM 602301) acetyltransferase complex), which is a chromatin-modifying multiprotein complex (Martinez et al., 2001 [PubMed 11564863]).[supplied by OMIM, Apr 2009]","start":166856510,"end":166876327,"strand":-1,"description":"transcriptional adaptor 1 [Source:HGNC Symbol;Acc:HGNC:30631]"}, {"versioned_ensembl_gene_id":"ENSG00000188051.6","gene_symbol":"TMEM221","gene_name":"transmembrane protein 221 [Source:HGNC Symbol;Acc:HGNC:21943]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130519","summary":null,"start":17435509,"end":17448567,"strand":-1,"description":"transmembrane protein 221 [Source:HGNC Symbol;Acc:HGNC:21943]"}, {"versioned_ensembl_gene_id":"ENSG00000135537.16","gene_symbol":"AFG1L","gene_name":"AFG1 like ATPase [Source:HGNC Symbol;Acc:HGNC:16411]","synonyms":"LACE1,AFG1","biotype":"protein_coding","ncbi_id":"246269","summary":"This gene encodes a mitochondrial integral membrane protein that plays a role in mitochondrial protein homeostasis. The protein contains a P-loop motif and a five-domain structure that is conserved in fly, yeast, and bacteria. It functions to mediate the degradation of nuclear-encoded complex IV subunits. Two conserved estrogen receptor binding sites are located within 2.5 kb of this gene. Polymorphisms in this gene have been associated with bipolar disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":108294894,"end":108526796,"strand":1,"description":"AFG1 like ATPase [Source:HGNC Symbol;Acc:HGNC:16411]"}, {"versioned_ensembl_gene_id":"ENSG00000227222.7","gene_symbol":"DHX16","gene_name":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]","synonyms":"DBP2,Prp2,DDX16,PRPF2","biotype":"protein_coding","ncbi_id":"8449","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":30723385,"end":30736950,"strand":-1,"description":"DEAH-box helicase 16 [Source:HGNC Symbol;Acc:HGNC:2739]"}, {"versioned_ensembl_gene_id":"ENSG00000251284.2","gene_symbol":"AC111000.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69125274,"end":69126451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135111.15","gene_symbol":"TBX3","gene_name":"T-box 3 [Source:HGNC Symbol;Acc:HGNC:11602]","synonyms":"XHL,UMS,TBX3-ISO","biotype":"protein_coding","ncbi_id":"6926","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This protein is a transcriptional repressor and is thought to play a role in the anterior/posterior axis of the tetrapod forelimb. Mutations in this gene cause ulnar-mammary syndrome, affecting limb, apocrine gland, tooth, hair, and genital development. Alternative splicing of this gene results in three transcript variants encoding different isoforms; however, the full length nature of one variant has not been determined. [provided by RefSeq, Jul 2008]","start":114670254,"end":114684164,"strand":-1,"description":"T-box 3 [Source:HGNC Symbol;Acc:HGNC:11602]"}, {"versioned_ensembl_gene_id":"ENSG00000230703.1","gene_symbol":"AL591178.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24066774,"end":24083565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261183.5","gene_symbol":"SPINT1-AS1","gene_name":"SPINT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53162]","synonyms":"RP11-532F12.5","biotype":"antisense_RNA","ncbi_id":"102724362","summary":null,"start":40835808,"end":40844387,"strand":-1,"description":"SPINT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53162]"}, {"versioned_ensembl_gene_id":"ENSG00000228172.5","gene_symbol":"AL020996.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25816749,"end":25820797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083635.7","gene_symbol":"NUFIP1","gene_name":"NUFIP1, FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8057]","synonyms":"NUFIP","biotype":"protein_coding","ncbi_id":"26747","summary":"This gene encodes a nuclear RNA binding protein that contains a C2H2 zinc finger motif and a nuclear localization signal. This protein is associated with the nuclear matrix in perichromatin fibrils and, in neurons, localizes to the cytoplasm in association with endoplasmic reticulum ribosomes. This protein interacts with the fragile X mental retardation protein (FMRP), the tumor suppressor protein BRCA1, upregulates RNA polymerase II transcription, and is involved in box C/D snoRNP biogenesis. A pseudogene of this gene resides on chromosome 6q12. [provided by RefSeq, Feb 2012]","start":44939249,"end":44989483,"strand":-1,"description":"NUFIP1, FMR1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8057]"}, {"versioned_ensembl_gene_id":"ENSG00000233691.2","gene_symbol":"AL354714.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160935537,"end":160936126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255284.1","gene_symbol":"AP006621.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":777578,"end":784297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232049.2","gene_symbol":"OR2I1P","gene_name":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]","synonyms":"OR2I2,OR2I4P,OR2I1,OR2I3P,HS6M1-14","biotype":"unprocessed_pseudogene","ncbi_id":"442197","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29553030,"end":29553977,"strand":1,"description":"olfactory receptor family 2 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8258]"}, {"versioned_ensembl_gene_id":"ENSG00000179363.6","gene_symbol":"TMEM31","gene_name":"transmembrane protein 31 [Source:HGNC Symbol;Acc:HGNC:28601]","synonyms":"MGC39655","biotype":"protein_coding","ncbi_id":"203562","summary":null,"start":103710909,"end":103714028,"strand":1,"description":"transmembrane protein 31 [Source:HGNC Symbol;Acc:HGNC:28601]"}, {"versioned_ensembl_gene_id":"ENSG00000244073.1","gene_symbol":"RPS4XP6","gene_name":"ribosomal protein S4X pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36057]","synonyms":"RPS4P6","biotype":"processed_pseudogene","ncbi_id":"391777","summary":null,"start":37085056,"end":37085852,"strand":1,"description":"ribosomal protein S4X pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36057]"}, {"versioned_ensembl_gene_id":"ENSG00000254075.1","gene_symbol":"IGLVV-66","gene_name":"immunoglobulin lambda variable (V)-66 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5946]","synonyms":"IGLV(V)-66","biotype":"IG_V_pseudogene","ncbi_id":"28757","summary":null,"start":22061077,"end":22061538,"strand":1,"description":"immunoglobulin lambda variable (V)-66 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5946]"}, {"versioned_ensembl_gene_id":"ENSG00000249328.2","gene_symbol":"AC036214.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79769372,"end":79871759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227668.1","gene_symbol":"MAS1LP1","gene_name":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]","synonyms":"OTTHUMG00000086553,MAS1LP","biotype":"unprocessed_pseudogene","ncbi_id":"646366","summary":null,"start":29474806,"end":29475852,"strand":-1,"description":"MAS1L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33448]"}, {"versioned_ensembl_gene_id":"ENSG00000106113.18","gene_symbol":"CRHR2","gene_name":"corticotropin releasing hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:2358]","synonyms":"HM-CRF,CRF2,CRF-RB","biotype":"protein_coding","ncbi_id":"1395","summary":"The protein encoded by this gene belongs to the G-protein coupled receptor 2 family, and the subfamily of corticotropin releasing hormone receptor. This receptor shows high affinity for corticotropin releasing hormone (CRH), and also binds CRH-related peptides such as urocortin. CRH is synthesized in the hypothalamus, and plays an important role in coordinating the endocrine, autonomic, and behavioral responses to stress and immune challenge. Studies in mice suggest that this receptor maybe involved in mediating cardiovascular homeostasis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jan 2011]","start":30651943,"end":30700129,"strand":-1,"description":"corticotropin releasing hormone receptor 2 [Source:HGNC Symbol;Acc:HGNC:2358]"}, {"versioned_ensembl_gene_id":"ENSG00000257849.1","gene_symbol":"AC012038.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42966122,"end":42967353,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254355.1","gene_symbol":"IGLVI-68","gene_name":"immunoglobulin lambda variable (I)-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5939]","synonyms":"IGLV(I)-68","biotype":"IG_V_pseudogene","ncbi_id":"28764","summary":null,"start":22032745,"end":22033194,"strand":1,"description":"immunoglobulin lambda variable (I)-68 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5939]"}, {"versioned_ensembl_gene_id":"ENSG00000262106.1","gene_symbol":"AC090282.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":3265611,"end":3266541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253794.1","gene_symbol":"IGLV10-67","gene_name":"immunoglobulin lambda variable 10-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5885]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28771","summary":null,"start":22043618,"end":22043942,"strand":1,"description":"immunoglobulin lambda variable 10-67 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5885]"}, {"versioned_ensembl_gene_id":"ENSG00000234651.10","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31715314,"end":31728984,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000113889.11","gene_symbol":"KNG1","gene_name":"kininogen 1 [Source:HGNC Symbol;Acc:HGNC:6383]","synonyms":"BDK,KNG,BK","biotype":"protein_coding","ncbi_id":"3827","summary":"This gene uses alternative splicing to generate two different proteins- high molecular weight kininogen (HMWK) and low molecular weight kininogen (LMWK). HMWK is essential for blood coagulation and assembly of the kallikrein-kinin system. Also, bradykinin, a peptide causing numerous physiological effects, is released from HMWK. Bradykinin also functions as an antimicrobial peptide with antibacterial and antifungal activity. In contrast to HMWK, LMWK is not involved in blood coagulation. Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) reduces or depletes angiotensin converting enzyme 2 (ACE2), which results in an increase in levels of des-Arg(9)-bradykinin, a bioactive metabolite of bradykinin that is associated with lung injury and inflammation. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2020]","start":186717276,"end":186743954,"strand":1,"description":"kininogen 1 [Source:HGNC Symbol;Acc:HGNC:6383]"}, {"versioned_ensembl_gene_id":"ENSG00000260344.2","gene_symbol":"AC133485.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32213380,"end":32213503,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198205.6","gene_symbol":"ZXDA","gene_name":"zinc finger, X-linked, duplicated A [Source:HGNC Symbol;Acc:HGNC:13198]","synonyms":"ZNF896","biotype":"protein_coding","ncbi_id":"7789","summary":"This gene encodes one of two duplicated zinc finger genes on chromosome Xp11. This gene is the telomeric copy; GeneID 158586 ZXDB is the more centromeric copy. The two genes have 98% nucleotide sequence similarity, and the predicted proteins contain 10 tandem zinc finger motifs. [provided by RefSeq, Nov 2009]","start":57906708,"end":57910820,"strand":-1,"description":"zinc finger, X-linked, duplicated A [Source:HGNC Symbol;Acc:HGNC:13198]"}, {"versioned_ensembl_gene_id":"ENSG00000203942.4","gene_symbol":"C10orf62","gene_name":"chromosome 10 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:23294]","synonyms":"bA548K23.1","biotype":"protein_coding","ncbi_id":"414157","summary":null,"start":97589727,"end":97590934,"strand":1,"description":"chromosome 10 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:23294]"}, {"versioned_ensembl_gene_id":"ENSG00000173511.9","gene_symbol":"VEGFB","gene_name":"vascular endothelial growth factor B [Source:HGNC Symbol;Acc:HGNC:12681]","synonyms":"VRF,VEGFL","biotype":"protein_coding","ncbi_id":"7423","summary":"This gene encodes a member of the PDGF (platelet-derived growth factor)/VEGF (vascular endothelial growth factor) family. The VEGF family members regulate the formation of blood vessels and are involved in endothelial cell physiology. This member is a ligand for VEGFR-1 (vascular endothelial growth factor receptor 1) and NRP-1 (neuropilin-1). Studies in mice showed that this gene was co-expressed with nuclear-encoded mitochondrial genes and the encoded protein specifically controlled endothelial uptake of fatty acids. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Sep 2011]","start":64234538,"end":64238793,"strand":1,"description":"vascular endothelial growth factor B [Source:HGNC Symbol;Acc:HGNC:12681]"}, {"versioned_ensembl_gene_id":"ENSG00000281418.1","gene_symbol":"SDHAP2","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]","synonyms":"SDHAL2,SDHALP2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727956","summary":null,"start":195658096,"end":195685904,"strand":1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:27408]"}, {"versioned_ensembl_gene_id":"ENSG00000249967.1","gene_symbol":"AL355315.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":97584374,"end":97673910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254362.1","gene_symbol":"AC011726.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26440491,"end":26442595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234338.1","gene_symbol":"AC073349.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64835280,"end":64836882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224168.9","gene_symbol":"TRIM31","gene_name":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]","synonyms":"HCG1,RNF,C6orf13,HCGI","biotype":"protein_coding","ncbi_id":"11074","summary":"This gene encodes a protein that functions as an E3 ubiquitin-protein ligase. This gene shows altered expression in certain tumors and may be a negative regulator of cell growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30093294,"end":30103494,"strand":-1,"description":"tripartite motif containing 31 [Source:HGNC Symbol;Acc:HGNC:16289]"}, {"versioned_ensembl_gene_id":"ENSG00000253208.1","gene_symbol":"AC015743.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26547669,"end":26548463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205791.3","gene_symbol":"LOH12CR2","gene_name":"loss of heterozygosity, 12, chromosomal region 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26524]","synonyms":"LOH2CR12","biotype":"lincRNA","ncbi_id":"503693","summary":null,"start":12355406,"end":12357067,"strand":-1,"description":"loss of heterozygosity, 12, chromosomal region 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26524]"}, {"versioned_ensembl_gene_id":"ENSG00000008300.16","gene_symbol":"CELSR3","gene_name":"cadherin EGF LAG seven-pass G-type receptor 3 [Source:HGNC Symbol;Acc:HGNC:3230]","synonyms":"MEGF2,HFMI1,FMI1,EGFL1,CDHF11,ADGRC3","biotype":"protein_coding","ncbi_id":"1951","summary":"This gene belongs to the flamingo subfamily, which is included in the cadherin superfamily. The flamingo cadherins consist of nonclassic-type cadherins that do not interact with catenins. They are plasma membrane proteins containing seven epidermal growth factor-like repeats, nine cadherin domains and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic feature of their subfamily. The encoded protein may be involved in the regulation of contact-dependent neurite growth and may play a role in tumor formation. [provided by RefSeq, Jun 2013]","start":48636469,"end":48662915,"strand":-1,"description":"cadherin EGF LAG seven-pass G-type receptor 3 [Source:HGNC Symbol;Acc:HGNC:3230]"}, {"versioned_ensembl_gene_id":"ENSG00000155252.13","gene_symbol":"PI4K2A","gene_name":"phosphatidylinositol 4-kinase type 2 alpha [Source:HGNC Symbol;Acc:HGNC:30031]","synonyms":"PIK42A,PI4KII,DKFZP761G1923","biotype":"protein_coding","ncbi_id":"55361","summary":"Phosphatidylinositolpolyphosphates (PtdInsPs) are centrally involved in many biologic processes, ranging from cell growth and organization of the actin cytoskeleton to endo- and exocytosis. PI4KII phosphorylates PtdIns at the D-4 position, an essential step in the biosynthesis of PtdInsPs (Barylko et al., 2001 [PubMed 11244087]).[supplied by OMIM, Mar 2008]","start":97640686,"end":97676434,"strand":1,"description":"phosphatidylinositol 4-kinase type 2 alpha [Source:HGNC Symbol;Acc:HGNC:30031]"}, {"versioned_ensembl_gene_id":"ENSG00000119922.9","gene_symbol":"IFIT2","gene_name":"interferon induced protein with tetratricopeptide repeats 2 [Source:HGNC Symbol;Acc:HGNC:5409]","synonyms":"ISG-54K,IFI54,IFI-54,GARG-39,G10P2,cig42","biotype":"protein_coding","ncbi_id":"3433","summary":null,"start":89283694,"end":89309276,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 2 [Source:HGNC Symbol;Acc:HGNC:5409]"}, {"versioned_ensembl_gene_id":"ENSG00000092964.17","gene_symbol":"DPYSL2","gene_name":"dihydropyrimidinase like 2 [Source:HGNC Symbol;Acc:HGNC:3014]","synonyms":"DRP2,DRP-2,DHPRP2,CRMP2","biotype":"protein_coding","ncbi_id":"1808","summary":"This gene encodes a member of the collapsin response mediator protein family. Collapsin response mediator proteins form homo- and hetero-tetramers and facilitate neuron guidance, growth and polarity. The encoded protein promotes microtubule assembly and is required for Sema3A-mediated growth cone collapse, and also plays a role in synaptic signaling through interactions with calcium channels. This gene has been implicated in multiple neurological disorders, and hyperphosphorylation of the encoded protein may play a key role in the development of Alzheimer's disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":26514022,"end":26658178,"strand":1,"description":"dihydropyrimidinase like 2 [Source:HGNC Symbol;Acc:HGNC:3014]"}, {"versioned_ensembl_gene_id":"ENSG00000266521.1","gene_symbol":"AC021549.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31496645,"end":31497195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230507.5","gene_symbol":"RPL7AP8","gene_name":"ribosomal protein L7a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23738]","synonyms":"bA141D8.1","biotype":"processed_pseudogene","ncbi_id":"340749","summary":null,"start":86630825,"end":86631628,"strand":-1,"description":"ribosomal protein L7a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:23738]"}, {"versioned_ensembl_gene_id":"ENSG00000218739.9","gene_symbol":"CEBPZOS","gene_name":"CEBPZ opposite strand [Source:HGNC Symbol;Acc:HGNC:49288]","synonyms":"CEBPZ-AS1","biotype":"protein_coding","ncbi_id":"100505876","summary":null,"start":37196488,"end":37216193,"strand":1,"description":"CEBPZ opposite strand [Source:HGNC Symbol;Acc:HGNC:49288]"}, {"versioned_ensembl_gene_id":"ENSG00000227626.1","gene_symbol":"AL662865.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29023286,"end":29024213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268685.1","gene_symbol":"AC011494.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22362589,"end":22362825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260599.1","gene_symbol":"AC011467.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22520995,"end":22527949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234101.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29040820,"end":29041847,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000232110.7","gene_symbol":"AL353751.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89283765,"end":89292125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225838.1","gene_symbol":"AL662852.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29068429,"end":29069201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203469.2","gene_symbol":"AL354956.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10458555,"end":10459338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226657.1","gene_symbol":"AL662852.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29073178,"end":29073773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224289.1","gene_symbol":"IFIT6P","gene_name":"interferon induced protein with tetratricopeptide repeats 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:38020]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100128465","summary":null,"start":89362294,"end":89363487,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:38020]"}, {"versioned_ensembl_gene_id":"ENSG00000235237.1","gene_symbol":"Z82188.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37166757,"end":37182850,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269035.1","gene_symbol":"AC010319.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17436611,"end":17460804,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160049.11","gene_symbol":"DFFA","gene_name":"DNA fragmentation factor subunit alpha [Source:HGNC Symbol;Acc:HGNC:2772]","synonyms":"ICAD,DFF45,DFF1,DFF-45","biotype":"protein_coding","ncbi_id":"1676","summary":"Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":10456522,"end":10472526,"strand":-1,"description":"DNA fragmentation factor subunit alpha [Source:HGNC Symbol;Acc:HGNC:2772]"}, {"versioned_ensembl_gene_id":"ENSG00000130413.15","gene_symbol":"STK33","gene_name":"serine/threonine kinase 33 [Source:HGNC Symbol;Acc:HGNC:14568]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65975","summary":null,"start":8391868,"end":8594289,"strand":-1,"description":"serine/threonine kinase 33 [Source:HGNC Symbol;Acc:HGNC:14568]"}, {"versioned_ensembl_gene_id":"ENSG00000133466.13","gene_symbol":"C1QTNF6","gene_name":"C1q and TNF related 6 [Source:HGNC Symbol;Acc:HGNC:14343]","synonyms":"ZACRP6,CTRP6","biotype":"protein_coding","ncbi_id":"114904","summary":null,"start":37180167,"end":37199385,"strand":-1,"description":"C1q and TNF related 6 [Source:HGNC Symbol;Acc:HGNC:14343]"}, {"versioned_ensembl_gene_id":"ENSG00000119917.13","gene_symbol":"IFIT3","gene_name":"interferon induced protein with tetratricopeptide repeats 3 [Source:HGNC Symbol;Acc:HGNC:5411]","synonyms":"GARG-49,CIG-49,RIG-G,ISG60,IRG2,IFIT4,IFI60","biotype":"protein_coding","ncbi_id":"3437","summary":null,"start":89327894,"end":89340971,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 3 [Source:HGNC Symbol;Acc:HGNC:5411]"}, {"versioned_ensembl_gene_id":"ENSG00000171773.2","gene_symbol":"NXNL1","gene_name":"nucleoredoxin like 1 [Source:HGNC Symbol;Acc:HGNC:25179]","synonyms":"TXNL6,RDCVF","biotype":"protein_coding","ncbi_id":"115861","summary":"Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015]","start":17455425,"end":17460954,"strand":-1,"description":"nucleoredoxin like 1 [Source:HGNC Symbol;Acc:HGNC:25179]"}, {"versioned_ensembl_gene_id":"ENSG00000171160.17","gene_symbol":"MORN4","gene_name":"MORN repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:24001]","synonyms":"rtp,FLJ25925,C10orf83,bA548K23.4","biotype":"protein_coding","ncbi_id":"118812","summary":null,"start":97614553,"end":97633500,"strand":-1,"description":"MORN repeat containing 4 [Source:HGNC Symbol;Acc:HGNC:24001]"}, {"versioned_ensembl_gene_id":"ENSG00000269736.1","gene_symbol":"AC010319.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17452211,"end":17452969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139155.8","gene_symbol":"SLCO1C1","gene_name":"solute carrier organic anion transporter family member 1C1 [Source:HGNC Symbol;Acc:HGNC:13819]","synonyms":"OATP-F,SLC21A14,OATP1C1,OATP1","biotype":"protein_coding","ncbi_id":"53919","summary":"This gene encodes a member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of thyroid hormones in brain tissues. This protein has particularly high affinity for the thyroid hormones thyroxine, tri-iodothyronine and reverse tri-iodothyronine. Polymorphisms in the gene encoding this protein may be associated with fatigue and depression in patients suffering from hyperthyroidism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":20695355,"end":20753386,"strand":1,"description":"solute carrier organic anion transporter family member 1C1 [Source:HGNC Symbol;Acc:HGNC:13819]"}, {"versioned_ensembl_gene_id":"ENSG00000132603.13","gene_symbol":"NIP7","gene_name":"NIP7, nucleolar pre-rRNA processing protein [Source:HGNC Symbol;Acc:HGNC:24328]","synonyms":"FLJ10296,CGI-37,KD93,HSPC031","biotype":"protein_coding","ncbi_id":"51388","summary":null,"start":69339430,"end":69343111,"strand":1,"description":"NIP7, nucleolar pre-rRNA processing protein [Source:HGNC Symbol;Acc:HGNC:24328]"}, {"versioned_ensembl_gene_id":"ENSG00000171453.17","gene_symbol":"POLR1C","gene_name":"RNA polymerase I subunit C [Source:HGNC Symbol;Acc:HGNC:20194]","synonyms":"RPAC1,RPA5,RPA40,RPA39","biotype":"protein_coding","ncbi_id":"9533","summary":"The protein encoded by this gene is a subunit of both RNA polymerase I and RNA polymerase III complexes. The encoded protein is part of the Pol core element. Mutations in this gene have been associated with Treacher Collins syndrome (TCS) and hypomyelinating leukodystrophy 11. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":43509702,"end":43529585,"strand":1,"description":"RNA polymerase I subunit C [Source:HGNC Symbol;Acc:HGNC:20194]"}, {"versioned_ensembl_gene_id":"ENSG00000257181.1","gene_symbol":"AC025423.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68841288,"end":68843237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225732.1","gene_symbol":"TRIM31-AS1","gene_name":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"104533120","summary":null,"start":30095634,"end":30105111,"strand":1,"description":"TRIM31 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39761]"}, {"versioned_ensembl_gene_id":"ENSG00000138068.10","gene_symbol":"SULT6B1","gene_name":"sulfotransferase family 6B member 1 [Source:HGNC Symbol;Acc:HGNC:33433]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391365","summary":null,"start":37167820,"end":37196598,"strand":-1,"description":"sulfotransferase family 6B member 1 [Source:HGNC Symbol;Acc:HGNC:33433]"}, {"versioned_ensembl_gene_id":"ENSG00000227072.1","gene_symbol":"AL353706.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108387512,"end":108388080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238079.1","gene_symbol":"AL356121.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108372772,"end":108372927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277281.3","gene_symbol":"MUC6","gene_name":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"4588","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. [provided by RefSeq, Dec 2016]","start":1019669,"end":1048356,"strand":-1,"description":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]"}, {"versioned_ensembl_gene_id":"ENSG00000238055.1","gene_symbol":"Z98742.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108318079,"end":108318404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237418.1","gene_symbol":"AC069257.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":196298061,"end":196298215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271803.1","gene_symbol":"AL121906.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33674517,"end":33675380,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241935.8","gene_symbol":"HOGA1","gene_name":"4-hydroxy-2-oxoglutarate aldolase 1 [Source:HGNC Symbol;Acc:HGNC:25155]","synonyms":"NPL2,FLJ37472,DHDPSL,DHDPS2,C10orf65","biotype":"protein_coding","ncbi_id":"112817","summary":"The authors of PMID:20797690 cloned this gene while searching for genes in a region of chromosome 10 linked to primary hyperoxalurea type III. They noted that even though the encoded protein has been described as a mitochondrial dihydrodipicolinate synthase-like enzyme, it shares little homology with E. coli dihydrodipicolinate synthase (Dhdps), particularly in the putative substrate-binding region. Moreover, neither lysine biosynthesis nor sialic acid metabolism, for which Dhdps is responsible, occurs in vertebrate mitochondria. They propose that this gene encodes mitochondrial 4-hydroxyl-2-oxoglutarate aldolase (EC 4.1.3.16), which catalyzes the final step in the metabolic pathway of hydroxyproline, releasing glyoxylate and pyruvate. This gene is predominantly expressed in the liver and kidney, and mutations in this gene are found in patients with primary hyperoxalurea type III. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2010]","start":97584323,"end":97612802,"strand":1,"description":"4-hydroxy-2-oxoglutarate aldolase 1 [Source:HGNC Symbol;Acc:HGNC:25155]"}, {"versioned_ensembl_gene_id":"ENSG00000100385.13","gene_symbol":"IL2RB","gene_name":"interleukin 2 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:6009]","synonyms":"IL15RB,CD122","biotype":"protein_coding","ncbi_id":"3560","summary":"The interleukin 2 receptor, which is involved in T cell-mediated immune responses, is present in 3 forms with respect to ability to bind interleukin 2. The low affinity form is a monomer of the alpha subunit and is not involved in signal transduction. The intermediate affinity form consists of an alpha/beta subunit heterodimer, while the high affinity form consists of an alpha/beta/gamma subunit heterotrimer. Both the intermediate and high affinity forms of the receptor are involved in receptor-mediated endocytosis and transduction of mitogenic signals from interleukin 2. The protein encoded by this gene represents the beta subunit and is a type I membrane protein. The use of alternative promoters results in multiple transcript variants encoding the same protein. The protein is primarily expressed in the hematopoietic system. The use by some variants of an alternate promoter in an upstream long terminal repeat (LTR) results in placenta-specific expression. [provided by RefSeq, Sep 2016]","start":37125838,"end":37175054,"strand":-1,"description":"interleukin 2 receptor subunit beta [Source:HGNC Symbol;Acc:HGNC:6009]"}, {"versioned_ensembl_gene_id":"ENSG00000280449.1","gene_symbol":"AC034229.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10168783,"end":10169006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129460.15","gene_symbol":"NGDN","gene_name":"neuroguidin [Source:HGNC Symbol;Acc:HGNC:20271]","synonyms":"NGD,lpd-2,LCP5,DKFZP564O092,CANu1,C14orf120","biotype":"protein_coding","ncbi_id":"25983","summary":"Neuroguidin is an EIF4E (MIM 133440)-binding protein that interacts with CPEB (MIM 607342) and functions as a translational regulatory protein during development of the vertebrate nervous system (Jung et al., 2006 [PubMed 16705177]).[supplied by OMIM, Mar 2008]","start":23469688,"end":23509862,"strand":1,"description":"neuroguidin [Source:HGNC Symbol;Acc:HGNC:20271]"}, {"versioned_ensembl_gene_id":"ENSG00000145192.12","gene_symbol":"AHSG","gene_name":"alpha 2-HS glycoprotein [Source:HGNC Symbol;Acc:HGNC:349]","synonyms":"HSGA,FETUA,A2HS","biotype":"protein_coding","ncbi_id":"197","summary":"The protein encoded by this gene is a negatively-charged serum glycoprotein that is synthesized by hepatocytes. The encoded protein consists of two polypeptide chains, which are both cleaved from a proprotein encoded from a single mRNA. It is involved in several processes, including endocytosis, brain development, and the formation of bone tissue. Defects in this gene are a cause of susceptibility to leanness. [provided by RefSeq, Aug 2017]","start":186612923,"end":186621318,"strand":1,"description":"alpha 2-HS glycoprotein [Source:HGNC Symbol;Acc:HGNC:349]"}, {"versioned_ensembl_gene_id":"ENSG00000273104.1","gene_symbol":"AP000322.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34412200,"end":34412587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140718.20","gene_symbol":"FTO","gene_name":"FTO, alpha-ketoglutarate dependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:24678]","synonyms":"MGC5149,KIAA1752,ALKBH9","biotype":"protein_coding","ncbi_id":"79068","summary":"This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011]","start":53701692,"end":54158512,"strand":1,"description":"FTO, alpha-ketoglutarate dependent dioxygenase [Source:HGNC Symbol;Acc:HGNC:24678]"}, {"versioned_ensembl_gene_id":"ENSG00000142655.12","gene_symbol":"PEX14","gene_name":"peroxisomal biogenesis factor 14 [Source:HGNC Symbol;Acc:HGNC:8856]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5195","summary":"This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome. [provided by RefSeq, Jul 2008]","start":10472288,"end":10630758,"strand":1,"description":"peroxisomal biogenesis factor 14 [Source:HGNC Symbol;Acc:HGNC:8856]"}, {"versioned_ensembl_gene_id":"ENSG00000226003.2","gene_symbol":"AL354714.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":160848010,"end":160848502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243627.4","gene_symbol":"AP000322.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34418715,"end":34423966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152910.18","gene_symbol":"CNTNAP4","gene_name":"contactin associated protein like 4 [Source:HGNC Symbol;Acc:HGNC:18747]","synonyms":"KIAA1763,CASPR4","biotype":"protein_coding","ncbi_id":"85445","summary":"This gene encodes a member of the neurexin protein family. Members of this family function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. This protein may also play a role in proper neurotransmission in the dopaminergic and GABAergic systems and mutations in this gene may be associated with certain psychiatric illnesses. A polymorphism in an intron of this gene may be associated with longevity. [provided by RefSeq, Apr 2016]","start":76277278,"end":76559238,"strand":1,"description":"contactin associated protein like 4 [Source:HGNC Symbol;Acc:HGNC:18747]"}, {"versioned_ensembl_gene_id":"ENSG00000122223.12","gene_symbol":"CD244","gene_name":"CD244 molecule [Source:HGNC Symbol;Acc:HGNC:18171]","synonyms":"NAIL,2B4,SLAMF4,Nmrk,NKR2B4","biotype":"protein_coding","ncbi_id":"51744","summary":"This gene encodes a cell surface receptor expressed on natural killer (NK) cells (and some T cells) that mediate non-major histocompatibility complex (MHC) restricted killing. The interaction between NK-cell and target cells via this receptor is thought to modulate NK-cell cytolytic activity. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":160830160,"end":160862855,"strand":-1,"description":"CD244 molecule [Source:HGNC Symbol;Acc:HGNC:18171]"}, {"versioned_ensembl_gene_id":"ENSG00000272958.1","gene_symbol":"AP000322.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34425508,"end":34426017,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138814.16","gene_symbol":"PPP3CA","gene_name":"protein phosphatase 3 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9314]","synonyms":"PPP2B,CNA1,CALNA,CALN","biotype":"protein_coding","ncbi_id":"5530","summary":null,"start":101023409,"end":101348278,"strand":-1,"description":"protein phosphatase 3 catalytic subunit alpha [Source:HGNC Symbol;Acc:HGNC:9314]"}, {"versioned_ensembl_gene_id":"ENSG00000144120.12","gene_symbol":"TMEM177","gene_name":"transmembrane protein 177 [Source:HGNC Symbol;Acc:HGNC:28143]","synonyms":"MGC10993","biotype":"protein_coding","ncbi_id":"80775","summary":null,"start":119679167,"end":119686507,"strand":1,"description":"transmembrane protein 177 [Source:HGNC Symbol;Acc:HGNC:28143]"}, {"versioned_ensembl_gene_id":"ENSG00000232377.1","gene_symbol":"AC016910.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143937073,"end":143964156,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240163.1","gene_symbol":"AC087385.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60390371,"end":60390682,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118900.14","gene_symbol":"UBN1","gene_name":"ubinuclein 1 [Source:HGNC Symbol;Acc:HGNC:12506]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29855","summary":"Cellular senescence is a hallmark of tumor suppression and tissue aging. Senescent cells contain domains of heterochromatin, called senescence-associated heterochromatin foci (SAHF), that repress proliferation-promoting genes. The protein encoded by this gene binds to proliferation-promoting genes and is required for SAHF formation, enhancing methylation of histone H3. [provided by RefSeq, Oct 2016]","start":4846665,"end":4882360,"strand":1,"description":"ubinuclein 1 [Source:HGNC Symbol;Acc:HGNC:12506]"}, {"versioned_ensembl_gene_id":"ENSG00000121964.14","gene_symbol":"GTDC1","gene_name":"glycosyltransferase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20887]","synonyms":"Hmat-Xa,FLJ11753","biotype":"protein_coding","ncbi_id":"79712","summary":null,"start":143938068,"end":144332568,"strand":-1,"description":"glycosyltransferase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20887]"}, {"versioned_ensembl_gene_id":"ENSG00000225175.1","gene_symbol":"AC109780.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":186687329,"end":186692506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198355.4","gene_symbol":"PIM3","gene_name":"Pim-3 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:19310]","synonyms":null,"biotype":"protein_coding","ncbi_id":"415116","summary":"The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and PIM subfamily. This gene is overexpressed in hematological and epithelial tumors and is associated with MYC coexpression. It plays a role in the regulation of signal transduction cascades, contributing to both cell proliferation and survival, and provides a selective advantage in tumorigenesis. [provided by RefSeq, Jun 2012]","start":49960513,"end":49964080,"strand":1,"description":"Pim-3 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:19310]"}, {"versioned_ensembl_gene_id":"ENSG00000250461.1","gene_symbol":"AC122718.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61375112,"end":61375855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132604.10","gene_symbol":"TERF2","gene_name":"telomeric repeat binding factor 2 [Source:HGNC Symbol;Acc:HGNC:11729]","synonyms":"TRF2,TRBF2","biotype":"protein_coding","ncbi_id":"7014","summary":"This gene encodes a telomere specific protein, TERF2, which is a component of the telomere nucleoprotein complex. This protein is present at telomeres in metaphase of the cell cycle, is a second negative regulator of telomere length and plays a key role in the protective activity of telomeres. While having similar telomere binding activity and domain organization, TERF2 differs from TERF1 in that its N terminus is basic rather than acidic. [provided by RefSeq, Jul 2008]","start":69355561,"end":69408571,"strand":-1,"description":"telomeric repeat binding factor 2 [Source:HGNC Symbol;Acc:HGNC:11729]"}, {"versioned_ensembl_gene_id":"ENSG00000283149.1","gene_symbol":"AC068631.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":186581995,"end":186597103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130449.5","gene_symbol":"ZSWIM6","gene_name":"zinc finger SWIM-type containing 6 [Source:HGNC Symbol;Acc:HGNC:29316]","synonyms":"KIAA1577","biotype":"protein_coding","ncbi_id":"57688","summary":"The protein encoded by this gene contains a zinc finger SWI2/SNF2 and MuDR (SWIM) domain. Proteins with SWIM domains have been found in a diverse number of species and are predicted to interact with DNA or proteins. Mutations in this gene result in acromelic frontonasal dysostosis. [provided by RefSeq, Apr 2017]","start":61332273,"end":61546170,"strand":1,"description":"zinc finger SWIM-type containing 6 [Source:HGNC Symbol;Acc:HGNC:29316]"}, {"versioned_ensembl_gene_id":"ENSG00000230951.1","gene_symbol":"GPS2P2","gene_name":"G protein pathway suppressor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49623]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132058","summary":null,"start":186772589,"end":186773476,"strand":1,"description":"G protein pathway suppressor 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49623]"}, {"versioned_ensembl_gene_id":"ENSG00000113905.4","gene_symbol":"HRG","gene_name":"histidine rich glycoprotein [Source:HGNC Symbol;Acc:HGNC:5181]","synonyms":"HPRG,HRGP","biotype":"protein_coding","ncbi_id":"3273","summary":"This histidine-rich glycoprotein contains two cystatin-like domains and is located in plasma and platelets. The physiological function has not been determined but it is known that the protein binds heme, dyes and divalent metal ions. The encoded protein also has a peptide that displays antimicrobial activity against C. albicans, E. coli, S. aureus, P. aeruginosa, and E. faecalis. It can inhibit rosette formation and interacts with heparin, thrombospondin and plasminogen. Two of the protein's effects, the inhibition of fibrinolysis and the reduction of inhibition of coagulation, indicate a potential prothrombotic effect. Mutations in this gene lead to thrombophilia due to abnormal histidine-rich glycoprotein levels. [provided by RefSeq, Nov 2014]","start":186660216,"end":186678240,"strand":1,"description":"histidine rich glycoprotein [Source:HGNC Symbol;Acc:HGNC:5181]"}, {"versioned_ensembl_gene_id":"ENSG00000139656.6","gene_symbol":"SMIM2","gene_name":"small integral membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:28776]","synonyms":"MGC5590,C13orf44","biotype":"protein_coding","ncbi_id":"79024","summary":null,"start":44143543,"end":44161257,"strand":-1,"description":"small integral membrane protein 2 [Source:HGNC Symbol;Acc:HGNC:28776]"}, {"versioned_ensembl_gene_id":"ENSG00000230731.2","gene_symbol":"AL589745.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44234118,"end":44243192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235285.1","gene_symbol":"SMIM2-IT1","gene_name":"SMIM2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41492]","synonyms":"C13orf44-IT1","biotype":"sense_intronic","ncbi_id":"100874377","summary":null,"start":44146470,"end":44158222,"strand":-1,"description":"SMIM2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41492]"}, {"versioned_ensembl_gene_id":"ENSG00000227258.5","gene_symbol":"SMIM2-AS1","gene_name":"SMIM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42674]","synonyms":"C13orf44-AS1","biotype":"antisense_RNA","ncbi_id":"101929212","summary":null,"start":44110451,"end":44240517,"strand":1,"description":"SMIM2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42674]"}, {"versioned_ensembl_gene_id":"ENSG00000226457.1","gene_symbol":"AL358794.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16369150,"end":16369530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225697.12","gene_symbol":"SLC26A6","gene_name":"solute carrier family 26 member 6 [Source:HGNC Symbol;Acc:HGNC:14472]","synonyms":"DKFZp586E1422","biotype":"protein_coding","ncbi_id":"65010","summary":"This gene belongs to the solute carrier 26 family, whose members encode anion transporter proteins. This particular family member encodes a protein involved in transporting chloride, oxalate, sulfate and bicarbonate. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Aug 2013]","start":48625723,"end":48635493,"strand":-1,"description":"solute carrier family 26 member 6 [Source:HGNC Symbol;Acc:HGNC:14472]"}, {"versioned_ensembl_gene_id":"ENSG00000187144.11","gene_symbol":"SPATA21","gene_name":"spermatogenesis associated 21 [Source:HGNC Symbol;Acc:HGNC:28026]","synonyms":"spergen2,spergen-2","biotype":"protein_coding","ncbi_id":"374955","summary":null,"start":16387117,"end":16437424,"strand":-1,"description":"spermatogenesis associated 21 [Source:HGNC Symbol;Acc:HGNC:28026]"}, {"versioned_ensembl_gene_id":"ENSG00000157399.14","gene_symbol":"ARSE","gene_name":"arylsulfatase E (chondrodysplasia punctata 1) [Source:HGNC Symbol;Acc:HGNC:719]","synonyms":"CDPX,CDPX1","biotype":"protein_coding","ncbi_id":"415","summary":"Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013]","start":2934632,"end":2968310,"strand":-1,"description":"arylsulfatase E (chondrodysplasia punctata 1) [Source:HGNC Symbol;Acc:HGNC:719]"}, {"versioned_ensembl_gene_id":"ENSG00000253352.8","gene_symbol":"TUG1","gene_name":"taurine up-regulated 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26066]","synonyms":"NCRNA00080,LINC00080,FLJ20618","biotype":"antisense_RNA","ncbi_id":"55000","summary":"This gene produces a long non-coding RNA that interacts with the Polycomb repressor complex and functions in the epigenetic regulation of transcription. This RNA promotes cell proliferation and is upregulated in tumor cells. It may act as a sponge for microRNAs. The homologous mouse gene is required for differentiation of retina. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2017]","start":30970677,"end":30979395,"strand":1,"description":"taurine up-regulated 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26066]"}, {"versioned_ensembl_gene_id":"ENSG00000177181.14","gene_symbol":"RIMKLA","gene_name":"ribosomal modification protein rimK like family member A [Source:HGNC Symbol;Acc:HGNC:28725]","synonyms":"RP11-157D18.1,NAAGS-II,MGC47816,FAM80A","biotype":"protein_coding","ncbi_id":"284716","summary":null,"start":42380795,"end":42422578,"strand":1,"description":"ribosomal modification protein rimK like family member A [Source:HGNC Symbol;Acc:HGNC:28725]"}, {"versioned_ensembl_gene_id":"ENSG00000129159.7","gene_symbol":"KCNC1","gene_name":"potassium voltage-gated channel subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:6233]","synonyms":"Kv3.1","biotype":"protein_coding","ncbi_id":"3746","summary":"This gene encodes a member of a family of integral membrane proteins that mediate the voltage-dependent potassium ion permeability of excitable membranes. Alternative splicing is thought to result in two transcript variants encoding isoforms that differ at their C-termini. These isoforms have had conflicting names in the literature: the longer isoform has been called both \"b\" and \"alpha\", while the shorter isoform has been called both \"a\" and \"beta\" (PMIDs 1432046, 12091563). [provided by RefSeq, Oct 2014]","start":17734774,"end":17856804,"strand":1,"description":"potassium voltage-gated channel subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:6233]"}, {"versioned_ensembl_gene_id":"ENSG00000046604.12","gene_symbol":"DSG2","gene_name":"desmoglein 2 [Source:HGNC Symbol;Acc:HGNC:3049]","synonyms":"CDHF5","biotype":"protein_coding","ncbi_id":"1829","summary":"This gene encodes a member of the desmoglein family and cadherin cell adhesion molecule superfamily of proteins. Desmogleins are calcium-binding transmembrane glycoprotein components of desmosomes, cell-cell junctions between epithelial, myocardial, and other cell types. The encoded preproprotein is proteolytically processed to generate the mature glycoprotein. This gene is present in a gene cluster with other desmoglein gene family members on chromosome 18. Mutations in this gene have been associated with arrhythmogenic right ventricular dysplasia, familial, 10. [provided by RefSeq, Jan 2016]","start":31498043,"end":31549008,"strand":1,"description":"desmoglein 2 [Source:HGNC Symbol;Acc:HGNC:3049]"}, {"versioned_ensembl_gene_id":"ENSG00000182722.5","gene_symbol":"SEPHS1P1","gene_name":"selenophosphate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42161]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"168474","summary":null,"start":64852397,"end":64853354,"strand":-1,"description":"selenophosphate synthetase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42161]"}, {"versioned_ensembl_gene_id":"ENSG00000213891.3","gene_symbol":"RPL3P6","gene_name":"ribosomal protein L3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36395]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643220","summary":null,"start":61390668,"end":61391871,"strand":-1,"description":"ribosomal protein L3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36395]"}, {"versioned_ensembl_gene_id":"ENSG00000278496.1","gene_symbol":"AL158062.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27077218,"end":27077962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262628.1","gene_symbol":"OR1D5","gene_name":"olfactory receptor family 1 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:8186]","synonyms":"OR17-31","biotype":"protein_coding","ncbi_id":"8386","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3062669,"end":3063607,"strand":-1,"description":"olfactory receptor family 1 subfamily D member 5 [Source:HGNC Symbol;Acc:HGNC:8186]"}, {"versioned_ensembl_gene_id":"ENSG00000251682.1","gene_symbol":"AC122718.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61347126,"end":61347716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152484.13","gene_symbol":"USP12","gene_name":"ubiquitin specific peptidase 12 [Source:HGNC Symbol;Acc:HGNC:20485]","synonyms":"USP12L1","biotype":"protein_coding","ncbi_id":"219333","summary":null,"start":27066142,"end":27171896,"strand":-1,"description":"ubiquitin specific peptidase 12 [Source:HGNC Symbol;Acc:HGNC:20485]"}, {"versioned_ensembl_gene_id":"ENSG00000228004.1","gene_symbol":"MYCLP2","gene_name":"MYCL pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645136","summary":null,"start":57933837,"end":57934803,"strand":-1,"description":"MYCL pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:48924]"}, {"versioned_ensembl_gene_id":"ENSG00000279498.1","gene_symbol":"AL356121.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108359084,"end":108359863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226519.1","gene_symbol":"LINC00390","gene_name":"long intergenic non-protein coding RNA 390 [Source:HGNC Symbol;Acc:HGNC:42718]","synonyms":"TCONS_00021641","biotype":"lincRNA","ncbi_id":"105370183","summary":null,"start":44106378,"end":44137236,"strand":-1,"description":"long intergenic non-protein coding RNA 390 [Source:HGNC Symbol;Acc:HGNC:42718]"}, {"versioned_ensembl_gene_id":"ENSG00000213640.3","gene_symbol":"EEF1DP4","gene_name":"eukaryotic translation elongation factor 1 delta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:22598]","synonyms":"FLJ26697","biotype":"processed_pseudogene","ncbi_id":"442325","summary":null,"start":64862999,"end":64864370,"strand":1,"description":"eukaryotic translation elongation factor 1 delta pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:22598]"}, {"versioned_ensembl_gene_id":"ENSG00000232687.1","gene_symbol":"RPL12P9","gene_name":"ribosomal protein L12 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23766]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"654376","summary":null,"start":29127701,"end":29128188,"strand":-1,"description":"ribosomal protein L12 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:23766]"}, {"versioned_ensembl_gene_id":"ENSG00000276854.1","gene_symbol":"AL589745.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44196006,"end":44197298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235124.1","gene_symbol":"KRT8P17","gene_name":"keratin 8 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:33369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392479","summary":null,"start":57984686,"end":57986133,"strand":1,"description":"keratin 8 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:33369]"}, {"versioned_ensembl_gene_id":"ENSG00000171388.11","gene_symbol":"APLN","gene_name":"apelin [Source:HGNC Symbol;Acc:HGNC:16665]","synonyms":"XNPEP2,apelin","biotype":"protein_coding","ncbi_id":"8862","summary":"This gene encodes a peptide that functions as an endogenous ligand for the G-protein coupled apelin receptor. The encoded preproprotein is proteolytically processed into biologically active C-terminal peptide fragments. These peptide fragments activate different tissue specific signaling pathways that regulate diverse biological functions including fluid homeostasis, cardiovascular function and insulin secretion. This protein also functions as a coreceptor for the human immunodeficiency virus 1. [provided by RefSeq, Feb 2016]","start":129645259,"end":129654937,"strand":-1,"description":"apelin [Source:HGNC Symbol;Acc:HGNC:16665]"}, {"versioned_ensembl_gene_id":"ENSG00000122375.11","gene_symbol":"OPN4","gene_name":"opsin 4 [Source:HGNC Symbol;Acc:HGNC:14449]","synonyms":"MOP,melanopsin","biotype":"protein_coding","ncbi_id":"94233","summary":"Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This gene encodes a photoreceptive opsin protein that is expressed within the ganglion and amacrine cell layers of the retina. In mouse, retinal ganglion cell axons expressing this gene projected to the suprachiasmatic nucleus and other brain nuclei involved in circadian photoentrainment. In mouse, this protein is coupled to a transient receptor potential (TRP) ion channel through a G protein signaling pathway and produces a physiologic light response via membrane depolarization and increased intracellular calcium. The protein functions as a sensory photopigment and may also have photoisomerase activity. Experiments with knockout mice indicate that this gene attenuates, but does not abolish, photoentrainment. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":86654557,"end":86666848,"strand":1,"description":"opsin 4 [Source:HGNC Symbol;Acc:HGNC:14449]"}, {"versioned_ensembl_gene_id":"ENSG00000092345.13","gene_symbol":"DAZL","gene_name":"deleted in azoospermia like [Source:HGNC Symbol;Acc:HGNC:2685]","synonyms":"SPGYLA,MGC26406,DAZLA,DAZL1,DAZH","biotype":"protein_coding","ncbi_id":"1618","summary":"The DAZ (Deleted in AZoospermia) gene family encodes potential RNA binding proteins that are expressed in prenatal and postnatal germ cells of males and females. The protein encoded by this gene is localized to the nucleus and cytoplasm of fetal germ cells and to the cytoplasm of developing oocytes. In the testis, this protein is localized to the nucleus of spermatogonia but relocates to the cytoplasm during meiosis where it persists in spermatids and spermatozoa. Transposition and amplification of this autosomal gene during primate evolution gave rise to the DAZ gene cluster on the Y chromosome. Mutations in this gene have been linked to severe spermatogenic failure and infertility in males. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":16586792,"end":16670306,"strand":-1,"description":"deleted in azoospermia like [Source:HGNC Symbol;Acc:HGNC:2685]"}, {"versioned_ensembl_gene_id":"ENSG00000271370.1","gene_symbol":"AC007619.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12452103,"end":12452481,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198467.13","gene_symbol":"TPM2","gene_name":"tropomyosin 2 [Source:HGNC Symbol;Acc:HGNC:12011]","synonyms":"NEM4,DA1,AMCD1","biotype":"protein_coding","ncbi_id":"7169","summary":"This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]","start":35681992,"end":35691020,"strand":-1,"description":"tropomyosin 2 [Source:HGNC Symbol;Acc:HGNC:12011]"}, {"versioned_ensembl_gene_id":"ENSG00000122121.10","gene_symbol":"XPNPEP2","gene_name":"X-prolyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:12823]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7512","summary":"Aminopeptidase P is a hydrolase specific for N-terminal imido bonds, which are common to several collagen degradation products, neuropeptides, vasoactive peptides, and cytokines. Structurally, the enzyme is a member of the 'pita bread fold' family and occurs in mammalian tissues in both soluble and GPI-anchored membrane-bound forms. A membrane-bound and soluble form of this enzyme have been identified as products of two separate genes. [provided by RefSeq, Jul 2008]","start":129738974,"end":129769538,"strand":1,"description":"X-prolyl aminopeptidase 2 [Source:HGNC Symbol;Acc:HGNC:12823]"}, {"versioned_ensembl_gene_id":"ENSG00000269972.1","gene_symbol":"AC004542.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30977516,"end":30977858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269987.1","gene_symbol":"AC004542.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30976515,"end":30978848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236852.1","gene_symbol":"BX322784.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62779250,"end":62780326,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278154.4","gene_symbol":"LAIR1","gene_name":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]","synonyms":"CD305","biotype":"protein_coding","ncbi_id":"3903","summary":"The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":54361220,"end":54378234,"strand":-1,"description":"leukocyte associated immunoglobulin like receptor 1 [Source:HGNC Symbol;Acc:HGNC:6477]"}, {"versioned_ensembl_gene_id":"ENSG00000235170.1","gene_symbol":"MTND1P31","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42080]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873217","summary":null,"start":62842542,"end":62843502,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42080]"}, {"versioned_ensembl_gene_id":"ENSG00000129167.9","gene_symbol":"TPH1","gene_name":"tryptophan hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:12008]","synonyms":"TPRH,TPH","biotype":"protein_coding","ncbi_id":"7166","summary":"This gene encodes a member of the aromatic amino acid hydroxylase family. The encoded protein catalyzes the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. Mutations in this gene have been associated with an elevated risk for a variety of diseases and disorders, including schizophrenia, somatic anxiety, anger-related traits, bipolar disorder, suicidal behavior, addictions, and others.[provided by RefSeq, Apr 2009]","start":18017564,"end":18042426,"strand":-1,"description":"tryptophan hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:12008]"}, {"versioned_ensembl_gene_id":"ENSG00000229211.3","gene_symbol":"KCTD9P6","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642513","summary":null,"start":31219894,"end":31220984,"strand":-1,"description":"potassium channel tetramerization domain containing 9 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49915]"}, {"versioned_ensembl_gene_id":"ENSG00000055070.16","gene_symbol":"SZRD1","gene_name":"SUZ RNA binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30232]","synonyms":"DKFZp566C0424,C1orf144","biotype":"protein_coding","ncbi_id":"26099","summary":null,"start":16352575,"end":16398145,"strand":1,"description":"SUZ RNA binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30232]"}, {"versioned_ensembl_gene_id":"ENSG00000254095.1","gene_symbol":"AC068672.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":31339197,"end":31346479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253377.1","gene_symbol":"AC068672.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31275596,"end":31384279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198039.11","gene_symbol":"ZNF273","gene_name":"zinc finger protein 273 [Source:HGNC Symbol;Acc:HGNC:13067]","synonyms":"HZF9","biotype":"protein_coding","ncbi_id":"10793","summary":"This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with 13 C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in transcriptional regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":64870172,"end":64930966,"strand":1,"description":"zinc finger protein 273 [Source:HGNC Symbol;Acc:HGNC:13067]"}, {"versioned_ensembl_gene_id":"ENSG00000102003.10","gene_symbol":"SYP","gene_name":"synaptophysin [Source:HGNC Symbol;Acc:HGNC:11506]","synonyms":"MRX96","biotype":"protein_coding","ncbi_id":"6855","summary":"This gene encodes an integral membrane protein of small synaptic vesicles in brain and endocrine cells. The protein also binds cholesterol and is thought to direct targeting of vesicle-associated membrane protein 2 (synaptobrevin) to intracellular compartments. Mutations in this gene are associated with an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017]","start":49187804,"end":49200259,"strand":-1,"description":"synaptophysin [Source:HGNC Symbol;Acc:HGNC:11506]"}, {"versioned_ensembl_gene_id":"ENSG00000271970.1","gene_symbol":"AL355802.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43561872,"end":43562419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264859.5","gene_symbol":"DSG2-AS1","gene_name":"DSG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51311]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652770","summary":null,"start":31542146,"end":31556911,"strand":-1,"description":"DSG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51311]"}, {"versioned_ensembl_gene_id":"ENSG00000137207.11","gene_symbol":"YIPF3","gene_name":"Yip1 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:21023]","synonyms":"KLIP1,FinGER3,DKFZp566C243,dJ337H4.3,C6orf109","biotype":"protein_coding","ncbi_id":"25844","summary":null,"start":43511827,"end":43516990,"strand":-1,"description":"Yip1 domain family member 3 [Source:HGNC Symbol;Acc:HGNC:21023]"}, {"versioned_ensembl_gene_id":"ENSG00000232162.1","gene_symbol":"USP12-AS1","gene_name":"USP12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39961]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874070","summary":null,"start":27162855,"end":27169135,"strand":1,"description":"USP12 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39961]"}, {"versioned_ensembl_gene_id":"ENSG00000264964.1","gene_symbol":"AP001033.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9315194,"end":9334441,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168802.12","gene_symbol":"CHTF8","gene_name":"chromosome transmission fidelity factor 8 [Source:HGNC Symbol;Acc:HGNC:24353]","synonyms":"FLJ20400,DERPC,CTF8","biotype":"protein_coding","ncbi_id":"54921","summary":"This gene encodes a short protein that forms part of the Ctf18 replication factor C (RFC) complex that occurs in both yeast and mammals. The heteroheptameric RFC complex plays a role in sister chromatid cohesion and may load the replication clamp PCNA (proliferating cell nuclear antigen) onto DNA during DNA replication and repair. This gene is ubiquitously expressed and has been shown to have reduced expression in renal and prostate tumors. Alternatively spliced transcript variants have been described. This gene has a pseudogene on chromosome X. [provided by RefSeq, Oct 2018]","start":69118010,"end":69132584,"strand":-1,"description":"chromosome transmission fidelity factor 8 [Source:HGNC Symbol;Acc:HGNC:24353]"}, {"versioned_ensembl_gene_id":"ENSG00000257740.1","gene_symbol":"AC073896.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56308868,"end":56309449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144785.8","gene_symbol":"AC073896.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":56285916,"end":56316059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205667.2","gene_symbol":"ARSH","gene_name":"arylsulfatase family member H [Source:HGNC Symbol;Acc:HGNC:32488]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347527","summary":"Sulfatases, such as ARSH, hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules (Sardiello et al., 2005 [PubMed 16174644]).[supplied by OMIM, Mar 2008]","start":3006613,"end":3033571,"strand":1,"description":"arylsulfatase family member H [Source:HGNC Symbol;Acc:HGNC:32488]"}, {"versioned_ensembl_gene_id":"ENSG00000227315.7","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31845195,"end":31850443,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000136982.5","gene_symbol":"DSCC1","gene_name":"DNA replication and sister chromatid cohesion 1 [Source:HGNC Symbol;Acc:HGNC:24453]","synonyms":"MGC5528,hDCC1,DCC1","biotype":"protein_coding","ncbi_id":"79075","summary":"CHTF18 (MIM 613201), CHTF8 (MIM 613202), and DSCC1 are components of an alternative replication factor C (RFC) (see MIM 600404) complex that loads PCNA (MIM 176740) onto DNA during S phase of the cell cycle (Merkle et al., 2003 [PubMed 12766176]; Bermudez et al., 2003 [PubMed 12930902]).[supplied by OMIM, Dec 2009]","start":119833976,"end":119856010,"strand":-1,"description":"DNA replication and sister chromatid cohesion 1 [Source:HGNC Symbol;Acc:HGNC:24453]"}, {"versioned_ensembl_gene_id":"ENSG00000228182.1","gene_symbol":"MTND2P25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42126]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873231","summary":null,"start":62843697,"end":62844306,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42126]"}, {"versioned_ensembl_gene_id":"ENSG00000234570.1","gene_symbol":"ZFRP1","gene_name":"zinc finger RNA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38030]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129438","summary":null,"start":62878811,"end":62884842,"strand":-1,"description":"zinc finger RNA binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38030]"}, {"versioned_ensembl_gene_id":"ENSG00000221968.8","gene_symbol":"FADS3","gene_name":"fatty acid desaturase 3 [Source:HGNC Symbol;Acc:HGNC:3576]","synonyms":"LLCDL3,CYB5RP","biotype":"protein_coding","ncbi_id":"3995","summary":"The protein encoded by this gene is a member of the fatty acid desaturase (FADS) gene family. Desaturase enzymes regulate unsaturation of fatty acids through the introduction of double bonds between defined carbons of the fatty acyl chain. FADS family members are considered fusion products composed of an N-terminal cytochrome b5-like domain and a C-terminal multiple membrane-spanning desaturase portion, both of which are characterized by conserved histidine motifs. This gene is clustered with family members FADS1 and FADS2 at 11q12-q13.1; this cluster is thought to have arisen evolutionarily from gene duplication based on its similar exon/intron organization. [provided by RefSeq, Jul 2008]","start":61873519,"end":61892051,"strand":-1,"description":"fatty acid desaturase 3 [Source:HGNC Symbol;Acc:HGNC:3576]"}, {"versioned_ensembl_gene_id":"ENSG00000277499.1","gene_symbol":"AL359854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63087071,"end":63088664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230823.3","gene_symbol":"CBX1P1","gene_name":"chromobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38655]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645251","summary":null,"start":63299247,"end":63299673,"strand":-1,"description":"chromobox 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38655]"}, {"versioned_ensembl_gene_id":"ENSG00000117601.13","gene_symbol":"SERPINC1","gene_name":"serpin family C member 1 [Source:HGNC Symbol;Acc:HGNC:775]","synonyms":"MGC22579,ATIII,AT3","biotype":"protein_coding","ncbi_id":"462","summary":"The protein encoded by this gene, antithrombin III, is a plasma protease inhibitor and a member of the serpin superfamily. This protein inhibits thrombin as well as other activated serine proteases of the coagulation system, and it regulates the blood coagulation cascade. The protein includes two functional domains: the heparin binding-domain at the N-terminus of the mature protein, and the reactive site domain at the C-terminus. The inhibitory activity is enhanced by the presence of heparin. Numerous mutations have been identified for this gene, many of which are known to cause antithrombin-III deficiency which constitutes a strong risk factor for thrombosis. A reduction in the serum level of this protein is associated with severe cases of Coronavirus Disease 19 (COVID-19). [provided by RefSeq, Sep 2020]","start":173903804,"end":173917378,"strand":-1,"description":"serpin family C member 1 [Source:HGNC Symbol;Acc:HGNC:775]"}, {"versioned_ensembl_gene_id":"ENSG00000128791.11","gene_symbol":"TWSG1","gene_name":"twisted gastrulation BMP signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:12429]","synonyms":"TSG","biotype":"protein_coding","ncbi_id":"57045","summary":null,"start":9334767,"end":9402420,"strand":1,"description":"twisted gastrulation BMP signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:12429]"}, {"versioned_ensembl_gene_id":"ENSG00000115194.10","gene_symbol":"SLC30A3","gene_name":"solute carrier family 30 member 3 [Source:HGNC Symbol;Acc:HGNC:11014]","synonyms":"ZNT3","biotype":"protein_coding","ncbi_id":"7781","summary":null,"start":27253684,"end":27275817,"strand":-1,"description":"solute carrier family 30 member 3 [Source:HGNC Symbol;Acc:HGNC:11014]"}, {"versioned_ensembl_gene_id":"ENSG00000255448.1","gene_symbol":"AC055860.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18000542,"end":18022931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257727.5","gene_symbol":"CNPY2","gene_name":"canopy FGF signaling regulator 2 [Source:HGNC Symbol;Acc:HGNC:13529]","synonyms":"ZSIG9,TMEM4,HP10390,Cnpy2","biotype":"protein_coding","ncbi_id":"10330","summary":null,"start":56309842,"end":56316336,"strand":-1,"description":"canopy FGF signaling regulator 2 [Source:HGNC Symbol;Acc:HGNC:13529]"}, {"versioned_ensembl_gene_id":"ENSG00000279347.1","gene_symbol":"AC021945.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":119838736,"end":119840385,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238199.1","gene_symbol":"UBE2V2P3","gene_name":"ubiquitin conjugating enzyme E2 V2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44891]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421341","summary":null,"start":11278616,"end":11279351,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44891]"}, {"versioned_ensembl_gene_id":"ENSG00000281524.1","gene_symbol":"AC139749.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1061530,"end":1067399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137802.13","gene_symbol":"MAPKBP1","gene_name":"mitogen-activated protein kinase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29536]","synonyms":"KIAA0596","biotype":"protein_coding","ncbi_id":"23005","summary":"This gene encodes a scaffold protein that regulates the JNK (c-Jun N-terminal kinase) and NOD2 (nucleotide-binding oligomerization domain-containing protein 2) signaling pathways. The encoded protein interacts with another related JNK pathway scaffold protein, WDR62, via a conserved dimerization domain, and enhances JNK signaling. This protein may play a role in bacterial immunity by binding to the NOD2 receptor and negatively regulating downstream antibacterial and pro-inflammatory signaling. Mutations in this gene that impair cellular localization of the encoded protein cause a form of nephronophthisis, an autosomal-recessive kidney disorder, in human patients. [provided by RefSeq, May 2017]","start":41774434,"end":41827855,"strand":1,"description":"mitogen-activated protein kinase binding protein 1 [Source:HGNC Symbol;Acc:HGNC:29536]"}, {"versioned_ensembl_gene_id":"ENSG00000120942.13","gene_symbol":"UBIAD1","gene_name":"UbiA prenyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30791]","synonyms":"TERE1,SCCD","biotype":"protein_coding","ncbi_id":"29914","summary":"This gene encodes a protein thought to be involved in cholesterol and phospholipid metabolism. Mutations in this gene are associated with Schnyder crystalline corneal dystrophy. [provided by RefSeq, Oct 2008]","start":11273206,"end":11296049,"strand":1,"description":"UbiA prenyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30791]"}, {"versioned_ensembl_gene_id":"ENSG00000228451.3","gene_symbol":"SDAD1P1","gene_name":"SDA1 domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31403]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"157489","summary":null,"start":26379259,"end":26382953,"strand":-1,"description":"SDA1 domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31403]"}, {"versioned_ensembl_gene_id":"ENSG00000129158.10","gene_symbol":"SERGEF","gene_name":"secretion regulating guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:17499]","synonyms":"DelGEF,Gnefr","biotype":"protein_coding","ncbi_id":"26297","summary":null,"start":17788048,"end":18013162,"strand":-1,"description":"secretion regulating guanine nucleotide exchange factor [Source:HGNC Symbol;Acc:HGNC:17499]"}, {"versioned_ensembl_gene_id":"ENSG00000277831.1","gene_symbol":"AL138960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44369365,"end":44369877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237341.1","gene_symbol":"SYP-AS1","gene_name":"SYP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40571]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873921","summary":null,"start":49198966,"end":49202454,"strand":1,"description":"SYP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40571]"}, {"versioned_ensembl_gene_id":"ENSG00000111266.8","gene_symbol":"DUSP16","gene_name":"dual specificity phosphatase 16 [Source:HGNC Symbol;Acc:HGNC:17909]","synonyms":"MKP7,MKP-7,KIAA1700","biotype":"protein_coding","ncbi_id":"80824","summary":"This gene encodes a mitogen-activated protein kinase phosphatase that is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. The encoded protein specifically regulates the c-Jun amino-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) pathways.[provided by RefSeq, May 2010]","start":12474210,"end":12562383,"strand":-1,"description":"dual specificity phosphatase 16 [Source:HGNC Symbol;Acc:HGNC:17909]"}, {"versioned_ensembl_gene_id":"ENSG00000253430.1","gene_symbol":"AC011726.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26422593,"end":26423929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240694.8","gene_symbol":"PNMA2","gene_name":"paraneoplastic Ma antigen 2 [Source:HGNC Symbol;Acc:HGNC:9159]","synonyms":"RGAG2,MA2","biotype":"protein_coding","ncbi_id":"10687","summary":null,"start":26504686,"end":26514092,"strand":-1,"description":"paraneoplastic Ma antigen 2 [Source:HGNC Symbol;Acc:HGNC:9159]"}, {"versioned_ensembl_gene_id":"ENSG00000151778.10","gene_symbol":"SERP2","gene_name":"stress associated endoplasmic reticulum protein family member 2 [Source:HGNC Symbol;Acc:HGNC:20607]","synonyms":"C13orf21,bA269C23.1","biotype":"protein_coding","ncbi_id":"387923","summary":null,"start":44373665,"end":44397714,"strand":1,"description":"stress associated endoplasmic reticulum protein family member 2 [Source:HGNC Symbol;Acc:HGNC:20607]"}, {"versioned_ensembl_gene_id":"ENSG00000228527.1","gene_symbol":"AC016396.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58304553,"end":58305621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261076.1","gene_symbol":"AC016396.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58325614,"end":58327030,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246526.2","gene_symbol":"LINC002481","gene_name":"long intergenic non-protein coding RNA 2481 [Source:HGNC Symbol;Acc:HGNC:27958]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339988","summary":null,"start":6687448,"end":6690519,"strand":-1,"description":"long intergenic non-protein coding RNA 2481 [Source:HGNC Symbol;Acc:HGNC:27958]"}, {"versioned_ensembl_gene_id":"ENSG00000233180.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR2B3P,OR6-4","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29082970,"end":29083976,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000062096.14","gene_symbol":"ARSF","gene_name":"arylsulfatase F [Source:HGNC Symbol;Acc:HGNC:721]","synonyms":null,"biotype":"protein_coding","ncbi_id":"416","summary":"This gene is a member of the sulfatase family, and more specifically, the arylsulfatase subfamily. Members of the subfamily share similarity in sequence and splice sites, and are clustered together on chromosome X, suggesting that they are derived from recent gene duplication events. Sulfatases are essential for the correct composition of bone and cartilage matrix. The activity of this protein, unlike that of arylsulfatase E, is not inhibited by warfarin. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jan 2011]","start":3041471,"end":3112726,"strand":1,"description":"arylsulfatase F [Source:HGNC Symbol;Acc:HGNC:721]"}, {"versioned_ensembl_gene_id":"ENSG00000224039.1","gene_symbol":"CDYLP1","gene_name":"chromodomain Y-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52805]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132260","summary":null,"start":16692745,"end":16694202,"strand":-1,"description":"chromodomain Y-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52805]"}, {"versioned_ensembl_gene_id":"ENSG00000263150.3","gene_symbol":"OR8J2","gene_name":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]","synonyms":"OR8J2P","biotype":"polymorphic_pseudogene","ncbi_id":"81169","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56210873,"end":56211820,"strand":-1,"description":"olfactory receptor family 8 subfamily J member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15311]"}, {"versioned_ensembl_gene_id":"ENSG00000229271.1","gene_symbol":"AC091493.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16687986,"end":16697479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284646.1","gene_symbol":"AL031291.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11311734,"end":11319093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279859.2","gene_symbol":"AC093323.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6691995,"end":6692970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262851.2","gene_symbol":"OR5T2","gene_name":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219464","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56232106,"end":56233185,"strand":-1,"description":"olfactory receptor family 5 subfamily T member 2 [Source:HGNC Symbol;Acc:HGNC:15296]"}, {"versioned_ensembl_gene_id":"ENSG00000222038.3","gene_symbol":"POTEJ","gene_name":"POTE ankyrin domain family member J [Source:HGNC Symbol;Acc:HGNC:37094]","synonyms":"POTE2beta","biotype":"protein_coding","ncbi_id":"653781","summary":null,"start":130611481,"end":130658091,"strand":1,"description":"POTE ankyrin domain family member J [Source:HGNC Symbol;Acc:HGNC:37094]"}, {"versioned_ensembl_gene_id":"ENSG00000277647.1","gene_symbol":"AC126755.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18357026,"end":18357136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164111.14","gene_symbol":"ANXA5","gene_name":"annexin A5 [Source:HGNC Symbol;Acc:HGNC:543]","synonyms":"ENX2,ANX5","biotype":"protein_coding","ncbi_id":"308","summary":"The Annexin 5 gene spans 29 kb containing 13 exons, and encodes a single transcript of approximately 1.6 kb and a protein product with a molecular weight of about 35 kDa.The protein encoded by this gene belongs to the annexin family of calcium-dependent phospholipid binding proteins some of which have been implicated in membrane-related events along exocytotic and endocytotic pathways. Annexin 5 is a phospholipase A2 and protein kinase C inhibitory protein with calcium channel activity and a potential role in cellular signal transduction, inflammation, growth and differentiation. Annexin 5 has also been described as placental anticoagulant protein I, vascular anticoagulant-alpha, endonexin II, lipocortin V, placental protein 4 and anchorin CII. Polymorphisms in this gene have been implicated in various obstetric complications. [provided by RefSeq, Dec 2019]","start":121667955,"end":121697113,"strand":-1,"description":"annexin A5 [Source:HGNC Symbol;Acc:HGNC:543]"}, {"versioned_ensembl_gene_id":"ENSG00000255302.4","gene_symbol":"EID1","gene_name":"EP300 interacting inhibitor of differentiation 1 [Source:HGNC Symbol;Acc:HGNC:1191]","synonyms":"C15orf3,EID-1,CRI1","biotype":"protein_coding","ncbi_id":"23741","summary":null,"start":48877886,"end":48880183,"strand":1,"description":"EP300 interacting inhibitor of differentiation 1 [Source:HGNC Symbol;Acc:HGNC:1191]"}, {"versioned_ensembl_gene_id":"ENSG00000135090.13","gene_symbol":"TAOK3","gene_name":"TAO kinase 3 [Source:HGNC Symbol;Acc:HGNC:18133]","synonyms":"MAP3K18,JIK,DPK","biotype":"protein_coding","ncbi_id":"51347","summary":"The protein encoded by this gene is a serine/threonine protein kinase that activates the p38/MAPK14 stress-activated MAPK cascade but inhibits the basal activity of the MAPK8/JNK cascade. The encoded protein is a member of the GCK subfamily of STE20-like kinases. [provided by RefSeq, Oct 2016]","start":118149801,"end":118372945,"strand":-1,"description":"TAO kinase 3 [Source:HGNC Symbol;Acc:HGNC:18133]"}, {"versioned_ensembl_gene_id":"ENSG00000180509.11","gene_symbol":"KCNE1","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:6240]","synonyms":"JLNS2,ISK,minK,LQT5","biotype":"protein_coding","ncbi_id":"3753","summary":"The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":34446688,"end":34512275,"strand":-1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:6240]"}, {"versioned_ensembl_gene_id":"ENSG00000259602.1","gene_symbol":"AC091073.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48938236,"end":48948031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185634.11","gene_symbol":"SHC4","gene_name":"SHC adaptor protein 4 [Source:HGNC Symbol;Acc:HGNC:16743]","synonyms":"SHCD,RaLP","biotype":"protein_coding","ncbi_id":"399694","summary":null,"start":48823735,"end":48963444,"strand":-1,"description":"SHC adaptor protein 4 [Source:HGNC Symbol;Acc:HGNC:16743]"}, {"versioned_ensembl_gene_id":"ENSG00000174915.11","gene_symbol":"PTDSS2","gene_name":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]","synonyms":"PSS2","biotype":"protein_coding","ncbi_id":"81490","summary":"The protein encoded by this gene catalyzes the conversion of phosphatidylethanolamine to phosphatidylserine, a structural membrane phospholipid that functions in cell signaling, blood coagulation, and apoptosis. The encoded enzyme also has a high affinity for docosahexaenoic acid (DHA) and can use it to make DHA-containing phosphatidylserine. [provided by RefSeq, Jul 2016]","start":448268,"end":491399,"strand":1,"description":"phosphatidylserine synthase 2 [Source:HGNC Symbol;Acc:HGNC:15463]"}, {"versioned_ensembl_gene_id":"ENSG00000280098.1","gene_symbol":"AC011155.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":52409042,"end":52409257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265113.1","gene_symbol":"AC026474.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":69240549,"end":69241929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273762.1","gene_symbol":"AC011155.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52419189,"end":52419644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162191.13","gene_symbol":"UBXN1","gene_name":"UBX domain protein 1 [Source:HGNC Symbol;Acc:HGNC:18402]","synonyms":"2B28,UBXD10,SAKS1,LOC51035","biotype":"protein_coding","ncbi_id":"51035","summary":null,"start":62676498,"end":62679117,"strand":-1,"description":"UBX domain protein 1 [Source:HGNC Symbol;Acc:HGNC:18402]"}, {"versioned_ensembl_gene_id":"ENSG00000272617.2","gene_symbol":"COG8","gene_name":"component of oligomeric golgi complex 8 [Source:HGNC Symbol;Acc:HGNC:18623]","synonyms":"DOR1,FLJ22315,DOR1,FLJ22315","biotype":"protein_coding","ncbi_id":"84342","summary":"This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]","start":69326913,"end":69339667,"strand":-1,"description":"component of oligomeric golgi complex 8 [Source:HGNC Symbol;Acc:HGNC:18623]"}, {"versioned_ensembl_gene_id":"ENSG00000264263.1","gene_symbol":"AC103949.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53480835,"end":53568283,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229700.1","gene_symbol":"AL008627.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20042455,"end":20042940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251203.1","gene_symbol":"AC011726.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26433029,"end":26434065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255670.1","gene_symbol":"AC007619.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12485353,"end":12491581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104765.15","gene_symbol":"BNIP3L","gene_name":"BCL2 interacting protein 3 like [Source:HGNC Symbol;Acc:HGNC:1085]","synonyms":"Nix,BNIP3a","biotype":"protein_coding","ncbi_id":"665","summary":"This gene encodes a protein that belongs to the pro-apoptotic subfamily within the Bcl-2 family of proteins. The encoded protein binds to Bcl-2 and possesses the BH3 domain. The protein directly targets mitochondria and causes apoptotic changes, including loss of membrane potential and the release of cytochrome c. [provided by RefSeq, Feb 2015]","start":26382898,"end":26505636,"strand":1,"description":"BCL2 interacting protein 3 like [Source:HGNC Symbol;Acc:HGNC:1085]"}, {"versioned_ensembl_gene_id":"ENSG00000188263.10","gene_symbol":"IL17REL","gene_name":"interleukin 17 receptor E like [Source:HGNC Symbol;Acc:HGNC:33808]","synonyms":"FLJ41993","biotype":"protein_coding","ncbi_id":"400935","summary":null,"start":49994513,"end":50012659,"strand":-1,"description":"interleukin 17 receptor E like [Source:HGNC Symbol;Acc:HGNC:33808]"}, {"versioned_ensembl_gene_id":"ENSG00000187323.11","gene_symbol":"DCC","gene_name":"DCC netrin 1 receptor [Source:HGNC Symbol;Acc:HGNC:2701]","synonyms":"NTN1R1,IGDCC1","biotype":"protein_coding","ncbi_id":"1630","summary":"This gene encodes a netrin 1 receptor. The transmembrane protein is a member of the immunoglobulin superfamily of cell adhesion molecules, and mediates axon guidance of neuronal growth cones towards sources of netrin 1 ligand. The cytoplasmic tail interacts with the tyrosine kinases Src and focal adhesion kinase (FAK, also known as PTK2) to mediate axon attraction. The protein partially localizes to lipid rafts, and induces apoptosis in the absence of ligand. The protein functions as a tumor suppressor, and is frequently mutated or downregulated in colorectal cancer and esophageal carcinoma. [provided by RefSeq, Oct 2009]","start":52340172,"end":53535903,"strand":1,"description":"DCC netrin 1 receptor [Source:HGNC Symbol;Acc:HGNC:2701]"}, {"versioned_ensembl_gene_id":"ENSG00000186409.14","gene_symbol":"CCDC30","gene_name":"coiled-coil domain containing 30 [Source:HGNC Symbol;Acc:HGNC:26103]","synonyms":"PFD6L,LOC728621,FLJ20972","biotype":"protein_coding","ncbi_id":"728621","summary":null,"start":42463330,"end":42654664,"strand":1,"description":"coiled-coil domain containing 30 [Source:HGNC Symbol;Acc:HGNC:26103]"}, {"versioned_ensembl_gene_id":"ENSG00000137959.15","gene_symbol":"IFI44L","gene_name":"interferon induced protein 44 like [Source:HGNC Symbol;Acc:HGNC:17817]","synonyms":"GS3686,C1orf29","biotype":"protein_coding","ncbi_id":"10964","summary":null,"start":78619922,"end":78646145,"strand":1,"description":"interferon induced protein 44 like [Source:HGNC Symbol;Acc:HGNC:17817]"}, {"versioned_ensembl_gene_id":"ENSG00000186767.6","gene_symbol":"SPIN4","gene_name":"spindlin family member 4 [Source:HGNC Symbol;Acc:HGNC:27040]","synonyms":"TDRD28,FLJ44984","biotype":"protein_coding","ncbi_id":"139886","summary":null,"start":63347228,"end":63351344,"strand":-1,"description":"spindlin family member 4 [Source:HGNC Symbol;Acc:HGNC:27040]"}, {"versioned_ensembl_gene_id":"ENSG00000134013.15","gene_symbol":"LOXL2","gene_name":"lysyl oxidase like 2 [Source:HGNC Symbol;Acc:HGNC:6666]","synonyms":"WS9-14,LOR","biotype":"protein_coding","ncbi_id":"4017","summary":"This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. [provided by RefSeq, Jul 2008]","start":23297189,"end":23425328,"strand":-1,"description":"lysyl oxidase like 2 [Source:HGNC Symbol;Acc:HGNC:6666]"}, {"versioned_ensembl_gene_id":"ENSG00000115274.14","gene_symbol":"INO80B","gene_name":"INO80 complex subunit B [Source:HGNC Symbol;Acc:HGNC:13324]","synonyms":"ZNHIT4,PAPA-1,PAP-1BP,IES2,HMGIYL4,HMGA1L4,hIes2","biotype":"protein_coding","ncbi_id":"83444","summary":"This gene encodes a subunit of an ATP-dependent chromatin remodeling complex, INO80, which plays a role in DNA and nucleosome-activated ATPase activity and ATP-dependent nucleosome sliding. Readthrough transcription of this gene into the neighboring downstream gene, which encodes WW domain-binding protein 1, generates a non-coding transcript. [provided by RefSeq, Feb 2011]","start":74455023,"end":74457960,"strand":1,"description":"INO80 complex subunit B [Source:HGNC Symbol;Acc:HGNC:13324]"}, {"versioned_ensembl_gene_id":"ENSG00000163793.12","gene_symbol":"DNAJC5G","gene_name":"DnaJ heat shock protein family (Hsp40) member C5 gamma [Source:HGNC Symbol;Acc:HGNC:24844]","synonyms":"FLJ40417,CSP-gamma","biotype":"protein_coding","ncbi_id":"285126","summary":null,"start":27275421,"end":27281499,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C5 gamma [Source:HGNC Symbol;Acc:HGNC:24844]"}, {"versioned_ensembl_gene_id":"ENSG00000235437.7","gene_symbol":"LINC01278","gene_name":"long intergenic non-protein coding RNA 1278 [Source:HGNC Symbol;Acc:HGNC:28090]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"92249","summary":null,"start":63343227,"end":63561071,"strand":-1,"description":"long intergenic non-protein coding RNA 1278 [Source:HGNC Symbol;Acc:HGNC:28090]"}, {"versioned_ensembl_gene_id":"ENSG00000280368.1","gene_symbol":"AC034229.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10171030,"end":10171214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260371.1","gene_symbol":"AC026464.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69335091,"end":69356306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271998.1","gene_symbol":"AC034229.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10195187,"end":10197622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260914.3","gene_symbol":"AC026464.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69299682,"end":69322700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233661.1","gene_symbol":"SPIN4-AS1","gene_name":"SPIN4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41177]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874033","summary":null,"start":63349646,"end":63352178,"strand":1,"description":"SPIN4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41177]"}, {"versioned_ensembl_gene_id":"ENSG00000260515.1","gene_symbol":"AC034229.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10195121,"end":10197628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157315.4","gene_symbol":"TMED6","gene_name":"transmembrane p24 trafficking protein 6 [Source:HGNC Symbol;Acc:HGNC:28331]","synonyms":"p24gamma5,p24g5,MGC23911","biotype":"protein_coding","ncbi_id":"146456","summary":null,"start":69343248,"end":69351809,"strand":-1,"description":"transmembrane p24 trafficking protein 6 [Source:HGNC Symbol;Acc:HGNC:28331]"}, {"versioned_ensembl_gene_id":"ENSG00000271554.1","gene_symbol":"AL138787.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35992109,"end":36013630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281965.1","gene_symbol":"AC243791.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15172578,"end":15187178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126070.19","gene_symbol":"AGO3","gene_name":"argonaute 3, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:18421]","synonyms":"EIF2C3,hAGO3,FLJ12765","biotype":"protein_coding","ncbi_id":"192669","summary":"This gene encodes a member of the Argonaute family of proteins which play a role in RNA interference. The encoded protein is highly basic, contains a PAZ domain and a PIWI domain, and may play a role in short-interfering-RNA-mediated gene silencing. This gene is located on chromosome 1 in a tandem cluster of closely related family members including argonaute 4 and eukaryotic translation initiation factor 2C, 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":35930718,"end":36072500,"strand":1,"description":"argonaute 3, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:18421]"}, {"versioned_ensembl_gene_id":"ENSG00000254531.1","gene_symbol":"FLJ20021","gene_name":"uncharacterized LOC90024 [Source:NCBI gene;Acc:90024]","synonyms":null,"biotype":"lincRNA","ncbi_id":"90024","summary":null,"start":101347780,"end":101348883,"strand":1,"description":"uncharacterized LOC90024 [Source:NCBI gene;Acc:90024]"}, {"versioned_ensembl_gene_id":"ENSG00000213380.14","gene_symbol":"COG8","gene_name":"component of oligomeric golgi complex 8 [Source:HGNC Symbol;Acc:HGNC:18623]","synonyms":"DOR1,FLJ22315,DOR1,FLJ22315","biotype":"protein_coding","ncbi_id":"84342","summary":"This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]","start":69320140,"end":69339583,"strand":-1,"description":"component of oligomeric golgi complex 8 [Source:HGNC Symbol;Acc:HGNC:18623]"}, {"versioned_ensembl_gene_id":"ENSG00000248377.1","gene_symbol":"HMGN1P9","gene_name":"high mobility group nucleosome binding domain 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:39352]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874410","summary":null,"start":134385197,"end":134385494,"strand":1,"description":"high mobility group nucleosome binding domain 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:39352]"}, {"versioned_ensembl_gene_id":"ENSG00000214288.4","gene_symbol":"HMGB3P13","gene_name":"high mobility group box 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39305]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289158","summary":null,"start":134437605,"end":134438211,"strand":1,"description":"high mobility group box 3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:39305]"}, {"versioned_ensembl_gene_id":"ENSG00000255237.1","gene_symbol":"AC138230.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":462930,"end":463899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281994.1","gene_symbol":"NPIPA1","gene_name":"nuclear pore complex interacting protein family member A1 [Source:HGNC Symbol;Acc:HGNC:7909]","synonyms":"NPIP,morpheus","biotype":"protein_coding","ncbi_id":"9284","summary":null,"start":15144756,"end":15171447,"strand":-1,"description":"nuclear pore complex interacting protein family member A1 [Source:HGNC Symbol;Acc:HGNC:7909]"}, {"versioned_ensembl_gene_id":"ENSG00000258429.1","gene_symbol":"PDF","gene_name":"peptide deformylase (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:30012]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64146","summary":"Protein synthesis proceeds after formylation of methionine by methionyl-tRNA formyl transferase (FMT) and transfer of the charged initiator f-met tRNA to the ribosome. In eubacteria and eukaryotic organelles the product of this gene, peptide deformylase (PDF), removes the formyl group from the initiating methionine of nascent peptides. In eubacteria, deformylation of nascent peptides is required for subsequent cleavage of initiating methionines by methionine aminopeptidase. The discovery that a natural inhibitor of PDF, actinonin, acts as an antimicrobial agent in some bacteria has spurred intensive research into the design of bacterial-specific PDF inhibitors. In human cells, only mitochondrial proteins have N-formylation of initiating methionines. Protein inhibitors of PDF or siRNAs of PDF block the growth of cancer cell lines but have no effect on normal cell growth. In humans, PDF function may therefore be restricted to rapidly growing cells. [provided by RefSeq, Nov 2008]","start":69328621,"end":69330595,"strand":-1,"description":"peptide deformylase (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:30012]"}, {"versioned_ensembl_gene_id":"ENSG00000226427.1","gene_symbol":"HMGN2P7","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33575]","synonyms":"HMGN2L7","biotype":"processed_pseudogene","ncbi_id":"644498","summary":null,"start":15375373,"end":15375645,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:33575]"}, {"versioned_ensembl_gene_id":"ENSG00000108590.10","gene_symbol":"MED31","gene_name":"mediator complex subunit 31 [Source:HGNC Symbol;Acc:HGNC:24260]","synonyms":"Soh1,CGI-125","biotype":"protein_coding","ncbi_id":"51003","summary":null,"start":6643315,"end":6651634,"strand":-1,"description":"mediator complex subunit 31 [Source:HGNC Symbol;Acc:HGNC:24260]"}, {"versioned_ensembl_gene_id":"ENSG00000253837.1","gene_symbol":"AC090197.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23336171,"end":23366125,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197217.12","gene_symbol":"ENTPD4","gene_name":"ectonucleoside triphosphate diphosphohydrolase 4 [Source:HGNC Symbol;Acc:HGNC:14573]","synonyms":"UDPase,NTPDase-4,LYSAL1,LAP70,LALP70,KIAA0392","biotype":"protein_coding","ncbi_id":"9583","summary":"This gene encodes a member of the apyrase protein family. Apyrases are enzymes that catalyze the hydrolysis of nucleotide diphosphates and triphosphates in a calcium or magnesium-dependent manner. The encoded protein is an endo-apyrase and may play a role in salvaging nucleotides from lysosomes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and these isoforms may differ in divalent cation dependence and substrate specificity. [provided by RefSeq, Sep 2011]","start":23385783,"end":23457695,"strand":-1,"description":"ectonucleoside triphosphate diphosphohydrolase 4 [Source:HGNC Symbol;Acc:HGNC:14573]"}, {"versioned_ensembl_gene_id":"ENSG00000259900.5","gene_symbol":"AC026464.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":69335276,"end":69351730,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269505.2","gene_symbol":"ZNF92P2","gene_name":"zinc finger protein 92 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419705","summary":null,"start":22128627,"end":22130318,"strand":-1,"description":"zinc finger protein 92 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39554]"}, {"versioned_ensembl_gene_id":"ENSG00000197358.9","gene_symbol":"BNIP3P1","gene_name":"BCL2 interacting protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19922]","synonyms":"BNIP3P","biotype":"transcribed_processed_pseudogene","ncbi_id":"319138","summary":null,"start":28264390,"end":28265974,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19922]"}, {"versioned_ensembl_gene_id":"ENSG00000130313.6","gene_symbol":"PGLS","gene_name":"6-phosphogluconolactonase [Source:HGNC Symbol;Acc:HGNC:8903]","synonyms":"6PGL","biotype":"protein_coding","ncbi_id":"25796","summary":null,"start":17511629,"end":17521288,"strand":1,"description":"6-phosphogluconolactonase [Source:HGNC Symbol;Acc:HGNC:8903]"}, {"versioned_ensembl_gene_id":"ENSG00000118271.9","gene_symbol":"TTR","gene_name":"transthyretin [Source:HGNC Symbol;Acc:HGNC:12405]","synonyms":"PALB,HsT2651,CTS1,CTS","biotype":"protein_coding","ncbi_id":"7276","summary":"This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome. [provided by RefSeq, Aug 2017]","start":31591726,"end":31599021,"strand":1,"description":"transthyretin [Source:HGNC Symbol;Acc:HGNC:12405]"}, {"versioned_ensembl_gene_id":"ENSG00000079739.15","gene_symbol":"PGM1","gene_name":"phosphoglucomutase 1 [Source:HGNC Symbol;Acc:HGNC:8905]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5236","summary":"The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]","start":63593276,"end":63660245,"strand":1,"description":"phosphoglucomutase 1 [Source:HGNC Symbol;Acc:HGNC:8905]"}, {"versioned_ensembl_gene_id":"ENSG00000103044.10","gene_symbol":"HAS3","gene_name":"hyaluronan synthase 3 [Source:HGNC Symbol;Acc:HGNC:4820]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3038","summary":"The protein encoded by this gene is involved in the synthesis of the unbranched glycosaminoglycan hyaluronan, or hyaluronic acid, which is a major constituent of the extracellular matrix. This gene is a member of the NODC/HAS gene family. Compared to the proteins encoded by other members of this gene family, this protein appears to be more of a regulator of hyaluronan synthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]","start":69105564,"end":69118719,"strand":1,"description":"hyaluronan synthase 3 [Source:HGNC Symbol;Acc:HGNC:4820]"}, {"versioned_ensembl_gene_id":"ENSG00000276709.4","gene_symbol":"PDXDC1","gene_name":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]","synonyms":"KIAA0251,KIAA0251","biotype":"protein_coding","ncbi_id":"23042","summary":null,"start":15241230,"end":15297417,"strand":1,"description":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]"}, {"versioned_ensembl_gene_id":"ENSG00000233024.7","gene_symbol":"AC126755.2","gene_name":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18358086,"end":18379331,"strand":-1,"description":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]"}, {"versioned_ensembl_gene_id":"ENSG00000239779.6","gene_symbol":"WBP1","gene_name":"WW domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12737]","synonyms":"WBP-1","biotype":"protein_coding","ncbi_id":"23559","summary":"The globular WW domain, named for the conserved tryptophan residues in the protein motif present in various structural and regulatory proteins, is known to play a role in the mediation of protein-protein interactions. This gene encodes a ligand of the WW domain of the Yes kinase-associated protein. Readthrough transcription of the neighboring upstream gene, which encodes INO80 complex subunit B, into this gene generates a non-coding transcript. [provided by RefSeq, Feb 2011]","start":74458329,"end":74460891,"strand":1,"description":"WW domain binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12737]"}, {"versioned_ensembl_gene_id":"ENSG00000198920.9","gene_symbol":"KIAA0753","gene_name":"KIAA0753 [Source:HGNC Symbol;Acc:HGNC:29110]","synonyms":"OFIP,MNR","biotype":"protein_coding","ncbi_id":"9851","summary":"This gene encodes a subunit of a protein complex that regulates ciliogenesis and cilia maintenance. The encoded protein has also been shown to regulate centriolar duplication. Mutations in this gene cause an orofaciodigital syndrome and a form of Joubert syndrome in human patients. [provided by RefSeq, May 2017]","start":6578148,"end":6640927,"strand":-1,"description":"KIAA0753 [Source:HGNC Symbol;Acc:HGNC:29110]"}, {"versioned_ensembl_gene_id":"ENSG00000214081.8","gene_symbol":"CYP4F30P","gene_name":"cytochrome P450 family 4 subfamily F member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:25270]","synonyms":"DKFZp434F1719,C2orf14,4F-se9[6:7:8]","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132708","summary":null,"start":130680050,"end":130685863,"strand":1,"description":"cytochrome P450 family 4 subfamily F member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:25270]"}, {"versioned_ensembl_gene_id":"ENSG00000228108.1","gene_symbol":"AC092839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54516048,"end":54540697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250514.1","gene_symbol":"LINC02125","gene_name":"long intergenic non-protein coding RNA 2125 [Source:HGNC Symbol;Acc:HGNC:52982]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928203","summary":null,"start":76634998,"end":76658478,"strand":1,"description":"long intergenic non-protein coding RNA 2125 [Source:HGNC Symbol;Acc:HGNC:52982]"}, {"versioned_ensembl_gene_id":"ENSG00000238018.2","gene_symbol":"AC093110.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54661011,"end":54680045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260797.1","gene_symbol":"AC106734.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76878274,"end":76878936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223349.1","gene_symbol":"KLF2P3","gene_name":"Kruppel like factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49282]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481672","summary":null,"start":130692243,"end":130693770,"strand":-1,"description":"Kruppel like factor 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49282]"}, {"versioned_ensembl_gene_id":"ENSG00000237887.1","gene_symbol":"RPL23AP32","gene_name":"ribosomal protein L23a pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:25345]","synonyms":"DKFZp547I014","biotype":"processed_pseudogene","ncbi_id":"56969","summary":"This locus represents a transcribed pseudogene of ribosomal protein L23a. [provided by RefSeq, Aug 2011]","start":54529343,"end":54529801,"strand":1,"description":"ribosomal protein L23a pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:25345]"}, {"versioned_ensembl_gene_id":"ENSG00000273659.1","gene_symbol":"AC108125.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76582556,"end":76583098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282944.1","gene_symbol":"AC140481.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":130681228,"end":130691691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259995.1","gene_symbol":"AC106729.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":76736342,"end":76928169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125630.15","gene_symbol":"POLR1B","gene_name":"RNA polymerase I subunit B [Source:HGNC Symbol;Acc:HGNC:20454]","synonyms":"Rpo1-2,RPA2,FLJ21921,FLJ10816","biotype":"protein_coding","ncbi_id":"84172","summary":"Eukaryotic RNA polymerase I (pol I) is responsible for the transcription of ribosomal RNA (rRNA) genes and production of rRNA, the primary component of ribosomes. Pol I is a multisubunit enzyme composed of 6 to 14 polypeptides, depending on the species. Most of the mass of the pol I complex derives from the 2 largest subunits, Rpa1 and Rpa2 in yeast. POLR1B is homologous to Rpa2 (Seither and Grummt, 1996 [PubMed 8921381]).[supplied by OMIM, Mar 2008]","start":112541915,"end":112577150,"strand":1,"description":"RNA polymerase I subunit B [Source:HGNC Symbol;Acc:HGNC:20454]"}, {"versioned_ensembl_gene_id":"ENSG00000249691.1","gene_symbol":"AC026117.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":134510531,"end":134511413,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261833.2","gene_symbol":"AC104151.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":76553417,"end":76819624,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240253.5","gene_symbol":"FAR2P3","gene_name":"fatty acyl-CoA reductase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49285]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288897","summary":null,"start":130690133,"end":130718831,"strand":1,"description":"fatty acyl-CoA reductase 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49285]"}, {"versioned_ensembl_gene_id":"ENSG00000230116.1","gene_symbol":"AL445669.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42491739,"end":42492493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235282.3","gene_symbol":"DYNLL1P3","gene_name":"dynein light chain LC8-type 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49654]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391012","summary":null,"start":18513118,"end":18513383,"strand":1,"description":"dynein light chain LC8-type 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49654]"}, {"versioned_ensembl_gene_id":"ENSG00000115306.15","gene_symbol":"SPTBN1","gene_name":"spectrin beta, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11275]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6711","summary":"Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is composed of two antiparallel dimers of alpha- and beta- subunits. This gene is one member of a family of beta-spectrin genes. The encoded protein contains an N-terminal actin-binding domain, and 17 spectrin repeats which are involved in dimer formation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54456285,"end":54671445,"strand":1,"description":"spectrin beta, non-erythrocytic 1 [Source:HGNC Symbol;Acc:HGNC:11275]"}, {"versioned_ensembl_gene_id":"ENSG00000279964.1","gene_symbol":"AC009949.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":230410700,"end":230412529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182923.16","gene_symbol":"CEP63","gene_name":"centrosomal protein 63 [Source:HGNC Symbol;Acc:HGNC:25815]","synonyms":"FLJ13386","biotype":"protein_coding","ncbi_id":"80254","summary":"This gene encodes a protein with six coiled-coil domains. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. Several alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":134485743,"end":134575017,"strand":1,"description":"centrosomal protein 63 [Source:HGNC Symbol;Acc:HGNC:25815]"}, {"versioned_ensembl_gene_id":"ENSG00000111834.12","gene_symbol":"RSPH4A","gene_name":"radial spoke head 4 homolog A [Source:HGNC Symbol;Acc:HGNC:21558]","synonyms":"RSPH6B,RSHL3,FLJ37974,dJ412I7.1,CILD11","biotype":"protein_coding","ncbi_id":"345895","summary":"This gene encodes a protein that appears to be a component the radial spoke head, as determined by homology to similar proteins in the biflagellate alga Chlamydomonas reinhardtii and other ciliates. Radial spokes, which are regularly spaced along cilia, sperm, and flagella axonemes, consist of a thin 'stalk' and a bulbous 'head' that form a signal transduction scaffold between the central pair of microtubules and dynein. Mutations in this gene cause primary ciliary dyskinesia 1, a disease arising from dysmotility of motile cilia and sperm. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":116616479,"end":116632985,"strand":1,"description":"radial spoke head 4 homolog A [Source:HGNC Symbol;Acc:HGNC:21558]"}, {"versioned_ensembl_gene_id":"ENSG00000179111.8","gene_symbol":"HES7","gene_name":"hes family bHLH transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:15977]","synonyms":"bHLHb37","biotype":"protein_coding","ncbi_id":"84667","summary":"This gene encodes a member of the hairy and enhancer of split family of bHLH transcription factors. The mouse ortholog of this gene is regulated by Notch signaling. The protein functions as a transcriptional repressor, and is implicated in correct patterning of the axial skeleton. A mutation in this gene has been shown to result in spondylocostal dysostosis. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":8120590,"end":8124092,"strand":-1,"description":"hes family bHLH transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:15977]"}, {"versioned_ensembl_gene_id":"ENSG00000132612.15","gene_symbol":"VPS4A","gene_name":"vacuolar protein sorting 4 homolog A [Source:HGNC Symbol;Acc:HGNC:13488]","synonyms":"VPS4,SKD2,SKD1A,SKD1,FLJ22197,VPS4-1","biotype":"protein_coding","ncbi_id":"27183","summary":"The protein encoded by this gene is a member of the AAA protein family (ATPases associated with diverse cellular activities), and is the homolog of the yeast Vps4 protein. In humans, two paralogs of the yeast protein have been identified. The former share a high degree of aa sequence similarity with each other, and also with yeast Vps4 and mouse Skd1 proteins. The mouse Skd1 (suppressor of K+ transport defect 1) has been shown to be really an yeast Vps4 ortholog. Functional studies indicate that both human paralogs associate with the endosomal compartments, and are involved in intracellular protein trafficking, similar to Vps4 protein in yeast. The gene encoding this paralog has been mapped to chromosome 16; the gene for the other resides on chromosome 18. [provided by RefSeq, Jul 2008]","start":69311356,"end":69326939,"strand":1,"description":"vacuolar protein sorting 4 homolog A [Source:HGNC Symbol;Acc:HGNC:13488]"}, {"versioned_ensembl_gene_id":"ENSG00000227803.2","gene_symbol":"AL158198.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20212087,"end":20317739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172197.10","gene_symbol":"MBOAT1","gene_name":"membrane bound O-acyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21579]","synonyms":"OACT1,MGC44669,LPEAT1,dJ434O11.1","biotype":"protein_coding","ncbi_id":"154141","summary":"This gene belongs to the membrane-bound O-acetyltransferase superfamily. The encoded transmembrane protein is an enzyme that transfers organic compounds, preferably from oleoyl-CoA, to hydroxyl groups of protein targets in membranes. A translocation disrupting this gene may be associated with brachydactyly syndactyly syndrome. Alternately spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]","start":20102145,"end":20212399,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21579]"}, {"versioned_ensembl_gene_id":"ENSG00000254681.6","gene_symbol":"PKD1P5","gene_name":"polycystin 1, transient receptor potential channel interacting pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30069]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"348156","summary":null,"start":18374521,"end":18401940,"strand":-1,"description":"polycystin 1, transient receptor potential channel interacting pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:30069]"}, {"versioned_ensembl_gene_id":"ENSG00000100263.13","gene_symbol":"RHBDD3","gene_name":"rhomboid domain containing 3 [Source:HGNC Symbol;Acc:HGNC:1308]","synonyms":"PTAG,C22orf3","biotype":"protein_coding","ncbi_id":"25807","summary":null,"start":29259852,"end":29268209,"strand":-1,"description":"rhomboid domain containing 3 [Source:HGNC Symbol;Acc:HGNC:1308]"}, {"versioned_ensembl_gene_id":"ENSG00000251192.7","gene_symbol":"ZNF674","gene_name":"zinc finger protein 674 [Source:HGNC Symbol;Acc:HGNC:17625]","synonyms":"MRX92,ZNF673B","biotype":"protein_coding","ncbi_id":"641339","summary":"This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disabilities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]","start":46497727,"end":46545457,"strand":-1,"description":"zinc finger protein 674 [Source:HGNC Symbol;Acc:HGNC:17625]"}, {"versioned_ensembl_gene_id":"ENSG00000066185.12","gene_symbol":"ZMYND12","gene_name":"zinc finger MYND-type containing 12 [Source:HGNC Symbol;Acc:HGNC:21192]","synonyms":"DKFZp434N2435","biotype":"protein_coding","ncbi_id":"84217","summary":null,"start":42430329,"end":42456267,"strand":-1,"description":"zinc finger MYND-type containing 12 [Source:HGNC Symbol;Acc:HGNC:21192]"}, {"versioned_ensembl_gene_id":"ENSG00000124571.17","gene_symbol":"XPO5","gene_name":"exportin 5 [Source:HGNC Symbol;Acc:HGNC:17675]","synonyms":"KIAA1291","biotype":"protein_coding","ncbi_id":"57510","summary":"This gene encodes a member of the karyopherin family that is required for the transport of small RNAs and double-stranded RNA-binding proteins from the nucleus to the cytoplasm. The encoded protein translocates cargo through the nuclear pore complex in a RanGTP-dependent process. [provided by RefSeq, Aug 2011]","start":43522330,"end":43576075,"strand":-1,"description":"exportin 5 [Source:HGNC Symbol;Acc:HGNC:17675]"}, {"versioned_ensembl_gene_id":"ENSG00000164683.16","gene_symbol":"HEY1","gene_name":"hes related family bHLH transcription factor with YRPW motif 1 [Source:HGNC Symbol;Acc:HGNC:4880]","synonyms":"HRT-1,HESR1,HESR-1,HERP2,CHF2,CHF-2,bHLHb31","biotype":"protein_coding","ncbi_id":"23462","summary":"This gene encodes a nuclear protein belonging to the hairy and enhancer of split-related (HESR) family of basic helix-loop-helix (bHLH)-type transcriptional repressors. Expression of this gene is induced by the Notch and c-Jun signal transduction pathways. Two similar and redundant genes in mouse are required for embryonic cardiovascular development, and are also implicated in neurogenesis and somitogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":79764010,"end":79767863,"strand":-1,"description":"hes related family bHLH transcription factor with YRPW motif 1 [Source:HGNC Symbol;Acc:HGNC:4880]"}, {"versioned_ensembl_gene_id":"ENSG00000268116.1","gene_symbol":"AC073539.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22130325,"end":22130489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269161.1","gene_symbol":"AC010618.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17518330,"end":17520565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234804.1","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"hs6M1-4,OR6-5,dJ80I19.2,OR2J1P","biotype":"unprocessed_pseudogene","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29097608,"end":29098546,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000232178.1","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29108558,"end":29109493,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000232272.1","gene_symbol":"AL662852.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29120878,"end":29125574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275914.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"nkat6,CD158k,cl-43,CD158B1","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754693,"end":54769187,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000168807.16","gene_symbol":"SNTB2","gene_name":"syntrophin beta 2 [Source:HGNC Symbol;Acc:HGNC:11169]","synonyms":"D16S2531E,SNTL,SNT3,SNT2B2,EST25263","biotype":"protein_coding","ncbi_id":"6645","summary":"Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]","start":69187129,"end":69309052,"strand":1,"description":"syntrophin beta 2 [Source:HGNC Symbol;Acc:HGNC:11169]"}, {"versioned_ensembl_gene_id":"ENSG00000142748.12","gene_symbol":"FCN3","gene_name":"ficolin 3 [Source:HGNC Symbol;Acc:HGNC:3625]","synonyms":"HAKA1,FCNH","biotype":"protein_coding","ncbi_id":"8547","summary":"Ficolins are a group of proteins which consist of a collagen-like domain and a fibrinogen-like domain. In human serum, there are two types of ficolins, both of which have lectin activity. The protein encoded by this gene is a thermolabile beta-2-macroglycoprotein found in all human serum and is a member of the ficolin/opsonin p35 lectin family. The protein, which was initially identified based on its reactivity with sera from patients with systemic lupus erythematosus, has been shown to have a calcium-independent lectin activity. The protein can activate the complement pathway in association with MASPs and sMAP, thereby aiding in host defense through the activation of the lectin pathway. Alternative splicing occurs at this locus and two variants, each encoding a distinct isoform, have been identified. [provided by RefSeq, Jul 2008]","start":27369112,"end":27374824,"strand":-1,"description":"ficolin 3 [Source:HGNC Symbol;Acc:HGNC:3625]"}, {"versioned_ensembl_gene_id":"ENSG00000274438.1","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"183ActI,CD158J,cl-49,nkat5","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738507,"end":54752802,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000237243.1","gene_symbol":"AC022173.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137953348,"end":137957966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269439.5","gene_symbol":"AC010618.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17488990,"end":17511889,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182158.14","gene_symbol":"CREB3L2","gene_name":"cAMP responsive element binding protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:23720]","synonyms":"BBF2H7,TCAG_1951439","biotype":"protein_coding","ncbi_id":"64764","summary":"This gene encodes a member of the oasis bZIP transcription factor family. Members of this family can dimerize but form homodimers only. The encoded protein is a transcriptional activator. Translocations between this gene on chromosome 7 and the gene fused in sarcoma on chromosome 16 can be found in some tumors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":137874979,"end":138002067,"strand":-1,"description":"cAMP responsive element binding protein 3 like 2 [Source:HGNC Symbol;Acc:HGNC:23720]"}, {"versioned_ensembl_gene_id":"ENSG00000275513.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724485,"end":54736502,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000236876.3","gene_symbol":"TMSB4XP1","gene_name":"thymosin beta 4, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11883]","synonyms":"TMSL1","biotype":"processed_pseudogene","ncbi_id":"7115","summary":null,"start":42500205,"end":42500339,"strand":-1,"description":"thymosin beta 4, X-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11883]"}, {"versioned_ensembl_gene_id":"ENSG00000249786.7","gene_symbol":"EAF1-AS1","gene_name":"EAF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42328]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873956","summary":null,"start":15436171,"end":15455940,"strand":-1,"description":"EAF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42328]"}, {"versioned_ensembl_gene_id":"ENSG00000268140.1","gene_symbol":"PCGF7P","gene_name":"polycomb group ring finger 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:30341]","synonyms":"RNF134P1","biotype":"processed_pseudogene","ncbi_id":"253272","summary":null,"start":22137931,"end":22138981,"strand":1,"description":"polycomb group ring finger 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:30341]"}, {"versioned_ensembl_gene_id":"ENSG00000269575.1","gene_symbol":"MTDHP5","gene_name":"metadherin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418836","summary":null,"start":22140532,"end":22141117,"strand":1,"description":"metadherin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52361]"}, {"versioned_ensembl_gene_id":"ENSG00000236180.2","gene_symbol":"AL445669.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42570970,"end":42571390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196747.4","gene_symbol":"HIST1H2AI","gene_name":"histone cluster 1 H2A family member i [Source:HGNC Symbol;Acc:HGNC:4725]","synonyms":"H2AFC,H2A/c","biotype":"protein_coding","ncbi_id":"8329","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27808199,"end":27808701,"strand":1,"description":"histone cluster 1 H2A family member i [Source:HGNC Symbol;Acc:HGNC:4725]"}, {"versioned_ensembl_gene_id":"ENSG00000269345.1","gene_symbol":"VN1R85P","gene_name":"vomeronasal 1 receptor 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:37405]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312830","summary":null,"start":22174766,"end":22175191,"strand":-1,"description":"vomeronasal 1 receptor 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:37405]"}, {"versioned_ensembl_gene_id":"ENSG00000127125.8","gene_symbol":"PPCS","gene_name":"phosphopantothenoylcysteine synthetase [Source:HGNC Symbol;Acc:HGNC:25686]","synonyms":"FLJ11838","biotype":"protein_coding","ncbi_id":"79717","summary":"Biosynthesis of coenzyme A (CoA) from pantothenic acid (vitamin B5) is an essential universal pathway in prokaryotes and eukaryotes. PPCS (EC 6.3.2.5), one of the last enzymes in this pathway, converts phosphopantothenate to phosphopantothenoylcysteine (Daugherty et al., 2002 [PubMed 11923312]).[supplied by OMIM, Mar 2008]","start":42456117,"end":42473385,"strand":1,"description":"phosphopantothenoylcysteine synthetase [Source:HGNC Symbol;Acc:HGNC:25686]"}, {"versioned_ensembl_gene_id":"ENSG00000257869.1","gene_symbol":"AL139023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28318141,"end":28418612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182944.17","gene_symbol":"EWSR1","gene_name":"EWS RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3508]","synonyms":"EWS","biotype":"protein_coding","ncbi_id":"2130","summary":"This gene encodes a multifunctional protein that is involved in various cellular processes, including gene expression, cell signaling, and RNA processing and transport. The protein includes an N-terminal transcriptional activation domain and a C-terminal RNA-binding domain. Chromosomal translocations between this gene and various genes encoding transcription factors result in the production of chimeric proteins that are involved in tumorigenesis. These chimeric proteins usually consist of the N-terminal transcriptional activation domain of this protein fused to the C-terminal DNA-binding domain of the transcription factor protein. Mutations in this gene, specifically a t(11;22)(q24;q12) translocation, are known to cause Ewing sarcoma as well as neuroectodermal and various other tumors. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and 14. [provided by RefSeq, Jul 2009]","start":29268009,"end":29300525,"strand":1,"description":"EWS RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3508]"}, {"versioned_ensembl_gene_id":"ENSG00000196109.6","gene_symbol":"ZNF676","gene_name":"zinc finger protein 676 [Source:HGNC Symbol;Acc:HGNC:20429]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163223","summary":null,"start":22179091,"end":22196951,"strand":-1,"description":"zinc finger protein 676 [Source:HGNC Symbol;Acc:HGNC:20429]"}, {"versioned_ensembl_gene_id":"ENSG00000273769.5","gene_symbol":"LCA10","gene_name":"lung carcinoma-associated 10 [Source:NCBI gene;Acc:100996465]","synonyms":"LCAP","biotype":"processed_transcript","ncbi_id":"100996465","summary":null,"start":153880672,"end":153888990,"strand":1,"description":"lung carcinoma-associated 10 [Source:NCBI gene;Acc:100996465]"}, {"versioned_ensembl_gene_id":"ENSG00000278828.1","gene_symbol":"HIST1H3H","gene_name":"histone cluster 1 H3 family member h [Source:HGNC Symbol;Acc:HGNC:4775]","synonyms":"H3FK,H3F1K,H3/k","biotype":"protein_coding","ncbi_id":"8357","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27810064,"end":27811300,"strand":1,"description":"histone cluster 1 H3 family member h [Source:HGNC Symbol;Acc:HGNC:4775]"}, {"versioned_ensembl_gene_id":"ENSG00000206562.11","gene_symbol":"METTL6","gene_name":"methyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:28343]","synonyms":"MGC24132","biotype":"protein_coding","ncbi_id":"131965","summary":null,"start":15381275,"end":15440566,"strand":-1,"description":"methyltransferase like 6 [Source:HGNC Symbol;Acc:HGNC:28343]"}, {"versioned_ensembl_gene_id":"ENSG00000240179.1","gene_symbol":"AL133162.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28489910,"end":28490362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282936.1","gene_symbol":"AC004706.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6636780,"end":6640316,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268079.1","gene_symbol":"BNIP3P30","gene_name":"BCL2 interacting protein 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49710]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481694","summary":null,"start":22203128,"end":22204003,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49710]"}, {"versioned_ensembl_gene_id":"ENSG00000213809.8","gene_symbol":"KLRK1","gene_name":"killer cell lectin like receptor K1 [Source:HGNC Symbol;Acc:HGNC:18788]","synonyms":"NKG2D,NKG2-D,KLR,D12S2489E,CD314","biotype":"protein_coding","ncbi_id":"22914","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed in NK cells. This gene encodes a member of the NKG2 family. The encoded transmembrane protein is characterized by a type II membrane orientation (has an extracellular C terminus) and the presence of a C-type lectin domain. It binds to a diverse family of ligands that include MHC class I chain-related A and B proteins and UL-16 binding proteins, where ligand-receptor interactions can result in the activation of NK and T cells. The surface expression of these ligands is important for the recognition of stressed cells by the immune system, and thus this protein and its ligands are therapeutic targets for the treatment of immune diseases and cancers. Read-through transcription exists between this gene and the upstream KLRC4 (killer cell lectin-like receptor subfamily C, member 4) family member in the same cluster. [provided by RefSeq, Dec 2010]","start":10372353,"end":10391874,"strand":-1,"description":"killer cell lectin like receptor K1 [Source:HGNC Symbol;Acc:HGNC:18788]"}, {"versioned_ensembl_gene_id":"ENSG00000126895.13","gene_symbol":"AVPR2","gene_name":"arginine vasopressin receptor 2 [Source:HGNC Symbol;Acc:HGNC:897]","synonyms":"V2R,DIR3,DIR","biotype":"protein_coding","ncbi_id":"554","summary":"This gene encodes the vasopressin receptor, type 2, also known as the V2 receptor, which belongs to the seven-transmembrane-domain G protein-coupled receptor (GPCR) superfamily, and couples to Gs thus stimulating adenylate cyclase. The subfamily that includes the V2 receptor, the V1a and V1b vasopressin receptors, the oxytocin receptor, and isotocin and mesotocin receptors in non-mammals, is well conserved, though several members signal via other G proteins. All bind similar cyclic nonapeptide hormones. The V2 receptor is expressed in the kidney tubule, predominantly in the distal convoluted tubule and collecting ducts, where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism. When the function of this gene is lost, the disease Nephrogenic Diabetes Insipidus (NDI) results. The V2 receptor is also expressed outside the kidney although its tissue localization is uncertain. When these 'extrarenal receptors' are stimulated by infusion of a V2 selective agonist (dDAVP), a variety of clotting factors are released into the bloodstream. The physiologic importance of this property is not known - its absence does not appear to be detrimental in NDI patients. The gene expression has also been described in fetal lung tissue and lung cancer associated with alternative splicing. [provided by RefSeq, Jul 2008]","start":153902531,"end":153907166,"strand":1,"description":"arginine vasopressin receptor 2 [Source:HGNC Symbol;Acc:HGNC:897]"}, {"versioned_ensembl_gene_id":"ENSG00000153789.12","gene_symbol":"FAM92B","gene_name":"family with sequence similarity 92 member B [Source:HGNC Symbol;Acc:HGNC:24781]","synonyms":"FLJ44299","biotype":"protein_coding","ncbi_id":"339145","summary":null,"start":85098358,"end":85112508,"strand":-1,"description":"family with sequence similarity 92 member B [Source:HGNC Symbol;Acc:HGNC:24781]"}, {"versioned_ensembl_gene_id":"ENSG00000141076.17","gene_symbol":"UTP4","gene_name":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]","synonyms":"TEX292,NAIC,KIAA1988,FLJ14728,CIRHIN,CIRH1A","biotype":"protein_coding","ncbi_id":"84916","summary":"This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":69131291,"end":69231130,"strand":1,"description":"UTP4, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:1983]"}, {"versioned_ensembl_gene_id":"ENSG00000224338.2","gene_symbol":"MTCYBP45","gene_name":"mitochondrially encoded cytochrome b pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52313]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729120","summary":null,"start":11425257,"end":11425821,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52313]"}, {"versioned_ensembl_gene_id":"ENSG00000274049.4","gene_symbol":"INO80B-WBP1","gene_name":"INO80B-WBP1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49199]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100532735","summary":"This locus represents naturally occurring read-through transcription between the neighboring INO80B (INO80 complex subunit B) and WBP1 (WW domain-binding protein 1) genes on chromosome 2. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":74455088,"end":74460884,"strand":1,"description":"INO80B-WBP1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49199]"}, {"versioned_ensembl_gene_id":"ENSG00000132967.9","gene_symbol":"HMGB1P5","gene_name":"high mobility group box 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4997]","synonyms":"HMGB1L5,HMGB1L15,HMG1L5,HMGB1P2","biotype":"transcribed_processed_pseudogene","ncbi_id":"10354","summary":null,"start":22381819,"end":22382929,"strand":1,"description":"high mobility group box 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:4997]"}, {"versioned_ensembl_gene_id":"ENSG00000224925.2","gene_symbol":"AL662852.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29134543,"end":29135479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273387.1","gene_symbol":"AC005005.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31082156,"end":31083565,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228015.1","gene_symbol":"AC074338.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33128988,"end":33129143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278920.1","gene_symbol":"AC005005.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":31051630,"end":31068327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233822.4","gene_symbol":"HIST1H2BN","gene_name":"histone cluster 1 H2B family member n [Source:HGNC Symbol;Acc:HGNC:4749]","synonyms":"H2BFD,H2B/d","biotype":"protein_coding","ncbi_id":"8341","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27837760,"end":27865798,"strand":1,"description":"histone cluster 1 H2B family member n [Source:HGNC Symbol;Acc:HGNC:4749]"}, {"versioned_ensembl_gene_id":"ENSG00000234723.1","gene_symbol":"AC092421.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22670201,"end":22670711,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226441.2","gene_symbol":"PLCL2-AS1","gene_name":"PLCL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40449]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874003","summary":null,"start":17042742,"end":17044192,"strand":-1,"description":"PLCL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40449]"}, {"versioned_ensembl_gene_id":"ENSG00000257662.1","gene_symbol":"EIF4A1P12","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37933]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462830","summary":null,"start":28593779,"end":28593919,"strand":1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37933]"}, {"versioned_ensembl_gene_id":"ENSG00000183963.18","gene_symbol":"SMTN","gene_name":"smoothelin [Source:HGNC Symbol;Acc:HGNC:11126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6525","summary":"This gene encodes a structural protein that is found exclusively in contractile smooth muscle cells. It associates with stress fibers and constitutes part of the cytoskeleton. This gene is localized to chromosome 22q12.3, distal to the TUPLE1 locus and outside the DiGeorge syndrome deletion. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2011]","start":31064105,"end":31104757,"strand":1,"description":"smoothelin [Source:HGNC Symbol;Acc:HGNC:11126]"}, {"versioned_ensembl_gene_id":"ENSG00000163993.6","gene_symbol":"S100P","gene_name":"S100 calcium binding protein P [Source:HGNC Symbol;Acc:HGNC:10504]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6286","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 4p16. This protein, in addition to binding Ca2+, also binds Zn2+ and Mg2+. This protein may play a role in the etiology of prostate cancer. [provided by RefSeq, Jul 2008]","start":6693069,"end":6697170,"strand":1,"description":"S100 calcium binding protein P [Source:HGNC Symbol;Acc:HGNC:10504]"}, {"versioned_ensembl_gene_id":"ENSG00000154822.17","gene_symbol":"PLCL2","gene_name":"phospholipase C like 2 [Source:HGNC Symbol;Acc:HGNC:9064]","synonyms":"KIAA1092,PLCE2","biotype":"protein_coding","ncbi_id":"23228","summary":null,"start":16802651,"end":17090594,"strand":1,"description":"phospholipase C like 2 [Source:HGNC Symbol;Acc:HGNC:9064]"}, {"versioned_ensembl_gene_id":"ENSG00000258175.1","gene_symbol":"LINC02300","gene_name":"long intergenic non-protein coding RNA 2300 [Source:HGNC Symbol;Acc:HGNC:53219]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370422","summary":null,"start":28592223,"end":28613623,"strand":-1,"description":"long intergenic non-protein coding RNA 2300 [Source:HGNC Symbol;Acc:HGNC:53219]"}, {"versioned_ensembl_gene_id":"ENSG00000262993.1","gene_symbol":"KRT31","gene_name":"keratin 31 [Source:HGNC Symbol;Acc:HGNC:6448]","synonyms":"Ha-1,KRTHA1","biotype":"protein_coding","ncbi_id":"3881","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41401024,"end":41404892,"strand":-1,"description":"keratin 31 [Source:HGNC Symbol;Acc:HGNC:6448]"}, {"versioned_ensembl_gene_id":"ENSG00000278466.3","gene_symbol":"MUC2","gene_name":"mucin 2, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7512]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4583","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. The protein polymerizes into a gel of which 80% is composed of oligosaccharide side chains by weight. The protein features a central domain containing tandem repeats rich in threonine and proline that varies between 50 and 115 copies in different individuals. Downregulation of this gene has been observed in patients with Crohn disease and ulcerative colitis. [provided by RefSeq, Oct 2016]","start":1086525,"end":1116069,"strand":1,"description":"mucin 2, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7512]"}, {"versioned_ensembl_gene_id":"ENSG00000282732.1","gene_symbol":"AC073539.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22215634,"end":22215661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267872.1","gene_symbol":"AC073539.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22243254,"end":22245347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230912.1","gene_symbol":"AL021707.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38666508,"end":38668750,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268597.1","gene_symbol":"AC073539.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22259693,"end":22261335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261897.1","gene_symbol":"OR5T3","gene_name":"olfactory receptor family 5 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:15297]","synonyms":"OR5T3Q","biotype":"protein_coding","ncbi_id":"390154","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56252200,"end":56253222,"strand":1,"description":"olfactory receptor family 5 subfamily T member 3 [Source:HGNC Symbol;Acc:HGNC:15297]"}, {"versioned_ensembl_gene_id":"ENSG00000217646.1","gene_symbol":"HIST1H2BPS2","gene_name":"histone cluster 1 H2B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4754]","synonyms":"pH2B/i,H2BFIP","biotype":"processed_pseudogene","ncbi_id":"10340","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This histone pseudogene is found in the small histone gene cluster on chromosome 6. [provided by RefSeq, Oct 2015]","start":27864062,"end":27864401,"strand":-1,"description":"histone cluster 1 H2B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4754]"}, {"versioned_ensembl_gene_id":"ENSG00000100211.10","gene_symbol":"CBY1","gene_name":"chibby family member 1, beta catenin antagonist [Source:HGNC Symbol;Acc:HGNC:1307]","synonyms":"PIGEA14,PIGEA-14,PGEA1,Chibby,Cby,C22orf2","biotype":"protein_coding","ncbi_id":"25776","summary":"Beta-catenin is a transcriptional activator and oncoprotein involved in the development of several cancers. The protein encoded by this gene interacts directly with the C-terminal region of beta-catenin, inhibiting oncogenic beta-catenin-mediated transcriptional activation by competing with transcription factors for binding to beta-catenin. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":38656636,"end":38673854,"strand":1,"description":"chibby family member 1, beta catenin antagonist [Source:HGNC Symbol;Acc:HGNC:1307]"}, {"versioned_ensembl_gene_id":"ENSG00000258282.2","gene_symbol":"AL121766.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28673241,"end":28673727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276368.1","gene_symbol":"HIST1H2AJ","gene_name":"histone cluster 1 H2A family member j [Source:HGNC Symbol;Acc:HGNC:4727]","synonyms":"H2AFE,H2A/E","biotype":"protein_coding","ncbi_id":"8331","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27814354,"end":27814740,"strand":-1,"description":"histone cluster 1 H2A family member j [Source:HGNC Symbol;Acc:HGNC:4727]"}, {"versioned_ensembl_gene_id":"ENSG00000102030.15","gene_symbol":"NAA10","gene_name":"N(alpha)-acetyltransferase 10, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:18704]","synonyms":"ARD1,TE2,DXS707,ARD1A","biotype":"protein_coding","ncbi_id":"8260","summary":"N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":153929242,"end":153935223,"strand":-1,"description":"N(alpha)-acetyltransferase 10, NatA catalytic subunit [Source:HGNC Symbol;Acc:HGNC:18704]"}, {"versioned_ensembl_gene_id":"ENSG00000281321.1","gene_symbol":"LINC02197","gene_name":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724392","summary":null,"start":70677171,"end":70771675,"strand":-1,"description":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]"}, {"versioned_ensembl_gene_id":"ENSG00000262784.2","gene_symbol":"OR5T1","gene_name":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]","synonyms":"OR5T1P","biotype":"protein_coding","ncbi_id":"390155","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56275639,"end":56276619,"strand":1,"description":"olfactory receptor family 5 subfamily T member 1 [Source:HGNC Symbol;Acc:HGNC:14821]"}, {"versioned_ensembl_gene_id":"ENSG00000271235.1","gene_symbol":"AC114477.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22811390,"end":22812047,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280840.2","gene_symbol":"PMCHL2","gene_name":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5370","summary":null,"start":70701100,"end":70711308,"strand":1,"description":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]"}, {"versioned_ensembl_gene_id":"ENSG00000275221.1","gene_symbol":"HIST1H2AK","gene_name":"histone cluster 1 H2A family member k [Source:HGNC Symbol;Acc:HGNC:4726]","synonyms":"H2AFD,H2A/d","biotype":"protein_coding","ncbi_id":"8330","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27837947,"end":27838339,"strand":-1,"description":"histone cluster 1 H2A family member k [Source:HGNC Symbol;Acc:HGNC:4726]"}, {"versioned_ensembl_gene_id":"ENSG00000282742.1","gene_symbol":"AC093323.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6697861,"end":6698809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226183.1","gene_symbol":"RANP7","gene_name":"RAN, member RAS oncogene family pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874192","summary":null,"start":22904135,"end":22905151,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39862]"}, {"versioned_ensembl_gene_id":"ENSG00000277982.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54877123,"end":54893917,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000130304.16","gene_symbol":"SLC27A1","gene_name":"solute carrier family 27 member 1 [Source:HGNC Symbol;Acc:HGNC:10995]","synonyms":"MGC71751,FLJ00336,FATP1,FATP,ACSVL5","biotype":"protein_coding","ncbi_id":"376497","summary":null,"start":17468769,"end":17506168,"strand":1,"description":"solute carrier family 27 member 1 [Source:HGNC Symbol;Acc:HGNC:10995]"}, {"versioned_ensembl_gene_id":"ENSG00000197238.4","gene_symbol":"HIST1H4J","gene_name":"histone cluster 1 H4 family member j [Source:HGNC Symbol;Acc:HGNC:4785]","synonyms":"H4FE,H4F2iv,H4/e","biotype":"protein_coding","ncbi_id":"8363","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27824108,"end":27824480,"strand":1,"description":"histone cluster 1 H4 family member j [Source:HGNC Symbol;Acc:HGNC:4785]"}, {"versioned_ensembl_gene_id":"ENSG00000231915.2","gene_symbol":"SALL4P5","gene_name":"spalt like transcription factor 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39822]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100130785","summary":null,"start":22989823,"end":22991582,"strand":1,"description":"spalt like transcription factor 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39822]"}, {"versioned_ensembl_gene_id":"ENSG00000256913.1","gene_symbol":"AC005840.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6477714,"end":6480207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262611.4","gene_symbol":"OR8H1","gene_name":"olfactory receptor family 8 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14824]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219469","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56290053,"end":56291090,"strand":-1,"description":"olfactory receptor family 8 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:14824]"}, {"versioned_ensembl_gene_id":"ENSG00000215016.2","gene_symbol":"RPL24P7","gene_name":"ribosomal protein L24 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36862]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270963","summary":null,"start":23134372,"end":23134824,"strand":1,"description":"ribosomal protein L24 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36862]"}, {"versioned_ensembl_gene_id":"ENSG00000272417.1","gene_symbol":"AC034229.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10203600,"end":10204040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122122.9","gene_symbol":"SASH3","gene_name":"SAM and SH3 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15975]","synonyms":"SLY,SH3D6C,HACS2,CXorf9,753P9","biotype":"protein_coding","ncbi_id":"54440","summary":"The protein encoded by this gene contains a Src homology-3 (SH3) domain and a sterile alpha motif (SAM), both of which are found in proteins involved in cell signaling. This protein may function as a signaling adapter protein in lymphocytes.[provided by RefSeq, Sep 2009]","start":129779979,"end":129795201,"strand":1,"description":"SAM and SH3 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:15975]"}, {"versioned_ensembl_gene_id":"ENSG00000206561.12","gene_symbol":"COLQ","gene_name":"collagen like tail subunit of asymmetric acetylcholinesterase [Source:HGNC Symbol;Acc:HGNC:2226]","synonyms":"EAD","biotype":"protein_coding","ncbi_id":"8292","summary":"This gene encodes the subunit of a collagen-like molecule associated with acetylcholinesterase in skeletal muscle. Each molecule is composed of three identical subunits. Each subunit contains a proline-rich attachment domain (PRAD) that binds an acetylcholinesterase tetramer to anchor the catalytic subunit of the enzyme to the basal lamina. Mutations in this gene are associated with endplate acetylcholinesterase deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":15450133,"end":15521751,"strand":-1,"description":"collagen like tail subunit of asymmetric acetylcholinesterase [Source:HGNC Symbol;Acc:HGNC:2226]"}, {"versioned_ensembl_gene_id":"ENSG00000280619.1","gene_symbol":"AC245931.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70770949,"end":70771902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275126.1","gene_symbol":"HIST1H4L","gene_name":"histone cluster 1 H4 family member l [Source:HGNC Symbol;Acc:HGNC:4791]","synonyms":"H4FK,H4/k,H4.k","biotype":"protein_coding","ncbi_id":"8368","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27873199,"end":27873510,"strand":-1,"description":"histone cluster 1 H4 family member l [Source:HGNC Symbol;Acc:HGNC:4791]"}, {"versioned_ensembl_gene_id":"ENSG00000262748.1","gene_symbol":"AC207056.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41384972,"end":41389707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184357.4","gene_symbol":"HIST1H1B","gene_name":"histone cluster 1 H1 family member b [Source:HGNC Symbol;Acc:HGNC:4719]","synonyms":"H1s-3,H1F5,H1b,H1.5","biotype":"protein_coding","ncbi_id":"3009","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27866849,"end":27867529,"strand":-1,"description":"histone cluster 1 H1 family member b [Source:HGNC Symbol;Acc:HGNC:4719]"}, {"versioned_ensembl_gene_id":"ENSG00000281210.1","gene_symbol":"AC245931.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70697990,"end":70700212,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178988.10","gene_symbol":"MRFAP1L1","gene_name":"Morf4 family associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28796]","synonyms":"MGC9651","biotype":"protein_coding","ncbi_id":"114932","summary":null,"start":6707701,"end":6709880,"strand":-1,"description":"Morf4 family associated protein 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28796]"}, {"versioned_ensembl_gene_id":"ENSG00000197153.4","gene_symbol":"HIST1H3J","gene_name":"histone cluster 1 H3 family member j [Source:HGNC Symbol;Acc:HGNC:4774]","synonyms":"H3FJ,H3/j","biotype":"protein_coding","ncbi_id":"8356","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27890382,"end":27893106,"strand":-1,"description":"histone cluster 1 H3 family member j [Source:HGNC Symbol;Acc:HGNC:4774]"}, {"versioned_ensembl_gene_id":"ENSG00000262148.1","gene_symbol":"RPS5P3","gene_name":"ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10427]","synonyms":"RPS5L","biotype":"processed_pseudogene","ncbi_id":"54022","summary":null,"start":33491137,"end":33491752,"strand":-1,"description":"ribosomal protein S5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:10427]"}, {"versioned_ensembl_gene_id":"ENSG00000255819.7","gene_symbol":"KLRC4-KLRK1","gene_name":"KLRC4-KLRK1 readthrough [Source:HGNC Symbol;Acc:HGNC:48357]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528032","summary":"This locus represents naturally occurring read-through transcription between the neighboring KLRC4 (killer cell lectin-like receptor subfamily C, member 4) and KLRK1 (killer cell lectin-like receptor subfamily K, member 1) genes on chromosome 12. The read-through transcript includes an alternate 5' exon and lacks a significant portion of the KLRC4 coding sequence, including the start codon, and it thus encodes the KLRK1 protein. [provided by RefSeq, Dec 2010]","start":10372353,"end":10410146,"strand":-1,"description":"KLRC4-KLRK1 readthrough [Source:HGNC Symbol;Acc:HGNC:48357]"}, {"versioned_ensembl_gene_id":"ENSG00000248968.1","gene_symbol":"AC012640.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10248325,"end":10249915,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150756.13","gene_symbol":"FAM173B","gene_name":"family with sequence similarity 173 member B [Source:HGNC Symbol;Acc:HGNC:27029]","synonyms":"JS-2","biotype":"protein_coding","ncbi_id":"134145","summary":null,"start":10226330,"end":10249897,"strand":-1,"description":"family with sequence similarity 173 member B [Source:HGNC Symbol;Acc:HGNC:27029]"}, {"versioned_ensembl_gene_id":"ENSG00000263314.1","gene_symbol":"AC207981.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33492056,"end":33493815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269019.1","gene_symbol":"AC002985.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18940322,"end":18946831,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273703.1","gene_symbol":"HIST1H2BM","gene_name":"histone cluster 1 H2B family member m [Source:HGNC Symbol;Acc:HGNC:4750]","synonyms":"H2BFE,H2B/e,dJ160A22.3","biotype":"protein_coding","ncbi_id":"8342","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27815044,"end":27815424,"strand":1,"description":"histone cluster 1 H2B family member m [Source:HGNC Symbol;Acc:HGNC:4750]"}, {"versioned_ensembl_gene_id":"ENSG00000280712.1","gene_symbol":"OR8I1P","gene_name":"olfactory receptor family 8 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14828]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79498","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56296541,"end":56297471,"strand":-1,"description":"olfactory receptor family 8 subfamily I member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14828]"}, {"versioned_ensembl_gene_id":"ENSG00000240342.3","gene_symbol":"AC026366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":118246084,"end":118246962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105669.13","gene_symbol":"COPE","gene_name":"coatomer protein complex subunit epsilon [Source:HGNC Symbol;Acc:HGNC:2234]","synonyms":"epsilon-COP","biotype":"protein_coding","ncbi_id":"11316","summary":"The product of this gene is an epsilon subunit of coatomer protein complex. Coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles. It is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. Coatomer complex consists of at least the alpha, beta, beta', gamma, delta, epsilon and zeta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":18899514,"end":18919397,"strand":-1,"description":"coatomer protein complex subunit epsilon [Source:HGNC Symbol;Acc:HGNC:2234]"}, {"versioned_ensembl_gene_id":"ENSG00000203965.12","gene_symbol":"EFCAB7","gene_name":"EF-hand calcium binding domain 7 [Source:HGNC Symbol;Acc:HGNC:29379]","synonyms":"RP4-534K7.1,KIAA1799","biotype":"protein_coding","ncbi_id":"84455","summary":null,"start":63523372,"end":63572693,"strand":1,"description":"EF-hand calcium binding domain 7 [Source:HGNC Symbol;Acc:HGNC:29379]"}, {"versioned_ensembl_gene_id":"ENSG00000186222.4","gene_symbol":"BLOC1S4","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:24206]","synonyms":"FLJ11230,CNO,BCAS4L","biotype":"protein_coding","ncbi_id":"55330","summary":"This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. A similar protein in mouse is a component of a protein complex termed biogenesis of lysosome-related organelles complex 1 (BLOC-1), and is a model for Hermansky-Pudlak syndrome. The encoded protein may play a role in intracellular vesicular trafficking. [provided by RefSeq, Jul 2008]","start":6716055,"end":6717671,"strand":1,"description":"biogenesis of lysosomal organelles complex 1 subunit 4 [Source:HGNC Symbol;Acc:HGNC:24206]"}, {"versioned_ensembl_gene_id":"ENSG00000278677.1","gene_symbol":"HIST1H2AM","gene_name":"histone cluster 1 H2A family member m [Source:HGNC Symbol;Acc:HGNC:4735]","synonyms":"H2AFN,H2A/n,H2A.1","biotype":"protein_coding","ncbi_id":"8336","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27892757,"end":27893149,"strand":-1,"description":"histone cluster 1 H2A family member m [Source:HGNC Symbol;Acc:HGNC:4735]"}, {"versioned_ensembl_gene_id":"ENSG00000205944.11","gene_symbol":"DAZ2","gene_name":"deleted in azoospermia 2 [Source:HGNC Symbol;Acc:HGNC:15964]","synonyms":"pDP1678,MGC126442","biotype":"protein_coding","ncbi_id":"57055","summary":"This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains one copy of the 10.8 kb repeat. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":23219434,"end":23291356,"strand":1,"description":"deleted in azoospermia 2 [Source:HGNC Symbol;Acc:HGNC:15964]"}, {"versioned_ensembl_gene_id":"ENSG00000233153.5","gene_symbol":"UBE2E2-AS1","gene_name":"UBE2E2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44512]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505877","summary":null,"start":23195070,"end":23202578,"strand":-1,"description":"UBE2E2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44512]"}, {"versioned_ensembl_gene_id":"ENSG00000262755.1","gene_symbol":"OR8K3","gene_name":"olfactory receptor family 8 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15313]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"219473","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":56318307,"end":56319245,"strand":1,"description":"olfactory receptor family 8 subfamily K member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15313]"}, {"versioned_ensembl_gene_id":"ENSG00000269025.2","gene_symbol":"AC011467.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":22605739,"end":22608211,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072401.14","gene_symbol":"UBE2D1","gene_name":"ubiquitin conjugating enzyme E2 D1 [Source:HGNC Symbol;Acc:HGNC:12474]","synonyms":"UbcH5A,UBCH5,UBC4/5,SFT,E2(17)KB1","biotype":"protein_coding","ncbi_id":"7321","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is closely related to a stimulator of iron transport (SFT), and is up-regulated in hereditary hemochromatosis. It also functions in the ubiquitination of the tumor-suppressor protein p53 and the hypoxia-inducible transcription factor HIF1alpha by interacting with the E1 ubiquitin-activating enzyme and the E3 ubiquitin-protein ligases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","start":58334975,"end":58370753,"strand":1,"description":"ubiquitin conjugating enzyme E2 D1 [Source:HGNC Symbol;Acc:HGNC:12474]"}, {"versioned_ensembl_gene_id":"ENSG00000268038.1","gene_symbol":"LINC01785","gene_name":"long intergenic non-protein coding RNA 1785 [Source:HGNC Symbol;Acc:HGNC:25060]","synonyms":null,"biotype":"lincRNA","ncbi_id":"374890","summary":null,"start":22615557,"end":22623971,"strand":-1,"description":"long intergenic non-protein coding RNA 1785 [Source:HGNC Symbol;Acc:HGNC:25060]"}, {"versioned_ensembl_gene_id":"ENSG00000281773.1","gene_symbol":"FAM8A2P","gene_name":"family with sequence similarity 8 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:16373]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728097","summary":null,"start":56331347,"end":56332488,"strand":-1,"description":"family with sequence similarity 8 member A2, pseudogene [Source:HGNC Symbol;Acc:HGNC:16373]"}, {"versioned_ensembl_gene_id":"ENSG00000137944.17","gene_symbol":"KYAT3","gene_name":"kynurenine aminotransferase 3 [Source:HGNC Symbol;Acc:HGNC:33238]","synonyms":"RP11-82K18.3,RBM1,KATIII,KAT3,CCBL2","biotype":"protein_coding","ncbi_id":"56267","summary":"This gene encodes an aminotransferase that transaminates kynurenine to form kynurenic acid, which is a metabolite of tryptophan. Multiple alternatively spliced transcript variants that encode different proteins have been described for this gene. This gene shares 5' exon structure with the RNA binding motif protein, X-linked-like 1 locus on chromosome 1, but the coding sequences are non-overlapping. [provided by RefSeq, Mar 2017]","start":88935773,"end":88992953,"strand":-1,"description":"kynurenine aminotransferase 3 [Source:HGNC Symbol;Acc:HGNC:33238]"}, {"versioned_ensembl_gene_id":"ENSG00000273542.1","gene_symbol":"HIST1H4K","gene_name":"histone cluster 1 H4 family member k [Source:HGNC Symbol;Acc:HGNC:4784]","synonyms":"H4FD,H4F2iii,H4/d,dJ160A22.1","biotype":"protein_coding","ncbi_id":"8362","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H4 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27831216,"end":27831527,"strand":-1,"description":"histone cluster 1 H4 family member k [Source:HGNC Symbol;Acc:HGNC:4784]"}, {"versioned_ensembl_gene_id":"ENSG00000274958.4","gene_symbol":"ITPK1","gene_name":"inositol-tetrakisphosphate 1-kinase [Source:HGNC Symbol;Acc:HGNC:6177]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3705","summary":"This gene encodes an enzyme that belongs to the inositol 1,3,4-trisphosphate 5/6-kinase family. This enzyme regulates the synthesis of inositol tetraphosphate, and downstream products, inositol pentakisphosphate and inositol hexakisphosphate. Inositol metabolism plays a role in the development of the neural tube. Disruptions in this gene are thought to be associated with neural tube defects. A pseudogene of this gene has been identified on chromosome X. [provided by RefSeq, Jul 2016]","start":92936914,"end":93116320,"strand":-1,"description":"inositol-tetrakisphosphate 1-kinase [Source:HGNC Symbol;Acc:HGNC:6177]"}, {"versioned_ensembl_gene_id":"ENSG00000267063.1","gene_symbol":"AC006130.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2847227,"end":2858716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230844.2","gene_symbol":"ZNF674-AS1","gene_name":"ZNF674 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44266]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401588","summary":null,"start":46545493,"end":46548408,"strand":1,"description":"ZNF674 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:44266]"}, {"versioned_ensembl_gene_id":"ENSG00000276903.1","gene_symbol":"HIST1H2AL","gene_name":"histone cluster 1 H2A family member l [Source:HGNC Symbol;Acc:HGNC:4730]","synonyms":"H2AFI,H2A/i,dJ193B12.9","biotype":"protein_coding","ncbi_id":"8332","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27865355,"end":27865747,"strand":1,"description":"histone cluster 1 H2A family member l [Source:HGNC Symbol;Acc:HGNC:4730]"}, {"versioned_ensembl_gene_id":"ENSG00000197360.9","gene_symbol":"ZNF98","gene_name":"zinc finger protein 98 [Source:HGNC Symbol;Acc:HGNC:13174]","synonyms":"ZNF739,F7175","biotype":"protein_coding","ncbi_id":"148198","summary":null,"start":22391019,"end":22532485,"strand":-1,"description":"zinc finger protein 98 [Source:HGNC Symbol;Acc:HGNC:13174]"}, {"versioned_ensembl_gene_id":"ENSG00000186300.11","gene_symbol":"ZNF555","gene_name":"zinc finger protein 555 [Source:HGNC Symbol;Acc:HGNC:28382]","synonyms":"MGC26707","biotype":"protein_coding","ncbi_id":"148254","summary":null,"start":2841435,"end":2860484,"strand":1,"description":"zinc finger protein 555 [Source:HGNC Symbol;Acc:HGNC:28382]"}, {"versioned_ensembl_gene_id":"ENSG00000275379.1","gene_symbol":"HIST1H3I","gene_name":"histone cluster 1 H3 family member i [Source:HGNC Symbol;Acc:HGNC:4771]","synonyms":"H3FF,H3/f,H3.f","biotype":"protein_coding","ncbi_id":"8354","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27871905,"end":27872315,"strand":-1,"description":"histone cluster 1 H3 family member i [Source:HGNC Symbol;Acc:HGNC:4771]"}, {"versioned_ensembl_gene_id":"ENSG00000280617.1","gene_symbol":"OR8K2P","gene_name":"olfactory receptor family 8 subfamily K member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14832]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"79494","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56335142,"end":56336068,"strand":1,"description":"olfactory receptor family 8 subfamily K member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:14832]"}, {"versioned_ensembl_gene_id":"ENSG00000262045.1","gene_symbol":"KRT34","gene_name":"keratin 34 [Source:HGNC Symbol;Acc:HGNC:6452]","synonyms":"Ha-4,KRTHA4","biotype":"protein_coding","ncbi_id":"3885","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41377665,"end":41382400,"strand":-1,"description":"keratin 34 [Source:HGNC Symbol;Acc:HGNC:6452]"}, {"versioned_ensembl_gene_id":"ENSG00000170871.11","gene_symbol":"KIAA0232","gene_name":"KIAA0232 [Source:HGNC Symbol;Acc:HGNC:28992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9778","summary":null,"start":6781375,"end":6884170,"strand":1,"description":"KIAA0232 [Source:HGNC Symbol;Acc:HGNC:28992]"}, {"versioned_ensembl_gene_id":"ENSG00000206471.10","gene_symbol":"OR2H1","gene_name":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]","synonyms":"OR2H8,OR2H6,OR6-2","biotype":"protein_coding","ncbi_id":"26716","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29456962,"end":29464109,"strand":1,"description":"olfactory receptor family 2 subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:8252]"}, {"versioned_ensembl_gene_id":"ENSG00000204624.7","gene_symbol":"DISP3","gene_name":"dispatched RND transporter family member 3 [Source:HGNC Symbol;Acc:HGNC:29251]","synonyms":"PTCHD2,KIAA1337","biotype":"protein_coding","ncbi_id":"57540","summary":null,"start":11479166,"end":11537584,"strand":1,"description":"dispatched RND transporter family member 3 [Source:HGNC Symbol;Acc:HGNC:29251]"}, {"versioned_ensembl_gene_id":"ENSG00000196350.8","gene_symbol":"ZNF729","gene_name":"zinc finger protein 729 [Source:HGNC Symbol;Acc:HGNC:32464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287226","summary":null,"start":22286408,"end":22317176,"strand":1,"description":"zinc finger protein 729 [Source:HGNC Symbol;Acc:HGNC:32464]"}, {"versioned_ensembl_gene_id":"ENSG00000269138.1","gene_symbol":"ZNF209P","gene_name":"zinc finger protein 209, pseudogene [Source:HGNC Symbol;Acc:HGNC:13000]","synonyms":"ZNF209","biotype":"unprocessed_pseudogene","ncbi_id":"441843","summary":null,"start":22463922,"end":22473036,"strand":1,"description":"zinc finger protein 209, pseudogene [Source:HGNC Symbol;Acc:HGNC:13000]"}, {"versioned_ensembl_gene_id":"ENSG00000228433.1","gene_symbol":"OR7E23P","gene_name":"olfactory receptor family 7 subfamily E member 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:8395]","synonyms":"OR7E92P,OR21-3","biotype":"processed_pseudogene","ncbi_id":"391279","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":32621049,"end":32622096,"strand":1,"description":"olfactory receptor family 7 subfamily E member 23 pseudogene [Source:HGNC Symbol;Acc:HGNC:8395]"}, {"versioned_ensembl_gene_id":"ENSG00000241282.1","gene_symbol":"RPL34P33","gene_name":"ribosomal protein L34 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36666]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730061","summary":null,"start":22699352,"end":22699685,"strand":1,"description":"ribosomal protein L34 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:36666]"}, {"versioned_ensembl_gene_id":"ENSG00000270499.1","gene_symbol":"MKI67P1","gene_name":"marker of proliferation Ki-67 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49230]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271918","summary":null,"start":46560928,"end":46562749,"strand":-1,"description":"marker of proliferation Ki-67 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49230]"}, {"versioned_ensembl_gene_id":"ENSG00000238220.1","gene_symbol":"AP000275.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32624416,"end":32625096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229676.2","gene_symbol":"ZNF492","gene_name":"zinc finger protein 492 [Source:HGNC Symbol;Acc:HGNC:23707]","synonyms":"ZNF115,KIAA1473","biotype":"protein_coding","ncbi_id":"57615","summary":null,"start":22634324,"end":22667670,"strand":1,"description":"zinc finger protein 492 [Source:HGNC Symbol;Acc:HGNC:23707]"}, {"versioned_ensembl_gene_id":"ENSG00000138892.11","gene_symbol":"TTLL8","gene_name":"tubulin tyrosine ligase like 8 [Source:HGNC Symbol;Acc:HGNC:34000]","synonyms":null,"biotype":"protein_coding","ncbi_id":"164714","summary":null,"start":50015123,"end":50056935,"strand":-1,"description":"tubulin tyrosine ligase like 8 [Source:HGNC Symbol;Acc:HGNC:34000]"}, {"versioned_ensembl_gene_id":"ENSG00000263012.1","gene_symbol":"KRT33B","gene_name":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]","synonyms":"KRTHA3B,Ha-3II","biotype":"protein_coding","ncbi_id":"3884","summary":"This gene encodes a member of the keratin gene family. This gene is one of multiple type I hair keratin genes that are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. As a type I hair keratin, the encoded protein is an acidic protein which heterodimerizes with type II keratins to form hair and nails. There are two isoforms of this protein, encoded by two separate genes, keratin 33A and keratin 33B. [provided by RefSeq, May 2012]","start":41363494,"end":41369800,"strand":-1,"description":"keratin 33B [Source:HGNC Symbol;Acc:HGNC:6451]"}, {"versioned_ensembl_gene_id":"ENSG00000228274.3","gene_symbol":"AL021707.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38667585,"end":38681820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135929.8","gene_symbol":"CYP27A1","gene_name":"cytochrome P450 family 27 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2605]","synonyms":"CYP27,CTX,CP27","biotype":"protein_coding","ncbi_id":"1593","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. [provided by RefSeq, Jul 2008]","start":218781749,"end":218815293,"strand":1,"description":"cytochrome P450 family 27 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2605]"}, {"versioned_ensembl_gene_id":"ENSG00000271608.1","gene_symbol":"AL391646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108551018,"end":108551207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268717.1","gene_symbol":"BNIP3P33","gene_name":"BCL2 interacting protein 3 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49713]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481695","summary":null,"start":22457329,"end":22458212,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49713]"}, {"versioned_ensembl_gene_id":"ENSG00000268823.2","gene_symbol":"AC011467.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22603269,"end":22608501,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270191.1","gene_symbol":"BNIP3P31","gene_name":"BCL2 interacting protein 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480282","summary":null,"start":22298977,"end":22299868,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49711]"}, {"versioned_ensembl_gene_id":"ENSG00000268589.1","gene_symbol":"AC011467.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22620483,"end":22620724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268830.1","gene_symbol":"BNIP3P32","gene_name":"BCL2 interacting protein 3 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49712]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480283","summary":null,"start":22447934,"end":22448777,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:49712]"}, {"versioned_ensembl_gene_id":"ENSG00000118689.14","gene_symbol":"FOXO3","gene_name":"forkhead box O3 [Source:HGNC Symbol;Acc:HGNC:3821]","synonyms":"FOXO3A,FOXO2,FKHRL1,AF6q21","biotype":"protein_coding","ncbi_id":"2309","summary":"This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. This gene likely functions as a trigger for apoptosis through expression of genes necessary for cell death. Translocation of this gene with the MLL gene is associated with secondary acute leukemia. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":108559835,"end":108684774,"strand":1,"description":"forkhead box O3 [Source:HGNC Symbol;Acc:HGNC:3821]"}, {"versioned_ensembl_gene_id":"ENSG00000270317.1","gene_symbol":"AC004004.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22501699,"end":22501948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277895.1","gene_symbol":"AC135279.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64451591,"end":64452901,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270947.1","gene_symbol":"AC025811.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22455988,"end":22456459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234772.1","gene_symbol":"LINC00412","gene_name":"long intergenic non-protein coding RNA 412 [Source:HGNC Symbol;Acc:HGNC:42745]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723332","summary":null,"start":27236282,"end":27236811,"strand":-1,"description":"long intergenic non-protein coding RNA 412 [Source:HGNC Symbol;Acc:HGNC:42745]"}, {"versioned_ensembl_gene_id":"ENSG00000269364.1","gene_symbol":"LINC01233","gene_name":"long intergenic non-protein coding RNA 1233 [Source:HGNC Symbol;Acc:HGNC:49756]","synonyms":"XLOC_013014","biotype":"lincRNA","ncbi_id":"100128139","summary":null,"start":22532626,"end":22533494,"strand":1,"description":"long intergenic non-protein coding RNA 1233 [Source:HGNC Symbol;Acc:HGNC:49756]"}, {"versioned_ensembl_gene_id":"ENSG00000183735.9","gene_symbol":"TBK1","gene_name":"TANK binding kinase 1 [Source:HGNC Symbol;Acc:HGNC:11584]","synonyms":"NAK","biotype":"protein_coding","ncbi_id":"29110","summary":"The NF-kappa-B (NFKB) complex of proteins is inhibited by I-kappa-B (IKB) proteins, which inactivate NFKB by trapping it in the cytoplasm. Phosphorylation of serine residues on the IKB proteins by IKB kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation and nuclear translocation of the NFKB complex. The protein encoded by this gene is similar to IKB kinases and can mediate NFKB activation in response to certain growth factors. [provided by RefSeq, Oct 2010]","start":64451880,"end":64502108,"strand":1,"description":"TANK binding kinase 1 [Source:HGNC Symbol;Acc:HGNC:11584]"}, {"versioned_ensembl_gene_id":"ENSG00000230641.1","gene_symbol":"USP12-AS2","gene_name":"USP12 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:39962]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874071","summary":null,"start":27172259,"end":27182998,"strand":1,"description":"USP12 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:39962]"}, {"versioned_ensembl_gene_id":"ENSG00000275294.4","gene_symbol":"LINC02340","gene_name":"long intergenic non-protein coding RNA 2340 [Source:HGNC Symbol;Acc:HGNC:53260]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370125","summary":null,"start":27178263,"end":27251288,"strand":-1,"description":"long intergenic non-protein coding RNA 2340 [Source:HGNC Symbol;Acc:HGNC:53260]"}, {"versioned_ensembl_gene_id":"ENSG00000269316.1","gene_symbol":"AC011467.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22609606,"end":22610601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179023.8","gene_symbol":"KLHDC7A","gene_name":"kelch domain containing 7A [Source:HGNC Symbol;Acc:HGNC:26791]","synonyms":"FLJ38753","biotype":"protein_coding","ncbi_id":"127707","summary":null,"start":18480982,"end":18486126,"strand":1,"description":"kelch domain containing 7A [Source:HGNC Symbol;Acc:HGNC:26791]"}, {"versioned_ensembl_gene_id":"ENSG00000271149.1","gene_symbol":"AC011467.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22595479,"end":22596163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147119.3","gene_symbol":"CHST7","gene_name":"carbohydrate sulfotransferase 7 [Source:HGNC Symbol;Acc:HGNC:13817]","synonyms":"C6ST2,C6ST-2","biotype":"protein_coding","ncbi_id":"56548","summary":"This gene is a member of the Gal/GalNAc/GlcNAc (galactose/N-acetylgalactosamine/N-acetylglucosamine) 6-O-sulfotransferase (GST) family. Members of this family encode enzymes that catalyze the specific addition of sulfate groups to distinct hydroxyl and amino groups of carbohydrates. The encoded protein catalyzes the sulfation of 6-hydroxyl group of GalNAc in chondroitin. [provided by RefSeq, Aug 2013]","start":46573784,"end":46598408,"strand":1,"description":"carbohydrate sulfotransferase 7 [Source:HGNC Symbol;Acc:HGNC:13817]"}, {"versioned_ensembl_gene_id":"ENSG00000263328.2","gene_symbol":"OR8K1","gene_name":"olfactory receptor family 8 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14831]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390157","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56346039,"end":56346998,"strand":1,"description":"olfactory receptor family 8 subfamily K member 1 [Source:HGNC Symbol;Acc:HGNC:14831]"}, {"versioned_ensembl_gene_id":"ENSG00000269332.5","gene_symbol":"GOLGA2P9","gene_name":"golgin A2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49921]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440518","summary":null,"start":22596257,"end":22603550,"strand":1,"description":"golgin A2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:49921]"}, {"versioned_ensembl_gene_id":"ENSG00000271754.1","gene_symbol":"AL355802.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43519180,"end":43519724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281820.1","gene_symbol":"RPL5P29","gene_name":"ribosomal protein L5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36335]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390158","summary":null,"start":56357328,"end":56358221,"strand":1,"description":"ribosomal protein L5 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:36335]"}, {"versioned_ensembl_gene_id":"ENSG00000219470.1","gene_symbol":"AL355802.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43538822,"end":43539703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257510.1","gene_symbol":"LINC02402","gene_name":"long intergenic non-protein coding RNA 2402 [Source:HGNC Symbol;Acc:HGNC:53329]","synonyms":"ENST00000550337.1","biotype":"lincRNA","ncbi_id":"101927058","summary":null,"start":42615503,"end":42646498,"strand":-1,"description":"long intergenic non-protein coding RNA 2402 [Source:HGNC Symbol;Acc:HGNC:53329]"}, {"versioned_ensembl_gene_id":"ENSG00000204052.4","gene_symbol":"LRRC73","gene_name":"leucine rich repeat containing 73 [Source:HGNC Symbol;Acc:HGNC:21375]","synonyms":"dJ337H4.2,C6orf154","biotype":"protein_coding","ncbi_id":"221424","summary":null,"start":43506969,"end":43510686,"strand":-1,"description":"leucine rich repeat containing 73 [Source:HGNC Symbol;Acc:HGNC:21375]"}, {"versioned_ensembl_gene_id":"ENSG00000262796.1","gene_symbol":"OR8J1","gene_name":"olfactory receptor family 8 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:14855]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219477","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56360215,"end":56361288,"strand":1,"description":"olfactory receptor family 8 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:14855]"}, {"versioned_ensembl_gene_id":"ENSG00000250379.1","gene_symbol":"AC020659.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41825099,"end":41827936,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228976.1","gene_symbol":"SUMO2P8","gene_name":"SUMO2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100506244","summary":null,"start":108618000,"end":108618285,"strand":-1,"description":"SUMO2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39018]"}, {"versioned_ensembl_gene_id":"ENSG00000257405.1","gene_symbol":"AC079600.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42636815,"end":42637111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156973.13","gene_symbol":"PDE6D","gene_name":"phosphodiesterase 6D [Source:HGNC Symbol;Acc:HGNC:8788]","synonyms":"JBTS22","biotype":"protein_coding","ncbi_id":"5147","summary":"This gene encodes the delta subunit of rod-specific photoreceptor phosphodiesterase (PDE), a key enzyme in the phototransduction cascade. A similar protein in cow functions in solubilizing membrane-bound PDE. In addition to its role in the PDE complex, the encoded protein is thought to bind to prenyl groups of proteins to target them to subcellular organelles called cilia. Mutations in this gene are associated with Joubert syndrome-22. Alternative splicing results in multiple splice variants. [provided by RefSeq, Mar 2014]","start":231732425,"end":231786272,"strand":-1,"description":"phosphodiesterase 6D [Source:HGNC Symbol;Acc:HGNC:8788]"}, {"versioned_ensembl_gene_id":"ENSG00000240143.1","gene_symbol":"AL023653.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":129794994,"end":129796963,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253275.1","gene_symbol":"AC068672.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31497423,"end":31498612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257687.1","gene_symbol":"AC079600.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42627008,"end":42627137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260575.1","gene_symbol":"AC133485.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32250620,"end":32254422,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269796.1","gene_symbol":"AC011516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22422513,"end":22426045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233838.5","gene_symbol":"DPH3P1","gene_name":"diphthamide biosynthesis 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16136]","synonyms":"ZCSL1,DPH3B,dJ885L7.5,C20orf143","biotype":"processed_pseudogene","ncbi_id":"100132911","summary":"This gene may represent a processed pseudogene of DPH3, GeneID: 285381, because it lacks the exon/intron structure found in the functional gene. It does contain an intact open reading frame but it has not been established that the predicted protein is translated. [provided by RefSeq, Nov 2020]","start":62845664,"end":62845912,"strand":1,"description":"diphthamide biosynthesis 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16136]"}, {"versioned_ensembl_gene_id":"ENSG00000237361.2","gene_symbol":"TUSC8","gene_name":"tumor suppressor candidate 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49111]","synonyms":"XLOC_010588,LINC01071","biotype":"lincRNA","ncbi_id":"400128","summary":null,"start":44400250,"end":44405984,"strand":-1,"description":"tumor suppressor candidate 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49111]"}, {"versioned_ensembl_gene_id":"ENSG00000225387.1","gene_symbol":"AL591896.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18385829,"end":18388514,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268981.5","gene_symbol":"AC024563.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22665552,"end":22716991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205456.11","gene_symbol":"TP53TG3D","gene_name":"TP53 target 3D [Source:HGNC Symbol;Acc:HGNC:44657]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729264","summary":null,"start":32252719,"end":32255922,"strand":1,"description":"TP53 target 3D [Source:HGNC Symbol;Acc:HGNC:44657]"}, {"versioned_ensembl_gene_id":"ENSG00000227039.6","gene_symbol":"ITGB2-AS1","gene_name":"ITGB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44304]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505746","summary":null,"start":44921051,"end":44929678,"strand":1,"description":"ITGB2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44304]"}, {"versioned_ensembl_gene_id":"ENSG00000101190.12","gene_symbol":"TCFL5","gene_name":"transcription factor like 5 [Source:HGNC Symbol;Acc:HGNC:11646]","synonyms":"Figlb,E2BP-1,CHA,bHLHe82","biotype":"protein_coding","ncbi_id":"10732","summary":null,"start":62841115,"end":62861763,"strand":-1,"description":"transcription factor like 5 [Source:HGNC Symbol;Acc:HGNC:11646]"}, {"versioned_ensembl_gene_id":"ENSG00000213672.7","gene_symbol":"NCKIPSD","gene_name":"NCK interacting protein with SH3 domain [Source:HGNC Symbol;Acc:HGNC:15486]","synonyms":"WISH,WASLBP,SPIN90,ORF1,DIP1,AF3P21","biotype":"protein_coding","ncbi_id":"51517","summary":"The protein encoded by this gene contains a nuclear localization signal. It plays a role in signal transduction, and may function in the maintenance of sarcomeres and in the assembly of myofibrils into sarcomeres. It also plays an important role in stress fiber formation This protein is involved in the formation and maintenance of dendritic spines, and modulates synaptic activity in neurons. The gene is involved in therapy-related leukemia by a chromosomal translocation t(3;11)(p21;q23) that involves this gene and the myeloid/lymphoid leukemia gene. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2019]","start":48673844,"end":48686364,"strand":-1,"description":"NCK interacting protein with SH3 domain [Source:HGNC Symbol;Acc:HGNC:15486]"}, {"versioned_ensembl_gene_id":"ENSG00000224578.4","gene_symbol":"HNRNPA1P48","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48778]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"642659","summary":null,"start":51645756,"end":51647132,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:48778]"}, {"versioned_ensembl_gene_id":"ENSG00000238021.6","gene_symbol":"ARMC4P1","gene_name":"armadillo repeat containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44937]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101060171","summary":null,"start":27258762,"end":27288824,"strand":1,"description":"armadillo repeat containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44937]"}, {"versioned_ensembl_gene_id":"ENSG00000225478.2","gene_symbol":"AL031737.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18595414,"end":18595636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270475.1","gene_symbol":"AC024563.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22708834,"end":22709314,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236312.3","gene_symbol":"RPL34P34","gene_name":"ribosomal protein L34 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35848]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"342994","summary":null,"start":22368599,"end":22368952,"strand":-1,"description":"ribosomal protein L34 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:35848]"}, {"versioned_ensembl_gene_id":"ENSG00000273027.1","gene_symbol":"AL844908.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44929653,"end":44930112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230445.4","gene_symbol":"LRRC37A6P","gene_name":"leucine rich repeat containing 37 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:33746]","synonyms":"LRRC37E","biotype":"transcribed_processed_pseudogene","ncbi_id":"387646","summary":null,"start":27246350,"end":27259455,"strand":-1,"description":"leucine rich repeat containing 37 member A6, pseudogene [Source:HGNC Symbol;Acc:HGNC:33746]"}, {"versioned_ensembl_gene_id":"ENSG00000282071.1","gene_symbol":"AC069363.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36012540,"end":36012927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101412.12","gene_symbol":"E2F1","gene_name":"E2F transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3113]","synonyms":"RBP3,RBBP3","biotype":"protein_coding","ncbi_id":"1869","summary":"The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein and another 2 members, E2F2 and E2F3, have an additional cyclin binding domain. This protein binds preferentially to retinoblastoma protein pRB in a cell-cycle dependent manner. It can mediate both cell proliferation and p53-dependent/independent apoptosis. [provided by RefSeq, Jul 2008]","start":33675683,"end":33686404,"strand":-1,"description":"E2F transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3113]"}, {"versioned_ensembl_gene_id":"ENSG00000122367.19","gene_symbol":"LDB3","gene_name":"LIM domain binding 3 [Source:HGNC Symbol;Acc:HGNC:15710]","synonyms":"ZASP,PDLIM6,KIAA0613,CMD1C","biotype":"protein_coding","ncbi_id":"11155","summary":"This gene encodes a PDZ domain-containing protein. PDZ motifs are modular protein-protein interaction domains consisting of 80-120 amino acid residues. PDZ domain-containing proteins interact with each other in cytoskeletal assembly or with other proteins involved in targeting and clustering of membrane proteins. The protein encoded by this gene interacts with alpha-actinin-2 through its N-terminal PDZ domain and with protein kinase C via its C-terminal LIM domains. The LIM domain is a cysteine-rich motif defined by 50-60 amino acids containing two zinc-binding modules. This protein also interacts with all three members of the myozenin family. Mutations in this gene have been associated with myofibrillar myopathy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding different isoforms have been identified; all isoforms have N-terminal PDZ domains while only longer isoforms (1, 2 and 5) have C-terminal LIM domains. [provided by RefSeq, Jan 2010]","start":86668449,"end":86736068,"strand":1,"description":"LIM domain binding 3 [Source:HGNC Symbol;Acc:HGNC:15710]"}, {"versioned_ensembl_gene_id":"ENSG00000275088.1","gene_symbol":"AC026469.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85142696,"end":85146001,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142856.16","gene_symbol":"ITGB3BP","gene_name":"integrin subunit beta 3 binding protein [Source:HGNC Symbol;Acc:HGNC:6157]","synonyms":"NRIF3,HSU37139,CENPR,TAP20","biotype":"protein_coding","ncbi_id":"23421","summary":"This gene encodes a transcriptional coregulator that binds to and enhances the activity of members of the nuclear receptor families, thyroid hormone receptors and retinoid X receptors. This protein also acts as a corepressor of NF-kappaB-dependent signaling. This protein induces apoptosis in breast cancer cells through a caspase 2-mediated signaling pathway. This protein is also a component of the centromere-specific histone H3 variant nucleosome associated complex (CENP-NAC) and may be involved in mitotic progression by recruiting the histone H3 variant CENP-A to the centromere. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":63440770,"end":63593721,"strand":-1,"description":"integrin subunit beta 3 binding protein [Source:HGNC Symbol;Acc:HGNC:6157]"}, {"versioned_ensembl_gene_id":"ENSG00000160255.17","gene_symbol":"ITGB2","gene_name":"integrin subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:6155]","synonyms":"CD18,MFI7,MAC-1,LFA-1","biotype":"protein_coding","ncbi_id":"3689","summary":"This gene encodes an integrin beta chain, which combines with multiple different alpha chains to form different integrin heterodimers. Integrins are integral cell-surface proteins that participate in cell adhesion as well as cell-surface mediated signalling. The encoded protein plays an important role in immune response and defects in this gene cause leukocyte adhesion deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":44885953,"end":44931989,"strand":-1,"description":"integrin subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:6155]"}, {"versioned_ensembl_gene_id":"ENSG00000232148.1","gene_symbol":"FMO11P","gene_name":"flavin containing monooxygenase 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:32212]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100337590","summary":null,"start":166763334,"end":166792767,"strand":1,"description":"flavin containing monooxygenase 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:32212]"}, {"versioned_ensembl_gene_id":"ENSG00000100427.15","gene_symbol":"MLC1","gene_name":"megalencephalic leukoencephalopathy with subcortical cysts 1 [Source:HGNC Symbol;Acc:HGNC:17082]","synonyms":"VL,MLC,LVM,KIAA0027","biotype":"protein_coding","ncbi_id":"23209","summary":"The function of this gene product is unknown; however, homology to other proteins suggests that it may be an integral membrane transporter. Mutations in this gene have been associated with megalencephalic leukoencephalopathy with subcortical cysts, an autosomal recessive neurological disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":50059391,"end":50085902,"strand":-1,"description":"megalencephalic leukoencephalopathy with subcortical cysts 1 [Source:HGNC Symbol;Acc:HGNC:17082]"}, {"versioned_ensembl_gene_id":"ENSG00000163207.6","gene_symbol":"IVL","gene_name":"involucrin [Source:HGNC Symbol;Acc:HGNC:6187]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3713","summary":"Involucrin, a component of the keratinocyte crosslinked envelope, is found in the cytoplasm and crosslinked to membrane proteins by transglutaminase. This gene is mapped to 1q21, among calpactin I light chain, trichohyalin, profillaggrin, loricrin, and calcyclin. [provided by RefSeq, Jul 2008]","start":152908545,"end":152911886,"strand":1,"description":"involucrin [Source:HGNC Symbol;Acc:HGNC:6187]"}, {"versioned_ensembl_gene_id":"ENSG00000278214.1","gene_symbol":"LINC02139","gene_name":"long intergenic non-protein coding RNA 2139 [Source:HGNC Symbol;Acc:HGNC:52999]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400548","summary":null,"start":85137150,"end":85149443,"strand":1,"description":"long intergenic non-protein coding RNA 2139 [Source:HGNC Symbol;Acc:HGNC:52999]"}, {"versioned_ensembl_gene_id":"ENSG00000278156.1","gene_symbol":"TSC22D1-AS1","gene_name":"TSC22D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43684]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"641467","summary":null,"start":44575893,"end":44580432,"strand":1,"description":"TSC22D1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43684]"}, {"versioned_ensembl_gene_id":"ENSG00000262412.1","gene_symbol":"AL160291.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27243130,"end":27250804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248439.2","gene_symbol":"RPL23AP94","gene_name":"ribosomal protein L23a pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:51629]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481971","summary":null,"start":112530371,"end":112530672,"strand":-1,"description":"ribosomal protein L23a pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:51629]"}, {"versioned_ensembl_gene_id":"ENSG00000152147.10","gene_symbol":"GEMIN6","gene_name":"gem nuclear organelle associated protein 6 [Source:HGNC Symbol;Acc:HGNC:20044]","synonyms":"FLJ23459","biotype":"protein_coding","ncbi_id":"79833","summary":"GEMIN6 is part of a large macromolecular complex, localized to both the cytoplasm and the nucleus, that plays a role in the cytoplasmic assembly of small nuclear ribonucleoproteins (snRNPs). Other members of this complex include SMN (MIM 600354), GEMIN2 (SIP1; MIM 602595), GEMIN3 (DDX20; MIM 606168), GEMIN4 (MIM 606969), and GEMIN5 (MIM 607005).[supplied by OMIM, Jul 2002]","start":38751534,"end":38785000,"strand":1,"description":"gem nuclear organelle associated protein 6 [Source:HGNC Symbol;Acc:HGNC:20044]"}, {"versioned_ensembl_gene_id":"ENSG00000240138.1","gene_symbol":"EEF1GP4","gene_name":"eukaryotic translation elongation factor 1 gamma pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44559]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129403","summary":null,"start":161324913,"end":161326219,"strand":-1,"description":"eukaryotic translation elongation factor 1 gamma pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44559]"}, {"versioned_ensembl_gene_id":"ENSG00000232223.1","gene_symbol":"CNN2P10","gene_name":"calponin 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39535]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646693","summary":null,"start":166796266,"end":166797183,"strand":1,"description":"calponin 2 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39535]"}, {"versioned_ensembl_gene_id":"ENSG00000102804.14","gene_symbol":"TSC22D1","gene_name":"TSC22 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:16826]","synonyms":"TSC22,TGFB1I4,MGC17597","biotype":"protein_coding","ncbi_id":"8848","summary":"This gene encodes a member of the TSC22 domain family of leucine zipper transcription factors. The encoded protein is stimulated by transforming growth factor beta, and regulates the transcription of multiple genes including C-type natriuretic peptide. The encoded protein may play a critical role in tumor suppression through the induction of cancer cell apoptosis, and a single nucleotide polymorphism in the promoter of this gene has been associated with diabetic nephropathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]","start":44432143,"end":44577147,"strand":-1,"description":"TSC22 domain family member 1 [Source:HGNC Symbol;Acc:HGNC:16826]"}, {"versioned_ensembl_gene_id":"ENSG00000176165.10","gene_symbol":"FOXG1","gene_name":"forkhead box G1 [Source:HGNC Symbol;Acc:HGNC:3811]","synonyms":"FKH2,BF1,QIN,HFK3,HFK2,HFK1,HBF-3,FOXG1C,FOXG1B,FOXG1A,FKHL4,FKHL3,FKHL2,FKHL1","biotype":"protein_coding","ncbi_id":"2290","summary":"This locus encodes a member of the fork-head transcription factor family. The encoded protein, which functions as a transcriptional repressor, is highly expressed in neural tissues during brain development. Mutations at this locus have been associated with Rett syndrome and a diverse spectrum of neurodevelopmental disorders defined as part of the FOXG1 syndrome. This gene is disregulated in many types of cancer and is the target of multiple microRNAs that regulate the proliferation of tumor cells. [provided by RefSeq, Jul 2020]","start":28760330,"end":28770277,"strand":1,"description":"forkhead box G1 [Source:HGNC Symbol;Acc:HGNC:3811]"}, {"versioned_ensembl_gene_id":"ENSG00000260057.5","gene_symbol":"LINC01571","gene_name":"long intergenic non-protein coding RNA 1571 [Source:HGNC Symbol;Acc:HGNC:51384]","synonyms":"TCONS_00024399","biotype":"lincRNA","ncbi_id":"101927364","summary":null,"start":51762519,"end":51773173,"strand":1,"description":"long intergenic non-protein coding RNA 1571 [Source:HGNC Symbol;Acc:HGNC:51384]"}, {"versioned_ensembl_gene_id":"ENSG00000182632.15","gene_symbol":"CCNYL2","gene_name":"cyclin Y-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23495]","synonyms":"CCNYL2P,C10orf21,bA178A10.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"414194","summary":null,"start":42408168,"end":42475349,"strand":-1,"description":"cyclin Y-like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23495]"}, {"versioned_ensembl_gene_id":"ENSG00000092758.15","gene_symbol":"COL9A3","gene_name":"collagen type IX alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2219]","synonyms":"IDD,FLJ90759,EDM3,DJ885L7.4.1,MED","biotype":"protein_coding","ncbi_id":"1299","summary":"This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. Mutations in this gene are associated with multiple epiphyseal dysplasia type 3. [provided by RefSeq, Jan 2010]","start":62816244,"end":62841159,"strand":1,"description":"collagen type IX alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2219]"}, {"versioned_ensembl_gene_id":"ENSG00000198754.5","gene_symbol":"OXCT2","gene_name":"3-oxoacid CoA-transferase 2 [Source:HGNC Symbol;Acc:HGNC:18606]","synonyms":"SCOT-T,FLJ00030,FKSG25","biotype":"protein_coding","ncbi_id":"64064","summary":"The protein encoded by this gene catalyzes the transfer of a CoA group from succinate to acetoacetate and is an important enzyme in ketone body catabolism. The encoded protein localizes to the mitochondrion. This gene is intronless, and a pseudogene of this gene is located elsewhere on chromosome 1. [provided by RefSeq, Aug 2016]","start":39769523,"end":39771348,"strand":-1,"description":"3-oxoacid CoA-transferase 2 [Source:HGNC Symbol;Acc:HGNC:18606]"}, {"versioned_ensembl_gene_id":"ENSG00000237641.1","gene_symbol":"AC073476.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231789481,"end":231789887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257126.5","gene_symbol":"FOXG1-AS1","gene_name":"FOXG1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50663]","synonyms":"FOXG1-AS","biotype":"antisense_RNA","ncbi_id":"103695363","summary":null,"start":28729083,"end":28765277,"strand":-1,"description":"FOXG1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50663]"}, {"versioned_ensembl_gene_id":"ENSG00000144524.17","gene_symbol":"COPS7B","gene_name":"COP9 signalosome subunit 7B [Source:HGNC Symbol;Acc:HGNC:16760]","synonyms":"CSN7B","biotype":"protein_coding","ncbi_id":"64708","summary":null,"start":231781671,"end":231809254,"strand":1,"description":"COP9 signalosome subunit 7B [Source:HGNC Symbol;Acc:HGNC:16760]"}, {"versioned_ensembl_gene_id":"ENSG00000084072.16","gene_symbol":"PPIE","gene_name":"peptidylprolyl isomerase E [Source:HGNC Symbol;Acc:HGNC:9258]","synonyms":"MGC3736,MGC111222,CyP-33","biotype":"protein_coding","ncbi_id":"10450","summary":"The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein contains a highly conserved cyclophilin (CYP) domain as well as an RNA-binding domain. It was shown to possess PPIase and protein folding activities, and it also exhibits RNA-binding activity. Alternative splicing results in multiple transcript variants. A related pseudogene, which is also located on chromosome 1, has been identified. [provided by RefSeq, Aug 2010]","start":39692182,"end":39763914,"strand":1,"description":"peptidylprolyl isomerase E [Source:HGNC Symbol;Acc:HGNC:9258]"}, {"versioned_ensembl_gene_id":"ENSG00000099956.18","gene_symbol":"SMARCB1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 [Source:HGNC Symbol;Acc:HGNC:11103]","synonyms":"PPP1R144,Ini1,Snr1,hSNFS,SNF5L1,BAF47,Sfh1p,RDT","biotype":"protein_coding","ncbi_id":"6598","summary":"The protein encoded by this gene is part of a complex that relieves repressive chromatin structures, allowing the transcriptional machinery to access its targets more effectively. The encoded nuclear protein may also bind to and enhance the DNA joining activity of HIV-1 integrase. This gene has been found to be a tumor suppressor, and mutations in it have been associated with malignant rhabdoid tumors. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":23786963,"end":23834516,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 [Source:HGNC Symbol;Acc:HGNC:11103]"}, {"versioned_ensembl_gene_id":"ENSG00000280214.1","gene_symbol":"AC027682.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":67550815,"end":67552935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276232.1","gene_symbol":"AC006064.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":6510275,"end":6510522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232114.1","gene_symbol":"AC018693.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38769265,"end":38770124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259804.1","gene_symbol":"AC027682.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67561411,"end":67562309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234856.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29464377,"end":29469587,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000237718.2","gene_symbol":"AC009095.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67614381,"end":67616146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278830.1","gene_symbol":"AL355493.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27313723,"end":27316587,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227238.1","gene_symbol":"TTC39DP","gene_name":"tetratricopeptide repeat domain 39D, pseudogene [Source:HGNC Symbol;Acc:HGNC:35451]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"646640","summary":null,"start":38763534,"end":38765221,"strand":1,"description":"tetratricopeptide repeat domain 39D, pseudogene [Source:HGNC Symbol;Acc:HGNC:35451]"}, {"versioned_ensembl_gene_id":"ENSG00000111639.7","gene_symbol":"MRPL51","gene_name":"mitochondrial ribosomal protein L51 [Source:HGNC Symbol;Acc:HGNC:14044]","synonyms":"HSPC241,CDA09,bMRP64,MRP64","biotype":"protein_coding","ncbi_id":"51258","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Pseudogenes corresponding to this gene are found on chromosomes 4p and 21q. [provided by RefSeq, Jul 2008]","start":6491886,"end":6493841,"strand":-1,"description":"mitochondrial ribosomal protein L51 [Source:HGNC Symbol;Acc:HGNC:14044]"}, {"versioned_ensembl_gene_id":"ENSG00000102974.14","gene_symbol":"CTCF","gene_name":"CCCTC-binding factor [Source:HGNC Symbol;Acc:HGNC:13723]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10664","summary":"This gene is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. This nuclear protein is able to use different combinations of the ZF domains to bind different DNA target sequences and proteins. Depending upon the context of the site, the protein can bind a histone acetyltransferase (HAT)-containing complex and function as a transcriptional activator or bind a histone deacetylase (HDAC)-containing complex and function as a transcriptional repressor. If the protein is bound to a transcriptional insulator element, it can block communication between enhancers and upstream promoters, thereby regulating imprinted expression. Mutations in this gene have been associated with invasive breast cancers, prostate cancers, and Wilms' tumors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":67562407,"end":67639183,"strand":1,"description":"CCCTC-binding factor [Source:HGNC Symbol;Acc:HGNC:13723]"}, {"versioned_ensembl_gene_id":"ENSG00000215409.4","gene_symbol":"AL355493.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27331357,"end":27341252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162825.16","gene_symbol":"NBPF20","gene_name":"NBPF member 20 [Source:HGNC Symbol;Acc:HGNC:32000]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288142","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Mar 2014]","start":145289900,"end":145405778,"strand":-1,"description":"NBPF member 20 [Source:HGNC Symbol;Acc:HGNC:32000]"}, {"versioned_ensembl_gene_id":"ENSG00000178722.12","gene_symbol":"C5orf64","gene_name":"chromosome 5 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:26744]","synonyms":"FLJ37543","biotype":"processed_transcript","ncbi_id":"285668","summary":null,"start":61637708,"end":61751763,"strand":1,"description":"chromosome 5 open reading frame 64 [Source:HGNC Symbol;Acc:HGNC:26744]"}, {"versioned_ensembl_gene_id":"ENSG00000279239.1","gene_symbol":"AL391099.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42470082,"end":42470268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243838.1","gene_symbol":"PSMC1P7","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646085","summary":null,"start":161328924,"end":161330238,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39782]"}, {"versioned_ensembl_gene_id":"ENSG00000104938.16","gene_symbol":"CLEC4M","gene_name":"C-type lectin domain family 4 member M [Source:HGNC Symbol;Acc:HGNC:13523]","synonyms":"CD209L,LSIGN,HP10347,DCSIGNR,DC-SIGNR,DC-SIGN2,CD299","biotype":"protein_coding","ncbi_id":"10332","summary":"This gene encodes a C-type lectin that functions in cell adhesion and pathogen recognition. This receptor recognizes a wide range of evolutionarily divergent pathogens with a large impact on public health, including tuberculosis mycobacteria, and viruses including Ebola, hepatitis C, HIV-1, influenza A, West Nile virus and the SARS-CoV acute respiratory syndrome coronavirus. The protein is organized into four distinct domains: a C-terminal carbohydrate recognition domain, a flexible tandem-repeat neck domain of variable length, a transmembrane region and an N-terminal cytoplasmic domain involved in internalization. This gene is closely related in terms of both sequence and function to a neighboring gene, CD209 (Gene ID: 30835), also known as DC-SIGN. The two genes differ in viral recognition and expression patterns, with this gene showing high expression in endothelial cells of the liver, lymph node and placenta. Polymorphisms in the tandem repeat neck domain are associated with resistance to SARS infection. [provided by RefSeq, May 2020]","start":7763149,"end":7769605,"strand":1,"description":"C-type lectin domain family 4 member M [Source:HGNC Symbol;Acc:HGNC:13523]"}, {"versioned_ensembl_gene_id":"ENSG00000009709.11","gene_symbol":"PAX7","gene_name":"paired box 7 [Source:HGNC Symbol;Acc:HGNC:8621]","synonyms":"Hup1","biotype":"protein_coding","ncbi_id":"5081","summary":"This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. The specific function of the paired box 7 gene is unknown but speculated to involve tumor suppression since fusion of this gene with a forkhead domain family member has been associated with alveolar rhabdomyosarcoma. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":18631006,"end":18748866,"strand":1,"description":"paired box 7 [Source:HGNC Symbol;Acc:HGNC:8621]"}, {"versioned_ensembl_gene_id":"ENSG00000181222.15","gene_symbol":"POLR2A","gene_name":"RNA polymerase II subunit A [Source:HGNC Symbol;Acc:HGNC:9187]","synonyms":"RPB1,POLRA,POLR2","biotype":"protein_coding","ncbi_id":"5430","summary":"This gene encodes the largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene contains a carboxy terminal domain composed of heptapeptide repeats that are essential for polymerase activity. These repeats contain serine and threonine residues that are phosphorylated in actively transcribing RNA polymerase. In addition, this subunit, in combination with several other polymerase subunits, forms the DNA binding domain of the polymerase, a groove in which the DNA template is transcribed into RNA. [provided by RefSeq, Jul 2008]","start":7484366,"end":7514616,"strand":1,"description":"RNA polymerase II subunit A [Source:HGNC Symbol;Acc:HGNC:9187]"}, {"versioned_ensembl_gene_id":"ENSG00000251575.2","gene_symbol":"C5orf64-AS1","gene_name":"C5orf64 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52969]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506526","summary":null,"start":61732774,"end":61735669,"strand":-1,"description":"C5orf64 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52969]"}, {"versioned_ensembl_gene_id":"ENSG00000144893.12","gene_symbol":"MED12L","gene_name":"mediator complex subunit 12 like [Source:HGNC Symbol;Acc:HGNC:16050]","synonyms":"TRALPUSH,TRALP,TNRC11L,KIAA1635","biotype":"protein_coding","ncbi_id":"116931","summary":"The protein encoded by this gene is part of the Mediator complex, which is involved in transcriptional coactivation of nearly all RNA polymerase II-dependent genes. The Mediator complex links gene-specific transcriptional activators with the basal transcription machinery. [provided by RefSeq, May 2010]","start":151085697,"end":151437072,"strand":1,"description":"mediator complex subunit 12 like [Source:HGNC Symbol;Acc:HGNC:16050]"}, {"versioned_ensembl_gene_id":"ENSG00000234943.2","gene_symbol":"AC092839.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54545368,"end":54546677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213516.9","gene_symbol":"RBMXL1","gene_name":"RNA binding motif protein, X-linked like 1 [Source:HGNC Symbol;Acc:HGNC:25073]","synonyms":"KAT3","biotype":"protein_coding","ncbi_id":"494115","summary":"This gene represents a retrogene of RNA binding motif protein, X-linked (RBMX), which is located on chromosome X. While all introns in the coding sequence have been processed out compared to the RBMX locus, the ORF is intact and there is specific evidence for transcription at this location. The preservation of the ORF by purifying selection in all Old World monkeys carrying it suggests that this locus is likely to be functional, possibly during male meiosis when X chromosomal genes are silenced or during haploid stages of spermatogenesis. This gene shares 5' exon structure with the cysteine conjugate-beta lyase 2 locus on chromosome 1, but the coding sequences are non-overlapping. Alternative splicing results in two transcript variants. [provided by RefSeq, Jun 2009]","start":88979456,"end":88992960,"strand":-1,"description":"RNA binding motif protein, X-linked like 1 [Source:HGNC Symbol;Acc:HGNC:25073]"}, {"versioned_ensembl_gene_id":"ENSG00000160948.13","gene_symbol":"VPS28","gene_name":"VPS28, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:18178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51160","summary":"This gene encodes a protein subunit of the ESCRT-I complex (endosomal complexes required for transport), which functions in the transport and sorting of proteins into subcellular vesicles. This complex can also be hijacked to facilitate the budding of enveloped viruses from the cell membrane. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":144423601,"end":144428563,"strand":-1,"description":"VPS28, ESCRT-I subunit [Source:HGNC Symbol;Acc:HGNC:18178]"}, {"versioned_ensembl_gene_id":"ENSG00000248529.5","gene_symbol":"AC026746.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61658474,"end":61698432,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164136.16","gene_symbol":"IL15","gene_name":"interleukin 15 [Source:HGNC Symbol;Acc:HGNC:5977]","synonyms":"MGC9721,IL-15","biotype":"protein_coding","ncbi_id":"3600","summary":"The protein encoded by this gene is a cytokine that regulates T and natural killer cell activation and proliferation. This cytokine and interleukine 2 share many biological activities. They are found to bind common hematopoietin receptor subunits, and may compete for the same receptor, and thus negatively regulate each other's activity. The number of CD8+ memory cells is shown to be controlled by a balance between this cytokine and IL2. This cytokine induces the activation of JAK kinases, as well as the phosphorylation and activation of transcription activators STAT3, STAT5, and STAT6. Studies of the mouse counterpart suggested that this cytokine may increase the expression of apoptosis inhibitor BCL2L1/BCL-x(L), possibly through the transcription activation activity of STAT6, and thus prevent apoptosis. Alternatively spliced transcript variants of this gene have been reported. [provided by RefSeq, Feb 2011]","start":141636599,"end":141733987,"strand":1,"description":"interleukin 15 [Source:HGNC Symbol;Acc:HGNC:5977]"}, {"versioned_ensembl_gene_id":"ENSG00000225727.2","gene_symbol":"AL139184.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":44437207,"end":44452827,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249878.1","gene_symbol":"AC026434.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61831947,"end":61833024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280357.1","gene_symbol":"AL138960.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":44432144,"end":44432678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248199.1","gene_symbol":"AC026434.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61878109,"end":61886129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253429.1","gene_symbol":"AP005660.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94708952,"end":94709244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129055.12","gene_symbol":"ANAPC13","gene_name":"anaphase promoting complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:24540]","synonyms":"SWM1,DKFZP566D193,APC13","biotype":"protein_coding","ncbi_id":"25847","summary":"This gene encodes a component of the anaphase promoting complex, a large ubiquitin-protein ligase that controls cell cycle progression by regulating the degradation of cell cycle regulators such as B-type cyclins. The encoded protein is evolutionarily conserved and is required for the integrity and ubiquitin ligase activity of the anaphase promoting complex. Pseudogenes and splice variants have been found for this gene; however, the biological validity of some of the splice variants has not been determined. [provided by RefSeq, Nov 2008]","start":134477706,"end":134486716,"strand":-1,"description":"anaphase promoting complex subunit 13 [Source:HGNC Symbol;Acc:HGNC:24540]"}, {"versioned_ensembl_gene_id":"ENSG00000272877.1","gene_symbol":"DDX11L8","gene_name":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100302090","summary":null,"start":12310,"end":13501,"strand":1,"description":"DEAD/H-box helicase 11 like 8 [Source:HGNC Symbol;Acc:HGNC:37101]"}, {"versioned_ensembl_gene_id":"ENSG00000088298.12","gene_symbol":"EDEM2","gene_name":"ER degradation enhancing alpha-mannosidase like protein 2 [Source:HGNC Symbol;Acc:HGNC:15877]","synonyms":"FLJ10783,C20orf49,C20orf31,bA4204.1","biotype":"protein_coding","ncbi_id":"55741","summary":"In the endoplasmic reticulum (ER), misfolded proteins are retrotranslocated to the cytosol and degraded by the proteasome in a process known as ER-associated degradation (ERAD). EDEM2 belongs to a family of proteins involved in ERAD of glycoproteins (Mast et al., 2005 [PubMed 15537790]).[supplied by OMIM, Mar 2008]","start":35115357,"end":35147364,"strand":-1,"description":"ER degradation enhancing alpha-mannosidase like protein 2 [Source:HGNC Symbol;Acc:HGNC:15877]"}, {"versioned_ensembl_gene_id":"ENSG00000278016.2","gene_symbol":"TIGD5","gene_name":"tigger transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:18336]","synonyms":"FLJ14926","biotype":"protein_coding","ncbi_id":"84948","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":143597835,"end":143603224,"strand":1,"description":"tigger transposable element derived 5 [Source:HGNC Symbol;Acc:HGNC:18336]"}, {"versioned_ensembl_gene_id":"ENSG00000276686.1","gene_symbol":"KIR2DL5A","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]","synonyms":"KIR2DL5,CD158F,KIR2DL5.1,CD158F,KIR2DL5.1,KIR2DL5","biotype":"protein_coding","ncbi_id":"57292","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832558,"end":54842109,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A [Source:HGNC Symbol;Acc:HGNC:16345]"}, {"versioned_ensembl_gene_id":"ENSG00000239911.2","gene_symbol":"PRKAG2-AS1","gene_name":"PRKAG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40468]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505483","summary":null,"start":151877042,"end":151879223,"strand":1,"description":"PRKAG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40468]"}, {"versioned_ensembl_gene_id":"ENSG00000228350.1","gene_symbol":"CELSR3-AS1","gene_name":"CELSR3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50302]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102724368","summary":null,"start":48663776,"end":48669174,"strand":1,"description":"CELSR3 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:50302]"}, {"versioned_ensembl_gene_id":"ENSG00000223476.1","gene_symbol":"VN1R42P","gene_name":"vomeronasal 1 receptor 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:37362]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312794","summary":null,"start":64933273,"end":64933616,"strand":1,"description":"vomeronasal 1 receptor 42 pseudogene [Source:HGNC Symbol;Acc:HGNC:37362]"}, {"versioned_ensembl_gene_id":"ENSG00000271973.1","gene_symbol":"AC141002.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48672455,"end":48672733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278201.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54802913,"end":54813989,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000260773.1","gene_symbol":"AC055855.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66314914,"end":66331703,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166938.12","gene_symbol":"DIS3L","gene_name":"DIS3 like exosome 3'-5' exoribonuclease [Source:HGNC Symbol;Acc:HGNC:28698]","synonyms":"KIAA1955,FLJ38088,DIS3L1,MGC4562","biotype":"protein_coding","ncbi_id":"115752","summary":"The cytoplasmic RNA exosome complex degrades unstable mRNAs and is involved in the regular turnover of other mRNAs. The protein encoded by this gene contains 3'-5' exoribonuclease activity and is a catalytic component of this complex. [provided by RefSeq, May 2016]","start":66293217,"end":66333898,"strand":1,"description":"DIS3 like exosome 3'-5' exoribonuclease [Source:HGNC Symbol;Acc:HGNC:28698]"}, {"versioned_ensembl_gene_id":"ENSG00000175662.17","gene_symbol":"TOM1L2","gene_name":"target of myb1 like 2 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11984]","synonyms":null,"biotype":"protein_coding","ncbi_id":"146691","summary":"This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Apr 2017]","start":17843511,"end":17972422,"strand":-1,"description":"target of myb1 like 2 membrane trafficking protein [Source:HGNC Symbol;Acc:HGNC:11984]"}, {"versioned_ensembl_gene_id":"ENSG00000261386.2","gene_symbol":"AC027682.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":67549214,"end":67563958,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184166.2","gene_symbol":"OR1D2","gene_name":"olfactory receptor family 1 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8183]","synonyms":"OR17-4,OLFR1","biotype":"protein_coding","ncbi_id":"4991","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3088484,"end":3104422,"strand":-1,"description":"olfactory receptor family 1 subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:8183]"}, {"versioned_ensembl_gene_id":"ENSG00000160951.3","gene_symbol":"PTGER1","gene_name":"prostaglandin E receptor 1 [Source:HGNC Symbol;Acc:HGNC:9593]","synonyms":"EP1","biotype":"protein_coding","ncbi_id":"5731","summary":"The protein encoded by this gene is a member of the G protein-coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). Through a phosphatidylinositol-calcium second messenger system, G-Q proteins mediate this receptor's activity. Knockout studies in mice suggested a role of this receptor in mediating algesia and in regulation of blood pressure. Studies in mice also suggested that this gene may mediate adrenocorticotropic hormone response to bacterial endotoxin. [provided by RefSeq, Jul 2008]","start":14472466,"end":14475362,"strand":-1,"description":"prostaglandin E receptor 1 [Source:HGNC Symbol;Acc:HGNC:9593]"}, {"versioned_ensembl_gene_id":"ENSG00000235044.1","gene_symbol":"PPIAP3","gene_name":"peptidylprolyl isomerase A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16545]","synonyms":"bA425M5.2","biotype":"processed_pseudogene","ncbi_id":"170539","summary":null,"start":37530039,"end":37530543,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16545]"}, {"versioned_ensembl_gene_id":"ENSG00000174944.8","gene_symbol":"P2RY14","gene_name":"purinergic receptor P2Y14 [Source:HGNC Symbol;Acc:HGNC:16442]","synonyms":"KIAA0001,GPR105","biotype":"protein_coding","ncbi_id":"9934","summary":"The product of this gene belongs to the family of G-protein coupled receptors, which contains several receptor subtypes with different pharmacological selectivity for various adenosine and uridine nucleotides. This receptor is a P2Y purinergic receptor for UDP-glucose and other UDP-sugars coupled to G-proteins. It has been implicated in extending the known immune system functions of P2Y receptors by participating in the regulation of the stem cell compartment, and it may also play a role in neuroimmune function. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]","start":151212117,"end":151278467,"strand":-1,"description":"purinergic receptor P2Y14 [Source:HGNC Symbol;Acc:HGNC:16442]"}, {"versioned_ensembl_gene_id":"ENSG00000142163.8","gene_symbol":"OR1E3","gene_name":"olfactory receptor family 1 subfamily E member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8191]","synonyms":"OR1E3P,OR17-210","biotype":"unprocessed_pseudogene","ncbi_id":"8389","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3116427,"end":3117374,"strand":1,"description":"olfactory receptor family 1 subfamily E member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8191]"}, {"versioned_ensembl_gene_id":"ENSG00000270948.1","gene_symbol":"MTDHP1","gene_name":"metadherin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418814","summary":null,"start":64942143,"end":64942926,"strand":-1,"description":"metadherin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52357]"}, {"versioned_ensembl_gene_id":"ENSG00000280424.1","gene_symbol":"BX537318.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46006616,"end":46010777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240255.1","gene_symbol":"PSMC1P6","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643766","summary":null,"start":87630301,"end":87631619,"strand":-1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39781]"}, {"versioned_ensembl_gene_id":"ENSG00000183024.3","gene_symbol":"OR1G1","gene_name":"olfactory receptor family 1 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:8204]","synonyms":"OR1G2,OR17-209","biotype":"protein_coding","ncbi_id":"8390","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3126584,"end":3127581,"strand":-1,"description":"olfactory receptor family 1 subfamily G member 1 [Source:HGNC Symbol;Acc:HGNC:8204]"}, {"versioned_ensembl_gene_id":"ENSG00000260638.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"C6orf101,HLA-90,dJ377H14.3","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797597,"end":29799601,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000276114.2","gene_symbol":"CCL23","gene_name":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]","synonyms":"SCYA23,MPIF-1,MIP-3,CKb8,Ckb-8","biotype":"protein_coding","ncbi_id":"6368","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, displays chemotactic activity on resting T lymphocytes and monocytes, lower activity on neutrophils and no activity on activated T lymphocytes. The protein is also a strong suppressor of colony formation by a multipotential hematopoietic progenitor cell line. In addition, the product of this gene is a potent agonist of the chemokine (C-C motif) receptor 1. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":36013092,"end":36018001,"strand":-1,"description":"C-C motif chemokine ligand 23 [Source:HGNC Symbol;Acc:HGNC:10622]"}, {"versioned_ensembl_gene_id":"ENSG00000233113.4","gene_symbol":"AL844851.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800376,"end":29801172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257164.5","gene_symbol":"LINC02451","gene_name":"long intergenic non-protein coding RNA 2451 [Source:HGNC Symbol;Acc:HGNC:53383]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369738","summary":null,"start":42646583,"end":42686701,"strand":1,"description":"long intergenic non-protein coding RNA 2451 [Source:HGNC Symbol;Acc:HGNC:53383]"}, {"versioned_ensembl_gene_id":"ENSG00000274469.1","gene_symbol":"LINC01746","gene_name":"long intergenic non-protein coding RNA 1746 [Source:HGNC Symbol;Acc:HGNC:52534]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372608","summary":null,"start":37571103,"end":37583935,"strand":1,"description":"long intergenic non-protein coding RNA 1746 [Source:HGNC Symbol;Acc:HGNC:52534]"}, {"versioned_ensembl_gene_id":"ENSG00000179914.4","gene_symbol":"ITLN1","gene_name":"intelectin 1 [Source:HGNC Symbol;Acc:HGNC:18259]","synonyms":"LFR,ITLN,HL-1,hIntL,FLJ20022","biotype":"protein_coding","ncbi_id":"55600","summary":null,"start":160876539,"end":160885170,"strand":-1,"description":"intelectin 1 [Source:HGNC Symbol;Acc:HGNC:18259]"}, {"versioned_ensembl_gene_id":"ENSG00000240759.1","gene_symbol":"RPS27P21","gene_name":"ribosomal protein S27 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35826]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131905","summary":null,"start":42678873,"end":42679124,"strand":-1,"description":"ribosomal protein S27 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35826]"}, {"versioned_ensembl_gene_id":"ENSG00000224355.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29809741,"end":29809872,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000179046.8","gene_symbol":"TRIML2","gene_name":"tripartite motif family like 2 [Source:HGNC Symbol;Acc:HGNC:26378]","synonyms":"SPRYD6,FLJ25801","biotype":"protein_coding","ncbi_id":"205860","summary":"This gene encodes a member of the tri-partite motif (TRIM) family of proteins. This protein may be regulated by the tumor suppressor p53 and may regulate p53 through the enhancement of p53 SUMOylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":188091273,"end":188109603,"strand":-1,"description":"tripartite motif family like 2 [Source:HGNC Symbol;Acc:HGNC:26378]"}, {"versioned_ensembl_gene_id":"ENSG00000099958.14","gene_symbol":"DERL3","gene_name":"derlin 3 [Source:HGNC Symbol;Acc:HGNC:14236]","synonyms":"C22orf14,MGC71803,IZP6,FLJ43842,derlin-3","biotype":"protein_coding","ncbi_id":"91319","summary":"The protein encoded by this gene belongs to the derlin family, and resides in the endoplasmic reticulum (ER). Proteins that are unfolded or misfolded in the ER must be refolded or degraded to maintain the homeostasis of the ER. This protein appears to be involved in the degradation of misfolded glycoproteins in the ER. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008]","start":23834503,"end":23839128,"strand":-1,"description":"derlin 3 [Source:HGNC Symbol;Acc:HGNC:14236]"}, {"versioned_ensembl_gene_id":"ENSG00000228234.1","gene_symbol":"GLRXP1","gene_name":"glutaredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16544]","synonyms":"bA425M5.1,GLRXP","biotype":"processed_pseudogene","ncbi_id":"170522","summary":null,"start":37602852,"end":37603185,"strand":-1,"description":"glutaredoxin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16544]"}, {"versioned_ensembl_gene_id":"ENSG00000225759.1","gene_symbol":"LINC00489","gene_name":"long intergenic non-protein coding RNA 489 [Source:HGNC Symbol;Acc:HGNC:43426]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861522","summary":null,"start":37619298,"end":37623119,"strand":-1,"description":"long intergenic non-protein coding RNA 489 [Source:HGNC Symbol;Acc:HGNC:43426]"}, {"versioned_ensembl_gene_id":"ENSG00000138271.5","gene_symbol":"GPR87","gene_name":"G protein-coupled receptor 87 [Source:HGNC Symbol;Acc:HGNC:4538]","synonyms":"GPR95","biotype":"protein_coding","ncbi_id":"53836","summary":"This gene encodes a G protein-coupled receptor and is located in a cluster of G protein-couple receptor genes on chromosome 3. The encoded protein has been shown to be overexpressed in lung squamous cell carcinoma (PMID:18057535) and regulated by p53 (PMID:19602589). [provided by RefSeq, Nov 2011]","start":151294086,"end":151316952,"strand":-1,"description":"G protein-coupled receptor 87 [Source:HGNC Symbol;Acc:HGNC:4538]"}, {"versioned_ensembl_gene_id":"ENSG00000204117.1","gene_symbol":"AL162293.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37676910,"end":37683234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144597.13","gene_symbol":"EAF1","gene_name":"ELL associated factor 1 [Source:HGNC Symbol;Acc:HGNC:20907]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85403","summary":null,"start":15427355,"end":15450635,"strand":1,"description":"ELL associated factor 1 [Source:HGNC Symbol;Acc:HGNC:20907]"}, {"versioned_ensembl_gene_id":"ENSG00000231479.8","gene_symbol":"SLC44A4","gene_name":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]","synonyms":"C6orf29,FLJ14491,TPPT,CTL4,NG22","biotype":"protein_coding","ncbi_id":"80736","summary":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":31850729,"end":31866590,"strand":-1,"description":"solute carrier family 44 member 4 [Source:HGNC Symbol;Acc:HGNC:13941]"}, {"versioned_ensembl_gene_id":"ENSG00000173947.13","gene_symbol":"PIFO","gene_name":"primary cilia formation [Source:HGNC Symbol;Acc:HGNC:27009]","synonyms":"pitchfork,FLJ23853,C1orf88","biotype":"protein_coding","ncbi_id":"128344","summary":null,"start":111346288,"end":111353013,"strand":1,"description":"primary cilia formation [Source:HGNC Symbol;Acc:HGNC:27009]"}, {"versioned_ensembl_gene_id":"ENSG00000234032.9","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a,VARS2L","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30986796,"end":31005022,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000242048.3","gene_symbol":"AC093583.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":151806490,"end":151810820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106617.13","gene_symbol":"PRKAG2","gene_name":"protein kinase AMP-activated non-catalytic subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:9386]","synonyms":"AAKG,WPWS,H91620p,CMH6,AAKG2","biotype":"protein_coding","ncbi_id":"51422","summary":"AMP-activated protein kinase (AMPK) is a heterotrimeric protein composed of a catalytic alpha subunit, a noncatalytic beta subunit, and a noncatalytic regulatory gamma subunit. Various forms of each of these subunits exist, encoded by different genes. AMPK is an important energy-sensing enzyme that monitors cellular energy status and functions by inactivating key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This gene is a member of the AMPK gamma subunit family. Mutations in this gene have been associated with Wolff-Parkinson-White syndrome, familial hypertrophic cardiomyopathy, and glycogen storage disease of the heart. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jan 2015]","start":151556111,"end":151877125,"strand":-1,"description":"protein kinase AMP-activated non-catalytic subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:9386]"}, {"versioned_ensembl_gene_id":"ENSG00000198910.12","gene_symbol":"L1CAM","gene_name":"L1 cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:6470]","synonyms":"CD171,SPG1,S10,MIC5,MASA,HSAS1,HSAS","biotype":"protein_coding","ncbi_id":"3897","summary":"The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of this gene results in multiple transcript variants, some of which include an alternate exon that is considered to be specific to neurons. [provided by RefSeq, May 2013]","start":153861514,"end":153909223,"strand":-1,"description":"L1 cell adhesion molecule [Source:HGNC Symbol;Acc:HGNC:6470]"}, {"versioned_ensembl_gene_id":"ENSG00000253399.1","gene_symbol":"AC078852.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1358479,"end":1359461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163945.16","gene_symbol":"UVSSA","gene_name":"UV stimulated scaffold protein A [Source:HGNC Symbol;Acc:HGNC:29304]","synonyms":"KIAA1530","biotype":"protein_coding","ncbi_id":"57654","summary":"The protein encoded by this gene appears to be involved in ubiquitination and dephosphorylation of RNA polymerase II subunits that stall after UV irradiation. The encoded protein interacts with several members of the nucleotide excision repair complex, and is thought to be involved in the transcription-coupled nucleotide excision repair (TC-NER) pathway to help remove lesions in the DNA that block transcription. Defects in this gene can cause UV-sensitive syndrome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":1347266,"end":1395992,"strand":1,"description":"UV stimulated scaffold protein A [Source:HGNC Symbol;Acc:HGNC:29304]"}, {"versioned_ensembl_gene_id":"ENSG00000272555.1","gene_symbol":"AC009974.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":218818690,"end":218819144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255275.3","gene_symbol":"AL080251.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18849273,"end":18921121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236393.1","gene_symbol":"AC091806.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40262917,"end":40287720,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214045.3","gene_symbol":"AC091807.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40359183,"end":40360726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235685.2","gene_symbol":"AC092473.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40514895,"end":40515508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179002.5","gene_symbol":"TAS1R2","gene_name":"taste 1 receptor member 2 [Source:HGNC Symbol;Acc:HGNC:14905]","synonyms":"TR2,T1R2,GPR71","biotype":"protein_coding","ncbi_id":"80834","summary":null,"start":18839599,"end":18859682,"strand":-1,"description":"taste 1 receptor member 2 [Source:HGNC Symbol;Acc:HGNC:14905]"}, {"versioned_ensembl_gene_id":"ENSG00000198246.7","gene_symbol":"SLC29A3","gene_name":"solute carrier family 29 member 3 [Source:HGNC Symbol;Acc:HGNC:23096]","synonyms":"FLJ11160,ENT3","biotype":"protein_coding","ncbi_id":"55315","summary":"This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]","start":71319258,"end":71363385,"strand":1,"description":"solute carrier family 29 member 3 [Source:HGNC Symbol;Acc:HGNC:23096]"}, {"versioned_ensembl_gene_id":"ENSG00000224543.4","gene_symbol":"SNRPGP15","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49371]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130932","summary":null,"start":14489388,"end":14489609,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49371]"}, {"versioned_ensembl_gene_id":"ENSG00000010292.12","gene_symbol":"NCAPD2","gene_name":"non-SMC condensin I complex subunit D2 [Source:HGNC Symbol;Acc:HGNC:24305]","synonyms":"KIAA0159,hCAP-D2,CNAP1,CAP-D2","biotype":"protein_coding","ncbi_id":"9918","summary":null,"start":6493356,"end":6531955,"strand":1,"description":"non-SMC condensin I complex subunit D2 [Source:HGNC Symbol;Acc:HGNC:24305]"}, {"versioned_ensembl_gene_id":"ENSG00000123159.15","gene_symbol":"GIPC1","gene_name":"GIPC PDZ domain containing family member 1 [Source:HGNC Symbol;Acc:HGNC:1226]","synonyms":"TIP-2,SYNECTIN,SEMCAP,RGS19IP1,NIP,Hs.6454,GLUT1CBP,GIPC,C19orf3","biotype":"protein_coding","ncbi_id":"10755","summary":"GIPC1 is a scaffolding protein that regulates cell surface receptor expression and trafficking (Lee et al., 2008 [PubMed 18775991]).[supplied by OMIM, Apr 2009]","start":14477760,"end":14496149,"strand":-1,"description":"GIPC PDZ domain containing family member 1 [Source:HGNC Symbol;Acc:HGNC:1226]"}, {"versioned_ensembl_gene_id":"ENSG00000251569.1","gene_symbol":"AC093899.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":169479480,"end":169525922,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169991.10","gene_symbol":"IFFO2","gene_name":"intermediate filament family orphan 2 [Source:HGNC Symbol;Acc:HGNC:27006]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126917","summary":null,"start":18904281,"end":18956686,"strand":-1,"description":"intermediate filament family orphan 2 [Source:HGNC Symbol;Acc:HGNC:27006]"}, {"versioned_ensembl_gene_id":"ENSG00000241011.1","gene_symbol":"AC108073.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188106558,"end":188106914,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196542.8","gene_symbol":"SPTSSB","gene_name":"serine palmitoyltransferase small subunit B [Source:HGNC Symbol;Acc:HGNC:24045]","synonyms":"ssSPTb,C3orf57,ADMP","biotype":"protein_coding","ncbi_id":"165679","summary":"Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTB is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010]","start":161344792,"end":161372880,"strand":-1,"description":"serine palmitoyltransferase small subunit B [Source:HGNC Symbol;Acc:HGNC:24045]"}, {"versioned_ensembl_gene_id":"ENSG00000239474.6","gene_symbol":"KLHL41","gene_name":"kelch like family member 41 [Source:HGNC Symbol;Acc:HGNC:16905]","synonyms":"SARCOSIN,Krp1,KBTBD10","biotype":"protein_coding","ncbi_id":"10324","summary":"This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]","start":169509702,"end":169526262,"strand":1,"description":"kelch like family member 41 [Source:HGNC Symbol;Acc:HGNC:16905]"}, {"versioned_ensembl_gene_id":"ENSG00000198483.12","gene_symbol":"ANKRD35","gene_name":"ankyrin repeat domain 35 [Source:HGNC Symbol;Acc:HGNC:26323]","synonyms":"FLJ25124","biotype":"protein_coding","ncbi_id":"148741","summary":null,"start":145866560,"end":145885866,"strand":-1,"description":"ankyrin repeat domain 35 [Source:HGNC Symbol;Acc:HGNC:26323]"}, {"versioned_ensembl_gene_id":"ENSG00000213754.2","gene_symbol":"AL356317.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64305047,"end":64306733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137970.7","gene_symbol":"RPL7P9","gene_name":"ribosomal protein L7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653702","summary":null,"start":96678874,"end":96679620,"strand":-1,"description":"ribosomal protein L7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37028]"}, {"versioned_ensembl_gene_id":"ENSG00000262085.2","gene_symbol":"OR1P1","gene_name":"olfactory receptor family 1 subfamily P member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8222]","synonyms":"OR1P1P,OR17-208","biotype":"polymorphic_pseudogene","ncbi_id":"8391","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":3153889,"end":3154882,"strand":-1,"description":"olfactory receptor family 1 subfamily P member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8222]"}, {"versioned_ensembl_gene_id":"ENSG00000105671.11","gene_symbol":"DDX49","gene_name":"DEAD-box helicase 49 [Source:HGNC Symbol;Acc:HGNC:18684]","synonyms":"Dbp8,FLJ10432","biotype":"protein_coding","ncbi_id":"54555","summary":null,"start":18919675,"end":18928633,"strand":1,"description":"DEAD-box helicase 49 [Source:HGNC Symbol;Acc:HGNC:18684]"}, {"versioned_ensembl_gene_id":"ENSG00000261848.5","gene_symbol":"AC090282.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3134969,"end":3177031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189030.9","gene_symbol":"VHLL","gene_name":"VHL like [Source:HGNC Symbol;Acc:HGNC:30666]","synonyms":"VLP,VHLP","biotype":"protein_coding","ncbi_id":"391104","summary":"Von Hippel-Lindau (VHL) tumor suppressor protein is a component of an E3 ubiquitin ligase complex that selectively ubiquitinates the alpha subunit of the hypoxia-inducible factor (HIF) transcription factor for proteasome-mediated degradation. Inactivation of VHL causes VHL disease and sporadic kidney cancer. This gene encodes a VHL homolog that lacks one of two key domains necessary for VHL function. This gene may contribute to the regulation of oxygen homeostasis and neovascularization during placenta development. This gene is intronless, and can also be interpreted as a retrotransposed pseudogene of the VHL locus located on chromosome 3. However, the protein is represented in this RefSeq due to evidence in PMID:14757845 that strongly suggests it is translated. The same publication also indicates that this protein binds HIF alpha but fails to recruit the E3 ubiquitin ligase complex, and it therefore functions as a dominant-negative VHL protein and a protector of HIF alpha. [provided by RefSeq, Jan 2010]","start":156298624,"end":156299299,"strand":-1,"description":"VHL like [Source:HGNC Symbol;Acc:HGNC:30666]"}, {"versioned_ensembl_gene_id":"ENSG00000223621.1","gene_symbol":"AK4P4","gene_name":"adenylate kinase 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39067]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128705","summary":null,"start":5855781,"end":5856426,"strand":-1,"description":"adenylate kinase 4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39067]"}, {"versioned_ensembl_gene_id":"ENSG00000249142.1","gene_symbol":"AC074134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32522758,"end":32523865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280802.1","gene_symbol":"ITPK1-AS1","gene_name":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]","synonyms":"NCRNA00203,ITPK1AS,ITPK1-AS,C14orf85","biotype":"antisense_RNA","ncbi_id":"319085","summary":null,"start":93067452,"end":93072152,"strand":1,"description":"ITPK1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:20132]"}, {"versioned_ensembl_gene_id":"ENSG00000172150.4","gene_symbol":"OR1A2","gene_name":"olfactory receptor family 1 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8180]","synonyms":"OR17-6","biotype":"protein_coding","ncbi_id":"26189","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3197519,"end":3198448,"strand":1,"description":"olfactory receptor family 1 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8180]"}, {"versioned_ensembl_gene_id":"ENSG00000269888.1","gene_symbol":"AC112491.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161429112,"end":161429613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240567.1","gene_symbol":"LINC02067","gene_name":"long intergenic non-protein coding RNA 2067 [Source:HGNC Symbol;Acc:HGNC:52913]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101243545","summary":null,"start":161426427,"end":161448242,"strand":1,"description":"long intergenic non-protein coding RNA 2067 [Source:HGNC Symbol;Acc:HGNC:52913]"}, {"versioned_ensembl_gene_id":"ENSG00000262911.5","gene_symbol":"DNAJC28","gene_name":"DnaJ heat shock protein family (Hsp40) member C28 [Source:HGNC Symbol;Acc:HGNC:1297]","synonyms":"C21orf78,C21orf55","biotype":"protein_coding","ncbi_id":"54943","summary":"This gene encodes a member of the DnaJ heat shock protein family. The encoded protein, which contains a conserved N-terminal DnaJ domain, is thought to play a role in protein folding or act as a molecular chaperone protein. [provided by RefSeq, Oct 2016]","start":33495087,"end":33501278,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C28 [Source:HGNC Symbol;Acc:HGNC:1297]"}, {"versioned_ensembl_gene_id":"ENSG00000274669.5","gene_symbol":"LILRB1","gene_name":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]","synonyms":"PIRB,CD85,LIR-1,PIR-B,ILT2,MIR-7,CD85j,LIR1","biotype":"protein_coding","ncbi_id":"10859","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54548949,"end":54569575,"strand":1,"description":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]"}, {"versioned_ensembl_gene_id":"ENSG00000275361.1","gene_symbol":"AC245517.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22087924,"end":22088085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232668.1","gene_symbol":"AC010967.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52883243,"end":52883455,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280939.1","gene_symbol":"AC134684.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7592980,"end":7593243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228312.1","gene_symbol":"GAPDHP45","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:37802]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240710","summary":null,"start":15093263,"end":15093611,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:37802]"}, {"versioned_ensembl_gene_id":"ENSG00000204544.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]","synonyms":"C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2,C6orf205","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":30983718,"end":30989903,"strand":1,"description":"mucin 21, cell surface associated [Source:HGNC Symbol;Acc:HGNC:21661]"}, {"versioned_ensembl_gene_id":"ENSG00000244464.1","gene_symbol":"AC107029.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99598064,"end":99623820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078900.14","gene_symbol":"TP73","gene_name":"tumor protein p73 [Source:HGNC Symbol;Acc:HGNC:12003]","synonyms":"P73","biotype":"protein_coding","ncbi_id":"7161","summary":"This gene encodes a member of the p53 family of transcription factors involved in cellular responses to stress and development. It maps to a region on chromosome 1p36 that is frequently deleted in neuroblastoma and other tumors, and thought to contain multiple tumor suppressor genes. The demonstration that this gene is monoallelically expressed (likely from the maternal allele), supports the notion that it is a candidate gene for neuroblastoma. Many transcript variants resulting from alternative splicing and/or use of alternate promoters have been found for this gene, but the biological validity and the full-length nature of some variants have not been determined. [provided by RefSeq, Feb 2011]","start":3652520,"end":3736201,"strand":1,"description":"tumor protein p73 [Source:HGNC Symbol;Acc:HGNC:12003]"}, {"versioned_ensembl_gene_id":"ENSG00000100897.17","gene_symbol":"DCAF11","gene_name":"DDB1 and CUL4 associated factor 11 [Source:HGNC Symbol;Acc:HGNC:20258]","synonyms":"WDR23,PRO2389,GL014","biotype":"protein_coding","ncbi_id":"80344","summary":"This gene encodes a WD repeat-containing protein that interacts with the COP9 signalosome, a macromolecular complex that interacts with cullin-RING E3 ligases and regulates their activity by hydrolyzing cullin-Nedd8 conjugates. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2009]","start":24114195,"end":24125242,"strand":1,"description":"DDB1 and CUL4 associated factor 11 [Source:HGNC Symbol;Acc:HGNC:20258]"}, {"versioned_ensembl_gene_id":"ENSG00000142684.8","gene_symbol":"ZNF593","gene_name":"zinc finger protein 593 [Source:HGNC Symbol;Acc:HGNC:30943]","synonyms":"ZT86","biotype":"protein_coding","ncbi_id":"51042","summary":null,"start":26169871,"end":26170873,"strand":1,"description":"zinc finger protein 593 [Source:HGNC Symbol;Acc:HGNC:30943]"}, {"versioned_ensembl_gene_id":"ENSG00000130173.13","gene_symbol":"ANGPTL8","gene_name":"angiopoietin like 8 [Source:HGNC Symbol;Acc:HGNC:24933]","synonyms":"TD26,RIFL,C19orf80","biotype":"protein_coding","ncbi_id":"55908","summary":null,"start":11237450,"end":11241943,"strand":1,"description":"angiopoietin like 8 [Source:HGNC Symbol;Acc:HGNC:24933]"}, {"versioned_ensembl_gene_id":"ENSG00000229001.1","gene_symbol":"ACTBP14","gene_name":"actin, beta pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:45086]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389976","summary":null,"start":69022778,"end":69023866,"strand":1,"description":"actin, beta pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:45086]"}, {"versioned_ensembl_gene_id":"ENSG00000223744.1","gene_symbol":"RBMY2GP","gene_name":"RNA binding motif protein, Y-linked, family 2, member G pseudogene [Source:HGNC Symbol;Acc:HGNC:23892]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"378952","summary":null,"start":6328052,"end":6343323,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member G pseudogene [Source:HGNC Symbol;Acc:HGNC:23892]"}, {"versioned_ensembl_gene_id":"ENSG00000229341.2","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"TNXBS,XBS,TNXB1,XB,TNXB2","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32140675,"end":32153125,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000227098.1","gene_symbol":"AC073636.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176845993,"end":176849428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279205.1","gene_symbol":"AC092162.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":176822030,"end":176823653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224748.4","gene_symbol":"TAP1","gene_name":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]","synonyms":"D6S114E,RING4,ABCB2,PSF1","biotype":"protein_coding","ncbi_id":"6890","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]","start":32935926,"end":32944695,"strand":-1,"description":"transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]"}, {"versioned_ensembl_gene_id":"ENSG00000269635.1","gene_symbol":"AC004257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15221015,"end":15222297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000066855.15","gene_symbol":"MTFR1","gene_name":"mitochondrial fission regulator 1 [Source:HGNC Symbol;Acc:HGNC:29510]","synonyms":"KIAA0009,FAM54A2,CHPPR","biotype":"protein_coding","ncbi_id":"9650","summary":"This gene encodes a mitochondrial protein that is characterized by a poly-proline rich region. A chicken homolog of this protein promotes mitochondrial fission and the mouse homolog protects cells from oxidative stress. A related pseudogene of this gene is found on chromosome X. [provided by RefSeq, Mar 2009]","start":65644734,"end":65771261,"strand":1,"description":"mitochondrial fission regulator 1 [Source:HGNC Symbol;Acc:HGNC:29510]"}, {"versioned_ensembl_gene_id":"ENSG00000129535.12","gene_symbol":"NRL","gene_name":"neural retina leucine zipper [Source:HGNC Symbol;Acc:HGNC:8002]","synonyms":"RP27,NRL-MAF,D14S46E","biotype":"protein_coding","ncbi_id":"4901","summary":"This gene encodes a basic motif-leucine zipper transcription factor of the Maf subfamily. The encoded protein is conserved among vertebrates and is a critical intrinsic regulator of photoceptor development and function. Mutations in this gene have been associated with retinitis pigmentosa and retinal degenerative diseases. [provided by RefSeq, Jul 2008]","start":24080107,"end":24115014,"strand":-1,"description":"neural retina leucine zipper [Source:HGNC Symbol;Acc:HGNC:8002]"}, {"versioned_ensembl_gene_id":"ENSG00000101447.14","gene_symbol":"FAM83D","gene_name":"family with sequence similarity 83 member D [Source:HGNC Symbol;Acc:HGNC:16122]","synonyms":"dJ616B8.3,CHICA,C20orf129","biotype":"protein_coding","ncbi_id":"81610","summary":null,"start":38926312,"end":38953106,"strand":1,"description":"family with sequence similarity 83 member D [Source:HGNC Symbol;Acc:HGNC:16122]"}, {"versioned_ensembl_gene_id":"ENSG00000277130.1","gene_symbol":"AC073569.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":79818784,"end":79819465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258048.1","gene_symbol":"AC073569.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79690144,"end":79778451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258044.1","gene_symbol":"AC073569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":79823778,"end":79825496,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255398.2","gene_symbol":"HCAR3","gene_name":"hydroxycarboxylic acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:16824]","synonyms":"HM74,HCA3,GPR109B","biotype":"protein_coding","ncbi_id":"8843","summary":null,"start":122714756,"end":122716892,"strand":-1,"description":"hydroxycarboxylic acid receptor 3 [Source:HGNC Symbol;Acc:HGNC:16824]"}, {"versioned_ensembl_gene_id":"ENSG00000279844.1","gene_symbol":"AC096656.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":160849313,"end":160850676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270733.1","gene_symbol":"AL355877.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26263041,"end":26263398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174720.15","gene_symbol":"LARP7","gene_name":"La ribonucleoprotein domain family member 7 [Source:HGNC Symbol;Acc:HGNC:24912]","synonyms":"PIP7S,HDCMA18P,DKFZP564K112","biotype":"protein_coding","ncbi_id":"51574","summary":"This gene encodes a protein which is found in the 7SK snRNP (small nuclear ribonucleoprotein). This snRNP complex inhibits a cyclin-dependent kinase, positive transcription elongation factor b, which is required for paused RNA polymerase II at a promoter to begin transcription elongation. A pseudogene of this gene is located on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]","start":112636964,"end":112657592,"strand":1,"description":"La ribonucleoprotein domain family member 7 [Source:HGNC Symbol;Acc:HGNC:24912]"}, {"versioned_ensembl_gene_id":"ENSG00000250869.2","gene_symbol":"AC087359.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":67133554,"end":67135911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151876.12","gene_symbol":"FBXO4","gene_name":"F-box protein 4 [Source:HGNC Symbol;Acc:HGNC:13583]","synonyms":"FBX4","biotype":"protein_coding","ncbi_id":"26272","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":41925254,"end":41941743,"strand":1,"description":"F-box protein 4 [Source:HGNC Symbol;Acc:HGNC:13583]"}, {"versioned_ensembl_gene_id":"ENSG00000265496.5","gene_symbol":"AC100778.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49487339,"end":49491878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227351.2","gene_symbol":"NANOGP6","gene_name":"Nanog homeobox pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23104]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"414134","summary":null,"start":99788564,"end":99789410,"strand":-1,"description":"Nanog homeobox pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:23104]"}, {"versioned_ensembl_gene_id":"ENSG00000196208.13","gene_symbol":"GREB1","gene_name":"growth regulation by estrogen in breast cancer 1 [Source:HGNC Symbol;Acc:HGNC:24885]","synonyms":"KIAA0575","biotype":"protein_coding","ncbi_id":"9687","summary":"This gene is an estrogen-responsive gene that is an early response gene in the estrogen receptor-regulated pathway. It is thought to play an important role in hormone-responsive tissues and cancer. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":11482341,"end":11642788,"strand":1,"description":"growth regulation by estrogen in breast cancer 1 [Source:HGNC Symbol;Acc:HGNC:24885]"}, {"versioned_ensembl_gene_id":"ENSG00000112365.4","gene_symbol":"ZBTB24","gene_name":"zinc finger and BTB domain containing 24 [Source:HGNC Symbol;Acc:HGNC:21143]","synonyms":"ZNF450,PATZ2,KIAA0441,BIF1","biotype":"protein_coding","ncbi_id":"9841","summary":"This gene encodes a protein similar to a protein in rodents which is induced by bone morphogenic protein 2 in vitro. [provided by RefSeq, Aug 2011]","start":109462594,"end":109483237,"strand":-1,"description":"zinc finger and BTB domain containing 24 [Source:HGNC Symbol;Acc:HGNC:21143]"}, {"versioned_ensembl_gene_id":"ENSG00000131899.10","gene_symbol":"LLGL1","gene_name":"LLGL1, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6628]","synonyms":"Mgl1,LLGL,Lgl1,HUGL-1,HUGL,DLG4","biotype":"protein_coding","ncbi_id":"3996","summary":"This gene encodes a protein that is similar to a tumor suppressor in Drosophila. The protein is part of a cytoskeletal network and is associated with nonmuscle myosin II heavy chain and a kinase that specifically phosphorylates this protein at serine residues. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":18225587,"end":18244875,"strand":1,"description":"LLGL1, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6628]"}, {"versioned_ensembl_gene_id":"ENSG00000160216.18","gene_symbol":"AGPAT3","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:326]","synonyms":"LPAAT-gamma","biotype":"protein_coding","ncbi_id":"56894","summary":"The protein encoded by this gene is an acyltransferase that converts lysophosphatidic acid into phosphatidic acid, which is the second step in the de novo phospholipid biosynthetic pathway. The encoded protein may be an integral membrane protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":43865186,"end":43986536,"strand":1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:326]"}, {"versioned_ensembl_gene_id":"ENSG00000273598.1","gene_symbol":"AC211486.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75316048,"end":75327765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232860.7","gene_symbol":"SMG7-AS1","gene_name":"SMG7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24518]","synonyms":"DKFZP564C196","biotype":"processed_transcript","ncbi_id":"284649","summary":null,"start":183460874,"end":183472265,"strand":-1,"description":"SMG7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24518]"}, {"versioned_ensembl_gene_id":"ENSG00000231646.5","gene_symbol":"FSIP2-AS1","gene_name":"FSIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40978]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"107985781","summary":null,"start":185783691,"end":185800151,"strand":-1,"description":"FSIP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40978]"}, {"versioned_ensembl_gene_id":"ENSG00000276160.1","gene_symbol":"GGTLC5P","gene_name":"gamma-glutamyltransferase light chain 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:33427]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"653590","summary":null,"start":18340145,"end":18345899,"strand":1,"description":"gamma-glutamyltransferase light chain 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:33427]"}, {"versioned_ensembl_gene_id":"ENSG00000196975.15","gene_symbol":"ANXA4","gene_name":"annexin A4 [Source:HGNC Symbol;Acc:HGNC:542]","synonyms":"ANX4","biotype":"protein_coding","ncbi_id":"307","summary":"Annexin IV (ANX4) belongs to the annexin family of calcium-dependent phospholipid binding proteins. Although their functions are still not clearly defined, several members of the annexin family have been implicated in membrane-related events along exocytotic and endocytotic pathways. ANX4 has 45 to 59% identity with other members of its family and shares a similar size and exon-intron organization. Isolated from human placenta, ANX4 encodes a protein that has possible interactions with ATP, and has in vitro anticoagulant activity and also inhibits phospholipase A2 activity. ANX4 is almost exclusively expressed in epithelial cells. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2016]","start":69644425,"end":69827100,"strand":1,"description":"annexin A4 [Source:HGNC Symbol;Acc:HGNC:542]"}, {"versioned_ensembl_gene_id":"ENSG00000111666.10","gene_symbol":"CHPT1","gene_name":"choline phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:17852]","synonyms":"CPT1","biotype":"protein_coding","ncbi_id":"56994","summary":null,"start":101696947,"end":101744140,"strand":1,"description":"choline phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:17852]"}, {"versioned_ensembl_gene_id":"ENSG00000235523.1","gene_symbol":"AL135924.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72257336,"end":72257783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270699.1","gene_symbol":"AC012493.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100377421,"end":100377532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254858.9","gene_symbol":"MPV17L2","gene_name":"MPV17 mitochondrial inner membrane protein like 2 [Source:HGNC Symbol;Acc:HGNC:28177]","synonyms":"MGC12972,FKSG24","biotype":"protein_coding","ncbi_id":"84769","summary":null,"start":18193182,"end":18196948,"strand":1,"description":"MPV17 mitochondrial inner membrane protein like 2 [Source:HGNC Symbol;Acc:HGNC:28177]"}, {"versioned_ensembl_gene_id":"ENSG00000263388.1","gene_symbol":"AC002347.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10680734,"end":10683988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231551.8","gene_symbol":"AC245100.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":148402516,"end":148432545,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147256.11","gene_symbol":"ARHGAP36","gene_name":"Rho GTPase activating protein 36 [Source:HGNC Symbol;Acc:HGNC:26388]","synonyms":"FLJ30058","biotype":"protein_coding","ncbi_id":"158763","summary":null,"start":131058242,"end":131089883,"strand":1,"description":"Rho GTPase activating protein 36 [Source:HGNC Symbol;Acc:HGNC:26388]"}, {"versioned_ensembl_gene_id":"ENSG00000164327.12","gene_symbol":"RICTOR","gene_name":"RPTOR independent companion of MTOR complex 2 [Source:HGNC Symbol;Acc:HGNC:28611]","synonyms":"PIA,MGC39830,KIAA1999,AVO3","biotype":"protein_coding","ncbi_id":"253260","summary":"RICTOR and MTOR (FRAP1; MIM 601231) are components of a protein complex that integrates nutrient- and growth factor-derived signals to regulate cell growth (Sarbassov et al., 2004 [PubMed 15268862]).[supplied by OMIM, Mar 2008]","start":38937919,"end":39074408,"strand":-1,"description":"RPTOR independent companion of MTOR complex 2 [Source:HGNC Symbol;Acc:HGNC:28611]"}, {"versioned_ensembl_gene_id":"ENSG00000235711.4","gene_symbol":"ANKRD34C","gene_name":"ankyrin repeat domain 34C [Source:HGNC Symbol;Acc:HGNC:33888]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390616","summary":null,"start":79293285,"end":79298235,"strand":1,"description":"ankyrin repeat domain 34C [Source:HGNC Symbol;Acc:HGNC:33888]"}, {"versioned_ensembl_gene_id":"ENSG00000257221.3","gene_symbol":"AC007569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108628687,"end":108641318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282779.1","gene_symbol":"AC243660.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28529259,"end":28529484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282479.1","gene_symbol":"ABCB10P3","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31129]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728248","summary":null,"start":28515677,"end":28517839,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31129]"}, {"versioned_ensembl_gene_id":"ENSG00000239572.1","gene_symbol":"AC117513.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87731402,"end":87793629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272563.1","gene_symbol":"AC016745.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113432600,"end":113436042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234422.1","gene_symbol":"UBE2WP1","gene_name":"ubiquitin conjugating enzyme E2 W pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32198]","synonyms":"UBE2WP","biotype":"processed_pseudogene","ncbi_id":"619457","summary":null,"start":96418594,"end":96418933,"strand":1,"description":"ubiquitin conjugating enzyme E2 W pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32198]"}, {"versioned_ensembl_gene_id":"ENSG00000274540.2","gene_symbol":"PRR23D1","gene_name":"proline rich 23 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:49420]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131608","summary":null,"start":7531604,"end":7534426,"strand":1,"description":"proline rich 23 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:49420]"}, {"versioned_ensembl_gene_id":"ENSG00000227579.5","gene_symbol":"AL122019.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177393287,"end":177597709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237894.5","gene_symbol":"HCG22","gene_name":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]","synonyms":"FLJ37114,PBMUCL2","biotype":"processed_transcript","ncbi_id":"285834","summary":null,"start":31098991,"end":31104790,"strand":1,"description":"HLA complex group 22 [Source:HGNC Symbol;Acc:HGNC:27780]"}, {"versioned_ensembl_gene_id":"ENSG00000232709.1","gene_symbol":"MARK2P9","gene_name":"microtubule affinity regulating kinase 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39800]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507674","summary":null,"start":92418667,"end":92420875,"strand":1,"description":"microtubule affinity regulating kinase 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39800]"}, {"versioned_ensembl_gene_id":"ENSG00000182287.14","gene_symbol":"AP1S2","gene_name":"adaptor related protein complex 1 sigma 2 subunit [Source:HGNC Symbol;Acc:HGNC:560]","synonyms":"MRXS5,MRX59,SIGMA1B,PGS","biotype":"protein_coding","ncbi_id":"8905","summary":"Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as the small subunit of this complex and is a member of the adaptin protein family. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013]","start":15825806,"end":15854931,"strand":-1,"description":"adaptor related protein complex 1 sigma 2 subunit [Source:HGNC Symbol;Acc:HGNC:560]"}, {"versioned_ensembl_gene_id":"ENSG00000243252.1","gene_symbol":"AL731683.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32582946,"end":32585541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206237.6","gene_symbol":"HLA-DQB1","gene_name":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]","synonyms":"HLA-DQB,CELIAC1,IDDM1","biotype":"protein_coding","ncbi_id":"3119","summary":"HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]","start":32582490,"end":32590101,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 1 [Source:HGNC Symbol;Acc:HGNC:4944]"}, {"versioned_ensembl_gene_id":"ENSG00000152670.18","gene_symbol":"DDX4","gene_name":"DEAD-box helicase 4 [Source:HGNC Symbol;Acc:HGNC:18700]","synonyms":"VASA","biotype":"protein_coding","ncbi_id":"54514","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a homolog of VASA proteins in Drosophila and several other species. The gene is specifically expressed in the germ cell lineage in both sexes and functions in germ cell development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":55738017,"end":55817157,"strand":1,"description":"DEAD-box helicase 4 [Source:HGNC Symbol;Acc:HGNC:18700]"}, {"versioned_ensembl_gene_id":"ENSG00000102032.12","gene_symbol":"RENBP","gene_name":"renin binding protein [Source:HGNC Symbol;Acc:HGNC:9959]","synonyms":"RNBP,RBP","biotype":"protein_coding","ncbi_id":"5973","summary":"The gene product inhibits renin activity by forming a dimer with renin, a complex known as high molecular weight renin. The encoded protein contains a leucine zipper domain, which is essential for its dimerization with renin. The gene product can catalyze the interconversion of N-acetylglucosamine to N-acetylmannosamine, indicating that it is a GlcNAc 2-epimerase. Transcript variants utilizing alternative promoters have been described in the literature. [provided by RefSeq, Jul 2008]","start":153935263,"end":153944691,"strand":-1,"description":"renin binding protein [Source:HGNC Symbol;Acc:HGNC:9959]"}, {"versioned_ensembl_gene_id":"ENSG00000213509.4","gene_symbol":"PPIAP16","gene_name":"peptidylprolyl isomerase A pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:9269]","synonyms":"PPIP6","biotype":"processed_pseudogene","ncbi_id":"5488","summary":null,"start":57941818,"end":57942304,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:9269]"}, {"versioned_ensembl_gene_id":"ENSG00000249209.2","gene_symbol":"AP000311.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":33584687,"end":33931607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237039.1","gene_symbol":"AC018738.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231256097,"end":231256306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273102.1","gene_symbol":"AP000569.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33967101,"end":33968573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229047.1","gene_symbol":"AF127577.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14961309,"end":14964233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279390.1","gene_symbol":"AF127577.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":15050189,"end":15052379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105173.13","gene_symbol":"CCNE1","gene_name":"cyclin E1 [Source:HGNC Symbol;Acc:HGNC:1589]","synonyms":"CCNE","biotype":"protein_coding","ncbi_id":"898","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK2, whose activity is required for cell cycle G1/S transition. This protein accumulates at the G1-S phase boundary and is degraded as cells progress through S phase. Overexpression of this gene has been observed in many tumors, which results in chromosome instability, and thus may contribute to tumorigenesis. This protein was found to associate with, and be involved in, the phosphorylation of NPAT protein (nuclear protein mapped to the ATM locus), which participates in cell-cycle regulated histone gene expression and plays a critical role in promoting cell-cycle progression in the absence of pRB. [provided by RefSeq, Apr 2016]","start":29811898,"end":29824308,"strand":1,"description":"cyclin E1 [Source:HGNC Symbol;Acc:HGNC:1589]"}, {"versioned_ensembl_gene_id":"ENSG00000279678.1","gene_symbol":"AC090386.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":37305295,"end":37306333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180530.10","gene_symbol":"NRIP1","gene_name":"nuclear receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8001]","synonyms":"RIP140","biotype":"protein_coding","ncbi_id":"8204","summary":"Nuclear receptor interacting protein 1 (NRIP1) is a nuclear protein that specifically interacts with the hormone-dependent activation domain AF2 of nuclear receptors. Also known as RIP140, this protein modulates transcriptional activity of the estrogen receptor. [provided by RefSeq, Jul 2008]","start":14961235,"end":15065936,"strand":-1,"description":"nuclear receptor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:8001]"}, {"versioned_ensembl_gene_id":"ENSG00000259513.1","gene_symbol":"CYCSP38","gene_name":"cytochrome c, somatic pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:24411]","synonyms":"HCP38,HC2","biotype":"transcribed_processed_pseudogene","ncbi_id":"360184","summary":null,"start":60558080,"end":60558401,"strand":1,"description":"cytochrome c, somatic pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:24411]"}, {"versioned_ensembl_gene_id":"ENSG00000259481.1","gene_symbol":"AC012404.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61181249,"end":61195938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277006.2","gene_symbol":"DEFB104B","gene_name":"defensin beta 104B [Source:HGNC Symbol;Acc:HGNC:26165]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503618","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 104, DEFB104A and DEFB104B, in head-to-head orientation. This gene, DEFB104B, represents the more telomeric copy. [provided by RefSeq, Oct 2014]","start":7462290,"end":7467065,"strand":-1,"description":"defensin beta 104B [Source:HGNC Symbol;Acc:HGNC:26165]"}, {"versioned_ensembl_gene_id":"ENSG00000283481.1","gene_symbol":"MTND4LP32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52318]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"109729156","summary":null,"start":57169143,"end":57169412,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:52318]"}, {"versioned_ensembl_gene_id":"ENSG00000227122.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32224781,"end":32230795,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000231537.1","gene_symbol":"MTCO3P10","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:52040]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075152","summary":null,"start":57167880,"end":57168651,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:52040]"}, {"versioned_ensembl_gene_id":"ENSG00000127314.17","gene_symbol":"RAP1B","gene_name":"RAP1B, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9857]","synonyms":"RAL1B,K-REV,DKFZp586H0723","biotype":"protein_coding","ncbi_id":"5908","summary":"This gene encodes a member of the RAS-like small GTP-binding protein superfamily. Members of this family regulate multiple cellular processes including cell adhesion and growth and differentiation. This protein localizes to cellular membranes and has been shown to regulate integrin-mediated cell signaling. This protein also plays a role in regulating outside-in signaling in platelets. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 5, 6 and 9. [provided by RefSeq, Oct 2011]","start":68610839,"end":68671901,"strand":1,"description":"RAP1B, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9857]"}, {"versioned_ensembl_gene_id":"ENSG00000127990.15","gene_symbol":"SGCE","gene_name":"sarcoglycan epsilon [Source:HGNC Symbol;Acc:HGNC:10808]","synonyms":"DYT11","biotype":"protein_coding","ncbi_id":"8910","summary":"This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2. [provided by RefSeq, Oct 2016]","start":94585230,"end":94656209,"strand":-1,"description":"sarcoglycan epsilon [Source:HGNC Symbol;Acc:HGNC:10808]"}, {"versioned_ensembl_gene_id":"ENSG00000164967.9","gene_symbol":"RPP25L","gene_name":"ribonuclease P/MRP subunit p25 like [Source:HGNC Symbol;Acc:HGNC:19909]","synonyms":"MGC29635,C9orf23,bA296L22.5","biotype":"protein_coding","ncbi_id":"138716","summary":"This gene encodes a protein that appears to belong to a family of evolutionarily related proteins (DUF78), that may share one or more domains in common. Members of this family are small archaebacterial proteins with no known function. Alternative splicing has been observed at this locus and two variants, both encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":34610486,"end":34612104,"strand":-1,"description":"ribonuclease P/MRP subunit p25 like [Source:HGNC Symbol;Acc:HGNC:19909]"}, {"versioned_ensembl_gene_id":"ENSG00000243733.1","gene_symbol":"AC018450.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143111802,"end":143112359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267371.1","gene_symbol":"AP001017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11552366,"end":11552847,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233542.1","gene_symbol":"AL391845.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2013213,"end":2015530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267127.7","gene_symbol":"AC090360.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":80034346,"end":80097088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227629.1","gene_symbol":"SLC25A15P1","gene_name":"solute carrier family 25 member 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18497]","synonyms":"SLC25A15PY1,SLC25A15P","biotype":"unprocessed_pseudogene","ncbi_id":"100422624","summary":null,"start":26586642,"end":26591601,"strand":-1,"description":"solute carrier family 25 member 15 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18497]"}, {"versioned_ensembl_gene_id":"ENSG00000281154.1","gene_symbol":"AC019173.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68587305,"end":68595199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237926.1","gene_symbol":"AC239367.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51162864,"end":51163677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116117.17","gene_symbol":"PARD3B","gene_name":"par-3 family cell polarity regulator beta [Source:HGNC Symbol;Acc:HGNC:14446]","synonyms":"Par3L,PAR3beta,ALS2CR19","biotype":"protein_coding","ncbi_id":"117583","summary":null,"start":204545793,"end":205620162,"strand":1,"description":"par-3 family cell polarity regulator beta [Source:HGNC Symbol;Acc:HGNC:14446]"}, {"versioned_ensembl_gene_id":"ENSG00000159625.14","gene_symbol":"DRC7","gene_name":"dynein regulatory complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:25289]","synonyms":"FAP50,DKFZp434I099,CFAP50,CCDC135,C16orf50","biotype":"protein_coding","ncbi_id":"84229","summary":null,"start":57694793,"end":57731805,"strand":1,"description":"dynein regulatory complex subunit 7 [Source:HGNC Symbol;Acc:HGNC:25289]"}, {"versioned_ensembl_gene_id":"ENSG00000137441.7","gene_symbol":"FGFBP2","gene_name":"fibroblast growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29451]","synonyms":"KSP37","biotype":"protein_coding","ncbi_id":"83888","summary":"This gene encodes a member of the fibroblast growth factor binding protein family. The encoded protein is a serum protein that is selectively secreted by cytotoxic lymphocytes and may be involved in cytotoxic lymphocyte-mediated immunity. An increase in the amount of gene product may be associated with atopic asthma and mild extrinsic asthma.[provided by RefSeq Staff, Oct 2008]","start":15960243,"end":15969309,"strand":-1,"description":"fibroblast growth factor binding protein 2 [Source:HGNC Symbol;Acc:HGNC:29451]"}, {"versioned_ensembl_gene_id":"ENSG00000146555.18","gene_symbol":"SDK1","gene_name":"sidekick cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:19307]","synonyms":"FLJ31425","biotype":"protein_coding","ncbi_id":"221935","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains six immunoglobulin-like domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":3301448,"end":4269000,"strand":1,"description":"sidekick cell adhesion molecule 1 [Source:HGNC Symbol;Acc:HGNC:19307]"}, {"versioned_ensembl_gene_id":"ENSG00000137055.14","gene_symbol":"PLAA","gene_name":"phospholipase A2 activating protein [Source:HGNC Symbol;Acc:HGNC:9043]","synonyms":"DOA1,PLAP,PLA2P,FLJ12699,FLJ11281","biotype":"protein_coding","ncbi_id":"9373","summary":null,"start":26904083,"end":26947463,"strand":-1,"description":"phospholipase A2 activating protein [Source:HGNC Symbol;Acc:HGNC:9043]"}, {"versioned_ensembl_gene_id":"ENSG00000224593.1","gene_symbol":"AC092427.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":3337889,"end":3338601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188050.2","gene_symbol":"RNF133","gene_name":"ring finger protein 133 [Source:HGNC Symbol;Acc:HGNC:21154]","synonyms":null,"biotype":"protein_coding","ncbi_id":"168433","summary":"The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene has no intron. [provided by RefSeq, Jul 2008]","start":122697712,"end":122699156,"strand":-1,"description":"ring finger protein 133 [Source:HGNC Symbol;Acc:HGNC:21154]"}, {"versioned_ensembl_gene_id":"ENSG00000133226.16","gene_symbol":"SRRM1","gene_name":"serine and arginine repetitive matrix 1 [Source:HGNC Symbol;Acc:HGNC:16638]","synonyms":"SRM160,POP101,MGC39488","biotype":"protein_coding","ncbi_id":"10250","summary":null,"start":24631716,"end":24673267,"strand":1,"description":"serine and arginine repetitive matrix 1 [Source:HGNC Symbol;Acc:HGNC:16638]"}, {"versioned_ensembl_gene_id":"ENSG00000073331.17","gene_symbol":"ALPK1","gene_name":"alpha kinase 1 [Source:HGNC Symbol;Acc:HGNC:20917]","synonyms":"Lak,KIAA1527,FLJ22670","biotype":"protein_coding","ncbi_id":"80216","summary":"This gene encodes an alpha kinase. Mice which were homozygous for disrupted copies of this gene exhibited coordination defects (PMID: 21208416). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":112285509,"end":112442620,"strand":1,"description":"alpha kinase 1 [Source:HGNC Symbol;Acc:HGNC:20917]"}, {"versioned_ensembl_gene_id":"ENSG00000147896.3","gene_symbol":"IFNK","gene_name":"interferon kappa [Source:HGNC Symbol;Acc:HGNC:21714]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56832","summary":"This gene encodes a member of the type I interferon family. Type I interferons are a group of related glycoproteins that play an important role in host defenses against viral infections. This protein is expressed in keratinocytes and the gene is found on chromosome 9, adjacent to the type I interferon cluster. [provided by RefSeq, Jul 2008]","start":27524314,"end":27526498,"strand":1,"description":"interferon kappa [Source:HGNC Symbol;Acc:HGNC:21714]"}, {"versioned_ensembl_gene_id":"ENSG00000274242.1","gene_symbol":"AL354976.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25244061,"end":25244854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279082.3","gene_symbol":"LINC01727","gene_name":"long intergenic non-protein coding RNA 1727 [Source:HGNC Symbol;Acc:HGNC:52515]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929625","summary":null,"start":21569976,"end":21619674,"strand":1,"description":"long intergenic non-protein coding RNA 1727 [Source:HGNC Symbol;Acc:HGNC:52515]"}, {"versioned_ensembl_gene_id":"ENSG00000185177.12","gene_symbol":"ZNF479","gene_name":"zinc finger protein 479 [Source:HGNC Symbol;Acc:HGNC:23258]","synonyms":"KR19","biotype":"protein_coding","ncbi_id":"90827","summary":null,"start":57119614,"end":57139864,"strand":-1,"description":"zinc finger protein 479 [Source:HGNC Symbol;Acc:HGNC:23258]"}, {"versioned_ensembl_gene_id":"ENSG00000276802.2","gene_symbol":"HERC2","gene_name":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]","synonyms":"p528,jdf2,D15F37S1","biotype":"protein_coding","ncbi_id":"8924","summary":"This gene belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16. [provided by RefSeq, Mar 2012]","start":28110217,"end":28435080,"strand":-1,"description":"HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]"}, {"versioned_ensembl_gene_id":"ENSG00000216938.3","gene_symbol":"RPL7P58","gene_name":"ribosomal protein L7 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:49214]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646346","summary":null,"start":26686026,"end":26687955,"strand":1,"description":"ribosomal protein L7 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:49214]"}, {"versioned_ensembl_gene_id":"ENSG00000259849.1","gene_symbol":"VENTXP1","gene_name":"VENT homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30900]","synonyms":"NA88A,CT18","biotype":"lincRNA","ncbi_id":"139538","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":26558337,"end":26561052,"strand":1,"description":"VENT homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30900]"}, {"versioned_ensembl_gene_id":"ENSG00000006530.15","gene_symbol":"AGK","gene_name":"acylglycerol kinase [Source:HGNC Symbol;Acc:HGNC:21869]","synonyms":"MULK,FLJ10842","biotype":"protein_coding","ncbi_id":"55750","summary":"The protein encoded by this gene is a mitochondrial membrane protein involved in lipid and glycerolipid metabolism. The encoded protein is a lipid kinase that catalyzes the formation of phosphatidic and lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10. [provided by RefSeq, Feb 2012]","start":141551189,"end":141655244,"strand":1,"description":"acylglycerol kinase [Source:HGNC Symbol;Acc:HGNC:21869]"}, {"versioned_ensembl_gene_id":"ENSG00000066056.13","gene_symbol":"TIE1","gene_name":"tyrosine kinase with immunoglobulin like and EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:11809]","synonyms":"TIE,JTK14","biotype":"protein_coding","ncbi_id":"7075","summary":"This gene encodes a member of the tyrosine protein kinase family. The encoded protein plays a critical role in angiogenesis and blood vessel stability by inhibiting angiopoietin 1 signaling through the endothelial receptor tyrosine kinase Tie2. Ectodomain cleavage of the encoded protein relieves inhibition of Tie2 and is mediated by multiple factors including vascular endothelial growth factor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":43300993,"end":43323108,"strand":1,"description":"tyrosine kinase with immunoglobulin like and EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:11809]"}, {"versioned_ensembl_gene_id":"ENSG00000204020.5","gene_symbol":"LIPN","gene_name":"lipase family member N [Source:HGNC Symbol;Acc:HGNC:23452]","synonyms":"LIPL4,bA186O14.3","biotype":"protein_coding","ncbi_id":"643418","summary":"The gene encodes a lipase that is highly expressed in granular keratinocytes in the epidermis, and plays a role in the differentiation of keratinocytes. Mutations in this gene are associated with lamellar ichthyosis type 4. [provided by RefSeq, Dec 2011]","start":88761406,"end":88778242,"strand":1,"description":"lipase family member N [Source:HGNC Symbol;Acc:HGNC:23452]"}, {"versioned_ensembl_gene_id":"ENSG00000279332.1","gene_symbol":"AC090772.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24135468,"end":24135829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280677.1","gene_symbol":"FAM66B","gene_name":"family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100128890","summary":null,"start":7318568,"end":7348494,"strand":-1,"description":"family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]"}, {"versioned_ensembl_gene_id":"ENSG00000083720.12","gene_symbol":"OXCT1","gene_name":"3-oxoacid CoA-transferase 1 [Source:HGNC Symbol;Acc:HGNC:8527]","synonyms":"SCOT,OXCT","biotype":"protein_coding","ncbi_id":"5019","summary":"This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency. [provided by RefSeq, Jul 2008]","start":41730065,"end":41870519,"strand":-1,"description":"3-oxoacid CoA-transferase 1 [Source:HGNC Symbol;Acc:HGNC:8527]"}, {"versioned_ensembl_gene_id":"ENSG00000255226.1","gene_symbol":"AC044839.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45750823,"end":45751871,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260281.5","gene_symbol":"ITFG1-AS1","gene_name":"ITFG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51383]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927102","summary":null,"start":47144323,"end":47162747,"strand":1,"description":"ITFG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51383]"}, {"versioned_ensembl_gene_id":"ENSG00000117859.18","gene_symbol":"OSBPL9","gene_name":"oxysterol binding protein like 9 [Source:HGNC Symbol;Acc:HGNC:16386]","synonyms":null,"biotype":"protein_coding","ncbi_id":"114883","summary":"This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain, although some members contain only the sterol-binding domain. This family member functions as a cholesterol transfer protein that regulates Golgi structure and function. Multiple transcript variants, most of which encode distinct isoforms, have been identified. Related pseudogenes have been identified on chromosomes 3, 11 and 12. [provided by RefSeq, Jul 2010]","start":51577179,"end":51798427,"strand":1,"description":"oxysterol binding protein like 9 [Source:HGNC Symbol;Acc:HGNC:16386]"}, {"versioned_ensembl_gene_id":"ENSG00000259454.1","gene_symbol":"WBP1LP5","gene_name":"WW domain binding protein 1-like pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43957]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480780","summary":null,"start":101887354,"end":101887767,"strand":-1,"description":"WW domain binding protein 1-like pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:43957]"}, {"versioned_ensembl_gene_id":"ENSG00000224372.1","gene_symbol":"HLA-N","gene_name":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]","synonyms":"HLA-30","biotype":"unprocessed_pseudogene","ncbi_id":"267014","summary":null,"start":30351416,"end":30351550,"strand":1,"description":"major histocompatibility complex, class I, N (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19406]"}, {"versioned_ensembl_gene_id":"ENSG00000238290.1","gene_symbol":"AL034417.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8026738,"end":8122702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236936.1","gene_symbol":"AL031005.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21266082,"end":21267251,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230573.1","gene_symbol":"AL513303.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3833950,"end":3834728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262246.5","gene_symbol":"CORO7","gene_name":"coronin 7 [Source:HGNC Symbol;Acc:HGNC:26161]","synonyms":"FLJ22021","biotype":"protein_coding","ncbi_id":"79585","summary":"This gene encodes a member of the coronin protein family. However, unlike other coronin proteins, it is not an actin-binding protein but rather functions as an F-actin regulator directing anterograde Golgi to endosome transport. The encoded protein has two tandem WD-40 domain repeats and localizes to the trans-Golgi network. The protein undergoes K33-linked polyubiquitination via an E3 ligase complex. It is thought to play an essential role in maintenance of Golgi apparatus morphology. Alternative splicing results in multiple transcripts variants; some of which form read-through transcripts with a neighboring gene. [provided by RefSeq, Dec 2016]","start":4354542,"end":4425705,"strand":-1,"description":"coronin 7 [Source:HGNC Symbol;Acc:HGNC:26161]"}, {"versioned_ensembl_gene_id":"ENSG00000237227.1","gene_symbol":"AL162739.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62208136,"end":62208442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274120.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000122008.15","gene_symbol":"POLK","gene_name":"DNA polymerase kappa [Source:HGNC Symbol;Acc:HGNC:9183]","synonyms":"POLQ,DINP,DINB1","biotype":"protein_coding","ncbi_id":"51426","summary":"This gene encodes a member of the DNA polymerase type-Y family of proteins. The encoded protein is a specialized DNA polymerase that catalyzes translesion DNA synthesis, which allows DNA replication in the presence of DNA lesions. Human cell lines lacking a functional copy of this gene exhibit impaired genome integrity and enhanced susceptibility to oxidative damage. Mutations in this gene that impair enzyme activity may be associated with prostate cancer in human patients. [provided by RefSeq, Sep 2016]","start":75511756,"end":75601144,"strand":1,"description":"DNA polymerase kappa [Source:HGNC Symbol;Acc:HGNC:9183]"}, {"versioned_ensembl_gene_id":"ENSG00000254651.1","gene_symbol":"AC018716.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45399448,"end":45400528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213434.2","gene_symbol":"VTI1BP2","gene_name":"vesicle transport through interaction with t-SNAREs 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43728]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389246","summary":null,"start":183483490,"end":183484185,"strand":1,"description":"vesicle transport through interaction with t-SNAREs 1B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43728]"}, {"versioned_ensembl_gene_id":"ENSG00000226501.2","gene_symbol":"USF1P1","gene_name":"upstream transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23773]","synonyms":"USF1P","biotype":"processed_pseudogene","ncbi_id":"100151645","summary":null,"start":33334571,"end":33335096,"strand":1,"description":"upstream transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23773]"}, {"versioned_ensembl_gene_id":"ENSG00000235120.1","gene_symbol":"BSN-AS1","gene_name":"BSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40102]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106478963","summary":null,"start":49640483,"end":49641769,"strand":-1,"description":"BSN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40102]"}, {"versioned_ensembl_gene_id":"ENSG00000254427.1","gene_symbol":"AC103736.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45355371,"end":45366121,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142082.14","gene_symbol":"SIRT3","gene_name":"sirtuin 3 [Source:HGNC Symbol;Acc:HGNC:14931]","synonyms":"SIR2L3","biotype":"protein_coding","ncbi_id":"23410","summary":"SIRT3 encodes a member of the sirtuin family of class III histone deacetylases, homologs to the yeast Sir2 protein. The encoded protein is found exclusively in mitochondria, where it can eliminate reactive oxygen species, inhibit apoptosis, and prevent the formation of cancer cells. SIRT3 has far-reaching effects on nuclear gene expression, cancer, cardiovascular disease, neuroprotection, aging, and metabolic control. [provided by RefSeq, May 2019]","start":215458,"end":236931,"strand":-1,"description":"sirtuin 3 [Source:HGNC Symbol;Acc:HGNC:14931]"}, {"versioned_ensembl_gene_id":"ENSG00000282641.1","gene_symbol":"AC183084.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":37996476,"end":38057692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269514.1","gene_symbol":"AC024257.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48198387,"end":48202031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265491.4","gene_symbol":"RNF115","gene_name":"ring finger protein 115 [Source:HGNC Symbol;Acc:HGNC:18154]","synonyms":"ZNF364,CL469780","biotype":"protein_coding","ncbi_id":"27246","summary":null,"start":145738868,"end":145824077,"strand":-1,"description":"ring finger protein 115 [Source:HGNC Symbol;Acc:HGNC:18154]"}, {"versioned_ensembl_gene_id":"ENSG00000155307.17","gene_symbol":"SAMSN1","gene_name":"SAM domain, SH3 domain and nuclear localization signals 1 [Source:HGNC Symbol;Acc:HGNC:10528]","synonyms":"SLy2,SH3D6B,SASH2,NASH1,HACS1","biotype":"protein_coding","ncbi_id":"64092","summary":"SAMSN1 is a member of a novel gene family of putative adaptors and scaffold proteins containing SH3 and SAM (sterile alpha motif) domains (Claudio et al., 2001 [PubMed 11536050]).[supplied by OMIM, Mar 2008]","start":14485228,"end":14583402,"strand":-1,"description":"SAM domain, SH3 domain and nuclear localization signals 1 [Source:HGNC Symbol;Acc:HGNC:10528]"}, {"versioned_ensembl_gene_id":"ENSG00000282455.1","gene_symbol":"IGHD7-27","gene_name":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]","synonyms":"IGHD727,DHQ52","biotype":"IG_D_gene","ncbi_id":"28484","summary":null,"start":105866322,"end":105866332,"strand":-1,"description":"immunoglobulin heavy diversity 7-27 [Source:HGNC Symbol;Acc:HGNC:5518]"}, {"versioned_ensembl_gene_id":"ENSG00000141425.17","gene_symbol":"RPRD1A","gene_name":"regulation of nuclear pre-mRNA domain containing 1A [Source:HGNC Symbol;Acc:HGNC:25560]","synonyms":"P15RS,HsT3101,FLJ10656","biotype":"protein_coding","ncbi_id":"55197","summary":"This gene encodes a cell-cycle and transcription regulatory protein. The encoded protein interacts with the cell cycle inhibitor cyclin-dependent kinase 4 inhibitor B and may function as a negative regulator of G(1)/S phase progression. This protein also forms homo- and hetrodimers with the protein, regulation of nuclear pre-mRNA domain-containing protein 1B, to form a scaffold that interacts with the C-terminal domain of RNA polymerase II subunit B1 and regulates several aspects of transcription. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 16. [provided by RefSeq, Dec 2014]","start":35984387,"end":36067576,"strand":-1,"description":"regulation of nuclear pre-mRNA domain containing 1A [Source:HGNC Symbol;Acc:HGNC:25560]"}, {"versioned_ensembl_gene_id":"ENSG00000232446.1","gene_symbol":"AC129850.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26147774,"end":26148281,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214111.3","gene_symbol":"AC002504.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25029545,"end":25030235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274058.3","gene_symbol":"TMPRSS11E","gene_name":"transmembrane protease, serine 11E [Source:HGNC Symbol;Acc:HGNC:24465]","synonyms":"TMPRSS11E2,DESC1","biotype":"protein_coding","ncbi_id":"28983","summary":null,"start":68447498,"end":68497649,"strand":1,"description":"transmembrane protease, serine 11E [Source:HGNC Symbol;Acc:HGNC:24465]"}, {"versioned_ensembl_gene_id":"ENSG00000244503.1","gene_symbol":"AC108751.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149494660,"end":149495995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253476.1","gene_symbol":"AC091185.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25425521,"end":25426580,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095564.13","gene_symbol":"BTAF1","gene_name":"B-TFIID TATA-box binding protein associated factor 1 [Source:HGNC Symbol;Acc:HGNC:17307]","synonyms":"TAFII170,TAF172,TAF-172,TAF(II)170,MOT1","biotype":"protein_coding","ncbi_id":"9044","summary":"This gene encodes a TAF (TATA box-binding protein-associated factor), which associates with TBP (TATA box-binding protein) to form the B-TFIID complex that is required for transcription initiation of genes by RNA polymerase II. This TAF has DNA-dependent ATPase activity, which drives the dissociation of TBP from DNA, freeing the TBP to associate with other TATA boxes or TATA-less promoters. [provided by RefSeq, Sep 2011]","start":91923769,"end":92030325,"strand":1,"description":"B-TFIID TATA-box binding protein associated factor 1 [Source:HGNC Symbol;Acc:HGNC:17307]"}, {"versioned_ensembl_gene_id":"ENSG00000260886.1","gene_symbol":"TAT-AS1","gene_name":"TAT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51369]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132529","summary":null,"start":71565789,"end":71578187,"strand":1,"description":"TAT antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51369]"}, {"versioned_ensembl_gene_id":"ENSG00000270683.1","gene_symbol":"FAM71BP1","gene_name":"family with sequence similarity 71 member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421478","summary":null,"start":25937912,"end":25938434,"strand":1,"description":"family with sequence similarity 71 member B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49805]"}, {"versioned_ensembl_gene_id":"ENSG00000234568.3","gene_symbol":"BIN2P1","gene_name":"bridging integrator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"345258","summary":null,"start":82275071,"end":82276600,"strand":1,"description":"bridging integrator 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43660]"}, {"versioned_ensembl_gene_id":"ENSG00000229421.1","gene_symbol":"AC133141.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25441164,"end":25441502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226858.7","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22,C6orf40,bA145L22.2,ZNF698","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29668984,"end":29677737,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000279344.1","gene_symbol":"AC007342.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":53478957,"end":53481550,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147082.17","gene_symbol":"CCNB3","gene_name":"cyclin B3 [Source:HGNC Symbol;Acc:HGNC:18709]","synonyms":null,"biotype":"protein_coding","ncbi_id":"85417","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as positive regulators of cyclin-dependent kinases (CDKs), and thereby play an essential role in the control of the cell cycle. Different cyclins exhibit distinct expression and degradation patterns, which contribute to the temporal coordination of each mitotic event. Studies of similar genes in chicken and drosophila suggest that this cyclin may associate with CDC2 and CDK2 kinases, and may be required for proper spindle reorganization and restoration of the interphase nucleus. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":50202713,"end":50351910,"strand":1,"description":"cyclin B3 [Source:HGNC Symbol;Acc:HGNC:18709]"}, {"versioned_ensembl_gene_id":"ENSG00000257331.1","gene_symbol":"RACGAP1P","gene_name":"Rac GTPase activating protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:24689]","synonyms":"FKSG42","biotype":"processed_pseudogene","ncbi_id":"83956","summary":null,"start":45063473,"end":45065351,"strand":-1,"description":"Rac GTPase activating protein 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:24689]"}, {"versioned_ensembl_gene_id":"ENSG00000241261.1","gene_symbol":"RPL17P19","gene_name":"ribosomal protein L17 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36919]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271150","summary":null,"start":61211652,"end":61212203,"strand":1,"description":"ribosomal protein L17 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36919]"}, {"versioned_ensembl_gene_id":"ENSG00000258491.2","gene_symbol":"AL606834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50704343,"end":50705511,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104133.14","gene_symbol":"SPG11","gene_name":"SPG11, spatacsin vesicle trafficking associated [Source:HGNC Symbol;Acc:HGNC:11226]","synonyms":"KIAA1840,FLJ21439","biotype":"protein_coding","ncbi_id":"80208","summary":"The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":44562696,"end":44663678,"strand":-1,"description":"SPG11, spatacsin vesicle trafficking associated [Source:HGNC Symbol;Acc:HGNC:11226]"}, {"versioned_ensembl_gene_id":"ENSG00000273199.1","gene_symbol":"AP000692.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36319792,"end":36320670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078674.17","gene_symbol":"PCM1","gene_name":"pericentriolar material 1 [Source:HGNC Symbol;Acc:HGNC:8727]","synonyms":"PTC4","biotype":"protein_coding","ncbi_id":"5108","summary":"The protein encoded by this gene is a component of centriolar satellites, which are electron dense granules scattered around centrosomes. Inhibition studies show that this protein is essential for the correct localization of several centrosomal proteins, and for anchoring microtubules to the centrosome. Chromosomal aberrations involving this gene are associated with papillary thyroid carcinomas and a variety of hematological malignancies, including atypical chronic myeloid leukemia and T-cell lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":17922840,"end":18029944,"strand":1,"description":"pericentriolar material 1 [Source:HGNC Symbol;Acc:HGNC:8727]"}, {"versioned_ensembl_gene_id":"ENSG00000172932.14","gene_symbol":"ANKRD13D","gene_name":"ankyrin repeat domain 13D [Source:HGNC Symbol;Acc:HGNC:27880]","synonyms":null,"biotype":"protein_coding","ncbi_id":"338692","summary":"The protein encoded by this gene is a member of the ankyrin repeat domain (ANKRD) 13 family, which currently consists of four proteins containing ubiquitin-interacting motifs. These proteins are integral membrane proteins that bind specifically to Lys-63-linked ubiquitin chains on membrane-bound proteins, targeting those proteins for rapid internalization. [provided by RefSeq, Dec 2016]","start":67288547,"end":67302485,"strand":1,"description":"ankyrin repeat domain 13D [Source:HGNC Symbol;Acc:HGNC:27880]"}, {"versioned_ensembl_gene_id":"ENSG00000131236.16","gene_symbol":"CAP1","gene_name":"cyclase associated actin cytoskeleton regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:20040]","synonyms":"CAP","biotype":"protein_coding","ncbi_id":"10487","summary":"The protein encoded by this gene is related to the S. cerevisiae CAP protein, which is involved in the cyclic AMP pathway. The human protein is able to interact with other molecules of the same protein, as well as with CAP2 and actin. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2016]","start":40040233,"end":40072649,"strand":1,"description":"cyclase associated actin cytoskeleton regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:20040]"}, {"versioned_ensembl_gene_id":"ENSG00000276996.2","gene_symbol":"SLC6A3","gene_name":"solute carrier family 6 member 3 [Source:HGNC Symbol;Acc:HGNC:11049]","synonyms":"DAT1,DAT","biotype":"protein_coding","ncbi_id":"6531","summary":"This gene encodes a dopamine transporter which is a member of the sodium- and chloride-dependent neurotransmitter transporter family. The 3' UTR of this gene contains a 40 bp tandem repeat, referred to as a variable number tandem repeat or VNTR, which can be present in 3 to 11 copies. Variation in the number of repeats is associated with idiopathic epilepsy, attention-deficit hyperactivity disorder, dependence on alcohol and cocaine, susceptibility to Parkinson disease and protection against nicotine dependence.[provided by RefSeq, Nov 2009]","start":1392790,"end":1449666,"strand":-1,"description":"solute carrier family 6 member 3 [Source:HGNC Symbol;Acc:HGNC:11049]"}, {"versioned_ensembl_gene_id":"ENSG00000262446.5","gene_symbol":"GBA","gene_name":"glucosylceramidase beta [Source:HGNC Symbol;Acc:HGNC:4177]","synonyms":"GLUC,GBA1","biotype":"protein_coding","ncbi_id":"2629","summary":"This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010]","start":155249852,"end":155260266,"strand":-1,"description":"glucosylceramidase beta [Source:HGNC Symbol;Acc:HGNC:4177]"}, {"versioned_ensembl_gene_id":"ENSG00000275015.1","gene_symbol":"AL353149.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":88259129,"end":88259372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188668.4","gene_symbol":"OR7E90P","gene_name":"olfactory receptor family 7 subfamily E member 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:14733]","synonyms":"OST705,OR7E123P","biotype":"unprocessed_pseudogene","ncbi_id":"79537","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":158874642,"end":158875670,"strand":1,"description":"olfactory receptor family 7 subfamily E member 90 pseudogene [Source:HGNC Symbol;Acc:HGNC:14733]"}, {"versioned_ensembl_gene_id":"ENSG00000233363.1","gene_symbol":"AC006019.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154092201,"end":154096043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273254.1","gene_symbol":"AF129075.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29024255,"end":29024890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177951.17","gene_symbol":"BET1L","gene_name":"Bet1 golgi vesicular membrane trafficking protein like [Source:HGNC Symbol;Acc:HGNC:19348]","synonyms":"GS15,GOLIM3","biotype":"protein_coding","ncbi_id":"51272","summary":null,"start":167784,"end":207428,"strand":-1,"description":"Bet1 golgi vesicular membrane trafficking protein like [Source:HGNC Symbol;Acc:HGNC:19348]"}, {"versioned_ensembl_gene_id":"ENSG00000131059.11","gene_symbol":"BPIFA3","gene_name":"BPI fold containing family A member 3 [Source:HGNC Symbol;Acc:HGNC:16204]","synonyms":"bA49G10.4,SPLUNC3,C20orf71","biotype":"protein_coding","ncbi_id":"128861","summary":null,"start":33217310,"end":33227758,"strand":1,"description":"BPI fold containing family A member 3 [Source:HGNC Symbol;Acc:HGNC:16204]"}, {"versioned_ensembl_gene_id":"ENSG00000107854.5","gene_symbol":"TNKS2","gene_name":"tankyrase 2 [Source:HGNC Symbol;Acc:HGNC:15677]","synonyms":"PARP5C,PARP5B,PARP-5c,PARP-5b,TNKL,TANK2,pART6","biotype":"protein_coding","ncbi_id":"80351","summary":null,"start":91798312,"end":91865276,"strand":1,"description":"tankyrase 2 [Source:HGNC Symbol;Acc:HGNC:15677]"}, {"versioned_ensembl_gene_id":"ENSG00000080572.12","gene_symbol":"PIH1D3","gene_name":"PIH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28570]","synonyms":"NYSAR97,MGC35261,CXorf41","biotype":"protein_coding","ncbi_id":"139212","summary":null,"start":107206632,"end":107244243,"strand":1,"description":"PIH1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28570]"}, {"versioned_ensembl_gene_id":"ENSG00000120251.18","gene_symbol":"GRIA2","gene_name":"glutamate ionotropic receptor AMPA type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4572]","synonyms":"GLURB,GLUR2,GluA2","biotype":"protein_coding","ncbi_id":"2891","summary":"Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to a family of glutamate receptors that are sensitive to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and function as ligand-activated cation channels. These channels are assembled from 4 related subunits, GRIA1-4. The subunit encoded by this gene (GRIA2) is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to render the channel impermeable to Ca(2+). Human and animal studies suggest that pre-mRNA editing is essential for brain function, and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology. Alternative splicing, resulting in transcript variants encoding different isoforms, (including the flip and flop isoforms that vary in their signal transduction properties), has been noted for this gene. [provided by RefSeq, Jul 2008]","start":157204182,"end":157366075,"strand":1,"description":"glutamate ionotropic receptor AMPA type subunit 2 [Source:HGNC Symbol;Acc:HGNC:4572]"}, {"versioned_ensembl_gene_id":"ENSG00000229417.1","gene_symbol":"NPM1P25","gene_name":"nucleophosmin 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:45204]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399804","summary":null,"start":96189366,"end":96190219,"strand":-1,"description":"nucleophosmin 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:45204]"}, {"versioned_ensembl_gene_id":"ENSG00000135374.9","gene_symbol":"ELF5","gene_name":"E74 like ETS transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:3320]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2001","summary":"The protein encoded by this gene is a member of an epithelium-specific subclass of the Ets transcritpion factor family. In addition to its role in regulating the later stages of terminal differentiation of keratinocytes, it appears to regulate a number of epithelium-specific genes found in tissues containing glandular epithelium such as salivary gland and prostate. It has very low affinity to DNA due to its negative regulatory domain at the amino terminus. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2011]","start":34478793,"end":34513805,"strand":-1,"description":"E74 like ETS transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:3320]"}, {"versioned_ensembl_gene_id":"ENSG00000224715.1","gene_symbol":"Z82186.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47345569,"end":47373541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254581.1","gene_symbol":"AC068587.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12676035,"end":12676389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227815.2","gene_symbol":"AL359265.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":176272483,"end":176273402,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232463.1","gene_symbol":"AL359265.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176231200,"end":176231830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232804.5","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31894767,"end":31897281,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000231526.3","gene_symbol":"HLA-DQA2","gene_name":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]","synonyms":"HLA-DXA","biotype":"protein_coding","ncbi_id":"3118","summary":"This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010]","start":32832954,"end":32838824,"strand":1,"description":"major histocompatibility complex, class II, DQ alpha 2 [Source:HGNC Symbol;Acc:HGNC:4943]"}, {"versioned_ensembl_gene_id":"ENSG00000149658.17","gene_symbol":"YTHDF1","gene_name":"YTH N6-methyladenosine RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:15867]","synonyms":"FLJ20391,C20orf21","biotype":"protein_coding","ncbi_id":"54915","summary":null,"start":63195429,"end":63216234,"strand":-1,"description":"YTH N6-methyladenosine RNA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:15867]"}, {"versioned_ensembl_gene_id":"ENSG00000259933.6","gene_symbol":"AC009065.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":2091436,"end":2095433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111011.17","gene_symbol":"RSRC2","gene_name":"arginine and serine rich coiled-coil 2 [Source:HGNC Symbol;Acc:HGNC:30559]","synonyms":"FLJ11021","biotype":"protein_coding","ncbi_id":"65117","summary":null,"start":122503458,"end":122527000,"strand":-1,"description":"arginine and serine rich coiled-coil 2 [Source:HGNC Symbol;Acc:HGNC:30559]"}, {"versioned_ensembl_gene_id":"ENSG00000262171.1","gene_symbol":"AC130651.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15885029,"end":15886158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000069667.15","gene_symbol":"RORA","gene_name":"RAR related orphan receptor A [Source:HGNC Symbol;Acc:HGNC:10258]","synonyms":"RZRA,ROR3,ROR2,ROR1,NR1F1","biotype":"protein_coding","ncbi_id":"6095","summary":"The protein encoded by this gene is a member of the NR1 subfamily of nuclear hormone receptors. It can bind as a monomer or as a homodimer to hormone response elements upstream of several genes to enhance the expression of those genes. The encoded protein has been shown to interact with NM23-2, a nucleoside diphosphate kinase involved in organogenesis and differentiation, as well as with NM23-1, the product of a tumor metastasis suppressor candidate gene. Also, it has been shown to aid in the transcriptional regulation of some genes involved in circadian rhythm. Four transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2014]","start":60488284,"end":61229319,"strand":-1,"description":"RAR related orphan receptor A [Source:HGNC Symbol;Acc:HGNC:10258]"}, {"versioned_ensembl_gene_id":"ENSG00000236339.1","gene_symbol":"POM121L13P","gene_name":"POM121 transmembrane nucleoporin like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:42635]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874379","summary":null,"start":28778558,"end":28778937,"strand":1,"description":"POM121 transmembrane nucleoporin like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:42635]"}, {"versioned_ensembl_gene_id":"ENSG00000134070.4","gene_symbol":"IRAK2","gene_name":"interleukin 1 receptor associated kinase 2 [Source:HGNC Symbol;Acc:HGNC:6113]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3656","summary":"IRAK2 encodes the interleukin-1 receptor-associated kinase 2, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. IRAK2 is reported to participate in the IL1-induced upregulation of NF-kappaB. [provided by RefSeq, Jul 2008]","start":10164865,"end":10243743,"strand":1,"description":"interleukin 1 receptor associated kinase 2 [Source:HGNC Symbol;Acc:HGNC:6113]"}, {"versioned_ensembl_gene_id":"ENSG00000226822.2","gene_symbol":"AL390036.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108040263,"end":108076020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236021.1","gene_symbol":"AL359265.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176207648,"end":176229330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186312.10","gene_symbol":"CA5BP1","gene_name":"carbonic anhydrase 5B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29544]","synonyms":"PRO2325,CA5BP,CA5BL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"340591","summary":null,"start":15674932,"end":15703724,"strand":1,"description":"carbonic anhydrase 5B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29544]"}, {"versioned_ensembl_gene_id":"ENSG00000253712.1","gene_symbol":"AC022274.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75167704,"end":75176656,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196150.13","gene_symbol":"ZNF250","gene_name":"zinc finger protein 250 [Source:HGNC Symbol;Acc:HGNC:13044]","synonyms":"ZNF647,ZFP647,MGC9718","biotype":"protein_coding","ncbi_id":"58500","summary":null,"start":144876497,"end":144902168,"strand":-1,"description":"zinc finger protein 250 [Source:HGNC Symbol;Acc:HGNC:13044]"}, {"versioned_ensembl_gene_id":"ENSG00000236732.1","gene_symbol":"AC094019.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32151083,"end":32151895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274107.2","gene_symbol":"CR854858.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":13215394,"end":13218160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282115.1","gene_symbol":"AC015849.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35861093,"end":35861566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253374.5","gene_symbol":"AC023644.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":81521618,"end":81533275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238272.1","gene_symbol":"AL139142.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":173555251,"end":173612772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112118.18","gene_symbol":"MCM3","gene_name":"minichromosome maintenance complex component 3 [Source:HGNC Symbol;Acc:HGNC:6945]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4172","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein is a subunit of the protein complex that consists of MCM2-7. It has been shown to interact directly with MCM5/CDC46. This protein also interacts with and is acetylated by MCM3AP, a chromatin-associated acetyltransferase. The acetylation of this protein inhibits the initiation of DNA replication and cell cycle progression. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2018]","start":52264009,"end":52284881,"strand":-1,"description":"minichromosome maintenance complex component 3 [Source:HGNC Symbol;Acc:HGNC:6945]"}, {"versioned_ensembl_gene_id":"ENSG00000274750.2","gene_symbol":"HIST1H3E","gene_name":"histone cluster 1 H3 family member e [Source:HGNC Symbol;Acc:HGNC:4769]","synonyms":"H3FD,H3/d,H3.1","biotype":"protein_coding","ncbi_id":"8353","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]","start":26224199,"end":26227473,"strand":1,"description":"histone cluster 1 H3 family member e [Source:HGNC Symbol;Acc:HGNC:4769]"}, {"versioned_ensembl_gene_id":"ENSG00000275760.4","gene_symbol":"TBC1D3G","gene_name":"TBC1 domain family member 3G [Source:HGNC Symbol;Acc:HGNC:29860]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060321","summary":null,"start":36324256,"end":36335131,"strand":1,"description":"TBC1 domain family member 3G [Source:HGNC Symbol;Acc:HGNC:29860]"}, {"versioned_ensembl_gene_id":"ENSG00000241305.1","gene_symbol":"ACTG1P13","gene_name":"actin gamma 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49058]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418920","summary":null,"start":99215224,"end":99216266,"strand":-1,"description":"actin gamma 1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49058]"}, {"versioned_ensembl_gene_id":"ENSG00000168522.12","gene_symbol":"FNTA","gene_name":"farnesyltransferase, CAAX box, alpha [Source:HGNC Symbol;Acc:HGNC:3782]","synonyms":"PTAR2,PGGT1A,FPTA","biotype":"protein_coding","ncbi_id":"2339","summary":"Prenyltransferases can attach either a farnesyl group or a geranylgeranyl group in thioether linkage to the cysteine residue of proteins with a C-terminal CAAX box. CAAX geranylgeranyltransferase and CAAX farnesyltransferase are heterodimers that share the same alpha subunit but have different beta subunits. This gene encodes the alpha subunit of these transferases. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 11 and 13. [provided by RefSeq, May 2010]","start":43034194,"end":43085788,"strand":1,"description":"farnesyltransferase, CAAX box, alpha [Source:HGNC Symbol;Acc:HGNC:3782]"}, {"versioned_ensembl_gene_id":"ENSG00000228784.7","gene_symbol":"LINC00954","gene_name":"long intergenic non-protein coding RNA 954 [Source:HGNC Symbol;Acc:HGNC:48668]","synonyms":"FLJ12334","biotype":"lincRNA","ncbi_id":"400946","summary":null,"start":19868860,"end":19885047,"strand":1,"description":"long intergenic non-protein coding RNA 954 [Source:HGNC Symbol;Acc:HGNC:48668]"}, {"versioned_ensembl_gene_id":"ENSG00000185385.4","gene_symbol":"OR7A17","gene_name":"olfactory receptor family 7 subfamily A member 17 [Source:HGNC Symbol;Acc:HGNC:8363]","synonyms":"HTPCRX19","biotype":"protein_coding","ncbi_id":"26333","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14878203,"end":14886132,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 17 [Source:HGNC Symbol;Acc:HGNC:8363]"}, {"versioned_ensembl_gene_id":"ENSG00000150175.13","gene_symbol":"FRMPD2B","gene_name":"FERM and PDZ domain containing 2B, pseudogene [Source:HGNC Symbol;Acc:HGNC:16843]","synonyms":"FRMPD2P1,FRMPD2L2,FRMPD2L1,bA556L1.2,yX59F3.2,PDZK5B,PDZK5A,PDZD5B,PDZD5A,FRMPD2P2","biotype":"unprocessed_pseudogene","ncbi_id":"728798","summary":"This gene represents a pseudogene of the FERM and PDZ domain containing 2 gene (FRMPD2, GeneID 143162). Along with the functional gene, this gene is located in a region of segmental duplication on chromosome 10q. [provided by RefSeq, Dec 2014]","start":46870858,"end":46894562,"strand":1,"description":"FERM and PDZ domain containing 2B, pseudogene [Source:HGNC Symbol;Acc:HGNC:16843]"}, {"versioned_ensembl_gene_id":"ENSG00000236968.1","gene_symbol":"AL451164.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3223816,"end":3227407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256011.1","gene_symbol":"AC007688.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12962300,"end":12963539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223975.1","gene_symbol":"AP001048.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43465309,"end":43467298,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171862.10","gene_symbol":"PTEN","gene_name":"phosphatase and tensin homolog [Source:HGNC Symbol;Acc:HGNC:9588]","synonyms":"TEP1,PTEN1,MMAC1,MHAM,BZS","biotype":"protein_coding","ncbi_id":"5728","summary":"This gene was identified as a tumor suppressor that is mutated in a large number of cancers at high frequency. The protein encoded by this gene is a phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase. It contains a tensin like domain as well as a catalytic domain similar to that of the dual specificity protein tyrosine phosphatases. Unlike most of the protein tyrosine phosphatases, this protein preferentially dephosphorylates phosphoinositide substrates. It negatively regulates intracellular levels of phosphatidylinositol-3,4,5-trisphosphate in cells and functions as a tumor suppressor by negatively regulating AKT/PKB signaling pathway. The use of a non-canonical (CUG) upstream initiation site produces a longer isoform that initiates translation with a leucine, and is thought to be preferentially associated with the mitochondrial inner membrane. This longer isoform may help regulate energy metabolism in the mitochondria. A pseudogene of this gene is found on chromosome 9. Alternative splicing and the use of multiple translation start codons results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]","start":87863113,"end":87971930,"strand":1,"description":"phosphatase and tensin homolog [Source:HGNC Symbol;Acc:HGNC:9588]"}, {"versioned_ensembl_gene_id":"ENSG00000149927.17","gene_symbol":"DOC2A","gene_name":"double C2 domain alpha [Source:HGNC Symbol;Acc:HGNC:2985]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8448","summary":"There are at least two protein isoforms of the Double C2 protein, namely alpha (DOC2A) and beta (DOC2B), which contain two C2-like domains. DOC2A and DOC2B are encoded by different genes; these genes are at times confused with the unrelated DAB2 gene which was initially named DOC-2. DOC2A is mainly expressed in brain and is suggested to be involved in Ca(2+)-dependent neurotransmitter release. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":30005509,"end":30023270,"strand":-1,"description":"double C2 domain alpha [Source:HGNC Symbol;Acc:HGNC:2985]"}, {"versioned_ensembl_gene_id":"ENSG00000211789.2","gene_symbol":"TRAV12-2","gene_name":"T-cell receptor alpha variable 12-2 [Source:HGNC Symbol;Acc:HGNC:12106]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28673","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21887857,"end":21888502,"strand":1,"description":"T-cell receptor alpha variable 12-2 [Source:HGNC Symbol;Acc:HGNC:12106]"}, {"versioned_ensembl_gene_id":"ENSG00000121577.13","gene_symbol":"POPDC2","gene_name":"popeye domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17648]","synonyms":"POP2","biotype":"protein_coding","ncbi_id":"64091","summary":"This gene encodes a member of the POP family of proteins which contain three putative transmembrane domains. This membrane associated protein is predominantly expressed in skeletal and cardiac muscle, and may have an important function in these tissues. [provided by RefSeq, Jul 2008]","start":119636457,"end":119665324,"strand":-1,"description":"popeye domain containing 2 [Source:HGNC Symbol;Acc:HGNC:17648]"}, {"versioned_ensembl_gene_id":"ENSG00000075303.12","gene_symbol":"SLC25A40","gene_name":"solute carrier family 25 member 40 [Source:HGNC Symbol;Acc:HGNC:29680]","synonyms":"MCFP","biotype":"protein_coding","ncbi_id":"55972","summary":"SLC25A40 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":87833568,"end":87876357,"strand":-1,"description":"solute carrier family 25 member 40 [Source:HGNC Symbol;Acc:HGNC:29680]"}, {"versioned_ensembl_gene_id":"ENSG00000128510.10","gene_symbol":"CPA4","gene_name":"carboxypeptidase A4 [Source:HGNC Symbol;Acc:HGNC:15740]","synonyms":"CPA3","biotype":"protein_coding","ncbi_id":"51200","summary":"This gene is a member of the carboxypeptidase A/B subfamily, and it is located in a cluster with three other family members on chromosome 7. Carboxypeptidases are zinc-containing exopeptidases that catalyze the release of carboxy-terminal amino acids, and are synthesized as zymogens that are activated by proteolytic cleavage. This gene could be involved in the histone hyperacetylation pathway. It is imprinted and may be a strong candidate gene for prostate cancer aggressiveness. [provided by RefSeq, Jul 2008]","start":130293134,"end":130324180,"strand":1,"description":"carboxypeptidase A4 [Source:HGNC Symbol;Acc:HGNC:15740]"}, {"versioned_ensembl_gene_id":"ENSG00000270074.1","gene_symbol":"AC087203.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12412827,"end":12414373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137216.18","gene_symbol":"TMEM63B","gene_name":"transmembrane protein 63B [Source:HGNC Symbol;Acc:HGNC:17735]","synonyms":"DKFZp434P0531,dJ421H19.2,C6orf110","biotype":"protein_coding","ncbi_id":"55362","summary":null,"start":44126914,"end":44155519,"strand":1,"description":"transmembrane protein 63B [Source:HGNC Symbol;Acc:HGNC:17735]"}, {"versioned_ensembl_gene_id":"ENSG00000127511.9","gene_symbol":"SIN3B","gene_name":"SIN3 transcription regulator family member B [Source:HGNC Symbol;Acc:HGNC:19354]","synonyms":"KIAA0700","biotype":"protein_coding","ncbi_id":"23309","summary":null,"start":16829400,"end":16880353,"strand":1,"description":"SIN3 transcription regulator family member B [Source:HGNC Symbol;Acc:HGNC:19354]"}, {"versioned_ensembl_gene_id":"ENSG00000211777.2","gene_symbol":"TRAV3","gene_name":"T-cell receptor alpha variable 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12128]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28690","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21723713,"end":21724321,"strand":1,"description":"T-cell receptor alpha variable 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12128]"}, {"versioned_ensembl_gene_id":"ENSG00000215097.3","gene_symbol":"DUSP8P3","gene_name":"dual specificity phosphatase 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3077]","synonyms":"HVH4,DUSPP","biotype":"processed_pseudogene","ncbi_id":"441554","summary":null,"start":46774421,"end":46776180,"strand":-1,"description":"dual specificity phosphatase 8 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:3077]"}, {"versioned_ensembl_gene_id":"ENSG00000229459.1","gene_symbol":"AC023669.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46261064,"end":46294469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237760.1","gene_symbol":"AC023669.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46302120,"end":46343621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124496.12","gene_symbol":"TRERF1","gene_name":"transcriptional regulating factor 1 [Source:HGNC Symbol;Acc:HGNC:18273]","synonyms":"TReP-132,RAPA,HSA277276,dJ139D8.5,BCAR2","biotype":"protein_coding","ncbi_id":"55809","summary":"This gene encodes a zinc-finger transcriptional regulating protein which interacts with CBP/p300 to regulate the human gene CYP11A1. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]","start":42224931,"end":42452051,"strand":-1,"description":"transcriptional regulating factor 1 [Source:HGNC Symbol;Acc:HGNC:18273]"}, {"versioned_ensembl_gene_id":"ENSG00000238124.1","gene_symbol":"AC114501.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65463071,"end":65463438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186716.20","gene_symbol":"BCR","gene_name":"BCR, RhoGEF and GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:1014]","synonyms":"PHL,D22S662,D22S11,CML,BCR1,ALL","biotype":"protein_coding","ncbi_id":"613","summary":"A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The unregulated tyrosine kinase activity of BCR-ABL1 contributes to the immortality of leukaemic cells. The BCR protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac and other kinases. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2020]","start":23179704,"end":23318037,"strand":1,"description":"BCR, RhoGEF and GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:1014]"}, {"versioned_ensembl_gene_id":"ENSG00000105948.13","gene_symbol":"TTC26","gene_name":"tetratricopeptide repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:21882]","synonyms":"dyf-13,IFT56,FLJ12571,DYF13","biotype":"protein_coding","ncbi_id":"79989","summary":null,"start":139133744,"end":139191986,"strand":1,"description":"tetratricopeptide repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:21882]"}, {"versioned_ensembl_gene_id":"ENSG00000100078.3","gene_symbol":"PLA2G3","gene_name":"phospholipase A2 group III [Source:HGNC Symbol;Acc:HGNC:17934]","synonyms":"GIII-SPLA2","biotype":"protein_coding","ncbi_id":"50487","summary":"This gene encodes a protein that belongs to the secreted phospholipase A2 family, whose members include the bee venom enzyme. The encoded enzyme functions in lipid metabolism and catalyzes the calcium-dependent hydrolysis of the sn-2 acyl bond of phospholipids to release arachidonic acid and lysophospholipids. This enzyme acts as a negative regulator of ciliogenesis, and may play a role in cancer development by stimulating tumor cell growth and angiogenesis. This gene is associated with oxidative stress, and polymorphisms in this gene are linked to risk for Alzheimer's disease. [provided by RefSeq, Apr 2014]","start":31134809,"end":31140607,"strand":-1,"description":"phospholipase A2 group III [Source:HGNC Symbol;Acc:HGNC:17934]"}, {"versioned_ensembl_gene_id":"ENSG00000267396.1","gene_symbol":"AC090236.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58398663,"end":58400082,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231167.3","gene_symbol":"YBX1P2","gene_name":"Y-box binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22635]","synonyms":"TCAG_1818537","biotype":"processed_pseudogene","ncbi_id":"646531","summary":null,"start":105582258,"end":105583256,"strand":-1,"description":"Y-box binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22635]"}, {"versioned_ensembl_gene_id":"ENSG00000224626.1","gene_symbol":"AC106053.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18784807,"end":18787752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231680.1","gene_symbol":"AP003774.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64394342,"end":64395831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224330.1","gene_symbol":"AC005019.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13854355,"end":13859025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000001460.17","gene_symbol":"STPG1","gene_name":"sperm tail PG-rich repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:28070]","synonyms":"MAPO2,FLJ33340,C1orf201","biotype":"protein_coding","ncbi_id":"90529","summary":null,"start":24356999,"end":24416934,"strand":-1,"description":"sperm tail PG-rich repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:28070]"}, {"versioned_ensembl_gene_id":"ENSG00000100298.15","gene_symbol":"APOBEC3H","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3H [Source:HGNC Symbol;Acc:HGNC:24100]","synonyms":"ARP10","biotype":"protein_coding","ncbi_id":"164668","summary":"This gene encodes a member of the apolipoprotein B mRNA-editing enzyme catalytic polypeptide 3 family of proteins. The encoded protein is a cytidine deaminase that has antiretroviral activity by generating lethal hypermutations in viral genomes. Polymorphisms and alternative splicing in this gene influence its antiretroviral activity and are associated with increased resistence to human immunodeficiency virus type 1 infection in certain populations. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":39097224,"end":39104067,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 3H [Source:HGNC Symbol;Acc:HGNC:24100]"}, {"versioned_ensembl_gene_id":"ENSG00000230879.1","gene_symbol":"RBMX2P4","gene_name":"RNA binding motif protein, X-linked 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862677","summary":null,"start":12922545,"end":12922920,"strand":-1,"description":"RNA binding motif protein, X-linked 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39926]"}, {"versioned_ensembl_gene_id":"ENSG00000101951.16","gene_symbol":"PAGE4","gene_name":"PAGE family member 4 [Source:HGNC Symbol;Acc:HGNC:4108]","synonyms":"PAGE-4,GAGEC1,CT16.7","biotype":"protein_coding","ncbi_id":"9506","summary":"This gene is a member of the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. This gene is strongly expressed in prostate and prostate cancer. It is also expressed in other male and female reproductive tissues including testis, fallopian tube, uterus, and placenta, as well as in testicular cancer and uterine cancer. The protein encoded by this gene shares sequence similarity with other GAGE/PAGE proteins, and also belongs to a family of CT (cancer-testis) antigens. The protein may play a role in benign and malignant prostate diseases. A related pseudogene is located on chromosome 7. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":49829260,"end":49833973,"strand":1,"description":"PAGE family member 4 [Source:HGNC Symbol;Acc:HGNC:4108]"}, {"versioned_ensembl_gene_id":"ENSG00000243780.1","gene_symbol":"AC092754.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59525422,"end":59525881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234576.1","gene_symbol":"MTND1P26","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42075]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873214","summary":null,"start":131385700,"end":131386237,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:42075]"}, {"versioned_ensembl_gene_id":"ENSG00000257784.1","gene_symbol":"LINC02400","gene_name":"long intergenic non-protein coding RNA 2400 [Source:HGNC Symbol;Acc:HGNC:53327]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927038","summary":null,"start":41764189,"end":41765581,"strand":1,"description":"long intergenic non-protein coding RNA 2400 [Source:HGNC Symbol;Acc:HGNC:53327]"}, {"versioned_ensembl_gene_id":"ENSG00000277844.1","gene_symbol":"AC087382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":66290635,"end":66291180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167700.8","gene_symbol":"MFSD3","gene_name":"major facilitator superfamily domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25157]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113655","summary":null,"start":144509074,"end":144511213,"strand":1,"description":"major facilitator superfamily domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25157]"}, {"versioned_ensembl_gene_id":"ENSG00000198064.13","gene_symbol":"NPIPB13","gene_name":"nuclear pore complex interacting protein family, member B13 [Source:HGNC Symbol;Acc:HGNC:41989]","synonyms":null,"biotype":"protein_coding","ncbi_id":"613037","summary":null,"start":30222937,"end":30254510,"strand":-1,"description":"nuclear pore complex interacting protein family, member B13 [Source:HGNC Symbol;Acc:HGNC:41989]"}, {"versioned_ensembl_gene_id":"ENSG00000106080.10","gene_symbol":"FKBP14","gene_name":"FK506 binding protein 14 [Source:HGNC Symbol;Acc:HGNC:18625]","synonyms":"FLJ20731,FKBP22","biotype":"protein_coding","ncbi_id":"55033","summary":"The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012]","start":30010587,"end":30026684,"strand":-1,"description":"FK506 binding protein 14 [Source:HGNC Symbol;Acc:HGNC:18625]"}, {"versioned_ensembl_gene_id":"ENSG00000230023.2","gene_symbol":"AL590683.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24200240,"end":24211693,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261203.1","gene_symbol":"AC106782.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30218220,"end":30221930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196456.11","gene_symbol":"ZNF775","gene_name":"zinc finger protein 775 [Source:HGNC Symbol;Acc:HGNC:28501]","synonyms":"MGC33584","biotype":"protein_coding","ncbi_id":"285971","summary":null,"start":150379335,"end":150398631,"strand":1,"description":"zinc finger protein 775 [Source:HGNC Symbol;Acc:HGNC:28501]"}, {"versioned_ensembl_gene_id":"ENSG00000115318.11","gene_symbol":"LOXL3","gene_name":"lysyl oxidase like 3 [Source:HGNC Symbol;Acc:HGNC:13869]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84695","summary":"This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]","start":74532414,"end":74555690,"strand":-1,"description":"lysyl oxidase like 3 [Source:HGNC Symbol;Acc:HGNC:13869]"}, {"versioned_ensembl_gene_id":"ENSG00000184650.10","gene_symbol":"ODF4","gene_name":"outer dense fiber of sperm tails 4 [Source:HGNC Symbol;Acc:HGNC:19056]","synonyms":"OPPO1,CT136","biotype":"protein_coding","ncbi_id":"146852","summary":"This gene encodes a protein that is localized in the outer dense fibers of the tails of mature sperm. This protein is thought to have some important role in the sperm tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":8339864,"end":8346048,"strand":1,"description":"outer dense fiber of sperm tails 4 [Source:HGNC Symbol;Acc:HGNC:19056]"}, {"versioned_ensembl_gene_id":"ENSG00000225930.3","gene_symbol":"LINC02249","gene_name":"long intergenic non-protein coding RNA 2249 [Source:HGNC Symbol;Acc:HGNC:32351]","synonyms":"DKFZp434L187","biotype":"lincRNA","ncbi_id":"26082","summary":null,"start":30196036,"end":30214540,"strand":1,"description":"long intergenic non-protein coding RNA 2249 [Source:HGNC Symbol;Acc:HGNC:32351]"}, {"versioned_ensembl_gene_id":"ENSG00000166948.9","gene_symbol":"TGM6","gene_name":"transglutaminase 6 [Source:HGNC Symbol;Acc:HGNC:16255]","synonyms":"dJ734P14.3,TGY,TGM3L,SCA35","biotype":"protein_coding","ncbi_id":"343641","summary":"The protein encoded by this gene belongs to the transglutaminase superfamily. It catalyzes the cross-linking of proteins and the conjugation of polyamines to proteins. Mutations in this gene are associated with spinocerebellar ataxia type 35 (SCA35). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":2380908,"end":2432753,"strand":1,"description":"transglutaminase 6 [Source:HGNC Symbol;Acc:HGNC:16255]"}, {"versioned_ensembl_gene_id":"ENSG00000160678.11","gene_symbol":"S100A1","gene_name":"S100 calcium binding protein A1 [Source:HGNC Symbol;Acc:HGNC:10486]","synonyms":"S100A,S100-alpha","biotype":"protein_coding","ncbi_id":"6271","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in stimulation of Ca2+-induced Ca2+ release, inhibition of microtubule assembly, and inhibition of protein kinase C-mediated phosphorylation. Reduced expression of this protein has been implicated in cardiomyopathies. [provided by RefSeq, Jul 2008]","start":153627926,"end":153632039,"strand":1,"description":"S100 calcium binding protein A1 [Source:HGNC Symbol;Acc:HGNC:10486]"}, {"versioned_ensembl_gene_id":"ENSG00000266102.1","gene_symbol":"AP006219.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10375103,"end":10378114,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172850.11","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"G7b,C6orf28,YBL026W","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31787629,"end":31797209,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000255525.1","gene_symbol":"AL137804.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31305685,"end":31314548,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250442.1","gene_symbol":"EIF3KP3","gene_name":"eukaryotic translation initiation factor 3 subunit K pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44018]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645368","summary":null,"start":116043407,"end":116044045,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit K pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44018]"}, {"versioned_ensembl_gene_id":"ENSG00000267642.1","gene_symbol":"AC091198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33552123,"end":33578187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255370.1","gene_symbol":"CYCSP25","gene_name":"cytochrome c, somatic pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:24399]","synonyms":"HCP25,HC10","biotype":"processed_pseudogene","ncbi_id":"120528","summary":null,"start":31280672,"end":31280987,"strand":-1,"description":"cytochrome c, somatic pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:24399]"}, {"versioned_ensembl_gene_id":"ENSG00000153237.17","gene_symbol":"CCDC148","gene_name":"coiled-coil domain containing 148 [Source:HGNC Symbol;Acc:HGNC:25191]","synonyms":"MGC125588","biotype":"protein_coding","ncbi_id":"130940","summary":null,"start":158171081,"end":158456753,"strand":-1,"description":"coiled-coil domain containing 148 [Source:HGNC Symbol;Acc:HGNC:25191]"}, {"versioned_ensembl_gene_id":"ENSG00000228302.2","gene_symbol":"AL512770.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12244751,"end":12247845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155099.7","gene_symbol":"TMEM55A","gene_name":"transmembrane protein 55A [Source:HGNC Symbol;Acc:HGNC:25452]","synonyms":"DKFZp762O076","biotype":"protein_coding","ncbi_id":"55529","summary":"TMEM55A catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]","start":90993796,"end":91041064,"strand":-1,"description":"transmembrane protein 55A [Source:HGNC Symbol;Acc:HGNC:25452]"}, {"versioned_ensembl_gene_id":"ENSG00000164972.12","gene_symbol":"C9orf24","gene_name":"chromosome 9 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:19919]","synonyms":"SMRP1,NYD-SP22,MGC33614,MGC32921,CBE1,bA573M23.4","biotype":"protein_coding","ncbi_id":"84688","summary":"This gene encodes a nuclear- or perinuclear-localized protein with no predicted domains or similarity to other known proteins. Expression of this gene is induced during the differentiation of bronchial epithelial cells, and the encoded protein may play a role in ciliogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]","start":34379019,"end":34397832,"strand":-1,"description":"chromosome 9 open reading frame 24 [Source:HGNC Symbol;Acc:HGNC:19919]"}, {"versioned_ensembl_gene_id":"ENSG00000250748.6","gene_symbol":"AC025419.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":65466820,"end":65642372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260706.5","gene_symbol":"AC022166.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80065836,"end":80167577,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249454.1","gene_symbol":"GZMAP1","gene_name":"granzyme A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44137]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479035","summary":null,"start":55073015,"end":55096553,"strand":1,"description":"granzyme A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44137]"}, {"versioned_ensembl_gene_id":"ENSG00000189334.8","gene_symbol":"S100A14","gene_name":"S100 calcium binding protein A14 [Source:HGNC Symbol;Acc:HGNC:18901]","synonyms":"S100A15,BCMP84","biotype":"protein_coding","ncbi_id":"57402","summary":"This gene encodes a member of the S100 protein family which contains an EF-hand motif and binds calcium. The gene is located in a cluster of S100 genes on chromosome 1. Levels of the encoded protein have been found to be lower in cancerous tissue and associated with metastasis suggesting a tumor suppressor function (PMID: 19956863, 19351828). [provided by RefSeq, Dec 2011]","start":153614255,"end":153616986,"strand":-1,"description":"S100 calcium binding protein A14 [Source:HGNC Symbol;Acc:HGNC:18901]"}, {"versioned_ensembl_gene_id":"ENSG00000243978.8","gene_symbol":"RTL9","gene_name":"retrotransposon Gag like 9 [Source:HGNC Symbol;Acc:HGNC:29245]","synonyms":"SIRH10,RGAG1,Mart9,Mar9,KIAA1318","biotype":"protein_coding","ncbi_id":"57529","summary":null,"start":110358816,"end":110456334,"strand":1,"description":"retrotransposon Gag like 9 [Source:HGNC Symbol;Acc:HGNC:29245]"}, {"versioned_ensembl_gene_id":"ENSG00000241101.1","gene_symbol":"PRICKLE2-AS2","gene_name":"PRICKLE2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40917]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874242","summary":null,"start":64103470,"end":64106056,"strand":1,"description":"PRICKLE2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40917]"}, {"versioned_ensembl_gene_id":"ENSG00000249479.1","gene_symbol":"AC096736.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156642580,"end":156643569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251376.1","gene_symbol":"AC034238.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55054428,"end":55055140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224985.1","gene_symbol":"AL590714.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161153760,"end":161159349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228670.4","gene_symbol":"NANOGP2","gene_name":"Nanog homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23100]","synonyms":"NANOGP4","biotype":"processed_pseudogene","ncbi_id":"414131","summary":null,"start":222452400,"end":222453126,"strand":-1,"description":"Nanog homeobox pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:23100]"}, {"versioned_ensembl_gene_id":"ENSG00000230155.6","gene_symbol":"FO393401.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35476203,"end":35490982,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242295.1","gene_symbol":"AC087477.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96448154,"end":96448493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258111.1","gene_symbol":"AC079316.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104514029,"end":104514439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280542.1","gene_symbol":"AC208585.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17732440,"end":17742196,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111711.9","gene_symbol":"GOLT1B","gene_name":"golgi transport 1B [Source:HGNC Symbol;Acc:HGNC:20175]","synonyms":"YMR292W,GOT1,CGI-141","biotype":"protein_coding","ncbi_id":"51026","summary":null,"start":21501781,"end":21518408,"strand":1,"description":"golgi transport 1B [Source:HGNC Symbol;Acc:HGNC:20175]"}, {"versioned_ensembl_gene_id":"ENSG00000217897.2","gene_symbol":"HSPE1P8","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100292290","summary":null,"start":39304294,"end":39304898,"strand":-1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49326]"}, {"versioned_ensembl_gene_id":"ENSG00000204396.10","gene_symbol":"VWA7","gene_name":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]","synonyms":"G7c,C6orf27,NG37","biotype":"protein_coding","ncbi_id":"80737","summary":null,"start":31765590,"end":31777294,"strand":-1,"description":"von Willebrand factor A domain containing 7 [Source:HGNC Symbol;Acc:HGNC:13939]"}, {"versioned_ensembl_gene_id":"ENSG00000186496.10","gene_symbol":"ZNF396","gene_name":"zinc finger protein 396 [Source:HGNC Symbol;Acc:HGNC:18824]","synonyms":"ZSCAN14,FLJ31213","biotype":"protein_coding","ncbi_id":"252884","summary":null,"start":35366697,"end":35377337,"strand":-1,"description":"zinc finger protein 396 [Source:HGNC Symbol;Acc:HGNC:18824]"}, {"versioned_ensembl_gene_id":"ENSG00000262635.5","gene_symbol":"TDO2","gene_name":"tryptophan 2,3-dioxygenase [Source:HGNC Symbol;Acc:HGNC:11708]","synonyms":"TPH2,TDO","biotype":"protein_coding","ncbi_id":"6999","summary":"This gene encodes a heme enzyme that plays a critical role in tryptophan metabolism by catalyzing the first and rate-limiting step of the kynurenine pathway. Increased activity of the encoded protein and subsequent kynurenine production may also play a role in cancer through the suppression of antitumor immune responses, and single nucleotide polymorphisms in this gene may be associated with autism. [provided by RefSeq, Feb 2012]","start":155854738,"end":155920406,"strand":1,"description":"tryptophan 2,3-dioxygenase [Source:HGNC Symbol;Acc:HGNC:11708]"}, {"versioned_ensembl_gene_id":"ENSG00000257624.1","gene_symbol":"AC004024.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112000739,"end":112000985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260224.1","gene_symbol":"UBL5P4","gene_name":"ubiquitin like 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44642]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480800","summary":null,"start":11968508,"end":11968743,"strand":-1,"description":"ubiquitin like 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44642]"}, {"versioned_ensembl_gene_id":"ENSG00000198658.4","gene_symbol":"ABHD17AP1","gene_name":"abhydrolase domain containing 17A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28394]","synonyms":"FAM108A3P,FAM108A3,FAM108A2,FAM108A11P,C1orf47,ABHD17AP2","biotype":"unprocessed_pseudogene","ncbi_id":"728917","summary":null,"start":148146395,"end":148149566,"strand":1,"description":"abhydrolase domain containing 17A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28394]"}, {"versioned_ensembl_gene_id":"ENSG00000267515.1","gene_symbol":"AP001029.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12450447,"end":12451042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125414.18","gene_symbol":"MYH2","gene_name":"myosin heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:7572]","synonyms":"MyHC-2A,MYHas8,MYH2A,IBM3,MYHSA2,MyHC-IIa","biotype":"protein_coding","ncbi_id":"4620","summary":"Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in inclusion body myopathy-3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2009]","start":10521148,"end":10549957,"strand":-1,"description":"myosin heavy chain 2 [Source:HGNC Symbol;Acc:HGNC:7572]"}, {"versioned_ensembl_gene_id":"ENSG00000262133.1","gene_symbol":"AC087392.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":877902,"end":880093,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263017.1","gene_symbol":"AC036164.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":959034,"end":959366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214970.8","gene_symbol":"AC005323.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10579040,"end":10623036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277458.1","gene_symbol":"AC007216.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11926199,"end":11926307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224157.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"antisense_RNA","ncbi_id":"414760","summary":null,"start":28896530,"end":28897322,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000237591.1","gene_symbol":"HLA-DRB9","gene_name":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]","synonyms":"D6S206,HLA-DR1BL,D6S206E,HLA-DRB1L","biotype":"unprocessed_pseudogene","ncbi_id":"3132","summary":null,"start":32434517,"end":32448172,"strand":-1,"description":"major histocompatibility complex, class II, DR beta 9 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4957]"}, {"versioned_ensembl_gene_id":"ENSG00000198270.12","gene_symbol":"TMEM116","gene_name":"transmembrane protein 116 [Source:HGNC Symbol;Acc:HGNC:25084]","synonyms":"FLJ90167","biotype":"protein_coding","ncbi_id":"89894","summary":null,"start":111931282,"end":112013185,"strand":-1,"description":"transmembrane protein 116 [Source:HGNC Symbol;Acc:HGNC:25084]"}, {"versioned_ensembl_gene_id":"ENSG00000249304.1","gene_symbol":"AC104779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113943256,"end":113944320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164283.12","gene_symbol":"ESM1","gene_name":"endothelial cell specific molecule 1 [Source:HGNC Symbol;Acc:HGNC:3466]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11082","summary":"This gene encodes a secreted protein which is mainly expressed in the endothelial cells in human lung and kidney tissues. The expression of this gene is regulated by cytokines, suggesting that it may play a role in endothelium-dependent pathological disorders. The transcript contains multiple polyadenylation and mRNA instability signals. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":54977864,"end":55022671,"strand":-1,"description":"endothelial cell specific molecule 1 [Source:HGNC Symbol;Acc:HGNC:3466]"}, {"versioned_ensembl_gene_id":"ENSG00000162604.12","gene_symbol":"TM2D1","gene_name":"TM2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24142]","synonyms":"BBP","biotype":"protein_coding","ncbi_id":"83941","summary":"The protein encoded by this gene is a beta-amyloid peptide-binding protein. It contains a structural module related to that of the seven transmembrane domain G protein-coupled receptor superfamily and known to be important in heterotrimeric G protein activation. Beta-amyloid peptide has been established to be a causative factor in neuron death and the consequent diminution of cognitive abilities observed in Alzheimer's disease. This protein may be a target of neurotoxic beta-amyloid peptide, and may mediate cellular vulnerability to beta-amyloid peptide toxicity through a G protein-regulated program of cell death. Several transcript variants have been found for this gene. [provided by RefSeq, Feb 2016]","start":61681046,"end":61725423,"strand":-1,"description":"TM2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24142]"}, {"versioned_ensembl_gene_id":"ENSG00000129988.5","gene_symbol":"LBP","gene_name":"lipopolysaccharide binding protein [Source:HGNC Symbol;Acc:HGNC:6517]","synonyms":"BPIFD2","biotype":"protein_coding","ncbi_id":"3929","summary":"The protein encoded by this gene is involved in the acute-phase immunologic response to gram-negative bacterial infections. Gram-negative bacteria contain a glycolipid, lipopolysaccharide (LPS), on their outer cell wall. Together with bactericidal permeability-increasing protein (BPI), the encoded protein binds LPS and interacts with the CD14 receptor, probably playing a role in regulating LPS-dependent monocyte responses. Studies in mice suggest that the encoded protein is necessary for the rapid acute-phase response to LPS but not for the clearance of LPS from circulation. This protein is part of a family of structurally and functionally related proteins, including BPI, plasma cholesteryl ester transfer protein (CETP), and phospholipid transfer protein (PLTP). [provided by RefSeq, Apr 2012]","start":38346356,"end":38377023,"strand":1,"description":"lipopolysaccharide binding protein [Source:HGNC Symbol;Acc:HGNC:6517]"}, {"versioned_ensembl_gene_id":"ENSG00000273691.1","gene_symbol":"AC087284.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":90024955,"end":90026003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184613.10","gene_symbol":"NELL2","gene_name":"neural EGFL like 2 [Source:HGNC Symbol;Acc:HGNC:7751]","synonyms":"NRP2","biotype":"protein_coding","ncbi_id":"4753","summary":"The protein encoded by this gene is a glycoprotein containing several von Willebrand factor C domains and epidermal growth factor (EGF)-like domains. The encoded protein acts as a homotrimer and is found in the cytoplasm. Several variants encoding a few different isoforms exist, and at least one isoform appears to be a secreted protein. Studies in mouse suggest that this protein plays a role in neural cell growth and differentiation as well as in oncogenesis. [provided by RefSeq, Feb 2009]","start":44508275,"end":44921848,"strand":-1,"description":"neural EGFL like 2 [Source:HGNC Symbol;Acc:HGNC:7751]"}, {"versioned_ensembl_gene_id":"ENSG00000261552.1","gene_symbol":"AC109460.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28989140,"end":28990778,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282789.1","gene_symbol":"CRYZP1","gene_name":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"1430","summary":null,"start":103088664,"end":103089610,"strand":-1,"description":"crystallin zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2421]"}, {"versioned_ensembl_gene_id":"ENSG00000261467.2","gene_symbol":"AC099398.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73985992,"end":73988767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173905.8","gene_symbol":"GOLIM4","gene_name":"golgi integral membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:15448]","synonyms":"GOLPH4,GIMPC,P138,GPP130","biotype":"protein_coding","ncbi_id":"27333","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a type II Golgi-resident protein. It may process proteins synthesized in the rough endoplasmic reticulum and assist in the transport of protein cargo through the Golgi apparatus. [provided by RefSeq, Jul 2008]","start":168008677,"end":168095975,"strand":-1,"description":"golgi integral membrane protein 4 [Source:HGNC Symbol;Acc:HGNC:15448]"}, {"versioned_ensembl_gene_id":"ENSG00000112514.15","gene_symbol":"CUTA","gene_name":"cutA divalent cation tolerance homolog [Source:HGNC Symbol;Acc:HGNC:21101]","synonyms":"C6orf82,ACHAP","biotype":"protein_coding","ncbi_id":"51596","summary":null,"start":33416442,"end":33418317,"strand":-1,"description":"cutA divalent cation tolerance homolog [Source:HGNC Symbol;Acc:HGNC:21101]"}, {"versioned_ensembl_gene_id":"ENSG00000282167.1","gene_symbol":"AC243629.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15826305,"end":15826945,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139292.12","gene_symbol":"LGR5","gene_name":"leucine rich repeat containing G protein-coupled receptor 5 [Source:HGNC Symbol;Acc:HGNC:4504]","synonyms":"HG38,GPR67,GPR49,FEX","biotype":"protein_coding","ncbi_id":"8549","summary":"The protein encoded by this gene is a leucine-rich repeat-containing receptor (LGR) and member of the G protein-coupled, 7-transmembrane receptor (GPCR) superfamily. The encoded protein is a receptor for R-spondins and is involved in the canonical Wnt signaling pathway. This protein plays a role in the formation and maintenance of adult intestinal stem cells during postembryonic development. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":71439770,"end":71586310,"strand":1,"description":"leucine rich repeat containing G protein-coupled receptor 5 [Source:HGNC Symbol;Acc:HGNC:4504]"}, {"versioned_ensembl_gene_id":"ENSG00000282287.1","gene_symbol":"AC243629.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15811828,"end":15818147,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259595.1","gene_symbol":"AC025043.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44402685,"end":44427144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276438.3","gene_symbol":"PPP2R3B","gene_name":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]","synonyms":"PR70,PR48,PPP2R3LY,PPP2R3L","biotype":"protein_coding","ncbi_id":"28227","summary":"Protein phosphatase 2 (formerly named type 2A) is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phosphatase 2 holoenzymes are heterotrimeric proteins composed of a structural subunit A, a catalytic subunit C, and a regulatory subunit B. The regulatory subunit is encoded by a diverse set of genes that have been grouped into the B/PR55, B'/PR61, and B''/PR72 families. These different regulatory subunits confer distinct enzymatic specificities and intracellular localizations to the holozenzyme. The product of this gene belongs to the B'' family. The B'' family has been further divided into subfamilies. The product of this gene belongs to the beta subfamily of regulatory subunit B''. [provided by RefSeq, Apr 2010]","start":336496,"end":389645,"strand":-1,"description":"protein phosphatase 2 regulatory subunit B''beta [Source:HGNC Symbol;Acc:HGNC:13417]"}, {"versioned_ensembl_gene_id":"ENSG00000136986.9","gene_symbol":"DERL1","gene_name":"derlin 1 [Source:HGNC Symbol;Acc:HGNC:28454]","synonyms":"FLJ13784,derlin-1,DER1,DER-1,PRO2577,MGC3067","biotype":"protein_coding","ncbi_id":"79139","summary":"The protein encoded by this gene is a member of the derlin family. Members of this family participate in the ER-associated degradation response and retrotranslocate misfolded or unfolded proteins from the ER lumen to the cytosol for proteasomal degradation. This protein recognizes substrate in the ER and works in a complex to retrotranslocate it across the ER membrane into the cytosol. This protein may select cystic fibrosis transmembrane conductance regulator protein (CFTR) for degradation as well as unfolded proteins in Alzheimer's disease. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]","start":123013164,"end":123042423,"strand":-1,"description":"derlin 1 [Source:HGNC Symbol;Acc:HGNC:28454]"}, {"versioned_ensembl_gene_id":"ENSG00000257267.3","gene_symbol":"ZNF271P","gene_name":"zinc finger protein 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:13065]","synonyms":"ZNFEB,ZNF271,HZF7","biotype":"transcribed_unitary_pseudogene","ncbi_id":"10778","summary":"Zinc finger proteins interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Apr 2004]","start":35290282,"end":35328390,"strand":1,"description":"zinc finger protein 271, pseudogene [Source:HGNC Symbol;Acc:HGNC:13065]"}, {"versioned_ensembl_gene_id":"ENSG00000253463.1","gene_symbol":"HMGB1P19","gene_name":"high mobility group box 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39101]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419979","summary":null,"start":123123106,"end":123123682,"strand":1,"description":"high mobility group box 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:39101]"}, {"versioned_ensembl_gene_id":"ENSG00000009780.15","gene_symbol":"FAM76A","gene_name":"family with sequence similarity 76 member A [Source:HGNC Symbol;Acc:HGNC:28530]","synonyms":"MGC34648","biotype":"protein_coding","ncbi_id":"199870","summary":null,"start":27725979,"end":27763122,"strand":1,"description":"family with sequence similarity 76 member A [Source:HGNC Symbol;Acc:HGNC:28530]"}, {"versioned_ensembl_gene_id":"ENSG00000168124.2","gene_symbol":"OR1F1","gene_name":"olfactory receptor family 1 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:8194]","synonyms":"OR1F8,OR1F7,OR1F6,OR1F5,OR1F4,OR1F13P,OR1F10,OR16-90,OR16-89,OR16-88,OR16-37,OR16-36,Olfmf,OR3-145,OR1F9","biotype":"protein_coding","ncbi_id":"4992","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3204247,"end":3205188,"strand":1,"description":"olfactory receptor family 1 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:8194]"}, {"versioned_ensembl_gene_id":"ENSG00000231344.1","gene_symbol":"AL020997.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27739091,"end":27739439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259425.5","gene_symbol":"AC011767.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22770523,"end":22776199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232952.1","gene_symbol":"AL512844.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105891739,"end":105893517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237897.2","gene_symbol":"AL512844.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":105890693,"end":105891430,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175265.17","gene_symbol":"GOLGA8A","gene_name":"golgin A8 family member A [Source:HGNC Symbol;Acc:HGNC:31972]","synonyms":"GOLGIN-67,GM88","biotype":"protein_coding","ncbi_id":"23015","summary":"The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked, flattened membrane sacs referred to as cisternae. Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The golgins constitute a family of proteins which are localized to the Golgi. This gene encodes a golgin which structurally resembles its family member GOLGA2, suggesting that they may share a similar function. There are many similar copies of this gene on chromosome 15. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":34379068,"end":34437466,"strand":-1,"description":"golgin A8 family member A [Source:HGNC Symbol;Acc:HGNC:31972]"}, {"versioned_ensembl_gene_id":"ENSG00000196998.17","gene_symbol":"WDR45","gene_name":"WD repeat domain 45 [Source:HGNC Symbol;Acc:HGNC:28912]","synonyms":"WIPI4,WDRX1,NBIA5,JM5","biotype":"protein_coding","ncbi_id":"11152","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene has a pseudogene at chromosome 4q31.3. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity and full-length nature of some variants have not been determined. [provided by RefSeq, Jul 2008]","start":49071470,"end":49101170,"strand":-1,"description":"WD repeat domain 45 [Source:HGNC Symbol;Acc:HGNC:28912]"}, {"versioned_ensembl_gene_id":"ENSG00000232360.1","gene_symbol":"AP000281.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32844367,"end":32849934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274973.1","gene_symbol":"BSNDP2","gene_name":"barttin CLCNK type accessory beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51537]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422517","summary":null,"start":25845497,"end":25845862,"strand":1,"description":"barttin CLCNK type accessory beta subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51537]"}, {"versioned_ensembl_gene_id":"ENSG00000256968.1","gene_symbol":"SNRPEP2","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20733]","synonyms":"SNRPEL1,bA390F4.4","biotype":"processed_pseudogene","ncbi_id":"414153","summary":null,"start":6748703,"end":6748981,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20733]"}, {"versioned_ensembl_gene_id":"ENSG00000251587.1","gene_symbol":"LDHAP1","gene_name":"lactate dehydrogenase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6536]","synonyms":"LDHAL1","biotype":"processed_pseudogene","ncbi_id":"3940","summary":null,"start":4894182,"end":4895173,"strand":-1,"description":"lactate dehydrogenase A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6536]"}, {"versioned_ensembl_gene_id":"ENSG00000205930.8","gene_symbol":"C21orf62-AS1","gene_name":"C21orf62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1290]","synonyms":"C21orf49","biotype":"antisense_RNA","ncbi_id":"54067","summary":null,"start":32772100,"end":32893735,"strand":1,"description":"C21orf62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1290]"}, {"versioned_ensembl_gene_id":"ENSG00000225179.1","gene_symbol":"LINC00457","gene_name":"long intergenic non-protein coding RNA 457 [Source:HGNC Symbol;Acc:HGNC:42805]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874179","summary":null,"start":34435450,"end":34640685,"strand":-1,"description":"long intergenic non-protein coding RNA 457 [Source:HGNC Symbol;Acc:HGNC:42805]"}, {"versioned_ensembl_gene_id":"ENSG00000278477.1","gene_symbol":"AL356321.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34262863,"end":34263090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272159.1","gene_symbol":"AC087623.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38408048,"end":38408742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241765.2","gene_symbol":"RPS26P45","gene_name":"ribosomal protein S26 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36944]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271570","summary":null,"start":69422656,"end":69422995,"strand":1,"description":"ribosomal protein S26 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:36944]"}, {"versioned_ensembl_gene_id":"ENSG00000188037.10","gene_symbol":"CLCN1","gene_name":"chloride voltage-gated channel 1 [Source:HGNC Symbol;Acc:HGNC:2019]","synonyms":"CLC1,ClC-1","biotype":"protein_coding","ncbi_id":"1180","summary":"The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":143316126,"end":143352083,"strand":1,"description":"chloride voltage-gated channel 1 [Source:HGNC Symbol;Acc:HGNC:2019]"}, {"versioned_ensembl_gene_id":"ENSG00000102898.11","gene_symbol":"NUTF2","gene_name":"nuclear transport factor 2 [Source:HGNC Symbol;Acc:HGNC:13722]","synonyms":"PP15,NTF2","biotype":"protein_coding","ncbi_id":"10204","summary":"This gene encodes a cytosolic factor that facilitates protein transport into the nucleus. The encoded protein is required for nuclear import of the small Ras-like GTPase, Ran which is involved in numerous cellular processes. This protein also interacts with the nuclear pore complex glycoprotein p62. [provided by RefSeq, Apr 2016]","start":67846732,"end":67872567,"strand":1,"description":"nuclear transport factor 2 [Source:HGNC Symbol;Acc:HGNC:13722]"}, {"versioned_ensembl_gene_id":"ENSG00000010539.11","gene_symbol":"ZNF200","gene_name":"zinc finger protein 200 [Source:HGNC Symbol;Acc:HGNC:12993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7752","summary":null,"start":3222325,"end":3236221,"strand":-1,"description":"zinc finger protein 200 [Source:HGNC Symbol;Acc:HGNC:12993]"}, {"versioned_ensembl_gene_id":"ENSG00000259702.2","gene_symbol":"AC024337.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96045341,"end":96064357,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196946.10","gene_symbol":"ZNF705A","gene_name":"zinc finger protein 705A [Source:HGNC Symbol;Acc:HGNC:32281]","synonyms":"FLJ16353","biotype":"protein_coding","ncbi_id":"440077","summary":null,"start":8157034,"end":8188537,"strand":1,"description":"zinc finger protein 705A [Source:HGNC Symbol;Acc:HGNC:32281]"}, {"versioned_ensembl_gene_id":"ENSG00000282345.1","gene_symbol":"FYTTD1P1","gene_name":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128665","summary":null,"start":101384932,"end":101386191,"strand":-1,"description":"forty-two-three domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38035]"}, {"versioned_ensembl_gene_id":"ENSG00000259763.1","gene_symbol":"LINC02157","gene_name":"long intergenic non-protein coding RNA 2157 [Source:HGNC Symbol;Acc:HGNC:53018]","synonyms":"RP11-327J17.1","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96235785,"end":96236703,"strand":1,"description":"long intergenic non-protein coding RNA 2157 [Source:HGNC Symbol;Acc:HGNC:53018]"}, {"versioned_ensembl_gene_id":"ENSG00000216307.2","gene_symbol":"AL136309.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4189116,"end":4189806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254090.1","gene_symbol":"MTND2P32","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873237","summary":null,"start":33015261,"end":33017043,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:42139]"}, {"versioned_ensembl_gene_id":"ENSG00000278865.1","gene_symbol":"AC012629.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10676096,"end":10676423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226443.3","gene_symbol":"GAPDHP32","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:37784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644213","summary":null,"start":119533749,"end":119534746,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:37784]"}, {"versioned_ensembl_gene_id":"ENSG00000124678.17","gene_symbol":"TCP11","gene_name":"t-complex 11 [Source:HGNC Symbol;Acc:HGNC:11658]","synonyms":"KIAA0229,FPPR,D6S230E","biotype":"protein_coding","ncbi_id":"6954","summary":null,"start":35118071,"end":35148610,"strand":-1,"description":"t-complex 11 [Source:HGNC Symbol;Acc:HGNC:11658]"}, {"versioned_ensembl_gene_id":"ENSG00000213211.2","gene_symbol":"KRT18P64","gene_name":"keratin 18 pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:48891]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107133513","summary":null,"start":85287789,"end":85289007,"strand":1,"description":"keratin 18 pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:48891]"}, {"versioned_ensembl_gene_id":"ENSG00000143870.12","gene_symbol":"PDIA6","gene_name":"protein disulfide isomerase family A member 6 [Source:HGNC Symbol;Acc:HGNC:30168]","synonyms":"TXNDC7,P5,ERp5","biotype":"protein_coding","ncbi_id":"10130","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, two catalytically active thioredoxin (TRX) domains, a TRX-like domain, and a C-terminal ER-retention sequence. This protein inhibits the aggregation of misfolded proteins and exhibits both isomerase and chaperone activity. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":10783391,"end":10837977,"strand":-1,"description":"protein disulfide isomerase family A member 6 [Source:HGNC Symbol;Acc:HGNC:30168]"}, {"versioned_ensembl_gene_id":"ENSG00000180347.13","gene_symbol":"CCDC129","gene_name":"coiled-coil domain containing 129 [Source:HGNC Symbol;Acc:HGNC:27363]","synonyms":"FLJ38344","biotype":"protein_coding","ncbi_id":"223075","summary":null,"start":31514071,"end":31658720,"strand":1,"description":"coiled-coil domain containing 129 [Source:HGNC Symbol;Acc:HGNC:27363]"}, {"versioned_ensembl_gene_id":"ENSG00000203857.9","gene_symbol":"HSD3B1","gene_name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 [Source:HGNC Symbol;Acc:HGNC:5217]","synonyms":"SDR11E1,HSDB3,HSD3B","biotype":"protein_coding","ncbi_id":"3283","summary":"The protein encoded by this gene is an enzyme that catalyzes the oxidative conversion of delta-5-3-beta-hydroxysteroid precursors into delta-4-ketosteroids, which leads to the production of all classes of steroid hormones. The encoded protein also catalyzes the interconversion of 3-beta-hydroxy- and 3-keto-5-alpha-androstane steroids. [provided by RefSeq, Jun 2016]","start":119507198,"end":119515054,"strand":1,"description":"hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 [Source:HGNC Symbol;Acc:HGNC:5217]"}, {"versioned_ensembl_gene_id":"ENSG00000179933.5","gene_symbol":"C14orf119","gene_name":"chromosome 14 open reading frame 119 [Source:HGNC Symbol;Acc:HGNC:20270]","synonyms":"FLJ20671","biotype":"protein_coding","ncbi_id":"55017","summary":null,"start":23094765,"end":23100462,"strand":1,"description":"chromosome 14 open reading frame 119 [Source:HGNC Symbol;Acc:HGNC:20270]"}, {"versioned_ensembl_gene_id":"ENSG00000141391.13","gene_symbol":"PRELID3A","gene_name":"PRELI domain containing 3A [Source:HGNC Symbol;Acc:HGNC:24639]","synonyms":"FLJ31484,C18orf43,SLMO1,HFL-EDDG1","biotype":"protein_coding","ncbi_id":"10650","summary":null,"start":12407896,"end":12432238,"strand":1,"description":"PRELI domain containing 3A [Source:HGNC Symbol;Acc:HGNC:24639]"}, {"versioned_ensembl_gene_id":"ENSG00000279458.2","gene_symbol":"AC244230.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46370759,"end":46382626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186971.3","gene_symbol":"KRTAP13-4","gene_name":"keratin associated protein 13-4 [Source:HGNC Symbol;Acc:HGNC:18926]","synonyms":"KAP13.4","biotype":"protein_coding","ncbi_id":"284827","summary":null,"start":30430230,"end":30431026,"strand":1,"description":"keratin associated protein 13-4 [Source:HGNC Symbol;Acc:HGNC:18926]"}, {"versioned_ensembl_gene_id":"ENSG00000225708.6","gene_symbol":"AL354984.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58069054,"end":58072070,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229233.1","gene_symbol":"AC011891.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":12654179,"end":12654985,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248690.6","gene_symbol":"HAS2-AS1","gene_name":"HAS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34340]","synonyms":"NCRNA00077,HASNT,HAS2AS,HAS2-AS","biotype":"antisense_RNA","ncbi_id":"594842","summary":null,"start":121639293,"end":121644693,"strand":1,"description":"HAS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:34340]"}, {"versioned_ensembl_gene_id":"ENSG00000249382.2","gene_symbol":"AC097501.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":58987182,"end":58988160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274273.1","gene_symbol":"ATP9B","gene_name":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]","synonyms":"ATPIIB","biotype":"protein_coding","ncbi_id":"374868","summary":null,"start":79074837,"end":79074964,"strand":1,"description":"ATPase phospholipid transporting 9B (putative) [Source:HGNC Symbol;Acc:HGNC:13541]"}, {"versioned_ensembl_gene_id":"ENSG00000245522.2","gene_symbol":"AC026250.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9754770,"end":9759533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244050.2","gene_symbol":"DEFB109F","gene_name":"defensin beta 109F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38066]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8199599,"end":8218911,"strand":-1,"description":"defensin beta 109F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38066]"}, {"versioned_ensembl_gene_id":"ENSG00000277865.4","gene_symbol":"GOLGA6L22","gene_name":"golgin A6 family-like 22 [Source:HGNC Symbol;Acc:HGNC:50289]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440243","summary":null,"start":22458903,"end":22469230,"strand":1,"description":"golgin A6 family-like 22 [Source:HGNC Symbol;Acc:HGNC:50289]"}, {"versioned_ensembl_gene_id":"ENSG00000226888.2","gene_symbol":"RPLP1P10","gene_name":"ribosomal protein lateral stalk subunit P1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35509]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271346","summary":null,"start":59088701,"end":59089039,"strand":-1,"description":"ribosomal protein lateral stalk subunit P1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35509]"}, {"versioned_ensembl_gene_id":"ENSG00000262280.1","gene_symbol":"LINC01896","gene_name":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]","synonyms":null,"biotype":"lincRNA","ncbi_id":"645321","summary":null,"start":78976555,"end":78979074,"strand":-1,"description":"long intergenic non-protein coding RNA 1896 [Source:HGNC Symbol;Acc:HGNC:52715]"}, {"versioned_ensembl_gene_id":"ENSG00000149634.4","gene_symbol":"SPATA25","gene_name":"spermatogenesis associated 25 [Source:HGNC Symbol;Acc:HGNC:16158]","synonyms":"TSG23,dJ337O18.8,C20orf165","biotype":"protein_coding","ncbi_id":"128497","summary":null,"start":45886489,"end":45887635,"strand":-1,"description":"spermatogenesis associated 25 [Source:HGNC Symbol;Acc:HGNC:16158]"}, {"versioned_ensembl_gene_id":"ENSG00000261462.1","gene_symbol":"AC004023.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87109539,"end":87111282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118972.1","gene_symbol":"FGF23","gene_name":"fibroblast growth factor 23 [Source:HGNC Symbol;Acc:HGNC:3680]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8074","summary":"This gene encodes a member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC). [provided by RefSeq, Feb 2013]","start":4368227,"end":4379728,"strand":-1,"description":"fibroblast growth factor 23 [Source:HGNC Symbol;Acc:HGNC:3680]"}, {"versioned_ensembl_gene_id":"ENSG00000206090.4","gene_symbol":"AP000350.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23939998,"end":23942798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260318.1","gene_symbol":"COX6CP1","gene_name":"cytochrome c oxidase subunit 6C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2286]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"9384","summary":null,"start":11903923,"end":11904137,"strand":-1,"description":"cytochrome c oxidase subunit 6C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2286]"}, {"versioned_ensembl_gene_id":"ENSG00000125462.16","gene_symbol":"C1orf61","gene_name":"chromosome 1 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:30780]","synonyms":"CROC4","biotype":"protein_coding","ncbi_id":"10485","summary":null,"start":156404250,"end":156430701,"strand":-1,"description":"chromosome 1 open reading frame 61 [Source:HGNC Symbol;Acc:HGNC:30780]"}, {"versioned_ensembl_gene_id":"ENSG00000278608.1","gene_symbol":"MAMDC2","gene_name":"MAM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23673]","synonyms":"MGC21981","biotype":"protein_coding","ncbi_id":"256691","summary":null,"start":70043581,"end":70176862,"strand":1,"description":"MAM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23673]"}, {"versioned_ensembl_gene_id":"ENSG00000254546.1","gene_symbol":"AC090099.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18196657,"end":18197337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255470.1","gene_symbol":"AC090099.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18140186,"end":18189495,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178445.9","gene_symbol":"GLDC","gene_name":"glycine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4313]","synonyms":"GCSP,NKH","biotype":"protein_coding","ncbi_id":"2731","summary":"Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).[provided by RefSeq, Jan 2010]","start":6532464,"end":6645783,"strand":-1,"description":"glycine decarboxylase [Source:HGNC Symbol;Acc:HGNC:4313]"}, {"versioned_ensembl_gene_id":"ENSG00000241570.8","gene_symbol":"PAQR9-AS1","gene_name":"PAQR9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50861]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927832","summary":null,"start":142960650,"end":143001559,"strand":1,"description":"PAQR9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50861]"}, {"versioned_ensembl_gene_id":"ENSG00000254857.1","gene_symbol":"AC090099.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18153277,"end":18154255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253168.1","gene_symbol":"AC124069.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17703988,"end":17706187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269968.1","gene_symbol":"AC006064.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6537794,"end":6538370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228405.5","gene_symbol":"RNF5","gene_name":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]","synonyms":"RMA1,NG2,G16,RING5","biotype":"protein_coding","ncbi_id":"6048","summary":"The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]","start":32126831,"end":32129264,"strand":1,"description":"ring finger protein 5 [Source:HGNC Symbol;Acc:HGNC:10068]"}, {"versioned_ensembl_gene_id":"ENSG00000144504.15","gene_symbol":"ANKMY1","gene_name":"ankyrin repeat and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20987]","synonyms":"ZMYND13,FLJ20499","biotype":"protein_coding","ncbi_id":"51281","summary":null,"start":240479422,"end":240569209,"strand":-1,"description":"ankyrin repeat and MYND domain containing 1 [Source:HGNC Symbol;Acc:HGNC:20987]"}, {"versioned_ensembl_gene_id":"ENSG00000234880.1","gene_symbol":"LINC00163","gene_name":"long intergenic non-protein coding RNA 163 [Source:HGNC Symbol;Acc:HGNC:33165]","synonyms":"NLC1A,NLC1-A,NCRNA00163,C21orf134","biotype":"lincRNA","ncbi_id":"727699","summary":null,"start":44989864,"end":44994086,"strand":-1,"description":"long intergenic non-protein coding RNA 163 [Source:HGNC Symbol;Acc:HGNC:33165]"}, {"versioned_ensembl_gene_id":"ENSG00000278017.1","gene_symbol":"AC064801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62525919,"end":62526325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262749.2","gene_symbol":"KRTAP9-3","gene_name":"keratin associated protein 9-3 [Source:HGNC Symbol;Acc:HGNC:16927]","synonyms":"KAP9.3","biotype":"protein_coding","ncbi_id":"83900","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41232462,"end":41233453,"strand":1,"description":"keratin associated protein 9-3 [Source:HGNC Symbol;Acc:HGNC:16927]"}, {"versioned_ensembl_gene_id":"ENSG00000282973.1","gene_symbol":"AC141257.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33345182,"end":33345396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138382.14","gene_symbol":"METTL5","gene_name":"methyltransferase like 5 [Source:HGNC Symbol;Acc:HGNC:25006]","synonyms":"HSPC133","biotype":"protein_coding","ncbi_id":"29081","summary":null,"start":169810081,"end":169824931,"strand":-1,"description":"methyltransferase like 5 [Source:HGNC Symbol;Acc:HGNC:25006]"}, {"versioned_ensembl_gene_id":"ENSG00000275034.2","gene_symbol":"TP53TG3E","gene_name":"TP53 target 3 family member E [Source:HGNC Symbol;Acc:HGNC:51816]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724101","summary":null,"start":33303739,"end":33306935,"strand":1,"description":"TP53 target 3 family member E [Source:HGNC Symbol;Acc:HGNC:51816]"}, {"versioned_ensembl_gene_id":"ENSG00000138303.17","gene_symbol":"ASCC1","gene_name":"activating signal cointegrator 1 complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24268]","synonyms":"Em:AC022392.3,CGI-18,ASC1p50","biotype":"protein_coding","ncbi_id":"51008","summary":"This gene encodes a subunit of the activating signal cointegrator 1 (ASC-1) complex. The ASC-1 complex is a transcriptional coactivator that plays an important role in gene transactivation by multiple transcription factors including activating protein 1 (AP-1), nuclear factor kappa-B (NF-kB) and serum response factor (SRF). The encoded protein contains an N-terminal KH-type RNA-binding motif which is required for AP-1 transactivation by the ASC-1 complex. Mutations in this gene are associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":72096032,"end":72217134,"strand":-1,"description":"activating signal cointegrator 1 complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24268]"}, {"versioned_ensembl_gene_id":"ENSG00000125885.13","gene_symbol":"MCM8","gene_name":"minichromosome maintenance 8 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:16147]","synonyms":"C20orf154,REC,MGC4816,MGC12866,MGC119523,MGC119522,dJ967N21.5","biotype":"protein_coding","ncbi_id":"84515","summary":"The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the mini-chromosome maintenance proteins is a key component of the pre-replication complex and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein contains the central domain that is conserved among the mini-chromosome maintenance proteins. The encoded protein may interact with other mini-chromosome maintenance proteins and play a role in DNA replication. This gene may be associated with length of reproductive lifespan and menopause. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013]","start":5950652,"end":5998977,"strand":1,"description":"minichromosome maintenance 8 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:16147]"}, {"versioned_ensembl_gene_id":"ENSG00000212978.6","gene_symbol":"AC016747.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":61141592,"end":61144969,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115297.10","gene_symbol":"TLX2","gene_name":"T-cell leukemia homeobox 2 [Source:HGNC Symbol;Acc:HGNC:5057]","synonyms":"Tlx2,NCX,HOX11L1,Enx","biotype":"protein_coding","ncbi_id":"3196","summary":"This gene is a member of an orphan homeobox-containing transcription factor family. Studies of the mouse ortholog have shown that the encoded protein is crucial for the development of the enteric nervous system; in humans, loss-of-function may play a role in tumorigenesis of gastrointestinal stromal tumors. [provided by RefSeq, May 2010]","start":74513463,"end":74517147,"strand":1,"description":"T-cell leukemia homeobox 2 [Source:HGNC Symbol;Acc:HGNC:5057]"}, {"versioned_ensembl_gene_id":"ENSG00000244060.2","gene_symbol":"AC003029.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111879338,"end":111880249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279789.1","gene_symbol":"AC120114.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":29913144,"end":29915337,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260114.2","gene_symbol":"AC120114.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29919634,"end":29921905,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234608.7","gene_symbol":"MAPKAPK5-AS1","gene_name":"MAPKAPK5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24091]","synonyms":"FLJ39616,C12orf47","biotype":"lincRNA","ncbi_id":"51275","summary":null,"start":111839764,"end":111842902,"strand":-1,"description":"MAPKAPK5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:24091]"}, {"versioned_ensembl_gene_id":"ENSG00000228285.2","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"dJ570F3.6,APT,LYPLA2L","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33365548,"end":33366243,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000143256.4","gene_symbol":"PFDN2","gene_name":"prefoldin subunit 2 [Source:HGNC Symbol;Acc:HGNC:8867]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5202","summary":"This gene encodes a member of the prefoldin beta subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The complex, consisting of two alpha and four beta subunits, forms a double beta barrel assembly with six protruding coiled-coils. [provided by RefSeq, Jul 2008]","start":161100556,"end":161118111,"strand":-1,"description":"prefoldin subunit 2 [Source:HGNC Symbol;Acc:HGNC:8867]"}, {"versioned_ensembl_gene_id":"ENSG00000235912.1","gene_symbol":"AL031729.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27649419,"end":27649610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112936.18","gene_symbol":"C7","gene_name":"complement C7 [Source:HGNC Symbol;Acc:HGNC:1346]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730","summary":"This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency. [provided by RefSeq, Nov 2016]","start":40909252,"end":40982939,"strand":1,"description":"complement C7 [Source:HGNC Symbol;Acc:HGNC:1346]"}, {"versioned_ensembl_gene_id":"ENSG00000254614.2","gene_symbol":"AP003068.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65177606,"end":65181834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109685.17","gene_symbol":"NSD2","gene_name":"nuclear receptor binding SET domain protein 2 [Source:HGNC Symbol;Acc:HGNC:12766]","synonyms":"WHSC1,MMSET,KMT3G","biotype":"protein_coding","ncbi_id":"7468","summary":"This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]","start":1871424,"end":1982207,"strand":1,"description":"nuclear receptor binding SET domain protein 2 [Source:HGNC Symbol;Acc:HGNC:12766]"}, {"versioned_ensembl_gene_id":"ENSG00000236453.5","gene_symbol":"AC003092.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94022833,"end":94066661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229160.1","gene_symbol":"AC009229.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38132637,"end":38138946,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268532.1","gene_symbol":"LINC02135","gene_name":"long intergenic non-protein coding RNA 2135 [Source:HGNC Symbol;Acc:HGNC:27094]","synonyms":null,"biotype":"lincRNA","ncbi_id":"146513","summary":null,"start":86286427,"end":86293389,"strand":1,"description":"long intergenic non-protein coding RNA 2135 [Source:HGNC Symbol;Acc:HGNC:27094]"}, {"versioned_ensembl_gene_id":"ENSG00000235848.4","gene_symbol":"RMDN2-AS1","gene_name":"RMDN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41150]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101410544","summary":null,"start":37949911,"end":38067041,"strand":-1,"description":"RMDN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41150]"}, {"versioned_ensembl_gene_id":"ENSG00000236938.1","gene_symbol":"AC003092.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94071759,"end":94077157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236068.2","gene_symbol":"AC091862.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":64404512,"end":64486615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275695.1","gene_symbol":"UBE2Q2P6","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49412]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421769","summary":null,"start":82445719,"end":82454837,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49412]"}, {"versioned_ensembl_gene_id":"ENSG00000238164.6","gene_symbol":"TNFRSF14-AS1","gene_name":"TNFRSF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26966]","synonyms":"ENST00000416860.2","biotype":"antisense_RNA","ncbi_id":"115110","summary":null,"start":2549920,"end":2557031,"strand":-1,"description":"TNFRSF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26966]"}, {"versioned_ensembl_gene_id":"ENSG00000258107.1","gene_symbol":"AL158058.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29390346,"end":29436412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158796.16","gene_symbol":"DEDD","gene_name":"death effector domain containing [Source:HGNC Symbol;Acc:HGNC:2755]","synonyms":"KE05,FLDED1,DEFT,DEDD1,CASP8IP1","biotype":"protein_coding","ncbi_id":"9191","summary":"This gene encodes a protein that contains a death effector domain (DED). DED is a protein-protein interaction domain shared by adaptors, regulators and executors of the programmed cell death pathway. Overexpression of this gene was shown to induce weak apoptosis. Upon stimulation, this protein was found to translocate from cytoplasm to nucleus and colocalize with UBTF, a basal factor required for RNA polymerase I transcription, in the nucleolus. At least three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":161120974,"end":161132688,"strand":-1,"description":"death effector domain containing [Source:HGNC Symbol;Acc:HGNC:2755]"}, {"versioned_ensembl_gene_id":"ENSG00000257764.2","gene_symbol":"AC020656.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":69353493,"end":69354225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273343.1","gene_symbol":"AC007663.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":20318119,"end":20318749,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128185.9","gene_symbol":"DGCR6L","gene_name":"DiGeorge syndrome critical region gene 6 like [Source:HGNC Symbol;Acc:HGNC:18551]","synonyms":"FLJ10666","biotype":"protein_coding","ncbi_id":"85359","summary":"This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome. [provided by RefSeq, Jul 2008]","start":20314276,"end":20320080,"strand":-1,"description":"DiGeorge syndrome critical region gene 6 like [Source:HGNC Symbol;Acc:HGNC:18551]"}, {"versioned_ensembl_gene_id":"ENSG00000158691.14","gene_symbol":"ZSCAN12","gene_name":"zinc finger and SCAN domain containing 12 [Source:HGNC Symbol;Acc:HGNC:13172]","synonyms":"ZNF96,ZNF305,ZNF29K1,ZFP96,KIAA0426,dJ29K1.2","biotype":"protein_coding","ncbi_id":"9753","summary":null,"start":28378955,"end":28399734,"strand":-1,"description":"zinc finger and SCAN domain containing 12 [Source:HGNC Symbol;Acc:HGNC:13172]"}, {"versioned_ensembl_gene_id":"ENSG00000168884.14","gene_symbol":"TNIP2","gene_name":"TNFAIP3 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:19118]","synonyms":"MGC4289,KLIP,FLIP1,ABIN-2","biotype":"protein_coding","ncbi_id":"79155","summary":"This gene encodes a protein which acts as an inhibitor of NFkappaB activation. The encoded protein is also involved in MAP/ERK signaling pathway in specific cell types. It may be involved in apoptosis of endothelial cells. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome.[provided by RefSeq, May 2014]","start":2741648,"end":2756376,"strand":-1,"description":"TNFAIP3 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:19118]"}, {"versioned_ensembl_gene_id":"ENSG00000106077.18","gene_symbol":"ABHD11","gene_name":"abhydrolase domain containing 11 [Source:HGNC Symbol;Acc:HGNC:16407]","synonyms":"WBSCR21,PP1226","biotype":"protein_coding","ncbi_id":"83451","summary":"This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]","start":73736094,"end":73738867,"strand":-1,"description":"abhydrolase domain containing 11 [Source:HGNC Symbol;Acc:HGNC:16407]"}, {"versioned_ensembl_gene_id":"ENSG00000115841.19","gene_symbol":"RMDN2","gene_name":"regulator of microtubule dynamics 2 [Source:HGNC Symbol;Acc:HGNC:26567]","synonyms":"RMD2,FLJ32954,FAM82A1,FAM82A","biotype":"protein_coding","ncbi_id":"151393","summary":null,"start":37923187,"end":38067142,"strand":1,"description":"regulator of microtubule dynamics 2 [Source:HGNC Symbol;Acc:HGNC:26567]"}, {"versioned_ensembl_gene_id":"ENSG00000269397.1","gene_symbol":"AC011503.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":23927788,"end":23929287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213967.10","gene_symbol":"ZNF726","gene_name":"zinc finger protein 726 [Source:HGNC Symbol;Acc:HGNC:32462]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730087","summary":null,"start":23914876,"end":23945159,"strand":1,"description":"zinc finger protein 726 [Source:HGNC Symbol;Acc:HGNC:32462]"}, {"versioned_ensembl_gene_id":"ENSG00000266989.1","gene_symbol":"FTLP5","gene_name":"ferritin light chain pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37953]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131661","summary":null,"start":3870991,"end":3872107,"strand":1,"description":"ferritin light chain pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37953]"}, {"versioned_ensembl_gene_id":"ENSG00000273923.1","gene_symbol":"AC104260.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95225326,"end":95225864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248441.6","gene_symbol":"LINC01197","gene_name":"long intergenic non-protein coding RNA 1197 [Source:HGNC Symbol;Acc:HGNC:49597]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400456","summary":null,"start":95209099,"end":95327129,"strand":-1,"description":"long intergenic non-protein coding RNA 1197 [Source:HGNC Symbol;Acc:HGNC:49597]"}, {"versioned_ensembl_gene_id":"ENSG00000266412.5","gene_symbol":"NCOA4","gene_name":"nuclear receptor coactivator 4 [Source:HGNC Symbol;Acc:HGNC:7671]","synonyms":"RFG,PTC3,ELE1,DKFZp762E1112,ARA70","biotype":"protein_coding","ncbi_id":"8031","summary":"This gene encodes an androgen receptor coactivator. The encoded protein interacts with the androgen receptor in a ligand-dependent manner to enhance its transcriptional activity. Chromosomal translocations between this gene and the ret tyrosine kinase gene, also located on chromosome 10, have been associated with papillary thyroid carcinoma. Alternatively spliced transcript variants have been described. Pseudogenes are present on chromosomes 4, 5, 10, and 14. [provided by RefSeq, Feb 2009]","start":46005088,"end":46030714,"strand":-1,"description":"nuclear receptor coactivator 4 [Source:HGNC Symbol;Acc:HGNC:7671]"}, {"versioned_ensembl_gene_id":"ENSG00000242423.2","gene_symbol":"RPL12P36","gene_name":"ribosomal protein L12 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36598]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271408","summary":null,"start":58825891,"end":58826368,"strand":1,"description":"ribosomal protein L12 pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:36598]"}, {"versioned_ensembl_gene_id":"ENSG00000260451.1","gene_symbol":"GEMIN8P2","gene_name":"gem nuclear organelle associated protein 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644600","summary":null,"start":58776540,"end":58777563,"strand":1,"description":"gem nuclear organelle associated protein 8 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37977]"}, {"versioned_ensembl_gene_id":"ENSG00000047457.13","gene_symbol":"CP","gene_name":"ceruloplasmin [Source:HGNC Symbol;Acc:HGNC:2295]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1356","summary":"The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]","start":149162410,"end":149222055,"strand":-1,"description":"ceruloplasmin [Source:HGNC Symbol;Acc:HGNC:2295]"}, {"versioned_ensembl_gene_id":"ENSG00000259981.1","gene_symbol":"AF096876.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30089717,"end":30097836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280304.1","gene_symbol":"AC104260.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":95280753,"end":95284249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206249.3","gene_symbol":"AL359555.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38288331,"end":38326536,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156282.4","gene_symbol":"CLDN17","gene_name":"claudin 17 [Source:HGNC Symbol;Acc:HGNC:2038]","synonyms":"MGC126554,MGC126552","biotype":"protein_coding","ncbi_id":"26285","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is intronless and is clustered with CLDN8 on chromosome 21q22.11. [provided by RefSeq, Jun 2010]","start":30165564,"end":30166756,"strand":-1,"description":"claudin 17 [Source:HGNC Symbol;Acc:HGNC:2038]"}, {"versioned_ensembl_gene_id":"ENSG00000255213.1","gene_symbol":"NPM1P35","gene_name":"nucleophosmin 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:45214]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129067","summary":null,"start":62330946,"end":62331813,"strand":1,"description":"nucleophosmin 1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:45214]"}, {"versioned_ensembl_gene_id":"ENSG00000272033.1","gene_symbol":"AL136984.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":167379108,"end":167381000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187987.9","gene_symbol":"ZSCAN23","gene_name":"zinc finger and SCAN domain containing 23 [Source:HGNC Symbol;Acc:HGNC:21193]","synonyms":"ZNF453,ZNF390,dJ29K1.3.1","biotype":"protein_coding","ncbi_id":"222696","summary":null,"start":28431930,"end":28443502,"strand":-1,"description":"zinc finger and SCAN domain containing 23 [Source:HGNC Symbol;Acc:HGNC:21193]"}, {"versioned_ensembl_gene_id":"ENSG00000214369.2","gene_symbol":"AC009967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169790093,"end":169790885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164619.8","gene_symbol":"BMPER","gene_name":"BMP binding endothelial regulator [Source:HGNC Symbol;Acc:HGNC:24154]","synonyms":"CRIM3,Cv2","biotype":"protein_coding","ncbi_id":"168667","summary":"This gene encodes a secreted protein that interacts with, and inhibits bone morphogenetic protein (BMP) function. It has been shown to inhibit BMP2- and BMP4-dependent osteoblast differentiation and BMP-dependent differentiation of the chondrogenic cells. Mutations in this gene are associated with a lethal skeletal disorder, diaphanospondylodysostosis. [provided by RefSeq, Dec 2011]","start":33904911,"end":34155872,"strand":1,"description":"BMP binding endothelial regulator [Source:HGNC Symbol;Acc:HGNC:24154]"}, {"versioned_ensembl_gene_id":"ENSG00000227342.1","gene_symbol":"LINC00307","gene_name":"long intergenic non-protein coding RNA 307 [Source:HGNC Symbol;Acc:HGNC:16727]","synonyms":"NCRNA00307,D21S2091E","biotype":"lincRNA","ncbi_id":"266919","summary":null,"start":30209151,"end":30211783,"strand":-1,"description":"long intergenic non-protein coding RNA 307 [Source:HGNC Symbol;Acc:HGNC:16727]"}, {"versioned_ensembl_gene_id":"ENSG00000257514.5","gene_symbol":"AC117505.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101646720,"end":101659970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143190.21","gene_symbol":"POU2F1","gene_name":"POU class 2 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9212]","synonyms":"OTF1,OCT1","biotype":"protein_coding","ncbi_id":"5451","summary":"The OCT1 transcription factor was among the first identified members of the POU transcription factor family (summarized by Sturm et al., 1993 [PubMed 8314572]). Members of this family contain the POU domain, a 160-amino acid region necessary for DNA binding to the octameric sequence ATGCAAAT.[supplied by OMIM, Jul 2010]","start":167220829,"end":167427345,"strand":1,"description":"POU class 2 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9212]"}, {"versioned_ensembl_gene_id":"ENSG00000132677.12","gene_symbol":"RHBG","gene_name":"Rh family B glycoprotein (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14572]","synonyms":"SLC42A2","biotype":"protein_coding","ncbi_id":"57127","summary":"This gene encodes one of two non-erythroid members of the Rhesus (Rh) protein family. Non-erythroid Rh protein family members are mainly expressed in the kidney and belong to the methylammonium-ammonium permease/ammonia transporters superfamily. All Rh family proteins are predicted to be transmembrane proteins with 12 membrane spanning domains and intracytoplasmic N- and C-termini. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":156369212,"end":156385219,"strand":1,"description":"Rh family B glycoprotein (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:14572]"}, {"versioned_ensembl_gene_id":"ENSG00000156284.5","gene_symbol":"CLDN8","gene_name":"claudin 8 [Source:HGNC Symbol;Acc:HGNC:2050]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9073","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This protein plays important roles in the paracellular cation barrier of the distal renal tubule, and in the paracellular barrier to prevent sodium back-leakage in distal colon. Differential expression of this gene has been observed in colorectal carcinoma and renal cell tumors, and along with claudin-7, is an immunohistochemical marker for the differential diagnosis of chromophobe renal cell carcinoma and renal oncocytoma.[provided by RefSeq, May 2010]","start":30214006,"end":30216073,"strand":-1,"description":"claudin 8 [Source:HGNC Symbol;Acc:HGNC:2050]"}, {"versioned_ensembl_gene_id":"ENSG00000269421.1","gene_symbol":"ZNF92P3","gene_name":"zinc finger protein 92 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39555]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419711","summary":null,"start":23935220,"end":23936173,"strand":1,"description":"zinc finger protein 92 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39555]"}, {"versioned_ensembl_gene_id":"ENSG00000269289.5","gene_symbol":"AC011503.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23919081,"end":23957930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233874.2","gene_symbol":"AL118496.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109568478,"end":109570289,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000005889.15","gene_symbol":"ZFX","gene_name":"zinc finger protein, X-linked [Source:HGNC Symbol;Acc:HGNC:12869]","synonyms":"ZNF926","biotype":"protein_coding","ncbi_id":"7543","summary":"This gene on the X chromosome is structurally similar to a related gene on the Y chromosome. It encodes a member of the krueppel C2H2-type zinc-finger protein family. The full-length protein contains an acidic transcriptional activation domain (AD), a nuclear localization sequence (NLS) and a DNA binding domain (DBD) consisting of 13 C2H2-type zinc fingers. Studies in mouse embryonic and adult hematopoietic stem cells showed that this gene was required as a transcriptional regulator for self-renewal of both stem cell types, but it was dispensable for growth and differentiation of their progeny. Multiple alternatively spliced transcript variants encoding different isoforms have been identified, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2010]","start":24149173,"end":24216255,"strand":1,"description":"zinc finger protein, X-linked [Source:HGNC Symbol;Acc:HGNC:12869]"}, {"versioned_ensembl_gene_id":"ENSG00000215005.2","gene_symbol":"HSPD1P7","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:5268]","synonyms":"HSPDP7,HSPD1-22P","biotype":"processed_pseudogene","ncbi_id":"54047","summary":null,"start":28887280,"end":28889272,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:5268]"}, {"versioned_ensembl_gene_id":"ENSG00000233131.1","gene_symbol":"AC096649.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175184215,"end":175184607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186479.4","gene_symbol":"RGS7BP","gene_name":"regulator of G protein signaling 7 binding protein [Source:HGNC Symbol;Acc:HGNC:23271]","synonyms":"R7BP","biotype":"protein_coding","ncbi_id":"401190","summary":"This gene encodes a protein that binds to all members of the R7 subfamily of regulators of G protein signaling and regulates their translocation between the nucleus and the plasma membrane. The encoded protein could be regulated by reversible palmitoylation, which anchors it to the plasma membrane. Depalmitoylation localizes the protein to the nucleus. Polymorphisms in this gene may be associated with risk of aspirin-exacerbated respiratory disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2012]","start":64506257,"end":64612312,"strand":1,"description":"regulator of G protein signaling 7 binding protein [Source:HGNC Symbol;Acc:HGNC:23271]"}, {"versioned_ensembl_gene_id":"ENSG00000255126.1","gene_symbol":"AP003064.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62391516,"end":62393372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154518.9","gene_symbol":"ATP5G3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:843]","synonyms":null,"biotype":"protein_coding","ncbi_id":"518","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding different proteins have been identified. [provided by RefSeq, Jun 2010]","start":175176258,"end":175184607,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:843]"}, {"versioned_ensembl_gene_id":"ENSG00000226309.1","gene_symbol":"SMARCE1P2","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39732]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442233","summary":null,"start":84429584,"end":84430802,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39732]"}, {"versioned_ensembl_gene_id":"ENSG00000101019.21","gene_symbol":"UQCC1","gene_name":"ubiquinol-cytochrome c reductase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:15891]","synonyms":"UQCC,FLJ10850,CBP3,C20orf44,BFZB","biotype":"protein_coding","ncbi_id":"55245","summary":"This gene encodes a transmembrane protein that is structurally similar to the mouse basic fibroblast growth factor repressed ZIC-binding protein. In mouse this protein may be involved in fibroblast growth factor regulated growth control. In humans, polymorphisms in this gene are associated with variation in human height and osteoarthritis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":35302566,"end":35412141,"strand":-1,"description":"ubiquinol-cytochrome c reductase complex assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:15891]"}, {"versioned_ensembl_gene_id":"ENSG00000254454.2","gene_symbol":"RCC2P6","gene_name":"regulator of chromosome condensation 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42382]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421131","summary":null,"start":62371146,"end":62373168,"strand":1,"description":"regulator of chromosome condensation 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42382]"}, {"versioned_ensembl_gene_id":"ENSG00000151461.19","gene_symbol":"UPF2","gene_name":"UPF2, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:17854]","synonyms":"smg-3,RENT2,KIAA1408,DKFZP434D222","biotype":"protein_coding","ncbi_id":"26019","summary":"This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein is located in the perinuclear area. It interacts with translation release factors and the proteins that are functional homologs of yeast Upf1p and Upf3p. Two splice variants have been found for this gene; both variants encode the same protein. [provided by RefSeq, Jul 2008]","start":11920022,"end":12043170,"strand":-1,"description":"UPF2, regulator of nonsense mediated mRNA decay [Source:HGNC Symbol;Acc:HGNC:17854]"}, {"versioned_ensembl_gene_id":"ENSG00000255118.1","gene_symbol":"AP003306.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62336911,"end":62338090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248120.1","gene_symbol":"AC114967.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40967505,"end":40967763,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162174.12","gene_symbol":"ASRGL1","gene_name":"asparaginase like 1 [Source:HGNC Symbol;Acc:HGNC:16448]","synonyms":"FLJ22316,ALP1,ALP","biotype":"protein_coding","ncbi_id":"80150","summary":null,"start":62337448,"end":62393412,"strand":1,"description":"asparaginase like 1 [Source:HGNC Symbol;Acc:HGNC:16448]"}, {"versioned_ensembl_gene_id":"ENSG00000249763.1","gene_symbol":"AC114786.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69242628,"end":69250815,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279617.1","gene_symbol":"AC005796.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17871273,"end":17871705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181101.7","gene_symbol":"SDCCAG3P2","gene_name":"serologically defined colon cancer antigen 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646891","summary":null,"start":175044626,"end":175045648,"strand":-1,"description":"serologically defined colon cancer antigen 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39164]"}, {"versioned_ensembl_gene_id":"ENSG00000226917.5","gene_symbol":"LINC01276","gene_name":"long intergenic non-protein coding RNA 1276 [Source:HGNC Symbol;Acc:HGNC:50333]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103106903","summary":null,"start":41502444,"end":41519852,"strand":1,"description":"long intergenic non-protein coding RNA 1276 [Source:HGNC Symbol;Acc:HGNC:50333]"}, {"versioned_ensembl_gene_id":"ENSG00000234753.5","gene_symbol":"FOXP4-AS1","gene_name":"FOXP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50332]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101060264","summary":null,"start":41494853,"end":41548621,"strand":-1,"description":"FOXP4 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50332]"}, {"versioned_ensembl_gene_id":"ENSG00000270356.1","gene_symbol":"IGHV1OR15-4","gene_name":"immunoglobulin heavy variable 1/OR15-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5566]","synonyms":"IGHV1/OR15-4","biotype":"IG_V_pseudogene","ncbi_id":"646379","summary":null,"start":22194885,"end":22195317,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5566]"}, {"versioned_ensembl_gene_id":"ENSG00000256862.1","gene_symbol":"AC005842.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3871734,"end":3910338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271507.1","gene_symbol":"AC025884.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22202392,"end":22202734,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259098.1","gene_symbol":"AC025884.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22258138,"end":22258848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111224.13","gene_symbol":"PARP11","gene_name":"poly(ADP-ribose) polymerase family member 11 [Source:HGNC Symbol;Acc:HGNC:1186]","synonyms":"C12orf6","biotype":"protein_coding","ncbi_id":"57097","summary":null,"start":3791047,"end":3873448,"strand":-1,"description":"poly(ADP-ribose) polymerase family member 11 [Source:HGNC Symbol;Acc:HGNC:1186]"}, {"versioned_ensembl_gene_id":"ENSG00000237319.1","gene_symbol":"AL118496.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":109636834,"end":109637063,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168367.9","gene_symbol":"LINC00917","gene_name":"long intergenic non-protein coding RNA 917 [Source:HGNC Symbol;Acc:HGNC:48607]","synonyms":null,"biotype":"lincRNA","ncbi_id":"732275","summary":null,"start":86331844,"end":86349683,"strand":-1,"description":"long intergenic non-protein coding RNA 917 [Source:HGNC Symbol;Acc:HGNC:48607]"}, {"versioned_ensembl_gene_id":"ENSG00000068366.19","gene_symbol":"ACSL4","gene_name":"acyl-CoA synthetase long chain family member 4 [Source:HGNC Symbol;Acc:HGNC:3571]","synonyms":"MRX68,MRX63,LACS4,FACL4,ACS4","biotype":"protein_coding","ncbi_id":"2182","summary":"The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016]","start":109624244,"end":109733403,"strand":-1,"description":"acyl-CoA synthetase long chain family member 4 [Source:HGNC Symbol;Acc:HGNC:3571]"}, {"versioned_ensembl_gene_id":"ENSG00000137166.14","gene_symbol":"FOXP4","gene_name":"forkhead box P4 [Source:HGNC Symbol;Acc:HGNC:20842]","synonyms":"FLJ40908","biotype":"protein_coding","ncbi_id":"116113","summary":"This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Many members of the forkhead box gene family, including members of subfamily P, have roles in mammalian oncogenesis. This gene may play a role in the development of tumors of the kidney and larynx. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms. [provided by RefSeq, Jul 2008]","start":41546426,"end":41602384,"strand":1,"description":"forkhead box P4 [Source:HGNC Symbol;Acc:HGNC:20842]"}, {"versioned_ensembl_gene_id":"ENSG00000197498.12","gene_symbol":"RPF2","gene_name":"ribosome production factor 2 homolog [Source:HGNC Symbol;Acc:HGNC:20870]","synonyms":"FLJ21087,BXDC1,bA397G5.4","biotype":"protein_coding","ncbi_id":"84154","summary":null,"start":110982015,"end":111028263,"strand":1,"description":"ribosome production factor 2 homolog [Source:HGNC Symbol;Acc:HGNC:20870]"}, {"versioned_ensembl_gene_id":"ENSG00000165192.13","gene_symbol":"ASB11","gene_name":"ankyrin repeat and SOCS box containing 11 [Source:HGNC Symbol;Acc:HGNC:17186]","synonyms":"DKFZp779E2460","biotype":"protein_coding","ncbi_id":"140456","summary":"The protein encoded by this gene is a member of the ankyrin repeat and SOCS box-containing (ASB) family of proteins. They contain ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, possibly targeting them for degradation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":15281697,"end":15315656,"strand":-1,"description":"ankyrin repeat and SOCS box containing 11 [Source:HGNC Symbol;Acc:HGNC:17186]"}, {"versioned_ensembl_gene_id":"ENSG00000274081.4","gene_symbol":"PUF60","gene_name":"poly(U) binding splicing factor 60 [Source:HGNC Symbol;Acc:HGNC:17042]","synonyms":"SIAHBP1,RoBPI,FIR","biotype":"protein_coding","ncbi_id":"22827","summary":"This gene encodes a nucleic acid-binding protein that plays a role in a variety of nuclear processes, including pre-mRNA splicing and transcriptional regulation. The encoded protein forms a complex with the far upstream DNA element (FUSE) and FUSE-binding protein at the myelocytomatosis oncogene (MYC) promoter. This complex represses MYC transcription through the core-TFIIH basal transcription factor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":143803351,"end":143816310,"strand":-1,"description":"poly(U) binding splicing factor 60 [Source:HGNC Symbol;Acc:HGNC:17042]"}, {"versioned_ensembl_gene_id":"ENSG00000095787.21","gene_symbol":"WAC","gene_name":"WW domain containing adaptor with coiled-coil [Source:HGNC Symbol;Acc:HGNC:17327]","synonyms":"PRO1741,MGC10753,FLJ31290,BM-016,Wwp4","biotype":"protein_coding","ncbi_id":"51322","summary":"The protein encoded by this gene contains a WW domain, which is a protein module found in a wide range of signaling proteins. This domain mediates protein-protein interactions and binds proteins containing short linear peptide motifs that are proline-rich or contain at least one proline. This gene product shares 94% sequence identity with the WAC protein in mouse, however, its exact function is not known. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]","start":28532493,"end":28623112,"strand":1,"description":"WW domain containing adaptor with coiled-coil [Source:HGNC Symbol;Acc:HGNC:17327]"}, {"versioned_ensembl_gene_id":"ENSG00000267285.1","gene_symbol":"AC004672.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1385833,"end":1386987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249028.2","gene_symbol":"AC004672.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1380060,"end":1391502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275811.1","gene_symbol":"HTR1DP1","gene_name":"5-hydroxytryptamine receptor 1D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5290]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421479","summary":null,"start":1151810,"end":1153059,"strand":-1,"description":"5-hydroxytryptamine receptor 1D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5290]"}, {"versioned_ensembl_gene_id":"ENSG00000225196.2","gene_symbol":"RPL10P17","gene_name":"ribosomal protein L10 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52348]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390998","summary":null,"start":12220794,"end":12221109,"strand":-1,"description":"ribosomal protein L10 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:52348]"}, {"versioned_ensembl_gene_id":"ENSG00000224074.3","gene_symbol":"LINC00691","gene_name":"long intergenic non-protein coding RNA 691 [Source:HGNC Symbol;Acc:HGNC:44514]","synonyms":null,"biotype":"lincRNA","ncbi_id":"152024","summary":null,"start":24096269,"end":24103238,"strand":-1,"description":"long intergenic non-protein coding RNA 691 [Source:HGNC Symbol;Acc:HGNC:44514]"}, {"versioned_ensembl_gene_id":"ENSG00000002016.17","gene_symbol":"RAD52","gene_name":"RAD52 homolog, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:9824]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5893","summary":"The protein encoded by this gene shares similarity with Saccharomyces cerevisiae Rad52, a protein important for DNA double-strand break repair and homologous recombination. This gene product was shown to bind single-stranded DNA ends, and mediate the DNA-DNA interaction necessary for the annealing of complementary DNA strands. It was also found to interact with DNA recombination protein RAD51, which suggested its role in RAD51 related DNA recombination and repair. A pseudogene of this gene is present on chromosome 2. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2014]","start":912077,"end":990053,"strand":-1,"description":"RAD52 homolog, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:9824]"}, {"versioned_ensembl_gene_id":"ENSG00000251460.1","gene_symbol":"AC097381.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8066528,"end":8067724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273267.1","gene_symbol":"AC097381.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8022665,"end":8023126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224418.1","gene_symbol":"STK24-AS1","gene_name":"STK24 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39935]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874069","summary":null,"start":98577244,"end":98578830,"strand":1,"description":"STK24 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39935]"}, {"versioned_ensembl_gene_id":"ENSG00000242109.1","gene_symbol":"NPM1P23","gene_name":"nucleophosmin 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:44513]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100422256","summary":null,"start":24096512,"end":24097360,"strand":-1,"description":"nucleophosmin 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:44513]"}, {"versioned_ensembl_gene_id":"ENSG00000158793.13","gene_symbol":"NIT1","gene_name":"nitrilase 1 [Source:HGNC Symbol;Acc:HGNC:7828]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4817","summary":"This gene encodes a member of the nitrilase protein family with homology to bacterial and plant nitrilases, enzymes that cleave nitriles and organic amides to the corresponding carboxylic acids plus ammonia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]","start":161118086,"end":161125445,"strand":1,"description":"nitrilase 1 [Source:HGNC Symbol;Acc:HGNC:7828]"}, {"versioned_ensembl_gene_id":"ENSG00000269599.1","gene_symbol":"AL161896.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":98329655,"end":98333236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236212.1","gene_symbol":"AC009262.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34209526,"end":34256343,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269189.1","gene_symbol":"AL445223.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":98233650,"end":98234700,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259225.6","gene_symbol":"LINC02345","gene_name":"long intergenic non-protein coding RNA 2345 [Source:HGNC Symbol;Acc:HGNC:53267]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928227","summary":null,"start":37984766,"end":38062340,"strand":1,"description":"long intergenic non-protein coding RNA 2345 [Source:HGNC Symbol;Acc:HGNC:53267]"}, {"versioned_ensembl_gene_id":"ENSG00000108474.16","gene_symbol":"PIGL","gene_name":"phosphatidylinositol glycan anchor biosynthesis class L [Source:HGNC Symbol;Acc:HGNC:8966]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9487","summary":"This gene encodes an enzyme that catalyzes the second step of glycosylphosphatidylinositol (GPI) biosynthesis, which is the de-N-acetylation of N-acetylglucosaminylphosphatidylinositol (GlcNAc-PI). Study of a similar rat enzyme suggests that this protein localizes to the endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":16217191,"end":16351797,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class L [Source:HGNC Symbol;Acc:HGNC:8966]"}, {"versioned_ensembl_gene_id":"ENSG00000152767.16","gene_symbol":"FARP1","gene_name":"FERM, ARH/RhoGEF and pleckstrin domain protein 1 [Source:HGNC Symbol;Acc:HGNC:3591]","synonyms":"PPP1R75,PLEKHC2,MGC87400,CDEP","biotype":"protein_coding","ncbi_id":"10160","summary":"This gene encodes a protein containing a FERM (4.2, exrin, radixin, moesin) domain, a Dbl homology domain, and two pleckstrin homology domains. These domains are found in guanine nucleotide exchange factors and proteins that link the cytoskeleton to the cell membrane. The encoded protein functions in neurons to promote dendritic growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":98142562,"end":98455176,"strand":1,"description":"FERM, ARH/RhoGEF and pleckstrin domain protein 1 [Source:HGNC Symbol;Acc:HGNC:3591]"}, {"versioned_ensembl_gene_id":"ENSG00000163995.19","gene_symbol":"ABLIM2","gene_name":"actin binding LIM protein family member 2 [Source:HGNC Symbol;Acc:HGNC:19195]","synonyms":"KIAA1808","biotype":"protein_coding","ncbi_id":"84448","summary":null,"start":7965310,"end":8158832,"strand":-1,"description":"actin binding LIM protein family member 2 [Source:HGNC Symbol;Acc:HGNC:19195]"}, {"versioned_ensembl_gene_id":"ENSG00000269826.1","gene_symbol":"AC092327.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86347387,"end":86349611,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225969.2","gene_symbol":"ABHD11-AS1","gene_name":"ABHD11 antisense RNA 1 (tail to tail) [Source:HGNC Symbol;Acc:HGNC:18289]","synonyms":"WBSCR26,NCRNA00035,LINC00035","biotype":"transcribed_unitary_pseudogene","ncbi_id":"171022","summary":null,"start":73735038,"end":73736158,"strand":1,"description":"ABHD11 antisense RNA 1 (tail to tail) [Source:HGNC Symbol;Acc:HGNC:18289]"}, {"versioned_ensembl_gene_id":"ENSG00000135226.17","gene_symbol":"UGT2B28","gene_name":"UDP glucuronosyltransferase family 2 member B28 [Source:HGNC Symbol;Acc:HGNC:13479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54490","summary":"This gene encodes a member of the uridine diphosphoglucuronosyltransferase protein family. The encoded enzyme catalyzes the transfer of glucuronic acid from uridine diphosphoglucuronic acid to a diverse array of substrates including steroid hormones and lipid-soluble drugs. This process, known as glucuronidation, is an intermediate step in the metabolism of steroids. Two transcript variants encoding different isoforms have been found for this gene. While both isoforms are targeted to the endoplasmic reticulum, only the longer isoform appears to be active. [provided by RefSeq, May 2011]","start":69280499,"end":69295050,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B28 [Source:HGNC Symbol;Acc:HGNC:13479]"}, {"versioned_ensembl_gene_id":"ENSG00000198671.3","gene_symbol":"AC135895.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65017468,"end":65054124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160256.12","gene_symbol":"FAM207A","gene_name":"family with sequence similarity 207 member A [Source:HGNC Symbol;Acc:HGNC:15811]","synonyms":"PRED56,C21orf70","biotype":"protein_coding","ncbi_id":"85395","summary":null,"start":44940010,"end":44976989,"strand":1,"description":"family with sequence similarity 207 member A [Source:HGNC Symbol;Acc:HGNC:15811]"}, {"versioned_ensembl_gene_id":"ENSG00000006788.13","gene_symbol":"MYH13","gene_name":"myosin heavy chain 13 [Source:HGNC Symbol;Acc:HGNC:7571]","synonyms":"MyHC-eo","biotype":"protein_coding","ncbi_id":"8735","summary":null,"start":10300865,"end":10373130,"strand":-1,"description":"myosin heavy chain 13 [Source:HGNC Symbol;Acc:HGNC:7571]"}, {"versioned_ensembl_gene_id":"ENSG00000264067.1","gene_symbol":"AC005291.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10320392,"end":10341458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267311.1","gene_symbol":"AC007673.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54879457,"end":54880809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156076.9","gene_symbol":"WIF1","gene_name":"WNT inhibitory factor 1 [Source:HGNC Symbol;Acc:HGNC:18081]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11197","summary":"The protein encoded by this gene functions to inhibit WNT proteins, which are extracellular signaling molecules that play a role in embryonic development. This protein contains a WNT inhibitory factor (WIF) domain and five epidermal growth factor (EGF)-like domains, and is thought to be involved in mesoderm segmentation. This gene functions as a tumor suppressor gene, and has been found to be epigenetically silenced in various cancers. [provided by RefSeq, Jun 2010]","start":65050626,"end":65121566,"strand":-1,"description":"WNT inhibitory factor 1 [Source:HGNC Symbol;Acc:HGNC:18081]"}, {"versioned_ensembl_gene_id":"ENSG00000248216.1","gene_symbol":"KCTD9P5","gene_name":"potassium channel tetramerization domain containing 9 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422179","summary":null,"start":37505688,"end":37506857,"strand":-1,"description":"potassium channel tetramerization domain containing 9 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49914]"}, {"versioned_ensembl_gene_id":"ENSG00000082068.8","gene_symbol":"WDR70","gene_name":"WD repeat domain 70 [Source:HGNC Symbol;Acc:HGNC:25495]","synonyms":"FLJ10233","biotype":"protein_coding","ncbi_id":"55100","summary":null,"start":37379212,"end":37753435,"strand":1,"description":"WD repeat domain 70 [Source:HGNC Symbol;Acc:HGNC:25495]"}, {"versioned_ensembl_gene_id":"ENSG00000224948.1","gene_symbol":"ATP5G1P8","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39511]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288222","summary":null,"start":76836568,"end":76836861,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C1 (subunit 9) pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39511]"}, {"versioned_ensembl_gene_id":"ENSG00000274271.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000119760.15","gene_symbol":"SUPT7L","gene_name":"SPT7 like, STAGA complex gamma subunit [Source:HGNC Symbol;Acc:HGNC:30632]","synonyms":"STAF65gamma,STAF65,SPT7L,KIAA0764","biotype":"protein_coding","ncbi_id":"9913","summary":"SUPT7L is a protein subunit of the human STAGA complex (SPT3; (MIM 602947)/TAF9 (MIM 600822)/GCN5 (MIM 602301) acetyltransferase complex), which is a chromatin-modifying multiprotein complex (Martinez et al., 2001 [PubMed 11564863]).[supplied by OMIM, Apr 2009]","start":27650812,"end":27663840,"strand":-1,"description":"SPT7 like, STAGA complex gamma subunit [Source:HGNC Symbol;Acc:HGNC:30632]"}, {"versioned_ensembl_gene_id":"ENSG00000118976.5","gene_symbol":"OTUD4P1","gene_name":"OTUD4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33912]","synonyms":"HIN1L","biotype":"processed_pseudogene","ncbi_id":"360227","summary":null,"start":3839459,"end":3842525,"strand":1,"description":"OTUD4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33912]"}, {"versioned_ensembl_gene_id":"ENSG00000215317.2","gene_symbol":"THUMPD1P1","gene_name":"THUMP domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23808]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391276","summary":null,"start":28901779,"end":28903697,"strand":-1,"description":"THUMP domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23808]"}, {"versioned_ensembl_gene_id":"ENSG00000211676.2","gene_symbol":"IGLJ2","gene_name":"immunoglobulin lambda joining 2 [Source:HGNC Symbol;Acc:HGNC:5864]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28832","summary":null,"start":22899481,"end":22899655,"strand":1,"description":"immunoglobulin lambda joining 2 [Source:HGNC Symbol;Acc:HGNC:5864]"}, {"versioned_ensembl_gene_id":"ENSG00000227129.6","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31934136,"end":31939383,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000234230.1","gene_symbol":"ZFX-AS1","gene_name":"ZFX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40617]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873922","summary":null,"start":24146225,"end":24149654,"strand":-1,"description":"ZFX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40617]"}, {"versioned_ensembl_gene_id":"ENSG00000182405.5","gene_symbol":"PGBD4","gene_name":"piggyBac transposable element derived 4 [Source:HGNC Symbol;Acc:HGNC:19401]","synonyms":"FLJ37497,FLJ32638","biotype":"protein_coding","ncbi_id":"161779","summary":"The piggyBac family of proteins, found in diverse animals, are transposases related to the transposase of the canonical piggyBac transposon from the moth, Trichoplusia ni. This family also includes genes in several genomes, including human, that appear to have been derived from the piggyBac transposons. This gene belongs to the subfamily of piggyBac transposable element derived (PGBD) genes. The PGBD proteins appear to be novel, with no obvious relationship to other transposases, or other known protein families. [provided by RefSeq, Jul 2008]","start":34102073,"end":34108684,"strand":1,"description":"piggyBac transposable element derived 4 [Source:HGNC Symbol;Acc:HGNC:19401]"}, {"versioned_ensembl_gene_id":"ENSG00000273139.1","gene_symbol":"AC007663.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20320739,"end":20321203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268129.1","gene_symbol":"AC026304.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143000907,"end":143001467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168122.4","gene_symbol":"ZNF355P","gene_name":"zinc finger protein 355, pseudogene [Source:HGNC Symbol;Acc:HGNC:17218]","synonyms":"ZNF834,PRED65","biotype":"unprocessed_pseudogene","ncbi_id":"100505852","summary":null,"start":13095305,"end":13113790,"strand":-1,"description":"zinc finger protein 355, pseudogene [Source:HGNC Symbol;Acc:HGNC:17218]"}, {"versioned_ensembl_gene_id":"ENSG00000211677.2","gene_symbol":"IGLC2","gene_name":"immunoglobulin lambda constant 2 [Source:HGNC Symbol;Acc:HGNC:5856]","synonyms":"IGLC","biotype":"IG_C_gene","ncbi_id":"3538","summary":null,"start":22900976,"end":22901437,"strand":1,"description":"immunoglobulin lambda constant 2 [Source:HGNC Symbol;Acc:HGNC:5856]"}, {"versioned_ensembl_gene_id":"ENSG00000163714.17","gene_symbol":"U2SURP","gene_name":"U2 snRNP associated SURP domain containing [Source:HGNC Symbol;Acc:HGNC:30855]","synonyms":"SR140,fSAPa","biotype":"protein_coding","ncbi_id":"23350","summary":null,"start":142964497,"end":143060546,"strand":1,"description":"U2 snRNP associated SURP domain containing [Source:HGNC Symbol;Acc:HGNC:30855]"}, {"versioned_ensembl_gene_id":"ENSG00000233633.1","gene_symbol":"AC093326.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":558204,"end":578145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211678.2","gene_symbol":"IGLJ3","gene_name":"immunoglobulin lambda joining 3 [Source:HGNC Symbol;Acc:HGNC:5865]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28831","summary":null,"start":22904850,"end":22905025,"strand":1,"description":"immunoglobulin lambda joining 3 [Source:HGNC Symbol;Acc:HGNC:5865]"}, {"versioned_ensembl_gene_id":"ENSG00000211679.2","gene_symbol":"IGLC3","gene_name":"immunoglobulin lambda constant 3 (Kern-Oz+ marker) [Source:HGNC Symbol;Acc:HGNC:5857]","synonyms":"IGLC","biotype":"IG_C_gene","ncbi_id":"3539","summary":null,"start":22906342,"end":22906803,"strand":1,"description":"immunoglobulin lambda constant 3 (Kern-Oz+ marker) [Source:HGNC Symbol;Acc:HGNC:5857]"}, {"versioned_ensembl_gene_id":"ENSG00000211680.2","gene_symbol":"IGLJ4","gene_name":"immunoglobulin lambda joining 4 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5866]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28830","summary":null,"start":22910574,"end":22910606,"strand":1,"description":"immunoglobulin lambda joining 4 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5866]"}, {"versioned_ensembl_gene_id":"ENSG00000254029.1","gene_symbol":"IGLC4","gene_name":"immunoglobulin lambda constant 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5858]","synonyms":"IGLC","biotype":"IG_C_pseudogene","ncbi_id":"3540","summary":null,"start":22910828,"end":22911075,"strand":1,"description":"immunoglobulin lambda constant 4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5858]"}, {"versioned_ensembl_gene_id":"ENSG00000235379.1","gene_symbol":"RPL7P31","gene_name":"ribosomal protein L7 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:36988]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270909","summary":null,"start":34710757,"end":34711480,"strand":1,"description":"ribosomal protein L7 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:36988]"}, {"versioned_ensembl_gene_id":"ENSG00000231535.5","gene_symbol":"LINC00278","gene_name":"long intergenic non-protein coding RNA 278 [Source:HGNC Symbol;Acc:HGNC:38712]","synonyms":"NCRNA00278","biotype":"lincRNA","ncbi_id":"100873962","summary":null,"start":3002912,"end":3102272,"strand":1,"description":"long intergenic non-protein coding RNA 278 [Source:HGNC Symbol;Acc:HGNC:38712]"}, {"versioned_ensembl_gene_id":"ENSG00000211681.2","gene_symbol":"IGLJ5","gene_name":"immunoglobulin lambda joining 5 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5867]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28829","summary":null,"start":22914237,"end":22914308,"strand":1,"description":"immunoglobulin lambda joining 5 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5867]"}, {"versioned_ensembl_gene_id":"ENSG00000254030.1","gene_symbol":"IGLC5","gene_name":"immunoglobulin lambda constant 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5859]","synonyms":"IGLC","biotype":"IG_C_pseudogene","ncbi_id":"3541","summary":null,"start":22915635,"end":22915927,"strand":1,"description":"immunoglobulin lambda constant 5 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5859]"}, {"versioned_ensembl_gene_id":"ENSG00000105641.3","gene_symbol":"SLC5A5","gene_name":"solute carrier family 5 member 5 [Source:HGNC Symbol;Acc:HGNC:11040]","synonyms":"NIS","biotype":"protein_coding","ncbi_id":"6528","summary":"This gene encodes a member of the sodium glucose cotransporter family. The encoded protein is responsible for the uptake of iodine in tissues such as the thyroid and lactating breast tissue. The iodine taken up by the thyroid is incorporated into the metabolic regulators triiodothyronine (T3) and tetraiodothyronine (T4). Mutations in this gene are associated with thyroid dyshormonogenesis 1.[provided by RefSeq, Sep 2009]","start":17871973,"end":17895174,"strand":1,"description":"solute carrier family 5 member 5 [Source:HGNC Symbol;Acc:HGNC:11040]"}, {"versioned_ensembl_gene_id":"ENSG00000233975.1","gene_symbol":"AL445490.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27660328,"end":27662722,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211682.2","gene_symbol":"IGLJ6","gene_name":"immunoglobulin lambda joining 6 [Source:HGNC Symbol;Acc:HGNC:5868]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28828","summary":null,"start":22918132,"end":22918201,"strand":1,"description":"immunoglobulin lambda joining 6 [Source:HGNC Symbol;Acc:HGNC:5868]"}, {"versioned_ensembl_gene_id":"ENSG00000222037.5","gene_symbol":"IGLC6","gene_name":"immunoglobulin lambda constant 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5860]","synonyms":"IGLC","biotype":"IG_C_pseudogene","ncbi_id":"3542","summary":null,"start":22919535,"end":22919851,"strand":1,"description":"immunoglobulin lambda constant 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5860]"}, {"versioned_ensembl_gene_id":"ENSG00000187258.13","gene_symbol":"NPSR1","gene_name":"neuropeptide S receptor 1 [Source:HGNC Symbol;Acc:HGNC:23631]","synonyms":"PGR14,GPRA,GPR154","biotype":"protein_coding","ncbi_id":"387129","summary":"This gene encodes a member of the vasopressin/oxytocin subfamily of G protein-coupled receptors. The encoded membrane protein acts as a receptor for neuropeptide S and affects a variety of cellular processes through its signaling. Increased expression of this gene in ciliated cells of the respiratory epithelium and in bronchial smooth muscle cells is associated with asthma. Polymorphisms in this gene have also been associated with asthma susceptibility, panic disorders, inflammatory bowel disease, and rheumatoid arthritis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":34658239,"end":34878332,"strand":1,"description":"neuropeptide S receptor 1 [Source:HGNC Symbol;Acc:HGNC:23631]"}, {"versioned_ensembl_gene_id":"ENSG00000258732.1","gene_symbol":"AC025884.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22278971,"end":22282872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240086.5","gene_symbol":"AC128689.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":135356067,"end":135439888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211684.2","gene_symbol":"IGLJ7","gene_name":"immunoglobulin lambda joining 7 [Source:HGNC Symbol;Acc:HGNC:5869]","synonyms":null,"biotype":"IG_J_gene","ncbi_id":"28827","summary":null,"start":22921390,"end":22921435,"strand":1,"description":"immunoglobulin lambda joining 7 [Source:HGNC Symbol;Acc:HGNC:5869]"}, {"versioned_ensembl_gene_id":"ENSG00000274835.1","gene_symbol":"AC100757.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22360639,"end":22360918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211685.3","gene_symbol":"IGLC7","gene_name":"immunoglobulin lambda constant 7 [Source:HGNC Symbol;Acc:HGNC:5861]","synonyms":null,"biotype":"IG_C_gene","ncbi_id":"28834","summary":null,"start":22922594,"end":22923034,"strand":1,"description":"immunoglobulin lambda constant 7 [Source:HGNC Symbol;Acc:HGNC:5861]"}, {"versioned_ensembl_gene_id":"ENSG00000161133.16","gene_symbol":"USP41","gene_name":"ubiquitin specific peptidase 41 [Source:HGNC Symbol;Acc:HGNC:20070]","synonyms":null,"biotype":"protein_coding","ncbi_id":"373856","summary":null,"start":20350578,"end":20390758,"strand":-1,"description":"ubiquitin specific peptidase 41 [Source:HGNC Symbol;Acc:HGNC:20070]"}, {"versioned_ensembl_gene_id":"ENSG00000232943.1","gene_symbol":"AL050321.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18220113,"end":18220512,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256969.1","gene_symbol":"AC007207.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4020977,"end":4026658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234652.1","gene_symbol":"AGPAT5P1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37709]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646231","summary":null,"start":3293808,"end":3294826,"strand":1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37709]"}, {"versioned_ensembl_gene_id":"ENSG00000237472.1","gene_symbol":"AC245054.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22988263,"end":22988581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223679.1","gene_symbol":"AC245054.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22990690,"end":23008356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256356.1","gene_symbol":"HSPA8P5","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399988","summary":null,"start":4097451,"end":4099519,"strand":1,"description":"heat shock protein family A (Hsp70) member 8 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44920]"}, {"versioned_ensembl_gene_id":"ENSG00000141664.9","gene_symbol":"ZCCHC2","gene_name":"zinc finger CCHC-type containing 2 [Source:HGNC Symbol;Acc:HGNC:22916]","synonyms":"KIAA1744,FLJ20281,FLJ20222,C18orf49","biotype":"protein_coding","ncbi_id":"54877","summary":null,"start":62523007,"end":62587709,"strand":1,"description":"zinc finger CCHC-type containing 2 [Source:HGNC Symbol;Acc:HGNC:22916]"}, {"versioned_ensembl_gene_id":"ENSG00000138061.11","gene_symbol":"CYP1B1","gene_name":"cytochrome P450 family 1 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2597]","synonyms":"GLC3A,CP1B","biotype":"protein_coding","ncbi_id":"1545","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The enzyme encoded by this gene localizes to the endoplasmic reticulum and metabolizes procarcinogens such as polycyclic aromatic hydrocarbons and 17beta-estradiol. Mutations in this gene have been associated with primary congenital glaucoma; therefore it is thought that the enzyme also metabolizes a signaling molecule involved in eye development, possibly a steroid. [provided by RefSeq, Jul 2008]","start":38066973,"end":38109902,"strand":-1,"description":"cytochrome P450 family 1 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2597]"}, {"versioned_ensembl_gene_id":"ENSG00000263826.1","gene_symbol":"AC112907.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186781780,"end":186784179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235578.1","gene_symbol":"AC007731.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20343203,"end":20344365,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134152.10","gene_symbol":"KATNBL1","gene_name":"katanin regulatory subunit B1 like 1 [Source:HGNC Symbol;Acc:HGNC:26199]","synonyms":"FLJ22557,C15orf29","biotype":"protein_coding","ncbi_id":"79768","summary":null,"start":34140674,"end":34210096,"strand":-1,"description":"katanin regulatory subunit B1 like 1 [Source:HGNC Symbol;Acc:HGNC:26199]"}, {"versioned_ensembl_gene_id":"ENSG00000156976.16","gene_symbol":"EIF4A2","gene_name":"eukaryotic translation initiation factor 4A2 [Source:HGNC Symbol;Acc:HGNC:3284]","synonyms":"BM-010,EIF4F,EIF4A,DDX2B","biotype":"protein_coding","ncbi_id":"1974","summary":null,"start":186783205,"end":186789900,"strand":1,"description":"eukaryotic translation initiation factor 4A2 [Source:HGNC Symbol;Acc:HGNC:3284]"}, {"versioned_ensembl_gene_id":"ENSG00000188280.11","gene_symbol":"AC007731.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20338805,"end":20354372,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259080.1","gene_symbol":"AC074091.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":27583046,"end":27635174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241889.1","gene_symbol":"AC079944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113885298,"end":113886031,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188542.9","gene_symbol":"DUSP28","gene_name":"dual specificity phosphatase 28 [Source:HGNC Symbol;Acc:HGNC:33237]","synonyms":"VHP,DUSP26","biotype":"protein_coding","ncbi_id":"285193","summary":null,"start":240560054,"end":240564014,"strand":1,"description":"dual specificity phosphatase 28 [Source:HGNC Symbol;Acc:HGNC:33237]"}, {"versioned_ensembl_gene_id":"ENSG00000240375.1","gene_symbol":"VPS26AP1","gene_name":"VPS26A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44611]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421731","summary":null,"start":113919222,"end":113920200,"strand":1,"description":"VPS26A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44611]"}, {"versioned_ensembl_gene_id":"ENSG00000227782.2","gene_symbol":"AC002553.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16040472,"end":16041273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243943.9","gene_symbol":"ZNF512","gene_name":"zinc finger protein 512 [Source:HGNC Symbol;Acc:HGNC:29380]","synonyms":"KIAA1805","biotype":"protein_coding","ncbi_id":"84450","summary":"This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012]","start":27582969,"end":27623215,"strand":1,"description":"zinc finger protein 512 [Source:HGNC Symbol;Acc:HGNC:29380]"}, {"versioned_ensembl_gene_id":"ENSG00000178075.19","gene_symbol":"GRAMD1C","gene_name":"GRAM domain containing 1C [Source:HGNC Symbol;Acc:HGNC:25252]","synonyms":"DKFZp434C0328","biotype":"protein_coding","ncbi_id":"54762","summary":null,"start":113828182,"end":113947174,"strand":1,"description":"GRAM domain containing 1C [Source:HGNC Symbol;Acc:HGNC:25252]"}, {"versioned_ensembl_gene_id":"ENSG00000271889.1","gene_symbol":"AC016747.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61151433,"end":61162105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258997.1","gene_symbol":"NF1P2","gene_name":"neurofibromin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38664]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"440225","summary":null,"start":21927657,"end":21946641,"strand":-1,"description":"neurofibromin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38664]"}, {"versioned_ensembl_gene_id":"ENSG00000254248.1","gene_symbol":"AC068189.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95071732,"end":95087924,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165819.11","gene_symbol":"METTL3","gene_name":"methyltransferase like 3 [Source:HGNC Symbol;Acc:HGNC:17563]","synonyms":"Spo8,MT-A70,M6A","biotype":"protein_coding","ncbi_id":"56339","summary":"This gene encodes the 70 kDa subunit of MT-A which is part of N6-adenosine-methyltransferase. This enzyme is involved in the posttranscriptional methylation of internal adenosine residues in eukaryotic mRNAs, forming N6-methyladenosine. [provided by RefSeq, Jul 2008]","start":21498133,"end":21511375,"strand":-1,"description":"methyltransferase like 3 [Source:HGNC Symbol;Acc:HGNC:17563]"}, {"versioned_ensembl_gene_id":"ENSG00000163283.6","gene_symbol":"ALPP","gene_name":"alkaline phosphatase, placental [Source:HGNC Symbol;Acc:HGNC:439]","synonyms":null,"biotype":"protein_coding","ncbi_id":"250","summary":"The protein encoded by this gene is an alkaline phosphatase, a metalloenzyme that catalyzes the hydrolysis of phosphoric acid monoesters. It belongs to a multigene family composed of four alkaline phosphatase isoenzymes. The enzyme functions as a homodimer and has a catalytic site containing one magnesium and two zinc ions, which are required for its enzymatic function. One of the main sources of this enzyme is the liver, and thus, it's one of several indicators of liver injury in different clinical conditions. In pregnant women, this protein is primarily expressed in placental and endometrial tissue, however, strong ectopic expression has been detected in ovarian adenocarcinoma, serous cystadenocarcinoma, and other ovarian cancer cells. [provided by RefSeq, Aug 2020]","start":232378534,"end":232382889,"strand":1,"description":"alkaline phosphatase, placental [Source:HGNC Symbol;Acc:HGNC:439]"}, {"versioned_ensembl_gene_id":"ENSG00000224516.5","gene_symbol":"AC068134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":232379635,"end":232381674,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233979.1","gene_symbol":"AC002553.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16084042,"end":16084381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214941.7","gene_symbol":"ZSWIM7","gene_name":"zinc finger SWIM-type containing 7 [Source:HGNC Symbol;Acc:HGNC:26993]","synonyms":"SWS1","biotype":"protein_coding","ncbi_id":"125150","summary":null,"start":15976560,"end":15999717,"strand":-1,"description":"zinc finger SWIM-type containing 7 [Source:HGNC Symbol;Acc:HGNC:26993]"}, {"versioned_ensembl_gene_id":"ENSG00000232818.2","gene_symbol":"RPS2P32","gene_name":"ribosomal protein S2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:30518]","synonyms":"MGC27348","biotype":"processed_pseudogene","ncbi_id":"256355","summary":null,"start":23490473,"end":23491364,"strand":1,"description":"ribosomal protein S2 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:30518]"}, {"versioned_ensembl_gene_id":"ENSG00000161132.6","gene_symbol":"AC007663.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20299760,"end":20313216,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229306.1","gene_symbol":"AP001464.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12999676,"end":13016692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257680.1","gene_symbol":"AC016144.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40728811,"end":40729897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274682.1","gene_symbol":"AC015540.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40978744,"end":40979244,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196793.13","gene_symbol":"ZNF239","gene_name":"zinc finger protein 239 [Source:HGNC Symbol;Acc:HGNC:13031]","synonyms":"MOK2,HOK-2","biotype":"protein_coding","ncbi_id":"8187","summary":"MOK2 proteins are DNA- and RNA-binding proteins that are mainly associated with nuclear RNP components, including the nucleoli and extranucleolar structures (Arranz et al., 1997 [PubMed 9121460]).[supplied by OMIM, Mar 2008]","start":43556344,"end":43574618,"strand":-1,"description":"zinc finger protein 239 [Source:HGNC Symbol;Acc:HGNC:13031]"}, {"versioned_ensembl_gene_id":"ENSG00000259800.1","gene_symbol":"AC145350.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33130235,"end":33130442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236499.2","gene_symbol":"LINC00896","gene_name":"long intergenic non-protein coding RNA 896 [Source:HGNC Symbol;Acc:HGNC:26519]","synonyms":"FLJ32575","biotype":"lincRNA","ncbi_id":"150197","summary":null,"start":20206397,"end":20208524,"strand":1,"description":"long intergenic non-protein coding RNA 896 [Source:HGNC Symbol;Acc:HGNC:26519]"}, {"versioned_ensembl_gene_id":"ENSG00000267062.1","gene_symbol":"AC018761.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12796823,"end":12801849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225998.6","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"G7b,C6orf28,YBL026W","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31873692,"end":31883281,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000253899.1","gene_symbol":"AC067904.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27063996,"end":27065278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236494.1","gene_symbol":"AC008080.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33793168,"end":33803156,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211672.2","gene_symbol":"IGLV4-3","gene_name":"immunoglobulin lambda variable 4-3 [Source:HGNC Symbol;Acc:HGNC:5919]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28786","summary":null,"start":22871507,"end":22872035,"strand":1,"description":"immunoglobulin lambda variable 4-3 [Source:HGNC Symbol;Acc:HGNC:5919]"}, {"versioned_ensembl_gene_id":"ENSG00000250290.1","gene_symbol":"NCAPGP1","gene_name":"non-SMC condensin I complex subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421096","summary":null,"start":120635558,"end":120638204,"strand":-1,"description":"non-SMC condensin I complex subunit G pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51904]"}, {"versioned_ensembl_gene_id":"ENSG00000014216.15","gene_symbol":"CAPN1","gene_name":"calpain 1 [Source:HGNC Symbol;Acc:HGNC:1476]","synonyms":"CANP,muCL,muCANP,CANPL1","biotype":"protein_coding","ncbi_id":"823","summary":"The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":65180566,"end":65212006,"strand":1,"description":"calpain 1 [Source:HGNC Symbol;Acc:HGNC:1476]"}, {"versioned_ensembl_gene_id":"ENSG00000197705.9","gene_symbol":"KLHL14","gene_name":"kelch like family member 14 [Source:HGNC Symbol;Acc:HGNC:29266]","synonyms":"KIAA1384","biotype":"protein_coding","ncbi_id":"57565","summary":"The protein encoded by this gene is a member of the Kelch-like gene family, whose members contain a BTB/POZ domain, a BACK domain, and several Kelch domains. The encoded protein possesses six Kelch domains and localizes to the endoplasmic reticulum, where it interacts with torsin-1A. [provided by RefSeq, Sep 2015]","start":32672671,"end":32773062,"strand":-1,"description":"kelch like family member 14 [Source:HGNC Symbol;Acc:HGNC:29266]"}, {"versioned_ensembl_gene_id":"ENSG00000228835.1","gene_symbol":"AC012123.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32769795,"end":32774413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253154.1","gene_symbol":"AC100801.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85839705,"end":85951083,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253448.1","gene_symbol":"IGLV3-6","gene_name":"immunoglobulin lambda variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5916]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28806","summary":null,"start":22850375,"end":22850624,"strand":1,"description":"immunoglobulin lambda variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5916]"}, {"versioned_ensembl_gene_id":"ENSG00000275157.1","gene_symbol":"AC068134.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":232368576,"end":232368697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254077.1","gene_symbol":"IGLV3-7","gene_name":"immunoglobulin lambda variable 3-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5917]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28805","summary":null,"start":22838602,"end":22838872,"strand":1,"description":"immunoglobulin lambda variable 3-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5917]"}, {"versioned_ensembl_gene_id":"ENSG00000237127.1","gene_symbol":"AC245028.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22834865,"end":22835117,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278196.3","gene_symbol":"IGLV2-8","gene_name":"immunoglobulin lambda variable 2-8 [Source:HGNC Symbol;Acc:HGNC:5895]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28817","summary":null,"start":22822658,"end":22823289,"strand":1,"description":"immunoglobulin lambda variable 2-8 [Source:HGNC Symbol;Acc:HGNC:5895]"}, {"versioned_ensembl_gene_id":"ENSG00000172167.7","gene_symbol":"MTBP","gene_name":"MDM2 binding protein [Source:HGNC Symbol;Acc:HGNC:7417]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27085","summary":"This gene encodes a protein that interacts with the oncoprotein mouse double minute 2. The encoded protein regulates progression through the cell cycle and may be involved in tumor formation. [provided by RefSeq, Aug 2012]","start":120445400,"end":120542133,"strand":1,"description":"MDM2 binding protein [Source:HGNC Symbol;Acc:HGNC:7417]"}, {"versioned_ensembl_gene_id":"ENSG00000211668.2","gene_symbol":"IGLV2-11","gene_name":"immunoglobulin lambda variable 2-11 [Source:HGNC Symbol;Acc:HGNC:5887]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28816","summary":null,"start":22792491,"end":22793007,"strand":1,"description":"immunoglobulin lambda variable 2-11 [Source:HGNC Symbol;Acc:HGNC:5887]"}, {"versioned_ensembl_gene_id":"ENSG00000064666.14","gene_symbol":"CNN2","gene_name":"calponin 2 [Source:HGNC Symbol;Acc:HGNC:2156]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1265","summary":"The protein encoded by this gene, which can bind actin, calmodulin, troponin C, and tropomyosin, may function in the structural organization of actin filaments. The encoded protein could play a role in smooth muscle contraction and cell adhesion. Several pseudogenes of this gene have been identified, and are present on chromosomes 1, 2, 3, 6, 9, 11, 13, 15, 16, 21 and 22. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2015]","start":1026581,"end":1039068,"strand":1,"description":"calponin 2 [Source:HGNC Symbol;Acc:HGNC:2156]"}, {"versioned_ensembl_gene_id":"ENSG00000242727.2","gene_symbol":"AC104687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76891034,"end":76891445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270244.1","gene_symbol":"AC104687.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76886029,"end":76886370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246792.2","gene_symbol":"AC106038.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90646441,"end":90656598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159899.14","gene_symbol":"NPR2","gene_name":"natriuretic peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:7944]","synonyms":"NPRB,GUCY2B,ANPRB,ANPb,AMDM","biotype":"protein_coding","ncbi_id":"4882","summary":"This gene encodes natriuretic peptide receptor B, one of two integral membrane receptors for natriuretic peptides. Both NPR1 and NPR2 contain five functional domains: an extracellular ligand-binding domain, a single membrane-spanning region, and intracellularly a protein kinase homology domain, a helical hinge region involved in oligomerization, and a carboxyl-terminal guanylyl cyclase catalytic domain. The protein is the primary receptor for C-type natriuretic peptide (CNP), which upon ligand binding exhibits greatly increased guanylyl cyclase activity. Mutations in this gene are the cause of acromesomelic dysplasia Maroteaux type. [provided by RefSeq, Jul 2008]","start":35792154,"end":35809732,"strand":1,"description":"natriuretic peptide receptor 2 [Source:HGNC Symbol;Acc:HGNC:7944]"}, {"versioned_ensembl_gene_id":"ENSG00000231392.1","gene_symbol":"AC244157.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22774529,"end":22774691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273517.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"EB6ActI,CD158H,EB6ActII,CD158H,EB6ActII,EB6ActI","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54847867,"end":54861881,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000272799.1","gene_symbol":"AC006238.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9912316,"end":9912849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248792.1","gene_symbol":"LINC00266-2P","gene_name":"long intergenic non-protein coding RNA 266-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38529]","synonyms":"NCRNA00266Y1,NCRNA00266B,NCRNA00266-2P","biotype":"unprocessed_pseudogene","ncbi_id":"100287785","summary":null,"start":24278681,"end":24291346,"strand":1,"description":"long intergenic non-protein coding RNA 266-2, pseudogene [Source:HGNC Symbol;Acc:HGNC:38529]"}, {"versioned_ensembl_gene_id":"ENSG00000233382.6","gene_symbol":"NKAPP1","gene_name":"NFKB activating protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26706]","synonyms":"FLJ36576,CXorf42","biotype":"transcribed_processed_pseudogene","ncbi_id":"158801","summary":null,"start":120120953,"end":120245267,"strand":-1,"description":"NFKB activating protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26706]"}, {"versioned_ensembl_gene_id":"ENSG00000164197.11","gene_symbol":"RNF180","gene_name":"ring finger protein 180 [Source:HGNC Symbol;Acc:HGNC:27752]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285671","summary":null,"start":64165844,"end":64372869,"strand":1,"description":"ring finger protein 180 [Source:HGNC Symbol;Acc:HGNC:27752]"}, {"versioned_ensembl_gene_id":"ENSG00000258545.5","gene_symbol":"RHOXF1-AS1","gene_name":"RHOXF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51582]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928969","summary":null,"start":120036236,"end":120146854,"strand":1,"description":"RHOXF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51582]"}, {"versioned_ensembl_gene_id":"ENSG00000197147.13","gene_symbol":"LRRC8B","gene_name":"leucine rich repeat containing 8 family member B [Source:HGNC Symbol;Acc:HGNC:30692]","synonyms":"TA-LRRP,KIAA0231","biotype":"protein_coding","ncbi_id":"23507","summary":null,"start":89524836,"end":89597864,"strand":1,"description":"leucine rich repeat containing 8 family member B [Source:HGNC Symbol;Acc:HGNC:30692]"}, {"versioned_ensembl_gene_id":"ENSG00000169627.7","gene_symbol":"BOLA2B","gene_name":"bolA family member 2B [Source:HGNC Symbol;Acc:HGNC:32479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654483","summary":"This gene is located within a region of a segmental duplication on chromosome 16 and is identical to BOLA2 (bolA family member 2). The product of this gene belongs to a family of proteins that are widely conserved and may be involved in iron maturation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":30192934,"end":30194306,"strand":-1,"description":"bolA family member 2B [Source:HGNC Symbol;Acc:HGNC:32479]"}, {"versioned_ensembl_gene_id":"ENSG00000268659.2","gene_symbol":"AL589863.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75642476,"end":75643106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260969.1","gene_symbol":"WWOX-AS1","gene_name":"WWOX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53169]","synonyms":"RP11-190D6.2","biotype":"antisense_RNA","ncbi_id":"102724047","summary":null,"start":78237362,"end":78241218,"strand":-1,"description":"WWOX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53169]"}, {"versioned_ensembl_gene_id":"ENSG00000243101.1","gene_symbol":"RPS3P7","gene_name":"ribosomal protein S3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36056]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645957","summary":null,"start":78825281,"end":78826006,"strand":1,"description":"ribosomal protein S3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36056]"}, {"versioned_ensembl_gene_id":"ENSG00000235032.1","gene_symbol":"BMP7-AS1","gene_name":"BMP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40096]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723590","summary":null,"start":57214872,"end":57215866,"strand":1,"description":"BMP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40096]"}, {"versioned_ensembl_gene_id":"ENSG00000253490.5","gene_symbol":"LINC02099","gene_name":"long intergenic non-protein coding RNA 2099 [Source:HGNC Symbol;Acc:HGNC:52953]","synonyms":"AC145110.1","biotype":"lincRNA","ncbi_id":"101929450","summary":null,"start":29748309,"end":29798492,"strand":1,"description":"long intergenic non-protein coding RNA 2099 [Source:HGNC Symbol;Acc:HGNC:52953]"}, {"versioned_ensembl_gene_id":"ENSG00000269186.1","gene_symbol":"LINC01082","gene_name":"long intergenic non-protein coding RNA 1082 [Source:HGNC Symbol;Acc:HGNC:49125]","synonyms":"TCONS_00024492","biotype":"lincRNA","ncbi_id":"100506542","summary":null,"start":86196181,"end":86199720,"strand":1,"description":"long intergenic non-protein coding RNA 1082 [Source:HGNC Symbol;Acc:HGNC:49125]"}, {"versioned_ensembl_gene_id":"ENSG00000248285.1","gene_symbol":"AC122707.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":63957893,"end":63981043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138821.12","gene_symbol":"SLC39A8","gene_name":"solute carrier family 39 member 8 [Source:HGNC Symbol;Acc:HGNC:20862]","synonyms":"BIGM103","biotype":"protein_coding","ncbi_id":"64116","summary":"This gene encodes a member of the SLC39 family of solute-carrier genes, which show structural characteristics of zinc transporters. The encoded protein is glycosylated and found in the plasma membrane and mitochondria, and functions in the cellular import of zinc at the onset of inflammation. It is also thought to be the primary transporter of the toxic cation cadmium, which is found in cigarette smoke. Multiple transcript variants encoding different isoforms have been found for this gene. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Oct 2008]","start":102251041,"end":102431258,"strand":-1,"description":"solute carrier family 39 member 8 [Source:HGNC Symbol;Acc:HGNC:20862]"}, {"versioned_ensembl_gene_id":"ENSG00000253853.1","gene_symbol":"AC246817.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2727318,"end":2822482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198876.12","gene_symbol":"DCAF12","gene_name":"DDB1 and CUL4 associated factor 12 [Source:HGNC Symbol;Acc:HGNC:19911]","synonyms":"TCC52,MGC1058,KIAA1892,DKFZP434O125,CT102,WDR40A","biotype":"protein_coding","ncbi_id":"25853","summary":"This gene encodes a WD repeat-containing protein that interacts with the COP9 signalosome, a macromolecular complex that interacts with cullin-RING E3 ligases and regulates their activity by hydrolyzing cullin-Nedd8 conjugates. [provided by RefSeq, Jul 2009]","start":34086387,"end":34127399,"strand":-1,"description":"DDB1 and CUL4 associated factor 12 [Source:HGNC Symbol;Acc:HGNC:19911]"}, {"versioned_ensembl_gene_id":"ENSG00000224802.2","gene_symbol":"TUBB4BP2","gene_name":"tubulin beta 4B class IVb pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42183]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418974","summary":null,"start":34109171,"end":34109968,"strand":-1,"description":"tubulin beta 4B class IVb pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42183]"}, {"versioned_ensembl_gene_id":"ENSG00000072080.10","gene_symbol":"SPP2","gene_name":"secreted phosphoprotein 2 [Source:HGNC Symbol;Acc:HGNC:11256]","synonyms":"SPP24","biotype":"protein_coding","ncbi_id":"6694","summary":"This gene encodes a secreted phosphoprotein that is a member of the cystatin superfamily. [provided by RefSeq, Oct 2008]","start":234050679,"end":234077134,"strand":1,"description":"secreted phosphoprotein 2 [Source:HGNC Symbol;Acc:HGNC:11256]"}, {"versioned_ensembl_gene_id":"ENSG00000227246.2","gene_symbol":"PSORS1C2","gene_name":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]","synonyms":"SPR1,C6orf17","biotype":"protein_coding","ncbi_id":"170680","summary":null,"start":31216078,"end":31217894,"strand":-1,"description":"psoriasis susceptibility 1 candidate 2 [Source:HGNC Symbol;Acc:HGNC:17199]"}, {"versioned_ensembl_gene_id":"ENSG00000280322.1","gene_symbol":"AL035425.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108725886,"end":108726948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232089.1","gene_symbol":"AC011233.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221162771,"end":221163053,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166262.15","gene_symbol":"FAM227B","gene_name":"family with sequence similarity 227 member B [Source:HGNC Symbol;Acc:HGNC:26543]","synonyms":"FLJ32800,C15orf33","biotype":"protein_coding","ncbi_id":"196951","summary":null,"start":49326962,"end":49620931,"strand":-1,"description":"family with sequence similarity 227 member B [Source:HGNC Symbol;Acc:HGNC:26543]"}, {"versioned_ensembl_gene_id":"ENSG00000162384.13","gene_symbol":"C1orf123","gene_name":"chromosome 1 open reading frame 123 [Source:HGNC Symbol;Acc:HGNC:26059]","synonyms":"FLJ20580","biotype":"protein_coding","ncbi_id":"54987","summary":null,"start":53214099,"end":53220617,"strand":-1,"description":"chromosome 1 open reading frame 123 [Source:HGNC Symbol;Acc:HGNC:26059]"}, {"versioned_ensembl_gene_id":"ENSG00000114573.9","gene_symbol":"ATP6V1A","gene_name":"ATPase H+ transporting V1 subunit A [Source:HGNC Symbol;Acc:HGNC:851]","synonyms":"VPP2,Vma1,VA68,ATP6V1A1,ATP6A1","biotype":"protein_coding","ncbi_id":"523","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c\", and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain A subunit isoforms and is found in all tissues. Transcript variants derived from alternative polyadenylation exist. [provided by RefSeq, Jul 2008]","start":113747019,"end":113812056,"strand":1,"description":"ATPase H+ transporting V1 subunit A [Source:HGNC Symbol;Acc:HGNC:851]"}, {"versioned_ensembl_gene_id":"ENSG00000282686.1","gene_symbol":"AC245519.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2495522,"end":2499428,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223903.1","gene_symbol":"RPL23P4","gene_name":"ribosomal protein L23 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36678]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270961","summary":null,"start":219697799,"end":219698214,"strand":1,"description":"ribosomal protein L23 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36678]"}, {"versioned_ensembl_gene_id":"ENSG00000249278.1","gene_symbol":"AC112249.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76509284,"end":76509719,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186715.10","gene_symbol":"MST1L","gene_name":"macrophage stimulating 1 like [Source:HGNC Symbol;Acc:HGNC:7390]","synonyms":"MSTP9,MSTP7,MST1P9,MSPL7,MSPL-7,D1F15S1A","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"11223","summary":null,"start":16754910,"end":16770237,"strand":-1,"description":"macrophage stimulating 1 like [Source:HGNC Symbol;Acc:HGNC:7390]"}, {"versioned_ensembl_gene_id":"ENSG00000282534.1","gene_symbol":"IMPDH1P5","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340780","summary":null,"start":77780337,"end":77781876,"strand":-1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:33960]"}, {"versioned_ensembl_gene_id":"ENSG00000063660.8","gene_symbol":"GPC1","gene_name":"glypican 1 [Source:HGNC Symbol;Acc:HGNC:4449]","synonyms":"glypican","biotype":"protein_coding","ncbi_id":"2817","summary":"Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. [provided by RefSeq, Jul 2008]","start":240435671,"end":240468078,"strand":1,"description":"glypican 1 [Source:HGNC Symbol;Acc:HGNC:4449]"}, {"versioned_ensembl_gene_id":"ENSG00000099849.14","gene_symbol":"RASSF7","gene_name":"Ras association domain family member 7 [Source:HGNC Symbol;Acc:HGNC:1166]","synonyms":"HRC1,HRAS1,C11orf13","biotype":"protein_coding","ncbi_id":"8045","summary":null,"start":560404,"end":564021,"strand":1,"description":"Ras association domain family member 7 [Source:HGNC Symbol;Acc:HGNC:1166]"}, {"versioned_ensembl_gene_id":"ENSG00000144815.15","gene_symbol":"NXPE3","gene_name":"neurexophilin and PC-esterase domain family member 3 [Source:HGNC Symbol;Acc:HGNC:28238]","synonyms":"MGC15606,FAM55C","biotype":"protein_coding","ncbi_id":"91775","summary":"This gene encodes a member of the neurexophilin family of neuropeptide-like glycoproteins. The encoded protein contains a variable N-terminal domain, a highly conserved neurexophilin and PC-esterase (NXPE) central domain, a short linker region, and a cysteine-rich C-terminal domain. This protein binds alpha neurexins, a group of presynaptic transmembrane receptors that promote adhesion between dendrites and axons. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":101779202,"end":101827392,"strand":1,"description":"neurexophilin and PC-esterase domain family member 3 [Source:HGNC Symbol;Acc:HGNC:28238]"}, {"versioned_ensembl_gene_id":"ENSG00000249474.1","gene_symbol":"AC020651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101823793,"end":101824998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106348.16","gene_symbol":"IMPDH1","gene_name":"inosine monophosphate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:6052]","synonyms":"sWSS2608,RP10,LCA11","biotype":"protein_coding","ncbi_id":"3614","summary":"The protein encoded by this gene acts as a homotetramer to regulate cell growth. The encoded protein is an enzyme that catalyzes the synthesis of xanthine monophosphate (XMP) from inosine-5'-monophosphate (IMP). This is the rate-limiting step in the de novo synthesis of guanine nucleotides. Defects in this gene are a cause of retinitis pigmentosa type 10 (RP10). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","start":128392277,"end":128410252,"strand":-1,"description":"inosine monophosphate dehydrogenase 1 [Source:HGNC Symbol;Acc:HGNC:6052]"}, {"versioned_ensembl_gene_id":"ENSG00000089199.9","gene_symbol":"CHGB","gene_name":"chromogranin B [Source:HGNC Symbol;Acc:HGNC:1930]","synonyms":"SgI,SCG1","biotype":"protein_coding","ncbi_id":"1114","summary":"This gene encodes a tyrosine-sulfated secretory protein abundant in peptidergic endocrine cells and neurons. This protein may serve as a precursor for regulatory peptides. [provided by RefSeq, Jan 2009]","start":5911430,"end":5925361,"strand":1,"description":"chromogranin B [Source:HGNC Symbol;Acc:HGNC:1930]"}, {"versioned_ensembl_gene_id":"ENSG00000267262.1","gene_symbol":"AC011444.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6067953,"end":6077119,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266983.1","gene_symbol":"AC011444.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5978403,"end":6020363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278277.1","gene_symbol":"GU182355.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771294,"end":54784697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223698.3","gene_symbol":"GOLGA6L11P","gene_name":"golgin A6 family-like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:23958]","synonyms":"GOLGA6L15P","biotype":"unprocessed_pseudogene","ncbi_id":"360024","summary":null,"start":24168187,"end":24174494,"strand":1,"description":"golgin A6 family-like 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:23958]"}, {"versioned_ensembl_gene_id":"ENSG00000161981.10","gene_symbol":"SNRNP25","gene_name":"small nuclear ribonucleoprotein U11/U12 subunit 25 [Source:HGNC Symbol;Acc:HGNC:14161]","synonyms":"U11/U12-25K,C16orf33","biotype":"protein_coding","ncbi_id":"79622","summary":"Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 25K protein that is a component of the U12-type spliceosome. [provided by RefSeq, Apr 2010]","start":53010,"end":57669,"strand":1,"description":"small nuclear ribonucleoprotein U11/U12 subunit 25 [Source:HGNC Symbol;Acc:HGNC:14161]"}, {"versioned_ensembl_gene_id":"ENSG00000100888.12","gene_symbol":"CHD8","gene_name":"chromodomain helicase DNA binding protein 8 [Source:HGNC Symbol;Acc:HGNC:20153]","synonyms":"KIAA1564,HELSNF1,DUPLIN","biotype":"protein_coding","ncbi_id":"57680","summary":"This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]","start":21385194,"end":21456126,"strand":-1,"description":"chromodomain helicase DNA binding protein 8 [Source:HGNC Symbol;Acc:HGNC:20153]"}, {"versioned_ensembl_gene_id":"ENSG00000278464.1","gene_symbol":"AC068506.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34892013,"end":34902885,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170638.9","gene_symbol":"TRABD","gene_name":"TraB domain containing [Source:HGNC Symbol;Acc:HGNC:28805]","synonyms":"PP2447","biotype":"protein_coding","ncbi_id":"80305","summary":null,"start":50185915,"end":50199598,"strand":1,"description":"TraB domain containing [Source:HGNC Symbol;Acc:HGNC:28805]"}, {"versioned_ensembl_gene_id":"ENSG00000243122.1","gene_symbol":"AC016304.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37490691,"end":37491103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228938.3","gene_symbol":"SNRPD2P1","gene_name":"small nuclear ribonucleoprotein D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31459]","synonyms":"SNRPD2P,bA478K7.1","biotype":"processed_pseudogene","ncbi_id":"119358","summary":null,"start":89978717,"end":89979070,"strand":1,"description":"small nuclear ribonucleoprotein D2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31459]"}, {"versioned_ensembl_gene_id":"ENSG00000259467.1","gene_symbol":"NDUFAF4P1","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44194]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100306975","summary":null,"start":49156329,"end":49156847,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44194]"}, {"versioned_ensembl_gene_id":"ENSG00000269416.5","gene_symbol":"LINC01224","gene_name":"long intergenic non-protein coding RNA 1224 [Source:HGNC Symbol;Acc:HGNC:49676]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104472717","summary":null,"start":23399233,"end":23416075,"strand":-1,"description":"long intergenic non-protein coding RNA 1224 [Source:HGNC Symbol;Acc:HGNC:49676]"}, {"versioned_ensembl_gene_id":"ENSG00000281788.1","gene_symbol":"AC093627.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186240,"end":197485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224124.3","gene_symbol":"POM121L10P","gene_name":"POM121 transmembrane nucleoporin like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:35448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646074","summary":null,"start":24657481,"end":24658765,"strand":-1,"description":"POM121 transmembrane nucleoporin like 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:35448]"}, {"versioned_ensembl_gene_id":"ENSG00000163154.5","gene_symbol":"TNFAIP8L2","gene_name":"TNF alpha induced protein 8 like 2 [Source:HGNC Symbol;Acc:HGNC:26277]","synonyms":"FLJ23467","biotype":"protein_coding","ncbi_id":"79626","summary":null,"start":151156629,"end":151159749,"strand":1,"description":"TNF alpha induced protein 8 like 2 [Source:HGNC Symbol;Acc:HGNC:26277]"}, {"versioned_ensembl_gene_id":"ENSG00000231605.5","gene_symbol":"LINC01363","gene_name":"long intergenic non-protein coding RNA 1363 [Source:HGNC Symbol;Acc:HGNC:50598]","synonyms":"RBSG4","biotype":"antisense_RNA","ncbi_id":"101928484","summary":null,"start":167175917,"end":167195792,"strand":-1,"description":"long intergenic non-protein coding RNA 1363 [Source:HGNC Symbol;Acc:HGNC:50598]"}, {"versioned_ensembl_gene_id":"ENSG00000226159.1","gene_symbol":"LINC01375","gene_name":"long intergenic non-protein coding RNA 1375 [Source:HGNC Symbol;Acc:HGNC:50632]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926924","summary":null,"start":89915489,"end":89957373,"strand":-1,"description":"long intergenic non-protein coding RNA 1375 [Source:HGNC Symbol;Acc:HGNC:50632]"}, {"versioned_ensembl_gene_id":"ENSG00000174989.12","gene_symbol":"FBXW8","gene_name":"F-box and WD repeat domain containing 8 [Source:HGNC Symbol;Acc:HGNC:13597]","synonyms":"FBXO29,FBX29,FBW8,FBW6","biotype":"protein_coding","ncbi_id":"26259","summary":"This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into three classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene contains a WD-40 domain, in addition to an F-box motif, so it belongs to the Fbw class. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":116910956,"end":117031148,"strand":1,"description":"F-box and WD repeat domain containing 8 [Source:HGNC Symbol;Acc:HGNC:13597]"}, {"versioned_ensembl_gene_id":"ENSG00000131373.14","gene_symbol":"HACL1","gene_name":"2-hydroxyacyl-CoA lyase 1 [Source:HGNC Symbol;Acc:HGNC:17856]","synonyms":"2-HPCL,PHYH2,HPCL","biotype":"protein_coding","ncbi_id":"26061","summary":null,"start":15560704,"end":15601852,"strand":-1,"description":"2-hydroxyacyl-CoA lyase 1 [Source:HGNC Symbol;Acc:HGNC:17856]"}, {"versioned_ensembl_gene_id":"ENSG00000277840.1","gene_symbol":"AC026368.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":117002463,"end":117003152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166441.12","gene_symbol":"RPL27A","gene_name":"ribosomal protein L27a [Source:HGNC Symbol;Acc:HGNC:10329]","synonyms":"L27A","biotype":"protein_coding","ncbi_id":"6157","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L15P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":8682411,"end":8714759,"strand":1,"description":"ribosomal protein L27a [Source:HGNC Symbol;Acc:HGNC:10329]"}, {"versioned_ensembl_gene_id":"ENSG00000259551.1","gene_symbol":"AC048382.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":84500378,"end":84502381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280560.1","gene_symbol":"AL138924.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89853906,"end":89914948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230939.1","gene_symbol":"AL591475.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8784178,"end":8785445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259538.1","gene_symbol":"UBE2Q2P11","gene_name":"ubiquitin conjugating enzyme E2 Q2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49522]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421767","summary":null,"start":84412773,"end":84421837,"strand":-1,"description":"ubiquitin conjugating enzyme E2 Q2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49522]"}, {"versioned_ensembl_gene_id":"ENSG00000152219.4","gene_symbol":"ARL14EP","gene_name":"ADP ribosylation factor like GTPase 14 effector protein [Source:HGNC Symbol;Acc:HGNC:26798]","synonyms":"FLJ38968,C11orf46,ARF7EP","biotype":"protein_coding","ncbi_id":"120534","summary":"The protein encoded by this gene is an effector protein. It interacts with ADP-ribosylation factor-like 14 [ARL14, also known as ADP-ribosylation factor 7 (ARF7)], beta-actin (ACTB) and actin-based motor protein myosin 1E (MYO1E). ARL14 is a small GTPase; it controls the export of major histocompatibility class II molecules by connecting to the actin network via this effector protein. [provided by RefSeq, Sep 2014]","start":30323051,"end":30338227,"strand":1,"description":"ADP ribosylation factor like GTPase 14 effector protein [Source:HGNC Symbol;Acc:HGNC:26798]"}, {"versioned_ensembl_gene_id":"ENSG00000284678.1","gene_symbol":"AL033527.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39801414,"end":39817460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284719.1","gene_symbol":"AL033527.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39799422,"end":39809450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000059573.8","gene_symbol":"ALDH18A1","gene_name":"aldehyde dehydrogenase 18 family member A1 [Source:HGNC Symbol;Acc:HGNC:9722]","synonyms":"SPG9,PYCS,P5CS,GSAS","biotype":"protein_coding","ncbi_id":"5832","summary":"This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases. Alternatively spliced transcript variants, encoding different isoforms, have been described for this gene. [provided by RefSeq, Jul 2008]","start":95605929,"end":95656706,"strand":-1,"description":"aldehyde dehydrogenase 18 family member A1 [Source:HGNC Symbol;Acc:HGNC:9722]"}, {"versioned_ensembl_gene_id":"ENSG00000197919.5","gene_symbol":"IFNA1","gene_name":"interferon alpha 1 [Source:HGNC Symbol;Acc:HGNC:5417]","synonyms":"IFNA@,IFNA13,IFN-alphaD,IFN-ALPHA,IFN,IFL","biotype":"protein_coding","ncbi_id":"3439","summary":"This gene is a member of the alpha interferon gene cluster on chromosome 9. The encoded cytokine is a member of the type I interferon family that is produced in response to viral infection as a key part of the innate immune response with potent antiviral, antiproliferative and immunomodulatory properties. This cytokine, like other type I interferons, binds a plasma membrane receptor made of IFNAR1 and IFNAR2 that is ubiquitously expressed, and thus is able to act on virtually all body cells. This cytokine is upregulated in preeclamptic placentas and is thought to be a mediator of preeclampsia. [provided by RefSeq, Aug 2020]","start":21440454,"end":21441316,"strand":1,"description":"interferon alpha 1 [Source:HGNC Symbol;Acc:HGNC:5417]"}, {"versioned_ensembl_gene_id":"ENSG00000235430.1","gene_symbol":"ZSWIM5P1","gene_name":"zinc finger SWIM-type containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43768]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130110","summary":null,"start":15768717,"end":15771426,"strand":-1,"description":"zinc finger SWIM-type containing 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43768]"}, {"versioned_ensembl_gene_id":"ENSG00000283578.1","gene_symbol":"MTND5P42","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52321]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729157","summary":null,"start":89786610,"end":89787107,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52321]"}, {"versioned_ensembl_gene_id":"ENSG00000237691.1","gene_symbol":"IFNWP2","gene_name":"interferon omega 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5452]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"646581","summary":null,"start":21420234,"end":21420813,"strand":1,"description":"interferon omega 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:5452]"}, {"versioned_ensembl_gene_id":"ENSG00000261540.1","gene_symbol":"AC079414.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78014683,"end":78059454,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232065.1","gene_symbol":"LINC01063","gene_name":"long intergenic non-protein coding RNA 1063 [Source:HGNC Symbol;Acc:HGNC:49092]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929769","summary":null,"start":196631498,"end":196632587,"strand":-1,"description":"long intergenic non-protein coding RNA 1063 [Source:HGNC Symbol;Acc:HGNC:49092]"}, {"versioned_ensembl_gene_id":"ENSG00000130706.12","gene_symbol":"ADRM1","gene_name":"adhesion regulating molecule 1 [Source:HGNC Symbol;Acc:HGNC:15759]","synonyms":"Rpn13,GP110,ARM1","biotype":"protein_coding","ncbi_id":"11047","summary":"This gene encodes a member of the adhesion regulating molecule 1 protein family. The encoded protein is a component of the proteasome where it acts as a ubiquitin receptor and recruits the deubiquitinating enzyme, ubiquitin carboxyl-terminal hydrolase L5. Increased levels of the encoded protein are associated with increased cell adhesion, which is likely an indirect effect of this intracellular protein. Dysregulation of this gene has been implicated in carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":62302093,"end":62308862,"strand":1,"description":"adhesion regulating molecule 1 [Source:HGNC Symbol;Acc:HGNC:15759]"}, {"versioned_ensembl_gene_id":"ENSG00000270742.1","gene_symbol":"AC096947.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":61124733,"end":61125202,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132356.11","gene_symbol":"PRKAA1","gene_name":"protein kinase AMP-activated catalytic subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:9376]","synonyms":"AMPKa1","biotype":"protein_coding","ncbi_id":"5562","summary":"The protein encoded by this gene belongs to the ser/thr protein kinase family. It is the catalytic subunit of the 5'-prime-AMP-activated protein kinase (AMPK). AMPK is a cellular energy sensor conserved in all eukaryotic cells. The kinase activity of AMPK is activated by the stimuli that increase the cellular AMP/ATP ratio. AMPK regulates the activities of a number of key metabolic enzymes through phosphorylation. It protects cells from stresses that cause ATP depletion by switching off ATP-consuming biosynthetic pathways. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":40759379,"end":40798374,"strand":-1,"description":"protein kinase AMP-activated catalytic subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:9376]"}, {"versioned_ensembl_gene_id":"ENSG00000259683.1","gene_symbol":"AC243562.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84389729,"end":84395903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253680.1","gene_symbol":"AC093331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85617344,"end":85617512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259672.1","gene_symbol":"AC087612.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63098870,"end":63110403,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259441.2","gene_symbol":"AC079075.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89752296,"end":89753493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000157240.3","gene_symbol":"FZD1","gene_name":"frizzled class receptor 1 [Source:HGNC Symbol;Acc:HGNC:4038]","synonyms":"DKFZp564G072","biotype":"protein_coding","ncbi_id":"8321","summary":" Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD1 protein contains a signal peptide, a cysteine-rich domain in the N-terminal extracellular region, 7 transmembrane domains, and a C-terminal PDZ domain-binding motif. The FZD1 transcript is expressed in various tissues. [provided by RefSeq, Jul 2008]","start":91264364,"end":91271326,"strand":1,"description":"frizzled class receptor 1 [Source:HGNC Symbol;Acc:HGNC:4038]"}, {"versioned_ensembl_gene_id":"ENSG00000279201.1","gene_symbol":"AC073263.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":74191388,"end":74192245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236637.4","gene_symbol":"IFNA4","gene_name":"interferon alpha 4 [Source:HGNC Symbol;Acc:HGNC:5425]","synonyms":"MGC142200,IFN-alpha4a","biotype":"protein_coding","ncbi_id":"3441","summary":null,"start":21186694,"end":21187671,"strand":-1,"description":"interferon alpha 4 [Source:HGNC Symbol;Acc:HGNC:5425]"}, {"versioned_ensembl_gene_id":"ENSG00000230614.3","gene_symbol":"DYNLL1P7","gene_name":"dynein light chain LC8-type 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49658]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729630","summary":null,"start":85381118,"end":85381375,"strand":-1,"description":"dynein light chain LC8-type 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:49658]"}, {"versioned_ensembl_gene_id":"ENSG00000177047.6","gene_symbol":"IFNW1","gene_name":"interferon omega 1 [Source:HGNC Symbol;Acc:HGNC:5448]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3467","summary":"The protein encoded by this gene is an interferon and possesses antiviral activity. The encoded protein binds to the interferon alpha/beta receptor but not to the interferon gamma receptor. This intronless gene has several pseudogenes spread throughout the genome. [provided by RefSeq, Nov 2015]","start":21140214,"end":21142145,"strand":-1,"description":"interferon omega 1 [Source:HGNC Symbol;Acc:HGNC:5448]"}, {"versioned_ensembl_gene_id":"ENSG00000280086.1","gene_symbol":"AC026887.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":11395808,"end":11398792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085185.15","gene_symbol":"BCORL1","gene_name":"BCL6 corepressor like 1 [Source:HGNC Symbol;Acc:HGNC:25657]","synonyms":"CXorf10,FLJ11362","biotype":"protein_coding","ncbi_id":"63035","summary":"The protein encoded by this gene is a transcriptional corepressor that is found tethered to promoter regions by DNA-binding proteins. The encoded protein can interact with several different class II histone deacetylases to repress transcription. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","start":129981107,"end":130058083,"strand":1,"description":"BCL6 corepressor like 1 [Source:HGNC Symbol;Acc:HGNC:25657]"}, {"versioned_ensembl_gene_id":"ENSG00000283524.1","gene_symbol":"AC183089.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21971728,"end":21972643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269107.1","gene_symbol":"AC092329.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23257255,"end":23274232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227245.1","gene_symbol":"AC092042.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43087479,"end":43088068,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229213.1","gene_symbol":"AL033527.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39795843,"end":39795996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075643.5","gene_symbol":"MOCOS","gene_name":"molybdenum cofactor sulfurase [Source:HGNC Symbol;Acc:HGNC:18234]","synonyms":"MOS,HMCS,FLJ20733","biotype":"protein_coding","ncbi_id":"55034","summary":"This gene encodes an enzyme that sulfurates the molybdenum cofactor which is required for activation of the xanthine dehydrogenase (XDH) and aldehyde oxidase (AO) enzymes. XDH catalyzes the conversion of hypoxanthine to uric acid via xanthine, as well as the conversion of allopurinol to oxypurinol, and pyrazinamide to 5-hydroxy pyrazinamide. Mutations in this gene cause the metabolic disorder classical xanthinuria type II which is characterized by the loss of XDH/XO and AO enzyme activity, decreased levels of uric acid in the urine, increased levels of xanthine and hypoxanthine in the serum and urine, formation of xanthine stones in the urinary tract, and myositis due to tissue deposition of xanthine. [provided by RefSeq, Apr 2017]","start":36187519,"end":36272157,"strand":1,"description":"molybdenum cofactor sulfurase [Source:HGNC Symbol;Acc:HGNC:18234]"}, {"versioned_ensembl_gene_id":"ENSG00000110628.13","gene_symbol":"SLC22A18","gene_name":"solute carrier family 22 member 18 [Source:HGNC Symbol;Acc:HGNC:10964]","synonyms":"TSSC5,SLC22A1L,ORCTL2,ITM,IMPT1,BWSCR1A,BWR1A","biotype":"protein_coding","ncbi_id":"5002","summary":"This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015]","start":2899721,"end":2925246,"strand":1,"description":"solute carrier family 22 member 18 [Source:HGNC Symbol;Acc:HGNC:10964]"}, {"versioned_ensembl_gene_id":"ENSG00000136231.13","gene_symbol":"IGF2BP3","gene_name":"insulin like growth factor 2 mRNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:28868]","synonyms":"IMP3,IMP-3,CT98","biotype":"protein_coding","ncbi_id":"10643","summary":"The protein encoded by this gene is primarily found in the nucleolus, where it can bind to the 5' UTR of the insulin-like growth factor II leader 3 mRNA and may repress translation of insulin-like growth factor II during late development. The encoded protein contains several KH domains, which are important in RNA binding and are known to be involved in RNA synthesis and metabolism. A pseudogene exists on chromosome 7, and there are putative pseudogenes on other chromosomes. [provided by RefSeq, Jul 2008]","start":23310209,"end":23470467,"strand":-1,"description":"insulin like growth factor 2 mRNA binding protein 3 [Source:HGNC Symbol;Acc:HGNC:28868]"}, {"versioned_ensembl_gene_id":"ENSG00000182093.14","gene_symbol":"WRB","gene_name":"tryptophan rich basic protein [Source:HGNC Symbol;Acc:HGNC:12790]","synonyms":"GET1,CHD5","biotype":"protein_coding","ncbi_id":"7485","summary":"This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017]","start":39380244,"end":39428528,"strand":1,"description":"tryptophan rich basic protein [Source:HGNC Symbol;Acc:HGNC:12790]"}, {"versioned_ensembl_gene_id":"ENSG00000254827.5","gene_symbol":"SLC22A18AS","gene_name":"solute carrier family 22 member 18 antisense [Source:HGNC Symbol;Acc:HGNC:10965]","synonyms":"BWR1B,SLC22A1LS,p27-BWR1B,ORCTL2S,BWSCR1B","biotype":"protein_coding","ncbi_id":"5003","summary":null,"start":2887780,"end":2903740,"strand":-1,"description":"solute carrier family 22 member 18 antisense [Source:HGNC Symbol;Acc:HGNC:10965]"}, {"versioned_ensembl_gene_id":"ENSG00000232627.1","gene_symbol":"AC021876.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23365618,"end":23365976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250890.1","gene_symbol":"AL117351.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":93926032,"end":93926188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231171.3","gene_symbol":"LINC01098","gene_name":"long intergenic non-protein coding RNA 1098 [Source:HGNC Symbol;Acc:HGNC:27731]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285501","summary":null,"start":177728757,"end":177990750,"strand":1,"description":"long intergenic non-protein coding RNA 1098 [Source:HGNC Symbol;Acc:HGNC:27731]"}, {"versioned_ensembl_gene_id":"ENSG00000114631.10","gene_symbol":"PODXL2","gene_name":"podocalyxin like 2 [Source:HGNC Symbol;Acc:HGNC:17936]","synonyms":"PODLX2,endoglycan","biotype":"protein_coding","ncbi_id":"50512","summary":"This gene is a member of the CD34 family of cell surface transmembrane proteins, which are characterized by an N-terminal extracellular mucin domain, globular and stalk domains, a single pass transmembrane region, and a charged cytoplasmic tail. The encoded protein is a ligand for vascular selectins. [provided by RefSeq, Oct 2012]","start":127629181,"end":127672809,"strand":1,"description":"podocalyxin like 2 [Source:HGNC Symbol;Acc:HGNC:17936]"}, {"versioned_ensembl_gene_id":"ENSG00000234970.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29983843,"end":29984720,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000134758.13","gene_symbol":"RNF138","gene_name":"ring finger protein 138 [Source:HGNC Symbol;Acc:HGNC:17765]","synonyms":"STRIN,NARF","biotype":"protein_coding","ncbi_id":"51444","summary":"The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":32091855,"end":32131561,"strand":1,"description":"ring finger protein 138 [Source:HGNC Symbol;Acc:HGNC:17765]"}, {"versioned_ensembl_gene_id":"ENSG00000275393.1","gene_symbol":"AC018695.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":85697335,"end":85697868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264644.1","gene_symbol":"KRT18P8","gene_name":"keratin 18 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31093]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"125242","summary":null,"start":9678248,"end":9679493,"strand":-1,"description":"keratin 18 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31093]"}, {"versioned_ensembl_gene_id":"ENSG00000101695.8","gene_symbol":"RNF125","gene_name":"ring finger protein 125 [Source:HGNC Symbol;Acc:HGNC:21150]","synonyms":"FLJ20456","biotype":"protein_coding","ncbi_id":"54941","summary":"This gene encodes a novel E3 ubiquitin ligase that contains a RING finger domain in the N-terminus and three zinc-binding and one ubiquitin-interacting motif in the C-terminus. As a result of myristoylation, this protein associates with membranes and is primarily localized to intracellular membrane systems. The encoded protein may function as a positive regulator in the T-cell receptor signaling pathway. [provided by RefSeq, Mar 2012]","start":32018372,"end":32073213,"strand":1,"description":"ring finger protein 125 [Source:HGNC Symbol;Acc:HGNC:21150]"}, {"versioned_ensembl_gene_id":"ENSG00000213578.5","gene_symbol":"CPLX3","gene_name":"complexin 3 [Source:HGNC Symbol;Acc:HGNC:27652]","synonyms":"CPX-III","biotype":"protein_coding","ncbi_id":"594855","summary":null,"start":74826547,"end":74831802,"strand":1,"description":"complexin 3 [Source:HGNC Symbol;Acc:HGNC:27652]"}, {"versioned_ensembl_gene_id":"ENSG00000261515.1","gene_symbol":"AC106785.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35836886,"end":35837732,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235743.1","gene_symbol":"AL139231.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23337711,"end":23346560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245080.7","gene_symbol":"AC068189.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95066808,"end":95073182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261620.1","gene_symbol":"AC106785.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35802869,"end":35803280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235243.1","gene_symbol":"AC093716.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":84847877,"end":84848253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240426.1","gene_symbol":"AC096743.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76401251,"end":76401569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228664.1","gene_symbol":"AL513480.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":182328497,"end":182329007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248388.5","gene_symbol":"AC093801.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176669621,"end":176706145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234722.3","gene_symbol":"LINC01287","gene_name":"long intergenic non-protein coding RNA 1287 [Source:HGNC Symbol;Acc:HGNC:50351]","synonyms":"TCONS_l2_00027522","biotype":"lincRNA","ncbi_id":"103724390","summary":null,"start":153399920,"end":153413963,"strand":-1,"description":"long intergenic non-protein coding RNA 1287 [Source:HGNC Symbol;Acc:HGNC:50351]"}, {"versioned_ensembl_gene_id":"ENSG00000102879.15","gene_symbol":"CORO1A","gene_name":"coronin 1A [Source:HGNC Symbol;Acc:HGNC:2252]","synonyms":"p57,HCORO1,coronin-1","biotype":"protein_coding","ncbi_id":"11151","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. A related pseudogene has been defined on chromosome 16. [provided by RefSeq, Sep 2010]","start":30182827,"end":30189076,"strand":1,"description":"coronin 1A [Source:HGNC Symbol;Acc:HGNC:2252]"}, {"versioned_ensembl_gene_id":"ENSG00000260282.1","gene_symbol":"EIF4EBP2P2","gene_name":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49317]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100190923","summary":null,"start":42581156,"end":42581488,"strand":-1,"description":"eukaryotic translation initiation factor 4E binding protein 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49317]"}, {"versioned_ensembl_gene_id":"ENSG00000263243.2","gene_symbol":"KRT12","gene_name":"keratin 12 [Source:HGNC Symbol;Acc:HGNC:6414]","synonyms":"K12","biotype":"protein_coding","ncbi_id":"3859","summary":"KRT12 encodes the type I intermediate filament chain keratin 12, expressed in corneal epithelia. Mutations in this gene lead to Meesmann corneal dystrophy. [provided by RefSeq, Jul 2008]","start":40861303,"end":40867210,"strand":-1,"description":"keratin 12 [Source:HGNC Symbol;Acc:HGNC:6414]"}, {"versioned_ensembl_gene_id":"ENSG00000101473.16","gene_symbol":"ACOT8","gene_name":"acyl-CoA thioesterase 8 [Source:HGNC Symbol;Acc:HGNC:15919]","synonyms":"PTE1,PTE-2,NAP1,hTE,hACTE-III","biotype":"protein_coding","ncbi_id":"10005","summary":"The protein encoded by this gene is a peroxisomal thioesterase that appears to be involved more in the oxidation of fatty acids rather than in their formation. The encoded protein can bind to the human immunodeficiency virus-1 protein Nef, and mediate Nef-induced down-regulation of CD4 in T-cells. [provided by RefSeq, Oct 2010]","start":45841721,"end":45857406,"strand":-1,"description":"acyl-CoA thioesterase 8 [Source:HGNC Symbol;Acc:HGNC:15919]"}, {"versioned_ensembl_gene_id":"ENSG00000163749.17","gene_symbol":"CCDC158","gene_name":"coiled-coil domain containing 158 [Source:HGNC Symbol;Acc:HGNC:26374]","synonyms":"FLJ25770","biotype":"protein_coding","ncbi_id":"339965","summary":null,"start":76312997,"end":76421868,"strand":-1,"description":"coiled-coil domain containing 158 [Source:HGNC Symbol;Acc:HGNC:26374]"}, {"versioned_ensembl_gene_id":"ENSG00000123575.8","gene_symbol":"FAM199X","gene_name":"family with sequence similarity 199, X-linked [Source:HGNC Symbol;Acc:HGNC:25195]","synonyms":"CXorf39","biotype":"protein_coding","ncbi_id":"139231","summary":null,"start":104166620,"end":104195902,"strand":1,"description":"family with sequence similarity 199, X-linked [Source:HGNC Symbol;Acc:HGNC:25195]"}, {"versioned_ensembl_gene_id":"ENSG00000277232.2","gene_symbol":"GTSE1-AS1","gene_name":"GTSE1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27163]","synonyms":null,"biotype":"lincRNA","ncbi_id":"150384","summary":null,"start":46295143,"end":46296660,"strand":-1,"description":"GTSE1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:27163]"}, {"versioned_ensembl_gene_id":"ENSG00000236183.2","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"G6c,C6orf24,NG24","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31706055,"end":31709252,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000234184.5","gene_symbol":"LINC01781","gene_name":"long intergenic non-protein coding RNA 1781 [Source:HGNC Symbol;Acc:HGNC:52571]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927412","summary":null,"start":80535755,"end":80646788,"strand":1,"description":"long intergenic non-protein coding RNA 1781 [Source:HGNC Symbol;Acc:HGNC:52571]"}, {"versioned_ensembl_gene_id":"ENSG00000236077.2","gene_symbol":"BX119904.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":116669810,"end":116680303,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232345.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29960191,"end":29961854,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000232936.5","gene_symbol":"AL157400.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89645282,"end":89650667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164815.10","gene_symbol":"ORC5","gene_name":"origin recognition complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:8491]","synonyms":"PPP1R117,ORC5T,Orc5p,ORC5L","biotype":"protein_coding","ncbi_id":"5001","summary":"The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Oct 2010]","start":104126341,"end":104208047,"strand":-1,"description":"origin recognition complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:8491]"}, {"versioned_ensembl_gene_id":"ENSG00000232585.1","gene_symbol":"OFD1P12Y","gene_name":"OFD1 pseudogene 12, Y-linked [Source:HGNC Symbol;Acc:HGNC:23884]","synonyms":"OFDYP12,OFD1PY12,OFD1P12","biotype":"unprocessed_pseudogene","ncbi_id":"386696","summary":null,"start":23972780,"end":23995081,"strand":1,"description":"OFD1 pseudogene 12, Y-linked [Source:HGNC Symbol;Acc:HGNC:23884]"}, {"versioned_ensembl_gene_id":"ENSG00000068323.16","gene_symbol":"TFE3","gene_name":"transcription factor binding to IGHM enhancer 3 [Source:HGNC Symbol;Acc:HGNC:11752]","synonyms":"TFEA,bHLHe33","biotype":"protein_coding","ncbi_id":"7030","summary":"This gene encodes a basic helix-loop-helix domain-containing transcription factor that binds MUE3-type E-box sequences in the promoter of genes. The encoded protein promotes the expression of genes downstream of transforming growth factor beta (TGF-beta) signaling. This gene may be involved in chromosomal translocations in renal cell carcinomas and other cancers, resulting in the production of fusion proteins. Translocation partners include PRCC (papillary renal cell carcinoma), NONO (non-POU domain containing, octamer-binding), and ASPSCR1 (alveolar soft part sarcoma chromosome region, candidate 1), among other genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":49028726,"end":49043486,"strand":-1,"description":"transcription factor binding to IGHM enhancer 3 [Source:HGNC Symbol;Acc:HGNC:11752]"}, {"versioned_ensembl_gene_id":"ENSG00000276959.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156123,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000224287.2","gene_symbol":"MSL3P1","gene_name":"MSL complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17837]","synonyms":"MSL3L2","biotype":"transcribed_processed_pseudogene","ncbi_id":"151507","summary":null,"start":233865437,"end":233868444,"strand":-1,"description":"MSL complex subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17837]"}, {"versioned_ensembl_gene_id":"ENSG00000282075.1","gene_symbol":"AC093614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149303,"end":155171,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273495.1","gene_symbol":"CUBNP2","gene_name":"cubilin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44984]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100289280","summary":null,"start":45232026,"end":45247361,"strand":-1,"description":"cubilin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44984]"}, {"versioned_ensembl_gene_id":"ENSG00000227289.1","gene_symbol":"HSFY3P","gene_name":"heat shock transcription factor, Y-linked 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:37119]","synonyms":"HSFYP2","biotype":"unprocessed_pseudogene","ncbi_id":"442479","summary":null,"start":2881683,"end":2883652,"strand":-1,"description":"heat shock transcription factor, Y-linked 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:37119]"}, {"versioned_ensembl_gene_id":"ENSG00000250263.1","gene_symbol":"LINC02509","gene_name":"long intergenic non-protein coding RNA 2509 [Source:HGNC Symbol;Acc:HGNC:53498]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377556","summary":null,"start":176875702,"end":176880605,"strand":1,"description":"long intergenic non-protein coding RNA 2509 [Source:HGNC Symbol;Acc:HGNC:53498]"}, {"versioned_ensembl_gene_id":"ENSG00000231376.1","gene_symbol":"HMGN2P16","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:31330]","synonyms":"HMGN2L,Em:AL513423.2","biotype":"processed_pseudogene","ncbi_id":"728234","summary":null,"start":15588355,"end":15588615,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:31330]"}, {"versioned_ensembl_gene_id":"ENSG00000180772.6","gene_symbol":"AGTR2","gene_name":"angiotensin II receptor type 2 [Source:HGNC Symbol;Acc:HGNC:338]","synonyms":"MRX88,AT2","biotype":"protein_coding","ncbi_id":"186","summary":"The protein encoded by this gene belongs to the G-protein coupled receptor 1 family, and functions as a receptor for angiotensin II. It is an intergral membrane protein that is highly expressed in fetus and in neonates, but scantily in adult tissues, except brain, adrenal medulla, and atretic ovary. This receptor has been shown to mediate programmed cell death and this apoptotic function may play an important role in developmental biology and pathophysiology. Mutations in this gene are been associated with X-linked cognitive disability. Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) and SARS-CoV-2 infection results in down-regulation of angiotensin converting enzyme-2 (ACE2) receptors, the effects of which, triggers serious inflammatory lesions in the tissues involved, primarily in the lungs. The inflammatory reaction appears to be mediated by angiotensin II derivatives, including the angiotensin AT2 receptor which has been found to be upregulated in bronchoalveolar lavage samples from Coronavirus disease 2019 (COVID19) patients. [provided by RefSeq, Jul 2020]","start":116170722,"end":116174972,"strand":1,"description":"angiotensin II receptor type 2 [Source:HGNC Symbol;Acc:HGNC:338]"}, {"versioned_ensembl_gene_id":"ENSG00000128917.6","gene_symbol":"DLL4","gene_name":"delta like canonical Notch ligand 4 [Source:HGNC Symbol;Acc:HGNC:2910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54567","summary":"This gene is a homolog of the Drosophila delta gene. The delta gene family encodes Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. [provided by RefSeq, Jul 2008]","start":40929340,"end":40939072,"strand":1,"description":"delta like canonical Notch ligand 4 [Source:HGNC Symbol;Acc:HGNC:2910]"}, {"versioned_ensembl_gene_id":"ENSG00000231423.1","gene_symbol":"RAB9AP5","gene_name":"RAB9A, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38109]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287234","summary":null,"start":23956569,"end":23960218,"strand":1,"description":"RAB9A, member RAS oncogene family pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38109]"}, {"versioned_ensembl_gene_id":"ENSG00000165731.18","gene_symbol":"RET","gene_name":"ret proto-oncogene [Source:HGNC Symbol;Acc:HGNC:9967]","synonyms":"MTC1,MEN2B,MEN2A,HSCR1,CDHR16,CDHF12,RET51,PTC","biotype":"protein_coding","ncbi_id":"5979","summary":"This gene encodes a transmembrane receptor and member of the tyrosine protein kinase family of proteins. Binding of ligands such as GDNF (glial cell-line derived neurotrophic factor) and other related proteins to the encoded receptor stimulates receptor dimerization and activation of downstream signaling pathways that play a role in cell differentiation, growth, migration and survival. The encoded receptor is important in development of the nervous system, and the development of organs and tissues derived from the neural crest. This proto-oncogene can undergo oncogenic activation through both cytogenetic rearrangement and activating point mutations. Mutations in this gene are associated with Hirschsprung disease and central hypoventilation syndrome and have been identified in patients with renal agenesis. [provided by RefSeq, Sep 2017]","start":43077027,"end":43130351,"strand":1,"description":"ret proto-oncogene [Source:HGNC Symbol;Acc:HGNC:9967]"}, {"versioned_ensembl_gene_id":"ENSG00000187498.14","gene_symbol":"COL4A1","gene_name":"collagen type IV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2202]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1282","summary":"This gene encodes a type IV collagen alpha protein. Type IV collagen proteins are integral components of basement membranes. This gene shares a bidirectional promoter with a paralogous gene on the opposite strand. The protein consists of an amino-terminal 7S domain, a triple-helix forming collagenous domain, and a carboxy-terminal non-collagenous domain. It functions as part of a heterotrimer and interacts with other extracellular matrix components such as perlecans, proteoglycans, and laminins. In addition, proteolytic cleavage of the non-collagenous carboxy-terminal domain results in a biologically active fragment known as arresten, which has anti-angiogenic and tumor suppressor properties. Mutations in this gene cause porencephaly, cerebrovascular disease, and renal and muscular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":110148963,"end":110307149,"strand":-1,"description":"collagen type IV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2202]"}, {"versioned_ensembl_gene_id":"ENSG00000170275.14","gene_symbol":"CRTAP","gene_name":"cartilage associated protein [Source:HGNC Symbol;Acc:HGNC:2379]","synonyms":"P3H5,LEPREL3,CASP","biotype":"protein_coding","ncbi_id":"10491","summary":"The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass. [provided by RefSeq, Jul 2008]","start":33113979,"end":33147773,"strand":1,"description":"cartilage associated protein [Source:HGNC Symbol;Acc:HGNC:2379]"}, {"versioned_ensembl_gene_id":"ENSG00000249844.1","gene_symbol":"OR7E43P","gene_name":"olfactory receptor family 7 subfamily E member 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:8417]","synonyms":"OR4-116","biotype":"unprocessed_pseudogene","ncbi_id":"26475","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4174319,"end":4175238,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 43 pseudogene [Source:HGNC Symbol;Acc:HGNC:8417]"}, {"versioned_ensembl_gene_id":"ENSG00000213478.2","gene_symbol":"CFL1P2","gene_name":"cofilin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1878]","synonyms":"CFLP2,CFLL2","biotype":"processed_pseudogene","ncbi_id":"391039","summary":null,"start":51157788,"end":51158471,"strand":-1,"description":"cofilin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1878]"}, {"versioned_ensembl_gene_id":"ENSG00000225248.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"OTTHUMG00000086663,BPG126D10.10","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29574058,"end":29574347,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000112578.9","gene_symbol":"BYSL","gene_name":"bystin like [Source:HGNC Symbol;Acc:HGNC:1157]","synonyms":"Enp1","biotype":"protein_coding","ncbi_id":"705","summary":"Bystin is expressed as a 2-kb major transcript and a 3.6-kb minor transcript in SNG-M cells and in human trophoblastic teratocarcinoma HT-H cells. Protein binding assays determined that bystin binds directly to trophinin and tastin, and that binding is enhanced when cytokeratins 8 and 18 are present. Immunocytochemistry of HT-H cells showed that bystin colocalizes with trophinin, tastin, and the cytokeratins, suggesting that these molecules form a complex in trophectoderm cells at the time of implantation. Using immunohistochemistry it was determined that trophinin and bystin are found in the placenta from the sixth week of pregnancy. Both proteins were localized in the cytoplasm of the syncytiotrophoblast in the chorionic villi and in endometrial decidual cells at the uteroplacental interface. After week 10, the levels of trophinin, tastin, and bystin decreased and then disappeared from placental villi. [provided by RefSeq, Jul 2008]","start":41921188,"end":41933046,"strand":1,"description":"bystin like [Source:HGNC Symbol;Acc:HGNC:1157]"}, {"versioned_ensembl_gene_id":"ENSG00000254049.1","gene_symbol":"NRG1-IT3","gene_name":"NRG1 intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:43635]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874286","summary":null,"start":32440746,"end":32442725,"strand":1,"description":"NRG1 intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:43635]"}, {"versioned_ensembl_gene_id":"ENSG00000170919.15","gene_symbol":"TPT1-AS1","gene_name":"TPT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43686]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100190939","summary":null,"start":45341345,"end":45393413,"strand":1,"description":"TPT1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43686]"}, {"versioned_ensembl_gene_id":"ENSG00000072864.14","gene_symbol":"NDE1","gene_name":"nudE neurodevelopment protein 1 [Source:HGNC Symbol;Acc:HGNC:17619]","synonyms":"NDE,FLJ20101,nudE","biotype":"protein_coding","ncbi_id":"54820","summary":"This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":15643267,"end":15726353,"strand":1,"description":"nudE neurodevelopment protein 1 [Source:HGNC Symbol;Acc:HGNC:17619]"}, {"versioned_ensembl_gene_id":"ENSG00000228918.3","gene_symbol":"LINC01344","gene_name":"long intergenic non-protein coding RNA 1344 [Source:HGNC Symbol;Acc:HGNC:50554]","synonyms":null,"biotype":"lincRNA","ncbi_id":"400799","summary":null,"start":182129310,"end":182314061,"strand":-1,"description":"long intergenic non-protein coding RNA 1344 [Source:HGNC Symbol;Acc:HGNC:50554]"}, {"versioned_ensembl_gene_id":"ENSG00000259798.1","gene_symbol":"AC138625.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71113352,"end":71114000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183807.7","gene_symbol":"FAM162B","gene_name":"family with sequence similarity 162 member B [Source:HGNC Symbol;Acc:HGNC:21549]","synonyms":"C6orf189,bA86F4.2","biotype":"protein_coding","ncbi_id":"221303","summary":null,"start":116752197,"end":116765723,"strand":-1,"description":"family with sequence similarity 162 member B [Source:HGNC Symbol;Acc:HGNC:21549]"}, {"versioned_ensembl_gene_id":"ENSG00000259833.5","gene_symbol":"AC138625.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":71080866,"end":71093667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133112.16","gene_symbol":"TPT1","gene_name":"tumor protein, translationally-controlled 1 [Source:HGNC Symbol;Acc:HGNC:12022]","synonyms":"TCTP,fortilin","biotype":"protein_coding","ncbi_id":"7178","summary":"This gene encodes a protein that is a regulator of cellular growth and proliferation. Its mRNA is highly structured and contains an oligopyrimidine tract (5'-TOP) in its 5' untranslated region that functions to repress its translation under quiescent conditions. The encoded protein is involved in a variety of cellular pathways, including apoptosis, protein synthesis and cell division. It binds to and stabilizes microtubules, and removal of this protein through phosphorylation is required for progression through mitotic and meiotic cell divisions. This gene is known to play a role in carcinogenesis, and is upregulated in some cancer cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]","start":45333471,"end":45341370,"strand":-1,"description":"tumor protein, translationally-controlled 1 [Source:HGNC Symbol;Acc:HGNC:12022]"}, {"versioned_ensembl_gene_id":"ENSG00000171812.12","gene_symbol":"COL8A2","gene_name":"collagen type VIII alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2216]","synonyms":"PPCD2,PPCD,FECD1,FECD","biotype":"protein_coding","ncbi_id":"1296","summary":"This gene encodes the alpha 2 chain of type VIII collagen. This protein is a major component of the basement membrane of the corneal endothelium and forms homo- or heterotrimers with alpha 1 (VIII) type collagens. Defects in this gene are associated with Fuchs endothelial corneal dystrophy and posterior polymorphous corneal dystrophy type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":36095236,"end":36125220,"strand":-1,"description":"collagen type VIII alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2216]"}, {"versioned_ensembl_gene_id":"ENSG00000111664.10","gene_symbol":"GNB3","gene_name":"G protein subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:4400]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2784","summary":"Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit which belongs to the WD repeat G protein beta family. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. A single-nucleotide polymorphism (C825T) in this gene is associated with essential hypertension and obesity. This polymorphism is also associated with the occurrence of the splice variant GNB3-s, which appears to have increased activity. GNB3-s is an example of alternative splicing caused by a nucleotide change outside of the splice donor and acceptor sites. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2014]","start":6839954,"end":6847393,"strand":1,"description":"G protein subunit beta 3 [Source:HGNC Symbol;Acc:HGNC:4400]"}, {"versioned_ensembl_gene_id":"ENSG00000107341.4","gene_symbol":"UBE2R2","gene_name":"ubiquitin conjugating enzyme E2 R2 [Source:HGNC Symbol;Acc:HGNC:19907]","synonyms":"UBC3B,MGC10481,FLJ20419,CDC34B","biotype":"protein_coding","ncbi_id":"54926","summary":"Protein kinase CK2 is a ubiquitous and pleiotropic Ser/Thr protein kinase involved in cell growth and transformation. This gene encodes a protein similar to the E2 ubiquitin conjugating enzyme UBC3/CDC34. Studies suggest that CK2-dependent phosphorylation of this ubiquitin-conjugating enzyme functions by regulating beta-TrCP substrate recognition and induces its interaction with beta-TrCP, enhancing beta-catenin degradation. [provided by RefSeq, Jul 2008]","start":33817567,"end":33920404,"strand":1,"description":"ubiquitin conjugating enzyme E2 R2 [Source:HGNC Symbol;Acc:HGNC:19907]"}, {"versioned_ensembl_gene_id":"ENSG00000101180.15","gene_symbol":"HRH3","gene_name":"histamine receptor H3 [Source:HGNC Symbol;Acc:HGNC:5184]","synonyms":"GPCR97","biotype":"protein_coding","ncbi_id":"11255","summary":"Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. Its various actions are mediated by histamine receptors H1, H2, H3 and H4. This gene encodes one of the histamine receptors (H3) which belongs to the family 1 of G protein-coupled receptors. It is an integral membrane protein and can regulate neurotransmitter release. This receptor can also increase voltage-dependent calcium current in smooth muscles and innervates the blood vessels and the heart in cardiovascular system. [provided by RefSeq, Jul 2008]","start":62214970,"end":62220267,"strand":-1,"description":"histamine receptor H3 [Source:HGNC Symbol;Acc:HGNC:5184]"}, {"versioned_ensembl_gene_id":"ENSG00000227301.1","gene_symbol":"AL356489.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33719690,"end":33722555,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234857.2","gene_symbol":"HNRNPUL2-BSCL2","gene_name":"HNRNPUL2-BSCL2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49189]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534595","summary":"This locus represents naturally occurring read-through transcription between the neighboring HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2) and BSCL2 (Berardinelli-Seip congenital lipodystrophy 2 (seipin)) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Mar 2011]","start":62690275,"end":62727384,"strand":-1,"description":"HNRNPUL2-BSCL2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49189]"}, {"versioned_ensembl_gene_id":"ENSG00000216901.1","gene_symbol":"ZNF603P","gene_name":"zinc finger protein 603, pseudogene [Source:HGNC Symbol;Acc:HGNC:23322]","synonyms":"p373c6.7","biotype":"unprocessed_pseudogene","ncbi_id":"493821","summary":null,"start":28176188,"end":28176674,"strand":1,"description":"zinc finger protein 603, pseudogene [Source:HGNC Symbol;Acc:HGNC:23322]"}, {"versioned_ensembl_gene_id":"ENSG00000227271.1","gene_symbol":"RPL39P25","gene_name":"ribosomal protein L39 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37002]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271517","summary":null,"start":75269392,"end":75269545,"strand":-1,"description":"ribosomal protein L39 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37002]"}, {"versioned_ensembl_gene_id":"ENSG00000268170.2","gene_symbol":"AC073342.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143220468,"end":143222267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162645.12","gene_symbol":"GBP2","gene_name":"guanylate binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4183]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2634","summary":"This gene belongs to the guanine-binding protein (GBP) family, which includes interferon-induced proteins that can bind to guanine nucleotides (GMP, GDP and GTP). The encoded protein is a GTPase which hydrolyzes GTP, predominantly to GDP. The protein may play a role as a marker of squamous cell carcinomas. [provided by RefSeq, Jul 2013]","start":89106132,"end":89150456,"strand":-1,"description":"guanylate binding protein 2 [Source:HGNC Symbol;Acc:HGNC:4183]"}, {"versioned_ensembl_gene_id":"ENSG00000272604.1","gene_symbol":"AC073073.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105571083,"end":105573660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101181.17","gene_symbol":"MTG2","gene_name":"mitochondrial ribosome associated GTPase 2 [Source:HGNC Symbol;Acc:HGNC:16239]","synonyms":"ObgH1,GTPBP5,FLJ10741,dJ1005F21.2","biotype":"protein_coding","ncbi_id":"26164","summary":"Small G proteins, such as GTPBP5, act as molecular switches that play crucial roles in the regulation of fundamental cellular processes such as protein synthesis, nuclear transport, membrane trafficking, and signal transduction (Hirano et al., 2006 [PubMed 17054726]).[supplied by OMIM, Mar 2008]","start":62183029,"end":62203568,"strand":1,"description":"mitochondrial ribosome associated GTPase 2 [Source:HGNC Symbol;Acc:HGNC:16239]"}, {"versioned_ensembl_gene_id":"ENSG00000274391.4","gene_symbol":"TPTE","gene_name":"transmembrane phosphatase with tensin homology [Source:HGNC Symbol;Acc:HGNC:12023]","synonyms":"PTEN2,CT44","biotype":"protein_coding","ncbi_id":"7179","summary":"This gene encodes a PTEN-related tyrosine phosphatase which may play a role in the signal transduction pathways of the endocrine or spermatogenic function of the testis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":10521553,"end":10606140,"strand":1,"description":"transmembrane phosphatase with tensin homology [Source:HGNC Symbol;Acc:HGNC:12023]"}, {"versioned_ensembl_gene_id":"ENSG00000267504.1","gene_symbol":"AC090236.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":58371566,"end":58372666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273076.1","gene_symbol":"AL021707.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38743495,"end":38743910,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250835.1","gene_symbol":"LSM3P4","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130178","summary":null,"start":142317238,"end":142317546,"strand":1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44349]"}, {"versioned_ensembl_gene_id":"ENSG00000163220.10","gene_symbol":"S100A9","gene_name":"S100 calcium binding protein A9 [Source:HGNC Symbol;Acc:HGNC:10499]","synonyms":"MAC387,LIAG,CGLB,CFAG,CAGB,60B8AG,P14,NIF,MRP14,MIF","biotype":"protein_coding","ncbi_id":"6280","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in the inhibition of casein kinase and altered expression of this protein is associated with the disease cystic fibrosis. This antimicrobial protein exhibits antifungal and antibacterial activity. [provided by RefSeq, Nov 2014]","start":153357854,"end":153361027,"strand":1,"description":"S100 calcium binding protein A9 [Source:HGNC Symbol;Acc:HGNC:10499]"}, {"versioned_ensembl_gene_id":"ENSG00000162069.14","gene_symbol":"BICDL2","gene_name":"BICD family like cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:33584]","synonyms":"CCDC64B","biotype":"protein_coding","ncbi_id":"146439","summary":null,"start":3027682,"end":3036926,"strand":-1,"description":"BICD family like cargo adaptor 2 [Source:HGNC Symbol;Acc:HGNC:33584]"}, {"versioned_ensembl_gene_id":"ENSG00000010165.19","gene_symbol":"METTL13","gene_name":"methyltransferase like 13 [Source:HGNC Symbol;Acc:HGNC:24248]","synonyms":"KIAA0859,CGI-01","biotype":"protein_coding","ncbi_id":"51603","summary":null,"start":171781664,"end":171814023,"strand":1,"description":"methyltransferase like 13 [Source:HGNC Symbol;Acc:HGNC:24248]"}, {"versioned_ensembl_gene_id":"ENSG00000177363.4","gene_symbol":"LRRN4CL","gene_name":"LRRN4 C-terminal like [Source:HGNC Symbol;Acc:HGNC:33724]","synonyms":null,"biotype":"protein_coding","ncbi_id":"221091","summary":null,"start":62686402,"end":62689899,"strand":-1,"description":"LRRN4 C-terminal like [Source:HGNC Symbol;Acc:HGNC:33724]"}, {"versioned_ensembl_gene_id":"ENSG00000212663.2","gene_symbol":"AC003035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13980066,"end":13988820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267722.1","gene_symbol":"AP002414.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12081540,"end":12085267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229827.1","gene_symbol":"AC093899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169577371,"end":169577746,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224866.1","gene_symbol":"USP9YP25","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:38761]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480715","summary":null,"start":23734193,"end":23736249,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:38761]"}, {"versioned_ensembl_gene_id":"ENSG00000233337.1","gene_symbol":"UBE2FP3","gene_name":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44537]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480360","summary":null,"start":111437514,"end":111438037,"strand":1,"description":"ubiquitin conjugating enzyme E2 F (putative) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44537]"}, {"versioned_ensembl_gene_id":"ENSG00000224954.1","gene_symbol":"BX248419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30177152,"end":30178961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260948.1","gene_symbol":"AL390195.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":111431046,"end":111433068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110851.11","gene_symbol":"PRDM4","gene_name":"PR/SET domain 4 [Source:HGNC Symbol;Acc:HGNC:9348]","synonyms":"PFM1","biotype":"protein_coding","ncbi_id":"11108","summary":"The protein encoded by this gene is a transcription factor of the PR-domain protein family. It contains a PR-domain and multiple zinc finger motifs. Transcription factors of the PR-domain family are known to be involved in cell differentiation and tumorigenesis. An elevated expression level of this gene has been observed in PC12 cells treated with nerve growth factor, beta polypeptide (NGF). This gene is located in a chromosomal region that is thought to contain tumor suppressor genes. [provided by RefSeq, Jul 2008]","start":107732866,"end":107761272,"strand":-1,"description":"PR/SET domain 4 [Source:HGNC Symbol;Acc:HGNC:9348]"}, {"versioned_ensembl_gene_id":"ENSG00000163218.14","gene_symbol":"PGLYRP4","gene_name":"peptidoglycan recognition protein 4 [Source:HGNC Symbol;Acc:HGNC:30015]","synonyms":"SBBI67,PGRPIB,PGRP-Ibeta,PGLYRPIbeta","biotype":"protein_coding","ncbi_id":"57115","summary":"Summary: This gene encodes a peptidoglycan recognition protein, which belongs to the N-acetylmuramoyl-L-alanine amidase 2 family. These proteins are part of the innate immune system and recognize peptidoglycan, a ubiquitous component of bacterial cell walls. This antimicrobial protein binds to murein peptidoglycans of Gram-positive bacteria. [provided by RefSeq, Oct 2014]","start":153330120,"end":153348840,"strand":-1,"description":"peptidoglycan recognition protein 4 [Source:HGNC Symbol;Acc:HGNC:30015]"}, {"versioned_ensembl_gene_id":"ENSG00000184602.5","gene_symbol":"SNN","gene_name":"stannin [Source:HGNC Symbol;Acc:HGNC:11149]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8303","summary":null,"start":11668414,"end":11679159,"strand":1,"description":"stannin [Source:HGNC Symbol;Acc:HGNC:11149]"}, {"versioned_ensembl_gene_id":"ENSG00000227228.1","gene_symbol":"UBDP1","gene_name":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]","synonyms":"dJ994E9.3","biotype":"unprocessed_pseudogene","ncbi_id":"100286971","summary":null,"start":29461167,"end":29466379,"strand":-1,"description":"ubiquitin D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18796]"}, {"versioned_ensembl_gene_id":"ENSG00000257683.1","gene_symbol":"LINC02463","gene_name":"long intergenic non-protein coding RNA 2463 [Source:HGNC Symbol;Acc:HGNC:53400]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370004","summary":null,"start":115810359,"end":115886137,"strand":-1,"description":"long intergenic non-protein coding RNA 2463 [Source:HGNC Symbol;Acc:HGNC:53400]"}, {"versioned_ensembl_gene_id":"ENSG00000137033.11","gene_symbol":"IL33","gene_name":"interleukin 33 [Source:HGNC Symbol;Acc:HGNC:16028]","synonyms":"DVS27,DKFZp586H0523,C9orf26,NF-HEV,IL1F11","biotype":"protein_coding","ncbi_id":"90865","summary":"The protein encoded by this gene is a cytokine that binds to the IL1RL1/ST2 receptor. The encoded protein is involved in the maturation of Th2 cells and the activation of mast cells, basophils, eosinophils and natural killer cells. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":6215786,"end":6257983,"strand":1,"description":"interleukin 33 [Source:HGNC Symbol;Acc:HGNC:16028]"}, {"versioned_ensembl_gene_id":"ENSG00000203783.4","gene_symbol":"PRR9","gene_name":"proline rich 9 [Source:HGNC Symbol;Acc:HGNC:32057]","synonyms":null,"biotype":"protein_coding","ncbi_id":"574414","summary":null,"start":153217584,"end":153219317,"strand":1,"description":"proline rich 9 [Source:HGNC Symbol;Acc:HGNC:32057]"}, {"versioned_ensembl_gene_id":"ENSG00000253390.1","gene_symbol":"AC104561.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23458601,"end":23484971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084733.10","gene_symbol":"RAB10","gene_name":"RAB10, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9759]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10890","summary":"RAB10 belongs to the RAS (see HRAS; MIM 190020) superfamily of small GTPases. RAB proteins localize to exocytic and endocytic compartments and regulate intracellular vesicle trafficking (Bao et al., 1998 [PubMed 9918381]).[supplied by OMIM, Mar 2009]","start":26034107,"end":26137454,"strand":1,"description":"RAB10, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9759]"}, {"versioned_ensembl_gene_id":"ENSG00000272324.5","gene_symbol":"AC012629.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10761065,"end":10770294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247809.7","gene_symbol":"NR2F2-AS1","gene_name":"NR2F2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44222]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"644192","summary":null,"start":96110040,"end":96327361,"strand":-1,"description":"NR2F2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44222]"}, {"versioned_ensembl_gene_id":"ENSG00000112234.8","gene_symbol":"FBXL4","gene_name":"F-box and leucine rich repeat protein 4 [Source:HGNC Symbol;Acc:HGNC:13601]","synonyms":"FBL5,FBL4","biotype":"protein_coding","ncbi_id":"26235","summary":"This gene encodes a member of the F-box protein family, which are characterized by an approximately 40 amino acid motif, the F-box. F-box proteins constitute one subunit of modular E3 ubiquitin ligase complexes, called SCF complexes, which function in phosphorylation-dependent ubiquitination. The F-box domain mediates protein-protein interactions and binds directly to S-phase kinase-associated protein 1. In addition to an F-box domain, the encoded protein contains at least 9 tandem leucine-rich repeats. The ubiquitin ligase complex containing the encoded protein may function in cell-cycle control by regulating levels of lysine-specific demethylase 4A. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":98868538,"end":98948006,"strand":-1,"description":"F-box and leucine rich repeat protein 4 [Source:HGNC Symbol;Acc:HGNC:13601]"}, {"versioned_ensembl_gene_id":"ENSG00000158769.17","gene_symbol":"F11R","gene_name":"F11 receptor [Source:HGNC Symbol;Acc:HGNC:14685]","synonyms":"PAM-1,JCAM,JAMA,JAM1,JAM-A,JAM-1,CD321","biotype":"protein_coding","ncbi_id":"50848","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. The protein encoded by this immunoglobulin superfamily gene member is an important regulator of tight junction assembly in epithelia. In addition, the encoded protein can act as (1) a receptor for reovirus, (2) a ligand for the integrin LFA1, involved in leukocyte transmigration, and (3) a platelet receptor. Multiple 5' alternatively spliced variants, encoding the same protein, have been identified but their biological validity has not been established. [provided by RefSeq, Jul 2008]","start":160995211,"end":161021348,"strand":-1,"description":"F11 receptor [Source:HGNC Symbol;Acc:HGNC:14685]"}, {"versioned_ensembl_gene_id":"ENSG00000230425.1","gene_symbol":"RSU1P1","gene_name":"Ras suppressor protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31114]","synonyms":"Y214H10.6","biotype":"unprocessed_pseudogene","ncbi_id":"100129622","summary":null,"start":42725857,"end":42737159,"strand":1,"description":"Ras suppressor protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31114]"}, {"versioned_ensembl_gene_id":"ENSG00000258108.1","gene_symbol":"AC009803.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115569664,"end":115581739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259966.5","gene_symbol":"AC137800.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32600299,"end":32615639,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231009.1","gene_symbol":"CUBNP1","gene_name":"cubilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44983]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728064","summary":null,"start":42694371,"end":42714575,"strand":-1,"description":"cubilin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44983]"}, {"versioned_ensembl_gene_id":"ENSG00000260922.1","gene_symbol":"AC009139.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77234877,"end":77290934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257726.1","gene_symbol":"AC078880.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":115363012,"end":115364745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234864.1","gene_symbol":"AL022344.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42696035,"end":42706453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163254.4","gene_symbol":"CRYGC","gene_name":"crystallin gamma C [Source:HGNC Symbol;Acc:HGNC:2410]","synonyms":"CRYG3","biotype":"protein_coding","ncbi_id":"1420","summary":"This gene encodes a member of the beta/gamma-crystallin family of proteins. Crystallins constitute the major proteins of vertebrate eye lens and maintain the transparency and refractive index of the lens. This gene and several family members are present in a gene cluster on chromosome 2. Mutations in this gene have been shown to cause multiple types of cataract, including Coppock-like cataract and zonular pulverulent cataract, among others. [provided by RefSeq, Jan 2015]","start":208128137,"end":208129830,"strand":-1,"description":"crystallin gamma C [Source:HGNC Symbol;Acc:HGNC:2410]"}, {"versioned_ensembl_gene_id":"ENSG00000261568.1","gene_symbol":"AL359694.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22220781,"end":22222395,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280443.1","gene_symbol":"AL136313.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21822536,"end":21822737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280620.1","gene_symbol":"AC012557.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63911518,"end":63911772,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158195.10","gene_symbol":"WASF2","gene_name":"WAS protein family member 2 [Source:HGNC Symbol;Acc:HGNC:12733]","synonyms":"WAVE2,SCAR2","biotype":"protein_coding","ncbi_id":"10163","summary":"This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location (PMID:10381382) has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":27404226,"end":27490158,"strand":-1,"description":"WAS protein family member 2 [Source:HGNC Symbol;Acc:HGNC:12733]"}, {"versioned_ensembl_gene_id":"ENSG00000182957.15","gene_symbol":"SPATA13","gene_name":"spermatogenesis associated 13 [Source:HGNC Symbol;Acc:HGNC:23222]","synonyms":"ARHGEF29,ARHGEF29,ASEF2,FLJ31208","biotype":"protein_coding","ncbi_id":"221178","summary":null,"start":23979805,"end":24307074,"strand":1,"description":"spermatogenesis associated 13 [Source:HGNC Symbol;Acc:HGNC:23222]"}, {"versioned_ensembl_gene_id":"ENSG00000227213.1","gene_symbol":"SPATA13-AS1","gene_name":"SPATA13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39905]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874231","summary":null,"start":24252749,"end":24254439,"strand":-1,"description":"SPATA13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39905]"}, {"versioned_ensembl_gene_id":"ENSG00000213958.2","gene_symbol":"KRT18P29","gene_name":"keratin 18 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:33398]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729050","summary":null,"start":181961212,"end":181962478,"strand":-1,"description":"keratin 18 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:33398]"}, {"versioned_ensembl_gene_id":"ENSG00000213782.7","gene_symbol":"DDX47","gene_name":"DEAD-box helicase 47 [Source:HGNC Symbol;Acc:HGNC:18682]","synonyms":"RRP3,HQ0256,FLJ30012,DKFZp564O176","biotype":"protein_coding","ncbi_id":"51202","summary":"This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene can shuttle between the nucleus and the cytoplasm, and has an RNA-independent ATPase activity. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":12813316,"end":12829981,"strand":1,"description":"DEAD-box helicase 47 [Source:HGNC Symbol;Acc:HGNC:18682]"}, {"versioned_ensembl_gene_id":"ENSG00000186951.16","gene_symbol":"PPARA","gene_name":"peroxisome proliferator activated receptor alpha [Source:HGNC Symbol;Acc:HGNC:9232]","synonyms":"PPAR,NR1C1,hPPAR","biotype":"protein_coding","ncbi_id":"5465","summary":"Peroxisome proliferators include hypolipidemic drugs, herbicides, leukotriene antagonists, and plasticizers; this term arises because they induce an increase in the size and number of peroxisomes. Peroxisomes are subcellular organelles found in plants and animals that contain enzymes for respiration and for cholesterol and lipid metabolism. The action of peroxisome proliferators is thought to be mediated via specific receptors, called PPARs, which belong to the steroid hormone receptor superfamily. PPARs affect the expression of target genes involved in cell proliferation, cell differentiation and in immune and inflammation responses. Three closely related subtypes (alpha, beta/delta, and gamma) have been identified. This gene encodes the subtype PPAR-alpha, which is a nuclear transcription factor. Multiple alternatively spliced transcript variants have been described for this gene, although the full-length nature of only two has been determined. [provided by RefSeq, Jul 2008]","start":46150521,"end":46243756,"strand":1,"description":"peroxisome proliferator activated receptor alpha [Source:HGNC Symbol;Acc:HGNC:9232]"}, {"versioned_ensembl_gene_id":"ENSG00000220643.1","gene_symbol":"AL031577.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34686602,"end":34687106,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258053.1","gene_symbol":"AC025575.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71047402,"end":71118247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278787.4","gene_symbol":"UBR7","gene_name":"ubiquitin protein ligase E3 component n-recognin 7 (putative) [Source:HGNC Symbol;Acc:HGNC:20344]","synonyms":"C14orf130","biotype":"protein_coding","ncbi_id":"55148","summary":"This gene encodes a UBR box-containing protein that belongs to the E3 ubiquitin ligase family. The protein also contains a plant homeodomain (PHD) in the C-terminus. In mammals, the encoded protein recognizes N-degrons, the destabilizing N-terminal residues of short-lived proteins, which results in ubiquitinylation, and proteolysis via the proteasome. [provided by RefSeq, Jul 2016]","start":93207056,"end":93229215,"strand":1,"description":"ubiquitin protein ligase E3 component n-recognin 7 (putative) [Source:HGNC Symbol;Acc:HGNC:20344]"}, {"versioned_ensembl_gene_id":"ENSG00000184697.6","gene_symbol":"CLDN6","gene_name":"claudin 6 [Source:HGNC Symbol;Acc:HGNC:2048]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9074","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. This gene encodes a component of tight junction strands, which is a member of the claudin family. The protein is an integral membrane protein and is one of the entry cofactors for hepatitis C virus. The gene methylation may be involved in esophageal tumorigenesis. This gene is adjacent to another family member CLDN9 on chromosome 16.[provided by RefSeq, Aug 2010]","start":3014712,"end":3020071,"strand":-1,"description":"claudin 6 [Source:HGNC Symbol;Acc:HGNC:2048]"}, {"versioned_ensembl_gene_id":"ENSG00000237629.1","gene_symbol":"UQCRHP2","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38045]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729769","summary":null,"start":25994794,"end":25995081,"strand":1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38045]"}, {"versioned_ensembl_gene_id":"ENSG00000224774.7","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb2,Ckb1","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31655985,"end":31664295,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000281141.1","gene_symbol":"AL110118.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93138066,"end":93138465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085465.12","gene_symbol":"OVGP1","gene_name":"oviductal glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:8524]","synonyms":"MUC9,CHIT5","biotype":"protein_coding","ncbi_id":"5016","summary":"This gene encodes a large, carbohydrate-rich, epithelial glycoprotein with numerous O-glycosylation sites located within threonine, serine, and proline-rich tandem repeats. The gene is similar to members of the mucin and the glycosyl hydrolase 18 gene families. Regulation of expression may be estrogen-dependent. Gene expression and protein secretion occur during late follicular development through early cleavage-stage embryonic development. The protein is secreted from non-ciliated oviductal epithelial cells and associates with ovulated oocytes, blastomeres, and spermatozoan acrosomal regions. [provided by RefSeq, Jul 2008]","start":111414314,"end":111427777,"strand":-1,"description":"oviductal glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:8524]"}, {"versioned_ensembl_gene_id":"ENSG00000256672.1","gene_symbol":"LINC02455","gene_name":"long intergenic non-protein coding RNA 2455 [Source:HGNC Symbol;Acc:HGNC:53388]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369597","summary":null,"start":674801,"end":684127,"strand":-1,"description":"long intergenic non-protein coding RNA 2455 [Source:HGNC Symbol;Acc:HGNC:53388]"}, {"versioned_ensembl_gene_id":"ENSG00000226823.1","gene_symbol":"SUGT1P1","gene_name":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19384]","synonyms":"SUGT1P,SGT1P,MGC15151,bA255A11.1","biotype":"unprocessed_pseudogene","ncbi_id":"441394","summary":null,"start":33503655,"end":33510711,"strand":-1,"description":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19384]"}, {"versioned_ensembl_gene_id":"ENSG00000262362.1","gene_symbol":"AC004233.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3003431,"end":3005101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229452.1","gene_symbol":"AC005162.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29080284,"end":29082527,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262268.3","gene_symbol":"OR9G3P","gene_name":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81159","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56751253,"end":56752170,"strand":1,"description":"olfactory receptor family 9 subfamily G member 3 pseudogene [Source:HGNC Symbol;Acc:HGNC:15321]"}, {"versioned_ensembl_gene_id":"ENSG00000220771.2","gene_symbol":"BOLA2P3","gene_name":"bolA family member 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51439]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480323","summary":null,"start":21602128,"end":21602383,"strand":1,"description":"bolA family member 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51439]"}, {"versioned_ensembl_gene_id":"ENSG00000213238.6","gene_symbol":"AC008155.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":138298088,"end":138298484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235400.1","gene_symbol":"AC104837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78749073,"end":78750659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230753.5","gene_symbol":"ZNF341-AS1","gene_name":"ZNF341 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50736]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929746","summary":null,"start":33787373,"end":33811097,"strand":-1,"description":"ZNF341 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50736]"}, {"versioned_ensembl_gene_id":"ENSG00000213104.3","gene_symbol":"NPM1P46","gene_name":"nucleophosmin 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45225]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729342","summary":null,"start":197379701,"end":197380892,"strand":-1,"description":"nucleophosmin 1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:45225]"}, {"versioned_ensembl_gene_id":"ENSG00000067066.16","gene_symbol":"SP100","gene_name":"SP100 nuclear antigen [Source:HGNC Symbol;Acc:HGNC:11206]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6672","summary":"This gene encodes a subnuclear organelle and major component of the PML (promyelocytic leukemia)-SP100 nuclear bodies. PML and SP100 are covalently modified by the SUMO-1 modifier, which is considered crucial to nuclear body interactions. The encoded protein binds heterochromatin proteins and is thought to play a role in tumorigenesis, immunity, and gene regulation. Alternatively spliced variants have been identified for this gene; one of which encodes a high-mobility group protein. [provided by RefSeq, Aug 2011]","start":230415942,"end":230544090,"strand":1,"description":"SP100 nuclear antigen [Source:HGNC Symbol;Acc:HGNC:11206]"}, {"versioned_ensembl_gene_id":"ENSG00000224611.1","gene_symbol":"AC007919.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":172522228,"end":172522444,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175040.5","gene_symbol":"CHST2","gene_name":"carbohydrate sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:1970]","synonyms":"C6ST","biotype":"protein_coding","ncbi_id":"9435","summary":"This locus encodes a sulfotransferase protein. The encoded enzyme catalyzes the sulfation of a nonreducing N-acetylglucosamine residue, and may play a role in biosynthesis of 6-sulfosialyl Lewis X antigen. [provided by RefSeq, Aug 2011]","start":143119331,"end":143124014,"strand":1,"description":"carbohydrate sulfotransferase 2 [Source:HGNC Symbol;Acc:HGNC:1970]"}, {"versioned_ensembl_gene_id":"ENSG00000257454.1","gene_symbol":"AC025575.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71034122,"end":71104526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254018.1","gene_symbol":"AC104036.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121884724,"end":121904273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132002.7","gene_symbol":"DNAJB1","gene_name":"DnaJ heat shock protein family (Hsp40) member B1 [Source:HGNC Symbol;Acc:HGNC:5270]","synonyms":"RSPH16B,HSPF1,Hsp40,Sis1","biotype":"protein_coding","ncbi_id":"3337","summary":"This gene encodes a member of the DnaJ or Hsp40 (heat shock protein 40 kD) family of proteins. DNAJ family members are characterized by a highly conserved amino acid stretch called the 'J-domain' and function as one of the two major classes of molecular chaperones involved in a wide range of cellular events, such as protein folding and oligomeric protein complex assembly. The encoded protein is a molecular chaperone that stimulates the ATPase activity of Hsp70 heat-shock proteins in order to promote protein folding and prevent misfolded protein aggregation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":14514770,"end":14529770,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B1 [Source:HGNC Symbol;Acc:HGNC:5270]"}, {"versioned_ensembl_gene_id":"ENSG00000172969.7","gene_symbol":"FRG2C","gene_name":"FSHD region gene 2 family member C [Source:HGNC Symbol;Acc:HGNC:33626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288801","summary":null,"start":75664330,"end":75667220,"strand":1,"description":"FSHD region gene 2 family member C [Source:HGNC Symbol;Acc:HGNC:33626]"}, {"versioned_ensembl_gene_id":"ENSG00000249200.1","gene_symbol":"AC110775.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154373886,"end":154374347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280241.3","gene_symbol":"AC079298.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154142122,"end":154298819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272779.1","gene_symbol":"AC245060.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22303224,"end":22310401,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234630.1","gene_symbol":"AC245060.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22293733,"end":22294794,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165406.15","gene_symbol":"MARCH8","gene_name":"membrane associated ring-CH-type finger 8 [Source:HGNC Symbol;Acc:HGNC:23356]","synonyms":"RNF178,MIR,MARCH-VIII,CMIR,c-MIR","biotype":"protein_coding","ncbi_id":"220972","summary":"MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010]","start":45454585,"end":45594906,"strand":-1,"description":"membrane associated ring-CH-type finger 8 [Source:HGNC Symbol;Acc:HGNC:23356]"}, {"versioned_ensembl_gene_id":"ENSG00000274367.1","gene_symbol":"AC004233.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2981175,"end":2981591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225111.1","gene_symbol":"AC083900.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":207868582,"end":207869915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115756.12","gene_symbol":"HPCAL1","gene_name":"hippocalcin like 1 [Source:HGNC Symbol;Acc:HGNC:5145]","synonyms":"BDR1,VILIP-3,HLP2","biotype":"protein_coding","ncbi_id":"3241","summary":"The protein encoded by this gene is a member of neuron-specific calcium-binding proteins family found in the retina and brain. It is highly similar to human hippocalcin protein and nearly identical to the rat and mouse hippocalcin like-1 proteins. It may be involved in the calcium-dependent regulation of rhodopsin phosphorylation and may be of relevance for neuronal signalling in the central nervous system. Several alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Apr 2012]","start":10302889,"end":10427617,"strand":1,"description":"hippocalcin like 1 [Source:HGNC Symbol;Acc:HGNC:5145]"}, {"versioned_ensembl_gene_id":"ENSG00000167775.10","gene_symbol":"CD320","gene_name":"CD320 molecule [Source:HGNC Symbol;Acc:HGNC:16692]","synonyms":"8D6A,8D6","biotype":"protein_coding","ncbi_id":"51293","summary":"This gene encodes the transcobalamin receptor that is expressed at the cell surface. It mediates the cellular uptake of transcobalamin bound cobalamin (vitamin B12), and is involved in B-cell proliferation and immunoglobulin secretion. Mutations in this gene are associated with methylmalonic aciduria. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]","start":8302127,"end":8308356,"strand":-1,"description":"CD320 molecule [Source:HGNC Symbol;Acc:HGNC:16692]"}, {"versioned_ensembl_gene_id":"ENSG00000249930.1","gene_symbol":"AC007016.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15492729,"end":15492972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226873.1","gene_symbol":"CDY14P","gene_name":"chromodomain protein Y-linked 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:23858]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386736","summary":null,"start":23674379,"end":23675392,"strand":1,"description":"chromodomain protein Y-linked 14 pseudogene [Source:HGNC Symbol;Acc:HGNC:23858]"}, {"versioned_ensembl_gene_id":"ENSG00000260478.1","gene_symbol":"AC007333.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52238082,"end":52269440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234020.1","gene_symbol":"CHIAP3","gene_name":"chitinase, acidic pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44464]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996315","summary":null,"start":111353275,"end":111367409,"strand":-1,"description":"chitinase, acidic pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44464]"}, {"versioned_ensembl_gene_id":"ENSG00000272211.1","gene_symbol":"AC114760.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":196151263,"end":196154881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156875.13","gene_symbol":"MFSD14A","gene_name":"major facilitator superfamily domain containing 14A [Source:HGNC Symbol;Acc:HGNC:23363]","synonyms":"HIAT1,DKFZP564L0864","biotype":"protein_coding","ncbi_id":"64645","summary":null,"start":100038097,"end":100083377,"strand":1,"description":"major facilitator superfamily domain containing 14A [Source:HGNC Symbol;Acc:HGNC:23363]"}, {"versioned_ensembl_gene_id":"ENSG00000150627.15","gene_symbol":"WDR17","gene_name":"WD repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:16661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116966","summary":"This gene encodes a WD repeat-containing protein. It is abundantly expressed in retina and testis, and is thought to be a candidate gene for retinal disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2009]","start":176065834,"end":176182818,"strand":1,"description":"WD repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:16661]"}, {"versioned_ensembl_gene_id":"ENSG00000157168.18","gene_symbol":"NRG1","gene_name":"neuregulin 1 [Source:HGNC Symbol;Acc:HGNC:7997]","synonyms":"NRG1-IT2,NDF,HRG,HGL,GGF","biotype":"protein_coding","ncbi_id":"3084","summary":"The protein encoded by this gene is a membrane glycoprotein that mediates cell-cell signaling and plays a critical role in the growth and development of multiple organ systems. An extraordinary variety of different isoforms are produced from this gene through alternative promoter usage and splicing. These isoforms are expressed in a tissue-specific manner and differ significantly in their structure, and are classified as types I, II, III, IV, V and VI. Dysregulation of this gene has been linked to diseases such as cancer, schizophrenia, and bipolar disorder (BPD). [provided by RefSeq, Apr 2016]","start":31639386,"end":32767959,"strand":1,"description":"neuregulin 1 [Source:HGNC Symbol;Acc:HGNC:7997]"}, {"versioned_ensembl_gene_id":"ENSG00000166145.14","gene_symbol":"SPINT1","gene_name":"serine peptidase inhibitor, Kunitz type 1 [Source:HGNC Symbol;Acc:HGNC:11246]","synonyms":"MANSC2,HAI","biotype":"protein_coding","ncbi_id":"6692","summary":"The protein encoded by this gene is a member of the Kunitz family of serine protease inhibitors. The protein is a potent inhibitor specific for HGF activator and is thought to be involved in the regulation of the proteolytic activation of HGF in injured tissues. Alternative splicing results in multiple variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":40844018,"end":40858207,"strand":1,"description":"serine peptidase inhibitor, Kunitz type 1 [Source:HGNC Symbol;Acc:HGNC:11246]"}, {"versioned_ensembl_gene_id":"ENSG00000228459.3","gene_symbol":"LINC01546","gene_name":"long intergenic non-protein coding RNA 1546 [Source:HGNC Symbol;Acc:HGNC:27336]","synonyms":"CXorf28","biotype":"lincRNA","ncbi_id":"100129464","summary":null,"start":3271820,"end":3284653,"strand":1,"description":"long intergenic non-protein coding RNA 1546 [Source:HGNC Symbol;Acc:HGNC:27336]"}, {"versioned_ensembl_gene_id":"ENSG00000166340.15","gene_symbol":"TPP1","gene_name":"tripeptidyl peptidase 1 [Source:HGNC Symbol;Acc:HGNC:2073]","synonyms":"SCAR7,CLN2","biotype":"protein_coding","ncbi_id":"1200","summary":"This gene encodes a member of the sedolisin family of serine proteases. The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity. It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification. Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis, which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome. [provided by RefSeq, Jul 2008]","start":6612763,"end":6619461,"strand":-1,"description":"tripeptidyl peptidase 1 [Source:HGNC Symbol;Acc:HGNC:2073]"}, {"versioned_ensembl_gene_id":"ENSG00000278304.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"CD158H,EB6ActII,EB6ActI,EB6ActI,CD158H,EB6ActII","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54860710,"end":54875253,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000237333.11","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31730753,"end":31753433,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000262927.1","gene_symbol":"FAM138D","gene_name":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]","synonyms":"F379,F379","biotype":"lincRNA","ncbi_id":"677784","summary":null,"start":36667,"end":38073,"strand":-1,"description":"family with sequence similarity 138 member D [Source:HGNC Symbol;Acc:HGNC:33583]"}, {"versioned_ensembl_gene_id":"ENSG00000173302.5","gene_symbol":"GPR148","gene_name":"G protein-coupled receptor 148 [Source:HGNC Symbol;Acc:HGNC:23623]","synonyms":"PGR6","biotype":"protein_coding","ncbi_id":"344561","summary":null,"start":130729070,"end":130730336,"strand":1,"description":"G protein-coupled receptor 148 [Source:HGNC Symbol;Acc:HGNC:23623]"}, {"versioned_ensembl_gene_id":"ENSG00000276527.1","gene_symbol":"AL356515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44684487,"end":44715393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230793.1","gene_symbol":"SMARCE1P5","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39734]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400129","summary":null,"start":44594858,"end":44596082,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39734]"}, {"versioned_ensembl_gene_id":"ENSG00000274803.4","gene_symbol":"BDP1","gene_name":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]","synonyms":"TFIIIB90,HSA238520,TFIIIB150,TFC5,TAF3B1,KIAA1689,TFNR,KIAA1241","biotype":"protein_coding","ncbi_id":"55814","summary":"The product of this gene is a subunit of the TFIIIB transcription initiation complex, which recruits RNA polymerase III to target promoters in order to initiate transcription. The encoded protein localizes to concentrated aggregates in the nucleus, and is required for transcription from all three types of polymerase III promoters. It is phosphorylated by casein kinase II during mitosis, resulting in its release from chromatin and suppression of polymerase III transcription. [provided by RefSeq, Jul 2008]","start":70780935,"end":70893131,"strand":1,"description":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]"}, {"versioned_ensembl_gene_id":"ENSG00000136270.13","gene_symbol":"TBRG4","gene_name":"transforming growth factor beta regulator 4 [Source:HGNC Symbol;Acc:HGNC:17443]","synonyms":"KIAA0948,H_TD2522F11.8,FASTKD4,Cpr2","biotype":"protein_coding","ncbi_id":"9238","summary":null,"start":45100100,"end":45112047,"strand":-1,"description":"transforming growth factor beta regulator 4 [Source:HGNC Symbol;Acc:HGNC:17443]"}, {"versioned_ensembl_gene_id":"ENSG00000174495.12","gene_symbol":"AC005017.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28279211,"end":28279700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146263.11","gene_symbol":"MMS22L","gene_name":"MMS22 like, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:21475]","synonyms":"dJ39B17.2,C6orf167","biotype":"protein_coding","ncbi_id":"253714","summary":"The protein encoded by this gene forms a complex with tonsoku-like, DNA repair protein (TONSL), and this complex recognizes and repairs DNA double-strand breaks at sites of stalled or collapsed replication forks. The encoded protein also can bind with the histone-associated protein NFKBIL2 to help regulate the chromatin state at stalled replication forks. Finally, this gene appears to be overexpressed in most lung and esophageal cancers. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2017]","start":97142161,"end":97283217,"strand":-1,"description":"MMS22 like, DNA repair protein [Source:HGNC Symbol;Acc:HGNC:21475]"}, {"versioned_ensembl_gene_id":"ENSG00000112242.14","gene_symbol":"E2F3","gene_name":"E2F transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:3115]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1871","summary":"This gene encodes a member of a small family of transcription factors that function through binding of DP interaction partner proteins. The encoded protein recognizes a specific sequence motif in DNA and interacts directly with the retinoblastoma protein (pRB) to regulate the expression of genes involved in the cell cycle. Altered copy number and activity of this gene have been observed in a number of human cancers. There are pseudogenes for this gene on chromosomes 2 and 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]","start":20401906,"end":20493715,"strand":1,"description":"E2F transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:3115]"}, {"versioned_ensembl_gene_id":"ENSG00000273145.1","gene_symbol":"BX537318.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46013606,"end":46015498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224465.1","gene_symbol":"SOCS2P2","gene_name":"suppressor of cytokine signaling 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19330]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"266701","summary":null,"start":22170983,"end":22171556,"strand":-1,"description":"suppressor of cytokine signaling 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:19330]"}, {"versioned_ensembl_gene_id":"ENSG00000211637.2","gene_symbol":"IGLV4-69","gene_name":"immunoglobulin lambda variable 4-69 [Source:HGNC Symbol;Acc:HGNC:5921]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28784","summary":null,"start":22030934,"end":22031472,"strand":1,"description":"immunoglobulin lambda variable 4-69 [Source:HGNC Symbol;Acc:HGNC:5921]"}, {"versioned_ensembl_gene_id":"ENSG00000211641.3","gene_symbol":"IGLV11-55","gene_name":"immunoglobulin lambda variable 11-55 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5886]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28770","summary":null,"start":22201663,"end":22202161,"strand":1,"description":"immunoglobulin lambda variable 11-55 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5886]"}, {"versioned_ensembl_gene_id":"ENSG00000253242.1","gene_symbol":"IGLVIV-64","gene_name":"immunoglobulin lambda variable (IV)-64 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5943]","synonyms":"IGLV(IV)-64","biotype":"IG_V_pseudogene","ncbi_id":"28760","summary":null,"start":22075366,"end":22075666,"strand":1,"description":"immunoglobulin lambda variable (IV)-64 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5943]"}, {"versioned_ensembl_gene_id":"ENSG00000273125.1","gene_symbol":"LINC01990","gene_name":"long intergenic non-protein coding RNA 1990 [Source:HGNC Symbol;Acc:HGNC:52822]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929607","summary":null,"start":107430930,"end":107463912,"strand":1,"description":"long intergenic non-protein coding RNA 1990 [Source:HGNC Symbol;Acc:HGNC:52822]"}, {"versioned_ensembl_gene_id":"ENSG00000272097.1","gene_symbol":"AL024498.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10743324,"end":10747663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255095.2","gene_symbol":"OR1D4","gene_name":"olfactory receptor family 1 subfamily D member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8185]","synonyms":"OR17-30","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653166","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":3235703,"end":3241614,"strand":1,"description":"olfactory receptor family 1 subfamily D member 4 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8185]"}, {"versioned_ensembl_gene_id":"ENSG00000282592.1","gene_symbol":"IGHD1-20","gene_name":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]","synonyms":"IGHD120","biotype":"IG_D_gene","ncbi_id":"28507","summary":null,"start":105891962,"end":105891978,"strand":-1,"description":"immunoglobulin heavy diversity 1-20 [Source:HGNC Symbol;Acc:HGNC:5484]"}, {"versioned_ensembl_gene_id":"ENSG00000282274.1","gene_symbol":"IGHD4-17","gene_name":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]","synonyms":"IGHD417","biotype":"IG_D_gene","ncbi_id":"28494","summary":null,"start":105895279,"end":105895294,"strand":-1,"description":"immunoglobulin heavy diversity 4-17 [Source:HGNC Symbol;Acc:HGNC:5503]"}, {"versioned_ensembl_gene_id":"ENSG00000261610.1","gene_symbol":"AP000265.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32259804,"end":32261585,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281174.1","gene_symbol":"AC226496.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68743709,"end":68743987,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279502.1","gene_symbol":"AC016542.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":72756398,"end":72757016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189037.7","gene_symbol":"DUSP21","gene_name":"dual specificity phosphatase 21 [Source:HGNC Symbol;Acc:HGNC:20476]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63904","summary":"This gene encodes a member of the dual specificity phosphatase family, specifically the low molecular weight dual specificity phosphatase family. The encoded protein localizes to both the cytoplasm and the nucleus and functions to remove phosphate groups from phosphotyrosine and phosphothreonine residues.[provided by RefSeq, Mar 2009]","start":44844004,"end":44844888,"strand":1,"description":"dual specificity phosphatase 21 [Source:HGNC Symbol;Acc:HGNC:20476]"}, {"versioned_ensembl_gene_id":"ENSG00000073067.13","gene_symbol":"CYP2W1","gene_name":"cytochrome P450 family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:20243]","synonyms":"MGC34287,FLJ20359","biotype":"protein_coding","ncbi_id":"54905","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. [provided by RefSeq, Jul 2008]","start":983199,"end":989640,"strand":1,"description":"cytochrome P450 family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:20243]"}, {"versioned_ensembl_gene_id":"ENSG00000164741.14","gene_symbol":"DLC1","gene_name":"DLC1 Rho GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:2897]","synonyms":"STARD12,p122-RhoGAP,HP,DLC-1,ARHGAP7","biotype":"protein_coding","ncbi_id":"10395","summary":"This gene encodes a GTPase-activating protein (GAP) that is a member of the rhoGAP family of proteins which play a role in the regulation of small GTP-binding proteins. GAP family proteins participate in signaling pathways that regulate cell processes involved in cytoskeletal changes. This gene functions as a tumor suppressor gene in a number of common cancers, including prostate, lung, colorectal, and breast cancers. Multiple transcript variants due to alternative promoters and alternative splicing have been found for this gene.[provided by RefSeq, Apr 2010]","start":13083361,"end":13604610,"strand":-1,"description":"DLC1 Rho GTPase activating protein [Source:HGNC Symbol;Acc:HGNC:2897]"}, {"versioned_ensembl_gene_id":"ENSG00000111885.6","gene_symbol":"MAN1A1","gene_name":"mannosidase alpha class 1A member 1 [Source:HGNC Symbol;Acc:HGNC:6821]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4121","summary":"This gene encodes a class I mammalian Golgi 1,2-mannosidase which is a type II transmembrane protein. This protein catalyzes the hydrolysis of three terminal mannose residues from peptide-bound Man(9)-GlcNAc(2) oligosaccharides and belongs to family 47 of glycosyl hydrolases. [provided by RefSeq, Jul 2012]","start":119177209,"end":119349761,"strand":-1,"description":"mannosidase alpha class 1A member 1 [Source:HGNC Symbol;Acc:HGNC:6821]"}, {"versioned_ensembl_gene_id":"ENSG00000214016.3","gene_symbol":"RPSAP61","gene_name":"ribosomal protein SA pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:36760]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644464","summary":null,"start":44741087,"end":44741964,"strand":1,"description":"ribosomal protein SA pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:36760]"}, {"versioned_ensembl_gene_id":"ENSG00000234676.1","gene_symbol":"IFT74-AS1","gene_name":"IFT74 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49806]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929602","summary":null,"start":26955780,"end":26956295,"strand":-1,"description":"IFT74 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49806]"}, {"versioned_ensembl_gene_id":"ENSG00000233543.1","gene_symbol":"CHTF8P1","gene_name":"chromosome transmission fidelity factor 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35443]","synonyms":"CHTF8P","biotype":"processed_pseudogene","ncbi_id":"677883","summary":null,"start":44633692,"end":44635232,"strand":1,"description":"chromosome transmission fidelity factor 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35443]"}, {"versioned_ensembl_gene_id":"ENSG00000077782.19","gene_symbol":"FGFR1","gene_name":"fibroblast growth factor receptor 1 [Source:HGNC Symbol;Acc:HGNC:3688]","synonyms":"H3,H2,FLT2,FLG,CEK,N-SAM,CD331,KAL2,BFGFR,H5,H4","biotype":"protein_coding","ncbi_id":"2260","summary":"The protein encoded by this gene is a member of the fibroblast growth factor receptor (FGFR) family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member binds both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations in this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal aberrations involving this gene are associated with stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]","start":38411138,"end":38468834,"strand":-1,"description":"fibroblast growth factor receptor 1 [Source:HGNC Symbol;Acc:HGNC:3688]"}, {"versioned_ensembl_gene_id":"ENSG00000280740.1","gene_symbol":"AC226496.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68667002,"end":68669858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149798.4","gene_symbol":"CDC42EP2","gene_name":"CDC42 effector protein 2 [Source:HGNC Symbol;Acc:HGNC:16263]","synonyms":"CEP2,BORG1","biotype":"protein_coding","ncbi_id":"10435","summary":"CDC42, a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to, and negatively regulate the function of CDC42. Coexpression of this protein with CDC42 suggested a role of this protein in actin filament assembly and cell shape control. [provided by RefSeq, Aug 2011]","start":65314818,"end":65322429,"strand":1,"description":"CDC42 effector protein 2 [Source:HGNC Symbol;Acc:HGNC:16263]"}, {"versioned_ensembl_gene_id":"ENSG00000232799.1","gene_symbol":"CRYGFP","gene_name":"crystallin gamma F, pseudogene [Source:HGNC Symbol;Acc:HGNC:2413]","synonyms":"p1,CRYGFP1,CRYG6","biotype":"unprocessed_pseudogene","ncbi_id":"1423","summary":null,"start":209145241,"end":209147687,"strand":1,"description":"crystallin gamma F, pseudogene [Source:HGNC Symbol;Acc:HGNC:2413]"}, {"versioned_ensembl_gene_id":"ENSG00000197283.15","gene_symbol":"SYNGAP1","gene_name":"synaptic Ras GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:11497]","synonyms":"KIAA1938,SYNGAP,RASA5","biotype":"protein_coding","ncbi_id":"8831","summary":"This gene encodes a Ras GTPase activating protein that is a member of the N-methyl-D-aspartate receptor complex. The N-terminal domain of the protein contains a Ras-GAP domain, a pleckstrin homology domain, and a C2 domain that may be involved in binding of calcium and phospholipids. The C-terminal domain consists of a ten histidine repeat region, serine and tyrosine phosphorylation sites, and a T/SXV motif required for postsynaptic scaffold protein interaction. The encoded protein negatively regulates Ras, Rap and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking to the postsynaptic membrane to regulate synaptic plasticity and neuronal homeostasis. Allelic variants of this gene are associated with intellectual disability and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":33419661,"end":33457541,"strand":1,"description":"synaptic Ras GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:11497]"}, {"versioned_ensembl_gene_id":"ENSG00000058085.14","gene_symbol":"LAMC2","gene_name":"laminin subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:6493]","synonyms":"nicein-100kDa,LAMNB2,LAMB2T,kalinin-105kDa,EBR2A,EBR2,BM600-100kDa","biotype":"protein_coding","ncbi_id":"3918","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins, composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively), have a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the gamma chain isoform laminin, gamma 2. The gamma 2 chain, formerly thought to be a truncated version of beta chain (B2t), is highly homologous to the gamma 1 chain; however, it lacks domain VI, and domains V, IV and III are shorter. It is expressed in several fetal tissues but differently from gamma 1, and is specifically localized to epithelial cells in skin, lung and kidney. The gamma 2 chain together with alpha 3 and beta 3 chains constitute laminin 5 (earlier known as kalinin), which is an integral part of the anchoring filaments that connect epithelial cells to the underlying basement membrane. The epithelium-specific expression of the gamma 2 chain implied its role as an epithelium attachment molecule, and mutations in this gene have been associated with junctional epidermolysis bullosa, a skin disease characterized by blisters due to disruption of the epidermal-dermal junction. Two transcript variants resulting from alternative splicing of the 3' terminal exon, and encoding different isoforms of gamma 2 chain, have been described. The two variants are differentially expressed in embryonic tissues, however, the biological significance of the two forms is not known. Transcript variants utilizing alternative polyA_signal have also been noted in literature. [provided by RefSeq, Aug 2011]","start":183186238,"end":183244900,"strand":1,"description":"laminin subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:6493]"}, {"versioned_ensembl_gene_id":"ENSG00000105778.18","gene_symbol":"AVL9","gene_name":"AVL9 cell migration associated [Source:HGNC Symbol;Acc:HGNC:28994]","synonyms":"KIAA0241","biotype":"protein_coding","ncbi_id":"23080","summary":null,"start":32495426,"end":32588721,"strand":1,"description":"AVL9 cell migration associated [Source:HGNC Symbol;Acc:HGNC:28994]"}, {"versioned_ensembl_gene_id":"ENSG00000182885.16","gene_symbol":"ADGRG3","gene_name":"adhesion G protein-coupled receptor G3 [Source:HGNC Symbol;Acc:HGNC:13728]","synonyms":"PGR26,Pb99,GPR97","biotype":"protein_coding","ncbi_id":"222487","summary":null,"start":57668187,"end":57689378,"strand":1,"description":"adhesion G protein-coupled receptor G3 [Source:HGNC Symbol;Acc:HGNC:13728]"}, {"versioned_ensembl_gene_id":"ENSG00000227573.2","gene_symbol":"AC004986.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":122849746,"end":122850352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251441.2","gene_symbol":"RTEL1P1","gene_name":"regulator of telomere elongation helicase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44213]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421429","summary":null,"start":112356135,"end":112359819,"strand":1,"description":"regulator of telomere elongation helicase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44213]"}, {"versioned_ensembl_gene_id":"ENSG00000162694.13","gene_symbol":"EXTL2","gene_name":"exostosin like glycosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:3516]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2135","summary":null,"start":100872372,"end":100895998,"strand":-1,"description":"exostosin like glycosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:3516]"}, {"versioned_ensembl_gene_id":"ENSG00000197361.7","gene_symbol":"FBXL22","gene_name":"F-box and leucine rich repeat protein 22 [Source:HGNC Symbol;Acc:HGNC:27537]","synonyms":"FLJ39626,Fbl22","biotype":"protein_coding","ncbi_id":"283807","summary":"This gene encodes a member of the F-box protein family. This F-box protein interacts with S-phase kinase-associated protein 1A and cullin in order to form SCF complexes which function as ubiquitin ligases.[provided by RefSeq, Sep 2010]","start":63597353,"end":63602428,"strand":1,"description":"F-box and leucine rich repeat protein 22 [Source:HGNC Symbol;Acc:HGNC:27537]"}, {"versioned_ensembl_gene_id":"ENSG00000151025.9","gene_symbol":"GPR158","gene_name":"G protein-coupled receptor 158 [Source:HGNC Symbol;Acc:HGNC:23689]","synonyms":"KIAA1136","biotype":"protein_coding","ncbi_id":"57512","summary":null,"start":25175062,"end":25602226,"strand":1,"description":"G protein-coupled receptor 158 [Source:HGNC Symbol;Acc:HGNC:23689]"}, {"versioned_ensembl_gene_id":"ENSG00000231422.2","gene_symbol":"LINC01516","gene_name":"long intergenic non-protein coding RNA 1516 [Source:HGNC Symbol;Acc:HGNC:51211]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929025","summary":null,"start":25113058,"end":25161236,"strand":1,"description":"long intergenic non-protein coding RNA 1516 [Source:HGNC Symbol;Acc:HGNC:51211]"}, {"versioned_ensembl_gene_id":"ENSG00000104756.15","gene_symbol":"KCTD9","gene_name":"potassium channel tetramerization domain containing 9 [Source:HGNC Symbol;Acc:HGNC:22401]","synonyms":"FLJ20038,BTBD27","biotype":"protein_coding","ncbi_id":"54793","summary":null,"start":25427847,"end":25458476,"strand":-1,"description":"potassium channel tetramerization domain containing 9 [Source:HGNC Symbol;Acc:HGNC:22401]"}, {"versioned_ensembl_gene_id":"ENSG00000158006.13","gene_symbol":"PAFAH2","gene_name":"platelet activating factor acetylhydrolase 2 [Source:HGNC Symbol;Acc:HGNC:8579]","synonyms":"HSD-PLA2","biotype":"protein_coding","ncbi_id":"5051","summary":"This gene encodes platelet-activating factor acetylhydrolase isoform 2, a single-subunit intracellular enzyme that catalyzes the removal of the acetyl group at the SN-2 position of platelet-activating factor (identified as 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine). However, this lipase exhibits a broader substrate specificity than simply platelet activating factor. Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist, and both are multi-subunit enzymes. Additionally, there is a single-subunit serum isoform of this enzyme. [provided by RefSeq, Jul 2008]","start":25959767,"end":25998157,"strand":-1,"description":"platelet activating factor acetylhydrolase 2 [Source:HGNC Symbol;Acc:HGNC:8579]"}, {"versioned_ensembl_gene_id":"ENSG00000230926.1","gene_symbol":"AC239367.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":51082818,"end":51091228,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273765.1","gene_symbol":"AC024257.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48360920,"end":48361377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248881.1","gene_symbol":"AC010245.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75598482,"end":75599380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146700.8","gene_symbol":"SSC4D","gene_name":"scavenger receptor cysteine rich family member with 4 domains [Source:HGNC Symbol;Acc:HGNC:14461]","synonyms":"SRCRB4D,SRCRB-S4D,S4D-SRCRB","biotype":"protein_coding","ncbi_id":"136853","summary":"The scavenger receptor cysteine-rich (SRCR) superfamily is an ancient and highly conserved group of cell surface and/or secreted proteins, some of which are involved in the development of the immune system and the regulation of both innate and adaptive immune responses. Group B SRCR domains usually contain 8 regularly spaced cysteines that give rise to a well-defined intradomain disulfide-bond pattern.[supplied by OMIM, Apr 2004]","start":76389334,"end":76409695,"strand":-1,"description":"scavenger receptor cysteine rich family member with 4 domains [Source:HGNC Symbol;Acc:HGNC:14461]"}, {"versioned_ensembl_gene_id":"ENSG00000152766.5","gene_symbol":"ANKRD22","gene_name":"ankyrin repeat domain 22 [Source:HGNC Symbol;Acc:HGNC:28321]","synonyms":"MGC22805","biotype":"protein_coding","ncbi_id":"118932","summary":null,"start":88822132,"end":88851818,"strand":-1,"description":"ankyrin repeat domain 22 [Source:HGNC Symbol;Acc:HGNC:28321]"}, {"versioned_ensembl_gene_id":"ENSG00000283456.1","gene_symbol":"MTND1P37","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:52314]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729170","summary":null,"start":19747172,"end":19747435,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:52314]"}, {"versioned_ensembl_gene_id":"ENSG00000279041.1","gene_symbol":"AC102945.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30552345,"end":30553766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158571.10","gene_symbol":"PFKFB1","gene_name":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:8872]","synonyms":"PFRX","biotype":"protein_coding","ncbi_id":"5207","summary":"This gene encodes a member of the family of bifunctional 6-phosphofructo-2-kinase:fructose-2,6-biphosphatase enzymes. The enzyme forms a homodimer that catalyzes both the synthesis and degradation of fructose-2,6-biphosphate using independent catalytic domains. Fructose-2,6-biphosphate is an activator of the glycolysis pathway and an inhibitor of the gluconeogenesis pathway. Consequently, regulating fructose-2,6-biphosphate levels through the activity of this enzyme is thought to regulate glucose homeostasis. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2012]","start":54932961,"end":54998534,"strand":-1,"description":"6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:8872]"}, {"versioned_ensembl_gene_id":"ENSG00000226405.1","gene_symbol":"AL133325.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21488244,"end":21488625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282496.1","gene_symbol":"AF252830.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7410936,"end":7412491,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278908.1","gene_symbol":"AC132154.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30677762,"end":30679895,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274195.2","gene_symbol":"ZNF705G","gene_name":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100131980","summary":null,"start":7348669,"end":7377169,"strand":-1,"description":"zinc finger protein 705G [Source:HGNC Symbol;Acc:HGNC:37134]"}, {"versioned_ensembl_gene_id":"ENSG00000227544.8","gene_symbol":"AC018647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35715034,"end":35734887,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257368.2","gene_symbol":"AC063924.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45444766,"end":45445438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229068.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"TMPOL1,Em:AB014080.3","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30466452,"end":30467994,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000182415.9","gene_symbol":"CDY2A","gene_name":"chromodomain Y-linked 2A [Source:HGNC Symbol;Acc:HGNC:1810]","synonyms":"CDY2","biotype":"protein_coding","ncbi_id":"9426","summary":"This intronless gene encodes a protein containing a chromodomain and a histone acetyltransferase catalytic domain. Chromodomain proteins are components of heterochromatin-like complexes and can act as gene repressors. This protein is localized to the nucleus of late spermatids where histone hyperacetylation takes place. Histone hyperacetylation is thought to facilitate the transition in which protamines replace histones as the major DNA-packaging protein. Two nearly identical copies of this gene are found in a palindromic region on chromosome Y; this record represents the telomeric copy. Chromosome Y also contains a pair of closely related genes in another more telomeric palindrome as well as several related pseudogenes. [provided by RefSeq, Jul 2008]","start":18025787,"end":18028597,"strand":1,"description":"chromodomain Y-linked 2A [Source:HGNC Symbol;Acc:HGNC:1810]"}, {"versioned_ensembl_gene_id":"ENSG00000168028.13","gene_symbol":"RPSA","gene_name":"ribosomal protein SA [Source:HGNC Symbol;Acc:HGNC:6502]","synonyms":"SA,p40,LRP,LAMR1,37LRP","biotype":"protein_coding","ncbi_id":"3921","summary":"Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Many of the effects of laminin are mediated through interactions with cell surface receptors. These receptors include members of the integrin family, as well as non-integrin laminin-binding proteins. This gene encodes a high-affinity, non-integrin family, laminin receptor 1. This receptor has been variously called 67 kD laminin receptor, 37 kD laminin receptor precursor (37LRP) and p40 ribosome-associated protein. The amino acid sequence of laminin receptor 1 is highly conserved through evolution, suggesting a key biological function. It has been observed that the level of the laminin receptor transcript is higher in colon carcinoma tissue and lung cancer cell line than their normal counterparts. Also, there is a correlation between the upregulation of this polypeptide in cancer cells and their invasive and metastatic phenotype. Multiple copies of this gene exist, however, most of them are pseudogenes thought to have arisen from retropositional events. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":39406689,"end":39412542,"strand":1,"description":"ribosomal protein SA [Source:HGNC Symbol;Acc:HGNC:6502]"}, {"versioned_ensembl_gene_id":"ENSG00000088340.15","gene_symbol":"FER1L4","gene_name":"fer-1 like family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:15801]","synonyms":"dJ309K20.1,C20orf124,bA563A22B.1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"80307","summary":null,"start":35558737,"end":35607562,"strand":-1,"description":"fer-1 like family member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:15801]"}, {"versioned_ensembl_gene_id":"ENSG00000231105.1","gene_symbol":"AL031728.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21293290,"end":21299774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239503.1","gene_symbol":"MARK2P8","gene_name":"microtubule affinity regulating kinase 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421498","summary":null,"start":128748538,"end":128749489,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39799]"}, {"versioned_ensembl_gene_id":"ENSG00000239483.1","gene_symbol":"AC023598.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128798841,"end":128799201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242992.3","gene_symbol":"FTH1P4","gene_name":"ferritin heavy chain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3991]","synonyms":"FTHL4","biotype":"processed_pseudogene","ncbi_id":"2499","summary":null,"start":128764466,"end":128765018,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3991]"}, {"versioned_ensembl_gene_id":"ENSG00000273707.4","gene_symbol":"CDKN1C","gene_name":"cyclin dependent kinase inhibitor 1C [Source:HGNC Symbol;Acc:HGNC:1786]","synonyms":"BWS,BWCR,P57,KIP2","biotype":"protein_coding","ncbi_id":"1028","summary":"This gene is imprinted, with preferential expression of the maternal allele. The encoded protein is a tight-binding, strong inhibitor of several G1 cyclin/Cdk complexes and a negative regulator of cell proliferation. Mutations in this gene are implicated in sporadic cancers and Beckwith-Wiedemann syndorome, suggesting that this gene is a tumor suppressor candidate. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]","start":2883205,"end":2885904,"strand":-1,"description":"cyclin dependent kinase inhibitor 1C [Source:HGNC Symbol;Acc:HGNC:1786]"}, {"versioned_ensembl_gene_id":"ENSG00000014138.8","gene_symbol":"POLA2","gene_name":"DNA polymerase alpha 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:30073]","synonyms":"FLJ21662","biotype":"protein_coding","ncbi_id":"23649","summary":null,"start":65261762,"end":65305589,"strand":1,"description":"DNA polymerase alpha 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:30073]"}, {"versioned_ensembl_gene_id":"ENSG00000278062.2","gene_symbol":"ZNF251","gene_name":"zinc finger protein 251 [Source:HGNC Symbol;Acc:HGNC:13045]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90987","summary":null,"start":144724139,"end":144759649,"strand":-1,"description":"zinc finger protein 251 [Source:HGNC Symbol;Acc:HGNC:13045]"}, {"versioned_ensembl_gene_id":"ENSG00000147872.9","gene_symbol":"PLIN2","gene_name":"perilipin 2 [Source:HGNC Symbol;Acc:HGNC:248]","synonyms":"ADRP,ADFP","biotype":"protein_coding","ncbi_id":"123","summary":"The protein encoded by this gene belongs to the perilipin family, members of which coat intracellular lipid storage droplets. This protein is associated with the lipid globule surface membrane material, and maybe involved in development and maintenance of adipose tissue. However, it is not restricted to adipocytes as previously thought, but is found in a wide range of cultured cell lines, including fibroblasts, endothelial and epithelial cells, and tissues, such as lactating mammary gland, adrenal cortex, Sertoli and Leydig cells, and hepatocytes in alcoholic liver cirrhosis, suggesting that it may serve as a marker of lipid accumulation in diverse cell types and diseases. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2011]","start":19108375,"end":19149290,"strand":-1,"description":"perilipin 2 [Source:HGNC Symbol;Acc:HGNC:248]"}, {"versioned_ensembl_gene_id":"ENSG00000282778.1","gene_symbol":"IGHJ2P","gene_name":"immunoglobulin heavy joining 2P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5535]","synonyms":"Jpsi2","biotype":"IG_J_pseudogene","ncbi_id":"28480","summary":null,"start":105865564,"end":105865623,"strand":-1,"description":"immunoglobulin heavy joining 2P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5535]"}, {"versioned_ensembl_gene_id":"ENSG00000170027.6","gene_symbol":"YWHAG","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma [Source:HGNC Symbol;Acc:HGNC:12852]","synonyms":"PPP1R170","biotype":"protein_coding","ncbi_id":"7532","summary":"This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both plants and mammals, and this protein is 100% identical to the rat ortholog. It is induced by growth factors in human vascular smooth muscle cells, and is also highly expressed in skeletal and heart muscles, suggesting an important role for this protein in muscle tissue. It has been shown to interact with RAF1 and protein kinase C, proteins involved in various signal transduction pathways. [provided by RefSeq, Jul 2008]","start":76326794,"end":76359031,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma [Source:HGNC Symbol;Acc:HGNC:12852]"}, {"versioned_ensembl_gene_id":"ENSG00000117281.15","gene_symbol":"CD160","gene_name":"CD160 molecule [Source:HGNC Symbol;Acc:HGNC:17013]","synonyms":"NK28,NK1,BY55","biotype":"protein_coding","ncbi_id":"11126","summary":"CD160 is an 27 kDa glycoprotein which was initially identified with the monoclonal antibody BY55. Its expression is tightly associated with peripheral blood NK cells and CD8 T lymphocytes with cytolytic effector activity. The cDNA sequence of CD160 predicts a cysteine-rich, glycosylphosphatidylinositol-anchored protein of 181 amino acids with a single Ig-like domain weakly homologous to KIR2DL4 molecule. CD160 is expressed at the cell surface as a tightly disulfide-linked multimer. RNA blot analysis revealed CD160 mRNAs of 1.5 and 1.6 kb whose expression was highly restricted to circulating NK and T cells, spleen and small intestine. Within NK cells CD160 is expressed by CD56dimCD16+ cells whereas among circulating T cells its expression is mainly restricted to TCRgd bearing cells and to TCRab+CD8brightCD95+CD56+CD28-CD27-cells. In tissues, CD160 is expressed on all intestinal intraepithelial lymphocytes. CD160 shows a broad specificity for binding to both classical and nonclassical MHC class I molecules. [provided by RefSeq, Jul 2008]","start":145719471,"end":145739288,"strand":1,"description":"CD160 molecule [Source:HGNC Symbol;Acc:HGNC:17013]"}, {"versioned_ensembl_gene_id":"ENSG00000168003.16","gene_symbol":"SLC3A2","gene_name":"solute carrier family 3 member 2 [Source:HGNC Symbol;Acc:HGNC:11026]","synonyms":"NACAE,MDU1,CD98HC,CD98,4T2HC,4F2HC,4F2","biotype":"protein_coding","ncbi_id":"6520","summary":"This gene is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized. [provided by RefSeq, Nov 2010]","start":62856102,"end":62888875,"strand":1,"description":"solute carrier family 3 member 2 [Source:HGNC Symbol;Acc:HGNC:11026]"}, {"versioned_ensembl_gene_id":"ENSG00000163626.16","gene_symbol":"COX18","gene_name":"COX18, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:26801]","synonyms":"FLJ38991","biotype":"protein_coding","ncbi_id":"285521","summary":"This gene encodes a cytochrome c oxidase assembly protein. The encoded protein is essential for integral membrane protein insertion into the mitochondrial inner membrane. It is also required for cytochrome c oxidase assembly and activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":73052362,"end":73069755,"strand":-1,"description":"COX18, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:26801]"}, {"versioned_ensembl_gene_id":"ENSG00000224574.1","gene_symbol":"COL18A1-AS2","gene_name":"COL18A1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40155]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874236","summary":null,"start":45407386,"end":45410065,"strand":-1,"description":"COL18A1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40155]"}, {"versioned_ensembl_gene_id":"ENSG00000234204.1","gene_symbol":"PIGPP2","gene_name":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45154]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479056","summary":null,"start":62189131,"end":62189953,"strand":1,"description":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45154]"}, {"versioned_ensembl_gene_id":"ENSG00000232644.1","gene_symbol":"AC005297.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26200042,"end":26200647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101871.14","gene_symbol":"MID1","gene_name":"midline 1 [Source:HGNC Symbol;Acc:HGNC:7095]","synonyms":"FXY,TRIM18,RNF59,OS","biotype":"protein_coding","ncbi_id":"4281","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]","start":10445310,"end":10833654,"strand":-1,"description":"midline 1 [Source:HGNC Symbol;Acc:HGNC:7095]"}, {"versioned_ensembl_gene_id":"ENSG00000284716.1","gene_symbol":"AL034417.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7998187,"end":7999934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284747.1","gene_symbol":"AL034417.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7991134,"end":8005312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273931.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54840878,"end":54856485,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000103832.10","gene_symbol":"GOLGA8UP","gene_name":"golgin A8 family member U, pseudogene [Source:HGNC Symbol;Acc:HGNC:44411]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100507067","summary":null,"start":30791573,"end":30801859,"strand":1,"description":"golgin A8 family member U, pseudogene [Source:HGNC Symbol;Acc:HGNC:44411]"}, {"versioned_ensembl_gene_id":"ENSG00000259336.1","gene_symbol":"AC021231.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35099022,"end":35169698,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259592.1","gene_symbol":"PRELID1P4","gene_name":"PRELI domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390572","summary":null,"start":35121573,"end":35122084,"strand":-1,"description":"PRELI domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43889]"}, {"versioned_ensembl_gene_id":"ENSG00000221930.6","gene_symbol":"FAM45BP","gene_name":"family with sequence similarity 45 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30886]","synonyms":"HT011,FAM45B","biotype":"transcribed_processed_pseudogene","ncbi_id":"55855","summary":null,"start":130494965,"end":130496588,"strand":1,"description":"family with sequence similarity 45 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:30886]"}, {"versioned_ensembl_gene_id":"ENSG00000229470.9","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30531607,"end":30547405,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000226729.3","gene_symbol":"AC004815.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119959424,"end":119959754,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251411.1","gene_symbol":"AC093827.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":86913266,"end":86914817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092621.12","gene_symbol":"PHGDH","gene_name":"phosphoglycerate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8923]","synonyms":"SERA,PGDH,PDG","biotype":"protein_coding","ncbi_id":"26227","summary":"This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly, psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found, however the full-length nature of most are not known. [provided by RefSeq, Aug 2011]","start":119648411,"end":119744226,"strand":1,"description":"phosphoglycerate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8923]"}, {"versioned_ensembl_gene_id":"ENSG00000235043.3","gene_symbol":"TECRP1","gene_name":"trans-2,3-enoyl-CoA reductase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44050]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442777","summary":null,"start":86949669,"end":86950113,"strand":-1,"description":"trans-2,3-enoyl-CoA reductase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44050]"}, {"versioned_ensembl_gene_id":"ENSG00000175336.9","gene_symbol":"APOF","gene_name":"apolipoprotein F [Source:HGNC Symbol;Acc:HGNC:615]","synonyms":null,"biotype":"protein_coding","ncbi_id":"319","summary":"The product of this gene is one of the minor apolipoproteins found in plasma. This protein forms complexes with lipoproteins and may be involved in transport and/or esterification of cholesterol. [provided by RefSeq, Jul 2008]","start":56360569,"end":56362823,"strand":-1,"description":"apolipoprotein F [Source:HGNC Symbol;Acc:HGNC:615]"}, {"versioned_ensembl_gene_id":"ENSG00000265188.1","gene_symbol":"AP001496.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5240255,"end":5241167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271349.1","gene_symbol":"AC007992.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":96126967,"end":96127801,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228852.6","gene_symbol":"AC092802.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":95243167,"end":95278940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243744.2","gene_symbol":"AC016546.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13637919,"end":13638381,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271092.5","gene_symbol":"TMEM56-RWDD3","gene_name":"TMEM56-RWDD3 readthrough [Source:HGNC Symbol;Acc:HGNC:49388]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527978","summary":"This locus represents naturally occurring read-through transcription between the neighboring TMEM56 (transmembrane protein 56) and RWDD3 (RWD domain containing 3) genes on chromosome 1. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product, but it contains a distinct C-terminus due to frameshifts versus the downstream gene coding sequence. [provided by RefSeq, Dec 2010]","start":95117923,"end":95247225,"strand":1,"description":"TMEM56-RWDD3 readthrough [Source:HGNC Symbol;Acc:HGNC:49388]"}, {"versioned_ensembl_gene_id":"ENSG00000117748.9","gene_symbol":"RPA2","gene_name":"replication protein A2 [Source:HGNC Symbol;Acc:HGNC:10290]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6118","summary":"This gene encodes a subunit of the heterotrimeric Replication Protein A (RPA) complex, which binds to single-stranded DNA (ssDNA), forming a nucleoprotein complex that plays an important role in DNA metabolism, being involved in DNA replication, repair, recombination, telomere maintenance, and co-ordinating the cellular response to DNA damage through activation of the ataxia telangiectasia and Rad3-related protein (ATR) kinase. The RPA complex protects single-stranded DNA from nucleases, prevents formation of secondary structures that would interfere with repair, and co-ordinates the recruitment and departure of different genome maintenance factors. The heterotrimeric complex has two different modes of ssDNA binding, a low-affinity and high-affinity mode, determined by which oligonucleotide/oligosaccharide-binding (OB) domains of the complex are utilized, and differing in the length of DNA bound. This subunit contains a single OB domain that participates in high-affinity DNA binding and also contains a winged helix domain at its carboxy terminus, which interacts with many genome maintenance protein. Post-translational modifications of the RPA complex also plays a role in co-ordinating different damage response pathways. [provided by RefSeq, Sep 2017]","start":27891524,"end":27914746,"strand":-1,"description":"replication protein A2 [Source:HGNC Symbol;Acc:HGNC:10290]"}, {"versioned_ensembl_gene_id":"ENSG00000261481.1","gene_symbol":"AC022167.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8869251,"end":8870032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229382.1","gene_symbol":"BX322557.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45336707,"end":45338665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226539.1","gene_symbol":"AC012512.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":223704621,"end":223705338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136295.14","gene_symbol":"TTYH3","gene_name":"tweety family member 3 [Source:HGNC Symbol;Acc:HGNC:22222]","synonyms":"KIAA1691","biotype":"protein_coding","ncbi_id":"80727","summary":"This gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+)-activated large conductance chloride(-) channel. [provided by RefSeq, Jul 2008]","start":2631951,"end":2664802,"strand":1,"description":"tweety family member 3 [Source:HGNC Symbol;Acc:HGNC:22222]"}, {"versioned_ensembl_gene_id":"ENSG00000213849.3","gene_symbol":"AC104306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32507955,"end":32508325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224421.1","gene_symbol":"ATP5J2LP","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2-like pseudogene [Source:HGNC Symbol;Acc:HGNC:849]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101241877","summary":null,"start":36388878,"end":36389112,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2-like pseudogene [Source:HGNC Symbol;Acc:HGNC:849]"}, {"versioned_ensembl_gene_id":"ENSG00000217030.1","gene_symbol":"AL359643.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4979072,"end":4979494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238122.1","gene_symbol":"AL359258.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108261196,"end":108273689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211797.2","gene_symbol":"TRAV17","gene_name":"T-cell receptor alpha variable 17 [Source:HGNC Symbol;Acc:HGNC:12113]","synonyms":"TCRAV17S1,TCRAV3S1","biotype":"TR_V_gene","ncbi_id":"28666","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21997539,"end":21998168,"strand":1,"description":"T-cell receptor alpha variable 17 [Source:HGNC Symbol;Acc:HGNC:12113]"}, {"versioned_ensembl_gene_id":"ENSG00000278083.1","gene_symbol":"AC013476.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":222945930,"end":222946388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241361.8","gene_symbol":"SLC25A24P1","gene_name":"SLC25A24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48933]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727941","summary":null,"start":108272943,"end":108337853,"strand":1,"description":"SLC25A24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48933]"}, {"versioned_ensembl_gene_id":"ENSG00000231902.1","gene_symbol":"AL135923.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7960413,"end":7961080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239994.2","gene_symbol":"AC069444.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119744139,"end":119750350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159256.12","gene_symbol":"MORC3","gene_name":"MORC family CW-type zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:23572]","synonyms":"KIAA0136,ZCWCC3,ZCW5,NXP2","biotype":"protein_coding","ncbi_id":"23515","summary":"This gene encodes a protein that localizes to the nuclear matrix and forms nuclear bodies via an ATP-dependent mechanism. The protein is predicted to have coiled-coil and zinc finger domains and has RNA binding activity. Alternative splicing produces multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2016]","start":36320189,"end":36386148,"strand":1,"description":"MORC family CW-type zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:23572]"}, {"versioned_ensembl_gene_id":"ENSG00000225335.3","gene_symbol":"AC016027.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18076527,"end":18078884,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213178.3","gene_symbol":"AC074033.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":169483671,"end":169484080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138166.5","gene_symbol":"DUSP5","gene_name":"dual specificity phosphatase 5 [Source:HGNC Symbol;Acc:HGNC:3071]","synonyms":"HVH3","biotype":"protein_coding","ncbi_id":"1847","summary":" The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates ERK1, is expressed in a variety of tissues with the highest levels in pancreas and brain, and is localized in the nucleus. [provided by RefSeq, Jul 2008]","start":110497838,"end":110511544,"strand":1,"description":"dual specificity phosphatase 5 [Source:HGNC Symbol;Acc:HGNC:3071]"}, {"versioned_ensembl_gene_id":"ENSG00000241134.3","gene_symbol":"BET1P1","gene_name":"Bet1 golgi vesicular membrane trafficking protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51363]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128542","summary":null,"start":150749736,"end":150750094,"strand":1,"description":"Bet1 golgi vesicular membrane trafficking protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51363]"}, {"versioned_ensembl_gene_id":"ENSG00000197965.11","gene_symbol":"MPZL1","gene_name":"myelin protein zero like 1 [Source:HGNC Symbol;Acc:HGNC:7226]","synonyms":"PZR,FLJ21047","biotype":"protein_coding","ncbi_id":"9019","summary":null,"start":167721192,"end":167791919,"strand":1,"description":"myelin protein zero like 1 [Source:HGNC Symbol;Acc:HGNC:7226]"}, {"versioned_ensembl_gene_id":"ENSG00000213203.2","gene_symbol":"GIMAP1","gene_name":"GTPase, IMAP family member 1 [Source:HGNC Symbol;Acc:HGNC:23237]","synonyms":"IMAP38,IMAP1,IAN2,HIMAP1","biotype":"protein_coding","ncbi_id":"170575","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. This gene is thought to be involved in the differentiation of T helper (Th) cells of the Th1 lineage, and the related mouse gene has been shown to be critical for the development of mature B and T lymphocytes. Read-through transcription exists between this gene and the downstream GIMAP5 (GTPase, IMAP family member 5) gene. [provided by RefSeq, Dec 2010]","start":150716557,"end":150724284,"strand":1,"description":"GTPase, IMAP family member 1 [Source:HGNC Symbol;Acc:HGNC:23237]"}, {"versioned_ensembl_gene_id":"ENSG00000178654.11","gene_symbol":"PPIAP33","gene_name":"peptidylprolyl isomerase A pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49752]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392285","summary":null,"start":7597823,"end":7598377,"strand":1,"description":"peptidylprolyl isomerase A pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:49752]"}, {"versioned_ensembl_gene_id":"ENSG00000275437.1","gene_symbol":"AL121832.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":62402236,"end":62405935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261240.1","gene_symbol":"AC009065.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2112335,"end":2113342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155980.11","gene_symbol":"KIF5A","gene_name":"kinesin family member 5A [Source:HGNC Symbol;Acc:HGNC:6323]","synonyms":"SPG10,NKHC,MY050,D12S1889","biotype":"protein_coding","ncbi_id":"3798","summary":"This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]","start":57549998,"end":57586632,"strand":1,"description":"kinesin family member 5A [Source:HGNC Symbol;Acc:HGNC:6323]"}, {"versioned_ensembl_gene_id":"ENSG00000235997.2","gene_symbol":"LINC01936","gene_name":"long intergenic non-protein coding RNA 1936 [Source:HGNC Symbol;Acc:HGNC:52759]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30346659,"end":30352431,"strand":1,"description":"long intergenic non-protein coding RNA 1936 [Source:HGNC Symbol;Acc:HGNC:52759]"}, {"versioned_ensembl_gene_id":"ENSG00000213169.3","gene_symbol":"AC069218.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174377244,"end":174378005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175895.3","gene_symbol":"PLEKHF2","gene_name":"pleckstrin homology and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20757]","synonyms":"ZFYVE18,PHAFIN2,FLJ13187","biotype":"protein_coding","ncbi_id":"79666","summary":null,"start":95133804,"end":95156684,"strand":1,"description":"pleckstrin homology and FYVE domain containing 2 [Source:HGNC Symbol;Acc:HGNC:20757]"}, {"versioned_ensembl_gene_id":"ENSG00000230345.1","gene_symbol":"AL121580.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47860671,"end":47862062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206066.3","gene_symbol":"IGLL3P","gene_name":"immunoglobulin lambda like polypeptide 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:5872]","synonyms":"IGLL3,16.1","biotype":"unprocessed_pseudogene","ncbi_id":"91353","summary":null,"start":25318256,"end":25320080,"strand":1,"description":"immunoglobulin lambda like polypeptide 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:5872]"}, {"versioned_ensembl_gene_id":"ENSG00000248567.1","gene_symbol":"AC068721.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71821305,"end":71823980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261150.2","gene_symbol":"EPPK1","gene_name":"epiplakin 1 [Source:HGNC Symbol;Acc:HGNC:15577]","synonyms":"EPIPL1","biotype":"protein_coding","ncbi_id":"83481","summary":"The protein encoded by this gene belongs to the plakin family of proteins, which play a role in the organization of cytoskeletal architecture. This family member is composed of several highly homologous plakin repeats. It may function to maintain the integrity of keratin intermediate filament networks in epithelial cells. Studies of the orthologous mouse protein suggest that it accelerates keratinocyte migration during wound healing. [provided by RefSeq, Oct 2013]","start":143857324,"end":143878464,"strand":-1,"description":"epiplakin 1 [Source:HGNC Symbol;Acc:HGNC:15577]"}, {"versioned_ensembl_gene_id":"ENSG00000142686.7","gene_symbol":"C1orf216","gene_name":"chromosome 1 open reading frame 216 [Source:HGNC Symbol;Acc:HGNC:26800]","synonyms":"FLJ38984","biotype":"protein_coding","ncbi_id":"127703","summary":null,"start":35713875,"end":35719472,"strand":-1,"description":"chromosome 1 open reading frame 216 [Source:HGNC Symbol;Acc:HGNC:26800]"}, {"versioned_ensembl_gene_id":"ENSG00000236682.1","gene_symbol":"AC068282.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127389130,"end":127400580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227610.1","gene_symbol":"FRMPD3-AS1","gene_name":"FRMPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41239]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874122","summary":null,"start":107512983,"end":107545821,"strand":-1,"description":"FRMPD3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41239]"}, {"versioned_ensembl_gene_id":"ENSG00000232795.1","gene_symbol":"SCAND3P1","gene_name":"SCAN domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42037]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873886","summary":null,"start":35185294,"end":35186679,"strand":1,"description":"SCAN domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42037]"}, {"versioned_ensembl_gene_id":"ENSG00000206357.11","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"RDBP,D6S45,RD,RDP,NELF-E","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":31942469,"end":31949469,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000254109.5","gene_symbol":"RBPMS-AS1","gene_name":"RBPMS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48721]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128750","summary":null,"start":30382119,"end":30385401,"strand":-1,"description":"RBPMS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48721]"}, {"versioned_ensembl_gene_id":"ENSG00000260240.4","gene_symbol":"APOOP5","gene_name":"apolipoprotein O pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48743]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"644649","summary":null,"start":59709993,"end":59755026,"strand":-1,"description":"apolipoprotein O pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:48743]"}, {"versioned_ensembl_gene_id":"ENSG00000096155.15","gene_symbol":"BAG6","gene_name":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]","synonyms":"D6S52E,BAT3,G3","biotype":"protein_coding","ncbi_id":"7917","summary":"This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31629248,"end":31642931,"strand":-1,"description":"BCL2 associated athanogene 6 [Source:HGNC Symbol;Acc:HGNC:13919]"}, {"versioned_ensembl_gene_id":"ENSG00000171435.13","gene_symbol":"KSR2","gene_name":"kinase suppressor of ras 2 [Source:HGNC Symbol;Acc:HGNC:18610]","synonyms":"FLJ25965","biotype":"protein_coding","ncbi_id":"283455","summary":null,"start":117453012,"end":117968983,"strand":-1,"description":"kinase suppressor of ras 2 [Source:HGNC Symbol;Acc:HGNC:18610]"}, {"versioned_ensembl_gene_id":"ENSG00000254305.1","gene_symbol":"AC011716.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":76603240,"end":76603852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225225.1","gene_symbol":"ARL2BPP10","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39454]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874449","summary":null,"start":18102457,"end":18103649,"strand":-1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39454]"}, {"versioned_ensembl_gene_id":"ENSG00000229252.6","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30479706,"end":30484444,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000135316.17","gene_symbol":"SYNCRIP","gene_name":"synaptotagmin binding cytoplasmic RNA interacting protein [Source:HGNC Symbol;Acc:HGNC:16918]","synonyms":"NSAP1,HNRPQ1,HNRNPQ,hnRNP-Q,GRY-RBP,dJ3J17.2","biotype":"protein_coding","ncbi_id":"10492","summary":"This gene encodes a member of the cellular heterogeneous nuclear ribonucleoprotein (hnRNP) family. hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA) and regulate alternative splicing, polyadenylation, and other aspects of mRNA metabolism and transport. The encoded protein plays a role in multiple aspects of mRNA maturation and is associated with several multiprotein complexes including the apoB RNA editing-complex and survival of motor neurons (SMN) complex. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 20. [provided by RefSeq, Dec 2011]","start":85607785,"end":85643792,"strand":-1,"description":"synaptotagmin binding cytoplasmic RNA interacting protein [Source:HGNC Symbol;Acc:HGNC:16918]"}, {"versioned_ensembl_gene_id":"ENSG00000259482.1","gene_symbol":"RORA-AS2","gene_name":"RORA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51411]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996876","summary":null,"start":60681569,"end":60686888,"strand":1,"description":"RORA antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:51411]"}, {"versioned_ensembl_gene_id":"ENSG00000226005.3","gene_symbol":"AL513303.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3934519,"end":3935813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198556.13","gene_symbol":"ZNF789","gene_name":"zinc finger protein 789 [Source:HGNC Symbol;Acc:HGNC:27801]","synonyms":null,"biotype":"protein_coding","ncbi_id":"285989","summary":null,"start":99472841,"end":99503650,"strand":1,"description":"zinc finger protein 789 [Source:HGNC Symbol;Acc:HGNC:27801]"}, {"versioned_ensembl_gene_id":"ENSG00000237433.1","gene_symbol":"RPSAP11","gene_name":"ribosomal protein SA pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6503]","synonyms":"LAMRP1,LAMRL1,LAMR1P11,LAMR","biotype":"processed_pseudogene","ncbi_id":"645326","summary":null,"start":32190747,"end":32191627,"strand":1,"description":"ribosomal protein SA pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:6503]"}, {"versioned_ensembl_gene_id":"ENSG00000111305.18","gene_symbol":"GSG1","gene_name":"germ cell associated 1 [Source:HGNC Symbol;Acc:HGNC:19716]","synonyms":"MGC3146","biotype":"protein_coding","ncbi_id":"83445","summary":null,"start":13083560,"end":13103683,"strand":-1,"description":"germ cell associated 1 [Source:HGNC Symbol;Acc:HGNC:19716]"}, {"versioned_ensembl_gene_id":"ENSG00000215319.2","gene_symbol":"EIF5P1","gene_name":"eukaryotic translation initiation factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51465]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421390","summary":null,"start":9818239,"end":9819469,"strand":-1,"description":"eukaryotic translation initiation factor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51465]"}, {"versioned_ensembl_gene_id":"ENSG00000240450.1","gene_symbol":"CSPG4P1Y","gene_name":"chondroitin sulfate proteoglycan 4 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:16478]","synonyms":"CSPG4P1,CSPG4LYP1","biotype":"processed_transcript","ncbi_id":"114758","summary":"There are two copies of this pseudogene within the P1 palindrome on chromosome Y. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":25482908,"end":25486705,"strand":1,"description":"chondroitin sulfate proteoglycan 4 pseudogene 1, Y-linked [Source:HGNC Symbol;Acc:HGNC:16478]"}, {"versioned_ensembl_gene_id":"ENSG00000259751.1","gene_symbol":"AC018868.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34849137,"end":34850395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008735.13","gene_symbol":"MAPK8IP2","gene_name":"mitogen-activated protein kinase 8 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:6883]","synonyms":"PRKM8IPL,JIP2,IB2","biotype":"protein_coding","ncbi_id":"23542","summary":"This gene encodes a scaffold protein that is thought to be involved in the regulation of the c-Jun amino-terminal kinase signaling pathway. This protein has been shown to interact with and regulate the activity of MAPK8/JNK1 and MAP2K7/MKK7 kinases. [provided by RefSeq, Jun 2017]","start":50600685,"end":50613981,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:6883]"}, {"versioned_ensembl_gene_id":"ENSG00000218690.2","gene_symbol":"HIST1H2APS4","gene_name":"histone cluster 1 H2A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4732]","synonyms":"pH2A/k,H2AFKP,H2AFK,dJ34B20.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"8333","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This histone pseudogene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Oct 2015]","start":26272021,"end":26272701,"strand":-1,"description":"histone cluster 1 H2A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4732]"}, {"versioned_ensembl_gene_id":"ENSG00000204740.10","gene_symbol":"MALRD1","gene_name":"MAM and LDL receptor class A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24331]","synonyms":"Diet1,C10orf112,bA265G8.2","biotype":"protein_coding","ncbi_id":"340895","summary":"This gene encodes a conserved protein that features multiple MAM (meprin-A5-protein tyrosine phosphatase mu) and LDLR A2 (low density lipoprotein receptor A2) domains. Expression of this gene is enriched in the small intestine and is upregulated during differentiation of a human cell line that exhibits properties of intestinal epithelial cells. The encoded protein has been shown to modulate production of FGF19 in a human intestinal cell line and may regulate bile acid metabolism in the liver. A synergistic interaction between an allele of this gene and the APOE E4 allele is associated with an elevated risk of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2017]","start":19048771,"end":19790401,"strand":1,"description":"MAM and LDL receptor class A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:24331]"}, {"versioned_ensembl_gene_id":"ENSG00000143393.16","gene_symbol":"PI4KB","gene_name":"phosphatidylinositol 4-kinase beta [Source:HGNC Symbol;Acc:HGNC:8984]","synonyms":"PIK4CB,pi4K92,PI4K-BETA","biotype":"protein_coding","ncbi_id":"5298","summary":null,"start":151291797,"end":151327715,"strand":-1,"description":"phosphatidylinositol 4-kinase beta [Source:HGNC Symbol;Acc:HGNC:8984]"}, {"versioned_ensembl_gene_id":"ENSG00000140830.8","gene_symbol":"TXNL4B","gene_name":"thioredoxin like 4B [Source:HGNC Symbol;Acc:HGNC:26041]","synonyms":"FLJ20511,DLP,Dim2","biotype":"protein_coding","ncbi_id":"54957","summary":null,"start":72044289,"end":72094431,"strand":-1,"description":"thioredoxin like 4B [Source:HGNC Symbol;Acc:HGNC:26041]"}, {"versioned_ensembl_gene_id":"ENSG00000226704.6","gene_symbol":"HSPA1L","gene_name":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]","synonyms":"hum70t,HSP70-HOM","biotype":"protein_coding","ncbi_id":"3305","summary":"This gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein. [provided by RefSeq, Jul 2008]","start":31876648,"end":31882094,"strand":-1,"description":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]"}, {"versioned_ensembl_gene_id":"ENSG00000258225.1","gene_symbol":"AC073571.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78052181,"end":78091737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262888.1","gene_symbol":"AC005736.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3931217,"end":3946305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244289.1","gene_symbol":"AC068587.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12628476,"end":12629256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000011021.21","gene_symbol":"CLCN6","gene_name":"chloride voltage-gated channel 6 [Source:HGNC Symbol;Acc:HGNC:2024]","synonyms":"KIAA0046,CLC-6","biotype":"protein_coding","ncbi_id":"1185","summary":"This gene encodes a member of the voltage-dependent chloride channel protein family. Members of this family can function as either chloride channels or antiporters. This protein is primarily localized to late endosomes and functions as a chloride/proton antiporter. Alternate splicing results in both coding and non-coding variants. Additional alternately spliced variants have been described but their full-length structure is unknown. [provided by RefSeq, Mar 2012]","start":11806096,"end":11843144,"strand":1,"description":"chloride voltage-gated channel 6 [Source:HGNC Symbol;Acc:HGNC:2024]"}, {"versioned_ensembl_gene_id":"ENSG00000184277.12","gene_symbol":"TM2D3","gene_name":"TM2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24128]","synonyms":"FLJ22604,BLP2","biotype":"protein_coding","ncbi_id":"80213","summary":"The protein encoded by this gene contains a structural module related to that of the seven transmembrane domain G protein-coupled receptor superfamily. This protein has sequence and structural similarities to the beta-amyloid binding protein (BBP), but, unlike BBP, it does not regulate a response to beta-amyloid peptide. This protein may have regulatory roles in cell death or proliferation signal cascades. Several alternatively spliced transcript variants of this gene are described but the full length nature of some variants has not been determined. Multiple polyadenylation sites have been found in this gene. [provided by RefSeq, Jul 2008]","start":101621444,"end":101652391,"strand":-1,"description":"TM2 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24128]"}, {"versioned_ensembl_gene_id":"ENSG00000213569.4","gene_symbol":"AL390039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107131659,"end":107132269,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226555.1","gene_symbol":"AGKP1","gene_name":"acylglycerol kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37661]","synonyms":"AGKY1","biotype":"processed_pseudogene","ncbi_id":"359793","summary":null,"start":14639096,"end":14640358,"strand":1,"description":"acylglycerol kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37661]"}, {"versioned_ensembl_gene_id":"ENSG00000165566.12","gene_symbol":"AMER2","gene_name":"APC membrane recruitment protein 2 [Source:HGNC Symbol;Acc:HGNC:26360]","synonyms":"FLJ25477,FAM123A","biotype":"protein_coding","ncbi_id":"219287","summary":null,"start":25161684,"end":25172288,"strand":-1,"description":"APC membrane recruitment protein 2 [Source:HGNC Symbol;Acc:HGNC:26360]"}, {"versioned_ensembl_gene_id":"ENSG00000282083.1","gene_symbol":"AC015849.7","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":35818399,"end":35823713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136247.14","gene_symbol":"ZDHHC4","gene_name":"zinc finger DHHC-type containing 4 [Source:HGNC Symbol;Acc:HGNC:18471]","synonyms":"FLJ10479,ZNF374","biotype":"protein_coding","ncbi_id":"55146","summary":null,"start":6577434,"end":6589374,"strand":1,"description":"zinc finger DHHC-type containing 4 [Source:HGNC Symbol;Acc:HGNC:18471]"}, {"versioned_ensembl_gene_id":"ENSG00000125637.15","gene_symbol":"PSD4","gene_name":"pleckstrin and Sec7 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19096]","synonyms":"TIC,EFA6B","biotype":"protein_coding","ncbi_id":"23550","summary":null,"start":113157325,"end":113209396,"strand":1,"description":"pleckstrin and Sec7 domain containing 4 [Source:HGNC Symbol;Acc:HGNC:19096]"}, {"versioned_ensembl_gene_id":"ENSG00000232581.1","gene_symbol":"AC079742.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6578565,"end":6588974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277661.4","gene_symbol":"AL662791.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29036021,"end":29076524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283069.1","gene_symbol":"ABBA01031660.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29318824,"end":29319579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144036.15","gene_symbol":"EXOC6B","gene_name":"exocyst complex component 6B [Source:HGNC Symbol;Acc:HGNC:17085]","synonyms":"SEC15L2,SEC15B,KIAA0919","biotype":"protein_coding","ncbi_id":"23233","summary":"This gene encodes a protein which is a part of the evolutionarily conserved exocyst, a multimeric protein complex necessary for exocytosis, which in turn, is crucial for cell growth, polarity and migration. Disruption of this gene may be associated with phenotypes exhibiting multiple symptoms including intellectual disability and developmental delay (DD). [provided by RefSeq, Jun 2016]","start":72175984,"end":72826041,"strand":-1,"description":"exocyst complex component 6B [Source:HGNC Symbol;Acc:HGNC:17085]"}, {"versioned_ensembl_gene_id":"ENSG00000265128.1","gene_symbol":"AC016866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49116301,"end":49126479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231860.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30766979,"end":30777095,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000227009.1","gene_symbol":"FUNDC2P4","gene_name":"FUN14 domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37971]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127979","summary":null,"start":39155525,"end":39155945,"strand":1,"description":"FUN14 domain containing 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37971]"}, {"versioned_ensembl_gene_id":"ENSG00000111875.7","gene_symbol":"ASF1A","gene_name":"anti-silencing function 1A histone chaperone [Source:HGNC Symbol;Acc:HGNC:20995]","synonyms":"DKFZP547E2110,CIA","biotype":"protein_coding","ncbi_id":"25842","summary":"This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The protein is a key component of a histone donor complex that functions in nucleosome assembly. It interacts with histones H3 and H4, and functions together with a chromatin assembly factor during DNA replication and repair. [provided by RefSeq, Jul 2008]","start":118894220,"end":118909167,"strand":1,"description":"anti-silencing function 1A histone chaperone [Source:HGNC Symbol;Acc:HGNC:20995]"}, {"versioned_ensembl_gene_id":"ENSG00000235299.2","gene_symbol":"MRPL53P1","gene_name":"mitochondrial ribosomal protein L53 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29725]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359752","summary":null,"start":112625906,"end":112626224,"strand":-1,"description":"mitochondrial ribosomal protein L53 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29725]"}, {"versioned_ensembl_gene_id":"ENSG00000189221.9","gene_symbol":"MAOA","gene_name":"monoamine oxidase A [Source:HGNC Symbol;Acc:HGNC:6833]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4128","summary":"This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012]","start":43654907,"end":43746824,"strand":1,"description":"monoamine oxidase A [Source:HGNC Symbol;Acc:HGNC:6833]"}, {"versioned_ensembl_gene_id":"ENSG00000235134.7","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"CPS1,CYP21B,CAH1,CYP21,CA21H,P450c21B","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32114742,"end":32118110,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000094916.15","gene_symbol":"CBX5","gene_name":"chromobox 5 [Source:HGNC Symbol;Acc:HGNC:1555]","synonyms":"HP1-ALPHA,HP1,HP1Hs-alpha","biotype":"protein_coding","ncbi_id":"23468","summary":"This gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N-terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C-terminal chromo shadow-domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin-associated nonhistone proteins. The encoded product is involved in the formation of functional kinetochore through interaction with essential kinetochore proteins. The gene has a pseudogene located on chromosome 3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]","start":54230940,"end":54280133,"strand":-1,"description":"chromobox 5 [Source:HGNC Symbol;Acc:HGNC:1555]"}, {"versioned_ensembl_gene_id":"ENSG00000276035.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786406,"end":54790261,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000254527.1","gene_symbol":"ENPP7P12","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480230","summary":null,"start":12205759,"end":12206389,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:48697]"}, {"versioned_ensembl_gene_id":"ENSG00000236794.5","gene_symbol":"BCRP8","gene_name":"breakpoint cluster region pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39076]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133044","summary":null,"start":23179918,"end":23180172,"strand":-1,"description":"breakpoint cluster region pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39076]"}, {"versioned_ensembl_gene_id":"ENSG00000204177.10","gene_symbol":"BMS1P1","gene_name":"BMS1, ribosome biogenesis factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23649]","synonyms":"BMS1LP5,BMS1LP1,BMS1P5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46786674,"end":46811989,"strand":1,"description":"BMS1, ribosome biogenesis factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23649]"}, {"versioned_ensembl_gene_id":"ENSG00000256350.1","gene_symbol":"AC243972.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21698954,"end":21699151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067064.10","gene_symbol":"IDI1","gene_name":"isopentenyl-diphosphate delta isomerase 1 [Source:HGNC Symbol;Acc:HGNC:5387]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3422","summary":"IDI1 encodes a peroxisomally-localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP), which are the substrates for the successive reaction that results in the synthesis of farnesyl diphosphate and, ultimately, cholesterol. It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity. [provided by RefSeq, Jul 2008]","start":1039908,"end":1049170,"strand":-1,"description":"isopentenyl-diphosphate delta isomerase 1 [Source:HGNC Symbol;Acc:HGNC:5387]"}, {"versioned_ensembl_gene_id":"ENSG00000226024.1","gene_symbol":"COX5BP7","gene_name":"cytochrome c oxidase subunit 5B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:2276]","synonyms":"COX5BL7","biotype":"processed_pseudogene","ncbi_id":"1336","summary":null,"start":39120293,"end":39120566,"strand":-1,"description":"cytochrome c oxidase subunit 5B pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:2276]"}, {"versioned_ensembl_gene_id":"ENSG00000213493.3","gene_symbol":"ACTN4P1","gene_name":"actinin alpha 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44028]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344978","summary":null,"start":116598161,"end":116599611,"strand":1,"description":"actinin alpha 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44028]"}, {"versioned_ensembl_gene_id":"ENSG00000177674.15","gene_symbol":"AGTRAP","gene_name":"angiotensin II receptor associated protein [Source:HGNC Symbol;Acc:HGNC:13539]","synonyms":"ATRAP","biotype":"protein_coding","ncbi_id":"57085","summary":"This gene encodes a transmembrane protein localized to the plasma membrane and perinuclear vesicular structures. The gene product interacts with the angiotensin II type I receptor and negatively regulates angiotensin II signaling. Alternative splicing of this gene generates multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":11736084,"end":11754802,"strand":1,"description":"angiotensin II receptor associated protein [Source:HGNC Symbol;Acc:HGNC:13539]"}, {"versioned_ensembl_gene_id":"ENSG00000119541.9","gene_symbol":"VPS4B","gene_name":"vacuolar protein sorting 4 homolog B [Source:HGNC Symbol;Acc:HGNC:10895]","synonyms":"VPS4-2,SKD1B,SKD1","biotype":"protein_coding","ncbi_id":"9525","summary":"The protein encoded by this gene is a member of the AAA protein family (ATPases associated with diverse cellular activities), and is the homolog of the yeast Vps4 protein. In humans, two paralogs of the yeast protein have been identified. The former share a high degree of aa sequence similarity with each other, and also with yeast Vps4 and mouse Skd1 proteins. Mouse Skd1 (suppressor of K+ transport defect 1) has been shown to be a yeast Vps4 ortholog. Functional studies indicate that both human paralogs associate with the endosomal compartments, and are involved in intracellular protein trafficking, similar to Vps4 protein in yeast. The gene encoding this paralog has been mapped to chromosome 18; the gene for the other resides on chromosome 16. [provided by RefSeq, Jul 2008]","start":63389190,"end":63422483,"strand":-1,"description":"vacuolar protein sorting 4 homolog B [Source:HGNC Symbol;Acc:HGNC:10895]"}, {"versioned_ensembl_gene_id":"ENSG00000138942.15","gene_symbol":"RNF185","gene_name":"ring finger protein 185 [Source:HGNC Symbol;Acc:HGNC:26783]","synonyms":"FLJ38628","biotype":"protein_coding","ncbi_id":"91445","summary":null,"start":31160183,"end":31207019,"strand":1,"description":"ring finger protein 185 [Source:HGNC Symbol;Acc:HGNC:26783]"}, {"versioned_ensembl_gene_id":"ENSG00000254835.1","gene_symbol":"RNF185-AS1","gene_name":"RNF185 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41161]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100852405","summary":null,"start":31205264,"end":31205616,"strand":-1,"description":"RNF185 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41161]"}, {"versioned_ensembl_gene_id":"ENSG00000148377.5","gene_symbol":"IDI2","gene_name":"isopentenyl-diphosphate delta isomerase 2 [Source:HGNC Symbol;Acc:HGNC:23487]","synonyms":"IPPI2","biotype":"protein_coding","ncbi_id":"91734","summary":"The protein encoded by this gene catalyzes the conversion of isopentenyl diphosphate to dimethylallyl diphosphate, which is a precursor for the synthesis of cholesterol and other isoprenoids. This gene, which is a product of an ancestral gene duplication event, encodes a protein that may be involved in the aggregation of alpha-synuclein in the cerebral cortex of patients with Lewy body disease. In addition, segmental copy number gains in this locus have been associated with sporadic amyotrophic lateral sclerosis. [provided by RefSeq, Jul 2016]","start":1018907,"end":1025859,"strand":-1,"description":"isopentenyl-diphosphate delta isomerase 2 [Source:HGNC Symbol;Acc:HGNC:23487]"}, {"versioned_ensembl_gene_id":"ENSG00000121361.3","gene_symbol":"KCNJ8","gene_name":"potassium voltage-gated channel subfamily J member 8 [Source:HGNC Symbol;Acc:HGNC:6269]","synonyms":"Kir6.1","biotype":"protein_coding","ncbi_id":"3764","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. Defects in this gene may be a cause of J-wave syndromes and sudden infant death syndrome (SIDS). [provided by RefSeq, May 2012]","start":21764955,"end":21775581,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 8 [Source:HGNC Symbol;Acc:HGNC:6269]"}, {"versioned_ensembl_gene_id":"ENSG00000257239.1","gene_symbol":"AC090630.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41829898,"end":41932592,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168016.13","gene_symbol":"TRANK1","gene_name":"tetratricopeptide repeat and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:29011]","synonyms":"LBA1,KIAA0342","biotype":"protein_coding","ncbi_id":"9881","summary":null,"start":36826820,"end":36945057,"strand":-1,"description":"tetratricopeptide repeat and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:29011]"}, {"versioned_ensembl_gene_id":"ENSG00000242145.1","gene_symbol":"AC099542.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81208193,"end":81208914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136052.9","gene_symbol":"SLC41A2","gene_name":"solute carrier family 41 member 2 [Source:HGNC Symbol;Acc:HGNC:31045]","synonyms":"DKFZP434K0427","biotype":"protein_coding","ncbi_id":"84102","summary":null,"start":104802553,"end":104958744,"strand":-1,"description":"solute carrier family 41 member 2 [Source:HGNC Symbol;Acc:HGNC:31045]"}, {"versioned_ensembl_gene_id":"ENSG00000122644.12","gene_symbol":"ARL4A","gene_name":"ADP ribosylation factor like GTPase 4A [Source:HGNC Symbol;Acc:HGNC:695]","synonyms":"ARL4","biotype":"protein_coding","ncbi_id":"10124","summary":"ADP-ribosylation factor-like 4A is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4A is similar to ARL4C and ARL4D and each has a nuclear localization signal and an unusually high guaninine nucleotide exchange rate. ARL4A is located in both the nuclear and extranuclear cell compartments. Multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":12686856,"end":12690934,"strand":1,"description":"ADP ribosylation factor like GTPase 4A [Source:HGNC Symbol;Acc:HGNC:695]"}, {"versioned_ensembl_gene_id":"ENSG00000227177.1","gene_symbol":"AIMP1P2","gene_name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43693]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873064","summary":null,"start":172885947,"end":172886258,"strand":-1,"description":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43693]"}, {"versioned_ensembl_gene_id":"ENSG00000271565.1","gene_symbol":"AL109618.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6219199,"end":6219443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000020219.9","gene_symbol":"CCT8L1P","gene_name":"chaperonin containing TCP1 subunit 8 like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:32153]","synonyms":"CCT8L1","biotype":"processed_pseudogene","ncbi_id":"155100","summary":null,"start":152445477,"end":152447150,"strand":1,"description":"chaperonin containing TCP1 subunit 8 like 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:32153]"}, {"versioned_ensembl_gene_id":"ENSG00000249259.3","gene_symbol":"AC027613.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":115922015,"end":116297160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180138.7","gene_symbol":"CSNK1A1L","gene_name":"casein kinase 1 alpha 1 like [Source:HGNC Symbol;Acc:HGNC:20289]","synonyms":"MGC33182","biotype":"protein_coding","ncbi_id":"122011","summary":null,"start":37103259,"end":37105664,"strand":-1,"description":"casein kinase 1 alpha 1 like [Source:HGNC Symbol;Acc:HGNC:20289]"}, {"versioned_ensembl_gene_id":"ENSG00000226871.1","gene_symbol":"AC135178.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8318088,"end":8318712,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277620.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724450,"end":54736092,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000169862.18","gene_symbol":"CTNND2","gene_name":"catenin delta 2 [Source:HGNC Symbol;Acc:HGNC:2516]","synonyms":"GT24,NPRAP","biotype":"protein_coding","ncbi_id":"1501","summary":"This gene encodes an adhesive junction associated protein of the armadillo/beta-catenin superfamily and is implicated in brain and eye development and cancer formation. The protein encoded by this gene promotes the disruption of E-cadherin based adherens junction to favor cell spreading upon stimulation by hepatocyte growth factor. This gene is overexpressed in prostate adenocarcinomas and is associated with decreased expression of tumor suppressor E-cadherin in this tissue. This gene resides in a region of the short arm of chromosome 5 that is deleted in Cri du Chat syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]","start":10971840,"end":11904043,"strand":-1,"description":"catenin delta 2 [Source:HGNC Symbol;Acc:HGNC:2516]"}, {"versioned_ensembl_gene_id":"ENSG00000048544.5","gene_symbol":"MRPS10","gene_name":"mitochondrial ribosomal protein S10 [Source:HGNC Symbol;Acc:HGNC:14502]","synonyms":"FLJ10567","biotype":"protein_coding","ncbi_id":"55173","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S10P family. Pseudogenes corresponding to this gene are found on chromosomes 1q, 3p, and 9p. [provided by RefSeq, Jul 2008]","start":42206801,"end":42217865,"strand":-1,"description":"mitochondrial ribosomal protein S10 [Source:HGNC Symbol;Acc:HGNC:14502]"}, {"versioned_ensembl_gene_id":"ENSG00000171551.11","gene_symbol":"ECEL1","gene_name":"endothelin converting enzyme like 1 [Source:HGNC Symbol;Acc:HGNC:3147]","synonyms":"XCE,DINE","biotype":"protein_coding","ncbi_id":"9427","summary":"This gene encodes a member of the M13 family of endopeptidases. Members of this family are zinc-containing type II integral-membrane proteins that are important regulators of neuropeptide and peptide hormone activity. Mutations in this gene are associated with autosomal recessive distal arthrogryposis, type 5D. This gene has multiple pseudogenes on chromosome 2. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":232479827,"end":232487828,"strand":-1,"description":"endothelin converting enzyme like 1 [Source:HGNC Symbol;Acc:HGNC:3147]"}, {"versioned_ensembl_gene_id":"ENSG00000250467.1","gene_symbol":"AC105389.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41748293,"end":41824119,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282220.1","gene_symbol":"AC110597.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67576038,"end":67583479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179170.11","gene_symbol":"AF186996.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":125747084,"end":125748098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237590.1","gene_symbol":"AL137026.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44259602,"end":44261813,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109132.6","gene_symbol":"PHOX2B","gene_name":"paired like homeobox 2b [Source:HGNC Symbol;Acc:HGNC:9143]","synonyms":"NBPhox,PMX2B,Phox2b","biotype":"protein_coding","ncbi_id":"8929","summary":"The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription factor involved in the development of several major noradrenergic neuron populations and the determination of neurotransmitter phenotype. The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase, c-fos promoters and several enhancers, including cyclic amp-response element and serum-response element. Expansion of a 20 amino acid polyalanine tract in this protein by 5-13 aa has been associated with congenital central hypoventilation syndrome. [provided by RefSeq, Jul 2016]","start":41744082,"end":41748970,"strand":-1,"description":"paired like homeobox 2b [Source:HGNC Symbol;Acc:HGNC:9143]"}, {"versioned_ensembl_gene_id":"ENSG00000277134.5","gene_symbol":"LILRB1","gene_name":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]","synonyms":"CD85,LIR-1,PIR-B,ILT2,MIR-7,CD85j,LIR1,PIRB","biotype":"protein_coding","ncbi_id":"10859","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54638682,"end":54645767,"strand":1,"description":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]"}, {"versioned_ensembl_gene_id":"ENSG00000275274.1","gene_symbol":"LILRB1-AS1","gene_name":"LILRB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53114]","synonyms":"AC009892.10","biotype":"antisense_RNA","ncbi_id":"109729136","summary":null,"start":54643920,"end":54647090,"strand":-1,"description":"LILRB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53114]"}, {"versioned_ensembl_gene_id":"ENSG00000224718.1","gene_symbol":"LINC01657","gene_name":"long intergenic non-protein coding RNA 1657 [Source:HGNC Symbol;Acc:HGNC:52445]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928751","summary":null,"start":175877343,"end":175880468,"strand":1,"description":"long intergenic non-protein coding RNA 1657 [Source:HGNC Symbol;Acc:HGNC:52445]"}, {"versioned_ensembl_gene_id":"ENSG00000273124.1","gene_symbol":"AL365434.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90997480,"end":90997713,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236744.2","gene_symbol":"AC016822.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55247755,"end":55597233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186866.16","gene_symbol":"POFUT2","gene_name":"protein O-fucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14683]","synonyms":"KIAA0958,FUT13,C21orf80","biotype":"protein_coding","ncbi_id":"23275","summary":"Fucose is typically found as a terminal modification of branched chain glycoconjugates, but it also exists in direct O-linkage to serine or threonine residues within cystine knot motifs in epidermal growth factor (EGF; MIM 131530)-like repeats or thrombospondin (THBS; see MIM 188060) type-1 repeats. POFUT2 is an O-fucosyltransferase that use THBS type-1 repeats as substrates (Luo et al., 2006 [PubMed 16464857]).[supplied by OMIM, Mar 2008]","start":45263928,"end":45287898,"strand":-1,"description":"protein O-fucosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:14683]"}, {"versioned_ensembl_gene_id":"ENSG00000274348.2","gene_symbol":"TRPV5","gene_name":"transient receptor potential cation channel subfamily V member 5 [Source:HGNC Symbol;Acc:HGNC:3145]","synonyms":"ECAC1,CaT2","biotype":"protein_coding","ncbi_id":"56302","summary":"This gene is a member of the transient receptor family and the TrpV subfamily. The calcium-selective channel encoded by this gene has 6 transmembrane-spanning domains, multiple potential phosphorylation sites, an N-linked glycosylation site, and 5 ANK repeats. This protein forms homotetramers or heterotetramers and is activated by a low internal calcium level. [provided by RefSeq, Jul 2008]","start":142969288,"end":142994995,"strand":-1,"description":"transient receptor potential cation channel subfamily V member 5 [Source:HGNC Symbol;Acc:HGNC:3145]"}, {"versioned_ensembl_gene_id":"ENSG00000261611.5","gene_symbol":"AC010547.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":71447600,"end":71489311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235222.12","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31727390,"end":31750052,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000215475.4","gene_symbol":"SIAH3","gene_name":"siah E3 ubiquitin protein ligase family member 3 [Source:HGNC Symbol;Acc:HGNC:30553]","synonyms":"FLJ39203","biotype":"protein_coding","ncbi_id":"283514","summary":null,"start":45777243,"end":45851736,"strand":-1,"description":"siah E3 ubiquitin protein ligase family member 3 [Source:HGNC Symbol;Acc:HGNC:30553]"}, {"versioned_ensembl_gene_id":"ENSG00000185436.11","gene_symbol":"IFNLR1","gene_name":"interferon lambda receptor 1 [Source:HGNC Symbol;Acc:HGNC:18584]","synonyms":"IL28RA,IL-28R1,IFNLR,CRF2/12","biotype":"protein_coding","ncbi_id":"163702","summary":"The protein encoded by this gene belongs to the class II cytokine receptor family. This protein forms a receptor complex with interleukine 10 receptor, beta (IL10RB). The receptor complex has been shown to interact with three closely related cytokines, including interleukin 28A (IL28A), interleukin 28B (IL28B), and interleukin 29 (IL29). The expression of all three cytokines can be induced by viral infection. The cells overexpressing this protein have been found to have enhanced responses to IL28A and IL29, but decreased response to IL28B. Three alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":24154157,"end":24187959,"strand":-1,"description":"interferon lambda receptor 1 [Source:HGNC Symbol;Acc:HGNC:18584]"}, {"versioned_ensembl_gene_id":"ENSG00000223494.9","gene_symbol":"VARS2","gene_name":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]","synonyms":"DKFZP434L1435,VARS2L,DKFZP434L1435,KIAA1885,KIAA1885,VARSL,G7a,VARSL,G7a,VARS2L","biotype":"protein_coding","ncbi_id":"57176","summary":"This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":30952885,"end":30971104,"strand":1,"description":"valyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:21642]"}, {"versioned_ensembl_gene_id":"ENSG00000184117.11","gene_symbol":"NIPSNAP1","gene_name":"nipsnap homolog 1 [Source:HGNC Symbol;Acc:HGNC:7827]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8508","summary":"This gene encodes a member of the NipSnap family of proteins that may be involved in vesicular transport. A similar protein in mice inhibits the calcium channel TRPV6, and is also localized to the inner mitochondrial membrane where it may play a role in mitochondrial DNA maintenance. A pseudogene of this gene is located on the short arm of chromosome 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]","start":29554808,"end":29581337,"strand":-1,"description":"nipsnap homolog 1 [Source:HGNC Symbol;Acc:HGNC:7827]"}, {"versioned_ensembl_gene_id":"ENSG00000270505.1","gene_symbol":"IGHV1OR15-1","gene_name":"immunoglobulin heavy variable 1/OR15-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5563]","synonyms":"IGHV1/OR15-1","biotype":"IG_V_gene","ncbi_id":"388077","summary":null,"start":22160431,"end":22160868,"strand":-1,"description":"immunoglobulin heavy variable 1/OR15-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5563]"}, {"versioned_ensembl_gene_id":"ENSG00000154620.5","gene_symbol":"TMSB4Y","gene_name":"thymosin beta 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:11882]","synonyms":"TB4Y","biotype":"protein_coding","ncbi_id":"9087","summary":"This gene lies within the male specific region of chromosome Y. Its homolog on chromosome X escapes X inactivation and encodes an actin sequestering protein. [provided by RefSeq, Jul 2008]","start":13703567,"end":13706024,"strand":1,"description":"thymosin beta 4, Y-linked [Source:HGNC Symbol;Acc:HGNC:11882]"}, {"versioned_ensembl_gene_id":"ENSG00000271029.1","gene_symbol":"AC135178.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8296505,"end":8297216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224902.5","gene_symbol":"GAGE12H","gene_name":"G antigen 12H [Source:HGNC Symbol;Acc:HGNC:31908]","synonyms":"OTTHUMG00000024149","biotype":"protein_coding","ncbi_id":"729442","summary":null,"start":49579983,"end":49587301,"strand":1,"description":"G antigen 12H [Source:HGNC Symbol;Acc:HGNC:31908]"}, {"versioned_ensembl_gene_id":"ENSG00000174015.9","gene_symbol":"SPERT","gene_name":"spermatid associated [Source:HGNC Symbol;Acc:HGNC:30720]","synonyms":"NURIT,CBY2","biotype":"protein_coding","ncbi_id":"220082","summary":null,"start":45702311,"end":45714559,"strand":1,"description":"spermatid associated [Source:HGNC Symbol;Acc:HGNC:30720]"}, {"versioned_ensembl_gene_id":"ENSG00000112237.12","gene_symbol":"CCNC","gene_name":"cyclin C [Source:HGNC Symbol;Acc:HGNC:1581]","synonyms":"CycC","biotype":"protein_coding","ncbi_id":"892","summary":"The protein encoded by this gene is a member of the cyclin family of proteins. The encoded protein interacts with cyclin-dependent kinase 8 and induces the phophorylation of the carboxy-terminal domain of the large subunit of RNA polymerase II. The level of mRNAs for this gene peaks in the G1 phase of the cell cycle. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":99542380,"end":99568973,"strand":-1,"description":"cyclin C [Source:HGNC Symbol;Acc:HGNC:1581]"}, {"versioned_ensembl_gene_id":"ENSG00000254080.1","gene_symbol":"AC115837.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74609698,"end":74633320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008853.16","gene_symbol":"RHOBTB2","gene_name":"Rho related BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18756]","synonyms":"KIAA0717,DBC2","biotype":"protein_coding","ncbi_id":"23221","summary":"The protein encoded by this gene is a small Rho GTPase and a candidate tumor suppressor. The encoded protein interacts with the cullin-3 protein, a ubiquitin E3 ligase necessary for mitotic cell division. This protein inhibits the growth and spread of some types of breast cancer. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":22987417,"end":23020199,"strand":1,"description":"Rho related BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18756]"}, {"versioned_ensembl_gene_id":"ENSG00000259282.5","gene_symbol":"SPATA8-AS1","gene_name":"SPATA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48627]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652749","summary":null,"start":96772005,"end":96783312,"strand":-1,"description":"SPATA8 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48627]"}, {"versioned_ensembl_gene_id":"ENSG00000230287.3","gene_symbol":"AL445928.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":100249090,"end":100249311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251283.1","gene_symbol":"LINC02272","gene_name":"long intergenic non-protein coding RNA 2272 [Source:HGNC Symbol;Acc:HGNC:53187]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986322","summary":null,"start":156634494,"end":156642454,"strand":-1,"description":"long intergenic non-protein coding RNA 2272 [Source:HGNC Symbol;Acc:HGNC:53187]"}, {"versioned_ensembl_gene_id":"ENSG00000144357.16","gene_symbol":"UBR3","gene_name":"ubiquitin protein ligase E3 component n-recognin 3 (putative) [Source:HGNC Symbol;Acc:HGNC:30467]","synonyms":"DKFZp434P117,ZNF650,KIAA2024,FLJ37422","biotype":"protein_coding","ncbi_id":"130507","summary":null,"start":169827458,"end":170084131,"strand":1,"description":"ubiquitin protein ligase E3 component n-recognin 3 (putative) [Source:HGNC Symbol;Acc:HGNC:30467]"}, {"versioned_ensembl_gene_id":"ENSG00000269546.1","gene_symbol":"CLIC4P2","gene_name":"chloride intracellular channel 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49798]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130584","summary":null,"start":6562123,"end":6563848,"strand":-1,"description":"chloride intracellular channel 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49798]"}, {"versioned_ensembl_gene_id":"ENSG00000259534.1","gene_symbol":"AC087477.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96448842,"end":96449749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233946.2","gene_symbol":"RPS29P4","gene_name":"ribosomal protein S29 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35908]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271123","summary":null,"start":175297080,"end":175297240,"strand":1,"description":"ribosomal protein S29 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35908]"}, {"versioned_ensembl_gene_id":"ENSG00000230687.1","gene_symbol":"AL008626.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175203228,"end":175204849,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272163.1","gene_symbol":"AF106564.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24912165,"end":24914717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149016.15","gene_symbol":"TUT1","gene_name":"terminal uridylyl transferase 1, U6 snRNA-specific [Source:HGNC Symbol;Acc:HGNC:26184]","synonyms":"TUTase,RBM21,PAPD2,FLJ22347,FLJ22267,FLJ21850","biotype":"protein_coding","ncbi_id":"64852","summary":"This gene encodes a nucleotidyl transferase that functions as both a terminal uridylyltransferase and a nuclear poly(A) polymerase. The encoded enzyme specifically adds and removes nucleotides from the 3' end of small nuclear RNAs and select mRNAs and may function in controlling gene expression and cell proliferation.[provided by RefSeq, Apr 2009]","start":62575045,"end":62592177,"strand":-1,"description":"terminal uridylyl transferase 1, U6 snRNA-specific [Source:HGNC Symbol;Acc:HGNC:26184]"}, {"versioned_ensembl_gene_id":"ENSG00000250825.1","gene_symbol":"PGAM1P12","gene_name":"phosphoglycerate mutase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42459]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390643","summary":null,"start":96441566,"end":96442313,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42459]"}, {"versioned_ensembl_gene_id":"ENSG00000100422.13","gene_symbol":"CERK","gene_name":"ceramide kinase [Source:HGNC Symbol;Acc:HGNC:19256]","synonyms":"LK4,KIAA1646,hCERK,FLJ23239,FLJ21430,DKFZp434E0211,dA59H18.3,dA59H18.2","biotype":"protein_coding","ncbi_id":"64781","summary":"CERK converts ceramide to ceramide 1-phosphate (C1P), a sphingolipid metabolite. Both CERK and C1P have been implicated in various cellular processes, including proliferation, apoptosis, phagocytosis, and inflammation (Kim et al., 2006 [PubMed 16488390]).[supplied by OMIM, Mar 2008]","start":46684411,"end":46738261,"strand":-1,"description":"ceramide kinase [Source:HGNC Symbol;Acc:HGNC:19256]"}, {"versioned_ensembl_gene_id":"ENSG00000104147.8","gene_symbol":"OIP5","gene_name":"Opa interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:20300]","synonyms":"MIS18B,hMIS18beta,CT86","biotype":"protein_coding","ncbi_id":"11339","summary":"The protein encoded by this gene localizes to centromeres, where it is essential for recruitment of CENP-A through the mediator Holliday junction recognition protein. Expression of this gene is upregulated in several cancers, making it a putative therapeutic target. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":41309268,"end":41332621,"strand":-1,"description":"Opa interacting protein 5 [Source:HGNC Symbol;Acc:HGNC:20300]"}, {"versioned_ensembl_gene_id":"ENSG00000237327.1","gene_symbol":"UPP2-IT1","gene_name":"UPP2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41467]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874283","summary":null,"start":158127957,"end":158133988,"strand":1,"description":"UPP2 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41467]"}, {"versioned_ensembl_gene_id":"ENSG00000104964.14","gene_symbol":"AES","gene_name":"amino-terminal enhancer of split [Source:HGNC Symbol;Acc:HGNC:307]","synonyms":"TLE5,GRG5","biotype":"protein_coding","ncbi_id":"166","summary":"The protein encoded by this gene is similar in sequence to the amino terminus of Drosophila enhancer of split groucho, a protein involved in neurogenesis during embryonic development. The encoded protein, which belongs to the groucho/TLE family of proteins, can function as a homooligomer or as a heteroologimer with other family members to dominantly repress the expression of other family member genes. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":3052910,"end":3063107,"strand":-1,"description":"amino-terminal enhancer of split [Source:HGNC Symbol;Acc:HGNC:307]"}, {"versioned_ensembl_gene_id":"ENSG00000174607.10","gene_symbol":"UGT8","gene_name":"UDP glycosyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:12555]","synonyms":"CGT","biotype":"protein_coding","ncbi_id":"7368","summary":"The protein encoded by this gene belongs to the UDP-glycosyltransferase family. It catalyzes the transfer of galactose to ceramide, a key enzymatic step in the biosynthesis of galactocerebrosides, which are abundant sphingolipids of the myelin membrane of the central and peripheral nervous systems. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2011]","start":114598455,"end":114678224,"strand":1,"description":"UDP glycosyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:12555]"}, {"versioned_ensembl_gene_id":"ENSG00000272540.1","gene_symbol":"AL662797.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30723105,"end":30723877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223877.4","gene_symbol":"RPS8P10","gene_name":"ribosomal protein S8 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35628]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"388076","summary":null,"start":22152276,"end":22152897,"strand":-1,"description":"ribosomal protein S8 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35628]"}, {"versioned_ensembl_gene_id":"ENSG00000125965.8","gene_symbol":"GDF5","gene_name":"growth differentiation factor 5 [Source:HGNC Symbol;Acc:HGNC:4220]","synonyms":"BMP14,CDMP1","biotype":"protein_coding","ncbi_id":"8200","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates the development of numerous tissue and cell types, including cartilage, joints, brown fat, teeth, and the growth of neuronal axons and dendrites. Mutations in this gene are associated with acromesomelic dysplasia, brachydactyly, chondrodysplasia, multiple synostoses syndrome, proximal symphalangism, and susceptibility to osteoarthritis. [provided by RefSeq, Aug 2016]","start":35433347,"end":35454746,"strand":-1,"description":"growth differentiation factor 5 [Source:HGNC Symbol;Acc:HGNC:4220]"}, {"versioned_ensembl_gene_id":"ENSG00000228869.1","gene_symbol":"COX4I1P2","gene_name":"cytochrome c oxidase subunit 4I1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38036]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652170","summary":null,"start":45671845,"end":45672391,"strand":1,"description":"cytochrome c oxidase subunit 4I1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38036]"}, {"versioned_ensembl_gene_id":"ENSG00000228941.1","gene_symbol":"UBE3AP2","gene_name":"ubiquitin protein ligase E3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"7339","summary":null,"start":31060600,"end":31063168,"strand":-1,"description":"ubiquitin protein ligase E3A pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:12498]"}, {"versioned_ensembl_gene_id":"ENSG00000278182.1","gene_symbol":"AC239860.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":145507444,"end":145508607,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197385.5","gene_symbol":"ZNF860","gene_name":"zinc finger protein 860 [Source:HGNC Symbol;Acc:HGNC:34513]","synonyms":null,"biotype":"protein_coding","ncbi_id":"344787","summary":null,"start":31981771,"end":31991628,"strand":1,"description":"zinc finger protein 860 [Source:HGNC Symbol;Acc:HGNC:34513]"}, {"versioned_ensembl_gene_id":"ENSG00000140548.9","gene_symbol":"ZNF710","gene_name":"zinc finger protein 710 [Source:HGNC Symbol;Acc:HGNC:25352]","synonyms":"FLJ37393,FLJ00306,DKFZp547K1113","biotype":"protein_coding","ncbi_id":"374655","summary":null,"start":90001392,"end":90082206,"strand":1,"description":"zinc finger protein 710 [Source:HGNC Symbol;Acc:HGNC:25352]"}, {"versioned_ensembl_gene_id":"ENSG00000272975.1","gene_symbol":"MYHAS","gene_name":"myosin heavy chain gene cluster antisense RNA [Source:HGNC Symbol;Acc:HGNC:50609]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128560","summary":null,"start":10383144,"end":10623886,"strand":1,"description":"myosin heavy chain gene cluster antisense RNA [Source:HGNC Symbol;Acc:HGNC:50609]"}, {"versioned_ensembl_gene_id":"ENSG00000229828.2","gene_symbol":"PDE4DIPP1","gene_name":"phosphodiesterase 4D interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50867]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728920","summary":null,"start":148080598,"end":148093883,"strand":1,"description":"phosphodiesterase 4D interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50867]"}, {"versioned_ensembl_gene_id":"ENSG00000223930.5","gene_symbol":"AC109779.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178202050,"end":178385417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267249.1","gene_symbol":"AP005482.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":12670426,"end":12671145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232797.1","gene_symbol":"FAM207CP","gene_name":"family with sequence similarity 207 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:42676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727987","summary":null,"start":13792635,"end":13793141,"strand":1,"description":"family with sequence similarity 207 member C, pseudogene [Source:HGNC Symbol;Acc:HGNC:42676]"}, {"versioned_ensembl_gene_id":"ENSG00000279092.1","gene_symbol":"AC025678.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34415450,"end":34420273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260639.1","gene_symbol":"AC025678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34394594,"end":34394931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267108.1","gene_symbol":"AP001029.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12432897,"end":12437635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167098.11","gene_symbol":"SUN5","gene_name":"Sad1 and UNC84 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:16252]","synonyms":"TSARG4,SPAG4L,dJ726C3.1","biotype":"protein_coding","ncbi_id":"140732","summary":"The protein encoded by this gene appears to play a role in the meiotic stage of spermatogenesis. The encoded protein localizes to the junction between the sperm head and body and may be involved in nuclear envelope reconstitution and nuclear migration. Mutations in this gene have been implicated in acephalic spermatozoa syndrome. [provided by RefSeq, May 2017]","start":32983773,"end":33004433,"strand":-1,"description":"Sad1 and UNC84 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:16252]"}, {"versioned_ensembl_gene_id":"ENSG00000233047.6","gene_symbol":"LINC01677","gene_name":"long intergenic non-protein coding RNA 1677 [Source:HGNC Symbol;Acc:HGNC:52465]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378884","summary":null,"start":105927624,"end":106028277,"strand":-1,"description":"long intergenic non-protein coding RNA 1677 [Source:HGNC Symbol;Acc:HGNC:52465]"}, {"versioned_ensembl_gene_id":"ENSG00000230932.2","gene_symbol":"AL355306.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":106080801,"end":106081379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125872.7","gene_symbol":"LRRN4","gene_name":"leucine rich repeat neuronal 4 [Source:HGNC Symbol;Acc:HGNC:16208]","synonyms":"NLRR4,dJ1056H1.1,C20orf75","biotype":"protein_coding","ncbi_id":"164312","summary":null,"start":6040778,"end":6054049,"strand":-1,"description":"leucine rich repeat neuronal 4 [Source:HGNC Symbol;Acc:HGNC:16208]"}, {"versioned_ensembl_gene_id":"ENSG00000248576.1","gene_symbol":"AC023794.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54163139,"end":54168595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256884.1","gene_symbol":"AC084880.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119174065,"end":119176484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261068.2","gene_symbol":"AL512274.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42092233,"end":42094259,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236612.1","gene_symbol":"KRTAP19-11P","gene_name":"keratin associated protein 19-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18952]","synonyms":"KRTAP19P3,KAP19C","biotype":"unprocessed_pseudogene","ncbi_id":"337984","summary":null,"start":30537278,"end":30537381,"strand":-1,"description":"keratin associated protein 19-11, pseudogene [Source:HGNC Symbol;Acc:HGNC:18952]"}, {"versioned_ensembl_gene_id":"ENSG00000275525.5","gene_symbol":"LILRA1","gene_name":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]","synonyms":"LIR-6,CD85i,LIR6","biotype":"protein_coding","ncbi_id":"11024","summary":"This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":54601794,"end":54610302,"strand":1,"description":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]"}, {"versioned_ensembl_gene_id":"ENSG00000186977.2","gene_symbol":"KRTAP19-5","gene_name":"keratin associated protein 19-5 [Source:HGNC Symbol;Acc:HGNC:18940]","synonyms":"KAP19.5","biotype":"protein_coding","ncbi_id":"337972","summary":null,"start":30501657,"end":30502117,"strand":-1,"description":"keratin associated protein 19-5 [Source:HGNC Symbol;Acc:HGNC:18940]"}, {"versioned_ensembl_gene_id":"ENSG00000283073.1","gene_symbol":"SMUG1-AS1","gene_name":"SMUG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53307]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369776","summary":null,"start":54142591,"end":54147485,"strand":1,"description":"SMUG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53307]"}, {"versioned_ensembl_gene_id":"ENSG00000250432.5","gene_symbol":"LINC01598","gene_name":"long intergenic non-protein coding RNA 1598 [Source:NCBI gene;Acc:105379478]","synonyms":"TCONS_00028363","biotype":"lincRNA","ncbi_id":"105379478","summary":null,"start":54085132,"end":54125992,"strand":-1,"description":"long intergenic non-protein coding RNA 1598 [Source:NCBI gene;Acc:105379478]"}, {"versioned_ensembl_gene_id":"ENSG00000253993.1","gene_symbol":"AC104027.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33226848,"end":33227147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239775.1","gene_symbol":"AC017116.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":44064908,"end":44066079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263115.1","gene_symbol":"KRTAP9-10P","gene_name":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480422","summary":null,"start":41269234,"end":41269440,"strand":1,"description":"keratin associated protein 9-10, pseudogene [Source:HGNC Symbol;Acc:HGNC:34210]"}, {"versioned_ensembl_gene_id":"ENSG00000157570.11","gene_symbol":"TSPAN18","gene_name":"tetraspanin 18 [Source:HGNC Symbol;Acc:HGNC:20660]","synonyms":"TSPAN","biotype":"protein_coding","ncbi_id":"90139","summary":null,"start":44726465,"end":44932421,"strand":1,"description":"tetraspanin 18 [Source:HGNC Symbol;Acc:HGNC:20660]"}, {"versioned_ensembl_gene_id":"ENSG00000260239.1","gene_symbol":"LINC02533","gene_name":"long intergenic non-protein coding RNA 2533 [Source:HGNC Symbol;Acc:HGNC:53566]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374895","summary":null,"start":4491807,"end":4495769,"strand":1,"description":"long intergenic non-protein coding RNA 2533 [Source:HGNC Symbol;Acc:HGNC:53566]"}, {"versioned_ensembl_gene_id":"ENSG00000167037.18","gene_symbol":"SGSM1","gene_name":"small G protein signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:29410]","synonyms":"RUTBC2,KIAA1941","biotype":"protein_coding","ncbi_id":"129049","summary":null,"start":24806169,"end":24927578,"strand":1,"description":"small G protein signaling modulator 1 [Source:HGNC Symbol;Acc:HGNC:29410]"}, {"versioned_ensembl_gene_id":"ENSG00000275440.1","gene_symbol":"AC009892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54597653,"end":54598499,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284745.1","gene_symbol":"AL589702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2960658,"end":2968707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129187.14","gene_symbol":"DCTD","gene_name":"dCMP deaminase [Source:HGNC Symbol;Acc:HGNC:2710]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1635","summary":"The protein encoded by this gene catalyzes the deamination of dCMP to dUMP, the nucleotide substrate for thymidylate synthase. The encoded protein is allosterically activated by dCTP and inhibited by dTTP, and is found as a homohexamer. This protein uses zinc as a cofactor for its activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":182890060,"end":182917936,"strand":-1,"description":"dCMP deaminase [Source:HGNC Symbol;Acc:HGNC:2710]"}, {"versioned_ensembl_gene_id":"ENSG00000277241.1","gene_symbol":"AC026355.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":177700346,"end":177701072,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276539.4","gene_symbol":"PLPPR1","gene_name":"phospholipid phosphatase related 1 [Source:HGNC Symbol;Acc:HGNC:25993]","synonyms":"LPPR1,FLJ20300,PRG-3,MGC26189","biotype":"protein_coding","ncbi_id":"54886","summary":"This gene encodes a member of the plasticity-related gene (PRG) family. Members of the PRG family mediate lipid phosphate phosphatase activity in neurons and are known to be involved in neuronal plasticity. The protein encoded by this gene does not perform its function through enzymatic phospholipid degradation. This gene is strongly expressed in brain. It shows dynamic expression regulation during brain development and neuronal excitation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]","start":101028709,"end":101325135,"strand":1,"description":"phospholipid phosphatase related 1 [Source:HGNC Symbol;Acc:HGNC:25993]"}, {"versioned_ensembl_gene_id":"ENSG00000115145.9","gene_symbol":"STAM2","gene_name":"signal transducing adaptor molecule 2 [Source:HGNC Symbol;Acc:HGNC:11358]","synonyms":"Hbp","biotype":"protein_coding","ncbi_id":"10254","summary":"The protein encoded by this gene is closely related to STAM, an adaptor protein involved in the downstream signaling of cytokine receptors, both of which contain a SH3 domain and the immunoreceptor tyrosine-based activation motif (ITAM). Similar to STAM, this protein acts downstream of JAK kinases, and is phosphorylated in response to cytokine stimulation. This protein and STAM thus are thought to exhibit compensatory effects on the signaling pathway downstream of JAK kinases upon cytokine stimulation. [provided by RefSeq, Jul 2008]","start":152116801,"end":152175992,"strand":-1,"description":"signal transducing adaptor molecule 2 [Source:HGNC Symbol;Acc:HGNC:11358]"}, {"versioned_ensembl_gene_id":"ENSG00000089818.17","gene_symbol":"NECAP1","gene_name":"NECAP endocytosis associated 1 [Source:HGNC Symbol;Acc:HGNC:24539]","synonyms":"DKFZP566B183","biotype":"protein_coding","ncbi_id":"25977","summary":"This gene encodes a protein containing two characteristic WXXF motifs. The encoded protein localizes to clathrin-coated vesicles, where it binds components of the adapter protein complexes and aids in endocytosis. Loss of function of this gene results in early infantile epileptic encephalopathy-21. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":8076939,"end":8097859,"strand":1,"description":"NECAP endocytosis associated 1 [Source:HGNC Symbol;Acc:HGNC:24539]"}, {"versioned_ensembl_gene_id":"ENSG00000249177.1","gene_symbol":"MTND4P29","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42216]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873250","summary":null,"start":201554384,"end":201556051,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:42216]"}, {"versioned_ensembl_gene_id":"ENSG00000249892.1","gene_symbol":"AC093857.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59767816,"end":59792114,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227439.1","gene_symbol":"TTTY17B","gene_name":"testis-specific transcript, Y-linked 17B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31889]","synonyms":"NCRNA00141","biotype":"lincRNA","ncbi_id":"474151","summary":"There are three copies of this gene on chromosome Y. This record represents the middle copy, which is within the P1 palindrome. [provided by RefSeq, Jul 2008]","start":24485332,"end":24486463,"strand":1,"description":"testis-specific transcript, Y-linked 17B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31889]"}, {"versioned_ensembl_gene_id":"ENSG00000233868.1","gene_symbol":"AC009302.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":221944223,"end":221944612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276550.4","gene_symbol":"HERC2P2","gene_name":"hect domain and RLD 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4870]","synonyms":"D15F37S3","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400322","summary":null,"start":22495570,"end":22590815,"strand":1,"description":"hect domain and RLD 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4870]"}, {"versioned_ensembl_gene_id":"ENSG00000010626.14","gene_symbol":"LRRC23","gene_name":"leucine rich repeat containing 23 [Source:HGNC Symbol;Acc:HGNC:19138]","synonyms":"LRPB7,B7","biotype":"protein_coding","ncbi_id":"10233","summary":null,"start":6873569,"end":6914243,"strand":1,"description":"leucine rich repeat containing 23 [Source:HGNC Symbol;Acc:HGNC:19138]"}, {"versioned_ensembl_gene_id":"ENSG00000278499.2","gene_symbol":"AC018554.3","gene_name":"Putative UPF0607 protein ENSP00000381418 [Source:UniProtKB/Swiss-Prot;Acc:A8MU76]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":60358455,"end":60359480,"strand":-1,"description":"Putative UPF0607 protein ENSP00000381418 [Source:UniProtKB/Swiss-Prot;Acc:A8MU76]"}, {"versioned_ensembl_gene_id":"ENSG00000261026.1","gene_symbol":"AC105046.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":22679013,"end":22684009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251046.2","gene_symbol":"ZNF969P","gene_name":"zinc finger protein 969, pseudogene [Source:HGNC Symbol;Acc:HGNC:44211]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130995","summary":null,"start":110415898,"end":110418504,"strand":1,"description":"zinc finger protein 969, pseudogene [Source:HGNC Symbol;Acc:HGNC:44211]"}, {"versioned_ensembl_gene_id":"ENSG00000170927.14","gene_symbol":"PKHD1","gene_name":"PKHD1, fibrocystin/polyductin [Source:HGNC Symbol;Acc:HGNC:9016]","synonyms":"TIGM1,FPC,FCYT,ARPKD","biotype":"protein_coding","ncbi_id":"5314","summary":"The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008]","start":51615300,"end":52087625,"strand":-1,"description":"PKHD1, fibrocystin/polyductin [Source:HGNC Symbol;Acc:HGNC:9016]"}, {"versioned_ensembl_gene_id":"ENSG00000261485.1","gene_symbol":"PAN3-AS1","gene_name":"PAN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39932]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100288730","summary":null,"start":28136843,"end":28138193,"strand":-1,"description":"PAN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39932]"}, {"versioned_ensembl_gene_id":"ENSG00000224180.8","gene_symbol":"CCHCR1","gene_name":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]","synonyms":"C6orf18,HCR","biotype":"protein_coding","ncbi_id":"54535","summary":"This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]","start":31220974,"end":31236769,"strand":-1,"description":"coiled-coil alpha-helical rod protein 1 [Source:HGNC Symbol;Acc:HGNC:13930]"}, {"versioned_ensembl_gene_id":"ENSG00000282231.1","gene_symbol":"AC233699.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36183607,"end":36196843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250540.1","gene_symbol":"AC104685.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143497412,"end":143498126,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257672.2","gene_symbol":"CR383656.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18614388,"end":18614561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130487.5","gene_symbol":"KLHDC7B","gene_name":"kelch domain containing 7B [Source:HGNC Symbol;Acc:HGNC:25145]","synonyms":"MGC16635","biotype":"protein_coding","ncbi_id":"113730","summary":null,"start":50548033,"end":50551023,"strand":1,"description":"kelch domain containing 7B [Source:HGNC Symbol;Acc:HGNC:25145]"}, {"versioned_ensembl_gene_id":"ENSG00000224494.1","gene_symbol":"HNRNPA3P14","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:48760]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729817","summary":null,"start":81426456,"end":81427605,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:48760]"}, {"versioned_ensembl_gene_id":"ENSG00000277288.3","gene_symbol":"C10orf142","gene_name":"chromosome 10 open reading frame 142 [Source:HGNC Symbol;Acc:HGNC:51236]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130539","summary":null,"start":44292569,"end":44294649,"strand":1,"description":"chromosome 10 open reading frame 142 [Source:HGNC Symbol;Acc:HGNC:51236]"}, {"versioned_ensembl_gene_id":"ENSG00000270165.1","gene_symbol":"AC010530.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":67738588,"end":67739922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242456.1","gene_symbol":"MTCO3P38","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075187","summary":null,"start":166161203,"end":166161968,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52141]"}, {"versioned_ensembl_gene_id":"ENSG00000173153.13","gene_symbol":"ESRRA","gene_name":"estrogen related receptor alpha [Source:HGNC Symbol;Acc:HGNC:3471]","synonyms":"ERR1,NR3B1,ESRL1,ERRalpha,ERRa","biotype":"protein_coding","ncbi_id":"2101","summary":"The protein encoded by this gene is a nuclear receptor that is most closely related to the estrogen receptor. This protein acts as a site-specific transcription factor and interacts with members of the PGC-1 family of transcription cofactors to regulate the expression of most genes involved in cellular energy production as well as in the process of mitochondrial biogenesis. A processed pseudogene of ESRRA is located on chromosome 13q12.1. [provided by RefSeq, Jun 2019]","start":64305572,"end":64316743,"strand":1,"description":"estrogen related receptor alpha [Source:HGNC Symbol;Acc:HGNC:3471]"}, {"versioned_ensembl_gene_id":"ENSG00000274256.1","gene_symbol":"AL391903.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41250851,"end":41251097,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278667.1","gene_symbol":"AC244250.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22730725,"end":22731090,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234399.1","gene_symbol":"RBMY2XP","gene_name":"RNA binding motif protein, Y-linked, family 2, member X pseudogene [Source:HGNC Symbol;Acc:HGNC:23901]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379012","summary":null,"start":24396604,"end":24403526,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member X pseudogene [Source:HGNC Symbol;Acc:HGNC:23901]"}, {"versioned_ensembl_gene_id":"ENSG00000231999.6","gene_symbol":"FLJ27354","gene_name":"uncharacterized LOC400761 [Source:NCBI gene;Acc:400761]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"400761","summary":null,"start":89583241,"end":89632894,"strand":-1,"description":"uncharacterized LOC400761 [Source:NCBI gene;Acc:400761]"}, {"versioned_ensembl_gene_id":"ENSG00000278959.1","gene_symbol":"AC006378.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93954044,"end":93956519,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278157.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54522942,"end":54528379,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000227541.1","gene_symbol":"SFR1P1","gene_name":"SFR1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51531]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130090","summary":null,"start":120202061,"end":120202748,"strand":-1,"description":"SFR1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51531]"}, {"versioned_ensembl_gene_id":"ENSG00000101883.4","gene_symbol":"RHOXF1","gene_name":"Rhox homeobox family member 1 [Source:HGNC Symbol;Acc:HGNC:29993]","synonyms":"OTEX,PEPP1","biotype":"protein_coding","ncbi_id":"158800","summary":"This gene is a member of the PEPP subfamily of paired-like homoebox genes. The gene may be regulated by androgens and epigenetic mechanisms. The encoded nuclear protein is likely a transcription factor that may play a role in human reproduction. [provided by RefSeq, Dec 2012]","start":120109053,"end":120115937,"strand":-1,"description":"Rhox homeobox family member 1 [Source:HGNC Symbol;Acc:HGNC:29993]"}, {"versioned_ensembl_gene_id":"ENSG00000131721.5","gene_symbol":"RHOXF2","gene_name":"Rhox homeobox family member 2 [Source:HGNC Symbol;Acc:HGNC:30011]","synonyms":"THG1,PEPP2,PEPP-2,CT107","biotype":"protein_coding","ncbi_id":"84528","summary":"This gene, which encodes a transcriptional repressor, is one of two paralogous X-linked homeobox-containing genes and is highly expressed in a variety of cancers. In addition, the encoded protein associates with the cell membrane and with microtubules, and is concentrated at the leading edge of migratory cells. [provided by RefSeq, Dec 2015]","start":120158561,"end":120165630,"strand":1,"description":"Rhox homeobox family member 2 [Source:HGNC Symbol;Acc:HGNC:30011]"}, {"versioned_ensembl_gene_id":"ENSG00000228139.1","gene_symbol":"LINC01402","gene_name":"long intergenic non-protein coding RNA 1402 [Source:HGNC Symbol;Acc:HGNC:50685]","synonyms":"TCONS_00017087","biotype":"lincRNA","ncbi_id":"104797536","summary":null,"start":120117642,"end":120119700,"strand":-1,"description":"long intergenic non-protein coding RNA 1402 [Source:HGNC Symbol;Acc:HGNC:50685]"}, {"versioned_ensembl_gene_id":"ENSG00000228917.1","gene_symbol":"AL591806.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":161084465,"end":161087571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124939.5","gene_symbol":"SCGB2A1","gene_name":"secretoglobin family 2A member 1 [Source:HGNC Symbol;Acc:HGNC:7051]","synonyms":"LPHC,UGB3,MGC71973,MGB2","biotype":"protein_coding","ncbi_id":"4246","summary":null,"start":62208668,"end":62213939,"strand":1,"description":"secretoglobin family 2A member 1 [Source:HGNC Symbol;Acc:HGNC:7051]"}, {"versioned_ensembl_gene_id":"ENSG00000124935.3","gene_symbol":"SCGB1D2","gene_name":"secretoglobin family 1D member 2 [Source:HGNC Symbol;Acc:HGNC:18396]","synonyms":"LPHB,LIPB","biotype":"protein_coding","ncbi_id":"10647","summary":"The protein encoded by this gene is a member of the lipophilin subfamily, part of the uteroglobin superfamily, and is an ortholog of prostatein, the major secretory glycoprotein of the rat ventral prostate gland. Lipophilin gene products are widely expressed in normal tissues, especially in endocrine-responsive organs. Assuming that human lipophilins are the functional counterparts of prostatein, they may be transcriptionally regulated by steroid hormones, with the ability to bind androgens, other steroids and possibly bind and concentrate estramustine, a chemotherapeutic agent widely used for prostate cancer. Although the gene has been reported to be on chromosome 10, this sequence appears to be from a cluster of genes on chromosome 11 that includes mammaglobin 2. [provided by RefSeq, Jul 2008]","start":62242210,"end":62244808,"strand":1,"description":"secretoglobin family 1D member 2 [Source:HGNC Symbol;Acc:HGNC:18396]"}, {"versioned_ensembl_gene_id":"ENSG00000175606.10","gene_symbol":"TMEM70","gene_name":"transmembrane protein 70 [Source:HGNC Symbol;Acc:HGNC:26050]","synonyms":"FLJ20533","biotype":"protein_coding","ncbi_id":"54968","summary":"This gene likely encodes a mitochondrial membrane protein. The encoded protein may play a role in biogenesis of mitochondrial ATP synthase. Mutations in this gene have been associated with neonatal mitochondrial encephalocardiomyopathy due to ATP synthase deficiency. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]","start":73972437,"end":73982783,"strand":1,"description":"transmembrane protein 70 [Source:HGNC Symbol;Acc:HGNC:26050]"}, {"versioned_ensembl_gene_id":"ENSG00000251164.1","gene_symbol":"HULC","gene_name":"hepatocellular carcinoma up-regulated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:34232]","synonyms":"NCRNA00078,LINC00078,HCCAT1","biotype":"lincRNA","ncbi_id":"728655","summary":"This gene produces a long RNA that was discovered as upregulated in hepatocellular carcinoma and is associated with cancer progression. Expression of this transcript is regulated by microRNAs and at the transcriptional level by Sp1 family factors. The transcript may regulate gene expression by functioning as a competing RNA for microRNAs. [provided by RefSeq, Dec 2017]","start":8652137,"end":8653846,"strand":1,"description":"hepatocellular carcinoma up-regulated long non-coding RNA [Source:HGNC Symbol;Acc:HGNC:34232]"}, {"versioned_ensembl_gene_id":"ENSG00000182583.12","gene_symbol":"VCX","gene_name":"variable charge, X-linked [Source:HGNC Symbol;Acc:HGNC:12667]","synonyms":"VCX10R,VCX1,VCX-B1,VCX-10r","biotype":"protein_coding","ncbi_id":"26609","summary":"This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. The X-linked members are clustered on chromosome Xp22 and Y-linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. VCX/Y genes encode small and highly charged proteins of unknown function. The presence of a putative bipartite nuclear localization signal suggests that VCX/Y members are nuclear proteins. This gene contains 10 repeats of the 30-bp unit. [provided by RefSeq, Jul 2008]","start":7842262,"end":7844143,"strand":1,"description":"variable charge, X-linked [Source:HGNC Symbol;Acc:HGNC:12667]"}, {"versioned_ensembl_gene_id":"ENSG00000127920.5","gene_symbol":"GNG11","gene_name":"G protein subunit gamma 11 [Source:HGNC Symbol;Acc:HGNC:4403]","synonyms":"GNGT11","biotype":"protein_coding","ncbi_id":"2791","summary":"This gene is a member of the guanine nucleotide-binding protein (G protein) gamma family and encodes a lipid-anchored, cell membrane protein. As a member of the heterotrimeric G protein complex, this protein plays a role in this transmembrane signaling system. This protein is also subject to carboxyl-terminal processing. Decreased expression of this gene is associated with splenic marginal zone lymphomas. [provided by RefSeq, Jul 2008]","start":93921699,"end":93928610,"strand":1,"description":"G protein subunit gamma 11 [Source:HGNC Symbol;Acc:HGNC:4403]"}, {"versioned_ensembl_gene_id":"ENSG00000276278.1","gene_symbol":"AC048382.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84622015,"end":84623237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159239.13","gene_symbol":"AC005041.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":74393836,"end":74421662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226640.2","gene_symbol":"AL357793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":193678894,"end":193727035,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273137.1","gene_symbol":"AL022328.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50208461,"end":50209542,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229619.3","gene_symbol":"MBNL1-AS1","gene_name":"MBNL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44584]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"401093","summary":null,"start":152262616,"end":152269555,"strand":-1,"description":"MBNL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44584]"}, {"versioned_ensembl_gene_id":"ENSG00000196172.9","gene_symbol":"ZNF681","gene_name":"zinc finger protein 681 [Source:HGNC Symbol;Acc:HGNC:26457]","synonyms":"FLJ31526","biotype":"protein_coding","ncbi_id":"148213","summary":null,"start":23739195,"end":23758891,"strand":-1,"description":"zinc finger protein 681 [Source:HGNC Symbol;Acc:HGNC:26457]"}, {"versioned_ensembl_gene_id":"ENSG00000278300.4","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"183ActI,CD158J,cl-49,nkat5","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54476196,"end":54520909,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000215221.2","gene_symbol":"UBA52P6","gene_name":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36763]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130239","summary":null,"start":22012155,"end":22012536,"strand":1,"description":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36763]"}, {"versioned_ensembl_gene_id":"ENSG00000198923.4","gene_symbol":"AC011611.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75964799,"end":75964995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227308.2","gene_symbol":"AC009502.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":219685381,"end":219737937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234190.1","gene_symbol":"AC241644.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147777590,"end":147788953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218416.4","gene_symbol":"PP14571","gene_name":"uncharacterized LOC100130449 [Source:NCBI gene;Acc:100130449]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100130449","summary":null,"start":240449315,"end":240456714,"strand":-1,"description":"uncharacterized LOC100130449 [Source:NCBI gene;Acc:100130449]"}, {"versioned_ensembl_gene_id":"ENSG00000226125.1","gene_symbol":"LINC01907","gene_name":"long intergenic non-protein coding RNA 1907 [Source:HGNC Symbol;Acc:HGNC:52726]","synonyms":null,"biotype":"lincRNA","ncbi_id":"151475","summary":null,"start":230690921,"end":230700529,"strand":-1,"description":"long intergenic non-protein coding RNA 1907 [Source:HGNC Symbol;Acc:HGNC:52726]"}, {"versioned_ensembl_gene_id":"ENSG00000185522.8","gene_symbol":"LMNTD2","gene_name":"lamin tail domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28561]","synonyms":"MGC35138,C11orf35","biotype":"protein_coding","ncbi_id":"256329","summary":null,"start":554855,"end":560779,"strand":-1,"description":"lamin tail domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28561]"}, {"versioned_ensembl_gene_id":"ENSG00000162998.4","gene_symbol":"FRZB","gene_name":"frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:3959]","synonyms":"FRZB1,FRZB-PEN,FRZB-1,FRP-3,FRITZ,FRE,SRFP3,SFRP3,hFIZ,FZRB","biotype":"protein_coding","ncbi_id":"2487","summary":"The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility. [provided by RefSeq, Apr 2010]","start":182833275,"end":182867162,"strand":-1,"description":"frizzled-related protein [Source:HGNC Symbol;Acc:HGNC:3959]"}, {"versioned_ensembl_gene_id":"ENSG00000282233.1","gene_symbol":"AL450306.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77782866,"end":77793176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181355.20","gene_symbol":"OFCC1","gene_name":"orofacial cleft 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:21017]","synonyms":"Opo,MRDS1","biotype":"protein_coding","ncbi_id":"266553","summary":null,"start":9596110,"end":10211608,"strand":-1,"description":"orofacial cleft 1 candidate 1 [Source:HGNC Symbol;Acc:HGNC:21017]"}, {"versioned_ensembl_gene_id":"ENSG00000216368.2","gene_symbol":"AL136226.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10118452,"end":10119253,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271843.1","gene_symbol":"AC012557.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64008082,"end":64008692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217624.2","gene_symbol":"AL627402.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41675760,"end":41676494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214362.2","gene_symbol":"RPS3AP36","gene_name":"ribosomal protein S3a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643981","summary":null,"start":95594598,"end":95595372,"strand":1,"description":"ribosomal protein S3a pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:35596]"}, {"versioned_ensembl_gene_id":"ENSG00000101413.11","gene_symbol":"RPRD1B","gene_name":"regulation of nuclear pre-mRNA domain containing 1B [Source:HGNC Symbol;Acc:HGNC:16209]","synonyms":"NET60,Kub5-Hera,K-H,FLJ44520,DKFZp434P0735,dJ1057B20.2,CREPT,C20orf77","biotype":"protein_coding","ncbi_id":"58490","summary":null,"start":38033546,"end":38127780,"strand":1,"description":"regulation of nuclear pre-mRNA domain containing 1B [Source:HGNC Symbol;Acc:HGNC:16209]"}, {"versioned_ensembl_gene_id":"ENSG00000253338.1","gene_symbol":"IGLV3-29","gene_name":"immunoglobulin lambda variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5911]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28790","summary":null,"start":22661299,"end":22661542,"strand":1,"description":"immunoglobulin lambda variable 3-29 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5911]"}, {"versioned_ensembl_gene_id":"ENSG00000217026.3","gene_symbol":"RPL10P1","gene_name":"ribosomal protein L10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10300]","synonyms":"RPL10P","biotype":"processed_pseudogene","ncbi_id":"100288252","summary":null,"start":27420380,"end":27421023,"strand":-1,"description":"ribosomal protein L10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10300]"}, {"versioned_ensembl_gene_id":"ENSG00000130779.19","gene_symbol":"CLIP1","gene_name":"CAP-Gly domain containing linker protein 1 [Source:HGNC Symbol;Acc:HGNC:10461]","synonyms":"RSN,CYLN1,CLIP170,CLIP-170,CLIP","biotype":"protein_coding","ncbi_id":"6249","summary":"The protein encoded by this gene links endocytic vesicles to microtubules. This gene is highly expressed in Reed-Sternberg cells of Hodgkin disease. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":122271432,"end":122422632,"strand":-1,"description":"CAP-Gly domain containing linker protein 1 [Source:HGNC Symbol;Acc:HGNC:10461]"}, {"versioned_ensembl_gene_id":"ENSG00000066382.16","gene_symbol":"MPPED2","gene_name":"metallophosphoesterase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1180]","synonyms":"Hs.46638,FAM1B,dJ873F21.1,dJ1024C24.1,D11S302E,C11orf8,239FB","biotype":"protein_coding","ncbi_id":"744","summary":"This gene likely encodes a metallophosphoesterase. The encoded protein may play a role a brain development. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]","start":30384493,"end":30586872,"strand":-1,"description":"metallophosphoesterase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:1180]"}, {"versioned_ensembl_gene_id":"ENSG00000171860.4","gene_symbol":"C3AR1","gene_name":"complement C3a receptor 1 [Source:HGNC Symbol;Acc:HGNC:1319]","synonyms":"C3AR,AZ3B","biotype":"protein_coding","ncbi_id":"719","summary":"C3a is an anaphylatoxin released during activation of the complement system. The protein encoded by this gene is an orphan G protein-coupled receptor for C3a. Binding of C3a by the encoded receptor activates chemotaxis, granule enzyme release, superoxide anion production, and bacterial opsonization. [provided by RefSeq, May 2016]","start":8058302,"end":8066471,"strand":-1,"description":"complement C3a receptor 1 [Source:HGNC Symbol;Acc:HGNC:1319]"}, {"versioned_ensembl_gene_id":"ENSG00000254489.1","gene_symbol":"AL136088.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30584130,"end":30630508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266891.1","gene_symbol":"AP000902.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9734882,"end":9735602,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266127.1","gene_symbol":"ZNF415P1","gene_name":"zinc finger protein 415 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49869]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419893","summary":null,"start":9785108,"end":9787805,"strand":1,"description":"zinc finger protein 415 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49869]"}, {"versioned_ensembl_gene_id":"ENSG00000254380.1","gene_symbol":"AC093331.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85523899,"end":85540511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261707.1","gene_symbol":"AC092134.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":77741468,"end":77743000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214042.1","gene_symbol":"IFNA7","gene_name":"interferon alpha 7 [Source:HGNC Symbol;Acc:HGNC:5428]","synonyms":"IFNA-J,IFN-alphaJ","biotype":"protein_coding","ncbi_id":"3444","summary":null,"start":21201469,"end":21202205,"strand":-1,"description":"interferon alpha 7 [Source:HGNC Symbol;Acc:HGNC:5428]"}, {"versioned_ensembl_gene_id":"ENSG00000152954.11","gene_symbol":"NRSN1","gene_name":"neurensin 1 [Source:HGNC Symbol;Acc:HGNC:17881]","synonyms":"p24,VMP","biotype":"protein_coding","ncbi_id":"140767","summary":null,"start":24126122,"end":24154900,"strand":1,"description":"neurensin 1 [Source:HGNC Symbol;Acc:HGNC:17881]"}, {"versioned_ensembl_gene_id":"ENSG00000233614.6","gene_symbol":"DDX11L10","gene_name":"DEAD/H-box helicase 11 like 10 [Source:HGNC Symbol;Acc:HGNC:14125]","synonyms":"DDX11P,DDX11L1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100287029","summary":null,"start":11555,"end":14090,"strand":1,"description":"DEAD/H-box helicase 11 like 10 [Source:HGNC Symbol;Acc:HGNC:14125]"}, {"versioned_ensembl_gene_id":"ENSG00000270757.1","gene_symbol":"HSPE1-MOB4","gene_name":"HSPE1-MOB4 readthrough [Source:HGNC Symbol;Acc:HGNC:49184]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529241","summary":"This locus represents naturally occurring read-through transcription between the neighboring HSPE1 (heat shock 10kDa protein 1 (chaperonin 10)) and MOB4 (MOB family member 4, phocein) genes on chromosome 2. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Oct 2011]","start":197500413,"end":197550726,"strand":1,"description":"HSPE1-MOB4 readthrough [Source:HGNC Symbol;Acc:HGNC:49184]"}, {"versioned_ensembl_gene_id":"ENSG00000270159.1","gene_symbol":"AC018695.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85792415,"end":85792933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166823.5","gene_symbol":"MESP1","gene_name":"mesoderm posterior bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:29658]","synonyms":"MGC10676,bHLHc5","biotype":"protein_coding","ncbi_id":"55897","summary":null,"start":89748661,"end":89751310,"strand":-1,"description":"mesoderm posterior bHLH transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:29658]"}, {"versioned_ensembl_gene_id":"ENSG00000219582.3","gene_symbol":"HNRNPA1P58","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:48788]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289286","summary":null,"start":24001824,"end":24002433,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 58 [Source:HGNC Symbol;Acc:HGNC:48788]"}, {"versioned_ensembl_gene_id":"ENSG00000178999.12","gene_symbol":"AURKB","gene_name":"aurora kinase B [Source:HGNC Symbol;Acc:HGNC:11390]","synonyms":"STK5,STK12,PPP1R48,IPL1,AurB,ARK2,AIM-1,Aik2","biotype":"protein_coding","ncbi_id":"9212","summary":"This gene encodes a member of the aurora kinase subfamily of serine/threonine kinases. The genes encoding the other two members of this subfamily are located on chromosomes 19 and 20. These kinases participate in the regulation of alignment and segregation of chromosomes during mitosis and meiosis through association with microtubules. A pseudogene of this gene is located on chromosome 8. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]","start":8204733,"end":8210600,"strand":-1,"description":"aurora kinase B [Source:HGNC Symbol;Acc:HGNC:11390]"}, {"versioned_ensembl_gene_id":"ENSG00000144711.13","gene_symbol":"IQSEC1","gene_name":"IQ motif and Sec7 domain 1 [Source:HGNC Symbol;Acc:HGNC:29112]","synonyms":"KIAA0763,GEP100,BRAG2,ARF-GEP100","biotype":"protein_coding","ncbi_id":"9922","summary":null,"start":12897220,"end":13073117,"strand":-1,"description":"IQ motif and Sec7 domain 1 [Source:HGNC Symbol;Acc:HGNC:29112]"}, {"versioned_ensembl_gene_id":"ENSG00000188153.12","gene_symbol":"COL4A5","gene_name":"collagen type IV alpha 5 chain [Source:HGNC Symbol;Acc:HGNC:2207]","synonyms":"ATS,ASLN","biotype":"protein_coding","ncbi_id":"1287","summary":"This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]","start":108439844,"end":108697545,"strand":1,"description":"collagen type IV alpha 5 chain [Source:HGNC Symbol;Acc:HGNC:2207]"}, {"versioned_ensembl_gene_id":"ENSG00000231362.1","gene_symbol":"AC069271.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13052967,"end":13053122,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225128.1","gene_symbol":"LINC00972","gene_name":"long intergenic non-protein coding RNA 972 [Source:HGNC Symbol;Acc:HGNC:48826]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105375380","summary":null,"start":85421122,"end":85489293,"strand":1,"description":"long intergenic non-protein coding RNA 972 [Source:HGNC Symbol;Acc:HGNC:48826]"}, {"versioned_ensembl_gene_id":"ENSG00000197892.12","gene_symbol":"KIF13B","gene_name":"kinesin family member 13B [Source:HGNC Symbol;Acc:HGNC:14405]","synonyms":"KIAA0639,GAKIN","biotype":"protein_coding","ncbi_id":"23303","summary":null,"start":29067279,"end":29263124,"strand":-1,"description":"kinesin family member 13B [Source:HGNC Symbol;Acc:HGNC:14405]"}, {"versioned_ensembl_gene_id":"ENSG00000259300.2","gene_symbol":"TUBBP8","gene_name":"tubulin beta class I pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101927519","summary":null,"start":29612570,"end":29614274,"strand":1,"description":"tubulin beta class I pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42179]"}, {"versioned_ensembl_gene_id":"ENSG00000131100.12","gene_symbol":"ATP6V1E1","gene_name":"ATPase H+ transporting V1 subunit E1 [Source:HGNC Symbol;Acc:HGNC:857]","synonyms":"Vma4,P31,ATP6V1E,ATP6E2,ATP6E","biotype":"protein_coding","ncbi_id":"529","summary":"This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A, three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. This gene encodes alternate transcriptional splice variants, encoding different V1 domain E subunit isoforms. Pseudogenes for this gene have been found in the genome. [provided by RefSeq, Jul 2008]","start":17592136,"end":17628818,"strand":-1,"description":"ATPase H+ transporting V1 subunit E1 [Source:HGNC Symbol;Acc:HGNC:857]"}, {"versioned_ensembl_gene_id":"ENSG00000250131.1","gene_symbol":"AC078881.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":177444979,"end":177677126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225770.1","gene_symbol":"RPS29P3","gene_name":"ribosomal protein S29 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31363]","synonyms":"bcm2758","biotype":"processed_pseudogene","ncbi_id":"642892","summary":null,"start":196536532,"end":196536702,"strand":1,"description":"ribosomal protein S29 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31363]"}, {"versioned_ensembl_gene_id":"ENSG00000144130.11","gene_symbol":"NT5DC4","gene_name":"5'-nucleotidase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:27678]","synonyms":null,"biotype":"protein_coding","ncbi_id":"284958","summary":null,"start":112721486,"end":112742879,"strand":1,"description":"5'-nucleotidase domain containing 4 [Source:HGNC Symbol;Acc:HGNC:27678]"}, {"versioned_ensembl_gene_id":"ENSG00000130021.13","gene_symbol":"PUDP","gene_name":"pseudouridine 5'-phosphatase [Source:HGNC Symbol;Acc:HGNC:16818]","synonyms":"HDHD1A,HDHD1,GS1,FAM16AX,DXF68S1E","biotype":"protein_coding","ncbi_id":"8226","summary":"This gene encodes a member of the haloacid dehalogenase-like (HAD) hydrolase superfamily. The encoded protein has no known biological function. This gene has a pseudogene on chromosome 1. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2010]","start":7048920,"end":7148190,"strand":-1,"description":"pseudouridine 5'-phosphatase [Source:HGNC Symbol;Acc:HGNC:16818]"}, {"versioned_ensembl_gene_id":"ENSG00000130066.16","gene_symbol":"SAT1","gene_name":"spermidine/spermine N1-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10540]","synonyms":"SAT,SSAT","biotype":"protein_coding","ncbi_id":"6303","summary":"The protein encoded by this gene belongs to the acetyltransferase family, and is a rate-limiting enzyme in the catabolic pathway of polyamine metabolism. It catalyzes the acetylation of spermidine and spermine, and is involved in the regulation of the intracellular concentration of polyamines and their transport out of cells. Defects in this gene are associated with keratosis follicularis spinulosa decalvans (KFSD). Alternatively spliced transcripts have been found for this gene.[provided by RefSeq, Sep 2009]","start":23783173,"end":23786226,"strand":1,"description":"spermidine/spermine N1-acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:10540]"}, {"versioned_ensembl_gene_id":"ENSG00000232516.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30021246,"end":30022535,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000163703.17","gene_symbol":"CRELD1","gene_name":"cysteine rich with EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:14630]","synonyms":"AVSD2","biotype":"protein_coding","ncbi_id":"78987","summary":"This gene encodes a member of a subfamily of epidermal growth factor-related proteins. The encoded protein is characterized by a cysteine-rich with epidermal growth factor-like domain. This protein may function as a cell adhesion molecule. Mutations in this gene are the cause of atrioventricular septal defect. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]","start":9933822,"end":9945413,"strand":1,"description":"cysteine rich with EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:14630]"}, {"versioned_ensembl_gene_id":"ENSG00000234779.1","gene_symbol":"AL450003.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16726814,"end":16727524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102221.13","gene_symbol":"JADE3","gene_name":"jade family PHD finger 3 [Source:HGNC Symbol;Acc:HGNC:22982]","synonyms":"PHF16,KIAA0215,JADE-3","biotype":"protein_coding","ncbi_id":"9767","summary":"This gene encodes a member of a family of large proteins containing PHD (plant homeo domain)-type zinc fingers. The encoded protein may be associated in a nuclear complex that functions in histone H4 acetylation. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2013]","start":46912276,"end":47061242,"strand":1,"description":"jade family PHD finger 3 [Source:HGNC Symbol;Acc:HGNC:22982]"}, {"versioned_ensembl_gene_id":"ENSG00000178826.10","gene_symbol":"TMEM139","gene_name":"transmembrane protein 139 [Source:HGNC Symbol;Acc:HGNC:22058]","synonyms":"FLJ90586","biotype":"protein_coding","ncbi_id":"135932","summary":null,"start":143279957,"end":143288048,"strand":1,"description":"transmembrane protein 139 [Source:HGNC Symbol;Acc:HGNC:22058]"}, {"versioned_ensembl_gene_id":"ENSG00000280369.1","gene_symbol":"AC012640.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10342813,"end":10343131,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231840.1","gene_symbol":"AC073342.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143255264,"end":143287380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250585.2","gene_symbol":"LINC00604","gene_name":"long intergenic non-protein coding RNA 604 [Source:HGNC Symbol;Acc:HGNC:43924]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106144578","summary":null,"start":40240173,"end":40267657,"strand":1,"description":"long intergenic non-protein coding RNA 604 [Source:HGNC Symbol;Acc:HGNC:43924]"}, {"versioned_ensembl_gene_id":"ENSG00000143434.15","gene_symbol":"SEMA6C","gene_name":"semaphorin 6C [Source:HGNC Symbol;Acc:HGNC:10740]","synonyms":"KIAA1869","biotype":"protein_coding","ncbi_id":"10500","summary":"This gene encodes a member of the semaphorin family. Semaphorins represent important molecular signals controlling multiple aspects of the cellular response that follows CNS injury, and thus may play an important role in neural regeneration. [provided by RefSeq, May 2010]","start":151131685,"end":151146664,"strand":-1,"description":"semaphorin 6C [Source:HGNC Symbol;Acc:HGNC:10740]"}, {"versioned_ensembl_gene_id":"ENSG00000280325.1","gene_symbol":"AC074183.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":84939335,"end":84940256,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230333.6","gene_symbol":"AC004160.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":11180902,"end":11520175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231908.1","gene_symbol":"IDH1-AS1","gene_name":"IDH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40292]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507475","summary":null,"start":208255247,"end":208256181,"strand":1,"description":"IDH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40292]"}, {"versioned_ensembl_gene_id":"ENSG00000138413.13","gene_symbol":"IDH1","gene_name":"isocitrate dehydrogenase (NADP(+)) 1, cytosolic [Source:HGNC Symbol;Acc:HGNC:5382]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3417","summary":"Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer. The protein encoded by this gene is the NADP(+)-dependent isocitrate dehydrogenase found in the cytoplasm and peroxisomes. It contains the PTS-1 peroxisomal targeting signal sequence. The presence of this enzyme in peroxisomes suggests roles in the regeneration of NADPH for intraperoxisomal reductions, such as the conversion of 2, 4-dienoyl-CoAs to 3-enoyl-CoAs, as well as in peroxisomal reactions that consume 2-oxoglutarate, namely the alpha-hydroxylation of phytanic acid. The cytoplasmic enzyme serves a significant role in cytoplasmic NADPH production. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013]","start":208236227,"end":208266074,"strand":-1,"description":"isocitrate dehydrogenase (NADP(+)) 1, cytosolic [Source:HGNC Symbol;Acc:HGNC:5382]"}, {"versioned_ensembl_gene_id":"ENSG00000047617.14","gene_symbol":"ANO2","gene_name":"anoctamin 2 [Source:HGNC Symbol;Acc:HGNC:1183]","synonyms":"TMEM16B,C12orf3","biotype":"protein_coding","ncbi_id":"57101","summary":"ANO2 belongs to a family of calcium-activated chloride channels (CaCCs) (reviewed by Hartzell et al., 2009 [PubMed 19015192]).[supplied by OMIM, Jan 2011]","start":5531869,"end":5946232,"strand":-1,"description":"anoctamin 2 [Source:HGNC Symbol;Acc:HGNC:1183]"}, {"versioned_ensembl_gene_id":"ENSG00000224326.1","gene_symbol":"AL136234.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80534978,"end":80584363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255973.1","gene_symbol":"AC137627.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5583797,"end":5584085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197448.13","gene_symbol":"GSTK1","gene_name":"glutathione S-transferase kappa 1 [Source:HGNC Symbol;Acc:HGNC:16906]","synonyms":"GST13","biotype":"protein_coding","ncbi_id":"373156","summary":"This gene encodes a member of the kappa class of the glutathione transferase superfamily of enzymes that function in cellular detoxification. The encoded protein is localized to the peroxisome and catalyzes the conjugation of glutathione to a wide range of hydrophobic substates facilitating the removal of these compounds from cells. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2009]","start":143244093,"end":143270854,"strand":1,"description":"glutathione S-transferase kappa 1 [Source:HGNC Symbol;Acc:HGNC:16906]"}, {"versioned_ensembl_gene_id":"ENSG00000213512.1","gene_symbol":"GBP7","gene_name":"guanylate binding protein 7 [Source:HGNC Symbol;Acc:HGNC:29606]","synonyms":"GBP4L,FLJ38822","biotype":"protein_coding","ncbi_id":"388646","summary":"Guanylate-binding proteins, such as GBP7, are induced by interferon and hydrolyze GTP to both GDP and GMP (Olszewski et al., 2006 [PubMed 16689661]).[supplied by OMIM, Dec 2008]","start":89131751,"end":89176040,"strand":-1,"description":"guanylate binding protein 7 [Source:HGNC Symbol;Acc:HGNC:29606]"}, {"versioned_ensembl_gene_id":"ENSG00000188015.9","gene_symbol":"S100A3","gene_name":"S100 calcium binding protein A3 [Source:HGNC Symbol;Acc:HGNC:10493]","synonyms":"S100E","biotype":"protein_coding","ncbi_id":"6274","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein has the highest content of cysteines of all S100 proteins, has a high affinity for Zinc, and is highly expressed in human hair cuticle. The precise function of this protein is unknown. [provided by RefSeq, Jul 2008]","start":153547329,"end":153549372,"strand":-1,"description":"S100 calcium binding protein A3 [Source:HGNC Symbol;Acc:HGNC:10493]"}, {"versioned_ensembl_gene_id":"ENSG00000263130.1","gene_symbol":"AL513523.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153764082,"end":153768458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263163.5","gene_symbol":"SLC27A3","gene_name":"solute carrier family 27 member 3 [Source:HGNC Symbol;Acc:HGNC:10997]","synonyms":"FATP3,ACSVL3,MGC4365","biotype":"protein_coding","ncbi_id":"11000","summary":"This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":153791585,"end":153797388,"strand":1,"description":"solute carrier family 27 member 3 [Source:HGNC Symbol;Acc:HGNC:10997]"}, {"versioned_ensembl_gene_id":"ENSG00000232530.1","gene_symbol":"LIF-AS1","gene_name":"LIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53473]","synonyms":"Lnc-LIF-AS","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30239194,"end":30240538,"strand":1,"description":"LIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53473]"}, {"versioned_ensembl_gene_id":"ENSG00000249962.1","gene_symbol":"AL157400.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89644603,"end":89645223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205181.5","gene_symbol":"LINC00654","gene_name":"long intergenic non-protein coding RNA 654 [Source:HGNC Symbol;Acc:HGNC:27154]","synonyms":null,"biotype":"lincRNA","ncbi_id":"149837","summary":null,"start":5496067,"end":5504613,"strand":-1,"description":"long intergenic non-protein coding RNA 654 [Source:HGNC Symbol;Acc:HGNC:27154]"}, {"versioned_ensembl_gene_id":"ENSG00000163960.11","gene_symbol":"UBXN7","gene_name":"UBX domain protein 7 [Source:HGNC Symbol;Acc:HGNC:29119]","synonyms":"UBXD7,KIAA0794","biotype":"protein_coding","ncbi_id":"26043","summary":null,"start":196347662,"end":196432474,"strand":-1,"description":"UBX domain protein 7 [Source:HGNC Symbol;Acc:HGNC:29119]"}, {"versioned_ensembl_gene_id":"ENSG00000225822.4","gene_symbol":"UBXN7-AS1","gene_name":"UBXN7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41227]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874034","summary":null,"start":196431385,"end":196432530,"strand":1,"description":"UBXN7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41227]"}, {"versioned_ensembl_gene_id":"ENSG00000178397.12","gene_symbol":"FAM220A","gene_name":"family with sequence similarity 220 member A [Source:HGNC Symbol;Acc:HGNC:22422]","synonyms":"SIPAR,MGC12966,C7orf70,ACPIN1","biotype":"protein_coding","ncbi_id":"84792","summary":null,"start":6329409,"end":6348981,"strand":-1,"description":"family with sequence similarity 220 member A [Source:HGNC Symbol;Acc:HGNC:22422]"}, {"versioned_ensembl_gene_id":"ENSG00000205744.9","gene_symbol":"DENND1C","gene_name":"DENN domain containing 1C [Source:HGNC Symbol;Acc:HGNC:26225]","synonyms":"FLJ22757,FAM31C","biotype":"protein_coding","ncbi_id":"79958","summary":"The protein encoded by this gene functions as a guanine nucleotide exchange factor for the early endosomal small GTPase RAB35, which regulates endosomal membrane trafficking and is involved in actin polymerization. The encoded protein activates RAB35 by promoting the exchange of RAB35-bound GDP for GTP. This gene may play a role in linking RAB35 activation with the clathrin machinery. [provided by RefSeq, May 2017]","start":6467207,"end":6482557,"strand":-1,"description":"DENN domain containing 1C [Source:HGNC Symbol;Acc:HGNC:26225]"}, {"versioned_ensembl_gene_id":"ENSG00000174276.6","gene_symbol":"ZNHIT2","gene_name":"zinc finger HIT-type containing 2 [Source:HGNC Symbol;Acc:HGNC:1177]","synonyms":"FON,C11orf5","biotype":"protein_coding","ncbi_id":"741","summary":null,"start":65116403,"end":65117708,"strand":-1,"description":"zinc finger HIT-type containing 2 [Source:HGNC Symbol;Acc:HGNC:1177]"}, {"versioned_ensembl_gene_id":"ENSG00000275234.1","gene_symbol":"AC010503.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6469465,"end":6470152,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226995.7","gene_symbol":"LINC00658","gene_name":"long intergenic non-protein coding RNA 658 [Source:HGNC Symbol;Acc:HGNC:44315]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507629","summary":null,"start":5426895,"end":5471094,"strand":-1,"description":"long intergenic non-protein coding RNA 658 [Source:HGNC Symbol;Acc:HGNC:44315]"}, {"versioned_ensembl_gene_id":"ENSG00000269067.1","gene_symbol":"ZNF728","gene_name":"zinc finger protein 728 [Source:HGNC Symbol;Acc:HGNC:32463]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388523","summary":null,"start":22975468,"end":23003176,"strand":-1,"description":"zinc finger protein 728 [Source:HGNC Symbol;Acc:HGNC:32463]"}, {"versioned_ensembl_gene_id":"ENSG00000228029.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29945986,"end":29947960,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000276595.4","gene_symbol":"PTCHD3","gene_name":"patched domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24776]","synonyms":"FLJ44037,PTR","biotype":"protein_coding","ncbi_id":"374308","summary":null,"start":27445487,"end":27461668,"strand":-1,"description":"patched domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24776]"}, {"versioned_ensembl_gene_id":"ENSG00000233869.1","gene_symbol":"RPSAP27","gene_name":"ribosomal protein SA pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36650]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130429","summary":null,"start":208208135,"end":208208984,"strand":1,"description":"ribosomal protein SA pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:36650]"}, {"versioned_ensembl_gene_id":"ENSG00000249008.1","gene_symbol":"AC097518.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":177242539,"end":177248773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262513.1","gene_symbol":"AC091996.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":162424378,"end":162427345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281839.1","gene_symbol":"AP001803.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56859642,"end":56882325,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129317.14","gene_symbol":"PUS7L","gene_name":"pseudouridylate synthase 7 like [Source:HGNC Symbol;Acc:HGNC:25276]","synonyms":"DKFZP434G1415","biotype":"protein_coding","ncbi_id":"83448","summary":null,"start":43718993,"end":43758817,"strand":-1,"description":"pseudouridylate synthase 7 like [Source:HGNC Symbol;Acc:HGNC:25276]"}, {"versioned_ensembl_gene_id":"ENSG00000278723.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54655800,"end":54667814,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000229531.5","gene_symbol":"Z99127.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174934947,"end":174954261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223828.1","gene_symbol":"BANF1P4","gene_name":"barrier to autointegration factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43884]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100653423","summary":null,"start":174756850,"end":174757119,"strand":-1,"description":"barrier to autointegration factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43884]"}, {"versioned_ensembl_gene_id":"ENSG00000233247.3","gene_symbol":"AC002524.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14244382,"end":14244928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177989.13","gene_symbol":"ODF3B","gene_name":"outer dense fiber of sperm tails 3B [Source:HGNC Symbol;Acc:HGNC:34388]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440836","summary":null,"start":50529710,"end":50532580,"strand":-1,"description":"outer dense fiber of sperm tails 3B [Source:HGNC Symbol;Acc:HGNC:34388]"}, {"versioned_ensembl_gene_id":"ENSG00000157500.10","gene_symbol":"APPL1","gene_name":"adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 [Source:HGNC Symbol;Acc:HGNC:24035]","synonyms":"APPL","biotype":"protein_coding","ncbi_id":"26060","summary":"The protein encoded by this gene has been shown to be involved in the regulation of cell proliferation, and in the crosstalk between the adiponectin signalling and insulin signalling pathways. The encoded protein binds many other proteins, including RAB5A, DCC, AKT2, PIK3CA, adiponectin receptors, and proteins of the NuRD/MeCP1 complex. This protein is found associated with endosomal membranes, but can be released by EGF and translocated to the nucleus. [provided by RefSeq, Jul 2008]","start":57227737,"end":57273468,"strand":1,"description":"adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 [Source:HGNC Symbol;Acc:HGNC:24035]"}, {"versioned_ensembl_gene_id":"ENSG00000167034.9","gene_symbol":"NKX3-1","gene_name":"NK3 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7838]","synonyms":"NKX3A,NKX3.1,BAPX2","biotype":"protein_coding","ncbi_id":"4824","summary":"This gene encodes a homeobox-containing transcription factor. This transcription factor functions as a negative regulator of epithelial cell growth in prostate tissue. Aberrant expression of this gene is associated with prostate tumor progression. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jan 2012]","start":23678693,"end":23682927,"strand":-1,"description":"NK3 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:7838]"}, {"versioned_ensembl_gene_id":"ENSG00000235946.1","gene_symbol":"AC234783.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104062542,"end":104063037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111665.11","gene_symbol":"CDCA3","gene_name":"cell division cycle associated 3 [Source:HGNC Symbol;Acc:HGNC:14624]","synonyms":"TOME-1,GRCC8","biotype":"protein_coding","ncbi_id":"83461","summary":null,"start":6844793,"end":6852066,"strand":-1,"description":"cell division cycle associated 3 [Source:HGNC Symbol;Acc:HGNC:14624]"}, {"versioned_ensembl_gene_id":"ENSG00000075131.9","gene_symbol":"TIPIN","gene_name":"TIMELESS interacting protein [Source:HGNC Symbol;Acc:HGNC:30750]","synonyms":"FLJ20516","biotype":"protein_coding","ncbi_id":"54962","summary":"The protein encoded by this gene is part of the replisome complex, a group of proteins that support DNA replication. It binds TIM, which is involved in circadian rhythm regulation, and aids in protecting cells against DNA damage and stress. Two pseudogenes and two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":66336206,"end":66386746,"strand":-1,"description":"TIMELESS interacting protein [Source:HGNC Symbol;Acc:HGNC:30750]"}, {"versioned_ensembl_gene_id":"ENSG00000240821.1","gene_symbol":"AC055855.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":66379337,"end":66379915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136235.15","gene_symbol":"GPNMB","gene_name":"glycoprotein nmb [Source:HGNC Symbol;Acc:HGNC:4462]","synonyms":"NMB,HGFIN","biotype":"protein_coding","ncbi_id":"10457","summary":"The protein encoded by this gene is a type I transmembrane glycoprotein which shows homology to the pMEL17 precursor, a melanocyte-specific protein. GPNMB shows expression in the lowly metastatic human melanoma cell lines and xenografts but does not show expression in the highly metastatic cell lines. GPNMB may be involved in growth delay and reduction of metastatic potential. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":23235967,"end":23275108,"strand":1,"description":"glycoprotein nmb [Source:HGNC Symbol;Acc:HGNC:4462]"}, {"versioned_ensembl_gene_id":"ENSG00000100994.11","gene_symbol":"PYGB","gene_name":"glycogen phosphorylase B [Source:HGNC Symbol;Acc:HGNC:9723]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5834","summary":"The protein encoded by this gene is a glycogen phosphorylase found predominantly in the brain. The encoded protein forms homodimers which can associate into homotetramers, the enzymatically active form of glycogen phosphorylase. The activity of this enzyme is positively regulated by AMP and negatively regulated by ATP, ADP, and glucose-6-phosphate. This enzyme catalyzes the rate-determining step in glycogen degradation. [provided by RefSeq, Jul 2008]","start":25248069,"end":25298014,"strand":1,"description":"glycogen phosphorylase B [Source:HGNC Symbol;Acc:HGNC:9723]"}, {"versioned_ensembl_gene_id":"ENSG00000250271.2","gene_symbol":"AC068647.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":151797047,"end":151808249,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172661.17","gene_symbol":"WASHC2C","gene_name":"WASH complex subunit 2C [Source:HGNC Symbol;Acc:HGNC:23414]","synonyms":"KIAA0592,FAM21C,Em:AC012044.3","biotype":"protein_coding","ncbi_id":"253725","summary":null,"start":45727200,"end":45792961,"strand":1,"description":"WASH complex subunit 2C [Source:HGNC Symbol;Acc:HGNC:23414]"}, {"versioned_ensembl_gene_id":"ENSG00000186298.11","gene_symbol":"PPP1CC","gene_name":"protein phosphatase 1 catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9283]","synonyms":"PP1gamma,PP1C","biotype":"protein_coding","ncbi_id":"5501","summary":"The protein encoded by this gene belongs to the protein phosphatase family, PP1 subfamily. PP1 is an ubiquitous serine/threonine phosphatase that regulates many cellular processes, including cell division. It is expressed in mammalian cells as three closely related isoforms, alpha, beta/delta and gamma, which have distinct localization patterns. This gene encodes the gamma isozyme. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":110719680,"end":110742939,"strand":-1,"description":"protein phosphatase 1 catalytic subunit gamma [Source:HGNC Symbol;Acc:HGNC:9283]"}, {"versioned_ensembl_gene_id":"ENSG00000229630.1","gene_symbol":"LINC01264","gene_name":"long intergenic non-protein coding RNA 1264 [Source:HGNC Symbol;Acc:HGNC:50282]","synonyms":"RP11-124O11.2","biotype":"lincRNA","ncbi_id":"104266963","summary":null,"start":42979017,"end":42981507,"strand":-1,"description":"long intergenic non-protein coding RNA 1264 [Source:HGNC Symbol;Acc:HGNC:50282]"}, {"versioned_ensembl_gene_id":"ENSG00000261391.1","gene_symbol":"AC138907.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32715931,"end":32716056,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240201.1","gene_symbol":"AL133372.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30055210,"end":30055954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075234.16","gene_symbol":"TTC38","gene_name":"tetratricopeptide repeat domain 38 [Source:HGNC Symbol;Acc:HGNC:26082]","synonyms":"FLJ20699","biotype":"protein_coding","ncbi_id":"55020","summary":null,"start":46267961,"end":46294008,"strand":1,"description":"tetratricopeptide repeat domain 38 [Source:HGNC Symbol;Acc:HGNC:26082]"}, {"versioned_ensembl_gene_id":"ENSG00000227260.1","gene_symbol":"LINC01985","gene_name":"long intergenic non-protein coding RNA 1985 [Source:HGNC Symbol;Acc:HGNC:52816]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928015","summary":null,"start":30524745,"end":30527185,"strand":1,"description":"long intergenic non-protein coding RNA 1985 [Source:HGNC Symbol;Acc:HGNC:52816]"}, {"versioned_ensembl_gene_id":"ENSG00000176933.5","gene_symbol":"TOB2P1","gene_name":"transducer of ERBB2, 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13986]","synonyms":"TOB4p,TOB2P,p373c6.3","biotype":"processed_pseudogene","ncbi_id":"222699","summary":null,"start":28217643,"end":28218634,"strand":-1,"description":"transducer of ERBB2, 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13986]"}, {"versioned_ensembl_gene_id":"ENSG00000218016.2","gene_symbol":"ZNF192P2","gene_name":"zinc finger protein 192 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42862]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"222701","summary":null,"start":28188050,"end":28189432,"strand":1,"description":"zinc finger protein 192 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42862]"}, {"versioned_ensembl_gene_id":"ENSG00000279223.1","gene_symbol":"AC073342.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":143224042,"end":143224234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255104.8","gene_symbol":"AC005324.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":15699692,"end":15744778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233966.1","gene_symbol":"UBE2SP1","gene_name":"ubiquitin conjugating enzyme E2 S pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246719","summary":null,"start":15704232,"end":15704900,"strand":-1,"description":"ubiquitin conjugating enzyme E2 S pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30864]"}, {"versioned_ensembl_gene_id":"ENSG00000267227.1","gene_symbol":"AC005324.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15748703,"end":15749315,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255198.4","gene_symbol":"SNHG9","gene_name":"small nucleolar RNA host gene 9 [Source:HGNC Symbol;Acc:HGNC:33102]","synonyms":"DKFZp686N06141,NCRNA00062","biotype":"lincRNA","ncbi_id":"735301","summary":null,"start":1964959,"end":1965509,"strand":1,"description":"small nucleolar RNA host gene 9 [Source:HGNC Symbol;Acc:HGNC:33102]"}, {"versioned_ensembl_gene_id":"ENSG00000221937.4","gene_symbol":"TAS2R40","gene_name":"taste 2 receptor member 40 [Source:HGNC Symbol;Acc:HGNC:18885]","synonyms":"GPR60","biotype":"protein_coding","ncbi_id":"259286","summary":"This gene encodes a member of the bitter taste receptor family which belong to the G protein-coupled receptor superfamily and are predominantly expressed in taste receptor cells of the tongue and palate epithelia. This intronless taste receptor gene encodes a seven-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is clustered together with eight other taste receptor genes on chromosome 7. A decrease in the expression of this gene is associated with hypogeusia. [provided by RefSeq, Jul 2017]","start":143222037,"end":143223079,"strand":1,"description":"taste 2 receptor member 40 [Source:HGNC Symbol;Acc:HGNC:18885]"}, {"versioned_ensembl_gene_id":"ENSG00000109536.11","gene_symbol":"FRG1","gene_name":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]","synonyms":"FSG1,FRG1A","biotype":"protein_coding","ncbi_id":"2483","summary":"This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]","start":189940788,"end":189963204,"strand":1,"description":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]"}, {"versioned_ensembl_gene_id":"ENSG00000275543.4","gene_symbol":"MPV17L","gene_name":"MPV17 mitochondrial inner membrane protein like [Source:HGNC Symbol;Acc:HGNC:26827]","synonyms":"MLPH2,MLPH1,FLJ39599,MPV17L1","biotype":"protein_coding","ncbi_id":"255027","summary":null,"start":15480860,"end":15498390,"strand":1,"description":"MPV17 mitochondrial inner membrane protein like [Source:HGNC Symbol;Acc:HGNC:26827]"}, {"versioned_ensembl_gene_id":"ENSG00000282314.1","gene_symbol":"AC243742.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15693630,"end":15695719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276452.4","gene_symbol":"LILRB1","gene_name":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]","synonyms":"CD85,LIR-1,PIR-B,ILT2,MIR-7,CD85j,LIR1,PIRB","biotype":"protein_coding","ncbi_id":"10859","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54388712,"end":54389685,"strand":1,"description":"leukocyte immunoglobulin like receptor B1 [Source:HGNC Symbol;Acc:HGNC:6605]"}, {"versioned_ensembl_gene_id":"ENSG00000279527.1","gene_symbol":"AC073592.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124529722,"end":124530228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107175.11","gene_symbol":"CREB3","gene_name":"cAMP responsive element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:2347]","synonyms":"sLZIP,LZIP,Luman","biotype":"protein_coding","ncbi_id":"10488","summary":"This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds to the cAMP-response element and regulates cell proliferation. The protein interacts with host cell factor C1, which also associates with the herpes simplex virus (HSV) protein VP16 that induces transcription of HSV immediate-early genes. This protein and VP16 both bind to the same site on host cell factor C1. It is thought that the interaction between this protein and host cell factor C1 plays a role in the establishment of latency during HSV infection. This protein also plays a role in leukocyte migration, tumor suppression, and endoplasmic reticulum stress-associated protein degradation. Additional transcript variants have been identified, but their biological validity has not been determined.[provided by RefSeq, Nov 2009]","start":35732335,"end":35737004,"strand":1,"description":"cAMP responsive element binding protein 3 [Source:HGNC Symbol;Acc:HGNC:2347]"}, {"versioned_ensembl_gene_id":"ENSG00000173011.11","gene_symbol":"TADA2B","gene_name":"transcriptional adaptor 2B [Source:HGNC Symbol;Acc:HGNC:30781]","synonyms":"MGC21874","biotype":"protein_coding","ncbi_id":"93624","summary":"TADA2B functions as a transcriptional adaptor protein that potentiates transcription through coordination of histone acetyltransferase (HAT) activity and by linking activation factors to basal transcriptional machinery (Barlev et al., 2003 [PubMed 12972612]).[supplied by OMIM, Apr 2010]","start":7041899,"end":7057952,"strand":1,"description":"transcriptional adaptor 2B [Source:HGNC Symbol;Acc:HGNC:30781]"}, {"versioned_ensembl_gene_id":"ENSG00000241962.9","gene_symbol":"AC079447.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99141485,"end":99322741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158941.16","gene_symbol":"CCAR2","gene_name":"cell cycle and apoptosis regulator 2 [Source:HGNC Symbol;Acc:HGNC:23360]","synonyms":"NET35,KIAA1967,DBC1,DBC-1","biotype":"protein_coding","ncbi_id":"57805","summary":null,"start":22604632,"end":22621514,"strand":1,"description":"cell cycle and apoptosis regulator 2 [Source:HGNC Symbol;Acc:HGNC:23360]"}, {"versioned_ensembl_gene_id":"ENSG00000238279.1","gene_symbol":"BX470102.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153533603,"end":153535115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255117.5","gene_symbol":"LINC02546","gene_name":"long intergenic non-protein coding RNA 2546 [Source:HGNC Symbol;Acc:HGNC:53581]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376606","summary":null,"start":29594918,"end":29630664,"strand":1,"description":"long intergenic non-protein coding RNA 2546 [Source:HGNC Symbol;Acc:HGNC:53581]"}, {"versioned_ensembl_gene_id":"ENSG00000258102.3","gene_symbol":"MAP1LC3B2","gene_name":"microtubule associated protein 1 light chain 3 beta 2 [Source:HGNC Symbol;Acc:HGNC:34390]","synonyms":"ATG8G","biotype":"protein_coding","ncbi_id":"643246","summary":null,"start":116548105,"end":116576448,"strand":1,"description":"microtubule associated protein 1 light chain 3 beta 2 [Source:HGNC Symbol;Acc:HGNC:34390]"}, {"versioned_ensembl_gene_id":"ENSG00000278749.1","gene_symbol":"CCDC166","gene_name":"coiled-coil domain containing 166 [Source:HGNC Symbol;Acc:HGNC:41910]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130274","summary":null,"start":143693701,"end":143695116,"strand":-1,"description":"coiled-coil domain containing 166 [Source:HGNC Symbol;Acc:HGNC:41910]"}, {"versioned_ensembl_gene_id":"ENSG00000248980.1","gene_symbol":"AC019163.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":176308268,"end":176320458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159212.12","gene_symbol":"CLIC6","gene_name":"chloride intracellular channel 6 [Source:HGNC Symbol;Acc:HGNC:2065]","synonyms":"CLIC5,CLIC1L","biotype":"protein_coding","ncbi_id":"54102","summary":"This gene encodes a member of the chloride intracellular channel family of proteins. The gene is part of a large triplicated region found on chromosomes 1, 6, and 21. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2015]","start":34669389,"end":34718227,"strand":1,"description":"chloride intracellular channel 6 [Source:HGNC Symbol;Acc:HGNC:2065]"}, {"versioned_ensembl_gene_id":"ENSG00000131374.14","gene_symbol":"TBC1D5","gene_name":"TBC1 domain family member 5 [Source:HGNC Symbol;Acc:HGNC:19166]","synonyms":"KIAA0210","biotype":"protein_coding","ncbi_id":"9779","summary":null,"start":17157162,"end":18444817,"strand":-1,"description":"TBC1 domain family member 5 [Source:HGNC Symbol;Acc:HGNC:19166]"}, {"versioned_ensembl_gene_id":"ENSG00000224784.2","gene_symbol":"AL591704.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":153396591,"end":153396771,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272882.1","gene_symbol":"OR2BH1P","gene_name":"olfactory receptor family 2 subfamily BH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31250]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403238","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":28986635,"end":28987498,"strand":1,"description":"olfactory receptor family 2 subfamily BH member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31250]"}, {"versioned_ensembl_gene_id":"ENSG00000250739.1","gene_symbol":"LINC01262","gene_name":"long intergenic non-protein coding RNA 1262 [Source:HGNC Symbol;Acc:HGNC:50275]","synonyms":"RP11-462G22.1,TCONS_l2_00021807,TCONS_l2_00021807","biotype":"lincRNA","ncbi_id":"101928971","summary":null,"start":189659605,"end":189661486,"strand":1,"description":"long intergenic non-protein coding RNA 1262 [Source:HGNC Symbol;Acc:HGNC:50275]"}, {"versioned_ensembl_gene_id":"ENSG00000227309.1","gene_symbol":"AC140076.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17465150,"end":17465510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130733.10","gene_symbol":"YIPF2","gene_name":"Yip1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:28476]","synonyms":"MGC3262,FinGER2","biotype":"protein_coding","ncbi_id":"78992","summary":null,"start":10922185,"end":10928681,"strand":-1,"description":"Yip1 domain family member 2 [Source:HGNC Symbol;Acc:HGNC:28476]"}, {"versioned_ensembl_gene_id":"ENSG00000272477.1","gene_symbol":"AC144521.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":18408680,"end":18409635,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273306.1","gene_symbol":"AC018690.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99405218,"end":99405843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272566.1","gene_symbol":"AF250324.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189703881,"end":189704490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008256.15","gene_symbol":"CYTH3","gene_name":"cytohesin 3 [Source:HGNC Symbol;Acc:HGNC:9504]","synonyms":"PSCD3,GRP1,cytohesin-3,ARNO3","biotype":"protein_coding","ncbi_id":"9265","summary":"This gene encodes a member of the PSCD (pleckstrin homology, Sec7 and coiled-coil domains) family. PSCD family members have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. This encoded protein is involved in the control of Golgi structure and function, and it may have a physiological role in regulating ADP-ribosylation factor protein 6 (ARF) functions, in addition to acting on ARF1. [provided by RefSeq, Jul 2008]","start":6161776,"end":6272644,"strand":-1,"description":"cytohesin 3 [Source:HGNC Symbol;Acc:HGNC:9504]"}, {"versioned_ensembl_gene_id":"ENSG00000262974.1","gene_symbol":"AC136618.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18533418,"end":18533817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282705.1","gene_symbol":"NPIPA5","gene_name":"nuclear pore complex interacting protein family member A5 [Source:HGNC Symbol;Acc:HGNC:41980]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288332","summary":null,"start":15448713,"end":15463457,"strand":-1,"description":"nuclear pore complex interacting protein family member A5 [Source:HGNC Symbol;Acc:HGNC:41980]"}, {"versioned_ensembl_gene_id":"ENSG00000226314.7","gene_symbol":"ZNF192P1","gene_name":"zinc finger protein 192 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18777]","synonyms":"ZNF389P,ZNF389,dJ265C24.4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"651302","summary":null,"start":28161781,"end":28169594,"strand":1,"description":"zinc finger protein 192 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:18777]"}, {"versioned_ensembl_gene_id":"ENSG00000232699.3","gene_symbol":"BDH2P1","gene_name":"3-hydroxybutyrate dehydrogenase 2, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21476]","synonyms":"DHRS6P1,bA758C21.1","biotype":"processed_pseudogene","ncbi_id":"389416","summary":null,"start":99174744,"end":99175479,"strand":1,"description":"3-hydroxybutyrate dehydrogenase 2, pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21476]"}, {"versioned_ensembl_gene_id":"ENSG00000253200.1","gene_symbol":"AC037459.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22613908,"end":22616657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225022.1","gene_symbol":"UBE2D3P1","gene_name":"ubiquitin conjugating enzyme E2 D3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33349]","synonyms":"UBE2D5P,UBE2D3P,RP4-680N4","biotype":"processed_pseudogene","ncbi_id":"100037280","summary":null,"start":5292388,"end":5292831,"strand":-1,"description":"ubiquitin conjugating enzyme E2 D3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33349]"}, {"versioned_ensembl_gene_id":"ENSG00000225722.1","gene_symbol":"BX890604.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3953056,"end":3953561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229519.2","gene_symbol":"AL591866.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6547905,"end":6548619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230869.1","gene_symbol":"AGAP10P","gene_name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:23659]","synonyms":"CTGLF7,CTGLF10P,bA358L16.1,bA144G6.2,AGAP10","biotype":"unprocessed_pseudogene","ncbi_id":"653234","summary":null,"start":45678692,"end":45700532,"strand":1,"description":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:23659]"}, {"versioned_ensembl_gene_id":"ENSG00000275295.1","gene_symbol":"AC073968.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45303620,"end":45304362,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122679.8","gene_symbol":"RAMP3","gene_name":"receptor activity modifying protein 3 [Source:HGNC Symbol;Acc:HGNC:9845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10268","summary":"The protein encoded by this gene is a member of the RAMP family of single-transmembrane-domain proteins, called receptor (calcitonin) activity modifying proteins (RAMPs). RAMPs are type I transmembrane proteins with an extracellular N terminus and a cytoplasmic C terminus. RAMPs are required to transport calcitonin-receptor-like receptor (CRLR) to the plasma membrane. CRLR, a receptor with seven transmembrane domains, can function as either a calcitonin-gene-related peptide (CGRP) receptor or an adrenomedullin receptor, depending on which members of the RAMP family are expressed. In the presence of this (RAMP3) protein, CRLR functions as an adrenomedullin receptor. [provided by RefSeq, Jul 2008]","start":45157791,"end":45186302,"strand":1,"description":"receptor activity modifying protein 3 [Source:HGNC Symbol;Acc:HGNC:9845]"}, {"versioned_ensembl_gene_id":"ENSG00000268120.1","gene_symbol":"AC010336.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7870561,"end":7871296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275945.1","gene_symbol":"EIF3FP1","gene_name":"eukaryotic translation initiation factor 3 subunit F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3276]","synonyms":"EIF3S5P,EIF3FP","biotype":"processed_pseudogene","ncbi_id":"54053","summary":null,"start":10330732,"end":10331537,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3276]"}, {"versioned_ensembl_gene_id":"ENSG00000243960.1","gene_symbol":"AL390195.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":111438638,"end":111441364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277693.1","gene_symbol":"AP003900.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10328411,"end":10342737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232424.1","gene_symbol":"USP9YP29","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:38765]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480425","summary":null,"start":23740258,"end":23746693,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:38765]"}, {"versioned_ensembl_gene_id":"ENSG00000116459.10","gene_symbol":"ATP5F1","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 [Source:HGNC Symbol;Acc:HGNC:840]","synonyms":null,"biotype":"protein_coding","ncbi_id":"515","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the b subunit of the proton channel. [provided by RefSeq, Jul 2008]","start":111448864,"end":111462773,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 [Source:HGNC Symbol;Acc:HGNC:840]"}, {"versioned_ensembl_gene_id":"ENSG00000203797.9","gene_symbol":"DDO","gene_name":"D-aspartate oxidase [Source:HGNC Symbol;Acc:HGNC:2727]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8528","summary":"The protein encoded by this gene is a peroxisomal flavoprotein that catalyzes the oxidative deamination of D-aspartate and N-methyl D-aspartate. Flavin adenine dinucleotide or 6-hydroxyflavin adenine dinucleotide can serve as the cofactor in this reaction. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2019]","start":110391771,"end":110415562,"strand":-1,"description":"D-aspartate oxidase [Source:HGNC Symbol;Acc:HGNC:2727]"}, {"versioned_ensembl_gene_id":"ENSG00000226816.3","gene_symbol":"AC005082.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23205787,"end":23208045,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205662.2","gene_symbol":"FAM239C","gene_name":"family with sequence similarity 239 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53416]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107987330","summary":null,"start":3929869,"end":3937855,"strand":-1,"description":"family with sequence similarity 239 member C (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:53416]"}, {"versioned_ensembl_gene_id":"ENSG00000275592.1","gene_symbol":"VN1R7P","gene_name":"vomeronasal 1 receptor 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:8496]","synonyms":"ORLP1","biotype":"processed_pseudogene","ncbi_id":"100132759","summary":null,"start":10357400,"end":10358620,"strand":1,"description":"vomeronasal 1 receptor 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:8496]"}, {"versioned_ensembl_gene_id":"ENSG00000131876.16","gene_symbol":"SNRPA1","gene_name":"small nuclear ribonucleoprotein polypeptide A' [Source:HGNC Symbol;Acc:HGNC:11152]","synonyms":"Lea1","biotype":"protein_coding","ncbi_id":"6627","summary":null,"start":101281510,"end":101295282,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide A' [Source:HGNC Symbol;Acc:HGNC:11152]"}, {"versioned_ensembl_gene_id":"ENSG00000189410.11","gene_symbol":"SH2D5","gene_name":"SH2 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28819]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400745","summary":null,"start":20719732,"end":20732837,"strand":-1,"description":"SH2 domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28819]"}, {"versioned_ensembl_gene_id":"ENSG00000261711.6","gene_symbol":"FRG2DP","gene_name":"FSHD region gene 2 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:27093]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"146481","summary":null,"start":35477414,"end":35480481,"strand":-1,"description":"FSHD region gene 2 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:27093]"}, {"versioned_ensembl_gene_id":"ENSG00000198315.10","gene_symbol":"ZKSCAN8","gene_name":"zinc finger with KRAB and SCAN domains 8 [Source:HGNC Symbol;Acc:HGNC:12983]","synonyms":"ZSCAN40,ZNF192,LD5-1","biotype":"protein_coding","ncbi_id":"7745","summary":null,"start":28141910,"end":28159472,"strand":1,"description":"zinc finger with KRAB and SCAN domains 8 [Source:HGNC Symbol;Acc:HGNC:12983]"}, {"versioned_ensembl_gene_id":"ENSG00000144214.9","gene_symbol":"LYG1","gene_name":"lysozyme g1 [Source:HGNC Symbol;Acc:HGNC:27014]","synonyms":"SALW1939","biotype":"protein_coding","ncbi_id":"129530","summary":null,"start":99284238,"end":99304742,"strand":-1,"description":"lysozyme g1 [Source:HGNC Symbol;Acc:HGNC:27014]"}, {"versioned_ensembl_gene_id":"ENSG00000182568.16","gene_symbol":"SATB1","gene_name":"SATB homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10541]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6304","summary":"This gene encodes a matrix protein which binds nuclear matrix and scaffold-associating DNAs through a unique nuclear architecture. The protein recruits chromatin-remodeling factors in order to regulate chromatin structure and gene expression. [provided by RefSeq, Apr 2016]","start":18345387,"end":18445588,"strand":-1,"description":"SATB homeobox 1 [Source:HGNC Symbol;Acc:HGNC:10541]"}, {"versioned_ensembl_gene_id":"ENSG00000245685.6","gene_symbol":"AF250324.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189780336,"end":189940271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250666.1","gene_symbol":"LINC01596","gene_name":"long intergenic non-protein coding RNA 1596 [Source:HGNC Symbol;Acc:HGNC:51591]","synonyms":"TCONS_00007705","biotype":"lincRNA","ncbi_id":"105377617","summary":null,"start":189881515,"end":189884868,"strand":1,"description":"long intergenic non-protein coding RNA 1596 [Source:HGNC Symbol;Acc:HGNC:51591]"}, {"versioned_ensembl_gene_id":"ENSG00000212712.2","gene_symbol":"AP002414.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12056676,"end":12057822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271826.5","gene_symbol":"PLS3-AS1","gene_name":"PLS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50343]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927352","summary":null,"start":115518182,"end":115562731,"strand":-1,"description":"PLS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50343]"}, {"versioned_ensembl_gene_id":"ENSG00000233141.3","gene_symbol":"MAS1L","gene_name":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]","synonyms":"dJ994E9.2,MRG,MAS-L","biotype":"protein_coding","ncbi_id":"116511","summary":null,"start":29483337,"end":29484473,"strand":-1,"description":"MAS1 proto-oncogene like, G protein-coupled receptor [Source:HGNC Symbol;Acc:HGNC:13961]"}, {"versioned_ensembl_gene_id":"ENSG00000123485.11","gene_symbol":"HJURP","gene_name":"Holliday junction recognition protein [Source:HGNC Symbol;Acc:HGNC:25444]","synonyms":"FAKTS,DKFZp762E1312,URLC9,hFLEG1","biotype":"protein_coding","ncbi_id":"55355","summary":null,"start":233833416,"end":233854566,"strand":-1,"description":"Holliday junction recognition protein [Source:HGNC Symbol;Acc:HGNC:25444]"}, {"versioned_ensembl_gene_id":"ENSG00000232625.1","gene_symbol":"RPL23AP31","gene_name":"ribosomal protein L23a pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35777]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271460","summary":null,"start":218841599,"end":218842065,"strand":1,"description":"ribosomal protein L23a pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:35777]"}, {"versioned_ensembl_gene_id":"ENSG00000267533.1","gene_symbol":"AP002414.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12067173,"end":12068417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102024.17","gene_symbol":"PLS3","gene_name":"plastin 3 [Source:HGNC Symbol;Acc:HGNC:9091]","synonyms":"T-plastin","biotype":"protein_coding","ncbi_id":"5358","summary":"Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. Plastin 1 (otherwise known as Fimbrin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has been found in all other normal cells of solid tissues that have replicative potential (fibroblasts, endothelial cells, epithelial cells, melanocytes, etc.). The C-terminal 570 amino acids of the T-plastin and L-plastin proteins are 83% identical. It contains a potential calcium-binding site near the N terminus. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]","start":115561174,"end":115650861,"strand":1,"description":"plastin 3 [Source:HGNC Symbol;Acc:HGNC:9091]"}, {"versioned_ensembl_gene_id":"ENSG00000165644.10","gene_symbol":"COMTD1","gene_name":"catechol-O-methyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26309]","synonyms":"FLJ23841","biotype":"protein_coding","ncbi_id":"118881","summary":null,"start":75233969,"end":75236030,"strand":-1,"description":"catechol-O-methyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26309]"}, {"versioned_ensembl_gene_id":"ENSG00000256616.3","gene_symbol":"AP002414.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":12073232,"end":12076654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000034053.14","gene_symbol":"APBA2","gene_name":"amyloid beta precursor protein binding family A member 2 [Source:HGNC Symbol;Acc:HGNC:579]","synonyms":"MINT2,MGC:14091,LIN-10,HsT16821,D15S1518E,X11L","biotype":"protein_coding","ncbi_id":"321","summary":"The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a putative vesicular trafficking protein in the brain that can form a complex with the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. [provided by RefSeq, Jul 2017]","start":28884483,"end":29118315,"strand":1,"description":"amyloid beta precursor protein binding family A member 2 [Source:HGNC Symbol;Acc:HGNC:579]"}, {"versioned_ensembl_gene_id":"ENSG00000124562.9","gene_symbol":"SNRPC","gene_name":"small nuclear ribonucleoprotein polypeptide C [Source:HGNC Symbol;Acc:HGNC:11157]","synonyms":"Yhc1,U1-C","biotype":"protein_coding","ncbi_id":"6631","summary":"This gene encodes one of the specific protein components of the U1 small nuclear ribonucleoprotein (snRNP) particle required for the formation of the spliceosome. The encoded protein participates in the processing of nuclear precursor messenger RNA splicing. snRNP particles are attacked by autoantibodies frequently produced by patients with connective tissue diseases. The genome contains several pseudogenes of this functional gene. Alternative splicing results in a non-coding transcript variant.[provided by RefSeq, Oct 2009]","start":34757406,"end":34773794,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide C [Source:HGNC Symbol;Acc:HGNC:11157]"}, {"versioned_ensembl_gene_id":"ENSG00000115596.3","gene_symbol":"WNT6","gene_name":"Wnt family member 6 [Source:HGNC Symbol;Acc:HGNC:12785]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7475","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line. The gene overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome 2q35 region. The protein encoded by this gene is 97% identical to the mouse Wnt6 protein at the amino acid level. [provided by RefSeq, Jul 2008]","start":218859821,"end":218874233,"strand":1,"description":"Wnt family member 6 [Source:HGNC Symbol;Acc:HGNC:12785]"}, {"versioned_ensembl_gene_id":"ENSG00000154845.15","gene_symbol":"PPP4R1","gene_name":"protein phosphatase 4 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:9320]","synonyms":"PP4R1","biotype":"protein_coding","ncbi_id":"9989","summary":"This gene encodes one of several alternate regulatory subunits of serine/threonine protein phosphatase 4 (PP4). The protein features multiple HEAT repeats. This protein forms a complex with PP4RC. This complex may have a distinct role from other PP4 complexes, including regulation of HDAC3 (Zhang et al., PMID: 15805470). There is also a transcribed pseudogene on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":9546791,"end":9615240,"strand":-1,"description":"protein phosphatase 4 regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:9320]"}, {"versioned_ensembl_gene_id":"ENSG00000251039.2","gene_symbol":"IGKV2D-40","gene_name":"immunoglobulin kappa variable 2D-40 [Source:HGNC Symbol;Acc:HGNC:5804]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28878","summary":null,"start":89851791,"end":89852497,"strand":1,"description":"immunoglobulin kappa variable 2D-40 [Source:HGNC Symbol;Acc:HGNC:5804]"}, {"versioned_ensembl_gene_id":"ENSG00000229627.2","gene_symbol":"BSNDP4","gene_name":"barttin CLCNK type accessory beta subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51539]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481726","summary":null,"start":57638725,"end":57639112,"strand":1,"description":"barttin CLCNK type accessory beta subunit pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51539]"}, {"versioned_ensembl_gene_id":"ENSG00000270749.1","gene_symbol":"AC064862.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57629285,"end":57630151,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238104.7","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"CAT53,p99,FB19,PNUTS","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30592623,"end":30610835,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000197921.5","gene_symbol":"HES5","gene_name":"hes family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:19764]","synonyms":"bHLHb38","biotype":"protein_coding","ncbi_id":"388585","summary":"This gene encodes a member of a family of basic helix-loop-helix transcriptional repressors. The protein product of this gene, which is activated downstream of the Notch pathway, regulates cell differentiation in multiple tissues. Disruptions in the normal expression of this gene have been associated with developmental diseases and cancer. [provided by RefSeq, Dec 2008]","start":2528745,"end":2530245,"strand":-1,"description":"hes family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:19764]"}, {"versioned_ensembl_gene_id":"ENSG00000254578.1","gene_symbol":"AC084125.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144463817,"end":144465101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185414.19","gene_symbol":"MRPL30","gene_name":"mitochondrial ribosomal protein L30 [Source:HGNC Symbol;Acc:HGNC:14036]","synonyms":"RPML28,MRP-L28","biotype":"protein_coding","ncbi_id":"51263","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Alternative splicing results in multiple transcript variants. Pseudogenes corresponding to this gene are found on chromosomes 6p and 12p. Read-through transcription also exists between this gene and the neighboring upstream lipoyltransferase 1 (LIPT1) gene. [provided by RefSeq, Mar 2011]","start":99181079,"end":99197626,"strand":1,"description":"mitochondrial ribosomal protein L30 [Source:HGNC Symbol;Acc:HGNC:14036]"}, {"versioned_ensembl_gene_id":"ENSG00000257400.1","gene_symbol":"AC023161.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94491546,"end":94496442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258337.1","gene_symbol":"AC130895.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":116174502,"end":116181295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257979.1","gene_symbol":"SNRPGP18","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480680","summary":null,"start":116169045,"end":116169258,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:49374]"}, {"versioned_ensembl_gene_id":"ENSG00000237941.2","gene_symbol":"KCNQ1DN","gene_name":"KCNQ1 downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13335]","synonyms":"HSA404617,BWRT","biotype":"antisense_RNA","ncbi_id":"55539","summary":"Imprinting is a phenomenon in which epigenetic modifications lead to expression or suppression of alleles of some genes based on their parental origin. Wilms tumor-2 (WT2; MIM 194071) is defined by maternal-specific loss of heterozygosity of a critical region on chromosome 11p15.5 that includes several imprinted genes. KCNQ1DN is an imprinted gene located within the WT2 critical region that is expressed from the maternal allele (Xin et al., 2000 [PubMed 11056398]).[supplied by OMIM, Mar 2008]","start":2870033,"end":2872105,"strand":1,"description":"KCNQ1 downstream neighbor (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:13335]"}, {"versioned_ensembl_gene_id":"ENSG00000260258.2","gene_symbol":"AC007346.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":52942139,"end":52943464,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281347.2","gene_symbol":"NF1P9","gene_name":"neurofibromin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51736]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101930150","summary":null,"start":21490364,"end":21509404,"strand":-1,"description":"neurofibromin 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51736]"}, {"versioned_ensembl_gene_id":"ENSG00000260939.1","gene_symbol":"AC007346.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53010395,"end":53011286,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135925.8","gene_symbol":"WNT10A","gene_name":"Wnt family member 10A [Source:HGNC Symbol;Acc:HGNC:13829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"80326","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is strongly expressed in the cell lines of promyelocytic leukemia and Burkitt's lymphoma. In addition, it and another family member, the WNT6 gene, are strongly coexpressed in colorectal cancer cell lines. The gene overexpression may play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF signaling pathway. This gene and the WNT6 gene are clustered in the chromosome 2q35 region. [provided by RefSeq, Jul 2008]","start":218880363,"end":218899581,"strand":1,"description":"Wnt family member 10A [Source:HGNC Symbol;Acc:HGNC:13829]"}, {"versioned_ensembl_gene_id":"ENSG00000258357.1","gene_symbol":"AC023161.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94521090,"end":94521869,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277639.2","gene_symbol":"AC007906.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53035690,"end":53052873,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236877.2","gene_symbol":"SETD6P1","gene_name":"SET domain containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51596]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481727","summary":null,"start":108226015,"end":108226331,"strand":-1,"description":"SET domain containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51596]"}, {"versioned_ensembl_gene_id":"ENSG00000270314.1","gene_symbol":"AC007161.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7735743,"end":7736851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279739.1","gene_symbol":"AC011369.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":168128856,"end":168130422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233108.1","gene_symbol":"AC006042.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7958183,"end":7969903,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253947.1","gene_symbol":"AC008705.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":167965187,"end":167967086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228461.1","gene_symbol":"RPL3P2","gene_name":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]","synonyms":"RPL3-Hom","biotype":"processed_pseudogene","ncbi_id":"116935","summary":null,"start":31271346,"end":31272548,"strand":1,"description":"ribosomal protein L3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17834]"}, {"versioned_ensembl_gene_id":"ENSG00000231221.1","gene_symbol":"LINC01593","gene_name":"long intergenic non-protein coding RNA 1593 [Source:HGNC Symbol;Acc:HGNC:51583]","synonyms":"TCONS_00003364","biotype":"lincRNA","ncbi_id":"107178918","summary":null,"start":108049200,"end":108052755,"strand":-1,"description":"long intergenic non-protein coding RNA 1593 [Source:HGNC Symbol;Acc:HGNC:51583]"}, {"versioned_ensembl_gene_id":"ENSG00000261866.2","gene_symbol":"AC243312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8676844,"end":8677584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236827.1","gene_symbol":"LINC00529","gene_name":"long intergenic non-protein coding RNA 529 [Source:HGNC Symbol;Acc:HGNC:15544]","synonyms":"C8orf8","biotype":"lincRNA","ncbi_id":"83647","summary":null,"start":11247626,"end":11267865,"strand":-1,"description":"long intergenic non-protein coding RNA 529 [Source:HGNC Symbol;Acc:HGNC:15544]"}, {"versioned_ensembl_gene_id":"ENSG00000064932.15","gene_symbol":"SBNO2","gene_name":"strawberry notch homolog 2 [Source:HGNC Symbol;Acc:HGNC:29158]","synonyms":"FLJ00173,Stno,Sno,KIAA0963","biotype":"protein_coding","ncbi_id":"22904","summary":null,"start":1107636,"end":1174283,"strand":-1,"description":"strawberry notch homolog 2 [Source:HGNC Symbol;Acc:HGNC:29158]"}, {"versioned_ensembl_gene_id":"ENSG00000264029.1","gene_symbol":"AC061975.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28274657,"end":28275716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138767.12","gene_symbol":"CNOT6L","gene_name":"CCR4-NOT transcription complex subunit 6 like [Source:HGNC Symbol;Acc:HGNC:18042]","synonyms":"DKFZp434K098,Ccr4b","biotype":"protein_coding","ncbi_id":"246175","summary":null,"start":77713387,"end":77819615,"strand":-1,"description":"CCR4-NOT transcription complex subunit 6 like [Source:HGNC Symbol;Acc:HGNC:18042]"}, {"versioned_ensembl_gene_id":"ENSG00000248873.1","gene_symbol":"SERBP1P6","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44635]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420450","summary":null,"start":42465400,"end":42468868,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44635]"}, {"versioned_ensembl_gene_id":"ENSG00000276582.1","gene_symbol":"ABCB11","gene_name":"ATP binding cassette subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:42]","synonyms":"BSEP,ABC16,SPGP,PGY4,PFIC2,PFIC-2","biotype":"protein_coding","ncbi_id":"8647","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008]","start":168939927,"end":168953422,"strand":-1,"description":"ATP binding cassette subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:42]"}, {"versioned_ensembl_gene_id":"ENSG00000230809.1","gene_symbol":"RPS6P15","gene_name":"ribosomal protein S6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129732","summary":null,"start":111498191,"end":111498941,"strand":-1,"description":"ribosomal protein S6 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:36942]"}, {"versioned_ensembl_gene_id":"ENSG00000227851.1","gene_symbol":"AC021035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":111349939,"end":111352103,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204352.2","gene_symbol":"C9orf129","gene_name":"chromosome 9 open reading frame 129 [Source:HGNC Symbol;Acc:HGNC:31116]","synonyms":"bA165J3.3","biotype":"protein_coding","ncbi_id":"445577","summary":null,"start":93318199,"end":93346414,"strand":-1,"description":"chromosome 9 open reading frame 129 [Source:HGNC Symbol;Acc:HGNC:31116]"}, {"versioned_ensembl_gene_id":"ENSG00000142102.15","gene_symbol":"PGGHG","gene_name":"protein-glucosylgalactosylhydroxylysine glucosidase [Source:HGNC Symbol;Acc:HGNC:26210]","synonyms":"FLJ22635,ATHL1","biotype":"protein_coding","ncbi_id":"80162","summary":null,"start":289135,"end":296107,"strand":1,"description":"protein-glucosylgalactosylhydroxylysine glucosidase [Source:HGNC Symbol;Acc:HGNC:26210]"}, {"versioned_ensembl_gene_id":"ENSG00000227227.1","gene_symbol":"AC017101.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186641339,"end":186695287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166797.10","gene_symbol":"FAM96A","gene_name":"family with sequence similarity 96 member A [Source:HGNC Symbol;Acc:HGNC:26235]","synonyms":"FLJ22875,CIA2A","biotype":"protein_coding","ncbi_id":"84191","summary":null,"start":64072559,"end":64094018,"strand":-1,"description":"family with sequence similarity 96 member A [Source:HGNC Symbol;Acc:HGNC:26235]"}, {"versioned_ensembl_gene_id":"ENSG00000170502.12","gene_symbol":"NUDT9","gene_name":"nudix hydrolase 9 [Source:HGNC Symbol;Acc:HGNC:8056]","synonyms":"MGC3037","biotype":"protein_coding","ncbi_id":"53343","summary":"The protein encoded by this gene belongs to the Nudix hydrolase family. Nudix boxes are found in a family of diverse enzymes that catalyze the hydrolysis of nucleoside diphosphate derivatives. This enzyme is an ADP-ribose pyrophosphatase that catalyzes the hydrolysis of ADP-ribose to AMP and ribose-5-P. It requires divalent metal ions and an intact Nudix motif for enzymatic activity. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":87422582,"end":87459454,"strand":1,"description":"nudix hydrolase 9 [Source:HGNC Symbol;Acc:HGNC:8056]"}, {"versioned_ensembl_gene_id":"ENSG00000254839.1","gene_symbol":"AF131215.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11062647,"end":11067089,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277850.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803411,"end":54814521,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000238088.1","gene_symbol":"OFD1P7Y","gene_name":"OFD1 pseudogene 7, Y-linked [Source:HGNC Symbol;Acc:HGNC:23879]","synonyms":"OFDYP7,OFD1PY7,OFD1P7","biotype":"unprocessed_pseudogene","ncbi_id":"386691","summary":null,"start":18848264,"end":18867280,"strand":1,"description":"OFD1 pseudogene 7, Y-linked [Source:HGNC Symbol;Acc:HGNC:23879]"}, {"versioned_ensembl_gene_id":"ENSG00000213871.3","gene_symbol":"TAF9BP1","gene_name":"TATA-box binding protein associated factor 9b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30687]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246135","summary":null,"start":25754925,"end":25755670,"strand":1,"description":"TATA-box binding protein associated factor 9b pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30687]"}, {"versioned_ensembl_gene_id":"ENSG00000184863.10","gene_symbol":"RBM33","gene_name":"RNA binding motif protein 33 [Source:HGNC Symbol;Acc:HGNC:27223]","synonyms":"PRR8,MGC20460,DKFZp686F102,DKFZp434D1319","biotype":"protein_coding","ncbi_id":"155435","summary":null,"start":155644451,"end":155781485,"strand":1,"description":"RNA binding motif protein 33 [Source:HGNC Symbol;Acc:HGNC:27223]"}, {"versioned_ensembl_gene_id":"ENSG00000264449.5","gene_symbol":"AP005433.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5887487,"end":5909122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226989.1","gene_symbol":"AL049758.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42853403,"end":42853799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233919.1","gene_symbol":"AC009743.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41162287,"end":41168547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228496.1","gene_symbol":"AC106875.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11681460,"end":11683328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104164.10","gene_symbol":"BLOC1S6","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 6 [Source:HGNC Symbol;Acc:HGNC:8549]","synonyms":"PLDN,PA,HPS9","biotype":"protein_coding","ncbi_id":"26258","summary":"The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome. [provided by RefSeq, Aug 2015]","start":45587123,"end":45615999,"strand":1,"description":"biogenesis of lysosomal organelles complex 1 subunit 6 [Source:HGNC Symbol;Acc:HGNC:8549]"}, {"versioned_ensembl_gene_id":"ENSG00000227906.7","gene_symbol":"SNAP25-AS1","gene_name":"SNAP25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44312]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100131208","summary":null,"start":10021978,"end":10368776,"strand":-1,"description":"SNAP25 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44312]"}, {"versioned_ensembl_gene_id":"ENSG00000133302.12","gene_symbol":"SLF1","gene_name":"SMC5-SMC6 complex localization factor 1 [Source:HGNC Symbol;Acc:HGNC:25408]","synonyms":"DKFZp761C121,DKFZp564C0469,BRCTx,BRCTD1,ANKRD32","biotype":"protein_coding","ncbi_id":"84250","summary":null,"start":94618347,"end":94739436,"strand":1,"description":"SMC5-SMC6 complex localization factor 1 [Source:HGNC Symbol;Acc:HGNC:25408]"}, {"versioned_ensembl_gene_id":"ENSG00000115461.4","gene_symbol":"IGFBP5","gene_name":"insulin like growth factor binding protein 5 [Source:HGNC Symbol;Acc:HGNC:5474]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3488","summary":null,"start":216672105,"end":216695525,"strand":-1,"description":"insulin like growth factor binding protein 5 [Source:HGNC Symbol;Acc:HGNC:5474]"}, {"versioned_ensembl_gene_id":"ENSG00000256101.5","gene_symbol":"AC092745.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8321876,"end":8329614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236947.5","gene_symbol":"AL139412.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156446412,"end":156456577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239397.1","gene_symbol":"AC084878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46004038,"end":46004685,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229688.7","gene_symbol":"ISPD-AS1","gene_name":"ISPD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48962]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506025","summary":null,"start":16210488,"end":16270604,"strand":1,"description":"ISPD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48962]"}, {"versioned_ensembl_gene_id":"ENSG00000277932.2","gene_symbol":"OR52E5","gene_name":"olfactory receptor family 52 subfamily E member 5 [Source:HGNC Symbol;Acc:HGNC:15214]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390082","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":5893208,"end":5902730,"strand":1,"description":"olfactory receptor family 52 subfamily E member 5 [Source:HGNC Symbol;Acc:HGNC:15214]"}, {"versioned_ensembl_gene_id":"ENSG00000100312.10","gene_symbol":"ACR","gene_name":"acrosin [Source:HGNC Symbol;Acc:HGNC:126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"49","summary":"Acrosin is the major proteinase present in the acrosome of mature spermatozoa. It is a typical serine proteinase with trypsin-like specificity. It is stored in the acrosome in its precursor form, proacrosin. The active enzyme functions in the lysis of the zona pellucida, thus facilitating penetration of the sperm through the innermost glycoprotein layers of the ovum. The mRNA for proacrosin is synthesized only in the postmeiotic stages of spermatogenesis. In humans proacrosin first appears in the haploid spermatids. [provided by RefSeq, Jul 2008]","start":50738196,"end":50745334,"strand":1,"description":"acrosin [Source:HGNC Symbol;Acc:HGNC:126]"}, {"versioned_ensembl_gene_id":"ENSG00000171502.14","gene_symbol":"COL24A1","gene_name":"collagen type XXIV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:20821]","synonyms":null,"biotype":"protein_coding","ncbi_id":"255631","summary":"This gene is a member of the collagen gene family and is thought to regulate type I collagen fibrillogenesis during fetal development. [provided by RefSeq, Mar 2017]","start":85729233,"end":86156943,"strand":-1,"description":"collagen type XXIV alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:20821]"}, {"versioned_ensembl_gene_id":"ENSG00000280002.1","gene_symbol":"AC078925.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":130988312,"end":130990028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183682.7","gene_symbol":"BMP8A","gene_name":"bone morphogenetic protein 8a [Source:HGNC Symbol;Acc:HGNC:21650]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353500","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein may play a role in development of the reproductive system. This gene may have arose from a gene duplication event and its gene duplicate is also present on chromosome 1. [provided by RefSeq, Jul 2016]","start":39491646,"end":39525935,"strand":1,"description":"bone morphogenetic protein 8a [Source:HGNC Symbol;Acc:HGNC:21650]"}, {"versioned_ensembl_gene_id":"ENSG00000279128.1","gene_symbol":"AC078925.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":131022769,"end":131024741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236185.1","gene_symbol":"HNRNPDLP3","gene_name":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48754]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481662","summary":null,"start":95610578,"end":95610957,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein D-like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48754]"}, {"versioned_ensembl_gene_id":"ENSG00000182109.7","gene_symbol":"AL365277.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39522280,"end":39546187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259369.1","gene_symbol":"AC009997.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55746639,"end":55746767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225929.1","gene_symbol":"AC000036.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50735825,"end":50738139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277589.1","gene_symbol":"AC244093.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36998598,"end":37000034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275236.1","gene_symbol":"AC009120.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74289593,"end":74291052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229379.1","gene_symbol":"AC006041.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15841297,"end":15842360,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283457.1","gene_symbol":"AC087565.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73794079,"end":73809733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278552.1","gene_symbol":"AC116165.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23225876,"end":23226391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274637.1","gene_symbol":"AC092628.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155106062,"end":155106400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232859.9","gene_symbol":"LYRM9","gene_name":"LYR motif containing 9 [Source:HGNC Symbol;Acc:HGNC:27314]","synonyms":"HSD24,C17orf108","biotype":"protein_coding","ncbi_id":"201229","summary":null,"start":27878314,"end":27894752,"strand":-1,"description":"LYR motif containing 9 [Source:HGNC Symbol;Acc:HGNC:27314]"}, {"versioned_ensembl_gene_id":"ENSG00000117614.9","gene_symbol":"SYF2","gene_name":"SYF2 pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:19824]","synonyms":"p29,NTC31,fSAP29,DKFZp564O2082,CBPIN","biotype":"protein_coding","ncbi_id":"25949","summary":"This gene encodes a nuclear protein that interacts with cyclin D-type binding-protein 1, which is thought to be a cell cycle regulator at the G1/S transition. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":25222679,"end":25232502,"strand":-1,"description":"SYF2 pre-mRNA splicing factor [Source:HGNC Symbol;Acc:HGNC:19824]"}, {"versioned_ensembl_gene_id":"ENSG00000236780.5","gene_symbol":"LINC01829","gene_name":"long intergenic non-protein coding RNA 1829 [Source:HGNC Symbol;Acc:HGNC:52635]","synonyms":null,"biotype":"lincRNA","ncbi_id":"644838","summary":null,"start":67123357,"end":67215319,"strand":-1,"description":"long intergenic non-protein coding RNA 1829 [Source:HGNC Symbol;Acc:HGNC:52635]"}, {"versioned_ensembl_gene_id":"ENSG00000139684.13","gene_symbol":"ESD","gene_name":"esterase D [Source:HGNC Symbol;Acc:HGNC:3465]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2098","summary":"This gene encodes a serine hydrolase that belongs to the esterase D family. The encoded enzyme is active toward numerous substrates including O-acetylated sialic acids, and it may be involved in the recycling of sialic acids. This gene is used as a genetic marker for retinoblastoma and Wilson's disease. [provided by RefSeq, Feb 2009]","start":46771256,"end":46797232,"strand":-1,"description":"esterase D [Source:HGNC Symbol;Acc:HGNC:3465]"}, {"versioned_ensembl_gene_id":"ENSG00000234085.1","gene_symbol":"AC064862.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":57654822,"end":57655392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185721.12","gene_symbol":"DRG1","gene_name":"developmentally regulated GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3029]","synonyms":"NEDD3","biotype":"protein_coding","ncbi_id":"4733","summary":null,"start":31399523,"end":31530634,"strand":1,"description":"developmentally regulated GTP binding protein 1 [Source:HGNC Symbol;Acc:HGNC:3029]"}, {"versioned_ensembl_gene_id":"ENSG00000215553.3","gene_symbol":"KRT18P3","gene_name":"keratin 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16540]","synonyms":"OTTHUMG00000032046,bA359G22.1","biotype":"processed_pseudogene","ncbi_id":"170527","summary":null,"start":22732802,"end":22734089,"strand":-1,"description":"keratin 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16540]"}, {"versioned_ensembl_gene_id":"ENSG00000283758.1","gene_symbol":"AC002115.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":35586260,"end":35587296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172262.11","gene_symbol":"ZNF131","gene_name":"zinc finger protein 131 [Source:HGNC Symbol;Acc:HGNC:12915]","synonyms":"ZBTB35,pHZ-10","biotype":"protein_coding","ncbi_id":"7690","summary":null,"start":43065176,"end":43192021,"strand":1,"description":"zinc finger protein 131 [Source:HGNC Symbol;Acc:HGNC:12915]"}, {"versioned_ensembl_gene_id":"ENSG00000270513.1","gene_symbol":"AC113368.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42729138,"end":42729519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253707.1","gene_symbol":"AC022616.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43284626,"end":43284806,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226425.1","gene_symbol":"AL358613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93059663,"end":93060426,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250860.1","gene_symbol":"AC093225.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42466893,"end":42468300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229072.1","gene_symbol":"HMGN2P24","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39389]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729505","summary":null,"start":40699066,"end":40699338,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:39389]"}, {"versioned_ensembl_gene_id":"ENSG00000163430.11","gene_symbol":"FSTL1","gene_name":"follistatin like 1 [Source:HGNC Symbol;Acc:HGNC:3972]","synonyms":"tsc36,OCC1,OCC-1,FSL1,FRP","biotype":"protein_coding","ncbi_id":"11167","summary":"This gene encodes a protein with similarity to follistatin, an activin-binding protein. It contains an FS module, a follistatin-like sequence containing 10 conserved cysteine residues. This gene product is thought to be an autoantigen associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]","start":120392293,"end":120451253,"strand":-1,"description":"follistatin like 1 [Source:HGNC Symbol;Acc:HGNC:3972]"}, {"versioned_ensembl_gene_id":"ENSG00000178951.8","gene_symbol":"ZBTB7A","gene_name":"zinc finger and BTB domain containing 7A [Source:HGNC Symbol;Acc:HGNC:18078]","synonyms":"ZNF857A,ZBTB7,pokemon,LRF,FBI-1,DKFZp547O146","biotype":"protein_coding","ncbi_id":"51341","summary":null,"start":4044364,"end":4066945,"strand":-1,"description":"zinc finger and BTB domain containing 7A [Source:HGNC Symbol;Acc:HGNC:18078]"}, {"versioned_ensembl_gene_id":"ENSG00000185176.12","gene_symbol":"AQP12B","gene_name":"aquaporin 12B [Source:HGNC Symbol;Acc:HGNC:6096]","synonyms":"INSSA3","biotype":"protein_coding","ncbi_id":"653437","summary":null,"start":240676418,"end":240682906,"strand":-1,"description":"aquaporin 12B [Source:HGNC Symbol;Acc:HGNC:6096]"}, {"versioned_ensembl_gene_id":"ENSG00000276004.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850300,"end":54867064,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000271682.1","gene_symbol":"AC092960.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":183462851,"end":183463201,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206460.4","gene_symbol":"CDSN","gene_name":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]","synonyms":"D6S586E","biotype":"protein_coding","ncbi_id":"1041","summary":"This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]","start":31107496,"end":31112855,"strand":-1,"description":"corneodesmosin [Source:HGNC Symbol;Acc:HGNC:1802]"}, {"versioned_ensembl_gene_id":"ENSG00000280551.1","gene_symbol":"AC096745.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":119042024,"end":119043937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134240.11","gene_symbol":"HMGCS2","gene_name":"3-hydroxy-3-methylglutaryl-CoA synthase 2 [Source:HGNC Symbol;Acc:HGNC:5008]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3158","summary":"The protein encoded by this gene belongs to the HMG-CoA synthase family. It is a mitochondrial enzyme that catalyzes the first reaction of ketogenesis, a metabolic pathway that provides lipid-derived energy for various organs during times of carbohydrate deprivation, such as fasting. Mutations in this gene are associated with HMG-CoA synthase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":119747996,"end":119768905,"strand":-1,"description":"3-hydroxy-3-methylglutaryl-CoA synthase 2 [Source:HGNC Symbol;Acc:HGNC:5008]"}, {"versioned_ensembl_gene_id":"ENSG00000227004.2","gene_symbol":"AC108032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":199872172,"end":199872378,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158089.14","gene_symbol":"GALNT14","gene_name":"polypeptide N-acetylgalactosaminyltransferase 14 [Source:HGNC Symbol;Acc:HGNC:22946]","synonyms":"GalNac-T14,GalNac-T10,FLJ12691","biotype":"protein_coding","ncbi_id":"79623","summary":"This gene encodes a Golgi protein which is a member of the polypeptide N-acetylgalactosaminyltransferase (ppGalNAc-Ts) protein family. These enzymes catalyze the transfer of N-acetyl-D-galactosamine (GalNAc) to the hydroxyl groups on serines and threonines in target peptides. The encoded protein has been shown to transfer GalNAc to large proteins like mucins. Alterations in this gene may play a role in cancer progression and response to chemotherapy. [provided by RefSeq, Jun 2016]","start":30910467,"end":31155202,"strand":-1,"description":"polypeptide N-acetylgalactosaminyltransferase 14 [Source:HGNC Symbol;Acc:HGNC:22946]"}, {"versioned_ensembl_gene_id":"ENSG00000281944.1","gene_symbol":"IGHV3-6","gene_name":"immunoglobulin heavy variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5613]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28453","summary":null,"start":106056320,"end":106056769,"strand":-1,"description":"immunoglobulin heavy variable 3-6 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5613]"}, {"versioned_ensembl_gene_id":"ENSG00000233336.1","gene_symbol":"AC245056.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13146981,"end":13147460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260071.1","gene_symbol":"AC007221.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9466655,"end":9517564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261397.1","gene_symbol":"LINC01177","gene_name":"long intergenic non-protein coding RNA 1177 [Source:HGNC Symbol;Acc:HGNC:49549]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355218","summary":null,"start":9441294,"end":9444985,"strand":-1,"description":"long intergenic non-protein coding RNA 1177 [Source:HGNC Symbol;Acc:HGNC:49549]"}, {"versioned_ensembl_gene_id":"ENSG00000226124.6","gene_symbol":"FTCDNL1","gene_name":"formiminotransferase cyclodeaminase N-terminal like [Source:HGNC Symbol;Acc:HGNC:48661]","synonyms":"FONG","biotype":"protein_coding","ncbi_id":"348751","summary":null,"start":199760544,"end":199851173,"strand":-1,"description":"formiminotransferase cyclodeaminase N-terminal like [Source:HGNC Symbol;Acc:HGNC:48661]"}, {"versioned_ensembl_gene_id":"ENSG00000175505.10","gene_symbol":"CLCF1","gene_name":"cardiotrophin like cytokine factor 1 [Source:HGNC Symbol;Acc:HGNC:17412]","synonyms":"NR6,NNT1,NNT-1,CLC,CISS2,BSF3,BSF-3","biotype":"protein_coding","ncbi_id":"23529","summary":"This gene is a member of the glycoprotein (gp)130 cytokine family and encodes cardiotrophin-like cytokine factor 1 (CLCF1). CLCF1 forms a heterodimer complex with cytokine receptor-like factor 1 (CRLF1). This dimer competes with ciliary neurotrophic factor (CNTF) for binding to the ciliary neurotrophic factor receptor (CNTFR) complex, and activates the Jak-STAT signaling cascade. CLCF1 can be actively secreted from cells by forming a complex with soluble type I CRLF1 or soluble CNTFR. CLCF1 is a potent neurotrophic factor, B-cell stimulatory agent and neuroendocrine modulator of pituitary corticotroph function. Defects in CLCF1 cause cold-induced sweating syndrome 2 (CISS2). This syndrome is characterized by a profuse sweating after exposure to cold as well as congenital physical abnormalities of the head and spine. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]","start":67364168,"end":67374177,"strand":-1,"description":"cardiotrophin like cytokine factor 1 [Source:HGNC Symbol;Acc:HGNC:17412]"}, {"versioned_ensembl_gene_id":"ENSG00000256514.1","gene_symbol":"AP003419.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":67351572,"end":67373584,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175697.10","gene_symbol":"GPR156","gene_name":"G protein-coupled receptor 156 [Source:HGNC Symbol;Acc:HGNC:20844]","synonyms":"PGR28,GABABL","biotype":"protein_coding","ncbi_id":"165829","summary":"G protein-coupled receptors (GPCRs) are a large superfamily of cell surface receptors characterized by 7 helical transmembrane domains, together with N-terminal extracellular and C-terminal intracellular domains.[supplied by OMIM, Mar 2008]","start":120164645,"end":120285094,"strand":-1,"description":"G protein-coupled receptor 156 [Source:HGNC Symbol;Acc:HGNC:20844]"}, {"versioned_ensembl_gene_id":"ENSG00000274384.4","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160592,"end":54173661,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000244167.1","gene_symbol":"AC005532.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7177952,"end":7178324,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261184.1","gene_symbol":"AC083864.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":36095272,"end":36100653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242100.2","gene_symbol":"RPL9P32","gene_name":"ribosomal protein L9 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36418]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"727865","summary":null,"start":29956369,"end":29956988,"strand":-1,"description":"ribosomal protein L9 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36418]"}, {"versioned_ensembl_gene_id":"ENSG00000244619.2","gene_symbol":"AC243547.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":145892847,"end":145893483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139218.17","gene_symbol":"SCAF11","gene_name":"SR-related CTD associated factor 11 [Source:HGNC Symbol;Acc:HGNC:10784]","synonyms":"SRSF2IP,SRRP129,SIP1,SFRS2IP,CASP11","biotype":"protein_coding","ncbi_id":"9169","summary":null,"start":45919131,"end":45992120,"strand":-1,"description":"SR-related CTD associated factor 11 [Source:HGNC Symbol;Acc:HGNC:10784]"}, {"versioned_ensembl_gene_id":"ENSG00000060138.12","gene_symbol":"YBX3","gene_name":"Y-box binding protein 3 [Source:HGNC Symbol;Acc:HGNC:2428]","synonyms":"ZONAB,dbpA,CSDA1,CSDA","biotype":"protein_coding","ncbi_id":"8531","summary":null,"start":10699089,"end":10723312,"strand":-1,"description":"Y-box binding protein 3 [Source:HGNC Symbol;Acc:HGNC:2428]"}, {"versioned_ensembl_gene_id":"ENSG00000152952.11","gene_symbol":"PLOD2","gene_name":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:9082]","synonyms":"LH2","biotype":"protein_coding","ncbi_id":"5352","summary":"The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. Mutations in the coding region of this gene are associated with Bruck syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":146069440,"end":146163653,"strand":-1,"description":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 [Source:HGNC Symbol;Acc:HGNC:9082]"}, {"versioned_ensembl_gene_id":"ENSG00000227055.1","gene_symbol":"AC009961.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":159812234,"end":159814009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196796.5","gene_symbol":"NPIPB10P","gene_name":"nuclear pore complex interacting protein family, member B10, pseudogene [Source:HGNC Symbol;Acc:HGNC:37455]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"730153","summary":null,"start":29038655,"end":29052726,"strand":1,"description":"nuclear pore complex interacting protein family, member B10, pseudogene [Source:HGNC Symbol;Acc:HGNC:37455]"}, {"versioned_ensembl_gene_id":"ENSG00000084463.7","gene_symbol":"WBP11","gene_name":"WW domain binding protein 11 [Source:HGNC Symbol;Acc:HGNC:16461]","synonyms":"SIPP1,PPP1R165,NPWBP","biotype":"protein_coding","ncbi_id":"51729","summary":"This gene encodes a nuclear protein, which colocalizes with mRNA splicing factors and intermediate filament-containing perinuclear networks. This protein has 95% amino acid sequence identity to the mouse Wbp11 protein. It contains two proline-rich regions that bind to the WW domain of Npw38, a nuclear protein, and thus this protein is also called Npw38-binding protein NpwBP. The Npw38-NpwBP complex may function as a component of an mRNA factory in the nucleus. [provided by RefSeq, Jul 2008]","start":14784579,"end":14803540,"strand":-1,"description":"WW domain binding protein 11 [Source:HGNC Symbol;Acc:HGNC:16461]"}, {"versioned_ensembl_gene_id":"ENSG00000166363.5","gene_symbol":"OR10A5","gene_name":"olfactory receptor family 10 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:15131]","synonyms":"OR11-403,OR10A1,JCG6","biotype":"protein_coding","ncbi_id":"144124","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6845652,"end":6846705,"strand":1,"description":"olfactory receptor family 10 subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:15131]"}, {"versioned_ensembl_gene_id":"ENSG00000275156.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54914255,"end":54924255,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000170790.5","gene_symbol":"OR10A2","gene_name":"olfactory receptor family 10 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8161]","synonyms":"OST363,OR10A2P","biotype":"protein_coding","ncbi_id":"341276","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":6863057,"end":6874717,"strand":1,"description":"olfactory receptor family 10 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:8161]"}, {"versioned_ensembl_gene_id":"ENSG00000281797.1","gene_symbol":"AC139677.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46799540,"end":46804933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214711.9","gene_symbol":"CAPN14","gene_name":"calpain 14 [Source:HGNC Symbol;Acc:HGNC:16664]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440854","summary":"Calpains are a family of cytosolic calcium-activated cysteine proteases involved in a variety of cellular processes including apoptosis, cell division, modulation of integrin-cytoskeletal interactions, and synaptic plasticity (Dear et al., 2000 [PubMed 10964513]). CAPN14 belongs to the calpain large subunit family.[supplied by OMIM, Mar 2008]","start":31173056,"end":31233858,"strand":-1,"description":"calpain 14 [Source:HGNC Symbol;Acc:HGNC:16664]"}, {"versioned_ensembl_gene_id":"ENSG00000274382.2","gene_symbol":"PROP1","gene_name":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5626","summary":"This gene encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Expression occurs prior to and is required for expression of pou domain transcription factor 1, which is responsible for pituitary development and hormone expression. Mutations in this gene have been associated with combined pituitary hormone deficiency-2 as well as deficiencies in luteinizing hormone, follicle-stimulating hormone, growth hormone, prolactin, and thyroid-stimulating hormone. [provided by RefSeq, Sep 2011]","start":177992545,"end":177996421,"strand":-1,"description":"PROP paired-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9455]"}, {"versioned_ensembl_gene_id":"ENSG00000185156.5","gene_symbol":"MFSD6L","gene_name":"major facilitator superfamily domain containing 6 like [Source:HGNC Symbol;Acc:HGNC:26656]","synonyms":"FLJ35773","biotype":"protein_coding","ncbi_id":"162387","summary":null,"start":8797162,"end":8799349,"strand":-1,"description":"major facilitator superfamily domain containing 6 like [Source:HGNC Symbol;Acc:HGNC:26656]"}, {"versioned_ensembl_gene_id":"ENSG00000163914.4","gene_symbol":"RHO","gene_name":"rhodopsin [Source:HGNC Symbol;Acc:HGNC:10012]","synonyms":"CSNBAD1,RP4,OPN2","biotype":"protein_coding","ncbi_id":"6010","summary":"The protein encoded by this gene is found in rod cells in the back of the eye and is essential for vision in low-light conditions. The encoded protein binds to 11-cis retinal and is activated when light hits the retinal molecule. Defects in this gene are a cause of congenital stationary night blindness. [provided by RefSeq, Aug 2017]","start":129528640,"end":129535169,"strand":1,"description":"rhodopsin [Source:HGNC Symbol;Acc:HGNC:10012]"}, {"versioned_ensembl_gene_id":"ENSG00000267664.1","gene_symbol":"RPL17P45","gene_name":"ribosomal protein L17 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271414","summary":null,"start":40143926,"end":40144504,"strand":-1,"description":"ribosomal protein L17 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:35618]"}, {"versioned_ensembl_gene_id":"ENSG00000238225.1","gene_symbol":"CRIP1P2","gene_name":"cysteine rich protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44517]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"641456","summary":null,"start":25686896,"end":25687123,"strand":1,"description":"cysteine rich protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44517]"}, {"versioned_ensembl_gene_id":"ENSG00000177519.3","gene_symbol":"RPRM","gene_name":"reprimo, TP53 dependent G2 arrest mediator homolog [Source:HGNC Symbol;Acc:HGNC:24201]","synonyms":"REPRIMO,FLJ90327","biotype":"protein_coding","ncbi_id":"56475","summary":null,"start":153477338,"end":153478808,"strand":-1,"description":"reprimo, TP53 dependent G2 arrest mediator homolog [Source:HGNC Symbol;Acc:HGNC:24201]"}, {"versioned_ensembl_gene_id":"ENSG00000164849.9","gene_symbol":"GPR146","gene_name":"G protein-coupled receptor 146 [Source:HGNC Symbol;Acc:HGNC:21718]","synonyms":"PGR8","biotype":"protein_coding","ncbi_id":"115330","summary":null,"start":1044576,"end":1059261,"strand":1,"description":"G protein-coupled receptor 146 [Source:HGNC Symbol;Acc:HGNC:21718]"}, {"versioned_ensembl_gene_id":"ENSG00000205268.10","gene_symbol":"PDE7A","gene_name":"phosphodiesterase 7A [Source:HGNC Symbol;Acc:HGNC:8791]","synonyms":"HCP1","biotype":"protein_coding","ncbi_id":"5150","summary":"The protein encoded by this gene belongs to the cyclic nucleotide phosphodiesterase (PDE) family, and PDE7 subfamily. This PDE hydrolyzes the second messenger, cAMP, which is a regulator and mediator of a number of cellular responses to extracellular signals. Thus, by regulating the cellular concentration of cAMP, this protein plays a key role in many important physiological processes. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2011]","start":65717510,"end":65842322,"strand":-1,"description":"phosphodiesterase 7A [Source:HGNC Symbol;Acc:HGNC:8791]"}, {"versioned_ensembl_gene_id":"ENSG00000238067.1","gene_symbol":"XKRYP1","gene_name":"XK related, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23908]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379028","summary":null,"start":18508577,"end":18509068,"strand":1,"description":"XK related, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23908]"}, {"versioned_ensembl_gene_id":"ENSG00000250951.1","gene_symbol":"USP9YP1","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31741]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387362","summary":null,"start":18540980,"end":18544128,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31741]"}, {"versioned_ensembl_gene_id":"ENSG00000131007.9","gene_symbol":"TTTY9B","gene_name":"testis-specific transcript, Y-linked 9B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32425]","synonyms":"NCRNA00132","biotype":"antisense_RNA","ncbi_id":"425057","summary":"This gene is transcribed but does not appear to encode a protein. Two identical copies of this gene are present in a palindromic region (P4) on chromosome Y. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":18581206,"end":18590521,"strand":-1,"description":"testis-specific transcript, Y-linked 9B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32425]"}, {"versioned_ensembl_gene_id":"ENSG00000226680.2","gene_symbol":"AC073311.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123069249,"end":123103589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279507.1","gene_symbol":"AC112484.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":128914833,"end":128915060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274191.1","gene_symbol":"AC026333.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122634130,"end":122634673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170011.13","gene_symbol":"MYRIP","gene_name":"myosin VIIA and Rab interacting protein [Source:HGNC Symbol;Acc:HGNC:19156]","synonyms":"exophilin-8,DKFZp586F1018,SLAC2C,SLAC2-C,MyRIP","biotype":"protein_coding","ncbi_id":"25924","summary":null,"start":39808914,"end":40260321,"strand":1,"description":"myosin VIIA and Rab interacting protein [Source:HGNC Symbol;Acc:HGNC:19156]"}, {"versioned_ensembl_gene_id":"ENSG00000104218.14","gene_symbol":"CSPP1","gene_name":"centrosome and spindle pole associated protein 1 [Source:HGNC Symbol;Acc:HGNC:26193]","synonyms":"JBTS21,FLJ22490,CSPP","biotype":"protein_coding","ncbi_id":"79848","summary":"This gene encodes a centrosome and spindle pole associated protein. The encoded protein plays a role in cell-cycle progression and spindle organization, regulates cytokinesis, interacts with Nephrocystin 8 and is required for cilia formation. Mutations in this gene result in primary cilia abnormalities and classical Joubert syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Apr 2014]","start":67062426,"end":67196263,"strand":1,"description":"centrosome and spindle pole associated protein 1 [Source:HGNC Symbol;Acc:HGNC:26193]"}, {"versioned_ensembl_gene_id":"ENSG00000267675.1","gene_symbol":"AC105105.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58416765,"end":58417628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138688.15","gene_symbol":"KIAA1109","gene_name":"KIAA1109 [Source:HGNC Symbol;Acc:HGNC:26953]","synonyms":"Tweek,KIAA1371,FSA,FLJ21404","biotype":"protein_coding","ncbi_id":"84162","summary":"This gene is located on the long arm of chromosome 4 in a region that is associated with susceptibility to celiac disease. The encoded protein is similar to a Chinese hamster protein that is associated with spermatocyte and adipocyte differentiation. The C-terminus of the protein is also similar to a Caenorhabditis elegans protein that plays a role in lipid storage. In mammals, this protein is thought to function in the regulation of epithelial growth and differentiation, and in tumor development. [provided by RefSeq, Oct 2009]","start":122152333,"end":122362758,"strand":1,"description":"KIAA1109 [Source:HGNC Symbol;Acc:HGNC:26953]"}, {"versioned_ensembl_gene_id":"ENSG00000184111.6","gene_symbol":"RPL11P4","gene_name":"ribosomal protein L11 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36137]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271272","summary":null,"start":92596852,"end":92597287,"strand":-1,"description":"ribosomal protein L11 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36137]"}, {"versioned_ensembl_gene_id":"ENSG00000275583.5","gene_symbol":"CU464060.1","gene_name":"Killer cell immunoglobulin-like receptor 2DS2 [Source:UniProtKB/Swiss-Prot;Acc:P43631]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54746804,"end":54761173,"strand":1,"description":"Killer cell immunoglobulin-like receptor 2DS2 [Source:UniProtKB/Swiss-Prot;Acc:P43631]"}, {"versioned_ensembl_gene_id":"ENSG00000278572.1","gene_symbol":"AL355877.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26218581,"end":26220476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226943.3","gene_symbol":"ALG1L5P","gene_name":"asparagine-linked glycosylation 1-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:44374]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"647415","summary":null,"start":6923804,"end":6930835,"strand":1,"description":"asparagine-linked glycosylation 1-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:44374]"}, {"versioned_ensembl_gene_id":"ENSG00000274921.2","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54763075,"end":54854081,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000188738.14","gene_symbol":"FSIP2","gene_name":"fibrous sheath interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:21675]","synonyms":"FLJ34780","biotype":"protein_coding","ncbi_id":"401024","summary":"This gene encodes a protein associated with the sperm fibrous sheath. Genes encoding most of the fibrous-sheath associated proteins genes are transcribed only during the postmeiotic period of spermatogenesis. The protein encoded by this gene is specific to spermatogenic cells. Copy number variation in this gene may be associated with testicular germ cell tumors. Pseudogenes associated with this gene are reported on chromosomes 2 and X. [provided by RefSeq, Aug 2016]","start":185738895,"end":185833290,"strand":1,"description":"fibrous sheath interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:21675]"}, {"versioned_ensembl_gene_id":"ENSG00000256197.1","gene_symbol":"TSPAN9-IT1","gene_name":"TSPAN9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41462]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874356","summary":null,"start":3149797,"end":3151476,"strand":1,"description":"TSPAN9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41462]"}, {"versioned_ensembl_gene_id":"ENSG00000274498.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54779616,"end":54785052,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000182600.9","gene_symbol":"C2orf82","gene_name":"chromosome 2 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:33763]","synonyms":"UNQ830,ASCL830","biotype":"protein_coding","ncbi_id":"389084","summary":null,"start":232857270,"end":232878708,"strand":1,"description":"chromosome 2 open reading frame 82 [Source:HGNC Symbol;Acc:HGNC:33763]"}, {"versioned_ensembl_gene_id":"ENSG00000241409.1","gene_symbol":"AC064852.1","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":232760146,"end":232767949,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276689.1","gene_symbol":"AL450487.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65786763,"end":65787169,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278780.4","gene_symbol":"ZNF430","gene_name":"zinc finger protein 430 [Source:HGNC Symbol;Acc:HGNC:20808]","synonyms":"FLJ13659","biotype":"protein_coding","ncbi_id":"80264","summary":null,"start":21027036,"end":21043218,"strand":1,"description":"zinc finger protein 430 [Source:HGNC Symbol;Acc:HGNC:20808]"}, {"versioned_ensembl_gene_id":"ENSG00000113593.11","gene_symbol":"PPWD1","gene_name":"peptidylprolyl isomerase domain and WD repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:28954]","synonyms":"KIAA0073","biotype":"protein_coding","ncbi_id":"23398","summary":null,"start":65563236,"end":65587549,"strand":1,"description":"peptidylprolyl isomerase domain and WD repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:28954]"}, {"versioned_ensembl_gene_id":"ENSG00000272391.5","gene_symbol":"POM121C","gene_name":"POM121 transmembrane nucleoporin C [Source:HGNC Symbol;Acc:HGNC:34005]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100101267","summary":null,"start":75416787,"end":75486271,"strand":-1,"description":"POM121 transmembrane nucleoporin C [Source:HGNC Symbol;Acc:HGNC:34005]"}, {"versioned_ensembl_gene_id":"ENSG00000139223.2","gene_symbol":"ANP32D","gene_name":"acidic nuclear phosphoprotein 32 family member D [Source:HGNC Symbol;Acc:HGNC:16676]","synonyms":"PP32R2","biotype":"protein_coding","ncbi_id":"23519","summary":"Phosphoprotein 32 (PP32) is a tumor suppressor that can inhibit several types of cancers, including prostate and breast cancers. The protein encoded by this gene is one of at least two proteins that are similar in amino acid sequence to PP32 and are part of the same acidic nuclear phosphoprotein gene family. However, unlike PP32, the encoded protein is tumorigenic. The tumor suppressor function of PP32 has been localized to a 25 amino acid region that is absent in the protein encoded by this gene. This gene does not contain introns. [provided by RefSeq, Jul 2008]","start":48472665,"end":48473624,"strand":1,"description":"acidic nuclear phosphoprotein 32 family member D [Source:HGNC Symbol;Acc:HGNC:16676]"}, {"versioned_ensembl_gene_id":"ENSG00000178761.14","gene_symbol":"FAM219B","gene_name":"family with sequence similarity 219 member B [Source:HGNC Symbol;Acc:HGNC:24695]","synonyms":"FLJ00005,C15orf17","biotype":"protein_coding","ncbi_id":"57184","summary":null,"start":74899987,"end":74907121,"strand":-1,"description":"family with sequence similarity 219 member B [Source:HGNC Symbol;Acc:HGNC:24695]"}, {"versioned_ensembl_gene_id":"ENSG00000259639.5","gene_symbol":"AC021351.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35939167,"end":36252257,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230275.2","gene_symbol":"SERBP1P4","gene_name":"SERPINE1 mRNA binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44631]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132591","summary":null,"start":91560436,"end":91561597,"strand":-1,"description":"SERPINE1 mRNA binding protein 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44631]"}, {"versioned_ensembl_gene_id":"ENSG00000259245.1","gene_symbol":"AC040918.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36046082,"end":36049529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276874.1","gene_symbol":"AC011718.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18374106,"end":18375689,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000118762.7","gene_symbol":"PKD2","gene_name":"polycystin 2, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9009]","synonyms":"TRPP2,PKD4,PC2,Pc-2","biotype":"protein_coding","ncbi_id":"5311","summary":"This gene encodes a member of the polycystin protein family. The encoded protein is a multi-pass membrane protein that functions as a calcium permeable cation channel, and is involved in calcium transport and calcium signaling in renal epithelial cells. This protein interacts with polycystin 1, and they may be partners in a common signaling cascade involved in tubular morphogenesis. Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2. [provided by RefSeq, Mar 2011]","start":88007668,"end":88077777,"strand":1,"description":"polycystin 2, transient receptor potential cation channel [Source:HGNC Symbol;Acc:HGNC:9009]"}, {"versioned_ensembl_gene_id":"ENSG00000276739.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54857994,"end":54874788,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000178802.17","gene_symbol":"MPI","gene_name":"mannose phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:7216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4351","summary":"Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":74890005,"end":74902219,"strand":1,"description":"mannose phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:7216]"}, {"versioned_ensembl_gene_id":"ENSG00000070087.13","gene_symbol":"PFN2","gene_name":"profilin 2 [Source:HGNC Symbol;Acc:HGNC:8882]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5217","summary":"The protein encoded by this gene is a ubiquitous actin monomer-binding protein belonging to the profilin family. It is thought to regulate actin polymerization in response to extracellular signals. There are two alternatively spliced transcript variants encoding different isoforms described for this gene. [provided by RefSeq, Jul 2008]","start":149964904,"end":150050788,"strand":-1,"description":"profilin 2 [Source:HGNC Symbol;Acc:HGNC:8882]"}, {"versioned_ensembl_gene_id":"ENSG00000060140.8","gene_symbol":"STYK1","gene_name":"serine/threonine/tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18889]","synonyms":"SuRTK106,NOK,DKFZp761P1010","biotype":"protein_coding","ncbi_id":"55359","summary":"Receptor protein tyrosine kinases, like STYK1, play important roles in diverse cellular and developmental processes, such as cell proliferation, differentiation, and survival (Liu et al., 2004 [PubMed 15150103]).[supplied by OMIM, Mar 2008]","start":10618939,"end":10674318,"strand":-1,"description":"serine/threonine/tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:18889]"}, {"versioned_ensembl_gene_id":"ENSG00000249212.1","gene_symbol":"ATP1B1P1","gene_name":"ATPase Na+/K+ transporting subunit beta 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:809]","synonyms":"ATP1BL1","biotype":"unprocessed_pseudogene","ncbi_id":"485","summary":null,"start":42029209,"end":42030123,"strand":1,"description":"ATPase Na+/K+ transporting subunit beta 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:809]"}, {"versioned_ensembl_gene_id":"ENSG00000281150.1","gene_symbol":"FAM90A21P","gene_name":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"619418","summary":null,"start":7556326,"end":7559336,"strand":-1,"description":"family with sequence similarity 90 member A21, pseudogene [Source:HGNC Symbol;Acc:HGNC:32269]"}, {"versioned_ensembl_gene_id":"ENSG00000103375.10","gene_symbol":"AQP8","gene_name":"aquaporin 8 [Source:HGNC Symbol;Acc:HGNC:642]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343","summary":"Aquaporin 8 (AQP8) is a water channel protein. Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein (MIP or AQP0). Aquaporin 8 mRNA is found in pancreas and colon but not other tissues. [provided by RefSeq, Jul 2008]","start":25215731,"end":25228940,"strand":1,"description":"aquaporin 8 [Source:HGNC Symbol;Acc:HGNC:642]"}, {"versioned_ensembl_gene_id":"ENSG00000225716.1","gene_symbol":"ELOCP13","gene_name":"elongin C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38149]","synonyms":"TCEB1P13","biotype":"processed_pseudogene","ncbi_id":"100462875","summary":null,"start":18440797,"end":18441125,"strand":1,"description":"elongin C pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:38149]"}, {"versioned_ensembl_gene_id":"ENSG00000166341.7","gene_symbol":"DCHS1","gene_name":"dachsous cadherin-related 1 [Source:HGNC Symbol;Acc:HGNC:13681]","synonyms":"PCDH16,KIAA1773,FLJ11790,FIB1,CDHR6,CDH25","biotype":"protein_coding","ncbi_id":"8642","summary":"This gene is a member of the cadherin superfamily whose members encode calcium-dependent cell-cell adhesion molecules. The encoded protein has a signal peptide, 27 cadherin repeat domains and a unique cytoplasmic region. This particular cadherin family member is expressed in fibroblasts but not in melanocytes or keratinocytes. The cell-cell adhesion of fibroblasts is thought to be necessary for wound healing. [provided by RefSeq, Jul 2008]","start":6621323,"end":6655854,"strand":-1,"description":"dachsous cadherin-related 1 [Source:HGNC Symbol;Acc:HGNC:13681]"}, {"versioned_ensembl_gene_id":"ENSG00000240888.1","gene_symbol":"AC131210.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":143313067,"end":143314429,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223590.5","gene_symbol":"MUC21","gene_name":"mucin 21, cell surface associated [Source:NCBI gene;Acc:394263]","synonyms":"C6orf205,C6orf205,MUC-21,C6orf205,bCX31G15.2,KMQK697,bCX31G15.2","biotype":"protein_coding","ncbi_id":"394263","summary":"This gene encodes a large membrane-bound glycoprotein which is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with isoforms containing a variable number of nonidentical proline-, threonine-, and serine-rich tandem repeats of 15 amino acids each. The aberrent expression of this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]","start":31028368,"end":31034648,"strand":1,"description":"mucin 21, cell surface associated [Source:NCBI gene;Acc:394263]"}, {"versioned_ensembl_gene_id":"ENSG00000226362.2","gene_symbol":"FAM41AY2","gene_name":"family with sequence similarity 41 member A, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:37135]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100302526","summary":null,"start":18390994,"end":18405046,"strand":-1,"description":"family with sequence similarity 41 member A, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:37135]"}, {"versioned_ensembl_gene_id":"ENSG00000184144.11","gene_symbol":"CNTN2","gene_name":"contactin 2 [Source:HGNC Symbol;Acc:HGNC:2172]","synonyms":"TAX1,TAX,TAG-1,AXT","biotype":"protein_coding","ncbi_id":"6900","summary":"This gene encodes a member of the contactin family of proteins, part of the immunoglobulin superfamily of cell adhesion molecules. The encoded glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein plays a role in the proliferation, migration, and axon guidance of neurons of the developing cerebellum. A mutation in this gene may be associated with adult myoclonic epilepsy. [provided by RefSeq, Sep 2016]","start":205042937,"end":205078284,"strand":1,"description":"contactin 2 [Source:HGNC Symbol;Acc:HGNC:2172]"}, {"versioned_ensembl_gene_id":"ENSG00000226199.1","gene_symbol":"AC112492.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27832175,"end":27833204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271727.1","gene_symbol":"AL357054.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":711533,"end":750729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267707.2","gene_symbol":"AC015961.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37243776,"end":37247506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177042.14","gene_symbol":"TMEM80","gene_name":"transmembrane protein 80 [Source:HGNC Symbol;Acc:HGNC:27453]","synonyms":"FLJ38216","biotype":"protein_coding","ncbi_id":"283232","summary":null,"start":695428,"end":705028,"strand":1,"description":"transmembrane protein 80 [Source:HGNC Symbol;Acc:HGNC:27453]"}, {"versioned_ensembl_gene_id":"ENSG00000189186.10","gene_symbol":"DCAF8L2","gene_name":"DDB1 and CUL4 associated factor 8 like 2 [Source:HGNC Symbol;Acc:HGNC:31811]","synonyms":"WDR42C","biotype":"protein_coding","ncbi_id":"347442","summary":null,"start":27590382,"end":27748821,"strand":1,"description":"DDB1 and CUL4 associated factor 8 like 2 [Source:HGNC Symbol;Acc:HGNC:31811]"}, {"versioned_ensembl_gene_id":"ENSG00000204510.5","gene_symbol":"PRAMEF7","gene_name":"PRAME family member 7 [Source:HGNC Symbol;Acc:HGNC:28415]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441871","summary":null,"start":12916610,"end":12920482,"strand":1,"description":"PRAME family member 7 [Source:HGNC Symbol;Acc:HGNC:28415]"}, {"versioned_ensembl_gene_id":"ENSG00000240592.5","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"C6orf8,NG3","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32241011,"end":32244709,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000276337.1","gene_symbol":"AC105429.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":87470370,"end":87474370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225024.1","gene_symbol":"AC015977.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26678219,"end":26678510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187545.5","gene_symbol":"PRAMEF10","gene_name":"PRAME family member 10 [Source:HGNC Symbol;Acc:HGNC:27997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343071","summary":null,"start":12892896,"end":12898270,"strand":-1,"description":"PRAME family member 10 [Source:HGNC Symbol;Acc:HGNC:27997]"}, {"versioned_ensembl_gene_id":"ENSG00000225378.1","gene_symbol":"AC015977.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26671254,"end":26674464,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134759.13","gene_symbol":"ELP2","gene_name":"elongator acetyltransferase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:18248]","synonyms":"STATIP1,FLJ10879,StIP","biotype":"protein_coding","ncbi_id":"55250","summary":"The protein encoded by this gene is a core subunit of the elongator complex, a histone acetyltransferase complex that associates with RNA polymerase II. In addition to histone acetylation, the encoded protein effects transcriptional elongation and may help remodel chromatin. [provided by RefSeq, May 2016]","start":36129444,"end":36180556,"strand":1,"description":"elongator acetyltransferase complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:18248]"}, {"versioned_ensembl_gene_id":"ENSG00000158014.14","gene_symbol":"SLC30A2","gene_name":"solute carrier family 30 member 2 [Source:HGNC Symbol;Acc:HGNC:11013]","synonyms":"ZNT2","biotype":"protein_coding","ncbi_id":"7780","summary":"The protein encoded by this gene is a zinc transporter that acts as a homodimer. The encoded protein plays a role in secreting zinc into breast milk. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":26037252,"end":26046133,"strand":-1,"description":"solute carrier family 30 member 2 [Source:HGNC Symbol;Acc:HGNC:11013]"}, {"versioned_ensembl_gene_id":"ENSG00000101199.12","gene_symbol":"ARFGAP1","gene_name":"ADP ribosylation factor GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:15852]","synonyms":"FLJ10767,bA261N11.3,ARF1GAP","biotype":"protein_coding","ncbi_id":"55738","summary":"The protein encoded by this gene is a GTPase-activating protein, which associates with the Golgi apparatus and which interacts with ADP-ribosylation factor 1. The encoded protein promotes hydrolysis of ADP-ribosylation factor 1-bound GTP and is required for the dissociation of coat proteins from Golgi-derived membranes and vesicles. Dissociation of the coat proteins is required for the fusion of these vesicles with target compartments. The activity of this protein is stimulated by phosphoinosides and inhibited by phosphatidylcholine. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":63272785,"end":63289793,"strand":1,"description":"ADP ribosylation factor GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:15852]"}, {"versioned_ensembl_gene_id":"ENSG00000223553.6","gene_symbol":"SMPD4P1","gene_name":"sphingomyelin phosphodiesterase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39673]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645280","summary":null,"start":20602595,"end":20656914,"strand":-1,"description":"sphingomyelin phosphodiesterase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39673]"}, {"versioned_ensembl_gene_id":"ENSG00000232884.7","gene_symbol":"AF127936.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14746762,"end":14753863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280063.1","gene_symbol":"AC012676.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":4346694,"end":4348648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261008.6","gene_symbol":"LINC01572","gene_name":"long intergenic non-protein coding RNA 1572 [Source:HGNC Symbol;Acc:HGNC:51385]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927957","summary":null,"start":72283301,"end":72665009,"strand":-1,"description":"long intergenic non-protein coding RNA 1572 [Source:HGNC Symbol;Acc:HGNC:51385]"}, {"versioned_ensembl_gene_id":"ENSG00000260664.2","gene_symbol":"AC004158.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72425948,"end":72533892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224960.4","gene_symbol":"PPP4R3CP","gene_name":"protein phosphatase 4 regulatory subunit 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:33146]","synonyms":"smk1,SMEK3P,FLJ32867,FLFL3P","biotype":"protein_coding","ncbi_id":"139420","summary":null,"start":27460211,"end":27463341,"strand":-1,"description":"protein phosphatase 4 regulatory subunit 3C, pseudogene [Source:HGNC Symbol;Acc:HGNC:33146]"}, {"versioned_ensembl_gene_id":"ENSG00000228691.6","gene_symbol":"NEU1","gene_name":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]","synonyms":"NEU","biotype":"protein_coding","ncbi_id":"4758","summary":"The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]","start":31924682,"end":31929929,"strand":-1,"description":"neuraminidase 1 [Source:HGNC Symbol;Acc:HGNC:7758]"}, {"versioned_ensembl_gene_id":"ENSG00000133884.9","gene_symbol":"DPF2","gene_name":"double PHD fingers 2 [Source:HGNC Symbol;Acc:HGNC:9964]","synonyms":"ubi-d4,REQ,BAF45d","biotype":"protein_coding","ncbi_id":"5977","summary":"The protein encoded by this gene is a member of the d4 domain family, characterized by a zinc finger-like structural motif. This protein functions as a transcription factor which is necessary for the apoptotic response following deprivation of survival factors. It likely serves a regulatory role in rapid hematopoietic cell growth and turnover. This gene is considered a candidate gene for multiple endocrine neoplasia type I, an inherited cancer syndrome involving multiple parathyroid, enteropancreatic, and pituitary tumors. [provided by RefSeq, Jul 2008]","start":65333754,"end":65353249,"strand":1,"description":"double PHD fingers 2 [Source:HGNC Symbol;Acc:HGNC:9964]"}, {"versioned_ensembl_gene_id":"ENSG00000261673.1","gene_symbol":"AC009075.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72224565,"end":72225144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262536.1","gene_symbol":"AC192820.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38949113,"end":38949127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162426.14","gene_symbol":"SLC45A1","gene_name":"solute carrier family 45 member 1 [Source:HGNC Symbol;Acc:HGNC:17939]","synonyms":"DNB5","biotype":"protein_coding","ncbi_id":"50651","summary":"This gene was isolated initially from a region on chromosome 1p that is frequently deleted in human neuroblastoma, although no causal relationship has since been demonstrated. The encoded protein belongs to the glycoside-pentoside-hexuronide cation symporter transporter family and may play a role in glucose uptake. [provided by RefSeq, Mar 2014]","start":8317826,"end":8344167,"strand":1,"description":"solute carrier family 45 member 1 [Source:HGNC Symbol;Acc:HGNC:17939]"}, {"versioned_ensembl_gene_id":"ENSG00000175806.14","gene_symbol":"MSRA","gene_name":"methionine sulfoxide reductase A [Source:HGNC Symbol;Acc:HGNC:7377]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4482","summary":"This gene encodes a ubiquitous and highly conserved protein that carries out the enzymatic reduction of methionine sulfoxide to methionine. Human and animal studies have shown the highest levels of expression in kidney and nervous tissue. The protein functions in the repair of oxidatively damaged proteins to restore biological activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]","start":10054268,"end":10428891,"strand":1,"description":"methionine sulfoxide reductase A [Source:HGNC Symbol;Acc:HGNC:7377]"}, {"versioned_ensembl_gene_id":"ENSG00000139304.12","gene_symbol":"PTPRQ","gene_name":"protein tyrosine phosphatase, receptor type Q [Source:HGNC Symbol;Acc:HGNC:9679]","synonyms":"DFNB84","biotype":"protein_coding","ncbi_id":"374462","summary":"This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]","start":80402178,"end":80680234,"strand":1,"description":"protein tyrosine phosphatase, receptor type Q [Source:HGNC Symbol;Acc:HGNC:9679]"}, {"versioned_ensembl_gene_id":"ENSG00000229923.2","gene_symbol":"AL583803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":130697312,"end":130697778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282006.1","gene_symbol":"AC243660.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28459418,"end":28459575,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233807.1","gene_symbol":"AC097262.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27218131,"end":27218678,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162642.13","gene_symbol":"C1orf52","gene_name":"chromosome 1 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:24871]","synonyms":"gm117,FLJ44982","biotype":"protein_coding","ncbi_id":"148423","summary":null,"start":85249953,"end":85259672,"strand":-1,"description":"chromosome 1 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:24871]"}, {"versioned_ensembl_gene_id":"ENSG00000233492.1","gene_symbol":"AL133325.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21530202,"end":21530744,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257763.1","gene_symbol":"OR5BK1P","gene_name":"olfactory receptor family 5 subfamily BK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14817]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401718","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":48355792,"end":48356614,"strand":-1,"description":"olfactory receptor family 5 subfamily BK member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14817]"}, {"versioned_ensembl_gene_id":"ENSG00000261570.1","gene_symbol":"AC073878.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":141529203,"end":141551304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270157.1","gene_symbol":"AC004918.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":141662922,"end":141663846,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184454.6","gene_symbol":"NCMAP","gene_name":"non-compact myelin associated protein [Source:HGNC Symbol;Acc:HGNC:29332]","synonyms":"MP11,FLJ42528,C1orf130","biotype":"protein_coding","ncbi_id":"400746","summary":null,"start":24556111,"end":24609328,"strand":1,"description":"non-compact myelin associated protein [Source:HGNC Symbol;Acc:HGNC:29332]"}, {"versioned_ensembl_gene_id":"ENSG00000270433.1","gene_symbol":"AL049829.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23293852,"end":23295798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137440.4","gene_symbol":"FGFBP1","gene_name":"fibroblast growth factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19695]","synonyms":"HBP17,FGFBP","biotype":"protein_coding","ncbi_id":"9982","summary":"This gene encodes a secreted fibroblast growth factor carrier protein. The encoded protein plays a critical role in cell proliferation, differentiation and migration by binding to fibroblast growth factors and potentiating their biological effects on target cells. The encoded protein may also play a role in tumor growth as an angiogenic switch molecule, and expression of this gene has been associated with several types of cancer including pancreatic and colorectal adenocarcinoma. A pseudogene of this gene is also located on the short arm of chromosome 4. [provided by RefSeq, Nov 2011]","start":15935569,"end":15938740,"strand":-1,"description":"fibroblast growth factor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:19695]"}, {"versioned_ensembl_gene_id":"ENSG00000213432.2","gene_symbol":"RPL17P34","gene_name":"ribosomal protein L17 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643863","summary":null,"start":93284004,"end":93284558,"strand":-1,"description":"ribosomal protein L17 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:36756]"}, {"versioned_ensembl_gene_id":"ENSG00000213058.3","gene_symbol":"AL365357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":178411616,"end":178411972,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188984.11","gene_symbol":"AADACL3","gene_name":"arylacetamide deacetylase like 3 [Source:HGNC Symbol;Acc:HGNC:32037]","synonyms":"OTTHUMG00000001887","biotype":"protein_coding","ncbi_id":"126767","summary":null,"start":12716115,"end":12728759,"strand":1,"description":"arylacetamide deacetylase like 3 [Source:HGNC Symbol;Acc:HGNC:32037]"}, {"versioned_ensembl_gene_id":"ENSG00000273015.2","gene_symbol":"AC008124.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45718046,"end":45727775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271408.1","gene_symbol":"NAPGP1","gene_name":"N-ethylmaleimide-sensitive factor attachment protein, gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288843","summary":null,"start":88699683,"end":88700401,"strand":1,"description":"N-ethylmaleimide-sensitive factor attachment protein, gamma pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45165]"}, {"versioned_ensembl_gene_id":"ENSG00000273091.1","gene_symbol":"AP000255.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31735732,"end":31736407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282146.1","gene_symbol":"AF186192.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144739024,"end":144760993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229468.1","gene_symbol":"AC097635.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20012452,"end":20012606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276041.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54794554,"end":54798517,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000232648.3","gene_symbol":"AC107214.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":183494938,"end":183504494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276759.2","gene_symbol":"AL353753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26066675,"end":26118408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255267.3","gene_symbol":"AC018716.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45371397,"end":45388508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129636.12","gene_symbol":"ITFG1","gene_name":"integrin alpha FG-GAP repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:30697]","synonyms":"TIP,LNKN-1,CDA08","biotype":"protein_coding","ncbi_id":"81533","summary":null,"start":47154387,"end":47464149,"strand":-1,"description":"integrin alpha FG-GAP repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:30697]"}, {"versioned_ensembl_gene_id":"ENSG00000272677.1","gene_symbol":"AC124016.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82374301,"end":82384027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275228.1","gene_symbol":"AC024257.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48327942,"end":48328472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282914.1","gene_symbol":"Z83818.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87707579,"end":87750883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271205.1","gene_symbol":"Z83818.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":87723089,"end":87723238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064489.22","gene_symbol":"BORCS8-MEF2B","gene_name":"BORCS8-MEF2B readthrough [Source:HGNC Symbol;Acc:HGNC:39979]","synonyms":"MEF2BNB-MEF2B","biotype":"protein_coding","ncbi_id":"4207","summary":"This gene represents numerous read-through transcripts that span GeneID:729991 and 100271849. Many read-through transcripts are predicted to be nonsense-mediated decay (NMD) candidates, and are thought to be non-coding. Some transcripts are predicted to be capable of translation reinitiation at a downstream AUG, resulting in expression of at least one isoform of myocyte enhancer factor 2B (MEF2B) from this read-through locus. At least one additional MEF2B variant and isoform can be expressed from a downstream promoter, and is annotated on GeneID:100271849. [provided by RefSeq, Oct 2010]","start":19145567,"end":19192158,"strand":-1,"description":"BORCS8-MEF2B readthrough [Source:HGNC Symbol;Acc:HGNC:39979]"}, {"versioned_ensembl_gene_id":"ENSG00000264937.1","gene_symbol":"AC100830.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64696622,"end":64696861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181656.6","gene_symbol":"GPR88","gene_name":"G protein-coupled receptor 88 [Source:HGNC Symbol;Acc:HGNC:4539]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54112","summary":"The protein encoded by this gene is a G protein-coupled receptor found almost exclusively in the striatum, a brain structure that controls motor function and cognition. Defects in this gene have been associated with chorea, speech delay, and learning difficulties, as well as some neuropsychiatric disorders. [provided by RefSeq, Mar 2017]","start":100538137,"end":100542018,"strand":1,"description":"G protein-coupled receptor 88 [Source:HGNC Symbol;Acc:HGNC:4539]"}, {"versioned_ensembl_gene_id":"ENSG00000176774.5","gene_symbol":"MAGEB18","gene_name":"MAGE family member B18 [Source:HGNC Symbol;Acc:HGNC:28515]","synonyms":"MGC33889","biotype":"protein_coding","ncbi_id":"286514","summary":null,"start":26138343,"end":26140735,"strand":1,"description":"MAGE family member B18 [Source:HGNC Symbol;Acc:HGNC:28515]"}, {"versioned_ensembl_gene_id":"ENSG00000214668.4","gene_symbol":"SLC29A4P1","gene_name":"solute carrier family 29 member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43783]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"402509","summary":null,"start":57014285,"end":57020273,"strand":-1,"description":"solute carrier family 29 member 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43783]"}, {"versioned_ensembl_gene_id":"ENSG00000227312.2","gene_symbol":"AL445686.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24563627,"end":24563974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087253.12","gene_symbol":"LPCAT2","gene_name":"lysophosphatidylcholine acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:26032]","synonyms":"LysoPAFAT,FLJ20481,AYTL1,AGPAT11","biotype":"protein_coding","ncbi_id":"54947","summary":"This gene encodes a member of the lysophospholipid acyltransferase family. The encoded enzyme may function in two ways: to catalyze the biosynthesis of platelet-activating factor (1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine) from 1-O-alkyl-sn-glycero-3-phosphocholine, and to catalyze the synthesis of glycerophospholipid precursors from arachidonyl-CoA and lysophosphatidylcholine. The encoded protein may function in membrane biogenesis and production of platelet-activating factor in inflammatory cells. The enzyme may localize to the endoplasmic reticulum and the Golgi. [provided by RefSeq, Feb 2009]","start":55508998,"end":55586670,"strand":1,"description":"lysophosphatidylcholine acyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:26032]"}, {"versioned_ensembl_gene_id":"ENSG00000260784.1","gene_symbol":"AC026150.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30516079,"end":30517867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282076.1","gene_symbol":"KCNQ1","gene_name":"potassium voltage-gated channel subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:6294]","synonyms":"KCNA9,KCNA8,LQT1,JLNS1,LQT,KVLQT1,Kv7.1","biotype":"protein_coding","ncbi_id":"3784","summary":"This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]","start":2768844,"end":2849088,"strand":1,"description":"potassium voltage-gated channel subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:6294]"}, {"versioned_ensembl_gene_id":"ENSG00000196922.10","gene_symbol":"ZNF252P","gene_name":"zinc finger protein 252, pseudogene [Source:HGNC Symbol;Acc:HGNC:13046]","synonyms":"ZNF252","biotype":"transcribed_unitary_pseudogene","ncbi_id":"286101","summary":null,"start":144973589,"end":145002895,"strand":-1,"description":"zinc finger protein 252, pseudogene [Source:HGNC Symbol;Acc:HGNC:13046]"}, {"versioned_ensembl_gene_id":"ENSG00000219712.1","gene_symbol":"AL357054.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":669081,"end":670307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214954.8","gene_symbol":"LRRC69","gene_name":"leucine rich repeat containing 69 [Source:HGNC Symbol;Acc:HGNC:34303]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130742","summary":null,"start":91101832,"end":91219236,"strand":1,"description":"leucine rich repeat containing 69 [Source:HGNC Symbol;Acc:HGNC:34303]"}, {"versioned_ensembl_gene_id":"ENSG00000172493.20","gene_symbol":"AFF1","gene_name":"AF4/FMR2 family member 1 [Source:HGNC Symbol;Acc:HGNC:7135]","synonyms":"PBM1,MLLT2,AF4,AF-4","biotype":"protein_coding","ncbi_id":"4299","summary":"This gene encodes a member of the AF4/ lymphoid nuclear protein related to the Fragile X E syndrome (FRAXE) family of proteins, which have been implicated in human childhood lymphoblastic leukemia, fragile chromosome X intellectual disability, and ataxia. It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia. Members of this family have three conserved domains: an N-terminal homology domain, an AF4/ lymphoid nuclear protein domain, and a C-terminal homology domain. The protein functions as a regulator of RNA polymerase II-mediated transcription through elongation and chromatin remodeling functions. Through RNA interference screens, this gene has been shown to promote the expression of CD133, a plasma membrane glycoprotein required for leukemia cell survival. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":86935002,"end":87141054,"strand":1,"description":"AF4/FMR2 family member 1 [Source:HGNC Symbol;Acc:HGNC:7135]"}, {"versioned_ensembl_gene_id":"ENSG00000259246.4","gene_symbol":"HMGN2P47","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:44422]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480791","summary":null,"start":67000814,"end":67001085,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:44422]"}, {"versioned_ensembl_gene_id":"ENSG00000130701.3","gene_symbol":"RBBP8NL","gene_name":"RBBP8 N-terminal like [Source:HGNC Symbol;Acc:HGNC:16144]","synonyms":"dJ908M14.3,C20orf151","biotype":"protein_coding","ncbi_id":"140893","summary":null,"start":62410237,"end":62427533,"strand":-1,"description":"RBBP8 N-terminal like [Source:HGNC Symbol;Acc:HGNC:16144]"}, {"versioned_ensembl_gene_id":"ENSG00000216490.3","gene_symbol":"IFI30","gene_name":"IFI30, lysosomal thiol reductase [Source:HGNC Symbol;Acc:HGNC:5398]","synonyms":"IP30,IP-30,IFI-30,GILT,MGC32056","biotype":"protein_coding","ncbi_id":"10437","summary":"The protein encoded by this gene is a lysosomal thiol reductase that at low pH can reduce protein disulfide bonds. The enzyme is expressed constitutively in antigen-presenting cells and induced by gamma-interferon in other cell types. This enzyme has an important role in MHC class II-restricted antigen processing. [provided by RefSeq, Jul 2008]","start":18173162,"end":18178117,"strand":1,"description":"IFI30, lysosomal thiol reductase [Source:HGNC Symbol;Acc:HGNC:5398]"}, {"versioned_ensembl_gene_id":"ENSG00000275118.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173853,"end":54190413,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000231403.1","gene_symbol":"AC099344.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11388023,"end":11390367,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225876.1","gene_symbol":"AC024067.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":26244351,"end":26244573,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185736.15","gene_symbol":"ADARB2","gene_name":"adenosine deaminase, RNA specific B2 (inactive) [Source:HGNC Symbol;Acc:HGNC:227]","synonyms":"RED2,hRED2,ADAR3","biotype":"protein_coding","ncbi_id":"105","summary":"This gene encodes a member of the double-stranded RNA adenosine deaminase family of RNA-editing enzymes and may play a regulatory role in RNA editing. [provided by RefSeq, Jul 2008]","start":1177318,"end":1737476,"strand":-1,"description":"adenosine deaminase, RNA specific B2 (inactive) [Source:HGNC Symbol;Acc:HGNC:227]"}, {"versioned_ensembl_gene_id":"ENSG00000112685.13","gene_symbol":"EXOC2","gene_name":"exocyst complex component 2 [Source:HGNC Symbol;Acc:HGNC:24968]","synonyms":"Sec5p,SEC5L1,FLJ11026","biotype":"protein_coding","ncbi_id":"55770","summary":"The protein encoded by this gene is a component of the exocyst complex, a multi-protein complex essential for the polarized targeting of exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and the functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. This interaction has been shown to mediate filopodia formation in fibroblasts. This protein has been shown to interact with the Ral subfamily of GTPases and thereby mediate exocytosis by tethering vesicles to the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":485133,"end":693111,"strand":-1,"description":"exocyst complex component 2 [Source:HGNC Symbol;Acc:HGNC:24968]"}, {"versioned_ensembl_gene_id":"ENSG00000259665.1","gene_symbol":"AC021231.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35081144,"end":35081513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259181.1","gene_symbol":"AC114546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34993646,"end":35003221,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129873.7","gene_symbol":"CDY2B","gene_name":"chromodomain Y-linked 2B [Source:HGNC Symbol;Acc:HGNC:23921]","synonyms":"CDY","biotype":"protein_coding","ncbi_id":"203611","summary":"This intronless gene encodes a protein containing a chromodomain and a histone acetyltransferase catalytic domain. Chromodomain proteins are components of heterochromatin-like complexes and can act as gene repressors. This protein is localized to the nucleus of late spermatids where histone hyperacetylation takes place. Histone hyperacetylation is thought to facilitate the transition in which protamines replace histones as the major DNA-packaging protein. Two nearly identical copies of this gene are found in a palindromic region on chromosome Y; this record represents the centromeric copy. Chromosome Y also contains a pair of closely related genes in another more telomeric palindrome as well as several related pseudogenes. [provided by RefSeq, Jul 2008]","start":17877410,"end":17880220,"strand":-1,"description":"chromodomain Y-linked 2B [Source:HGNC Symbol;Acc:HGNC:23921]"}, {"versioned_ensembl_gene_id":"ENSG00000269509.1","gene_symbol":"BNIP3P34","gene_name":"BCL2 interacting protein 3 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:49714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128849","summary":null,"start":22773853,"end":22774424,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:49714]"}, {"versioned_ensembl_gene_id":"ENSG00000182333.14","gene_symbol":"LIPF","gene_name":"lipase F, gastric type [Source:HGNC Symbol;Acc:HGNC:6622]","synonyms":"HLAL,HGL","biotype":"protein_coding","ncbi_id":"8513","summary":"This gene encodes gastric lipase, an enzyme involved in the digestion of dietary triglycerides in the gastrointestinal tract, and responsible for 30% of fat digestion processes occurring in human. It is secreted by gastric chief cells in the fundic mucosa of the stomach, and it hydrolyzes the ester bonds of triglycerides under acidic pH conditions. The gene is a member of a conserved gene family of lipases that play distinct roles in neutral lipid metabolism. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":88664441,"end":88678814,"strand":1,"description":"lipase F, gastric type [Source:HGNC Symbol;Acc:HGNC:6622]"}, {"versioned_ensembl_gene_id":"ENSG00000105135.15","gene_symbol":"ILVBL","gene_name":"ilvB acetolactate synthase like [Source:HGNC Symbol;Acc:HGNC:6041]","synonyms":"MGC19535,MGC1269,ILV2H,HACL1L,FLJ39061,AHAS,209L8","biotype":"protein_coding","ncbi_id":"10994","summary":"The protein encoded by this gene shares similarity with several thiamine pyrophosphate-binding proteins identified in bacteria, yeast, and plants. The highest degree of similarity is found with bacterial acetolactate synthases (AHAS), which are enzymes that catalyze the first step in branched-chain amino acid biosynthesis. [provided by RefSeq, Jul 2008]","start":15114984,"end":15125785,"strand":-1,"description":"ilvB acetolactate synthase like [Source:HGNC Symbol;Acc:HGNC:6041]"}, {"versioned_ensembl_gene_id":"ENSG00000268564.1","gene_symbol":"AC003956.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15124160,"end":15126174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266268.5","gene_symbol":"AP005203.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4775054,"end":5004537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183690.12","gene_symbol":"EFHC2","gene_name":"EF-hand domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26233]","synonyms":"MRX74,FLJ22843","biotype":"protein_coding","ncbi_id":"80258","summary":"This gene encodes a protein which contains three DM10 domains and three calcium-binding EF-hand motifs. A related protein is encoded by a gene on chromosome 6. It has been suggested that both proteins are involved in the development of epilepsy (PMID: 15258581, 16112844) and that this gene may be associated with fear recognition in individuals with Turner syndrome. [provided by RefSeq, Aug 2011]","start":44147882,"end":44343672,"strand":-1,"description":"EF-hand domain containing 2 [Source:HGNC Symbol;Acc:HGNC:26233]"}, {"versioned_ensembl_gene_id":"ENSG00000175886.10","gene_symbol":"RPL7AP66","gene_name":"ribosomal protein L7a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35682]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"388474","summary":null,"start":39334872,"end":39335672,"strand":-1,"description":"ribosomal protein L7a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35682]"}, {"versioned_ensembl_gene_id":"ENSG00000236790.5","gene_symbol":"LINC00299","gene_name":"long intergenic non-protein coding RNA 299 [Source:HGNC Symbol;Acc:HGNC:27940]","synonyms":"NCRNA00299,FLJ45673,C2orf46","biotype":"lincRNA","ncbi_id":"339789","summary":null,"start":8007771,"end":8383621,"strand":-1,"description":"long intergenic non-protein coding RNA 299 [Source:HGNC Symbol;Acc:HGNC:27940]"}, {"versioned_ensembl_gene_id":"ENSG00000242608.1","gene_symbol":"RPS23P5","gene_name":"ribosomal protein S23 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35726]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271093","summary":null,"start":13250235,"end":13250662,"strand":-1,"description":"ribosomal protein S23 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35726]"}, {"versioned_ensembl_gene_id":"ENSG00000186648.14","gene_symbol":"CARMIL3","gene_name":"capping protein regulator and myosin 1 linker 3 [Source:HGNC Symbol;Acc:HGNC:20272]","synonyms":"LRRC16B,crml-1,C14orf121,BC008134","biotype":"protein_coding","ncbi_id":"90668","summary":null,"start":24052000,"end":24069728,"strand":1,"description":"capping protein regulator and myosin 1 linker 3 [Source:HGNC Symbol;Acc:HGNC:20272]"}, {"versioned_ensembl_gene_id":"ENSG00000250868.4","gene_symbol":"XKRY","gene_name":"XK related, Y-linked [Source:HGNC Symbol;Acc:HGNC:18571]","synonyms":"XKRY1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"9082","summary":"This probable pseudogene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It is similar to the XK (X-linked Kell blood group precursor) gene, which encodes a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more centromeric copy. [provided by RefSeq, Nov 2020]","start":17768980,"end":17777400,"strand":-1,"description":"XK related, Y-linked [Source:HGNC Symbol;Acc:HGNC:18571]"}, {"versioned_ensembl_gene_id":"ENSG00000271611.1","gene_symbol":"AC006006.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140934867,"end":140935010,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278758.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54864015,"end":54880809,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000250826.2","gene_symbol":"HNRNPA3P13","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441026","summary":null,"start":82128535,"end":82129656,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48759]"}, {"versioned_ensembl_gene_id":"ENSG00000273184.1","gene_symbol":"AC010655.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":128455840,"end":128493859,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166716.9","gene_symbol":"ZNF592","gene_name":"zinc finger protein 592 [Source:HGNC Symbol;Acc:HGNC:28986]","synonyms":"SCAR5,KIAA0211,CAMOS","biotype":"protein_coding","ncbi_id":"9640","summary":"This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]","start":84748635,"end":84806432,"strand":1,"description":"zinc finger protein 592 [Source:HGNC Symbol;Acc:HGNC:28986]"}, {"versioned_ensembl_gene_id":"ENSG00000283403.1","gene_symbol":"AC005394.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28435388,"end":28727680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226098.4","gene_symbol":"SEC11B","gene_name":"SEC11 homolog B, signal peptidase complex subunit (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31884]","synonyms":"SPCS4B,SEC11L2","biotype":"processed_pseudogene","ncbi_id":"157708","summary":null,"start":54522799,"end":54523297,"strand":-1,"description":"SEC11 homolog B, signal peptidase complex subunit (pseudogene) [Source:HGNC Symbol;Acc:HGNC:31884]"}, {"versioned_ensembl_gene_id":"ENSG00000226878.2","gene_symbol":"GSTM3P2","gene_name":"glutathione S-transferase mu 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38006]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421057","summary":null,"start":159056005,"end":159056859,"strand":-1,"description":"glutathione S-transferase mu 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38006]"}, {"versioned_ensembl_gene_id":"ENSG00000234968.1","gene_symbol":"HLA-DQB3","gene_name":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]","synonyms":"D6S205,DQB3,HLA-DVB,D6S205E,DVB","biotype":"unprocessed_pseudogene","ncbi_id":"3121","summary":null,"start":32822370,"end":32823307,"strand":-1,"description":"major histocompatibility complex, class II, DQ beta 3 [Source:HGNC Symbol;Acc:HGNC:4946]"}, {"versioned_ensembl_gene_id":"ENSG00000282155.1","gene_symbol":"AC093627.13","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77038,"end":80418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280765.1","gene_symbol":"AL121956.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166236969,"end":166256947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280557.1","gene_symbol":"GNG5P1","gene_name":"G protein subunit gamma 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4409]","synonyms":"GNG5P","biotype":"processed_pseudogene","ncbi_id":"2789","summary":null,"start":166240290,"end":166240493,"strand":-1,"description":"G protein subunit gamma 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4409]"}, {"versioned_ensembl_gene_id":"ENSG00000113594.9","gene_symbol":"LIFR","gene_name":"LIF receptor alpha [Source:HGNC Symbol;Acc:HGNC:6597]","synonyms":"CD118","biotype":"protein_coding","ncbi_id":"3977","summary":"This gene encodes a protein that belongs to the type I cytokine receptor family. This protein combines with a high-affinity converter subunit, gp130, to form a receptor complex that mediates the action of the leukemia inhibitory factor, a polyfunctional cytokine that is involved in cellular differentiation, proliferation and survival in the adult and the embryo. Mutations in this gene cause Schwartz-Jampel syndrome type 2, a disease belonging to the group of the bent-bone dysplasias. A translocation that involves the promoter of this gene, t(5;8)(p13;q12) with the pleiomorphic adenoma gene 1, is associated with salivary gland pleiomorphic adenoma, a common type of benign epithelial tumor of the salivary gland. Multiple splice variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2018]","start":38474963,"end":38608354,"strand":-1,"description":"LIF receptor alpha [Source:HGNC Symbol;Acc:HGNC:6597]"}, {"versioned_ensembl_gene_id":"ENSG00000244968.6","gene_symbol":"LIFR-AS1","gene_name":"LIFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43600]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506495","summary":null,"start":38556786,"end":38671216,"strand":1,"description":"LIFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43600]"}, {"versioned_ensembl_gene_id":"ENSG00000253872.1","gene_symbol":"AC083836.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":95505406,"end":95527524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253351.1","gene_symbol":"LINC01298","gene_name":"long intergenic non-protein coding RNA 1298 [Source:HGNC Symbol;Acc:HGNC:32292]","synonyms":"C8orf69","biotype":"lincRNA","ncbi_id":"619344","summary":null,"start":95207007,"end":95216374,"strand":-1,"description":"long intergenic non-protein coding RNA 1298 [Source:HGNC Symbol;Acc:HGNC:32292]"}, {"versioned_ensembl_gene_id":"ENSG00000142449.12","gene_symbol":"FBN3","gene_name":"fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84467","summary":"This gene encodes a memebr of the fibrillin protein family. Fibrillins are extracellular matrix molecules that assemble into microfibrils in many connective tissues. This gene is most highly expressed in fetal tissues and its protein product is localized to extracellular microfibrils of developing skeletal elements, skin, lung, kidney, and skeletal muscle. This gene is potentially involved in Weill-Marchesani syndrome. [provided by RefSeq, Mar 2016]","start":8065402,"end":8149846,"strand":-1,"description":"fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]"}, {"versioned_ensembl_gene_id":"ENSG00000253945.1","gene_symbol":"AC024995.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95403802,"end":95403894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196329.11","gene_symbol":"GIMAP5","gene_name":"GTPase, IMAP family member 5 [Source:HGNC Symbol;Acc:HGNC:18005]","synonyms":"IAN5,IAN4L1,HIMAP3","biotype":"protein_coding","ncbi_id":"55340","summary":"This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. This gene encodes an antiapoptotic protein that functions in T-cell survival. Polymorphisms in this gene are associated with systemic lupus erythematosus. Read-through transcription exists between this gene and the neighboring upstream GIMAP1 (GTPase, IMAP family member 1) gene. [provided by RefSeq, Dec 2010]","start":150722253,"end":150750033,"strand":1,"description":"GTPase, IMAP family member 5 [Source:HGNC Symbol;Acc:HGNC:18005]"}, {"versioned_ensembl_gene_id":"ENSG00000278890.1","gene_symbol":"FP325330.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48052646,"end":48058275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166451.13","gene_symbol":"CENPN","gene_name":"centromere protein N [Source:HGNC Symbol;Acc:HGNC:30873]","synonyms":"FLJ22660,FLJ13607,C16orf60,BM039","biotype":"protein_coding","ncbi_id":"55839","summary":"The protein encoded by this gene forms part of the nucleosome-associated complex and is important for kinetochore assembly. It is bound to kinetochores during S phase and G2 and recruits other proteins to the centromere. Pseudogenes of this gene are located on chromosome 2. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":81006498,"end":81033114,"strand":1,"description":"centromere protein N [Source:HGNC Symbol;Acc:HGNC:30873]"}, {"versioned_ensembl_gene_id":"ENSG00000085433.15","gene_symbol":"WDR47","gene_name":"WD repeat domain 47 [Source:HGNC Symbol;Acc:HGNC:29141]","synonyms":"KIAA0893","biotype":"protein_coding","ncbi_id":"22911","summary":null,"start":108970214,"end":109042113,"strand":-1,"description":"WD repeat domain 47 [Source:HGNC Symbol;Acc:HGNC:29141]"}, {"versioned_ensembl_gene_id":"ENSG00000237349.1","gene_symbol":"BX679664.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108986963,"end":108987245,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188089.13","gene_symbol":"PLA2G4E","gene_name":"phospholipase A2 group IVE [Source:HGNC Symbol;Acc:HGNC:24791]","synonyms":"FLJ45651","biotype":"protein_coding","ncbi_id":"123745","summary":"This gene encodes a member of the cytosolic phospholipase A2 group IV family. Members of this family are involved in regulation of membrane tubule-mediated transport. The enzyme encoded by this member of the family plays a role in trafficking through the clathrin-independent endocytic pathway. The enzyme regulates the recycling process via formation of tubules that transport internalized clathrin-independent cargo proteins back to the cell surface. [provided by RefSeq, Jan 2017]","start":41981582,"end":42051190,"strand":-1,"description":"phospholipase A2 group IVE [Source:HGNC Symbol;Acc:HGNC:24791]"}, {"versioned_ensembl_gene_id":"ENSG00000126067.11","gene_symbol":"PSMB2","gene_name":"proteasome subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:9539]","synonyms":"HC7-I","biotype":"protein_coding","ncbi_id":"5690","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":35599544,"end":35641844,"strand":-1,"description":"proteasome subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:9539]"}, {"versioned_ensembl_gene_id":"ENSG00000205559.3","gene_symbol":"CHKB-AS1","gene_name":"CHKB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40146]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100144603","summary":null,"start":50583026,"end":50583877,"strand":1,"description":"CHKB antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:40146]"}, {"versioned_ensembl_gene_id":"ENSG00000273821.1","gene_symbol":"AL096828.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63218041,"end":63218502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213626.11","gene_symbol":"LBH","gene_name":"limb bud and heart development [Source:HGNC Symbol;Acc:HGNC:29532]","synonyms":null,"biotype":"protein_coding","ncbi_id":"81606","summary":null,"start":30231531,"end":30323730,"strand":1,"description":"limb bud and heart development [Source:HGNC Symbol;Acc:HGNC:29532]"}, {"versioned_ensembl_gene_id":"ENSG00000248282.1","gene_symbol":"MTCYBP44","gene_name":"mitochondrially encoded cytochrome b pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52312]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729154","summary":null,"start":81733385,"end":81734207,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:52312]"}, {"versioned_ensembl_gene_id":"ENSG00000260693.1","gene_symbol":"AC026150.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30540093,"end":30545969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000008710.19","gene_symbol":"PKD1","gene_name":"polycystin 1, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:9008]","synonyms":"TRPP1,Pc-1,PBP","biotype":"protein_coding","ncbi_id":"5310","summary":"This gene encodes a member of the polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described. [provided by RefSeq, Oct 2008]","start":2088710,"end":2135898,"strand":-1,"description":"polycystin 1, transient receptor potential channel interacting [Source:HGNC Symbol;Acc:HGNC:9008]"}, {"versioned_ensembl_gene_id":"ENSG00000100060.17","gene_symbol":"MFNG","gene_name":"MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7038]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4242","summary":"This gene is a member of the glycosyltransferase 31 gene family. Members of this gene family, which also includes the LFNG (GeneID: 3955) and RFNG (GeneID: 5986) genes, encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, these proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling. The protein encoded by this gene may control Notch signaling in claudin-low breast cancer. [provided by RefSeq, May 2018]","start":37469063,"end":37486401,"strand":-1,"description":"MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:7038]"}, {"versioned_ensembl_gene_id":"ENSG00000284380.1","gene_symbol":"AC006328.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":25464006,"end":25473621,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247473.2","gene_symbol":"CARS-AS1","gene_name":"CARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40125]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100852407","summary":null,"start":3029009,"end":3041260,"strand":1,"description":"CARS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40125]"}, {"versioned_ensembl_gene_id":"ENSG00000158552.12","gene_symbol":"ZFAND2B","gene_name":"zinc finger AN1-type containing 2B [Source:HGNC Symbol;Acc:HGNC:25206]","synonyms":"AIRAPL","biotype":"protein_coding","ncbi_id":"130617","summary":"This gene encodes a protein containing AN1-type zinc-fingers and ubiquitin-interacting motifs. The encoded protein likely associates with the proteosome to stimulate the degradation of toxic or misfolded proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":219195237,"end":219209651,"strand":1,"description":"zinc finger AN1-type containing 2B [Source:HGNC Symbol;Acc:HGNC:25206]"}, {"versioned_ensembl_gene_id":"ENSG00000242195.1","gene_symbol":"SRRM1P2","gene_name":"serine/arginine repetitive matrix 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38163]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420834","summary":null,"start":83937045,"end":83938236,"strand":1,"description":"serine/arginine repetitive matrix 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38163]"}, {"versioned_ensembl_gene_id":"ENSG00000115109.13","gene_symbol":"EPB41L5","gene_name":"erythrocyte membrane protein band 4.1 like 5 [Source:HGNC Symbol;Acc:HGNC:19819]","synonyms":"FLJ12957,BE37,YRT,YMO1,KIAA1548","biotype":"protein_coding","ncbi_id":"57669","summary":null,"start":120013005,"end":120179119,"strand":1,"description":"erythrocyte membrane protein band 4.1 like 5 [Source:HGNC Symbol;Acc:HGNC:19819]"}, {"versioned_ensembl_gene_id":"ENSG00000153898.12","gene_symbol":"MCOLN2","gene_name":"mucolipin 2 [Source:HGNC Symbol;Acc:HGNC:13357]","synonyms":"TRPML2,TRP-ML2,FLJ36691","biotype":"protein_coding","ncbi_id":"255231","summary":"Mucolipins constitute a family of cation channel proteins with homology to the transient receptor potential superfamily. In mammals, the mucolipin family includes 3 members, MCOLN1 (MIM 605248), MCOLN2, and MCOLN3 (MIM 607400), that exhibit a common 6-membrane-spanning topology. Homologs of mammalian mucolipins exist in Drosophila and C. elegans. Mutations in the human MCOLN1 gene cause mucolipodosis IV (MIM 262650) (Karacsonyi et al., 2007 [PubMed 17662026]).[supplied by OMIM, Sep 2009]","start":84925583,"end":84997113,"strand":-1,"description":"mucolipin 2 [Source:HGNC Symbol;Acc:HGNC:13357]"}, {"versioned_ensembl_gene_id":"ENSG00000279550.1","gene_symbol":"AL359757.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25190063,"end":25190317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224789.1","gene_symbol":"AC012363.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120174885,"end":120216544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179934.6","gene_symbol":"CCR8","gene_name":"C-C motif chemokine receptor 8 [Source:HGNC Symbol;Acc:HGNC:1609]","synonyms":"TER1,GPR-CY6,CY6,CMKBRL2,CMKBR8,CKR-L1,CDw198","biotype":"protein_coding","ncbi_id":"1237","summary":"This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. Chemokines and their receptors are important for the migration of various cell types into the inflammatory sites. This receptor protein preferentially expresses in the thymus. I-309, thymus activation-regulated cytokine (TARC) and macrophage inflammatory protein-1 beta (MIP-1 beta) have been identified as ligands of this receptor. Studies of this receptor and its ligands suggested its role in regulation of monocyte chemotaxis and thymic cell apoptosis. More specifically, this receptor may contribute to the proper positioning of activated T cells within the antigenic challenge sites and specialized areas of lymphoid tissues. This gene is located at the chemokine receptor gene cluster region. [provided by RefSeq, Jul 2008]","start":39329706,"end":39333511,"strand":1,"description":"C-C motif chemokine receptor 8 [Source:HGNC Symbol;Acc:HGNC:1609]"}, {"versioned_ensembl_gene_id":"ENSG00000152669.8","gene_symbol":"CCNO","gene_name":"cyclin O [Source:HGNC Symbol;Acc:HGNC:18576]","synonyms":"FLJ22422,CCNU,UNG2,UDG2","biotype":"protein_coding","ncbi_id":"10309","summary":"This gene encodes a member of the cyclin protein family, and the encoded protein is involved in regulation of the cell cycle. Disruption of this gene is associated with primary ciliary dyskinesia-19. Alternative splicing results in multiple transcript variants. This gene, which has a previous symbol of UNG2, was erroneously identified as a uracil DNA glycosylase in PubMed ID: 2001396. A later publication, PubMed ID: 8419333, identified this gene's product as a cyclin protein family member. The UNG2 symbol is also used as a specific protein isoform name for the UNG gene (GeneID 7374), so confusion exists in the scientific literature and in some databases for these two genes. [provided by RefSeq, Jul 2014]","start":55231152,"end":55233680,"strand":-1,"description":"cyclin O [Source:HGNC Symbol;Acc:HGNC:18576]"}, {"versioned_ensembl_gene_id":"ENSG00000243296.1","gene_symbol":"AC078828.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":99500347,"end":99505508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260273.1","gene_symbol":"AL359711.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109382795,"end":109383666,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273533.3","gene_symbol":"FAM181A","gene_name":"family with sequence similarity 181 member A [Source:HGNC Symbol;Acc:HGNC:20491]","synonyms":"C14orf152","biotype":"protein_coding","ncbi_id":"90050","summary":null,"start":93918894,"end":93929608,"strand":1,"description":"family with sequence similarity 181 member A [Source:HGNC Symbol;Acc:HGNC:20491]"}, {"versioned_ensembl_gene_id":"ENSG00000224979.6","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"G7b,C6orf28,YBL026W","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31864414,"end":31874003,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000233317.1","gene_symbol":"MTCO3P1","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]","synonyms":"U92032.1","biotype":"unprocessed_pseudogene","ncbi_id":"404026","summary":null,"start":32798219,"end":32799050,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31342]"}, {"versioned_ensembl_gene_id":"ENSG00000249074.1","gene_symbol":"NDUFB2P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52266]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075208","summary":null,"start":154724586,"end":154724880,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52266]"}, {"versioned_ensembl_gene_id":"ENSG00000270367.1","gene_symbol":"AC092053.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39285985,"end":39287920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224207.3","gene_symbol":"AC018797.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":102734358,"end":102734612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242349.5","gene_symbol":"NPPA-AS1","gene_name":"NPPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37635]","synonyms":"NPPAAS,NPPA-AS","biotype":"antisense_RNA","ncbi_id":"100379251","summary":null,"start":11841017,"end":11848079,"strand":1,"description":"NPPA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:37635]"}, {"versioned_ensembl_gene_id":"ENSG00000276986.2","gene_symbol":"HEATR9","gene_name":"HEAT repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:26548]","synonyms":"FLJ32830,C17orf66","biotype":"protein_coding","ncbi_id":"256957","summary":null,"start":35854946,"end":35868891,"strand":-1,"description":"HEAT repeat containing 9 [Source:HGNC Symbol;Acc:HGNC:26548]"}, {"versioned_ensembl_gene_id":"ENSG00000282202.1","gene_symbol":"AC015849.10","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35816717,"end":35830293,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259598.1","gene_symbol":"AC116158.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38524070,"end":38534655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269678.1","gene_symbol":"OR7A18P","gene_name":"olfactory receptor family 7 subfamily A member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:15399]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81081","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":14886839,"end":14887115,"strand":-1,"description":"olfactory receptor family 7 subfamily A member 18 pseudogene [Source:HGNC Symbol;Acc:HGNC:15399]"}, {"versioned_ensembl_gene_id":"ENSG00000120925.15","gene_symbol":"RNF170","gene_name":"ring finger protein 170 [Source:HGNC Symbol;Acc:HGNC:25358]","synonyms":"SNAX1,DKFZP564A022,ADSA","biotype":"protein_coding","ncbi_id":"81790","summary":"This gene encodes a RING domain-containing protein that resides in the endoplasmic reticulum (ER) membrane. This protein functions as an E3 ubiquitin ligase and mediates ubiquitination and processing of inositol 1,4,5-trisphosphate (IP3) receptors via the ER-associated protein degradation pathway. It is recruited to the activated IP3 receptors by the ERLIN1/ERLIN2 complex to which it is constitutively bound. Mutations in this gene are associated with autosomal dominant sensory ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]","start":42849637,"end":42897290,"strand":-1,"description":"ring finger protein 170 [Source:HGNC Symbol;Acc:HGNC:25358]"}, {"versioned_ensembl_gene_id":"ENSG00000130479.10","gene_symbol":"MAP1S","gene_name":"microtubule associated protein 1S [Source:HGNC Symbol;Acc:HGNC:15715]","synonyms":"VCY2IP1,MAP8,FLJ10669,C19orf5,BPY2IP1","biotype":"protein_coding","ncbi_id":"55201","summary":null,"start":17719242,"end":17734516,"strand":1,"description":"microtubule associated protein 1S [Source:HGNC Symbol;Acc:HGNC:15715]"}, {"versioned_ensembl_gene_id":"ENSG00000255692.1","gene_symbol":"AC002563.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119699768,"end":119701011,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243658.1","gene_symbol":"MTND5P16","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42278]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100862854","summary":null,"start":106898889,"end":106900591,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:42278]"}, {"versioned_ensembl_gene_id":"ENSG00000224791.1","gene_symbol":"KRT18P39","gene_name":"keratin 18 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:33408]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344462","summary":null,"start":203764295,"end":203765593,"strand":-1,"description":"keratin 18 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:33408]"}, {"versioned_ensembl_gene_id":"ENSG00000224836.1","gene_symbol":"AL356498.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1151807,"end":1152140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092067.5","gene_symbol":"CEBPE","gene_name":"CCAAT/enhancer binding protein epsilon [Source:HGNC Symbol;Acc:HGNC:1836]","synonyms":"CRP1","biotype":"protein_coding","ncbi_id":"1053","summary":"The protein encoded by this gene is a bZIP transcription factor which can bind as a homodimer to certain DNA regulatory regions. It can also form heterodimers with the related protein CEBP-delta. The encoded protein may be essential for terminal differentiation and functional maturation of committed granulocyte progenitor cells. Mutations in this gene have been associated with Specific Granule Deficiency, a rare congenital disorder. Multiple variants of this gene have been described, but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]","start":23117304,"end":23119616,"strand":-1,"description":"CCAAT/enhancer binding protein epsilon [Source:HGNC Symbol;Acc:HGNC:1836]"}, {"versioned_ensembl_gene_id":"ENSG00000227268.3","gene_symbol":"KLLN","gene_name":"killin, p53-regulated DNA replication inhibitor [Source:HGNC Symbol;Acc:HGNC:37212]","synonyms":"killin,killin","biotype":"protein_coding","ncbi_id":"100144748","summary":"The protein encoded by this intronless gene is found in the nucleus, where it can inhibit DNA synthesis and promote S phase arrest coupled to apoptosis. The expression of this DNA binding protein is upregulated by transcription factor p53. [provided by RefSeq, Dec 2012]","start":87859161,"end":87863437,"strand":-1,"description":"killin, p53-regulated DNA replication inhibitor [Source:HGNC Symbol;Acc:HGNC:37212]"}, {"versioned_ensembl_gene_id":"ENSG00000151718.15","gene_symbol":"WWC2","gene_name":"WW and C2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24148]","synonyms":"FLJ22029,BOMB","biotype":"protein_coding","ncbi_id":"80014","summary":"This gene encodes a member of the WW-and-C2-domain-containing family of proteins. Members of this family have two N-terminal WW domains that mediate binding to target proteins harboring L/PPxY motifs, an internal C2 domain for membrane association, and C-terminal alpha protein kinase C binding sites and class III PDZ domain-interaction motifs. Proteins of this family are able to form homo- and heterodimers and to modulate hippo pathway signaling. [provided by RefSeq, Sep 2016]","start":183099293,"end":183320777,"strand":1,"description":"WW and C2 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:24148]"}, {"versioned_ensembl_gene_id":"ENSG00000164687.10","gene_symbol":"FABP5","gene_name":"fatty acid binding protein 5 [Source:HGNC Symbol;Acc:HGNC:3560]","synonyms":"PA-FABP,KFABP,E-FABP","biotype":"protein_coding","ncbi_id":"2171","summary":"This gene encodes the fatty acid binding protein found in epidermal cells, and was first identified as being upregulated in psoriasis tissue. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABPs may play roles in fatty acid uptake, transport, and metabolism. Polymorphisms in this gene are associated with type 2 diabetes. The human genome contains many pseudogenes similar to this locus.[provided by RefSeq, Feb 2011]","start":81280363,"end":81284777,"strand":1,"description":"fatty acid binding protein 5 [Source:HGNC Symbol;Acc:HGNC:3560]"}, {"versioned_ensembl_gene_id":"ENSG00000284418.1","gene_symbol":"AL391117.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22703516,"end":23438700,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223906.1","gene_symbol":"AC104457.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100344477,"end":100345242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000013588.7","gene_symbol":"GPRC5A","gene_name":"G protein-coupled receptor class C group 5 member A [Source:HGNC Symbol;Acc:HGNC:9836]","synonyms":"TIG1,RAIG1,RAI3,PEIG-1","biotype":"protein_coding","ncbi_id":"9052","summary":"This gene encodes a member of the type 3 G protein-coupling receptor family, characterized by the signature 7-transmembrane domain motif. The encoded protein may be involved in interaction between retinoid acid and G protein signalling pathways. Retinoic acid plays a critical role in development, cellular growth, and differentiation. This gene may play a role in embryonic development and epithelial cell differentiation. [provided by RefSeq, Jul 2008]","start":12890782,"end":12917937,"strand":1,"description":"G protein-coupled receptor class C group 5 member A [Source:HGNC Symbol;Acc:HGNC:9836]"}, {"versioned_ensembl_gene_id":"ENSG00000239473.1","gene_symbol":"RPL7P38","gene_name":"ribosomal protein L7 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36731]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"120872","summary":null,"start":80028893,"end":80029631,"strand":1,"description":"ribosomal protein L7 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36731]"}, {"versioned_ensembl_gene_id":"ENSG00000263809.1","gene_symbol":"AC135178.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8368638,"end":8383187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121691.4","gene_symbol":"CAT","gene_name":"catalase [Source:HGNC Symbol;Acc:HGNC:1516]","synonyms":null,"biotype":"protein_coding","ncbi_id":"847","summary":"This gene encodes catalase, a key antioxidant enzyme in the bodies defense against oxidative stress. Catalase is a heme enzyme that is present in the peroxisome of nearly all aerobic cells. Catalase converts the reactive oxygen species hydrogen peroxide to water and oxygen and thereby mitigates the toxic effects of hydrogen peroxide. Oxidative stress is hypothesized to play a role in the development of many chronic or late-onset diseases such as diabetes, asthma, Alzheimer's disease, systemic lupus erythematosus, rheumatoid arthritis, and cancers. Polymorphisms in this gene have been associated with decreases in catalase activity but, to date, acatalasemia is the only disease known to be caused by this gene. [provided by RefSeq, Oct 2009]","start":34438925,"end":34472062,"strand":1,"description":"catalase [Source:HGNC Symbol;Acc:HGNC:1516]"}, {"versioned_ensembl_gene_id":"ENSG00000211788.2","gene_symbol":"TRAV13-1","gene_name":"T-cell receptor alpha variable 13-1 [Source:HGNC Symbol;Acc:HGNC:12108]","synonyms":null,"biotype":"TR_V_gene","ncbi_id":"28671","summary":"T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]","start":21868839,"end":21869365,"strand":1,"description":"T-cell receptor alpha variable 13-1 [Source:HGNC Symbol;Acc:HGNC:12108]"}, {"versioned_ensembl_gene_id":"ENSG00000166446.14","gene_symbol":"CDYL2","gene_name":"chromodomain Y like 2 [Source:HGNC Symbol;Acc:HGNC:23030]","synonyms":"FLJ38866","biotype":"protein_coding","ncbi_id":"124359","summary":null,"start":80597906,"end":80804329,"strand":-1,"description":"chromodomain Y like 2 [Source:HGNC Symbol;Acc:HGNC:23030]"}, {"versioned_ensembl_gene_id":"ENSG00000260064.1","gene_symbol":"AC092332.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":80627551,"end":80628379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204704.2","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044213,"end":29045240,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000250012.1","gene_symbol":"AC079848.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":126084220,"end":126095349,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282949.1","gene_symbol":"PCMTD1P7","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51751]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107080553","summary":null,"start":29321310,"end":29321666,"strand":-1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51751]"}, {"versioned_ensembl_gene_id":"ENSG00000215586.2","gene_symbol":"AL031679.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7831798,"end":7832322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254126.6","gene_symbol":"CD8B2","gene_name":"CD8b2 molecule [Source:HGNC Symbol;Acc:HGNC:1708]","synonyms":"CD8BP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"927","summary":null,"start":106487427,"end":106506940,"strand":1,"description":"CD8b2 molecule [Source:HGNC Symbol;Acc:HGNC:1708]"}, {"versioned_ensembl_gene_id":"ENSG00000265038.1","gene_symbol":"AP001180.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10636670,"end":10637399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166123.13","gene_symbol":"GPT2","gene_name":"glutamic--pyruvic transaminase 2 [Source:HGNC Symbol;Acc:HGNC:18062]","synonyms":"ALT2","biotype":"protein_coding","ncbi_id":"84706","summary":"This gene encodes a mitochondrial alanine transaminase, a pyridoxal enzyme that catalyzes the reversible transamination between alanine and 2-oxoglutarate to generate pyruvate and glutamate. Alanine transaminases play roles in gluconeogenesis and amino acid metabolism in many tissues including skeletal muscle, kidney, and liver. Activating transcription factor 4 upregulates this gene under metabolic stress conditions in hepatocyte cell lines. A loss of function mutation in this gene has been associated with developmental encephalopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":46884378,"end":46931297,"strand":1,"description":"glutamic--pyruvic transaminase 2 [Source:HGNC Symbol;Acc:HGNC:18062]"}, {"versioned_ensembl_gene_id":"ENSG00000237215.3","gene_symbol":"DEFB131D","gene_name":"defensin beta 131D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38061]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287066","summary":null,"start":12290071,"end":12296180,"strand":-1,"description":"defensin beta 131D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:38061]"}, {"versioned_ensembl_gene_id":"ENSG00000282870.1","gene_symbol":"FRG1DP","gene_name":"FSHD region gene 1 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:51763]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102723316","summary":null,"start":29080390,"end":29102761,"strand":1,"description":"FSHD region gene 1 family member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:51763]"}, {"versioned_ensembl_gene_id":"ENSG00000280213.1","gene_symbol":"UCKL1-AS1","gene_name":"UCKL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31967]","synonyms":"UCKL1OS,UCKL1AS,UCKL1-AS,FLJ46647","biotype":"antisense_RNA","ncbi_id":"100113386","summary":null,"start":63953384,"end":63956985,"strand":1,"description":"UCKL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31967]"}, {"versioned_ensembl_gene_id":"ENSG00000279833.1","gene_symbol":"AL031846.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39133090,"end":39136760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185753.12","gene_symbol":"CXorf38","gene_name":"chromosome X open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:28589]","synonyms":"MGC39350","biotype":"protein_coding","ncbi_id":"159013","summary":null,"start":40626921,"end":40647554,"strand":-1,"description":"chromosome X open reading frame 38 [Source:HGNC Symbol;Acc:HGNC:28589]"}, {"versioned_ensembl_gene_id":"ENSG00000248358.2","gene_symbol":"AC243972.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21714795,"end":21716262,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282450.1","gene_symbol":"AC012676.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4428861,"end":4429339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244281.1","gene_symbol":"AC107302.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81366990,"end":81368021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214003.2","gene_symbol":"ATP5F1P3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39744]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644333","summary":null,"start":152749079,"end":152749735,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39744]"}, {"versioned_ensembl_gene_id":"ENSG00000284691.1","gene_symbol":"AC073111.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":150400702,"end":150412470,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284659.1","gene_symbol":"AC073869.9","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":131419665,"end":131419784,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106278.11","gene_symbol":"PTPRZ1","gene_name":"protein tyrosine phosphatase, receptor type Z1 [Source:HGNC Symbol;Acc:HGNC:9685]","synonyms":"PTPRZ,PTP18,phosphacan,RPTPB,PTPZ","biotype":"protein_coding","ncbi_id":"5803","summary":"This gene encodes a member of the receptor protein tyrosine phosphatase family. Expression of this gene is restricted to the central nervous system (CNS), and it may be involved in the regulation of specific developmental processes in the CNS. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]","start":121873089,"end":122062036,"strand":1,"description":"protein tyrosine phosphatase, receptor type Z1 [Source:HGNC Symbol;Acc:HGNC:9685]"}, {"versioned_ensembl_gene_id":"ENSG00000281815.1","gene_symbol":"AC127032.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45851975,"end":45852968,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242781.1","gene_symbol":"LINC02050","gene_name":"long intergenic non-protein coding RNA 2050 [Source:HGNC Symbol;Acc:HGNC:52890]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377175","summary":null,"start":80764897,"end":80789354,"strand":1,"description":"long intergenic non-protein coding RNA 2050 [Source:HGNC Symbol;Acc:HGNC:52890]"}, {"versioned_ensembl_gene_id":"ENSG00000165120.3","gene_symbol":"SSMEM1","gene_name":"serine rich single-pass membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29580]","synonyms":"FLJ40316,C7orf45","biotype":"protein_coding","ncbi_id":"136263","summary":null,"start":130207860,"end":130216843,"strand":1,"description":"serine rich single-pass membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29580]"}, {"versioned_ensembl_gene_id":"ENSG00000100802.14","gene_symbol":"C14orf93","gene_name":"chromosome 14 open reading frame 93 [Source:HGNC Symbol;Acc:HGNC:20162]","synonyms":"RTFC,FLJ12154","biotype":"protein_coding","ncbi_id":"60686","summary":null,"start":22985908,"end":23010166,"strand":-1,"description":"chromosome 14 open reading frame 93 [Source:HGNC Symbol;Acc:HGNC:20162]"}, {"versioned_ensembl_gene_id":"ENSG00000227373.5","gene_symbol":"AL121983.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174115300,"end":174160004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235068.9","gene_symbol":"POU5F1","gene_name":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]","synonyms":"OCT3,OTF3,MGC22487,Oct4","biotype":"protein_coding","ncbi_id":"5460","summary":"This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]","start":31242859,"end":31249234,"strand":-1,"description":"POU class 5 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9221]"}, {"versioned_ensembl_gene_id":"ENSG00000270776.1","gene_symbol":"AC012443.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152539197,"end":152539427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167104.11","gene_symbol":"BPIFB6","gene_name":"BPI fold containing family B member 6 [Source:HGNC Symbol;Acc:HGNC:16504]","synonyms":"LPLUNC6,BPIL3","biotype":"protein_coding","ncbi_id":"128859","summary":null,"start":33031648,"end":33044047,"strand":1,"description":"BPI fold containing family B member 6 [Source:HGNC Symbol;Acc:HGNC:16504]"}, {"versioned_ensembl_gene_id":"ENSG00000164287.12","gene_symbol":"CDC20B","gene_name":"cell division cycle 20B [Source:HGNC Symbol;Acc:HGNC:24222]","synonyms":"FLJ37927","biotype":"protein_coding","ncbi_id":"166979","summary":null,"start":55112995,"end":55173175,"strand":-1,"description":"cell division cycle 20B [Source:HGNC Symbol;Acc:HGNC:24222]"}, {"versioned_ensembl_gene_id":"ENSG00000117262.18","gene_symbol":"GPR89A","gene_name":"G protein-coupled receptor 89A [Source:HGNC Symbol;Acc:HGNC:31984]","synonyms":"UNQ192","biotype":"protein_coding","ncbi_id":"653519","summary":"GPR89A is a nearly identical copy of the GPR89B gene (MIM 612806).[supplied by OMIM, Jun 2009]","start":145607990,"end":145670648,"strand":1,"description":"G protein-coupled receptor 89A [Source:HGNC Symbol;Acc:HGNC:31984]"}, {"versioned_ensembl_gene_id":"ENSG00000164294.13","gene_symbol":"GPX8","gene_name":"glutathione peroxidase 8 (putative) [Source:HGNC Symbol;Acc:HGNC:33100]","synonyms":"UNQ847,EPLA847","biotype":"protein_coding","ncbi_id":"493869","summary":null,"start":55160118,"end":55167071,"strand":1,"description":"glutathione peroxidase 8 (putative) [Source:HGNC Symbol;Acc:HGNC:33100]"}, {"versioned_ensembl_gene_id":"ENSG00000230777.1","gene_symbol":"RPS29P5","gene_name":"ribosomal protein S29 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35584]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271124","summary":null,"start":175921975,"end":175922145,"strand":1,"description":"ribosomal protein S29 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:35584]"}, {"versioned_ensembl_gene_id":"ENSG00000120337.8","gene_symbol":"TNFSF18","gene_name":"TNF superfamily member 18 [Source:HGNC Symbol;Acc:HGNC:11932]","synonyms":"TL6,hGITRL,AITRL","biotype":"protein_coding","ncbi_id":"8995","summary":"The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for receptor TNFRSF18/AITR/GITR. It has been shown to modulate T lymphocyte survival in peripheral tissues. This cytokine is also found to be expressed in endothelial cells, and is thought to be important for interaction between T lymphocytes and endothelial cells. [provided by RefSeq, Jul 2008]","start":173039960,"end":173050963,"strand":-1,"description":"TNF superfamily member 18 [Source:HGNC Symbol;Acc:HGNC:11932]"}, {"versioned_ensembl_gene_id":"ENSG00000250272.1","gene_symbol":"TRMT112P1","gene_name":"tRNA methyltransferase subunit 11-2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44020]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288861","summary":null,"start":116378919,"end":116379269,"strand":1,"description":"tRNA methyltransferase subunit 11-2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44020]"}, {"versioned_ensembl_gene_id":"ENSG00000270394.4","gene_symbol":"MTRNR2L13","gene_name":"MT-RNR2-like 13 [Source:HGNC Symbol;Acc:HGNC:37170]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463500","summary":null,"start":116298876,"end":116300320,"strand":1,"description":"MT-RNR2-like 13 [Source:HGNC Symbol;Acc:HGNC:37170]"}, {"versioned_ensembl_gene_id":"ENSG00000271869.1","gene_symbol":"AC026979.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30155830,"end":30156232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206560.11","gene_symbol":"ANKRD28","gene_name":"ankyrin repeat domain 28 [Source:HGNC Symbol;Acc:HGNC:29024]","synonyms":"PPP1R65,PP6-ARS-A,PITK,KIAA0379","biotype":"protein_coding","ncbi_id":"23243","summary":null,"start":15667236,"end":15859771,"strand":-1,"description":"ankyrin repeat domain 28 [Source:HGNC Symbol;Acc:HGNC:29024]"}, {"versioned_ensembl_gene_id":"ENSG00000228712.2","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"SDR30C1,HKE6,D6S2245E,RING2,H2-KE6,KE6,FABGL","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33126266,"end":33128451,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000238205.3","gene_symbol":"MPC1L","gene_name":"mitochondrial pyruvate carrier 1 like [Source:HGNC Symbol;Acc:HGNC:44205]","synonyms":null,"biotype":"protein_coding","ncbi_id":"347411","summary":null,"start":40623566,"end":40624136,"strand":1,"description":"mitochondrial pyruvate carrier 1 like [Source:HGNC Symbol;Acc:HGNC:44205]"}, {"versioned_ensembl_gene_id":"ENSG00000140835.9","gene_symbol":"CHST4","gene_name":"carbohydrate sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:1972]","synonyms":"LSST,HEC-GLCNAC-6-ST","biotype":"protein_coding","ncbi_id":"10164","summary":"This gene encodes an N-acetylglucosamine 6-O sulfotransferase. The encoded enzyme transfers sulfate from 3'phosphoadenosine 5'phospho-sulfate to the 6-hydroxyl group of N-acetylglucosamine on glycoproteins. This protein is localized to the Golgi and is involved in the modification of glycan structures on ligands of the lymphocyte homing receptor L-selectin. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]","start":71525233,"end":71538746,"strand":1,"description":"carbohydrate sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:1972]"}, {"versioned_ensembl_gene_id":"ENSG00000173214.5","gene_symbol":"MFSD4B","gene_name":"major facilitator superfamily domain containing 4B [Source:HGNC Symbol;Acc:HGNC:21053]","synonyms":"MGC33953,KIAA1919","biotype":"protein_coding","ncbi_id":"91749","summary":null,"start":111259348,"end":111271167,"strand":1,"description":"major facilitator superfamily domain containing 4B [Source:HGNC Symbol;Acc:HGNC:21053]"}, {"versioned_ensembl_gene_id":"ENSG00000149930.17","gene_symbol":"TAOK2","gene_name":"TAO kinase 2 [Source:HGNC Symbol;Acc:HGNC:16835]","synonyms":"TAO2,TAO1,PSK1,PSK,MAP3K17,KIAA0881","biotype":"protein_coding","ncbi_id":"9344","summary":"This gene encodes a serine/threonine protein kinase that is involved in many different processes, including, cell signaling, microtubule organization and stability, and apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]","start":29973641,"end":29992261,"strand":1,"description":"TAO kinase 2 [Source:HGNC Symbol;Acc:HGNC:16835]"}, {"versioned_ensembl_gene_id":"ENSG00000259922.1","gene_symbol":"AC023825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57013071,"end":57014100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269971.1","gene_symbol":"AL020997.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":27773858,"end":27774041,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248629.1","gene_symbol":"AC092608.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":156841359,"end":156842236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270966.1","gene_symbol":"AC087763.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8933721,"end":8934006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187642.9","gene_symbol":"PERM1","gene_name":"PPARGC1 and ESRR induced regulator, muscle 1 [Source:HGNC Symbol;Acc:HGNC:28208]","synonyms":"RP11-54O7.8,Perm1,MGC13275,C1orf170","biotype":"protein_coding","ncbi_id":"84808","summary":null,"start":975204,"end":982093,"strand":-1,"description":"PPARGC1 and ESRR induced regulator, muscle 1 [Source:HGNC Symbol;Acc:HGNC:28208]"}, {"versioned_ensembl_gene_id":"ENSG00000241572.1","gene_symbol":"PRICKLE2-AS1","gene_name":"PRICKLE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40916]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652759","summary":null,"start":64099273,"end":64101122,"strand":1,"description":"PRICKLE2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40916]"}, {"versioned_ensembl_gene_id":"ENSG00000134020.7","gene_symbol":"PEBP4","gene_name":"phosphatidylethanolamine binding protein 4 [Source:HGNC Symbol;Acc:HGNC:28319]","synonyms":"MGC22776,hPEBP4,CORK1","biotype":"protein_coding","ncbi_id":"157310","summary":"The phosphatidylethanolamine (PE)-binding proteins, including PEBP4, are an evolutionarily conserved family of proteins with pivotal biologic functions, such as lipid binding and inhibition of serine proteases (Wang et al., 2004 [PubMed 15302887]).[supplied by OMIM, Dec 2008]","start":22713251,"end":23000000,"strand":-1,"description":"phosphatidylethanolamine binding protein 4 [Source:HGNC Symbol;Acc:HGNC:28319]"}, {"versioned_ensembl_gene_id":"ENSG00000254923.1","gene_symbol":"AC130366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12128107,"end":12129298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078898.6","gene_symbol":"BPIFB2","gene_name":"BPI fold containing family B member 2 [Source:HGNC Symbol;Acc:HGNC:16177]","synonyms":"LPLUNC2,dJ726C3.2,C20orf184,BPIL1","biotype":"protein_coding","ncbi_id":"80341","summary":"This gene encodes a member of the lipid transfer/lipopolysaccharide binding protein (LT/LBP) gene family. It is highly expressed in hypertrophic tonsils. This gene and three other members of the LT/LBP gene family form a cluster on the long arm of chromosome 20. [provided by RefSeq, Jul 2008]","start":33007600,"end":33023709,"strand":1,"description":"BPI fold containing family B member 2 [Source:HGNC Symbol;Acc:HGNC:16177]"}, {"versioned_ensembl_gene_id":"ENSG00000227713.1","gene_symbol":"AC092159.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":724966,"end":731224,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253125.1","gene_symbol":"AC055854.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22690150,"end":22798616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253777.1","gene_symbol":"AC026616.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74804287,"end":74804811,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253341.1","gene_symbol":"AC115837.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74603244,"end":74604244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253616.5","gene_symbol":"AC107959.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23071377,"end":23074488,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064218.4","gene_symbol":"DMRT3","gene_name":"doublesex and mab-3 related transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:13909]","synonyms":"DMRTA3","biotype":"protein_coding","ncbi_id":"58524","summary":null,"start":976964,"end":991731,"strand":1,"description":"doublesex and mab-3 related transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:13909]"}, {"versioned_ensembl_gene_id":"ENSG00000138764.14","gene_symbol":"CCNG2","gene_name":"cyclin G2 [Source:HGNC Symbol;Acc:HGNC:1593]","synonyms":null,"biotype":"protein_coding","ncbi_id":"901","summary":"The eukaryotic cell cycle is governed by cyclin-dependent protein kinases (CDKs) whose activities are regulated by cyclins and CDK inhibitors. The 8 species of cyclins reported in mammals, cyclins A through H, share a conserved amino acid sequence of about 90 residues called the cyclin box. The amino acid sequence of cyclin G is well conserved among mammals. The nucleotide sequence of cyclin G1 and cyclin G2 are 53% identical. Unlike cyclin G1, cyclin G2 contains a C-terminal PEST protein destabilization motif, suggesting that cyclin G2 expression is tightly regulated through the cell cycle. [provided by RefSeq, Jul 2008]","start":77157151,"end":77433388,"strand":1,"description":"cyclin G2 [Source:HGNC Symbol;Acc:HGNC:1593]"}, {"versioned_ensembl_gene_id":"ENSG00000261293.1","gene_symbol":"AC007601.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12093627,"end":12095307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272901.5","gene_symbol":"SMDT1","gene_name":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]","synonyms":"dJ186O1.1,DDDD,C22orf32,EMRE","biotype":"protein_coding","ncbi_id":"91689","summary":"This gene encodes a core regulatory component of a calcium channel in the mitochondrial inner membrane. [provided by RefSeq, Apr 2017]","start":42079691,"end":42124100,"strand":1,"description":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]"}, {"versioned_ensembl_gene_id":"ENSG00000280128.1","gene_symbol":"AL662795.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30282349,"end":30286054,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125355.15","gene_symbol":"TMEM255A","gene_name":"transmembrane protein 255A [Source:HGNC Symbol;Acc:HGNC:26086]","synonyms":"FLJ20716,FAM70A","biotype":"protein_coding","ncbi_id":"55026","summary":null,"start":120258650,"end":120311556,"strand":-1,"description":"transmembrane protein 255A [Source:HGNC Symbol;Acc:HGNC:26086]"}, {"versioned_ensembl_gene_id":"ENSG00000248167.7","gene_symbol":"TRIM39-RPP21","gene_name":"TRIM39-RPP21 readthrough [Source:HGNC Symbol;Acc:HGNC:38845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"202658","summary":"This locus represents naturally occurring read-through transcription between the neighboring TRIM39 (tripartite motif-containing 39) and RPP21 (ribonuclease P/MRP 21kDa subunit) genes on chromosome 6. The read-through transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Nov 2010]","start":30328907,"end":30346854,"strand":1,"description":"TRIM39-RPP21 readthrough [Source:HGNC Symbol;Acc:HGNC:38845]"}, {"versioned_ensembl_gene_id":"ENSG00000284554.1","gene_symbol":"AL022318.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":39014363,"end":39033276,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247626.4","gene_symbol":"MARS2","gene_name":"methionyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25133]","synonyms":"SPAX3,mtMetRS","biotype":"protein_coding","ncbi_id":"92935","summary":"This gene produces a mitochondrial methionyl-tRNA synthetase protein that is encoded by the nuclear genome and imported to the mitochondrion. This protein likely functions as a monomer and is predicted to localize to the mitochondrial matrix. Mutations in this gene are associated with the autosomal recessive neurodegenerative disease spastic ataxia-3 (SPAX3). [provided by RefSeq, Apr 2014]","start":197705369,"end":197708387,"strand":1,"description":"methionyl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:25133]"}, {"versioned_ensembl_gene_id":"ENSG00000227746.9","gene_symbol":"C4A","gene_name":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]","synonyms":"C4A2,C4A6,CO4,C4,C4A4,C4S,RG,C4A3,C4B,CPAMD2","biotype":"protein_coding","ncbi_id":"720","summary":"This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain is cleaved to release C4 anaphylatoxin, an antimicrobial peptide and a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":32091205,"end":32111862,"strand":1,"description":"complement C4A (Rodgers blood group) [Source:HGNC Symbol;Acc:HGNC:1323]"}, {"versioned_ensembl_gene_id":"ENSG00000225540.1","gene_symbol":"C4A-AS1","gene_name":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106478955","summary":null,"start":32109173,"end":32112702,"strand":-1,"description":"C4A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39753]"}, {"versioned_ensembl_gene_id":"ENSG00000225169.1","gene_symbol":"BRI3P1","gene_name":"brain protein I3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33533]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730010","summary":null,"start":100213293,"end":100213670,"strand":1,"description":"brain protein I3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33533]"}, {"versioned_ensembl_gene_id":"ENSG00000277930.1","gene_symbol":"AC010722.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4993858,"end":4999650,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214424.5","gene_symbol":"FAM149B1P1","gene_name":"family with sequence similarity 149 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31735]","synonyms":"KIAA0974P,FAM149B2","biotype":"processed_pseudogene","ncbi_id":"388181","summary":null,"start":96756987,"end":96758596,"strand":1,"description":"family with sequence similarity 149 member B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31735]"}, {"versioned_ensembl_gene_id":"ENSG00000259312.1","gene_symbol":"AC087477.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96438570,"end":96444266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198821.10","gene_symbol":"CD247","gene_name":"CD247 molecule [Source:HGNC Symbol;Acc:HGNC:1677]","synonyms":"CD3Z,CD3Q,CD3H","biotype":"protein_coding","ncbi_id":"919","summary":"The protein encoded by this gene is T-cell receptor zeta, which together with T-cell receptor alpha/beta and gamma/delta heterodimers, and with CD3-gamma, -delta and -epsilon, forms the T-cell receptor-CD3 complex. The zeta chain plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. Low expression of the antigen results in impaired immune response. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":167430640,"end":167518610,"strand":-1,"description":"CD247 molecule [Source:HGNC Symbol;Acc:HGNC:1677]"}, {"versioned_ensembl_gene_id":"ENSG00000227371.1","gene_symbol":"AC074085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121419072,"end":121419845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257228.5","gene_symbol":"AC090531.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41409467,"end":41473510,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279176.1","gene_symbol":"AC079316.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":104552073,"end":104553447,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231187.2","gene_symbol":"AL356056.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46582782,"end":46598145,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260014.1","gene_symbol":"LSM3P5","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44350]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100303743","summary":null,"start":78355529,"end":78355834,"strand":1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44350]"}, {"versioned_ensembl_gene_id":"ENSG00000236842.1","gene_symbol":"AC010997.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75430571,"end":75431588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278120.1","gene_symbol":"KIR2DS1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]","synonyms":"CD158H,EB6ActII,EB6ActI,EB6ActI,CD158H,EB6ActII","biotype":"protein_coding","ncbi_id":"3806","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54504993,"end":54518921,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6333]"}, {"versioned_ensembl_gene_id":"ENSG00000237732.9","gene_symbol":"AC010980.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":222318275,"end":222352989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274739.1","gene_symbol":"KIR2DS5","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 5 [Source:HGNC Symbol;Acc:HGNC:6337]","synonyms":"nkat9,CD158G","biotype":"protein_coding","ncbi_id":"3810","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54488004,"end":54503024,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 5 [Source:HGNC Symbol;Acc:HGNC:6337]"}, {"versioned_ensembl_gene_id":"ENSG00000213310.3","gene_symbol":"CYCSP19","gene_name":"cytochrome c, somatic pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:24392]","synonyms":"HCP19","biotype":"processed_pseudogene","ncbi_id":"360174","summary":null,"start":121398452,"end":121398767,"strand":1,"description":"cytochrome c, somatic pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:24392]"}, {"versioned_ensembl_gene_id":"ENSG00000165966.14","gene_symbol":"PDZRN4","gene_name":"PDZ domain containing ring finger 4 [Source:HGNC Symbol;Acc:HGNC:30552]","synonyms":"LNX4,IMAGE5767589,FLJ33777,DKFZp434B0417","biotype":"protein_coding","ncbi_id":"29951","summary":null,"start":41188448,"end":41574590,"strand":1,"description":"PDZ domain containing ring finger 4 [Source:HGNC Symbol;Acc:HGNC:30552]"}, {"versioned_ensembl_gene_id":"ENSG00000278582.1","gene_symbol":"AC027139.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34520608,"end":34521791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231777.1","gene_symbol":"MTND4P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42208]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873243","summary":null,"start":131372294,"end":131373650,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42208]"}, {"versioned_ensembl_gene_id":"ENSG00000204121.2","gene_symbol":"ECEL1P1","gene_name":"endothelin converting enzyme like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14017]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100131546","summary":null,"start":232415818,"end":232419816,"strand":-1,"description":"endothelin converting enzyme like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14017]"}, {"versioned_ensembl_gene_id":"ENSG00000138741.10","gene_symbol":"TRPC3","gene_name":"transient receptor potential cation channel subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:12335]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7222","summary":"The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":121879027,"end":121951754,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 3 [Source:HGNC Symbol;Acc:HGNC:12335]"}, {"versioned_ensembl_gene_id":"ENSG00000138653.9","gene_symbol":"NDST4","gene_name":"N-deacetylase and N-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:20779]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64579","summary":null,"start":114827763,"end":115113876,"strand":-1,"description":"N-deacetylase and N-sulfotransferase 4 [Source:HGNC Symbol;Acc:HGNC:20779]"}, {"versioned_ensembl_gene_id":"ENSG00000272736.5","gene_symbol":"AC005323.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10383132,"end":10537862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243156.7","gene_symbol":"MICAL3","gene_name":"microtubule associated monooxygenase, calponin and LIM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24694]","synonyms":"KIAA0819","biotype":"protein_coding","ncbi_id":"57553","summary":null,"start":17787649,"end":18024559,"strand":-1,"description":"microtubule associated monooxygenase, calponin and LIM domain containing 3 [Source:HGNC Symbol;Acc:HGNC:24694]"}, {"versioned_ensembl_gene_id":"ENSG00000277616.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54814388,"end":54828892,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000259275.2","gene_symbol":"AC087477.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96354237,"end":96403803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268742.1","gene_symbol":"AC010503.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6552358,"end":6554494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231203.1","gene_symbol":"KRT8P10","gene_name":"keratin 8 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:33364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344320","summary":null,"start":183071040,"end":183072486,"strand":-1,"description":"keratin 8 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:33364]"}, {"versioned_ensembl_gene_id":"ENSG00000255052.4","gene_symbol":"FAM66D","gene_name":"family with sequence similarity 66 member D [Source:HGNC Symbol;Acc:HGNC:24159]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100132923","summary":null,"start":12115782,"end":12177550,"strand":1,"description":"family with sequence similarity 66 member D [Source:HGNC Symbol;Acc:HGNC:24159]"}, {"versioned_ensembl_gene_id":"ENSG00000282382.1","gene_symbol":"AP005902.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39712389,"end":39712765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144407.9","gene_symbol":"PTH2R","gene_name":"parathyroid hormone 2 receptor [Source:HGNC Symbol;Acc:HGNC:9609]","synonyms":"PTHR2","biotype":"protein_coding","ncbi_id":"5746","summary":"The protein encoded by this gene is a member of the G-protein coupled receptor 2 family. This protein is a receptor for parathyroid hormone (PTH). This receptor is more selective in ligand recognition and has a more specific tissue distribution compared to parathyroid hormone receptor 1 (PTHR1). It is activated only by PTH and not by parathyroid hormone-like hormone (PTHLH) and is particularly abundant in brain and pancreas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":208359714,"end":208854503,"strand":1,"description":"parathyroid hormone 2 receptor [Source:HGNC Symbol;Acc:HGNC:9609]"}, {"versioned_ensembl_gene_id":"ENSG00000280745.1","gene_symbol":"AC208386.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69418516,"end":69419862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277111.3","gene_symbol":"PLEKHM1","gene_name":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]","synonyms":"KIAA0356","biotype":"protein_coding","ncbi_id":"9842","summary":"The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]","start":45435832,"end":45490687,"strand":-1,"description":"pleckstrin homology and RUN domain containing M1 [Source:HGNC Symbol;Acc:HGNC:29017]"}, {"versioned_ensembl_gene_id":"ENSG00000254086.1","gene_symbol":"AC131254.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29864644,"end":29871661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263091.2","gene_symbol":"KRTAP2-4","gene_name":"keratin associated protein 2-4 [Source:HGNC Symbol;Acc:HGNC:18891]","synonyms":"KAP2.4","biotype":"protein_coding","ncbi_id":"85294","summary":"This protein is a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This protein is a member of the high sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21. [provided by RefSeq, Jul 2008]","start":41065346,"end":41066109,"strand":-1,"description":"keratin associated protein 2-4 [Source:HGNC Symbol;Acc:HGNC:18891]"}, {"versioned_ensembl_gene_id":"ENSG00000225246.1","gene_symbol":"RPS2P1","gene_name":"ribosomal protein S2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16580]","synonyms":"dJ64K7.1","biotype":"processed_pseudogene","ncbi_id":"140755","summary":null,"start":34122470,"end":34123290,"strand":1,"description":"ribosomal protein S2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16580]"}, {"versioned_ensembl_gene_id":"ENSG00000116106.11","gene_symbol":"EPHA4","gene_name":"EPH receptor A4 [Source:HGNC Symbol;Acc:HGNC:3388]","synonyms":"TYRO1,Hek8","biotype":"protein_coding","ncbi_id":"2043","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":221418027,"end":221574202,"strand":-1,"description":"EPH receptor A4 [Source:HGNC Symbol;Acc:HGNC:3388]"}, {"versioned_ensembl_gene_id":"ENSG00000242531.1","gene_symbol":"AC083798.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":122416882,"end":122417012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259505.1","gene_symbol":"AC009268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33990686,"end":33992048,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278472.1","gene_symbol":"AC009268.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":33972059,"end":33972515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138075.11","gene_symbol":"ABCG5","gene_name":"ATP binding cassette subfamily G member 5 [Source:HGNC Symbol;Acc:HGNC:13886]","synonyms":"STSL","biotype":"protein_coding","ncbi_id":"64240","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008]","start":43812472,"end":43838865,"strand":-1,"description":"ATP binding cassette subfamily G member 5 [Source:HGNC Symbol;Acc:HGNC:13886]"}, {"versioned_ensembl_gene_id":"ENSG00000176700.19","gene_symbol":"SCAND2P","gene_name":"SCAN domain containing 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:10567]","synonyms":"SCAND2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"54581","summary":null,"start":84631451,"end":84647478,"strand":1,"description":"SCAN domain containing 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:10567]"}, {"versioned_ensembl_gene_id":"ENSG00000137098.13","gene_symbol":"SPAG8","gene_name":"sperm associated antigen 8 [Source:HGNC Symbol;Acc:HGNC:14105]","synonyms":"hSMP-1,HSD-1,CT142,BS-84,SPAG3","biotype":"protein_coding","ncbi_id":"26206","summary":"The correlation of anti-sperm antibodies with cases of unexplained infertility implicates a role for these antibodies in blocking fertilization. Improved diagnosis and treatment of immunologic infertility, as well as identification of proteins for targeted contraception, are dependent on the identification and characterization of relevant sperm antigens. The protein encoded by this gene is recognized by sperm agglutinating antibodies from an infertile woman. This protein is localized in germ cells of the testis at all stages of spermatogenesis and is localized to the acrosomal region of mature spermatozoa. This protein interacts with ACT (activator of CREM in testis) and may play a role in CREM (cAMP response element modulator)-ACT-mediated gene transcription during spermatogenesis. This protein may also play a role in spermatogenesis by regulating microtubule formation and cell division. Alternatively spliced variants that encode different protein isoforms have been described but the full-length sequences of only two have been determined. [provided by RefSeq, Jul 2012]","start":35808045,"end":35812272,"strand":-1,"description":"sperm associated antigen 8 [Source:HGNC Symbol;Acc:HGNC:14105]"}, {"versioned_ensembl_gene_id":"ENSG00000211665.3","gene_symbol":"IGLV3-16","gene_name":"immunoglobulin lambda variable 3-16 [Source:HGNC Symbol;Acc:HGNC:5901]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28799","summary":null,"start":22747383,"end":22747921,"strand":1,"description":"immunoglobulin lambda variable 3-16 [Source:HGNC Symbol;Acc:HGNC:5901]"}, {"versioned_ensembl_gene_id":"ENSG00000105640.12","gene_symbol":"RPL18A","gene_name":"ribosomal protein L18a [Source:HGNC Symbol;Acc:HGNC:10311]","synonyms":"L18A","biotype":"protein_coding","ncbi_id":"6142","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a member of the L18AE family of ribosomal proteins that is a component of the 60S subunit. The encoded protein may play a role in viral replication by interacting with the hepatitis C virus internal ribosome entry site (IRES). This gene is co-transcribed with the U68 snoRNA, located within the third intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed throughout the genome. [provided by RefSeq, Jul 2012]","start":17859876,"end":17864153,"strand":1,"description":"ribosomal protein L18a [Source:HGNC Symbol;Acc:HGNC:10311]"}, {"versioned_ensembl_gene_id":"ENSG00000211663.2","gene_symbol":"IGLV3-19","gene_name":"immunoglobulin lambda variable 3-19 [Source:HGNC Symbol;Acc:HGNC:5903]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28797","summary":null,"start":22720623,"end":22721145,"strand":1,"description":"immunoglobulin lambda variable 3-19 [Source:HGNC Symbol;Acc:HGNC:5903]"}, {"versioned_ensembl_gene_id":"ENSG00000259856.1","gene_symbol":"RAB43P1","gene_name":"RAB43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33153]","synonyms":"RAB43P,RAB41P","biotype":"processed_pseudogene","ncbi_id":"440375","summary":null,"start":46626404,"end":46626992,"strand":-1,"description":"RAB43 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33153]"}, {"versioned_ensembl_gene_id":"ENSG00000099810.18","gene_symbol":"MTAP","gene_name":"methylthioadenosine phosphorylase [Source:HGNC Symbol;Acc:HGNC:7413]","synonyms":"MSAP,c86fus","biotype":"protein_coding","ncbi_id":"4507","summary":"This gene encodes an enzyme that plays a major role in polyamine metabolism and is important for the salvage of both adenine and methionine. The encoded enzyme is deficient in many cancers because this gene and the tumor suppressor p16 gene are co-deleted. Multiple alternatively spliced transcript variants have been described for this gene, but their full-length natures remain unknown. [provided by RefSeq, Jul 2008]","start":21802543,"end":21937651,"strand":1,"description":"methylthioadenosine phosphorylase [Source:HGNC Symbol;Acc:HGNC:7413]"}, {"versioned_ensembl_gene_id":"ENSG00000234632.1","gene_symbol":"NECAP1P2","gene_name":"NECAP endocytosis associated 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479026","summary":null,"start":74350069,"end":74351009,"strand":1,"description":"NECAP endocytosis associated 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43913]"}, {"versioned_ensembl_gene_id":"ENSG00000156958.14","gene_symbol":"GALK2","gene_name":"galactokinase 2 [Source:HGNC Symbol;Acc:HGNC:4119]","synonyms":"GK2","biotype":"protein_coding","ncbi_id":"2585","summary":"This gene encodes a highly efficient N-acetylgalactosamine (GalNAc) kinase, which has galactokinase activity when galactose is present at high concentrations. The encoded protein is a member of the GHMP kinase family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2017]","start":49155656,"end":49367869,"strand":1,"description":"galactokinase 2 [Source:HGNC Symbol;Acc:HGNC:4119]"}, {"versioned_ensembl_gene_id":"ENSG00000228843.2","gene_symbol":"AL133410.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35756712,"end":35757940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211659.2","gene_symbol":"IGLV3-25","gene_name":"immunoglobulin lambda variable 3-25 [Source:HGNC Symbol;Acc:HGNC:5908]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28793","summary":null,"start":22686726,"end":22687271,"strand":1,"description":"immunoglobulin lambda variable 3-25 [Source:HGNC Symbol;Acc:HGNC:5908]"}, {"versioned_ensembl_gene_id":"ENSG00000258077.2","gene_symbol":"AC078923.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":75563202,"end":75984015,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258091.1","gene_symbol":"AC011611.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75926213,"end":75926467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225492.6","gene_symbol":"GBP1P1","gene_name":"guanylate binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39561]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"400759","summary":null,"start":89407679,"end":89426243,"strand":1,"description":"guanylate binding protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39561]"}, {"versioned_ensembl_gene_id":"ENSG00000226703.1","gene_symbol":"NPM1P4","gene_name":"nucleophosmin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:7924]","synonyms":"NPMP4,NG4-5","biotype":"processed_pseudogene","ncbi_id":"100128903","summary":null,"start":27696393,"end":27697204,"strand":-1,"description":"nucleophosmin 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:7924]"}, {"versioned_ensembl_gene_id":"ENSG00000204209.11","gene_symbol":"DAXX","gene_name":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]","synonyms":"DAP6","biotype":"protein_coding","ncbi_id":"1616","summary":"This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]","start":33318558,"end":33329286,"strand":-1,"description":"death domain associated protein [Source:HGNC Symbol;Acc:HGNC:2681]"}, {"versioned_ensembl_gene_id":"ENSG00000260610.1","gene_symbol":"AC142086.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32931768,"end":32932569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260921.1","gene_symbol":"AC142086.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32995537,"end":32996770,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270698.1","gene_symbol":"AC018695.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85814425,"end":85815062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271307.3","gene_symbol":"AF146191.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189979902,"end":189982379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225796.2","gene_symbol":"MTND4P23","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42210]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873245","summary":null,"start":201213298,"end":201214660,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42210]"}, {"versioned_ensembl_gene_id":"ENSG00000227348.1","gene_symbol":"MTND5P25","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42287]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873263","summary":null,"start":201212283,"end":201213081,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:42287]"}, {"versioned_ensembl_gene_id":"ENSG00000249883.1","gene_symbol":"AC104803.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180731164,"end":180759038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224750.6","gene_symbol":"AL391704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90454170,"end":90502968,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238291.1","gene_symbol":"AL391704.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90462717,"end":90467952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227684.2","gene_symbol":"CROCCP4","gene_name":"ciliary rootlet coiled-coil, rootletin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43864]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421113","summary":null,"start":16740280,"end":16750968,"strand":1,"description":"ciliary rootlet coiled-coil, rootletin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43864]"}, {"versioned_ensembl_gene_id":"ENSG00000138131.3","gene_symbol":"LOXL4","gene_name":"lysyl oxidase like 4 [Source:HGNC Symbol;Acc:HGNC:17171]","synonyms":"LOXC,FLJ21889","biotype":"protein_coding","ncbi_id":"84171","summary":"This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. [provided by RefSeq, Jul 2008]","start":98247690,"end":98268250,"strand":-1,"description":"lysyl oxidase like 4 [Source:HGNC Symbol;Acc:HGNC:17171]"}, {"versioned_ensembl_gene_id":"ENSG00000237601.1","gene_symbol":"AP000358.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24703348,"end":24703503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227443.2","gene_symbol":"AL137022.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21638285,"end":21638676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266456.1","gene_symbol":"AP001178.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":650229,"end":652843,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282271.1","gene_symbol":"AL031601.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42228517,"end":42262638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224334.1","gene_symbol":"AP000357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":24686923,"end":24688087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230373.8","gene_symbol":"GOLGA6L5P","gene_name":"golgin A6 family-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:30472]","synonyms":"GOLGA6L8,GOLGA6L5,FLJ40113,FLJ35171","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"374650","summary":null,"start":84507885,"end":84516814,"strand":-1,"description":"golgin A6 family-like 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:30472]"}, {"versioned_ensembl_gene_id":"ENSG00000249831.2","gene_symbol":"AC093725.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57720035,"end":57724655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228812.7","gene_symbol":"LAMA5-AS1","gene_name":"LAMA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40334]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928158","summary":null,"start":62352995,"end":62356480,"strand":1,"description":"LAMA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40334]"}, {"versioned_ensembl_gene_id":"ENSG00000238271.2","gene_symbol":"IFNWP19","gene_name":"interferon omega 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:5451]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3474","summary":null,"start":21455484,"end":21456049,"strand":1,"description":"interferon omega 1 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:5451]"}, {"versioned_ensembl_gene_id":"ENSG00000174611.11","gene_symbol":"KY","gene_name":"kyphoscoliosis peptidase [Source:HGNC Symbol;Acc:HGNC:26576]","synonyms":"FLJ33207","biotype":"protein_coding","ncbi_id":"339855","summary":"The protein encoded by this gene belongs to the transglutaminase-like superfamily. The protein is involved in the function, maturation and stabilization of the neuromuscular junction and may be required for normal muscle growth. Mutations in this gene are associated with myopathy, myofibrillar, 7. [provided by RefSeq, Apr 2017]","start":134603138,"end":134651636,"strand":-1,"description":"kyphoscoliosis peptidase [Source:HGNC Symbol;Acc:HGNC:26576]"}, {"versioned_ensembl_gene_id":"ENSG00000174007.7","gene_symbol":"CEP19","gene_name":"centrosomal protein 19 [Source:HGNC Symbol;Acc:HGNC:28209]","synonyms":"MGC14126,C3orf34","biotype":"protein_coding","ncbi_id":"84984","summary":"The protein encoded by this gene localizes to centrosomes and primary cilia and co-localizes with a marker for the mother centriole. This gene resides in a region of human chromosome 3 that is linked to morbid obesity. A homozygous knockout of the orthologous gene in mouse resulted in mice with morbid obesity, hyperphagy, glucose intolerance, and insulin resistance. Mutations in this gene cause morbid obesity and spermatogenic failure (MOSPGF). This gene has a pseudogene on human chromosome 2. [provided by RefSeq, Apr 2014]","start":196706277,"end":196712293,"strand":-1,"description":"centrosomal protein 19 [Source:HGNC Symbol;Acc:HGNC:28209]"}, {"versioned_ensembl_gene_id":"ENSG00000280197.1","gene_symbol":"C18orf12","gene_name":"chromosome 18 open reading frame 12 [Source:HGNC Symbol;Acc:HGNC:24918]","synonyms":"HsT2508,HEIL1","biotype":"TEC","ncbi_id":"84322","summary":null,"start":48252301,"end":48252837,"strand":1,"description":"chromosome 18 open reading frame 12 [Source:HGNC Symbol;Acc:HGNC:24918]"}, {"versioned_ensembl_gene_id":"ENSG00000129226.13","gene_symbol":"CD68","gene_name":"CD68 molecule [Source:HGNC Symbol;Acc:HGNC:1693]","synonyms":"SCARD1,macrosialin,LAMP4,GP110,DKFZp686M18236","biotype":"protein_coding","ncbi_id":"968","summary":"This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages. It is a member of the lysosomal/endosomal-associated membrane glycoprotein (LAMP) family. The protein primarily localizes to lysosomes and endosomes with a smaller fraction circulating to the cell surface. It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue- and organ-specific lectins or selectins. The protein is also a member of the scavenger receptor family. Scavenger receptors typically function to clear cellular debris, promote phagocytosis, and mediate the recruitment and activation of macrophages. Alternative splicing results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]","start":7579467,"end":7582113,"strand":1,"description":"CD68 molecule [Source:HGNC Symbol;Acc:HGNC:1693]"}, {"versioned_ensembl_gene_id":"ENSG00000243920.2","gene_symbol":"RPS26P24","gene_name":"ribosomal protein S26 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36917]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271113","summary":null,"start":57352999,"end":57353329,"strand":-1,"description":"ribosomal protein S26 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36917]"}, {"versioned_ensembl_gene_id":"ENSG00000171984.14","gene_symbol":"C20orf196","gene_name":"chromosome 20 open reading frame 196 [Source:HGNC Symbol;Acc:HGNC:26318]","synonyms":"FLJ25067","biotype":"protein_coding","ncbi_id":"149840","summary":null,"start":5750393,"end":5863912,"strand":1,"description":"chromosome 20 open reading frame 196 [Source:HGNC Symbol;Acc:HGNC:26318]"}, {"versioned_ensembl_gene_id":"ENSG00000281583.1","gene_symbol":"AC233280.13","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104980.7","gene_symbol":"TIMM44","gene_name":"translocase of inner mitochondrial membrane 44 [Source:HGNC Symbol;Acc:HGNC:17316]","synonyms":"TIM44","biotype":"protein_coding","ncbi_id":"10469","summary":"This gene encodes a peripheral membrane protein associated with the mitochondrial inner membrane translocase, which functions in the import of proteins across the mitochondrial inner membrane and into the mitochondrial matrix. The encoded protein mediates binding of mitochondrial heat shock protein 70 to the translocase of inner mitochondrial membrane 23 (TIM23) complex. Expression of this gene is upregulated in kidney in a mouse model of diabetes. A mutation in this gene is associated with familial oncocytic thyroid carcinoma. [provided by RefSeq, Jul 2016]","start":7926718,"end":7943920,"strand":-1,"description":"translocase of inner mitochondrial membrane 44 [Source:HGNC Symbol;Acc:HGNC:17316]"}, {"versioned_ensembl_gene_id":"ENSG00000115762.16","gene_symbol":"PLEKHB2","gene_name":"pleckstrin homology domain containing B2 [Source:HGNC Symbol;Acc:HGNC:19236]","synonyms":"FLJ20783,EVT2","biotype":"protein_coding","ncbi_id":"55041","summary":null,"start":131104847,"end":131353709,"strand":1,"description":"pleckstrin homology domain containing B2 [Source:HGNC Symbol;Acc:HGNC:19236]"}, {"versioned_ensembl_gene_id":"ENSG00000220884.2","gene_symbol":"MESTP1","gene_name":"mesoderm specific transcript pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338470","summary":null,"start":128928995,"end":128929988,"strand":-1,"description":"mesoderm specific transcript pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29660]"}, {"versioned_ensembl_gene_id":"ENSG00000226393.1","gene_symbol":"IFNA20P","gene_name":"interferon alpha 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:5444]","synonyms":"IFNP20","biotype":"unprocessed_pseudogene","ncbi_id":"3463","summary":null,"start":21321300,"end":21321827,"strand":1,"description":"interferon alpha 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:5444]"}, {"versioned_ensembl_gene_id":"ENSG00000254739.1","gene_symbol":"AC137894.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":528907,"end":529659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147873.5","gene_symbol":"IFNA5","gene_name":"interferon alpha 5 [Source:HGNC Symbol;Acc:HGNC:5426]","synonyms":"IFN-alphaG","biotype":"protein_coding","ncbi_id":"3442","summary":null,"start":21304326,"end":21305312,"strand":-1,"description":"interferon alpha 5 [Source:HGNC Symbol;Acc:HGNC:5426]"}, {"versioned_ensembl_gene_id":"ENSG00000274849.1","gene_symbol":"AC023043.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":36189824,"end":36190272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247708.7","gene_symbol":"STX18-AS1","gene_name":"STX18 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48877]","synonyms":"LOC100507266","biotype":"antisense_RNA","ncbi_id":"100507266","summary":null,"start":4542131,"end":4710938,"strand":1,"description":"STX18 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48877]"}, {"versioned_ensembl_gene_id":"ENSG00000234078.10","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"CD167,NEP,PTK3A,CAK,EDDR1,NTRK4,RTK6","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30925624,"end":30944801,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000226634.6","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31714445,"end":31718024,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000216306.3","gene_symbol":"KRT19P2","gene_name":"keratin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33423]","synonyms":"KRT19P5","biotype":"transcribed_processed_pseudogene","ncbi_id":"160313","summary":null,"start":94834147,"end":94835158,"strand":1,"description":"keratin 19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33423]"}, {"versioned_ensembl_gene_id":"ENSG00000280036.1","gene_symbol":"AC020661.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":41016990,"end":41018843,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088305.18","gene_symbol":"DNMT3B","gene_name":"DNA methyltransferase 3 beta [Source:HGNC Symbol;Acc:HGNC:2979]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1789","summary":"CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011]","start":32762385,"end":32809356,"strand":1,"description":"DNA methyltransferase 3 beta [Source:HGNC Symbol;Acc:HGNC:2979]"}, {"versioned_ensembl_gene_id":"ENSG00000231780.1","gene_symbol":"AC090960.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17333126,"end":17333431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213383.2","gene_symbol":"AC104297.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17871729,"end":17872598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175305.17","gene_symbol":"CCNE2","gene_name":"cyclin E2 [Source:HGNC Symbol;Acc:HGNC:1590]","synonyms":"CYCE2","biotype":"protein_coding","ncbi_id":"9134","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK2. This cyclin has been shown to specifically interact with CIP/KIP family of CDK inhibitors, and plays a role in cell cycle G1/S transition. The expression of this gene peaks at the G1-S phase and exhibits a pattern of tissue specificity distinct from that of cyclin E1. A significantly increased expression level of this gene was observed in tumor-derived cells. [provided by RefSeq, Jul 2008]","start":94879770,"end":94896678,"strand":-1,"description":"cyclin E2 [Source:HGNC Symbol;Acc:HGNC:1590]"}, {"versioned_ensembl_gene_id":"ENSG00000261154.1","gene_symbol":"LINC02131","gene_name":"long intergenic non-protein coding RNA 2131 [Source:HGNC Symbol;Acc:HGNC:52991]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371350","summary":null,"start":77590806,"end":77610681,"strand":1,"description":"long intergenic non-protein coding RNA 2131 [Source:HGNC Symbol;Acc:HGNC:52991]"}, {"versioned_ensembl_gene_id":"ENSG00000237606.2","gene_symbol":"AC091286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":104826336,"end":104826796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197258.5","gene_symbol":"EIF4BP6","gene_name":"eukaryotic translation initiation factor 4B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37939]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645579","summary":null,"start":104667749,"end":104669576,"strand":1,"description":"eukaryotic translation initiation factor 4B pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37939]"}, {"versioned_ensembl_gene_id":"ENSG00000277310.1","gene_symbol":"AC090246.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50256036,"end":50256461,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153446.15","gene_symbol":"C16orf89","gene_name":"chromosome 16 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:28687]","synonyms":"MGC45438","biotype":"protein_coding","ncbi_id":"146556","summary":"This gene is expressed predominantly in the thyroid. Based on expression patterns similar to thyroid transcription factors and proteins, this gene may function in the development and function of the thyroid. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":5044122,"end":5066110,"strand":-1,"description":"chromosome 16 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:28687]"}, {"versioned_ensembl_gene_id":"ENSG00000166444.18","gene_symbol":"ST5","gene_name":"suppression of tumorigenicity 5 [Source:HGNC Symbol;Acc:HGNC:11350]","synonyms":"p126,HTS1,DENND2B","biotype":"protein_coding","ncbi_id":"6764","summary":"This gene was identified by its ability to suppress the tumorigenicity of Hela cells in nude mice. The protein encoded by this gene contains a C-terminal region that shares similarity with the Rab 3 family of small GTP binding proteins. This protein preferentially binds to the SH3 domain of c-Abl kinase, and acts as a regulator of MAPK1/ERK2 kinase, which may contribute to its ability to reduce the tumorigenic phenotype in cells. Three alternatively spliced transcript variants of this gene encoding distinct isoforms are identified. [provided by RefSeq, Jul 2008]","start":8693351,"end":8910951,"strand":-1,"description":"suppression of tumorigenicity 5 [Source:HGNC Symbol;Acc:HGNC:11350]"}, {"versioned_ensembl_gene_id":"ENSG00000169059.12","gene_symbol":"VCX3A","gene_name":"variable charge, X-linked 3A [Source:HGNC Symbol;Acc:HGNC:18159]","synonyms":"VCX-A,VCX-8r,VCX3","biotype":"protein_coding","ncbi_id":"51481","summary":"This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. The X-linked members are clustered on chromosome Xp22 and Y-linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. VCX/Y genes encode small and highly charged proteins of unknown function. The presence of a putative bipartite nuclear localization signal suggests that VCX/Y members are nuclear proteins. This gene contains 8 repeats of the 30-bp unit. [provided by RefSeq, Jul 2008]","start":6533618,"end":6535118,"strand":-1,"description":"variable charge, X-linked 3A [Source:HGNC Symbol;Acc:HGNC:18159]"}, {"versioned_ensembl_gene_id":"ENSG00000279587.1","gene_symbol":"AC006963.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":117894632,"end":117895683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204859.12","gene_symbol":"ZBTB48","gene_name":"zinc finger and BTB domain containing 48 [Source:HGNC Symbol;Acc:HGNC:4930]","synonyms":"ZNF855,TZAP,HKR3","biotype":"protein_coding","ncbi_id":"3104","summary":null,"start":6580001,"end":6589280,"strand":1,"description":"zinc finger and BTB domain containing 48 [Source:HGNC Symbol;Acc:HGNC:4930]"}, {"versioned_ensembl_gene_id":"ENSG00000229250.1","gene_symbol":"USP9YP31","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:38775]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478930","summary":null,"start":24081704,"end":24090346,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:38775]"}, {"versioned_ensembl_gene_id":"ENSG00000185340.15","gene_symbol":"GAS2L1","gene_name":"growth arrest specific 2 like 1 [Source:HGNC Symbol;Acc:HGNC:16955]","synonyms":"GAR22","biotype":"protein_coding","ncbi_id":"10634","summary":"This gene encodes a member of the growth arrest-specific 2 protein family. This protein binds components of the cytoskeleton and may be involved in mediating interactions between microtubules and microfilaments. This protein localizes to the proximal end of mature centrioles and links centrosomes to both microtubules and actin. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 9. [provided by RefSeq, May 2018]","start":29306582,"end":29312785,"strand":1,"description":"growth arrest specific 2 like 1 [Source:HGNC Symbol;Acc:HGNC:16955]"}, {"versioned_ensembl_gene_id":"ENSG00000276446.1","gene_symbol":"AL731567.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45460633,"end":45469184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213526.3","gene_symbol":"SETP8","gene_name":"SET pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42927]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128536","summary":null,"start":116963049,"end":116963676,"strand":1,"description":"SET pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42927]"}, {"versioned_ensembl_gene_id":"ENSG00000233917.8","gene_symbol":"POTEB","gene_name":"POTE ankyrin domain family member B [Source:HGNC Symbol;Acc:HGNC:33734]","synonyms":"POTE15,POTE-15,CT104.5,A26B1","biotype":"protein_coding","ncbi_id":"100996331","summary":null,"start":21846329,"end":21877703,"strand":-1,"description":"POTE ankyrin domain family member B [Source:HGNC Symbol;Acc:HGNC:33734]"}, {"versioned_ensembl_gene_id":"ENSG00000075035.9","gene_symbol":"WSCD2","gene_name":"WSC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29117]","synonyms":"KIAA0789","biotype":"protein_coding","ncbi_id":"9671","summary":null,"start":108129471,"end":108250537,"strand":1,"description":"WSC domain containing 2 [Source:HGNC Symbol;Acc:HGNC:29117]"}, {"versioned_ensembl_gene_id":"ENSG00000230159.1","gene_symbol":"BX119904.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116692910,"end":116694188,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274275.1","gene_symbol":"AC009831.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32031035,"end":32031359,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233785.1","gene_symbol":"AC131011.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23772992,"end":23782956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279491.1","gene_symbol":"AP003733.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61967794,"end":61969490,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071889.16","gene_symbol":"FAM3A","gene_name":"family with sequence similarity 3 member A [Source:HGNC Symbol;Acc:HGNC:13749]","synonyms":"XAP-7,DXS560S,2-19","biotype":"protein_coding","ncbi_id":"60343","summary":"This gene encodes a cytokine-like protein. The expression of this gene may be regulated by peroxisome proliferator-activated receptor gamma, and the encoded protein may be involved in the regulation of glucose and lipid metabolism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":154506159,"end":154516242,"strand":-1,"description":"family with sequence similarity 3 member A [Source:HGNC Symbol;Acc:HGNC:13749]"}, {"versioned_ensembl_gene_id":"ENSG00000261056.2","gene_symbol":"AC079416.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":53298224,"end":53299792,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279795.1","gene_symbol":"AC138907.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32787962,"end":32788944,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278950.1","gene_symbol":"AC138907.8","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32781883,"end":32784138,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220891.1","gene_symbol":"LL22NC03-63E9.3","gene_name":"uncharacterized LOC648691 [Source:NCBI gene;Acc:648691]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"648691","summary":null,"start":22559343,"end":22566602,"strand":1,"description":"uncharacterized LOC648691 [Source:NCBI gene;Acc:648691]"}, {"versioned_ensembl_gene_id":"ENSG00000183632.14","gene_symbol":"TP53TG3","gene_name":"TP53 target 3 [Source:HGNC Symbol;Acc:HGNC:30759]","synonyms":"TP53TG3A,P53TG3","biotype":"protein_coding","ncbi_id":"24150","summary":null,"start":32673528,"end":32676732,"strand":-1,"description":"TP53 target 3 [Source:HGNC Symbol;Acc:HGNC:30759]"}, {"versioned_ensembl_gene_id":"ENSG00000084754.10","gene_symbol":"HADHA","gene_name":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit [Source:HGNC Symbol;Acc:HGNC:4801]","synonyms":"MTPA,LCHAD,LCEH,GBP","biotype":"protein_coding","ncbi_id":"3030","summary":"This gene encodes the alpha subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the alpha subunit catalyzing the 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase activities. Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. [provided by RefSeq, Jul 2008]","start":26190635,"end":26244726,"strand":-1,"description":"hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit [Source:HGNC Symbol;Acc:HGNC:4801]"}, {"versioned_ensembl_gene_id":"ENSG00000237874.2","gene_symbol":"AL136972.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83728055,"end":83736525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274254.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724478,"end":54736626,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000273432.1","gene_symbol":"AC004951.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":43951910,"end":44019151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279237.1","gene_symbol":"AL161773.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":110265251,"end":110266113,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225240.1","gene_symbol":"AC117490.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":196452996,"end":196453055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224090.1","gene_symbol":"AC097468.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219002215,"end":219015721,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281651.1","gene_symbol":"AC210433.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63449173,"end":63450451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278271.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789822,"end":54800920,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000234081.1","gene_symbol":"ELOCP10","gene_name":"elongin C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38146]","synonyms":"TCEB1P10","biotype":"processed_pseudogene","ncbi_id":"100462871","summary":null,"start":24006911,"end":24007237,"strand":-1,"description":"elongin C pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:38146]"}, {"versioned_ensembl_gene_id":"ENSG00000179029.14","gene_symbol":"TMEM107","gene_name":"transmembrane protein 107 [Source:HGNC Symbol;Acc:HGNC:28128]","synonyms":"MGC10744","biotype":"protein_coding","ncbi_id":"84314","summary":"This gene encodes a transmembrane protein and component of the primary cilia transition zone. The encoded protein regulates ciliogenesis and ciliary protein composition. Human fibroblasts expressing a mutant allele of this gene exhibit reduced numbers of cilia, altered cilia length, and impaired sonic hedgehog signaling. In human patients, different mutations in this gene cause different ciliopathies, including Meckel-Gruber syndrome and orofaciodigital syndrome. [provided by RefSeq, May 2017]","start":8173237,"end":8176399,"strand":-1,"description":"transmembrane protein 107 [Source:HGNC Symbol;Acc:HGNC:28128]"}, {"versioned_ensembl_gene_id":"ENSG00000224174.2","gene_symbol":"AL137802.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16520694,"end":16521796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234558.1","gene_symbol":"API5P1","gene_name":"apoptosis inhibitor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:595]","synonyms":"API5L1","biotype":"processed_pseudogene","ncbi_id":"642812","summary":null,"start":116106921,"end":116108430,"strand":-1,"description":"apoptosis inhibitor 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:595]"}, {"versioned_ensembl_gene_id":"ENSG00000227458.8","gene_symbol":"TRIM40","gene_name":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]","synonyms":"RNF35","biotype":"protein_coding","ncbi_id":"135644","summary":"This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]","start":30126433,"end":30139059,"strand":1,"description":"tripartite motif containing 40 [Source:HGNC Symbol;Acc:HGNC:18736]"}, {"versioned_ensembl_gene_id":"ENSG00000229335.1","gene_symbol":"DANT1","gene_name":"DXZ4 associated non-coding transcript 1, proximal [Source:HGNC Symbol;Acc:HGNC:50863]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"106029310","summary":null,"start":115840964,"end":115843050,"strand":1,"description":"DXZ4 associated non-coding transcript 1, proximal [Source:HGNC Symbol;Acc:HGNC:50863]"}, {"versioned_ensembl_gene_id":"ENSG00000275336.1","gene_symbol":"AL355493.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":27378657,"end":27388552,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282226.1","gene_symbol":"AC093614.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135676,"end":149167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152779.13","gene_symbol":"SLC16A12","gene_name":"solute carrier family 16 member 12 [Source:HGNC Symbol;Acc:HGNC:23094]","synonyms":"MCT12","biotype":"protein_coding","ncbi_id":"387700","summary":"This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]","start":89430299,"end":89556641,"strand":-1,"description":"solute carrier family 16 member 12 [Source:HGNC Symbol;Acc:HGNC:23094]"}, {"versioned_ensembl_gene_id":"ENSG00000203593.3","gene_symbol":"AC005342.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2004666,"end":2011392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274840.4","gene_symbol":"AC132807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18013226,"end":18041603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274952.5","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"nkat2b,p58,CD158B2,cl-6,nkat2,nkat2a","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54669793,"end":54684345,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000262535.5","gene_symbol":"OR5G5P","gene_name":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"81191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56812930,"end":56831496,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 5 pseudogene [Source:HGNC Symbol;Acc:HGNC:15289]"}, {"versioned_ensembl_gene_id":"ENSG00000281107.1","gene_symbol":"OR5G3","gene_name":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]","synonyms":"OR5G3P,OR5G6P","biotype":"polymorphic_pseudogene","ncbi_id":"81193","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":56830655,"end":56831590,"strand":-1,"description":"olfactory receptor family 5 subfamily G member 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15287]"}, {"versioned_ensembl_gene_id":"ENSG00000260994.1","gene_symbol":"AGGF1P7","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51740]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132606","summary":null,"start":35547917,"end":35548829,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:51740]"}, {"versioned_ensembl_gene_id":"ENSG00000259996.1","gene_symbol":"RARRES2P8","gene_name":"retinoic acid receptor responder 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48707]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642652","summary":null,"start":35543279,"end":35543645,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:48707]"}, {"versioned_ensembl_gene_id":"ENSG00000260857.2","gene_symbol":"AC018558.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35505093,"end":35506462,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250710.3","gene_symbol":"OR7E99P","gene_name":"olfactory receptor family 7 subfamily E member 99 pseudogene [Source:HGNC Symbol;Acc:HGNC:15059]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81419","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4156522,"end":4157443,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 99 pseudogene [Source:HGNC Symbol;Acc:HGNC:15059]"}, {"versioned_ensembl_gene_id":"ENSG00000284734.1","gene_symbol":"AC099063.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89198714,"end":89207040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230674.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29526002,"end":29530150,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000213450.4","gene_symbol":"VDAC1P7","gene_name":"voltage dependent anion channel 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37482]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100310839","summary":null,"start":77316752,"end":77317598,"strand":-1,"description":"voltage dependent anion channel 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37482]"}, {"versioned_ensembl_gene_id":"ENSG00000166707.10","gene_symbol":"ZCCHC18","gene_name":"zinc finger CCHC-type containing 18 [Source:HGNC Symbol;Acc:HGNC:32459]","synonyms":"SIZN2,PNMA7B","biotype":"protein_coding","ncbi_id":"644353","summary":null,"start":104112131,"end":104115846,"strand":1,"description":"zinc finger CCHC-type containing 18 [Source:HGNC Symbol;Acc:HGNC:32459]"}, {"versioned_ensembl_gene_id":"ENSG00000250672.1","gene_symbol":"AC010343.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33090126,"end":33090349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249102.1","gene_symbol":"AC034223.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33008994,"end":33025724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213068.3","gene_symbol":"AL451050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":167162423,"end":167162837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256417.1","gene_symbol":"AC006206.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5290480,"end":5383653,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226403.1","gene_symbol":"AL392089.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":547317,"end":549531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235330.2","gene_symbol":"RPL12P25","gene_name":"ribosomal protein L12 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37008]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100270926","summary":null,"start":477750,"end":478423,"strand":1,"description":"ribosomal protein L12 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:37008]"}, {"versioned_ensembl_gene_id":"ENSG00000243071.1","gene_symbol":"AC107032.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76660405,"end":76660884,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257904.1","gene_symbol":"AL133372.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29940745,"end":29980212,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226238.1","gene_symbol":"AC132807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17990023,"end":17995544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233776.5","gene_symbol":"LINC01251","gene_name":"long intergenic non-protein coding RNA 1251 [Source:HGNC Symbol;Acc:HGNC:49845]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101929688","summary":null,"start":33732975,"end":33738416,"strand":-1,"description":"long intergenic non-protein coding RNA 1251 [Source:HGNC Symbol;Acc:HGNC:49845]"}, {"versioned_ensembl_gene_id":"ENSG00000134444.13","gene_symbol":"KIAA1468","gene_name":"KIAA1468 [Source:HGNC Symbol;Acc:HGNC:29289]","synonyms":"HsT3308,FLJ33841,HsT885","biotype":"protein_coding","ncbi_id":"57614","summary":null,"start":62187258,"end":62307829,"strand":1,"description":"KIAA1468 [Source:HGNC Symbol;Acc:HGNC:29289]"}, {"versioned_ensembl_gene_id":"ENSG00000251357.4","gene_symbol":"AP000350.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23862188,"end":23895223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123080.10","gene_symbol":"CDKN2C","gene_name":"cyclin dependent kinase inhibitor 2C [Source:HGNC Symbol;Acc:HGNC:1789]","synonyms":"p18,INK4C","biotype":"protein_coding","ncbi_id":"1031","summary":"The protein encoded by this gene is a member of the INK4 family of cyclin-dependent kinase inhibitors. This protein has been shown to interact with CDK4 or CDK6, and prevent the activation of the CDK kinases, thus function as a cell growth regulator that controls cell cycle G1 progression. Ectopic expression of this gene was shown to suppress the growth of human cells in a manner that appears to correlate with the presence of a wild-type RB1 function. Studies in the knockout mice suggested the roles of this gene in regulating spermatogenesis, as well as in suppressing tumorigenesis. Two alternatively spliced transcript variants of this gene, which encode an identical protein, have been reported. [provided by RefSeq, Jul 2008]","start":50960745,"end":50974633,"strand":1,"description":"cyclin dependent kinase inhibitor 2C [Source:HGNC Symbol;Acc:HGNC:1789]"}, {"versioned_ensembl_gene_id":"ENSG00000273840.1","gene_symbol":"AF254983.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":10482738,"end":10605716,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184330.11","gene_symbol":"S100A7A","gene_name":"S100 calcium binding protein A7A [Source:HGNC Symbol;Acc:HGNC:21657]","synonyms":"S100A7L1,S100A7f,S100A15","biotype":"protein_coding","ncbi_id":"338324","summary":null,"start":153416524,"end":153423225,"strand":1,"description":"S100 calcium binding protein A7A [Source:HGNC Symbol;Acc:HGNC:21657]"}, {"versioned_ensembl_gene_id":"ENSG00000271042.1","gene_symbol":"AL078603.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99082449,"end":99082761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227914.3","gene_symbol":"AL136979.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":673478,"end":685555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226313.1","gene_symbol":"MTCYBP12","gene_name":"mitochondrially encoded cytochrome b pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51963]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075123","summary":null,"start":5169512,"end":5170645,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:51963]"}, {"versioned_ensembl_gene_id":"ENSG00000134716.9","gene_symbol":"CYP2J2","gene_name":"cytochrome P450 family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:2634]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1573","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is thought to be the predominant enzyme responsible for epoxidation of endogenous arachidonic acid in cardiac tissue. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]","start":59893308,"end":59926790,"strand":-1,"description":"cytochrome P450 family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:2634]"}, {"versioned_ensembl_gene_id":"ENSG00000259511.2","gene_symbol":"UBE2Q2L","gene_name":"ubiquitin conjugating enzyme E2 Q2 like [Source:HGNC Symbol;Acc:HGNC:44656]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100505679","summary":null,"start":84172490,"end":84182234,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 like [Source:HGNC Symbol;Acc:HGNC:44656]"}, {"versioned_ensembl_gene_id":"ENSG00000232910.1","gene_symbol":"RAB9AP1","gene_name":"RAB9A, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38104]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287200","summary":null,"start":23751188,"end":23751760,"strand":1,"description":"RAB9A, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38104]"}, {"versioned_ensembl_gene_id":"ENSG00000198787.5","gene_symbol":"OR4D12P","gene_name":"olfactory receptor family 4 subfamily D member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19587]","synonyms":"OR7E103P","biotype":"unprocessed_pseudogene","ncbi_id":"282754","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":4126659,"end":4127569,"strand":-1,"description":"olfactory receptor family 4 subfamily D member 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:19587]"}, {"versioned_ensembl_gene_id":"ENSG00000122035.6","gene_symbol":"RASL11A","gene_name":"RAS like family 11 member A [Source:HGNC Symbol;Acc:HGNC:23802]","synonyms":null,"biotype":"protein_coding","ncbi_id":"387496","summary":"RASL11A is a member of the small GTPase protein family with a high degree of similarity to RAS (see HRAS, MIM 190020) proteins.[supplied by OMIM, Nov 2008]","start":27270327,"end":27273690,"strand":1,"description":"RAS like family 11 member A [Source:HGNC Symbol;Acc:HGNC:23802]"}, {"versioned_ensembl_gene_id":"ENSG00000116863.10","gene_symbol":"ADPRHL2","gene_name":"ADP-ribosylhydrolase like 2 [Source:HGNC Symbol;Acc:HGNC:21304]","synonyms":"FLJ20446,ARH3","biotype":"protein_coding","ncbi_id":"54936","summary":"This gene encodes a member of the ADP-ribosylglycohydrolase family. The encoded enzyme catalyzes the removal of ADP-ribose from ADP-ribosylated proteins. This enzyme localizes to the mitochondria, in addition to the nucleus and cytoplasm.[provided by RefSeq, Feb 2009]","start":36088875,"end":36093932,"strand":1,"description":"ADP-ribosylhydrolase like 2 [Source:HGNC Symbol;Acc:HGNC:21304]"}, {"versioned_ensembl_gene_id":"ENSG00000280354.1","gene_symbol":"AC073592.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124542503,"end":124542873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279121.1","gene_symbol":"AC073592.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124555905,"end":124556432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279639.2","gene_symbol":"AC135068.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21574225,"end":21575207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137814.10","gene_symbol":"HAUS2","gene_name":"HAUS augmin like complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:25530]","synonyms":"HsT17025,FLJ10460,CEP27,C15orf25","biotype":"protein_coding","ncbi_id":"55142","summary":"The protein encoded by this gene is a subunit of the augmin complex. The augmin complex plays a role in microtubule attachment to the kinetochore and central spindle formation. [provided by RefSeq, Apr 2016]","start":42548810,"end":42569994,"strand":1,"description":"HAUS augmin like complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:25530]"}, {"versioned_ensembl_gene_id":"ENSG00000241468.7","gene_symbol":"ATP5J2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 [Source:HGNC Symbol;Acc:HGNC:848]","synonyms":"ATP5JL","biotype":"protein_coding","ncbi_id":"9551","summary":"Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The catalytic portion of mitochondrial ATP synthase consists of five different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the f subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has multiple pseudogenes. Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene. [provided by RefSeq, Nov 2010]","start":99448475,"end":99466331,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 [Source:HGNC Symbol;Acc:HGNC:848]"}, {"versioned_ensembl_gene_id":"ENSG00000232692.1","gene_symbol":"AP001596.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26378552,"end":26471698,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278754.1","gene_symbol":"AL513423.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15524576,"end":15524707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228956.8","gene_symbol":"SATB1-AS1","gene_name":"SATB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50687]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101927777","summary":null,"start":18445024,"end":18920401,"strand":1,"description":"SATB1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50687]"}, {"versioned_ensembl_gene_id":"ENSG00000227067.3","gene_symbol":"DPPA3P1","gene_name":"developmental pluripotency associated 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32345]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728493","summary":null,"start":103961811,"end":103962279,"strand":-1,"description":"developmental pluripotency associated 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32345]"}, {"versioned_ensembl_gene_id":"ENSG00000256025.1","gene_symbol":"CACNA1C-AS4","gene_name":"CACNA1C antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40116]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874234","summary":null,"start":2220537,"end":2223479,"strand":-1,"description":"CACNA1C antisense RNA 4 [Source:HGNC Symbol;Acc:HGNC:40116]"}, {"versioned_ensembl_gene_id":"ENSG00000217130.1","gene_symbol":"AL139100.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34744176,"end":34744673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236570.1","gene_symbol":"RAD23BP1","gene_name":"RAD23 homolog B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44509]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"131185","summary":null,"start":18538673,"end":18539899,"strand":1,"description":"RAD23 homolog B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44509]"}, {"versioned_ensembl_gene_id":"ENSG00000271021.1","gene_symbol":"AC239600.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115454733,"end":115455194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274374.1","gene_symbol":"AC239600.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115424064,"end":115425600,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140527.14","gene_symbol":"WDR93","gene_name":"WD repeat domain 93 [Source:HGNC Symbol;Acc:HGNC:26924]","synonyms":null,"biotype":"protein_coding","ncbi_id":"56964","summary":null,"start":89690797,"end":89743638,"strand":1,"description":"WD repeat domain 93 [Source:HGNC Symbol;Acc:HGNC:26924]"}, {"versioned_ensembl_gene_id":"ENSG00000197934.8","gene_symbol":"CYYR1-AS1","gene_name":"cysteine and tyrosine rich 1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39560]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996571","summary":null,"start":26393635,"end":26569252,"strand":1,"description":"cysteine and tyrosine rich 1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39560]"}, {"versioned_ensembl_gene_id":"ENSG00000259561.1","gene_symbol":"AC079075.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":89704665,"end":89705415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250609.1","gene_symbol":"AC110753.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154523487,"end":154524807,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272457.1","gene_symbol":"AC113194.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53876150,"end":53876649,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273045.5","gene_symbol":"C2orf15","gene_name":"chromosome 2 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:28436]","synonyms":"MGC29762","biotype":"protein_coding","ncbi_id":"150590","summary":null,"start":99141485,"end":99151487,"strand":1,"description":"chromosome 2 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:28436]"}, {"versioned_ensembl_gene_id":"ENSG00000269293.2","gene_symbol":"ZSCAN16-AS1","gene_name":"ZSCAN16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48982]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129195","summary":null,"start":28121795,"end":28137293,"strand":-1,"description":"ZSCAN16 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48982]"}, {"versioned_ensembl_gene_id":"ENSG00000261839.1","gene_symbol":"AL358933.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28136849,"end":28139678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115524.15","gene_symbol":"SF3B1","gene_name":"splicing factor 3b subunit 1 [Source:HGNC Symbol;Acc:HGNC:10768]","synonyms":"SF3b155,SAP155,PRPF10,Prp10,Hsh155","biotype":"protein_coding","ncbi_id":"23451","summary":"This gene encodes subunit 1 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence independent manner and may anchor the U2 snRNP to the pre-mRNA. Splicing factor 3b is also a component of the minor U12-type spliceosome. The carboxy-terminal two-thirds of subunit 1 have 22 non-identical, tandem HEAT repeats that form rod-like, helical structures. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":197389784,"end":197435091,"strand":-1,"description":"splicing factor 3b subunit 1 [Source:HGNC Symbol;Acc:HGNC:10768]"}, {"versioned_ensembl_gene_id":"ENSG00000279366.1","gene_symbol":"AC120349.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47912207,"end":47912504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214581.6","gene_symbol":"ZNF971P","gene_name":"zinc finger protein 971, pseudogene [Source:HGNC Symbol;Acc:HGNC:51848]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100419895","summary":null,"start":35446898,"end":35449411,"strand":-1,"description":"zinc finger protein 971, pseudogene [Source:HGNC Symbol;Acc:HGNC:51848]"}, {"versioned_ensembl_gene_id":"ENSG00000133619.17","gene_symbol":"KRBA1","gene_name":"KRAB-A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22228]","synonyms":"KIAA1862","biotype":"protein_coding","ncbi_id":"84626","summary":null,"start":149714781,"end":149734575,"strand":1,"description":"KRAB-A domain containing 1 [Source:HGNC Symbol;Acc:HGNC:22228]"}, {"versioned_ensembl_gene_id":"ENSG00000277173.1","gene_symbol":"AC004241.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47768529,"end":47769648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233805.1","gene_symbol":"AL365496.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53766400,"end":53766614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238090.1","gene_symbol":"AC006195.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33379964,"end":33380886,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231399.1","gene_symbol":"SNRPEP8","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43573]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874423","summary":null,"start":53038285,"end":53038544,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43573]"}, {"versioned_ensembl_gene_id":"ENSG00000176542.9","gene_symbol":"USF3","gene_name":"upstream transcription factor family member 3 [Source:HGNC Symbol;Acc:HGNC:30494]","synonyms":"KIAA2018","biotype":"protein_coding","ncbi_id":"205717","summary":"This gene encodes a large protein that contains a helix-loop-helix domain and a polyglutamine region. A deletion in the polyglutamine region was associated with risk for thyroid carcinoma. [provided by RefSeq, May 2017]","start":113648385,"end":113696646,"strand":-1,"description":"upstream transcription factor family member 3 [Source:HGNC Symbol;Acc:HGNC:30494]"}, {"versioned_ensembl_gene_id":"ENSG00000235189.1","gene_symbol":"AL034405.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129869064,"end":129957528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260322.1","gene_symbol":"AC098657.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":80114943,"end":80116918,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240441.1","gene_symbol":"AC007622.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107719599,"end":107720133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262420.3","gene_symbol":"AC007613.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11741910,"end":11744506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227121.1","gene_symbol":"AC073174.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52973488,"end":52975815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232676.1","gene_symbol":"ADH5P2","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343296","summary":null,"start":79521080,"end":79522203,"strand":1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22976]"}, {"versioned_ensembl_gene_id":"ENSG00000169752.16","gene_symbol":"NRG4","gene_name":"neuregulin 4 [Source:HGNC Symbol;Acc:HGNC:29862]","synonyms":"HRG4","biotype":"protein_coding","ncbi_id":"145957","summary":"The neuregulins, including NRG4, activate type-1 growth factor receptors (see EGFR; MIM 131550) to initiating cell-to-cell signaling through tyrosine phosphorylation (Harari et al., 1999 [PubMed 10348342]).[supplied by OMIM, Mar 2008]","start":75935969,"end":76059795,"strand":-1,"description":"neuregulin 4 [Source:HGNC Symbol;Acc:HGNC:29862]"}, {"versioned_ensembl_gene_id":"ENSG00000235011.2","gene_symbol":"AL353651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79323769,"end":79324863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282898.1","gene_symbol":"AL353651.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79323769,"end":79324852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092051.16","gene_symbol":"JPH4","gene_name":"junctophilin 4 [Source:HGNC Symbol;Acc:HGNC:20156]","synonyms":"KIAA1831,JPHL1","biotype":"protein_coding","ncbi_id":"84502","summary":"This gene encodes a member of the junctophilin family of transmembrane proteins that are involved in the formation of the junctional membrane complexes between the plasma membrane and the endoplasmic/sarcoplasmic reticulum in excitable cells. The encoded protein contains a conserved N-terminal repeat region called the membrane occupation and recognition nexus sequence that is found in other members of the junctophilin family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":23568035,"end":23578800,"strand":-1,"description":"junctophilin 4 [Source:HGNC Symbol;Acc:HGNC:20156]"}, {"versioned_ensembl_gene_id":"ENSG00000232906.1","gene_symbol":"AC092685.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":65355934,"end":65357176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256030.1","gene_symbol":"CBX3P4","gene_name":"chromobox 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42876]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100873792","summary":null,"start":2786931,"end":2794295,"strand":-1,"description":"chromobox 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42876]"}, {"versioned_ensembl_gene_id":"ENSG00000165471.6","gene_symbol":"MBL2","gene_name":"mannose binding lectin 2 [Source:HGNC Symbol;Acc:HGNC:6922]","synonyms":"MBL,COLEC1","biotype":"protein_coding","ncbi_id":"4153","summary":"This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes and binds to mannose and N-acetylglucosamine on many microorganisms, including bacteria, yeast, and viruses including influenza virus, HIV and SARS-CoV. This binding activates the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases. [provided by RefSeq, Jun 2020]","start":52765380,"end":52771700,"strand":-1,"description":"mannose binding lectin 2 [Source:HGNC Symbol;Acc:HGNC:6922]"}, {"versioned_ensembl_gene_id":"ENSG00000218537.1","gene_symbol":"MIF-AS1","gene_name":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]","synonyms":"MIF-AS,LOC284889","biotype":"antisense_RNA","ncbi_id":"284889","summary":null,"start":23894426,"end":23898930,"strand":-1,"description":"MIF antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27669]"}, {"versioned_ensembl_gene_id":"ENSG00000250885.1","gene_symbol":"LINC02061","gene_name":"long intergenic non-protein coding RNA 2061 [Source:HGNC Symbol;Acc:HGNC:52906]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374714","summary":null,"start":32646564,"end":32651976,"strand":-1,"description":"long intergenic non-protein coding RNA 2061 [Source:HGNC Symbol;Acc:HGNC:52906]"}, {"versioned_ensembl_gene_id":"ENSG00000270874.1","gene_symbol":"RPAP2P1","gene_name":"RNA polymerase II associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45125]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100272220","summary":null,"start":86854696,"end":86856236,"strand":-1,"description":"RNA polymerase II associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45125]"}, {"versioned_ensembl_gene_id":"ENSG00000214595.11","gene_symbol":"EML6","gene_name":"echinoderm microtubule associated protein like 6 [Source:HGNC Symbol;Acc:HGNC:35412]","synonyms":"FLJ42562","biotype":"protein_coding","ncbi_id":"400954","summary":null,"start":54723499,"end":54972025,"strand":1,"description":"echinoderm microtubule associated protein like 6 [Source:HGNC Symbol;Acc:HGNC:35412]"}, {"versioned_ensembl_gene_id":"ENSG00000174876.16","gene_symbol":"AMY1B","gene_name":"amylase, alpha 1B (salivary) [Source:HGNC Symbol;Acc:HGNC:475]","synonyms":"AMY1","biotype":"protein_coding","ncbi_id":"277","summary":"Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen. The human genome has a cluster of several amylase genes that are expressed at high levels in either salivary gland or pancreas. This gene encodes an amylase isoenzyme produced by the salivary gland. [provided by RefSeq, Jul 2008]","start":103687415,"end":103696680,"strand":-1,"description":"amylase, alpha 1B (salivary) [Source:HGNC Symbol;Acc:HGNC:475]"}, {"versioned_ensembl_gene_id":"ENSG00000158815.10","gene_symbol":"FGF17","gene_name":"fibroblast growth factor 17 [Source:HGNC Symbol;Acc:HGNC:3673]","synonyms":"FGF-13","biotype":"protein_coding","ncbi_id":"8822","summary":"This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":22042398,"end":22048809,"strand":1,"description":"fibroblast growth factor 17 [Source:HGNC Symbol;Acc:HGNC:3673]"}, {"versioned_ensembl_gene_id":"ENSG00000106605.10","gene_symbol":"BLVRA","gene_name":"biliverdin reductase A [Source:HGNC Symbol;Acc:HGNC:1062]","synonyms":"BLVR","biotype":"protein_coding","ncbi_id":"644","summary":"The protein encoded by this gene belongs to the biliverdin reductase family, members of which catalyze the conversion of biliverdin to bilirubin in the presence of NADPH or NADH. Mutations in this gene are associated with hyperbiliverdinemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2011]","start":43758680,"end":43807342,"strand":1,"description":"biliverdin reductase A [Source:HGNC Symbol;Acc:HGNC:1062]"}, {"versioned_ensembl_gene_id":"ENSG00000116032.5","gene_symbol":"GRIN3B","gene_name":"glutamate ionotropic receptor NMDA type subunit 3B [Source:HGNC Symbol;Acc:HGNC:16768]","synonyms":"GluN3B","biotype":"protein_coding","ncbi_id":"116444","summary":"The protein encoded by this gene is a subunit of an N-methyl-D-aspartate (NMDA) receptor. The encoded protein is found primarily in motor neurons, where it forms a heterotetramer with GRIN1 to create an excitatory glycine receptor. Variations in this gene have been proposed to be linked to schizophrenia. [provided by RefSeq, Nov 2015]","start":1000419,"end":1009732,"strand":1,"description":"glutamate ionotropic receptor NMDA type subunit 3B [Source:HGNC Symbol;Acc:HGNC:16768]"}, {"versioned_ensembl_gene_id":"ENSG00000168267.6","gene_symbol":"PTF1A","gene_name":"pancreas specific transcription factor, 1a [Source:HGNC Symbol;Acc:HGNC:23734]","synonyms":"PTF1-p48,bHLHa29","biotype":"protein_coding","ncbi_id":"256297","summary":"This gene encodes a protein that is a component of the pancreas transcription factor 1 complex (PTF1) and is known to have a role in mammalian pancreatic development. The protein plays a role in determining whether cells allocated to the pancreatic buds continue towards pancreatic organogenesis or revert back to duodenal fates. The protein is thought to be involved in the maintenance of exocrine pancreas-specific gene expression including elastase 1 and amylase. Mutations in this gene cause cerebellar agenesis and loss of expression is seen in ductal type pancreas cancers. [provided by RefSeq, Jul 2008]","start":23192327,"end":23194252,"strand":1,"description":"pancreas specific transcription factor, 1a [Source:HGNC Symbol;Acc:HGNC:23734]"}, {"versioned_ensembl_gene_id":"ENSG00000163467.11","gene_symbol":"TSACC","gene_name":"TSSK6 activating cochaperone [Source:HGNC Symbol;Acc:HGNC:30636]","synonyms":"SSTK-IP,SIP,C1orf182","biotype":"protein_coding","ncbi_id":"128229","summary":null,"start":156337314,"end":156346995,"strand":1,"description":"TSSK6 activating cochaperone [Source:HGNC Symbol;Acc:HGNC:30636]"}, {"versioned_ensembl_gene_id":"ENSG00000205078.5","gene_symbol":"SYCE1L","gene_name":"synaptonemal complex central element protein 1 like [Source:HGNC Symbol;Acc:HGNC:37236]","synonyms":"MRP2","biotype":"protein_coding","ncbi_id":"100130958","summary":null,"start":77199397,"end":77213215,"strand":1,"description":"synaptonemal complex central element protein 1 like [Source:HGNC Symbol;Acc:HGNC:37236]"}, {"versioned_ensembl_gene_id":"ENSG00000165131.6","gene_symbol":"C7orf34","gene_name":"chromosome 7 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:21750]","synonyms":"CTM-1","biotype":"protein_coding","ncbi_id":"135927","summary":null,"start":142939343,"end":142940868,"strand":1,"description":"chromosome 7 open reading frame 34 [Source:HGNC Symbol;Acc:HGNC:21750]"}, {"versioned_ensembl_gene_id":"ENSG00000243508.1","gene_symbol":"AC108688.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":125344085,"end":125344797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102001.12","gene_symbol":"CACNA1F","gene_name":"calcium voltage-gated channel subunit alpha1 F [Source:HGNC Symbol;Acc:HGNC:1393]","synonyms":"OA2,JMC8,JM8,CSNBX2,CSNB2,CSNB2A,CORDX3,Cav1.4,AIED","biotype":"protein_coding","ncbi_id":"778","summary":"This gene encodes a multipass transmembrane protein that functions as an alpha-1 subunit of the voltage-dependent calcium channel, which mediates the influx of calcium ions into the cell. The encoded protein forms a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Mutations in this gene can cause X-linked eye disorders, including congenital stationary night blindness type 2A, cone-rod dystropy, and Aland Island eye disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2013]","start":49205063,"end":49233371,"strand":-1,"description":"calcium voltage-gated channel subunit alpha1 F [Source:HGNC Symbol;Acc:HGNC:1393]"}, {"versioned_ensembl_gene_id":"ENSG00000272319.2","gene_symbol":"AL022345.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42579724,"end":42579858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232713.2","gene_symbol":"AC010733.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60938204,"end":60938604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197603.13","gene_symbol":"C5orf42","gene_name":"chromosome 5 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:25801]","synonyms":"JBTS17,Hug,FLJ13231","biotype":"protein_coding","ncbi_id":"65250","summary":"The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]","start":37106228,"end":37249428,"strand":-1,"description":"chromosome 5 open reading frame 42 [Source:HGNC Symbol;Acc:HGNC:25801]"}, {"versioned_ensembl_gene_id":"ENSG00000284523.1","gene_symbol":"AC004834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99252452,"end":99325826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235432.1","gene_symbol":"AL663074.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":20692734,"end":20694013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067334.13","gene_symbol":"DNTTIP2","gene_name":"deoxynucleotidyltransferase terminal interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:24013]","synonyms":"TdIF2,HSU15552,ERBP","biotype":"protein_coding","ncbi_id":"30836","summary":"This gene is thought to be involved in chromatin remodeling and gene transcription. The encoded nuclear protein binds to and enhances the transcriptional activity of the estrogen receptor alpha, and also interacts with terminal deoxynucleotidyltransferase. The expression profile of this gene is a potential biomarker for chronic obstructive pulmonary disease. [provided by RefSeq, Dec 2010]","start":93866283,"end":93879918,"strand":-1,"description":"deoxynucleotidyltransferase terminal interacting protein 2 [Source:HGNC Symbol;Acc:HGNC:24013]"}, {"versioned_ensembl_gene_id":"ENSG00000229428.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29923540,"end":29923724,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000260464.1","gene_symbol":"AL049796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93847174,"end":93848939,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257114.2","gene_symbol":"LINC02450","gene_name":"long intergenic non-protein coding RNA 2450 [Source:HGNC Symbol;Acc:HGNC:53382]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369739","summary":null,"start":42692216,"end":42717119,"strand":1,"description":"long intergenic non-protein coding RNA 2450 [Source:HGNC Symbol;Acc:HGNC:53382]"}, {"versioned_ensembl_gene_id":"ENSG00000133624.13","gene_symbol":"ZNF767P","gene_name":"zinc finger family member 767, pseudogene [Source:HGNC Symbol;Acc:HGNC:21884]","synonyms":"ZNF767,FLJ12700","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"79970","summary":null,"start":149547154,"end":149624752,"strand":-1,"description":"zinc finger family member 767, pseudogene [Source:HGNC Symbol;Acc:HGNC:21884]"}, {"versioned_ensembl_gene_id":"ENSG00000271980.1","gene_symbol":"AC012640.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10264597,"end":10267146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257046.5","gene_symbol":"AC011604.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":20815674,"end":21090245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282247.1","gene_symbol":"AC245049.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15351236,"end":15351605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271332.1","gene_symbol":"AC023206.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28144907,"end":28145204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072858.10","gene_symbol":"SIDT1","gene_name":"SID1 transmembrane family member 1 [Source:HGNC Symbol;Acc:HGNC:25967]","synonyms":"SID-1,FLJ20174","biotype":"protein_coding","ncbi_id":"54847","summary":"The protein encoded by this gene belongs to SID1 family of transmembrane dsRNA-gated channels. Family members transport dsRNA into cells and are required for systemic RNA interference. [provided by RefSeq, May 2017]","start":113532296,"end":113629578,"strand":1,"description":"SID1 transmembrane family member 1 [Source:HGNC Symbol;Acc:HGNC:25967]"}, {"versioned_ensembl_gene_id":"ENSG00000275826.1","gene_symbol":"AC093909.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188713644,"end":188715442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168131.4","gene_symbol":"OR2B2","gene_name":"olfactory receptor family 2 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:13966]","synonyms":"OR6-1,OR2B9,OR2B2Q,hs6M1-10","biotype":"protein_coding","ncbi_id":"81697","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":27911185,"end":27912396,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 2 [Source:HGNC Symbol;Acc:HGNC:13966]"}, {"versioned_ensembl_gene_id":"ENSG00000181773.6","gene_symbol":"GPR3","gene_name":"G protein-coupled receptor 3 [Source:HGNC Symbol;Acc:HGNC:4484]","synonyms":"ACCA","biotype":"protein_coding","ncbi_id":"2827","summary":"This gene is a member of the G protein-coupled receptor family and is found in the cell membrane. G protein-coupled receptors, characterized by a seven transmembrane domain motif, are involved in translating outside signals into G protein mediated intracellular effects. The encoded protein activates adenylate cyclase and modulates amyloid-beta production in a mouse model, suggesting that it may play a role in Alzheimer's disease. [provided by RefSeq, Oct 2012]","start":27392644,"end":27395814,"strand":1,"description":"G protein-coupled receptor 3 [Source:HGNC Symbol;Acc:HGNC:4484]"}, {"versioned_ensembl_gene_id":"ENSG00000229035.2","gene_symbol":"SPRR2C","gene_name":"small proline rich protein 2C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11263]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"6702","summary":null,"start":153140491,"end":153140709,"strand":-1,"description":"small proline rich protein 2C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:11263]"}, {"versioned_ensembl_gene_id":"ENSG00000188897.8","gene_symbol":"AC099489.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":11359845,"end":11523588,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283459.1","gene_symbol":"AC009804.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114894632,"end":114898529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260975.1","gene_symbol":"AC007333.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52198012,"end":52227956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278195.1","gene_symbol":"SSTR3","gene_name":"somatostatin receptor 3 [Source:HGNC Symbol;Acc:HGNC:11332]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6753","summary":"This gene encodes a member of the somatostatin receptor protein family. Somatostatins are peptide hormones that regulate diverse cellular functions such as neurotransmission, cell proliferation, and endocrine signaling as well as inhibiting the release of many hormones and other secretory proteins. Somatostatin has two active forms of 14 and 28 amino acids. The biological effects of somatostatins are mediated by a family of G-protein coupled somatostatin receptors that are expressed in a tissue-specific manner. Somatostatin receptors form homodimers and heterodimers with other members of the superfamily as well as with other G-protein coupled receptors and receptor tyrosine kinases. This protein is functionally coupled to adenylyl cyclase. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":37204238,"end":37212322,"strand":-1,"description":"somatostatin receptor 3 [Source:HGNC Symbol;Acc:HGNC:11332]"}, {"versioned_ensembl_gene_id":"ENSG00000261749.2","gene_symbol":"LINC02180","gene_name":"long intergenic non-protein coding RNA 2180 [Source:HGNC Symbol;Acc:HGNC:53042]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102467079","summary":null,"start":52085280,"end":52099067,"strand":1,"description":"long intergenic non-protein coding RNA 2180 [Source:HGNC Symbol;Acc:HGNC:53042]"}, {"versioned_ensembl_gene_id":"ENSG00000263620.1","gene_symbol":"AC129492.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":8150816,"end":8162975,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232118.2","gene_symbol":"BACH1-AS1","gene_name":"BACH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40008]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106478962","summary":null,"start":29370019,"end":29376339,"strand":-1,"description":"BACH1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40008]"}, {"versioned_ensembl_gene_id":"ENSG00000099797.13","gene_symbol":"TECR","gene_name":"trans-2,3-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:4551]","synonyms":"SC2,MRT14,GPSN2,TER","biotype":"protein_coding","ncbi_id":"9524","summary":"This gene encodes a multi-pass membrane protein that resides in the endoplasmic reticulum, and belongs to the steroid 5-alpha reductase family. The elongation of microsomal long and very long chain fatty acid consists of 4 sequential reactions. This protein catalyzes the final step, reducing trans-2,3-enoyl-CoA to saturated acyl-CoA. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Apr 2011]","start":14517085,"end":14565980,"strand":1,"description":"trans-2,3-enoyl-CoA reductase [Source:HGNC Symbol;Acc:HGNC:4551]"}, {"versioned_ensembl_gene_id":"ENSG00000279253.1","gene_symbol":"AL121753.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35262727,"end":35264187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162430.16","gene_symbol":"SELENON","gene_name":"selenoprotein N [Source:HGNC Symbol;Acc:HGNC:15999]","synonyms":"RSS,RSMD1,MDRS1,SEPN1,SELN","biotype":"protein_coding","ncbi_id":"57190","summary":"This gene encodes a glycoprotein that is localized in the endoplasmic reticulum. It plays an important role in cell protection against oxidative stress, and in the regulation of redox-related calcium homeostasis. Mutations in this gene are associated with early onset muscle disorders, referred to as SEPN1-related myopathy. SEPN1-related myopathy consists of 4 autosomal recessive disorders, originally thought to be separate entities: rigid spine muscular dystrophy (RSMD1), the classical form of multiminicore disease, desmin related myopathy with Mallory-body like inclusions, and congenital fiber-type disproportion (CFTD). This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. A second stop-codon redefinition element (SRE) adjacent to the UGA codon has been identified in this gene (PMID:15791204). SRE is a phylogenetically conserved stem-loop structure that stimulates readthrough at the UGA codon, and augments the Sec insertion efficiency by SECIS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2016]","start":25800176,"end":25818224,"strand":1,"description":"selenoprotein N [Source:HGNC Symbol;Acc:HGNC:15999]"}, {"versioned_ensembl_gene_id":"ENSG00000279672.1","gene_symbol":"AP006621.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":779617,"end":780755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230249.1","gene_symbol":"AC112653.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3112900,"end":3113596,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240354.1","gene_symbol":"AC131211.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161816909,"end":161821908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231704.5","gene_symbol":"AC004895.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6081103,"end":6093085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211640.4","gene_symbol":"IGLV6-57","gene_name":"immunoglobulin lambda variable 6-57 [Source:HGNC Symbol;Acc:HGNC:5927]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28778","summary":null,"start":22195799,"end":22196276,"strand":1,"description":"immunoglobulin lambda variable 6-57 [Source:HGNC Symbol;Acc:HGNC:5927]"}, {"versioned_ensembl_gene_id":"ENSG00000182447.4","gene_symbol":"OTOL1","gene_name":"otolin 1 [Source:HGNC Symbol;Acc:HGNC:34071]","synonyms":"C1QTNF16,C1QTNF15","biotype":"protein_coding","ncbi_id":"131149","summary":"This gene encodes a secreted glycoprotein with a C-terminal complement Cq1-like globular domain that belongs to the C1q/tumor necrosis factor-related protein (CTRP) family. The encoded protein is expressed in the inner ear and forms a multimeric complex called the otoconia, together with cerebellin-1 and otoconin-90, as part of the otoconial membrane. It contains extensive posttranslational modifications including hydroxylated prolines and glycosylated lysines. Naturally occurring mutations in this gene are associated with abnormal otoconia formation and balance deficits resulting from vestibular dysfunction. [provided by RefSeq, Jul 2017]","start":161496808,"end":161503942,"strand":1,"description":"otolin 1 [Source:HGNC Symbol;Acc:HGNC:34071]"}, {"versioned_ensembl_gene_id":"ENSG00000051128.18","gene_symbol":"HOMER3","gene_name":"homer scaffolding protein 3 [Source:HGNC Symbol;Acc:HGNC:17514]","synonyms":"HOMER-3","biotype":"protein_coding","ncbi_id":"9454","summary":"This gene encodes a member of the HOMER family of postsynaptic density scaffolding proteins that share a similar domain structure consisting of an N-terminal Enabled/vasodilator-stimulated phosphoprotein homology 1 domain which mediates protein-protein interactions, and a carboxy-terminal coiled-coil domain and two leucine zipper motifs that are involved in self-oligomerization. The encoded protein binds numerous other proteins including group I metabotropic glutamate receptors, inositol 1,4,5-trisphosphate receptors and amyloid precursor proteins and has been implicated in diverse biological functions such as neuronal signaling, T-cell activation and trafficking of amyloid beta peptides. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]","start":18929201,"end":18941261,"strand":-1,"description":"homer scaffolding protein 3 [Source:HGNC Symbol;Acc:HGNC:17514]"}, {"versioned_ensembl_gene_id":"ENSG00000233857.5","gene_symbol":"LINC01015","gene_name":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507362","summary":null,"start":29529209,"end":29533357,"strand":1,"description":"long intergenic non-protein coding RNA 1015 [Source:HGNC Symbol;Acc:HGNC:48988]"}, {"versioned_ensembl_gene_id":"ENSG00000274692.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769275,"end":54783790,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000156162.16","gene_symbol":"DPY19L4","gene_name":"dpy-19 like 4 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:27829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"286148","summary":null,"start":94719703,"end":94793836,"strand":1,"description":"dpy-19 like 4 (C. elegans) [Source:HGNC Symbol;Acc:HGNC:27829]"}, {"versioned_ensembl_gene_id":"ENSG00000260402.1","gene_symbol":"AC133485.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32262827,"end":32265514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244926.6","gene_symbol":"ALKBH3-AS1","gene_name":"ALKBH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48670]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507300","summary":null,"start":43909292,"end":43920944,"strand":-1,"description":"ALKBH3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48670]"}, {"versioned_ensembl_gene_id":"ENSG00000227886.1","gene_symbol":"CR759768.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":29497291,"end":29510338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268193.5","gene_symbol":"AC002985.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18907013,"end":18934397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178171.10","gene_symbol":"AMER3","gene_name":"APC membrane recruitment protein 3 [Source:HGNC Symbol;Acc:HGNC:26771]","synonyms":"FLJ38377,FAM123C","biotype":"protein_coding","ncbi_id":"205147","summary":null,"start":130755435,"end":130768134,"strand":1,"description":"APC membrane recruitment protein 3 [Source:HGNC Symbol;Acc:HGNC:26771]"}, {"versioned_ensembl_gene_id":"ENSG00000237918.9","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"NG23,C6orf26","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31753556,"end":31755608,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000183542.5","gene_symbol":"KLRC4","gene_name":"killer cell lectin like receptor C4 [Source:HGNC Symbol;Acc:HGNC:6377]","synonyms":"NKG2-F","biotype":"protein_coding","ncbi_id":"8302","summary":"Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. This gene is a member of the NKG2 group of genes that are expressed primarily in natural killer (NK) cells. These family members encode transmembrane proteins that are characterized by a type II membrane orientation (have an extracellular C-terminus) and the presence of a C-type lectin domain. This family member is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed in NK cells. Read-through transcription exists between this gene and the downstream KLRK1 (killer cell lectin-like receptor subfamily K, member 1) family member. [provided by RefSeq, Dec 2010]","start":10407382,"end":10409757,"strand":-1,"description":"killer cell lectin like receptor C4 [Source:HGNC Symbol;Acc:HGNC:6377]"}, {"versioned_ensembl_gene_id":"ENSG00000105576.15","gene_symbol":"TNPO2","gene_name":"transportin 2 [Source:HGNC Symbol;Acc:HGNC:19998]","synonyms":"TRN2,KPNB2B,IPO3,FLJ12155","biotype":"protein_coding","ncbi_id":"30000","summary":null,"start":12699194,"end":12724011,"strand":-1,"description":"transportin 2 [Source:HGNC Symbol;Acc:HGNC:19998]"}, {"versioned_ensembl_gene_id":"ENSG00000280577.1","gene_symbol":"OR8L1P","gene_name":"olfactory receptor family 8 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15316]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81164","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":56389241,"end":56390195,"strand":1,"description":"olfactory receptor family 8 subfamily L member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15316]"}, {"versioned_ensembl_gene_id":"ENSG00000253823.1","gene_symbol":"IGLV1-62","gene_name":"immunoglobulin lambda variable 1-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5883]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28819","summary":null,"start":22086561,"end":22087110,"strand":1,"description":"immunoglobulin lambda variable 1-62 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5883]"}, {"versioned_ensembl_gene_id":"ENSG00000254094.1","gene_symbol":"AC078852.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1356581,"end":1358075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203801.8","gene_symbol":"LINC00222","gene_name":"long intergenic non-protein coding RNA 222 [Source:HGNC Symbol;Acc:HGNC:21560]","synonyms":"NCRNA00222,dJ354J5.2,C6orf181","biotype":"lincRNA","ncbi_id":"387111","summary":null,"start":108751654,"end":108769942,"strand":1,"description":"long intergenic non-protein coding RNA 222 [Source:HGNC Symbol;Acc:HGNC:21560]"}, {"versioned_ensembl_gene_id":"ENSG00000271272.1","gene_symbol":"AC068802.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42929848,"end":42930579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253126.1","gene_symbol":"IGLVI-56","gene_name":"immunoglobulin lambda variable (I)-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5937]","synonyms":"IGLV(I)-56","biotype":"IG_V_pseudogene","ncbi_id":"28766","summary":null,"start":22198560,"end":22199011,"strand":1,"description":"immunoglobulin lambda variable (I)-56 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5937]"}, {"versioned_ensembl_gene_id":"ENSG00000253637.1","gene_symbol":"IGLVV-58","gene_name":"immunoglobulin lambda variable (V)-58 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5945]","synonyms":"IGLV(V)-58","biotype":"IG_V_pseudogene","ncbi_id":"28758","summary":null,"start":22182582,"end":22182885,"strand":1,"description":"immunoglobulin lambda variable (V)-58 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5945]"}, {"versioned_ensembl_gene_id":"ENSG00000184108.7","gene_symbol":"TRIML1","gene_name":"tripartite motif family like 1 [Source:HGNC Symbol;Acc:HGNC:26698]","synonyms":"RNF209,FLJ36180","biotype":"protein_coding","ncbi_id":"339976","summary":"The protein encoded by this gene is a tripartite motif family protein with similarities to E3 ubiquitin-protein ligases. While the function of the encoded protein has not been determined, the orthologous protein in mouse has been shown to bind ubiquitin-specific protease 5 and is involved in the blastocyst development stage. [provided by RefSeq, Sep 2016]","start":188139419,"end":188147743,"strand":1,"description":"tripartite motif family like 1 [Source:HGNC Symbol;Acc:HGNC:26698]"}, {"versioned_ensembl_gene_id":"ENSG00000101138.11","gene_symbol":"CSTF1","gene_name":"cleavage stimulation factor subunit 1 [Source:HGNC Symbol;Acc:HGNC:2483]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1477","summary":"This gene encodes one of three subunits which combine to form cleavage stimulation factor (CSTF). CSTF is involved in the polyadenylation and 3'end cleavage of pre-mRNAs. Similar to mammalian G protein beta subunits, this protein contains transducin-like repeats. Several transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]","start":56392371,"end":56406369,"strand":1,"description":"cleavage stimulation factor subunit 1 [Source:HGNC Symbol;Acc:HGNC:2483]"}, {"versioned_ensembl_gene_id":"ENSG00000254161.1","gene_symbol":"IGLVIV-65","gene_name":"immunoglobulin lambda variable (IV)-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5944]","synonyms":"IGLV(IV)-65","biotype":"IG_V_pseudogene","ncbi_id":"28759","summary":null,"start":22070225,"end":22070707,"strand":1,"description":"immunoglobulin lambda variable (IV)-65 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5944]"}, {"versioned_ensembl_gene_id":"ENSG00000253874.1","gene_symbol":"IGLVIV-66-1","gene_name":"immunoglobulin lambda variable (IV)-66-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15692]","synonyms":"IGLV(IV)-66-1","biotype":"IG_V_pseudogene","ncbi_id":"84097","summary":null,"start":22058433,"end":22058892,"strand":1,"description":"immunoglobulin lambda variable (IV)-66-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:15692]"}, {"versioned_ensembl_gene_id":"ENSG00000211639.2","gene_symbol":"IGLV4-60","gene_name":"immunoglobulin lambda variable 4-60 [Source:HGNC Symbol;Acc:HGNC:5920]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28785","summary":null,"start":22162199,"end":22162681,"strand":1,"description":"immunoglobulin lambda variable 4-60 [Source:HGNC Symbol;Acc:HGNC:5920]"}, {"versioned_ensembl_gene_id":"ENSG00000172146.2","gene_symbol":"OR1A1","gene_name":"olfactory receptor family 1 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8179]","synonyms":"OR17-7","biotype":"protein_coding","ncbi_id":"8383","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3207539,"end":3218896,"strand":1,"description":"olfactory receptor family 1 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8179]"}, {"versioned_ensembl_gene_id":"ENSG00000143157.11","gene_symbol":"POGK","gene_name":"pogo transposable element derived with KRAB domain [Source:HGNC Symbol;Acc:HGNC:18800]","synonyms":"LST003,KRBOX2,KIAA15131,BASS2","biotype":"protein_coding","ncbi_id":"57645","summary":"The exact function of the protein encoded by this gene is not known. However, this gene product contains a KRAB domain (which is involved in protein-protein interactions) at the N-terminus, and a transposase domain at the C-terminus, suggesting that it may belong to the family of DNA-mediated transposons in human. [provided by RefSeq, Jul 2008]","start":166839447,"end":166856344,"strand":1,"description":"pogo transposable element derived with KRAB domain [Source:HGNC Symbol;Acc:HGNC:18800]"}, {"versioned_ensembl_gene_id":"ENSG00000163870.14","gene_symbol":"TPRA1","gene_name":"transmembrane protein adipocyte associated 1 [Source:HGNC Symbol;Acc:HGNC:30413]","synonyms":"TPRA40,TMEM227,GPR175,FLJ32197","biotype":"protein_coding","ncbi_id":"131601","summary":null,"start":127573069,"end":127598251,"strand":-1,"description":"transmembrane protein adipocyte associated 1 [Source:HGNC Symbol;Acc:HGNC:30413]"}, {"versioned_ensembl_gene_id":"ENSG00000187650.3","gene_symbol":"VMAC","gene_name":"vimentin type intermediate filament associated coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:33803]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400673","summary":null,"start":5904858,"end":5910853,"strand":1,"description":"vimentin type intermediate filament associated coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:33803]"}, {"versioned_ensembl_gene_id":"ENSG00000165271.16","gene_symbol":"NOL6","gene_name":"nucleolar protein 6 [Source:HGNC Symbol;Acc:HGNC:19910]","synonyms":"UTP22,Nrap,MGC20838,MGC14921,MGC14896,FLJ21959,bA311H10.1","biotype":"protein_coding","ncbi_id":"65083","summary":"The nucleolus is a dense subnuclear membraneless organelle that assembles around clusters of rRNA genes and functions in ribosome biogenesis. This gene encodes a nucleolar RNA-associated protein that is highly conserved between species. RNase treatment of permeabilized cells indicates that the nucleolar localization is RNA dependent. Further studies suggest that the protein is associated with ribosome biogenesis through an interaction with pre-rRNA primary transcripts. Alternative splicing has been observed at this locus and two splice variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]","start":33461441,"end":33473930,"strand":-1,"description":"nucleolar protein 6 [Source:HGNC Symbol;Acc:HGNC:19910]"}, {"versioned_ensembl_gene_id":"ENSG00000135709.12","gene_symbol":"KIAA0513","gene_name":"KIAA0513 [Source:HGNC Symbol;Acc:HGNC:29058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9764","summary":null,"start":85027751,"end":85094230,"strand":1,"description":"KIAA0513 [Source:HGNC Symbol;Acc:HGNC:29058]"}, {"versioned_ensembl_gene_id":"ENSG00000261049.2","gene_symbol":"AC007347.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54033997,"end":54054583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259365.1","gene_symbol":"AC019254.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":101116603,"end":101117546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275191.1","gene_symbol":"AC007497.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":53628256,"end":53628816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281650.1","gene_symbol":"AC243922.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":70448301,"end":70556133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269886.1","gene_symbol":"AC022382.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9812762,"end":9813097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197099.8","gene_symbol":"AC068631.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":186579476,"end":186772986,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206412.6","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30605288,"end":30617469,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000225972.1","gene_symbol":"MTND1P23","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42092]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100887749","summary":null,"start":629062,"end":629433,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:42092]"}, {"versioned_ensembl_gene_id":"ENSG00000186844.5","gene_symbol":"LCE1A","gene_name":"late cornified envelope 1A [Source:HGNC Symbol;Acc:HGNC:29459]","synonyms":"LEP1","biotype":"protein_coding","ncbi_id":"353131","summary":"LCE1A belongs to the late cornified envelope (LCE) gene cluster within the epidermal differentiation complex (EDC) on chromosome 1. The LCE cluster contains multiple conserved genes that encode stratum corneum proteins, and these genes are expressed relatively late during fetal assembly of the skin cornified envelope (Jackson et al., 2005 [PubMed 15854049]). For further information on the LCE gene cluster, see GENE FAMILY below.[supplied by OMIM, Feb 2009]","start":152827473,"end":152827894,"strand":1,"description":"late cornified envelope 1A [Source:HGNC Symbol;Acc:HGNC:29459]"}, {"versioned_ensembl_gene_id":"ENSG00000242636.1","gene_symbol":"RPL21P129","gene_name":"ribosomal protein L21 pseudogene 129 [Source:HGNC Symbol;Acc:HGNC:36747]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271451","summary":null,"start":7750684,"end":7751161,"strand":1,"description":"ribosomal protein L21 pseudogene 129 [Source:HGNC Symbol;Acc:HGNC:36747]"}, {"versioned_ensembl_gene_id":"ENSG00000230722.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29748177,"end":29748597,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000230021.9","gene_symbol":"AL669831.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":586071,"end":827796,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249850.1","gene_symbol":"KRT18P31","gene_name":"keratin 18 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:33400]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646723","summary":null,"start":36885206,"end":36886497,"strand":1,"description":"keratin 18 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:33400]"}, {"versioned_ensembl_gene_id":"ENSG00000229344.1","gene_symbol":"MTCO2P12","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52028]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075310","summary":null,"start":632757,"end":633438,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52028]"}, {"versioned_ensembl_gene_id":"ENSG00000163959.9","gene_symbol":"SLC51A","gene_name":"solute carrier family 51 alpha subunit [Source:HGNC Symbol;Acc:HGNC:29955]","synonyms":"OSTalpha","biotype":"protein_coding","ncbi_id":"200931","summary":null,"start":196211487,"end":196243178,"strand":1,"description":"solute carrier family 51 alpha subunit [Source:HGNC Symbol;Acc:HGNC:29955]"}, {"versioned_ensembl_gene_id":"ENSG00000065150.18","gene_symbol":"IPO5","gene_name":"importin 5 [Source:HGNC Symbol;Acc:HGNC:6402]","synonyms":"RANBP5,Pse1,MGC2068,KPNB3,IMB3","biotype":"protein_coding","ncbi_id":"3843","summary":"Nucleocytoplasmic transport, a signal- and energy-dependent process, takes place through nuclear pore complexes embedded in the nuclear envelope. The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor, a heterodimer of importin alpha and beta subunits also known as karyopherins. Importin alpha binds the NLS-containing cargo in the cytoplasm and importin beta docks the complex at the cytoplasmic side of the nuclear pore complex. In the presence of nucleoside triphosphates and the small GTP binding protein Ran, the complex moves into the nuclear pore complex and the importin subunits dissociate. Importin alpha enters the nucleoplasm with its passenger protein and importin beta remains at the pore. Interactions between importin beta and the FG repeats of nucleoporins are essential in translocation through the pore complex. The protein encoded by this gene is a member of the importin beta family. [provided by RefSeq, Jul 2008]","start":97953658,"end":98024297,"strand":1,"description":"importin 5 [Source:HGNC Symbol;Acc:HGNC:6402]"}, {"versioned_ensembl_gene_id":"ENSG00000232217.1","gene_symbol":"FTLP8","gene_name":"ferritin light chain pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37956]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462790","summary":null,"start":97986950,"end":97987216,"strand":-1,"description":"ferritin light chain pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37956]"}, {"versioned_ensembl_gene_id":"ENSG00000226312.7","gene_symbol":"CFLAR-AS1","gene_name":"CFLAR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:14437]","synonyms":"ALS2CR10","biotype":"antisense_RNA","ncbi_id":"65072","summary":null,"start":201140278,"end":201157823,"strand":-1,"description":"CFLAR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:14437]"}, {"versioned_ensembl_gene_id":"ENSG00000235579.1","gene_symbol":"AC007283.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":201162484,"end":201162680,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232133.1","gene_symbol":"IMPDH1P10","gene_name":"inosine monophosphate dehydrogenase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:33965]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874399","summary":null,"start":201137516,"end":201140027,"strand":-1,"description":"inosine monophosphate dehydrogenase 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:33965]"}, {"versioned_ensembl_gene_id":"ENSG00000122873.11","gene_symbol":"CISD1","gene_name":"CDGSH iron sulfur domain 1 [Source:HGNC Symbol;Acc:HGNC:30880]","synonyms":"ZCD1,mitoNEET,MDS029,C10orf70","biotype":"protein_coding","ncbi_id":"55847","summary":"This gene encodes a protein with a CDGSH iron-sulfur domain and has been shown to bind a redox-active [2Fe-2S] cluster. The encoded protein has been localized to the outer membrane of mitochondria and is thought to play a role in regulation of oxidation. Genes encoding similar proteins are located on chromosomes 4 and 17, and a pseudogene of this gene is located on chromosome 2. [provided by RefSeq, Feb 2012]","start":58269058,"end":58289586,"strand":1,"description":"CDGSH iron sulfur domain 1 [Source:HGNC Symbol;Acc:HGNC:30880]"}, {"versioned_ensembl_gene_id":"ENSG00000172006.11","gene_symbol":"ZNF554","gene_name":"zinc finger protein 554 [Source:HGNC Symbol;Acc:HGNC:26629]","synonyms":"FLJ34817","biotype":"protein_coding","ncbi_id":"115196","summary":null,"start":2819874,"end":2835773,"strand":1,"description":"zinc finger protein 554 [Source:HGNC Symbol;Acc:HGNC:26629]"}, {"versioned_ensembl_gene_id":"ENSG00000228327.3","gene_symbol":"AL669831.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":725885,"end":778626,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237973.1","gene_symbol":"MTCO1P12","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52014]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075141","summary":null,"start":631074,"end":632616,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:52014]"}, {"versioned_ensembl_gene_id":"ENSG00000225630.1","gene_symbol":"MTND2P28","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42129]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100652939","summary":null,"start":629640,"end":630683,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42129]"}, {"versioned_ensembl_gene_id":"ENSG00000240409.1","gene_symbol":"MTATP8P1","gene_name":"mitochondrially encoded ATP synthase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44571]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480795","summary":null,"start":633535,"end":633741,"strand":1,"description":"mitochondrially encoded ATP synthase 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44571]"}, {"versioned_ensembl_gene_id":"ENSG00000233570.1","gene_symbol":"LINC00690","gene_name":"long intergenic non-protein coding RNA 690 [Source:HGNC Symbol;Acc:HGNC:44503]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996597","summary":null,"start":16536320,"end":16541373,"strand":1,"description":"long intergenic non-protein coding RNA 690 [Source:HGNC Symbol;Acc:HGNC:44503]"}, {"versioned_ensembl_gene_id":"ENSG00000269391.1","gene_symbol":"AC010139.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16530771,"end":16531802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145107.15","gene_symbol":"TM4SF19","gene_name":"transmembrane 4 L six family member 19 [Source:HGNC Symbol;Acc:HGNC:25167]","synonyms":null,"biotype":"protein_coding","ncbi_id":"116211","summary":"The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017]","start":196319342,"end":196338503,"strand":-1,"description":"transmembrane 4 L six family member 19 [Source:HGNC Symbol;Acc:HGNC:25167]"}, {"versioned_ensembl_gene_id":"ENSG00000268873.1","gene_symbol":"AC022601.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34737795,"end":34767663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256196.1","gene_symbol":"AP003721.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60918469,"end":60925397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184423.5","gene_symbol":"RPL23AP38","gene_name":"ribosomal protein L23a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36351]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391504","summary":null,"start":1595777,"end":1596245,"strand":-1,"description":"ribosomal protein L23a pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:36351]"}, {"versioned_ensembl_gene_id":"ENSG00000112290.12","gene_symbol":"WASF1","gene_name":"WAS protein family member 1 [Source:HGNC Symbol;Acc:HGNC:12732]","synonyms":"WAVE1,WAVE,SCAR1,KIAA0269","biotype":"protein_coding","ncbi_id":"8936","summary":"The protein encoded by this gene, a member of the Wiskott-Aldrich syndrome protein (WASP)-family, plays a critical role downstream of Rac, a Rho-family small GTPase, in regulating the actin cytoskeleton required for membrane ruffling. It has been shown to associate with an actin nucleation core Arp2/3 complex while enhancing actin polymerization in vitro. Wiskott-Aldrich syndrome is a disease of the immune system, likely due to defects in regulation of actin cytoskeleton. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":110099819,"end":110180004,"strand":-1,"description":"WAS protein family member 1 [Source:HGNC Symbol;Acc:HGNC:12732]"}, {"versioned_ensembl_gene_id":"ENSG00000183396.3","gene_symbol":"TMEM89","gene_name":"transmembrane protein 89 [Source:HGNC Symbol;Acc:HGNC:32372]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440955","summary":null,"start":48620759,"end":48621855,"strand":-1,"description":"transmembrane protein 89 [Source:HGNC Symbol;Acc:HGNC:32372]"}, {"versioned_ensembl_gene_id":"ENSG00000122126.15","gene_symbol":"OCRL","gene_name":"OCRL, inositol polyphosphate-5-phosphatase [Source:HGNC Symbol;Acc:HGNC:8108]","synonyms":"OCRL1","biotype":"protein_coding","ncbi_id":"4952","summary":"This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":129539849,"end":129592561,"strand":1,"description":"OCRL, inositol polyphosphate-5-phosphatase [Source:HGNC Symbol;Acc:HGNC:8108]"}, {"versioned_ensembl_gene_id":"ENSG00000213331.4","gene_symbol":"AC108073.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":187970273,"end":187971284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240919.1","gene_symbol":"AC022034.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53532908,"end":53533704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260847.1","gene_symbol":"AC133485.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32188333,"end":32193530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274167.4","gene_symbol":"AL031601.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":42242721,"end":42276842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271650.1","gene_symbol":"AL031601.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42209990,"end":42210383,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227896.2","gene_symbol":"AL731569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":86521945,"end":86525101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101457.12","gene_symbol":"DNTTIP1","gene_name":"deoxynucleotidyltransferase terminal interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16160]","synonyms":"Tdif1,dJ447F3.4,C20orf167","biotype":"protein_coding","ncbi_id":"116092","summary":"DNTTIP1 binds DNA and enhances the activity of terminal deoxynucleotidyltransferase (TDT, or DNTT; MIM 187410), a DNA polymerase that catalyzes the polymerization of DNA in the absence of a DNA template (Yamashita et al., 2001 [PubMed 11473582]).[supplied by OMIM, Mar 2008]","start":45791937,"end":45811427,"strand":1,"description":"deoxynucleotidyltransferase terminal interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:16160]"}, {"versioned_ensembl_gene_id":"ENSG00000275436.5","gene_symbol":"GU182351.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771163,"end":54780643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237592.2","gene_symbol":"IGKV1OR10-1","gene_name":"immunoglobulin kappa variable 1/OR10-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44978]","synonyms":"IGKV1/OR10-1","biotype":"IG_V_pseudogene","ncbi_id":"642424","summary":null,"start":42185339,"end":42185791,"strand":1,"description":"immunoglobulin kappa variable 1/OR10-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:44978]"}, {"versioned_ensembl_gene_id":"ENSG00000277657.1","gene_symbol":"KIR2DS3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]","synonyms":"nkat7","biotype":"protein_coding","ncbi_id":"3808","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54782575,"end":54796808,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6335]"}, {"versioned_ensembl_gene_id":"ENSG00000275422.1","gene_symbol":"GU182351.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54830833,"end":54834726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275528.2","gene_symbol":"CCL15","gene_name":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]","synonyms":"MIP-5,MIP-1d,Lkn-1,HMRP-2B,HCC-2,SCYL3,SCYA15,NCC-3","biotype":"protein_coding","ncbi_id":"6359","summary":"This gene is located in a cluster of similar genes in the same region of chromosome 17. These genes encode CC cytokines, which are secreted proteins characterized by two adjacent cysteines. The product of this gene is chemotactic for T cells and monocytes, and acts through C-C chemokine receptor type 1 (CCR1). The proprotein is further processed into numerous smaller functional peptides. Naturally-occurring readthrough transcripts occur from this gene into the downstream gene, CCL14 (chemokine (C-C motif) ligand 14). [provided by RefSeq, Jan 2013]","start":35996472,"end":36002080,"strand":-1,"description":"C-C motif chemokine ligand 15 [Source:HGNC Symbol;Acc:HGNC:10613]"}, {"versioned_ensembl_gene_id":"ENSG00000178836.6","gene_symbol":"AC114812.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":233754305,"end":233755345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273883.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000244122.2","gene_symbol":"UGT1A7","gene_name":"UDP glucuronosyltransferase family 1 member A7 [Source:HGNC Symbol;Acc:HGNC:12539]","synonyms":"UGT1G","biotype":"protein_coding","ncbi_id":"54577","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has moderate glucuronidase activity with phenols. [provided by RefSeq, Jul 2008]","start":233681938,"end":233773299,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A7 [Source:HGNC Symbol;Acc:HGNC:12539]"}, {"versioned_ensembl_gene_id":"ENSG00000248705.1","gene_symbol":"AC114812.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":233750617,"end":233753656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138135.6","gene_symbol":"CH25H","gene_name":"cholesterol 25-hydroxylase [Source:HGNC Symbol;Acc:HGNC:1907]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9023","summary":"This is an intronless gene that is involved in cholesterol and lipid metabolism. The encoded protein is a membrane protein and contains clusters of histidine residues essential for catalytic activity. Unlike most other sterol hydroxylases, this enzyme is a member of a small family of enzymes that utilize diiron cofactors to catalyze the hydroxylation of hydrophobic substrates. [provided by RefSeq, Jul 2008]","start":89205629,"end":89207314,"strand":-1,"description":"cholesterol 25-hydroxylase [Source:HGNC Symbol;Acc:HGNC:1907]"}, {"versioned_ensembl_gene_id":"ENSG00000233445.1","gene_symbol":"RPL17P11","gene_name":"ribosomal protein L17 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36509]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270937","summary":null,"start":233721522,"end":233722065,"strand":-1,"description":"ribosomal protein L17 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36509]"}, {"versioned_ensembl_gene_id":"ENSG00000228884.2","gene_symbol":"RPL23AP26","gene_name":"ribosomal protein L23a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35592]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391490","summary":null,"start":231585864,"end":231586327,"strand":1,"description":"ribosomal protein L23a pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:35592]"}, {"versioned_ensembl_gene_id":"ENSG00000279592.1","gene_symbol":"AC010653.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":71859680,"end":71860676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112218.8","gene_symbol":"GPR63","gene_name":"G protein-coupled receptor 63 [Source:HGNC Symbol;Acc:HGNC:13302]","synonyms":"PSP24B,PSP24(beta)","biotype":"protein_coding","ncbi_id":"81491","summary":"This gene encodes a G protein-coupled receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011]","start":96794126,"end":96837463,"strand":-1,"description":"G protein-coupled receptor 63 [Source:HGNC Symbol;Acc:HGNC:13302]"}, {"versioned_ensembl_gene_id":"ENSG00000255885.1","gene_symbol":"AC124891.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7870852,"end":7871370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115159.15","gene_symbol":"GPD2","gene_name":"glycerol-3-phosphate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:4456]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2820","summary":"The protein encoded by this gene localizes to the inner mitochondrial membrane and catalyzes the conversion of glycerol-3-phosphate to dihydroxyacetone phosphate, using FAD as a cofactor. Along with GDP1, the encoded protein constitutes the glycerol phosphate shuttle, which reoxidizes NADH formed during glycolysis. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Jan 2010]","start":156435290,"end":156613735,"strand":1,"description":"glycerol-3-phosphate dehydrogenase 2 [Source:HGNC Symbol;Acc:HGNC:4456]"}, {"versioned_ensembl_gene_id":"ENSG00000261765.1","gene_symbol":"AC009127.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":71881553,"end":71882273,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279954.1","gene_symbol":"BX324167.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45875932,"end":45879247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235091.1","gene_symbol":"BX324167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45875999,"end":45887748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205336.11","gene_symbol":"ADGRG1","gene_name":"adhesion G protein-coupled receptor G1 [Source:HGNC Symbol;Acc:HGNC:4512]","synonyms":"TM7XN1,TM7LN4,GPR56","biotype":"protein_coding","ncbi_id":"9289","summary":"This gene encodes a member of the G protein-coupled receptor family and regulates brain cortical patterning. The encoded protein binds specifically to transglutaminase 2, a component of tissue and tumor stroma implicated as an inhibitor of tumor progression. Mutations in this gene are associated with a brain malformation known as bilateral frontoparietal polymicrogyria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":57610652,"end":57665580,"strand":1,"description":"adhesion G protein-coupled receptor G1 [Source:HGNC Symbol;Acc:HGNC:4512]"}, {"versioned_ensembl_gene_id":"ENSG00000242176.1","gene_symbol":"AC009127.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71991151,"end":71991305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106636.7","gene_symbol":"YKT6","gene_name":"YKT6 v-SNARE homolog [Source:HGNC Symbol;Acc:HGNC:16959]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10652","summary":"This gene product is one of the SNARE recognition molecules implicated in vesicular transport between secretory compartments. It is a membrane associated, isoprenylated protein that functions at the endoplasmic reticulum-Golgi transport step. This protein is highly conserved from yeast to human and can functionally complement the loss of the yeast homolog in the yeast secretory pathway. [provided by RefSeq, Jul 2008]","start":44200968,"end":44214294,"strand":1,"description":"YKT6 v-SNARE homolog [Source:HGNC Symbol;Acc:HGNC:16959]"}, {"versioned_ensembl_gene_id":"ENSG00000261781.1","gene_symbol":"LINC01654","gene_name":"long intergenic non-protein coding RNA 1654 [Source:HGNC Symbol;Acc:HGNC:52442]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927876","summary":null,"start":18065657,"end":18074412,"strand":1,"description":"long intergenic non-protein coding RNA 1654 [Source:HGNC Symbol;Acc:HGNC:52442]"}, {"versioned_ensembl_gene_id":"ENSG00000274763.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724452,"end":54736131,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000279783.1","gene_symbol":"AC018692.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9810501,"end":9810848,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140416.19","gene_symbol":"TPM1","gene_name":"tropomyosin 1 [Source:HGNC Symbol;Acc:HGNC:12010]","synonyms":"C15orf13,CMH3","biotype":"protein_coding","ncbi_id":"7168","summary":"This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]","start":63042632,"end":63071915,"strand":1,"description":"tropomyosin 1 [Source:HGNC Symbol;Acc:HGNC:12010]"}, {"versioned_ensembl_gene_id":"ENSG00000144589.21","gene_symbol":"STK11IP","gene_name":"serine/threonine kinase 11 interacting protein [Source:HGNC Symbol;Acc:HGNC:19184]","synonyms":"STK11IP1,LKB1IP,LIP1,KIAA1898","biotype":"protein_coding","ncbi_id":"114790","summary":null,"start":219597860,"end":219616451,"strand":1,"description":"serine/threonine kinase 11 interacting protein [Source:HGNC Symbol;Acc:HGNC:19184]"}, {"versioned_ensembl_gene_id":"ENSG00000137942.16","gene_symbol":"FNBP1L","gene_name":"formin binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:20851]","synonyms":"TOCA1,FLJ20275,C1orf39","biotype":"protein_coding","ncbi_id":"54874","summary":"The protein encoded by this gene binds to both CDC42 and N-WASP. This protein promotes CDC42-induced actin polymerization by activating the N-WASP-WIP complex and, therefore, is involved in a pathway that links cell surface signals to the actin cytoskeleton. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":93448131,"end":93554661,"strand":1,"description":"formin binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:20851]"}, {"versioned_ensembl_gene_id":"ENSG00000279211.1","gene_symbol":"AC124864.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9580024,"end":9580415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188529.14","gene_symbol":"SRSF10","gene_name":"serine and arginine rich splicing factor 10 [Source:HGNC Symbol;Acc:HGNC:16713]","synonyms":"TASR2,TASR1,SRrp40,SRp38,SFRS13A,SFRS13,PPP1R149,FUSIP2,FUSIP1","biotype":"protein_coding","ncbi_id":"10772","summary":"This gene product is a member of the serine-arginine (SR) family of proteins, which are involved in constitutive and regulated RNA splicing. Members of this family are characterized by N-terminal RNP1 and RNP2 motifs, which are required for binding to RNA, and multiple C-terminal SR/RS repeats, which are important in mediating association with other cellular proteins. This protein interacts with the oncoprotein TLS, and abrogates the influence of TLS on adenovirus E1A pre-mRNA splicing. This gene has pseudogenes on chromosomes 4, 9, 14, 18, and 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":23964804,"end":23980927,"strand":-1,"description":"serine and arginine rich splicing factor 10 [Source:HGNC Symbol;Acc:HGNC:16713]"}, {"versioned_ensembl_gene_id":"ENSG00000282490.1","gene_symbol":"AC245594.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39309931,"end":39310465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229635.1","gene_symbol":"AL137159.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93384487,"end":93384998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124602.9","gene_symbol":"UNC5CL","gene_name":"unc-5 family C-terminal like [Source:HGNC Symbol;Acc:HGNC:21203]","synonyms":"ZUD,MGC34763","biotype":"protein_coding","ncbi_id":"222643","summary":null,"start":41026911,"end":41039217,"strand":-1,"description":"unc-5 family C-terminal like [Source:HGNC Symbol;Acc:HGNC:21203]"}, {"versioned_ensembl_gene_id":"ENSG00000249522.1","gene_symbol":"AC147876.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3910283,"end":3910604,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138760.9","gene_symbol":"SCARB2","gene_name":"scavenger receptor class B member 2 [Source:HGNC Symbol;Acc:HGNC:1665]","synonyms":"CD36L2,SR-BII,LIMPII,LIMP-2,HLGP85","biotype":"protein_coding","ncbi_id":"950","summary":"The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]","start":76158733,"end":76234536,"strand":-1,"description":"scavenger receptor class B member 2 [Source:HGNC Symbol;Acc:HGNC:1665]"}, {"versioned_ensembl_gene_id":"ENSG00000266801.1","gene_symbol":"AC009137.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":68933820,"end":68937725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144713.12","gene_symbol":"RPL32","gene_name":"ribosomal protein L32 [Source:HGNC Symbol;Acc:HGNC:10336]","synonyms":"L32","biotype":"protein_coding","ncbi_id":"6161","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L32E family of ribosomal proteins. It is located in the cytoplasm. Although some studies have mapped this gene to 3q13.3-q21, it is believed to map to 3p25-p24. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternatively spliced transcript variants encoding the same protein have been observed for this gene. [provided by RefSeq, Jul 2008]","start":12834485,"end":12841588,"strand":-1,"description":"ribosomal protein L32 [Source:HGNC Symbol;Acc:HGNC:10336]"}, {"versioned_ensembl_gene_id":"ENSG00000272263.1","gene_symbol":"AC034198.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12832219,"end":12832728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103047.7","gene_symbol":"TANGO6","gene_name":"transport and golgi organization 6 homolog [Source:HGNC Symbol;Acc:HGNC:25749]","synonyms":"TMCO7,KIAA1746,FLJ12688","biotype":"protein_coding","ncbi_id":"79613","summary":null,"start":68843604,"end":69085180,"strand":1,"description":"transport and golgi organization 6 homolog [Source:HGNC Symbol;Acc:HGNC:25749]"}, {"versioned_ensembl_gene_id":"ENSG00000251271.3","gene_symbol":"ALG1L7P","gene_name":"asparagine-linked glycosylation 1-like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44376]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"728263","summary":null,"start":3935447,"end":3942519,"strand":1,"description":"asparagine-linked glycosylation 1-like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44376]"}, {"versioned_ensembl_gene_id":"ENSG00000271129.1","gene_symbol":"AC009027.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":69025860,"end":69026643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260999.1","gene_symbol":"AC009137.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68927547,"end":68948261,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244378.1","gene_symbol":"RPS2P45","gene_name":"ribosomal protein S2 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:25709]","synonyms":"FLJ12331","biotype":"transcribed_processed_pseudogene","ncbi_id":"80052","summary":null,"start":69033675,"end":69036042,"strand":1,"description":"ribosomal protein S2 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:25709]"}, {"versioned_ensembl_gene_id":"ENSG00000244474.5","gene_symbol":"UGT1A4","gene_name":"UDP glucuronosyltransferase family 1 member A4 [Source:HGNC Symbol;Acc:HGNC:12536]","synonyms":"UGT1D,HUG-BR2","biotype":"protein_coding","ncbi_id":"54657","summary":"This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. This enzyme has some glucuronidase activity towards bilirubin, although is is more active on amines, steroids, and sapogenins. [provided by RefSeq, Jul 2008]","start":233718778,"end":233773299,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A4 [Source:HGNC Symbol;Acc:HGNC:12536]"}, {"versioned_ensembl_gene_id":"ENSG00000224814.1","gene_symbol":"AC114812.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":233693434,"end":233708699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163249.11","gene_symbol":"CCNYL1","gene_name":"cyclin Y like 1 [Source:HGNC Symbol;Acc:HGNC:26868]","synonyms":"FLJ40432","biotype":"protein_coding","ncbi_id":"151195","summary":null,"start":207711540,"end":207761839,"strand":1,"description":"cyclin Y like 1 [Source:HGNC Symbol;Acc:HGNC:26868]"}, {"versioned_ensembl_gene_id":"ENSG00000185101.12","gene_symbol":"ANO9","gene_name":"anoctamin 9 [Source:HGNC Symbol;Acc:HGNC:20679]","synonyms":"TP53I5,TMEM16J,PIG5","biotype":"protein_coding","ncbi_id":"338440","summary":"The protein encoded by this gene is a member of the TMEM16 (anoctamin) family of proteins, some of which form integral membrane calcium-activated chloride channels. The function of the encoded protein has yet to be elucidated, although it may have channel-forming abilities and also may have phospholipid scramblase activity. This gene has been observed to be upregulated in stage II and III colorectal cancers. [provided by RefSeq, Dec 2016]","start":417933,"end":442011,"strand":-1,"description":"anoctamin 9 [Source:HGNC Symbol;Acc:HGNC:20679]"}, {"versioned_ensembl_gene_id":"ENSG00000258112.1","gene_symbol":"CCNG2P1","gene_name":"cyclin G2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50853]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128681","summary":null,"start":75257635,"end":75258634,"strand":-1,"description":"cyclin G2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50853]"}, {"versioned_ensembl_gene_id":"ENSG00000257823.1","gene_symbol":"AC092552.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":75305452,"end":75306357,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134539.16","gene_symbol":"KLRD1","gene_name":"killer cell lectin like receptor D1 [Source:HGNC Symbol;Acc:HGNC:6378]","synonyms":"CD94","biotype":"protein_coding","ncbi_id":"3824","summary":"Natural killer (NK) cells are a distinct lineage of lymphocytes that mediate cytotoxic activity and secrete cytokines upon immune stimulation. Several genes of the C-type lectin superfamily, including members of the NKG2 family, are expressed by NK cells and may be involved in the regulation of NK cell function. KLRD1 (CD94) is an antigen preferentially expressed on NK cells and is classified as a type II membrane protein because it has an external C terminus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2017]","start":10226058,"end":10329600,"strand":1,"description":"killer cell lectin like receptor D1 [Source:HGNC Symbol;Acc:HGNC:6378]"}, {"versioned_ensembl_gene_id":"ENSG00000223560.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30427014,"end":30428182,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000173706.12","gene_symbol":"HEG1","gene_name":"heart development protein with EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:29227]","synonyms":"KIAA1237,HEG","biotype":"protein_coding","ncbi_id":"57493","summary":null,"start":124965710,"end":125055958,"strand":-1,"description":"heart development protein with EGF like domains 1 [Source:HGNC Symbol;Acc:HGNC:29227]"}, {"versioned_ensembl_gene_id":"ENSG00000259738.1","gene_symbol":"ZNF444P1","gene_name":"zinc finger protein 444 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35157]","synonyms":"ZNF864P","biotype":"processed_pseudogene","ncbi_id":"100419866","summary":null,"start":58865006,"end":58865303,"strand":1,"description":"zinc finger protein 444 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35157]"}, {"versioned_ensembl_gene_id":"ENSG00000242747.1","gene_symbol":"AC090515.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58869659,"end":58870134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236080.2","gene_symbol":"YAP1P2","gene_name":"Yes associated protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38017]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419909","summary":null,"start":115069237,"end":115069846,"strand":1,"description":"Yes associated protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38017]"}, {"versioned_ensembl_gene_id":"ENSG00000090661.11","gene_symbol":"CERS4","gene_name":"ceramide synthase 4 [Source:HGNC Symbol;Acc:HGNC:23747]","synonyms":"LASS4,FLJ12089,Trh1","biotype":"protein_coding","ncbi_id":"79603","summary":null,"start":8206736,"end":8262421,"strand":1,"description":"ceramide synthase 4 [Source:HGNC Symbol;Acc:HGNC:23747]"}, {"versioned_ensembl_gene_id":"ENSG00000104299.14","gene_symbol":"INTS9","gene_name":"integrator complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:25592]","synonyms":"RC-74,FLJ10871,CPSF2L","biotype":"protein_coding","ncbi_id":"55756","summary":"This gene encodes a subunit of the Integrator complex. This protein complex binds the C-terminal domain of RNA polymerase II and likely plays a role in small nuclear RNA processing. The encoded protein has similarities to the subunits of the cleavage and polyadenylation specificity factor complex. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]","start":28767661,"end":28890242,"strand":-1,"description":"integrator complex subunit 9 [Source:HGNC Symbol;Acc:HGNC:25592]"}, {"versioned_ensembl_gene_id":"ENSG00000271717.1","gene_symbol":"AC022146.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8222153,"end":8239648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173401.9","gene_symbol":"GLIPR1L1","gene_name":"GLI pathogenesis related 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28392]","synonyms":"MGC26856","biotype":"protein_coding","ncbi_id":"256710","summary":null,"start":75334639,"end":75370560,"strand":1,"description":"GLI pathogenesis related 1 like 1 [Source:HGNC Symbol;Acc:HGNC:28392]"}, {"versioned_ensembl_gene_id":"ENSG00000254034.1","gene_symbol":"INTS9-AS1","gene_name":"INTS9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53139]","synonyms":"ENST00000520055","biotype":"antisense_RNA","ncbi_id":"109729178","summary":null,"start":28798142,"end":28799469,"strand":1,"description":"INTS9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53139]"}, {"versioned_ensembl_gene_id":"ENSG00000142733.14","gene_symbol":"MAP3K6","gene_name":"mitogen-activated protein kinase kinase kinase 6 [Source:HGNC Symbol;Acc:HGNC:6858]","synonyms":"MEKK6,MAPKKK6,ASK2","biotype":"protein_coding","ncbi_id":"9064","summary":"This gene encodes a serine/threonine protein kinase that forms a component of protein kinase-mediated signal transduction cascades. The encoded kinase participates in the regulation of vascular endothelial growth factor (VEGF) expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":27355184,"end":27366892,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase 6 [Source:HGNC Symbol;Acc:HGNC:6858]"}, {"versioned_ensembl_gene_id":"ENSG00000116750.13","gene_symbol":"UCHL5","gene_name":"ubiquitin C-terminal hydrolase L5 [Source:HGNC Symbol;Acc:HGNC:19678]","synonyms":"UCH37,INO80R,CGI-70","biotype":"protein_coding","ncbi_id":"51377","summary":null,"start":193012250,"end":193060080,"strand":-1,"description":"ubiquitin C-terminal hydrolase L5 [Source:HGNC Symbol;Acc:HGNC:19678]"}, {"versioned_ensembl_gene_id":"ENSG00000237807.3","gene_symbol":"AC022034.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53515171,"end":53523931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107731.12","gene_symbol":"UNC5B","gene_name":"unc-5 netrin receptor B [Source:HGNC Symbol;Acc:HGNC:12568]","synonyms":"UNC5H2,p53RDL1","biotype":"protein_coding","ncbi_id":"219699","summary":"This gene encodes a member of the netrin family of receptors. This particular protein mediates the repulsive effect of netrin-1 and is a vascular netrin receptor. This encoded protein is also in a group of proteins called dependence receptors (DpRs) which are involved in pro- and anti-apoptotic processes. Many DpRs are involved in embryogenesis and in cancer progression. Two alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]","start":71212570,"end":71302864,"strand":1,"description":"unc-5 netrin receptor B [Source:HGNC Symbol;Acc:HGNC:12568]"}, {"versioned_ensembl_gene_id":"ENSG00000224279.2","gene_symbol":"RPS29P31","gene_name":"ribosomal protein S29 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52364]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729124","summary":null,"start":38574931,"end":38575431,"strand":-1,"description":"ribosomal protein S29 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:52364]"}, {"versioned_ensembl_gene_id":"ENSG00000085644.13","gene_symbol":"ZNF213","gene_name":"zinc finger protein 213 [Source:HGNC Symbol;Acc:HGNC:13005]","synonyms":"ZSCAN53,ZKSCAN21,CR53","biotype":"protein_coding","ncbi_id":"7760","summary":"C2H2 zinc finger proteins, such as ZNF213, have bipartite structures in which one domain binds DNA or RNA and the other modulates target gene expression.[supplied by OMIM, Apr 2004]","start":3129777,"end":3142805,"strand":1,"description":"zinc finger protein 213 [Source:HGNC Symbol;Acc:HGNC:13005]"}, {"versioned_ensembl_gene_id":"ENSG00000112212.11","gene_symbol":"TSPO2","gene_name":"translocator protein 2 [Source:HGNC Symbol;Acc:HGNC:21256]","synonyms":"dJ34B21.2,BZRPL1","biotype":"protein_coding","ncbi_id":"222642","summary":null,"start":41042554,"end":41044337,"strand":1,"description":"translocator protein 2 [Source:HGNC Symbol;Acc:HGNC:21256]"}, {"versioned_ensembl_gene_id":"ENSG00000164543.5","gene_symbol":"STK17A","gene_name":"serine/threonine kinase 17a [Source:HGNC Symbol;Acc:HGNC:11395]","synonyms":"DRAK1","biotype":"protein_coding","ncbi_id":"9263","summary":"This gene is a member of the DAP kinase-related apoptosis-inducing protein kinase family and encodes an autophosphorylated nuclear protein with a protein kinase domain. The protein has apoptosis-inducing activity. [provided by RefSeq, Jul 2008]","start":43582758,"end":43626786,"strand":1,"description":"serine/threonine kinase 17a [Source:HGNC Symbol;Acc:HGNC:11395]"}, {"versioned_ensembl_gene_id":"ENSG00000248256.1","gene_symbol":"OCIAD1-AS1","gene_name":"OCIAD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40751]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861517","summary":null,"start":48852008,"end":48860203,"strand":-1,"description":"OCIAD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40751]"}, {"versioned_ensembl_gene_id":"ENSG00000124701.5","gene_symbol":"APOBEC2","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:605]","synonyms":"ARCD1,ARP1","biotype":"protein_coding","ncbi_id":"10930","summary":null,"start":41053304,"end":41064511,"strand":1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 2 [Source:HGNC Symbol;Acc:HGNC:605]"}, {"versioned_ensembl_gene_id":"ENSG00000134138.19","gene_symbol":"MEIS2","gene_name":"Meis homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7001]","synonyms":"MRG1,HsT18361","biotype":"protein_coding","ncbi_id":"4212","summary":"This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. TALE homeobox proteins are highly conserved transcription regulators, and several members have been shown to be essential contributors to developmental programs. Multiple transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":36889204,"end":37101299,"strand":-1,"description":"Meis homeobox 2 [Source:HGNC Symbol;Acc:HGNC:7001]"}, {"versioned_ensembl_gene_id":"ENSG00000140988.15","gene_symbol":"RPS2","gene_name":"ribosomal protein S2 [Source:HGNC Symbol;Acc:HGNC:10404]","synonyms":"S2,LLREP3","biotype":"protein_coding","ncbi_id":"6187","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S5P family of ribosomal proteins. It is located in the cytoplasm. This gene shares sequence similarity with mouse LLRep3. It is co-transcribed with the small nucleolar RNA gene U64, which is located in its third intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":1962052,"end":1964860,"strand":-1,"description":"ribosomal protein S2 [Source:HGNC Symbol;Acc:HGNC:10404]"}, {"versioned_ensembl_gene_id":"ENSG00000255513.1","gene_symbol":"AC005363.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":1963745,"end":1964095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279718.1","gene_symbol":"SNX18P12","gene_name":"sorting nexin 18 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419041","summary":null,"start":9364467,"end":9365225,"strand":-1,"description":"sorting nexin 18 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39620]"}, {"versioned_ensembl_gene_id":"ENSG00000259460.1","gene_symbol":"AC078909.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37099339,"end":37100173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166619.12","gene_symbol":"BLCAP","gene_name":"bladder cancer associated protein [Source:HGNC Symbol;Acc:HGNC:1055]","synonyms":"BC10","biotype":"protein_coding","ncbi_id":"10904","summary":"This gene encodes a protein that reduces cell growth by stimulating apoptosis. Alternative splicing and the use of alternative promoters result in multiple transcript variants encoding the same protein. This gene is imprinted in brain where different transcript variants are expressed from each parental allele. Transcript variants initiating from the upstream promoter are expressed preferentially from the maternal allele, while transcript variants initiating downstream of the interspersed NNAT gene (GeneID:4826) are expressed from the paternal allele. Transcripts at this locus may also undergo A to I editing, resulting in amino acid changes at three positions in the N-terminus of the protein. [provided by RefSeq, Nov 2015]","start":37492472,"end":37527931,"strand":-1,"description":"bladder cancer associated protein [Source:HGNC Symbol;Acc:HGNC:1055]"}, {"versioned_ensembl_gene_id":"ENSG00000281811.1","gene_symbol":"LINC02287","gene_name":"long intergenic non-protein coding RNA 2287 [Source:HGNC Symbol;Acc:HGNC:53204]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929002","summary":null,"start":92905697,"end":92907482,"strand":-1,"description":"long intergenic non-protein coding RNA 2287 [Source:HGNC Symbol;Acc:HGNC:53204]"}, {"versioned_ensembl_gene_id":"ENSG00000271943.1","gene_symbol":"AC098614.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27638315,"end":27638776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171234.13","gene_symbol":"UGT2B7","gene_name":"UDP glucuronosyltransferase family 2 member B7 [Source:HGNC Symbol;Acc:HGNC:12554]","synonyms":"UGT2B9","biotype":"protein_coding","ncbi_id":"7364","summary":"The protein encoded by this gene belongs to the UDP-glycosyltransferase (UGT) family. UGTs serve a major role in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This protein is localized in the microsome membrane, and has unique specificity for 3,4-catechol estrogens and estriol, suggesting that it may play an important role in regulating the level and activity of these potent estrogen metabolites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2017]","start":69051363,"end":69112987,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B7 [Source:HGNC Symbol;Acc:HGNC:12554]"}, {"versioned_ensembl_gene_id":"ENSG00000103043.14","gene_symbol":"VAC14","gene_name":"Vac14, PIKFYVE complex component [Source:HGNC Symbol;Acc:HGNC:25507]","synonyms":"TAX1BP2,FLJ10305,ArPIKfyve","biotype":"protein_coding","ncbi_id":"55697","summary":"This gene encodes a scaffold protein that is a component of the PIKfyve protein kinase complex. This complex is responsible for the synthesis of phosphatidylinositol 3,5-bisphosphate, an important component of cellular membranes, from phosphatidylinositol 3-phosphate. Mice lacking a functional copy of this gene exhibit severe neurodegeneration. Mutations in the human gene have been identified in patients with a childhood onset progressive neurological disorder characterized by impaired movement, dystonia, and striatal abnormalities. [provided by RefSeq, May 2017]","start":70687439,"end":70801161,"strand":-1,"description":"Vac14, PIKFYVE complex component [Source:HGNC Symbol;Acc:HGNC:25507]"}, {"versioned_ensembl_gene_id":"ENSG00000276603.1","gene_symbol":"AL109614.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":37526642,"end":37527060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163017.13","gene_symbol":"ACTG2","gene_name":"actin, gamma 2, smooth muscle, enteric [Source:HGNC Symbol;Acc:HGNC:145]","synonyms":"ACTSG,ACTL3,ACTA3","biotype":"protein_coding","ncbi_id":"72","summary":"Actins are highly conserved proteins that are involved in various types of cell motility and in the maintenance of the cytoskeleton. Three types of actins, alpha, beta and gamma, have been identified in vertebrates. Alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. This gene encodes actin gamma 2; a smooth muscle actin found in enteric tissues. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Based on similarity to peptide cleavage of related actins, the mature protein of this gene is formed by removal of two N-terminal peptides.[provided by RefSeq, Dec 2010]","start":73892314,"end":73919865,"strand":1,"description":"actin, gamma 2, smooth muscle, enteric [Source:HGNC Symbol;Acc:HGNC:145]"}, {"versioned_ensembl_gene_id":"ENSG00000260156.1","gene_symbol":"AC020763.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70747057,"end":70747926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132004.12","gene_symbol":"FBXW9","gene_name":"F-box and WD repeat domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28136]","synonyms":"MGC10870,Fbw9","biotype":"protein_coding","ncbi_id":"84261","summary":"Members of the F-box protein family, such as FBXW9, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":12688053,"end":12696643,"strand":-1,"description":"F-box and WD repeat domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28136]"}, {"versioned_ensembl_gene_id":"ENSG00000278932.3","gene_symbol":"CR381653.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9325013,"end":9368775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267791.1","gene_symbol":"AC018761.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12688922,"end":12689238,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283980.1","gene_symbol":"GNG14","gene_name":"G protein subunit gamma 14 [Source:HGNC Symbol;Acc:HGNC:53439]","synonyms":null,"biotype":"protein_coding","ncbi_id":"105372280","summary":null,"start":12687998,"end":12688422,"strand":1,"description":"G protein subunit gamma 14 [Source:HGNC Symbol;Acc:HGNC:53439]"}, {"versioned_ensembl_gene_id":"ENSG00000104413.15","gene_symbol":"ESRP1","gene_name":"epithelial splicing regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:25966]","synonyms":"RBM35A,FLJ20171","biotype":"protein_coding","ncbi_id":"54845","summary":"ESPR1 is an epithelial cell-type-specific splicing regulator (Warzecha et al., 2009 [PubMed 19285943]).[supplied by OMIM, Aug 2009]","start":94641074,"end":94707466,"strand":1,"description":"epithelial splicing regulatory protein 1 [Source:HGNC Symbol;Acc:HGNC:25966]"}, {"versioned_ensembl_gene_id":"ENSG00000280805.2","gene_symbol":"AL117192.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92886352,"end":92893506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103502.13","gene_symbol":"CDIPT","gene_name":"CDP-diacylglycerol--inositol 3-phosphatidyltransferase [Source:HGNC Symbol;Acc:HGNC:1769]","synonyms":"PIS1,PIS","biotype":"protein_coding","ncbi_id":"10423","summary":"Phosphatidylinositol breakdown products are ubiquitous second messengers that function downstream of many G protein-coupled receptors and tyrosine kinases regulating cell growth, calcium metabolism, and protein kinase C activity. Two enzymes, CDP-diacylglycerol synthase and phosphatidylinositol synthase, are involved in the biosynthesis of phosphatidylinositol. Phosphatidylinositol synthase, a member of the CDP-alcohol phosphatidyl transferase class-I family, is an integral membrane protein found on the cytoplasmic side of the endoplasmic reticulum and the Golgi apparatus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]","start":29858357,"end":29863736,"strand":-1,"description":"CDP-diacylglycerol--inositol 3-phosphatidyltransferase [Source:HGNC Symbol;Acc:HGNC:1769]"}, {"versioned_ensembl_gene_id":"ENSG00000159197.3","gene_symbol":"KCNE2","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:6242]","synonyms":"MiRP1,LQT6","biotype":"protein_coding","ncbi_id":"9992","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a small integral membrane subunit that assembles with the KCNH2 gene product, a pore-forming protein, to alter its function. This gene is expressed in heart and muscle and the gene mutations are associated with cardiac arrhythmia. [provided by RefSeq, Jul 2008]","start":34364024,"end":34371389,"strand":1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:6242]"}, {"versioned_ensembl_gene_id":"ENSG00000248763.2","gene_symbol":"AC111000.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69066395,"end":69069888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225555.1","gene_symbol":"AP000320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34370802,"end":34375348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234386.4","gene_symbol":"OR7E162P","gene_name":"olfactory receptor family 7 subfamily E member 162 pseudogene [Source:HGNC Symbol;Acc:HGNC:28374]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"442101","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":3901566,"end":3902594,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 162 pseudogene [Source:HGNC Symbol;Acc:HGNC:28374]"}, {"versioned_ensembl_gene_id":"ENSG00000278713.1","gene_symbol":"AC120114.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29862760,"end":29863417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284700.1","gene_symbol":"AL049637.2","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":50423609,"end":50425316,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238223.1","gene_symbol":"AL121878.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":115063936,"end":115064794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268945.1","gene_symbol":"AC010422.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12682693,"end":12687279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262938.6","gene_symbol":"C21orf62","gene_name":"chromosome 21 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:1305]","synonyms":"C21orf120,B37,PRED81","biotype":"protein_coding","ncbi_id":"56245","summary":null,"start":32793564,"end":32813728,"strand":-1,"description":"chromosome 21 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:1305]"}, {"versioned_ensembl_gene_id":"ENSG00000053438.8","gene_symbol":"NNAT","gene_name":"neuronatin [Source:HGNC Symbol;Acc:HGNC:7860]","synonyms":"Peg5","biotype":"protein_coding","ncbi_id":"4826","summary":"The protein encoded by this gene is a proteolipid that may be involved in the regulation of ion channels during brain development. The encoded protein may also play a role in forming and maintaining the structure of the nervous system. This gene is found within an intron of another gene, bladder cancer associated protein, but on the opposite strand. This gene is imprinted and is expressed only from the paternal allele. [provided by RefSeq, Apr 2016]","start":37521215,"end":37523693,"strand":1,"description":"neuronatin [Source:HGNC Symbol;Acc:HGNC:7860]"}, {"versioned_ensembl_gene_id":"ENSG00000233929.1","gene_symbol":"MT1XP1","gene_name":"metallothionein 1X pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7442]","synonyms":"MTL1","biotype":"processed_pseudogene","ncbi_id":"645652","summary":null,"start":16241213,"end":16241398,"strand":-1,"description":"metallothionein 1X pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7442]"}, {"versioned_ensembl_gene_id":"ENSG00000251166.1","gene_symbol":"OR7E163P","gene_name":"olfactory receptor family 7 subfamily E member 163 pseudogene [Source:HGNC Symbol;Acc:HGNC:45040]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100131415","summary":null,"start":3889356,"end":3890249,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 163 pseudogene [Source:HGNC Symbol;Acc:HGNC:45040]"}, {"versioned_ensembl_gene_id":"ENSG00000262884.1","gene_symbol":"AC015921.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2962248,"end":2965895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280072.1","gene_symbol":"AP000280.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32790673,"end":32791504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225359.1","gene_symbol":"AL358393.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181190471,"end":181191149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184160.7","gene_symbol":"ADRA2C","gene_name":"adrenoceptor alpha 2C [Source:HGNC Symbol;Acc:HGNC:283]","synonyms":"ADRARL2,ADRA2RL2,ADRA2L2","biotype":"protein_coding","ncbi_id":"152","summary":"Alpha-2-adrenergic receptors are members of the G protein-coupled receptor superfamily. They include 3 highly homologous subtypes: alpha2A, alpha2B, and alpha2C. These receptors have a critical role in regulating neurotransmitter release from sympathetic nerves and from adrenergic neurons in the central nervous system. The mouse studies revealed that both the alpha2A and alpha2C subtypes were required for normal presynaptic control of transmitter release from sympathetic nerves in the heart and from central noradrenergic neurons. The alpha2A subtype inhibited transmitter release at high stimulation frequencies, whereas the alpha2C subtype modulated neurotransmission at lower levels of nerve activity. This gene encodes the alpha2C subtype, which contains no introns in either its coding or untranslated sequences. [provided by RefSeq, Jul 2008]","start":3766348,"end":3768526,"strand":1,"description":"adrenoceptor alpha 2C [Source:HGNC Symbol;Acc:HGNC:283]"}, {"versioned_ensembl_gene_id":"ENSG00000237292.1","gene_symbol":"LINC01732","gene_name":"long intergenic non-protein coding RNA 1732 [Source:HGNC Symbol;Acc:HGNC:52520]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928973","summary":null,"start":181174484,"end":181182208,"strand":1,"description":"long intergenic non-protein coding RNA 1732 [Source:HGNC Symbol;Acc:HGNC:52520]"}, {"versioned_ensembl_gene_id":"ENSG00000230248.1","gene_symbol":"Z98742.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108275642,"end":108276546,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116747.12","gene_symbol":"TROVE2","gene_name":"TROVE domain family member 2 [Source:HGNC Symbol;Acc:HGNC:11313]","synonyms":"SSA2,Ro60","biotype":"protein_coding","ncbi_id":"6738","summary":null,"start":193059422,"end":193091777,"strand":1,"description":"TROVE domain family member 2 [Source:HGNC Symbol;Acc:HGNC:11313]"}, {"versioned_ensembl_gene_id":"ENSG00000226791.6","gene_symbol":"AC109826.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":98761938,"end":98772920,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229863.1","gene_symbol":"AC097358.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57134142,"end":57134723,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253620.2","gene_symbol":"AC144568.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64091,"end":64320,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232475.1","gene_symbol":"HSFY5P","gene_name":"heat shock transcription factor, Y-linked 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38789]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478934","summary":null,"start":22048554,"end":22049347,"strand":-1,"description":"heat shock transcription factor, Y-linked 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:38789]"}, {"versioned_ensembl_gene_id":"ENSG00000260949.1","gene_symbol":"AP006545.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":38062881,"end":38063791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223968.1","gene_symbol":"AC098614.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27624202,"end":27624456,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258712.2","gene_symbol":"AC060814.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21372793,"end":21373881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223475.1","gene_symbol":"AC099681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":55573171,"end":55588336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226908.1","gene_symbol":"HIST1H2BPS3","gene_name":"histone cluster 1 H2B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42633]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100820735","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 13. [provided by RefSeq, Oct 2015]","start":21483834,"end":21484174,"strand":-1,"description":"histone cluster 1 H2B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42633]"}, {"versioned_ensembl_gene_id":"ENSG00000254040.1","gene_symbol":"AC103719.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21023296,"end":21029058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184661.13","gene_symbol":"CDCA2","gene_name":"cell division cycle associated 2 [Source:HGNC Symbol;Acc:HGNC:14623]","synonyms":"Repo-Man,PPP1R81","biotype":"protein_coding","ncbi_id":"157313","summary":"This gene encodes a targeting subunit of the cell-cycle associated protein, protein phosphatase 1, with a role in targeting this protein to chromatin during anaphase. These two proteins comprise a phosphatase complex that is involved in nuclear envelope reformation and regulation of the DNA damage response. The encoded protein may also play a role in cancer progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":25458997,"end":25507920,"strand":1,"description":"cell division cycle associated 2 [Source:HGNC Symbol;Acc:HGNC:14623]"}, {"versioned_ensembl_gene_id":"ENSG00000197990.6","gene_symbol":"ZNF734P","gene_name":"zinc finger protein 734, pseudogene [Source:HGNC Symbol;Acc:HGNC:32465]","synonyms":"ZNF734","biotype":"unprocessed_pseudogene","ncbi_id":"644017","summary":null,"start":63449819,"end":63456687,"strand":1,"description":"zinc finger protein 734, pseudogene [Source:HGNC Symbol;Acc:HGNC:32465]"}, {"versioned_ensembl_gene_id":"ENSG00000254266.5","gene_symbol":"PKIA-AS1","gene_name":"PKIA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51659]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927003","summary":null,"start":78426103,"end":78558503,"strand":-1,"description":"PKIA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51659]"}, {"versioned_ensembl_gene_id":"ENSG00000237208.1","gene_symbol":"AL445072.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":126109762,"end":126115562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000009954.10","gene_symbol":"BAZ1B","gene_name":"bromodomain adjacent to zinc finger domain 1B [Source:HGNC Symbol;Acc:HGNC:961]","synonyms":"WSTF,WBSCR9,WBSCR10","biotype":"protein_coding","ncbi_id":"9031","summary":"This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008]","start":73440398,"end":73522278,"strand":-1,"description":"bromodomain adjacent to zinc finger domain 1B [Source:HGNC Symbol;Acc:HGNC:961]"}, {"versioned_ensembl_gene_id":"ENSG00000131386.17","gene_symbol":"GALNT15","gene_name":"polypeptide N-acetylgalactosaminyltransferase 15 [Source:HGNC Symbol;Acc:HGNC:21531]","synonyms":"pp-GalNAc-T15,GALNTL2,GALNT7","biotype":"protein_coding","ncbi_id":"117248","summary":null,"start":16174649,"end":16231992,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 15 [Source:HGNC Symbol;Acc:HGNC:21531]"}, {"versioned_ensembl_gene_id":"ENSG00000136999.4","gene_symbol":"NOV","gene_name":"nephroblastoma overexpressed [Source:HGNC Symbol;Acc:HGNC:7885]","synonyms":"IGFBP9,CCN3","biotype":"protein_coding","ncbi_id":"4856","summary":"The protein encoded by this gene is a small secreted cysteine-rich protein and a member of the CCN family of regulatory proteins. CNN family proteins associate with the extracellular matrix and play an important role in cardiovascular and skeletal development, fibrosis and cancer development. [provided by RefSeq, Feb 2009]","start":119416306,"end":119424353,"strand":1,"description":"nephroblastoma overexpressed [Source:HGNC Symbol;Acc:HGNC:7885]"}, {"versioned_ensembl_gene_id":"ENSG00000272173.1","gene_symbol":"U47924.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6943508,"end":6944604,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134291.11","gene_symbol":"TMEM106C","gene_name":"transmembrane protein 106C [Source:HGNC Symbol;Acc:HGNC:28775]","synonyms":"MGC5576","biotype":"protein_coding","ncbi_id":"79022","summary":null,"start":47963569,"end":47968878,"strand":1,"description":"transmembrane protein 106C [Source:HGNC Symbol;Acc:HGNC:28775]"}, {"versioned_ensembl_gene_id":"ENSG00000238358.2","gene_symbol":"AC004969.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90119299,"end":90122890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240990.9","gene_symbol":"HOXA11-AS","gene_name":"HOXA11 antisense RNA [Source:HGNC Symbol;Acc:HGNC:24957]","synonyms":"NCRNA00076,HOXA11S,HOXA11AS,HOXA11-AS1,HOXA-AS5","biotype":"antisense_RNA","ncbi_id":"221883","summary":"This gene produces a long non-coding RNA in antisense to transcription of the homeobox A11 gene. This transcript may associate with chromatin factors such as Polycomb repressive complex and act as a sponge for microRNAs, thereby participating in the regulation of expression of target genes. High levels of this transcript may be associated with tumor progression. [provided by RefSeq, Dec 2017]","start":27184518,"end":27189293,"strand":1,"description":"HOXA11 antisense RNA [Source:HGNC Symbol;Acc:HGNC:24957]"}, {"versioned_ensembl_gene_id":"ENSG00000258001.1","gene_symbol":"AC126614.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57431116,"end":57433935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278389.1","gene_symbol":"AC099518.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19111035,"end":19111484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230441.1","gene_symbol":"UBQLN1P1","gene_name":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]","synonyms":"UBQLN1P","biotype":"processed_pseudogene","ncbi_id":"387117","summary":null,"start":30353022,"end":30354190,"strand":-1,"description":"ubiquilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21633]"}, {"versioned_ensembl_gene_id":"ENSG00000262953.1","gene_symbol":"EIF4A1P9","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642746","summary":null,"start":2586330,"end":2587866,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37928]"}, {"versioned_ensembl_gene_id":"ENSG00000254819.1","gene_symbol":"AC021698.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26285711,"end":26288007,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275223.1","gene_symbol":"AL121906.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33655701,"end":33656423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256892.2","gene_symbol":"MTRNR2L7","gene_name":"MT-RNR2-like 7 [Source:HGNC Symbol;Acc:HGNC:37164]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288485","summary":null,"start":37601440,"end":37602974,"strand":-1,"description":"MT-RNR2-like 7 [Source:HGNC Symbol;Acc:HGNC:37164]"}, {"versioned_ensembl_gene_id":"ENSG00000235821.1","gene_symbol":"IFITM4P","gene_name":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]","synonyms":"dJ377H14.5","biotype":"processed_pseudogene","ncbi_id":"340198","summary":null,"start":29750729,"end":29751148,"strand":-1,"description":"interferon induced transmembrane protein 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:21669]"}, {"versioned_ensembl_gene_id":"ENSG00000267201.1","gene_symbol":"LINC01775","gene_name":"long intergenic non-protein coding RNA 1775 [Source:HGNC Symbol;Acc:HGNC:52565]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928602","summary":null,"start":2458935,"end":2462185,"strand":-1,"description":"long intergenic non-protein coding RNA 1775 [Source:HGNC Symbol;Acc:HGNC:52565]"}, {"versioned_ensembl_gene_id":"ENSG00000251074.1","gene_symbol":"AC147055.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68626847,"end":68628899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000091986.15","gene_symbol":"CCDC80","gene_name":"coiled-coil domain containing 80 [Source:HGNC Symbol;Acc:HGNC:30649]","synonyms":"URB,SSG1,DRO1","biotype":"protein_coding","ncbi_id":"151887","summary":null,"start":112596794,"end":112649530,"strand":-1,"description":"coiled-coil domain containing 80 [Source:HGNC Symbol;Acc:HGNC:30649]"}, {"versioned_ensembl_gene_id":"ENSG00000241505.1","gene_symbol":"AL391645.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":190480379,"end":190494297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000161904.11","gene_symbol":"LEMD2","gene_name":"LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21244]","synonyms":"NET25,dJ482C21.1","biotype":"protein_coding","ncbi_id":"221496","summary":"This gene encodes a LEM domain-containing transmembrane protein of the inner nuclear membrane. The protein is involved in nuclear structure organization and plays a role in cell signaling and differentiation. Mutations in this gene result in Cataract 46, juvenile-onset. Multiple transcript variants have been found for this gene. [provided by RefSeq, Feb 2017]","start":33771202,"end":33789136,"strand":-1,"description":"LEM domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21244]"}, {"versioned_ensembl_gene_id":"ENSG00000198015.12","gene_symbol":"MRPL42","gene_name":"mitochondrial ribosomal protein L42 [Source:HGNC Symbol;Acc:HGNC:14493]","synonyms":"HSPC204,RPML31,PTD007,MRPS32,MRPL31,MRP-L31","biotype":"protein_coding","ncbi_id":"28977","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a protein identified as belonging to both the 28S and the 39S subunits. Alternative splicing results in multiple transcript variants. Pseudogenes corresponding to this gene are found on chromosomes 4q, 6p, 6q, 7p, and 15q. [provided by RefSeq, May 2011]","start":93467488,"end":93516213,"strand":1,"description":"mitochondrial ribosomal protein L42 [Source:HGNC Symbol;Acc:HGNC:14493]"}, {"versioned_ensembl_gene_id":"ENSG00000180353.10","gene_symbol":"HCLS1","gene_name":"hematopoietic cell-specific Lyn substrate 1 [Source:HGNC Symbol;Acc:HGNC:4844]","synonyms":"HS1,CTTNL","biotype":"protein_coding","ncbi_id":"3059","summary":null,"start":121631399,"end":121660927,"strand":-1,"description":"hematopoietic cell-specific Lyn substrate 1 [Source:HGNC Symbol;Acc:HGNC:4844]"}, {"versioned_ensembl_gene_id":"ENSG00000226466.2","gene_symbol":"RPA2P2","gene_name":"replication protein A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389990","summary":null,"start":81136540,"end":81137335,"strand":-1,"description":"replication protein A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45117]"}, {"versioned_ensembl_gene_id":"ENSG00000229097.1","gene_symbol":"CALM2P2","gene_name":"calmodulin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1447]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"806","summary":null,"start":70163685,"end":70164124,"strand":1,"description":"calmodulin 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1447]"}, {"versioned_ensembl_gene_id":"ENSG00000187812.12","gene_symbol":"AC019294.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75775553,"end":75786898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204267.13","gene_symbol":"TAP2","gene_name":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]","synonyms":"D6S217E,RING11,ABCB3,PSF2","biotype":"protein_coding","ncbi_id":"6891","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]","start":32821833,"end":32838780,"strand":-1,"description":"transporter 2, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:44]"}, {"versioned_ensembl_gene_id":"ENSG00000149541.9","gene_symbol":"B3GAT3","gene_name":"beta-1,3-glucuronyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:923]","synonyms":"GlcAT-I","biotype":"protein_coding","ncbi_id":"26229","summary":"The protein encoded by this gene is a member of the glucuronyltransferase gene family, enzymes that exhibit strict acceptor specificity, recognizing nonreducing terminal sugars and their anomeric linkages. This gene product catalyzes the formation of the glycosaminoglycan-protein linkage by way of a glucuronyl transfer reaction in the final step of the biosynthesis of the linkage region of proteoglycans. A pseudogene of this gene has been identified on chromosome 3. [provided by RefSeq, Dec 2013]","start":62615296,"end":62622175,"strand":-1,"description":"beta-1,3-glucuronyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:923]"}, {"versioned_ensembl_gene_id":"ENSG00000279614.1","gene_symbol":"AC092364.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21809967,"end":21810673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105664.10","gene_symbol":"COMP","gene_name":"cartilage oligomeric matrix protein [Source:HGNC Symbol;Acc:HGNC:2227]","synonyms":"THBS5,PSACH,MED,EPD1,EDM1","biotype":"protein_coding","ncbi_id":"1311","summary":"The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq, Jul 2016]","start":18782773,"end":18791314,"strand":-1,"description":"cartilage oligomeric matrix protein [Source:HGNC Symbol;Acc:HGNC:2227]"}, {"versioned_ensembl_gene_id":"ENSG00000136381.12","gene_symbol":"IREB2","gene_name":"iron responsive element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6115]","synonyms":"IRP2","biotype":"protein_coding","ncbi_id":"3658","summary":"The protein encoded by this gene is an RNA-binding protein that acts to regulate iron levels in the cells by regulating the translation and stability of mRNAs that affect iron homeostasis under conditions when iron is depleted. When iron levels are low, this protein binds to iron-responsive elements (IRES), stem-loop structures located either in the 5' or 3' UTRs. Binding to the 5' UTR represses translation, while binding to the 3' UTR inhibits mRNA degradation. When iron is found in the cell, this protein is degraded in a F-box and leucine rich repeat protein 5-dependent manner. Variants in this gene have been associated with lung cancer and chronic obstructive pulmonary disease (COPD). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]","start":78437431,"end":78501456,"strand":1,"description":"iron responsive element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6115]"}, {"versioned_ensembl_gene_id":"ENSG00000259945.1","gene_symbol":"AC027682.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67542123,"end":67542963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174292.12","gene_symbol":"TNK1","gene_name":"tyrosine kinase non receptor 1 [Source:HGNC Symbol;Acc:HGNC:11940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8711","summary":"The protein encoded by this gene belongs to the tyrosine protein kinase family. Tyrosine protein kinases are important regulators of intracellular signal transduction pathways, mediating cellular proliferation, survival, and development. This gene is highly expressed in fetal tissues and at lower levels in few adult tissues, thus may function in signaling pathways utilized broadly during fetal development, and more selectively in adult tissues. It plays a negative regulatory role in the Ras-Raf1-MAPK pathway, and knockout mice have been shown to develop spontaneous tumors, suggesting a role as a tumor suppressor gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":7380534,"end":7389774,"strand":1,"description":"tyrosine kinase non receptor 1 [Source:HGNC Symbol;Acc:HGNC:11940]"}, {"versioned_ensembl_gene_id":"ENSG00000131584.18","gene_symbol":"ACAP3","gene_name":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 [Source:HGNC Symbol;Acc:HGNC:16754]","synonyms":"KIAA1716,CENTB5","biotype":"protein_coding","ncbi_id":"116983","summary":null,"start":1292376,"end":1309609,"strand":-1,"description":"ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 [Source:HGNC Symbol;Acc:HGNC:16754]"}, {"versioned_ensembl_gene_id":"ENSG00000254836.1","gene_symbol":"AL035078.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32052843,"end":32053260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237457.6","gene_symbol":"LINC01351","gene_name":"long intergenic non-protein coding RNA 1351 [Source:HGNC Symbol;Acc:HGNC:50577]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929120","summary":null,"start":190478551,"end":190480735,"strand":1,"description":"long intergenic non-protein coding RNA 1351 [Source:HGNC Symbol;Acc:HGNC:50577]"}, {"versioned_ensembl_gene_id":"ENSG00000272128.1","gene_symbol":"AP006545.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38099471,"end":38099931,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235436.10","gene_symbol":"DPY19L2P4","gene_name":"DPY19L2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:22176]","synonyms":"IMAGE:5295327","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"442523","summary":null,"start":90119400,"end":90125600,"strand":1,"description":"DPY19L2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:22176]"}, {"versioned_ensembl_gene_id":"ENSG00000226041.1","gene_symbol":"AC010745.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16202430,"end":16204226,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228061.5","gene_symbol":"AC131571.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31637328,"end":31767953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253396.1","gene_symbol":"AC016868.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41435298,"end":41440419,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253896.3","gene_symbol":"AC144568.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72601,"end":79775,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079332.14","gene_symbol":"SAR1A","gene_name":"secretion associated Ras related GTPase 1A [Source:HGNC Symbol;Acc:HGNC:10534]","synonyms":"SARA1,Sara,SAR1","biotype":"protein_coding","ncbi_id":"56681","summary":null,"start":70147289,"end":70170523,"strand":-1,"description":"secretion associated Ras related GTPase 1A [Source:HGNC Symbol;Acc:HGNC:10534]"}, {"versioned_ensembl_gene_id":"ENSG00000213846.5","gene_symbol":"AC098614.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":27632976,"end":27635427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272236.1","gene_symbol":"AL645939.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29751965,"end":29752207,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261405.2","gene_symbol":"AC136944.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33562649,"end":33570935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230132.1","gene_symbol":"AC006457.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63480598,"end":63480989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243417.1","gene_symbol":"AC023424.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152551277,"end":152552364,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271578.1","gene_symbol":"AC119501.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101190520,"end":101190994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229553.1","gene_symbol":"USP9YP17","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38753]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480714","summary":null,"start":22049755,"end":22058113,"strand":-1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38753]"}, {"versioned_ensembl_gene_id":"ENSG00000240669.1","gene_symbol":"AC023424.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152613875,"end":152614333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280271.1","gene_symbol":"AC092364.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21778251,"end":21803339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000039523.19","gene_symbol":"RIPOR1","gene_name":"RHO family interacting cell polarization regulator 1 [Source:HGNC Symbol;Acc:HGNC:25836]","synonyms":"FLJ13725,FAM65A","biotype":"protein_coding","ncbi_id":"79567","summary":null,"start":67518418,"end":67546788,"strand":1,"description":"RHO family interacting cell polarization regulator 1 [Source:HGNC Symbol;Acc:HGNC:25836]"}, {"versioned_ensembl_gene_id":"ENSG00000175189.3","gene_symbol":"INHBC","gene_name":"inhibin beta C subunit [Source:HGNC Symbol;Acc:HGNC:6068]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3626","summary":"This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate a subunit of homodimeric and heterodimeric activin complexes. The heterodimeric complex may function in the inhibition of activin A signaling. Transgenic mice overexpressing this gene exhibit defects in testis, liver and prostate. [provided by RefSeq, Aug 2016]","start":57434760,"end":57450828,"strand":1,"description":"inhibin beta C subunit [Source:HGNC Symbol;Acc:HGNC:6068]"}, {"versioned_ensembl_gene_id":"ENSG00000270896.1","gene_symbol":"AL645939.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29763258,"end":29763392,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198354.6","gene_symbol":"DCAF12L2","gene_name":"DDB1 and CUL4 associated factor 12 like 2 [Source:HGNC Symbol;Acc:HGNC:32950]","synonyms":"WDR40C","biotype":"protein_coding","ncbi_id":"340578","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multi-protein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 9. However, the CDS of this intronless gene remains intact, it is conserved in other mammalian species, it is known to be transcribed, and it is therefore thought to encode a functional protein. [provided by RefSeq, May 2010]","start":126163499,"end":126166097,"strand":-1,"description":"DDB1 and CUL4 associated factor 12 like 2 [Source:HGNC Symbol;Acc:HGNC:32950]"}, {"versioned_ensembl_gene_id":"ENSG00000164740.5","gene_symbol":"SEPT7P5","gene_name":"septin 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38041]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418718","summary":null,"start":63495799,"end":63502536,"strand":1,"description":"septin 7 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38041]"}, {"versioned_ensembl_gene_id":"ENSG00000258767.1","gene_symbol":"AC060814.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21382383,"end":21382842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111676.14","gene_symbol":"ATN1","gene_name":"atrophin 1 [Source:HGNC Symbol;Acc:HGNC:3033]","synonyms":"DRPLA,D12S755E,B37","biotype":"protein_coding","ncbi_id":"1822","summary":"Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein. [provided by RefSeq, Jul 2016]","start":6924463,"end":6942321,"strand":1,"description":"atrophin 1 [Source:HGNC Symbol;Acc:HGNC:3033]"}, {"versioned_ensembl_gene_id":"ENSG00000157214.13","gene_symbol":"STEAP2","gene_name":"STEAP2 metalloreductase [Source:HGNC Symbol;Acc:HGNC:17885]","synonyms":"STMP,STAMP1,PCANAP1,IPCA-1","biotype":"protein_coding","ncbi_id":"261729","summary":"This gene is a member of the STEAP family and encodes a multi-pass membrane protein that localizes to the Golgi complex, the plasma membrane, and the vesicular tubular structures in the cytosol. A highly similar protein in mouse has both ferrireductase and cupric reductase activity, and stimulates the cellular uptake of both iron and copper in vitro. Increased transcriptional expression of the human gene is associated with prostate cancer progression. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":90167590,"end":90238137,"strand":1,"description":"STEAP2 metalloreductase [Source:HGNC Symbol;Acc:HGNC:17885]"}, {"versioned_ensembl_gene_id":"ENSG00000225938.1","gene_symbol":"AL109741.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":101235683,"end":101236528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228876.1","gene_symbol":"AC010745.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16224047,"end":16229140,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272398.5","gene_symbol":"CD24","gene_name":"CD24 molecule [Source:HGNC Symbol;Acc:HGNC:1645]","synonyms":"CD24A","biotype":"protein_coding","ncbi_id":"100133941","summary":"This gene encodes a sialoglycoprotein that is expressed on mature granulocytes and B cells and modulates growth and differentiation signals to these cells. The precursor protein is cleaved to a short 32 amino acid mature peptide which is anchored via a glycosyl phosphatidylinositol (GPI) link to the cell surface. This gene was missing from previous genome assemblies, but is properly located on chromosome 6. Non-transcribed pseudogenes have been designated on chromosomes 1, 15, 20, and Y. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":106969831,"end":106975627,"strand":-1,"description":"CD24 molecule [Source:HGNC Symbol;Acc:HGNC:1645]"}, {"versioned_ensembl_gene_id":"ENSG00000214745.2","gene_symbol":"AL391419.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55961208,"end":55962482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254193.1","gene_symbol":"AC131281.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150584,"end":150728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282086.1","gene_symbol":"PKD1P6","gene_name":"polycystin 1, transient receptor potential channel interacting pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30070]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"353511","summary":null,"start":14952495,"end":14992495,"strand":1,"description":"polycystin 1, transient receptor potential channel interacting pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:30070]"}, {"versioned_ensembl_gene_id":"ENSG00000227486.1","gene_symbol":"AL445472.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55908123,"end":56015173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232766.1","gene_symbol":"AC098614.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27703129,"end":27703568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168778.11","gene_symbol":"TCTN2","gene_name":"tectonic family member 2 [Source:HGNC Symbol;Acc:HGNC:25774]","synonyms":"C12orf38,TECT2,MKS8,JBTS24,FLJ12975","biotype":"protein_coding","ncbi_id":"79867","summary":"This gene encodes a type I membrane protein that belongs to the tectonic family. Studies in mice suggest that this protein may be involved in hedgehog signaling, and essential for ciliogenesis. Mutations in this gene are associated with Meckel syndrome type 8. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":123671113,"end":123708403,"strand":1,"description":"tectonic family member 2 [Source:HGNC Symbol;Acc:HGNC:25774]"}, {"versioned_ensembl_gene_id":"ENSG00000253612.1","gene_symbol":"WBP1LP3","gene_name":"WW domain binding protein 1-like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43958]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479031","summary":null,"start":155274,"end":155481,"strand":1,"description":"WW domain binding protein 1-like pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43958]"}, {"versioned_ensembl_gene_id":"ENSG00000272282.1","gene_symbol":"LINC02084","gene_name":"long intergenic non-protein coding RNA 2084 [Source:HGNC Symbol;Acc:HGNC:52934]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377006","summary":null,"start":27712910,"end":27714005,"strand":1,"description":"long intergenic non-protein coding RNA 2084 [Source:HGNC Symbol;Acc:HGNC:52934]"}, {"versioned_ensembl_gene_id":"ENSG00000162882.14","gene_symbol":"HAAO","gene_name":"3-hydroxyanthranilate 3,4-dioxygenase [Source:HGNC Symbol;Acc:HGNC:4796]","synonyms":null,"biotype":"protein_coding","ncbi_id":"23498","summary":"3-Hydroxyanthranilate 3,4-dioxygenase is a monomeric cytosolic protein belonging to the family of intramolecular dioxygenases containing nonheme ferrous iron. It is widely distributed in peripheral organs, such as liver and kidney, and is also present in low amounts in the central nervous system. HAAO catalyzes the synthesis of quinolinic acid (QUIN) from 3-hydroxyanthranilic acid. QUIN is an excitotoxin whose toxicity is mediated by its ability to activate glutamate N-methyl-D-aspartate receptors. Increased cerebral levels of QUIN may participate in the pathogenesis of neurologic and inflammatory disorders. HAAO has been suggested to play a role in disorders associated with altered tissue levels of QUIN. [provided by RefSeq, Jul 2008]","start":42767089,"end":42792593,"strand":-1,"description":"3-hydroxyanthranilate 3,4-dioxygenase [Source:HGNC Symbol;Acc:HGNC:4796]"}, {"versioned_ensembl_gene_id":"ENSG00000236674.1","gene_symbol":"AL049636.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63359823,"end":63361179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231266.1","gene_symbol":"AC010745.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16227027,"end":16228194,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266338.6","gene_symbol":"NBPF15","gene_name":"NBPF member 15 [Source:HGNC Symbol;Acc:HGNC:28791]","synonyms":"NBPF16,MGC8902","biotype":"protein_coding","ncbi_id":"284565","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013]","start":144421386,"end":144461674,"strand":-1,"description":"NBPF member 15 [Source:HGNC Symbol;Acc:HGNC:28791]"}, {"versioned_ensembl_gene_id":"ENSG00000176269.3","gene_symbol":"OR4F21","gene_name":"olfactory receptor family 4 subfamily F member 21 [Source:HGNC Symbol;Acc:HGNC:19583]","synonyms":"OR4F21P","biotype":"protein_coding","ncbi_id":"441308","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":166049,"end":167043,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 21 [Source:HGNC Symbol;Acc:HGNC:19583]"}, {"versioned_ensembl_gene_id":"ENSG00000231552.1","gene_symbol":"IGBP1P3","gene_name":"immunoglobulin (CD79A) binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43612]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391526","summary":null,"start":32620903,"end":32621902,"strand":-1,"description":"immunoglobulin (CD79A) binding protein 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43612]"}, {"versioned_ensembl_gene_id":"ENSG00000197992.6","gene_symbol":"CLEC9A","gene_name":"C-type lectin domain containing 9A [Source:HGNC Symbol;Acc:HGNC:26705]","synonyms":"UNQ9341,HEEE9341,DNGR-1,CD370","biotype":"protein_coding","ncbi_id":"283420","summary":"CLEC9A is a group V C-type lectin-like receptor (CTLR) that functions as an activation receptor and is expressed on myeloid lineage cells (Huysamen et al., 2008 [PubMed 18408006]).[supplied by OMIM, Aug 2008]","start":10030677,"end":10066027,"strand":1,"description":"C-type lectin domain containing 9A [Source:HGNC Symbol;Acc:HGNC:26705]"}, {"versioned_ensembl_gene_id":"ENSG00000228645.2","gene_symbol":"PHKG1P2","gene_name":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33917]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644032","summary":null,"start":63509303,"end":63510165,"strand":1,"description":"phosphorylase kinase catalytic subunit gamma 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33917]"}, {"versioned_ensembl_gene_id":"ENSG00000255252.3","gene_symbol":"AL078612.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32097143,"end":32105091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258848.1","gene_symbol":"GRAMD4P6","gene_name":"GRAM domain containing 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100631250","summary":null,"start":21383821,"end":21384064,"strand":1,"description":"GRAM domain containing 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49141]"}, {"versioned_ensembl_gene_id":"ENSG00000171033.12","gene_symbol":"PKIA","gene_name":"cAMP-dependent protein kinase inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:9017]","synonyms":"PRKACN1","biotype":"protein_coding","ncbi_id":"5569","summary":"The protein encoded by this gene is a member of the cAMP-dependent protein kinase (PKA) inhibitor family. This protein was demonstrated to interact with and inhibit the activities of both C alpha and C beta catalytic subunits of the PKA. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]","start":78516139,"end":78605267,"strand":1,"description":"cAMP-dependent protein kinase inhibitor alpha [Source:HGNC Symbol;Acc:HGNC:9017]"}, {"versioned_ensembl_gene_id":"ENSG00000255490.1","gene_symbol":"EIF4A2P5","gene_name":"eukaryotic translation initiation factor 4A2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45102]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480446","summary":null,"start":32085111,"end":32085712,"strand":1,"description":"eukaryotic translation initiation factor 4A2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45102]"}, {"versioned_ensembl_gene_id":"ENSG00000232444.1","gene_symbol":"AC010745.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16316324,"end":16319566,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255464.1","gene_symbol":"SEPT14P8","gene_name":"septin 14 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51692]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480341","summary":null,"start":200385,"end":200562,"strand":-1,"description":"septin 14 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51692]"}, {"versioned_ensembl_gene_id":"ENSG00000136244.11","gene_symbol":"IL6","gene_name":"interleukin 6 [Source:HGNC Symbol;Acc:HGNC:6018]","synonyms":"IL-6,IFNB2,HSF,HGF,BSF2","biotype":"protein_coding","ncbi_id":"3569","summary":"This gene encodes a cytokine that functions in inflammation and the maturation of B cells. In addition, the encoded protein has been shown to be an endogenous pyrogen capable of inducing fever in people with autoimmune diseases or infections. The protein is primarily produced at sites of acute and chronic inflammation, where it is secreted into the serum and induces a transcriptional inflammatory response through interleukin 6 receptor, alpha. The functioning of this gene is implicated in a wide variety of inflammation-associated disease states, including suspectibility to diabetes mellitus and systemic juvenile rheumatoid arthritis. Elevated levels of the encoded protein have been found in virus infections, including COVID-19 (disease caused by SARS-CoV-2). [provided by RefSeq, Aug 2020]","start":22725884,"end":22732002,"strand":1,"description":"interleukin 6 [Source:HGNC Symbol;Acc:HGNC:6018]"}, {"versioned_ensembl_gene_id":"ENSG00000005073.5","gene_symbol":"HOXA11","gene_name":"homeobox A11 [Source:HGNC Symbol;Acc:HGNC:5101]","synonyms":"HOX1,HOX1I","biotype":"protein_coding","ncbi_id":"3207","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia. [provided by RefSeq, Jul 2008]","start":27181510,"end":27185223,"strand":-1,"description":"homeobox A11 [Source:HGNC Symbol;Acc:HGNC:5101]"}, {"versioned_ensembl_gene_id":"ENSG00000254627.1","gene_symbol":"AL035078.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32064912,"end":32072173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253166.2","gene_symbol":"AC131281.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":202660,"end":202897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101337.15","gene_symbol":"TM9SF4","gene_name":"transmembrane 9 superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:30797]","synonyms":"KIAA0255,dJ836N17.2","biotype":"protein_coding","ncbi_id":"9777","summary":null,"start":32109506,"end":32167258,"strand":1,"description":"transmembrane 9 superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:30797]"}, {"versioned_ensembl_gene_id":"ENSG00000224400.5","gene_symbol":"AC010880.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16354256,"end":16432702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160194.17","gene_symbol":"NDUFV3","gene_name":"NADH:ubiquinone oxidoreductase subunit V3 [Source:HGNC Symbol;Acc:HGNC:7719]","synonyms":"CI-10k","biotype":"protein_coding","ncbi_id":"4731","summary":"The protein encoded by this gene is one of at least forty-one subunits that make up the NADH-ubiquinone oxidoreductase complex. This complex is part of the mitochondrial respiratory chain and serves to catalyze the rotenone-sensitive oxidation of NADH and the reduction of ubiquinone. The encoded protein is one of three proteins found in the flavoprotein fraction of the complex. The specific function of the encoded protein is unknown. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":42879644,"end":42913304,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit V3 [Source:HGNC Symbol;Acc:HGNC:7719]"}, {"versioned_ensembl_gene_id":"ENSG00000267480.1","gene_symbol":"AP001542.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":12031178,"end":12032181,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253398.1","gene_symbol":"AC021733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119419910,"end":119462350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106571.12","gene_symbol":"GLI3","gene_name":"GLI family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:4319]","synonyms":"PAP-A,GCPS,ACLS,PPDIV,PHS,PAPB,PAPA1,PAPA","biotype":"protein_coding","ncbi_id":"2737","summary":"This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008]","start":41960950,"end":42237870,"strand":-1,"description":"GLI family zinc finger 3 [Source:HGNC Symbol;Acc:HGNC:4319]"}, {"versioned_ensembl_gene_id":"ENSG00000253508.1","gene_symbol":"AC004080.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27186573,"end":27193448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134339.8","gene_symbol":"SAA2","gene_name":"serum amyloid A2 [Source:HGNC Symbol;Acc:HGNC:10514]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6289","summary":"This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. [provided by RefSeq, Jul 2020]","start":18239223,"end":18248643,"strand":-1,"description":"serum amyloid A2 [Source:HGNC Symbol;Acc:HGNC:10514]"}, {"versioned_ensembl_gene_id":"ENSG00000232177.1","gene_symbol":"MTND4P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42220]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873254","summary":null,"start":126472885,"end":126473281,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42220]"}, {"versioned_ensembl_gene_id":"ENSG00000120659.14","gene_symbol":"TNFSF11","gene_name":"TNF superfamily member 11 [Source:HGNC Symbol;Acc:HGNC:11926]","synonyms":"TRANCE,RANKL,OPGL,ODF,CD254","biotype":"protein_coding","ncbi_id":"8600","summary":"This gene encodes a member of the tumor necrosis factor (TNF) cytokine family which is a ligand for osteoprotegerin and functions as a key factor for osteoclast differentiation and activation. This protein was shown to be a dentritic cell survival factor and is involved in the regulation of T cell-dependent immune response. T cell activation was reported to induce expression of this gene and lead to an increase of osteoclastogenesis and bone loss. This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor-associated factor (TRAF) 6, which indicated this protein may have a role in the regulation of cell apoptosis. Targeted disruption of the related gene in mice led to severe osteopetrosis and a lack of osteoclasts. The deficient mice exhibited defects in early differentiation of T and B lymphocytes, and failed to form lobulo-alveolar mammary structures during pregnancy. Two alternatively spliced transcript variants have been found. [provided by RefSeq, Jul 2008]","start":42562736,"end":42608013,"strand":1,"description":"TNF superfamily member 11 [Source:HGNC Symbol;Acc:HGNC:11926]"}, {"versioned_ensembl_gene_id":"ENSG00000198105.13","gene_symbol":"ZNF248","gene_name":"zinc finger protein 248 [Source:HGNC Symbol;Acc:HGNC:13041]","synonyms":"bA162G10.3","biotype":"protein_coding","ncbi_id":"57209","summary":null,"start":37776526,"end":37858106,"strand":-1,"description":"zinc finger protein 248 [Source:HGNC Symbol;Acc:HGNC:13041]"}, {"versioned_ensembl_gene_id":"ENSG00000256626.1","gene_symbol":"AC024224.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":10040848,"end":10045711,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234267.3","gene_symbol":"TULP3P1","gene_name":"tubby like protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39262]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100128017","summary":null,"start":96941281,"end":96984172,"strand":-1,"description":"tubby like protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39262]"}, {"versioned_ensembl_gene_id":"ENSG00000233977.1","gene_symbol":"AC099681.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55592074,"end":55593193,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072657.8","gene_symbol":"TRHDE","gene_name":"thyrotropin releasing hormone degrading enzyme [Source:HGNC Symbol;Acc:HGNC:30748]","synonyms":"TRH-DE,PGPEP2,PAP-II","biotype":"protein_coding","ncbi_id":"29953","summary":"This gene encodes a member of the peptidase M1 family. The encoded protein is an extracellular peptidase that specifically cleaves and inactivates the neuropeptide thyrotropin-releasing hormone.[provided by RefSeq, Dec 2008]","start":72087266,"end":72670757,"strand":1,"description":"thyrotropin releasing hormone degrading enzyme [Source:HGNC Symbol;Acc:HGNC:30748]"}, {"versioned_ensembl_gene_id":"ENSG00000231394.1","gene_symbol":"AC099681.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":55593777,"end":55595006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261427.6","gene_symbol":"AC099518.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":19114002,"end":19173578,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007372.21","gene_symbol":"PAX6","gene_name":"paired box 6 [Source:HGNC Symbol;Acc:HGNC:8620]","synonyms":"WAGR,D11S812E,AN2,AN","biotype":"protein_coding","ncbi_id":"5080","summary":"This gene encodes paired box protein Pax-6, one of many human homologs of the Drosophila melanogaster gene prd. In addition to a conserved paired box domain, a hallmark feature of this gene family, the encoded protein also contains a homeobox domain. Both domains are known to bind DNA and function as regulators of gene transcription. Activity of this protein is key in the development of neural tissues, particularly the eye. This gene is regulated by multiple enhancers located up to hundreds of kilobases distant from this locus. Mutations in this gene or in the enhancer regions can cause ocular disorders such as aniridia and Peter's anomaly. Use of alternate promoters and alternative splicing results in multiple transcript variants encoding different isoforms. Interestingly, inclusion of a particular alternate coding exon has been shown to increase the length of the paired box domain and alter its DNA binding specificity. Consequently, isoforms that carry the shorter paired box domain regulate a different set of genes compared to the isoforms carrying the longer paired box domain. [provided by RefSeq, Mar 2019]","start":31784779,"end":31818062,"strand":-1,"description":"paired box 6 [Source:HGNC Symbol;Acc:HGNC:8620]"}, {"versioned_ensembl_gene_id":"ENSG00000234844.1","gene_symbol":"CDC42P2","gene_name":"cell division cycle 42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33952]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643336","summary":null,"start":55638274,"end":55638842,"strand":-1,"description":"cell division cycle 42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33952]"}, {"versioned_ensembl_gene_id":"ENSG00000161179.13","gene_symbol":"YDJC","gene_name":"YdjC chitooligosaccharide deacetylase homolog [Source:HGNC Symbol;Acc:HGNC:27158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150223","summary":null,"start":21628089,"end":21630064,"strand":-1,"description":"YdjC chitooligosaccharide deacetylase homolog [Source:HGNC Symbol;Acc:HGNC:27158]"}, {"versioned_ensembl_gene_id":"ENSG00000196620.9","gene_symbol":"UGT2B15","gene_name":"UDP glucuronosyltransferase family 2 member B15 [Source:HGNC Symbol;Acc:HGNC:12546]","synonyms":"UGT2B8","biotype":"protein_coding","ncbi_id":"7366","summary":"This gene encodes a glycosyltransferase that is invovled in the metabolism and elimination of toxic compounts, both endogenous and of xenobiotic origin. This gene plays a role in the regulation of estrogens and androgens. This locus is present in a cluster of similar genes and pseudogenes on chromosome 4. [provided by RefSeq, Aug 2016]","start":68646630,"end":68670628,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B15 [Source:HGNC Symbol;Acc:HGNC:12546]"}, {"versioned_ensembl_gene_id":"ENSG00000272329.1","gene_symbol":"AL353581.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":96948018,"end":96949584,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278522.4","gene_symbol":"POTEB3","gene_name":"POTE ankyrin domain family member B3 [Source:HGNC Symbol;Acc:HGNC:51240]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102724631","summary":null,"start":21408243,"end":21440451,"strand":-1,"description":"POTE ankyrin domain family member B3 [Source:HGNC Symbol;Acc:HGNC:51240]"}, {"versioned_ensembl_gene_id":"ENSG00000261759.1","gene_symbol":"AC099518.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19119976,"end":19121629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180730.4","gene_symbol":"SHISA2","gene_name":"shisa family member 2 [Source:HGNC Symbol;Acc:HGNC:20366]","synonyms":"WGAR9166,TMEM46,PRO28631,hShisa,C13orf13,bA398O19.2","biotype":"protein_coding","ncbi_id":"387914","summary":null,"start":26044597,"end":26051031,"strand":-1,"description":"shisa family member 2 [Source:HGNC Symbol;Acc:HGNC:20366]"}, {"versioned_ensembl_gene_id":"ENSG00000103528.16","gene_symbol":"SYT17","gene_name":"synaptotagmin 17 [Source:HGNC Symbol;Acc:HGNC:24119]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51760","summary":null,"start":19167971,"end":19268334,"strand":1,"description":"synaptotagmin 17 [Source:HGNC Symbol;Acc:HGNC:24119]"}, {"versioned_ensembl_gene_id":"ENSG00000223508.5","gene_symbol":"RPL23AP53","gene_name":"ribosomal protein L23a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:35921]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"644128","summary":null,"start":213186,"end":232231,"strand":-1,"description":"ribosomal protein L23a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:35921]"}, {"versioned_ensembl_gene_id":"ENSG00000137204.14","gene_symbol":"SLC22A7","gene_name":"solute carrier family 22 member 7 [Source:HGNC Symbol;Acc:HGNC:10971]","synonyms":"OAT2,NLT","biotype":"protein_coding","ncbi_id":"10864","summary":"The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":43295694,"end":43305538,"strand":1,"description":"solute carrier family 22 member 7 [Source:HGNC Symbol;Acc:HGNC:10971]"}, {"versioned_ensembl_gene_id":"ENSG00000231393.1","gene_symbol":"AL357874.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35642514,"end":35643517,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137101.12","gene_symbol":"CD72","gene_name":"CD72 molecule [Source:HGNC Symbol;Acc:HGNC:1696]","synonyms":"LYB2,CD72b","biotype":"protein_coding","ncbi_id":"971","summary":null,"start":35609533,"end":35646810,"strand":-1,"description":"CD72 molecule [Source:HGNC Symbol;Acc:HGNC:1696]"}, {"versioned_ensembl_gene_id":"ENSG00000254104.2","gene_symbol":"AC136777.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":264315,"end":264672,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282091.1","gene_symbol":"AC243651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14987680,"end":15002408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272240.1","gene_symbol":"AC004908.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":234347,"end":234887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172748.13","gene_symbol":"ZNF596","gene_name":"zinc finger protein 596 [Source:HGNC Symbol;Acc:HGNC:27268]","synonyms":null,"biotype":"protein_coding","ncbi_id":"169270","summary":null,"start":232137,"end":264703,"strand":1,"description":"zinc finger protein 596 [Source:HGNC Symbol;Acc:HGNC:27268]"}, {"versioned_ensembl_gene_id":"ENSG00000235944.8","gene_symbol":"ZNF815P","gene_name":"zinc finger protein 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:22029]","synonyms":"ZNF815,FLJ38969","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"401303","summary":null,"start":5823160,"end":5854365,"strand":1,"description":"zinc finger protein 815, pseudogene [Source:HGNC Symbol;Acc:HGNC:22029]"}, {"versioned_ensembl_gene_id":"ENSG00000130299.16","gene_symbol":"GTPBP3","gene_name":"GTP binding protein 3 (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:14880]","synonyms":"THDF1,MTGP1,MSS1,GTPBG3,FLJ14700","biotype":"protein_coding","ncbi_id":"84705","summary":"This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Sep 2010]","start":17334920,"end":17342735,"strand":1,"description":"GTP binding protein 3 (mitochondrial) [Source:HGNC Symbol;Acc:HGNC:14880]"}, {"versioned_ensembl_gene_id":"ENSG00000114270.17","gene_symbol":"COL7A1","gene_name":"collagen type VII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2214]","synonyms":"EBD1,EBR1,EBDCT","biotype":"protein_coding","ncbi_id":"1294","summary":"This gene encodes the alpha chain of type VII collagen. The type VII collagen fibril, composed of three identical alpha collagen chains, is restricted to the basement zone beneath stratified squamous epithelia. It functions as an anchoring fibril between the external epithelia and the underlying stroma. Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa. In the absence of mutations, however, an acquired form of this disease can result from an autoimmune response made to type VII collagen. [provided by RefSeq, Jul 2008]","start":48564073,"end":48595267,"strand":-1,"description":"collagen type VII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2214]"}, {"versioned_ensembl_gene_id":"ENSG00000279345.1","gene_symbol":"Z98885.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49805452,"end":49807208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100425.18","gene_symbol":"BRD1","gene_name":"bromodomain containing 1 [Source:HGNC Symbol;Acc:HGNC:1102]","synonyms":"BRPF2,BRL","biotype":"protein_coding","ncbi_id":"23774","summary":"This gene encodes a bromodomain-containing protein that localizes to the nucleus and can interact with DNA and histone tails. The encoded protein is a component of the MOZ/MORF acetyltransferase complex and can stimulate acetylation of histones H3 and H4, thereby potentially playing a role in gene activation. Variation in this gene is associated with schizophrenia and bipolar disorder in some study populations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2017]","start":49773283,"end":49827512,"strand":-1,"description":"bromodomain containing 1 [Source:HGNC Symbol;Acc:HGNC:1102]"}, {"versioned_ensembl_gene_id":"ENSG00000241738.1","gene_symbol":"ZNF90P1","gene_name":"zinc finger protein 90 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12888]","synonyms":"ZNF108P,ZNF108","biotype":"processed_pseudogene","ncbi_id":"7661","summary":null,"start":101357292,"end":101359242,"strand":1,"description":"zinc finger protein 90 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12888]"}, {"versioned_ensembl_gene_id":"ENSG00000282978.1","gene_symbol":"AC110994.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101457241,"end":101457732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188257.10","gene_symbol":"PLA2G2A","gene_name":"phospholipase A2 group IIA [Source:HGNC Symbol;Acc:HGNC:9031]","synonyms":"PLA2L,PLA2B","biotype":"protein_coding","ncbi_id":"5320","summary":"The protein encoded by this gene is a member of the phospholipase A2 family (PLA2). PLA2s constitute a diverse family of enzymes with respect to sequence, function, localization, and divalent cation requirements. This gene product belongs to group II, which contains secreted form of PLA2, an extracellular enzyme that has a low molecular mass and requires calcium ions for catalysis. It catalyzes the hydrolysis of the sn-2 fatty acid acyl ester bond of phosphoglycerides, releasing free fatty acids and lysophospholipids, and thought to participate in the regulation of the phospholipid metabolism in biomembranes. Several alternatively spliced transcript variants with different 5' UTRs have been found for this gene.[provided by RefSeq, Sep 2009]","start":19975431,"end":19980416,"strand":-1,"description":"phospholipase A2 group IIA [Source:HGNC Symbol;Acc:HGNC:9031]"}, {"versioned_ensembl_gene_id":"ENSG00000138468.15","gene_symbol":"SENP7","gene_name":"SUMO1/sentrin specific peptidase 7 [Source:HGNC Symbol;Acc:HGNC:30402]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57337","summary":"The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1; MIM 601912) is required for many cellular processes. SUMO-specific proteases, such as SENP7, process SUMO precursors to generate a C-terminal diglycine motif required for the conjugation reaction. They also display isopeptidase activity for deconjugation of SUMO-conjugated substrates (Lima and Reverter, 2008 [PubMed 18799455]).[supplied by OMIM, Jun 2009]","start":101324205,"end":101513241,"strand":-1,"description":"SUMO1/sentrin specific peptidase 7 [Source:HGNC Symbol;Acc:HGNC:30402]"}, {"versioned_ensembl_gene_id":"ENSG00000267281.2","gene_symbol":"AC023509.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":53506688,"end":53625979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185313.6","gene_symbol":"SCN10A","gene_name":"sodium voltage-gated channel alpha subunit 10 [Source:HGNC Symbol;Acc:HGNC:10582]","synonyms":"Nav1.8,hPN3,SNS,PN3","biotype":"protein_coding","ncbi_id":"6336","summary":"The protein encoded by this gene is a tetrodotoxin-resistant voltage-gated sodium channel alpha subunit. The properties of the channel formed by the encoded transmembrane protein can be altered by interaction with different beta subunits. This protein may be involved in the onset of pain associated with peripheral neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":38696802,"end":38794010,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 10 [Source:HGNC Symbol;Acc:HGNC:10582]"}, {"versioned_ensembl_gene_id":"ENSG00000275488.1","gene_symbol":"AC023509.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53574632,"end":53576103,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170653.18","gene_symbol":"ATF7","gene_name":"activating transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:792]","synonyms":"ATFA","biotype":"protein_coding","ncbi_id":"11016","summary":null,"start":53507856,"end":53626410,"strand":-1,"description":"activating transcription factor 7 [Source:HGNC Symbol;Acc:HGNC:792]"}, {"versioned_ensembl_gene_id":"ENSG00000111678.10","gene_symbol":"C12orf57","gene_name":"chromosome 12 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:29521]","synonyms":"GRCC10,C10","biotype":"protein_coding","ncbi_id":"113246","summary":"This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]","start":6942978,"end":6946003,"strand":1,"description":"chromosome 12 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:29521]"}, {"versioned_ensembl_gene_id":"ENSG00000228850.1","gene_symbol":"CDY12P","gene_name":"chromodomain Y-linked 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:23856]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386734","summary":null,"start":22064698,"end":22065712,"strand":1,"description":"chromodomain Y-linked 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:23856]"}, {"versioned_ensembl_gene_id":"ENSG00000179428.2","gene_symbol":"AC073072.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22725395,"end":22727620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266613.1","gene_symbol":"AP001094.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8412129,"end":8414304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232029.1","gene_symbol":"ELOCP15","gene_name":"elongin C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38151]","synonyms":"TCEB1P15","biotype":"processed_pseudogene","ncbi_id":"100462877","summary":null,"start":22068820,"end":22069151,"strand":1,"description":"elongin C pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:38151]"}, {"versioned_ensembl_gene_id":"ENSG00000280215.1","gene_symbol":"AC021613.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21129990,"end":21130100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262481.5","gene_symbol":"TMEM256-PLSCR3","gene_name":"TMEM256-PLSCR3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49186]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529211","summary":"This locus represents naturally occurring read-through transcription between the neighboring chromosome 17 open reading frame 61 (C17orf61) and phospholipid scramblase 3 (PLSCR3) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Jan 2011]","start":7389734,"end":7404097,"strand":-1,"description":"TMEM256-PLSCR3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49186]"}, {"versioned_ensembl_gene_id":"ENSG00000229442.2","gene_symbol":"THEMIS3P","gene_name":"thymocyte selection associated family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:49196]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100420484","summary":null,"start":8486997,"end":8513849,"strand":1,"description":"thymocyte selection associated family member 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:49196]"}, {"versioned_ensembl_gene_id":"ENSG00000225212.4","gene_symbol":"AP001793.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8545635,"end":8546817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259947.1","gene_symbol":"LINC02124","gene_name":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371048","summary":null,"start":1889114,"end":1890434,"strand":1,"description":"long intergenic non-protein coding RNA 2124 [Source:HGNC Symbol;Acc:HGNC:52981]"}, {"versioned_ensembl_gene_id":"ENSG00000243766.7","gene_symbol":"HOTTIP","gene_name":"HOXA distal transcript antisense RNA [Source:HGNC Symbol;Acc:HGNC:37461]","synonyms":"RP1-170O19.3,NCRNA00213,HOXA13-AS1,HOXA-AS6","biotype":"antisense_RNA","ncbi_id":"100316868","summary":"This gene produces a long RNA in antisense to the HOXA gene cluster. This transcript may regulate expression of HOXA genes in cis. This gene is upregulated in tumors and is implicated in the promotion of cell proliferation. [provided by RefSeq, Dec 2017]","start":27198575,"end":27207259,"strand":1,"description":"HOXA distal transcript antisense RNA [Source:HGNC Symbol;Acc:HGNC:37461]"}, {"versioned_ensembl_gene_id":"ENSG00000254334.1","gene_symbol":"AC021355.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21298206,"end":21309449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068781.21","gene_symbol":"STON1-GTF2A1L","gene_name":"STON1-GTF2A1L readthrough [Source:HGNC Symbol;Acc:HGNC:30651]","synonyms":"SALF","biotype":"protein_coding","ncbi_id":"286749","summary":"STON1-GTF2A1L mRNAs are infrequent but naturally occurring read-through products of the neighboring STON1 and GTF2A1L genes. These transcripts encode fusion proteins composed of the vast majority of each of the individual elements, stonin 1 and general transcription factor IIA, 1-like. Alternative splicing results in multiple transcript variants. The significance of these read-through variants and the function of the resulting protein products have not yet been determined. [provided by RefSeq, Oct 2010]","start":48529925,"end":48776517,"strand":1,"description":"STON1-GTF2A1L readthrough [Source:HGNC Symbol;Acc:HGNC:30651]"}, {"versioned_ensembl_gene_id":"ENSG00000231013.1","gene_symbol":"AC013275.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119476448,"end":119487346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169807.10","gene_symbol":"PRY2","gene_name":"PTPN13-like, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:21504]","synonyms":"PTPN13LY2","biotype":"protein_coding","ncbi_id":"442862","summary":"This gene is located in the nonrecombining portion of the Y chromosome, and expressed specifically in testis. It encodes a protein which has a low degree of similarity to protein tyrosine phosphatase, non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":22071756,"end":22096007,"strand":-1,"description":"PTPN13-like, Y-linked 2 [Source:HGNC Symbol;Acc:HGNC:21504]"}, {"versioned_ensembl_gene_id":"ENSG00000261401.1","gene_symbol":"AC091304.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28332237,"end":28336609,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261561.1","gene_symbol":"AC091304.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28346490,"end":28346647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237850.7","gene_symbol":"AC091304.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28349051,"end":28358080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255839.1","gene_symbol":"AC117503.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":123707602,"end":123708386,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106031.7","gene_symbol":"HOXA13","gene_name":"homeobox A13 [Source:HGNC Symbol;Acc:HGNC:5102]","synonyms":"HOX1J,HOX1","biotype":"protein_coding","ncbi_id":"3209","summary":"In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. [provided by RefSeq, Jul 2008]","start":27193503,"end":27200106,"strand":-1,"description":"homeobox A13 [Source:HGNC Symbol;Acc:HGNC:5102]"}, {"versioned_ensembl_gene_id":"ENSG00000160233.7","gene_symbol":"LRRC3","gene_name":"leucine rich repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:14965]","synonyms":"C21orf102","biotype":"protein_coding","ncbi_id":"81543","summary":null,"start":44455486,"end":44462196,"strand":1,"description":"leucine rich repeat containing 3 [Source:HGNC Symbol;Acc:HGNC:14965]"}, {"versioned_ensembl_gene_id":"ENSG00000080293.9","gene_symbol":"SCTR","gene_name":"secretin receptor [Source:HGNC Symbol;Acc:HGNC:10608]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6344","summary":"The protein encoded by this gene is a G protein-coupled receptor and belongs to the glucagon-VIP-secretin receptor family. It binds secretin which is the most potent regulator of pancreatic bicarbonate, electrolyte and volume secretion. Secretin and its receptor are suggested to be involved in pancreatic cancer and autism. [provided by RefSeq, Jul 2008]","start":119439843,"end":119525301,"strand":-1,"description":"secretin receptor [Source:HGNC Symbol;Acc:HGNC:10608]"}, {"versioned_ensembl_gene_id":"ENSG00000213721.3","gene_symbol":"HMGN2P30","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39397]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131183","summary":null,"start":42113365,"end":42113620,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39397]"}, {"versioned_ensembl_gene_id":"ENSG00000235868.3","gene_symbol":"GAPDHP31","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643739","summary":null,"start":7566369,"end":7567382,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:37783]"}, {"versioned_ensembl_gene_id":"ENSG00000280346.1","gene_symbol":"FP236240.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6507017,"end":6507389,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163508.12","gene_symbol":"EOMES","gene_name":"eomesodermin [Source:HGNC Symbol;Acc:HGNC:3372]","synonyms":"TBR2","biotype":"protein_coding","ncbi_id":"8320","summary":"This gene belongs to the TBR1 (T-box brain protein 1) sub-family of T-box genes that share the common DNA-binding T-box domain. The encoded protein is a transcription factor which is crucial for embryonic development of mesoderm and the central nervous system in vertebrates. The protein may also be necessary for the differentiation of effector CD8+ T cells which are involved in defense against viral infections. A similar gene disrupted in mice is shown to be essential during trophoblast development and gastrulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":27715949,"end":27722711,"strand":-1,"description":"eomesodermin [Source:HGNC Symbol;Acc:HGNC:3372]"}, {"versioned_ensembl_gene_id":"ENSG00000279226.1","gene_symbol":"FP236240.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6520344,"end":6520670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278927.1","gene_symbol":"FP236240.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6550749,"end":6553955,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117118.9","gene_symbol":"SDHB","gene_name":"succinate dehydrogenase complex iron sulfur subunit B [Source:HGNC Symbol;Acc:HGNC:10681]","synonyms":"SDH,SDH1","biotype":"protein_coding","ncbi_id":"6390","summary":"Complex II of the respiratory chain, which is specifically involved in the oxidation of succinate, carries electrons from FADH to CoQ. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. The iron-sulfur subunit is highly conserved and contains three cysteine-rich clusters which may comprise the iron-sulfur centers of the enzyme. Sporadic and familial mutations in this gene result in paragangliomas and pheochromocytoma, and support a link between mitochondrial dysfunction and tumorigenesis. [provided by RefSeq, Jul 2008]","start":17018722,"end":17054170,"strand":-1,"description":"succinate dehydrogenase complex iron sulfur subunit B [Source:HGNC Symbol;Acc:HGNC:10681]"}, {"versioned_ensembl_gene_id":"ENSG00000240687.1","gene_symbol":"AC082651.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9638772,"end":9649439,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227212.3","gene_symbol":"PFN1P6","gene_name":"profilin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42988]","synonyms":"PFN1P7","biotype":"processed_pseudogene","ncbi_id":"645126","summary":null,"start":144442606,"end":144443004,"strand":1,"description":"profilin 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42988]"}, {"versioned_ensembl_gene_id":"ENSG00000244260.1","gene_symbol":"AC082651.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9674023,"end":9708413,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215296.10","gene_symbol":"TMCO5B","gene_name":"transmembrane and coiled-coil domains 5B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34243]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"100652857","summary":null,"start":33235552,"end":33247621,"strand":-1,"description":"transmembrane and coiled-coil domains 5B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34243]"}, {"versioned_ensembl_gene_id":"ENSG00000278216.3","gene_symbol":"UGT2A3","gene_name":"UDP glucuronosyltransferase family 2 member A3 [Source:HGNC Symbol;Acc:HGNC:28528]","synonyms":"FLJ21934","biotype":"protein_coding","ncbi_id":"79799","summary":null,"start":68810840,"end":68834168,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member A3 [Source:HGNC Symbol;Acc:HGNC:28528]"}, {"versioned_ensembl_gene_id":"ENSG00000122543.10","gene_symbol":"OCM","gene_name":"oncomodulin [Source:HGNC Symbol;Acc:HGNC:8105]","synonyms":"OCM1","biotype":"protein_coding","ncbi_id":"654231","summary":"Oncomodulin is a high-affinity calcium ion-binding protein. It belongs to the superfamily of calmodulin proteins, also known as the EF-hand proteins. Oncomodulin is an oncodevelopmental protein found in early embryonic cells in the placenta and also in tumors. [provided by RefSeq, Jul 2008]","start":5879827,"end":5886362,"strand":1,"description":"oncomodulin [Source:HGNC Symbol;Acc:HGNC:8105]"}, {"versioned_ensembl_gene_id":"ENSG00000273529.2","gene_symbol":"HES5","gene_name":"hes family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:19764]","synonyms":"bHLHb38","biotype":"protein_coding","ncbi_id":"388585","summary":"This gene encodes a member of a family of basic helix-loop-helix transcriptional repressors. The protein product of this gene, which is activated downstream of the Notch pathway, regulates cell differentiation in multiple tissues. Disruptions in the normal expression of this gene have been associated with developmental diseases and cancer. [provided by RefSeq, Dec 2008]","start":2528745,"end":2530245,"strand":-1,"description":"hes family bHLH transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:19764]"}, {"versioned_ensembl_gene_id":"ENSG00000099860.8","gene_symbol":"GADD45B","gene_name":"growth arrest and DNA damage inducible beta [Source:HGNC Symbol;Acc:HGNC:4096]","synonyms":"MYD118,GADD45BETA,DKFZP566B133","biotype":"protein_coding","ncbi_id":"4616","summary":"This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The genes in this group respond to environmental stresses by mediating activation of the p38/JNK pathway. This activation is mediated via their proteins binding and activating MTK1/MEKK4 kinase, which is an upstream activator of both p38 and JNK MAPKs. The function of these genes or their protein products is involved in the regulation of growth and apoptosis. These genes are regulated by different mechanisms, but they are often coordinately expressed and can function cooperatively in inhibiting cell growth. [provided by RefSeq, Jul 2008]","start":2476122,"end":2478259,"strand":1,"description":"growth arrest and DNA damage inducible beta [Source:HGNC Symbol;Acc:HGNC:4096]"}, {"versioned_ensembl_gene_id":"ENSG00000232978.2","gene_symbol":"AL161909.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19291337,"end":19292576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255993.1","gene_symbol":"PSMC1P9","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643668","summary":null,"start":18692762,"end":18694096,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39784]"}, {"versioned_ensembl_gene_id":"ENSG00000255648.1","gene_symbol":"AC087242.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18714795,"end":18737878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139151.14","gene_symbol":"PLCZ1","gene_name":"phospholipase C zeta 1 [Source:HGNC Symbol;Acc:HGNC:19218]","synonyms":"PLCzeta,NYD-SP27","biotype":"protein_coding","ncbi_id":"89869","summary":"The protein encoded by this gene is a member of the phosphoinositide-specific phospholipase C family. Members in this family, classified into six isotypes that are tissue- and organ-specific, hydrolyze phosphatidylinositol 4,5-bisphosphate just before the phosphate group to yield diacylglycerol and inositol 1,4,5-trisphosphate. This protein localizes to the acrosome in spermatozoa and elicits Ca(2+) oscillations and egg activation during fertilization that leads to early embryonic development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":18683169,"end":18738057,"strand":-1,"description":"phospholipase C zeta 1 [Source:HGNC Symbol;Acc:HGNC:19218]"}, {"versioned_ensembl_gene_id":"ENSG00000168546.10","gene_symbol":"GFRA2","gene_name":"GDNF family receptor alpha 2 [Source:HGNC Symbol;Acc:HGNC:4244]","synonyms":"TRNR2,RETL2,NTNRA,GDNFRB","biotype":"protein_coding","ncbi_id":"2675","summary":"Glial cell line-derived neurotrophic factor (GDNF) and neurturin (NTN) are two structurally related, potent neurotrophic factors that play key roles in the control of neuron survival and differentiation. The protein encoded by this gene is a member of the GDNF receptor family. It is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor for both GDNF and NTN, and mediates activation of the RET tyrosine kinase receptor. This encoded protein acts preferentially as a receptor for NTN compared to its other family member, GDNF family receptor alpha 1. This gene is a candidate gene for RET-associated diseases. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":21690403,"end":21812357,"strand":-1,"description":"GDNF family receptor alpha 2 [Source:HGNC Symbol;Acc:HGNC:4244]"}, {"versioned_ensembl_gene_id":"ENSG00000272842.1","gene_symbol":"AL391834.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19371386,"end":19371945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205544.3","gene_symbol":"TMEM256","gene_name":"transmembrane protein 256 [Source:HGNC Symbol;Acc:HGNC:28618]","synonyms":"MGC40107,C17orf61","biotype":"protein_coding","ncbi_id":"254863","summary":null,"start":7402975,"end":7404137,"strand":-1,"description":"transmembrane protein 256 [Source:HGNC Symbol;Acc:HGNC:28618]"}, {"versioned_ensembl_gene_id":"ENSG00000226578.1","gene_symbol":"AL132657.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37775371,"end":37784131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111247.14","gene_symbol":"RAD51AP1","gene_name":"RAD51 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16956]","synonyms":"PIR51","biotype":"protein_coding","ncbi_id":"10635","summary":null,"start":4538798,"end":4560048,"strand":1,"description":"RAD51 associated protein 1 [Source:HGNC Symbol;Acc:HGNC:16956]"}, {"versioned_ensembl_gene_id":"ENSG00000260137.1","gene_symbol":"AL132657.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37791580,"end":37791937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228828.1","gene_symbol":"TLK2P2","gene_name":"tousled like kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22227]","synonyms":"TLK2ps2","biotype":"processed_pseudogene","ncbi_id":"553121","summary":null,"start":37818606,"end":37820982,"strand":-1,"description":"tousled like kinase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22227]"}, {"versioned_ensembl_gene_id":"ENSG00000137145.20","gene_symbol":"DENND4C","gene_name":"DENN domain containing 4C [Source:HGNC Symbol;Acc:HGNC:26079]","synonyms":"RAB10GEF,FLJ20686,C9orf55B,C9orf55,bA513M16.3","biotype":"protein_coding","ncbi_id":"55667","summary":null,"start":19230435,"end":19373545,"strand":1,"description":"DENN domain containing 4C [Source:HGNC Symbol;Acc:HGNC:26079]"}, {"versioned_ensembl_gene_id":"ENSG00000236514.1","gene_symbol":"AL135791.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37857740,"end":37859110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225192.1","gene_symbol":"ZNF33BP1","gene_name":"zinc finger protein 33B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44975]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419868","summary":null,"start":37794276,"end":37796109,"strand":-1,"description":"zinc finger protein 33B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44975]"}, {"versioned_ensembl_gene_id":"ENSG00000236333.3","gene_symbol":"TRHDE-AS1","gene_name":"TRHDE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27471]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283392","summary":null,"start":72253508,"end":72274907,"strand":-1,"description":"TRHDE antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27471]"}, {"versioned_ensembl_gene_id":"ENSG00000214660.6","gene_symbol":"SLC29A4P2","gene_name":"solute carrier family 29 member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43782]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132308","summary":null,"start":63556598,"end":63562588,"strand":1,"description":"solute carrier family 29 member 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43782]"}, {"versioned_ensembl_gene_id":"ENSG00000278703.1","gene_symbol":"AC100847.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57588611,"end":57589091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230916.2","gene_symbol":"MTCO1P53","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:52118]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075285","summary":null,"start":126471705,"end":126472403,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:52118]"}, {"versioned_ensembl_gene_id":"ENSG00000237633.2","gene_symbol":"AC104623.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16523176,"end":16529387,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231501.1","gene_symbol":"MTND4LP1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31347]","synonyms":"MTND4L2","biotype":"processed_pseudogene","ncbi_id":"106478909","summary":null,"start":126472728,"end":126472884,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31347]"}, {"versioned_ensembl_gene_id":"ENSG00000186136.1","gene_symbol":"TAS2R42","gene_name":"taste 2 receptor member 42 [Source:HGNC Symbol;Acc:HGNC:18888]","synonyms":"TAS2R55,T2R55,T2R24,hT2R55","biotype":"protein_coding","ncbi_id":"353164","summary":null,"start":11185993,"end":11186937,"strand":-1,"description":"taste 2 receptor member 42 [Source:HGNC Symbol;Acc:HGNC:18888]"}, {"versioned_ensembl_gene_id":"ENSG00000266995.1","gene_symbol":"AP001542.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12040101,"end":12040300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260840.1","gene_symbol":"LINC01964","gene_name":"long intergenic non-protein coding RNA 1964 [Source:HGNC Symbol;Acc:HGNC:52789]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996478","summary":null,"start":85064108,"end":85067347,"strand":-1,"description":"long intergenic non-protein coding RNA 1964 [Source:HGNC Symbol;Acc:HGNC:52789]"}, {"versioned_ensembl_gene_id":"ENSG00000161180.10","gene_symbol":"CCDC116","gene_name":"coiled-coil domain containing 116 [Source:HGNC Symbol;Acc:HGNC:26688]","synonyms":"FLJ36046","biotype":"protein_coding","ncbi_id":"164592","summary":null,"start":21632716,"end":21637327,"strand":1,"description":"coiled-coil domain containing 116 [Source:HGNC Symbol;Acc:HGNC:26688]"}, {"versioned_ensembl_gene_id":"ENSG00000256657.1","gene_symbol":"AC244131.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11196075,"end":11196996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275119.1","gene_symbol":"AC244131.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11212219,"end":11251389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139287.12","gene_symbol":"TPH2","gene_name":"tryptophan hydroxylase 2 [Source:HGNC Symbol;Acc:HGNC:20692]","synonyms":"NTPH,FLJ37295","biotype":"protein_coding","ncbi_id":"121278","summary":"This gene encodes a member of the pterin-dependent aromatic acid hydroxylase family. The encoded protein catalyzes the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. Mutations in this gene may be associated with psychiatric diseases such as bipolar affective disorder and major depression. [provided by RefSeq, Feb 2016]","start":71938846,"end":72186618,"strand":1,"description":"tryptophan hydroxylase 2 [Source:HGNC Symbol;Acc:HGNC:20692]"}, {"versioned_ensembl_gene_id":"ENSG00000241923.2","gene_symbol":"RPL14P3","gene_name":"ribosomal protein L14 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36638]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730747","summary":null,"start":140366240,"end":140366861,"strand":-1,"description":"ribosomal protein L14 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:36638]"}, {"versioned_ensembl_gene_id":"ENSG00000223566.1","gene_symbol":"TNRC18P2","gene_name":"trinucleotide repeat containing 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34014]","synonyms":"TNRC18B","biotype":"unprocessed_pseudogene","ncbi_id":"27320","summary":null,"start":63567743,"end":63585075,"strand":-1,"description":"trinucleotide repeat containing 18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:34014]"}, {"versioned_ensembl_gene_id":"ENSG00000235463.1","gene_symbol":"AC078974.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85068809,"end":85069031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153130.17","gene_symbol":"SCOC","gene_name":"short coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:20335]","synonyms":"UNC-69,SCOCO,HRIHFB2072","biotype":"protein_coding","ncbi_id":"60592","summary":"This gene encodes a short coiled-coiled domain-containing protein that localizes to the Golgi apparatus. The encoded protein interacts with ADP-ribosylation factor-like proteins. Pseudogenes of this gene are found on chromosomes 1 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":140257286,"end":140385726,"strand":1,"description":"short coiled-coil protein [Source:HGNC Symbol;Acc:HGNC:20335]"}, {"versioned_ensembl_gene_id":"ENSG00000274901.1","gene_symbol":"Z69908.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126502898,"end":126503144,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198889.4","gene_symbol":"DCAF12L1","gene_name":"DDB1 and CUL4 associated factor 12 like 1 [Source:HGNC Symbol;Acc:HGNC:29395]","synonyms":"WDR40B,KIAA1892L","biotype":"protein_coding","ncbi_id":"139170","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]","start":126549383,"end":126552851,"strand":-1,"description":"DDB1 and CUL4 associated factor 12 like 1 [Source:HGNC Symbol;Acc:HGNC:29395]"}, {"versioned_ensembl_gene_id":"ENSG00000275576.1","gene_symbol":"AL049539.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":32116171,"end":32116629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187838.16","gene_symbol":"PLSCR3","gene_name":"phospholipid scramblase 3 [Source:HGNC Symbol;Acc:HGNC:16495]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57048","summary":null,"start":7389727,"end":7394843,"strand":-1,"description":"phospholipid scramblase 3 [Source:HGNC Symbol;Acc:HGNC:16495]"}, {"versioned_ensembl_gene_id":"ENSG00000225787.1","gene_symbol":"LSM3P3","gene_name":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44348]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647302","summary":null,"start":85102389,"end":85102694,"strand":-1,"description":"LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44348]"}, {"versioned_ensembl_gene_id":"ENSG00000255071.3","gene_symbol":"SAA2-SAA4","gene_name":"SAA2-SAA4 readthrough [Source:HGNC Symbol;Acc:HGNC:39550]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100528017","summary":"This locus represents naturally occurring read-through transcription between the neighboring serum amyloid A2 and serum amyloid A4 genes on chromosome 11. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Dec 2010]","start":18231423,"end":18248635,"strand":-1,"description":"SAA2-SAA4 readthrough [Source:HGNC Symbol;Acc:HGNC:39550]"}, {"versioned_ensembl_gene_id":"ENSG00000273342.1","gene_symbol":"AP000553.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21640844,"end":21641284,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277177.4","gene_symbol":"LILRA6","gene_name":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]","synonyms":"CD85b,LILRB6,ILT8","biotype":"protein_coding","ncbi_id":"79168","summary":null,"start":54216894,"end":54243483,"strand":-1,"description":"leukocyte immunoglobulin like receptor A6 [Source:HGNC Symbol;Acc:HGNC:15495]"}, {"versioned_ensembl_gene_id":"ENSG00000181126.13","gene_symbol":"HLA-V","gene_name":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]","synonyms":"dJ377H14.4,HLA-75","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352962","summary":null,"start":29790954,"end":29797811,"strand":1,"description":"major histocompatibility complex, class I, V (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23482]"}, {"versioned_ensembl_gene_id":"ENSG00000234135.2","gene_symbol":"RPL23AP83","gene_name":"ribosomal protein L23a pseudogene 83 [Source:HGNC Symbol;Acc:HGNC:35846]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131846","summary":null,"start":56242937,"end":56243409,"strand":-1,"description":"ribosomal protein L23a pseudogene 83 [Source:HGNC Symbol;Acc:HGNC:35846]"}, {"versioned_ensembl_gene_id":"ENSG00000179813.6","gene_symbol":"FAM216B","gene_name":"family with sequence similarity 216 member B [Source:HGNC Symbol;Acc:HGNC:26883]","synonyms":"FLJ40919,C13orf30","biotype":"protein_coding","ncbi_id":"144809","summary":null,"start":42781550,"end":42791549,"strand":1,"description":"family with sequence similarity 216 member B [Source:HGNC Symbol;Acc:HGNC:26883]"}, {"versioned_ensembl_gene_id":"ENSG00000227933.1","gene_symbol":"AL357874.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35646270,"end":35647099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128228.4","gene_symbol":"SDF2L1","gene_name":"stromal cell derived factor 2 like 1 [Source:HGNC Symbol;Acc:HGNC:10676]","synonyms":"OTTHUMT00000075032,AP000553.C22.4","biotype":"protein_coding","ncbi_id":"23753","summary":null,"start":21642261,"end":21644298,"strand":1,"description":"stromal cell derived factor 2 like 1 [Source:HGNC Symbol;Acc:HGNC:10676]"}, {"versioned_ensembl_gene_id":"ENSG00000102349.17","gene_symbol":"KLF8","gene_name":"Kruppel like factor 8 [Source:HGNC Symbol;Acc:HGNC:6351]","synonyms":"ZNF741,DXS741,BKLF3","biotype":"protein_coding","ncbi_id":"11279","summary":"This gene encodes a protein which is a member of the Sp/KLF family of transcription factors. Members of this family contain a C-terminal DNA-binding domain with three Kruppel-like zinc fingers. The encoded protein is thought to play an important role in the regulation of epithelial to mesenchymal transition, a process which occurs normally during development but also during metastasis. A pseudogene has been identified on chromosome 16. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]","start":56232421,"end":56287889,"strand":1,"description":"Kruppel like factor 8 [Source:HGNC Symbol;Acc:HGNC:6351]"}, {"versioned_ensembl_gene_id":"ENSG00000107140.15","gene_symbol":"TESK1","gene_name":"testis-specific kinase 1 [Source:HGNC Symbol;Acc:HGNC:11731]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7016","summary":"This gene product is a serine/threonine protein kinase that contains an N-terminal protein kinase domain and a C-terminal proline-rich domain. Its protein kinase domain is most closely related to those of the LIM motif-containing protein kinases (LIMKs). The encoded protein can phosphorylate myelin basic protein and histone in vitro. The testicular germ cell-specific expression and developmental pattern of expression of the mouse gene suggests that this gene plays an important role at and after the meiotic phase of spermatogenesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":35605305,"end":35610041,"strand":1,"description":"testis-specific kinase 1 [Source:HGNC Symbol;Acc:HGNC:11731]"}, {"versioned_ensembl_gene_id":"ENSG00000240960.1","gene_symbol":"AC082651.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9746704,"end":9746869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250516.1","gene_symbol":"AC021678.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28225929,"end":28227562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259474.1","gene_symbol":"AC027228.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78480057,"end":78481820,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236867.1","gene_symbol":"Z98885.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49817248,"end":49817712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261814.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"C6orf101,HLA-90,dJ377H14.3","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29797637,"end":29799645,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000226955.1","gene_symbol":"AC104306.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32592972,"end":32593312,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000148965.9","gene_symbol":"SAA4","gene_name":"serum amyloid A4, constitutive [Source:HGNC Symbol;Acc:HGNC:10516]","synonyms":"CSAA,C-SAA","biotype":"protein_coding","ncbi_id":"6291","summary":null,"start":18231349,"end":18236893,"strand":-1,"description":"serum amyloid A4, constitutive [Source:HGNC Symbol;Acc:HGNC:10516]"}, {"versioned_ensembl_gene_id":"ENSG00000176998.4","gene_symbol":"HCG4","gene_name":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]","synonyms":"HCGIV-10,HCG4P10,HCGIV.9","biotype":"unprocessed_pseudogene","ncbi_id":"54435","summary":null,"start":29791753,"end":29792750,"strand":-1,"description":"HLA complex group 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21241]"}, {"versioned_ensembl_gene_id":"ENSG00000237676.1","gene_symbol":"RPL30P4","gene_name":"ribosomal protein L30 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35871]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131230","summary":null,"start":32635222,"end":32635554,"strand":-1,"description":"ribosomal protein L30 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:35871]"}, {"versioned_ensembl_gene_id":"ENSG00000238141.2","gene_symbol":"BRWD1-AS1","gene_name":"BRWD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40614]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874093","summary":null,"start":39315707,"end":39323218,"strand":1,"description":"BRWD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40614]"}, {"versioned_ensembl_gene_id":"ENSG00000253308.2","gene_symbol":"AC004080.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27239243,"end":27241228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206418.3","gene_symbol":"RAB12","gene_name":"RAB12, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:31332]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201475","summary":null,"start":8609445,"end":8639381,"strand":1,"description":"RAB12, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:31332]"}, {"versioned_ensembl_gene_id":"ENSG00000281189.1","gene_symbol":"GHET1","gene_name":"gastric carcinoma proliferation enhancing transcript 1 [Source:HGNC Symbol;Acc:HGNC:49425]","synonyms":"lncRNA-GHET1","biotype":"lincRNA","ncbi_id":"102723099","summary":"This gene encodes an unspliced long non-coding RNA that has been suggested to promote the proliferation of gastric carcinoma cells and bladder cancer cells. [provided by RefSeq, Dec 2014]","start":148987527,"end":148989432,"strand":1,"description":"gastric carcinoma proliferation enhancing transcript 1 [Source:HGNC Symbol;Acc:HGNC:49425]"}, {"versioned_ensembl_gene_id":"ENSG00000226414.1","gene_symbol":"MTCYBP38","gene_name":"mitochondrially encoded cytochrome b pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52306]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729117","summary":null,"start":126729104,"end":126730226,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:52306]"}, {"versioned_ensembl_gene_id":"ENSG00000230785.2","gene_symbol":"AC006326.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117262918,"end":117264888,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232608.1","gene_symbol":"TIMM9P2","gene_name":"TIMM9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862727","summary":null,"start":39216624,"end":39217506,"strand":1,"description":"TIMM9 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39929]"}, {"versioned_ensembl_gene_id":"ENSG00000259446.5","gene_symbol":"AC055874.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33303657,"end":33310659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272991.1","gene_symbol":"AF129408.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39184469,"end":39184899,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254642.1","gene_symbol":"COX6CP5","gene_name":"cytochrome c oxidase subunit 6C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42791]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100862855","summary":null,"start":7977481,"end":7977708,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42791]"}, {"versioned_ensembl_gene_id":"ENSG00000170262.12","gene_symbol":"MRAP","gene_name":"melanocortin 2 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:1304]","synonyms":"FALP,C21orf61,B27","biotype":"protein_coding","ncbi_id":"56246","summary":"This gene encodes a melanocortin receptor-interacting protein. The encoded protein regulates trafficking and function of the melanocortin 2 receptor in the adrenal gland. The encoded protein can also modulate signaling of other melanocortin receptors. Mutations in this gene have been associated with familial glucocorticoid deficiency type 2. Alternatively spliced transcript variants have been described. [provided by RefSeq, Dec 2009]","start":32291813,"end":32314784,"strand":1,"description":"melanocortin 2 receptor accessory protein [Source:HGNC Symbol;Acc:HGNC:1304]"}, {"versioned_ensembl_gene_id":"ENSG00000271216.1","gene_symbol":"LINC01050","gene_name":"long intergenic non-protein coding RNA 1050 [Source:HGNC Symbol;Acc:HGNC:49044]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103689845","summary":null,"start":42810366,"end":42812562,"strand":-1,"description":"long intergenic non-protein coding RNA 1050 [Source:HGNC Symbol;Acc:HGNC:49044]"}, {"versioned_ensembl_gene_id":"ENSG00000229623.1","gene_symbol":"METTL21AP1","gene_name":"methyltransferase like 21A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41921]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421629","summary":null,"start":39235386,"end":39236020,"strand":-1,"description":"methyltransferase like 21A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:41921]"}, {"versioned_ensembl_gene_id":"ENSG00000175390.13","gene_symbol":"EIF3F","gene_name":"eukaryotic translation initiation factor 3 subunit F [Source:HGNC Symbol;Acc:HGNC:3275]","synonyms":"eIF3-p47,eIF3-epsilon,EIF3S5,eIF3f","biotype":"protein_coding","ncbi_id":"8665","summary":null,"start":7970251,"end":8001862,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit F [Source:HGNC Symbol;Acc:HGNC:3275]"}, {"versioned_ensembl_gene_id":"ENSG00000261548.1","gene_symbol":"HLA-P","gene_name":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]","synonyms":"C6orf101,HLA-90,dJ377H14.3","biotype":"unprocessed_pseudogene","ncbi_id":"352963","summary":null,"start":29800415,"end":29802425,"strand":1,"description":"major histocompatibility complex, class I, P (pseudogene) [Source:HGNC Symbol;Acc:HGNC:21196]"}, {"versioned_ensembl_gene_id":"ENSG00000227646.7","gene_symbol":"STEAP2-AS1","gene_name":"STEAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40820]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100874100","summary":null,"start":89882353,"end":90211635,"strand":-1,"description":"STEAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40820]"}, {"versioned_ensembl_gene_id":"ENSG00000230605.1","gene_symbol":"MTCYBP6","gene_name":"mitochondrially encoded cytochrome b pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51974]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075259","summary":null,"start":117264393,"end":117264530,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:51974]"}, {"versioned_ensembl_gene_id":"ENSG00000226558.1","gene_symbol":"AL590383.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43364220,"end":43364294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224042.2","gene_symbol":"MTND4P6","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42193]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873192","summary":null,"start":117263917,"end":117264388,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42193]"}, {"versioned_ensembl_gene_id":"ENSG00000220614.1","gene_symbol":"AL583834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43328134,"end":43328476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226915.1","gene_symbol":"AC068137.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130293822,"end":130294405,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179157.4","gene_symbol":"RPS2P28","gene_name":"ribosomal protein S2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35780]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132673","summary":null,"start":43363479,"end":43364219,"strand":1,"description":"ribosomal protein S2 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35780]"}, {"versioned_ensembl_gene_id":"ENSG00000229546.1","gene_symbol":"LINC00428","gene_name":"long intergenic non-protein coding RNA 428 [Source:HGNC Symbol;Acc:HGNC:42763]","synonyms":null,"biotype":"lincRNA","ncbi_id":"104355147","summary":null,"start":42842414,"end":42842887,"strand":-1,"description":"long intergenic non-protein coding RNA 428 [Source:HGNC Symbol;Acc:HGNC:42763]"}, {"versioned_ensembl_gene_id":"ENSG00000253457.2","gene_symbol":"SMIM18","gene_name":"small integral membrane protein 18 [Source:HGNC Symbol;Acc:HGNC:42973]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100507341","summary":null,"start":30638600,"end":30646064,"strand":1,"description":"small integral membrane protein 18 [Source:HGNC Symbol;Acc:HGNC:42973]"}, {"versioned_ensembl_gene_id":"ENSG00000185658.13","gene_symbol":"BRWD1","gene_name":"bromodomain and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:12760]","synonyms":"WDR9,N143,FLJ11315,DCAF19,C21orf107","biotype":"protein_coding","ncbi_id":"54014","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.[provided by RefSeq, Jun 2011]","start":39184176,"end":39321559,"strand":-1,"description":"bromodomain and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:HGNC:12760]"}, {"versioned_ensembl_gene_id":"ENSG00000257723.1","gene_symbol":"CHCHD3P2","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44698]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422354","summary":null,"start":72610678,"end":72611316,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44698]"}, {"versioned_ensembl_gene_id":"ENSG00000243491.1","gene_symbol":"AC082651.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9757496,"end":9770341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230538.1","gene_symbol":"Z82209.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127390342,"end":127392526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164647.8","gene_symbol":"STEAP1","gene_name":"STEAP family member 1 [Source:HGNC Symbol;Acc:HGNC:11378]","synonyms":"STEAP,PRSS24","biotype":"protein_coding","ncbi_id":"26872","summary":"This gene is predominantly expressed in prostate tissue, and is found to be upregulated in multiple cancer cell lines. The gene product is predicted to be a six-transmembrane protein, and was shown to be a cell surface antigen significantly expressed at cell-cell junctions. [provided by RefSeq, Jul 2008]","start":90154375,"end":90164829,"strand":1,"description":"STEAP family member 1 [Source:HGNC Symbol;Acc:HGNC:11378]"}, {"versioned_ensembl_gene_id":"ENSG00000205730.6","gene_symbol":"ITPRIPL2","gene_name":"inositol 1,4,5-trisphosphate receptor interacting protein like 2 [Source:HGNC Symbol;Acc:HGNC:27257]","synonyms":"MGC126800,MGC126798,LOC162073,FLJ22994","biotype":"protein_coding","ncbi_id":"162073","summary":null,"start":19113932,"end":19121629,"strand":1,"description":"inositol 1,4,5-trisphosphate receptor interacting protein like 2 [Source:HGNC Symbol;Acc:HGNC:27257]"}, {"versioned_ensembl_gene_id":"ENSG00000271435.1","gene_symbol":"AC068137.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":130313934,"end":130314411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240731.1","gene_symbol":"AL139287.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":1317581,"end":1318689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219222.1","gene_symbol":"RPL12P47","gene_name":"ribosomal protein L12 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:51939]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075115","summary":null,"start":43310231,"end":43310357,"strand":1,"description":"ribosomal protein L12 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:51939]"}, {"versioned_ensembl_gene_id":"ENSG00000227030.2","gene_symbol":"CR759769.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29800417,"end":29801213,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250264.1","gene_symbol":"AL669918.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32813767,"end":32838822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224352.1","gene_symbol":"AC132479.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":130330142,"end":130330285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226589.9","gene_symbol":"VARS","gene_name":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]","synonyms":"VARS2","biotype":"protein_coding","ncbi_id":"7407","summary":"Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. The protein encoded by this gene belongs to class-I aminoacyl-tRNA synthetase family and is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":31764879,"end":31783312,"strand":-1,"description":"valyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:12651]"}, {"versioned_ensembl_gene_id":"ENSG00000205221.12","gene_symbol":"VIT","gene_name":"vitrin [Source:HGNC Symbol;Acc:HGNC:12697]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5212","summary":"This gene encodes an extracellular matrix (ECM) protein. The protein may be associated with cell adhesion and migration. High levels of expression of the protein in specific parts of the brain suggest its likely role in neural development. [provided by RefSeq, Jun 2016]","start":36696690,"end":36814792,"strand":1,"description":"vitrin [Source:HGNC Symbol;Acc:HGNC:12697]"}, {"versioned_ensembl_gene_id":"ENSG00000171467.15","gene_symbol":"ZNF318","gene_name":"zinc finger protein 318 [Source:HGNC Symbol;Acc:HGNC:13578]","synonyms":"ZFP318,HRIHFB2436","biotype":"protein_coding","ncbi_id":"24149","summary":null,"start":43307134,"end":43369478,"strand":-1,"description":"zinc finger protein 318 [Source:HGNC Symbol;Acc:HGNC:13578]"}, {"versioned_ensembl_gene_id":"ENSG00000183631.4","gene_symbol":"PRR32","gene_name":"proline rich 32 [Source:HGNC Symbol;Acc:HGNC:34498]","synonyms":"CXorf64","biotype":"protein_coding","ncbi_id":"100130613","summary":null,"start":126819764,"end":126821786,"strand":1,"description":"proline rich 32 [Source:HGNC Symbol;Acc:HGNC:34498]"}, {"versioned_ensembl_gene_id":"ENSG00000253405.1","gene_symbol":"EVX1-AS","gene_name":"EVX1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40223]","synonyms":"EVX1-AS1","biotype":"antisense_RNA","ncbi_id":"101410536","summary":null,"start":27241429,"end":27247229,"strand":-1,"description":"EVX1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:40223]"}, {"versioned_ensembl_gene_id":"ENSG00000277880.1","gene_symbol":"AC244472.5","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142601628,"end":142602360,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231785.1","gene_symbol":"MICC","gene_name":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]","synonyms":"PERB11.3","biotype":"unprocessed_pseudogene","ncbi_id":"100129192","summary":null,"start":30404626,"end":30409231,"strand":1,"description":"MHC class I polypeptide-related sequence C (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7092]"}, {"versioned_ensembl_gene_id":"ENSG00000241106.6","gene_symbol":"HLA-DOB","gene_name":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3112","summary":"HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32812763,"end":32817048,"strand":-1,"description":"major histocompatibility complex, class II, DO beta [Source:HGNC Symbol;Acc:HGNC:4937]"}, {"versioned_ensembl_gene_id":"ENSG00000213880.3","gene_symbol":"AL645939.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29803195,"end":29803991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197265.8","gene_symbol":"GTF2E2","gene_name":"general transcription factor IIE subunit 2 [Source:HGNC Symbol;Acc:HGNC:4651]","synonyms":"TFIIE-B,TF2E2,FE","biotype":"protein_coding","ncbi_id":"2961","summary":"The general transcription factor IIE (TFIIE) is part of the RNA polymerase II transcription initiation complex, recruiting TFIIH and being essential for promoter clearance by RNA polymerase II. TFIIE is a heterodimer (and sometimes heterotetramer) of alpha and beta subunits. The protein encoded by this gene represents the beta subunit of TFIIE. [provided by RefSeq, Jan 2017]","start":30578318,"end":30658251,"strand":-1,"description":"general transcription factor IIE subunit 2 [Source:HGNC Symbol;Acc:HGNC:4651]"}, {"versioned_ensembl_gene_id":"ENSG00000276557.1","gene_symbol":"AC244472.3","gene_name":null,"synonyms":null,"biotype":"TR_V_gene","ncbi_id":null,"summary":null,"start":142615716,"end":142616415,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106038.12","gene_symbol":"EVX1","gene_name":"even-skipped homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3506]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2128","summary":"This gene encodes a member of the even-skipped homeobox family characterized by the presence of a homeodomain closely related to the Drosophila even-skipped (eve) segmentation gene of the pair-rule class. The encoded protein may play an important role as a transcriptional repressor during embryogenesis. [provided by RefSeq, Jul 2008]","start":27242700,"end":27250493,"strand":1,"description":"even-skipped homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3506]"}, {"versioned_ensembl_gene_id":"ENSG00000127054.20","gene_symbol":"INTS11","gene_name":"integrator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:26052]","synonyms":"INT11,RC-68,FLJ20542,CPSF73L,CPSF3L","biotype":"protein_coding","ncbi_id":"54973","summary":"The Integrator complex contains at least 12 subunits and associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates the 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690). INTS11, or CPSF3L, is the catalytic subunit of the Integrator complex (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]","start":1311585,"end":1324691,"strand":-1,"description":"integrator complex subunit 11 [Source:HGNC Symbol;Acc:HGNC:26052]"}, {"versioned_ensembl_gene_id":"ENSG00000258115.1","gene_symbol":"AC090109.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":72046149,"end":72057377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266708.1","gene_symbol":"AP001793.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8635179,"end":8636347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257287.1","gene_symbol":"AC016256.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":72431722,"end":72432075,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229647.1","gene_symbol":"MYOSLID","gene_name":"myocardin-induced smooth muscle lncRNA, inducer of differentiation [Source:HGNC Symbol;Acc:HGNC:51821]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373853","summary":null,"start":207239650,"end":207245887,"strand":1,"description":"myocardin-induced smooth muscle lncRNA, inducer of differentiation [Source:HGNC Symbol;Acc:HGNC:51821]"}, {"versioned_ensembl_gene_id":"ENSG00000225763.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29809789,"end":29809920,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000211746.3","gene_symbol":"TRBV19","gene_name":"T-cell receptor beta variable 19 [Source:HGNC Symbol;Acc:HGNC:12194]","synonyms":"TCRBV19S1,TCRBV17S1A1T","biotype":"TR_V_gene","ncbi_id":"28568","summary":null,"start":142618849,"end":142619532,"strand":1,"description":"T-cell receptor beta variable 19 [Source:HGNC Symbol;Acc:HGNC:12194]"}, {"versioned_ensembl_gene_id":"ENSG00000255328.1","gene_symbol":"AC136475.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":327171,"end":330122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279566.1","gene_symbol":"ZNF43","gene_name":"zinc finger protein 43 [Source:HGNC Symbol;Acc:HGNC:13109]","synonyms":"ZNF39L1,KOX27,HTF6","biotype":"protein_coding","ncbi_id":"7594","summary":"This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008]","start":21814429,"end":21818511,"strand":-1,"description":"zinc finger protein 43 [Source:HGNC Symbol;Acc:HGNC:13109]"}, {"versioned_ensembl_gene_id":"ENSG00000213352.3","gene_symbol":"GAPDHP44","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:37801]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240709","summary":null,"start":62755227,"end":62756233,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:37801]"}, {"versioned_ensembl_gene_id":"ENSG00000155660.10","gene_symbol":"PDIA4","gene_name":"protein disulfide isomerase family A member 4 [Source:HGNC Symbol;Acc:HGNC:30167]","synonyms":"ERP72,ERP70","biotype":"protein_coding","ncbi_id":"9601","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal ER-signal sequence, three catalytically active thioredoxin (TRX) domains, two TRX-like domains and a C-terminal ER-retention sequence. This protein, when bound to cyclophilin B, enhances the rate of immunoglobulin G intermolecular disulfide bonding and antibody assembly. [provided by RefSeq, Dec 2016]","start":149003062,"end":149028641,"strand":-1,"description":"protein disulfide isomerase family A member 4 [Source:HGNC Symbol;Acc:HGNC:30167]"}, {"versioned_ensembl_gene_id":"ENSG00000111110.11","gene_symbol":"PPM1H","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1H [Source:HGNC Symbol;Acc:HGNC:18583]","synonyms":"NERPP-2C,KIAA1157,FLJ13253,ARHCL1","biotype":"protein_coding","ncbi_id":"57460","summary":null,"start":62643982,"end":62935037,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1H [Source:HGNC Symbol;Acc:HGNC:18583]"}, {"versioned_ensembl_gene_id":"ENSG00000257366.1","gene_symbol":"AC138969.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16308542,"end":16310000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144401.14","gene_symbol":"METTL21A","gene_name":"methyltransferase like 21A [Source:HGNC Symbol;Acc:HGNC:30476]","synonyms":"FAM119A,LOC151194,HSPA-KMT,HCA557b","biotype":"protein_coding","ncbi_id":"151194","summary":null,"start":207580631,"end":207625928,"strand":-1,"description":"methyltransferase like 21A [Source:HGNC Symbol;Acc:HGNC:30476]"}, {"versioned_ensembl_gene_id":"ENSG00000131548.7","gene_symbol":"TTTY6B","gene_name":"testis-specific transcript, Y-linked 6B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31887]","synonyms":"LINC00128","biotype":"antisense_RNA","ncbi_id":"441543","summary":"There are two copies of this locus in the P3 palindrome on chromosome Y. This record represents the more centromeric copy. [provided by RefSeq, Jul 2008]","start":22144966,"end":22146831,"strand":1,"description":"testis-specific transcript, Y-linked 6B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31887]"}, {"versioned_ensembl_gene_id":"ENSG00000232623.1","gene_symbol":"AP000266.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32306464,"end":32308737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236951.5","gene_symbol":"AC007359.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22100814,"end":22147484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277518.3","gene_symbol":"MUC6","gene_name":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"4588","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. [provided by RefSeq, Dec 2016]","start":1012821,"end":1043528,"strand":-1,"description":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]"}, {"versioned_ensembl_gene_id":"ENSG00000226861.1","gene_symbol":"AL390835.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8298897,"end":8301667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170989.8","gene_symbol":"S1PR1","gene_name":"sphingosine-1-phosphate receptor 1 [Source:HGNC Symbol;Acc:HGNC:3165]","synonyms":"EDG1,edg-1,D1S3362,CD363","biotype":"protein_coding","ncbi_id":"1901","summary":"The protein encoded by this gene is structurally similar to G protein-coupled receptors and is highly expressed in endothelial cells. It binds the ligand sphingosine-1-phosphate with high affinity and high specificity, and suggested to be involved in the processes that regulate the differentiation of endothelial cells. Activation of this receptor induces cell-cell adhesion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":101236888,"end":101241518,"strand":1,"description":"sphingosine-1-phosphate receptor 1 [Source:HGNC Symbol;Acc:HGNC:3165]"}, {"versioned_ensembl_gene_id":"ENSG00000125818.17","gene_symbol":"PSMF1","gene_name":"proteasome inhibitor subunit 1 [Source:HGNC Symbol;Acc:HGNC:9571]","synonyms":"PI31","biotype":"protein_coding","ncbi_id":"9491","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a protein that inhibits the activation of the proteasome by the 11S and 19S regulators. Alternative transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]","start":1113263,"end":1189415,"strand":1,"description":"proteasome inhibitor subunit 1 [Source:HGNC Symbol;Acc:HGNC:9571]"}, {"versioned_ensembl_gene_id":"ENSG00000228995.1","gene_symbol":"MTND1P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42099]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873221","summary":null,"start":57357426,"end":57358369,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42099]"}, {"versioned_ensembl_gene_id":"ENSG00000142207.6","gene_symbol":"URB1","gene_name":"URB1 ribosome biogenesis 1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:17344]","synonyms":"NPA1,KIAA0539,C21orf108","biotype":"protein_coding","ncbi_id":"9875","summary":null,"start":32311018,"end":32393026,"strand":-1,"description":"URB1 ribosome biogenesis 1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:HGNC:17344]"}, {"versioned_ensembl_gene_id":"ENSG00000256222.2","gene_symbol":"MTRNR2L3","gene_name":"MT-RNR2-like 3 [Source:HGNC Symbol;Acc:HGNC:37157]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100462983","summary":null,"start":57358442,"end":57359980,"strand":-1,"description":"MT-RNR2-like 3 [Source:HGNC Symbol;Acc:HGNC:37157]"}, {"versioned_ensembl_gene_id":"ENSG00000112812.15","gene_symbol":"PRSS16","gene_name":"protease, serine 16 [Source:HGNC Symbol;Acc:HGNC:9480]","synonyms":"TSSP","biotype":"protein_coding","ncbi_id":"10279","summary":"This gene encodes a serine protease expressed exclusively in the thymus. It is thought to play a role in the alternative antigen presenting pathway used by cortical thymic epithelial cells during the positive selection of T cells. The gene is found in the large histone gene cluster on chromosome 6, near the major histocompatibility complex (MHC) class I region. A second transcript variant has been described, but its full length nature has not been determined. [provided by RefSeq, Jul 2008]","start":27247701,"end":27256624,"strand":1,"description":"protease, serine 16 [Source:HGNC Symbol;Acc:HGNC:9480]"}, {"versioned_ensembl_gene_id":"ENSG00000281734.1","gene_symbol":"AL139246.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2546465,"end":2547460,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101146.12","gene_symbol":"RAE1","gene_name":"ribonucleic acid export 1 [Source:HGNC Symbol;Acc:HGNC:9828]","synonyms":"Mnrp41","biotype":"protein_coding","ncbi_id":"8480","summary":"Mutations in the Schizosaccharomyces pombe Rae1 and Saccharomyces cerevisiae Gle2 genes have been shown to result in accumulation of poly(A)-containing mRNA in the nucleus, suggesting that the encoded proteins are involved in RNA export. The protein encoded by this gene is a homolog of yeast Rae1. It contains four WD40 motifs, and has been shown to localize to distinct foci in the nucleoplasm, to the nuclear rim, and to meshwork-like structures throughout the cytoplasm. This gene is thought to be involved in nucleocytoplasmic transport, and in directly or indirectly attaching cytoplasmic mRNPs to the cytoskeleton. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":57351010,"end":57379211,"strand":1,"description":"ribonucleic acid export 1 [Source:HGNC Symbol;Acc:HGNC:9828]"}, {"versioned_ensembl_gene_id":"ENSG00000197870.12","gene_symbol":"PRB3","gene_name":"proline rich protein BstNI subfamily 3 [Source:HGNC Symbol;Acc:HGNC:9339]","synonyms":"PRG","biotype":"protein_coding","ncbi_id":"5544","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Long\" allele. The protein isoforms encoded by this gene are recognized as the \"first line of oral defense\" against the detrimental effects of polyphenols in the diet and pathogen infections. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Nov 2015]","start":11265924,"end":11269805,"strand":-1,"description":"proline rich protein BstNI subfamily 3 [Source:HGNC Symbol;Acc:HGNC:9339]"}, {"versioned_ensembl_gene_id":"ENSG00000270030.1","gene_symbol":"AC136475.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":325703,"end":326294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142089.15","gene_symbol":"IFITM3","gene_name":"interferon induced transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:5414]","synonyms":"1-8U","biotype":"protein_coding","ncbi_id":"10410","summary":"The protein encoded by this gene is an interferon-induced membrane protein that helps confer immunity to influenza A H1N1 virus, West Nile virus, and dengue virus. Two transcript variants, only one of them protein-coding, have been found for this gene. Another variant encoding an N-terminally truncated isoform has been reported, but the full-length nature of this variant has not been determined. [provided by RefSeq, May 2012]","start":319669,"end":327537,"strand":-1,"description":"interferon induced transmembrane protein 3 [Source:HGNC Symbol;Acc:HGNC:5414]"}, {"versioned_ensembl_gene_id":"ENSG00000002586.18","gene_symbol":"CD99","gene_name":"CD99 molecule (Xg blood group) [Source:HGNC Symbol;Acc:HGNC:7082]","synonyms":"MIC2","biotype":"protein_coding","ncbi_id":"4267","summary":"The protein encoded by this gene is a cell surface glycoprotein involved in leukocyte migration, T-cell adhesion, ganglioside GM1 and transmembrane protein transport, and T-cell death by a caspase-independent pathway. In addition, the encoded protein may have the ability to rearrange the actin cytoskeleton and may also act as an oncosuppressor in osteosarcoma. This gene is found in the pseudoautosomal region of chromosomes X and Y and escapes X-chromosome inactivation. There is a related pseudogene located immediately adjacent to this locus. [provided by RefSeq, Mar 2016]","start":2691179,"end":2741309,"strand":1,"description":"CD99 molecule (Xg blood group) [Source:HGNC Symbol;Acc:HGNC:7082]"}, {"versioned_ensembl_gene_id":"ENSG00000224675.1","gene_symbol":"AC009227.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154435853,"end":154457438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272516.1","gene_symbol":"AL158211.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22332404,"end":22332987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230251.1","gene_symbol":"PHBP4","gene_name":"prohibitin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:8916]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418774","summary":null,"start":154286589,"end":154287425,"strand":1,"description":"prohibitin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:8916]"}, {"versioned_ensembl_gene_id":"ENSG00000271981.1","gene_symbol":"AL158211.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22332587,"end":22332981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162992.3","gene_symbol":"NEUROD1","gene_name":"neuronal differentiation 1 [Source:HGNC Symbol;Acc:HGNC:7762]","synonyms":"NEUROD,MODY6,bHLHa3,BHF-1,BETA2","biotype":"protein_coding","ncbi_id":"4760","summary":"This gene encodes a member of the NeuroD family of basic helix-loop-helix (bHLH) transcription factors. The protein forms heterodimers with other bHLH proteins and activates transcription of genes that contain a specific DNA sequence known as the E-box. It regulates expression of the insulin gene, and mutations in this gene result in type II diabetes mellitus. [provided by RefSeq, Jul 2008]","start":181673088,"end":181680876,"strand":-1,"description":"neuronal differentiation 1 [Source:HGNC Symbol;Acc:HGNC:7762]"}, {"versioned_ensembl_gene_id":"ENSG00000237042.1","gene_symbol":"MICG","gene_name":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352967","summary":null,"start":29812565,"end":29812696,"strand":-1,"description":"MHC class I polypeptide-related sequence G (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16802]"}, {"versioned_ensembl_gene_id":"ENSG00000236264.4","gene_symbol":"RPL26P30","gene_name":"ribosomal protein L26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36733]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"653147","summary":null,"start":2335132,"end":2335776,"strand":-1,"description":"ribosomal protein L26 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:36733]"}, {"versioned_ensembl_gene_id":"ENSG00000144278.14","gene_symbol":"GALNT13","gene_name":"polypeptide N-acetylgalactosaminyltransferase 13 [Source:HGNC Symbol;Acc:HGNC:23242]","synonyms":"KIAA1918,GalNAc-T13","biotype":"protein_coding","ncbi_id":"114805","summary":"The GALNT13 protein is a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAcT; EC 2.4.1.41) family, which initiate O-linked glycosylation of mucins (see MUC3A, MIM 158371) by the initial transfer of N-acetylgalactosamine (GalNAc) with an alpha-linkage to a serine or threonine residue.[supplied by OMIM, Apr 2004]","start":153871913,"end":154453849,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 13 [Source:HGNC Symbol;Acc:HGNC:23242]"}, {"versioned_ensembl_gene_id":"ENSG00000248635.1","gene_symbol":"AC147055.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68704600,"end":68712498,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238184.1","gene_symbol":"CD81-AS1","gene_name":"CD81 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49384]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927682","summary":null,"start":2328749,"end":2377992,"strand":-1,"description":"CD81 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49384]"}, {"versioned_ensembl_gene_id":"ENSG00000272366.1","gene_symbol":"AL158211.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22340377,"end":22340615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000018610.13","gene_symbol":"CXorf56","gene_name":"chromosome X open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:26239]","synonyms":"FLJ22965","biotype":"protein_coding","ncbi_id":"63932","summary":"While this gene is well-supported by transcript data, no functional information on its protein products is currently available. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":119538149,"end":119565408,"strand":-1,"description":"chromosome X open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:26239]"}, {"versioned_ensembl_gene_id":"ENSG00000239995.2","gene_symbol":"TPT1P11","gene_name":"tumor protein, translationally-controlled 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49302]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"102724868","summary":null,"start":48632856,"end":48633353,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49302]"}, {"versioned_ensembl_gene_id":"ENSG00000237051.8","gene_symbol":"GABBR1","gene_name":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]","synonyms":"hGB1a,GPRC3A","biotype":"protein_coding","ncbi_id":"2550","summary":"This gene encodes a receptor for gamma-aminobutyric acid (GABA), which is the main inhibitory neurotransmitter in the mammalian central nervous system. This receptor functions as a heterodimer with GABA(B) receptor 2. Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy. Alternative splicing generates multiple transcript variants, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jan 2016]","start":29555178,"end":29632716,"strand":-1,"description":"gamma-aminobutyric acid type B receptor subunit 1 [Source:HGNC Symbol;Acc:HGNC:4070]"}, {"versioned_ensembl_gene_id":"ENSG00000279956.1","gene_symbol":"AC073082.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":48632291,"end":48755724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237464.1","gene_symbol":"AL031663.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45487613,"end":45490248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250376.1","gene_symbol":"AC093720.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68784618,"end":68787474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249754.2","gene_symbol":"NDUFB4P9","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45257]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075211","summary":null,"start":140314163,"end":140314550,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:45257]"}, {"versioned_ensembl_gene_id":"ENSG00000255089.1","gene_symbol":"AC136475.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":321991,"end":322426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226401.3","gene_symbol":"AC006015.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63632608,"end":63636617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196951.10","gene_symbol":"SCOC-AS1","gene_name":"SCOC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50601]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100129858","summary":null,"start":140283724,"end":140373381,"strand":-1,"description":"SCOC antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50601]"}, {"versioned_ensembl_gene_id":"ENSG00000280513.1","gene_symbol":"LINC01262","gene_name":"long intergenic non-protein coding RNA 1262 [Source:NCBI gene;Acc:101928971]","synonyms":"TCONS_l2_00021807,RP11-462G22.1,TCONS_l2_00021807","biotype":"lincRNA","ncbi_id":"101928971","summary":null,"start":189669074,"end":189670954,"strand":1,"description":"long intergenic non-protein coding RNA 1262 [Source:NCBI gene;Acc:101928971]"}, {"versioned_ensembl_gene_id":"ENSG00000259395.1","gene_symbol":"AC087516.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36341739,"end":36344166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000110651.11","gene_symbol":"CD81","gene_name":"CD81 molecule [Source:HGNC Symbol;Acc:HGNC:1701]","synonyms":"TSPAN28,TAPA1,TAPA-1","biotype":"protein_coding","ncbi_id":"975","summary":"The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins. This protein appears to promote muscle cell fusion and support myotube maintenance. Also it may be involved in signal transduction. This gene is localized in the tumor-suppressor gene region and thus it is a candidate gene for malignancies. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":2376177,"end":2397419,"strand":1,"description":"CD81 molecule [Source:HGNC Symbol;Acc:HGNC:1701]"}, {"versioned_ensembl_gene_id":"ENSG00000226411.1","gene_symbol":"AC079355.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63699390,"end":63700441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242441.7","gene_symbol":"GTF2A1L","gene_name":"general transcription factor IIA subunit 1 like [Source:HGNC Symbol;Acc:HGNC:30727]","synonyms":"ALF","biotype":"protein_coding","ncbi_id":"11036","summary":"The assembly and stability of the RNA polymerase II transcription pre-initiation complex on a eukaryotic core promoter involve the effects of transcription factor IIA (TFIIA) on the interaction between TATA-binding protein (TBP) and DNA. This gene encodes a germ cell-specific counterpart of the large (alpha/beta) subunit of general transcription factor TFIIA that is able to stabilize the binding of TBP to DNA and may be uniquely important to testis biology. Alternative splicing for this locus has been observed and two variants, encoding distinct isoforms, have been identified. Co-transcription of this gene and the neighboring upstream gene generates a rare transcript (SALF), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Mar 2014]","start":48617798,"end":48733148,"strand":1,"description":"general transcription factor IIA subunit 1 like [Source:HGNC Symbol;Acc:HGNC:30727]"}, {"versioned_ensembl_gene_id":"ENSG00000241941.2","gene_symbol":"AC048341.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62658823,"end":62659225,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115232.13","gene_symbol":"ITGA4","gene_name":"integrin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6140]","synonyms":"CD49D","biotype":"protein_coding","ncbi_id":"3676","summary":"The gene encodes a member of the integrin alpha chain family of proteins. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain that function in cell surface adhesion and signaling. The encoded preproprotein is proteolytically processed to generate light and heavy chains that comprise the alpha 4 subunit. This subunit associates with a beta 1 or beta 7 subunit to form an integrin that may play a role in cell motility and migration. This integrin is a therapeutic target for the treatment of multiple sclerosis, Crohn's disease and inflammatory bowel disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":181457202,"end":181536187,"strand":1,"description":"integrin subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:6140]"}, {"versioned_ensembl_gene_id":"ENSG00000242285.1","gene_symbol":"RPL6P8","gene_name":"ribosomal protein L6 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37044]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100133100","summary":null,"start":160584945,"end":160585787,"strand":1,"description":"ribosomal protein L6 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:37044]"}, {"versioned_ensembl_gene_id":"ENSG00000100023.18","gene_symbol":"PPIL2","gene_name":"peptidylprolyl isomerase like 2 [Source:HGNC Symbol;Acc:HGNC:9261]","synonyms":"UBOX7,Cyp-60,CYC4","biotype":"protein_coding","ncbi_id":"23759","summary":"This gene is a member of the cyclophilin family of peptidylprolyl isomerases. The cyclophilins are a highly conserved ubiquitous family, members of which play an important role in protein folding, immunosuppression by cyclosporin A, and infection of HIV-1 virions. This protein interacts with the proteinase inhibitor eglin c and is localized in the nucleus. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015]","start":21666009,"end":21700015,"strand":1,"description":"peptidylprolyl isomerase like 2 [Source:HGNC Symbol;Acc:HGNC:9261]"}, {"versioned_ensembl_gene_id":"ENSG00000230657.6","gene_symbol":"PRB4","gene_name":"proline rich protein BstNI subfamily 4 [Source:HGNC Symbol;Acc:HGNC:9340]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5545","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Small\" allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015]","start":11307083,"end":11310435,"strand":-1,"description":"proline rich protein BstNI subfamily 4 [Source:HGNC Symbol;Acc:HGNC:9340]"}, {"versioned_ensembl_gene_id":"ENSG00000179674.3","gene_symbol":"ARL14","gene_name":"ADP ribosylation factor like GTPase 14 [Source:HGNC Symbol;Acc:HGNC:22974]","synonyms":"FLJ22595,ARF7","biotype":"protein_coding","ncbi_id":"80117","summary":null,"start":160677159,"end":160678452,"strand":1,"description":"ADP ribosylation factor like GTPase 14 [Source:HGNC Symbol;Acc:HGNC:22974]"}, {"versioned_ensembl_gene_id":"ENSG00000232825.1","gene_symbol":"AL445433.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99004276,"end":99148852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117598.11","gene_symbol":"PLPPR5","gene_name":"phospholipid phosphatase related 5 [Source:HGNC Symbol;Acc:HGNC:31703]","synonyms":"PRG5,PAP2D,PAP2,LPPR5","biotype":"protein_coding","ncbi_id":"163404","summary":"The protein encoded by this gene is a type 2 member of the phosphatidic acid phosphatase (PAP) family. All type 2 members of this protein family contain 6 transmembrane regions, and a consensus N-glycosylation site. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":98890245,"end":99005032,"strand":-1,"description":"phospholipid phosphatase related 5 [Source:HGNC Symbol;Acc:HGNC:31703]"}, {"versioned_ensembl_gene_id":"ENSG00000169877.9","gene_symbol":"AHSP","gene_name":"alpha hemoglobin stabilizing protein [Source:HGNC Symbol;Acc:HGNC:18075]","synonyms":"ERAF,EDRF","biotype":"protein_coding","ncbi_id":"51327","summary":"This gene encodes a molecular chaperone which binds specifically to free alpha-globin and is involved in hemoglobin assembly. The encoded protein binds to monomeric alpha-globin until it has been transferred to beta-globin to form a heterodimer, which in turn binds to another heterodimer to form the stable tetrameric hemoglobin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":31527864,"end":31528803,"strand":1,"description":"alpha hemoglobin stabilizing protein [Source:HGNC Symbol;Acc:HGNC:18075]"}, {"versioned_ensembl_gene_id":"ENSG00000253112.1","gene_symbol":"AC102945.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30596914,"end":30597532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146215.13","gene_symbol":"CRIP3","gene_name":"cysteine rich protein 3 [Source:HGNC Symbol;Acc:HGNC:17751]","synonyms":"TLP-A,TLP,bA480N24.2","biotype":"protein_coding","ncbi_id":"401262","summary":null,"start":43299710,"end":43308797,"strand":-1,"description":"cysteine rich protein 3 [Source:HGNC Symbol;Acc:HGNC:17751]"}, {"versioned_ensembl_gene_id":"ENSG00000257681.1","gene_symbol":"AC025265.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103746315,"end":103768858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280853.1","gene_symbol":"AF250324.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189714467,"end":189715076,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259737.6","gene_symbol":"AC087516.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36438972,"end":36471016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251236.1","gene_symbol":"AC021146.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68813995,"end":68814727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257550.1","gene_symbol":"AC023509.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53513984,"end":53517608,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227034.1","gene_symbol":"AL445433.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99008218,"end":99008474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281377.1","gene_symbol":"LINC01596","gene_name":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]","synonyms":"TCONS_00007705","biotype":"lincRNA","ncbi_id":"105377617","summary":null,"start":189892101,"end":189895454,"strand":1,"description":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]"}, {"versioned_ensembl_gene_id":"ENSG00000174697.4","gene_symbol":"LEP","gene_name":"leptin [Source:HGNC Symbol;Acc:HGNC:6553]","synonyms":"OBS,OB","biotype":"protein_coding","ncbi_id":"3952","summary":"This gene encodes a protein that is secreted by white adipocytes into the circulation and plays a major role in the regulation of energy homeostasis. Circulating leptin binds to the leptin receptor in the brain, which activates downstream signaling pathways that inhibit feeding and promote energy expenditure. This protein also has several endocrine functions, and is involved in the regulation of immune and inflammatory responses, hematopoiesis, angiogenesis, reproduction, bone formation and wound healing. Mutations in this gene and its regulatory regions cause severe obesity and morbid obesity with hypogonadism in human patients. A mutation in this gene has also been linked to type 2 diabetes mellitus development. [provided by RefSeq, Aug 2017]","start":128241284,"end":128257628,"strand":1,"description":"leptin [Source:HGNC Symbol;Acc:HGNC:6553]"}, {"versioned_ensembl_gene_id":"ENSG00000257766.1","gene_symbol":"AC025265.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103668575,"end":103669406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000073910.20","gene_symbol":"FRY","gene_name":"FRY microtubule binding protein [Source:HGNC Symbol;Acc:HGNC:20367]","synonyms":"bA37E23.1,13CDNA73,CG003,C13orf14","biotype":"protein_coding","ncbi_id":"10129","summary":null,"start":32031300,"end":32299122,"strand":1,"description":"FRY microtubule binding protein [Source:HGNC Symbol;Acc:HGNC:20367]"}, {"versioned_ensembl_gene_id":"ENSG00000233056.2","gene_symbol":"ERVH48-1","gene_name":"endogenous retrovirus group 48 member 1 [Source:HGNC Symbol;Acc:HGNC:17216]","synonyms":"NDUFV3-AS1,C21orf105","biotype":"lincRNA","ncbi_id":"90625","summary":"Many different endogenous retrovirus families are expressed in normal placental tissue at high levels, suggesting that endogenous retroviruses are functionally important in reproduction. This gene is part of an endogenous retrovirus provirus that has placenta specific expression. The protein encoded has the characteristics of a retroviral envelope protein but is truncated and lacks the transmembrane domain. The protein inhibits cell fusion by competing with syncytin-1 for binding to a cell receptor. [provided by RefSeq, May 2015]","start":42916803,"end":42925646,"strand":-1,"description":"endogenous retrovirus group 48 member 1 [Source:HGNC Symbol;Acc:HGNC:17216]"}, {"versioned_ensembl_gene_id":"ENSG00000232306.2","gene_symbol":"AC012485.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":238295392,"end":238300620,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257737.1","gene_symbol":"AC025265.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103654780,"end":103657995,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225057.2","gene_symbol":"AC012485.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":238231684,"end":238255633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117115.12","gene_symbol":"PADI2","gene_name":"peptidyl arginine deiminase 2 [Source:HGNC Symbol;Acc:HGNC:18341]","synonyms":"PDI2,KIAA0994","biotype":"protein_coding","ncbi_id":"11240","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type II enzyme is the most widely expressed family member. Known substrates for this enzyme include myelin basic protein in the central nervous system and vimentin in skeletal muscle and macrophages. This enzyme is thought to play a role in the onset and progression of neurodegenerative human disorders, including Alzheimer disease and multiple sclerosis, and it has also been implicated in glaucoma pathogenesis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17066761,"end":17119435,"strand":-1,"description":"peptidyl arginine deiminase 2 [Source:HGNC Symbol;Acc:HGNC:18341]"}, {"versioned_ensembl_gene_id":"ENSG00000136011.14","gene_symbol":"STAB2","gene_name":"stabilin 2 [Source:HGNC Symbol;Acc:HGNC:18629]","synonyms":"STAB-2,SCARH1,HARE,FELL,FEEL-2,DKFZP434E0321","biotype":"protein_coding","ncbi_id":"55576","summary":"This gene encodes a large, transmembrane receptor protein which may function in angiogenesis, lymphocyte homing, cell adhesion, or receptor scavenging. The protein contains 7 fasciclin, 15 epidermal growth factor (EGF)-like, and 2 laminin-type EGF-like domains as well as a C-type lectin-like hyaluronan-binding Link module. The protein is primarily expressed on sinusoidal endothelial cells of liver, spleen, and lymph node. The receptor has been shown to bind and endocytose ligands such as hyaluronan, low density lipoprotein, Gram-positive and Gram-negative bacteria, and advanced glycosylation end products. Supporting its possible role as a scavenger receptor, the protein has been shown to cycle between the plasma membrane and lysosomes. [provided by RefSeq, Jul 2008]","start":103587273,"end":103766727,"strand":1,"description":"stabilin 2 [Source:HGNC Symbol;Acc:HGNC:18629]"}, {"versioned_ensembl_gene_id":"ENSG00000132326.11","gene_symbol":"PER2","gene_name":"period circadian clock 2 [Source:HGNC Symbol;Acc:HGNC:8846]","synonyms":"KIAA0347","biotype":"protein_coding","ncbi_id":"8864","summary":"This gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene may increase the risk of getting certain cancers and have been linked to sleep disorders. [provided by RefSeq, Jan 2014]","start":238244038,"end":238290102,"strand":-1,"description":"period circadian clock 2 [Source:HGNC Symbol;Acc:HGNC:8846]"}, {"versioned_ensembl_gene_id":"ENSG00000136718.9","gene_symbol":"IMP4","gene_name":"IMP4, U3 small nucleolar ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:30856]","synonyms":"BXDC4,MGC19606","biotype":"protein_coding","ncbi_id":"92856","summary":"The protein encoded by this gene, along with IMP3 and MPP10, is part of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex. This complex is necessary for the early cleavage steps of pre-18S ribosomal RNA processing. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":130342225,"end":130347810,"strand":1,"description":"IMP4, U3 small nucleolar ribonucleoprotein [Source:HGNC Symbol;Acc:HGNC:30856]"}, {"versioned_ensembl_gene_id":"ENSG00000224100.1","gene_symbol":"AP001630.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42964639,"end":42965363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249896.2","gene_symbol":"LINC02495","gene_name":"long intergenic non-protein coding RNA 2495 [Source:HGNC Symbol;Acc:HGNC:27728]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285484","summary":null,"start":6200733,"end":6239937,"strand":1,"description":"long intergenic non-protein coding RNA 2495 [Source:HGNC Symbol;Acc:HGNC:27728]"}, {"versioned_ensembl_gene_id":"ENSG00000271466.1","gene_symbol":"CICP24","gene_name":"capicua transcriptional repressor pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:48831]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996387","summary":null,"start":63768257,"end":63771047,"strand":-1,"description":"capicua transcriptional repressor pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:48831]"}, {"versioned_ensembl_gene_id":"ENSG00000273402.1","gene_symbol":"AC004908.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":237045,"end":237669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251408.1","gene_symbol":"AC113615.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6202328,"end":6206649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272812.1","gene_symbol":"AC004908.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":233119,"end":233692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260572.1","gene_symbol":"AC069224.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160753428,"end":160755142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281610.1","gene_symbol":"HSP90AA4P","gene_name":"heat shock protein 90 alpha family class A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:5255]","synonyms":"HSPCAL2","biotype":"transcribed_processed_pseudogene","ncbi_id":"3323","summary":null,"start":189472965,"end":189475192,"strand":1,"description":"heat shock protein 90 alpha family class A member 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:5255]"}, {"versioned_ensembl_gene_id":"ENSG00000139574.8","gene_symbol":"NPFF","gene_name":"neuropeptide FF-amide peptide precursor [Source:HGNC Symbol;Acc:HGNC:7901]","synonyms":"FMRFAL","biotype":"protein_coding","ncbi_id":"8620","summary":"This gene encodes a member of the FMRFamide related peptide (FARP) family of neuropeptides. The encoded preproprotein is proteolytically processed to generate multiple amidated peptides. These peptides may play a role in the regulation of heart rate and blood pressure and the modulation of morphine-induced antinociception. Patients with hypertension exhibit decreased expression of the encoded protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":53506690,"end":53507638,"strand":-1,"description":"neuropeptide FF-amide peptide precursor [Source:HGNC Symbol;Acc:HGNC:7901]"}, {"versioned_ensembl_gene_id":"ENSG00000270500.1","gene_symbol":"COX6CP4","gene_name":"cytochrome c oxidase subunit 6C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288892","summary":null,"start":36571985,"end":36572212,"strand":1,"description":"cytochrome c oxidase subunit 6C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32374]"}, {"versioned_ensembl_gene_id":"ENSG00000143420.18","gene_symbol":"ENSA","gene_name":"endosulfine alpha [Source:HGNC Symbol;Acc:HGNC:3360]","synonyms":"MGC8394,MGC78563,MGC4319,ARPP-19e","biotype":"protein_coding","ncbi_id":"2029","summary":"The protein encoded by this gene belongs to a highly conserved cAMP-regulated phosphoprotein (ARPP) family. This protein was identified as an endogenous ligand for the sulfonylurea receptor, ABCC8/SUR1. ABCC8 is the regulatory subunit of the ATP-sensitive potassium (KATP) channel, which is located on the plasma membrane of pancreatic beta cells and plays a key role in the control of insulin release from pancreatic beta cells. This protein is thought to be an endogenous regulator of KATP channels. In vitro studies have demonstrated that this protein modulates insulin secretion through the interaction with KATP channel, and this gene has been proposed as a candidate gene for type 2 diabetes. At least eight alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":150600851,"end":150629612,"strand":-1,"description":"endosulfine alpha [Source:HGNC Symbol;Acc:HGNC:3360]"}, {"versioned_ensembl_gene_id":"ENSG00000273954.1","gene_symbol":"LINC01194","gene_name":"long intergenic non-protein coding RNA 1194 [Source:HGNC Symbol;Acc:HGNC:37171]","synonyms":"TAG,CT49","biotype":"lincRNA","ncbi_id":"404663","summary":null,"start":12686551,"end":12731442,"strand":1,"description":"long intergenic non-protein coding RNA 1194 [Source:HGNC Symbol;Acc:HGNC:37171]"}, {"versioned_ensembl_gene_id":"ENSG00000231952.3","gene_symbol":"DPY19L1P2","gene_name":"DPY19L1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22851]","synonyms":"THC1072510","biotype":"unprocessed_pseudogene","ncbi_id":"102724668","summary":null,"start":32812757,"end":32838570,"strand":1,"description":"DPY19L1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:22851]"}, {"versioned_ensembl_gene_id":"ENSG00000215595.1","gene_symbol":"C20orf202","gene_name":"chromosome 20 open reading frame 202 [Source:HGNC Symbol;Acc:HGNC:37254]","synonyms":null,"biotype":"protein_coding","ncbi_id":"400831","summary":null,"start":1203454,"end":1208274,"strand":1,"description":"chromosome 20 open reading frame 202 [Source:HGNC Symbol;Acc:HGNC:37254]"}, {"versioned_ensembl_gene_id":"ENSG00000162040.6","gene_symbol":"HS3ST6","gene_name":"heparan sulfate-glucosamine 3-sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:14178]","synonyms":"HS3ST5","biotype":"protein_coding","ncbi_id":"64711","summary":null,"start":1911463,"end":1918440,"strand":-1,"description":"heparan sulfate-glucosamine 3-sulfotransferase 6 [Source:HGNC Symbol;Acc:HGNC:14178]"}, {"versioned_ensembl_gene_id":"ENSG00000230299.1","gene_symbol":"AC093162.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85262144,"end":85262267,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281703.1","gene_symbol":"AC245690.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69930714,"end":69941207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278019.2","gene_symbol":"AC245690.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69910279,"end":69916203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152284.4","gene_symbol":"TCF7L1","gene_name":"transcription factor 7 like 1 [Source:HGNC Symbol;Acc:HGNC:11640]","synonyms":"TCF3","biotype":"protein_coding","ncbi_id":"83439","summary":"This gene encodes a member of the T cell factor/lymphoid enhancer factor family of transcription factors. These transcription factors are activated by beta catenin, mediate the Wnt signaling pathway and are antagonized by the transforming growth factor beta signaling pathway. The encoded protein contains a high mobility group-box DNA binding domain and participates in the regulation of cell cycle genes and cellular senescence. [provided by RefSeq, Nov 2010]","start":85133410,"end":85310388,"strand":1,"description":"transcription factor 7 like 1 [Source:HGNC Symbol;Acc:HGNC:11640]"}, {"versioned_ensembl_gene_id":"ENSG00000280638.1","gene_symbol":"CDH12P2","gene_name":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]","synonyms":"CDH12P,C41-CAD","biotype":"unprocessed_pseudogene","ncbi_id":"1011","summary":null,"start":70005540,"end":70005841,"strand":-1,"description":"cadherin 12 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:1752]"}, {"versioned_ensembl_gene_id":"ENSG00000133104.12","gene_symbol":"SPART","gene_name":"spartin [Source:HGNC Symbol;Acc:HGNC:18514]","synonyms":"TAHCCP1,SPG20,KIAA0610","biotype":"protein_coding","ncbi_id":"23111","summary":"This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]","start":36301638,"end":36370180,"strand":-1,"description":"spartin [Source:HGNC Symbol;Acc:HGNC:18514]"}, {"versioned_ensembl_gene_id":"ENSG00000223587.1","gene_symbol":"LINC01986","gene_name":"long intergenic non-protein coding RNA 1986 [Source:HGNC Symbol;Acc:HGNC:52817]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723448","summary":null,"start":23757,"end":24501,"strand":1,"description":"long intergenic non-protein coding RNA 1986 [Source:HGNC Symbol;Acc:HGNC:52817]"}, {"versioned_ensembl_gene_id":"ENSG00000237303.2","gene_symbol":"HIGD1AP8","gene_name":"HIG1 hypoxia inducible domain family member 1A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43003]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874451","summary":null,"start":11481383,"end":11481656,"strand":1,"description":"HIG1 hypoxia inducible domain family member 1A pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:43003]"}, {"versioned_ensembl_gene_id":"ENSG00000251655.6","gene_symbol":"PRB1","gene_name":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]","synonyms":"PRB1M,PRB1L,PMS,PMF,PM","biotype":"protein_coding","ncbi_id":"5542","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the \"Medium\" allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015]","start":11351823,"end":11395566,"strand":-1,"description":"proline rich protein BstNI subfamily 1 [Source:HGNC Symbol;Acc:HGNC:9337]"}, {"versioned_ensembl_gene_id":"ENSG00000215388.3","gene_symbol":"ACTG1P3","gene_name":"actin gamma 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:148]","synonyms":"ACTGP3","biotype":"processed_pseudogene","ncbi_id":"75","summary":null,"start":1160584,"end":1161697,"strand":1,"description":"actin gamma 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:148]"}, {"versioned_ensembl_gene_id":"ENSG00000224918.1","gene_symbol":"AC066595.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":53348,"end":54346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125895.5","gene_symbol":"TMEM74B","gene_name":"transmembrane protein 74B [Source:HGNC Symbol;Acc:HGNC:15893]","synonyms":"FLJ11190,C20orf46","biotype":"protein_coding","ncbi_id":"55321","summary":null,"start":1180561,"end":1185415,"strand":-1,"description":"transmembrane protein 74B [Source:HGNC Symbol;Acc:HGNC:15893]"}, {"versioned_ensembl_gene_id":"ENSG00000254037.2","gene_symbol":"AC021733.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119480279,"end":119480775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109181.11","gene_symbol":"UGT2B10","gene_name":"UDP glucuronosyltransferase family 2 member B10 [Source:HGNC Symbol;Acc:HGNC:12544]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7365","summary":null,"start":68815993,"end":68831196,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B10 [Source:HGNC Symbol;Acc:HGNC:12544]"}, {"versioned_ensembl_gene_id":"ENSG00000244257.5","gene_symbol":"PKD1P1","gene_name":"polycystin 1, transient receptor potential channel interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30065]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"339044","summary":null,"start":16310341,"end":16334190,"strand":1,"description":"polycystin 1, transient receptor potential channel interacting pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30065]"}, {"versioned_ensembl_gene_id":"ENSG00000276026.1","gene_symbol":"AL031665.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1117847,"end":1118450,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258722.2","gene_symbol":"CKAP2P1","gene_name":"cytoskeleton associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49923]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420763","summary":null,"start":21110295,"end":21113472,"strand":-1,"description":"cytoskeleton associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49923]"}, {"versioned_ensembl_gene_id":"ENSG00000223431.1","gene_symbol":"MTND6P21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39639]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873332","summary":null,"start":44472895,"end":44473739,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:39639]"}, {"versioned_ensembl_gene_id":"ENSG00000165621.8","gene_symbol":"OXGR1","gene_name":"oxoglutarate receptor 1 [Source:HGNC Symbol;Acc:HGNC:4531]","synonyms":"GPR99,GPR80,aKGR,P2Y15,P2RY15","biotype":"protein_coding","ncbi_id":"27199","summary":"This gene encodes a G protein-coupled receptor (GPCR) that belongs to the oxoglutarate receptor family within the GPCR superfamily. The encoded protein is activated by the citric acid intermediate, oxoglutarate, as well as several cysteinyl leukotrienes, including leukotrienes E4, C4 and D4, which are implicated in many inflammatory disorders. In mice, a knock-out of this gene leads to middle ear inflammation, changes in the mucosal epithelium, and an increase in fluid behind the eardrum, and is associated with hearing loss. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":96985719,"end":96994730,"strand":-1,"description":"oxoglutarate receptor 1 [Source:HGNC Symbol;Acc:HGNC:4531]"}, {"versioned_ensembl_gene_id":"ENSG00000277429.4","gene_symbol":"SERF1B","gene_name":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]","synonyms":"H4F5C,FAM2B","biotype":"protein_coding","ncbi_id":"728492","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008]","start":70045915,"end":70063796,"strand":1,"description":"small EDRK-rich factor 1B [Source:HGNC Symbol;Acc:HGNC:10756]"}, {"versioned_ensembl_gene_id":"ENSG00000274269.1","gene_symbol":"AL031665.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":1186092,"end":1207036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225064.1","gene_symbol":"LINC01802","gene_name":"long intergenic non-protein coding RNA 1802 [Source:HGNC Symbol;Acc:HGNC:52591]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373852","summary":null,"start":207260445,"end":207270690,"strand":1,"description":"long intergenic non-protein coding RNA 1802 [Source:HGNC Symbol;Acc:HGNC:52591]"}, {"versioned_ensembl_gene_id":"ENSG00000248571.1","gene_symbol":"AC106882.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152666368,"end":152670107,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170006.11","gene_symbol":"TMEM154","gene_name":"transmembrane protein 154 [Source:HGNC Symbol;Acc:HGNC:26489]","synonyms":"FLJ32028","biotype":"protein_coding","ncbi_id":"201799","summary":null,"start":152618632,"end":152680165,"strand":-1,"description":"transmembrane protein 154 [Source:HGNC Symbol;Acc:HGNC:26489]"}, {"versioned_ensembl_gene_id":"ENSG00000118260.14","gene_symbol":"CREB1","gene_name":"cAMP responsive element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2345]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1385","summary":"This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. This protein binds as a homodimer to the cAMP-responsive element, an octameric palindrome. The protein is phosphorylated by several protein kinases, and induces transcription of genes in response to hormonal stimulation of the cAMP pathway. Alternate splicing of this gene results in several transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":207529737,"end":207603431,"strand":1,"description":"cAMP responsive element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:2345]"}, {"versioned_ensembl_gene_id":"ENSG00000231983.1","gene_symbol":"LINC00415","gene_name":"long intergenic non-protein coding RNA 415 [Source:HGNC Symbol;Acc:HGNC:42748]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984009","summary":null,"start":26052276,"end":26053385,"strand":-1,"description":"long intergenic non-protein coding RNA 415 [Source:HGNC Symbol;Acc:HGNC:42748]"}, {"versioned_ensembl_gene_id":"ENSG00000256116.1","gene_symbol":"AP001453.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64229214,"end":64234352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175793.11","gene_symbol":"SFN","gene_name":"stratifin [Source:HGNC Symbol;Acc:HGNC:10773]","synonyms":"YWHAS","biotype":"protein_coding","ncbi_id":"2810","summary":"This gene encodes a cell cycle checkpoint protein. The encoded protein binds to translation and initiation factors and functions as a regulator of mitotic translation. In response to DNA damage this protein plays a role in preventing DNA errors during mitosis. [provided by RefSeq, Aug 2017]","start":26863138,"end":26864457,"strand":1,"description":"stratifin [Source:HGNC Symbol;Acc:HGNC:10773]"}, {"versioned_ensembl_gene_id":"ENSG00000260940.1","gene_symbol":"AL109741.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":101243158,"end":101243749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235009.1","gene_symbol":"LINC01883","gene_name":"long intergenic non-protein coding RNA 1883 [Source:HGNC Symbol;Acc:HGNC:52702]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996902","summary":null,"start":38431294,"end":38433573,"strand":1,"description":"long intergenic non-protein coding RNA 1883 [Source:HGNC Symbol;Acc:HGNC:52702]"}, {"versioned_ensembl_gene_id":"ENSG00000110011.13","gene_symbol":"DNAJC4","gene_name":"DnaJ heat shock protein family (Hsp40) member C4 [Source:HGNC Symbol;Acc:HGNC:5271]","synonyms":"MCG18,HSPF2","biotype":"protein_coding","ncbi_id":"3338","summary":null,"start":64230278,"end":64234286,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C4 [Source:HGNC Symbol;Acc:HGNC:5271]"}, {"versioned_ensembl_gene_id":"ENSG00000228399.1","gene_symbol":"AL109741.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101256274,"end":101256616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198176.12","gene_symbol":"TFDP1","gene_name":"transcription factor Dp-1 [Source:HGNC Symbol;Acc:HGNC:11749]","synonyms":"DRTF1,DP1,Dp-1,DILC","biotype":"protein_coding","ncbi_id":"7027","summary":"This gene encodes a member of a family of transcription factors that heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. The encoded protein functions as part of this complex to control the transcriptional activity of numerous genes involved in cell cycle progression from G1 to S phase. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 1, 15, and X.[provided by RefSeq, Jan 2009]","start":113584721,"end":113641470,"strand":1,"description":"transcription factor Dp-1 [Source:HGNC Symbol;Acc:HGNC:11749]"}, {"versioned_ensembl_gene_id":"ENSG00000173810.9","gene_symbol":"PPIAP7","gene_name":"peptidylprolyl isomerase A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:9270]","synonyms":"PPIP7","biotype":"processed_pseudogene","ncbi_id":"5489","summary":null,"start":101270875,"end":101271363,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:9270]"}, {"versioned_ensembl_gene_id":"ENSG00000183889.12","gene_symbol":"AC138969.1","gene_name":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16317444,"end":16350590,"strand":1,"description":"nuclear pore complex-interacting protein family member A5 isoform 2 [Source:RefSeq peptide;Acc:NP_001338129]"}, {"versioned_ensembl_gene_id":"ENSG00000231367.5","gene_symbol":"AC011247.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38406719,"end":38515740,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224747.1","gene_symbol":"MTCYBP21","gene_name":"mitochondrially encoded cytochrome b pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51977]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075260","summary":null,"start":44469929,"end":44472516,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51977]"}, {"versioned_ensembl_gene_id":"ENSG00000237068.1","gene_symbol":"RPL5P2","gene_name":"ribosomal protein L5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16568]","synonyms":"dJ461P17.5","biotype":"processed_pseudogene","ncbi_id":"140749","summary":null,"start":45490818,"end":45491671,"strand":-1,"description":"ribosomal protein L5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16568]"}, {"versioned_ensembl_gene_id":"ENSG00000278654.1","gene_symbol":"AC007450.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11500499,"end":11501022,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282735.1","gene_symbol":"KIAA0355","gene_name":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9710","summary":null,"start":34351514,"end":34355586,"strand":1,"description":"KIAA0355 [Source:HGNC Symbol;Acc:HGNC:29016]"}, {"versioned_ensembl_gene_id":"ENSG00000283635.1","gene_symbol":"AC012485.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":238289127,"end":238300185,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000121335.11","gene_symbol":"PRB2","gene_name":"proline rich protein BstNI subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9338]","synonyms":"Ps,PRPPRB1,cP7","biotype":"protein_coding","ncbi_id":"653247","summary":"This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats, polymorphic cleavage sites and polymorphic stop codons have been identified. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Oct 2015]","start":11391540,"end":11501041,"strand":-1,"description":"proline rich protein BstNI subfamily 2 [Source:HGNC Symbol;Acc:HGNC:9338]"}, {"versioned_ensembl_gene_id":"ENSG00000144485.10","gene_symbol":"HES6","gene_name":"hes family bHLH transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:18254]","synonyms":"bHLHb41","biotype":"protein_coding","ncbi_id":"55502","summary":"This gene encodes a member of a subfamily of basic helix-loop-helix transcription repressors that have homology to the Drosophila enhancer of split genes. Members of this gene family regulate cell differentiation in numerous cell types. The protein encoded by this gene functions as a cofactor, interacting with other transcription factors through a tetrapeptide domain in its C-terminus. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Dec 2008]","start":238238267,"end":238240662,"strand":-1,"description":"hes family bHLH transcription factor 6 [Source:HGNC Symbol;Acc:HGNC:18254]"}, {"versioned_ensembl_gene_id":"ENSG00000178107.2","gene_symbol":"AL161668.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21108043,"end":21116703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101446.7","gene_symbol":"SPINT3","gene_name":"serine peptidase inhibitor, Kunitz type 3 [Source:HGNC Symbol;Acc:HGNC:11248]","synonyms":"HKIB9","biotype":"protein_coding","ncbi_id":"10816","summary":null,"start":45512461,"end":45515624,"strand":-1,"description":"serine peptidase inhibitor, Kunitz type 3 [Source:HGNC Symbol;Acc:HGNC:11248]"}, {"versioned_ensembl_gene_id":"ENSG00000226698.1","gene_symbol":"AL034380.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26876133,"end":26878245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277368.1","gene_symbol":"AL138966.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26222191,"end":26222654,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142751.14","gene_symbol":"GPN2","gene_name":"GPN-loop GTPase 2 [Source:HGNC Symbol;Acc:HGNC:25513]","synonyms":"ATPBD1B,FLJ10349","biotype":"protein_coding","ncbi_id":"54707","summary":null,"start":26876133,"end":26890297,"strand":-1,"description":"GPN-loop GTPase 2 [Source:HGNC Symbol;Acc:HGNC:25513]"}, {"versioned_ensembl_gene_id":"ENSG00000213553.4","gene_symbol":"RPLP0P6","gene_name":"ribosomal protein lateral stalk subunit P0 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36404]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"220717","summary":null,"start":38481851,"end":38482804,"strand":1,"description":"ribosomal protein lateral stalk subunit P0 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36404]"}, {"versioned_ensembl_gene_id":"ENSG00000127870.16","gene_symbol":"RNF6","gene_name":"ring finger protein 6 [Source:HGNC Symbol;Acc:HGNC:10069]","synonyms":"DKFZp686P0776","biotype":"protein_coding","ncbi_id":"6049","summary":"The protein encoded by this gene contains a RING-H2 finger motif. Deletions and mutations in this gene were detected in esophageal squamous cell carcinoma (ESCC), suggesting that this protein may be a potential tumor suppressor. Studies of the mouse counterpart suggested a role of this protein in the transcription regulation that controls germinal differentiation. Multiple alternatively spliced transcript variants encoding the same protein are observed. [provided by RefSeq, Jul 2008]","start":26132115,"end":26222493,"strand":-1,"description":"ring finger protein 6 [Source:HGNC Symbol;Acc:HGNC:10069]"}, {"versioned_ensembl_gene_id":"ENSG00000169327.5","gene_symbol":"OR5AU1","gene_name":"olfactory receptor family 5 subfamily AU member 1 [Source:HGNC Symbol;Acc:HGNC:15362]","synonyms":null,"biotype":"protein_coding","ncbi_id":"390445","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21148370,"end":21159060,"strand":-1,"description":"olfactory receptor family 5 subfamily AU member 1 [Source:HGNC Symbol;Acc:HGNC:15362]"}, {"versioned_ensembl_gene_id":"ENSG00000231671.1","gene_symbol":"LINC01307","gene_name":"long intergenic non-protein coding RNA 1307 [Source:HGNC Symbol;Acc:HGNC:50494]","synonyms":"RP11-157N3.1","biotype":"lincRNA","ncbi_id":"104355286","summary":null,"start":101323337,"end":101390303,"strand":1,"description":"long intergenic non-protein coding RNA 1307 [Source:HGNC Symbol;Acc:HGNC:50494]"}, {"versioned_ensembl_gene_id":"ENSG00000229002.1","gene_symbol":"AC246785.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144472535,"end":144474790,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279782.1","gene_symbol":"PPIAL4F","gene_name":"peptidylprolyl isomerase A like 4F [Source:HGNC Symbol;Acc:HGNC:33999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728945","summary":null,"start":144592868,"end":144593527,"strand":1,"description":"peptidylprolyl isomerase A like 4F [Source:HGNC Symbol;Acc:HGNC:33999]"}, {"versioned_ensembl_gene_id":"ENSG00000282746.1","gene_symbol":"AC010504.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":34358485,"end":34359412,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231134.1","gene_symbol":"TCF7L1-IT1","gene_name":"TCF7L1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41388]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874334","summary":null,"start":85186409,"end":85187253,"strand":1,"description":"TCF7L1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41388]"}, {"versioned_ensembl_gene_id":"ENSG00000227397.1","gene_symbol":"AC079355.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63789909,"end":63790098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280275.1","gene_symbol":"Z82209.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":127392760,"end":127394771,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236574.1","gene_symbol":"AC092634.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63843314,"end":63843505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274631.1","gene_symbol":"AL662814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127623410,"end":127623530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183298.5","gene_symbol":"RPSAP19","gene_name":"ribosomal protein SA pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36508]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730029","summary":null,"start":101786340,"end":101787219,"strand":-1,"description":"ribosomal protein SA pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36508]"}, {"versioned_ensembl_gene_id":"ENSG00000249148.2","gene_symbol":"AC006445.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13631820,"end":13632599,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188021.8","gene_symbol":"UBQLN2","gene_name":"ubiquilin 2 [Source:HGNC Symbol;Acc:HGNC:12509]","synonyms":"PLIC2,PLIC-2,N4BP4,LIC-2,Dsk2,CHAP1/DSK2,Chap1,RIHFB2157","biotype":"protein_coding","ncbi_id":"29978","summary":"This gene encodes an ubiquitin-like protein (ubiquilin) that shares high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain a N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically associate with both proteasomes and ubiquitin ligases; and thus, are thought to functionally link the ubiquitination machinery to the proteasome to affect in vivo protein degradation. This ubiquilin has also been shown to bind the ATPase domain of the Hsp70-like Stch protein. [provided by RefSeq, Oct 2009]","start":56563639,"end":56567868,"strand":1,"description":"ubiquilin 2 [Source:HGNC Symbol;Acc:HGNC:12509]"}, {"versioned_ensembl_gene_id":"ENSG00000226715.2","gene_symbol":"LINC01709","gene_name":"long intergenic non-protein coding RNA 1709 [Source:HGNC Symbol;Acc:HGNC:52497]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378872","summary":null,"start":101639548,"end":101787572,"strand":1,"description":"long intergenic non-protein coding RNA 1709 [Source:HGNC Symbol;Acc:HGNC:52497]"}, {"versioned_ensembl_gene_id":"ENSG00000159261.10","gene_symbol":"CLDN14","gene_name":"claudin 14 [Source:HGNC Symbol;Acc:HGNC:2035]","synonyms":"DFNB29","biotype":"protein_coding","ncbi_id":"23562","summary":"Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. The encoded protein also binds specifically to the WW domain of Yes-associated protein. Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness. It is also reported that four synonymous variants in this gene are associated with kidney stones and reduced bone mineral density. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2010]","start":36460621,"end":36576569,"strand":-1,"description":"claudin 14 [Source:HGNC Symbol;Acc:HGNC:2035]"}, {"versioned_ensembl_gene_id":"ENSG00000260683.1","gene_symbol":"AL591643.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127660631,"end":127662530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225451.1","gene_symbol":"AC092634.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63876341,"end":63877350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235274.1","gene_symbol":"Z75741.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127728734,"end":127730858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230105.1","gene_symbol":"AL354793.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56618391,"end":56624458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225512.1","gene_symbol":"CR753845.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32008544,"end":32012073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242209.1","gene_symbol":"AC006445.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13647697,"end":13648400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231243.1","gene_symbol":"AC116038.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38823902,"end":38825302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236625.8","gene_symbol":"C4B","gene_name":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]","synonyms":"C4B3,CH,C4B1,CPAMD3,C4F,CO4","biotype":"protein_coding","ncbi_id":"721","summary":"This gene encodes the basic form of complement factor 4, and together with the C4A gene, is part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, May 2020]","start":31996944,"end":32011233,"strand":1,"description":"complement C4B (Chido blood group) [Source:HGNC Symbol;Acc:HGNC:1324]"}, {"versioned_ensembl_gene_id":"ENSG00000267749.1","gene_symbol":"AC092068.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2641838,"end":2643853,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224548.1","gene_symbol":"Z75741.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127796124,"end":127796733,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227999.1","gene_symbol":"MTND5P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39644]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873206","summary":null,"start":44473723,"end":44475097,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39644]"}, {"versioned_ensembl_gene_id":"ENSG00000176533.12","gene_symbol":"GNG7","gene_name":"G protein subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:4410]","synonyms":"FLJ00058","biotype":"protein_coding","ncbi_id":"2788","summary":null,"start":2511219,"end":2702709,"strand":-1,"description":"G protein subunit gamma 7 [Source:HGNC Symbol;Acc:HGNC:4410]"}, {"versioned_ensembl_gene_id":"ENSG00000273484.1","gene_symbol":"OR6R2P","gene_name":"olfactory receptor family 6 subfamily R member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31307]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403294","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":21797460,"end":21797759,"strand":1,"description":"olfactory receptor family 6 subfamily R member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31307]"}, {"versioned_ensembl_gene_id":"ENSG00000250634.5","gene_symbol":"LINC01182","gene_name":"long intergenic non-protein coding RNA 1182 [Source:HGNC Symbol;Acc:HGNC:49564]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929071","summary":null,"start":13655179,"end":13977075,"strand":1,"description":"long intergenic non-protein coding RNA 1182 [Source:HGNC Symbol;Acc:HGNC:49564]"}, {"versioned_ensembl_gene_id":"ENSG00000138039.14","gene_symbol":"LHCGR","gene_name":"luteinizing hormone/choriogonadotropin receptor [Source:HGNC Symbol;Acc:HGNC:6585]","synonyms":"LHR,LGR2,LCGR,HHG,ULG5","biotype":"protein_coding","ncbi_id":"3973","summary":"This gene encodes the receptor for both luteinizing hormone and choriogonadotropin. This receptor belongs to the G-protein coupled receptor 1 family, and its activity is mediated by G proteins which activate adenylate cyclase. Mutations in this gene result in disorders of male secondary sexual character development, including familial male precocious puberty, also known as testotoxicosis, hypogonadotropic hypogonadism, Leydig cell adenoma with precocious puberty, and male pseudohermaphtoditism with Leydig cell hypoplasia. [provided by RefSeq, Jul 2008]","start":48686775,"end":48755730,"strand":-1,"description":"luteinizing hormone/choriogonadotropin receptor [Source:HGNC Symbol;Acc:HGNC:6585]"}, {"versioned_ensembl_gene_id":"ENSG00000274225.1","gene_symbol":"AP001065.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44477850,"end":44478493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261497.1","gene_symbol":"AC091304.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28362796,"end":28365731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228709.1","gene_symbol":"AP001065.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44485577,"end":44490288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250497.1","gene_symbol":"AC007126.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13777377,"end":13782157,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162699.5","gene_symbol":"DNAJA1P5","gene_name":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39341]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"94236","summary":null,"start":101893105,"end":101894047,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:39341]"}, {"versioned_ensembl_gene_id":"ENSG00000277352.1","gene_symbol":"AP001065.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44494874,"end":44495519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272076.1","gene_symbol":"AC090186.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51810110,"end":51810681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123165.8","gene_symbol":"ACTRT1","gene_name":"actin related protein T1 [Source:HGNC Symbol;Acc:HGNC:24027]","synonyms":"KIAA0705,Arp-T1,ARIP1,AIP1","biotype":"protein_coding","ncbi_id":"139741","summary":"This gene encodes a protein related to the cytoskeletal protein beta-actin. This protein is a major component of the calyx in the perinuclear theca of mammalian sperm heads, and it therefore likely functions in spermatid formation. This gene is intronless and is similar to a related gene located on chromosome 1. A related pseudogene has also been identified approximately 75 kb downstream of this gene on chromosome X. [provided by RefSeq, May 2010]","start":128050962,"end":128052398,"strand":-1,"description":"actin related protein T1 [Source:HGNC Symbol;Acc:HGNC:24027]"}, {"versioned_ensembl_gene_id":"ENSG00000118733.16","gene_symbol":"OLFM3","gene_name":"olfactomedin 3 [Source:HGNC Symbol;Acc:HGNC:17990]","synonyms":"NOE3","biotype":"protein_coding","ncbi_id":"118427","summary":null,"start":101802574,"end":101997030,"strand":-1,"description":"olfactomedin 3 [Source:HGNC Symbol;Acc:HGNC:17990]"}, {"versioned_ensembl_gene_id":"ENSG00000237334.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32935645,"end":32935719,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000260084.1","gene_symbol":"AC126773.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68573782,"end":68589512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276076.4","gene_symbol":"FP236240.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":6560714,"end":6564489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134440.11","gene_symbol":"NARS","gene_name":"asparaginyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:7643]","synonyms":"NARS1","biotype":"protein_coding","ncbi_id":"4677","summary":" Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. Asparaginyl-tRNA synthetase is localized to the cytoplasm and belongs to the class II family of tRNA synthetases. The N-terminal domain represents the signature sequence for the eukaryotic asparaginyl-tRNA synthetases. [provided by RefSeq, Jul 2008]","start":57600656,"end":57622213,"strand":-1,"description":"asparaginyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:7643]"}, {"versioned_ensembl_gene_id":"ENSG00000184939.15","gene_symbol":"ZFP90","gene_name":"ZFP90 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23329]","synonyms":"ZNF756,NK10,KIAA1954","biotype":"protein_coding","ncbi_id":"146198","summary":"This gene encodes a member of the zinc finger protein family that modulates gene expression. The encoded protein derepresses the transcription of certain fetal cardiac genes and may contribute to the genetic reprogramming that occurs during the development of heart failure. Genome wide association studies have identified this gene among ulcerative colitis risk loci. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":68530090,"end":68576072,"strand":1,"description":"ZFP90 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:23329]"}, {"versioned_ensembl_gene_id":"ENSG00000251424.1","gene_symbol":"AC021146.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68834213,"end":68834368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279365.1","gene_symbol":"AP000695.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36485867,"end":36487760,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267214.1","gene_symbol":"AC092068.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2631954,"end":2632849,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234513.1","gene_symbol":"AC073072.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22773646,"end":22773993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223741.1","gene_symbol":"PSMD4P1","gene_name":"proteasome 26S subunit, non-ATPase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9562]","synonyms":"PSMD4P,PSMD15","biotype":"processed_pseudogene","ncbi_id":"54035","summary":null,"start":36485983,"end":36487411,"strand":-1,"description":"proteasome 26S subunit, non-ATPase 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9562]"}, {"versioned_ensembl_gene_id":"ENSG00000276097.1","gene_symbol":"AC006538.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2700689,"end":2701266,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257237.1","gene_symbol":"AC018448.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":39058028,"end":39059933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276231.4","gene_symbol":"PIK3R6","gene_name":"phosphoinositide-3-kinase regulatory subunit 6 [Source:HGNC Symbol;Acc:HGNC:27101]","synonyms":"p87PIKAP,HsT41028,FLJ34500,C17orf38","biotype":"protein_coding","ncbi_id":"146850","summary":"Phosphoinositide 3-kinase gamma is a lipid kinase that produces the lipid second messenger phosphatidylinositol 3,4,5-trisphosphate. The kinase is composed of a catalytic subunit and one of several regulatory subunits, and is chiefly activated by G protein-coupled receptors. This gene encodes a regulatory subunit, and is distantly related to the phosphoinositide-3-kinase, regulatory subunit 5 gene which is located adjacent to this gene on chromosome 7. The orthologous protein in the mouse binds to both the catalytic subunit and to G(beta/gamma), and mediates activation of the kinase subunit downstream of G protein-coupled receptors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":8802723,"end":8867677,"strand":-1,"description":"phosphoinositide-3-kinase regulatory subunit 6 [Source:HGNC Symbol;Acc:HGNC:27101]"}, {"versioned_ensembl_gene_id":"ENSG00000105694.3","gene_symbol":"ELOCP28","gene_name":"elongin C pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49169]","synonyms":"TCEB1P28","biotype":"processed_pseudogene","ncbi_id":"100287483","summary":null,"start":2538112,"end":2538754,"strand":1,"description":"elongin C pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49169]"}, {"versioned_ensembl_gene_id":"ENSG00000188452.13","gene_symbol":"CERKL","gene_name":"ceramide kinase like [Source:HGNC Symbol;Acc:HGNC:21699]","synonyms":"RP26","biotype":"protein_coding","ncbi_id":"375298","summary":"This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.[provided by RefSeq, May 2010]","start":181536676,"end":181680665,"strand":-1,"description":"ceramide kinase like [Source:HGNC Symbol;Acc:HGNC:21699]"}, {"versioned_ensembl_gene_id":"ENSG00000233818.1","gene_symbol":"AP000695.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36445731,"end":36532408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147050.14","gene_symbol":"KDM6A","gene_name":"lysine demethylase 6A [Source:HGNC Symbol;Acc:HGNC:12637]","synonyms":"UTX","biotype":"protein_coding","ncbi_id":"7403","summary":"This gene is located on the X chromosome and is the corresponding locus to a Y-linked gene which encodes a tetratricopeptide repeat (TPR) protein. The encoded protein of this gene contains a JmjC-domain and catalyzes the demethylation of tri/dimethylated histone H3. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2014]","start":44873177,"end":45112602,"strand":1,"description":"lysine demethylase 6A [Source:HGNC Symbol;Acc:HGNC:12637]"}, {"versioned_ensembl_gene_id":"ENSG00000258144.1","gene_symbol":"LINC02406","gene_name":"long intergenic non-protein coding RNA 2406 [Source:HGNC Symbol;Acc:HGNC:53334]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369730","summary":null,"start":39087713,"end":39092874,"strand":-1,"description":"long intergenic non-protein coding RNA 2406 [Source:HGNC Symbol;Acc:HGNC:53334]"}, {"versioned_ensembl_gene_id":"ENSG00000230479.1","gene_symbol":"AP000695.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36430360,"end":36481070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149761.8","gene_symbol":"NUDT22","gene_name":"nudix hydrolase 22 [Source:HGNC Symbol;Acc:HGNC:28189]","synonyms":"MGC13045","biotype":"protein_coding","ncbi_id":"84304","summary":null,"start":64225941,"end":64230686,"strand":1,"description":"nudix hydrolase 22 [Source:HGNC Symbol;Acc:HGNC:28189]"}, {"versioned_ensembl_gene_id":"ENSG00000270718.1","gene_symbol":"AC084373.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39170646,"end":39170880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238108.1","gene_symbol":"AL139135.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190797524,"end":190797956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271443.1","gene_symbol":"AC011247.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":38535258,"end":38536249,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254315.1","gene_symbol":"AC023632.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94533628,"end":94534391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231175.1","gene_symbol":"LINC01720","gene_name":"long intergenic non-protein coding RNA 1720 [Source:HGNC Symbol;Acc:HGNC:52507]","synonyms":null,"biotype":"lincRNA","ncbi_id":"440704","summary":null,"start":190624890,"end":190801658,"strand":1,"description":"long intergenic non-protein coding RNA 1720 [Source:HGNC Symbol;Acc:HGNC:52507]"}, {"versioned_ensembl_gene_id":"ENSG00000236025.1","gene_symbol":"AL139135.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190781787,"end":190781995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164944.11","gene_symbol":"VIRMA","gene_name":"vir like m6A methyltransferase associated [Source:HGNC Symbol;Acc:HGNC:24500]","synonyms":"KIAA1429,fSAP121,DKFZP434I116","biotype":"protein_coding","ncbi_id":"25962","summary":null,"start":94487693,"end":94553529,"strand":-1,"description":"vir like m6A methyltransferase associated [Source:HGNC Symbol;Acc:HGNC:24500]"}, {"versioned_ensembl_gene_id":"ENSG00000120498.13","gene_symbol":"TEX11","gene_name":"testis expressed 11 [Source:HGNC Symbol;Acc:HGNC:11733]","synonyms":"TGC1,TSGA3","biotype":"protein_coding","ncbi_id":"56159","summary":"This gene is X-linked and is expressed in only male germ cells. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":70528940,"end":70908731,"strand":-1,"description":"testis expressed 11 [Source:HGNC Symbol;Acc:HGNC:11733]"}, {"versioned_ensembl_gene_id":"ENSG00000234661.2","gene_symbol":"CHL1-AS1","gene_name":"CHL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40148]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927193","summary":null,"start":363370,"end":385795,"strand":-1,"description":"CHL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40148]"}, {"versioned_ensembl_gene_id":"ENSG00000228803.1","gene_symbol":"MTCYBP42","gene_name":"mitochondrially encoded cytochrome b pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52310]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729153","summary":null,"start":22747675,"end":22748804,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:52310]"}, {"versioned_ensembl_gene_id":"ENSG00000224318.5","gene_symbol":"CHL1-AS2","gene_name":"CHL1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40147]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"101927174","summary":null,"start":195758,"end":197341,"strand":-1,"description":"CHL1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40147]"}, {"versioned_ensembl_gene_id":"ENSG00000270209.1","gene_symbol":"AL035411.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58552913,"end":58553333,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228020.2","gene_symbol":"HNRNPA1P46","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:48776]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421399","summary":null,"start":191146025,"end":191146961,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:48776]"}, {"versioned_ensembl_gene_id":"ENSG00000261642.1","gene_symbol":"AL713866.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191151510,"end":191154634,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101448.13","gene_symbol":"EPPIN","gene_name":"epididymal peptidase inhibitor [Source:HGNC Symbol;Acc:HGNC:15932]","synonyms":"WFDC7,WAP7,SPINLW1,EPPIN3,EPPIN2,EPPIN1,dJ461P17.2,CT71","biotype":"protein_coding","ncbi_id":"57119","summary":"This gene encodes an epididymal protease inhibitor, which contains both kunitz-type and WAP-type four-disulfide core (WFDC) protease inhibitor consensus sequences. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene is a member of the WFDC gene family and belongs to the telomeric cluster. The protein can inhibit human sperm motility and exhibits antimicrobial activity against E. coli, and polymorphisms in this gene are associated with male infertility. Read-through transcription also exists between this gene and the downstream WFDC6 (WAP four-disulfide core domain 6) gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]","start":45540626,"end":45547752,"strand":-1,"description":"epididymal peptidase inhibitor [Source:HGNC Symbol;Acc:HGNC:15932]"}, {"versioned_ensembl_gene_id":"ENSG00000282498.1","gene_symbol":"AC015849.12","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":35868967,"end":35885863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198284.9","gene_symbol":"NUP210P1","gene_name":"nucleoporin 210 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27399]","synonyms":"C3orf46","biotype":"transcribed_processed_pseudogene","ncbi_id":"255330","summary":null,"start":126660609,"end":126671939,"strand":1,"description":"nucleoporin 210 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:27399]"}, {"versioned_ensembl_gene_id":"ENSG00000270120.1","gene_symbol":"AC007728.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50712844,"end":50713589,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261644.2","gene_symbol":"AC007728.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50727417,"end":50742815,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274233.4","gene_symbol":"CCL5","gene_name":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]","synonyms":"TCP228,SISd,SCYA5,RANTES,MGC17164,D17S136E","biotype":"protein_coding","ncbi_id":"6352","summary":"This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, functions as a chemoattractant for blood monocytes, memory T helper cells and eosinophils. It causes the release of histamine from basophils and activates eosinophils. This cytokine is one of the major HIV-suppressive factors produced by CD8+ cells. It functions as one of the natural ligands for the chemokine receptor chemokine (C-C motif) receptor 5 (CCR5), and it suppresses in vitro replication of the R5 strains of HIV-1, which use CCR5 as a coreceptor. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]","start":35871491,"end":35880793,"strand":-1,"description":"C-C motif chemokine ligand 5 [Source:HGNC Symbol;Acc:HGNC:10632]"}, {"versioned_ensembl_gene_id":"ENSG00000184530.8","gene_symbol":"C6orf58","gene_name":"chromosome 6 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:20960]","synonyms":"LEG1","biotype":"protein_coding","ncbi_id":"352999","summary":null,"start":127519455,"end":127591817,"strand":1,"description":"chromosome 6 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:20960]"}, {"versioned_ensembl_gene_id":"ENSG00000075223.13","gene_symbol":"SEMA3C","gene_name":"semaphorin 3C [Source:HGNC Symbol;Acc:HGNC:10725]","synonyms":"SemE,SEMAE","biotype":"protein_coding","ncbi_id":"10512","summary":"This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017]","start":80742538,"end":80922359,"strand":-1,"description":"semaphorin 3C [Source:HGNC Symbol;Acc:HGNC:10725]"}, {"versioned_ensembl_gene_id":"ENSG00000229998.8","gene_symbol":"PPP1R18","gene_name":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]","synonyms":"KIAA1949,phostensin","biotype":"protein_coding","ncbi_id":"170954","summary":"Protein phosphatase-1 (PP1; see MIM 176875) interacts with regulatory subunits that target the enzyme to different cellular locations and change its activity toward specific substrates. Phostensin is a regulatory subunit that targets PP1 to F-actin (see MIM 102610) cytoskeleton (Kao et al., 2007 [PubMed 17374523]).[supplied by OMIM, Mar 2008]","start":30721049,"end":30732555,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 18 [Source:HGNC Symbol;Acc:HGNC:29413]"}, {"versioned_ensembl_gene_id":"ENSG00000167207.12","gene_symbol":"NOD2","gene_name":"nucleotide binding oligomerization domain containing 2 [Source:HGNC Symbol;Acc:HGNC:5331]","synonyms":"IBD1,CLR16.3,CD,CARD15,BLAU,PSORAS1,NLRC2","biotype":"protein_coding","ncbi_id":"64127","summary":"This gene is a member of the Nod1/Apaf-1 family and encodes a protein with two caspase recruitment (CARD) domains and six leucine-rich repeats (LRRs). The protein is primarily expressed in the peripheral blood leukocytes. It plays a role in the immune response to intracellular bacterial lipopolysaccharides (LPS) by recognizing the muramyl dipeptide (MDP) derived from them and activating the NFKB protein. Mutations in this gene have been associated with Crohn disease and Blau syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":50693603,"end":50734041,"strand":1,"description":"nucleotide binding oligomerization domain containing 2 [Source:HGNC Symbol;Acc:HGNC:5331]"}, {"versioned_ensembl_gene_id":"ENSG00000280145.3","gene_symbol":"CU638689.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6630182,"end":6670695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134121.9","gene_symbol":"CHL1","gene_name":"cell adhesion molecule L1 like [Source:HGNC Symbol;Acc:HGNC:1939]","synonyms":"MGC132578,L1CAM2,FLJ44930,CALL","biotype":"protein_coding","ncbi_id":"10752","summary":"The protein encoded by this gene is a member of the L1 gene family of neural cell adhesion molecules. It is a neural recognition molecule that may be involved in signal transduction pathways. The deletion of one copy of this gene may be responsible for mental defects in patients with 3p- syndrome. This protein may also play a role in the growth of certain cancers. Alternate splicing results in both coding and non-coding variants. [provided by RefSeq, Nov 2011]","start":196596,"end":409417,"strand":1,"description":"cell adhesion molecule L1 like [Source:HGNC Symbol;Acc:HGNC:1939]"}, {"versioned_ensembl_gene_id":"ENSG00000233963.2","gene_symbol":"ATP8A2P3","gene_name":"ATPase phospholipid transporting 8A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42641]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874518","summary":null,"start":26094724,"end":26154175,"strand":-1,"description":"ATPase phospholipid transporting 8A2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42641]"}, {"versioned_ensembl_gene_id":"ENSG00000211747.3","gene_symbol":"TRBV20-1","gene_name":"T-cell receptor beta variable 20-1 [Source:HGNC Symbol;Acc:HGNC:12196]","synonyms":"TRBV201,TCRBV2S1,TCRBV20S1","biotype":"TR_V_gene","ncbi_id":"28567","summary":null,"start":142626649,"end":142627399,"strand":1,"description":"T-cell receptor beta variable 20-1 [Source:HGNC Symbol;Acc:HGNC:12196]"}, {"versioned_ensembl_gene_id":"ENSG00000234706.1","gene_symbol":"PRUNEP1","gene_name":"prune exopolyphosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39723]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129595","summary":null,"start":26117548,"end":26118964,"strand":-1,"description":"prune exopolyphosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39723]"}, {"versioned_ensembl_gene_id":"ENSG00000251578.1","gene_symbol":"TRBV21-1","gene_name":"T-cell receptor beta variable 21-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12198]","synonyms":"TCRBV21S1,TCRBV10S1P,TRBV211","biotype":"TR_V_pseudogene","ncbi_id":"28566","summary":null,"start":142636924,"end":142637384,"strand":1,"description":"T-cell receptor beta variable 21-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12198]"}, {"versioned_ensembl_gene_id":"ENSG00000240578.1","gene_symbol":"TRBV22-1","gene_name":"T-cell receptor beta variable 22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12200]","synonyms":"TRBV22,TCRBV29S1P,TCRBV22S1","biotype":"TR_V_pseudogene","ncbi_id":"28565","summary":null,"start":142641746,"end":142642196,"strand":1,"description":"T-cell receptor beta variable 22-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12200]"}, {"versioned_ensembl_gene_id":"ENSG00000260398.1","gene_symbol":"AC068700.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":78605952,"end":78609705,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284240.1","gene_symbol":"AC099062.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":87212669,"end":87264741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278878.1","gene_symbol":"CU638689.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6667304,"end":6670667,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211749.1","gene_symbol":"TRBV23-1","gene_name":"T-cell receptor beta variable 23-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12201]","synonyms":"TRBV231,TCRBV23S1,TCRBV19S1P","biotype":"TR_V_gene","ncbi_id":"28564","summary":null,"start":142645961,"end":142646467,"strand":1,"description":"T-cell receptor beta variable 23-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:12201]"}, {"versioned_ensembl_gene_id":"ENSG00000271187.1","gene_symbol":"AL713866.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":191179521,"end":191179739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196091.13","gene_symbol":"MYBPC1","gene_name":"myosin binding protein C, slow type [Source:HGNC Symbol;Acc:HGNC:7549]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4604","summary":"This gene encodes a member of the myosin-binding protein C family. Myosin-binding protein C family members are myosin-associated proteins found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The encoded protein is the slow skeletal muscle isoform of myosin-binding protein C and plays an important role in muscle contraction by recruiting muscle-type creatine kinase to myosin filaments. Mutations in this gene are associated with distal arthrogryposis type I. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":101568353,"end":101686018,"strand":1,"description":"myosin binding protein C, slow type [Source:HGNC Symbol;Acc:HGNC:7549]"}, {"versioned_ensembl_gene_id":"ENSG00000211750.2","gene_symbol":"TRBV24-1","gene_name":"T-cell receptor beta variable 24-1 [Source:HGNC Symbol;Acc:HGNC:12203]","synonyms":"TRBV241,TCRBV24S1,TCRBV15S1","biotype":"TR_V_gene","ncbi_id":"28563","summary":null,"start":142656701,"end":142657213,"strand":1,"description":"T-cell receptor beta variable 24-1 [Source:HGNC Symbol;Acc:HGNC:12203]"}, {"versioned_ensembl_gene_id":"ENSG00000224862.1","gene_symbol":"CR942271.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30918008,"end":30926645,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204568.11","gene_symbol":"MRPS18B","gene_name":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]","synonyms":"C6orf14,MRPS18-2,HSPC183,PTD017","biotype":"protein_coding","ncbi_id":"28973","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Jul 2008]","start":30617709,"end":30626395,"strand":1,"description":"mitochondrial ribosomal protein S18B [Source:HGNC Symbol;Acc:HGNC:14516]"}, {"versioned_ensembl_gene_id":"ENSG00000270672.1","gene_symbol":"MTRNR2L6","gene_name":"MT-RNR2-like 6 [Source:HGNC Symbol;Acc:HGNC:37163]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100463482","summary":null,"start":142666272,"end":142667718,"strand":1,"description":"MT-RNR2-like 6 [Source:HGNC Symbol;Acc:HGNC:37163]"}, {"versioned_ensembl_gene_id":"ENSG00000104518.10","gene_symbol":"GSDMD","gene_name":"gasdermin D [Source:HGNC Symbol;Acc:HGNC:25697]","synonyms":"GSDMDC1,FLJ12150,DF5L","biotype":"protein_coding","ncbi_id":"79792","summary":"Gasdermin D is a member of the gasdermin family. Members of this family appear to play a role in regulation of epithelial proliferation. Gasdermin D has been suggested to act as a tumor suppressor. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009]","start":143553207,"end":143563062,"strand":1,"description":"gasdermin D [Source:HGNC Symbol;Acc:HGNC:25697]"}, {"versioned_ensembl_gene_id":"ENSG00000261471.1","gene_symbol":"AC092145.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84594393,"end":84596826,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229900.1","gene_symbol":"HSPD1P21","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38592]","synonyms":"HSPD1-3P","biotype":"processed_pseudogene","ncbi_id":"100462990","summary":null,"start":45539983,"end":45540227,"strand":-1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38592]"}, {"versioned_ensembl_gene_id":"ENSG00000103187.7","gene_symbol":"COTL1","gene_name":"coactosin like F-actin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:18304]","synonyms":"CLP","biotype":"protein_coding","ncbi_id":"23406","summary":"This gene encodes one of the numerous actin-binding proteins which regulate the actin cytoskeleton. This protein binds F-actin, and also interacts with 5-lipoxygenase, which is the first committed enzyme in leukotriene biosynthesis. Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region, the best alignments for this gene are to chromosome 16. The Smith-Magenis syndrome region is the site of two related pseudogenes. [provided by RefSeq, Jul 2008]","start":84565594,"end":84618077,"strand":-1,"description":"coactosin like F-actin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:18304]"}, {"versioned_ensembl_gene_id":"ENSG00000243543.8","gene_symbol":"WFDC6","gene_name":"WAP four-disulfide core domain 6 [Source:HGNC Symbol;Acc:HGNC:16164]","synonyms":"WAP6,dJ461P17.11,C20orf171","biotype":"protein_coding","ncbi_id":"140870","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Read-through transcription exists between this gene and the upstream SPINLW1 (serine peptidase inhibitor-like, with Kunitz and WAP domains 1) gene. [provided by RefSeq, Nov 2010]","start":45534196,"end":45539495,"strand":-1,"description":"WAP four-disulfide core domain 6 [Source:HGNC Symbol;Acc:HGNC:16164]"}, {"versioned_ensembl_gene_id":"ENSG00000143013.12","gene_symbol":"LMO4","gene_name":"LIM domain only 4 [Source:HGNC Symbol;Acc:HGNC:6644]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8543","summary":"This gene encodes a cysteine-rich protein that contains two LIM domains but lacks a DNA-binding homeodomain. The encoded protein may play a role as a transcriptional regulator or as an oncogene. [provided by RefSeq, Aug 2008]","start":87328468,"end":87348923,"strand":1,"description":"LIM domain only 4 [Source:HGNC Symbol;Acc:HGNC:6644]"}, {"versioned_ensembl_gene_id":"ENSG00000163590.13","gene_symbol":"PPM1L","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1L [Source:HGNC Symbol;Acc:HGNC:16381]","synonyms":"PP2CE","biotype":"protein_coding","ncbi_id":"151742","summary":"The protein encoded by this gene is a magnesium or manganese-requiring phosphatase that is involved in several signaling pathways. The encoded protein downregulates apoptosis signal-regulating kinase 1, a protein that initiates a signaling cascade that leads to apoptosis when cells are subjected to cytotoxic stresses. This protein also is an endoplasmic reticulum transmembrane protein that helps regulate ceramide transport from the endoplasmic reticulum to the Golgi apparatus. Finally, this gene may be involved in adiposity since it is upregulated in adipose tissues. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":160755602,"end":161078907,"strand":1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1L [Source:HGNC Symbol;Acc:HGNC:16381]"}, {"versioned_ensembl_gene_id":"ENSG00000120664.10","gene_symbol":"SPG20-AS1","gene_name":"SPG20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39933]","synonyms":"SPG20OS,C13orf43","biotype":"antisense_RNA","ncbi_id":"100507135","summary":null,"start":36346431,"end":36369601,"strand":1,"description":"SPG20 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39933]"}, {"versioned_ensembl_gene_id":"ENSG00000149781.12","gene_symbol":"FERMT3","gene_name":"fermitin family member 3 [Source:HGNC Symbol;Acc:HGNC:23151]","synonyms":"KIND3,URP2,UNC112C,MIG2B,MIG-2,MGC10966","biotype":"protein_coding","ncbi_id":"83706","summary":"Kindlins are a small family of proteins that mediate protein-protein interactions involved in integrin activation and thereby have a role in cell adhesion, migration, differentiation, and proliferation. The protein encoded by this gene has a key role in the regulation of hemostasis and thrombosis. This protein may also help maintain the membrane skeleton of erythrocytes. Mutations in this gene cause the autosomal recessive leukocyte adhesion deficiency syndrome-III (LAD-III). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2010]","start":64206678,"end":64223886,"strand":1,"description":"fermitin family member 3 [Source:HGNC Symbol;Acc:HGNC:23151]"}, {"versioned_ensembl_gene_id":"ENSG00000153684.14","gene_symbol":"GOLGA8F","gene_name":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]","synonyms":"DKFZp434P162","biotype":"protein_coding","ncbi_id":"100132565","summary":null,"start":28378621,"end":28392018,"strand":1,"description":"golgin A8 family member F [Source:HGNC Symbol;Acc:HGNC:32378]"}, {"versioned_ensembl_gene_id":"ENSG00000240135.1","gene_symbol":"AC114876.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":72876737,"end":72878102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237637.1","gene_symbol":"FRY-AS1","gene_name":"FRY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39725]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507099","summary":null,"start":32025314,"end":32031639,"strand":-1,"description":"FRY antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39725]"}, {"versioned_ensembl_gene_id":"ENSG00000249139.1","gene_symbol":"EPPIN-WFDC6","gene_name":"EPPIN-WFDC6 readthrough [Source:HGNC Symbol;Acc:HGNC:38825]","synonyms":"SPINLW1-WFDC6","biotype":"protein_coding","ncbi_id":"100526773","summary":"This locus represents naturally occurring read-through transcription between the neighboring SPINLW1 (serine peptidase inhibitor-like, with Kunitz and WAP domains 1) and WFDC6 (WAP four-disulfide core domain 6) genes. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]","start":45536986,"end":45547426,"strand":-1,"description":"EPPIN-WFDC6 readthrough [Source:HGNC Symbol;Acc:HGNC:38825]"}, {"versioned_ensembl_gene_id":"ENSG00000233882.2","gene_symbol":"LINC01680","gene_name":"long intergenic non-protein coding RNA 1680 [Source:HGNC Symbol;Acc:HGNC:52467]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371660","summary":null,"start":191221159,"end":191228467,"strand":-1,"description":"long intergenic non-protein coding RNA 1680 [Source:HGNC Symbol;Acc:HGNC:52467]"}, {"versioned_ensembl_gene_id":"ENSG00000271277.1","gene_symbol":"AL356280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101882516,"end":101882894,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184292.6","gene_symbol":"TACSTD2","gene_name":"tumor associated calcium signal transducer 2 [Source:HGNC Symbol;Acc:HGNC:11530]","synonyms":"TROP2,M1S1,GA733-1,EGP-1","biotype":"protein_coding","ncbi_id":"4070","summary":"This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy.[provided by RefSeq, Dec 2009]","start":58575423,"end":58577773,"strand":-1,"description":"tumor associated calcium signal transducer 2 [Source:HGNC Symbol;Acc:HGNC:11530]"}, {"versioned_ensembl_gene_id":"ENSG00000223344.1","gene_symbol":"AL359081.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191858707,"end":191890229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249505.1","gene_symbol":"AC108673.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129045763,"end":129046921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228215.2","gene_symbol":"AL954650.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":191875495,"end":192011260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260616.6","gene_symbol":"AC007728.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50783859,"end":50803338,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259878.1","gene_symbol":"AC126323.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62230384,"end":62231895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261648.1","gene_symbol":"AC106730.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31546698,"end":31547237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166104.14","gene_symbol":"AC126323.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62227896,"end":62253235,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232135.1","gene_symbol":"AL031663.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45536796,"end":45537014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169704.4","gene_symbol":"GP9","gene_name":"glycoprotein IX platelet [Source:HGNC Symbol;Acc:HGNC:4444]","synonyms":"GPIX,CD42a","biotype":"protein_coding","ncbi_id":"2815","summary":"This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency. [provided by RefSeq, Oct 2008]","start":129060767,"end":129062406,"strand":1,"description":"glycoprotein IX platelet [Source:HGNC Symbol;Acc:HGNC:4444]"}, {"versioned_ensembl_gene_id":"ENSG00000213547.3","gene_symbol":"VN1R64P","gene_name":"vomeronasal 1 receptor 64 pseudogene [Source:HGNC Symbol;Acc:HGNC:37384]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"730196","summary":null,"start":31546805,"end":31547737,"strand":1,"description":"vomeronasal 1 receptor 64 pseudogene [Source:HGNC Symbol;Acc:HGNC:37384]"}, {"versioned_ensembl_gene_id":"ENSG00000271266.1","gene_symbol":"LAPTM4BP2","gene_name":"lysosomal protein transmembrane 4 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51935]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075219","summary":null,"start":72884234,"end":72884679,"strand":1,"description":"lysosomal protein transmembrane 4 beta pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51935]"}, {"versioned_ensembl_gene_id":"ENSG00000253907.1","gene_symbol":"AC021678.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28238430,"end":28238905,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261475.2","gene_symbol":"LINC02190","gene_name":"long intergenic non-protein coding RNA 2190 [Source:HGNC Symbol;Acc:HGNC:53052]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371173","summary":null,"start":31549143,"end":31553567,"strand":-1,"description":"long intergenic non-protein coding RNA 2190 [Source:HGNC Symbol;Acc:HGNC:53052]"}, {"versioned_ensembl_gene_id":"ENSG00000103932.11","gene_symbol":"RPAP1","gene_name":"RNA polymerase II associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24567]","synonyms":"MGC858,KIAA1403,FLJ12732,DKFZP727M111","biotype":"protein_coding","ncbi_id":"26015","summary":"This protein forms part of the RNA polymerase II (RNAPII) enzyme complex and may recruit RNAPII to chromatin through its interaction with acetylated histones. [provided by RefSeq, Jul 2012]","start":41517176,"end":41544269,"strand":-1,"description":"RNA polymerase II associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24567]"}, {"versioned_ensembl_gene_id":"ENSG00000243244.5","gene_symbol":"STON1","gene_name":"stonin 1 [Source:HGNC Symbol;Acc:HGNC:17003]","synonyms":"stoned-b1,SBLF","biotype":"protein_coding","ncbi_id":"11037","summary":"Endocytosis of cell surface proteins is mediated by a complex molecular machinery that assembles on the inner surface of the plasma membrane. This gene encodes one of two human homologs of the Drosophila melanogaster stoned B protein. This protein is related to components of the endocytic machinery and exhibits a modular structure consisting of an N-terminal proline-rich domain, a central region of homology specific to the human stoned B-like proteins, and a C-terminal region homologous to the mu subunits of adaptor protein (AP) complexes. Read-through transcription of this gene into the neighboring downstream gene, which encodes TFIIA-alpha/beta-like factor, generates a transcript (SALF), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]","start":48529383,"end":48598513,"strand":1,"description":"stonin 1 [Source:HGNC Symbol;Acc:HGNC:17003]"}, {"versioned_ensembl_gene_id":"ENSG00000236642.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29849350,"end":29849494,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000238004.1","gene_symbol":"AC009227.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154459857,"end":154460820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260883.1","gene_symbol":"VN1R65P","gene_name":"vomeronasal 1 receptor 65 pseudogene [Source:HGNC Symbol;Acc:HGNC:37385]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100128384","summary":null,"start":31554105,"end":31554912,"strand":1,"description":"vomeronasal 1 receptor 65 pseudogene [Source:HGNC Symbol;Acc:HGNC:37385]"}, {"versioned_ensembl_gene_id":"ENSG00000282499.1","gene_symbol":"TRBV25-1","gene_name":"T-cell receptor beta variable 25-1 [Source:HGNC Symbol;Acc:HGNC:12205]","synonyms":"TRBV251,TCRBV25S1,TCRBV11S1A1T","biotype":"TR_V_gene","ncbi_id":"28562","summary":null,"start":142670740,"end":142671244,"strand":1,"description":"T-cell receptor beta variable 25-1 [Source:HGNC Symbol;Acc:HGNC:12205]"}, {"versioned_ensembl_gene_id":"ENSG00000083799.17","gene_symbol":"CYLD","gene_name":"CYLD lysine 63 deubiquitinase [Source:HGNC Symbol;Acc:HGNC:2584]","synonyms":"USPL2,KIAA0849,CYLD1","biotype":"protein_coding","ncbi_id":"1540","summary":"This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":50742050,"end":50801935,"strand":1,"description":"CYLD lysine 63 deubiquitinase [Source:HGNC Symbol;Acc:HGNC:2584]"}, {"versioned_ensembl_gene_id":"ENSG00000235949.1","gene_symbol":"AC061961.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154696462,"end":154697817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225069.3","gene_symbol":"AL080312.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25099105,"end":25099928,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223537.2","gene_symbol":"AL109947.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109487906,"end":109506800,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156103.15","gene_symbol":"MMP16","gene_name":"matrix metallopeptidase 16 [Source:HGNC Symbol;Acc:HGNC:7162]","synonyms":"MT3-MMP,DKFZp761D112,C8orf57","biotype":"protein_coding","ncbi_id":"4325","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The encoded protein activates MMP2 by cleavage. This gene was once referred to as MT-MMP2, but was renamed as MT-MMP3 or MMP16. [provided by RefSeq, Oct 2010]","start":88032009,"end":88328025,"strand":-1,"description":"matrix metallopeptidase 16 [Source:HGNC Symbol;Acc:HGNC:7162]"}, {"versioned_ensembl_gene_id":"ENSG00000204569.9","gene_symbol":"PPP1R10","gene_name":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]","synonyms":"CAT53,p99,FB19,PNUTS","biotype":"protein_coding","ncbi_id":"5514","summary":"This gene encodes a protein phosphatase 1 binding protein. The encoded protein plays a role in many cellular processes including cell cycle progression, DNA repair and apoptosis by regulating the activity of protein phosphatase 1. This gene lies within the major histocompatibility complex class I region on chromosome 6, and alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]","start":30600400,"end":30618612,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 10 [Source:HGNC Symbol;Acc:HGNC:9284]"}, {"versioned_ensembl_gene_id":"ENSG00000235673.1","gene_symbol":"AL929472.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37840986,"end":37841676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237218.3","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29879053,"end":29881769,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000239992.1","gene_symbol":"TRBVA","gene_name":"T-cell receptor beta variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12247]","synonyms":"TCRBV33S1","biotype":"TR_V_pseudogene","ncbi_id":"28556","summary":null,"start":142681415,"end":142681869,"strand":1,"description":"T-cell receptor beta variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12247]"}, {"versioned_ensembl_gene_id":"ENSG00000155085.15","gene_symbol":"AK9","gene_name":"adenylate kinase 9 [Source:HGNC Symbol;Acc:HGNC:33814]","synonyms":"MGC26954,FLJ42177,FLJ25791,dJ70A9.1,C6orf224,C6orf199,AKD2,AKD1","biotype":"protein_coding","ncbi_id":"221264","summary":"The protein encoded by this gene catalyzes the interconversion of nucleosides, possessing both nucleoside monophosphate and diphosphate kinase activities. The encoded protein uses these interconversions to maintain nucleoside homeostasis. [provided by RefSeq, Jul 2016]","start":109492856,"end":109691217,"strand":-1,"description":"adenylate kinase 9 [Source:HGNC Symbol;Acc:HGNC:33814]"}, {"versioned_ensembl_gene_id":"ENSG00000162989.4","gene_symbol":"KCNJ3","gene_name":"potassium voltage-gated channel subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:6264]","synonyms":"Kir3.1,KGA,GIRK1","biotype":"protein_coding","ncbi_id":"3760","summary":"Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and plays an important role in regulating heartbeat. It associates with three other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex that also couples to neurotransmitter receptors in the brain and whereby channel activation can inhibit action potential firing by hyperpolarizing the plasma membrane. These multimeric G-protein-gated inwardly-rectifying potassium (GIRK) channels may play a role in the pathophysiology of epilepsy, addiction, Down's syndrome, ataxia, and Parkinson's disease. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, May 2012]","start":154698299,"end":154858352,"strand":1,"description":"potassium voltage-gated channel subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:6264]"}, {"versioned_ensembl_gene_id":"ENSG00000136710.9","gene_symbol":"CCDC115","gene_name":"coiled-coil domain containing 115 [Source:HGNC Symbol;Acc:HGNC:28178]","synonyms":"MGC12981,FLJ30131,ccp1","biotype":"protein_coding","ncbi_id":"84317","summary":"The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans. [provided by RefSeq, Mar 2016]","start":130338241,"end":130342349,"strand":-1,"description":"coiled-coil domain containing 115 [Source:HGNC Symbol;Acc:HGNC:28178]"}, {"versioned_ensembl_gene_id":"ENSG00000226736.1","gene_symbol":"BX284699.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878595,"end":29879557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249912.1","gene_symbol":"TRBV26","gene_name":"T-cell receptor beta variable 26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12207]","synonyms":"TCRBV28S1P,TCRBV26S1","biotype":"TR_V_pseudogene","ncbi_id":"28561","summary":null,"start":142695699,"end":142696183,"strand":1,"description":"T-cell receptor beta variable 26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12207]"}, {"versioned_ensembl_gene_id":"ENSG00000144035.3","gene_symbol":"NAT8","gene_name":"N-acetyltransferase 8 (putative) [Source:HGNC Symbol;Acc:HGNC:18069]","synonyms":"TSC501,Hcml1,GLA,ATase2","biotype":"protein_coding","ncbi_id":"9027","summary":"This gene, isolated using the differential display method to detect tissue-specific genes, is specifically expressed in kidney and liver. The encoded protein shows amino acid sequence similarity to N-acetyltransferases. A similar protein in Xenopus affects cell adhesion and gastrulation movements, and may be localized in the secretory pathway. A highly similar paralog is found in a cluster with this gene. [provided by RefSeq, Sep 2008]","start":73640832,"end":73642393,"strand":-1,"description":"N-acetyltransferase 8 (putative) [Source:HGNC Symbol;Acc:HGNC:18069]"}, {"versioned_ensembl_gene_id":"ENSG00000281094.1","gene_symbol":"AC233280.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195655565,"end":195657927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278885.1","gene_symbol":"AC106730.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31566360,"end":31567000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230725.5","gene_symbol":"AL035252.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25140789,"end":25149258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261741.5","gene_symbol":"FRG2KP","gene_name":"FSHD region gene 2 family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:51797]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"102724018","summary":null,"start":31563082,"end":31567716,"strand":-1,"description":"FSHD region gene 2 family member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:51797]"}, {"versioned_ensembl_gene_id":"ENSG00000196369.11","gene_symbol":"SRGAP2B","gene_name":"SLIT-ROBO Rho GTPase activating protein 2B [Source:HGNC Symbol;Acc:HGNC:35237]","synonyms":"SRGAP2P2","biotype":"protein_coding","ncbi_id":"647135","summary":"This locus encodes a member of the SLIT-ROBO Rho GTPase activating protein family. This human-specific locus resulted from incomplete segmental duplication of the SLIT-ROBO Rho GTPase activating protein 2 locus. The encoded protein lacks the GTPase activating protein domain compared to proteins encoded by SLIT-ROBO Rho GTPase activating protein 2. The functionality of the protein encoded by this locus has been questioned, as several normal individuals with homozygous deletions for this locus have been identified, and the expression of this locus appears to be much lower than the similar SLIT-ROBO Rho GTPase activating protein 2C (SRGAP2C) locus. The SRGAP2C locus has been shown to encode a protein that functions antagonistically to SLIT-ROBO Rho GTPase activating protein 2 in cortical neuron development. [provided by RefSeq, Dec 2012]","start":144887265,"end":145095528,"strand":-1,"description":"SLIT-ROBO Rho GTPase activating protein 2B [Source:HGNC Symbol;Acc:HGNC:35237]"}, {"versioned_ensembl_gene_id":"ENSG00000264666.1","gene_symbol":"AC020558.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17591428,"end":17610485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133027.17","gene_symbol":"PEMT","gene_name":"phosphatidylethanolamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8830]","synonyms":"PEMT2,PEMPT","biotype":"protein_coding","ncbi_id":"10400","summary":"Phosphatidylcholine (PC) is the most abundant mammalian phospholipid. This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. Another distinct synthetic pathway in nucleated cells converts intracellular choline to phosphatidylcholine by a three-step process. The protein isoforms encoded by this gene localize to the endoplasmic reticulum and mitochondria-associated membranes. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012]","start":17505563,"end":17591708,"strand":-1,"description":"phosphatidylethanolamine N-methyltransferase [Source:HGNC Symbol;Acc:HGNC:8830]"}, {"versioned_ensembl_gene_id":"ENSG00000260062.3","gene_symbol":"GOLGA2P11","gene_name":"golgin A2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:26788]","synonyms":"FLJ38723","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"255180","summary":null,"start":62253730,"end":62270680,"strand":-1,"description":"golgin A2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:26788]"}, {"versioned_ensembl_gene_id":"ENSG00000196683.10","gene_symbol":"TOMM7","gene_name":"translocase of outer mitochondrial membrane 7 [Source:HGNC Symbol;Acc:HGNC:21648]","synonyms":"Tom7","biotype":"protein_coding","ncbi_id":"54543","summary":"This gene encodes a subunit of the translocase of the outer mitochondrial membrane. The encoded protein regulates the assembly and stability of the translocase complex. [provided by RefSeq, Oct 2012]","start":22812628,"end":22822852,"strand":-1,"description":"translocase of outer mitochondrial membrane 7 [Source:HGNC Symbol;Acc:HGNC:21648]"}, {"versioned_ensembl_gene_id":"ENSG00000260375.1","gene_symbol":"AC126323.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":62255686,"end":62256421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241911.1","gene_symbol":"TRBVB","gene_name":"T-cell receptor beta variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12248]","synonyms":"TCRBV34S1","biotype":"TR_V_pseudogene","ncbi_id":"28555","summary":null,"start":142711384,"end":142711924,"strand":1,"description":"T-cell receptor beta variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12248]"}, {"versioned_ensembl_gene_id":"ENSG00000188786.9","gene_symbol":"MTF1","gene_name":"metal regulatory transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7428]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4520","summary":"This gene encodes a transcription factor that induces expression of metallothioneins and other genes involved in metal homeostasis in response to heavy metals such as cadmium, zinc, copper, and silver. The protein is a nucleocytoplasmic shuttling protein that accumulates in the nucleus upon heavy metal exposure and binds to promoters containing a metal-responsive element (MRE). [provided by RefSeq, Jul 2008]","start":37809567,"end":37859620,"strand":-1,"description":"metal regulatory transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:7428]"}, {"versioned_ensembl_gene_id":"ENSG00000235720.1","gene_symbol":"GABPAP","gene_name":"GA binding protein transcription factor alpha subunit pseudogene [Source:HGNC Symbol;Acc:HGNC:4072]","synonyms":"E4TF1B,E4TF1,GABPB1","biotype":"processed_pseudogene","ncbi_id":"8327","summary":null,"start":63893286,"end":63894641,"strand":1,"description":"GA binding protein transcription factor alpha subunit pseudogene [Source:HGNC Symbol;Acc:HGNC:4072]"}, {"versioned_ensembl_gene_id":"ENSG00000089693.10","gene_symbol":"MLF2","gene_name":"myeloid leukemia factor 2 [Source:HGNC Symbol;Acc:HGNC:7126]","synonyms":"NTN4","biotype":"protein_coding","ncbi_id":"8079","summary":null,"start":6747996,"end":6767475,"strand":-1,"description":"myeloid leukemia factor 2 [Source:HGNC Symbol;Acc:HGNC:7126]"}, {"versioned_ensembl_gene_id":"ENSG00000236299.7","gene_symbol":"AC092634.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63888200,"end":63900794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230422.1","gene_symbol":"TMPOP1","gene_name":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]","synonyms":"TMPOL1,Em:AB014080.3","biotype":"processed_pseudogene","ncbi_id":"100129772","summary":null,"start":30456357,"end":30457894,"strand":1,"description":"thymopoietin pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21364]"}, {"versioned_ensembl_gene_id":"ENSG00000211752.3","gene_symbol":"TRBV27","gene_name":"T-cell receptor beta variable 27 [Source:HGNC Symbol;Acc:HGNC:12208]","synonyms":"TCRBV27S1,TCRBV14S1","biotype":"TR_V_gene","ncbi_id":"28560","summary":null,"start":142715346,"end":142715861,"strand":1,"description":"T-cell receptor beta variable 27 [Source:HGNC Symbol;Acc:HGNC:12208]"}, {"versioned_ensembl_gene_id":"ENSG00000231276.2","gene_symbol":"E2F4P1","gene_name":"E2F transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131899","summary":null,"start":39553811,"end":39554943,"strand":1,"description":"E2F transcription factor 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38684]"}, {"versioned_ensembl_gene_id":"ENSG00000164627.17","gene_symbol":"KIF6","gene_name":"kinesin family member 6 [Source:HGNC Symbol;Acc:HGNC:21202]","synonyms":"MGC33317,DKFZp451I2418,dJ188D3.1,dJ137F1.4,dJ1043E3.1,C6orf102","biotype":"protein_coding","ncbi_id":"221458","summary":"This gene encodes a member of a family of molecular motors which are involved in intracellular transport of protein complexes, membrane organelles, and messenger ribonucleic acid along microtubules. Kinesins function as homodimeric molecules with two N-terminal head domains that move along microtubules and two C-terminal tail domains that interact with the transported cargo, either directly or indirectly, through adapter molecules. This gene is ubiquitously expressed in coronary arteries and other vascular tissue. A naturally occurring mutation in this gene is associated with coronary heart disease. [provided by RefSeq, May 2017]","start":39329990,"end":39725405,"strand":-1,"description":"kinesin family member 6 [Source:HGNC Symbol;Acc:HGNC:21202]"}, {"versioned_ensembl_gene_id":"ENSG00000284621.1","gene_symbol":"AP000553.3","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":21661859,"end":21661929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207751.3","gene_symbol":"MIR130B","gene_name":"microRNA 130b [Source:HGNC Symbol;Acc:HGNC:31515]","synonyms":"MIRN130B,hsa-mir-130b,MIRN130B,hsa-mir-130b","biotype":"processed_transcript","ncbi_id":"406920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21652270,"end":21670237,"strand":1,"description":"microRNA 130b [Source:HGNC Symbol;Acc:HGNC:31515]"}, {"versioned_ensembl_gene_id":"ENSG00000107562.16","gene_symbol":"CXCL12","gene_name":"C-X-C motif chemokine ligand 12 [Source:HGNC Symbol;Acc:HGNC:10672]","synonyms":"PBSF,TPAR1,TLSF-b,TLSF-a,SDF1B,SDF1A,SDF1,SDF-1b,SDF-1a,SCYB12","biotype":"protein_coding","ncbi_id":"6387","summary":"This antimicrobial gene encodes a stromal cell-derived alpha chemokine member of the intercrine family. The encoded protein functions as the ligand for the G-protein coupled receptor, chemokine (C-X-C motif) receptor 4, and plays a role in many diverse cellular functions, including embryogenesis, immune surveillance, inflammation response, tissue homeostasis, and tumor growth and metastasis. Mutations in this gene are associated with resistance to human immunodeficiency virus type 1 infections. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":44370165,"end":44386493,"strand":-1,"description":"C-X-C motif chemokine ligand 12 [Source:HGNC Symbol;Acc:HGNC:10672]"}, {"versioned_ensembl_gene_id":"ENSG00000232801.1","gene_symbol":"SDCBPP3","gene_name":"syndecan binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44687]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131656","summary":null,"start":40890647,"end":40891537,"strand":-1,"description":"syndecan binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44687]"}, {"versioned_ensembl_gene_id":"ENSG00000235207.1","gene_symbol":"TUBBP6","gene_name":"tubulin beta class I pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42175]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442308","summary":null,"start":55645620,"end":55646951,"strand":1,"description":"tubulin beta class I pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42175]"}, {"versioned_ensembl_gene_id":"ENSG00000100027.14","gene_symbol":"YPEL1","gene_name":"yippee like 1 [Source:HGNC Symbol;Acc:HGNC:12845]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29799","summary":"This gene is located in the region associated with DiGeorge syndrome on chromosome 22. The encoded protein localizes to the centrosome and nucleolus and may play a role in the regulation of cell division. [provided by RefSeq, Feb 2015]","start":21697544,"end":21735834,"strand":-1,"description":"yippee like 1 [Source:HGNC Symbol;Acc:HGNC:12845]"}, {"versioned_ensembl_gene_id":"ENSG00000227755.1","gene_symbol":"AP000344.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":23446598,"end":23460833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172780.16","gene_symbol":"RAB43","gene_name":"RAB43, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:19983]","synonyms":"RAB11B,ISY1,RAB41","biotype":"protein_coding","ncbi_id":"339122","summary":null,"start":129087569,"end":129122801,"strand":-1,"description":"RAB43, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:19983]"}, {"versioned_ensembl_gene_id":"ENSG00000231317.1","gene_symbol":"AC091812.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":55656768,"end":55678490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189145.7","gene_symbol":"AC092268.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40907987,"end":40908391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109270.12","gene_symbol":"LAMTOR3","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 [Source:HGNC Symbol;Acc:HGNC:15606]","synonyms":"Ragulator3,MP1,MAPKSP1,MAPBP,MAP2K1IP1","biotype":"protein_coding","ncbi_id":"8649","summary":"This gene encodes a scaffold protein that functions in the extracellular signal-regulated kinase (ERK) cascade. The protein is localized to late endosomes by the mitogen-activated protein-binding protein-interacting protein, and binds specifically to MAP kinase kinase MAP2K1/MEK1, MAP kinase MAPK3/ERK1, and MAP kinase MAPK1/ERK2. Studies of the orthologous gene in mouse indicate that it regulates late endosomal traffic and cell proliferation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 13. [provided by RefSeq, Aug 2011]","start":99878336,"end":99894490,"strand":-1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 [Source:HGNC Symbol;Acc:HGNC:15606]"}, {"versioned_ensembl_gene_id":"ENSG00000216866.5","gene_symbol":"RPS2P55","gene_name":"ribosomal protein S2 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36140]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286444","summary":null,"start":40934982,"end":40935864,"strand":-1,"description":"ribosomal protein S2 pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:36140]"}, {"versioned_ensembl_gene_id":"ENSG00000236042.2","gene_symbol":"Z74696.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128098032,"end":128098529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007968.6","gene_symbol":"E2F2","gene_name":"E2F transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3114]","synonyms":"E2F-2","biotype":"protein_coding","ncbi_id":"1870","summary":"The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein and another 2 members, E2F1 and E2F3, have an additional cyclin binding domain. This protein binds specifically to retinoblastoma protein pRB in a cell-cycle dependent manner, and it exhibits overall 46% amino acid identity to E2F1. [provided by RefSeq, Jul 2008]","start":23506430,"end":23531220,"strand":-1,"description":"E2F transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3114]"}, {"versioned_ensembl_gene_id":"ENSG00000237931.1","gene_symbol":"CLIC4P3","gene_name":"chloride intracellular channel 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442447","summary":null,"start":41076999,"end":41077750,"strand":1,"description":"chloride intracellular channel 4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49799]"}, {"versioned_ensembl_gene_id":"ENSG00000225545.1","gene_symbol":"AL162399.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170587249,"end":170588236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131650.13","gene_symbol":"KREMEN2","gene_name":"kringle containing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:18797]","synonyms":"MGC10791,KRM2","biotype":"protein_coding","ncbi_id":"79412","summary":"This gene encodes a high-affinity dickkopf homolog 1 (DKK1) transmembrane receptor. A similar protein in mouse functions interacts with with DKK1 to block wingless (WNT)/beta-catenin signaling. The encoded protein forms a ternary membrane complex with DKK1 and the WNT receptor lipoprotein receptor-related protein 6 (LRP6), and induces rapid endocytosis and removal of LRP6 from the plasma membrane. It contains extracellular kringle, WSC, and CUB domains. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":2963944,"end":2968383,"strand":1,"description":"kringle containing transmembrane protein 2 [Source:HGNC Symbol;Acc:HGNC:18797]"}, {"versioned_ensembl_gene_id":"ENSG00000225622.1","gene_symbol":"PPIAP17","gene_name":"peptidylprolyl isomerase A pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:16334]","synonyms":"bA494B22.1,PPIP11","biotype":"processed_pseudogene","ncbi_id":"170540","summary":null,"start":16223750,"end":16224535,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:16334]"}, {"versioned_ensembl_gene_id":"ENSG00000178248.11","gene_symbol":"LINC01658","gene_name":"long intergenic non-protein coding RNA 1658 [Source:HGNC Symbol;Acc:HGNC:52446]","synonyms":null,"biotype":"lincRNA","ncbi_id":"388882","summary":null,"start":23462086,"end":23486980,"strand":-1,"description":"long intergenic non-protein coding RNA 1658 [Source:HGNC Symbol;Acc:HGNC:52446]"}, {"versioned_ensembl_gene_id":"ENSG00000163016.9","gene_symbol":"ALMS1P1","gene_name":"ALMS1, centrosome and basal body associated protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29586]","synonyms":"ALMS1P,ALMS1L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"200420","summary":null,"start":73644919,"end":73685576,"strand":1,"description":"ALMS1, centrosome and basal body associated protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29586]"}, {"versioned_ensembl_gene_id":"ENSG00000238025.1","gene_symbol":"ZDHHC4P1","gene_name":"zinc finger DHHC-type containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39443]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420920","summary":null,"start":42933858,"end":42934892,"strand":1,"description":"zinc finger DHHC-type containing 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39443]"}, {"versioned_ensembl_gene_id":"ENSG00000230187.1","gene_symbol":"AL139109.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70672895,"end":70673515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139239.7","gene_symbol":"AC078814.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62965325,"end":62965969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284630.1","gene_symbol":"AP000553.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":21657811,"end":21661021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133106.14","gene_symbol":"EPSTI1","gene_name":"epithelial stromal interaction 1 [Source:HGNC Symbol;Acc:HGNC:16465]","synonyms":"MGC29634,BRESI1","biotype":"protein_coding","ncbi_id":"94240","summary":"The protein encoded by this gene has been shown to promote tumor invasion and metastasis in some invasive cancer cells when overexpressed. Expression of this gene has been shown to be upregulated by direct binding of the Kruppel like factor 8 protein to promoter sequences. The translated protein interacts with the amino terminal region of the valosin containing protein gene product, resulting in the nuclear translocation of the nuclear factor kappa B subunit 1 gene product, and activation of target genes. Overexpression of this gene has been observed in some breast cancers and in some individuals with systemic lupus erythematosus (SLE). [provided by RefSeq, Sep 2016]","start":42886388,"end":42992271,"strand":-1,"description":"epithelial stromal interaction 1 [Source:HGNC Symbol;Acc:HGNC:16465]"}, {"versioned_ensembl_gene_id":"ENSG00000284651.1","gene_symbol":"AP000553.5","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":21661242,"end":21661295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281743.1","gene_symbol":"AC233280.15","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195650146,"end":195651472,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213747.2","gene_symbol":"AL627390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70857163,"end":70857502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242308.2","gene_symbol":"AC048334.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":112696908,"end":112697706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284654.1","gene_symbol":"AP000553.6","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":21661476,"end":21661593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240893.1","gene_symbol":"LINC02042","gene_name":"long intergenic non-protein coding RNA 2042 [Source:HGNC Symbol;Acc:HGNC:52882]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929694","summary":null,"start":112736447,"end":112749319,"strand":-1,"description":"long intergenic non-protein coding RNA 2042 [Source:HGNC Symbol;Acc:HGNC:52882]"}, {"versioned_ensembl_gene_id":"ENSG00000272954.1","gene_symbol":"AP000553.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":21661934,"end":21662363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281738.1","gene_symbol":"LINC01839","gene_name":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]","synonyms":"EIF2B5-IT1","biotype":"sense_intronic","ncbi_id":"105374251","summary":null,"start":184510148,"end":184513434,"strand":1,"description":"long intergenic non-protein coding RNA 1839 [Source:HGNC Symbol;Acc:HGNC:41330]"}, {"versioned_ensembl_gene_id":"ENSG00000261296.1","gene_symbol":"AC126323.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62274163,"end":62278365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257779.1","gene_symbol":"AC078814.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63002469,"end":63002795,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276075.1","gene_symbol":"AC027682.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67517862,"end":67528675,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225413.2","gene_symbol":"LINC02557","gene_name":"long intergenic non-protein coding RNA 2557 [Source:HGNC Symbol;Acc:HGNC:53596]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372955","summary":null,"start":23512494,"end":23513602,"strand":-1,"description":"long intergenic non-protein coding RNA 2557 [Source:HGNC Symbol;Acc:HGNC:53596]"}, {"versioned_ensembl_gene_id":"ENSG00000204872.4","gene_symbol":"NAT8B","gene_name":"N-acetyltransferase 8B (putative, gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30235]","synonyms":"NAT8BP,Hcml2","biotype":"polymorphic_pseudogene","ncbi_id":"51471","summary":"The protein encoded by this gene is highly similar to the N-acetyltransferase 8 (NAT8) gene product, which is a kidney and liver protein with homology to bacterial acetyltransferases involved in drug resistance. This gene is localized on chromosome 2 in the vicinity of the NAT8 gene and may represent a pseudogene of NAT8. This gene contains two polymorphic nonsense mutations that disrupt the active site of the protein. The full-length product of this gene contains a complete acetyltransferase domain and is identical in length to NAT8. [provided by RefSeq, Jul 2008]","start":73700576,"end":73701340,"strand":-1,"description":"N-acetyltransferase 8B (putative, gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:30235]"}, {"versioned_ensembl_gene_id":"ENSG00000091482.5","gene_symbol":"SMPX","gene_name":"small muscle protein, X-linked [Source:HGNC Symbol;Acc:HGNC:11122]","synonyms":"DFNX4,DFN6","biotype":"protein_coding","ncbi_id":"23676","summary":"This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]","start":21705972,"end":21758163,"strand":-1,"description":"small muscle protein, X-linked [Source:HGNC Symbol;Acc:HGNC:11122]"}, {"versioned_ensembl_gene_id":"ENSG00000280623.1","gene_symbol":"PCAT14","gene_name":"prostate cancer associated transcript 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48977]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101978785","summary":null,"start":23536881,"end":23547797,"strand":1,"description":"prostate cancer associated transcript 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48977]"}, {"versioned_ensembl_gene_id":"ENSG00000260894.1","gene_symbol":"AC027682.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67542304,"end":67542572,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260957.1","gene_symbol":"AC126323.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62284190,"end":62285006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250517.2","gene_symbol":"LDHAL6CP","gene_name":"lactate dehydrogenase A like 6C, pseudogene [Source:HGNC Symbol;Acc:HGNC:39423]","synonyms":"LDH6C","biotype":"transcribed_processed_pseudogene","ncbi_id":"121498","summary":null,"start":63003553,"end":63006902,"strand":1,"description":"lactate dehydrogenase A like 6C, pseudogene [Source:HGNC Symbol;Acc:HGNC:39423]"}, {"versioned_ensembl_gene_id":"ENSG00000261396.1","gene_symbol":"AC027682.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":67538557,"end":67540106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259557.2","gene_symbol":"HMGN1P26","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39370]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128015","summary":null,"start":62362029,"end":62362331,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 26 [Source:HGNC Symbol;Acc:HGNC:39370]"}, {"versioned_ensembl_gene_id":"ENSG00000277199.1","gene_symbol":"LINC01632","gene_name":"long intergenic non-protein coding RNA 1632 [Source:HGNC Symbol;Acc:HGNC:52419]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929826","summary":null,"start":144627192,"end":144642372,"strand":-1,"description":"long intergenic non-protein coding RNA 1632 [Source:HGNC Symbol;Acc:HGNC:52419]"}, {"versioned_ensembl_gene_id":"ENSG00000257235.1","gene_symbol":"AC078814.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63004338,"end":63006541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250962.1","gene_symbol":"AC090568.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88485110,"end":88486094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262231.1","gene_symbol":"AC104770.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":6189361,"end":6190541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271644.1","gene_symbol":"AC242498.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144965025,"end":144965135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278273.1","gene_symbol":"FP700107.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144661200,"end":144679513,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253553.5","gene_symbol":"AC090568.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":88326836,"end":88737134,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273825.1","gene_symbol":"FP700111.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":144754572,"end":144786606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237703.8","gene_symbol":"TRIM10","gene_name":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]","synonyms":"HERF1,RNF9,RFB30","biotype":"protein_coding","ncbi_id":"10107","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to cytoplasmic bodies. Studies in mice suggest that this protein plays a role in terminal differentiation of erythroid cells. Alternate splicing of this gene generates two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30144448,"end":30153436,"strand":-1,"description":"tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]"}, {"versioned_ensembl_gene_id":"ENSG00000128322.6","gene_symbol":"IGLL1","gene_name":"immunoglobulin lambda like polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:5870]","synonyms":"IGVPB,IGLL,IGL5,CD179B,14.1","biotype":"protein_coding","ncbi_id":"3543","summary":"The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":23573125,"end":23580308,"strand":-1,"description":"immunoglobulin lambda like polypeptide 1 [Source:HGNC Symbol;Acc:HGNC:5870]"}, {"versioned_ensembl_gene_id":"ENSG00000171786.5","gene_symbol":"NHLH1","gene_name":"nescient helix-loop-helix 1 [Source:HGNC Symbol;Acc:HGNC:7817]","synonyms":"NSCL1,NSCL,HEN1,bHLHa35","biotype":"protein_coding","ncbi_id":"4807","summary":"The helix-loop-helix (HLH) proteins are a family of putative transcription factors, some of which have been shown to play an important role in growth and development of a wide variety of tissues and species. Four members of this family have been clearly implicated in tumorigenesis via their involvement in chromosomal translocations in lymphoid tumors: MYC (MIM 190080), LYL1 (MIM 151440), E2A (MIM 147141), and SCL (MIM 187040).[supplied by OMIM, Nov 2002]","start":160367067,"end":160372848,"strand":1,"description":"nescient helix-loop-helix 1 [Source:HGNC Symbol;Acc:HGNC:7817]"}, {"versioned_ensembl_gene_id":"ENSG00000226990.1","gene_symbol":"AC025946.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8400860,"end":8461863,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224363.2","gene_symbol":"FP700111.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144641371,"end":144919902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281250.1","gene_symbol":"LINC02054","gene_name":"long intergenic non-protein coding RNA 2054 [Source:HGNC Symbol;Acc:HGNC:52894]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374250","summary":null,"start":184426592,"end":184444693,"strand":1,"description":"long intergenic non-protein coding RNA 2054 [Source:HGNC Symbol;Acc:HGNC:52894]"}, {"versioned_ensembl_gene_id":"ENSG00000242770.2","gene_symbol":"AC092892.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":112802478,"end":112812819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185737.12","gene_symbol":"NRG3","gene_name":"neuregulin 3 [Source:HGNC Symbol;Acc:HGNC:7999]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10718","summary":"This gene is a member of the neuregulin gene family. This gene family encodes ligands for the transmembrane tyrosine kinase receptors ERBB3 and ERBB4 - members of the epidermal growth factor receptor family. Ligand binding activates intracellular signaling cascades and the induction of cellular responses including proliferation, migration, differentiation, and survival or apoptosis. This gene encodes neuregulin 3 (NRG3). NRG3 has been shown to activate the tyrosine phosphorylation of its cognate receptor, ERBB4, and is thought to influence neuroblast proliferation, migration and differentiation by signalling through ERBB4. NRG3 also promotes mammary differentiation during embryogenesis. Linkage studies have implicated this gene as a susceptibility locus for schizophrenia and schizoaffective disorder. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described but their biological validity has not been verified.[provided by RefSeq, Sep 2009]","start":81875314,"end":82987179,"strand":1,"description":"neuregulin 3 [Source:HGNC Symbol;Acc:HGNC:7999]"}, {"versioned_ensembl_gene_id":"ENSG00000100376.11","gene_symbol":"FAM118A","gene_name":"family with sequence similarity 118 member A [Source:HGNC Symbol;Acc:HGNC:1313]","synonyms":"FLJ20635,C22orf8,bK268H5.C22.4","biotype":"protein_coding","ncbi_id":"55007","summary":null,"start":45308968,"end":45341955,"strand":1,"description":"family with sequence similarity 118 member A [Source:HGNC Symbol;Acc:HGNC:1313]"}, {"versioned_ensembl_gene_id":"ENSG00000271251.1","gene_symbol":"AC025946.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8472719,"end":8472952,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223725.6","gene_symbol":"AC009226.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":207239864,"end":207529795,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240804.1","gene_symbol":"NPM1P28","gene_name":"nucleophosmin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:45207]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646849","summary":null,"start":147590996,"end":147591835,"strand":-1,"description":"nucleophosmin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:45207]"}, {"versioned_ensembl_gene_id":"ENSG00000206531.10","gene_symbol":"CD200R1L","gene_name":"CD200 receptor 1 like [Source:HGNC Symbol;Acc:HGNC:24665]","synonyms":"CD200RLa,CD200R2","biotype":"protein_coding","ncbi_id":"344807","summary":null,"start":112815709,"end":112846856,"strand":-1,"description":"CD200 receptor 1 like [Source:HGNC Symbol;Acc:HGNC:24665]"}, {"versioned_ensembl_gene_id":"ENSG00000279788.1","gene_symbol":"CU638689.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6676178,"end":6679962,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259102.2","gene_symbol":"SMARCE1P3","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39733]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401744","summary":null,"start":21162513,"end":21163743,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39733]"}, {"versioned_ensembl_gene_id":"ENSG00000204272.12","gene_symbol":"NBDY","gene_name":"negative regulator of P-body association [Source:HGNC Symbol;Acc:HGNC:50713]","synonyms":"NoBody,LINC01420","biotype":"protein_coding","ncbi_id":"550643","summary":null,"start":56729241,"end":56818380,"strand":1,"description":"negative regulator of P-body association [Source:HGNC Symbol;Acc:HGNC:50713]"}, {"versioned_ensembl_gene_id":"ENSG00000213771.3","gene_symbol":"KRT8P37","gene_name":"keratin 8 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39871]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287325","summary":null,"start":8513687,"end":8515106,"strand":-1,"description":"keratin 8 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:39871]"}, {"versioned_ensembl_gene_id":"ENSG00000273528.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,LILRA5,CD85m,ILT10,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000262609.1","gene_symbol":"AC005668.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6322413,"end":6323228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239661.1","gene_symbol":"AC092925.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147844123,"end":147846657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198736.11","gene_symbol":"MSRB1","gene_name":"methionine sulfoxide reductase B1 [Source:HGNC Symbol;Acc:HGNC:14133]","synonyms":"SEPX1,SepR,SelX,SelR","biotype":"protein_coding","ncbi_id":"51734","summary":"The protein encoded by this gene belongs to the methionine-R-sulfoxide reductase B (MsrB) family. Members of this family function as repair enzymes that protect proteins from oxidative stress by catalyzing the reduction of methionine-R-sulfoxides to methionines. This protein is highly expressed in liver and kidney, and is localized to the nucleus and cytosol. It is the only member of the MsrB family that is a selenoprotein, containing a selenocysteine (Sec) residue at its active site. It also has the highest methionine-R-sulfoxide reductase activity compared to other members containing cysteine in place of Sec. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. A pseudogene of this locus has been identified on chromosome 19. [provided by RefSeq, Aug 2017]","start":1938210,"end":1943326,"strand":-1,"description":"methionine sulfoxide reductase B1 [Source:HGNC Symbol;Acc:HGNC:14133]"}, {"versioned_ensembl_gene_id":"ENSG00000149743.13","gene_symbol":"TRPT1","gene_name":"tRNA phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:20316]","synonyms":"MGC11134","biotype":"protein_coding","ncbi_id":"83707","summary":null,"start":64223799,"end":64226254,"strand":-1,"description":"tRNA phosphotransferase 1 [Source:HGNC Symbol;Acc:HGNC:20316]"}, {"versioned_ensembl_gene_id":"ENSG00000224605.1","gene_symbol":"AL080284.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":91390313,"end":91393000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259882.2","gene_symbol":"AC142384.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33577502,"end":33622547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255420.1","gene_symbol":"CASC23","gene_name":"cancer susceptibility 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50865]","synonyms":"LINC01464","biotype":"antisense_RNA","ncbi_id":"103581031","summary":null,"start":8011278,"end":8016489,"strand":-1,"description":"cancer susceptibility 23 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50865]"}, {"versioned_ensembl_gene_id":"ENSG00000270972.1","gene_symbol":"AC136475.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":333192,"end":333688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233276.3","gene_symbol":"GPX1","gene_name":"glutathione peroxidase 1 [Source:HGNC Symbol;Acc:HGNC:4553]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2876","summary":"The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Other studies indicate that H2O2 is also essential for growth-factor mediated signal transduction, mitochondrial function, and maintenance of thiol redox-balance; therefore, by limiting H2O2 accumulation, glutathione peroxidases are also involved in modulating these processes. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is the most abundant, is ubiquitously expressed and localized in the cytoplasm, and whose preferred substrate is hydrogen peroxide. It is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. This gene contains an in-frame GCG trinucleotide repeat in the coding region, and three alleles with 4, 5 or 6 repeats have been found in the human population. The allele with 4 GCG repeats has been significantly associated with breast cancer risk in premenopausal women. Alternatively spliced transcript variants have been found for this gene. Pseudogenes of this locus have been identified on chromosomes X and 21. [provided by RefSeq, Aug 2017]","start":49357176,"end":49358600,"strand":-1,"description":"glutathione peroxidase 1 [Source:HGNC Symbol;Acc:HGNC:4553]"}, {"versioned_ensembl_gene_id":"ENSG00000224944.1","gene_symbol":"CASC6","gene_name":"cancer susceptibility 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49076]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929083","summary":null,"start":91629915,"end":91690428,"strand":-1,"description":"cancer susceptibility 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49076]"}, {"versioned_ensembl_gene_id":"ENSG00000236420.1","gene_symbol":"CHCHD3P1","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44697]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338591","summary":null,"start":8619933,"end":8620608,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44697]"}, {"versioned_ensembl_gene_id":"ENSG00000224277.5","gene_symbol":"AP000345.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23567064,"end":23573507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258906.2","gene_symbol":"AL157687.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21184341,"end":21184959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277456.1","gene_symbol":"AC245128.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239922.1","gene_symbol":"AC092958.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147940004,"end":148006755,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248850.1","gene_symbol":"AC078867.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":126672106,"end":126673223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262095.1","gene_symbol":"MTATP6P25","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52181]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075203","summary":null,"start":91726810,"end":91727070,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:52181]"}, {"versioned_ensembl_gene_id":"ENSG00000273670.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000279923.1","gene_symbol":"AC022417.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":31558573,"end":31559875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187944.2","gene_symbol":"C2orf66","gene_name":"chromosome 2 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33809]","synonyms":"UNQ6411","biotype":"protein_coding","ncbi_id":"401027","summary":null,"start":196805002,"end":196810276,"strand":-1,"description":"chromosome 2 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:33809]"}, {"versioned_ensembl_gene_id":"ENSG00000147443.12","gene_symbol":"DOK2","gene_name":"docking protein 2 [Source:HGNC Symbol;Acc:HGNC:2991]","synonyms":"p56dok-2,Dok-2","biotype":"protein_coding","ncbi_id":"9046","summary":"The protein encoded by this gene is constitutively tyrosine phosphorylated in hematopoietic progenitors isolated from chronic myelogenous leukemia (CML) patients in the chronic phase. It may be a critical substrate for p210(bcr/abl), a chimeric protein whose presence is associated with CML. This encoded protein binds p120 (RasGAP) from CML cells. [provided by RefSeq, Jul 2008]","start":21908873,"end":21913860,"strand":-1,"description":"docking protein 2 [Source:HGNC Symbol;Acc:HGNC:2991]"}, {"versioned_ensembl_gene_id":"ENSG00000258441.1","gene_symbol":"LINC00641","gene_name":"long intergenic non-protein coding RNA 641 [Source:HGNC Symbol;Acc:HGNC:27511]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"283624","summary":null,"start":21200079,"end":21206900,"strand":-1,"description":"long intergenic non-protein coding RNA 641 [Source:HGNC Symbol;Acc:HGNC:27511]"}, {"versioned_ensembl_gene_id":"ENSG00000260518.1","gene_symbol":"BMS1P8","gene_name":"BMS1, ribosome biogenesis factor pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49152]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653557","summary":null,"start":33687025,"end":33698504,"strand":-1,"description":"BMS1, ribosome biogenesis factor pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:49152]"}, {"versioned_ensembl_gene_id":"ENSG00000110987.8","gene_symbol":"BCL7A","gene_name":"BCL tumor suppressor 7A [Source:HGNC Symbol;Acc:HGNC:1004]","synonyms":"BCL7","biotype":"protein_coding","ncbi_id":"605","summary":"This gene is directly involved, with Myc and IgH, in a three-way gene translocation in a Burkitt lymphoma cell line. As a result of the gene translocation, the N-terminal region of the gene product is disrupted, which is thought to be related to the pathogenesis of a subset of high-grade B cell non-Hodgkin lymphoma. The N-terminal segment involved in the translocation includes the region that shares a strong sequence similarity with those of BCL7B and BCL7C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":122019422,"end":122062044,"strand":1,"description":"BCL tumor suppressor 7A [Source:HGNC Symbol;Acc:HGNC:1004]"}, {"versioned_ensembl_gene_id":"ENSG00000204271.12","gene_symbol":"SPIN3","gene_name":"spindlin family member 3 [Source:HGNC Symbol;Acc:HGNC:27272]","synonyms":"TDRD27","biotype":"protein_coding","ncbi_id":"169981","summary":null,"start":56818298,"end":56995827,"strand":-1,"description":"spindlin family member 3 [Source:HGNC Symbol;Acc:HGNC:27272]"}, {"versioned_ensembl_gene_id":"ENSG00000258096.1","gene_symbol":"AC025031.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":46371463,"end":46373778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219087.2","gene_symbol":"MTND4LP19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42253]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075241","summary":null,"start":91727159,"end":91727324,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42253]"}, {"versioned_ensembl_gene_id":"ENSG00000134294.13","gene_symbol":"SLC38A2","gene_name":"solute carrier family 38 member 2 [Source:HGNC Symbol;Acc:HGNC:13448]","synonyms":"SNAT2,SAT2,KIAA1382,ATA2","biotype":"protein_coding","ncbi_id":"54407","summary":null,"start":46358189,"end":46372867,"strand":-1,"description":"solute carrier family 38 member 2 [Source:HGNC Symbol;Acc:HGNC:13448]"}, {"versioned_ensembl_gene_id":"ENSG00000220340.1","gene_symbol":"MTCO1P56","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:52121]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075286","summary":null,"start":91727282,"end":91727505,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:52121]"}, {"versioned_ensembl_gene_id":"ENSG00000276647.1","gene_symbol":"AL773604.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44686358,"end":44686629,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180354.15","gene_symbol":"MTURN","gene_name":"maturin, neural progenitor differentiation regulator homolog [Source:HGNC Symbol;Acc:HGNC:25457]","synonyms":"FLJ25903,Ells1,C7orf41","biotype":"protein_coding","ncbi_id":"222166","summary":null,"start":30134810,"end":30162762,"strand":1,"description":"maturin, neural progenitor differentiation regulator homolog [Source:HGNC Symbol;Acc:HGNC:25457]"}, {"versioned_ensembl_gene_id":"ENSG00000123146.19","gene_symbol":"ADGRE5","gene_name":"adhesion G protein-coupled receptor E5 [Source:HGNC Symbol;Acc:HGNC:1711]","synonyms":"TM7LN1,CD97","biotype":"protein_coding","ncbi_id":"976","summary":"This gene encodes a member of the EGF-TM7 subfamily of adhesion G protein-coupled receptors, which mediate cell-cell interactions. These proteins are cleaved by self-catalytic proteolysis into a large extracellular subunit and seven-span transmembrane subunit, which associate at the cell surface as a receptor complex. The encoded protein may play a role in cell adhesion as well as leukocyte recruitment, activation and migration, and contains multiple extracellular EGF-like repeats which mediate binding to chondroitin sulfate and the cell surface complement regulatory protein CD55. Expression of this gene may play a role in the progression of several types of cancer. Alternatively spliced transcript variants encoding multiple isoforms with 3 to 5 EGF-like repeats have been observed for this gene. This gene is found in a cluster with other EGF-TM7 genes on the short arm of chromosome 19. [provided by RefSeq, Jun 2011]","start":14380501,"end":14408725,"strand":1,"description":"adhesion G protein-coupled receptor E5 [Source:HGNC Symbol;Acc:HGNC:1711]"}, {"versioned_ensembl_gene_id":"ENSG00000175894.14","gene_symbol":"TSPEAR","gene_name":"thrombospondin type laminin G domain and EAR repeats [Source:HGNC Symbol;Acc:HGNC:1268]","synonyms":"TSP-EAR,MGC11251,DFNB98,C21orf29","biotype":"protein_coding","ncbi_id":"54084","summary":"This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":44497892,"end":44711580,"strand":-1,"description":"thrombospondin type laminin G domain and EAR repeats [Source:HGNC Symbol;Acc:HGNC:1268]"}, {"versioned_ensembl_gene_id":"ENSG00000278656.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54836668,"end":54853397,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000237865.3","gene_symbol":"SUCLA2P1","gene_name":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]","synonyms":"Em:AB014080.4,SUCLA2P","biotype":"processed_pseudogene","ncbi_id":"646520","summary":null,"start":30458704,"end":30460073,"strand":1,"description":"succinate-CoA ligase ADP-forming beta subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21632]"}, {"versioned_ensembl_gene_id":"ENSG00000257664.1","gene_symbol":"AC078814.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63055275,"end":63055765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240682.9","gene_symbol":"ISY1","gene_name":"ISY1 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:29201]","synonyms":"KIAA1160,fSAP33","biotype":"protein_coding","ncbi_id":"57461","summary":null,"start":129127415,"end":129161293,"strand":-1,"description":"ISY1 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:29201]"}, {"versioned_ensembl_gene_id":"ENSG00000221883.2","gene_symbol":"ARIH2OS","gene_name":"ariadne RBR E3 ubiquitin protein ligase 2 opposite strand [Source:HGNC Symbol;Acc:HGNC:34425]","synonyms":"C3orf71","biotype":"protein_coding","ncbi_id":"646450","summary":null,"start":48917788,"end":48919385,"strand":-1,"description":"ariadne RBR E3 ubiquitin protein ligase 2 opposite strand [Source:HGNC Symbol;Acc:HGNC:34425]"}, {"versioned_ensembl_gene_id":"ENSG00000137321.7","gene_symbol":"RANP1","gene_name":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]","synonyms":"Em:AB014080.2","biotype":"processed_pseudogene","ncbi_id":"221547","summary":null,"start":30478177,"end":30478827,"strand":1,"description":"RAN, member RAS oncogene family pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21631]"}, {"versioned_ensembl_gene_id":"ENSG00000280176.1","gene_symbol":"AC012486.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":196831975,"end":196832190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204420.8","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"C6orf25,G6b-B,G6b,NG31","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31718594,"end":31726714,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000228357.2","gene_symbol":"HSD17B8","gene_name":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]","synonyms":"SDR30C1,HKE6,D6S2245E,RING2,H2-KE6,KE6,FABGL","biotype":"protein_coding","ncbi_id":"7923","summary":"In mice, the Ke6 protein is a 17-beta-hydroxysteroid dehydrogenase that can regulate the concentration of biologically active estrogens and androgens. It is preferentially an oxidative enzyme and inactivates estradiol, testosterone, and dihydrotestosterone. However, the enzyme has some reductive activity and can synthesize estradiol from estrone. The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily. An alternatively spliced transcript of this gene has been detected, but the full-length nature of this variant has not been determined. [provided by RefSeq, Jul 2008]","start":33358522,"end":33360715,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]"}, {"versioned_ensembl_gene_id":"ENSG00000178149.16","gene_symbol":"DALRD3","gene_name":"DALR anticodon binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25536]","synonyms":"FLJ10496","biotype":"protein_coding","ncbi_id":"55152","summary":"The exact function of this gene is not known. It encodes a protein with a DALR anticodon binding domain similar to that of class Ia aminoacyl tRNA synthetases. This gene is located in a cluster of genes (with a complex sense-anti-sense genome architecture) on chromosome 3, and contains two micro RNA (miRNA) precursors (mir-425 and mir-191) in one of its introns. Preferential expression of this gene (the miRNAs and other genes in the cluster) in testis suggests a role of this gene in spermatogenesis (PMID:19906709). [provided by RefSeq, Feb 2013]","start":49015488,"end":49022293,"strand":-1,"description":"DALR anticodon binding domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25536]"}, {"versioned_ensembl_gene_id":"ENSG00000204362.6","gene_symbol":"AL590644.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17189783,"end":17197617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077327.15","gene_symbol":"SPAG6","gene_name":"sperm associated antigen 6 [Source:HGNC Symbol;Acc:HGNC:11215]","synonyms":"Repro-SA-1,pf16,CT141","biotype":"protein_coding","ncbi_id":"9576","summary":"The correlation of anti-sperm antibodies with cases of unexplained infertility implicates a role for these antibodies in blocking fertilization. Improved diagnosis and treatment of immunologic infertility, as well as identification of proteins for targeted contraception, are dependent on the identification and characterization of relevant sperm antigens. The protein expressed by this gene is recognized by anti-sperm antibodies from an infertile man. This protein localizes to the tail of permeabilized human sperm and contains eight contiguous armadillo repeats, a motif known to mediate protein-protein interactions. Studies in mice suggest that this protein is involved in sperm flagellar motility and maintenance of the structural integrity of mature sperm. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":22345445,"end":22454224,"strand":1,"description":"sperm associated antigen 6 [Source:HGNC Symbol;Acc:HGNC:11215]"}, {"versioned_ensembl_gene_id":"ENSG00000282843.1","gene_symbol":"AL590644.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17193232,"end":17201733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281197.2","gene_symbol":"TNFRSF14-AS1","gene_name":"TNFRSF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26966]","synonyms":"ENST00000416860.2","biotype":"antisense_RNA","ncbi_id":"115110","summary":null,"start":2549920,"end":2557031,"strand":-1,"description":"TNFRSF14 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26966]"}, {"versioned_ensembl_gene_id":"ENSG00000233124.1","gene_symbol":"LINC00456","gene_name":"long intergenic non-protein coding RNA 456 [Source:HGNC Symbol;Acc:HGNC:42804]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103625683","summary":null,"start":97172469,"end":97179622,"strand":-1,"description":"long intergenic non-protein coding RNA 456 [Source:HGNC Symbol;Acc:HGNC:42804]"}, {"versioned_ensembl_gene_id":"ENSG00000143171.12","gene_symbol":"RXRG","gene_name":"retinoid X receptor gamma [Source:HGNC Symbol;Acc:HGNC:10479]","synonyms":"NR2B3","biotype":"protein_coding","ncbi_id":"6258","summary":"This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the antiproliferative effects of retinoic acid (RA). This receptor forms dimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene is expressed at significantly lower levels in non-small cell lung cancer cells. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2010]","start":165400917,"end":165445355,"strand":-1,"description":"retinoid X receptor gamma [Source:HGNC Symbol;Acc:HGNC:10479]"}, {"versioned_ensembl_gene_id":"ENSG00000142623.9","gene_symbol":"PADI1","gene_name":"peptidyl arginine deiminase 1 [Source:HGNC Symbol;Acc:HGNC:18367]","synonyms":"PDI1,PDI,PAD1,HPAD10","biotype":"protein_coding","ncbi_id":"29943","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type I enzyme is involved in the late stages of epidermal differentiation, where it deiminates filaggrin and keratin K1, which maintains hydration of the stratum corneum, and hence the cutaneous barrier function. This enzyme may also play a role in hair follicle formation. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17205126,"end":17246005,"strand":1,"description":"peptidyl arginine deiminase 1 [Source:HGNC Symbol;Acc:HGNC:18367]"}, {"versioned_ensembl_gene_id":"ENSG00000028528.14","gene_symbol":"SNX1","gene_name":"sorting nexin 1 [Source:HGNC Symbol;Acc:HGNC:11172]","synonyms":"Vps5,SNX1A,MGC8664,HsT17379","biotype":"protein_coding","ncbi_id":"6642","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This endosomal protein regulates the cell-surface expression of epidermal growth factor receptor. This protein also has a role in sorting protease-activated receptor-1 from early endosomes to lysosomes. This protein may form oligomeric complexes with family members. This gene results in three transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":64094123,"end":64146090,"strand":1,"description":"sorting nexin 1 [Source:HGNC Symbol;Acc:HGNC:11172]"}, {"versioned_ensembl_gene_id":"ENSG00000248924.2","gene_symbol":"AC139713.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":143555082,"end":143555583,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255856.2","gene_symbol":"AC069503.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":122007434,"end":122020063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183513.8","gene_symbol":"COA5","gene_name":"cytochrome c oxidase assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:33848]","synonyms":"Pet191,MGC52110,FLJ27524,C2orf64","biotype":"protein_coding","ncbi_id":"493753","summary":"This gene encodes an ortholog of yeast Pet191, which in yeast is a subunit of a large oligomeric complex associated with the mitochondrial inner membrane, and required for the assembly of the cytochrome c oxidase complex. Mutations in this gene are associated with mitochondrial complex IV deficiency, a disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to a severe disease affecting several tissues and organs. [provided by RefSeq, Dec 2011]","start":98599310,"end":98608515,"strand":-1,"description":"cytochrome c oxidase assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:33848]"}, {"versioned_ensembl_gene_id":"ENSG00000245112.2","gene_symbol":"SMARCA5-AS1","gene_name":"SMARCA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39982]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128055","summary":null,"start":143513472,"end":143514635,"strand":-1,"description":"SMARCA5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39982]"}, {"versioned_ensembl_gene_id":"ENSG00000251660.1","gene_symbol":"AC007036.3","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":30157531,"end":30159534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230751.1","gene_symbol":"AC007036.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":30140870,"end":30141417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261796.1","gene_symbol":"ISY1-RAB43","gene_name":"ISY1-RAB43 readthrough [Source:HGNC Symbol;Acc:HGNC:42969]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100534599","summary":"This locus represents naturally occurring read-through transcription between the neighboring ISY1 (ISY1 splicing factor homolog) and RAB43 (RAB43, member RAS oncogene family) gene on chromosome 3. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product, but its C-terminus is distinct due to a frameshift relative to the downstream gene. [provided by RefSeq, Mar 2011]","start":129087575,"end":129161036,"strand":-1,"description":"ISY1-RAB43 readthrough [Source:HGNC Symbol;Acc:HGNC:42969]"}, {"versioned_ensembl_gene_id":"ENSG00000153147.5","gene_symbol":"SMARCA5","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 [Source:HGNC Symbol;Acc:HGNC:11101]","synonyms":"ISWI,hSNF2H,hISWI","biotype":"protein_coding","ncbi_id":"8467","summary":"The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The protein encoded by this gene is a component of the chromatin remodeling and spacing factor RSF, a facilitator of the transcription of class II genes by RNA polymerase II. The encoded protein is similar in sequence to the Drosophila ISWI chromatin remodeling protein. [provided by RefSeq, Jul 2008]","start":143513463,"end":143557486,"strand":1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 [Source:HGNC Symbol;Acc:HGNC:11101]"}, {"versioned_ensembl_gene_id":"ENSG00000054523.17","gene_symbol":"KIF1B","gene_name":"kinesin family member 1B [Source:HGNC Symbol;Acc:HGNC:16636]","synonyms":"CMT2A,CMT2,KLP,KIAA0591,HMSNII","biotype":"protein_coding","ncbi_id":"23095","summary":"This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1. [provided by RefSeq, Jul 2008]","start":10210805,"end":10381603,"strand":1,"description":"kinesin family member 1B [Source:HGNC Symbol;Acc:HGNC:16636]"}, {"versioned_ensembl_gene_id":"ENSG00000154813.9","gene_symbol":"DPH3","gene_name":"diphthamide biosynthesis 3 [Source:HGNC Symbol;Acc:HGNC:27717]","synonyms":"ZCSL2,MGC20197,KTI11,DPH3A,DESR1,DELGIP1,DELGIP","biotype":"protein_coding","ncbi_id":"285381","summary":"This gene encodes a CSL zinc finger-containing protein that is required for dipthamide biosynthesis. The encoded protein is necessary for the initial step in the modification of a histidine residue in elongation factor-2 to diphthamide. This modified residue is a target for ADP ribosylation by the bacterial toxins diphtheria toxin and Pseudomonas exotoxin A. Alternative splicing results in multiple transcript variants that encode the same isoform. [provided by RefSeq, Feb 2009]","start":16257978,"end":16264972,"strand":-1,"description":"diphthamide biosynthesis 3 [Source:HGNC Symbol;Acc:HGNC:27717]"}, {"versioned_ensembl_gene_id":"ENSG00000273936.4","gene_symbol":"TNFRSF14","gene_name":"TNF receptor superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11912]","synonyms":"TR2,LIGHTR,HVEM,HVEA,CD270,ATAR","biotype":"protein_coding","ncbi_id":"8764","summary":"This gene encodes a member of the TNF (tumor necrosis factor) receptor superfamily. The encoded protein functions in signal transduction pathways that activate inflammatory and inhibitory T-cell immune response. It binds herpes simplex virus (HSV) viral envelope glycoprotein D (gD), mediating its entry into cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":2555639,"end":2565622,"strand":1,"description":"TNF receptor superfamily member 14 [Source:HGNC Symbol;Acc:HGNC:11912]"}, {"versioned_ensembl_gene_id":"ENSG00000218986.1","gene_symbol":"AL136087.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39353747,"end":39354172,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229395.1","gene_symbol":"AC062039.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":192629919,"end":192645706,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232227.5","gene_symbol":"AC013401.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":192644102,"end":192645387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166148.3","gene_symbol":"AVPR1A","gene_name":"arginine vasopressin receptor 1A [Source:HGNC Symbol;Acc:HGNC:895]","synonyms":"AVPR1","biotype":"protein_coding","ncbi_id":"552","summary":"The protein encoded by this gene acts as receptor for arginine vasopressin. This receptor belongs to the subfamily of G-protein coupled receptors which includes AVPR1B, V2R and OXT receptors. Its activity is mediated by G proteins which stimulate a phosphatidylinositol-calcium second messenger system. The receptor mediates cell contraction and proliferation, platelet aggregation, release of coagulation factor and glycogenolysis. [provided by RefSeq, Jul 2008]","start":63142759,"end":63150942,"strand":-1,"description":"arginine vasopressin receptor 1A [Source:HGNC Symbol;Acc:HGNC:895]"}, {"versioned_ensembl_gene_id":"ENSG00000169241.17","gene_symbol":"SLC50A1","gene_name":"solute carrier family 50 member 1 [Source:HGNC Symbol;Acc:HGNC:30657]","synonyms":"SWEET1,slv,SCP,RZPDo834D038D,RP11-540D14.5,RAG1AP1,HsSWEET1","biotype":"protein_coding","ncbi_id":"55974","summary":null,"start":155135344,"end":155138857,"strand":1,"description":"solute carrier family 50 member 1 [Source:HGNC Symbol;Acc:HGNC:30657]"}, {"versioned_ensembl_gene_id":"ENSG00000176826.15","gene_symbol":"FKBP9P1","gene_name":"FK506 binding protein 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23568]","synonyms":"MGC20531,FKBP9L","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"360132","summary":null,"start":55681074,"end":55713252,"strand":-1,"description":"FK506 binding protein 9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23568]"}, {"versioned_ensembl_gene_id":"ENSG00000261614.1","gene_symbol":"AC106730.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31568386,"end":31569475,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224693.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29887842,"end":29888973,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000228649.8","gene_symbol":"SNHG26","gene_name":"small nucleolar RNA host gene 26 [Source:HGNC Symbol;Acc:HGNC:53131]","synonyms":"AC005682.5","biotype":"processed_transcript","ncbi_id":"109729180","summary":null,"start":22854178,"end":22861579,"strand":1,"description":"small nucleolar RNA host gene 26 [Source:HGNC Symbol;Acc:HGNC:53131]"}, {"versioned_ensembl_gene_id":"ENSG00000279444.1","gene_symbol":"AC135584.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":63151065,"end":63154006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235360.2","gene_symbol":"C6orf47","gene_name":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]","synonyms":"G4,D6S53E","biotype":"protein_coding","ncbi_id":"57827","summary":null,"start":31645706,"end":31648178,"strand":-1,"description":"chromosome 6 open reading frame 47 [Source:HGNC Symbol;Acc:HGNC:19076]"}, {"versioned_ensembl_gene_id":"ENSG00000235052.1","gene_symbol":"AL021154.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23549139,"end":23550915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257332.1","gene_symbol":"HNRNPA1P69","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:48799]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105369973","summary":null,"start":63271404,"end":63272336,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:48799]"}, {"versioned_ensembl_gene_id":"ENSG00000235516.1","gene_symbol":"C6orf47-AS1","gene_name":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"106480731","summary":null,"start":31645737,"end":31648128,"strand":1,"description":"C6orf47 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39767]"}, {"versioned_ensembl_gene_id":"ENSG00000139793.18","gene_symbol":"MBNL2","gene_name":"muscleblind like splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:16746]","synonyms":"MBLL39,MBLL","biotype":"protein_coding","ncbi_id":"10150","summary":"This gene is a member of the muscleblind protein family which was initially described in Drosophila melanogaster. This gene encodes a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. [provided by RefSeq, Mar 2012]","start":97221434,"end":97394120,"strand":1,"description":"muscleblind like splicing regulator 2 [Source:HGNC Symbol;Acc:HGNC:16746]"}, {"versioned_ensembl_gene_id":"ENSG00000261524.1","gene_symbol":"ABCB10P3","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31129]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728248","summary":null,"start":28402868,"end":28405033,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:31129]"}, {"versioned_ensembl_gene_id":"ENSG00000258117.2","gene_symbol":"AC026116.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63292625,"end":63360037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225738.2","gene_symbol":"NRG3-AS1","gene_name":"NRG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31429]","synonyms":"Em:AC010157.1,C10orf100","biotype":"processed_transcript","ncbi_id":"101929590","summary":null,"start":82228985,"end":82232920,"strand":-1,"description":"NRG3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31429]"}, {"versioned_ensembl_gene_id":"ENSG00000272733.1","gene_symbol":"AP000345.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23580880,"end":23583859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276928.1","gene_symbol":"AC091304.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28416449,"end":28416674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278655.1","gene_symbol":"AP000346.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23607041,"end":23608407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253235.1","gene_symbol":"AC111149.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73368770,"end":73369295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235890.2","gene_symbol":"TSPEAR-AS1","gene_name":"TSPEAR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1271]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"54082","summary":null,"start":44506807,"end":44516575,"strand":1,"description":"TSPEAR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1271]"}, {"versioned_ensembl_gene_id":"ENSG00000224269.1","gene_symbol":"AP000697.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36698773,"end":36701564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150048.10","gene_symbol":"CLEC1A","gene_name":"C-type lectin domain family 1 member A [Source:HGNC Symbol;Acc:HGNC:24355]","synonyms":"MGC34328,CLEC1","biotype":"protein_coding","ncbi_id":"51267","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The encoded protein may play a role in regulating dendritic cell function. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":10069554,"end":10111627,"strand":-1,"description":"C-type lectin domain family 1 member A [Source:HGNC Symbol;Acc:HGNC:24355]"}, {"versioned_ensembl_gene_id":"ENSG00000231324.1","gene_symbol":"AP000696.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36632681,"end":36637033,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229458.2","gene_symbol":"AC010157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82224213,"end":82229179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279728.1","gene_symbol":"CU638689.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6712596,"end":6716361,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224376.1","gene_symbol":"AC017104.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":231388976,"end":231394991,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221837.5","gene_symbol":"KRTAP10-9","gene_name":"keratin associated protein 10-9 [Source:HGNC Symbol;Acc:HGNC:22971]","synonyms":"KRTAP18-9,KAP18.9,KAP10.9","biotype":"protein_coding","ncbi_id":"386676","summary":null,"start":44627123,"end":44628293,"strand":1,"description":"keratin associated protein 10-9 [Source:HGNC Symbol;Acc:HGNC:22971]"}, {"versioned_ensembl_gene_id":"ENSG00000165487.13","gene_symbol":"MICU2","gene_name":"mitochondrial calcium uptake 2 [Source:HGNC Symbol;Acc:HGNC:31830]","synonyms":"EFHA1","biotype":"protein_coding","ncbi_id":"221154","summary":null,"start":21492691,"end":21604214,"strand":-1,"description":"mitochondrial calcium uptake 2 [Source:HGNC Symbol;Acc:HGNC:31830]"}, {"versioned_ensembl_gene_id":"ENSG00000274532.1","gene_symbol":"AC091304.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28422172,"end":28422373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130349.9","gene_symbol":"C6orf203","gene_name":"chromosome 6 open reading frame 203 [Source:HGNC Symbol;Acc:HGNC:17971]","synonyms":"PRED31,HSPC230","biotype":"protein_coding","ncbi_id":"51250","summary":null,"start":107028213,"end":107051342,"strand":1,"description":"chromosome 6 open reading frame 203 [Source:HGNC Symbol;Acc:HGNC:17971]"}, {"versioned_ensembl_gene_id":"ENSG00000089177.18","gene_symbol":"KIF16B","gene_name":"kinesin family member 16B [Source:HGNC Symbol;Acc:HGNC:15869]","synonyms":"SNX23,FLJ20135,dJ971B4.1,C20orf23","biotype":"protein_coding","ncbi_id":"55614","summary":"The protein encoded by this gene is a kinesin-like protein that may be involved in intracellular trafficking. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]","start":16272104,"end":16573434,"strand":-1,"description":"kinesin family member 16B [Source:HGNC Symbol;Acc:HGNC:15869]"}, {"versioned_ensembl_gene_id":"ENSG00000284628.1","gene_symbol":"AC091304.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28444144,"end":28444264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224569.3","gene_symbol":"AC095052.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":13977166,"end":13978028,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241123.1","gene_symbol":"KRTAP10-5","gene_name":"keratin associated protein 10-5 [Source:HGNC Symbol;Acc:HGNC:22969]","synonyms":"KRTAP18-5,KAP18.5,KAP10.5","biotype":"protein_coding","ncbi_id":"386680","summary":"This is an intronless gene located in a cluster of related genes on the q arm of chromosome 21. The proteins encoded by these genes form disulfide bonds with cysteine residues in hair keratins, thereby contributing to the structure and stability of hair fibers. [provided by RefSeq, Apr 2014]","start":44579455,"end":44580604,"strand":-1,"description":"keratin associated protein 10-5 [Source:HGNC Symbol;Acc:HGNC:22969]"}, {"versioned_ensembl_gene_id":"ENSG00000226329.2","gene_symbol":"AC005682.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22863874,"end":22881350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159263.15","gene_symbol":"SIM2","gene_name":"single-minded family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10883]","synonyms":"SIM,MGC119447,bHLHe15","biotype":"protein_coding","ncbi_id":"6493","summary":"This gene represents a homolog of the Drosophila single-minded (sim) gene, which encodes a transcription factor that is a master regulator of neurogenesis. The encoded protein is ubiquitinated by RING-IBR-RING-type E3 ubiquitin ligases, including the parkin RBR E3 ubiquitin protein ligase. This gene maps within the so-called Down syndrome chromosomal region, and is thus thought to contribute to some specific Down syndrome phenotypes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]","start":36699133,"end":36749917,"strand":1,"description":"single-minded family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:10883]"}, {"versioned_ensembl_gene_id":"ENSG00000243489.4","gene_symbol":"KRTAP10-11","gene_name":"keratin associated protein 10-11 [Source:HGNC Symbol;Acc:HGNC:20528]","synonyms":"KRTAP18.11,KRTAP18-11,KAP18.11,KAP10.11","biotype":"protein_coding","ncbi_id":"386678","summary":null,"start":44646414,"end":44647650,"strand":1,"description":"keratin associated protein 10-11 [Source:HGNC Symbol;Acc:HGNC:20528]"}, {"versioned_ensembl_gene_id":"ENSG00000229880.1","gene_symbol":"IMMTP1","gene_name":"inner membrane mitochondrial protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6048]","synonyms":"IMMTP","biotype":"processed_pseudogene","ncbi_id":"54045","summary":null,"start":44675868,"end":44678086,"strand":-1,"description":"inner membrane mitochondrial protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6048]"}, {"versioned_ensembl_gene_id":"ENSG00000260159.1","gene_symbol":"AC091304.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28454660,"end":28457783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212933.1","gene_symbol":"KRTAP12-4","gene_name":"keratin associated protein 12-4 [Source:HGNC Symbol;Acc:HGNC:20532]","synonyms":"KRTAP12.4","biotype":"protein_coding","ncbi_id":"386684","summary":null,"start":44654213,"end":44654659,"strand":-1,"description":"keratin associated protein 12-4 [Source:HGNC Symbol;Acc:HGNC:20532]"}, {"versioned_ensembl_gene_id":"ENSG00000215454.6","gene_symbol":"KRTAP10-4","gene_name":"keratin associated protein 10-4 [Source:HGNC Symbol;Acc:HGNC:20521]","synonyms":"KRTAP18.4,KRTAP18-4,KAP10.4","biotype":"protein_coding","ncbi_id":"386672","summary":"This is an intronless gene located in a cluster of related genes on the q arm of chromosome 21. The proteins encoded by these genes form disulfide bonds with cysteine residues in hair keratins, thereby contributing to the structure and stability of hair fibers. [provided by RefSeq, Apr 2014]","start":44573724,"end":44638284,"strand":1,"description":"keratin associated protein 10-4 [Source:HGNC Symbol;Acc:HGNC:20521]"}, {"versioned_ensembl_gene_id":"ENSG00000265511.1","gene_symbol":"AC020558.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17507351,"end":17508308,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219284.2","gene_symbol":"AL592291.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127632958,"end":127635321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092096.16","gene_symbol":"SLC22A17","gene_name":"solute carrier family 22 member 17 [Source:HGNC Symbol;Acc:HGNC:23095]","synonyms":"NGALR,BOIT,BOCT","biotype":"protein_coding","ncbi_id":"51310","summary":null,"start":23346306,"end":23352912,"strand":-1,"description":"solute carrier family 22 member 17 [Source:HGNC Symbol;Acc:HGNC:23095]"}, {"versioned_ensembl_gene_id":"ENSG00000151164.18","gene_symbol":"RAD9B","gene_name":"RAD9 checkpoint clamp component B [Source:HGNC Symbol;Acc:HGNC:21700]","synonyms":"FLJ40346","biotype":"protein_coding","ncbi_id":"144715","summary":null,"start":110501655,"end":110532086,"strand":1,"description":"RAD9 checkpoint clamp component B [Source:HGNC Symbol;Acc:HGNC:21700]"}, {"versioned_ensembl_gene_id":"ENSG00000218187.2","gene_symbol":"AL356432.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127654860,"end":127655278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235303.1","gene_symbol":"AL023495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170598854,"end":170647339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230797.2","gene_symbol":"YY2","gene_name":"YY2 transcription factor [Source:HGNC Symbol;Acc:HGNC:31684]","synonyms":"ZNF631","biotype":"protein_coding","ncbi_id":"404281","summary":"The protein encoded by this gene is a transcription factor that includes several Kruppel-like zinc fingers in its C-terminal region. It possesses both activation and repression domains, and it can therefore have both positive and negative effects on the transcription of target genes. This gene has an intronless coding region, and it appears to have arisen by retrotransposition of the related YY1 transcription factor gene, which is located on chromosome 14. [provided by RefSeq, May 2010]","start":21855987,"end":21858727,"strand":1,"description":"YY2 transcription factor [Source:HGNC Symbol;Acc:HGNC:31684]"}, {"versioned_ensembl_gene_id":"ENSG00000260212.1","gene_symbol":"AL356432.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127659424,"end":127660338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221864.4","gene_symbol":"KRTAP12-2","gene_name":"keratin associated protein 12-2 [Source:HGNC Symbol;Acc:HGNC:20530]","synonyms":"KAP12.2,KRTAP12.2","biotype":"protein_coding","ncbi_id":"353323","summary":null,"start":44666189,"end":44666927,"strand":-1,"description":"keratin associated protein 12-2 [Source:HGNC Symbol;Acc:HGNC:20530]"}, {"versioned_ensembl_gene_id":"ENSG00000214089.3","gene_symbol":"RPL9P21","gene_name":"ribosomal protein L9 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35886]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728374","summary":null,"start":44414649,"end":44415153,"strand":-1,"description":"ribosomal protein L9 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:35886]"}, {"versioned_ensembl_gene_id":"ENSG00000012174.11","gene_symbol":"MBTPS2","gene_name":"membrane bound transcription factor peptidase, site 2 [Source:HGNC Symbol;Acc:HGNC:15455]","synonyms":"S2P,KFSD","biotype":"protein_coding","ncbi_id":"51360","summary":"This gene encodes a intramembrane zinc metalloprotease, which is essential in development. This protease functions in the signal protein activation involved in sterol control of transcription and the ER stress response. Mutations in this gene have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome); IFAP syndrome has been quantitatively linked to a reduction in cholesterol homeostasis and ER stress response.[provided by RefSeq, Aug 2009]","start":21839636,"end":21885424,"strand":1,"description":"membrane bound transcription factor peptidase, site 2 [Source:HGNC Symbol;Acc:HGNC:15455]"}, {"versioned_ensembl_gene_id":"ENSG00000219699.2","gene_symbol":"AL356432.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127659690,"end":127660579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215455.4","gene_symbol":"KRTAP10-1","gene_name":"keratin associated protein 10-1 [Source:HGNC Symbol;Acc:HGNC:22966]","synonyms":"KAP18.1,KAP10.1,KRTAP18-1","biotype":"protein_coding","ncbi_id":"386677","summary":"This gene encodes a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This gene encodes a member of the high sulfur KAP family. It is localized to a cluster of intronless KAPs at 21q22.3 which are located within the introns of the C21orf29 gene. [provided by RefSeq, Jul 2008]","start":44538981,"end":44540195,"strand":-1,"description":"keratin associated protein 10-1 [Source:HGNC Symbol;Acc:HGNC:22966]"}, {"versioned_ensembl_gene_id":"ENSG00000117318.8","gene_symbol":"ID3","gene_name":"inhibitor of DNA binding 3, HLH protein [Source:HGNC Symbol;Acc:HGNC:5362]","synonyms":"HEIR-1,bHLHb25","biotype":"protein_coding","ncbi_id":"3399","summary":"The protein encoded by this gene is a helix-loop-helix (HLH) protein that can form heterodimers with other HLH proteins. However, the encoded protein lacks a basic DNA-binding domain and therefore inhibits the DNA binding of any HLH protein with which it interacts. [provided by RefSeq, Aug 2011]","start":23557918,"end":23559794,"strand":-1,"description":"inhibitor of DNA binding 3, HLH protein [Source:HGNC Symbol;Acc:HGNC:5362]"}, {"versioned_ensembl_gene_id":"ENSG00000272804.3","gene_symbol":"KRTAP10-7","gene_name":"keratin associated protein 10-7 [Source:HGNC Symbol;Acc:HGNC:22970]","synonyms":"KRTAP18-7,KAP18.7,KAP10.7","biotype":"protein_coding","ncbi_id":"386675","summary":null,"start":44600597,"end":44602174,"strand":1,"description":"keratin associated protein 10-7 [Source:HGNC Symbol;Acc:HGNC:22970]"}, {"versioned_ensembl_gene_id":"ENSG00000188155.11","gene_symbol":"KRTAP10-6","gene_name":"keratin associated protein 10-6 [Source:HGNC Symbol;Acc:HGNC:20523]","synonyms":"KAP10.6,KRTAP18.6,KRTAP18-6,KAP18.6","biotype":"protein_coding","ncbi_id":"386674","summary":null,"start":44591268,"end":44592505,"strand":-1,"description":"keratin associated protein 10-6 [Source:HGNC Symbol;Acc:HGNC:20523]"}, {"versioned_ensembl_gene_id":"ENSG00000182912.6","gene_symbol":"TSPEAR-AS2","gene_name":"TSPEAR antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16428]","synonyms":"C21orf90","biotype":"antisense_RNA","ncbi_id":"114043","summary":null,"start":44517216,"end":44525952,"strand":1,"description":"TSPEAR antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16428]"}, {"versioned_ensembl_gene_id":"ENSG00000135686.12","gene_symbol":"KLHL36","gene_name":"kelch like family member 36 [Source:HGNC Symbol;Acc:HGNC:17844]","synonyms":"FLJ12543,C16orf44","biotype":"protein_coding","ncbi_id":"79786","summary":null,"start":84648525,"end":84667686,"strand":1,"description":"kelch like family member 36 [Source:HGNC Symbol;Acc:HGNC:17844]"}, {"versioned_ensembl_gene_id":"ENSG00000159496.14","gene_symbol":"RGL4","gene_name":"ral guanine nucleotide dissociation stimulator like 4 [Source:HGNC Symbol;Acc:HGNC:31911]","synonyms":"Rgr","biotype":"protein_coding","ncbi_id":"266747","summary":"This oncogene encodes a protein similar to guanine nucleotide exchange factor Ral guanine dissociation stimulator. Increased expression of this gene leads to translocation of the encoded protein to the cell membrane. The encoded protein can activate several pathways, including the Ras-Raf-MEK-ERK cascade. [provided by RefSeq, Jul 2016]","start":23688136,"end":23699176,"strand":1,"description":"ral guanine nucleotide dissociation stimulator like 4 [Source:HGNC Symbol;Acc:HGNC:31911]"}, {"versioned_ensembl_gene_id":"ENSG00000219867.1","gene_symbol":"AL590635.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":91815843,"end":91816428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187175.5","gene_symbol":"KRTAP12-1","gene_name":"keratin associated protein 12-1 [Source:HGNC Symbol;Acc:HGNC:20529]","synonyms":"KRTAP12.1,KAP12.1","biotype":"protein_coding","ncbi_id":"353332","summary":null,"start":44681576,"end":44682163,"strand":-1,"description":"keratin associated protein 12-1 [Source:HGNC Symbol;Acc:HGNC:20529]"}, {"versioned_ensembl_gene_id":"ENSG00000145604.15","gene_symbol":"SKP2","gene_name":"S-phase kinase associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10901]","synonyms":"p45,FBXL1,FBL1","biotype":"protein_coding","ncbi_id":"6502","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class; in addition to an F-box, this protein contains 10 tandem leucine-rich repeats. This protein is an essential element of the cyclin A-CDK2 S-phase kinase. It specifically recognizes phosphorylated cyclin-dependent kinase inhibitor 1B (CDKN1B, also referred to as p27 or KIP1) predominantly in S phase and interacts with S-phase kinase-associated protein 1 (SKP1 or p19). In addition, this gene is established as a protooncogene causally involved in the pathogenesis of lymphomas. Alternative splicing of this gene generates three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2011]","start":36151989,"end":36184319,"strand":1,"description":"S-phase kinase associated protein 2 [Source:HGNC Symbol;Acc:HGNC:10901]"}, {"versioned_ensembl_gene_id":"ENSG00000221963.5","gene_symbol":"APOL6","gene_name":"apolipoprotein L6 [Source:HGNC Symbol;Acc:HGNC:14870]","synonyms":"APOL-VI,APOLVI","biotype":"protein_coding","ncbi_id":"80830","summary":"This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. [provided by RefSeq, Jul 2008]","start":35648395,"end":35668409,"strand":1,"description":"apolipoprotein L6 [Source:HGNC Symbol;Acc:HGNC:14870]"}, {"versioned_ensembl_gene_id":"ENSG00000189169.7","gene_symbol":"KRTAP10-12","gene_name":"keratin associated protein 10-12 [Source:HGNC Symbol;Acc:HGNC:20533]","synonyms":"KRTAP18.12,KRTAP18-12,KAP10.12","biotype":"protein_coding","ncbi_id":"386685","summary":null,"start":44697172,"end":44698044,"strand":1,"description":"keratin associated protein 10-12 [Source:HGNC Symbol;Acc:HGNC:20533]"}, {"versioned_ensembl_gene_id":"ENSG00000230022.1","gene_symbol":"FNTAP2","gene_name":"farnesyltransferase, CAAX box, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3784]","synonyms":"FNTAL2","biotype":"processed_pseudogene","ncbi_id":"2341","summary":null,"start":21530690,"end":21531323,"strand":1,"description":"farnesyltransferase, CAAX box, alpha pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3784]"}, {"versioned_ensembl_gene_id":"ENSG00000233071.3","gene_symbol":"RPSAP59","gene_name":"ribosomal protein SA pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:36957]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271148","summary":null,"start":103206010,"end":103206899,"strand":-1,"description":"ribosomal protein SA pseudogene 59 [Source:HGNC Symbol;Acc:HGNC:36957]"}, {"versioned_ensembl_gene_id":"ENSG00000253339.1","gene_symbol":"AC111149.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73358913,"end":73362788,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166930.6","gene_symbol":"MS4A5","gene_name":"membrane spanning 4-domains A5 [Source:HGNC Symbol;Acc:HGNC:13374]","synonyms":"CD20L2","biotype":"protein_coding","ncbi_id":"64232","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. Though this member is not expressed in hematopoietic cells specifically, it may be involved in signal transduction like many of its related family members. The gene encoding this protein is localized to 11q12, among a cluster of family members. [provided by RefSeq, Jul 2008]","start":60429589,"end":60455214,"strand":1,"description":"membrane spanning 4-domains A5 [Source:HGNC Symbol;Acc:HGNC:13374]"}, {"versioned_ensembl_gene_id":"ENSG00000250764.1","gene_symbol":"AC025178.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32103445,"end":32121941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205445.3","gene_symbol":"KRTAP10-2","gene_name":"keratin associated protein 10-2 [Source:HGNC Symbol;Acc:HGNC:22967]","synonyms":"KRTAP18-2,KAP18.2,KAP10.2","biotype":"protein_coding","ncbi_id":"386679","summary":"This gene encodes a member of the high sulfur-type keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. This gene is located in a cluster of similar genes on 21q22.3. Alternatively-spliced transcript variants have been identified. [provided by RefSeq, Jan 2015]","start":44550357,"end":44551505,"strand":-1,"description":"keratin associated protein 10-2 [Source:HGNC Symbol;Acc:HGNC:22967]"}, {"versioned_ensembl_gene_id":"ENSG00000224971.1","gene_symbol":"SUMO2P3","gene_name":"SUMO2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652489","summary":null,"start":55732144,"end":55732431,"strand":1,"description":"SUMO2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39013]"}, {"versioned_ensembl_gene_id":"ENSG00000102409.9","gene_symbol":"BEX4","gene_name":"brain expressed X-linked 4 [Source:HGNC Symbol;Acc:HGNC:25475]","synonyms":"FLJ10097,BEXL1","biotype":"protein_coding","ncbi_id":"56271","summary":"This gene is a member of the brain expressed X-linked gene family. The proteins encoded by some of the other members of this family act as transcription elongation factors which allow RNA polymerase II to escape pausing during elongation. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2011]","start":103215092,"end":103217246,"strand":1,"description":"brain expressed X-linked 4 [Source:HGNC Symbol;Acc:HGNC:25475]"}, {"versioned_ensembl_gene_id":"ENSG00000205439.10","gene_symbol":"KRTAP12-3","gene_name":"keratin associated protein 12-3 [Source:HGNC Symbol;Acc:HGNC:20531]","synonyms":"KRTAP12.3","biotype":"protein_coding","ncbi_id":"386683","summary":null,"start":44657932,"end":44658341,"strand":1,"description":"keratin associated protein 12-3 [Source:HGNC Symbol;Acc:HGNC:20531]"}, {"versioned_ensembl_gene_id":"ENSG00000212935.1","gene_symbol":"KRTAP10-3","gene_name":"keratin associated protein 10-3 [Source:HGNC Symbol;Acc:HGNC:22968]","synonyms":"KRTAP18-3,KAP18.3,KAP10.3","biotype":"protein_coding","ncbi_id":"386682","summary":"This gene encodes a member of the keratin-associated protein (KAP) family. The KAP proteins form a matrix of keratin intermediate filaments which contribute to the structure of hair fibers. KAP family members appear to have unique, family-specific amino- and carboxyl-terminal regions and are subdivided into three multi-gene families according to amino acid composition: the high sulfur, the ultrahigh sulfur, and the high tyrosine/glycine KAPs. This gene encodes a member of the high sulfur KAP family. It is localized to a cluster of intronless KAPs at 21q22.3 which are located within the introns of the C21orf29 gene. [provided by RefSeq, Jul 2008]","start":44557790,"end":44558760,"strand":-1,"description":"keratin associated protein 10-3 [Source:HGNC Symbol;Acc:HGNC:22968]"}, {"versioned_ensembl_gene_id":"ENSG00000162073.13","gene_symbol":"PAQR4","gene_name":"progestin and adipoQ receptor family member 4 [Source:HGNC Symbol;Acc:HGNC:26386]","synonyms":"FLJ30002","biotype":"protein_coding","ncbi_id":"124222","summary":null,"start":2969245,"end":2973489,"strand":1,"description":"progestin and adipoQ receptor family member 4 [Source:HGNC Symbol;Acc:HGNC:26386]"}, {"versioned_ensembl_gene_id":"ENSG00000230254.7","gene_symbol":"HLA-E","gene_name":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3133","summary":"HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":30481701,"end":30486439,"strand":1,"description":"major histocompatibility complex, class I, E [Source:HGNC Symbol;Acc:HGNC:4962]"}, {"versioned_ensembl_gene_id":"ENSG00000187766.1","gene_symbol":"KRTAP10-8","gene_name":"keratin associated protein 10-8 [Source:HGNC Symbol;Acc:HGNC:20525]","synonyms":"KRTAP18.8,KRTAP18-8,KAP10.8","biotype":"protein_coding","ncbi_id":"386681","summary":null,"start":44612079,"end":44612954,"strand":1,"description":"keratin associated protein 10-8 [Source:HGNC Symbol;Acc:HGNC:20525]"}, {"versioned_ensembl_gene_id":"ENSG00000236382.1","gene_symbol":"KRTAP10-13P","gene_name":"keratin associated protein 10-13, pseudogene [Source:HGNC Symbol;Acc:HGNC:34213]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100874224","summary":null,"start":44702221,"end":44702791,"strand":1,"description":"keratin associated protein 10-13, pseudogene [Source:HGNC Symbol;Acc:HGNC:34213]"}, {"versioned_ensembl_gene_id":"ENSG00000150681.9","gene_symbol":"RGS18","gene_name":"regulator of G protein signaling 18 [Source:HGNC Symbol;Acc:HGNC:14261]","synonyms":"RGS13","biotype":"protein_coding","ncbi_id":"64407","summary":"This gene encodes a member of the regulator of G-protein signaling family. This protein is contains a conserved, 120 amino acid motif called the RGS domain. The protein attenuates the signaling activity of G-proteins by binding to activated, GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]","start":192158457,"end":192185815,"strand":1,"description":"regulator of G protein signaling 18 [Source:HGNC Symbol;Acc:HGNC:14261]"}, {"versioned_ensembl_gene_id":"ENSG00000273174.1","gene_symbol":"AC108673.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":129123439,"end":129124003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221859.2","gene_symbol":"KRTAP10-10","gene_name":"keratin associated protein 10-10 [Source:HGNC Symbol;Acc:HGNC:22972]","synonyms":"KRTAP18-10,KAP18.10,KAP10.10","biotype":"protein_coding","ncbi_id":"353333","summary":null,"start":44637356,"end":44638455,"strand":1,"description":"keratin associated protein 10-10 [Source:HGNC Symbol;Acc:HGNC:22972]"}, {"versioned_ensembl_gene_id":"ENSG00000275681.1","gene_symbol":"U73479.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21841794,"end":21841961,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147533.16","gene_symbol":"GOLGA7","gene_name":"golgin A7 [Source:HGNC Symbol;Acc:HGNC:24876]","synonyms":"HSPC041,GOLGA7A,GOLGA3AP1,GCP16","biotype":"protein_coding","ncbi_id":"51125","summary":null,"start":41490396,"end":41510980,"strand":1,"description":"golgin A7 [Source:HGNC Symbol;Acc:HGNC:24876]"}, {"versioned_ensembl_gene_id":"ENSG00000228837.2","gene_symbol":"CBX3P6","gene_name":"chromobox 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42878]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642721","summary":null,"start":154940541,"end":154941067,"strand":-1,"description":"chromobox 3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42878]"}, {"versioned_ensembl_gene_id":"ENSG00000280164.1","gene_symbol":"CU638689.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6721812,"end":6725209,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230991.1","gene_symbol":"AC092625.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":154965513,"end":154968003,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261365.1","gene_symbol":"AC138749.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28473322,"end":28473448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104687.12","gene_symbol":"GSR","gene_name":"glutathione-disulfide reductase [Source:HGNC Symbol;Acc:HGNC:4623]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2936","summary":"This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. This enzyme is a homodimeric flavoprotein. It is a central enzyme of cellular antioxidant defense, and reduces oxidized glutathione disulfide (GSSG) to the sulfhydryl form GSH, which is an important cellular antioxidant. Rare mutations in this gene result in hereditary glutathione reductase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Aug 2010]","start":30678061,"end":30727926,"strand":-1,"description":"glutathione-disulfide reductase [Source:HGNC Symbol;Acc:HGNC:4623]"}, {"versioned_ensembl_gene_id":"ENSG00000233359.1","gene_symbol":"AC114485.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102199739,"end":102389630,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279998.1","gene_symbol":"FP475955.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6789592,"end":6812297,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218428.1","gene_symbol":"NIP7P3","gene_name":"NIP7, nucleolar pre-rRNA processing protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45182]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421245","summary":null,"start":116137058,"end":116137572,"strand":-1,"description":"NIP7, nucleolar pre-rRNA processing protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45182]"}, {"versioned_ensembl_gene_id":"ENSG00000232982.1","gene_symbol":"MTCO1P45","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52110]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075174","summary":null,"start":155263458,"end":155263724,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:52110]"}, {"versioned_ensembl_gene_id":"ENSG00000236326.1","gene_symbol":"AL050331.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116244187,"end":116244728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182272.11","gene_symbol":"B4GALNT4","gene_name":"beta-1,4-N-acetyl-galactosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:26315]","synonyms":"NGalNAc-T1,FLJ25045","biotype":"protein_coding","ncbi_id":"338707","summary":null,"start":369796,"end":382116,"strand":1,"description":"beta-1,4-N-acetyl-galactosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:26315]"}, {"versioned_ensembl_gene_id":"ENSG00000178425.13","gene_symbol":"NT5DC1","gene_name":"5'-nucleotidase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21556]","synonyms":"NT5C2L1,MGC24302,dJ486I3.1","biotype":"protein_coding","ncbi_id":"221294","summary":"While the exact function of the protein encoded by this gene is not known, it belongs to the 5'(3')-deoxyribonucleotidase family. [provided by RefSeq, May 2010]","start":116100849,"end":116249497,"strand":1,"description":"5'-nucleotidase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:21556]"}, {"versioned_ensembl_gene_id":"ENSG00000274814.1","gene_symbol":"AC138749.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28494975,"end":28495182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226279.2","gene_symbol":"RPL12P10","gene_name":"ribosomal protein L12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:22583]","synonyms":"TCAG_1783340","biotype":"processed_pseudogene","ncbi_id":"392872","summary":null,"start":22881893,"end":22882390,"strand":1,"description":"ribosomal protein L12 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:22583]"}, {"versioned_ensembl_gene_id":"ENSG00000168300.13","gene_symbol":"PCMTD1","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30483]","synonyms":"FLJ10883","biotype":"protein_coding","ncbi_id":"115294","summary":null,"start":51817575,"end":51899186,"strand":-1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:30483]"}, {"versioned_ensembl_gene_id":"ENSG00000278955.3","gene_symbol":"FP475955.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6858539,"end":6897263,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260053.2","gene_symbol":"ABCB10P4","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132289","summary":null,"start":28506625,"end":28508808,"strand":-1,"description":"ATP binding cassette subfamily B member 10 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31130]"}, {"versioned_ensembl_gene_id":"ENSG00000280172.1","gene_symbol":"FP475955.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6897291,"end":6899280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232672.1","gene_symbol":"ACTG1P21","gene_name":"actin gamma 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51501]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131291","summary":null,"start":77773865,"end":77774864,"strand":-1,"description":"actin gamma 1 pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:51501]"}, {"versioned_ensembl_gene_id":"ENSG00000279751.1","gene_symbol":"FP475955.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6904884,"end":6906692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235107.3","gene_symbol":"RING1","gene_name":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]","synonyms":"RNF1","biotype":"protein_coding","ncbi_id":"6015","summary":"This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]","start":33362379,"end":33366606,"strand":1,"description":"ring finger protein 1 [Source:HGNC Symbol;Acc:HGNC:10018]"}, {"versioned_ensembl_gene_id":"ENSG00000281248.1","gene_symbol":"LINC02536","gene_name":"long intergenic non-protein coding RNA 2536 [Source:HGNC Symbol;Acc:HGNC:53570]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377997","summary":null,"start":127664554,"end":127681555,"strand":1,"description":"long intergenic non-protein coding RNA 2536 [Source:HGNC Symbol;Acc:HGNC:53570]"}, {"versioned_ensembl_gene_id":"ENSG00000127564.16","gene_symbol":"PKMYT1","gene_name":"protein kinase, membrane associated tyrosine/threonine 1 [Source:HGNC Symbol;Acc:HGNC:29650]","synonyms":"PPP1R126,MYT1","biotype":"protein_coding","ncbi_id":"9088","summary":"This gene encodes a member of the serine/threonine protein kinase family. The encoded protein is a membrane-associated kinase that negatively regulates the G2/M transition of the cell cycle by phosphorylating and inactivating cyclin-dependent kinase 1. The activity of the encoded protein is regulated by polo-like kinase 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]","start":2968024,"end":2980539,"strand":-1,"description":"protein kinase, membrane associated tyrosine/threonine 1 [Source:HGNC Symbol;Acc:HGNC:29650]"}, {"versioned_ensembl_gene_id":"ENSG00000231660.1","gene_symbol":"RPS8P6","gene_name":"ribosomal protein S8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36947]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270871","summary":null,"start":308714,"end":309322,"strand":-1,"description":"ribosomal protein S8 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:36947]"}, {"versioned_ensembl_gene_id":"ENSG00000189308.10","gene_symbol":"LIN54","gene_name":"lin-54 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:25397]","synonyms":"TCX1,MIP120,JC8.6,DKFZp686L1814,CXCDC1","biotype":"protein_coding","ncbi_id":"132660","summary":"LIN54 is a component of the LIN, or DREAM, complex, an essential regulator of cell cycle genes (Schmit et al., 2009 [PubMed 19725879]).[supplied by OMIM, Dec 2010]","start":82909973,"end":83012926,"strand":-1,"description":"lin-54 DREAM MuvB core complex component [Source:HGNC Symbol;Acc:HGNC:25397]"}, {"versioned_ensembl_gene_id":"ENSG00000013374.15","gene_symbol":"NUB1","gene_name":"negative regulator of ubiquitin like proteins 1 [Source:HGNC Symbol;Acc:HGNC:17623]","synonyms":"NYREN18,NUB1L,BS4","biotype":"protein_coding","ncbi_id":"51667","summary":"This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":151341699,"end":151378449,"strand":1,"description":"negative regulator of ubiquitin like proteins 1 [Source:HGNC Symbol;Acc:HGNC:17623]"}, {"versioned_ensembl_gene_id":"ENSG00000117600.12","gene_symbol":"PLPPR4","gene_name":"phospholipid phosphatase related 4 [Source:HGNC Symbol;Acc:HGNC:23496]","synonyms":"PRG-1,PHP1,LPPR4,KIAA0455","biotype":"protein_coding","ncbi_id":"9890","summary":"The protein encoded by this gene belongs to the lipid phosphate phosphatase (LPP) family. LPPs catalyze the dephosphorylation of a number of bioactive lipid mediators that regulate a variety of cell functions. This protein is specifically expressed in neurons. It is located in the membranes of outgrowing axons and has been shown to be important for axonal outgrowth during development and regenerative sprouting. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]","start":99263953,"end":99309590,"strand":1,"description":"phospholipid phosphatase related 4 [Source:HGNC Symbol;Acc:HGNC:23496]"}, {"versioned_ensembl_gene_id":"ENSG00000140986.7","gene_symbol":"RPL3L","gene_name":"ribosomal protein L3 like [Source:HGNC Symbol;Acc:HGNC:10351]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6123","summary":"This gene encodes a protein that shares sequence similarity with ribosomal protein L3. The protein belongs to the L3P family of ribosomal proteins. Unlike the ubiquitous expression of ribosomal protein genes, this gene has a tissue-specific pattern of expression, with the highest levels of expression in skeletal muscle and heart. It is not currently known whether the encoded protein is a functional ribosomal protein or whether it has evolved a function that is independent of the ribosome. [provided by RefSeq, Jul 2008]","start":1943974,"end":1957606,"strand":-1,"description":"ribosomal protein L3 like [Source:HGNC Symbol;Acc:HGNC:10351]"}, {"versioned_ensembl_gene_id":"ENSG00000278788.4","gene_symbol":"SBNO2","gene_name":"strawberry notch homolog 2 [Source:HGNC Symbol;Acc:HGNC:29158]","synonyms":"FLJ00173,Stno,Sno,KIAA0963","biotype":"protein_coding","ncbi_id":"22904","summary":null,"start":1107635,"end":1156979,"strand":-1,"description":"strawberry notch homolog 2 [Source:HGNC Symbol;Acc:HGNC:29158]"}, {"versioned_ensembl_gene_id":"ENSG00000249114.1","gene_symbol":"AC022447.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31738269,"end":31738660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224282.3","gene_symbol":"AC010469.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31822561,"end":31823136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255568.3","gene_symbol":"BRWD1-AS2","gene_name":"BRWD1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16423]","synonyms":"C21orf87,BRWD1-IT2,NCRNA00257","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39313935,"end":39314962,"strand":1,"description":"BRWD1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:16423]"}, {"versioned_ensembl_gene_id":"ENSG00000249774.1","gene_symbol":"AC025458.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31923367,"end":31923532,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250164.1","gene_symbol":"AC022447.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31747644,"end":31748078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203413.3","gene_symbol":"ACTBP6","gene_name":"actin, beta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:139]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"66","summary":null,"start":84948585,"end":84949674,"strand":1,"description":"actin, beta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:139]"}, {"versioned_ensembl_gene_id":"ENSG00000248624.1","gene_symbol":"AC022447.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31657218,"end":31665067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237373.1","gene_symbol":"BRWD1-IT1","gene_name":"BRWD1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41920]","synonyms":null,"biotype":"sense_overlapping","ncbi_id":"106480743","summary":null,"start":39217093,"end":39219805,"strand":-1,"description":"BRWD1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41920]"}, {"versioned_ensembl_gene_id":"ENSG00000163606.10","gene_symbol":"CD200R1","gene_name":"CD200 receptor 1 [Source:HGNC Symbol;Acc:HGNC:24235]","synonyms":"MOX2R,HCRTR2,CD200R,OX2R","biotype":"protein_coding","ncbi_id":"131450","summary":"This gene encodes a receptor for the OX-2 membrane glycoprotein. Both the receptor and substrate are cell surface glycoproteins containing two immunoglobulin-like domains. This receptor is restricted to the surfaces of myeloid lineage cells and the receptor-substrate interaction may function as a myeloid downregulatory signal. Mouse studies of a related gene suggest that this interaction may control myeloid function in a tissue-specific manner. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008]","start":112921209,"end":112975122,"strand":-1,"description":"CD200 receptor 1 [Source:HGNC Symbol;Acc:HGNC:24235]"}, {"versioned_ensembl_gene_id":"ENSG00000253655.2","gene_symbol":"IGJP1","gene_name":"immunoglobulin J polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5714]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"3513","summary":null,"start":84980073,"end":84980547,"strand":-1,"description":"immunoglobulin J polypeptide pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5714]"}, {"versioned_ensembl_gene_id":"ENSG00000256331.1","gene_symbol":"NIFKP3","gene_name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44951]","synonyms":"MKI67IPP3","biotype":"processed_pseudogene","ncbi_id":"100270648","summary":null,"start":7604350,"end":7605214,"strand":-1,"description":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44951]"}, {"versioned_ensembl_gene_id":"ENSG00000248378.1","gene_symbol":"AC022447.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31743988,"end":31744451,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270767.1","gene_symbol":"AL356157.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44488335,"end":44488445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214108.4","gene_symbol":"TPT1P5","gene_name":"tumor protein, translationally-controlled 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49296]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421420","summary":null,"start":31908361,"end":31909186,"strand":1,"description":"tumor protein, translationally-controlled 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49296]"}, {"versioned_ensembl_gene_id":"ENSG00000234580.1","gene_symbol":"AL356157.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44591208,"end":44602104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255977.1","gene_symbol":"AC006927.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7606834,"end":7607331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233451.1","gene_symbol":"AL513128.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":22361172,"end":22413067,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243914.1","gene_symbol":"RPL5P14","gene_name":"ribosomal protein L5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270835","summary":null,"start":31847271,"end":31848148,"strand":1,"description":"ribosomal protein L5 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:35924]"}, {"versioned_ensembl_gene_id":"ENSG00000227395.1","gene_symbol":"EIF2AP4","gene_name":"eukaryotic translation initiation factor 2A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39498]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874401","summary":null,"start":44806443,"end":44808223,"strand":1,"description":"eukaryotic translation initiation factor 2A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39498]"}, {"versioned_ensembl_gene_id":"ENSG00000249688.1","gene_symbol":"AC022447.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31754219,"end":31754656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284327.1","gene_symbol":"AC006927.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7619872,"end":7620260,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253475.1","gene_symbol":"AC103769.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":51895957,"end":51896374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123500.9","gene_symbol":"COL10A1","gene_name":"collagen type X alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2185]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1300","summary":"This gene encodes the alpha chain of type X collagen, a short chain collagen expressed by hypertrophic chondrocytes during endochondral ossification. Unlike type VIII collagen, the other short chain collagen, type X collagen is a homotrimer. Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD). [provided by RefSeq, Jul 2008]","start":116118923,"end":116158747,"strand":-1,"description":"collagen type X alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2185]"}, {"versioned_ensembl_gene_id":"ENSG00000282924.1","gene_symbol":"AC136428.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33723356,"end":33763773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133401.15","gene_symbol":"PDZD2","gene_name":"PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18486]","synonyms":"PDZK3,KIAA0300","biotype":"protein_coding","ncbi_id":"23037","summary":"The protein encoded by this gene contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, this gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis. [provided by RefSeq, Dec 2015]","start":31639410,"end":32110931,"strand":1,"description":"PDZ domain containing 2 [Source:HGNC Symbol;Acc:HGNC:18486]"}, {"versioned_ensembl_gene_id":"ENSG00000226491.1","gene_symbol":"FTOP1","gene_name":"fat mass and obesity associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43759]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874223","summary":null,"start":42797225,"end":42798712,"strand":-1,"description":"fat mass and obesity associated pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43759]"}, {"versioned_ensembl_gene_id":"ENSG00000141506.13","gene_symbol":"PIK3R5","gene_name":"phosphoinositide-3-kinase regulatory subunit 5 [Source:HGNC Symbol;Acc:HGNC:30035]","synonyms":"P101-PI3K,p101","biotype":"protein_coding","ncbi_id":"23533","summary":"Phosphatidylinositol 3-kinases (PI3Ks) phosphorylate the inositol ring of phosphatidylinositol at the 3-prime position, and play important roles in cell growth, proliferation, differentiation, motility, survival and intracellular trafficking. The PI3Ks are divided into three classes: I, II and III, and only the class I PI3Ks are involved in oncogenesis. This gene encodes the 101 kD regulatory subunit of the class I PI3K gamma complex, which is a dimeric enzyme, consisting of a 110 kD catalytic subunit gamma and a regulatory subunit of either 55, 87 or 101 kD. This protein recruits the catalytic subunit from the cytosol to the plasma membrane through high-affinity interaction with G-beta-gamma proteins. Multiple alternatively spliced transcript variants encoding two distinct isoforms have been found. [provided by RefSeq, Oct 2011]","start":8878911,"end":8965712,"strand":-1,"description":"phosphoinositide-3-kinase regulatory subunit 5 [Source:HGNC Symbol;Acc:HGNC:30035]"}, {"versioned_ensembl_gene_id":"ENSG00000284591.1","gene_symbol":"AC006927.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7620542,"end":7621450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232202.1","gene_symbol":"AC098824.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42826322,"end":42827617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155229.20","gene_symbol":"MMS19","gene_name":"MMS19 homolog, cytosolic iron-sulfur assembly component [Source:HGNC Symbol;Acc:HGNC:13824]","synonyms":"MMS19L,MET18,hMMS19","biotype":"protein_coding","ncbi_id":"64210","summary":null,"start":97458324,"end":97498794,"strand":-1,"description":"MMS19 homolog, cytosolic iron-sulfur assembly component [Source:HGNC Symbol;Acc:HGNC:13824]"}, {"versioned_ensembl_gene_id":"ENSG00000249405.1","gene_symbol":"AC022441.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50858760,"end":50860020,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206401.11","gene_symbol":"LY6G6E","gene_name":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]","synonyms":"C6orf22,G6e","biotype":"protein_coding","ncbi_id":"79136","summary":"LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31702563,"end":31704039,"strand":-1,"description":"lymphocyte antigen 6 family member G6E [Source:HGNC Symbol;Acc:HGNC:13934]"}, {"versioned_ensembl_gene_id":"ENSG00000131910.4","gene_symbol":"NR0B2","gene_name":"nuclear receptor subfamily 0 group B member 2 [Source:HGNC Symbol;Acc:HGNC:7961]","synonyms":"SHP","biotype":"protein_coding","ncbi_id":"8431","summary":"The protein encoded by this gene is an unusual orphan receptor that contains a putative ligand-binding domain but lacks a conventional DNA-binding domain. The gene product is a member of the nuclear hormone receptor family, a group of transcription factors regulated by small hydrophobic hormones, a subset of which do not have known ligands and are referred to as orphan nuclear receptors. The protein has been shown to interact with retinoid and thyroid hormone receptors, inhibiting their ligand-dependent transcriptional activation. In addition, interaction with estrogen receptors has been demonstrated, leading to inhibition of function. Studies suggest that the protein represses nuclear hormone receptor-mediated transactivation via two separate steps: competition with coactivators and the direct effects of its transcriptional repressor function. [provided by RefSeq, Jul 2008]","start":26911489,"end":26913966,"strand":-1,"description":"nuclear receptor subfamily 0 group B member 2 [Source:HGNC Symbol;Acc:HGNC:7961]"}, {"versioned_ensembl_gene_id":"ENSG00000159685.10","gene_symbol":"CHCHD6","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 6 [Source:HGNC Symbol;Acc:HGNC:28184]","synonyms":"PPP1R23,Mic25,MGC13016,CHCM1","biotype":"protein_coding","ncbi_id":"84303","summary":null,"start":126704220,"end":126960406,"strand":1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 6 [Source:HGNC Symbol;Acc:HGNC:28184]"}, {"versioned_ensembl_gene_id":"ENSG00000211683.3","gene_symbol":"AP000346.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23630618,"end":23638941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224220.1","gene_symbol":"AC104699.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":25421117,"end":25427643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162738.5","gene_symbol":"VANGL2","gene_name":"VANGL planar cell polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:15511]","synonyms":"STBM1,STBM,STB1,MGC119404,MGC119403,LTAP,LPP1,KIAA1215","biotype":"protein_coding","ncbi_id":"57216","summary":"The protein encoded by this gene is a membrane protein involved in the regulation of planar cell polarity, especially in the stereociliary bundles of the cochlea. The encoded protein transmits directional signals to individual cells or groups of cells in epithelial sheets. This protein is also involved in the development of the neural plate. [provided by RefSeq, Sep 2011]","start":160400586,"end":160428678,"strand":1,"description":"VANGL planar cell polarity protein 2 [Source:HGNC Symbol;Acc:HGNC:15511]"}, {"versioned_ensembl_gene_id":"ENSG00000243804.1","gene_symbol":"LY6G6F","gene_name":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]","synonyms":"C6orf21,LY6G6D,G6f,NG32","biotype":"protein_coding","ncbi_id":"259215","summary":"The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]","start":31697109,"end":31700820,"strand":1,"description":"lymphocyte antigen 6 family member G6F [Source:HGNC Symbol;Acc:HGNC:13933]"}, {"versioned_ensembl_gene_id":"ENSG00000230955.1","gene_symbol":"AL929472.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37860697,"end":37861580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228785.1","gene_symbol":"HLA-Z","gene_name":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]","synonyms":"HLA-Z1","biotype":"unprocessed_pseudogene","ncbi_id":"267017","summary":null,"start":32818730,"end":32818804,"strand":1,"description":"major histocompatibility complex, class I, Z (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19394]"}, {"versioned_ensembl_gene_id":"ENSG00000273000.5","gene_symbol":"AP000347.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23652860,"end":23717347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090273.13","gene_symbol":"NUDC","gene_name":"nuclear distribution C, dynein complex regulator [Source:HGNC Symbol;Acc:HGNC:8045]","synonyms":"NudC","biotype":"protein_coding","ncbi_id":"10726","summary":"This gene encodes a nuclear distribution protein that plays an essential role in mitosis and cytokinesis. The encoded protein is involved in spindle formation during mitosis and in microtubule organization during cytokinesis. Pseudogenes of this gene are found on chromosome 2. [provided by RefSeq, Feb 2012]","start":26900238,"end":26946862,"strand":1,"description":"nuclear distribution C, dynein complex regulator [Source:HGNC Symbol;Acc:HGNC:8045]"}, {"versioned_ensembl_gene_id":"ENSG00000230828.1","gene_symbol":"AL583843.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50114937,"end":50115282,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251601.1","gene_symbol":"AC022441.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50929484,"end":50934521,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204084.12","gene_symbol":"INPP5B","gene_name":"inositol polyphosphate-5-phosphatase B [Source:HGNC Symbol;Acc:HGNC:6077]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3633","summary":"This gene encodes a member of a family of inositol polyphosphate-5-phosphatases. These enzymes function in the regulation of calcium signaling by inactivating inositol phosphates. The encoded protein is localized to the cytosol and mitochondria, and associates with membranes through an isoprenyl modification near the C-terminus. Alternatively spliced transcript variants of this gene have been described. [provided by RefSeq, Jul 2014]","start":37860697,"end":37947057,"strand":-1,"description":"inositol polyphosphate-5-phosphatase B [Source:HGNC Symbol;Acc:HGNC:6077]"}, {"versioned_ensembl_gene_id":"ENSG00000162374.16","gene_symbol":"ELAVL4","gene_name":"ELAV like RNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3315]","synonyms":"PNEM,HUD","biotype":"protein_coding","ncbi_id":"1996","summary":null,"start":50048014,"end":50203786,"strand":1,"description":"ELAV like RNA binding protein 4 [Source:HGNC Symbol;Acc:HGNC:3315]"}, {"versioned_ensembl_gene_id":"ENSG00000250360.1","gene_symbol":"AC008808.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50965687,"end":50967008,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138101.18","gene_symbol":"DTNB","gene_name":"dystrobrevin beta [Source:HGNC Symbol;Acc:HGNC:3058]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1838","summary":"This gene encodes dystrobrevin beta, a component of the dystrophin-associated protein complex (DPC). The DPC consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and dystrobrevin alpha and beta. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Dystrobrevin beta is thought to interact with syntrophin and the DP71 short form of dystrophin. [provided by RefSeq, Mar 2016]","start":25377198,"end":25673647,"strand":-1,"description":"dystrobrevin beta [Source:HGNC Symbol;Acc:HGNC:3058]"}, {"versioned_ensembl_gene_id":"ENSG00000127993.15","gene_symbol":"RBM48","gene_name":"RNA binding motif protein 48 [Source:HGNC Symbol;Acc:HGNC:21785]","synonyms":"C7orf64,HSPC304,DKFZp564O0523","biotype":"protein_coding","ncbi_id":"84060","summary":null,"start":92528773,"end":92538005,"strand":1,"description":"RNA binding motif protein 48 [Source:HGNC Symbol;Acc:HGNC:21785]"}, {"versioned_ensembl_gene_id":"ENSG00000237748.1","gene_symbol":"UQCRBP1","gene_name":"ubiquinol-cytochrome c reductase binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12583]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442454","summary":null,"start":56737242,"end":56737577,"strand":-1,"description":"ubiquinol-cytochrome c reductase binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:12583]"}, {"versioned_ensembl_gene_id":"ENSG00000251573.2","gene_symbol":"LINC02106","gene_name":"long intergenic non-protein coding RNA 2106 [Source:HGNC Symbol;Acc:HGNC:52961]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100287592","summary":null,"start":50969217,"end":50970167,"strand":-1,"description":"long intergenic non-protein coding RNA 2106 [Source:HGNC Symbol;Acc:HGNC:52961]"}, {"versioned_ensembl_gene_id":"ENSG00000275609.1","gene_symbol":"AP000346.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23610329,"end":23610538,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224799.1","gene_symbol":"AL139397.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56973510,"end":56974796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183091.19","gene_symbol":"NEB","gene_name":"nebulin [Source:HGNC Symbol;Acc:HGNC:7720]","synonyms":"NEM2,NEB177D","biotype":"protein_coding","ncbi_id":"4703","summary":"This gene encodes nebulin, a giant protein component of the cytoskeletal matrix that coexists with the thick and thin filaments within the sarcomeres of skeletal muscle. In most vertebrates, nebulin accounts for 3 to 4% of the total myofibrillar protein. The encoded protein contains approximately 30-amino acid long modules that can be classified into 7 types and other repeated modules. Protein isoform sizes vary from 600 to 800 kD due to alternative splicing that is tissue-, species-,and developmental stage-specific. Of the 183 exons in the nebulin gene, at least 43 are alternatively spliced, although exons 143 and 144 are not found in the same transcript. Of the several thousand transcript variants predicted for nebulin, the RefSeq Project has decided to create three representative RefSeq records. Mutations in this gene are associated with recessive nemaline myopathy. [provided by RefSeq, Sep 2009]","start":151485336,"end":151734487,"strand":-1,"description":"nebulin [Source:HGNC Symbol;Acc:HGNC:7720]"}, {"versioned_ensembl_gene_id":"ENSG00000272578.5","gene_symbol":"AP000347.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23658094,"end":23717356,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206402.10","gene_symbol":"LY6G6D","gene_name":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]","synonyms":"G6D,MEGT1,C6orf23,Ly6-D,NG25","biotype":"protein_coding","ncbi_id":"58530","summary":"LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]","start":31697128,"end":31708139,"strand":1,"description":"lymphocyte antigen 6 family member G6D [Source:HGNC Symbol;Acc:HGNC:13935]"}, {"versioned_ensembl_gene_id":"ENSG00000187783.11","gene_symbol":"TMEM72","gene_name":"transmembrane protein 72 [Source:HGNC Symbol;Acc:HGNC:31658]","synonyms":"KSP37,C10orf127,bA285G1.3","biotype":"protein_coding","ncbi_id":"643236","summary":"This gene encodes a transmembrane protein which may be expressed specifically in the kidney. [provided by RefSeq, Sep 2016]","start":44911200,"end":44937002,"strand":1,"description":"transmembrane protein 72 [Source:HGNC Symbol;Acc:HGNC:31658]"}, {"versioned_ensembl_gene_id":"ENSG00000168081.8","gene_symbol":"PNOC","gene_name":"prepronociceptin [Source:HGNC Symbol;Acc:HGNC:9163]","synonyms":"PPNOC,NOP,N/OFQ","biotype":"protein_coding","ncbi_id":"5368","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include nociceptin, nocistatin, and orphanin FQ2 (OFQ2). Nociceptin, also known as orphanin FQ, is a 17-amino acid neuropeptide that binds to the nociceptin receptor to induce increased pain sensitivity, and may additionally regulate body temperature, learning and memory, and hunger. Another product of the encoded preproprotein, nocistatin, may inhibit the effects of nociceptin. [provided by RefSeq, Jul 2015]","start":28316986,"end":28343355,"strand":1,"description":"prepronociceptin [Source:HGNC Symbol;Acc:HGNC:9163]"}, {"versioned_ensembl_gene_id":"ENSG00000278734.1","gene_symbol":"AC091834.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51101172,"end":51101643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156650.12","gene_symbol":"KAT6B","gene_name":"lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]","synonyms":"ZC2HC6B,querkopf,qkf,MYST4,MOZ2,Morf","biotype":"protein_coding","ncbi_id":"23522","summary":"The protein encoded by this gene is a histone acetyltransferase and component of the MOZ/MORF protein complex. In addition to its acetyltransferase activity, the encoded protein has transcriptional activation activity in its N-terminal end and transcriptional repression activity in its C-terminal end. This protein is necessary for RUNX2-dependent transcriptional activation and could be involved in brain development. Mutations have been found in patients with genitopatellar syndrome. A translocation of this gene and the CREBBP gene results in acute myeloid leukemias. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":74825582,"end":75032622,"strand":1,"description":"lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]"}, {"versioned_ensembl_gene_id":"ENSG00000100368.13","gene_symbol":"CSF2RB","gene_name":"colony stimulating factor 2 receptor beta common subunit [Source:HGNC Symbol;Acc:HGNC:2436]","synonyms":"CD131,IL5RB,IL3RB","biotype":"protein_coding","ncbi_id":"1439","summary":"The protein encoded by this gene is the common beta chain of the high affinity receptor for IL-3, IL-5 and CSF. Defects in this gene have been reported to be associated with protein alveolar proteinosis (PAP). [provided by RefSeq, Jul 2008]","start":36913628,"end":36940449,"strand":1,"description":"colony stimulating factor 2 receptor beta common subunit [Source:HGNC Symbol;Acc:HGNC:2436]"}, {"versioned_ensembl_gene_id":"ENSG00000155026.16","gene_symbol":"RSPH10B","gene_name":"radial spoke head 10 homolog B [Source:HGNC Symbol;Acc:HGNC:27362]","synonyms":null,"biotype":"protein_coding","ncbi_id":"222967","summary":null,"start":5925550,"end":5970683,"strand":-1,"description":"radial spoke head 10 homolog B [Source:HGNC Symbol;Acc:HGNC:27362]"}, {"versioned_ensembl_gene_id":"ENSG00000189241.6","gene_symbol":"TSPYL1","gene_name":"TSPY like 1 [Source:HGNC Symbol;Acc:HGNC:12382]","synonyms":"TSPYL","biotype":"protein_coding","ncbi_id":"7259","summary":"The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009]","start":116276578,"end":116279903,"strand":-1,"description":"TSPY like 1 [Source:HGNC Symbol;Acc:HGNC:12382]"}, {"versioned_ensembl_gene_id":"ENSG00000181404.15","gene_symbol":"WASHC1","gene_name":"WASH complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24361]","synonyms":"WASH1,FLJ00038,FAM39E","biotype":"protein_coding","ncbi_id":"100287171","summary":null,"start":14521,"end":29739,"strand":-1,"description":"WASH complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:24361]"}, {"versioned_ensembl_gene_id":"ENSG00000273211.1","gene_symbol":"AC137630.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48985485,"end":48985963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226713.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29960749,"end":29962411,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000235236.1","gene_symbol":"AC137630.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48979918,"end":48983985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228315.11","gene_symbol":"GUSBP11","gene_name":"glucuronidase, beta pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42325]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"91316","summary":"This transcribed pseudogene is similar to two functional genes. The 5' portion of the pseudogene is related to glucuronidase, beta, and the 3' portion is related to immunoglobulin lambda-like polypeptide 1. [provided by RefSeq, Jul 2011]","start":23638487,"end":23717356,"strand":-1,"description":"glucuronidase, beta pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:42325]"}, {"versioned_ensembl_gene_id":"ENSG00000227669.3","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29879367,"end":29882089,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000204421.2","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"G6c,C6orf24,NG24","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31718648,"end":31721845,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000165507.8","gene_symbol":"C10orf10","gene_name":"chromosome 10 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:23355]","synonyms":"Fseg,FIG,DEPP","biotype":"protein_coding","ncbi_id":"11067","summary":"The expression of this gene is induced by fasting as well as by progesterone. The protein encoded by this gene contains a t-synaptosome-associated protein receptor (SNARE) coiled-coil homology domain and a peroxisomal targeting signal. Production of the encoded protein leads to phosphorylation and activation of the transcription factor ELK1. [provided by RefSeq, Jul 2008]","start":44970981,"end":44978810,"strand":-1,"description":"chromosome 10 open reading frame 10 [Source:HGNC Symbol;Acc:HGNC:23355]"}, {"versioned_ensembl_gene_id":"ENSG00000234849.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29946543,"end":29948517,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000197880.8","gene_symbol":"MDS2","gene_name":"myelodysplastic syndrome 2 translocation associated [Source:HGNC Symbol;Acc:HGNC:29633]","synonyms":null,"biotype":"protein_coding","ncbi_id":"259283","summary":null,"start":23581495,"end":23640568,"strand":1,"description":"myelodysplastic syndrome 2 translocation associated [Source:HGNC Symbol;Acc:HGNC:29633]"}, {"versioned_ensembl_gene_id":"ENSG00000229243.1","gene_symbol":"LINC01981","gene_name":"long intergenic non-protein coding RNA 1981 [Source:HGNC Symbol;Acc:HGNC:52809]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996624","summary":null,"start":27830888,"end":27834136,"strand":-1,"description":"long intergenic non-protein coding RNA 1981 [Source:HGNC Symbol;Acc:HGNC:52809]"}, {"versioned_ensembl_gene_id":"ENSG00000227518.5","gene_symbol":"AL928970.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27657,"end":30891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178057.14","gene_symbol":"NDUFAF3","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:29918]","synonyms":"MGC10527,E3-3,DKFZP564J0123,C3orf60,2P1","biotype":"protein_coding","ncbi_id":"25915","summary":"This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]","start":49020459,"end":49023495,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:29918]"}, {"versioned_ensembl_gene_id":"ENSG00000237021.2","gene_symbol":"AL050331.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116254207,"end":116256743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233239.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29923905,"end":29924090,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000234313.2","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"PERB11,HCGIX,HCGIX4,HCGIX-4","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29965045,"end":29968344,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000111817.16","gene_symbol":"DSE","gene_name":"dermatan sulfate epimerase [Source:HGNC Symbol;Acc:HGNC:21144]","synonyms":"SART2,DSEPI,DS-Epi1","biotype":"protein_coding","ncbi_id":"29940","summary":"The protein encoded by this gene is a tumor-rejection antigen. It is localized to the endoplasmic reticulum and functions to convert D-glucuronic acid to L-iduronic acid during the biosynthesis of dermatan sulfate. This antigen possesses tumor epitopes capable of inducing HLA-A24-restricted and tumor-specific cytotoxic T lymphocytes in cancer patients and may be useful for specific immunotherapy. Mutations in this gene cause inmusculocontractural Ehlers-Danlos syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 9, and a paralogous gene exists on chromosome 18. [provided by RefSeq, Apr 2016]","start":116254173,"end":116444860,"strand":1,"description":"dermatan sulfate epimerase [Source:HGNC Symbol;Acc:HGNC:21144]"}, {"versioned_ensembl_gene_id":"ENSG00000040341.17","gene_symbol":"STAU2","gene_name":"staufen double-stranded RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11371]","synonyms":"39K2","biotype":"protein_coding","ncbi_id":"27067","summary":"Staufen homolog 2 is a member of the family of double-stranded RNA (dsRNA)-binding proteins involved in the transport and/or localization of mRNAs to different subcellular compartments and/or organelles. These proteins are characterized by the presence of multiple dsRNA-binding domains which are required to bind RNAs having double-stranded secondary structures. Staufen homolog 2 shares 48.5% and 59.9% similarity with drosophila and human staufen, respectively. The exact function of Staufen homolog 2 is not known, but since it contains 3 copies of conserved dsRNA binding domain, it could be involved in double-stranded RNA binding events. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":73420369,"end":73747708,"strand":-1,"description":"staufen double-stranded RNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:11371]"}, {"versioned_ensembl_gene_id":"ENSG00000229293.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29888173,"end":29889304,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000164120.13","gene_symbol":"HPGD","gene_name":"hydroxyprostaglandin dehydrogenase 15-(NAD) [Source:HGNC Symbol;Acc:HGNC:5154]","synonyms":"SDR36C1","biotype":"protein_coding","ncbi_id":"3248","summary":"This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":174490177,"end":174523154,"strand":-1,"description":"hydroxyprostaglandin dehydrogenase 15-(NAD) [Source:HGNC Symbol;Acc:HGNC:5154]"}, {"versioned_ensembl_gene_id":"ENSG00000236949.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"hZR14,tctex-6,RPA12,HTEX-6","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30049228,"end":30055232,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000239198.1","gene_symbol":"RPL5P22","gene_name":"ribosomal protein L5 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35695]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389644","summary":null,"start":28299683,"end":28300566,"strand":1,"description":"ribosomal protein L5 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:35695]"}, {"versioned_ensembl_gene_id":"ENSG00000234504.2","gene_symbol":"AL353801.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44899614,"end":44920220,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253690.1","gene_symbol":"AC021678.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28250063,"end":28339255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241131.1","gene_symbol":"LINC02032","gene_name":"long intergenic non-protein coding RNA 2032 [Source:HGNC Symbol;Acc:HGNC:52866]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507461","summary":null,"start":148078159,"end":148088029,"strand":1,"description":"long intergenic non-protein coding RNA 2032 [Source:HGNC Symbol;Acc:HGNC:52866]"}, {"versioned_ensembl_gene_id":"ENSG00000223462.2","gene_symbol":"AL353801.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44937508,"end":44955725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237799.2","gene_symbol":"CICP11","gene_name":"capicua transcriptional repressor pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37903]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288904","summary":null,"start":55736779,"end":55739605,"strand":1,"description":"capicua transcriptional repressor pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37903]"}, {"versioned_ensembl_gene_id":"ENSG00000275875.1","gene_symbol":"AC091812.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55741525,"end":55741869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111237.18","gene_symbol":"VPS29","gene_name":"VPS29, retromer complex component [Source:HGNC Symbol;Acc:HGNC:14340]","synonyms":"PEP11,DC7,DC15","biotype":"protein_coding","ncbi_id":"51699","summary":"This gene belongs to a group of vacuolar protein sorting (VPS) genes that, when functionally impaired, disrupt the efficient delivery of vacuolar hydrolases. The protein encoded by this gene is a component of a large multimeric complex, termed the retromer complex, which is involved in retrograde transport of proteins from endosomes to the trans-Golgi network. This VPS protein may be involved in the formation of the inner shell of the retromer coat for retrograde vesicles leaving the prevacuolar compartment. Alternative splice variants encoding different isoforms and representing non-protein coding transcripts have been found for this gene. [provided by RefSeq, Aug 2013]","start":110491097,"end":110502117,"strand":-1,"description":"VPS29, retromer complex component [Source:HGNC Symbol;Acc:HGNC:14340]"}, {"versioned_ensembl_gene_id":"ENSG00000107551.20","gene_symbol":"RASSF4","gene_name":"Ras association domain family member 4 [Source:HGNC Symbol;Acc:HGNC:20793]","synonyms":"MGC44914,AD037","biotype":"protein_coding","ncbi_id":"83937","summary":"The function of this gene has not yet been determined but may involve a role in tumor suppression. Alternative splicing of this gene results in several transcript variants; however, most of the variants have not been fully described. [provided by RefSeq, Jul 2008]","start":44959407,"end":44995891,"strand":1,"description":"Ras association domain family member 4 [Source:HGNC Symbol;Acc:HGNC:20793]"}, {"versioned_ensembl_gene_id":"ENSG00000220125.1","gene_symbol":"MRPL32P1","gene_name":"mitochondrial ribosomal protein L32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29704]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359741","summary":null,"start":48583093,"end":48583339,"strand":-1,"description":"mitochondrial ribosomal protein L32 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29704]"}, {"versioned_ensembl_gene_id":"ENSG00000241792.1","gene_symbol":"AC092958.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148093175,"end":148127233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225548.5","gene_symbol":"LINC01980","gene_name":"long intergenic non-protein coding RNA 1980 [Source:HGNC Symbol;Acc:HGNC:52808]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377007","summary":null,"start":27802762,"end":27891301,"strand":1,"description":"long intergenic non-protein coding RNA 1980 [Source:HGNC Symbol;Acc:HGNC:52808]"}, {"versioned_ensembl_gene_id":"ENSG00000248585.2","gene_symbol":"AC084024.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38201699,"end":38204238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244650.2","gene_symbol":"AC025566.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":148160911,"end":148226606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273720.1","gene_symbol":"AC091812.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55743073,"end":55743457,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205412.5","gene_symbol":"HNRNPA1P20","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39538]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344741","summary":null,"start":148166344,"end":148167298,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:39538]"}, {"versioned_ensembl_gene_id":"ENSG00000156735.10","gene_symbol":"BAG4","gene_name":"BCL2 associated athanogene 4 [Source:HGNC Symbol;Acc:HGNC:940]","synonyms":"SODD","biotype":"protein_coding","ncbi_id":"9530","summary":"The protein encoded by this gene is a member of the BAG1-related protein family. BAG1 is an anti-apoptotic protein that functions through interactions with a variety of cell apoptosis and growth related proteins including BCL-2, Raf-protein kinase, steroid hormone receptors, growth factor receptors and members of the heat shock protein 70 kDa family. This protein contains a BAG domain near the C-terminus, which could bind and inhibit the chaperone activity of Hsc70/Hsp70. This protein was found to be associated with the death domain of tumor necrosis factor receptor type 1 (TNF-R1) and death receptor-3 (DR3), and thereby negatively regulates downstream cell death signaling. The regulatory role of this protein in cell death was demonstrated in epithelial cells which undergo apoptosis while integrin mediated matrix contacts are lost. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011]","start":38176533,"end":38213301,"strand":1,"description":"BCL2 associated athanogene 4 [Source:HGNC Symbol;Acc:HGNC:940]"}, {"versioned_ensembl_gene_id":"ENSG00000228587.1","gene_symbol":"AL049748.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35685940,"end":35689373,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249558.1","gene_symbol":"RCC2P4","gene_name":"regulator of chromosome condensation 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421090","summary":null,"start":126766434,"end":126767475,"strand":-1,"description":"regulator of chromosome condensation 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42380]"}, {"versioned_ensembl_gene_id":"ENSG00000243347.1","gene_symbol":"LINC02045","gene_name":"long intergenic non-protein coding RNA 2045 [Source:HGNC Symbol;Acc:HGNC:52885]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374146","summary":null,"start":148195729,"end":148280098,"strand":-1,"description":"long intergenic non-protein coding RNA 2045 [Source:HGNC Symbol;Acc:HGNC:52885]"}, {"versioned_ensembl_gene_id":"ENSG00000236875.3","gene_symbol":"DDX11L5","gene_name":"DEAD/H-box helicase 11 like 5 [Source:HGNC Symbol;Acc:HGNC:37106]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287596","summary":null,"start":12134,"end":13783,"strand":1,"description":"DEAD/H-box helicase 11 like 5 [Source:HGNC Symbol;Acc:HGNC:37106]"}, {"versioned_ensembl_gene_id":"ENSG00000282723.1","gene_symbol":"MAPK8IP1P1","gene_name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]","synonyms":"MAPK8IPP,PRKM8IPP","biotype":"processed_pseudogene","ncbi_id":"644253","summary":null,"start":46255525,"end":46256963,"strand":1,"description":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6885]"}, {"versioned_ensembl_gene_id":"ENSG00000281927.1","gene_symbol":"AC243899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46271462,"end":46272509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178409.13","gene_symbol":"BEND3","gene_name":"BEN domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23040]","synonyms":"KIAA1553","biotype":"protein_coding","ncbi_id":"57673","summary":null,"start":107065182,"end":107115269,"strand":-1,"description":"BEN domain containing 3 [Source:HGNC Symbol;Acc:HGNC:23040]"}, {"versioned_ensembl_gene_id":"ENSG00000198746.12","gene_symbol":"GPATCH3","gene_name":"G-patch domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25720]","synonyms":"GPATC3,FLJ12455","biotype":"protein_coding","ncbi_id":"63906","summary":null,"start":26890488,"end":26900466,"strand":-1,"description":"G-patch domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25720]"}, {"versioned_ensembl_gene_id":"ENSG00000282032.1","gene_symbol":"AC243899.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46278924,"end":46280579,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235493.1","gene_symbol":"LINC01967","gene_name":"long intergenic non-protein coding RNA 1967 [Source:HGNC Symbol;Acc:HGNC:52793]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986041","summary":null,"start":27997210,"end":28028604,"strand":-1,"description":"long intergenic non-protein coding RNA 1967 [Source:HGNC Symbol;Acc:HGNC:52793]"}, {"versioned_ensembl_gene_id":"ENSG00000226155.1","gene_symbol":"AC124944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":195912049,"end":195913986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238284.1","gene_symbol":"LINC01448","gene_name":"long intergenic non-protein coding RNA 1448 [Source:HGNC Symbol;Acc:HGNC:50790]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928795","summary":null,"start":42661726,"end":42706447,"strand":-1,"description":"long intergenic non-protein coding RNA 1448 [Source:HGNC Symbol;Acc:HGNC:50790]"}, {"versioned_ensembl_gene_id":"ENSG00000231443.2","gene_symbol":"AC124944.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195937243,"end":195938739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109501.13","gene_symbol":"WFS1","gene_name":"wolframin ER transmembrane glycoprotein [Source:HGNC Symbol;Acc:HGNC:12762]","synonyms":"WFS,DIDMOAD,DFNA6,DFNA38,DFNA14","biotype":"protein_coding","ncbi_id":"7466","summary":"This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]","start":6269849,"end":6303265,"strand":1,"description":"wolframin ER transmembrane glycoprotein [Source:HGNC Symbol;Acc:HGNC:12762]"}, {"versioned_ensembl_gene_id":"ENSG00000261342.1","gene_symbol":"AC006538.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2727743,"end":2729327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260261.2","gene_symbol":"AC124944.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":195913078,"end":195954485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229161.2","gene_symbol":"TCP1P1","gene_name":"t-complex 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11659]","synonyms":"TCP1L1","biotype":"unprocessed_pseudogene","ncbi_id":"647047","summary":null,"start":42794906,"end":42802494,"strand":1,"description":"t-complex 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:11659]"}, {"versioned_ensembl_gene_id":"ENSG00000189269.12","gene_symbol":"DRICH1","gene_name":"aspartate rich 1 [Source:HGNC Symbol;Acc:HGNC:28031]","synonyms":"C22orf43","biotype":"protein_coding","ncbi_id":"51233","summary":null,"start":23608452,"end":23632321,"strand":-1,"description":"aspartate rich 1 [Source:HGNC Symbol;Acc:HGNC:28031]"}, {"versioned_ensembl_gene_id":"ENSG00000144867.11","gene_symbol":"SRPRB","gene_name":"SRP receptor beta subunit [Source:HGNC Symbol;Acc:HGNC:24085]","synonyms":"SR-beta,APMCF1","biotype":"protein_coding","ncbi_id":"58477","summary":"The protein encoded by this gene has similarity to mouse protein which is a subunit of the signal recognition particle receptor (SR). This subunit is a transmembrane GTPase belonging to the GTPase superfamily. It anchors alpha subunit, a peripheral membrane GTPase, to the ER membrane. SR is required for the cotranslational targeting of both secretory and membrane proteins to the ER membrane. [provided by RefSeq, Jul 2008]","start":133784033,"end":133825772,"strand":1,"description":"SRP receptor beta subunit [Source:HGNC Symbol;Acc:HGNC:24085]"}, {"versioned_ensembl_gene_id":"ENSG00000176490.4","gene_symbol":"DIRAS1","gene_name":"DIRAS family GTPase 1 [Source:HGNC Symbol;Acc:HGNC:19127]","synonyms":"RIG,GBTS1,Di-Ras1","biotype":"protein_coding","ncbi_id":"148252","summary":"DIRAS1 belongs to a distinct branch of the functionally diverse Ras (see HRAS; MIM 190020) superfamily of monomeric GTPases.[supplied by OMIM, Apr 2004]","start":2714567,"end":2721418,"strand":-1,"description":"DIRAS family GTPase 1 [Source:HGNC Symbol;Acc:HGNC:19127]"}, {"versioned_ensembl_gene_id":"ENSG00000231539.1","gene_symbol":"AC010132.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42829672,"end":42844438,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261019.1","gene_symbol":"AC010132.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42901272,"end":42902639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249235.1","gene_symbol":"AC021146.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68861332,"end":68861610,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240050.5","gene_symbol":"AL590542.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":116280199,"end":116370273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235613.2","gene_symbol":"NSRP1P1","gene_name":"nuclear speckle splicing regulatory protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38087]","synonyms":"CCDC55P1","biotype":"processed_pseudogene","ncbi_id":"100420557","summary":null,"start":77847110,"end":77848802,"strand":1,"description":"nuclear speckle splicing regulatory protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38087]"}, {"versioned_ensembl_gene_id":"ENSG00000232015.2","gene_symbol":"HSPE1P25","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480260","summary":null,"start":77853355,"end":77853893,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 25 [Source:HGNC Symbol;Acc:HGNC:49344]"}, {"versioned_ensembl_gene_id":"ENSG00000233558.1","gene_symbol":"AL050331.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":116258493,"end":116259115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267001.1","gene_symbol":"AC006538.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2717769,"end":2740048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251529.1","gene_symbol":"AC021146.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68877626,"end":68880131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116132.11","gene_symbol":"PRRX1","gene_name":"paired related homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9142]","synonyms":"PMX1,PHOX1","biotype":"protein_coding","ncbi_id":"5396","summary":"The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription co-activator, enhancing the DNA-binding activity of serum response factor, a protein required for the induction of genes by growth and differentiation factors. The protein regulates muscle creatine kinase, indicating a role in the establishment of diverse mesodermal muscle types. Alternative splicing yields two isoforms that differ in abundance and expression patterns. [provided by RefSeq, Jul 2008]","start":170662728,"end":170739419,"strand":1,"description":"paired related homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9142]"}, {"versioned_ensembl_gene_id":"ENSG00000180488.14","gene_symbol":"MIGA1","gene_name":"mitoguardin 1 [Source:HGNC Symbol;Acc:HGNC:24741]","synonyms":"FLJ35093,FAM73A","biotype":"protein_coding","ncbi_id":"374986","summary":null,"start":77779624,"end":77879539,"strand":1,"description":"mitoguardin 1 [Source:HGNC Symbol;Acc:HGNC:24741]"}, {"versioned_ensembl_gene_id":"ENSG00000240627.1","gene_symbol":"AC026798.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51275253,"end":51275734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244723.3","gene_symbol":"ASLP1","gene_name":"argininosuccinate lyase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:747]","synonyms":"ASLL","biotype":"unprocessed_pseudogene","ncbi_id":"436","summary":null,"start":23649213,"end":23653334,"strand":-1,"description":"argininosuccinate lyase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:747]"}, {"versioned_ensembl_gene_id":"ENSG00000141873.10","gene_symbol":"SLC39A3","gene_name":"solute carrier family 39 member 3 [Source:HGNC Symbol;Acc:HGNC:17128]","synonyms":"ZIP3","biotype":"protein_coding","ncbi_id":"29985","summary":null,"start":2732204,"end":2740152,"strand":-1,"description":"solute carrier family 39 member 3 [Source:HGNC Symbol;Acc:HGNC:17128]"}, {"versioned_ensembl_gene_id":"ENSG00000147465.11","gene_symbol":"STAR","gene_name":"steroidogenic acute regulatory protein [Source:HGNC Symbol;Acc:HGNC:11359]","synonyms":"STARD1,StAR","biotype":"protein_coding","ncbi_id":"6770","summary":"The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jul 2008]","start":38143649,"end":38151265,"strand":-1,"description":"steroidogenic acute regulatory protein [Source:HGNC Symbol;Acc:HGNC:11359]"}, {"versioned_ensembl_gene_id":"ENSG00000278052.1","gene_symbol":"AC104985.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34225930,"end":34226429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239930.2","gene_symbol":"AP001625.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42496539,"end":42497443,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000016082.14","gene_symbol":"ISL1","gene_name":"ISL LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6132]","synonyms":"ISLET1,Isl-1","biotype":"protein_coding","ncbi_id":"3670","summary":"This gene encodes a member of the LIM/homeodomain family of transcription factors. The encoded protein binds to the enhancer region of the insulin gene, among others, and may play an important role in regulating insulin gene expression. The encoded protein is central to the development of pancreatic cell lineages and may also be required for motor neuron generation. Mutations in this gene have been associated with maturity-onset diabetes of the young. [provided by RefSeq, Jul 2008]","start":51383391,"end":51394738,"strand":1,"description":"ISL LIM homeobox 1 [Source:HGNC Symbol;Acc:HGNC:6132]"}, {"versioned_ensembl_gene_id":"ENSG00000248547.2","gene_symbol":"AC021146.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68883885,"end":68884440,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277076.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54789863,"end":54800933,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000160190.13","gene_symbol":"SLC37A1","gene_name":"solute carrier family 37 member 1 [Source:HGNC Symbol;Acc:HGNC:11024]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54020","summary":"The protein encoded by this gene localizes to the endoplasmic reticulum (ER) membrane. This protein translocates glucose-6-phosphate from the cytoplasm into the lumen of the ER for hydrolysis into glucose by another ER membrane protein. This gene is a member of the solute carrier 37 gene family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":42496008,"end":42581440,"strand":1,"description":"solute carrier family 37 member 1 [Source:HGNC Symbol;Acc:HGNC:11024]"}, {"versioned_ensembl_gene_id":"ENSG00000277221.2","gene_symbol":"LRRC37A2","gene_name":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]","synonyms":"FLJ45049,FLJ45049","biotype":"protein_coding","ncbi_id":"474170","summary":null,"start":46339497,"end":46384852,"strand":1,"description":"leucine rich repeat containing 37 member A2 [Source:HGNC Symbol;Acc:HGNC:32404]"}, {"versioned_ensembl_gene_id":"ENSG00000262818.1","gene_symbol":"AC055872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6417685,"end":6418264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248813.1","gene_symbol":"AC022447.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31741833,"end":31742327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248878.1","gene_symbol":"AC022447.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":31725539,"end":31725902,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129221.15","gene_symbol":"AIPL1","gene_name":"aryl hydrocarbon receptor interacting protein like 1 [Source:HGNC Symbol;Acc:HGNC:359]","synonyms":"LCA4","biotype":"protein_coding","ncbi_id":"23746","summary":"Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5% of all inherited retinal diseases. Affected individuals are diagnosed at birth or in the first few months of life with nystagmus, severely impaired vision or blindness and an abnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, is located within the LCA4 candidate region. The encoded protein contains three tetratricopeptide motifs, consistent with chaperone or nuclear transport activity. Mutations in this gene may cause approximately 20% of recessive LCA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":6393693,"end":6435199,"strand":-1,"description":"aryl hydrocarbon receptor interacting protein like 1 [Source:HGNC Symbol;Acc:HGNC:359]"}, {"versioned_ensembl_gene_id":"ENSG00000278993.1","gene_symbol":"AC002350.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":110501614,"end":110503441,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124486.12","gene_symbol":"USP9X","gene_name":"ubiquitin specific peptidase 9, X-linked [Source:HGNC Symbol;Acc:HGNC:12632]","synonyms":"MRX99,FAF,DFFRX","biotype":"protein_coding","ncbi_id":"8239","summary":"This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":41085635,"end":41236579,"strand":1,"description":"ubiquitin specific peptidase 9, X-linked [Source:HGNC Symbol;Acc:HGNC:12632]"}, {"versioned_ensembl_gene_id":"ENSG00000260010.1","gene_symbol":"ZNF720P1","gene_name":"zinc finger protein 720 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34505]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"342426","summary":null,"start":31601593,"end":31603531,"strand":-1,"description":"zinc finger protein 720 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:34505]"}, {"versioned_ensembl_gene_id":"ENSG00000177479.19","gene_symbol":"ARIH2","gene_name":"ariadne RBR E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:690]","synonyms":"TRIAD1","biotype":"protein_coding","ncbi_id":"10425","summary":"The protein encoded by this gene is an E3 ubiquitin-protein ligase that polyubiquitinates some proteins, tagging them for degradation. The encoded protein upregulates p53 in some cancer cells and may inhibit myelopoiesis. Several transcript variants encoding different isoforms have been found for this gene, although the full-length nature of some of them have not been determined yet. [provided by RefSeq, Nov 2015]","start":48918821,"end":48986382,"strand":1,"description":"ariadne RBR E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:690]"}, {"versioned_ensembl_gene_id":"ENSG00000229364.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29897735,"end":29898101,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000223860.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29898975,"end":29899837,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000237185.1","gene_symbol":"VN1R66P","gene_name":"vomeronasal 1 receptor 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:37386]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129315","summary":null,"start":31648307,"end":31649222,"strand":1,"description":"vomeronasal 1 receptor 66 pseudogene [Source:HGNC Symbol;Acc:HGNC:37386]"}, {"versioned_ensembl_gene_id":"ENSG00000237783.2","gene_symbol":"AL356441.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165581613,"end":165582476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237463.5","gene_symbol":"AL157714.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165476841,"end":165582155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227418.6","gene_symbol":"PCGEM1","gene_name":"PCGEM1, prostate-specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30145]","synonyms":"PCAT9,NCRNA00071,LINC00071","biotype":"lincRNA","ncbi_id":"64002","summary":"This gene produces a long non-coding RNA that is overexpressed in prostate cancer and may act a marker for tumor progression. This RNA may act a negative regulator of apoptosis, and may promote activity of androgen receptor and Myc. [provided by RefSeq, Dec 2017]","start":192749845,"end":192776899,"strand":1,"description":"PCGEM1, prostate-specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:30145]"}, {"versioned_ensembl_gene_id":"ENSG00000226242.1","gene_symbol":"RPS17P8","gene_name":"ribosomal protein S17 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36772]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271070","summary":null,"start":192774082,"end":192774416,"strand":1,"description":"ribosomal protein S17 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36772]"}, {"versioned_ensembl_gene_id":"ENSG00000154917.10","gene_symbol":"RAB6B","gene_name":"RAB6B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14902]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51560","summary":null,"start":133824239,"end":133895836,"strand":-1,"description":"RAB6B, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:14902]"}, {"versioned_ensembl_gene_id":"ENSG00000229959.1","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29917614,"end":29920391,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000244627.5","gene_symbol":"Z98749.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38335762,"end":38398929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169989.2","gene_symbol":"TIGD4","gene_name":"tigger transposable element derived 4 [Source:HGNC Symbol;Acc:HGNC:18335]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201798","summary":"The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]","start":152769354,"end":152779764,"strand":-1,"description":"tigger transposable element derived 4 [Source:HGNC Symbol;Acc:HGNC:18335]"}, {"versioned_ensembl_gene_id":"ENSG00000236033.3","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"HCG4P6,HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3,bQB90C11.3","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29917138,"end":29918128,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000260631.1","gene_symbol":"RBM22P12","gene_name":"RNA binding motif protein 22 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49207]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131641","summary":null,"start":31680847,"end":31682101,"strand":1,"description":"RNA binding motif protein 22 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:49207]"}, {"versioned_ensembl_gene_id":"ENSG00000219201.4","gene_symbol":"AC138392.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":77810861,"end":77811781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230748.1","gene_symbol":"AL157714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165497724,"end":165498348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162763.3","gene_symbol":"LRRC52","gene_name":"leucine rich repeat containing 52 [Source:HGNC Symbol;Acc:HGNC:32156]","synonyms":"FLJ25811","biotype":"protein_coding","ncbi_id":"440699","summary":null,"start":165544007,"end":165563961,"strand":1,"description":"leucine rich repeat containing 52 [Source:HGNC Symbol;Acc:HGNC:32156]"}, {"versioned_ensembl_gene_id":"ENSG00000175324.9","gene_symbol":"LSM1","gene_name":"LSM1 homolog, mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:20472]","synonyms":"YJL124C,CASM","biotype":"protein_coding","ncbi_id":"27257","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Increased expression of this gene may play a role in cellular transformation and the progression of several malignancies including lung cancer, mesothelioma and breast cancer. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Nov 2011]","start":38163321,"end":38176730,"strand":-1,"description":"LSM1 homolog, mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:20472]"}, {"versioned_ensembl_gene_id":"ENSG00000088035.15","gene_symbol":"ALG6","gene_name":"ALG6, alpha-1,3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23157]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29929","summary":"This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the first glucose residue to the growing lipid-linked oligosaccharide precursor of N-linked glycosylation. Mutations in this gene are associated with congenital disorders of glycosylation type Ic. [provided by RefSeq, Jul 2008]","start":63367590,"end":63438562,"strand":1,"description":"ALG6, alpha-1,3-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:23157]"}, {"versioned_ensembl_gene_id":"ENSG00000153132.12","gene_symbol":"CLGN","gene_name":"calmegin [Source:HGNC Symbol;Acc:HGNC:2060]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1047","summary":"Calmegin is a testis-specific endoplasmic reticulum chaperone protein. CLGN may play a role in spermatogeneisis and infertility. [provided by RefSeq, Jul 2008]","start":140388455,"end":140427968,"strand":-1,"description":"calmegin [Source:HGNC Symbol;Acc:HGNC:2060]"}, {"versioned_ensembl_gene_id":"ENSG00000259663.2","gene_symbol":"AC010478.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51372736,"end":51383332,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220553.1","gene_symbol":"RPL5P19","gene_name":"ribosomal protein L5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36604]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270906","summary":null,"start":92013842,"end":92014734,"strand":1,"description":"ribosomal protein L5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36604]"}, {"versioned_ensembl_gene_id":"ENSG00000261038.1","gene_symbol":"AL133457.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92387841,"end":92388827,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220908.2","gene_symbol":"LINC02531","gene_name":"long intergenic non-protein coding RNA 2531 [Source:HGNC Symbol;Acc:HGNC:53557]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986533","summary":null,"start":92723003,"end":92723829,"strand":-1,"description":"long intergenic non-protein coding RNA 2531 [Source:HGNC Symbol;Acc:HGNC:53557]"}, {"versioned_ensembl_gene_id":"ENSG00000225857.5","gene_symbol":"AL162431.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":180906651,"end":180909166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219387.2","gene_symbol":"ATF1P1","gene_name":"activating transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37691]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128159","summary":null,"start":92887251,"end":92888581,"strand":-1,"description":"activating transcription factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37691]"}, {"versioned_ensembl_gene_id":"ENSG00000271811.1","gene_symbol":"Z97200.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":170667381,"end":170669425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160199.14","gene_symbol":"PKNOX1","gene_name":"PBX/knotted 1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9022]","synonyms":"PREP1","biotype":"protein_coding","ncbi_id":"5316","summary":null,"start":42974510,"end":43033931,"strand":1,"description":"PBX/knotted 1 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9022]"}, {"versioned_ensembl_gene_id":"ENSG00000273363.1","gene_symbol":"AL353801.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":44958917,"end":44959458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224812.2","gene_symbol":"TMEM72-AS1","gene_name":"TMEM72 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27349]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"220980","summary":null,"start":44811024,"end":44959689,"strand":-1,"description":"TMEM72 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27349]"}, {"versioned_ensembl_gene_id":"ENSG00000254921.1","gene_symbol":"AC116456.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8035446,"end":8039718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120210.6","gene_symbol":"INSL6","gene_name":"insulin like 6 [Source:HGNC Symbol;Acc:HGNC:6089]","synonyms":"RIF1","biotype":"protein_coding","ncbi_id":"11172","summary":"The protein encoded by this gene contains a classical signature of the insulin superfamily and is significantly similar to relaxin and relaxin-like factor. This gene is preferentially expressed in testis. Its expression in testis is restricted to interstitial cells surrounding seminiferous tubules, which suggests a role in sperm development and fertilization. [provided by RefSeq, Jul 2008]","start":5131979,"end":5185668,"strand":-1,"description":"insulin like 6 [Source:HGNC Symbol;Acc:HGNC:6089]"}, {"versioned_ensembl_gene_id":"ENSG00000282572.2","gene_symbol":"AC215522.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":19018,"end":35489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155561.14","gene_symbol":"NUP205","gene_name":"nucleoporin 205 [Source:HGNC Symbol;Acc:HGNC:18658]","synonyms":"KIAA0225,C7orf14","biotype":"protein_coding","ncbi_id":"23165","summary":"This gene encodes a nucleoporin, which is a subunit of the nuclear pore complex that functions in active transport of proteins, RNAs and ribonucleoprotein particles between the nucleus and cytoplasm. Mutations in this gene are associated with steroid-resistant nephrotic syndrome. [provided by RefSeq, Jul 2016]","start":135557919,"end":135648757,"strand":1,"description":"nucleoporin 205 [Source:HGNC Symbol;Acc:HGNC:18658]"}, {"versioned_ensembl_gene_id":"ENSG00000166405.14","gene_symbol":"RIC3","gene_name":"RIC3 acetylcholine receptor chaperone [Source:HGNC Symbol;Acc:HGNC:30338]","synonyms":"PRO1385,FLJ11608,AYST720","biotype":"protein_coding","ncbi_id":"79608","summary":"This gene encodes a member of the resistance to inhibitors of cholinesterase 3-like family which functions as a chaperone of specific 5-hydroxytryptamine type 3 receptor and nicotinic acetylcholine receptor subtypes. The encoded protein influences the folding and assembly of these receptor subunits in the endoplasmic reticulum and expression on the cell surface. This protein contains an N-terminal transmembrane domain, a proline-rich spacer, and a cytosolic C-terminal coiled-coil domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":8106093,"end":8169055,"strand":-1,"description":"RIC3 acetylcholine receptor chaperone [Source:HGNC Symbol;Acc:HGNC:30338]"}, {"versioned_ensembl_gene_id":"ENSG00000276276.4","gene_symbol":"ARL17B","gene_name":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]","synonyms":"ARL17","biotype":"protein_coding","ncbi_id":"100506084","summary":null,"start":46286670,"end":46408885,"strand":-1,"description":"ADP ribosylation factor like GTPase 17B [Source:HGNC Symbol;Acc:HGNC:32387]"}, {"versioned_ensembl_gene_id":"ENSG00000122674.11","gene_symbol":"CCZ1","gene_name":"CCZ1 homolog, vacuolar protein trafficking and biogenesis associated [Source:HGNC Symbol;Acc:HGNC:21691]","synonyms":"CGI-43,CCZ1A,C7orf28A","biotype":"protein_coding","ncbi_id":"51622","summary":null,"start":5898725,"end":5926550,"strand":1,"description":"CCZ1 homolog, vacuolar protein trafficking and biogenesis associated [Source:HGNC Symbol;Acc:HGNC:21691]"}, {"versioned_ensembl_gene_id":"ENSG00000276620.1","gene_symbol":"AL591516.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107192300,"end":107192573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145022.4","gene_symbol":"TCTA","gene_name":"T-cell leukemia translocation altered [Source:HGNC Symbol;Acc:HGNC:11692]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6988","summary":null,"start":49412206,"end":49416475,"strand":1,"description":"T-cell leukemia translocation altered [Source:HGNC Symbol;Acc:HGNC:11692]"}, {"versioned_ensembl_gene_id":"ENSG00000220237.1","gene_symbol":"RPS24P12","gene_name":"ribosomal protein S24 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35623]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271098","summary":null,"start":107229759,"end":107230152,"strand":1,"description":"ribosomal protein S24 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35623]"}, {"versioned_ensembl_gene_id":"ENSG00000164494.11","gene_symbol":"PDSS2","gene_name":"decaprenyl diphosphate synthase subunit 2 [Source:HGNC Symbol;Acc:HGNC:23041]","synonyms":"C6orf210,bA59I9.3","biotype":"protein_coding","ncbi_id":"57107","summary":"The protein encoded by this gene is an enzyme that synthesizes the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. Defects in this gene are a cause of coenzyme Q10 deficiency.[provided by RefSeq, Oct 2009]","start":107152557,"end":107459564,"strand":-1,"description":"decaprenyl diphosphate synthase subunit 2 [Source:HGNC Symbol;Acc:HGNC:23041]"}, {"versioned_ensembl_gene_id":"ENSG00000283061.1","gene_symbol":"AC215522.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12704,"end":27234,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243836.5","gene_symbol":"WDR86-AS1","gene_name":"WDR86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41186]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100131176","summary":null,"start":151409161,"end":151413354,"strand":1,"description":"WDR86 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41186]"}, {"versioned_ensembl_gene_id":"ENSG00000165269.12","gene_symbol":"AQP7","gene_name":"aquaporin 7 [Source:HGNC Symbol;Acc:HGNC:640]","synonyms":"AQPap,AQP9,AQP7L","biotype":"protein_coding","ncbi_id":"364","summary":"This gene encodes a member of the aquaporin family of water-selective membrane channels. The encoded protein localizes to the plasma membrane and allows movement of water, glycerol and urea across cell membranes. This gene is highly expressed in the adipose tissue where the encoded protein facilitates efflux of glycerol. In the proximal straight tubules of kidney, the encoded protein is localized to the apical membrane and prevents excretion of glycerol into urine. The encoded protein is present in spermatids, as well as in the testicular and epididymal spermatozoa suggesting an important role in late spermatogenesis. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. This gene is located adjacent to a related aquaporin gene on chromosome 9. Multiple pseudogenes of this gene have been identified. [provided by RefSeq, Dec 2015]","start":33383179,"end":33402682,"strand":-1,"description":"aquaporin 7 [Source:HGNC Symbol;Acc:HGNC:640]"}, {"versioned_ensembl_gene_id":"ENSG00000235099.1","gene_symbol":"AL138731.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93070387,"end":93103384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253356.1","gene_symbol":"AC084024.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38148741,"end":38163772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213187.3","gene_symbol":"COPS5P1","gene_name":"COP9 signalosome subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24332]","synonyms":"COPS5P","biotype":"processed_pseudogene","ncbi_id":"135270","summary":null,"start":93091976,"end":93092760,"strand":-1,"description":"COP9 signalosome subunit 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:24332]"}, {"versioned_ensembl_gene_id":"ENSG00000225695.1","gene_symbol":"HNRNPA1P35","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:48764]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645691","summary":null,"start":201063089,"end":201064051,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:48764]"}, {"versioned_ensembl_gene_id":"ENSG00000236706.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29923501,"end":29923685,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000260568.1","gene_symbol":"AC074050.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31699676,"end":31700465,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232658.1","gene_symbol":"AC092638.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":193256483,"end":193257757,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226517.1","gene_symbol":"CR388220.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29878909,"end":29879877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273772.4","gene_symbol":"SMN2","gene_name":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]","synonyms":"BCD541,TDRD16B,SMNC,GEMIN1","biotype":"protein_coding","ncbi_id":"6607","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Sep 2008]","start":70070287,"end":70099184,"strand":1,"description":"survival of motor neuron 2, centromeric [Source:HGNC Symbol;Acc:HGNC:11118]"}, {"versioned_ensembl_gene_id":"ENSG00000230357.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29899383,"end":29900245,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000155744.9","gene_symbol":"FAM126B","gene_name":"family with sequence similarity 126 member B [Source:HGNC Symbol;Acc:HGNC:28593]","synonyms":"MGC39518,HYCC2","biotype":"protein_coding","ncbi_id":"285172","summary":null,"start":200973718,"end":201071671,"strand":-1,"description":"family with sequence similarity 126 member B [Source:HGNC Symbol;Acc:HGNC:28593]"}, {"versioned_ensembl_gene_id":"ENSG00000234074.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"D6S203,HLA-CDA12,CDA12,HLA-59","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":29996525,"end":29999898,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000236206.1","gene_symbol":"AL356441.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165598463,"end":165623331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129691.15","gene_symbol":"ASH2L","gene_name":"ASH2 like histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:744]","synonyms":"ASH2L1,ASH2,Bre2,ASH2L2","biotype":"protein_coding","ncbi_id":"9070","summary":null,"start":38105242,"end":38144076,"strand":1,"description":"ASH2 like histone lysine methyltransferase complex subunit [Source:HGNC Symbol;Acc:HGNC:744]"}, {"versioned_ensembl_gene_id":"ENSG00000143412.9","gene_symbol":"ANXA9","gene_name":"annexin A9 [Source:HGNC Symbol;Acc:HGNC:547]","synonyms":"ANX31","biotype":"protein_coding","ncbi_id":"8416","summary":"The annexins are a family of calcium-dependent phospholipid-binding proteins. Members of the annexin family contain 4 internal repeat domains, each of which includes a type II calcium-binding site. The calcium-binding sites are required for annexins to aggregate and cooperatively bind anionic phospholipids and extracellular matrix proteins. This gene encodes a divergent member of the annexin protein family in which all four homologous type II calcium-binding sites in the conserved tetrad core contain amino acid substitutions that ablate their function. However, structural analysis suggests that the conserved putative ion channel formed by the tetrad core is intact. [provided by RefSeq, Jul 2008]","start":150982017,"end":150995634,"strand":1,"description":"annexin A9 [Source:HGNC Symbol;Acc:HGNC:547]"}, {"versioned_ensembl_gene_id":"ENSG00000235908.1","gene_symbol":"RHOA-IT1","gene_name":"RHOA intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41308]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"106480739","summary":null,"start":49365145,"end":49367006,"strand":-1,"description":"RHOA intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41308]"}, {"versioned_ensembl_gene_id":"ENSG00000067560.10","gene_symbol":"RHOA","gene_name":"ras homolog family member A [Source:HGNC Symbol;Acc:HGNC:667]","synonyms":"RHOH12,RhoA,Rho12,ARHA,ARH12","biotype":"protein_coding","ncbi_id":"387","summary":"This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. Overexpression of this gene is associated with tumor cell proliferation and metastasis. Multiple alternatively spliced variants have been identified. [provided by RefSeq, Sep 2015]","start":49359145,"end":49412998,"strand":-1,"description":"ras homolog family member A [Source:HGNC Symbol;Acc:HGNC:667]"}, {"versioned_ensembl_gene_id":"ENSG00000253283.1","gene_symbol":"AC091175.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85086615,"end":85087186,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138674.16","gene_symbol":"SEC31A","gene_name":"SEC31 homolog A, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:17052]","synonyms":"SEC31L1,KIAA0905,ABP130,ABP125","biotype":"protein_coding","ncbi_id":"22872","summary":"The protein encoded by this gene shares similarity with the yeast Sec31 protein, and is a component of the outer layer of the coat protein complex II (COPII). The encoded protein is involved in vesicle budding from the endoplasmic reticulum (ER) and contains multiple WD repeats near the N-terminus and a proline-rich region in the C-terminal half. It associates with the protein encoded by the SEC13 homolog, nuclear pore and COPII coat complex component (SEC13), and is required for ER-Golgi transport. Monoubiquitylation of this protein by CUL3-KLHL12 was found to regulate the size of COPII coats to accommodate unusually shaped cargo. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":82818661,"end":82901166,"strand":-1,"description":"SEC31 homolog A, COPII coat complex component [Source:HGNC Symbol;Acc:HGNC:17052]"}, {"versioned_ensembl_gene_id":"ENSG00000156738.17","gene_symbol":"MS4A1","gene_name":"membrane spanning 4-domains A1 [Source:HGNC Symbol;Acc:HGNC:7315]","synonyms":"MS4A2,CD20,Bp35,B1","biotype":"protein_coding","ncbi_id":"931","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This gene encodes a B-lymphocyte surface molecule which plays a role in the development and differentiation of B-cells into plasma cells. This family member is localized to 11q12, among a cluster of family members. Alternative splicing of this gene results in two transcript variants which encode the same protein. [provided by RefSeq, Jul 2008]","start":60455752,"end":60470760,"strand":1,"description":"membrane spanning 4-domains A1 [Source:HGNC Symbol;Acc:HGNC:7315]"}, {"versioned_ensembl_gene_id":"ENSG00000284714.1","gene_symbol":"AC080128.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":133784778,"end":133796640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270234.1","gene_symbol":"AL355333.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8724010,"end":8724288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144034.14","gene_symbol":"TPRKB","gene_name":"TP53RK binding protein [Source:HGNC Symbol;Acc:HGNC:24259]","synonyms":"CGI121,CGI-121","biotype":"protein_coding","ncbi_id":"51002","summary":null,"start":73729104,"end":73737400,"strand":-1,"description":"TP53RK binding protein [Source:HGNC Symbol;Acc:HGNC:24259]"}, {"versioned_ensembl_gene_id":"ENSG00000234752.1","gene_symbol":"AC044784.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8897989,"end":8914596,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187260.15","gene_symbol":"WDR86","gene_name":"WD repeat domain 86 [Source:HGNC Symbol;Acc:HGNC:28020]","synonyms":null,"biotype":"protein_coding","ncbi_id":"349136","summary":null,"start":151375909,"end":151410727,"strand":-1,"description":"WD repeat domain 86 [Source:HGNC Symbol;Acc:HGNC:28020]"}, {"versioned_ensembl_gene_id":"ENSG00000260472.1","gene_symbol":"AC074050.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31697397,"end":31697607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151963.4","gene_symbol":"ZNF37CP","gene_name":"zinc finger protein 37C, pseudogene [Source:HGNC Symbol;Acc:HGNC:29445]","synonyms":"ZNF37C","biotype":"unprocessed_pseudogene","ncbi_id":"79232","summary":null,"start":37883594,"end":37884109,"strand":1,"description":"zinc finger protein 37C, pseudogene [Source:HGNC Symbol;Acc:HGNC:29445]"}, {"versioned_ensembl_gene_id":"ENSG00000179859.9","gene_symbol":"AC104581.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7913324,"end":7916276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228458.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BAT1P2,BPG309N1.15","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29983154,"end":29983550,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000228891.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29898144,"end":29898510,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000235218.2","gene_symbol":"AC092638.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":193276668,"end":193277614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235197.1","gene_symbol":"ZNF33CP","gene_name":"zinc finger protein 33C, pseudogene [Source:HGNC Symbol;Acc:HGNC:30957]","synonyms":"ZNF33AP1,BA393J16.4","biotype":"processed_pseudogene","ncbi_id":"79231","summary":null,"start":37894637,"end":37896666,"strand":1,"description":"zinc finger protein 33C, pseudogene [Source:HGNC Symbol;Acc:HGNC:30957]"}, {"versioned_ensembl_gene_id":"ENSG00000224219.1","gene_symbol":"AC074290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":193730555,"end":193730689,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235657.9","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29879362,"end":29999797,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000234931.1","gene_symbol":"MARK2P15","gene_name":"microtubule affinity regulating kinase 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:45119]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533794","summary":null,"start":83311628,"end":83314475,"strand":-1,"description":"microtubule affinity regulating kinase 2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:45119]"}, {"versioned_ensembl_gene_id":"ENSG00000233945.1","gene_symbol":"AC069540.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83672406,"end":83675439,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223565.1","gene_symbol":"AC069540.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":83735506,"end":83736493,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231867.1","gene_symbol":"AP001625.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42508624,"end":42509661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261731.2","gene_symbol":"AC074050.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31709113,"end":31711984,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276867.1","gene_symbol":"AC074050.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31704728,"end":31705260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233258.1","gene_symbol":"AL390786.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":83911654,"end":83912922,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143409.15","gene_symbol":"MINDY1","gene_name":"MINDY lysine 48 deubiquitinase 1 [Source:HGNC Symbol;Acc:HGNC:25648]","synonyms":"MINDY-1,FLJ11280,FAM63A","biotype":"protein_coding","ncbi_id":"55793","summary":null,"start":150996086,"end":151008375,"strand":-1,"description":"MINDY lysine 48 deubiquitinase 1 [Source:HGNC Symbol;Acc:HGNC:25648]"}, {"versioned_ensembl_gene_id":"ENSG00000235772.1","gene_symbol":"AP001625.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42560374,"end":42561934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131797.12","gene_symbol":"CLUHP3","gene_name":"clustered mitochondria homolog pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:28447]","synonyms":"MGC3020,KIAA0664P3,KIAA0664L3,C16orf67","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132341","summary":null,"start":31700590,"end":31711986,"strand":1,"description":"clustered mitochondria homolog pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:28447]"}, {"versioned_ensembl_gene_id":"ENSG00000212769.5","gene_symbol":"HMGN2P8","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31662]","synonyms":"HMGN2L8,AC022394.1","biotype":"processed_pseudogene","ncbi_id":"100288691","summary":null,"start":84081429,"end":84081995,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:31662]"}, {"versioned_ensembl_gene_id":"ENSG00000237337.1","gene_symbol":"AL592182.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50174306,"end":50175868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160188.9","gene_symbol":"RSPH1","gene_name":"radial spoke head 1 homolog [Source:HGNC Symbol;Acc:HGNC:12371]","synonyms":"TSGA2,RSPH10A,RSP44,FLJ32753,CILD24","biotype":"protein_coding","ncbi_id":"89765","summary":"This gene encodes a male meiotic metaphase chromosome-associated acidic protein. This gene is expressed in tissues with motile cilia or flagella, including the trachea, lungs, airway brushings, and testes. Mutations in this gene result in primary ciliary dyskinesia-24. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]","start":42472486,"end":42496354,"strand":-1,"description":"radial spoke head 1 homolog [Source:HGNC Symbol;Acc:HGNC:12371]"}, {"versioned_ensembl_gene_id":"ENSG00000223808.1","gene_symbol":"AC044784.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8970125,"end":8973468,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237553.1","gene_symbol":"AL133547.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5193339,"end":5193558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275383.1","gene_symbol":"AC126773.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68591382,"end":68594424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115446.11","gene_symbol":"UNC50","gene_name":"unc-50 inner nuclear membrane RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16046]","synonyms":"URP,UNCL,GMH1","biotype":"protein_coding","ncbi_id":"25972","summary":null,"start":98608579,"end":98618515,"strand":1,"description":"unc-50 inner nuclear membrane RNA binding protein [Source:HGNC Symbol;Acc:HGNC:16046]"}, {"versioned_ensembl_gene_id":"ENSG00000232142.1","gene_symbol":"RPS25P9","gene_name":"ribosomal protein S25 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36936]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271373","summary":null,"start":70198988,"end":70199239,"strand":-1,"description":"ribosomal protein S25 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36936]"}, {"versioned_ensembl_gene_id":"ENSG00000263935.1","gene_symbol":"TOMM20P3","gene_name":"TOMM20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50520]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480301","summary":null,"start":8688022,"end":8688410,"strand":-1,"description":"TOMM20 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50520]"}, {"versioned_ensembl_gene_id":"ENSG00000249409.1","gene_symbol":"AC025741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":120639090,"end":120650796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229955.1","gene_symbol":"Z98749.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38387918,"end":38388857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120211.4","gene_symbol":"INSL4","gene_name":"insulin like 4 [Source:HGNC Symbol;Acc:HGNC:6087]","synonyms":"EPIL","biotype":"protein_coding","ncbi_id":"3641","summary":"INSL4 encodes the insulin-like 4 protein, a member of the insulin superfamily. INSL4 encodes a precursor that undergoes post-translational cleavage to produce 3 polypeptide chains, A-C, that form tertiary structures composed of either all three chains, or just the A and B chains. Expression of INSL4 products occurs within the early placental cytotrophoblast and syncytiotrophoblast. [provided by RefSeq, Jul 2008]","start":5231419,"end":5235304,"strand":1,"description":"insulin like 4 [Source:HGNC Symbol;Acc:HGNC:6087]"}, {"versioned_ensembl_gene_id":"ENSG00000256546.1","gene_symbol":"AC156455.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":122063306,"end":122068616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283900.1","gene_symbol":"Z98749.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38291918,"end":38398522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255642.1","gene_symbol":"PABPC1P4","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:8563]","synonyms":"PABPL2,PABPCP5","biotype":"processed_pseudogene","ncbi_id":"341315","summary":null,"start":63822021,"end":63823895,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:8563]"}, {"versioned_ensembl_gene_id":"ENSG00000213923.11","gene_symbol":"CSNK1E","gene_name":"casein kinase 1 epsilon [Source:HGNC Symbol;Acc:HGNC:2453]","synonyms":"CKIepsilon,CKIE,HCKIE","biotype":"protein_coding","ncbi_id":"1454","summary":"The protein encoded by this gene is a serine/threonine protein kinase and a member of the casein kinase I protein family, whose members have been implicated in the control of cytoplasmic and nuclear processes, including DNA replication and repair. The encoded protein is found in the cytoplasm as a monomer and can phosphorylate a variety of proteins, including itself. This protein has been shown to phosphorylate period, a circadian rhythm protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2014]","start":38290691,"end":38318084,"strand":-1,"description":"casein kinase 1 epsilon [Source:HGNC Symbol;Acc:HGNC:2453]"}, {"versioned_ensembl_gene_id":"ENSG00000107014.8","gene_symbol":"RLN2","gene_name":"relaxin 2 [Source:HGNC Symbol;Acc:HGNC:10027]","synonyms":"RLXH2,H2,bA12D24.1.2,bA12D24.1.1","biotype":"protein_coding","ncbi_id":"6019","summary":"This gene encodes a member of the relaxin subfamily and insulin superfamily of peptide hormones. In humans there are three non-allelic relaxin genes. This gene encodes multiple protein isoforms, at least one of which undergoes proteolytic processing. This processing generates relaxin A and B chains that are linked by disulfide bonds to form the mature peptide hormone. This hormone plays a role in the male and female reproductive systems and was initially noted for its role in pregnancy. This protein also plays broader roles in the cardiovascular system, including in the regulation of blood pressure and control of heart rate, and data from animal models shows that this protein may have anti-fibrotic and cardioprotective effects. [provided by RefSeq, Jul 2016]","start":5299868,"end":5304969,"strand":-1,"description":"relaxin 2 [Source:HGNC Symbol;Acc:HGNC:10027]"}, {"versioned_ensembl_gene_id":"ENSG00000255746.1","gene_symbol":"AC007406.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":253442,"end":257299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010379.15","gene_symbol":"SLC6A13","gene_name":"solute carrier family 6 member 13 [Source:HGNC Symbol;Acc:HGNC:11046]","synonyms":"GAT2","biotype":"protein_coding","ncbi_id":"6540","summary":null,"start":220621,"end":262873,"strand":-1,"description":"solute carrier family 6 member 13 [Source:HGNC Symbol;Acc:HGNC:11046]"}, {"versioned_ensembl_gene_id":"ENSG00000180817.11","gene_symbol":"PPA1","gene_name":"pyrophosphatase (inorganic) 1 [Source:HGNC Symbol;Acc:HGNC:9226]","synonyms":"SID6-8061,Ppase,PP1,PP,IOPPP","biotype":"protein_coding","ncbi_id":"5464","summary":"The protein encoded by this gene is a member of the inorganic pyrophosphatase (PPase) family. PPases catalyze the hydrolysis of pyrophosphate to inorganic phosphate, which is important for the phosphate metabolism of cells. Studies of a similar protein in bovine suggested a cytoplasmic localization of this enzyme. [provided by RefSeq, Jul 2008]","start":70202830,"end":70233911,"strand":-1,"description":"pyrophosphatase (inorganic) 1 [Source:HGNC Symbol;Acc:HGNC:9226]"}, {"versioned_ensembl_gene_id":"ENSG00000166402.8","gene_symbol":"TUB","gene_name":"tubby bipartite transcription factor [Source:HGNC Symbol;Acc:HGNC:12406]","synonyms":"rd5","biotype":"protein_coding","ncbi_id":"7275","summary":"This gene encodes a member of the Tubby family of bipartite transcription factors. The encoded protein may play a role in obesity and sensorineural degradation. The crystal structure has been determined for a similar protein in mouse, and it functions as a membrane-bound transcription regulator that translocates to the nucleus in response to phosphoinositide hydrolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":8019244,"end":8106112,"strand":1,"description":"tubby bipartite transcription factor [Source:HGNC Symbol;Acc:HGNC:12406]"}, {"versioned_ensembl_gene_id":"ENSG00000137345.19","gene_symbol":"MOG","gene_name":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]","synonyms":"BTN6,BTNL11","biotype":"protein_coding","ncbi_id":"4340","summary":"The product of this gene is a membrane protein expressed on the oligodendrocyte cell surface and the outermost surface of myelin sheaths. Due to this localization, it is a primary target antigen involved in immune-mediated demyelination. This protein may be involved in completion and maintenance of the myelin sheath and in cell-cell communication. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":29656888,"end":29672280,"strand":1,"description":"myelin oligodendrocyte glycoprotein [Source:HGNC Symbol;Acc:HGNC:7197]"}, {"versioned_ensembl_gene_id":"ENSG00000143457.10","gene_symbol":"GOLPH3L","gene_name":"golgi phosphoprotein 3 like [Source:HGNC Symbol;Acc:HGNC:24882]","synonyms":"GPP34R","biotype":"protein_coding","ncbi_id":"55204","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is localized at the Golgi stack and may have a regulatory role in Golgi trafficking. [provided by RefSeq, Jul 2008]","start":150646225,"end":150697144,"strand":-1,"description":"golgi phosphoprotein 3 like [Source:HGNC Symbol;Acc:HGNC:24882]"}, {"versioned_ensembl_gene_id":"ENSG00000282019.1","gene_symbol":"GPI","gene_name":"glucose-6-phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:4458]","synonyms":"NLK,AMF","biotype":"protein_coding","ncbi_id":"2821","summary":"This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phosphate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","start":34359480,"end":34381539,"strand":1,"description":"glucose-6-phosphate isomerase [Source:HGNC Symbol;Acc:HGNC:4458]"}, {"versioned_ensembl_gene_id":"ENSG00000226336.2","gene_symbol":"MRPS16P3","gene_name":"mitochondrial ribosomal protein S16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29733]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338388","summary":null,"start":35703803,"end":35704176,"strand":1,"description":"mitochondrial ribosomal protein S16 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29733]"}, {"versioned_ensembl_gene_id":"ENSG00000226278.1","gene_symbol":"PSPHP1","gene_name":"phosphoserine phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9578]","synonyms":"PSPHL,CO9","biotype":"unprocessed_pseudogene","ncbi_id":"8781","summary":"This gene is significantly upregulated in Fanconi's anemia fibroblasts but downregulated or absent in fibroblasts from normal donors. It is also highly expressed in FA B-cells of complementation group A. [provided by RefSeq, Jul 2008]","start":55764797,"end":55773288,"strand":1,"description":"phosphoserine phosphatase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9578]"}, {"versioned_ensembl_gene_id":"ENSG00000262730.1","gene_symbol":"AC104581.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7925931,"end":7930622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156966.6","gene_symbol":"B3GNT7","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:18811]","synonyms":"beta3GnT7","biotype":"protein_coding","ncbi_id":"93010","summary":null,"start":231395543,"end":231401164,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 [Source:HGNC Symbol;Acc:HGNC:18811]"}, {"versioned_ensembl_gene_id":"ENSG00000143198.12","gene_symbol":"MGST3","gene_name":"microsomal glutathione S-transferase 3 [Source:HGNC Symbol;Acc:HGNC:7064]","synonyms":"GST-III","biotype":"protein_coding","ncbi_id":"4259","summary":"This gene encodes a member of the MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) protein family. Members of this family are involved in the production of leukotrienes and prostaglandin E, important mediators of inflammation. This gene encodes an enzyme which catalyzes the conjugation of leukotriene A4 and reduced glutathione to produce leukotriene C4. This enzyme also demonstrates glutathione-dependent peroxidase activity towards lipid hydroperoxides.[provided by RefSeq, May 2011]","start":165630861,"end":165661796,"strand":1,"description":"microsomal glutathione S-transferase 3 [Source:HGNC Symbol;Acc:HGNC:7064]"}, {"versioned_ensembl_gene_id":"ENSG00000249753.2","gene_symbol":"AC084357.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":63623788,"end":63795718,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272770.1","gene_symbol":"AC005696.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2683305,"end":2685088,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170043.11","gene_symbol":"TRAPPC1","gene_name":"trafficking protein particle complex 1 [Source:HGNC Symbol;Acc:HGNC:19894]","synonyms":"MUM2,BET5","biotype":"protein_coding","ncbi_id":"58485","summary":"This gene product plays a role in vesicular transport of proteins to the Golgi apparatus from the endoplasmic reticulum. The encoded protein is a component of the multisubunit transport protein particle (TRAPP) complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]","start":7930345,"end":7932123,"strand":-1,"description":"trafficking protein particle complex 1 [Source:HGNC Symbol;Acc:HGNC:19894]"}, {"versioned_ensembl_gene_id":"ENSG00000235259.8","gene_symbol":"TRIM15","gene_name":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]","synonyms":"RNF93,ZNFB7,ZNF178","biotype":"protein_coding","ncbi_id":"89870","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":30155693,"end":30165183,"strand":1,"description":"tripartite motif containing 15 [Source:HGNC Symbol;Acc:HGNC:16284]"}, {"versioned_ensembl_gene_id":"ENSG00000228060.1","gene_symbol":"AL365277.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39565160,"end":39573203,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172799.5","gene_symbol":"ZBTB8OSP2","gene_name":"zinc finger and BTB domain containing 8 opposite strand pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729898","summary":null,"start":231433923,"end":231434426,"strand":-1,"description":"zinc finger and BTB domain containing 8 opposite strand pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:30326]"}, {"versioned_ensembl_gene_id":"ENSG00000273644.1","gene_symbol":"AC215522.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37032,"end":37477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230047.1","gene_symbol":"AC017104.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231437101,"end":231437421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090621.13","gene_symbol":"PABPC4","gene_name":"poly(A) binding protein cytoplasmic 4 [Source:HGNC Symbol;Acc:HGNC:8557]","synonyms":"iPABP,APP-1","biotype":"protein_coding","ncbi_id":"8761","summary":"Poly(A)-binding proteins (PABPs) bind to the poly(A) tail present at the 3-prime ends of most eukaryotic mRNAs. PABPC4 or IPABP (inducible PABP) was isolated as an activation-induced T-cell mRNA encoding a protein. Activation of T cells increased PABPC4 mRNA levels in T cells approximately 5-fold. PABPC4 contains 4 RNA-binding domains and proline-rich C terminus. PABPC4 is localized primarily to the cytoplasm. It is suggested that PABPC4 might be necessary for regulation of stability of labile mRNA species in activated T cells. PABPC4 was also identified as an antigen, APP1 (activated-platelet protein-1), expressed on thrombin-activated rabbit platelets. PABPC4 may also be involved in the regulation of protein translation in platelets and megakaryocytes or may participate in the binding or stabilization of polyadenylates in platelet dense granules. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":39560816,"end":39576790,"strand":-1,"description":"poly(A) binding protein cytoplasmic 4 [Source:HGNC Symbol;Acc:HGNC:8557]"}, {"versioned_ensembl_gene_id":"ENSG00000233538.1","gene_symbol":"AC017104.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":231452195,"end":231453153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242611.2","gene_symbol":"AC093627.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":77038,"end":81178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225907.1","gene_symbol":"RPS27P16","gene_name":"ribosomal protein S27 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36560]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271119","summary":null,"start":30167804,"end":30168004,"strand":1,"description":"ribosomal protein S27 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:36560]"}, {"versioned_ensembl_gene_id":"ENSG00000232325.4","gene_symbol":"AC093627.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70972,"end":95683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240983.1","gene_symbol":"AC090311.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46722975,"end":46723223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270112.3","gene_symbol":"AC090241.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":46756487,"end":46764408,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249868.5","gene_symbol":"AC136777.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":311133,"end":331026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185839.3","gene_symbol":"AL035411.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58630841,"end":58631530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242474.2","gene_symbol":"AC093627.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":135853,"end":149466,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183308.6","gene_symbol":"AC005037.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":200963263,"end":201009102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101638.13","gene_symbol":"ST8SIA5","gene_name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:17827]","synonyms":"SIAT8E","biotype":"protein_coding","ncbi_id":"29906","summary":"The protein encoded by this gene is a type II membrane protein that may be present in the Golgi apparatus. The encoded protein, which is a member of glycosyltransferase family 29, may be involved in the synthesis of gangliosides GD1c, GT1a, GQ1b, and GT3 from GD1a, GT1b, GM1b, and GD3, respectively. [provided by RefSeq, Jul 2008]","start":46667821,"end":46759257,"strand":-1,"description":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:17827]"}, {"versioned_ensembl_gene_id":"ENSG00000226658.1","gene_symbol":"RPL23AP30","gene_name":"ribosomal protein L23a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271459","summary":null,"start":201066691,"end":201067191,"strand":1,"description":"ribosomal protein L23a pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35617]"}, {"versioned_ensembl_gene_id":"ENSG00000119013.8","gene_symbol":"NDUFB3","gene_name":"NADH:ubiquinone oxidoreductase subunit B3 [Source:HGNC Symbol;Acc:HGNC:7698]","synonyms":"B12","biotype":"protein_coding","ncbi_id":"4709","summary":"This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene. [provided by RefSeq, Mar 2012]","start":201071433,"end":201085750,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B3 [Source:HGNC Symbol;Acc:HGNC:7698]"}, {"versioned_ensembl_gene_id":"ENSG00000260142.1","gene_symbol":"AC068135.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":193898367,"end":193899394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182366.9","gene_symbol":"FAM87A","gene_name":"family with sequence similarity 87 member A [Source:NCBI gene;Acc:157693]","synonyms":null,"biotype":"lincRNA","ncbi_id":"157693","summary":null,"start":375931,"end":383174,"strand":-1,"description":"family with sequence similarity 87 member A [Source:NCBI gene;Acc:157693]"}, {"versioned_ensembl_gene_id":"ENSG00000224670.1","gene_symbol":"AC068135.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":194027919,"end":194028164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170049.9","gene_symbol":"KCNAB3","gene_name":"potassium voltage-gated channel subfamily A regulatory beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:6230]","synonyms":"KCNA3B,AKR6A9","biotype":"protein_coding","ncbi_id":"9196","summary":"This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. The encoded protein is one of the beta subunits, which are auxiliary proteins associating with functional Kv-alpha subunits. The encoded protein forms a heterodimer with the potassium voltage-gated channel, shaker-related subfamily, member 5 gene product and regulates the activity of the alpha subunit. [provided by RefSeq, May 2012]","start":7921859,"end":7929803,"strand":-1,"description":"potassium voltage-gated channel subfamily A regulatory beta subunit 3 [Source:HGNC Symbol;Acc:HGNC:6230]"}, {"versioned_ensembl_gene_id":"ENSG00000115216.13","gene_symbol":"NRBP1","gene_name":"nuclear receptor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7993]","synonyms":"NRBP,MUDPNP,MADM,BCON3","biotype":"protein_coding","ncbi_id":"29959","summary":null,"start":27427790,"end":27442259,"strand":1,"description":"nuclear receptor binding protein 1 [Source:HGNC Symbol;Acc:HGNC:7993]"}, {"versioned_ensembl_gene_id":"ENSG00000281567.1","gene_symbol":"SLC25A51P1","gene_name":"solute carrier family 25 member 51 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23325]","synonyms":"bA707M13.1,MCART3P","biotype":"processed_pseudogene","ncbi_id":"442229","summary":null,"start":65788417,"end":65789287,"strand":1,"description":"solute carrier family 25 member 51 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23325]"}, {"versioned_ensembl_gene_id":"ENSG00000248840.2","gene_symbol":"AL645949.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":3312512,"end":3313058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237406.1","gene_symbol":"NDUFA9P1","gene_name":"NADH:ubiquinone oxidoreductase subunit A9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19252]","synonyms":"dJ106I20.2","biotype":"processed_pseudogene","ncbi_id":"266625","summary":null,"start":35897270,"end":35898404,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A9 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19252]"}, {"versioned_ensembl_gene_id":"ENSG00000236315.6","gene_symbol":"NCR3","gene_name":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]","synonyms":"1C7,LY117,CD337,NKp30","biotype":"protein_coding","ncbi_id":"259197","summary":"The protein encoded by this gene is a natural cytotoxicity receptor (NCR) that may aid NK cells in the lysis of tumor cells. The encoded protein interacts with CD3-zeta (CD247), a T-cell receptor. A single nucleotide polymorphism in the 5' untranslated region of this gene has been associated with mild malaria suceptibility. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]","start":31655881,"end":31659971,"strand":-1,"description":"natural cytotoxicity triggering receptor 3 [Source:HGNC Symbol;Acc:HGNC:19077]"}, {"versioned_ensembl_gene_id":"ENSG00000248843.1","gene_symbol":"AL645949.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3323977,"end":3324762,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277364.2","gene_symbol":"ADH5P4","gene_name":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21377]","synonyms":"bA707M13.2,ADH5B","biotype":"processed_pseudogene","ncbi_id":"642443","summary":null,"start":65836930,"end":65838039,"strand":-1,"description":"alcohol dehydrogenase 5 (class III), chi polypeptide, pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21377]"}, {"versioned_ensembl_gene_id":"ENSG00000275887.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"CD158C,KIRX,KIR48,KIR3DS2P,KIR2DS6","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54771283,"end":54784696,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000240859.1","gene_symbol":"AC093627.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":149597,"end":155465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159788.18","gene_symbol":"RGS12","gene_name":"regulator of G protein signaling 12 [Source:HGNC Symbol;Acc:HGNC:9994]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6002","summary":"This gene encodes a member of the 'regulator of G protein signaling' (RGS) gene family. The encoded protein may function as a guanosine triphosphatase (GTPase)-activating protein as well as a transcriptional repressor. This protein may play a role in tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]","start":3293028,"end":3439913,"strand":1,"description":"regulator of G protein signaling 12 [Source:HGNC Symbol;Acc:HGNC:9994]"}, {"versioned_ensembl_gene_id":"ENSG00000236910.1","gene_symbol":"ZNF70P1","gene_name":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]","synonyms":"dJ1033B10.7,bCX269C15.3,ZNF314P","biotype":"processed_pseudogene","ncbi_id":"100419609","summary":null,"start":33369589,"end":33370212,"strand":1,"description":"zinc finger protein 70 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13846]"}, {"versioned_ensembl_gene_id":"ENSG00000242960.1","gene_symbol":"FTH1P23","gene_name":"ferritin heavy chain 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37641]","synonyms":"FTHL23","biotype":"processed_pseudogene","ncbi_id":"100420300","summary":null,"start":72929044,"end":72929593,"strand":1,"description":"ferritin heavy chain 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:37641]"}, {"versioned_ensembl_gene_id":"ENSG00000125249.6","gene_symbol":"RAP2A","gene_name":"RAP2A, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9861]","synonyms":"RAP2,K-REV","biotype":"protein_coding","ncbi_id":"5911","summary":null,"start":97434222,"end":97469128,"strand":1,"description":"RAP2A, member of RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:9861]"}, {"versioned_ensembl_gene_id":"ENSG00000229239.2","gene_symbol":"AL451000.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23670294,"end":23680259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136758.18","gene_symbol":"YME1L1","gene_name":"YME1 like 1 ATPase [Source:HGNC Symbol;Acc:HGNC:12843]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10730","summary":"The protein encoded by this gene is the human ortholog of yeast mitochondrial AAA metalloprotease, Yme1p. It is localized in the mitochondria and can functionally complement a yme1 disruptant yeast strain. It is proposed that this gene plays a role in mitochondrial protein metabolism and could be involved in mitochondrial pathologies. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":27110112,"end":27155266,"strand":-1,"description":"YME1 like 1 ATPase [Source:HGNC Symbol;Acc:HGNC:12843]"}, {"versioned_ensembl_gene_id":"ENSG00000276209.4","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"CD158i,KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54819179,"end":54834168,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000128313.2","gene_symbol":"APOL5","gene_name":"apolipoprotein L5 [Source:HGNC Symbol;Acc:HGNC:14869]","synonyms":"APOLV","biotype":"protein_coding","ncbi_id":"80831","summary":"This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. [provided by RefSeq, Jul 2008]","start":35717872,"end":35729483,"strand":1,"description":"apolipoprotein L5 [Source:HGNC Symbol;Acc:HGNC:14869]"}, {"versioned_ensembl_gene_id":"ENSG00000280814.1","gene_symbol":"AL356432.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127654860,"end":127655278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261795.1","gene_symbol":"AC093627.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":161765,"end":164972,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213171.2","gene_symbol":"LINGO4","gene_name":"leucine rich repeat and Ig domain containing 4 [Source:HGNC Symbol;Acc:HGNC:31814]","synonyms":"LRRN6D","biotype":"protein_coding","ncbi_id":"339398","summary":null,"start":151800264,"end":151806154,"strand":-1,"description":"leucine rich repeat and Ig domain containing 4 [Source:HGNC Symbol;Acc:HGNC:31814]"}, {"versioned_ensembl_gene_id":"ENSG00000163605.14","gene_symbol":"PPP4R2","gene_name":"protein phosphatase 4 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:18296]","synonyms":null,"biotype":"protein_coding","ncbi_id":"151987","summary":"The protein encoded by this gene is a regulatory subunit of the serine/threonine-protein phosphatase 4 complex. In addition to being required for efficient DNA double strand break repair, this complex plays a role in organization of microtubules at centrosomes and processing of spliceosomal snRNPs. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]","start":72996785,"end":73069199,"strand":1,"description":"protein phosphatase 4 regulatory subunit 2 [Source:HGNC Symbol;Acc:HGNC:18296]"}, {"versioned_ensembl_gene_id":"ENSG00000274146.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54802891,"end":54817199,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000224735.1","gene_symbol":"BX323845.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53759026,"end":53759204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280658.1","gene_symbol":"AL356432.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127659425,"end":127660338,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276704.1","gene_symbol":"AL442067.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":97437268,"end":97437630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261580.1","gene_symbol":"ENPP7P13","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48696]","synonyms":"DUNQU1","biotype":"processed_pseudogene","ncbi_id":"104644205","summary":null,"start":33769421,"end":33769679,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:48696]"}, {"versioned_ensembl_gene_id":"ENSG00000283057.1","gene_symbol":"AC010653.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71777603,"end":71777834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255734.1","gene_symbol":"HNRNPABP1","gene_name":"heterogeneous nuclear ribonucleoprotein A/B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48744]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390294","summary":null,"start":10111738,"end":10112471,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A/B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48744]"}, {"versioned_ensembl_gene_id":"ENSG00000281054.1","gene_symbol":"AL356432.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127659690,"end":127660579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276573.1","gene_symbol":"AL442067.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":97435946,"end":97436168,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241669.1","gene_symbol":"LINC01327","gene_name":"long intergenic non-protein coding RNA 1327 [Source:HGNC Symbol;Acc:HGNC:50533]","synonyms":"TCONS_00005644","biotype":"lincRNA","ncbi_id":"104310350","summary":null,"start":167392796,"end":167408519,"strand":1,"description":"long intergenic non-protein coding RNA 1327 [Source:HGNC Symbol;Acc:HGNC:50533]"}, {"versioned_ensembl_gene_id":"ENSG00000226110.2","gene_symbol":"BX323845.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53768986,"end":53769219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239715.1","gene_symbol":"AC093627.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174920,"end":176013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166747.12","gene_symbol":"AP1G1","gene_name":"adaptor related protein complex 1 gamma 1 subunit [Source:HGNC Symbol;Acc:HGNC:555]","synonyms":"CLAPG1,ADTG","biotype":"protein_coding","ncbi_id":"164","summary":"Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes. The adaptin family of proteins is composed of four classes of molecules named alpha, beta-, beta prime- and gamma- adaptins. Adaptins, together with medium and small subunits, form a heterotetrameric complex called an adaptor, whose role is to promote the formation of clathrin-coated pits and vesicles. The protein encoded by this gene is a gamma-adaptin protein and it belongs to the adaptor complexes large subunits family. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":71729000,"end":71809201,"strand":-1,"description":"adaptor related protein complex 1 gamma 1 subunit [Source:HGNC Symbol;Acc:HGNC:555]"}, {"versioned_ensembl_gene_id":"ENSG00000234149.1","gene_symbol":"AC018511.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75003055,"end":75025174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227186.1","gene_symbol":"AC018511.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75023475,"end":75024251,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115942.8","gene_symbol":"ORC2","gene_name":"origin recognition complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:8488]","synonyms":"ORC2L","biotype":"protein_coding","ncbi_id":"4999","summary":"The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. This protein forms a core complex with ORC3, -4, and -5. It also interacts with CDC45 and MCM10, which are proteins known to be important for the initiation of DNA replication. This protein has been demonstrated to specifically associate with the origin of replication of Epstein-Barr virus in human cells, and is thought to be required for DNA replication from viral origin of replication. Alternatively spliced transcript variants have been found, one of which is a nonsense-mediated mRNA decay candidate. [provided by RefSeq, Oct 2010]","start":200908973,"end":200963680,"strand":-1,"description":"origin recognition complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:8488]"}, {"versioned_ensembl_gene_id":"ENSG00000154997.8","gene_symbol":"SEPT14","gene_name":"septin 14 [Source:HGNC Symbol;Acc:HGNC:33280]","synonyms":"FLJ44060","biotype":"protein_coding","ncbi_id":"346288","summary":"SEPT14 is a member of the highly conserved septin family of GTP-binding cytoskeletal proteins implicated in membrane transport, apoptosis, cell polarity, cell cycle regulation, cytokinesis, and other cellular functions (Peterson et al., 2007 [PubMed 17922164]).[supplied by OMIM, Jul 2008]","start":55793544,"end":55862789,"strand":-1,"description":"septin 14 [Source:HGNC Symbol;Acc:HGNC:33280]"}, {"versioned_ensembl_gene_id":"ENSG00000112559.13","gene_symbol":"MDFI","gene_name":"MyoD family inhibitor [Source:HGNC Symbol;Acc:HGNC:6967]","synonyms":"I-mfa","biotype":"protein_coding","ncbi_id":"4188","summary":"This protein is a transcription factor that negatively regulates other myogenic family proteins. Studies of the mouse homolog, I-mf, show that it interferes with myogenic factor function by masking nuclear localization signals and preventing DNA binding. Knockout mouse studies show defects in the formation of vertebrae and ribs that also involve cartilage formation in these structures. [provided by RefSeq, Jul 2008]","start":41636882,"end":41654246,"strand":1,"description":"MyoD family inhibitor [Source:HGNC Symbol;Acc:HGNC:6967]"}, {"versioned_ensembl_gene_id":"ENSG00000177706.8","gene_symbol":"FAM20C","gene_name":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]","synonyms":"IMAGE:4942737,G-CK,DMP4,DKFZp547D065","biotype":"protein_coding","ncbi_id":"56975","summary":"This gene encodes a member of the family of secreted protein kinases. The encoded protein binds calcium and phosphorylates proteins involved in bone mineralization. Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Apr 2014]","start":192969,"end":260745,"strand":1,"description":"FAM20C, golgi associated secretory pathway kinase [Source:HGNC Symbol;Acc:HGNC:22140]"}, {"versioned_ensembl_gene_id":"ENSG00000179085.7","gene_symbol":"DPM3","gene_name":"dolichyl-phosphate mannosyltransferase subunit 3 [Source:HGNC Symbol;Acc:HGNC:3007]","synonyms":"MGC34275,MGC125905,MGC125904","biotype":"protein_coding","ncbi_id":"54344","summary":"Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. The protein encoded by this gene is a subunit of dolichyl-phosphate mannosyltransferase and acts as a stabilizer subunit of the dolichyl-phosphate mannosyltransferase complex. [provided by RefSeq, Jul 2008]","start":155139891,"end":155140595,"strand":-1,"description":"dolichyl-phosphate mannosyltransferase subunit 3 [Source:HGNC Symbol;Acc:HGNC:3007]"}, {"versioned_ensembl_gene_id":"ENSG00000255583.2","gene_symbol":"AC084357.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63682523,"end":63724935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000007168.12","gene_symbol":"PAFAH1B1","gene_name":"platelet activating factor acetylhydrolase 1b regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:8574]","synonyms":"PAFAH,NudF,MDS,MDCR,LIS1","biotype":"protein_coding","ncbi_id":"5048","summary":"This locus was identified as encoding a gene that when mutated or lost caused the lissencephaly associated with Miller-Dieker lissencephaly syndrome. This gene encodes the non-catalytic alpha subunit of the intracellular Ib isoform of platelet-activating factor acteylhydrolase, a heterotrimeric enzyme that specifically catalyzes the removal of the acetyl group at the SN-2 position of platelet-activating factor (identified as 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine). Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist: one composed of multiple subunits, the other, a single subunit. In addition, a single-subunit isoform of this enzyme is found in serum. [provided by RefSeq, Apr 2009]","start":2593210,"end":2685615,"strand":1,"description":"platelet activating factor acetylhydrolase 1b regulatory subunit 1 [Source:HGNC Symbol;Acc:HGNC:8574]"}, {"versioned_ensembl_gene_id":"ENSG00000257005.1","gene_symbol":"AC027667.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63651627,"end":63651930,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253495.1","gene_symbol":"CYCSP23","gene_name":"cytochrome c, somatic pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:24397]","synonyms":"HCP23","biotype":"processed_pseudogene","ncbi_id":"360176","summary":null,"start":119618162,"end":119618474,"strand":-1,"description":"cytochrome c, somatic pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:24397]"}, {"versioned_ensembl_gene_id":"ENSG00000177990.11","gene_symbol":"DPY19L2","gene_name":"dpy-19 like 2 [Source:HGNC Symbol;Acc:HGNC:19414]","synonyms":"SPATA34,FLJ32949","biotype":"protein_coding","ncbi_id":"283417","summary":"The protein encoded by this gene belongs to the dpy-19 family. It is highly expressed in testis, and is required for sperm head elongation and acrosome formation during spermatogenesis. Mutations in this gene are associated with an infertility disorder, spermatogenic failure type 9 (SPGF9). [provided by RefSeq, Dec 2011]","start":63558913,"end":63668939,"strand":-1,"description":"dpy-19 like 2 [Source:HGNC Symbol;Acc:HGNC:19414]"}, {"versioned_ensembl_gene_id":"ENSG00000170037.13","gene_symbol":"CNTROB","gene_name":"centrobin, centriole duplication and spindle assembly protein [Source:HGNC Symbol;Acc:HGNC:29616]","synonyms":"PP1221,LIP8","biotype":"protein_coding","ncbi_id":"116840","summary":"This gene encodes a centrosomal protein that interacts with BRCA2, and is required for centriole duplication and cytokinesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":7932101,"end":7949918,"strand":1,"description":"centrobin, centriole duplication and spindle assembly protein [Source:HGNC Symbol;Acc:HGNC:29616]"}, {"versioned_ensembl_gene_id":"ENSG00000136960.12","gene_symbol":"ENPP2","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:3357]","synonyms":"PDNP2,PD-IALPHA,ATX","biotype":"protein_coding","ncbi_id":"5168","summary":"The protein encoded by this gene functions as both a phosphodiesterase, which cleaves phosphodiester bonds at the 5' end of oligonucleotides, and a phospholipase, which catalyzes production of lysophosphatidic acid (LPA) in extracellular fluids. LPA evokes growth factor-like responses including stimulation of cell proliferation and chemotaxis. This gene product stimulates the motility of tumor cells and has angiogenic properties, and its expression is upregulated in several kinds of carcinomas. The gene product is secreted and further processed to make the biologically active form. Several alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2008]","start":119557086,"end":119673453,"strand":-1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 2 [Source:HGNC Symbol;Acc:HGNC:3357]"}, {"versioned_ensembl_gene_id":"ENSG00000265962.1","gene_symbol":"GACAT2","gene_name":"gastric cancer associated transcript 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50516]","synonyms":"MTCL1-AS1,HMlincRNA717","biotype":"antisense_RNA","ncbi_id":"100287082","summary":null,"start":8695856,"end":8707621,"strand":-1,"description":"gastric cancer associated transcript 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:50516]"}, {"versioned_ensembl_gene_id":"ENSG00000255423.1","gene_symbol":"EBLN2","gene_name":"endogenous Bornavirus like nucleoprotein 2 [Source:HGNC Symbol;Acc:HGNC:25493]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55096","summary":null,"start":73061659,"end":73063337,"strand":1,"description":"endogenous Bornavirus like nucleoprotein 2 [Source:HGNC Symbol;Acc:HGNC:25493]"}, {"versioned_ensembl_gene_id":"ENSG00000272788.1","gene_symbol":"AP000864.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":8801656,"end":8802305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172986.12","gene_symbol":"GXYLT2","gene_name":"glucoside xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:33383]","synonyms":"GLT8D4","biotype":"protein_coding","ncbi_id":"727936","summary":"The protein encoded by this gene is a xylosyltransferase that elongates O-linked glucose bound to epidermal growth factor (EGF) repeats. The encoded protein catalyzes the addition of xylose to the O-glucose-modified residues of EGF repeats of Notch proteins. [provided by RefSeq, Sep 2016]","start":72888073,"end":72998138,"strand":1,"description":"glucoside xylosyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:33383]"}, {"versioned_ensembl_gene_id":"ENSG00000225270.1","gene_symbol":"CICP12","gene_name":"capicua transcriptional repressor pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37905]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420224","summary":null,"start":55798034,"end":55798876,"strand":1,"description":"capicua transcriptional repressor pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37905]"}, {"versioned_ensembl_gene_id":"ENSG00000229762.1","gene_symbol":"AC092647.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55810779,"end":55811411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214195.4","gene_symbol":"HMGN2P31","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39398]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"645930","summary":null,"start":5311444,"end":5311716,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39398]"}, {"versioned_ensembl_gene_id":"ENSG00000283297.1","gene_symbol":"AC005841.2","gene_name":"Uncharacterized protein ENSP00000372125 [Source:UniProtKB/Swiss-Prot;Acc:A6NCN8]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":2849039,"end":2857083,"strand":-1,"description":"Uncharacterized protein ENSP00000372125 [Source:UniProtKB/Swiss-Prot;Acc:A6NCN8]"}, {"versioned_ensembl_gene_id":"ENSG00000235738.1","gene_symbol":"AC092647.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55797946,"end":55798480,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168502.17","gene_symbol":"MTCL1","gene_name":"microtubule crosslinking factor 1 [Source:HGNC Symbol;Acc:HGNC:29121]","synonyms":"SOGA2,KIAA0802,CCDC165","biotype":"protein_coding","ncbi_id":"23255","summary":null,"start":8705661,"end":8832778,"strand":1,"description":"microtubule crosslinking factor 1 [Source:HGNC Symbol;Acc:HGNC:29121]"}, {"versioned_ensembl_gene_id":"ENSG00000256271.1","gene_symbol":"CACNA1C-AS2","gene_name":"CACNA1C antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40118]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874235","summary":null,"start":2668500,"end":2672220,"strand":-1,"description":"CACNA1C antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40118]"}, {"versioned_ensembl_gene_id":"ENSG00000223452.3","gene_symbol":"HMGN2P18","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39382]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"648822","summary":null,"start":155148544,"end":155148813,"strand":1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:39382]"}, {"versioned_ensembl_gene_id":"ENSG00000229037.2","gene_symbol":"BX323845.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53807776,"end":53808623,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246627.6","gene_symbol":"CACNA1C-AS1","gene_name":"CACNA1C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40119]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652846","summary":null,"start":2676001,"end":2691200,"strand":-1,"description":"CACNA1C antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40119]"}, {"versioned_ensembl_gene_id":"ENSG00000248332.6","gene_symbol":"TUB-AS1","gene_name":"TUB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51120]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"101927917","summary":null,"start":8060038,"end":8069373,"strand":1,"description":"TUB antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51120]"}, {"versioned_ensembl_gene_id":"ENSG00000071203.9","gene_symbol":"MS4A12","gene_name":"membrane spanning 4-domains A12 [Source:HGNC Symbol;Acc:HGNC:13370]","synonyms":"Ms4a10,FLJ20217","biotype":"protein_coding","ncbi_id":"54860","summary":"The protein encoded by this gene is a cell surface protein found primarily in the apical membrane of colonocytes. Silencing of this gene in colon cancer cells inhibits the proliferation, cell motility, and chemotactic invasion of cells. This gene is part of a cluster of similar genes found on chromosome 11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]","start":60492778,"end":60507430,"strand":1,"description":"membrane spanning 4-domains A12 [Source:HGNC Symbol;Acc:HGNC:13370]"}, {"versioned_ensembl_gene_id":"ENSG00000142676.12","gene_symbol":"RPL11","gene_name":"ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:10301]","synonyms":"L11","biotype":"protein_coding","ncbi_id":"6135","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L5P family of ribosomal proteins. It is located in the cytoplasm. The protein probably associates with the 5S rRNA. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Dec 2010]","start":23691779,"end":23696425,"strand":1,"description":"ribosomal protein L11 [Source:HGNC Symbol;Acc:HGNC:10301]"}, {"versioned_ensembl_gene_id":"ENSG00000240093.1","gene_symbol":"AC093627.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":182935,"end":194180,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196299.10","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":29990282,"end":30052027,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000106591.3","gene_symbol":"MRPL32","gene_name":"mitochondrial ribosomal protein L32 [Source:HGNC Symbol;Acc:HGNC:14035]","synonyms":"MRP-L32,L32mt,HSPC283,bMRP-59b","biotype":"protein_coding","ncbi_id":"64983","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L32 ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome Xp. [provided by RefSeq, Jul 2008]","start":42932200,"end":42948958,"strand":1,"description":"mitochondrial ribosomal protein L32 [Source:HGNC Symbol;Acc:HGNC:14035]"}, {"versioned_ensembl_gene_id":"ENSG00000213339.8","gene_symbol":"QTRT1","gene_name":"queuine tRNA-ribosyltransferase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:23797]","synonyms":"TGT","biotype":"protein_coding","ncbi_id":"81890","summary":"This gene encodes the catalytic subunit of tRNA-guanine transglycosylase. tRNA-guanine transglycosylase is a heterodimeric enzyme complex that plays a critical role in tRNA modification by synthesizing the 7-deazaguanosine queuosine, which is found in tRNAs that code for asparagine, aspartic acid, histidine and tyrosine. A pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, Feb 2012]","start":10701430,"end":10713437,"strand":1,"description":"queuine tRNA-ribosyltransferase catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:23797]"}, {"versioned_ensembl_gene_id":"ENSG00000249852.1","gene_symbol":"AC145676.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":227554,"end":229557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255669.2","gene_symbol":"AC092471.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":2761200,"end":2775658,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281270.1","gene_symbol":"LINC02536","gene_name":"long intergenic non-protein coding RNA 2536 [Source:HGNC Symbol;Acc:HGNC:53570]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377997","summary":null,"start":127664554,"end":127681555,"strand":1,"description":"long intergenic non-protein coding RNA 2536 [Source:HGNC Symbol;Acc:HGNC:53570]"}, {"versioned_ensembl_gene_id":"ENSG00000279391.1","gene_symbol":"AC116456.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8075573,"end":8077781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281380.1","gene_symbol":"AC244635.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70115323,"end":70149120,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256721.1","gene_symbol":"CACNA1C-IT3","gene_name":"CACNA1C intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:41314]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874370","summary":null,"start":2269776,"end":2288937,"strand":1,"description":"CACNA1C intronic transcript 3 [Source:HGNC Symbol;Acc:HGNC:41314]"}, {"versioned_ensembl_gene_id":"ENSG00000280983.1","gene_symbol":"AC244635.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70153366,"end":70153660,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256257.1","gene_symbol":"CACNA1C-IT2","gene_name":"CACNA1C intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41313]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874369","summary":null,"start":2048352,"end":2049463,"strand":1,"description":"CACNA1C intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:41313]"}, {"versioned_ensembl_gene_id":"ENSG00000127472.10","gene_symbol":"PLA2G5","gene_name":"phospholipase A2 group V [Source:HGNC Symbol;Acc:HGNC:9038]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5322","summary":"This gene is a member of the secretory phospholipase A2 family. It is located in a tightly-linked cluster of secretory phospholipase A2 genes on chromosome 1. The encoded enzyme catalyzes the hydrolysis of membrane phospholipids to generate lysophospholipids and free fatty acids including arachidonic acid. It preferentially hydrolyzes linoleoyl-containing phosphatidylcholine substrates. Secretion of this enzyme is thought to induce inflammatory responses in neighboring cells. Alternatively spliced transcript variants have been found, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":20028179,"end":20091190,"strand":1,"description":"phospholipase A2 group V [Source:HGNC Symbol;Acc:HGNC:9038]"}, {"versioned_ensembl_gene_id":"ENSG00000256646.7","gene_symbol":"AC010132.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42909273,"end":42932174,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078246.16","gene_symbol":"TULP3","gene_name":"tubby like protein 3 [Source:HGNC Symbol;Acc:HGNC:12425]","synonyms":"TUBL3","biotype":"protein_coding","ncbi_id":"7289","summary":"This gene encodes a member of the tubby gene family of bipartite transcription factors. Members of this family have been identified in plants, vertebrates, and invertebrates, and they share a conserved N-terminal transcription activation region and a conserved C-terminal DNA and phosphatidylinositol-phosphate binding region. The encoded protein binds to phosphoinositides in the plasma membrane via its C-terminal region and probably functions as a membrane-bound transcription regulator that translocates to the nucleus in response to phosphoinositide hydrolysis, for instance, induced by G-protein-coupled-receptor signaling. It plays an important role in neuronal development and function. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, May 2009]","start":2877223,"end":2941140,"strand":1,"description":"tubby like protein 3 [Source:HGNC Symbol;Acc:HGNC:12425]"}, {"versioned_ensembl_gene_id":"ENSG00000079150.17","gene_symbol":"FKBP7","gene_name":"FK506 binding protein 7 [Source:HGNC Symbol;Acc:HGNC:3723]","synonyms":"FKBP23","biotype":"protein_coding","ncbi_id":"51661","summary":"The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. Members of this family exhibit PPIase activity and function as molecular chaperones. A similar protein in mouse is located in the endoplasmic reticulum and binds calcium. [provided by RefSeq, Jul 2008]","start":178463664,"end":178478600,"strand":-1,"description":"FK506 binding protein 7 [Source:HGNC Symbol;Acc:HGNC:3723]"}, {"versioned_ensembl_gene_id":"ENSG00000253368.3","gene_symbol":"TRNP1","gene_name":"TMF1-regulated nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:34348]","synonyms":"LOC388610,C1orf225","biotype":"protein_coding","ncbi_id":"388610","summary":null,"start":26993707,"end":27000898,"strand":1,"description":"TMF1-regulated nuclear protein 1 [Source:HGNC Symbol;Acc:HGNC:34348]"}, {"versioned_ensembl_gene_id":"ENSG00000275122.4","gene_symbol":"THEMIS","gene_name":"thymocyte selection associated [Source:HGNC Symbol;Acc:HGNC:21569]","synonyms":"TSEPA,FLJ40584,C6orf207,C6orf190,bA325O24.4,bA325O24.3","biotype":"protein_coding","ncbi_id":"387357","summary":"This gene encodes a protein that plays a regulatory role in both positive and negative T-cell selection during late thymocyte development. The protein functions through T-cell antigen receptor signaling, and is necessary for proper lineage commitment and maturation of T-cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":127708072,"end":127918597,"strand":-1,"description":"thymocyte selection associated [Source:HGNC Symbol;Acc:HGNC:21569]"}, {"versioned_ensembl_gene_id":"ENSG00000105989.8","gene_symbol":"WNT2","gene_name":"Wnt family member 2 [Source:HGNC Symbol;Acc:HGNC:12780]","synonyms":"IRP,INT1L1","biotype":"protein_coding","ncbi_id":"7472","summary":"This gene is a member of the WNT gene family. The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]","start":117276631,"end":117323289,"strand":-1,"description":"Wnt family member 2 [Source:HGNC Symbol;Acc:HGNC:12780]"}, {"versioned_ensembl_gene_id":"ENSG00000136197.12","gene_symbol":"C7orf25","gene_name":"chromosome 7 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:21703]","synonyms":"MGC2821","biotype":"protein_coding","ncbi_id":"79020","summary":null,"start":42908726,"end":42912305,"strand":-1,"description":"chromosome 7 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:21703]"}, {"versioned_ensembl_gene_id":"ENSG00000235915.8","gene_symbol":"LST1","gene_name":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]","synonyms":"D6S49E,B144,LST-1","biotype":"protein_coding","ncbi_id":"7940","summary":"The protein encoded by this gene is a membrane protein that can inhibit the proliferation of lymphocytes. Expression of this gene is enhanced by lipopolysaccharide, interferon-gamma, and bacteria. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":31653110,"end":31655895,"strand":1,"description":"leukocyte specific transcript 1 [Source:HGNC Symbol;Acc:HGNC:14189]"}, {"versioned_ensembl_gene_id":"ENSG00000281841.1","gene_symbol":"AL035470.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127909833,"end":127910052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107018.7","gene_symbol":"RLN1","gene_name":"relaxin 1 [Source:HGNC Symbol;Acc:HGNC:10026]","synonyms":"H1","biotype":"protein_coding","ncbi_id":"6013","summary":"Relaxins are known endocrine and autocrine/paracrine hormones, belonging to the insulin gene superfamily. In humans there are three non-allelic relaxin genes, RLN1, RLN2 and RLN3, where RLN1 and RLN2 share high sequence homology. The protein encoded by this gene is synthesized as a single-chain polypeptide but the active form consists of an A chain and a B chain linked by disulfide bonds. Relaxin is produced by the ovary, and targets the mammalian reproductive system to ripen the cervix, elongate the pubic symphysis and inhibit uterine contraction. It may have additional roles in enhancing sperm motility, regulating blood pressure, controlling heart rate and releasing oxytocin and vasopressin. [provided by RefSeq, Jan 2013]","start":5334969,"end":5339873,"strand":-1,"description":"relaxin 1 [Source:HGNC Symbol;Acc:HGNC:10026]"}, {"versioned_ensembl_gene_id":"ENSG00000235916.1","gene_symbol":"AC233279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53825887,"end":53826309,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260308.1","gene_symbol":"AC136428.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33771035,"end":33771248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234983.1","gene_symbol":"AC010132.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42918741,"end":42920084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270467.1","gene_symbol":"IGHV3OR16-12","gene_name":"immunoglobulin heavy variable 3/OR16-12 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5636]","synonyms":"IGHV3/OR16-12","biotype":"IG_V_gene","ncbi_id":"28304","summary":null,"start":33802764,"end":33803217,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-12 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5636]"}, {"versioned_ensembl_gene_id":"ENSG00000147364.16","gene_symbol":"FBXO25","gene_name":"F-box protein 25 [Source:HGNC Symbol;Acc:HGNC:13596]","synonyms":"FBX25","biotype":"protein_coding","ncbi_id":"26260","summary":"This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":406428,"end":477967,"strand":1,"description":"F-box protein 25 [Source:HGNC Symbol;Acc:HGNC:13596]"}, {"versioned_ensembl_gene_id":"ENSG00000106588.10","gene_symbol":"PSMA2","gene_name":"proteasome subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9531]","synonyms":"MU,HC3,PMSA2","biotype":"protein_coding","ncbi_id":"5683","summary":"The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the peptidase T1A family, that is a 20S core alpha subunit. [provided by RefSeq, Jul 2008]","start":42916857,"end":42932223,"strand":-1,"description":"proteasome subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:9531]"}, {"versioned_ensembl_gene_id":"ENSG00000232523.1","gene_symbol":"BX248096.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30508488,"end":30511442,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248613.1","gene_symbol":"AC021146.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68900651,"end":68900910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261153.2","gene_symbol":"AC136428.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33808778,"end":33810767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271178.1","gene_symbol":"IGHV3OR16-13","gene_name":"immunoglobulin heavy variable 3/OR16-13 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5637]","synonyms":"IGHV3/OR16-13","biotype":"IG_V_gene","ncbi_id":"100287372","summary":null,"start":33827214,"end":33827661,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-13 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5637]"}, {"versioned_ensembl_gene_id":"ENSG00000172936.12","gene_symbol":"MYD88","gene_name":"myeloid differentiation primary response 88 [Source:HGNC Symbol;Acc:HGNC:7562]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4615","summary":"This gene encodes a cytosolic adapter protein that plays a central role in the innate and adaptive immune response. This protein functions as an essential signal transducer in the interleukin-1 and Toll-like receptor signaling pathways. These pathways regulate that activation of numerous proinflammatory genes. The encoded protein consists of an N-terminal death domain and a C-terminal Toll-interleukin1 receptor domain. Patients with defects in this gene have an increased susceptibility to pyogenic bacterial infections. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","start":38138478,"end":38143022,"strand":1,"description":"myeloid differentiation primary response 88 [Source:HGNC Symbol;Acc:HGNC:7562]"}, {"versioned_ensembl_gene_id":"ENSG00000277287.1","gene_symbol":"AL109976.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3239705,"end":3245382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242440.1","gene_symbol":"LINC02046","gene_name":"long intergenic non-protein coding RNA 2046 [Source:HGNC Symbol;Acc:HGNC:52886]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374149","summary":null,"start":148280891,"end":148399956,"strand":1,"description":"long intergenic non-protein coding RNA 2046 [Source:HGNC Symbol;Acc:HGNC:52886]"}, {"versioned_ensembl_gene_id":"ENSG00000241993.1","gene_symbol":"RPL38P1","gene_name":"ribosomal protein L38 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17093]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"116809","summary":null,"start":148695994,"end":148696204,"strand":-1,"description":"ribosomal protein L38 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17093]"}, {"versioned_ensembl_gene_id":"ENSG00000163512.13","gene_symbol":"AZI2","gene_name":"5-azacytidine induced 2 [Source:HGNC Symbol;Acc:HGNC:24002]","synonyms":"FLJ21939,AZ2,NAP1","biotype":"protein_coding","ncbi_id":"64343","summary":"AZI2, or NAP1, contributes to the activation of NFKB (see MIM 164011)-dependent gene expression by activating IKK-related kinases, such as NAK (TBK1; MIM 604834) (Fujita et al., 2003 [PubMed 14560022]).[supplied by OMIM, Mar 2008]","start":28315003,"end":28349127,"strand":-1,"description":"5-azacytidine induced 2 [Source:HGNC Symbol;Acc:HGNC:24002]"}, {"versioned_ensembl_gene_id":"ENSG00000135333.13","gene_symbol":"EPHA7","gene_name":"EPH receptor A7 [Source:HGNC Symbol;Acc:HGNC:3390]","synonyms":"Hek11","biotype":"protein_coding","ncbi_id":"2045","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Increased expression of this gene is associated with multiple forms of carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":93240020,"end":93419547,"strand":-1,"description":"EPH receptor A7 [Source:HGNC Symbol;Acc:HGNC:3390]"}, {"versioned_ensembl_gene_id":"ENSG00000233795.6","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"hZR14,tctex-6,RPA12,HTEX-6","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30049286,"end":30055293,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000284522.1","gene_symbol":"AC006927.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7626103,"end":7626486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272626.1","gene_symbol":"AC021146.12","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":68901008,"end":68906983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259445.1","gene_symbol":"AC025219.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81953303,"end":81995666,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224739.2","gene_symbol":"AC016735.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43001355,"end":43006060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111696.11","gene_symbol":"NT5DC3","gene_name":"5'-nucleotidase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30826]","synonyms":"TU12B1-TY,FLJ11266","biotype":"protein_coding","ncbi_id":"51559","summary":null,"start":103770453,"end":103841197,"strand":-1,"description":"5'-nucleotidase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:30826]"}, {"versioned_ensembl_gene_id":"ENSG00000197121.14","gene_symbol":"PGAP1","gene_name":"post-GPI attachment to proteins 1 [Source:HGNC Symbol;Acc:HGNC:25712]","synonyms":"SPG67,FLJ12377,Bst1","biotype":"protein_coding","ncbi_id":"80055","summary":"The protein encoded by this gene functions early in the glycosylphosphatidylinositol (GPI) biosynthetic pathway, catalyzing the inositol deacylation of GPI. The encoded protein is required for the production of GPI that can attach to proteins, and this may be an important factor in the transport of GPI-anchored proteins from the endoplasmic reticulum to the Golgi. Defects in this gene are a cause an autosomal recessive form of cognitive impairment. [provided by RefSeq, Jul 2017]","start":196833004,"end":196927796,"strand":-1,"description":"post-GPI attachment to proteins 1 [Source:HGNC Symbol;Acc:HGNC:25712]"}, {"versioned_ensembl_gene_id":"ENSG00000231826.5","gene_symbol":"LINC01819","gene_name":"long intergenic non-protein coding RNA 1819 [Source:HGNC Symbol;Acc:HGNC:52624]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102723854","summary":null,"start":43027853,"end":43039547,"strand":-1,"description":"long intergenic non-protein coding RNA 1819 [Source:HGNC Symbol;Acc:HGNC:52624]"}, {"versioned_ensembl_gene_id":"ENSG00000249985.1","gene_symbol":"AC021146.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68907918,"end":68908034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198277.6","gene_symbol":"AC021146.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68914928,"end":68924741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238202.1","gene_symbol":"AC002465.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117300861,"end":117322236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270711.1","gene_symbol":"AL162431.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":180970837,"end":180971247,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232586.1","gene_symbol":"KIAA1614-AS1","gene_name":"KIAA1614 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50644]","synonyms":"RP11-46A10.4","biotype":"antisense_RNA","ncbi_id":"103344928","summary":null,"start":180949699,"end":180954887,"strand":-1,"description":"KIAA1614 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50644]"}, {"versioned_ensembl_gene_id":"ENSG00000251520.1","gene_symbol":"AL162431.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":180964511,"end":180965909,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111701.6","gene_symbol":"APOBEC1","gene_name":"apolipoprotein B mRNA editing enzyme catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:604]","synonyms":"BEDP,APOBEC-1,HEPR,CDAR1","biotype":"protein_coding","ncbi_id":"339","summary":"This gene encodes a member of the cytidine deaminase enzyme family. The encoded protein forms a multiple-protein editing holoenzyme with APOBEC1 complementation factor (ACF) and APOBEC1 stimulating protein (ASP). This holoenzyme is involved in the editing of C-to-U nucleotide bases in apolipoprotein B and neurofibromatosis-1 mRNAs. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2015]","start":7649400,"end":7665903,"strand":-1,"description":"apolipoprotein B mRNA editing enzyme catalytic subunit 1 [Source:HGNC Symbol;Acc:HGNC:604]"}, {"versioned_ensembl_gene_id":"ENSG00000262480.2","gene_symbol":"SAMD11P1","gene_name":"sterile alpha motif domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44473]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421331","summary":null,"start":2613284,"end":2613944,"strand":-1,"description":"sterile alpha motif domain containing 11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44473]"}, {"versioned_ensembl_gene_id":"ENSG00000279432.1","gene_symbol":"AC015799.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2639297,"end":2642418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242361.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32987867,"end":32992379,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000259622.1","gene_symbol":"AC026956.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82010212,"end":82010607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135823.13","gene_symbol":"STX6","gene_name":"syntaxin 6 [Source:HGNC Symbol;Acc:HGNC:11441]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10228","summary":null,"start":180972712,"end":181023121,"strand":-1,"description":"syntaxin 6 [Source:HGNC Symbol;Acc:HGNC:11441]"}, {"versioned_ensembl_gene_id":"ENSG00000230864.1","gene_symbol":"AC099567.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":102763322,"end":102853842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243802.2","gene_symbol":"AC090589.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47191181,"end":47191542,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255850.1","gene_symbol":"TMEM5-AS1","gene_name":"TMEM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48910]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104169670","summary":null,"start":63808845,"end":63822156,"strand":-1,"description":"TMEM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48910]"}, {"versioned_ensembl_gene_id":"ENSG00000219669.1","gene_symbol":"BECN1P2","gene_name":"beclin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51330]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420149","summary":null,"start":71075564,"end":71076375,"strand":1,"description":"beclin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51330]"}, {"versioned_ensembl_gene_id":"ENSG00000153214.9","gene_symbol":"TMEM87B","gene_name":"transmembrane protein 87B [Source:HGNC Symbol;Acc:HGNC:25913]","synonyms":"FLJ14681","biotype":"protein_coding","ncbi_id":"84910","summary":"This gene encodes a protein that may interact with human papillomavirus type 18 E6 oncogene. The protein is also likely to be involved in endosome-to-trans-Golgi network retrograde transport. The gene is expressed in adult and fetal tissues, including brain and heart. This gene is a component of the 2q13 deletion syndrome. Mutations in this gene may be associated with congenital heart defects. [provided by RefSeq, Aug 2016]","start":112055223,"end":112119318,"strand":1,"description":"transmembrane protein 87B [Source:HGNC Symbol;Acc:HGNC:25913]"}, {"versioned_ensembl_gene_id":"ENSG00000229701.1","gene_symbol":"MTND2P20","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42121]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873226","summary":null,"start":155264163,"end":155264823,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:42121]"}, {"versioned_ensembl_gene_id":"ENSG00000118600.11","gene_symbol":"TMEM5","gene_name":"transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:13530]","synonyms":"HP10481","biotype":"protein_coding","ncbi_id":"10329","summary":"This gene encodes a type II transmembrane protein that is thought to have glycosyltransferase function. Mutations in this gene result in cobblestone lissencephaly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":63779803,"end":63809558,"strand":1,"description":"transmembrane protein 5 [Source:HGNC Symbol;Acc:HGNC:13530]"}, {"versioned_ensembl_gene_id":"ENSG00000218350.1","gene_symbol":"LYPLA1P3","gene_name":"lysophospholipase I pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44007]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"157713","summary":null,"start":71165076,"end":71165770,"strand":1,"description":"lysophospholipase I pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44007]"}, {"versioned_ensembl_gene_id":"ENSG00000169800.13","gene_symbol":"RBMY1F","gene_name":"RNA binding motif protein, Y-linked, family 1, member F [Source:HGNC Symbol;Acc:HGNC:23974]","synonyms":"MGC33094","biotype":"protein_coding","ncbi_id":"159163","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. Multiple copies of this gene are found in the AZFb azoospermia factor region of chromosome Y and the encoded protein is thought to be involved in spermatogenesis. Most copies of this locus are pseudogenes, although six highly similar copies have full-length ORFs and are considered functional. Four functional copies of this gene are found within inverted repeat IR2; two functional copies of this gene are found in palindrome P3, along with two copies of PTPN13-like, Y-linked. [provided by RefSeq, Jul 2008]","start":22168542,"end":22182982,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 1, member F [Source:HGNC Symbol;Acc:HGNC:23974]"}, {"versioned_ensembl_gene_id":"ENSG00000148734.7","gene_symbol":"NPFFR1","gene_name":"neuropeptide FF receptor 1 [Source:HGNC Symbol;Acc:HGNC:17425]","synonyms":"GPR147,OT7T022,NPFF1R1","biotype":"protein_coding","ncbi_id":"64106","summary":null,"start":70247329,"end":70283676,"strand":-1,"description":"neuropeptide FF receptor 1 [Source:HGNC Symbol;Acc:HGNC:17425]"}, {"versioned_ensembl_gene_id":"ENSG00000227682.2","gene_symbol":"ATP5A1P2","gene_name":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:828]","synonyms":"ATP5AP2","biotype":"transcribed_processed_pseudogene","ncbi_id":"504","summary":null,"start":155269633,"end":155270134,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:828]"}, {"versioned_ensembl_gene_id":"ENSG00000233709.1","gene_symbol":"MTND4P28","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42215]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873249","summary":null,"start":155311023,"end":155311409,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:42215]"}, {"versioned_ensembl_gene_id":"ENSG00000257754.1","gene_symbol":"AC012555.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103819610,"end":103822085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233039.1","gene_symbol":"MTND5P30","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42292]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873266","summary":null,"start":155311697,"end":155313427,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:42292]"}, {"versioned_ensembl_gene_id":"ENSG00000233248.1","gene_symbol":"MTND6P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39472]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478946","summary":null,"start":155313440,"end":155313958,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:39472]"}, {"versioned_ensembl_gene_id":"ENSG00000169550.12","gene_symbol":"MUC15","gene_name":"mucin 15, cell surface associated [Source:HGNC Symbol;Acc:HGNC:14956]","synonyms":null,"biotype":"protein_coding","ncbi_id":"143662","summary":null,"start":26559033,"end":26572233,"strand":-1,"description":"mucin 15, cell surface associated [Source:HGNC Symbol;Acc:HGNC:14956]"}, {"versioned_ensembl_gene_id":"ENSG00000229935.1","gene_symbol":"MTCYBP9","gene_name":"mitochondrially encoded cytochrome b pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51966]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075124","summary":null,"start":155314066,"end":155314368,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:51966]"}, {"versioned_ensembl_gene_id":"ENSG00000183496.5","gene_symbol":"MEX3B","gene_name":"mex-3 RNA binding family member B [Source:HGNC Symbol;Acc:HGNC:25297]","synonyms":"RNF195,RKHD3,DKFZp434J0617","biotype":"protein_coding","ncbi_id":"84206","summary":"This gene encodes an RNA-binding phosphoprotein that is part of the MEX3 (muscle excess 3) family of translational regulators. The encoded protein contains N-terminal nuclear export and nuclear localization signals and is exported from the cytoplasm to the nucleus. The protein binds to RNA via two KH domains and also colocalizes with MEX3A, Dcp1A decapping factor and Argonaute proteins within P (processing) bodies. [provided by RefSeq, Oct 2012]","start":82041778,"end":82046141,"strand":-1,"description":"mex-3 RNA binding family member B [Source:HGNC Symbol;Acc:HGNC:25297]"}, {"versioned_ensembl_gene_id":"ENSG00000226383.6","gene_symbol":"LINC01876","gene_name":"long intergenic non-protein coding RNA 1876 [Source:HGNC Symbol;Acc:HGNC:52695]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929378","summary":null,"start":156011530,"end":156254950,"strand":-1,"description":"long intergenic non-protein coding RNA 1876 [Source:HGNC Symbol;Acc:HGNC:52695]"}, {"versioned_ensembl_gene_id":"ENSG00000250596.2","gene_symbol":"AC096751.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":174523701,"end":174540344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144891.17","gene_symbol":"AGTR1","gene_name":"angiotensin II receptor type 1 [Source:HGNC Symbol;Acc:HGNC:336]","synonyms":"AT2R1A,AT2R1,AT1B,AT1,AGTR1B,AGTR1A,AG2S,HAT1R,AT2R1B","biotype":"protein_coding","ncbi_id":"185","summary":"Angiotensin II is a potent vasopressor hormone and a primary regulator of aldosterone secretion. It is an important effector controlling blood pressure and volume in the cardiovascular system. It acts through at least two types of receptors. This gene encodes the type 1 receptor which is thought to mediate the major cardiovascular effects of angiotensin II. This gene may play a role in the generation of reperfusion arrhythmias following restoration of blood flow to ischemic or infarcted myocardium. It was previously thought that a related gene, denoted as AGTR1B, existed; however, it is now believed that there is only one type 1 receptor gene in humans. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2020]","start":148697784,"end":148743008,"strand":1,"description":"angiotensin II receptor type 1 [Source:HGNC Symbol;Acc:HGNC:336]"}, {"versioned_ensembl_gene_id":"ENSG00000251584.1","gene_symbol":"AC096751.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":174536640,"end":174540784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138363.14","gene_symbol":"ATIC","gene_name":"5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase [Source:HGNC Symbol;Acc:HGNC:794]","synonyms":"IMPCHASE,AICARFT,PURH","biotype":"protein_coding","ncbi_id":"471","summary":"This gene encodes a bifunctional protein that catalyzes the last two steps of the de novo purine biosynthetic pathway. The N-terminal domain has phosphoribosylaminoimidazolecarboxamide formyltransferase activity, and the C-terminal domain has IMP cyclohydrolase activity. A mutation in this gene results in AICA-ribosiduria. [provided by RefSeq, Sep 2009]","start":215311817,"end":215349773,"strand":1,"description":"5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase [Source:HGNC Symbol;Acc:HGNC:794]"}, {"versioned_ensembl_gene_id":"ENSG00000282124.1","gene_symbol":"AC015849.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35893707,"end":35911023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235548.1","gene_symbol":"AC073551.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":156033247,"end":156034080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261210.7","gene_symbol":"CLEC19A","gene_name":"C-type lectin domain containing 19A [Source:HGNC Symbol;Acc:HGNC:34522]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728276","summary":null,"start":19285739,"end":19322145,"strand":1,"description":"C-type lectin domain containing 19A [Source:HGNC Symbol;Acc:HGNC:34522]"}, {"versioned_ensembl_gene_id":"ENSG00000175727.13","gene_symbol":"MLXIP","gene_name":"MLX interacting protein [Source:HGNC Symbol;Acc:HGNC:17055]","synonyms":"KIAA0867,bHLHe36,MONDOA,MIR","biotype":"protein_coding","ncbi_id":"22877","summary":"This gene encodes a protein that functions as part of a heterodimer to activate transcription. The encoded protein forms a heterodimer with Max-like protein X (MLX) and is involved in the regulation of genes in response to cellular glucose levels. [provided by RefSeq, Mar 2014]","start":122078722,"end":122147347,"strand":1,"description":"MLX interacting protein [Source:HGNC Symbol;Acc:HGNC:17055]"}, {"versioned_ensembl_gene_id":"ENSG00000214190.2","gene_symbol":"RNF152P1","gene_name":"ring finger protein 152 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49743]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419687","summary":null,"start":5418373,"end":5418976,"strand":-1,"description":"ring finger protein 152 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49743]"}, {"versioned_ensembl_gene_id":"ENSG00000106628.10","gene_symbol":"POLD2","gene_name":"DNA polymerase delta 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9176]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5425","summary":"This gene encodes the 50-kDa catalytic subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. The encoded protein is required for the stimulation of DNA polymerase delta activity by the processivity cofactor proliferating cell nuclear antigen (PCNA). Expression of this gene may be a marker for ovarian carcinomas. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Mar 2012]","start":44114681,"end":44124358,"strand":-1,"description":"DNA polymerase delta 2, accessory subunit [Source:HGNC Symbol;Acc:HGNC:9176]"}, {"versioned_ensembl_gene_id":"ENSG00000134343.12","gene_symbol":"ANO3","gene_name":"anoctamin 3 [Source:HGNC Symbol;Acc:HGNC:14004]","synonyms":"DYT23,C11orf25,TMEM16C,GENX-3947","biotype":"protein_coding","ncbi_id":"63982","summary":"The protein encoded by this gene belongs to the TMEM16 family of predicted membrane proteins, that are also known as anoctamins. While little is known about the function of this gene, mutations in this gene have been associated with some cases of autosomal dominant craniocervical dystonia. Cells from individuals with a mutation in this gene exhibited abnormalities in endoplasmic reticulum-dependent calcium signaling. Studies in rat show that the rat ortholog of this protein interacts with, and modulates the activity of a sodium-activated potassium channel. Deletion of this gene caused increased pain sensitivity in the rat model system. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]","start":26309599,"end":26663288,"strand":1,"description":"anoctamin 3 [Source:HGNC Symbol;Acc:HGNC:14004]"}, {"versioned_ensembl_gene_id":"ENSG00000135835.11","gene_symbol":"KIAA1614","gene_name":"KIAA1614 [Source:HGNC Symbol;Acc:HGNC:29327]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57710","summary":null,"start":180913154,"end":180951614,"strand":1,"description":"KIAA1614 [Source:HGNC Symbol;Acc:HGNC:29327]"}, {"versioned_ensembl_gene_id":"ENSG00000233983.2","gene_symbol":"AL365220.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99464378,"end":99464776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224445.3","gene_symbol":"LINC01708","gene_name":"long intergenic non-protein coding RNA 1708 [Source:HGNC Symbol;Acc:HGNC:52496]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928270","summary":null,"start":99472332,"end":99600995,"strand":-1,"description":"long intergenic non-protein coding RNA 1708 [Source:HGNC Symbol;Acc:HGNC:52496]"}, {"versioned_ensembl_gene_id":"ENSG00000186009.4","gene_symbol":"ATP4B","gene_name":"ATPase H+/K+ transporting beta subunit [Source:HGNC Symbol;Acc:HGNC:820]","synonyms":"ATP6B","biotype":"protein_coding","ncbi_id":"496","summary":"The protein encoded by this gene belongs to a family of P-type cation-transporting ATPases. The gastric H+, K+-ATPase is a heterodimer consisting of a high molecular weight catalytic alpha subunit and a smaller but heavily glycosylated beta subunit. This enzyme is a proton pump that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for gastric acid secretion. This gene encodes the beta subunit of the gastric H+, K+-ATPase. [provided by RefSeq, Jul 2008]","start":113648804,"end":113658186,"strand":-1,"description":"ATPase H+/K+ transporting beta subunit [Source:HGNC Symbol;Acc:HGNC:820]"}, {"versioned_ensembl_gene_id":"ENSG00000259871.1","gene_symbol":"AC130456.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19315164,"end":19316526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280265.1","gene_symbol":"AC130456.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":19392213,"end":19393468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259925.1","gene_symbol":"AC130456.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19343647,"end":19401693,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184363.9","gene_symbol":"PKP3","gene_name":"plakophilin 3 [Source:HGNC Symbol;Acc:HGNC:9025]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11187","summary":"This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may act in cellular desmosome-dependent adhesion and signaling pathways. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]","start":392614,"end":404908,"strand":1,"description":"plakophilin 3 [Source:HGNC Symbol;Acc:HGNC:9025]"}, {"versioned_ensembl_gene_id":"ENSG00000282440.1","gene_symbol":"AC074099.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":156305108,"end":156320255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272866.1","gene_symbol":"AL135786.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5351796,"end":5352410,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242092.8","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32973881,"end":32992379,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000231967.1","gene_symbol":"AL135786.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5356312,"end":5356525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240027.2","gene_symbol":"AC084357.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63760358,"end":63760612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243155.1","gene_symbol":"AL162431.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":180944042,"end":180976482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230012.1","gene_symbol":"HTATSF1P1","gene_name":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]","synonyms":"HTATSF1P,dJ1033B10.6,TAT-SF1-L","biotype":"processed_pseudogene","ncbi_id":"387039","summary":null,"start":33391691,"end":33393582,"strand":1,"description":"HIV-1 Tat specific factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13959]"}, {"versioned_ensembl_gene_id":"ENSG00000151067.21","gene_symbol":"CACNA1C","gene_name":"calcium voltage-gated channel subunit alpha1 C [Source:HGNC Symbol;Acc:HGNC:1390]","synonyms":"LQT8,CCHL1A1,Cav1.2,CACNL1A1,CACN2,CACH2,TS","biotype":"protein_coding","ncbi_id":"775","summary":"This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. Some of the predicted proteins may not produce functional ion channel subunits. [provided by RefSeq, Oct 2012]","start":1970786,"end":2697950,"strand":1,"description":"calcium voltage-gated channel subunit alpha1 C [Source:HGNC Symbol;Acc:HGNC:1390]"}, {"versioned_ensembl_gene_id":"ENSG00000217241.1","gene_symbol":"CBX3P9","gene_name":"chromobox 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42881]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644101","summary":null,"start":116453014,"end":116453565,"strand":-1,"description":"chromobox 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42881]"}, {"versioned_ensembl_gene_id":"ENSG00000242261.1","gene_symbol":"AC018635.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128306649,"end":128307678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162601.9","gene_symbol":"MYSM1","gene_name":"Myb like, SWIRM and MPN domains 1 [Source:HGNC Symbol;Acc:HGNC:29401]","synonyms":"KIAA1915","biotype":"protein_coding","ncbi_id":"114803","summary":null,"start":58654739,"end":58700092,"strand":-1,"description":"Myb like, SWIRM and MPN domains 1 [Source:HGNC Symbol;Acc:HGNC:29401]"}, {"versioned_ensembl_gene_id":"ENSG00000107020.9","gene_symbol":"PLGRKT","gene_name":"plasminogen receptor with a C-terminal lysine [Source:HGNC Symbol;Acc:HGNC:23633]","synonyms":"Plg-RKT,MDS030,FLJ14688,C9orf46,AD025","biotype":"protein_coding","ncbi_id":"55848","summary":null,"start":5357973,"end":5437878,"strand":-1,"description":"plasminogen receptor with a C-terminal lysine [Source:HGNC Symbol;Acc:HGNC:23633]"}, {"versioned_ensembl_gene_id":"ENSG00000237137.1","gene_symbol":"AL159169.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":14531916,"end":14532042,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106344.8","gene_symbol":"RBM28","gene_name":"RNA binding motif protein 28 [Source:HGNC Symbol;Acc:HGNC:21863]","synonyms":"FLJ10377","biotype":"protein_coding","ncbi_id":"55131","summary":"The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":128297685,"end":128343908,"strand":-1,"description":"RNA binding motif protein 28 [Source:HGNC Symbol;Acc:HGNC:21863]"}, {"versioned_ensembl_gene_id":"ENSG00000260577.2","gene_symbol":"AC126773.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68644248,"end":68646168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184792.15","gene_symbol":"OSBP2","gene_name":"oxysterol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8504]","synonyms":"OSBPL1,ORP4,ORP-4,KIAA1664","biotype":"protein_coding","ncbi_id":"23762","summary":"The protein encoded by this gene contains a pleckstrin homology (PH) domain and an oxysterol-binding region. It binds oxysterols such as 7-ketocholesterol and may inhibit their cytotoxicity. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2013]","start":30693782,"end":30907824,"strand":1,"description":"oxysterol binding protein 2 [Source:HGNC Symbol;Acc:HGNC:8504]"}, {"versioned_ensembl_gene_id":"ENSG00000260860.2","gene_symbol":"AC126773.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68651056,"end":68651948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261395.3","gene_symbol":"HSPE1P5","gene_name":"heat shock protein family E (Hsp10) member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49324]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100506000","summary":null,"start":68686399,"end":68686670,"strand":1,"description":"heat shock protein family E (Hsp10) member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:49324]"}, {"versioned_ensembl_gene_id":"ENSG00000062038.13","gene_symbol":"CDH3","gene_name":"cadherin 3 [Source:HGNC Symbol;Acc:HGNC:1762]","synonyms":"PCAD,CDHP","biotype":"protein_coding","ncbi_id":"1001","summary":"This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas. Mutations in this gene are associated with hypotrichosis with juvenile macular dystrophy and ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome (EEMS). [provided by RefSeq, Nov 2015]","start":68636189,"end":68722616,"strand":1,"description":"cadherin 3 [Source:HGNC Symbol;Acc:HGNC:1762]"}, {"versioned_ensembl_gene_id":"ENSG00000214050.7","gene_symbol":"FBXO16","gene_name":"F-box protein 16 [Source:HGNC Symbol;Acc:HGNC:13618]","synonyms":"FBX16","biotype":"protein_coding","ncbi_id":"157574","summary":"This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into three classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbx class. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":28348287,"end":28490318,"strand":-1,"description":"F-box protein 16 [Source:HGNC Symbol;Acc:HGNC:13618]"}, {"versioned_ensembl_gene_id":"ENSG00000271639.1","gene_symbol":"AC019072.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":233545482,"end":233547032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000085982.13","gene_symbol":"USP40","gene_name":"ubiquitin specific peptidase 40 [Source:HGNC Symbol;Acc:HGNC:20069]","synonyms":"FLJ10785","biotype":"protein_coding","ncbi_id":"55230","summary":"Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP40 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Mar 2008]","start":233475520,"end":233566782,"strand":-1,"description":"ubiquitin specific peptidase 40 [Source:HGNC Symbol;Acc:HGNC:20069]"}, {"versioned_ensembl_gene_id":"ENSG00000162614.18","gene_symbol":"NEXN","gene_name":"nexilin F-actin binding protein [Source:HGNC Symbol;Acc:HGNC:29557]","synonyms":"nexilin,NELIN","biotype":"protein_coding","ncbi_id":"91624","summary":"This gene encodes a filamentous actin-binding protein that may function in cell adhesion and migration. Mutations in this gene have been associated with dilated cardiomyopathy, also known as CMD1CC. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]","start":77888513,"end":77943895,"strand":1,"description":"nexilin F-actin binding protein [Source:HGNC Symbol;Acc:HGNC:29557]"}, {"versioned_ensembl_gene_id":"ENSG00000229034.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29983708,"end":29984585,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000235309.7","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"D6S203,HLA-CDA12,CDA12,HLA-59","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":29995855,"end":29999228,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000227017.1","gene_symbol":"AC007036.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30176387,"end":30179014,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237441.9","gene_symbol":"RGL2","gene_name":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]","synonyms":"KE1.5,HKE1.5,RAB2L","biotype":"protein_coding","ncbi_id":"5863","summary":null,"start":33291654,"end":33299324,"strand":-1,"description":"ral guanine nucleotide dissociation stimulator like 2 [Source:HGNC Symbol;Acc:HGNC:9769]"}, {"versioned_ensembl_gene_id":"ENSG00000099260.10","gene_symbol":"PALMD","gene_name":"palmdelphin [Source:HGNC Symbol;Acc:HGNC:15846]","synonyms":"PALML,FLJ20271,C1orf11","biotype":"protein_coding","ncbi_id":"54873","summary":null,"start":99645943,"end":99694541,"strand":1,"description":"palmdelphin [Source:HGNC Symbol;Acc:HGNC:15846]"}, {"versioned_ensembl_gene_id":"ENSG00000281404.1","gene_symbol":"LINC01176","gene_name":"long intergenic non-protein coding RNA 1176 [Source:NCBI gene;Acc:100506516]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506516","summary":null,"start":30390885,"end":30412375,"strand":1,"description":"long intergenic non-protein coding RNA 1176 [Source:NCBI gene;Acc:100506516]"}, {"versioned_ensembl_gene_id":"ENSG00000235380.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29960061,"end":29961724,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000235305.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BAT1P2,BPG309N1.15","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29982480,"end":29982876,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000180233.10","gene_symbol":"ZNRF2","gene_name":"zinc and ring finger 2 [Source:HGNC Symbol;Acc:HGNC:22316]","synonyms":"RNF202","biotype":"protein_coding","ncbi_id":"223082","summary":null,"start":30284307,"end":30367692,"strand":1,"description":"zinc and ring finger 2 [Source:HGNC Symbol;Acc:HGNC:22316]"}, {"versioned_ensembl_gene_id":"ENSG00000223996.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30022074,"end":30023364,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000234786.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29945879,"end":29947844,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000223980.10","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29930538,"end":29999232,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000100320.22","gene_symbol":"RBFOX2","gene_name":"RNA binding protein, fox-1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:9906]","synonyms":"RBM9,HRNBP2,HNRBP2,FOX-2","biotype":"protein_coding","ncbi_id":"23543","summary":"This gene is one of several human genes similar to the C. elegans gene Fox-1. This gene encodes an RNA binding protein that is thought to be a key regulator of alternative exon splicing in the nervous system and other cell types. The protein binds to a conserved UGCAUG element found downstream of many alternatively spliced exons and promotes inclusion of the alternative exon in mature transcripts. The protein also interacts with the estrogen receptor 1 transcription factor and regulates estrogen receptor 1 transcriptional activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":35738736,"end":36028425,"strand":-1,"description":"RNA binding protein, fox-1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:9906]"}, {"versioned_ensembl_gene_id":"ENSG00000271933.1","gene_symbol":"AL603756.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":84138420,"end":84140582,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235859.5","gene_symbol":"AC006978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30371508,"end":30372741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165678.20","gene_symbol":"GHITM","gene_name":"growth hormone inducible transmembrane protein [Source:HGNC Symbol;Acc:HGNC:17281]","synonyms":"HSPC282,DERP2,TMBIM5,PTD010,My021","biotype":"protein_coding","ncbi_id":"27069","summary":null,"start":84139440,"end":84153245,"strand":1,"description":"growth hormone inducible transmembrane protein [Source:HGNC Symbol;Acc:HGNC:17281]"}, {"versioned_ensembl_gene_id":"ENSG00000106635.7","gene_symbol":"BCL7B","gene_name":"BCL tumor suppressor 7B [Source:HGNC Symbol;Acc:HGNC:1005]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9275","summary":"This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2010]","start":73536356,"end":73558002,"strand":-1,"description":"BCL tumor suppressor 7B [Source:HGNC Symbol;Acc:HGNC:1005]"}, {"versioned_ensembl_gene_id":"ENSG00000188266.13","gene_symbol":"HYKK","gene_name":"hydroxylysine kinase [Source:HGNC Symbol;Acc:HGNC:34403]","synonyms":"LOC123688,AGPHD1","biotype":"protein_coding","ncbi_id":"123688","summary":null,"start":78507564,"end":78537372,"strand":1,"description":"hydroxylysine kinase [Source:HGNC Symbol;Acc:HGNC:34403]"}, {"versioned_ensembl_gene_id":"ENSG00000234257.1","gene_symbol":"SOD2P1","gene_name":"superoxide dismutase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45268]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421046","summary":null,"start":103100143,"end":103100704,"strand":-1,"description":"superoxide dismutase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45268]"}, {"versioned_ensembl_gene_id":"ENSG00000259680.5","gene_symbol":"AC136428.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":33844784,"end":33845229,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281593.1","gene_symbol":"AC006978.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30362400,"end":30412502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270924.1","gene_symbol":"AC140658.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33848476,"end":33848644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115750.16","gene_symbol":"TAF1B","gene_name":"TATA-box binding protein associated factor, RNA polymerase I subunit B [Source:HGNC Symbol;Acc:HGNC:11533]","synonyms":"TAFI63,SL1,RAFI63,RAF1B","biotype":"protein_coding","ncbi_id":"9014","summary":"Initiation of transcription by RNA polymerase I requires the formation of a complex composed of the TATA-binding protein (TBP) and three TBP-associated factors (TAFs) specific for RNA polymerase I. This complex, known as SL1, binds to the core promoter of ribosomal RNA genes to position the polymerase properly and acts as a channel for regulatory signals. This gene encodes one of the SL1-specific TAFs. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]","start":9843354,"end":9934416,"strand":1,"description":"TATA-box binding protein associated factor, RNA polymerase I subunit B [Source:HGNC Symbol;Acc:HGNC:11533]"}, {"versioned_ensembl_gene_id":"ENSG00000060718.20","gene_symbol":"COL11A1","gene_name":"collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]","synonyms":"STL2,COLL6,CO11A1","biotype":"protein_coding","ncbi_id":"1301","summary":"This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome. A single-nucleotide polymorphism in this gene is also associated with susceptibility to lumbar disc herniation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]","start":102876467,"end":103108496,"strand":-1,"description":"collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]"}, {"versioned_ensembl_gene_id":"ENSG00000272293.1","gene_symbol":"AC083964.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":450714,"end":451343,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275581.4","gene_symbol":"SERF1A","gene_name":"small EDRK-rich factor 1A [Source:HGNC Symbol;Acc:HGNC:10755]","synonyms":"4F5,SMAM1,SERF1,H4F5,FAM2A","biotype":"protein_coding","ncbi_id":"8293","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The duplication region includes both a telomeric and a centromeric copy of this gene. Deletions of this gene, the telomeric copy, often accompany deletions of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients, and so it is thought that this gene may be a modifier of the SMA phenotype. The function of this protein is not known; however, it bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. [provided by RefSeq, Jul 2008]","start":70244409,"end":70262299,"strand":1,"description":"small EDRK-rich factor 1A [Source:HGNC Symbol;Acc:HGNC:10755]"}, {"versioned_ensembl_gene_id":"ENSG00000223343.1","gene_symbol":"AC137630.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48985049,"end":48989988,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178467.17","gene_symbol":"P4HTM","gene_name":"prolyl 4-hydroxylase, transmembrane [Source:HGNC Symbol;Acc:HGNC:28858]","synonyms":"PHD4,PH4,PH-4,P4H-TM,HIFPH4,FLJ20262,EGLN4","biotype":"protein_coding","ncbi_id":"54681","summary":"The product of this gene belongs to the family of prolyl 4-hydroxylases. This protein is a prolyl hydroxylase that may be involved in the degradation of hypoxia-inducible transcription factors under normoxia. It plays a role in adaptation to hypoxia and may be related to cellular oxygen sensing. Alternatively spliced variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":48989886,"end":49007154,"strand":1,"description":"prolyl 4-hydroxylase, transmembrane [Source:HGNC Symbol;Acc:HGNC:28858]"}, {"versioned_ensembl_gene_id":"ENSG00000280053.1","gene_symbol":"AC011199.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":126973065,"end":126976426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174776.10","gene_symbol":"WDR49","gene_name":"WD repeat domain 49 [Source:HGNC Symbol;Acc:HGNC:26587]","synonyms":"FLJ33620","biotype":"protein_coding","ncbi_id":"151790","summary":"This gene encodes a member of the WD repeat protein family with nine WD repeats. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":167478684,"end":167653983,"strand":-1,"description":"WD repeat domain 49 [Source:HGNC Symbol;Acc:HGNC:26587]"}, {"versioned_ensembl_gene_id":"ENSG00000258235.1","gene_symbol":"AC133480.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":72727923,"end":72728844,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172731.13","gene_symbol":"LRRC20","gene_name":"leucine rich repeat containing 20 [Source:HGNC Symbol;Acc:HGNC:23421]","synonyms":"FLJ10844,FLJ10751","biotype":"protein_coding","ncbi_id":"55222","summary":null,"start":70298970,"end":70382650,"strand":-1,"description":"leucine rich repeat containing 20 [Source:HGNC Symbol;Acc:HGNC:23421]"}, {"versioned_ensembl_gene_id":"ENSG00000279373.1","gene_symbol":"AC027228.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":78537681,"end":78538946,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253432.1","gene_symbol":"AC027541.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139096305,"end":139102830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255505.1","gene_symbol":"AC079064.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26427051,"end":26427412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185974.6","gene_symbol":"GRK1","gene_name":"G protein-coupled receptor kinase 1 [Source:HGNC Symbol;Acc:HGNC:10013]","synonyms":"RK,RHOK,GPRK1","biotype":"protein_coding","ncbi_id":"6011","summary":"This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates rhodopsin and initiates its deactivation. Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2). [provided by RefSeq, Jul 2008]","start":113667155,"end":113737735,"strand":1,"description":"G protein-coupled receptor kinase 1 [Source:HGNC Symbol;Acc:HGNC:10013]"}, {"versioned_ensembl_gene_id":"ENSG00000269489.1","gene_symbol":"AL589765.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":151798054,"end":151798602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204979.7","gene_symbol":"MS4A13","gene_name":"membrane spanning 4-domains A13 [Source:HGNC Symbol;Acc:HGNC:16674]","synonyms":null,"biotype":"protein_coding","ncbi_id":"503497","summary":null,"start":60515413,"end":60542721,"strand":1,"description":"membrane spanning 4-domains A13 [Source:HGNC Symbol;Acc:HGNC:16674]"}, {"versioned_ensembl_gene_id":"ENSG00000276139.4","gene_symbol":"KIR2DS2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]","synonyms":"183ActI,CD158J,cl-49,nkat5","biotype":"protein_coding","ncbi_id":"100132285","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":54738560,"end":54752721,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6334]"}, {"versioned_ensembl_gene_id":"ENSG00000254370.1","gene_symbol":"AC025871.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28415524,"end":28420055,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253567.1","gene_symbol":"AC025871.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28447264,"end":28455902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238173.1","gene_symbol":"RPL39P6","gene_name":"ribosomal protein L39 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270891","summary":null,"start":11232963,"end":11233112,"strand":1,"description":"ribosomal protein L39 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:35803]"}, {"versioned_ensembl_gene_id":"ENSG00000143365.17","gene_symbol":"RORC","gene_name":"RAR related orphan receptor C [Source:HGNC Symbol;Acc:HGNC:10260]","synonyms":"TOR,RZRG,RORG,NR1F3","biotype":"protein_coding","ncbi_id":"6097","summary":"The protein encoded by this gene is a DNA-binding transcription factor and is a member of the NR1 subfamily of nuclear hormone receptors. The specific functions of this protein are not known; however, studies of a similar gene in mice have shown that this gene may be essential for lymphoid organogenesis and may play an important regulatory role in thymopoiesis. In addition, studies in mice suggest that the protein encoded by this gene may inhibit the expression of Fas ligand and IL2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":151806071,"end":151831872,"strand":-1,"description":"RAR related orphan receptor C [Source:HGNC Symbol;Acc:HGNC:10260]"}, {"versioned_ensembl_gene_id":"ENSG00000186918.13","gene_symbol":"ZNF395","gene_name":"zinc finger protein 395 [Source:HGNC Symbol;Acc:HGNC:18737]","synonyms":"DKFZp434K1210,PRF-1,PBF,HDBP2","biotype":"protein_coding","ncbi_id":"55893","summary":null,"start":28345585,"end":28402701,"strand":-1,"description":"zinc finger protein 395 [Source:HGNC Symbol;Acc:HGNC:18737]"}, {"versioned_ensembl_gene_id":"ENSG00000198793.12","gene_symbol":"MTOR","gene_name":"mechanistic target of rapamycin [Source:HGNC Symbol;Acc:HGNC:3942]","synonyms":"FRAP1,FRAP,FLJ44809,RAPT1,RAFT1,FRAP2","biotype":"protein_coding","ncbi_id":"2475","summary":"The protein encoded by this gene belongs to a family of phosphatidylinositol kinase-related kinases. These kinases mediate cellular responses to stresses such as DNA damage and nutrient deprivation. This kinase is a component of two distinct complexes, mTORC1, which controls protein synthesis, cell growth and proliferation, and mTORC2, which is a regulator of the actin cytoskeleton, and promotes cell survival and cell cycle progression. This protein acts as the target for the cell-cycle arrest and immunosuppressive effects of the FKBP12-rapamycin complex. Inhibitors of mTOR are used in organ transplants as immunosuppressants, and are being evaluated for their therapeutic potential in SARS-CoV-2 infections. Mutations in this gene are associated with Smith-Kingsmore syndrome and somatic focal cortical dysplasia type II. The ANGPTL7 gene is located in an intron of this gene. [provided by RefSeq, Aug 2020]","start":11106535,"end":11262507,"strand":-1,"description":"mechanistic target of rapamycin [Source:HGNC Symbol;Acc:HGNC:3942]"}, {"versioned_ensembl_gene_id":"ENSG00000253783.1","gene_symbol":"AC100807.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139114193,"end":139127953,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254258.1","gene_symbol":"AC087354.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":139460062,"end":139463016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275078.1","gene_symbol":"AC090093.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":139508701,"end":139508971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248767.2","gene_symbol":"AC187653.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":290170,"end":294422,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279943.1","gene_symbol":"FLJ38576","gene_name":"uncharacterized LOC651430 [Source:NCBI gene;Acc:651430]","synonyms":null,"biotype":"TEC","ncbi_id":"651430","summary":null,"start":186189032,"end":186191490,"strand":-1,"description":"uncharacterized LOC651430 [Source:NCBI gene;Acc:651430]"}, {"versioned_ensembl_gene_id":"ENSG00000275546.5","gene_symbol":"KIR2DL2","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]","synonyms":"nkat6,CD158k,cl-43,CD158B1","biotype":"protein_coding","ncbi_id":"3803","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54754663,"end":54769262,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6330]"}, {"versioned_ensembl_gene_id":"ENSG00000249574.1","gene_symbol":"AC226118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":379359,"end":382712,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228867.8","gene_symbol":"NRM","gene_name":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]","synonyms":"NRM29","biotype":"protein_coding","ncbi_id":"11270","summary":"The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":30732707,"end":30736080,"strand":-1,"description":"nurim (nuclear envelope membrane protein) [Source:HGNC Symbol;Acc:HGNC:8003]"}, {"versioned_ensembl_gene_id":"ENSG00000234471.1","gene_symbol":"AC147651.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":484107,"end":496118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117501.14","gene_symbol":"MROH9","gene_name":"maestro heat like repeat family member 9 [Source:HGNC Symbol;Acc:HGNC:26287]","synonyms":"C1orf129,FLJ23550,ARMC11","biotype":"protein_coding","ncbi_id":"80133","summary":null,"start":170935471,"end":171064765,"strand":1,"description":"maestro heat like repeat family member 9 [Source:HGNC Symbol;Acc:HGNC:26287]"}, {"versioned_ensembl_gene_id":"ENSG00000229159.1","gene_symbol":"TSPY23P","gene_name":"testis specific protein, Y-linked 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:38594]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100286964","summary":null,"start":22183850,"end":22186021,"strand":1,"description":"testis specific protein, Y-linked 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:38594]"}, {"versioned_ensembl_gene_id":"ENSG00000239446.1","gene_symbol":"AC004882.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29711820,"end":29719714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225615.1","gene_symbol":"RBMY2UP","gene_name":"RNA binding motif protein, Y-linked, family 2, member U pseudogene [Source:HGNC Symbol;Acc:HGNC:23898]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379009","summary":null,"start":22198429,"end":22203712,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member U pseudogene [Source:HGNC Symbol;Acc:HGNC:23898]"}, {"versioned_ensembl_gene_id":"ENSG00000232396.2","gene_symbol":"AC004882.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29705256,"end":29719859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218153.2","gene_symbol":"KRT18P22","gene_name":"keratin 18 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:33390]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442252","summary":null,"start":116457323,"end":116458669,"strand":-1,"description":"keratin 18 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:33390]"}, {"versioned_ensembl_gene_id":"ENSG00000249338.1","gene_symbol":"HMGB1P47","gene_name":"high mobility group box 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:39280]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873897","summary":null,"start":51409617,"end":51410205,"strand":-1,"description":"high mobility group box 1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:39280]"}, {"versioned_ensembl_gene_id":"ENSG00000275349.4","gene_symbol":"SMN1","gene_name":"survival of motor neuron 1, telomeric [Source:HGNC Symbol;Acc:HGNC:11117]","synonyms":"SMA2,SMA1,TDRD16A,SMA,SMNT,GEMIN1,SMA@,BCD541,SMA3","biotype":"protein_coding","ncbi_id":"6606","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. However, mutations in this gene, the telomeric copy, are associated with spinal muscular atrophy; mutations in the centromeric copy do not lead to disease. The centromeric copy may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Multiple transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2014]","start":70268827,"end":70296783,"strand":1,"description":"survival of motor neuron 1, telomeric [Source:HGNC Symbol;Acc:HGNC:11117]"}, {"versioned_ensembl_gene_id":"ENSG00000282486.1","gene_symbol":"LRRC37A9P","gene_name":"leucine rich repeat containing 37 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:43813]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533790","summary":null,"start":35912635,"end":35918010,"strand":-1,"description":"leucine rich repeat containing 37 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:43813]"}, {"versioned_ensembl_gene_id":"ENSG00000226342.1","gene_symbol":"NMD3P1","gene_name":"NMD3 ribosome export adaptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22672]","synonyms":"NMD3P","biotype":"processed_pseudogene","ncbi_id":"441238","summary":null,"start":63908966,"end":63910453,"strand":-1,"description":"NMD3 ribosome export adaptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:22672]"}, {"versioned_ensembl_gene_id":"ENSG00000226581.1","gene_symbol":"AC092634.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":63900823,"end":63917994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188820.12","gene_symbol":"FAM26F","gene_name":"family with sequence similarity 26 member F [Source:HGNC Symbol;Acc:HGNC:33391]","synonyms":"RP1-93H18.5,OTTHUMP00000017062,OTTHUMP00000017061,INAM,dJ93H18.5,C6orf187","biotype":"protein_coding","ncbi_id":"441168","summary":null,"start":116461370,"end":116463779,"strand":1,"description":"family with sequence similarity 26 member F [Source:HGNC Symbol;Acc:HGNC:33391]"}, {"versioned_ensembl_gene_id":"ENSG00000114204.14","gene_symbol":"SERPINI2","gene_name":"serpin family I member 2 [Source:HGNC Symbol;Acc:HGNC:8945]","synonyms":"MEPI,TSA2004,PI14,PANCPIN","biotype":"protein_coding","ncbi_id":"5276","summary":"The gene encodes a member of a family of proteins that acts as inhibitors of serine proteases. These proteins function in the regulation of a variety of physiological processes, including coagulation, fibrinolysis, development, malignancy, and inflammation. Expression of the encoded protein may be downregulated during pancreatic carcinogenesis. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013]","start":167441789,"end":167479004,"strand":-1,"description":"serpin family I member 2 [Source:HGNC Symbol;Acc:HGNC:8945]"}, {"versioned_ensembl_gene_id":"ENSG00000278494.2","gene_symbol":"RRN3","gene_name":"RRN3 homolog, RNA polymerase I transcription factor [Source:HGNC Symbol;Acc:HGNC:30346]","synonyms":"TIF-IA,DKFZp566E104","biotype":"protein_coding","ncbi_id":"54700","summary":null,"start":15002502,"end":15036801,"strand":1,"description":"RRN3 homolog, RNA polymerase I transcription factor [Source:HGNC Symbol;Acc:HGNC:30346]"}, {"versioned_ensembl_gene_id":"ENSG00000236569.3","gene_symbol":"HNRNPA1P73","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:48803]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129606","summary":null,"start":27328607,"end":27329534,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:48803]"}, {"versioned_ensembl_gene_id":"ENSG00000142619.4","gene_symbol":"PADI3","gene_name":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]","synonyms":"PDI3","biotype":"protein_coding","ncbi_id":"51702","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. The type III enzyme modulates hair structural proteins, such as filaggrin in the hair follicle and trichohyalin in the inner root sheath, during hair follicle formation. Together with the type I enzyme, this enzyme may also play a role in terminal differentiation of the epidermis. This gene exists in a cluster with four other paralogous genes. [provided by RefSeq, Jul 2008]","start":17249098,"end":17284233,"strand":1,"description":"peptidyl arginine deiminase 3 [Source:HGNC Symbol;Acc:HGNC:18337]"}, {"versioned_ensembl_gene_id":"ENSG00000185880.12","gene_symbol":"TRIM69","gene_name":"tripartite motif containing 69 [Source:HGNC Symbol;Acc:HGNC:17857]","synonyms":"TRIMLESS,Trif,RNF36","biotype":"protein_coding","ncbi_id":"140691","summary":"This gene encodes a member of the RING-B-box-coiled-coil (RBCC) family and encodes a protein with an N-terminal RING finger motif, a PRY domain and a C-terminal SPRY domain. The mouse ortholog of this gene is specifically expressed in germ cells at the round spermatid stages during spermatogenesis and, when overexpressed, induces apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":44728988,"end":44767829,"strand":1,"description":"tripartite motif containing 69 [Source:HGNC Symbol;Acc:HGNC:17857]"}, {"versioned_ensembl_gene_id":"ENSG00000112320.11","gene_symbol":"SOBP","gene_name":"sine oculis binding protein homolog [Source:HGNC Symbol;Acc:HGNC:29256]","synonyms":"FLJ10159","biotype":"protein_coding","ncbi_id":"55084","summary":"The protein encoded by this gene is a nuclear zinc finger protein that is involved in development of the cochlea. Defects in this gene have also been linked to intellectual disability. [provided by RefSeq, Mar 2011]","start":107489958,"end":107660167,"strand":1,"description":"sine oculis binding protein homolog [Source:HGNC Symbol;Acc:HGNC:29256]"}, {"versioned_ensembl_gene_id":"ENSG00000235927.4","gene_symbol":"NEXN-AS1","gene_name":"NEXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31983]","synonyms":"FLJ90637,C1orf118","biotype":"antisense_RNA","ncbi_id":"374987","summary":null,"start":77881348,"end":77889539,"strand":-1,"description":"NEXN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31983]"}, {"versioned_ensembl_gene_id":"ENSG00000244158.1","gene_symbol":"Z84488.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116460739,"end":116463692,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232830.5","gene_symbol":"AC110994.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":101414228,"end":101414633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248891.2","gene_symbol":"AC091860.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51427996,"end":51428427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139269.2","gene_symbol":"INHBE","gene_name":"inhibin beta E subunit [Source:HGNC Symbol;Acc:HGNC:24029]","synonyms":"MGC4638,activin","biotype":"protein_coding","ncbi_id":"83729","summary":"This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate an inhibin beta subunit. Inhibins have been implicated in regulating numerous cellular processes including cell proliferation, apoptosis, immune response and hormone secretion. This gene may be upregulated under conditions of endoplasmic reticulum stress, and this protein may inhibit cellular proliferation and growth in pancreas and liver. [provided by RefSeq, Sep 2016]","start":57452323,"end":57459280,"strand":1,"description":"inhibin beta E subunit [Source:HGNC Symbol;Acc:HGNC:24029]"}, {"versioned_ensembl_gene_id":"ENSG00000258294.5","gene_symbol":"AC090503.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":73115957,"end":73143858,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178252.17","gene_symbol":"WDR6","gene_name":"WD repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:12758]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11180","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. The encoded protein interacts with serine/threonine kinase 11, and is implicated in cell growth arrest. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]","start":49007062,"end":49015953,"strand":1,"description":"WD repeat domain 6 [Source:HGNC Symbol;Acc:HGNC:12758]"}, {"versioned_ensembl_gene_id":"ENSG00000231037.5","gene_symbol":"HCG25","gene_name":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]","synonyms":"dJ1033B10.16","biotype":"processed_transcript","ncbi_id":"414765","summary":null,"start":33403402,"end":33408857,"strand":1,"description":"HLA complex group 25 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:20196]"}, {"versioned_ensembl_gene_id":"ENSG00000234206.5","gene_symbol":"AL121957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107509803,"end":107511721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228801.5","gene_symbol":"AC064807.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51899325,"end":51947173,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133739.15","gene_symbol":"LRRCC1","gene_name":"leucine rich repeat and coiled-coil centrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:29373]","synonyms":"VFL1,KIAA1764,CLERC","biotype":"protein_coding","ncbi_id":"85444","summary":"This gene encodes a centrosomal protein that maintains the structural integrity of the centrosome and plays a key role in mitotic spindle formation. The encoded protein contains an N-terminal leucine-rich repeat domain and a C-terminal coiled-coil domain. It associates with the centrosome throughout the cell cycle and accumulates on the mitotic centrosome. [provided by RefSeq, Mar 2017]","start":85107147,"end":85146076,"strand":1,"description":"leucine rich repeat and coiled-coil centrosomal protein 1 [Source:HGNC Symbol;Acc:HGNC:29373]"}, {"versioned_ensembl_gene_id":"ENSG00000226552.2","gene_symbol":"BX284613.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171083565,"end":171085205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223618.7","gene_symbol":"VPS52","gene_name":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]","synonyms":"SACM2L,ARE1","biotype":"protein_coding","ncbi_id":"6293","summary":"This gene encodes a protein that is similar to the yeast suppressor of actin mutations 2 gene. The yeast protein forms a subunit of the tetrameric Golgi-associated retrograde protein complex that is involved in vesicle trafficking from from both early and late endosomes, back to the trans-Golgi network. This gene is located on chromosome 6 in a head-to-head orientation with the gene encoding ribosomal protein S18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":33404140,"end":33405839,"strand":-1,"description":"VPS52, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:10518]"}, {"versioned_ensembl_gene_id":"ENSG00000272024.1","gene_symbol":"AC064807.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51950284,"end":51950690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280135.1","gene_symbol":"AL096816.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":107697299,"end":107700218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253844.1","gene_symbol":"AC064807.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51961458,"end":52022974,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254136.1","gene_symbol":"AC064807.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51996210,"end":52008355,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235452.2","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"C6orf24,NG24,G6c","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31758101,"end":31761298,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000177938.4","gene_symbol":"CAPZA3","gene_name":"capping actin protein of muscle Z-line alpha subunit 3 [Source:HGNC Symbol;Acc:HGNC:24205]","synonyms":"Gsg3,CAPPA3","biotype":"protein_coding","ncbi_id":"93661","summary":"This gene encodes an actin capping protein, one of the F-actin capping protein alpha subunit family. The encoded protein is predominantly localized to the neck region of ejaculated sperm, other immunohistochemical signals were found in the tail and postacrosomal regions. The encoded protein may also form heterodimers of alpha and beta subunits. This protein may be important in determining sperm architecture and male fertility. [provided by RefSeq, Jul 2008]","start":18738101,"end":18739187,"strand":1,"description":"capping actin protein of muscle Z-line alpha subunit 3 [Source:HGNC Symbol;Acc:HGNC:24205]"}, {"versioned_ensembl_gene_id":"ENSG00000007933.12","gene_symbol":"FMO3","gene_name":"flavin containing monooxygenase 3 [Source:HGNC Symbol;Acc:HGNC:3771]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2328","summary":"Flavin-containing monooxygenases (FMO) are an important class of drug-metabolizing enzymes that catalyze the NADPH-dependent oxygenation of various nitrogen-,sulfur-, and phosphorous-containing xenobiotics such as therapeutic drugs, dietary compounds, pesticides, and other foreign compounds. The human FMO gene family is composed of 5 genes and multiple pseudogenes. FMO members have distinct developmental- and tissue-specific expression patterns. The expression of this FMO3 gene, the major FMO expressed in adult liver, can vary up to 20-fold between individuals. This inter-individual variation in FMO3 expression levels is likely to have significant effects on the rate at which xenobiotics are metabolised and, therefore, is of considerable interest to the pharmaceutical industry. This transmembrane protein localizes to the endoplasmic reticulum of many tissues. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Mutations in this gene cause the disorder trimethylaminuria (TMAu) which is characterized by the accumulation and excretion of unmetabolized trimethylamine and a distinctive body odor. In healthy individuals, trimethylamine is primarily converted to the non odorous trimethylamine N-oxide.[provided by RefSeq, Jan 2016]","start":171090877,"end":171117819,"strand":1,"description":"flavin containing monooxygenase 3 [Source:HGNC Symbol;Acc:HGNC:3771]"}, {"versioned_ensembl_gene_id":"ENSG00000227525.4","gene_symbol":"RPL7P6","gene_name":"ribosomal protein L7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32430]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"90193","summary":null,"start":19089151,"end":19089888,"strand":1,"description":"ribosomal protein L7 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32430]"}, {"versioned_ensembl_gene_id":"ENSG00000175707.8","gene_symbol":"KDF1","gene_name":"keratinocyte differentiation factor 1 [Source:HGNC Symbol;Acc:HGNC:26624]","synonyms":"RP11-344H11.3,FLJ34633,C1orf172","biotype":"protein_coding","ncbi_id":"126695","summary":null,"start":26949562,"end":26960406,"strand":-1,"description":"keratinocyte differentiation factor 1 [Source:HGNC Symbol;Acc:HGNC:26624]"}, {"versioned_ensembl_gene_id":"ENSG00000228090.6","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"C6orf25,G6b-B,G6b,NG31","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31758047,"end":31766164,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000166848.5","gene_symbol":"TERF2IP","gene_name":"TERF2 interacting protein [Source:HGNC Symbol;Acc:HGNC:19246]","synonyms":"RAP1","biotype":"protein_coding","ncbi_id":"54386","summary":"The gene encodes a protein that is part of a complex involved in telomere length regulation. Pseudogenes are present on chromosomes 5 and 22. [provided by RefSeq, Apr 2010]","start":75647786,"end":75761872,"strand":1,"description":"TERF2 interacting protein [Source:HGNC Symbol;Acc:HGNC:19246]"}, {"versioned_ensembl_gene_id":"ENSG00000197461.13","gene_symbol":"PDGFA","gene_name":"platelet derived growth factor subunit A [Source:HGNC Symbol;Acc:HGNC:8799]","synonyms":"PDGF1,PDGF-A","biotype":"protein_coding","ncbi_id":"5154","summary":"This gene encodes a member of the protein family comprised of both platelet-derived growth factors (PDGF) and vascular endothelial growth factors (VEGF). The encoded preproprotein is proteolytically processed to generate platelet-derived growth factor subunit A, which can homodimerize, or alternatively, heterodimerize with the related platelet-derived growth factor subunit B. These proteins bind and activate PDGF receptor tyrosine kinases, which play a role in a wide range of developmental processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]","start":497258,"end":520296,"strand":-1,"description":"platelet derived growth factor subunit A [Source:HGNC Symbol;Acc:HGNC:8799]"}, {"versioned_ensembl_gene_id":"ENSG00000283755.1","gene_symbol":"AC009122.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":75714224,"end":75726442,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284484.1","gene_symbol":"AC025287.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":75660227,"end":75677009,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261424.1","gene_symbol":"ATP5F1P7","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39748]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"124496","summary":null,"start":75709056,"end":75709815,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39748]"}, {"versioned_ensembl_gene_id":"ENSG00000256844.1","gene_symbol":"MEF2BNBP1","gene_name":"MEF2B neighbor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49883]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128109","summary":null,"start":19107854,"end":19108183,"strand":-1,"description":"MEF2B neighbor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49883]"}, {"versioned_ensembl_gene_id":"ENSG00000235586.1","gene_symbol":"AC011247.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38601598,"end":38602178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282757.3","gene_symbol":"DUXB","gene_name":"double homeobox B [Source:HGNC Symbol;Acc:HGNC:33345]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100033411","summary":null,"start":75693929,"end":75701459,"strand":-1,"description":"double homeobox B [Source:HGNC Symbol;Acc:HGNC:33345]"}, {"versioned_ensembl_gene_id":"ENSG00000125967.16","gene_symbol":"NECAB3","gene_name":"N-terminal EF-hand calcium binding protein 3 [Source:HGNC Symbol;Acc:HGNC:15851]","synonyms":"EFCBP3,dJ63M2.5,dJ63M2.4,APBA2BP,XB51,SYTIP2,NIP1","biotype":"protein_coding","ncbi_id":"63941","summary":"The protein encoded by this gene interacts with the amino-terminal domain of the neuron-specific X11-like protein (X11L), inhibits the association of X11L with amyloid precursor protein through a non-competitive mechanism, and abolishes the suppression of beta-amyloid production by X11L. This protein, together with X11L, may play an important role in the regulatory system of amyloid precursor protein metabolism and beta-amyloid generation. The protein is phosphorylated by NIMA-related expressed kinase 2, and localizes to the Golgi apparatus. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":33657087,"end":33674463,"strand":-1,"description":"N-terminal EF-hand calcium binding protein 3 [Source:HGNC Symbol;Acc:HGNC:15851]"}, {"versioned_ensembl_gene_id":"ENSG00000143889.15","gene_symbol":"HNRNPLL","gene_name":"heterogeneous nuclear ribonucleoprotein L like [Source:HGNC Symbol;Acc:HGNC:25127]","synonyms":"HNRPLL","biotype":"protein_coding","ncbi_id":"92906","summary":"HNRNPLL is a master regulator of activation-induced alternative splicing in T cells. In particular, it alters splicing of CD45 (PTPRC; MIM 151460), a tyrosine phosphatase essential for T-cell development and activation (Oberdoerffer et al., 2008 [PubMed 18669861]).[supplied by OMIM, Aug 2008]","start":38561978,"end":38603586,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein L like [Source:HGNC Symbol;Acc:HGNC:25127]"}, {"versioned_ensembl_gene_id":"ENSG00000172746.6","gene_symbol":"RPL12P13","gene_name":"ribosomal protein L12 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51936]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129926","summary":null,"start":26980165,"end":26980975,"strand":1,"description":"ribosomal protein L12 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:51936]"}, {"versioned_ensembl_gene_id":"ENSG00000065427.14","gene_symbol":"KARS","gene_name":"lysyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6215]","synonyms":"DFNB89,KARS2,KARS1","biotype":"protein_coding","ncbi_id":"3735","summary":"Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. Lysyl-tRNA synthetase is a homodimer localized to the cytoplasm which belongs to the class II family of tRNA synthetases. It has been shown to be a target of autoantibodies in the human autoimmune diseases, polymyositis or dermatomyositis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":75627474,"end":75648643,"strand":-1,"description":"lysyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6215]"}, {"versioned_ensembl_gene_id":"ENSG00000224064.1","gene_symbol":"AL356390.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26983628,"end":26984024,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225294.1","gene_symbol":"OSTCP2","gene_name":"oligosaccharyltransferase complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646567","summary":null,"start":26985897,"end":26986340,"strand":-1,"description":"oligosaccharyltransferase complex subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42864]"}, {"versioned_ensembl_gene_id":"ENSG00000165349.11","gene_symbol":"SLC7A3","gene_name":"solute carrier family 7 member 3 [Source:HGNC Symbol;Acc:HGNC:11061]","synonyms":"FLJ14541,CAT-3,ATRC3","biotype":"protein_coding","ncbi_id":"84889","summary":"This gene encodes a member of the solute carrier family 7. The encoded protein is a sodium-independent cationic amino acid transporter. Alternate splicing results in multiple transcripts that encoded the same protein.[provided by RefSeq, May 2010]","start":70925582,"end":70931125,"strand":-1,"description":"solute carrier family 7 member 3 [Source:HGNC Symbol;Acc:HGNC:11061]"}, {"versioned_ensembl_gene_id":"ENSG00000144152.12","gene_symbol":"FBLN7","gene_name":"fibulin 7 [Source:HGNC Symbol;Acc:HGNC:26740]","synonyms":"TM14,FLJ37440","biotype":"protein_coding","ncbi_id":"129804","summary":null,"start":112138385,"end":112188216,"strand":1,"description":"fibulin 7 [Source:HGNC Symbol;Acc:HGNC:26740]"}, {"versioned_ensembl_gene_id":"ENSG00000250980.1","gene_symbol":"AC113155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":152796063,"end":152796831,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120539.14","gene_symbol":"MASTL","gene_name":"microtubule associated serine/threonine kinase like [Source:HGNC Symbol;Acc:HGNC:19042]","synonyms":"THC2,Gwl,FLJ14813","biotype":"protein_coding","ncbi_id":"84930","summary":"This gene encodes a microtubule-associated serine/threonine kinase. Mutations at this locus have been associated with autosomal dominant thrombocytopenia, also known as thrombocytopenia-2. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Feb 2010]","start":27154824,"end":27186924,"strand":1,"description":"microtubule associated serine/threonine kinase like [Source:HGNC Symbol;Acc:HGNC:19042]"}, {"versioned_ensembl_gene_id":"ENSG00000164144.15","gene_symbol":"ARFIP1","gene_name":"ADP ribosylation factor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21496]","synonyms":"HSU52521","biotype":"protein_coding","ncbi_id":"27236","summary":null,"start":152779937,"end":152918463,"strand":1,"description":"ADP ribosylation factor interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:21496]"}, {"versioned_ensembl_gene_id":"ENSG00000103051.18","gene_symbol":"COG4","gene_name":"component of oligomeric golgi complex 4 [Source:HGNC Symbol;Acc:HGNC:18620]","synonyms":"DKFZP586E1519,COD1","biotype":"protein_coding","ncbi_id":"25839","summary":"The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]","start":70480568,"end":70523565,"strand":-1,"description":"component of oligomeric golgi complex 4 [Source:HGNC Symbol;Acc:HGNC:18620]"}, {"versioned_ensembl_gene_id":"ENSG00000279652.1","gene_symbol":"Z82217.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35992321,"end":36000469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212789.4","gene_symbol":"ST13P5","gene_name":"ST13, Hsp70 interacting protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:18556]","synonyms":"FAM10A5","biotype":"processed_pseudogene","ncbi_id":"144106","summary":null,"start":18261982,"end":18263091,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:18556]"}, {"versioned_ensembl_gene_id":"ENSG00000271691.1","gene_symbol":"AC140658.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33851785,"end":33852069,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225018.1","gene_symbol":"AC092647.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55876738,"end":55877024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260312.1","gene_symbol":"AC140658.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33857935,"end":33858864,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227499.1","gene_symbol":"AC092647.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55877912,"end":55878164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243795.1","gene_symbol":"LINC02044","gene_name":"long intergenic non-protein coding RNA 2044 [Source:HGNC Symbol;Acc:HGNC:52884]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929717","summary":null,"start":113142350,"end":113167819,"strand":-1,"description":"long intergenic non-protein coding RNA 2044 [Source:HGNC Symbol;Acc:HGNC:52884]"}, {"versioned_ensembl_gene_id":"ENSG00000204220.11","gene_symbol":"PFDN6","gene_name":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]","synonyms":"HKE2,H2-KE2,PFD6,KE-2","biotype":"protein_coding","ncbi_id":"10471","summary":"PFDN6 is a subunit of the heteromeric prefoldin complex that chaperones nascent actin (see MIM 102560) and alpha- and beta-tubulin (see MIM 602529 and MIM 191130, respectively) chains pending their transfer to the cytosolic chaperonin containing TCP1 (MIM 186980) (CCT) complex (Hansen et al., 1999 [PubMed 10209023]).[supplied by OMIM, Jul 2010]","start":33289302,"end":33298401,"strand":1,"description":"prefoldin subunit 6 [Source:HGNC Symbol;Acc:HGNC:4926]"}, {"versioned_ensembl_gene_id":"ENSG00000279289.1","gene_symbol":"AL136164.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":71386852,"end":71390829,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230597.1","gene_symbol":"AL136164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71328942,"end":71329806,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163608.14","gene_symbol":"NEPRO","gene_name":"nucleolus and neural progenitor protein [Source:HGNC Symbol;Acc:HGNC:24496]","synonyms":"NET17,DKFZP434F2021,C3orf17","biotype":"protein_coding","ncbi_id":"25871","summary":null,"start":113002440,"end":113019861,"strand":-1,"description":"nucleolus and neural progenitor protein [Source:HGNC Symbol;Acc:HGNC:24496]"}, {"versioned_ensembl_gene_id":"ENSG00000275962.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040829,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000276127.1","gene_symbol":"AL589935.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71251758,"end":71252988,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135220.10","gene_symbol":"UGT2A3","gene_name":"UDP glucuronosyltransferase family 2 member A3 [Source:HGNC Symbol;Acc:HGNC:28528]","synonyms":"FLJ21934","biotype":"protein_coding","ncbi_id":"79799","summary":null,"start":68928463,"end":68951791,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member A3 [Source:HGNC Symbol;Acc:HGNC:28528]"}, {"versioned_ensembl_gene_id":"ENSG00000279312.1","gene_symbol":"AL136164.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":71373253,"end":71375387,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232295.7","gene_symbol":"AL589935.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":71221457,"end":71328228,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146670.9","gene_symbol":"CDCA5","gene_name":"cell division cycle associated 5 [Source:HGNC Symbol;Acc:HGNC:14626]","synonyms":null,"biotype":"protein_coding","ncbi_id":"113130","summary":null,"start":65066300,"end":65084164,"strand":-1,"description":"cell division cycle associated 5 [Source:HGNC Symbol;Acc:HGNC:14626]"}, {"versioned_ensembl_gene_id":"ENSG00000233426.3","gene_symbol":"EIF3FP3","gene_name":"eukaryotic translation initiation factor 3 subunit F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37625]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"339799","summary":null,"start":58251440,"end":58252525,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit F pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37625]"}, {"versioned_ensembl_gene_id":"ENSG00000225226.1","gene_symbol":"LINC01795","gene_name":"long intergenic non-protein coding RNA 1795 [Source:HGNC Symbol;Acc:HGNC:52585]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374744","summary":null,"start":58275877,"end":58296548,"strand":1,"description":"long intergenic non-protein coding RNA 1795 [Source:HGNC Symbol;Acc:HGNC:52585]"}, {"versioned_ensembl_gene_id":"ENSG00000158246.7","gene_symbol":"FAM46B","gene_name":"family with sequence similarity 46 member B [Source:HGNC Symbol;Acc:HGNC:28273]","synonyms":"MGC16491","biotype":"protein_coding","ncbi_id":"115572","summary":null,"start":27005020,"end":27012836,"strand":-1,"description":"family with sequence 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Symbol;Acc:HGNC:33704]"}, {"versioned_ensembl_gene_id":"ENSG00000230629.2","gene_symbol":"RPS23P8","gene_name":"ribosomal protein S23 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35982]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653658","summary":null,"start":70962964,"end":70963293,"strand":1,"description":"ribosomal protein S23 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:35982]"}, {"versioned_ensembl_gene_id":"ENSG00000247157.6","gene_symbol":"LINC01252","gene_name":"long intergenic non-protein coding RNA 1252 [Source:HGNC Symbol;Acc:HGNC:27888]","synonyms":null,"biotype":"lincRNA","ncbi_id":"338817","summary":null,"start":11548030,"end":11590369,"strand":1,"description":"long intergenic non-protein coding RNA 1252 [Source:HGNC Symbol;Acc:HGNC:27888]"}, {"versioned_ensembl_gene_id":"ENSG00000188827.10","gene_symbol":"SLX4","gene_name":"SLX4 structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:23845]","synonyms":"KIAA1987,KIAA1784,FANCP,BTBD12","biotype":"protein_coding","ncbi_id":"84464","summary":"This gene encodes a protein that functions as an assembly component of multiple structure-specific endonucleases. These endonuclease complexes are required for repair of specific types of DNA lesions and critical for cellular responses to replication fork failure. Mutations in this gene were found in patients with Fanconi anemia. [provided by RefSeq, Sep 2016]","start":3581181,"end":3611598,"strand":-1,"description":"SLX4 structure-specific endonuclease subunit [Source:HGNC Symbol;Acc:HGNC:23845]"}, {"versioned_ensembl_gene_id":"ENSG00000264587.5","gene_symbol":"AC117569.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29518259,"end":29548241,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231043.3","gene_symbol":"AC007238.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58460292,"end":58462032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239789.5","gene_symbol":"MRPS17","gene_name":"mitochondrial ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:14047]","synonyms":"RPMS17,MRP-S17,HSPC011","biotype":"protein_coding","ncbi_id":"51373","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S17P family. The encoded protein is moderately conserved between human mitochondrial and prokaryotic ribosomal proteins. Pseudogenes corresponding to this gene are found on chromosomes 1p, 3p, 6q, 14p, 18q, and Xq. [provided by RefSeq, Jul 2008]","start":55951819,"end":55956501,"strand":1,"description":"mitochondrial ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:14047]"}, {"versioned_ensembl_gene_id":"ENSG00000227910.1","gene_symbol":"AC092634.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":63924787,"end":63926306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231430.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29824605,"end":29825584,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000225114.1","gene_symbol":"CR388220.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29932035,"end":29933027,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235764.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"SUP45L2,HCGVII","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30022006,"end":30023296,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000213645.2","gene_symbol":"SLC25A1P3","gene_name":"solute carrier family 25 member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43846]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644159","summary":null,"start":63931141,"end":63931968,"strand":1,"description":"solute carrier family 25 member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43846]"}, {"versioned_ensembl_gene_id":"ENSG00000233723.7","gene_symbol":"LINC01122","gene_name":"long intergenic non-protein coding RNA 1122 [Source:HGNC Symbol;Acc:HGNC:49267]","synonyms":"FLJ30838","biotype":"lincRNA","ncbi_id":"400955","summary":null,"start":58427799,"end":59063766,"strand":1,"description":"long intergenic non-protein coding RNA 1122 [Source:HGNC Symbol;Acc:HGNC:49267]"}, {"versioned_ensembl_gene_id":"ENSG00000233173.1","gene_symbol":"VN1R34P","gene_name":"vomeronasal 1 receptor 34 pseudogene [Source:HGNC Symbol;Acc:HGNC:37354]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100129587","summary":null,"start":63934449,"end":63935331,"strand":-1,"description":"vomeronasal 1 receptor 34 pseudogene [Source:HGNC Symbol;Acc:HGNC:37354]"}, {"versioned_ensembl_gene_id":"ENSG00000235536.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29849566,"end":29849694,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000232708.1","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29918020,"end":29920795,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000228874.1","gene_symbol":"AC090954.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15131848,"end":15132208,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277705.1","gene_symbol":"AC007450.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11507162,"end":11507408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231264.1","gene_symbol":"ARAFP1","gene_name":"ARAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50824]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421741","summary":null,"start":63937905,"end":63938509,"strand":-1,"description":"ARAF pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50824]"}, {"versioned_ensembl_gene_id":"ENSG00000249773.3","gene_symbol":"AC092647.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":55887277,"end":55955239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270863.1","gene_symbol":"DDX55P1","gene_name":"DEAD-box helicase 55 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49852]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129640","summary":null,"start":11512723,"end":11514136,"strand":1,"description":"DEAD-box helicase 55 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49852]"}, {"versioned_ensembl_gene_id":"ENSG00000235346.9","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29824187,"end":29828345,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000274551.1","gene_symbol":"AC007450.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":11516425,"end":11521686,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266296.1","gene_symbol":"AC027141.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28651732,"end":28653208,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265994.1","gene_symbol":"AC023932.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28785068,"end":28789260,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146729.9","gene_symbol":"NIPSNAP2","gene_name":"nipsnap homolog 2 [Source:HGNC Symbol;Acc:HGNC:4179]","synonyms":"GBAS","biotype":"protein_coding","ncbi_id":"2631","summary":"This gene encodes a member of the NipSnap family of proteins that may be involved in vesicular transport. The encoded protein is localized to mitochondria and plays a role in oxidative phosphorylation. A pseudogene of this gene is located on the long arm of chromosome 2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]","start":55951793,"end":56000181,"strand":1,"description":"nipsnap homolog 2 [Source:HGNC Symbol;Acc:HGNC:4179]"}, {"versioned_ensembl_gene_id":"ENSG00000176232.10","gene_symbol":"AC092634.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63980385,"end":63981477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213783.4","gene_symbol":"RPL35P4","gene_name":"ribosomal protein L35 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36285]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271006","summary":null,"start":27269357,"end":27269678,"strand":-1,"description":"ribosomal protein L35 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36285]"}, {"versioned_ensembl_gene_id":"ENSG00000230639.1","gene_symbol":"VN1R36P","gene_name":"vomeronasal 1 receptor 36 pseudogene [Source:HGNC Symbol;Acc:HGNC:37356]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312790","summary":null,"start":63965834,"end":63966124,"strand":-1,"description":"vomeronasal 1 receptor 36 pseudogene [Source:HGNC Symbol;Acc:HGNC:37356]"}, {"versioned_ensembl_gene_id":"ENSG00000228660.1","gene_symbol":"VN1R35P","gene_name":"vomeronasal 1 receptor 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:37355]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100312789","summary":null,"start":63963431,"end":63964123,"strand":-1,"description":"vomeronasal 1 receptor 35 pseudogene [Source:HGNC Symbol;Acc:HGNC:37355]"}, {"versioned_ensembl_gene_id":"ENSG00000271238.1","gene_symbol":"AC023932.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28824652,"end":28824826,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284534.1","gene_symbol":"AC092634.8","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":63959844,"end":63981477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227578.1","gene_symbol":"RPS3AP53","gene_name":"ribosomal protein S3a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:44500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287512","summary":null,"start":15141380,"end":15142157,"strand":1,"description":"ribosomal protein S3a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:44500]"}, {"versioned_ensembl_gene_id":"ENSG00000266479.1","gene_symbol":"AC105245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29256817,"end":29257060,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265980.1","gene_symbol":"AC074237.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":29278509,"end":29361963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256237.1","gene_symbol":"AC007450.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11541395,"end":11555838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279770.1","gene_symbol":"LINC00552","gene_name":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]","synonyms":null,"biotype":"TEC","ncbi_id":"100130386","summary":null,"start":113748511,"end":113751089,"strand":-1,"description":"long intergenic non-protein coding RNA 552 [Source:HGNC Symbol;Acc:HGNC:43692]"}, {"versioned_ensembl_gene_id":"ENSG00000261938.1","gene_symbol":"AC006111.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3581181,"end":3583266,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123989.13","gene_symbol":"CHPF","gene_name":"chondroitin polymerizing factor [Source:HGNC Symbol;Acc:HGNC:24291]","synonyms":"CSS2,CHSY2","biotype":"protein_coding","ncbi_id":"79586","summary":null,"start":219538947,"end":219543787,"strand":-1,"description":"chondroitin polymerizing factor [Source:HGNC Symbol;Acc:HGNC:24291]"}, {"versioned_ensembl_gene_id":"ENSG00000235863.3","gene_symbol":"B3GALT4","gene_name":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]","synonyms":"GalT4,beta3Gal-T4","biotype":"protein_coding","ncbi_id":"8705","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). This gene is oriented telomere to centromere in close proximity to the ribosomal protein S18 gene. The functionality of the encoded protein is limited to ganglioseries glycolipid biosynthesis. [provided by RefSeq, Jul 2008]","start":33277132,"end":33284832,"strand":1,"description":"beta-1,3-galactosyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:919]"}, {"versioned_ensembl_gene_id":"ENSG00000279655.1","gene_symbol":"AC004009.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":27380562,"end":27381206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281510.1","gene_symbol":"AC021146.15","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68855376,"end":68858370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169427.6","gene_symbol":"KCNK9","gene_name":"potassium two pore domain channel subfamily K member 9 [Source:HGNC Symbol;Acc:HGNC:6283]","synonyms":"TASK-3,K2p9.1,TASK3","biotype":"protein_coding","ncbi_id":"51305","summary":"This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH-dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel dysmorphism syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]","start":139600838,"end":139703056,"strand":-1,"description":"potassium two pore domain channel subfamily K member 9 [Source:HGNC Symbol;Acc:HGNC:6283]"}, {"versioned_ensembl_gene_id":"ENSG00000232254.1","gene_symbol":"CSF2RBP1","gene_name":"colony stimulating factor 2 receptor beta common subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2437]","synonyms":"CSF2RB2","biotype":"unprocessed_pseudogene","ncbi_id":"23772","summary":null,"start":36950529,"end":36953723,"strand":-1,"description":"colony stimulating factor 2 receptor beta common subunit pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2437]"}, {"versioned_ensembl_gene_id":"ENSG00000224322.1","gene_symbol":"AC004009.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27361843,"end":27409938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226882.9","gene_symbol":"GNL1","gene_name":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]","synonyms":"HSR1","biotype":"protein_coding","ncbi_id":"2794","summary":"The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq, Jul 2008]","start":30533598,"end":30549394,"strand":-1,"description":"G protein nucleolar 1 (putative) [Source:HGNC Symbol;Acc:HGNC:4413]"}, {"versioned_ensembl_gene_id":"ENSG00000272905.1","gene_symbol":"AC018648.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32845394,"end":32846061,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163463.11","gene_symbol":"KRTCAP2","gene_name":"keratinocyte associated protein 2 [Source:HGNC Symbol;Acc:HGNC:28942]","synonyms":"KCP2","biotype":"protein_coding","ncbi_id":"200185","summary":null,"start":155169408,"end":155173475,"strand":-1,"description":"keratinocyte associated protein 2 [Source:HGNC Symbol;Acc:HGNC:28942]"}, {"versioned_ensembl_gene_id":"ENSG00000266196.1","gene_symbol":"AC090506.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30713275,"end":30714286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280504.1","gene_symbol":"AC021146.13","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68867386,"end":68870910,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279734.1","gene_symbol":"AC090506.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30780006,"end":30780424,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227057.9","gene_symbol":"WDR46","gene_name":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]","synonyms":"BING4,UTP7,C6orf11","biotype":"protein_coding","ncbi_id":"9277","summary":null,"start":33279108,"end":33289527,"strand":-1,"description":"WD repeat domain 46 [Source:HGNC Symbol;Acc:HGNC:13923]"}, {"versioned_ensembl_gene_id":"ENSG00000092009.10","gene_symbol":"CMA1","gene_name":"chymase 1 [Source:HGNC Symbol;Acc:HGNC:2097]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1215","summary":"This gene encodes a chymotryptic serine proteinase that belongs to the peptidase family S1. It is expressed in mast cells and is thought to function in the degradation of the extracellular matrix, the regulation of submucosal gland secretion, and the generation of vasoactive peptides. In the heart and blood vessels, this protein, rather than angiotensin converting enzyme, is largely responsible for converting angiotensin I to the vasoactive peptide angiotensin II. Alternative splicing results in multiple variants. [provided by RefSeq, Apr 2015]","start":24505353,"end":24508265,"strand":-1,"description":"chymase 1 [Source:HGNC Symbol;Acc:HGNC:2097]"}, {"versioned_ensembl_gene_id":"ENSG00000280525.1","gene_symbol":"AC021146.14","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68879312,"end":68880086,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229234.1","gene_symbol":"RBMY1KP","gene_name":"RNA binding motif protein, Y-linked, family 1, member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:38750]","synonyms":"RBMY1K","biotype":"unprocessed_pseudogene","ncbi_id":"100874497","summary":null,"start":22209331,"end":22216580,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member K, pseudogene [Source:HGNC Symbol;Acc:HGNC:38750]"}, {"versioned_ensembl_gene_id":"ENSG00000230524.8","gene_symbol":"COL6A4P1","gene_name":"collagen type VI alpha 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33484]","synonyms":"VWA6,DVWA,DIVA,COL6A4P,COL6A4","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"344875","summary":"This transcribed pseudogene represents the 5' end of a presumed ortholog to a mouse gene which encodes a collagen VI alpha 4 chain protein (GeneID 68553). No complete ORF of comparable size to the mouse protein is found in this gene. The predicted protein lacks a signal peptide; however, this truncated collagen polypeptide may have achieved a different function as suggested by PubMed ID: 18622395. Evidence of in vivo translation is incomplete. A large chromosome break separates this pseudogene from the 3' end of the presumed ortholog (COL6A4P2, GeneID 646300) which is located downstream at chromosome 3q21.3. [provided by RefSeq, Jun 2009]","start":15151833,"end":15205959,"strand":-1,"description":"collagen type VI alpha 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33484]"}, {"versioned_ensembl_gene_id":"ENSG00000169972.11","gene_symbol":"PUSL1","gene_name":"pseudouridylate synthase-like 1 [Source:HGNC Symbol;Acc:HGNC:26914]","synonyms":"FLJ90811","biotype":"protein_coding","ncbi_id":"126789","summary":null,"start":1308567,"end":1311677,"strand":1,"description":"pseudouridylate synthase-like 1 [Source:HGNC Symbol;Acc:HGNC:26914]"}, {"versioned_ensembl_gene_id":"ENSG00000215560.2","gene_symbol":"TTTY5","gene_name":"testis-specific transcript, Y-linked 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16482]","synonyms":"TTY5,LINC00126","biotype":"lincRNA","ncbi_id":"83863","summary":"There is a single copy of this gene on chromosome Y at the center of the P3 palindrome. [provided by RefSeq, Jul 2008]","start":22296798,"end":22298876,"strand":-1,"description":"testis-specific transcript, Y-linked 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16482]"}, {"versioned_ensembl_gene_id":"ENSG00000259458.1","gene_symbol":"MGC15885","gene_name":"uncharacterized protein MGC15885 [Source:NCBI gene;Acc:197003]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"197003","summary":null,"start":62637172,"end":62645291,"strand":-1,"description":"uncharacterized protein MGC15885 [Source:NCBI gene;Acc:197003]"}, {"versioned_ensembl_gene_id":"ENSG00000229940.1","gene_symbol":"TSPY22P","gene_name":"testis specific protein, Y-linked 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38522]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100286996","summary":null,"start":22305925,"end":22307951,"strand":-1,"description":"testis specific protein, Y-linked 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:38522]"}, {"versioned_ensembl_gene_id":"ENSG00000170852.10","gene_symbol":"KBTBD2","gene_name":"kelch repeat and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21751]","synonyms":"DKFZP566C134,BKLHD1","biotype":"protein_coding","ncbi_id":"25948","summary":null,"start":32868172,"end":32894131,"strand":-1,"description":"kelch repeat and BTB domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21751]"}, {"versioned_ensembl_gene_id":"ENSG00000243040.6","gene_symbol":"RBMY2FP","gene_name":"RNA binding motif protein, Y-linked, family 2, member F pseudogene [Source:HGNC Symbol;Acc:HGNC:23891]","synonyms":"MGC26641","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"159162","summary":null,"start":22308859,"end":22321825,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member F pseudogene [Source:HGNC Symbol;Acc:HGNC:23891]"}, {"versioned_ensembl_gene_id":"ENSG00000254105.1","gene_symbol":"VENTXP6","gene_name":"VENT homeobox pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32216]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"552879","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":73651289,"end":73651602,"strand":1,"description":"VENT homeobox pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:32216]"}, {"versioned_ensembl_gene_id":"ENSG00000104343.19","gene_symbol":"UBE2W","gene_name":"ubiquitin conjugating enzyme E2 W [Source:HGNC Symbol;Acc:HGNC:25616]","synonyms":"UBC-16,FLJ11011","biotype":"protein_coding","ncbi_id":"55284","summary":"This gene encodes a nuclear-localized ubiquitin-conjugating enzyme (E2) that, along with ubiquitin-activating (E1) and ligating (E3) enzymes, coordinates the addition of a ubiquitin moiety to existing proteins. The encoded protein promotes the ubiquitination of Fanconi anemia complementation group proteins and may be important in the repair of DNA damage. There is a pseudogene for this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":73780097,"end":73878910,"strand":-1,"description":"ubiquitin conjugating enzyme E2 W [Source:HGNC Symbol;Acc:HGNC:25616]"}, {"versioned_ensembl_gene_id":"ENSG00000240534.1","gene_symbol":"RPL34P17","gene_name":"ribosomal protein L34 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36636]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271001","summary":null,"start":52313154,"end":52313500,"strand":-1,"description":"ribosomal protein L34 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36636]"}, {"versioned_ensembl_gene_id":"ENSG00000171914.16","gene_symbol":"TLN2","gene_name":"talin 2 [Source:HGNC Symbol;Acc:HGNC:15447]","synonyms":"KIAA0320,ILWEQ","biotype":"protein_coding","ncbi_id":"83660","summary":"This gene encodes a protein related to talin 1, a cytoskeletal protein that plays a significant role in the assembly of actin filaments and in spreading and migration of various cell types, including fibroblasts and osteoclasts. This protein has a different pattern of expression compared to talin 1 but, like talin 1, is thought to associate with unique transmembrane receptors to form novel linkages between extracellular matrices and the actin cytoskeleton. [provided by RefSeq, Jul 2008]","start":62390526,"end":62844631,"strand":1,"description":"talin 2 [Source:HGNC Symbol;Acc:HGNC:15447]"}, {"versioned_ensembl_gene_id":"ENSG00000254314.1","gene_symbol":"AC021915.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52150820,"end":52154892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259247.1","gene_symbol":"TTTY25P","gene_name":"testis-specific transcript, Y-linked 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:38524]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287026","summary":null,"start":22330452,"end":22332500,"strand":1,"description":"testis-specific transcript, Y-linked 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:38524]"}, {"versioned_ensembl_gene_id":"ENSG00000271625.1","gene_symbol":"PSMA6P4","gene_name":"proteasome subunit alpha 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39609]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"121906","summary":null,"start":97475742,"end":97476459,"strand":1,"description":"proteasome subunit alpha 6 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39609]"}, {"versioned_ensembl_gene_id":"ENSG00000226134.1","gene_symbol":"AL359502.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97675011,"end":97677963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237902.1","gene_symbol":"TSPY21P","gene_name":"testis specific protein, Y-linked 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:38101]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287055","summary":null,"start":22400403,"end":22402568,"strand":-1,"description":"testis specific protein, Y-linked 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:38101]"}, {"versioned_ensembl_gene_id":"ENSG00000269973.1","gene_symbol":"AC010969.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9936360,"end":9939590,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147488.11","gene_symbol":"ST18","gene_name":"ST18, C2H2C-type zinc finger [Source:HGNC Symbol;Acc:HGNC:18695]","synonyms":"ZC2HC10,ZC2H2C3,NZF3,KIAA0535,ZNF387","biotype":"protein_coding","ncbi_id":"9705","summary":null,"start":52110839,"end":52460959,"strand":-1,"description":"ST18, C2H2C-type zinc finger [Source:HGNC Symbol;Acc:HGNC:18695]"}, {"versioned_ensembl_gene_id":"ENSG00000261799.1","gene_symbol":"AC007406.5","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":273954,"end":277123,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140990.14","gene_symbol":"NDUFB10","gene_name":"NADH:ubiquinone oxidoreductase subunit B10 [Source:HGNC Symbol;Acc:HGNC:7696]","synonyms":"PDSW","biotype":"protein_coding","ncbi_id":"4716","summary":null,"start":1959508,"end":1961975,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit B10 [Source:HGNC Symbol;Acc:HGNC:7696]"}, {"versioned_ensembl_gene_id":"ENSG00000119900.7","gene_symbol":"OGFRL1","gene_name":"opioid growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:21378]","synonyms":"dJ331H24.1","biotype":"protein_coding","ncbi_id":"79627","summary":null,"start":71288803,"end":71308950,"strand":1,"description":"opioid growth factor receptor like 1 [Source:HGNC Symbol;Acc:HGNC:21378]"}, {"versioned_ensembl_gene_id":"ENSG00000273365.1","gene_symbol":"AL451074.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":165706556,"end":165707284,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279429.1","gene_symbol":"AC004009.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":27412164,"end":27412891,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258744.1","gene_symbol":"AL132800.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24501594,"end":24508688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088854.12","gene_symbol":"C20orf194","gene_name":"chromosome 20 open reading frame 194 [Source:HGNC Symbol;Acc:HGNC:17721]","synonyms":"DKFZp434N061","biotype":"protein_coding","ncbi_id":"25943","summary":"This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]","start":3249305,"end":3407625,"strand":-1,"description":"chromosome 20 open reading frame 194 [Source:HGNC Symbol;Acc:HGNC:17721]"}, {"versioned_ensembl_gene_id":"ENSG00000168566.12","gene_symbol":"SNRNP48","gene_name":"small nuclear ribonucleoprotein U11/U12 subunit 48 [Source:HGNC Symbol;Acc:HGNC:21368]","synonyms":"FLJ32234,dJ512B11.2,dJ336K20B.1,C6orf151","biotype":"protein_coding","ncbi_id":"154007","summary":null,"start":7590199,"end":7611967,"strand":1,"description":"small nuclear ribonucleoprotein U11/U12 subunit 48 [Source:HGNC Symbol;Acc:HGNC:21368]"}, {"versioned_ensembl_gene_id":"ENSG00000143149.12","gene_symbol":"ALDH9A1","gene_name":"aldehyde dehydrogenase 9 family member A1 [Source:HGNC Symbol;Acc:HGNC:412]","synonyms":"E3,ALDH9,ALDH7,ALDH4","biotype":"protein_coding","ncbi_id":"223","summary":"This protein belongs to the aldehyde dehydrogenase family of proteins. It has a high activity for oxidation of gamma-aminobutyraldehyde and other amino aldehydes. The enzyme catalyzes the dehydrogenation of gamma-aminobutyraldehyde to gamma-aminobutyric acid (GABA). This isozyme is a tetramer of identical 54-kD subunits. [provided by RefSeq, Jul 2008]","start":165662216,"end":165698863,"strand":-1,"description":"aldehyde dehydrogenase 9 family member A1 [Source:HGNC Symbol;Acc:HGNC:412]"}, {"versioned_ensembl_gene_id":"ENSG00000265670.1","gene_symbol":"AC016382.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30954820,"end":30980917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226723.2","gene_symbol":"AL513175.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":192246708,"end":192247487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271375.1","gene_symbol":"AC134879.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11473727,"end":11474237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162739.13","gene_symbol":"SLAMF6","gene_name":"SLAM family member 6 [Source:HGNC Symbol;Acc:HGNC:21392]","synonyms":"SF2000,NTBA,NTB-A,Ly108,KALIb,KALI,CD352","biotype":"protein_coding","ncbi_id":"114836","summary":"The protein encoded by this gene is a type I transmembrane protein, belonging to the CD2 subfamily of the immunoglobulin superfamily. This encoded protein is expressed on Natural killer (NK), T, and B lymphocytes. It undergoes tyrosine phosphorylation and associates with the Src homology 2 domain-containing protein (SH2D1A) as well as with SH2 domain-containing phosphatases (SHPs). It functions as a coreceptor in the process of NK cell activation. It can also mediate inhibitory signals in NK cells from X-linked lymphoproliferative patients. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]","start":160485030,"end":160523262,"strand":-1,"description":"SLAM family member 6 [Source:HGNC Symbol;Acc:HGNC:21392]"}, {"versioned_ensembl_gene_id":"ENSG00000233830.2","gene_symbol":"EIF4HP1","gene_name":"eukaryotic translation initiation factor 4H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49035]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401316","summary":null,"start":27458163,"end":27458849,"strand":-1,"description":"eukaryotic translation initiation factor 4H pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49035]"}, {"versioned_ensembl_gene_id":"ENSG00000281972.1","gene_symbol":"TRBVA","gene_name":"T-cell receptor beta variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12247]","synonyms":"TCRBV33S1","biotype":"TR_V_pseudogene","ncbi_id":"28556","summary":null,"start":142722076,"end":142722530,"strand":1,"description":"T-cell receptor beta variable A (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12247]"}, {"versioned_ensembl_gene_id":"ENSG00000213781.3","gene_symbol":"PSMC1P2","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39777]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442291","summary":null,"start":27461766,"end":27462969,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39777]"}, {"versioned_ensembl_gene_id":"ENSG00000223535.4","gene_symbol":"FAM90A17P","gene_name":"family with sequence similarity 90 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:32265]","synonyms":"FAM90A17","biotype":"unprocessed_pseudogene","ncbi_id":"728746","summary":null,"start":7746034,"end":7749606,"strand":1,"description":"family with sequence similarity 90 member A17, pseudogene [Source:HGNC Symbol;Acc:HGNC:32265]"}, {"versioned_ensembl_gene_id":"ENSG00000226941.8","gene_symbol":"RBMY1J","gene_name":"RNA binding motif protein, Y-linked, family 1, member J [Source:HGNC Symbol;Acc:HGNC:23917]","synonyms":null,"biotype":"protein_coding","ncbi_id":"378951","summary":"This gene encodes a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. This protein likely functions as a splicing factor during spermatogenesis. Multiple closely related paralogs of this gene are found in a gene cluster in the AZFb azoospermia factor region of chromosome Y. Most of these related copies are thought to be pseudogenes, though several likely encode functional proteins. [provided by RefSeq, Mar 2016]","start":22403461,"end":22417881,"strand":1,"description":"RNA binding motif protein, Y-linked, family 1, member J [Source:HGNC Symbol;Acc:HGNC:23917]"}, {"versioned_ensembl_gene_id":"ENSG00000135469.13","gene_symbol":"COQ10A","gene_name":"coenzyme Q10A [Source:HGNC Symbol;Acc:HGNC:26515]","synonyms":"FLJ32452","biotype":"protein_coding","ncbi_id":"93058","summary":null,"start":56266858,"end":56270966,"strand":1,"description":"coenzyme Q10A [Source:HGNC Symbol;Acc:HGNC:26515]"}, {"versioned_ensembl_gene_id":"ENSG00000234385.1","gene_symbol":"RCC2P1","gene_name":"regulator of chromosome condensation 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37710]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"650983","summary":null,"start":11781052,"end":11782527,"strand":-1,"description":"regulator of chromosome condensation 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37710]"}, {"versioned_ensembl_gene_id":"ENSG00000281308.1","gene_symbol":"UGT2B27P","gene_name":"UDP glucuronosyltransferase family 2 member B27, pseudogene [Source:HGNC Symbol;Acc:HGNC:12551]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"54569","summary":null,"start":68887233,"end":68892380,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B27, pseudogene [Source:HGNC Symbol;Acc:HGNC:12551]"}, {"versioned_ensembl_gene_id":"ENSG00000235574.1","gene_symbol":"AC073150.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27491682,"end":27492765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281968.1","gene_symbol":"TRBV26","gene_name":"T-cell receptor beta variable 26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12207]","synonyms":"TCRBV26S1,TCRBV28S1P","biotype":"TR_V_pseudogene","ncbi_id":"28561","summary":null,"start":142736369,"end":142736853,"strand":1,"description":"T-cell receptor beta variable 26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12207]"}, {"versioned_ensembl_gene_id":"ENSG00000236064.1","gene_symbol":"AL034399.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107894597,"end":107935980,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172673.10","gene_symbol":"THEMIS","gene_name":"thymocyte selection associated [Source:HGNC Symbol;Acc:HGNC:21569]","synonyms":"TSEPA,FLJ40584,C6orf207,C6orf190,bA325O24.4,bA325O24.3","biotype":"protein_coding","ncbi_id":"387357","summary":"This gene encodes a protein that plays a regulatory role in both positive and negative T-cell selection during late thymocyte development. The protein functions through T-cell antigen receptor signaling, and is necessary for proper lineage commitment and maturation of T-cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":127708072,"end":127918631,"strand":-1,"description":"thymocyte selection associated [Source:HGNC Symbol;Acc:HGNC:21569]"}, {"versioned_ensembl_gene_id":"ENSG00000280621.1","gene_symbol":"AC110772.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":186971648,"end":187014215,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000080561.13","gene_symbol":"MID2","gene_name":"midline 2 [Source:HGNC Symbol;Acc:HGNC:7096]","synonyms":"TRIM1,RNF60,MRX101,FXY2","biotype":"protein_coding","ncbi_id":"11043","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to microtubular structures in the cytoplasm. Alternate splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Feb 2009]","start":107825755,"end":107927193,"strand":1,"description":"midline 2 [Source:HGNC Symbol;Acc:HGNC:7096]"}, {"versioned_ensembl_gene_id":"ENSG00000178021.10","gene_symbol":"TSPYL6","gene_name":"TSPY like 6 [Source:HGNC Symbol;Acc:HGNC:14521]","synonyms":null,"biotype":"protein_coding","ncbi_id":"388951","summary":null,"start":54253184,"end":54256272,"strand":-1,"description":"TSPY like 6 [Source:HGNC Symbol;Acc:HGNC:14521]"}, {"versioned_ensembl_gene_id":"ENSG00000253100.1","gene_symbol":"AC009623.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25685798,"end":25687524,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241114.1","gene_symbol":"AC008280.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54079974,"end":54080280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134762.16","gene_symbol":"DSC3","gene_name":"desmocollin 3 [Source:HGNC Symbol;Acc:HGNC:3037]","synonyms":"DSC4,DSC2,DSC1,DSC,CDHF3","biotype":"protein_coding","ncbi_id":"1825","summary":"The protein encoded by this gene is a calcium-dependent glycoprotein that is a member of the desmocollin subfamily of the cadherin superfamily. These desmosomal family members, along with the desmogleins, are found primarily in epithelial cells where they constitute the adhesive proteins of the desmosome cell-cell junction and are required for cell adhesion and desmosome formation. The desmosomal family members are arranged in two clusters on chromosome 18, occupying less than 650 kb combined. Mutations in this gene are a cause of hypotrichosis and recurrent skin vesicles disorder. The protein can act as an autoantigen in pemphigus diseases, and it is also considered to be a biomarker for some cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014]","start":30990008,"end":31042815,"strand":-1,"description":"desmocollin 3 [Source:HGNC Symbol;Acc:HGNC:3037]"}, {"versioned_ensembl_gene_id":"ENSG00000233237.6","gene_symbol":"LINC00472","gene_name":"long intergenic non-protein coding RNA 472 [Source:HGNC Symbol;Acc:HGNC:21380]","synonyms":"FLJ13189,dJ288M22.3,C6orf155","biotype":"lincRNA","ncbi_id":"79940","summary":null,"start":71344344,"end":71420769,"strand":-1,"description":"long intergenic non-protein coding RNA 472 [Source:HGNC Symbol;Acc:HGNC:21380]"}, {"versioned_ensembl_gene_id":"ENSG00000170634.12","gene_symbol":"ACYP2","gene_name":"acylphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"98","summary":"Acylphosphatase can hydrolyze the phosphoenzyme intermediate of different membrane pumps, particularly the Ca2+/Mg2+-ATPase from sarcoplasmic reticulum of skeletal muscle. Two isoenzymes have been isolated, called muscle acylphosphatase and erythrocyte acylphosphatase on the basis of their tissue localization. This gene encodes the muscle-type isoform (MT). An increase of the MT isoform is associated with muscle differentiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]","start":53970838,"end":54305300,"strand":1,"description":"acylphosphatase 2 [Source:HGNC Symbol;Acc:HGNC:180]"}, {"versioned_ensembl_gene_id":"ENSG00000281916.1","gene_symbol":"AF250324.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189703881,"end":189704490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101608.12","gene_symbol":"MYL12A","gene_name":"myosin light chain 12A [Source:HGNC Symbol;Acc:HGNC:16701]","synonyms":"MYL2B,MRLC3,MRCL3,MLCB","biotype":"protein_coding","ncbi_id":"10627","summary":"This gene encodes a nonsarcomeric myosin regulatory light chain. This protein is activated by phosphorylation and regulates smooth muscle and non-muscle cell contraction. This protein may also be involved in DNA damage repair by sequestering the transcriptional regulator apoptosis-antagonizing transcription factor (AATF)/Che-1 which functions as a repressor of p53-driven apoptosis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 8.[provided by RefSeq, Dec 2014]","start":3247481,"end":3256236,"strand":1,"description":"myosin light chain 12A [Source:HGNC Symbol;Acc:HGNC:16701]"}, {"versioned_ensembl_gene_id":"ENSG00000278819.1","gene_symbol":"AC005156.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":92540268,"end":92557877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254548.1","gene_symbol":"AC105219.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143718246,"end":143718891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273088.1","gene_symbol":"AL713999.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":155169409,"end":155187272,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181085.14","gene_symbol":"MAPK15","gene_name":"mitogen-activated protein kinase 15 [Source:HGNC Symbol;Acc:HGNC:24667]","synonyms":"ERK8,ERK7","biotype":"protein_coding","ncbi_id":"225689","summary":null,"start":143716259,"end":143722458,"strand":1,"description":"mitogen-activated protein kinase 15 [Source:HGNC Symbol;Acc:HGNC:24667]"}, {"versioned_ensembl_gene_id":"ENSG00000164451.13","gene_symbol":"FAM26D","gene_name":"family with sequence similarity 26 member D [Source:HGNC Symbol;Acc:HGNC:21094]","synonyms":"C6orf78,FLJ32239","biotype":"protein_coding","ncbi_id":"221301","summary":null,"start":116529013,"end":116558868,"strand":1,"description":"family with sequence similarity 26 member D [Source:HGNC Symbol;Acc:HGNC:21094]"}, {"versioned_ensembl_gene_id":"ENSG00000268043.7","gene_symbol":"NBPF12","gene_name":"NBPF member 12 [Source:HGNC Symbol;Acc:HGNC:24297]","synonyms":"KIAA1245,COAS1","biotype":"protein_coding","ncbi_id":"149013","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013]","start":146938744,"end":146996202,"strand":1,"description":"NBPF member 12 [Source:HGNC Symbol;Acc:HGNC:24297]"}, {"versioned_ensembl_gene_id":"ENSG00000163462.17","gene_symbol":"TRIM46","gene_name":"tripartite motif containing 46 [Source:HGNC Symbol;Acc:HGNC:19019]","synonyms":"TRIFIC,FLJ23229","biotype":"protein_coding","ncbi_id":"80128","summary":null,"start":155173787,"end":155184971,"strand":1,"description":"tripartite motif containing 46 [Source:HGNC Symbol;Acc:HGNC:19019]"}, {"versioned_ensembl_gene_id":"ENSG00000274493.1","gene_symbol":"AL035470.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127909833,"end":127910052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236792.1","gene_symbol":"AL513175.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":192247505,"end":192247947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269966.1","gene_symbol":"AL136164.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71295173,"end":71417436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253148.1","gene_symbol":"RGS21","gene_name":"regulator of G protein signaling 21 [Source:HGNC Symbol;Acc:HGNC:26839]","synonyms":null,"biotype":"protein_coding","ncbi_id":"431704","summary":"Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. RGS proteins are GTPase-activating proteins for Gi (see GNAI1; MIM 139310) and Gq (see GNAQ; MIM 600998) class G-alpha proteins. They accelerate transit through the cycle of GTP binding and hydrolysis and thereby accelerate signaling kinetics and termination.[supplied by OMIM, Nov 2008]","start":192316992,"end":192367285,"strand":1,"description":"regulator of G protein signaling 21 [Source:HGNC Symbol;Acc:HGNC:26839]"}, {"versioned_ensembl_gene_id":"ENSG00000261191.1","gene_symbol":"AC013640.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36641186,"end":36669097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261315.2","gene_symbol":"AC103988.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":36617089,"end":36619265,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223518.5","gene_symbol":"CSNK1A1P1","gene_name":"casein kinase 1 alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30446]","synonyms":"CSNK1A1P","biotype":"transcribed_processed_pseudogene","ncbi_id":"161635","summary":null,"start":36798596,"end":36818459,"strand":-1,"description":"casein kinase 1 alpha 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30446]"}, {"versioned_ensembl_gene_id":"ENSG00000233291.1","gene_symbol":"RPL7AP61","gene_name":"ribosomal protein L7a pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:35482]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271539","summary":null,"start":97901653,"end":97902288,"strand":1,"description":"ribosomal protein L7a pseudogene 61 [Source:HGNC Symbol;Acc:HGNC:35482]"}, {"versioned_ensembl_gene_id":"ENSG00000225618.6","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1","biotype":"processed_transcript","ncbi_id":"80862","summary":null,"start":29990956,"end":30051969,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000270725.1","gene_symbol":"AL356580.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":97939356,"end":97953539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186073.11","gene_symbol":"C15orf41","gene_name":"chromosome 15 open reading frame 41 [Source:HGNC Symbol;Acc:HGNC:26929]","synonyms":"MGC11326,HH114,FLJ22851","biotype":"protein_coding","ncbi_id":"84529","summary":"This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]","start":36579611,"end":36810248,"strand":1,"description":"chromosome 15 open reading frame 41 [Source:HGNC Symbol;Acc:HGNC:26929]"}, {"versioned_ensembl_gene_id":"ENSG00000236069.1","gene_symbol":"AL136987.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":192529579,"end":192538102,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279673.1","gene_symbol":"AC092919.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":171460612,"end":171462256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232498.1","gene_symbol":"AL136987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":192517639,"end":192567217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136527.17","gene_symbol":"TRA2B","gene_name":"transformer 2 beta homolog [Source:HGNC Symbol;Acc:HGNC:10781]","synonyms":"SFRS10,PPP1R156,Htra2-beta","biotype":"protein_coding","ncbi_id":"6434","summary":"This gene encodes a nuclear protein which functions as sequence-specific serine/arginine splicing factor which plays a role in mRNA processing, splicing patterns, and gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":185915906,"end":185938136,"strand":-1,"description":"transformer 2 beta homolog [Source:HGNC Symbol;Acc:HGNC:10781]"}, {"versioned_ensembl_gene_id":"ENSG00000240497.2","gene_symbol":"AC092919.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":171468084,"end":171469633,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100448.3","gene_symbol":"CTSG","gene_name":"cathepsin G [Source:HGNC Symbol;Acc:HGNC:2532]","synonyms":"CG","biotype":"protein_coding","ncbi_id":"1511","summary":"The protein encoded by this gene, a member of the peptidase S1 protein family, is found in azurophil granules of neutrophilic polymorphonuclear leukocytes. The encoded protease has a specificity similar to that of chymotrypsin C, and may participate in the killing and digestion of engulfed pathogens, and in connective tissue remodeling at sites of inflammation. In addition, the encoded protein is antimicrobial, with bacteriocidal activity against S. aureus and N. gonorrhoeae. Transcript variants utilizing alternative polyadenylation signals exist for this gene. [provided by RefSeq, Sep 2014]","start":24573522,"end":24576260,"strand":-1,"description":"cathepsin G [Source:HGNC Symbol;Acc:HGNC:2532]"}, {"versioned_ensembl_gene_id":"ENSG00000234594.1","gene_symbol":"AC008134.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171534423,"end":171534615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218839.4","gene_symbol":"FAM138C","gene_name":"family with sequence similarity 138 member C [Source:HGNC Symbol;Acc:HGNC:32333]","synonyms":"F379","biotype":"lincRNA","ncbi_id":"654835","summary":null,"start":34394,"end":35871,"strand":-1,"description":"family with sequence similarity 138 member C [Source:HGNC Symbol;Acc:HGNC:32333]"}, {"versioned_ensembl_gene_id":"ENSG00000231841.1","gene_symbol":"FAM192BP","gene_name":"family with sequence similarity 192 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37194]","synonyms":"rcNIP30,FAM192B","biotype":"processed_pseudogene","ncbi_id":"152667","summary":null,"start":152927446,"end":152928207,"strand":1,"description":"family with sequence similarity 192 member B, pseudogene [Source:HGNC Symbol;Acc:HGNC:37194]"}, {"versioned_ensembl_gene_id":"ENSG00000068878.14","gene_symbol":"PSME4","gene_name":"proteasome activator subunit 4 [Source:HGNC Symbol;Acc:HGNC:20635]","synonyms":"PA200,KIAA0077","biotype":"protein_coding","ncbi_id":"23198","summary":null,"start":53864067,"end":53970840,"strand":-1,"description":"proteasome activator subunit 4 [Source:HGNC Symbol;Acc:HGNC:20635]"}, {"versioned_ensembl_gene_id":"ENSG00000215838.4","gene_symbol":"AL451074.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":165698750,"end":165709968,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139410.14","gene_symbol":"SDSL","gene_name":"serine dehydratase like [Source:HGNC Symbol;Acc:HGNC:30404]","synonyms":"SDS-RS1,cSDH","biotype":"protein_coding","ncbi_id":"113675","summary":null,"start":113422237,"end":113438276,"strand":1,"description":"serine dehydratase like [Source:HGNC Symbol;Acc:HGNC:30404]"}, {"versioned_ensembl_gene_id":"ENSG00000225272.2","gene_symbol":"AL451074.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165676310,"end":165676781,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230175.1","gene_symbol":"AL451074.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165671256,"end":165671725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178665.14","gene_symbol":"ZNF713","gene_name":"zinc finger protein 713 [Source:HGNC Symbol;Acc:HGNC:22043]","synonyms":"FLJ39963","biotype":"protein_coding","ncbi_id":"349075","summary":"The protein encoded by this gene contains C2H2 zinc finger domains. In some individuals, a CGG-repeat expansion from 5-22 repeats to 68-450 repeats has been identified in the first intron of this gene. This mutation is thought to effect the expression of this gene and it has been proposed that it may be associated with Autistic Spectrum Disorder. [provided by RefSeq, Jul 2016]","start":55887475,"end":55942225,"strand":1,"description":"zinc finger protein 713 [Source:HGNC Symbol;Acc:HGNC:22043]"}, {"versioned_ensembl_gene_id":"ENSG00000283601.1","gene_symbol":"AP003399.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":60577856,"end":60608418,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251125.1","gene_symbol":"AC091860.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51451158,"end":51462089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234507.9","gene_symbol":"BRD2","gene_name":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]","synonyms":"FSRG1,NAT,D6S113E,KIAA9001,RING3,BRD2-IT1","biotype":"protein_coding","ncbi_id":"6046","summary":"This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]","start":32890988,"end":32903839,"strand":1,"description":"bromodomain containing 2 [Source:HGNC Symbol;Acc:HGNC:1103]"}, {"versioned_ensembl_gene_id":"ENSG00000113384.13","gene_symbol":"GOLPH3","gene_name":"golgi phosphoprotein 3 [Source:HGNC Symbol;Acc:HGNC:15452]","synonyms":"GPP34,GOPP1,Vps74,MIDAS","biotype":"protein_coding","ncbi_id":"64083","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a peripheral membrane protein of the Golgi stack and may have a regulatory role in Golgi trafficking. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of these variants has not been determined. [provided by RefSeq, Jul 2008]","start":32124704,"end":32174350,"strand":-1,"description":"golgi phosphoprotein 3 [Source:HGNC Symbol;Acc:HGNC:15452]"}, {"versioned_ensembl_gene_id":"ENSG00000230860.1","gene_symbol":"CCNB1IP1P2","gene_name":"cyclin B1 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37694]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100505892","summary":null,"start":45567990,"end":45568807,"strand":-1,"description":"cyclin B1 interacting protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:37694]"}, {"versioned_ensembl_gene_id":"ENSG00000106049.8","gene_symbol":"HIBADH","gene_name":"3-hydroxyisobutyrate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4907]","synonyms":"NS5ATP1","biotype":"protein_coding","ncbi_id":"11112","summary":"This gene encodes a mitochondrial 3-hydroxyisobutyrate dehydrogenase enzyme. The encoded protein plays a critical role in the catabolism of L-valine by catalyzing the oxidation of 3-hydroxyisobutyrate to methylmalonate semialdehyde. [provided by RefSeq, Nov 2011]","start":27525442,"end":27662995,"strand":-1,"description":"3-hydroxyisobutyrate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:4907]"}, {"versioned_ensembl_gene_id":"ENSG00000100314.3","gene_symbol":"CABP7","gene_name":"calcium binding protein 7 [Source:HGNC Symbol;Acc:HGNC:20834]","synonyms":"MGC57793","biotype":"protein_coding","ncbi_id":"164633","summary":null,"start":29720084,"end":29731839,"strand":1,"description":"calcium binding protein 7 [Source:HGNC Symbol;Acc:HGNC:20834]"}, {"versioned_ensembl_gene_id":"ENSG00000158901.11","gene_symbol":"WFDC8","gene_name":"WAP four-disulfide core domain 8 [Source:HGNC Symbol;Acc:HGNC:16163]","synonyms":"WAP8,dJ461P17.1,C20orf170","biotype":"protein_coding","ncbi_id":"90199","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. The encoded protein contains a Kunitz-inhibitor domain, in addition to three WFDC domains. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Two alternatively spliced transcript variants have been found for this gene, and they encode the same protein. [provided by RefSeq, Jul 2008]","start":45551153,"end":45579326,"strand":-1,"description":"WAP four-disulfide core domain 8 [Source:HGNC Symbol;Acc:HGNC:16163]"}, {"versioned_ensembl_gene_id":"ENSG00000185485.14","gene_symbol":"SDHAP1","gene_name":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32455]","synonyms":"SDHALP1,SDHAL1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"255812","summary":null,"start":195959748,"end":195990318,"strand":-1,"description":"succinate dehydrogenase complex flavoprotein subunit A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32455]"}, {"versioned_ensembl_gene_id":"ENSG00000249270.1","gene_symbol":"KATNBL1P4","gene_name":"katanin regulatory subunit B1 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49054]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128982","summary":null,"start":51930808,"end":51932036,"strand":1,"description":"katanin regulatory subunit B1 like 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49054]"}, {"versioned_ensembl_gene_id":"ENSG00000187118.12","gene_symbol":"CMC1","gene_name":"C-X9-C motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28783]","synonyms":"MGC61571,C3orf68","biotype":"protein_coding","ncbi_id":"152100","summary":null,"start":28241584,"end":28325142,"strand":1,"description":"C-X9-C motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28783]"}, {"versioned_ensembl_gene_id":"ENSG00000171819.4","gene_symbol":"ANGPTL7","gene_name":"angiopoietin like 7 [Source:HGNC Symbol;Acc:HGNC:24078]","synonyms":"CDT6,AngX","biotype":"protein_coding","ncbi_id":"10218","summary":null,"start":11189341,"end":11195981,"strand":1,"description":"angiopoietin like 7 [Source:HGNC Symbol;Acc:HGNC:24078]"}, {"versioned_ensembl_gene_id":"ENSG00000100319.12","gene_symbol":"ZMAT5","gene_name":"zinc finger matrin-type 5 [Source:HGNC Symbol;Acc:HGNC:28046]","synonyms":"ZC3H19,SNRNP20","biotype":"protein_coding","ncbi_id":"55954","summary":null,"start":29730956,"end":29767011,"strand":-1,"description":"zinc finger matrin-type 5 [Source:HGNC Symbol;Acc:HGNC:28046]"}, {"versioned_ensembl_gene_id":"ENSG00000258657.5","gene_symbol":"AL136018.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":24595723,"end":24657774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254352.1","gene_symbol":"AC100854.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78723796,"end":78724136,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178033.5","gene_symbol":"FAM26E","gene_name":"family with sequence similarity 26 member E [Source:HGNC Symbol;Acc:HGNC:21568]","synonyms":"C6orf188,MGC45451,dJ493F7.3","biotype":"protein_coding","ncbi_id":"254228","summary":null,"start":116511646,"end":116524792,"strand":1,"description":"family with sequence similarity 26 member E [Source:HGNC Symbol;Acc:HGNC:21568]"}, {"versioned_ensembl_gene_id":"ENSG00000104427.11","gene_symbol":"ZC2HC1A","gene_name":"zinc finger C2HC-type containing 1A [Source:HGNC Symbol;Acc:HGNC:24277]","synonyms":"FAM164A,CGI-62,C8orf70","biotype":"protein_coding","ncbi_id":"51101","summary":null,"start":78666047,"end":78719765,"strand":1,"description":"zinc finger C2HC-type containing 1A [Source:HGNC Symbol;Acc:HGNC:24277]"}, {"versioned_ensembl_gene_id":"ENSG00000100453.12","gene_symbol":"GZMB","gene_name":"granzyme B [Source:HGNC Symbol;Acc:HGNC:4709]","synonyms":"CTLA1,CSPB,CSP-B,CGL1,CGL-1,CCPI,SECT,HLP,CTSGL1","biotype":"protein_coding","ncbi_id":"3002","summary":"This gene encodes a member of the granzyme subfamily of proteins, part of the peptidase S1 family of serine proteases. The encoded preproprotein is secreted by natural killer (NK) cells and cytotoxic T lymphocytes (CTLs) and proteolytically processed to generate the active protease, which induces target cell apoptosis. This protein also processes cytokines and degrades extracellular matrix proteins, and these roles are implicated in chronic inflammation and wound healing. Expression of this gene may be elevated in human patients with cardiac fibrosis. [provided by RefSeq, Sep 2016]","start":24630954,"end":24634267,"strand":-1,"description":"granzyme B [Source:HGNC Symbol;Acc:HGNC:4709]"}, {"versioned_ensembl_gene_id":"ENSG00000181995.11","gene_symbol":"LINC00301","gene_name":"long intergenic non-protein coding RNA 301 [Source:HGNC Symbol;Acc:HGNC:28603]","synonyms":"NCRNA00301,MGC39681,C11orf64","biotype":"lincRNA","ncbi_id":"283197","summary":null,"start":60615736,"end":60687149,"strand":1,"description":"long intergenic non-protein coding RNA 301 [Source:HGNC Symbol;Acc:HGNC:28603]"}, {"versioned_ensembl_gene_id":"ENSG00000184731.5","gene_symbol":"FAM110C","gene_name":"family with sequence similarity 110 member C [Source:HGNC Symbol;Acc:HGNC:33340]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642273","summary":null,"start":38814,"end":46870,"strand":-1,"description":"family with sequence similarity 110 member C [Source:HGNC Symbol;Acc:HGNC:33340]"}, {"versioned_ensembl_gene_id":"ENSG00000258260.1","gene_symbol":"AC073896.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":56267793,"end":56270104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238168.5","gene_symbol":"AC137055.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111581379,"end":111581773,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234117.2","gene_symbol":"AL445224.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":116492297,"end":116497099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283445.1","gene_symbol":"AL136985.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58715609,"end":58771295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258099.1","gene_symbol":"ATXN2-AS","gene_name":"ATXN2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51838]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723619","summary":null,"start":111599498,"end":111600256,"strand":1,"description":"ATXN2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51838]"}, {"versioned_ensembl_gene_id":"ENSG00000237812.2","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"HCGIX,HCGIX4,HCGIX-4,PERB11","biotype":"processed_transcript","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29964383,"end":29967676,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000156983.15","gene_symbol":"BRPF1","gene_name":"bromodomain and PHD finger containing 1 [Source:HGNC Symbol;Acc:HGNC:14255]","synonyms":"BR140","biotype":"protein_coding","ncbi_id":"7862","summary":"This gene encodes a bromodomain, PHD finger and chromo/Tudor-related Pro-Trp-Trp-Pro (PWWP) domain containing protein. The encoded protein is a component of the MOZ/MORF histone acetyltransferase complexes which function as a transcriptional regulators. This protein binds to the catalytic MYST domains of the MOZ and MORF proteins and may play a role in stimulating acetyltransferase and transcriptional activity of the complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":9731729,"end":9748018,"strand":1,"description":"bromodomain and PHD finger containing 1 [Source:HGNC Symbol;Acc:HGNC:14255]"}, {"versioned_ensembl_gene_id":"ENSG00000173626.9","gene_symbol":"TRAPPC3L","gene_name":"trafficking protein particle complex 3 like [Source:HGNC Symbol;Acc:HGNC:21090]","synonyms":"FLJ11180,BET3L,bA259P20.2","biotype":"protein_coding","ncbi_id":"100128327","summary":null,"start":116494989,"end":116545610,"strand":-1,"description":"trafficking protein particle complex 3 like [Source:HGNC Symbol;Acc:HGNC:21090]"}, {"versioned_ensembl_gene_id":"ENSG00000251168.1","gene_symbol":"AC025174.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7924292,"end":7925398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168468.12","gene_symbol":"ATF6B","gene_name":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]","synonyms":"CREBL1,G13","biotype":"protein_coding","ncbi_id":"1388","summary":"The protein encoded by this gene is a transcription factor in the unfolded protein response (UPR) pathway during ER stress. Either as a homodimer or as a heterodimer with ATF6-alpha, the encoded protein binds to the ER stress response element, interacting with nuclear transcription factor Y to activate UPR target genes. The protein is normally found in the membrane of the endoplasmic reticulum; however, under ER stress, the N-terminal cytoplasmic domain is cleaved from the rest of the protein and translocates to the nucleus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]","start":32091037,"end":32104024,"strand":-1,"description":"activating transcription factor 6 beta [Source:HGNC Symbol;Acc:HGNC:2349]"}, {"versioned_ensembl_gene_id":"ENSG00000273399.2","gene_symbol":"AL159169.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14586766,"end":14587326,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280338.1","gene_symbol":"AC091941.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8080186,"end":8080761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272871.1","gene_symbol":"AL159169.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14588797,"end":14590065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227061.1","gene_symbol":"AC079779.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197569,"end":202605,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279852.1","gene_symbol":"AC083964.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":486117,"end":488512,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204842.14","gene_symbol":"ATXN2","gene_name":"ataxin 2 [Source:HGNC Symbol;Acc:HGNC:10555]","synonyms":"TNRC13,SCA2,ATX2","biotype":"protein_coding","ncbi_id":"6311","summary":"This gene belongs to a group of genes that is associated with microsatellite-expansion diseases, a class of neurological and neuromuscular disorders caused by expansion of short stretches of repetitive DNA. The protein encoded by this gene has two globular domains near the N-terminus, one of which contains a clathrin-mediated trans-Golgi signal and an endoplasmic reticulum exit signal. The encoded cytoplasmic protein localizes to the endoplasmic reticulum and plasma membrane, is involved in endocytosis, and modulates mTOR signals, modifying ribosomal translation and mitochondrial function. The N-terminal region of the protein contains a polyglutamine tract of 14-31 residues that can be expanded in the pathogenic state to 32-200 residues. Intermediate length expansions of this tract increase susceptibility to amyotrophic lateral sclerosis, while long expansions of this tract result in spinocerebellar ataxia-2, an autosomal-dominantly inherited, neurodegenerative disorder. Genome-wide association studies indicate that loss-of-function mutations in this gene may be associated with susceptibility to type I diabetes, obesity and hypertension. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":111452214,"end":111599676,"strand":-1,"description":"ataxin 2 [Source:HGNC Symbol;Acc:HGNC:10555]"}, {"versioned_ensembl_gene_id":"ENSG00000223855.1","gene_symbol":"HRAT92","gene_name":"heart tissue-associated transcript 92 [Source:NCBI gene;Acc:441307]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441307","summary":null,"start":520391,"end":525232,"strand":1,"description":"heart tissue-associated transcript 92 [Source:NCBI gene;Acc:441307]"}, {"versioned_ensembl_gene_id":"ENSG00000264235.5","gene_symbol":"AP005329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3255436,"end":3261850,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188373.4","gene_symbol":"C10orf99","gene_name":"chromosome 10 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:31428]","synonyms":"UNQ1833,RLLV1833,FLJ21763,CSBF,AP-57","biotype":"protein_coding","ncbi_id":"387695","summary":null,"start":84173738,"end":84185294,"strand":1,"description":"chromosome 10 open reading frame 99 [Source:HGNC Symbol;Acc:HGNC:31428]"}, {"versioned_ensembl_gene_id":"ENSG00000101290.13","gene_symbol":"CDS2","gene_name":"CDP-diacylglycerol synthase 2 [Source:HGNC Symbol;Acc:HGNC:1801]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8760","summary":"Breakdown products of phosphoinositides are ubiquitous second messengers that function downstream of many G protein-coupled receptors and tyrosine kinases regulating cell growth, calcium metabolism, and protein kinase C activity. This gene encodes an enzyme which regulates the amount of phosphatidylinositol available for signaling by catalyzing the conversion of phosphatidic acid to CDP-diacylglycerol. This enzyme is an integral membrane protein localized to two subcellular domains, the matrix side of the inner mitochondrial membrane where it is thought to be involved in the synthesis of phosphatidylglycerol and cardiolipin and the cytoplasmic side of the endoplasmic reticulum where it functions in phosphatidylinositol biosynthesis. Two genes encoding this enzyme have been identified in humans, one mapping to human chromosome 4q21 and a second to 20p13. [provided by RefSeq, Jul 2008]","start":5126786,"end":5197887,"strand":1,"description":"CDP-diacylglycerol synthase 2 [Source:HGNC Symbol;Acc:HGNC:1801]"}, {"versioned_ensembl_gene_id":"ENSG00000231941.1","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3,bQB90C11.3,HCG4P6","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29917544,"end":29918534,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000180190.11","gene_symbol":"TDRP","gene_name":"testis development related protein [Source:HGNC Symbol;Acc:HGNC:26951]","synonyms":"TDRP2,TDRP1,INM01,C8orf42","biotype":"protein_coding","ncbi_id":"157695","summary":null,"start":489792,"end":545781,"strand":-1,"description":"testis development related protein [Source:HGNC Symbol;Acc:HGNC:26951]"}, {"versioned_ensembl_gene_id":"ENSG00000231719.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29984382,"end":29985259,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000066294.14","gene_symbol":"CD84","gene_name":"CD84 molecule [Source:HGNC Symbol;Acc:HGNC:1704]","synonyms":"SLAMF5,mCD84,hCD84","biotype":"protein_coding","ncbi_id":"8832","summary":"This gene encodes a membrane glycoprotein that is a member of the signaling lymphocyte activation molecule (SLAM) family. This family forms a subset of the larger CD2 cell-surface receptor Ig superfamily. The encoded protein is a homophilic adhesion molecule that is expressed in numerous immune cells types and is involved in regulating receptor-mediated signaling in those cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":160541095,"end":160579516,"strand":-1,"description":"CD84 molecule [Source:HGNC Symbol;Acc:HGNC:1704]"}, {"versioned_ensembl_gene_id":"ENSG00000118680.12","gene_symbol":"MYL12B","gene_name":"myosin light chain 12B [Source:HGNC Symbol;Acc:HGNC:29827]","synonyms":"MRLC2","biotype":"protein_coding","ncbi_id":"103910","summary":"The activity of nonmuscle myosin II (see MYH9; MIM 160775) is regulated by phosphorylation of a regulatory light chain, such as MRLC2. This phosphorylation results in higher MgATPase activity and the assembly of myosin II filaments (Iwasaki et al., 2001 [PubMed 11942626]).[supplied by OMIM, Mar 2008]","start":3261909,"end":3278284,"strand":1,"description":"myosin light chain 12B [Source:HGNC Symbol;Acc:HGNC:29827]"}, {"versioned_ensembl_gene_id":"ENSG00000154438.7","gene_symbol":"ASZ1","gene_name":"ankyrin repeat, SAM and basic leucine zipper domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1350]","synonyms":"Orf3,GASZ,CT1.19,C7orf7,ANKL1,ALP1","biotype":"protein_coding","ncbi_id":"136991","summary":null,"start":117363222,"end":117428123,"strand":-1,"description":"ankyrin repeat, SAM and basic leucine zipper domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1350]"}, {"versioned_ensembl_gene_id":"ENSG00000011007.12","gene_symbol":"ELOA","gene_name":"elongin A [Source:HGNC Symbol;Acc:HGNC:11620]","synonyms":"TCEB3A,TCEB3,SIII","biotype":"protein_coding","ncbi_id":"6924","summary":"This gene encodes the protein elongin A, which is a subunit of the transcription factor B (SIII) complex. The SIII complex is composed of elongins A/A2, B and C. It activates elongation by RNA polymerase II by suppressing transient pausing of the polymerase at many sites within transcription units. Elongin A functions as the transcriptionally active component of the SIII complex, whereas elongins B and C are regulatory subunits. Elongin A2 is specifically expressed in the testis, and capable of forming a stable complex with elongins B and C. The von Hippel-Lindau tumor suppressor protein binds to elongins B and C, and thereby inhibits transcription elongation. [provided by RefSeq, Jul 2008]","start":23743155,"end":23762059,"strand":1,"description":"elongin A [Source:HGNC Symbol;Acc:HGNC:11620]"}, {"versioned_ensembl_gene_id":"ENSG00000206398.5","gene_symbol":"LY6G6C","gene_name":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]","synonyms":"C6orf24,NG24,G6c","biotype":"protein_coding","ncbi_id":"80740","summary":"LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31708869,"end":31712066,"strand":-1,"description":"lymphocyte antigen 6 family member G6C [Source:HGNC Symbol;Acc:HGNC:13936]"}, {"versioned_ensembl_gene_id":"ENSG00000089597.16","gene_symbol":"GANAB","gene_name":"glucosidase II alpha subunit [Source:HGNC Symbol;Acc:HGNC:4138]","synonyms":"KIAA0088,GluII,GIIA,G2AN","biotype":"protein_coding","ncbi_id":"23193","summary":"This gene encodes the alpha subunit of glucosidase II and a member of the glycosyl hydrolase 31 family of proteins. The heterodimeric enzyme glucosidase II plays a role in protein folding and quality control by cleaving glucose residues from immature glycoproteins in the endoplasmic reticulum. Expression of the encoded protein is elevated in lung tumor tissue and in response to UV irradiation. Mutations in this gene cause autosomal-dominant polycystic kidney and liver disease. [provided by RefSeq, Jul 2016]","start":62624826,"end":62646726,"strand":-1,"description":"glucosidase II alpha subunit [Source:HGNC Symbol;Acc:HGNC:4138]"}, {"versioned_ensembl_gene_id":"ENSG00000231067.1","gene_symbol":"BX005091.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29931354,"end":29932345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253919.1","gene_symbol":"THAP12P7","gene_name":"THAP domain containing 12 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39574]","synonyms":"PRKRIRP7","biotype":"processed_pseudogene","ncbi_id":"100422712","summary":null,"start":78760142,"end":78762431,"strand":-1,"description":"THAP domain containing 12 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39574]"}, {"versioned_ensembl_gene_id":"ENSG00000231385.1","gene_symbol":"BX005091.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29995393,"end":29996388,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104432.13","gene_symbol":"IL7","gene_name":"interleukin 7 [Source:HGNC Symbol;Acc:HGNC:6023]","synonyms":"IL-7","biotype":"protein_coding","ncbi_id":"3574","summary":"The protein encoded by this gene is a cytokine important for B and T cell development. This cytokine and the hepatocyte growth factor (HGF) form a heterodimer that functions as a pre-pro-B cell growth-stimulating factor. IL7 is found to be a cofactor for V(D)J rearrangement of the T cell receptor beta (TCRB) during early T cell development. This cytokine can be produced locally by intestinal epithelial and epithelial goblet cells, and may serve as a regulatory factor for intestinal mucosal lymphocytes. IL7 plays an essential role in lymphoid cell survival, and in the maintenance of naive and memory T cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their presence in normal tissues has not been confirmed. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can be a potent inducer of proinflammatory cytokines and chemokines which may defend against the infection, but may also mediate destructive lung injury. Elevated serum IL7 levels, together with several other circulating cytokines and chemokines, has been found to be associated with the severity of Coronavirus Disease 19 (COVID-19). [provided by RefSeq, Jul 2020]","start":78675743,"end":78805523,"strand":-1,"description":"interleukin 7 [Source:HGNC Symbol;Acc:HGNC:6023]"}, {"versioned_ensembl_gene_id":"ENSG00000225602.5","gene_symbol":"MTOR-AS1","gene_name":"MTOR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40242]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873935","summary":null,"start":11143898,"end":11149537,"strand":1,"description":"MTOR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40242]"}, {"versioned_ensembl_gene_id":"ENSG00000111679.16","gene_symbol":"PTPN6","gene_name":"protein tyrosine phosphatase, non-receptor type 6 [Source:HGNC Symbol;Acc:HGNC:9658]","synonyms":"SHP1,SHP-1,PTP-1C,HCPH,HCP","biotype":"protein_coding","ncbi_id":"5777","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. N-terminal part of this PTP contains two tandem Src homolog (SH2) domains, which act as protein phospho-tyrosine binding domains, and mediate the interaction of this PTP with its substrates. This PTP is expressed primarily in hematopoietic cells, and functions as an important regulator of multiple signaling pathways in hematopoietic cells. This PTP has been shown to interact with, and dephosphorylate a wide spectrum of phospho-proteins involved in hematopoietic cell signaling. Multiple alternatively spliced variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jul 2008]","start":6946468,"end":6961316,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 6 [Source:HGNC Symbol;Acc:HGNC:9658]"}, {"versioned_ensembl_gene_id":"ENSG00000175395.15","gene_symbol":"ZNF25","gene_name":"zinc finger protein 25 [Source:HGNC Symbol;Acc:HGNC:13043]","synonyms":"Zfp9,KOX19,FLJ31890","biotype":"protein_coding","ncbi_id":"219749","summary":null,"start":37949572,"end":37976633,"strand":-1,"description":"zinc finger protein 25 [Source:HGNC Symbol;Acc:HGNC:13043]"}, {"versioned_ensembl_gene_id":"ENSG00000120217.13","gene_symbol":"CD274","gene_name":"CD274 molecule [Source:HGNC Symbol;Acc:HGNC:17635]","synonyms":"PDL1,PDCD1LG1,PD-L1,B7H1,B7-H1,B7-H","biotype":"protein_coding","ncbi_id":"29126","summary":"This gene encodes an immune inhibitory receptor ligand that is expressed by hematopoietic and non-hematopoietic cells, such as T cells and B cells and various types of tumor cells. The encoded protein is a type I transmembrane protein that has immunoglobulin V-like and C-like domains. Interaction of this ligand with its receptor inhibits T-cell activation and cytokine production. During infection or inflammation of normal tissue, this interaction is important for preventing autoimmunity by maintaining homeostasis of the immune response. In tumor microenvironments, this interaction provides an immune escape for tumor cells through cytotoxic T-cell inactivation. Expression of this gene in tumor cells is considered to be prognostic in many types of human malignancies, including colon cancer and renal cell carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":5450503,"end":5470566,"strand":1,"description":"CD274 molecule [Source:HGNC Symbol;Acc:HGNC:17635]"}, {"versioned_ensembl_gene_id":"ENSG00000146285.13","gene_symbol":"SCML4","gene_name":"sex comb on midleg like 4 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:21397]","synonyms":"dJ47M23.1","biotype":"protein_coding","ncbi_id":"256380","summary":null,"start":107704104,"end":107824317,"strand":-1,"description":"sex comb on midleg like 4 (Drosophila) [Source:HGNC Symbol;Acc:HGNC:21397]"}, {"versioned_ensembl_gene_id":"ENSG00000206396.9","gene_symbol":"MPIG6B","gene_name":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]","synonyms":"C6orf25,G6b-B,G6b,NG31","biotype":"protein_coding","ncbi_id":"80739","summary":"This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":31708815,"end":31716928,"strand":1,"description":"megakaryocyte and platelet inhibitory receptor G6b [Source:HGNC Symbol;Acc:HGNC:13937]"}, {"versioned_ensembl_gene_id":"ENSG00000167553.15","gene_symbol":"TUBA1C","gene_name":"tubulin alpha 1c [Source:HGNC Symbol;Acc:HGNC:20768]","synonyms":"TUBA6,MGC14580,MGC10851,bcm948","biotype":"protein_coding","ncbi_id":"84790","summary":null,"start":49188736,"end":49274603,"strand":1,"description":"tubulin alpha 1c [Source:HGNC Symbol;Acc:HGNC:20768]"}, {"versioned_ensembl_gene_id":"ENSG00000276355.4","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069895,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000241219.1","gene_symbol":"AC078785.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113050912,"end":113063443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135094.10","gene_symbol":"SDS","gene_name":"serine dehydratase [Source:HGNC Symbol;Acc:HGNC:10691]","synonyms":"SDH","biotype":"protein_coding","ncbi_id":"10993","summary":"This gene encodes one of three enzymes that are involved in metabolizing serine and glycine. L-serine dehydratase converts L-serine to pyruvate and ammonia and requires pyridoxal phosphate as a cofactor. The encoded protein can also metabolize threonine to NH4+ and 2-ketobutyrate. The encoded protein is found predominantly in the liver. [provided by RefSeq, Jul 2008]","start":113392445,"end":113426301,"strand":-1,"description":"serine dehydratase [Source:HGNC Symbol;Acc:HGNC:10691]"}, {"versioned_ensembl_gene_id":"ENSG00000240057.5","gene_symbol":"AC078785.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113019532,"end":113183301,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101940.17","gene_symbol":"WDR13","gene_name":"WD repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:14352]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64743","summary":"This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. A similar protein in mouse is thought to be a negative regulator of the pancreatic beta cell proliferation. Mice lacking this gene exhibit increased pancreatic islet mass and higher serum insulin levels, and are mildly obese. [provided by RefSeq, Nov 2016]","start":48590042,"end":48608867,"strand":1,"description":"WD repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:14352]"}, {"versioned_ensembl_gene_id":"ENSG00000272844.1","gene_symbol":"AC074044.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":112990447,"end":112991153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243483.1","gene_symbol":"AC078785.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113041390,"end":113041814,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163607.15","gene_symbol":"GTPBP8","gene_name":"GTP binding protein 8 (putative) [Source:HGNC Symbol;Acc:HGNC:25007]","synonyms":"HSPC135","biotype":"protein_coding","ncbi_id":"29083","summary":null,"start":112990918,"end":113015060,"strand":1,"description":"GTP binding protein 8 (putative) [Source:HGNC Symbol;Acc:HGNC:25007]"}, {"versioned_ensembl_gene_id":"ENSG00000279470.1","gene_symbol":"AC091903.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":51963992,"end":51964445,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248789.5","gene_symbol":"LINC02118","gene_name":"long intergenic non-protein coding RNA 2118 [Source:HGNC Symbol;Acc:HGNC:52974]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105378960","summary":null,"start":52008031,"end":52080987,"strand":1,"description":"long intergenic non-protein coding RNA 2118 [Source:HGNC Symbol;Acc:HGNC:52974]"}, {"versioned_ensembl_gene_id":"ENSG00000253302.1","gene_symbol":"STAU2-AS1","gene_name":"STAU2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44101]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128126","summary":null,"start":73420004,"end":73441526,"strand":1,"description":"STAU2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44101]"}, {"versioned_ensembl_gene_id":"ENSG00000276068.4","gene_symbol":"NAIP","gene_name":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]","synonyms":"NLRB1,BIRC1","biotype":"protein_coding","ncbi_id":"4671","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length; additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":70312214,"end":70368830,"strand":-1,"description":"NLR family apoptosis inhibitory protein [Source:HGNC Symbol;Acc:HGNC:7634]"}, {"versioned_ensembl_gene_id":"ENSG00000215043.2","gene_symbol":"GLULP6","gene_name":"glutamate-ammonia ligase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37990]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"343981","summary":null,"start":194129354,"end":194130266,"strand":-1,"description":"glutamate-ammonia ligase pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37990]"}, {"versioned_ensembl_gene_id":"ENSG00000254273.1","gene_symbol":"AC018620.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73511276,"end":73511654,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258677.2","gene_symbol":"AC022826.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":73688691,"end":73878854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236695.1","gene_symbol":"HNRNPA1P47","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:48777]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287191","summary":null,"start":194187379,"end":194188309,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:48777]"}, {"versioned_ensembl_gene_id":"ENSG00000254538.1","gene_symbol":"AC027018.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73670441,"end":73732897,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236810.5","gene_symbol":"ELOA-AS1","gene_name":"ELOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50582]","synonyms":"TCEB3-AS1","biotype":"antisense_RNA","ncbi_id":"100506963","summary":null,"start":23760382,"end":23778287,"strand":-1,"description":"ELOA antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50582]"}, {"versioned_ensembl_gene_id":"ENSG00000272529.1","gene_symbol":"AC090948.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16345126,"end":16346440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253273.2","gene_symbol":"AC022826.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":73831143,"end":73831947,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131378.13","gene_symbol":"RFTN1","gene_name":"raftlin, lipid raft linker 1 [Source:HGNC Symbol;Acc:HGNC:30278]","synonyms":"Raftlin,MIG2,KIAA0084,FLJ23866","biotype":"protein_coding","ncbi_id":"23180","summary":null,"start":16313574,"end":16514026,"strand":-1,"description":"raftlin, lipid raft linker 1 [Source:HGNC Symbol;Acc:HGNC:30278]"}, {"versioned_ensembl_gene_id":"ENSG00000253383.1","gene_symbol":"AC100784.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73590574,"end":73590883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100450.12","gene_symbol":"GZMH","gene_name":"granzyme H [Source:HGNC Symbol;Acc:HGNC:4710]","synonyms":"CTSGL2,CTLA1,CSP-C,CGL-2,CCP-X","biotype":"protein_coding","ncbi_id":"2999","summary":"This gene encodes a member of the peptidase S1 family of serine proteases. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate a chymotrypsin-like protease. This protein is reported to be constitutively expressed in the NK (natural killer) cells of the immune system and may play a role in the cytotoxic arm of the innate immune response by inducing target cell death and by directly cleaving substrates in pathogen-infected cells. This gene is present in a gene cluster with another member of the granzyme subfamily on chromosome 14. [provided by RefSeq, Nov 2015]","start":24606480,"end":24609699,"strand":-1,"description":"granzyme H [Source:HGNC Symbol;Acc:HGNC:4710]"}, {"versioned_ensembl_gene_id":"ENSG00000205301.11","gene_symbol":"MGAT4D","gene_name":"MGAT4 family member D [Source:HGNC Symbol;Acc:HGNC:43619]","synonyms":"GnT1IP","biotype":"protein_coding","ncbi_id":"152586","summary":null,"start":140442262,"end":140498377,"strand":-1,"description":"MGAT4 family member D [Source:HGNC Symbol;Acc:HGNC:43619]"}, {"versioned_ensembl_gene_id":"ENSG00000005007.12","gene_symbol":"UPF1","gene_name":"UPF1, RNA helicase and ATPase [Source:HGNC Symbol;Acc:HGNC:9962]","synonyms":"smg-2,RENT1,pNORF1,NORF1,KIAA0221,HUPF1","biotype":"protein_coding","ncbi_id":"5976","summary":"This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein is located only in the cytoplasm. When translation ends, it interacts with the protein that is a functional homolog of yeast Upf2p to trigger mRNA decapping. Use of multiple polyadenylation sites has been noted for this gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":18831938,"end":18868236,"strand":1,"description":"UPF1, RNA helicase and ATPase [Source:HGNC Symbol;Acc:HGNC:9962]"}, {"versioned_ensembl_gene_id":"ENSG00000228881.7","gene_symbol":"TRIM26","gene_name":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]","synonyms":"ZNF173,RNF95","biotype":"protein_coding","ncbi_id":"7726","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]","start":30176913,"end":30205889,"strand":-1,"description":"tripartite motif containing 26 [Source:HGNC Symbol;Acc:HGNC:12962]"}, {"versioned_ensembl_gene_id":"ENSG00000215583.3","gene_symbol":"ASS1P6","gene_name":"argininosuccinate synthetase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:769]","synonyms":"ASSP6","biotype":"processed_pseudogene","ncbi_id":"451","summary":null,"start":11922536,"end":11923769,"strand":-1,"description":"argininosuccinate synthetase 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:769]"}, {"versioned_ensembl_gene_id":"ENSG00000226632.1","gene_symbol":"UBE2V1P1","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16581]","synonyms":"dJ687F11.3","biotype":"processed_pseudogene","ncbi_id":"170556","summary":null,"start":3361880,"end":3362324,"strand":-1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16581]"}, {"versioned_ensembl_gene_id":"ENSG00000282047.1","gene_symbol":"TRBVB","gene_name":"T-cell receptor beta variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12248]","synonyms":"TCRBV34S1","biotype":"TR_V_pseudogene","ncbi_id":"28555","summary":null,"start":142752085,"end":142752625,"strand":1,"description":"T-cell receptor beta variable B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:12248]"}, {"versioned_ensembl_gene_id":"ENSG00000263698.1","gene_symbol":"AC012417.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31131456,"end":31132494,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265888.1","gene_symbol":"DSCAS","gene_name":"DSC1/DSC2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51116]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927698","summary":null,"start":31101588,"end":31162789,"strand":1,"description":"DSC1/DSC2 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51116]"}, {"versioned_ensembl_gene_id":"ENSG00000234425.1","gene_symbol":"AL138930.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160537073,"end":160571458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237122.3","gene_symbol":"FAM90A19P","gene_name":"family with sequence similarity 90 member A19, pseudogene [Source:HGNC Symbol;Acc:HGNC:32267]","synonyms":"FAM90A19","biotype":"unprocessed_pseudogene","ncbi_id":"728753","summary":"FAM90A19 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7753682,"end":7756692,"strand":1,"description":"family with sequence similarity 90 member A19, pseudogene [Source:HGNC Symbol;Acc:HGNC:32267]"}, {"versioned_ensembl_gene_id":"ENSG00000280251.1","gene_symbol":"AC091912.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8143618,"end":8143784,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134755.14","gene_symbol":"DSC2","gene_name":"desmocollin 2 [Source:HGNC Symbol;Acc:HGNC:3036]","synonyms":"CDHF2,DSC3","biotype":"protein_coding","ncbi_id":"1824","summary":"This gene encodes a member of the desmocollin protein subfamily. Desmocollins, along with desmogleins, are cadherin-like transmembrane glycoproteins that are major components of the desmosome. Desmosomes are cell-cell junctions that help resist shearing forces and are found in high concentrations in cells subject to mechanical stress. This gene is found in a cluster with other desmocollin family members on chromosome 18. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia-11, and reduced protein expression has been described in several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]","start":31058840,"end":31102415,"strand":-1,"description":"desmocollin 2 [Source:HGNC Symbol;Acc:HGNC:3036]"}, {"versioned_ensembl_gene_id":"ENSG00000249486.1","gene_symbol":"AC091912.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8157541,"end":8157788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273909.1","gene_symbol":"AC138827.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70179769,"end":70181513,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134574.11","gene_symbol":"DDB2","gene_name":"damage specific DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2718]","synonyms":"UV-DDB2,FLJ34321,DDBB,XPE","biotype":"protein_coding","ncbi_id":"1643","summary":"This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":47214465,"end":47239240,"strand":1,"description":"damage specific DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:2718]"}, {"versioned_ensembl_gene_id":"ENSG00000282234.1","gene_symbol":"TRBV27","gene_name":"T-cell receptor beta variable 27 [Source:HGNC Symbol;Acc:HGNC:12208]","synonyms":"TCRBV27S1,TCRBV14S1","biotype":"TR_V_gene","ncbi_id":"28560","summary":null,"start":142756048,"end":142756563,"strand":1,"description":"T-cell receptor beta variable 27 [Source:HGNC Symbol;Acc:HGNC:12208]"}, {"versioned_ensembl_gene_id":"ENSG00000259518.1","gene_symbol":"LINC01583","gene_name":"long intergenic non-protein coding RNA 1583 [Source:HGNC Symbol;Acc:HGNC:51425]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929690","summary":null,"start":82088594,"end":82097694,"strand":1,"description":"long intergenic non-protein coding RNA 1583 [Source:HGNC Symbol;Acc:HGNC:51425]"}, {"versioned_ensembl_gene_id":"ENSG00000272049.1","gene_symbol":"AC091965.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8444949,"end":8445535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123933.16","gene_symbol":"MXD4","gene_name":"MAX dimerization protein 4 [Source:HGNC Symbol;Acc:HGNC:13906]","synonyms":"MSTP149,MST149,MAD4,bHLHc12","biotype":"protein_coding","ncbi_id":"10608","summary":"This gene is a member of the MAD gene family . The MAD genes encode basic helix-loop-helix-leucine zipper proteins that heterodimerize with MAX protein, forming a transcriptional repression complex. The MAD proteins compete for MAX binding with MYC, which heterodimerizes with MAX forming a transcriptional activation complex. Studies in rodents suggest that the MAD genes are tumor suppressors and contribute to the regulation of cell growth in differentiating tissues. [provided by RefSeq, Jul 2008]","start":2247432,"end":2262294,"strand":-1,"description":"MAX dimerization protein 4 [Source:HGNC Symbol;Acc:HGNC:13906]"}, {"versioned_ensembl_gene_id":"ENSG00000245729.2","gene_symbol":"LINC02226","gene_name":"long intergenic non-protein coding RNA 2226 [Source:HGNC Symbol;Acc:HGNC:53095]","synonyms":null,"biotype":"lincRNA","ncbi_id":"729506","summary":null,"start":8333481,"end":8457558,"strand":-1,"description":"long intergenic non-protein coding RNA 2226 [Source:HGNC Symbol;Acc:HGNC:53095]"}, {"versioned_ensembl_gene_id":"ENSG00000235649.2","gene_symbol":"MXRA5Y","gene_name":"matrix remodeling associated 5, Y-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23932]","synonyms":"MXRA5P1,MXRA5P,ADLICANP","biotype":"unprocessed_pseudogene","ncbi_id":"286544","summary":null,"start":11957208,"end":11987386,"strand":1,"description":"matrix remodeling associated 5, Y-linked (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23932]"}, {"versioned_ensembl_gene_id":"ENSG00000231588.1","gene_symbol":"SHQ1P1","gene_name":"SHQ1, H/ACA ribonucleoprotein assembly factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45013]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644451","summary":null,"start":50629532,"end":50631075,"strand":-1,"description":"SHQ1, H/ACA ribonucleoprotein assembly factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45013]"}, {"versioned_ensembl_gene_id":"ENSG00000236477.1","gene_symbol":"RPS24P1","gene_name":"ribosomal protein S24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10412]","synonyms":"RPS24P","biotype":"processed_pseudogene","ncbi_id":"23756","summary":null,"start":12244752,"end":12245457,"strand":1,"description":"ribosomal protein S24 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10412]"}, {"versioned_ensembl_gene_id":"ENSG00000225303.2","gene_symbol":"AL117341.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50472814,"end":50474246,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279863.1","gene_symbol":"AC069547.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":50334538,"end":50336123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248765.1","gene_symbol":"MTCYBP37","gene_name":"mitochondrially encoded cytochrome b pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:52305]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729151","summary":null,"start":8619178,"end":8620310,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:52305]"}, {"versioned_ensembl_gene_id":"ENSG00000279002.1","gene_symbol":"AC091953.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8659764,"end":8660059,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167552.13","gene_symbol":"TUBA1A","gene_name":"tubulin alpha 1a [Source:HGNC Symbol;Acc:HGNC:20766]","synonyms":"TUBA3,FLJ25113,B-ALPHA-1","biotype":"protein_coding","ncbi_id":"7846","summary":"Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. This gene encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blot studies have shown that the gene expression is predominantly found in morphologically differentiated neurologic cells. This gene is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, intellectual disability, and early-onset epilepsy caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]","start":49184796,"end":49189324,"strand":-1,"description":"tubulin alpha 1a [Source:HGNC Symbol;Acc:HGNC:20766]"}, {"versioned_ensembl_gene_id":"ENSG00000198964.13","gene_symbol":"SGMS1","gene_name":"sphingomyelin synthase 1 [Source:HGNC Symbol;Acc:HGNC:29799]","synonyms":"TMEM23,SMS1,MOB,MGC17342","biotype":"protein_coding","ncbi_id":"259230","summary":"The protein encoded by this gene is predicted to be a five-pass transmembrane protein. This gene may be predominately expressed in brain. [provided by RefSeq, Jul 2008]","start":50305586,"end":50625163,"strand":-1,"description":"sphingomyelin synthase 1 [Source:HGNC Symbol;Acc:HGNC:29799]"}, {"versioned_ensembl_gene_id":"ENSG00000247516.6","gene_symbol":"MIR4458HG","gene_name":"MIR4458 host gene [Source:HGNC Symbol;Acc:HGNC:49008]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505738","summary":null,"start":8450743,"end":8463095,"strand":1,"description":"MIR4458 host gene [Source:HGNC Symbol;Acc:HGNC:49008]"}, {"versioned_ensembl_gene_id":"ENSG00000272086.1","gene_symbol":"AC025181.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32174471,"end":32175272,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249159.6","gene_symbol":"AC091965.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8387638,"end":8457564,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279075.1","gene_symbol":"AC091965.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8458842,"end":8459183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260582.1","gene_symbol":"TPST2P1","gene_name":"tyrosylprotein sulfotransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44425]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420710","summary":null,"start":36626674,"end":36627775,"strand":-1,"description":"tyrosylprotein sulfotransferase 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44425]"}, {"versioned_ensembl_gene_id":"ENSG00000169992.9","gene_symbol":"NLGN2","gene_name":"neuroligin 2 [Source:HGNC Symbol;Acc:HGNC:14290]","synonyms":"KIAA1366","biotype":"protein_coding","ncbi_id":"57555","summary":"This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. [provided by RefSeq, Jul 2008]","start":7404874,"end":7419860,"strand":1,"description":"neuroligin 2 [Source:HGNC Symbol;Acc:HGNC:14290]"}, {"versioned_ensembl_gene_id":"ENSG00000251549.2","gene_symbol":"AC091965.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8410789,"end":8410996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250037.1","gene_symbol":"AC091965.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8455946,"end":8456558,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225539.5","gene_symbol":"LINC01821","gene_name":"long intergenic non-protein coding RNA 1821 [Source:HGNC Symbol;Acc:HGNC:52626]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927406","summary":null,"start":194344269,"end":194419645,"strand":1,"description":"long intergenic non-protein coding RNA 1821 [Source:HGNC Symbol;Acc:HGNC:52626]"}, {"versioned_ensembl_gene_id":"ENSG00000259756.1","gene_symbol":"AC100839.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62682916,"end":62690448,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261635.2","gene_symbol":"AC103988.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36613474,"end":36614198,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277631.4","gene_symbol":"PGM5P3-AS1","gene_name":"PGM5P3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51194]","synonyms":"FAM233B","biotype":"lincRNA","ncbi_id":"101929127","summary":null,"start":72674,"end":88826,"strand":1,"description":"PGM5P3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51194]"}, {"versioned_ensembl_gene_id":"ENSG00000253342.1","gene_symbol":"AC009623.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25776679,"end":25777456,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259370.2","gene_symbol":"AC103740.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62827675,"end":62884034,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188765.7","gene_symbol":"TMSB4XP2","gene_name":"thymosin beta 4, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11884]","synonyms":"TMSL2","biotype":"unprocessed_pseudogene","ncbi_id":"7116","summary":null,"start":3617548,"end":3617757,"strand":-1,"description":"thymosin beta 4, X-linked pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:11884]"}, {"versioned_ensembl_gene_id":"ENSG00000236011.6","gene_symbol":"GPANK1","gene_name":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]","synonyms":"D6S54E,GPATCH10,BAT4,G5,ANKRD59","biotype":"protein_coding","ncbi_id":"7918","summary":"This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010]","start":31648638,"end":31653693,"strand":-1,"description":"G-patch domain and ankyrin repeats 1 [Source:HGNC Symbol;Acc:HGNC:13920]"}, {"versioned_ensembl_gene_id":"ENSG00000118004.17","gene_symbol":"COLEC11","gene_name":"collectin subfamily member 11 [Source:HGNC Symbol;Acc:HGNC:17213]","synonyms":"MGC3279,CL-K1","biotype":"protein_coding","ncbi_id":"78989","summary":"This gene encodes a member of the collectin family of C-type lectins that possess collagen-like sequences and carbohydrate recognition domains. Collectins are secreted proteins that play important roles in the innate immune system by binding to carbohydrate antigens on microorganisms, facilitating their recognition and removal. The encoded protein binds to multiple sugars with a preference for fucose and mannose. Mutations in this gene are a cause of 3MC syndrome-2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":3594832,"end":3644644,"strand":1,"description":"collectin subfamily member 11 [Source:HGNC Symbol;Acc:HGNC:17213]"}, {"versioned_ensembl_gene_id":"ENSG00000281830.1","gene_symbol":"LINC01596","gene_name":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]","synonyms":"TCONS_00007705","biotype":"lincRNA","ncbi_id":"105377617","summary":null,"start":189884988,"end":189888341,"strand":1,"description":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]"}, {"versioned_ensembl_gene_id":"ENSG00000280716.1","gene_symbol":"AF250324.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189780336,"end":189899116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185499.16","gene_symbol":"MUC1","gene_name":"mucin 1, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7508]","synonyms":"MCKD,MCD,CD227,ADMCKD1,ADMCKD,PUM,PEM,MCKD1","biotype":"protein_coding","ncbi_id":"4582","summary":"This gene encodes a membrane-bound protein that is a member of the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. This protein is expressed on the apical surface of epithelial cells that line the mucosal surfaces of many different tissues including lung, breast stomach and pancreas. This protein is proteolytically cleaved into alpha and beta subunits that form a heterodimeric complex. The N-terminal alpha subunit functions in cell-adhesion and the C-terminal beta subunit is involved in cell signaling. Overexpression, aberrant intracellular localization, and changes in glycosylation of this protein have been associated with carcinomas. This gene is known to contain a highly polymorphic variable number tandem repeats (VNTR) domain. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]","start":155185824,"end":155192916,"strand":-1,"description":"mucin 1, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7508]"}, {"versioned_ensembl_gene_id":"ENSG00000273245.1","gene_symbol":"AC092653.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73750256,"end":73750786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280997.1","gene_symbol":"CCAT2","gene_name":"colon cancer associated transcript 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:47044]","synonyms":"NCCP1,LINC00873","biotype":"lincRNA","ncbi_id":"101805488","summary":"This gene produces a long non-coding RNA that is upregulated in colon cancer and other cancers. This transcript promotes cell proliferation and suppresses apoptosis. It negatively regulates the biogenesis of microRNA 145. [provided by RefSeq, Dec 2017]","start":127400399,"end":127402150,"strand":1,"description":"colon cancer associated transcript 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:47044]"}, {"versioned_ensembl_gene_id":"ENSG00000090104.11","gene_symbol":"RGS1","gene_name":"regulator of G protein signaling 1 [Source:HGNC Symbol;Acc:HGNC:9991]","synonyms":"1R20,IR20,IER1,BL34","biotype":"protein_coding","ncbi_id":"5996","summary":"This gene encodes a member of the regulator of G-protein signalling family. This protein is located on the cytosolic side of the plasma membrane and contains a conserved, 120 amino acid motif called the RGS domain. The protein attenuates the signalling activity of G-proteins by binding to activated, GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal. [provided by RefSeq, Jul 2008]","start":192575727,"end":192580031,"strand":1,"description":"regulator of G protein signaling 1 [Source:HGNC Symbol;Acc:HGNC:9991]"}, {"versioned_ensembl_gene_id":"ENSG00000229029.2","gene_symbol":"CDCA4P1","gene_name":"cell division cycle associated 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420502","summary":null,"start":14593577,"end":14594200,"strand":1,"description":"cell division cycle associated 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49770]"}, {"versioned_ensembl_gene_id":"ENSG00000280037.1","gene_symbol":"AC092653.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73761269,"end":73761781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189167.11","gene_symbol":"ZAR1L","gene_name":"zygote arrest 1 like [Source:HGNC Symbol;Acc:HGNC:37116]","synonyms":"Z3CXXC7","biotype":"protein_coding","ncbi_id":"646799","summary":"This gene encodes a member of the ZAR1 family that is predominantly expressed in oocytes and early embryos. The protein may function as an RNA regulator in early embryos. [provided by RefSeq, Apr 2010]","start":32303700,"end":32315344,"strand":-1,"description":"zygote arrest 1 like [Source:HGNC Symbol;Acc:HGNC:37116]"}, {"versioned_ensembl_gene_id":"ENSG00000224241.2","gene_symbol":"TMEM183AP1","gene_name":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]","synonyms":"OTTHUMG00000086663,BPG126D10.10","biotype":"processed_pseudogene","ncbi_id":"100048909","summary":null,"start":29577050,"end":29577339,"strand":1,"description":"transmembrane protein 183A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33458]"}, {"versioned_ensembl_gene_id":"ENSG00000175893.11","gene_symbol":"ZDHHC21","gene_name":"zinc finger DHHC-type containing 21 [Source:HGNC Symbol;Acc:HGNC:20750]","synonyms":"HSPC097,DNZ1,DHHC21","biotype":"protein_coding","ncbi_id":"340481","summary":null,"start":14611071,"end":14693471,"strand":-1,"description":"zinc finger DHHC-type containing 21 [Source:HGNC Symbol;Acc:HGNC:20750]"}, {"versioned_ensembl_gene_id":"ENSG00000231464.1","gene_symbol":"AC024937.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":195996738,"end":195998233,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166881.9","gene_symbol":"NEMP1","gene_name":"nuclear envelope integral membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29001]","synonyms":"TMEM194A,TMEM194,KIAA0286","biotype":"protein_coding","ncbi_id":"23306","summary":null,"start":57055643,"end":57088063,"strand":-1,"description":"nuclear envelope integral membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:29001]"}, {"versioned_ensembl_gene_id":"ENSG00000227917.2","gene_symbol":"AL449043.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":100804,"end":102941,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224654.2","gene_symbol":"UBD","gene_name":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]","synonyms":"FAT10","biotype":"protein_coding","ncbi_id":"10537","summary":"This gene encodes a protein which contains two ubiquitin-like domains and appears to have similar function to ubiquitin. Through covalent attachment, the encoded protein targets other proteins for 26S proteasome degradation. This protein has been implicated to function in many cellular processes, including caspase-dependent apoptosis, formation of aggresomes, mitotic regulation, and dendritic cell maturation. Upregulation of this gene may promote inflammation in chronic kidney disease and has been observed in many cancer types. [provided by RefSeq, Aug 2017]","start":29555178,"end":29559492,"strand":-1,"description":"ubiquitin D [Source:HGNC Symbol;Acc:HGNC:18795]"}, {"versioned_ensembl_gene_id":"ENSG00000231808.2","gene_symbol":"LINC01388","gene_name":"long intergenic non-protein coding RNA 1388 [Source:HGNC Symbol;Acc:HGNC:50660]","synonyms":"TCONS_l2_00029888","biotype":"lincRNA","ncbi_id":"101929179","summary":null,"start":112713,"end":113754,"strand":-1,"description":"long intergenic non-protein coding RNA 1388 [Source:HGNC Symbol;Acc:HGNC:50660]"}, {"versioned_ensembl_gene_id":"ENSG00000249782.1","gene_symbol":"AC027328.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8525179,"end":8528679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260613.1","gene_symbol":"Z98885.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49832616,"end":49837786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170122.5","gene_symbol":"FOXD4","gene_name":"forkhead box D4 [Source:HGNC Symbol;Acc:HGNC:3805]","synonyms":"FREAC5,FOXD4a,FKHL9","biotype":"protein_coding","ncbi_id":"2298","summary":"This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. Mutations in this gene are associated with a complex phenotype consisting of dilated cardiomyopathy, obsessive-compulsive disorders, and suicidality. [provided by RefSeq, Mar 2012]","start":116231,"end":118204,"strand":-1,"description":"forkhead box D4 [Source:HGNC Symbol;Acc:HGNC:3805]"}, {"versioned_ensembl_gene_id":"ENSG00000229409.1","gene_symbol":"AL117328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49845929,"end":49846090,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279097.1","gene_symbol":"AC091953.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8572047,"end":8572206,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279494.1","gene_symbol":"AL117328.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49851425,"end":49853364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280451.1","gene_symbol":"AL356094.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":93811825,"end":93813036,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231608.9","gene_symbol":"TNXB","gene_name":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]","synonyms":"TNXBS,XBS,TNXB1,XB,TNXB2","biotype":"protein_coding","ncbi_id":"7148","summary":"This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32016970,"end":32093383,"strand":-1,"description":"tenascin XB [Source:HGNC Symbol;Acc:HGNC:11976]"}, {"versioned_ensembl_gene_id":"ENSG00000279264.1","gene_symbol":"AC091953.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8614356,"end":8614696,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230829.3","gene_symbol":"AC025181.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32221932,"end":32222347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225728.2","gene_symbol":"AL034399.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107939263,"end":107939642,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250389.1","gene_symbol":"MTND6P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39465]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478941","summary":null,"start":8618581,"end":8619104,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39465]"}, {"versioned_ensembl_gene_id":"ENSG00000147869.4","gene_symbol":"CER1","gene_name":"cerberus 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:1862]","synonyms":"DAND4","biotype":"protein_coding","ncbi_id":"9350","summary":"This gene encodes a cytokine member of the cysteine knot superfamily, characterized by nine conserved cysteines and a cysteine knot region. The cerberus-related cytokines, together with Dan and DRM/Gremlin, represent a group of bone morphogenetic protein (BMP) antagonists that can bind directly to BMPs and inhibit their activity. [provided by RefSeq, Jul 2008]","start":14719724,"end":14722717,"strand":-1,"description":"cerberus 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:1862]"}, {"versioned_ensembl_gene_id":"ENSG00000100426.6","gene_symbol":"ZBED4","gene_name":"zinc finger BED-type containing 4 [Source:HGNC Symbol;Acc:HGNC:20721]","synonyms":"KIAA0637","biotype":"protein_coding","ncbi_id":"9889","summary":null,"start":49853842,"end":49890078,"strand":1,"description":"zinc finger BED-type containing 4 [Source:HGNC Symbol;Acc:HGNC:20721]"}, {"versioned_ensembl_gene_id":"ENSG00000280373.1","gene_symbol":"AC091953.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8669018,"end":8669250,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223656.1","gene_symbol":"HMGB3P10","gene_name":"high mobility group box 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39302]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129320","summary":null,"start":99698242,"end":99699178,"strand":1,"description":"high mobility group box 3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39302]"}, {"versioned_ensembl_gene_id":"ENSG00000204954.9","gene_symbol":"C12orf73","gene_name":"chromosome 12 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:34450]","synonyms":"FLJ13975,DKFZp547P055","biotype":"protein_coding","ncbi_id":"728568","summary":null,"start":103950202,"end":103965708,"strand":-1,"description":"chromosome 12 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:34450]"}, {"versioned_ensembl_gene_id":"ENSG00000144048.10","gene_symbol":"DUSP11","gene_name":"dual specificity phosphatase 11 [Source:HGNC Symbol;Acc:HGNC:3066]","synonyms":"PIR1","biotype":"protein_coding","ncbi_id":"8446","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product is localized to the nucleus and binds directly to RNA and splicing factors, and thus it is suggested to participate in nuclear mRNA metabolism. [provided by RefSeq, Sep 2008]","start":73762184,"end":73780157,"strand":-1,"description":"dual specificity phosphatase 11 [Source:HGNC Symbol;Acc:HGNC:3066]"}, {"versioned_ensembl_gene_id":"ENSG00000101298.13","gene_symbol":"SNPH","gene_name":"syntaphilin [Source:HGNC Symbol;Acc:HGNC:15931]","synonyms":"bA314N13.5","biotype":"protein_coding","ncbi_id":"9751","summary":"Syntaxin-1, synaptobrevin/VAMP, and SNAP25 interact to form the SNARE complex, which is required for synaptic vesicle docking and fusion. The protein encoded by this gene is membrane-associated and inhibits SNARE complex formation by binding free syntaxin-1. Expression of this gene appears to be brain-specific. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":1266316,"end":1309328,"strand":1,"description":"syntaphilin [Source:HGNC Symbol;Acc:HGNC:15931]"}, {"versioned_ensembl_gene_id":"ENSG00000235059.5","gene_symbol":"AC008175.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22438940,"end":22485592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117090.14","gene_symbol":"SLAMF1","gene_name":"signaling lymphocytic activation molecule family member 1 [Source:HGNC Symbol;Acc:HGNC:10903]","synonyms":"SLAM,CD150","biotype":"protein_coding","ncbi_id":"6504","summary":null,"start":160608100,"end":160647295,"strand":-1,"description":"signaling lymphocytic activation molecule family member 1 [Source:HGNC Symbol;Acc:HGNC:10903]"}, {"versioned_ensembl_gene_id":"ENSG00000227044.4","gene_symbol":"OR2H2","gene_name":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]","synonyms":"hs6M1-12","biotype":"protein_coding","ncbi_id":"7932","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29587046,"end":29588629,"strand":1,"description":"olfactory receptor family 2 subfamily H member 2 [Source:HGNC Symbol;Acc:HGNC:8253]"}, {"versioned_ensembl_gene_id":"ENSG00000131538.7","gene_symbol":"TTTY6","gene_name":"testis-specific transcript, Y-linked 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16483]","synonyms":"TTY6,TTTY6A,LINC00127","biotype":"lincRNA","ncbi_id":"84672","summary":"There are two copies of this locus in the P3 palindrome on chromosome Y. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":22439593,"end":22441458,"strand":-1,"description":"testis-specific transcript, Y-linked 6 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16483]"}, {"versioned_ensembl_gene_id":"ENSG00000117507.6","gene_symbol":"FMO6P","gene_name":"flavin containing monooxygenase 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:24024]","synonyms":"FMO6","biotype":"transcribed_unitary_pseudogene","ncbi_id":"388714","summary":null,"start":171137740,"end":171161568,"strand":1,"description":"flavin containing monooxygenase 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:24024]"}, {"versioned_ensembl_gene_id":"ENSG00000277883.1","gene_symbol":"NLRP3P1","gene_name":"NLR family pyrin domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29886]","synonyms":"NOD13,NLRP3P","biotype":"unprocessed_pseudogene","ncbi_id":"347402","summary":null,"start":107974078,"end":107985008,"strand":1,"description":"NLR family pyrin domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29886]"}, {"versioned_ensembl_gene_id":"ENSG00000253924.1","gene_symbol":"AC103831.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52294455,"end":52301942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170925.3","gene_symbol":"TEX13B","gene_name":"testis expressed 13B [Source:HGNC Symbol;Acc:HGNC:11736]","synonyms":"TSGA5,TGC3B","biotype":"protein_coding","ncbi_id":"56156","summary":"This gene is similar to a mouse gene that is expressed in the testis. [provided by RefSeq, Jul 2008]","start":107980864,"end":107982370,"strand":-1,"description":"testis expressed 13B [Source:HGNC Symbol;Acc:HGNC:11736]"}, {"versioned_ensembl_gene_id":"ENSG00000253551.1","gene_symbol":"AC021915.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52194362,"end":52199580,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258232.2","gene_symbol":"AC125611.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49265156,"end":49273306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235334.1","gene_symbol":"BTG3P1","gene_name":"BTG anti-proliferation factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51543]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419246","summary":null,"start":128122734,"end":128123496,"strand":1,"description":"BTG anti-proliferation factor 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51543]"}, {"versioned_ensembl_gene_id":"ENSG00000271559.1","gene_symbol":"AL138966.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26229332,"end":26229644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225034.2","gene_symbol":"BX927223.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29573499,"end":29574426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227882.1","gene_symbol":"THAP12P6","gene_name":"THAP domain containing 12 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39570]","synonyms":"PRKRIRP6","biotype":"processed_pseudogene","ncbi_id":"100128764","summary":null,"start":26234213,"end":26237129,"strand":1,"description":"THAP domain containing 12 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39570]"}, {"versioned_ensembl_gene_id":"ENSG00000035499.12","gene_symbol":"DEPDC1B","gene_name":"DEP domain containing 1B [Source:HGNC Symbol;Acc:HGNC:24902]","synonyms":"XTP1,BRCC3","biotype":"protein_coding","ncbi_id":"55789","summary":null,"start":60596912,"end":60700190,"strand":-1,"description":"DEP domain containing 1B [Source:HGNC Symbol;Acc:HGNC:24902]"}, {"versioned_ensembl_gene_id":"ENSG00000169255.13","gene_symbol":"B3GALNT1","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) [Source:HGNC Symbol;Acc:HGNC:918]","synonyms":"P1,GLOB,galT3,beta3Gal-T3,B3GALT3","biotype":"protein_coding","ncbi_id":"8706","summary":"This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). The encoded protein of this gene does not use N-acetylglucosamine as an acceptor sugar at all. [provided by RefSeq, Mar 2017]","start":161083883,"end":161105384,"strand":-1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) [Source:HGNC Symbol;Acc:HGNC:918]"}, {"versioned_ensembl_gene_id":"ENSG00000134317.17","gene_symbol":"GRHL1","gene_name":"grainyhead like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:17923]","synonyms":"TFCP2L2,MGR,LBP-32","biotype":"protein_coding","ncbi_id":"29841","summary":"This gene encodes a member of the grainyhead family of transcription factors. The encoded protein can exist as a homodimer or can form heterodimers with sister-of-mammalian grainyhead or brother-of-mammalian grainyhead. This protein functions as a transcription factor during development. [provided by RefSeq, Jun 2009]","start":9951693,"end":10002277,"strand":1,"description":"grainyhead like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:17923]"}, {"versioned_ensembl_gene_id":"ENSG00000269228.1","gene_symbol":"RPS27AP19","gene_name":"ribosomal protein S27a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52298]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107985274","summary":null,"start":7665717,"end":7666476,"strand":1,"description":"ribosomal protein S27a pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:52298]"}, {"versioned_ensembl_gene_id":"ENSG00000273192.1","gene_symbol":"AL671710.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49902228,"end":49904576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271156.1","gene_symbol":"AC090578.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88808318,"end":88808908,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278165.3","gene_symbol":"DUSP8","gene_name":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]","synonyms":"FLJ42958,C11orf81,HVH-5,HB5","biotype":"protein_coding","ncbi_id":"1850","summary":"The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates SAPK/JNK and p38, is expressed predominantly in the adult brain, heart, and skeletal muscle, is localized in the cytoplasm, and is induced by nerve growth factor and insulin. An intronless pseudogene for DUSP8 is present on chromosome 10q11.2. [provided by RefSeq, Jul 2008]","start":1554044,"end":1571920,"strand":-1,"description":"dual specificity phosphatase 8 [Source:HGNC Symbol;Acc:HGNC:3074]"}, {"versioned_ensembl_gene_id":"ENSG00000243485.5","gene_symbol":"MIR1302-2HG","gene_name":"MIR1302-2 host gene [Source:HGNC Symbol;Acc:HGNC:52482]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985730","summary":null,"start":29554,"end":31109,"strand":1,"description":"MIR1302-2 host gene [Source:HGNC Symbol;Acc:HGNC:52482]"}, {"versioned_ensembl_gene_id":"ENSG00000224146.1","gene_symbol":"BX927223.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29582099,"end":29582616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101842.13","gene_symbol":"VSIG1","gene_name":"V-set and immunoglobulin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28675]","synonyms":"MGC44287","biotype":"protein_coding","ncbi_id":"340547","summary":"This gene encodes a member of the junctional adhesion molecule (JAM) family. The encoded protein contains multiple glycosylation sites at the N-terminal region, and multiple phosphorylation sites and glutamic acid/proline (EP) repeats at the C-terminal region. The gene is expressed in normal stomach and testis, as well as in gastric, esophageal and ovarian cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":108044970,"end":108079184,"strand":1,"description":"V-set and immunoglobulin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28675]"}, {"versioned_ensembl_gene_id":"ENSG00000223972.5","gene_symbol":"DDX11L1","gene_name":"DEAD/H-box helicase 11 like 1 [Source:HGNC Symbol;Acc:HGNC:37102]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100287102","summary":null,"start":11869,"end":14409,"strand":1,"description":"DEAD/H-box helicase 11 like 1 [Source:HGNC Symbol;Acc:HGNC:37102]"}, {"versioned_ensembl_gene_id":"ENSG00000226200.6","gene_symbol":"SGMS1-AS1","gene_name":"SGMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49683]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355295","summary":null,"start":50624951,"end":50641451,"strand":1,"description":"SGMS1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:49683]"}, {"versioned_ensembl_gene_id":"ENSG00000111087.9","gene_symbol":"GLI1","gene_name":"GLI family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:4317]","synonyms":"GLI","biotype":"protein_coding","ncbi_id":"2735","summary":"This gene encodes a member of the Kruppel family of zinc finger proteins. The encoded transcription factor is activated by the sonic hedgehog signal transduction cascade and regulates stem cell proliferation. The activity and nuclear localization of this protein is negatively regulated by p53 in an inhibitory loop. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]","start":57460135,"end":57472262,"strand":1,"description":"GLI family zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:4317]"}, {"versioned_ensembl_gene_id":"ENSG00000227232.5","gene_symbol":"WASH7P","gene_name":"WAS protein family homolog 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:38034]","synonyms":"FAM39F","biotype":"unprocessed_pseudogene","ncbi_id":"653635","summary":null,"start":14404,"end":29570,"strand":-1,"description":"WAS protein family homolog 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:38034]"}, {"versioned_ensembl_gene_id":"ENSG00000244588.5","gene_symbol":"RAD21L1","gene_name":"RAD21 cohesin complex component like 1 [Source:HGNC Symbol;Acc:HGNC:16271]","synonyms":"RAD21L,dJ545L17.2","biotype":"protein_coding","ncbi_id":"642636","summary":null,"start":1226056,"end":1296421,"strand":1,"description":"RAD21 cohesin complex component like 1 [Source:HGNC Symbol;Acc:HGNC:16271]"}, {"versioned_ensembl_gene_id":"ENSG00000274654.1","gene_symbol":"AC022467.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":48528980,"end":48529728,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156219.16","gene_symbol":"ART3","gene_name":"ADP-ribosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:725]","synonyms":null,"biotype":"protein_coding","ncbi_id":"419","summary":"This gene encodes an arginine-specific ADP-ribosyltransferase. The encoded protein catalyzes a reversible reaction which modifies proteins by the addition or removal of ADP-ribose to an arginine residue to regulate the function of the modified protein. An ADP-ribosyltransferase pseudogene is located on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":76011184,"end":76112802,"strand":1,"description":"ADP-ribosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:725]"}, {"versioned_ensembl_gene_id":"ENSG00000166147.13","gene_symbol":"FBN1","gene_name":"fibrillin 1 [Source:HGNC Symbol;Acc:HGNC:3603]","synonyms":"FBN,WMS,SGS,OCTD,MFS1,MASS","biotype":"protein_coding","ncbi_id":"2200","summary":"This gene encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin. Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils. These microfibrils provide force-bearing structural support in elastic and nonelastic connective tissue throughout the body. Asprosin, secreted by white adipose tissue, has been shown to regulate glucose homeostasis. Mutations in this gene are associated with Marfan syndrome and the related MASS phenotype, as well as ectopia lentis syndrome, Weill-Marchesani syndrome, Shprintzen-Goldberg syndrome and neonatal progeroid syndrome. [provided by RefSeq, Apr 2016]","start":48408306,"end":48645849,"strand":-1,"description":"fibrillin 1 [Source:HGNC Symbol;Acc:HGNC:3603]"}, {"versioned_ensembl_gene_id":"ENSG00000148600.14","gene_symbol":"CDHR1","gene_name":"cadherin related family member 1 [Source:HGNC Symbol;Acc:HGNC:14550]","synonyms":"RP65,PCDH21,KIAA1775,CORD15","biotype":"protein_coding","ncbi_id":"92211","summary":"This gene belongs to the cadherin superfamily of calcium-dependent cell adhesion molecules. The encoded protein is a photoreceptor-specific cadherin that plays a role in outer segment disc morphogenesis. Mutations in this gene are associated with inherited retinal dystrophies. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2013]","start":84194635,"end":84219621,"strand":1,"description":"cadherin related family member 1 [Source:HGNC Symbol;Acc:HGNC:14550]"}, {"versioned_ensembl_gene_id":"ENSG00000281176.1","gene_symbol":"KRTAP5-AS1","gene_name":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"338651","summary":null,"start":1571353,"end":1599200,"strand":1,"description":"KRTAP5-1/KRTAP5-2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27877]"}, {"versioned_ensembl_gene_id":"ENSG00000280585.1","gene_symbol":"KRTAP5-1","gene_name":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]","synonyms":"KRTAP5.1,KRN1L","biotype":"protein_coding","ncbi_id":"387264","summary":null,"start":1584352,"end":1585293,"strand":-1,"description":"keratin associated protein 5-1 [Source:HGNC Symbol;Acc:HGNC:23596]"}, {"versioned_ensembl_gene_id":"ENSG00000137460.8","gene_symbol":"FHDC1","gene_name":"FH2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29363]","synonyms":"KIAA1727","biotype":"protein_coding","ncbi_id":"85462","summary":null,"start":152936352,"end":152979696,"strand":1,"description":"FH2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29363]"}, {"versioned_ensembl_gene_id":"ENSG00000281533.1","gene_symbol":"KRTAP5-2","gene_name":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]","synonyms":"KRTAP5.2,KRTAP5-8","biotype":"protein_coding","ncbi_id":"440021","summary":null,"start":1597193,"end":1598310,"strand":-1,"description":"keratin associated protein 5-2 [Source:HGNC Symbol;Acc:HGNC:23597]"}, {"versioned_ensembl_gene_id":"ENSG00000115808.11","gene_symbol":"STRN","gene_name":"striatin [Source:HGNC Symbol;Acc:HGNC:11424]","synonyms":"STRN1,PPP2R6A","biotype":"protein_coding","ncbi_id":"6801","summary":null,"start":36843640,"end":36966472,"strand":-1,"description":"striatin [Source:HGNC Symbol;Acc:HGNC:11424]"}, {"versioned_ensembl_gene_id":"ENSG00000253929.1","gene_symbol":"CASC21","gene_name":"cancer susceptibility 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49836]","synonyms":"LINC01244,CARLo-2","biotype":"lincRNA","ncbi_id":"103021164","summary":null,"start":127339274,"end":127392631,"strand":1,"description":"cancer susceptibility 21 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49836]"}, {"versioned_ensembl_gene_id":"ENSG00000184164.14","gene_symbol":"CRELD2","gene_name":"cysteine rich with EGF like domains 2 [Source:HGNC Symbol;Acc:HGNC:28150]","synonyms":"MGC11256","biotype":"protein_coding","ncbi_id":"79174","summary":null,"start":49918167,"end":49927540,"strand":1,"description":"cysteine rich with EGF like domains 2 [Source:HGNC Symbol;Acc:HGNC:28150]"}, {"versioned_ensembl_gene_id":"ENSG00000092199.17","gene_symbol":"HNRNPC","gene_name":"heterogeneous nuclear ribonucleoprotein C (C1/C2) [Source:HGNC Symbol;Acc:HGNC:5035]","synonyms":"HNRPC,hnRNPC","biotype":"protein_coding","ncbi_id":"3183","summary":"This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene can act as a tetramer and is involved in the assembly of 40S hnRNP particles. Multiple transcript variants encoding at least two different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":21209136,"end":21269494,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C (C1/C2) [Source:HGNC Symbol;Acc:HGNC:5035]"}, {"versioned_ensembl_gene_id":"ENSG00000279125.1","gene_symbol":"AC091953.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8685581,"end":8685816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282160.1","gene_symbol":"AF067845.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1373685,"end":1381394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282692.1","gene_symbol":"AC129915.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1018757,"end":1019704,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282375.1","gene_symbol":"AC100797.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":738548,"end":740374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230947.2","gene_symbol":"AP000356.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":24598054,"end":24599398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271509.1","gene_symbol":"AC018714.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127292233,"end":127292440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253267.5","gene_symbol":"DLGAP2-AS1","gene_name":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507435","summary":null,"start":1565509,"end":1622417,"strand":-1,"description":"DLGAP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50467]"}, {"versioned_ensembl_gene_id":"ENSG00000281961.1","gene_symbol":"AF067845.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1377867,"end":1380307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282759.1","gene_symbol":"AC026950.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":891251,"end":893112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254160.1","gene_symbol":"AC110288.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1246789,"end":1248760,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000212993.4","gene_symbol":"POU5F1B","gene_name":"POU class 5 homeobox 1B [Source:HGNC Symbol;Acc:HGNC:9223]","synonyms":"POU5F1P1,OTF3P1,OTF3C","biotype":"protein_coding","ncbi_id":"5462","summary":"This intronless gene was thought to be a transcribed pseudogene of POU class 5 homeobox 1, however, it has been reported that this gene can encode a functional protein. The encoded protein is nearly the same length as and highly similar to the POU class 5 homeobox 1 transcription factor, has been shown to be a weak transcriptional activator and may play a role in carcinogenesis and eye development. [provided by RefSeq, Apr 2009]","start":127414290,"end":127420069,"strand":1,"description":"POU class 5 homeobox 1B [Source:HGNC Symbol;Acc:HGNC:9223]"}, {"versioned_ensembl_gene_id":"ENSG00000275427.1","gene_symbol":"AF067845.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1296034,"end":1302607,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100031.18","gene_symbol":"GGT1","gene_name":"gamma-glutamyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4250]","synonyms":"CD224,GGT,D22S732,D22S672","biotype":"protein_coding","ncbi_id":"2678","summary":"The enzyme encoded by this gene is a type I gamma-glutamyltransferase that catalyzes the transfer of the glutamyl moiety of glutathione to a variety of amino acids and dipeptide acceptors. The enzyme is composed of a heavy chain and a light chain, which are derived from a single precursor protein. It is expressed in tissues involved in absorption and secretion and may contribute to the etiology of diabetes and other metabolic disorders. Multiple alternatively spliced variants have been identified. There are a number of related genes present on chromosomes 20 and 22, and putative pseudogenes for this gene on chromosomes 2, 13, and 22. [provided by RefSeq, Jan 2014]","start":24583750,"end":24629005,"strand":1,"description":"gamma-glutamyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:4250]"}, {"versioned_ensembl_gene_id":"ENSG00000228863.8","gene_symbol":"AL121985.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":160670778,"end":160699761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225556.1","gene_symbol":"C2CD4D","gene_name":"C2 calcium dependent domain containing 4D [Source:HGNC Symbol;Acc:HGNC:37210]","synonyms":"FAM148D","biotype":"protein_coding","ncbi_id":"100191040","summary":null,"start":151837819,"end":151840557,"strand":-1,"description":"C2 calcium dependent domain containing 4D [Source:HGNC Symbol;Acc:HGNC:37210]"}, {"versioned_ensembl_gene_id":"ENSG00000104714.13","gene_symbol":"ERICH1","gene_name":"glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:27234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"157697","summary":null,"start":614746,"end":738106,"strand":-1,"description":"glutamate rich 1 [Source:HGNC Symbol;Acc:HGNC:27234]"}, {"versioned_ensembl_gene_id":"ENSG00000215515.2","gene_symbol":"IFIT1P1","gene_name":"interferon induced protein with tetratricopeptide repeats 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5408]","synonyms":"II56P,IFIT1P,IFI56P,G13P1","biotype":"processed_pseudogene","ncbi_id":"8373","summary":null,"start":32384660,"end":32386108,"strand":1,"description":"interferon induced protein with tetratricopeptide repeats 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:5408]"}, {"versioned_ensembl_gene_id":"ENSG00000234614.1","gene_symbol":"AL450992.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151841877,"end":151850385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139618.14","gene_symbol":"BRCA2","gene_name":"BRCA2, DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1101]","synonyms":"FACD,BRCC2,XRCC11,FANCD1,FANCD,FAD1,FAD","biotype":"protein_coding","ncbi_id":"675","summary":"Inherited mutations in BRCA1 and this gene, BRCA2, confer increased lifetime risk of developing breast or ovarian cancer. Both BRCA1 and BRCA2 are involved in maintenance of genome stability, specifically the homologous recombination pathway for double-strand DNA repair. The largest exon in both genes is exon 11, which harbors the most important and frequent mutations in breast cancer patients. The BRCA2 gene was found on chromosome 13q12.3 in human. The BRCA2 protein contains several copies of a 70 aa motif called the BRC motif, and these motifs mediate binding to the RAD51 recombinase which functions in DNA repair. BRCA2 is considered a tumor suppressor gene, as tumors with BRCA2 mutations generally exhibit loss of heterozygosity (LOH) of the wild-type allele. [provided by RefSeq, May 2020]","start":32315474,"end":32400266,"strand":1,"description":"BRCA2, DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1101]"}, {"versioned_ensembl_gene_id":"ENSG00000196407.11","gene_symbol":"THEM5","gene_name":"thioesterase superfamily member 5 [Source:HGNC Symbol;Acc:HGNC:26755]","synonyms":"FLJ37964","biotype":"protein_coding","ncbi_id":"284486","summary":null,"start":151847263,"end":151853697,"strand":-1,"description":"thioesterase superfamily member 5 [Source:HGNC Symbol;Acc:HGNC:26755]"}, {"versioned_ensembl_gene_id":"ENSG00000149609.5","gene_symbol":"C20orf144","gene_name":"chromosome 20 open reading frame 144 [Source:HGNC Symbol;Acc:HGNC:16137]","synonyms":"dJ63M2.6,bclt","biotype":"protein_coding","ncbi_id":"128864","summary":null,"start":33662284,"end":33665619,"strand":1,"description":"chromosome 20 open reading frame 144 [Source:HGNC Symbol;Acc:HGNC:16137]"}, {"versioned_ensembl_gene_id":"ENSG00000117091.9","gene_symbol":"CD48","gene_name":"CD48 molecule [Source:HGNC Symbol;Acc:HGNC:1683]","synonyms":"SLAMF2,mCD48,hCD48,BLAST,BCM1","biotype":"protein_coding","ncbi_id":"962","summary":"This gene encodes a member of the CD2 subfamily of immunoglobulin-like receptors which includes SLAM (signaling lymphocyte activation molecules) proteins. The encoded protein is found on the surface of lymphocytes and other immune cells, dendritic cells and endothelial cells, and participates in activation and differentiation pathways in these cells. The encoded protein does not have a transmembrane domain, however, but is held at the cell surface by a GPI anchor via a C-terminal domain which maybe cleaved to yield a soluble form of the receptor. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]","start":160678746,"end":160711851,"strand":-1,"description":"CD48 molecule [Source:HGNC Symbol;Acc:HGNC:1683]"}, {"versioned_ensembl_gene_id":"ENSG00000246228.6","gene_symbol":"CASC8","gene_name":"cancer susceptibility 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:45129]","synonyms":"LINC00860,CARLo-1","biotype":"antisense_RNA","ncbi_id":"727677","summary":null,"start":127289817,"end":127482139,"strand":-1,"description":"cancer susceptibility 8 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:45129]"}, {"versioned_ensembl_gene_id":"ENSG00000249022.1","gene_symbol":"AC093599.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":153034211,"end":153091165,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236798.1","gene_symbol":"CR788282.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30179256,"end":30181079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182584.4","gene_symbol":"ACTL10","gene_name":"actin like 10 [Source:HGNC Symbol;Acc:HGNC:16127]","synonyms":"C20orf134","biotype":"protein_coding","ncbi_id":"170487","summary":null,"start":33666498,"end":33668525,"strand":1,"description":"actin like 10 [Source:HGNC Symbol;Acc:HGNC:16127]"}, {"versioned_ensembl_gene_id":"ENSG00000241713.7","gene_symbol":"LY6G5B","gene_name":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]","synonyms":"C6orf19,G5b","biotype":"protein_coding","ncbi_id":"58496","summary":"LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31656528,"end":31660956,"strand":1,"description":"lymphocyte antigen 6 family member G5B [Source:HGNC Symbol;Acc:HGNC:13931]"}, {"versioned_ensembl_gene_id":"ENSG00000258123.1","gene_symbol":"LINC02444","gene_name":"long intergenic non-protein coding RNA 2444 [Source:HGNC Symbol;Acc:HGNC:53376]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928137","summary":null,"start":73159190,"end":73208317,"strand":1,"description":"long intergenic non-protein coding RNA 2444 [Source:HGNC Symbol;Acc:HGNC:53376]"}, {"versioned_ensembl_gene_id":"ENSG00000132825.6","gene_symbol":"PPP1R3D","gene_name":"protein phosphatase 1 regulatory subunit 3D [Source:HGNC Symbol;Acc:HGNC:9294]","synonyms":"PPP1R6","biotype":"protein_coding","ncbi_id":"5509","summary":"Phosphorylation of serine and threonine residues in proteins is a crucial step in the regulation of many cellular functions ranging from hormonal regulation to cell division and even short-term memory. The level of phosphorylation is controlled by the opposing actions of protein kinases and protein phosphatases. Protein phosphatase 1 (PP1) is 1 of 4 major serine/threonine-specific protein phosphatases which have been identified in eukaryotic cells. PP1 associates with various regulatory subunits that dictate its subcellular localization and modulate its substrate specificity. Several subunits that target PP1 to glycogen have been identified. This gene encodes a glycogen-targeting subunit of PP1. [provided by RefSeq, Jul 2008]","start":59936668,"end":59940297,"strand":-1,"description":"protein phosphatase 1 regulatory subunit 3D [Source:HGNC Symbol;Acc:HGNC:9294]"}, {"versioned_ensembl_gene_id":"ENSG00000257682.1","gene_symbol":"AC090503.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73203815,"end":73206835,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172243.17","gene_symbol":"CLEC7A","gene_name":"C-type lectin domain containing 7A [Source:HGNC Symbol;Acc:HGNC:14558]","synonyms":"dectin-1,CLECSF12,CD369,SCARE2,hDectin-1","biotype":"protein_coding","ncbi_id":"64581","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with an immunoreceptor tyrosine-based activation motif. It functions as a pattern-recognition receptor that recognizes a variety of beta-1,3-linked and beta-1,6-linked glucans from fungi and plants, and in this way plays a role in innate immune response. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]","start":10116777,"end":10130258,"strand":-1,"description":"C-type lectin domain containing 7A [Source:HGNC Symbol;Acc:HGNC:14558]"}, {"versioned_ensembl_gene_id":"ENSG00000114554.11","gene_symbol":"PLXNA1","gene_name":"plexin A1 [Source:HGNC Symbol;Acc:HGNC:9099]","synonyms":"PLXN1,NOV","biotype":"protein_coding","ncbi_id":"5361","summary":null,"start":126988594,"end":127037392,"strand":1,"description":"plexin A1 [Source:HGNC Symbol;Acc:HGNC:9099]"}, {"versioned_ensembl_gene_id":"ENSG00000235101.1","gene_symbol":"SETP9","gene_name":"SET pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42928]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100129738","summary":null,"start":160670148,"end":160670979,"strand":1,"description":"SET pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42928]"}, {"versioned_ensembl_gene_id":"ENSG00000196227.10","gene_symbol":"FAM217B","gene_name":"family with sequence similarity 217 member B [Source:HGNC Symbol;Acc:HGNC:16170]","synonyms":"dJ551D2.5,C20orf177","biotype":"protein_coding","ncbi_id":"63939","summary":null,"start":59933764,"end":59948680,"strand":1,"description":"family with sequence similarity 217 member B [Source:HGNC Symbol;Acc:HGNC:16170]"}, {"versioned_ensembl_gene_id":"ENSG00000214198.8","gene_symbol":"TTC41P","gene_name":"tetratricopeptide repeat domain 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:49210]","synonyms":"GNNP","biotype":"transcribed_unitary_pseudogene","ncbi_id":"253724","summary":null,"start":103843749,"end":103930211,"strand":-1,"description":"tetratricopeptide repeat domain 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:49210]"}, {"versioned_ensembl_gene_id":"ENSG00000280438.1","gene_symbol":"AC091932.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8717684,"end":8717883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278877.1","gene_symbol":"AC091932.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8754869,"end":8755159,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244621.1","gene_symbol":"RPS17P11","gene_name":"ribosomal protein S17 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36132]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271072","summary":null,"start":52282567,"end":52282859,"strand":1,"description":"ribosomal protein S17 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:36132]"}, {"versioned_ensembl_gene_id":"ENSG00000272498.1","gene_symbol":"AC090948.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16339308,"end":16339871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250827.1","gene_symbol":"MFSD4BP1","gene_name":"major facilitator superfamily domain containing 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50626]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128154","summary":null,"start":52579555,"end":52581106,"strand":-1,"description":"major facilitator superfamily domain containing 4B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50626]"}, {"versioned_ensembl_gene_id":"ENSG00000260981.1","gene_symbol":"AC091932.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8785042,"end":8785468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000154814.13","gene_symbol":"OXNAD1","gene_name":"oxidoreductase NAD binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25128]","synonyms":"MGC15763","biotype":"protein_coding","ncbi_id":"92106","summary":null,"start":16265160,"end":16350299,"strand":1,"description":"oxidoreductase NAD binding domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25128]"}, {"versioned_ensembl_gene_id":"ENSG00000228875.8","gene_symbol":"CSNK2B","gene_name":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]","synonyms":"Ckb2,Ckb1","biotype":"protein_coding","ncbi_id":"1460","summary":"This gene encodes the beta subunit of casein kinase II, a ubiquitous protein kinase which regulates metabolic pathways, signal transduction, transcription, translation, and replication. The enzyme is composed of three subunits, alpha, alpha prime and beta, which form a tetrameric holoenzyme. The alpha and alpha prime subunits are catalytic, while the beta subunit serves regulatory functions. The enzyme localizes to the endoplasmic reticulum and the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":31652646,"end":31660956,"strand":1,"description":"casein kinase 2 beta [Source:HGNC Symbol;Acc:HGNC:2460]"}, {"versioned_ensembl_gene_id":"ENSG00000260721.1","gene_symbol":"AF067845.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1368642,"end":1369833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134765.9","gene_symbol":"DSC1","gene_name":"desmocollin 1 [Source:HGNC Symbol;Acc:HGNC:3035]","synonyms":"CDHF1","biotype":"protein_coding","ncbi_id":"1823","summary":"The protein encoded by this gene is a calcium-dependent glycoprotein that is a member of the desmocollin subfamily of the cadherin superfamily. These desmosomal family members, along with the desmogleins, are found primarily in epithelial cells where they constitute the adhesive proteins of the desmosome cell-cell junction and are required for cell adhesion and desmosome formation. A subtype of IgA pemphigus, a life-threatening autoimmune disease, is characterized by the presence of autoantibodies that target the encoded protein. The desmosomal family members are arranged in two clusters on chromosome 18. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature protein. [provided by RefSeq, Nov 2015]","start":31129236,"end":31162856,"strand":-1,"description":"desmocollin 1 [Source:HGNC Symbol;Acc:HGNC:3035]"}, {"versioned_ensembl_gene_id":"ENSG00000198010.12","gene_symbol":"DLGAP2","gene_name":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]","synonyms":"ERICH1-AS1,DAP2,DAP-2,C8orf68,SAPAP2,C8orf68,ERICH1-AS1","biotype":"protein_coding","ncbi_id":"9228","summary":"The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]","start":737596,"end":1708474,"strand":1,"description":"DLG associated protein 2 [Source:HGNC Symbol;Acc:HGNC:2906]"}, {"versioned_ensembl_gene_id":"ENSG00000251303.1","gene_symbol":"CAB39P1","gene_name":"calcium binding protein 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51641]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481732","summary":null,"start":60630514,"end":60630973,"strand":1,"description":"calcium binding protein 39 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51641]"}, {"versioned_ensembl_gene_id":"ENSG00000072274.12","gene_symbol":"TFRC","gene_name":"transferrin receptor [Source:HGNC Symbol;Acc:HGNC:11763]","synonyms":"p90,CD71,TFR1","biotype":"protein_coding","ncbi_id":"7037","summary":"This gene encodes a cell surface receptor necessary for cellular iron uptake by the process of receptor-mediated endocytosis. This receptor is required for erythropoiesis and neurologic development. Multiple alternatively spliced variants have been identified. [provided by RefSeq, Sep 2015]","start":196027183,"end":196082189,"strand":-1,"description":"transferrin receptor [Source:HGNC Symbol;Acc:HGNC:11763]"}, {"versioned_ensembl_gene_id":"ENSG00000279519.1","gene_symbol":"AC007382.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36839922,"end":36842539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183087.14","gene_symbol":"GAS6","gene_name":"growth arrest specific 6 [Source:HGNC Symbol;Acc:HGNC:4168]","synonyms":"FLJ34709,DKFZp666G247,AXSF,AXLLG","biotype":"protein_coding","ncbi_id":"2621","summary":"This gene encodes a gamma-carboxyglutamic acid (Gla)-containing protein thought to be involved in the stimulation of cell proliferation. This gene is frequently overexpressed in many cancers and has been implicated as an adverse prognostic marker. Elevated protein levels are additionally associated with a variety of disease states, including venous thromboembolic disease, systemic lupus erythematosus, chronic renal failure, and preeclampsia. [provided by RefSeq, Aug 2014]","start":113820549,"end":113864067,"strand":-1,"description":"growth arrest specific 6 [Source:HGNC Symbol;Acc:HGNC:4168]"}, {"versioned_ensembl_gene_id":"ENSG00000123329.17","gene_symbol":"ARHGAP9","gene_name":"Rho GTPase activating protein 9 [Source:HGNC Symbol;Acc:HGNC:14130]","synonyms":"MGC1295,10C","biotype":"protein_coding","ncbi_id":"64333","summary":"This gene encodes a member of the Rho-GAP family of GTPase activating proteins. The protein has substantial GAP activity towards several Rho-family GTPases in vitro, converting them to an inactive GDP-bound state. It is implicated in regulating adhesion of hematopoietic cells to the extracellular matrix. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":57472255,"end":57488814,"strand":-1,"description":"Rho GTPase activating protein 9 [Source:HGNC Symbol;Acc:HGNC:14130]"}, {"versioned_ensembl_gene_id":"ENSG00000232456.1","gene_symbol":"AL355994.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16035178,"end":16040029,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274776.1","gene_symbol":"AC090241.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46786699,"end":46789297,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272156.1","gene_symbol":"AC008280.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54082554,"end":54085066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235937.1","gene_symbol":"AC008280.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54029552,"end":54030682,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103194.15","gene_symbol":"USP10","gene_name":"ubiquitin specific peptidase 10 [Source:HGNC Symbol;Acc:HGNC:12608]","synonyms":"UBPO,KIAA0190","biotype":"protein_coding","ncbi_id":"9100","summary":"Ubiquitin is a highly conserved protein that is covalently linked to other proteins to regulate their function and degradation. This gene encodes a member of the ubiquitin-specific protease family of cysteine proteases. The enzyme specifically cleaves ubiquitin from ubiquitin-conjugated protein substrates. The protein is found in the nucleus and cytoplasm. It functions as a co-factor of the DNA-bound androgen receptor complex, and is inhibited by a protein in the Ras-GTPase pathway. The human genome contains several pseudogenes similar to this gene. Several transcript variants, some protein-coding and others not protein-coding, have been found for this gene. [provided by RefSeq, Jan 2013]","start":84699978,"end":84779922,"strand":1,"description":"ubiquitin specific peptidase 10 [Source:HGNC Symbol;Acc:HGNC:12608]"}, {"versioned_ensembl_gene_id":"ENSG00000233266.1","gene_symbol":"HMGB1P31","gene_name":"high mobility group box 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39122]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873894","summary":null,"start":54051334,"end":54051760,"strand":1,"description":"high mobility group box 1 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:39122]"}, {"versioned_ensembl_gene_id":"ENSG00000278577.1","gene_symbol":"AC092634.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":63993904,"end":63994006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163075.12","gene_symbol":"CFAP221","gene_name":"cilia and flagella associated protein 221 [Source:HGNC Symbol;Acc:HGNC:33720]","synonyms":"PCDP1,FAP221","biotype":"protein_coding","ncbi_id":"200373","summary":null,"start":119544432,"end":119662251,"strand":1,"description":"cilia and flagella associated protein 221 [Source:HGNC Symbol;Acc:HGNC:33720]"}, {"versioned_ensembl_gene_id":"ENSG00000215403.1","gene_symbol":"LL22NC01-81G9.3","gene_name":"uncharacterized protein FLJ39582-like [Source:NCBI gene;Acc:100506241]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506241","summary":null,"start":36965248,"end":36968172,"strand":1,"description":"uncharacterized protein FLJ39582-like [Source:NCBI gene;Acc:100506241]"}, {"versioned_ensembl_gene_id":"ENSG00000256897.1","gene_symbol":"AC018410.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47220218,"end":47221751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241149.3","gene_symbol":"AC115220.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":63998874,"end":64016130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137824.15","gene_symbol":"RMDN3","gene_name":"regulator of microtubule dynamics 3 [Source:HGNC Symbol;Acc:HGNC:25550]","synonyms":"RMD3,PTPIP51,FLJ10579,FAM82C,FAM82A2","biotype":"protein_coding","ncbi_id":"55177","summary":null,"start":40735884,"end":40755851,"strand":-1,"description":"regulator of microtubule dynamics 3 [Source:HGNC Symbol;Acc:HGNC:25550]"}, {"versioned_ensembl_gene_id":"ENSG00000235522.6","gene_symbol":"AC010978.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":105846534,"end":105857177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232414.6","gene_symbol":"CYP21A2","gene_name":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]","synonyms":"CPS1,CYP21B,CAH1,CYP21,CA21H,P450c21B","biotype":"protein_coding","ncbi_id":"1589","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":32014113,"end":32017485,"strand":1,"description":"cytochrome P450 family 21 subfamily A member 2 [Source:HGNC Symbol;Acc:HGNC:2600]"}, {"versioned_ensembl_gene_id":"ENSG00000104918.7","gene_symbol":"RETN","gene_name":"resistin [Source:HGNC Symbol;Acc:HGNC:20389]","synonyms":"RETN1,FIZZ3,ADSF","biotype":"protein_coding","ncbi_id":"56729","summary":"This gene belongs to the family defined by the mouse resistin-like genes. The characteristic feature of this family is the C-terminal stretch of 10 cys residues with identical spacing. The mouse homolog of this protein is secreted by adipocytes, and may be the hormone potentially linking obesity to type II diabetes. The encoded protein also has an antimicrobial role in skin, displaying antibacterial activity against both Gram positive and Gram negative bacteria. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2020]","start":7669044,"end":7670454,"strand":1,"description":"resistin [Source:HGNC Symbol;Acc:HGNC:20389]"}, {"versioned_ensembl_gene_id":"ENSG00000274311.4","gene_symbol":"LILRB5","gene_name":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]","synonyms":"LIR-8,CD85c,LIR8","biotype":"protein_coding","ncbi_id":"10990","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54251046,"end":54258245,"strand":-1,"description":"leukocyte immunoglobulin like receptor B5 [Source:HGNC Symbol;Acc:HGNC:6609]"}, {"versioned_ensembl_gene_id":"ENSG00000237977.1","gene_symbol":"EIF4HP2","gene_name":"eukaryotic translation initiation factor 4H pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49036]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421545","summary":null,"start":30902219,"end":30902781,"strand":1,"description":"eukaryotic translation initiation factor 4H pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49036]"}, {"versioned_ensembl_gene_id":"ENSG00000233978.1","gene_symbol":"AC016735.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43041193,"end":43043782,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168356.11","gene_symbol":"SCN11A","gene_name":"sodium voltage-gated channel alpha subunit 11 [Source:HGNC Symbol;Acc:HGNC:10583]","synonyms":"SNS-2,SCN12A,Nav1.9,NaN","biotype":"protein_coding","ncbi_id":"11280","summary":"Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is highly expressed in nociceptive neurons of dorsal root ganglia and trigeminal ganglia. It mediates brain-derived neurotrophic factor-evoked membrane depolarization and is a major effector of peripheral inflammatory pain hypersensitivity. Mutations in this gene have been associated with hereditary sensory and autonomic neuropathy type VII and familial episodic pain syndrome-3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2017]","start":38845769,"end":38950561,"strand":-1,"description":"sodium voltage-gated channel alpha subunit 11 [Source:HGNC Symbol;Acc:HGNC:10583]"}, {"versioned_ensembl_gene_id":"ENSG00000281691.1","gene_symbol":"RBM5-AS1","gene_name":"RBM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48871]","synonyms":"LUST","biotype":"antisense_RNA","ncbi_id":"100775107","summary":"This gene produces a non-coding RNA in antisense to the RNA binding motif protein 5 (RBM5) gene. This transcript interacts with beta catenin and may regulate expression of WNT target genes. [provided by RefSeq, Sep 2016]","start":50099603,"end":50100988,"strand":-1,"description":"RBM5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:48871]"}, {"versioned_ensembl_gene_id":"ENSG00000230587.1","gene_symbol":"AC093609.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43097746,"end":43102691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277920.1","gene_symbol":"AC138969.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16351545,"end":16351653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000001617.11","gene_symbol":"SEMA3F","gene_name":"semaphorin 3F [Source:HGNC Symbol;Acc:HGNC:10728]","synonyms":"SEMAK,Sema4","biotype":"protein_coding","ncbi_id":"6405","summary":"This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin loop and a C-terminal basic domain. This gene is expressed by the endothelial cells where it was found to act in an autocrine fashion to induce apoptosis, inhibit cell proliferation and survival, and function as an anti-tumorigenic agent. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":50155045,"end":50189075,"strand":1,"description":"semaphorin 3F [Source:HGNC Symbol;Acc:HGNC:10728]"}, {"versioned_ensembl_gene_id":"ENSG00000234154.10","gene_symbol":"HLA-DMB","gene_name":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]","synonyms":"D6S221E,RING7","biotype":"protein_coding","ncbi_id":"3109","summary":"HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32856943,"end":32875441,"strand":-1,"description":"major histocompatibility complex, class II, DM beta [Source:HGNC Symbol;Acc:HGNC:4935]"}, {"versioned_ensembl_gene_id":"ENSG00000152518.7","gene_symbol":"ZFP36L2","gene_name":"ZFP36 ring finger protein like 2 [Source:HGNC Symbol;Acc:HGNC:1108]","synonyms":"RNF162C,ERF2,BRF2,TIS11D","biotype":"protein_coding","ncbi_id":"678","summary":"This gene is a member of the TIS11 family of early response genes. Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. [provided by RefSeq, Jul 2008]","start":43222402,"end":43226609,"strand":-1,"description":"ZFP36 ring finger protein like 2 [Source:HGNC Symbol;Acc:HGNC:1108]"}, {"versioned_ensembl_gene_id":"ENSG00000156869.12","gene_symbol":"FRRS1","gene_name":"ferric chelate reductase 1 [Source:HGNC Symbol;Acc:HGNC:27622]","synonyms":"SDR2,SDFR2","biotype":"protein_coding","ncbi_id":"391059","summary":"Members of the cytochrome b561 (CYB561; MIM 600019) family, including FRRS1, reduce ferric to ferrous iron before its transport from the endosome to the cytoplasm (Vargas et al., 2003 [PubMed 14499595]).[supplied by OMIM, Mar 2008]","start":99708703,"end":99766631,"strand":-1,"description":"ferric chelate reductase 1 [Source:HGNC Symbol;Acc:HGNC:27622]"}, {"versioned_ensembl_gene_id":"ENSG00000254207.1","gene_symbol":"AC100797.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":725188,"end":725877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213949.8","gene_symbol":"ITGA1","gene_name":"integrin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6134]","synonyms":"VLA1,CD49a","biotype":"protein_coding","ncbi_id":"3672","summary":"This gene encodes the alpha 1 subunit of integrin receptors. This protein heterodimerizes with the beta 1 subunit to form a cell-surface receptor for collagen and laminin. The heterodimeric receptor is involved in cell-cell adhesion and may play a role in inflammation and fibrosis. The alpha 1 subunit contains an inserted (I) von Willebrand factor type I domain which is thought to be involved in collagen binding. [provided by RefSeq, Jul 2008]","start":52787896,"end":52959210,"strand":1,"description":"integrin subunit alpha 1 [Source:HGNC Symbol;Acc:HGNC:6134]"}, {"versioned_ensembl_gene_id":"ENSG00000166598.14","gene_symbol":"HSP90B1","gene_name":"heat shock protein 90 beta family member 1 [Source:HGNC Symbol;Acc:HGNC:12028]","synonyms":"TRA1,GRP94,GP96","biotype":"protein_coding","ncbi_id":"7184","summary":"This gene encodes a member of a family of adenosine triphosphate(ATP)-metabolizing molecular chaperones with roles in stabilizing and folding other proteins. The encoded protein is localized to melanosomes and the endoplasmic reticulum. Expression of this protein is associated with a variety of pathogenic states, including tumor formation. There is a microRNA gene located within the 5' exon of this gene. There are pseudogenes for this gene on chromosomes 1 and 15. [provided by RefSeq, Aug 2012]","start":103930107,"end":103953645,"strand":1,"description":"heat shock protein 90 beta family member 1 [Source:HGNC Symbol;Acc:HGNC:12028]"}, {"versioned_ensembl_gene_id":"ENSG00000124343.12","gene_symbol":"XG","gene_name":"Xg blood group [Source:HGNC Symbol;Acc:HGNC:12806]","synonyms":"PBDX","biotype":"protein_coding","ncbi_id":"7499","summary":"This gene encodes the XG blood group antigen, and is located at the pseudoautosomal boundary on the short (p) arm of chromosome X. The three 5' exons reside in the pseudoautosomal region and the remaining exons within the X-specific end. A truncated copy of this gene is found on the Y chromosome at the pseudoautosomal boundary. It is transcribed, but not expected to make a Y-chromosome specific gene product. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":2752050,"end":2815927,"strand":1,"description":"Xg blood group [Source:HGNC Symbol;Acc:HGNC:12806]"}, {"versioned_ensembl_gene_id":"ENSG00000071051.13","gene_symbol":"NCK2","gene_name":"NCK adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:7665]","synonyms":"NCKbeta","biotype":"protein_coding","ncbi_id":"8440","summary":"This gene encodes a member of the NCK family of adaptor proteins. The protein contains three SH3 domains and one SH2 domain. The protein has no known catalytic function but has been shown to bind and recruit various proteins involved in the regulation of receptor protein tyrosine kinases. It is through these regulatory activities that this protein is believed to be involved in cytoskeletal reorganization. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","start":105744897,"end":105894274,"strand":1,"description":"NCK adaptor protein 2 [Source:HGNC Symbol;Acc:HGNC:7665]"}, {"versioned_ensembl_gene_id":"ENSG00000271620.1","gene_symbol":"IGHV3OR16-7","gene_name":"immunoglobulin heavy variable 3/OR16-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5642]","synonyms":"IGHV3/OR16-7","biotype":"IG_V_pseudogene","ncbi_id":"28309","summary":null,"start":33938337,"end":33938799,"strand":-1,"description":"immunoglobulin heavy variable 3/OR16-7 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5642]"}, {"versioned_ensembl_gene_id":"ENSG00000159445.12","gene_symbol":"THEM4","gene_name":"thioesterase superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:17947]","synonyms":"CTMP","biotype":"protein_coding","ncbi_id":"117145","summary":"Protein kinase B (PKB) is a major downstream target of receptor tyrosine kinases that signal via phosphatidylinositol 3-kinase. Upon cell stimulation, PKB is translocated to the plasma membrane, where it is phosphorylated in the C-terminal regulatory domain. The protein encoded by this gene negatively regulates PKB activity by inhibiting phosphorylation. Transcription of this gene is commonly downregulated in glioblastomas. [provided by RefSeq, Jul 2008]","start":151873584,"end":151909808,"strand":-1,"description":"thioesterase superfamily member 4 [Source:HGNC Symbol;Acc:HGNC:17947]"}, {"versioned_ensembl_gene_id":"ENSG00000279873.2","gene_symbol":"LINC01126","gene_name":"long intergenic non-protein coding RNA 1126 [Source:NCBI gene;Acc:100129726]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100129726","summary":null,"start":43227210,"end":43228855,"strand":1,"description":"long intergenic non-protein coding RNA 1126 [Source:NCBI gene;Acc:100129726]"}, {"versioned_ensembl_gene_id":"ENSG00000184497.12","gene_symbol":"TMEM255B","gene_name":"transmembrane protein 255B [Source:HGNC Symbol;Acc:HGNC:28297]","synonyms":"MGC20579,FAM70B","biotype":"protein_coding","ncbi_id":"348013","summary":null,"start":113759240,"end":113816995,"strand":1,"description":"transmembrane protein 255B [Source:HGNC Symbol;Acc:HGNC:28297]"}, {"versioned_ensembl_gene_id":"ENSG00000117215.14","gene_symbol":"PLA2G2D","gene_name":"phospholipase A2 group IID [Source:HGNC Symbol;Acc:HGNC:9033]","synonyms":"sPLA2S","biotype":"protein_coding","ncbi_id":"26279","summary":"This gene encodes a secreted member of the phospholipase A2 family, and is found in a cluster of related family members on chromosome 1. Phospholipase A2 family members hydrolyze the sn-2 fatty acid ester bond of glycerophospholipids to produce lysophospholipids and free fatty acid. This gene may be involved in inflammation and immune response, and in weight loss associated with chronic obstructive pulmonary disease. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]","start":20111939,"end":20119566,"strand":-1,"description":"phospholipase A2 group IID [Source:HGNC Symbol;Acc:HGNC:9033]"}, {"versioned_ensembl_gene_id":"ENSG00000260493.1","gene_symbol":"AC011773.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85172077,"end":85177062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243164.1","gene_symbol":"AC087879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73648666,"end":73649039,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257750.1","gene_symbol":"LINC02445","gene_name":"long intergenic non-protein coding RNA 2445 [Source:HGNC Symbol;Acc:HGNC:53377]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369840","summary":null,"start":73760689,"end":73798727,"strand":1,"description":"long intergenic non-protein coding RNA 2445 [Source:HGNC Symbol;Acc:HGNC:53377]"}, {"versioned_ensembl_gene_id":"ENSG00000227827.3","gene_symbol":"AC138969.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16356224,"end":16377507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257587.1","gene_symbol":"AC136188.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":73906940,"end":73919337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237181.1","gene_symbol":"AC147651.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":603185,"end":608482,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258332.1","gene_symbol":"LINC02394","gene_name":"long intergenic non-protein coding RNA 2394 [Source:HGNC Symbol;Acc:HGNC:53321]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369841","summary":null,"start":74039086,"end":74045828,"strand":1,"description":"long intergenic non-protein coding RNA 2394 [Source:HGNC Symbol;Acc:HGNC:53321]"}, {"versioned_ensembl_gene_id":"ENSG00000229380.1","gene_symbol":"AC147651.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":561958,"end":565619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231996.1","gene_symbol":"AC096949.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99842610,"end":99842761,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164818.15","gene_symbol":"DNAAF5","gene_name":"dynein axonemal assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:26013]","synonyms":"HEATR2,FLJ39381,FLJ31671,FLJ25564,FLJ20397,CILD18","biotype":"protein_coding","ncbi_id":"54919","summary":"The protein encoded by this gene is essential for the preassembly or stability of axonemal dynein arms, and is found only in organisms with motile cilia and flagella. Mutations in this gene are associated with primary ciliary dyskinesia-18, a disorder characterized by abnormalities of motile cilia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]","start":726701,"end":786475,"strand":1,"description":"dynein axonemal assembly factor 5 [Source:HGNC Symbol;Acc:HGNC:26013]"}, {"versioned_ensembl_gene_id":"ENSG00000131375.9","gene_symbol":"CAPN7","gene_name":"calpain 7 [Source:HGNC Symbol;Acc:HGNC:1484]","synonyms":"PalBH","biotype":"protein_coding","ncbi_id":"23473","summary":"Calpains are ubiquitous, well-conserved family of calcium-dependent, cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large subunit possesses a cysteine protease domain, and both subunits possess calcium-binding domains. Calpains have been implicated in neurodegenerative processes, as their activation can be triggered by calcium influx and oxidative stress. The function of the protein encoded by this gene is not known. An orthologue has been found in mouse but it seems to diverge from other family members. The mouse orthologue is thought to be calcium independent with protease activity. [provided by RefSeq, Jul 2008]","start":15206152,"end":15252918,"strand":1,"description":"calpain 7 [Source:HGNC Symbol;Acc:HGNC:1484]"}, {"versioned_ensembl_gene_id":"ENSG00000251138.6","gene_symbol":"AC090502.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74133166,"end":74402535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234459.1","gene_symbol":"AC002064.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90266034,"end":90270216,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233695.2","gene_symbol":"GAS6-AS1","gene_name":"GAS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39826]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"650669","summary":null,"start":113815630,"end":113845744,"strand":1,"description":"GAS6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39826]"}, {"versioned_ensembl_gene_id":"ENSG00000105792.19","gene_symbol":"CFAP69","gene_name":"cilia and flagella associated protein 69 [Source:HGNC Symbol;Acc:HGNC:26107]","synonyms":"FLJ21062,FAP69,C7orf63","biotype":"protein_coding","ncbi_id":"79846","summary":null,"start":90245174,"end":90311063,"strand":1,"description":"cilia and flagella associated protein 69 [Source:HGNC Symbol;Acc:HGNC:26107]"}, {"versioned_ensembl_gene_id":"ENSG00000257113.1","gene_symbol":"AC090502.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74274952,"end":74275231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213842.2","gene_symbol":"SUGT1P2","gene_name":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31377]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728706","summary":null,"start":32752910,"end":32753901,"strand":1,"description":"SGT1 homolog, MIS12 kinetochore complex assembly cochaperone pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:31377]"}, {"versioned_ensembl_gene_id":"ENSG00000258320.1","gene_symbol":"AC090502.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74170445,"end":74171830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251224.1","gene_symbol":"CNOT10-AS1","gene_name":"CNOT10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41031]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874109","summary":null,"start":32730635,"end":32737454,"strand":-1,"description":"CNOT10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41031]"}, {"versioned_ensembl_gene_id":"ENSG00000257183.1","gene_symbol":"AC090502.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74248637,"end":74283669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182973.18","gene_symbol":"CNOT10","gene_name":"CCR4-NOT transcription complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:23817]","synonyms":"FLJ13165,FLJ12890","biotype":"protein_coding","ncbi_id":"25904","summary":null,"start":32685145,"end":32773875,"strand":1,"description":"CCR4-NOT transcription complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:23817]"}, {"versioned_ensembl_gene_id":"ENSG00000257364.1","gene_symbol":"VENTXP3","gene_name":"VENT homeobox pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30902]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"349814","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":74292324,"end":74293096,"strand":1,"description":"VENT homeobox pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:30902]"}, {"versioned_ensembl_gene_id":"ENSG00000182921.9","gene_symbol":"CCDC75P1","gene_name":"coiled-coil domain containing 75 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42659]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344709","summary":null,"start":73182501,"end":73183291,"strand":-1,"description":"coiled-coil domain containing 75 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42659]"}, {"versioned_ensembl_gene_id":"ENSG00000177606.6","gene_symbol":"JUN","gene_name":"Jun proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6204]","synonyms":"c-Jun,AP-1","biotype":"protein_coding","ncbi_id":"3725","summary":"This gene is the putative transforming gene of avian sarcoma virus 17. It encodes a protein which is highly similar to the viral protein, and which interacts directly with specific target DNA sequences to regulate gene expression. This gene is intronless and is mapped to 1p32-p31, a chromosomal region involved in both translocations and deletions in human malignancies. [provided by RefSeq, Jul 2008]","start":58780788,"end":58784327,"strand":-1,"description":"Jun proto-oncogene, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:6204]"}, {"versioned_ensembl_gene_id":"ENSG00000278490.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724454,"end":54736547,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000075651.15","gene_symbol":"PLD1","gene_name":"phospholipase D1 [Source:HGNC Symbol;Acc:HGNC:9067]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5337","summary":"This gene encodes a phosphatidylcholine-specific phospholipase which catalyzes the hydrolysis of phosphatidylcholine in order to yield phosphatidic acid and choline. The enzyme may play a role in signal transduction and subcellular trafficking. Alternative splicing results in multiple transcript variants with both catalytic and regulatory properties. [provided by RefSeq, Sep 2011]","start":171600405,"end":171810950,"strand":-1,"description":"phospholipase D1 [Source:HGNC Symbol;Acc:HGNC:9067]"}, {"versioned_ensembl_gene_id":"ENSG00000243719.7","gene_symbol":"HLA-DMA","gene_name":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]","synonyms":"D6S222E,RING6","biotype":"protein_coding","ncbi_id":"3108","summary":"HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":32870929,"end":32893044,"strand":-1,"description":"major histocompatibility complex, class II, DM alpha [Source:HGNC Symbol;Acc:HGNC:4934]"}, {"versioned_ensembl_gene_id":"ENSG00000234807.5","gene_symbol":"LINC01135","gene_name":"long intergenic non-protein coding RNA 1135 [Source:HGNC Symbol;Acc:HGNC:49450]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100131060","summary":null,"start":58785160,"end":58899594,"strand":1,"description":"long intergenic non-protein coding RNA 1135 [Source:HGNC Symbol;Acc:HGNC:49450]"}, {"versioned_ensembl_gene_id":"ENSG00000163053.10","gene_symbol":"SLC16A14","gene_name":"solute carrier family 16 member 14 [Source:HGNC Symbol;Acc:HGNC:26417]","synonyms":"MCT14,FLJ30794","biotype":"protein_coding","ncbi_id":"151473","summary":null,"start":230034974,"end":230068999,"strand":-1,"description":"solute carrier family 16 member 14 [Source:HGNC Symbol;Acc:HGNC:26417]"}, {"versioned_ensembl_gene_id":"ENSG00000272226.1","gene_symbol":"AL136985.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58812808,"end":58813342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232453.6","gene_symbol":"AC105277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58882868,"end":58903747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159873.9","gene_symbol":"CCDC117","gene_name":"coiled-coil domain containing 117 [Source:HGNC Symbol;Acc:HGNC:26599]","synonyms":"FLJ33814","biotype":"protein_coding","ncbi_id":"150275","summary":null,"start":28772674,"end":28789301,"strand":1,"description":"coiled-coil domain containing 117 [Source:HGNC Symbol;Acc:HGNC:26599]"}, {"versioned_ensembl_gene_id":"ENSG00000231740.1","gene_symbol":"AL136985.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58838448,"end":58851254,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278962.1","gene_symbol":"AC092645.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":112188364,"end":112190635,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230014.1","gene_symbol":"LINC00709","gene_name":"long intergenic non-protein coding RNA 709 [Source:HGNC Symbol;Acc:HGNC:44700]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507163","summary":null,"start":9275833,"end":9287057,"strand":1,"description":"long intergenic non-protein coding RNA 709 [Source:HGNC Symbol;Acc:HGNC:44700]"}, {"versioned_ensembl_gene_id":"ENSG00000235838.1","gene_symbol":"HSP90AB7P","gene_name":"heat shock protein 90 alpha family class B member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44701]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644495","summary":null,"start":9721963,"end":9724416,"strand":-1,"description":"heat shock protein 90 alpha family class B member 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:44701]"}, {"versioned_ensembl_gene_id":"ENSG00000228636.1","gene_symbol":"AL157401.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9758783,"end":9759237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144161.12","gene_symbol":"ZC3H8","gene_name":"zinc finger CCCH-type containing 8 [Source:HGNC Symbol;Acc:HGNC:30941]","synonyms":"ZC3HDC8,Fliz1","biotype":"protein_coding","ncbi_id":"84524","summary":null,"start":112211525,"end":112255136,"strand":-1,"description":"zinc finger CCCH-type containing 8 [Source:HGNC Symbol;Acc:HGNC:30941]"}, {"versioned_ensembl_gene_id":"ENSG00000224788.1","gene_symbol":"AL138775.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10058722,"end":10063502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270739.1","gene_symbol":"AC090953.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16275060,"end":16276632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271964.1","gene_symbol":"AC090948.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16314439,"end":16314987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166869.2","gene_symbol":"CHP2","gene_name":"calcineurin like EF-hand protein 2 [Source:HGNC Symbol;Acc:HGNC:24927]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63928","summary":"This gene product is a small calcium-binding protein that regulates cell pH by controlling plasma membrane-type Na+/H+ exchange activity. This protein shares sequence similarity with calcineurin B and can bind to and stimulate the protein phosphatase activity of calcineurin A (CnA) and functions in the calcineurin/NFAT (nuclear factor of activated T cells) signaling pathway. Another member of the CHP subfamily, Calcineurin B homologous protein 1, is located on Chromosome 15 and is an inhibitor of calcineurin activity and has a genetic phenotype associated with Parkinson's Disease (OMIM:606988). This gene was initially identified as a tumor-associated antigen and was previously referred to as Hepatocellular carcinoma-associated antigen 520. [provided by RefSeq, Jul 2013]","start":23754627,"end":23758951,"strand":1,"description":"calcineurin like EF-hand protein 2 [Source:HGNC Symbol;Acc:HGNC:24927]"}, {"versioned_ensembl_gene_id":"ENSG00000279200.1","gene_symbol":"AC020558.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17616043,"end":17617745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188191.14","gene_symbol":"PRKAR1B","gene_name":"protein kinase cAMP-dependent type I regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9390]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5575","summary":"The protein encoded by this gene is a regulatory subunit of cyclic AMP-dependent protein kinase A (PKA), which is involved in the signaling pathway of the second messenger cAMP. Two regulatory and two catalytic subunits form the PKA holoenzyme, disbands after cAMP binding. The holoenzyme is involved in many cellular events, including ion transport, metabolism, and transcription. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2015]","start":549197,"end":727650,"strand":-1,"description":"protein kinase cAMP-dependent type I regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9390]"}, {"versioned_ensembl_gene_id":"ENSG00000096395.10","gene_symbol":"MLN","gene_name":"motilin [Source:HGNC Symbol;Acc:HGNC:7141]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4295","summary":"This gene encodes a small peptide hormone that is secreted by cells of the small intestine to regulate gastrointestinal contractions and motility. Proteolytic processing of the secreted protein produces the mature peptide and a byproduct referred to as motilin-associated peptide (MAP). Three transcript variants encoding different preproprotein isoforms but the same mature peptide have been found for this gene. [provided by RefSeq, May 2010]","start":33794673,"end":33804011,"strand":-1,"description":"motilin [Source:HGNC Symbol;Acc:HGNC:7141]"}, {"versioned_ensembl_gene_id":"ENSG00000173535.13","gene_symbol":"TNFRSF10C","gene_name":"TNF receptor superfamily member 10c [Source:HGNC Symbol;Acc:HGNC:11906]","synonyms":"TRID,TRAILR3,LIT,DcR1,CD263","biotype":"protein_coding","ncbi_id":"8794","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008]","start":23084355,"end":23117437,"strand":1,"description":"TNF receptor superfamily member 10c [Source:HGNC Symbol;Acc:HGNC:11906]"}, {"versioned_ensembl_gene_id":"ENSG00000152620.12","gene_symbol":"NADK2","gene_name":"NAD kinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26404]","synonyms":"NADKD1,MNADK,FLJ30596,C5orf33","biotype":"protein_coding","ncbi_id":"133686","summary":"This gene encodes a mitochondrial kinase that catalyzes the phosphorylation of NAD to yield NADP. Mutations in this gene result in 2,4-dienoyl-CoA reductase deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":36192592,"end":36242279,"strand":-1,"description":"NAD kinase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:26404]"}, {"versioned_ensembl_gene_id":"ENSG00000234936.1","gene_symbol":"AC010883.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43229573,"end":43233394,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115970.18","gene_symbol":"THADA","gene_name":"THADA, armadillo repeat containing [Source:HGNC Symbol;Acc:HGNC:19217]","synonyms":"KIAA1767,GITA,FLJ21877,ARMC13","biotype":"protein_coding","ncbi_id":"63892","summary":"This gene is the target of 2p21 choromosomal aberrations in benign thyroid adenomas. Single nucleotide polymorphisms (SNPs) in this gene may be associated with type 2 diabetes and polycystic ovary syndrome. The encoded protein is likely involved in the death receptor pathway and apoptosis. [provided by RefSeq, Sep 2016]","start":43230836,"end":43596046,"strand":-1,"description":"THADA, armadillo repeat containing [Source:HGNC Symbol;Acc:HGNC:19217]"}, {"versioned_ensembl_gene_id":"ENSG00000279756.1","gene_symbol":"AC012317.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23753689,"end":23755939,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000071073.12","gene_symbol":"MGAT4A","gene_name":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A [Source:HGNC Symbol;Acc:HGNC:7047]","synonyms":"GnT-Iva,GnT-4a","biotype":"protein_coding","ncbi_id":"11320","summary":"This gene encodes a key glycosyltransferase that regulates the formation of tri- and multiantennary branching structures in the Golgi apparatus. The encoded protein, in addition to the related isoenzyme B, catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc in a beta-1,4 linkage to the Man-alpha-1,3-Man-beta-1,4-GlcNAc arm of R-Man-alpha-1,6(GlcNAc-beta-1,2-Man-alpha-1,3)Man-beta-1,4-GlcNAc-beta-1,4-GlcNAc-beta-1-Asn. The encoded protein may play a role in regulating the availability of serum glycoproteins, oncogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":98619106,"end":98731126,"strand":-1,"description":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A [Source:HGNC Symbol;Acc:HGNC:7047]"}, {"versioned_ensembl_gene_id":"ENSG00000261820.1","gene_symbol":"DNM1P49","gene_name":"dynamin 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:47040]","synonyms":"DNM1DN8@","biotype":"unprocessed_pseudogene","ncbi_id":"730058","summary":null,"start":75791470,"end":75792683,"strand":-1,"description":"dynamin 1 pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:47040]"}, {"versioned_ensembl_gene_id":"ENSG00000229919.3","gene_symbol":"ELOCP3","gene_name":"elongin C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29457]","synonyms":"TCEB1P3,dJ254P11.1","biotype":"processed_pseudogene","ncbi_id":"644540","summary":null,"start":10174230,"end":10174577,"strand":1,"description":"elongin C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29457]"}, {"versioned_ensembl_gene_id":"ENSG00000272436.1","gene_symbol":"CUX2P1","gene_name":"cut like homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33694]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100126596","summary":null,"start":10257169,"end":10257466,"strand":-1,"description":"cut like homeobox 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33694]"}, {"versioned_ensembl_gene_id":"ENSG00000234306.1","gene_symbol":"AL583859.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10365180,"end":10366487,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229324.1","gene_symbol":"NUTF2P7","gene_name":"nuclear transport factor 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50458]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287868","summary":null,"start":71016531,"end":71016905,"strand":-1,"description":"nuclear transport factor 2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:50458]"}, {"versioned_ensembl_gene_id":"ENSG00000227536.1","gene_symbol":"SOCS5P4","gene_name":"suppressor of cytokine signaling 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44600]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132415","summary":null,"start":71043214,"end":71045470,"strand":-1,"description":"suppressor of cytokine signaling 5 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:44600]"}, {"versioned_ensembl_gene_id":"ENSG00000279098.1","gene_symbol":"AC097460.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":99942081,"end":99942522,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164031.16","gene_symbol":"DNAJB14","gene_name":"DnaJ heat shock protein family (Hsp40) member B14 [Source:HGNC Symbol;Acc:HGNC:25881]","synonyms":"FLJ14281","biotype":"protein_coding","ncbi_id":"79982","summary":null,"start":99896248,"end":99946726,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member B14 [Source:HGNC Symbol;Acc:HGNC:25881]"}, {"versioned_ensembl_gene_id":"ENSG00000090020.10","gene_symbol":"SLC9A1","gene_name":"solute carrier family 9 member A1 [Source:HGNC Symbol;Acc:HGNC:11071]","synonyms":"PPP1R143,NHE1,APNH","biotype":"protein_coding","ncbi_id":"6548","summary":"This gene encodes a Na+/H+ antiporter that is a member of the solute carrier family 9. The encoded protein is a plasma membrane transporter that is expressed in the kidney and intestine. This protein plays a central role in regulating pH homeostasis, cell migration and cell volume. This protein may also be involved in tumor growth. [provided by RefSeq, Sep 2011]","start":27098815,"end":27166981,"strand":-1,"description":"solute carrier family 9 member A1 [Source:HGNC Symbol;Acc:HGNC:11071]"}, {"versioned_ensembl_gene_id":"ENSG00000100983.9","gene_symbol":"GSS","gene_name":"glutathione synthetase [Source:HGNC Symbol;Acc:HGNC:4624]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2937","summary":"Glutathione is important for a variety of biological functions, including protection of cells from oxidative damage by free radicals, detoxification of xenobiotics, and membrane transport. The protein encoded by this gene functions as a homodimer to catalyze the second step of glutathione biosynthesis, which is the ATP-dependent conversion of gamma-L-glutamyl-L-cysteine to glutathione. Defects in this gene are a cause of glutathione synthetase deficiency. [provided by RefSeq, Jul 2008]","start":34928430,"end":34955817,"strand":-1,"description":"glutathione synthetase [Source:HGNC Symbol;Acc:HGNC:4624]"}, {"versioned_ensembl_gene_id":"ENSG00000184908.17","gene_symbol":"CLCNKB","gene_name":"chloride voltage-gated channel Kb [Source:HGNC Symbol;Acc:HGNC:2027]","synonyms":"hClC-Kb","biotype":"protein_coding","ncbi_id":"1188","summary":"The protein encoded by this gene is a member of the family of voltage-gated chloride channels. Chloride channels have several functions, including the regulation of cell volume, membrane potential stabilization, signal transduction and transepithelial transport. This gene is expressed predominantly in the kidney and may be important for renal salt reabsorption. Mutations in this gene are associated with autosomal recessive Bartter syndrome type 3 (BS3). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":16043736,"end":16057308,"strand":1,"description":"chloride voltage-gated channel Kb [Source:HGNC Symbol;Acc:HGNC:2027]"}, {"versioned_ensembl_gene_id":"ENSG00000278934.1","gene_symbol":"AC117489.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":73624410,"end":73627626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234673.1","gene_symbol":"AL662845.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32892631,"end":32893145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188817.7","gene_symbol":"SNTN","gene_name":"sentan, cilia apical structure protein [Source:HGNC Symbol;Acc:HGNC:33706]","synonyms":"S100AL,FLJ44379","biotype":"protein_coding","ncbi_id":"132203","summary":null,"start":63652668,"end":63679020,"strand":1,"description":"sentan, cilia apical structure protein [Source:HGNC Symbol;Acc:HGNC:33706]"}, {"versioned_ensembl_gene_id":"ENSG00000121440.14","gene_symbol":"PDZRN3","gene_name":"PDZ domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:17704]","synonyms":"SEMACAP3,LNX3,KIAA1095","biotype":"protein_coding","ncbi_id":"23024","summary":"This gene encodes a member of the LNX (Ligand of Numb Protein-X) family of RING-type ubiquitin E3 ligases. This protein may function in vascular morphogenesis and the differentiation of adipocytes, osteoblasts and myoblasts. This protein may be targeted for degradation by the human papilloma virus E6 protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":73382433,"end":73624940,"strand":-1,"description":"PDZ domain containing ring finger 3 [Source:HGNC Symbol;Acc:HGNC:17704]"}, {"versioned_ensembl_gene_id":"ENSG00000106100.10","gene_symbol":"NOD1","gene_name":"nucleotide binding oligomerization domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16390]","synonyms":"NLRC1,CLR7.1,CARD4","biotype":"protein_coding","ncbi_id":"10392","summary":"This gene encodes a member of the nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family of proteins. The encoded protein plays a role in innate immunity by acting as a pattern-recognition receptor (PRR) that binds bacterial peptidoglycans and initiates inflammation. This protein has also been implicated in the immune response to viral and parasitic infection. Major structural features of this protein include an N-terminal caspase recruitment domain (CARD), a centrally located nucleotide-binding domain (NBD), and 10 tandem leucine-rich repeats (LRRs) in its C terminus. The CARD is involved in apoptotic signaling, LRRs participate in protein-protein interactions, and mutations in the NBD may affect the process of oligomerization and subsequent function of the LRR domain. Mutations in this gene are associated with asthma, inflammatory bowel disease, Behcet disease and sarcoidosis in human patients. [provided by RefSeq, Aug 2017]","start":30424527,"end":30478784,"strand":-1,"description":"nucleotide binding oligomerization domain containing 1 [Source:HGNC Symbol;Acc:HGNC:16390]"}, {"versioned_ensembl_gene_id":"ENSG00000253621.1","gene_symbol":"RPSAP74","gene_name":"ribosomal protein SA pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:51928]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075113","summary":null,"start":89243401,"end":89243793,"strand":-1,"description":"ribosomal protein SA pseudogene 74 [Source:HGNC Symbol;Acc:HGNC:51928]"}, {"versioned_ensembl_gene_id":"ENSG00000257327.1","gene_symbol":"AC012555.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103841451,"end":103844664,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241809.1","gene_symbol":"AC022133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52903908,"end":52904478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215784.5","gene_symbol":"FAM72D","gene_name":"family with sequence similarity 72 member D [Source:HGNC Symbol;Acc:HGNC:33593]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728833","summary":null,"start":145096000,"end":145112696,"strand":1,"description":"family with sequence similarity 72 member D [Source:HGNC Symbol;Acc:HGNC:33593]"}, {"versioned_ensembl_gene_id":"ENSG00000164171.10","gene_symbol":"ITGA2","gene_name":"integrin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6137]","synonyms":"CD49B","biotype":"protein_coding","ncbi_id":"3673","summary":"This gene encodes the alpha subunit of a transmembrane receptor for collagens and related proteins. The encoded protein forms a heterodimer with a beta subunit and mediates the adhesion of platelets and other cell types to the extracellular matrix. Loss of the encoded protein is associated with bleeding disorder platelet-type 9. Antibodies against this protein are found in several immune disorders, including neonatal alloimmune thrombocytopenia. This gene is located adjacent to a related alpha subunit gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]","start":52989326,"end":53094779,"strand":1,"description":"integrin subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:6137]"}, {"versioned_ensembl_gene_id":"ENSG00000197150.12","gene_symbol":"ABCB8","gene_name":"ATP binding cassette subfamily B member 8 [Source:HGNC Symbol;Acc:HGNC:49]","synonyms":"MABC1,M-ABC1,EST328128","biotype":"protein_coding","ncbi_id":"11194","summary":"This nuclear gene encodes a multi-pass membrane protein that is targeted to the mitochondrial inner membrane. The encoded protein is an ATP-dependent transporter that may mediate the passage of organic and inorganic molecules out of the mitochondria. Loss of function of the related gene in mouse results in a disruption of iron homeostasis between the mitochondria and cytosol. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":151028422,"end":151047782,"strand":1,"description":"ATP binding cassette subfamily B member 8 [Source:HGNC Symbol;Acc:HGNC:49]"}, {"versioned_ensembl_gene_id":"ENSG00000279927.1","gene_symbol":"Z95114.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36066533,"end":36070110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279217.1","gene_symbol":"Z95114.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36071000,"end":36085573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279714.1","gene_symbol":"Z95114.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36091148,"end":36093352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149823.8","gene_symbol":"VPS51","gene_name":"VPS51, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:1172]","synonyms":"FFR,C11orf3,C11orf2,ANG3,ANG2","biotype":"protein_coding","ncbi_id":"738","summary":"This gene encodes a member of the vacuolar protein sorting-associated protein 51 family. The encoded protein is a component of the Golgi-associated retrograde protein complex which acts as a tethering factor for carriers in retrograde transport from the early and late endosomes to the trans-Golgi network. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":65089324,"end":65111860,"strand":1,"description":"VPS51, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:1172]"}, {"versioned_ensembl_gene_id":"ENSG00000253943.1","gene_symbol":"KRT18P37","gene_name":"keratin 18 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:33406]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392214","summary":null,"start":41511240,"end":41512521,"strand":1,"description":"keratin 18 pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:33406]"}, {"versioned_ensembl_gene_id":"ENSG00000279805.1","gene_symbol":"Z95114.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36137430,"end":36139350,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000116095.10","gene_symbol":"PLEKHA3","gene_name":"pleckstrin homology domain containing A3 [Source:HGNC Symbol;Acc:HGNC:14338]","synonyms":"FAPP1","biotype":"protein_coding","ncbi_id":"65977","summary":null,"start":178480468,"end":178516462,"strand":1,"description":"pleckstrin homology domain containing A3 [Source:HGNC Symbol;Acc:HGNC:14338]"}, {"versioned_ensembl_gene_id":"ENSG00000057757.9","gene_symbol":"PITHD1","gene_name":"PITH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25022]","synonyms":"TXNL1CL,HT014,C1orf128","biotype":"protein_coding","ncbi_id":"57095","summary":null,"start":23778405,"end":23788232,"strand":1,"description":"PITH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25022]"}, {"versioned_ensembl_gene_id":"ENSG00000186416.13","gene_symbol":"NKRF","gene_name":"NFKB repressing factor [Source:HGNC Symbol;Acc:HGNC:19374]","synonyms":"NRF,ITBA4","biotype":"protein_coding","ncbi_id":"55922","summary":"This gene encodes a transcriptional repressor that interacts with specific negative regulatory elements to mediate transcriptional repression of certain nuclear factor kappa B responsive genes. The protein localizes predominantly to the nucleolus with a small fraction found in the nucleoplasm and cytoplasm. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":119588337,"end":119605895,"strand":-1,"description":"NFKB repressing factor [Source:HGNC Symbol;Acc:HGNC:19374]"}, {"versioned_ensembl_gene_id":"ENSG00000239215.1","gene_symbol":"AC117503.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":123721246,"end":123721639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185344.13","gene_symbol":"ATP6V0A2","gene_name":"ATPase H+ transporting V0 subunit a2 [Source:HGNC Symbol;Acc:HGNC:18481]","synonyms":"TJ6s,TJ6M,TJ6,Stv1,J6B7,ATP6N1D,ATP6a2,a2,Vph1","biotype":"protein_coding","ncbi_id":"23545","summary":"The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009]","start":123712318,"end":123761755,"strand":1,"description":"ATPase H+ transporting V0 subunit a2 [Source:HGNC Symbol;Acc:HGNC:18481]"}, {"versioned_ensembl_gene_id":"ENSG00000257966.1","gene_symbol":"OLA1P3","gene_name":"Obg-like ATPase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45278]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101060020","summary":null,"start":55870048,"end":55872602,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45278]"}, {"versioned_ensembl_gene_id":"ENSG00000228413.1","gene_symbol":"AC024937.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":196044695,"end":196045254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280185.1","gene_symbol":"AC091932.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8793875,"end":8794197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283752.1","gene_symbol":"AC241585.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":145139986,"end":145148375,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244371.2","gene_symbol":"PFN1P8","gene_name":"profilin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42986]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873744","summary":null,"start":146957117,"end":146957659,"strand":-1,"description":"profilin 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42986]"}, {"versioned_ensembl_gene_id":"ENSG00000270318.1","gene_symbol":"IGHV3OR16-11","gene_name":"immunoglobulin heavy variable 3/OR16-11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5635]","synonyms":"IGHV3/OR16-11","biotype":"IG_V_pseudogene","ncbi_id":"28305","summary":null,"start":33858896,"end":33859352,"strand":-1,"description":"immunoglobulin heavy variable 3/OR16-11 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5635]"}, {"versioned_ensembl_gene_id":"ENSG00000225383.7","gene_symbol":"SFTA1P","gene_name":"surfactant associated 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18383]","synonyms":"SFTPF","biotype":"lincRNA","ncbi_id":"207107","summary":null,"start":10784437,"end":10794980,"strand":-1,"description":"surfactant associated 1, pseudogene [Source:HGNC Symbol;Acc:HGNC:18383]"}, {"versioned_ensembl_gene_id":"ENSG00000104969.9","gene_symbol":"SGTA","gene_name":"small glutamine rich tetratricopeptide repeat containing alpha [Source:HGNC Symbol;Acc:HGNC:10819]","synonyms":"SGT","biotype":"protein_coding","ncbi_id":"6449","summary":"This gene encodes a protein which is capable of interacting with the major nonstructural protein of parvovirus H-1 and 70-kDa heat shock cognate protein; however, its function is not known. Since this transcript is expressed ubiquitously in various tissues, this protein may serve a housekeeping function. [provided by RefSeq, Jul 2008]","start":2754714,"end":2783371,"strand":-1,"description":"small glutamine rich tetratricopeptide repeat containing alpha [Source:HGNC Symbol;Acc:HGNC:10819]"}, {"versioned_ensembl_gene_id":"ENSG00000234336.6","gene_symbol":"JAZF1-AS1","gene_name":"JAZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41218]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100128081","summary":null,"start":28180322,"end":28243917,"strand":1,"description":"JAZF1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41218]"}, {"versioned_ensembl_gene_id":"ENSG00000249375.7","gene_symbol":"CASC11","gene_name":"cancer susceptibility 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48939]","synonyms":"TCONS_00014535,LINC00990,ENST00000518376,CARLo-7","biotype":"lincRNA","ncbi_id":"100270680","summary":null,"start":127686343,"end":127733967,"strand":-1,"description":"cancer susceptibility 11 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:48939]"}, {"versioned_ensembl_gene_id":"ENSG00000091622.15","gene_symbol":"PITPNM3","gene_name":"PITPNM family member 3 [Source:HGNC Symbol;Acc:HGNC:21043]","synonyms":"RDGBA3,NIR1,CORD5,ACKR6","biotype":"protein_coding","ncbi_id":"83394","summary":"This gene encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. The calcium-binding protein has phosphatidylinositol (PI) transfer activity and interacts with the protein tyrosine kinase PTK2B (also known as PYK2). The protein is homologous to a Drosophila protein that is implicated in the visual transduction pathway in flies. Mutations in this gene result in autosomal dominant cone dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]","start":6451264,"end":6556494,"strand":-1,"description":"PITPNM family member 3 [Source:HGNC Symbol;Acc:HGNC:21043]"}, {"versioned_ensembl_gene_id":"ENSG00000158669.11","gene_symbol":"GPAT4","gene_name":"glycerol-3-phosphate acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:20880]","synonyms":"TSARG7,LPAAT-zeta,DKFZp586M1819,AGPAT6","biotype":"protein_coding","ncbi_id":"137964","summary":"Lysophosphatidic acid acyltransferases (EC 2.3.1.51) catalyze the conversion of lysophosphatidic acid (LPA) to phosphatidic acid (PA). LPA and PA are involved in signal transduction and lipid biosynthesis.[supplied by OMIM, Apr 2004]","start":41577187,"end":41625001,"strand":1,"description":"glycerol-3-phosphate acyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:20880]"}, {"versioned_ensembl_gene_id":"ENSG00000106052.13","gene_symbol":"TAX1BP1","gene_name":"Tax1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11575]","synonyms":"TXBP151,CALCOCO3","biotype":"protein_coding","ncbi_id":"8887","summary":"This gene encodes a HTLV-1 tax1 binding protein. The encoded protein interacts with TNFAIP3, and inhibits TNF-induced apoptosis by mediating the TNFAIP3 anti-apoptotic activity. Degradation of this protein by caspase-3-like family proteins is associated with apoptosis induced by TNF. This protein may also have a role in the inhibition of inflammatory signaling pathways. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]","start":27739331,"end":27844564,"strand":1,"description":"Tax1 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:11575]"}, {"versioned_ensembl_gene_id":"ENSG00000228564.1","gene_symbol":"LINC01005","gene_name":"long intergenic non-protein coding RNA 1005 [Source:HGNC Symbol;Acc:HGNC:48963]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506050","summary":null,"start":64027852,"end":64030105,"strand":-1,"description":"long intergenic non-protein coding RNA 1005 [Source:HGNC Symbol;Acc:HGNC:48963]"}, {"versioned_ensembl_gene_id":"ENSG00000236564.1","gene_symbol":"YWHAQP5","gene_name":"YWHAQ pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130391","summary":null,"start":98694109,"end":98695490,"strand":1,"description":"YWHAQ pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37684]"}, {"versioned_ensembl_gene_id":"ENSG00000116544.11","gene_symbol":"DLGAP3","gene_name":"DLG associated protein 3 [Source:HGNC Symbol;Acc:HGNC:30368]","synonyms":"SAPAP3,DAP3","biotype":"protein_coding","ncbi_id":"58512","summary":null,"start":34865436,"end":34929585,"strand":-1,"description":"DLG associated protein 3 [Source:HGNC Symbol;Acc:HGNC:30368]"}, {"versioned_ensembl_gene_id":"ENSG00000214652.5","gene_symbol":"ZNF727","gene_name":"zinc finger protein 727 [Source:HGNC Symbol;Acc:HGNC:22785]","synonyms":"ZNF727P","biotype":"protein_coding","ncbi_id":"442319","summary":null,"start":64045443,"end":64078549,"strand":1,"description":"zinc finger protein 727 [Source:HGNC Symbol;Acc:HGNC:22785]"}, {"versioned_ensembl_gene_id":"ENSG00000257569.1","gene_symbol":"GSTP1P1","gene_name":"glutathione S-transferase pi 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4640]","synonyms":"GSTPP,GSTPL,GSTP1P,GST3L","biotype":"processed_pseudogene","ncbi_id":"2951","summary":null,"start":55900300,"end":55900618,"strand":1,"description":"glutathione S-transferase pi 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4640]"}, {"versioned_ensembl_gene_id":"ENSG00000077721.15","gene_symbol":"UBE2A","gene_name":"ubiquitin conjugating enzyme E2 A [Source:HGNC Symbol;Acc:HGNC:12472]","synonyms":"UBC2,RAD6A,HHR6A","biotype":"protein_coding","ncbi_id":"7319","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, ubiquitin-conjugating enzymes, and ubiquitin-protein ligases. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is required for post-replicative DNA damage repair, and may play a role in transcriptional regulation. Mutations in this gene are associated with cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":119574467,"end":119591083,"strand":1,"description":"ubiquitin conjugating enzyme E2 A [Source:HGNC Symbol;Acc:HGNC:12472]"}, {"versioned_ensembl_gene_id":"ENSG00000153234.13","gene_symbol":"NR4A2","gene_name":"nuclear receptor subfamily 4 group A member 2 [Source:HGNC Symbol;Acc:HGNC:7981]","synonyms":"TINUR,RNR1,NURR1,NOT,HZF-3","biotype":"protein_coding","ncbi_id":"4929","summary":"This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcription factor. Mutations in this gene have been associated with disorders related to dopaminergic dysfunction, including Parkinson disease, schizophernia, and manic depression. Misregulation of this gene may be associated with rheumatoid arthritis. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":156324432,"end":156342348,"strand":-1,"description":"nuclear receptor subfamily 4 group A member 2 [Source:HGNC Symbol;Acc:HGNC:7981]"}, {"versioned_ensembl_gene_id":"ENSG00000279575.1","gene_symbol":"AL583859.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":10394670,"end":10395737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185264.11","gene_symbol":"TEX33","gene_name":"testis expressed 33 [Source:HGNC Symbol;Acc:HGNC:28568]","synonyms":"MGC35206,EAN57,C22orf33","biotype":"protein_coding","ncbi_id":"339669","summary":null,"start":36991120,"end":37007841,"strand":-1,"description":"testis expressed 33 [Source:HGNC Symbol;Acc:HGNC:28568]"}, {"versioned_ensembl_gene_id":"ENSG00000261607.1","gene_symbol":"AC140658.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33948278,"end":33948548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260525.1","gene_symbol":"AC140658.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33875039,"end":33875468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272638.1","gene_symbol":"AC006027.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30424672,"end":30425412,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120647.9","gene_symbol":"CCDC77","gene_name":"coiled-coil domain containing 77 [Source:HGNC Symbol;Acc:HGNC:28203]","synonyms":"MGC13183","biotype":"protein_coding","ncbi_id":"84318","summary":null,"start":389273,"end":442645,"strand":1,"description":"coiled-coil domain containing 77 [Source:HGNC Symbol;Acc:HGNC:28203]"}, {"versioned_ensembl_gene_id":"ENSG00000270111.2","gene_symbol":"AL583859.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10418739,"end":10462349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182858.13","gene_symbol":"ALG12","gene_name":"ALG12, alpha-1,6-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:19358]","synonyms":"CDG1G,ECM39","biotype":"protein_coding","ncbi_id":"79087","summary":"This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]","start":49900229,"end":49918458,"strand":-1,"description":"ALG12, alpha-1,6-mannosyltransferase [Source:HGNC Symbol;Acc:HGNC:19358]"}, {"versioned_ensembl_gene_id":"ENSG00000270401.1","gene_symbol":"AC140658.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33965655,"end":33966091,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228997.1","gene_symbol":"AL136452.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":10776223,"end":10776661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173530.5","gene_symbol":"TNFRSF10D","gene_name":"TNF receptor superfamily member 10d [Source:HGNC Symbol;Acc:HGNC:11907]","synonyms":"TRUNDD,TRAILR4,DcR2,CD264","biotype":"protein_coding","ncbi_id":"8793","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain, a transmembrane domain, and a truncated cytoplamic death domain. This receptor does not induce apoptosis, and has been shown to play an inhibitory role in TRAIL-induced cell apoptosis. [provided by RefSeq, Jul 2008]","start":23135588,"end":23164030,"strand":-1,"description":"TNF receptor superfamily member 10d [Source:HGNC Symbol;Acc:HGNC:11907]"}, {"versioned_ensembl_gene_id":"ENSG00000259842.2","gene_symbol":"IGHV3OR16-16","gene_name":"immunoglobulin heavy variable 3/OR16-16 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5640]","synonyms":"IGHV3/OR16-16","biotype":"unprocessed_pseudogene","ncbi_id":"28300","summary":null,"start":33949976,"end":33950420,"strand":-1,"description":"immunoglobulin heavy variable 3/OR16-16 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5640]"}, {"versioned_ensembl_gene_id":"ENSG00000235016.1","gene_symbol":"SEMA3F-AS1","gene_name":"SEMA3F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40518]","synonyms":"RBM5-AS1","biotype":"antisense_RNA","ncbi_id":"100129060","summary":null,"start":50116022,"end":50156085,"strand":-1,"description":"SEMA3F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40518]"}, {"versioned_ensembl_gene_id":"ENSG00000260781.1","gene_symbol":"ARHGAP23P1","gene_name":"Rho GTPase activating protein 23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45039]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"102577425","summary":null,"start":33907419,"end":33937167,"strand":-1,"description":"Rho GTPase activating protein 23 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45039]"}, {"versioned_ensembl_gene_id":"ENSG00000004534.14","gene_symbol":"RBM6","gene_name":"RNA binding motif protein 6 [Source:HGNC Symbol;Acc:HGNC:9903]","synonyms":"NY-LU-12,g16,DEF3,DEF-3,3G2","biotype":"protein_coding","ncbi_id":"10180","summary":null,"start":49940007,"end":50100045,"strand":1,"description":"RNA binding motif protein 6 [Source:HGNC Symbol;Acc:HGNC:9903]"}, {"versioned_ensembl_gene_id":"ENSG00000280394.1","gene_symbol":"AC011471.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":6263068,"end":6263469,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077935.16","gene_symbol":"SMC1B","gene_name":"structural maintenance of chromosomes 1B [Source:HGNC Symbol;Acc:HGNC:11112]","synonyms":"SMC1L2,bK268H5","biotype":"protein_coding","ncbi_id":"27127","summary":"SMC1L2 belongs to a family of proteins required for chromatid cohesion and DNA recombination during meiosis and mitosis (3:Revenkova et al., 2001 [PubMed 11564881]).[supplied by OMIM, Mar 2008]","start":45344063,"end":45413619,"strand":-1,"description":"structural maintenance of chromosomes 1B [Source:HGNC Symbol;Acc:HGNC:11112]"}, {"versioned_ensembl_gene_id":"ENSG00000130382.8","gene_symbol":"MLLT1","gene_name":"MLLT1, super elongation complex subunit [Source:HGNC Symbol;Acc:HGNC:7134]","synonyms":"YEATS1,LTG19,ENL","biotype":"protein_coding","ncbi_id":"4298","summary":null,"start":6210379,"end":6279948,"strand":-1,"description":"MLLT1, super elongation complex subunit [Source:HGNC Symbol;Acc:HGNC:7134]"}, {"versioned_ensembl_gene_id":"ENSG00000204025.7","gene_symbol":"TRPC5OS","gene_name":"TRPC5 opposite strand [Source:HGNC Symbol;Acc:HGNC:40593]","synonyms":"TRPC5-AS1","biotype":"protein_coding","ncbi_id":"100329135","summary":null,"start":111876051,"end":111903990,"strand":1,"description":"TRPC5 opposite strand [Source:HGNC Symbol;Acc:HGNC:40593]"}, {"versioned_ensembl_gene_id":"ENSG00000237370.1","gene_symbol":"AC010907.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3603397,"end":3604242,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282812.1","gene_symbol":"TRBV28","gene_name":"T-cell receptor beta variable 28 [Source:HGNC Symbol;Acc:HGNC:12209]","synonyms":"TCRBV3S1,TCRBV28S1","biotype":"TR_V_gene","ncbi_id":"28559","summary":null,"start":142761362,"end":142761862,"strand":1,"description":"T-cell receptor beta variable 28 [Source:HGNC Symbol;Acc:HGNC:12209]"}, {"versioned_ensembl_gene_id":"ENSG00000221972.3","gene_symbol":"C3orf36","gene_name":"chromosome 3 open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:26170]","synonyms":"FLJ22173","biotype":"protein_coding","ncbi_id":"80111","summary":null,"start":133928145,"end":133929812,"strand":-1,"description":"chromosome 3 open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:26170]"}, {"versioned_ensembl_gene_id":"ENSG00000280300.1","gene_symbol":"AC117503.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":123754246,"end":123754794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138738.10","gene_symbol":"PRDM5","gene_name":"PR/SET domain 5 [Source:HGNC Symbol;Acc:HGNC:9349]","synonyms":"PFM2","biotype":"protein_coding","ncbi_id":"11107","summary":"The protein encoded by this gene is a transcription factor of the PR-domain protein family. It contains a PR-domain and multiple zinc finger motifs. Transcription factors of the PR-domain family are known to be involved in cell differentiation and tumorigenesis. [provided by RefSeq, Jul 2008]","start":120684919,"end":120922870,"strand":-1,"description":"PR/SET domain 5 [Source:HGNC Symbol;Acc:HGNC:9349]"}, {"versioned_ensembl_gene_id":"ENSG00000235825.3","gene_symbol":"FAM90A9P","gene_name":"family with sequence similarity 90 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:32257]","synonyms":"FAM90A9","biotype":"unprocessed_pseudogene","ncbi_id":"441327","summary":"FAM90A9 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7761330,"end":7764340,"strand":1,"description":"family with sequence similarity 90 member A9, pseudogene [Source:HGNC Symbol;Acc:HGNC:32257]"}, {"versioned_ensembl_gene_id":"ENSG00000258271.1","gene_symbol":"AC025260.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93529560,"end":93529989,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232226.2","gene_symbol":"ARSFP1","gene_name":"arylsulfatase F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:722]","synonyms":"ARSFP","biotype":"unprocessed_pseudogene","ncbi_id":"23757","summary":null,"start":12252321,"end":12258033,"strand":-1,"description":"arylsulfatase F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:722]"}, {"versioned_ensembl_gene_id":"ENSG00000274045.1","gene_symbol":"AC008746.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54445939,"end":54446275,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198858.9","gene_symbol":"R3HDM4","gene_name":"R3H domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28270]","synonyms":"C19orf22,MGC16353","biotype":"protein_coding","ncbi_id":"91300","summary":null,"start":896503,"end":913245,"strand":-1,"description":"R3H domain containing 4 [Source:HGNC Symbol;Acc:HGNC:28270]"}, {"versioned_ensembl_gene_id":"ENSG00000249216.1","gene_symbol":"AC105389.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41688858,"end":41692797,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145476.15","gene_symbol":"CYP4V2","gene_name":"cytochrome P450 family 4 subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:23198]","synonyms":"CYP4AH1","biotype":"protein_coding","ncbi_id":"285440","summary":"This gene encodes a member of the cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy. [provided by RefSeq, Jul 2008]","start":186191520,"end":186213456,"strand":1,"description":"cytochrome P450 family 4 subfamily V member 2 [Source:HGNC Symbol;Acc:HGNC:23198]"}, {"versioned_ensembl_gene_id":"ENSG00000239677.6","gene_symbol":"PDZRN3-AS1","gene_name":"PDZRN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40814]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927249","summary":null,"start":73621713,"end":73626796,"strand":1,"description":"PDZRN3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40814]"}, {"versioned_ensembl_gene_id":"ENSG00000162300.11","gene_symbol":"ZFPL1","gene_name":"zinc finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:12868]","synonyms":"MCG4,D11S750","biotype":"protein_coding","ncbi_id":"7542","summary":null,"start":65084223,"end":65088400,"strand":1,"description":"zinc finger protein like 1 [Source:HGNC Symbol;Acc:HGNC:12868]"}, {"versioned_ensembl_gene_id":"ENSG00000169251.12","gene_symbol":"NMD3","gene_name":"NMD3 ribosome export adaptor [Source:HGNC Symbol;Acc:HGNC:24250]","synonyms":"CGI-07","biotype":"protein_coding","ncbi_id":"51068","summary":"Ribosomal 40S and 60S subunits associate in the nucleolus and are exported to the cytoplasm. The protein encoded by this gene is involved in the passage of the 60S subunit through the nuclear pore complex and into the cytoplasm. Several transcript variants exist for this gene, but the full-length natures of only two have been described to date. [provided by RefSeq, Feb 2016]","start":161104696,"end":161253532,"strand":1,"description":"NMD3 ribosome export adaptor [Source:HGNC Symbol;Acc:HGNC:24250]"}, {"versioned_ensembl_gene_id":"ENSG00000267563.1","gene_symbol":"AC011471.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6259157,"end":6259799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226494.1","gene_symbol":"RPL7P4","gene_name":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]","synonyms":"Em:AB023049.2","biotype":"processed_pseudogene","ncbi_id":"100133037","summary":null,"start":30741465,"end":30742194,"strand":-1,"description":"ribosomal protein L7 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:21634]"}, {"versioned_ensembl_gene_id":"ENSG00000134108.12","gene_symbol":"ARL8B","gene_name":"ADP ribosylation factor like GTPase 8B [Source:HGNC Symbol;Acc:HGNC:25564]","synonyms":"Gie1,FLJ10702,ARL10C","biotype":"protein_coding","ncbi_id":"55207","summary":null,"start":5122220,"end":5180912,"strand":1,"description":"ADP ribosylation factor like GTPase 8B [Source:HGNC Symbol;Acc:HGNC:25564]"}, {"versioned_ensembl_gene_id":"ENSG00000223714.1","gene_symbol":"AL109797.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41275739,"end":41276778,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230913.1","gene_symbol":"NPM1P51","gene_name":"nucleophosmin 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:45230]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130606","summary":null,"start":41666906,"end":41667649,"strand":1,"description":"nucleophosmin 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:45230]"}, {"versioned_ensembl_gene_id":"ENSG00000237613.2","gene_symbol":"FAM138A","gene_name":"family with sequence similarity 138 member A [Source:HGNC Symbol;Acc:HGNC:32334]","synonyms":"F379","biotype":"lincRNA","ncbi_id":"645520","summary":null,"start":34554,"end":36081,"strand":-1,"description":"family with sequence similarity 138 member A [Source:HGNC Symbol;Acc:HGNC:32334]"}, {"versioned_ensembl_gene_id":"ENSG00000240549.2","gene_symbol":"THOC7-AS1","gene_name":"THOC7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41249]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874039","summary":null,"start":63860645,"end":63861819,"strand":1,"description":"THOC7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41249]"}, {"versioned_ensembl_gene_id":"ENSG00000081923.11","gene_symbol":"ATP8B1","gene_name":"ATPase phospholipid transporting 8B1 [Source:HGNC Symbol;Acc:HGNC:3706]","synonyms":"PFIC1,PFIC,FIC1,BRIC,ATPIC","biotype":"protein_coding","ncbi_id":"5205","summary":"This gene encodes a member of the P-type cation transport ATPase family, which belongs to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis. [provided by RefSeq, Jul 2008]","start":57646426,"end":57803101,"strand":-1,"description":"ATPase phospholipid transporting 8B1 [Source:HGNC Symbol;Acc:HGNC:3706]"}, {"versioned_ensembl_gene_id":"ENSG00000235215.2","gene_symbol":"AL592431.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59055999,"end":59078116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000064042.17","gene_symbol":"LIMCH1","gene_name":"LIM and calponin homology domains 1 [Source:HGNC Symbol;Acc:HGNC:29191]","synonyms":"LMO7B,LIMCH1A,DKFZP686A01247","biotype":"protein_coding","ncbi_id":"22998","summary":null,"start":41359607,"end":41700044,"strand":1,"description":"LIM and calponin homology domains 1 [Source:HGNC Symbol;Acc:HGNC:29191]"}, {"versioned_ensembl_gene_id":"ENSG00000241042.1","gene_symbol":"AL592431.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59054397,"end":59056049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173432.10","gene_symbol":"SAA1","gene_name":"serum amyloid A1 [Source:HGNC Symbol;Acc:HGNC:10513]","synonyms":"TP53I4,SAA,PIG4","biotype":"protein_coding","ncbi_id":"6288","summary":"This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. Alternate splicing results in multiple transcript variants that encode the same protein. A pseudogene of this gene is found on chromosome 11. [provided by RefSeq, Jul 2020]","start":18266174,"end":18269977,"strand":1,"description":"serum amyloid A1 [Source:HGNC Symbol;Acc:HGNC:10513]"}, {"versioned_ensembl_gene_id":"ENSG00000271421.1","gene_symbol":"AC005191.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111930735,"end":111931092,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237352.3","gene_symbol":"LINC01358","gene_name":"long intergenic non-protein coding RNA 1358 [Source:HGNC Symbol;Acc:HGNC:50589]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101926925","summary":null,"start":58933643,"end":59240555,"strand":1,"description":"long intergenic non-protein coding RNA 1358 [Source:HGNC Symbol;Acc:HGNC:50589]"}, {"versioned_ensembl_gene_id":"ENSG00000072315.3","gene_symbol":"TRPC5","gene_name":"transient receptor potential cation channel subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:12337]","synonyms":"PPP1R159","biotype":"protein_coding","ncbi_id":"7224","summary":"This gene belongs to the transient receptor family. It encodes one of the seven mammalian TRPC (transient receptor potential channel) proteins. The encoded protein is a multi-pass membrane protein and is thought to form a receptor-activated non-selective calcium permeant cation channel. The protein is active alone or as a heteromultimeric assembly with TRPC1, TRPC3, and TRPC4. It also interacts with multiple proteins including calmodulin, CABP1, enkurin, Na(+)-H+ exchange regulatory factor (NHERF ), interferon-induced GTP-binding protein (MX1), ring finger protein 24 (RNF24), and SEC14 domain and spectrin repeat-containing protein 1 (SESTD1). [provided by RefSeq, May 2010]","start":111774315,"end":112082776,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 5 [Source:HGNC Symbol;Acc:HGNC:12337]"}, {"versioned_ensembl_gene_id":"ENSG00000251498.1","gene_symbol":"AC021146.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68972999,"end":68975993,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280212.1","gene_symbol":"AC012254.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":47076117,"end":47076594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224479.6","gene_symbol":"AC104162.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":63741827,"end":63827445,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253284.2","gene_symbol":"AC092828.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":19147074,"end":19154659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281571.2","gene_symbol":"AC241585.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":145214851,"end":145215938,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167216.16","gene_symbol":"KATNAL2","gene_name":"katanin catalytic subunit A1 like 2 [Source:HGNC Symbol;Acc:HGNC:25387]","synonyms":"MGC33211,DKFZP667C165","biotype":"protein_coding","ncbi_id":"83473","summary":null,"start":46917492,"end":47102243,"strand":1,"description":"katanin catalytic subunit A1 like 2 [Source:HGNC Symbol;Acc:HGNC:25387]"}, {"versioned_ensembl_gene_id":"ENSG00000272419.6","gene_symbol":"AC241585.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":145164099,"end":145216058,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000052126.14","gene_symbol":"PLEKHA5","gene_name":"pleckstrin homology domain containing A5 [Source:HGNC Symbol;Acc:HGNC:30036]","synonyms":"KIAA1686,FLJ10667,PEPP2","biotype":"protein_coding","ncbi_id":"54477","summary":null,"start":19129752,"end":19376400,"strand":1,"description":"pleckstrin homology domain containing A5 [Source:HGNC Symbol;Acc:HGNC:30036]"}, {"versioned_ensembl_gene_id":"ENSG00000166986.14","gene_symbol":"MARS","gene_name":"methionyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6898]","synonyms":"SPG70,MetRS,CMT2U","biotype":"protein_coding","ncbi_id":"4141","summary":"This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. The encoded protein is a component of the multi-tRNA synthetase complex and catalyzes the ligation of methionine to tRNA molecules. [provided by RefSeq, Jan 2011]","start":57475445,"end":57517569,"strand":1,"description":"methionyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:6898]"}, {"versioned_ensembl_gene_id":"ENSG00000275736.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094679,"end":54102746,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000231125.2","gene_symbol":"AF129075.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":29058073,"end":29060095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156261.12","gene_symbol":"CCT8","gene_name":"chaperonin containing TCP1 subunit 8 [Source:HGNC Symbol;Acc:HGNC:1623]","synonyms":"PRED71,Cctq,C21orf112","biotype":"protein_coding","ncbi_id":"10694","summary":"This gene encodes the theta subunit of the CCT chaperonin, which is abundant in the eukaryotic cytosol and may be involved in the transport and assembly of newly synthesized proteins. Alternative splicing results in multiple transcript variants of this gene. A pseudogene related to this gene is located on chromosome 1. [provided by RefSeq, Sep 2013]","start":29055805,"end":29073797,"strand":-1,"description":"chaperonin containing TCP1 subunit 8 [Source:HGNC Symbol;Acc:HGNC:1623]"}, {"versioned_ensembl_gene_id":"ENSG00000228121.1","gene_symbol":"PHBP3","gene_name":"prohibitin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:8915]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391044","summary":null,"start":58999676,"end":59000494,"strand":1,"description":"prohibitin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:8915]"}, {"versioned_ensembl_gene_id":"ENSG00000224609.6","gene_symbol":"HSD52","gene_name":"uncharacterized LOC729467 [Source:NCBI gene;Acc:729467]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"729467","summary":null,"start":59131936,"end":59208121,"strand":-1,"description":"uncharacterized LOC729467 [Source:NCBI gene;Acc:729467]"}, {"versioned_ensembl_gene_id":"ENSG00000249735.1","gene_symbol":"AC021146.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":68985009,"end":68988533,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147536.11","gene_symbol":"GINS4","gene_name":"GINS complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:28226]","synonyms":"SLD5,MGC14799","biotype":"protein_coding","ncbi_id":"84296","summary":"The yeast heterotetrameric GINS complex is made up of Sld5, Psf1 (GINS1; MIM 610608), Psf2 (GINS2; MIM 610609), and Psf3 (GINS3; MIM 610610). The formation of the GINS complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]). See GINS1 for additional information about the GINS complex.[supplied by OMIM, Mar 2008]","start":41529206,"end":41545046,"strand":1,"description":"GINS complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:28226]"}, {"versioned_ensembl_gene_id":"ENSG00000225846.4","gene_symbol":"AC112719.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76036750,"end":76037064,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245711.2","gene_symbol":"NADK2-AS1","gene_name":"NADK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41143]","synonyms":"NADKD1-AS1","biotype":"antisense_RNA","ncbi_id":"101056700","summary":null,"start":36221055,"end":36221902,"strand":1,"description":"NADK2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41143]"}, {"versioned_ensembl_gene_id":"ENSG00000180205.3","gene_symbol":"WFDC9","gene_name":"WAP four-disulfide core domain 9 [Source:HGNC Symbol;Acc:HGNC:20380]","synonyms":"WAP9,dJ688G8.2","biotype":"protein_coding","ncbi_id":"259240","summary":"The WAP-type four-disulfide core (WFDC) domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many members of the WFDC domain family. This gene encodes a protein which contains a WFDC domain, and is thus a member of the WFDC domain family. This gene and several other gene family members are clustered at 20q13.12. [provided by RefSeq, Jul 2008]","start":45607939,"end":45631268,"strand":-1,"description":"WAP four-disulfide core domain 9 [Source:HGNC Symbol;Acc:HGNC:20380]"}, {"versioned_ensembl_gene_id":"ENSG00000169245.5","gene_symbol":"CXCL10","gene_name":"C-X-C motif chemokine ligand 10 [Source:HGNC Symbol;Acc:HGNC:10637]","synonyms":"SCYB10,mob-1,IP-10,INP10,IFI10,gIP-10,crg-2,C7","biotype":"protein_coding","ncbi_id":"3627","summary":"This antimicrobial gene encodes a chemokine of the CXC subfamily and ligand for the receptor CXCR3. Binding of this protein to CXCR3 results in pleiotropic effects, including stimulation of monocytes, natural killer and T-cell migration, and modulation of adhesion molecule expression. This gene may also be a key regulator of the 'cytokine storm' immune response to SARS-CoV-2 infection. [provided by RefSeq, Sep 2020]","start":76021117,"end":76023497,"strand":-1,"description":"C-X-C motif chemokine ligand 10 [Source:HGNC Symbol;Acc:HGNC:10637]"}, {"versioned_ensembl_gene_id":"ENSG00000226525.5","gene_symbol":"RPS7P10","gene_name":"ribosomal protein S7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39903]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128060","summary":null,"start":21628413,"end":21629015,"strand":-1,"description":"ribosomal protein S7 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39903]"}, {"versioned_ensembl_gene_id":"ENSG00000267040.6","gene_symbol":"AC027097.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57630302,"end":57669296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163632.12","gene_symbol":"C3orf49","gene_name":"chromosome 3 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:25190]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132200","summary":null,"start":63819362,"end":63848636,"strand":1,"description":"chromosome 3 open reading frame 49 [Source:HGNC Symbol;Acc:HGNC:25190]"}, {"versioned_ensembl_gene_id":"ENSG00000180964.16","gene_symbol":"TCEAL8","gene_name":"transcription elongation factor A like 8 [Source:HGNC Symbol;Acc:HGNC:28683]","synonyms":"WEX3,MGC45400","biotype":"protein_coding","ncbi_id":"90843","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]","start":103252995,"end":103255203,"strand":-1,"description":"transcription elongation factor A like 8 [Source:HGNC Symbol;Acc:HGNC:28683]"}, {"versioned_ensembl_gene_id":"ENSG00000267787.5","gene_symbol":"AC027097.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57639455,"end":57738044,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271642.1","gene_symbol":"MARK3P1","gene_name":"microtubule affinity regulating kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50312]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421550","summary":null,"start":46682071,"end":46682713,"strand":-1,"description":"microtubule affinity regulating kinase 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50312]"}, {"versioned_ensembl_gene_id":"ENSG00000188177.13","gene_symbol":"ZC3H6","gene_name":"zinc finger CCCH-type containing 6 [Source:HGNC Symbol;Acc:HGNC:24762]","synonyms":"ZC3HDC6,KIAA2035,FLJ45877,FLJ41410","biotype":"protein_coding","ncbi_id":"376940","summary":null,"start":112275594,"end":112340063,"strand":1,"description":"zinc finger CCCH-type containing 6 [Source:HGNC Symbol;Acc:HGNC:24762]"}, {"versioned_ensembl_gene_id":"ENSG00000257496.1","gene_symbol":"AC025031.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46384233,"end":46386991,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250277.2","gene_symbol":"AC021146.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68996935,"end":68997709,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164344.15","gene_symbol":"KLKB1","gene_name":"kallikrein B1 [Source:HGNC Symbol;Acc:HGNC:6371]","synonyms":"KLK3","biotype":"protein_coding","ncbi_id":"3818","summary":"This gene encodes a glycoprotein that participates in the surface-dependent activation of blood coagulation, fibrinolysis, kinin generation and inflammation. The encoded preproprotein present in plasma as a non-covalent complex with high molecular weight kininogen undergoes proteolytic processing mediated by activated coagulation factor XII to generate a disulfide-linked, heterodimeric serine protease comprised of heavy and light chains. Certain mutations in this gene cause prekallikrein deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]","start":186208979,"end":186258471,"strand":1,"description":"kallikrein B1 [Source:HGNC Symbol;Acc:HGNC:6371]"}, {"versioned_ensembl_gene_id":"ENSG00000169248.12","gene_symbol":"CXCL11","gene_name":"C-X-C motif chemokine ligand 11 [Source:HGNC Symbol;Acc:HGNC:10638]","synonyms":"b-R1,SCYB9B,SCYB11,IP-9,I-TAC,H174","biotype":"protein_coding","ncbi_id":"6373","summary":"Chemokines are a group of small (approximately 8 to 14 kD), mostly basic, structurally related molecules that regulate cell trafficking of various types of leukocytes through interactions with a subset of 7-transmembrane, G protein-coupled receptors. Chemokines also play fundamental roles in the development, homeostasis, and function of the immune system, and they have effects on cells of the central nervous system as well as on endothelial cells involved in angiogenesis or angiostasis. Chemokines are divided into 2 major subfamilies, CXC and CC. This antimicrobial gene is a CXC member of the chemokine superfamily. Its encoded protein induces a chemotactic response in activated T-cells and is the dominant ligand for CXC receptor-3. The gene encoding this protein contains 4 exons and at least three polyadenylation signals which might reflect cell-specific regulation of expression. IFN-gamma is a potent inducer of transcription of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]","start":76033682,"end":76041415,"strand":-1,"description":"C-X-C motif chemokine ligand 11 [Source:HGNC Symbol;Acc:HGNC:10638]"}, {"versioned_ensembl_gene_id":"ENSG00000278896.1","gene_symbol":"AC025031.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46404644,"end":46407166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180305.4","gene_symbol":"WFDC10A","gene_name":"WAP four-disulfide core domain 10A [Source:HGNC Symbol;Acc:HGNC:16139]","synonyms":"WAP10,dJ688G8.3,C20orf146","biotype":"protein_coding","ncbi_id":"140832","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008]","start":45629526,"end":45631196,"strand":1,"description":"WAP four-disulfide core domain 10A [Source:HGNC Symbol;Acc:HGNC:16139]"}, {"versioned_ensembl_gene_id":"ENSG00000257261.5","gene_symbol":"AC008014.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46383679,"end":46876159,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261618.1","gene_symbol":"AC083837.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":78837529,"end":78840522,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223558.1","gene_symbol":"TRIM60P17","gene_name":"tripartite motif containing 60 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38489]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420414","summary":null,"start":64085560,"end":64086576,"strand":1,"description":"tripartite motif containing 60 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:38489]"}, {"versioned_ensembl_gene_id":"ENSG00000253659.1","gene_symbol":"AC138646.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":79297717,"end":79314471,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225116.1","gene_symbol":"AL353193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3465177,"end":3465444,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139083.10","gene_symbol":"ETV6","gene_name":"ETS variant 6 [Source:HGNC Symbol;Acc:HGNC:3495]","synonyms":"TEL","biotype":"protein_coding","ncbi_id":"2120","summary":"This gene encodes an ETS family transcription factor. The product of this gene contains two functional domains: a N-terminal pointed (PNT) domain that is involved in protein-protein interactions with itself and other proteins, and a C-terminal DNA-binding domain. Gene knockout studies in mice suggest that it is required for hematopoiesis and maintenance of the developing vascular network. This gene is known to be involved in a large number of chromosomal rearrangements associated with leukemia and congenital fibrosarcoma. [provided by RefSeq, Sep 2008]","start":11649854,"end":11895402,"strand":1,"description":"ETS variant 6 [Source:HGNC Symbol;Acc:HGNC:3495]"}, {"versioned_ensembl_gene_id":"ENSG00000236826.7","gene_symbol":"LSM2","gene_name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]","synonyms":"C6orf28,YBL026W,G7b","biotype":"protein_coding","ncbi_id":"57819","summary":"This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]","start":31784754,"end":31794345,"strand":-1,"description":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Source:HGNC Symbol;Acc:HGNC:13940]"}, {"versioned_ensembl_gene_id":"ENSG00000139209.15","gene_symbol":"SLC38A4","gene_name":"solute carrier family 38 member 4 [Source:HGNC Symbol;Acc:HGNC:14679]","synonyms":"PAAT,NAT3,ATA3","biotype":"protein_coding","ncbi_id":"55089","summary":"SLC38A4 is found predominantly in liver and transports both cationic and neutral amino acids. The transport of cationic amino acids by SLC38A4 is Na(+) and pH independent, while the transport of neutral amino acids is Na(+) and pH dependent (Hatanaka et al., 2001 [PubMed 11342143]).[supplied by OMIM, Mar 2008]","start":46764761,"end":46832408,"strand":-1,"description":"solute carrier family 38 member 4 [Source:HGNC Symbol;Acc:HGNC:14679]"}, {"versioned_ensembl_gene_id":"ENSG00000163634.11","gene_symbol":"THOC7","gene_name":"THO complex 7 [Source:HGNC Symbol;Acc:HGNC:29874]","synonyms":"NIF3L1BP1,fSAP24,FLJ23445","biotype":"protein_coding","ncbi_id":"80145","summary":null,"start":63833870,"end":63863903,"strand":-1,"description":"THO complex 7 [Source:HGNC Symbol;Acc:HGNC:29874]"}, {"versioned_ensembl_gene_id":"ENSG00000251685.3","gene_symbol":"UGT2B27P","gene_name":"UDP glucuronosyltransferase family 2 member B27, pseudogene [Source:HGNC Symbol;Acc:HGNC:12551]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"54569","summary":null,"start":69004862,"end":69020414,"strand":-1,"description":"UDP glucuronosyltransferase family 2 member B27, pseudogene [Source:HGNC Symbol;Acc:HGNC:12551]"}, {"versioned_ensembl_gene_id":"ENSG00000163751.3","gene_symbol":"CPA3","gene_name":"carboxypeptidase A3 [Source:HGNC Symbol;Acc:HGNC:2298]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1359","summary":"This gene encodes a member of the carboxypeptidase A family of zinc metalloproteases. The encoded preproprotein is proteolytically processed to generate a mature protease that is released by mast cells and may be involved in the degradation of endogenous proteins and the inactivation of venom-associated peptides. Expression of this gene may be elevated in human asthma patients. [provided by RefSeq, Nov 2015]","start":148865256,"end":148897196,"strand":1,"description":"carboxypeptidase A3 [Source:HGNC Symbol;Acc:HGNC:2298]"}, {"versioned_ensembl_gene_id":"ENSG00000235258.1","gene_symbol":"NDUFB4P6","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45254]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075097","summary":null,"start":112286057,"end":112286422,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45254]"}, {"versioned_ensembl_gene_id":"ENSG00000214684.2","gene_symbol":"AC003045.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117439982,"end":117440780,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268509.2","gene_symbol":"AC026202.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5187172,"end":5188298,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134109.10","gene_symbol":"EDEM1","gene_name":"ER degradation enhancing alpha-mannosidase like protein 1 [Source:HGNC Symbol;Acc:HGNC:18967]","synonyms":"KIAA0212,EDEM","biotype":"protein_coding","ncbi_id":"9695","summary":null,"start":5187646,"end":5219957,"strand":1,"description":"ER degradation enhancing alpha-mannosidase like protein 1 [Source:HGNC Symbol;Acc:HGNC:18967]"}, {"versioned_ensembl_gene_id":"ENSG00000132819.16","gene_symbol":"RBM38","gene_name":"RNA binding motif protein 38 [Source:HGNC Symbol;Acc:HGNC:15818]","synonyms":"SEB4D,seb4B,RNPC1,HSRNASEB,dJ800J21.2","biotype":"protein_coding","ncbi_id":"55544","summary":null,"start":57391407,"end":57409333,"strand":1,"description":"RNA binding motif protein 38 [Source:HGNC Symbol;Acc:HGNC:15818]"}, {"versioned_ensembl_gene_id":"ENSG00000102678.6","gene_symbol":"FGF9","gene_name":"fibroblast growth factor 9 [Source:HGNC Symbol;Acc:HGNC:3687]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2254","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein was isolated as a secreted factor that exhibits a growth-stimulating effect on cultured glial cells. In nervous system, this protein is produced mainly by neurons and may be important for glial cell development. Expression of the mouse homolog of this gene was found to be dependent on Sonic hedgehog (Shh) signaling. Mice lacking the homolog gene displayed a male-to-female sex reversal phenotype, which suggested a role in testicular embryogenesis. [provided by RefSeq, Jul 2008]","start":21671383,"end":21704498,"strand":1,"description":"fibroblast growth factor 9 [Source:HGNC Symbol;Acc:HGNC:3687]"}, {"versioned_ensembl_gene_id":"ENSG00000148942.14","gene_symbol":"SLC5A12","gene_name":"solute carrier family 5 member 12 [Source:HGNC Symbol;Acc:HGNC:28750]","synonyms":"SMCT2,MGC52019","biotype":"protein_coding","ncbi_id":"159963","summary":"Normal blood lactate is maintained at about 1.5 mM, and little filtered lactate is excreted in urine. Reabsorption of lactate is mediated by the low-affinity Na(+)-coupled lactate transporter SLC5A12 in the initial part of the proximal tubule and by the high-affinity Na(+)-coupled lactate transporter SLC5A8 (MIM 608044) in the distal proximal tubule (Gopal et al., 2007 [PubMed 17692818]).[supplied by OMIM, Dec 2008]","start":26667019,"end":26723427,"strand":-1,"description":"solute carrier family 5 member 12 [Source:HGNC Symbol;Acc:HGNC:28750]"}, {"versioned_ensembl_gene_id":"ENSG00000167632.14","gene_symbol":"TRAPPC9","gene_name":"trafficking protein particle complex 9 [Source:HGNC Symbol;Acc:HGNC:30832]","synonyms":"TRS120,T1,NIBP,MRT13,KIAA1882,IKBKBBP","biotype":"protein_coding","ncbi_id":"83696","summary":"This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]","start":139730343,"end":140458579,"strand":-1,"description":"trafficking protein particle complex 9 [Source:HGNC Symbol;Acc:HGNC:30832]"}, {"versioned_ensembl_gene_id":"ENSG00000129195.15","gene_symbol":"PIMREG","gene_name":"PICALM interacting mitotic regulator [Source:HGNC Symbol;Acc:HGNC:25483]","synonyms":"FLJ10491,FLJ10156,FAM64A,CATS,RCS1","biotype":"protein_coding","ncbi_id":"54478","summary":null,"start":6444415,"end":6451469,"strand":1,"description":"PICALM interacting mitotic regulator [Source:HGNC Symbol;Acc:HGNC:25483]"}, {"versioned_ensembl_gene_id":"ENSG00000187066.8","gene_symbol":"TMEM262","gene_name":"transmembrane protein 262 [Source:HGNC Symbol;Acc:HGNC:49389]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100130348","summary":null,"start":65084979,"end":65089375,"strand":-1,"description":"transmembrane protein 262 [Source:HGNC Symbol;Acc:HGNC:49389]"}, {"versioned_ensembl_gene_id":"ENSG00000230252.1","gene_symbol":"MTND2P4","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42105]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873175","summary":null,"start":64110547,"end":64111550,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:42105]"}, {"versioned_ensembl_gene_id":"ENSG00000227035.1","gene_symbol":"MTATP6P18","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52063]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075159","summary":null,"start":64106822,"end":64107572,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:52063]"}, {"versioned_ensembl_gene_id":"ENSG00000253174.2","gene_symbol":"AC009630.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41540381,"end":41545044,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230052.1","gene_symbol":"MTND3P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42142]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873180","summary":null,"start":64105654,"end":64105995,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42142]"}, {"versioned_ensembl_gene_id":"ENSG00000273998.1","gene_symbol":"AL049794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16576068,"end":16579615,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233385.1","gene_symbol":"MTCO3P8","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52038]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075151","summary":null,"start":64106065,"end":64106819,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52038]"}, {"versioned_ensembl_gene_id":"ENSG00000229881.1","gene_symbol":"AC091685.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64140495,"end":64150058,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253133.1","gene_symbol":"AC009630.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41534155,"end":41578368,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275728.1","gene_symbol":"AL049794.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16580258,"end":16580622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248315.1","gene_symbol":"MTND4LP2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42236]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075098","summary":null,"start":64105292,"end":64105576,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42236]"}, {"versioned_ensembl_gene_id":"ENSG00000224458.3","gene_symbol":"GUSBP6","gene_name":"glucuronidase, beta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42320]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653435","summary":null,"start":64100305,"end":64150721,"strand":1,"description":"glucuronidase, beta pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42320]"}, {"versioned_ensembl_gene_id":"ENSG00000226229.2","gene_symbol":"RPLP0P1","gene_name":"ribosomal protein lateral stalk subunit P0 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16585]","synonyms":"dJ777L9.2","biotype":"processed_pseudogene","ncbi_id":"128745","summary":null,"start":16586333,"end":16586693,"strand":-1,"description":"ribosomal protein lateral stalk subunit P0 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16585]"}, {"versioned_ensembl_gene_id":"ENSG00000264578.1","gene_symbol":"AC009630.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41609692,"end":41621502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235208.2","gene_symbol":"AL135938.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16684108,"end":16684404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236976.1","gene_symbol":"AC091685.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64141538,"end":64142401,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153002.11","gene_symbol":"CPB1","gene_name":"carboxypeptidase B1 [Source:HGNC Symbol;Acc:HGNC:2299]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1360","summary":"Three different procarboxypeptidases A and two different procarboxypeptidases B have been isolated. The B1 and B2 forms differ from each other mainly in isoelectric point. Carboxypeptidase B1 is a highly tissue-specific protein and is a useful serum marker for acute pancreatitis and dysfunction of pancreatic transplants. It is not elevated in pancreatic carcinoma. [provided by RefSeq, Jul 2008]","start":148791102,"end":148860187,"strand":1,"description":"carboxypeptidase B1 [Source:HGNC Symbol;Acc:HGNC:2299]"}, {"versioned_ensembl_gene_id":"ENSG00000235646.1","gene_symbol":"MTND1P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42051]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873170","summary":null,"start":64111752,"end":64112572,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42051]"}, {"versioned_ensembl_gene_id":"ENSG00000120833.13","gene_symbol":"SOCS2","gene_name":"suppressor of cytokine signaling 2 [Source:HGNC Symbol;Acc:HGNC:19382]","synonyms":"SOCS-2,Cish2,CIS2,STATI2,SSI2,SSI-2","biotype":"protein_coding","ncbi_id":"8835","summary":"This gene encodes a member of the suppressor of cytokine signaling (SOCS) family. SOCS family members are cytokine-inducible negative regulators of cytokine receptor signaling via the Janus kinase/signal transducer and activation of transcription pathway (the JAK/STAT pathway). SOCS family proteins interact with major molecules of signaling complexes to block further signal transduction, in part, by proteasomal depletion of receptors or signal-transducing proteins via ubiquitination. The expression of this gene can be induced by a subset of cytokines, including erythropoietin, GM-CSF, IL10, interferon (IFN)-gamma and by cytokine receptors such as growth horomone receptor. The protein encoded by this gene interacts with the cytoplasmic domain of insulin-like growth factor-1 receptor (IGF1R) and is thought to be involved in the regulation of IGF1R mediated cell signaling. This gene has pseudogenes on chromosomes 20 and 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":93569814,"end":93583487,"strand":1,"description":"suppressor of cytokine signaling 2 [Source:HGNC Symbol;Acc:HGNC:19382]"}, {"versioned_ensembl_gene_id":"ENSG00000248704.1","gene_symbol":"MTND4P2","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42189]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873188","summary":null,"start":64104093,"end":64105295,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42189]"}, {"versioned_ensembl_gene_id":"ENSG00000253391.1","gene_symbol":"AC100870.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":79520145,"end":79520649,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234700.1","gene_symbol":"MTCO1P8","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52010]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075138","summary":null,"start":64108625,"end":64110147,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52010]"}, {"versioned_ensembl_gene_id":"ENSG00000240540.2","gene_symbol":"RPL3P9","gene_name":"ribosomal protein L3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36839]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128963","summary":null,"start":79571153,"end":79572335,"strand":-1,"description":"ribosomal protein L3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:36839]"}, {"versioned_ensembl_gene_id":"ENSG00000213643.3","gene_symbol":"VN1R37P","gene_name":"vomeronasal 1 receptor 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:37357]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402273","summary":null,"start":64149685,"end":64150432,"strand":-1,"description":"vomeronasal 1 receptor 37 pseudogene [Source:HGNC Symbol;Acc:HGNC:37357]"}, {"versioned_ensembl_gene_id":"ENSG00000225963.7","gene_symbol":"AC009950.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":230121370,"end":230174223,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234234.1","gene_symbol":"MTCO2P8","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52024]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075146","summary":null,"start":64107829,"end":64108486,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:52024]"}, {"versioned_ensembl_gene_id":"ENSG00000125870.10","gene_symbol":"SNRPB2","gene_name":"small nuclear ribonucleoprotein polypeptide B2 [Source:HGNC Symbol;Acc:HGNC:11155]","synonyms":"U2B'',Msl1","biotype":"protein_coding","ncbi_id":"6629","summary":"The protein encoded by this gene associates with stem loop IV of U2 small nuclear ribonucleoprotein (U2 snRNP) in the presence of snRNP-A'. The encoded protein may play a role in pre-mRNA splicing. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":16729961,"end":16742563,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide B2 [Source:HGNC Symbol;Acc:HGNC:11155]"}, {"versioned_ensembl_gene_id":"ENSG00000149809.14","gene_symbol":"TM7SF2","gene_name":"transmembrane 7 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11863]","synonyms":"NET47,DHCR14A,ANG1","biotype":"protein_coding","ncbi_id":"7108","summary":null,"start":65111845,"end":65116384,"strand":1,"description":"transmembrane 7 superfamily member 2 [Source:HGNC Symbol;Acc:HGNC:11863]"}, {"versioned_ensembl_gene_id":"ENSG00000276121.1","gene_symbol":"AC122108.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44778196,"end":44778721,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163867.16","gene_symbol":"ZMYM6","gene_name":"zinc finger MYM-type containing 6 [Source:HGNC Symbol;Acc:HGNC:13050]","synonyms":"ZNF258,ZNF198L4,ZBED7,MYM,Buster2","biotype":"protein_coding","ncbi_id":"9204","summary":null,"start":34986165,"end":35031968,"strand":-1,"description":"zinc finger MYM-type containing 6 [Source:HGNC Symbol;Acc:HGNC:13050]"}, {"versioned_ensembl_gene_id":"ENSG00000134698.10","gene_symbol":"AGO4","gene_name":"argonaute 4, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:18424]","synonyms":"KIAA1567,hAGO4,FLJ20033,EIF2C4","biotype":"protein_coding","ncbi_id":"192670","summary":"This gene encodes a member of the Argonaute family of proteins which contain PAZ and PIWI domains and play an integral role in RNA interference and short-interfering-RNA-mediated gene silencing. This gene is located on chromosome 1 in a cluster of related family members. [provided by RefSeq, Mar 2017]","start":35808172,"end":35857890,"strand":1,"description":"argonaute 4, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:18424]"}, {"versioned_ensembl_gene_id":"ENSG00000140623.13","gene_symbol":"SEPT12","gene_name":"septin 12 [Source:HGNC Symbol;Acc:HGNC:26348]","synonyms":"FLJ25410","biotype":"protein_coding","ncbi_id":"124404","summary":"This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":4777669,"end":4788521,"strand":-1,"description":"septin 12 [Source:HGNC Symbol;Acc:HGNC:26348]"}, {"versioned_ensembl_gene_id":"ENSG00000073614.12","gene_symbol":"KDM5A","gene_name":"lysine demethylase 5A [Source:HGNC Symbol;Acc:HGNC:9886]","synonyms":"RBBP2,JARID1A","biotype":"protein_coding","ncbi_id":"5927","summary":"This gene encodes a member of the Jumonji, AT-rich interactive domain 1 (JARID1) histone demethylase protein family. The encoded protein plays a role in gene regulation through the histone code by specifically demethylating lysine 4 of histone H3. The encoded protein interacts with many other proteins, including retinoblastoma protein, and is implicated in the transcriptional regulation of Hox genes and cytokines. This gene may play a role in tumor progression. [provided by RefSeq, Aug 2013]","start":280129,"end":389454,"strand":-1,"description":"lysine demethylase 5A [Source:HGNC Symbol;Acc:HGNC:9886]"}, {"versioned_ensembl_gene_id":"ENSG00000079263.18","gene_symbol":"SP140","gene_name":"SP140 nuclear body protein [Source:HGNC Symbol;Acc:HGNC:17133]","synonyms":"LYSP100-B,LYSP100-A","biotype":"protein_coding","ncbi_id":"11262","summary":"This gene encodes a member of the SP100 family of proteins, which are share common domains including an N-terminal homogeneously staining region domain followed by a SP100/autoimmune regulator/NucP41/P75/deformed epidermal autoregulatory factor domain, a plant homeobox zinc finger, and a bromodomain. The encoded protein is interferon-inducible and is expressed at high levels in the nuclei of leukocytes. Variants of this gene have been associated with multiple sclerosis, Crohn's disease, and chronic lymphocytic leukemia. Alternative splicing results in multiple variants. [provided by RefSeq, Aug 2016]","start":230203110,"end":230313215,"strand":1,"description":"SP140 nuclear body protein [Source:HGNC Symbol;Acc:HGNC:17133]"}, {"versioned_ensembl_gene_id":"ENSG00000102096.9","gene_symbol":"PIM2","gene_name":"Pim-2 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:8987]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11040","summary":"This gene encodes a protooncogene that acts as a serine/threonine protein kinase. Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival.[provided by RefSeq, Nov 2009]","start":48913182,"end":48919024,"strand":-1,"description":"Pim-2 proto-oncogene, serine/threonine kinase [Source:HGNC Symbol;Acc:HGNC:8987]"}, {"versioned_ensembl_gene_id":"ENSG00000128311.13","gene_symbol":"TST","gene_name":"thiosulfate sulfurtransferase [Source:HGNC Symbol;Acc:HGNC:12388]","synonyms":"RDS","biotype":"protein_coding","ncbi_id":"7263","summary":"This is one of two neighboring genes encoding similar proteins that each contain two rhodanese domains. The encoded protein is localized to the mitochondria and catalyzes the conversion of thiosulfate and cyanide to thiocyanate and sulfite. In addition, the protein interacts with 5S ribosomal RNA and facilitates its import into the mitochondria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]","start":37010859,"end":37020183,"strand":-1,"description":"thiosulfate sulfurtransferase [Source:HGNC Symbol;Acc:HGNC:12388]"}, {"versioned_ensembl_gene_id":"ENSG00000218018.2","gene_symbol":"AL109955.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57384160,"end":57393062,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259838.1","gene_symbol":"ELOCP2","gene_name":"elongin C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17762]","synonyms":"TCEB1P2","biotype":"unprocessed_pseudogene","ncbi_id":"283747","summary":null,"start":41557027,"end":41557435,"strand":1,"description":"elongin C pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17762]"}, {"versioned_ensembl_gene_id":"ENSG00000233912.1","gene_symbol":"AC026202.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5156905,"end":5187329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167769.4","gene_symbol":"ACER1","gene_name":"alkaline ceramidase 1 [Source:HGNC Symbol;Acc:HGNC:18356]","synonyms":"ASAH3","biotype":"protein_coding","ncbi_id":"125981","summary":"Ceramides are synthesized during epidermal differentiation and accumulate within the interstices of the stratum corneum, where they represent critical components of the epidermal permeability barrier. Excess cellular ceramide can trigger antimitogenic signals and induce apoptosis, and the ceramide metabolites sphingosine and sphingosine-1-phosphate (S1P) are important bioregulatory molecules. Ceramide hydrolysis in the nucleated cell layers regulates keratinocyte proliferation and apoptosis in response to external stress. Ceramide hydrolysis also occurs at the stratum corneum, releasing free sphingoid base that functions as an endogenous antimicrobial agent. ACER1 is highly expressed in epidermis and catalyzes the hydrolysis of very long chain ceramides to generate sphingosine (Houben et al., 2006 [PubMed 16477081]; Sun et al., 2008 [PubMed 17713573]).[supplied by OMIM, Jul 2010]","start":6306142,"end":6333629,"strand":-1,"description":"alkaline ceramidase 1 [Source:HGNC Symbol;Acc:HGNC:18356]"}, {"versioned_ensembl_gene_id":"ENSG00000184076.13","gene_symbol":"UQCR10","gene_name":"ubiquinol-cytochrome c reductase, complex III subunit X [Source:HGNC Symbol;Acc:HGNC:30863]","synonyms":"UCRC,UCCR7.2,QCR9,HSPC051","biotype":"protein_coding","ncbi_id":"29796","summary":"UCRC is a subunit of mitochondrial complex III (ubiquinol-cytochrome c reductase; EC 1.10.2.2), which forms the middle segment of the respiratory chain of the inner mitochondrial membrane (Schagger et al., 1995 [PubMed 8592474]).[supplied by OMIM, Mar 2008]","start":29767369,"end":29770413,"strand":1,"description":"ubiquinol-cytochrome c reductase, complex III subunit X [Source:HGNC Symbol;Acc:HGNC:30863]"}, {"versioned_ensembl_gene_id":"ENSG00000172943.19","gene_symbol":"PHF8","gene_name":"PHD finger protein 8 [Source:HGNC Symbol;Acc:HGNC:20672]","synonyms":"ZNF422,KIAA1111,KDM7B,JHDM1F","biotype":"protein_coding","ncbi_id":"23133","summary":"The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":53936676,"end":54048958,"strand":-1,"description":"PHD finger protein 8 [Source:HGNC Symbol;Acc:HGNC:20672]"}, {"versioned_ensembl_gene_id":"ENSG00000232730.1","gene_symbol":"FAM8A4P","gene_name":"family with sequence similarity 8 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:16375]","synonyms":"FAM8A8P","biotype":"processed_pseudogene","ncbi_id":"386726","summary":null,"start":12321623,"end":12322835,"strand":1,"description":"family with sequence similarity 8 member A4, pseudogene [Source:HGNC Symbol;Acc:HGNC:16375]"}, {"versioned_ensembl_gene_id":"ENSG00000278674.1","gene_symbol":"ELOA3B","gene_name":"elongin A3 family member B [Source:HGNC Symbol;Acc:HGNC:31007]","synonyms":"TCEB3CL,HsT828","biotype":"protein_coding","ncbi_id":"728929","summary":null,"start":47022287,"end":47023927,"strand":-1,"description":"elongin A3 family member B [Source:HGNC Symbol;Acc:HGNC:31007]"}, {"versioned_ensembl_gene_id":"ENSG00000282270.1","gene_symbol":"PGBD4P1","gene_name":"piggyBac transposable element derived 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107161154","summary":null,"start":142763060,"end":142763466,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44066]"}, {"versioned_ensembl_gene_id":"ENSG00000275797.1","gene_symbol":"AC008746.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54446594,"end":54447473,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267587.1","gene_symbol":"AC090241.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46852632,"end":46853882,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266957.1","gene_symbol":"AC012254.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47077361,"end":47091280,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224060.3","gene_symbol":"ARSEP1","gene_name":"arylsulfatase E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:720]","synonyms":"ARSEP","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"10033","summary":null,"start":12339813,"end":12347495,"strand":1,"description":"arylsulfatase E pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:720]"}, {"versioned_ensembl_gene_id":"ENSG00000183791.4","gene_symbol":"ELOA3","gene_name":"elongin A3 [Source:HGNC Symbol;Acc:HGNC:24617]","synonyms":"TCEB3L2,TCEB3C,HsT829,ELOA3A","biotype":"protein_coding","ncbi_id":null,"summary":null,"start":47028202,"end":47030078,"strand":-1,"description":"elongin A3 [Source:HGNC Symbol;Acc:HGNC:24617]"}, {"versioned_ensembl_gene_id":"ENSG00000282628.1","gene_symbol":"TRBV29-1","gene_name":"T-cell receptor beta variable 29-1 [Source:HGNC Symbol;Acc:HGNC:12210]","synonyms":"TRBV291,TCRBV4S1A1T,TCRBV29S1","biotype":"TR_V_gene","ncbi_id":"28558","summary":null,"start":142780919,"end":142781607,"strand":1,"description":"T-cell receptor beta variable 29-1 [Source:HGNC Symbol;Acc:HGNC:12210]"}, {"versioned_ensembl_gene_id":"ENSG00000274744.1","gene_symbol":"ELOA3D","gene_name":"elongin A3 family member D [Source:HGNC Symbol;Acc:HGNC:33511]","synonyms":"TCEB3CL2","biotype":"protein_coding","ncbi_id":"100506888","summary":null,"start":46962768,"end":46964408,"strand":-1,"description":"elongin A3 family member D [Source:HGNC Symbol;Acc:HGNC:33511]"}, {"versioned_ensembl_gene_id":"ENSG00000279552.1","gene_symbol":"ZNF729","gene_name":"zinc finger protein 729 [Source:HGNC Symbol;Acc:HGNC:32464]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287226","summary":null,"start":22294615,"end":22294762,"strand":1,"description":"zinc finger protein 729 [Source:HGNC Symbol;Acc:HGNC:32464]"}, {"versioned_ensembl_gene_id":"ENSG00000254597.1","gene_symbol":"FAM90A10P","gene_name":"family with sequence similarity 90 member A10, pseudogene [Source:HGNC Symbol;Acc:HGNC:32258]","synonyms":"FAM90A10","biotype":"unprocessed_pseudogene","ncbi_id":"441328","summary":"FAM90A10 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]","start":7768977,"end":7771988,"strand":1,"description":"family with sequence similarity 90 member A10, pseudogene [Source:HGNC Symbol;Acc:HGNC:32258]"}, {"versioned_ensembl_gene_id":"ENSG00000279354.1","gene_symbol":"AC090373.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":46915021,"end":46915623,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128309.16","gene_symbol":"MPST","gene_name":"mercaptopyruvate sulfurtransferase [Source:HGNC Symbol;Acc:HGNC:7223]","synonyms":"TUM1,TST2,MST","biotype":"protein_coding","ncbi_id":"4357","summary":"This protein encoded by this gene catalyzes the transfer of a sulfur ion from 3-mercaptopyruvate to cyanide or other thiol compounds. It may be involved in cysteine degradation and cyanide detoxification. There is confusion in literature between this protein (mercaptopyruvate sulfurtransferase, MPST), which appears to be cytoplasmic, and thiosulfate sulfurtransferase (rhodanese, TST, GeneID:7263), which is a mitochondrial protein. Deficiency in MPST activity has been implicated in a rare inheritable disorder known as mercaptolactate-cysteine disulfiduria (MCDU). Alternatively spliced transcript variants encoding same or different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":37019635,"end":37029822,"strand":1,"description":"mercaptopyruvate sulfurtransferase [Source:HGNC Symbol;Acc:HGNC:7223]"}, {"versioned_ensembl_gene_id":"ENSG00000206181.5","gene_symbol":"ELOA2","gene_name":"elongin A2 [Source:HGNC Symbol;Acc:HGNC:30771]","synonyms":"TCEB3L,TCEB3B,HsT832","biotype":"protein_coding","ncbi_id":"51224","summary":"This gene encodes the transcriptionally active subunit of the SIII (or elongin) transcription elongation factor complex, which also includes two regulatory subunits, elongins B and C. This complex acts to increase the rate of RNA chain elongation by RNA polymerase II by suppressing transient pausing of the polymerase at many sites along the DNA template. Whereas a related protein with similar function, elongin A, is ubiquitously expressed, the encoded protein is specifically expressed in the testis, suggesting it may have a role in spermatogenesis. [provided by RefSeq, Jul 2008]","start":47032572,"end":47035621,"strand":-1,"description":"elongin A2 [Source:HGNC Symbol;Acc:HGNC:30771]"}, {"versioned_ensembl_gene_id":"ENSG00000272911.1","gene_symbol":"AC005696.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2688473,"end":2688960,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160785.13","gene_symbol":"SLC25A44","gene_name":"solute carrier family 25 member 44 [Source:HGNC Symbol;Acc:HGNC:29036]","synonyms":"KIAA0446,FLJ90431","biotype":"protein_coding","ncbi_id":"9673","summary":"SLC25A44 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]","start":156193932,"end":156212796,"strand":1,"description":"solute carrier family 25 member 44 [Source:HGNC Symbol;Acc:HGNC:29036]"}, {"versioned_ensembl_gene_id":"ENSG00000159339.13","gene_symbol":"PADI4","gene_name":"peptidyl arginine deiminase 4 [Source:HGNC Symbol;Acc:HGNC:18368]","synonyms":"PAD,PDI5,PDI4,PADI5","biotype":"protein_coding","ncbi_id":"23569","summary":"This gene is a member of a gene family which encodes enzymes responsible for the conversion of arginine residues to citrulline residues. This gene may play a role in granulocyte and macrophage development leading to inflammation and immune response. [provided by RefSeq, Jul 2008]","start":17308195,"end":17364004,"strand":1,"description":"peptidyl arginine deiminase 4 [Source:HGNC Symbol;Acc:HGNC:18368]"}, {"versioned_ensembl_gene_id":"ENSG00000272963.1","gene_symbol":"OR7A19P","gene_name":"olfactory receptor family 7 subfamily A member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15337]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"387853","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":46592573,"end":46593305,"strand":1,"description":"olfactory receptor family 7 subfamily A member 19 pseudogene [Source:HGNC Symbol;Acc:HGNC:15337]"}, {"versioned_ensembl_gene_id":"ENSG00000078043.15","gene_symbol":"PIAS2","gene_name":"protein inhibitor of activated STAT 2 [Source:HGNC Symbol;Acc:HGNC:17311]","synonyms":"ZMIZ4,PIASX-BETA,PIASX-ALPHA,miz","biotype":"protein_coding","ncbi_id":"9063","summary":"This gene encodes a member of the protein inhibitor of activated STAT family, which function as SUMO E3 ligases and play important roles in many cellular processes by mediating the sumoylation of target proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Isoforms of the encoded protein enhance the sumoylation of specific target proteins including the p53 tumor suppressor protein, c-Jun, and the androgen receptor. A pseudogene of this gene is located on the short arm of chromosome 4. The symbol MIZ1 has also been associated with ZBTB17 which is a different gene located on chromosome 1. [provided by RefSeq, Aug 2017]","start":46803224,"end":46920160,"strand":-1,"description":"protein inhibitor of activated STAT 2 [Source:HGNC Symbol;Acc:HGNC:17311]"}, {"versioned_ensembl_gene_id":"ENSG00000272369.1","gene_symbol":"AC008035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46537502,"end":46652550,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273574.1","gene_symbol":"LENG9","gene_name":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94059","summary":null,"start":54469723,"end":54471641,"strand":-1,"description":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]"}, {"versioned_ensembl_gene_id":"ENSG00000275481.1","gene_symbol":"AC025031.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46388856,"end":46392126,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248231.1","gene_symbol":"KRT8P4","gene_name":"keratin 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31057]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100509857","summary":null,"start":89412621,"end":89415071,"strand":-1,"description":"keratin 8 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:31057]"}, {"versioned_ensembl_gene_id":"ENSG00000187833.7","gene_symbol":"C2orf78","gene_name":"chromosome 2 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:34349]","synonyms":"hCG1989538,FLJ43987,COG5373","biotype":"protein_coding","ncbi_id":"388960","summary":null,"start":73784189,"end":73817147,"strand":1,"description":"chromosome 2 open reading frame 78 [Source:HGNC Symbol;Acc:HGNC:34349]"}, {"versioned_ensembl_gene_id":"ENSG00000276681.4","gene_symbol":"LENG8","gene_name":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]","synonyms":"pp13842,MGC40108,KIAA1932","biotype":"protein_coding","ncbi_id":"114823","summary":null,"start":54456812,"end":54469943,"strand":1,"description":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]"}, {"versioned_ensembl_gene_id":"ENSG00000109654.14","gene_symbol":"TRIM2","gene_name":"tripartite motif containing 2 [Source:HGNC Symbol;Acc:HGNC:15974]","synonyms":"RNF86,KIAA0517,CMT2R","biotype":"protein_coding","ncbi_id":"23321","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic filaments. It plays a neuroprotective role and functions as an E3-ubiquitin ligase in proteasome-mediated degradation of target proteins. Mutations in this gene can cause early-onset axonal neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]","start":153152342,"end":153339320,"strand":1,"description":"tripartite motif containing 2 [Source:HGNC Symbol;Acc:HGNC:15974]"}, {"versioned_ensembl_gene_id":"ENSG00000233750.3","gene_symbol":"CICP27","gene_name":"capicua transcriptional repressor pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:48835]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420257","summary":null,"start":131025,"end":134836,"strand":1,"description":"capicua transcriptional repressor pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:48835]"}, {"versioned_ensembl_gene_id":"ENSG00000273437.1","gene_symbol":"AC108673.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":129163606,"end":129163940,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224957.5","gene_symbol":"LINC01266","gene_name":"long intergenic non-protein coding RNA 1266 [Source:HGNC Symbol;Acc:HGNC:50309]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927215","summary":null,"start":536231,"end":846015,"strand":1,"description":"long intergenic non-protein coding RNA 1266 [Source:HGNC Symbol;Acc:HGNC:50309]"}, {"versioned_ensembl_gene_id":"ENSG00000226618.9","gene_symbol":"PRRC2A","gene_name":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]","synonyms":"D6S51E,BAT2,G2","biotype":"protein_coding","ncbi_id":"7916","summary":"A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]","start":31660168,"end":31677219,"strand":1,"description":"proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]"}, {"versioned_ensembl_gene_id":"ENSG00000228809.2","gene_symbol":"AL034428.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":16714844,"end":16730948,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133101.9","gene_symbol":"CCNA1","gene_name":"cyclin A1 [Source:HGNC Symbol;Acc:HGNC:1577]","synonyms":"CT146","biotype":"protein_coding","ncbi_id":"8900","summary":"The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. The cyclin encoded by this gene was shown to be expressed in testis and brain, as well as in several leukemic cell lines, and is thought to primarily function in the control of the germline meiotic cell cycle. This cyclin binds both CDK2 and CDC2 kinases, which give two distinct kinase activities, one appearing in S phase, the other in G2, and thus regulate separate functions in cell cycle. This cyclin was found to bind to important cell cycle regulators, such as Rb family proteins, transcription factor E2F-1, and the p21 family proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":36431520,"end":36442882,"strand":1,"description":"cyclin A1 [Source:HGNC Symbol;Acc:HGNC:1577]"}, {"versioned_ensembl_gene_id":"ENSG00000268020.3","gene_symbol":"AL627309.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":52473,"end":53312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240361.2","gene_symbol":"OR4G11P","gene_name":"olfactory receptor family 4 subfamily G member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:31276]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"403263","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":57598,"end":64116,"strand":1,"description":"olfactory receptor family 4 subfamily G member 11 pseudogene [Source:HGNC Symbol;Acc:HGNC:31276]"}, {"versioned_ensembl_gene_id":"ENSG00000188716.5","gene_symbol":"DUPD1","gene_name":"dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23481]","synonyms":"DUSP27","biotype":"protein_coding","ncbi_id":"338599","summary":null,"start":75037836,"end":75058514,"strand":-1,"description":"dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23481]"}, {"versioned_ensembl_gene_id":"ENSG00000183431.11","gene_symbol":"SF3A3","gene_name":"splicing factor 3a subunit 3 [Source:HGNC Symbol;Acc:HGNC:10767]","synonyms":"PRP9,SF3a60,SAP61,PRPF9","biotype":"protein_coding","ncbi_id":"10946","summary":"This gene encodes subunit 3 of the splicing factor 3a protein complex. The splicing factor 3a heterotrimer includes subunits 1, 2 and 3 and is necessary for the in vitro conversion of 15S U2 snRNP into an active 17S particle that performs pre-mRNA splicing. Subunit 3 interacts with subunit 1 through its amino-terminus while the zinc finger domain of subunit 3 plays a role in its binding to the 15S U2 snRNP. This gene has a pseudogene on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":37956975,"end":37990921,"strand":-1,"description":"splicing factor 3a subunit 3 [Source:HGNC Symbol;Acc:HGNC:10767]"}, {"versioned_ensembl_gene_id":"ENSG00000186092.5","gene_symbol":"OR4F5","gene_name":"olfactory receptor family 4 subfamily F member 5 [Source:HGNC Symbol;Acc:HGNC:14825]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79501","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":65419,"end":71585,"strand":1,"description":"olfactory receptor family 4 subfamily F member 5 [Source:HGNC Symbol;Acc:HGNC:14825]"}, {"versioned_ensembl_gene_id":"ENSG00000246985.7","gene_symbol":"SOCS2-AS1","gene_name":"SOCS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27054]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"144481","summary":null,"start":93542463,"end":93571768,"strand":-1,"description":"SOCS2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27054]"}, {"versioned_ensembl_gene_id":"ENSG00000241014.1","gene_symbol":"AC114490.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":34974356,"end":34985313,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237882.1","gene_symbol":"PPIAP13","gene_name":"peptidylprolyl isomerase A pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:9266]","synonyms":"PPIP3","biotype":"processed_pseudogene","ncbi_id":"5485","summary":null,"start":75089248,"end":75089725,"strand":-1,"description":"peptidylprolyl isomerase A pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:9266]"}, {"versioned_ensembl_gene_id":"ENSG00000239945.1","gene_symbol":"AL627309.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89551,"end":91105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238009.6","gene_symbol":"AL627309.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89295,"end":133723,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132964.11","gene_symbol":"CDK8","gene_name":"cyclin dependent kinase 8 [Source:HGNC Symbol;Acc:HGNC:1779]","synonyms":"K35","biotype":"protein_coding","ncbi_id":"1024","summary":"This gene encodes a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are known to be important regulators of cell cycle progression. This kinase and its regulatory subunit, cyclin C, are components of the Mediator transcriptional regulatory complex, involved in both transcriptional activation and repression by phosphorylation of the carboxy-terminal domain of the largest subunit of RNA polymerase II. This kinase regulates transcription by targeting the cyclin-dependent kinase 7 subunits of the general transcription initiation factor IIH, thus providing a link between the Mediator complex and the basal transcription machinery. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":26254104,"end":26405238,"strand":1,"description":"cyclin dependent kinase 8 [Source:HGNC Symbol;Acc:HGNC:1779]"}, {"versioned_ensembl_gene_id":"ENSG00000243749.1","gene_symbol":"TMEM35B","gene_name":"transmembrane protein 35B [Source:HGNC Symbol;Acc:HGNC:40021]","synonyms":"ZMYM6NB","biotype":"protein_coding","ncbi_id":"100506144","summary":null,"start":34981535,"end":34985353,"strand":-1,"description":"transmembrane protein 35B [Source:HGNC Symbol;Acc:HGNC:40021]"}, {"versioned_ensembl_gene_id":"ENSG00000279984.1","gene_symbol":"BNIP3P31","gene_name":"BCL2 interacting protein 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49711]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480282","summary":null,"start":22307184,"end":22308075,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:49711]"}, {"versioned_ensembl_gene_id":"ENSG00000279731.1","gene_symbol":"AC073539.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22267900,"end":22269542,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279902.1","gene_symbol":"AC073539.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22251461,"end":22253554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238075.1","gene_symbol":"RPSAP32","gene_name":"ribosomal protein SA pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:50310]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"402123","summary":null,"start":617789,"end":618314,"strand":-1,"description":"ribosomal protein SA pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:50310]"}, {"versioned_ensembl_gene_id":"ENSG00000224239.1","gene_symbol":"AC090044.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":857124,"end":858091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271741.1","gene_symbol":"AC114490.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":34981533,"end":35031741,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251609.2","gene_symbol":"SETP12","gene_name":"SET pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42931]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419158","summary":null,"start":120895494,"end":120897083,"strand":-1,"description":"SET pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42931]"}, {"versioned_ensembl_gene_id":"ENSG00000276219.4","gene_symbol":"ZNF676","gene_name":"zinc finger protein 676 [Source:HGNC Symbol;Acc:HGNC:20429]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163223","summary":null,"start":22179091,"end":22215686,"strand":-1,"description":"zinc finger protein 676 [Source:HGNC Symbol;Acc:HGNC:20429]"}, {"versioned_ensembl_gene_id":"ENSG00000268903.1","gene_symbol":"AL627309.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135141,"end":135895,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235158.1","gene_symbol":"AC087430.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1008135,"end":1012934,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240521.1","gene_symbol":"AC092979.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":148850933,"end":148960112,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250198.1","gene_symbol":"LINC02199","gene_name":"long intergenic non-protein coding RNA 2199 [Source:HGNC Symbol;Acc:HGNC:53065]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929284","summary":null,"start":8839732,"end":8881525,"strand":1,"description":"long intergenic non-protein coding RNA 2199 [Source:HGNC Symbol;Acc:HGNC:53065]"}, {"versioned_ensembl_gene_id":"ENSG00000269981.1","gene_symbol":"AL627309.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137682,"end":137965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244089.1","gene_symbol":"HMGB1P30","gene_name":"high mobility group box 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39121]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873893","summary":null,"start":148824782,"end":148825387,"strand":-1,"description":"high mobility group box 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39121]"}, {"versioned_ensembl_gene_id":"ENSG00000239906.1","gene_symbol":"AL627309.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139790,"end":140339,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271052.1","gene_symbol":"AC108738.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":161222911,"end":161223147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233183.2","gene_symbol":"AL138889.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33893323,"end":33927631,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226447.1","gene_symbol":"AL117337.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":37976825,"end":37992467,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235508.3","gene_symbol":"RPS2P7","gene_name":"ribosomal protein S2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:15838]","synonyms":"RPS2L1,dJ688G8.1","biotype":"processed_pseudogene","ncbi_id":"86781","summary":null,"start":45640486,"end":45641370,"strand":-1,"description":"ribosomal protein S2 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:15838]"}, {"versioned_ensembl_gene_id":"ENSG00000092445.11","gene_symbol":"TYRO3","gene_name":"TYRO3 protein tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12446]","synonyms":"Tif,Sky,RSE,Rek,Etk-2,Dtk,Brt","biotype":"protein_coding","ncbi_id":"7301","summary":"The gene is part of a 3-member transmembrane receptor kinase receptor family with a processed pseudogene distal on chromosome 15. The encoded protein is activated by the products of the growth arrest-specific gene 6 and protein S genes and is involved in controlling cell survival and proliferation, spermatogenesis, immunoregulation and phagocytosis. The encoded protein has also been identified as a cell entry factor for Ebola and Marburg viruses. [provided by RefSeq, May 2010]","start":41557675,"end":41583586,"strand":1,"description":"TYRO3 protein tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:12446]"}, {"versioned_ensembl_gene_id":"ENSG00000241860.6","gene_symbol":"AL627309.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":141474,"end":173862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223612.3","gene_symbol":"AC241585.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145233001,"end":145233519,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279554.1","gene_symbol":"AC130448.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24208105,"end":24208478,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279276.1","gene_symbol":"AC130454.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":23962951,"end":23963351,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279350.1","gene_symbol":"BNIP3P30","gene_name":"BCL2 interacting protein 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49710]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481694","summary":null,"start":22203120,"end":22203995,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:49710]"}, {"versioned_ensembl_gene_id":"ENSG00000256374.2","gene_symbol":"PPIAL4D","gene_name":"peptidylprolyl isomerase A like 4D [Source:HGNC Symbol;Acc:HGNC:33998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645142","summary":null,"start":145241630,"end":145242124,"strand":-1,"description":"peptidylprolyl isomerase A like 4D [Source:HGNC Symbol;Acc:HGNC:33998]"}, {"versioned_ensembl_gene_id":"ENSG00000225394.1","gene_symbol":"AC106883.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":194454581,"end":194455142,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279326.1","gene_symbol":"AC004972.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":80972516,"end":80974724,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230173.1","gene_symbol":"LINC01790","gene_name":"long intergenic non-protein coding RNA 1790 [Source:HGNC Symbol;Acc:HGNC:52579]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927431","summary":null,"start":194730595,"end":194761435,"strand":1,"description":"long intergenic non-protein coding RNA 1790 [Source:HGNC Symbol;Acc:HGNC:52579]"}, {"versioned_ensembl_gene_id":"ENSG00000166501.12","gene_symbol":"PRKCB","gene_name":"protein kinase C beta [Source:HGNC Symbol;Acc:HGNC:9395]","synonyms":"PRKCB2,PRKCB1,PKCB","biotype":"protein_coding","ncbi_id":"5579","summary":"Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase has been reported to be involved in many different cellular functions, such as B cell activation, apoptosis induction, endothelial cell proliferation, and intestinal sugar absorption. Studies in mice also suggest that this kinase may also regulate neuronal functions and correlate fear-induced conflict behavior after stress. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]","start":23836001,"end":24220611,"strand":1,"description":"protein kinase C beta [Source:HGNC Symbol;Acc:HGNC:9395]"}, {"versioned_ensembl_gene_id":"ENSG00000249346.6","gene_symbol":"LINC01016","gene_name":"long intergenic non-protein coding RNA 1016 [Source:HGNC Symbol;Acc:HGNC:48991]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507584","summary":null,"start":33867506,"end":33896914,"strand":-1,"description":"long intergenic non-protein coding RNA 1016 [Source:HGNC Symbol;Acc:HGNC:48991]"}, {"versioned_ensembl_gene_id":"ENSG00000102178.12","gene_symbol":"UBL4A","gene_name":"ubiquitin like 4A [Source:HGNC Symbol;Acc:HGNC:12505]","synonyms":"UBL4,TMA24,MDY2,GET5,GDX,DXS254E","biotype":"protein_coding","ncbi_id":"8266","summary":null,"start":154483717,"end":154486670,"strand":-1,"description":"ubiquitin like 4A [Source:HGNC Symbol;Acc:HGNC:12505]"}, {"versioned_ensembl_gene_id":"ENSG00000241599.1","gene_symbol":"AL627309.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":160446,"end":161525,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226671.1","gene_symbol":"AC005008.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81191398,"end":81192009,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237896.6","gene_symbol":"AC005008.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":81175508,"end":81199115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180083.10","gene_symbol":"WFDC11","gene_name":"WAP four-disulfide core domain 11 [Source:HGNC Symbol;Acc:HGNC:20478]","synonyms":"WAP11","biotype":"protein_coding","ncbi_id":"259239","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008]","start":45648563,"end":45670270,"strand":-1,"description":"WAP four-disulfide core domain 11 [Source:HGNC Symbol;Acc:HGNC:20478]"}, {"versioned_ensembl_gene_id":"ENSG00000279928.2","gene_symbol":"FO538757.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":182696,"end":184174,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177156.10","gene_symbol":"TALDO1","gene_name":"transaldolase 1 [Source:HGNC Symbol;Acc:HGNC:11559]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6888","summary":"Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis. [provided by RefSeq, Jul 2008]","start":747329,"end":765024,"strand":1,"description":"transaldolase 1 [Source:HGNC Symbol;Acc:HGNC:11559]"}, {"versioned_ensembl_gene_id":"ENSG00000262352.1","gene_symbol":"LINC02564","gene_name":"long intergenic non-protein coding RNA 2564 [Source:HGNC Symbol;Acc:HGNC:53604]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11103,"end":15928,"strand":1,"description":"long intergenic non-protein coding RNA 2564 [Source:HGNC Symbol;Acc:HGNC:53604]"}, {"versioned_ensembl_gene_id":"ENSG00000226722.3","gene_symbol":"LINC00424","gene_name":"long intergenic non-protein coding RNA 424 [Source:HGNC Symbol;Acc:HGNC:42815]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874182","summary":null,"start":21872770,"end":21878160,"strand":-1,"description":"long intergenic non-protein coding RNA 424 [Source:HGNC Symbol;Acc:HGNC:42815]"}, {"versioned_ensembl_gene_id":"ENSG00000263305.1","gene_symbol":"AP005530.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14195,"end":16898,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259187.1","gene_symbol":"AC122108.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44826540,"end":44827094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259479.6","gene_symbol":"SORD2P","gene_name":"sorbitol dehydrogenase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49919]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"653381","summary":null,"start":44825747,"end":44884694,"strand":-1,"description":"sorbitol dehydrogenase 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:49919]"}, {"versioned_ensembl_gene_id":"ENSG00000271362.1","gene_symbol":"AL138889.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33883170,"end":33883411,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223514.1","gene_symbol":"AC004866.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":81335106,"end":81335183,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224134.1","gene_symbol":"AC004866.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":81431731,"end":81432796,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224692.1","gene_symbol":"Z68694.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103258572,"end":103259581,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000006611.15","gene_symbol":"USH1C","gene_name":"USH1 protein network component harmonin [Source:HGNC Symbol;Acc:HGNC:12597]","synonyms":"PDZD7C,PDZ73,PDZ-73,NY-CO-38,NY-CO-37,harmonin,DFNB18,AIE-75","biotype":"protein_coding","ncbi_id":"10083","summary":"This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]","start":17493895,"end":17544416,"strand":-1,"description":"USH1 protein network component harmonin [Source:HGNC Symbol;Acc:HGNC:12597]"}, {"versioned_ensembl_gene_id":"ENSG00000179855.5","gene_symbol":"GIPC3","gene_name":"GIPC PDZ domain containing family member 3 [Source:HGNC Symbol;Acc:HGNC:18183]","synonyms":"DFNB95,DFNB72,DFNB15,C19orf64","biotype":"protein_coding","ncbi_id":"126326","summary":"The protein encoded by this gene belongs to the GIPC family. Studies in mice suggest that this gene is required for postnatal maturation of the hair bundle and long-term survival of hair cells and spiral ganglion in the ear. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2011]","start":3585553,"end":3593541,"strand":1,"description":"GIPC PDZ domain containing family member 3 [Source:HGNC Symbol;Acc:HGNC:18183]"}, {"versioned_ensembl_gene_id":"ENSG00000232968.1","gene_symbol":"EIF4EP4","gene_name":"eukaryotic translation initiation factor 4E pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51462]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421455","summary":null,"start":81463036,"end":81463613,"strand":-1,"description":"eukaryotic translation initiation factor 4E pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:51462]"}, {"versioned_ensembl_gene_id":"ENSG00000279457.4","gene_symbol":"FO538757.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":185217,"end":195411,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128408.8","gene_symbol":"RIBC2","gene_name":"RIB43A domain with coiled-coils 2 [Source:HGNC Symbol;Acc:HGNC:13241]","synonyms":"FLJ25720,DKFZp566F0546,C22orf11","biotype":"protein_coding","ncbi_id":"26150","summary":null,"start":45413691,"end":45432496,"strand":1,"description":"RIB43A domain with coiled-coils 2 [Source:HGNC Symbol;Acc:HGNC:13241]"}, {"versioned_ensembl_gene_id":"ENSG00000271291.1","gene_symbol":"AC245014.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":145269604,"end":145269890,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276216.1","gene_symbol":"AC245014.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145281116,"end":145281462,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236140.1","gene_symbol":"AC245014.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":145286610,"end":145287755,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229893.2","gene_symbol":"AC005091.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27733064,"end":27740395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000153814.11","gene_symbol":"JAZF1","gene_name":"JAZF zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:28917]","synonyms":"ZNF802,TIP27,DKFZp761K2222","biotype":"protein_coding","ncbi_id":"221895","summary":"This gene encodes a nuclear protein with three C2H2-type zinc fingers, and functions as a transcriptional repressor. Chromosomal aberrations involving this gene are associated with endometrial stromal tumors. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized [provided by RefSeq, Jul 2008]","start":27830573,"end":28180743,"strand":-1,"description":"JAZF zinc finger 1 [Source:HGNC Symbol;Acc:HGNC:28917]"}, {"versioned_ensembl_gene_id":"ENSG00000065609.14","gene_symbol":"SNAP91","gene_name":"synaptosome associated protein 91 [Source:HGNC Symbol;Acc:HGNC:14986]","synonyms":"KIAA0656,CALM,AP180","biotype":"protein_coding","ncbi_id":"9892","summary":null,"start":83552880,"end":83709691,"strand":-1,"description":"synaptosome associated protein 91 [Source:HGNC Symbol;Acc:HGNC:14986]"}, {"versioned_ensembl_gene_id":"ENSG00000259742.1","gene_symbol":"AC090888.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":44914802,"end":44930622,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168634.4","gene_symbol":"WFDC13","gene_name":"WAP four-disulfide core domain 13 [Source:HGNC Symbol;Acc:HGNC:16131]","synonyms":"WAP13,dJ601O1.3,C20orf138","biotype":"protein_coding","ncbi_id":"164237","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008]","start":45702016,"end":45708817,"strand":1,"description":"WAP four-disulfide core domain 13 [Source:HGNC Symbol;Acc:HGNC:16131]"}, {"versioned_ensembl_gene_id":"ENSG00000259231.2","gene_symbol":"AC090888.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44919376,"end":44920820,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182931.9","gene_symbol":"WFDC10B","gene_name":"WAP four-disulfide core domain 10B [Source:HGNC Symbol;Acc:HGNC:20479]","synonyms":"WAP12","biotype":"protein_coding","ncbi_id":"280664","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Two alternatively spliced transcript variants have been found for this gene, and they encode distinct isoforms. [provided by RefSeq, Jul 2008]","start":45684653,"end":45705019,"strand":-1,"description":"WAP four-disulfide core domain 10B [Source:HGNC Symbol;Acc:HGNC:20479]"}, {"versioned_ensembl_gene_id":"ENSG00000006638.11","gene_symbol":"TBXA2R","gene_name":"thromboxane A2 receptor [Source:HGNC Symbol;Acc:HGNC:11608]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6915","summary":"This gene encodes a member of the G protein-coupled receptor family. The protein interacts with thromboxane A2 to induce platelet aggregation and regulate hemostasis. A mutation in this gene results in a bleeding disorder. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":3594506,"end":3606840,"strand":-1,"description":"thromboxane A2 receptor [Source:HGNC Symbol;Acc:HGNC:11608]"}, {"versioned_ensembl_gene_id":"ENSG00000276476.2","gene_symbol":"LINC00540","gene_name":"long intergenic non-protein coding RNA 540 [Source:NCBI gene;Acc:100506622]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506622","summary":null,"start":22040975,"end":22276524,"strand":1,"description":"long intergenic non-protein coding RNA 540 [Source:NCBI gene;Acc:100506622]"}, {"versioned_ensembl_gene_id":"ENSG00000125107.17","gene_symbol":"CNOT1","gene_name":"CCR4-NOT transcription complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:7877]","synonyms":"NOT1H,NOT1,KIAA1007,CDC39,AD-005","biotype":"protein_coding","ncbi_id":"23019","summary":null,"start":58519951,"end":58629886,"strand":-1,"description":"CCR4-NOT transcription complex subunit 1 [Source:HGNC Symbol;Acc:HGNC:7877]"}, {"versioned_ensembl_gene_id":"ENSG00000275470.4","gene_symbol":"LENG8-AS1","gene_name":"LENG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40705]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"104355426","summary":null,"start":54452738,"end":54456970,"strand":-1,"description":"LENG8 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40705]"}, {"versioned_ensembl_gene_id":"ENSG00000237175.1","gene_symbol":"NME1P1","gene_name":"NME/NM23 nucleoside diphosphate kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39904]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874501","summary":null,"start":22099163,"end":22099544,"strand":-1,"description":"NME/NM23 nucleoside diphosphate kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39904]"}, {"versioned_ensembl_gene_id":"ENSG00000226118.1","gene_symbol":"MTND3P1","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39856]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873208","summary":null,"start":22113119,"end":22113338,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39856]"}, {"versioned_ensembl_gene_id":"ENSG00000070501.11","gene_symbol":"POLB","gene_name":"DNA polymerase beta [Source:HGNC Symbol;Acc:HGNC:9174]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5423","summary":"The protein encoded by this gene is a DNA polymerase involved in base excision and repair, also called gap-filling DNA synthesis. The encoded protein, acting as a monomer, is normally found in the cytoplasm, but it translocates to the nucleus upon DNA damage. Several transcript variants of this gene exist, but the full-length nature of only one has been described to date. [provided by RefSeq, Sep 2011]","start":42338454,"end":42371808,"strand":1,"description":"DNA polymerase beta [Source:HGNC Symbol;Acc:HGNC:9174]"}, {"versioned_ensembl_gene_id":"ENSG00000234545.7","gene_symbol":"FAM133B","gene_name":"family with sequence similarity 133 member B [Source:HGNC Symbol;Acc:HGNC:28629]","synonyms":"MGC40405","biotype":"protein_coding","ncbi_id":"257415","summary":null,"start":92560793,"end":92590394,"strand":-1,"description":"family with sequence similarity 133 member B [Source:HGNC Symbol;Acc:HGNC:28629]"}, {"versioned_ensembl_gene_id":"ENSG00000225117.1","gene_symbol":"ARSDP1","gene_name":"arylsulfatase D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:718]","synonyms":"ARSDY1,ARSDP","biotype":"unprocessed_pseudogene","ncbi_id":"10034","summary":null,"start":12354096,"end":12387328,"strand":1,"description":"arylsulfatase D pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:718]"}, {"versioned_ensembl_gene_id":"ENSG00000206159.10","gene_symbol":"GYG2P1","gene_name":"glycogenin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4701]","synonyms":"GYG2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"352887","summary":null,"start":12354416,"end":12420456,"strand":-1,"description":"glycogenin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4701]"}, {"versioned_ensembl_gene_id":"ENSG00000176731.11","gene_symbol":"C8orf59","gene_name":"chromosome 8 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:32235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401466","summary":null,"start":85214076,"end":85220421,"strand":-1,"description":"chromosome 8 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:32235]"}, {"versioned_ensembl_gene_id":"ENSG00000204065.2","gene_symbol":"TCEAL5","gene_name":"transcription elongation factor A like 5 [Source:HGNC Symbol;Acc:HGNC:22282]","synonyms":"WEX4","biotype":"protein_coding","ncbi_id":"340543","summary":"This gene, which is located on the X chromosome, encodes a protein which contains a BEX (brain expressed X-liked like family) domain. This domain is found in proteins encoded by the TCEAL elongation factor (transcription elongation factor A (SII)-like) gene family also located on the X chromosome. The coding region for this gene is located entirely in the terminal exon. [provided by RefSeq, Sep 2011]","start":103273691,"end":103276872,"strand":-1,"description":"transcription elongation factor A like 5 [Source:HGNC Symbol;Acc:HGNC:22282]"}, {"versioned_ensembl_gene_id":"ENSG00000279819.1","gene_symbol":"AL390318.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":22693953,"end":22694639,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000150867.13","gene_symbol":"PIP4K2A","gene_name":"phosphatidylinositol-5-phosphate 4-kinase type 2 alpha [Source:HGNC Symbol;Acc:HGNC:8997]","synonyms":"PIP5KIIA,PIP5K2A,PIP5KIIalpha","biotype":"protein_coding","ncbi_id":"5305","summary":"Phosphatidylinositol-5,4-bisphosphate, the precursor to second messengers of the phosphoinositide signal transduction pathways, is thought to be involved in the regulation of secretion, cell proliferation, differentiation, and motility. The protein encoded by this gene is one of a family of enzymes capable of catalyzing the phosphorylation of phosphatidylinositol-5-phosphate on the fourth hydroxyl of the myo-inositol ring to form phosphatidylinositol-5,4-bisphosphate. The amino acid sequence of this enzyme does not show homology to other kinases, but the recombinant protein does exhibit kinase activity. This gene is a member of the phosphatidylinositol-5-phosphate 4-kinase family. [provided by RefSeq, Jul 2008]","start":22534849,"end":22714555,"strand":-1,"description":"phosphatidylinositol-5-phosphate 4-kinase type 2 alpha [Source:HGNC Symbol;Acc:HGNC:8997]"}, {"versioned_ensembl_gene_id":"ENSG00000143727.15","gene_symbol":"ACP1","gene_name":"acid phosphatase 1, soluble [Source:HGNC Symbol;Acc:HGNC:122]","synonyms":"LMWPTP,LMW-PTP,HAAP","biotype":"protein_coding","ncbi_id":"52","summary":"The product of this gene belongs to the phosphotyrosine protein phosphatase family of proteins. It functions as an acid phosphatase and a protein tyrosine phosphatase by hydrolyzing protein tyrosine phosphate to protein tyrosine and orthophosphate. This enzyme also hydrolyzes orthophosphoric monoesters to alcohol and orthophosphate. This gene is genetically polymorphic, and three common alleles segregating at the corresponding locus give rise to six phenotypes. Each allele appears to encode at least two electrophoretically different isozymes, Bf and Bs, which are produced in allele-specific ratios. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Aug 2008]","start":264140,"end":278283,"strand":1,"description":"acid phosphatase 1, soluble [Source:HGNC Symbol;Acc:HGNC:122]"}, {"versioned_ensembl_gene_id":"ENSG00000275553.3","gene_symbol":"ELOA3C","gene_name":"elongin A3 family member C [Source:HGNC Symbol;Acc:HGNC:52410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"107983955","summary":null,"start":46968695,"end":46969912,"strand":-1,"description":"elongin A3 family member C [Source:HGNC Symbol;Acc:HGNC:52410]"}, {"versioned_ensembl_gene_id":"ENSG00000249741.2","gene_symbol":"AC093890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143911514,"end":143912053,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164161.9","gene_symbol":"HHIP","gene_name":"hedgehog interacting protein [Source:HGNC Symbol;Acc:HGNC:14866]","synonyms":"HIP,FLJ20992","biotype":"protein_coding","ncbi_id":"64399","summary":"This gene encodes a member of the hedgehog-interacting protein (HHIP) family. The hedgehog (HH) proteins are evolutionarily conserved protein, which are important morphogens for a wide range of developmental processes, including anteroposterior patterns of limbs and regulation of left-right asymmetry in embryonic development. Multiple cell-surface receptors are responsible for transducing and/or regulating HH signals. The HHIP encoded by this gene is a highly conserved, vertebrate-specific inhibitor of HH signaling. It interacts with all three HH family members, SHH, IHH and DHH. Two single nucleotide polymorphisms (SNPs) near this gene are significantly associated with risk of chronic obstructive pulmonary disease (COPD). A single nucleotide polymorphism in this gene is also strongly associated with human height.[provided by RefSeq, Feb 2011]","start":144646021,"end":144745271,"strand":1,"description":"hedgehog interacting protein [Source:HGNC Symbol;Acc:HGNC:14866]"}, {"versioned_ensembl_gene_id":"ENSG00000231725.1","gene_symbol":"VN1R110P","gene_name":"vomeronasal 1 receptor 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:37438]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100312803","summary":null,"start":48636165,"end":48637135,"strand":1,"description":"vomeronasal 1 receptor 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:37438]"}, {"versioned_ensembl_gene_id":"ENSG00000232363.1","gene_symbol":"AL021391.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45435864,"end":45448743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255097.1","gene_symbol":"AP006259.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9242448,"end":9245509,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255378.1","gene_symbol":"PRR23D2","gene_name":"proline rich 23 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:49396]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100133251","summary":null,"start":7778591,"end":7781413,"strand":-1,"description":"proline rich 23 domain containing 2 [Source:HGNC Symbol;Acc:HGNC:49396]"}, {"versioned_ensembl_gene_id":"ENSG00000213406.3","gene_symbol":"ANXA2P1","gene_name":"annexin A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:538]","synonyms":"LPC2A,ANX2P1,ANX2L1","biotype":"processed_pseudogene","ncbi_id":"303","summary":null,"start":153307792,"end":153308717,"strand":-1,"description":"annexin A2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:538]"}, {"versioned_ensembl_gene_id":"ENSG00000184014.7","gene_symbol":"DENND5A","gene_name":"DENN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:19344]","synonyms":"FLJ43455,FLJ33829,FLJ22354,RAB6IP1,KIAA1091","biotype":"protein_coding","ncbi_id":"23258","summary":"This gene encodes a DENN-domain-containing protein that functions as a RAB-activating guanine nucleotide exchange factor (GEF). This protein catalyzes the conversion of GDP to GTP and thereby converts inactive GDP-bound Rab proteins into their active GTP-bound form. The encoded protein is recruited by RAB6 onto Golgi membranes and is therefore referred to as RAB6-interacting protein 1. This protein binds with RAB39 as well. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene are associated with early infantile epileptic encephalopathy-49. [provided by RefSeq, Feb 2017]","start":9138825,"end":9265390,"strand":-1,"description":"DENN domain containing 5A [Source:HGNC Symbol;Acc:HGNC:19344]"}, {"versioned_ensembl_gene_id":"ENSG00000235806.1","gene_symbol":"AF241728.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38770331,"end":38799658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230196.1","gene_symbol":"DDX43P3","gene_name":"DEAD-box helicase 43 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50782]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481709","summary":null,"start":81610884,"end":81611326,"strand":-1,"description":"DEAD-box helicase 43 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:50782]"}, {"versioned_ensembl_gene_id":"ENSG00000251237.1","gene_symbol":"B3GNTL1P1","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51317]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481968","summary":null,"start":52889666,"end":52889954,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51317]"}, {"versioned_ensembl_gene_id":"ENSG00000233491.7","gene_symbol":"AC008163.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":81489204,"end":81691406,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280210.1","gene_symbol":"VN1R85P","gene_name":"vomeronasal 1 receptor 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:37405]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312830","summary":null,"start":22174766,"end":22175191,"strand":-1,"description":"vomeronasal 1 receptor 85 pseudogene [Source:HGNC Symbol;Acc:HGNC:37405]"}, {"versioned_ensembl_gene_id":"ENSG00000284735.1","gene_symbol":"AL139424.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10381906,"end":10387150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248898.1","gene_symbol":"AC022126.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52675193,"end":52788026,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234162.1","gene_symbol":"AC009505.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":105959084,"end":105962006,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213199.7","gene_symbol":"ASIC3","gene_name":"acid sensing ion channel subunit 3 [Source:HGNC Symbol;Acc:HGNC:101]","synonyms":"DRASIC,ACCN3,TNaC1","biotype":"protein_coding","ncbi_id":"9311","summary":"This gene encodes a member of the degenerin/epithelial sodium channel (DEG/ENaC) superfamily. The members of this family are amiloride-sensitive sodium channels that contain intracellular N and C termini, two hydrophobic transmembrane regions, and a large extracellular loop, which has many cysteine residues with conserved spacing. The member encoded by this gene is an acid sensor and may play an important role in the detection of lasting pH changes. In addition, a heteromeric association between this member and acid-sensing (proton-gated) ion channel 2 has been observed as proton-gated channels sensitive to gadolinium. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]","start":151048292,"end":151052756,"strand":1,"description":"acid sensing ion channel subunit 3 [Source:HGNC Symbol;Acc:HGNC:101]"}, {"versioned_ensembl_gene_id":"ENSG00000279661.1","gene_symbol":"MTDHP5","gene_name":"metadherin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418836","summary":null,"start":22140532,"end":22141117,"strand":1,"description":"metadherin pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52361]"}, {"versioned_ensembl_gene_id":"ENSG00000254776.1","gene_symbol":"AC084121.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7793716,"end":7795870,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249899.5","gene_symbol":"AC025180.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":52932419,"end":52990278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275641.1","gene_symbol":"PCGF7P","gene_name":"polycomb group ring finger 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:30341]","synonyms":"RNF134P1","biotype":"processed_pseudogene","ncbi_id":"253272","summary":null,"start":22137931,"end":22138981,"strand":1,"description":"polycomb group ring finger 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:30341]"}, {"versioned_ensembl_gene_id":"ENSG00000279577.1","gene_symbol":"AC073539.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22130325,"end":22130489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282733.1","gene_symbol":"AC243659.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":46419950,"end":46533777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165175.15","gene_symbol":"MID1IP1","gene_name":"MID1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20715]","synonyms":"FLJ10386,THRSPL,STRAIT11499,MIG12,G12-like","biotype":"protein_coding","ncbi_id":"58526","summary":null,"start":38801432,"end":38806537,"strand":1,"description":"MID1 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:20715]"}, {"versioned_ensembl_gene_id":"ENSG00000258304.1","gene_symbol":"AC233290.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76115711,"end":76116100,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269711.1","gene_symbol":"AC008763.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7678501,"end":7682854,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276262.2","gene_symbol":"NSF","gene_name":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]","synonyms":"SKD2,SEC18","biotype":"protein_coding","ncbi_id":"4905","summary":null,"start":46419843,"end":46586373,"strand":1,"description":"N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:HGNC Symbol;Acc:HGNC:8016]"}, {"versioned_ensembl_gene_id":"ENSG00000152684.10","gene_symbol":"PELO","gene_name":"pelota mRNA surveillance and ribosome rescue factor [Source:HGNC Symbol;Acc:HGNC:8829]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53918","summary":"This gene encodes a protein which contains a conserved nuclear localization signal. The encoded protein may have a role in spermatogenesis, cell cycle control, and in meiotic cell division. [provided by RefSeq, Jul 2008]","start":52787940,"end":52804046,"strand":1,"description":"pelota mRNA surveillance and ribosome rescue factor [Source:HGNC Symbol;Acc:HGNC:8829]"}, {"versioned_ensembl_gene_id":"ENSG00000183019.7","gene_symbol":"MCEMP1","gene_name":"mast cell expressed membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:27291]","synonyms":"MGC132456,C19orf59","biotype":"protein_coding","ncbi_id":"199675","summary":"This gene encodes a single-pass transmembrane protein. Based on its expression pattern, it is speculated to be involved in regulating mast cell differentiation or immune responses. [provided by RefSeq, Jul 2008]","start":7676628,"end":7679826,"strand":1,"description":"mast cell expressed membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:27291]"}, {"versioned_ensembl_gene_id":"ENSG00000257872.1","gene_symbol":"AC233290.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":76137425,"end":76138610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274247.4","gene_symbol":"PRSS1","gene_name":"protease, serine 1 [Source:HGNC Symbol;Acc:HGNC:9475]","synonyms":"TRY1","biotype":"protein_coding","ncbi_id":"5644","summary":"This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is secreted by the pancreas and cleaved to its active form in the small intestine. It is active on peptide linkages involving the carboxyl group of lysine or arginine. Mutations in this gene are associated with hereditary pancreatitis. This gene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. [provided by RefSeq, Jul 2008]","start":142790185,"end":142793793,"strand":1,"description":"protease, serine 1 [Source:HGNC Symbol;Acc:HGNC:9475]"}, {"versioned_ensembl_gene_id":"ENSG00000274875.1","gene_symbol":"ZNF92P2","gene_name":"zinc finger protein 92 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419705","summary":null,"start":22128748,"end":22130323,"strand":-1,"description":"zinc finger protein 92 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39554]"}, {"versioned_ensembl_gene_id":"ENSG00000274064.1","gene_symbol":"AC040978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140039756,"end":140041037,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250733.5","gene_symbol":"C8orf17","gene_name":"chromosome 8 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:17737]","synonyms":"MOST-1","biotype":"TEC","ncbi_id":"100507249","summary":null,"start":139931172,"end":139933946,"strand":1,"description":"chromosome 8 open reading frame 17 [Source:HGNC Symbol;Acc:HGNC:17737]"}, {"versioned_ensembl_gene_id":"ENSG00000253574.5","gene_symbol":"AC021744.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":139911238,"end":139916620,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275216.1","gene_symbol":"AL161431.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109269634,"end":109273838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282164.2","gene_symbol":"PEG13","gene_name":"paternally expressed 13 [Source:HGNC Symbol;Acc:HGNC:19969]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"359809","summary":null,"start":140094894,"end":140100560,"strand":-1,"description":"paternally expressed 13 [Source:HGNC Symbol;Acc:HGNC:19969]"}, {"versioned_ensembl_gene_id":"ENSG00000238123.1","gene_symbol":"MID1IP1-AS1","gene_name":"MID1IP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40932]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874211","summary":null,"start":38801568,"end":38803883,"strand":-1,"description":"MID1IP1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40932]"}, {"versioned_ensembl_gene_id":"ENSG00000169714.16","gene_symbol":"CNBP","gene_name":"CCHC-type zinc finger nucleic acid binding protein [Source:HGNC Symbol;Acc:HGNC:13164]","synonyms":"ZNF9,ZCCHC22,RNF163,DM2,CNBP1","biotype":"protein_coding","ncbi_id":"7555","summary":"This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016]","start":129169484,"end":129183922,"strand":-1,"description":"CCHC-type zinc finger nucleic acid binding protein [Source:HGNC Symbol;Acc:HGNC:13164]"}, {"versioned_ensembl_gene_id":"ENSG00000272123.1","gene_symbol":"AC008966.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53089016,"end":53089468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226641.1","gene_symbol":"AL391647.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41322601,"end":41323111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284642.1","gene_symbol":"AL139424.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10395416,"end":10397432,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267795.5","gene_symbol":"SMIM22","gene_name":"small integral membrane protein 22 [Source:HGNC Symbol;Acc:HGNC:48329]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440335","summary":null,"start":4788397,"end":4796491,"strand":1,"description":"small integral membrane protein 22 [Source:HGNC Symbol;Acc:HGNC:48329]"}, {"versioned_ensembl_gene_id":"ENSG00000243265.1","gene_symbol":"RPL23AP55","gene_name":"ribosomal protein L23a pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:35997]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271467","summary":null,"start":23206918,"end":23207369,"strand":1,"description":"ribosomal protein L23a pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:35997]"}, {"versioned_ensembl_gene_id":"ENSG00000250714.3","gene_symbol":"AC100861.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23225233,"end":23230915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253930.1","gene_symbol":"TNFRSF10A-AS1","gene_name":"TNFRSF10A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53164]","synonyms":"RP11-1149O23.2","biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23189279,"end":23190675,"strand":1,"description":"TNFRSF10A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:53164]"}, {"versioned_ensembl_gene_id":"ENSG00000246582.2","gene_symbol":"AC100861.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":23224471,"end":23230926,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228575.9","gene_symbol":"MDC1","gene_name":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]","synonyms":"KIAA0170,Em:AB023051.5,NFBD1","biotype":"protein_coding","ncbi_id":"9656","summary":"The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci. [provided by RefSeq, Jul 2008]","start":30744466,"end":30762547,"strand":-1,"description":"mediator of DNA damage checkpoint 1 [Source:HGNC Symbol;Acc:HGNC:21163]"}, {"versioned_ensembl_gene_id":"ENSG00000084774.13","gene_symbol":"CAD","gene_name":"carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [Source:HGNC Symbol;Acc:HGNC:1424]","synonyms":"GATD4","biotype":"protein_coding","ncbi_id":"790","summary":"The de novo synthesis of pyrimidine nucleotides is required for mammalian cells to proliferate. This gene encodes a trifunctional protein which is associated with the enzymatic activities of the first 3 enzymes in the 6-step pathway of pyrimidine biosynthesis: carbamoylphosphate synthetase (CPS II), aspartate transcarbamoylase, and dihydroorotase. This protein is regulated by the mitogen-activated protein kinase (MAPK) cascade, which indicates a direct link between activation of the MAPK cascade and de novo biosynthesis of pyrimidine nucleotides. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]","start":27217390,"end":27243943,"strand":1,"description":"carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [Source:HGNC Symbol;Acc:HGNC:1424]"}, {"versioned_ensembl_gene_id":"ENSG00000175197.11","gene_symbol":"DDIT3","gene_name":"DNA damage inducible transcript 3 [Source:HGNC Symbol;Acc:HGNC:2726]","synonyms":"GADD153,CHOP10,CHOP","biotype":"protein_coding","ncbi_id":"1649","summary":"This gene encodes a member of the CCAAT/enhancer-binding protein (C/EBP) family of transcription factors. The protein functions as a dominant-negative inhibitor by forming heterodimers with other C/EBP members, such as C/EBP and LAP (liver activator protein), and preventing their DNA binding activity. The protein is implicated in adipogenesis and erythropoiesis, is activated by endoplasmic reticulum stress, and promotes apoptosis. Fusion of this gene and FUS on chromosome 16 or EWSR1 on chromosome 22 induced by translocation generates chimeric proteins in myxoid liposarcomas or Ewing sarcoma. Multiple alternatively spliced transcript variants encoding two isoforms with different length have been identified. [provided by RefSeq, Aug 2010]","start":57516588,"end":57520517,"strand":-1,"description":"DNA damage inducible transcript 3 [Source:HGNC Symbol;Acc:HGNC:2726]"}, {"versioned_ensembl_gene_id":"ENSG00000242058.2","gene_symbol":"RPS4XP19","gene_name":"ribosomal protein S4X pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36872]","synonyms":"RPS4P19","biotype":"processed_pseudogene","ncbi_id":"645573","summary":null,"start":9020029,"end":9020764,"strand":1,"description":"ribosomal protein S4X pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:36872]"}, {"versioned_ensembl_gene_id":"ENSG00000104689.9","gene_symbol":"TNFRSF10A","gene_name":"TNF receptor superfamily member 10a [Source:HGNC Symbol;Acc:HGNC:11904]","synonyms":"TRAILR-1,DR4,CD261,Apo2","biotype":"protein_coding","ncbi_id":"8797","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008]","start":23190452,"end":23225126,"strand":-1,"description":"TNF receptor superfamily member 10a [Source:HGNC Symbol;Acc:HGNC:11904]"}, {"versioned_ensembl_gene_id":"ENSG00000169789.10","gene_symbol":"PRY","gene_name":"PTPN13-like, Y-linked [Source:HGNC Symbol;Acc:HGNC:14024]","synonyms":"PTPN13LY,PRY1","biotype":"protein_coding","ncbi_id":"9081","summary":"This gene is located in the nonrecombining portion of the Y chromosome, and expressed specifically in testis. It encodes a protein which has a low degree of similarity to protein tyrosine phosphatase, non-receptor type 13. Two nearly identical copies of this gene exist within a palindromic region. This record represents the more telomeric copy. [provided by RefSeq, Jul 2008]","start":22490397,"end":22514637,"strand":1,"description":"PTPN13-like, Y-linked [Source:HGNC Symbol;Acc:HGNC:14024]"}, {"versioned_ensembl_gene_id":"ENSG00000139116.18","gene_symbol":"KIF21A","gene_name":"kinesin family member 21A [Source:HGNC Symbol;Acc:HGNC:19349]","synonyms":"FLJ20052,FEOM1","biotype":"protein_coding","ncbi_id":"55605","summary":"This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]","start":39293228,"end":39443390,"strand":-1,"description":"kinesin family member 21A [Source:HGNC Symbol;Acc:HGNC:19349]"}, {"versioned_ensembl_gene_id":"ENSG00000005448.16","gene_symbol":"WDR54","gene_name":"WD repeat domain 54 [Source:HGNC Symbol;Acc:HGNC:25770]","synonyms":"FLJ12953","biotype":"protein_coding","ncbi_id":"84058","summary":null,"start":74421678,"end":74425755,"strand":1,"description":"WD repeat domain 54 [Source:HGNC Symbol;Acc:HGNC:25770]"}, {"versioned_ensembl_gene_id":"ENSG00000266261.1","gene_symbol":"AC005324.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15651590,"end":15654489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181029.8","gene_symbol":"TRAPPC5","gene_name":"trafficking protein particle complex 5 [Source:HGNC Symbol;Acc:HGNC:23067]","synonyms":"TRS31,MGC52424","biotype":"protein_coding","ncbi_id":"126003","summary":null,"start":7680843,"end":7687703,"strand":1,"description":"trafficking protein particle complex 5 [Source:HGNC Symbol;Acc:HGNC:23067]"}, {"versioned_ensembl_gene_id":"ENSG00000221926.11","gene_symbol":"TRIM16","gene_name":"tripartite motif containing 16 [Source:HGNC Symbol;Acc:HGNC:17241]","synonyms":"EBBP","biotype":"protein_coding","ncbi_id":"10626","summary":"The protein encoded by this gene is a tripartite motif (TRIM) family member that contains two B box domains and a coiled-coiled region that are characteristic of the B box zinc finger protein family. While it lacks a RING domain found in other TRIM proteins, the encoded protein can homodimerize or heterodimerize with other TRIM proteins and has E3 ubiquitin ligase activity. This gene is also a tumor suppressor and is involved in secretory autophagy. [provided by RefSeq, Jan 2017]","start":15627960,"end":15684311,"strand":-1,"description":"tripartite motif containing 16 [Source:HGNC Symbol;Acc:HGNC:17241]"}, {"versioned_ensembl_gene_id":"ENSG00000249077.1","gene_symbol":"AL158068.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2324467,"end":2325082,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159733.13","gene_symbol":"ZFYVE28","gene_name":"zinc finger FYVE-type containing 28 [Source:HGNC Symbol;Acc:HGNC:29334]","synonyms":"KIAA1643","biotype":"protein_coding","ncbi_id":"57732","summary":null,"start":2269582,"end":2418663,"strand":-1,"description":"zinc finger FYVE-type containing 28 [Source:HGNC Symbol;Acc:HGNC:29334]"}, {"versioned_ensembl_gene_id":"ENSG00000279202.1","gene_symbol":"AC130448.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":24098239,"end":24099971,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251600.6","gene_symbol":"AC139713.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":143559457,"end":144188367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259018.1","gene_symbol":"AL049829.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23356406,"end":23357003,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100842.12","gene_symbol":"EFS","gene_name":"embryonal Fyn-associated substrate [Source:HGNC Symbol;Acc:HGNC:16898]","synonyms":"EFS2,EFS1,CASS3,SIN,HEFS","biotype":"protein_coding","ncbi_id":"10278","summary":"The protein encoded by this gene is a member of the CAS (CRK-associated substrate) family of adaptor proteins which typically serve as scaffolds for the assembly of larger signaling complexes. These complexes form at the cell surface where integrin binding leads to the subsequent phosphorylation of a CAS protein. Additional binding of SRC family kinases leads to CAS hyperphosphorylation and the creation of binding sites for CRK and other proteins that cause actin cytoskeleton reorganization. This gene plays a role in integrin-mediated cell attachment, spreading, and migration and also plays a role in both normal and malignant cellular transformation. This broadly expressed gene has been shown to play a role in neurite outgrowth and its expression in the thymus and lymphocytes is important for T cell maturation and the development of immunological self-tolerance. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2020]","start":23356402,"end":23365752,"strand":-1,"description":"embryonal Fyn-associated substrate [Source:HGNC Symbol;Acc:HGNC:16898]"}, {"versioned_ensembl_gene_id":"ENSG00000073734.8","gene_symbol":"ABCB11","gene_name":"ATP binding cassette subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:42]","synonyms":"ABC16,SPGP,PGY4,PFIC2,PFIC-2,BSEP","biotype":"protein_coding","ncbi_id":"8647","summary":"The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008]","start":168922938,"end":169031322,"strand":-1,"description":"ATP binding cassette subfamily B member 11 [Source:HGNC Symbol;Acc:HGNC:42]"}, {"versioned_ensembl_gene_id":"ENSG00000274675.4","gene_symbol":"GTF2H2C_2","gene_name":"GTF2H2 family member C, copy 2 [Source:HGNC Symbol;Acc:HGNC:35418]","synonyms":"LOC730394,GTF2H2D","biotype":"protein_coding","ncbi_id":"730394","summary":null,"start":70182128,"end":70214752,"strand":-1,"description":"GTF2H2 family member C, copy 2 [Source:HGNC Symbol;Acc:HGNC:35418]"}, {"versioned_ensembl_gene_id":"ENSG00000124215.16","gene_symbol":"CDH26","gene_name":"cadherin 26 [Source:HGNC Symbol;Acc:HGNC:15902]","synonyms":"VR20","biotype":"protein_coding","ncbi_id":"60437","summary":"This gene encodes a member of the cadherin protein family. Cadherins are a family of calcium-dependent adhesion molecules that mediate cell-cell adhesion in all solid tissues and modulate a wide variety of processes, including cell polarization, migration and differentiation. Cadherin domains occur as repeats in the extracellular region and are thought to contribute to the sorting of heterogeneous cell types and the maintenance of orderly structures such as epithelium. This protein is expressed in gastrointestinal epithelial cells and may be upregulated during allergic inflammation. This protein interacts with alpha integrins and may also be involved in leukocyte migration and adhesion. [provided by RefSeq, Jan 2017]","start":59958427,"end":60034011,"strand":1,"description":"cadherin 26 [Source:HGNC Symbol;Acc:HGNC:15902]"}, {"versioned_ensembl_gene_id":"ENSG00000224790.2","gene_symbol":"AP000704.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36966492,"end":36975164,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270652.1","gene_symbol":"DPRXP5","gene_name":"divergent-paired related homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32171]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503646","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DPRX homeobox gene family. [provided by RefSeq, Jul 2008]","start":36943267,"end":36944125,"strand":1,"description":"divergent-paired related homeobox pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:32171]"}, {"versioned_ensembl_gene_id":"ENSG00000237646.1","gene_symbol":"HLCS-IT1","gene_name":"HLCS intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41343]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874294","summary":null,"start":36803984,"end":36806284,"strand":-1,"description":"HLCS intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41343]"}, {"versioned_ensembl_gene_id":"ENSG00000236512.1","gene_symbol":"AL390026.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7620422,"end":7620878,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267077.1","gene_symbol":"AC020663.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":4795265,"end":4796532,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271414.1","gene_symbol":"AC093107.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135650972,"end":135651416,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000159267.14","gene_symbol":"HLCS","gene_name":"holocarboxylase synthetase [Source:HGNC Symbol;Acc:HGNC:4976]","synonyms":"HCS","biotype":"protein_coding","ncbi_id":"3141","summary":"This gene encodes an enzyme that catalyzes the binding of biotin to carboxylases and histones. The protein plays an important role in gluconeogenesis, fatty acid synthesis and branched chain amino acid catabolism. Defects in this gene are the cause of holocarboxylase synthetase deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jun 2011]","start":36750888,"end":36990236,"strand":-1,"description":"holocarboxylase synthetase [Source:HGNC Symbol;Acc:HGNC:4976]"}, {"versioned_ensembl_gene_id":"ENSG00000223718.3","gene_symbol":"AC093107.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":135660039,"end":135660647,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250406.1","gene_symbol":"AC109811.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144851572,"end":144874787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249193.1","gene_symbol":"HSPD1P5","gene_name":"heat shock protein family D (Hsp60) member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5266]","synonyms":"HSPD1-8P,HSPDP5","biotype":"processed_pseudogene","ncbi_id":"345041","summary":null,"start":144845625,"end":144847344,"strand":1,"description":"heat shock protein family D (Hsp60) member 1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:5266]"}, {"versioned_ensembl_gene_id":"ENSG00000080345.17","gene_symbol":"RIF1","gene_name":"replication timing regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:23207]","synonyms":"FLJ12870,FLJ10599","biotype":"protein_coding","ncbi_id":"55183","summary":"This gene encodes a protein that shares homology with the yeast teleomere binding protein, Rap1 interacting factor 1. This protein localizes to aberrant telomeres may be involved in DNA repair. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]","start":151409883,"end":151508013,"strand":1,"description":"replication timing regulatory factor 1 [Source:HGNC Symbol;Acc:HGNC:23207]"}, {"versioned_ensembl_gene_id":"ENSG00000238072.1","gene_symbol":"AC009244.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129410113,"end":129410370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248890.1","gene_symbol":"HHIP-AS1","gene_name":"HHIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44182]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"646576","summary":null,"start":144642922,"end":144661357,"strand":-1,"description":"HHIP antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44182]"}, {"versioned_ensembl_gene_id":"ENSG00000158467.16","gene_symbol":"AHCYL2","gene_name":"adenosylhomocysteinase like 2 [Source:HGNC Symbol;Acc:HGNC:22204]","synonyms":"KIAA0828","biotype":"protein_coding","ncbi_id":"23382","summary":"The protein encoded by this gene acts as a homotetramer and may be involved in the conversion of S-adenosyl-L-homocysteine to L-homocysteine and adenosine. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]","start":129225023,"end":129430211,"strand":1,"description":"adenosylhomocysteinase like 2 [Source:HGNC Symbol;Acc:HGNC:22204]"}, {"versioned_ensembl_gene_id":"ENSG00000178026.12","gene_symbol":"LRRC75B","gene_name":"leucine rich repeat containing 75B [Source:HGNC Symbol;Acc:HGNC:33155]","synonyms":"C22orf36,MGC131773,FAM211B","biotype":"protein_coding","ncbi_id":"388886","summary":null,"start":24585620,"end":24593208,"strand":-1,"description":"leucine rich repeat containing 75B [Source:HGNC Symbol;Acc:HGNC:33155]"}, {"versioned_ensembl_gene_id":"ENSG00000183090.5","gene_symbol":"FREM3","gene_name":"FRAS1 related extracellular matrix 3 [Source:HGNC Symbol;Acc:HGNC:25172]","synonyms":null,"biotype":"protein_coding","ncbi_id":"166752","summary":"This gene encodes an integral membrane protein containing numerous CSPG (chondroitin sulfate proteoglycan element) repeats and Calx-beta domains. The protein belongs to the family of FRAS1/FREM extracellular matrix proteins and may play a role cell adhesion. [provided by RefSeq, Feb 2017]","start":143577302,"end":143700675,"strand":-1,"description":"FRAS1 related extracellular matrix 3 [Source:HGNC Symbol;Acc:HGNC:25172]"}, {"versioned_ensembl_gene_id":"ENSG00000184344.3","gene_symbol":"GDF3","gene_name":"growth differentiation factor 3 [Source:HGNC Symbol;Acc:HGNC:4218]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9573","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein plays a role ocular and skeletal development. Mutations in this gene are associated with microphthalmia, coloboma, and skeletal abnormalities in human patients. [provided by RefSeq, Aug 2016]","start":7689782,"end":7695776,"strand":-1,"description":"growth differentiation factor 3 [Source:HGNC Symbol;Acc:HGNC:4218]"}, {"versioned_ensembl_gene_id":"ENSG00000273226.1","gene_symbol":"AL391834.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19375451,"end":19375996,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137154.12","gene_symbol":"RPS6","gene_name":"ribosomal protein S6 [Source:HGNC Symbol;Acc:HGNC:10429]","synonyms":"S6","biotype":"protein_coding","ncbi_id":"6194","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a cytoplasmic ribosomal protein that is a component of the 40S subunit. The protein belongs to the S6E family of ribosomal proteins. It is the major substrate of protein kinases in the ribosome, with subsets of five C-terminal serine residues phosphorylated by different protein kinases. Phosphorylation is induced by a wide range of stimuli, including growth factors, tumor-promoting agents, and mitogens. Dephosphorylation occurs at growth arrest. The protein may contribute to the control of cell growth and proliferation through the selective translation of particular classes of mRNA. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":19375715,"end":19380254,"strand":-1,"description":"ribosomal protein S6 [Source:HGNC Symbol;Acc:HGNC:10429]"}, {"versioned_ensembl_gene_id":"ENSG00000282052.1","gene_symbol":"RPS7P11","gene_name":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644315","summary":null,"start":46550508,"end":46551093,"strand":-1,"description":"ribosomal protein S7 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:35841]"}, {"versioned_ensembl_gene_id":"ENSG00000133740.10","gene_symbol":"E2F5","gene_name":"E2F transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:3119]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1875","summary":"The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionarily conserved domains that are present in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein is differentially phosphorylated and is expressed in a wide variety of human tissues. It has higher identity to E2F4 than to other family members. Both this protein and E2F4 interact with tumor suppressor proteins p130 and p107, but not with pRB. Alternative splicing results in multiple variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":85177225,"end":85217158,"strand":1,"description":"E2F transcription factor 5 [Source:HGNC Symbol;Acc:HGNC:3119]"}, {"versioned_ensembl_gene_id":"ENSG00000261129.1","gene_symbol":"AC106871.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":144505900,"end":144509001,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000149651.3","gene_symbol":"SPINT4","gene_name":"serine peptidase inhibitor, Kunitz type 4 [Source:HGNC Symbol;Acc:HGNC:16130]","synonyms":"dJ601O1.1,C20orf137","biotype":"protein_coding","ncbi_id":"391253","summary":null,"start":45722351,"end":45725830,"strand":1,"description":"serine peptidase inhibitor, Kunitz type 4 [Source:HGNC Symbol;Acc:HGNC:16130]"}, {"versioned_ensembl_gene_id":"ENSG00000224508.1","gene_symbol":"MDC1-AS1","gene_name":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]","synonyms":"MDC1-AS","biotype":"processed_transcript","ncbi_id":"106478956","summary":null,"start":30747726,"end":30757842,"strand":1,"description":"MDC1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39764]"}, {"versioned_ensembl_gene_id":"ENSG00000164163.10","gene_symbol":"ABCE1","gene_name":"ATP binding cassette subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:69]","synonyms":"RLI,OABP,RNS4I,RNASELI,RNASEL1,RLI1","biotype":"protein_coding","ncbi_id":"6059","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the OABP subfamily. Alternatively referred to as the RNase L inhibitor, this protein functions to block the activity of ribonuclease L. Activation of ribonuclease L leads to inhibition of protein synthesis in the 2-5A/RNase L system, the central pathway for viral interferon action. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":145097932,"end":145129179,"strand":1,"description":"ATP binding cassette subfamily E member 1 [Source:HGNC Symbol;Acc:HGNC:69]"}, {"versioned_ensembl_gene_id":"ENSG00000100219.16","gene_symbol":"XBP1","gene_name":"X-box binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12801]","synonyms":"XBP2","biotype":"protein_coding","ncbi_id":"7494","summary":"This gene encodes a transcription factor that regulates MHC class II genes by binding to a promoter element referred to as an X box. This gene product is a bZIP protein, which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter. It may increase expression of viral proteins by acting as the DNA binding partner of a viral transactivator. It has been found that upon accumulation of unfolded proteins in the endoplasmic reticulum (ER), the mRNA of this gene is processed to an active form by an unconventional splicing mechanism that is mediated by the endonuclease inositol-requiring enzyme 1 (IRE1). The resulting loss of 26 nt from the spliced mRNA causes a frame-shift and an isoform XBP1(S), which is the functionally active transcription factor. The isoform encoded by the unspliced mRNA, XBP1(U), is constitutively expressed, and thought to function as a negative feedback regulator of XBP1(S), which shuts off transcription of target genes during the recovery phase of ER stress. A pseudogene of XBP1 has been identified and localized to chromosome 5. [provided by RefSeq, Jul 2008]","start":28794555,"end":28800597,"strand":-1,"description":"X-box binding protein 1 [Source:HGNC Symbol;Acc:HGNC:12801]"}, {"versioned_ensembl_gene_id":"ENSG00000232956.8","gene_symbol":"SNHG15","gene_name":"small nucleolar RNA host gene 15 [Source:HGNC Symbol;Acc:HGNC:27797]","synonyms":"MYO1GUT,Linc-Myo1g,FLJ38860,C7orf40","biotype":"lincRNA","ncbi_id":"285958","summary":"This gene represents a snoRNA host gene that produces a short-lived long non-coding RNA. This non-coding RNA is upregulated in tumor cells and may contribute to cell proliferation by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017]","start":44983023,"end":44986961,"strand":-1,"description":"small nucleolar RNA host gene 15 [Source:HGNC Symbol;Acc:HGNC:27797]"}, {"versioned_ensembl_gene_id":"ENSG00000236555.1","gene_symbol":"AC115115.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112346011,"end":112346258,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174640.12","gene_symbol":"SLCO2A1","gene_name":"solute carrier organic anion transporter family member 2A1 [Source:HGNC Symbol;Acc:HGNC:10955]","synonyms":"SLC21A2,PGT,OATP2A1,MATR1","biotype":"protein_coding","ncbi_id":"6578","summary":"This gene encodes a prostaglandin transporter that is a member of the 12-membrane-spanning superfamily of transporters. The encoded protein may be involved in mediating the uptake and clearance of prostaglandins in numerous tissues. [provided by RefSeq, Dec 2011]","start":133932696,"end":134052184,"strand":-1,"description":"solute carrier organic anion transporter family member 2A1 [Source:HGNC Symbol;Acc:HGNC:10955]"}, {"versioned_ensembl_gene_id":"ENSG00000173137.11","gene_symbol":"ADCK5","gene_name":"aarF domain containing kinase 5 [Source:HGNC Symbol;Acc:HGNC:21738]","synonyms":"FLJ35454","biotype":"protein_coding","ncbi_id":"203054","summary":null,"start":144373101,"end":144393242,"strand":1,"description":"aarF domain containing kinase 5 [Source:HGNC Symbol;Acc:HGNC:21738]"}, {"versioned_ensembl_gene_id":"ENSG00000226188.2","gene_symbol":"HNRNPA1P3","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16567]","synonyms":"HNRPA1P3,dJ447F3.1","biotype":"processed_pseudogene","ncbi_id":"170524","summary":null,"start":45745737,"end":45746287,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16567]"}, {"versioned_ensembl_gene_id":"ENSG00000280018.3","gene_symbol":"CU634019.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6986450,"end":6997765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279313.1","gene_symbol":"CU634019.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6994374,"end":6997737,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100028.11","gene_symbol":"SNRPD3","gene_name":"small nuclear ribonucleoprotein D3 polypeptide [Source:HGNC Symbol;Acc:HGNC:11160]","synonyms":"SMD3,Sm-D3","biotype":"protein_coding","ncbi_id":"6634","summary":"This gene encodes a core component of the spliceosome, which is a nuclear ribonucleoprotein complex that functions in pre-mRNA splicing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":24555503,"end":24609980,"strand":1,"description":"small nuclear ribonucleoprotein D3 polypeptide [Source:HGNC Symbol;Acc:HGNC:11160]"}, {"versioned_ensembl_gene_id":"ENSG00000279477.1","gene_symbol":"CU634019.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7003248,"end":7007022,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231580.1","gene_symbol":"CR759904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33118526,"end":33118935,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257219.5","gene_symbol":"LINC02407","gene_name":"long intergenic non-protein coding RNA 2407 [Source:HGNC Symbol;Acc:HGNC:53336]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369848","summary":null,"start":76259839,"end":76305131,"strand":1,"description":"long intergenic non-protein coding RNA 2407 [Source:HGNC Symbol;Acc:HGNC:53336]"}, {"versioned_ensembl_gene_id":"ENSG00000275498.5","gene_symbol":"PDXDC1","gene_name":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]","synonyms":"KIAA0251,KIAA0251","biotype":"protein_coding","ncbi_id":"23042","summary":null,"start":15058498,"end":15122225,"strand":-1,"description":"pyridoxal dependent decarboxylase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28995]"}, {"versioned_ensembl_gene_id":"ENSG00000235844.8","gene_symbol":"HLA-DPA1","gene_name":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]","synonyms":"HLA-DP1A","biotype":"protein_coding","ncbi_id":"3113","summary":"HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33103656,"end":33119850,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 1 [Source:HGNC Symbol;Acc:HGNC:4938]"}, {"versioned_ensembl_gene_id":"ENSG00000278884.1","gene_symbol":"CU634019.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7020599,"end":7025166,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244480.1","gene_symbol":"AC005154.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":30523143,"end":30524535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280501.2","gene_symbol":"CEACAM7","gene_name":"carcinoembryonic antigen related cell adhesion molecule 7 [Source:HGNC Symbol;Acc:HGNC:1819]","synonyms":"CGM2,CEA","biotype":"protein_coding","ncbi_id":"1087","summary":"This gene encodes a cell surface glycoprotein and member of the carcinoembryonic antigen (CEA) family of proteins. Expression of this gene may be downregulated in colon and rectal cancer. Additionally, lower expression levels of this gene may be predictive of rectal cancer recurrence. This gene is present in a CEA family gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]","start":41681649,"end":41685845,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 7 [Source:HGNC Symbol;Acc:HGNC:1819]"}, {"versioned_ensembl_gene_id":"ENSG00000281039.1","gene_symbol":"AC005154.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30497077,"end":30550761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263683.1","gene_symbol":"AC005154.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30550217,"end":30551569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179941.6","gene_symbol":"BBS10","gene_name":"Bardet-Biedl syndrome 10 [Source:HGNC Symbol;Acc:HGNC:26291]","synonyms":"FLJ23560,C12orf58","biotype":"protein_coding","ncbi_id":"79738","summary":"This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10. [provided by RefSeq, Jan 2010]","start":76344474,"end":76348442,"strand":-1,"description":"Bardet-Biedl syndrome 10 [Source:HGNC Symbol;Acc:HGNC:26291]"}, {"versioned_ensembl_gene_id":"ENSG00000006625.17","gene_symbol":"GGCT","gene_name":"gamma-glutamylcyclotransferase [Source:HGNC Symbol;Acc:HGNC:21705]","synonyms":"MGC3077,Ggc,GCTG,CRF21,C7orf24","biotype":"protein_coding","ncbi_id":"79017","summary":"The protein encoded by this gene catalyzes the formation of 5-oxoproline from gamma-glutamyl dipeptides, the penultimate step in glutathione catabolism, and may play a critical role in glutathione homeostasis. The encoded protein may also play a role in cell proliferation, and the expression of this gene is a potential marker for cancer. Pseudogenes of this gene are located on the long arm of chromosome 5 and the short arm of chromosomes 2 and 20. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":30496621,"end":30504844,"strand":-1,"description":"gamma-glutamylcyclotransferase [Source:HGNC Symbol;Acc:HGNC:21705]"}, {"versioned_ensembl_gene_id":"ENSG00000223810.2","gene_symbol":"KRT8P28","gene_name":"keratin 8 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:33380]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391099","summary":null,"start":151949523,"end":151950912,"strand":-1,"description":"keratin 8 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:33380]"}, {"versioned_ensembl_gene_id":"ENSG00000229728.1","gene_symbol":"AL136531.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1361622,"end":1362585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231345.3","gene_symbol":"BEND3P1","gene_name":"BEN domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45014]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"644459","summary":null,"start":50655967,"end":50660472,"strand":1,"description":"BEN domain containing 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45014]"}, {"versioned_ensembl_gene_id":"ENSG00000125775.14","gene_symbol":"SDCBP2","gene_name":"syndecan binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15756]","synonyms":"ST-2,SITAC18","biotype":"protein_coding","ncbi_id":"27111","summary":"The protein encoded by this gene contains two class II PDZ domains. PDZ domains facilitate protein-protein interactions by binding to the cytoplasmic C-terminus of transmembrane proteins, and PDZ-containing proteins mediate cell signaling and the organization of protein complexes. The encoded protein binds to phosphatidylinositol 4, 5-bisphosphate (PIP2) and plays a role in nuclear PIP2 organization and cell division. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Read-through transcription also exists between this gene and the upstream FKBP1A (FK506 binding protein 1A, 12kDa) gene, as represented in GeneID:100528031. [provided by RefSeq, Sep 2011]","start":1309909,"end":1329239,"strand":-1,"description":"syndecan binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15756]"}, {"versioned_ensembl_gene_id":"ENSG00000236296.8","gene_symbol":"GUSBP5","gene_name":"glucuronidase, beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42319]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"441046","summary":null,"start":143559472,"end":143561460,"strand":1,"description":"glucuronidase, beta pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42319]"}, {"versioned_ensembl_gene_id":"ENSG00000197747.8","gene_symbol":"S100A10","gene_name":"S100 calcium binding protein A10 [Source:HGNC Symbol;Acc:HGNC:10487]","synonyms":"P11,CLP11,CAL1L,ANX2LG,42C","biotype":"protein_coding","ncbi_id":"6281","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in exocytosis and endocytosis. [provided by RefSeq, Jul 2008]","start":151982915,"end":151994390,"strand":-1,"description":"S100 calcium binding protein A10 [Source:HGNC Symbol;Acc:HGNC:10487]"}, {"versioned_ensembl_gene_id":"ENSG00000241456.1","gene_symbol":"AC005996.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151427683,"end":151439124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127377.8","gene_symbol":"CRYGN","gene_name":"crystallin gamma N [Source:HGNC Symbol;Acc:HGNC:20458]","synonyms":null,"biotype":"protein_coding","ncbi_id":"155051","summary":"This gene encodes a member of the crystallin family of proteins that are localized to the refractive structure of vertebrate eye lenses. The protein encoded by this gene is unique in that it has both beta and gamma crystallin protein motifs. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":151428835,"end":151440813,"strand":-1,"description":"crystallin gamma N [Source:HGNC Symbol;Acc:HGNC:20458]"}, {"versioned_ensembl_gene_id":"ENSG00000138867.16","gene_symbol":"GUCD1","gene_name":"guanylyl cyclase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14237]","synonyms":"MGC1842,LLN4,C22orf13","biotype":"protein_coding","ncbi_id":"83606","summary":null,"start":24540423,"end":24555935,"strand":-1,"description":"guanylyl cyclase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14237]"}, {"versioned_ensembl_gene_id":"ENSG00000271236.1","gene_symbol":"SUMO2P15","gene_name":"SUMO2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49353]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480417","summary":null,"start":40760597,"end":40760874,"strand":1,"description":"SUMO2 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:49353]"}, {"versioned_ensembl_gene_id":"ENSG00000251136.8","gene_symbol":"AF117829.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":89609409,"end":89757727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109911.18","gene_symbol":"ELP4","gene_name":"elongator acetyltransferase complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:1171]","synonyms":"PAXNEB,C11orf19","biotype":"protein_coding","ncbi_id":"26610","summary":"This gene encodes a component of the six subunit elongator complex, a histone acetyltransferase complex that associates directly with RNA polymerase II during transcriptional elongation. The human gene can partially complement sensitivity phenotypes of yeast ELP4 deletion mutants. This gene has also been associated with Rolandic epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":31509700,"end":31790328,"strand":1,"description":"elongator acetyltransferase complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:1171]"}, {"versioned_ensembl_gene_id":"ENSG00000176971.3","gene_symbol":"FIBIN","gene_name":"fin bud initiation factor homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:33747]","synonyms":"MGC24932","biotype":"protein_coding","ncbi_id":"387758","summary":null,"start":26994184,"end":26996121,"strand":1,"description":"fin bud initiation factor homolog (zebrafish) [Source:HGNC Symbol;Acc:HGNC:33747]"}, {"versioned_ensembl_gene_id":"ENSG00000232706.3","gene_symbol":"NUTM2HP","gene_name":"NUT family member 2H, pseudogene [Source:HGNC Symbol;Acc:HGNC:45017]","synonyms":"FAM22HP","biotype":"unprocessed_pseudogene","ncbi_id":"729023","summary":null,"start":50676743,"end":50686326,"strand":1,"description":"NUT family member 2H, pseudogene [Source:HGNC Symbol;Acc:HGNC:45017]"}, {"versioned_ensembl_gene_id":"ENSG00000236693.11","gene_symbol":"HLA-DPB1","gene_name":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]","synonyms":"HLA-DP1B","biotype":"protein_coding","ncbi_id":"3115","summary":"HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]","start":33114995,"end":33126260,"strand":1,"description":"major histocompatibility complex, class II, DP beta 1 [Source:HGNC Symbol;Acc:HGNC:4940]"}, {"versioned_ensembl_gene_id":"ENSG00000008869.11","gene_symbol":"HEATR5B","gene_name":"HEAT repeat containing 5B [Source:HGNC Symbol;Acc:HGNC:29273]","synonyms":"DKFZp686P15184,KIAA1414","biotype":"protein_coding","ncbi_id":"54497","summary":null,"start":36968383,"end":37084342,"strand":-1,"description":"HEAT repeat containing 5B [Source:HGNC Symbol;Acc:HGNC:29273]"}, {"versioned_ensembl_gene_id":"ENSG00000281424.1","gene_symbol":"AC243960.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41661018,"end":41661305,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271081.1","gene_symbol":"AC009314.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30754236,"end":30754539,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104691.14","gene_symbol":"UBXN8","gene_name":"UBX domain protein 8 [Source:HGNC Symbol;Acc:HGNC:30307]","synonyms":"UBXD6,REP8,D8S2298E","biotype":"protein_coding","ncbi_id":"7993","summary":"p97 or VCP (valosin-containing protein) is a versatile ATPase complex, and many cofactors are required for the p97 functional diversity. This gene encodes one of the p97 cofactors. This cofactor is a transmembrane protein and localized in the endoplasmic reticulum (ER) membrane. It tethers p97 to the ER membrane via its UBX domain. The association of this cofactor with p97 facilitates efficient ER-associated degradation of misfolded proteins. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2013]","start":30732247,"end":30767006,"strand":1,"description":"UBX domain protein 8 [Source:HGNC Symbol;Acc:HGNC:30307]"}, {"versioned_ensembl_gene_id":"ENSG00000240667.1","gene_symbol":"AL450992.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152018662,"end":152022508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226874.1","gene_symbol":"AC005154.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30544053,"end":30544431,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229021.2","gene_symbol":"AL450992.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151994531,"end":152042774,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264520.1","gene_symbol":"AC005154.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30525731,"end":30533613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163191.5","gene_symbol":"S100A11","gene_name":"S100 calcium binding protein A11 [Source:HGNC Symbol;Acc:HGNC:10488]","synonyms":"S100C","biotype":"protein_coding","ncbi_id":"6282","summary":"The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in motility, invasion, and tubulin polymerization. Chromosomal rearrangements and altered expression of this gene have been implicated in tumor metastasis. [provided by RefSeq, Jul 2008]","start":152032506,"end":152047907,"strand":-1,"description":"S100 calcium binding protein A11 [Source:HGNC Symbol;Acc:HGNC:10488]"}, {"versioned_ensembl_gene_id":"ENSG00000196295.11","gene_symbol":"AC005154.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":30516309,"end":30594809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134490.13","gene_symbol":"TMEM241","gene_name":"transmembrane protein 241 [Source:HGNC Symbol;Acc:HGNC:31723]","synonyms":"MGC11386,FLJ44259,C18orf45","biotype":"protein_coding","ncbi_id":"85019","summary":null,"start":23197144,"end":23437961,"strand":-1,"description":"transmembrane protein 241 [Source:HGNC Symbol;Acc:HGNC:31723]"}, {"versioned_ensembl_gene_id":"ENSG00000071894.16","gene_symbol":"CPSF1","gene_name":"cleavage and polyadenylation specific factor 1 [Source:HGNC Symbol;Acc:HGNC:2324]","synonyms":"CPSF160","biotype":"protein_coding","ncbi_id":"29894","summary":"Cleavage and polyadenylation specificity factor (CPSF) is a multisubunit complex that plays a central role in 3-prime processing of pre-mRNAs. CPSF recognizes the AAUAAA signal in the pre-mRNA and interacts with other proteins to facilitate both RNA cleavage and poly(A) synthesis. CPSF1 is the largest subunit of the CPSF complex (Murthy and Manley, 1995 [PubMed 7590244]).[supplied by OMIM, Mar 2008]","start":144393229,"end":144409349,"strand":-1,"description":"cleavage and polyadenylation specific factor 1 [Source:HGNC Symbol;Acc:HGNC:2324]"}, {"versioned_ensembl_gene_id":"ENSG00000158786.4","gene_symbol":"PLA2G2F","gene_name":"phospholipase A2 group IIF [Source:HGNC Symbol;Acc:HGNC:30040]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64600","summary":null,"start":20139326,"end":20150386,"strand":1,"description":"phospholipase A2 group IIF [Source:HGNC Symbol;Acc:HGNC:30040]"}, {"versioned_ensembl_gene_id":"ENSG00000074211.13","gene_symbol":"PPP2R2C","gene_name":"protein phosphatase 2 regulatory subunit Bgamma [Source:HGNC Symbol;Acc:HGNC:9306]","synonyms":"PR55G,PR52,MGC33570,IMYPNO,B55gamma","biotype":"protein_coding","ncbi_id":"5522","summary":"The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a gamma isoform of the regulatory subunit B55 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":6320578,"end":6563600,"strand":-1,"description":"protein phosphatase 2 regulatory subunit Bgamma [Source:HGNC Symbol;Acc:HGNC:9306]"}, {"versioned_ensembl_gene_id":"ENSG00000100991.11","gene_symbol":"TRPC4AP","gene_name":"transient receptor potential cation channel subfamily C member 4 associated protein [Source:HGNC Symbol;Acc:HGNC:16181]","synonyms":"TRRP4AP,PPP1R158,DKFZP727M231,DKFZp586C1223,dJ756N5.2,C20orf188","biotype":"protein_coding","ncbi_id":"26133","summary":null,"start":35002404,"end":35092871,"strand":-1,"description":"transient receptor potential cation channel subfamily C member 4 associated protein [Source:HGNC Symbol;Acc:HGNC:16181]"}, {"versioned_ensembl_gene_id":"ENSG00000245322.6","gene_symbol":"AC097460.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99950006,"end":100195099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243433.1","gene_symbol":"AC010973.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":151028781,"end":151029754,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254208.1","gene_symbol":"AC011773.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85177522,"end":85178150,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214967.5","gene_symbol":"NPIPA7","gene_name":"nuclear pore complex interacting protein family member A7 [Source:HGNC Symbol;Acc:HGNC:41982]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101059938","summary":null,"start":16379055,"end":16393954,"strand":1,"description":"nuclear pore complex interacting protein family member A7 [Source:HGNC Symbol;Acc:HGNC:41982]"}, {"versioned_ensembl_gene_id":"ENSG00000230907.2","gene_symbol":"FKBPL","gene_name":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]","synonyms":"DIR1,WISp39,NG7","biotype":"protein_coding","ncbi_id":"63943","summary":"The protein encoded by this gene has similarity to the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The encoded protein is thought to have a potential role in the induced radioresistance. Also it appears to have some involvement in the control of the cell cycle. [provided by RefSeq, Jul 2008]","start":32077157,"end":32078741,"strand":-1,"description":"FK506 binding protein like [Source:HGNC Symbol;Acc:HGNC:13949]"}, {"versioned_ensembl_gene_id":"ENSG00000257935.2","gene_symbol":"LHX5-AS1","gene_name":"LHX5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49570]","synonyms":"locus4010","biotype":"antisense_RNA","ncbi_id":"104355219","summary":null,"start":113472003,"end":113480624,"strand":1,"description":"LHX5 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49570]"}, {"versioned_ensembl_gene_id":"ENSG00000145358.6","gene_symbol":"DDIT4L","gene_name":"DNA damage inducible transcript 4 like [Source:HGNC Symbol;Acc:HGNC:30555]","synonyms":"Rtp801L,REDD2","biotype":"protein_coding","ncbi_id":"115265","summary":null,"start":100185870,"end":100190782,"strand":-1,"description":"DNA damage inducible transcript 4 like [Source:HGNC Symbol;Acc:HGNC:30555]"}, {"versioned_ensembl_gene_id":"ENSG00000089116.3","gene_symbol":"LHX5","gene_name":"LIM homeobox 5 [Source:HGNC Symbol;Acc:HGNC:14216]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64211","summary":"This gene encodes a protein belonging to a large protein family, members of which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in the control of differentiation and development of the forebrain. In mice, this protein is essential for the regulation of precursor cell proliferation and the control of neuronal differentiation and migration during hippocampal development. This protein is involved in learning and motor functions in adult mice. [provided by RefSeq, Jul 2008]","start":113462034,"end":113472280,"strand":-1,"description":"LIM homeobox 5 [Source:HGNC Symbol;Acc:HGNC:14216]"}, {"versioned_ensembl_gene_id":"ENSG00000187569.2","gene_symbol":"DPPA3","gene_name":"developmental pluripotency associated 3 [Source:HGNC Symbol;Acc:HGNC:19199]","synonyms":"Stella,Pgc7","biotype":"protein_coding","ncbi_id":"359787","summary":"This gene encodes a protein that in mice may function as a maternal factor during the preimplantation stage of development. In mice, this gene may play a role in transcriptional repression, cell division, and maintenance of cell pluripotentiality. In humans, related intronless loci are located on chromosomes 14 and X. [provided by RefSeq, Jul 2008]","start":7711454,"end":7717559,"strand":1,"description":"developmental pluripotency associated 3 [Source:HGNC Symbol;Acc:HGNC:19199]"}, {"versioned_ensembl_gene_id":"ENSG00000271464.1","gene_symbol":"AL031176.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112319952,"end":112320417,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271400.1","gene_symbol":"AL392112.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":112381392,"end":112382220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187823.3","gene_symbol":"RTL4","gene_name":"retrotransposon Gag like 4 [Source:HGNC Symbol;Acc:HGNC:25214]","synonyms":"SIRH11,Mart4,Mar4,FLJ46608,ZCCHC16","biotype":"protein_coding","ncbi_id":"340595","summary":null,"start":112454500,"end":112457112,"strand":1,"description":"retrotransposon Gag like 4 [Source:HGNC Symbol;Acc:HGNC:25214]"}, {"versioned_ensembl_gene_id":"ENSG00000035115.21","gene_symbol":"SH3YL1","gene_name":"SH3 and SYLF domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29546]","synonyms":"Ray,DKFZP586F1318","biotype":"protein_coding","ncbi_id":"26751","summary":null,"start":217730,"end":266398,"strand":-1,"description":"SH3 and SYLF domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29546]"}, {"versioned_ensembl_gene_id":"ENSG00000130475.14","gene_symbol":"FCHO1","gene_name":"FCH domain only 1 [Source:HGNC Symbol;Acc:HGNC:29002]","synonyms":"KIAA0290","biotype":"protein_coding","ncbi_id":"23149","summary":null,"start":17747718,"end":17788568,"strand":1,"description":"FCH domain only 1 [Source:HGNC Symbol;Acc:HGNC:29002]"}, {"versioned_ensembl_gene_id":"ENSG00000249710.1","gene_symbol":"AP001961.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":100190033,"end":100215505,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164032.11","gene_symbol":"H2AFZ","gene_name":"H2A histone family member Z [Source:HGNC Symbol;Acc:HGNC:4741]","synonyms":"H2AZ,H2A.Z","biotype":"protein_coding","ncbi_id":"3015","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent member of the histone H2A family that is distinct from other members of the family. Studies in mice have shown that this particular histone is required for embryonic development and indicate that lack of functional histone H2A leads to embryonic lethality. [provided by RefSeq, Jul 2008]","start":99948086,"end":99950388,"strand":-1,"description":"H2A histone family member Z [Source:HGNC Symbol;Acc:HGNC:4741]"}, {"versioned_ensembl_gene_id":"ENSG00000109758.8","gene_symbol":"HGFAC","gene_name":"HGF activator [Source:HGNC Symbol;Acc:HGNC:4894]","synonyms":"HGFAP,HGFA","biotype":"protein_coding","ncbi_id":"3083","summary":"This gene encodes a member of the peptidase S1 protein family. The encoded protein is first synthesized as an inactive single-chain precursor before being activated to a heterodimeric form by endoproteolytic processing. It acts as serine protease that converts hepatocyte growth factor to the active form. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":3441887,"end":3449495,"strand":1,"description":"HGF activator [Source:HGNC Symbol;Acc:HGNC:4894]"}, {"versioned_ensembl_gene_id":"ENSG00000283451.1","gene_symbol":"AC009950.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":230138601,"end":230138783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185187.12","gene_symbol":"SIGIRR","gene_name":"single Ig and TIR domain containing [Source:HGNC Symbol;Acc:HGNC:30575]","synonyms":"TIR8,IL-1R8","biotype":"protein_coding","ncbi_id":"59307","summary":null,"start":405716,"end":417455,"strand":-1,"description":"single Ig and TIR domain containing [Source:HGNC Symbol;Acc:HGNC:30575]"}, {"versioned_ensembl_gene_id":"ENSG00000149923.13","gene_symbol":"PPP4C","gene_name":"protein phosphatase 4 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9319]","synonyms":"PPX,PP4","biotype":"protein_coding","ncbi_id":"5531","summary":null,"start":30075978,"end":30085377,"strand":1,"description":"protein phosphatase 4 catalytic subunit [Source:HGNC Symbol;Acc:HGNC:9319]"}, {"versioned_ensembl_gene_id":"ENSG00000231815.1","gene_symbol":"AC007179.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59435213,"end":59442261,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271955.1","gene_symbol":"AC007100.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59218680,"end":60100200,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135899.17","gene_symbol":"SP110","gene_name":"SP110 nuclear body protein [Source:HGNC Symbol;Acc:HGNC:5401]","synonyms":"IFI75,IFI41","biotype":"protein_coding","ncbi_id":"3431","summary":"The nuclear body is a multiprotein complex that may have a role in the regulation of gene transcription. This gene is a member of the SP100/SP140 family of nuclear body proteins and encodes a leukocyte-specific nuclear body component. The protein can function as an activator of gene transcription and may serve as a nuclear hormone receptor coactivator. In addition, it has been suggested that the protein may play a role in ribosome biogenesis and in the induction of myeloid cell differentiation. Alternative splicing has been observed for this gene and three transcript variants, encoding distinct isoforms, have been identified. [provided by RefSeq, Jul 2008]","start":230167293,"end":230225729,"strand":-1,"description":"SP110 nuclear body protein [Source:HGNC Symbol;Acc:HGNC:5401]"}, {"versioned_ensembl_gene_id":"ENSG00000176659.7","gene_symbol":"C20orf197","gene_name":"chromosome 20 open reading frame 197 [Source:HGNC Symbol;Acc:HGNC:26601]","synonyms":"FLJ33860","biotype":"lincRNA","ncbi_id":"284756","summary":null,"start":60055925,"end":60072953,"strand":1,"description":"chromosome 20 open reading frame 197 [Source:HGNC Symbol;Acc:HGNC:26601]"}, {"versioned_ensembl_gene_id":"ENSG00000226168.1","gene_symbol":"AL589794.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50695592,"end":50695981,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276093.1","gene_symbol":"AL132822.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60083360,"end":60083872,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088832.16","gene_symbol":"FKBP1A","gene_name":"FK506 binding protein 1A [Source:HGNC Symbol;Acc:HGNC:3711]","synonyms":"PPIASE,PKC12,FKBP12C,FKBP12,FKBP1,FKBP-12","biotype":"protein_coding","ncbi_id":"2280","summary":"The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq, Sep 2008]","start":1368978,"end":1393172,"strand":-1,"description":"FK506 binding protein 1A [Source:HGNC Symbol;Acc:HGNC:3711]"}, {"versioned_ensembl_gene_id":"ENSG00000141646.13","gene_symbol":"SMAD4","gene_name":"SMAD family member 4 [Source:HGNC Symbol;Acc:HGNC:6770]","synonyms":"MADH4,DPC4","biotype":"protein_coding","ncbi_id":"4089","summary":"This gene encodes a member of the Smad family of signal transduction proteins. Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to transforming growth factor (TGF)-beta signaling. The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins, which then accumulate in the nucleus and regulate the transcription of target genes. This protein binds to DNA and recognizes an 8-bp palindromic sequence (GTCTAGAC) called the Smad-binding element (SBE). The protein acts as a tumor suppressor and inhibits epithelial cell proliferation. It may also have an inhibitory effect on tumors by reducing angiogenesis and increasng blood vessel hyperpermeability. The encoded protein is a crucial component of the bone morphogenetic protein signaling pathway. The Smad proteins are subject to complex regulation by post-translational modifications. Mutations or deletions in this gene have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome. [provided by RefSeq, Aug 2017]","start":51028394,"end":51085045,"strand":1,"description":"SMAD family member 4 [Source:HGNC Symbol;Acc:HGNC:6770]"}, {"versioned_ensembl_gene_id":"ENSG00000106105.13","gene_symbol":"GARS","gene_name":"glycyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:4162]","synonyms":"DSMAV,CMT2D,SMAD1,GlyRS","biotype":"protein_coding","ncbi_id":"2617","summary":"This gene encodes glycyl-tRNA synthetase, one of the aminoacyl-tRNA synthetases that charge tRNAs with their cognate amino acids. The encoded enzyme is an (alpha)2 dimer which belongs to the class II family of tRNA synthetases. It has been shown to be a target of autoantibodies in the human autoimmune diseases, polymyositis or dermatomyositis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":30594681,"end":30634033,"strand":1,"description":"glycyl-tRNA synthetase [Source:HGNC Symbol;Acc:HGNC:4162]"}, {"versioned_ensembl_gene_id":"ENSG00000248820.2","gene_symbol":"DYNLL1P6","gene_name":"dynein light chain LC8-type 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49657]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288885","summary":null,"start":100041841,"end":100042104,"strand":-1,"description":"dynein light chain LC8-type 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:49657]"}, {"versioned_ensembl_gene_id":"ENSG00000250403.1","gene_symbol":"AC097460.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":99990737,"end":99991477,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000129151.8","gene_symbol":"BBOX1","gene_name":"gamma-butyrobetaine hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:964]","synonyms":"gamma-BBH,G-BBH,BBOX,BBH","biotype":"protein_coding","ncbi_id":"8424","summary":"This gene encodes gamma butyrobetaine hydroxylase which catalyzes the formation of L-carnitine from gamma-butyrobetaine, the last step in the L-carnitine biosynthetic pathway. Carnitine is essential for the transport of activated fatty acids across the mitochondrial membrane during mitochondrial beta-oxidation. [provided by RefSeq, Jul 2008]","start":27040725,"end":27127809,"strand":1,"description":"gamma-butyrobetaine hydroxylase 1 [Source:HGNC Symbol;Acc:HGNC:964]"}, {"versioned_ensembl_gene_id":"ENSG00000206510.9","gene_symbol":"ZFP57","gene_name":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]","synonyms":"bA145L22.2,ZNF698,bA145L22,C6orf40","biotype":"protein_coding","ncbi_id":"346171","summary":"The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009]","start":29672300,"end":29681010,"strand":-1,"description":"ZFP57 zinc finger protein [Source:HGNC Symbol;Acc:HGNC:18791]"}, {"versioned_ensembl_gene_id":"ENSG00000254501.1","gene_symbol":"AP003068.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":65110714,"end":65111695,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137078.8","gene_symbol":"SIT1","gene_name":"signaling threshold regulating transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:17710]","synonyms":"SIT","biotype":"protein_coding","ncbi_id":"27240","summary":null,"start":35649295,"end":35650950,"strand":-1,"description":"signaling threshold regulating transmembrane adaptor 1 [Source:HGNC Symbol;Acc:HGNC:17710]"}, {"versioned_ensembl_gene_id":"ENSG00000003756.16","gene_symbol":"RBM5","gene_name":"RNA binding motif protein 5 [Source:HGNC Symbol;Acc:HGNC:9902]","synonyms":"LUCA15,H37","biotype":"protein_coding","ncbi_id":"10181","summary":"This gene is a candidate tumor suppressor gene which encodes a nuclear RNA binding protein that is a component of the spliceosome A complex. The encoded protein plays a role in the induction of cell cycle arrest and apoptosis through pre-mRNA splicing of multiple target genes including the tumor suppressor protein p53. This gene is located within the tumor suppressor region 3p21.3, and may play a role in the inhibition of tumor transformation and progression of several malignancies including lung cancer. [provided by RefSeq, Oct 2011]","start":50088908,"end":50119021,"strand":1,"description":"RNA binding motif protein 5 [Source:HGNC Symbol;Acc:HGNC:9902]"}, {"versioned_ensembl_gene_id":"ENSG00000185519.8","gene_symbol":"FAM131C","gene_name":"family with sequence similarity 131 member C [Source:HGNC Symbol;Acc:HGNC:26717]","synonyms":"FLJ36766,C1orf117","biotype":"protein_coding","ncbi_id":"348487","summary":null,"start":16057769,"end":16073632,"strand":-1,"description":"family with sequence similarity 131 member C [Source:HGNC Symbol;Acc:HGNC:26717]"}, {"versioned_ensembl_gene_id":"ENSG00000282295.1","gene_symbol":"PRSS3P1","gene_name":"protease, serine 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43787]","synonyms":"TRY5","biotype":"unprocessed_pseudogene","ncbi_id":"168330","summary":null,"start":142801130,"end":142804658,"strand":1,"description":"protease, serine 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43787]"}, {"versioned_ensembl_gene_id":"ENSG00000148602.5","gene_symbol":"LRIT1","gene_name":"leucine rich repeat, Ig-like and transmembrane domains 1 [Source:HGNC Symbol;Acc:HGNC:23404]","synonyms":"PAL,LRRC21,FIGLER9,DKFZP434K091","biotype":"protein_coding","ncbi_id":"26103","summary":null,"start":84231593,"end":84241461,"strand":-1,"description":"leucine rich repeat, Ig-like and transmembrane domains 1 [Source:HGNC Symbol;Acc:HGNC:23404]"}, {"versioned_ensembl_gene_id":"ENSG00000182508.13","gene_symbol":"LHFPL1","gene_name":"LHFPL tetraspan subfamily member 1 [Source:HGNC Symbol;Acc:HGNC:6587]","synonyms":null,"biotype":"protein_coding","ncbi_id":"340596","summary":"This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":112630648,"end":112680054,"strand":-1,"description":"LHFPL tetraspan subfamily member 1 [Source:HGNC Symbol;Acc:HGNC:6587]"}, {"versioned_ensembl_gene_id":"ENSG00000213652.3","gene_symbol":"HMGB3P30","gene_name":"high mobility group box 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39333]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"203510","summary":null,"start":112689915,"end":112690520,"strand":1,"description":"high mobility group box 3 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39333]"}, {"versioned_ensembl_gene_id":"ENSG00000147164.11","gene_symbol":"SNX12","gene_name":"sorting nexin 12 [Source:HGNC Symbol;Acc:HGNC:14976]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29934","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. A similar protein in mouse may be involved in regulating the neurite outgrowth. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]","start":71056332,"end":71073426,"strand":-1,"description":"sorting nexin 12 [Source:HGNC Symbol;Acc:HGNC:14976]"}, {"versioned_ensembl_gene_id":"ENSG00000223979.2","gene_symbol":"SMCR2","gene_name":"Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17914]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371564","summary":null,"start":17674026,"end":17677688,"strand":-1,"description":"Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17914]"}, {"versioned_ensembl_gene_id":"ENSG00000251148.1","gene_symbol":"AL158068.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2295584,"end":2319089,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000078814.15","gene_symbol":"MYH7B","gene_name":"myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]","synonyms":"MYH14,MHC14,KIAA1512,dJ756N5.1","biotype":"protein_coding","ncbi_id":"57644","summary":"The myosin II molecule is a multi-subunit complex consisting of two heavy chains and four light chains. This gene encodes a heavy chain of myosin II, which is a member of the motor-domain superfamily. The heavy chain includes a globular motor domain, which catalyzes ATP hydrolysis and interacts with actin, and a tail domain in which heptad repeat sequences promote dimerization by interacting to form a rod-like alpha-helical coiled coil. This heavy chain subunit is a slow-twitch myosin. Alternatively spliced transcript variants have been found, but the full-length nature of these variants is not determined. [provided by RefSeq, Mar 2010]","start":34975403,"end":35002437,"strand":1,"description":"myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]"}, {"versioned_ensembl_gene_id":"ENSG00000236251.6","gene_symbol":"HSPA1L","gene_name":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]","synonyms":"hum70t,HSP70-HOM","biotype":"protein_coding","ncbi_id":"3305","summary":"This gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein. [provided by RefSeq, Jul 2008]","start":31796990,"end":31802435,"strand":-1,"description":"heat shock protein family A (Hsp70) member 1 like [Source:HGNC Symbol;Acc:HGNC:5234]"}, {"versioned_ensembl_gene_id":"ENSG00000240395.1","gene_symbol":"RPL5P23","gene_name":"ribosomal protein L5 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36553]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270840","summary":null,"start":42341767,"end":42342634,"strand":-1,"description":"ribosomal protein L5 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:36553]"}, {"versioned_ensembl_gene_id":"ENSG00000235227.1","gene_symbol":"VN1R38P","gene_name":"vomeronasal 1 receptor 38 pseudogene [Source:HGNC Symbol;Acc:HGNC:37358]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100131065","summary":null,"start":64180006,"end":64180892,"strand":-1,"description":"vomeronasal 1 receptor 38 pseudogene [Source:HGNC Symbol;Acc:HGNC:37358]"}, {"versioned_ensembl_gene_id":"ENSG00000213644.2","gene_symbol":"SAPCD2P1","gene_name":"suppressor APC domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51277]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442320","summary":null,"start":64181710,"end":64182893,"strand":1,"description":"suppressor APC domain containing 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51277]"}, {"versioned_ensembl_gene_id":"ENSG00000254178.1","gene_symbol":"AC090103.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":25834129,"end":25840135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254560.5","gene_symbol":"BBOX1-AS1","gene_name":"BBOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50700]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"103695435","summary":null,"start":27047186,"end":27220113,"strand":-1,"description":"BBOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50700]"}, {"versioned_ensembl_gene_id":"ENSG00000015285.10","gene_symbol":"WAS","gene_name":"Wiskott-Aldrich syndrome [Source:HGNC Symbol;Acc:HGNC:12731]","synonyms":"WASP,THC,IMD2,WASPA","biotype":"protein_coding","ncbi_id":"7454","summary":" The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5' UTR sequence, has been described, however, its full-length nature is not known. [provided by RefSeq, Jul 2008]","start":48676596,"end":48691427,"strand":1,"description":"Wiskott-Aldrich syndrome [Source:HGNC Symbol;Acc:HGNC:12731]"}, {"versioned_ensembl_gene_id":"ENSG00000205763.13","gene_symbol":"RP9P","gene_name":"retinitis pigmentosa 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33969]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"441212","summary":null,"start":32916815,"end":32943176,"strand":-1,"description":"retinitis pigmentosa 9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33969]"}, {"versioned_ensembl_gene_id":"ENSG00000118702.9","gene_symbol":"GHRH","gene_name":"growth hormone releasing hormone [Source:HGNC Symbol;Acc:HGNC:4265]","synonyms":"GHRF","biotype":"protein_coding","ncbi_id":"2691","summary":"This gene encodes a member of the glucagon family of proteins. The encoded preproprotein is produced in the hypothalamus and cleaved to generate the mature factor, known as somatoliberin, which acts to stimulate growth hormone release from the pituitary gland. Variant receptors for somatoliberin have been found in several types of tumors, and antagonists of these receptors can inhibit the growth of the tumors. Defects in this gene are a cause of dwarfism, while hypersecretion of the encoded protein is a cause of gigantism. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]","start":37251082,"end":37261835,"strand":-1,"description":"growth hormone releasing hormone [Source:HGNC Symbol;Acc:HGNC:4265]"}, {"versioned_ensembl_gene_id":"ENSG00000101843.18","gene_symbol":"PSMD10","gene_name":"proteasome 26S subunit, non-ATPase 10 [Source:HGNC Symbol;Acc:HGNC:9555]","synonyms":"p28","biotype":"protein_coding","ncbi_id":"5716","summary":"This gene encodes a subunit of the PA700/19S complex, which is the regulatory component of the 26S proteasome. The 26S proteosome complex is required for ubiquitin-dependent protein degradation. This protein is a non-ATPase subunit that may be involved in protein-protein interactions. Aberrant expression of this gene may paly a role in tumorigenesis. Two transcripts encoding different isoforms have been described. Pseudogenes have been identified on chromosomes 3 and 20.[provided by RefSeq, Mar 2011]","start":108084207,"end":108091618,"strand":-1,"description":"proteasome 26S subunit, non-ATPase 10 [Source:HGNC Symbol;Acc:HGNC:9555]"}, {"versioned_ensembl_gene_id":"ENSG00000197465.13","gene_symbol":"GYPE","gene_name":"glycophorin E (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4705]","synonyms":"MNS,GPE","biotype":"protein_coding","ncbi_id":"2996","summary":"The protein encoded by this gene is a sialoglycoprotein and a type I membrane protein. It is a member of a gene family with GPA and GPB genes. This encoded protein might carry the M blood group antigen. GYPA, GYPB, and GYPE are organized in tandem on chromosome 4. This gene might have derived from an ancestral gene common to the GPB gene by gene duplication. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]","start":143870867,"end":143905563,"strand":-1,"description":"glycophorin E (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4705]"}, {"versioned_ensembl_gene_id":"ENSG00000174898.15","gene_symbol":"CATSPERD","gene_name":"cation channel sperm associated auxiliary subunit delta [Source:HGNC Symbol;Acc:HGNC:28598]","synonyms":"TMEM146,MGC39581","biotype":"protein_coding","ncbi_id":"257062","summary":null,"start":5720677,"end":5778734,"strand":1,"description":"cation channel sperm associated auxiliary subunit delta [Source:HGNC Symbol;Acc:HGNC:28598]"}, {"versioned_ensembl_gene_id":"ENSG00000104921.14","gene_symbol":"FCER2","gene_name":"Fc fragment of IgE receptor II [Source:HGNC Symbol;Acc:HGNC:3612]","synonyms":"FCE2,CLEC4J,CD23A,CD23","biotype":"protein_coding","ncbi_id":"2208","summary":"The protein encoded by this gene is a B-cell specific antigen, and a low-affinity receptor for IgE. It has essential roles in B cell growth and differentiation, and the regulation of IgE production. This protein also exists as a soluble secreted form, then functioning as a potent mitogenic growth factor. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]","start":7688758,"end":7702146,"strand":-1,"description":"Fc fragment of IgE receptor II [Source:HGNC Symbol;Acc:HGNC:3612]"}, {"versioned_ensembl_gene_id":"ENSG00000108452.1","gene_symbol":"ZNF29P","gene_name":"zinc finger protein 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:13080]","synonyms":"ZNF29,KOX26","biotype":"unprocessed_pseudogene","ncbi_id":"7577","summary":null,"start":15675476,"end":15675643,"strand":1,"description":"zinc finger protein 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:13080]"}, {"versioned_ensembl_gene_id":"ENSG00000223544.1","gene_symbol":"AC005838.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15588852,"end":15589084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251537.4","gene_symbol":"AC005324.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":15571491,"end":15651653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128284.19","gene_symbol":"APOL3","gene_name":"apolipoprotein L3 [Source:HGNC Symbol;Acc:HGNC:14868]","synonyms":"CG12-1,APOLIII","biotype":"protein_coding","ncbi_id":"80833","summary":"This gene is a member of the apolipoprotein L gene family, and it is present in a cluster with other family members on chromosome 22. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids, including cholesterol, and/or allow the binding of lipids to organelles. In addition, expression of this gene is up-regulated by tumor necrosis factor-alpha in endothelial cells lining the normal and atherosclerotic iliac artery and aorta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":36140330,"end":36166177,"strand":-1,"description":"apolipoprotein L3 [Source:HGNC Symbol;Acc:HGNC:14868]"}, {"versioned_ensembl_gene_id":"ENSG00000228371.1","gene_symbol":"ZDHHC20P1","gene_name":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]","synonyms":"OTTHUMG00000086707","biotype":"processed_pseudogene","ncbi_id":"100048907","summary":null,"start":29708017,"end":29708439,"strand":-1,"description":"zinc finger DHHC-type containing 20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33456]"}, {"versioned_ensembl_gene_id":"ENSG00000068308.13","gene_symbol":"OTUD5","gene_name":"OTU deubiquitinase 5 [Source:HGNC Symbol;Acc:HGNC:25402]","synonyms":"DUBA,DKFZp761A052","biotype":"protein_coding","ncbi_id":"55593","summary":"This gene encodes a member of the OTU (ovarian tumor) domain-containing cysteine protease superfamily. The OTU domain confers deubiquitinase activity and the encoded protein has been shown to suppress the type I interferon-dependent innate immune response by cleaving the polyubiquitin chain from an essential type I interferon adaptor protein. Cleavage results in disassociation of the adaptor protein from a downstream signaling complex and disruption of the type I interferon signaling cascade. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2008]","start":48922028,"end":48958386,"strand":-1,"description":"OTU deubiquitinase 5 [Source:HGNC Symbol;Acc:HGNC:25402]"}, {"versioned_ensembl_gene_id":"ENSG00000241322.10","gene_symbol":"CDRT1","gene_name":"CMT1A duplicated region transcript 1 [Source:HGNC Symbol;Acc:HGNC:14379]","synonyms":"FBXW10P1,FBXW10B,SM25H2,HREP","biotype":"protein_coding","ncbi_id":"374286","summary":"Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":15565483,"end":15619512,"strand":-1,"description":"CMT1A duplicated region transcript 1 [Source:HGNC Symbol;Acc:HGNC:14379]"}, {"versioned_ensembl_gene_id":"ENSG00000234684.6","gene_symbol":"SDCBP2-AS1","gene_name":"SDCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44314]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507495","summary":null,"start":1325405,"end":1378734,"strand":1,"description":"SDCBP2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44314]"}, {"versioned_ensembl_gene_id":"ENSG00000273973.1","gene_symbol":"AC025162.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":55929170,"end":55929729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242405.2","gene_symbol":"AC007537.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12155262,"end":12155772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130182.7","gene_symbol":"ZSCAN10","gene_name":"zinc finger and SCAN domain containing 10 [Source:HGNC Symbol;Acc:HGNC:12997]","synonyms":"ZNF206","biotype":"protein_coding","ncbi_id":"84891","summary":null,"start":3088890,"end":3099317,"strand":-1,"description":"zinc finger and SCAN domain containing 10 [Source:HGNC Symbol;Acc:HGNC:12997]"}, {"versioned_ensembl_gene_id":"ENSG00000070018.8","gene_symbol":"LRP6","gene_name":"LDL receptor related protein 6 [Source:HGNC Symbol;Acc:HGNC:6698]","synonyms":"ADCAD2","biotype":"protein_coding","ncbi_id":"4040","summary":"This gene encodes a member of the low density lipoprotein (LDL) receptor gene family. LDL receptors are transmembrane cell surface proteins involved in receptor-mediated endocytosis of lipoprotein and protein ligands. The protein encoded by this gene functions as a receptor or, with Frizzled, a co-receptor for Wnt and thereby transmits the canonical Wnt/beta-catenin signaling cascade. Through its interaction with the Wnt/beta-catenin signaling cascade this gene plays a role in the regulation of cell differentiation, proliferation, and migration and the development of many cancer types. This protein undergoes gamma-secretase dependent RIP- (regulated intramembrane proteolysis) processing but the precise locations of the cleavage sites have not been determined.[provided by RefSeq, Dec 2009]","start":12116025,"end":12267012,"strand":-1,"description":"LDL receptor related protein 6 [Source:HGNC Symbol;Acc:HGNC:6698]"}, {"versioned_ensembl_gene_id":"ENSG00000267699.2","gene_symbol":"AC091551.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":50968019,"end":51058144,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000108557.18","gene_symbol":"RAI1","gene_name":"retinoic acid induced 1 [Source:HGNC Symbol;Acc:HGNC:9834]","synonyms":"KIAA1820,DKFZP434A139,SMS,SMCR,MGC12824","biotype":"protein_coding","ncbi_id":"10743","summary":"This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]","start":17681473,"end":17811453,"strand":1,"description":"retinoic acid induced 1 [Source:HGNC Symbol;Acc:HGNC:9834]"}, {"versioned_ensembl_gene_id":"ENSG00000125879.4","gene_symbol":"OTOR","gene_name":"otoraplin [Source:HGNC Symbol;Acc:HGNC:8517]","synonyms":"MIAL1,MIAL,FDP","biotype":"protein_coding","ncbi_id":"56914","summary":"This gene encodes a member of the melanoma-inhibiting activity gene family. The encoded protein is secreted via the Golgi apparatus and may function in cartilage development and maintenance. A frequent polymorphism in the translation start codon of this gene can abolish translation and may be associated with forms of deafness. [provided by RefSeq, Jul 2013]","start":16748358,"end":16770062,"strand":1,"description":"otoraplin [Source:HGNC Symbol;Acc:HGNC:8517]"}, {"versioned_ensembl_gene_id":"ENSG00000281900.1","gene_symbol":"AP000350.15","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23926900,"end":23929574,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281111.1","gene_symbol":"AC130310.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1659817,"end":1660576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186572.2","gene_symbol":"DEFB107A","gene_name":"defensin beta 107A [Source:HGNC Symbol;Acc:HGNC:18086]","synonyms":"DEFB107,DEFB-7","biotype":"protein_coding","ncbi_id":"245910","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 107, DEFB107A and DEFB107B, in tail-to-tail orientation. This gene, DEFB107A, represents the more centromeric copy. [provided by RefSeq, Oct 2014]","start":7811720,"end":7815716,"strand":-1,"description":"defensin beta 107A [Source:HGNC Symbol;Acc:HGNC:18086]"}, {"versioned_ensembl_gene_id":"ENSG00000255608.1","gene_symbol":"AC006063.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4838955,"end":4842675,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170473.16","gene_symbol":"PYM1","gene_name":"PYM homolog 1, exon junction complex associated factor [Source:HGNC Symbol;Acc:HGNC:30258]","synonyms":"WIBG,PYM","biotype":"protein_coding","ncbi_id":"84305","summary":null,"start":55901413,"end":55932618,"strand":-1,"description":"PYM homolog 1, exon junction complex associated factor [Source:HGNC Symbol;Acc:HGNC:30258]"}, {"versioned_ensembl_gene_id":"ENSG00000224610.1","gene_symbol":"AC108879.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39226103,"end":39299786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256988.1","gene_symbol":"AC005833.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4806542,"end":4808641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255474.1","gene_symbol":"AC005833.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4700417,"end":4720102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255639.2","gene_symbol":"AC005833.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4657634,"end":4744581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270447.1","gene_symbol":"AC007179.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59514890,"end":59515124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164162.13","gene_symbol":"ANAPC10","gene_name":"anaphase promoting complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:24077]","synonyms":"DOC1,DKFZP564L0562,APC10","biotype":"protein_coding","ncbi_id":"10393","summary":"ANAPC10 is a core subunit of the anaphase-promoting complex (APC), or cyclosome, a ubiquitin protein ligase that is essential for progression through the cell cycle. APC initiates sister chromatid separation by ubiquitinating the anaphase inhibitor securin (PTTG1; MIM 604147) and triggers exit from mitosis by ubiquitinating cyclin B (CCNB1; MIM 123836), the activating subunit of cyclin-dependent kinase-1 (CDK1; MIM 116940) (summary by Wendt et al., 2001 [PubMed 11524682]).[supplied by OMIM, Feb 2011]","start":144831908,"end":145098541,"strand":-1,"description":"anaphase promoting complex subunit 10 [Source:HGNC Symbol;Acc:HGNC:24077]"}, {"versioned_ensembl_gene_id":"ENSG00000254778.7","gene_symbol":"AL662828.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32102303,"end":32120449,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235304.1","gene_symbol":"LINC01281","gene_name":"long intergenic non-protein coding RNA 1281 [Source:HGNC Symbol;Acc:HGNC:50337]","synonyms":null,"biotype":"lincRNA","ncbi_id":"286442","summary":null,"start":39304956,"end":39327362,"strand":-1,"description":"long intergenic non-protein coding RNA 1281 [Source:HGNC Symbol;Acc:HGNC:50337]"}, {"versioned_ensembl_gene_id":"ENSG00000233891.7","gene_symbol":"AC007179.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59238714,"end":59733396,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141642.8","gene_symbol":"ELAC1","gene_name":"elaC ribonuclease Z 1 [Source:HGNC Symbol;Acc:HGNC:14197]","synonyms":"D29","biotype":"protein_coding","ncbi_id":"55520","summary":null,"start":50967991,"end":50988121,"strand":1,"description":"elaC ribonuclease Z 1 [Source:HGNC Symbol;Acc:HGNC:14197]"}, {"versioned_ensembl_gene_id":"ENSG00000274322.1","gene_symbol":"AL136531.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1317571,"end":1393096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256381.1","gene_symbol":"AC005832.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":4645496,"end":4648027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236747.1","gene_symbol":"LINC01282","gene_name":"long intergenic non-protein coding RNA 1282 [Source:HGNC Symbol;Acc:HGNC:50338]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927449","summary":null,"start":39367285,"end":39391774,"strand":-1,"description":"long intergenic non-protein coding RNA 1282 [Source:HGNC Symbol;Acc:HGNC:50338]"}, {"versioned_ensembl_gene_id":"ENSG00000129810.14","gene_symbol":"SGO1","gene_name":"shugoshin 1 [Source:HGNC Symbol;Acc:HGNC:25088]","synonyms":"SGOL1,NY-BR-85","biotype":"protein_coding","ncbi_id":"151648","summary":"The protein encoded by this gene is a member of the shugoshin family of proteins. This protein is thought to protect centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression of this gene leads to the premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest. Evidence suggests that this protein also protects a small subset of cohesin found along the length of the chromosome arms during mitotic prophase. An isoform lacking exon 6 has been shown to play a role in the cohesion of centrioles (PMID: 16582621 and PMID:18331714). Mutations in this gene have been associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by the co-occurrence of Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO) within the first four decades of life (PMID:25282101). Fibroblast cells from CAID patients exhibited both increased cell proliferation and higher rates of senescence. Pseudogenes of this gene have been found on chromosomes 1 and 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]","start":20160593,"end":20186292,"strand":-1,"description":"shugoshin 1 [Source:HGNC Symbol;Acc:HGNC:25088]"}, {"versioned_ensembl_gene_id":"ENSG00000130035.6","gene_symbol":"GALNT8","gene_name":"polypeptide N-acetylgalactosaminyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:4130]","synonyms":"GALNAC-T8","biotype":"protein_coding","ncbi_id":"26290","summary":"This gene encodes a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes. GalNAc-Ts initiate mucin-type O-linked glycosylation in the Golgi apparatus by catalyzing the transfer of GalNAc to serine and threonine residues on target proteins. They are characterized by an N-terminal transmembrane domain, a stem region, a lumenal catalytic domain containing a GT1 motif and Gal/GalNAc transferase motif, and a C-terminal ricin/lectin-like domain. GalNAc-Ts have different, but overlapping, substrate specificities and patterns of expression. [provided by RefSeq, Jul 2008]","start":4720341,"end":4851927,"strand":1,"description":"polypeptide N-acetylgalactosaminyltransferase 8 [Source:HGNC Symbol;Acc:HGNC:4130]"}, {"versioned_ensembl_gene_id":"ENSG00000273651.4","gene_symbol":"GOLGA8G","gene_name":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]","synonyms":"DKFZp434K052","biotype":"protein_coding","ncbi_id":"283768","summary":null,"start":28531231,"end":28544591,"strand":-1,"description":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]"}, {"versioned_ensembl_gene_id":"ENSG00000213719.8","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31730581,"end":31739763,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000234191.1","gene_symbol":"AC091808.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39401252,"end":39434824,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280162.1","gene_symbol":"AL136531.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":1320710,"end":1324367,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272695.1","gene_symbol":"GAS6-AS2","gene_name":"GAS6 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43694]","synonyms":"FLJ44054","biotype":"lincRNA","ncbi_id":"100506394","summary":null,"start":113864168,"end":113866833,"strand":1,"description":"GAS6 antisense RNA 2 (head to head) [Source:HGNC Symbol;Acc:HGNC:43694]"}, {"versioned_ensembl_gene_id":"ENSG00000223383.1","gene_symbol":"HIST1H2APS6","gene_name":"histone cluster 1 H2A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42647]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100509927","summary":"Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is a histone pseudogene found on chromosome 13. [provided by RefSeq, Oct 2015]","start":36490078,"end":36490441,"strand":-1,"description":"histone cluster 1 H2A pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:42647]"}, {"versioned_ensembl_gene_id":"ENSG00000235056.1","gene_symbol":"AC010983.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195003711,"end":195026370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100030.14","gene_symbol":"MAPK1","gene_name":"mitogen-activated protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:6871]","synonyms":"PRKM1,p41mapk,MAPK2,ERK2,ERK,PRKM2","biotype":"protein_coding","ncbi_id":"5594","summary":"This gene encodes a member of the MAP kinase family. MAP kinases, also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. The activation of this kinase requires its phosphorylation by upstream kinases. Upon activation, this kinase translocates to the nucleus of the stimulated cells, where it phosphorylates nuclear targets. One study also suggests that this protein acts as a transcriptional repressor independent of its kinase activity. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Two alternatively spliced transcript variants encoding the same protein, but differing in the UTRs, have been reported for this gene. [provided by RefSeq, Jan 2014]","start":21754500,"end":21867680,"strand":-1,"description":"mitogen-activated protein kinase 1 [Source:HGNC Symbol;Acc:HGNC:6871]"}, {"versioned_ensembl_gene_id":"ENSG00000222030.1","gene_symbol":"LINC01793","gene_name":"long intergenic non-protein coding RNA 1793 [Source:HGNC Symbol;Acc:HGNC:52583]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927285","summary":null,"start":59217708,"end":59279400,"strand":1,"description":"long intergenic non-protein coding RNA 1793 [Source:HGNC Symbol;Acc:HGNC:52583]"}, {"versioned_ensembl_gene_id":"ENSG00000226746.2","gene_symbol":"SMCR5","gene_name":"Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17918]","synonyms":"NCRNA00034","biotype":"antisense_RNA","ncbi_id":"140771","summary":null,"start":17776686,"end":17779529,"strand":-1,"description":"Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:17918]"}, {"versioned_ensembl_gene_id":"ENSG00000237328.1","gene_symbol":"RAI1-AS1","gene_name":"RAI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40496]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861516","summary":null,"start":17759154,"end":17770821,"strand":-1,"description":"RAI1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40496]"}, {"versioned_ensembl_gene_id":"ENSG00000264167.1","gene_symbol":"AC122129.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17777781,"end":17779094,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166794.4","gene_symbol":"PPIB","gene_name":"peptidylprolyl isomerase B [Source:HGNC Symbol;Acc:HGNC:9255]","synonyms":"OI9,CYPB","biotype":"protein_coding","ncbi_id":"5479","summary":"The protein encoded by this gene is a cyclosporine-binding protein and is mainly located within the endoplasmic reticulum. It is associated with the secretory pathway and released in biological fluids. This protein can bind to cells derived from T- and B-lymphocytes, and may regulate cyclosporine A-mediated immunosuppression. Variants have been identified in this protein that give rise to recessive forms of osteogenesis imperfecta. [provided by RefSeq, Oct 2009]","start":64155812,"end":64163205,"strand":-1,"description":"peptidylprolyl isomerase B [Source:HGNC Symbol;Acc:HGNC:9255]"}, {"versioned_ensembl_gene_id":"ENSG00000072310.16","gene_symbol":"SREBF1","gene_name":"sterol regulatory element binding transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:11289]","synonyms":"SREBP1a,SREBP1,SREBP-1c,bHLHd1","biotype":"protein_coding","ncbi_id":"6720","summary":"This gene encodes a basic helix-loop-helix-leucine zipper (bHLH-Zip) transcription factor that binds to the sterol regulatory element-1 (SRE1), which is a motif that is found in the promoter of the low density lipoprotein receptor gene and other genes involved in sterol biosynthesis. The encoded protein is synthesized as a precursor that is initially attached to the nuclear membrane and endoplasmic reticulum. Following cleavage, the mature protein translocates to the nucleus and activates transcription. This cleaveage is inhibited by sterols. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative promoter usage and splicing result in multiple transcript variants, including SREBP-1a and SREBP-1c, which correspond to RefSeq transcript variants 2 and 3, respectively. [provided by RefSeq, Nov 2017]","start":17810399,"end":17837002,"strand":-1,"description":"sterol regulatory element binding transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:11289]"}, {"versioned_ensembl_gene_id":"ENSG00000278288.4","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707923,"end":54713345,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000229600.1","gene_symbol":"AL391336.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93886900,"end":93889410,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206256.14","gene_symbol":"PPT2","gene_name":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9374","summary":"This gene encodes a member of the palmitoyl-protein thioesterase family. The encoded glycosylated lysosomal protein has palmitoyl-CoA hydrolase activity in vitro, but does not hydrolyze palmitate from cysteine residues in proteins. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream EGFL8 (EGF-like-domain, multiple 8) gene. [provided by RefSeq, Feb 2011]","start":32101899,"end":32112151,"strand":1,"description":"palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:HGNC:9326]"}, {"versioned_ensembl_gene_id":"ENSG00000231143.1","gene_symbol":"AL157378.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94163920,"end":94194658,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227066.1","gene_symbol":"Z98257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20154338,"end":20160568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220370.1","gene_symbol":"AL078595.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94344737,"end":94344962,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261181.1","gene_symbol":"AC136619.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":16394912,"end":16398594,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279403.1","gene_symbol":"AL078595.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":94397664,"end":94398829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261362.1","gene_symbol":"AC136619.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16541217,"end":16541847,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278360.1","gene_symbol":"AC245128.15","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237724.5","gene_symbol":"HSPA1A","gene_name":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]","synonyms":"HSPA1,HSP70-1","biotype":"protein_coding","ncbi_id":"3303","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31802834,"end":31805316,"strand":1,"description":"heat shock protein family A (Hsp70) member 1A [Source:HGNC Symbol;Acc:HGNC:5232]"}, {"versioned_ensembl_gene_id":"ENSG00000260126.1","gene_symbol":"AC092326.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16658227,"end":16664135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197646.7","gene_symbol":"PDCD1LG2","gene_name":"programmed cell death 1 ligand 2 [Source:HGNC Symbol;Acc:HGNC:18731]","synonyms":"PD-L2,CD273,Btdc,bA574F11.2,B7-DC,PDL2","biotype":"protein_coding","ncbi_id":"80380","summary":null,"start":5510570,"end":5571254,"strand":1,"description":"programmed cell death 1 ligand 2 [Source:HGNC Symbol;Acc:HGNC:18731]"}, {"versioned_ensembl_gene_id":"ENSG00000106638.15","gene_symbol":"TBL2","gene_name":"transducin beta like 2 [Source:HGNC Symbol;Acc:HGNC:11586]","synonyms":"WS-betaTRP,WBSCR13,DKFZP43N024","biotype":"protein_coding","ncbi_id":"26608","summary":"This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008]","start":73568932,"end":73578791,"strand":-1,"description":"transducin beta like 2 [Source:HGNC Symbol;Acc:HGNC:11586]"}, {"versioned_ensembl_gene_id":"ENSG00000253719.3","gene_symbol":"ATXN7L3B","gene_name":"ataxin 7 like 3B [Source:HGNC Symbol;Acc:HGNC:37931]","synonyms":"lnc-SCA7","biotype":"protein_coding","ncbi_id":"552889","summary":null,"start":74537827,"end":74545430,"strand":1,"description":"ataxin 7 like 3B [Source:HGNC Symbol;Acc:HGNC:37931]"}, {"versioned_ensembl_gene_id":"ENSG00000233864.7","gene_symbol":"TTTY15","gene_name":"testis-specific transcript, Y-linked 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18567]","synonyms":"NCRNA00138,DKFZP434I143","biotype":"lincRNA","ncbi_id":"64595","summary":null,"start":12662334,"end":12692233,"strand":1,"description":"testis-specific transcript, Y-linked 15 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18567]"}, {"versioned_ensembl_gene_id":"ENSG00000153029.14","gene_symbol":"MR1","gene_name":"major histocompatibility complex, class I-related [Source:HGNC Symbol;Acc:HGNC:4975]","synonyms":"HLALS","biotype":"protein_coding","ncbi_id":"3140","summary":"MAIT (mucosal-associated invariant T-cells) lymphocytes represent a small population of T-cells primarily found in the gut. The protein encoded by this gene is an antigen-presenting molecule that presents metabolites of microbial vitamin B to MAITs. This presentation may activate the MAITs to regulate the amounts of specific types of bacteria in the gut. Several transcript variants encoding different isoforms have been found for this gene, and a pseudogene of it has been detected about 36 kbp upstream on the same chromosome. [provided by RefSeq, Jul 2015]","start":181033425,"end":181061938,"strand":1,"description":"major histocompatibility complex, class I-related [Source:HGNC Symbol;Acc:HGNC:4975]"}, {"versioned_ensembl_gene_id":"ENSG00000111254.7","gene_symbol":"AKAP3","gene_name":"A-kinase anchoring protein 3 [Source:HGNC Symbol;Acc:HGNC:373]","synonyms":"SOB1,FSP95,CT82,AKAP110","biotype":"protein_coding","ncbi_id":"10566","summary":"This gene encodes a member of A-kinase anchoring proteins (AKAPs), a family of functionally related proteins that target protein kinase A to discrete locations within the cell. The encoded protein is reported to participate in protein-protein interactions with the R-subunit of the protein kinase A as well as sperm-associated proteins. This protein is expressed in spermatozoa and localized to the acrosomal region of the sperm head as well as the length of the principal piece. It may function as a regulator of motility, capacitation, and the acrosome reaction. [provided by RefSeq, May 2013]","start":4615508,"end":4649047,"strand":-1,"description":"A-kinase anchoring protein 3 [Source:HGNC Symbol;Acc:HGNC:373]"}, {"versioned_ensembl_gene_id":"ENSG00000041357.15","gene_symbol":"PSMA4","gene_name":"proteasome subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:9533]","synonyms":"HsT17706,HC9","biotype":"protein_coding","ncbi_id":"5685","summary":"This gene encodes a core alpha subunit of the 20S proteosome, which is a highly ordered ring-shaped structure composed of four rings of 28 non-identical subunits. Proteasomes cleave peptides in an ATP- and ubiquitin-dependent manner. [provided by RefSeq, Aug 2016]","start":78540405,"end":78552419,"strand":1,"description":"proteasome subunit alpha 4 [Source:HGNC Symbol;Acc:HGNC:9533]"}, {"versioned_ensembl_gene_id":"ENSG00000257386.1","gene_symbol":"AC025257.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":74538145,"end":74538633,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224501.5","gene_symbol":"HSPA1B","gene_name":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]","synonyms":"HSP70-2","biotype":"protein_coding","ncbi_id":"3304","summary":"This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]","start":31815107,"end":31817630,"strand":1,"description":"heat shock protein family A (Hsp70) member 1B [Source:HGNC Symbol;Acc:HGNC:5233]"}, {"versioned_ensembl_gene_id":"ENSG00000279729.1","gene_symbol":"AC092326.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16760905,"end":16762465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103534.16","gene_symbol":"TMC5","gene_name":"transmembrane channel like 5 [Source:HGNC Symbol;Acc:HGNC:22999]","synonyms":"FLJ13593","biotype":"protein_coding","ncbi_id":"79838","summary":null,"start":19410496,"end":19499113,"strand":1,"description":"transmembrane channel like 5 [Source:HGNC Symbol;Acc:HGNC:22999]"}, {"versioned_ensembl_gene_id":"ENSG00000274545.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54700593,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000261748.1","gene_symbol":"AC098965.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":16952502,"end":16953468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257323.1","gene_symbol":"AC123904.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74656561,"end":74656860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235033.7","gene_symbol":"AL590999.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39881804,"end":39900071,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243317.7","gene_symbol":"C7orf73","gene_name":"chromosome 7 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:41909]","synonyms":"PL-5283","biotype":"protein_coding","ncbi_id":"647087","summary":null,"start":135662496,"end":135693418,"strand":1,"description":"chromosome 7 open reading frame 73 [Source:HGNC Symbol;Acc:HGNC:41909]"}, {"versioned_ensembl_gene_id":"ENSG00000157734.13","gene_symbol":"SNX22","gene_name":"sorting nexin 22 [Source:HGNC Symbol;Acc:HGNC:16315]","synonyms":"FLJ13952","biotype":"protein_coding","ncbi_id":"79856","summary":"The protein encoded by this gene is a sorting nexin that is found in the cytoplasm, where it interacts with membrane-bound phosphatidylinositol 3-phosphate. The encoded protein may play a role in intracellular trafficking. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012]","start":64151715,"end":64157481,"strand":1,"description":"sorting nexin 22 [Source:HGNC Symbol;Acc:HGNC:16315]"}, {"versioned_ensembl_gene_id":"ENSG00000279490.1","gene_symbol":"AC109446.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17082295,"end":17085049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104435.13","gene_symbol":"STMN2","gene_name":"stathmin 2 [Source:HGNC Symbol;Acc:HGNC:10577]","synonyms":"SCGN10,SCG10","biotype":"protein_coding","ncbi_id":"11075","summary":"This gene encodes a member of the stathmin family of phosphoproteins. Stathmin proteins function in microtubule dynamics and signal transduction. The encoded protein plays a regulatory role in neuronal growth and is also thought to be involved in osteogenesis. Reductions in the expression of this gene have been associated with Down's syndrome and Alzheimer's disease. Alternatively spliced transcript variants have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 6. [provided by RefSeq, Nov 2010]","start":79610814,"end":79666175,"strand":1,"description":"stathmin 2 [Source:HGNC Symbol;Acc:HGNC:10577]"}, {"versioned_ensembl_gene_id":"ENSG00000234225.2","gene_symbol":"AC244394.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":147001931,"end":147003618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146122.16","gene_symbol":"DAAM2","gene_name":"dishevelled associated activator of morphogenesis 2 [Source:HGNC Symbol;Acc:HGNC:18143]","synonyms":"KIAA0381","biotype":"protein_coding","ncbi_id":"23500","summary":null,"start":39792298,"end":39904877,"strand":1,"description":"dishevelled associated activator of morphogenesis 2 [Source:HGNC Symbol;Acc:HGNC:18143]"}, {"versioned_ensembl_gene_id":"ENSG00000065357.19","gene_symbol":"DGKA","gene_name":"diacylglycerol kinase alpha [Source:HGNC Symbol;Acc:HGNC:2849]","synonyms":"DGK-alpha,DAGK1,DAGK","biotype":"protein_coding","ncbi_id":"1606","summary":"The protein encoded by this gene belongs to the eukaryotic diacylglycerol kinase family. It acts as a modulator that competes with protein kinase C for the second messenger diacylglycerol in intracellular signaling pathways. It also plays an important role in the resynthesis of phosphatidylinositols and phosphorylating diacylglycerol to phosphatidic acid. Several transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Apr 2017]","start":55927319,"end":55954027,"strand":1,"description":"diacylglycerol kinase alpha [Source:HGNC Symbol;Acc:HGNC:2849]"}, {"versioned_ensembl_gene_id":"ENSG00000130300.8","gene_symbol":"PLVAP","gene_name":"plasmalemma vesicle associated protein [Source:HGNC Symbol;Acc:HGNC:13635]","synonyms":"PV1,PV-1,gp68,FELS","biotype":"protein_coding","ncbi_id":"83483","summary":null,"start":17351448,"end":17377350,"strand":-1,"description":"plasmalemma vesicle associated protein [Source:HGNC Symbol;Acc:HGNC:13635]"}, {"versioned_ensembl_gene_id":"ENSG00000166959.7","gene_symbol":"MS4A8","gene_name":"membrane spanning 4-domains A8 [Source:HGNC Symbol;Acc:HGNC:13380]","synonyms":"MS4A8B,MS4A4,CD20L5","biotype":"protein_coding","ncbi_id":"83661","summary":"This gene encodes a member of the membrane-spanning 4A gene family. Members of this protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. The gene encoding this protein is localized to 11q12.3, among a cluster of family members. [provided by RefSeq, Jul 2008]","start":60699574,"end":60715811,"strand":1,"description":"membrane spanning 4-domains A8 [Source:HGNC Symbol;Acc:HGNC:13380]"}, {"versioned_ensembl_gene_id":"ENSG00000164707.15","gene_symbol":"SLC13A4","gene_name":"solute carrier family 13 member 4 [Source:HGNC Symbol;Acc:HGNC:15827]","synonyms":"SUT1,SUT-1","biotype":"protein_coding","ncbi_id":"26266","summary":null,"start":135681237,"end":135729258,"strand":-1,"description":"solute carrier family 13 member 4 [Source:HGNC Symbol;Acc:HGNC:15827]"}, {"versioned_ensembl_gene_id":"ENSG00000278361.4","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850495,"end":54867253,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000230830.1","gene_symbol":"ARPP21-AS1","gene_name":"ARPP21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40785]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874098","summary":null,"start":35650197,"end":35651961,"strand":-1,"description":"ARPP21 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40785]"}, {"versioned_ensembl_gene_id":"ENSG00000137880.5","gene_symbol":"GCHFR","gene_name":"GTP cyclohydrolase I feedback regulator [Source:HGNC Symbol;Acc:HGNC:4194]","synonyms":"HsT16933,GFRP","biotype":"protein_coding","ncbi_id":"2644","summary":"GTP cyclohydrolase I feedback regulatory protein binds to and mediates tetrahydrobiopterin inhibition of GTP cyclohydrolase I. The regulatory protein, GCHFR, consists of a homodimer. It is postulated that GCHFR may play a role in regulating phenylalanine metabolism in the liver and in the production of biogenic amine neurotransmitters and nitric oxide. [provided by RefSeq, Jul 2008]","start":40764020,"end":40767710,"strand":1,"description":"GTP cyclohydrolase I feedback regulator [Source:HGNC Symbol;Acc:HGNC:4194]"}, {"versioned_ensembl_gene_id":"ENSG00000272921.1","gene_symbol":"AC005832.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4604944,"end":4662643,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172995.16","gene_symbol":"ARPP21","gene_name":"cAMP regulated phosphoprotein 21 [Source:HGNC Symbol;Acc:HGNC:16968]","synonyms":"TARPP,R3HDM3,ARPP-21","biotype":"protein_coding","ncbi_id":"10777","summary":"This gene encodes a cAMP-regulated phosphoprotein. The encoded protein is enriched in the caudate nucleus and cerebellar cortex. A similar protein in mouse may be involved in regulating the effects of dopamine in the basal ganglia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":35638945,"end":35794496,"strand":1,"description":"cAMP regulated phosphoprotein 21 [Source:HGNC Symbol;Acc:HGNC:16968]"}, {"versioned_ensembl_gene_id":"ENSG00000105298.13","gene_symbol":"CACTIN","gene_name":"cactin, spliceosome C complex subunit [Source:HGNC Symbol;Acc:HGNC:29938]","synonyms":"NY-REN-24,fSAPc,cactin,C19orf29","biotype":"protein_coding","ncbi_id":"58509","summary":null,"start":3610641,"end":3626815,"strand":-1,"description":"cactin, spliceosome C complex subunit [Source:HGNC Symbol;Acc:HGNC:29938]"}, {"versioned_ensembl_gene_id":"ENSG00000139180.10","gene_symbol":"NDUFA9","gene_name":"NADH:ubiquinone oxidoreductase subunit A9 [Source:HGNC Symbol;Acc:HGNC:7693]","synonyms":"SDR22E1,NDUFS2L,CI-39k","biotype":"protein_coding","ncbi_id":"4704","summary":"The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. A pseudogene has been identified on chromosome 12. [provided by RefSeq, May 2010]","start":4649095,"end":4694317,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A9 [Source:HGNC Symbol;Acc:HGNC:7693]"}, {"versioned_ensembl_gene_id":"ENSG00000228232.1","gene_symbol":"GAPDHP1","gene_name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4159]","synonyms":"GAPDP1,GAPDL2,GAPDHL2","biotype":"processed_pseudogene","ncbi_id":"2616","summary":null,"start":39787132,"end":39788136,"strand":-1,"description":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4159]"}, {"versioned_ensembl_gene_id":"ENSG00000230011.2","gene_symbol":"CTSLP4","gene_name":"cathepsin L pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23645]","synonyms":"OTTHUMG00000018237,CTSLL4,CTSL1P4,bA564C4.3","biotype":"unprocessed_pseudogene","ncbi_id":"644496","summary":null,"start":50705380,"end":50708906,"strand":-1,"description":"cathepsin L pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:23645]"}, {"versioned_ensembl_gene_id":"ENSG00000270759.1","gene_symbol":"AC091810.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39791580,"end":39791904,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261435.1","gene_symbol":"AL592164.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39837536,"end":39848358,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180440.3","gene_symbol":"SERTM1","gene_name":"serine rich and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33792]","synonyms":"C13orf36","biotype":"protein_coding","ncbi_id":"400120","summary":null,"start":36673912,"end":36697839,"strand":1,"description":"serine rich and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:33792]"}, {"versioned_ensembl_gene_id":"ENSG00000166140.17","gene_symbol":"ZFYVE19","gene_name":"zinc finger FYVE-type containing 19 [Source:HGNC Symbol;Acc:HGNC:20758]","synonyms":"FLJ14840,ANCHR","biotype":"protein_coding","ncbi_id":"84936","summary":null,"start":40807086,"end":40815084,"strand":1,"description":"zinc finger FYVE-type containing 19 [Source:HGNC Symbol;Acc:HGNC:20758]"}, {"versioned_ensembl_gene_id":"ENSG00000235306.2","gene_symbol":"GAPDHP34","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:37786]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646877","summary":null,"start":36740041,"end":36740863,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:37786]"}, {"versioned_ensembl_gene_id":"ENSG00000269350.1","gene_symbol":"AC010463.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17360932,"end":17362753,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198160.14","gene_symbol":"MIER1","gene_name":"MIER1 transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29657]","synonyms":"KIAA1610,hMI-ER1,MI-ER1","biotype":"protein_coding","ncbi_id":"57708","summary":"This gene encodes a protein that was first identified in Xenopus laevis by its role in a mesoderm induction early response (MIER). The encoded protein functions as a transcriptional regulator. Alternatively spliced transcript variants encode multiple isoforms, some of which lack a C-terminal nuclear localization signal. [provided by RefSeq, May 2013]","start":66924895,"end":66988619,"strand":1,"description":"MIER1 transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:29657]"}, {"versioned_ensembl_gene_id":"ENSG00000131370.15","gene_symbol":"SH3BP5","gene_name":"SH3 domain binding protein 5 [Source:HGNC Symbol;Acc:HGNC:10827]","synonyms":"Sab","biotype":"protein_coding","ncbi_id":"9467","summary":null,"start":15254853,"end":15341368,"strand":-1,"description":"SH3 domain binding protein 5 [Source:HGNC Symbol;Acc:HGNC:10827]"}, {"versioned_ensembl_gene_id":"ENSG00000223678.1","gene_symbol":"AL356218.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33402857,"end":33409948,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124574.14","gene_symbol":"ABCC10","gene_name":"ATP binding cassette subfamily C member 10 [Source:HGNC Symbol;Acc:HGNC:52]","synonyms":"SIMRP7,MRP7,EST182763","biotype":"protein_coding","ncbi_id":"89845","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This ABC full-transporter is a member of the MRP subfamily which is involved in multi-drug resistance. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2010]","start":43427366,"end":43450430,"strand":1,"description":"ATP binding cassette subfamily C member 10 [Source:HGNC Symbol;Acc:HGNC:52]"}, {"versioned_ensembl_gene_id":"ENSG00000140598.13","gene_symbol":"EFL1","gene_name":"elongation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:25789]","synonyms":"EFTUD1,RIA1,HsT19294,FLJ13119,FAM42A","biotype":"protein_coding","ncbi_id":"79631","summary":null,"start":82130230,"end":82262763,"strand":-1,"description":"elongation factor like GTPase 1 [Source:HGNC Symbol;Acc:HGNC:25789]"}, {"versioned_ensembl_gene_id":"ENSG00000181284.2","gene_symbol":"TMEM102","gene_name":"transmembrane protein 102 [Source:HGNC Symbol;Acc:HGNC:26722]","synonyms":"CBAP,FLJ36878","biotype":"protein_coding","ncbi_id":"284114","summary":null,"start":7435443,"end":7437679,"strand":1,"description":"transmembrane protein 102 [Source:HGNC Symbol;Acc:HGNC:26722]"}, {"versioned_ensembl_gene_id":"ENSG00000094963.13","gene_symbol":"FMO2","gene_name":"flavin containing monooxygenase 2 [Source:HGNC Symbol;Acc:HGNC:3770]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2327","summary":"This gene encodes a flavin-containing monooxygenase family member. It is an NADPH-dependent enzyme that catalyzes the N-oxidation of some primary alkylamines through an N-hydroxylamine intermediate. However, some human populations contain an allele (FMO2*2A) with a premature stop codon, resulting in a protein that is C-terminally-truncated, has no catalytic activity, and is likely degraded rapidly. This gene is found in a cluster with other related family members on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]","start":171185208,"end":171211230,"strand":1,"description":"flavin containing monooxygenase 2 [Source:HGNC Symbol;Acc:HGNC:3770]"}, {"versioned_ensembl_gene_id":"ENSG00000165272.14","gene_symbol":"AQP3","gene_name":"aquaporin 3 (Gill blood group) [Source:HGNC Symbol;Acc:HGNC:636]","synonyms":"GIL","biotype":"protein_coding","ncbi_id":"360","summary":"This gene encodes the water channel protein aquaporin 3. Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein, also known as aquaporin 0. Aquaporin 3 is localized at the basal lateral membranes of collecting duct cells in the kidney. In addition to its water channel function, aquaporin 3 has been found to facilitate the transport of nonionic small solutes such as urea and glycerol, but to a smaller degree. It has been suggested that water channels can be functionally heterogeneous and possess water and solute permeation mechanisms. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":33441154,"end":33447611,"strand":-1,"description":"aquaporin 3 (Gill blood group) [Source:HGNC Symbol;Acc:HGNC:636]"}, {"versioned_ensembl_gene_id":"ENSG00000139219.17","gene_symbol":"COL2A1","gene_name":"collagen type II alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2200]","synonyms":"STL1,SEDC,AOM","biotype":"protein_coding","ncbi_id":"1280","summary":"This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008]","start":47972965,"end":48004486,"strand":-1,"description":"collagen type II alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2200]"}, {"versioned_ensembl_gene_id":"ENSG00000270857.1","gene_symbol":"AC007621.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12248991,"end":12249427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186562.7","gene_symbol":"DEFB105A","gene_name":"defensin beta 105A [Source:HGNC Symbol;Acc:HGNC:18087]","synonyms":"DEFB105,DEFB-5","biotype":"protein_coding","ncbi_id":"245908","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 105, DEFB105A and DEFB105B, in tail-to-tail orientation. This gene, DEFB105A, represents the more centromeric copy. [provided by RefSeq, Oct 2014]","start":7821966,"end":7823889,"strand":-1,"description":"defensin beta 105A [Source:HGNC Symbol;Acc:HGNC:18087]"}, {"versioned_ensembl_gene_id":"ENSG00000121380.12","gene_symbol":"BCL2L14","gene_name":"BCL2 like 14 [Source:HGNC Symbol;Acc:HGNC:16657]","synonyms":"BCL-G,BCLG","biotype":"protein_coding","ncbi_id":"79370","summary":"The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. Overexpression of this gene has been shown to induce apoptosis in cells. Three alternatively spliced transcript variants encoding two distinct isoforms have been reported for this gene. [provided by RefSeq, May 2009]","start":12049844,"end":12211084,"strand":1,"description":"BCL2 like 14 [Source:HGNC Symbol;Acc:HGNC:16657]"}, {"versioned_ensembl_gene_id":"ENSG00000270484.1","gene_symbol":"AL078595.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94442030,"end":94443809,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189320.8","gene_symbol":"FAM180A","gene_name":"family with sequence similarity 180 member A [Source:HGNC Symbol;Acc:HGNC:33773]","synonyms":"UNQ1940,HWKM1940","biotype":"protein_coding","ncbi_id":"389558","summary":null,"start":135728348,"end":135748846,"strand":-1,"description":"family with sequence similarity 180 member A [Source:HGNC Symbol;Acc:HGNC:33773]"}, {"versioned_ensembl_gene_id":"ENSG00000216853.1","gene_symbol":"MTCYBP36","gene_name":"mitochondrially encoded cytochrome b pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:52304]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729116","summary":null,"start":94446740,"end":94447179,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 36 [Source:HGNC Symbol;Acc:HGNC:52304]"}, {"versioned_ensembl_gene_id":"ENSG00000231509.1","gene_symbol":"AL162253.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5584490,"end":5588994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219627.1","gene_symbol":"CYCSP17","gene_name":"cytochrome c, somatic pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:24390]","synonyms":"HCP17","biotype":"processed_pseudogene","ncbi_id":"360172","summary":null,"start":95504182,"end":95504496,"strand":1,"description":"cytochrome c, somatic pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:24390]"}, {"versioned_ensembl_gene_id":"ENSG00000228949.1","gene_symbol":"UGT1A12P","gene_name":"UDP glucuronosyltransferase family 1 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:12533]","synonyms":"UGT1L","biotype":"unprocessed_pseudogene","ncbi_id":"54573","summary":null,"start":233585439,"end":233586291,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:12533]"}, {"versioned_ensembl_gene_id":"ENSG00000227447.1","gene_symbol":"XGY1","gene_name":"Xg pseudogene, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:12807]","synonyms":"XGPY1,XGPY","biotype":"unprocessed_pseudogene","ncbi_id":"7500","summary":null,"start":12440046,"end":12507369,"strand":-1,"description":"Xg pseudogene, Y-linked 1 [Source:HGNC Symbol;Acc:HGNC:12807]"}, {"versioned_ensembl_gene_id":"ENSG00000226863.1","gene_symbol":"SHROOM2P1","gene_name":"shroom family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:631]","synonyms":"APXLP","biotype":"unprocessed_pseudogene","ncbi_id":"10031","summary":null,"start":12537773,"end":12544883,"strand":1,"description":"shroom family member 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:631]"}, {"versioned_ensembl_gene_id":"ENSG00000233774.1","gene_symbol":"MED14P1","gene_name":"mediator complex subunit 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2371]","synonyms":"MED14P,CXorf4P,CRSP2P","biotype":"unprocessed_pseudogene","ncbi_id":"359791","summary":null,"start":12618983,"end":12634402,"strand":-1,"description":"mediator complex subunit 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2371]"}, {"versioned_ensembl_gene_id":"ENSG00000281582.1","gene_symbol":"AP000350.14","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23901432,"end":23907068,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186579.2","gene_symbol":"DEFB106A","gene_name":"defensin beta 106A [Source:HGNC Symbol;Acc:HGNC:18088]","synonyms":"DEFB106,DEFB-6","biotype":"protein_coding","ncbi_id":"245909","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 106, DEFB106A and DEFB106B, in head-to-head orientation. This gene, DEFB106A, represents the more centromeric copy. [provided by RefSeq, Oct 2014]","start":7825172,"end":7829053,"strand":1,"description":"defensin beta 106A [Source:HGNC Symbol;Acc:HGNC:18088]"}, {"versioned_ensembl_gene_id":"ENSG00000273219.1","gene_symbol":"AC091736.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135704537,"end":135704841,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187566.5","gene_symbol":"NHLRC1","gene_name":"NHL repeat containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21576]","synonyms":"malin,EPM2B,bA204B7.2","biotype":"protein_coding","ncbi_id":"378884","summary":"The protein encoded by this gene is a single subunit E3 ubiquitin ligase. Laforin is polyubiquitinated by the encoded protein. Defects in this intronless gene lead to an accumulation of laforin and onset of Lafora disease, also known as progressive myoclonic epilepsy type 2 (EPM2).[provided by RefSeq, Mar 2010]","start":18120440,"end":18122687,"strand":-1,"description":"NHL repeat containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:21576]"}, {"versioned_ensembl_gene_id":"ENSG00000225243.5","gene_symbol":"AL021026.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":171199244,"end":171227788,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170175.10","gene_symbol":"CHRNB1","gene_name":"cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961]","synonyms":"CHRNB","biotype":"protein_coding","ncbi_id":"1140","summary":"The muscle acetylcholine receptor is composed of five subunits: two alpha subunits and one beta, one gamma, and one delta subunit. This gene encodes the beta subunit of the acetylcholine receptor. The acetylcholine receptor changes conformation upon acetylcholine binding leading to the opening of an ion-conducting channel across the plasma membrane. Mutations in this gene are associated with slow-channel congenital myasthenic syndrome. [provided by RefSeq, Jul 2008]","start":7445061,"end":7457707,"strand":1,"description":"cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961]"}, {"versioned_ensembl_gene_id":"ENSG00000281065.1","gene_symbol":"AP000350.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23939998,"end":23942798,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226800.5","gene_symbol":"CACTIN-AS1","gene_name":"CACTIN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31391]","synonyms":"C19orf29OS,C19orf29-AS1","biotype":"antisense_RNA","ncbi_id":"404665","summary":null,"start":3607247,"end":3613930,"strand":1,"description":"CACTIN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:31391]"}, {"versioned_ensembl_gene_id":"ENSG00000176782.2","gene_symbol":"DEFB104A","gene_name":"defensin beta 104A [Source:HGNC Symbol;Acc:HGNC:18115]","synonyms":"DEFB4,DEFB104,DEFB-4","biotype":"protein_coding","ncbi_id":"140596","summary":"Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 104, DEFB104A and DEFB104B, in head-to-head orientation. This gene, DEFB104A, represents the more centromeric copy. [provided by RefSeq, Oct 2014]","start":7836471,"end":7841242,"strand":1,"description":"defensin beta 104A [Source:HGNC Symbol;Acc:HGNC:18115]"}, {"versioned_ensembl_gene_id":"ENSG00000257119.1","gene_symbol":"EEF1B2P4","gene_name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32475]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130631","summary":null,"start":106901283,"end":106901984,"strand":-1,"description":"eukaryotic translation elongation factor 1 beta 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32475]"}, {"versioned_ensembl_gene_id":"ENSG00000225603.3","gene_symbol":"AC244394.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147050817,"end":147052481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188646.6","gene_symbol":"AC123904.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74663774,"end":74664141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227242.4","gene_symbol":"NBPF13P","gene_name":"NBPF member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:31995]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"644861","summary":"This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013]","start":147019656,"end":147056593,"strand":-1,"description":"NBPF member 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:31995]"}, {"versioned_ensembl_gene_id":"ENSG00000260675.1","gene_symbol":"AC109446.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":17094351,"end":17094927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280601.1","gene_symbol":"AP000350.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23949918,"end":23954042,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240631.1","gene_symbol":"RPL30P12","gene_name":"ribosomal protein L30 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36909]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271304","summary":null,"start":106910757,"end":106911109,"strand":1,"description":"ribosomal protein L30 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:36909]"}, {"versioned_ensembl_gene_id":"ENSG00000164946.19","gene_symbol":"FREM1","gene_name":"FRAS1 related extracellular matrix 1 [Source:HGNC Symbol;Acc:HGNC:23399]","synonyms":"TILRR,FLJ25461,DKFZp686M16108,C9orf154,C9orf145,C9orf143","biotype":"protein_coding","ncbi_id":"158326","summary":"This gene encodes a basement membrane protein that may play a role in craniofacial and renal development. Mutations in this gene have been associated with bifid nose with or without anorectal and renal anomalies. Alternatively spliced transcript variants encoding different isoforms have been described. PubMed ID 19940113 describes one such variant that initiates transcription within a distinct, internal exon; the resulting shorter isoform (named Toll-like/interleukin-1 receptor regulator, TILRR) is suggested to be a co-receptor of the interleukin 1 receptor family and may regulate receptor function and Toll-like receptor/interleukin 1 receptor signal transduction, contributing to the control of inflammatory response activation. [provided by RefSeq, Apr 2011]","start":14734666,"end":14910995,"strand":-1,"description":"FRAS1 related extracellular matrix 1 [Source:HGNC Symbol;Acc:HGNC:23399]"}, {"versioned_ensembl_gene_id":"ENSG00000282667.1","gene_symbol":"PRSS3P2","gene_name":"protease, serine 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43788]","synonyms":"TRY6","biotype":"unprocessed_pseudogene","ncbi_id":"154754","summary":"Although this locus appears to encode a protein similar to trypsinogen, the locus is thought to be a transcribed pseudogene. ESTs support its transcription, but expression of its predicted protein has not been observed. Its predicted protein sequence differs significantly from the known functional trypsinogens, including a different amino acid at the conserved residue 122 which is important for autolysis. This pseudogene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. [provided by RefSeq, Jul 2008]","start":142811706,"end":142815230,"strand":1,"description":"protease, serine 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43788]"}, {"versioned_ensembl_gene_id":"ENSG00000257998.1","gene_symbol":"AC123904.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74728038,"end":74728851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260329.1","gene_symbol":"AC007541.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":106954029,"end":106955497,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260405.1","gene_symbol":"AC109446.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17096202,"end":17096421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137364.4","gene_symbol":"TPMT","gene_name":"thiopurine S-methyltransferase [Source:HGNC Symbol;Acc:HGNC:12014]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7172","summary":"This gene encodes the enzyme that metabolizes thiopurine drugs via S-adenosyl-L-methionine as the S-methyl donor and S-adenosyl-L-homocysteine as a byproduct. Thiopurine drugs such as 6-mercaptopurine are used as chemotherapeutic agents. Genetic polymorphisms that affect this enzymatic activity are correlated with variations in sensitivity and toxicity to such drugs within individuals, causing thiopurine S-methyltransferase deficiency. Related pseudogenes have been identified on chromosomes 3, 18 and X. [provided by RefSeq, Aug 2014]","start":18128311,"end":18155074,"strand":-1,"description":"thiopurine S-methyltransferase [Source:HGNC Symbol;Acc:HGNC:12014]"}, {"versioned_ensembl_gene_id":"ENSG00000281265.1","gene_symbol":"AP000350.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23963780,"end":23964374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214324.5","gene_symbol":"C3orf56","gene_name":"chromosome 3 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:32481]","synonyms":"FLJ40141","biotype":"protein_coding","ncbi_id":"285311","summary":null,"start":127193131,"end":127198185,"strand":1,"description":"chromosome 3 open reading frame 56 [Source:HGNC Symbol;Acc:HGNC:32481]"}, {"versioned_ensembl_gene_id":"ENSG00000151079.7","gene_symbol":"AC005833.1","gene_name":"Potassium voltage-gated channel subfamily A member 6 [Source:UniProtKB/Swiss-Prot;Acc:P17658]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":4809176,"end":4813412,"strand":1,"description":"Potassium voltage-gated channel subfamily A member 6 [Source:UniProtKB/Swiss-Prot;Acc:P17658]"}, {"versioned_ensembl_gene_id":"ENSG00000104129.9","gene_symbol":"DNAJC17","gene_name":"DnaJ heat shock protein family (Hsp40) member C17 [Source:HGNC Symbol;Acc:HGNC:25556]","synonyms":"FLJ10634","biotype":"protein_coding","ncbi_id":"55192","summary":null,"start":40765155,"end":40807478,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C17 [Source:HGNC Symbol;Acc:HGNC:25556]"}, {"versioned_ensembl_gene_id":"ENSG00000230308.10","gene_symbol":"TRIM39","gene_name":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]","synonyms":"RNF23","biotype":"protein_coding","ncbi_id":"56658","summary":"The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The function of this protein has not been identified. This gene lies within the major histocompatibility complex class I region on chromosome 6. Alternate splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":30390376,"end":30407632,"strand":1,"description":"tripartite motif containing 39 [Source:HGNC Symbol;Acc:HGNC:10065]"}, {"versioned_ensembl_gene_id":"ENSG00000256799.1","gene_symbol":"AC005832.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4635349,"end":4636140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000095637.21","gene_symbol":"SORBS1","gene_name":"sorbin and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14565]","synonyms":"FLJ12406,CAP,sh3p12,SH3D5,ponsin,KIAA1296","biotype":"protein_coding","ncbi_id":"10580","summary":"This gene encodes a CBL-associated protein which functions in the signaling and stimulation of insulin. Mutations in this gene may be associated with human disorders of insulin resistance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":95311771,"end":95561414,"strand":-1,"description":"sorbin and SH3 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:14565]"}, {"versioned_ensembl_gene_id":"ENSG00000213722.8","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31727038,"end":31730617,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000281969.1","gene_symbol":"AL592158.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":39818751,"end":39823227,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000134508.12","gene_symbol":"CABLES1","gene_name":"Cdk5 and Abl enzyme substrate 1 [Source:HGNC Symbol;Acc:HGNC:25097]","synonyms":"HsT2563,FLJ35924","biotype":"protein_coding","ncbi_id":"91768","summary":"This gene encodes a protein involved in regulation of the cell cycle through interactions with several cyclin-dependent kinases. One study (PMID: 16177568) reported aberrant splicing of transcripts from this gene which results in removal of the cyclin binding domain only in human cancer cells, and reduction in gene expression was shown in colorectal cancers (PMID: 17982127).Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":23134564,"end":23260467,"strand":1,"description":"Cdk5 and Abl enzyme substrate 1 [Source:HGNC Symbol;Acc:HGNC:25097]"}, {"versioned_ensembl_gene_id":"ENSG00000256748.1","gene_symbol":"AC005832.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":4601991,"end":4603420,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254584.1","gene_symbol":"AL035078.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32035981,"end":32041318,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124615.17","gene_symbol":"MOCS1","gene_name":"molybdenum cofactor synthesis 1 [Source:HGNC Symbol;Acc:HGNC:7190]","synonyms":"MOCOD","biotype":"protein_coding","ncbi_id":"4337","summary":"Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16. [provided by RefSeq, Nov 2017]","start":39899578,"end":39934551,"strand":-1,"description":"molybdenum cofactor synthesis 1 [Source:HGNC Symbol;Acc:HGNC:7190]"}, {"versioned_ensembl_gene_id":"ENSG00000010219.13","gene_symbol":"DYRK4","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 4 [Source:HGNC Symbol;Acc:HGNC:3095]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8798","summary":"This gene encodes an enzyme that belongs to a conserved family of serine/threonine protein kinases. Members of this dual specificity kinase family are thought to function in the regulation of cell differentiation and proliferation, survival, and in development. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Aug 2013]","start":4562204,"end":4615302,"strand":1,"description":"dual specificity tyrosine phosphorylation regulated kinase 4 [Source:HGNC Symbol;Acc:HGNC:3095]"}, {"versioned_ensembl_gene_id":"ENSG00000281880.1","gene_symbol":"PAUPAR","gene_name":"PAX6 upstream antisense RNA [Source:NCBI gene;Acc:103157000]","synonyms":null,"biotype":"lincRNA","ncbi_id":"103157000","summary":"This gene is thought to produce a functional long non-coding RNA. Knockdown of this transcript results in genome-wide changes in gene expression, particularly of cell cyle genes, indicating a role in regulating differentiation. This transcript may bind to the promoter region of target genes and may also interact with the transcription factor Pax6 (paired box 6). [provided by RefSeq, Feb 2015]","start":31826347,"end":31829311,"strand":1,"description":"PAX6 upstream antisense RNA [Source:NCBI gene;Acc:103157000]"}, {"versioned_ensembl_gene_id":"ENSG00000049449.8","gene_symbol":"RCN1","gene_name":"reticulocalbin 1 [Source:HGNC Symbol;Acc:HGNC:9934]","synonyms":"RCN,Rcal,PIG20,FLJ37041","biotype":"protein_coding","ncbi_id":"5954","summary":"Reticulocalbin 1 is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. High conservation of amino acid residues outside of these motifs, in comparison to mouse reticulocalbin, is consistent with a possible biochemical function besides that of calcium binding. In human endothelial and prostate cancer cell lines this protein localizes to the plasma membrane.[provided by RefSeq, Jan 2009]","start":31812391,"end":32105755,"strand":1,"description":"reticulocalbin 1 [Source:HGNC Symbol;Acc:HGNC:9934]"}, {"versioned_ensembl_gene_id":"ENSG00000277897.2","gene_symbol":"GSTT2","gene_name":"glutathione S-transferase theta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4642]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2953","summary":"The protein encoded by this gene, glutathione S-transferase (GST) theta 2 (GSTT2), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT2 and GSTT2B are nearly identical to each other, and share 55% amino acid identity with GSTT1. All three genes may play a role in human carcinogenesis. The GSTT2 gene is a pseudogene in some populations. [provided by RefSeq, Sep 2015]","start":23980152,"end":23983919,"strand":1,"description":"glutathione S-transferase theta 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:4642]"}, {"versioned_ensembl_gene_id":"ENSG00000166006.12","gene_symbol":"KCNC2","gene_name":"potassium voltage-gated channel subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:6234]","synonyms":"Kv3.2","biotype":"protein_coding","ncbi_id":"3747","summary":"The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies. Based on sequence similarity, this gene is similar to one of these subfamilies, namely the Shaw subfamily. The protein encoded by this gene belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":75040077,"end":75209868,"strand":-1,"description":"potassium voltage-gated channel subfamily C member 2 [Source:HGNC Symbol;Acc:HGNC:6234]"}, {"versioned_ensembl_gene_id":"ENSG00000197123.9","gene_symbol":"ZNF679","gene_name":"zinc finger protein 679 [Source:HGNC Symbol;Acc:HGNC:28650]","synonyms":"MGC42415","biotype":"protein_coding","ncbi_id":"168417","summary":null,"start":64228474,"end":64266931,"strand":1,"description":"zinc finger protein 679 [Source:HGNC Symbol;Acc:HGNC:28650]"}, {"versioned_ensembl_gene_id":"ENSG00000132970.12","gene_symbol":"WASF3","gene_name":"WAS protein family member 3 [Source:HGNC Symbol;Acc:HGNC:12734]","synonyms":"WAVE3,SCAR3,KIAA0900","biotype":"protein_coding","ncbi_id":"10810","summary":"This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. A pseudogene of this gene have been defined on chromosome 6. Alternative splicing results in multiple transcript variants [provided by RefSeq, May 2014]","start":26557703,"end":26688948,"strand":1,"description":"WAS protein family member 3 [Source:HGNC Symbol;Acc:HGNC:12734]"}, {"versioned_ensembl_gene_id":"ENSG00000124493.13","gene_symbol":"GRM4","gene_name":"glutamate metabotropic receptor 4 [Source:HGNC Symbol;Acc:HGNC:4596]","synonyms":"GPRC1D,MGLUR4,mGlu4","biotype":"protein_coding","ncbi_id":"2914","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5 and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]","start":34018645,"end":34155622,"strand":-1,"description":"glutamate metabotropic receptor 4 [Source:HGNC Symbol;Acc:HGNC:4596]"}, {"versioned_ensembl_gene_id":"ENSG00000171462.14","gene_symbol":"DLK2","gene_name":"delta like non-canonical Notch ligand 2 [Source:HGNC Symbol;Acc:HGNC:21113]","synonyms":"MGC2487,EGFL9","biotype":"protein_coding","ncbi_id":"65989","summary":null,"start":43450352,"end":43456632,"strand":-1,"description":"delta like non-canonical Notch ligand 2 [Source:HGNC Symbol;Acc:HGNC:21113]"}, {"versioned_ensembl_gene_id":"ENSG00000229985.2","gene_symbol":"AL590640.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27176751,"end":27177277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275758.2","gene_symbol":"DDTL","gene_name":"D-dopachrome tautomerase like [Source:HGNC Symbol;Acc:HGNC:33446]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100037417","summary":null,"start":23966902,"end":23972534,"strand":1,"description":"D-dopachrome tautomerase like [Source:HGNC Symbol;Acc:HGNC:33446]"}, {"versioned_ensembl_gene_id":"ENSG00000281400.1","gene_symbol":"AP000351.8","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":23969213,"end":23969875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275003.3","gene_symbol":"DDT","gene_name":"D-dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2732]","synonyms":"DDCT","biotype":"protein_coding","ncbi_id":"1652","summary":"D-dopachrome tautomerase converts D-dopachrome into 5,6-dihydroxyindole. The DDT gene is related to the migration inhibitory factor (MIF) in terms of sequence, enzyme activity, and gene structure. DDT and MIF are closely linked on chromosome 22. [provided by RefSeq, Jul 2008]","start":23971367,"end":23980473,"strand":-1,"description":"D-dopachrome tautomerase [Source:HGNC Symbol;Acc:HGNC:2732]"}, {"versioned_ensembl_gene_id":"ENSG00000184787.18","gene_symbol":"UBE2G2","gene_name":"ubiquitin conjugating enzyme E2 G2 [Source:HGNC Symbol;Acc:HGNC:12483]","synonyms":"UBC7","biotype":"protein_coding","ncbi_id":"7327","summary":"The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. The encoded protein shares 100% sequence identity with the mouse counterpart. This gene is ubiquitously expressed, with high expression seen in adult muscle. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":44768580,"end":44802019,"strand":-1,"description":"ubiquitin conjugating enzyme E2 G2 [Source:HGNC Symbol;Acc:HGNC:12483]"}, {"versioned_ensembl_gene_id":"ENSG00000130700.6","gene_symbol":"GATA5","gene_name":"GATA binding protein 5 [Source:HGNC Symbol;Acc:HGNC:15802]","synonyms":"GATAS,bB379O24.1","biotype":"protein_coding","ncbi_id":"140628","summary":"The protein encoded by this gene is a transcription factor that contains two GATA-type zinc fingers. The encoded protein is known to bind to hepatocyte nuclear factor-1alpha (HNF-1alpha), and this interaction is essential for cooperative activation of the intestinal lactase-phlorizin hydrolase promoter. In other organisms, similar proteins may be involved in the establishment of cardiac smooth muscle cell diversity. [provided by RefSeq, Jul 2008]","start":62463497,"end":62475970,"strand":-1,"description":"GATA binding protein 5 [Source:HGNC Symbol;Acc:HGNC:15802]"}, {"versioned_ensembl_gene_id":"ENSG00000234031.1","gene_symbol":"RPS3AP44","gene_name":"ribosomal protein S3a pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36761]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646527","summary":null,"start":26576886,"end":26577675,"strand":1,"description":"ribosomal protein S3a pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36761]"}, {"versioned_ensembl_gene_id":"ENSG00000237001.6","gene_symbol":"WASF3-AS1","gene_name":"WASF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39841]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874061","summary":null,"start":26606544,"end":26641364,"strand":-1,"description":"WASF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39841]"}, {"versioned_ensembl_gene_id":"ENSG00000235239.1","gene_symbol":"Z74696.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128127090,"end":128128212,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248698.6","gene_symbol":"LINC01085","gene_name":"long intergenic non-protein coding RNA 1085 [Source:HGNC Symbol;Acc:HGNC:27198]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"152742","summary":null,"start":14111968,"end":14140052,"strand":1,"description":"long intergenic non-protein coding RNA 1085 [Source:HGNC Symbol;Acc:HGNC:27198]"}, {"versioned_ensembl_gene_id":"ENSG00000236985.1","gene_symbol":"AL121892.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16857962,"end":16864148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220540.1","gene_symbol":"AL359511.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17188134,"end":17188344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279155.1","gene_symbol":"AC233300.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48939992,"end":48940808,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250361.7","gene_symbol":"GYPB","gene_name":"glycophorin B (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4703]","synonyms":"SS,MNS,GPB,CD235b","biotype":"protein_coding","ncbi_id":"2994","summary":"Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups. GYPB gene consists of 5 exons and has 97% sequence homology with GYPA from the 5' UTR to the coding sequence encoding the first 45 amino acids. In addition to the M or N and S or s antigens, that commonly occur in all populations, about 40 related variant phenotypes have been identified. These variants include all the variants of the Miltenberger complex and several isoforms of Sta; also, Dantu, Sat, He, Mg, and deletion variants Ena, S-s-U- and Mk. Most of the variants are the result of gene recombinations between GYPA and GYPB. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":143996104,"end":144019345,"strand":-1,"description":"glycophorin B (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4703]"}, {"versioned_ensembl_gene_id":"ENSG00000276747.1","gene_symbol":"PADI6","gene_name":"peptidyl arginine deiminase 6 [Source:HGNC Symbol;Acc:HGNC:20449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353238","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. This protein may play a role in cytoskeletal reorganization in the egg and in early embryo development. [provided by RefSeq, Sep 2012]","start":17372196,"end":17401699,"strand":1,"description":"peptidyl arginine deiminase 6 [Source:HGNC Symbol;Acc:HGNC:20449]"}, {"versioned_ensembl_gene_id":"ENSG00000229071.9","gene_symbol":"PRRT1","gene_name":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]","synonyms":"IFITMD7,C6orf31,NG5","biotype":"protein_coding","ncbi_id":"80863","summary":null,"start":32096815,"end":32102831,"strand":-1,"description":"proline rich transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:13943]"}, {"versioned_ensembl_gene_id":"ENSG00000278302.2","gene_symbol":"KRTAP5-5","gene_name":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]","synonyms":"KRTAP5.5,KRTAP5-11","biotype":"protein_coding","ncbi_id":"439915","summary":null,"start":1629984,"end":1630868,"strand":1,"description":"keratin associated protein 5-5 [Source:HGNC Symbol;Acc:HGNC:23601]"}, {"versioned_ensembl_gene_id":"ENSG00000267697.1","gene_symbol":"LUZP6","gene_name":"leucine zipper protein 6 [Source:HGNC Symbol;Acc:HGNC:33955]","synonyms":"MTPNUT,MPD6","biotype":"protein_coding","ncbi_id":"767558","summary":"A bi-cistronic transcript encodes the products of both the myotrophin and leucine zipper protein 6 genes, which are located on chromosome 7. A cryptic ORF at the 3' end of the myotrophin transcript uses a novel internal ribosome entry site and a non-AUG translation initiation codon to produce leucine zipper protein 6, a 6.4 kDa tumor antigen that is associated with myeloproliferative disease. [provided by RefSeq, Jul 2008]","start":135927274,"end":135927450,"strand":-1,"description":"leucine zipper protein 6 [Source:HGNC Symbol;Acc:HGNC:33955]"}, {"versioned_ensembl_gene_id":"ENSG00000251679.1","gene_symbol":"AC073848.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14134936,"end":14143592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224746.1","gene_symbol":"AC015987.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":135926455,"end":135932881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198134.3","gene_symbol":"AC007537.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12111163,"end":12111489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105887.10","gene_symbol":"MTPN","gene_name":"myotrophin [Source:HGNC Symbol;Acc:HGNC:15667]","synonyms":"V-1,MYOTROPHIN,GCDP","biotype":"protein_coding","ncbi_id":"136319","summary":"The transcript produced from this gene is bi-cistronic and can encode both myotrophin and leucine zipper protein 6. The myotrophin protein is associated with cardiac hypertrophy, where it is involved in the conversion of NFkappa B p50-p65 heterodimers to p50-p50 and p65-p65 homodimers. This protein also has a potential function in cerebellar morphogenesis, and it may be involved in the differentiation of cerebellar neurons, particularly of granule cells. A cryptic ORF at the 3' end of this transcript uses a novel internal ribosome entry site and a non-AUG translation initiation codon to produce leucine zipper protein 6, a 6.4 kDa tumor antigen that is associated with myeloproliferative disease. [provided by RefSeq, Jul 2008]","start":135926761,"end":135977353,"strand":-1,"description":"myotrophin [Source:HGNC Symbol;Acc:HGNC:15667]"}, {"versioned_ensembl_gene_id":"ENSG00000235735.1","gene_symbol":"RPL7AP72","gene_name":"ribosomal protein L7a pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:36442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270754","summary":null,"start":128313281,"end":128314048,"strand":1,"description":"ribosomal protein L7a pseudogene 72 [Source:HGNC Symbol;Acc:HGNC:36442]"}, {"versioned_ensembl_gene_id":"ENSG00000092847.11","gene_symbol":"AGO1","gene_name":"argonaute 1, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:3262]","synonyms":"hAGO1,EIF2C1","biotype":"protein_coding","ncbi_id":"26523","summary":"This gene encodes a member of the argonaute family of proteins, which associate with small RNAs and have important roles in RNA interference (RNAi) and RNA silencing. This protein binds to microRNAs (miRNAs) or small interfering RNAs (siRNAs) and represses translation of mRNAs that are complementary to them. It is also involved in transcriptional gene silencing (TGS) of promoter regions that are complementary to bound short antigene RNAs (agRNAs), as well as in the degradation of miRNA-bound mRNA targets. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target, and that its mRNA could give rise to an additional C-terminally extended isoform by use of an alternative in-frame translation termination codon. [provided by RefSeq, Nov 2015]","start":35869808,"end":35930528,"strand":1,"description":"argonaute 1, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:3262]"}, {"versioned_ensembl_gene_id":"ENSG00000281722.1","gene_symbol":"AP000351.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23976905,"end":23977589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225689.1","gene_symbol":"AL442647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":128323620,"end":128600468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282565.1","gene_symbol":"AC239618.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":142821798,"end":142825331,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226802.1","gene_symbol":"AL442647.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":128440929,"end":128441785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259304.1","gene_symbol":"AC090888.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":44970035,"end":44971178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103037.11","gene_symbol":"SETD6","gene_name":"SET domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26116]","synonyms":"FLJ21148","biotype":"protein_coding","ncbi_id":"79918","summary":"This gene encodes a methyltransferase that adds a methyl group to the histone H2AZ, which is involved in nuclear receptor-dependent transcription. The protein also interacts with several endogenous proteins which are involved in nuclear hormone receptor signaling. A related pseudogene is located on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":58515479,"end":58521181,"strand":1,"description":"SET domain containing 6 [Source:HGNC Symbol;Acc:HGNC:26116]"}, {"versioned_ensembl_gene_id":"ENSG00000274741.1","gene_symbol":"AC138827.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70221290,"end":70240276,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224660.1","gene_symbol":"SH3BP5-AS1","gene_name":"SH3BP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44501]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100505696","summary":null,"start":15254184,"end":15264493,"strand":1,"description":"SH3BP5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44501]"}, {"versioned_ensembl_gene_id":"ENSG00000167014.10","gene_symbol":"TERB2","gene_name":"telomere repeat binding bouquet formation protein 2 [Source:HGNC Symbol;Acc:HGNC:28520]","synonyms":"MGC33951,C15orf43","biotype":"protein_coding","ncbi_id":"145645","summary":null,"start":44956702,"end":44979229,"strand":1,"description":"telomere repeat binding bouquet formation protein 2 [Source:HGNC Symbol;Acc:HGNC:28520]"}, {"versioned_ensembl_gene_id":"ENSG00000246575.2","gene_symbol":"AC093162.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":85315041,"end":85316529,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282049.1","gene_symbol":"PRSS2","gene_name":"protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:9483]","synonyms":"TRY2","biotype":"protein_coding","ncbi_id":"5645","summary":"This gene belongs to the trypsin family of serine proteases and encodes anionic trypsinogen. It is part of a cluster of trypsinogen genes that are located within the T cell receptor beta locus. Enzymes of this family cleave peptide bonds that follow lysine or arginine residues. This protein is found at high levels in pancreatic juice and its upregulation is a characteristic feature of pancreatitis. This protein has also been found to activate pro-urokinase in ovarian tumors, suggesting a function in tumor invasion. In addition, this enzyme is able to cleave across the type II collagen triple helix in rheumatoid arthritis synovitis tissue, potentially participating in the degradation of type II collagen-rich cartilage matrix. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2015]","start":142832063,"end":142835652,"strand":1,"description":"protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:9483]"}, {"versioned_ensembl_gene_id":"ENSG00000249988.1","gene_symbol":"AC092546.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14164455,"end":14242813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184560.7","gene_symbol":"C17orf74","gene_name":"chromosome 17 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201243","summary":null,"start":7425615,"end":7427568,"strand":1,"description":"chromosome 17 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27315]"}, {"versioned_ensembl_gene_id":"ENSG00000218728.3","gene_symbol":"KRT18P44","gene_name":"keratin 18 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:33414]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139748","summary":null,"start":128714506,"end":128715790,"strand":1,"description":"keratin 18 pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:33414]"}, {"versioned_ensembl_gene_id":"ENSG00000281191.2","gene_symbol":"KRTAP5-3","gene_name":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]","synonyms":"KRTAP5.3,KRTAP5-9","biotype":"protein_coding","ncbi_id":"387266","summary":null,"start":1607591,"end":1608489,"strand":-1,"description":"keratin associated protein 5-3 [Source:HGNC Symbol;Acc:HGNC:23598]"}, {"versioned_ensembl_gene_id":"ENSG00000280279.1","gene_symbol":"AC240565.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":64099,"end":76866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178287.17","gene_symbol":"SPAG11A","gene_name":"sperm associated antigen 11A [Source:HGNC Symbol;Acc:HGNC:33342]","synonyms":"HE2,EDDM2A","biotype":"protein_coding","ncbi_id":"653423","summary":null,"start":7847876,"end":7868867,"strand":1,"description":"sperm associated antigen 11A [Source:HGNC Symbol;Acc:HGNC:33342]"}, {"versioned_ensembl_gene_id":"ENSG00000248425.1","gene_symbol":"AC006296.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14390439,"end":14393992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272884.1","gene_symbol":"AC113189.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7439506,"end":7445966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262880.1","gene_symbol":"AC113189.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7420103,"end":7444081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226339.1","gene_symbol":"RPS26P56","gene_name":"ribosomal protein S26 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35858]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271400","summary":null,"start":129408382,"end":129408621,"strand":1,"description":"ribosomal protein S26 pseudogene 56 [Source:HGNC Symbol;Acc:HGNC:35858]"}, {"versioned_ensembl_gene_id":"ENSG00000262181.2","gene_symbol":"AP001005.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45034,"end":46047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127074.14","gene_symbol":"RGS13","gene_name":"regulator of G protein signaling 13 [Source:HGNC Symbol;Acc:HGNC:9995]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6003","summary":"The protein encoded by this gene is a member of the regulator of G protein signaling (RGS) family. RGS family members share similarity with S. cerevisiae SST2 and C. elegans egl-10 proteins, which contain a characteristic conserved RGS domain. RGS proteins accelerate GTPase activity of G protein alpha-subunits, thereby driving G protein into their inactive GDP-bound form, thus negatively regulating G protein signaling. RGS proteins have been implicated in the fine tuning of a variety of cellular events in response to G protein-coupled receptor activation. The biological function of this gene, however, is unknown. Two transcript variants encoding the same isoform exist. [provided by RefSeq, Jul 2008]","start":192636138,"end":192660306,"strand":1,"description":"regulator of G protein signaling 13 [Source:HGNC Symbol;Acc:HGNC:9995]"}, {"versioned_ensembl_gene_id":"ENSG00000257434.1","gene_symbol":"AC073525.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75020969,"end":75044793,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251412.1","gene_symbol":"AC006296.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":14383123,"end":14409078,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283647.1","gene_symbol":"AL512643.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":14790635,"end":14791158,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223995.2","gene_symbol":"RPL32P35","gene_name":"ribosomal protein L32 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36547]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271393","summary":null,"start":128838441,"end":128838834,"strand":-1,"description":"ribosomal protein L32 pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:36547]"}, {"versioned_ensembl_gene_id":"ENSG00000283439.1","gene_symbol":"AC113189.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7428903,"end":7432762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263301.1","gene_symbol":"AC113189.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7439159,"end":7443327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000072135.12","gene_symbol":"PTPN18","gene_name":"protein tyrosine phosphatase, non-receptor type 18 [Source:HGNC Symbol;Acc:HGNC:9649]","synonyms":"BDP1","biotype":"protein_coding","ncbi_id":"26469","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, the mitotic cycle, and oncogenic transformation. This PTP contains a PEST motif, which often serves as a protein-protein interaction domain, and may be related to protein intracellular half-live. This protein can differentially dephosphorylate autophosphorylated tyrosine kinases that are overexpressed in tumor tissues, and it appears to regulate HER2, a member of the epidermal growth factor receptor family of receptor tyrosine kinases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":130356007,"end":130375409,"strand":1,"description":"protein tyrosine phosphatase, non-receptor type 18 [Source:HGNC Symbol;Acc:HGNC:9649]"}, {"versioned_ensembl_gene_id":"ENSG00000243016.1","gene_symbol":"AC112482.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":127221194,"end":127221881,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204033.9","gene_symbol":"LRIT2","gene_name":"leucine rich repeat, Ig-like and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:23443]","synonyms":"LRRC22,AC022389.4","biotype":"protein_coding","ncbi_id":"340745","summary":null,"start":84220495,"end":84225589,"strand":-1,"description":"leucine rich repeat, Ig-like and transmembrane domains 2 [Source:HGNC Symbol;Acc:HGNC:23443]"}, {"versioned_ensembl_gene_id":"ENSG00000278620.3","gene_symbol":"KRTAP5-4","gene_name":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]","synonyms":"KRTAP5.4","biotype":"protein_coding","ncbi_id":"387267","summary":null,"start":1620988,"end":1622346,"strand":-1,"description":"keratin associated protein 5-4 [Source:HGNC Symbol;Acc:HGNC:23599]"}, {"versioned_ensembl_gene_id":"ENSG00000121211.7","gene_symbol":"MND1","gene_name":"meiotic nuclear divisions 1 [Source:HGNC Symbol;Acc:HGNC:24839]","synonyms":"GAJ","biotype":"protein_coding","ncbi_id":"84057","summary":"The product of the MND1 gene associates with HOP2 (MIM 608665) to form a stable heterodimeric complex that binds DNA and stimulates the recombinase activity of RAD51 (MIM 179617) and DMC1 (MIM 602721) (Chi et al., 2007 [PubMed 17639080]). Both the MND1 and HOP2 genes are indispensable for meiotic recombination.[supplied by OMIM, Mar 2008]","start":153344649,"end":153415118,"strand":1,"description":"meiotic nuclear divisions 1 [Source:HGNC Symbol;Acc:HGNC:24839]"}, {"versioned_ensembl_gene_id":"ENSG00000175065.11","gene_symbol":"DSG4","gene_name":"desmoglein 4 [Source:HGNC Symbol;Acc:HGNC:21307]","synonyms":"LAH,CDHF13","biotype":"protein_coding","ncbi_id":"147409","summary":"This gene encodes a member of the desmoglein subgroup of desmosomal cadherins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a transmembrane component of desmosomes and may play a role in cell-cell adhesion in epithelial cells. Mutations in the gene are associated with localized autosomal recessive hypotrichosis and monilethrix, characterized by impaired hair growth. [provided by RefSeq, May 2016]","start":31376777,"end":31414912,"strand":1,"description":"desmoglein 4 [Source:HGNC Symbol;Acc:HGNC:21307]"}, {"versioned_ensembl_gene_id":"ENSG00000262624.1","gene_symbol":"AC113189.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7436557,"end":7437523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000145451.12","gene_symbol":"GLRA3","gene_name":"glycine receptor alpha 3 [Source:HGNC Symbol;Acc:HGNC:4328]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8001","summary":"This gene encodes a member of the ligand-gated ion channel protein family. The encoded protein is a member of the glycine receptor subfamily. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]","start":174636914,"end":174829314,"strand":-1,"description":"glycine receptor alpha 3 [Source:HGNC Symbol;Acc:HGNC:4328]"}, {"versioned_ensembl_gene_id":"ENSG00000239620.1","gene_symbol":"AC133681.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":127284081,"end":127284681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181323.7","gene_symbol":"SPEM1","gene_name":"spermatid maturation 1 [Source:HGNC Symbol;Acc:HGNC:32429]","synonyms":"FLJ40081,C17orf83","biotype":"protein_coding","ncbi_id":"374768","summary":null,"start":7420360,"end":7421632,"strand":1,"description":"spermatid maturation 1 [Source:HGNC Symbol;Acc:HGNC:32429]"}, {"versioned_ensembl_gene_id":"ENSG00000176871.8","gene_symbol":"WSB2","gene_name":"WD repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:19222]","synonyms":"SBA2,MGC10210","biotype":"protein_coding","ncbi_id":"55884","summary":"This gene encodes a member of the WD-protein subfamily. The encoded protein contains five WD-repeats spanning most of the protein and an SOCS box in the C-terminus. The SOCS box may act as a bridge between specific substrate-binding domains and E3 ubiquitin protein ligases. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]","start":118032694,"end":118062430,"strand":-1,"description":"WD repeat and SOCS box containing 2 [Source:HGNC Symbol;Acc:HGNC:19222]"}, {"versioned_ensembl_gene_id":"ENSG00000188277.9","gene_symbol":"C15orf62","gene_name":"chromosome 15 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:34489]","synonyms":"LOC643338","biotype":"protein_coding","ncbi_id":"643338","summary":null,"start":40770080,"end":40772449,"strand":1,"description":"chromosome 15 open reading frame 62 [Source:HGNC Symbol;Acc:HGNC:34489]"}, {"versioned_ensembl_gene_id":"ENSG00000223614.5","gene_symbol":"ZNF735","gene_name":"zinc finger protein 735 [Source:HGNC Symbol;Acc:HGNC:32466]","synonyms":"ZNF735P","biotype":"protein_coding","ncbi_id":"730291","summary":"This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and nine C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017]","start":64207090,"end":64220508,"strand":1,"description":"zinc finger protein 735 [Source:HGNC Symbol;Acc:HGNC:32466]"}, {"versioned_ensembl_gene_id":"ENSG00000234592.1","gene_symbol":"AL359845.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":129041536,"end":129043183,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276432.4","gene_symbol":"RDM1","gene_name":"RAD52 motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19950]","synonyms":"RAD52B,MGC33977","biotype":"protein_coding","ncbi_id":"201299","summary":"This gene encodes a protein involved in the cellular response to cisplatin, a drug commonly used in chemotherapy. The protein encoded by this gene contains two motifs: a motif found in RAD52, a protein that functions in DNA double-strand breaks and homologous recombination, and an RNA recognition motif (RRM) that is not found in RAD52. The RAD52 motif region in RAD52 is important for protein function and may be involved in DNA binding or oligomerization. Alternatively spliced transcript variants encoding different isoforms have been reported. [provided by RefSeq, Jul 2008]","start":35918066,"end":35930773,"strand":-1,"description":"RAD52 motif containing 1 [Source:HGNC Symbol;Acc:HGNC:19950]"}, {"versioned_ensembl_gene_id":"ENSG00000231544.3","gene_symbol":"RSL24D1P11","gene_name":"ribosomal L24 domain containing 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37881]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"284288","summary":null,"start":57838476,"end":57838966,"strand":1,"description":"ribosomal L24 domain containing 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:37881]"}, {"versioned_ensembl_gene_id":"ENSG00000267209.5","gene_symbol":"LINC01897","gene_name":"long intergenic non-protein coding RNA 1897 [Source:HGNC Symbol;Acc:HGNC:52716]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985146","summary":null,"start":57961231,"end":57964434,"strand":-1,"description":"long intergenic non-protein coding RNA 1897 [Source:HGNC Symbol;Acc:HGNC:52716]"}, {"versioned_ensembl_gene_id":"ENSG00000251252.1","gene_symbol":"MTND2P31","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42132]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873235","summary":null,"start":14505865,"end":14506480,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 31 [Source:HGNC Symbol;Acc:HGNC:42132]"}, {"versioned_ensembl_gene_id":"ENSG00000248360.7","gene_symbol":"LINC00504","gene_name":"long intergenic non-protein coding RNA 504 [Source:HGNC Symbol;Acc:HGNC:43555]","synonyms":null,"biotype":"lincRNA","ncbi_id":"201853","summary":null,"start":14470465,"end":14888169,"strand":-1,"description":"long intergenic non-protein coding RNA 504 [Source:HGNC Symbol;Acc:HGNC:43555]"}, {"versioned_ensembl_gene_id":"ENSG00000266495.1","gene_symbol":"AC011731.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23257164,"end":23260354,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235028.3","gene_symbol":"HMGN1P30","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39374]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132992","summary":null,"start":58018794,"end":58019061,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:39374]"}, {"versioned_ensembl_gene_id":"ENSG00000161958.10","gene_symbol":"FGF11","gene_name":"fibroblast growth factor 11 [Source:HGNC Symbol;Acc:HGNC:3667]","synonyms":"MGC45269,MGC102953,FLJ16061,FHF3","biotype":"protein_coding","ncbi_id":"2256","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The function of this gene has not yet been determined. The expression pattern of the mouse homolog implies a role in nervous system development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":7438273,"end":7444937,"strand":1,"description":"fibroblast growth factor 11 [Source:HGNC Symbol;Acc:HGNC:3667]"}, {"versioned_ensembl_gene_id":"ENSG00000271286.1","gene_symbol":"U73023.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21939461,"end":21940160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276910.4","gene_symbol":"GTF2H2","gene_name":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]","synonyms":"TFIIH,T-BTF2P44,p44,BTF2P44,BTF2","biotype":"protein_coding","ncbi_id":"2966","summary":"This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq, Jul 2008]","start":70376388,"end":70411404,"strand":-1,"description":"general transcription factor IIH subunit 2 [Source:HGNC Symbol;Acc:HGNC:4656]"}, {"versioned_ensembl_gene_id":"ENSG00000281261.1","gene_symbol":"FAM99A","gene_name":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]","synonyms":"FLJ42833","biotype":"lincRNA","ncbi_id":"387742","summary":null,"start":1663142,"end":1665432,"strand":1,"description":"family with sequence similarity 99 member A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32368]"}, {"versioned_ensembl_gene_id":"ENSG00000228014.1","gene_symbol":"ZNF680P1","gene_name":"ZNF680 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50379]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728947","summary":null,"start":64469185,"end":64470653,"strand":1,"description":"ZNF680 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50379]"}, {"versioned_ensembl_gene_id":"ENSG00000227986.1","gene_symbol":"TRIM60P18","gene_name":"tripartite motif containing 60 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38490]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420415","summary":null,"start":64355078,"end":64356199,"strand":1,"description":"tripartite motif containing 60 pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:38490]"}, {"versioned_ensembl_gene_id":"ENSG00000269900.3","gene_symbol":"RMRP","gene_name":"RNA component of mitochondrial RNA processing endoribonuclease [Source:HGNC Symbol;Acc:HGNC:10031]","synonyms":"RRP2,RMRPR,RRP2,NME1,RMRPR,CHH,NME1,CHH","biotype":"lincRNA","ncbi_id":"6023","summary":"This gene encodes the RNA component of mitochondrial RNA processing endoribonuclease, which cleaves mitochondrial RNA at a priming site of mitochondrial DNA replication. This RNA also interacts with the telomerase reverse transcriptase catalytic subunit to form a distinct ribonucleoprotein complex that has RNA-dependent RNA polymerase activity and produces double-stranded RNAs that can be processed into small interfering RNA. Mutations in this gene are associated with cartilage-hair hypoplasia.[provided by RefSeq, Mar 2010]","start":35657751,"end":35658018,"strand":-1,"description":"RNA component of mitochondrial RNA processing endoribonuclease [Source:HGNC Symbol;Acc:HGNC:10031]"}, {"versioned_ensembl_gene_id":"ENSG00000232727.2","gene_symbol":"YWHAEP1","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49442]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649395","summary":null,"start":64433830,"end":64434592,"strand":1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49442]"}, {"versioned_ensembl_gene_id":"ENSG00000122591.11","gene_symbol":"FAM126A","gene_name":"family with sequence similarity 126 member A [Source:HGNC Symbol;Acc:HGNC:24587]","synonyms":"hyccin,HYCC1,HCC,DRCTNNB1A","biotype":"protein_coding","ncbi_id":"84668","summary":"The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008]","start":22889371,"end":23014130,"strand":-1,"description":"family with sequence similarity 126 member A [Source:HGNC Symbol;Acc:HGNC:24587]"}, {"versioned_ensembl_gene_id":"ENSG00000223845.1","gene_symbol":"VN1R40P","gene_name":"vomeronasal 1 receptor 40 pseudogene [Source:HGNC Symbol;Acc:HGNC:37360]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100312792","summary":null,"start":64443802,"end":64444742,"strand":-1,"description":"vomeronasal 1 receptor 40 pseudogene [Source:HGNC Symbol;Acc:HGNC:37360]"}, {"versioned_ensembl_gene_id":"ENSG00000276650.1","gene_symbol":"AC022202.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64425623,"end":64426334,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152291.13","gene_symbol":"TGOLN2","gene_name":"trans-golgi network protein 2 [Source:HGNC Symbol;Acc:HGNC:15450]","synonyms":"TTGN2,TGN51,TGN48,TGN46,TGN38","biotype":"protein_coding","ncbi_id":"10618","summary":"This gene encodes a type I integral membrane protein that is localized to the trans-Golgi network, a major sorting station for secretory and membrane proteins. The encoded protein cycles between early endosomes and the trans-Golgi network, and may play a role in exocytic vesicle formation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":85318020,"end":85328425,"strand":-1,"description":"trans-golgi network protein 2 [Source:HGNC Symbol;Acc:HGNC:15450]"}, {"versioned_ensembl_gene_id":"ENSG00000272476.1","gene_symbol":"AL024507.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107957413,"end":107959986,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224725.3","gene_symbol":"CEP57L1P1","gene_name":"centrosomal protein 57 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23521]","synonyms":"C6orf182P,C10orf37","biotype":"processed_pseudogene","ncbi_id":"221017","summary":null,"start":70389426,"end":70390626,"strand":1,"description":"centrosomal protein 57 like 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23521]"}, {"versioned_ensembl_gene_id":"ENSG00000268320.3","gene_symbol":"SCGB1C2","gene_name":"secretoglobin family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:51242]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653486","summary":null,"start":137526,"end":139067,"strand":1,"description":"secretoglobin family 1C member 2 [Source:HGNC Symbol;Acc:HGNC:51242]"}, {"versioned_ensembl_gene_id":"ENSG00000278430.4","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803354,"end":54814544,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000234444.9","gene_symbol":"ZNF736","gene_name":"zinc finger protein 736 [Source:HGNC Symbol;Acc:HGNC:32467]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728927","summary":null,"start":64307459,"end":64354860,"strand":1,"description":"zinc finger protein 736 [Source:HGNC Symbol;Acc:HGNC:32467]"}, {"versioned_ensembl_gene_id":"ENSG00000025796.13","gene_symbol":"SEC63","gene_name":"SEC63 homolog, protein translocation regulator [Source:HGNC Symbol;Acc:HGNC:21082]","synonyms":"SEC63L,PRO2507,ERdj2,DNAJC23","biotype":"protein_coding","ncbi_id":"11231","summary":"The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. The protein encoded by this gene and SEC62 protein are found to be associated with ribosome-free SEC61 complex. It is speculated that Sec61-Sec62-Sec63 may perform post-translational protein translocation into the ER. The Sec61-Sec62-Sec63 complex might also perform the backward transport of ER proteins that are subject to the ubiquitin-proteasome-dependent degradation pathway. The encoded protein is an integral membrane protein located in the rough ER. [provided by RefSeq, Jul 2008]","start":107867756,"end":107958189,"strand":-1,"description":"SEC63 homolog, protein translocation regulator [Source:HGNC Symbol;Acc:HGNC:21082]"}, {"versioned_ensembl_gene_id":"ENSG00000204104.11","gene_symbol":"TRAF3IP1","gene_name":"TRAF3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:17861]","synonyms":"MIP-T3,IFT54,DKFZP434F124,MIPT3","biotype":"protein_coding","ncbi_id":"26146","summary":"The protein encoded by this gene interacts with TNF receptor-associated factor 3, tethering it to cytoskeletal microtubules. The encoded protein is also an inhibitor of the innate type I IFN response. Defects in this gene are a cause of Senior-Loken syndrome 9. [provided by RefSeq, Mar 2017]","start":238320441,"end":238400900,"strand":1,"description":"TRAF3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:17861]"}, {"versioned_ensembl_gene_id":"ENSG00000214973.3","gene_symbol":"CHCHD3P3","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646572","summary":null,"start":27200834,"end":27201473,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44699]"}, {"versioned_ensembl_gene_id":"ENSG00000235727.7","gene_symbol":"HCG18","gene_name":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]","synonyms":"FLJ25550,Em:AB014087.1,FLJ31598","biotype":"processed_transcript","ncbi_id":"414777","summary":null,"start":30354705,"end":30391047,"strand":-1,"description":"HLA complex group 18 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31337]"}, {"versioned_ensembl_gene_id":"ENSG00000225159.1","gene_symbol":"NPM1P39","gene_name":"nucleophosmin 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:45218]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440577","summary":null,"start":27206930,"end":27207796,"strand":1,"description":"nucleophosmin 1 pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:45218]"}, {"versioned_ensembl_gene_id":"ENSG00000275779.4","gene_symbol":"NTAN1","gene_name":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]","synonyms":null,"biotype":"protein_coding","ncbi_id":"123803","summary":"The protein encoded by this gene functions in a step-wise process of protein degradation through the N-end rule pathway. This protein acts as a tertiary destabilizing enzyme that deamidates N-terminal L-Asn residues on proteins to produce N-terminal L-Asp. L-Asp substrates are subsequently conjugated to L-Arg, which is recognized by specific E3 ubiquitin ligases and targeted to the proteasome. Pseudogenes of this gene are located on the long arms of chromosomes 8, 10 and 12. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]","start":15040743,"end":15058977,"strand":1,"description":"N-terminal asparagine amidase [Source:HGNC Symbol;Acc:HGNC:29909]"}, {"versioned_ensembl_gene_id":"ENSG00000271914.1","gene_symbol":"AL139286.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35929720,"end":35930115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226467.9","gene_symbol":"AGPAT1","gene_name":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]","synonyms":"LPAAT-alpha","biotype":"protein_coding","ncbi_id":"10554","summary":"This gene encodes an enzyme that converts lysophosphatidic acid (LPA) into phosphatidic acid (PA). LPA and PA are two phospholipids involved in signal transduction and in lipid biosynthesis in cells. This enzyme localizes to the endoplasmic reticulum. This gene is located in the class III region of the human major histocompatibility complex. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]","start":32116683,"end":32126567,"strand":-1,"description":"1-acylglycerol-3-phosphate O-acyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:324]"}, {"versioned_ensembl_gene_id":"ENSG00000271164.1","gene_symbol":"AL139286.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35873270,"end":35873752,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225990.2","gene_symbol":"SNRPEP7","gene_name":"small nuclear ribonucleoprotein polypeptide E pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43572]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874415","summary":null,"start":27211265,"end":27211484,"strand":1,"description":"small nuclear ribonucleoprotein polypeptide E pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43572]"}, {"versioned_ensembl_gene_id":"ENSG00000224311.1","gene_symbol":"AL590640.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27229106,"end":27234352,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280136.2","gene_symbol":"AC240565.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":88641,"end":118578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184481.16","gene_symbol":"FOXO4","gene_name":"forkhead box O4 [Source:HGNC Symbol;Acc:HGNC:7139]","synonyms":"MLLT7,AFX1","biotype":"protein_coding","ncbi_id":"4303","summary":"This gene encodes a member of the O class of winged helix/forkhead transcription factor family. Proteins encoded by this class are regulated by factors involved in growth and differentiation indicating they play a role in these processes. A translocation involving this gene on chromosome X and the homolog of the Drosophila trithorax gene, encoding a DNA binding protein, located on chromosome 11 is associated with leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]","start":71096197,"end":71103535,"strand":1,"description":"forkhead box O4 [Source:HGNC Symbol;Acc:HGNC:7139]"}, {"versioned_ensembl_gene_id":"ENSG00000229690.1","gene_symbol":"MTCO2P1","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16564]","synonyms":"MTCO2L,dJ342K12.1","biotype":"processed_pseudogene","ncbi_id":"140909","summary":null,"start":60414396,"end":60414872,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16564]"}, {"versioned_ensembl_gene_id":"ENSG00000226710.9","gene_symbol":"C6orf48","gene_name":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]","synonyms":"D6S57,G8","biotype":"protein_coding","ncbi_id":"50854","summary":null,"start":31821974,"end":31827129,"strand":1,"description":"chromosome 6 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:19078]"}, {"versioned_ensembl_gene_id":"ENSG00000228340.5","gene_symbol":"MIR646HG","gene_name":"MIR646 host gene [Source:HGNC Symbol;Acc:HGNC:27659]","synonyms":null,"biotype":"lincRNA","ncbi_id":"284757","summary":null,"start":60087840,"end":60527458,"strand":1,"description":"MIR646 host gene [Source:HGNC Symbol;Acc:HGNC:27659]"}, {"versioned_ensembl_gene_id":"ENSG00000114374.12","gene_symbol":"USP9Y","gene_name":"ubiquitin specific peptidase 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:12633]","synonyms":"DFFRY","biotype":"protein_coding","ncbi_id":"8287","summary":"This gene is a member of the peptidase C19 family. It encodes a protein that is similar to ubiquitin-specific proteases, which cleave the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. [provided by RefSeq, Mar 2009]","start":12701231,"end":12860839,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:12633]"}, {"versioned_ensembl_gene_id":"ENSG00000278312.1","gene_symbol":"LENG9","gene_name":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]","synonyms":null,"biotype":"protein_coding","ncbi_id":"94059","summary":null,"start":54393938,"end":54395858,"strand":-1,"description":"leukocyte receptor cluster member 9 [Source:HGNC Symbol;Acc:HGNC:16306]"}, {"versioned_ensembl_gene_id":"ENSG00000157992.12","gene_symbol":"KRTCAP3","gene_name":"keratinocyte associated protein 3 [Source:HGNC Symbol;Acc:HGNC:28943]","synonyms":"KCP3","biotype":"protein_coding","ncbi_id":"200634","summary":null,"start":27442366,"end":27446481,"strand":1,"description":"keratinocyte associated protein 3 [Source:HGNC Symbol;Acc:HGNC:28943]"}, {"versioned_ensembl_gene_id":"ENSG00000276458.4","gene_symbol":"LENG8","gene_name":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]","synonyms":"pp13842,MGC40108,KIAA1932","biotype":"protein_coding","ncbi_id":"114823","summary":null,"start":54380864,"end":54394163,"strand":1,"description":"leukocyte receptor cluster member 8 [Source:HGNC Symbol;Acc:HGNC:15500]"}, {"versioned_ensembl_gene_id":"ENSG00000260865.1","gene_symbol":"AC010287.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":58597589,"end":58597945,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276259.1","gene_symbol":"AC009118.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58522970,"end":58523842,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224099.1","gene_symbol":"AC104823.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195448532,"end":195478925,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271893.1","gene_symbol":"AC064834.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":195451778,"end":195515699,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228590.1","gene_symbol":"AC007381.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60350595,"end":60353016,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000160200.17","gene_symbol":"CBS","gene_name":"cystathionine-beta-synthase [Source:HGNC Symbol;Acc:HGNC:1550]","synonyms":"HIP4","biotype":"protein_coding","ncbi_id":"875","summary":"The protein encoded by this gene acts as a homotetramer to catalyze the conversion of homocysteine to cystathionine, the first step in the transsulfuration pathway. The encoded protein is allosterically activated by adenosyl-methionine and uses pyridoxal phosphate as a cofactor. Defects in this gene can cause cystathionine beta-synthase deficiency (CBSD), which can lead to homocystinuria. This gene is a major contributor to cellular hydrogen sulfide production. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2016]","start":43053191,"end":43076943,"strand":-1,"description":"cystathionine-beta-synthase [Source:HGNC Symbol;Acc:HGNC:1550]"}, {"versioned_ensembl_gene_id":"ENSG00000261366.1","gene_symbol":"MANEA-AS1","gene_name":"MANEA antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43732]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927288","summary":null,"start":95575183,"end":95577450,"strand":-1,"description":"MANEA antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43732]"}, {"versioned_ensembl_gene_id":"ENSG00000280262.1","gene_symbol":"AC093671.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":140498402,"end":140501330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223466.1","gene_symbol":"LINC01825","gene_name":"long intergenic non-protein coding RNA 1825 [Source:HGNC Symbol;Acc:HGNC:52631]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985970","summary":null,"start":195533035,"end":195538681,"strand":1,"description":"long intergenic non-protein coding RNA 1825 [Source:HGNC Symbol;Acc:HGNC:52631]"}, {"versioned_ensembl_gene_id":"ENSG00000243832.1","gene_symbol":"LINC02000","gene_name":"long intergenic non-protein coding RNA 2000 [Source:HGNC Symbol;Acc:HGNC:52835]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507210","summary":null,"start":134055256,"end":134057648,"strand":-1,"description":"long intergenic non-protein coding RNA 2000 [Source:HGNC Symbol;Acc:HGNC:52835]"}, {"versioned_ensembl_gene_id":"ENSG00000223929.1","gene_symbol":"MIR4432HG","gene_name":"MIR4432 host gene [Source:HGNC Symbol;Acc:HGNC:52005]","synonyms":null,"biotype":"lincRNA","ncbi_id":"106660609","summary":null,"start":60359216,"end":60391375,"strand":-1,"description":"MIR4432 host gene [Source:HGNC Symbol;Acc:HGNC:52005]"}, {"versioned_ensembl_gene_id":"ENSG00000234919.1","gene_symbol":"LINC01827","gene_name":"long intergenic non-protein coding RNA 1827 [Source:HGNC Symbol;Acc:HGNC:52633]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373818","summary":null,"start":195569628,"end":195572970,"strand":-1,"description":"long intergenic non-protein coding RNA 1827 [Source:HGNC Symbol;Acc:HGNC:52633]"}, {"versioned_ensembl_gene_id":"ENSG00000172469.15","gene_symbol":"MANEA","gene_name":"mannosidase endo-alpha [Source:HGNC Symbol;Acc:HGNC:21072]","synonyms":"mandaselin,FLJ12838","biotype":"protein_coding","ncbi_id":"79694","summary":"N-glycosylation of proteins is initiated in the endoplasmic reticulum (ER) by the transfer of the preassembled oligosaccharide glucose-3-mannose-9-N-acetylglucosamine-2 from dolichyl pyrophosphate to acceptor sites on the target protein by an oligosaccharyltransferase complex. This core oligosaccharide is sequentially processed by several ER glycosidases and by an endomannosidase (E.C. 3.2.1.130), such as MANEA, in the Golgi. MANEA catalyzes the release of mono-, di-, and triglucosylmannose oligosaccharides by cleaving the alpha-1,2-mannosidic bond that links them to high-mannose glycans (Hamilton et al., 2005 [PubMed 15677381]).[supplied by OMIM, Sep 2008]","start":95577543,"end":95609457,"strand":1,"description":"mannosidase endo-alpha [Source:HGNC Symbol;Acc:HGNC:21072]"}, {"versioned_ensembl_gene_id":"ENSG00000134760.5","gene_symbol":"DSG1","gene_name":"desmoglein 1 [Source:HGNC Symbol;Acc:HGNC:3048]","synonyms":"DSG,CDHF4","biotype":"protein_coding","ncbi_id":"1828","summary":"This gene encodes a member of the desmoglein protein subfamily. Desmogleins, along with desmocollins, are cadherin-like transmembrane glycoproteins that are major components of the desmosome. Desmosomes are cell-cell junctions that help resist shearing forces and are found in high concentrations in cells subject to mechanical stress. This gene is found in a cluster with other desmoglein family members on chromosome 18. The encoded protein has been identified as a target of auto-antibodies in the autoimmune skin blistering disease pemphigus foliaceus. Disruption of this gene has also been associated with the skin diseases palmoplantar keratoderma and erythroderma. [provided by RefSeq, Feb 2015]","start":31318089,"end":31357029,"strand":1,"description":"desmoglein 1 [Source:HGNC Symbol;Acc:HGNC:3048]"}, {"versioned_ensembl_gene_id":"ENSG00000170180.20","gene_symbol":"GYPA","gene_name":"glycophorin A (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4702]","synonyms":"MNS,MN,GPA,CD235a","biotype":"protein_coding","ncbi_id":"2993","summary":"Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups. In addition to the M or N and S or s antigens that commonly occur in all populations, about 40 related variant phenotypes have been identified. These variants include all the variants of the Miltenberger complex and several isoforms of Sta, as well as Dantu, Sat, He, Mg, and deletion variants Ena, S-s-U- and Mk. Most of the variants are the result of gene recombinations between GYPA and GYPB. [provided by RefSeq, Jul 2008]","start":144109303,"end":144870953,"strand":-1,"description":"glycophorin A (MNS blood group) [Source:HGNC Symbol;Acc:HGNC:4702]"}, {"versioned_ensembl_gene_id":"ENSG00000157119.11","gene_symbol":"KLHL40","gene_name":"kelch like family member 40 [Source:HGNC Symbol;Acc:HGNC:30372]","synonyms":"SRYP,NEM8,KBTBD5","biotype":"protein_coding","ncbi_id":"131377","summary":"This gene encodes a protein containing a BACK domain, a BTB/POZ domain, and 5 Kelch repeats, however, its exact function is not known. The gene and the multi-domain protein structure are conserved across different taxa, including primates, rodents, chicken and zebrafish. [provided by RefSeq, Dec 2012]","start":42685519,"end":42692544,"strand":1,"description":"kelch like family member 40 [Source:HGNC Symbol;Acc:HGNC:30372]"}, {"versioned_ensembl_gene_id":"ENSG00000276292.1","gene_symbol":"AC131159.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118037869,"end":118038081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111445.13","gene_symbol":"RFC5","gene_name":"replication factor C subunit 5 [Source:HGNC Symbol;Acc:HGNC:9973]","synonyms":"RFC36","biotype":"protein_coding","ncbi_id":"5985","summary":"This gene encodes the smallest subunit of the replication factor C complex, which consists of five distinct subunits (140, 40, 38, 37, and 36 kDa) and is required for DNA replication. This subunit interacts with the C-terminal region of proliferating cell nuclear antigen and is required to open and load proliferating cell nuclear antigen onto DNA during S phase. It is a member of the AAA+ (ATPases associated with various cellular activities) ATPase family and forms a core complex with the 38 and 40 kDa subunits that possesses DNA-dependent ATPase activity. A related pseudogene has been identified on chromosome 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":118013588,"end":118033130,"strand":1,"description":"replication factor C subunit 5 [Source:HGNC Symbol;Acc:HGNC:9973]"}, {"versioned_ensembl_gene_id":"ENSG00000189180.15","gene_symbol":"ZNF33A","gene_name":"zinc finger protein 33A [Source:HGNC Symbol;Acc:HGNC:13096]","synonyms":"ZZAPK,ZNF33,ZNF11A,KOX5,KOX31,KIAA0065,FLJ23404","biotype":"protein_coding","ncbi_id":"7581","summary":null,"start":38010650,"end":38065088,"strand":1,"description":"zinc finger protein 33A [Source:HGNC Symbol;Acc:HGNC:13096]"}, {"versioned_ensembl_gene_id":"ENSG00000073737.16","gene_symbol":"DHRS9","gene_name":"dehydrogenase/reductase 9 [Source:HGNC Symbol;Acc:HGNC:16888]","synonyms":"RETSDR8,RDHL,RDH15,3alpha-HSD,SDR9C4","biotype":"protein_coding","ncbi_id":"10170","summary":"This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. This protein demonstrates oxidoreductase activity toward hydroxysteroids and is able to convert 3-alpha-tetrahydroprogesterone to dihydroxyprogesterone and 3-alpha-androstanediol to dihydroxyprogesterone in the cytoplasm, and may additionally function as a transcriptional repressor in the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":169064789,"end":169096167,"strand":1,"description":"dehydrogenase/reductase 9 [Source:HGNC Symbol;Acc:HGNC:16888]"}, {"versioned_ensembl_gene_id":"ENSG00000249550.6","gene_symbol":"LINC01234","gene_name":"long intergenic non-protein coding RNA 1234 [Source:HGNC Symbol;Acc:HGNC:49757]","synonyms":"onco-lncRNA-32","biotype":"lincRNA","ncbi_id":"100506465","summary":null,"start":113679459,"end":113773683,"strand":-1,"description":"long intergenic non-protein coding RNA 1234 [Source:HGNC Symbol;Acc:HGNC:49757]"}, {"versioned_ensembl_gene_id":"ENSG00000236729.6","gene_symbol":"HCG17","gene_name":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]","synonyms":"LINC00046,NCRNA00046","biotype":"processed_transcript","ncbi_id":"414778","summary":null,"start":30226495,"end":30390031,"strand":-1,"description":"HLA complex group 17 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:31339]"}, {"versioned_ensembl_gene_id":"ENSG00000232678.2","gene_symbol":"SPTLC1P4","gene_name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39671]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874500","summary":null,"start":152077952,"end":152078211,"strand":1,"description":"serine palmitoyltransferase long chain base subunit 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39671]"}, {"versioned_ensembl_gene_id":"ENSG00000260238.6","gene_symbol":"PMF1-BGLAP","gene_name":"PMF1-BGLAP readthrough [Source:HGNC Symbol;Acc:HGNC:42953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100527963","summary":"This locus represents naturally occurring read-through transcription between the neighboring PMF1 (polyamine-modulated factor 1) and BGLAP (bone gamma-carboxyglutamate Gla protein) genes on chromosome 1. Alternative splicing results in multiple transcript variants encoding isoforms that share sequence identity with the upstream gene product, but they contain distinct C-termini due to frameshifts versus the downstream gene coding sequence. [provided by RefSeq, Dec 2010]","start":156212982,"end":156243332,"strand":1,"description":"PMF1-BGLAP readthrough [Source:HGNC Symbol;Acc:HGNC:42953]"}, {"versioned_ensembl_gene_id":"ENSG00000168152.12","gene_symbol":"THAP9","gene_name":"THAP domain containing 9 [Source:HGNC Symbol;Acc:HGNC:23192]","synonyms":"FLJ34093","biotype":"protein_coding","ncbi_id":"79725","summary":null,"start":82900684,"end":82919969,"strand":1,"description":"THAP domain containing 9 [Source:HGNC Symbol;Acc:HGNC:23192]"}, {"versioned_ensembl_gene_id":"ENSG00000249434.1","gene_symbol":"TRIM26BP","gene_name":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]","synonyms":"Em:AB023053.1,TRIM26P1,TRIM26P","biotype":"unprocessed_pseudogene","ncbi_id":"404024","summary":null,"start":30230757,"end":30234733,"strand":1,"description":"tripartite motif containing 26B, pseudogene [Source:HGNC Symbol;Acc:HGNC:31338]"}, {"versioned_ensembl_gene_id":"ENSG00000213667.3","gene_symbol":"PGGT1BP1","gene_name":"protein geranylgeranyltransferase type I subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45024]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653895","summary":null,"start":50726947,"end":50727969,"strand":-1,"description":"protein geranylgeranyltransferase type I subunit beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45024]"}, {"versioned_ensembl_gene_id":"ENSG00000241779.6","gene_symbol":"RPP21","gene_name":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]","synonyms":"FLJ22638,Em:AB014085.3,C6orf135","biotype":"protein_coding","ncbi_id":"79897","summary":"RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]","start":30393209,"end":30410787,"strand":1,"description":"ribonuclease P/MRP subunit p21 [Source:HGNC Symbol;Acc:HGNC:21300]"}, {"versioned_ensembl_gene_id":"ENSG00000182898.3","gene_symbol":"TCHHL1","gene_name":"trichohyalin like 1 [Source:HGNC Symbol;Acc:HGNC:31796]","synonyms":"THHL1,S100A17","biotype":"protein_coding","ncbi_id":"126637","summary":"This gene belongs to the S100 fused-type protein (SFTP) gene family, and is located in a cluster of SFTP genes on chromosome 1q21. Several members of this family have been implicated in the development of complex skin disorders. This gene is evolutionarily conserved; its expression appears to be hair-specific and spatially restricted within the distal inner root sheath of the hair follicle. It thus may have an important role in hair morphogenesis. [provided by RefSeq, Aug 2013]","start":152084144,"end":152089064,"strand":-1,"description":"trichohyalin like 1 [Source:HGNC Symbol;Acc:HGNC:31796]"}, {"versioned_ensembl_gene_id":"ENSG00000089692.8","gene_symbol":"LAG3","gene_name":"lymphocyte activating 3 [Source:HGNC Symbol;Acc:HGNC:6476]","synonyms":"CD223","biotype":"protein_coding","ncbi_id":"3902","summary":"Lymphocyte-activation protein 3 belongs to Ig superfamily and contains 4 extracellular Ig-like domains. The LAG3 gene contains 8 exons. The sequence data, exon/intron organization, and chromosomal localization all indicate a close relationship of LAG3 to CD4. [provided by RefSeq, Jul 2008]","start":6772512,"end":6778455,"strand":1,"description":"lymphocyte activating 3 [Source:HGNC Symbol;Acc:HGNC:6476]"}, {"versioned_ensembl_gene_id":"ENSG00000257231.1","gene_symbol":"DYNLL1P4","gene_name":"dynein light chain LC8-type 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49655]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129739","summary":null,"start":113789542,"end":113789807,"strand":-1,"description":"dynein light chain LC8-type 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49655]"}, {"versioned_ensembl_gene_id":"ENSG00000266729.5","gene_symbol":"DSG1-AS1","gene_name":"DSG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51115]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927718","summary":null,"start":31343368,"end":31426988,"strand":-1,"description":"DSG1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51115]"}, {"versioned_ensembl_gene_id":"ENSG00000159450.12","gene_symbol":"TCHH","gene_name":"trichohyalin [Source:HGNC Symbol;Acc:HGNC:11791]","synonyms":"THH","biotype":"protein_coding","ncbi_id":"7062","summary":"The protein encoded by this gene forms crosslinked complexes with itself and keratin intermediate filaments to provide mechanical strength to the hair follicle inner root sheath. The encoded protein also is important for structural integrity of the filiform papillae of the tongue. Defects in this gene are a cause of uncombable hair syndrome. [provided by RefSeq, Feb 2017]","start":152106317,"end":152115454,"strand":-1,"description":"trichohyalin [Source:HGNC Symbol;Acc:HGNC:11791]"}, {"versioned_ensembl_gene_id":"ENSG00000225544.1","gene_symbol":"AC245452.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21885282,"end":21885673,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142784.15","gene_symbol":"WDTC1","gene_name":"WD and tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:29175]","synonyms":"KIAA1037,DCAF9,ADP","biotype":"protein_coding","ncbi_id":"23038","summary":null,"start":27234516,"end":27308633,"strand":1,"description":"WD and tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:HGNC:29175]"}, {"versioned_ensembl_gene_id":"ENSG00000214047.4","gene_symbol":"RPS11P7","gene_name":"ribosomal protein S11 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642687","summary":null,"start":39865424,"end":39865888,"strand":1,"description":"ribosomal protein S11 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:36724]"}, {"versioned_ensembl_gene_id":"ENSG00000213987.4","gene_symbol":"AC093151.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41264550,"end":41264862,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143183.16","gene_symbol":"TMCO1","gene_name":"transmembrane and coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:18188]","synonyms":"HP10122,TMCC4","biotype":"protein_coding","ncbi_id":"54499","summary":"This locus encodes a transmembrane protein. Mutations at this locus have been associated with craniofacial dysmorphism, skeletal anomalies, and cognitive disability. Mutations at this locus have also been associated with open angle glaucoma blindness. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]","start":165724293,"end":165827755,"strand":-1,"description":"transmembrane and coiled-coil domains 1 [Source:HGNC Symbol;Acc:HGNC:18188]"}, {"versioned_ensembl_gene_id":"ENSG00000235358.1","gene_symbol":"AC093151.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41242373,"end":41284861,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235267.1","gene_symbol":"AC074117.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27455156,"end":27455862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277389.1","gene_symbol":"KRTAP5-6","gene_name":"keratin associated protein 5-6 [Source:HGNC Symbol;Acc:HGNC:23600]","synonyms":"KRTAP5.6","biotype":"protein_coding","ncbi_id":"440023","summary":null,"start":1694414,"end":1694974,"strand":1,"description":"keratin associated protein 5-6 [Source:HGNC Symbol;Acc:HGNC:23600]"}, {"versioned_ensembl_gene_id":"ENSG00000148730.6","gene_symbol":"EIF4EBP2","gene_name":"eukaryotic translation initiation factor 4E binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3289]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1979","summary":"This gene encodes a member of the eukaryotic translation initiation factor 4E binding protein family. The gene products of this family bind eIF4E and inhibit translation initiation. However, insulin and other growth factors can release this inhibition via a phosphorylation-dependent disruption of their binding to eIF4E. Regulation of protein production through these gene products have been implicated in cell proliferation, cell differentiation and viral infection. [provided by RefSeq, Oct 2008]","start":70404379,"end":70428618,"strand":1,"description":"eukaryotic translation initiation factor 4E binding protein 2 [Source:HGNC Symbol;Acc:HGNC:3289]"}, {"versioned_ensembl_gene_id":"ENSG00000274957.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i","biotype":"protein_coding","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832707,"end":54848622,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000142657.20","gene_symbol":"PGD","gene_name":"phosphogluconate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8891]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5226","summary":"6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]","start":10398592,"end":10420144,"strand":1,"description":"phosphogluconate dehydrogenase [Source:HGNC Symbol;Acc:HGNC:8891]"}, {"versioned_ensembl_gene_id":"ENSG00000282717.1","gene_symbol":"AC243651.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15080438,"end":15081000,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138002.14","gene_symbol":"IFT172","gene_name":"intraflagellar transport 172 [Source:HGNC Symbol;Acc:HGNC:30391]","synonyms":"BBS20,wim,SLB,osm-1,NPHP17","biotype":"protein_coding","ncbi_id":"26160","summary":"This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]","start":27444371,"end":27489789,"strand":-1,"description":"intraflagellar transport 172 [Source:HGNC Symbol;Acc:HGNC:30391]"}, {"versioned_ensembl_gene_id":"ENSG00000278440.1","gene_symbol":"AC243791.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15106659,"end":15108560,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281829.1","gene_symbol":"FAM99B","gene_name":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]","synonyms":"DKFZp781M09150","biotype":"antisense_RNA","ncbi_id":"100132464","summary":null,"start":1680530,"end":1682598,"strand":-1,"description":"family with sequence similarity 99 member B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:32369]"}, {"versioned_ensembl_gene_id":"ENSG00000275593.4","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786351,"end":54798281,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000281633.1","gene_symbol":"AC130310.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1685548,"end":1686307,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277067.4","gene_symbol":"CU634019.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7048891,"end":7087229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278821.4","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769815,"end":54784318,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000251022.6","gene_symbol":"THAP9-AS1","gene_name":"THAP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44172]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100499177","summary":null,"start":82893009,"end":82900960,"strand":-1,"description":"THAP9 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44172]"}, {"versioned_ensembl_gene_id":"ENSG00000122512.14","gene_symbol":"PMS2","gene_name":"PMS1 homolog 2, mismatch repair system component [Source:HGNC Symbol;Acc:HGNC:9122]","synonyms":"MLH4,H_DJ0042M02.9,HNPCC4,PMSL2","biotype":"protein_coding","ncbi_id":"5395","summary":"The protein encoded by this gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and homologous recombination. This protein forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer. The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers, and is necessary for removal of the mismatched DNA. There is a DQHA(X)2E(X)4E motif found at the C-terminus of the protein encoded by this gene that forms part of the active site of the nuclease. Mutations in this gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC; also known as Lynch syndrome) and Turcot syndrome. [provided by RefSeq, Apr 2016]","start":5973239,"end":6009125,"strand":-1,"description":"PMS1 homolog 2, mismatch repair system component [Source:HGNC Symbol;Acc:HGNC:9122]"}, {"versioned_ensembl_gene_id":"ENSG00000104290.10","gene_symbol":"FZD3","gene_name":"frizzled class receptor 3 [Source:HGNC Symbol;Acc:HGNC:4041]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7976","summary":"This gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. The function of this protein is unknown, although it may play a role in mammalian hair follicle development. Alternative splicing results in multiple transcript variants. This gene is a susceptibility locus for schizophrenia. [provided by RefSeq, Dec 2010]","start":28494205,"end":28574268,"strand":1,"description":"frizzled class receptor 3 [Source:HGNC Symbol;Acc:HGNC:4041]"}, {"versioned_ensembl_gene_id":"ENSG00000280401.1","gene_symbol":"AC022532.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70434829,"end":70436556,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000156574.9","gene_symbol":"NODAL","gene_name":"nodal growth differentiation factor [Source:HGNC Symbol;Acc:HGNC:7865]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4838","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which regulates early embryonic development. This protein is required for maintenance of human embryonic stem cell pluripotency and may play a role in human placental development. Mutations in this gene are associated with heterotaxy, a condition characterized by random orientation of visceral organs with respect to the left-right axis. [provided by RefSeq, Aug 2016]","start":70432315,"end":70447951,"strand":-1,"description":"nodal growth differentiation factor [Source:HGNC Symbol;Acc:HGNC:7865]"}, {"versioned_ensembl_gene_id":"ENSG00000243659.1","gene_symbol":"FO393419.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27311240,"end":27311838,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234565.1","gene_symbol":"COX6B1P1","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2281]","synonyms":"COX6BP1","biotype":"processed_pseudogene","ncbi_id":"140603","summary":null,"start":149053961,"end":149054173,"strand":1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2281]"}, {"versioned_ensembl_gene_id":"ENSG00000160783.19","gene_symbol":"PMF1","gene_name":"polyamine modulated factor 1 [Source:HGNC Symbol;Acc:HGNC:9112]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11243","summary":null,"start":156212993,"end":156240042,"strand":1,"description":"polyamine modulated factor 1 [Source:HGNC Symbol;Acc:HGNC:9112]"}, {"versioned_ensembl_gene_id":"ENSG00000228411.1","gene_symbol":"CDY4P","gene_name":"chromodomain Y-linked 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:23872]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"386729","summary":null,"start":12801973,"end":12803830,"strand":-1,"description":"chromodomain Y-linked 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:23872]"}, {"versioned_ensembl_gene_id":"ENSG00000204165.5","gene_symbol":"CXorf65","gene_name":"chromosome X open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:33713]","synonyms":null,"biotype":"protein_coding","ncbi_id":"158830","summary":null,"start":71103889,"end":71106788,"strand":-1,"description":"chromosome X open reading frame 65 [Source:HGNC Symbol;Acc:HGNC:33713]"}, {"versioned_ensembl_gene_id":"ENSG00000236427.1","gene_symbol":"AL589986.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":152205858,"end":152207057,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282484.1","gene_symbol":"AC022257.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2199057,"end":2201817,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277219.1","gene_symbol":"AC146335.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70249980,"end":70275822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231304.2","gene_symbol":"SGO1-AS1","gene_name":"SGO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41081]","synonyms":"SGOL1-AS1","biotype":"processed_transcript","ncbi_id":"100874028","summary":null,"start":20174244,"end":21145967,"strand":1,"description":"SGO1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41081]"}, {"versioned_ensembl_gene_id":"ENSG00000143536.7","gene_symbol":"CRNN","gene_name":"cornulin [Source:HGNC Symbol;Acc:HGNC:1230]","synonyms":"SEP53,C1orf10","biotype":"protein_coding","ncbi_id":"49860","summary":"This gene encodes a member of the \"fused gene\" family of proteins, which contain N-terminus EF-hand domains and multiple tandem peptide repeats. The encoded protein contains two EF-hand Ca2+ binding domains in its N-terminus and two glutamine- and threonine-rich 60 amino acid repeats in its C-terminus. This gene, also known as squamous epithelial heat shock protein 53, may play a role in the mucosal/epithelial immune response and epidermal differentiation. [provided by RefSeq, Jan 2009]","start":152409243,"end":152414263,"strand":-1,"description":"cornulin [Source:HGNC Symbol;Acc:HGNC:1230]"}, {"versioned_ensembl_gene_id":"ENSG00000224452.1","gene_symbol":"RSL24D1P6","gene_name":"ribosomal L24 domain containing 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37876]","synonyms":"RPL24P1,dJ836N17.3","biotype":"processed_pseudogene","ncbi_id":"140757","summary":null,"start":32170390,"end":32170790,"strand":-1,"description":"ribosomal L24 domain containing 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37876]"}, {"versioned_ensembl_gene_id":"ENSG00000282492.1","gene_symbol":"WBP1LP1","gene_name":"WW domain binding protein 1-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43948]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479029","summary":null,"start":142839736,"end":142840629,"strand":-1,"description":"WW domain binding protein 1-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43948]"}, {"versioned_ensembl_gene_id":"ENSG00000273935.1","gene_symbol":"CDH12P4","gene_name":"cadherin 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37700]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100093626","summary":null,"start":70280062,"end":70280356,"strand":1,"description":"cadherin 12 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37700]"}, {"versioned_ensembl_gene_id":"ENSG00000232778.1","gene_symbol":"RPL23AP50","gene_name":"ribosomal protein L23a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35958]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728106","summary":null,"start":107931800,"end":107932254,"strand":1,"description":"ribosomal protein L23a pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:35958]"}, {"versioned_ensembl_gene_id":"ENSG00000282253.1","gene_symbol":"AC239618.6","gene_name":null,"synonyms":null,"biotype":"TR_D_gene","ncbi_id":null,"summary":null,"start":142847306,"end":142847317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197362.14","gene_symbol":"ZNF786","gene_name":"zinc finger protein 786 [Source:HGNC Symbol;Acc:HGNC:21806]","synonyms":"DKFZp762I137","biotype":"protein_coding","ncbi_id":"136051","summary":null,"start":149069643,"end":149090782,"strand":-1,"description":"zinc finger protein 786 [Source:HGNC Symbol;Acc:HGNC:21806]"}, {"versioned_ensembl_gene_id":"ENSG00000282078.1","gene_symbol":"AC239618.4","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142847973,"end":142848020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137251.15","gene_symbol":"TINAG","gene_name":"tubulointerstitial nephritis antigen [Source:HGNC Symbol;Acc:HGNC:14599]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27283","summary":"This gene encodes a glycoprotein that is restricted within the kidney to the basement membranes underlying the epithelium of Bowman's capsule and proximal and distal tubules. Autoantibodies against this protein are found in sera of patients with tubulointerstital nephritis, membranous nephropathy and anti-glomerular basement membrane nephritis. Ontogeny studies suggest that the expression of this antigen is developmentally regulated in a precise spatial and temporal pattern throughout nephrogenesis. [provided by RefSeq, Nov 2011]","start":54307859,"end":54390152,"strand":1,"description":"tubulointerstitial nephritis antigen [Source:HGNC Symbol;Acc:HGNC:14599]"}, {"versioned_ensembl_gene_id":"ENSG00000183629.13","gene_symbol":"GOLGA8G","gene_name":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]","synonyms":"DKFZp434K052","biotype":"protein_coding","ncbi_id":"283768","summary":null,"start":28519611,"end":28533014,"strand":-1,"description":"golgin A8 family member G [Source:HGNC Symbol;Acc:HGNC:25328]"}, {"versioned_ensembl_gene_id":"ENSG00000273799.1","gene_symbol":"AC146335.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":70344694,"end":70355160,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215853.3","gene_symbol":"RPTN","gene_name":"repetin [Source:HGNC Symbol;Acc:HGNC:26809]","synonyms":"FLJ39117","biotype":"protein_coding","ncbi_id":"126638","summary":null,"start":152153595,"end":152159228,"strand":-1,"description":"repetin [Source:HGNC Symbol;Acc:HGNC:26809]"}, {"versioned_ensembl_gene_id":"ENSG00000130303.12","gene_symbol":"BST2","gene_name":"bone marrow stromal cell antigen 2 [Source:HGNC Symbol;Acc:HGNC:1119]","synonyms":"tetherin,CD317","biotype":"protein_coding","ncbi_id":"684","summary":"Bone marrow stromal cells are involved in the growth and development of B-cells. The specific function of the protein encoded by the bone marrow stromal cell antigen 2 is undetermined; however, this protein may play a role in pre-B-cell growth and in rheumatoid arthritis. [provided by RefSeq, Jul 2008]","start":17402939,"end":17405648,"strand":-1,"description":"bone marrow stromal cell antigen 2 [Source:HGNC Symbol;Acc:HGNC:1119]"}, {"versioned_ensembl_gene_id":"ENSG00000231767.3","gene_symbol":"AL136454.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":192716183,"end":192716648,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143520.6","gene_symbol":"FLG2","gene_name":"filaggrin family member 2 [Source:HGNC Symbol;Acc:HGNC:33276]","synonyms":"IFPS","biotype":"protein_coding","ncbi_id":"388698","summary":"The filaggrin-like protein encoded by this gene is upregulated by calcium, proteolyzed by calpain 1, and is involved in epithelial homeostasis. The encoded protein is required for proper cornification in skin, with defects in this gene being associated with skin diseases. This protein also has a function in skin barrier protection. In fact, in addition to providing a physical barrier, C-terminal fragments of this protein display antimicrobial activity against P. aeruginosa and E. coli. [provided by RefSeq, Jul 2020]","start":152348735,"end":152360006,"strand":-1,"description":"filaggrin family member 2 [Source:HGNC Symbol;Acc:HGNC:33276]"}, {"versioned_ensembl_gene_id":"ENSG00000168135.4","gene_symbol":"KCNJ4","gene_name":"potassium voltage-gated channel subfamily J member 4 [Source:HGNC Symbol;Acc:HGNC:6265]","synonyms":"Kir2.3,IRK3,HRK1,hIRK2,HIR","biotype":"protein_coding","ncbi_id":"3761","summary":"Several different potassium channels are known to be involved with electrical signaling in the nervous system. One class is activated by depolarization whereas a second class is not. The latter are referred to as inwardly rectifying K+ channels, and they have a greater tendency to allow potassium to flow into the cell rather than out of it. This asymmetry in potassium ion conductance plays a key role in the excitability of muscle cells and neurons. The protein encoded by this gene is an integral membrane protein and member of the inward rectifier potassium channel family. The encoded protein has a small unitary conductance compared to other members of this protein family. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":38426327,"end":38455199,"strand":-1,"description":"potassium voltage-gated channel subfamily J member 4 [Source:HGNC Symbol;Acc:HGNC:6265]"}, {"versioned_ensembl_gene_id":"ENSG00000151360.9","gene_symbol":"ALLC","gene_name":"allantoicase [Source:HGNC Symbol;Acc:HGNC:17377]","synonyms":"ALC","biotype":"protein_coding","ncbi_id":"55821","summary":"Allantoicase (EC 3.5.3.4) participates in the uric acid degradation pathway. Its enzymatic activity, like that of urate oxidase (MIM 191540), was lost during vertebrate evolution.[supplied by OMIM, Nov 2008]","start":3658195,"end":3702671,"strand":1,"description":"allantoicase [Source:HGNC Symbol;Acc:HGNC:17377]"}, {"versioned_ensembl_gene_id":"ENSG00000197915.5","gene_symbol":"HRNR","gene_name":"hornerin [Source:HGNC Symbol;Acc:HGNC:20846]","synonyms":"S100a18,S100A16,FLG3","biotype":"protein_coding","ncbi_id":"388697","summary":null,"start":152212082,"end":152224193,"strand":-1,"description":"hornerin [Source:HGNC Symbol;Acc:HGNC:20846]"}, {"versioned_ensembl_gene_id":"ENSG00000228620.1","gene_symbol":"Z97056.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38424288,"end":38427336,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278614.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755019,"end":54767464,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000236519.1","gene_symbol":"LINC01424","gene_name":"long intergenic non-protein coding RNA 1424 [Source:HGNC Symbol;Acc:HGNC:40558]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928689","summary":null,"start":44802577,"end":44804717,"strand":1,"description":"long intergenic non-protein coding RNA 1424 [Source:HGNC Symbol;Acc:HGNC:40558]"}, {"versioned_ensembl_gene_id":"ENSG00000282263.1","gene_symbol":"AC133633.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2478186,"end":2496887,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226471.6","gene_symbol":"Z93930.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28800683,"end":28848559,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277175.5","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816466,"end":54830808,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000183586.8","gene_symbol":"HMGN3P1","gene_name":"high mobility group nucleosomal binding domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39206]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100289191","summary":null,"start":152399577,"end":152399769,"strand":1,"description":"high mobility group nucleosomal binding domain 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39206]"}, {"versioned_ensembl_gene_id":"ENSG00000226716.1","gene_symbol":"AL589986.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":152122534,"end":152125065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143631.10","gene_symbol":"FLG","gene_name":"filaggrin [Source:HGNC Symbol;Acc:HGNC:3748]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2312","summary":"The protein encoded by this gene is an intermediate filament-associated protein that aggregates keratin intermediate filaments in mammalian epidermis. It is initially synthesized as a polyprotein precursor, profilaggrin (consisting of multiple filaggrin units of 324 aa each), which is localized in keratohyalin granules, and is subsequently proteolytically processed into individual functional filaggrin molecules. Mutations in this gene are associated with ichthyosis vulgaris.[provided by RefSeq, Dec 2009]","start":152302175,"end":152325203,"strand":-1,"description":"filaggrin [Source:HGNC Symbol;Acc:HGNC:3748]"}, {"versioned_ensembl_gene_id":"ENSG00000269720.2","gene_symbol":"CCDC194","gene_name":"coiled-coil domain containing 194 [Source:HGNC Symbol;Acc:HGNC:53438]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":17390509,"end":17394158,"strand":-1,"description":"coiled-coil domain containing 194 [Source:HGNC Symbol;Acc:HGNC:53438]"}, {"versioned_ensembl_gene_id":"ENSG00000224256.1","gene_symbol":"Z93930.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28835893,"end":28836137,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272858.1","gene_symbol":"Z93930.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28814914,"end":28815662,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282987.1","gene_symbol":"AC099753.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21006730,"end":21226305,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230256.1","gene_symbol":"FGFR1OP2P1","gene_name":"FGFR1 oncogene partner 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39706]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873883","summary":null,"start":26905362,"end":26905861,"strand":1,"description":"FGFR1 oncogene partner 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39706]"}, {"versioned_ensembl_gene_id":"ENSG00000272050.1","gene_symbol":"AL499627.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62477870,"end":62478594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172939.8","gene_symbol":"OXSR1","gene_name":"oxidative stress responsive 1 [Source:HGNC Symbol;Acc:HGNC:8508]","synonyms":"OSR1,KIAA1101","biotype":"protein_coding","ncbi_id":"9943","summary":"The product of this gene belongs to the Ser/Thr protein kinase family of proteins. It regulates downstream kinases in response to environmental stress, and may play a role in regulating the actin cytoskeleton. [provided by RefSeq, Jul 2008]","start":38165089,"end":38255488,"strand":1,"description":"oxidative stress responsive 1 [Source:HGNC Symbol;Acc:HGNC:8508]"}, {"versioned_ensembl_gene_id":"ENSG00000125851.9","gene_symbol":"PCSK2","gene_name":"proprotein convertase subtilisin/kexin type 2 [Source:HGNC Symbol;Acc:HGNC:8744]","synonyms":"SPC2,PC2,NEC2","biotype":"protein_coding","ncbi_id":"5126","summary":"This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The protein undergoes an initial autocatalytic processing event and interacts with a neuroendocrine secretory protein in the ER, exits the ER and sorts to secretory granules, where it is cleaved and catalytically activated during intracellular transport. The encoded protease is packaged into and activated in dense core secretory granules and expressed in the neuroendocrine system and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It functions in the proteolytic activation of polypeptide hormones and neuropeptides precursors. Single nucleotide polymorphisms in this gene may increase susceptibility to myocardial infarction and type 2 diabetes. This gene may also play a role in tumor development and progression. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2014]","start":17226107,"end":17484578,"strand":1,"description":"proprotein convertase subtilisin/kexin type 2 [Source:HGNC Symbol;Acc:HGNC:8744]"}, {"versioned_ensembl_gene_id":"ENSG00000261734.1","gene_symbol":"AC116096.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20388249,"end":20390562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281122.1","gene_symbol":"AC108866.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":120165490,"end":120165892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137135.17","gene_symbol":"ARHGEF39","gene_name":"Rho guanine nucleotide exchange factor 39 [Source:HGNC Symbol;Acc:HGNC:25909]","synonyms":"FLJ14642,C9orf100","biotype":"protein_coding","ncbi_id":"84904","summary":null,"start":35658875,"end":35675866,"strand":-1,"description":"Rho guanine nucleotide exchange factor 39 [Source:HGNC Symbol;Acc:HGNC:25909]"}, {"versioned_ensembl_gene_id":"ENSG00000223486.1","gene_symbol":"AC092198.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40009276,"end":40012182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281482.1","gene_symbol":"AC093789.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":188349376,"end":188350024,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000087586.17","gene_symbol":"AURKA","gene_name":"aurora kinase A [Source:HGNC Symbol;Acc:HGNC:11393]","synonyms":"BTAK,AurA,ARK1,AIK,STK7,STK6,STK15,PPP1R47","biotype":"protein_coding","ncbi_id":"6790","summary":"The protein encoded by this gene is a cell cycle-regulated kinase that appears to be involved in microtubule formation and/or stabilization at the spindle pole during chromosome segregation. The encoded protein is found at the centrosome in interphase cells and at the spindle poles in mitosis. This gene may play a role in tumor development and progression. A processed pseudogene of this gene has been found on chromosome 1, and an unprocessed pseudogene has been found on chromosome 10. Multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":56369389,"end":56392337,"strand":-1,"description":"aurora kinase A [Source:HGNC Symbol;Acc:HGNC:11393]"}, {"versioned_ensembl_gene_id":"ENSG00000233792.3","gene_symbol":"PUDPP2","gene_name":"pseudouridine 5'-phosphatase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20195]","synonyms":"HDHD1P2,HDHD1CP,FAM16B","biotype":"transcribed_processed_pseudogene","ncbi_id":"327659","summary":null,"start":152124016,"end":152196699,"strand":-1,"description":"pseudouridine 5'-phosphatase pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:20195]"}, {"versioned_ensembl_gene_id":"ENSG00000224661.1","gene_symbol":"AC010907.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3702585,"end":3704153,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281800.1","gene_symbol":"ICE2P1","gene_name":"interactor of little elongation complex ELL subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48856]","synonyms":"NARG2P1","biotype":"processed_pseudogene","ncbi_id":"644491","summary":null,"start":188387471,"end":188389666,"strand":-1,"description":"interactor of little elongation complex ELL subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48856]"}, {"versioned_ensembl_gene_id":"ENSG00000214866.8","gene_symbol":"DCDC2C","gene_name":"doublecortin domain containing 2C [Source:HGNC Symbol;Acc:HGNC:32696]","synonyms":null,"biotype":"protein_coding","ncbi_id":"728597","summary":null,"start":3703592,"end":3847411,"strand":1,"description":"doublecortin domain containing 2C [Source:HGNC Symbol;Acc:HGNC:32696]"}, {"versioned_ensembl_gene_id":"ENSG00000256073.3","gene_symbol":"URB1-AS1","gene_name":"URB1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:23128]","synonyms":"PRED84,MGC14136,C21orf119","biotype":"lincRNA","ncbi_id":"84996","summary":null,"start":32393130,"end":32393960,"strand":1,"description":"URB1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:23128]"}, {"versioned_ensembl_gene_id":"ENSG00000242252.1","gene_symbol":"BGLAP","gene_name":"bone gamma-carboxyglutamate protein [Source:HGNC Symbol;Acc:HGNC:1043]","synonyms":"OCN","biotype":"protein_coding","ncbi_id":"632","summary":"This gene encodes a highly abundant bone protein secreted by osteoblasts that regulates bone remodeling and energy metabolism. The encoded protein contains a Gla (gamma carboxyglutamate) domain, which functions in binding to calcium and hydroxyapatite, the mineral component of bone. Serum osteocalcin levels may be negatively correlated with metabolic syndrome. Read-through transcription exists between this gene and the neighboring upstream gene, PMF1 (polyamine-modulated factor 1), but the encoded protein only shows sequence identity with the upstream gene product. [provided by RefSeq, Jun 2015]","start":156241962,"end":156243321,"strand":1,"description":"bone gamma-carboxyglutamate protein [Source:HGNC Symbol;Acc:HGNC:1043]"}, {"versioned_ensembl_gene_id":"ENSG00000132975.7","gene_symbol":"GPR12","gene_name":"G protein-coupled receptor 12 [Source:HGNC Symbol;Acc:HGNC:4466]","synonyms":"PPP1R84,GPCR21","biotype":"protein_coding","ncbi_id":"2835","summary":null,"start":26755200,"end":26760785,"strand":-1,"description":"G protein-coupled receptor 12 [Source:HGNC Symbol;Acc:HGNC:4466]"}, {"versioned_ensembl_gene_id":"ENSG00000224573.1","gene_symbol":"AC083863.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32951426,"end":32951656,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277873.1","gene_symbol":"AC131159.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118024817,"end":118025518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100201.20","gene_symbol":"DDX17","gene_name":"DEAD-box helicase 17 [Source:HGNC Symbol;Acc:HGNC:2740]","synonyms":"P72","biotype":"protein_coding","ncbi_id":"10521","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and splicesosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an ATPase activated by a variety of RNA species, but not by dsDNA. This protein, and that encoded by DDX5 gene, are more closely related to each other than to any other member of the DEAD box family. This gene can encode multiple isoforms due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) start codon. [provided by RefSeq, Apr 2011]","start":38483440,"end":38507660,"strand":-1,"description":"DEAD-box helicase 17 [Source:HGNC Symbol;Acc:HGNC:2740]"}, {"versioned_ensembl_gene_id":"ENSG00000230547.1","gene_symbol":"HMGB1P11","gene_name":"high mobility group box 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:13316]","synonyms":"HMGB1L11","biotype":"processed_pseudogene","ncbi_id":"100419996","summary":null,"start":171270954,"end":171271590,"strand":-1,"description":"high mobility group box 1 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:13316]"}, {"versioned_ensembl_gene_id":"ENSG00000271141.1","gene_symbol":"AC010680.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":178616581,"end":178617123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000010932.16","gene_symbol":"FMO1","gene_name":"flavin containing monooxygenase 1 [Source:HGNC Symbol;Acc:HGNC:3769]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2326","summary":"Metabolic N-oxidation of the diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man resulting in a small subpopulation with reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found in adult liver, and FMO3 are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":171248471,"end":171285978,"strand":1,"description":"flavin containing monooxygenase 1 [Source:HGNC Symbol;Acc:HGNC:3769]"}, {"versioned_ensembl_gene_id":"ENSG00000260542.1","gene_symbol":"AL499627.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62513909,"end":62516096,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230649.2","gene_symbol":"AC024084.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136025761,"end":136084668,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163492.14","gene_symbol":"CCDC141","gene_name":"coiled-coil domain containing 141 [Source:HGNC Symbol;Acc:HGNC:26821]","synonyms":"FLJ39502,CAMDI","biotype":"protein_coding","ncbi_id":"285025","summary":null,"start":178830269,"end":179050086,"strand":-1,"description":"coiled-coil domain containing 141 [Source:HGNC Symbol;Acc:HGNC:26821]"}, {"versioned_ensembl_gene_id":"ENSG00000223782.1","gene_symbol":"RPS21P8","gene_name":"ribosomal protein S21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39705]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873798","summary":null,"start":26977543,"end":26977789,"strand":1,"description":"ribosomal protein S21 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:39705]"}, {"versioned_ensembl_gene_id":"ENSG00000283579.1","gene_symbol":"AL160035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26965967,"end":26991996,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221818.8","gene_symbol":"EBF2","gene_name":"early B-cell factor 2 [Source:HGNC Symbol;Acc:HGNC:19090]","synonyms":"FLJ11500,COE2","biotype":"protein_coding","ncbi_id":"64641","summary":"The protein encoded by this gene belongs to the COE (Collier/Olf/EBF) family of non-basic, helix-loop-helix transcription factors that have a well conserved DNA binding domain. The COE family proteins play an important role in variety of developmental processes. Studies in mouse suggest that this gene may be involved in the differentiation of osteoblasts. [provided by RefSeq, Oct 2011]","start":25841730,"end":26045397,"strand":-1,"description":"early B-cell factor 2 [Source:HGNC Symbol;Acc:HGNC:19090]"}, {"versioned_ensembl_gene_id":"ENSG00000160781.15","gene_symbol":"PAQR6","gene_name":"progestin and adipoQ receptor family member 6 [Source:HGNC Symbol;Acc:HGNC:30132]","synonyms":"PRdelta,FLJ22672","biotype":"protein_coding","ncbi_id":"79957","summary":null,"start":156243321,"end":156248117,"strand":-1,"description":"progestin and adipoQ receptor family member 6 [Source:HGNC Symbol;Acc:HGNC:30132]"}, {"versioned_ensembl_gene_id":"ENSG00000196367.12","gene_symbol":"TRRAP","gene_name":"transformation/transcription domain associated protein [Source:HGNC Symbol;Acc:HGNC:12347]","synonyms":"Tra1,TR-AP,PAF400","biotype":"protein_coding","ncbi_id":"8295","summary":"This gene encodes a large multidomain protein of the phosphoinositide 3-kinase-related kinases (PIKK) family. The encoded protein is a common component of many histone acetyltransferase (HAT) complexes and plays a role in transcription and DNA repair by recruiting HAT complexes to chromatin. Deregulation of this gene may play a role in several types of cancer including glioblastoma multiforme. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]","start":98877933,"end":99013243,"strand":1,"description":"transformation/transcription domain associated protein [Source:HGNC Symbol;Acc:HGNC:12347]"}, {"versioned_ensembl_gene_id":"ENSG00000228231.2","gene_symbol":"AL589946.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54365335,"end":54369971,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169418.9","gene_symbol":"NPR1","gene_name":"natriuretic peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:7943]","synonyms":"NPRA,GUCY2A,ANPRA,ANPa","biotype":"protein_coding","ncbi_id":"4881","summary":"Guanylyl cyclases, catalyzing the production of cGMP from GTP, are classified as soluble and membrane forms (Garbers and Lowe, 1994 [PubMed 7982997]). The membrane guanylyl cyclases, often termed guanylyl cyclases A through F, form a family of cell-surface receptors with a similar topographic structure: an extracellular ligand-binding domain, a single membrane-spanning domain, and an intracellular region that contains a protein kinase-like domain and a cyclase catalytic domain. GC-A and GC-B function as receptors for natriuretic peptides; they are also referred to as atrial natriuretic peptide receptor A (NPR1) and type B (NPR2; MIM 108961). Also see NPR3 (MIM 108962), which encodes a protein with only the ligand-binding transmembrane and 37-amino acid cytoplasmic domains. NPR1 is a membrane-bound guanylate cyclase that serves as the receptor for both atrial and brain natriuretic peptides (ANP (MIM 108780) and BNP (MIM 600295), respectively).[supplied by OMIM, May 2009]","start":153678637,"end":153693992,"strand":1,"description":"natriuretic peptide receptor 1 [Source:HGNC Symbol;Acc:HGNC:7943]"}, {"versioned_ensembl_gene_id":"ENSG00000232718.1","gene_symbol":"GAPDHP48","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:37805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100240713","summary":null,"start":3688021,"end":3688981,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:37805]"}, {"versioned_ensembl_gene_id":"ENSG00000272636.3","gene_symbol":"DOC2B","gene_name":"double C2 domain beta [Source:HGNC Symbol;Acc:HGNC:2986]","synonyms":"DOC2BL","biotype":"protein_coding","ncbi_id":"8447","summary":"There are at least two protein isoforms of the Double C2 protein, namely alpha (DOC2A) and beta (DOC2B), which contain two C2-like domains. DOC2A and DOC2B are encoded by different genes; these genes are at times confused with the unrelated DAB2 gene which was initially named DOC-2. DOC2B is expressed ubiquitously and is suggested to be involved in Ca(2+)-dependent intracellular vesicle trafficking in various types of cells. [provided by RefSeq, Jul 2008]","start":142789,"end":181636,"strand":-1,"description":"double C2 domain beta [Source:HGNC Symbol;Acc:HGNC:2986]"}, {"versioned_ensembl_gene_id":"ENSG00000281989.1","gene_symbol":"AC239618.3","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142848110,"end":142848157,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230659.3","gene_symbol":"AL451074.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165819353,"end":165819787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227290.1","gene_symbol":"LINC01364","gene_name":"long intergenic non-protein coding RNA 1364 [Source:HGNC Symbol;Acc:HGNC:50599]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505768","summary":null,"start":87353524,"end":87371655,"strand":-1,"description":"long intergenic non-protein coding RNA 1364 [Source:HGNC Symbol;Acc:HGNC:50599]"}, {"versioned_ensembl_gene_id":"ENSG00000236364.3","gene_symbol":"AL358115.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165890795,"end":165900683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266578.1","gene_symbol":"AP001025.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3284145,"end":3327292,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213717.3","gene_symbol":"AC004692.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43274159,"end":43274582,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224358.1","gene_symbol":"AL451074.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":165768929,"end":165775176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282500.1","gene_symbol":"AC239618.9","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142848723,"end":142848772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229711.1","gene_symbol":"AL512366.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":50822692,"end":50824525,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225344.1","gene_symbol":"AL035252.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25161167,"end":25162061,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000002746.14","gene_symbol":"HECW1","gene_name":"HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:22195]","synonyms":"NEDL1,KIAA0322","biotype":"protein_coding","ncbi_id":"23072","summary":null,"start":43112599,"end":43566001,"strand":1,"description":"HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:22195]"}, {"versioned_ensembl_gene_id":"ENSG00000143179.14","gene_symbol":"UCK2","gene_name":"uridine-cytidine kinase 2 [Source:HGNC Symbol;Acc:HGNC:12562]","synonyms":"UMPK","biotype":"protein_coding","ncbi_id":"7371","summary":"This gene encodes a pyrimidine ribonucleoside kinase. The encoded protein (EC 2.7.1.48) catalyzes phosphorylation of uridine and cytidine to uridine monophosphate (UMP) and cytidine monophosphate (CMP), respectively.[provided by RefSeq, Oct 2010]","start":165827531,"end":165911618,"strand":1,"description":"uridine-cytidine kinase 2 [Source:HGNC Symbol;Acc:HGNC:12562]"}, {"versioned_ensembl_gene_id":"ENSG00000227422.1","gene_symbol":"DDR1-AS1","gene_name":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]","synonyms":"bPG70P20.2,TIGD1L,bCX111D4.7,bQB10J12.1","biotype":"processed_transcript","ncbi_id":"414771","summary":null,"start":30945549,"end":30954477,"strand":-1,"description":"DDR1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:28694]"}, {"versioned_ensembl_gene_id":"ENSG00000204147.9","gene_symbol":"ASAH2B","gene_name":"N-acylsphingosine amidohydrolase 2B [Source:HGNC Symbol;Acc:HGNC:23456]","synonyms":"bA98I6.3,bA449O16.3,ASAH2L,ASAH2C","biotype":"protein_coding","ncbi_id":"653308","summary":null,"start":50739318,"end":50816495,"strand":1,"description":"N-acylsphingosine amidohydrolase 2B [Source:HGNC Symbol;Acc:HGNC:23456]"}, {"versioned_ensembl_gene_id":"ENSG00000100038.19","gene_symbol":"TOP3B","gene_name":"topoisomerase (DNA) III beta [Source:HGNC Symbol;Acc:HGNC:11993]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8940","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus relaxing the supercoils and altering the topology of DNA. The enzyme interacts with DNA helicase SGS1 and plays a role in DNA recombination, cellular aging and maintenance of genome stability. Low expression of this gene may be related to higher survival rates in breast cancer patients. This gene has a pseudogene on chromosome 22. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Aug 2013]","start":21957025,"end":21982816,"strand":-1,"description":"topoisomerase (DNA) III beta [Source:HGNC Symbol;Acc:HGNC:11993]"}, {"versioned_ensembl_gene_id":"ENSG00000211753.4","gene_symbol":"TRBV28","gene_name":"T-cell receptor beta variable 28 [Source:HGNC Symbol;Acc:HGNC:12209]","synonyms":"TCRBV3S1,TCRBV28S1","biotype":"TR_V_gene","ncbi_id":"28559","summary":null,"start":142720660,"end":142721160,"strand":1,"description":"T-cell receptor beta variable 28 [Source:HGNC Symbol;Acc:HGNC:12209]"}, {"versioned_ensembl_gene_id":"ENSG00000276297.1","gene_symbol":"AC138832.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70660919,"end":70661872,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223543.1","gene_symbol":"TCEAL4P1","gene_name":"transcription elongation factor A like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39582]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874432","summary":null,"start":36741878,"end":36742465,"strand":-1,"description":"transcription elongation factor A like 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39582]"}, {"versioned_ensembl_gene_id":"ENSG00000275192.1","gene_symbol":"LINC02197","gene_name":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"102724392","summary":null,"start":70567180,"end":70661645,"strand":-1,"description":"long intergenic non-protein coding RNA 2197 [Source:HGNC Symbol;Acc:HGNC:53063]"}, {"versioned_ensembl_gene_id":"ENSG00000279778.1","gene_symbol":"AL445437.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87805286,"end":87808372,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244273.1","gene_symbol":"PGBD4P1","gene_name":"piggyBac transposable element derived 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107161154","summary":null,"start":142722358,"end":142722764,"strand":1,"description":"piggyBac transposable element derived 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44066]"}, {"versioned_ensembl_gene_id":"ENSG00000215486.5","gene_symbol":"ARL2BPP3","gene_name":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39447]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"646879","summary":null,"start":36789332,"end":36795050,"strand":1,"description":"ADP ribosylation factor like GTPase 2 binding protein pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39447]"}, {"versioned_ensembl_gene_id":"ENSG00000224235.1","gene_symbol":"LINC01773","gene_name":"long intergenic non-protein coding RNA 1773 [Source:HGNC Symbol;Acc:HGNC:52563]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985519","summary":null,"start":87899909,"end":87905714,"strand":-1,"description":"long intergenic non-protein coding RNA 1773 [Source:HGNC Symbol;Acc:HGNC:52563]"}, {"versioned_ensembl_gene_id":"ENSG00000277680.1","gene_symbol":"AC139463.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":70587997,"end":70590219,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271337.1","gene_symbol":"NDE1P2","gene_name":"nudE neurodevelopment protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49116]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480247","summary":null,"start":36804198,"end":36805302,"strand":-1,"description":"nudE neurodevelopment protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49116]"}, {"versioned_ensembl_gene_id":"ENSG00000275396.4","gene_symbol":"PMCHL2","gene_name":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"5370","summary":null,"start":70591107,"end":70601315,"strand":1,"description":"pro-melanin concentrating hormone like 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:9111]"}, {"versioned_ensembl_gene_id":"ENSG00000232869.2","gene_symbol":"TRBV29-1","gene_name":"T-cell receptor beta variable 29-1 [Source:HGNC Symbol;Acc:HGNC:12210]","synonyms":"TRBV291,TCRBV4S1A1T,TCRBV29S1","biotype":"TR_V_gene","ncbi_id":"28558","summary":null,"start":142740206,"end":142740894,"strand":1,"description":"T-cell receptor beta variable 29-1 [Source:HGNC Symbol;Acc:HGNC:12210]"}, {"versioned_ensembl_gene_id":"ENSG00000270507.1","gene_symbol":"AL049861.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88313153,"end":88313302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230053.2","gene_symbol":"AC093578.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88498309,"end":88498676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282273.1","gene_symbol":"AC239618.7","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142849318,"end":142849368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234131.1","gene_symbol":"ELOCP8","gene_name":"elongin C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38144]","synonyms":"TCEB1P8","biotype":"processed_pseudogene","ncbi_id":"100462869","summary":null,"start":22517242,"end":22517573,"strand":-1,"description":"elongin C pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:38144]"}, {"versioned_ensembl_gene_id":"ENSG00000259256.1","gene_symbol":"LINC01895","gene_name":"long intergenic non-protein coding RNA 1895 [Source:HGNC Symbol;Acc:HGNC:52714]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371964","summary":null,"start":3347776,"end":3350559,"strand":-1,"description":"long intergenic non-protein coding RNA 1895 [Source:HGNC Symbol;Acc:HGNC:52714]"}, {"versioned_ensembl_gene_id":"ENSG00000104312.7","gene_symbol":"RIPK2","gene_name":"receptor interacting serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:10020]","synonyms":"RIP2,RICK,CARDIAK,CARD3","biotype":"protein_coding","ncbi_id":"8767","summary":"This gene encodes a member of the receptor-interacting protein (RIP) family of serine/threonine protein kinases. The encoded protein contains a C-terminal caspase activation and recruitment domain (CARD), and is a component of signaling complexes in both the innate and adaptive immune pathways. It is a potent activator of NF-kappaB and inducer of apoptosis in response to various stimuli. [provided by RefSeq, Jul 2008]","start":89757747,"end":89791063,"strand":1,"description":"receptor interacting serine/threonine kinase 2 [Source:HGNC Symbol;Acc:HGNC:10020]"}, {"versioned_ensembl_gene_id":"ENSG00000282215.1","gene_symbol":"AC239618.5","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142849591,"end":142849640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270277.1","gene_symbol":"AC009948.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178548884,"end":178550681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267784.1","gene_symbol":"AC010680.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178723457,"end":178727046,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270956.1","gene_symbol":"AC009948.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178541125,"end":178541799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107159.12","gene_symbol":"CA9","gene_name":"carbonic anhydrase 9 [Source:HGNC Symbol;Acc:HGNC:1383]","synonyms":"MN,CAIX","biotype":"protein_coding","ncbi_id":"768","summary":"Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA IX is a transmembrane protein and is one of only two tumor-associated carbonic anhydrase isoenzymes known. It is expressed in all clear-cell renal cell carcinoma, but is not detected in normal kidney or most other normal tissues. It may be involved in cell proliferation and transformation. This gene was mapped to 17q21.2 by fluorescence in situ hybridization, however, radiation hybrid mapping localized it to 9p13-p12. [provided by RefSeq, Jun 2014]","start":35673856,"end":35681159,"strand":1,"description":"carbonic anhydrase 9 [Source:HGNC Symbol;Acc:HGNC:1383]"}, {"versioned_ensembl_gene_id":"ENSG00000176797.3","gene_symbol":"DEFB103A","gene_name":"defensin beta 103A [Source:HGNC Symbol;Acc:HGNC:15967]","synonyms":"HBD3,HBD-3,DEFB3,DEFB103,DEFB-3,HBP3,HBP-3","biotype":"protein_coding","ncbi_id":"414325","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 103, an antibiotic peptide which is induced by bacteria and interferon gamma, and which displays antimicrobial activity against S. aureus, S. pyogenes, P. aeruginosa, E. coli, and C. albicans. [provided by RefSeq, Oct 2014]","start":7881204,"end":7882664,"strand":1,"description":"defensin beta 103A [Source:HGNC Symbol;Acc:HGNC:15967]"}, {"versioned_ensembl_gene_id":"ENSG00000224873.1","gene_symbol":"CDY13P","gene_name":"chromodomain Y-linked 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:23857]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"386735","summary":null,"start":22520681,"end":22521695,"strand":-1,"description":"chromodomain Y-linked 13 pseudogene [Source:HGNC Symbol;Acc:HGNC:23857]"}, {"versioned_ensembl_gene_id":"ENSG00000250200.1","gene_symbol":"AC105914.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":174923813,"end":174924038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231541.1","gene_symbol":"RPS6P2","gene_name":"ribosomal protein S6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36446]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270864","summary":null,"start":179001756,"end":179002760,"strand":1,"description":"ribosomal protein S6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:36446]"}, {"versioned_ensembl_gene_id":"ENSG00000250431.1","gene_symbol":"AC105914.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":174977571,"end":174979381,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230814.1","gene_symbol":"USP9YP24","gene_name":"ubiquitin specific peptidase 9, Y-linked pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:38760]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478928","summary":null,"start":22528281,"end":22536639,"strand":1,"description":"ubiquitin specific peptidase 9, Y-linked pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:38760]"}, {"versioned_ensembl_gene_id":"ENSG00000248399.1","gene_symbol":"AL645924.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":2463797,"end":2464124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260217.1","gene_symbol":"AC104640.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175938929,"end":175941037,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281580.2","gene_symbol":"LINC01060","gene_name":"long intergenic non-protein coding RNA 1060 [Source:HGNC Symbol;Acc:HGNC:49081]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401164","summary":null,"start":188400736,"end":188543559,"strand":1,"description":"long intergenic non-protein coding RNA 1060 [Source:HGNC Symbol;Acc:HGNC:49081]"}, {"versioned_ensembl_gene_id":"ENSG00000281026.1","gene_symbol":"N4BP2L2-IT2","gene_name":"N4BPL2 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:25038]","synonyms":"CG030","biotype":"sense_intronic","ncbi_id":"116828","summary":null,"start":32504506,"end":32509395,"strand":-1,"description":"N4BPL2 intronic transcript 2 [Source:HGNC Symbol;Acc:HGNC:25038]"}, {"versioned_ensembl_gene_id":"ENSG00000168594.15","gene_symbol":"ADAM29","gene_name":"ADAM metallopeptidase domain 29 [Source:HGNC Symbol;Acc:HGNC:207]","synonyms":"svph1,CT73","biotype":"protein_coding","ncbi_id":"11086","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene is highly expressed in testis and may be involved in human spermatogenesis. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Jul 2008]","start":174829668,"end":174978180,"strand":1,"description":"ADAM metallopeptidase domain 29 [Source:HGNC Symbol;Acc:HGNC:207]"}, {"versioned_ensembl_gene_id":"ENSG00000228571.1","gene_symbol":"HSFY7P","gene_name":"heat shock transcription factor, Y-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:38791]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106478935","summary":null,"start":22537047,"end":22537849,"strand":1,"description":"heat shock transcription factor, Y-linked 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:38791]"}, {"versioned_ensembl_gene_id":"ENSG00000148584.14","gene_symbol":"A1CF","gene_name":"APOBEC1 complementation factor [Source:HGNC Symbol;Acc:HGNC:24086]","synonyms":"ASP,APOBEC1CF,ACF65,ACF64,ACF","biotype":"protein_coding","ncbi_id":"29974","summary":"Mammalian apolipoprotein B mRNA undergoes site-specific C to U deamination, which is mediated by a multi-component enzyme complex containing a minimal core composed of APOBEC-1 and a complementation factor encoded by this gene. The gene product has three non-identical RNA recognition motifs and belongs to the hnRNP R family of RNA-binding proteins. It has been proposed that this complementation factor functions as an RNA-binding subunit and docks APOBEC-1 to deaminate the upstream cytidine. Studies suggest that the protein may also be involved in other RNA editing or RNA processing events. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]","start":50799409,"end":50885675,"strand":-1,"description":"APOBEC1 complementation factor [Source:HGNC Symbol;Acc:HGNC:24086]"}, {"versioned_ensembl_gene_id":"ENSG00000240364.1","gene_symbol":"AP001025.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3377916,"end":3378247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241975.1","gene_symbol":"ELOCP19","gene_name":"elongin C pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38155]","synonyms":"TCEB1P19","biotype":"processed_pseudogene","ncbi_id":"100462880","summary":null,"start":88829102,"end":88829419,"strand":1,"description":"elongin C pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:38155]"}, {"versioned_ensembl_gene_id":"ENSG00000282058.1","gene_symbol":"AC138749.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28557532,"end":28561397,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065243.19","gene_symbol":"PKN2","gene_name":"protein kinase N2 [Source:HGNC Symbol;Acc:HGNC:9406]","synonyms":"STK7,PRKCL2,PRK2,Pak-2","biotype":"protein_coding","ncbi_id":"5586","summary":null,"start":88684222,"end":88836255,"strand":1,"description":"protein kinase N2 [Source:HGNC Symbol;Acc:HGNC:9406]"}, {"versioned_ensembl_gene_id":"ENSG00000281957.1","gene_symbol":"AC239618.1","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142850081,"end":142850133,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281276.1","gene_symbol":"AP000351.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23987324,"end":23991428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278444.1","gene_symbol":"CDC42EP5","gene_name":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]","synonyms":"Borg3,CEP5","biotype":"protein_coding","ncbi_id":"148170","summary":"Cell division control protein 42 (CDC42), a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to CDC42 and regulate its function negatively. The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding. The protein may also play a role in septin organization and inducing pseudopodia formation in fibroblasts [provided by RefSeq, Jul 2013]","start":54472957,"end":54481158,"strand":-1,"description":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]"}, {"versioned_ensembl_gene_id":"ENSG00000116014.9","gene_symbol":"KISS1R","gene_name":"KISS1 receptor [Source:HGNC Symbol;Acc:HGNC:4510]","synonyms":"HOT7T175,GPR54,AXOR12","biotype":"protein_coding","ncbi_id":"84634","summary":"The protein encoded by this gene is a galanin-like G protein-coupled receptor that binds metastin, a peptide encoded by the metastasis suppressor gene KISS1. The tissue distribution of the expressed gene suggests that it is involved in the regulation of endocrine function, and this is supported by the finding that this gene appears to play a role in the onset of puberty. Mutations in this gene have been associated with hypogonadotropic hypogonadism and central precocious puberty. [provided by RefSeq, Jul 2008]","start":917287,"end":921015,"strand":1,"description":"KISS1 receptor [Source:HGNC Symbol;Acc:HGNC:4510]"}, {"versioned_ensembl_gene_id":"ENSG00000214782.7","gene_symbol":"AP004243.1","gene_name":"Membrane-spanning 4-domains subfamily A member 18 [Source:UniProtKB/Swiss-Prot;Acc:Q3C1V0]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":60729304,"end":60744212,"strand":1,"description":"Membrane-spanning 4-domains subfamily A member 18 [Source:UniProtKB/Swiss-Prot;Acc:Q3C1V0]"}, {"versioned_ensembl_gene_id":"ENSG00000280330.1","gene_symbol":"CU634019.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7129103,"end":7130287,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279303.1","gene_symbol":"CU634019.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":7135334,"end":7137789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281981.2","gene_symbol":"AC239618.2","gene_name":null,"synonyms":null,"biotype":"TR_C_gene","ncbi_id":null,"summary":null,"start":142852787,"end":142854461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219549.1","gene_symbol":"AL607077.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":95630115,"end":95632929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279647.1","gene_symbol":"CU633904.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7385058,"end":7388799,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254543.1","gene_symbol":"AC130365.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7891003,"end":7892555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265243.1","gene_symbol":"IGLJCOR18","gene_name":"immunoglobulin lambda joining-constant/OR18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28614]","synonyms":"IGLJ-COR18,IGLJ-C/OR18","biotype":"IG_C_pseudogene","ncbi_id":"204777","summary":null,"start":3394889,"end":3395312,"strand":1,"description":"immunoglobulin lambda joining-constant/OR18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:28614]"}, {"versioned_ensembl_gene_id":"ENSG00000155657.26","gene_symbol":"TTN","gene_name":"titin [Source:HGNC Symbol;Acc:HGNC:12403]","synonyms":"FLJ32040,CMPD4,CMH9,CMD1G,TMD,MYLK5,LGMD2J","biotype":"protein_coding","ncbi_id":"7273","summary":"This gene encodes a large abundant protein of striated muscle. The product of this gene is divided into two regions, a N-terminal I-band and a C-terminal A-band. The I-band, which is the elastic part of the molecule, contains two regions of tandem immunoglobulin domains on either side of a PEVK region that is rich in proline, glutamate, valine and lysine. The A-band, which is thought to act as a protein-ruler, contains a mixture of immunoglobulin and fibronectin repeats, and possesses kinase activity. An N-terminal Z-disc region and a C-terminal M-line region bind to the Z-line and M-line of the sarcomere, respectively, so that a single titin molecule spans half the length of a sarcomere. Titin also contains binding sites for muscle associated proteins so it serves as an adhesion template for the assembly of contractile machinery in muscle cells. It has also been identified as a structural protein for chromosomes. Alternative splicing of this gene results in multiple transcript variants. Considerable variability exists in the I-band, the M-line and the Z-disc regions of titin. Variability in the I-band region contributes to the differences in elasticity of different titin isoforms and, therefore, to the differences in elasticity of different muscle types. Mutations in this gene are associated with familial hypertrophic cardiomyopathy 9, and autoantibodies to titin are produced in patients with the autoimmune disease scleroderma. [provided by RefSeq, Feb 2012]","start":178525989,"end":178830802,"strand":-1,"description":"titin [Source:HGNC Symbol;Acc:HGNC:12403]"}, {"versioned_ensembl_gene_id":"ENSG00000231424.2","gene_symbol":"AL445673.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":171247580,"end":171251794,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281748.3","gene_symbol":"GSTTP1","gene_name":"glutathione S-transferase theta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26930]","synonyms":"HS322B1A","biotype":"protein_coding","ncbi_id":"25774","summary":null,"start":23998411,"end":24005163,"strand":-1,"description":"glutathione S-transferase theta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:26930]"}, {"versioned_ensembl_gene_id":"ENSG00000232241.1","gene_symbol":"DYNLT3P1","gene_name":"dynein light chain Tctex-type 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16571]","synonyms":"TCTE1P,dJ531H16.2","biotype":"processed_pseudogene","ncbi_id":"170554","summary":null,"start":17479085,"end":17479431,"strand":-1,"description":"dynein light chain Tctex-type 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16571]"}, {"versioned_ensembl_gene_id":"ENSG00000101745.16","gene_symbol":"ANKRD12","gene_name":"ankyrin repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:29135]","synonyms":"KIAA0874,GAC-1,FLJ20053","biotype":"protein_coding","ncbi_id":"23253","summary":"This gene encodes a member of the ankyrin repeats-containing cofactor family. These proteins may inhibit the transcriptional activity of nuclear receptors through the recruitment of histone deacetylases. The encoded protein interacts with p160 coactivators and also represses transcription mediated by the coactivator alteration/deficiency in activation 3 (ADA3). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]","start":9136228,"end":9285985,"strand":1,"description":"ankyrin repeat domain 12 [Source:HGNC Symbol;Acc:HGNC:29135]"}, {"versioned_ensembl_gene_id":"ENSG00000150712.10","gene_symbol":"MTMR12","gene_name":"myotubularin related protein 12 [Source:HGNC Symbol;Acc:HGNC:18191]","synonyms":"3PAP,3-PAP,PIP3AP,KIAA1682,FLJ20476","biotype":"protein_coding","ncbi_id":"54545","summary":"Phosphatidylinositide 3-kinase-derived membrane-anchored phosphatidylinositides, such as phosphatidylinositol 3-phosphate (PtdIns(3)P), regulate diverse cellular processes. The protein encoded by this gene functions as an adaptor subunit in a complex with an active PtdIns(3)P 3-phosphatase. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":32226994,"end":32313009,"strand":-1,"description":"myotubularin related protein 12 [Source:HGNC Symbol;Acc:HGNC:18191]"}, {"versioned_ensembl_gene_id":"ENSG00000148604.13","gene_symbol":"RGR","gene_name":"retinal G protein coupled receptor [Source:HGNC Symbol;Acc:HGNC:9990]","synonyms":"RP44","biotype":"protein_coding","ncbi_id":"5995","summary":"This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":84245053,"end":84259960,"strand":1,"description":"retinal G protein coupled receptor [Source:HGNC Symbol;Acc:HGNC:9990]"}, {"versioned_ensembl_gene_id":"ENSG00000063978.15","gene_symbol":"RNF4","gene_name":"ring finger protein 4 [Source:HGNC Symbol;Acc:HGNC:10067]","synonyms":"SNURF,SLX5,RES4-26","biotype":"protein_coding","ncbi_id":"6047","summary":"The protein encoded by this gene contains a RING finger motif and acts as a transcription regulator. This protein has been shown to interact with, and inhibit the activity of, TRPS1, a transcription suppressor of GATA-mediated transcription. Transcription repressor ZNF278/PATZ is found to interact with this protein, and thus reduce the enhancement of androgen receptor-dependent transcription mediated by this protein. Studies of the mouse and rat counterparts suggested a role of this protein in spermatogenesis. A pseudogene of this gene is found on chromosome 1.[provided by RefSeq, Jul 2010]","start":2462220,"end":2625320,"strand":1,"description":"ring finger protein 4 [Source:HGNC Symbol;Acc:HGNC:10067]"}, {"versioned_ensembl_gene_id":"ENSG00000276485.2","gene_symbol":"AC138749.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28565258,"end":28572999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174407.13","gene_symbol":"MIR1-1HG","gene_name":"MIR1-1 host gene [Source:HGNC Symbol;Acc:HGNC:16159]","synonyms":"MIR133A2HG,dJ353C17.1,C20orf166","biotype":"antisense_RNA","ncbi_id":"128826","summary":null,"start":62550453,"end":62570764,"strand":1,"description":"MIR1-1 host gene [Source:HGNC Symbol;Acc:HGNC:16159]"}, {"versioned_ensembl_gene_id":"ENSG00000102172.15","gene_symbol":"SMS","gene_name":"spermine synthase [Source:HGNC Symbol;Acc:HGNC:11123]","synonyms":"SRS,SpS,SPMSY,MRSR","biotype":"protein_coding","ncbi_id":"6611","summary":"This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]","start":21940573,"end":21994835,"strand":1,"description":"spermine synthase [Source:HGNC Symbol;Acc:HGNC:11123]"}, {"versioned_ensembl_gene_id":"ENSG00000282488.1","gene_symbol":"TRBJ2-1","gene_name":"T-cell receptor beta joining 2-1 [Source:HGNC Symbol;Acc:HGNC:12168]","synonyms":"TRBJ21,TCRBJ2S1","biotype":"TR_J_gene","ncbi_id":"28629","summary":null,"start":142857458,"end":142857507,"strand":1,"description":"T-cell receptor beta joining 2-1 [Source:HGNC Symbol;Acc:HGNC:12168]"}, {"versioned_ensembl_gene_id":"ENSG00000243720.1","gene_symbol":"AP001025.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":3406342,"end":3406818,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171711.2","gene_symbol":"DEFB4A","gene_name":"defensin beta 4A [Source:HGNC Symbol;Acc:HGNC:2767]","synonyms":"SAP1,HBD-2,DEFB4,DEFB2,DEFB102,DEFB-2","biotype":"protein_coding","ncbi_id":"1673","summary":"Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 4, an antibiotic peptide which is locally regulated by inflammation. [provided by RefSeq, Jul 2008]","start":7894629,"end":7896711,"strand":1,"description":"defensin beta 4A [Source:HGNC Symbol;Acc:HGNC:2767]"}, {"versioned_ensembl_gene_id":"ENSG00000162613.16","gene_symbol":"FUBP1","gene_name":"far upstream element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4004]","synonyms":"FUBP,FBP","biotype":"protein_coding","ncbi_id":"8880","summary":"The protein encoded by this gene is a single stranded DNA-binding protein that binds to multiple DNA elements, including the far upstream element (FUSE) located upstream of c-myc. Binding to FUSE occurs on the non-coding strand, and is important to the regulation of c-myc in undifferentiated cells. This protein contains three domains, an amphipathic helix N-terminal domain, a DNA-binding central domain, and a C-terminal transactivation domain that contains three tyrosine-rich motifs. The N-terminal domain is thought to repress the activity of the C-terminal domain. This protein is also thought to bind RNA, and contains 3'-5' helicase activity with in vitro activity on both DNA-DNA and RNA-RNA duplexes. Aberrant expression of this gene has been found in malignant tissues, and this gene is important to neural system and lung development. Binding of this protein to viral RNA is thought to play a role in several viral diseases, including hepatitis C and hand, foot and mouth disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":77944055,"end":77979110,"strand":-1,"description":"far upstream element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4004]"}, {"versioned_ensembl_gene_id":"ENSG00000159884.11","gene_symbol":"CCDC107","gene_name":"coiled-coil domain containing 107 [Source:HGNC Symbol;Acc:HGNC:28465]","synonyms":"MGC31967","biotype":"protein_coding","ncbi_id":"203260","summary":"This gene encodes a membrane protein which contains a coiled-coil domain in the central region. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013]","start":35658290,"end":35661511,"strand":1,"description":"coiled-coil domain containing 107 [Source:HGNC Symbol;Acc:HGNC:28465]"}, {"versioned_ensembl_gene_id":"ENSG00000174403.15","gene_symbol":"C20orf166-AS1","gene_name":"C20orf166 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26393]","synonyms":"NCRNA00335,FLJ30313,C20orf200","biotype":"antisense_RNA","ncbi_id":"253868","summary":null,"start":62544343,"end":62551526,"strand":-1,"description":"C20orf166 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26393]"}, {"versioned_ensembl_gene_id":"ENSG00000227262.3","gene_symbol":"HCG4B","gene_name":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]","synonyms":"HCGIV-6,bPG309N1.1,Em:AB023056.16,HCGIV-06,HCGIV.5,bCX67J3.3,bQB90C11.3,HCG4P6","biotype":"unprocessed_pseudogene","ncbi_id":"80868","summary":null,"start":29925983,"end":29926973,"strand":-1,"description":"HLA complex group 4B (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:22919]"}, {"versioned_ensembl_gene_id":"ENSG00000230521.1","gene_symbol":"AL645929.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29887294,"end":29888268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280470.1","gene_symbol":"CEACAMP3","gene_name":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]","synonyms":"CGM10,CEACAM24P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"1092","summary":null,"start":41608077,"end":41614326,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:1825]"}, {"versioned_ensembl_gene_id":"ENSG00000206341.7","gene_symbol":"HLA-H","gene_name":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"3136","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010]","start":29887752,"end":29890482,"strand":1,"description":"major histocompatibility complex, class I, H (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4965]"}, {"versioned_ensembl_gene_id":"ENSG00000204623.9","gene_symbol":"ZNRD1ASP","gene_name":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]","synonyms":"Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,Em:AB023056.3,HCGVIII,HTEX4,ZNRD1-AS,ZNRD1AS,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1,C6orf12,HCG8,HCGVIII-1,NCRNA00171,ZNRD1-AS1","biotype":"transcribed_unitary_pseudogene","ncbi_id":"80862","summary":null,"start":30001011,"end":30061640,"strand":-1,"description":"zinc ribbon domain containing 1 antisense, pseudogene [Source:HGNC Symbol;Acc:HGNC:13924]"}, {"versioned_ensembl_gene_id":"ENSG00000282272.1","gene_symbol":"TRBJ2-2","gene_name":"T-cell receptor beta joining 2-2 [Source:HGNC Symbol;Acc:HGNC:12169]","synonyms":"TRBJ22,TCRBJ2S2","biotype":"TR_J_gene","ncbi_id":"28628","summary":null,"start":142857653,"end":142857703,"strand":1,"description":"T-cell receptor beta joining 2-2 [Source:HGNC Symbol;Acc:HGNC:12169]"}, {"versioned_ensembl_gene_id":"ENSG00000133111.3","gene_symbol":"RFXAP","gene_name":"regulatory factor X associated protein [Source:HGNC Symbol;Acc:HGNC:9988]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5994","summary":"Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated ankyrin-containing protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group D. Transcript variants utilizing different polyA signals have been found for this gene. [provided by RefSeq, Jul 2008]","start":36819224,"end":36829104,"strand":1,"description":"regulatory factor X associated protein [Source:HGNC Symbol;Acc:HGNC:9988]"}, {"versioned_ensembl_gene_id":"ENSG00000282531.1","gene_symbol":"AC138749.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28576608,"end":28576845,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230944.1","gene_symbol":"AC026202.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5255535,"end":5256761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280929.1","gene_symbol":"AP000351.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24008537,"end":24009893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101363.12","gene_symbol":"MANBAL","gene_name":"mannosidase beta like [Source:HGNC Symbol;Acc:HGNC:15799]","synonyms":"dJ1141E15.2","biotype":"protein_coding","ncbi_id":"63905","summary":null,"start":37289638,"end":37317260,"strand":1,"description":"mannosidase beta like [Source:HGNC Symbol;Acc:HGNC:15799]"}, {"versioned_ensembl_gene_id":"ENSG00000230362.1","gene_symbol":"ACTG1P23","gene_name":"actin gamma 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51503]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442097","summary":null,"start":175977497,"end":175978570,"strand":-1,"description":"actin gamma 1 pseudogene 23 [Source:HGNC Symbol;Acc:HGNC:51503]"}, {"versioned_ensembl_gene_id":"ENSG00000282589.1","gene_symbol":"TRBJ2-2P","gene_name":"T-cell receptor beta joining 2-2P (non-functional) [Source:HGNC Symbol;Acc:HGNC:12170]","synonyms":"TRBJ22P","biotype":"TR_J_gene","ncbi_id":"28627","summary":null,"start":142857790,"end":142857835,"strand":1,"description":"T-cell receptor beta joining 2-2P (non-functional) [Source:HGNC Symbol;Acc:HGNC:12170]"}, {"versioned_ensembl_gene_id":"ENSG00000229642.1","gene_symbol":"AC087857.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5962842,"end":6124120,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236357.1","gene_symbol":"EI24P1","gene_name":"EI24, autophagy associated transmembrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44586]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129423","summary":null,"start":176068042,"end":176068908,"strand":-1,"description":"EI24, autophagy associated transmembrane protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44586]"}, {"versioned_ensembl_gene_id":"ENSG00000282090.1","gene_symbol":"HERC2P11","gene_name":"hect domain and RLD 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49882]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996738","summary":null,"start":28586639,"end":28591020,"strand":-1,"description":"hect domain and RLD 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49882]"}, {"versioned_ensembl_gene_id":"ENSG00000226094.1","gene_symbol":"RPL7P3","gene_name":"ribosomal protein L7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16566]","synonyms":"dJ353C17.2","biotype":"processed_pseudogene","ncbi_id":"140857","summary":null,"start":62572671,"end":62573384,"strand":1,"description":"ribosomal protein L7 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:16566]"}, {"versioned_ensembl_gene_id":"ENSG00000271413.1","gene_symbol":"AC104640.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176069107,"end":176069252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251452.2","gene_symbol":"AC109811.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":144920713,"end":144921164,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276636.2","gene_symbol":"AP000351.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24024565,"end":24028697,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232958.1","gene_symbol":"AC027119.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":6208269,"end":6208571,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164164.15","gene_symbol":"OTUD4","gene_name":"OTU deubiquitinase 4 [Source:HGNC Symbol;Acc:HGNC:24949]","synonyms":"DUBA6,KIAA1046,HSHIN1","biotype":"protein_coding","ncbi_id":"54726","summary":"Alternatively spliced transcript variants have been found for this gene. The smaller protein isoform encoded by the shorter transcript variant is found only in HIV-1 infected cells. [provided by RefSeq, Jul 2010]","start":145110838,"end":145180161,"strand":-1,"description":"OTU deubiquitinase 4 [Source:HGNC Symbol;Acc:HGNC:24949]"}, {"versioned_ensembl_gene_id":"ENSG00000075426.11","gene_symbol":"FOSL2","gene_name":"FOS like 2, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3798]","synonyms":"FRA2,FLJ23306","biotype":"protein_coding","ncbi_id":"2355","summary":"The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2. These genes encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. As such, the FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation. [provided by RefSeq, Jul 2014]","start":28392448,"end":28417312,"strand":1,"description":"FOS like 2, AP-1 transcription factor subunit [Source:HGNC Symbol;Acc:HGNC:3798]"}, {"versioned_ensembl_gene_id":"ENSG00000226022.1","gene_symbol":"AC026167.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6148484,"end":6365885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237819.5","gene_symbol":"AC002454.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92836483,"end":92917187,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230914.3","gene_symbol":"AC004840.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":2383698,"end":2388652,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282371.1","gene_symbol":"TRBJ2-3","gene_name":"T-cell receptor beta joining 2-3 [Source:HGNC Symbol;Acc:HGNC:12171]","synonyms":"TRBJ23,TCRBJ2S3","biotype":"TR_J_gene","ncbi_id":"28626","summary":null,"start":142857940,"end":142857988,"strand":1,"description":"T-cell receptor beta joining 2-3 [Source:HGNC Symbol;Acc:HGNC:12171]"}, {"versioned_ensembl_gene_id":"ENSG00000105810.9","gene_symbol":"CDK6","gene_name":"cyclin dependent kinase 6 [Source:HGNC Symbol;Acc:HGNC:1777]","synonyms":"PLSTIRE","biotype":"protein_coding","ncbi_id":"1021","summary":"The protein encoded by this gene is a member of the CMGC family of serine/threonine protein kinases. This kinase is a catalytic subunit of the protein kinase complex that is important for cell cycle G1 phase progression and G1/S transition. The activity of this kinase first appears in mid-G1 phase, which is controlled by the regulatory subunits including D-type cyclins and members of INK4 family of CDK inhibitors. This kinase, as well as CDK4, has been shown to phosphorylate, and thus regulate the activity of, tumor suppressor protein Rb. Altered expression of this gene has been observed in multiple human cancers. A mutation in this gene resulting in reduced cell proliferation, and impaired cell motility and polarity, and has been identified in patients with primary microcephaly. [provided by RefSeq, Aug 2017]","start":92604921,"end":92836594,"strand":-1,"description":"cyclin dependent kinase 6 [Source:HGNC Symbol;Acc:HGNC:1777]"}, {"versioned_ensembl_gene_id":"ENSG00000242038.5","gene_symbol":"EGFL8","gene_name":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]","synonyms":"C6orf8,NG3","biotype":"protein_coding","ncbi_id":"80864","summary":null,"start":32113054,"end":32116752,"strand":1,"description":"EGF like domain multiple 8 [Source:HGNC Symbol;Acc:HGNC:13944]"}, {"versioned_ensembl_gene_id":"ENSG00000103489.11","gene_symbol":"XYLT1","gene_name":"xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15516]","synonyms":"XT-I,PXYLT1","biotype":"protein_coding","ncbi_id":"64131","summary":"This locus encodes a xylosyltransferase enzyme. The encoded protein catalyzes transfer of UDP-xylose to serine residues of an acceptor protein substrate. This transfer reaction is necessary for biosynthesis of glycosaminoglycan chains. Mutations in this gene have been associated with increased severity of pseudoxanthoma elasticum.[provided by RefSeq, Nov 2009]","start":17101769,"end":17470881,"strand":-1,"description":"xylosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:15516]"}, {"versioned_ensembl_gene_id":"ENSG00000277335.4","gene_symbol":"LAIR2","gene_name":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]","synonyms":"CD306","biotype":"protein_coding","ncbi_id":"3904","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1, a membrane-bound receptor that modulates innate immune response. The protein encoded by this locus is a soluble receptor that may play roles in both inhibition of collagen-induced platelet aggregation and vessel formation during placental implantation. This gene maps to a region of 19q13.4, termed the leukocyte receptor cluster, which contains 29 genes in the immunoglobulin superfamily. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":54505847,"end":54518644,"strand":1,"description":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]"}, {"versioned_ensembl_gene_id":"ENSG00000107719.8","gene_symbol":"PALD1","gene_name":"phosphatase domain containing, paladin 1 [Source:HGNC Symbol;Acc:HGNC:23530]","synonyms":"PALD,KIAA1274","biotype":"protein_coding","ncbi_id":"27143","summary":null,"start":70478821,"end":70568449,"strand":1,"description":"phosphatase domain containing, paladin 1 [Source:HGNC Symbol;Acc:HGNC:23530]"}, {"versioned_ensembl_gene_id":"ENSG00000260592.1","gene_symbol":"AC130456.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19476916,"end":19487899,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260681.1","gene_symbol":"AC130456.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19410729,"end":19411662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280545.1","gene_symbol":"AC243960.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41648001,"end":41648944,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100196.10","gene_symbol":"KDELR3","gene_name":"KDEL endoplasmic reticulum protein retention receptor 3 [Source:HGNC Symbol;Acc:HGNC:6306]","synonyms":null,"biotype":"protein_coding","ncbi_id":"11015","summary":"This gene encodes a member of the KDEL endoplasmic reticulum protein retention receptor family. Retention of resident soluble proteins in the lumen of the endoplasmic reticulum (ER) is achieved in both yeast and animal cells by their continual retrieval from the cis-Golgi, or a pre-Golgi compartment. Sorting of these proteins is dependent on a C-terminal tetrapeptide signal, usually lys-asp-glu-leu (KDEL) in animal cells, and his-asp-glu-leu (HDEL) in S. cerevisiae. This process is mediated by a receptor that recognizes, and binds the tetrapeptide-containing protein, and returns it to the ER. In yeast, the sorting receptor encoded by a single gene, ERD2, is a seven-transmembrane protein. Unlike yeast, several human homologs of the ERD2 gene, constituting the KDEL receptor gene family, have been described. KDELR3 was the third member of the family to be identified. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":38468062,"end":38483447,"strand":1,"description":"KDEL endoplasmic reticulum protein retention receptor 3 [Source:HGNC Symbol;Acc:HGNC:6306]"}, {"versioned_ensembl_gene_id":"ENSG00000270640.1","gene_symbol":"AC104695.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":28396815,"end":28397110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281659.1","gene_symbol":"DNAJC19P3","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861443","summary":null,"start":41646911,"end":41647241,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:45066]"}, {"versioned_ensembl_gene_id":"ENSG00000229951.5","gene_symbol":"FLJ31356","gene_name":"uncharacterized protein FLJ31356 [Source:NCBI gene;Acc:403150]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"403150","summary":null,"start":28384409,"end":28394672,"strand":-1,"description":"uncharacterized protein FLJ31356 [Source:NCBI gene;Acc:403150]"}, {"versioned_ensembl_gene_id":"ENSG00000274131.3","gene_symbol":"CEACAM4","gene_name":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]","synonyms":"CGM7","biotype":"protein_coding","ncbi_id":"1089","summary":null,"start":41627313,"end":41635416,"strand":-1,"description":"carcinoembryonic antigen related cell adhesion molecule 4 [Source:HGNC Symbol;Acc:HGNC:1816]"}, {"versioned_ensembl_gene_id":"ENSG00000270457.1","gene_symbol":"AC093424.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":59289303,"end":59289640,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228128.6","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31717799,"end":31721378,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000237699.1","gene_symbol":"BX072579.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113877608,"end":113879376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279620.1","gene_symbol":"AC099494.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17249674,"end":17251395,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274766.1","gene_symbol":"BX072579.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":113883667,"end":113885335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261448.1","gene_symbol":"AC109446.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17134504,"end":17138736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279410.1","gene_symbol":"AC099494.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17192863,"end":17194232,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226921.6","gene_symbol":"LINC00454","gene_name":"long intergenic non-protein coding RNA 454 [Source:HGNC Symbol;Acc:HGNC:42802]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874178","summary":null,"start":113878489,"end":113883651,"strand":-1,"description":"long intergenic non-protein coding RNA 454 [Source:HGNC Symbol;Acc:HGNC:42802]"}, {"versioned_ensembl_gene_id":"ENSG00000275927.1","gene_symbol":"AC009152.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17445825,"end":17446380,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189091.12","gene_symbol":"SF3B3","gene_name":"splicing factor 3b subunit 3 [Source:HGNC Symbol;Acc:HGNC:10770]","synonyms":"SF3b130,SAP130,RSE1,KIAA0017","biotype":"protein_coding","ncbi_id":"23450","summary":"This gene encodes subunit 3 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence independent manner and may anchor the U2 snRNP to the pre-mRNA. Splicing factor 3b is also a component of the minor U12-type spliceosome. Subunit 3 has also been identified as a component of the STAGA (SPT3-TAF(II)31-GCN5L acetylase) transcription coactivator-HAT (histone acetyltransferase) complex, and the TFTC (TATA-binding-protein-free TAF(II)-containing complex). These complexes may function in chromatin modification, transcription, splicing, and DNA repair. [provided by RefSeq, Jul 2008]","start":70523788,"end":70577670,"strand":1,"description":"splicing factor 3b subunit 3 [Source:HGNC Symbol;Acc:HGNC:10770]"}, {"versioned_ensembl_gene_id":"ENSG00000279415.1","gene_symbol":"AC099494.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17227023,"end":17228000,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163785.12","gene_symbol":"RYK","gene_name":"receptor-like tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:10481]","synonyms":"RYK1,JTK5A,JTK5,D3S3195","biotype":"protein_coding","ncbi_id":"6259","summary":"The protein encoded by this gene is an atypical member of the family of growth factor receptor protein tyrosine kinases, differing from other members at a number of conserved residues in the activation and nucleotide binding domains. This gene product belongs to a subfamily whose members do not appear to be regulated by phosphorylation in the activation segment. It has been suggested that mediation of biological activity by recruitment of a signaling-competent auxiliary protein may occur through an as yet uncharacterized mechanism. The encoded protein has a leucine-rich extracellular domain with a WIF-type Wnt binding region, a single transmembrane domain, and an intracellular tyrosine kinase domain. This protein is involved in stimulating Wnt signaling pathways such as the regulation of axon pathfinding. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2012]","start":134065303,"end":134250744,"strand":-1,"description":"receptor-like tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:10481]"}, {"versioned_ensembl_gene_id":"ENSG00000281505.1","gene_symbol":"DNAJC19P2","gene_name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861445","summary":null,"start":41613683,"end":41614013,"strand":-1,"description":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45065]"}, {"versioned_ensembl_gene_id":"ENSG00000260264.1","gene_symbol":"LINC2194","gene_name":"long intergenic non-protein coding RNA 2194 [Source:HGNC Symbol;Acc:HGNC:53057]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371142","summary":null,"start":24236104,"end":24252863,"strand":1,"description":"long intergenic non-protein coding RNA 2194 [Source:HGNC Symbol;Acc:HGNC:53057]"}, {"versioned_ensembl_gene_id":"ENSG00000011009.10","gene_symbol":"LYPLA2","gene_name":"lysophospholipase II [Source:HGNC Symbol;Acc:HGNC:6738]","synonyms":"APT-2","biotype":"protein_coding","ncbi_id":"11313","summary":"Lysophospholipases are enzymes that act on biological membranes to regulate the multifunctional lysophospholipids. There are alternatively spliced transcript variants described for this gene but the full length nature is not known yet. [provided by RefSeq, Jul 2008]","start":23790970,"end":23795539,"strand":1,"description":"lysophospholipase II [Source:HGNC Symbol;Acc:HGNC:6738]"}, {"versioned_ensembl_gene_id":"ENSG00000122642.10","gene_symbol":"FKBP9","gene_name":"FK506 binding protein 9 [Source:HGNC Symbol;Acc:HGNC:3725]","synonyms":"FKBP63,FKBP60","biotype":"protein_coding","ncbi_id":"11328","summary":null,"start":32957404,"end":33006931,"strand":1,"description":"FK506 binding protein 9 [Source:HGNC Symbol;Acc:HGNC:3725]"}, {"versioned_ensembl_gene_id":"ENSG00000120693.13","gene_symbol":"SMAD9","gene_name":"SMAD family member 9 [Source:HGNC Symbol;Acc:HGNC:6774]","synonyms":"SMAD8/9,SMAD8,MADH9,MADH6","biotype":"protein_coding","ncbi_id":"4093","summary":"The protein encoded by this gene is a member of the SMAD family, which transduces signals from TGF-beta family members. The encoded protein is activated by bone morphogenetic proteins and interacts with SMAD4. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]","start":36844831,"end":36920765,"strand":-1,"description":"SMAD family member 9 [Source:HGNC Symbol;Acc:HGNC:6774]"}, {"versioned_ensembl_gene_id":"ENSG00000229373.8","gene_symbol":"LINC00452","gene_name":"long intergenic non-protein coding RNA 452 [Source:HGNC Symbol;Acc:HGNC:42800]","synonyms":"LINC00453","biotype":"lincRNA","ncbi_id":"643365","summary":null,"start":113888306,"end":113923512,"strand":1,"description":"long intergenic non-protein coding RNA 452 [Source:HGNC Symbol;Acc:HGNC:42800]"}, {"versioned_ensembl_gene_id":"ENSG00000228687.1","gene_symbol":"AL035407.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":192796533,"end":192797205,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224312.1","gene_symbol":"MCCD1P2","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]","synonyms":"BPG309N1.16","biotype":"unprocessed_pseudogene","ncbi_id":"100048924","summary":null,"start":29994437,"end":29995314,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33462]"}, {"versioned_ensembl_gene_id":"ENSG00000226814.2","gene_symbol":"AL035407.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":192800571,"end":192801141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281831.1","gene_symbol":"HCP5B","gene_name":"HLA complex P5B (non-protein coding) [Source:NCBI gene;Acc:352990]","synonyms":"P5.9,P5-10,HCP5P10","biotype":"lincRNA","ncbi_id":"352990","summary":null,"start":29871895,"end":29873783,"strand":-1,"description":"HLA complex P5B (non-protein coding) [Source:NCBI gene;Acc:352990]"}, {"versioned_ensembl_gene_id":"ENSG00000119866.20","gene_symbol":"BCL11A","gene_name":"B-cell CLL/lymphoma 11A [Source:HGNC Symbol;Acc:HGNC:13221]","synonyms":"ZNF856,HBFQTL5,EVI9,CTIP1,BCL11A-XL,BCL11A-S,BCL11A-L","biotype":"protein_coding","ncbi_id":"53335","summary":"This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":60451167,"end":60553567,"strand":-1,"description":"B-cell CLL/lymphoma 11A [Source:HGNC Symbol;Acc:HGNC:13221]"}, {"versioned_ensembl_gene_id":"ENSG00000066379.14","gene_symbol":"ZNRD1","gene_name":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]","synonyms":"hZR14,tctex-6,RPA12,HTEX-6","biotype":"protein_coding","ncbi_id":"30834","summary":"This gene encodes a DNA-directed RNA polymerase I subunit. The encoded protein contains two potential zinc-binding motifs and may play a role in regulation of cell proliferation. The encoded protein may be involved in cancer and human immunodeficiency virus progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":30058899,"end":30064909,"strand":1,"description":"zinc ribbon domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13182]"}, {"versioned_ensembl_gene_id":"ENSG00000278565.4","gene_symbol":"CEACAM21","gene_name":"carcinoembryonic antigen related cell adhesion molecule 21 [Source:HGNC Symbol;Acc:HGNC:28834]","synonyms":"FLJ13540,R29124_1","biotype":"protein_coding","ncbi_id":"90273","summary":null,"start":41557860,"end":41595186,"strand":1,"description":"carcinoembryonic antigen related cell adhesion molecule 21 [Source:HGNC Symbol;Acc:HGNC:28834]"}, {"versioned_ensembl_gene_id":"ENSG00000215356.4","gene_symbol":"ZNF705B","gene_name":"zinc finger protein 705B [Source:HGNC Symbol;Acc:HGNC:32284]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132396","summary":null,"start":7926337,"end":7952413,"strand":1,"description":"zinc finger protein 705B [Source:HGNC Symbol;Acc:HGNC:32284]"}, {"versioned_ensembl_gene_id":"ENSG00000230661.1","gene_symbol":"YY1P1","gene_name":"YY1 transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45094]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419963","summary":null,"start":70485336,"end":70486325,"strand":-1,"description":"YY1 transcription factor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45094]"}, {"versioned_ensembl_gene_id":"ENSG00000237505.6","gene_symbol":"PKN2-AS1","gene_name":"PKN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50597]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927891","summary":null,"start":88537513,"end":88685204,"strand":-1,"description":"PKN2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50597]"}, {"versioned_ensembl_gene_id":"ENSG00000178127.12","gene_symbol":"NDUFV2","gene_name":"NADH:ubiquinone oxidoreductase core subunit V2 [Source:HGNC Symbol;Acc:HGNC:7717]","synonyms":"CI-24k","biotype":"protein_coding","ncbi_id":"4729","summary":"The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found in one case of early onset hypertrophic cardiomyopathy and encephalopathy. A non-transcribed pseudogene of this locus is found on chromosome 19. [provided by RefSeq, Oct 2009]","start":9102630,"end":9134345,"strand":1,"description":"NADH:ubiquinone oxidoreductase core subunit V2 [Source:HGNC Symbol;Acc:HGNC:7717]"}, {"versioned_ensembl_gene_id":"ENSG00000273172.1","gene_symbol":"LINC02091","gene_name":"long intergenic non-protein coding RNA 2091 [Source:HGNC Symbol;Acc:HGNC:52942]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506371","summary":null,"start":183824,"end":191587,"strand":-1,"description":"long intergenic non-protein coding RNA 2091 [Source:HGNC Symbol;Acc:HGNC:52942]"}, {"versioned_ensembl_gene_id":"ENSG00000168952.15","gene_symbol":"STXBP6","gene_name":"syntaxin binding protein 6 [Source:HGNC Symbol;Acc:HGNC:19666]","synonyms":"HSPC156,amisyn","biotype":"protein_coding","ncbi_id":"29091","summary":"STXBP6 binds components of the SNARE complex (see MIM 603215) and may be involved in regulating SNARE complex formation (Scales et al., 2002 [PubMed 12145319]).[supplied by OMIM, Mar 2008]","start":24809656,"end":25050297,"strand":-1,"description":"syntaxin binding protein 6 [Source:HGNC Symbol;Acc:HGNC:19666]"}, {"versioned_ensembl_gene_id":"ENSG00000237959.1","gene_symbol":"RPL36AP10","gene_name":"ribosomal protein L36a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36175]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271140","summary":null,"start":88577880,"end":88578201,"strand":1,"description":"ribosomal protein L36a pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:36175]"}, {"versioned_ensembl_gene_id":"ENSG00000273633.1","gene_symbol":"CDC42EP5","gene_name":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]","synonyms":"Borg3,CEP5","biotype":"protein_coding","ncbi_id":"148170","summary":"Cell division control protein 42 (CDC42), a small Rho GTPase, regulates the formation of F-actin-containing structures through its interaction with the downstream effector proteins. The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins. Borg family proteins contain a CRIB (Cdc42/Rac interactive-binding) domain. They bind to CDC42 and regulate its function negatively. The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding. The protein may also play a role in septin organization and inducing pseudopodia formation in fibroblasts [provided by RefSeq, Jul 2013]","start":54397172,"end":54405337,"strand":-1,"description":"CDC42 effector protein 5 [Source:HGNC Symbol;Acc:HGNC:17408]"}, {"versioned_ensembl_gene_id":"ENSG00000229907.3","gene_symbol":"DEFB108A","gene_name":"defensin beta 108A [Source:HGNC Symbol;Acc:HGNC:18089]","synonyms":"DEFB108P1,DEFB108,DEFB-8","biotype":"unprocessed_pseudogene","ncbi_id":"503694","summary":null,"start":7934412,"end":7938770,"strand":-1,"description":"defensin beta 108A [Source:HGNC Symbol;Acc:HGNC:18089]"}, {"versioned_ensembl_gene_id":"ENSG00000181211.1","gene_symbol":"HECW1-IT1","gene_name":"HECW1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41465]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100127950","summary":null,"start":43117896,"end":43163187,"strand":1,"description":"HECW1 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41465]"}, {"versioned_ensembl_gene_id":"ENSG00000204983.13","gene_symbol":"PRSS1","gene_name":"protease, serine 1 [Source:HGNC Symbol;Acc:HGNC:9475]","synonyms":"TRY1","biotype":"protein_coding","ncbi_id":"5644","summary":"This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is secreted by the pancreas and cleaved to its active form in the small intestine. It is active on peptide linkages involving the carboxyl group of lysine or arginine. Mutations in this gene are associated with hereditary pancreatitis. This gene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. [provided by RefSeq, Jul 2008]","start":142749468,"end":142753076,"strand":1,"description":"protease, serine 1 [Source:HGNC Symbol;Acc:HGNC:9475]"}, {"versioned_ensembl_gene_id":"ENSG00000271163.1","gene_symbol":"AC004840.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2393847,"end":2394131,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277507.2","gene_symbol":"AP000351.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24030925,"end":24031599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228680.1","gene_symbol":"AC004692.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43239066,"end":43249268,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276005.1","gene_symbol":"AC138749.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28601112,"end":28602743,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232187.1","gene_symbol":"FTH1P7","gene_name":"ferritin heavy chain 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3994]","synonyms":"FTHL7","biotype":"processed_pseudogene","ncbi_id":"2500","summary":null,"start":22696023,"end":22696574,"strand":-1,"description":"ferritin heavy chain 1 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:3994]"}, {"versioned_ensembl_gene_id":"ENSG00000231638.1","gene_symbol":"LUARIS","gene_name":"lncRNA upregulator of antiviral response interferon signaling [Source:HGNC Symbol;Acc:HGNC:40992]","synonyms":"lncRNA#32","biotype":"antisense_RNA","ncbi_id":"100506895","summary":null,"start":43508728,"end":43522542,"strand":-1,"description":"lncRNA upregulator of antiviral response interferon signaling [Source:HGNC Symbol;Acc:HGNC:40992]"}, {"versioned_ensembl_gene_id":"ENSG00000244215.1","gene_symbol":"LINC02016","gene_name":"long intergenic non-protein coding RNA 2016 [Source:HGNC Symbol;Acc:HGNC:52851]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927123","summary":null,"start":127322307,"end":127390670,"strand":-1,"description":"long intergenic non-protein coding RNA 2016 [Source:HGNC Symbol;Acc:HGNC:52851]"}, {"versioned_ensembl_gene_id":"ENSG00000279895.1","gene_symbol":"CU633904.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7421442,"end":7425839,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282380.1","gene_symbol":"TRBJ2-4","gene_name":"T-cell receptor beta joining 2-4 [Source:HGNC Symbol;Acc:HGNC:12172]","synonyms":"TRBJ24,TCRBJ2S4","biotype":"TR_J_gene","ncbi_id":"28625","summary":null,"start":142858091,"end":142858140,"strand":1,"description":"T-cell receptor beta joining 2-4 [Source:HGNC Symbol;Acc:HGNC:12172]"}, {"versioned_ensembl_gene_id":"ENSG00000232006.8","gene_symbol":"AC005537.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42954135,"end":43113931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282820.1","gene_symbol":"TRBJ2-5","gene_name":"T-cell receptor beta joining 2-5 [Source:HGNC Symbol;Acc:HGNC:12173]","synonyms":"TRBJ25,TCRBJ2S5","biotype":"TR_J_gene","ncbi_id":"28624","summary":null,"start":142858212,"end":142858259,"strand":1,"description":"T-cell receptor beta joining 2-5 [Source:HGNC Symbol;Acc:HGNC:12173]"}, {"versioned_ensembl_gene_id":"ENSG00000133134.11","gene_symbol":"BEX2","gene_name":"brain expressed X-linked 2 [Source:HGNC Symbol;Acc:HGNC:30933]","synonyms":"DJ79P11.1","biotype":"protein_coding","ncbi_id":"84707","summary":"This gene belongs to the brain expressed X-linked gene family. The encoded protein interacts with the transcription factor LIM domain only 2 in a DNA-binding complex that recognizes the E-box element and promotes transcription. This gene has been found to be a tumor suppressor that is silenced in human glioma. In breast cancer cells, this gene product modulates apoptosis in response to estrogen and tamoxifen, and enhances the anti-proliferative effect of tamoxifen. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","start":103309346,"end":103311046,"strand":-1,"description":"brain expressed X-linked 2 [Source:HGNC Symbol;Acc:HGNC:30933]"}, {"versioned_ensembl_gene_id":"ENSG00000240562.1","gene_symbol":"AC016968.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127489553,"end":127490787,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213335.4","gene_symbol":"CLNS1AP1","gene_name":"chloride nucleotide-sensitive channel 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2081]","synonyms":"ICln,CLNS1B","biotype":"processed_pseudogene","ncbi_id":"1204","summary":null,"start":54485169,"end":54485850,"strand":-1,"description":"chloride nucleotide-sensitive channel 1A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:2081]"}, {"versioned_ensembl_gene_id":"ENSG00000239921.3","gene_symbol":"LINC01471","gene_name":"long intergenic non-protein coding RNA 1471 [Source:HGNC Symbol;Acc:HGNC:51106]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927149","summary":null,"start":127480690,"end":127537780,"strand":-1,"description":"long intergenic non-protein coding RNA 1471 [Source:HGNC Symbol;Acc:HGNC:51106]"}, {"versioned_ensembl_gene_id":"ENSG00000136213.9","gene_symbol":"CHST12","gene_name":"carbohydrate sulfotransferase 12 [Source:HGNC Symbol;Acc:HGNC:17423]","synonyms":"C4ST2,C4S-2","biotype":"protein_coding","ncbi_id":"55501","summary":"The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin and desulfated dermatan sulfate. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. Alternatively spliced transcript variants differing only in their 5' UTRs have been found for this gene. [provided by RefSeq, Aug 2011]","start":2403560,"end":2448483,"strand":1,"description":"carbohydrate sulfotransferase 12 [Source:HGNC Symbol;Acc:HGNC:17423]"}, {"versioned_ensembl_gene_id":"ENSG00000213697.3","gene_symbol":"CTBP2P6","gene_name":"C-terminal binding protein 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45198]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"120449","summary":null,"start":43522036,"end":43523264,"strand":1,"description":"C-terminal binding protein 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:45198]"}, {"versioned_ensembl_gene_id":"ENSG00000216347.1","gene_symbol":"RPL10P10","gene_name":"ribosomal protein L10 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35486]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129930","summary":null,"start":54602487,"end":54603150,"strand":-1,"description":"ribosomal protein L10 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35486]"}, {"versioned_ensembl_gene_id":"ENSG00000142627.12","gene_symbol":"EPHA2","gene_name":"EPH receptor A2 [Source:HGNC Symbol;Acc:HGNC:3386]","synonyms":"ECK","biotype":"protein_coding","ncbi_id":"1969","summary":"This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Mutations in this gene are the cause of certain genetically-related cataract disorders.[provided by RefSeq, May 2010]","start":16124337,"end":16156087,"strand":-1,"description":"EPH receptor A2 [Source:HGNC Symbol;Acc:HGNC:3386]"}, {"versioned_ensembl_gene_id":"ENSG00000282975.1","gene_symbol":"LINC02034","gene_name":"long intergenic non-protein coding RNA 2034 [Source:HGNC Symbol;Acc:HGNC:52868]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107986125","summary":null,"start":127537937,"end":127540485,"strand":1,"description":"long intergenic non-protein coding RNA 2034 [Source:HGNC Symbol;Acc:HGNC:52868]"}, {"versioned_ensembl_gene_id":"ENSG00000274084.4","gene_symbol":"LAIR2","gene_name":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]","synonyms":"CD306","biotype":"protein_coding","ncbi_id":"3904","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1, a membrane-bound receptor that modulates innate immune response. The protein encoded by this locus is a soluble receptor that may play roles in both inhibition of collagen-induced platelet aggregation and vessel formation during placental implantation. This gene maps to a region of 19q13.4, termed the leukocyte receptor cluster, which contains 29 genes in the immunoglobulin superfamily. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013]","start":54429706,"end":54442942,"strand":1,"description":"leukocyte associated immunoglobulin like receptor 2 [Source:HGNC Symbol;Acc:HGNC:6478]"}, {"versioned_ensembl_gene_id":"ENSG00000282860.1","gene_symbol":"AC084035.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":127571232,"end":127571838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231845.3","gene_symbol":"HMGB3P14","gene_name":"high mobility group box 3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39306]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873899","summary":null,"start":134170487,"end":134171085,"strand":1,"description":"high mobility group box 3 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39306]"}, {"versioned_ensembl_gene_id":"ENSG00000132361.16","gene_symbol":"CLUH","gene_name":"clustered mitochondria homolog [Source:HGNC Symbol;Acc:HGNC:29094]","synonyms":"KIAA0664,CLU1","biotype":"protein_coding","ncbi_id":"23277","summary":null,"start":2689386,"end":2712663,"strand":-1,"description":"clustered mitochondria homolog [Source:HGNC Symbol;Acc:HGNC:29094]"}, {"versioned_ensembl_gene_id":"ENSG00000100034.13","gene_symbol":"PPM1F","gene_name":"protein phosphatase, Mg2+/Mn2+ dependent 1F [Source:HGNC Symbol;Acc:HGNC:19388]","synonyms":"KIAA0015,FEM-2,CaMKPase,CAMKP,POPX2","biotype":"protein_coding","ncbi_id":"9647","summary":"The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. This phosphatase can interact with Rho guanine nucleotide exchange factors (PIX), and thus block the effects of p21-activated kinase 1 (PAK), a protein kinase mediating biological effects downstream of Rho GTPases. Calcium/calmodulin-dependent protein kinase II gamma (CAMK2G/CAMK-II) is found to be one of the substrates of this phosphatase. The overexpression of this phosphatase or CAMK2G has been shown to mediate caspase-dependent apoptosis. An alternatively spliced transcript variant has been identified, but its full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":21919420,"end":21952837,"strand":-1,"description":"protein phosphatase, Mg2+/Mn2+ dependent 1F [Source:HGNC Symbol;Acc:HGNC:19388]"}, {"versioned_ensembl_gene_id":"ENSG00000186076.5","gene_symbol":"AC012085.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":93640822,"end":93641586,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225777.1","gene_symbol":"DDX39AP1","gene_name":"DEAD-box helicase 39A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39664]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646164","summary":null,"start":22704739,"end":22706206,"strand":-1,"description":"DEAD-box helicase 39A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39664]"}, {"versioned_ensembl_gene_id":"ENSG00000234001.1","gene_symbol":"AC000111.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117586207,"end":117586416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237974.1","gene_symbol":"AC000111.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":117487737,"end":117487929,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232661.1","gene_symbol":"AC000111.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117560733,"end":117564676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130227.16","gene_symbol":"XPO7","gene_name":"exportin 7 [Source:HGNC Symbol;Acc:HGNC:14108]","synonyms":"RANBP16,KIAA0745","biotype":"protein_coding","ncbi_id":"23039","summary":"The transport of protein and large RNAs through the nuclear pore complexes (NPC) is an energy-dependent and regulated process. The import of proteins with a nuclear localization signal (NLS) is accomplished by recognition of one or more clusters of basic amino acids by the importin-alpha/beta complex; see MIM 600685 and MIM 602738. The small GTPase RAN (MIM 601179) plays a key role in NLS-dependent protein import. RAN-binding protein-16 is a member of the importin-beta superfamily of nuclear transport receptors.[supplied by OMIM, Jul 2002]","start":21919671,"end":22006585,"strand":1,"description":"exportin 7 [Source:HGNC Symbol;Acc:HGNC:14108]"}, {"versioned_ensembl_gene_id":"ENSG00000236711.2","gene_symbol":"SMAD9-IT1","gene_name":"SMAD9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39963]","synonyms":"SMAD9-AS1","biotype":"sense_intronic","ncbi_id":"100874072","summary":null,"start":36849366,"end":36850046,"strand":-1,"description":"SMAD9 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39963]"}, {"versioned_ensembl_gene_id":"ENSG00000237952.1","gene_symbol":"RPL7AP73","gene_name":"ribosomal protein L7a pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:41968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873817","summary":null,"start":22803296,"end":22803648,"strand":1,"description":"ribosomal protein L7a pseudogene 73 [Source:HGNC Symbol;Acc:HGNC:41968]"}, {"versioned_ensembl_gene_id":"ENSG00000226507.1","gene_symbol":"IPMKP1","gene_name":"inositol polyphosphate multikinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39354]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"401730","summary":null,"start":22837026,"end":22837880,"strand":-1,"description":"inositol polyphosphate multikinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39354]"}, {"versioned_ensembl_gene_id":"ENSG00000077063.10","gene_symbol":"CTTNBP2","gene_name":"cortactin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15679]","synonyms":"Orf4,KIAA1758,CORTBP2,C7orf8","biotype":"protein_coding","ncbi_id":"83992","summary":"This gene encodes a protein with six ankyrin repeats and several proline-rich regions. A similar gene in rat interacts with a central regulator of the actin cytoskeleton. [provided by RefSeq, Jul 2008]","start":117710651,"end":117874139,"strand":-1,"description":"cortactin binding protein 2 [Source:HGNC Symbol;Acc:HGNC:15679]"}, {"versioned_ensembl_gene_id":"ENSG00000231650.1","gene_symbol":"RFESDP1","gene_name":"Rieske (Fe-S) domain containing pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39420]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129167","summary":null,"start":22850101,"end":22850561,"strand":1,"description":"Rieske (Fe-S) domain containing pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39420]"}, {"versioned_ensembl_gene_id":"ENSG00000205413.7","gene_symbol":"SAMD9","gene_name":"sterile alpha motif domain containing 9 [Source:HGNC Symbol;Acc:HGNC:1348]","synonyms":"KIAA2004,FLJ20073,C7orf5","biotype":"protein_coding","ncbi_id":"54809","summary":"This gene encodes a sterile alpha motif domain-containing protein. The encoded protein localizes to the cytoplasm and may play a role in regulating cell proliferation and apoptosis. Mutations in this gene are the cause of normophosphatemic familial tumoral calcinosis. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Jul 2010]","start":93099513,"end":93118023,"strand":-1,"description":"sterile alpha motif domain containing 9 [Source:HGNC Symbol;Acc:HGNC:1348]"}, {"versioned_ensembl_gene_id":"ENSG00000006116.3","gene_symbol":"CACNG3","gene_name":"calcium voltage-gated channel auxiliary subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:1407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10368","summary":"The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family. This gene is a susceptibility locus for childhood absence epilepsy. [provided by RefSeq, Dec 2010]","start":24255553,"end":24362801,"strand":1,"description":"calcium voltage-gated channel auxiliary subunit gamma 3 [Source:HGNC Symbol;Acc:HGNC:1407]"}, {"versioned_ensembl_gene_id":"ENSG00000230535.1","gene_symbol":"BASP1P1","gene_name":"brain abundant, membrane attached signal protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39418]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646201","summary":null,"start":22897341,"end":22898005,"strand":-1,"description":"brain abundant, membrane attached signal protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39418]"}, {"versioned_ensembl_gene_id":"ENSG00000234685.1","gene_symbol":"NUS1P2","gene_name":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38473]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646208","summary":null,"start":22915651,"end":22916523,"strand":1,"description":"NUS1 dehydrodolichyl diphosphate synthase subunit pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38473]"}, {"versioned_ensembl_gene_id":"ENSG00000262619.1","gene_symbol":"LINC00621","gene_name":"long intergenic non-protein coding RNA 621 [Source:HGNC Symbol;Acc:HGNC:44227]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996930","summary":null,"start":22894656,"end":22916369,"strand":-1,"description":"long intergenic non-protein coding RNA 621 [Source:HGNC Symbol;Acc:HGNC:44227]"}, {"versioned_ensembl_gene_id":"ENSG00000230832.3","gene_symbol":"AC241584.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147082338,"end":147083578,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283342.1","gene_symbol":"AC241584.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":147099482,"end":147124285,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253349.1","gene_symbol":"COX6B1P6","gene_name":"cytochrome c oxidase subunit 6B1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37676]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462851","summary":null,"start":89823548,"end":89823802,"strand":-1,"description":"cytochrome c oxidase subunit 6B1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:37676]"}, {"versioned_ensembl_gene_id":"ENSG00000281556.2","gene_symbol":"AC243960.11","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41557862,"end":41563804,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175782.9","gene_symbol":"SLC35E3","gene_name":"solute carrier family 35 member E3 [Source:HGNC Symbol;Acc:HGNC:20864]","synonyms":"BLOV1","biotype":"protein_coding","ncbi_id":"55508","summary":null,"start":68746106,"end":68793964,"strand":1,"description":"solute carrier family 35 member E3 [Source:HGNC Symbol;Acc:HGNC:20864]"}, {"versioned_ensembl_gene_id":"ENSG00000275103.1","gene_symbol":"AF117829.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89826593,"end":89833564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182916.7","gene_symbol":"TCEAL7","gene_name":"transcription elongation factor A like 7 [Source:HGNC Symbol;Acc:HGNC:28336]","synonyms":"WEX5,MGC23947","biotype":"protein_coding","ncbi_id":"56849","summary":null,"start":103330196,"end":103332326,"strand":1,"description":"transcription elongation factor A like 7 [Source:HGNC Symbol;Acc:HGNC:28336]"}, {"versioned_ensembl_gene_id":"ENSG00000228415.3","gene_symbol":"PTMAP1","gene_name":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]","synonyms":"Em:AB023049.6","biotype":"processed_pseudogene","ncbi_id":"5758","summary":null,"start":30633632,"end":30633956,"strand":1,"description":"prothymosin, alpha pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:9624]"}, {"versioned_ensembl_gene_id":"ENSG00000228825.1","gene_symbol":"LAMTOR3P1","gene_name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39726]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130119","summary":null,"start":36922539,"end":36922908,"strand":1,"description":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39726]"}, {"versioned_ensembl_gene_id":"ENSG00000123999.4","gene_symbol":"INHA","gene_name":"inhibin alpha subunit [Source:HGNC Symbol;Acc:HGNC:6065]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3623","summary":"This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate multiple peptide products, including the alpha subunit of the inhibin A and B protein complexes. These complexes negatively regulate follicle stimulating hormone secretion from the pituitary gland. Inhibins have also been implicated in regulating numerous cellular processes including cell proliferation, apoptosis, immune response and hormone secretion. Mutations in this gene may be associated with male infertility and premature ovarian failure in female human patients. [provided by RefSeq, Aug 2016]","start":219569162,"end":219575713,"strand":1,"description":"inhibin alpha subunit [Source:HGNC Symbol;Acc:HGNC:6065]"}, {"versioned_ensembl_gene_id":"ENSG00000236202.1","gene_symbol":"GRM7-AS1","gene_name":"GRM7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40267]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873937","summary":null,"start":7519741,"end":7560333,"strand":-1,"description":"GRM7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40267]"}, {"versioned_ensembl_gene_id":"ENSG00000281224.1","gene_symbol":"AC243960.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":41559910,"end":41560616,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250344.1","gene_symbol":"AC105254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":121071429,"end":121080476,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137343.17","gene_symbol":"ATAT1","gene_name":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]","synonyms":"MEC17,C6orf134,FLJ13158,Em:AB023049.7","biotype":"protein_coding","ncbi_id":"79969","summary":"This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30626842,"end":30646823,"strand":1,"description":"alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:21186]"}, {"versioned_ensembl_gene_id":"ENSG00000241673.1","gene_symbol":"RPS27P12","gene_name":"ribosomal protein S27 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35843]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271117","summary":null,"start":129218093,"end":129218350,"strand":-1,"description":"ribosomal protein S27 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:35843]"}, {"versioned_ensembl_gene_id":"ENSG00000173376.13","gene_symbol":"NDNF","gene_name":"neuron derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:26256]","synonyms":"FLJ23191,C4orf31","biotype":"protein_coding","ncbi_id":"79625","summary":null,"start":121035613,"end":121073021,"strand":-1,"description":"neuron derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:26256]"}, {"versioned_ensembl_gene_id":"ENSG00000196277.15","gene_symbol":"GRM7","gene_name":"glutamate metabotropic receptor 7 [Source:HGNC Symbol;Acc:HGNC:4599]","synonyms":"PPP1R87,MGLUR7,mGlu7,GPRC1G,GLUR7","biotype":"protein_coding","ncbi_id":"2917","summary":"L-glutamate is the major excitatory neurotransmitter in the central nervous system, and it activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors that have been divided into three groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I includes GRM1 and GRM5, and these receptors have been shown to activate phospholipase C. Group II includes GRM2 and GRM3, while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]","start":6770001,"end":7741533,"strand":1,"description":"glutamate metabotropic receptor 7 [Source:HGNC Symbol;Acc:HGNC:4599]"}, {"versioned_ensembl_gene_id":"ENSG00000269068.1","gene_symbol":"AC009955.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":219559083,"end":219559626,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124006.14","gene_symbol":"OBSL1","gene_name":"obscurin like 1 [Source:HGNC Symbol;Acc:HGNC:29092]","synonyms":"KIAA0657","biotype":"protein_coding","ncbi_id":"23363","summary":"Cytoskeletal adaptor proteins function in linking the internal cytoskeleton of cells to the cell membrane. This gene encodes a cytoskeletal adaptor protein, which is a member of the Unc-89/obscurin family. The protein contains multiple N- and C-terminal immunoglobulin (Ig)-like domains and a central fibronectin type 3 domain. Mutations in this gene cause 3M syndrome type 2. Alternatively spliced transcript variants encoding different isoforms have been found in this gene. [provided by RefSeq, Mar 2010]","start":219550729,"end":219571859,"strand":-1,"description":"obscurin like 1 [Source:HGNC Symbol;Acc:HGNC:29092]"}, {"versioned_ensembl_gene_id":"ENSG00000013288.8","gene_symbol":"MAN2B2","gene_name":"mannosidase alpha class 2B member 2 [Source:HGNC Symbol;Acc:HGNC:29623]","synonyms":"KIAA0935","biotype":"protein_coding","ncbi_id":"23324","summary":null,"start":6575175,"end":6623362,"strand":1,"description":"mannosidase alpha class 2B member 2 [Source:HGNC Symbol;Acc:HGNC:29623]"}, {"versioned_ensembl_gene_id":"ENSG00000116741.7","gene_symbol":"RGS2","gene_name":"regulator of G protein signaling 2 [Source:HGNC Symbol;Acc:HGNC:9998]","synonyms":"G0S8","biotype":"protein_coding","ncbi_id":"5997","summary":"Regulator of G protein signaling (RGS) family members are regulatory molecules that act as GTPase activating proteins (GAPs) for G alpha subunits of heterotrimeric G proteins. RGS proteins are able to deactivate G protein subunits of the Gi alpha, Go alpha and Gq alpha subtypes. They drive G proteins into their inactive GDP-bound forms. Regulator of G protein signaling 2 belongs to this family. The protein acts as a mediator of myeloid differentiation and may play a role in leukemogenesis. [provided by RefSeq, Aug 2009]","start":192809039,"end":192812283,"strand":1,"description":"regulator of G protein signaling 2 [Source:HGNC Symbol;Acc:HGNC:9998]"}, {"versioned_ensembl_gene_id":"ENSG00000235321.1","gene_symbol":"AC007556.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":169100743,"end":169101210,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106615.9","gene_symbol":"RHEB","gene_name":"Ras homolog enriched in brain [Source:HGNC Symbol;Acc:HGNC:10011]","synonyms":"RHEB2","biotype":"protein_coding","ncbi_id":"6009","summary":"This gene is a member of the small GTPase superfamily and encodes a lipid-anchored, cell membrane protein with five repeats of the RAS-related GTP-binding region. This protein is vital in regulation of growth and cell cycle progression due to its role in the insulin/TOR/S6K signaling pathway. The protein has GTPase activity and shuttles between a GDP-bound form and a GTP-bound form, and farnesylation of the protein is required for this activity. Three pseudogenes have been mapped, two on chromosome 10 and one on chromosome 22. [provided by RefSeq, Jul 2008]","start":151466012,"end":151520120,"strand":-1,"description":"Ras homolog enriched in brain [Source:HGNC Symbol;Acc:HGNC:10011]"}, {"versioned_ensembl_gene_id":"ENSG00000262198.1","gene_symbol":"AL157931.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22918591,"end":22924602,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283075.1","gene_symbol":"AL157931.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22931537,"end":22931999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166886.12","gene_symbol":"NAB2","gene_name":"NGFI-A binding protein 2 [Source:HGNC Symbol;Acc:HGNC:7627]","synonyms":"MADER","biotype":"protein_coding","ncbi_id":"4665","summary":"This gene encodes a member of the family of NGFI-A binding (NAB) proteins, which function in the nucleus to repress transcription induced by some members of the EGR (early growth response) family of transactivators. NAB proteins can homo- or hetero-multimerize with other EGR or NAB proteins through a conserved N-terminal domain, and repress transcription through two partially redundant C-terminal domains. Transcriptional repression by the encoded protein is mediated in part by interactions with the nucleosome remodeling and deactylase (NuRD) complex. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":57088894,"end":57095476,"strand":1,"description":"NGFI-A binding protein 2 [Source:HGNC Symbol;Acc:HGNC:7627]"}, {"versioned_ensembl_gene_id":"ENSG00000280590.1","gene_symbol":"AF250324.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189703881,"end":189704490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233440.2","gene_symbol":"HMGA1P6","gene_name":"high mobility group AT-hook 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19121]","synonyms":"HMGA1L6","biotype":"processed_pseudogene","ncbi_id":"100130029","summary":null,"start":23134174,"end":23134564,"strand":1,"description":"high mobility group AT-hook 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:19121]"}, {"versioned_ensembl_gene_id":"ENSG00000263847.1","gene_symbol":"AP005899.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9112404,"end":9115877,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281015.1","gene_symbol":"LINC01596","gene_name":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]","synonyms":"TCONS_00007705","biotype":"lincRNA","ncbi_id":"105377617","summary":null,"start":189885470,"end":189888818,"strand":1,"description":"long intergenic non-protein coding RNA 1596 [Source:NCBI gene;Acc:105377617]"}, {"versioned_ensembl_gene_id":"ENSG00000229483.2","gene_symbol":"LINC00362","gene_name":"long intergenic non-protein coding RNA 362 [Source:HGNC Symbol;Acc:HGNC:42682]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874144","summary":null,"start":23169835,"end":23170597,"strand":-1,"description":"long intergenic non-protein coding RNA 362 [Source:HGNC Symbol;Acc:HGNC:42682]"}, {"versioned_ensembl_gene_id":"ENSG00000265257.5","gene_symbol":"AP005263.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":9102736,"end":9254346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281543.2","gene_symbol":"AC226374.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189780336,"end":189944248,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244754.8","gene_symbol":"N4BP2L2","gene_name":"NEDD4 binding protein 2 like 2 [Source:HGNC Symbol;Acc:HGNC:26916]","synonyms":"PFAAP5,CG005","biotype":"protein_coding","ncbi_id":"10443","summary":null,"start":32432417,"end":32538885,"strand":-1,"description":"NEDD4 binding protein 2 like 2 [Source:HGNC Symbol;Acc:HGNC:26916]"}, {"versioned_ensembl_gene_id":"ENSG00000238049.2","gene_symbol":"Z92846.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103347462,"end":103347729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158113.12","gene_symbol":"LRRC43","gene_name":"leucine rich repeat containing 43 [Source:HGNC Symbol;Acc:HGNC:28562]","synonyms":"MGC35140","biotype":"protein_coding","ncbi_id":"254050","summary":null,"start":122167738,"end":122203471,"strand":1,"description":"leucine rich repeat containing 43 [Source:HGNC Symbol;Acc:HGNC:28562]"}, {"versioned_ensembl_gene_id":"ENSG00000266053.2","gene_symbol":"NDUFV2-AS1","gene_name":"NDUFV2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50826]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101927275","summary":null,"start":9121265,"end":9136645,"strand":-1,"description":"NDUFV2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50826]"}, {"versioned_ensembl_gene_id":"ENSG00000227959.1","gene_symbol":"AL451042.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16155211,"end":16157329,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275175.1","gene_symbol":"AC106028.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":92819598,"end":92819992,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233953.1","gene_symbol":"AC009970.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60495686,"end":60499964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273284.1","gene_symbol":"AP001033.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9259388,"end":9260390,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249213.1","gene_symbol":"AC079097.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26254883,"end":26256628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230476.1","gene_symbol":"OFD1P9Y","gene_name":"OFD1 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:23881]","synonyms":"OFDYP9,OFD1PY9,OFD1P9","biotype":"unprocessed_pseudogene","ncbi_id":"386693","summary":null,"start":22580989,"end":22614081,"strand":-1,"description":"OFD1 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:23881]"}, {"versioned_ensembl_gene_id":"ENSG00000224086.5","gene_symbol":"AC245452.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21938293,"end":21977632,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250591.3","gene_symbol":"PRSS3P1","gene_name":"protease, serine 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43787]","synonyms":"TRY5","biotype":"unprocessed_pseudogene","ncbi_id":"168330","summary":null,"start":142760415,"end":142763943,"strand":1,"description":"protease, serine 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43787]"}, {"versioned_ensembl_gene_id":"ENSG00000177993.3","gene_symbol":"ZNRF3-AS1","gene_name":"ZNRF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41927]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874123","summary":null,"start":29024999,"end":29031476,"strand":-1,"description":"ZNRF3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41927]"}, {"versioned_ensembl_gene_id":"ENSG00000275896.5","gene_symbol":"PRSS2","gene_name":"protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:9483]","synonyms":"TRY2","biotype":"protein_coding","ncbi_id":"5645","summary":"This gene belongs to the trypsin family of serine proteases and encodes anionic trypsinogen. It is part of a cluster of trypsinogen genes that are located within the T cell receptor beta locus. Enzymes of this family cleave peptide bonds that follow lysine or arginine residues. This protein is found at high levels in pancreatic juice and its upregulation is a characteristic feature of pancreatitis. This protein has also been found to activate pro-urokinase in ovarian tumors, suggesting a function in tumor invasion. In addition, this enzyme is able to cleave across the type II collagen triple helix in rheumatoid arthritis synovitis tissue, potentially participating in the degradation of type II collagen-rich cartilage matrix. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2015]","start":142760398,"end":142774564,"strand":1,"description":"protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:9483]"}, {"versioned_ensembl_gene_id":"ENSG00000235786.1","gene_symbol":"ZNRF3-IT1","gene_name":"ZNRF3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41440]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874339","summary":null,"start":28992721,"end":29018620,"strand":1,"description":"ZNRF3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41440]"}, {"versioned_ensembl_gene_id":"ENSG00000183579.15","gene_symbol":"ZNRF3","gene_name":"zinc and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:18126]","synonyms":"RNF203,KIAA1133,FLJ22057,BK747E2.3","biotype":"protein_coding","ncbi_id":"84133","summary":null,"start":28883592,"end":29057487,"strand":1,"description":"zinc and ring finger 3 [Source:HGNC Symbol;Acc:HGNC:18126]"}, {"versioned_ensembl_gene_id":"ENSG00000273589.1","gene_symbol":"AC008175.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22646031,"end":22646327,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188525.3","gene_symbol":"AC010969.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10003158,"end":10006030,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120832.9","gene_symbol":"MTERF2","gene_name":"mitochondrial transcription termination factor 2 [Source:HGNC Symbol;Acc:HGNC:30779]","synonyms":"FLJ14062,MTERFD3","biotype":"protein_coding","ncbi_id":"80298","summary":null,"start":106977291,"end":106987166,"strand":-1,"description":"mitochondrial transcription termination factor 2 [Source:HGNC Symbol;Acc:HGNC:30779]"}, {"versioned_ensembl_gene_id":"ENSG00000229007.1","gene_symbol":"EXOSC3P1","gene_name":"exosome component 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33989]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100151640","summary":null,"start":32496812,"end":32497311,"strand":1,"description":"exosome component 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33989]"}, {"versioned_ensembl_gene_id":"ENSG00000260476.1","gene_symbol":"AC104794.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10021578,"end":10022825,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000077942.18","gene_symbol":"FBLN1","gene_name":"fibulin 1 [Source:HGNC Symbol;Acc:HGNC:3600]","synonyms":"FBLN","biotype":"protein_coding","ncbi_id":"2192","summary":"Fibulin 1 is a secreted glycoprotein that becomes incorporated into a fibrillar extracellular matrix. Calcium-binding is apparently required to mediate its binding to laminin and nidogen. It mediates platelet adhesion via binding fibrinogen. Four splice variants which differ in the 3' end have been identified. Each variant encodes a different isoform, but no functional distinctions have been identified among the four variants. [provided by RefSeq, Jul 2008]","start":45502238,"end":45601135,"strand":1,"description":"fibulin 1 [Source:HGNC Symbol;Acc:HGNC:3600]"}, {"versioned_ensembl_gene_id":"ENSG00000260077.1","gene_symbol":"AC104794.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10039092,"end":10040663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166979.12","gene_symbol":"EVA1C","gene_name":"eva-1 homolog C [Source:HGNC Symbol;Acc:HGNC:13239]","synonyms":"B19,B18,PRED34,FAM176C,C21orf64,C21orf63","biotype":"protein_coding","ncbi_id":"59271","summary":null,"start":32412006,"end":32515397,"strand":1,"description":"eva-1 homolog C [Source:HGNC Symbol;Acc:HGNC:13239]"}, {"versioned_ensembl_gene_id":"ENSG00000224657.9","gene_symbol":"RBMY2BP","gene_name":"RNA binding motif protein, Y-linked, family 2, member B pseudogene [Source:HGNC Symbol;Acc:HGNC:9918]","synonyms":"RBMY2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"375850","summary":null,"start":22649245,"end":22658878,"strand":1,"description":"RNA binding motif protein, Y-linked, family 2, member B pseudogene [Source:HGNC Symbol;Acc:HGNC:9918]"}, {"versioned_ensembl_gene_id":"ENSG00000236601.2","gene_symbol":"AL732372.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":358857,"end":366052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239784.1","gene_symbol":"RPL23AP1","gene_name":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"6148","summary":null,"start":29724118,"end":29724588,"strand":-1,"description":"ribosomal protein L23a pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10318]"}, {"versioned_ensembl_gene_id":"ENSG00000206508.9","gene_symbol":"HLA-F-AS1","gene_name":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"285830","summary":null,"start":29724050,"end":29746500,"strand":-1,"description":"HLA-F antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26645]"}, {"versioned_ensembl_gene_id":"ENSG00000284733.1","gene_symbol":"OR4F29","gene_name":"olfactory receptor family 4 subfamily F member 29 [Source:HGNC Symbol;Acc:HGNC:31275]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729759","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":450703,"end":451697,"strand":-1,"description":"olfactory receptor family 4 subfamily F member 29 [Source:HGNC Symbol;Acc:HGNC:31275]"}, {"versioned_ensembl_gene_id":"ENSG00000224917.1","gene_symbol":"AC016694.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22670616,"end":22672859,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164181.13","gene_symbol":"ELOVL7","gene_name":"ELOVL fatty acid elongase 7 [Source:HGNC Symbol;Acc:HGNC:26292]","synonyms":"FLJ23563","biotype":"protein_coding","ncbi_id":"79993","summary":null,"start":60751791,"end":60844389,"strand":-1,"description":"ELOVL fatty acid elongase 7 [Source:HGNC Symbol;Acc:HGNC:26292]"}, {"versioned_ensembl_gene_id":"ENSG00000233653.3","gene_symbol":"CICP7","gene_name":"capicua transcriptional repressor pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37756]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288667","summary":null,"start":487101,"end":489906,"strand":1,"description":"capicua transcriptional repressor pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:37756]"}, {"versioned_ensembl_gene_id":"ENSG00000228463.10","gene_symbol":"AP006222.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":257864,"end":359681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224921.1","gene_symbol":"AL844851.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29720428,"end":29721418,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236619.1","gene_symbol":"AL844851.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29745740,"end":29745964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235290.1","gene_symbol":"HLA-W","gene_name":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]","synonyms":"HLA-80","biotype":"unprocessed_pseudogene","ncbi_id":"352966","summary":null,"start":29956596,"end":29958570,"strand":1,"description":"major histocompatibility complex, class I, W (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23425]"}, {"versioned_ensembl_gene_id":"ENSG00000204622.11","gene_symbol":"HLA-J","gene_name":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]","synonyms":"D6S203,HLA-CDA12,CDA12,HLA-59","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3137","summary":"This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010]","start":30005971,"end":30009956,"strand":1,"description":"major histocompatibility complex, class I, J (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4967]"}, {"versioned_ensembl_gene_id":"ENSG00000235483.1","gene_symbol":"GYG2-AS1","gene_name":"GYG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40270]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873938","summary":null,"start":2852740,"end":2853760,"strand":-1,"description":"GYG2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40270]"}, {"versioned_ensembl_gene_id":"ENSG00000269732.1","gene_symbol":"WBP1LP7","gene_name":"WW domain binding protein 1-like pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43955]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479030","summary":null,"start":439870,"end":440232,"strand":1,"description":"WW domain binding protein 1-like pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:43955]"}, {"versioned_ensembl_gene_id":"ENSG00000206509.13","gene_symbol":"HLA-F","gene_name":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3134","summary":"This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008]","start":29720222,"end":29735978,"strand":1,"description":"major histocompatibility complex, class I, F [Source:HGNC Symbol;Acc:HGNC:4963]"}, {"versioned_ensembl_gene_id":"ENSG00000151135.9","gene_symbol":"TMEM263","gene_name":"transmembrane protein 263 [Source:HGNC Symbol;Acc:HGNC:28281]","synonyms":"MGC17943,C12orf23","biotype":"protein_coding","ncbi_id":"90488","summary":null,"start":106955719,"end":106978778,"strand":1,"description":"transmembrane protein 263 [Source:HGNC Symbol;Acc:HGNC:28281]"}, {"versioned_ensembl_gene_id":"ENSG00000237094.12","gene_symbol":"AL732372.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":365389,"end":522928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000056998.19","gene_symbol":"GYG2","gene_name":"glycogenin 2 [Source:HGNC Symbol;Acc:HGNC:4700]","synonyms":"GN-2","biotype":"protein_coding","ncbi_id":"8908","summary":"This gene encodes a member of the the glycogenin family. Glycogenin is a self-glucosylating protein involved in the initiation reactions of glycogen biosynthesis. A gene on chromosome 3 encodes the muscle glycogenin and this X-linked gene encodes the glycogenin mainly present in liver; both are involved in blood glucose homeostasis. This gene has a short version on chromosome Y, which is 3' truncated and can not make a functional protein. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010]","start":2828788,"end":2882820,"strand":1,"description":"glycogenin 2 [Source:HGNC Symbol;Acc:HGNC:4700]"}, {"versioned_ensembl_gene_id":"ENSG00000225431.1","gene_symbol":"LINC01671","gene_name":"long intergenic non-protein coding RNA 1671 [Source:HGNC Symbol;Acc:HGNC:52459]","synonyms":"BC041455","biotype":"lincRNA","ncbi_id":"101928233","summary":null,"start":42599280,"end":42615058,"strand":-1,"description":"long intergenic non-protein coding RNA 1671 [Source:HGNC Symbol;Acc:HGNC:52459]"}, {"versioned_ensembl_gene_id":"ENSG00000204671.1","gene_symbol":"IL31","gene_name":"interleukin 31 [Source:HGNC Symbol;Acc:HGNC:19372]","synonyms":"IL-31","biotype":"protein_coding","ncbi_id":"386653","summary":"IL31, which is made principally by activated Th2-type T cells, interacts with a heterodimeric receptor consisting of IL31RA (MIM 609510) and OSMR (MIM 601743) that is constitutively expressed on epithelial cells and keratinocytes. IL31 may be involved in the promotion of allergic skin disorders and in regulating other allergic diseases, such as asthma (Dillon et al., 2004 [PubMed 15184896]).[supplied by OMIM, Mar 2008]","start":122172030,"end":122174199,"strand":-1,"description":"interleukin 31 [Source:HGNC Symbol;Acc:HGNC:19372]"}, {"versioned_ensembl_gene_id":"ENSG00000223639.6","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31721342,"end":31730525,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000235023.1","gene_symbol":"AP001626.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42648271,"end":42651244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250345.2","gene_symbol":"AC104090.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143760399,"end":143762093,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180644.7","gene_symbol":"PRF1","gene_name":"perforin 1 [Source:HGNC Symbol;Acc:HGNC:9360]","synonyms":"PFP,P1,HPLH2","biotype":"protein_coding","ncbi_id":"5551","summary":"This gene encodes a protein with structural similarities to complement component C9 that is important in immunity. This protein forms membrane pores that allow the release of granzymes and subsequent cytolysis of target cells. Whether pore formation occurs in the plasma membrane of target cells or in an endosomal membrane inside target cells is subject to debate. Mutations in this gene are associated with a variety of human disease including diabetes, multiple sclerosis, lymphomas, autoimmune lymphoproliferative syndrome (ALPS), aplastic anemia, and familial hemophagocytic lymphohistiocytosis type 2 (FHL2), a rare and lethal autosomal recessive disorder of early childhood. [provided by RefSeq, Aug 2017]","start":70597348,"end":70602775,"strand":-1,"description":"perforin 1 [Source:HGNC Symbol;Acc:HGNC:9360]"}, {"versioned_ensembl_gene_id":"ENSG00000250504.2","gene_symbol":"KRT18P51","gene_name":"keratin 18 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:33421]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391703","summary":null,"start":144572238,"end":144572983,"strand":1,"description":"keratin 18 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:33421]"}, {"versioned_ensembl_gene_id":"ENSG00000240132.1","gene_symbol":"AC005996.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":151501878,"end":151503463,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233265.1","gene_symbol":"MICF","gene_name":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"352957","summary":null,"start":29852363,"end":29852491,"strand":-1,"description":"MHC class I polypeptide-related sequence F (pseudogene) [Source:HGNC Symbol;Acc:HGNC:16801]"}, {"versioned_ensembl_gene_id":"ENSG00000235963.1","gene_symbol":"MCCD1P1","gene_name":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]","synonyms":"OTTHUMG00000130506","biotype":"unprocessed_pseudogene","ncbi_id":"100048903","summary":null,"start":29907783,"end":29908645,"strand":-1,"description":"mitochondrial coiled-coil domain 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33449]"}, {"versioned_ensembl_gene_id":"ENSG00000238024.1","gene_symbol":"DDX39BP2","gene_name":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]","synonyms":"BAT1P2,BPG309N1.15","biotype":"unprocessed_pseudogene","ncbi_id":"100048923","summary":null,"start":29993209,"end":29993605,"strand":1,"description":"DEAD-box helicase 39B pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:33461]"}, {"versioned_ensembl_gene_id":"ENSG00000233677.1","gene_symbol":"DDX39BP1","gene_name":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]","synonyms":"BAT1P1","biotype":"unprocessed_pseudogene","ncbi_id":"100048904","summary":null,"start":29906543,"end":29906909,"strand":1,"description":"DEAD-box helicase 39B pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33450]"}, {"versioned_ensembl_gene_id":"ENSG00000237669.1","gene_symbol":"AL671277.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30006121,"end":30007116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243661.1","gene_symbol":"WBP1LP1","gene_name":"WW domain binding protein 1-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43948]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479029","summary":null,"start":142778642,"end":142779537,"strand":-1,"description":"WW domain binding protein 1-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43948]"}, {"versioned_ensembl_gene_id":"ENSG00000120913.23","gene_symbol":"PDLIM2","gene_name":"PDZ and LIM domain 2 [Source:HGNC Symbol;Acc:HGNC:13992]","synonyms":null,"biotype":"protein_coding","ncbi_id":"64236","summary":"This gene encodes a member of the ALP subfamily of PDZ-LIM domain proteins. The encoded protein suppresses anchorage-dependent growth and promotes cell migration and adhesion through interactions with the actin cytoskeleton via the PDZ domain. The encoded protein is also a putative tumor suppressor protein, and decreased expression of this gene is associated with several malignancies including breast cancer and adult T-cell leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]","start":22578279,"end":22598025,"strand":1,"description":"PDZ and LIM domain 2 [Source:HGNC Symbol;Acc:HGNC:13992]"}, {"versioned_ensembl_gene_id":"ENSG00000204625.10","gene_symbol":"HCG9","gene_name":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]","synonyms":"HCGIX,HCGIX4,HCGIX-4,PERB11","biotype":"lincRNA","ncbi_id":"10255","summary":"This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]","start":29975112,"end":29978410,"strand":1,"description":"HLA complex group 9 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:21243]"}, {"versioned_ensembl_gene_id":"ENSG00000282431.1","gene_symbol":"AC245427.8","gene_name":null,"synonyms":null,"biotype":"TR_D_gene","ncbi_id":null,"summary":null,"start":142786213,"end":142786224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125656.8","gene_symbol":"CLPP","gene_name":"caseinolytic mitochondrial matrix peptidase proteolytic subunit [Source:HGNC Symbol;Acc:HGNC:2084]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8192","summary":"The protein encoded by this gene belongs to the peptidase family S14 and hydrolyzes proteins into small peptides in the presence of ATP and magnesium. The protein is transported into mitochondrial matrix and is associated with the inner mitochondrial membrane. [provided by RefSeq, Jul 2008]","start":6361452,"end":6368908,"strand":1,"description":"caseinolytic mitochondrial matrix peptidase proteolytic subunit [Source:HGNC Symbol;Acc:HGNC:2084]"}, {"versioned_ensembl_gene_id":"ENSG00000232757.1","gene_symbol":"ETF1P1","gene_name":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]","synonyms":"HCGVII,SUP45L2","biotype":"processed_pseudogene","ncbi_id":"6824","summary":null,"start":30031713,"end":30033003,"strand":1,"description":"eukaryotic translation termination factor 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:3478]"}, {"versioned_ensembl_gene_id":"ENSG00000165685.8","gene_symbol":"TMEM52B","gene_name":"transmembrane protein 52B [Source:HGNC Symbol;Acc:HGNC:26438]","synonyms":"FLJ31166,C12orf59","biotype":"protein_coding","ncbi_id":"120939","summary":null,"start":10170542,"end":10191801,"strand":1,"description":"transmembrane protein 52B [Source:HGNC Symbol;Acc:HGNC:26438]"}, {"versioned_ensembl_gene_id":"ENSG00000166888.11","gene_symbol":"STAT6","gene_name":"signal transducer and activator of transcription 6 [Source:HGNC Symbol;Acc:HGNC:11368]","synonyms":"IL-4-STAT,D12S1644","biotype":"protein_coding","ncbi_id":"6778","summary":"The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein plays a central role in exerting IL4 mediated biological responses. It is found to induce the expression of BCL2L1/BCL-X(L), which is responsible for the anti-apoptotic activity of IL4. Knockout studies in mice suggested the roles of this gene in differentiation of T helper 2 (Th2) cells, expression of cell surface markers, and class switch of immunoglobulins. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]","start":57095408,"end":57132139,"strand":-1,"description":"signal transducer and activator of transcription 6 [Source:HGNC Symbol;Acc:HGNC:11368]"}, {"versioned_ensembl_gene_id":"ENSG00000228078.1","gene_symbol":"HLA-U","gene_name":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]","synonyms":"Em:AB023056.13,HLA-21","biotype":"unprocessed_pseudogene","ncbi_id":"352965","summary":null,"start":29934101,"end":29934286,"strand":1,"description":"major histocompatibility complex, class I, U (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23477]"}, {"versioned_ensembl_gene_id":"ENSG00000206503.12","gene_symbol":"HLA-A","gene_name":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3105","summary":"HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020]","start":29941260,"end":29945884,"strand":1,"description":"major histocompatibility complex, class I, A [Source:HGNC Symbol;Acc:HGNC:4931]"}, {"versioned_ensembl_gene_id":"ENSG00000177225.16","gene_symbol":"GATD1","gene_name":"glutamine amidotransferase like class 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26616]","synonyms":"PDDC1,FLJ34283","biotype":"protein_coding","ncbi_id":"347862","summary":null,"start":767220,"end":777488,"strand":-1,"description":"glutamine amidotransferase like class 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26616]"}, {"versioned_ensembl_gene_id":"ENSG00000236503.1","gene_symbol":"AC009784.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136262558,"end":136263017,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232053.6","gene_symbol":"AC078845.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":136092925,"end":136437426,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258098.1","gene_symbol":"LINC02286","gene_name":"long intergenic non-protein coding RNA 2286 [Source:HGNC Symbol;Acc:HGNC:53203]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370414","summary":null,"start":25124487,"end":25126998,"strand":-1,"description":"long intergenic non-protein coding RNA 2286 [Source:HGNC Symbol;Acc:HGNC:53203]"}, {"versioned_ensembl_gene_id":"ENSG00000234871.1","gene_symbol":"LINC01032","gene_name":"long intergenic non-protein coding RNA 1032 [Source:HGNC Symbol;Acc:HGNC:49018]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724954","summary":null,"start":192937300,"end":192948257,"strand":-1,"description":"long intergenic non-protein coding RNA 1032 [Source:HGNC Symbol;Acc:HGNC:49018]"}, {"versioned_ensembl_gene_id":"ENSG00000257179.1","gene_symbol":"HMGN2P6","gene_name":"high mobility group nucleosomal binding domain 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33574]","synonyms":"HMGN2L6","biotype":"processed_pseudogene","ncbi_id":"643872","summary":null,"start":25267064,"end":25267336,"strand":-1,"description":"high mobility group nucleosomal binding domain 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:33574]"}, {"versioned_ensembl_gene_id":"ENSG00000234473.1","gene_symbol":"ZNF101P2","gene_name":"zinc finger protein 101 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44942]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"730190","summary":null,"start":192993449,"end":192994677,"strand":-1,"description":"zinc finger protein 101 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44942]"}, {"versioned_ensembl_gene_id":"ENSG00000182566.13","gene_symbol":"CLEC4G","gene_name":"C-type lectin domain family 4 member G [Source:HGNC Symbol;Acc:HGNC:24591]","synonyms":"UNQ431,LSECtin","biotype":"protein_coding","ncbi_id":"339390","summary":"This gene encodes a glycan-binding receptor and member of the C-type lectin family which plays a role in the immune response. C-type lectin receptors are pattern recognition receptors located on immune cells that play a role in the recognition and uptake of both self and non-self glycoproteins as well as mediating cell adhesion, glycoprotein clearance, and cell signaling functions. This gene's protein binds complex-type N-glycans of the viral envelope proteins of Ebola virus, West Nile filovirus, and SARS coronavirus, but not HIV or hepatitis C virus. In mouse, this protein has been shown to recognize activated T-cells and to negatively regulate T-cell receptor-mediated signalling. It also acts as a novel, liver-specific regulator of NK cell-mediated immunity in mouse. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2020]","start":7728957,"end":7733906,"strand":-1,"description":"C-type lectin domain family 4 member G [Source:HGNC Symbol;Acc:HGNC:24591]"}, {"versioned_ensembl_gene_id":"ENSG00000259040.5","gene_symbol":"BLOC1S5-TXNDC5","gene_name":"BLOC1S5-TXNDC5 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:42001]","synonyms":"MUTED-TXNDC5","biotype":"protein_coding","ncbi_id":"100526836","summary":"This locus represents naturally occurring read-through transcription between the neighboring MUTED (muted homolog) and TXNDC5 (thioredoxin domain containing 5) genes on chromosome 6. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD) and is unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":7881522,"end":8064364,"strand":-1,"description":"BLOC1S5-TXNDC5 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:42001]"}, {"versioned_ensembl_gene_id":"ENSG00000258275.1","gene_symbol":"OR7K1P","gene_name":"olfactory receptor family 7 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15366]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"81114","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":25357764,"end":25358689,"strand":1,"description":"olfactory receptor family 7 subfamily K member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:15366]"}, {"versioned_ensembl_gene_id":"ENSG00000101945.16","gene_symbol":"SUV39H1","gene_name":"suppressor of variegation 3-9 homolog 1 [Source:HGNC Symbol;Acc:HGNC:11479]","synonyms":"SUV39H,KMT1A","biotype":"protein_coding","ncbi_id":"6839","summary":"This gene encodes an evolutionarily-conserved protein containing an N-terminal chromodomain and a C-terminal SET domain. The encoded protein is a histone methyltransferase that trimethylates lysine 9 of histone H3, which results in transcriptional gene silencing. Loss of function of this gene disrupts heterochromatin formation and may cause chromosome instability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":48695554,"end":48709012,"strand":1,"description":"suppressor of variegation 3-9 homolog 1 [Source:HGNC Symbol;Acc:HGNC:11479]"}, {"versioned_ensembl_gene_id":"ENSG00000129474.15","gene_symbol":"AJUBA","gene_name":"ajuba LIM protein [Source:HGNC Symbol;Acc:HGNC:20250]","synonyms":"MGC15563,JUB","biotype":"protein_coding","ncbi_id":"84962","summary":null,"start":22971174,"end":22982642,"strand":-1,"description":"ajuba LIM protein [Source:HGNC Symbol;Acc:HGNC:20250]"}, {"versioned_ensembl_gene_id":"ENSG00000250575.1","gene_symbol":"AL732372.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":491225,"end":493241,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236679.2","gene_symbol":"RPL23AP24","gene_name":"ribosomal protein L23a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728517","summary":null,"start":347982,"end":348366,"strand":-1,"description":"ribosomal protein L23a pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:36176]"}, {"versioned_ensembl_gene_id":"ENSG00000147457.13","gene_symbol":"CHMP7","gene_name":"charged multivesicular body protein 7 [Source:HGNC Symbol;Acc:HGNC:28439]","synonyms":"MGC29816","biotype":"protein_coding","ncbi_id":"91782","summary":null,"start":23243637,"end":23262000,"strand":1,"description":"charged multivesicular body protein 7 [Source:HGNC Symbol;Acc:HGNC:28439]"}, {"versioned_ensembl_gene_id":"ENSG00000182983.14","gene_symbol":"ZNF662","gene_name":"zinc finger protein 662 [Source:HGNC Symbol;Acc:HGNC:31930]","synonyms":"FLJ45880","biotype":"protein_coding","ncbi_id":"389114","summary":null,"start":42905731,"end":42917641,"strand":1,"description":"zinc finger protein 662 [Source:HGNC Symbol;Acc:HGNC:31930]"}, {"versioned_ensembl_gene_id":"ENSG00000173213.9","gene_symbol":"TUBB8P12","gene_name":"tubulin beta 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24983]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"260334","summary":null,"start":47390,"end":49557,"strand":-1,"description":"tubulin beta 8 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:24983]"}, {"versioned_ensembl_gene_id":"ENSG00000265818.1","gene_symbol":"EEF1E1-BLOC1S5","gene_name":"EEF1E1-BLOC1S5 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49187]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100526837","summary":"This locus represents naturally occurring read-through transcription between the neighboring EEF1E1 (eukaryotic translation elongation factor 1 epsilon 1) and MUTED (muted homolog) genes on chromosome 6. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD) and is unlikely to produce a protein product. [provided by RefSeq, Dec 2010]","start":8015726,"end":8102530,"strand":-1,"description":"EEF1E1-BLOC1S5 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49187]"}, {"versioned_ensembl_gene_id":"ENSG00000269802.1","gene_symbol":"AC011491.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6343761,"end":6362149,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229915.1","gene_symbol":"AC016999.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":238427077,"end":238427729,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188428.19","gene_symbol":"BLOC1S5","gene_name":"biogenesis of lysosomal organelles complex 1 subunit 5 [Source:HGNC Symbol;Acc:HGNC:18561]","synonyms":"dJ303A1.3,MUTED,MU","biotype":"protein_coding","ncbi_id":"63915","summary":"This gene encodes a component of BLOC-1 (biogenesis of lysosome-related organelles complex 1). Components of this complex are involved in the biogenesis of organelles such as melanosomes and platelet-dense granules. A mouse model for Hermansky-Pudlak Syndrome is mutated in the murine version of this gene. Alternative splicing results in multiple transcript variants. Read-through transcription exists between this gene and the upstream EEF1E1 (eukaryotic translation elongation factor 1 epsilon 1) gene, as well as with the downstream TXNDC5 (thioredoxin domain containing 5) gene. [provided by RefSeq, Dec 2010]","start":8013567,"end":8064414,"strand":-1,"description":"biogenesis of lysosomal organelles complex 1 subunit 5 [Source:HGNC Symbol;Acc:HGNC:18561]"}, {"versioned_ensembl_gene_id":"ENSG00000243721.1","gene_symbol":"RPL23AP63","gene_name":"ribosomal protein L23a pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35502]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729798","summary":null,"start":43718676,"end":43719146,"strand":1,"description":"ribosomal protein L23a pseudogene 63 [Source:HGNC Symbol;Acc:HGNC:35502]"}, {"versioned_ensembl_gene_id":"ENSG00000173391.8","gene_symbol":"OLR1","gene_name":"oxidized low density lipoprotein receptor 1 [Source:HGNC Symbol;Acc:HGNC:8133]","synonyms":"SCARE1,LOX-1,CLEC8A","biotype":"protein_coding","ncbi_id":"4973","summary":"This gene encodes a low density lipoprotein receptor that belongs to the C-type lectin superfamily. This gene is regulated through the cyclic AMP signaling pathway. The encoded protein binds, internalizes and degrades oxidized low-density lipoprotein. This protein may be involved in the regulation of Fas-induced apoptosis. This protein may play a role as a scavenger receptor. Mutations of this gene have been associated with atherosclerosis, risk of myocardial infarction, and may modify the risk of Alzheimer's disease. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]","start":10158301,"end":10172138,"strand":-1,"description":"oxidized low density lipoprotein receptor 1 [Source:HGNC Symbol;Acc:HGNC:8133]"}, {"versioned_ensembl_gene_id":"ENSG00000235943.1","gene_symbol":"TMEM212-IT1","gene_name":"TMEM212 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41505]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874359","summary":null,"start":171894436,"end":171895240,"strand":1,"description":"TMEM212 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41505]"}, {"versioned_ensembl_gene_id":"ENSG00000256571.1","gene_symbol":"AC079866.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":63878787,"end":63879474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000246250.2","gene_symbol":"AC087521.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43829709,"end":43880726,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065802.11","gene_symbol":"ASB1","gene_name":"ankyrin repeat and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:16011]","synonyms":"ASB-1","biotype":"protein_coding","ncbi_id":"51665","summary":"The protein encoded by this gene contains an ankyrin repeat sequence and SOCS box domain. The SOCS box serves to couple suppressor of cytokine signalling (SOCS) proteins and their binding partners with the elongin B and C complex, targeting them for ubiquitination and degradation. [provided by RefSeq, Aug 2016]","start":238426742,"end":238452250,"strand":1,"description":"ankyrin repeat and SOCS box containing 1 [Source:HGNC Symbol;Acc:HGNC:16011]"}, {"versioned_ensembl_gene_id":"ENSG00000149084.12","gene_symbol":"HSD17B12","gene_name":"hydroxysteroid 17-beta dehydrogenase 12 [Source:HGNC Symbol;Acc:HGNC:18646]","synonyms":"SDR12C1,KAR","biotype":"protein_coding","ncbi_id":"51144","summary":"This gene encodes a very important 17beta-hydroxysteroid dehydrogenase (17beta-HSD) that converts estrone into estradiol in ovarian tissue. This enzyme is also involved in fatty acid elongation. [provided by RefSeq, Oct 2011]","start":43680558,"end":43856617,"strand":1,"description":"hydroxysteroid 17-beta dehydrogenase 12 [Source:HGNC Symbol;Acc:HGNC:18646]"}, {"versioned_ensembl_gene_id":"ENSG00000131791.7","gene_symbol":"PRKAB2","gene_name":"protein kinase AMP-activated non-catalytic subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:9379]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5565","summary":"The protein encoded by this gene is a regulatory subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This subunit may be a positive regulator of AMPK activity. It is highly expressed in skeletal muscle and thus may have tissue-specific roles. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2013]","start":147155106,"end":147172550,"strand":-1,"description":"protein kinase AMP-activated non-catalytic subunit beta 2 [Source:HGNC Symbol;Acc:HGNC:9379]"}, {"versioned_ensembl_gene_id":"ENSG00000255817.1","gene_symbol":"AC025576.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64108763,"end":64120489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242087.2","gene_symbol":"RPL36AP41","gene_name":"ribosomal protein L36a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35813]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271644","summary":null,"start":63871739,"end":63872044,"strand":-1,"description":"ribosomal protein L36a pseudogene 41 [Source:HGNC Symbol;Acc:HGNC:35813]"}, {"versioned_ensembl_gene_id":"ENSG00000282965.1","gene_symbol":"AP001005.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49815,"end":73545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251229.1","gene_symbol":"AL645924.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":2505081,"end":2506279,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255780.1","gene_symbol":"AC020611.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64032412,"end":64032665,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205452.4","gene_symbol":"AC133561.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":33972912,"end":33976346,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256399.1","gene_symbol":"AC079866.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":63887379,"end":63888598,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206113.10","gene_symbol":"CFAP99","gene_name":"cilia and flagella associated protein 99 [Source:HGNC Symbol;Acc:HGNC:51180]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402160","summary":null,"start":2418974,"end":2462942,"strand":1,"description":"cilia and flagella associated protein 99 [Source:HGNC Symbol;Acc:HGNC:51180]"}, {"versioned_ensembl_gene_id":"ENSG00000196935.8","gene_symbol":"SRGAP1","gene_name":"SLIT-ROBO Rho GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:17382]","synonyms":"KIAA1304,ARHGAP13","biotype":"protein_coding","ncbi_id":"57522","summary":"The protein encoded by this gene is a GTPase activator, working with the GTPase CDC42 to negatively regulate neuronal migration. The encoded protein interacts with the transmembrane receptor ROBO1 to inactivate CDC42. [provided by RefSeq, Sep 2016]","start":63844293,"end":64162221,"strand":1,"description":"SLIT-ROBO Rho GTPase activating protein 1 [Source:HGNC Symbol;Acc:HGNC:17382]"}, {"versioned_ensembl_gene_id":"ENSG00000272888.5","gene_symbol":"LINC01578","gene_name":"long intergenic non-protein coding RNA 1578 [Source:HGNC Symbol;Acc:HGNC:48626]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100507217","summary":null,"start":92882707,"end":92899701,"strand":1,"description":"long intergenic non-protein coding RNA 1578 [Source:HGNC Symbol;Acc:HGNC:48626]"}, {"versioned_ensembl_gene_id":"ENSG00000198555.7","gene_symbol":"AC133561.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":33976039,"end":33987630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100325.14","gene_symbol":"ASCC2","gene_name":"activating signal cointegrator 1 complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24103]","synonyms":"FLJ21588,DKFZp586O0223,ASC1p100","biotype":"protein_coding","ncbi_id":"84164","summary":null,"start":29788608,"end":29838304,"strand":-1,"description":"activating signal cointegrator 1 complex subunit 2 [Source:HGNC Symbol;Acc:HGNC:24103]"}, {"versioned_ensembl_gene_id":"ENSG00000262050.1","gene_symbol":"AC005696.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2712309,"end":2712833,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139597.17","gene_symbol":"N4BP2L1","gene_name":"NEDD4 binding protein 2 like 1 [Source:HGNC Symbol;Acc:HGNC:25037]","synonyms":"CG018","biotype":"protein_coding","ncbi_id":"90634","summary":null,"start":32400723,"end":32428311,"strand":-1,"description":"NEDD4 binding protein 2 like 1 [Source:HGNC Symbol;Acc:HGNC:25037]"}, {"versioned_ensembl_gene_id":"ENSG00000171658.8","gene_symbol":"NMRAL2P","gene_name":"NmrA like redox sensor 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:52332]","synonyms":"NMRAL1P1,LOC344887","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"344887","summary":null,"start":185959943,"end":185980872,"strand":1,"description":"NmrA like redox sensor 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:52332]"}, {"versioned_ensembl_gene_id":"ENSG00000225611.1","gene_symbol":"LINC02158","gene_name":"long intergenic non-protein coding RNA 2158 [Source:HGNC Symbol;Acc:HGNC:53019]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"729083","summary":null,"start":42770612,"end":42773635,"strand":1,"description":"long intergenic non-protein coding RNA 2158 [Source:HGNC Symbol;Acc:HGNC:53019]"}, {"versioned_ensembl_gene_id":"ENSG00000144649.8","gene_symbol":"FAM198A","gene_name":"family with sequence similarity 198 member A [Source:HGNC Symbol;Acc:HGNC:24485]","synonyms":"DKFZP434B172,C3orf41","biotype":"protein_coding","ncbi_id":"729085","summary":null,"start":42979267,"end":43060211,"strand":1,"description":"family with sequence similarity 198 member A [Source:HGNC Symbol;Acc:HGNC:24485]"}, {"versioned_ensembl_gene_id":"ENSG00000001626.14","gene_symbol":"CFTR","gene_name":"cystic fibrosis transmembrane conductance regulator [Source:HGNC Symbol;Acc:HGNC:1884]","synonyms":"CF,ABCC7,ABC35,TNR-CFTR,MRP7,dJ760C5.1,CFTR/MRP","biotype":"protein_coding","ncbi_id":"1080","summary":"This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome. [provided by RefSeq, Aug 2017]","start":117465784,"end":117715971,"strand":1,"description":"cystic fibrosis transmembrane conductance regulator [Source:HGNC Symbol;Acc:HGNC:1884]"}, {"versioned_ensembl_gene_id":"ENSG00000232378.1","gene_symbol":"RPL29P28","gene_name":"ribosomal protein L29 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36842]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646884","summary":null,"start":36926438,"end":36927219,"strand":-1,"description":"ribosomal protein L29 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:36842]"}, {"versioned_ensembl_gene_id":"ENSG00000271302.1","gene_symbol":"AC105254.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121118299,"end":121118734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257976.1","gene_symbol":"AL079352.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25431193,"end":25432234,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125386.15","gene_symbol":"FAM193A","gene_name":"family with sequence similarity 193 member A [Source:HGNC Symbol;Acc:HGNC:16822]","synonyms":"RES4-22,C4orf8","biotype":"protein_coding","ncbi_id":"8603","summary":null,"start":2536631,"end":2732565,"strand":1,"description":"family with sequence similarity 193 member A [Source:HGNC Symbol;Acc:HGNC:16822]"}, {"versioned_ensembl_gene_id":"ENSG00000112561.17","gene_symbol":"TFEB","gene_name":"transcription factor EB [Source:HGNC Symbol;Acc:HGNC:11753]","synonyms":"bHLHe35,TCFEB","biotype":"protein_coding","ncbi_id":"7942","summary":null,"start":41683978,"end":41736259,"strand":-1,"description":"transcription factor EB [Source:HGNC Symbol;Acc:HGNC:11753]"}, {"versioned_ensembl_gene_id":"ENSG00000232828.1","gene_symbol":"AC231533.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48698963,"end":48737163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259727.1","gene_symbol":"AC103740.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62895812,"end":62899543,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189229.10","gene_symbol":"AC069277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6490479,"end":6736129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124802.11","gene_symbol":"EEF1E1","gene_name":"eukaryotic translation elongation factor 1 epsilon 1 [Source:HGNC Symbol;Acc:HGNC:3212]","synonyms":"P18,AIMP3","biotype":"protein_coding","ncbi_id":"9521","summary":"This gene encodes a multifunctional protein that localizes to both the cytoplasm and nucleus. In the cytoplasm, the encoded protein is an auxiliary component of the macromolecular aminoacyl-tRNA synthase complex. However, its mouse homolog has been shown to translocate to the nucleus in response to DNA damage, and it plays a positive role in ATM/ATR-mediated p53 activation. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring downstream MUTED (muted homolog) gene. An EEF1E1-related pseudogene has been identified on chromosome 2. [provided by RefSeq, Dec 2010]","start":8073360,"end":8102578,"strand":-1,"description":"eukaryotic translation elongation factor 1 epsilon 1 [Source:HGNC Symbol;Acc:HGNC:3212]"}, {"versioned_ensembl_gene_id":"ENSG00000276504.4","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"FB1,INO80F,INO80F,amida,amida,FB1","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000173575.20","gene_symbol":"CHD2","gene_name":"chromodomain helicase DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1917]","synonyms":"FLJ38614,DKFZp781D1727,DKFZp686E01200,DKFZp547I1315","biotype":"protein_coding","ncbi_id":"1106","summary":"The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":92900189,"end":93028005,"strand":1,"description":"chromodomain helicase DNA binding protein 2 [Source:HGNC Symbol;Acc:HGNC:1917]"}, {"versioned_ensembl_gene_id":"ENSG00000260859.1","gene_symbol":"AC025280.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":84828263,"end":84829242,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279622.1","gene_symbol":"AC025280.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":84917377,"end":84919923,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103196.11","gene_symbol":"CRISPLD2","gene_name":"cysteine rich secretory protein LCCL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25248]","synonyms":"LGL1,LCRISP2,DKFZP434B044","biotype":"protein_coding","ncbi_id":"83716","summary":null,"start":84819984,"end":84920768,"strand":1,"description":"cysteine rich secretory protein LCCL domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25248]"}, {"versioned_ensembl_gene_id":"ENSG00000273726.1","gene_symbol":"CU104682.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54268639,"end":54269669,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187792.4","gene_symbol":"ZNF70","gene_name":"zinc finger protein 70 [Source:HGNC Symbol;Acc:HGNC:13140]","synonyms":"MGC48959,Cos17","biotype":"protein_coding","ncbi_id":"7621","summary":null,"start":23738678,"end":23751092,"strand":-1,"description":"zinc finger protein 70 [Source:HGNC Symbol;Acc:HGNC:13140]"}, {"versioned_ensembl_gene_id":"ENSG00000246339.5","gene_symbol":"EXTL3-AS1","gene_name":"EXTL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27985]","synonyms":"C8orf50","biotype":"antisense_RNA","ncbi_id":"101929402","summary":null,"start":28696198,"end":28701464,"strand":-1,"description":"EXTL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27985]"}, {"versioned_ensembl_gene_id":"ENSG00000181061.13","gene_symbol":"HIGD1A","gene_name":"HIG1 hypoxia inducible domain family member 1A [Source:HGNC Symbol;Acc:HGNC:29527]","synonyms":"DKFZP564K247,RCF1A,HIG1","biotype":"protein_coding","ncbi_id":"25994","summary":null,"start":42784298,"end":42804531,"strand":-1,"description":"HIG1 hypoxia inducible domain family member 1A [Source:HGNC Symbol;Acc:HGNC:29527]"}, {"versioned_ensembl_gene_id":"ENSG00000012232.8","gene_symbol":"EXTL3","gene_name":"exostosin like glycosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:3518]","synonyms":"REGR,botv","biotype":"protein_coding","ncbi_id":"2137","summary":"This gene encodes a single-pass membrane protein which functions as a glycosyltransferase. The encoded protein catalyzes the transfer of N-acetylglucosamine to glycosaminoglycan chains. This reaction is important in heparin and heparan sulfate synthesis. Alternative splicing results in the multiple transcript variants. [provided by RefSeq, Nov 2012]","start":28600469,"end":28755599,"strand":1,"description":"exostosin like glycosyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:3518]"}, {"versioned_ensembl_gene_id":"ENSG00000128218.7","gene_symbol":"VPREB3","gene_name":"V-set pre-B cell surrogate light chain 3 [Source:HGNC Symbol;Acc:HGNC:12710]","synonyms":"8HS20","biotype":"protein_coding","ncbi_id":"29802","summary":"The protein encoded by this gene is the human ortholog of the mouse VpreB3 (8HS20) protein, is thought to be involved in B-cell maturation, and may play a role in assembly of the pre-B cell receptor (pre-BCR). While the role of this protein in B-cell development has not yet been elucidated, studies with the chicken ortholog of this protein have found that when overexpressed, this protein localizes to the endoplasmic reticulum. The mouse ortholog of this protein has been shown to associate with membrane mu heavy chains early in the course of pre-B cell receptor biosynthesis. Expression of this gene has been observed in some lymphomas. [provided by RefSeq, Apr 2015]","start":23752743,"end":23754468,"strand":-1,"description":"V-set pre-B cell surrogate light chain 3 [Source:HGNC Symbol;Acc:HGNC:12710]"}, {"versioned_ensembl_gene_id":"ENSG00000270210.1","gene_symbol":"AC104695.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28425945,"end":28426719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256433.2","gene_symbol":"AC005840.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6393905,"end":6396148,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276627.1","gene_symbol":"AL117372.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60761874,"end":60767279,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227938.1","gene_symbol":"AC104695.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28448167,"end":28450184,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217746.1","gene_symbol":"AL096800.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7938430,"end":7939322,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257285.5","gene_symbol":"AL132780.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22929609,"end":22955562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000219941.1","gene_symbol":"KRT18P50","gene_name":"keratin 18 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:33420]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442236","summary":null,"start":95991107,"end":95992349,"strand":1,"description":"keratin 18 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:33420]"}, {"versioned_ensembl_gene_id":"ENSG00000120937.8","gene_symbol":"NPPB","gene_name":"natriuretic peptide B [Source:HGNC Symbol;Acc:HGNC:7940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4879","summary":"This gene is a member of the natriuretic peptide family and encodes a secreted protein which functions as a cardiac hormone. The protein undergoes two cleavage events, one within the cell and a second after secretion into the blood. The protein's biological actions include natriuresis, diuresis, vasorelaxation, inhibition of renin and aldosterone secretion, and a key role in cardiovascular homeostasis. A high concentration of this protein in the bloodstream is indicative of heart failure. The presence of myocardial injury is a significant predictor of mortality in hospitalized coronavirus disease 2019 (COVID-19) patients, and there is evidence of increased levels of natriuretic peptide B in hospitalized non-survivor COVID-19 patients. The protein also acts as an antimicrobial peptide with antibacterial and antifungal activity. Mutations in this gene have been associated with postmenopausal osteoporosis. [provided by RefSeq, Aug 2020]","start":11857464,"end":11858931,"strand":-1,"description":"natriuretic peptide B [Source:HGNC Symbol;Acc:HGNC:7940]"}, {"versioned_ensembl_gene_id":"ENSG00000109881.16","gene_symbol":"CCDC34","gene_name":"coiled-coil domain containing 34 [Source:HGNC Symbol;Acc:HGNC:25079]","synonyms":"RAMA3,NY-REN-41,L15","biotype":"protein_coding","ncbi_id":"91057","summary":null,"start":27330827,"end":27363868,"strand":-1,"description":"coiled-coil domain containing 34 [Source:HGNC Symbol;Acc:HGNC:25079]"}, {"versioned_ensembl_gene_id":"ENSG00000239264.8","gene_symbol":"TXNDC5","gene_name":"thioredoxin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21073]","synonyms":"FLJ90810,FLJ21353,ERp46,EndoPDI,PDIA15,MGC3178,Hcc-2","biotype":"protein_coding","ncbi_id":"81567","summary":"This gene encodes a member of the disulfide isomerase (PDI) family of endoplasmic reticulum (ER) proteins that catalyze protein folding and thiol-disulfide interchange reactions. The encoded protein has an N-terminal endoplasmic reticulum (ER)-signal sequence, three catalytically active thioredoxin domains and a C-terminal ER-retention sequence. Its expression is induced by hypoxia and its role may be to protect hypoxic cells from apoptosis. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S5 gene. [provided by RefSeq, Dec 2016]","start":7881517,"end":7910814,"strand":-1,"description":"thioredoxin domain containing 5 [Source:HGNC Symbol;Acc:HGNC:21073]"}, {"versioned_ensembl_gene_id":"ENSG00000079393.20","gene_symbol":"DUSP13","gene_name":"dual specificity phosphatase 13 [Source:HGNC Symbol;Acc:HGNC:19681]","synonyms":"TMDP,FLJ32450,DUSP13B,DUSP13A,BEDP","biotype":"protein_coding","ncbi_id":"51207","summary":"Members of the protein-tyrosine phosphatase superfamily cooperate with protein kinases to regulate cell proliferation and differentiation. This superfamily is separated into two families based on the substrate that is dephosphorylated. One family, the dual specificity phosphatases (DSPs) acts on both phosphotyrosine and phosphoserine/threonine residues. This gene encodes different but related DSP proteins through the use of non-overlapping open reading frames, alternate splicing, and presumed different transcription promoters. Expression of the distinct proteins from this gene has been found to be tissue specific and the proteins may be involved in postnatal development of specific tissues. A protein encoded by the upstream ORF was found in skeletal muscle, whereas the encoded protein from the downstream ORF was found only in testis. In mouse, a similar pattern of expression was found. Multiple alternatively spliced transcript variants were described, but the full-length sequence of only some were determined. [provided by RefSeq, Jul 2008]","start":75094432,"end":75109221,"strand":-1,"description":"dual specificity phosphatase 13 [Source:HGNC Symbol;Acc:HGNC:19681]"}, {"versioned_ensembl_gene_id":"ENSG00000164823.9","gene_symbol":"OSGIN2","gene_name":"oxidative stress induced growth inhibitor family member 2 [Source:HGNC Symbol;Acc:HGNC:1355]","synonyms":"hT41,C8orf1","biotype":"protein_coding","ncbi_id":"734","summary":null,"start":89901859,"end":89927888,"strand":1,"description":"oxidative stress induced growth inhibitor family member 2 [Source:HGNC Symbol;Acc:HGNC:1355]"}, {"versioned_ensembl_gene_id":"ENSG00000259132.1","gene_symbol":"AL132780.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22946270,"end":22982258,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213942.3","gene_symbol":"AC005840.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6409637,"end":6410013,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000092036.18","gene_symbol":"HAUS4","gene_name":"HAUS augmin like complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:20163]","synonyms":"FLJ20424,C14orf94","biotype":"protein_coding","ncbi_id":"54930","summary":"This gene encodes a subunit of the centrosome complex termed the human augmin complex. The encoded protein localizes to the spindle microtubules and may play a role in mitotic spindle assembly and maintenance of centrosome integrity during cell division. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 1. [provided by RefSeq, Oct 2009]","start":22946228,"end":22957161,"strand":-1,"description":"HAUS augmin like complex subunit 4 [Source:HGNC Symbol;Acc:HGNC:20163]"}, {"versioned_ensembl_gene_id":"ENSG00000166961.14","gene_symbol":"MS4A15","gene_name":"membrane spanning 4-domains A15 [Source:HGNC Symbol;Acc:HGNC:28573]","synonyms":null,"biotype":"protein_coding","ncbi_id":"219995","summary":null,"start":60756953,"end":60776732,"strand":1,"description":"membrane spanning 4-domains A15 [Source:HGNC Symbol;Acc:HGNC:28573]"}, {"versioned_ensembl_gene_id":"ENSG00000224906.3","gene_symbol":"AC005840.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6438498,"end":6438852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224904.1","gene_symbol":"AL021155.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":11877770,"end":11880406,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250479.8","gene_symbol":"CHCHD10","gene_name":"coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]","synonyms":"N27C7-4,C22orf16","biotype":"protein_coding","ncbi_id":"400916","summary":"This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19. [provided by RefSeq, Aug 2014]","start":23765834,"end":23768443,"strand":-1,"description":"coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]"}, {"versioned_ensembl_gene_id":"ENSG00000116685.15","gene_symbol":"KIAA2013","gene_name":"KIAA2013 [Source:HGNC Symbol;Acc:HGNC:28513]","synonyms":"RP5-1077B9.1,MGC33867","biotype":"protein_coding","ncbi_id":"90231","summary":null,"start":11919591,"end":11926428,"strand":-1,"description":"KIAA2013 [Source:HGNC Symbol;Acc:HGNC:28513]"}, {"versioned_ensembl_gene_id":"ENSG00000283341.1","gene_symbol":"AC068205.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":43578889,"end":43840030,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261035.1","gene_symbol":"AL139348.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60812004,"end":60814211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224672.4","gene_symbol":"RPL17P10","gene_name":"ribosomal protein L17 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35838]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270936","summary":null,"start":201102089,"end":201102957,"strand":-1,"description":"ribosomal protein L17 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:35838]"}, {"versioned_ensembl_gene_id":"ENSG00000232719.1","gene_symbol":"AC007272.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":201101382,"end":201103136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000099953.9","gene_symbol":"MMP11","gene_name":"matrix metallopeptidase 11 [Source:HGNC Symbol;Acc:HGNC:7157]","synonyms":"STMY3","biotype":"protein_coding","ncbi_id":"4320","summary":"Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the enzyme encoded by this gene is activated intracellularly by furin within the constitutive secretory pathway. Also in contrast to other MMP's, this enzyme cleaves alpha 1-proteinase inhibitor but weakly degrades structural proteins of the extracellular matrix. [provided by RefSeq, Jul 2008]","start":23768226,"end":23784316,"strand":1,"description":"matrix metallopeptidase 11 [Source:HGNC Symbol;Acc:HGNC:7157]"}, {"versioned_ensembl_gene_id":"ENSG00000229755.1","gene_symbol":"AL121910.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61077224,"end":61077816,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233764.1","gene_symbol":"MTCO1P20","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52085]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075163","summary":null,"start":36172422,"end":36172779,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52085]"}, {"versioned_ensembl_gene_id":"ENSG00000144648.15","gene_symbol":"ACKR2","gene_name":"atypical chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:1565]","synonyms":"D6,CMKBR9,CCR9,CCR10,CCBP2","biotype":"protein_coding","ncbi_id":"1238","summary":"This gene encodes a beta chemokine receptor, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. Chemokines and their receptor-mediated signal transduction are critical for the recruitment of effector immune cells to the inflammation site. This gene is expressed in a range of tissues and hemopoietic cells. The expression of this receptor in lymphatic endothelial cells and overexpression in vascular tumors suggested its function in chemokine-driven recirculation of leukocytes and possible chemokine effects on the development and growth of vascular tumors. This receptor appears to bind the majority of beta-chemokine family members; however, its specific function remains unknown. This gene is mapped to chromosome 3p21.3, a region that includes a cluster of chemokine receptor genes. [provided by RefSeq, Jul 2008]","start":42804752,"end":42887974,"strand":1,"description":"atypical chemokine receptor 2 [Source:HGNC Symbol;Acc:HGNC:1565]"}, {"versioned_ensembl_gene_id":"ENSG00000283393.1","gene_symbol":"AC068205.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43718676,"end":43719143,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283375.1","gene_symbol":"AC087521.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":43855913,"end":43856404,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231576.1","gene_symbol":"MTCO2P20","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075230","summary":null,"start":36172934,"end":36173948,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52149]"}, {"versioned_ensembl_gene_id":"ENSG00000283483.1","gene_symbol":"AC068205.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43733761,"end":43734564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251197.1","gene_symbol":"MICE","gene_name":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]","synonyms":"PERB11.5,dJ377H14.7","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"4280","summary":null,"start":29739180,"end":29746420,"strand":-1,"description":"MHC class I polypeptide-related sequence E (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7094]"}, {"versioned_ensembl_gene_id":"ENSG00000235661.3","gene_symbol":"MIR670HG","gene_name":"MIR670 host gene [Source:HGNC Symbol;Acc:HGNC:49204]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507261","summary":null,"start":43569306,"end":43570395,"strand":1,"description":"MIR670 host gene [Source:HGNC Symbol;Acc:HGNC:49204]"}, {"versioned_ensembl_gene_id":"ENSG00000255629.1","gene_symbol":"AC025576.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64146388,"end":64147857,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275145.3","gene_symbol":"FRG1","gene_name":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]","synonyms":"FSG1,FRG1A","biotype":"protein_coding","ncbi_id":"2483","summary":"This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]","start":189944765,"end":189967182,"strand":1,"description":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]"}, {"versioned_ensembl_gene_id":"ENSG00000255886.1","gene_symbol":"AC020611.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":64038562,"end":64097618,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186329.9","gene_symbol":"TMEM212","gene_name":"transmembrane protein 212 [Source:HGNC Symbol;Acc:HGNC:34295]","synonyms":"FLJ23172","biotype":"protein_coding","ncbi_id":"389177","summary":null,"start":171843349,"end":171938715,"strand":1,"description":"transmembrane protein 212 [Source:HGNC Symbol;Acc:HGNC:34295]"}, {"versioned_ensembl_gene_id":"ENSG00000264490.3","gene_symbol":"BX640514.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62575590,"end":62577507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266389.1","gene_symbol":"AC002091.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8965896,"end":8967070,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131781.12","gene_symbol":"FMO5","gene_name":"flavin containing monooxygenase 5 [Source:HGNC Symbol;Acc:HGNC:3773]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2330","summary":"Metabolic N-oxidation of the diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man resulting in a small subpopulation with reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found in adult liver, and FMO3 are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":147175351,"end":147243050,"strand":-1,"description":"flavin containing monooxygenase 5 [Source:HGNC Symbol;Acc:HGNC:3773]"}, {"versioned_ensembl_gene_id":"ENSG00000265975.1","gene_symbol":"AC002091.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8967523,"end":8976995,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237948.1","gene_symbol":"MTATP6P20","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52176]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075201","summary":null,"start":36174261,"end":36174822,"strand":1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52176]"}, {"versioned_ensembl_gene_id":"ENSG00000238026.1","gene_symbol":"AC117434.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":176113702,"end":176114537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254512.1","gene_symbol":"PHBP2","gene_name":"prohibitin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8914]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418837","summary":null,"start":43733759,"end":43734564,"strand":1,"description":"prohibitin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:8914]"}, {"versioned_ensembl_gene_id":"ENSG00000225557.1","gene_symbol":"MTCO3P20","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52122]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075180","summary":null,"start":36175167,"end":36175854,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:52122]"}, {"versioned_ensembl_gene_id":"ENSG00000283217.1","gene_symbol":"AC068205.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43556436,"end":43673393,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273812.1","gene_symbol":"BX640514.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62596732,"end":62603115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274041.1","gene_symbol":"AC012314.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54119637,"end":54125468,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237129.1","gene_symbol":"MTCYBP34","gene_name":"mitochondrially encoded cytochrome b pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:52302]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729115","summary":null,"start":36175857,"end":36176526,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 34 [Source:HGNC Symbol;Acc:HGNC:52302]"}, {"versioned_ensembl_gene_id":"ENSG00000270008.1","gene_symbol":"AL137247.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":32425358,"end":32432954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165097.13","gene_symbol":"KDM1B","gene_name":"lysine demethylase 1B [Source:HGNC Symbol;Acc:HGNC:21577]","synonyms":"FLJ34109,FLJ33898,dJ298J15.2,C6orf193,bA204B7.3,AOF1,LSD2,FLJ43328","biotype":"protein_coding","ncbi_id":"221656","summary":"Flavin-dependent histone demethylases, such as KDM1B, regulate histone lysine methylation, an epigenetic mark that regulates gene expression and chromatin function (Karytinos et al., 2009 [PubMed 19407342]).[supplied by OMIM, Oct 2009]","start":18155329,"end":18223853,"strand":1,"description":"lysine demethylase 1B [Source:HGNC Symbol;Acc:HGNC:21577]"}, {"versioned_ensembl_gene_id":"ENSG00000166090.8","gene_symbol":"IL25","gene_name":"interleukin 25 [Source:HGNC Symbol;Acc:HGNC:13765]","synonyms":"IL17E,IL-25,IL-17E","biotype":"protein_coding","ncbi_id":"64806","summary":"The protein encoded by this gene is a cytokine that shares sequence similarity with interleukin 17. This cytokine can induce NF-kappaB activation, and stimulate the production of interleukin 8. Both this cytokine and interleukin 17B are ligands for the cytokine receptor IL17BR. Studies of a similar gene in mice suggest that this cytokine may be a pro-inflammatory cytokine favoring the Th2-type immune response. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":23372809,"end":23376403,"strand":1,"description":"interleukin 25 [Source:HGNC Symbol;Acc:HGNC:13765]"}, {"versioned_ensembl_gene_id":"ENSG00000229800.1","gene_symbol":"ATP8A2P2","gene_name":"ATPase phospholipid transporting 8A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39663]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533851","summary":null,"start":32477274,"end":32478841,"strand":1,"description":"ATPase phospholipid transporting 8A2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39663]"}, {"versioned_ensembl_gene_id":"ENSG00000229882.1","gene_symbol":"AL450469.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62633772,"end":62635862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275885.4","gene_symbol":"PRPF31","gene_name":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]","synonyms":"RP11,NY-BR-99,NY-BR-99,SNRNP61,SNRNP61,PRP31,PRP31,hPrp31,hPrp31,RP11","biotype":"protein_coding","ncbi_id":"26121","summary":"This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]","start":54115536,"end":54131896,"strand":1,"description":"pre-mRNA processing factor 31 [Source:HGNC Symbol;Acc:HGNC:15446]"}, {"versioned_ensembl_gene_id":"ENSG00000229088.1","gene_symbol":"MTND1P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42097]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873343","summary":null,"start":36178554,"end":36179385,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42097]"}, {"versioned_ensembl_gene_id":"ENSG00000232121.1","gene_symbol":"AL450469.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62633681,"end":62635504,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184281.14","gene_symbol":"TSSC4","gene_name":"tumor suppressing subtransferable candidate 4 [Source:HGNC Symbol;Acc:HGNC:12386]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10078","summary":"This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the pan-hematopoietic expression gene (PHEMX), escapes imprinting. This gene may play a role in malignancies and disease that involve this region. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":2400488,"end":2403878,"strand":1,"description":"tumor suppressing subtransferable candidate 4 [Source:HGNC Symbol;Acc:HGNC:12386]"}, {"versioned_ensembl_gene_id":"ENSG00000234717.1","gene_symbol":"TMEM212-AS1","gene_name":"TMEM212 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41939]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874219","summary":null,"start":171876352,"end":171900740,"strand":-1,"description":"TMEM212 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41939]"}, {"versioned_ensembl_gene_id":"ENSG00000223715.1","gene_symbol":"LINC01208","gene_name":"long intergenic non-protein coding RNA 1208 [Source:HGNC Symbol;Acc:HGNC:49639]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505547","summary":null,"start":176604143,"end":176635532,"strand":-1,"description":"long intergenic non-protein coding RNA 1208 [Source:HGNC Symbol;Acc:HGNC:49639]"}, {"versioned_ensembl_gene_id":"ENSG00000229606.1","gene_symbol":"LINC01718","gene_name":"long intergenic non-protein coding RNA 1718 [Source:HGNC Symbol;Acc:HGNC:52505]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506470","summary":null,"start":61079140,"end":61080179,"strand":1,"description":"long intergenic non-protein coding RNA 1718 [Source:HGNC Symbol;Acc:HGNC:52505]"}, {"versioned_ensembl_gene_id":"ENSG00000274723.1","gene_symbol":"AC079906.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":46970504,"end":46972155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146733.13","gene_symbol":"PSPH","gene_name":"phosphoserine phosphatase [Source:HGNC Symbol;Acc:HGNC:9577]","synonyms":"PSP","biotype":"protein_coding","ncbi_id":"5723","summary":"The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]","start":56011051,"end":56051604,"strand":-1,"description":"phosphoserine phosphatase [Source:HGNC Symbol;Acc:HGNC:9577]"}, {"versioned_ensembl_gene_id":"ENSG00000279521.1","gene_symbol":"AL359396.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25820366,"end":25822741,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114993.16","gene_symbol":"RTKN","gene_name":"rhotekin [Source:HGNC Symbol;Acc:HGNC:10466]","synonyms":"B5","biotype":"protein_coding","ncbi_id":"6242","summary":"This gene encodes a scaffold protein that interacts with GTP-bound Rho proteins. Binding of this protein inhibits the GTPase activity of Rho proteins. This protein may interfere with the conversion of active, GTP-bound Rho to the inactive GDP-bound form by RhoGAP. Rho proteins regulate many important cellular processes, including cytokinesis, transcription, smooth muscle contraction, cell growth and transformation. Dysregulation of the Rho signal transduction pathway has been implicated in many forms of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":74425836,"end":74442422,"strand":-1,"description":"rhotekin [Source:HGNC Symbol;Acc:HGNC:10466]"}, {"versioned_ensembl_gene_id":"ENSG00000271787.1","gene_symbol":"AC104794.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10054421,"end":10054866,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172059.10","gene_symbol":"KLF11","gene_name":"Kruppel like factor 11 [Source:HGNC Symbol;Acc:HGNC:11811]","synonyms":"TIEG2,MODY7,Tieg3","biotype":"protein_coding","ncbi_id":"8462","summary":"The protein encoded by this gene is a zinc finger transcription factor that binds to SP1-like sequences in epsilon- and gamma-globin gene promoters. This binding inhibits cell growth and causes apoptosis. Defects in this gene are a cause of maturity-onset diabetes of the young type 7 (MODY7). Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]","start":10042849,"end":10054836,"strand":1,"description":"Kruppel like factor 11 [Source:HGNC Symbol;Acc:HGNC:11811]"}, {"versioned_ensembl_gene_id":"ENSG00000272308.1","gene_symbol":"AC104113.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":60866457,"end":60866935,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273328.5","gene_symbol":"AC099329.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":42809414,"end":42908105,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270207.1","gene_symbol":"AC068313.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7606890,"end":7607897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257986.1","gene_symbol":"LINC02306","gene_name":"long intergenic non-protein coding RNA 2306 [Source:HGNC Symbol;Acc:HGNC:53225]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107984700","summary":null,"start":25835858,"end":26143305,"strand":-1,"description":"long intergenic non-protein coding RNA 2306 [Source:HGNC Symbol;Acc:HGNC:53225]"}, {"versioned_ensembl_gene_id":"ENSG00000277641.2","gene_symbol":"WNT3","gene_name":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]","synonyms":"INT4,MGC138323,MGC138321,MGC138323,MGC131950,MGC138321,INT4,MGC131950","biotype":"protein_coding","ncbi_id":"7473","summary":"The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 98% amino acid identity to mouse Wnt3 protein, and 84% to human WNT3A protein, another WNT gene product. The mouse studies show the requirement of Wnt3 in primary axis formation in the mouse. Studies of the gene expression suggest that this gene may play a key role in some cases of human breast, rectal, lung, and gastric cancer through activation of the WNT-beta-catenin-TCF signaling pathway. This gene is clustered with WNT15, another family member, in the chromosome 17q21 region. [provided by RefSeq, Jul 2008]","start":46591415,"end":46662074,"strand":-1,"description":"Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]"}, {"versioned_ensembl_gene_id":"ENSG00000226258.6","gene_symbol":"GRM7-AS3","gene_name":"GRM7 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:42444]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927347","summary":null,"start":6631689,"end":6805449,"strand":-1,"description":"GRM7 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:42444]"}, {"versioned_ensembl_gene_id":"ENSG00000010282.14","gene_symbol":"HHATL","gene_name":"hedgehog acyltransferase like [Source:HGNC Symbol;Acc:HGNC:13242]","synonyms":"GUP1,C3orf3,OACT3,MSTP002,MBOAT3,KIAA1173","biotype":"protein_coding","ncbi_id":"57467","summary":null,"start":42692663,"end":42702827,"strand":-1,"description":"hedgehog acyltransferase like [Source:HGNC Symbol;Acc:HGNC:13242]"}, {"versioned_ensembl_gene_id":"ENSG00000257503.1","gene_symbol":"CYB5AP5","gene_name":"cytochrome b5 type A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:2576]","synonyms":"CYB5P5","biotype":"processed_pseudogene","ncbi_id":"100289051","summary":null,"start":26208036,"end":26208424,"strand":1,"description":"cytochrome b5 type A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:2576]"}, {"versioned_ensembl_gene_id":"ENSG00000233252.1","gene_symbol":"CRIP1P1","gene_name":"cysteine rich protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44516]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480793","summary":null,"start":12673699,"end":12673883,"strand":1,"description":"cysteine rich protein 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44516]"}, {"versioned_ensembl_gene_id":"ENSG00000262920.5","gene_symbol":"AC129507.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":321392,"end":322453,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257359.1","gene_symbol":"AC073863.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":113932569,"end":113937255,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262061.5","gene_symbol":"AC129507.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":331205,"end":333488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276317.1","gene_symbol":"AL357033.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62651272,"end":62652186,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122965.10","gene_symbol":"RBM19","gene_name":"RNA binding motif protein 19 [Source:HGNC Symbol;Acc:HGNC:29098]","synonyms":"Mrd1,KIAA0682,DKFZp586F1023","biotype":"protein_coding","ncbi_id":"9904","summary":"This gene encodes a nucleolar protein that contains six RNA-binding motifs. The encoded protein may be involved in regulating ribosome biogenesis. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Apr 2009]","start":113816738,"end":113966371,"strand":-1,"description":"RNA binding motif protein 19 [Source:HGNC Symbol;Acc:HGNC:29098]"}, {"versioned_ensembl_gene_id":"ENSG00000219294.6","gene_symbol":"PIP5K1P1","gene_name":"phosphatidylinositol-4-phosphate 5-kinase type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28372]","synonyms":"MGC26597","biotype":"processed_pseudogene","ncbi_id":"206426","summary":null,"start":7986537,"end":7988192,"strand":1,"description":"phosphatidylinositol-4-phosphate 5-kinase type 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28372]"}, {"versioned_ensembl_gene_id":"ENSG00000262558.1","gene_symbol":"AC129507.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":354737,"end":356882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232803.1","gene_symbol":"SLCO4A1-AS1","gene_name":"SLCO4A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40537]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100127888","summary":null,"start":62663019,"end":62666724,"strand":-1,"description":"SLCO4A1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40537]"}, {"versioned_ensembl_gene_id":"ENSG00000153162.8","gene_symbol":"BMP6","gene_name":"bone morphogenetic protein 6 [Source:HGNC Symbol;Acc:HGNC:1073]","synonyms":"VGR1,VGR","biotype":"protein_coding","ncbi_id":"654","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates a wide range of biological processes including iron homeostasis, fat and bone development, and ovulation. Differential expression of this gene may be associated with progression of breast and prostate cancer. Mutations in this gene may be associated with iron overload in human patients. [provided by RefSeq, Jul 2016]","start":7726797,"end":7881422,"strand":1,"description":"bone morphogenetic protein 6 [Source:HGNC Symbol;Acc:HGNC:1073]"}, {"versioned_ensembl_gene_id":"ENSG00000083622.8","gene_symbol":"AC000061.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":117604791,"end":117647415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274346.1","gene_symbol":"AC016999.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":238454908,"end":238457520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203499.11","gene_symbol":"IQANK1","gene_name":"IQ motif and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:49576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"642574","summary":null,"start":143734140,"end":143790644,"strand":1,"description":"IQ motif and ankyrin repeat containing 1 [Source:HGNC Symbol;Acc:HGNC:49576]"}, {"versioned_ensembl_gene_id":"ENSG00000124356.15","gene_symbol":"STAMBP","gene_name":"STAM binding protein [Source:HGNC Symbol;Acc:HGNC:16950]","synonyms":"AMSH","biotype":"protein_coding","ncbi_id":"10617","summary":"Cytokine-mediated signal transduction in the JAK-STAT cascade requires the involvement of adaptor molecules. One such signal-transducing adaptor molecule contains an SH3 domain that is required for induction of MYC and cell growth. The protein encoded by this gene binds to the SH3 domain of the signal-transducing adaptor molecule, and plays a critical role in cytokine-mediated signaling for MYC induction and cell cycle progression. Multiple alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq, Jul 2008]","start":73828916,"end":73873659,"strand":1,"description":"STAM binding protein [Source:HGNC Symbol;Acc:HGNC:16950]"}, {"versioned_ensembl_gene_id":"ENSG00000276077.4","gene_symbol":"CU633904.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7430659,"end":7469007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181031.15","gene_symbol":"RPH3AL","gene_name":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]","synonyms":"Noc2","biotype":"protein_coding","ncbi_id":"9501","summary":"The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]","start":212389,"end":386254,"strand":-1,"description":"rabphilin 3A like (without C2 domains) [Source:HGNC Symbol;Acc:HGNC:10296]"}, {"versioned_ensembl_gene_id":"ENSG00000242364.1","gene_symbol":"AC108725.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73648399,"end":73648807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268433.1","gene_symbol":"MTDHP3","gene_name":"metadherin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52359]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418832","summary":null,"start":21677550,"end":21678221,"strand":-1,"description":"metadherin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52359]"}, {"versioned_ensembl_gene_id":"ENSG00000225493.1","gene_symbol":"LINC01107","gene_name":"long intergenic non-protein coding RNA 1107 [Source:HGNC Symbol;Acc:HGNC:49229]","synonyms":null,"biotype":"lincRNA","ncbi_id":"151171","summary":null,"start":238510690,"end":238555054,"strand":-1,"description":"long intergenic non-protein coding RNA 1107 [Source:HGNC Symbol;Acc:HGNC:49229]"}, {"versioned_ensembl_gene_id":"ENSG00000268535.1","gene_symbol":"MTDHP4","gene_name":"metadherin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52360]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418834","summary":null,"start":21709522,"end":21710191,"strand":1,"description":"metadherin pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:52360]"}, {"versioned_ensembl_gene_id":"ENSG00000169314.14","gene_symbol":"C22orf15","gene_name":"chromosome 22 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:15558]","synonyms":"FLJ36561,N27C7-3","biotype":"protein_coding","ncbi_id":"150248","summary":null,"start":23763021,"end":23765861,"strand":1,"description":"chromosome 22 open reading frame 15 [Source:HGNC Symbol;Acc:HGNC:15558]"}, {"versioned_ensembl_gene_id":"ENSG00000234279.1","gene_symbol":"LINC01937","gene_name":"long intergenic non-protein coding RNA 1937 [Source:HGNC Symbol;Acc:HGNC:52760]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373962","summary":null,"start":238720324,"end":238740780,"strand":1,"description":"long intergenic non-protein coding RNA 1937 [Source:HGNC Symbol;Acc:HGNC:52760]"}, {"versioned_ensembl_gene_id":"ENSG00000115053.15","gene_symbol":"NCL","gene_name":"nucleolin [Source:HGNC Symbol;Acc:HGNC:7667]","synonyms":"Nsr1,C23","biotype":"protein_coding","ncbi_id":"4691","summary":"Nucleolin (NCL), a eukaryotic nucleolar phosphoprotein, is involved in the synthesis and maturation of ribosomes. It is located mainly in dense fibrillar regions of the nucleolus. Human NCL gene consists of 14 exons with 13 introns and spans approximately 11kb. The intron 11 of the NCL gene encodes a small nucleolar RNA, termed U20. [provided by RefSeq, Jul 2008]","start":231453531,"end":231483641,"strand":-1,"description":"nucleolin [Source:HGNC Symbol;Acc:HGNC:7667]"}, {"versioned_ensembl_gene_id":"ENSG00000224252.1","gene_symbol":"AC113618.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":238735263,"end":238735547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268117.1","gene_symbol":"VN1R84P","gene_name":"vomeronasal 1 receptor 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:37404]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100312829","summary":null,"start":21719801,"end":21720035,"strand":-1,"description":"vomeronasal 1 receptor 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:37404]"}, {"versioned_ensembl_gene_id":"ENSG00000277496.1","gene_symbol":"AL357033.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62648961,"end":62650767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230727.1","gene_symbol":"RBMY2WP","gene_name":"RNA binding motif protein, Y-linked, family 2, member W pseudogene [Source:HGNC Symbol;Acc:HGNC:23900]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"379011","summary":null,"start":22762851,"end":22769787,"strand":-1,"description":"RNA binding motif protein, Y-linked, family 2, member W pseudogene [Source:HGNC Symbol;Acc:HGNC:23900]"}, {"versioned_ensembl_gene_id":"ENSG00000101187.15","gene_symbol":"SLCO4A1","gene_name":"solute carrier organic anion transporter family member 4A1 [Source:HGNC Symbol;Acc:HGNC:10953]","synonyms":"SLC21A12,OATP4A1,OATP-E","biotype":"protein_coding","ncbi_id":"28231","summary":null,"start":62642445,"end":62685785,"strand":1,"description":"solute carrier organic anion transporter family member 4A1 [Source:HGNC Symbol;Acc:HGNC:10953]"}, {"versioned_ensembl_gene_id":"ENSG00000237665.1","gene_symbol":"GRM7-AS2","gene_name":"GRM7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40266]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105376946","summary":null,"start":6892632,"end":6894022,"strand":-1,"description":"GRM7 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:40266]"}, {"versioned_ensembl_gene_id":"ENSG00000147113.16","gene_symbol":"CXorf36","gene_name":"chromosome X open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:25866]","synonyms":"FLJ14103,DIA1R","biotype":"protein_coding","ncbi_id":"79742","summary":null,"start":45148374,"end":45200901,"strand":-1,"description":"chromosome X open reading frame 36 [Source:HGNC Symbol;Acc:HGNC:25866]"}, {"versioned_ensembl_gene_id":"ENSG00000280609.1","gene_symbol":"AL139246.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":2566410,"end":2569888,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223719.1","gene_symbol":"AC069277.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":6692319,"end":6693088,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281740.1","gene_symbol":"AL139246.10","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2581560,"end":2584534,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236152.1","gene_symbol":"MRPS36P1","gene_name":"mitochondrial ribosomal protein S36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29771]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347705","summary":null,"start":6773037,"end":6773343,"strand":-1,"description":"mitochondrial ribosomal protein S36 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29771]"}, {"versioned_ensembl_gene_id":"ENSG00000260926.2","gene_symbol":"AC016134.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41609466,"end":41612727,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233847.1","gene_symbol":"AC022445.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60917490,"end":60919573,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282154.1","gene_symbol":"TRBJ2-6","gene_name":"T-cell receptor beta joining 2-6 [Source:HGNC Symbol;Acc:HGNC:12174]","synonyms":"TRBJ26,TCRBJ2S6","biotype":"TR_J_gene","ncbi_id":"28623","summary":null,"start":142858332,"end":142858384,"strand":1,"description":"T-cell receptor beta joining 2-6 [Source:HGNC Symbol;Acc:HGNC:12174]"}, {"versioned_ensembl_gene_id":"ENSG00000228240.1","gene_symbol":"TTTY17A","gene_name":"testis-specific transcript, Y-linked 17A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18841]","synonyms":"TTTY17,NCRNA00140","biotype":"lincRNA","ncbi_id":"252949","summary":"There are three copies of this gene on chromosome Y. This record represents the most centromeric copy. [provided by RefSeq, Jul 2008]","start":22851584,"end":22852715,"strand":1,"description":"testis-specific transcript, Y-linked 17A (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18841]"}, {"versioned_ensembl_gene_id":"ENSG00000282392.1","gene_symbol":"TRBJ2-7","gene_name":"T-cell receptor beta joining 2-7 [Source:HGNC Symbol;Acc:HGNC:12175]","synonyms":"TRBJ27,TCRBJ2S7","biotype":"TR_J_gene","ncbi_id":"28622","summary":null,"start":142858549,"end":142858595,"strand":1,"description":"T-cell receptor beta joining 2-7 [Source:HGNC Symbol;Acc:HGNC:12175]"}, {"versioned_ensembl_gene_id":"ENSG00000049167.13","gene_symbol":"ERCC8","gene_name":"ERCC excision repair 8, CSA ubiquitin ligase complex subunit [Source:HGNC Symbol;Acc:HGNC:3439]","synonyms":"CSA,CKN1","biotype":"protein_coding","ncbi_id":"1161","summary":"This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]","start":60873831,"end":60945073,"strand":-1,"description":"ERCC excision repair 8, CSA ubiquitin ligase complex subunit [Source:HGNC Symbol;Acc:HGNC:3439]"}, {"versioned_ensembl_gene_id":"ENSG00000169629.11","gene_symbol":"RGPD8","gene_name":"RANBP2-like and GRIP domain containing 8 [Source:HGNC Symbol;Acc:HGNC:9849]","synonyms":"RANBP2L1,RanBP2alpha","biotype":"protein_coding","ncbi_id":"727851","summary":null,"start":112370092,"end":112434488,"strand":-1,"description":"RANBP2-like and GRIP domain containing 8 [Source:HGNC Symbol;Acc:HGNC:9849]"}, {"versioned_ensembl_gene_id":"ENSG00000235995.1","gene_symbol":"UBE2V1P6","gene_name":"ubiquitin conjugating enzyme E2 V1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44889]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287279","summary":null,"start":169115195,"end":169115680,"strand":1,"description":"ubiquitin conjugating enzyme E2 V1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44889]"}, {"versioned_ensembl_gene_id":"ENSG00000180921.6","gene_symbol":"FAM83H","gene_name":"family with sequence similarity 83 member H [Source:HGNC Symbol;Acc:HGNC:24797]","synonyms":"FLJ46072","biotype":"protein_coding","ncbi_id":"286077","summary":"The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010]","start":143723933,"end":143733801,"strand":-1,"description":"family with sequence similarity 83 member H [Source:HGNC Symbol;Acc:HGNC:24797]"}, {"versioned_ensembl_gene_id":"ENSG00000225327.3","gene_symbol":"USP17L3","gene_name":"ubiquitin specific peptidase 17-like family member 3 [Source:HGNC Symbol;Acc:HGNC:37175]","synonyms":"USP17F,USP17B","biotype":"protein_coding","ncbi_id":"645836","summary":null,"start":7976393,"end":7977985,"strand":-1,"description":"ubiquitin specific peptidase 17-like family member 3 [Source:HGNC Symbol;Acc:HGNC:37175]"}, {"versioned_ensembl_gene_id":"ENSG00000225725.4","gene_symbol":"FAM66E","gene_name":"family with sequence similarity 66 member E [Source:HGNC Symbol;Acc:HGNC:18735]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100132103","summary":null,"start":7955014,"end":8008755,"strand":1,"description":"family with sequence similarity 66 member E [Source:HGNC Symbol;Acc:HGNC:18735]"}, {"versioned_ensembl_gene_id":"ENSG00000227751.1","gene_symbol":"AC004824.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17406760,"end":17407382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226066.1","gene_symbol":"AC009541.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":136485656,"end":136488317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179051.13","gene_symbol":"RCC2","gene_name":"regulator of chromosome condensation 2 [Source:HGNC Symbol;Acc:HGNC:30297]","synonyms":"TD-60","biotype":"protein_coding","ncbi_id":"55920","summary":"The protein encoded by this gene is a guanine exchange factor that is active on RalA, a small GTPase. The encoded protein and RalA are both essential for proper kinetochore-microtubule function in early mitosis. This protein has been shown to be a biomarker for colorectal cancer. [provided by RefSeq, Oct 2016]","start":17406760,"end":17439724,"strand":-1,"description":"regulator of chromosome condensation 2 [Source:HGNC Symbol;Acc:HGNC:30297]"}, {"versioned_ensembl_gene_id":"ENSG00000172461.10","gene_symbol":"FUT9","gene_name":"fucosyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:4020]","synonyms":"Fuc-TIX","biotype":"protein_coding","ncbi_id":"10690","summary":"The protein encoded by this gene belongs to the glycosyltransferase family. It is localized to the golgi, and catalyzes the last step in the biosynthesis of Lewis X (LeX) antigen, the addition of a fucose to precursor polysaccharides. This protein is one of the few fucosyltransferases that synthesizes the LeX oligosaccharide (CD15) expressed in the organ buds progressing in mesenchyma during embryogenesis. It is also responsible for the expression of CD15 in mature granulocytes. A common haplotype of this gene has also been associated with susceptibility to placental malaria infection. [provided by RefSeq, Nov 2011]","start":96015984,"end":96215612,"strand":1,"description":"fucosyltransferase 9 [Source:HGNC Symbol;Acc:HGNC:4020]"}, {"versioned_ensembl_gene_id":"ENSG00000279177.1","gene_symbol":"FP236241.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7626344,"end":7627528,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255211.1","gene_symbol":"AC130365.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":7967344,"end":7968544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237038.5","gene_symbol":"USP17L8","gene_name":"ubiquitin specific peptidase 17-like family member 8 [Source:HGNC Symbol;Acc:HGNC:37181]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392188","summary":null,"start":7971661,"end":7973253,"strand":-1,"description":"ubiquitin specific peptidase 17-like family member 8 [Source:HGNC Symbol;Acc:HGNC:37181]"}, {"versioned_ensembl_gene_id":"ENSG00000259609.1","gene_symbol":"AC027807.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":84053113,"end":84080097,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205989.1","gene_symbol":"DEFB109C","gene_name":"defensin beta 109C [Source:HGNC Symbol;Acc:HGNC:43844]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100286963","summary":null,"start":7990415,"end":7997521,"strand":-1,"description":"defensin beta 109C [Source:HGNC Symbol;Acc:HGNC:43844]"}, {"versioned_ensembl_gene_id":"ENSG00000230658.1","gene_symbol":"KLHL7-AS1","gene_name":"KLHL7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43431]","synonyms":"PLATAK","biotype":"lincRNA","ncbi_id":"100775104","summary":null,"start":23101228,"end":23105703,"strand":-1,"description":"KLHL7 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:43431]"}, {"versioned_ensembl_gene_id":"ENSG00000223657.2","gene_symbol":"KRT8P51","gene_name":"keratin 8 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48883]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480676","summary":null,"start":136938280,"end":136938553,"strand":-1,"description":"keratin 8 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48883]"}, {"versioned_ensembl_gene_id":"ENSG00000275572.1","gene_symbol":"GRIFIN","gene_name":"galectin-related inter-fiber protein [Source:HGNC Symbol;Acc:HGNC:4577]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402635","summary":null,"start":2474844,"end":2476894,"strand":-1,"description":"galectin-related inter-fiber protein [Source:HGNC Symbol;Acc:HGNC:4577]"}, {"versioned_ensembl_gene_id":"ENSG00000259404.5","gene_symbol":"EFTUD1P1","gene_name":"elongation factor Tu GTP binding domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31739]","synonyms":"FAM42B,HsT19321","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"648809","summary":null,"start":84080168,"end":84126604,"strand":1,"description":"elongation factor Tu GTP binding domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31739]"}, {"versioned_ensembl_gene_id":"ENSG00000181072.11","gene_symbol":"CHRM2","gene_name":"cholinergic receptor muscarinic 2 [Source:HGNC Symbol;Acc:HGNC:1951]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1129","summary":"The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine to these receptors and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The muscarinic cholinergic receptor 2 is involved in mediation of bradycardia and a decrease in cardiac contractility. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Jul 2008]","start":136868669,"end":137020255,"strand":1,"description":"cholinergic receptor muscarinic 2 [Source:HGNC Symbol;Acc:HGNC:1951]"}, {"versioned_ensembl_gene_id":"ENSG00000116017.10","gene_symbol":"ARID3A","gene_name":"AT-rich interaction domain 3A [Source:HGNC Symbol;Acc:HGNC:3031]","synonyms":"DRIL1,BRIGHT","biotype":"protein_coding","ncbi_id":"1820","summary":"This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA binding proteins. It was found by homology to the Drosophila dead ringer gene, which is important for normal embryogenesis. Other ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation, and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]","start":925781,"end":975934,"strand":1,"description":"AT-rich interaction domain 3A [Source:HGNC Symbol;Acc:HGNC:3031]"}, {"versioned_ensembl_gene_id":"ENSG00000055332.16","gene_symbol":"EIF2AK2","gene_name":"eukaryotic translation initiation factor 2 alpha kinase 2 [Source:HGNC Symbol;Acc:HGNC:9437]","synonyms":"PRKR,PPP1R83,PKR,EIF2AK1","biotype":"protein_coding","ncbi_id":"5610","summary":"The protein encoded by this gene is a serine/threonine protein kinase that is activated by autophosphorylation after binding to dsRNA. The activated form of the encoded protein can phosphorylate translation initiation factor EIF2S1, which in turn inhibits protein synthesis. This protein is also activated by manganese ions and heparin. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":37099210,"end":37157065,"strand":-1,"description":"eukaryotic translation initiation factor 2 alpha kinase 2 [Source:HGNC Symbol;Acc:HGNC:9437]"}, {"versioned_ensembl_gene_id":"ENSG00000086232.12","gene_symbol":"EIF2AK1","gene_name":"eukaryotic translation initiation factor 2 alpha kinase 1 [Source:HGNC Symbol;Acc:HGNC:24921]","synonyms":"KIAA1369,HRI","biotype":"protein_coding","ncbi_id":"27102","summary":"The protein encoded by this gene acts at the level of translation initiation to downregulate protein synthesis in response to stress. The encoded protein is a kinase that can be inactivated by hemin. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]","start":6022244,"end":6059230,"strand":-1,"description":"eukaryotic translation initiation factor 2 alpha kinase 1 [Source:HGNC Symbol;Acc:HGNC:24921]"}, {"versioned_ensembl_gene_id":"ENSG00000229491.5","gene_symbol":"AC136489.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45183251,"end":45333917,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280807.2","gene_symbol":"TUBGCP5","gene_name":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]","synonyms":"KIAA1899,GCP5","biotype":"protein_coding","ncbi_id":"114791","summary":null,"start":23036897,"end":23039673,"strand":-1,"description":"tubulin gamma complex associated protein 5 [Source:HGNC Symbol;Acc:HGNC:18600]"}, {"versioned_ensembl_gene_id":"ENSG00000277991.4","gene_symbol":"FP236241.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7669397,"end":7681742,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165066.12","gene_symbol":"NKX6-3","gene_name":"NK6 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:26328]","synonyms":"FLJ25169","biotype":"protein_coding","ncbi_id":"157848","summary":"The NKX family of homeodomain proteins controls numerous developmental processes. Members of the NKX6 subfamily, including NKX6-3, are involved in development of the central nervous system (CNS), gastrointestinal tract, and pancreas (Alanentalo et al., 2006 [PubMed 16326147]).[supplied by OMIM, Mar 2008]","start":41645178,"end":41650669,"strand":-1,"description":"NK6 homeobox 3 [Source:HGNC Symbol;Acc:HGNC:26328]"}, {"versioned_ensembl_gene_id":"ENSG00000215301.9","gene_symbol":"DDX3X","gene_name":"DEAD-box helicase 3, X-linked [Source:HGNC Symbol;Acc:HGNC:2745]","synonyms":"HLP2,DDX3,DDX14,DBX","biotype":"protein_coding","ncbi_id":"1654","summary":"The protein encoded by this gene is a member of the large DEAD-box protein family, that is defined by the presence of the conserved Asp-Glu-Ala-Asp (DEAD) motif, and has ATP-dependent RNA helicase activity. This protein has been reported to display a high level of RNA-independent ATPase activity, and unlike most DEAD-box helicases, the ATPase activity is thought to be stimulated by both RNA and DNA. This protein has multiple conserved domains and is thought to play roles in both the nucleus and cytoplasm. Nuclear roles include transcriptional regulation, mRNP assembly, pre-mRNA splicing, and mRNA export. In the cytoplasm, this protein is thought to be involved in translation, cellular signaling, and viral replication. Misregulation of this gene has been implicated in tumorigenesis. This gene has a paralog located in the nonrecombining region of the Y chromosome. Pseudogenes sharing similarity to both this gene and the DDX3Y paralog are found on chromosome 4 and the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":41333348,"end":41364472,"strand":1,"description":"DEAD-box helicase 3, X-linked [Source:HGNC Symbol;Acc:HGNC:2745]"}, {"versioned_ensembl_gene_id":"ENSG00000261041.1","gene_symbol":"AC138749.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28545912,"end":28549777,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254973.1","gene_symbol":"AC105219.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143758153,"end":143771822,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140259.6","gene_symbol":"MFAP1","gene_name":"microfibril associated protein 1 [Source:HGNC Symbol;Acc:HGNC:7032]","synonyms":"AMP","biotype":"protein_coding","ncbi_id":"4236","summary":null,"start":43804492,"end":43824802,"strand":-1,"description":"microfibril associated protein 1 [Source:HGNC Symbol;Acc:HGNC:7032]"}, {"versioned_ensembl_gene_id":"ENSG00000276849.6","gene_symbol":"TRBC2","gene_name":"T-cell receptor beta constant 2 [Source:HGNC Symbol;Acc:HGNC:12157]","synonyms":"TCRBC2","biotype":"TR_C_gene","ncbi_id":"28638","summary":null,"start":142862134,"end":142863838,"strand":1,"description":"T-cell receptor beta constant 2 [Source:HGNC Symbol;Acc:HGNC:12157]"}, {"versioned_ensembl_gene_id":"ENSG00000227717.4","gene_symbol":"AC138749.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28553638,"end":28561379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260444.1","gene_symbol":"AC138749.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28564986,"end":28565152,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280540.1","gene_symbol":"LINC01480","gene_name":"long intergenic non-protein coding RNA 1480 [Source:HGNC Symbol;Acc:HGNC:51124]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927931","summary":null,"start":41543524,"end":41545246,"strand":1,"description":"long intergenic non-protein coding RNA 1480 [Source:HGNC Symbol;Acc:HGNC:51124]"}, {"versioned_ensembl_gene_id":"ENSG00000237401.6","gene_symbol":"LINC01304","gene_name":"long intergenic non-protein coding RNA 1304 [Source:HGNC Symbol;Acc:HGNC:50472]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505964","summary":null,"start":3957655,"end":3974070,"strand":-1,"description":"long intergenic non-protein coding RNA 1304 [Source:HGNC Symbol;Acc:HGNC:50472]"}, {"versioned_ensembl_gene_id":"ENSG00000261581.1","gene_symbol":"HERC2P11","gene_name":"hect domain and RLD 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49882]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100996738","summary":null,"start":28575019,"end":28579400,"strand":-1,"description":"hect domain and RLD 2 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49882]"}, {"versioned_ensembl_gene_id":"ENSG00000167046.4","gene_symbol":"AL357033.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62640719,"end":62643304,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228308.1","gene_symbol":"LINC01209","gene_name":"long intergenic non-protein coding RNA 1209 [Source:HGNC Symbol;Acc:HGNC:49640]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928684","summary":null,"start":176814155,"end":176817001,"strand":-1,"description":"long intergenic non-protein coding RNA 1209 [Source:HGNC Symbol;Acc:HGNC:49640]"}, {"versioned_ensembl_gene_id":"ENSG00000232461.1","gene_symbol":"AC092920.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":176643941,"end":176867838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139192.11","gene_symbol":"TAPBPL","gene_name":"TAP binding protein like [Source:HGNC Symbol;Acc:HGNC:30683]","synonyms":"TAPBPR,TAPBP-R,FLJ10143","biotype":"protein_coding","ncbi_id":"55080","summary":"Tapasin, or TAPBP (MIM 601962), is a member of the variable-constant Ig superfamily that links major histocompatibility complex (MHC) class I molecules to the transporter associated with antigen processing (TAP; see MIM 170260) in the endoplasmic reticulum (ER). The TAPBP gene is located near the MHC complex on chromosome 6p21.3. TAPBPL is a member of the Ig superfamily that is localized on chromosome 12p13.3, a region somewhat paralogous to the MHC.[supplied by OMIM, Mar 2008]","start":6451690,"end":6466517,"strand":1,"description":"TAP binding protein like [Source:HGNC Symbol;Acc:HGNC:30683]"}, {"versioned_ensembl_gene_id":"ENSG00000124688.13","gene_symbol":"MAD2L1BP","gene_name":"MAD2L1 binding protein [Source:HGNC Symbol;Acc:HGNC:21059]","synonyms":"KIAA0110,dJ261G23.1,CMT2","biotype":"protein_coding","ncbi_id":"9587","summary":"The protein encoded by this gene was identified as a binding protein of the MAD2 mitotic arrest deficient-like 1 (MAD2/MAD2L1). MAD2 is a key component of the spindle checkpoint that delays the onset of anaphase until all the kinetochores are attached to the spindle. This protein may interact with the spindle checkpoint and coordinate cell cycle events in late mitosis. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":43629540,"end":43640952,"strand":1,"description":"MAD2L1 binding protein [Source:HGNC Symbol;Acc:HGNC:21059]"}, {"versioned_ensembl_gene_id":"ENSG00000277277.3","gene_symbol":"CU633980.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7768884,"end":7770591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232437.1","gene_symbol":"RPS26P42","gene_name":"ribosomal protein S26 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271568","summary":null,"start":75125217,"end":75125862,"strand":1,"description":"ribosomal protein S26 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:36243]"}, {"versioned_ensembl_gene_id":"ENSG00000275162.1","gene_symbol":"AC005391.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":956485,"end":958149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267159.2","gene_symbol":"AC005379.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":928259,"end":928817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273590.4","gene_symbol":"SMIM11B","gene_name":"small integral membrane protein 11B [Source:HGNC Symbol;Acc:HGNC:51846]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723553","summary":null,"start":7744962,"end":7777853,"strand":1,"description":"small integral membrane protein 11B [Source:HGNC Symbol;Acc:HGNC:51846]"}, {"versioned_ensembl_gene_id":"ENSG00000260459.2","gene_symbol":"FTLP14","gene_name":"ferritin light chain pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37964]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100462794","summary":null,"start":68822587,"end":68823070,"strand":1,"description":"ferritin light chain pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:37964]"}, {"versioned_ensembl_gene_id":"ENSG00000156671.12","gene_symbol":"SAMD8","gene_name":"sterile alpha motif domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26320]","synonyms":"SMSr,FLJ25082","biotype":"protein_coding","ncbi_id":"142891","summary":null,"start":75099586,"end":75182123,"strand":1,"description":"sterile alpha motif domain containing 8 [Source:HGNC Symbol;Acc:HGNC:26320]"}, {"versioned_ensembl_gene_id":"ENSG00000240006.1","gene_symbol":"LINC02004","gene_name":"long intergenic non-protein coding RNA 2004 [Source:HGNC Symbol;Acc:HGNC:52838]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374119","summary":null,"start":134313576,"end":134321171,"strand":1,"description":"long intergenic non-protein coding RNA 2004 [Source:HGNC Symbol;Acc:HGNC:52838]"}, {"versioned_ensembl_gene_id":"ENSG00000260798.1","gene_symbol":"AC099314.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":68814330,"end":68823526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231244.1","gene_symbol":"PSMC1P3","gene_name":"proteasome 26S subunit, ATPase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39778]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392100","summary":null,"start":136713871,"end":136715188,"strand":1,"description":"proteasome 26S subunit, ATPase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39778]"}, {"versioned_ensembl_gene_id":"ENSG00000131778.18","gene_symbol":"CHD1L","gene_name":"chromodomain helicase DNA binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:1916]","synonyms":"ALC1","biotype":"protein_coding","ncbi_id":"9557","summary":"This gene encodes a DNA helicase protein involved in DNA repair. The protein converts ATP to add poly(ADP-ribose) as it regulates chromatin relaxation following DNA damage. Overexpression of this gene has been linked to several types of cancers. [provided by RefSeq, Feb 2017]","start":147242641,"end":147295766,"strand":1,"description":"chromodomain helicase DNA binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:1916]"}, {"versioned_ensembl_gene_id":"ENSG00000106631.8","gene_symbol":"MYL7","gene_name":"myosin light chain 7 [Source:HGNC Symbol;Acc:HGNC:21719]","synonyms":"MYLC2A,MYL2A","biotype":"protein_coding","ncbi_id":"58498","summary":null,"start":44138864,"end":44141332,"strand":-1,"description":"myosin light chain 7 [Source:HGNC Symbol;Acc:HGNC:21719]"}, {"versioned_ensembl_gene_id":"ENSG00000039068.18","gene_symbol":"CDH1","gene_name":"cadherin 1 [Source:HGNC Symbol;Acc:HGNC:1748]","synonyms":"uvomorulin,UVO,CD324","biotype":"protein_coding","ncbi_id":"999","summary":"This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Mutations in this gene are correlated with gastric, breast, colorectal, thyroid and ovarian cancer. Loss of function of this gene is thought to contribute to cancer progression by increasing proliferation, invasion, and/or metastasis. The ectodomain of this protein mediates bacterial adhesion to mammalian cells and the cytoplasmic domain is required for internalization. This gene is present in a gene cluster with other members of the cadherin family on chromosome 16. [provided by RefSeq, Nov 2015]","start":68737225,"end":68835548,"strand":1,"description":"cadherin 1 [Source:HGNC Symbol;Acc:HGNC:1748]"}, {"versioned_ensembl_gene_id":"ENSG00000234352.9","gene_symbol":"AC009264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":136685559,"end":137182107,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272443.1","gene_symbol":"OR13Z2P","gene_name":"olfactory receptor family 13 subfamily Z member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31241]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403229","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":147445579,"end":147446133,"strand":1,"description":"olfactory receptor family 13 subfamily Z member 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:31241]"}, {"versioned_ensembl_gene_id":"ENSG00000226653.2","gene_symbol":"OR13Z1P","gene_name":"olfactory receptor family 13 subfamily Z member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31240]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"403228","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":147419050,"end":147419883,"strand":1,"description":"olfactory receptor family 13 subfamily Z member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:31240]"}, {"versioned_ensembl_gene_id":"ENSG00000273071.1","gene_symbol":"AC242426.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":147173186,"end":147252659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067048.16","gene_symbol":"DDX3Y","gene_name":"DEAD-box helicase 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:2699]","synonyms":"DBY","biotype":"protein_coding","ncbi_id":"8653","summary":"The protein encoded by this gene is a member of the DEAD-box RNA helicase family, characterized by nine conserved motifs, included the conserved Asp-Glu-Ala-Asp (DEAD) motif. These motifs are thought to be involved in ATP binding, hydrolysis, RNA binding, and in the formation of intramolecular interactions. This protein shares high similarity to DDX3X, on the X chromosome, but a deletion of this gene is not complemented by DDX3X. Mutations in this gene result in male infertility, a reduction in germ cell numbers, and can result in Sertoli-cell only sydrome. Pseudogenes sharing similarity to both this gene and the DDX3X paralog are found on chromosome 4 and the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]","start":12904108,"end":12920478,"strand":1,"description":"DEAD-box helicase 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:2699]"}, {"versioned_ensembl_gene_id":"ENSG00000272480.1","gene_symbol":"AC242628.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":147482238,"end":147482628,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258303.1","gene_symbol":"AC012464.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":93836167,"end":93838038,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236806.1","gene_symbol":"AC242426.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147223554,"end":147224348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258274.1","gene_symbol":"AC012085.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93707791,"end":93737823,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224469.1","gene_symbol":"AC009517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137164043,"end":137164612,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231888.1","gene_symbol":"MTND5P15","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42277]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873259","summary":null,"start":177010719,"end":177011067,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:42277]"}, {"versioned_ensembl_gene_id":"ENSG00000117308.14","gene_symbol":"GALE","gene_name":"UDP-galactose-4-epimerase [Source:HGNC Symbol;Acc:HGNC:4116]","synonyms":"SDR1E1","biotype":"protein_coding","ncbi_id":"2582","summary":"This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and cognitive disability, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). Multiple alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Jul 2008]","start":23795599,"end":23800804,"strand":-1,"description":"UDP-galactose-4-epimerase [Source:HGNC Symbol;Acc:HGNC:4116]"}, {"versioned_ensembl_gene_id":"ENSG00000235015.1","gene_symbol":"GEMIN2P1","gene_name":"gem nuclear organelle associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929669","summary":null,"start":153717303,"end":153718347,"strand":-1,"description":"gem nuclear organelle associated protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49561]"}, {"versioned_ensembl_gene_id":"ENSG00000215032.2","gene_symbol":"GNL3LP1","gene_name":"G protein nucleolar 3 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25733]","synonyms":"GNL3LP,FLJ12595","biotype":"processed_pseudogene","ncbi_id":"80060","summary":null,"start":60891935,"end":60893577,"strand":-1,"description":"G protein nucleolar 3 like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:25733]"}, {"versioned_ensembl_gene_id":"ENSG00000169372.12","gene_symbol":"CRADD","gene_name":"CASP2 and RIPK1 domain containing adaptor with death domain [Source:HGNC Symbol;Acc:HGNC:2340]","synonyms":"RAIDD","biotype":"protein_coding","ncbi_id":"8738","summary":"This gene encodes a protein containing a death domain (DD) motif. This protein recruits caspase 2/ICH1 to the cell death signal transduction complex, which includes tumor necrosis factor receptor 1 (TNFR1A) and RIPK1/RIP kinase, and acts in promoting apoptosis. A mutation in this gene was associated with cognitive disability. A related pseudogene is found on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":93677375,"end":93894840,"strand":1,"description":"CASP2 and RIPK1 domain containing adaptor with death domain [Source:HGNC Symbol;Acc:HGNC:2340]"}, {"versioned_ensembl_gene_id":"ENSG00000269845.1","gene_symbol":"AC092364.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":21750747,"end":21753438,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197020.10","gene_symbol":"ZNF100","gene_name":"zinc finger protein 100 [Source:HGNC Symbol;Acc:HGNC:12880]","synonyms":null,"biotype":"protein_coding","ncbi_id":"163227","summary":null,"start":21722766,"end":21767628,"strand":-1,"description":"zinc finger protein 100 [Source:HGNC Symbol;Acc:HGNC:12880]"}, {"versioned_ensembl_gene_id":"ENSG00000232616.9","gene_symbol":"SKIV2L","gene_name":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]","synonyms":"SKIV2,DDX13,SKI2W,170A,SKIV2L1,HLP","biotype":"protein_coding","ncbi_id":"6499","summary":"DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008]","start":32035523,"end":32046194,"strand":1,"description":"Ski2 like RNA helicase [Source:HGNC Symbol;Acc:HGNC:10898]"}, {"versioned_ensembl_gene_id":"ENSG00000096080.11","gene_symbol":"MRPS18A","gene_name":"mitochondrial ribosomal protein S18A [Source:HGNC Symbol;Acc:HGNC:14515]","synonyms":"MRPS18-3,FLJ10548","biotype":"protein_coding","ncbi_id":"55168","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S18P family. The encoded protein is one of three that has significant sequence similarity to bacterial S18 proteins. The primary sequences of the three human mitochondrial S18 proteins are no more closely related to each other than they are to the prokaryotic S18 proteins. A pseudogene corresponding to this gene is found on chromosome 3p. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]","start":43671303,"end":43687791,"strand":-1,"description":"mitochondrial ribosomal protein S18A [Source:HGNC Symbol;Acc:HGNC:14515]"}, {"versioned_ensembl_gene_id":"ENSG00000138750.14","gene_symbol":"NUP54","gene_name":"nucleoporin 54 [Source:HGNC Symbol;Acc:HGNC:17359]","synonyms":null,"biotype":"protein_coding","ncbi_id":"53371","summary":"The nuclear envelope creates distinct nuclear and cytoplasmic compartments in eukaryotic cells. It consists of two concentric membranes perforated by nuclear pores, large protein complexes that form aqueous channels to regulate the flow of macromolecules between the nucleus and the cytoplasm. These complexes are composed of at least 100 different polypeptide subunits, many of which belong to the nucleoporin family. This gene encodes a member of the phe-gly (FG) repeat-containing nucleoporin subset. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2013]","start":76114659,"end":76148515,"strand":-1,"description":"nucleoporin 54 [Source:HGNC Symbol;Acc:HGNC:17359]"}, {"versioned_ensembl_gene_id":"ENSG00000242687.2","gene_symbol":"AC004893.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":99013165,"end":99048240,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000136717.14","gene_symbol":"BIN1","gene_name":"bridging integrator 1 [Source:HGNC Symbol;Acc:HGNC:1052]","synonyms":"SH3P9,AMPHL,AMPH2","biotype":"protein_coding","ncbi_id":"274","summary":"This gene encodes several isoforms of a nucleocytoplasmic adaptor protein, one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor. Isoforms that are expressed in the central nervous system may be involved in synaptic vesicle endocytosis and may interact with dynamin, synaptojanin, endophilin, and clathrin. Isoforms that are expressed in muscle and ubiquitously expressed isoforms localize to the cytoplasm and nucleus and activate a caspase-independent apoptotic process. Studies in mouse suggest that this gene plays an important role in cardiac muscle development. Alternate splicing of the gene results in several transcript variants encoding different isoforms. Aberrant splice variants expressed in tumor cell lines have also been described. [provided by RefSeq, Mar 2016]","start":127048027,"end":127107355,"strand":-1,"description":"bridging integrator 1 [Source:HGNC Symbol;Acc:HGNC:1052]"}, {"versioned_ensembl_gene_id":"ENSG00000238109.1","gene_symbol":"AC004893.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":98998538,"end":98999930,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198742.9","gene_symbol":"SMURF1","gene_name":"SMAD specific E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:16807]","synonyms":"KIAA1625","biotype":"protein_coding","ncbi_id":"57154","summary":"This gene encodes a ubiquitin ligase that is specific for receptor-regulated SMAD proteins in the bone morphogenetic protein (BMP) pathway. This protein plays a key roll in the regulation of cell motility, cell signalling, and cell polarity. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2010]","start":99027438,"end":99144100,"strand":-1,"description":"SMAD specific E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:16807]"}, {"versioned_ensembl_gene_id":"ENSG00000157999.5","gene_symbol":"ANKRD61","gene_name":"ankyrin repeat domain 61 [Source:HGNC Symbol;Acc:HGNC:22467]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100310846","summary":null,"start":6031376,"end":6036386,"strand":1,"description":"ankyrin repeat domain 61 [Source:HGNC Symbol;Acc:HGNC:22467]"}, {"versioned_ensembl_gene_id":"ENSG00000226992.1","gene_symbol":"AC145625.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":238788648,"end":238789716,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106305.9","gene_symbol":"AIMP2","gene_name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 2 [Source:HGNC Symbol;Acc:HGNC:20609]","synonyms":"JTV-1,PRO0992,p38,JTV1","biotype":"protein_coding","ncbi_id":"7965","summary":"The protein encoded by this gene is part of the aminoacyl-tRNA synthetase complex, which contains nine different aminoacyl-tRNA synthetases and three non-enzymatic factors. The encoded protein is one of the non-enzymatic factors and is required for assembly and stability of the complex. [provided by RefSeq, May 2016]","start":6009245,"end":6023834,"strand":1,"description":"aminoacyl tRNA synthetase complex interacting multifunctional protein 2 [Source:HGNC Symbol;Acc:HGNC:20609]"}, {"versioned_ensembl_gene_id":"ENSG00000139190.16","gene_symbol":"VAMP1","gene_name":"vesicle associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:12642]","synonyms":"VAMP-1,SYB1","biotype":"protein_coding","ncbi_id":"6843","summary":"Synapotobrevins, syntaxins, and the synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Mutations in this gene are associated with autosomal dominant spastic ataxia 1. Multiple alternative splice variants have been described, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2014]","start":6462237,"end":6470987,"strand":-1,"description":"vesicle associated membrane protein 1 [Source:HGNC Symbol;Acc:HGNC:12642]"}, {"versioned_ensembl_gene_id":"ENSG00000233608.3","gene_symbol":"TWIST2","gene_name":"twist family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:20670]","synonyms":"Dermo-1,bHLHa39,DERMO1","biotype":"protein_coding","ncbi_id":"117581","summary":"The protein encoded by this gene is a basic helix-loop-helix type transcription factor and shares similarity with Twist. This protein may inhibit osteoblast maturation and maintain cells in a preosteoblast phenotype during osteoblast development. This gene may be upregulated in certain cancers. Mutations in this gene cause focal facial dermal dysplasia 3, Setleis type. Two transcript variants encoding the same protein have been found. [provided by RefSeq, Apr 2014]","start":238848032,"end":238910543,"strand":1,"description":"twist family bHLH transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:20670]"}, {"versioned_ensembl_gene_id":"ENSG00000262294.1","gene_symbol":"AC129507.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":352638,"end":357581,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220773.1","gene_symbol":"RPSAP44","gene_name":"ribosomal protein SA pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36891]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"652411","summary":null,"start":54624605,"end":54625488,"strand":1,"description":"ribosomal protein SA pseudogene 44 [Source:HGNC Symbol;Acc:HGNC:36891]"}, {"versioned_ensembl_gene_id":"ENSG00000249411.1","gene_symbol":"AC022325.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175017016,"end":175019214,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220635.2","gene_symbol":"KRASP1","gene_name":"KRAS proto-oncogene, GTPase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6406]","synonyms":"KRAS1P","biotype":"processed_pseudogene","ncbi_id":"3844","summary":null,"start":54770583,"end":54771134,"strand":1,"description":"KRAS proto-oncogene, GTPase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6406]"}, {"versioned_ensembl_gene_id":"ENSG00000249284.1","gene_symbol":"AC095050.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175286605,"end":175290767,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224984.1","gene_symbol":"AL512363.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":54840118,"end":54840855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262119.1","gene_symbol":"AL079343.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":26592747,"end":26594517,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276848.4","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"FLJ00060,LENG12","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54464632,"end":54477600,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000139910.19","gene_symbol":"NOVA1","gene_name":"NOVA alternative splicing regulator 1 [Source:HGNC Symbol;Acc:HGNC:7886]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4857","summary":"This gene encodes a neuron-specific RNA-binding protein, a member of the Nova family of paraneoplastic disease antigens, that is recognized and inhibited by paraneoplastic antibodies. These antibodies are found in the sera of patients with paraneoplastic opsoclonus-ataxia, breast cancer, and small cell lung cancer. Alternatively spliced transcripts encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":26443093,"end":26597754,"strand":-1,"description":"NOVA alternative splicing regulator 1 [Source:HGNC Symbol;Acc:HGNC:7886]"}, {"versioned_ensembl_gene_id":"ENSG00000226161.1","gene_symbol":"EIF4A1P5","gene_name":"eukaryotic translation initiation factor 4A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37924]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"390394","summary":null,"start":36938400,"end":36939494,"strand":-1,"description":"eukaryotic translation initiation factor 4A1 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37924]"}, {"versioned_ensembl_gene_id":"ENSG00000270028.1","gene_symbol":"AC079315.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":123925461,"end":123926083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000119242.8","gene_symbol":"CCDC92","gene_name":"coiled-coil domain containing 92 [Source:HGNC Symbol;Acc:HGNC:29563]","synonyms":"FLJ22471","biotype":"protein_coding","ncbi_id":"80212","summary":null,"start":123918660,"end":123972831,"strand":-1,"description":"coiled-coil domain containing 92 [Source:HGNC Symbol;Acc:HGNC:29563]"}, {"versioned_ensembl_gene_id":"ENSG00000177409.11","gene_symbol":"SAMD9L","gene_name":"sterile alpha motif domain containing 9 like [Source:HGNC Symbol;Acc:HGNC:1349]","synonyms":"KIAA2005,FLJ39885,C7orf6","biotype":"protein_coding","ncbi_id":"219285","summary":"This gene encodes a cytoplasmic protein that acts as a tumor suppressor but also plays a key role in cell proliferation and the innate immune response to viral infection. The encoded protein contains an N-terminal sterile alpha motif domain. Naturally occurring mutations in this gene are associated with myeloid disorders such as juvenile myelomonocytic leukemia, acute myeloid leukemia, and myelodysplastic syndrome. Naturally occurring mutations are also associated with hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome. [provided by RefSeq, Apr 2017]","start":93130055,"end":93148369,"strand":-1,"description":"sterile alpha motif domain containing 9 like [Source:HGNC Symbol;Acc:HGNC:1349]"}, {"versioned_ensembl_gene_id":"ENSG00000248551.1","gene_symbol":"AC095050.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175346358,"end":175403110,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138316.10","gene_symbol":"ADAMTS14","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 14 [Source:HGNC Symbol;Acc:HGNC:14899]","synonyms":null,"biotype":"protein_coding","ncbi_id":"140766","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme cleaves amino-terminal propeptides from type I procollagen, a necessary step in the formation of collagen fibers. Mutations in this gene may be associated with osteoarthritis in human patients. [provided by RefSeq, May 2016]","start":70672803,"end":70762441,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 14 [Source:HGNC Symbol;Acc:HGNC:14899]"}, {"versioned_ensembl_gene_id":"ENSG00000102174.8","gene_symbol":"PHEX","gene_name":"phosphate regulating endopeptidase homolog X-linked [Source:HGNC Symbol;Acc:HGNC:8918]","synonyms":"XLH,PEX,HYP1,HYP,HPDR1,HPDR","biotype":"protein_coding","ncbi_id":"5251","summary":"The protein encoded by this gene is a transmembrane endopeptidase that belongs to the type II integral membrane zinc-dependent endopeptidase family. The protein is thought to be involved in bone and dentin mineralization and renal phosphate reabsorption. Mutations in this gene cause X-linked hypophosphatemic rickets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":22032441,"end":22251310,"strand":1,"description":"phosphate regulating endopeptidase homolog X-linked [Source:HGNC Symbol;Acc:HGNC:8918]"}, {"versioned_ensembl_gene_id":"ENSG00000276829.1","gene_symbol":"AC016911.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22861112,"end":22861834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197302.10","gene_symbol":"ZNF720","gene_name":"zinc finger protein 720 [Source:HGNC Symbol;Acc:HGNC:26987]","synonyms":null,"biotype":"protein_coding","ncbi_id":"124411","summary":null,"start":31713229,"end":31794869,"strand":1,"description":"zinc finger protein 720 [Source:HGNC Symbol;Acc:HGNC:26987]"}, {"versioned_ensembl_gene_id":"ENSG00000269938.1","gene_symbol":"AC068790.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123968023,"end":123968579,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273291.5","gene_symbol":"AC092042.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42809446,"end":43055871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260633.1","gene_symbol":"AC010207.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":134347288,"end":134349233,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270130.1","gene_symbol":"AC068790.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123960717,"end":123961244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260072.1","gene_symbol":"AC008938.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":24472798,"end":24495177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215734.3","gene_symbol":"MRPL20P1","gene_name":"mitochondrial ribosomal protein L20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29699]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359737","summary":null,"start":36994643,"end":36995075,"strand":1,"description":"mitochondrial ribosomal protein L20 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:29699]"}, {"versioned_ensembl_gene_id":"ENSG00000256596.1","gene_symbol":"AC026358.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124206228,"end":124209018,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265182.1","gene_symbol":"AC100778.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":49495147,"end":49496896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250091.2","gene_symbol":"DNAH10OS","gene_name":"dynein axonemal heavy chain 10 opposite strand [Source:HGNC Symbol;Acc:HGNC:37121]","synonyms":"FLJ45278","biotype":"protein_coding","ncbi_id":"642797","summary":null,"start":123926424,"end":123934984,"strand":-1,"description":"dynein axonemal heavy chain 10 opposite strand [Source:HGNC Symbol;Acc:HGNC:37121]"}, {"versioned_ensembl_gene_id":"ENSG00000172426.15","gene_symbol":"RSPH9","gene_name":"radial spoke head 9 homolog [Source:HGNC Symbol;Acc:HGNC:21057]","synonyms":"CILD12,C6orf206,MRPS18AL1,FLJ30845","biotype":"protein_coding","ncbi_id":"221421","summary":"This gene encodes a protein thought to be a component of the radial spoke head in motile cilia and flagella. Mutations in this gene are associated with primary ciliary dyskinesia 12. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]","start":43645046,"end":43672599,"strand":1,"description":"radial spoke head 9 homolog [Source:HGNC Symbol;Acc:HGNC:21057]"}, {"versioned_ensembl_gene_id":"ENSG00000269997.1","gene_symbol":"AC068790.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123966077,"end":123966629,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256827.1","gene_symbol":"AC068790.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":124005871,"end":124006225,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270061.1","gene_symbol":"AC068790.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123969990,"end":123970344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179195.15","gene_symbol":"ZNF664","gene_name":"zinc finger protein 664 [Source:HGNC Symbol;Acc:HGNC:25406]","synonyms":"ZFOC1,DKFZp761B128,ZNF176","biotype":"protein_coding","ncbi_id":"144348","summary":null,"start":123971845,"end":124015439,"strand":1,"description":"zinc finger protein 664 [Source:HGNC Symbol;Acc:HGNC:25406]"}, {"versioned_ensembl_gene_id":"ENSG00000232518.3","gene_symbol":"AC074366.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38668202,"end":38671421,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269899.1","gene_symbol":"AC025857.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":11846154,"end":11846391,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269136.1","gene_symbol":"BRI3BPP1","gene_name":"BRI3 binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51482]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129976","summary":null,"start":21800480,"end":21801266,"strand":1,"description":"BRI3 binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51482]"}, {"versioned_ensembl_gene_id":"ENSG00000143891.16","gene_symbol":"GALM","gene_name":"galactose mutarotase [Source:HGNC Symbol;Acc:HGNC:24063]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130589","summary":"This gene encodes an enzyme that catalyzes the epimerization of hexose sugars such as glucose and galactose. The encoded protein is expressed in the cytoplasm and has a preference for galactose. The encoded protein may be required for normal galactose metabolism by maintaining the equilibrium of alpha and beta anomers of galactose.[provided by RefSeq, Mar 2009]","start":38665910,"end":38741237,"strand":1,"description":"galactose mutarotase [Source:HGNC Symbol;Acc:HGNC:24063]"}, {"versioned_ensembl_gene_id":"ENSG00000164733.20","gene_symbol":"CTSB","gene_name":"cathepsin B [Source:HGNC Symbol;Acc:HGNC:2527]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1508","summary":"This gene encodes a member of the C1 family of peptidases. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate multiple protein products. These products include the cathepsin B light and heavy chains, which can dimerize to form the double chain form of the enzyme. This enzyme is a lysosomal cysteine protease with both endopeptidase and exopeptidase activity that may play a role in protein turnover. It is also known as amyloid precursor protein secretase and is involved in the proteolytic processing of amyloid precursor protein (APP). Incomplete proteolytic processing of APP has been suggested to be a causative factor in Alzheimer's disease, the most common cause of dementia. Overexpression of the encoded protein has been associated with esophageal adenocarcinoma and other tumors. Both Cathepsin B and Cathepsin L are involved in the cleavage of the spike protein from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) upon its entry to the human host cell. Multiple pseudogenes of this gene have been identified. [provided by RefSeq, Sep 2020]","start":11842524,"end":11869448,"strand":-1,"description":"cathepsin B [Source:HGNC Symbol;Acc:HGNC:2527]"}, {"versioned_ensembl_gene_id":"ENSG00000206552.4","gene_symbol":"KRBOX1-AS1","gene_name":"KRBOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42942]","synonyms":"FLJ32776","biotype":"antisense_RNA","ncbi_id":"100506275","summary":null,"start":42934252,"end":42936785,"strand":-1,"description":"KRBOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42942]"}, {"versioned_ensembl_gene_id":"ENSG00000280571.1","gene_symbol":"AC099329.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42757177,"end":42804518,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114019.14","gene_symbol":"AMOTL2","gene_name":"angiomotin like 2 [Source:HGNC Symbol;Acc:HGNC:17812]","synonyms":"LCCP","biotype":"protein_coding","ncbi_id":"51421","summary":"Angiomotin is a protein that binds angiostatin, a circulating inhibitor of the formation of new blood vessels (angiogenesis). Angiomotin mediates angiostatin inhibition of endothelial cell migration and tube formation in vitro. The protein encoded by this gene is related to angiomotin and is a member of the motin protein family. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":134355874,"end":134375479,"strand":-1,"description":"angiomotin like 2 [Source:HGNC Symbol;Acc:HGNC:17812]"}, {"versioned_ensembl_gene_id":"ENSG00000232375.1","gene_symbol":"AC092042.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":43037121,"end":43037451,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180432.5","gene_symbol":"CYP8B1","gene_name":"cytochrome P450 family 8 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2653]","synonyms":"CYP12","biotype":"protein_coding","ncbi_id":"1582","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the conversion of 7 alpha-hydroxy-4-cholesten-3-one into 7-alpha,12-alpha-dihydroxy-4-cholesten-3-one. The balance between these two steroids determines the relative amounts of cholic acid and chenodeoxycholic acid both of which are secreted in the bile and affect the solubility of cholesterol. This gene is unique among the cytochrome P450 genes in that it is intronless. [provided by RefSeq, Jul 2008]","start":42856005,"end":42876165,"strand":-1,"description":"cytochrome P450 family 8 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2653]"}, {"versioned_ensembl_gene_id":"ENSG00000276061.4","gene_symbol":"NDUFA3","gene_name":"NADH:ubiquinone oxidoreductase subunit A3 [Source:HGNC Symbol;Acc:HGNC:7686]","synonyms":"B9","biotype":"protein_coding","ncbi_id":"4696","summary":null,"start":54102782,"end":54108779,"strand":1,"description":"NADH:ubiquinone oxidoreductase subunit A3 [Source:HGNC Symbol;Acc:HGNC:7686]"}, {"versioned_ensembl_gene_id":"ENSG00000232285.1","gene_symbol":"ELOBP3","gene_name":"elongin B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39721]","synonyms":"TCEB2P3","biotype":"processed_pseudogene","ncbi_id":"100856810","summary":null,"start":48780602,"end":48780895,"strand":1,"description":"elongin B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39721]"}, {"versioned_ensembl_gene_id":"ENSG00000235288.3","gene_symbol":"AC099329.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42785087,"end":42852428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274968.1","gene_symbol":"AC008746.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54529653,"end":54529961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282297.1","gene_symbol":"TRBV30","gene_name":"T-cell receptor beta variable 30 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12214]","synonyms":"TCRBV30S1,TCRBV20S1A1N2","biotype":"TR_V_gene","ncbi_id":"28557","summary":null,"start":142873679,"end":142874492,"strand":-1,"description":"T-cell receptor beta variable 30 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12214]"}, {"versioned_ensembl_gene_id":"ENSG00000230970.3","gene_symbol":"HHATL-AS1","gene_name":"HHATL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42439]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874044","summary":null,"start":42702653,"end":42706776,"strand":1,"description":"HHATL antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42439]"}, {"versioned_ensembl_gene_id":"ENSG00000236993.2","gene_symbol":"GAPDHP21","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37773]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389970","summary":null,"start":55667341,"end":55668350,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:37773]"}, {"versioned_ensembl_gene_id":"ENSG00000282890.1","gene_symbol":"AC009975.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48809340,"end":49419013,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173811.10","gene_symbol":"CCDC13-AS1","gene_name":"CCDC13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41142]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874114","summary":null,"start":42732575,"end":42746768,"strand":1,"description":"CCDC13 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41142]"}, {"versioned_ensembl_gene_id":"ENSG00000214602.3","gene_symbol":"CTBP2P5","gene_name":"C-terminal binding protein 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45197]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646936","summary":null,"start":48915267,"end":48916530,"strand":-1,"description":"C-terminal binding protein 2 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:45197]"}, {"versioned_ensembl_gene_id":"ENSG00000282998.1","gene_symbol":"AC009975.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49202126,"end":49451896,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170820.11","gene_symbol":"FSHR","gene_name":"follicle stimulating hormone receptor [Source:HGNC Symbol;Acc:HGNC:3969]","synonyms":"FSHRO,ODG1,LGR1","biotype":"protein_coding","ncbi_id":"2492","summary":"The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]","start":48962157,"end":49154537,"strand":-1,"description":"follicle stimulating hormone receptor [Source:HGNC Symbol;Acc:HGNC:3969]"}, {"versioned_ensembl_gene_id":"ENSG00000065320.8","gene_symbol":"NTN1","gene_name":"netrin 1 [Source:HGNC Symbol;Acc:HGNC:8029]","synonyms":"NTN1L","biotype":"protein_coding","ncbi_id":"9423","summary":"Netrin is included in a family of laminin-related secreted proteins. The function of this gene has not yet been defined; however, netrin is thought to be involved in axon guidance and cell migration during development. Mutations and loss of expression of netrin suggest that variation in netrin may be involved in cancer development. [provided by RefSeq, Jul 2008]","start":9021542,"end":9244000,"strand":1,"description":"netrin 1 [Source:HGNC Symbol;Acc:HGNC:8029]"}, {"versioned_ensembl_gene_id":"ENSG00000099203.6","gene_symbol":"TMED1","gene_name":"transmembrane p24 trafficking protein 1 [Source:HGNC Symbol;Acc:HGNC:17291]","synonyms":"IL1RL1LG,Il1rl1l,ST2L,p24gamma1,p24g1,MGC1270","biotype":"protein_coding","ncbi_id":"11018","summary":"This gene belongs to the TMED (transmembrane emp24 domain-containing) protein family, which is involved in the vesicular trafficking of proteins. The protein encoded by this gene was identified by its interaction with interleukin 1 receptor-like 1 (IL1RL1) and may play a role in innate immunity. This protein lacks any similarity to other interleukin 1 ligands. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":10832438,"end":10836318,"strand":-1,"description":"transmembrane p24 trafficking protein 1 [Source:HGNC Symbol;Acc:HGNC:17291]"}, {"versioned_ensembl_gene_id":"ENSG00000277656.3","gene_symbol":"GSTT1","gene_name":"glutathione S-transferase theta 1 [Source:HGNC Symbol;Acc:HGNC:4641]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2952","summary":"The protein encoded by this gene, glutathione S-transferase (GST) theta 1 (GSTT1), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT1 and GSTT2/GSTT2B share 55% amino acid sequence identity and may play a role in human carcinogenesis. The GSTT1 gene is haplotype-specific and is absent from 38% of the population. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":24033952,"end":24042493,"strand":-1,"description":"glutathione S-transferase theta 1 [Source:HGNC Symbol;Acc:HGNC:4641]"}, {"versioned_ensembl_gene_id":"ENSG00000244607.5","gene_symbol":"CCDC13","gene_name":"coiled-coil domain containing 13 [Source:HGNC Symbol;Acc:HGNC:26358]","synonyms":"FLJ25467","biotype":"protein_coding","ncbi_id":"152206","summary":null,"start":42692663,"end":42773253,"strand":-1,"description":"coiled-coil domain containing 13 [Source:HGNC Symbol;Acc:HGNC:26358]"}, {"versioned_ensembl_gene_id":"ENSG00000261116.1","gene_symbol":"AL049555.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":54943167,"end":54945099,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264464.1","gene_symbol":"AC091170.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49499390,"end":49501860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168143.8","gene_symbol":"FAM83B","gene_name":"family with sequence similarity 83 member B [Source:HGNC Symbol;Acc:HGNC:21357]","synonyms":"FLJ30642,C6orf143","biotype":"protein_coding","ncbi_id":"222584","summary":null,"start":54846771,"end":54942022,"strand":1,"description":"family with sequence similarity 83 member B [Source:HGNC Symbol;Acc:HGNC:21357]"}, {"versioned_ensembl_gene_id":"ENSG00000259810.2","gene_symbol":"AC002519.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":31788202,"end":31790993,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000155749.12","gene_symbol":"ALS2CR12","gene_name":"amyotrophic lateral sclerosis 2 chromosome region 12 [Source:HGNC Symbol;Acc:HGNC:14439]","synonyms":null,"biotype":"protein_coding","ncbi_id":"130540","summary":null,"start":201288271,"end":201357398,"strand":-1,"description":"amyotrophic lateral sclerosis 2 chromosome region 12 [Source:HGNC Symbol;Acc:HGNC:14439]"}, {"versioned_ensembl_gene_id":"ENSG00000104695.12","gene_symbol":"PPP2CB","gene_name":"protein phosphatase 2 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9300]","synonyms":"PP2Abeta","biotype":"protein_coding","ncbi_id":"5516","summary":"This gene encodes the phosphatase 2A catalytic subunit. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. This gene encodes a beta isoform of the catalytic subunit. [provided by RefSeq, Mar 2010]","start":30774457,"end":30814314,"strand":-1,"description":"protein phosphatase 2 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9300]"}, {"versioned_ensembl_gene_id":"ENSG00000179387.9","gene_symbol":"ELMOD2","gene_name":"ELMO domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28111]","synonyms":"MGC10084","biotype":"protein_coding","ncbi_id":"255520","summary":"This gene encodes one of six engulfment and motility (ELMO) domain-containing proteins. This gene is thought to play a role in antiviral responses. Mutations in this gene may be involved in the cause of familial idiopathic pulmonary fibrosis. [provided by RefSeq, Sep 2010]","start":140524158,"end":140553770,"strand":1,"description":"ELMO domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28111]"}, {"versioned_ensembl_gene_id":"ENSG00000152133.14","gene_symbol":"GPATCH11","gene_name":"G-patch domain containing 11 [Source:HGNC Symbol;Acc:HGNC:26768]","synonyms":"FLJ38348,CENPY,CENP-Y,CCDC75","biotype":"protein_coding","ncbi_id":"253635","summary":null,"start":37084451,"end":37099244,"strand":1,"description":"G-patch domain containing 11 [Source:HGNC Symbol;Acc:HGNC:26768]"}, {"versioned_ensembl_gene_id":"ENSG00000249945.1","gene_symbol":"AC131094.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":175458289,"end":175466697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251174.1","gene_symbol":"TSEN2P1","gene_name":"tRNA splicing endonuclease subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43965]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391718","summary":null,"start":175494614,"end":175496000,"strand":1,"description":"tRNA splicing endonuclease subunit 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43965]"}, {"versioned_ensembl_gene_id":"ENSG00000231130.1","gene_symbol":"HLA-T","gene_name":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]","synonyms":"HLA-16","biotype":"unprocessed_pseudogene","ncbi_id":"352964","summary":null,"start":29896654,"end":29897786,"strand":1,"description":"major histocompatibility complex, class I, T (pseudogene) [Source:HGNC Symbol;Acc:HGNC:23478]"}, {"versioned_ensembl_gene_id":"ENSG00000262966.2","gene_symbol":"AC005695.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9171068,"end":9179118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183386.9","gene_symbol":"FHL3","gene_name":"four and a half LIM domains 3 [Source:HGNC Symbol;Acc:HGNC:3704]","synonyms":"SLIM2","biotype":"protein_coding","ncbi_id":"2275","summary":"The protein encoded by this gene is a member of a family of proteins containing a four-and-a-half LIM domain, which is a highly conserved double zinc finger motif. The encoded protein has been shown to interact with the cancer developmental regulators SMAD2, SMAD3, and SMAD4, the skeletal muscle myogenesis protein MyoD, and the high-affinity IgE beta chain regulator MZF-1. This protein may be involved in tumor suppression, repression of MyoD expression, and repression of IgE receptor expression. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":37996770,"end":38005606,"strand":-1,"description":"four and a half LIM domains 3 [Source:HGNC Symbol;Acc:HGNC:3704]"}, {"versioned_ensembl_gene_id":"ENSG00000204632.11","gene_symbol":"HLA-G","gene_name":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3135","summary":"HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]","start":29826967,"end":29831125,"strand":1,"description":"major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]"}, {"versioned_ensembl_gene_id":"ENSG00000273816.1","gene_symbol":"AC005695.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":9244666,"end":9244897,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247624.6","gene_symbol":"CPEB2-AS1","gene_name":"CPEB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49082]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441009","summary":null,"start":14909961,"end":15002045,"strand":-1,"description":"CPEB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49082]"}, {"versioned_ensembl_gene_id":"ENSG00000241852.9","gene_symbol":"C8orf58","gene_name":"chromosome 8 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:32233]","synonyms":"FLJ34715","biotype":"protein_coding","ncbi_id":"541565","summary":null,"start":22599601,"end":22604150,"strand":1,"description":"chromosome 8 open reading frame 58 [Source:HGNC Symbol;Acc:HGNC:32233]"}, {"versioned_ensembl_gene_id":"ENSG00000166091.19","gene_symbol":"CMTM5","gene_name":"CKLF like MARVEL transmembrane domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19176]","synonyms":"FLJ37521,CKLFSF5","biotype":"protein_coding","ncbi_id":"116173","summary":"This gene encodes a member of the chemokine-like factor superfamily. This family of genes encodes multi-pass membrane proteins that are similar to both the chemokine and the transmembrane 4 superfamilies of signaling molecules. The encoded protein may exhibit tumor suppressor activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":23376808,"end":23379772,"strand":1,"description":"CKLF like MARVEL transmembrane domain containing 5 [Source:HGNC Symbol;Acc:HGNC:19176]"}, {"versioned_ensembl_gene_id":"ENSG00000224204.1","gene_symbol":"PHEX-AS1","gene_name":"PHEX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40445]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873942","summary":null,"start":22162733,"end":22172983,"strand":-1,"description":"PHEX antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40445]"}, {"versioned_ensembl_gene_id":"ENSG00000227744.4","gene_symbol":"LINC01940","gene_name":"long intergenic non-protein coding RNA 1940 [Source:HGNC Symbol;Acc:HGNC:52763]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401039","summary":null,"start":238919302,"end":238926269,"strand":-1,"description":"long intergenic non-protein coding RNA 1940 [Source:HGNC Symbol;Acc:HGNC:52763]"}, {"versioned_ensembl_gene_id":"ENSG00000281618.1","gene_symbol":"IFITM10","gene_name":"interferon induced transmembrane protein 10 [Source:HGNC Symbol;Acc:HGNC:40022]","synonyms":null,"biotype":"protein_coding","ncbi_id":"402778","summary":null,"start":1729629,"end":1732648,"strand":-1,"description":"interferon induced transmembrane protein 10 [Source:HGNC Symbol;Acc:HGNC:40022]"}, {"versioned_ensembl_gene_id":"ENSG00000268184.1","gene_symbol":"AC092364.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21768772,"end":21793860,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000088726.15","gene_symbol":"TMEM40","gene_name":"transmembrane protein 40 [Source:HGNC Symbol;Acc:HGNC:25620]","synonyms":"FLJ11036","biotype":"protein_coding","ncbi_id":"55287","summary":null,"start":12733525,"end":12769457,"strand":-1,"description":"transmembrane protein 40 [Source:HGNC Symbol;Acc:HGNC:25620]"}, {"versioned_ensembl_gene_id":"ENSG00000229363.9","gene_symbol":"NELFE","gene_name":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]","synonyms":"RDBP,D6S45,RD,RDP,NELF-E","biotype":"protein_coding","ncbi_id":"7936","summary":"The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]","start":32028530,"end":32035535,"strand":-1,"description":"negative elongation factor complex member E [Source:HGNC Symbol;Acc:HGNC:13974]"}, {"versioned_ensembl_gene_id":"ENSG00000204060.7","gene_symbol":"FOXO6","gene_name":"forkhead box O6 [Source:HGNC Symbol;Acc:HGNC:24814]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100132074","summary":null,"start":41361922,"end":41383590,"strand":1,"description":"forkhead box O6 [Source:HGNC Symbol;Acc:HGNC:24814]"}, {"versioned_ensembl_gene_id":"ENSG00000236459.1","gene_symbol":"HNRNPA1P22","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39540]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729102","summary":null,"start":42889361,"end":42890306,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39540]"}, {"versioned_ensembl_gene_id":"ENSG00000240747.7","gene_symbol":"KRBOX1","gene_name":"KRAB box domain containing 1 [Source:HGNC Symbol;Acc:HGNC:38708]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100506243","summary":null,"start":42809483,"end":42942792,"strand":1,"description":"KRAB box domain containing 1 [Source:HGNC Symbol;Acc:HGNC:38708]"}, {"versioned_ensembl_gene_id":"ENSG00000229901.1","gene_symbol":"AC093151.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41375004,"end":41375669,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275389.1","gene_symbol":"AC068790.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":124085761,"end":124088598,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000120675.5","gene_symbol":"DNAJC15","gene_name":"DnaJ heat shock protein family (Hsp40) member C15 [Source:HGNC Symbol;Acc:HGNC:20325]","synonyms":"MCJ,DNAJD1","biotype":"protein_coding","ncbi_id":"29103","summary":null,"start":43023203,"end":43114224,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member C15 [Source:HGNC Symbol;Acc:HGNC:20325]"}, {"versioned_ensembl_gene_id":"ENSG00000102710.19","gene_symbol":"SUPT20H","gene_name":"SPT20 homolog, SAGA complex component [Source:HGNC Symbol;Acc:HGNC:20596]","synonyms":"SPT20,P38IP,FAM48A,C13orf19,bA421P11.4","biotype":"protein_coding","ncbi_id":"55578","summary":null,"start":37009312,"end":37059713,"strand":-1,"description":"SPT20 homolog, SAGA complex component [Source:HGNC Symbol;Acc:HGNC:20596]"}, {"versioned_ensembl_gene_id":"ENSG00000274874.1","gene_symbol":"AC068790.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":123973944,"end":124088594,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229550.1","gene_symbol":"AC012445.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":4136644,"end":4140731,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141994.15","gene_symbol":"DUS3L","gene_name":"dihydrouridine synthase 3 like [Source:HGNC Symbol;Acc:HGNC:26920]","synonyms":"FLJ13896,DUS3","biotype":"protein_coding","ncbi_id":"56931","summary":null,"start":5784832,"end":5791238,"strand":-1,"description":"dihydrouridine synthase 3 like [Source:HGNC Symbol;Acc:HGNC:26920]"}, {"versioned_ensembl_gene_id":"ENSG00000197653.15","gene_symbol":"DNAH10","gene_name":"dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]","synonyms":"FLJ43808","biotype":"protein_coding","ncbi_id":"196385","summary":"Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH10 is an inner arm dynein heavy chain (Maiti et al., 2000 [PubMed 11175280]).[supplied by OMIM, Mar 2008]","start":123762188,"end":123936206,"strand":1,"description":"dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]"}, {"versioned_ensembl_gene_id":"ENSG00000279765.3","gene_symbol":"AC013394.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":92883413,"end":92949230,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168026.18","gene_symbol":"TTC21A","gene_name":"tetratricopeptide repeat domain 21A [Source:HGNC Symbol;Acc:HGNC:30761]","synonyms":"IFT139A,STI2","biotype":"protein_coding","ncbi_id":"199223","summary":null,"start":39107704,"end":39138903,"strand":1,"description":"tetratricopeptide repeat domain 21A [Source:HGNC Symbol;Acc:HGNC:30761]"}, {"versioned_ensembl_gene_id":"ENSG00000152894.14","gene_symbol":"PTPRK","gene_name":"protein tyrosine phosphatase, receptor type K [Source:HGNC Symbol;Acc:HGNC:9674]","synonyms":"R-PTP-kappa","biotype":"protein_coding","ncbi_id":"5796","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP mu (MAM) domain, an Ig-like domain and four fibronectin type III-like repeats. This PTP was shown to mediate homophilic intercellular interaction, possibly through the interaction with beta- and gamma-catenin at adherens junctions. Expression of this gene was found to be stimulated by TGF-beta 1, which may be important for the inhibition of keratinocyte proliferation. [provided by RefSeq, Jul 2008]","start":127968779,"end":128520674,"strand":-1,"description":"protein tyrosine phosphatase, receptor type K [Source:HGNC Symbol;Acc:HGNC:9674]"}, {"versioned_ensembl_gene_id":"ENSG00000183145.8","gene_symbol":"RIPPLY3","gene_name":"ripply transcriptional repressor 3 [Source:HGNC Symbol;Acc:HGNC:3047]","synonyms":"DSCR6","biotype":"protein_coding","ncbi_id":"53820","summary":null,"start":37006150,"end":37019659,"strand":1,"description":"ripply transcriptional repressor 3 [Source:HGNC Symbol;Acc:HGNC:3047]"}, {"versioned_ensembl_gene_id":"ENSG00000274138.1","gene_symbol":"HMGN1P12","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480725","summary":null,"start":70752955,"end":70753149,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:39356]"}, {"versioned_ensembl_gene_id":"ENSG00000273873.4","gene_symbol":"BDP1","gene_name":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]","synonyms":"HSA238520,TFIIIB150,TFC5,TAF3B1,KIAA1689,TFNR,KIAA1241,TFIIIB90","biotype":"protein_coding","ncbi_id":"55814","summary":"The product of this gene is a subunit of the TFIIIB transcription initiation complex, which recruits RNA polymerase III to target promoters in order to initiate transcription. The encoded protein localizes to concentrated aggregates in the nucleus, and is required for transcription from all three types of polymerase III promoters. It is phosphorylated by casein kinase II during mitosis, resulting in its release from chromatin and suppression of polymerase III transcription. [provided by RefSeq, Jul 2008]","start":70670918,"end":70783123,"strand":1,"description":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Symbol;Acc:HGNC:13652]"}, {"versioned_ensembl_gene_id":"ENSG00000270532.1","gene_symbol":"PEBP1P2","gene_name":"phosphatidylethanolamine binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44344]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"647307","summary":null,"start":85341281,"end":85341838,"strand":-1,"description":"phosphatidylethanolamine binding protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44344]"}, {"versioned_ensembl_gene_id":"ENSG00000079805.16","gene_symbol":"DNM2","gene_name":"dynamin 2 [Source:HGNC Symbol;Acc:HGNC:2974]","synonyms":"CMTDI1,CMT2M,DYNII,DYN2,DI-CMTB,CMTDIB","biotype":"protein_coding","ncbi_id":"1785","summary":"Dynamins represent one of the subfamilies of GTP-binding proteins. These proteins share considerable sequence similarity over the N-terminal portion of the molecule, which contains the GTPase domain. Dynamins are associated with microtubules. They have been implicated in cell processes such as endocytosis and cell motility, and in alterations of the membrane that accompany certain activities such as bone resorption by osteoclasts. Dynamins bind many proteins that bind actin and other cytoskeletal proteins. Dynamins can also self-assemble, a process that stimulates GTPase activity. Five alternatively spliced transcripts encoding different proteins have been described. Additional alternatively spliced transcripts may exist, but their full-length nature has not been determined. [provided by RefSeq, Jun 2010]","start":10718079,"end":10833488,"strand":1,"description":"dynamin 2 [Source:HGNC Symbol;Acc:HGNC:2974]"}, {"versioned_ensembl_gene_id":"ENSG00000256678.1","gene_symbol":"AC025423.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":68805011,"end":68805479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242741.1","gene_symbol":"LINC02005","gene_name":"long intergenic non-protein coding RNA 2005 [Source:HGNC Symbol;Acc:HGNC:52839]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105377165","summary":null,"start":73808601,"end":73902866,"strand":1,"description":"long intergenic non-protein coding RNA 2005 [Source:HGNC Symbol;Acc:HGNC:52839]"}, {"versioned_ensembl_gene_id":"ENSG00000282320.1","gene_symbol":"AC245427.6","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142786880,"end":142786927,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127129.9","gene_symbol":"EDN2","gene_name":"endothelin 2 [Source:HGNC Symbol;Acc:HGNC:3177]","synonyms":"ET2","biotype":"protein_coding","ncbi_id":"1907","summary":"This gene encodes a member of the endothelin protein family of secretory vasoconstrictive peptides. The preproprotein is processed to a short mature form which functions as a ligand for the endothelin receptors that initiate intracellular signaling events. This gene product is involved in a wide range of biological processes, such as hypertension and ovulation. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]","start":41478775,"end":41484673,"strand":-1,"description":"endothelin 2 [Source:HGNC Symbol;Acc:HGNC:3177]"}, {"versioned_ensembl_gene_id":"ENSG00000277270.1","gene_symbol":"AL160412.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61434625,"end":61437547,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215039.6","gene_symbol":"CD27-AS1","gene_name":"CD27 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43896]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"678655","summary":null,"start":6439001,"end":6451567,"strand":-1,"description":"CD27 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43896]"}, {"versioned_ensembl_gene_id":"ENSG00000282420.1","gene_symbol":"AC245427.7","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142787017,"end":142787064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239454.1","gene_symbol":"LINC02047","gene_name":"long intergenic non-protein coding RNA 2047 [Source:HGNC Symbol;Acc:HGNC:52887]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927346","summary":null,"start":73999805,"end":74005609,"strand":1,"description":"long intergenic non-protein coding RNA 2047 [Source:HGNC Symbol;Acc:HGNC:52887]"}, {"versioned_ensembl_gene_id":"ENSG00000224891.1","gene_symbol":"AC007899.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":37148530,"end":37149304,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282133.1","gene_symbol":"AC245427.4","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142787630,"end":142787679,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179242.15","gene_symbol":"CDH4","gene_name":"cadherin 4 [Source:HGNC Symbol;Acc:HGNC:1763]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1002","summary":"This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Based on studies in chicken and mouse, this cadherin is thought to play an important role during brain segmentation and neuronal outgrowth. In addition, a role in kidney and muscle development is indicated. Of particular interest are studies showing stable cis-heterodimers of cadherins 2 and 4 in cotransfected cell lines. Previously thought to interact in an exclusively homophilic manner, this is the first evidence of cadherin heterodimerization. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]","start":61252426,"end":61940617,"strand":1,"description":"cadherin 4 [Source:HGNC Symbol;Acc:HGNC:1763]"}, {"versioned_ensembl_gene_id":"ENSG00000281958.1","gene_symbol":"AC245427.3","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142788225,"end":142788275,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100249.4","gene_symbol":"C22orf31","gene_name":"chromosome 22 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26931]","synonyms":"HS747E2A,bK747E2.1","biotype":"protein_coding","ncbi_id":"25770","summary":null,"start":29058672,"end":29061844,"strand":-1,"description":"chromosome 22 open reading frame 31 [Source:HGNC Symbol;Acc:HGNC:26931]"}, {"versioned_ensembl_gene_id":"ENSG00000280285.1","gene_symbol":"AC108215.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":56662469,"end":56665694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171476.21","gene_symbol":"HOPX","gene_name":"HOP homeobox [Source:HGNC Symbol;Acc:HGNC:24961]","synonyms":"SMAP31,OB1,NECC1,LAGY,HOP","biotype":"protein_coding","ncbi_id":"84525","summary":"The protein encoded by this gene is a homeodomain protein that lacks certain conserved residues required for DNA binding. It was reported that choriocarcinoma cell lines and tissues failed to express this gene, which suggested the possible involvement of this gene in malignant conversion of placental trophoblasts. Studies in mice suggest that this protein may interact with serum response factor (SRF) and modulate SRF-dependent cardiac-specific gene expression and cardiac development. Multiple alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Feb 2009]","start":56647988,"end":56681899,"strand":-1,"description":"HOP homeobox [Source:HGNC Symbol;Acc:HGNC:24961]"}, {"versioned_ensembl_gene_id":"ENSG00000260814.2","gene_symbol":"AC073657.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41770756,"end":41772732,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173230.15","gene_symbol":"GOLGB1","gene_name":"golgin B1 [Source:HGNC Symbol;Acc:HGNC:4429]","synonyms":"GOLIM1,giantin,GCP372,GCP","biotype":"protein_coding","ncbi_id":"2804","summary":null,"start":121663199,"end":121749767,"strand":-1,"description":"golgin B1 [Source:HGNC Symbol;Acc:HGNC:4429]"}, {"versioned_ensembl_gene_id":"ENSG00000010610.9","gene_symbol":"CD4","gene_name":"CD4 molecule [Source:HGNC Symbol;Acc:HGNC:1678]","synonyms":null,"biotype":"protein_coding","ncbi_id":"920","summary":"This gene encodes the CD4 membrane glycoprotein of T lymphocytes. The CD4 antigen acts as a coreceptor with the T-cell receptor on the T lymphocyte to recognize antigens displayed by an antigen presenting cell in the context of class II MHC molecules. The CD4 antigen is also a primary receptor for entry of the human immunodeficiency virus through interactions with the HIV Env gp120 subunit. This gene is expressed not only in T lymphocytes, but also in B cells, macrophages, granulocytes, as well as in various regions of the brain. The protein functions to initiate or augment the early phase of T-cell activation, and may function as an important mediator of indirect neuronal damage in infectious and immune-mediated diseases of the central nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, May 2020]","start":6786858,"end":6820808,"strand":1,"description":"CD4 molecule [Source:HGNC Symbol;Acc:HGNC:1678]"}, {"versioned_ensembl_gene_id":"ENSG00000174197.16","gene_symbol":"MGA","gene_name":"MGA, MAX dimerization protein [Source:HGNC Symbol;Acc:HGNC:14010]","synonyms":"MXD5,MAD5,KIAA0518,FLJ12634","biotype":"protein_coding","ncbi_id":"23269","summary":null,"start":41621224,"end":41773081,"strand":1,"description":"MGA, MAX dimerization protein [Source:HGNC Symbol;Acc:HGNC:14010]"}, {"versioned_ensembl_gene_id":"ENSG00000126016.15","gene_symbol":"AMOT","gene_name":"angiomotin [Source:HGNC Symbol;Acc:HGNC:17810]","synonyms":"KIAA1071","biotype":"protein_coding","ncbi_id":"154796","summary":"This gene belongs to the motin family of angiostatin binding proteins characterized by conserved coiled-coil domains and C-terminal PDZ binding motifs. The encoded protein is expressed predominantly in endothelial cells of capillaries as well as larger vessels of the placenta where it may mediate the inhibitory effect of angiostatin on tube formation and the migration of endothelial cells toward growth factors during the formation of new blood vessels. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":112774503,"end":112840815,"strand":-1,"description":"angiomotin [Source:HGNC Symbol;Acc:HGNC:17810]"}, {"versioned_ensembl_gene_id":"ENSG00000248235.6","gene_symbol":"AC037459.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22589274,"end":22602084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262081.2","gene_symbol":"AP001005.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":80140,"end":88570,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229928.1","gene_symbol":"LINC00400","gene_name":"long intergenic non-protein coding RNA 400 [Source:HGNC Symbol;Acc:HGNC:42729]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874159","summary":null,"start":43158631,"end":43159466,"strand":1,"description":"long intergenic non-protein coding RNA 400 [Source:HGNC Symbol;Acc:HGNC:42729]"}, {"versioned_ensembl_gene_id":"ENSG00000227766.1","gene_symbol":"AL671277.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29942075,"end":29943067,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230795.3","gene_symbol":"HLA-K","gene_name":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]","synonyms":"HLA-70,HLAK,HLA70","biotype":"unprocessed_pseudogene","ncbi_id":"3138","summary":null,"start":29926459,"end":29929232,"strand":1,"description":"major histocompatibility complex, class I, K (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4969]"}, {"versioned_ensembl_gene_id":"ENSG00000276569.1","gene_symbol":"AL138709.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43179501,"end":43181193,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228071.4","gene_symbol":"RPL7P47","gene_name":"ribosomal protein L7 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:35913]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"146110","summary":null,"start":17932720,"end":17933275,"strand":1,"description":"ribosomal protein L7 pseudogene 47 [Source:HGNC Symbol;Acc:HGNC:35913]"}, {"versioned_ensembl_gene_id":"ENSG00000260933.1","gene_symbol":"AC091489.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18170356,"end":18170959,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000147168.12","gene_symbol":"IL2RG","gene_name":"interleukin 2 receptor subunit gamma [Source:HGNC Symbol;Acc:HGNC:6010]","synonyms":"CD132,SCIDX1,IMD4,CIDX","biotype":"protein_coding","ncbi_id":"3561","summary":"The protein encoded by this gene is an important signaling component of many interleukin receptors, including those of interleukin -2, -4, -7 and -21, and is thus referred to as the common gamma chain. Mutations in this gene cause X-linked severe combined immunodeficiency (XSCID), as well as X-linked combined immunodeficiency (XCID), a less severe immunodeficiency disorder. [provided by RefSeq, Mar 2010]","start":71107404,"end":71112108,"strand":-1,"description":"interleukin 2 receptor subunit gamma [Source:HGNC Symbol;Acc:HGNC:6010]"}, {"versioned_ensembl_gene_id":"ENSG00000229142.1","gene_symbol":"HCG4P8","gene_name":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]","synonyms":"HCGIV-08,HCGIV.7,HCGIV-8","biotype":"unprocessed_pseudogene","ncbi_id":"353005","summary":null,"start":29827385,"end":29828364,"strand":-1,"description":"HLA complex group 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:22927]"}, {"versioned_ensembl_gene_id":"ENSG00000276718.1","gene_symbol":"AC005840.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6466537,"end":6467135,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229390.1","gene_symbol":"MICD","gene_name":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]","synonyms":"PERB11.4","biotype":"unprocessed_pseudogene","ncbi_id":"4279","summary":null,"start":29970801,"end":29972464,"strand":-1,"description":"MHC class I polypeptide-related sequence D (pseudogene) [Source:HGNC Symbol;Acc:HGNC:7093]"}, {"versioned_ensembl_gene_id":"ENSG00000067836.12","gene_symbol":"ROGDI","gene_name":"rogdi homolog [Source:HGNC Symbol;Acc:HGNC:29478]","synonyms":"FLJ22386","biotype":"protein_coding","ncbi_id":"79641","summary":"This gene encodes a protein of unknown function. Loss-of-function mutation in this gene cause Kohlschutter-Tonz syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]","start":4796968,"end":4802950,"strand":-1,"description":"rogdi homolog [Source:HGNC Symbol;Acc:HGNC:29478]"}, {"versioned_ensembl_gene_id":"ENSG00000139193.3","gene_symbol":"CD27","gene_name":"CD27 molecule [Source:HGNC Symbol;Acc:HGNC:11922]","synonyms":"Tp55,TNFRSF7,S152","biotype":"protein_coding","ncbi_id":"939","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is required for generation and long-term maintenance of T cell immunity. It binds to ligand CD70, and plays a key role in regulating B-cell activation and immunoglobulin synthesis. This receptor transduces signals that lead to the activation of NF-kappaB and MAPK8/JNK. Adaptor proteins TRAF2 and TRAF5 have been shown to mediate the signaling process of this receptor. CD27-binding protein (SIVA), a proapoptotic protein, can bind to this receptor and is thought to play an important role in the apoptosis induced by this receptor. [provided by RefSeq, Jul 2008]","start":6444867,"end":6451718,"strand":1,"description":"CD27 molecule [Source:HGNC Symbol;Acc:HGNC:11922]"}, {"versioned_ensembl_gene_id":"ENSG00000235205.1","gene_symbol":"TATDN2P3","gene_name":"TatD DNase domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39256]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420458","summary":null,"start":23243520,"end":23247184,"strand":1,"description":"TatD DNase domain containing 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39256]"}, {"versioned_ensembl_gene_id":"ENSG00000260945.1","gene_symbol":"AC109495.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17540331,"end":17540985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236803.1","gene_symbol":"SDAD1P4","gene_name":"SDA1 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39261]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419955","summary":null,"start":23267506,"end":23269150,"strand":1,"description":"SDA1 domain containing 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:39261]"}, {"versioned_ensembl_gene_id":"ENSG00000102683.7","gene_symbol":"SGCG","gene_name":"sarcoglycan gamma [Source:HGNC Symbol;Acc:HGNC:10809]","synonyms":"MAM,LGMD2C,DMDA1,DMDA,DAGA4,TYPE,A4,SCG3,SCARMD2,MGC130048","biotype":"protein_coding","ncbi_id":"6445","summary":"This gene encodes gamma-sarcoglycan, one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin. The dystrophin-glycoprotein complex (DGC) spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C). [provided by RefSeq, Oct 2008]","start":23180952,"end":23325165,"strand":1,"description":"sarcoglycan gamma [Source:HGNC Symbol;Acc:HGNC:10809]"}, {"versioned_ensembl_gene_id":"ENSG00000134115.12","gene_symbol":"CNTN6","gene_name":"contactin 6 [Source:HGNC Symbol;Acc:HGNC:2176]","synonyms":"NB-3","biotype":"protein_coding","ncbi_id":"27255","summary":"The protein encoded by this gene is a member of the immunoglobulin superfamily. It is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":1092576,"end":1404217,"strand":1,"description":"contactin 6 [Source:HGNC Symbol;Acc:HGNC:2176]"}, {"versioned_ensembl_gene_id":"ENSG00000261555.1","gene_symbol":"AC025277.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17825252,"end":17826906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280042.1","gene_symbol":"AC022336.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":124791119,"end":124793104,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102038.15","gene_symbol":"SMARCA1","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 [Source:HGNC Symbol;Acc:HGNC:11097]","synonyms":"ISWI,hSNF2L,SWI,SNF2LB,SNF2L1,SNF2L,NURF140","biotype":"protein_coding","ncbi_id":"6594","summary":"This gene encodes a member of the SWI/SNF family of proteins. The encoded protein is an ATPase which is expressed in diverse tissues and contributes to the chromatin remodeling complex that is involved in transcription. The protein may also play a role in DNA damage, growth inhibition and apoptosis of cancer cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]","start":129446501,"end":129523500,"strand":-1,"description":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 [Source:HGNC Symbol;Acc:HGNC:11097]"}, {"versioned_ensembl_gene_id":"ENSG00000243986.2","gene_symbol":"ENO1P3","gene_name":"enolase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37944]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419069","summary":null,"start":124862094,"end":124863317,"strand":-1,"description":"enolase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37944]"}, {"versioned_ensembl_gene_id":"ENSG00000082781.11","gene_symbol":"ITGB5","gene_name":"integrin subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:6160]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3693","summary":"This gene encodes a beta subunit of integrin, which can combine with different alpha chains to form a variety of integrin heterodimers. Integrins are integral cell-surface receptors that participate in cell adhesion as well as cell-surface mediated signaling. The alphav beta5 integrin is involved in adhesion to vitronectin. [provided by RefSeq, Aug 2017]","start":124761948,"end":124901418,"strand":-1,"description":"integrin subunit beta 5 [Source:HGNC Symbol;Acc:HGNC:6160]"}, {"versioned_ensembl_gene_id":"ENSG00000231102.1","gene_symbol":"AL035588.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41720396,"end":41734032,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260242.1","gene_symbol":"AC091489.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":18002806,"end":18173063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280283.1","gene_symbol":"AC010601.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":17961597,"end":17962370,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214289.2","gene_symbol":"RPL39P5","gene_name":"ribosomal protein L39 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:26015]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"553117","summary":null,"start":134351852,"end":134356561,"strand":-1,"description":"ribosomal protein L39 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:26015]"}, {"versioned_ensembl_gene_id":"ENSG00000259929.5","gene_symbol":"AC010601.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":17933189,"end":18151595,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270258.1","gene_symbol":"DUXAP4","gene_name":"double homeobox A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32183]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"503633","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DUXA homeobox gene family. [provided by RefSeq, Jul 2008]","start":45055656,"end":45056268,"strand":1,"description":"double homeobox A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32183]"}, {"versioned_ensembl_gene_id":"ENSG00000165511.6","gene_symbol":"C10orf25","gene_name":"chromosome 10 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:23509]","synonyms":"FLJ30567","biotype":"antisense_RNA","ncbi_id":"220979","summary":null,"start":44997698,"end":45000888,"strand":-1,"description":"chromosome 10 open reading frame 25 [Source:HGNC Symbol;Acc:HGNC:23509]"}, {"versioned_ensembl_gene_id":"ENSG00000259280.1","gene_symbol":"AC018563.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":36876379,"end":36887035,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172940.11","gene_symbol":"SLC22A13","gene_name":"solute carrier family 22 member 13 [Source:HGNC Symbol;Acc:HGNC:8494]","synonyms":"ORCTL3,OCTL3,OCTL1,OAT10","biotype":"protein_coding","ncbi_id":"9390","summary":"This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 4. The encoded protein is a transmembrane protein involved in the transport of small molecules. This protein can function to mediate urate uptake and is a high affinity nicotinate exchanger in the kidneys and the intestine. [provided by RefSeq, Sep 2008]","start":38265812,"end":38278315,"strand":1,"description":"solute carrier family 22 member 13 [Source:HGNC Symbol;Acc:HGNC:8494]"}, {"versioned_ensembl_gene_id":"ENSG00000235690.2","gene_symbol":"CUBNP3","gene_name":"cubilin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44985]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421634","summary":null,"start":45127318,"end":45148914,"strand":1,"description":"cubilin pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44985]"}, {"versioned_ensembl_gene_id":"ENSG00000250223.1","gene_symbol":"LINC01216","gene_name":"long intergenic non-protein coding RNA 1216 [Source:HGNC Symbol;Acc:HGNC:41418]","synonyms":"EMCN-IT3","biotype":"sense_intronic","ncbi_id":"100874275","summary":null,"start":100660279,"end":100675113,"strand":-1,"description":"long intergenic non-protein coding RNA 1216 [Source:HGNC Symbol;Acc:HGNC:41418]"}, {"versioned_ensembl_gene_id":"ENSG00000236442.1","gene_symbol":"ANKRD54P1","gene_name":"ankyrin repeat domain 54 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39214]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419962","summary":null,"start":45151445,"end":45151915,"strand":-1,"description":"ankyrin repeat domain 54 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39214]"}, {"versioned_ensembl_gene_id":"ENSG00000277757.4","gene_symbol":"AL358394.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45016080,"end":45147221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000164035.9","gene_symbol":"EMCN","gene_name":"endomucin [Source:HGNC Symbol;Acc:HGNC:16041]","synonyms":"MUC14","biotype":"protein_coding","ncbi_id":"51705","summary":"EMCN is a mucin-like sialoglycoprotein that interferes with the assembly of focal adhesion complexes and inhibits interaction between cells and the extracellular matrix (Kinoshita et al., 2001 [PubMed 11418125]).[supplied by OMIM, Mar 2008]","start":100395341,"end":100880126,"strand":-1,"description":"endomucin [Source:HGNC Symbol;Acc:HGNC:16041]"}, {"versioned_ensembl_gene_id":"ENSG00000228462.1","gene_symbol":"RPS19P7","gene_name":"ribosomal protein S19 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35550]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728509","summary":null,"start":45073146,"end":45073541,"strand":-1,"description":"ribosomal protein S19 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:35550]"}, {"versioned_ensembl_gene_id":"ENSG00000226937.9","gene_symbol":"CEP164P1","gene_name":"centrosomal protein 164 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44988]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100289237","summary":null,"start":45002222,"end":45076066,"strand":-1,"description":"centrosomal protein 164 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44988]"}, {"versioned_ensembl_gene_id":"ENSG00000280930.1","gene_symbol":"AC226374.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189977577,"end":189977825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237782.3","gene_symbol":"AL020989.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45381527,"end":45381995,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224541.1","gene_symbol":"AP001439.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":26158091,"end":26175824,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280732.1","gene_symbol":"AF146191.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189983880,"end":189984585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173876.10","gene_symbol":"TUBB7P","gene_name":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]","synonyms":"TUBB4Q","biotype":"unprocessed_pseudogene","ncbi_id":"56604","summary":null,"start":189986501,"end":189988849,"strand":-1,"description":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]"}, {"versioned_ensembl_gene_id":"ENSG00000275312.1","gene_symbol":"AL512324.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45180400,"end":45180616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227683.1","gene_symbol":"AL358394.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45164228,"end":45181427,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142192.20","gene_symbol":"APP","gene_name":"amyloid beta precursor protein [Source:HGNC Symbol;Acc:HGNC:620]","synonyms":"AD1","biotype":"protein_coding","ncbi_id":"351","summary":"This gene encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. In addition, two of the peptides are antimicrobial peptides, having been shown to have bacteriocidal and antifungal activities. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2014]","start":25880550,"end":26171128,"strand":-1,"description":"amyloid beta precursor protein [Source:HGNC Symbol;Acc:HGNC:620]"}, {"versioned_ensembl_gene_id":"ENSG00000243349.2","gene_symbol":"AL358394.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":45147394,"end":45171389,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229563.6","gene_symbol":"LINC01204","gene_name":"long intergenic non-protein coding RNA 1204 [Source:HGNC Symbol;Acc:HGNC:49635]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927528","summary":null,"start":45505388,"end":45630202,"strand":1,"description":"long intergenic non-protein coding RNA 1204 [Source:HGNC Symbol;Acc:HGNC:49635]"}, {"versioned_ensembl_gene_id":"ENSG00000232554.8","gene_symbol":"RSU1P2","gene_name":"Ras suppressor protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44391]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100133308","summary":null,"start":45099487,"end":45154596,"strand":-1,"description":"Ras suppressor protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44391]"}, {"versioned_ensembl_gene_id":"ENSG00000276616.2","gene_symbol":"DUX4L9","gene_name":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288711","summary":null,"start":190025385,"end":190026643,"strand":-1,"description":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]"}, {"versioned_ensembl_gene_id":"ENSG00000166681.13","gene_symbol":"BEX3","gene_name":"brain expressed X-linked 3 [Source:HGNC Symbol;Acc:HGNC:13388]","synonyms":"NGFRAP1,NADE,HGR74,DXS6984E,Bex","biotype":"protein_coding","ncbi_id":"27018","summary":null,"start":103376340,"end":103378077,"strand":1,"description":"brain expressed X-linked 3 [Source:HGNC Symbol;Acc:HGNC:13388]"}, {"versioned_ensembl_gene_id":"ENSG00000250398.1","gene_symbol":"AC097467.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":155383107,"end":155384102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270541.1","gene_symbol":"AC069545.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":55746551,"end":55746908,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237982.1","gene_symbol":"AP006193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38270283,"end":38270767,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271606.1","gene_symbol":"AC097467.4","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":155385352,"end":155385492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249247.1","gene_symbol":"MTCYBP17","gene_name":"mitochondrially encoded cytochrome b pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51970]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075213","summary":null,"start":155451617,"end":155452405,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:51970]"}, {"versioned_ensembl_gene_id":"ENSG00000225106.1","gene_symbol":"AL162457.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61738219,"end":61755056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249770.1","gene_symbol":"MTND6P17","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39480]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106480728","summary":null,"start":155452526,"end":155453044,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:39480]"}, {"versioned_ensembl_gene_id":"ENSG00000248748.1","gene_symbol":"MTND5P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42305]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873199","summary":null,"start":155453049,"end":155454803,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42305]"}, {"versioned_ensembl_gene_id":"ENSG00000230501.1","gene_symbol":"ANKRD30BP3","gene_name":"ankyrin repeat domain 30B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27873]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"338579","summary":null,"start":45156775,"end":45176925,"strand":1,"description":"ankyrin repeat domain 30B pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:27873]"}, {"versioned_ensembl_gene_id":"ENSG00000179253.3","gene_symbol":"AL162457.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":61717506,"end":61719748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248548.1","gene_symbol":"MTND4P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42227]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873194","summary":null,"start":155455050,"end":155456411,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42227]"}, {"versioned_ensembl_gene_id":"ENSG00000276786.1","gene_symbol":"BX640515.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":61369879,"end":61370855,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249127.1","gene_symbol":"MTND3P3","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42155]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873187","summary":null,"start":155456638,"end":155456981,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42155]"}, {"versioned_ensembl_gene_id":"ENSG00000165512.4","gene_symbol":"ZNF22","gene_name":"zinc finger protein 22 [Source:HGNC Symbol;Acc:HGNC:13012]","synonyms":"ZNF422,Zfp422,KOX15,HKR-T1","biotype":"protein_coding","ncbi_id":"7570","summary":null,"start":45000475,"end":45005326,"strand":1,"description":"zinc finger protein 22 [Source:HGNC Symbol;Acc:HGNC:13012]"}, {"versioned_ensembl_gene_id":"ENSG00000249698.1","gene_symbol":"MTCO3P9","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52039]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075269","summary":null,"start":155457180,"end":155457960,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52039]"}, {"versioned_ensembl_gene_id":"ENSG00000248420.1","gene_symbol":"MTATP6P9","gene_name":"mitochondrially encoded ATP synthase 6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44583]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"106479044","summary":null,"start":155457961,"end":155458640,"strand":-1,"description":"mitochondrially encoded ATP synthase 6 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:44583]"}, {"versioned_ensembl_gene_id":"ENSG00000249386.1","gene_symbol":"MTCO2P9","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52025]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075267","summary":null,"start":155458870,"end":155459563,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52025]"}, {"versioned_ensembl_gene_id":"ENSG00000251223.1","gene_symbol":"MTCO1P9","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52011]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"107075139","summary":null,"start":155459704,"end":155461237,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:52011]"}, {"versioned_ensembl_gene_id":"ENSG00000124097.7","gene_symbol":"HMGB1P1","gene_name":"high mobility group box 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4993]","synonyms":"HMGB1L1,HMG1L7,HMG1L1","biotype":"processed_pseudogene","ncbi_id":"10357","summary":"This gene may represent an evolving retropseudogene of the high-mobility group box 1 gene, which has multiple pseudogenes. This gene has an intact open reading frame, where the length of encoded protein is conserved, compared to the high-mobility group box 1 protein. However, due to the lack of conclusive evidence for specific transcription at this location, this locus is currently represented as a pseudogene. [provided by RefSeq, Jan 2010]","start":57488392,"end":57489027,"strand":-1,"description":"high mobility group box 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4993]"}, {"versioned_ensembl_gene_id":"ENSG00000100336.17","gene_symbol":"APOL4","gene_name":"apolipoprotein L4 [Source:HGNC Symbol;Acc:HGNC:14867]","synonyms":"APOLIV","biotype":"protein_coding","ncbi_id":"80832","summary":"This gene encodes a member of the apolipoprotein L family. The encoded protein may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2020]","start":36189124,"end":36204840,"strand":-1,"description":"apolipoprotein L4 [Source:HGNC Symbol;Acc:HGNC:14867]"}, {"versioned_ensembl_gene_id":"ENSG00000205213.13","gene_symbol":"LGR4","gene_name":"leucine rich repeat containing G protein-coupled receptor 4 [Source:HGNC Symbol;Acc:HGNC:13299]","synonyms":"GPR48","biotype":"protein_coding","ncbi_id":"55366","summary":"The protein encoded by this gene is a G-protein coupled receptor that binds R-spondins and activates the Wnt signaling pathway. This Wnt signaling pathway activation is necessary for proper development of many organs of the body. [provided by RefSeq, Oct 2016]","start":27365961,"end":27472775,"strand":-1,"description":"leucine rich repeat containing G protein-coupled receptor 4 [Source:HGNC Symbol;Acc:HGNC:13299]"}, {"versioned_ensembl_gene_id":"ENSG00000248155.1","gene_symbol":"CR545473.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":2607870,"end":2608146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125652.7","gene_symbol":"ALKBH7","gene_name":"alkB homolog 7 [Source:HGNC Symbol;Acc:HGNC:21306]","synonyms":"SPATA11,MGC10974","biotype":"protein_coding","ncbi_id":"84266","summary":null,"start":6372433,"end":6375251,"strand":1,"description":"alkB homolog 7 [Source:HGNC Symbol;Acc:HGNC:21306]"}, {"versioned_ensembl_gene_id":"ENSG00000218198.3","gene_symbol":"RPS20P32","gene_name":"ribosomal protein S20 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36444]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129306","summary":null,"start":27017554,"end":27017909,"strand":-1,"description":"ribosomal protein S20 pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:36444]"}, {"versioned_ensembl_gene_id":"ENSG00000122952.16","gene_symbol":"ZWINT","gene_name":"ZW10 interacting kinetochore protein [Source:HGNC Symbol;Acc:HGNC:13195]","synonyms":"Zwint1,SIP30,KNTC2AP","biotype":"protein_coding","ncbi_id":"11130","summary":"This gene encodes a protein that is clearly involved in kinetochore function although an exact role is not known. It interacts with ZW10, another kinetochore protein, possibly regulating the association between ZW10 and kinetochores. The encoded protein localizes to prophase kinetochores before ZW10 does and it remains detectable on the kinetochore until late anaphase. It has a uniform distribution in the cytoplasm of interphase cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":56357228,"end":56361275,"strand":-1,"description":"ZW10 interacting kinetochore protein [Source:HGNC Symbol;Acc:HGNC:13195]"}, {"versioned_ensembl_gene_id":"ENSG00000267157.1","gene_symbol":"AC011499.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5784005,"end":5785619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242915.1","gene_symbol":"SNRPGP7","gene_name":"small nuclear ribonucleoprotein polypeptide G pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39326]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874408","summary":null,"start":28460256,"end":28460361,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide G pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:39326]"}, {"versioned_ensembl_gene_id":"ENSG00000212123.3","gene_symbol":"PRR22","gene_name":"proline rich 22 [Source:HGNC Symbol;Acc:HGNC:28354]","synonyms":"MGC24975","biotype":"protein_coding","ncbi_id":"163154","summary":null,"start":5782960,"end":5784765,"strand":-1,"description":"proline rich 22 [Source:HGNC Symbol;Acc:HGNC:28354]"}, {"versioned_ensembl_gene_id":"ENSG00000230730.1","gene_symbol":"AC074011.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28633282,"end":28664540,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186501.14","gene_symbol":"TMEM222","gene_name":"transmembrane protein 222 [Source:HGNC Symbol;Acc:HGNC:25363]","synonyms":"DKFZP564D0478,C1orf160","biotype":"protein_coding","ncbi_id":"84065","summary":null,"start":27322145,"end":27336400,"strand":1,"description":"transmembrane protein 222 [Source:HGNC Symbol;Acc:HGNC:25363]"}, {"versioned_ensembl_gene_id":"ENSG00000270048.1","gene_symbol":"AC068790.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123962555,"end":123962817,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270095.1","gene_symbol":"AC068790.6","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":123971457,"end":123971714,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163803.12","gene_symbol":"PLB1","gene_name":"phospholipase B1 [Source:HGNC Symbol;Acc:HGNC:30041]","synonyms":"PLB,FLJ30866","biotype":"protein_coding","ncbi_id":"151056","summary":"This gene encodes a membrane-associated phospholipase that displays lysophospholipase and phospholipase A2 activities through removal of sn-1 and sn-2 fatty acids of glycerophospholipids. In addition, it displays lipase and retinyl ester hydrolase activities. The encoded protein is highly conserved and is composed of a large, glycosylated extracellular domain composed of four tandem homologous domains, followed by a hydrophobic segment that anchors the enzyme to the membrane and a short C-terminal cytoplasmic tail. This gene has been identified as a candidate rheumatoid arthritis risk gene. [provided by RefSeq, Jul 2016]","start":28457145,"end":28643788,"strand":1,"description":"phospholipase B1 [Source:HGNC Symbol;Acc:HGNC:30041]"}, {"versioned_ensembl_gene_id":"ENSG00000178882.14","gene_symbol":"RFLNA","gene_name":"refilin A [Source:HGNC Symbol;Acc:HGNC:27051]","synonyms":"RefilinA,FLJ44614,FAM101A,Cfm2","biotype":"protein_coding","ncbi_id":"144347","summary":null,"start":123973241,"end":124316024,"strand":1,"description":"refilin A [Source:HGNC Symbol;Acc:HGNC:27051]"}, {"versioned_ensembl_gene_id":"ENSG00000101844.17","gene_symbol":"ATG4A","gene_name":"autophagy related 4A cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16489]","synonyms":"AUTL2,APG4A","biotype":"protein_coding","ncbi_id":"115201","summary":"Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. [provided by RefSeq, Mar 2016]","start":108091668,"end":108154671,"strand":1,"description":"autophagy related 4A cysteine peptidase [Source:HGNC Symbol;Acc:HGNC:16489]"}, {"versioned_ensembl_gene_id":"ENSG00000263460.1","gene_symbol":"BOD1P1","gene_name":"biorientation of chromosomes in cell division 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51435]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"100129468","summary":null,"start":3415145,"end":3415580,"strand":1,"description":"biorientation of chromosomes in cell division 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51435]"}, {"versioned_ensembl_gene_id":"ENSG00000162688.16","gene_symbol":"AGL","gene_name":"amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase [Source:HGNC Symbol;Acc:HGNC:321]","synonyms":null,"biotype":"protein_coding","ncbi_id":"178","summary":"This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":99850084,"end":99924023,"strand":1,"description":"amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase [Source:HGNC Symbol;Acc:HGNC:321]"}, {"versioned_ensembl_gene_id":"ENSG00000125650.4","gene_symbol":"PSPN","gene_name":"persephin [Source:HGNC Symbol;Acc:HGNC:9579]","synonyms":"PSP","biotype":"protein_coding","ncbi_id":"5623","summary":"This gene encodes a secreted ligand of the GDNF (glial cell line-derived neurotrophic factor) subfamily and TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein signals through the RET receptor tyrosine kinase and a GPI-linked coreceptor, and promotes survival of neuronal populations. This protein may play a role in cell death, and nervous system development and function. Elevated expression of this gene has been observed in oral squamous cell carcinoma. [provided by RefSeq, Aug 2016]","start":6375148,"end":6379058,"strand":-1,"description":"persephin [Source:HGNC Symbol;Acc:HGNC:9579]"}, {"versioned_ensembl_gene_id":"ENSG00000143452.15","gene_symbol":"HORMAD1","gene_name":"HORMA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25245]","synonyms":"DKFZP434A1315,CT46","biotype":"protein_coding","ncbi_id":"84072","summary":"This gene encodes a HORMA domain-containing protein. HORMA domains are involved in chromatin binding and play a role in cell cycle regulation. The encoded protein may play a role in meiosis, and expression of this gene is a potential marker for cancer. A pseudogene of this gene is located on the long arm of chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]","start":150698060,"end":150720888,"strand":-1,"description":"HORMA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25245]"}, {"versioned_ensembl_gene_id":"ENSG00000261217.2","gene_symbol":"BCAP31P1","gene_name":"B-cell receptor-associated protein 31 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51323]","synonyms":"TCONS_l2_00010135","biotype":"unprocessed_pseudogene","ncbi_id":"100194425","summary":null,"start":33988406,"end":33991551,"strand":-1,"description":"B-cell receptor-associated protein 31 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51323]"}, {"versioned_ensembl_gene_id":"ENSG00000259990.2","gene_symbol":"AC133561.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34013394,"end":34013830,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283065.1","gene_symbol":"AC133561.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34015260,"end":34015477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000019991.15","gene_symbol":"HGF","gene_name":"hepatocyte growth factor [Source:HGNC Symbol;Acc:HGNC:4893]","synonyms":"F-TCF,DFNB39,SF,HPTA,HGFB","biotype":"protein_coding","ncbi_id":"3082","summary":"This gene encodes a protein that binds to the hepatocyte growth factor receptor to regulate cell growth, cell motility and morphogenesis in numerous cell and tissue types. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate alpha and beta chains, which form the mature heterodimer. This protein is secreted by mesenchymal cells and acts as a multi-functional cytokine on cells of mainly epithelial origin. This protein also plays a role in angiogenesis, tumorogenesis, and tissue regeneration. Although the encoded protein is a member of the peptidase S1 family of serine proteases, it lacks peptidase activity. Mutations in this gene are associated with nonsyndromic hearing loss. [provided by RefSeq, Nov 2015]","start":81699006,"end":81770438,"strand":-1,"description":"hepatocyte growth factor [Source:HGNC Symbol;Acc:HGNC:4893]"}, {"versioned_ensembl_gene_id":"ENSG00000223765.2","gene_symbol":"LINC01626","gene_name":"long intergenic non-protein coding RNA 1626 [Source:HGNC Symbol;Acc:HGNC:52257]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724000","summary":null,"start":71450834,"end":71458874,"strand":1,"description":"long intergenic non-protein coding RNA 1626 [Source:HGNC Symbol;Acc:HGNC:52257]"}, {"versioned_ensembl_gene_id":"ENSG00000110756.17","gene_symbol":"HPS5","gene_name":"HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 [Source:HGNC Symbol;Acc:HGNC:17022]","synonyms":"RU2,BLOC2S2,AIBP63","biotype":"protein_coding","ncbi_id":"11234","summary":"This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of integrin, alpha-3. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 5. Multiple transcript variants encoding two distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":18278668,"end":18322198,"strand":-1,"description":"HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 [Source:HGNC Symbol;Acc:HGNC:17022]"}, {"versioned_ensembl_gene_id":"ENSG00000219575.1","gene_symbol":"AL035467.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":71550958,"end":71551643,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000218014.1","gene_symbol":"KRT19P1","gene_name":"keratin 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33422]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441160","summary":null,"start":71584721,"end":71585906,"strand":1,"description":"keratin 19 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33422]"}, {"versioned_ensembl_gene_id":"ENSG00000270702.1","gene_symbol":"AC073657.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41718370,"end":41718672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000133863.7","gene_symbol":"TEX15","gene_name":"testis expressed 15, meiosis and synapsis associated [Source:HGNC Symbol;Acc:HGNC:11738]","synonyms":"CT42","biotype":"protein_coding","ncbi_id":"56154","summary":"This gene encodes a protein that is required for DNA double-strand break repair, chromosome synapsis, and meiotic recombination in spermatocytes. Male mice with a knockout of the orthologous gene are viable but sterile. Loss-of-function mutations in the orthologous mouse gene cause early meiotic arrest in spermatocytes, before the mid-pachytene stage. Naturally occurring mutations in this gene are associated with nonobstructive azoospermia. [provided by RefSeq, Apr 2017]","start":30831544,"end":30890606,"strand":-1,"description":"testis expressed 15, meiosis and synapsis associated [Source:HGNC Symbol;Acc:HGNC:11738]"}, {"versioned_ensembl_gene_id":"ENSG00000258352.1","gene_symbol":"AC119044.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":47135498,"end":47138370,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187980.6","gene_symbol":"PLA2G2C","gene_name":"phospholipase A2 group IIC [Source:HGNC Symbol;Acc:HGNC:9032]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391013","summary":null,"start":20161253,"end":20177424,"strand":-1,"description":"phospholipase A2 group IIC [Source:HGNC Symbol;Acc:HGNC:9032]"}, {"versioned_ensembl_gene_id":"ENSG00000088926.13","gene_symbol":"F11","gene_name":"coagulation factor XI [Source:HGNC Symbol;Acc:HGNC:3529]","synonyms":"FXI","biotype":"protein_coding","ncbi_id":"2160","summary":"This gene encodes coagulation factor XI of the blood coagulation cascade. This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by disulfide bonds. During activation of the plasma factor XI, an internal peptide bond is cleaved by factor XIIa (or XII) in each of the two chains, resulting in activated factor XIa, a serine protease composed of two heavy and two light chains held together by disulfide bonds. This activated plasma factor XI triggers the middle phase of the intrisic pathway of blood coagulation by activating factor IX. Defects in this factor lead to Rosenthal syndrome, a blood coagulation abnormality. [provided by RefSeq, Jul 2008]","start":186265945,"end":186288806,"strand":1,"description":"coagulation factor XI [Source:HGNC Symbol;Acc:HGNC:3529]"}, {"versioned_ensembl_gene_id":"ENSG00000274506.1","gene_symbol":"AC138832.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":70691064,"end":70691619,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139211.6","gene_symbol":"AMIGO2","gene_name":"adhesion molecule with Ig like domain 2 [Source:HGNC Symbol;Acc:HGNC:24073]","synonyms":"DEGA,ALI1","biotype":"protein_coding","ncbi_id":"347902","summary":null,"start":47075707,"end":47079951,"strand":-1,"description":"adhesion molecule with Ig like domain 2 [Source:HGNC Symbol;Acc:HGNC:24073]"}, {"versioned_ensembl_gene_id":"ENSG00000225986.1","gene_symbol":"UBXN10-AS1","gene_name":"UBXN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41141]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928017","summary":null,"start":20184242,"end":20186486,"strand":-1,"description":"UBXN10 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41141]"}, {"versioned_ensembl_gene_id":"ENSG00000226015.2","gene_symbol":"CCT8P1","gene_name":"chaperonin containing TCP1 subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35144]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644131","summary":null,"start":147203276,"end":147204932,"strand":-1,"description":"chaperonin containing TCP1 subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:35144]"}, {"versioned_ensembl_gene_id":"ENSG00000180867.10","gene_symbol":"PDIA3P1","gene_name":"protein disulfide isomerase family A member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4607]","synonyms":"PDIA3P,GRP58P","biotype":"processed_pseudogene","ncbi_id":"171423","summary":null,"start":147178113,"end":147179622,"strand":1,"description":"protein disulfide isomerase family A member 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:4607]"}, {"versioned_ensembl_gene_id":"ENSG00000237188.3","gene_symbol":"AC242426.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":147172771,"end":147211568,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177426.20","gene_symbol":"TGIF1","gene_name":"TGFB induced factor homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11776]","synonyms":"TGIF,HPE4","biotype":"protein_coding","ncbi_id":"7050","summary":"The protein encoded by this gene is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains. TALE homeobox proteins are highly conserved transcription regulators. This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter. In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element, the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult. Mutations in this gene are associated with holoprosencephaly type 4, which is a structural anomaly of the brain. Alternative splicing has been observed at this locus and multiple splice variants encoding distinct isoforms are described. [provided by RefSeq, Jul 2013]","start":3411608,"end":3459978,"strand":1,"description":"TGFB induced factor homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11776]"}, {"versioned_ensembl_gene_id":"ENSG00000162543.5","gene_symbol":"UBXN10","gene_name":"UBX domain protein 10 [Source:HGNC Symbol;Acc:HGNC:26354]","synonyms":"UBXD3,FLJ25429","biotype":"protein_coding","ncbi_id":"127733","summary":null,"start":20186085,"end":20196048,"strand":1,"description":"UBX domain protein 10 [Source:HGNC Symbol;Acc:HGNC:26354]"}, {"versioned_ensembl_gene_id":"ENSG00000278811.4","gene_symbol":"LINC00624","gene_name":"long intergenic non-protein coding RNA 624 [Source:HGNC Symbol;Acc:HGNC:44254]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100289211","summary":null,"start":147258885,"end":147517875,"strand":-1,"description":"long intergenic non-protein coding RNA 624 [Source:HGNC Symbol;Acc:HGNC:44254]"}, {"versioned_ensembl_gene_id":"ENSG00000223738.3","gene_symbol":"AC016930.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":74101349,"end":74103553,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179715.12","gene_symbol":"PCED1B","gene_name":"PC-esterase domain containing 1B [Source:HGNC Symbol;Acc:HGNC:28255]","synonyms":"MGC16044,FAM113B","biotype":"protein_coding","ncbi_id":"91523","summary":"This gene encodes a protein that belongs to the GDSL/SGNH-like acyl-esterase family. Members of this family are hydrolases thought to function in modification of biopolymers on the cell surface. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]","start":47079603,"end":47236662,"strand":1,"description":"PC-esterase domain containing 1B [Source:HGNC Symbol;Acc:HGNC:28255]"}, {"versioned_ensembl_gene_id":"ENSG00000213452.4","gene_symbol":"AKR1B1P2","gene_name":"aldo-keto reductase family 1 member B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:425]","synonyms":"ALDRP","biotype":"processed_pseudogene","ncbi_id":"236","summary":null,"start":74135959,"end":74136892,"strand":1,"description":"aldo-keto reductase family 1 member B1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:425]"}, {"versioned_ensembl_gene_id":"ENSG00000244286.1","gene_symbol":"ITGB5-AS1","gene_name":"ITGB5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40309]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873992","summary":null,"start":124781155,"end":124787757,"strand":1,"description":"ITGB5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40309]"}, {"versioned_ensembl_gene_id":"ENSG00000101670.11","gene_symbol":"LIPG","gene_name":"lipase G, endothelial type [Source:HGNC Symbol;Acc:HGNC:6623]","synonyms":"EDL","biotype":"protein_coding","ncbi_id":"9388","summary":"The protein encoded by this gene has substantial phospholipase activity and may be involved in lipoprotein metabolism and vascular biology. This protein is designated a member of the TG lipase family by its sequence and characteristic lid region which provides substrate specificity for enzymes of the TG lipase family. [provided by RefSeq, Jul 2008]","start":49560699,"end":49599182,"strand":1,"description":"lipase G, endothelial type [Source:HGNC Symbol;Acc:HGNC:6623]"}, {"versioned_ensembl_gene_id":"ENSG00000260910.1","gene_symbol":"LINC00565","gene_name":"long intergenic non-protein coding RNA 565 [Source:HGNC Symbol;Acc:HGNC:43709]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100861555","summary":null,"start":113926514,"end":113928844,"strand":-1,"description":"long intergenic non-protein coding RNA 565 [Source:HGNC Symbol;Acc:HGNC:43709]"}, {"versioned_ensembl_gene_id":"ENSG00000281936.1","gene_symbol":"AC133633.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2503318,"end":2506502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213226.4","gene_symbol":"AC242426.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":147319110,"end":147320224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229404.5","gene_symbol":"LINC00858","gene_name":"long intergenic non-protein coding RNA 858 [Source:HGNC Symbol;Acc:HGNC:27276]","synonyms":null,"biotype":"lincRNA","ncbi_id":"170425","summary":null,"start":84279980,"end":84294659,"strand":1,"description":"long intergenic non-protein coding RNA 858 [Source:HGNC Symbol;Acc:HGNC:27276]"}, {"versioned_ensembl_gene_id":"ENSG00000235217.6","gene_symbol":"TSPY26P","gene_name":"testis specific protein, Y-linked 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:16256]","synonyms":"TSPYL3,bA392M18.1","biotype":"transcribed_processed_pseudogene","ncbi_id":"128854","summary":null,"start":32186477,"end":32190527,"strand":-1,"description":"testis specific protein, Y-linked 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:16256]"}, {"versioned_ensembl_gene_id":"ENSG00000232575.10","gene_symbol":"TUBB","gene_name":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]","synonyms":"MGC16435,Tubb5,M40,OK/SW-cl.56","biotype":"protein_coding","ncbi_id":"203068","summary":"This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]","start":30764859,"end":30770084,"strand":1,"description":"tubulin beta class I [Source:HGNC Symbol;Acc:HGNC:20778]"}, {"versioned_ensembl_gene_id":"ENSG00000214110.3","gene_symbol":"LDHAP4","gene_name":"lactate dehydrogenase A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:6539]","synonyms":"LDHAL4","biotype":"processed_pseudogene","ncbi_id":"158222","summary":null,"start":14921337,"end":14922334,"strand":-1,"description":"lactate dehydrogenase A pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:6539]"}, {"versioned_ensembl_gene_id":"ENSG00000163645.14","gene_symbol":"ERICH6","gene_name":"glutamate rich 6 [Source:HGNC Symbol;Acc:HGNC:28602]","synonyms":"MGC39662,FAM194A,ERICH6A,C3orf44","biotype":"protein_coding","ncbi_id":"131831","summary":null,"start":150659885,"end":150703971,"strand":-1,"description":"glutamate rich 6 [Source:HGNC Symbol;Acc:HGNC:28602]"}, {"versioned_ensembl_gene_id":"ENSG00000103994.16","gene_symbol":"ZNF106","gene_name":"zinc finger protein 106 [Source:HGNC Symbol;Acc:HGNC:12886]","synonyms":"ZNF474,ZFP106,SH3BP3","biotype":"protein_coding","ncbi_id":"64397","summary":null,"start":42412823,"end":42491123,"strand":-1,"description":"zinc finger protein 106 [Source:HGNC Symbol;Acc:HGNC:12886]"}, {"versioned_ensembl_gene_id":"ENSG00000254862.5","gene_symbol":"AC100771.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":27471729,"end":27482433,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000247774.6","gene_symbol":"PCED1B-AS1","gene_name":"PCED1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44166]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100233209","summary":null,"start":47205898,"end":47216456,"strand":-1,"description":"PCED1B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44166]"}, {"versioned_ensembl_gene_id":"ENSG00000282397.1","gene_symbol":"AC104021.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2544294,"end":2607662,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000114742.13","gene_symbol":"WDR48","gene_name":"WD repeat domain 48 [Source:HGNC Symbol;Acc:HGNC:30914]","synonyms":"SPG60,P80,KIAA1449","biotype":"protein_coding","ncbi_id":"57599","summary":"The protein encoded by this gene has been shown to interact with ubiquitin specific peptidase 1 (USP1), activating the deubiquitinating activity of USP1 and allowing it to remove the ubiquitin moiety from monoubiquitinated FANCD2. FANCD2 is ubiquitinated in response to DNA damage. [provided by RefSeq, Sep 2016]","start":39051998,"end":39096671,"strand":1,"description":"WD repeat domain 48 [Source:HGNC Symbol;Acc:HGNC:30914]"}, {"versioned_ensembl_gene_id":"ENSG00000251636.1","gene_symbol":"LINC01218","gene_name":"long intergenic non-protein coding RNA 1218 [Source:HGNC Symbol;Acc:HGNC:41420]","synonyms":"EMCN-IT1","biotype":"sense_intronic","ncbi_id":"107986233","summary":null,"start":100812255,"end":100814280,"strand":-1,"description":"long intergenic non-protein coding RNA 1218 [Source:HGNC Symbol;Acc:HGNC:41420]"}, {"versioned_ensembl_gene_id":"ENSG00000121210.15","gene_symbol":"TMEM131L","gene_name":"transmembrane 131 like [Source:HGNC Symbol;Acc:HGNC:29146]","synonyms":"KIAA0922,DKFZp586H1322","biotype":"protein_coding","ncbi_id":"23240","summary":null,"start":153466346,"end":153636711,"strand":1,"description":"transmembrane 131 like [Source:HGNC Symbol;Acc:HGNC:29146]"}, {"versioned_ensembl_gene_id":"ENSG00000204947.8","gene_symbol":"ZNF425","gene_name":"zinc finger protein 425 [Source:HGNC Symbol;Acc:HGNC:20690]","synonyms":null,"biotype":"protein_coding","ncbi_id":"155054","summary":null,"start":149102784,"end":149126346,"strand":-1,"description":"zinc finger protein 425 [Source:HGNC Symbol;Acc:HGNC:20690]"}, {"versioned_ensembl_gene_id":"ENSG00000251219.1","gene_symbol":"LINC01217","gene_name":"long intergenic non-protein coding RNA 1217 [Source:HGNC Symbol;Acc:HGNC:41419]","synonyms":"EMCN-IT2","biotype":"sense_intronic","ncbi_id":"100874276","summary":null,"start":100778582,"end":100791235,"strand":-1,"description":"long intergenic non-protein coding RNA 1217 [Source:HGNC Symbol;Acc:HGNC:41419]"}, {"versioned_ensembl_gene_id":"ENSG00000254503.1","gene_symbol":"AC010319.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17417031,"end":17418288,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269053.1","gene_symbol":"AC010319.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17419305,"end":17419774,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000141971.12","gene_symbol":"MVB12A","gene_name":"multivesicular body subunit 12A [Source:HGNC Symbol;Acc:HGNC:25153]","synonyms":"FLJ32495,FAM125A","biotype":"protein_coding","ncbi_id":"93343","summary":null,"start":17405722,"end":17433724,"strand":1,"description":"multivesicular body subunit 12A [Source:HGNC Symbol;Acc:HGNC:25153]"}, {"versioned_ensembl_gene_id":"ENSG00000259394.2","gene_symbol":"AC079328.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62953173,"end":62954124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282661.1","gene_symbol":"AC246817.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2712008,"end":2793124,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171433.11","gene_symbol":"GLOD5","gene_name":"glyoxalase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:33358]","synonyms":null,"biotype":"protein_coding","ncbi_id":"392465","summary":"This gene encodes a protein with a glyoxalase domain. [provided by RefSeq, Sep 2011]","start":48761750,"end":48773648,"strand":1,"description":"glyoxalase domain containing 5 [Source:HGNC Symbol;Acc:HGNC:33358]"}, {"versioned_ensembl_gene_id":"ENSG00000281980.1","gene_symbol":"AC246817.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2649201,"end":2651108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197122.11","gene_symbol":"SRC","gene_name":"SRC proto-oncogene, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11283]","synonyms":"SRC1,c-src,ASV","biotype":"protein_coding","ncbi_id":"6714","summary":"This gene is highly similar to the v-src gene of Rous sarcoma virus. This proto-oncogene may play a role in the regulation of embryonic development and cell growth. The protein encoded by this gene is a tyrosine-protein kinase whose activity can be inhibited by phosphorylation by c-SRC kinase. Mutations in this gene could be involved in the malignant progression of colon cancer. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":37344685,"end":37406050,"strand":1,"description":"SRC proto-oncogene, non-receptor tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:11283]"}, {"versioned_ensembl_gene_id":"ENSG00000282435.1","gene_symbol":"AC246817.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2650769,"end":2713141,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175920.16","gene_symbol":"DOK7","gene_name":"docking protein 7 [Source:HGNC Symbol;Acc:HGNC:26594]","synonyms":"FLJ33718,Dok-7,C4orf25,FLJ39137","biotype":"protein_coding","ncbi_id":"285489","summary":"The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","start":3463311,"end":3494483,"strand":1,"description":"docking protein 7 [Source:HGNC Symbol;Acc:HGNC:26594]"}, {"versioned_ensembl_gene_id":"ENSG00000248907.1","gene_symbol":"MTND2P33","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42134]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100873236","summary":null,"start":155461633,"end":155462663,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:42134]"}, {"versioned_ensembl_gene_id":"ENSG00000251407.1","gene_symbol":"MTND1P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42093]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100287591","summary":null,"start":155462873,"end":155463823,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42093]"}, {"versioned_ensembl_gene_id":"ENSG00000237687.2","gene_symbol":"LINC00686","gene_name":"long intergenic non-protein coding RNA 686 [Source:HGNC Symbol;Acc:HGNC:16221]","synonyms":"C20orf90,bA93B14.2","biotype":"lincRNA","ncbi_id":"140865","summary":null,"start":62695024,"end":62700480,"strand":-1,"description":"long intergenic non-protein coding RNA 686 [Source:HGNC Symbol;Acc:HGNC:16221]"}, {"versioned_ensembl_gene_id":"ENSG00000224621.1","gene_symbol":"AL451042.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16159266,"end":16161883,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251244.1","gene_symbol":"AC107208.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":155515727,"end":155517459,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101188.4","gene_symbol":"NTSR1","gene_name":"neurotensin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8039]","synonyms":"NTR","biotype":"protein_coding","ncbi_id":"4923","summary":"Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secretion. [provided by RefSeq, Jul 2008]","start":62708837,"end":62762771,"strand":1,"description":"neurotensin receptor 1 [Source:HGNC Symbol;Acc:HGNC:8039]"}, {"versioned_ensembl_gene_id":"ENSG00000276799.2","gene_symbol":"WNT9B","gene_name":"Wnt family member 9B [Source:HGNC Symbol;Acc:HGNC:12779]","synonyms":"WNT15,WNT14B","biotype":"protein_coding","ncbi_id":"7484","summary":"The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. Study of its expression in the teratocarcinoma cell line NT2 suggests that it may be implicated in the early process of neuronal differentiation of NT2 cells induced by retinoic acid. This gene is clustered with WNT3, another family member, in the chromosome 17q21 region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":46662121,"end":46715644,"strand":1,"description":"Wnt family member 9B [Source:HGNC Symbol;Acc:HGNC:12779]"}, {"versioned_ensembl_gene_id":"ENSG00000126003.6","gene_symbol":"PLAGL2","gene_name":"PLAG1 like zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:9047]","synonyms":"ZNF900","biotype":"protein_coding","ncbi_id":"5326","summary":" Pleiomorphic adenoma gene-like 2 is a zinc-finger protein that recognizes DNA and/or RNA. [provided by RefSeq, Jul 2008]","start":32192503,"end":32207791,"strand":-1,"description":"PLAG1 like zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:9047]"}, {"versioned_ensembl_gene_id":"ENSG00000234853.2","gene_symbol":"NDUFA5P3","gene_name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48845]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288035","summary":null,"start":19383217,"end":19383887,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48845]"}, {"versioned_ensembl_gene_id":"ENSG00000177076.5","gene_symbol":"ACER2","gene_name":"alkaline ceramidase 2 [Source:HGNC Symbol;Acc:HGNC:23675]","synonyms":"FLJ41587,ASAH3L,ALKCDase2","biotype":"protein_coding","ncbi_id":"340485","summary":"The sphingolipid metabolite sphingosine-1-phosphate promotes cell proliferation and survival, whereas its precursor, sphingosine, has the opposite effect. The ceramidase ACER2 hydrolyzes very long chain ceramides to generate sphingosine (Xu et al., 2006 [PubMed 16940153]).[supplied by OMIM, Jul 2010]","start":19409059,"end":19452020,"strand":1,"description":"alkaline ceramidase 2 [Source:HGNC Symbol;Acc:HGNC:23675]"}, {"versioned_ensembl_gene_id":"ENSG00000227557.1","gene_symbol":"MTND3P9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42149]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873184","summary":null,"start":143098484,"end":143098829,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42149]"}, {"versioned_ensembl_gene_id":"ENSG00000284167.1","gene_symbol":"AC013437.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":143099936,"end":143100612,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283199.1","gene_symbol":"FP565324.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":113953705,"end":113973997,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236300.2","gene_symbol":"MTND4LP12","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42246]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075239","summary":null,"start":143098123,"end":143098417,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:42246]"}, {"versioned_ensembl_gene_id":"ENSG00000223669.1","gene_symbol":"AL357033.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":62732566,"end":62735347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232772.1","gene_symbol":"MTND4P22","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42209]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873244","summary":null,"start":143096839,"end":143098007,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:42209]"}, {"versioned_ensembl_gene_id":"ENSG00000224288.2","gene_symbol":"MTCYBP11","gene_name":"mitochondrially encoded cytochrome b pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51962]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075122","summary":null,"start":143093056,"end":143094164,"strand":-1,"description":"mitochondrially encoded cytochrome b pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51962]"}, {"versioned_ensembl_gene_id":"ENSG00000225476.1","gene_symbol":"MTCO3P5","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52123]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075228","summary":null,"start":143098898,"end":143099933,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52123]"}, {"versioned_ensembl_gene_id":"ENSG00000228655.6","gene_symbol":"AC096558.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143295421,"end":143480789,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244668.1","gene_symbol":"SNRPCP3","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128469","summary":null,"start":150719997,"end":150720836,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:49818]"}, {"versioned_ensembl_gene_id":"ENSG00000168412.6","gene_symbol":"MTNR1A","gene_name":"melatonin receptor 1A [Source:HGNC Symbol;Acc:HGNC:7463]","synonyms":"MEL-1A-R","biotype":"protein_coding","ncbi_id":"4543","summary":"This gene encodes one of two high affinity forms of a receptor for melatonin, the primary hormone secreted by the pineal gland. This receptor is a G-protein coupled, 7-transmembrane receptor that is responsible for melatonin effects on mammalian circadian rhythm and reproductive alterations affected by day length. The receptor is an integral membrane protein that is readily detectable and localized to two specific regions of the brain. The hypothalamic suprachiasmatic nucleus appears to be involved in circadian rhythm while the hypophysial pars tuberalis may be responsible for the reproductive effects of melatonin. [provided by RefSeq, Jul 2008]","start":186533655,"end":186555567,"strand":-1,"description":"melatonin receptor 1A [Source:HGNC Symbol;Acc:HGNC:7463]"}, {"versioned_ensembl_gene_id":"ENSG00000240137.5","gene_symbol":"ERICH6-AS1","gene_name":"ERICH6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41205]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101928085","summary":null,"start":150703564,"end":150720146,"strand":1,"description":"ERICH6 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41205]"}, {"versioned_ensembl_gene_id":"ENSG00000128165.8","gene_symbol":"ADM2","gene_name":"adrenomedullin 2 [Source:HGNC Symbol;Acc:HGNC:28898]","synonyms":"AM2,FLJ21135","biotype":"protein_coding","ncbi_id":"79924","summary":"This gene encodes a member of the calcitonin gene-related peptide (CGRP)/calcitonin family of hormones that play a role in the regulation of cardiovascular homeostasis, prolactin release, anti-diuresis, anti-natriuresis, and regulation of food and water intake. The encoded protein is proteolytically processed to generate one or more biologically active peptides. [provided by RefSeq, Jul 2015]","start":50481556,"end":50486440,"strand":1,"description":"adrenomedullin 2 [Source:HGNC Symbol;Acc:HGNC:28898]"}, {"versioned_ensembl_gene_id":"ENSG00000113805.8","gene_symbol":"CNTN3","gene_name":"contactin 3 [Source:HGNC Symbol;Acc:HGNC:2173]","synonyms":"PANG,BIG-1","biotype":"protein_coding","ncbi_id":"5067","summary":null,"start":74262568,"end":74521140,"strand":-1,"description":"contactin 3 [Source:HGNC Symbol;Acc:HGNC:2173]"}, {"versioned_ensembl_gene_id":"ENSG00000281382.1","gene_symbol":"AC236970.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41531206,"end":41532026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257226.1","gene_symbol":"AC079584.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143766620,"end":143776073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234166.1","gene_symbol":"ARHGEF19-AS1","gene_name":"ARHGEF19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39996]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874233","summary":null,"start":16197854,"end":16198357,"strand":1,"description":"ARHGEF19 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39996]"}, {"versioned_ensembl_gene_id":"ENSG00000176834.13","gene_symbol":"VSIG10","gene_name":"V-set and immunoglobulin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:26078]","synonyms":null,"biotype":"protein_coding","ncbi_id":"54621","summary":null,"start":118063593,"end":118136026,"strand":-1,"description":"V-set and immunoglobulin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:26078]"}, {"versioned_ensembl_gene_id":"ENSG00000231758.2","gene_symbol":"AC092652.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143640756,"end":143656179,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142632.16","gene_symbol":"ARHGEF19","gene_name":"Rho guanine nucleotide exchange factor 19 [Source:HGNC Symbol;Acc:HGNC:26604]","synonyms":"WGEF,FLJ33962","biotype":"protein_coding","ncbi_id":"128272","summary":"Guanine nucleotide exchange factors (GEFs) such as ARHGEF19 accelerate the GTPase activity of Rho GTPases (see RHOA, MIM 165390).[supplied by OMIM, Dec 2008]","start":16197854,"end":16212609,"strand":-1,"description":"Rho guanine nucleotide exchange factor 19 [Source:HGNC Symbol;Acc:HGNC:26604]"}, {"versioned_ensembl_gene_id":"ENSG00000149922.10","gene_symbol":"TBX6","gene_name":"T-box 6 [Source:HGNC Symbol;Acc:HGNC:11605]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6911","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Knockout studies in mice indicate that this gene is important for specification of paraxial mesoderm structures. [provided by RefSeq, Aug 2008]","start":30085793,"end":30091887,"strand":-1,"description":"T-box 6 [Source:HGNC Symbol;Acc:HGNC:11605]"}, {"versioned_ensembl_gene_id":"ENSG00000271851.1","gene_symbol":"AC087501.5","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9553323,"end":9555696,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258268.1","gene_symbol":"AC079793.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143518867,"end":143598002,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251165.5","gene_symbol":"F11-AS1","gene_name":"F11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27725]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"285441","summary":null,"start":186286094,"end":186500997,"strand":-1,"description":"F11 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27725]"}, {"versioned_ensembl_gene_id":"ENSG00000263051.1","gene_symbol":"AC087501.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9547298,"end":9548541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075884.13","gene_symbol":"ARHGAP15","gene_name":"Rho GTPase activating protein 15 [Source:HGNC Symbol;Acc:HGNC:21030]","synonyms":"BM046","biotype":"protein_coding","ncbi_id":"55843","summary":"RHO GTPases (see ARHA; MIM 165390) regulate diverse biologic processes, and their activity is regulated by RHO GTPase-activating proteins (GAPs), such as ARHGAP15 (Seoh et al., 2003 [PubMed 12650940]).[supplied by OMIM, Mar 2008]","start":143091362,"end":143768352,"strand":1,"description":"Rho GTPase activating protein 15 [Source:HGNC Symbol;Acc:HGNC:21030]"}, {"versioned_ensembl_gene_id":"ENSG00000181789.14","gene_symbol":"COPG1","gene_name":"coatomer protein complex subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:2236]","synonyms":"COPG","biotype":"protein_coding","ncbi_id":"22820","summary":null,"start":129249606,"end":129277773,"strand":1,"description":"coatomer protein complex subunit gamma 1 [Source:HGNC Symbol;Acc:HGNC:2236]"}, {"versioned_ensembl_gene_id":"ENSG00000170310.14","gene_symbol":"STX8","gene_name":"syntaxin 8 [Source:HGNC Symbol;Acc:HGNC:11443]","synonyms":"CARB","biotype":"protein_coding","ncbi_id":"9482","summary":"The gene is a member of the syntaxin family. The encoded protein is involved in protein trafficking from early to late endosomes via vesicle fusion and exocytosis. A related pseudogene has been identified on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":9250471,"end":9576591,"strand":-1,"description":"syntaxin 8 [Source:HGNC Symbol;Acc:HGNC:11443]"}, {"versioned_ensembl_gene_id":"ENSG00000232563.1","gene_symbol":"CRB3P1","gene_name":"crumbs cell polarity complex component 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49684]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480279","summary":null,"start":1394173,"end":1394448,"strand":-1,"description":"crumbs cell polarity complex component 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49684]"}, {"versioned_ensembl_gene_id":"ENSG00000262510.2","gene_symbol":"LINC00308","gene_name":"long intergenic non-protein coding RNA 308 [Source:NCBI gene;Acc:54143]","synonyms":"PRED16,NCRNA00308,C21orf74,PRED16,NCRNA00308,C21orf74","biotype":"lincRNA","ncbi_id":"54143","summary":null,"start":22109451,"end":22116528,"strand":1,"description":"long intergenic non-protein coding RNA 308 [Source:NCBI gene;Acc:54143]"}, {"versioned_ensembl_gene_id":"ENSG00000261441.1","gene_symbol":"AC124068.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":89335053,"end":89336161,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101346.13","gene_symbol":"POFUT1","gene_name":"protein O-fucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:14988]","synonyms":"FUT12,O-FUT,O-Fuc-T,KIAA0180","biotype":"protein_coding","ncbi_id":"23509","summary":"This gene encodes a member of the glycosyltransferase O-Fuc family. This enzyme adds O-fucose through an O-glycosidic linkage to conserved serine or threonine residues in the epidermal growth factor-like repeats of a number of cell surface and secreted proteins. O-fucose glycans are involved in ligand-induced receptor signaling. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":32207880,"end":32238667,"strand":1,"description":"protein O-fucosyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:14988]"}, {"versioned_ensembl_gene_id":"ENSG00000231909.7","gene_symbol":"MAP1LC3BP1","gene_name":"microtubule associated protein 1 light chain 3 beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49783]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"392288","summary":null,"start":19460926,"end":19464524,"strand":-1,"description":"microtubule associated protein 1 light chain 3 beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49783]"}, {"versioned_ensembl_gene_id":"ENSG00000134769.21","gene_symbol":"DTNA","gene_name":"dystrobrevin alpha [Source:HGNC Symbol;Acc:HGNC:3057]","synonyms":"DTN-3,DTN-2,DTN-1,DTN,DRP3,D18S892E","biotype":"protein_coding","ncbi_id":"1837","summary":"The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":34493290,"end":34891844,"strand":1,"description":"dystrobrevin alpha [Source:HGNC Symbol;Acc:HGNC:3057]"}, {"versioned_ensembl_gene_id":"ENSG00000261643.1","gene_symbol":"AL590235.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3503597,"end":3504457,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277373.1","gene_symbol":"AL132765.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":17565501,"end":17565851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257084.1","gene_symbol":"MIR200CHG","gene_name":"MIR200C and MIR141 host gene [Source:HGNC Symbol;Acc:HGNC:53161]","synonyms":"U47924.27","biotype":"lincRNA","ncbi_id":"105369635","summary":null,"start":6963246,"end":6964447,"strand":1,"description":"MIR200C and MIR141 host gene [Source:HGNC Symbol;Acc:HGNC:53161]"}, {"versioned_ensembl_gene_id":"ENSG00000125864.13","gene_symbol":"BFSP1","gene_name":"beaded filament structural protein 1 [Source:HGNC Symbol;Acc:HGNC:1040]","synonyms":"LIFL-H,filensin,CP94,CP115","biotype":"protein_coding","ncbi_id":"631","summary":"This gene encodes a lens-specific intermediate filament-like protein named filensin. The encoded protein is expressed in lens fiber cells after differentiation has begun. This protein functions as a component of the beaded filament which is a cytoskeletal structure found in lens fiber cells. Mutations in this gene are the cause of autosomal recessive cortical juvenile-onset cataract. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":17493905,"end":17569220,"strand":-1,"description":"beaded filament structural protein 1 [Source:HGNC Symbol;Acc:HGNC:1040]"}, {"versioned_ensembl_gene_id":"ENSG00000272297.2","gene_symbol":"AC018709.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":186426546,"end":186555328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163956.10","gene_symbol":"LRPAP1","gene_name":"LDL receptor related protein associated protein 1 [Source:HGNC Symbol;Acc:HGNC:6701]","synonyms":"RAP,HBP44,A2MRAP","biotype":"protein_coding","ncbi_id":"4043","summary":"This gene encodes a protein that interacts with the low density lipoprotein (LDL) receptor-related protein and facilitates its proper folding and localization by preventing the binding of ligands. Mutations in this gene have been identified in individuals with myopia 23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]","start":3506376,"end":3532559,"strand":-1,"description":"LDL receptor related protein associated protein 1 [Source:HGNC Symbol;Acc:HGNC:6701]"}, {"versioned_ensembl_gene_id":"ENSG00000213332.4","gene_symbol":"SLC25A5P6","gene_name":"solute carrier family 25 member 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:512]","synonyms":"ANTP6","biotype":"processed_pseudogene","ncbi_id":"644042","summary":null,"start":186328716,"end":186329601,"strand":-1,"description":"solute carrier family 25 member 5 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:512]"}, {"versioned_ensembl_gene_id":"ENSG00000185808.13","gene_symbol":"PIGP","gene_name":"phosphatidylinositol glycan anchor biosynthesis class P [Source:HGNC Symbol;Acc:HGNC:3046]","synonyms":"DSRC,DSCR5,DCRC","biotype":"protein_coding","ncbi_id":"51227","summary":"This gene encodes an enzyme involved in the first step of glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface. The encoded protein is a component of the GPI-N-acetylglucosaminyltransferase complex that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI). This gene is located in the Down Syndrome critical region on chromosome 21 and is a candidate for the pathogenesis of Down syndrome. This gene has multiple pseudogenes and is a member of the phosphatidylinositol glycan anchor biosynthesis gene family. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Feb 2016]","start":37059170,"end":37073170,"strand":-1,"description":"phosphatidylinositol glycan anchor biosynthesis class P [Source:HGNC Symbol;Acc:HGNC:3046]"}, {"versioned_ensembl_gene_id":"ENSG00000274513.4","gene_symbol":"LILRB2","gene_name":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]","synonyms":"MIR10,ILT4,MIR-10,CD85d,LIR2,LIR-2","biotype":"protein_coding","ncbi_id":"10288","summary":"This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":54274450,"end":54281944,"strand":-1,"description":"leukocyte immunoglobulin like receptor B2 [Source:HGNC Symbol;Acc:HGNC:6606]"}, {"versioned_ensembl_gene_id":"ENSG00000241547.1","gene_symbol":"ACTG1P20","gene_name":"actin gamma 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51500]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644961","summary":null,"start":27325329,"end":27325796,"strand":1,"description":"actin gamma 1 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:51500]"}, {"versioned_ensembl_gene_id":"ENSG00000224949.2","gene_symbol":"AL589872.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":54147372,"end":54147659,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234260.1","gene_symbol":"HLA-DPA2","gene_name":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]","synonyms":"HLA-DP2A","biotype":"unprocessed_pseudogene","ncbi_id":"646702","summary":null,"start":33130812,"end":33136354,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4939]"}, {"versioned_ensembl_gene_id":"ENSG00000184083.11","gene_symbol":"FAM120C","gene_name":"family with sequence similarity 120C [Source:HGNC Symbol;Acc:HGNC:16949]","synonyms":"FLJ20506,CXorf17,ORF34","biotype":"protein_coding","ncbi_id":"54954","summary":"This gene encodes a potential transmembrane protein and lies in a region where mutations and deletions have been associated with intellectual disability and autism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":54068324,"end":54183281,"strand":-1,"description":"family with sequence similarity 120C [Source:HGNC Symbol;Acc:HGNC:16949]"}, {"versioned_ensembl_gene_id":"ENSG00000259705.1","gene_symbol":"AC084757.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48645951,"end":48652016,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273993.4","gene_symbol":"PTPRK","gene_name":"protein tyrosine phosphatase, receptor type K [Source:HGNC Symbol;Acc:HGNC:9674]","synonyms":"R-PTP-kappa","biotype":"protein_coding","ncbi_id":"5796","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP mu (MAM) domain, an Ig-like domain and four fibronectin type III-like repeats. This PTP was shown to mediate homophilic intercellular interaction, possibly through the interaction with beta- and gamma-catenin at adherens junctions. Expression of this gene was found to be stimulated by TGF-beta 1, which may be important for the inhibition of keratinocyte proliferation. [provided by RefSeq, Jul 2008]","start":127968779,"end":128524810,"strand":-1,"description":"protein tyrosine phosphatase, receptor type K [Source:HGNC Symbol;Acc:HGNC:9674]"}, {"versioned_ensembl_gene_id":"ENSG00000225408.1","gene_symbol":"AL136980.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5719021,"end":5720244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000101189.6","gene_symbol":"MRGBP","gene_name":"MRG domain binding protein [Source:HGNC Symbol;Acc:HGNC:15866]","synonyms":"MRG15BP,FLJ10914,Eaf7,C20orf20","biotype":"protein_coding","ncbi_id":"55257","summary":null,"start":62796453,"end":62801738,"strand":1,"description":"MRG domain binding protein [Source:HGNC Symbol;Acc:HGNC:15866]"}, {"versioned_ensembl_gene_id":"ENSG00000089220.4","gene_symbol":"PEBP1","gene_name":"phosphatidylethanolamine binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8630]","synonyms":"RKIP,PEBP,PBP,HCNP","biotype":"protein_coding","ncbi_id":"5037","summary":"This gene encodes a member of the phosphatidylethanolamine-binding family of proteins and has been shown to modulate multiple signaling pathways, including the MAP kinase (MAPK), NF-kappa B, and glycogen synthase kinase-3 (GSK-3) signaling pathways. The encoded protein can be further processed to form a smaller cleavage product, hippocampal cholinergic neurostimulating peptide (HCNP), which may be involved in neural development. This gene has been implicated in numerous human cancers and may act as a metastasis suppressor gene. Multiple pseudogenes of this gene have been identified in the genome. [provided by RefSeq, Jul 2015]","start":118135858,"end":118145584,"strand":1,"description":"phosphatidylethanolamine binding protein 1 [Source:HGNC Symbol;Acc:HGNC:8630]"}, {"versioned_ensembl_gene_id":"ENSG00000236040.1","gene_symbol":"CHIAP1","gene_name":"chitinase, acidic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44462]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420342","summary":null,"start":111250254,"end":111256715,"strand":1,"description":"chitinase, acidic pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44462]"}, {"versioned_ensembl_gene_id":"ENSG00000184900.15","gene_symbol":"SUMO3","gene_name":"small ubiquitin-like modifier 3 [Source:HGNC Symbol;Acc:HGNC:11124]","synonyms":"SMT3H1,SMT3A","biotype":"protein_coding","ncbi_id":"6612","summary":"This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins. The encoded protein is covalently conjugated to other proteins via a post-translation modification known as sumoylation. Sumoylation may play a role in a wide variety of cellular processes, including nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and signal transduction. Alternatively spliced transcript variants encoding distinct proteins have been described. [provided by RefSeq, Feb 2014]","start":44805617,"end":44818779,"strand":-1,"description":"small ubiquitin-like modifier 3 [Source:HGNC Symbol;Acc:HGNC:11124]"}, {"versioned_ensembl_gene_id":"ENSG00000114745.13","gene_symbol":"GORASP1","gene_name":"golgi reassembly stacking protein 1 [Source:HGNC Symbol;Acc:HGNC:16769]","synonyms":"P65,GRASP65,GOLPH5,FLJ23443","biotype":"protein_coding","ncbi_id":"64689","summary":"The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a membrane protein involved in establishing the stacked structure of the Golgi apparatus. It is a caspase-3 substrate, and cleavage of this encoded protein contributes to Golgi fragmentation in apoptosis. This encoded protein can form a complex with the Golgi matrix protein GOLGA2, and this complex binds to the vesicle docking protein p115. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]","start":39096659,"end":39108363,"strand":-1,"description":"golgi reassembly stacking protein 1 [Source:HGNC Symbol;Acc:HGNC:16769]"}, {"versioned_ensembl_gene_id":"ENSG00000283698.1","gene_symbol":"AC012442.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":null,"summary":null,"start":112439312,"end":112469687,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241022.1","gene_symbol":"NIPA2P2","gene_name":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42042]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130204","summary":null,"start":75084155,"end":75085237,"strand":1,"description":"non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:42042]"}, {"versioned_ensembl_gene_id":"ENSG00000237986.3","gene_symbol":"CELF2-AS2","gene_name":"CELF2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44703]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"439950","summary":null,"start":11071541,"end":11105504,"strand":-1,"description":"CELF2 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:44703]"}, {"versioned_ensembl_gene_id":"ENSG00000050730.15","gene_symbol":"TNIP3","gene_name":"TNFAIP3 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:19315]","synonyms":"LIND,FLJ21162,ABIN-3","biotype":"protein_coding","ncbi_id":"79931","summary":null,"start":121131408,"end":121227466,"strand":-1,"description":"TNFAIP3 interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:19315]"}, {"versioned_ensembl_gene_id":"ENSG00000232487.1","gene_symbol":"RASA3-IT1","gene_name":"RASA3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39938]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874321","summary":null,"start":114107569,"end":114108820,"strand":-1,"description":"RASA3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39938]"}, {"versioned_ensembl_gene_id":"ENSG00000185989.10","gene_symbol":"RASA3","gene_name":"RAS p21 protein activator 3 [Source:HGNC Symbol;Acc:HGNC:20331]","synonyms":"GAPIII,GAP1IP4BP","biotype":"protein_coding","ncbi_id":"22821","summary":"This gene encodes a protein that binds inositol 1,3,4,5-tetrakisphosphate and stimulates the GTPase activity of Ras p21. This protein functions as a negative regulator of the Ras signalling pathway. It is localized to the cell membrane via a pleckstrin homology (PH) domain in the C-terminal region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":113977783,"end":114132611,"strand":-1,"description":"RAS p21 protein activator 3 [Source:HGNC Symbol;Acc:HGNC:20331]"}, {"versioned_ensembl_gene_id":"ENSG00000229206.3","gene_symbol":"AL162408.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11030334,"end":11030868,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181800.5","gene_symbol":"CELF2-AS1","gene_name":"CELF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23515]","synonyms":"FLJ40494,Em:AC026887.2,C10orf31","biotype":"antisense_RNA","ncbi_id":"414196","summary":null,"start":11316834,"end":11319884,"strand":-1,"description":"CELF2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:23515]"}, {"versioned_ensembl_gene_id":"ENSG00000231496.1","gene_symbol":"AL136369.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10960151,"end":10970816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282230.1","gene_symbol":"ADAM9","gene_name":"ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:HGNC:216]","synonyms":"Mltng,MDC9,MCMP,KIAA0021,CORD9","biotype":"protein_coding","ncbi_id":"8754","summary":"This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene interacts with SH3 domain-containing proteins, binds mitotic arrest deficient 2 beta protein, and is also involved in TPA-induced ectodomain shedding of membrane-anchored heparin-binding EGF-like growth factor. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2010]","start":39101863,"end":39105144,"strand":1,"description":"ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:HGNC:216]"}, {"versioned_ensembl_gene_id":"ENSG00000274859.1","gene_symbol":"AC131238.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":118066398,"end":118066725,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228705.1","gene_symbol":"LINC00659","gene_name":"long intergenic non-protein coding RNA 659 [Source:HGNC Symbol;Acc:HGNC:44316]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100652730","summary":null,"start":62774128,"end":62775412,"strand":-1,"description":"long intergenic non-protein coding RNA 659 [Source:HGNC Symbol;Acc:HGNC:44316]"}, {"versioned_ensembl_gene_id":"ENSG00000048740.18","gene_symbol":"CELF2","gene_name":"CUGBP Elav-like family member 2 [Source:HGNC Symbol;Acc:HGNC:2550]","synonyms":"NAPOR-2,Etr-3,CUGBP2,BRUNOL3","biotype":"protein_coding","ncbi_id":"10659","summary":"Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":10798397,"end":11336675,"strand":1,"description":"CUGBP Elav-like family member 2 [Source:HGNC Symbol;Acc:HGNC:2550]"}, {"versioned_ensembl_gene_id":"ENSG00000225751.2","gene_symbol":"AC087501.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9452197,"end":9470014,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135643.4","gene_symbol":"KCNMB4","gene_name":"potassium calcium-activated channel subfamily M regulatory beta subunit 4 [Source:HGNC Symbol;Acc:HGNC:6289]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27345","summary":"MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit and the modulatory beta subunit. The protein encoded by this gene is an auxiliary beta subunit which slows activation kinetics, leads to steeper calcium sensitivity, and shifts the voltage range of current activation to more negative potentials than does the beta 1 subunit. [provided by RefSeq, Jul 2008]","start":70366276,"end":70434292,"strand":1,"description":"potassium calcium-activated channel subfamily M regulatory beta subunit 4 [Source:HGNC Symbol;Acc:HGNC:6289]"}, {"versioned_ensembl_gene_id":"ENSG00000263708.2","gene_symbol":"AC005695.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9283174,"end":9305651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000107036.11","gene_symbol":"RIC1","gene_name":"RIC1 homolog, RAB6A GEF complex partner 1 [Source:HGNC Symbol;Acc:HGNC:17686]","synonyms":"KIAA1432,bA207C16.1","biotype":"protein_coding","ncbi_id":"57589","summary":null,"start":5629025,"end":5776557,"strand":1,"description":"RIC1 homolog, RAB6A GEF complex partner 1 [Source:HGNC Symbol;Acc:HGNC:17686]"}, {"versioned_ensembl_gene_id":"ENSG00000248574.1","gene_symbol":"ADAM20P2","gene_name":"ADAM metallopeptidase domain 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43901]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100533671","summary":null,"start":175574868,"end":175576140,"strand":1,"description":"ADAM metallopeptidase domain 20 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43901]"}, {"versioned_ensembl_gene_id":"ENSG00000137252.9","gene_symbol":"HCRTR2","gene_name":"hypocretin receptor 2 [Source:HGNC Symbol;Acc:HGNC:4849]","synonyms":"OX2R","biotype":"protein_coding","ncbi_id":"3062","summary":"The protein encoded by this gene is a G-protein coupled receptor involved in the regulation of feeding behavior. The encoded protein binds the hypothalamic neuropeptides orexin A and orexin B. A related gene (HCRTR1) encodes a G-protein coupled receptor that selectively binds orexin A. [provided by RefSeq, Jan 2009]","start":55106460,"end":55282620,"strand":1,"description":"hypocretin receptor 2 [Source:HGNC Symbol;Acc:HGNC:4849]"}, {"versioned_ensembl_gene_id":"ENSG00000197024.8","gene_symbol":"ZNF398","gene_name":"zinc finger protein 398 [Source:HGNC Symbol;Acc:HGNC:18373]","synonyms":"ZER6,P71,P51,KIAA1339","biotype":"protein_coding","ncbi_id":"57541","summary":"This gene encodes a member of the Kruppel family of C2H2-type zinc-finger transcription factor proteins. The encoded protein acts as a transcriptional activator. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described, but their full length sequence has not been determined. [provided by RefSeq, Jul 2008]","start":149126416,"end":149182802,"strand":1,"description":"zinc finger protein 398 [Source:HGNC Symbol;Acc:HGNC:18373]"}, {"versioned_ensembl_gene_id":"ENSG00000232158.1","gene_symbol":"C11orf98P1","gene_name":"chromosome 11 open reading frame 98 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480289","summary":null,"start":19705338,"end":19705655,"strand":1,"description":"chromosome 11 open reading frame 98 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49784]"}, {"versioned_ensembl_gene_id":"ENSG00000092470.11","gene_symbol":"WDR76","gene_name":"WD repeat domain 76 [Source:HGNC Symbol;Acc:HGNC:25773]","synonyms":"FLJ12973","biotype":"protein_coding","ncbi_id":"79968","summary":null,"start":43826963,"end":43868419,"strand":1,"description":"WD repeat domain 76 [Source:HGNC Symbol;Acc:HGNC:25773]"}, {"versioned_ensembl_gene_id":"ENSG00000283267.1","gene_symbol":"FAM237B","gene_name":"family with sequence similarity 237 member B [Source:HGNC Symbol;Acc:HGNC:53217]","synonyms":null,"biotype":"protein_coding","ncbi_id":"107986818","summary":null,"start":90316503,"end":90321308,"strand":-1,"description":"family with sequence similarity 237 member B [Source:HGNC Symbol;Acc:HGNC:53217]"}, {"versioned_ensembl_gene_id":"ENSG00000196950.13","gene_symbol":"SLC39A10","gene_name":"solute carrier family 39 member 10 [Source:HGNC Symbol;Acc:HGNC:20861]","synonyms":"KIAA1265,FLJ90515,DKFZp564L2123","biotype":"protein_coding","ncbi_id":"57181","summary":"Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A10 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]","start":195575977,"end":195737702,"strand":1,"description":"solute carrier family 39 member 10 [Source:HGNC Symbol;Acc:HGNC:20861]"}, {"versioned_ensembl_gene_id":"ENSG00000155886.11","gene_symbol":"SLC24A2","gene_name":"solute carrier family 24 member 2 [Source:HGNC Symbol;Acc:HGNC:10976]","synonyms":"NCKX2","biotype":"protein_coding","ncbi_id":"25769","summary":"This gene encodes a member of the calcium/cation antiporter superfamily of transport proteins. The encoded protein belongs to the SLC24 branch of exchangers, which can mediate the extrusion of one Ca2+ ion and one K+ ion in exchange for four Na+ ions. This family member is a retinal cone/brain exchanger that can mediate a light-induced decrease in free Ca2+ concentration. This protein may also play a neuroprotective role during ischemic brain injury. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]","start":19507452,"end":19786928,"strand":-1,"description":"solute carrier family 24 member 2 [Source:HGNC Symbol;Acc:HGNC:10976]"}, {"versioned_ensembl_gene_id":"ENSG00000225498.1","gene_symbol":"AC002064.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":90312496,"end":90322592,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235329.2","gene_symbol":"AL031183.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113347413,"end":113347619,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000060491.16","gene_symbol":"OGFR","gene_name":"opioid growth factor receptor [Source:HGNC Symbol;Acc:HGNC:15768]","synonyms":"7-60","biotype":"protein_coding","ncbi_id":"11054","summary":"The protein encoded by this gene is a receptor for opioid growth factor (OGF), also known as [Met(5)]-enkephalin. OGF is a negative regulator of cell proliferation and tissue organization in a variety of processes. The encoded unbound receptor for OGF has been localized to the outer nuclear envelope, where it binds OGF and is translocated into the nucleus. The coding sequence of this gene contains a polymorphic region of 60 nt tandem imperfect repeat units. Several transcripts containing between zero and eight repeat units have been reported. [provided by RefSeq, Jul 2008]","start":62804835,"end":62814000,"strand":1,"description":"opioid growth factor receptor [Source:HGNC Symbol;Acc:HGNC:15768]"}, {"versioned_ensembl_gene_id":"ENSG00000183520.11","gene_symbol":"UTP11","gene_name":"UTP11, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24329]","synonyms":"UTP11L,CGI-94","biotype":"protein_coding","ncbi_id":"51118","summary":null,"start":38009258,"end":38024824,"strand":1,"description":"UTP11, small subunit processome component [Source:HGNC Symbol;Acc:HGNC:24329]"}, {"versioned_ensembl_gene_id":"ENSG00000273925.1","gene_symbol":"AC084757.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48662531,"end":48663056,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227577.1","gene_symbol":"COL11A2P1","gene_name":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]","synonyms":"COL11A2P,cD0826Q1.1","biotype":"unprocessed_pseudogene","ncbi_id":"394214","summary":null,"start":33142826,"end":33146362,"strand":-1,"description":"collagen type XI alpha 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13947]"}, {"versioned_ensembl_gene_id":"ENSG00000274857.2","gene_symbol":"PLEKHA3P1","gene_name":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]","synonyms":"PLEKHA3P","biotype":"processed_pseudogene","ncbi_id":"91405","summary":null,"start":41521043,"end":41521989,"strand":-1,"description":"pleckstrin homology domain containing A3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:19648]"}, {"versioned_ensembl_gene_id":"ENSG00000276944.2","gene_symbol":"AC243960.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41506152,"end":41506898,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226071.9","gene_symbol":"HLA-DPB2","gene_name":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]","synonyms":"DPB2,DP2B,HLA-DP2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"3116","summary":null,"start":33151483,"end":33168112,"strand":1,"description":"major histocompatibility complex, class II, DP beta 2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:4941]"}, {"versioned_ensembl_gene_id":"ENSG00000257284.1","gene_symbol":"AC013437.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143162078,"end":143172172,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224613.6","gene_symbol":"AC095032.1","gene_name":null,"synonyms":null,"biotype":"bidirectional_promoter_lncRNA","ncbi_id":null,"summary":null,"start":103418079,"end":103525483,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226839.1","gene_symbol":"MTND6P11","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39474]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480727","summary":null,"start":143094233,"end":143094715,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:39474]"}, {"versioned_ensembl_gene_id":"ENSG00000257277.1","gene_symbol":"AC092652.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143676165,"end":143741294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283563.1","gene_symbol":"AC098650.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":28349178,"end":29767537,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235593.1","gene_symbol":"RBMS3-AS1","gene_name":"RBMS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39987]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873977","summary":null,"start":29926811,"end":29934156,"strand":-1,"description":"RBMS3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39987]"}, {"versioned_ensembl_gene_id":"ENSG00000283994.1","gene_symbol":"AC092652.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":143601517,"end":143608759,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215004.3","gene_symbol":"MESTP4","gene_name":"mesoderm specific transcript pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38554]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"131572","summary":null,"start":29087396,"end":29088599,"strand":1,"description":"mesoderm specific transcript pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:38554]"}, {"versioned_ensembl_gene_id":"ENSG00000196711.8","gene_symbol":"ALKAL1","gene_name":"ALK and LTK ligand 1 [Source:HGNC Symbol;Acc:HGNC:33775]","synonyms":"AUGB,UNQ9433,FAM150A","biotype":"protein_coding","ncbi_id":"389658","summary":null,"start":52534037,"end":52565507,"strand":-1,"description":"ALK and LTK ligand 1 [Source:HGNC Symbol;Acc:HGNC:33775]"}, {"versioned_ensembl_gene_id":"ENSG00000231766.1","gene_symbol":"MTCO2P5","gene_name":"mitochondrially encoded cytochrome c oxidase II pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52124]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075181","summary":null,"start":143100930,"end":143101355,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase II pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:52124]"}, {"versioned_ensembl_gene_id":"ENSG00000144642.21","gene_symbol":"RBMS3","gene_name":"RNA binding motif single stranded interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:13427]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27303","summary":"This gene encodes an RNA-binding protein that belongs to the c-myc gene single-strand binding protein family. These proteins are characterized by the presence of two sets of ribonucleoprotein consensus sequence (RNP-CS) that contain conserved motifs, RNP1 and RNP2, originally described in RNA binding proteins, and required for DNA binding. These proteins have been implicated in such diverse functions as DNA replication, gene transcription, cell cycle progression and apoptosis. The encoded protein was isolated by virtue of its binding to an upstream element of the alpha2(I) collagen promoter. The observation that this protein localizes mostly in the cytoplasm suggests that it may be involved in a cytoplasmic function such as controlling RNA metabolism, rather than transcription. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]","start":28574791,"end":30010391,"strand":1,"description":"RNA binding motif single stranded interacting protein 3 [Source:HGNC Symbol;Acc:HGNC:13427]"}, {"versioned_ensembl_gene_id":"ENSG00000230759.1","gene_symbol":"AC095032.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103414879,"end":103425465,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257640.1","gene_symbol":"AC096558.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":143295586,"end":143572105,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253175.1","gene_symbol":"AC023632.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94565036,"end":94565715,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166220.12","gene_symbol":"TBATA","gene_name":"thymus, brain and testes associated [Source:HGNC Symbol;Acc:HGNC:23511]","synonyms":"spatial,FLJ32820,C10orf27","biotype":"protein_coding","ncbi_id":"219793","summary":"This gene encodes a protein that regulates thymic epithelial cell proliferation and thymus size. It has been identified as a ligand for the class I human leukocyte antigen (HLA-I) in thymus. Studies of the orthologous mouse protein suggest that it may also play a role in spermatid differentiation, as well as in neuronal morphogenesis and synaptic plasticity. Polymorphisms in this gene are associated with susceptibility for multiple sclerosis (MS). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":70771239,"end":70785401,"strand":-1,"description":"thymus, brain and testes associated [Source:HGNC Symbol;Acc:HGNC:23511]"}, {"versioned_ensembl_gene_id":"ENSG00000224852.1","gene_symbol":"MTND5P24","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42286]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873262","summary":null,"start":143094789,"end":143096555,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42286]"}, {"versioned_ensembl_gene_id":"ENSG00000253704.1","gene_symbol":"AC023632.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":94553722,"end":94569745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282173.1","gene_symbol":"AC245427.5","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142788498,"end":142788547,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220541.4","gene_symbol":"AC233289.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113522482,"end":113522989,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280726.2","gene_symbol":"PCAT19","gene_name":"prostate cancer associated transcript 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49593]","synonyms":"LOC100505495,LINC01190","biotype":"lincRNA","ncbi_id":"100505495","summary":null,"start":41479081,"end":41500644,"strand":-1,"description":"prostate cancer associated transcript 19 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:49593]"}, {"versioned_ensembl_gene_id":"ENSG00000270524.1","gene_symbol":"QTRT1P1","gene_name":"queuine tRNA-ribosyltransferase catalytic subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39179]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420656","summary":null,"start":113882590,"end":113883667,"strand":1,"description":"queuine tRNA-ribosyltransferase catalytic subunit 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39179]"}, {"versioned_ensembl_gene_id":"ENSG00000213300.5","gene_symbol":"HNRNPA3P6","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48495]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653115","summary":null,"start":75214631,"end":75215636,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48495]"}, {"versioned_ensembl_gene_id":"ENSG00000241743.2","gene_symbol":"XACT","gene_name":"X active specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:45056]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105463123","summary":"This gene produces a spliced long non-coding RNA that is thought to play a role in the control of X-chromosome inactivation (XCI). This transcript has been shown to specifically coat the active X chromosome in human pluripotent cells. [provided by RefSeq, Mar 2015]","start":113616300,"end":113938218,"strand":-1,"description":"X active specific transcript (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:45056]"}, {"versioned_ensembl_gene_id":"ENSG00000271686.1","gene_symbol":"AL953862.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114389135,"end":114389954,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223680.10","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"CD167,NEP,PTK3A,CAK,EDDR1,NTRK4,RTK6","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30959531,"end":30970646,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000230502.1","gene_symbol":"AL953862.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114388988,"end":114389155,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232540.1","gene_symbol":"RPL36P19","gene_name":"ribosomal protein L36 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873855","summary":null,"start":43394525,"end":43394825,"strand":1,"description":"ribosomal protein L36 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42648]"}, {"versioned_ensembl_gene_id":"ENSG00000114999.7","gene_symbol":"TTL","gene_name":"tubulin tyrosine ligase [Source:HGNC Symbol;Acc:HGNC:21586]","synonyms":"MGC46235","biotype":"protein_coding","ncbi_id":"150465","summary":"TTL is a cytosolic enzyme involved in the posttranslational modification of alpha-tubulin (see MIM 602529). Alpha-tubulin within assembled microtubules is detyrosinated over time at the C terminus. After microtubule disassembly, TTL restores the tyrosine residues and consequently participates in a cycle of tubulin detyrosination and tyrosination (Erck et al., 2003 [PubMed 14571137]).[supplied by OMIM, Mar 2008]","start":112482154,"end":112541739,"strand":1,"description":"tubulin tyrosine ligase [Source:HGNC Symbol;Acc:HGNC:21586]"}, {"versioned_ensembl_gene_id":"ENSG00000233821.1","gene_symbol":"ENOX1-AS1","gene_name":"ENOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42396]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874129","summary":null,"start":43543918,"end":43548056,"strand":1,"description":"ENOX1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42396]"}, {"versioned_ensembl_gene_id":"ENSG00000100253.12","gene_symbol":"MIOX","gene_name":"myo-inositol oxygenase [Source:HGNC Symbol;Acc:HGNC:14522]","synonyms":"ALDRL6","biotype":"protein_coding","ncbi_id":"55586","summary":null,"start":50486784,"end":50490648,"strand":1,"description":"myo-inositol oxygenase [Source:HGNC Symbol;Acc:HGNC:14522]"}, {"versioned_ensembl_gene_id":"ENSG00000120658.13","gene_symbol":"ENOX1","gene_name":"ecto-NOX disulfide-thiol exchanger 1 [Source:HGNC Symbol;Acc:HGNC:25474]","synonyms":"cCNOX,PIG38,FLJ10094,CNOX","biotype":"protein_coding","ncbi_id":"55068","summary":"The protein encoded by this gene is involved in plasma membrane electron transport pathways. The encoded protein has both a hydroquinone (NADH) oxidase activity and a protein disulfide-thiol interchange activity. The two activities cycle with a periodicity of 24 minutes, with one activity being at its peak when the other is at its lowest. [provided by RefSeq, Dec 2016]","start":43213518,"end":43786908,"strand":-1,"description":"ecto-NOX disulfide-thiol exchanger 1 [Source:HGNC Symbol;Acc:HGNC:25474]"}, {"versioned_ensembl_gene_id":"ENSG00000231895.1","gene_symbol":"HLA-DPA3","gene_name":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"267013","summary":null,"start":33170244,"end":33170370,"strand":-1,"description":"major histocompatibility complex, class II, DP alpha 3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:19393]"}, {"versioned_ensembl_gene_id":"ENSG00000236961.1","gene_symbol":"AL136131.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43722786,"end":43737834,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235810.1","gene_symbol":"AL731534.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57513157,"end":57513425,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217281.4","gene_symbol":"LYPLA2P1","gene_name":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]","synonyms":"APT,LYPLA2L,dJ570F3.6","biotype":"processed_pseudogene","ncbi_id":"653639","summary":null,"start":33404609,"end":33405304,"strand":-1,"description":"lysophospholipase II pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21069]"}, {"versioned_ensembl_gene_id":"ENSG00000248496.3","gene_symbol":"ZBED9","gene_name":"zinc finger BED-type containing 9 [Source:HGNC Symbol;Acc:HGNC:13851]","synonyms":"ZNF452,ZNF305P2,ZFP38-L,SCAND3,KIAA1925,FLJ31087,Buster4","biotype":"protein_coding","ncbi_id":"114821","summary":null,"start":28573507,"end":28587330,"strand":-1,"description":"zinc finger BED-type containing 9 [Source:HGNC Symbol;Acc:HGNC:13851]"}, {"versioned_ensembl_gene_id":"ENSG00000257391.1","gene_symbol":"AC126763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":15154903,"end":15157020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281725.1","gene_symbol":"ELMO2P1","gene_name":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729894","summary":null,"start":23087871,"end":23126101,"strand":1,"description":"engulfment and cell motility 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38008]"}, {"versioned_ensembl_gene_id":"ENSG00000277770.1","gene_symbol":"AC137803.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":15358978,"end":15362674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183793.13","gene_symbol":"NPIPA5","gene_name":"nuclear pore complex interacting protein family member A5 [Source:HGNC Symbol;Acc:HGNC:41980]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288332","summary":null,"start":15363624,"end":15381047,"strand":-1,"description":"nuclear pore complex interacting protein family member A5 [Source:HGNC Symbol;Acc:HGNC:41980]"}, {"versioned_ensembl_gene_id":"ENSG00000186207.4","gene_symbol":"LCE5A","gene_name":"late cornified envelope 5A [Source:HGNC Symbol;Acc:HGNC:16614]","synonyms":"SPRL5A,LEP18","biotype":"protein_coding","ncbi_id":"254910","summary":null,"start":152510844,"end":152512177,"strand":1,"description":"late cornified envelope 5A [Source:HGNC Symbol;Acc:HGNC:16614]"}, {"versioned_ensembl_gene_id":"ENSG00000106003.12","gene_symbol":"LFNG","gene_name":"LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:6560]","synonyms":"SCDO3","biotype":"protein_coding","ncbi_id":"3955","summary":"This gene is a member of the glycosyltransferase 31 gene family. Members of this gene family, which also includes the MFNG (GeneID: 4242) and RFNG (GeneID: 5986) genes, encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, these proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling. The protein encoded by this gene is predicted to be a single-pass type II Golgi membrane protein but it may also be secreted and proteolytically processed like the related proteins in mouse and Drosophila (PMID: 9187150). Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. [provided by RefSeq, May 2018]","start":2512529,"end":2529177,"strand":1,"description":"LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:HGNC:6560]"}, {"versioned_ensembl_gene_id":"ENSG00000139154.14","gene_symbol":"AEBP2","gene_name":"AE binding protein 2 [Source:HGNC Symbol;Acc:HGNC:24051]","synonyms":"MGC17922","biotype":"protein_coding","ncbi_id":"121536","summary":null,"start":19404045,"end":19720801,"strand":1,"description":"AE binding protein 2 [Source:HGNC Symbol;Acc:HGNC:24051]"}, {"versioned_ensembl_gene_id":"ENSG00000282851.1","gene_symbol":"BISPR","gene_name":"BST2 interferon stimulated positive regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:51290]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105221694","summary":null,"start":17405694,"end":17418904,"strand":1,"description":"BST2 interferon stimulated positive regulator (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:51290]"}, {"versioned_ensembl_gene_id":"ENSG00000204580.13","gene_symbol":"DDR1","gene_name":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]","synonyms":"NEP,PTK3A,CAK,EDDR1,NTRK4,RTK6,CD167","biotype":"protein_coding","ncbi_id":"780","summary":"Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]","start":30876421,"end":30900156,"strand":1,"description":"discoidin domain receptor tyrosine kinase 1 [Source:HGNC Symbol;Acc:HGNC:2730]"}, {"versioned_ensembl_gene_id":"ENSG00000232333.1","gene_symbol":"RPS27AP2","gene_name":"ribosomal protein S27a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16572]","synonyms":"dJ531H16.4","biotype":"processed_pseudogene","ncbi_id":"140752","summary":null,"start":17516843,"end":17517307,"strand":1,"description":"ribosomal protein S27a pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16572]"}, {"versioned_ensembl_gene_id":"ENSG00000279708.1","gene_symbol":"AC133637.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":89358841,"end":89360377,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090659.17","gene_symbol":"CD209","gene_name":"CD209 molecule [Source:HGNC Symbol;Acc:HGNC:1641]","synonyms":"DC-SIGN1,DC-SIGN,CLEC4L,CDSIGN","biotype":"protein_coding","ncbi_id":"30835","summary":"This gene encodes a C-type lectin that functions in cell adhesion and pathogen recognition. This receptor recognizes a wide range of evolutionarily divergent pathogens with a large impact on public health, including leprosy and tuberculosis mycobacteria, the Ebola, hepatitis C, HIV-1 and Dengue viruses, and the SARS-CoV acute respiratory syndrome coronavirus. The protein is organized into four distinct domains: a C-terminal carbohydrate recognition domain, a flexible tandem-repeat neck domain, a transmembrane region and an N-terminal cytoplasmic domain involved in internalization. This gene is closely related in terms of both sequence and function to a neighboring gene, CLEC4M (Gene ID: 10332), also known as L-SIGN. The two genes differ in viral recognition and expression patterns, with this gene showing high expression on the surface of dendritic cells. Polymorphisms in the neck region are associated with protection from HIV-1 infection, while single nucleotide polymorphisms in the promoter of this gene are associated with differing resistance and susceptibility to and severity of infectious disease, including rs4804803, which is associated with SARS severity. [provided by RefSeq, May 2020]","start":7739994,"end":7747564,"strand":-1,"description":"CD209 molecule [Source:HGNC Symbol;Acc:HGNC:1641]"}, {"versioned_ensembl_gene_id":"ENSG00000124795.14","gene_symbol":"DEK","gene_name":"DEK proto-oncogene [Source:HGNC Symbol;Acc:HGNC:2768]","synonyms":"D6S231E","biotype":"protein_coding","ncbi_id":"7913","summary":"This gene encodes a protein with one SAP domain. This protein binds to cruciform and superhelical DNA and induces positive supercoils into closed circular DNA, and is also involved in splice site selection during mRNA processing. Chromosomal aberrations involving this region, increased expression of this gene, and the presence of antibodies against this protein are all associated with various diseases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]","start":18223868,"end":18264823,"strand":-1,"description":"DEK proto-oncogene [Source:HGNC Symbol;Acc:HGNC:2768]"}, {"versioned_ensembl_gene_id":"ENSG00000228868.3","gene_symbol":"MYLKP1","gene_name":"myosin light chain kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7591]","synonyms":"MYLKP","biotype":"unprocessed_pseudogene","ncbi_id":"9430","summary":null,"start":75328549,"end":75339071,"strand":-1,"description":"myosin light chain kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7591]"}, {"versioned_ensembl_gene_id":"ENSG00000259891.1","gene_symbol":"AC107375.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140505813,"end":140508043,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000126749.14","gene_symbol":"EMG1","gene_name":"EMG1, N1-specific pseudouridine methyltransferase [Source:HGNC Symbol;Acc:HGNC:16912]","synonyms":"Grcc2f,C2F,NEP1,Grcc2f,C2F,NEP1","biotype":"protein_coding","ncbi_id":"10436","summary":"This gene encodes an essential, conserved eukaryotic protein that methylates pseudouridine in 18S rRNA. The related protein in yeast is a component of the small subunit processome and is essential for biogenesis of the ribosomal 40S subunit. A mutation in this gene has been associated with Bowen-Conradi syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":6970893,"end":6979941,"strand":1,"description":"EMG1, N1-specific pseudouridine methyltransferase [Source:HGNC Symbol;Acc:HGNC:16912]"}, {"versioned_ensembl_gene_id":"ENSG00000243674.1","gene_symbol":"AC131233.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75347833,"end":75348787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223841.1","gene_symbol":"AC006484.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":57955295,"end":57957178,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179799.9","gene_symbol":"OR7E22P","gene_name":"olfactory receptor family 7 subfamily E member 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:8394]","synonyms":"OR6DG,OR3.6","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"9431","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":75356437,"end":75362268,"strand":-1,"description":"olfactory receptor family 7 subfamily E member 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:8394]"}, {"versioned_ensembl_gene_id":"ENSG00000241250.1","gene_symbol":"AC022483.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56710060,"end":56710614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278869.1","gene_symbol":"BX539320.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49933198,"end":49934074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238189.2","gene_symbol":"ENOX1-AS2","gene_name":"ENOX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42397]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874130","summary":null,"start":43458465,"end":43459484,"strand":1,"description":"ENOX1 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42397]"}, {"versioned_ensembl_gene_id":"ENSG00000176383.8","gene_symbol":"B3GNT4","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:15683]","synonyms":"beta3Gn-T4,B3GN-T4","biotype":"protein_coding","ncbi_id":"79369","summary":"This gene encodes a member of the beta-1,3-N-acetylglucosaminyltransferase protein family. The encoded enzyme is involved in the biosynthesis of poly-N-acetyllactosamine chains and prefers lacto-N-neotetraose as a substrate. It is a type II transmembrane protein. [provided by RefSeq, Jul 2008]","start":122203543,"end":122208952,"strand":1,"description":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4 [Source:HGNC Symbol;Acc:HGNC:15683]"}, {"versioned_ensembl_gene_id":"ENSG00000198178.10","gene_symbol":"CLEC4C","gene_name":"C-type lectin domain family 4 member C [Source:HGNC Symbol;Acc:HGNC:13258]","synonyms":"HECL,DLEC,CLECSF7,CLECSF11,CD303,BDCA2","biotype":"protein_coding","ncbi_id":"170482","summary":"This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may play a role in dendritic cell function. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":7729415,"end":7751605,"strand":-1,"description":"C-type lectin domain family 4 member C [Source:HGNC Symbol;Acc:HGNC:13258]"}, {"versioned_ensembl_gene_id":"ENSG00000226883.1","gene_symbol":"AL035416.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":59754747,"end":59789182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197616.11","gene_symbol":"MYH6","gene_name":"myosin heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:7576]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4624","summary":"Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located approximately 4kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3. [provided by RefSeq, Feb 2017]","start":23381990,"end":23408277,"strand":-1,"description":"myosin heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:7576]"}, {"versioned_ensembl_gene_id":"ENSG00000123136.14","gene_symbol":"DDX39A","gene_name":"DExD-box helicase 39A [Source:HGNC Symbol;Acc:HGNC:17821]","synonyms":"URH49,DDXL,DDX39,BAT1L","biotype":"protein_coding","ncbi_id":"10212","summary":"This gene encodes a member of the DEAD box protein family. These proteins are characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD) and are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene is thought to play a role in the prognosis of patients with gastrointestinal stromal tumors. A pseudogene of this gene is present on chromosome 13. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Sep 2013]","start":14408819,"end":14419383,"strand":-1,"description":"DExD-box helicase 39A [Source:HGNC Symbol;Acc:HGNC:17821]"}, {"versioned_ensembl_gene_id":"ENSG00000172456.17","gene_symbol":"FGGY","gene_name":"FGGY carbohydrate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:25610]","synonyms":"FLJ10986","biotype":"protein_coding","ncbi_id":"55277","summary":"This gene encodes a protein that phosphorylates carbohydrates such as ribulose, ribitol, and L-arabinitol. Genome-wide association studies in some populations have found an association between polymorphisms in this gene and sporadic amyotrophic lateral sclerosis, but studies of other populations have not been able to replicate this association. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":59296638,"end":59810647,"strand":1,"description":"FGGY carbohydrate kinase domain containing [Source:HGNC Symbol;Acc:HGNC:25610]"}, {"versioned_ensembl_gene_id":"ENSG00000135451.12","gene_symbol":"TROAP","gene_name":"trophinin associated protein [Source:HGNC Symbol;Acc:HGNC:12327]","synonyms":"TASTIN","biotype":"protein_coding","ncbi_id":"10024","summary":null,"start":49323236,"end":49331731,"strand":1,"description":"trophinin associated protein [Source:HGNC Symbol;Acc:HGNC:12327]"}, {"versioned_ensembl_gene_id":"ENSG00000146731.10","gene_symbol":"CCT6A","gene_name":"chaperonin containing TCP1 subunit 6A [Source:HGNC Symbol;Acc:HGNC:1620]","synonyms":"TCPZ,TCP20,HTR3,Cctz,CCT6,TTCP20","biotype":"protein_coding","ncbi_id":"908","summary":"The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternate transcriptional splice variants of this gene, encoding different isoforms, have been characterized. In addition, several pseudogenes of this gene have been located. [provided by RefSeq, Jun 2010]","start":56051630,"end":56063989,"strand":1,"description":"chaperonin containing TCP1 subunit 6A [Source:HGNC Symbol;Acc:HGNC:1620]"}, {"versioned_ensembl_gene_id":"ENSG00000229873.1","gene_symbol":"OGFR-AS1","gene_name":"OGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40724]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101409261","summary":null,"start":62800627,"end":62805587,"strand":-1,"description":"OGFR antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40724]"}, {"versioned_ensembl_gene_id":"ENSG00000218107.1","gene_symbol":"AL136131.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":43705949,"end":43706751,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139719.9","gene_symbol":"VPS33A","gene_name":"VPS33A, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:18179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"65082","summary":"This gene encodes a tethering protein and a core subunit of the homotypic fusion and protein sorting (HOPS) complex. The HOPS complex and a second endosomal tethering complex called the class C core vacuole/endosome tethering (CORVET) complex, perform diverse functions in endocytosis including membrane tethering, RabGTPase interaction, activation and proofreading of synaptic-soluble N-ethylmaleimide-sensitive factor attachment receptor (SNARE) assembly to drive membrane fusion, and endosome-to-cytoskeleton attachment. The HOPS complex controls endosome maturation as well as endosome traffic to the lysosome. This complex is essential for vacuolar fusion and is required for adaptor protein complex 3-dependent transport from the golgi to the vacuole. The encoded protein belongs to the Sec1/Munc18 (SM) family of SNARE-mediated membrane fusion regulators. Naturally occurring mutations in this gene are associated with a novel mucopolysaccharidosis-like disease. [provided by RefSeq, Apr 2017]","start":122229564,"end":122266521,"strand":-1,"description":"VPS33A, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:18179]"}, {"versioned_ensembl_gene_id":"ENSG00000182718.16","gene_symbol":"ANXA2","gene_name":"annexin A2 [Source:HGNC Symbol;Acc:HGNC:537]","synonyms":"LPC2D,LIP2,CAL1H,ANX2L4,ANX2","biotype":"protein_coding","ncbi_id":"302","summary":"This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. This protein functions as an autocrine factor which heightens osteoclast formation and bone resorption. This gene has three pseudogenes located on chromosomes 4, 9 and 10, respectively. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. Annexin A2 expression has been found to correlate with resistance to treatment against various cancer forms. [provided by RefSeq, Dec 2019]","start":60347134,"end":60402883,"strand":-1,"description":"annexin A2 [Source:HGNC Symbol;Acc:HGNC:537]"}, {"versioned_ensembl_gene_id":"ENSG00000257078.1","gene_symbol":"AC006512.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7041156,"end":7041641,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215021.8","gene_symbol":"PHB2","gene_name":"prohibitin 2 [Source:HGNC Symbol;Acc:HGNC:30306]","synonyms":"REA,p22,BCAP37,Bap37","biotype":"protein_coding","ncbi_id":"11331","summary":null,"start":6965327,"end":6970825,"strand":-1,"description":"prohibitin 2 [Source:HGNC Symbol;Acc:HGNC:30306]"}, {"versioned_ensembl_gene_id":"ENSG00000258168.5","gene_symbol":"AC025569.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70468080,"end":70543040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234197.1","gene_symbol":"ETV5-AS1","gene_name":"ETV5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40222]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873934","summary":null,"start":186079170,"end":186080947,"strand":1,"description":"ETV5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40222]"}, {"versioned_ensembl_gene_id":"ENSG00000230042.1","gene_symbol":"AK3P3","gene_name":"adenylate kinase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39062]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419075","summary":null,"start":23129178,"end":23129841,"strand":1,"description":"adenylate kinase 3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39062]"}, {"versioned_ensembl_gene_id":"ENSG00000244405.7","gene_symbol":"ETV5","gene_name":"ETS variant 5 [Source:HGNC Symbol;Acc:HGNC:3494]","synonyms":"ERM","biotype":"protein_coding","ncbi_id":"2119","summary":null,"start":186046308,"end":186110318,"strand":-1,"description":"ETS variant 5 [Source:HGNC Symbol;Acc:HGNC:3494]"}, {"versioned_ensembl_gene_id":"ENSG00000122550.17","gene_symbol":"KLHL7","gene_name":"kelch like family member 7 [Source:HGNC Symbol;Acc:HGNC:15646]","synonyms":"SBBI26,RP42,KLHL6","biotype":"protein_coding","ncbi_id":"55975","summary":"This gene encodes a BTB-Kelch-related protein. The encoded protein may be involved in protein degradation. Mutations in this gene have been associated with retinitis pigmentosa 42. [provided by RefSeq, Feb 2010]","start":23105758,"end":23177914,"strand":1,"description":"kelch like family member 7 [Source:HGNC Symbol;Acc:HGNC:15646]"}, {"versioned_ensembl_gene_id":"ENSG00000213107.2","gene_symbol":"AHCYP5","gene_name":"adenosylhomocysteinase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44997]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391470","summary":null,"start":195582794,"end":195584031,"strand":-1,"description":"adenosylhomocysteinase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44997]"}, {"versioned_ensembl_gene_id":"ENSG00000275675.1","gene_symbol":"AL161931.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38068449,"end":38068694,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269481.1","gene_symbol":"AC010319.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17414257,"end":17422324,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226086.5","gene_symbol":"EIF3LP3","gene_name":"eukaryotic translation initiation factor 3 subunit L pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44976]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"340947","summary":null,"start":38080056,"end":38080877,"strand":-1,"description":"eukaryotic translation initiation factor 3 subunit L pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44976]"}, {"versioned_ensembl_gene_id":"ENSG00000235964.1","gene_symbol":"FXYD6P2","gene_name":"FXYD domain containing ion transport regulator 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4032]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128512","summary":null,"start":38091764,"end":38092051,"strand":-1,"description":"FXYD domain containing ion transport regulator 6 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:4032]"}, {"versioned_ensembl_gene_id":"ENSG00000143624.13","gene_symbol":"INTS3","gene_name":"integrator complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26153]","synonyms":"SOSS-A,INT3,FLJ21919,C1orf60","biotype":"protein_coding","ncbi_id":"65123","summary":"The protein encoded by this gene can form a complex with human single-strand DNA binding proteins 1 or 2 (hSSB1 and hSSB2) and other proteins to mediate genome stability and the DNA damage response. The encoded protein is also part of a multiprotein complex that interacts with the C-terminal domain of RNA polymerase II large subunit to help regulate processing of U1 and U2 small nuclear RNAs. [provided by RefSeq, May 2016]","start":153728067,"end":153774808,"strand":1,"description":"integrator complex subunit 3 [Source:HGNC Symbol;Acc:HGNC:26153]"}, {"versioned_ensembl_gene_id":"ENSG00000109424.3","gene_symbol":"UCP1","gene_name":"uncoupling protein 1 [Source:HGNC Symbol;Acc:HGNC:12517]","synonyms":"UCP,SLC25A7","biotype":"protein_coding","ncbi_id":"7350","summary":"Mitochondrial uncoupling proteins (UCP) are members of the family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. This gene is expressed only in brown adipose tissue, a specialized tissue which functions to produce heat. [provided by RefSeq, Jul 2008]","start":140559434,"end":140568805,"strand":-1,"description":"uncoupling protein 1 [Source:HGNC Symbol;Acc:HGNC:12517]"}, {"versioned_ensembl_gene_id":"ENSG00000164188.8","gene_symbol":"RANBP3L","gene_name":"RAN binding protein 3 like [Source:HGNC Symbol;Acc:HGNC:26353]","synonyms":"FLJ25422","biotype":"protein_coding","ncbi_id":"202151","summary":null,"start":36248434,"end":36302114,"strand":-1,"description":"RAN binding protein 3 like [Source:HGNC Symbol;Acc:HGNC:26353]"}, {"versioned_ensembl_gene_id":"ENSG00000127329.15","gene_symbol":"PTPRB","gene_name":"protein tyrosine phosphatase, receptor type B [Source:HGNC Symbol;Acc:HGNC:9665]","synonyms":"PTPB","biotype":"protein_coding","ncbi_id":"5787","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and one intracytoplasmic catalytic domain, thus belongs to receptor type PTP. The extracellular region of this PTP is composed of multiple fibronectin type_III repeats, which was shown to interact with neuronal receptor and cell adhesion molecules, such as contactin and tenascin C. This protein was also found to interact with sodium channels, and thus may regulate sodium channels by altering tyrosine phosphorylation status. The functions of the interaction partners of this protein implicate the roles of this PTP in cell adhesion, neurite growth, and neuronal differentiation. Alternate transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]","start":70515866,"end":70637440,"strand":-1,"description":"protein tyrosine phosphatase, receptor type B [Source:HGNC Symbol;Acc:HGNC:9665]"}, {"versioned_ensembl_gene_id":"ENSG00000261197.2","gene_symbol":"AC133561.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34051140,"end":34051363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262561.1","gene_symbol":"AC136932.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":34120470,"end":34120677,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143363.15","gene_symbol":"PRUNE1","gene_name":"prune exopolyphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:13420]","synonyms":"PRUNE,HTCD37,H-PRUNE,DRES-17","biotype":"protein_coding","ncbi_id":"58497","summary":"This gene encodes a member of the DHH protein superfamily of phosphoesterases. This protein has been found to function as both a nucleotide phosphodiesterase and an exopolyphosphatase. This protein is believed to stimulate cancer progression and metastases through the induction of cell motility. A pseuodgene has been identified on chromosome 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":151008420,"end":151035713,"strand":1,"description":"prune exopolyphosphatase 1 [Source:HGNC Symbol;Acc:HGNC:13420]"}, {"versioned_ensembl_gene_id":"ENSG00000271231.1","gene_symbol":"KRT18P9","gene_name":"keratin 18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17767]","synonyms":"bA513I15.2","biotype":"processed_pseudogene","ncbi_id":"442205","summary":null,"start":34189780,"end":34191079,"strand":1,"description":"keratin 18 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:17767]"}, {"versioned_ensembl_gene_id":"ENSG00000248621.2","gene_symbol":"AC108019.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":140600401,"end":140600575,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214810.4","gene_symbol":"CYCSP55","gene_name":"cytochrome c, somatic pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:21252]","synonyms":"HCP15,CYCSL1,bA513I15.3","biotype":"processed_pseudogene","ncbi_id":"157317","summary":null,"start":34219439,"end":34220066,"strand":1,"description":"cytochrome c, somatic pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:21252]"}, {"versioned_ensembl_gene_id":"ENSG00000196850.5","gene_symbol":"PPTC7","gene_name":"PTC7 protein phosphatase homolog [Source:HGNC Symbol;Acc:HGNC:30695]","synonyms":"TA-PP2C","biotype":"protein_coding","ncbi_id":"160760","summary":null,"start":110533245,"end":110583320,"strand":-1,"description":"PTC7 protein phosphatase homolog [Source:HGNC Symbol;Acc:HGNC:30695]"}, {"versioned_ensembl_gene_id":"ENSG00000185668.7","gene_symbol":"POU3F1","gene_name":"POU class 3 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9214]","synonyms":"SCIP,OTF6,OCT6","biotype":"protein_coding","ncbi_id":"5453","summary":null,"start":38044611,"end":38046794,"strand":-1,"description":"POU class 3 homeobox 1 [Source:HGNC Symbol;Acc:HGNC:9214]"}, {"versioned_ensembl_gene_id":"ENSG00000226547.2","gene_symbol":"SSU72P1","gene_name":"SSU72 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43620]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286528","summary":null,"start":114390674,"end":114391256,"strand":1,"description":"SSU72 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43620]"}, {"versioned_ensembl_gene_id":"ENSG00000224592.5","gene_symbol":"AL139158.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38047314,"end":38119025,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000100379.17","gene_symbol":"KCTD17","gene_name":"potassium channel tetramerization domain containing 17 [Source:HGNC Symbol;Acc:HGNC:25705]","synonyms":"FLJ12242","biotype":"protein_coding","ncbi_id":"79734","summary":"This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26. [provided by RefSeq, Nov 2016]","start":37051736,"end":37063390,"strand":1,"description":"potassium channel tetramerization domain containing 17 [Source:HGNC Symbol;Acc:HGNC:25705]"}, {"versioned_ensembl_gene_id":"ENSG00000233115.4","gene_symbol":"FAM90A11P","gene_name":"family with sequence similarity 90 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:32259]","synonyms":"FAM90A11","biotype":"unprocessed_pseudogene","ncbi_id":"441331","summary":null,"start":8011782,"end":8017011,"strand":-1,"description":"family with sequence similarity 90 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:32259]"}, {"versioned_ensembl_gene_id":"ENSG00000267304.1","gene_symbol":"AC004637.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":3672582,"end":3674295,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223589.2","gene_symbol":"AL139158.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38080572,"end":38080911,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186111.9","gene_symbol":"PIP5K1C","gene_name":"phosphatidylinositol-4-phosphate 5-kinase type 1 gamma [Source:HGNC Symbol;Acc:HGNC:8996]","synonyms":"PIP5Kgamma,LCCS3,KIAA0589","biotype":"protein_coding","ncbi_id":"23396","summary":"This locus encodes a type I phosphatidylinositol 4-phosphate 5-kinase. The encoded protein catalyzes phosphorylation of phosphatidylinositol 4-phosphate, producing phosphatidylinositol 4,5-bisphosphate. This enzyme is found at synapses and has been found to play roles in endocytosis and cell migration. Mutations at this locus have been associated with lethal congenital contractural syndrome. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Sep 2010]","start":3630183,"end":3700479,"strand":-1,"description":"phosphatidylinositol-4-phosphate 5-kinase type 1 gamma [Source:HGNC Symbol;Acc:HGNC:8996]"}, {"versioned_ensembl_gene_id":"ENSG00000231821.1","gene_symbol":"NPM1P48","gene_name":"nucleophosmin 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:45227]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442006","summary":null,"start":4514204,"end":4515056,"strand":-1,"description":"nucleophosmin 1 pseudogene 48 [Source:HGNC Symbol;Acc:HGNC:45227]"}, {"versioned_ensembl_gene_id":"ENSG00000147246.9","gene_symbol":"HTR2C","gene_name":"5-hydroxytryptamine receptor 2C [Source:HGNC Symbol;Acc:HGNC:5295]","synonyms":"HTR1C,5HTR2C,5-HT2C","biotype":"protein_coding","ncbi_id":"3358","summary":"This gene encodes a seven-transmembrane G-protein-coupled receptor. The encoded protein responds to signaling through the neurotransmitter serotonin. The mRNA of this gene is subject to multiple RNA editing events, where adenosine residues encoded by the genome are converted to inosines. RNA editing is predicted to alter the structure of the second intracellular loop, thereby generating alternate protein forms with decreased ability to interact with G proteins. Abnormalities in RNA editing of this gene have been detected in victims of suicide that suffer from depression. In addition, naturally-occuring variation in the promoter and 5' non-coding and coding regions of this gene may show statistically-significant association with mental illness and behavioral disorders. Alternative splicing results in multiple different transcript variants. [provided by RefSeq, Jan 2015]","start":114584078,"end":114910061,"strand":1,"description":"5-hydroxytryptamine receptor 2C [Source:HGNC Symbol;Acc:HGNC:5295]"}, {"versioned_ensembl_gene_id":"ENSG00000275918.4","gene_symbol":"KIR3DX1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]","synonyms":"FLJ00060,LENG12","biotype":"protein_coding","ncbi_id":"90011","summary":null,"start":54540656,"end":54553413,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains X1 [Source:HGNC Symbol;Acc:HGNC:25043]"}, {"versioned_ensembl_gene_id":"ENSG00000174206.12","gene_symbol":"C12orf66","gene_name":"chromosome 12 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:26517]","synonyms":"FLJ32549","biotype":"protein_coding","ncbi_id":"144577","summary":null,"start":64186316,"end":64222296,"strand":-1,"description":"chromosome 12 open reading frame 66 [Source:HGNC Symbol;Acc:HGNC:26517]"}, {"versioned_ensembl_gene_id":"ENSG00000256861.1","gene_symbol":"AC048338.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":122207779,"end":122266423,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204922.4","gene_symbol":"UQCC3","gene_name":"ubiquinol-cytochrome c reductase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:34399]","synonyms":"UNQ655,C11orf83","biotype":"protein_coding","ncbi_id":"790955","summary":"Complex III is a mitochondrial inner membrane protein complex that transfers electrons from ubiquinol to cytochrome c. This gene encodes a protein that functions in complex III assembly. Mutations in this gene result in Mitochondrial complex III deficiency, nuclear type 9. [provided by RefSeq, Dec 2014]","start":62670273,"end":62673687,"strand":1,"description":"ubiquinol-cytochrome c reductase complex assembly factor 3 [Source:HGNC Symbol;Acc:HGNC:34399]"}, {"versioned_ensembl_gene_id":"ENSG00000226113.1","gene_symbol":"AL133217.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38247922,"end":38333155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283930.1","gene_symbol":"AL117339.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38094368,"end":38360098,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234941.1","gene_symbol":"AL117339.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38250442,"end":38250603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075407.18","gene_symbol":"ZNF37A","gene_name":"zinc finger protein 37A [Source:HGNC Symbol;Acc:HGNC:13102]","synonyms":"ZNF37,KOX21","biotype":"protein_coding","ncbi_id":"7587","summary":null,"start":38094334,"end":38150293,"strand":1,"description":"zinc finger protein 37A [Source:HGNC Symbol;Acc:HGNC:13102]"}, {"versioned_ensembl_gene_id":"ENSG00000184047.16","gene_symbol":"DIABLO","gene_name":"diablo IAP-binding mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:21528]","synonyms":"SMAC,FLJ25049,FLJ10537,DIABLO-S,DFNA64","biotype":"protein_coding","ncbi_id":"56616","summary":"This gene encodes an inhibitor of apoptosis protein (IAP)-binding protein. The encoded mitochondrial protein enters the cytosol when cells undergo apoptosis, and allows activation of caspases by binding to inhibitor of apoptosis proteins. Overexpression of the encoded protein sensitizes tumor cells to apoptosis. A mutation in this gene is associated with young-adult onset of nonsyndromic deafness-64. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":122207662,"end":122227534,"strand":-1,"description":"diablo IAP-binding mitochondrial protein [Source:HGNC Symbol;Acc:HGNC:21528]"}, {"versioned_ensembl_gene_id":"ENSG00000162194.12","gene_symbol":"LBHD1","gene_name":"LBH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28351]","synonyms":"MGC2477,C11orf48","biotype":"protein_coding","ncbi_id":"79081","summary":"This gene shares three exons in common with another gene, chromosome 11 open reading frame 98 (GeneID:102288414), but the encoded protein uses a reading frame that is different from that of the chromosome 11 open reading frame 98 gene. [provided by RefSeq, Nov 2017]","start":62662817,"end":62672255,"strand":-1,"description":"LBH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28351]"}, {"versioned_ensembl_gene_id":"ENSG00000228105.1","gene_symbol":"LINC01757","gene_name":"long intergenic non-protein coding RNA 1757 [Source:HGNC Symbol;Acc:HGNC:52546]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376827","summary":null,"start":20243095,"end":20244655,"strand":1,"description":"long intergenic non-protein coding RNA 1757 [Source:HGNC Symbol;Acc:HGNC:52546]"}, {"versioned_ensembl_gene_id":"ENSG00000284710.1","gene_symbol":"Z98257.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20272018,"end":20275005,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235668.1","gene_symbol":"CR936879.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28837874,"end":28839011,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231114.1","gene_symbol":"AC078842.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":137318592,"end":137326953,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068394.10","gene_symbol":"GPKOW","gene_name":"G-patch domain and KOW motifs [Source:HGNC Symbol;Acc:HGNC:30677]","synonyms":"Spp2,GPATCH5,GPATC5,T54","biotype":"protein_coding","ncbi_id":"27238","summary":"This gene encodes a putative RNA-binding protein containing G-patch and KOW (Kyprides, Ouzounis, Woese) domains. The encoded protein interacts directly with protein kinase A and protein kinase X and is also found associated with the spliceosome. [provided by RefSeq, Aug 2013]","start":49113389,"end":49123801,"strand":-1,"description":"G-patch domain and KOW motifs [Source:HGNC Symbol;Acc:HGNC:30677]"}, {"versioned_ensembl_gene_id":"ENSG00000105894.11","gene_symbol":"PTN","gene_name":"pleiotrophin [Source:HGNC Symbol;Acc:HGNC:9630]","synonyms":"NEGF1,HBNF,HBGF8","biotype":"protein_coding","ncbi_id":"5764","summary":"The protein encoded by this gene is a secreted heparin-binding growth factor. The protein has significant roles in cell growth and survival, cell migration, angiogenesis and tumorigenesis. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016]","start":137227341,"end":137343865,"strand":-1,"description":"pleiotrophin [Source:HGNC Symbol;Acc:HGNC:9630]"}, {"versioned_ensembl_gene_id":"ENSG00000099219.13","gene_symbol":"ERMP1","gene_name":"endoplasmic reticulum metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:23703]","synonyms":"KIAA1815,FXNA,FLJ23309","biotype":"protein_coding","ncbi_id":"79956","summary":null,"start":5765076,"end":5833117,"strand":-1,"description":"endoplasmic reticulum metallopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:23703]"}, {"versioned_ensembl_gene_id":"ENSG00000058866.14","gene_symbol":"DGKG","gene_name":"diacylglycerol kinase gamma [Source:HGNC Symbol;Acc:HGNC:2853]","synonyms":"DAGK3","biotype":"protein_coding","ncbi_id":"1608","summary":"This gene encodes an enzyme that is a member of the type I subfamily of diacylglycerol kinases, which are involved in lipid metabolism. These enzymes generate phosphatidic acid by catalyzing the phosphorylation of diacylglycerol, a fundamental lipid second messenger that activates numerous proteins, including protein kinase C isoforms, Ras guanyl nucleotide-releasing proteins and some transient receptor potential channels. Diacylglycerol kinase gamma has been implicated in cell cycle regulation and in the negative regulation of macrophage differentiation in leukemia cells. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":186105668,"end":186362237,"strand":-1,"description":"diacylglycerol kinase gamma [Source:HGNC Symbol;Acc:HGNC:2853]"}, {"versioned_ensembl_gene_id":"ENSG00000224664.2","gene_symbol":"RPL36AP53","gene_name":"ribosomal protein L36a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36517]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271611","summary":null,"start":114589620,"end":114589935,"strand":1,"description":"ribosomal protein L36a pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:36517]"}, {"versioned_ensembl_gene_id":"ENSG00000234904.1","gene_symbol":"CR936879.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28861420,"end":28862051,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270413.1","gene_symbol":"AL355812.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":114900359,"end":114900574,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234966.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28859629,"end":28863351,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000224773.2","gene_symbol":"HSPA8P7","gene_name":"heat shock protein family A (Hsp70) member 8 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:44922]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420080","summary":null,"start":114774828,"end":114776775,"strand":-1,"description":"heat shock protein family A (Hsp70) 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{"versioned_ensembl_gene_id":"ENSG00000258181.1","gene_symbol":"AC008083.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47248124,"end":47257539,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257925.1","gene_symbol":"AC008083.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47237734,"end":47279021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224761.4","gene_symbol":"AL117339.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38164648,"end":38212417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276454.1","gene_symbol":"AC008083.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47265665,"end":47266108,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284623.1","gene_symbol":"AL139158.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38129464,"end":38140593,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282780.1","gene_symbol":"AC245427.9","gene_name":null,"synonyms":null,"biotype":"TR_J_gene","ncbi_id":null,"summary":null,"start":142788988,"end":142789040,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279635.1","gene_symbol":"AC091895.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8980404,"end":8980659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237290.1","gene_symbol":"LINC01343","gene_name":"long intergenic non-protein coding RNA 1343 [Source:HGNC Symbol;Acc:HGNC:50553]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339442","summary":null,"start":38209034,"end":38214767,"strand":-1,"description":"long intergenic non-protein 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{"versioned_ensembl_gene_id":"ENSG00000112902.11","gene_symbol":"SEMA5A","gene_name":"semaphorin 5A [Source:HGNC Symbol;Acc:HGNC:10736]","synonyms":"semF,SEMAF","biotype":"protein_coding","ncbi_id":"9037","summary":"This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. 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[provided by RefSeq, Aug 2011]","start":10944488,"end":11182189,"strand":1,"description":"C-type lectin domain containing 16A [Source:HGNC Symbol;Acc:HGNC:29013]"}, {"versioned_ensembl_gene_id":"ENSG00000215237.6","gene_symbol":"AL592293.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":14993312,"end":15019729,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257906.1","gene_symbol":"LINC02156","gene_name":"long intergenic non-protein coding RNA 2156 [Source:HGNC Symbol;Acc:HGNC:53017]","synonyms":"RP1-90J4.1","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":47415008,"end":47420179,"strand":1,"description":"long intergenic non-protein coding RNA 2156 [Source:HGNC Symbol;Acc:HGNC:53017]"}, {"versioned_ensembl_gene_id":"ENSG00000185085.2","gene_symbol":"INTS5","gene_name":"integrator complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29352]","synonyms":"KIAA1698,INT5","biotype":"protein_coding","ncbi_id":"80789","summary":"The Integrator complex is a complex that associates with the C-terminal domain of RNA polymerase II large subunit. This complex is brought to U1 and U2 small nuclear RNA genes, where it is involved in the transcription and processing of their transcripts. The protein encoded by this gene represents a subunit of the Integrator complex. [provided by RefSeq, Aug 2016]","start":62646848,"end":62653302,"strand":-1,"description":"integrator complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:29352]"}, {"versioned_ensembl_gene_id":"ENSG00000228585.1","gene_symbol":"AC073143.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":5313740,"end":5314134,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234297.2","gene_symbol":"AL592293.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":15055057,"end":15056052,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254229.2","gene_symbol":"FAM90A12P","gene_name":"family with sequence similarity 90 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:32260]","synonyms":"FAM90A12","biotype":"unprocessed_pseudogene","ncbi_id":"645879","summary":"FAM90A12 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Jul 2010]","start":8027077,"end":8032305,"strand":-1,"description":"family with sequence similarity 90 member A12, pseudogene [Source:HGNC Symbol;Acc:HGNC:32260]"}, {"versioned_ensembl_gene_id":"ENSG00000271969.1","gene_symbol":"U47924.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":6964949,"end":6965382,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232000.2","gene_symbol":"CLCN3P1","gene_name":"chloride voltage-gated channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49775]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100419056","summary":null,"start":14987302,"end":15146401,"strand":-1,"description":"chloride voltage-gated channel 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49775]"}, {"versioned_ensembl_gene_id":"ENSG00000182326.14","gene_symbol":"C1S","gene_name":"complement C1s [Source:HGNC Symbol;Acc:HGNC:1247]","synonyms":null,"biotype":"protein_coding","ncbi_id":"716","summary":"This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency. [provided by RefSeq, Mar 2009]","start":6988259,"end":7071032,"strand":1,"description":"complement C1s [Source:HGNC Symbol;Acc:HGNC:1247]"}, {"versioned_ensembl_gene_id":"ENSG00000226664.1","gene_symbol":"AL020998.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20294211,"end":20323187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271462.1","gene_symbol":"AC091805.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19418927,"end":19419161,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158816.15","gene_symbol":"VWA5B1","gene_name":"von Willebrand factor A domain containing 5B1 [Source:HGNC Symbol;Acc:HGNC:26538]","synonyms":"FLJ32784","biotype":"protein_coding","ncbi_id":"127731","summary":null,"start":20290919,"end":20354894,"strand":1,"description":"von Willebrand factor A domain containing 5B1 [Source:HGNC Symbol;Acc:HGNC:26538]"}, {"versioned_ensembl_gene_id":"ENSG00000278247.2","gene_symbol":"GOLGA6L1","gene_name":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283767","summary":null,"start":23133045,"end":23141599,"strand":-1,"description":"golgin A6 family-like 1 [Source:HGNC Symbol;Acc:HGNC:37444]"}, {"versioned_ensembl_gene_id":"ENSG00000255909.1","gene_symbol":"PDCD5P1","gene_name":"programmed cell death 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49885]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100527946","summary":null,"start":19413153,"end":19413461,"strand":1,"description":"programmed cell death 5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49885]"}, {"versioned_ensembl_gene_id":"ENSG00000245205.3","gene_symbol":"EEF1A1P4","gene_name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3199]","synonyms":"EEF1AL2","biotype":"processed_pseudogene","ncbi_id":"100421854","summary":null,"start":19456244,"end":19457648,"strand":-1,"description":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:3199]"}, {"versioned_ensembl_gene_id":"ENSG00000240328.1","gene_symbol":"AC091805.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19508904,"end":19509245,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275478.1","gene_symbol":"AL671879.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28587373,"end":28591739,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278615.4","gene_symbol":"C11orf98","gene_name":"chromosome 11 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:51238]","synonyms":"C11orf48","biotype":"protein_coding","ncbi_id":"102288414","summary":"This gene shares three exons in common with another gene, LBH domain containing 1 (GeneID:79081), but the encoded protein uses a reading frame that is different from that of the LBH domain containing 1 gene. [provided by RefSeq, Nov 2017]","start":62662816,"end":62665217,"strand":-1,"description":"chromosome 11 open reading frame 98 [Source:HGNC Symbol;Acc:HGNC:51238]"}, {"versioned_ensembl_gene_id":"ENSG00000249032.1","gene_symbol":"LINC00533","gene_name":"long intergenic non-protein coding RNA 533 [Source:HGNC Symbol;Acc:HGNC:18690]","synonyms":"C6orf39,C6orf38,bA373N24.1","biotype":"processed_transcript","ncbi_id":"387055","summary":null,"start":28648243,"end":28654475,"strand":-1,"description":"long intergenic non-protein coding RNA 533 [Source:HGNC Symbol;Acc:HGNC:18690]"}, {"versioned_ensembl_gene_id":"ENSG00000271134.1","gene_symbol":"AC012498.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60682873,"end":60683244,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214282.3","gene_symbol":"KRT8P14","gene_name":"keratin 8 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:33366]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"347333","summary":null,"start":45632292,"end":45633733,"strand":-1,"description":"keratin 8 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:33366]"}, {"versioned_ensembl_gene_id":"ENSG00000225928.2","gene_symbol":"CACYBPP1","gene_name":"calcyclin binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45122]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420043","summary":null,"start":84454679,"end":84456056,"strand":-1,"description":"calcyclin binding protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45122]"}, {"versioned_ensembl_gene_id":"ENSG00000225423.1","gene_symbol":"TNPO1P1","gene_name":"transportin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45120]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418919","summary":null,"start":84390908,"end":84392045,"strand":1,"description":"transportin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45120]"}, {"versioned_ensembl_gene_id":"ENSG00000107771.15","gene_symbol":"CCSER2","gene_name":"coiled-coil serine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:29197]","synonyms":"KIAA1128,FAM190B","biotype":"protein_coding","ncbi_id":"54462","summary":null,"start":84328586,"end":84518521,"strand":1,"description":"coiled-coil serine rich protein 2 [Source:HGNC Symbol;Acc:HGNC:29197]"}, {"versioned_ensembl_gene_id":"ENSG00000274972.3","gene_symbol":"FRG2","gene_name":"FSHD region gene 2 [Source:HGNC Symbol;Acc:HGNC:19136]","synonyms":"FRG2A","biotype":"protein_coding","ncbi_id":"448831","summary":null,"start":190028329,"end":190031235,"strand":-1,"description":"FSHD region gene 2 [Source:HGNC Symbol;Acc:HGNC:19136]"}, {"versioned_ensembl_gene_id":"ENSG00000261440.1","gene_symbol":"DUX4L45","gene_name":"double homeobox 4 like 45 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51783]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100887074","summary":null,"start":34135736,"end":34136792,"strand":-1,"description":"double homeobox 4 like 45 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51783]"}, {"versioned_ensembl_gene_id":"ENSG00000271555.1","gene_symbol":"AC113139.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":52722903,"end":52723141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260087.1","gene_symbol":"PCMTD1P2","gene_name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38805]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287647","summary":null,"start":34139189,"end":34139543,"strand":1,"description":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38805]"}, {"versioned_ensembl_gene_id":"ENSG00000023287.12","gene_symbol":"RB1CC1","gene_name":"RB1 inducible coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:15574]","synonyms":"ATG17,PPP1R131,KIAA0203,FIP200,DRAGOU14,Cc1","biotype":"protein_coding","ncbi_id":"9821","summary":"The protein encoded by this gene interacts with signaling pathways to coordinately regulate cell growth, cell proliferation, apoptosis, autophagy, and cell migration. This tumor suppressor also enhances retinoblastoma 1 gene expression in cancer cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009]","start":52622456,"end":52745843,"strand":-1,"description":"RB1 inducible coiled-coil 1 [Source:HGNC Symbol;Acc:HGNC:15574]"}, {"versioned_ensembl_gene_id":"ENSG00000232835.1","gene_symbol":"AC107057.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5549780,"end":5556031,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259987.1","gene_symbol":"DUX4L46","gene_name":"double homeobox 4 like 46 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51784]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480349","summary":null,"start":34141256,"end":34142006,"strand":-1,"description":"double homeobox 4 like 46 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51784]"}, {"versioned_ensembl_gene_id":"ENSG00000260207.1","gene_symbol":"DUX4L47","gene_name":"double homeobox 4 like 47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51785]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481738","summary":null,"start":34142456,"end":34142849,"strand":1,"description":"double homeobox 4 like 47 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:51785]"}, {"versioned_ensembl_gene_id":"ENSG00000281310.2","gene_symbol":"AP000351.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24052465,"end":24059615,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256642.1","gene_symbol":"LINC00273","gene_name":"long intergenic non-protein coding RNA 273 [Source:HGNC Symbol;Acc:HGNC:38595]","synonyms":"TOP,NCRNA00273-1,NCRNA00273","biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34158585,"end":34160036,"strand":-1,"description":"long intergenic non-protein coding RNA 273 [Source:HGNC Symbol;Acc:HGNC:38595]"}, {"versioned_ensembl_gene_id":"ENSG00000230090.5","gene_symbol":"AC108025.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":5618327,"end":5691118,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279800.2","gene_symbol":"BCLAF1P2","gene_name":"BCL2 associated transcription factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51807]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"731605","summary":null,"start":34266041,"end":34268649,"strand":-1,"description":"BCL2 associated transcription factor 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51807]"}, {"versioned_ensembl_gene_id":"ENSG00000144671.10","gene_symbol":"SLC22A14","gene_name":"solute carrier family 22 member 14 [Source:HGNC Symbol;Acc:HGNC:8495]","synonyms":"ORCTL4,OCTL2","biotype":"protein_coding","ncbi_id":"9389","summary":"This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":38282294,"end":38318575,"strand":1,"description":"solute carrier family 22 member 14 [Source:HGNC Symbol;Acc:HGNC:8495]"}, {"versioned_ensembl_gene_id":"ENSG00000284209.1","gene_symbol":"FP325313.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":34353616,"end":34371659,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272983.1","gene_symbol":"AL117339.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38137337,"end":38144399,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279165.1","gene_symbol":"AC135776.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":34941977,"end":34943880,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225965.1","gene_symbol":"AL117339.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38161570,"end":38161749,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260722.1","gene_symbol":"VN1R67P","gene_name":"vomeronasal 1 receptor 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:37387]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"100131118","summary":null,"start":31801585,"end":31802497,"strand":-1,"description":"vomeronasal 1 receptor 67 pseudogene [Source:HGNC Symbol;Acc:HGNC:37387]"}, {"versioned_ensembl_gene_id":"ENSG00000224128.1","gene_symbol":"LINC01248","gene_name":"long intergenic non-protein coding RNA 1248 [Source:HGNC Symbol;Acc:HGNC:49842]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"102723818","summary":null,"start":5602505,"end":5691488,"strand":-1,"description":"long intergenic non-protein coding RNA 1248 [Source:HGNC Symbol;Acc:HGNC:49842]"}, {"versioned_ensembl_gene_id":"ENSG00000227013.3","gene_symbol":"OR7E96P","gene_name":"olfactory receptor family 7 subfamily E member 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:14815]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"401450","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":8039978,"end":8040953,"strand":1,"description":"olfactory receptor family 7 subfamily E member 96 pseudogene [Source:HGNC Symbol;Acc:HGNC:14815]"}, {"versioned_ensembl_gene_id":"ENSG00000234059.1","gene_symbol":"CASKP1","gene_name":"calcium/calmodulin dependent serine protein kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1498]","synonyms":"CASKP","biotype":"unprocessed_pseudogene","ncbi_id":"10029","summary":null,"start":12930165,"end":12948182,"strand":-1,"description":"calcium/calmodulin dependent serine protein kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:1498]"}, {"versioned_ensembl_gene_id":"ENSG00000255432.1","gene_symbol":"AP001458.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":62649694,"end":62665178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224035.1","gene_symbol":"SFPQP1","gene_name":"splicing factor proline and glutamine rich pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10775]","synonyms":"SFPQP","biotype":"processed_pseudogene","ncbi_id":"23758","summary":null,"start":13083790,"end":13095805,"strand":1,"description":"splicing factor proline and glutamine rich pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:10775]"}, {"versioned_ensembl_gene_id":"ENSG00000253881.1","gene_symbol":"AC105233.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8048919,"end":8049267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214756.7","gene_symbol":"METTL12","gene_name":"methyltransferase like 12 [Source:HGNC Symbol;Acc:HGNC:33113]","synonyms":"U99HG","biotype":"protein_coding","ncbi_id":"751071","summary":null,"start":62665309,"end":62668496,"strand":1,"description":"methyltransferase like 12 [Source:HGNC Symbol;Acc:HGNC:33113]"}, {"versioned_ensembl_gene_id":"ENSG00000109436.7","gene_symbol":"TBC1D9","gene_name":"TBC1 domain family member 9 [Source:HGNC Symbol;Acc:HGNC:21710]","synonyms":"MDR1,KIAA0882,GRAMD9","biotype":"protein_coding","ncbi_id":"23158","summary":null,"start":140620765,"end":140756120,"strand":-1,"description":"TBC1 domain family member 9 [Source:HGNC Symbol;Acc:HGNC:21710]"}, {"versioned_ensembl_gene_id":"ENSG00000125651.13","gene_symbol":"GTF2F1","gene_name":"general transcription factor IIF subunit 1 [Source:HGNC Symbol;Acc:HGNC:4652]","synonyms":"TFIIF,TF2F1,RAP74,BTF4","biotype":"protein_coding","ncbi_id":"2962","summary":null,"start":6379569,"end":6393981,"strand":-1,"description":"general transcription factor IIF subunit 1 [Source:HGNC Symbol;Acc:HGNC:4652]"}, {"versioned_ensembl_gene_id":"ENSG00000273299.1","gene_symbol":"AC006153.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":90403434,"end":90513391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000221914.9","gene_symbol":"PPP2R2A","gene_name":"protein phosphatase 2 regulatory subunit Balpha [Source:HGNC Symbol;Acc:HGNC:9304]","synonyms":"PR55alpha,PR55A,PR52A,B55alpha,B55A","biotype":"protein_coding","ncbi_id":"5520","summary":"The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes an alpha isoform of the regulatory subunit B55 subfamily. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]","start":26291491,"end":26372680,"strand":1,"description":"protein phosphatase 2 regulatory subunit Balpha [Source:HGNC Symbol;Acc:HGNC:9304]"}, {"versioned_ensembl_gene_id":"ENSG00000251154.1","gene_symbol":"AC002456.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":90469787,"end":90488964,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280440.1","gene_symbol":"AC002064.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":90345873,"end":90346218,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275482.4","gene_symbol":"EPHB6","gene_name":"EPH receptor B6 [Source:HGNC Symbol;Acc:HGNC:3396]","synonyms":"HEP","biotype":"protein_coding","ncbi_id":"2051","summary":"This gene encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins. Unlike other members of this family, the encoded protein does not contain a functional kinase domain. Activity of this protein can influence cell adhesion and migration. Expression of this gene is downregulated during tumor progression, suggesting that the protein may suppress tumor invasion and metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":142916237,"end":142932255,"strand":1,"description":"EPH receptor B6 [Source:HGNC Symbol;Acc:HGNC:3396]"}, {"versioned_ensembl_gene_id":"ENSG00000157224.15","gene_symbol":"CLDN12","gene_name":"claudin 12 [Source:HGNC Symbol;Acc:HGNC:2034]","synonyms":null,"biotype":"protein_coding","ncbi_id":"9069","summary":"This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is expressed in the inner ear and bladder epithelium, and it is over-expressed in colorectal carcinomas. This protein and claudin 2 are critical for vitamin D-dependent Ca2+ absorption between enterocytes. Multiple alternatively spliced transcript variants encoding the same protein have been found.[provided by RefSeq, Sep 2011]","start":90383721,"end":90513402,"strand":1,"description":"claudin 12 [Source:HGNC Symbol;Acc:HGNC:2034]"}, {"versioned_ensembl_gene_id":"ENSG00000233189.1","gene_symbol":"RPL12P29","gene_name":"ribosomal protein L12 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35791]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271274","summary":null,"start":84389170,"end":84389626,"strand":-1,"description":"ribosomal protein L12 pseudogene 29 [Source:HGNC Symbol;Acc:HGNC:35791]"}, {"versioned_ensembl_gene_id":"ENSG00000224987.1","gene_symbol":"AL024507.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107985089,"end":107985690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140263.13","gene_symbol":"SORD","gene_name":"sorbitol dehydrogenase [Source:HGNC Symbol;Acc:HGNC:11184]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6652","summary":"Sorbitol dehydrogenase (SORD; EC 1.1.1.14) catalyzes the interconversion of polyols and their corresponding ketoses, and together with aldose reductase (ALDR1; MIM 103880), makes up the sorbitol pathway that is believed to play an important role in the development of diabetic complications (summarized by Carr and Markham, 1995 [PubMed 8535074]). The first reaction of the pathway (also called the polyol pathway) is the reduction of glucose to sorbitol by ALDR1 with NADPH as the cofactor. SORD then oxidizes the sorbitol to fructose using NAD(+) cofactor.[supplied by OMIM, Jul 2010]","start":45023104,"end":45077185,"strand":1,"description":"sorbitol dehydrogenase [Source:HGNC Symbol;Acc:HGNC:11184]"}, {"versioned_ensembl_gene_id":"ENSG00000112367.10","gene_symbol":"FIG4","gene_name":"FIG4 phosphoinositide 5-phosphatase [Source:HGNC Symbol;Acc:HGNC:16873]","synonyms":"KIAA0274,hSac3,dJ249I4.1,CMT4J,ALS11,SAC3","biotype":"protein_coding","ncbi_id":"9896","summary":"The protein encoded by this gene belongs to the SAC domain-containing protein gene family. The SAC domain, approximately 400 amino acids in length and consisting of seven conserved motifs, has been shown to possess phosphoinositide phosphatase activity. The yeast homolog, Sac1p, is involved in the regulation of various phosphoinositides, and affects diverse cellular functions such as actin cytoskeleton organization, Golgi function, and maintenance of vacuole morphology. Membrane-bound phosphoinositides function as signaling molecules and play a key role in vesicle trafficking in eukaryotic cells. Mutations in this gene have been associated with Charcot-Marie-Tooth disease, type 4J. [provided by RefSeq, Jul 2008]","start":109691312,"end":109825428,"strand":1,"description":"FIG4 phosphoinositide 5-phosphatase [Source:HGNC Symbol;Acc:HGNC:16873]"}, {"versioned_ensembl_gene_id":"ENSG00000280116.2","gene_symbol":"AC231657.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":49155242,"end":49157351,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205857.2","gene_symbol":"NANOGNB","gene_name":"NANOG neighbor homeobox [Source:HGNC Symbol;Acc:HGNC:24958]","synonyms":null,"biotype":"protein_coding","ncbi_id":"360030","summary":null,"start":7765216,"end":7774121,"strand":1,"description":"NANOG neighbor homeobox [Source:HGNC Symbol;Acc:HGNC:24958]"}, {"versioned_ensembl_gene_id":"ENSG00000259250.1","gene_symbol":"AC018904.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58587507,"end":58591676,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282100.1","gene_symbol":"AC091046.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58691106,"end":58693125,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278513.1","gene_symbol":"AC091046.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":58732188,"end":58733149,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137845.14","gene_symbol":"ADAM10","gene_name":"ADAM metallopeptidase domain 10 [Source:HGNC Symbol;Acc:HGNC:188]","synonyms":"MADM,kuz,HsT18717,CD156c","biotype":"protein_coding","ncbi_id":"102","summary":"Members of the ADAM family are cell surface proteins with a unique structure possessing both potential adhesion and protease domains. This gene encodes and ADAM family member that cleaves many proteins including TNF-alpha and E-cadherin. Alternate splicing results in multiple transcript variants encoding different proteins that may undergo similar processing. [provided by RefSeq, Feb 2016]","start":58588807,"end":58749978,"strand":-1,"description":"ADAM metallopeptidase domain 10 [Source:HGNC Symbol;Acc:HGNC:188]"}, {"versioned_ensembl_gene_id":"ENSG00000256192.1","gene_symbol":"AC012158.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64266413,"end":64266766,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250001.1","gene_symbol":"AC027335.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":9519853,"end":9523178,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243024.6","gene_symbol":"AC012158.1","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":64222337,"end":64397065,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000248537.1","gene_symbol":"AC091906.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9363275,"end":9422481,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269313.5","gene_symbol":"MAGIX","gene_name":"MAGI family member, X-linked [Source:HGNC Symbol;Acc:HGNC:30006]","synonyms":"PDZX,JM10,FLJ21687","biotype":"protein_coding","ncbi_id":"79917","summary":null,"start":49162564,"end":49168483,"strand":1,"description":"MAGI family member, X-linked [Source:HGNC Symbol;Acc:HGNC:30006]"}, {"versioned_ensembl_gene_id":"ENSG00000250619.1","gene_symbol":"AC021088.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9001774,"end":9045940,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251370.1","gene_symbol":"SEMA5A-AS1","gene_name":"SEMA5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52973]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929338","summary":null,"start":9511333,"end":9518086,"strand":1,"description":"SEMA5A antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:52973]"}, {"versioned_ensembl_gene_id":"ENSG00000248335.1","gene_symbol":"AC096733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":140712168,"end":140716081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249661.1","gene_symbol":"TNRC18P1","gene_name":"trinucleotide repeat containing 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43881]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644962","summary":null,"start":140641840,"end":140645489,"strand":-1,"description":"trinucleotide repeat containing 18 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43881]"}, {"versioned_ensembl_gene_id":"ENSG00000279698.1","gene_symbol":"AC027335.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":9498401,"end":9498775,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236835.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28896693,"end":28897483,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000180663.5","gene_symbol":"VN1R3","gene_name":"vomeronasal 1 receptor 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19867]","synonyms":"V1RL3,FKSG46","biotype":"unitary_pseudogene","ncbi_id":"317702","summary":null,"start":31807926,"end":31808844,"strand":-1,"description":"vomeronasal 1 receptor 3 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:19867]"}, {"versioned_ensembl_gene_id":"ENSG00000261457.3","gene_symbol":"AC002519.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":31802947,"end":31807973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261284.2","gene_symbol":"RBM22P13","gene_name":"RNA binding motif protein 22 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49208]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130603","summary":null,"start":31863633,"end":31864876,"strand":1,"description":"RNA binding motif protein 22 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:49208]"}, {"versioned_ensembl_gene_id":"ENSG00000259874.1","gene_symbol":"AC034105.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31870887,"end":31871124,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178162.8","gene_symbol":"FAR2P2","gene_name":"fatty acyl-CoA reductase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49279]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100216479","summary":null,"start":130416755,"end":130431363,"strand":-1,"description":"fatty acyl-CoA reductase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49279]"}, {"versioned_ensembl_gene_id":"ENSG00000223617.1","gene_symbol":"LINC00370","gene_name":"long intergenic non-protein coding RNA 370 [Source:HGNC Symbol;Acc:HGNC:42692]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105370357","summary":null,"start":109281973,"end":109287733,"strand":1,"description":"long intergenic non-protein coding RNA 370 [Source:HGNC Symbol;Acc:HGNC:42692]"}, {"versioned_ensembl_gene_id":"ENSG00000185947.14","gene_symbol":"ZNF267","gene_name":"zinc finger protein 267 [Source:HGNC Symbol;Acc:HGNC:13060]","synonyms":"HZF2","biotype":"protein_coding","ncbi_id":"10308","summary":null,"start":31873758,"end":31917357,"strand":1,"description":"zinc finger protein 267 [Source:HGNC Symbol;Acc:HGNC:13060]"}, {"versioned_ensembl_gene_id":"ENSG00000026751.16","gene_symbol":"SLAMF7","gene_name":"SLAM family member 7 [Source:HGNC Symbol;Acc:HGNC:21394]","synonyms":"CS1,CRACC,CD319,19A","biotype":"protein_coding","ncbi_id":"57823","summary":null,"start":160739057,"end":160754821,"strand":1,"description":"SLAM family member 7 [Source:HGNC Symbol;Acc:HGNC:21394]"}, {"versioned_ensembl_gene_id":"ENSG00000236053.1","gene_symbol":"LINC01067","gene_name":"long intergenic non-protein coding RNA 1067 [Source:HGNC Symbol;Acc:HGNC:49105]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107080624","summary":null,"start":109310135,"end":109311773,"strand":1,"description":"long intergenic non-protein coding RNA 1067 [Source:HGNC Symbol;Acc:HGNC:49105]"}, {"versioned_ensembl_gene_id":"ENSG00000233797.1","gene_symbol":"UFL1-AS1","gene_name":"UFL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41007]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100861530","summary":null,"start":96358374,"end":96521669,"strand":-1,"description":"UFL1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41007]"}, {"versioned_ensembl_gene_id":"ENSG00000254398.1","gene_symbol":"AC055876.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28679405,"end":28682252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000014123.9","gene_symbol":"UFL1","gene_name":"UFM1 specific ligase 1 [Source:HGNC Symbol;Acc:HGNC:23039]","synonyms":"RCAD,NLBP,Maxer,KIAA0776","biotype":"protein_coding","ncbi_id":"23376","summary":null,"start":96521595,"end":96555276,"strand":1,"description":"UFM1 specific ligase 1 [Source:HGNC Symbol;Acc:HGNC:23039]"}, {"versioned_ensembl_gene_id":"ENSG00000206149.10","gene_symbol":"HERC2P9","gene_name":"hect domain and RLD 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30495]","synonyms":"FLJ59185","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440248","summary":null,"start":28589492,"end":28685264,"strand":1,"description":"hect domain and RLD 2 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30495]"}, {"versioned_ensembl_gene_id":"ENSG00000255958.1","gene_symbol":"AC115676.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10214161,"end":10214761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000139112.10","gene_symbol":"GABARAPL1","gene_name":"GABA type A receptor associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:4068]","synonyms":"gec1,ATG8L,ATG8B,APG8L","biotype":"protein_coding","ncbi_id":"23710","summary":null,"start":10212458,"end":10223130,"strand":1,"description":"GABA type A receptor associated protein like 1 [Source:HGNC Symbol;Acc:HGNC:4068]"}, {"versioned_ensembl_gene_id":"ENSG00000231112.1","gene_symbol":"MTHFD2P3","gene_name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48866]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481665","summary":null,"start":107985811,"end":107986031,"strand":-1,"description":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:48866]"}, {"versioned_ensembl_gene_id":"ENSG00000213495.3","gene_symbol":"AC012498.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":60711484,"end":60711920,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249814.1","gene_symbol":"RPSAP2","gene_name":"ribosomal protein SA pseudogene 2 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000258334.1","gene_symbol":"AC125611.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":49292631,"end":49324576,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183255.11","gene_symbol":"PTTG1IP","gene_name":"PTTG1 interacting protein [Source:HGNC Symbol;Acc:HGNC:13524]","synonyms":"PBF,C21orf3,C21orf1","biotype":"protein_coding","ncbi_id":"754","summary":"This gene encodes a single-pass type I integral membrane protein, which binds to pituitary tumor-transforming 1 protein (PTTG1), and facilitates translocation of PTTG1 into the nucleus. Coexpression of this protein and PTTG1 induces transcriptional activation of basic fibroblast growth factor. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2013]","start":44849585,"end":44873903,"strand":-1,"description":"PTTG1 interacting protein [Source:HGNC Symbol;Acc:HGNC:13524]"}, {"versioned_ensembl_gene_id":"ENSG00000259950.1","gene_symbol":"AC034105.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31894542,"end":31894983,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273472.1","gene_symbol":"AC096733.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":140756528,"end":140757921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000076258.9","gene_symbol":"FMO4","gene_name":"flavin containing monooxygenase 4 [Source:HGNC Symbol;Acc:HGNC:3772]","synonyms":"FMO2","biotype":"protein_coding","ncbi_id":"2329","summary":"Metabolic N-oxidation of diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man. This results in a small subpopulation with reduced TMA N-oxidation capacity and causes fish odor syndrome (Trimethylaminuria). Three forms of the enzyme are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. [provided by RefSeq, Jan 2015]","start":171314208,"end":171342084,"strand":1,"description":"flavin containing monooxygenase 4 [Source:HGNC Symbol;Acc:HGNC:3772]"}, {"versioned_ensembl_gene_id":"ENSG00000135406.13","gene_symbol":"PRPH","gene_name":"peripherin [Source:HGNC Symbol;Acc:HGNC:9461]","synonyms":"PRPH1,NEF4","biotype":"protein_coding","ncbi_id":"5630","summary":"This gene encodes a cytoskeletal protein found in neurons of the peripheral nervous system. The encoded protein is a type III intermediate filament protein with homology to other cytoskeletal proteins such as desmin, and is a different protein that the peripherin found in photoreceptors. Mutations in this gene have been associated with susceptibility to amyotrophic lateral sclerosis. [provided by RefSeq, Jul 2008]","start":49293252,"end":49298686,"strand":1,"description":"peripherin [Source:HGNC Symbol;Acc:HGNC:9461]"}, {"versioned_ensembl_gene_id":"ENSG00000140367.11","gene_symbol":"UBE2Q2","gene_name":"ubiquitin conjugating enzyme E2 Q2 [Source:HGNC Symbol;Acc:HGNC:19248]","synonyms":"DKFZp762C143","biotype":"protein_coding","ncbi_id":"92912","summary":null,"start":75843285,"end":75901078,"strand":1,"description":"ubiquitin conjugating enzyme E2 Q2 [Source:HGNC Symbol;Acc:HGNC:19248]"}, {"versioned_ensembl_gene_id":"ENSG00000170153.10","gene_symbol":"RNF150","gene_name":"ring finger protein 150 [Source:HGNC Symbol;Acc:HGNC:23138]","synonyms":"KIAA1214","biotype":"protein_coding","ncbi_id":"57484","summary":null,"start":140859807,"end":141212877,"strand":-1,"description":"ring finger protein 150 [Source:HGNC Symbol;Acc:HGNC:23138]"}, {"versioned_ensembl_gene_id":"ENSG00000259352.1","gene_symbol":"AC091117.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45073492,"end":45074048,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259418.1","gene_symbol":"AC091117.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45041716,"end":45058707,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238126.1","gene_symbol":"UQCRHP1","gene_name":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]","synonyms":"UQCRHP5,Em:AF129756.18","biotype":"processed_pseudogene","ncbi_id":"100130756","summary":null,"start":31678099,"end":31678372,"strand":-1,"description":"ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31341]"}, {"versioned_ensembl_gene_id":"ENSG00000228653.2","gene_symbol":"HNRNPCP7","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48818]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127907","summary":null,"start":64500825,"end":64501729,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:48818]"}, {"versioned_ensembl_gene_id":"ENSG00000262020.1","gene_symbol":"AC007014.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11066496,"end":11071102,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229917.2","gene_symbol":"RPL7P46","gene_name":"ribosomal protein L7 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36706]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642451","summary":null,"start":11027024,"end":11027763,"strand":1,"description":"ribosomal protein L7 pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:36706]"}, {"versioned_ensembl_gene_id":"ENSG00000211751.9","gene_symbol":"AC245427.1","gene_name":null,"synonyms":null,"biotype":"TR_C_gene","ncbi_id":null,"summary":null,"start":142791694,"end":142793368,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137309.19","gene_symbol":"HMGA1","gene_name":"high mobility group AT-hook 1 [Source:HGNC Symbol;Acc:HGNC:5010]","synonyms":"HMGIY","biotype":"protein_coding","ncbi_id":"3159","summary":"This gene encodes a chromatin-associated protein involved in the regulation of gene transcription, integration of retroviruses into chromosomes, and the metastatic progression of cancer cells. The encoded protein preferentially binds to the minor groove of AT-rich regions in double-stranded DNA. Multiple transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene have been identified on multiple chromosomes. [provided by RefSeq, Jan 2016]","start":34236873,"end":34246231,"strand":1,"description":"high mobility group AT-hook 1 [Source:HGNC Symbol;Acc:HGNC:5010]"}, {"versioned_ensembl_gene_id":"ENSG00000211764.1","gene_symbol":"TRBJ2-1","gene_name":"T-cell receptor beta joining 2-1 [Source:HGNC Symbol;Acc:HGNC:12168]","synonyms":"TRBJ21,TCRBJ2S1","biotype":"TR_J_gene","ncbi_id":"28629","summary":null,"start":142796365,"end":142796414,"strand":1,"description":"T-cell receptor beta joining 2-1 [Source:HGNC Symbol;Acc:HGNC:12168]"}, {"versioned_ensembl_gene_id":"ENSG00000239402.3","gene_symbol":"CYP4F62P","gene_name":"cytochrome P450 family 4 subfamily F member 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:39956]","synonyms":"CYP4F43P,CYP4F-se11[6:7:8]","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"646802","summary":null,"start":130429827,"end":130441413,"strand":-1,"description":"cytochrome P450 family 4 subfamily F member 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:39956]"}, {"versioned_ensembl_gene_id":"ENSG00000270935.1","gene_symbol":"AL021808.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27268113,"end":27269229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223974.1","gene_symbol":"BNIP3P42","gene_name":"BCL2 interacting protein 3 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:49722]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481697","summary":null,"start":64551498,"end":64552066,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:49722]"}, {"versioned_ensembl_gene_id":"ENSG00000173041.11","gene_symbol":"ZNF680","gene_name":"zinc finger protein 680 [Source:HGNC Symbol;Acc:HGNC:26897]","synonyms":"FLJ90430","biotype":"protein_coding","ncbi_id":"340252","summary":null,"start":64519884,"end":64563106,"strand":-1,"description":"zinc finger protein 680 [Source:HGNC Symbol;Acc:HGNC:26897]"}, {"versioned_ensembl_gene_id":"ENSG00000211765.1","gene_symbol":"TRBJ2-2","gene_name":"T-cell receptor beta joining 2-2 [Source:HGNC Symbol;Acc:HGNC:12169]","synonyms":"TRBJ22,TCRBJ2S2","biotype":"TR_J_gene","ncbi_id":"28628","summary":null,"start":142796560,"end":142796610,"strand":1,"description":"T-cell receptor beta joining 2-2 [Source:HGNC Symbol;Acc:HGNC:12169]"}, {"versioned_ensembl_gene_id":"ENSG00000158553.4","gene_symbol":"POM121L2","gene_name":"POM121 transmembrane nucleoporin like 2 [Source:HGNC Symbol;Acc:HGNC:13973]","synonyms":"POM121-L","biotype":"protein_coding","ncbi_id":"94026","summary":null,"start":27285903,"end":27312170,"strand":-1,"description":"POM121 transmembrane nucleoporin like 2 [Source:HGNC Symbol;Acc:HGNC:13973]"}, {"versioned_ensembl_gene_id":"ENSG00000230646.1","gene_symbol":"KLF2P2","gene_name":"Kruppel like factor 2 pseudogene 2 [Source:HGNC 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Symbol;Acc:HGNC:12170]","synonyms":"TRBJ22P","biotype":"TR_J_gene","ncbi_id":"28627","summary":null,"start":142796697,"end":142796742,"strand":1,"description":"T-cell receptor beta joining 2-2P (non-functional) [Source:HGNC Symbol;Acc:HGNC:12170]"}, {"versioned_ensembl_gene_id":"ENSG00000203506.5","gene_symbol":"RBMS3-AS2","gene_name":"RBMS3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39988]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873978","summary":null,"start":29526251,"end":29642809,"strand":-1,"description":"RBMS3 antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:39988]"}, {"versioned_ensembl_gene_id":"ENSG00000211767.1","gene_symbol":"TRBJ2-3","gene_name":"T-cell receptor beta joining 2-3 [Source:HGNC Symbol;Acc:HGNC:12171]","synonyms":"TRBJ23,TCRBJ2S3","biotype":"TR_J_gene","ncbi_id":"28626","summary":null,"start":142796847,"end":142796895,"strand":1,"description":"T-cell receptor beta joining 2-3 [Source:HGNC Symbol;Acc:HGNC:12171]"}, {"versioned_ensembl_gene_id":"ENSG00000220758.4","gene_symbol":"VN1R10P","gene_name":"vomeronasal 1 receptor 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:13550]","synonyms":"VNR6I1P,hs6V1-1p,b24o18.2","biotype":"unprocessed_pseudogene","ncbi_id":"387316","summary":null,"start":27324894,"end":27325768,"strand":1,"description":"vomeronasal 1 receptor 10 pseudogene [Source:HGNC Symbol;Acc:HGNC:13550]"}, {"versioned_ensembl_gene_id":"ENSG00000255571.8","gene_symbol":"MIR9-3HG","gene_name":"MIR9-3 host gene [Source:HGNC Symbol;Acc:HGNC:27388]","synonyms":"LINC00925","biotype":"lincRNA","ncbi_id":"254559","summary":null,"start":89361579,"end":89398487,"strand":1,"description":"MIR9-3 host gene [Source:HGNC Symbol;Acc:HGNC:27388]"}, {"versioned_ensembl_gene_id":"ENSG00000226216.1","gene_symbol":"RPS12P5","gene_name":"ribosomal protein S12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36525]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271053","summary":null,"start":29390848,"end":29391218,"strand":1,"description":"ribosomal protein S12 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:36525]"}, {"versioned_ensembl_gene_id":"ENSG00000111704.10","gene_symbol":"NANOG","gene_name":"Nanog homeobox [Source:HGNC Symbol;Acc:HGNC:20857]","synonyms":"FLJ40451,FLJ12581","biotype":"protein_coding","ncbi_id":"79923","summary":"The protein encoded by this gene is a DNA binding homeobox transcription factor involved in embryonic stem (ES) cell proliferation, renewal, and pluripotency. The encoded protein can block ES cell differentiation and can also autorepress its own expression in differentiating cells. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]","start":7787794,"end":7799141,"strand":1,"description":"Nanog homeobox [Source:HGNC Symbol;Acc:HGNC:20857]"}, {"versioned_ensembl_gene_id":"ENSG00000211768.1","gene_symbol":"TRBJ2-4","gene_name":"T-cell receptor beta joining 2-4 [Source:HGNC Symbol;Acc:HGNC:12172]","synonyms":"TRBJ24,TCRBJ2S4","biotype":"TR_J_gene","ncbi_id":"28625","summary":null,"start":142796998,"end":142797047,"strand":1,"description":"T-cell receptor beta joining 2-4 [Source:HGNC Symbol;Acc:HGNC:12172]"}, {"versioned_ensembl_gene_id":"ENSG00000235904.2","gene_symbol":"RBMS3-AS3","gene_name":"RBMS3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:39989]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873979","summary":null,"start":29264194,"end":29290726,"strand":-1,"description":"RBMS3 antisense RNA 3 [Source:HGNC Symbol;Acc:HGNC:39989]"}, {"versioned_ensembl_gene_id":"ENSG00000211769.1","gene_symbol":"TRBJ2-5","gene_name":"T-cell receptor beta joining 2-5 [Source:HGNC Symbol;Acc:HGNC:12173]","synonyms":"TCRBJ2S5,TRBJ25","biotype":"TR_J_gene","ncbi_id":"28624","summary":null,"start":142797119,"end":142797166,"strand":1,"description":"T-cell receptor beta joining 2-5 [Source:HGNC Symbol;Acc:HGNC:12173]"}, {"versioned_ensembl_gene_id":"ENSG00000227795.1","gene_symbol":"MTND4LP9","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42243]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075237","summary":null,"start":29797652,"end":29797825,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42243]"}, {"versioned_ensembl_gene_id":"ENSG00000211770.1","gene_symbol":"TRBJ2-6","gene_name":"T-cell receptor beta joining 2-6 [Source:HGNC Symbol;Acc:HGNC:12174]","synonyms":"TRBJ26,TCRBJ2S6","biotype":"TR_J_gene","ncbi_id":"28623","summary":null,"start":142797239,"end":142797291,"strand":1,"description":"T-cell receptor beta joining 2-6 [Source:HGNC Symbol;Acc:HGNC:12174]"}, {"versioned_ensembl_gene_id":"ENSG00000230480.1","gene_symbol":"AC093142.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28447725,"end":28448073,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276667.1","gene_symbol":"AL158077.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":19895800,"end":19895973,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206559.7","gene_symbol":"ZCWPW2","gene_name":"zinc finger CW-type and PWWP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23574]","synonyms":"ZCW2","biotype":"protein_coding","ncbi_id":"152098","summary":null,"start":28349146,"end":28538122,"strand":1,"description":"zinc finger CW-type and PWWP domain containing 2 [Source:HGNC Symbol;Acc:HGNC:23574]"}, {"versioned_ensembl_gene_id":"ENSG00000204789.4","gene_symbol":"ZNF204P","gene_name":"zinc finger protein 204, pseudogene [Source:HGNC Symbol;Acc:HGNC:12995]","synonyms":"ZNF315P,ZNF204,ZNF184-Lp,b24o18.1","biotype":"processed_pseudogene","ncbi_id":"7754","summary":"This locus represents a transcribed pseudogene, possibly of ZNF79 (GeneID 7633). 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[provided by RefSeq, Jun 2011]","start":27357825,"end":27360221,"strand":-1,"description":"zinc finger protein 204, pseudogene [Source:HGNC Symbol;Acc:HGNC:12995]"}, {"versioned_ensembl_gene_id":"ENSG00000261402.1","gene_symbol":"AL591222.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19926094,"end":19929937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182625.3","gene_symbol":"AC091046.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58686411,"end":58686617,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269444.1","gene_symbol":"AC011491.2","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":6386762,"end":6390400,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270986.1","gene_symbol":"HMGB1P51","gene_name":"high mobility group box 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:52369]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"109729159","summary":null,"start":58672296,"end":58672933,"strand":1,"description":"high mobility group box 1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:52369]"}, {"versioned_ensembl_gene_id":"ENSG00000211771.1","gene_symbol":"TRBJ2-7","gene_name":"T-cell receptor beta joining 2-7 [Source:HGNC Symbol;Acc:HGNC:12175]","synonyms":"TRBJ27,TCRBJ2S7","biotype":"TR_J_gene","ncbi_id":"28622","summary":null,"start":142797456,"end":142797502,"strand":1,"description":"T-cell receptor beta joining 2-7 [Source:HGNC Symbol;Acc:HGNC:12175]"}, {"versioned_ensembl_gene_id":"ENSG00000262492.1","gene_symbol":"AC104581.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7954868,"end":7955622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214347.7","gene_symbol":"AC011491.1","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":6393809,"end":6412404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271707.1","gene_symbol":"ATP1B3P1","gene_name":"ATPase Na+/K+ transporting subunit beta 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:807]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"484","summary":null,"start":60734895,"end":60735715,"strand":-1,"description":"ATPase Na+/K+ transporting subunit beta 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:807]"}, {"versioned_ensembl_gene_id":"ENSG00000242292.2","gene_symbol":"AC010631.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":36588506,"end":36588661,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000211772.11","gene_symbol":"TRBC2","gene_name":"T-cell receptor beta constant 2 [Source:HGNC Symbol;Acc:HGNC:12157]","synonyms":"TCRBC2","biotype":"TR_C_gene","ncbi_id":"28638","summary":null,"start":142801041,"end":142802748,"strand":1,"description":"T-cell receptor beta constant 2 [Source:HGNC Symbol;Acc:HGNC:12157]"}, {"versioned_ensembl_gene_id":"ENSG00000230574.1","gene_symbol":"NOP56P1","gene_name":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]","synonyms":"NOL5B,NOP56-L,dJ207F6.1,NOL5BP","biotype":"processed_pseudogene","ncbi_id":"646192","summary":null,"start":28784450,"end":28784821,"strand":-1,"description":"NOP56 ribonucleoprotein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13962]"}, {"versioned_ensembl_gene_id":"ENSG00000270712.1","gene_symbol":"AL591222.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19957394,"end":19958147,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237006.1","gene_symbol":"AL669978.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":28838507,"end":28839644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277711.1","gene_symbol":"AL591222.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19967239,"end":19967994,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237254.2","gene_symbol":"TRBV30","gene_name":"T-cell receptor beta variable 30 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12214]","synonyms":"TCRBV30S1,TCRBV20S1A1N2","biotype":"TR_V_gene","ncbi_id":"28557","summary":null,"start":142812586,"end":142813399,"strand":-1,"description":"T-cell receptor beta variable 30 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:12214]"}, {"versioned_ensembl_gene_id":"ENSG00000226714.1","gene_symbol":"AL669978.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28862047,"end":28862678,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237434.1","gene_symbol":"AL512635.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20331446,"end":20332277,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227966.1","gene_symbol":"LINC01623","gene_name":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"401242","summary":null,"start":28860261,"end":28864009,"strand":-1,"description":"long intergenic non-protein coding RNA 1623 [Source:HGNC Symbol;Acc:HGNC:52050]"}, {"versioned_ensembl_gene_id":"ENSG00000283312.1","gene_symbol":"AC017104.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231493708,"end":231495299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260854.1","gene_symbol":"LINC02184","gene_name":"long intergenic non-protein coding RNA 2184 [Source:HGNC Symbol;Acc:HGNC:53046]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505948","summary":null,"start":34978744,"end":34979844,"strand":-1,"description":"long intergenic non-protein coding RNA 2184 [Source:HGNC Symbol;Acc:HGNC:53046]"}, {"versioned_ensembl_gene_id":"ENSG00000124613.8","gene_symbol":"ZNF391","gene_name":"zinc finger protein 391 [Source:HGNC Symbol;Acc:HGNC:18779]","synonyms":"dJ153G14.3","biotype":"protein_coding","ncbi_id":"346157","summary":null,"start":27374615,"end":27403904,"strand":1,"description":"zinc finger protein 391 [Source:HGNC Symbol;Acc:HGNC:18779]"}, {"versioned_ensembl_gene_id":"ENSG00000233940.1","gene_symbol":"RPL12P45","gene_name":"ribosomal protein L12 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:51937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419477","summary":null,"start":35053468,"end":35059271,"strand":1,"description":"ribosomal protein L12 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:51937]"}, {"versioned_ensembl_gene_id":"ENSG00000262885.1","gene_symbol":"AC135776.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35023339,"end":35023765,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276289.4","gene_symbol":"KCNE1B","gene_name":"potassium voltage-gated channel subfamily E regulatory subunit 1B [Source:HGNC Symbol;Acc:HGNC:52280]","synonyms":null,"biotype":"protein_coding","ncbi_id":"102723475","summary":null,"start":7816675,"end":7829926,"strand":-1,"description":"potassium voltage-gated channel subfamily E regulatory subunit 1B [Source:HGNC Symbol;Acc:HGNC:52280]"}, {"versioned_ensembl_gene_id":"ENSG00000179755.3","gene_symbol":"AC135776.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35021749,"end":35024229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000081087.14","gene_symbol":"OSTM1","gene_name":"osteopetrosis associated transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:21652]","synonyms":"HSPC019,GL","biotype":"protein_coding","ncbi_id":"28962","summary":"This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis. [provided by RefSeq, Jul 2008]","start":108041409,"end":108165854,"strand":-1,"description":"osteopetrosis associated transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:21652]"}, {"versioned_ensembl_gene_id":"ENSG00000226254.1","gene_symbol":"PTP4A1P3","gene_name":"protein tyrosine phosphatase type IVA, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41930]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100861469","summary":null,"start":91107374,"end":91107793,"strand":1,"description":"protein tyrosine phosphatase type IVA, member 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:41930]"}, {"versioned_ensembl_gene_id":"ENSG00000058091.16","gene_symbol":"CDK14","gene_name":"cyclin dependent kinase 14 [Source:HGNC Symbol;Acc:HGNC:8883]","synonyms":"PFTK1,PFTAIRE1","biotype":"protein_coding","ncbi_id":"5218","summary":"PFTK1 is a member of the CDC2 (MIM 116940)-related protein kinase family (Yang and Chen, 2001 [PubMed 11313143]).[supplied by OMIM, Mar 2008]","start":90466424,"end":91210590,"strand":1,"description":"cyclin dependent kinase 14 [Source:HGNC Symbol;Acc:HGNC:8883]"}, {"versioned_ensembl_gene_id":"ENSG00000186787.8","gene_symbol":"SPIN2B","gene_name":"spindlin family member 2B [Source:HGNC Symbol;Acc:HGNC:33147]","synonyms":"TDRD26,SPIN-2","biotype":"protein_coding","ncbi_id":"474343","summary":null,"start":57118551,"end":57121546,"strand":-1,"description":"spindlin family member 2B [Source:HGNC Symbol;Acc:HGNC:33147]"}, {"versioned_ensembl_gene_id":"ENSG00000280389.1","gene_symbol":"AC048338.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":122255119,"end":122260274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278138.2","gene_symbol":"CLUHP11","gene_name":"clustered mitochondria homolog pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51806]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100418756","summary":null,"start":35068211,"end":35085060,"strand":1,"description":"clustered mitochondria homolog pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:51806]"}, {"versioned_ensembl_gene_id":"ENSG00000216671.6","gene_symbol":"CCNYL3","gene_name":"cyclin Y-like 3 [Source:HGNC Symbol;Acc:HGNC:33206]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"102724928","summary":null,"start":35040164,"end":35084313,"strand":1,"description":"cyclin Y-like 3 [Source:HGNC Symbol;Acc:HGNC:33206]"}, {"versioned_ensembl_gene_id":"ENSG00000274080.1","gene_symbol":"AC005089.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":73609262,"end":73611502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000009950.15","gene_symbol":"MLXIPL","gene_name":"MLX interacting protein like [Source:HGNC Symbol;Acc:HGNC:12744]","synonyms":"bHLHd14,WS-bHLH,WBSCR14,MONDOB,MIO,CHREBP","biotype":"protein_coding","ncbi_id":"51085","summary":"This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]","start":73593194,"end":73624543,"strand":-1,"description":"MLX interacting protein like [Source:HGNC Symbol;Acc:HGNC:12744]"}, {"versioned_ensembl_gene_id":"ENSG00000271755.1","gene_symbol":"AL031118.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":27404010,"end":27406964,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278531.1","gene_symbol":"AL512324.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":45187292,"end":45198323,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237154.2","gene_symbol":"MCFD2P1","gene_name":"multiple coagulation factor deficiency 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21582]","synonyms":"C6orf44,NUCB2-L,MCFD2L,dJ153G14.2","biotype":"processed_pseudogene","ncbi_id":"645927","summary":null,"start":27407697,"end":27407996,"strand":1,"description":"multiple coagulation factor deficiency 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:21582]"}, {"versioned_ensembl_gene_id":"ENSG00000280940.1","gene_symbol":"AP000351.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":24060497,"end":24062557,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096654.15","gene_symbol":"ZNF184","gene_name":"zinc finger protein 184 [Source:HGNC Symbol;Acc:HGNC:12975]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7738","summary":"The protein encoded by this gene is predicted to be a Kruppel C2H2-type zinc-finger protein family member. Sequence analysis predicts that the protein contains two Kruppel associated box (KRAB) boxes in the N-terminus and highly conserved zinc finger motifs at the C-terminus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]","start":27450743,"end":27473118,"strand":-1,"description":"zinc finger protein 184 [Source:HGNC Symbol;Acc:HGNC:12975]"}, {"versioned_ensembl_gene_id":"ENSG00000274000.4","gene_symbol":"LILRA2","gene_name":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]","synonyms":"LIR-7,ILT1,CD85h,LIR7","biotype":"protein_coding","ncbi_id":"11027","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]","start":54504943,"end":54519583,"strand":1,"description":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]"}, {"versioned_ensembl_gene_id":"ENSG00000278961.1","gene_symbol":"CU633980.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7788703,"end":7793954,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000096088.16","gene_symbol":"PGC","gene_name":"progastricsin [Source:HGNC Symbol;Acc:HGNC:8890]","synonyms":null,"biotype":"protein_coding","ncbi_id":"5225","summary":"This gene encodes an aspartic proteinase that belongs to the peptidase family A1. The encoded protein is a digestive enzyme that is produced in the stomach and constitutes a major component of the gastric mucosa. This protein is also secreted into the serum. This protein is synthesized as an inactive zymogen that includes a highly basic prosegment. This enzyme is converted into its active mature form at low pH by sequential cleavage of the prosegment that is carried out by the enzyme itself. Polymorphisms in this gene are associated with susceptibility to gastric cancers. Serum levels of this enzyme are used as a biomarker for certain gastric diseases including Helicobacter pylori related gastritis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 1. [provided by RefSeq, Oct 2009]","start":41736711,"end":41754109,"strand":-1,"description":"progastricsin [Source:HGNC Symbol;Acc:HGNC:8890]"}, {"versioned_ensembl_gene_id":"ENSG00000279967.1","gene_symbol":"FP671120.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8101251,"end":8103706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260628.5","gene_symbol":"AC142381.3","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":31975803,"end":32003728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284661.1","gene_symbol":"AC105233.6","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8065599,"end":8065816,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253893.2","gene_symbol":"FAM85B","gene_name":"family with sequence similarity 85 member B [Source:HGNC Symbol;Acc:HGNC:32160]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105379219","summary":null,"start":8167819,"end":8226614,"strand":-1,"description":"family with sequence similarity 85 member B [Source:HGNC Symbol;Acc:HGNC:32160]"}, {"versioned_ensembl_gene_id":"ENSG00000258444.1","gene_symbol":"AL132855.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23415339,"end":23415686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258369.1","gene_symbol":"ADI1P3","gene_name":"acireductone dioxygenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52341]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100288129","summary":null,"start":47463087,"end":47463621,"strand":1,"description":"acireductone dioxygenase 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:52341]"}, {"versioned_ensembl_gene_id":"ENSG00000090316.15","gene_symbol":"MAEA","gene_name":"macrophage erythroblast attacher [Source:HGNC Symbol;Acc:HGNC:13731]","synonyms":"GID9,EMP","biotype":"protein_coding","ncbi_id":"10296","summary":"This gene encodes a protein that mediates the attachment of erythroblasts to macrophages. This attachment promotes terminal maturation and enucleation of erythroblasts, presumably by suppressing apoptosis. The encoded protein is an integral membrane protein with the N-terminus on the extracellular side and the C-terminus on the cytoplasmic side of the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":1289851,"end":1340147,"strand":1,"description":"macrophage erythroblast attacher [Source:HGNC Symbol;Acc:HGNC:13731]"}, {"versioned_ensembl_gene_id":"ENSG00000008405.11","gene_symbol":"CRY1","gene_name":"cryptochrome circadian clock 1 [Source:HGNC Symbol;Acc:HGNC:2384]","synonyms":"PHLL1","biotype":"protein_coding","ncbi_id":"1407","summary":"This gene encodes a flavin adenine dinucleotide-binding protein that is a key component of the circadian core oscillator complex, which regulates the circadian clock. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene have been associated with altered sleep patterns. The encoded protein is widely conserved across plants and animals. Loss of the related gene in mouse results in a shortened circadian cycle in complete darkness. [provided by RefSeq, Jan 2014]","start":106991364,"end":107093829,"strand":-1,"description":"cryptochrome circadian clock 1 [Source:HGNC Symbol;Acc:HGNC:2384]"}, {"versioned_ensembl_gene_id":"ENSG00000092054.12","gene_symbol":"MYH7","gene_name":"myosin heavy chain 7 [Source:HGNC Symbol;Acc:HGNC:7577]","synonyms":"MPD1,CMH1,CMD1S","biotype":"protein_coding","ncbi_id":"4625","summary":"Muscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy. [provided by RefSeq, Jul 2008]","start":23412738,"end":23435718,"strand":-1,"description":"myosin heavy chain 7 [Source:HGNC Symbol;Acc:HGNC:7577]"}, {"versioned_ensembl_gene_id":"ENSG00000249188.1","gene_symbol":"ENPP7P1","gene_name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48699]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100421823","summary":null,"start":8154308,"end":8216916,"strand":1,"description":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48699]"}, {"versioned_ensembl_gene_id":"ENSG00000136280.15","gene_symbol":"CCM2","gene_name":"CCM2 scaffolding protein [Source:HGNC Symbol;Acc:HGNC:21708]","synonyms":"OSM,MGC4607,C7orf22","biotype":"protein_coding","ncbi_id":"83605","summary":"This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]","start":44999475,"end":45076469,"strand":1,"description":"CCM2 scaffolding protein [Source:HGNC Symbol;Acc:HGNC:21708]"}, {"versioned_ensembl_gene_id":"ENSG00000244427.1","gene_symbol":"AC105233.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8095946,"end":8096726,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284606.1","gene_symbol":"AC105233.5","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":8059572,"end":8199973,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234048.1","gene_symbol":"FAM96AP1","gene_name":"family with sequence similarity 96 member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43861]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480777","summary":null,"start":28427963,"end":28428444,"strand":-1,"description":"family with sequence similarity 96 member A pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43861]"}, {"versioned_ensembl_gene_id":"ENSG00000255459.1","gene_symbol":"AC105233.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8086022,"end":8086765,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284603.1","gene_symbol":"AC105233.4","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8059459,"end":8059674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137947.11","gene_symbol":"GTF2B","gene_name":"general transcription factor IIB [Source:HGNC Symbol;Acc:HGNC:4648]","synonyms":"TFIIB","biotype":"protein_coding","ncbi_id":"2959","summary":"This gene encodes the general transcription factor IIB, one of the ubiquitous factors required for transcription initiation by RNA polymerase II. The protein localizes to the nucleus where it forms a complex (the DAB complex) with transcription factors IID and IIA. Transcription factor IIB serves as a bridge between IID, the factor which initially recognizes the promoter sequence, and RNA polymerase II. [provided by RefSeq, Jul 2008]","start":88852932,"end":88891944,"strand":-1,"description":"general transcription factor IIB [Source:HGNC Symbol;Acc:HGNC:4648]"}, {"versioned_ensembl_gene_id":"ENSG00000235349.1","gene_symbol":"AC016769.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64566814,"end":64567443,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233585.1","gene_symbol":"AC231533.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48775993,"end":48776970,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268955.2","gene_symbol":"AC068020.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8188535,"end":8189195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254311.1","gene_symbol":"SNRPCP17","gene_name":"small nuclear ribonucleoprotein polypeptide C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49832]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481702","summary":null,"start":8116745,"end":8116949,"strand":-1,"description":"small nuclear ribonucleoprotein polypeptide C pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:49832]"}, {"versioned_ensembl_gene_id":"ENSG00000117305.14","gene_symbol":"HMGCL","gene_name":"3-hydroxymethyl-3-methylglutaryl-CoA lyase [Source:HGNC Symbol;Acc:HGNC:5005]","synonyms":"HL","biotype":"protein_coding","ncbi_id":"3155","summary":"The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]","start":23801885,"end":23838620,"strand":-1,"description":"3-hydroxymethyl-3-methylglutaryl-CoA lyase [Source:HGNC Symbol;Acc:HGNC:5005]"}, {"versioned_ensembl_gene_id":"ENSG00000235462.1","gene_symbol":"TAB3P1","gene_name":"TGF-beta activated kinase 1/MAP3K7 binding protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37723]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"643199","summary":null,"start":13153931,"end":13162214,"strand":-1,"description":"TGF-beta activated kinase 1/MAP3K7 binding protein 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37723]"}, {"versioned_ensembl_gene_id":"ENSG00000174028.6","gene_symbol":"FAM3C2","gene_name":"family with sequence similarity 3 member C2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34501]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286460","summary":null,"start":23075758,"end":23076767,"strand":1,"description":"family with sequence similarity 3 member C2 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:34501]"}, {"versioned_ensembl_gene_id":"ENSG00000223915.1","gene_symbol":"DPPA2P1","gene_name":"developmental pluripotency associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38448]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421137","summary":null,"start":13230884,"end":13231439,"strand":1,"description":"developmental pluripotency associated 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:38448]"}, {"versioned_ensembl_gene_id":"ENSG00000231846.1","gene_symbol":"AC092832.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22428132,"end":22494713,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279174.1","gene_symbol":"AC104581.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":8013327,"end":8016378,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102145.13","gene_symbol":"GATA1","gene_name":"GATA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4170]","synonyms":"NFE1,NF-E1,GF1,GATA-1,ERYF1","biotype":"protein_coding","ncbi_id":"2623","summary":"This gene encodes a protein which belongs to the GATA family of transcription factors. The protein plays an important role in erythroid development by regulating the switch of fetal hemoglobin to adult hemoglobin. Mutations in this gene have been associated with X-linked dyserythropoietic anemia and thrombocytopenia. [provided by RefSeq, Jul 2008]","start":48786554,"end":48794311,"strand":1,"description":"GATA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4170]"}, {"versioned_ensembl_gene_id":"ENSG00000132518.6","gene_symbol":"GUCY2D","gene_name":"guanylate cyclase 2D, retinal [Source:HGNC Symbol;Acc:HGNC:4689]","synonyms":"LCA1,LCA,GUC2D,GUC1A4,CYGD,CORD6,ROS-GC1,RETGC-1,retGC","biotype":"protein_coding","ncbi_id":"3000","summary":"This gene encodes a retina-specific guanylate cyclase, which is a member of the membrane guanylyl cyclase family. Like other membrane guanylyl cyclases, this enzyme has a hydrophobic amino-terminal signal sequence followed by a large extracellular domain, a single membrane spanning domain, a kinase homology domain, and a guanylyl cyclase catalytic domain. In contrast to other membrane guanylyl cyclases, this enzyme is not activated by natriuretic peptides. Mutations in this gene result in Leber congenital amaurosis and cone-rod dystrophy-6 diseases. [provided by RefSeq, Dec 2008]","start":8002594,"end":8020339,"strand":1,"description":"guanylate cyclase 2D, retinal [Source:HGNC Symbol;Acc:HGNC:4689]"}, {"versioned_ensembl_gene_id":"ENSG00000204178.9","gene_symbol":"TMEM57","gene_name":"transmembrane protein 57 [Source:HGNC Symbol;Acc:HGNC:25572]","synonyms":"FLJ10747","biotype":"protein_coding","ncbi_id":"55219","summary":null,"start":25430858,"end":25500209,"strand":1,"description":"transmembrane protein 57 [Source:HGNC Symbol;Acc:HGNC:25572]"}, {"versioned_ensembl_gene_id":"ENSG00000242540.2","gene_symbol":"AC108025.2","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":5696220,"end":5708095,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260218.1","gene_symbol":"AC034105.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31963803,"end":31964079,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228610.1","gene_symbol":"PDCL2P1","gene_name":"phosducin-like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50340]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"653707","summary":null,"start":23198339,"end":23198690,"strand":1,"description":"phosducin-like 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:50340]"}, {"versioned_ensembl_gene_id":"ENSG00000261727.2","gene_symbol":"AC142381.4","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32008438,"end":32084785,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176887.6","gene_symbol":"SOX11","gene_name":"SRY-box 11 [Source:HGNC Symbol;Acc:HGNC:11191]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6664","summary":"This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The protein may function in the developing nervous system and play a role in tumorigenesis. [provided by RefSeq, Jul 2008]","start":5692667,"end":5701385,"strand":1,"description":"SRY-box 11 [Source:HGNC Symbol;Acc:HGNC:11191]"}, {"versioned_ensembl_gene_id":"ENSG00000224396.1","gene_symbol":"METTL15P3","gene_name":"methyltransferase like 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39558]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729650","summary":null,"start":22435598,"end":22436818,"strand":1,"description":"methyltransferase like 15 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39558]"}, {"versioned_ensembl_gene_id":"ENSG00000270472.2","gene_symbol":"IGHV3OR16-9","gene_name":"immunoglobulin heavy variable 3/OR16-9 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5644]","synonyms":"IGHV3/OR16-9","biotype":"IG_V_gene","ncbi_id":"28307","summary":null,"start":32066065,"end":32066358,"strand":1,"description":"immunoglobulin heavy variable 3/OR16-9 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5644]"}, {"versioned_ensembl_gene_id":"ENSG00000231011.1","gene_symbol":"AC092832.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22616744,"end":22617143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261289.2","gene_symbol":"AC034105.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31952160,"end":31952473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233067.2","gene_symbol":"PTCHD1-AS","gene_name":"PTCHD1 antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:37703]","synonyms":"PTCHD1AS2,PTCHD1AS1,DDX53-AS1","biotype":"lincRNA","ncbi_id":"100873065","summary":null,"start":22259797,"end":23293146,"strand":-1,"description":"PTCHD1 antisense RNA (head to head) [Source:HGNC Symbol;Acc:HGNC:37703]"}, {"versioned_ensembl_gene_id":"ENSG00000281737.1","gene_symbol":"AC116165.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23145340,"end":23149199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223931.2","gene_symbol":"AC142381.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32051825,"end":32052280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261704.2","gene_symbol":"IGHV1OR16-1","gene_name":"immunoglobulin heavy variable 1/OR16-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5570]","synonyms":"IGHV1/OR16-1","biotype":"IG_V_pseudogene","ncbi_id":"28315","summary":null,"start":32034853,"end":32035326,"strand":1,"description":"immunoglobulin heavy variable 1/OR16-1 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5570]"}, {"versioned_ensembl_gene_id":"ENSG00000281670.1","gene_symbol":"CABIN1","gene_name":"calcineurin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24187]","synonyms":"PPP3IN,KIAA0330","biotype":"processed_transcript","ncbi_id":"23523","summary":"Calcineurin plays an important role in the T-cell receptor-mediated signal transduction pathway. The protein encoded by this gene binds specifically to the activated form of calcineurin and inhibits calcineurin-mediated signal transduction. The encoded protein is found in the nucleus and contains a leucine zipper domain as well as several PEST motifs, sequences which confer targeted degradation to those proteins which contain them. Alternative splicing results in multiple transcript variants encoding two different isoforms. [provided by RefSeq, Jan 2011]","start":24065455,"end":24065991,"strand":1,"description":"calcineurin binding protein 1 [Source:HGNC Symbol;Acc:HGNC:24187]"}, {"versioned_ensembl_gene_id":"ENSG00000197476.3","gene_symbol":"AC034105.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":31962063,"end":31962381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237019.1","gene_symbol":"AC004470.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22698457,"end":22768966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260048.2","gene_symbol":"IGHV1OR16-3","gene_name":"immunoglobulin heavy variable 1/OR16-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5572]","synonyms":"IGHV1/OR16-3","biotype":"IG_V_pseudogene","ncbi_id":"28313","summary":null,"start":32059084,"end":32059372,"strand":1,"description":"immunoglobulin heavy variable 1/OR16-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5572]"}, {"versioned_ensembl_gene_id":"ENSG00000184735.6","gene_symbol":"DDX53","gene_name":"DEAD-box helicase 53 [Source:HGNC Symbol;Acc:HGNC:20083]","synonyms":"CT26,CAGE","biotype":"protein_coding","ncbi_id":"168400","summary":"This intronless gene encodes a protein which contains several domains found in members of the DEAD-box helicase protein family. Other members of this protein family participate in ATP-dependent RNA unwinding. [provided by RefSeq, Sep 2011]","start":22999961,"end":23003589,"strand":1,"description":"DEAD-box helicase 53 [Source:HGNC Symbol;Acc:HGNC:20083]"}, {"versioned_ensembl_gene_id":"ENSG00000215537.3","gene_symbol":"ZNF736P11Y","gene_name":"zinc finger protein 736 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:38426]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419730","summary":null,"start":22866544,"end":22867756,"strand":-1,"description":"zinc finger protein 736 pseudogene 11, Y-linked [Source:HGNC Symbol;Acc:HGNC:38426]"}, {"versioned_ensembl_gene_id":"ENSG00000236106.1","gene_symbol":"AC010729.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":5726449,"end":5730342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226906.1","gene_symbol":"TTTY4","gene_name":"testis-specific transcript, Y-linked 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16481]","synonyms":"TTTY4A,LINC00123,TTY4","biotype":"lincRNA","ncbi_id":"114761","summary":"There are three copies of this gene on chromosome Y. This record represents the most centromeric copy. [provided by RefSeq, Jul 2008]","start":22936455,"end":22973284,"strand":1,"description":"testis-specific transcript, Y-linked 4 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:16481]"}, {"versioned_ensembl_gene_id":"ENSG00000171119.2","gene_symbol":"NRTN","gene_name":"neurturin [Source:HGNC Symbol;Acc:HGNC:8007]","synonyms":"NTN","biotype":"protein_coding","ncbi_id":"4902","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein signals through the RET receptor tyrosine kinase and a GPI-linked coreceptor, and promotes survival of neuronal populations. A neurturin mutation has been described in a family with Hirschsprung Disease. [provided by RefSeq, Aug 2016]","start":5823802,"end":5828324,"strand":1,"description":"neurturin [Source:HGNC Symbol;Acc:HGNC:8007]"}, {"versioned_ensembl_gene_id":"ENSG00000237266.1","gene_symbol":"LINC01810","gene_name":"long intergenic non-protein coding RNA 1810 [Source:HGNC Symbol;Acc:HGNC:52613]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105373400","summary":null,"start":5810641,"end":5812596,"strand":-1,"description":"long intergenic non-protein coding RNA 1810 [Source:HGNC Symbol;Acc:HGNC:52613]"}, {"versioned_ensembl_gene_id":"ENSG00000205795.4","gene_symbol":"CYS1","gene_name":"cystin 1 [Source:HGNC Symbol;Acc:HGNC:18525]","synonyms":null,"biotype":"protein_coding","ncbi_id":"192668","summary":null,"start":10056780,"end":10080944,"strand":-1,"description":"cystin 1 [Source:HGNC Symbol;Acc:HGNC:18525]"}, {"versioned_ensembl_gene_id":"ENSG00000175809.5","gene_symbol":"ZNF645","gene_name":"zinc finger protein 645 [Source:HGNC Symbol;Acc:HGNC:26371]","synonyms":"HAKAIL,FLJ25735,CT138","biotype":"protein_coding","ncbi_id":"158506","summary":"This gene encodes a member of the zinc finger domain-containing protein family. This family member contains both a RING-type and a C2H2-type of zinc finger domain, and it may function as an E3 ubiquitin-protein ligase. Protein localization suggests a role in human sperm production and quality control. [provided by RefSeq, Aug 2011]","start":22272943,"end":22274461,"strand":1,"description":"zinc finger protein 645 [Source:HGNC Symbol;Acc:HGNC:26371]"}, {"versioned_ensembl_gene_id":"ENSG00000233948.10","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RFP,RNF76","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28903164,"end":28924151,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000276983.1","gene_symbol":"AC009892.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54560000,"end":54560286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234993.1","gene_symbol":"CUBNP2","gene_name":"cubilin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44984]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100289280","summary":null,"start":45232026,"end":45247361,"strand":-1,"description":"cubilin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44984]"}, {"versioned_ensembl_gene_id":"ENSG00000239701.1","gene_symbol":"AC006512.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7032108,"end":7032398,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233222.2","gene_symbol":"AL513523.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153750983,"end":153752176,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271014.1","gene_symbol":"AC062037.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85360798,"end":85360925,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273196.1","gene_symbol":"AC062037.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85387074,"end":85387146,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243613.1","gene_symbol":"AL513523.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":153746851,"end":153751227,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000111684.10","gene_symbol":"LPCAT3","gene_name":"lysophosphatidylcholine acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30244]","synonyms":"OACT5,nessy,MBOAT5,C3F","biotype":"protein_coding","ncbi_id":"10162","summary":null,"start":6976186,"end":7018510,"strand":-1,"description":"lysophosphatidylcholine acyltransferase 3 [Source:HGNC Symbol;Acc:HGNC:30244]"}, {"versioned_ensembl_gene_id":"ENSG00000178429.9","gene_symbol":"RPS3AP5","gene_name":"ribosomal protein S3A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23744]","synonyms":"bA486O22.3","biotype":"processed_pseudogene","ncbi_id":"439992","summary":null,"start":84560443,"end":84561263,"strand":1,"description":"ribosomal protein S3A pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:23744]"}, {"versioned_ensembl_gene_id":"ENSG00000120555.13","gene_symbol":"SEPT7P9","gene_name":"septin 7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30810]","synonyms":"SEPT7L,CDC10L,bA291L22.2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"285961","summary":null,"start":38383069,"end":38402916,"strand":-1,"description":"septin 7 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:30810]"}, {"versioned_ensembl_gene_id":"ENSG00000272835.3","gene_symbol":"SMDT1","gene_name":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]","synonyms":"dJ186O1.1,DDDD,C22orf32,EMRE","biotype":"protein_coding","ncbi_id":"91689","summary":"This gene encodes a core regulatory component of a calcium channel in the mitochondrial inner membrane. [provided by RefSeq, Apr 2017]","start":42079691,"end":42084284,"strand":1,"description":"single-pass membrane protein with aspartate rich tail 1 [Source:HGNC Symbol;Acc:HGNC:25055]"}, {"versioned_ensembl_gene_id":"ENSG00000143554.13","gene_symbol":"SLC27A3","gene_name":"solute carrier family 27 member 3 [Source:HGNC Symbol;Acc:HGNC:10997]","synonyms":"FATP3,ACSVL3,MGC4365","biotype":"protein_coding","ncbi_id":"11000","summary":"This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]","start":153774354,"end":153780157,"strand":1,"description":"solute carrier family 27 member 3 [Source:HGNC Symbol;Acc:HGNC:10997]"}, {"versioned_ensembl_gene_id":"ENSG00000115459.17","gene_symbol":"ELMOD3","gene_name":"ELMO domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26158]","synonyms":"FLJ21977,DFNB88,RBM29,RBED1","biotype":"protein_coding","ncbi_id":"84173","summary":"This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]","start":85354394,"end":85391752,"strand":1,"description":"ELMO domain containing 3 [Source:HGNC Symbol;Acc:HGNC:26158]"}, {"versioned_ensembl_gene_id":"ENSG00000268062.1","gene_symbol":"AL031274.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171345105,"end":171345307,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183753.10","gene_symbol":"BPY2","gene_name":"basic charge, Y-linked, 2 [Source:HGNC Symbol;Acc:HGNC:13508]","synonyms":"VCY2A,VCY2,BPY2A","biotype":"protein_coding","ncbi_id":"9083","summary":"This gene is located in the nonrecombining portion of the Y chromosome, and expressed specifically in testis. The encoded protein interacts with ubiquitin protein ligase E3A and may be involved in male germ cell development and male infertility. Three nearly identical copies of this gene exist on chromosome Y; two copies are part of a palindromic region. This record represents the copy outside of the palidromic region. [provided by RefSeq, Jul 2008]","start":22973819,"end":23005465,"strand":1,"description":"basic charge, Y-linked, 2 [Source:HGNC Symbol;Acc:HGNC:13508]"}, {"versioned_ensembl_gene_id":"ENSG00000278996.1","gene_symbol":"FP671120.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8197620,"end":8227646,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225704.2","gene_symbol":"AL031274.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":171345089,"end":171345320,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237267.1","gene_symbol":"LINC01519","gene_name":"long intergenic non-protein coding RNA 1519 [Source:HGNC Symbol;Acc:HGNC:51217]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929624","summary":null,"start":85193421,"end":85197958,"strand":-1,"description":"long intergenic non-protein coding RNA 1519 [Source:HGNC Symbol;Acc:HGNC:51217]"}, {"versioned_ensembl_gene_id":"ENSG00000280800.1","gene_symbol":"FP671120.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8210384,"end":8211306,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183762.12","gene_symbol":"KREMEN1","gene_name":"kringle containing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:17550]","synonyms":"KRM1,KREMEN","biotype":"protein_coding","ncbi_id":"83999","summary":"This gene encodes a high-affinity dickkopf homolog 1 (DKK1) transmembrane receptor that functionally cooperates with DKK1 to block wingless (WNT)/beta-catenin signaling. The encoded protein is a component of a membrane complex that modulates canonical WNT signaling through lipoprotein receptor-related protein 6 (LRP6). It contains extracellular kringle, WSC, and CUB domains. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene. [provided by RefSeq, Jul 2008]","start":29073078,"end":29168333,"strand":1,"description":"kringle containing transmembrane protein 1 [Source:HGNC Symbol;Acc:HGNC:17550]"}, {"versioned_ensembl_gene_id":"ENSG00000225636.1","gene_symbol":"HNRNPA3P15","gene_name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:48761]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480234","summary":null,"start":197014990,"end":197016015,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:48761]"}, {"versioned_ensembl_gene_id":"ENSG00000224442.1","gene_symbol":"AC017035.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":197028711,"end":197030143,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231621.1","gene_symbol":"AC013264.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":197197991,"end":197199273,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213642.3","gene_symbol":"AC016769.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64569428,"end":64570437,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196632.10","gene_symbol":"WNK3","gene_name":"WNK lysine deficient protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:14543]","synonyms":"PRKWNK3","biotype":"protein_coding","ncbi_id":"65267","summary":"This gene encodes a protein belonging to the 'with no lysine' family of serine-threonine protein kinases. These family members lack the catalytic lysine in subdomain II, and instead have a conserved lysine in subdomain I. This family member functions as a positive regulator of the transcellular Ca2+ transport pathway, and it plays a role in the increase of cell survival in a caspase-3-dependent pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]","start":54192823,"end":54358642,"strand":-1,"description":"WNK lysine deficient protein kinase 3 [Source:HGNC Symbol;Acc:HGNC:14543]"}, {"versioned_ensembl_gene_id":"ENSG00000163131.10","gene_symbol":"CTSS","gene_name":"cathepsin S [Source:HGNC Symbol;Acc:HGNC:2545]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1520","summary":"The preproprotein encoded by this gene, a member of the peptidase C1 family, is a lysosomal cysteine proteinase that participates in the degradation of antigenic proteins to peptides for presentation on MHC class II molecules. The mature protein cleaves the invariant chain of MHC class II molecules in endolysosomal compartments and enables the formation of antigen-MHC class II complexes and the proper display of extracellular antigenic peptides by MHC-II. The mature protein also functions as an elastase over a broad pH range. When secreted from cells, this protein can remodel components of the extracellular matrix such as elastin, collagen, and fibronectin. This gene is implicated in the pathology of many inflammatory and autoimmune diseases and, given its elastase activity, plays a significant role in some pulmonary diseases. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2020]","start":150730196,"end":150765957,"strand":-1,"description":"cathepsin S [Source:HGNC Symbol;Acc:HGNC:2545]"}, {"versioned_ensembl_gene_id":"ENSG00000224669.1","gene_symbol":"AC016769.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64582733,"end":64583207,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257548.1","gene_symbol":"AC078929.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107093298,"end":107123314,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230482.1","gene_symbol":"ATP5G2P3","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42187]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100507097","summary":null,"start":197263111,"end":197263535,"strand":1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42187]"}, {"versioned_ensembl_gene_id":"ENSG00000236977.1","gene_symbol":"ANKRD44-IT1","gene_name":"ANKRD44 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41477]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"101927547","summary":null,"start":197250858,"end":197302519,"strand":-1,"description":"ANKRD44 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:41477]"}, {"versioned_ensembl_gene_id":"ENSG00000234595.1","gene_symbol":"AC013733.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181683113,"end":181685707,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278508.3","gene_symbol":"GOLGA8EP","gene_name":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]","synonyms":"GOLGA8E","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"390535","summary":null,"start":23162205,"end":23173124,"strand":1,"description":"golgin A8 family member E, pseudogene [Source:HGNC Symbol;Acc:HGNC:32377]"}, {"versioned_ensembl_gene_id":"ENSG00000233502.1","gene_symbol":"AC104794.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":10083781,"end":10086101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276475.1","gene_symbol":"AC016769.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64590599,"end":64591133,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225570.1","gene_symbol":"AC013733.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":181690380,"end":181693415,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226310.1","gene_symbol":"AL022157.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":57121662,"end":57127243,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223873.1","gene_symbol":"SAP18P2","gene_name":"SAP18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51568]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442060","summary":null,"start":181694442,"end":181694900,"strand":1,"description":"SAP18 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:51568]"}, {"versioned_ensembl_gene_id":"ENSG00000244000.1","gene_symbol":"AC006366.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23017063,"end":23017821,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000065413.18","gene_symbol":"ANKRD44","gene_name":"ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:HGNC:25259]","synonyms":"PP6-ARS-B","biotype":"protein_coding","ncbi_id":"91526","summary":null,"start":196967017,"end":197311173,"strand":-1,"description":"ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:HGNC:25259]"}, {"versioned_ensembl_gene_id":"ENSG00000155158.20","gene_symbol":"TTC39B","gene_name":"tetratricopeptide repeat domain 39B [Source:HGNC Symbol;Acc:HGNC:23704]","synonyms":"FLJ33868,C9orf52","biotype":"protein_coding","ncbi_id":"158219","summary":null,"start":15163622,"end":15307360,"strand":-1,"description":"tetratricopeptide repeat domain 39B [Source:HGNC Symbol;Acc:HGNC:23704]"}, {"versioned_ensembl_gene_id":"ENSG00000166471.10","gene_symbol":"TMEM41B","gene_name":"transmembrane protein 41B [Source:HGNC Symbol;Acc:HGNC:28948]","synonyms":"KIAA0033","biotype":"protein_coding","ncbi_id":"440026","summary":null,"start":9280654,"end":9314780,"strand":-1,"description":"transmembrane protein 41B [Source:HGNC Symbol;Acc:HGNC:28948]"}, {"versioned_ensembl_gene_id":"ENSG00000106123.11","gene_symbol":"EPHB6","gene_name":"EPH receptor B6 [Source:HGNC Symbol;Acc:HGNC:3396]","synonyms":"HEP","biotype":"protein_coding","ncbi_id":"2051","summary":"This gene encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins. Unlike other members of this family, the encoded protein does not contain a functional kinase domain. Activity of this protein can influence cell adhesion and migration. Expression of this gene is downregulated during tumor progression, suggesting that the protein may suppress tumor invasion and metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":142855061,"end":142871094,"strand":1,"description":"EPH receptor B6 [Source:HGNC Symbol;Acc:HGNC:3396]"}, {"versioned_ensembl_gene_id":"ENSG00000269427.1","gene_symbol":"AC024075.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16630743,"end":16643942,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000187045.16","gene_symbol":"TMPRSS6","gene_name":"transmembrane protease, serine 6 [Source:HGNC Symbol;Acc:HGNC:16517]","synonyms":"FLJ30744","biotype":"protein_coding","ncbi_id":"164656","summary":"The protein encoded by this gene is a type II transmembrane serine proteinase that is found attached to the cell surface. The encoded protein may be involved in matrix remodeling processes in the liver. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]","start":37065436,"end":37109563,"strand":-1,"description":"transmembrane protease, serine 6 [Source:HGNC Symbol;Acc:HGNC:16517]"}, {"versioned_ensembl_gene_id":"ENSG00000269044.2","gene_symbol":"AC024075.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16633797,"end":16635269,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232044.6","gene_symbol":"LINC01105","gene_name":"long intergenic non-protein coding RNA 1105 [Source:HGNC Symbol;Acc:HGNC:26403]","synonyms":"LOC150622,FLJ30594","biotype":"processed_transcript","ncbi_id":"150622","summary":null,"start":5932687,"end":6001275,"strand":1,"description":"long intergenic non-protein coding RNA 1105 [Source:HGNC Symbol;Acc:HGNC:26403]"}, {"versioned_ensembl_gene_id":"ENSG00000267904.1","gene_symbol":"AC024075.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16639967,"end":16640668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269578.1","gene_symbol":"AC008764.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":16586905,"end":16587985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234566.1","gene_symbol":"RPL7AP71","gene_name":"ribosomal protein L7a pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:35754]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271399","summary":null,"start":54223324,"end":54224062,"strand":1,"description":"ribosomal protein L7a pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:35754]"}, {"versioned_ensembl_gene_id":"ENSG00000127526.14","gene_symbol":"SLC35E1","gene_name":"solute carrier family 35 member E1 [Source:HGNC Symbol;Acc:HGNC:20803]","synonyms":"FLJ14251","biotype":"protein_coding","ncbi_id":"79939","summary":null,"start":16549831,"end":16572382,"strand":-1,"description":"solute carrier family 35 member E1 [Source:HGNC Symbol;Acc:HGNC:20803]"}, {"versioned_ensembl_gene_id":"ENSG00000147804.9","gene_symbol":"SLC39A4","gene_name":"solute carrier family 39 member 4 [Source:HGNC Symbol;Acc:HGNC:17129]","synonyms":"ZIP4,AWMS2,AEZ","biotype":"protein_coding","ncbi_id":"55630","summary":"This gene encodes a member of the zinc/iron-regulated transporter-like protein (ZIP) family. The encoded protein localizes to cell membranes and is required for zinc uptake in the intestine. Mutations in this gene result in acrodermatitis enteropathica. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]","start":144409742,"end":144416895,"strand":-1,"description":"solute carrier family 39 member 4 [Source:HGNC Symbol;Acc:HGNC:17129]"}, {"versioned_ensembl_gene_id":"ENSG00000134575.9","gene_symbol":"ACP2","gene_name":"acid phosphatase 2, lysosomal [Source:HGNC Symbol;Acc:HGNC:123]","synonyms":"LAP","biotype":"protein_coding","ncbi_id":"53","summary":"The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017]","start":47239302,"end":47248906,"strand":-1,"description":"acid phosphatase 2, lysosomal [Source:HGNC Symbol;Acc:HGNC:123]"}, {"versioned_ensembl_gene_id":"ENSG00000262296.1","gene_symbol":"AC118755.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9647020,"end":9647660,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106009.15","gene_symbol":"BRAT1","gene_name":"BRCA1 associated ATM activator 1 [Source:HGNC Symbol;Acc:HGNC:21701]","synonyms":"MGC22916,C7orf27,BAAT1","biotype":"protein_coding","ncbi_id":"221927","summary":"The protein encoded by this ubiquitously expressed gene interacts with the tumor suppressing BRCA1 (breast cancer 1) protein and and the ATM (ataxia telangiectasia mutated) protein. ATM is thought to be a master controller of cell cycle checkpoint signalling pathways that are required for cellular responses to DNA damage such as double-strand breaks that are induced by ionizing radiation and complexes with BRCA1 in the multi-protein complex BASC (BRAC1-associated genome surveillance complex). The protein encoded by this gene is thought to play a role in the DNA damage pathway regulated by BRCA1 and ATM. [provided by RefSeq, Mar 2012]","start":2537877,"end":2555727,"strand":-1,"description":"BRCA1 associated ATM activator 1 [Source:HGNC Symbol;Acc:HGNC:21701]"}, {"versioned_ensembl_gene_id":"ENSG00000226772.1","gene_symbol":"AL021393.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29099041,"end":29111683,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277131.4","gene_symbol":"MMEL1","gene_name":"membrane metalloendopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:14668]","synonyms":"SEP,NL2,NL1,NEPII,MMEL2","biotype":"protein_coding","ncbi_id":"79258","summary":"The protein encoded by this gene is a member of the neutral endopeptidase (NEP) or membrane metallo-endopeptidase (MME) family. Family members play important roles in pain perception, arterial pressure regulation, phosphate metabolism and homeostasis. This protein is a type II transmembrane protein and is thought to be expressed as a secreted protein. This gene is expressed mainly in testis with weak expression in the brain, kidney, and heart. [provided by RefSeq, Jul 2008]","start":2590639,"end":2632987,"strand":-1,"description":"membrane metalloendopeptidase like 1 [Source:HGNC Symbol;Acc:HGNC:14668]"}, {"versioned_ensembl_gene_id":"ENSG00000281300.1","gene_symbol":"NXN","gene_name":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]","synonyms":"NRX,FLJ12614","biotype":"protein_coding","ncbi_id":"64359","summary":"This gene encodes a member of the thioredoxin superfamily, a group of small, multifunctional redox-active proteins. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. The encoded protein acts a redox-dependent regulator of the Wnt signaling pathway and is involved in cell growth and differentiation. [provided by RefSeq, Sep 2015]","start":978299,"end":979770,"strand":-1,"description":"nucleoredoxin [Source:HGNC Symbol;Acc:HGNC:18008]"}, {"versioned_ensembl_gene_id":"ENSG00000236540.7","gene_symbol":"AC006547.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20058030,"end":20070569,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000135912.10","gene_symbol":"TTLL4","gene_name":"tubulin tyrosine ligase like 4 [Source:HGNC Symbol;Acc:HGNC:28976]","synonyms":"KIAA0173","biotype":"protein_coding","ncbi_id":"9654","summary":null,"start":218710845,"end":218755416,"strand":1,"description":"tubulin tyrosine ligase like 4 [Source:HGNC Symbol;Acc:HGNC:28976]"}, {"versioned_ensembl_gene_id":"ENSG00000120697.8","gene_symbol":"ALG5","gene_name":"ALG5, dolichyl-phosphate beta-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:20266]","synonyms":"bA421P11.2","biotype":"protein_coding","ncbi_id":"29880","summary":"This gene encodes a member of the glycosyltransferase 2 family. The encoded protein participates in glucosylation of the oligomannose core in N-linked glycosylation of proteins. The addition of glucose residues to the oligomannose core is necessary to ensure substrate recognition, and therefore, effectual transfer of the oligomannose core to the nascent glycoproteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]","start":36949775,"end":37000261,"strand":-1,"description":"ALG5, dolichyl-phosphate beta-glucosyltransferase [Source:HGNC Symbol;Acc:HGNC:20266]"}, {"versioned_ensembl_gene_id":"ENSG00000183597.15","gene_symbol":"TANGO2","gene_name":"transport and golgi organization 2 homolog [Source:HGNC Symbol;Acc:HGNC:25439]","synonyms":"DKFZp761P1121,C22orf25","biotype":"protein_coding","ncbi_id":"128989","summary":"This gene belongs to the transport and Golgi organization family, whose members are predicted to play roles in secretory protein loading in the endoplasmic reticulum. Depletion of this gene in Drosophila S2 cells causes fusion of the Golgi with the ER. In mouse tissue culture cells, this protein co-localizes with a mitochondrially targeted mCherry protein and displays very low levels of co-localization with Golgi and peroxisomes. Allelic variants of this gene are associated with rhabdomyolysis, metabolic crises with encephalopathy, and cardiac arrhythmia. [provided by RefSeq, Apr 2016]","start":20017014,"end":20065926,"strand":1,"description":"transport and golgi organization 2 homolog [Source:HGNC Symbol;Acc:HGNC:25439]"}, {"versioned_ensembl_gene_id":"ENSG00000233783.7","gene_symbol":"AP001442.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":25928754,"end":25942686,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273492.5","gene_symbol":"AP000229.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":26170871,"end":26217381,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231366.1","gene_symbol":"RPS26P40","gene_name":"ribosomal protein S26 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36906]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"338611","summary":null,"start":70794230,"end":70794523,"strand":-1,"description":"ribosomal protein S26 pseudogene 40 [Source:HGNC Symbol;Acc:HGNC:36906]"}, {"versioned_ensembl_gene_id":"ENSG00000187871.2","gene_symbol":"GFRAL","gene_name":"GDNF family receptor alpha like [Source:HGNC Symbol;Acc:HGNC:32789]","synonyms":"UNQ9356,GRAL,C6orf144,bA360D14.1","biotype":"protein_coding","ncbi_id":"389400","summary":null,"start":55327469,"end":55402493,"strand":1,"description":"GDNF family receptor alpha like [Source:HGNC Symbol;Acc:HGNC:32789]"}, {"versioned_ensembl_gene_id":"ENSG00000270192.1","gene_symbol":"MRPS35P3","gene_name":"mitochondrial ribosomal protein S35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29770]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"359779","summary":null,"start":57982285,"end":57982993,"strand":1,"description":"mitochondrial ribosomal protein S35 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:29770]"}, {"versioned_ensembl_gene_id":"ENSG00000156413.13","gene_symbol":"FUT6","gene_name":"fucosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:4017]","synonyms":"FucT-VI,FT1A,FLJ40754,FCT3A","biotype":"protein_coding","ncbi_id":"2528","summary":"The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of sialyl-Lewis X, an E-selectin ligand. Mutations in this gene are a cause of fucosyltransferase-6 deficiency. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":5830610,"end":5839731,"strand":-1,"description":"fucosyltransferase 6 [Source:HGNC Symbol;Acc:HGNC:4017]"}, {"versioned_ensembl_gene_id":"ENSG00000232115.1","gene_symbol":"AC026884.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58106423,"end":58106879,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181798.2","gene_symbol":"LINC00471","gene_name":"long intergenic non-protein coding RNA 471 [Source:HGNC Symbol;Acc:HGNC:28668]","synonyms":"MGC43122,C2orf52","biotype":"lincRNA","ncbi_id":"151477","summary":null,"start":231508426,"end":231514339,"strand":-1,"description":"long intergenic non-protein coding RNA 471 [Source:HGNC Symbol;Acc:HGNC:28668]"}, {"versioned_ensembl_gene_id":"ENSG00000180221.6","gene_symbol":"TPT1P10","gene_name":"tumor protein, translationally-controlled 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101928715","summary":null,"start":58212541,"end":58213036,"strand":-1,"description":"tumor protein, translationally-controlled 1 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:49301]"}, {"versioned_ensembl_gene_id":"ENSG00000085872.14","gene_symbol":"CHERP","gene_name":"calcium homeostasis endoplasmic reticulum protein [Source:HGNC Symbol;Acc:HGNC:16930]","synonyms":"ERPROT213-21,DAN16","biotype":"protein_coding","ncbi_id":"10523","summary":null,"start":16517889,"end":16542530,"strand":-1,"description":"calcium homeostasis endoplasmic reticulum protein [Source:HGNC Symbol;Acc:HGNC:16930]"}, {"versioned_ensembl_gene_id":"ENSG00000271989.1","gene_symbol":"AL139424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":10429881,"end":10430677,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151151.5","gene_symbol":"IPMK","gene_name":"inositol polyphosphate multikinase [Source:HGNC Symbol;Acc:HGNC:20739]","synonyms":null,"biotype":"protein_coding","ncbi_id":"253430","summary":"This gene encodes a member of the inositol phosphokinase family. The encoded protein has 3-kinase, 5-kinase and 6-kinase activities on phosphorylated inositol substrates. The encoded protein plays an important role in the biosynthesis of inositol 1,3,4,5,6-pentakisphosphate, and has a preferred 5-kinase activity. This gene may play a role in nuclear mRNA export. Pseudogenes of this gene are located on the long arm of chromosome 13 and the short arm of chromosome 19. [provided by RefSeq, Dec 2010]","start":58191517,"end":58267934,"strand":-1,"description":"inositol polyphosphate multikinase [Source:HGNC Symbol;Acc:HGNC:20739]"}, {"versioned_ensembl_gene_id":"ENSG00000162545.5","gene_symbol":"CAMK2N1","gene_name":"calcium/calmodulin dependent protein kinase II inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:24190]","synonyms":"CaMKIINalpha","biotype":"protein_coding","ncbi_id":"55450","summary":null,"start":20482391,"end":20486220,"strand":-1,"description":"calcium/calmodulin dependent protein kinase II inhibitor 1 [Source:HGNC Symbol;Acc:HGNC:24190]"}, {"versioned_ensembl_gene_id":"ENSG00000251503.8","gene_symbol":"CENPS-CORT","gene_name":"CENPS-CORT readthrough [Source:HGNC Symbol;Acc:HGNC:38843]","synonyms":"APITD1-CORT","biotype":"protein_coding","ncbi_id":"100526739","summary":"This locus represents naturally occurring read-through transcription between the neighboring APITD1 (apoptosis-inducing, TAF9-like domain 1) and CORT (cortistatin) genes. Alternative splicing results in multiple transcript variants, two of which encode fusion proteins that share sequence identity with the products of each individual gene. [provided by RefSeq, Aug 2011]","start":10430102,"end":10452153,"strand":1,"description":"CENPS-CORT readthrough [Source:HGNC Symbol;Acc:HGNC:38843]"}, {"versioned_ensembl_gene_id":"ENSG00000187624.8","gene_symbol":"C17orf97","gene_name":"chromosome 17 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:33800]","synonyms":"LOC400566,LIAT1","biotype":"protein_coding","ncbi_id":"400566","summary":null,"start":410327,"end":431062,"strand":1,"description":"chromosome 17 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:33800]"}, {"versioned_ensembl_gene_id":"ENSG00000254884.1","gene_symbol":"PRR13P2","gene_name":"proline rich 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50615]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480303","summary":null,"start":9311284,"end":9311689,"strand":-1,"description":"proline rich 13 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:50615]"}, {"versioned_ensembl_gene_id":"ENSG00000260742.1","gene_symbol":"AC009962.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":181887851,"end":181891663,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280821.1","gene_symbol":"AC236040.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42148576,"end":42150238,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280750.1","gene_symbol":"AL021878.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42089630,"end":42090028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281417.1","gene_symbol":"AC236040.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42132528,"end":42132983,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000272532.6","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CYP2D8P2,CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP,CPD6,P450C2D","biotype":"polymorphic_pseudogene","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126481,"end":42130888,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000241525.4","gene_symbol":"AC141424.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":404468,"end":414023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276016.4","gene_symbol":"ABR","gene_name":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]","synonyms":"MDB","biotype":"protein_coding","ncbi_id":"29","summary":"This gene encodes a protein that is similar to the protein encoded by the breakpoint cluster region gene located on chromosome 22. The protein encoded by this gene contains a GTPase-activating protein domain, a domain found in members of the Rho family of GTP-binding proteins. Functional studies in mice determined that this protein plays a role in vestibular morphogenesis. Alternatively spliced transcript variants have been reported for this gene. [provided by RefSeq, Feb 2012]","start":1003519,"end":1116206,"strand":-1,"description":"active BCR-related [Source:HGNC Symbol;Acc:HGNC:81]"}, {"versioned_ensembl_gene_id":"ENSG00000244265.1","gene_symbol":"SIAH2-AS1","gene_name":"SIAH2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40526]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874005","summary":null,"start":150761937,"end":150762538,"strand":1,"description":"SIAH2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40526]"}, {"versioned_ensembl_gene_id":"ENSG00000276805.2","gene_symbol":"AL133216.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":38403189,"end":38452153,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000181788.3","gene_symbol":"SIAH2","gene_name":"siah E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:10858]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6478","summary":"This gene encodes a protein that is a member of the seven in absentia homolog (SIAH) family. The protein is an E3 ligase and is involved in ubiquitination and proteasome-mediated degradation of specific proteins. The activity of this ubiquitin ligase has been implicated in regulating cellular response to hypoxia. [provided by RefSeq, Jul 2008]","start":150741127,"end":150763477,"strand":-1,"description":"siah E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:10858]"}, {"versioned_ensembl_gene_id":"ENSG00000120699.12","gene_symbol":"EXOSC8","gene_name":"exosome component 8 [Source:HGNC Symbol;Acc:HGNC:17035]","synonyms":"EAP2,CIP3,bA421P11.3,Rrp43p,RRP43,p9,OIP2","biotype":"protein_coding","ncbi_id":"11340","summary":"This gene encodes a 3'-5' exoribonuclease that specifically interacts with mRNAs containing AU-rich elements. The encoded protein is part of the exosome complex that is important for the degradation of numerous RNA species. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Mar 2009]","start":36998816,"end":37009613,"strand":1,"description":"exosome component 8 [Source:HGNC Symbol;Acc:HGNC:17035]"}, {"versioned_ensembl_gene_id":"ENSG00000241563.3","gene_symbol":"CORT","gene_name":"cortistatin [Source:HGNC Symbol;Acc:HGNC:2257]","synonyms":"MGC32686","biotype":"protein_coding","ncbi_id":"1325","summary":"This gene encodes a neuropeptide that is structurally similar to somatostatin. It binds to all known somatostatin receptors, and shares many pharmacological and functional properties with somatostatin, including the depression of neuronal activity. However, it also has many properties distinct from somatostatin, such as induction of slow-wave sleep, apparently by antagonism of the excitatory effects of acetylcholine on the cortex, reduction of locomotor activity, and activation of cation selective currents not responsive to somatostatin. The preproprotein undergoes further processing into multiple mature products. Read-through transcripts exist between this gene and the upstream APITD1 (apoptosis-inducing, TAF9-like domain 1) gene, as represented in GeneID:100526739. [provided by RefSeq, Nov 2010]","start":10449719,"end":10451902,"strand":1,"description":"cortistatin [Source:HGNC Symbol;Acc:HGNC:2257]"}, {"versioned_ensembl_gene_id":"ENSG00000175279.21","gene_symbol":"CENPS","gene_name":"centromere protein S [Source:HGNC Symbol;Acc:HGNC:23163]","synonyms":"MHF1,FAAP16,CENP-S,APITD1","biotype":"protein_coding","ncbi_id":"378708","summary":"This gene was identified in the neuroblastoma tumor suppressor candidate region on chromosome 1p36. It contains a TFIID-31 domain, similar to that found in TATA box-binding protein-associated factor, TAF(II)31, which is required for p53-mediated transcription activation. This gene was expressed at very low levels in neuroblastoma tumors, and was shown to reduce cell growth in neuroblastoma cells, suggesting that it may have a role in a cell death pathway. The protein is a component of multiple complexes, including the Fanconi anemia (FA) core complex, the APITD1/CENPS complex, and the CENPA-CAD (nucleosome distal) complex. Known functions include an involvement with chromatin associations of the FA core complex, and a role in the stable assembly of the outer kinetochore. Alternative splicing of this gene results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream cortistatin (CORT) gene, as represented in GeneID:100526739. An APITD1-related pseudogene has been identified on chromosome 7. [provided by RefSeq, Nov 2010]","start":10430443,"end":10442809,"strand":1,"description":"centromere protein S [Source:HGNC Symbol;Acc:HGNC:23163]"}, {"versioned_ensembl_gene_id":"ENSG00000241654.1","gene_symbol":"AC087501.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9589902,"end":9590482,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229851.1","gene_symbol":"ARSD-AS1","gene_name":"ARSD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40085]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506356","summary":null,"start":2904904,"end":2906081,"strand":1,"description":"ARSD antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40085]"}, {"versioned_ensembl_gene_id":"ENSG00000196834.11","gene_symbol":"POTEI","gene_name":"POTE ankyrin domain family member I [Source:HGNC Symbol;Acc:HGNC:37093]","synonyms":"POTE2beta","biotype":"protein_coding","ncbi_id":"653269","summary":null,"start":130459455,"end":130509666,"strand":-1,"description":"POTE ankyrin domain family member I [Source:HGNC Symbol;Acc:HGNC:37093]"}, {"versioned_ensembl_gene_id":"ENSG00000268439.5","gene_symbol":"EMG1","gene_name":"EMG1, N1-specific pseudouridine methyltransferase [Source:HGNC Symbol;Acc:HGNC:16912]","synonyms":"Grcc2f,C2F,NEP1,Grcc2f,C2F,NEP1","biotype":"protein_coding","ncbi_id":"10436","summary":"This gene encodes an essential, conserved eukaryotic protein that methylates pseudouridine in 18S rRNA. The related protein in yeast is a component of the small subunit processome and is essential for biogenesis of the ribosomal 40S subunit. A mutation in this gene has been associated with Bowen-Conradi syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":6970921,"end":6997428,"strand":1,"description":"EMG1, N1-specific pseudouridine methyltransferase [Source:HGNC Symbol;Acc:HGNC:16912]"}, {"versioned_ensembl_gene_id":"ENSG00000154914.16","gene_symbol":"USP43","gene_name":"ubiquitin specific peptidase 43 [Source:HGNC Symbol;Acc:HGNC:20072]","synonyms":"FLJ30626","biotype":"protein_coding","ncbi_id":"124739","summary":null,"start":9644698,"end":9729691,"strand":1,"description":"ubiquitin specific peptidase 43 [Source:HGNC Symbol;Acc:HGNC:20072]"}, {"versioned_ensembl_gene_id":"ENSG00000261053.1","gene_symbol":"NAMPTP3","gene_name":"nicotinamide phosphoribosyltransferase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51313]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480319","summary":null,"start":35085896,"end":35086119,"strand":1,"description":"nicotinamide phosphoribosyltransferase pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:51313]"}, {"versioned_ensembl_gene_id":"ENSG00000150625.16","gene_symbol":"GPM6A","gene_name":"glycoprotein M6A [Source:HGNC Symbol;Acc:HGNC:4460]","synonyms":"GPM6","biotype":"protein_coding","ncbi_id":"2823","summary":null,"start":175632934,"end":176002664,"strand":-1,"description":"glycoprotein M6A [Source:HGNC Symbol;Acc:HGNC:4460]"}, {"versioned_ensembl_gene_id":"ENSG00000224402.2","gene_symbol":"OR6D1P","gene_name":"olfactory receptor family 6 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14849]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"220974","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":45255640,"end":45263252,"strand":1,"description":"olfactory receptor family 6 subfamily D member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:14849]"}, {"versioned_ensembl_gene_id":"ENSG00000090238.11","gene_symbol":"YPEL3","gene_name":"yippee like 3 [Source:HGNC Symbol;Acc:HGNC:18327]","synonyms":"MGC10500","biotype":"protein_coding","ncbi_id":"83719","summary":null,"start":30092314,"end":30096915,"strand":-1,"description":"yippee like 3 [Source:HGNC Symbol;Acc:HGNC:18327]"}, {"versioned_ensembl_gene_id":"ENSG00000253204.1","gene_symbol":"AC090281.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30921060,"end":30921335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102057.9","gene_symbol":"KCND1","gene_name":"potassium voltage-gated channel subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:6237]","synonyms":"Kv4.1","biotype":"protein_coding","ncbi_id":"3750","summary":"This gene encodes a multipass membrane protein that comprises the pore subunit of the voltage-gated A-type potassium channel, which functions in the repolarization of membrane action potentials. Activity of voltage-gated potassium channels is important in a number of physiological processes, among them the regulation of neurotransmitter release, heart rate, insulin secretion, and smooth muscle contraction. [provided by RefSeq, Aug 2013]","start":48961378,"end":48971569,"strand":-1,"description":"potassium voltage-gated channel subfamily D member 1 [Source:HGNC Symbol;Acc:HGNC:6237]"}, {"versioned_ensembl_gene_id":"ENSG00000231310.3","gene_symbol":"TBL1XR1-AS1","gene_name":"TBL1XR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41243]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874217","summary":null,"start":177037405,"end":177047923,"strand":1,"description":"TBL1XR1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41243]"}, {"versioned_ensembl_gene_id":"ENSG00000225989.9","gene_symbol":"ABCF1","gene_name":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]","synonyms":"ABC50,EST123147","biotype":"protein_coding","ncbi_id":"23","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the GCN20 subfamily. Unlike other members of the superfamily, this protein lacks the transmembrane domains which are characteristic of most ABC transporters. This protein may be regulated by tumor necrosis factor-alpha and play a role in enhancement of protein synthesis and the inflammation process. [provided by RefSeq, Jul 2008]","start":30563598,"end":30589402,"strand":1,"description":"ATP binding cassette subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:70]"}, {"versioned_ensembl_gene_id":"ENSG00000183337.16","gene_symbol":"BCOR","gene_name":"BCL6 corepressor [Source:HGNC Symbol;Acc:HGNC:20893]","synonyms":"FLJ20285,KIAA1575","biotype":"protein_coding","ncbi_id":"54880","summary":"The protein encoded by this gene was identified as an interacting corepressor of BCL6, a POZ/zinc finger transcription repressor that is required for germinal center formation and may influence apoptosis. This protein selectively interacts with the POZ domain of BCL6, but not with eight other POZ proteins. Specific class I and II histone deacetylases (HDACs) have been shown to interact with this protein, which suggests a possible link between the two classes of HDACs. Several transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome Y.[provided by RefSeq, Jun 2010]","start":40049815,"end":40177329,"strand":-1,"description":"BCL6 corepressor [Source:HGNC Symbol;Acc:HGNC:20893]"}, {"versioned_ensembl_gene_id":"ENSG00000177565.16","gene_symbol":"TBL1XR1","gene_name":"transducin beta like 1 X-linked receptor 1 [Source:HGNC Symbol;Acc:HGNC:29529]","synonyms":"TBLR1,IRA1,FLJ12894,DC42,C21","biotype":"protein_coding","ncbi_id":"79718","summary":"This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]","start":177019340,"end":177228000,"strand":-1,"description":"transducin beta like 1 X-linked receptor 1 [Source:HGNC Symbol;Acc:HGNC:29529]"}, {"versioned_ensembl_gene_id":"ENSG00000272115.1","gene_symbol":"AC233992.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":144409492,"end":144409976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226487.1","gene_symbol":"AL139254.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20412304,"end":20413253,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236963.6","gene_symbol":"LINC01141","gene_name":"long intergenic non-protein coding RNA 1141 [Source:HGNC Symbol;Acc:HGNC:49455]","synonyms":null,"biotype":"lincRNA","ncbi_id":"339505","summary":null,"start":20360579,"end":20431234,"strand":-1,"description":"long intergenic non-protein coding RNA 1141 [Source:HGNC Symbol;Acc:HGNC:49455]"}, {"versioned_ensembl_gene_id":"ENSG00000125868.15","gene_symbol":"DSTN","gene_name":"destrin, actin depolymerizing factor [Source:HGNC Symbol;Acc:HGNC:15750]","synonyms":"ADF,ACTDP","biotype":"protein_coding","ncbi_id":"11034","summary":"The product of this gene belongs to the actin-binding proteins ADF family. This family of proteins is responsible for enhancing the turnover rate of actin in vivo. This gene encodes the actin depolymerizing protein that severs actin filaments (F-actin) and binds to actin monomers (G-actin). Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":17569863,"end":17609919,"strand":1,"description":"destrin, actin depolymerizing factor [Source:HGNC Symbol;Acc:HGNC:15750]"}, {"versioned_ensembl_gene_id":"ENSG00000104472.9","gene_symbol":"CHRAC1","gene_name":"chromatin accessibility complex 1 [Source:HGNC Symbol;Acc:HGNC:13544]","synonyms":"YCL1,CHRAC15","biotype":"protein_coding","ncbi_id":"54108","summary":"CHRAC1 is a histone-fold protein that interacts with other histone-fold proteins to bind DNA in a sequence-independent manner. These histone-fold protein dimers combine within larger enzymatic complexes for DNA transcription, replication, and packaging.[supplied by OMIM, Apr 2004]","start":140511298,"end":140517137,"strand":1,"description":"chromatin accessibility complex 1 [Source:HGNC Symbol;Acc:HGNC:13544]"}, {"versioned_ensembl_gene_id":"ENSG00000122986.13","gene_symbol":"HVCN1","gene_name":"hydrogen voltage gated channel 1 [Source:HGNC Symbol;Acc:HGNC:28240]","synonyms":"VSOP,MGC15619,Hv1","biotype":"protein_coding","ncbi_id":"84329","summary":"This gene encodes a voltage-gated protein channel protein expressed more highly in certain cells of the immune system. Phagocytic cells produce superoxide anions which require this channel protein, and in B cells this same process facilitates antibody production. This same channel protein, however, can also regulate functions in other cells including spermatozoa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":110627841,"end":110704950,"strand":-1,"description":"hydrogen voltage gated channel 1 [Source:HGNC Symbol;Acc:HGNC:28240]"}, {"versioned_ensembl_gene_id":"ENSG00000273194.3","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107765,"end":42108953,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000273397.4","gene_symbol":"NDUFA6","gene_name":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]","synonyms":"LYRM6,CI-B14,B14,NADHB14","biotype":"protein_coding","ncbi_id":"4700","summary":"This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016]","start":42085525,"end":42090955,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]"}, {"versioned_ensembl_gene_id":"ENSG00000074964.16","gene_symbol":"ARHGEF10L","gene_name":"Rho guanine nucleotide exchange factor 10 like [Source:HGNC Symbol;Acc:HGNC:25540]","synonyms":"KIAA1626,FLJ10521","biotype":"protein_coding","ncbi_id":"55160","summary":"This gene belongs to the RhoGEF subfamily of RhoGTPases. Members of this subfamily are activated by specific guanine nucleotide exchange factors (GEFs) and are involved in signal transduction. The encoded protein shows cytosolic distribution. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2016]","start":17539835,"end":17697874,"strand":1,"description":"Rho guanine nucleotide exchange factor 10 like [Source:HGNC Symbol;Acc:HGNC:25540]"}, {"versioned_ensembl_gene_id":"ENSG00000227040.4","gene_symbol":"AC022483.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56760919,"end":56761485,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230655.3","gene_symbol":"AC139453.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75370448,"end":75371342,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278332.1","gene_symbol":"AL021918.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27510501,"end":27510694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230123.1","gene_symbol":"DLEC1P1","gene_name":"deleted in lung and esophageal cancer 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44545]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421153","summary":null,"start":38325237,"end":38329070,"strand":-1,"description":"deleted in lung and esophageal cancer 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44545]"}, {"versioned_ensembl_gene_id":"ENSG00000244699.1","gene_symbol":"AC139453.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":75384059,"end":75391810,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270666.1","gene_symbol":"AL021918.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27515039,"end":27515274,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000169509.5","gene_symbol":"CRCT1","gene_name":"cysteine rich C-terminal 1 [Source:HGNC Symbol;Acc:HGNC:29875]","synonyms":"NICE-1,C1orf42","biotype":"protein_coding","ncbi_id":"54544","summary":null,"start":152514502,"end":152516010,"strand":1,"description":"cysteine rich C-terminal 1 [Source:HGNC Symbol;Acc:HGNC:29875]"}, {"versioned_ensembl_gene_id":"ENSG00000105793.15","gene_symbol":"GTPBP10","gene_name":"GTP binding protein 10 [Source:HGNC Symbol;Acc:HGNC:25106]","synonyms":"OBGH2,FLJ38242,DKFZP686A10121","biotype":"protein_coding","ncbi_id":"85865","summary":"Small G proteins, such as GTPBP10, act as molecular switches that play crucial roles in the regulation of fundamental cellular processes such as protein synthesis, nuclear transport, membrane trafficking, and signal transduction (Hirano et al., 2006 [PubMed 17054726]).[supplied by OMIM, Mar 2008]","start":90335223,"end":90391455,"strand":1,"description":"GTP binding protein 10 [Source:HGNC Symbol;Acc:HGNC:25106]"}, {"versioned_ensembl_gene_id":"ENSG00000263033.2","gene_symbol":"AC007220.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":11196177,"end":11224969,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240665.1","gene_symbol":"LSP1P2","gene_name":"lymphocyte-specific protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39717]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873967","summary":null,"start":75395188,"end":75395320,"strand":1,"description":"lymphocyte-specific protein 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39717]"}, {"versioned_ensembl_gene_id":"ENSG00000218347.2","gene_symbol":"HNRNPA1P1","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13957]","synonyms":"HNRPA1P1,hnRNPA1-Lp,b34I8.2","biotype":"processed_pseudogene","ncbi_id":"645950","summary":null,"start":27523076,"end":27524339,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13957]"}, {"versioned_ensembl_gene_id":"ENSG00000242527.1","gene_symbol":"AC100771.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27483850,"end":27484128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185966.3","gene_symbol":"LCE3E","gene_name":"late cornified envelope 3E [Source:HGNC Symbol;Acc:HGNC:29463]","synonyms":"LEP17","biotype":"protein_coding","ncbi_id":"353145","summary":null,"start":152565654,"end":152566772,"strand":-1,"description":"late cornified envelope 3E [Source:HGNC Symbol;Acc:HGNC:29463]"}, {"versioned_ensembl_gene_id":"ENSG00000280613.2","gene_symbol":"NDUFA6-AS1","gene_name":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"100132273","summary":null,"start":42090931,"end":42148836,"strand":1,"description":"NDUFA6 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:45273]"}, {"versioned_ensembl_gene_id":"ENSG00000128335.13","gene_symbol":"APOL2","gene_name":"apolipoprotein L2 [Source:HGNC Symbol;Acc:HGNC:619]","synonyms":"APOL-II","biotype":"protein_coding","ncbi_id":"23780","summary":"This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":36226203,"end":36239954,"strand":-1,"description":"apolipoprotein L2 [Source:HGNC Symbol;Acc:HGNC:619]"}, {"versioned_ensembl_gene_id":"ENSG00000230495.1","gene_symbol":"AL132765.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":17599255,"end":17599807,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000128040.10","gene_symbol":"SPINK2","gene_name":"serine peptidase inhibitor, Kazal type 2 [Source:HGNC Symbol;Acc:HGNC:11245]","synonyms":"HUSI-II","biotype":"protein_coding","ncbi_id":"6691","summary":"This gene encodes a member of the family of serine protease inhibitors of the Kazal type (SPINK). The encoded protein acts as a trypsin and acrosin inhibitor in the genital tract and is localized in the spermatozoa. The protein has been associated with the progression of lymphomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]","start":56809860,"end":56821742,"strand":-1,"description":"serine peptidase inhibitor, Kazal type 2 [Source:HGNC Symbol;Acc:HGNC:11245]"}, {"versioned_ensembl_gene_id":"ENSG00000133422.12","gene_symbol":"MORC2","gene_name":"MORC family CW-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23573]","synonyms":"ZCWCC1,ZCW3,KIAA0852,AC004542.C22.1","biotype":"protein_coding","ncbi_id":"22880","summary":"This gene encodes a member of the Microrchidia (MORC) protein superfamily. The encoded protein is known to regulate the condensation of heterochromatin in response to DNA damage and play a role in repressing transcription. The protein has been found to regulate the activity of ATP citrate lyase via specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also plays a role in lipogenesis and adipocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]","start":30925130,"end":30968298,"strand":-1,"description":"MORC family CW-type zinc finger 2 [Source:HGNC Symbol;Acc:HGNC:23573]"}, {"versioned_ensembl_gene_id":"ENSG00000148943.11","gene_symbol":"LIN7C","gene_name":"lin-7 homolog C, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17789]","synonyms":"VELI3,MALS-3,Lin7c,LIN-7C,LIN-7-C,FLJ11215","biotype":"protein_coding","ncbi_id":"55327","summary":null,"start":27494576,"end":27506773,"strand":-1,"description":"lin-7 homolog C, crumbs cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:17789]"}, {"versioned_ensembl_gene_id":"ENSG00000166596.14","gene_symbol":"CFAP52","gene_name":"cilia and flagella associated protein 52 [Source:HGNC Symbol;Acc:HGNC:16053]","synonyms":"WDRPUH,WDR16,FLJ37528","biotype":"protein_coding","ncbi_id":"146845","summary":"WD repeat-containing proteins, such as WDR16, play crucial roles in a wide range of physiologic functions, including signal transduction, RNA processing, remodeling the cytoskeleton, regulation of vesicular traffic, and cell division (Silva et al., 2005 [PubMed 15967112]).[supplied by OMIM, Mar 2008]","start":9576627,"end":9643459,"strand":1,"description":"cilia and flagella associated protein 52 [Source:HGNC Symbol;Acc:HGNC:16053]"}, {"versioned_ensembl_gene_id":"ENSG00000173226.16","gene_symbol":"IQCB1","gene_name":"IQ motif containing B1 [Source:HGNC Symbol;Acc:HGNC:28949]","synonyms":"SLSN5,NPHP5,KIAA0036","biotype":"protein_coding","ncbi_id":"9657","summary":"This gene encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. The encoded protein has a central coiled-coil region and two calmodulin-binding IQ domains. It is localized to the primary cilia of renal epithelial cells and connecting cilia of photoreceptor cells. The protein is thought to play a role in ciliary function. Defects in this gene result in Senior-Loken syndrome type 5. Alternative splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Jan 2016]","start":121769763,"end":121835079,"strand":-1,"description":"IQ motif containing B1 [Source:HGNC Symbol;Acc:HGNC:28949]"}, {"versioned_ensembl_gene_id":"ENSG00000281091.2","gene_symbol":"AL606763.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":103404777,"end":103408299,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213560.4","gene_symbol":"AC103591.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78091499,"end":78092054,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213561.4","gene_symbol":"AC103591.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":78043383,"end":78044148,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275571.2","gene_symbol":"TTC34","gene_name":"tetratricopeptide repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:34297]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100287898","summary":null,"start":2635571,"end":2801699,"strand":-1,"description":"tetratricopeptide repeat domain 34 [Source:HGNC Symbol;Acc:HGNC:34297]"}, {"versioned_ensembl_gene_id":"ENSG00000159079.18","gene_symbol":"C21orf59","gene_name":"chromosome 21 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:1301]","synonyms":"Kur,FLJ20467,FBB18,CILD26,C21orf48","biotype":"protein_coding","ncbi_id":"56683","summary":"This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]","start":32592079,"end":32612866,"strand":-1,"description":"chromosome 21 open reading frame 59 [Source:HGNC Symbol;Acc:HGNC:1301]"}, {"versioned_ensembl_gene_id":"ENSG00000273338.1","gene_symbol":"AC103591.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":78004346,"end":78004554,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234275.1","gene_symbol":"AC017053.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6312954,"end":6325646,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162616.8","gene_symbol":"DNAJB4","gene_name":"DnaJ heat shock protein family (Hsp40) member B4 [Source:HGNC Symbol;Acc:HGNC:14886]","synonyms":"HLJ1","biotype":"protein_coding","ncbi_id":"11080","summary":"The protein encoded by this gene is a molecular chaperone, tumor suppressor, and member of the heat shock protein-40 family. The encoded protein binds the cell adhesion protein E-cadherin and targets it to the plasma membrane. This protein also binds incorrectly folded E-cadherin and targets it for endoplasmic reticulum-associated degradation. This gene is a strong tumor suppressor for colorectal carcinoma, and downregulation of it may serve as a good biomarker for predicting patient outcomes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]","start":77979175,"end":78017964,"strand":1,"description":"DnaJ heat shock protein family (Hsp40) member B4 [Source:HGNC Symbol;Acc:HGNC:14886]"}, {"versioned_ensembl_gene_id":"ENSG00000172476.4","gene_symbol":"RAB40A","gene_name":"RAB40A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18283]","synonyms":"RAR2A,Rar-2","biotype":"protein_coding","ncbi_id":"142684","summary":"This gene encodes a member of the Rab40 subfamily of Rab small GTP-binding proteins that contains a C-terminal suppressors of cytokine signaling box. [provided by RefSeq, Apr 2010]","start":103499130,"end":103519489,"strand":-1,"description":"RAB40A, member RAS oncogene family [Source:HGNC Symbol;Acc:HGNC:18283]"}, {"versioned_ensembl_gene_id":"ENSG00000234405.1","gene_symbol":"Z69733.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":103497523,"end":103500317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163202.4","gene_symbol":"LCE3D","gene_name":"late cornified envelope 3D [Source:HGNC Symbol;Acc:HGNC:16615]","synonyms":"SPRL6A,LEP16,SPRL6B","biotype":"protein_coding","ncbi_id":"84648","summary":null,"start":152579381,"end":152580504,"strand":-1,"description":"late cornified envelope 3D [Source:HGNC Symbol;Acc:HGNC:16615]"}, {"versioned_ensembl_gene_id":"ENSG00000275290.4","gene_symbol":"LILRA2","gene_name":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]","synonyms":"LIR-7,ILT1,CD85h,LIR7","biotype":"protein_coding","ncbi_id":"11027","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]","start":54581134,"end":54595774,"strand":1,"description":"leukocyte immunoglobulin like receptor A2 [Source:HGNC Symbol;Acc:HGNC:6603]"}, {"versioned_ensembl_gene_id":"ENSG00000275125.4","gene_symbol":"FAM213B","gene_name":"family with sequence similarity 213 member B [Source:HGNC Symbol;Acc:HGNC:28390]","synonyms":"MGC26818,C1orf93","biotype":"protein_coding","ncbi_id":"127281","summary":null,"start":2586491,"end":2591469,"strand":1,"description":"family with sequence similarity 213 member B [Source:HGNC Symbol;Acc:HGNC:28390]"}, {"versioned_ensembl_gene_id":"ENSG00000244057.4","gene_symbol":"LCE3C","gene_name":"late cornified envelope 3C [Source:HGNC Symbol;Acc:HGNC:16612]","synonyms":"SPRL3A,LEP15","biotype":"protein_coding","ncbi_id":"353144","summary":null,"start":152600662,"end":152601086,"strand":1,"description":"late cornified envelope 3C [Source:HGNC Symbol;Acc:HGNC:16612]"}, {"versioned_ensembl_gene_id":"ENSG00000269058.5","gene_symbol":"CALR3","gene_name":"calreticulin 3 [Source:HGNC Symbol;Acc:HGNC:20407]","synonyms":"MGC26577,FLJ25355,CT93,CRT2","biotype":"protein_coding","ncbi_id":"125972","summary":"The protein encoded by this gene belongs to the calreticulin family, members of which are calcium-binding chaperones localized mainly in the endoplasmic reticulum. This protein is also localized to the endoplasmic reticulum lumen, however, its capacity for calcium-binding may be absent or much lower than other family members. This gene is specifically expressed in the testis, and may be required for sperm fertility. Mutation in this gene has been associated with familial hypertrophic cardiomyopathy. [provided by RefSeq, Dec 2011]","start":16479057,"end":16496192,"strand":-1,"description":"calreticulin 3 [Source:HGNC Symbol;Acc:HGNC:20407]"}, {"versioned_ensembl_gene_id":"ENSG00000232163.2","gene_symbol":"RPLP1P13","gene_name":"ribosomal protein lateral stalk subunit P1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:41973]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874124","summary":null,"start":23373423,"end":23374061,"strand":1,"description":"ribosomal protein lateral stalk subunit P1 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:41973]"}, {"versioned_ensembl_gene_id":"ENSG00000187238.5","gene_symbol":"LCE3B","gene_name":"late cornified envelope 3B [Source:HGNC Symbol;Acc:HGNC:29462]","synonyms":"LEP14","biotype":"protein_coding","ncbi_id":"353143","summary":null,"start":152613811,"end":152614098,"strand":1,"description":"late cornified envelope 3B [Source:HGNC Symbol;Acc:HGNC:29462]"}, {"versioned_ensembl_gene_id":"ENSG00000151835.14","gene_symbol":"SACS","gene_name":"sacsin molecular chaperone [Source:HGNC Symbol;Acc:HGNC:10519]","synonyms":"KIAA0730,DNAJC29,DKFZp686B15167,ARSACS,SPAX6,PPP1R138","biotype":"protein_coding","ncbi_id":"26278","summary":"This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. The authors of a publication on the effects of siRNA-mediated sacsin knockdown concluded that sacsin protects against mutant ataxin-1 and suggest that \"the large multi-domain sacsin protein is able to recruit Hsp70 chaperone action and has the potential to regulate the effects of other ataxia proteins\" (Parfitt et al., PubMed: 19208651). A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]","start":23328826,"end":23411513,"strand":-1,"description":"sacsin molecular chaperone [Source:HGNC Symbol;Acc:HGNC:10519]"}, {"versioned_ensembl_gene_id":"ENSG00000137960.5","gene_symbol":"GIPC2","gene_name":"GIPC PDZ domain containing family member 2 [Source:HGNC Symbol;Acc:HGNC:18177]","synonyms":"SEMCAP-2,FLJ20075","biotype":"protein_coding","ncbi_id":"54810","summary":null,"start":77979542,"end":78138449,"strand":1,"description":"GIPC PDZ domain containing family member 2 [Source:HGNC Symbol;Acc:HGNC:18177]"}, {"versioned_ensembl_gene_id":"ENSG00000250616.2","gene_symbol":"AC012645.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30096430,"end":30104116,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163646.10","gene_symbol":"CLRN1","gene_name":"clarin 1 [Source:HGNC Symbol;Acc:HGNC:12605]","synonyms":"RP61,USH3A,USH3","biotype":"protein_coding","ncbi_id":"7401","summary":"This gene encodes a protein that contains a cytosolic N-terminus, multiple helical transmembrane domains, and an endoplasmic reticulum membrane retention signal, TKGH, in the C-terminus. The encoded protein may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIIa. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]","start":150926163,"end":150972999,"strand":-1,"description":"clarin 1 [Source:HGNC Symbol;Acc:HGNC:12605]"}, {"versioned_ensembl_gene_id":"ENSG00000225903.1","gene_symbol":"AL035404.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":39633416,"end":39633903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237483.1","gene_symbol":"RPS27AP8","gene_name":"ribosomal protein S27a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36361]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271375","summary":null,"start":172225428,"end":172225872,"strand":-1,"description":"ribosomal protein S27a pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:36361]"}, {"versioned_ensembl_gene_id":"ENSG00000238278.3","gene_symbol":"ALG1L6P","gene_name":"asparagine-linked glycosylation 1-like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:44375]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"339879","summary":null,"start":75415070,"end":75422143,"strand":1,"description":"asparagine-linked glycosylation 1-like 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:44375]"}, {"versioned_ensembl_gene_id":"ENSG00000275801.1","gene_symbol":"AL121985.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160775954,"end":160776608,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163909.7","gene_symbol":"HEYL","gene_name":"hes related family bHLH transcription factor with YRPW motif-like [Source:HGNC Symbol;Acc:HGNC:4882]","synonyms":"HEY3,HESR3,bHLHb33","biotype":"protein_coding","ncbi_id":"26508","summary":"This gene encodes a member of the hairy and enhancer of split-related (HESR) family of basic helix-loop-helix (bHLH)-type transcription factors. The sequence of the encoded protein contains a conserved bHLH and orange domain, but its YRPW motif has diverged from other HESR family members. It is thought to be an effector of Notch signaling and a regulator of cell fate decisions. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]","start":39624153,"end":39639945,"strand":-1,"description":"hes related family bHLH transcription factor with YRPW motif-like [Source:HGNC Symbol;Acc:HGNC:4882]"}, {"versioned_ensembl_gene_id":"ENSG00000279862.1","gene_symbol":"AC092964.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":172301654,"end":172303052,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274562.1","gene_symbol":"AL121985.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":160776975,"end":160780140,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000075420.12","gene_symbol":"FNDC3B","gene_name":"fibronectin type III domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24670]","synonyms":"FLJ23399,FAD104,DKFZp762K137,YVTM2421,PRO4979","biotype":"protein_coding","ncbi_id":"64778","summary":null,"start":172039628,"end":172401665,"strand":1,"description":"fibronectin type III domain containing 3B [Source:HGNC Symbol;Acc:HGNC:24670]"}, {"versioned_ensembl_gene_id":"ENSG00000278102.1","gene_symbol":"AL138825.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18304854,"end":18305045,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223993.1","gene_symbol":"AC025428.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85431943,"end":85432515,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244026.6","gene_symbol":"FAM86DP","gene_name":"family with sequence similarity 86 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32659]","synonyms":"FAM86D","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"692099","summary":null,"start":75421552,"end":75435110,"strand":-1,"description":"family with sequence similarity 86 member D, pseudogene [Source:HGNC Symbol;Acc:HGNC:32659]"}, {"versioned_ensembl_gene_id":"ENSG00000217414.2","gene_symbol":"DDX18P3","gene_name":"DEAD-box helicase 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33966]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442164","summary":null,"start":18363417,"end":18365423,"strand":-1,"description":"DEAD-box helicase 18 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:33966]"}, {"versioned_ensembl_gene_id":"ENSG00000224652.1","gene_symbol":"LINC00885","gene_name":"long intergenic non-protein coding RNA 885 [Source:HGNC Symbol;Acc:HGNC:48571]","synonyms":null,"biotype":"lincRNA","ncbi_id":"401109","summary":null,"start":196142636,"end":196160890,"strand":1,"description":"long intergenic non-protein coding RNA 885 [Source:HGNC Symbol;Acc:HGNC:48571]"}, {"versioned_ensembl_gene_id":"ENSG00000218976.2","gene_symbol":"AL138725.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18366736,"end":18368644,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224504.2","gene_symbol":"AC025428.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":85432863,"end":85448961,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239428.2","gene_symbol":"GM2AP2","gene_name":"GM2 ganglioside activator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38002]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287900","summary":null,"start":171392229,"end":171392790,"strand":1,"description":"GM2 ganglioside activator pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:38002]"}, {"versioned_ensembl_gene_id":"ENSG00000237313.1","gene_symbol":"LINC01556","gene_name":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]","synonyms":"C6orf100,dJ25J6.5","biotype":"protein_coding","ncbi_id":"729583","summary":null,"start":28944039,"end":28944699,"strand":1,"description":"long intergenic non-protein coding RNA 1556 [Source:HGNC Symbol;Acc:HGNC:21195]"}, {"versioned_ensembl_gene_id":"ENSG00000122224.17","gene_symbol":"LY9","gene_name":"lymphocyte antigen 9 [Source:HGNC Symbol;Acc:HGNC:6730]","synonyms":"mLY9,hly9,CD229,SLAMF3","biotype":"protein_coding","ncbi_id":"4063","summary":"LY9 belongs to the SLAM family of immunomodulatory receptors (see SLAMF1; MIM 603492) and interacts with the adaptor molecule SAP (SH2D1A; MIM 300490) (Graham et al., 2006 [PubMed 16365421]).[supplied by OMIM, Mar 2008]","start":160796074,"end":160828261,"strand":1,"description":"lymphocyte antigen 9 [Source:HGNC Symbol;Acc:HGNC:6730]"}, {"versioned_ensembl_gene_id":"ENSG00000157368.10","gene_symbol":"IL34","gene_name":"interleukin 34 [Source:HGNC Symbol;Acc:HGNC:28529]","synonyms":"MGC34647,IL-34,C16orf77","biotype":"protein_coding","ncbi_id":"146433","summary":"Interleukin-34 is a cytokine that promotes the differentiation and viability of monocytes and macrophages through the colony-stimulating factor-1 receptor (CSF1R; MIM 164770) (Lin et al., 2008 [PubMed 18467591]).[supplied by OMIM, May 2008]","start":70579895,"end":70660682,"strand":1,"description":"interleukin 34 [Source:HGNC Symbol;Acc:HGNC:28529]"}, {"versioned_ensembl_gene_id":"ENSG00000141979.4","gene_symbol":"AC008764.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16479067,"end":16628204,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257985.1","gene_symbol":"AC004801.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48011304,"end":48025469,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257955.1","gene_symbol":"AC004801.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48019771,"end":48025382,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276814.1","gene_symbol":"AC004801.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":48039784,"end":48040761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214046.8","gene_symbol":"SMIM7","gene_name":"small integral membrane protein 7 [Source:HGNC Symbol;Acc:HGNC:28419]","synonyms":"MGC2747,C19orf42","biotype":"protein_coding","ncbi_id":"79086","summary":null,"start":16630751,"end":16660442,"strand":-1,"description":"small integral membrane protein 7 [Source:HGNC Symbol;Acc:HGNC:28419]"}, {"versioned_ensembl_gene_id":"ENSG00000157680.15","gene_symbol":"DGKI","gene_name":"diacylglycerol kinase iota [Source:HGNC Symbol;Acc:HGNC:2855]","synonyms":"DGK-IOTA","biotype":"protein_coding","ncbi_id":"9162","summary":"This gene is a member of the type IV diacylglycerol kinase subfamily. Diacylglycerol kinases regulate the intracellular concentration of diacylglycerol through its phosphorylation, producing phosphatidic acid. The specific role of the enzyme encoded by this gene is undetermined, however, it may play a crucial role in the production of phosphatidic acid in the retina or in recessive forms of retinal degeneration. [provided by RefSeq, Jul 2008]","start":137381037,"end":137847092,"strand":-1,"description":"diacylglycerol kinase iota [Source:HGNC Symbol;Acc:HGNC:2855]"}, {"versioned_ensembl_gene_id":"ENSG00000116981.3","gene_symbol":"NT5C1A","gene_name":"5'-nucleotidase, cytosolic IA [Source:HGNC Symbol;Acc:HGNC:17819]","synonyms":"MGC119201,MGC119199,CN1A,CN1,CN-IA,CN-I","biotype":"protein_coding","ncbi_id":"84618","summary":"Cytosolic nucleotidases, such as NT5C1A, dephosphorylate nucleoside monophosphates (Hunsucker et al., 2001 [PubMed 11133996]).[supplied by OMIM, Mar 2008]","start":39659121,"end":39672038,"strand":-1,"description":"5'-nucleotidase, cytosolic IA [Source:HGNC Symbol;Acc:HGNC:17819]"}, {"versioned_ensembl_gene_id":"ENSG00000204852.15","gene_symbol":"TCTN1","gene_name":"tectonic family member 1 [Source:HGNC Symbol;Acc:HGNC:26113]","synonyms":"TECT1,JBTS13,FLJ21127","biotype":"protein_coding","ncbi_id":"79600","summary":"This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]","start":110614027,"end":110649430,"strand":1,"description":"tectonic family member 1 [Source:HGNC Symbol;Acc:HGNC:26113]"}, {"versioned_ensembl_gene_id":"ENSG00000197056.9","gene_symbol":"ZMYM1","gene_name":"zinc finger MYM-type containing 1 [Source:HGNC Symbol;Acc:HGNC:26253]","synonyms":"MYM,FLJ23151","biotype":"protein_coding","ncbi_id":"79830","summary":null,"start":35059786,"end":35115859,"strand":1,"description":"zinc finger MYM-type containing 1 [Source:HGNC Symbol;Acc:HGNC:26253]"}, {"versioned_ensembl_gene_id":"ENSG00000179010.14","gene_symbol":"MRFAP1","gene_name":"Morf4 family associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24549]","synonyms":"PAM14,PGR1","biotype":"protein_coding","ncbi_id":"93621","summary":"This gene encodes an intracellular protein that interacts with members of the MORF4/MRG (mortality factor on chromosome 4/MORF4 related gene) family and the tumor suppressor Rb (retinoblastoma protein.) The protein may play a role in senescence, cell growth and immortalization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]","start":6640091,"end":6642745,"strand":1,"description":"Morf4 family associated protein 1 [Source:HGNC Symbol;Acc:HGNC:24549]"}, {"versioned_ensembl_gene_id":"ENSG00000029534.19","gene_symbol":"ANK1","gene_name":"ankyrin 1 [Source:HGNC Symbol;Acc:HGNC:492]","synonyms":"SPH1,ANK","biotype":"protein_coding","ncbi_id":"286","summary":"Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified. [provided by RefSeq, Dec 2008]","start":41653220,"end":41896762,"strand":-1,"description":"ankyrin 1 [Source:HGNC Symbol;Acc:HGNC:492]"}, {"versioned_ensembl_gene_id":"ENSG00000025434.18","gene_symbol":"NR1H3","gene_name":"nuclear receptor subfamily 1 group H member 3 [Source:HGNC Symbol;Acc:HGNC:7966]","synonyms":"RLD-1,LXR-a","biotype":"protein_coding","ncbi_id":"10062","summary":"The protein encoded by this gene belongs to the NR1 subfamily of the nuclear receptor superfamily. The NR1 family members are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. This protein is highly expressed in visceral organs, including liver, kidney and intestine. It forms a heterodimer with retinoid X receptor (RXR), and regulates expression of target genes containing retinoid response elements. Studies in mice lacking this gene suggest that it may play an important role in the regulation of cholesterol homeostasis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":47248300,"end":47269032,"strand":1,"description":"nuclear receptor subfamily 1 group H member 3 [Source:HGNC Symbol;Acc:HGNC:7966]"}, {"versioned_ensembl_gene_id":"ENSG00000103995.13","gene_symbol":"CEP152","gene_name":"centrosomal protein 152 [Source:HGNC Symbol;Acc:HGNC:29298]","synonyms":"SCKL5,MCPH9,KIAA0912","biotype":"protein_coding","ncbi_id":"22995","summary":"This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]","start":48712928,"end":48811146,"strand":-1,"description":"centrosomal protein 152 [Source:HGNC Symbol;Acc:HGNC:29298]"}, {"versioned_ensembl_gene_id":"ENSG00000214237.10","gene_symbol":"MINDY4B","gene_name":"MINDY family member 4B [Source:HGNC Symbol;Acc:HGNC:35475]","synonyms":"FAM188B2,C3orf76","biotype":"protein_coding","ncbi_id":"646951","summary":null,"start":150871045,"end":150905439,"strand":-1,"description":"MINDY family member 4B [Source:HGNC Symbol;Acc:HGNC:35475]"}, {"versioned_ensembl_gene_id":"ENSG00000136997.17","gene_symbol":"MYC","gene_name":"MYC proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7553]","synonyms":"MYCC,c-Myc,bHLHe39","biotype":"protein_coding","ncbi_id":"4609","summary":"This gene is a proto-oncogene and encodes a nuclear phosphoprotein that plays a role in cell cycle progression, apoptosis and cellular transformation. The encoded protein forms a heterodimer with the related transcription factor MAX. This complex binds to the E box DNA consensus sequence and regulates the transcription of specific target genes. Amplification of this gene is frequently observed in numerous human cancers. Translocations involving this gene are associated with Burkitt lymphoma and multiple myeloma in human patients. There is evidence to show that translation initiates both from an upstream, in-frame non-AUG (CUG) and a downstream AUG start site, resulting in the production of two isoforms with distinct N-termini. [provided by RefSeq, Aug 2017]","start":127735434,"end":127741434,"strand":1,"description":"MYC proto-oncogene, bHLH transcription factor [Source:HGNC Symbol;Acc:HGNC:7553]"}, {"versioned_ensembl_gene_id":"ENSG00000279400.1","gene_symbol":"AC008957.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":36667717,"end":36669958,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250155.1","gene_symbol":"AC008957.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36666214,"end":36725195,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079215.13","gene_symbol":"SLC1A3","gene_name":"solute carrier family 1 member 3 [Source:HGNC Symbol;Acc:HGNC:10941]","synonyms":"GLAST,EAAT1,EA6","biotype":"protein_coding","ncbi_id":"6507","summary":"This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]","start":36606355,"end":36688334,"strand":1,"description":"solute carrier family 1 member 3 [Source:HGNC Symbol;Acc:HGNC:10941]"}, {"versioned_ensembl_gene_id":"ENSG00000239265.5","gene_symbol":"CLRN1-AS1","gene_name":"CLRN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30895]","synonyms":"UCRP,CLRN1OS","biotype":"antisense_RNA","ncbi_id":"116933","summary":null,"start":150852484,"end":151080726,"strand":1,"description":"CLRN1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:30895]"}, {"versioned_ensembl_gene_id":"ENSG00000116983.12","gene_symbol":"HPCAL4","gene_name":"hippocalcin like 4 [Source:HGNC Symbol;Acc:HGNC:18212]","synonyms":"HLP4,DKFZp761G122","biotype":"protein_coding","ncbi_id":"51440","summary":"The protein encoded by this gene is highly similar to human hippocalcin protein and hippocalcin like-1 protein. It also has similarity to rat neural visinin-like Ca2+-binding protein-type 1 and 2 proteins. This encoded protein may be involved in the calcium-dependent regulation of rhodopsin phosphorylation. The transcript of this gene has multiple polyadenylation sites. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]","start":39678648,"end":39691689,"strand":-1,"description":"hippocalcin like 4 [Source:HGNC Symbol;Acc:HGNC:18212]"}, {"versioned_ensembl_gene_id":"ENSG00000260234.5","gene_symbol":"AC020636.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":150882997,"end":150941743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231467.2","gene_symbol":"AL022314.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":37080068,"end":37082847,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243273.1","gene_symbol":"AC020636.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":150890636,"end":151038818,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104371.4","gene_symbol":"DKK4","gene_name":"dickkopf WNT signaling pathway inhibitor 4 [Source:HGNC Symbol;Acc:HGNC:2894]","synonyms":null,"biotype":"protein_coding","ncbi_id":"27121","summary":"This gene encodes a protein that is a member of the dickkopf family. The secreted protein contains two cysteine rich regions and is involved in embryonic development through its interactions with the Wnt signaling pathway. Activity of this protein is modulated by binding to the Wnt co-receptor and the co-factor kremen 2. [provided by RefSeq, Jul 2008]","start":42374068,"end":42377232,"strand":-1,"description":"dickkopf WNT signaling pathway inhibitor 4 [Source:HGNC Symbol;Acc:HGNC:2894]"}, {"versioned_ensembl_gene_id":"ENSG00000236271.8","gene_symbol":"FLOT1","gene_name":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10211","summary":"This gene encodes an protein that localizes to the caveolae, which are small domains on the inner cell membranes. This protein plays a role in vesicle trafficking and cell morphology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","start":30772367,"end":30787391,"strand":-1,"description":"flotillin 1 [Source:HGNC Symbol;Acc:HGNC:3757]"}, {"versioned_ensembl_gene_id":"ENSG00000265349.1","gene_symbol":"AC118755.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9638768,"end":9645325,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271011.1","gene_symbol":"AC010680.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178577103,"end":178577622,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188175.9","gene_symbol":"HEPACAM2","gene_name":"HEPACAM family member 2 [Source:HGNC Symbol;Acc:HGNC:27364]","synonyms":"FLJ38683","biotype":"protein_coding","ncbi_id":"253012","summary":"This gene encodes a protein related to the immunoglobulin superfamily that plays a role in mitosis. Knockdown of this gene results in prometaphase arrest, abnormal nuclear morphology and apoptosis. Poly(ADP-ribosylation) of the encoded protein promotes its translocation to centrosomes, which may stimulate centrosome maturation. A chromosomal deletion including this gene may be associated with myeloid leukemia and myelodysplastic syndrome in human patients. [provided by RefSeq, Oct 2016]","start":93188586,"end":93226524,"strand":-1,"description":"HEPACAM family member 2 [Source:HGNC Symbol;Acc:HGNC:27364]"}, {"versioned_ensembl_gene_id":"ENSG00000265590.9","gene_symbol":"AP000275.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32578822,"end":32612281,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253793.1","gene_symbol":"AC008066.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30983459,"end":30984321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242220.6","gene_symbol":"TCP10L","gene_name":"t-complex 10 like [Source:HGNC Symbol;Acc:HGNC:11657]","synonyms":"PRED77","biotype":"protein_coding","ncbi_id":"140290","summary":null,"start":32574841,"end":32587373,"strand":-1,"description":"t-complex 10 like [Source:HGNC Symbol;Acc:HGNC:11657]"}, {"versioned_ensembl_gene_id":"ENSG00000235989.3","gene_symbol":"MORC2-AS1","gene_name":"MORC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26662]","synonyms":"NCRNA00325,FLJ35801,C22orf27","biotype":"antisense_RNA","ncbi_id":"150291","summary":null,"start":30922308,"end":30932449,"strand":1,"description":"MORC2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:26662]"}, {"versioned_ensembl_gene_id":"ENSG00000284641.1","gene_symbol":"AL139254.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20476222,"end":20478937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284743.1","gene_symbol":"AL139254.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":20478779,"end":20480397,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171843.15","gene_symbol":"MLLT3","gene_name":"MLLT3, super elongation complex subunit [Source:HGNC Symbol;Acc:HGNC:7136]","synonyms":"YEATS3,AF9,AF-9","biotype":"protein_coding","ncbi_id":"4300","summary":null,"start":20341665,"end":20622543,"strand":-1,"description":"MLLT3, super elongation complex subunit [Source:HGNC Symbol;Acc:HGNC:7136]"}, {"versioned_ensembl_gene_id":"ENSG00000253579.1","gene_symbol":"SUMO2P16","gene_name":"SUMO2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49354]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480679","summary":null,"start":31131539,"end":31131802,"strand":-1,"description":"SUMO2 pseudogene 16 [Source:HGNC Symbol;Acc:HGNC:49354]"}, {"versioned_ensembl_gene_id":"ENSG00000253961.1","gene_symbol":"AC009563.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31167078,"end":31177167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000124614.13","gene_symbol":"RPS10","gene_name":"ribosomal protein S10 [Source:HGNC Symbol;Acc:HGNC:10383]","synonyms":"S10,MGC88819","biotype":"protein_coding","ncbi_id":"6204","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S10E family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Alternate splicing results in multiple transcript variants that encode the same protein. Naturally occurring read-through transcription occurs between this locus and the neighboring locus NUDT3 (nudix (nucleoside diphosphate linked moiety X)-type motif 3).[provided by RefSeq, Feb 2011]","start":34417454,"end":34426125,"strand":-1,"description":"ribosomal protein S10 [Source:HGNC Symbol;Acc:HGNC:10383]"}, {"versioned_ensembl_gene_id":"ENSG00000102007.10","gene_symbol":"PLP2","gene_name":"proteolipid protein 2 [Source:HGNC Symbol;Acc:HGNC:9087]","synonyms":"A4,MGC126187,A4-LSB","biotype":"protein_coding","ncbi_id":"5355","summary":"This gene encodes an integral membrane protein that localizes to the endoplasmic reticulum in colonic epithelial cells. The encoded protein can multimerize and may function as an ion channel. A polymorphism in the promoter of this gene may be linked to an increased risk of X-linked cognitive disability. A pseudogene of this gene is found on chromosome 5. [provided by RefSeq, Jan 2010]","start":49171926,"end":49175239,"strand":1,"description":"proteolipid protein 2 [Source:HGNC Symbol;Acc:HGNC:9087]"}, {"versioned_ensembl_gene_id":"ENSG00000223584.1","gene_symbol":"TVP23CP1","gene_name":"TVP23C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44646]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421599","summary":null,"start":90631906,"end":90632568,"strand":1,"description":"TVP23C pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44646]"}, {"versioned_ensembl_gene_id":"ENSG00000172733.11","gene_symbol":"PURG","gene_name":"purine rich element binding protein G [Source:HGNC Symbol;Acc:HGNC:17930]","synonyms":"PURG-B,PURG-A","biotype":"protein_coding","ncbi_id":"29942","summary":"The exact function of this gene is not known, however, its encoded product is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. This gene lies in close proximity to the Werner syndrome gene, but on the opposite strand, on chromosome 8p11. [provided by RefSeq, Apr 2016]","start":30995802,"end":31033715,"strand":-1,"description":"purine rich element binding protein G [Source:HGNC Symbol;Acc:HGNC:17930]"}, {"versioned_ensembl_gene_id":"ENSG00000223969.5","gene_symbol":"AC002456.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":90590619,"end":90597353,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264619.6","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31825184,"end":31831870,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000280645.1","gene_symbol":"AC234231.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2632565,"end":2636215,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000165392.9","gene_symbol":"WRN","gene_name":"Werner syndrome RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:12791]","synonyms":"RECQ3,RECQL2","biotype":"protein_coding","ncbi_id":"7486","summary":"This gene encodes a member of the RecQ subfamily of DNA helicase proteins. The encoded nuclear protein is important in the maintenance of genome stability and plays a role in DNA repair, replication, transcription and telomere maintenance. This protein contains a N-terminal 3' to 5' exonuclease domain, an ATP-dependent helicase domain and RQC (RecQ helicase conserved region) domain in its central region, and a C-terminal HRDC (helicase RNase D C-terminal) domain and nuclear localization signal. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by accelerated aging and an elevated risk for certain cancers. [provided by RefSeq, Aug 2017]","start":31033801,"end":31173769,"strand":1,"description":"Werner syndrome RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:12791]"}, {"versioned_ensembl_gene_id":"ENSG00000232764.1","gene_symbol":"TRIM60P8Y","gene_name":"tripartite motif containing 60 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:38458]","synonyms":"TRIM60PY8,TRIM60P8","biotype":"processed_pseudogene","ncbi_id":"100420373","summary":null,"start":23025594,"end":23026663,"strand":1,"description":"tripartite motif containing 60 pseudogene 8, Y-linked [Source:HGNC Symbol;Acc:HGNC:38458]"}, {"versioned_ensembl_gene_id":"ENSG00000279483.2","gene_symbol":"AC090498.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137513859,"end":137513933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230383.1","gene_symbol":"AC009245.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":137721985,"end":137722846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233126.3","gene_symbol":"ZNF736P3Y","gene_name":"zinc finger protein 736 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:37728]","synonyms":"ZNF736P3,ZNF381P","biotype":"processed_pseudogene","ncbi_id":"246123","summary":null,"start":23049247,"end":23051195,"strand":1,"description":"zinc finger protein 736 pseudogene 3, Y-linked [Source:HGNC Symbol;Acc:HGNC:37728]"}, {"versioned_ensembl_gene_id":"ENSG00000225567.1","gene_symbol":"CR936923.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29026834,"end":29027761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215895.4","gene_symbol":"AL354702.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38708931,"end":38710890,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227251.1","gene_symbol":"TRIM60P9Y","gene_name":"tripartite motif containing 60 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:38459]","synonyms":"TRIM60PY9,TRIM60P9","biotype":"processed_pseudogene","ncbi_id":"100420374","summary":null,"start":23058030,"end":23059186,"strand":1,"description":"tripartite motif containing 60 pseudogene 9, Y-linked [Source:HGNC Symbol;Acc:HGNC:38459]"}, {"versioned_ensembl_gene_id":"ENSG00000267717.1","gene_symbol":"AC090330.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51158282,"end":51159383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186842.4","gene_symbol":"LINC00846","gene_name":"long intergenic non-protein coding RNA 846 [Source:HGNC Symbol;Acc:HGNC:16080]","synonyms":"C21orf77,FLJ10932","biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":32572238,"end":32575881,"strand":-1,"description":"long intergenic non-protein coding RNA 846 [Source:HGNC Symbol;Acc:HGNC:16080]"}, {"versioned_ensembl_gene_id":"ENSG00000006756.15","gene_symbol":"ARSD","gene_name":"arylsulfatase D [Source:HGNC Symbol;Acc:HGNC:717]","synonyms":null,"biotype":"protein_coding","ncbi_id":"414","summary":"The protein encoded by this gene is a member of the sulfatase family. Sulfatases are essential for the correct composition of bone and cartilage matrix. The encoded protein is postranslationally glycosylated and localized to the lysosome. This gene is located within a cluster of similar arylsulfatase genes on chromosome X. A related pseudogene has been identified in the pseudoautosomal region of chromosome Y. [provided by RefSeq, Jul 2011]","start":2903970,"end":2929351,"strand":-1,"description":"arylsulfatase D [Source:HGNC Symbol;Acc:HGNC:717]"}, {"versioned_ensembl_gene_id":"ENSG00000237298.9","gene_symbol":"TTN-AS1","gene_name":"TTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44124]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100506866","summary":"This gene encodes a non-coding RNA transcribed from the opposite strand to the titin gene. [provided by RefSeq, Aug 2016]","start":178521183,"end":178779963,"strand":1,"description":"TTN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44124]"}, {"versioned_ensembl_gene_id":"ENSG00000204915.3","gene_symbol":"AC234772.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45730752,"end":45731688,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176624.10","gene_symbol":"MEX3C","gene_name":"mex-3 RNA binding family member C [Source:HGNC Symbol;Acc:HGNC:28040]","synonyms":"RNF194,RKHD2,FLJ38871","biotype":"protein_coding","ncbi_id":"51320","summary":"This gene encodes a member of a family of proteins with two K homology (KH) RNA-binding domains and a C-terminal RING-finger domain. The protein interacts with mRNA via the KH domains, and the protein shuttles between the nucleus and cytoplasm. Polymorphisms in this gene may contribute to hypertension. [provided by RefSeq, Oct 2009]","start":51174550,"end":51218304,"strand":-1,"description":"mex-3 RNA binding family member C [Source:HGNC Symbol;Acc:HGNC:28040]"}, {"versioned_ensembl_gene_id":"ENSG00000236912.1","gene_symbol":"SAPCD1-AS1","gene_name":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]","synonyms":"C6orf26-AS1","biotype":"processed_transcript","ncbi_id":"104413891","summary":null,"start":31831329,"end":31832607,"strand":-1,"description":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]"}, {"versioned_ensembl_gene_id":"ENSG00000269902.1","gene_symbol":"AC234772.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45764772,"end":45765299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263179.1","gene_symbol":"HNRNPCP4","gene_name":"heterogeneous nuclear ribonucleoprotein C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48816]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421828","summary":null,"start":11242653,"end":11243552,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48816]"}, {"versioned_ensembl_gene_id":"ENSG00000233345.9","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31823611,"end":31830163,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000270069.1","gene_symbol":"MIR222HG","gene_name":"MIR222 host gene [Source:HGNC Symbol;Acc:HGNC:49555]","synonyms":"Lnc-Ang362","biotype":"lincRNA","ncbi_id":"104457406","summary":null,"start":45745211,"end":45770274,"strand":-1,"description":"MIR222 host gene [Source:HGNC Symbol;Acc:HGNC:49555]"}, {"versioned_ensembl_gene_id":"ENSG00000219738.2","gene_symbol":"CD83P1","gene_name":"CD83 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13946]","synonyms":"HB15p,CD83P,b34I8.3","biotype":"processed_pseudogene","ncbi_id":"100128240","summary":null,"start":27560822,"end":27561744,"strand":-1,"description":"CD83 molecule pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13946]"}, {"versioned_ensembl_gene_id":"ENSG00000281409.1","gene_symbol":"AF146191.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190041894,"end":190042377,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231566.1","gene_symbol":"AC234772.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45848074,"end":45851490,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000090432.6","gene_symbol":"MUL1","gene_name":"mitochondrial E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:25762]","synonyms":"RNF218,MULAN,MAPL,GIDE,FLJ12875,C1orf166","biotype":"protein_coding","ncbi_id":"79594","summary":null,"start":20499448,"end":20508161,"strand":-1,"description":"mitochondrial E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:25762]"}, {"versioned_ensembl_gene_id":"ENSG00000133142.17","gene_symbol":"TCEAL4","gene_name":"transcription elongation factor A like 4 [Source:HGNC Symbol;Acc:HGNC:26121]","synonyms":"WEX7,FLJ21174","biotype":"protein_coding","ncbi_id":"79921","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. This family is comprised of nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. Alternatively splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 13. [provided by RefSeq, Apr 2015]","start":103576231,"end":103587736,"strand":1,"description":"transcription elongation factor A like 4 [Source:HGNC Symbol;Acc:HGNC:26121]"}, {"versioned_ensembl_gene_id":"ENSG00000173295.7","gene_symbol":"FAM86B3P","gene_name":"family with sequence similarity 86 member B3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44371]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"286042","summary":null,"start":8228595,"end":8244865,"strand":1,"description":"family with sequence similarity 86 member B3, pseudogene [Source:HGNC Symbol;Acc:HGNC:44371]"}, {"versioned_ensembl_gene_id":"ENSG00000229054.1","gene_symbol":"RPS29P14","gene_name":"ribosomal protein S29 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36471]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129599","summary":null,"start":33036212,"end":33036382,"strand":-1,"description":"ribosomal protein S29 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:36471]"}, {"versioned_ensembl_gene_id":"ENSG00000248249.1","gene_symbol":"AC110794.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":175962061,"end":175962485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122643.18","gene_symbol":"NT5C3A","gene_name":"5'-nucleotidase, cytosolic IIIA [Source:HGNC Symbol;Acc:HGNC:17820]","synonyms":"p36,NT5C3,hUMP1,cN-III,UMPH1,UMPH,PSN1,POMP,PN-I,P5'N-1","biotype":"protein_coding","ncbi_id":"51251","summary":"This gene encodes a member of the 5'-nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5'-monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in this gene are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and pseudogenes of this gene are located on the long arm of chromosomes 3 and 4. [provided by RefSeq, Mar 2012]","start":33014114,"end":33062797,"strand":-1,"description":"5'-nucleotidase, cytosolic IIIA [Source:HGNC Symbol;Acc:HGNC:17820]"}, {"versioned_ensembl_gene_id":"ENSG00000163958.13","gene_symbol":"ZDHHC19","gene_name":"zinc finger DHHC-type containing 19 [Source:HGNC Symbol;Acc:HGNC:20713]","synonyms":"MGC33345","biotype":"protein_coding","ncbi_id":"131540","summary":null,"start":196197449,"end":196211437,"strand":-1,"description":"zinc finger DHHC-type containing 19 [Source:HGNC Symbol;Acc:HGNC:20713]"}, {"versioned_ensembl_gene_id":"ENSG00000249106.1","gene_symbol":"AC097537.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":175790307,"end":175812189,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000215520.3","gene_symbol":"RPS4XP4","gene_name":"ribosomal protein S4X pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36545]","synonyms":"RPS4P4","biotype":"processed_pseudogene","ncbi_id":"441878","summary":null,"start":20525989,"end":20526751,"strand":1,"description":"ribosomal protein S4X pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:36545]"}, {"versioned_ensembl_gene_id":"ENSG00000119147.9","gene_symbol":"C2orf40","gene_name":"chromosome 2 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:24642]","synonyms":"ECRG4,augurin","biotype":"protein_coding","ncbi_id":"84417","summary":null,"start":106063246,"end":106078159,"strand":1,"description":"chromosome 2 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:24642]"}, {"versioned_ensembl_gene_id":"ENSG00000183114.7","gene_symbol":"FAM43B","gene_name":"family with sequence similarity 43 member B [Source:HGNC Symbol;Acc:HGNC:31791]","synonyms":"FLJ44952","biotype":"protein_coding","ncbi_id":"163933","summary":null,"start":20552439,"end":20555010,"strand":1,"description":"family with sequence similarity 43 member B [Source:HGNC Symbol;Acc:HGNC:31791]"}, {"versioned_ensembl_gene_id":"ENSG00000166224.16","gene_symbol":"SGPL1","gene_name":"sphingosine-1-phosphate lyase 1 [Source:HGNC Symbol;Acc:HGNC:10817]","synonyms":"SPL","biotype":"protein_coding","ncbi_id":"8879","summary":null,"start":70815961,"end":70881173,"strand":1,"description":"sphingosine-1-phosphate lyase 1 [Source:HGNC Symbol;Acc:HGNC:10817]"}, {"versioned_ensembl_gene_id":"ENSG00000227115.7","gene_symbol":"LINC01630","gene_name":"long intergenic non-protein coding RNA 1630 [Source:HGNC Symbol;Acc:HGNC:52295]","synonyms":"LOC100287225","biotype":"lincRNA","ncbi_id":"100287225","summary":null,"start":51346249,"end":51643939,"strand":1,"description":"long intergenic non-protein coding RNA 1630 [Source:HGNC Symbol;Acc:HGNC:52295]"}, {"versioned_ensembl_gene_id":"ENSG00000253981.5","gene_symbol":"ALG1L13P","gene_name":"asparagine-linked glycosylation 1-like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:44382]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"106479038","summary":null,"start":8236003,"end":8244667,"strand":-1,"description":"asparagine-linked glycosylation 1-like 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:44382]"}, {"versioned_ensembl_gene_id":"ENSG00000164879.6","gene_symbol":"CA3","gene_name":"carbonic anhydrase 3 [Source:HGNC Symbol;Acc:HGNC:1374]","synonyms":"CAIII,Car3","biotype":"protein_coding","ncbi_id":"761","summary":"Carbonic anhydrase III (CAIII) is a member of a multigene family (at least six separate genes are known) that encodes carbonic anhydrase isozymes. These carbonic anhydrases are a class of metalloenzymes that catalyze the reversible hydration of carbon dioxide and are differentially expressed in a number of cell types. The expression of the CA3 gene is strictly tissue specific and present at high levels in skeletal muscle and much lower levels in cardiac and smooth muscle. A proportion of carriers of Duchenne muscle dystrophy have a higher CA3 level than normal. The gene spans 10.3 kb and contains seven exons and six introns. [provided by RefSeq, Oct 2008]","start":85373436,"end":85449040,"strand":1,"description":"carbonic anhydrase 3 [Source:HGNC Symbol;Acc:HGNC:1374]"}, {"versioned_ensembl_gene_id":"ENSG00000274441.1","gene_symbol":"AC008957.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":36636019,"end":36649347,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279322.1","gene_symbol":"AL035252.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":25226448,"end":25226735,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230962.1","gene_symbol":"LINC01520","gene_name":"long intergenic non-protein coding RNA 1520 [Source:HGNC Symbol;Acc:HGNC:51218]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929684","summary":null,"start":85449592,"end":85491996,"strand":1,"description":"long intergenic non-protein coding RNA 1520 [Source:HGNC Symbol;Acc:HGNC:51218]"}, {"versioned_ensembl_gene_id":"ENSG00000227007.1","gene_symbol":"LINC01247","gene_name":"long intergenic non-protein coding RNA 1247 [Source:HGNC Symbol;Acc:HGNC:49841]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101929390","summary":null,"start":6366010,"end":6375422,"strand":-1,"description":"long intergenic non-protein coding RNA 1247 [Source:HGNC Symbol;Acc:HGNC:49841]"}, {"versioned_ensembl_gene_id":"ENSG00000266201.1","gene_symbol":"SS18L2P2","gene_name":"SS18 like 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44966]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"724101","summary":null,"start":51421063,"end":51421674,"strand":-1,"description":"SS18 like 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44966]"}, {"versioned_ensembl_gene_id":"ENSG00000266003.1","gene_symbol":"AC109315.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51433437,"end":51434783,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197586.12","gene_symbol":"ENTPD6","gene_name":"ectonucleoside triphosphate diphosphohydrolase 6 (putative) [Source:HGNC Symbol;Acc:HGNC:3368]","synonyms":"NTPDase-6,IL6ST2,dJ738P15.3,CD39L2","biotype":"protein_coding","ncbi_id":"955","summary":"ENTPD6 is similar to E-type nucleotidases (NTPases). NTPases, such as CD39, mediate catabolism of extracellular nucleotides. ENTPD6 contains 4 apyrase-conserved regions which are characteristic of NTPases. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]","start":25195693,"end":25226729,"strand":1,"description":"ectonucleoside triphosphate diphosphohydrolase 6 (putative) [Source:HGNC Symbol;Acc:HGNC:3368]"}, {"versioned_ensembl_gene_id":"ENSG00000220583.1","gene_symbol":"RPL35P2","gene_name":"ribosomal protein L35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35789]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646766","summary":null,"start":34263311,"end":34263673,"strand":-1,"description":"ribosomal protein L35 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:35789]"}, {"versioned_ensembl_gene_id":"ENSG00000234333.2","gene_symbol":"CYCSP53","gene_name":"cytochrome c, somatic pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:24404]","synonyms":"HCP3","biotype":"processed_pseudogene","ncbi_id":"360156","summary":null,"start":171444699,"end":171444963,"strand":-1,"description":"cytochrome c, somatic pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:24404]"}, {"versioned_ensembl_gene_id":"ENSG00000272325.1","gene_symbol":"NUDT3","gene_name":"nudix hydrolase 3 [Source:HGNC Symbol;Acc:HGNC:8050]","synonyms":"DIPP","biotype":"protein_coding","ncbi_id":"11165","summary":"NUDT3 belongs to the MutT, or Nudix, protein family. Nudix proteins act as homeostatic checkpoints at important stages in nucleoside phosphate metabolic pathways, guarding against elevated levels of potentially dangerous intermediates, like 8-oxo-dGTP, which promotes AT-to-CG transversions (Safrany et al., 1998 [PubMed 9822604]).[supplied by OMIM, Feb 2011]","start":34279679,"end":34392674,"strand":-1,"description":"nudix hydrolase 3 [Source:HGNC Symbol;Acc:HGNC:8050]"}, {"versioned_ensembl_gene_id":"ENSG00000281173.1","gene_symbol":"ABCB10P1","gene_name":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]","synonyms":"ABCB10P,MABC2,M-ABC2,ABCB10P2","biotype":"processed_pseudogene","ncbi_id":"56476","summary":null,"start":23184646,"end":23186826,"strand":1,"description":"ATP binding cassette subfamily B member 10 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:14114]"}, {"versioned_ensembl_gene_id":"ENSG00000279910.1","gene_symbol":"AL731532.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85526880,"end":85531115,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280134.1","gene_symbol":"AL731532.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":85555484,"end":85557436,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226488.1","gene_symbol":"LINC01824","gene_name":"long intergenic non-protein coding RNA 1824 [Source:HGNC Symbol;Acc:HGNC:52630]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107985844","summary":null,"start":6496003,"end":6503806,"strand":1,"description":"long intergenic non-protein coding RNA 1824 [Source:HGNC Symbol;Acc:HGNC:52630]"}, {"versioned_ensembl_gene_id":"ENSG00000231610.1","gene_symbol":"PIK3CDP1","gene_name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52629]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"391349","summary":null,"start":6495877,"end":6496798,"strand":-1,"description":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52629]"}, {"versioned_ensembl_gene_id":"ENSG00000280490.1","gene_symbol":"AC116165.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23198268,"end":23198473,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281254.1","gene_symbol":"AC116165.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23219948,"end":23220085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188120.14","gene_symbol":"DAZ1","gene_name":"deleted in azoospermia 1 [Source:HGNC Symbol;Acc:HGNC:2682]","synonyms":"SPGY,DAZ","biotype":"protein_coding","ncbi_id":"1617","summary":"This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains three copies of the 10.8 kb repeat. However, no transcripts containing three copies of the RRM domain have been described; thus the RefSeq for this gene contains only two RRM domains. [provided by RefSeq, Jul 2008]","start":23129355,"end":23199094,"strand":-1,"description":"deleted in azoospermia 1 [Source:HGNC Symbol;Acc:HGNC:2682]"}, {"versioned_ensembl_gene_id":"ENSG00000281754.1","gene_symbol":"AC116165.10","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":23230653,"end":23231168,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000012211.12","gene_symbol":"PRICKLE3","gene_name":"prickle planar cell polarity protein 3 [Source:HGNC Symbol;Acc:HGNC:6645]","synonyms":"LMO6","biotype":"protein_coding","ncbi_id":"4007","summary":"LIM domain only 6 is a three LIM domain-containing protein. The LIM domain is a cysteine-rich sequence motif that binds zinc atoms to form a specific protein-binding interface for protein-protein interactions. [provided by RefSeq, Jul 2008]","start":49175264,"end":49186528,"strand":-1,"description":"prickle planar cell polarity protein 3 [Source:HGNC Symbol;Acc:HGNC:6645]"}, {"versioned_ensembl_gene_id":"ENSG00000227337.1","gene_symbol":"RPL23AP43","gene_name":"ribosomal protein L23a pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35751]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"389101","summary":null,"start":32785646,"end":32786116,"strand":1,"description":"ribosomal protein L23a pseudogene 43 [Source:HGNC Symbol;Acc:HGNC:35751]"}, {"versioned_ensembl_gene_id":"ENSG00000185015.7","gene_symbol":"CA13","gene_name":"carbonic anhydrase 13 [Source:HGNC Symbol;Acc:HGNC:14914]","synonyms":"MGC59868,FLJ37995,CAXIII","biotype":"protein_coding","ncbi_id":"377677","summary":"Carbonic anhydrases (CAs) are a family of zinc metalloenzymes. For background information on the CA family, see MIM 114800.[supplied by OMIM, Mar 2008]","start":85220587,"end":85284073,"strand":1,"description":"carbonic anhydrase 13 [Source:HGNC Symbol;Acc:HGNC:14914]"}, {"versioned_ensembl_gene_id":"ENSG00000186577.12","gene_symbol":"SMIM29","gene_name":"small integral membrane protein 29 [Source:HGNC Symbol;Acc:HGNC:1340]","synonyms":"C6orf1,MGC57858,LBH","biotype":"protein_coding","ncbi_id":"221491","summary":null,"start":34246380,"end":34249470,"strand":-1,"description":"small integral membrane protein 29 [Source:HGNC Symbol;Acc:HGNC:1340]"}, {"versioned_ensembl_gene_id":"ENSG00000234942.2","gene_symbol":"GRID1-AS1","gene_name":"GRID1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44131]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100507470","summary":null,"start":85577731,"end":85607213,"strand":1,"description":"GRID1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:44131]"}, {"versioned_ensembl_gene_id":"ENSG00000236606.1","gene_symbol":"AC022028.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":85708760,"end":85709167,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182771.18","gene_symbol":"GRID1","gene_name":"glutamate ionotropic receptor delta type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4575]","synonyms":"KIAA1220,GluD1","biotype":"protein_coding","ncbi_id":"2894","summary":"This gene encodes a subunit of glutamate receptor channels. These channels mediate most of the fast excitatory synaptic transmission in the central nervous system and play key roles in synaptic plasticity.[provided by RefSeq, Jan 2009]","start":85599555,"end":86366493,"strand":-1,"description":"glutamate ionotropic receptor delta type subunit 1 [Source:HGNC Symbol;Acc:HGNC:4575]"}, {"versioned_ensembl_gene_id":"ENSG00000268292.1","gene_symbol":"AC006547.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":20064552,"end":20065705,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281383.1","gene_symbol":"FP671120.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8254592,"end":8255514,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000106633.15","gene_symbol":"GCK","gene_name":"glucokinase [Source:HGNC Symbol;Acc:HGNC:4195]","synonyms":"MODY2,HK4","biotype":"protein_coding","ncbi_id":"2645","summary":"This gene encodes a member of the hexokinase family of proteins. Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. In contrast to other forms of hexokinase, this enzyme is not inhibited by its product glucose-6-phosphate but remains active while glucose is abundant. The use of multiple promoters and alternative splicing of this gene result in distinct protein isoforms that exhibit tissue-specific expression in the pancreas and liver. In the pancreas, this enzyme plays a role in glucose-stimulated insulin secretion, while in the liver, this enzyme is important in glucose uptake and conversion to glycogen. Mutations in this gene that alter enzyme activity have been associated with multiple types of diabetes and hyperinsulinemic hypoglycemia. [provided by RefSeq, Aug 2017]","start":44144271,"end":44198170,"strand":-1,"description":"glucokinase [Source:HGNC Symbol;Acc:HGNC:4195]"}, {"versioned_ensembl_gene_id":"ENSG00000010256.10","gene_symbol":"UQCRC1","gene_name":"ubiquinol-cytochrome c reductase core protein I [Source:HGNC Symbol;Acc:HGNC:12585]","synonyms":"UQCR1,QCR1,D3S3191","biotype":"protein_coding","ncbi_id":"7384","summary":null,"start":48599002,"end":48610976,"strand":-1,"description":"ubiquinol-cytochrome c reductase core protein I [Source:HGNC Symbol;Acc:HGNC:12585]"}, {"versioned_ensembl_gene_id":"ENSG00000250786.1","gene_symbol":"SNHG18","gene_name":"small nucleolar RNA host gene 18 [Source:HGNC Symbol;Acc:HGNC:49007]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100505806","summary":null,"start":9546200,"end":9550609,"strand":1,"description":"small nucleolar RNA host gene 18 [Source:HGNC Symbol;Acc:HGNC:49007]"}, {"versioned_ensembl_gene_id":"ENSG00000280441.2","gene_symbol":"FP236383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8380665,"end":8410645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170846.16","gene_symbol":"AC093323.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":6673451,"end":6676047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280614.1","gene_symbol":"FP236383.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8393419,"end":8394341,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281181.1","gene_symbol":"FP236383.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8437629,"end":8438551,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228027.1","gene_symbol":"AL136369.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11010164,"end":11011119,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251580.1","gene_symbol":"LINC02482","gene_name":"long intergenic non-protein coding RNA 2482 [Source:HGNC Symbol;Acc:HGNC:53458]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374366","summary":null,"start":6670725,"end":6673830,"strand":-1,"description":"long intergenic non-protein coding RNA 2482 [Source:HGNC Symbol;Acc:HGNC:53458]"}, {"versioned_ensembl_gene_id":"ENSG00000229792.1","gene_symbol":"LINC00399","gene_name":"long intergenic non-protein coding RNA 399 [Source:HGNC Symbol;Acc:HGNC:42728]","synonyms":"TCONS_00021596","biotype":"lincRNA","ncbi_id":"104326054","summary":null,"start":109400696,"end":109401641,"strand":1,"description":"long intergenic non-protein coding RNA 399 [Source:HGNC Symbol;Acc:HGNC:42728]"}, {"versioned_ensembl_gene_id":"ENSG00000230322.1","gene_symbol":"AL136320.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11168922,"end":11171376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235018.1","gene_symbol":"AL137077.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":62037429,"end":62037956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183688.4","gene_symbol":"RFLNB","gene_name":"refilin B [Source:HGNC Symbol;Acc:HGNC:28705]","synonyms":"FAM101B,Cfm1,RefilinB,MGC45871","biotype":"protein_coding","ncbi_id":"359845","summary":null,"start":439978,"end":445939,"strand":-1,"description":"refilin B [Source:HGNC Symbol;Acc:HGNC:28705]"}, {"versioned_ensembl_gene_id":"ENSG00000144857.14","gene_symbol":"BOC","gene_name":"BOC cell adhesion associated, oncogene regulated [Source:HGNC Symbol;Acc:HGNC:17173]","synonyms":"CDON2","biotype":"protein_coding","ncbi_id":"91653","summary":"The protein encoded by this gene is a member of the immunoglobulin/fibronectin type III repeat family. It is a component of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells, and promotes myogenic differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2014]","start":113211003,"end":113287459,"strand":1,"description":"BOC cell adhesion associated, oncogene regulated [Source:HGNC Symbol;Acc:HGNC:17173]"}, {"versioned_ensembl_gene_id":"ENSG00000229240.8","gene_symbol":"LINC00710","gene_name":"long intergenic non-protein coding RNA 710 [Source:HGNC Symbol;Acc:HGNC:27386]","synonyms":null,"biotype":"processed_transcript","ncbi_id":"254312","summary":null,"start":10917880,"end":10952234,"strand":-1,"description":"long intergenic non-protein coding RNA 710 [Source:HGNC Symbol;Acc:HGNC:27386]"}, {"versioned_ensembl_gene_id":"ENSG00000253549.5","gene_symbol":"CA3-AS1","gene_name":"CA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51657]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100996348","summary":null,"start":85441851,"end":85464915,"strand":-1,"description":"CA3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:51657]"}, {"versioned_ensembl_gene_id":"ENSG00000130699.18","gene_symbol":"TAF4","gene_name":"TATA-box binding protein associated factor 4 [Source:HGNC Symbol;Acc:HGNC:11537]","synonyms":"TAFII135,TAFII130,TAF4A,TAF2C1,TAF2C","biotype":"protein_coding","ncbi_id":"6874","summary":"Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is transcription factor IID (TFIID), which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes one of the larger subunits of TFIID that has been shown to potentiate transcriptional activation by retinoic acid, thyroid hormone and vitamin D3 receptors. In addition, this subunit interacts with the transcription factor CREB, which has a glutamine-rich activation domain, and binds to other proteins containing glutamine-rich regions. Aberrant binding to this subunit by proteins with expanded polyglutamine regions has been suggested as one of the pathogenetic mechanisms underlying a group of neurodegenerative disorders referred to as polyglutamine diseases. [provided by RefSeq, Jul 2008]","start":61953469,"end":62065810,"strand":-1,"description":"TATA-box binding protein associated factor 4 [Source:HGNC Symbol;Acc:HGNC:11537]"}, {"versioned_ensembl_gene_id":"ENSG00000234854.1","gene_symbol":"LINC00676","gene_name":"long intergenic non-protein coding RNA 676 [Source:HGNC Symbol;Acc:HGNC:44394]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"101409253","summary":null,"start":109728282,"end":109730007,"strand":1,"description":"long intergenic non-protein coding RNA 676 [Source:HGNC Symbol;Acc:HGNC:44394]"}, {"versioned_ensembl_gene_id":"ENSG00000104267.9","gene_symbol":"CA2","gene_name":"carbonic anhydrase 2 [Source:HGNC Symbol;Acc:HGNC:1373]","synonyms":"Car2,CAII,CA-II","biotype":"protein_coding","ncbi_id":"760","summary":"The protein encoded by this gene is one of several isozymes of carbonic anhydrase, which catalyzes reversible hydration of carbon dioxide. Defects in this enzyme are associated with osteopetrosis and renal tubular acidosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]","start":85463852,"end":85481493,"strand":1,"description":"carbonic anhydrase 2 [Source:HGNC Symbol;Acc:HGNC:1373]"}, {"versioned_ensembl_gene_id":"ENSG00000218682.1","gene_symbol":"AC064847.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":25856461,"end":25856966,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000237088.1","gene_symbol":"AL163193.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":20532552,"end":20533339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267474.1","gene_symbol":"AC008569.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":14458401,"end":14459366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123143.12","gene_symbol":"PKN1","gene_name":"protein kinase N1 [Source:HGNC Symbol;Acc:HGNC:9405]","synonyms":"DBK,PRKCL1,PRK1,PKN,PAK1,MGC46204","biotype":"protein_coding","ncbi_id":"5585","summary":"The protein encoded by this gene belongs to the protein kinase C superfamily. This kinase is activated by Rho family of small G proteins and may mediate the Rho-dependent signaling pathway. This kinase can be activated by phospholipids and by limited proteolysis. The 3-phosphoinositide dependent protein kinase-1 (PDPK1/PDK1) is reported to phosphorylate this kinase, which may mediate insulin signals to the actin cytoskeleton. The proteolytic activation of this kinase by caspase-3 or related proteases during apoptosis suggests its role in signal transduction related to apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":14433053,"end":14471867,"strand":1,"description":"protein kinase N1 [Source:HGNC Symbol;Acc:HGNC:9405]"}, {"versioned_ensembl_gene_id":"ENSG00000260809.1","gene_symbol":"VPS35P1","gene_name":"VPS35, retromer complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51805]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100422055","summary":null,"start":35090501,"end":35104834,"strand":1,"description":"VPS35, retromer complex component pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51805]"}, {"versioned_ensembl_gene_id":"ENSG00000143970.16","gene_symbol":"ASXL2","gene_name":"additional sex combs like 2, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:23805]","synonyms":"KIAA1685,FLJ10898,ASXH2","biotype":"protein_coding","ncbi_id":"55252","summary":"This gene encodes a member of a family of epigenetic regulators that bind various histone-modifying enzymes and are involved in the assembly of transcription factors at specific genomic loci. Naturally occurring mutations in this gene are associated with cancer in several tissue types (breast, bladder, pancreas, ovary, prostate, and blood). This gene plays an important role in neurodevelopment, cardiac function, adipogenesis, and osteoclastogenesis. [provided by RefSeq, Feb 2017]","start":25733753,"end":25878516,"strand":-1,"description":"additional sex combs like 2, transcriptional regulator [Source:HGNC Symbol;Acc:HGNC:23805]"}, {"versioned_ensembl_gene_id":"ENSG00000270002.1","gene_symbol":"AC022028.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85644073,"end":85648066,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256574.7","gene_symbol":"OR13A1","gene_name":"olfactory receptor family 13 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14772]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79290","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":45302298,"end":45315608,"strand":-1,"description":"olfactory receptor family 13 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:14772]"}, {"versioned_ensembl_gene_id":"ENSG00000259979.1","gene_symbol":"AC092133.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35118238,"end":35118956,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260724.1","gene_symbol":"AC023824.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35134514,"end":35135075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251215.1","gene_symbol":"GOLGA5P1","gene_name":"golgin A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43925]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418736","summary":null,"start":39169210,"end":39170335,"strand":-1,"description":"golgin A5 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43925]"}, {"versioned_ensembl_gene_id":"ENSG00000261800.1","gene_symbol":"AC023824.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35143722,"end":35144881,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179593.15","gene_symbol":"ALOX15B","gene_name":"arachidonate 15-lipoxygenase, type B [Source:HGNC Symbol;Acc:HGNC:434]","synonyms":"15-LOX-2","biotype":"protein_coding","ncbi_id":"247","summary":"This gene encodes a member of the lipoxygenase family of structurally related nonheme iron dioxygenases involved in the production of fatty acid hydroperoxides. The encoded protein converts arachidonic acid exclusively to 15S-hydroperoxyeicosatetraenoic acid, while metabolizing linoleic acid less effectively. This gene is located in a cluster of related genes and a pseudogene that spans approximately 100 kilobases on the short arm of chromosome 17. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":8039017,"end":8049134,"strand":1,"description":"arachidonate 15-lipoxygenase, type B [Source:HGNC Symbol;Acc:HGNC:434]"}, {"versioned_ensembl_gene_id":"ENSG00000082074.15","gene_symbol":"FYB1","gene_name":"FYN binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4036]","synonyms":"SLAP-130,FYB-120/130,FYB,ADAP","biotype":"protein_coding","ncbi_id":"2533","summary":"The protein encoded by this gene is an adapter for the FYN protein and LCP2 signaling cascades in T-cells. The encoded protein is involved in platelet activation and controls the expression of interleukin-2. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]","start":39105236,"end":39274528,"strand":-1,"description":"FYN binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4036]"}, {"versioned_ensembl_gene_id":"ENSG00000203878.11","gene_symbol":"CHIAP2","gene_name":"chitinase, acidic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44463]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"149620","summary":null,"start":111280059,"end":111286116,"strand":1,"description":"chitinase, acidic pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44463]"}, {"versioned_ensembl_gene_id":"ENSG00000269387.1","gene_symbol":"AL365205.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41764292,"end":41764460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163141.18","gene_symbol":"BNIPL","gene_name":"BCL2 interacting protein like [Source:HGNC Symbol;Acc:HGNC:16976]","synonyms":"PP753,BNIPL-2,BNIPl-1,BNIP-Sbeta,BNIP-Salpha,BNIP-S","biotype":"protein_coding","ncbi_id":"149428","summary":"The protein encoded by this gene interacts with several other proteins, such as BCL2, ARHGAP1, MIF and GFER. It may function as a bridge molecule between BCL2 and ARHGAP1/CDC42 in promoting cell death. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]","start":151036570,"end":151047600,"strand":1,"description":"BCL2 interacting protein like [Source:HGNC Symbol;Acc:HGNC:16976]"}, {"versioned_ensembl_gene_id":"ENSG00000235184.1","gene_symbol":"ZNF90P2","gene_name":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]","synonyms":"dJ111M5.3,ZNF463P","biotype":"processed_pseudogene","ncbi_id":"100419606","summary":null,"start":28889657,"end":28890731,"strand":-1,"description":"zinc finger protein 90 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:21687]"}, {"versioned_ensembl_gene_id":"ENSG00000230004.1","gene_symbol":"HCG14","gene_name":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]","synonyms":"dJ111M5.4","biotype":"processed_transcript","ncbi_id":"414760","summary":null,"start":28897348,"end":28898138,"strand":1,"description":"HLA complex group 14 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:18323]"}, {"versioned_ensembl_gene_id":"ENSG00000259125.1","gene_symbol":"LRP1-AS","gene_name":"LRP1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51694]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"105751187","summary":null,"start":57144620,"end":57147619,"strand":-1,"description":"LRP1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:51694]"}, {"versioned_ensembl_gene_id":"ENSG00000104325.6","gene_symbol":"DECR1","gene_name":"2,4-dienoyl-CoA reductase 1 [Source:HGNC Symbol;Acc:HGNC:2753]","synonyms":"SDR18C1,DECR","biotype":"protein_coding","ncbi_id":"1666","summary":"This gene encodes an accessory enzyme which participates in the beta-oxidation and metabolism of unsaturated fatty enoyl-CoA esters. [provided by RefSeq, Jul 2008]","start":90001405,"end":90052092,"strand":1,"description":"2,4-dienoyl-CoA reductase 1 [Source:HGNC Symbol;Acc:HGNC:2753]"}, {"versioned_ensembl_gene_id":"ENSG00000279598.1","gene_symbol":"AC009948.5","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":178554561,"end":178558966,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257283.1","gene_symbol":"AC012464.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":93894965,"end":93943603,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185962.1","gene_symbol":"LCE3A","gene_name":"late cornified envelope 3A [Source:HGNC Symbol;Acc:HGNC:29461]","synonyms":"LEP13","biotype":"protein_coding","ncbi_id":"353142","summary":null,"start":152622834,"end":152623103,"strand":-1,"description":"late cornified envelope 3A [Source:HGNC Symbol;Acc:HGNC:29461]"}, {"versioned_ensembl_gene_id":"ENSG00000270574.1","gene_symbol":"AC010680.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":178578790,"end":178580906,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271382.1","gene_symbol":"AC012464.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":93945041,"end":93947813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225339.3","gene_symbol":"AL354740.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":34248568,"end":34286768,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257915.1","gene_symbol":"GLULP5","gene_name":"glutamate-ammonia ligase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37989]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421694","summary":null,"start":114104542,"end":114105931,"strand":1,"description":"glutamate-ammonia ligase pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37989]"}, {"versioned_ensembl_gene_id":"ENSG00000134757.4","gene_symbol":"DSG3","gene_name":"desmoglein 3 [Source:HGNC Symbol;Acc:HGNC:3050]","synonyms":"CDHF6","biotype":"protein_coding","ncbi_id":"1830","summary":"This gene encodes a member of the desmoglein family and cadherin cell adhesion molecule superfamily of proteins. Desmogleins are calcium-binding transmembrane glycoprotein components of desmosomes, cell-cell junctions between epithelial, myocardial, and other cell types. The encoded preproprotein is proteolytically processed to generate the mature glycoprotein. This gene is present in a gene cluster with other desmoglein gene family members on chromosome 18. The encoded protein has been identified as the autoantigen of the autoimmune blistering disease pemphigus vulgaris. [provided by RefSeq, Jan 2016]","start":31447795,"end":31478702,"strand":1,"description":"desmoglein 3 [Source:HGNC Symbol;Acc:HGNC:3050]"}, {"versioned_ensembl_gene_id":"ENSG00000158825.5","gene_symbol":"CDA","gene_name":"cytidine deaminase [Source:HGNC Symbol;Acc:HGNC:1712]","synonyms":"CDD","biotype":"protein_coding","ncbi_id":"978","summary":"This gene encodes an enzyme involved in pyrimidine salvaging. The encoded protein forms a homotetramer that catalyzes the irreversible hydrolytic deamination of cytidine and deoxycytidine to uridine and deoxyuridine, respectively. It is one of several deaminases responsible for maintaining the cellular pyrimidine pool. Mutations in this gene are associated with decreased sensitivity to the cytosine nucleoside analogue cytosine arabinoside used in the treatment of certain childhood leukemias. [provided by RefSeq, Jul 2008]","start":20588948,"end":20618908,"strand":1,"description":"cytidine deaminase [Source:HGNC Symbol;Acc:HGNC:1712]"}, {"versioned_ensembl_gene_id":"ENSG00000226947.1","gene_symbol":"AL139247.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152644393,"end":152644717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176075.7","gene_symbol":"LINC00302","gene_name":"long intergenic non-protein coding RNA 302 [Source:HGNC Symbol;Acc:HGNC:31825]","synonyms":"XP33,NCRNA00302,C1orf46","biotype":"lincRNA","ncbi_id":"388699","summary":null,"start":152655477,"end":152656804,"strand":1,"description":"long intergenic non-protein coding RNA 302 [Source:HGNC Symbol;Acc:HGNC:31825]"}, {"versioned_ensembl_gene_id":"ENSG00000257360.1","gene_symbol":"AC123567.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94140077,"end":94141337,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277247.1","gene_symbol":"AC083809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":70570969,"end":70571440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257603.1","gene_symbol":"AC010183.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114077133,"end":114079902,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084093.16","gene_symbol":"REST","gene_name":"RE1 silencing transcription factor [Source:HGNC Symbol;Acc:HGNC:9966]","synonyms":"XBR,NRSF","biotype":"protein_coding","ncbi_id":"5978","summary":"This gene was initially identified as a transcriptional repressor that represses neuronal genes in non-neuronal tissues. However, depending on the cellular context, this gene can act as either an oncogene or a tumor suppressor. The encoded protein is a member of the Kruppel-type zinc finger transcription factor family. It represses transcription by binding a DNA sequence element called the neuron-restrictive silencer element. The protein is also found in undifferentiated neuronal progenitor cells and it is thought that this repressor may act as a master negative regulator of neurogenesis. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2018]","start":56907876,"end":56966678,"strand":1,"description":"RE1 silencing transcription factor [Source:HGNC Symbol;Acc:HGNC:9966]"}, {"versioned_ensembl_gene_id":"ENSG00000270800.2","gene_symbol":"RPS10-NUDT3","gene_name":"RPS10-NUDT3 readthrough [Source:HGNC Symbol;Acc:HGNC:49181]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529239","summary":"This locus represents naturally occurring read-through transcription between the neighboring RPS10 (ribosomal protein S10) and NUDT3 (nudix (nucleoside diphosphate linked moiety X)-type motif 3) genes on chromosome 6. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]","start":34284887,"end":34426071,"strand":-1,"description":"RPS10-NUDT3 readthrough [Source:HGNC Symbol;Acc:HGNC:49181]"}, {"versioned_ensembl_gene_id":"ENSG00000187223.3","gene_symbol":"LCE2D","gene_name":"late cornified envelope 2D [Source:HGNC Symbol;Acc:HGNC:16518]","synonyms":"SPRL1A,LEP12","biotype":"protein_coding","ncbi_id":"353141","summary":null,"start":152663396,"end":152664659,"strand":1,"description":"late cornified envelope 2D [Source:HGNC Symbol;Acc:HGNC:16518]"}, {"versioned_ensembl_gene_id":"ENSG00000142765.17","gene_symbol":"SYTL1","gene_name":"synaptotagmin like 1 [Source:HGNC Symbol;Acc:HGNC:15584]","synonyms":"SLP1,JFC1,FLJ14996,exophilin-7","biotype":"protein_coding","ncbi_id":"84958","summary":null,"start":27342020,"end":27353937,"strand":1,"description":"synaptotagmin like 1 [Source:HGNC Symbol;Acc:HGNC:15584]"}, {"versioned_ensembl_gene_id":"ENSG00000263015.1","gene_symbol":"AC015853.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":503171,"end":511347,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000123384.13","gene_symbol":"LRP1","gene_name":"LDL receptor related protein 1 [Source:HGNC Symbol;Acc:HGNC:6692]","synonyms":"APR,APOER,A2MR,LRP1A,LRP,CD91","biotype":"protein_coding","ncbi_id":"4035","summary":"This gene encodes a member of the low-density lipoprotein receptor family of proteins. The encoded preproprotein is proteolytically processed by furin to generate 515 kDa and 85 kDa subunits that form the mature receptor (PMID: 8546712). This receptor is involved in several cellular processes, including intracellular signaling, lipid homeostasis, and clearance of apoptotic cells. In addition, the encoded protein is necessary for the alpha 2-macroglobulin-mediated clearance of secreted amyloid precursor protein and beta-amyloid, the main component of amyloid plaques found in Alzheimer patients. Expression of this gene decreases with age and has been found to be lower than controls in brain tissue from Alzheimer's disease patients. [provided by RefSeq, Oct 2015]","start":57128493,"end":57213351,"strand":1,"description":"LDL receptor related protein 1 [Source:HGNC Symbol;Acc:HGNC:6692]"}, {"versioned_ensembl_gene_id":"ENSG00000262905.1","gene_symbol":"AC015853.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":552566,"end":553417,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262708.1","gene_symbol":"AC027455.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":616002,"end":616595,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257962.1","gene_symbol":"AC011773.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85246295,"end":85249848,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263300.1","gene_symbol":"AC015853.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":523140,"end":540576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261703.1","gene_symbol":"LINC02168","gene_name":"long intergenic non-protein coding RNA 2168 [Source:HGNC Symbol;Acc:HGNC:53030]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371252","summary":null,"start":50806668,"end":50807629,"strand":1,"description":"long intergenic non-protein coding RNA 2168 [Source:HGNC Symbol;Acc:HGNC:53030]"}, {"versioned_ensembl_gene_id":"ENSG00000244097.1","gene_symbol":"RPS4XP17","gene_name":"ribosomal protein S4X pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36789]","synonyms":"RPS4P17","biotype":"processed_pseudogene","ncbi_id":"100128140","summary":null,"start":656794,"end":657547,"strand":-1,"description":"ribosomal protein S4X pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36789]"}, {"versioned_ensembl_gene_id":"ENSG00000133742.13","gene_symbol":"CA1","gene_name":"carbonic anhydrase 1 [Source:HGNC Symbol;Acc:HGNC:1368]","synonyms":"Car1","biotype":"protein_coding","ncbi_id":"759","summary":"Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. This CA1 gene is closely linked to the CA2 and CA3 genes on chromosome 8. It encodes a cytosolic protein that is found at the highest level in erythrocytes. Allelic variants of this gene have been described in some populations. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Nov 2016]","start":85327608,"end":85379014,"strand":-1,"description":"carbonic anhydrase 1 [Source:HGNC Symbol;Acc:HGNC:1368]"}, {"versioned_ensembl_gene_id":"ENSG00000141252.19","gene_symbol":"VPS53","gene_name":"VPS53, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:25608]","synonyms":"HCCS1,FLJ10979","biotype":"protein_coding","ncbi_id":"55275","summary":"This gene encodes a protein with sequence similarity to the yeast Vps53p protein. Vps53p is involved in retrograde vesicle trafficking in late Golgi. [provided by RefSeq, Jul 2008]","start":508668,"end":721717,"strand":-1,"description":"VPS53, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:25608]"}, {"versioned_ensembl_gene_id":"ENSG00000257997.5","gene_symbol":"AC010183.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":114080381,"end":114113489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257300.1","gene_symbol":"HAUS8P1","gene_name":"HAUS augmin like complex subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43766]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420901","summary":null,"start":114097682,"end":114098223,"strand":1,"description":"HAUS augmin like complex subunit 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:43766]"}, {"versioned_ensembl_gene_id":"ENSG00000217643.1","gene_symbol":"PTGES3P2","gene_name":"prostaglandin E synthase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43822]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"101929293","summary":null,"start":25822469,"end":25822950,"strand":1,"description":"prostaglandin E synthase 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43822]"}, {"versioned_ensembl_gene_id":"ENSG00000187180.3","gene_symbol":"LCE2C","gene_name":"late cornified envelope 2C [Source:HGNC Symbol;Acc:HGNC:29460]","synonyms":"LEP11","biotype":"protein_coding","ncbi_id":"353140","summary":null,"start":152675295,"end":152676574,"strand":1,"description":"late cornified envelope 2C [Source:HGNC Symbol;Acc:HGNC:29460]"}, {"versioned_ensembl_gene_id":"ENSG00000279990.1","gene_symbol":"RPSAP68","gene_name":"ribosomal protein SA pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:51920]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100996520","summary":null,"start":8603547,"end":8603984,"strand":1,"description":"ribosomal protein SA pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:51920]"}, {"versioned_ensembl_gene_id":"ENSG00000279615.1","gene_symbol":"CR381572.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8680538,"end":8680934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278501.2","gene_symbol":"TIMM22","gene_name":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]","synonyms":"TIM22,TEX4","biotype":"protein_coding","ncbi_id":"29928","summary":"Multipass transmembrane proteins are brought into mitochondria and inserted into the mitochondrial inner membrane by way of the TIM22 complex. This complex has six subunits and is a twin-pore translocase. The protein encoded by this gene is a subunit of TIM22 and represents the voltage-activated and signal-gated channel. [provided by RefSeq, Jul 2016]","start":997117,"end":1003671,"strand":1,"description":"translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317]"}, {"versioned_ensembl_gene_id":"ENSG00000279167.1","gene_symbol":"CR381572.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":8701461,"end":8701562,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257444.1","gene_symbol":"SETP7","gene_name":"SET pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42926]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873166","summary":null,"start":107271394,"end":107271846,"strand":1,"description":"SET pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42926]"}, {"versioned_ensembl_gene_id":"ENSG00000206394.8","gene_symbol":"CLIC1","gene_name":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]","synonyms":"G6,p64CLCP,NCC27","biotype":"protein_coding","ncbi_id":"1192","summary":"Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 1 is a member of the p64 family; the protein localizes principally to the cell nucleus and exhibits both nuclear and plasma membrane chloride ion channel activity. [provided by RefSeq, Jul 2008]","start":31720799,"end":31729989,"strand":-1,"description":"chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]"}, {"versioned_ensembl_gene_id":"ENSG00000081479.12","gene_symbol":"LRP2","gene_name":"LDL receptor related protein 2 [Source:HGNC Symbol;Acc:HGNC:6694]","synonyms":"gp330,DBS","biotype":"protein_coding","ncbi_id":"4036","summary":"The protein encoded by this gene, low density lipoprotein-related protein 2 (LRP2) or megalin, is a multi-ligand endocytic receptor that is expressed in many different tissues but primarily in absorptive epithilial tissues such as the kidney. This glycoprotein has a large amino-terminal extracellular domain, a single transmembrane domain, and a short carboxy-terminal cytoplasmic tail. The extracellular ligand-binding-domains bind diverse macromolecules including albumin, apolipoproteins B and E, and lipoprotein lipase. The LRP2 protein is critical for the reuptake of numerous ligands, including lipoproteins, sterols, vitamin-binding proteins, and hormones. This protein also has a role in cell-signaling; extracellular ligands include parathyroid horomones and the morphogen sonic hedgehog while cytosolic ligands include MAP kinase scaffold proteins and JNK interacting proteins. Recycling of this membrane receptor is regulated by phosphorylation of its cytoplasmic domain. Mutations in this gene cause Donnai-Barrow syndrome (DBS) and facio-oculoacoustico-renal syndrome (FOAR).[provided by RefSeq, Aug 2009]","start":169127109,"end":169362685,"strand":-1,"description":"LDL receptor related protein 2 [Source:HGNC Symbol;Acc:HGNC:6694]"}, {"versioned_ensembl_gene_id":"ENSG00000238120.1","gene_symbol":"LINC01589","gene_name":"long intergenic non-protein coding RNA 1589 [Source:HGNC Symbol;Acc:HGNC:51520]","synonyms":"TCONS_00029353,CTA-941F9.9","biotype":"antisense_RNA","ncbi_id":"100506737","summary":null,"start":45604432,"end":45605621,"strand":-1,"description":"long intergenic non-protein coding RNA 1589 [Source:HGNC Symbol;Acc:HGNC:51520]"}, {"versioned_ensembl_gene_id":"ENSG00000260244.1","gene_symbol":"AC104083.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":155734448,"end":155737062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229558.2","gene_symbol":"SACS-AS1","gene_name":"SACS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39835]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506680","summary":null,"start":23418971,"end":23428869,"strand":1,"description":"SACS antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39835]"}, {"versioned_ensembl_gene_id":"ENSG00000213480.3","gene_symbol":"AC093816.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":121369433,"end":121370345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000186867.10","gene_symbol":"QRFPR","gene_name":"pyroglutamylated RFamide peptide receptor [Source:HGNC Symbol;Acc:HGNC:15565]","synonyms":"GPR103","biotype":"protein_coding","ncbi_id":"84109","summary":null,"start":121329312,"end":121381059,"strand":-1,"description":"pyroglutamylated RFamide peptide receptor [Source:HGNC Symbol;Acc:HGNC:15565]"}, {"versioned_ensembl_gene_id":"ENSG00000137221.14","gene_symbol":"TJAP1","gene_name":"tight junction associated protein 1 [Source:HGNC Symbol;Acc:HGNC:17949]","synonyms":"TJP4,PILT","biotype":"protein_coding","ncbi_id":"93643","summary":"This gene encodes a tight junction-associated protein. Incorporation of the encoded protein into tight junctions occurs at a late stage of formation of the junctions. The encoded protein localizes to the Golgi and may function in vesicle trafficking. Alternatively spliced transcript variants have been described. A related pseudogene exists on the X chromosome. [provided by RefSeq, Mar 2009]","start":43477523,"end":43506556,"strand":1,"description":"tight junction associated protein 1 [Source:HGNC Symbol;Acc:HGNC:17949]"}, {"versioned_ensembl_gene_id":"ENSG00000248334.6","gene_symbol":"WHAMMP2","gene_name":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32360]","synonyms":"WHDC1L2,WHAMML2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"440253","summary":null,"start":28737583,"end":28759204,"strand":1,"description":"WAS protein homolog associated with actin, golgi membranes and microtubules pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:32360]"}, {"versioned_ensembl_gene_id":"ENSG00000164116.16","gene_symbol":"GUCY1A3","gene_name":"guanylate cyclase 1 soluble subunit alpha [Source:HGNC Symbol;Acc:HGNC:4685]","synonyms":"GUC1A3,GC-SA3","biotype":"protein_coding","ncbi_id":"2982","summary":"Soluble guanylate cyclases are heterodimeric proteins that catalyze the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. The protein encoded by this gene is an alpha subunit of this complex and it interacts with a beta subunit to form the guanylate cyclase enzyme, which is activated by nitric oxide. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":155666711,"end":155732349,"strand":1,"description":"guanylate cyclase 1 soluble subunit alpha [Source:HGNC Symbol;Acc:HGNC:4685]"}, {"versioned_ensembl_gene_id":"ENSG00000240751.1","gene_symbol":"AC026348.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":113360267,"end":113361319,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166780.10","gene_symbol":"C16orf45","gene_name":"chromosome 16 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:19213]","synonyms":"FLJ32618","biotype":"protein_coding","ncbi_id":"89927","summary":null,"start":15434295,"end":15625028,"strand":1,"description":"chromosome 16 open reading frame 45 [Source:HGNC Symbol;Acc:HGNC:19213]"}, {"versioned_ensembl_gene_id":"ENSG00000206530.10","gene_symbol":"CFAP44","gene_name":"cilia and flagella associated protein 44 [Source:HGNC Symbol;Acc:HGNC:25631]","synonyms":"WDR52,FLJ11142","biotype":"protein_coding","ncbi_id":"55779","summary":null,"start":113286947,"end":113441610,"strand":-1,"description":"cilia and flagella associated protein 44 [Source:HGNC Symbol;Acc:HGNC:25631]"}, {"versioned_ensembl_gene_id":"ENSG00000272657.1","gene_symbol":"AP000317.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":34073592,"end":34360033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198743.6","gene_symbol":"SLC5A3","gene_name":"solute carrier family 5 member 3 [Source:HGNC Symbol;Acc:HGNC:11038]","synonyms":"SMIT1,SMIT","biotype":"protein_coding","ncbi_id":"6526","summary":null,"start":34073570,"end":34106262,"strand":1,"description":"solute carrier family 5 member 3 [Source:HGNC Symbol;Acc:HGNC:11038]"}, {"versioned_ensembl_gene_id":"ENSG00000215286.3","gene_symbol":"AL031584.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45913118,"end":45913871,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234613.1","gene_symbol":"AL031584.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":45913267,"end":45917040,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224701.1","gene_symbol":"MED28P4","gene_name":"mediator complex subunit 28 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45081]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130359","summary":null,"start":45951762,"end":45952333,"strand":-1,"description":"mediator complex subunit 28 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45081]"}, {"versioned_ensembl_gene_id":"ENSG00000261684.1","gene_symbol":"AC018362.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":42531867,"end":42532840,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235347.1","gene_symbol":"Z84478.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":45792418,"end":45793636,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243927.5","gene_symbol":"MRPS6","gene_name":"mitochondrial ribosomal protein S6 [Source:HGNC Symbol;Acc:HGNC:14051]","synonyms":"C21orf101,RPMS6,MRP-S6","biotype":"protein_coding","ncbi_id":"64968","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S6P family. Pseudogenes corresponding to this gene are found on chromosomes 1p and 12q. [provided by RefSeq, Jul 2008]","start":34073224,"end":34143034,"strand":1,"description":"mitochondrial ribosomal protein S6 [Source:HGNC Symbol;Acc:HGNC:14051]"}, {"versioned_ensembl_gene_id":"ENSG00000280383.1","gene_symbol":"Z95331.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":45657019,"end":45680130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130638.16","gene_symbol":"ATXN10","gene_name":"ataxin 10 [Source:HGNC Symbol;Acc:HGNC:10549]","synonyms":"SCA10,FLJ37990,E46L","biotype":"protein_coding","ncbi_id":"25814","summary":"This gene encodes a protein that may function in neuron survival, neuron differentiation, and neuritogenesis. These roles may be carried out via activation of the mitogen-activated protein kinase cascade. Expansion of an ATTCT repeat from 9-32 copies to 800-4500 copies in an intronic region of this locus has been associated with spinocerebellar ataxia, type 10. Alternatively spliced transcript variants have been described.[provided by RefSeq, Jul 2016]","start":45671798,"end":45845307,"strand":1,"description":"ataxin 10 [Source:HGNC Symbol;Acc:HGNC:10549]"}, {"versioned_ensembl_gene_id":"ENSG00000092531.9","gene_symbol":"SNAP23","gene_name":"synaptosome associated protein 23 [Source:HGNC Symbol;Acc:HGNC:11131]","synonyms":"SNAP23B,SNAP23A,HsT17016","biotype":"protein_coding","ncbi_id":"8773","summary":"Specificity of vesicular transport is regulated, in part, by the interaction of a vesicle-associated membrane protein termed synaptobrevin/VAMP with a target compartment membrane protein termed syntaxin. These proteins, together with SNAP25 (synaptosome-associated protein of 25 kDa), form a complex which serves as a binding site for the general membrane fusion machinery. Synaptobrevin/VAMP and syntaxin are believed to be involved in vesicular transport in most, if not all cells, while SNAP25 is present almost exclusively in the brain, suggesting that a ubiquitously expressed homolog of SNAP25 exists to facilitate transport vesicle/target membrane fusion in other tissues. The protein encoded by this gene is structurally and functionally similar to SNAP25 and binds tightly to multiple syntaxins and synaptobrevins/VAMPs. It is an essential component of the high affinity receptor for the general membrane fusion machinery and is an important regulator of transport vesicle docking and fusion. Two alternative transcript variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":42491233,"end":42545356,"strand":1,"description":"synaptosome associated protein 23 [Source:HGNC Symbol;Acc:HGNC:11131]"}, {"versioned_ensembl_gene_id":"ENSG00000188626.6","gene_symbol":"GOLGA8M","gene_name":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653720","summary":null,"start":28701954,"end":28738384,"strand":-1,"description":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]"}, {"versioned_ensembl_gene_id":"ENSG00000167968.12","gene_symbol":"DNASE1L2","gene_name":"deoxyribonuclease 1 like 2 [Source:HGNC Symbol;Acc:HGNC:2958]","synonyms":"DNAS1L2","biotype":"protein_coding","ncbi_id":"1775","summary":null,"start":2235816,"end":2238711,"strand":1,"description":"deoxyribonuclease 1 like 2 [Source:HGNC Symbol;Acc:HGNC:2958]"}, {"versioned_ensembl_gene_id":"ENSG00000083444.16","gene_symbol":"PLOD1","gene_name":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:9081]","synonyms":"PLOD,LLH,LH1","biotype":"protein_coding","ncbi_id":"5351","summary":"Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]","start":11934205,"end":11975538,"strand":1,"description":"procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 [Source:HGNC Symbol;Acc:HGNC:9081]"}, {"versioned_ensembl_gene_id":"ENSG00000224598.1","gene_symbol":"RPS5P2","gene_name":"ribosomal protein S5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17222]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130240","summary":null,"start":34135432,"end":34136071,"strand":-1,"description":"ribosomal protein S5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:17222]"}, {"versioned_ensembl_gene_id":"ENSG00000266442.5","gene_symbol":"MSH5-SAPCD1","gene_name":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]","synonyms":"MSH5-C6orf26","biotype":"protein_coding","ncbi_id":"100532732","summary":"This locus represents naturally occurring read-through transcription between the neighboring mutS homolog 5 (MSH5) and chromosome 6 open reading frame 26 (C6orf26) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]","start":31816303,"end":31841147,"strand":1,"description":"MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]"}, {"versioned_ensembl_gene_id":"ENSG00000227456.7","gene_symbol":"LINC00310","gene_name":"long intergenic non-protein coding RNA 310 [Source:HGNC Symbol;Acc:HGNC:16414]","synonyms":"NCRNA00310,C21orf82","biotype":"lincRNA","ncbi_id":"114036","summary":null,"start":34157724,"end":34190244,"strand":1,"description":"long intergenic non-protein coding RNA 310 [Source:HGNC Symbol;Acc:HGNC:16414]"}, {"versioned_ensembl_gene_id":"ENSG00000261480.1","gene_symbol":"GOLGA8M","gene_name":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]","synonyms":null,"biotype":"lincRNA","ncbi_id":"653720","summary":null,"start":28719377,"end":28738431,"strand":-1,"description":"golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]"}, {"versioned_ensembl_gene_id":"ENSG00000107897.18","gene_symbol":"ACBD5","gene_name":"acyl-CoA binding domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23338]","synonyms":"KIAA1996,DKFZp434A2417","biotype":"protein_coding","ncbi_id":"91452","summary":"This gene encodes a member of the acyl-Coenzyme A binding protein family, known to function in the transport and distribution of long chain acyl-Coenzyme A in cells. This gene may play a role in the differentiation of megakaryocytes and formation of platelets. A related protein in yeast is involved in autophagy of peroxisomes. A mutation in this gene has been associated with autosomal dominant thrombocytopenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":27195214,"end":27242130,"strand":-1,"description":"acyl-CoA binding domain containing 5 [Source:HGNC Symbol;Acc:HGNC:23338]"}, {"versioned_ensembl_gene_id":"ENSG00000279579.3","gene_symbol":"LINC01666","gene_name":"long intergenic non-protein coding RNA 1666 [Source:HGNC Symbol;Acc:HGNC:52454]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105372730","summary":null,"start":8759077,"end":8761335,"strand":1,"description":"long intergenic non-protein coding RNA 1666 [Source:HGNC Symbol;Acc:HGNC:52454]"}, {"versioned_ensembl_gene_id":"ENSG00000214955.5","gene_symbol":"AP000317.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":34205055,"end":34325034,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279213.1","gene_symbol":"SNX18P10","gene_name":"sorting nexin 18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100419040","summary":null,"start":8801362,"end":8801880,"strand":-1,"description":"sorting nexin 18 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:39618]"}, {"versioned_ensembl_gene_id":"ENSG00000237276.8","gene_symbol":"ANO7L1","gene_name":"anoctamin 7 like 1 [Source:HGNC Symbol;Acc:HGNC:32248]","synonyms":"C1orf224,ANO7P1,TMEM16M","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"101927546","summary":null,"start":16215909,"end":16228027,"strand":-1,"description":"anoctamin 7 like 1 [Source:HGNC Symbol;Acc:HGNC:32248]"}, {"versioned_ensembl_gene_id":"ENSG00000227861.9","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"NG23,C6orf26","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31829818,"end":31831870,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000156968.8","gene_symbol":"MPV17L","gene_name":"MPV17 mitochondrial inner membrane protein like [Source:HGNC Symbol;Acc:HGNC:26827]","synonyms":"MLPH2,MLPH1,FLJ39599,MPV17L1","biotype":"protein_coding","ncbi_id":"255027","summary":null,"start":15395754,"end":15413268,"strand":1,"description":"MPV17 mitochondrial inner membrane protein like [Source:HGNC Symbol;Acc:HGNC:26827]"}, {"versioned_ensembl_gene_id":"ENSG00000165186.11","gene_symbol":"PTCHD1","gene_name":"patched domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26392]","synonyms":"FLJ30296","biotype":"protein_coding","ncbi_id":"139411","summary":"This gene encodes a membrane protein with a patched domain. The encoded protein is similar to Drosophila proteins which act as receptors for the morphogen sonic hedgehog. Deletions in this gene, which is located on the X chromosome, are associated with intellectual disability and autism (PMID: 21091464, PMID: 20844286). [provided by RefSeq, Aug 2011]","start":23334016,"end":23404372,"strand":1,"description":"patched domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26392]"}, {"versioned_ensembl_gene_id":"ENSG00000280180.1","gene_symbol":"AC023824.7","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":35148636,"end":35154366,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183729.3","gene_symbol":"NPBWR1","gene_name":"neuropeptides B and W receptor 1 [Source:HGNC Symbol;Acc:HGNC:4522]","synonyms":"GPR7","biotype":"protein_coding","ncbi_id":"2831","summary":null,"start":52938431,"end":52941117,"strand":1,"description":"neuropeptides B and W receptor 1 [Source:HGNC Symbol;Acc:HGNC:4522]"}, {"versioned_ensembl_gene_id":"ENSG00000257769.1","gene_symbol":"AC026401.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15608474,"end":15610563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226774.1","gene_symbol":"AC073910.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23351013,"end":23351450,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261130.5","gene_symbol":"AC140504.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":15395754,"end":15515348,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280243.1","gene_symbol":"MTCO1P1","gene_name":"mitochondrially encoded cytochrome c oxidase I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7420]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"56167","summary":null,"start":8845566,"end":8846646,"strand":1,"description":"mitochondrially encoded cytochrome c oxidase I pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:7420]"}, {"versioned_ensembl_gene_id":"ENSG00000100206.9","gene_symbol":"DMC1","gene_name":"DNA meiotic recombinase 1 [Source:HGNC Symbol;Acc:HGNC:2927]","synonyms":"LIM15","biotype":"protein_coding","ncbi_id":"11144","summary":"This gene encodes a member of the superfamily of recombinases (also called DNA strand-exchange proteins). Recombinases are important for repairing double-strand DNA breaks during mitosis and meiosis. This protein, which is evolutionarily conserved, is reported to be essential for meiotic homologous recombination and may thus play an important role in generating diversity of genetic information. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]","start":38518949,"end":38570286,"strand":-1,"description":"DNA meiotic recombinase 1 [Source:HGNC Symbol;Acc:HGNC:2927]"}, {"versioned_ensembl_gene_id":"ENSG00000278931.1","gene_symbol":"CR381670.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8857260,"end":8880976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000166783.21","gene_symbol":"MARF1","gene_name":"meiosis regulator and mRNA stability factor 1 [Source:HGNC Symbol;Acc:HGNC:29562]","synonyms":"LMKB,LKAP,KIAA0430,PPP1R34,Marf1","biotype":"protein_coding","ncbi_id":"9665","summary":"This gene encodes a putative peroxisomal protein that appears to be conserved across Euteleostomi. In humans, it may be autoantigenic. [provided by RefSeq, Jul 2010]","start":15594386,"end":15643166,"strand":-1,"description":"meiosis regulator and mRNA stability factor 1 [Source:HGNC Symbol;Acc:HGNC:29562]"}, {"versioned_ensembl_gene_id":"ENSG00000147059.8","gene_symbol":"SPIN2A","gene_name":"spindlin family member 2A [Source:HGNC Symbol;Acc:HGNC:20694]","synonyms":"TDRD25,SPIN2,DXF34","biotype":"protein_coding","ncbi_id":"54466","summary":"This gene encodes one of three members of the DXF34 gene family, located in a 100-kb region of chromosome Xp11.21. [provided by RefSeq, Nov 2009]","start":57134530,"end":57137625,"strand":-1,"description":"spindlin family member 2A [Source:HGNC Symbol;Acc:HGNC:20694]"}, {"versioned_ensembl_gene_id":"ENSG00000163009.8","gene_symbol":"C2orf48","gene_name":"chromosome 2 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:26322]","synonyms":"FLJ25102","biotype":"lincRNA","ncbi_id":"348738","summary":null,"start":10141382,"end":10211725,"strand":1,"description":"chromosome 2 open reading frame 48 [Source:HGNC Symbol;Acc:HGNC:26322]"}, {"versioned_ensembl_gene_id":"ENSG00000232977.6","gene_symbol":"LINC00327","gene_name":"long intergenic non-protein coding RNA 327 [Source:HGNC Symbol;Acc:HGNC:42009]","synonyms":"NCRNA00327","biotype":"lincRNA","ncbi_id":"100506697","summary":null,"start":23466571,"end":23487464,"strand":1,"description":"long intergenic non-protein coding RNA 327 [Source:HGNC Symbol;Acc:HGNC:42009]"}, {"versioned_ensembl_gene_id":"ENSG00000243849.1","gene_symbol":"CFAP44-AS1","gene_name":"CFAP44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41113]","synonyms":"WDR52-AS1","biotype":"antisense_RNA","ncbi_id":"100874029","summary":null,"start":113403991,"end":113433992,"strand":1,"description":"CFAP44 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41113]"}, {"versioned_ensembl_gene_id":"ENSG00000284681.1","gene_symbol":"AC007240.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":10122739,"end":10199288,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231964.1","gene_symbol":"AL731567.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":45444570,"end":45453121,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250192.1","gene_symbol":"AC105390.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":57154577,"end":57156452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000171848.14","gene_symbol":"RRM2","gene_name":"ribonucleotide reductase regulatory subunit M2 [Source:HGNC Symbol;Acc:HGNC:10452]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6241","summary":"This gene encodes one of two non-identical subunits for ribonucleotide reductase. This reductase catalyzes the formation of deoxyribonucleotides from ribonucleotides. Synthesis of the encoded protein (M2) is regulated in a cell-cycle dependent fashion. Transcription from this gene can initiate from alternative promoters, which results in two isoforms that differ in the lengths of their N-termini. Related pseudogenes have been identified on chromosomes 1 and X. [provided by RefSeq, Sep 2009]","start":10120698,"end":10131419,"strand":1,"description":"ribonucleotide reductase regulatory subunit M2 [Source:HGNC Symbol;Acc:HGNC:10452]"}, {"versioned_ensembl_gene_id":"ENSG00000042445.13","gene_symbol":"RETSAT","gene_name":"retinol saturase [Source:HGNC Symbol;Acc:HGNC:25991]","synonyms":"FLJ20296","biotype":"protein_coding","ncbi_id":"54884","summary":null,"start":85342088,"end":85354620,"strand":-1,"description":"retinol saturase [Source:HGNC Symbol;Acc:HGNC:25991]"}, {"versioned_ensembl_gene_id":"ENSG00000227893.1","gene_symbol":"LINC00352","gene_name":"long intergenic non-protein coding RNA 352 [Source:HGNC Symbol;Acc:HGNC:42670]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874138","summary":null,"start":23498796,"end":23502874,"strand":1,"description":"long intergenic non-protein coding RNA 352 [Source:HGNC Symbol;Acc:HGNC:42670]"}, {"versioned_ensembl_gene_id":"ENSG00000012779.10","gene_symbol":"ALOX5","gene_name":"arachidonate 5-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:435]","synonyms":"5-LOX","biotype":"protein_coding","ncbi_id":"240","summary":"This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]","start":45374176,"end":45446119,"strand":1,"description":"arachidonate 5-lipoxygenase [Source:HGNC Symbol;Acc:HGNC:435]"}, {"versioned_ensembl_gene_id":"ENSG00000163453.11","gene_symbol":"IGFBP7","gene_name":"insulin like growth factor binding protein 7 [Source:HGNC Symbol;Acc:HGNC:5476]","synonyms":"PSF,MAC25,IGFBP-7,FSTL2","biotype":"protein_coding","ncbi_id":"3490","summary":"This gene encodes a member of the insulin-like growth factor (IGF)-binding protein (IGFBP) family. IGFBPs bind IGFs with high affinity, and regulate IGF availability in body fluids and tissues and modulate IGF binding to its receptors. This protein binds IGF-I and IGF-II with relatively low affinity, and belongs to a subfamily of low-affinity IGFBPs. It also stimulates prostacyclin production and cell adhesion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and one variant has been associated with retinal arterial macroaneurysm (PMID:21835307). [provided by RefSeq, Dec 2011]","start":57030773,"end":57110385,"strand":-1,"description":"insulin like growth factor binding protein 7 [Source:HGNC Symbol;Acc:HGNC:5476]"}, {"versioned_ensembl_gene_id":"ENSG00000267800.1","gene_symbol":"AC012254.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47137018,"end":47137290,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279894.1","gene_symbol":"Z73965.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":103596608,"end":103598904,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267444.1","gene_symbol":"SMUG1P1","gene_name":"single-strand-selective monofunctional uracil-DNA glycosylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49401]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129143","summary":null,"start":49650350,"end":49651160,"strand":1,"description":"single-strand-selective monofunctional uracil-DNA glycosylase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:49401]"}, {"versioned_ensembl_gene_id":"ENSG00000267674.1","gene_symbol":"AC090227.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49739823,"end":49742063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227556.1","gene_symbol":"AC096531.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":78317157,"end":78317263,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228977.1","gene_symbol":"OR2W1","gene_name":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]","synonyms":"hs6M1-15","biotype":"protein_coding","ncbi_id":"26692","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29044362,"end":29045389,"strand":-1,"description":"olfactory receptor family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:8281]"}, {"versioned_ensembl_gene_id":"ENSG00000228348.1","gene_symbol":"EFCAB14P1","gene_name":"EF-hand calcium binding domain 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44648]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106479047","summary":null,"start":35122022,"end":35122484,"strand":1,"description":"EF-hand calcium binding domain 14 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44648]"}, {"versioned_ensembl_gene_id":"ENSG00000167220.11","gene_symbol":"HDHD2","gene_name":"haloacid dehalogenase like hydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25364]","synonyms":"DKFZP564D1378","biotype":"protein_coding","ncbi_id":"84064","summary":null,"start":47107403,"end":47150520,"strand":-1,"description":"haloacid dehalogenase like hydrolase domain containing 2 [Source:HGNC Symbol;Acc:HGNC:25364]"}, {"versioned_ensembl_gene_id":"ENSG00000284640.1","gene_symbol":"AL590434.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35141515,"end":35146435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000137393.9","gene_symbol":"RNF144B","gene_name":"ring finger protein 144B [Source:HGNC Symbol;Acc:HGNC:21578]","synonyms":"P53RFP,IBRDC2,bA528A10.3","biotype":"protein_coding","ncbi_id":"255488","summary":null,"start":18387350,"end":18468874,"strand":1,"description":"ring finger protein 144B [Source:HGNC Symbol;Acc:HGNC:21578]"}, {"versioned_ensembl_gene_id":"ENSG00000118997.13","gene_symbol":"DNAH7","gene_name":"dynein axonemal heavy chain 7 [Source:HGNC Symbol;Acc:HGNC:18661]","synonyms":"KIAA0944","biotype":"protein_coding","ncbi_id":"56171","summary":"DNAH7 is a component of the inner dynein arm of ciliary axonemes (Zhang et al., 2002 [PubMed 11877439]).[supplied by OMIM, Mar 2008]","start":195737703,"end":196068812,"strand":-1,"description":"dynein axonemal heavy chain 7 [Source:HGNC Symbol;Acc:HGNC:18661]"}, {"versioned_ensembl_gene_id":"ENSG00000158806.13","gene_symbol":"NPM2","gene_name":"nucleophosmin/nucleoplasmin 2 [Source:HGNC Symbol;Acc:HGNC:7930]","synonyms":null,"biotype":"protein_coding","ncbi_id":"10361","summary":null,"start":22024125,"end":22036897,"strand":1,"description":"nucleophosmin/nucleoplasmin 2 [Source:HGNC Symbol;Acc:HGNC:7930]"}, {"versioned_ensembl_gene_id":"ENSG00000206557.5","gene_symbol":"TRIM71","gene_name":"tripartite motif containing 71 [Source:HGNC Symbol;Acc:HGNC:32669]","synonyms":"LIN41,LIN-41","biotype":"protein_coding","ncbi_id":"131405","summary":"The protein encoded by this gene is an E3 ubiquitin-protein ligase that binds with miRNAs and maintains the growth and upkeep of embryonic stem cells. This gene also is involved in the G1-S phase transition of the cell cycle. [provided by RefSeq, Dec 2015]","start":32818018,"end":32897826,"strand":1,"description":"tripartite motif containing 71 [Source:HGNC Symbol;Acc:HGNC:32669]"}, {"versioned_ensembl_gene_id":"ENSG00000239627.3","gene_symbol":"RPL12P20","gene_name":"ribosomal protein L12 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100270923","summary":null,"start":41389115,"end":41389593,"strand":1,"description":"ribosomal protein L12 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36968]"}, {"versioned_ensembl_gene_id":"ENSG00000196507.10","gene_symbol":"TCEAL3","gene_name":"transcription elongation factor A like 3 [Source:HGNC Symbol;Acc:HGNC:28247]","synonyms":"WEX8,MGC15737","biotype":"protein_coding","ncbi_id":"85012","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]","start":103607451,"end":103629690,"strand":1,"description":"transcription elongation factor A like 3 [Source:HGNC Symbol;Acc:HGNC:28247]"}, {"versioned_ensembl_gene_id":"ENSG00000112333.11","gene_symbol":"NR2E1","gene_name":"nuclear receptor subfamily 2 group E member 1 [Source:HGNC Symbol;Acc:HGNC:7973]","synonyms":"XTLL,TLX,TLL","biotype":"protein_coding","ncbi_id":"7101","summary":"The protein encoded by this gene is an orphan receptor involved in retinal development. The encoded protein also regulates adult neural stem cell proliferation and may be involved in control of aggressive behavior. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]","start":108166058,"end":108188809,"strand":1,"description":"nuclear receptor subfamily 2 group E member 1 [Source:HGNC Symbol;Acc:HGNC:7973]"}, {"versioned_ensembl_gene_id":"ENSG00000228635.1","gene_symbol":"CR933783.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29071973,"end":29072748,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259287.2","gene_symbol":"AC010809.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":33858602,"end":33864825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000067840.12","gene_symbol":"PDZD4","gene_name":"PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21167]","synonyms":"PDZRN4L,PDZK4,LU1,LNX5,KIAA1444,FLJ34125","biotype":"protein_coding","ncbi_id":"57595","summary":null,"start":153802166,"end":153830565,"strand":-1,"description":"PDZ domain containing 4 [Source:HGNC Symbol;Acc:HGNC:21167]"}, {"versioned_ensembl_gene_id":"ENSG00000238070.1","gene_symbol":"CR933783.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":29076722,"end":29077317,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224031.1","gene_symbol":"TCEAL3-AS1","gene_name":"TCEAL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41191]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874119","summary":null,"start":103626076,"end":103626492,"strand":-1,"description":"TCEAL3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41191]"}, {"versioned_ensembl_gene_id":"ENSG00000277042.2","gene_symbol":"LYZL6","gene_name":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]","synonyms":"TKAL754,PRO1485,LYC1","biotype":"protein_coding","ncbi_id":"57151","summary":"This gene encodes a member of the C-type lysozyme/alpha-lactalbumin family. C-type lysozymes are bacteriolytic factors that play a role in host defense, whereas alpha-lactalbumins mediate lactose biosynthesis. The encoded protein contains catalytic residues characteristic of C-type lysozymes and may play a role in male reproduction. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jan 2011]","start":35934518,"end":35943699,"strand":-1,"description":"lysozyme like 6 [Source:HGNC Symbol;Acc:HGNC:29614]"}, {"versioned_ensembl_gene_id":"ENSG00000172465.13","gene_symbol":"TCEAL1","gene_name":"transcription elongation factor A like 1 [Source:HGNC Symbol;Acc:HGNC:11616]","synonyms":"WEX9,SIIR,pp21,p21","biotype":"protein_coding","ncbi_id":"9338","summary":"This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. The encoded protein is similar to transcription elongation factor A/transcription factor SII and contains a zinc finger-like motif as well as a sequence related to the transcription factor SII Pol II-binding region. It may exert its effects via protein-protein interactions with other transcriptional regulators rather than via direct binding of DNA. Multiple family members are located on the X chromosome. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]","start":103628704,"end":103630953,"strand":1,"description":"transcription elongation factor A like 1 [Source:HGNC Symbol;Acc:HGNC:11616]"}, {"versioned_ensembl_gene_id":"ENSG00000047315.15","gene_symbol":"POLR2B","gene_name":"RNA polymerase II subunit B [Source:HGNC Symbol;Acc:HGNC:9188]","synonyms":"RPB2","biotype":"protein_coding","ncbi_id":"5431","summary":"This gene encodes the second largest subunit of RNA polymerase II (Pol II), a DNA-dependent RNA polymerase that catalyzes the transcription of DNA into precursors of mRNA, snRNA and microRNA. This subunit and the largest subunit form opposite sides of the center cleft of Pol II. Deletion of the flap loop region of this subunit results in a decrease in the rate of transcriptional elongation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":56977722,"end":57031168,"strand":1,"description":"RNA polymerase II subunit B [Source:HGNC Symbol;Acc:HGNC:9188]"}, {"versioned_ensembl_gene_id":"ENSG00000278224.5","gene_symbol":"PRICKLE4","gene_name":"prickle planar cell polarity protein 4 [Source:HGNC Symbol;Acc:HGNC:16805]","synonyms":"DKFZp761H221,C6orf49,OEBT","biotype":"protein_coding","ncbi_id":"29964","summary":"C6ORF49 is a member of the LIM domain protein family (Teufel et al., 2005 [PubMed 15702247]).[supplied by OMIM, Mar 2008]","start":41780762,"end":41787372,"strand":1,"description":"prickle planar cell polarity protein 4 [Source:HGNC Symbol;Acc:HGNC:16805]"}, {"versioned_ensembl_gene_id":"ENSG00000233687.3","gene_symbol":"OR2B3","gene_name":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]","synonyms":"OR2B3P,OR6-4","biotype":"protein_coding","ncbi_id":"442184","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29086444,"end":29087450,"strand":-1,"description":"olfactory receptor family 2 subfamily B member 3 [Source:HGNC Symbol;Acc:HGNC:8238]"}, {"versioned_ensembl_gene_id":"ENSG00000277206.1","gene_symbol":"AC073349.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":64768156,"end":64769101,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224172.1","gene_symbol":"AC091799.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64735933,"end":64736743,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198838.13","gene_symbol":"RYR3","gene_name":"ryanodine receptor 3 [Source:HGNC Symbol;Acc:HGNC:10485]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6263","summary":"The protein encoded by this gene is a ryanodine receptor, which functions to release calcium from intracellular storage for use in many cellular processes. For example, the encoded protein is involved in skeletal muscle contraction by releasing calcium from the sarcoplasmic reticulum followed by depolarization of T-tubules. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","start":33310945,"end":33866121,"strand":1,"description":"ryanodine receptor 3 [Source:HGNC Symbol;Acc:HGNC:10485]"}, {"versioned_ensembl_gene_id":"ENSG00000197008.9","gene_symbol":"ZNF138","gene_name":"zinc finger protein 138 [Source:HGNC Symbol;Acc:HGNC:12922]","synonyms":"pHZ-32","biotype":"protein_coding","ncbi_id":"7697","summary":null,"start":64794388,"end":64833681,"strand":1,"description":"zinc finger protein 138 [Source:HGNC Symbol;Acc:HGNC:12922]"}, {"versioned_ensembl_gene_id":"ENSG00000224733.1","gene_symbol":"AL034349.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128500527,"end":128501176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225819.1","gene_symbol":"AC013269.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130515997,"end":130526691,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227945.1","gene_symbol":"AL590006.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128027886,"end":128085248,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152093.7","gene_symbol":"CFC1B","gene_name":"cripto, FRL-1, cryptic family 1B [Source:HGNC Symbol;Acc:HGNC:33983]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653275","summary":null,"start":130521197,"end":130528604,"strand":1,"description":"cripto, FRL-1, cryptic family 1B [Source:HGNC Symbol;Acc:HGNC:33983]"}, {"versioned_ensembl_gene_id":"ENSG00000215414.4","gene_symbol":"PSMA6P1","gene_name":"proteasome subunit alpha 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17460]","synonyms":"PSMA6-LIKE,PSMA6Y,PSMA6P","biotype":"processed_pseudogene","ncbi_id":"64596","summary":null,"start":13286638,"end":13287378,"strand":1,"description":"proteasome subunit alpha 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:17460]"}, {"versioned_ensembl_gene_id":"ENSG00000171596.6","gene_symbol":"NMUR1","gene_name":"neuromedin U receptor 1 [Source:HGNC Symbol;Acc:HGNC:4518]","synonyms":"NMU1R,GPR66,GPC-R,FM-3","biotype":"protein_coding","ncbi_id":"10316","summary":null,"start":231523160,"end":231530495,"strand":-1,"description":"neuromedin U receptor 1 [Source:HGNC Symbol;Acc:HGNC:4518]"}, {"versioned_ensembl_gene_id":"ENSG00000127863.15","gene_symbol":"TNFRSF19","gene_name":"TNF receptor superfamily member 19 [Source:HGNC Symbol;Acc:HGNC:11915]","synonyms":"TROY,TRADE,TAJ-alpha,TAJ","biotype":"protein_coding","ncbi_id":"55504","summary":"The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is highly expressed during embryonic development. It has been shown to interact with TRAF family members, and to activate JNK signaling pathway when overexpressed in cells. This receptor is capable of inducing apoptosis by a caspase-independent mechanism, and it is thought to play an essential role in embryonic development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":23570370,"end":23676104,"strand":1,"description":"TNF receptor superfamily member 19 [Source:HGNC Symbol;Acc:HGNC:11915]"}, {"versioned_ensembl_gene_id":"ENSG00000198521.11","gene_symbol":"ZNF43","gene_name":"zinc finger protein 43 [Source:HGNC Symbol;Acc:HGNC:13109]","synonyms":"ZNF39L1,KOX27,HTF6","biotype":"protein_coding","ncbi_id":"7594","summary":"This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008]","start":21804949,"end":21852125,"strand":-1,"description":"zinc finger protein 43 [Source:HGNC Symbol;Acc:HGNC:13109]"}, {"versioned_ensembl_gene_id":"ENSG00000248525.2","gene_symbol":"AC026787.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":9621377,"end":9658458,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262140.1","gene_symbol":"AC010653.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":71833787,"end":71835932,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249781.6","gene_symbol":"LINC02112","gene_name":"long intergenic non-protein coding RNA 2112 [Source:HGNC Symbol;Acc:HGNC:27756]","synonyms":null,"biotype":"lincRNA","ncbi_id":"285692","summary":null,"start":9641305,"end":9903826,"strand":-1,"description":"long intergenic non-protein coding RNA 2112 [Source:HGNC Symbol;Acc:HGNC:27756]"}, {"versioned_ensembl_gene_id":"ENSG00000261438.1","gene_symbol":"AL157394.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":89015836,"end":89017059,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232311.1","gene_symbol":"AL512303.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109826522,"end":109828785,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233292.1","gene_symbol":"AL513533.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":89139044,"end":89139458,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183813.6","gene_symbol":"CCR4","gene_name":"C-C motif chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:1605]","synonyms":"k5-5,CMKBR4,CKR4,ChemR13,CD194,CC-CKR-4","biotype":"protein_coding","ncbi_id":"1233","summary":"The protein encoded by this gene belongs to the G-protein-coupled receptor family . It is a receptor for the CC chemokine - MIP-1, RANTES, TARC and MCP-1. Chemokines are a group of small polypeptide, structurally related molecules that regulate cell trafficking of various types of leukocytes. The chemokines also play fundamental roles in the development, homeostasis, and function of the immune system, and they have effects on cells of the central nervous system as well as on endothelial cells involved in angiogenesis or angiostasis. [provided by RefSeq, Jul 2008]","start":32951574,"end":32956349,"strand":1,"description":"C-C motif chemokine receptor 4 [Source:HGNC Symbol;Acc:HGNC:1605]"}, {"versioned_ensembl_gene_id":"ENSG00000231494.1","gene_symbol":"AC104634.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":231559903,"end":231560364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000146360.8","gene_symbol":"GPR6","gene_name":"G protein-coupled receptor 6 [Source:HGNC Symbol;Acc:HGNC:4515]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2830","summary":null,"start":109978256,"end":109980718,"strand":1,"description":"G protein-coupled receptor 6 [Source:HGNC Symbol;Acc:HGNC:4515]"}, {"versioned_ensembl_gene_id":"ENSG00000283408.1","gene_symbol":"MIR548A1HG","gene_name":"MIR548A1 host gene [Source:HGNC Symbol;Acc:HGNC:53539]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374956","summary":null,"start":18522739,"end":18674001,"strand":1,"description":"MIR548A1 host gene [Source:HGNC Symbol;Acc:HGNC:53539]"}, {"versioned_ensembl_gene_id":"ENSG00000169777.6","gene_symbol":"TAS2R1","gene_name":"taste 2 receptor member 1 [Source:HGNC Symbol;Acc:HGNC:14909]","synonyms":"TRB7,T2R1","biotype":"protein_coding","ncbi_id":"50834","summary":"This gene encodes a member of a family of candidate taste receptors that are members of the G protein-coupled receptor superfamily and that are specifically expressed by taste receptor cells of the tongue and palate epithelia. This intronless taste receptor gene encodes a 7-transmembrane receptor protein, functioning as a bitter taste receptor. This gene is mapped to chromosome 5p15, the location of a genetic locus (PROP) that controls the detection of the bitter compound 6-n-propyl-2-thiouracil. [provided by RefSeq, Jul 2008]","start":9628997,"end":9712378,"strand":-1,"description":"taste 2 receptor member 1 [Source:HGNC Symbol;Acc:HGNC:14909]"}, {"versioned_ensembl_gene_id":"ENSG00000183878.15","gene_symbol":"UTY","gene_name":"ubiquitously transcribed tetratricopeptide repeat containing, Y-linked [Source:HGNC Symbol;Acc:HGNC:12638]","synonyms":"KDM6C,KDM6AL","biotype":"protein_coding","ncbi_id":"7404","summary":"This gene encodes a protein containing tetratricopeptide repeats which are thought to be involved in protein-protein interactions. The encoded protein is also a minor histocompatibility antigen which may induce graft rejection of male stem cell grafts. A large number of alternatively spliced transcripts have been observed for this gene, but the full length nature of some of these variants has not been determined. [provided by RefSeq, Apr 2012]","start":13248379,"end":13480673,"strand":-1,"description":"ubiquitously transcribed tetratricopeptide repeat containing, Y-linked [Source:HGNC Symbol;Acc:HGNC:12638]"}, {"versioned_ensembl_gene_id":"ENSG00000206395.8","gene_symbol":"DDAH2","gene_name":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]","synonyms":"G6A","biotype":"protein_coding","ncbi_id":"23564","summary":"This gene encodes a dimethylarginine dimethylaminohydrolase. The encoded enzyme functions in nitric oxide generation by regulating the cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. The protein may be localized to the mitochondria. Alternative splicing resulting in multiple transcript variants. [provided by RefSeq, Dec 2014]","start":31717256,"end":31720835,"strand":-1,"description":"dimethylarginine dimethylaminohydrolase 2 [Source:HGNC Symbol;Acc:HGNC:2716]"}, {"versioned_ensembl_gene_id":"ENSG00000226931.2","gene_symbol":"OR2J1","gene_name":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]","synonyms":"hs6M1-4,OR6-5,dJ80I19.2,OR2J1P","biotype":"protein_coding","ncbi_id":"442185","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29100753,"end":29102025,"strand":1,"description":"olfactory receptor family 2 subfamily J member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8259]"}, {"versioned_ensembl_gene_id":"ENSG00000254190.1","gene_symbol":"AC023632.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94590115,"end":94590259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000235765.1","gene_symbol":"SAPCD1-AS1","gene_name":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]","synonyms":"C6orf26-AS1","biotype":"processed_transcript","ncbi_id":"104413891","summary":null,"start":31840606,"end":31841884,"strand":-1,"description":"SAPCD1 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:39824]"}, {"versioned_ensembl_gene_id":"ENSG00000250814.1","gene_symbol":"LINC02221","gene_name":"long intergenic non-protein coding RNA 2221 [Source:HGNC Symbol;Acc:HGNC:53090]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105374648","summary":null,"start":9854377,"end":9889937,"strand":1,"description":"long intergenic non-protein coding RNA 2221 [Source:HGNC Symbol;Acc:HGNC:53090]"}, {"versioned_ensembl_gene_id":"ENSG00000254283.1","gene_symbol":"AC023632.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94594411,"end":94594601,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000234951.9","gene_symbol":"SAPCD1","gene_name":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]","synonyms":"C6orf26,NG23","biotype":"protein_coding","ncbi_id":"401251","summary":null,"start":31839095,"end":31841147,"strand":1,"description":"suppressor APC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:13938]"}, {"versioned_ensembl_gene_id":"ENSG00000230855.3","gene_symbol":"OR2J3","gene_name":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]","synonyms":"OR6-6","biotype":"protein_coding","ncbi_id":"442186","summary":"This gene encodes a G-protein-coupled receptor (GPCR) that functions as an olfactory receptor. Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell. The protein encoded by this gene responds to cis-3-hexen-1-ol, which is released by wounded plants, including cut grass. This gene is situated in a cluster of similar olfactory-receptor coding genes on chromosome 6. [provided by RefSeq, May 2013]","start":29112037,"end":29112810,"strand":1,"description":"olfactory receptor family 2 subfamily J member 3 [Source:HGNC Symbol;Acc:HGNC:8261]"}, {"versioned_ensembl_gene_id":"ENSG00000261437.1","gene_symbol":"AC108860.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":94637285,"end":94639467,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000217379.2","gene_symbol":"AL589647.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":19143695,"end":19144160,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277200.1","gene_symbol":"AC005696.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2720801,"end":2723947,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261963.3","gene_symbol":"CCDC92B","gene_name":"coiled-coil domain containing 92B [Source:HGNC Symbol;Acc:HGNC:52279]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"101928991","summary":null,"start":2724411,"end":2749504,"strand":-1,"description":"coiled-coil domain containing 92B [Source:HGNC Symbol;Acc:HGNC:52279]"}, {"versioned_ensembl_gene_id":"ENSG00000272920.1","gene_symbol":"hsa-mir-1253","gene_name":"hsa-mir-1253 [Source:miRBase;Acc:MI0006387]","synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2748078,"end":2748182,"strand":1,"description":"hsa-mir-1253 [Source:miRBase;Acc:MI0006387]"}, {"versioned_ensembl_gene_id":"ENSG00000115875.18","gene_symbol":"SRSF7","gene_name":"serine and arginine rich splicing factor 7 [Source:HGNC Symbol;Acc:HGNC:10789]","synonyms":"ZCRB2,ZCCHC20,SFRS7,RBM37,HSSG1,AAG3,9G8","biotype":"protein_coding","ncbi_id":"6432","summary":"The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an N-terminal RNA recognition motif (RRM) for binding RNA and a C-terminal RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]","start":38743599,"end":38751494,"strand":-1,"description":"serine and arginine rich splicing factor 7 [Source:HGNC Symbol;Acc:HGNC:10789]"}, {"versioned_ensembl_gene_id":"ENSG00000140519.12","gene_symbol":"RHCG","gene_name":"Rh family C glycoprotein [Source:HGNC Symbol;Acc:HGNC:18140]","synonyms":"C15orf6,SLC42A3,RHGK,PDRC2","biotype":"protein_coding","ncbi_id":"51458","summary":null,"start":89471398,"end":89496613,"strand":-1,"description":"Rh family C glycoprotein [Source:HGNC Symbol;Acc:HGNC:18140]"}, {"versioned_ensembl_gene_id":"ENSG00000233407.1","gene_symbol":"AL592182.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50206084,"end":50223127,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000196247.11","gene_symbol":"ZNF107","gene_name":"zinc finger protein 107 [Source:HGNC Symbol;Acc:HGNC:12887]","synonyms":"ZNF588,ZFD25,smap-7","biotype":"protein_coding","ncbi_id":"51427","summary":"This gene encodes a protein containing multiple C2H2-type zinc finger regions. Proteins containing zinc fingers may act as transcriptional regulators, but may also have other cellular functions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":64666083,"end":64711582,"strand":1,"description":"zinc finger protein 107 [Source:HGNC Symbol;Acc:HGNC:12887]"}, {"versioned_ensembl_gene_id":"ENSG00000284645.1","gene_symbol":"AL592182.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50252569,"end":50258994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284696.1","gene_symbol":"AL596275.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50229662,"end":50321170,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227314.12","gene_symbol":"MSH5","gene_name":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]","synonyms":"G7","biotype":"protein_coding","ncbi_id":"4439","summary":"This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]","start":31816274,"end":31839440,"strand":1,"description":"mutS homolog 5 [Source:HGNC Symbol;Acc:HGNC:7328]"}, {"versioned_ensembl_gene_id":"ENSG00000250510.7","gene_symbol":"GPR162","gene_name":"G protein-coupled receptor 162 [Source:HGNC Symbol;Acc:HGNC:16693]","synonyms":"GRCA,A-2","biotype":"protein_coding","ncbi_id":"27239","summary":"This gene was identified upon genomic analysis of a gene-dense region at human chromosome 12p13. It appears to be mainly expressed in the brain; however, its function is not known. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":6821545,"end":6829972,"strand":1,"description":"G protein-coupled receptor 162 [Source:HGNC Symbol;Acc:HGNC:16693]"}, {"versioned_ensembl_gene_id":"ENSG00000214999.3","gene_symbol":"AC129492.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":8079482,"end":8081565,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000278046.4","gene_symbol":"LILRA3","gene_name":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]","synonyms":"HM43,HM31,LIR4,CD85e,LIR-4,ILT6","biotype":"protein_coding","ncbi_id":"11026","summary":"This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]","start":54294418,"end":54306726,"strand":-1,"description":"leukocyte immunoglobulin like receptor A3 [Source:HGNC Symbol;Acc:HGNC:6604]"}, {"versioned_ensembl_gene_id":"ENSG00000104320.13","gene_symbol":"NBN","gene_name":"nibrin [Source:HGNC Symbol;Acc:HGNC:7652]","synonyms":"NBS1,NBS,ATV,AT-V2,AT-V1","biotype":"protein_coding","ncbi_id":"4683","summary":"Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. [provided by RefSeq, Jul 2008]","start":89933336,"end":90003228,"strand":-1,"description":"nibrin [Source:HGNC Symbol;Acc:HGNC:7652]"}, {"versioned_ensembl_gene_id":"ENSG00000234080.3","gene_symbol":"AL596275.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50326131,"end":50327007,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267724.1","gene_symbol":"AC012254.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":47105946,"end":47108062,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229316.1","gene_symbol":"HMGB1P45","gene_name":"high mobility group box 1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39277]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129919","summary":null,"start":50398825,"end":50399773,"strand":-1,"description":"high mobility group box 1 pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:39277]"}, {"versioned_ensembl_gene_id":"ENSG00000172785.18","gene_symbol":"CBWD1","gene_name":"COBW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17134]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55871","summary":null,"start":121038,"end":179147,"strand":-1,"description":"COBW domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17134]"}, {"versioned_ensembl_gene_id":"ENSG00000134049.5","gene_symbol":"IER3IP1","gene_name":"immediate early response 3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18550]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51124","summary":"This gene encodes a small protein that is localized to the endoplasmic reticulum (ER) and may play a role in the ER stress response by mediating cell differentiation and apoptosis. Transcription of this gene is regulated by tumor necrosis factor alpha and specificity protein 1 (Sp1). Mutations in this gene may play a role in microcephaly, epilepsy, and diabetes syndrome (MEDS), and a pseudogene of this gene is located on the long arm of chromosome 12. [provided by RefSeq, Dec 2011]","start":47152834,"end":47176374,"strand":-1,"description":"immediate early response 3 interacting protein 1 [Source:HGNC Symbol;Acc:HGNC:18550]"}, {"versioned_ensembl_gene_id":"ENSG00000184844.6","gene_symbol":"CYCSP45","gene_name":"cytochrome c, somatic pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:24419]","synonyms":"HCP45","biotype":"processed_pseudogene","ncbi_id":"352852","summary":null,"start":153841251,"end":153841565,"strand":1,"description":"cytochrome c, somatic pseudogene 45 [Source:HGNC Symbol;Acc:HGNC:24419]"}, {"versioned_ensembl_gene_id":"ENSG00000268438.1","gene_symbol":"BNIP3P27","gene_name":"BCL2 interacting protein 3 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:49707]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421708","summary":null,"start":21826513,"end":21827279,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:49707]"}, {"versioned_ensembl_gene_id":"ENSG00000163145.12","gene_symbol":"C1QTNF7","gene_name":"C1q and TNF related 7 [Source:HGNC Symbol;Acc:HGNC:14342]","synonyms":"CTRP7","biotype":"protein_coding","ncbi_id":"114905","summary":null,"start":15339818,"end":15446166,"strand":1,"description":"C1q and TNF related 7 [Source:HGNC Symbol;Acc:HGNC:14342]"}, {"versioned_ensembl_gene_id":"ENSG00000260340.1","gene_symbol":"LINC02176","gene_name":"long intergenic non-protein coding RNA 2176 [Source:HGNC Symbol;Acc:HGNC:53038]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371379","summary":null,"start":84928353,"end":84939603,"strand":1,"description":"long intergenic non-protein coding RNA 2176 [Source:HGNC Symbol;Acc:HGNC:53038]"}, {"versioned_ensembl_gene_id":"ENSG00000225671.2","gene_symbol":"FCF1P6","gene_name":"FCF1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100422535","summary":null,"start":50405430,"end":50406024,"strand":-1,"description":"FCF1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:44618]"}, {"versioned_ensembl_gene_id":"ENSG00000153786.12","gene_symbol":"ZDHHC7","gene_name":"zinc finger DHHC-type containing 7 [Source:HGNC Symbol;Acc:HGNC:18459]","synonyms":"ZNF370,SERZ1,SERZ-B,FLJ20279,FLJ10792,DHHC7","biotype":"protein_coding","ncbi_id":"55625","summary":null,"start":84974181,"end":85011535,"strand":-1,"description":"zinc finger DHHC-type containing 7 [Source:HGNC Symbol;Acc:HGNC:18459]"}, {"versioned_ensembl_gene_id":"ENSG00000267228.7","gene_symbol":"AC012254.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":47108188,"end":47176345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259780.3","gene_symbol":"AC009065.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2235689,"end":2236913,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000142700.11","gene_symbol":"DMRTA2","gene_name":"DMRT like family A2 [Source:HGNC Symbol;Acc:HGNC:13908]","synonyms":null,"biotype":"protein_coding","ncbi_id":"63950","summary":null,"start":50417550,"end":50423500,"strand":-1,"description":"DMRT like family A2 [Source:HGNC Symbol;Acc:HGNC:13908]"}, {"versioned_ensembl_gene_id":"ENSG00000279398.1","gene_symbol":"AL078596.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108178871,"end":108179317,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000167967.15","gene_symbol":"E4F1","gene_name":"E4F transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3121]","synonyms":"E4F","biotype":"protein_coding","ncbi_id":"1877","summary":"The zinc finger protein encoded by this gene is one of several cellular transcription factors whose DNA-binding activities are regulated through the action of adenovirus E1A. A 50-kDa amino-terminal product is generated from the full-length protein through proteolytic cleavage. The protein is differentially regulated by E1A-induced phosphorylation. The full-length gene product represses transcription from the E4 promoter in the absence of E1A, while the 50-kDa form acts as a transcriptional activator in its presence. Alternative splicing results in multiple transcripts encoding different proteins. [provided by RefSeq, Jan 2014]","start":2223566,"end":2235742,"strand":1,"description":"E4F transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:3121]"}, {"versioned_ensembl_gene_id":"ENSG00000237071.7","gene_symbol":"TRIM27","gene_name":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]","synonyms":"RFP,RNF76","biotype":"protein_coding","ncbi_id":"5987","summary":"This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]","start":28903816,"end":28924807,"strand":-1,"description":"tripartite motif containing 27 [Source:HGNC Symbol;Acc:HGNC:9975]"}, {"versioned_ensembl_gene_id":"ENSG00000271550.1","gene_symbol":"BNIP3P11","gene_name":"BCL2 interacting protein 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49724]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480286","summary":null,"start":64678954,"end":64687393,"strand":-1,"description":"BCL2 interacting protein 3 pseudogene 11 [Source:HGNC Symbol;Acc:HGNC:49724]"}, {"versioned_ensembl_gene_id":"ENSG00000231765.1","gene_symbol":"PPP1R11P2","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16327]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"94298","summary":null,"start":57229034,"end":57229415,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:16327]"}, {"versioned_ensembl_gene_id":"ENSG00000203435.2","gene_symbol":"E2F3P2","gene_name":"E2F transcription factor 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3117]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420003","summary":null,"start":195994259,"end":195995680,"strand":-1,"description":"E2F transcription factor 3 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3117]"}, {"versioned_ensembl_gene_id":"ENSG00000279569.1","gene_symbol":"AC020763.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":70661667,"end":70665836,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227878.2","gene_symbol":"AC114760.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":196063312,"end":196063963,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000132613.14","gene_symbol":"MTSS1L","gene_name":"MTSS1L, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:25094]","synonyms":"LOC92154,ABBA-1,ABBA","biotype":"protein_coding","ncbi_id":"92154","summary":null,"start":70661204,"end":70686066,"strand":-1,"description":"MTSS1L, I-BAR domain containing [Source:HGNC Symbol;Acc:HGNC:25094]"}, {"versioned_ensembl_gene_id":"ENSG00000275404.4","gene_symbol":"LILRA5","gene_name":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]","synonyms":"CD85,LILRB7,ILT11,CD85f,LIR9","biotype":"protein_coding","ncbi_id":"353514","summary":"The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":54314236,"end":54320273,"strand":-1,"description":"leukocyte immunoglobulin like receptor A5 [Source:HGNC Symbol;Acc:HGNC:16309]"}, {"versioned_ensembl_gene_id":"ENSG00000180211.5","gene_symbol":"FO393411.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39958414,"end":39958833,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231325.9","gene_symbol":"LY6G5C","gene_name":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]","synonyms":"G5c,C6orf20,NG33","biotype":"protein_coding","ncbi_id":"80741","summary":"LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]","start":31664094,"end":31671449,"strand":-1,"description":"lymphocyte antigen 6 family member G5C [Source:HGNC Symbol;Acc:HGNC:13932]"}, {"versioned_ensembl_gene_id":"ENSG00000249252.5","gene_symbol":"AC098829.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15004942,"end":15427914,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213470.4","gene_symbol":"AC073594.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53632788,"end":53633151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228698.2","gene_symbol":"CR759834.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29138023,"end":29138959,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233333.2","gene_symbol":"RNFT1P2","gene_name":"ring finger protein, transmembrane 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44388]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132264","summary":null,"start":78170481,"end":78171237,"strand":-1,"description":"ring finger protein, transmembrane 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:44388]"}, {"versioned_ensembl_gene_id":"ENSG00000188162.10","gene_symbol":"OTOG","gene_name":"otogelin [Source:HGNC Symbol;Acc:HGNC:8516]","synonyms":"FLJ46346,OTGN,mlemp","biotype":"protein_coding","ncbi_id":"340990","summary":"The protein encoded by this gene is a component of the acellular membranes of the inner ear. Disruption of the orthologous mouse gene shows that it plays a role in auditory and vestibular functions. It is involved in fibrillar network organization, the anchoring of otoconial membranes and cupulae to the neuroepithelia, and likely in sound stimulation resistance. Mutations in this gene cause autosomal recessive nonsyndromic deafness, type 18B. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]","start":17547373,"end":17647150,"strand":1,"description":"otogelin [Source:HGNC Symbol;Acc:HGNC:8516]"}, {"versioned_ensembl_gene_id":"ENSG00000135390.17","gene_symbol":"ATP5G2","gene_name":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:842]","synonyms":null,"biotype":"protein_coding","ncbi_id":"517","summary":"This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). There are three separate genes which encode subunit c of the proton channel and they specify precursors with different import sequences but identical mature proteins. The protein encoded by this gene is one of three precursors of subunit c. This gene has multiple pseudogenes. [provided by RefSeq, Jan 2018]","start":53632726,"end":53677408,"strand":-1,"description":"ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) [Source:HGNC Symbol;Acc:HGNC:842]"}, {"versioned_ensembl_gene_id":"ENSG00000137449.15","gene_symbol":"CPEB2","gene_name":"cytoplasmic polyadenylation element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132864","summary":"The protein encoded by this gene is highly similar to cytoplasmic polyadenylation element binding protein (CPEB), an mRNA-binding protein that regulates cytoplasmic polyadenylation of mRNA as a trans factor in oogenesis and spermatogenesis. Studies of the similar gene in mice suggested a possible role of this protein in transcriptionally inactive haploid spermatids. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":15002674,"end":15070153,"strand":1,"description":"cytoplasmic polyadenylation element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21745]"}, {"versioned_ensembl_gene_id":"ENSG00000213979.3","gene_symbol":"RPL7AP14","gene_name":"ribosomal protein L7a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:16590]","synonyms":"RPL7AL4,dJ823N20.2","biotype":"processed_pseudogene","ncbi_id":"140756","summary":null,"start":37444733,"end":37445534,"strand":-1,"description":"ribosomal protein L7a pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:16590]"}, {"versioned_ensembl_gene_id":"ENSG00000196231.7","gene_symbol":"OR2J2","gene_name":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]","synonyms":"hs6M1-6,dJ80I19.4,OR6-8","biotype":"protein_coding","ncbi_id":"26707","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29173447,"end":29174718,"strand":1,"description":"olfactory receptor family 2 subfamily J member 2 [Source:HGNC Symbol;Acc:HGNC:8260]"}, {"versioned_ensembl_gene_id":"ENSG00000245573.7","gene_symbol":"BDNF-AS","gene_name":"BDNF antisense RNA [Source:HGNC Symbol;Acc:HGNC:20608]","synonyms":"NCRNA00049,BT2D,BT2C,BT2B,BT2A,BDNFOS,BDNFAS,BDNF-AS1","biotype":"antisense_RNA","ncbi_id":"497258","summary":null,"start":27506838,"end":27698174,"strand":1,"description":"BDNF antisense RNA [Source:HGNC Symbol;Acc:HGNC:20608]"}, {"versioned_ensembl_gene_id":"ENSG00000225341.1","gene_symbol":"AC013269.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130530275,"end":130537182,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231662.1","gene_symbol":"AL357052.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19290319,"end":19321021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279501.1","gene_symbol":"CR392039.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8996496,"end":9018670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122420.9","gene_symbol":"PTGFR","gene_name":"prostaglandin F receptor [Source:HGNC Symbol;Acc:HGNC:9600]","synonyms":"FP","biotype":"protein_coding","ncbi_id":"5737","summary":"The protein encoded by this gene is member of the G-protein coupled receptor family. This protein is a receptor for prostaglandin F2-alpha (PGF2-alpha), which is known to be a potent luteolytic agent, and may also be involved in modulating intraocular pressure and smooth muscle contraction in uterus. Knockout studies in mice suggest that the interaction of PGF2-alpha with this receptor may initiate parturition in ovarian luteal cells and thus induce luteolysis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":78303884,"end":78539749,"strand":1,"description":"prostaglandin F receptor [Source:HGNC Symbol;Acc:HGNC:9600]"}, {"versioned_ensembl_gene_id":"ENSG00000215236.3","gene_symbol":"RPL7P33","gene_name":"ribosomal protein L7 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35937]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"286348","summary":null,"start":15361393,"end":15362134,"strand":1,"description":"ribosomal protein L7 pseudogene 33 [Source:HGNC Symbol;Acc:HGNC:35937]"}, {"versioned_ensembl_gene_id":"ENSG00000122257.18","gene_symbol":"RBBP6","gene_name":"RB binding protein 6, ubiquitin ligase [Source:HGNC Symbol;Acc:HGNC:9889]","synonyms":"SNAMA,PACT,P2P-R","biotype":"protein_coding","ncbi_id":"5930","summary":"The retinoblastoma tumor suppressor (pRB) protein binds with many other proteins. In various human cancers, pRB suppresses cellular proliferation and is inactivated. Cell cycle-dependent phosphorylation regulates the activity of pRB. This gene encodes a protein which binds to underphosphorylated but not phosphorylated pRB. Multiple alternatively spliced transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":24537693,"end":24572863,"strand":1,"description":"RB binding protein 6, ubiquitin ligase [Source:HGNC Symbol;Acc:HGNC:9889]"}, {"versioned_ensembl_gene_id":"ENSG00000224062.4","gene_symbol":"TUBB4BP5","gene_name":"tubulin beta 4B class IVb pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42335]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480747","summary":null,"start":121451541,"end":121451967,"strand":1,"description":"tubulin beta 4B class IVb pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42335]"}, {"versioned_ensembl_gene_id":"ENSG00000217718.1","gene_symbol":"NDUFB4P4","gene_name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45252]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075092","summary":null,"start":25886964,"end":25887206,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:45252]"}, {"versioned_ensembl_gene_id":"ENSG00000255991.2","gene_symbol":"AC121334.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39466442,"end":39467345,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261461.1","gene_symbol":"UBE2MP1","gene_name":"ubiquitin conjugating enzyme E2 M pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32195]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"606551","summary":null,"start":35169692,"end":35170241,"strand":-1,"description":"ubiquitin conjugating enzyme E2 M pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32195]"}, {"versioned_ensembl_gene_id":"ENSG00000279414.1","gene_symbol":"CR392039.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9026821,"end":9027329,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261608.1","gene_symbol":"SLC25A1P4","gene_name":"solute carrier family 25 member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43848]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100132355","summary":null,"start":35173316,"end":35174093,"strand":1,"description":"solute carrier family 25 member 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:43848]"}, {"versioned_ensembl_gene_id":"ENSG00000259173.2","gene_symbol":"AC090515.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58755625,"end":58756247,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280436.1","gene_symbol":"CR392039.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":9053122,"end":9059060,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270273.1","gene_symbol":"AC121334.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":39539581,"end":39539851,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245975.2","gene_symbol":"AC090515.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":58768072,"end":58770974,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000180284.5","gene_symbol":"AL049610.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103651735,"end":103652106,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000205339.9","gene_symbol":"IPO7","gene_name":"importin 7 [Source:HGNC Symbol;Acc:HGNC:9852]","synonyms":"RANBP7,Imp7","biotype":"protein_coding","ncbi_id":"10527","summary":"The importin-alpha/beta complex and the GTPase Ran mediate nuclear import of proteins with a classical nuclear localization signal. The protein encoded by this gene is a member of a class of approximately 20 potential Ran targets that share a sequence motif related to the Ran-binding site of importin-beta. Similar to importin-beta, this protein prevents the activation of Ran's GTPase by RanGAP1 and inhibits nucleotide exchange on RanGTP, and also binds directly to nuclear pore complexes where it competes for binding sites with importin-beta and transportin. This protein has a Ran-dependent transport cycle and it can cross the nuclear envelope rapidly and in both directions. At least four importin beta-like transport receptors, namely importin beta itself, transportin, RanBP5 and RanBP7, directly bind and import ribosomal proteins. [provided by RefSeq, Jul 2008]","start":9384622,"end":9448126,"strand":1,"description":"importin 7 [Source:HGNC Symbol;Acc:HGNC:9852]"}, {"versioned_ensembl_gene_id":"ENSG00000263427.1","gene_symbol":"AC129492.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8056225,"end":8057621,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000173208.3","gene_symbol":"ABCD2","gene_name":"ATP binding cassette subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:66]","synonyms":"ALDL1,ALDRP,ALDR","biotype":"protein_coding","ncbi_id":"225","summary":"The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown; however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis. [provided by RefSeq, Jul 2008]","start":39550033,"end":39619751,"strand":-1,"description":"ATP binding cassette subfamily D member 2 [Source:HGNC Symbol;Acc:HGNC:66]"}, {"versioned_ensembl_gene_id":"ENSG00000274185.4","gene_symbol":"LILRA4","gene_name":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]","synonyms":"ILT7,CD85g","biotype":"protein_coding","ncbi_id":"23547","summary":"This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015]","start":54316049,"end":54346292,"strand":-1,"description":"leukocyte immunoglobulin like receptor A4 [Source:HGNC Symbol;Acc:HGNC:15503]"}, {"versioned_ensembl_gene_id":"ENSG00000123131.12","gene_symbol":"PRDX4","gene_name":"peroxiredoxin 4 [Source:HGNC Symbol;Acc:HGNC:17169]","synonyms":"AOE37-2","biotype":"protein_coding","ncbi_id":"10549","summary":" The protein encoded by this gene is an antioxidant enzyme and belongs to the peroxiredoxin family. The protein is localized to the cytoplasm. Peroxidases of the peroxiredoxin family reduce hydrogen peroxide and alkyl hydroperoxides to water and alcohol with the use of reducing equivalents derived from thiol-containing donor molecules. This protein has been found to play a regulatory role in the activation of the transcription factor NF-kappaB. [provided by RefSeq, Jul 2008]","start":23664262,"end":23686399,"strand":1,"description":"peroxiredoxin 4 [Source:HGNC Symbol;Acc:HGNC:17169]"}, {"versioned_ensembl_gene_id":"ENSG00000165886.4","gene_symbol":"UBTD1","gene_name":"ubiquitin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25683]","synonyms":"FLJ11807","biotype":"protein_coding","ncbi_id":"80019","summary":"The degradation of many proteins is carried out by the ubiquitin pathway in which proteins are targeted for degradation by covalent conjugation of the polypeptide ubiquitin. This gene encodes a protein that belongs to the ubiquitin family of proteins. The encoded protein is thought to regulate E2 ubiquitin conjugating enzymes belonging to the UBE2D family. [provided by RefSeq, Mar 2014]","start":97498868,"end":97571209,"strand":1,"description":"ubiquitin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25683]"}, {"versioned_ensembl_gene_id":"ENSG00000275011.1","gene_symbol":"AC129492.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":8063936,"end":8072533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182149.20","gene_symbol":"IST1","gene_name":"IST1, ESCRT-III associated factor [Source:HGNC Symbol;Acc:HGNC:28977]","synonyms":"KIAA0174","biotype":"protein_coding","ncbi_id":"9798","summary":"This gene encodes a protein with MIT-interacting motifs that interacts with components of endosomal sorting complexes required for transport (ESCRT). ESCRT functions in vesicle budding, such as that which occurs during membrane abscission in cytokinesis. There is a pseudogene for this gene on chromosome 19. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]","start":71845996,"end":71931199,"strand":1,"description":"IST1, ESCRT-III associated factor [Source:HGNC Symbol;Acc:HGNC:28977]"}, {"versioned_ensembl_gene_id":"ENSG00000272103.1","gene_symbol":"AC026741.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":36861736,"end":36862217,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179477.9","gene_symbol":"ALOX12B","gene_name":"arachidonate 12-lipoxygenase, 12R type [Source:HGNC Symbol;Acc:HGNC:430]","synonyms":"12R-LOX","biotype":"protein_coding","ncbi_id":"242","summary":"This gene encodes an enzyme involved in the conversion of arachidonic acid to 12R-hydroxyeicosatetraenoic acid. Mutations in this gene are associated with nonbullous congenital ichthyosiform erythroderma. [provided by RefSeq, Sep 2015]","start":8072636,"end":8087703,"strand":-1,"description":"arachidonate 12-lipoxygenase, 12R type [Source:HGNC Symbol;Acc:HGNC:430]"}, {"versioned_ensembl_gene_id":"ENSG00000184761.7","gene_symbol":"AC013269.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":130539095,"end":130549883,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105072.8","gene_symbol":"C19orf44","gene_name":"chromosome 19 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:26141]","synonyms":"FLJ21742","biotype":"protein_coding","ncbi_id":"84167","summary":null,"start":16496311,"end":16521352,"strand":1,"description":"chromosome 19 open reading frame 44 [Source:HGNC Symbol;Acc:HGNC:26141]"}, {"versioned_ensembl_gene_id":"ENSG00000220379.2","gene_symbol":"CR759834.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29181658,"end":29182593,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233182.1","gene_symbol":"CR759834.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29215392,"end":29216335,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271095.1","gene_symbol":"BNIP3P28","gene_name":"BCL2 interacting protein 3 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49708]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481966","summary":null,"start":21997648,"end":21998840,"strand":1,"description":"BCL2 interacting protein 3 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:49708]"}, {"versioned_ensembl_gene_id":"ENSG00000160321.14","gene_symbol":"ZNF208","gene_name":"zinc finger protein 208 [Source:HGNC Symbol;Acc:HGNC:12999]","synonyms":"ZNF95,PMIDP","biotype":"protein_coding","ncbi_id":"7757","summary":"Zinc finger proteins (ZNFs), such as ZNF208, bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. A conserved protein motif, termed the Kruppel-associated box (KRAB) domain, mediates protein-protein interactions (Eichler et al., 1998 [PubMed 9724325]). See ZNF91 (MIM 603971) for further information on ZNFs.[supplied by OMIM, Aug 2009]","start":21932958,"end":22010949,"strand":-1,"description":"zinc finger protein 208 [Source:HGNC Symbol;Acc:HGNC:12999]"}, {"versioned_ensembl_gene_id":"ENSG00000183292.12","gene_symbol":"TISP43","gene_name":"uncharacterized LOC150527 [Source:NCBI gene;Acc:150527]","synonyms":null,"biotype":"protein_coding","ncbi_id":"150527","summary":null,"start":130570829,"end":130584161,"strand":1,"description":"uncharacterized LOC150527 [Source:NCBI gene;Acc:150527]"}, {"versioned_ensembl_gene_id":"ENSG00000213100.2","gene_symbol":"KRT18P68","gene_name":"keratin 18 pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:48895]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"139060","summary":null,"start":45983365,"end":45984364,"strand":1,"description":"keratin 18 pseudogene 68 [Source:HGNC Symbol;Acc:HGNC:48895]"}, {"versioned_ensembl_gene_id":"ENSG00000214009.2","gene_symbol":"PCNAP3","gene_name":"proliferating cell nuclear antigen pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43736]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"392454","summary":null,"start":46058751,"end":46059528,"strand":-1,"description":"proliferating cell nuclear antigen pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43736]"}, {"versioned_ensembl_gene_id":"ENSG00000268745.1","gene_symbol":"AL365205.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41791410,"end":41791477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000239719.1","gene_symbol":"AC004890.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":149191043,"end":149191223,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000229145.1","gene_symbol":"ACTBP1","gene_name":"actin, beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:134]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"643309","summary":null,"start":46288016,"end":46289128,"strand":-1,"description":"actin, beta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:134]"}, {"versioned_ensembl_gene_id":"ENSG00000164663.14","gene_symbol":"USP49","gene_name":"ubiquitin specific peptidase 49 [Source:HGNC Symbol;Acc:HGNC:20078]","synonyms":"MGC20741","biotype":"protein_coding","ncbi_id":"25862","summary":null,"start":41789896,"end":41895361,"strand":-1,"description":"ubiquitin specific peptidase 49 [Source:HGNC Symbol;Acc:HGNC:20078]"}, {"versioned_ensembl_gene_id":"ENSG00000236751.1","gene_symbol":"LINC01186","gene_name":"long intergenic non-protein coding RNA 1186 [Source:HGNC Symbol;Acc:HGNC:49573]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927574","summary":null,"start":46325924,"end":46327645,"strand":-1,"description":"long intergenic non-protein coding RNA 1186 [Source:HGNC Symbol;Acc:HGNC:49573]"}, {"versioned_ensembl_gene_id":"ENSG00000254934.5","gene_symbol":"LINC00678","gene_name":"long intergenic non-protein coding RNA 678 [Source:HGNC Symbol;Acc:HGNC:44413]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101410541","summary":null,"start":27617626,"end":27634627,"strand":-1,"description":"long intergenic non-protein coding RNA 678 [Source:HGNC Symbol;Acc:HGNC:44413]"}, {"versioned_ensembl_gene_id":"ENSG00000101350.7","gene_symbol":"KIF3B","gene_name":"kinesin family member 3B [Source:HGNC Symbol;Acc:HGNC:6320]","synonyms":"KLP-11,KIAA0359,FLA8","biotype":"protein_coding","ncbi_id":"9371","summary":"The protein encoded by this gene acts as a heterodimer with kinesin family member 3A to aid in chromosome movement during mitosis and meiosis. The encoded protein is a plus end-directed microtubule motor and can interact with the SMC3 subunit of the cohesin complex. In addition, the encoded protein may be involved in the intracellular movement of membranous organelles. This protein and kinesin family member 3A form the kinesin II subfamily of the kinesin superfamily. [provided by RefSeq, Jul 2008]","start":32277664,"end":32335011,"strand":1,"description":"kinesin family member 3B [Source:HGNC Symbol;Acc:HGNC:6320]"}, {"versioned_ensembl_gene_id":"ENSG00000232408.1","gene_symbol":"AC140481.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":130583549,"end":130590463,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000231235.1","gene_symbol":"AL139811.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46418450,"end":46420079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000220586.1","gene_symbol":"TUBBP9","gene_name":"tubulin beta class I pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42178]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"442210","summary":null,"start":39992815,"end":40000233,"strand":1,"description":"tubulin beta class I pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42178]"}, {"versioned_ensembl_gene_id":"ENSG00000235587.2","gene_symbol":"GAPDHP65","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:4143]","synonyms":"GAPDL10,GAPDHL10","biotype":"processed_pseudogene","ncbi_id":"389849","summary":null,"start":46439709,"end":46440714,"strand":-1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:4143]"}, {"versioned_ensembl_gene_id":"ENSG00000227131.1","gene_symbol":"AL139275.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40271566,"end":40276237,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176697.18","gene_symbol":"BDNF","gene_name":"brain derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:1033]","synonyms":null,"biotype":"protein_coding","ncbi_id":"627","summary":"This gene encodes a member of the nerve growth factor family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Binding of this protein to its cognate receptor promotes neuronal survival in the adult brain. Expression of this gene is reduced in Alzheimer's, Parkinson's, and Huntington's disease patients. This gene may play a role in the regulation of the stress response and in the biology of mood disorders. [provided by RefSeq, Nov 2015]","start":27654893,"end":27722058,"strand":-1,"description":"brain derived neurotrophic factor [Source:HGNC Symbol;Acc:HGNC:1033]"}, {"versioned_ensembl_gene_id":"ENSG00000236380.5","gene_symbol":"VENTXP7","gene_name":"VENT homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:13638]","synonyms":"VENTX1,HPX42","biotype":"processed_pseudogene","ncbi_id":"391518","summary":"Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the Vent homeobox gene family. [provided by RefSeq, Jul 2008]","start":21405737,"end":21406508,"strand":1,"description":"VENT homeobox pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:13638]"}, {"versioned_ensembl_gene_id":"ENSG00000248911.2","gene_symbol":"AC009800.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":52975111,"end":52976116,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000203496.9","gene_symbol":"AL133216.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38453181,"end":38466176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256849.1","gene_symbol":"TCP1P3","gene_name":"t-complex 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21630]","synonyms":"TCP1L3","biotype":"processed_pseudogene","ncbi_id":"400013","summary":null,"start":19941521,"end":19943018,"strand":1,"description":"t-complex 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:21630]"}, {"versioned_ensembl_gene_id":"ENSG00000223770.5","gene_symbol":"AC006145.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":82009177,"end":82029955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228882.1","gene_symbol":"CICP9","gene_name":"capicua transcriptional repressor pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37758]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420293","summary":null,"start":38452987,"end":38455365,"strand":-1,"description":"capicua transcriptional repressor pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:37758]"}, {"versioned_ensembl_gene_id":"ENSG00000255910.1","gene_symbol":"AC024901.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":19775451,"end":20009937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250494.1","gene_symbol":"AC009646.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":53162339,"end":53162987,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188681.11","gene_symbol":"TEKT4P2","gene_name":"tektin 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:40046]","synonyms":"MAFIPL","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100132288","summary":null,"start":9068361,"end":9129752,"strand":-1,"description":"tektin 4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:40046]"}, {"versioned_ensembl_gene_id":"ENSG00000233511.1","gene_symbol":"Z98742.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108252214,"end":108252400,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000083857.13","gene_symbol":"FAT1","gene_name":"FAT atypical cadherin 1 [Source:HGNC Symbol;Acc:HGNC:3595]","synonyms":"CDHF7,FAT,CDHR8","biotype":"protein_coding","ncbi_id":"2195","summary":"This gene is an ortholog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has five epidermal growth factor (EGF)-like repeats and one laminin A-G domain. This gene is expressed at high levels in a number of fetal epithelia. Its product probably functions as an adhesion molecule and/or signaling receptor, and is likely to be important in developmental processes and cell communication. Transcript variants derived from alternative splicing and/or alternative promoter usage exist, but they have not been fully described. [provided by RefSeq, Jul 2008]","start":186587783,"end":186726722,"strand":-1,"description":"FAT atypical cadherin 1 [Source:HGNC Symbol;Acc:HGNC:3595]"}, {"versioned_ensembl_gene_id":"ENSG00000218643.2","gene_symbol":"RPL5P20","gene_name":"ribosomal protein L5 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36660]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100131913","summary":null,"start":19348181,"end":19349076,"strand":1,"description":"ribosomal protein L5 pseudogene 20 [Source:HGNC Symbol;Acc:HGNC:36660]"}, {"versioned_ensembl_gene_id":"ENSG00000147121.15","gene_symbol":"KRBOX4","gene_name":"KRAB box domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26007]","synonyms":"ZNF673,FLJ20344","biotype":"protein_coding","ncbi_id":"55634","summary":"This encodes a zinc finger protein with an N-terminal KRAB (Kruppel-associated) domain found in transcriptional repressors. This gene is located in a region of the X chromosome thought to be involved in nonsyndromic X-linked cognitive disability. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]","start":46446857,"end":46497422,"strand":1,"description":"KRAB box domain containing 4 [Source:HGNC Symbol;Acc:HGNC:26007]"}, {"versioned_ensembl_gene_id":"ENSG00000269615.1","gene_symbol":"MTDHP2","gene_name":"metadherin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52358]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418835","summary":null,"start":21940820,"end":21941533,"strand":1,"description":"metadherin pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:52358]"}, {"versioned_ensembl_gene_id":"ENSG00000279377.1","gene_symbol":"AC003973.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21965708,"end":21968529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000214012.4","gene_symbol":"KRT18P38","gene_name":"keratin 18 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:33407]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"441133","summary":null,"start":19612755,"end":19614036,"strand":1,"description":"keratin 18 pseudogene 38 [Source:HGNC Symbol;Acc:HGNC:33407]"}, {"versioned_ensembl_gene_id":"ENSG00000153956.15","gene_symbol":"CACNA2D1","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 1 [Source:HGNC Symbol;Acc:HGNC:1399]","synonyms":"CACNL2A,CACNA2,MHS3,lncRNA-N3,LINC01112","biotype":"protein_coding","ncbi_id":"781","summary":"The preproprotein encoded by this gene is cleaved into multiple chains that comprise the alpha-2 and delta subunits of the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. Mutations in this gene can cause cardiac deficiencies, including Brugada syndrome and short QT syndrome. Alternate splicing results in multiple transcript variants, some of which may lack the delta subunit portion. [provided by RefSeq, Nov 2014]","start":81946444,"end":82443798,"strand":-1,"description":"calcium voltage-gated channel auxiliary subunit alpha2delta 1 [Source:HGNC Symbol;Acc:HGNC:1399]"}, {"versioned_ensembl_gene_id":"ENSG00000267709.1","gene_symbol":"AC024592.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5847467,"end":5858239,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000140274.13","gene_symbol":"DUOXA2","gene_name":"dual oxidase maturation factor 2 [Source:HGNC Symbol;Acc:HGNC:32698]","synonyms":null,"biotype":"protein_coding","ncbi_id":"405753","summary":"This gene encodes an endoplasmic reticulum protein that is necessary for proper cellular localization and maturation of functional dual oxidase 2. Mutations in this gene have been associated with thyroid dyshormonogenesis 5.[provided by RefSeq, Feb 2010]","start":45114321,"end":45118421,"strand":1,"description":"dual oxidase maturation factor 2 [Source:HGNC Symbol;Acc:HGNC:32698]"}, {"versioned_ensembl_gene_id":"ENSG00000217314.2","gene_symbol":"UQCRFS1P3","gene_name":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39173]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130994","summary":null,"start":19638040,"end":19638808,"strand":-1,"description":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39173]"}, {"versioned_ensembl_gene_id":"ENSG00000140465.13","gene_symbol":"CYP1A1","gene_name":"cytochrome P450 family 1 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2595]","synonyms":"P450DX,P450-C,P1-450,CYP1,CP11","biotype":"protein_coding","ncbi_id":"1543","summary":"This gene, CYP1A1, encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by some polycyclic aromatic hydrocarbons (PAHs), some of which are found in cigarette smoke. The enzyme's endogenous substrate is unknown; however, it is able to metabolize some PAHs to carcinogenic intermediates. The gene has been associated with lung cancer risk. A related family member, CYP1A2, is located approximately 25 kb away from CYP1A1 on chromosome 15. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2016]","start":74719542,"end":74725610,"strand":-1,"description":"cytochrome P450 family 1 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:2595]"}, {"versioned_ensembl_gene_id":"ENSG00000171124.12","gene_symbol":"FUT3","gene_name":"fucosyltransferase 3 (Lewis blood group) [Source:HGNC Symbol;Acc:HGNC:4014]","synonyms":"LE,CD174","biotype":"protein_coding","ncbi_id":"2525","summary":"The Lewis histo-blood group system comprises a set of fucosylated glycosphingolipids that are synthesized by exocrine epithelial cells and circulate in body fluids. The glycosphingolipids function in embryogenesis, tissue differentiation, tumor metastasis, inflammation, and bacterial adhesion. They are secondarily absorbed to red blood cells giving rise to their Lewis phenotype. This gene is a member of the fucosyltransferase family, which catalyzes the addition of fucose to precursor polysaccharides in the last step of Lewis antigen biosynthesis. It encodes an enzyme with alpha(1,3)-fucosyltransferase and alpha(1,4)-fucosyltransferase activities. Mutations in this gene are responsible for the majority of Lewis antigen-negative phenotypes. Differences in the expression of this gene are associated with host susceptibility to viral infection. [provided by RefSeq, Aug 2020]","start":5842888,"end":5851474,"strand":-1,"description":"fucosyltransferase 3 (Lewis blood group) [Source:HGNC Symbol;Acc:HGNC:4014]"}, {"versioned_ensembl_gene_id":"ENSG00000254397.1","gene_symbol":"AC132192.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":9430356,"end":9433486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172201.11","gene_symbol":"ID4","gene_name":"inhibitor of DNA binding 4, HLH protein [Source:HGNC Symbol;Acc:HGNC:5363]","synonyms":"bHLHb27","biotype":"protein_coding","ncbi_id":"3400","summary":"This gene encodes a member of the inhibitor of DNA binding (ID) protein family. The encoded protein lacks DNA binding ability, and instead regulates gene expression through binding to and inhibiting basic helix-loop-helix transcription factors. This protein has been implicated in the regulation of diverse cellular processes that play a role in development and tumorigenesis. [provided by RefSeq, Aug 2017]","start":19837386,"end":19840684,"strand":1,"description":"inhibitor of DNA binding 4, HLH protein [Source:HGNC Symbol;Acc:HGNC:5363]"}, {"versioned_ensembl_gene_id":"ENSG00000279985.1","gene_symbol":"AC008498.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":61114432,"end":61116753,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276945.1","gene_symbol":"AC008498.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":61145846,"end":61146376,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000109445.10","gene_symbol":"ZNF330","gene_name":"zinc finger protein 330 [Source:HGNC Symbol;Acc:HGNC:15462]","synonyms":"NOA36,HSA6591","biotype":"protein_coding","ncbi_id":"27309","summary":null,"start":141220887,"end":141234697,"strand":1,"description":"zinc finger protein 330 [Source:HGNC Symbol;Acc:HGNC:15462]"}, {"versioned_ensembl_gene_id":"ENSG00000279720.1","gene_symbol":"CR392039.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9082601,"end":9083101,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260844.2","gene_symbol":"AC055876.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28763440,"end":28764151,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000198854.5","gene_symbol":"C1orf68","gene_name":"chromosome 1 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:29468]","synonyms":"XP32,LEP7","biotype":"protein_coding","ncbi_id":"100129271","summary":null,"start":152719522,"end":152720470,"strand":1,"description":"chromosome 1 open reading frame 68 [Source:HGNC Symbol;Acc:HGNC:29468]"}, {"versioned_ensembl_gene_id":"ENSG00000112335.14","gene_symbol":"SNX3","gene_name":"sorting nexin 3 [Source:HGNC Symbol;Acc:HGNC:11174]","synonyms":"Grd19","biotype":"protein_coding","ncbi_id":"8724","summary":"This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like most family members. This protein interacts with phosphatidylinositol-3-phosphate, and is involved in protein trafficking. A pseudogene of this gene is present on the sex chromosomes. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":108211222,"end":108261260,"strand":-1,"description":"sorting nexin 3 [Source:HGNC Symbol;Acc:HGNC:11174]"}, {"versioned_ensembl_gene_id":"ENSG00000164182.10","gene_symbol":"NDUFAF2","gene_name":"NADH:ubiquinone oxidoreductase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:28086]","synonyms":"MMTN,NDUFA12L,mimitin,B17.2L","biotype":"protein_coding","ncbi_id":"91942","summary":"NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency. [provided by RefSeq, Jul 2008]","start":60945129,"end":61153037,"strand":1,"description":"NADH:ubiquinone oxidoreductase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:28086]"}, {"versioned_ensembl_gene_id":"ENSG00000110811.19","gene_symbol":"P3H3","gene_name":"prolyl 3-hydroxylase 3 [Source:HGNC Symbol;Acc:HGNC:19318]","synonyms":"LEPREL2,HSU47926,GRCB","biotype":"protein_coding","ncbi_id":"10536","summary":"The protein encoded by this gene belongs to the leprecan family of proteoglycans, which function as collagen prolyl hydroxylases that are required for proper collagen biosynthesis, folding and assembly. This protein, like other family members, is thought to reside in the endoplasmic reticulum. Epigenetic inactivation of this gene is associated with breast and other cancers, suggesting that it may function as a tumor suppressor. [provided by RefSeq, Aug 2013]","start":6828410,"end":6839851,"strand":1,"description":"prolyl 3-hydroxylase 3 [Source:HGNC Symbol;Acc:HGNC:19318]"}, {"versioned_ensembl_gene_id":"ENSG00000214736.7","gene_symbol":"TOMM6","gene_name":"translocase of outer mitochondrial membrane 6 [Source:HGNC Symbol;Acc:HGNC:34528]","synonyms":"Tom6,OBTP","biotype":"protein_coding","ncbi_id":"100188893","summary":null,"start":41787662,"end":41789898,"strand":1,"description":"translocase of outer mitochondrial membrane 6 [Source:HGNC Symbol;Acc:HGNC:34528]"}, {"versioned_ensembl_gene_id":"ENSG00000261367.1","gene_symbol":"AC012645.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30107675,"end":30110541,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275371.1","gene_symbol":"AC012645.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":30110895,"end":30111955,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000102886.14","gene_symbol":"GDPD3","gene_name":"glycerophosphodiester phosphodiesterase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28638]","synonyms":"MGC4171","biotype":"protein_coding","ncbi_id":"79153","summary":null,"start":30104810,"end":30113856,"strand":-1,"description":"glycerophosphodiester phosphodiesterase domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28638]"}, {"versioned_ensembl_gene_id":"ENSG00000228412.7","gene_symbol":"AL022068.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":19324988,"end":19839080,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000172009.14","gene_symbol":"THOP1","gene_name":"thimet oligopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:11793]","synonyms":null,"biotype":"protein_coding","ncbi_id":"7064","summary":"The protein encoded by this gene is a kininase that uses zinc as a cofactor. The encoded oligopeptidase cleaves cytosolic peptides, making them unavailable for display on antigen-presenting cells. This protein also cleaves neuropeptides under 20 aa in length and can degrade beta-amyloid precursor protein to amyloidogenic peptides. [provided by RefSeq, Nov 2015]","start":2785460,"end":2815807,"strand":1,"description":"thimet oligopeptidase 1 [Source:HGNC Symbol;Acc:HGNC:11793]"}, {"versioned_ensembl_gene_id":"ENSG00000257842.5","gene_symbol":"NOVA1-AS1","gene_name":"NOVA1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:19827]","synonyms":"C14orf22","biotype":"antisense_RNA","ncbi_id":"102725045","summary":null,"start":26598412,"end":26806467,"strand":1,"description":"NOVA1 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:19827]"}, {"versioned_ensembl_gene_id":"ENSG00000282525.1","gene_symbol":"AC004675.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":35963502,"end":35965476,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184634.15","gene_symbol":"MED12","gene_name":"mediator complex subunit 12 [Source:HGNC Symbol;Acc:HGNC:11957]","synonyms":"HOPA,FGS1,CAGH45,TRAP230,TNRC11,OPA1,OKS,KIAA0192","biotype":"protein_coding","ncbi_id":"9968","summary":"The initiation of transcription is controlled in part by a large protein assembly known as the preinitiation complex. A component of this preinitiation complex is a 1.2 MDa protein aggregate called Mediator. This Mediator component binds with a CDK8 subcomplex which contains the protein encoded by this gene, mediator complex subunit 12 (MED12), along with MED13, CDK8 kinase, and cyclin C. The CDK8 subcomplex modulates Mediator-polymerase II interactions and thereby regulates transcription initiation and reinitation rates. The MED12 protein is essential for activating CDK8 kinase. Defects in this gene cause X-linked Opitz-Kaveggia syndrome, also known as FG syndrome, and Lujan-Fryns syndrome. [provided by RefSeq, Aug 2009]","start":71118556,"end":71142454,"strand":1,"description":"mediator complex subunit 12 [Source:HGNC Symbol;Acc:HGNC:11957]"}, {"versioned_ensembl_gene_id":"ENSG00000173702.7","gene_symbol":"MUC13","gene_name":"mucin 13, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7511]","synonyms":"DRCC1","biotype":"protein_coding","ncbi_id":"56667","summary":"Epithelial mucins, such as MUC13, are a family of secreted and cell surface glycoproteins expressed by ductal and glandular epithelial tissues (Williams et al., 2001 [PubMed 11278439]).[supplied by OMIM, Jul 2008]","start":124905442,"end":124953819,"strand":-1,"description":"mucin 13, cell surface associated [Source:HGNC Symbol;Acc:HGNC:7511]"}, {"versioned_ensembl_gene_id":"ENSG00000259539.1","gene_symbol":"AC051619.6","gene_name":null,"synonyms":null,"biotype":"3prime_overlapping_ncRNA","ncbi_id":null,"summary":null,"start":45152664,"end":45167526,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257845.1","gene_symbol":"LINC02294","gene_name":"long intergenic non-protein coding RNA 2294 [Source:HGNC Symbol;Acc:HGNC:53210]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927062","summary":null,"start":26775495,"end":26822107,"strand":-1,"description":"long intergenic non-protein coding RNA 2294 [Source:HGNC Symbol;Acc:HGNC:53210]"}, {"versioned_ensembl_gene_id":"ENSG00000140279.12","gene_symbol":"DUOX2","gene_name":"dual oxidase 2 [Source:HGNC Symbol;Acc:HGNC:13273]","synonyms":"THOX2,P138-TOX,P138(TOX),LNOX2","biotype":"protein_coding","ncbi_id":"50506","summary":"The protein encoded by this gene is a glycoprotein and a member of the NADPH oxidase family. The synthesis of thyroid hormone is catalyzed by a protein complex located at the apical membrane of thyroid follicular cells. This complex contains an iodide transporter, thyroperoxidase, and a peroxide generating system that includes this encoded protein and DUOX1. This protein is known as dual oxidase because it has both a peroxidase homology domain and a gp91phox domain. [provided by RefSeq, Jul 2008]","start":45092650,"end":45114344,"strand":-1,"description":"dual oxidase 2 [Source:HGNC Symbol;Acc:HGNC:13273]"}, {"versioned_ensembl_gene_id":"ENSG00000275095.2","gene_symbol":"CCL16","gene_name":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]","synonyms":"LMC,LEC,LCC-1,HCC-4,CKb12,SCYL4,SCYA16,NCC-4,Mtn-1","biotype":"protein_coding","ncbi_id":"6360","summary":"This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for lymphocytes and monocytes but not for neutrophils. This cytokine also shows a potent myelosuppressive activity and suppresses proliferation of myeloid progenitor cells. The expression of this gene is upregulated by IL-10. [provided by RefSeq, Jul 2008]","start":35976525,"end":35981528,"strand":-1,"description":"C-C motif chemokine ligand 16 [Source:HGNC Symbol;Acc:HGNC:10614]"}, {"versioned_ensembl_gene_id":"ENSG00000124593.15","gene_symbol":"AL365205.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":41780349,"end":41790141,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279381.1","gene_symbol":"CR392039.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":9088188,"end":9088391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224633.1","gene_symbol":"CR933842.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":29290867,"end":29291809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257185.1","gene_symbol":"LINC02293","gene_name":"long intergenic non-protein coding RNA 2293 [Source:HGNC Symbol;Acc:HGNC:53209]","synonyms":null,"biotype":"lincRNA","ncbi_id":"102724890","summary":null,"start":26809417,"end":26836458,"strand":1,"description":"long intergenic non-protein coding RNA 2293 [Source:HGNC Symbol;Acc:HGNC:53209]"}, {"versioned_ensembl_gene_id":"ENSG00000265712.1","gene_symbol":"AC027216.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51687525,"end":51688209,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000184575.11","gene_symbol":"XPOT","gene_name":"exportin for tRNA [Source:HGNC Symbol;Acc:HGNC:12826]","synonyms":"XPO3","biotype":"protein_coding","ncbi_id":"11260","summary":"This gene encodes a protein belonging to the RAN-GTPase exportin family that mediates export of tRNA from the nucleus to the cytoplasm. Translocation of tRNA to the cytoplasm occurs once exportin has bound both tRNA and GTP-bound RAN. [provided by RefSeq, Jul 2008]","start":64404350,"end":64451127,"strand":1,"description":"exportin for tRNA [Source:HGNC Symbol;Acc:HGNC:12826]"}, {"versioned_ensembl_gene_id":"ENSG00000137218.10","gene_symbol":"FRS3","gene_name":"fibroblast growth factor receptor substrate 3 [Source:HGNC Symbol;Acc:HGNC:16970]","synonyms":"SNT-2,FRS2beta,FRS2B","biotype":"protein_coding","ncbi_id":"10817","summary":"This gene encodes a substrate for the fibroblast growth factor receptor. The encoded protein is found in the peripheral plasma membrane and links fibroblast growth factor receptor stimulation to activators of Ras. The encoded protein down-regulates extracellular regulated kinase 2 through direct binding. [provided by RefSeq, Jul 2013]","start":41770176,"end":41786542,"strand":-1,"description":"fibroblast growth factor receptor substrate 3 [Source:HGNC Symbol;Acc:HGNC:16970]"}, {"versioned_ensembl_gene_id":"ENSG00000268087.1","gene_symbol":"AC008764.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16610411,"end":16636531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000268309.1","gene_symbol":"AC008764.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16551773,"end":16552328,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000224072.1","gene_symbol":"AL139811.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":46454097,"end":46457199,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000105085.10","gene_symbol":"MED26","gene_name":"mediator complex subunit 26 [Source:HGNC Symbol;Acc:HGNC:2376]","synonyms":"CRSP70,CRSP7","biotype":"protein_coding","ncbi_id":"9441","summary":"The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008]","start":16574907,"end":16629062,"strand":-1,"description":"mediator complex subunit 26 [Source:HGNC Symbol;Acc:HGNC:2376]"}, {"versioned_ensembl_gene_id":"ENSG00000281819.1","gene_symbol":"AC022882.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":56205125,"end":56205625,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117523.15","gene_symbol":"PRRC2C","gene_name":"proline rich coiled-coil 2C [Source:HGNC Symbol;Acc:HGNC:24903]","synonyms":"XTP2,KIAA1096,BAT2L2,BAT2D1","biotype":"protein_coding","ncbi_id":"23215","summary":null,"start":171485551,"end":171593511,"strand":1,"description":"proline rich coiled-coil 2C [Source:HGNC Symbol;Acc:HGNC:24903]"}, {"versioned_ensembl_gene_id":"ENSG00000281853.1","gene_symbol":"AL034349.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128504663,"end":128505312,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280612.1","gene_symbol":"AL590006.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":128032022,"end":128089384,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274446.1","gene_symbol":"AP001005.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":94202,"end":94330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000245067.6","gene_symbol":"IGFBP7-AS1","gene_name":"IGFBP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40296]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"255130","summary":null,"start":57109762,"end":57205510,"strand":1,"description":"IGFBP7 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40296]"}, {"versioned_ensembl_gene_id":"ENSG00000283576.1","gene_symbol":"AC100810.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1726273,"end":1726557,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262752.1","gene_symbol":"AP000705.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22134698,"end":22136083,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000170265.11","gene_symbol":"ZNF282","gene_name":"zinc finger protein 282 [Source:HGNC Symbol;Acc:HGNC:13076]","synonyms":"HUB1","biotype":"protein_coding","ncbi_id":"8427","summary":null,"start":149195485,"end":149226248,"strand":1,"description":"zinc finger protein 282 [Source:HGNC Symbol;Acc:HGNC:13076]"}, {"versioned_ensembl_gene_id":"ENSG00000254265.1","gene_symbol":"AC100810.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":1730206,"end":1731452,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213943.3","gene_symbol":"KRT18P17","gene_name":"keratin 18 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:33385]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"344866","summary":null,"start":12787393,"end":12788671,"strand":-1,"description":"keratin 18 pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:33385]"}, {"versioned_ensembl_gene_id":"ENSG00000261847.1","gene_symbol":"AP000705.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22153950,"end":22154299,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000262476.2","gene_symbol":"AP000705.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22209939,"end":22212813,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000068024.16","gene_symbol":"HDAC4","gene_name":"histone deacetylase 4 [Source:HGNC Symbol;Acc:HGNC:14063]","synonyms":"HA6116,BDMR,KIAA0288,HDACA,HDAC-A,HDAC-4,HD4","biotype":"protein_coding","ncbi_id":"9759","summary":"Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It possesses histone deacetylase activity and represses transcription when tethered to a promoter. This protein does not bind DNA directly, but through transcription factors MEF2C and MEF2D. It seems to interact in a multiprotein complex with RbAp48 and HDAC3. [provided by RefSeq, Jul 2008]","start":239048168,"end":239401654,"strand":-1,"description":"histone deacetylase 4 [Source:HGNC Symbol;Acc:HGNC:14063]"}, {"versioned_ensembl_gene_id":"ENSG00000263006.6","gene_symbol":"ROCK1P1","gene_name":"Rho associated coiled-coil containing protein kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37832]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"727758","summary":null,"start":109065,"end":122219,"strand":1,"description":"Rho associated coiled-coil containing protein kinase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:37832]"}, {"versioned_ensembl_gene_id":"ENSG00000225542.1","gene_symbol":"ZNF385D-AS1","gene_name":"ZNF385D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41136]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874216","summary":null,"start":21542816,"end":21579959,"strand":1,"description":"ZNF385D antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:41136]"}, {"versioned_ensembl_gene_id":"ENSG00000269949.1","gene_symbol":"AC069307.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":56960927,"end":56961373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000084092.6","gene_symbol":"NOA1","gene_name":"nitric oxide associated 1 [Source:HGNC Symbol;Acc:HGNC:28473]","synonyms":"MTG3,MGC3232,hNOA1,hAtNOS1,C4orf14","biotype":"protein_coding","ncbi_id":"84273","summary":"The protein encoded by this gene is a nuclear-encoded GTPase that functions in the mitochondrion. Upon translation, this protein is imported into the nucleus and then into the nucleolus before being exported to the mitochondrion. The encoded protein is required for oxygen-dependent regulation of mitochondrial respiratory complexes and for mitochondrial protein synthesis. [provided by RefSeq, Dec 2015]","start":56963370,"end":56978823,"strand":-1,"description":"nitric oxide associated 1 [Source:HGNC Symbol;Acc:HGNC:28473]"}, {"versioned_ensembl_gene_id":"ENSG00000151789.10","gene_symbol":"ZNF385D","gene_name":"zinc finger protein 385D [Source:HGNC Symbol;Acc:HGNC:26191]","synonyms":"ZNF659,FLJ22419","biotype":"protein_coding","ncbi_id":"79750","summary":null,"start":21412222,"end":22373321,"strand":-1,"description":"zinc finger protein 385D [Source:HGNC Symbol;Acc:HGNC:26191]"}, {"versioned_ensembl_gene_id":"ENSG00000227516.1","gene_symbol":"AL160163.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41868622,"end":41869731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258256.1","gene_symbol":"AC011773.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":85222446,"end":85245717,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260073.2","gene_symbol":"AC023824.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35192687,"end":35195661,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260590.1","gene_symbol":"AC023824.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":35193335,"end":35193734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271536.1","gene_symbol":"AC073046.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":73877566,"end":73878862,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256951.1","gene_symbol":"AC055876.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":28789199,"end":28789486,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261398.1","gene_symbol":"AC023824.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":35195779,"end":35197544,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257807.1","gene_symbol":"AC003686.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47484689,"end":47485722,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138434.16","gene_symbol":"SSFA2","gene_name":"sperm specific antigen 2 [Source:HGNC Symbol;Acc:HGNC:11319]","synonyms":"SPAG13,KRAP,KIAA1927,CS-1","biotype":"protein_coding","ncbi_id":"6744","summary":null,"start":181891833,"end":181930738,"strand":1,"description":"sperm specific antigen 2 [Source:HGNC Symbol;Acc:HGNC:11319]"}, {"versioned_ensembl_gene_id":"ENSG00000271616.1","gene_symbol":"AC055876.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28830619,"end":28831182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263141.5","gene_symbol":"PAXBP1","gene_name":"PAX3 and PAX7 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13579]","synonyms":"C21orf66,GCFC1,GCFC,fSAP105","biotype":"protein_coding","ncbi_id":"94104","summary":"This gene encodes a protein that may bind to GC-rich DNA sequences, which suggests its involvement in the regulation of transcription. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2009]","start":32769814,"end":32771858,"strand":-1,"description":"PAX3 and PAX7 binding protein 1 [Source:HGNC Symbol;Acc:HGNC:13579]"}, {"versioned_ensembl_gene_id":"ENSG00000198952.8","gene_symbol":"SMG5","gene_name":"SMG5, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:24644]","synonyms":"LPTSRP1,LPTS-RP1,KIAA1089,EST1B,SMG-5,RP11-54H19.7","biotype":"protein_coding","ncbi_id":"23381","summary":"SMG5 is involved in nonsense-mediated mRNA decay (Ohnishi et al., 2003 [PubMed 14636577]).[supplied by OMIM, Mar 2008]","start":156249224,"end":156282825,"strand":-1,"description":"SMG5, nonsense mediated mRNA decay factor [Source:HGNC Symbol;Acc:HGNC:24644]"}, {"versioned_ensembl_gene_id":"ENSG00000270301.1","gene_symbol":"AC174071.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":28857882,"end":28858398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000232431.3","gene_symbol":"AC055876.1","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":28788243,"end":28792002,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284632.1","gene_symbol":"AL354702.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38754216,"end":38815979,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279748.1","gene_symbol":"AC008764.9","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16586905,"end":16589409,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269085.1","gene_symbol":"AC008764.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16565551,"end":16566330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261649.6","gene_symbol":"GOLGA6L7P","gene_name":"golgin A6 family-like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:37442]","synonyms":"GOLGA6L7","biotype":"protein_coding","ncbi_id":"728310","summary":null,"start":28841833,"end":28848675,"strand":-1,"description":"golgin A6 family-like 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:37442]"}, {"versioned_ensembl_gene_id":"ENSG00000261752.1","gene_symbol":"AGGF1P8","gene_name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51745]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128804","summary":null,"start":35258630,"end":35259629,"strand":1,"description":"angiogenic factor with G-patch and FHA domains 1 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:51745]"}, {"versioned_ensembl_gene_id":"ENSG00000279529.1","gene_symbol":"AC008764.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":16572624,"end":16575340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000269399.2","gene_symbol":"AC008764.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16542746,"end":16544814,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000257905.1","gene_symbol":"AC004486.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":47593208,"end":47593440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260967.1","gene_symbol":"RARRES2P5","gene_name":"retinoic acid receptor responder 2 pseudogene 5 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000250384.1","gene_symbol":"UBE2CP3","gene_name":"ubiquitin conjugating enzyme E2 C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129983","summary":null,"start":57072683,"end":57073132,"strand":1,"description":"ubiquitin conjugating enzyme E2 C pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43552]"}, {"versioned_ensembl_gene_id":"ENSG00000260984.1","gene_symbol":"FGFR3P5","gene_name":"fibroblast growth factor receptor 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37950]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100420952","summary":null,"start":35232412,"end":35235984,"strand":-1,"description":"fibroblast growth factor receptor 3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:37950]"}, {"versioned_ensembl_gene_id":"ENSG00000261377.5","gene_symbol":"PDCD6IPP2","gene_name":"PDCD6IP pseudogene 2 [Source:HGNC 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[Source:HGNC Symbol;Acc:HGNC:48705]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"105377820","summary":null,"start":35255192,"end":35255633,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:48705]"}, {"versioned_ensembl_gene_id":"ENSG00000225971.1","gene_symbol":"AC003071.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30136673,"end":30137681,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259897.2","gene_symbol":"FRG2JP","gene_name":"FSHD region gene 2 family member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:51796]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101059926","summary":null,"start":35245916,"end":35247534,"strand":-1,"description":"FSHD region gene 2 family member J, pseudogene [Source:HGNC Symbol;Acc:HGNC:51796]"}, {"versioned_ensembl_gene_id":"ENSG00000283361.1","gene_symbol":"AL160396.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":114179238,"end":114223084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279159.1","gene_symbol":"AC003681.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":29978950,"end":30028236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176635.17","gene_symbol":"HORMAD2","gene_name":"HORMA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28383]","synonyms":"MGC26710,CT46.2","biotype":"protein_coding","ncbi_id":"150280","summary":null,"start":30080174,"end":30177075,"strand":1,"description":"HORMA domain containing 2 [Source:HGNC Symbol;Acc:HGNC:28383]"}, {"versioned_ensembl_gene_id":"ENSG00000123496.7","gene_symbol":"IL13RA2","gene_name":"interleukin 13 receptor subunit alpha 2 [Source:HGNC 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This protein binds IL13 with high affinity, but lacks cytoplasmic domain, and does not appear to function as a signal mediator. It is reported to play a role in the internalization of IL13. [provided by RefSeq, Jul 2008]","start":115003975,"end":115019977,"strand":-1,"description":"interleukin 13 receptor subunit alpha 2 [Source:HGNC Symbol;Acc:HGNC:5975]"}, {"versioned_ensembl_gene_id":"ENSG00000259932.1","gene_symbol":"AC051619.7","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45198517,"end":45199139,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260035.1","gene_symbol":"AC051619.8","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":45200325,"end":45200632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000138606.19","gene_symbol":"SHF","gene_name":"Src homology 2 domain containing F [Source:HGNC Symbol;Acc:HGNC:25116]","synonyms":null,"biotype":"protein_coding","ncbi_id":"90525","summary":null,"start":45167214,"end":45201175,"strand":-1,"description":"Src homology 2 domain containing F [Source:HGNC Symbol;Acc:HGNC:25116]"}, {"versioned_ensembl_gene_id":"ENSG00000089234.15","gene_symbol":"BRAP","gene_name":"BRCA1 associated protein [Source:HGNC Symbol;Acc:HGNC:1099]","synonyms":"RNF52,IMP,BRAP2","biotype":"protein_coding","ncbi_id":"8315","summary":"The protein encoded by this gene was identified by its ability to bind to the nuclear localization signal of BRCA1 and other proteins. 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[provided by RefSeq, Jul 2008]","start":111642146,"end":111685986,"strand":-1,"description":"BRCA1 associated protein [Source:HGNC Symbol;Acc:HGNC:1099]"}, {"versioned_ensembl_gene_id":"ENSG00000277692.1","gene_symbol":"AL121583.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32355053,"end":32355734,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236713.1","gene_symbol":"AL356292.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":150780272,"end":150780644,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000249890.1","gene_symbol":"AC107401.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":69021656,"end":69022340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226070.1","gene_symbol":"AL139275.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40358744,"end":40369474,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204091.7","gene_symbol":"TDRG1","gene_name":"testis development related 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43642]","synonyms":"lincRNA-NR_024015,LINC00532","biotype":"antisense_RNA","ncbi_id":"732253","summary":null,"start":40334954,"end":40379887,"strand":1,"description":"testis development related 1 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:43642]"}, {"versioned_ensembl_gene_id":"ENSG00000223351.5","gene_symbol":"ZNF385D-AS2","gene_name":"ZNF385D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42420]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874221","summary":null,"start":21942566,"end":21979828,"strand":1,"description":"ZNF385D antisense RNA 2 [Source:HGNC Symbol;Acc:HGNC:42420]"}, {"versioned_ensembl_gene_id":"ENSG00000180979.9","gene_symbol":"LRRC57","gene_name":"leucine rich repeat containing 57 [Source:HGNC Symbol;Acc:HGNC:26719]","synonyms":"FLJ36812","biotype":"protein_coding","ncbi_id":"255252","summary":null,"start":42537820,"end":42548802,"strand":-1,"description":"leucine rich repeat containing 57 [Source:HGNC Symbol;Acc:HGNC:26719]"}, {"versioned_ensembl_gene_id":"ENSG00000255496.1","gene_symbol":"AC103796.1","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":27696312,"end":27877648,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000177447.6","gene_symbol":"CBX3P1","gene_name":"chromobox 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33950]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"159770","summary":null,"start":27806443,"end":27806996,"strand":1,"description":"chromobox 3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33950]"}, {"versioned_ensembl_gene_id":"ENSG00000226833.5","gene_symbol":"AC092164.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":28708953,"end":28736205,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240036.4","gene_symbol":"AC104563.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27581680,"end":27582055,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261241.6","gene_symbol":"LINC02128","gene_name":"long intergenic non-protein coding RNA 2128 [Source:HGNC Symbol;Acc:HGNC:52986]","synonyms":null,"biotype":"lincRNA","ncbi_id":"107983964","summary":null,"start":50840017,"end":50901063,"strand":1,"description":"long intergenic non-protein coding RNA 2128 [Source:HGNC Symbol;Acc:HGNC:52986]"}, {"versioned_ensembl_gene_id":"ENSG00000279766.1","gene_symbol":"AC067931.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":140572142,"end":140572812,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250919.1","gene_symbol":"UGT2B26P","gene_name":"UDP glucuronosyltransferase family 2 member B26, pseudogene [Source:HGNC Symbol;Acc:HGNC:12550]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"54570","summary":null,"start":69027831,"end":69044578,"strand":1,"description":"UDP glucuronosyltransferase family 2 member B26, pseudogene [Source:HGNC Symbol;Acc:HGNC:12550]"}, {"versioned_ensembl_gene_id":"ENSG00000204092.2","gene_symbol":"LINC00951","gene_name":"long intergenic non-protein coding RNA 951 [Source:HGNC Symbol;Acc:HGNC:48662]","synonyms":"lincRNA-uc003opf.1,FLJ41649","biotype":"lincRNA","ncbi_id":"401260","summary":null,"start":40344344,"end":40346151,"strand":-1,"description":"long intergenic non-protein coding RNA 951 [Source:HGNC Symbol;Acc:HGNC:48662]"}, {"versioned_ensembl_gene_id":"ENSG00000215151.4","gene_symbol":"ABCD1P2","gene_name":"ATP binding cassette subfamily D member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:63]","synonyms":"bA453N3.6","biotype":"unprocessed_pseudogene","ncbi_id":"26983","summary":null,"start":38601418,"end":38605609,"strand":1,"description":"ATP binding cassette subfamily D member 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:63]"}, {"versioned_ensembl_gene_id":"ENSG00000136243.16","gene_symbol":"NUPL2","gene_name":"nucleoporin like 2 [Source:HGNC Symbol;Acc:HGNC:17010]","synonyms":"CG1,NLP_1,H_RG271G13.9,hCG1","biotype":"protein_coding","ncbi_id":"11097","summary":null,"start":23181827,"end":23201011,"strand":1,"description":"nucleoporin like 2 [Source:HGNC Symbol;Acc:HGNC:17010]"}, {"versioned_ensembl_gene_id":"ENSG00000277133.1","gene_symbol":"AL133173.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":38617255,"end":38617344,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000144730.17","gene_symbol":"IL17RD","gene_name":"interleukin 17 receptor D [Source:HGNC Symbol;Acc:HGNC:17616]","synonyms":"SEF,IL17RLM,IL-17RD,FLJ35755","biotype":"protein_coding","ncbi_id":"54756","summary":"This gene encodes a membrane protein belonging to the interleukin-17 receptor (IL-17R) protein family. The encoded protein is a component of the interleukin-17 receptor signaling complex, and the interaction between this protein and IL-17R does not require the interleukin. The gene product also affects fibroblast growth factor signaling, inhibiting or stimulating growth through MAPK/ERK signaling. Alternate splicing generates multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2016]","start":57089982,"end":57170306,"strand":-1,"description":"interleukin 17 receptor D [Source:HGNC Symbol;Acc:HGNC:17616]"}, {"versioned_ensembl_gene_id":"ENSG00000225638.1","gene_symbol":"PABPC1P12","gene_name":"poly(A) binding protein cytoplasmic 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37994]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100129604","summary":null,"start":38635908,"end":38638082,"strand":1,"description":"poly(A) binding protein cytoplasmic 1 pseudogene 12 [Source:HGNC Symbol;Acc:HGNC:37994]"}, {"versioned_ensembl_gene_id":"ENSG00000260042.1","gene_symbol":"AC025810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50856614,"end":50879278,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275594.4","gene_symbol":"ADAM32","gene_name":"ADAM metallopeptidase domain 32 [Source:HGNC Symbol;Acc:HGNC:15479]","synonyms":null,"biotype":"protein_coding","ncbi_id":"203102","summary":"This gene encodes a member of the disintegrin family of membrane-anchored proteins that play a role in diverse biological processes such as brain development, fertilization, tumor development and inflammation. This gene is predominantly expressed in the testis. The encoded protein undergoes proteolytic processing to generate a mature polypeptide comprised of an metalloprotease, disintegrin and epidermal growth factor-like domains. This gene is located in a cluster of other disintegrin and metallopeptidase family genes on chromosome 8. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]","start":39106990,"end":39284943,"strand":1,"description":"ADAM metallopeptidase domain 32 [Source:HGNC Symbol;Acc:HGNC:15479]"}, {"versioned_ensembl_gene_id":"ENSG00000159455.8","gene_symbol":"LCE2B","gene_name":"late cornified envelope 2B [Source:HGNC Symbol;Acc:HGNC:16610]","synonyms":"XP5,SPRL1B,LEP10","biotype":"protein_coding","ncbi_id":"26239","summary":"This gene is one of the at least 20 genes expressed during epidermal differentiation and located on chromosomal band 1q21. This gene is involved in epidermal differentiation, and it is expressed at high levels in normal and psoriatic skin, but not in cultured keratinocytes or in any other tested cell types or tissues. [provided by RefSeq, Jul 2008]","start":152686123,"end":152687401,"strand":1,"description":"late cornified envelope 2B [Source:HGNC Symbol;Acc:HGNC:16610]"}, {"versioned_ensembl_gene_id":"ENSG00000255566.1","gene_symbol":"AC135279.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":64442510,"end":64443330,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000182372.9","gene_symbol":"CLN8","gene_name":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]","synonyms":"FLJ39417,EPMR,C8orf61","biotype":"protein_coding","ncbi_id":"2055","summary":"This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2017]","start":1755778,"end":1801711,"strand":1,"description":"CLN8, transmembrane ER and ERGIC protein [Source:HGNC Symbol;Acc:HGNC:2079]"}, {"versioned_ensembl_gene_id":"ENSG00000226573.1","gene_symbol":"AC003071.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30105094,"end":30105408,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000112459.5","gene_symbol":"OR14J1","gene_name":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]","synonyms":"OR5U1,hs6M1-28","biotype":"protein_coding","ncbi_id":"442191","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29306920,"end":29307885,"strand":1,"description":"olfactory receptor family 14 subfamily J member 1 [Source:HGNC Symbol;Acc:HGNC:13971]"}, {"versioned_ensembl_gene_id":"ENSG00000279977.1","gene_symbol":"AC008764.10","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":16610374,"end":16612203,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227201.2","gene_symbol":"CNN2P1","gene_name":"calponin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39526]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646467","summary":null,"start":30046276,"end":30047193,"strand":-1,"description":"calponin 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39526]"}, {"versioned_ensembl_gene_id":"ENSG00000227117.6","gene_symbol":"HORMAD2-AS1","gene_name":"HORMAD2 and MTMR3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50729]","synonyms":"NONHSAG033653,MTMR3-AS1","biotype":"antisense_RNA","ncbi_id":"101929664","summary":null,"start":30008742,"end":30080480,"strand":-1,"description":"HORMAD2 and MTMR3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50729]"}, {"versioned_ensembl_gene_id":"ENSG00000257476.1","gene_symbol":"LINC02459","gene_name":"long intergenic non-protein coding RNA 2459 [Source:HGNC Symbol;Acc:HGNC:53395]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369996","summary":null,"start":114238970,"end":114241770,"strand":-1,"description":"long intergenic non-protein coding RNA 2459 [Source:HGNC Symbol;Acc:HGNC:53395]"}, {"versioned_ensembl_gene_id":"ENSG00000232435.1","gene_symbol":"DDX6P1","gene_name":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]","synonyms":"bA150A6.3,DDX6P,DDX6-Lp","biotype":"processed_pseudogene","ncbi_id":"442192","summary":null,"start":29329857,"end":29331292,"strand":-1,"description":"DEAD-box helicase 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13948]"}, {"versioned_ensembl_gene_id":"ENSG00000187173.3","gene_symbol":"LCE2A","gene_name":"late cornified envelope 2A [Source:HGNC Symbol;Acc:HGNC:29469]","synonyms":"LEP9","biotype":"protein_coding","ncbi_id":"353139","summary":null,"start":152698364,"end":152699442,"strand":1,"description":"late cornified envelope 2A [Source:HGNC Symbol;Acc:HGNC:29469]"}, {"versioned_ensembl_gene_id":"ENSG00000172689.1","gene_symbol":"MS4A10","gene_name":"membrane spanning 4-domains A10 [Source:HGNC Symbol;Acc:HGNC:13368]","synonyms":"MS4A9,CD20L7","biotype":"protein_coding","ncbi_id":"341116","summary":"Most MS4A genes, including MS4A10, encode proteins with at least 4 potential transmembrane domains and N- and C-terminal cytoplasmic domains encoded by distinct exons.[supplied by OMIM, Apr 2004]","start":60785348,"end":60801305,"strand":1,"description":"membrane spanning 4-domains A10 [Source:HGNC Symbol;Acc:HGNC:13368]"}, {"versioned_ensembl_gene_id":"ENSG00000216560.4","gene_symbol":"LINC00955","gene_name":"long intergenic non-protein coding RNA 955 [Source:HGNC Symbol;Acc:HGNC:26644]","synonyms":"FLJ35424","biotype":"processed_transcript","ncbi_id":"285492","summary":null,"start":3576869,"end":3590711,"strand":1,"description":"long intergenic non-protein coding RNA 955 [Source:HGNC Symbol;Acc:HGNC:26644]"}, {"versioned_ensembl_gene_id":"ENSG00000280326.1","gene_symbol":"AC067931.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":140591684,"end":140593201,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000251379.1","gene_symbol":"AC099550.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15358141,"end":15420032,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000174886.12","gene_symbol":"NDUFA11","gene_name":"NADH:ubiquinone oxidoreductase subunit A11 [Source:HGNC Symbol;Acc:HGNC:20371]","synonyms":"B14.7","biotype":"protein_coding","ncbi_id":"126328","summary":"This gene encodes a subunit of the membrane-bound mitochondrial complex I. Complex I is composed of numerous subunits and functions as the NADH-ubiquinol reductase of the mitochondrial electron transport chain. Mutations in this gene are associated with severe mitochondrial complex I deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]","start":5891276,"end":5904006,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A11 [Source:HGNC Symbol;Acc:HGNC:20371]"}, {"versioned_ensembl_gene_id":"ENSG00000123908.11","gene_symbol":"AGO2","gene_name":"argonaute 2, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:3263]","synonyms":"CASC7,Q10,LINC00980,hAGO2,EIF2C2","biotype":"protein_coding","ncbi_id":"27161","summary":"This gene encodes a member of the Argonaute family of proteins which play a role in RNA interference. The encoded protein is highly basic, and contains a PAZ domain and a PIWI domain. It may interact with dicer1 and play a role in short-interfering-RNA-mediated gene silencing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":140520156,"end":140635619,"strand":-1,"description":"argonaute 2, RISC catalytic component [Source:HGNC Symbol;Acc:HGNC:3263]"}, {"versioned_ensembl_gene_id":"ENSG00000114026.21","gene_symbol":"OGG1","gene_name":"8-oxoguanine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:8125]","synonyms":"HOGG1,HMMH,OGH1,MUTM","biotype":"protein_coding","ncbi_id":"4968","summary":"This gene encodes the enzyme responsible for the excision of 8-oxoguanine, a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen. The action of this enzyme includes lyase activity for chain cleavage. Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups, type 1 and type 2, depending on the last exon of the sequence. Type 1 alternative splice variants end with exon 7 and type 2 end with exon 8. All variants share the N-terminal region in common, which contains a mitochondrial targeting signal that is essential for mitochondrial localization. Many alternative splice variants for this gene have been described, but the full-length nature for every variant has not been determined. [provided by RefSeq, Aug 2008]","start":9749944,"end":9788219,"strand":1,"description":"8-oxoguanine DNA glycosylase [Source:HGNC Symbol;Acc:HGNC:8125]"}, {"versioned_ensembl_gene_id":"ENSG00000171103.10","gene_symbol":"TRMT61B","gene_name":"tRNA methyltransferase 61B [Source:HGNC Symbol;Acc:HGNC:26070]","synonyms":"FLJ20628","biotype":"protein_coding","ncbi_id":"55006","summary":null,"start":28849821,"end":28870301,"strand":-1,"description":"tRNA methyltransferase 61B [Source:HGNC Symbol;Acc:HGNC:26070]"}, {"versioned_ensembl_gene_id":"ENSG00000187170.4","gene_symbol":"LCE4A","gene_name":"late cornified envelope 4A [Source:HGNC Symbol;Acc:HGNC:16613]","synonyms":"SPRL4A,LEP8","biotype":"protein_coding","ncbi_id":"199834","summary":null,"start":152708160,"end":152709491,"strand":1,"description":"late cornified envelope 4A [Source:HGNC Symbol;Acc:HGNC:16613]"}, {"versioned_ensembl_gene_id":"ENSG00000231154.1","gene_symbol":"MORF4L2-AS1","gene_name":"MORF4L2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27991]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"340544","summary":null,"start":103687284,"end":103691772,"strand":1,"description":"MORF4L2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27991]"}, {"versioned_ensembl_gene_id":"ENSG00000100330.15","gene_symbol":"MTMR3","gene_name":"myotubularin related protein 3 [Source:HGNC Symbol;Acc:HGNC:7451]","synonyms":"ZFYVE10,KIAA0371,FYVE-DSP1","biotype":"protein_coding","ncbi_id":"8897","summary":"This gene encodes a member of the myotubularin dual specificity protein phosphatase gene family. The encoded protein is structurally similar to myotubularin but in addition contains a FYVE domain and an N-terminal PH-GRAM domain. The protein can self-associate and also form heteromers with another myotubularin related protein. The protein binds to phosphoinositide lipids through the PH-GRAM domain, and can hydrolyze phosphatidylinositol(3)-phosphate and phosphatidylinositol(3,5)-biphosphate in vitro. The encoded protein has been observed to have a perinuclear, possibly membrane-bound, distribution in cells, but it has also been found free in the cytoplasm. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":29883155,"end":30030866,"strand":1,"description":"myotubularin related protein 3 [Source:HGNC Symbol;Acc:HGNC:7451]"}, {"versioned_ensembl_gene_id":"ENSG00000123562.16","gene_symbol":"MORF4L2","gene_name":"mortality factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:16849]","synonyms":"MRGX,KIAA0026","biotype":"protein_coding","ncbi_id":"9643","summary":null,"start":103675496,"end":103688158,"strand":-1,"description":"mortality factor 4 like 2 [Source:HGNC Symbol;Acc:HGNC:16849]"}, {"versioned_ensembl_gene_id":"ENSG00000204692.9","gene_symbol":"OR12D3","gene_name":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]","synonyms":"hs6M1-27","biotype":"protein_coding","ncbi_id":"81797","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29373343,"end":29449876,"strand":-1,"description":"olfactory receptor family 12 subfamily D member 3 [Source:HGNC Symbol;Acc:HGNC:13963]"}, {"versioned_ensembl_gene_id":"ENSG00000260605.1","gene_symbol":"AC027688.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51035118,"end":51038764,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000261637.2","gene_symbol":"LINC02127","gene_name":"long intergenic non-protein coding RNA 2127 [Source:HGNC Symbol;Acc:HGNC:52985]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101927334","summary":null,"start":51017544,"end":51035777,"strand":1,"description":"long intergenic non-protein coding RNA 2127 [Source:HGNC Symbol;Acc:HGNC:52985]"}, {"versioned_ensembl_gene_id":"ENSG00000206472.11","gene_symbol":"OR11A1","gene_name":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]","synonyms":"OR11A2,hs6M1-18","biotype":"protein_coding","ncbi_id":"26531","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29425279,"end":29456852,"strand":-1,"description":"olfactory receptor family 11 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:8176]"}, {"versioned_ensembl_gene_id":"ENSG00000281385.2","gene_symbol":"AP2A2","gene_name":"adaptor related protein complex 2 alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:562]","synonyms":"HIP9,DKFZP564D1864,CLAPA2,ADTAB,KIAA0899,HYPJ","biotype":"protein_coding","ncbi_id":"161","summary":"The protein encoded by this gene is a subunit of the AP-2 adaptor protein complex, which is involved in linking lipid and protein membrane components with the clathrin lattice. This interaction supports the formation of clathrin-coated vesicles, and the encoded subunit aids in the process by binding polyphosphoinositide-containing lipids in the cell membrane. [provided by RefSeq, Nov 2016]","start":940735,"end":1019087,"strand":1,"description":"adaptor related protein complex 2 alpha 2 subunit [Source:HGNC Symbol;Acc:HGNC:562]"}, {"versioned_ensembl_gene_id":"ENSG00000255845.1","gene_symbol":"AP000777.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60813932,"end":60821739,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000260588.1","gene_symbol":"AC027702.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":41828165,"end":41829934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158828.7","gene_symbol":"PINK1","gene_name":"PTEN induced putative kinase 1 [Source:HGNC Symbol;Acc:HGNC:14581]","synonyms":"PARK6","biotype":"protein_coding","ncbi_id":"65018","summary":"This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008]","start":20633455,"end":20651511,"strand":1,"description":"PTEN induced putative kinase 1 [Source:HGNC Symbol;Acc:HGNC:14581]"}, {"versioned_ensembl_gene_id":"ENSG00000253389.2","gene_symbol":"AC113133.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41660991,"end":41665566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000079387.13","gene_symbol":"SENP1","gene_name":"SUMO1/sentrin specific peptidase 1 [Source:HGNC Symbol;Acc:HGNC:17927]","synonyms":null,"biotype":"protein_coding","ncbi_id":"29843","summary":"This gene encodes a cysteine protease that specifically targets members of the small ubiquitin-like modifier (SUMO) protein family. This protease regulates SUMO pathways by deconjugating sumoylated proteins. This protease also functions to process the precursor SUMO proteins into their mature form. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]","start":48042898,"end":48106308,"strand":-1,"description":"SUMO1/sentrin specific peptidase 1 [Source:HGNC Symbol;Acc:HGNC:17927]"}, {"versioned_ensembl_gene_id":"ENSG00000229713.1","gene_symbol":"AL353779.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152737518,"end":152737868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000204690.6","gene_symbol":"OR12D2","gene_name":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]","synonyms":"hs6M1-20","biotype":"protein_coding","ncbi_id":"26529","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":29396336,"end":29397404,"strand":1,"description":"olfactory receptor family 12 subfamily D member 2 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8178]"}, {"versioned_ensembl_gene_id":"ENSG00000132359.14","gene_symbol":"RAP1GAP2","gene_name":"RAP1 GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:29176]","synonyms":"KIAA1039,GARNL4","biotype":"protein_coding","ncbi_id":"23108","summary":"This gene encodes a GTPase-activating protein that activates the small guanine-nucleotide-binding protein Rap1 in platelets. The protein interacts with synaptotagmin-like protein 1 and Rab27 and regulates secretion of dense granules from platelets at sites of endothelial damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]","start":2755705,"end":3037739,"strand":1,"description":"RAP1 GTPase activating protein 2 [Source:HGNC Symbol;Acc:HGNC:29176]"}, {"versioned_ensembl_gene_id":"ENSG00000260620.1","gene_symbol":"AC027688.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":51054728,"end":51056399,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233819.1","gene_symbol":"AL353779.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":152744299,"end":152744606,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266941.1","gene_symbol":"AC024592.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":5899895,"end":5901511,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000258359.1","gene_symbol":"PCNPP1","gene_name":"PEST containing nuclear protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32440]","synonyms":"PCNPP","biotype":"processed_pseudogene","ncbi_id":"654427","summary":null,"start":111669852,"end":111670362,"strand":-1,"description":"PEST containing nuclear protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:32440]"}, {"versioned_ensembl_gene_id":"ENSG00000204689.7","gene_symbol":"OR10C1","gene_name":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]","synonyms":"hs6M1-17,OR10C2,OR10C1P","biotype":"protein_coding","ncbi_id":"442194","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jul 2015]","start":29439082,"end":29440753,"strand":1,"description":"olfactory receptor family 10 subfamily C member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8165]"}, {"versioned_ensembl_gene_id":"ENSG00000130383.7","gene_symbol":"FUT5","gene_name":"fucosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4016]","synonyms":"FUC-TV","biotype":"protein_coding","ncbi_id":"2527","summary":null,"start":5865826,"end":5870540,"strand":-1,"description":"fucosyltransferase 5 [Source:HGNC Symbol;Acc:HGNC:4016]"}, {"versioned_ensembl_gene_id":"ENSG00000203786.6","gene_symbol":"KPRP","gene_name":"keratinocyte proline rich protein [Source:HGNC Symbol;Acc:HGNC:31823]","synonyms":"C1orf45","biotype":"protein_coding","ncbi_id":"448834","summary":"This gene encodes a proline-rich skin protein possibly involved in keratinocyte differentiation. [provided by RefSeq, Jul 2016]","start":152759561,"end":152762052,"strand":1,"description":"keratinocyte proline rich protein [Source:HGNC Symbol;Acc:HGNC:31823]"}, {"versioned_ensembl_gene_id":"ENSG00000179163.11","gene_symbol":"FUCA1","gene_name":"fucosidase, alpha-L- 1, tissue [Source:HGNC Symbol;Acc:HGNC:4006]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2517","summary":"The protein encoded by this gene is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. Mutations in this gene are associated with fucosidosis (FUCA1D), which is an autosomal recessive lysosomal storage disease. A pseudogene of this locus is present on chr 2.[provided by RefSeq, Oct 2009]","start":23845077,"end":23868294,"strand":-1,"description":"fucosidase, alpha-L- 1, tissue [Source:HGNC Symbol;Acc:HGNC:4006]"}, {"versioned_ensembl_gene_id":"ENSG00000110104.11","gene_symbol":"CCDC86","gene_name":"coiled-coil domain containing 86 [Source:HGNC Symbol;Acc:HGNC:28359]","synonyms":"MGC2574","biotype":"protein_coding","ncbi_id":"79080","summary":null,"start":60842071,"end":60851081,"strand":1,"description":"coiled-coil domain containing 86 [Source:HGNC Symbol;Acc:HGNC:28359]"}, {"versioned_ensembl_gene_id":"ENSG00000224940.8","gene_symbol":"PRRT4","gene_name":"proline rich transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:37280]","synonyms":null,"biotype":"protein_coding","ncbi_id":"401399","summary":null,"start":128350325,"end":128361685,"strand":-1,"description":"proline rich transmembrane protein 4 [Source:HGNC Symbol;Acc:HGNC:37280]"}, {"versioned_ensembl_gene_id":"ENSG00000214114.8","gene_symbol":"MYCBP","gene_name":"MYC binding protein [Source:HGNC Symbol;Acc:HGNC:7554]","synonyms":"AMY-1","biotype":"protein_coding","ncbi_id":"26292","summary":"The protein encoded by this gene binds to the N-terminus of the oncogenic protein C-MYC, enhancing the ability of C-MYC to activate E box-dependent transcription. The encoded protein is normally found in the cytoplasm, but it translocates to the nucleus during S phase of the cell cycle and associates with C-MYC. This protein may be involved in spermatogenesis. This gene can be silenced by microRNA-22. Two transcript variants, one protein-coding and the other probably not protein-coding, have been found for this gene. [provided by RefSeq, Nov 2011]","start":38862964,"end":38874105,"strand":-1,"description":"MYC binding protein [Source:HGNC Symbol;Acc:HGNC:7554]"}, {"versioned_ensembl_gene_id":"ENSG00000249571.1","gene_symbol":"OR12D1","gene_name":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]","synonyms":"hs6M1-19,OR12D1P","biotype":"unprocessed_pseudogene","ncbi_id":"26530","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jan 2017]","start":29417055,"end":29418001,"strand":1,"description":"olfactory receptor family 12 subfamily D member 1 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:8177]"}, {"versioned_ensembl_gene_id":"ENSG00000261282.1","gene_symbol":"SOD1P2","gene_name":"superoxide dismutase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45135]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100652974","summary":null,"start":51107571,"end":51108021,"strand":1,"description":"superoxide dismutase 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45135]"}, {"versioned_ensembl_gene_id":"ENSG00000112461.9","gene_symbol":"OR5V1","gene_name":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]","synonyms":"hs6M1-21","biotype":"protein_coding","ncbi_id":"81696","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":29355463,"end":29431743,"strand":-1,"description":"olfactory receptor family 5 subfamily V member 1 [Source:HGNC Symbol;Acc:HGNC:13972]"}, {"versioned_ensembl_gene_id":"ENSG00000134216.18","gene_symbol":"CHIA","gene_name":"chitinase, acidic [Source:HGNC Symbol;Acc:HGNC:17432]","synonyms":"TSA1902,CHIT2,AMCase","biotype":"protein_coding","ncbi_id":"27159","summary":"The protein encoded by this gene degrades chitin, which is found in the cell wall of most fungi as well as in arthropods and some nematodes. The encoded protein can also stimulate interleukin 13 expression, and variations in this gene can lead to asthma susceptibility. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]","start":111290862,"end":111320566,"strand":1,"description":"chitinase, acidic [Source:HGNC Symbol;Acc:HGNC:17432]"}, {"versioned_ensembl_gene_id":"ENSG00000283078.1","gene_symbol":"AL137077.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":62066830,"end":62068437,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000267740.5","gene_symbol":"AC024592.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":5866171,"end":5903787,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000240386.3","gene_symbol":"LCE1F","gene_name":"late cornified envelope 1F [Source:HGNC Symbol;Acc:HGNC:29467]","synonyms":"LEP6","biotype":"protein_coding","ncbi_id":"353137","summary":null,"start":152776372,"end":152776728,"strand":1,"description":"late cornified envelope 1F [Source:HGNC Symbol;Acc:HGNC:29467]"}, {"versioned_ensembl_gene_id":"ENSG00000282828.1","gene_symbol":"AC009971.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":49563398,"end":49595122,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000244038.9","gene_symbol":"DDOST","gene_name":"dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:2728]","synonyms":"OST48,OST,KIAA0115,GATD6,WBP1","biotype":"protein_coding","ncbi_id":"1650","summary":"This gene encodes a component of the oligosaccharyltransferase complex which catalyzes the transfer of high-mannose oligosaccharides to asparagine residues on nascent polypeptides in the lumen of the rough endoplasmic reticulum. The protein complex co-purifies with ribosomes. The product of this gene is also implicated in the processing of advanced glycation endproducts (AGEs), which form from non-enzymatic reactions between sugars and proteins or lipids and are associated with aging and hyperglycemia. [provided by RefSeq, Jul 2008]","start":20651767,"end":20661544,"strand":-1,"description":"dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit [Source:HGNC Symbol;Acc:HGNC:2728]"}, {"versioned_ensembl_gene_id":"ENSG00000124116.18","gene_symbol":"WFDC3","gene_name":"WAP four-disulfide core domain 3 [Source:HGNC Symbol;Acc:HGNC:15957]","synonyms":"WAP14,dJ447F3.3","biotype":"protein_coding","ncbi_id":"140686","summary":"This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. The encoded protein contains four WFDC domains. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Alternatively spliced transcript variants have been observed but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]","start":45747944,"end":45791932,"strand":-1,"description":"WAP four-disulfide core domain 3 [Source:HGNC Symbol;Acc:HGNC:15957]"}, {"versioned_ensembl_gene_id":"ENSG00000232557.3","gene_symbol":"AL590609.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":23907111,"end":23907885,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188822.7","gene_symbol":"CNR2","gene_name":"cannabinoid receptor 2 [Source:HGNC Symbol;Acc:HGNC:2160]","synonyms":"CB2","biotype":"protein_coding","ncbi_id":"1269","summary":"The cannabinoid delta-9-tetrahydrocannabinol is the principal psychoactive ingredient of marijuana. The proteins encoded by this gene and the cannabinoid receptor 1 (brain) (CNR1) gene have the characteristics of a guanine nucleotide-binding protein (G-protein)-coupled receptor for cannabinoids. They inhibit adenylate cyclase activity in a dose-dependent, stereoselective, and pertussis toxin-sensitive manner. These proteins have been found to be involved in the cannabinoid-induced CNS effects (including alterations in mood and cognition) experienced by users of marijuana. The cannabinoid receptors are members of family 1 of the G-protein-coupled receptors. [provided by RefSeq, Jul 2008]","start":23870526,"end":23913362,"strand":-1,"description":"cannabinoid receptor 2 [Source:HGNC Symbol;Acc:HGNC:2160]"}, {"versioned_ensembl_gene_id":"ENSG00000282021.1","gene_symbol":"AC100810.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1758208,"end":1760447,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000104728.15","gene_symbol":"ARHGEF10","gene_name":"Rho guanine nucleotide exchange factor 10 [Source:HGNC Symbol;Acc:HGNC:14103]","synonyms":"KIAA0294,Gef10","biotype":"protein_coding","ncbi_id":"9639","summary":"This gene encodes a Rho guanine nucleotide exchange factor (GEF). Rho GEFs regulate the activity of small Rho GTPases by stimulating the exchange of guanine diphosphate (GDP) for guanine triphosphate (GTP) and may play a role in neural morphogenesis. Mutations in this gene are associated with slowed nerve conduction velocity (SNCV). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":1823976,"end":1958641,"strand":1,"description":"Rho guanine nucleotide exchange factor 10 [Source:HGNC Symbol;Acc:HGNC:14103]"}, {"versioned_ensembl_gene_id":"ENSG00000089225.19","gene_symbol":"TBX5","gene_name":"T-box 5 [Source:HGNC Symbol;Acc:HGNC:11604]","synonyms":"HOS","biotype":"protein_coding","ncbi_id":"6910","summary":"This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":114353931,"end":114408442,"strand":-1,"description":"T-box 5 [Source:HGNC Symbol;Acc:HGNC:11604]"}, {"versioned_ensembl_gene_id":"ENSG00000229106.1","gene_symbol":"BTBD6P1","gene_name":"BTB domain containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51542]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"646330","summary":null,"start":23901471,"end":23902737,"strand":-1,"description":"BTB domain containing 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:51542]"}, {"versioned_ensembl_gene_id":"ENSG00000234253.1","gene_symbol":"RPL7P13","gene_name":"ribosomal protein L7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36861]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"130728","summary":null,"start":49878623,"end":49879363,"strand":1,"description":"ribosomal protein L7 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:36861]"}, {"versioned_ensembl_gene_id":"ENSG00000158315.10","gene_symbol":"RHBDL2","gene_name":"rhomboid like 2 [Source:HGNC Symbol;Acc:HGNC:16083]","synonyms":"FLJ20435","biotype":"protein_coding","ncbi_id":"54933","summary":"The protein encoded by this gene is a member of the rhomboid family of integral membrane proteins. This family contains proteins that are related to Drosophila rhomboid protein. Members of this family are found in both prokaryotes and eukaryotes and are thought to function as intramembrane serine proteases. The encoded protein is thought to release soluble growth factors by proteolytic cleavage of certain membrane-bound substrates, including ephrin B2 and ephrin B3. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2015]","start":38885807,"end":38941799,"strand":-1,"description":"rhomboid like 2 [Source:HGNC Symbol;Acc:HGNC:16083]"}, {"versioned_ensembl_gene_id":"ENSG00000203307.2","gene_symbol":"AL626787.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":166081183,"end":166087483,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000125844.15","gene_symbol":"RRBP1","gene_name":"ribosome binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10448]","synonyms":"hES,ES/130","biotype":"protein_coding","ncbi_id":"6238","summary":"This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012]","start":17613678,"end":17682295,"strand":-1,"description":"ribosome binding protein 1 [Source:HGNC Symbol;Acc:HGNC:10448]"}, {"versioned_ensembl_gene_id":"ENSG00000273637.1","gene_symbol":"AL139260.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":38839333,"end":38874494,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000273233.1","gene_symbol":"AC097724.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":28810281,"end":28810706,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000163806.15","gene_symbol":"SPDYA","gene_name":"speedy/RINGO cell cycle regulator family member A [Source:HGNC Symbol;Acc:HGNC:30613]","synonyms":"SPY1,SPDY1,Ringo3","biotype":"protein_coding","ncbi_id":"245711","summary":null,"start":28782517,"end":28850611,"strand":1,"description":"speedy/RINGO cell cycle regulator family member A [Source:HGNC Symbol;Acc:HGNC:30613]"}, {"versioned_ensembl_gene_id":"ENSG00000224690.2","gene_symbol":"UBE2D3P3","gene_name":"ubiquitin conjugating enzyme E2 D3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39011]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874262","summary":null,"start":150800473,"end":150801031,"strand":1,"description":"ubiquitin conjugating enzyme E2 D3 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:39011]"}, {"versioned_ensembl_gene_id":"ENSG00000228436.2","gene_symbol":"AL139260.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38860000,"end":38919396,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000143387.12","gene_symbol":"CTSK","gene_name":"cathepsin K [Source:HGNC Symbol;Acc:HGNC:2536]","synonyms":"PYCD,PKND,CTSO2,CTSO","biotype":"protein_coding","ncbi_id":"1513","summary":"The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. [provided by RefSeq, Apr 2013]","start":150796208,"end":150808323,"strand":-1,"description":"cathepsin K [Source:HGNC Symbol;Acc:HGNC:2536]"}, {"versioned_ensembl_gene_id":"ENSG00000102302.7","gene_symbol":"FGD1","gene_name":"FYVE, RhoGEF and PH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:3663]","synonyms":"ZFYVE3,FGDY","biotype":"protein_coding","ncbi_id":"2245","summary":"This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of the faciogenital dysplasia in Aarskog-Scott syndrome and a syndromatic form of X-linked cognitive disability. [provided by RefSeq, Jul 2017]","start":54445454,"end":54496166,"strand":-1,"description":"FYVE, RhoGEF and PH domain containing 1 [Source:HGNC Symbol;Acc:HGNC:3663]"}, {"versioned_ensembl_gene_id":"ENSG00000132881.11","gene_symbol":"RSG1","gene_name":"REM2 and RAB like small GTPase 1 [Source:HGNC Symbol;Acc:HGNC:28127]","synonyms":"MGC10731,C1orf89","biotype":"protein_coding","ncbi_id":"79363","summary":null,"start":16231700,"end":16237162,"strand":-1,"description":"REM2 and RAB like small GTPase 1 [Source:HGNC Symbol;Acc:HGNC:28127]"}, {"versioned_ensembl_gene_id":"ENSG00000124092.12","gene_symbol":"CTCFL","gene_name":"CCCTC-binding factor like [Source:HGNC Symbol;Acc:HGNC:16234]","synonyms":"dJ579F20.2,CT27,BORIS","biotype":"protein_coding","ncbi_id":"140690","summary":"CCCTC-binding factor (CTCF), an 11-zinc-finger factor involved in gene regulation, utilizes different zinc fingers to bind varying DNA target sites. CTCF forms methylation-sensitive insulators that regulate X-chromosome inactivation. This gene is a paralog of CTCF and appears to be expressed primarily in the cytoplasm of spermatocytes, unlike CTCF which is expressed primarily in the nucleus of somatic cells. CTCF and the protein encoded by this gene are normally expressed in a mutually exclusive pattern that correlates with resetting of methylation marks during male germ cell differentiation. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]","start":57495966,"end":57525652,"strand":-1,"description":"CCCTC-binding factor like [Source:HGNC Symbol;Acc:HGNC:16234]"}, {"versioned_ensembl_gene_id":"ENSG00000140254.12","gene_symbol":"DUOXA1","gene_name":"dual oxidase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:26507]","synonyms":"NUMBIP,NIP,mol,FLJ32334","biotype":"protein_coding","ncbi_id":"90527","summary":"Dual oxidases DUOX1 and DUOX2 are NADPH oxidases which are involved in hydrogen peroxide production necessary for thyroid hormonogenesis. They form a heterodimer with specific maturation factors DUOXA1 and DUOXA2, respectively, which is essential for the maturation and function of the DUOX enzyme complexes. This gene encodes the DUOX1 activator or maturation factor DUOXA1. Rat studies identified a bidirectional promoter which controls the transcription of the DUOX1 and DUOXA1 genes. This protein is cotransported to the cell surface when coexpressed with DUOX1 and is retained in the endoplasmic reticulum when expressed without DUOX1 protein. The expression of this gene or the DUOX1 gene is not suppressed by thyroglobulin (Tg), a macromolecular precursor in thyroid hormone synthesis, while the expression of the DUOX2 and DUOXA2 are significantly suppressed by the Tg. This protein is also a p53-regulated neurogenic factor involved in p53 dependent neuronal differentiation. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013]","start":45117367,"end":45129938,"strand":-1,"description":"dual oxidase maturation factor 1 [Source:HGNC Symbol;Acc:HGNC:26507]"}, {"versioned_ensembl_gene_id":"ENSG00000255959.1","gene_symbol":"AP000777.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60835996,"end":60842965,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000183134.4","gene_symbol":"PTGDR2","gene_name":"prostaglandin D2 receptor 2 [Source:HGNC Symbol;Acc:HGNC:4502]","synonyms":"CRTH2,CD294,GPR44,DP2","biotype":"protein_coding","ncbi_id":"11251","summary":"This gene encodes a G-protein-coupled receptor that is preferentially expressed in CD4+ effector T helper 2 (Th2) cells. This protein is a prostaglandin D2 receptor that mediates the pro-inflammatory chemotaxis of eosinophils, basophils, and Th2 lymphocytes generated during allergic inflammation. Single nucleotide polymorphisms in the 3' UTR of this gene have been associated with asthma susceptibility.[provided by RefSeq, Mar 2011]","start":60850940,"end":60855971,"strand":-1,"description":"prostaglandin D2 receptor 2 [Source:HGNC Symbol;Acc:HGNC:4502]"}, {"versioned_ensembl_gene_id":"ENSG00000274944.4","gene_symbol":"AL139260.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38864501,"end":38881617,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000256813.1","gene_symbol":"AP000777.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":60841806,"end":60851081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000271527.1","gene_symbol":"AL606495.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":165941235,"end":165941769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000226292.1","gene_symbol":"AL606495.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166022215,"end":166023027,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000131233.9","gene_symbol":"GJA9","gene_name":"gap junction protein alpha 9 [Source:HGNC Symbol;Acc:HGNC:19155]","synonyms":"GJA10,CX59,CX58","biotype":"protein_coding","ncbi_id":"81025","summary":"Connexins, such as GJA9, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]","start":38874451,"end":38881587,"strand":-1,"description":"gap junction protein alpha 9 [Source:HGNC Symbol;Acc:HGNC:19155]"}, {"versioned_ensembl_gene_id":"ENSG00000230898.1","gene_symbol":"AL596087.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":166147782,"end":166165095,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000188859.6","gene_symbol":"FAM78B","gene_name":"family with sequence similarity 78 member B [Source:HGNC Symbol;Acc:HGNC:13495]","synonyms":null,"biotype":"protein_coding","ncbi_id":"149297","summary":null,"start":166057426,"end":166166969,"strand":-1,"description":"family with sequence similarity 78 member B [Source:HGNC Symbol;Acc:HGNC:13495]"}, {"versioned_ensembl_gene_id":"ENSG00000274935.5","gene_symbol":"LILRA1","gene_name":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]","synonyms":"LIR-6,CD85i,LIR6","biotype":"protein_coding","ncbi_id":"11024","summary":"This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]","start":54525581,"end":54534404,"strand":1,"description":"leukocyte immunoglobulin like receptor A1 [Source:HGNC Symbol;Acc:HGNC:6602]"}, {"versioned_ensembl_gene_id":"ENSG00000186998.15","gene_symbol":"EMID1","gene_name":"EMI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18036]","synonyms":"EMU1,EMI5,hEmu1","biotype":"protein_coding","ncbi_id":"129080","summary":null,"start":29205851,"end":29259597,"strand":1,"description":"EMI domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18036]"}, {"versioned_ensembl_gene_id":"ENSG00000116954.7","gene_symbol":"RRAGC","gene_name":"Ras related GTP binding C [Source:HGNC Symbol;Acc:HGNC:19902]","synonyms":"GTR2,FLJ13311","biotype":"protein_coding","ncbi_id":"64121","summary":"This gene encodes a member of the GTR/RAG GTP-binding protein family. The encoded protein is a monomeric guanine nucleotide-binding protein which forms a heterodimer with RRAGA and RRAGB and is primarily localized to the cytoplasm. The encoded protein promotes intracellular localization of the mTOR complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","start":38838198,"end":38859823,"strand":-1,"description":"Ras related GTP binding C [Source:HGNC Symbol;Acc:HGNC:19902]"}, {"versioned_ensembl_gene_id":"ENSG00000263011.1","gene_symbol":"AC108134.4","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":3106764,"end":3109576,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000117242.7","gene_symbol":"PINK1-AS","gene_name":"PINK1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:38872]","synonyms":"FLJ00387,PINK1AS,PINK1-AS1,naPINK1","biotype":"antisense_RNA","ncbi_id":"100861548","summary":null,"start":20642657,"end":20652193,"strand":-1,"description":"PINK1 antisense RNA [Source:HGNC Symbol;Acc:HGNC:38872]"}, {"versioned_ensembl_gene_id":"ENSG00000149506.11","gene_symbol":"ZP1","gene_name":"zona pellucida glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:13187]","synonyms":null,"biotype":"protein_coding","ncbi_id":"22917","summary":"The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed primarily of three or four glycoproteins with various functions during fertilization and preimplantation development. The protein encoded by this gene ensures the structural integrity of the zona pellucida. Mutations in this gene are a cause of oocyte maturation defect and infertility. [provided by RefSeq, May 2014]","start":60867562,"end":60875693,"strand":1,"description":"zona pellucida glycoprotein 1 [Source:HGNC Symbol;Acc:HGNC:13187]"}, {"versioned_ensembl_gene_id":"ENSG00000215457.5","gene_symbol":"AC022701.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":51845007,"end":51845628,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266335.1","gene_symbol":"AC016383.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":52336361,"end":52339025,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000158526.7","gene_symbol":"TSR2","gene_name":"TSR2, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:25455]","synonyms":"WGG1,RP1-112K5.2,DT1P1A10","biotype":"protein_coding","ncbi_id":"90121","summary":"The protein encoded by this gene appears to repress the transcription of NF-kappaB and may be involved in apoptosis. Defects in this gene are a cause of Diamond-Blackfan anemia. [provided by RefSeq, Oct 2016]","start":54440401,"end":54445487,"strand":1,"description":"TSR2, ribosome maturation factor [Source:HGNC Symbol;Acc:HGNC:25455]"}, {"versioned_ensembl_gene_id":"ENSG00000226454.1","gene_symbol":"AL033380.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40516336,"end":40523933,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185950.8","gene_symbol":"IRS2","gene_name":"insulin receptor substrate 2 [Source:HGNC Symbol;Acc:HGNC:6126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8660","summary":"This gene encodes the insulin receptor substrate 2, a cytoplasmic signaling molecule that mediates effects of insulin, insulin-like growth factor 1, and other cytokines by acting as a molecular adaptor between diverse receptor tyrosine kinases and downstream effectors. The product of this gene is phosphorylated by the insulin receptor tyrosine kinase upon receptor stimulation, as well as by an interleukin 4 receptor-associated kinase in response to IL4 treatment. [provided by RefSeq, Jul 2008]","start":109752698,"end":109786568,"strand":-1,"description":"insulin receptor substrate 2 [Source:HGNC Symbol;Acc:HGNC:6126]"}, {"versioned_ensembl_gene_id":"ENSG00000230881.1","gene_symbol":"AL445933.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41535443,"end":41535868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000127124.14","gene_symbol":"HIVEP3","gene_name":"human immunodeficiency virus type I enhancer binding protein 3 [Source:HGNC Symbol;Acc:HGNC:13561]","synonyms":"FLJ16752,ZNF40C,ZAS3,SHN3,Schnurri-3,KRC,KBP1,KIAA1555,KBP-1","biotype":"protein_coding","ncbi_id":"59269","summary":"This gene encodes a member of the human immunodeficiency virus type 1 enhancer-binding protein family. Members of this protein family contain multiple zinc finger and acid-rich (ZAS) domains and serine-threonine rich regions. This protein acts as a transcription factor and is able to regulate nuclear factor kappaB-mediated transcription by binding the kappaB motif in target genes. This protein also binds the recombination signal sequence that flanks the V, D, and J regions of immunoglobulin and T-cell receptors. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Sep 2011]","start":41506365,"end":42035925,"strand":-1,"description":"human immunodeficiency virus type I enhancer binding protein 3 [Source:HGNC Symbol;Acc:HGNC:13561]"}, {"versioned_ensembl_gene_id":"ENSG00000156564.8","gene_symbol":"LRFN2","gene_name":"leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21226]","synonyms":"SALM1,KIAA1246,FIGLER2","biotype":"protein_coding","ncbi_id":"57497","summary":null,"start":40391586,"end":40587465,"strand":-1,"description":"leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:HGNC:21226]"}, {"versioned_ensembl_gene_id":"ENSG00000236075.1","gene_symbol":"AL359475.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":40501631,"end":40502393,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250681.1","gene_symbol":"AL121796.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3633029,"end":3633975,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250632.1","gene_symbol":"LINC02171","gene_name":"long intergenic non-protein coding RNA 2171 [Source:HGNC Symbol;Acc:HGNC:53033]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100133461","summary":null,"start":3673593,"end":3677855,"strand":-1,"description":"long intergenic non-protein coding RNA 2171 [Source:HGNC Symbol;Acc:HGNC:53033]"}, {"versioned_ensembl_gene_id":"ENSG00000230228.2","gene_symbol":"AL590609.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23949016,"end":23949383,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000062650.18","gene_symbol":"WAPL","gene_name":"WAPL cohesin release factor [Source:HGNC Symbol;Acc:HGNC:23293]","synonyms":"WAPAL,KIAA0261,FOE","biotype":"protein_coding","ncbi_id":"23063","summary":null,"start":86435256,"end":86521815,"strand":-1,"description":"WAPL cohesin release factor [Source:HGNC Symbol;Acc:HGNC:23293]"}, {"versioned_ensembl_gene_id":"ENSG00000275248.1","gene_symbol":"AL355810.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":109805317,"end":109805868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000189266.11","gene_symbol":"PNRC2","gene_name":"proline rich nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:23158]","synonyms":null,"biotype":"protein_coding","ncbi_id":"55629","summary":null,"start":23959109,"end":23963462,"strand":1,"description":"proline rich nuclear receptor coactivator 2 [Source:HGNC Symbol;Acc:HGNC:23158]"}, {"versioned_ensembl_gene_id":"ENSG00000226138.4","gene_symbol":"AC004801.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":48085062,"end":48085421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230467.8","gene_symbol":"RNF39","gene_name":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]","synonyms":"LIRF,HZFw1","biotype":"protein_coding","ncbi_id":"80352","summary":"This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":30060650,"end":30066271,"strand":-1,"description":"ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]"}, {"versioned_ensembl_gene_id":"ENSG00000084731.14","gene_symbol":"KIF3C","gene_name":"kinesin family member 3C [Source:HGNC Symbol;Acc:HGNC:6321]","synonyms":null,"biotype":"protein_coding","ncbi_id":"3797","summary":null,"start":25926596,"end":25982749,"strand":-1,"description":"kinesin family member 3C [Source:HGNC Symbol;Acc:HGNC:6321]"}, {"versioned_ensembl_gene_id":"ENSG00000240399.1","gene_symbol":"AC004801.2","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":48054813,"end":48055591,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000250986.1","gene_symbol":"AC141928.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":3758748,"end":3763390,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275741.1","gene_symbol":"AL162497.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":109785831,"end":109808252,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000213639.9","gene_symbol":"PPP1CB","gene_name":"protein phosphatase 1 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9282]","synonyms":"PP1beta,PP1B,PP-1B","biotype":"protein_coding","ncbi_id":"5500","summary":"The protein encoded by this gene is one of the three catalytic subunits of protein phosphatase 1 (PP1). PP1 is a serine/threonine specific protein phosphatase known to be involved in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription. Mouse studies suggest that PP1 functions as a suppressor of learning and memory. Two alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]","start":28751640,"end":28802940,"strand":1,"description":"protein phosphatase 1 catalytic subunit beta [Source:HGNC Symbol;Acc:HGNC:9282]"}, {"versioned_ensembl_gene_id":"ENSG00000204839.8","gene_symbol":"MROH6","gene_name":"maestro heat like repeat family member 6 [Source:HGNC Symbol;Acc:HGNC:27814]","synonyms":"C8orf73","biotype":"protein_coding","ncbi_id":"642475","summary":null,"start":143566187,"end":143572971,"strand":-1,"description":"maestro heat like repeat family member 6 [Source:HGNC Symbol;Acc:HGNC:27814]"}, {"versioned_ensembl_gene_id":"ENSG00000230638.4","gene_symbol":"AL445933.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":41542069,"end":41544310,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000152556.15","gene_symbol":"PFKM","gene_name":"phosphofructokinase, muscle [Source:HGNC Symbol;Acc:HGNC:8877]","synonyms":"PPP1R122,PFKX,PFK-1","biotype":"protein_coding","ncbi_id":"5213","summary":"Three phosphofructokinase isozymes exist in humans: muscle, liver and platelet. These isozymes function as subunits of the mammalian tetramer phosphofructokinase, which catalyzes the phosphorylation of fructose-6-phosphate to fructose-1,6-bisphosphate. Tetramer composition varies depending on tissue type. This gene encodes the muscle-type isozyme. Mutations in this gene have been associated with glycogen storage disease type VII, also known as Tarui disease. Alternatively spliced transcript variants have been described.[provided by RefSeq, Nov 2009]","start":48105139,"end":48146404,"strand":1,"description":"phosphofructokinase, muscle [Source:HGNC Symbol;Acc:HGNC:8877]"}, {"versioned_ensembl_gene_id":"ENSG00000227846.1","gene_symbol":"UGT1A11P","gene_name":"UDP glucuronosyltransferase family 1 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:12532]","synonyms":"UGT1K","biotype":"unprocessed_pseudogene","ncbi_id":"54574","summary":null,"start":233603553,"end":233604401,"strand":1,"description":"UDP glucuronosyltransferase family 1 member A11, pseudogene [Source:HGNC Symbol;Acc:HGNC:12532]"}, {"versioned_ensembl_gene_id":"ENSG00000270522.1","gene_symbol":"AL162713.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":43787591,"end":43787852,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000255399.3","gene_symbol":"TBX5-AS1","gene_name":"TBX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27402]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"255480","summary":null,"start":114408191,"end":114412831,"strand":1,"description":"TBX5 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:27402]"}, {"versioned_ensembl_gene_id":"ENSG00000005175.9","gene_symbol":"RPAP3","gene_name":"RNA polymerase II associated protein 3 [Source:HGNC Symbol;Acc:HGNC:26151]","synonyms":"hSpagh,FLJ21908,spag","biotype":"protein_coding","ncbi_id":"79657","summary":"This gene encodes an RNA polymerase II-associated protein. The encoded protein may function in transcriptional regulation and may also regulate apoptosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":47661249,"end":47706061,"strand":-1,"description":"RNA polymerase II associated protein 3 [Source:HGNC Symbol;Acc:HGNC:26151]"}, {"versioned_ensembl_gene_id":"ENSG00000216676.2","gene_symbol":"AL031229.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27652602,"end":27652825,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000168630.3","gene_symbol":"SPINT5P","gene_name":"serine peptidase inhibitor, Kunitz type 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:16161]","synonyms":"dJ447F3.6,C20orf168","biotype":"processed_pseudogene","ncbi_id":"140863","summary":null,"start":45749920,"end":45750074,"strand":1,"description":"serine peptidase inhibitor, Kunitz type 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:16161]"}, {"versioned_ensembl_gene_id":"ENSG00000237829.6","gene_symbol":"PPP1R11","gene_name":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]","synonyms":"CFAP255,HCGV,Tctex5,HCG-V,TCTE5","biotype":"protein_coding","ncbi_id":"6992","summary":"This gene encodes a specific inhibitor of protein phosphatase-1 (PP1) with a differential sensitivity toward the metal-independent and metal-dependent forms of PP1. The gene is located within the major histocompatibility complex class I region on chromosome 6. [provided by RefSeq, Jul 2008]","start":30057093,"end":30060717,"strand":1,"description":"protein phosphatase 1 regulatory inhibitor subunit 11 [Source:HGNC Symbol;Acc:HGNC:9285]"}, {"versioned_ensembl_gene_id":"ENSG00000246820.2","gene_symbol":"AC091013.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":8169167,"end":8178903,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236944.1","gene_symbol":"CCDC58P2","gene_name":"coiled-coil domain containing 58 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45025]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100287708","summary":null,"start":50962993,"end":50963358,"strand":-1,"description":"coiled-coil domain containing 58 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45025]"}, {"versioned_ensembl_gene_id":"ENSG00000112214.10","gene_symbol":"FHL5","gene_name":"four and a half LIM domains 5 [Source:HGNC Symbol;Acc:HGNC:17371]","synonyms":"FLJ33049,dJ393D12.2,ACT","biotype":"protein_coding","ncbi_id":"9457","summary":"The protein encoded by this gene is coordinately expressed with activator of cAMP-responsive element modulator (CREM). It is associated with CREM and confers a powerful transcriptional activation function. CREM acts as a transcription factor essential for the differentiation of spermatids into mature spermatozoa. There are multiple polyadenylation sites found in this gene. Polymorphisms in this gene may be associated with susceptibility for migraine headaches. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Apr 2016]","start":96562548,"end":96616636,"strand":1,"description":"four and a half LIM domains 5 [Source:HGNC Symbol;Acc:HGNC:17371]"}, {"versioned_ensembl_gene_id":"ENSG00000259393.2","gene_symbol":"AC025918.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":58967046,"end":58967808,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241627.3","gene_symbol":"UBQLN4P1","gene_name":"ubiquilin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31133]","synonyms":"UBQLN4P,C3orf12","biotype":"processed_pseudogene","ncbi_id":"285329","summary":null,"start":148985868,"end":148987668,"strand":-1,"description":"ubiquilin 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:31133]"}, {"versioned_ensembl_gene_id":"ENSG00000128923.10","gene_symbol":"MINDY2","gene_name":"MINDY lysine 48 deubiquitinase 2 [Source:HGNC Symbol;Acc:HGNC:26954]","synonyms":"KIAA1164,FAM63B","biotype":"protein_coding","ncbi_id":"54629","summary":null,"start":58771192,"end":58861900,"strand":1,"description":"MINDY lysine 48 deubiquitinase 2 [Source:HGNC Symbol;Acc:HGNC:26954]"}, {"versioned_ensembl_gene_id":"ENSG00000186226.8","gene_symbol":"LCE1E","gene_name":"late cornified envelope 1E [Source:HGNC Symbol;Acc:HGNC:29466]","synonyms":"LEP5","biotype":"protein_coding","ncbi_id":"353135","summary":null,"start":152786214,"end":152788426,"strand":1,"description":"late cornified envelope 1E [Source:HGNC Symbol;Acc:HGNC:29466]"}, {"versioned_ensembl_gene_id":"ENSG00000223802.7","gene_symbol":"CERS1","gene_name":"ceramide synthase 1 [Source:HGNC Symbol;Acc:HGNC:14253]","synonyms":"UOG1,LASS1,LAG1","biotype":"protein_coding","ncbi_id":"10715","summary":"This gene encodes a ceramide synthase enzyme, which catalyzes the synthesis of ceramide, the hydrophobic moiety of sphingolipids. The encoded enzyme synthesizes 18-carbon (C18) ceramide in brain neurons. Elevated expression of this gene may be associated with increased longevity, while decreased expression of this gene may be associated with myoclonus epilepsy with dementia in human patients. This protein is transcribed from a monocistronic mRNA as well as a bicistronic mRNA, which also encodes growth differentiation factor 1. [provided by RefSeq, Jul 2016]","start":18868545,"end":18896727,"strand":-1,"description":"ceramide synthase 1 [Source:HGNC Symbol;Acc:HGNC:14253]"}, {"versioned_ensembl_gene_id":"ENSG00000082556.10","gene_symbol":"OPRK1","gene_name":"opioid receptor kappa 1 [Source:HGNC Symbol;Acc:HGNC:8154]","synonyms":"OPRK,KOR","biotype":"protein_coding","ncbi_id":"4986","summary":"This gene encodes an opioid receptor, which is a member of the 7 transmembrane-spanning G protein-coupled receptor family. It functions as a receptor for endogenous ligands, as well as a receptor for various synthetic opioids. Ligand binding results in inhibition of adenylate cyclase activity and neurotransmitter release. This opioid receptor plays a role in the perception of pain and mediating the hypolocomotor, analgesic and aversive actions of synthetic opioids. Variations in this gene have also been associated with alcohol dependence and opiate addiction. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]","start":53225716,"end":53251697,"strand":-1,"description":"opioid receptor kappa 1 [Source:HGNC Symbol;Acc:HGNC:8154]"}, {"versioned_ensembl_gene_id":"ENSG00000166407.13","gene_symbol":"LMO1","gene_name":"LIM domain only 1 [Source:HGNC Symbol;Acc:HGNC:6641]","synonyms":"TTG1,RHOM1,RBTN1","biotype":"protein_coding","ncbi_id":"4004","summary":"This locus encodes a transcriptional regulator that contains two cysteine-rich LIM domains but lacks a DNA-binding domain. LIM domains may play a role in protein interactions; thus the encoded protein may regulate transcription by competitively binding to specific DNA-binding transcription factors. Alterations at this locus have been associated with acute lymphoblastic T-cell leukemia. Chromosomal rearrangements have been observed between this locus and at least two loci, the delta subunit of the T-cell antigen receptor gene and the LIM domain binding 1 gene. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2012]","start":8224304,"end":8268716,"strand":-1,"description":"LIM domain only 1 [Source:HGNC Symbol;Acc:HGNC:6641]"}, {"versioned_ensembl_gene_id":"ENSG00000126903.15","gene_symbol":"SLC10A3","gene_name":"solute carrier family 10 member 3 [Source:HGNC Symbol;Acc:HGNC:22979]","synonyms":"P3,DXS253E","biotype":"protein_coding","ncbi_id":"8273","summary":"This gene maps to a GC-rich region of the X chromosome and was identified by its proximity to a CpG island. It is thought to be a housekeeping gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2008]","start":154487306,"end":154490690,"strand":-1,"description":"solute carrier family 10 member 3 [Source:HGNC Symbol;Acc:HGNC:22979]"}, {"versioned_ensembl_gene_id":"ENSG00000146151.12","gene_symbol":"HMGCLL1","gene_name":"3-hydroxymethyl-3-methylglutaryl-CoA lyase like 1 [Source:HGNC Symbol;Acc:HGNC:21359]","synonyms":"DKFZP434G1411,bA418P12.1","biotype":"protein_coding","ncbi_id":"54511","summary":null,"start":55434369,"end":55579214,"strand":-1,"description":"3-hydroxymethyl-3-methylglutaryl-CoA lyase like 1 [Source:HGNC Symbol;Acc:HGNC:21359]"}, {"versioned_ensembl_gene_id":"ENSG00000224055.1","gene_symbol":"GAPDHP55","gene_name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:38561]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421324","summary":null,"start":44063511,"end":44064313,"strand":1,"description":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 55 [Source:HGNC Symbol;Acc:HGNC:38561]"}, {"versioned_ensembl_gene_id":"ENSG00000261368.1","gene_symbol":"AL731537.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":50964270,"end":50965220,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000179611.3","gene_symbol":"DGKZP1","gene_name":"diacylglycerol kinase zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39263]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"400126","summary":null,"start":43968424,"end":43971199,"strand":1,"description":"diacylglycerol kinase zeta pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:39263]"}, {"versioned_ensembl_gene_id":"ENSG00000185607.5","gene_symbol":"ACTBP7","gene_name":"actin, beta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:140]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"67","summary":null,"start":43989061,"end":43990184,"strand":-1,"description":"actin, beta pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:140]"}, {"versioned_ensembl_gene_id":"ENSG00000233725.7","gene_symbol":"LINC00284","gene_name":"long intergenic non-protein coding RNA 284 [Source:HGNC Symbol;Acc:HGNC:26981]","synonyms":"NCRNA00284","biotype":"lincRNA","ncbi_id":"121838","summary":null,"start":43908669,"end":44030461,"strand":1,"description":"long intergenic non-protein coding RNA 284 [Source:HGNC Symbol;Acc:HGNC:26981]"}, {"versioned_ensembl_gene_id":"ENSG00000227973.1","gene_symbol":"PIN4P1","gene_name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44193]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"728758","summary":null,"start":43875849,"end":43876244,"strand":-1,"description":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44193]"}, {"versioned_ensembl_gene_id":"ENSG00000241828.2","gene_symbol":"AC006517.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7860437,"end":7860764,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000176654.12","gene_symbol":"NANOGP1","gene_name":"Nanog homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23099]","synonyms":"NANOG2","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"404635","summary":null,"start":7890801,"end":7900140,"strand":1,"description":"Nanog homeobox pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23099]"}, {"versioned_ensembl_gene_id":"ENSG00000171877.20","gene_symbol":"FRMD5","gene_name":"FERM domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28214]","synonyms":"MGC14161","biotype":"protein_coding","ncbi_id":"84978","summary":null,"start":43870761,"end":44195252,"strand":-1,"description":"FERM domain containing 5 [Source:HGNC Symbol;Acc:HGNC:28214]"}, {"versioned_ensembl_gene_id":"ENSG00000261238.1","gene_symbol":"AC009166.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":51149239,"end":51149819,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263080.1","gene_symbol":"AC009121.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11341809,"end":11345211,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000103449.11","gene_symbol":"SALL1","gene_name":"spalt like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10524]","synonyms":"TBS,Hsal1,ZNF794","biotype":"protein_coding","ncbi_id":"6299","summary":"The protein encoded by this gene is a zinc finger transcriptional repressor and may be part of the NuRD histone deacetylase complex (HDAC). Defects in this gene are a cause of Townes-Brocks syndrome (TBS) as well as bronchio-oto-renal syndrome (BOR). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":51135975,"end":51151367,"strand":-1,"description":"spalt like transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:10524]"}, {"versioned_ensembl_gene_id":"ENSG00000222020.2","gene_symbol":"AC062017.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":239401436,"end":239402364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178257.3","gene_symbol":"PRM3","gene_name":"protamine 3 [Source:HGNC Symbol;Acc:HGNC:13732]","synonyms":null,"biotype":"protein_coding","ncbi_id":"58531","summary":null,"start":11273218,"end":11273641,"strand":-1,"description":"protamine 3 [Source:HGNC Symbol;Acc:HGNC:13732]"}, {"versioned_ensembl_gene_id":"ENSG00000262703.1","gene_symbol":"AC009121.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":11348143,"end":11349321,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000178279.3","gene_symbol":"TNP2","gene_name":"transition protein 2 [Source:HGNC Symbol;Acc:HGNC:11952]","synonyms":"TP2","biotype":"protein_coding","ncbi_id":"7142","summary":null,"start":11267748,"end":11269533,"strand":-1,"description":"transition protein 2 [Source:HGNC Symbol;Acc:HGNC:11952]"}, {"versioned_ensembl_gene_id":"ENSG00000173262.11","gene_symbol":"SLC2A14","gene_name":"solute carrier family 2 member 14 [Source:HGNC Symbol;Acc:HGNC:18301]","synonyms":"SLC2A3P3,GLUT14","biotype":"protein_coding","ncbi_id":"144195","summary":"Members of the glucose transporter (GLUT) family, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as glucose and fructose into all mammalian cells. GLUTs show tissue and cell-type specific expression (Wu and Freeze, 2002 [PubMed 12504846]).[supplied by OMIM, Mar 2008]","start":7812512,"end":7891148,"strand":-1,"description":"solute carrier family 2 member 14 [Source:HGNC Symbol;Acc:HGNC:18301]"}, {"versioned_ensembl_gene_id":"ENSG00000278994.1","gene_symbol":"AC008785.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":18201501,"end":18201956,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000151773.12","gene_symbol":"CCDC122","gene_name":"coiled-coil domain containing 122 [Source:HGNC Symbol;Acc:HGNC:26478]","synonyms":"FLJ31846","biotype":"protein_coding","ncbi_id":"160857","summary":"This gene encodes a protein that contains a coiled-coil domain. Naturally occurring mutations in this gene are associated with leprosy. [provided by RefSeq, Apr 2017]","start":43823909,"end":43879727,"strand":-1,"description":"coiled-coil domain containing 122 [Source:HGNC Symbol;Acc:HGNC:26478]"}, {"versioned_ensembl_gene_id":"ENSG00000172155.9","gene_symbol":"LCE1D","gene_name":"late cornified envelope 1D [Source:HGNC Symbol;Acc:HGNC:29465]","synonyms":"LEP4","biotype":"protein_coding","ncbi_id":"353134","summary":null,"start":152796751,"end":152798181,"strand":1,"description":"late cornified envelope 1D [Source:HGNC Symbol;Acc:HGNC:29465]"}, {"versioned_ensembl_gene_id":"ENSG00000175643.8","gene_symbol":"RMI2","gene_name":"RecQ mediated genome instability 2 [Source:HGNC Symbol;Acc:HGNC:28349]","synonyms":"MGC24665,C16orf75,BLAP18","biotype":"protein_coding","ncbi_id":"116028","summary":"RMI2 is a component of the BLM (RECQL3; MIM 604610) complex, which plays a role in homologous recombination-dependent DNA repair and is essential for genome stability (Xu et al., 2008 [PubMed 18923082]).[supplied by OMIM, Nov 2008]","start":11249619,"end":11351762,"strand":1,"description":"RecQ mediated genome instability 2 [Source:HGNC Symbol;Acc:HGNC:28349]"}, {"versioned_ensembl_gene_id":"ENSG00000197084.5","gene_symbol":"LCE1C","gene_name":"late cornified envelope 1C [Source:HGNC Symbol;Acc:HGNC:29464]","synonyms":"LEP3","biotype":"protein_coding","ncbi_id":"353133","summary":null,"start":152804835,"end":152806628,"strand":-1,"description":"late cornified envelope 1C [Source:HGNC Symbol;Acc:HGNC:29464]"}, {"versioned_ensembl_gene_id":"ENSG00000254687.1","gene_symbol":"AC009646.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":53177571,"end":53242683,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281883.1","gene_symbol":"AL512506.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":43883800,"end":44028526,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000175646.3","gene_symbol":"PRM1","gene_name":"protamine 1 [Source:HGNC Symbol;Acc:HGNC:9447]","synonyms":"CT94.1","biotype":"protein_coding","ncbi_id":"5619","summary":null,"start":11280836,"end":11281350,"strand":-1,"description":"protamine 1 [Source:HGNC Symbol;Acc:HGNC:9447]"}, {"versioned_ensembl_gene_id":"ENSG00000256287.1","gene_symbol":"LINC02398","gene_name":"long intergenic non-protein coding RNA 2398 [Source:HGNC Symbol;Acc:HGNC:53325]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100506393","summary":null,"start":20014780,"end":20098868,"strand":1,"description":"long intergenic non-protein coding RNA 2398 [Source:HGNC Symbol;Acc:HGNC:53325]"}, {"versioned_ensembl_gene_id":"ENSG00000180881.19","gene_symbol":"CAPS2","gene_name":"calcyphosine 2 [Source:HGNC Symbol;Acc:HGNC:16471]","synonyms":null,"biotype":"protein_coding","ncbi_id":"84698","summary":"Calcyphosine-2 is a calcium-binding protein with 2 EF-hand motifs (Wang et al., 2002 [PubMed 11846421]).[supplied by OMIM, Mar 2008]","start":75275979,"end":75390928,"strand":-1,"description":"calcyphosine 2 [Source:HGNC Symbol;Acc:HGNC:16471]"}, {"versioned_ensembl_gene_id":"ENSG00000179630.10","gene_symbol":"LACC1","gene_name":"laccase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26789]","synonyms":"FLJ38725,FAMIN,C13orf31","biotype":"protein_coding","ncbi_id":"144811","summary":"This gene encodes an oxidoreductase that promotes fatty-acid oxidation, with concomitant inflammasome activation, mitochondrial and NADPH-oxidase-dependent reactive oxygen species production, and bactericidal activity of macrophages. The encoded protein forms a complex with fatty acid synthase on peroxisomes and is thought to be modulated by peroxisome proliferator-activated receptor signaling events. Naturally occurring mutations in this gene are associated with inflammatory bowel disease, Behcet's disease, leprosy, ulcerative colitis, early-onset Crohn's disease, and systemic juvenile idiopathic arthritis. [provided by RefSeq, Apr 2017]","start":43879284,"end":43893932,"strand":1,"description":"laccase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:26789]"}, {"versioned_ensembl_gene_id":"ENSG00000215835.2","gene_symbol":"AL596087.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":166275629,"end":166277597,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000233867.2","gene_symbol":"SLC9B1P3","gene_name":"solute carrier family 9 member B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43582]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100421008","summary":null,"start":38640971,"end":38689068,"strand":-1,"description":"solute carrier family 9 member B1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43582]"}, {"versioned_ensembl_gene_id":"ENSG00000256499.1","gene_symbol":"LINC02468","gene_name":"long intergenic non-protein coding RNA 2468 [Source:HGNC Symbol;Acc:HGNC:53406]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105369684","summary":null,"start":20120980,"end":20129813,"strand":-1,"description":"long intergenic non-protein coding RNA 2468 [Source:HGNC Symbol;Acc:HGNC:53406]"}, {"versioned_ensembl_gene_id":"ENSG00000229588.1","gene_symbol":"AL390115.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166334884,"end":166335762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000225325.1","gene_symbol":"AL583804.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":166387727,"end":166452632,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185338.4","gene_symbol":"SOCS1","gene_name":"suppressor of cytokine signaling 1 [Source:HGNC Symbol;Acc:HGNC:19383]","synonyms":"TIP3,SSI-1,SOCS-1,JAB,Cish1","biotype":"protein_coding","ncbi_id":"8651","summary":"This gene encodes a member of the STAT-induced STAT inhibitor (SSI), also known as suppressor of cytokine signaling (SOCS), family. SSI family members are cytokine-inducible negative regulators of cytokine signaling. The expression of this gene can be induced by a subset of cytokines, including IL2, IL3 erythropoietin (EPO), CSF2/GM-CSF, and interferon (IFN)-gamma. The protein encoded by this gene functions downstream of cytokine receptors, and takes part in a negative feedback loop to attenuate cytokine signaling. Knockout studies in mice suggested the role of this gene as a modulator of IFN-gamma action, which is required for normal postnatal growth and survival. [provided by RefSeq, Jul 2008]","start":11254405,"end":11256179,"strand":-1,"description":"suppressor of cytokine signaling 1 [Source:HGNC Symbol;Acc:HGNC:19383]"}, {"versioned_ensembl_gene_id":"ENSG00000164610.8","gene_symbol":"RP9","gene_name":"retinitis pigmentosa 9 (autosomal dominant) [Source:HGNC Symbol;Acc:HGNC:10288]","synonyms":"PAP-1","biotype":"protein_coding","ncbi_id":"6100","summary":"The protein encoded by this gene can be bound and phosphorylated by the protooncogene PIM1 product, a serine/threonine protein kinase . This protein localizes in nuclear speckles containing the splicing factors, and has a role in pre-mRNA splicing. CBF1-interacting protein (CIR), a corepressor of CBF1, can also bind to this protein and effects alternative splicing. Mutations in this gene result in autosomal dominant retinitis pigmentosa-9. This gene has a pseudogene (GeneID: 441212), which is located in tandem array approximately 166 kb distal to this gene. [provided by RefSeq, Sep 2009]","start":33094797,"end":33109401,"strand":-1,"description":"retinitis pigmentosa 9 (autosomal dominant) [Source:HGNC Symbol;Acc:HGNC:10288]"}, {"versioned_ensembl_gene_id":"ENSG00000234142.1","gene_symbol":"LINC01675","gene_name":"long intergenic non-protein coding RNA 1675 [Source:HGNC Symbol;Acc:HGNC:52463]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371590","summary":null,"start":166475772,"end":166490039,"strand":-1,"description":"long intergenic non-protein coding RNA 1675 [Source:HGNC Symbol;Acc:HGNC:52463]"}, {"versioned_ensembl_gene_id":"ENSG00000230231.1","gene_symbol":"FMO7P","gene_name":"flavin containing monooxygenase 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:32208]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100337589","summary":null,"start":166474745,"end":166481565,"strand":1,"description":"flavin containing monooxygenase 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:32208]"}, {"versioned_ensembl_gene_id":"ENSG00000279997.1","gene_symbol":"AC133485.6","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":32185624,"end":32186311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000122304.10","gene_symbol":"PRM2","gene_name":"protamine 2 [Source:HGNC Symbol;Acc:HGNC:9448]","synonyms":"CT94.2","biotype":"protein_coding","ncbi_id":"5620","summary":"Protamines substitute for histones in the chromatin of sperm during the haploid phase of spermatogenesis, and are the major DNA-binding proteins in the nucleus of sperm in many vertebrates. They package the sperm DNA into a highly condensed complex in a volume less than 5% of a somatic cell nucleus. Many mammalian species have only one protamine (protamine 1); however, a few species, including human and mouse, have two. This gene encodes protamine 2, which is cleaved to give rise to a family of protamine 2 peptides. Alternatively spliced transcript variants have also been found for this gene. [provided by RefSeq, Sep 2015]","start":11275639,"end":11276480,"strand":-1,"description":"protamine 2 [Source:HGNC Symbol;Acc:HGNC:9448]"}, {"versioned_ensembl_gene_id":"ENSG00000260584.1","gene_symbol":"AC142381.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":32116700,"end":32116997,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000274001.1","gene_symbol":"AL512506.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":43877715,"end":43878163,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000230267.7","gene_symbol":"HERC2P4","gene_name":"hect domain and RLD 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4872]","synonyms":"D16F37S5","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100289574","summary":null,"start":32103245,"end":32188107,"strand":-1,"description":"hect domain and RLD 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:4872]"}, {"versioned_ensembl_gene_id":"ENSG00000280060.1","gene_symbol":"AL512506.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":43894725,"end":43895182,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000115421.12","gene_symbol":"PAPOLG","gene_name":"poly(A) polymerase gamma [Source:HGNC Symbol;Acc:HGNC:14982]","synonyms":"FLJ12972","biotype":"protein_coding","ncbi_id":"64895","summary":"This gene encodes a member of the poly(A) polymerase family which catalyzes template-independent extension of the 3' end of a DNA/RNA strand. This enzyme shares 60% identity to the well characterized poly(A) polymerase II (PAPII) at the amino acid level. These two enzymes have similar organization of structural and functional domains. This enzyme is exclusively localized in the nucleus and exhibits both nonspecific and CPSF (cleavage and polyadenylation specificity factor)/AAUAAA-dependent polyadenylation activity. This gene is located on chromosome 2 in contrast to the PAPII gene, which is located on chromosome 14. [provided by RefSeq, Jul 2008]","start":60756230,"end":60802085,"strand":1,"description":"poly(A) polymerase gamma [Source:HGNC Symbol;Acc:HGNC:14982]"}, {"versioned_ensembl_gene_id":"ENSG00000227538.1","gene_symbol":"HNRNPFP1","gene_name":"heterogeneous nuclear ribonucleoprotein F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48812]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644449","summary":null,"start":42040597,"end":42041729,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein F pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:48812]"}, {"versioned_ensembl_gene_id":"ENSG00000273987.1","gene_symbol":"AC121761.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":75333798,"end":75334486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000254451.2","gene_symbol":"AC091534.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75234740,"end":75298508,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000228776.2","gene_symbol":"AC114492.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42140635,"end":42141391,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000259353.1","gene_symbol":"AC090515.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":58856831,"end":58865063,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241640.2","gene_symbol":"AC092757.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":59049399,"end":59050385,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000044012.3","gene_symbol":"GUCA2B","gene_name":"guanylate cyclase activator 2B [Source:HGNC Symbol;Acc:HGNC:4683]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2981","summary":"This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products, including uroguanylin, a member of the guanylin family of peptides and an endogenous ligand of the guanylate cyclase-C receptor. Binding of this peptide to its cognate receptor stimulates an increase in cyclic GMP and may regulate salt and water homeostasis in the intestine and kidneys. [provided by RefSeq, Nov 2015]","start":42153421,"end":42155824,"strand":1,"description":"guanylate cyclase activator 2B [Source:HGNC Symbol;Acc:HGNC:4683]"}, {"versioned_ensembl_gene_id":"ENSG00000214725.8","gene_symbol":"CDIPT-AS1","gene_name":"CDIPT antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48609]","synonyms":null,"biotype":"transcribed_unitary_pseudogene","ncbi_id":"440356","summary":null,"start":29863593,"end":29868053,"strand":1,"description":"CDIPT antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:48609]"}, {"versioned_ensembl_gene_id":"ENSG00000281706.2","gene_symbol":"LINC01012","gene_name":"long intergenic non-protein coding RNA 1012 [Source:NCBI gene;Acc:100507173]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100507173","summary":null,"start":27694035,"end":27710222,"strand":1,"description":"long intergenic non-protein coding RNA 1012 [Source:NCBI gene;Acc:100507173]"}, {"versioned_ensembl_gene_id":"ENSG00000269694.1","gene_symbol":"AC005197.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18881680,"end":18883376,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000003402.19","gene_symbol":"CFLAR","gene_name":"CASP8 and FADD like apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:1876]","synonyms":"MRIT,I-FLICE,FLIP,FLAME,CLARP,Casper,CASP8AP1,CASH,c-FLIP","biotype":"protein_coding","ncbi_id":"8837","summary":"The protein encoded by this gene is a regulator of apoptosis and is structurally similar to caspase-8. However, the encoded protein lacks caspase activity and appears to be itself cleaved into two peptides by caspase-8. Several transcript variants encoding different isoforms have been found for this gene, and partial evidence for several more variants exists. [provided by RefSeq, Feb 2011]","start":201116104,"end":201176687,"strand":1,"description":"CASP8 and FADD like apoptosis regulator [Source:HGNC Symbol;Acc:HGNC:1876]"}, {"versioned_ensembl_gene_id":"ENSG00000262603.5","gene_symbol":"AC003958.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":41409741,"end":41432374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000130283.8","gene_symbol":"GDF1","gene_name":"growth differentiation factor 1 [Source:HGNC Symbol;Acc:HGNC:4214]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2657","summary":"This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. Studies in rodents suggest that this protein is involved in the establishment of left-right asymmetry in early embryogenesis and in neural development in later embryogenesis. The encoded protein is translated from a bicistronic mRNA that also encodes ceramide synthase 1. Mutations in this gene are associated with several congenital cardiovascular malformations. [provided by RefSeq, Jul 2016]","start":18868545,"end":18896096,"strand":-1,"description":"growth differentiation factor 1 [Source:HGNC Symbol;Acc:HGNC:4214]"}, {"versioned_ensembl_gene_id":"ENSG00000137776.16","gene_symbol":"SLTM","gene_name":"SAFB like transcription modulator [Source:HGNC Symbol;Acc:HGNC:20709]","synonyms":"Met,FLJ13213","biotype":"protein_coding","ncbi_id":"79811","summary":null,"start":58879045,"end":58933653,"strand":-1,"description":"SAFB like transcription modulator [Source:HGNC Symbol;Acc:HGNC:20709]"}, {"versioned_ensembl_gene_id":"ENSG00000262040.1","gene_symbol":"AC003958.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":41413837,"end":41419100,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000263022.1","gene_symbol":"KRT37","gene_name":"keratin 37 [Source:HGNC Symbol;Acc:HGNC:6455]","synonyms":"KRTHA7","biotype":"protein_coding","ncbi_id":"8688","summary":"The protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription. [provided by RefSeq, Jul 2008]","start":41428078,"end":41431848,"strand":-1,"description":"keratin 37 [Source:HGNC Symbol;Acc:HGNC:6455]"}, {"versioned_ensembl_gene_id":"ENSG00000235308.1","gene_symbol":"AL445991.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":88923370,"end":88923844,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253982.1","gene_symbol":"AC100810.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":1761990,"end":1764502,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000056097.15","gene_symbol":"ZFR","gene_name":"zinc finger RNA binding protein [Source:HGNC Symbol;Acc:HGNC:17277]","synonyms":"ZFR1,SPG71","biotype":"protein_coding","ncbi_id":"51663","summary":"This gene encodes an RNA-binding protein characterized by its DZF (domain associated with zinc fingers) domain. The encoded protein may play a role in the nucleocytoplasmic shuttling of another RNA-binding protein, Staufen homolog 2, in neurons. Expression of this gene is regulated through alternative polyadenylation that mediates differential microRNA targeting. Elevated expression of this gene has been observed in human patients with pancreatic cancer and knockdown of this gene may result in reduced viability and invasion of pancreatic cancer cells. [provided by RefSeq, Sep 2016]","start":32354350,"end":32444761,"strand":-1,"description":"zinc finger RNA binding protein [Source:HGNC Symbol;Acc:HGNC:17277]"}, {"versioned_ensembl_gene_id":"ENSG00000216915.2","gene_symbol":"GPR89P","gene_name":"G protein-coupled receptor 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:13951]","synonyms":"C11H1.2-Lp","biotype":"processed_pseudogene","ncbi_id":"394254","summary":null,"start":27737000,"end":27738494,"strand":-1,"description":"G protein-coupled receptor 89 pseudogene [Source:HGNC Symbol;Acc:HGNC:13951]"}, {"versioned_ensembl_gene_id":"ENSG00000237947.1","gene_symbol":"AL583854.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":40713411,"end":40715363,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000227264.3","gene_symbol":"ACTR3BP5","gene_name":"ACTR3B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38682]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"399746","summary":null,"start":38696424,"end":38697902,"strand":1,"description":"ACTR3B pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:38682]"}, {"versioned_ensembl_gene_id":"ENSG00000218069.2","gene_symbol":"RSL24D1P1","gene_name":"ribosomal L24 domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13979]","synonyms":"RSL24D1P,RPL30BP,RPL24p,dJ97D16.2","biotype":"processed_pseudogene","ncbi_id":"100129755","summary":null,"start":27780619,"end":27781111,"strand":-1,"description":"ribosomal L24 domain containing 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:13979]"}, {"versioned_ensembl_gene_id":"ENSG00000283239.1","gene_symbol":"KBTBD11-OT1","gene_name":"KBTBD11 overlapping transcript 1 [Source:NCBI gene;Acc:104266957]","synonyms":null,"biotype":"protein_coding","ncbi_id":"104266957","summary":null,"start":1763888,"end":1958627,"strand":1,"description":"KBTBD11 overlapping transcript 1 [Source:NCBI gene;Acc:104266957]"}, {"versioned_ensembl_gene_id":"ENSG00000217862.2","gene_symbol":"AL009179.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":27807075,"end":27807339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000197273.3","gene_symbol":"GUCA2A","gene_name":"guanylate cyclase activator 2A [Source:HGNC Symbol;Acc:HGNC:4682]","synonyms":"STARA,GUCA2","biotype":"protein_coding","ncbi_id":"2980","summary":null,"start":42162691,"end":42164718,"strand":-1,"description":"guanylate cyclase activator 2A [Source:HGNC Symbol;Acc:HGNC:4682]"}, {"versioned_ensembl_gene_id":"ENSG00000229283.1","gene_symbol":"AL356387.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":111317600,"end":111323981,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000185130.5","gene_symbol":"HIST1H2BL","gene_name":"histone cluster 1 H2B family member l [Source:HGNC Symbol;Acc:HGNC:4748]","synonyms":"H2BFC,H2B/c,dJ97D16.4","biotype":"protein_coding","ncbi_id":"8340","summary":"Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]","start":27807444,"end":27807931,"strand":-1,"description":"histone cluster 1 H2B family member l [Source:HGNC Symbol;Acc:HGNC:4748]"}, {"versioned_ensembl_gene_id":"ENSG00000232240.2","gene_symbol":"AL356387.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":111323833,"end":111324075,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000236356.1","gene_symbol":"AC079584.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":143799467,"end":143819599,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000162783.10","gene_symbol":"IER5","gene_name":"immediate early response 5 [Source:HGNC Symbol;Acc:HGNC:5393]","synonyms":null,"biotype":"protein_coding","ncbi_id":"51278","summary":"This gene encodes a protein that is similar to other immediate early response proteins. In the mouse, a similar gene may play an important role in mediating the cellular response to mitogenic signals. Studies in rats found the expression of a similar gene to be increased after waking and sleep deprivation. [provided by RefSeq, Jul 2008]","start":181088712,"end":181092899,"strand":1,"description":"immediate early response 5 [Source:HGNC Symbol;Acc:HGNC:5393]"}, {"versioned_ensembl_gene_id":"ENSG00000263140.5","gene_symbol":"C21orf62-AS1","gene_name":"C21orf62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1290]","synonyms":"C21orf49","biotype":"antisense_RNA","ncbi_id":"54067","summary":null,"start":32772100,"end":32798969,"strand":1,"description":"C21orf62 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:1290]"}, {"versioned_ensembl_gene_id":"ENSG00000272579.1","gene_symbol":"AL136370.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":193090866,"end":193091556,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000270542.1","gene_symbol":"AL356218.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":33449755,"end":33449941,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000276390.1","gene_symbol":"AC004241.3","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":47699401,"end":47699917,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000252119.1","gene_symbol":"ACA64","gene_name":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":119323293,"end":119323409,"strand":-1,"description":"Small nucleolar RNA ACA64 [Source:RFAM;Acc:RF01225]"}, {"versioned_ensembl_gene_id":"ENSG00000201594.1","gene_symbol":"RNA5SP517","gene_name":"RNA, 5S ribosomal pseudogene 517 [Source:HGNC Symbol;Acc:HGNC:43417]","synonyms":"RN5S517","biotype":"rRNA","ncbi_id":"100873568","summary":null,"start":146427456,"end":146427572,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 517 [Source:HGNC Symbol;Acc:HGNC:43417]"}, {"versioned_ensembl_gene_id":"ENSG00000207695.1","gene_symbol":"MIR184","gene_name":"microRNA 184 [Source:HGNC Symbol;Acc:HGNC:31555]","synonyms":"MIRN184,hsa-mir-184","biotype":"miRNA","ncbi_id":"406960","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of target mRNAs. This microRNA represents the most abundant miRNA in the corneal and lens epithelia of the eye and has been shown to interfere with target binding by another miRNA, miR-205. Through regulation of the VEGF and Akt signaling pathways, this microRNA may inhibit corneal angiogenesis. Mutations in the seed region of this microRNA cause familial keratoconus with cataract, also known as EDICT syndrome. [provided by RefSeq, Mar 2017]","start":79209788,"end":79209871,"strand":1,"description":"microRNA 184 [Source:HGNC Symbol;Acc:HGNC:31555]"}, {"versioned_ensembl_gene_id":"ENSG00000221634.1","gene_symbol":"MIR1276","gene_name":"microRNA 1276 [Source:HGNC Symbol;Acc:HGNC:35347]","synonyms":"MIRN1276,hsa-mir-1276","biotype":"miRNA","ncbi_id":"100302121","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85770496,"end":85770578,"strand":-1,"description":"microRNA 1276 [Source:HGNC Symbol;Acc:HGNC:35347]"}, {"versioned_ensembl_gene_id":"ENSG00000243227.3","gene_symbol":"RN7SL55P","gene_name":"RNA, 7SL, cytoplasmic 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46071]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479244","summary":null,"start":109450772,"end":109451068,"strand":-1,"description":"RNA, 7SL, cytoplasmic 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:46071]"}, {"versioned_ensembl_gene_id":"ENSG00000276366.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":240289216,"end":240289443,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000284346.1","gene_symbol":"MIR940","gene_name":"microRNA 940 [Source:HGNC Symbol;Acc:HGNC:33683]","synonyms":"MIRN940,hsa-mir-940","biotype":"miRNA","ncbi_id":"100126328","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2271747,"end":2271840,"strand":1,"description":"microRNA 940 [Source:HGNC Symbol;Acc:HGNC:33683]"}, {"versioned_ensembl_gene_id":"ENSG00000222439.1","gene_symbol":"RNU6-994P","gene_name":"RNA, U6 small nuclear 994, pseudogene [Source:HGNC Symbol;Acc:HGNC:47957]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480006","summary":null,"start":63337339,"end":63337449,"strand":1,"description":"RNA, U6 small nuclear 994, pseudogene [Source:HGNC Symbol;Acc:HGNC:47957]"}, {"versioned_ensembl_gene_id":"ENSG00000284184.1","gene_symbol":"MIR6506","gene_name":"microRNA 6506 [Source:HGNC Symbol;Acc:HGNC:50158]","synonyms":"hsa-mir-6506","biotype":"miRNA","ncbi_id":"102465252","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15611030,"end":15611095,"strand":-1,"description":"microRNA 6506 [Source:HGNC Symbol;Acc:HGNC:50158]"}, {"versioned_ensembl_gene_id":"ENSG00000264314.1","gene_symbol":"MIR548AT","gene_name":"microRNA 548at [Source:HGNC Symbol;Acc:HGNC:43517]","synonyms":"hsa-mir-548at","biotype":"miRNA","ncbi_id":"100847030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42494773,"end":42494830,"strand":1,"description":"microRNA 548at [Source:HGNC Symbol;Acc:HGNC:43517]"}, {"versioned_ensembl_gene_id":"ENSG00000201491.1","gene_symbol":"RNU4-75P","gene_name":"RNA, U4 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:47011]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479593","summary":null,"start":99784740,"end":99784885,"strand":-1,"description":"RNA, U4 small nuclear 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:47011]"}, {"versioned_ensembl_gene_id":"ENSG00000273929.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868959,"end":54869065,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000266672.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29578848,"end":29578931,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000202063.1","gene_symbol":"RNA5SP79","gene_name":"RNA, 5S ribosomal pseudogene 79 [Source:HGNC Symbol;Acc:HGNC:42856]","synonyms":"RN5S79","biotype":"rRNA","ncbi_id":"100873313","summary":null,"start":230820250,"end":230820358,"strand":1,"description":"RNA, 5S ribosomal pseudogene 79 [Source:HGNC Symbol;Acc:HGNC:42856]"}, {"versioned_ensembl_gene_id":"ENSG00000252807.1","gene_symbol":"RNU6-1006P","gene_name":"RNA, U6 small nuclear 1006, pseudogene [Source:HGNC Symbol;Acc:HGNC:47969]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480010","summary":null,"start":170119996,"end":170120098,"strand":-1,"description":"RNA, U6 small nuclear 1006, pseudogene [Source:HGNC Symbol;Acc:HGNC:47969]"}, {"versioned_ensembl_gene_id":"ENSG00000252959.1","gene_symbol":"RNA5SP170","gene_name":"RNA, 5S ribosomal pseudogene 170 [Source:HGNC Symbol;Acc:HGNC:43070]","synonyms":"RN5S170","biotype":"rRNA","ncbi_id":"100873435","summary":null,"start":166053187,"end":166053287,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 170 [Source:HGNC Symbol;Acc:HGNC:43070]"}, {"versioned_ensembl_gene_id":"ENSG00000278682.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"NBS1,FLJ20510,PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1,CLR19.9","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54703078,"end":54738934,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000283492.1","gene_symbol":"MIR7153","gene_name":"microRNA 7153 [Source:HGNC Symbol;Acc:HGNC:50190]","synonyms":"hsa-mir-7153","biotype":"miRNA","ncbi_id":"102465690","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11654885,"end":11654941,"strand":-1,"description":"microRNA 7153 [Source:HGNC Symbol;Acc:HGNC:50190]"}, {"versioned_ensembl_gene_id":"ENSG00000284553.1","gene_symbol":"MIR6886","gene_name":"microRNA 6886 [Source:HGNC Symbol;Acc:HGNC:50121]","synonyms":"hsa-mir-6886","biotype":"miRNA","ncbi_id":"102465534","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11113474,"end":11113534,"strand":1,"description":"microRNA 6886 [Source:HGNC Symbol;Acc:HGNC:50121]"}, {"versioned_ensembl_gene_id":"ENSG00000223215.1","gene_symbol":"RNU6-607P","gene_name":"RNA, U6 small nuclear 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:47570]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481772","summary":null,"start":37668898,"end":37669005,"strand":1,"description":"RNA, U6 small nuclear 607, pseudogene [Source:HGNC Symbol;Acc:HGNC:47570]"}, {"versioned_ensembl_gene_id":"ENSG00000264175.1","gene_symbol":"MIR3189","gene_name":"microRNA 3189 [Source:HGNC Symbol;Acc:HGNC:38307]","synonyms":"hsa-mir-3189","biotype":"miRNA","ncbi_id":"100422943","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18386562,"end":18386634,"strand":1,"description":"microRNA 3189 [Source:HGNC Symbol;Acc:HGNC:38307]"}, {"versioned_ensembl_gene_id":"ENSG00000252757.1","gene_symbol":"RN7SKP96","gene_name":"RNA, 7SK small nuclear pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:45820]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479137","summary":null,"start":86336318,"end":86336614,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 96 [Source:HGNC Symbol;Acc:HGNC:45820]"}, {"versioned_ensembl_gene_id":"ENSG00000201747.1","gene_symbol":"RNU6-534P","gene_name":"RNA, U6 small nuclear 534, pseudogene [Source:HGNC Symbol;Acc:HGNC:47497]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481978","summary":null,"start":7906519,"end":7906624,"strand":1,"description":"RNA, U6 small nuclear 534, pseudogene [Source:HGNC Symbol;Acc:HGNC:47497]"}, {"versioned_ensembl_gene_id":"ENSG00000264979.1","gene_symbol":"MIR4436B1","gene_name":"microRNA 4436b-1 [Source:HGNC Symbol;Acc:HGNC:41587]","synonyms":"MIR4436B,hsa-mir-4436b","biotype":"miRNA","ncbi_id":"100616123","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110086433,"end":110086523,"strand":-1,"description":"microRNA 4436b-1 [Source:HGNC Symbol;Acc:HGNC:41587]"}, {"versioned_ensembl_gene_id":"ENSG00000263973.1","gene_symbol":"MIR4760","gene_name":"microRNA 4760 [Source:HGNC Symbol;Acc:HGNC:41698]","synonyms":"hsa-mir-4760","biotype":"miRNA","ncbi_id":"100616148","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40212352,"end":40212431,"strand":-1,"description":"microRNA 4760 [Source:HGNC Symbol;Acc:HGNC:41698]"}, {"versioned_ensembl_gene_id":"ENSG00000266329.1","gene_symbol":"MIR4281","gene_name":"microRNA 4281 [Source:HGNC Symbol;Acc:HGNC:38357]","synonyms":"hsa-mir-4281","biotype":"miRNA","ncbi_id":"100422962","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176629439,"end":176629500,"strand":-1,"description":"microRNA 4281 [Source:HGNC Symbol;Acc:HGNC:38357]"}, {"versioned_ensembl_gene_id":"ENSG00000252081.1","gene_symbol":"RNU6-277P","gene_name":"RNA, U6 small nuclear 277, pseudogene [Source:HGNC Symbol;Acc:HGNC:47240]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481266","summary":null,"start":105974826,"end":105974931,"strand":-1,"description":"RNA, U6 small nuclear 277, pseudogene [Source:HGNC Symbol;Acc:HGNC:47240]"}, {"versioned_ensembl_gene_id":"ENSG00000265724.1","gene_symbol":"MIR4284","gene_name":"microRNA 4284 [Source:HGNC Symbol;Acc:HGNC:38322]","synonyms":"hsa-mir-4284","biotype":"miRNA","ncbi_id":"100422948","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":73711317,"end":73711397,"strand":1,"description":"microRNA 4284 [Source:HGNC Symbol;Acc:HGNC:38322]"}, {"versioned_ensembl_gene_id":"ENSG00000199801.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69985986,"end":69986094,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207597.1","gene_symbol":"MIR490","gene_name":"microRNA 490 [Source:HGNC Symbol;Acc:HGNC:32075]","synonyms":"MIRN490,miR-490,hsa-mir-490","biotype":"miRNA","ncbi_id":"574443","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136903167,"end":136903294,"strand":1,"description":"microRNA 490 [Source:HGNC Symbol;Acc:HGNC:32075]"}, {"versioned_ensembl_gene_id":"ENSG00000273694.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":120571120,"end":120571264,"strand":1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000265465.1","gene_symbol":"MIR4768","gene_name":"microRNA 4768 [Source:HGNC Symbol;Acc:HGNC:41592]","synonyms":"hsa-mir-4768","biotype":"miRNA","ncbi_id":"100616249","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17425881,"end":17425954,"strand":1,"description":"microRNA 4768 [Source:HGNC Symbol;Acc:HGNC:41592]"}, {"versioned_ensembl_gene_id":"ENSG00000207008.1","gene_symbol":"SNORA54","gene_name":"small nucleolar RNA, H/ACA box 54 [Source:HGNC Symbol;Acc:HGNC:32647]","synonyms":"ACA54,ACA54","biotype":"snoRNA","ncbi_id":"677833","summary":null,"start":2963771,"end":2963893,"strand":-1,"description":"small nucleolar RNA, H/ACA box 54 [Source:HGNC Symbol;Acc:HGNC:32647]"}, {"versioned_ensembl_gene_id":"ENSG00000265392.1","gene_symbol":"MIR4252","gene_name":"microRNA 4252 [Source:HGNC Symbol;Acc:HGNC:38384]","synonyms":"hsa-mir-4252","biotype":"miRNA","ncbi_id":"100422975","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6429834,"end":6429896,"strand":-1,"description":"microRNA 4252 [Source:HGNC Symbol;Acc:HGNC:38384]"}, {"versioned_ensembl_gene_id":"ENSG00000252577.1","gene_symbol":"SCARNA20","gene_name":"small Cajal body-specific RNA 20 [Source:HGNC Symbol;Acc:HGNC:32578]","synonyms":"ACA66","biotype":"scaRNA","ncbi_id":"677681","summary":null,"start":60231516,"end":60231646,"strand":-1,"description":"small Cajal body-specific RNA 20 [Source:HGNC Symbol;Acc:HGNC:32578]"}, {"versioned_ensembl_gene_id":"ENSG00000277027.1","gene_symbol":"RMRP","gene_name":"RNA component of mitochondrial RNA processing endoribonuclease [Source:HGNC Symbol;Acc:HGNC:10031]","synonyms":"RMRPR,RRP2,NME1,RMRPR,CHH,NME1,CHH,RRP2","biotype":"ribozyme","ncbi_id":"6023","summary":"This gene encodes the RNA component of mitochondrial RNA processing endoribonuclease, which cleaves mitochondrial RNA at a priming site of mitochondrial DNA replication. This RNA also interacts with the telomerase reverse transcriptase catalytic subunit to form a distinct ribonucleoprotein complex that has RNA-dependent RNA polymerase activity and produces double-stranded RNAs that can be processed into small interfering RNA. Mutations in this gene are associated with cartilage-hair hypoplasia.[provided by RefSeq, Mar 2010]","start":35657754,"end":35658017,"strand":-1,"description":"RNA component of mitochondrial RNA processing endoribonuclease [Source:HGNC Symbol;Acc:HGNC:10031]"}, {"versioned_ensembl_gene_id":"ENSG00000239211.3","gene_symbol":"RN7SL563P","gene_name":"RNA, 7SL, cytoplasmic 563, pseudogene [Source:HGNC Symbol;Acc:HGNC:46579]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479427","summary":null,"start":101397636,"end":101397933,"strand":-1,"description":"RNA, 7SL, cytoplasmic 563, pseudogene [Source:HGNC Symbol;Acc:HGNC:46579]"}, {"versioned_ensembl_gene_id":"ENSG00000283920.1","gene_symbol":"MIR6743","gene_name":"microRNA 6743 [Source:HGNC Symbol;Acc:HGNC:50008]","synonyms":"hsa-mir-6743","biotype":"miRNA","ncbi_id":"102465445","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":209336,"end":209406,"strand":1,"description":"microRNA 6743 [Source:HGNC Symbol;Acc:HGNC:50008]"}, {"versioned_ensembl_gene_id":"ENSG00000207800.3","gene_symbol":"MIR504","gene_name":"microRNA 504 [Source:HGNC Symbol;Acc:HGNC:32139]","synonyms":"MIRN504,hsa-mir-504","biotype":"miRNA","ncbi_id":"574507","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":138667711,"end":138667793,"strand":-1,"description":"microRNA 504 [Source:HGNC Symbol;Acc:HGNC:32139]"}, {"versioned_ensembl_gene_id":"ENSG00000265744.1","gene_symbol":"MIR4427","gene_name":"microRNA 4427 [Source:HGNC Symbol;Acc:HGNC:41678]","synonyms":"hsa-mir-4427","biotype":"miRNA","ncbi_id":"100616390","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":233624152,"end":233624219,"strand":1,"description":"microRNA 4427 [Source:HGNC Symbol;Acc:HGNC:41678]"}, {"versioned_ensembl_gene_id":"ENSG00000223012.1","gene_symbol":"RN7SKP264","gene_name":"RNA, 7SK small nuclear pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:45988]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479213","summary":null,"start":86258358,"end":86258646,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 264 [Source:HGNC Symbol;Acc:HGNC:45988]"}, {"versioned_ensembl_gene_id":"ENSG00000266719.1","gene_symbol":"MIR4676","gene_name":"microRNA 4676 [Source:HGNC Symbol;Acc:HGNC:41691]","synonyms":"hsa-mir-4676","biotype":"miRNA","ncbi_id":"100616286","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72721029,"end":72721100,"strand":1,"description":"microRNA 4676 [Source:HGNC Symbol;Acc:HGNC:41691]"}, {"versioned_ensembl_gene_id":"ENSG00000241420.3","gene_symbol":"RN7SL505P","gene_name":"RNA, 7SL, cytoplasmic 505, pseudogene [Source:HGNC Symbol;Acc:HGNC:46521]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481758","summary":null,"start":33045798,"end":33046090,"strand":-1,"description":"RNA, 7SL, cytoplasmic 505, pseudogene [Source:HGNC Symbol;Acc:HGNC:46521]"}, {"versioned_ensembl_gene_id":"ENSG00000221703.1","gene_symbol":"MIR302E","gene_name":"microRNA 302e [Source:HGNC Symbol;Acc:HGNC:35348]","synonyms":"hsa-mir-302e,MIRN302E","biotype":"miRNA","ncbi_id":"100313774","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7234766,"end":7234837,"strand":1,"description":"microRNA 302e [Source:HGNC Symbol;Acc:HGNC:35348]"}, {"versioned_ensembl_gene_id":"ENSG00000201955.1","gene_symbol":"RNY3P1","gene_name":"RNA, Ro-associated Y3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42477]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106478984","summary":null,"start":79170234,"end":79170335,"strand":-1,"description":"RNA, Ro-associated Y3 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42477]"}, {"versioned_ensembl_gene_id":"ENSG00000284415.1","gene_symbol":"MIR1287","gene_name":"microRNA 1287 [Source:HGNC Symbol;Acc:HGNC:35280]","synonyms":"MIRN1287,hsa-mir-1287","biotype":"miRNA","ncbi_id":"100302133","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98395218,"end":98395307,"strand":-1,"description":"microRNA 1287 [Source:HGNC Symbol;Acc:HGNC:35280]"}, {"versioned_ensembl_gene_id":"ENSG00000264603.1","gene_symbol":"MIR3159","gene_name":"microRNA 3159 [Source:HGNC Symbol;Acc:HGNC:38181]","synonyms":"hsa-mir-3159","biotype":"miRNA","ncbi_id":"100423016","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18387787,"end":18387860,"strand":1,"description":"microRNA 3159 [Source:HGNC Symbol;Acc:HGNC:38181]"}, {"versioned_ensembl_gene_id":"ENSG00000274986.1","gene_symbol":"MIR6750","gene_name":"microRNA 6750 [Source:HGNC Symbol;Acc:HGNC:49965]","synonyms":"hsa-mir-6750","biotype":"miRNA","ncbi_id":"102466192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64898363,"end":64898437,"strand":-1,"description":"microRNA 6750 [Source:HGNC Symbol;Acc:HGNC:49965]"}, {"versioned_ensembl_gene_id":"ENSG00000251983.1","gene_symbol":"RN7SKP157","gene_name":"RNA, 7SK small nuclear pseudogene 157 [Source:HGNC Symbol;Acc:HGNC:45881]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479165","summary":null,"start":62146665,"end":62146946,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 157 [Source:HGNC Symbol;Acc:HGNC:45881]"}, {"versioned_ensembl_gene_id":"ENSG00000239547.3","gene_symbol":"RN7SL843P","gene_name":"RNA, 7SL, cytoplasmic 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:46859]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481151","summary":null,"start":17352881,"end":17353177,"strand":-1,"description":"RNA, 7SL, cytoplasmic 843, pseudogene [Source:HGNC Symbol;Acc:HGNC:46859]"}, {"versioned_ensembl_gene_id":"ENSG00000202119.1","gene_symbol":"RNU6-302P","gene_name":"RNA, U6 small nuclear 302, pseudogene [Source:HGNC Symbol;Acc:HGNC:47265]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479701","summary":null,"start":150939222,"end":150939328,"strand":1,"description":"RNA, U6 small nuclear 302, pseudogene [Source:HGNC Symbol;Acc:HGNC:47265]"}, {"versioned_ensembl_gene_id":"ENSG00000263615.1","gene_symbol":"MIR4306","gene_name":"microRNA 4306 [Source:HGNC Symbol;Acc:HGNC:38350]","synonyms":"hsa-mir-4306","biotype":"miRNA","ncbi_id":"100422861","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":99643059,"end":99643149,"strand":1,"description":"microRNA 4306 [Source:HGNC Symbol;Acc:HGNC:38350]"}, {"versioned_ensembl_gene_id":"ENSG00000266215.1","gene_symbol":"MIR3167","gene_name":"microRNA 3167 [Source:HGNC Symbol;Acc:HGNC:38242]","synonyms":"hsa-mir-3167","biotype":"miRNA","ncbi_id":"100422918","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":126988458,"end":126988542,"strand":-1,"description":"microRNA 3167 [Source:HGNC Symbol;Acc:HGNC:38242]"}, {"versioned_ensembl_gene_id":"ENSG00000252494.1","gene_symbol":"RNU6-126P","gene_name":"RNA, U6 small nuclear 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:47089]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479622","summary":null,"start":78133420,"end":78133522,"strand":-1,"description":"RNA, U6 small nuclear 126, pseudogene [Source:HGNC Symbol;Acc:HGNC:47089]"}, {"versioned_ensembl_gene_id":"ENSG00000266461.1","gene_symbol":"MIR2392","gene_name":"microRNA 2392 [Source:HGNC Symbol;Acc:HGNC:41843]","synonyms":"hsa-mir-2392","biotype":"miRNA","ncbi_id":"100616495","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100814491,"end":100814574,"strand":1,"description":"microRNA 2392 [Source:HGNC Symbol;Acc:HGNC:41843]"}, {"versioned_ensembl_gene_id":"ENSG00000273986.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36561237,"end":36561530,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201643.1","gene_symbol":"SNORA14A","gene_name":"small nucleolar RNA, H/ACA box 14A [Source:HGNC Symbol;Acc:HGNC:32602]","synonyms":"ACA14a","biotype":"snoRNA","ncbi_id":"677801","summary":"Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 1. [provided by RefSeq, Oct 2008]","start":75943782,"end":75943916,"strand":1,"description":"small nucleolar RNA, H/ACA box 14A [Source:HGNC Symbol;Acc:HGNC:32602]"}, {"versioned_ensembl_gene_id":"ENSG00000207983.1","gene_symbol":"MIR613","gene_name":"microRNA 613 [Source:HGNC Symbol;Acc:HGNC:32869]","synonyms":"MIRN613,hsa-mir-613","biotype":"miRNA","ncbi_id":"693198","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12764649,"end":12764743,"strand":1,"description":"microRNA 613 [Source:HGNC Symbol;Acc:HGNC:32869]"}, {"versioned_ensembl_gene_id":"ENSG00000283484.1","gene_symbol":"MIR3529","gene_name":"microRNA 3529 [Source:HGNC Symbol;Acc:HGNC:41564]","synonyms":"hsa-mir-3529","biotype":"miRNA","ncbi_id":"100616238","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88611847,"end":88611924,"strand":-1,"description":"microRNA 3529 [Source:HGNC Symbol;Acc:HGNC:41564]"}, {"versioned_ensembl_gene_id":"ENSG00000201591.1","gene_symbol":"RNU6-99P","gene_name":"RNA, U6 small nuclear 99, pseudogene [Source:HGNC Symbol;Acc:HGNC:47062]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479610","summary":null,"start":39261107,"end":39261213,"strand":1,"description":"RNA, U6 small nuclear 99, pseudogene [Source:HGNC Symbol;Acc:HGNC:47062]"}, {"versioned_ensembl_gene_id":"ENSG00000276213.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":152025194,"end":152025472,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266204.1","gene_symbol":"MIR5589","gene_name":"microRNA 5589 [Source:HGNC Symbol;Acc:HGNC:43514]","synonyms":"hsa-mir-5589","biotype":"miRNA","ncbi_id":"100847093","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10038354,"end":10038413,"strand":1,"description":"microRNA 5589 [Source:HGNC Symbol;Acc:HGNC:43514]"}, {"versioned_ensembl_gene_id":"ENSG00000208028.1","gene_symbol":"MIR616","gene_name":"microRNA 616 [Source:HGNC Symbol;Acc:HGNC:32872]","synonyms":"MIRN616,hsa-mir-616","biotype":"miRNA","ncbi_id":"693201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57519163,"end":57519259,"strand":-1,"description":"microRNA 616 [Source:HGNC Symbol;Acc:HGNC:32872]"}, {"versioned_ensembl_gene_id":"ENSG00000221241.1","gene_symbol":"SNORD88A","gene_name":"small nucleolar RNA, C/D box 88A [Source:HGNC Symbol;Acc:HGNC:32747]","synonyms":"HBII-180A","biotype":"snoRNA","ncbi_id":"692202","summary":null,"start":50799442,"end":50799532,"strand":-1,"description":"small nucleolar RNA, C/D box 88A [Source:HGNC Symbol;Acc:HGNC:32747]"}, {"versioned_ensembl_gene_id":"ENSG00000200175.1","gene_symbol":"RNU6-1309P","gene_name":"RNA, U6 small nuclear 1309, pseudogene [Source:HGNC Symbol;Acc:HGNC:48272]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480410","summary":null,"start":150812591,"end":150812698,"strand":-1,"description":"RNA, U6 small nuclear 1309, pseudogene [Source:HGNC Symbol;Acc:HGNC:48272]"}, {"versioned_ensembl_gene_id":"ENSG00000207706.1","gene_symbol":"MIR518F","gene_name":"microRNA 518f [Source:HGNC Symbol;Acc:HGNC:32104]","synonyms":"MIRN518F,hsa-mir-518f","biotype":"miRNA","ncbi_id":"574472","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53700015,"end":53700101,"strand":1,"description":"microRNA 518f [Source:HGNC Symbol;Acc:HGNC:32104]"}, {"versioned_ensembl_gene_id":"ENSG00000201574.1","gene_symbol":"RNU1-93P","gene_name":"RNA, U1 small nuclear 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:48435]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480180","summary":null,"start":231133462,"end":231133630,"strand":1,"description":"RNA, U1 small nuclear 93, pseudogene [Source:HGNC Symbol;Acc:HGNC:48435]"}, {"versioned_ensembl_gene_id":"ENSG00000222320.1","gene_symbol":"RNU6-1050P","gene_name":"RNA, U6 small nuclear 1050, pseudogene [Source:HGNC Symbol;Acc:HGNC:48013]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481512","summary":null,"start":31937533,"end":31937639,"strand":1,"description":"RNA, U6 small nuclear 1050, pseudogene [Source:HGNC Symbol;Acc:HGNC:48013]"}, {"versioned_ensembl_gene_id":"ENSG00000222335.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":196202349,"end":196202453,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243541.3","gene_symbol":"RN7SL104P","gene_name":"RNA, 7SL, cytoplasmic 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:46120]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480949","summary":null,"start":15950689,"end":15950981,"strand":-1,"description":"RNA, 7SL, cytoplasmic 104, pseudogene [Source:HGNC Symbol;Acc:HGNC:46120]"}, {"versioned_ensembl_gene_id":"ENSG00000202211.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43247680,"end":43247781,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199172.3","gene_symbol":"MIR331","gene_name":"microRNA 331 [Source:HGNC Symbol;Acc:HGNC:31772]","synonyms":"MIRN331,hsa-mir-331","biotype":"miRNA","ncbi_id":"442903","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95308420,"end":95308513,"strand":1,"description":"microRNA 331 [Source:HGNC Symbol;Acc:HGNC:31772]"}, {"versioned_ensembl_gene_id":"ENSG00000263909.1","gene_symbol":"MIR5000","gene_name":"microRNA 5000 [Source:HGNC Symbol;Acc:HGNC:43464]","synonyms":"hsa-mir-5000","biotype":"miRNA","ncbi_id":"100846995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75090812,"end":75090914,"strand":1,"description":"microRNA 5000 [Source:HGNC Symbol;Acc:HGNC:43464]"}, {"versioned_ensembl_gene_id":"ENSG00000200745.1","gene_symbol":"RNU1-31P","gene_name":"RNA, U1 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:48373]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481606","summary":null,"start":236210373,"end":236210548,"strand":-1,"description":"RNA, U1 small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:48373]"}, {"versioned_ensembl_gene_id":"ENSG00000201285.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":148008100,"end":148008215,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000281863.1","gene_symbol":"SNORA43","gene_name":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":8931495,"end":8931632,"strand":1,"description":"Small nucleolar RNA SNORA43 [Source:RFAM;Acc:RF00416]"}, {"versioned_ensembl_gene_id":"ENSG00000207652.1","gene_symbol":"MIR621","gene_name":"microRNA 621 [Source:HGNC Symbol;Acc:HGNC:32877]","synonyms":"MIRN621,hsa-mir-621","biotype":"miRNA","ncbi_id":"693206","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40810766,"end":40810861,"strand":1,"description":"microRNA 621 [Source:HGNC Symbol;Acc:HGNC:32877]"}, {"versioned_ensembl_gene_id":"ENSG00000263813.1","gene_symbol":"MIR3679","gene_name":"microRNA 3679 [Source:HGNC Symbol;Acc:HGNC:38979]","synonyms":"hsa-mir-3679","biotype":"miRNA","ncbi_id":"100500878","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134127125,"end":134127192,"strand":1,"description":"microRNA 3679 [Source:HGNC Symbol;Acc:HGNC:38979]"}, {"versioned_ensembl_gene_id":"ENSG00000202233.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":25264656,"end":25264882,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000252188.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":138625060,"end":138625179,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000275453.2","gene_symbol":"MIR548O2","gene_name":"microRNA 548o-2 [Source:HGNC Symbol;Acc:HGNC:41882]","synonyms":"hsa-mir-548o-2","biotype":"miRNA","ncbi_id":"100616190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38516563,"end":38516632,"strand":1,"description":"microRNA 548o-2 [Source:HGNC Symbol;Acc:HGNC:41882]"}, {"versioned_ensembl_gene_id":"ENSG00000201962.1","gene_symbol":"RNA5SP126","gene_name":"RNA, 5S ribosomal pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:43026]","synonyms":"RN5S126","biotype":"rRNA","ncbi_id":"100873396","summary":null,"start":25352284,"end":25352392,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 126 [Source:HGNC Symbol;Acc:HGNC:43026]"}, {"versioned_ensembl_gene_id":"ENSG00000212428.1","gene_symbol":"SNORD115","gene_name":"Small nucleolar RNA SNORD115 [Source:RFAM;Acc:RF00105]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":25159221,"end":25159279,"strand":1,"description":"Small nucleolar RNA SNORD115 [Source:RFAM;Acc:RF00105]"}, {"versioned_ensembl_gene_id":"ENSG00000201586.1","gene_symbol":"RNU6-593P","gene_name":"RNA, U6 small nuclear 593, pseudogene [Source:HGNC Symbol;Acc:HGNC:47556]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479828","summary":null,"start":17115652,"end":17115763,"strand":-1,"description":"RNA, U6 small nuclear 593, pseudogene [Source:HGNC Symbol;Acc:HGNC:47556]"}, {"versioned_ensembl_gene_id":"ENSG00000202474.1","gene_symbol":"RNA5SP283","gene_name":"RNA, 5S ribosomal pseudogene 283 [Source:HGNC Symbol;Acc:HGNC:43183]","synonyms":"RN5S283","biotype":"rRNA","ncbi_id":"100873536","summary":null,"start":62802320,"end":62802438,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 283 [Source:HGNC Symbol;Acc:HGNC:43183]"}, {"versioned_ensembl_gene_id":"ENSG00000264657.1","gene_symbol":"MIR3171","gene_name":"microRNA 3171 [Source:HGNC Symbol;Acc:HGNC:38216]","synonyms":"hsa-mir-3171","biotype":"miRNA","ncbi_id":"100422830","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27633205,"end":27633278,"strand":-1,"description":"microRNA 3171 [Source:HGNC Symbol;Acc:HGNC:38216]"}, {"versioned_ensembl_gene_id":"ENSG00000223087.2","gene_symbol":"RNU6-602P","gene_name":"RNA, U6 small nuclear 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:47565]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481371","summary":null,"start":31662039,"end":31662143,"strand":-1,"description":"RNA, U6 small nuclear 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:47565]"}, {"versioned_ensembl_gene_id":"ENSG00000274280.1","gene_symbol":"MIR6069","gene_name":"microRNA 6069 [Source:HGNC Symbol;Acc:HGNC:50124]","synonyms":"hsa-mir-6069","biotype":"miRNA","ncbi_id":"102464824","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35336721,"end":35336799,"strand":-1,"description":"microRNA 6069 [Source:HGNC Symbol;Acc:HGNC:50124]"}, {"versioned_ensembl_gene_id":"ENSG00000200248.1","gene_symbol":"RNA5SP214","gene_name":"RNA, 5S ribosomal pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:43114]","synonyms":"RN5S214","biotype":"rRNA","ncbi_id":"100873474","summary":null,"start":117060682,"end":117060799,"strand":1,"description":"RNA, 5S ribosomal pseudogene 214 [Source:HGNC Symbol;Acc:HGNC:43114]"}, {"versioned_ensembl_gene_id":"ENSG00000283944.1","gene_symbol":"MIR4709","gene_name":"microRNA 4709 [Source:HGNC Symbol;Acc:HGNC:41690]","synonyms":"hsa-mir-4709","biotype":"miRNA","ncbi_id":"100616211","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74480133,"end":74480204,"strand":-1,"description":"microRNA 4709 [Source:HGNC Symbol;Acc:HGNC:41690]"}, {"versioned_ensembl_gene_id":"ENSG00000199231.1","gene_symbol":"snoU2_19","gene_name":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":63175940,"end":63176019,"strand":-1,"description":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]"}, {"versioned_ensembl_gene_id":"ENSG00000284289.1","gene_symbol":"MIR6820","gene_name":"microRNA 6820 [Source:HGNC Symbol;Acc:HGNC:50095]","synonyms":"hsa-mir-6820","biotype":"miRNA","ncbi_id":"102465492","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37967563,"end":37967624,"strand":1,"description":"microRNA 6820 [Source:HGNC Symbol;Acc:HGNC:50095]"}, {"versioned_ensembl_gene_id":"ENSG00000239419.3","gene_symbol":"RN7SL535P","gene_name":"RNA, 7SL, cytoplasmic 535, pseudogene [Source:HGNC Symbol;Acc:HGNC:46551]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479417","summary":null,"start":143290615,"end":143290910,"strand":1,"description":"RNA, 7SL, cytoplasmic 535, pseudogene [Source:HGNC Symbol;Acc:HGNC:46551]"}, {"versioned_ensembl_gene_id":"ENSG00000251840.1","gene_symbol":"RN7SKP155","gene_name":"RNA, 7SK small nuclear pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:45879]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479164","summary":null,"start":123588759,"end":123589046,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 155 [Source:HGNC Symbol;Acc:HGNC:45879]"}, {"versioned_ensembl_gene_id":"ENSG00000276365.1","gene_symbol":"MIR145","gene_name":"microRNA 145 [Source:HGNC Symbol;Acc:HGNC:31532]","synonyms":"hsa-mir-145,MIRN145,MIR-145","biotype":"miRNA","ncbi_id":"406937","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":149430646,"end":149430733,"strand":1,"description":"microRNA 145 [Source:HGNC Symbol;Acc:HGNC:31532]"}, {"versioned_ensembl_gene_id":"ENSG00000222095.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100994257,"end":100994330,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000242158.3","gene_symbol":"RN7SL361P","gene_name":"RNA, 7SL, cytoplasmic 361, pseudogene [Source:HGNC Symbol;Acc:HGNC:46377]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479355","summary":null,"start":60640705,"end":60641002,"strand":1,"description":"RNA, 7SL, cytoplasmic 361, pseudogene [Source:HGNC Symbol;Acc:HGNC:46377]"}, {"versioned_ensembl_gene_id":"ENSG00000223299.1","gene_symbol":"RN7SKP108","gene_name":"RNA, 7SK small nuclear pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:45832]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480866","summary":null,"start":96638187,"end":96638514,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:45832]"}, {"versioned_ensembl_gene_id":"ENSG00000252549.1","gene_symbol":"RNU6-759P","gene_name":"RNA, U6 small nuclear 759, pseudogene [Source:HGNC Symbol;Acc:HGNC:47722]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479902","summary":null,"start":35647328,"end":35647430,"strand":-1,"description":"RNA, U6 small nuclear 759, pseudogene [Source:HGNC Symbol;Acc:HGNC:47722]"}, {"versioned_ensembl_gene_id":"ENSG00000253030.1","gene_symbol":"MIR2116","gene_name":"microRNA 2116 [Source:HGNC Symbol;Acc:HGNC:37310]","synonyms":"hsa-mir-2116","biotype":"miRNA","ncbi_id":"100313886","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59171183,"end":59171262,"strand":-1,"description":"microRNA 2116 [Source:HGNC Symbol;Acc:HGNC:37310]"}, {"versioned_ensembl_gene_id":"ENSG00000253058.1","gene_symbol":"RNA5SP437","gene_name":"RNA, 5S ribosomal pseudogene 437 [Source:HGNC Symbol;Acc:HGNC:43337]","synonyms":"RN5S437","biotype":"rRNA","ncbi_id":"100873686","summary":null,"start":31963805,"end":31963933,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 437 [Source:HGNC Symbol;Acc:HGNC:43337]"}, {"versioned_ensembl_gene_id":"ENSG00000212388.1","gene_symbol":"RNU6-796P","gene_name":"RNA, U6 small nuclear 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:47759]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481432","summary":null,"start":84939617,"end":84939723,"strand":-1,"description":"RNA, U6 small nuclear 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:47759]"}, {"versioned_ensembl_gene_id":"ENSG00000252514.1","gene_symbol":"RNU7-53P","gene_name":"RNA, U7 small nuclear 53 pseudogene [Source:HGNC Symbol;Acc:HGNC:34149]","synonyms":"U7.53","biotype":"snRNA","ncbi_id":"100151649","summary":null,"start":130386621,"end":130386680,"strand":-1,"description":"RNA, U7 small nuclear 53 pseudogene [Source:HGNC Symbol;Acc:HGNC:34149]"}, {"versioned_ensembl_gene_id":"ENSG00000263572.2","gene_symbol":"MIR7853","gene_name":"microRNA 7853 [Source:HGNC Symbol;Acc:HGNC:49933]","synonyms":"hsa-mir-7853","biotype":"miRNA","ncbi_id":"102466866","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6169304,"end":6169435,"strand":-1,"description":"microRNA 7853 [Source:HGNC Symbol;Acc:HGNC:49933]"}, {"versioned_ensembl_gene_id":"ENSG00000283798.1","gene_symbol":"MIR630","gene_name":"microRNA 630 [Source:HGNC Symbol;Acc:HGNC:32886]","synonyms":"MIRN630,hsa-mir-630","biotype":"miRNA","ncbi_id":"693215","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72587217,"end":72587313,"strand":1,"description":"microRNA 630 [Source:HGNC Symbol;Acc:HGNC:32886]"}, {"versioned_ensembl_gene_id":"ENSG00000275975.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":71368666,"end":71368968,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266019.1","gene_symbol":"MIR3609","gene_name":"microRNA 3609 [Source:HGNC Symbol;Acc:HGNC:38956]","synonyms":"hsa-mir-3609","biotype":"miRNA","ncbi_id":"100500819","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98881650,"end":98881729,"strand":1,"description":"microRNA 3609 [Source:HGNC Symbol;Acc:HGNC:38956]"}, {"versioned_ensembl_gene_id":"ENSG00000199971.1","gene_symbol":"RNU6-797P","gene_name":"RNA, U6 small nuclear 797, pseudogene [Source:HGNC Symbol;Acc:HGNC:47760]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479918","summary":null,"start":140209563,"end":140209671,"strand":-1,"description":"RNA, U6 small nuclear 797, pseudogene [Source:HGNC Symbol;Acc:HGNC:47760]"}, {"versioned_ensembl_gene_id":"ENSG00000200893.1","gene_symbol":"RNU6-944P","gene_name":"RNA, U6 small nuclear 944, pseudogene [Source:HGNC Symbol;Acc:HGNC:47907]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479983","summary":null,"start":20784509,"end":20784615,"strand":1,"description":"RNA, U6 small nuclear 944, pseudogene [Source:HGNC Symbol;Acc:HGNC:47907]"}, {"versioned_ensembl_gene_id":"ENSG00000207581.1","gene_symbol":"MIR199B","gene_name":"microRNA 199b [Source:HGNC Symbol;Acc:HGNC:31573]","synonyms":"MIRN199B,hsa-mir-199b","biotype":"miRNA","ncbi_id":"406978","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128244721,"end":128244830,"strand":-1,"description":"microRNA 199b [Source:HGNC Symbol;Acc:HGNC:31573]"}, {"versioned_ensembl_gene_id":"ENSG00000223062.1","gene_symbol":"RNU6-1245P","gene_name":"RNA, U6 small nuclear 1245, pseudogene [Source:HGNC Symbol;Acc:HGNC:48208]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480109","summary":null,"start":27824538,"end":27824643,"strand":1,"description":"RNA, U6 small nuclear 1245, pseudogene [Source:HGNC Symbol;Acc:HGNC:48208]"}, {"versioned_ensembl_gene_id":"ENSG00000221139.1","gene_symbol":"SNORD23","gene_name":"Small nucleolar RNA SNORD23 [Source:RFAM;Acc:RF00603]","synonyms":"HBII-115","biotype":"snoRNA","ncbi_id":"692091","summary":null,"start":21450653,"end":21450756,"strand":-1,"description":"Small nucleolar RNA SNORD23 [Source:RFAM;Acc:RF00603]"}, {"versioned_ensembl_gene_id":"ENSG00000212374.1","gene_symbol":"RNU6-401P","gene_name":"RNA, U6 small nuclear 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:47364]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479743","summary":null,"start":83717427,"end":83717522,"strand":1,"description":"RNA, U6 small nuclear 401, pseudogene [Source:HGNC Symbol;Acc:HGNC:47364]"}, {"versioned_ensembl_gene_id":"ENSG00000284343.1","gene_symbol":"MIR631","gene_name":"microRNA 631 [Source:HGNC Symbol;Acc:HGNC:32887]","synonyms":"MIRN631,hsa-mir-631","biotype":"miRNA","ncbi_id":"693216","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75353611,"end":75353685,"strand":-1,"description":"microRNA 631 [Source:HGNC Symbol;Acc:HGNC:32887]"}, {"versioned_ensembl_gene_id":"ENSG00000201676.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":59833175,"end":59833276,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252209.1","gene_symbol":"RNU1-48P","gene_name":"RNA, U1 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:48390]","synonyms":null,"biotype":"snRNA","ncbi_id":"107080628","summary":null,"start":18486511,"end":18486672,"strand":1,"description":"RNA, U1 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:48390]"}, {"versioned_ensembl_gene_id":"ENSG00000252909.1","gene_symbol":"RNU6-201P","gene_name":"RNA, U6 small nuclear 201, pseudogene [Source:HGNC Symbol;Acc:HGNC:47164]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481240","summary":null,"start":31837238,"end":31837298,"strand":1,"description":"RNA, U6 small nuclear 201, pseudogene [Source:HGNC Symbol;Acc:HGNC:47164]"}, {"versioned_ensembl_gene_id":"ENSG00000206887.1","gene_symbol":"RNU6-1008P","gene_name":"RNA, U6 small nuclear 1008, pseudogene [Source:HGNC Symbol;Acc:HGNC:47971]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481498","summary":null,"start":224305380,"end":224305483,"strand":1,"description":"RNA, U6 small nuclear 1008, pseudogene [Source:HGNC Symbol;Acc:HGNC:47971]"}, {"versioned_ensembl_gene_id":"ENSG00000206843.1","gene_symbol":"RNU6-206P","gene_name":"RNA, U6 small nuclear 206, pseudogene [Source:HGNC Symbol;Acc:HGNC:47169]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481882","summary":null,"start":139315291,"end":139315394,"strand":-1,"description":"RNA, U6 small nuclear 206, pseudogene [Source:HGNC Symbol;Acc:HGNC:47169]"}, {"versioned_ensembl_gene_id":"ENSG00000200600.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23994502,"end":23994603,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284385.1","gene_symbol":"MIR4313","gene_name":"microRNA 4313 [Source:HGNC Symbol;Acc:HGNC:38310]","synonyms":"hsa-mir-4313","biotype":"miRNA","ncbi_id":"100423035","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75762215,"end":75762315,"strand":-1,"description":"microRNA 4313 [Source:HGNC Symbol;Acc:HGNC:38310]"}, {"versioned_ensembl_gene_id":"ENSG00000222609.1","gene_symbol":"RNU4-69P","gene_name":"RNA, U4 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:47005]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479590","summary":null,"start":120710698,"end":120710840,"strand":-1,"description":"RNA, U4 small nuclear 69, pseudogene [Source:HGNC Symbol;Acc:HGNC:47005]"}, {"versioned_ensembl_gene_id":"ENSG00000206839.1","gene_symbol":"RNU6-746P","gene_name":"RNA, U6 small nuclear 746, pseudogene [Source:HGNC Symbol;Acc:HGNC:47709]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479896","summary":null,"start":55294490,"end":55294598,"strand":1,"description":"RNA, U6 small nuclear 746, pseudogene [Source:HGNC Symbol;Acc:HGNC:47709]"}, {"versioned_ensembl_gene_id":"ENSG00000251923.1","gene_symbol":"RNU6-276P","gene_name":"RNA, U6 small nuclear 276, pseudogene [Source:HGNC Symbol;Acc:HGNC:47239]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479689","summary":null,"start":55798636,"end":55798731,"strand":1,"description":"RNA, U6 small nuclear 276, pseudogene [Source:HGNC Symbol;Acc:HGNC:47239]"}, {"versioned_ensembl_gene_id":"ENSG00000207249.1","gene_symbol":"SNORA72","gene_name":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]","synonyms":"RNU72,U72","biotype":"snoRNA","ncbi_id":"26775","summary":null,"start":104733234,"end":104733362,"strand":1,"description":"Small nucleolar RNA SNORA72 [Source:RFAM;Acc:RF00139]"}, {"versioned_ensembl_gene_id":"ENSG00000264115.1","gene_symbol":"MIR3180-4","gene_name":"microRNA 3180-4 [Source:HGNC Symbol;Acc:HGNC:38920]","synonyms":"hsa-mir-3180-4","biotype":"miRNA","ncbi_id":"100500852","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15154850,"end":15155002,"strand":-1,"description":"microRNA 3180-4 [Source:HGNC Symbol;Acc:HGNC:38920]"}, {"versioned_ensembl_gene_id":"ENSG00000264978.2","gene_symbol":"RN7SL630P","gene_name":"RNA, 7SL, cytoplasmic 630, pseudogene [Source:HGNC Symbol;Acc:HGNC:46646]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481094","summary":null,"start":93831076,"end":93831372,"strand":1,"description":"RNA, 7SL, cytoplasmic 630, pseudogene [Source:HGNC Symbol;Acc:HGNC:46646]"}, {"versioned_ensembl_gene_id":"ENSG00000278640.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":105352670,"end":105352956,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276844.1","gene_symbol":"SNORD115-46","gene_name":"small nucleolar RNA, C/D box 115-46 [Source:HGNC Symbol;Acc:HGNC:42798]","synonyms":"HBII-52-46","biotype":"snoRNA","ncbi_id":"100873857","summary":null,"start":25266591,"end":25266661,"strand":1,"description":"small nucleolar RNA, C/D box 115-46 [Source:HGNC Symbol;Acc:HGNC:42798]"}, {"versioned_ensembl_gene_id":"ENSG00000202261.1","gene_symbol":"SNORD115-44","gene_name":"small nucleolar RNA, C/D box 115-44 [Source:HGNC Symbol;Acc:HGNC:33063]","synonyms":"HBII-52-44","biotype":"snoRNA","ncbi_id":"100033818","summary":null,"start":25250859,"end":25250940,"strand":1,"description":"small nucleolar RNA, C/D box 115-44 [Source:HGNC Symbol;Acc:HGNC:33063]"}, {"versioned_ensembl_gene_id":"ENSG00000264005.1","gene_symbol":"MIR4314","gene_name":"microRNA 4314 [Source:HGNC Symbol;Acc:HGNC:38191]","synonyms":"hsa-mir-4314","biotype":"miRNA","ncbi_id":"100422983","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8088056,"end":8088147,"strand":1,"description":"microRNA 4314 [Source:HGNC Symbol;Acc:HGNC:38191]"}, {"versioned_ensembl_gene_id":"ENSG00000284055.1","gene_symbol":"MIR4315-1","gene_name":"microRNA 4315-1 [Source:HGNC Symbol;Acc:HGNC:38342]","synonyms":"hsa-mir-4315-1","biotype":"miRNA","ncbi_id":"100423004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45475363,"end":45475435,"strand":-1,"description":"microRNA 4315-1 [Source:HGNC Symbol;Acc:HGNC:38342]"}, {"versioned_ensembl_gene_id":"ENSG00000275132.1","gene_symbol":"RN7SL663P","gene_name":"RNA, 7SL, cytoplasmic 663, pseudogene [Source:HGNC Symbol;Acc:HGNC:46679]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481103","summary":null,"start":38200234,"end":38200532,"strand":1,"description":"RNA, 7SL, cytoplasmic 663, pseudogene [Source:HGNC Symbol;Acc:HGNC:46679]"}, {"versioned_ensembl_gene_id":"ENSG00000200877.1","gene_symbol":"RNU6-560P","gene_name":"RNA, U6 small nuclear 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:47523]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480590","summary":null,"start":86153227,"end":86153334,"strand":1,"description":"RNA, U6 small nuclear 560, pseudogene [Source:HGNC Symbol;Acc:HGNC:47523]"}, {"versioned_ensembl_gene_id":"ENSG00000207972.1","gene_symbol":"MIR638","gene_name":"microRNA 638 [Source:HGNC Symbol;Acc:HGNC:32894]","synonyms":"MIRN638,hsa-mir-638","biotype":"miRNA","ncbi_id":"693223","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10718404,"end":10718503,"strand":1,"description":"microRNA 638 [Source:HGNC Symbol;Acc:HGNC:32894]"}, {"versioned_ensembl_gene_id":"ENSG00000202293.1","gene_symbol":"SNORD114-22","gene_name":"small nucleolar RNA, C/D box 114-22 [Source:HGNC Symbol;Acc:HGNC:33010]","synonyms":"14q(II-22)","biotype":"snoRNA","ncbi_id":"767600","summary":null,"start":100982926,"end":100982997,"strand":1,"description":"small nucleolar RNA, C/D box 114-22 [Source:HGNC Symbol;Acc:HGNC:33010]"}, {"versioned_ensembl_gene_id":"ENSG00000207241.1","gene_symbol":"SNORD45A","gene_name":"small nucleolar RNA, C/D box 45A [Source:HGNC Symbol;Acc:HGNC:10184]","synonyms":"U45a,RNU45A","biotype":"snoRNA","ncbi_id":"26805","summary":null,"start":75787889,"end":75787972,"strand":1,"description":"small nucleolar RNA, C/D box 45A [Source:HGNC Symbol;Acc:HGNC:10184]"}, {"versioned_ensembl_gene_id":"ENSG00000202502.1","gene_symbol":"RNA5SP151","gene_name":"RNA, 5S ribosomal pseudogene 151 [Source:HGNC Symbol;Acc:HGNC:43051]","synonyms":"RN5S151","biotype":"rRNA","ncbi_id":"100873417","summary":null,"start":183258300,"end":183258416,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 151 [Source:HGNC Symbol;Acc:HGNC:43051]"}, {"versioned_ensembl_gene_id":"ENSG00000252653.1","gene_symbol":"RNA5SP444","gene_name":"RNA, 5S ribosomal pseudogene 444 [Source:HGNC Symbol;Acc:HGNC:43344]","synonyms":"RN5S444","biotype":"rRNA","ncbi_id":"100873690","summary":null,"start":66267743,"end":66267848,"strand":1,"description":"RNA, 5S ribosomal pseudogene 444 [Source:HGNC Symbol;Acc:HGNC:43344]"}, {"versioned_ensembl_gene_id":"ENSG00000207837.1","gene_symbol":"MIR517B","gene_name":"microRNA 517b [Source:HGNC Symbol;Acc:HGNC:32115]","synonyms":"MIRN517B,hsa-mir-517b","biotype":"miRNA","ncbi_id":"574483","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53721076,"end":53721142,"strand":1,"description":"microRNA 517b [Source:HGNC Symbol;Acc:HGNC:32115]"}, {"versioned_ensembl_gene_id":"ENSG00000212248.1","gene_symbol":"RNU6-750P","gene_name":"RNA, U6 small nuclear 750, pseudogene [Source:HGNC Symbol;Acc:HGNC:47713]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479897","summary":null,"start":99978939,"end":99979045,"strand":1,"description":"RNA, U6 small nuclear 750, pseudogene [Source:HGNC Symbol;Acc:HGNC:47713]"}, {"versioned_ensembl_gene_id":"ENSG00000238316.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":26642286,"end":26642389,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000199468.1","gene_symbol":"RNU6-556P","gene_name":"RNA, U6 small nuclear 556, pseudogene [Source:HGNC Symbol;Acc:HGNC:47519]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481357","summary":null,"start":156814130,"end":156814234,"strand":1,"description":"RNA, U6 small nuclear 556, pseudogene [Source:HGNC Symbol;Acc:HGNC:47519]"}, {"versioned_ensembl_gene_id":"ENSG00000199273.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":40128121,"end":40128232,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200852.1","gene_symbol":"RNA5SP499","gene_name":"RNA, 5S ribosomal pseudogene 499 [Source:HGNC Symbol;Acc:HGNC:43399]","synonyms":"RN5S499","biotype":"rRNA","ncbi_id":"100873550","summary":null,"start":9133828,"end":9133946,"strand":1,"description":"RNA, 5S ribosomal pseudogene 499 [Source:HGNC Symbol;Acc:HGNC:43399]"}, {"versioned_ensembl_gene_id":"ENSG00000201512.1","gene_symbol":"SNORA71C","gene_name":"small nucleolar RNA, H/ACA box 71C [Source:HGNC Symbol;Acc:HGNC:32656]","synonyms":"U71c","biotype":"snoRNA","ncbi_id":"677839","summary":null,"start":38429670,"end":38429803,"strand":-1,"description":"small nucleolar RNA, H/ACA box 71C [Source:HGNC Symbol;Acc:HGNC:32656]"}, {"versioned_ensembl_gene_id":"ENSG00000211532.1","gene_symbol":"MIR526A2","gene_name":"microRNA 526a-2 [Source:HGNC Symbol;Acc:HGNC:32118]","synonyms":"hsa-mir-526a-2,MIRN526A2,MIRN526A-2","biotype":"miRNA","ncbi_id":"574486","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53726922,"end":53726986,"strand":1,"description":"microRNA 526a-2 [Source:HGNC Symbol;Acc:HGNC:32118]"}, {"versioned_ensembl_gene_id":"ENSG00000223313.1","gene_symbol":"RNU6-516P","gene_name":"RNA, U6 small nuclear 516, pseudogene [Source:HGNC Symbol;Acc:HGNC:47479]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479794","summary":null,"start":40529570,"end":40529673,"strand":1,"description":"RNA, U6 small nuclear 516, pseudogene [Source:HGNC Symbol;Acc:HGNC:47479]"}, {"versioned_ensembl_gene_id":"ENSG00000252612.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185266535,"end":185266627,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265396.1","gene_symbol":"MIR3128","gene_name":"microRNA 3128 [Source:HGNC Symbol;Acc:HGNC:38188]","synonyms":"hsa-mir-3128","biotype":"miRNA","ncbi_id":"100422824","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":177255945,"end":177256010,"strand":-1,"description":"microRNA 3128 [Source:HGNC Symbol;Acc:HGNC:38188]"}, {"versioned_ensembl_gene_id":"ENSG00000212422.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":10222797,"end":10223011,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000275072.1","gene_symbol":"SNORD50B","gene_name":"small nucleolar RNA, C/D box 50B [Source:HGNC Symbol;Acc:HGNC:32722]","synonyms":"U50B","biotype":"snoRNA","ncbi_id":"692088","summary":"SNORD50B is a C/D box-type small nucleolar RNA (snoRNA) that is predicted to function as a guide RNA in 2-prime O-methylation of 28S ribosomal RNA (Tanaka et al., 2000 [PubMed 10792466]).[supplied by OMIM, Feb 2010]","start":85677589,"end":85677658,"strand":-1,"description":"small nucleolar RNA, C/D box 50B [Source:HGNC Symbol;Acc:HGNC:32722]"}, {"versioned_ensembl_gene_id":"ENSG00000201831.1","gene_symbol":"SNORD115-1","gene_name":"small nucleolar RNA, C/D box 115-1 [Source:HGNC Symbol;Acc:HGNC:33020]","synonyms":"HBII-52-1","biotype":"snoRNA","ncbi_id":"338433","summary":"This gene encodes a small nucleolar RNA (snoRNA) that is found clustered with dozens of other similar snoRNAs on chromosome 15. These genes are found mostly within introns of the IC-SNURF-SNRPN transcript, which is paternally imprinted and from the Prader-Willi/Angelman syndrome (PWS) region. This gene has been designated as copy 1 of the cluster and may be involved in the regulation of RNA editing and/or alternative splicing of the serotonin receptor 2C (HTR2C) transcript. This gene is not thought to play a major role in PWS. [provided by RefSeq, Jul 2008]","start":25170723,"end":25170804,"strand":1,"description":"small nucleolar RNA, C/D box 115-1 [Source:HGNC Symbol;Acc:HGNC:33020]"}, {"versioned_ensembl_gene_id":"ENSG00000264623.3","gene_symbol":"MIR4796","gene_name":"microRNA 4796 [Source:HGNC Symbol;Acc:HGNC:41779]","synonyms":"hsa-mir-4796","biotype":"miRNA","ncbi_id":"100616166","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114743445,"end":114743525,"strand":-1,"description":"microRNA 4796 [Source:HGNC Symbol;Acc:HGNC:41779]"}, {"versioned_ensembl_gene_id":"ENSG00000201796.1","gene_symbol":"RNU6-392P","gene_name":"RNA, U6 small nuclear 392, pseudogene [Source:HGNC Symbol;Acc:HGNC:47355]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480577","summary":null,"start":106208167,"end":106208267,"strand":1,"description":"RNA, U6 small nuclear 392, pseudogene [Source:HGNC Symbol;Acc:HGNC:47355]"}, {"versioned_ensembl_gene_id":"ENSG00000239640.3","gene_symbol":"RN7SL62P","gene_name":"RNA, 7SL, cytoplasmic 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:46078]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479246","summary":null,"start":52714399,"end":52714695,"strand":1,"description":"RNA, 7SL, cytoplasmic 62, pseudogene [Source:HGNC Symbol;Acc:HGNC:46078]"}, {"versioned_ensembl_gene_id":"ENSG00000253041.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":101322477,"end":101322533,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000265138.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"ACA48,SNORA48A","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30123125,"end":30123286,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000251761.1","gene_symbol":"RNU6-138P","gene_name":"RNA, U6 small nuclear 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:47101]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479627","summary":null,"start":18954943,"end":18955049,"strand":-1,"description":"RNA, U6 small nuclear 138, pseudogene [Source:HGNC Symbol;Acc:HGNC:47101]"}, {"versioned_ensembl_gene_id":"ENSG00000264319.1","gene_symbol":"MIR4801","gene_name":"microRNA 4801 [Source:HGNC Symbol;Acc:HGNC:41840]","synonyms":"hsa-mir-4801","biotype":"miRNA","ncbi_id":"100616435","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37241910,"end":37241991,"strand":-1,"description":"microRNA 4801 [Source:HGNC Symbol;Acc:HGNC:41840]"}, {"versioned_ensembl_gene_id":"ENSG00000275143.1","gene_symbol":"SCARNA16","gene_name":"small Cajal body-specific RNA 16 [Source:HGNC Symbol;Acc:HGNC:32573]","synonyms":"ACA47","biotype":"scaRNA","ncbi_id":"677781","summary":null,"start":77089307,"end":77089493,"strand":1,"description":"small Cajal body-specific RNA 16 [Source:HGNC Symbol;Acc:HGNC:32573]"}, {"versioned_ensembl_gene_id":"ENSG00000275307.1","gene_symbol":"TUG1_4","gene_name":"Taurine upregulated gene 1 conserved region 4 [Source:RFAM;Acc:RF01892]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30973417,"end":30973597,"strand":1,"description":"Taurine upregulated gene 1 conserved region 4 [Source:RFAM;Acc:RF01892]"}, {"versioned_ensembl_gene_id":"ENSG00000240966.3","gene_symbol":"RN7SL681P","gene_name":"RNA, 7SL, cytoplasmic 681, pseudogene [Source:HGNC Symbol;Acc:HGNC:46697]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479471","summary":null,"start":87386883,"end":87387174,"strand":-1,"description":"RNA, 7SL, cytoplasmic 681, pseudogene [Source:HGNC Symbol;Acc:HGNC:46697]"}, {"versioned_ensembl_gene_id":"ENSG00000200593.1","gene_symbol":"SNORD115-33","gene_name":"small nucleolar RNA, C/D box 115-33 [Source:HGNC Symbol;Acc:HGNC:33052]","synonyms":"HBII-52-33","biotype":"snoRNA","ncbi_id":"100033807","summary":null,"start":25230838,"end":25230919,"strand":1,"description":"small nucleolar RNA, C/D box 115-33 [Source:HGNC Symbol;Acc:HGNC:33052]"}, {"versioned_ensembl_gene_id":"ENSG00000238478.1","gene_symbol":"RNU6-498P","gene_name":"RNA, U6 small nuclear 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:47461]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481338","summary":null,"start":20738679,"end":20738785,"strand":1,"description":"RNA, U6 small nuclear 498, pseudogene [Source:HGNC Symbol;Acc:HGNC:47461]"}, {"versioned_ensembl_gene_id":"ENSG00000275642.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1724115,"end":1724395,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222626.1","gene_symbol":"RNU2-48P","gene_name":"RNA, U2 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:48541]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481649","summary":null,"start":157976766,"end":157976956,"strand":-1,"description":"RNA, U2 small nuclear 48, pseudogene [Source:HGNC Symbol;Acc:HGNC:48541]"}, {"versioned_ensembl_gene_id":"ENSG00000240626.3","gene_symbol":"RN7SL150P","gene_name":"RNA, 7SL, cytoplasmic 150, pseudogene [Source:HGNC Symbol;Acc:HGNC:46166]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479276","summary":null,"start":33927364,"end":33927625,"strand":-1,"description":"RNA, 7SL, cytoplasmic 150, pseudogene [Source:HGNC Symbol;Acc:HGNC:46166]"}, {"versioned_ensembl_gene_id":"ENSG00000199161.1","gene_symbol":"MIR126","gene_name":"microRNA 126 [Source:HGNC Symbol;Acc:HGNC:31508]","synonyms":"hsa-mir-126,MIRN126","biotype":"miRNA","ncbi_id":"406913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136670602,"end":136670686,"strand":1,"description":"microRNA 126 [Source:HGNC Symbol;Acc:HGNC:31508]"}, {"versioned_ensembl_gene_id":"ENSG00000223162.1","gene_symbol":"RNA5SP280","gene_name":"RNA, 5S ribosomal pseudogene 280 [Source:HGNC Symbol;Acc:HGNC:43180]","synonyms":"RN5S280","biotype":"rRNA","ncbi_id":"100873533","summary":null,"start":27198287,"end":27198401,"strand":1,"description":"RNA, 5S ribosomal pseudogene 280 [Source:HGNC Symbol;Acc:HGNC:43180]"}, {"versioned_ensembl_gene_id":"ENSG00000202521.1","gene_symbol":"RNA5S7","gene_name":"RNA, 5S ribosomal 7 [Source:HGNC Symbol;Acc:HGNC:34368]","synonyms":"RN5S7","biotype":"rRNA","ncbi_id":"100169758","summary":null,"start":228623667,"end":228623785,"strand":-1,"description":"RNA, 5S ribosomal 7 [Source:HGNC Symbol;Acc:HGNC:34368]"}, {"versioned_ensembl_gene_id":"ENSG00000199448.1","gene_symbol":"RNU6-845P","gene_name":"RNA, U6 small nuclear 845, pseudogene [Source:HGNC Symbol;Acc:HGNC:47808]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479940","summary":null,"start":46556089,"end":46556191,"strand":-1,"description":"RNA, U6 small nuclear 845, pseudogene [Source:HGNC Symbol;Acc:HGNC:47808]"}, {"versioned_ensembl_gene_id":"ENSG00000222658.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":12885321,"end":12885417,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221190.1","gene_symbol":"MIR1184-2","gene_name":"microRNA 1184-2 [Source:HGNC Symbol;Acc:HGNC:38211]","synonyms":"hsa-mir-1184-2","biotype":"miRNA","ncbi_id":"100422985","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155383100,"end":155383198,"strand":-1,"description":"microRNA 1184-2 [Source:HGNC Symbol;Acc:HGNC:38211]"}, {"versioned_ensembl_gene_id":"ENSG00000252070.1","gene_symbol":"RNA5SP341","gene_name":"RNA, 5S ribosomal pseudogene 341 [Source:HGNC Symbol;Acc:HGNC:43241]","synonyms":"RN5S341","biotype":"rRNA","ncbi_id":"100873604","summary":null,"start":57450183,"end":57450299,"strand":1,"description":"RNA, 5S ribosomal pseudogene 341 [Source:HGNC Symbol;Acc:HGNC:43241]"}, {"versioned_ensembl_gene_id":"ENSG00000197334.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":9091240,"end":9091508,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199702.1","gene_symbol":"RNU6-170P","gene_name":"RNA, U6 small nuclear 170, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000223308.1","gene_symbol":"RN7SKP101","gene_name":"RNA, 7SK small nuclear pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:45825]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480864","summary":null,"start":46720193,"end":46720512,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 101 [Source:HGNC Symbol;Acc:HGNC:45825]"}, {"versioned_ensembl_gene_id":"ENSG00000201118.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":19089593,"end":19089688,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238697.1","gene_symbol":"RNU6-261P","gene_name":"RNA, U6 small nuclear 261, pseudogene [Source:HGNC Symbol;Acc:HGNC:47224]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481885","summary":null,"start":76446988,"end":76447089,"strand":-1,"description":"RNA, U6 small nuclear 261, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000206855.1","gene_symbol":"RNU6-571P","gene_name":"RNA, U6 small nuclear 571, pseudogene [Source:HGNC Symbol;Acc:HGNC:47534]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479819","summary":null,"start":68911653,"end":68911759,"strand":-1,"description":"RNA, U6 small nuclear 571, pseudogene [Source:HGNC Symbol;Acc:HGNC:47534]"}, {"versioned_ensembl_gene_id":"ENSG00000200171.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44153385,"end":44153480,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222765.1","gene_symbol":"RNU2-40P","gene_name":"RNA, U2 small nuclear 40, pseudogene [Source:HGNC Symbol;Acc:HGNC:48533]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480671","summary":null,"start":65807240,"end":65807435,"strand":-1,"description":"RNA, U2 small nuclear 40, pseudogene [Source:HGNC 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[provided by RefSeq, Apr 2009]","start":92840719,"end":92840851,"strand":1,"description":"small nucleolar RNA, H/ACA box 66 [Source:HGNC Symbol;Acc:HGNC:10223]"}, {"versioned_ensembl_gene_id":"ENSG00000206669.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36858227,"end":36858329,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223269.1","gene_symbol":"RN7SKP53","gene_name":"RNA, 7SK small nuclear pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:45777]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480849","summary":null,"start":99120176,"end":99120490,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 53 [Source:HGNC Symbol;Acc:HGNC:45777]"}, {"versioned_ensembl_gene_id":"ENSG00000200434.1","gene_symbol":"RNA5-8SP2","gene_name":"RNA, 5.8S ribosomal pseudogene 2 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000202231.1","gene_symbol":"SNORA9","gene_name":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]","synonyms":"SNORA9A,ACA9","biotype":"snoRNA","ncbi_id":"677798","summary":null,"start":100822620,"end":100822752,"strand":-1,"description":"Small nucleolar RNA SNORA9 [Source:RFAM;Acc:RF00411]"}, {"versioned_ensembl_gene_id":"ENSG00000239108.1","gene_symbol":"RNU6-1132P","gene_name":"RNA, U6 small nuclear 1132, pseudogene [Source:HGNC Symbol;Acc:HGNC:48095]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481937","summary":null,"start":132152243,"end":132152349,"strand":-1,"description":"RNA, U6 small nuclear 1132, pseudogene [Source:HGNC Symbol;Acc:HGNC:48095]"}, {"versioned_ensembl_gene_id":"ENSG00000251999.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":32791814,"end":32791946,"strand":1,"description":"Small 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{"versioned_ensembl_gene_id":"ENSG00000252590.1","gene_symbol":"RNU7-143P","gene_name":"RNA, U7 small nuclear 143 pseudogene [Source:HGNC Symbol;Acc:HGNC:45677]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479078","summary":null,"start":23450658,"end":23450722,"strand":1,"description":"RNA, U7 small nuclear 143 pseudogene [Source:HGNC Symbol;Acc:HGNC:45677]"}, {"versioned_ensembl_gene_id":"ENSG00000277168.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37953508,"end":37953780,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201846.1","gene_symbol":"RNA5SP166","gene_name":"RNA, 5S ribosomal pseudogene 166 [Source:HGNC 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[provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000239122.1","gene_symbol":"RNU2-11P","gene_name":"RNA, U2 small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:48504]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481637","summary":null,"start":195928589,"end":195928775,"strand":-1,"description":"RNA, U2 small nuclear 11, pseudogene [Source:HGNC Symbol;Acc:HGNC:48504]"}, {"versioned_ensembl_gene_id":"ENSG00000276608.1","gene_symbol":"ZNRD1-AS1_2","gene_name":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30050620,"end":30050695,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02219]"}, {"versioned_ensembl_gene_id":"ENSG00000252879.1","gene_symbol":"RN7SKP98","gene_name":"RNA, 7SK small nuclear pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:45822]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480863","summary":null,"start":212099521,"end":212099676,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 98 [Source:HGNC Symbol;Acc:HGNC:45822]"}, {"versioned_ensembl_gene_id":"ENSG00000200959.1","gene_symbol":"SNORA74A","gene_name":"small nucleolar RNA, H/ACA box 74A [Source:HGNC Symbol;Acc:HGNC:10119]","synonyms":"U19,RNU19","biotype":"snoRNA","ncbi_id":"26821","summary":null,"start":139278781,"end":139278978,"strand":1,"description":"small nucleolar RNA, H/ACA box 74A [Source:HGNC Symbol;Acc:HGNC:10119]"}, {"versioned_ensembl_gene_id":"ENSG00000200301.1","gene_symbol":"RNA5SP483","gene_name":"RNA, 5S ribosomal pseudogene 483 [Source:HGNC Symbol;Acc:HGNC:43383]","synonyms":"RN5S483","biotype":"rRNA","ncbi_id":"100873725","summary":null,"start":35195306,"end":35195423,"strand":1,"description":"RNA, 5S ribosomal pseudogene 483 [Source:HGNC Symbol;Acc:HGNC:43383]"}, {"versioned_ensembl_gene_id":"ENSG00000222285.1","gene_symbol":"RNA5SP193","gene_name":"RNA, 5S ribosomal pseudogene 193 [Source:HGNC Symbol;Acc:HGNC:43093]","synonyms":"RN5S193","biotype":"rRNA","ncbi_id":"100873455","summary":null,"start":136969200,"end":136969306,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 193 [Source:HGNC Symbol;Acc:HGNC:43093]"}, {"versioned_ensembl_gene_id":"ENSG00000277032.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93397139,"end":93397234,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252905.1","gene_symbol":"RNA5SP330","gene_name":"RNA, 5S ribosomal pseudogene 330 [Source:HGNC Symbol;Acc:HGNC:43230]","synonyms":"RN5S330","biotype":"rRNA","ncbi_id":"100873596","summary":null,"start":8845263,"end":8845358,"strand":1,"description":"RNA, 5S ribosomal pseudogene 330 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000202356.1","gene_symbol":"RNA5SP277","gene_name":"RNA, 5S ribosomal pseudogene 277 [Source:HGNC Symbol;Acc:HGNC:43177]","synonyms":"RN5S277","biotype":"rRNA","ncbi_id":"100873530","summary":null,"start":119891132,"end":119891229,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 277 [Source:HGNC Symbol;Acc:HGNC:43177]"}, {"versioned_ensembl_gene_id":"ENSG00000201700.3","gene_symbol":"SNORD113-3","gene_name":"small nucleolar RNA, C/D box 113-3 [Source:HGNC Symbol;Acc:HGNC:32982]","synonyms":"14q(I-3)","biotype":"snoRNA","ncbi_id":"767563","summary":null,"start":100929919,"end":100929990,"strand":1,"description":"small nucleolar RNA, C/D box 113-3 [Source:HGNC Symbol;Acc:HGNC:32982]"}, {"versioned_ensembl_gene_id":"ENSG00000199574.1","gene_symbol":"SNORD18C","gene_name":"small nucleolar RNA, C/D box 18C [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000277492.1","gene_symbol":"SNORD3E","gene_name":"small nucleolar RNA, C/D box 3E [Source:HGNC Symbol;Acc:HGNC:52238]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617015","summary":null,"start":70846079,"end":70846295,"strand":-1,"description":"small nucleolar RNA, C/D box 3E [Source:HGNC Symbol;Acc:HGNC:52238]"}, {"versioned_ensembl_gene_id":"ENSG00000277913.1","gene_symbol":"DLEU2_1","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 1 [Source:RFAM;Acc:RF02105]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50044649,"end":50044768,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 1 [Source:RFAM;Acc:RF02105]"}, {"versioned_ensembl_gene_id":"ENSG00000266626.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31077965,"end":31078064,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000222552.1","gene_symbol":"RNA5SP60","gene_name":"RNA, 5S ribosomal pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:42837]","synonyms":"RN5S60","biotype":"rRNA","ncbi_id":"100873295","summary":null,"start":159178473,"end":159178559,"strand":1,"description":"RNA, 5S ribosomal pseudogene 60 [Source:HGNC Symbol;Acc:HGNC:42837]"}, {"versioned_ensembl_gene_id":"ENSG00000238829.1","gene_symbol":"RNU7-45P","gene_name":"RNA, U7 small nuclear 45 pseudogene [Source:HGNC Symbol;Acc:HGNC:34141]","synonyms":"U7.45","biotype":"snRNA","ncbi_id":"100147832","summary":null,"start":201141904,"end":201141966,"strand":1,"description":"RNA, U7 small nuclear 45 pseudogene [Source:HGNC Symbol;Acc:HGNC:34141]"}, {"versioned_ensembl_gene_id":"ENSG00000206965.1","gene_symbol":"RNU6-5P","gene_name":"RNA, U6 small nuclear 5, pseudogene [Source:HGNC 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The encoded protein hydroxylates deoxyhypusine to form hypusine in the mature eukaryotic initiation factor 5A protein. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]","start":3490822,"end":3500940,"strand":-1,"description":"deoxyhypusine hydroxylase [Source:HGNC Symbol;Acc:HGNC:28662]"}, {"versioned_ensembl_gene_id":"ENSG00000252179.1","gene_symbol":"RNA5SP255","gene_name":"RNA, 5S ribosomal pseudogene 255 [Source:HGNC Symbol;Acc:HGNC:43155]","synonyms":"RN5S255","biotype":"rRNA","ncbi_id":"100873509","summary":null,"start":13536029,"end":13536135,"strand":1,"description":"RNA, 5S ribosomal pseudogene 255 [Source:HGNC Symbol;Acc:HGNC:43155]"}, {"versioned_ensembl_gene_id":"ENSG00000252560.1","gene_symbol":"RNU4-18P","gene_name":"RNA, U4 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46954]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480545","summary":null,"start":131642818,"end":131642966,"strand":-1,"description":"RNA, U4 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46954]"}, {"versioned_ensembl_gene_id":"ENSG00000199970.1","gene_symbol":"SNORD115-3","gene_name":"small nucleolar RNA, C/D box 115-3 [Source:HGNC Symbol;Acc:HGNC:33022]","synonyms":"HBII-52-3","biotype":"snoRNA","ncbi_id":"100033440","summary":null,"start":25174927,"end":25175008,"strand":1,"description":"small nucleolar RNA, C/D box 115-3 [Source:HGNC Symbol;Acc:HGNC:33022]"}, {"versioned_ensembl_gene_id":"ENSG00000212420.1","gene_symbol":"RNU6-1111P","gene_name":"RNA, U6 small nuclear 1111, pseudogene [Source:HGNC Symbol;Acc:HGNC:48074]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481530","summary":null,"start":89886485,"end":89886591,"strand":-1,"description":"RNA, U6 small nuclear 1111, pseudogene [Source:HGNC Symbol;Acc:HGNC:48074]"}, {"versioned_ensembl_gene_id":"ENSG00000207331.1","gene_symbol":"RNU6-1263P","gene_name":"RNA, U6 small nuclear 1263, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000201264.1","gene_symbol":"SNORD73B","gene_name":"small nucleolar RNA, C/D box U73B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30357]","synonyms":"U73B,RNU73B","biotype":"snoRNA","ncbi_id":"114655","summary":null,"start":151102057,"end":151102128,"strand":1,"description":"small nucleolar RNA, C/D box U73B (pseudogene) [Source:HGNC Symbol;Acc:HGNC:30357]"}, {"versioned_ensembl_gene_id":"ENSG00000276057.1","gene_symbol":"TUG1_2","gene_name":"Taurine upregulated gene 1 conserved region 2 [Source:RFAM;Acc:RF01883]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30971296,"end":30971382,"strand":1,"description":"Taurine upregulated gene 1 conserved region 2 [Source:RFAM;Acc:RF01883]"}, {"versioned_ensembl_gene_id":"ENSG00000201704.1","gene_symbol":"RNA5SP396","gene_name":"RNA, 5S ribosomal pseudogene 396 [Source:HGNC 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The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]","start":54973355,"end":54992248,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000277419.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":30405073,"end":30405179,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200615.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33004250,"end":33004345,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000202444.1","gene_symbol":"RNU5E-6P","gene_name":"RNA, U5E small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42522]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873832","summary":null,"start":44819883,"end":44819997,"strand":-1,"description":"RNA, U5E small nuclear 6, pseudogene [Source:HGNC Symbol;Acc:HGNC:42522]"}, {"versioned_ensembl_gene_id":"ENSG00000206733.1","gene_symbol":"RNU6-641P","gene_name":"RNA, U6 small nuclear 641, pseudogene [Source:HGNC Symbol;Acc:HGNC:47604]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481908","summary":null,"start":36021939,"end":36022045,"strand":-1,"description":"RNA, U6 small nuclear 641, pseudogene [Source:HGNC Symbol;Acc:HGNC:47604]"}, {"versioned_ensembl_gene_id":"ENSG00000202260.1","gene_symbol":"RN7SKP69","gene_name":"RNA, 7SK small nuclear pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:45793]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480461","summary":null,"start":17576206,"end":17576510,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 69 [Source:HGNC Symbol;Acc:HGNC:45793]"}, {"versioned_ensembl_gene_id":"ENSG00000199436.1","gene_symbol":"SNORD9","gene_name":"small nucleolar RNA, C/D box 9 [Source:HGNC Symbol;Acc:HGNC:32705]","synonyms":"mgU6-53B","biotype":"snoRNA","ncbi_id":"692053","summary":null,"start":21392150,"end":21392253,"strand":-1,"description":"small nucleolar RNA, C/D box 9 [Source:HGNC Symbol;Acc:HGNC:32705]"}, {"versioned_ensembl_gene_id":"ENSG00000206615.1","gene_symbol":"RNU6-338P","gene_name":"RNA, U6 small nuclear 338, pseudogene [Source:HGNC Symbol;Acc:HGNC:47301]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481286","summary":null,"start":31388733,"end":31388837,"strand":-1,"description":"RNA, U6 small nuclear 338, pseudogene [Source:HGNC Symbol;Acc:HGNC:47301]"}, {"versioned_ensembl_gene_id":"ENSG00000266841.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30923328,"end":30923419,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275816.1","gene_symbol":"MIR6500","gene_name":"microRNA 6500 [Source:HGNC Symbol;Acc:HGNC:49935]","synonyms":"hsa-mir-6500","biotype":"miRNA","ncbi_id":"102466656","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51060018,"end":51060103,"strand":1,"description":"microRNA 6500 [Source:HGNC Symbol;Acc:HGNC:49935]"}, {"versioned_ensembl_gene_id":"ENSG00000278406.1","gene_symbol":"PCGEM1","gene_name":"Prostate-specific transcript 1 [Source:RFAM;Acc:RF01981]","synonyms":"NCRNA00071,LINC00071,PCAT9","biotype":"misc_RNA","ncbi_id":"64002","summary":"This gene produces a long non-coding RNA that is overexpressed in prostate cancer and may act a marker for tumor progression. This RNA may act a negative regulator of apoptosis, and may promote activity of androgen receptor and Myc. [provided by RefSeq, Dec 2017]","start":192775943,"end":192776073,"strand":1,"description":"Prostate-specific transcript 1 [Source:RFAM;Acc:RF01981]"}, {"versioned_ensembl_gene_id":"ENSG00000284482.1","gene_symbol":"MIR4680","gene_name":"microRNA 4680 [Source:HGNC Symbol;Acc:HGNC:41541]","synonyms":"hsa-mir-4680","biotype":"miRNA","ncbi_id":"100616113","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110898090,"end":110898155,"strand":1,"description":"microRNA 4680 [Source:HGNC Symbol;Acc:HGNC:41541]"}, {"versioned_ensembl_gene_id":"ENSG00000207279.1","gene_symbol":"SNORD116-24","gene_name":"small nucleolar RNA, C/D box 116-24 [Source:HGNC Symbol;Acc:HGNC:33090]","synonyms":"HBII-85-24","biotype":"snoRNA","ncbi_id":"100033435","summary":null,"start":25094037,"end":25094128,"strand":1,"description":"small nucleolar RNA, C/D box 116-24 [Source:HGNC Symbol;Acc:HGNC:33090]"}, {"versioned_ensembl_gene_id":"ENSG00000275909.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48432927,"end":48433208,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000275577.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000273830.1","gene_symbol":"MIR7843","gene_name":"microRNA 7843 [Source:HGNC Symbol;Acc:HGNC:50074]","synonyms":"hsa-mir-7843","biotype":"miRNA","ncbi_id":"102465832","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72516820,"end":72516898,"strand":1,"description":"microRNA 7843 [Source:HGNC Symbol;Acc:HGNC:50074]"}, {"versioned_ensembl_gene_id":"ENSG00000283588.1","gene_symbol":"MIR376A1","gene_name":"microRNA 376a-1 [Source:HGNC Symbol;Acc:HGNC:31869]","synonyms":"MIRN376A1,MIRN376A,hsa-mir-376a-1,hsa-mir-376a","biotype":"miRNA","ncbi_id":"494325","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101040782,"end":101040849,"strand":1,"description":"microRNA 376a-1 [Source:HGNC Symbol;Acc:HGNC:31869]"}, {"versioned_ensembl_gene_id":"ENSG00000201894.1","gene_symbol":"RNU6-967P","gene_name":"RNA, U6 small nuclear 967, pseudogene [Source:HGNC Symbol;Acc:HGNC:47930]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479993","summary":null,"start":31787148,"end":31787255,"strand":-1,"description":"RNA, U6 small nuclear 967, pseudogene [Source:HGNC Symbol;Acc:HGNC:47930]"}, {"versioned_ensembl_gene_id":"ENSG00000199627.1","gene_symbol":"RNU6-1010P","gene_name":"RNA, U6 small nuclear 1010, pseudogene [Source:HGNC Symbol;Acc:HGNC:47973]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481929","summary":null,"start":131054886,"end":131054992,"strand":-1,"description":"RNA, U6 small nuclear 1010, pseudogene [Source:HGNC Symbol;Acc:HGNC:47973]"}, {"versioned_ensembl_gene_id":"ENSG00000243420.3","gene_symbol":"RN7SL734P","gene_name":"RNA, 7SL, cytoplasmic 734, pseudogene [Source:HGNC Symbol;Acc:HGNC:46750]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479490","summary":null,"start":75957833,"end":75958130,"strand":-1,"description":"RNA, 7SL, cytoplasmic 734, pseudogene [Source:HGNC Symbol;Acc:HGNC:46750]"}, {"versioned_ensembl_gene_id":"ENSG00000200687.1","gene_symbol":"RNA5SP335","gene_name":"RNA, 5S ribosomal pseudogene 335 [Source:HGNC Symbol;Acc:HGNC:43235]","synonyms":"RN5S335","biotype":"rRNA","ncbi_id":"106479007","summary":null,"start":19401872,"end":19401981,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 335 [Source:HGNC Symbol;Acc:HGNC:43235]"}, {"versioned_ensembl_gene_id":"ENSG00000199092.4","gene_symbol":"MIR410","gene_name":"microRNA 410 [Source:HGNC Symbol;Acc:HGNC:32065]","synonyms":"MIRN410,hsa-mir-410","biotype":"miRNA","ncbi_id":"574434","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101065912,"end":101065991,"strand":1,"description":"microRNA 410 [Source:HGNC Symbol;Acc:HGNC:32065]"}, {"versioned_ensembl_gene_id":"ENSG00000202345.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":168791498,"end":168791610,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283736.1","gene_symbol":"MIR484","gene_name":"microRNA 484 [Source:HGNC Symbol;Acc:HGNC:32341]","synonyms":"MIRN484,hsa-mir-484","biotype":"miRNA","ncbi_id":"619553","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15643294,"end":15643372,"strand":1,"description":"microRNA 484 [Source:HGNC Symbol;Acc:HGNC:32341]"}, {"versioned_ensembl_gene_id":"ENSG00000274866.1","gene_symbol":"H19_2","gene_name":"H19 conserved region 2 [Source:RFAM;Acc:RF01973]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1997484,"end":1997552,"strand":1,"description":"H19 conserved region 2 [Source:RFAM;Acc:RF01973]"}, {"versioned_ensembl_gene_id":"ENSG00000278221.1","gene_symbol":"MIR6511A2","gene_name":"microRNA 6511a-2 [Source:HGNC Symbol;Acc:HGNC:50150]","synonyms":"hsa-mir-6511a-2","biotype":"miRNA","ncbi_id":"102466812","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16324588,"end":16324654,"strand":1,"description":"microRNA 6511a-2 [Source:HGNC Symbol;Acc:HGNC:50150]"}, {"versioned_ensembl_gene_id":"ENSG00000284424.1","gene_symbol":"MIR4724","gene_name":"microRNA 4724 [Source:HGNC Symbol;Acc:HGNC:41590]","synonyms":"hsa-mir-4724","biotype":"miRNA","ncbi_id":"100616248","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31534883,"end":31534971,"strand":1,"description":"microRNA 4724 [Source:HGNC Symbol;Acc:HGNC:41590]"}, {"versioned_ensembl_gene_id":"ENSG00000239010.1","gene_symbol":"RNU7-74P","gene_name":"RNA, U7 small nuclear 74 pseudogene [Source:HGNC Symbol;Acc:HGNC:34170]","synonyms":"U7.74","biotype":"snRNA","ncbi_id":"100151671","summary":null,"start":40377452,"end":40377513,"strand":-1,"description":"RNA, U7 small nuclear 74 pseudogene [Source:HGNC Symbol;Acc:HGNC:34170]"}, {"versioned_ensembl_gene_id":"ENSG00000199975.1","gene_symbol":"RN7SKP243","gene_name":"RNA, 7SK small nuclear pseudogene 243 [Source:HGNC Symbol;Acc:HGNC:45967]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481819","summary":null,"start":73832382,"end":73832690,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 243 [Source:HGNC Symbol;Acc:HGNC:45967]"}, {"versioned_ensembl_gene_id":"ENSG00000277057.1","gene_symbol":"MIR6779","gene_name":"microRNA 6779 [Source:HGNC Symbol;Acc:HGNC:50148]","synonyms":"hsa-mir-6779","biotype":"miRNA","ncbi_id":"102465467","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38914979,"end":38915042,"strand":1,"description":"microRNA 6779 [Source:HGNC Symbol;Acc:HGNC:50148]"}, {"versioned_ensembl_gene_id":"ENSG00000199196.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":34100711,"end":34100838,"strand":-1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000274566.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55021410,"end":55045969,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000221102.1","gene_symbol":"SNORA11B","gene_name":"small nucleolar RNA, H/ACA box 11B [Source:HGNC Symbol;Acc:HGNC:33620]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100124539","summary":null,"start":91126425,"end":91126553,"strand":1,"description":"small nucleolar RNA, H/ACA box 11B [Source:HGNC Symbol;Acc:HGNC:33620]"}, {"versioned_ensembl_gene_id":"ENSG00000207735.1","gene_symbol":"MIR520D","gene_name":"microRNA 520d [Source:HGNC Symbol;Acc:HGNC:32114]","synonyms":"MIRN520D,hsa-mir-520d","biotype":"miRNA","ncbi_id":"574482","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53720096,"end":53720182,"strand":1,"description":"microRNA 520d [Source:HGNC Symbol;Acc:HGNC:32114]"}, {"versioned_ensembl_gene_id":"ENSG00000207647.1","gene_symbol":"MIR153-1","gene_name":"microRNA 153-1 [Source:HGNC Symbol;Acc:HGNC:31539]","synonyms":"MIRN153-1,hsa-mir-153-1","biotype":"miRNA","ncbi_id":"406944","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219294111,"end":219294200,"strand":-1,"description":"microRNA 153-1 [Source:HGNC Symbol;Acc:HGNC:31539]"}, {"versioned_ensembl_gene_id":"ENSG00000240098.3","gene_symbol":"RN7SL351P","gene_name":"RNA, 7SL, cytoplasmic 351, pseudogene [Source:HGNC Symbol;Acc:HGNC:46367]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479351","summary":null,"start":126245035,"end":126245282,"strand":1,"description":"RNA, 7SL, cytoplasmic 351, pseudogene [Source:HGNC Symbol;Acc:HGNC:46367]"}, {"versioned_ensembl_gene_id":"ENSG00000284508.1","gene_symbol":"MIR133A2","gene_name":"microRNA 133a-2 [Source:HGNC Symbol;Acc:HGNC:31518]","synonyms":"MIRN133A2,hsa-mir-133a-2","biotype":"miRNA","ncbi_id":"406923","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62564912,"end":62565013,"strand":1,"description":"microRNA 133a-2 [Source:HGNC Symbol;Acc:HGNC:31518]"}, {"versioned_ensembl_gene_id":"ENSG00000278232.4","gene_symbol":"CRHR1","gene_name":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]","synonyms":"CRF1,CRF-R,CRHR,CRF1,CRF-R,CRHR","biotype":"protein_coding","ncbi_id":"1394","summary":"This gene encodes a G-protein coupled receptor that binds neuropeptides of the corticotropin releasing hormone family that are major regulators of the hypothalamic-pituitary-adrenal pathway. The encoded protein is essential for the activation of signal transduction pathways that regulate diverse physiological processes including stress, reproduction, immune response and obesity. Alternative splicing results in multiple transcript variants. Naturally-occurring readthrough transcription between this gene and upstream GeneID:147081 results in transcripts that encode isoforms that share similarity with the products of this gene. [provided by RefSeq, Aug 2016]","start":46261820,"end":46313387,"strand":-1,"description":"corticotropin releasing hormone receptor 1 [Source:HGNC Symbol;Acc:HGNC:2357]"}, {"versioned_ensembl_gene_id":"ENSG00000207962.1","gene_symbol":"MIR30C1","gene_name":"microRNA 30c-1 [Source:HGNC Symbol;Acc:HGNC:31626]","synonyms":"MIRN30C1,hsa-mir-30c-1","biotype":"miRNA","ncbi_id":"407031","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40757284,"end":40757372,"strand":1,"description":"microRNA 30c-1 [Source:HGNC Symbol;Acc:HGNC:31626]"}, {"versioned_ensembl_gene_id":"ENSG00000265956.1","gene_symbol":"MIR4445","gene_name":"microRNA 4445 [Source:HGNC Symbol;Acc:HGNC:41614]","synonyms":"hsa-mir-4445","biotype":"miRNA","ncbi_id":"100616129","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109602828,"end":109602897,"strand":1,"description":"microRNA 4445 [Source:HGNC Symbol;Acc:HGNC:41614]"}, {"versioned_ensembl_gene_id":"ENSG00000274603.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99526097,"end":99526205,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201326.1","gene_symbol":"SNORD115-22","gene_name":"small nucleolar RNA, C/D box 115-22 [Source:HGNC Symbol;Acc:HGNC:33041]","synonyms":"HBII-52-22","biotype":"snoRNA","ncbi_id":"100033799","summary":null,"start":25209918,"end":25209999,"strand":1,"description":"small nucleolar RNA, C/D box 115-22 [Source:HGNC Symbol;Acc:HGNC:33041]"}, {"versioned_ensembl_gene_id":"ENSG00000251822.1","gene_symbol":"SNORA19","gene_name":"Small nucleolar RNA SNORA19 [Source:RFAM;Acc:RF00413]","synonyms":"ACA19","biotype":"snoRNA","ncbi_id":"641451","summary":null,"start":60363822,"end":60363935,"strand":1,"description":"Small nucleolar RNA SNORA19 [Source:RFAM;Acc:RF00413]"}, {"versioned_ensembl_gene_id":"ENSG00000202503.1","gene_symbol":"SNORD34","gene_name":"small nucleolar RNA, C/D box 34 [Source:HGNC Symbol;Acc:HGNC:10161]","synonyms":"U34,RNU34","biotype":"snoRNA","ncbi_id":"26817","summary":null,"start":49490904,"end":49490974,"strand":1,"description":"small nucleolar RNA, C/D box 34 [Source:HGNC Symbol;Acc:HGNC:10161]"}, {"versioned_ensembl_gene_id":"ENSG00000215938.3","gene_symbol":"MIR190B","gene_name":"microRNA 190b [Source:HGNC Symbol;Acc:HGNC:33656]","synonyms":"MIRN190B,hsa-mir-190b","biotype":"miRNA","ncbi_id":"100126346","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154193665,"end":154193743,"strand":-1,"description":"microRNA 190b [Source:HGNC Symbol;Acc:HGNC:33656]"}, {"versioned_ensembl_gene_id":"ENSG00000281295.1","gene_symbol":"SNORA50B","gene_name":"small nucleolar RNA, H/ACA box 50B [Source:HGNC Symbol;Acc:HGNC:50432]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616998","summary":null,"start":33704786,"end":33704922,"strand":-1,"description":"small nucleolar RNA, H/ACA box 50B [Source:HGNC Symbol;Acc:HGNC:50432]"}, {"versioned_ensembl_gene_id":"ENSG00000266494.1","gene_symbol":"MIR4641","gene_name":"microRNA 4641 [Source:HGNC Symbol;Acc:HGNC:41835]","synonyms":"hsa-mir-4641","biotype":"miRNA","ncbi_id":"100616178","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41598723,"end":41598788,"strand":1,"description":"microRNA 4641 [Source:HGNC Symbol;Acc:HGNC:41835]"}, {"versioned_ensembl_gene_id":"ENSG00000207974.1","gene_symbol":"MIR557","gene_name":"microRNA 557 [Source:HGNC Symbol;Acc:HGNC:32813]","synonyms":"MIRN557,hsa-mir-557","biotype":"miRNA","ncbi_id":"693142","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168375524,"end":168375621,"strand":1,"description":"microRNA 557 [Source:HGNC Symbol;Acc:HGNC:32813]"}, {"versioned_ensembl_gene_id":"ENSG00000266617.1","gene_symbol":"MIR3692","gene_name":"microRNA 3692 [Source:HGNC Symbol;Acc:HGNC:38885]","synonyms":"hsa-mir-3692","biotype":"miRNA","ncbi_id":"100500899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":157529132,"end":157529200,"strand":1,"description":"microRNA 3692 [Source:HGNC Symbol;Acc:HGNC:38885]"}, {"versioned_ensembl_gene_id":"ENSG00000284203.1","gene_symbol":"MIR29B2","gene_name":"microRNA 29b-2 [Source:HGNC Symbol;Acc:HGNC:31620]","synonyms":"MIRN29B2,hsa-mir-29b-2","biotype":"miRNA","ncbi_id":"407025","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207802443,"end":207802523,"strand":-1,"description":"microRNA 29b-2 [Source:HGNC Symbol;Acc:HGNC:31620]"}, {"versioned_ensembl_gene_id":"ENSG00000242853.3","gene_symbol":"RN7SL749P","gene_name":"RNA, 7SL, cytoplasmic 749, pseudogene [Source:HGNC Symbol;Acc:HGNC:46765]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479494","summary":null,"start":119212857,"end":119213146,"strand":1,"description":"RNA, 7SL, cytoplasmic 749, pseudogene [Source:HGNC Symbol;Acc:HGNC:46765]"}, {"versioned_ensembl_gene_id":"ENSG00000208025.1","gene_symbol":"MIR591","gene_name":"microRNA 591 [Source:HGNC Symbol;Acc:HGNC:32847]","synonyms":"MIRN591,hsa-mir-591","biotype":"miRNA","ncbi_id":"693176","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96219662,"end":96219756,"strand":-1,"description":"microRNA 591 [Source:HGNC Symbol;Acc:HGNC:32847]"}, {"versioned_ensembl_gene_id":"ENSG00000240993.3","gene_symbol":"RN7SL459P","gene_name":"RNA, 7SL, cytoplasmic 459, pseudogene [Source:HGNC Symbol;Acc:HGNC:46475]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479390","summary":null,"start":19176288,"end":19176589,"strand":-1,"description":"RNA, 7SL, cytoplasmic 459, pseudogene [Source:HGNC Symbol;Acc:HGNC:46475]"}, {"versioned_ensembl_gene_id":"ENSG00000223254.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":85264296,"end":85264402,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265442.1","gene_symbol":"MIR3941","gene_name":"microRNA 3941 [Source:HGNC Symbol;Acc:HGNC:38949]","synonyms":"hsa-mir-3941","biotype":"miRNA","ncbi_id":"100500866","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122416965,"end":122417067,"strand":1,"description":"microRNA 3941 [Source:HGNC Symbol;Acc:HGNC:38949]"}, {"versioned_ensembl_gene_id":"ENSG00000284191.1","gene_symbol":"MIR671","gene_name":"microRNA 671 [Source:HGNC Symbol;Acc:HGNC:33134]","synonyms":"MIRN671,hsa-mir-671","biotype":"miRNA","ncbi_id":"768213","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151238421,"end":151238538,"strand":1,"description":"microRNA 671 [Source:HGNC Symbol;Acc:HGNC:33134]"}, {"versioned_ensembl_gene_id":"ENSG00000283165.1","gene_symbol":"MIR203B","gene_name":"microRNA 203b [Source:HGNC Symbol;Acc:HGNC:41811]","synonyms":"MIR3545,hsa-mir-3545","biotype":"miRNA","ncbi_id":"100616173","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":104117418,"end":104117503,"strand":-1,"description":"microRNA 203b [Source:HGNC Symbol;Acc:HGNC:41811]"}, {"versioned_ensembl_gene_id":"ENSG00000199837.1","gene_symbol":"RNA5SP71","gene_name":"RNA, 5S ribosomal pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:42848]","synonyms":"RN5S71","biotype":"rRNA","ncbi_id":"100873305","summary":null,"start":182944365,"end":182944490,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 71 [Source:HGNC Symbol;Acc:HGNC:42848]"}, {"versioned_ensembl_gene_id":"ENSG00000221261.1","gene_symbol":"MIR1208","gene_name":"microRNA 1208 [Source:HGNC Symbol;Acc:HGNC:35274]","synonyms":"MIRN1208,hsa-mir-1208","biotype":"miRNA","ncbi_id":"100302281","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128150116,"end":128150188,"strand":1,"description":"microRNA 1208 [Source:HGNC Symbol;Acc:HGNC:35274]"}, {"versioned_ensembl_gene_id":"ENSG00000265102.1","gene_symbol":"MIR3942","gene_name":"microRNA 3942 [Source:HGNC Symbol;Acc:HGNC:38976]","synonyms":"hsa-mir-3942","biotype":"miRNA","ncbi_id":"100500904","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35372256,"end":35372364,"strand":-1,"description":"microRNA 3942 [Source:HGNC Symbol;Acc:HGNC:38976]"}, {"versioned_ensembl_gene_id":"ENSG00000283351.1","gene_symbol":"MIR3910-2","gene_name":"microRNA 3910-2 [Source:HGNC Symbol;Acc:HGNC:38952]","synonyms":"hsa-mir-3910-2","biotype":"miRNA","ncbi_id":"100500902","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91636264,"end":91636345,"strand":-1,"description":"microRNA 3910-2 [Source:HGNC Symbol;Acc:HGNC:38952]"}, {"versioned_ensembl_gene_id":"ENSG00000207326.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":246426006,"end":246426119,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207349.1","gene_symbol":"RNVU1-17","gene_name":"RNA, variant U1 small nuclear 17 [Source:HGNC Symbol;Acc:HGNC:48322]","synonyms":"vU1.17,RNU1-127","biotype":"snRNA","ncbi_id":"101954269","summary":null,"start":143699456,"end":143699619,"strand":-1,"description":"RNA, variant U1 small nuclear 17 [Source:HGNC Symbol;Acc:HGNC:48322]"}, {"versioned_ensembl_gene_id":"ENSG00000202188.1","gene_symbol":"SNORD115-31","gene_name":"small nucleolar RNA, C/D box 115-31 [Source:HGNC Symbol;Acc:HGNC:33050]","synonyms":"HBII-52-31","biotype":"snoRNA","ncbi_id":"100033805","summary":null,"start":25227109,"end":25227190,"strand":1,"description":"small nucleolar RNA, C/D box 115-31 [Source:HGNC Symbol;Acc:HGNC:33050]"}, {"versioned_ensembl_gene_id":"ENSG00000284250.1","gene_symbol":"MIR6516","gene_name":"microRNA 6516 [Source:HGNC Symbol;Acc:HGNC:50233]","synonyms":"hsa-mir-6516","biotype":"miRNA","ncbi_id":"102466864","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77089417,"end":77089497,"strand":1,"description":"microRNA 6516 [Source:HGNC Symbol;Acc:HGNC:50233]"}, {"versioned_ensembl_gene_id":"ENSG00000207270.1","gene_symbol":"RNU6-601P","gene_name":"RNA, U6 small nuclear 601, pseudogene [Source:HGNC Symbol;Acc:HGNC:47564]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479832","summary":null,"start":149610668,"end":149610774,"strand":-1,"description":"RNA, U6 small nuclear 601, pseudogene [Source:HGNC Symbol;Acc:HGNC:47564]"}, {"versioned_ensembl_gene_id":"ENSG00000200926.1","gene_symbol":"RNU6-960P","gene_name":"RNA, U6 small nuclear 960, pseudogene [Source:HGNC Symbol;Acc:HGNC:47923]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479991","summary":null,"start":111091213,"end":111091332,"strand":-1,"description":"RNA, U6 small nuclear 960, pseudogene [Source:HGNC Symbol;Acc:HGNC:47923]"}, {"versioned_ensembl_gene_id":"ENSG00000283514.1","gene_symbol":"MIR3975","gene_name":"microRNA 3975 [Source:HGNC Symbol;Acc:HGNC:41613]","synonyms":"hsa-mir-3975","biotype":"miRNA","ncbi_id":"100616257","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35591737,"end":35591806,"strand":1,"description":"microRNA 3975 [Source:HGNC Symbol;Acc:HGNC:41613]"}, {"versioned_ensembl_gene_id":"ENSG00000240853.3","gene_symbol":"RN7SL328P","gene_name":"RNA, 7SL, cytoplasmic 328, pseudogene [Source:HGNC Symbol;Acc:HGNC:46344]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481837","summary":null,"start":131725168,"end":131725467,"strand":-1,"description":"RNA, 7SL, cytoplasmic 328, pseudogene [Source:HGNC Symbol;Acc:HGNC:46344]"}, {"versioned_ensembl_gene_id":"ENSG00000265954.1","gene_symbol":"MIR4749","gene_name":"microRNA 4749 [Source:HGNC Symbol;Acc:HGNC:41760]","synonyms":"hsa-mir-4749","biotype":"miRNA","ncbi_id":"100616313","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49854591,"end":49854651,"strand":1,"description":"microRNA 4749 [Source:HGNC Symbol;Acc:HGNC:41760]"}, {"versioned_ensembl_gene_id":"ENSG00000202337.1","gene_symbol":"RNU6-8","gene_name":"RNA, U6 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:34285]","synonyms":"U6-8","biotype":"snRNA","ncbi_id":"101954278","summary":null,"start":32203163,"end":32203269,"strand":-1,"description":"RNA, U6 small nuclear 8 [Source:HGNC Symbol;Acc:HGNC:34285]"}, {"versioned_ensembl_gene_id":"ENSG00000223189.1","gene_symbol":"RNU6-177P","gene_name":"RNA, U6 small nuclear 177, pseudogene [Source:HGNC Symbol;Acc:HGNC:47140]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481232","summary":null,"start":128627172,"end":128627275,"strand":1,"description":"RNA, U6 small nuclear 177, pseudogene [Source:HGNC Symbol;Acc:HGNC:47140]"}, {"versioned_ensembl_gene_id":"ENSG00000207981.1","gene_symbol":"MIR519D","gene_name":"microRNA 519d [Source:HGNC Symbol;Acc:HGNC:32112]","synonyms":"MIRN519D,hsa-mir-519d","biotype":"miRNA","ncbi_id":"574480","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53713347,"end":53713434,"strand":1,"description":"microRNA 519d [Source:HGNC Symbol;Acc:HGNC:32112]"}, {"versioned_ensembl_gene_id":"ENSG00000207461.1","gene_symbol":"RNU6-253P","gene_name":"RNA, U6 small nuclear 253, pseudogene [Source:HGNC Symbol;Acc:HGNC:47216]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480697","summary":null,"start":117457734,"end":117457838,"strand":-1,"description":"RNA, U6 small nuclear 253, pseudogene [Source:HGNC Symbol;Acc:HGNC:47216]"}, {"versioned_ensembl_gene_id":"ENSG00000215973.1","gene_symbol":"MIR933","gene_name":"microRNA 933 [Source:HGNC Symbol;Acc:HGNC:33676]","synonyms":"MIRN933,hsa-mir-933","biotype":"miRNA","ncbi_id":"100126350","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":175167633,"end":175167709,"strand":-1,"description":"microRNA 933 [Source:HGNC Symbol;Acc:HGNC:33676]"}, {"versioned_ensembl_gene_id":"ENSG00000201229.1","gene_symbol":"SNORA63D","gene_name":"small nucleolar RNA, H/ACA box 63D [Source:HGNC Symbol;Acc:HGNC:52211]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616971","summary":null,"start":183451857,"end":183451988,"strand":1,"description":"small nucleolar RNA, H/ACA box 63D [Source:HGNC Symbol;Acc:HGNC:52211]"}, {"versioned_ensembl_gene_id":"ENSG00000243871.3","gene_symbol":"RN7SL487P","gene_name":"RNA, 7SL, cytoplasmic 487, pseudogene [Source:HGNC Symbol;Acc:HGNC:46503]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481055","summary":null,"start":43391384,"end":43391727,"strand":-1,"description":"RNA, 7SL, cytoplasmic 487, pseudogene [Source:HGNC Symbol;Acc:HGNC:46503]"}, {"versioned_ensembl_gene_id":"ENSG00000214305.4","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39161270,"end":39161520,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207744.1","gene_symbol":"MIR10B","gene_name":"microRNA 10b [Source:HGNC Symbol;Acc:HGNC:31498]","synonyms":"hsa-mir-10b,MIRN10B","biotype":"miRNA","ncbi_id":"406903","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176150303,"end":176150412,"strand":1,"description":"microRNA 10b [Source:HGNC Symbol;Acc:HGNC:31498]"}, {"versioned_ensembl_gene_id":"ENSG00000265159.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33353481,"end":33353576,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199032.1","gene_symbol":"MIR425","gene_name":"microRNA 425 [Source:HGNC Symbol;Acc:HGNC:31882]","synonyms":"MIRN425,hsa-mir-425","biotype":"miRNA","ncbi_id":"494337","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49020148,"end":49020234,"strand":-1,"description":"microRNA 425 [Source:HGNC Symbol;Acc:HGNC:31882]"}, {"versioned_ensembl_gene_id":"ENSG00000201279.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3663815,"end":3663911,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212560.1","gene_symbol":"RNU6-630P","gene_name":"RNA, U6 small nuclear 630, pseudogene [Source:HGNC Symbol;Acc:HGNC:47593]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481380","summary":null,"start":42139425,"end":42139530,"strand":-1,"description":"RNA, U6 small nuclear 630, pseudogene [Source:HGNC Symbol;Acc:HGNC:47593]"}, {"versioned_ensembl_gene_id":"ENSG00000275334.1","gene_symbol":"MIR5787","gene_name":"microRNA 5787 [Source:HGNC Symbol;Acc:HGNC:49930]","synonyms":"hsa-mir-5787","biotype":"miRNA","ncbi_id":"102464817","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50227436,"end":50227490,"strand":1,"description":"microRNA 5787 [Source:HGNC Symbol;Acc:HGNC:49930]"}, {"versioned_ensembl_gene_id":"ENSG00000238441.1","gene_symbol":"RNU7-130P","gene_name":"RNA, U7 small nuclear 130 pseudogene [Source:HGNC Symbol;Acc:HGNC:45664]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479074","summary":null,"start":35632963,"end":35633024,"strand":-1,"description":"RNA, U7 small nuclear 130 pseudogene [Source:HGNC Symbol;Acc:HGNC:45664]"}, {"versioned_ensembl_gene_id":"ENSG00000207988.1","gene_symbol":"MIR576","gene_name":"microRNA 576 [Source:HGNC Symbol;Acc:HGNC:32832]","synonyms":"hsa-mir-576,MIRN576","biotype":"miRNA","ncbi_id":"693161","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109488698,"end":109488795,"strand":1,"description":"microRNA 576 [Source:HGNC Symbol;Acc:HGNC:32832]"}, {"versioned_ensembl_gene_id":"ENSG00000212296.1","gene_symbol":"SNORD72","gene_name":"small nucleolar RNA, C/D box 72 [Source:HGNC Symbol;Acc:HGNC:32733]","synonyms":"HBII-240","biotype":"snoRNA","ncbi_id":"619564","summary":null,"start":40832656,"end":40832735,"strand":-1,"description":"small nucleolar RNA, C/D box 72 [Source:HGNC Symbol;Acc:HGNC:32733]"}, {"versioned_ensembl_gene_id":"ENSG00000206712.1","gene_symbol":"RNU6-26P","gene_name":"RNA, U6 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:34252]","synonyms":"RNU6-26","biotype":"snRNA","ncbi_id":"100873741","summary":null,"start":98804978,"end":98805084,"strand":-1,"description":"RNA, U6 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:34252]"}, {"versioned_ensembl_gene_id":"ENSG00000283550.1","gene_symbol":"MIR2054","gene_name":"microRNA 2054 [Source:HGNC Symbol;Acc:HGNC:37070]","synonyms":"hsa-mir-2054","biotype":"miRNA","ncbi_id":"100302267","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125507259,"end":125507307,"strand":1,"description":"microRNA 2054 [Source:HGNC Symbol;Acc:HGNC:37070]"}, {"versioned_ensembl_gene_id":"ENSG00000199885.1","gene_symbol":"RNU6-330P","gene_name":"RNA, U6 small nuclear 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:47293]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481283","summary":null,"start":74680053,"end":74680159,"strand":1,"description":"RNA, U6 small nuclear 330, pseudogene [Source:HGNC Symbol;Acc:HGNC:47293]"}, {"versioned_ensembl_gene_id":"ENSG00000273549.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":179629151,"end":179629410,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201909.1","gene_symbol":"RNU6-590P","gene_name":"RNA, U6 small nuclear 590, pseudogene [Source:HGNC Symbol;Acc:HGNC:47553]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480593","summary":null,"start":13459670,"end":13459776,"strand":-1,"description":"RNA, U6 small nuclear 590, pseudogene [Source:HGNC Symbol;Acc:HGNC:47553]"}, {"versioned_ensembl_gene_id":"ENSG00000252891.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":89898283,"end":89898392,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264563.1","gene_symbol":"MIR4633","gene_name":"microRNA 4633 [Source:HGNC Symbol;Acc:HGNC:41822]","synonyms":"hsa-mir-4633","biotype":"miRNA","ncbi_id":"100616175","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129097688,"end":129097766,"strand":1,"description":"microRNA 4633 [Source:HGNC Symbol;Acc:HGNC:41822]"}, {"versioned_ensembl_gene_id":"ENSG00000199846.1","gene_symbol":"RNU1-72P","gene_name":"RNA, U1 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:48414]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481955","summary":null,"start":129484504,"end":129484656,"strand":1,"description":"RNA, U1 small nuclear 72, pseudogene [Source:HGNC Symbol;Acc:HGNC:48414]"}, {"versioned_ensembl_gene_id":"ENSG00000212535.1","gene_symbol":"RNU6-808P","gene_name":"RNA, U6 small nuclear 808, pseudogene [Source:HGNC Symbol;Acc:HGNC:47771]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481436","summary":null,"start":95290692,"end":95290799,"strand":1,"description":"RNA, U6 small nuclear 808, pseudogene [Source:HGNC Symbol;Acc:HGNC:47771]"}, {"versioned_ensembl_gene_id":"ENSG00000221552.1","gene_symbol":"MIR1303","gene_name":"microRNA 1303 [Source:HGNC Symbol;Acc:HGNC:35301]","synonyms":"MIRN1303,hsa-mir-1303","biotype":"miRNA","ncbi_id":"100302284","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154685776,"end":154685861,"strand":1,"description":"microRNA 1303 [Source:HGNC Symbol;Acc:HGNC:35301]"}, {"versioned_ensembl_gene_id":"ENSG00000207025.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18395994,"end":18396095,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221456.1","gene_symbol":"MIR1202","gene_name":"microRNA 1202 [Source:HGNC Symbol;Acc:HGNC:35268]","synonyms":"MIRN1202,hsa-mir-1202","biotype":"miRNA","ncbi_id":"100302259","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155946797,"end":155946879,"strand":1,"description":"microRNA 1202 [Source:HGNC Symbol;Acc:HGNC:35268]"}, {"versioned_ensembl_gene_id":"ENSG00000207286.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":25287432,"end":25287533,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266668.1","gene_symbol":"MIR5692C2","gene_name":"microRNA 5692c-2 [Source:HGNC Symbol;Acc:HGNC:43448]","synonyms":"hsa-mir-5692c-2","biotype":"miRNA","ncbi_id":"100847017","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97964405,"end":97964481,"strand":-1,"description":"microRNA 5692c-2 [Source:HGNC Symbol;Acc:HGNC:43448]"}, {"versioned_ensembl_gene_id":"ENSG00000266548.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31563664,"end":31563765,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283386.1","gene_symbol":"MIR4659B","gene_name":"microRNA 4659b [Source:HGNC Symbol;Acc:HGNC:41530]","synonyms":"hsa-mir-4659b","biotype":"miRNA","ncbi_id":"100616372","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6745168,"end":6745240,"strand":-1,"description":"microRNA 4659b [Source:HGNC Symbol;Acc:HGNC:41530]"}, {"versioned_ensembl_gene_id":"ENSG00000201133.1","gene_symbol":"SNORA4","gene_name":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]","synonyms":"ACA4","biotype":"snoRNA","ncbi_id":"619568","summary":null,"start":50935350,"end":50935493,"strand":-1,"description":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]"}, {"versioned_ensembl_gene_id":"ENSG00000277785.1","gene_symbol":"SNORD116-21","gene_name":"small nucleolar RNA, C/D box 116-21 [Source:HGNC Symbol;Acc:HGNC:33087]","synonyms":"HBII-85-21","biotype":"snoRNA","ncbi_id":"100033432","summary":null,"start":25088804,"end":25088895,"strand":1,"description":"small nucleolar RNA, C/D box 116-21 [Source:HGNC Symbol;Acc:HGNC:33087]"}, {"versioned_ensembl_gene_id":"ENSG00000201136.1","gene_symbol":"RNU6-353P","gene_name":"RNA, U6 small nuclear 353, pseudogene [Source:HGNC Symbol;Acc:HGNC:47316]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479723","summary":null,"start":43702363,"end":43702470,"strand":1,"description":"RNA, U6 small nuclear 353, pseudogene [Source:HGNC Symbol;Acc:HGNC:47316]"}, {"versioned_ensembl_gene_id":"ENSG00000264840.1","gene_symbol":"RN7SL404P","gene_name":"RNA, 7SL, cytoplasmic 404, pseudogene [Source:HGNC Symbol;Acc:HGNC:46420]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479372","summary":null,"start":64871504,"end":64871784,"strand":-1,"description":"RNA, 7SL, cytoplasmic 404, pseudogene [Source:HGNC Symbol;Acc:HGNC:46420]"}, {"versioned_ensembl_gene_id":"ENSG00000222835.1","gene_symbol":"RNA5SP100","gene_name":"RNA, 5S ribosomal pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:42898]","synonyms":"RN5S100","biotype":"rRNA","ncbi_id":"106480755","summary":null,"start":91674857,"end":91674966,"strand":1,"description":"RNA, 5S ribosomal pseudogene 100 [Source:HGNC Symbol;Acc:HGNC:42898]"}, {"versioned_ensembl_gene_id":"ENSG00000266206.1","gene_symbol":"MIR3926-1","gene_name":"microRNA 3926-1 [Source:HGNC Symbol;Acc:HGNC:38959]","synonyms":"hsa-mir-3926-1","biotype":"miRNA","ncbi_id":"100500870","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12727232,"end":12727304,"strand":-1,"description":"microRNA 3926-1 [Source:HGNC Symbol;Acc:HGNC:38959]"}, {"versioned_ensembl_gene_id":"ENSG00000252062.1","gene_symbol":"RNU6-469P","gene_name":"RNA, U6 small nuclear 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:47432]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481327","summary":null,"start":84886386,"end":84886486,"strand":-1,"description":"RNA, U6 small nuclear 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:47432]"}, {"versioned_ensembl_gene_id":"ENSG00000265251.1","gene_symbol":"MIR4288","gene_name":"microRNA 4288 [Source:HGNC Symbol;Acc:HGNC:38203]","synonyms":"hsa-mir-4288","biotype":"miRNA","ncbi_id":"100422903","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28505116,"end":28505182,"strand":-1,"description":"microRNA 4288 [Source:HGNC Symbol;Acc:HGNC:38203]"}, {"versioned_ensembl_gene_id":"ENSG00000266627.2","gene_symbol":"RN7SL202P","gene_name":"RNA, 7SL, cytoplasmic 202, pseudogene [Source:HGNC Symbol;Acc:HGNC:46218]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479295","summary":null,"start":3920245,"end":3920506,"strand":-1,"description":"RNA, 7SL, cytoplasmic 202, pseudogene [Source:HGNC Symbol;Acc:HGNC:46218]"}, {"versioned_ensembl_gene_id":"ENSG00000206593.1","gene_symbol":"RNU6-47P","gene_name":"RNA, U6 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:34291]","synonyms":"RNU6-47","biotype":"snRNA","ncbi_id":"106480710","summary":null,"start":109014834,"end":109014940,"strand":-1,"description":"RNA, U6 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:34291]"}, {"versioned_ensembl_gene_id":"ENSG00000276479.1","gene_symbol":"MIR548AZ","gene_name":"microRNA 548az [Source:HGNC Symbol;Acc:HGNC:49981]","synonyms":"hsa-mir-548az","biotype":"miRNA","ncbi_id":"102466162","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119325171,"end":119325265,"strand":1,"description":"microRNA 548az [Source:HGNC Symbol;Acc:HGNC:49981]"}, {"versioned_ensembl_gene_id":"ENSG00000276598.1","gene_symbol":"MIR6893","gene_name":"microRNA 6893 [Source:HGNC Symbol;Acc:HGNC:50130]","synonyms":"hsa-mir-6893","biotype":"miRNA","ncbi_id":"102466271","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144435551,"end":144435619,"strand":-1,"description":"microRNA 6893 [Source:HGNC Symbol;Acc:HGNC:50130]"}, {"versioned_ensembl_gene_id":"ENSG00000222468.1","gene_symbol":"RNA5SP261","gene_name":"RNA, 5S ribosomal pseudogene 261 [Source:HGNC Symbol;Acc:HGNC:43161]","synonyms":"RN5S261","biotype":"rRNA","ncbi_id":"100873515","summary":null,"start":31598099,"end":31598204,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 261 [Source:HGNC Symbol;Acc:HGNC:43161]"}, {"versioned_ensembl_gene_id":"ENSG00000283242.1","gene_symbol":"MIR384","gene_name":"microRNA 384 [Source:HGNC Symbol;Acc:HGNC:31878]","synonyms":"MIRN384,hsa-mir-384","biotype":"miRNA","ncbi_id":"494333","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76919273,"end":76919360,"strand":-1,"description":"microRNA 384 [Source:HGNC Symbol;Acc:HGNC:31878]"}, {"versioned_ensembl_gene_id":"ENSG00000222267.1","gene_symbol":"RNU6-892P","gene_name":"RNA, U6 small nuclear 892, pseudogene [Source:HGNC Symbol;Acc:HGNC:47855]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481460","summary":null,"start":20229779,"end":20229877,"strand":1,"description":"RNA, U6 small nuclear 892, pseudogene [Source:HGNC Symbol;Acc:HGNC:47855]"}, {"versioned_ensembl_gene_id":"ENSG00000212559.1","gene_symbol":"RNA5SP35","gene_name":"RNA, 5S ribosomal pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:42611]","synonyms":"RN5S35","biotype":"rRNA","ncbi_id":"100873367","summary":null,"start":94025470,"end":94025598,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:42611]"}, {"versioned_ensembl_gene_id":"ENSG00000223300.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73858061,"end":73858165,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275014.1","gene_symbol":"RN7SL166P","gene_name":"RNA, 7SL, cytoplasmic 166, pseudogene [Source:HGNC Symbol;Acc:HGNC:46182]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479282","summary":null,"start":19736975,"end":19737254,"strand":-1,"description":"RNA, 7SL, cytoplasmic 166, pseudogene [Source:HGNC Symbol;Acc:HGNC:46182]"}, {"versioned_ensembl_gene_id":"ENSG00000202472.1","gene_symbol":"RNA5SP248","gene_name":"RNA, 5S ribosomal pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:43148]","synonyms":"RN5S248","biotype":"rRNA","ncbi_id":"100873504","summary":null,"start":140386781,"end":140386907,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 248 [Source:HGNC Symbol;Acc:HGNC:43148]"}, {"versioned_ensembl_gene_id":"ENSG00000222438.1","gene_symbol":"RNU6-1077P","gene_name":"RNA, U6 small nuclear 1077, pseudogene [Source:HGNC Symbol;Acc:HGNC:48040]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480039","summary":null,"start":130869736,"end":130869837,"strand":-1,"description":"RNA, U6 small nuclear 1077, pseudogene [Source:HGNC Symbol;Acc:HGNC:48040]"}, {"versioned_ensembl_gene_id":"ENSG00000199440.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":77821030,"end":77821142,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201196.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52852607,"end":52852703,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283034.1","gene_symbol":"ZNF445","gene_name":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]","synonyms":"ZSCAN47,ZNF168,ZKSCAN15","biotype":"protein_coding","ncbi_id":"353274","summary":null,"start":44431720,"end":44477670,"strand":-1,"description":"zinc finger protein 445 [Source:HGNC Symbol;Acc:HGNC:21018]"}, {"versioned_ensembl_gene_id":"ENSG00000202523.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":83992932,"end":83993033,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252089.1","gene_symbol":"RNU4ATAC7P","gene_name":"RNA, U4atac small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:46893]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480539","summary":null,"start":54859688,"end":54859812,"strand":-1,"description":"RNA, U4atac small nuclear 7, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252987.1","gene_symbol":"RNA5SP66","gene_name":"RNA, 5S ribosomal pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:42843]","synonyms":"RN5S66","biotype":"rRNA","ncbi_id":"100873301","summary":null,"start":169067264,"end":169067364,"strand":1,"description":"RNA, 5S ribosomal pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:42843]"}, {"versioned_ensembl_gene_id":"ENSG00000252768.1","gene_symbol":"RNU6-856P","gene_name":"RNA, U6 small nuclear 856, pseudogene [Source:HGNC Symbol;Acc:HGNC:47819]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481451","summary":null,"start":52551846,"end":52551943,"strand":-1,"description":"RNA, U6 small nuclear 856, pseudogene [Source:HGNC Symbol;Acc:HGNC:47819]"}, {"versioned_ensembl_gene_id":"ENSG00000239710.3","gene_symbol":"RN7SL692P","gene_name":"RNA, 7SL, cytoplasmic 692, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000279767.1","gene_symbol":"AL513523.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":153772371,"end":153774079,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000238825.1","gene_symbol":"RNU1-13P","gene_name":"RNA, U1 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:10138]","synonyms":"U1P1,U1.1,RNU1P6","biotype":"snRNA","ncbi_id":"26860","summary":null,"start":148388490,"end":148388651,"strand":-1,"description":"RNA, U1 small nuclear 13, pseudogene [Source:HGNC Symbol;Acc:HGNC:10138]"}, {"versioned_ensembl_gene_id":"ENSG00000201180.1","gene_symbol":"RNU6-115P","gene_name":"RNA, U6 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:47078]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479617","summary":null,"start":15022852,"end":15022958,"strand":1,"description":"RNA, U6 small nuclear 115, pseudogene [Source:HGNC Symbol;Acc:HGNC:47078]"}, {"versioned_ensembl_gene_id":"ENSG00000206774.1","gene_symbol":"RNU6-211P","gene_name":"RNA, U6 small nuclear 211, pseudogene [Source:HGNC Symbol;Acc:HGNC:47174]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479660","summary":null,"start":80365726,"end":80365832,"strand":-1,"description":"RNA, U6 small nuclear 211, pseudogene [Source:HGNC Symbol;Acc:HGNC:47174]"}, {"versioned_ensembl_gene_id":"ENSG00000275961.1","gene_symbol":"RN7SL210P","gene_name":"RNA, 7SL, cytoplasmic 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:46226]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479298","summary":null,"start":96004563,"end":96004850,"strand":-1,"description":"RNA, 7SL, cytoplasmic 210, pseudogene [Source:HGNC Symbol;Acc:HGNC:46226]"}, {"versioned_ensembl_gene_id":"ENSG00000263675.1","gene_symbol":"MIR5581","gene_name":"microRNA 5581 [Source:HGNC Symbol;Acc:HGNC:43527]","synonyms":"hsa-mir-5581","biotype":"miRNA","ncbi_id":"100847010","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37500935,"end":37500994,"strand":-1,"description":"microRNA 5581 [Source:HGNC Symbol;Acc:HGNC:43527]"}, {"versioned_ensembl_gene_id":"ENSG00000223198.1","gene_symbol":"RNU2-22P","gene_name":"RNA, U2 small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:48515]","synonyms":null,"biotype":"snRNA","ncbi_id":"106660611","summary":null,"start":231501990,"end":231502201,"strand":-1,"description":"RNA, U2 small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:48515]"}, {"versioned_ensembl_gene_id":"ENSG00000238835.1","gene_symbol":"SCARNA18","gene_name":"small Cajal body-specific RNA 18 [Source:HGNC Symbol;Acc:HGNC:32559]","synonyms":"U109,SCARNA18A","biotype":"snoRNA","ncbi_id":"677765","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":83064204,"end":83064337,"strand":-1,"description":"small Cajal body-specific RNA 18 [Source:HGNC Symbol;Acc:HGNC:32559]"}, {"versioned_ensembl_gene_id":"ENSG00000201447.1","gene_symbol":"RNA5SP509","gene_name":"RNA, 5S ribosomal pseudogene 509 [Source:HGNC Symbol;Acc:HGNC:43409]","synonyms":"RN5S509","biotype":"rRNA","ncbi_id":"100873560","summary":null,"start":77066709,"end":77066827,"strand":1,"description":"RNA, 5S ribosomal pseudogene 509 [Source:HGNC Symbol;Acc:HGNC:43409]"}, {"versioned_ensembl_gene_id":"ENSG00000284202.1","gene_symbol":"MIR137","gene_name":"microRNA 137 [Source:HGNC Symbol;Acc:HGNC:31523]","synonyms":"MIRN137,miR-137,hsa-mir-137","biotype":"miRNA","ncbi_id":"406928","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98046070,"end":98046171,"strand":-1,"description":"microRNA 137 [Source:HGNC Symbol;Acc:HGNC:31523]"}, {"versioned_ensembl_gene_id":"ENSG00000200051.1","gene_symbol":"SNORD45","gene_name":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":140527352,"end":140527428,"strand":-1,"description":"Small nucleolar RNA SNORD45 [Source:RFAM;Acc:RF00279]"}, {"versioned_ensembl_gene_id":"ENSG00000253097.1","gene_symbol":"RNU2-19P","gene_name":"RNA, U2 small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:48512]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481959","summary":null,"start":205566716,"end":205566799,"strand":1,"description":"RNA, U2 small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:48512]"}, {"versioned_ensembl_gene_id":"ENSG00000222831.1","gene_symbol":"MIR1537","gene_name":"microRNA 1537 [Source:HGNC Symbol;Acc:HGNC:35381]","synonyms":"hsa-mir-1537,MIRN1537","biotype":"miRNA","ncbi_id":"100302139","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":235853000,"end":235853060,"strand":-1,"description":"microRNA 1537 [Source:HGNC Symbol;Acc:HGNC:35381]"}, {"versioned_ensembl_gene_id":"ENSG00000201749.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":114615455,"end":114615568,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283672.1","gene_symbol":"MIR4678","gene_name":"microRNA 4678 [Source:HGNC Symbol;Acc:HGNC:41717]","synonyms":"hsa-mir-4678","biotype":"miRNA","ncbi_id":"100616296","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":87503881,"end":87503954,"strand":1,"description":"microRNA 4678 [Source:HGNC Symbol;Acc:HGNC:41717]"}, {"versioned_ensembl_gene_id":"ENSG00000201239.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":82417226,"end":82417321,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265727.2","gene_symbol":"RN7SL648P","gene_name":"RNA, 7SL, cytoplasmic 648, pseudogene [Source:HGNC Symbol;Acc:HGNC:46664]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479459","summary":null,"start":74242608,"end":74242908,"strand":-1,"description":"RNA, 7SL, cytoplasmic 648, pseudogene [Source:HGNC Symbol;Acc:HGNC:46664]"}, {"versioned_ensembl_gene_id":"ENSG00000221214.1","gene_symbol":"MIR548E","gene_name":"microRNA 548e [Source:HGNC Symbol;Acc:HGNC:35275]","synonyms":"MIRN548E,hsa-mir-548e","biotype":"miRNA","ncbi_id":"100313921","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110988926,"end":110989013,"strand":1,"description":"microRNA 548e [Source:HGNC Symbol;Acc:HGNC:35275]"}, {"versioned_ensembl_gene_id":"ENSG00000201882.1","gene_symbol":"snoU2-30","gene_name":"Small nucleolar RNA U2-30 [Source:RFAM;Acc:RF00493]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":20136066,"end":20136135,"strand":-1,"description":"Small nucleolar RNA U2-30 [Source:RFAM;Acc:RF00493]"}, {"versioned_ensembl_gene_id":"ENSG00000266581.1","gene_symbol":"MIR3166","gene_name":"microRNA 3166 [Source:HGNC Symbol;Acc:HGNC:38386]","synonyms":"hsa-mir-3166","biotype":"miRNA","ncbi_id":"100423040","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88176502,"end":88176593,"strand":1,"description":"microRNA 3166 [Source:HGNC Symbol;Acc:HGNC:38386]"}, {"versioned_ensembl_gene_id":"ENSG00000200304.1","gene_symbol":"RNU6-1255P","gene_name":"RNA, U6 small nuclear 1255, pseudogene [Source:HGNC Symbol;Acc:HGNC:48218]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481946","summary":null,"start":130069541,"end":130069652,"strand":-1,"description":"RNA, U6 small nuclear 1255, pseudogene [Source:HGNC Symbol;Acc:HGNC:48218]"}, {"versioned_ensembl_gene_id":"ENSG00000201633.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":83636196,"end":83636290,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201807.1","gene_symbol":"SNORA27","gene_name":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]","synonyms":"ACA27","biotype":"snoRNA","ncbi_id":"619499","summary":null,"start":136855698,"end":136855831,"strand":-1,"description":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]"}, {"versioned_ensembl_gene_id":"ENSG00000238764.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":17357930,"end":17358033,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000215991.1","gene_symbol":"MIR208B","gene_name":"microRNA 208b [Source:HGNC Symbol;Acc:HGNC:33669]","synonyms":"MIRN208B,hsa-mir-208b","biotype":"miRNA","ncbi_id":"100126336","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23417987,"end":23418063,"strand":-1,"description":"microRNA 208b [Source:HGNC Symbol;Acc:HGNC:33669]"}, {"versioned_ensembl_gene_id":"ENSG00000215957.1","gene_symbol":"MIR300","gene_name":"microRNA 300 [Source:HGNC Symbol;Acc:HGNC:33636]","synonyms":"hsa-mir-300,MIRN300","biotype":"miRNA","ncbi_id":"100126297","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101041363,"end":101041445,"strand":1,"description":"microRNA 300 [Source:HGNC Symbol;Acc:HGNC:33636]"}, {"versioned_ensembl_gene_id":"ENSG00000251954.1","gene_symbol":"RNU6-496P","gene_name":"RNA, U6 small nuclear 496, pseudogene [Source:HGNC Symbol;Acc:HGNC:47459]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480584","summary":null,"start":111421510,"end":111421608,"strand":-1,"description":"RNA, U6 small nuclear 496, pseudogene [Source:HGNC Symbol;Acc:HGNC:47459]"}, {"versioned_ensembl_gene_id":"ENSG00000221641.1","gene_symbol":"MIR1268A","gene_name":"microRNA 1268a [Source:HGNC Symbol;Acc:HGNC:35336]","synonyms":"MIRN1268,MIR1268,hsa-mir-1268","biotype":"miRNA","ncbi_id":"100302233","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22225278,"end":22225329,"strand":-1,"description":"microRNA 1268a [Source:HGNC Symbol;Acc:HGNC:35336]"}, {"versioned_ensembl_gene_id":"ENSG00000207282.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18113467,"end":18113579,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222205.1","gene_symbol":"RNA5SP266","gene_name":"RNA, 5S ribosomal pseudogene 266 [Source:HGNC Symbol;Acc:HGNC:43166]","synonyms":"RN5S266","biotype":"rRNA","ncbi_id":"100873519","summary":null,"start":57126655,"end":57126762,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 266 [Source:HGNC Symbol;Acc:HGNC:43166]"}, {"versioned_ensembl_gene_id":"ENSG00000273613.1","gene_symbol":"MIR6511A4","gene_name":"microRNA 6511a-4 [Source:HGNC Symbol;Acc:HGNC:50188]","synonyms":"hsa-mir-6511a-4","biotype":"miRNA","ncbi_id":"102465684","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18344013,"end":18344079,"strand":-1,"description":"microRNA 6511a-4 [Source:HGNC Symbol;Acc:HGNC:50188]"}, {"versioned_ensembl_gene_id":"ENSG00000238886.1","gene_symbol":"SNORD121A","gene_name":"small nucleolar RNA, C/D box 121A [Source:HGNC Symbol;Acc:HGNC:33560]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113379","summary":null,"start":33952769,"end":33952850,"strand":-1,"description":"small nucleolar RNA, C/D box 121A [Source:HGNC Symbol;Acc:HGNC:33560]"}, {"versioned_ensembl_gene_id":"ENSG00000275429.1","gene_symbol":"MIR6862-1","gene_name":"microRNA 6862-1 [Source:HGNC Symbol;Acc:HGNC:50052]","synonyms":"hsa-mir-6862-1","biotype":"miRNA","ncbi_id":"102465520","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28390982,"end":28391051,"strand":-1,"description":"microRNA 6862-1 [Source:HGNC Symbol;Acc:HGNC:50052]"}, {"versioned_ensembl_gene_id":"ENSG00000273966.1","gene_symbol":"pRNA","gene_name":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17568962,"end":17569051,"strand":-1,"description":"NoRC assoicated RNA, pRNA [Source:RFAM;Acc:RF01518]"}, {"versioned_ensembl_gene_id":"ENSG00000254341.2","gene_symbol":"SNORD87","gene_name":"small nucleolar RNA, C/D box 87 [Source:HGNC Symbol;Acc:HGNC:32746]","synonyms":"U87,HBII-276","biotype":"snoRNA","ncbi_id":"641648","summary":"Small nucleolar RNAs (snoRNAs) of the C/D class, such as SNORD87, are involved in 2-prime-methylation of preribosomal RNA precursors (Gogolevskaya et al., 2002 [PubMed 12119114]).[supplied by OMIM, Aug 2008]","start":66922467,"end":66922555,"strand":-1,"description":"small nucleolar RNA, C/D box 87 [Source:HGNC Symbol;Acc:HGNC:32746]"}, {"versioned_ensembl_gene_id":"ENSG00000242893.3","gene_symbol":"RN7SL413P","gene_name":"RNA, 7SL, cytoplasmic 413, pseudogene [Source:HGNC Symbol;Acc:HGNC:46429]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479374","summary":null,"start":51593919,"end":51594215,"strand":-1,"description":"RNA, 7SL, cytoplasmic 413, pseudogene [Source:HGNC Symbol;Acc:HGNC:46429]"}, {"versioned_ensembl_gene_id":"ENSG00000242650.3","gene_symbol":"RN7SL292P","gene_name":"RNA, 7SL, cytoplasmic 292, pseudogene [Source:HGNC Symbol;Acc:HGNC:46308]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481002","summary":null,"start":51716657,"end":51716922,"strand":1,"description":"RNA, 7SL, cytoplasmic 292, pseudogene [Source:HGNC Symbol;Acc:HGNC:46308]"}, {"versioned_ensembl_gene_id":"ENSG00000266305.1","gene_symbol":"MIR4518","gene_name":"microRNA 4518 [Source:HGNC Symbol;Acc:HGNC:41809]","synonyms":"hsa-mir-4518","biotype":"miRNA","ncbi_id":"100616405","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30503919,"end":30504001,"strand":1,"description":"microRNA 4518 [Source:HGNC Symbol;Acc:HGNC:41809]"}, {"versioned_ensembl_gene_id":"ENSG00000240964.3","gene_symbol":"RN7SL751P","gene_name":"RNA, 7SL, cytoplasmic 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:46767]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479495","summary":null,"start":78938009,"end":78938292,"strand":-1,"description":"RNA, 7SL, cytoplasmic 751, pseudogene [Source:HGNC Symbol;Acc:HGNC:46767]"}, {"versioned_ensembl_gene_id":"ENSG00000238875.1","gene_symbol":"RN7SKP210","gene_name":"RNA, 7SK small nuclear pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:45934]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480898","summary":null,"start":39874255,"end":39874515,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 210 [Source:HGNC Symbol;Acc:HGNC:45934]"}, {"versioned_ensembl_gene_id":"ENSG00000200788.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127470875,"end":127470987,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274134.1","gene_symbol":"MIR6774","gene_name":"microRNA 6774 [Source:HGNC Symbol;Acc:HGNC:50202]","synonyms":"hsa-mir-6774","biotype":"miRNA","ncbi_id":"102466732","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85918347,"end":85918416,"strand":1,"description":"microRNA 6774 [Source:HGNC Symbol;Acc:HGNC:50202]"}, {"versioned_ensembl_gene_id":"ENSG00000252521.1","gene_symbol":"RNU5D-2P","gene_name":"RNA, U5D small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42534]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873841","summary":null,"start":132421641,"end":132421690,"strand":1,"description":"RNA, U5D small nuclear 2, pseudogene [Source:HGNC Symbol;Acc:HGNC:42534]"}, {"versioned_ensembl_gene_id":"ENSG00000199031.1","gene_symbol":"MIR371A","gene_name":"microRNA 371a [Source:HGNC Symbol;Acc:HGNC:31785]","synonyms":"MIRN371,MIR371,hsa-mir-371","biotype":"miRNA","ncbi_id":"442916","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53787675,"end":53787741,"strand":1,"description":"microRNA 371a [Source:HGNC Symbol;Acc:HGNC:31785]"}, {"versioned_ensembl_gene_id":"ENSG00000252079.1","gene_symbol":"RNU6-327P","gene_name":"RNA, U6 small nuclear 327, pseudogene [Source:HGNC Symbol;Acc:HGNC:47290]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481887","summary":null,"start":132835374,"end":132835500,"strand":-1,"description":"RNA, U6 small nuclear 327, pseudogene [Source:HGNC Symbol;Acc:HGNC:47290]"}, {"versioned_ensembl_gene_id":"ENSG00000273555.1","gene_symbol":"MIR6812","gene_name":"microRNA 6812 [Source:HGNC Symbol;Acc:HGNC:50116]","synonyms":"hsa-mir-6812","biotype":"miRNA","ncbi_id":"102465487","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45425510,"end":45425573,"strand":1,"description":"microRNA 6812 [Source:HGNC Symbol;Acc:HGNC:50116]"}, {"versioned_ensembl_gene_id":"ENSG00000252601.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":29070496,"end":29070610,"strand":1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000264824.1","gene_symbol":"MIR5571","gene_name":"microRNA 5571 [Source:HGNC Symbol;Acc:HGNC:43513]","synonyms":"hsa-mir-5571","biotype":"miRNA","ncbi_id":"100847006","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22886267,"end":22886379,"strand":1,"description":"microRNA 5571 [Source:HGNC Symbol;Acc:HGNC:43513]"}, {"versioned_ensembl_gene_id":"ENSG00000207369.1","gene_symbol":"RNU6-665P","gene_name":"RNA, U6 small nuclear 665, pseudogene [Source:HGNC Symbol;Acc:HGNC:47628]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481392","summary":null,"start":47667771,"end":47667877,"strand":1,"description":"RNA, U6 small nuclear 665, pseudogene [Source:HGNC Symbol;Acc:HGNC:47628]"}, {"versioned_ensembl_gene_id":"ENSG00000280004.1","gene_symbol":"AC005086.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":102186819,"end":102187039,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241074.3","gene_symbol":"RN7SL813P","gene_name":"RNA, 7SL, cytoplasmic 813, pseudogene [Source:HGNC Symbol;Acc:HGNC:46829]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480534","summary":null,"start":168451324,"end":168451606,"strand":1,"description":"RNA, 7SL, cytoplasmic 813, pseudogene [Source:HGNC Symbol;Acc:HGNC:46829]"}, {"versioned_ensembl_gene_id":"ENSG00000199595.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":161699506,"end":161699607,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265483.1","gene_symbol":"MIR4443","gene_name":"microRNA 4443 [Source:HGNC Symbol;Acc:HGNC:41830]","synonyms":"hsa-mir-4443","biotype":"miRNA","ncbi_id":"100616407","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48196564,"end":48196616,"strand":1,"description":"microRNA 4443 [Source:HGNC Symbol;Acc:HGNC:41830]"}, {"versioned_ensembl_gene_id":"ENSG00000272337.1","gene_symbol":"RNU6-90P","gene_name":"RNA, U6 small nuclear 90, pseudogene [Source:HGNC Symbol;Acc:HGNC:47053]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481205","summary":null,"start":51907200,"end":51907305,"strand":1,"description":"RNA, U6 small nuclear 90, pseudogene [Source:HGNC Symbol;Acc:HGNC:47053]"}, {"versioned_ensembl_gene_id":"ENSG00000264330.1","gene_symbol":"MIR5186","gene_name":"microRNA 5186 [Source:HGNC Symbol;Acc:HGNC:43459]","synonyms":"hsa-mir-5186","biotype":"miRNA","ncbi_id":"100847036","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151565876,"end":151565995,"strand":-1,"description":"microRNA 5186 [Source:HGNC Symbol;Acc:HGNC:43459]"}, {"versioned_ensembl_gene_id":"ENSG00000240869.3","gene_symbol":"RN7SL128P","gene_name":"RNA, 7SL, cytoplasmic 128, pseudogene [Source:HGNC Symbol;Acc:HGNC:46144]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481826","summary":null,"start":20421583,"end":20421887,"strand":-1,"description":"RNA, 7SL, cytoplasmic 128, pseudogene [Source:HGNC Symbol;Acc:HGNC:46144]"}, {"versioned_ensembl_gene_id":"ENSG00000265606.1","gene_symbol":"MIR4695","gene_name":"microRNA 4695 [Source:HGNC Symbol;Acc:HGNC:41573]","synonyms":"hsa-mir-4695","biotype":"miRNA","ncbi_id":"100616120","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18883202,"end":18883275,"strand":-1,"description":"microRNA 4695 [Source:HGNC Symbol;Acc:HGNC:41573]"}, {"versioned_ensembl_gene_id":"ENSG00000207717.1","gene_symbol":"MIR551B","gene_name":"microRNA 551b [Source:HGNC Symbol;Acc:HGNC:32807]","synonyms":"MIRN551B,hsa-mir-551b","biotype":"miRNA","ncbi_id":"693136","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168551854,"end":168551949,"strand":1,"description":"microRNA 551b [Source:HGNC Symbol;Acc:HGNC:32807]"}, {"versioned_ensembl_gene_id":"ENSG00000207240.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31382317,"end":31382430,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238933.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":61642383,"end":61642494,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284276.1","gene_symbol":"MIR4800","gene_name":"microRNA 4800 [Source:HGNC Symbol;Acc:HGNC:41877]","synonyms":"hsa-mir-4800","biotype":"miRNA","ncbi_id":"100616358","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2250077,"end":2250156,"strand":-1,"description":"microRNA 4800 [Source:HGNC Symbol;Acc:HGNC:41877]"}, {"versioned_ensembl_gene_id":"ENSG00000252892.1","gene_symbol":"RNU6-548P","gene_name":"RNA, U6 small nuclear 548, pseudogene [Source:HGNC Symbol;Acc:HGNC:47511]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481354","summary":null,"start":64994746,"end":64994860,"strand":1,"description":"RNA, U6 small nuclear 548, pseudogene [Source:HGNC Symbol;Acc:HGNC:47511]"}, {"versioned_ensembl_gene_id":"ENSG00000199674.1","gene_symbol":"RNU6-862P","gene_name":"RNA, U6 small nuclear 862, pseudogene [Source:HGNC Symbol;Acc:HGNC:47825]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481920","summary":null,"start":16137768,"end":16137872,"strand":-1,"description":"RNA, U6 small nuclear 862, pseudogene [Source:HGNC Symbol;Acc:HGNC:47825]"}, {"versioned_ensembl_gene_id":"ENSG00000252486.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27252119,"end":27252235,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221676.1","gene_symbol":"RNU6ATAC","gene_name":"RNA, U6atac small nuclear (U12-dependent splicing) [Source:HGNC Symbol;Acc:HGNC:34017]","synonyms":"RNU6ATAC1","biotype":"snRNA","ncbi_id":"100151684","summary":null,"start":134164439,"end":134164564,"strand":-1,"description":"RNA, U6atac small nuclear (U12-dependent splicing) [Source:HGNC Symbol;Acc:HGNC:34017]"}, {"versioned_ensembl_gene_id":"ENSG00000252746.1","gene_symbol":"RNU6-273P","gene_name":"RNA, U6 small nuclear 273, pseudogene [Source:HGNC Symbol;Acc:HGNC:47236]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480566","summary":null,"start":37187219,"end":37187314,"strand":1,"description":"RNA, U6 small nuclear 273, pseudogene [Source:HGNC Symbol;Acc:HGNC:47236]"}, {"versioned_ensembl_gene_id":"ENSG00000284443.1","gene_symbol":"MIR197","gene_name":"microRNA 197 [Source:HGNC Symbol;Acc:HGNC:31569]","synonyms":"MIRN197,hsa-mir-197","biotype":"miRNA","ncbi_id":"406974","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109598893,"end":109598967,"strand":1,"description":"microRNA 197 [Source:HGNC Symbol;Acc:HGNC:31569]"}, {"versioned_ensembl_gene_id":"ENSG00000263642.1","gene_symbol":"MIR4802","gene_name":"microRNA 4802 [Source:HGNC Symbol;Acc:HGNC:41658]","synonyms":"hsa-mir-4802","biotype":"miRNA","ncbi_id":"100616274","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40502040,"end":40502119,"strand":-1,"description":"microRNA 4802 [Source:HGNC Symbol;Acc:HGNC:41658]"}, {"versioned_ensembl_gene_id":"ENSG00000202229.1","gene_symbol":"RNU6-1138P","gene_name":"RNA, U6 small nuclear 1138, pseudogene [Source:HGNC Symbol;Acc:HGNC:48101]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480641","summary":null,"start":23156309,"end":23156414,"strand":-1,"description":"RNA, U6 small nuclear 1138, pseudogene [Source:HGNC Symbol;Acc:HGNC:48101]"}, {"versioned_ensembl_gene_id":"ENSG00000275667.1","gene_symbol":"MIR6839","gene_name":"microRNA 6839 [Source:HGNC Symbol;Acc:HGNC:49953]","synonyms":"hsa-mir-6839","biotype":"miRNA","ncbi_id":"102465505","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64679064,"end":64679176,"strand":1,"description":"microRNA 6839 [Source:HGNC Symbol;Acc:HGNC:49953]"}, {"versioned_ensembl_gene_id":"ENSG00000239093.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":187423315,"end":187423419,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000199059.3","gene_symbol":"MIR135B","gene_name":"microRNA 135b [Source:HGNC Symbol;Acc:HGNC:31760]","synonyms":"MIRN135B,hsa-mir-135b","biotype":"miRNA","ncbi_id":"442891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":205448302,"end":205448398,"strand":-1,"description":"microRNA 135b [Source:HGNC Symbol;Acc:HGNC:31760]"}, {"versioned_ensembl_gene_id":"ENSG00000252013.1","gene_symbol":"RNU4ATAC14P","gene_name":"RNA, U4atac small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46900]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481159","summary":null,"start":75202081,"end":75202169,"strand":-1,"description":"RNA, U4atac small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46900]"}, {"versioned_ensembl_gene_id":"ENSG00000276211.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":54942736,"end":54967295,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000266756.1","gene_symbol":"MIR5680","gene_name":"microRNA 5680 [Source:HGNC Symbol;Acc:HGNC:43492]","synonyms":"hsa-mir-5680","biotype":"miRNA","ncbi_id":"100847001","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102125432,"end":102125515,"strand":1,"description":"microRNA 5680 [Source:HGNC Symbol;Acc:HGNC:43492]"}, {"versioned_ensembl_gene_id":"ENSG00000275662.1","gene_symbol":"SNORD112","gene_name":"small nucleolar RNA, C/D box 112 [Source:HGNC Symbol;Acc:HGNC:32777]","synonyms":"14q(0)","biotype":"snoRNA","ncbi_id":"692215","summary":"Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]","start":100897920,"end":100897996,"strand":1,"description":"small nucleolar RNA, C/D box 112 [Source:HGNC Symbol;Acc:HGNC:32777]"}, {"versioned_ensembl_gene_id":"ENSG00000283435.1","gene_symbol":"MIR1321","gene_name":"microRNA 1321 [Source:HGNC Symbol;Acc:HGNC:35373]","synonyms":"hsa-mir-1321,MIRN1321","biotype":"miRNA","ncbi_id":"100302171","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85835780,"end":85835858,"strand":1,"description":"microRNA 1321 [Source:HGNC Symbol;Acc:HGNC:35373]"}, {"versioned_ensembl_gene_id":"ENSG00000278778.1","gene_symbol":"HTT-AS1_1","gene_name":"HTT antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02134]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":3063472,"end":3063701,"strand":1,"description":"HTT antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02134]"}, {"versioned_ensembl_gene_id":"ENSG00000263744.1","gene_symbol":"MIR3664","gene_name":"microRNA 3664 [Source:HGNC Symbol;Acc:HGNC:38899]","synonyms":"hsa-mir-3664","biotype":"miRNA","ncbi_id":"100500844","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70872270,"end":70872368,"strand":-1,"description":"microRNA 3664 [Source:HGNC Symbol;Acc:HGNC:38899]"}, {"versioned_ensembl_gene_id":"ENSG00000284043.1","gene_symbol":"MIR20B","gene_name":"microRNA 20b [Source:HGNC Symbol;Acc:HGNC:32024]","synonyms":"MIRN20B,hsa-mir-20b","biotype":"miRNA","ncbi_id":"574032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134169809,"end":134169877,"strand":-1,"description":"microRNA 20b [Source:HGNC Symbol;Acc:HGNC:32024]"}, {"versioned_ensembl_gene_id":"ENSG00000200463.1","gene_symbol":"SNORD118","gene_name":"small nucleolar RNA, C/D box 118 [Source:HGNC Symbol;Acc:HGNC:32952]","synonyms":"U8","biotype":"snoRNA","ncbi_id":"727676","summary":null,"start":8173454,"end":8173587,"strand":-1,"description":"small nucleolar RNA, C/D box 118 [Source:HGNC Symbol;Acc:HGNC:32952]"}, {"versioned_ensembl_gene_id":"ENSG00000200887.1","gene_symbol":"RNU6-598P","gene_name":"RNA, U6 small nuclear 598, pseudogene [Source:HGNC Symbol;Acc:HGNC:47561]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479830","summary":null,"start":30299569,"end":30299673,"strand":-1,"description":"RNA, U6 small nuclear 598, pseudogene [Source:HGNC Symbol;Acc:HGNC:47561]"}, {"versioned_ensembl_gene_id":"ENSG00000252454.3","gene_symbol":"MIR2114","gene_name":"microRNA 2114 [Source:HGNC Symbol;Acc:HGNC:37308]","synonyms":"hsa-mir-2114","biotype":"miRNA","ncbi_id":"100313839","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":150228004,"end":150228083,"strand":1,"description":"microRNA 2114 [Source:HGNC Symbol;Acc:HGNC:37308]"}, {"versioned_ensembl_gene_id":"ENSG00000264211.1","gene_symbol":"MIR4492","gene_name":"microRNA 4492 [Source:HGNC Symbol;Acc:HGNC:41563]","synonyms":"hsa-mir-4492","biotype":"miRNA","ncbi_id":"100616376","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":118910708,"end":118910787,"strand":1,"description":"microRNA 4492 [Source:HGNC Symbol;Acc:HGNC:41563]"}, {"versioned_ensembl_gene_id":"ENSG00000200661.1","gene_symbol":"SNORD116-10","gene_name":"small nucleolar RNA, C/D box 116-10 [Source:HGNC Symbol;Acc:HGNC:33076]","synonyms":"HBII-85-10","biotype":"snoRNA","ncbi_id":"100033422","summary":null,"start":25074114,"end":25074215,"strand":1,"description":"small nucleolar RNA, C/D box 116-10 [Source:HGNC Symbol;Acc:HGNC:33076]"}, {"versioned_ensembl_gene_id":"ENSG00000284450.1","gene_symbol":"MIR664B","gene_name":"microRNA 664b [Source:HGNC Symbol;Acc:HGNC:43501]","synonyms":"MIR644B,hsa-mir-664b","biotype":"miRNA","ncbi_id":"100847052","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154768596,"end":154768656,"strand":1,"description":"microRNA 664b [Source:HGNC Symbol;Acc:HGNC:43501]"}, {"versioned_ensembl_gene_id":"ENSG00000221604.1","gene_symbol":"MIR1293","gene_name":"microRNA 1293 [Source:HGNC Symbol;Acc:HGNC:35286]","synonyms":"MIRN1293,hsa-mir-1293","biotype":"miRNA","ncbi_id":"100302220","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50234142,"end":50234212,"strand":-1,"description":"microRNA 1293 [Source:HGNC Symbol;Acc:HGNC:35286]"}, {"versioned_ensembl_gene_id":"ENSG00000222976.1","gene_symbol":"RN7SKP94","gene_name":"RNA, 7SK small nuclear pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:45818]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480365","summary":null,"start":57789449,"end":57789732,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 94 [Source:HGNC Symbol;Acc:HGNC:45818]"}, {"versioned_ensembl_gene_id":"ENSG00000276138.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":15273855,"end":15273961,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000271932.1","gene_symbol":"RNU6-85P","gene_name":"RNA, U6 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47048]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481203","summary":null,"start":140884072,"end":140884178,"strand":1,"description":"RNA, U6 small nuclear 85, pseudogene [Source:HGNC Symbol;Acc:HGNC:47048]"}, {"versioned_ensembl_gene_id":"ENSG00000283487.1","gene_symbol":"MIR4501","gene_name":"microRNA 4501 [Source:HGNC Symbol;Acc:HGNC:41650]","synonyms":"hsa-mir-4501","biotype":"miRNA","ncbi_id":"100616137","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96427229,"end":96427292,"strand":1,"description":"microRNA 4501 [Source:HGNC Symbol;Acc:HGNC:41650]"}, {"versioned_ensembl_gene_id":"ENSG00000277262.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31107692,"end":31107794,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000276730.1","gene_symbol":"Hammerhead_HH9","gene_name":"Hammerhead ribozyme HH9 [Source:RFAM;Acc:RF02275]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36072686,"end":36072762,"strand":1,"description":"Hammerhead ribozyme HH9 [Source:RFAM;Acc:RF02275]"}, {"versioned_ensembl_gene_id":"ENSG00000263629.1","gene_symbol":"MIR5586","gene_name":"microRNA 5586 [Source:HGNC Symbol;Acc:HGNC:43493]","synonyms":"hsa-mir-5586","biotype":"miRNA","ncbi_id":"100847088","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59646962,"end":59647020,"strand":-1,"description":"microRNA 5586 [Source:HGNC Symbol;Acc:HGNC:43493]"}, {"versioned_ensembl_gene_id":"ENSG00000264646.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747504,"end":29747605,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239021.1","gene_symbol":"RNA5SP246","gene_name":"RNA, 5S ribosomal pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:43146]","synonyms":"RN5S246","biotype":"rRNA","ncbi_id":"100873502","summary":null,"start":130602795,"end":130602913,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 246 [Source:HGNC Symbol;Acc:HGNC:43146]"}, {"versioned_ensembl_gene_id":"ENSG00000277460.1","gene_symbol":"TTC28-AS1_1","gene_name":"TTC28 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02198]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27919384,"end":27919545,"strand":1,"description":"TTC28 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02198]"}, {"versioned_ensembl_gene_id":"ENSG00000264210.1","gene_symbol":"MIR4716","gene_name":"microRNA 4716 [Source:HGNC Symbol;Acc:HGNC:41812]","synonyms":"hsa-mir-4716","biotype":"miRNA","ncbi_id":"100616332","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49169070,"end":49169153,"strand":-1,"description":"microRNA 4716 [Source:HGNC Symbol;Acc:HGNC:41812]"}, {"versioned_ensembl_gene_id":"ENSG00000206671.1","gene_symbol":"RNU6-471P","gene_name":"RNA, U6 small nuclear 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:47434]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479774","summary":null,"start":27596412,"end":27596517,"strand":1,"description":"RNA, U6 small nuclear 471, pseudogene [Source:HGNC Symbol;Acc:HGNC:47434]"}, {"versioned_ensembl_gene_id":"ENSG00000222432.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":77895880,"end":77895992,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201095.1","gene_symbol":"RNU6-266P","gene_name":"RNA, U6 small nuclear 266, pseudogene [Source:HGNC Symbol;Acc:HGNC:47229]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479684","summary":null,"start":22527835,"end":22527941,"strand":1,"description":"RNA, U6 small nuclear 266, pseudogene [Source:HGNC Symbol;Acc:HGNC:47229]"}, {"versioned_ensembl_gene_id":"ENSG00000200293.1","gene_symbol":"RNA5SP393","gene_name":"RNA, 5S ribosomal pseudogene 393 [Source:HGNC Symbol;Acc:HGNC:43293]","synonyms":"RN5S393","biotype":"rRNA","ncbi_id":"100873646","summary":null,"start":41851913,"end":41852029,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 393 [Source:HGNC Symbol;Acc:HGNC:43293]"}, {"versioned_ensembl_gene_id":"ENSG00000276562.1","gene_symbol":"RN7SL565P","gene_name":"RNA, 7SL, cytoplasmic 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:46581]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481076","summary":null,"start":41578903,"end":41579186,"strand":1,"description":"RNA, 7SL, cytoplasmic 565, pseudogene [Source:HGNC Symbol;Acc:HGNC:46581]"}, {"versioned_ensembl_gene_id":"ENSG00000274772.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":144683169,"end":144683464,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000206724.1","gene_symbol":"RNU6-756P","gene_name":"RNA, U6 small nuclear 756, pseudogene [Source:HGNC Symbol;Acc:HGNC:47719]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479900","summary":null,"start":124260646,"end":124260752,"strand":1,"description":"RNA, U6 small nuclear 756, pseudogene [Source:HGNC Symbol;Acc:HGNC:47719]"}, {"versioned_ensembl_gene_id":"ENSG00000265373.2","gene_symbol":"MIR3180-2","gene_name":"microRNA 3180-2 [Source:HGNC Symbol;Acc:HGNC:38343]","synonyms":"hsa-mir-3180-2","biotype":"miRNA","ncbi_id":"100422956","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16309879,"end":16309966,"strand":1,"description":"microRNA 3180-2 [Source:HGNC Symbol;Acc:HGNC:38343]"}, {"versioned_ensembl_gene_id":"ENSG00000221440.1","gene_symbol":"RNU6ATAC31P","gene_name":"RNA, U6atac small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:46930]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481169","summary":null,"start":88206427,"end":88206552,"strand":-1,"description":"RNA, U6atac small nuclear 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:46930]"}, {"versioned_ensembl_gene_id":"ENSG00000275809.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":21307731,"end":21307837,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000283819.1","gene_symbol":"MIR144","gene_name":"microRNA 144 [Source:HGNC Symbol;Acc:HGNC:31531]","synonyms":"MIRN144,hsa-mir-144","biotype":"miRNA","ncbi_id":"406936","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28861533,"end":28861618,"strand":-1,"description":"microRNA 144 [Source:HGNC Symbol;Acc:HGNC:31531]"}, {"versioned_ensembl_gene_id":"ENSG00000207443.1","gene_symbol":"RNU6-417P","gene_name":"RNA, U6 small nuclear 417, pseudogene [Source:HGNC Symbol;Acc:HGNC:47380]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479750","summary":null,"start":63011463,"end":63011569,"strand":-1,"description":"RNA, U6 small nuclear 417, pseudogene [Source:HGNC Symbol;Acc:HGNC:47380]"}, {"versioned_ensembl_gene_id":"ENSG00000284399.1","gene_symbol":"MIR3184","gene_name":"microRNA 3184 [Source:HGNC Symbol;Acc:HGNC:38182]","synonyms":"hsa-mir-3184","biotype":"miRNA","ncbi_id":"100423003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30117086,"end":30117160,"strand":-1,"description":"microRNA 3184 [Source:HGNC Symbol;Acc:HGNC:38182]"}, {"versioned_ensembl_gene_id":"ENSG00000201724.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99681786,"end":99681877,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000244308.2","gene_symbol":"RN7SL762P","gene_name":"RNA, 7SL, cytoplasmic 762, pseudogene [Source:HGNC Symbol;Acc:HGNC:46778]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479500","summary":null,"start":120110498,"end":120110786,"strand":-1,"description":"RNA, 7SL, cytoplasmic 762, pseudogene [Source:HGNC Symbol;Acc:HGNC:46778]"}, {"versioned_ensembl_gene_id":"ENSG00000275775.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46660217,"end":46660318,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222784.1","gene_symbol":"RN7SKP91","gene_name":"RNA, 7SK small nuclear pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:45815]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480861","summary":null,"start":30843823,"end":30844110,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 91 [Source:HGNC Symbol;Acc:HGNC:45815]"}, {"versioned_ensembl_gene_id":"ENSG00000263602.1","gene_symbol":"MIR3185","gene_name":"microRNA 3185 [Source:HGNC Symbol;Acc:HGNC:38391]","synonyms":"hsa-mir-3185","biotype":"miRNA","ncbi_id":"100422978","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48724408,"end":48724475,"strand":-1,"description":"microRNA 3185 [Source:HGNC Symbol;Acc:HGNC:38391]"}, {"versioned_ensembl_gene_id":"ENSG00000199411.1","gene_symbol":"SNORD62","gene_name":"Small nucleolar RNA SNORD62 [Source:RFAM;Acc:RF00153]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":137094345,"end":137094430,"strand":1,"description":"Small nucleolar RNA SNORD62 [Source:RFAM;Acc:RF00153]"}, {"versioned_ensembl_gene_id":"ENSG00000201329.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":43378297,"end":43378510,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000222313.1","gene_symbol":"RN7SKP267","gene_name":"RNA, 7SK small nuclear pseudogene 267 [Source:HGNC Symbol;Acc:HGNC:45991]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480478","summary":null,"start":148822164,"end":148822448,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 267 [Source:HGNC Symbol;Acc:HGNC:45991]"}, {"versioned_ensembl_gene_id":"ENSG00000284574.1","gene_symbol":"MIR6787","gene_name":"microRNA 6787 [Source:HGNC Symbol;Acc:HGNC:50209]","synonyms":"hsa-mir-6787","biotype":"miRNA","ncbi_id":"102465472","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":82236668,"end":82236728,"strand":1,"description":"microRNA 6787 [Source:HGNC Symbol;Acc:HGNC:50209]"}, {"versioned_ensembl_gene_id":"ENSG00000283724.1","gene_symbol":"MIR6732","gene_name":"microRNA 6732 [Source:HGNC Symbol;Acc:HGNC:50066]","synonyms":"hsa-mir-6732","biotype":"miRNA","ncbi_id":"102465438","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37480230,"end":37480289,"strand":1,"description":"microRNA 6732 [Source:HGNC Symbol;Acc:HGNC:50066]"}, {"versioned_ensembl_gene_id":"ENSG00000283928.1","gene_symbol":"MIR637","gene_name":"microRNA 637 [Source:HGNC Symbol;Acc:HGNC:32893]","synonyms":"MIRN637,hsa-mir-637","biotype":"miRNA","ncbi_id":"693222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3961414,"end":3961512,"strand":-1,"description":"microRNA 637 [Source:HGNC Symbol;Acc:HGNC:32893]"}, {"versioned_ensembl_gene_id":"ENSG00000244314.3","gene_symbol":"RN7SL36P","gene_name":"RNA, 7SL, cytoplasmic 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46052]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479237","summary":null,"start":195146728,"end":195147003,"strand":-1,"description":"RNA, 7SL, cytoplasmic 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46052]"}, {"versioned_ensembl_gene_id":"ENSG00000200376.1","gene_symbol":"RNU5E-10P","gene_name":"RNA, U5E small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:42533]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873888","summary":null,"start":47576471,"end":47576588,"strand":-1,"description":"RNA, U5E small nuclear 10, pseudogene [Source:HGNC Symbol;Acc:HGNC:42533]"}, {"versioned_ensembl_gene_id":"ENSG00000222870.1","gene_symbol":"RNU6-1328P","gene_name":"RNA, U6 small nuclear 1328, pseudogene [Source:HGNC Symbol;Acc:HGNC:48291]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480146","summary":null,"start":94495299,"end":94495404,"strand":1,"description":"RNA, U6 small nuclear 1328, pseudogene [Source:HGNC Symbol;Acc:HGNC:48291]"}, {"versioned_ensembl_gene_id":"ENSG00000266262.1","gene_symbol":"MIR4428","gene_name":"microRNA 4428 [Source:HGNC Symbol;Acc:HGNC:41667]","synonyms":"hsa-mir-4428","biotype":"miRNA","ncbi_id":"100616141","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":237471119,"end":237471191,"strand":1,"description":"microRNA 4428 [Source:HGNC Symbol;Acc:HGNC:41667]"}, {"versioned_ensembl_gene_id":"ENSG00000265137.3","gene_symbol":"MIR3192","gene_name":"microRNA 3192 [Source:HGNC Symbol;Acc:HGNC:38202]","synonyms":"hsa-mir-3192","biotype":"miRNA","ncbi_id":"100422875","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18470615,"end":18470691,"strand":1,"description":"microRNA 3192 [Source:HGNC Symbol;Acc:HGNC:38202]"}, {"versioned_ensembl_gene_id":"ENSG00000200779.1","gene_symbol":"RNU6-105P","gene_name":"RNA, U6 small nuclear 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:47068]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481210","summary":null,"start":71379755,"end":71379858,"strand":-1,"description":"RNA, U6 small nuclear 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:47068]"}, {"versioned_ensembl_gene_id":"ENSG00000202054.1","gene_symbol":"RNA5SP152","gene_name":"RNA, 5S ribosomal pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:43052]","synonyms":"RN5S152","biotype":"rRNA","ncbi_id":"100873418","summary":null,"start":8393015,"end":8393124,"strand":1,"description":"RNA, 5S ribosomal pseudogene 152 [Source:HGNC Symbol;Acc:HGNC:43052]"}, {"versioned_ensembl_gene_id":"ENSG00000202569.4","gene_symbol":"MIR146B","gene_name":"microRNA 146b [Source:HGNC Symbol;Acc:HGNC:32079]","synonyms":"MIRN146B,hsa-mir-146b","biotype":"miRNA","ncbi_id":"574447","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102436512,"end":102436584,"strand":1,"description":"microRNA 146b [Source:HGNC Symbol;Acc:HGNC:32079]"}, {"versioned_ensembl_gene_id":"ENSG00000200431.1","gene_symbol":"RNU4-81P","gene_name":"RNA, U4 small nuclear 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:47017]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479595","summary":null,"start":70450879,"end":70451022,"strand":1,"description":"RNA, U4 small nuclear 81, pseudogene [Source:HGNC Symbol;Acc:HGNC:47017]"}, {"versioned_ensembl_gene_id":"ENSG00000202174.1","gene_symbol":"RNA5-8SP5","gene_name":"RNA, 5.8S ribosomal pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41959]","synonyms":"RN5-8S5","biotype":"rRNA","ncbi_id":"100873335","summary":null,"start":132253154,"end":132253305,"strand":-1,"description":"RNA, 5.8S ribosomal pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:41959]"}, {"versioned_ensembl_gene_id":"ENSG00000252283.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28061967,"end":28062068,"strand":1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000199446.1","gene_symbol":"RNU6-543P","gene_name":"RNA, U6 small nuclear 543, pseudogene [Source:HGNC Symbol;Acc:HGNC:47506]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479807","summary":null,"start":63110139,"end":63110246,"strand":1,"description":"RNA, U6 small nuclear 543, pseudogene [Source:HGNC Symbol;Acc:HGNC:47506]"}, {"versioned_ensembl_gene_id":"ENSG00000221091.1","gene_symbol":"MIR1302-5","gene_name":"microRNA 1302-5 [Source:HGNC Symbol;Acc:HGNC:35297]","synonyms":"hsa-mir-1302-5,MIRN1302-5","biotype":"miRNA","ncbi_id":"100302146","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50614636,"end":50614785,"strand":-1,"description":"microRNA 1302-5 [Source:HGNC Symbol;Acc:HGNC:35297]"}, {"versioned_ensembl_gene_id":"ENSG00000276991.1","gene_symbol":"MIAT_exon5_3","gene_name":"Myocardial infarction associated transcript exon 5 conserved region 3 [Source:RFAM;Acc:RF01877]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":26673254,"end":26673630,"strand":1,"description":"Myocardial infarction associated transcript exon 5 conserved region 3 [Source:RFAM;Acc:RF01877]"}, {"versioned_ensembl_gene_id":"ENSG00000251905.1","gene_symbol":"RNU7-2P","gene_name":"RNA, U7 small nuclear 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:34098]","synonyms":"U7.2","biotype":"snRNA","ncbi_id":"100147745","summary":null,"start":146145156,"end":146145217,"strand":1,"description":"RNA, U7 small nuclear 2 pseudogene [Source:HGNC Symbol;Acc:HGNC:34098]"}, {"versioned_ensembl_gene_id":"ENSG00000276857.1","gene_symbol":"MIR6715A","gene_name":"microRNA 6715a [Source:HGNC Symbol;Acc:HGNC:49996]","synonyms":"hsa-mir-6715a","biotype":"miRNA","ncbi_id":"102466189","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112299612,"end":112299690,"strand":1,"description":"microRNA 6715a [Source:HGNC Symbol;Acc:HGNC:49996]"}, {"versioned_ensembl_gene_id":"ENSG00000206741.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":172779982,"end":172780094,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277826.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93637179,"end":93637338,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000244003.3","gene_symbol":"RN7SL143P","gene_name":"RNA, 7SL, cytoplasmic 143, pseudogene [Source:HGNC Symbol;Acc:HGNC:46159]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479273","summary":null,"start":58770524,"end":58770820,"strand":1,"description":"RNA, 7SL, cytoplasmic 143, pseudogene [Source:HGNC Symbol;Acc:HGNC:46159]"}, {"versioned_ensembl_gene_id":"ENSG00000266463.1","gene_symbol":"MIR3196","gene_name":"microRNA 3196 [Source:HGNC Symbol;Acc:HGNC:38198]","synonyms":"hsa-mir-3196","biotype":"miRNA","ncbi_id":"100423014","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63238779,"end":63238842,"strand":1,"description":"microRNA 3196 [Source:HGNC Symbol;Acc:HGNC:38198]"}, {"versioned_ensembl_gene_id":"ENSG00000273700.1","gene_symbol":"MIR6760","gene_name":"microRNA 6760 [Source:HGNC Symbol;Acc:HGNC:49955]","synonyms":"hsa-mir-6760","biotype":"miRNA","ncbi_id":"102465455","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111304142,"end":111304209,"strand":1,"description":"microRNA 6760 [Source:HGNC Symbol;Acc:HGNC:49955]"}, {"versioned_ensembl_gene_id":"ENSG00000211137.1","gene_symbol":"MIR190A","gene_name":"microRNA 190a [Source:HGNC Symbol;Acc:HGNC:31560]","synonyms":"MIRN190,MIR190,hsa-mir-190","biotype":"miRNA","ncbi_id":"406965","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62823957,"end":62824041,"strand":1,"description":"microRNA 190a [Source:HGNC Symbol;Acc:HGNC:31560]"}, {"versioned_ensembl_gene_id":"ENSG00000252900.1","gene_symbol":"RNU6-303P","gene_name":"RNA, U6 small nuclear 303, pseudogene [Source:HGNC Symbol;Acc:HGNC:47266]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479702","summary":null,"start":4174985,"end":4175090,"strand":-1,"description":"RNA, U6 small nuclear 303, pseudogene [Source:HGNC Symbol;Acc:HGNC:47266]"}, {"versioned_ensembl_gene_id":"ENSG00000252874.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47820200,"end":47820289,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239053.1","gene_symbol":"RNU7-138P","gene_name":"RNA, U7 small nuclear 138 pseudogene [Source:HGNC Symbol;Acc:HGNC:45672]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481801","summary":null,"start":10744186,"end":10744249,"strand":1,"description":"RNA, U7 small nuclear 138 pseudogene [Source:HGNC Symbol;Acc:HGNC:45672]"}, {"versioned_ensembl_gene_id":"ENSG00000212149.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":42940575,"end":42940702,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000266299.1","gene_symbol":"MIR3118-1","gene_name":"microRNA 3118-1 [Source:HGNC Symbol;Acc:HGNC:38265]","synonyms":"hsa-mir-3118-1","biotype":"miRNA","ncbi_id":"100423008","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13644775,"end":13644850,"strand":-1,"description":"microRNA 3118-1 [Source:HGNC Symbol;Acc:HGNC:38265]"}, {"versioned_ensembl_gene_id":"ENSG00000238628.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":87720915,"end":87721018,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000201565.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":67297653,"end":67297754,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264951.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31833247,"end":31833349,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207965.1","gene_symbol":"MIR629","gene_name":"microRNA 629 [Source:HGNC Symbol;Acc:HGNC:32885]","synonyms":"MIRN629,hsa-mir-629","biotype":"miRNA","ncbi_id":"693214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":70079372,"end":70079468,"strand":-1,"description":"microRNA 629 [Source:HGNC Symbol;Acc:HGNC:32885]"}, {"versioned_ensembl_gene_id":"ENSG00000207404.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":108891437,"end":108891546,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212280.1","gene_symbol":"RNA5SP256","gene_name":"RNA, 5S ribosomal pseudogene 256 [Source:HGNC Symbol;Acc:HGNC:43156]","synonyms":"RN5S256","biotype":"rRNA","ncbi_id":"100873510","summary":null,"start":17748118,"end":17748230,"strand":1,"description":"RNA, 5S ribosomal pseudogene 256 [Source:HGNC Symbol;Acc:HGNC:43156]"}, {"versioned_ensembl_gene_id":"ENSG00000265859.1","gene_symbol":"MIR5704","gene_name":"microRNA 5704 [Source:HGNC Symbol;Acc:HGNC:43469]","synonyms":"hsa-mir-5704","biotype":"miRNA","ncbi_id":"100847040","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":131985855,"end":131985931,"strand":-1,"description":"microRNA 5704 [Source:HGNC Symbol;Acc:HGNC:43469]"}, {"versioned_ensembl_gene_id":"ENSG00000264399.1","gene_symbol":"MIR4736","gene_name":"microRNA 4736 [Source:HGNC Symbol;Acc:HGNC:41804]","synonyms":"hsa-mir-4736","biotype":"miRNA","ncbi_id":"100616220","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":58335976,"end":58336022,"strand":-1,"description":"microRNA 4736 [Source:HGNC Symbol;Acc:HGNC:41804]"}, {"versioned_ensembl_gene_id":"ENSG00000274984.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73067231,"end":73067332,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252395.2","gene_symbol":"RNU6-1007P","gene_name":"RNA, U6 small nuclear 1007, pseudogene [Source:HGNC Symbol;Acc:HGNC:47970]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480629","summary":null,"start":88414898,"end":88415004,"strand":-1,"description":"RNA, U6 small nuclear 1007, pseudogene [Source:HGNC Symbol;Acc:HGNC:47970]"}, {"versioned_ensembl_gene_id":"ENSG00000222898.1","gene_symbol":"RN7SKP97","gene_name":"RNA, 7SK small nuclear pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:45821]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480463","summary":null,"start":61631680,"end":61632012,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 97 [Source:HGNC Symbol;Acc:HGNC:45821]"}, {"versioned_ensembl_gene_id":"ENSG00000263445.1","gene_symbol":"MIR4450","gene_name":"microRNA 4450 [Source:HGNC Symbol;Acc:HGNC:41725]","synonyms":"hsa-mir-4450","biotype":"miRNA","ncbi_id":"100616299","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76573568,"end":76573632,"strand":1,"description":"microRNA 4450 [Source:HGNC Symbol;Acc:HGNC:41725]"}, {"versioned_ensembl_gene_id":"ENSG00000222640.1","gene_symbol":"RNU2-51P","gene_name":"RNA, U2 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:48544]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480415","summary":null,"start":70360892,"end":70361088,"strand":1,"description":"RNA, U2 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:48544]"}, {"versioned_ensembl_gene_id":"ENSG00000265885.2","gene_symbol":"RN7SL783P","gene_name":"RNA, 7SL, cytoplasmic 783, pseudogene [Source:HGNC Symbol;Acc:HGNC:46799]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479505","summary":null,"start":110097851,"end":110098151,"strand":-1,"description":"RNA, 7SL, cytoplasmic 783, pseudogene [Source:HGNC Symbol;Acc:HGNC:46799]"}, {"versioned_ensembl_gene_id":"ENSG00000207395.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69406441,"end":69406552,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264961.1","gene_symbol":"MIR4730","gene_name":"microRNA 4730 [Source:HGNC Symbol;Acc:HGNC:41880]","synonyms":"hsa-mir-4730","biotype":"miRNA","ncbi_id":"100616359","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80419418,"end":80419493,"strand":1,"description":"microRNA 4730 [Source:HGNC Symbol;Acc:HGNC:41880]"}, {"versioned_ensembl_gene_id":"ENSG00000207105.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48995912,"end":48996022,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276626.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":124792319,"end":124792562,"strand":-1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000222862.2","gene_symbol":"RNU6-1086P","gene_name":"RNA, U6 small nuclear 1086, pseudogene [Source:HGNC Symbol;Acc:HGNC:48049]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481934","summary":null,"start":27679836,"end":27679935,"strand":1,"description":"RNA, U6 small nuclear 1086, pseudogene [Source:HGNC Symbol;Acc:HGNC:48049]"}, {"versioned_ensembl_gene_id":"ENSG00000276961.1","gene_symbol":"MIR7848","gene_name":"microRNA 7848 [Source:HGNC Symbol;Acc:HGNC:50058]","synonyms":"hsa-mir-7848","biotype":"miRNA","ncbi_id":"102466865","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133046481,"end":133046581,"strand":-1,"description":"microRNA 7848 [Source:HGNC Symbol;Acc:HGNC:50058]"}, {"versioned_ensembl_gene_id":"ENSG00000266582.1","gene_symbol":"MIR4527","gene_name":"microRNA 4527 [Source:HGNC Symbol;Acc:HGNC:41633]","synonyms":"hsa-mir-4527","biotype":"miRNA","ncbi_id":"100616264","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47380496,"end":47380565,"strand":1,"description":"microRNA 4527 [Source:HGNC Symbol;Acc:HGNC:41633]"}, {"versioned_ensembl_gene_id":"ENSG00000202400.1","gene_symbol":"SNORD82","gene_name":"small nucleolar RNA, C/D box 82 [Source:HGNC Symbol;Acc:HGNC:10240]","synonyms":"RNU82,Z25,U82","biotype":"snoRNA","ncbi_id":"25826","summary":"The majority of small nucleolar RNAs (snoRNAs) function as guide RNAs in the nucleotide modification of preribosomal RNA (pre-rRNA). C/D box snoRNAs, like SNORD82, are involved in site-specific 2-prime-O-ribose methylation of pre-rRNA (Rebane and Metspalu, 1999 [PubMed 10524220]).[supplied by OMIM, Mar 2008]","start":231460371,"end":231460440,"strand":-1,"description":"small nucleolar RNA, C/D box 82 [Source:HGNC Symbol;Acc:HGNC:10240]"}, {"versioned_ensembl_gene_id":"ENSG00000222664.1","gene_symbol":"RN7SKP123","gene_name":"RNA, 7SK small nuclear pseudogene 123 [Source:HGNC Symbol;Acc:HGNC:45847]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479149","summary":null,"start":93026252,"end":93026542,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 123 [Source:HGNC Symbol;Acc:HGNC:45847]"}, {"versioned_ensembl_gene_id":"ENSG00000274430.1","gene_symbol":"JPX_1","gene_name":"JPX transcript, XIST activator conserved region 1 [Source:RFAM;Acc:RF02124]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73944332,"end":73944466,"strand":1,"description":"JPX transcript, XIST activator conserved region 1 [Source:RFAM;Acc:RF02124]"}, {"versioned_ensembl_gene_id":"ENSG00000264158.1","gene_symbol":"MIR4670","gene_name":"microRNA 4670 [Source:HGNC Symbol;Acc:HGNC:41862]","synonyms":"hsa-mir-4670","biotype":"miRNA","ncbi_id":"100616351","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":92527984,"end":92528058,"strand":-1,"description":"microRNA 4670 [Source:HGNC Symbol;Acc:HGNC:41862]"}, {"versioned_ensembl_gene_id":"ENSG00000263354.1","gene_symbol":"MIR5011","gene_name":"microRNA 5011 [Source:HGNC Symbol;Acc:HGNC:43496]","synonyms":"hsa-mir-5011","biotype":"miRNA","ncbi_id":"100847002","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67081584,"end":67081686,"strand":1,"description":"microRNA 5011 [Source:HGNC Symbol;Acc:HGNC:43496]"}, {"versioned_ensembl_gene_id":"ENSG00000201364.1","gene_symbol":"RN7SKP37","gene_name":"RNA, 7SK small nuclear pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45761]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480844","summary":null,"start":21933143,"end":21933438,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:45761]"}, {"versioned_ensembl_gene_id":"ENSG00000222054.1","gene_symbol":"RNA5SP177","gene_name":"RNA, 5S ribosomal pseudogene 177 [Source:HGNC Symbol;Acc:HGNC:43077]","synonyms":"RN5S177","biotype":"rRNA","ncbi_id":"100873439","summary":null,"start":9760907,"end":9761013,"strand":1,"description":"RNA, 5S ribosomal pseudogene 177 [Source:HGNC Symbol;Acc:HGNC:43077]"}, {"versioned_ensembl_gene_id":"ENSG00000207722.1","gene_symbol":"MIR520B","gene_name":"microRNA 520b [Source:HGNC Symbol;Acc:HGNC:32105]","synonyms":"MIRN520B,hsa-mir-520b","biotype":"miRNA","ncbi_id":"574473","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53701227,"end":53701287,"strand":1,"description":"microRNA 520b [Source:HGNC Symbol;Acc:HGNC:32105]"}, {"versioned_ensembl_gene_id":"ENSG00000207758.1","gene_symbol":"MIR532","gene_name":"microRNA 532 [Source:HGNC Symbol;Acc:HGNC:32795]","synonyms":"MIRN532,hsa-mir-532","biotype":"miRNA","ncbi_id":"693124","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50003148,"end":50003238,"strand":1,"description":"microRNA 532 [Source:HGNC Symbol;Acc:HGNC:32795]"}, {"versioned_ensembl_gene_id":"ENSG00000283569.1","gene_symbol":"MIR4773-1","gene_name":"microRNA 4773-1 [Source:HGNC Symbol;Acc:HGNC:41699]","synonyms":"hsa-mir-4773-1","biotype":"miRNA","ncbi_id":"100616392","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":151368334,"end":151368411,"strand":-1,"description":"microRNA 4773-1 [Source:HGNC Symbol;Acc:HGNC:41699]"}, {"versioned_ensembl_gene_id":"ENSG00000275586.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":148876018,"end":148876286,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000274647.1","gene_symbol":"DLEU2_6","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 6 [Source:RFAM;Acc:RF02110]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":91632912,"end":91633023,"strand":-1,"description":"Deleted in lymphocytic leukemia 2 conserved region 6 [Source:RFAM;Acc:RF02110]"}, {"versioned_ensembl_gene_id":"ENSG00000212354.1","gene_symbol":"RNU6-1242P","gene_name":"RNA, U6 small nuclear 1242, pseudogene [Source:HGNC Symbol;Acc:HGNC:48205]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480108","summary":null,"start":39678520,"end":39678622,"strand":-1,"description":"RNA, U6 small nuclear 1242, pseudogene [Source:HGNC Symbol;Acc:HGNC:48205]"}, {"versioned_ensembl_gene_id":"ENSG00000252957.1","gene_symbol":"RNA5SP402","gene_name":"RNA, 5S ribosomal pseudogene 402 [Source:HGNC Symbol;Acc:HGNC:43302]","synonyms":"RN5S402","biotype":"rRNA","ncbi_id":"100873655","summary":null,"start":100074081,"end":100074190,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 402 [Source:HGNC Symbol;Acc:HGNC:43302]"}, {"versioned_ensembl_gene_id":"ENSG00000199030.2","gene_symbol":"MIRLET7C","gene_name":"microRNA let-7c [Source:HGNC Symbol;Acc:HGNC:31480]","synonyms":"MIRNLET7C,hsa-let-7c","biotype":"miRNA","ncbi_id":"406885","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16539828,"end":16539911,"strand":1,"description":"microRNA let-7c [Source:HGNC Symbol;Acc:HGNC:31480]"}, {"versioned_ensembl_gene_id":"ENSG00000200390.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127829747,"end":127829852,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207401.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":110934406,"end":110934507,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207780.1","gene_symbol":"MIR648","gene_name":"microRNA 648 [Source:HGNC Symbol;Acc:HGNC:32904]","synonyms":"MIRN648,hsa-mir-648","biotype":"miRNA","ncbi_id":"693233","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17980868,"end":17980961,"strand":-1,"description":"microRNA 648 [Source:HGNC Symbol;Acc:HGNC:32904]"}, {"versioned_ensembl_gene_id":"ENSG00000275615.1","gene_symbol":"RNU6-1207P","gene_name":"RNA, U6 small nuclear 1207, pseudogene [Source:HGNC Symbol;Acc:HGNC:48170]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480648","summary":null,"start":45188790,"end":45188896,"strand":-1,"description":"RNA, U6 small nuclear 1207, pseudogene [Source:HGNC Symbol;Acc:HGNC:48170]"}, {"versioned_ensembl_gene_id":"ENSG00000252315.1","gene_symbol":"RNA5SP520","gene_name":"RNA, 5S ribosomal pseudogene 520 [Source:HGNC Symbol;Acc:HGNC:43420]","synonyms":"RN5S520","biotype":"rRNA","ncbi_id":"106480771","summary":null,"start":17557864,"end":17557976,"strand":1,"description":"RNA, 5S ribosomal pseudogene 520 [Source:HGNC Symbol;Acc:HGNC:43420]"}, {"versioned_ensembl_gene_id":"ENSG00000207024.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64296037,"end":64296138,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277341.1","gene_symbol":"RNU6-489P","gene_name":"RNA, U6 small nuclear 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:47452]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481334","summary":null,"start":37907957,"end":37908063,"strand":1,"description":"RNA, U6 small nuclear 489, pseudogene [Source:HGNC Symbol;Acc:HGNC:47452]"}, {"versioned_ensembl_gene_id":"ENSG00000207926.1","gene_symbol":"MIR135A1","gene_name":"microRNA 135a-1 [Source:HGNC Symbol;Acc:HGNC:31520]","synonyms":"MIRN135A1,MIRN135-1,hsa-mir-135a-1,hsa-mir-135-1","biotype":"miRNA","ncbi_id":"406925","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52294219,"end":52294308,"strand":-1,"description":"microRNA 135a-1 [Source:HGNC Symbol;Acc:HGNC:31520]"}, {"versioned_ensembl_gene_id":"ENSG00000266784.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31363816,"end":31363922,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000265816.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":32026965,"end":32027085,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000202222.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39881566,"end":39881678,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200334.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":149940030,"end":149940131,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207927.1","gene_symbol":"MIR302A","gene_name":"microRNA 302a [Source:HGNC Symbol;Acc:HGNC:31623]","synonyms":"MIRN302A,MIRN302,hsa-mir-302a,hsa-mir-302","biotype":"miRNA","ncbi_id":"407028","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112648183,"end":112648251,"strand":-1,"description":"microRNA 302a [Source:HGNC Symbol;Acc:HGNC:31623]"}, {"versioned_ensembl_gene_id":"ENSG00000263947.2","gene_symbol":"RN7SL274P","gene_name":"RNA, 7SL, cytoplasmic 274, pseudogene [Source:HGNC Symbol;Acc:HGNC:46290]","synonyms":"RN7SL694P","biotype":"misc_RNA","ncbi_id":"106479322","summary":null,"start":14601823,"end":14602094,"strand":-1,"description":"RNA, 7SL, cytoplasmic 274, pseudogene [Source:HGNC Symbol;Acc:HGNC:46290]"}, {"versioned_ensembl_gene_id":"ENSG00000199035.2","gene_symbol":"MIR103A1","gene_name":"microRNA 103a-1 [Source:HGNC Symbol;Acc:HGNC:31490]","synonyms":"MIRN103-1,MIR103-1,hsa-mir-103a-1,hsa-mir-103-1","biotype":"miRNA","ncbi_id":"406895","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":168560896,"end":168560973,"strand":-1,"description":"microRNA 103a-1 [Source:HGNC Symbol;Acc:HGNC:31490]"}, {"versioned_ensembl_gene_id":"ENSG00000199080.1","gene_symbol":"MIR133B","gene_name":"microRNA 133b [Source:HGNC Symbol;Acc:HGNC:31759]","synonyms":"MIRN133B,hsa-mir-133b","biotype":"miRNA","ncbi_id":"442890","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The encoded miRNA is considered a canonical myomiR and is important for normal cardiac and skeletal muscle development. It is additionally important for normal development in non-muscle tissues, and is abnormally expressed in a variety of cancers. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2017]","start":52148923,"end":52149041,"strand":1,"description":"microRNA 133b [Source:HGNC Symbol;Acc:HGNC:31759]"}, {"versioned_ensembl_gene_id":"ENSG00000252352.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":69355133,"end":69355218,"strand":-1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000206929.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101446825,"end":101446932,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212556.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":127202372,"end":127202473,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275504.1","gene_symbol":"U7","gene_name":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":68926894,"end":68926957,"strand":-1,"description":"U7 small nuclear RNA [Source:RFAM;Acc:RF00066]"}, {"versioned_ensembl_gene_id":"ENSG00000263514.1","gene_symbol":"MIR3668","gene_name":"microRNA 3668 [Source:HGNC Symbol;Acc:HGNC:38982]","synonyms":"hsa-mir-3668","biotype":"miRNA","ncbi_id":"100500879","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140205252,"end":140205326,"strand":1,"description":"microRNA 3668 [Source:HGNC Symbol;Acc:HGNC:38982]"}, {"versioned_ensembl_gene_id":"ENSG00000207960.1","gene_symbol":"MIR153-2","gene_name":"microRNA 153-2 [Source:HGNC Symbol;Acc:HGNC:31540]","synonyms":"MIRN153-2,hsa-mir-153-2","biotype":"miRNA","ncbi_id":"406945","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":157574336,"end":157574422,"strand":-1,"description":"microRNA 153-2 [Source:HGNC Symbol;Acc:HGNC:31540]"}, {"versioned_ensembl_gene_id":"ENSG00000238344.1","gene_symbol":"SNORD126","gene_name":"small nucleolar RNA, C/D box 126 [Source:HGNC Symbol;Acc:HGNC:33565]","synonyms":"MIRN1201,MIR1201,hsa-mir-1201","biotype":"snoRNA","ncbi_id":"100113391","summary":null,"start":20326450,"end":20326526,"strand":-1,"description":"small nucleolar RNA, C/D box 126 [Source:HGNC Symbol;Acc:HGNC:33565]"}, {"versioned_ensembl_gene_id":"ENSG00000284321.1","gene_symbol":"MIR124-1","gene_name":"microRNA 124-1 [Source:HGNC Symbol;Acc:HGNC:31502]","synonyms":"MIRN124-1,hsa-mir-124a-1,hsa-mir-124-1,MIRN124A1","biotype":"miRNA","ncbi_id":"406907","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9903388,"end":9903472,"strand":-1,"description":"microRNA 124-1 [Source:HGNC Symbol;Acc:HGNC:31502]"}, {"versioned_ensembl_gene_id":"ENSG00000199572.1","gene_symbol":"RNA5SP174","gene_name":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]","synonyms":"RN5S174","biotype":"rRNA","ncbi_id":"106478998","summary":null,"start":190015138,"end":190015255,"strand":1,"description":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]"}, {"versioned_ensembl_gene_id":"ENSG00000277762.1","gene_symbol":"RN7SL261P","gene_name":"RNA, 7SL, cytoplasmic 261, pseudogene [Source:HGNC Symbol;Acc:HGNC:46277]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479316","summary":null,"start":147689256,"end":147689537,"strand":1,"description":"RNA, 7SL, cytoplasmic 261, pseudogene [Source:HGNC Symbol;Acc:HGNC:46277]"}, {"versioned_ensembl_gene_id":"ENSG00000284062.1","gene_symbol":"MIR4469","gene_name":"microRNA 4469 [Source:HGNC Symbol;Acc:HGNC:41556]","synonyms":"hsa-mir-4469","biotype":"miRNA","ncbi_id":"100616115","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42896197,"end":42896275,"strand":-1,"description":"microRNA 4469 [Source:HGNC Symbol;Acc:HGNC:41556]"}, {"versioned_ensembl_gene_id":"ENSG00000200681.1","gene_symbol":"RNU6-263P","gene_name":"RNA, U6 small nuclear 263, pseudogene [Source:HGNC Symbol;Acc:HGNC:47226]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479683","summary":null,"start":18306973,"end":18307079,"strand":-1,"description":"RNA, U6 small nuclear 263, pseudogene [Source:HGNC Symbol;Acc:HGNC:47226]"}, {"versioned_ensembl_gene_id":"ENSG00000277836.1","gene_symbol":"AC141272.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1270984,"end":1271271,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000202268.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":45255409,"end":45255620,"strand":-1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000200483.1","gene_symbol":"RNU6-1017P","gene_name":"RNA, U6 small nuclear 1017, pseudogene [Source:HGNC Symbol;Acc:HGNC:47980]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480014","summary":null,"start":131815263,"end":131815368,"strand":-1,"description":"RNA, U6 small nuclear 1017, pseudogene [Source:HGNC Symbol;Acc:HGNC:47980]"}, {"versioned_ensembl_gene_id":"ENSG00000265112.1","gene_symbol":"MIR3153","gene_name":"microRNA 3153 [Source:HGNC Symbol;Acc:HGNC:38289]","synonyms":"hsa-mir-3153","biotype":"miRNA","ncbi_id":"100422936","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":89312225,"end":89312306,"strand":1,"description":"microRNA 3153 [Source:HGNC Symbol;Acc:HGNC:38289]"}, {"versioned_ensembl_gene_id":"ENSG00000207563.1","gene_symbol":"MIR23B","gene_name":"microRNA 23b [Source:HGNC Symbol;Acc:HGNC:31606]","synonyms":"MIRN23B,hsa-mir-23b","biotype":"miRNA","ncbi_id":"407011","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95085208,"end":95085304,"strand":1,"description":"microRNA 23b [Source:HGNC Symbol;Acc:HGNC:31606]"}, {"versioned_ensembl_gene_id":"ENSG00000275559.1","gene_symbol":"DLEU2_6","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 6 [Source:RFAM;Acc:RF02110]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50081843,"end":50081978,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 6 [Source:RFAM;Acc:RF02110]"}, {"versioned_ensembl_gene_id":"ENSG00000207223.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64652888,"end":64652989,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276124.1","gene_symbol":"MIR6855","gene_name":"microRNA 6855 [Source:HGNC Symbol;Acc:HGNC:50061]","synonyms":"hsa-mir-6855","biotype":"miRNA","ncbi_id":"102466750","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129869605,"end":129869671,"strand":1,"description":"microRNA 6855 [Source:HGNC Symbol;Acc:HGNC:50061]"}, {"versioned_ensembl_gene_id":"ENSG00000207453.1","gene_symbol":"RNU6-535P","gene_name":"RNA, U6 small nuclear 535, pseudogene [Source:HGNC Symbol;Acc:HGNC:47498]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479803","summary":null,"start":7486703,"end":7486809,"strand":-1,"description":"RNA, U6 small nuclear 535, pseudogene [Source:HGNC Symbol;Acc:HGNC:47498]"}, {"versioned_ensembl_gene_id":"ENSG00000201260.1","gene_symbol":"RNU6-1075P","gene_name":"RNA, U6 small nuclear 1075, pseudogene [Source:HGNC Symbol;Acc:HGNC:48038]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480406","summary":null,"start":16207821,"end":16207927,"strand":-1,"description":"RNA, U6 small nuclear 1075, pseudogene [Source:HGNC Symbol;Acc:HGNC:48038]"}, {"versioned_ensembl_gene_id":"ENSG00000222986.1","gene_symbol":"RNU5A-5P","gene_name":"RNA, U5A small nuclear 5, 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{"versioned_ensembl_gene_id":"ENSG00000276185.1","gene_symbol":"TP53TG1_2","gene_name":"TP53 target 1 conserved region 2 [Source:RFAM;Acc:RF02196]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87345305,"end":87345486,"strand":1,"description":"TP53 target 1 conserved region 2 [Source:RFAM;Acc:RF02196]"}, {"versioned_ensembl_gene_id":"ENSG00000252643.1","gene_symbol":"RNU6-1136P","gene_name":"RNA, U6 small nuclear 1136, pseudogene [Source:HGNC Symbol;Acc:HGNC:48099]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480066","summary":null,"start":102834605,"end":102834708,"strand":1,"description":"RNA, U6 small nuclear 1136, pseudogene [Source:HGNC Symbol;Acc:HGNC:48099]"}, {"versioned_ensembl_gene_id":"ENSG00000251957.1","gene_symbol":"RNU6-1095P","gene_name":"RNA, U6 small nuclear 1095, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000207394.1","gene_symbol":"RNU6-1060P","gene_name":"RNA, U6 small nuclear 1060, pseudogene [Source:HGNC Symbol;Acc:HGNC:48023]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480032","summary":null,"start":23124981,"end":23125087,"strand":-1,"description":"RNA, U6 small nuclear 1060, pseudogene [Source:HGNC Symbol;Acc:HGNC:48023]"}, {"versioned_ensembl_gene_id":"ENSG00000278817.1","gene_symbol":"AC007325.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":131494,"end":137392,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000275230.1","gene_symbol":"RN7SL544P","gene_name":"RNA, 7SL, cytoplasmic 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:46560]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481070","summary":null,"start":62363581,"end":62363864,"strand":1,"description":"RNA, 7SL, cytoplasmic 544, pseudogene [Source:HGNC Symbol;Acc:HGNC:46560]"}, {"versioned_ensembl_gene_id":"ENSG00000223229.1","gene_symbol":"RN7SKP270","gene_name":"RNA, 7SK small nuclear pseudogene 270 [Source:HGNC Symbol;Acc:HGNC:45994]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479216","summary":null,"start":96695856,"end":96696167,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 270 [Source:HGNC Symbol;Acc:HGNC:45994]"}, {"versioned_ensembl_gene_id":"ENSG00000207340.1","gene_symbol":"RNVU1-1","gene_name":"RNA, variant U1 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10133]","synonyms":"vU1.10,vU1.1,U1P14,U1.4,RNVU1-10,RNU1P10,RNU1-53,RNU1-10P","biotype":"snRNA","ncbi_id":"101954273","summary":null,"start":148362370,"end":148362533,"strand":-1,"description":"RNA, variant U1 small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10133]"}, {"versioned_ensembl_gene_id":"ENSG00000253066.1","gene_symbol":"RNU6-709P","gene_name":"RNA, U6 small nuclear 709, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252207.1","gene_symbol":"RNA5SP365","gene_name":"RNA, 5S ribosomal pseudogene 365 [Source:HGNC Symbol;Acc:HGNC:43265]","synonyms":"RN5S365","biotype":"rRNA","ncbi_id":"100873624","summary":null,"start":89726936,"end":89727042,"strand":1,"description":"RNA, 5S ribosomal pseudogene 365 [Source:HGNC Symbol;Acc:HGNC:43265]"}, {"versioned_ensembl_gene_id":"ENSG00000251920.1","gene_symbol":"RNA5SP216","gene_name":"RNA, 5S ribosomal pseudogene 216 [Source:HGNC Symbol;Acc:HGNC:43116]","synonyms":"RN5S216","biotype":"rRNA","ncbi_id":"100873476","summary":null,"start":125979812,"end":125979934,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 216 [Source:HGNC Symbol;Acc:HGNC:43116]"}, {"versioned_ensembl_gene_id":"ENSG00000200889.1","gene_symbol":"RNU4-13P","gene_name":"RNA, U4 small nuclear 13, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000274424.1","gene_symbol":"RN7SL196P","gene_name":"RNA, 7SL, cytoplasmic 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:46212]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479293","summary":null,"start":30405307,"end":30405597,"strand":-1,"description":"RNA, 7SL, cytoplasmic 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:46212]"}, {"versioned_ensembl_gene_id":"ENSG00000275853.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55731100,"end":55731403,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207173.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58083068,"end":58083168,"strand":-1,"description":"Y RNA 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{"versioned_ensembl_gene_id":"ENSG00000202392.1","gene_symbol":"RN7SKP292","gene_name":"RNA, 7SK small nuclear pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:46016]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479225","summary":null,"start":6997012,"end":6997328,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 292 [Source:HGNC Symbol;Acc:HGNC:46016]"}, {"versioned_ensembl_gene_id":"ENSG00000278696.1","gene_symbol":"RN7SL82P","gene_name":"RNA, 7SL, cytoplasmic 82, pseudogene [Source:HGNC Symbol;Acc:HGNC:46098]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480944","summary":null,"start":30800160,"end":30800396,"strand":1,"description":"RNA, 7SL, cytoplasmic 82, pseudogene [Source:HGNC Symbol;Acc:HGNC:46098]"}, {"versioned_ensembl_gene_id":"ENSG00000280894.1","gene_symbol":"SNORA50D","gene_name":"small nucleolar RNA, H/ACA box 50D [Source:HGNC 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nuclear pseudogene 77 [Source:HGNC Symbol;Acc:HGNC:45801]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479128","summary":null,"start":106679977,"end":106680329,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 77 [Source:HGNC Symbol;Acc:HGNC:45801]"}, {"versioned_ensembl_gene_id":"ENSG00000212459.1","gene_symbol":"RNU6-695P","gene_name":"RNA, U6 small nuclear 695, pseudogene [Source:HGNC Symbol;Acc:HGNC:47658]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481400","summary":null,"start":90253456,"end":90253559,"strand":-1,"description":"RNA, U6 small nuclear 695, pseudogene [Source:HGNC Symbol;Acc:HGNC:47658]"}, {"versioned_ensembl_gene_id":"ENSG00000278702.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35399997,"end":35400319,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200873.1","gene_symbol":"RNA5SP399","gene_name":"RNA, 5S ribosomal pseudogene 399 [Source:HGNC Symbol;Acc:HGNC:43299]","synonyms":"RN5S399","biotype":"rRNA","ncbi_id":"100873652","summary":null,"start":71858570,"end":71858686,"strand":1,"description":"RNA, 5S ribosomal pseudogene 399 [Source:HGNC Symbol;Acc:HGNC:43299]"}, {"versioned_ensembl_gene_id":"ENSG00000252246.1","gene_symbol":"RNA5SP92","gene_name":"RNA, 5S ribosomal pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:42890]","synonyms":"RN5S92","biotype":"rRNA","ncbi_id":"100873325","summary":null,"start":33332898,"end":33333007,"strand":1,"description":"RNA, 5S ribosomal pseudogene 92 [Source:HGNC Symbol;Acc:HGNC:42890]"}, {"versioned_ensembl_gene_id":"ENSG00000238364.1","gene_symbol":"RNU7-140P","gene_name":"RNA, U7 small nuclear 140 pseudogene [Source:HGNC Symbol;Acc:HGNC:45674]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479077","summary":null,"start":10551033,"end":10551092,"strand":-1,"description":"RNA, U7 small nuclear 140 pseudogene [Source:HGNC Symbol;Acc:HGNC:45674]"}, {"versioned_ensembl_gene_id":"ENSG00000243075.3","gene_symbol":"RN7SL519P","gene_name":"RNA, 7SL, cytoplasmic 519, pseudogene [Source:HGNC Symbol;Acc:HGNC:46535]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479412","summary":null,"start":50841498,"end":50841785,"strand":-1,"description":"RNA, 7SL, cytoplasmic 519, pseudogene [Source:HGNC Symbol;Acc:HGNC:46535]"}, {"versioned_ensembl_gene_id":"ENSG00000207215.2","gene_symbol":"SNORD3H","gene_name":"small nucleolar RNA, C/D box 3H [Source:HGNC Symbol;Acc:HGNC:52241]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617016","summary":null,"start":97358265,"end":97358478,"strand":1,"description":"small nucleolar RNA, C/D box 3H [Source:HGNC Symbol;Acc:HGNC:52241]"}, {"versioned_ensembl_gene_id":"ENSG00000277473.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11644067,"end":11644343,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283795.1","gene_symbol":"MIR4426","gene_name":"microRNA 4426 [Source:HGNC Symbol;Acc:HGNC:41848]","synonyms":"hsa-mir-4426","biotype":"miRNA","ncbi_id":"100616345","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":192716328,"end":192716390,"strand":1,"description":"microRNA 4426 [Source:HGNC Symbol;Acc:HGNC:41848]"}, {"versioned_ensembl_gene_id":"ENSG00000222414.1","gene_symbol":"RNU2-59P","gene_name":"RNA, U2 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:48552]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480223","summary":null,"start":101364845,"end":101365035,"strand":-1,"description":"RNA, U2 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:48552]"}, {"versioned_ensembl_gene_id":"ENSG00000252729.1","gene_symbol":"RNU6-971P","gene_name":"RNA, U6 small nuclear 971, pseudogene [Source:HGNC Symbol;Acc:HGNC:47934]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481926","summary":null,"start":43473585,"end":43473690,"strand":1,"description":"RNA, U6 small nuclear 971, pseudogene [Source:HGNC Symbol;Acc:HGNC:47934]"}, {"versioned_ensembl_gene_id":"ENSG00000251698.1","gene_symbol":"RNA5SP445","gene_name":"RNA, 5S ribosomal pseudogene 445 [Source:HGNC Symbol;Acc:HGNC:43345]","synonyms":"RN5S445","biotype":"rRNA","ncbi_id":"100873691","summary":null,"start":66639269,"end":66639383,"strand":1,"description":"RNA, 5S ribosomal pseudogene 445 [Source:HGNC Symbol;Acc:HGNC:43345]"}, {"versioned_ensembl_gene_id":"ENSG00000242216.3","gene_symbol":"RN7SL97P","gene_name":"RNA, 7SL, cytoplasmic 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:46113]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479258","summary":null,"start":25818234,"end":25818532,"strand":-1,"description":"RNA, 7SL, cytoplasmic 97, pseudogene [Source:HGNC Symbol;Acc:HGNC:46113]"}, {"versioned_ensembl_gene_id":"ENSG00000201608.1","gene_symbol":"RNU4-42P","gene_name":"RNA, U4 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46978]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479577","summary":null,"start":160392768,"end":160392909,"strand":-1,"description":"RNA, U4 small nuclear 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46978]"}, {"versioned_ensembl_gene_id":"ENSG00000266870.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":28916503,"end":28916602,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000275373.1","gene_symbol":"MIR6124","gene_name":"microRNA 6124 [Source:HGNC Symbol;Acc:HGNC:50200]","synonyms":"hsa-mir-6124","biotype":"miRNA","ncbi_id":"102466906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12163683,"end":12163767,"strand":1,"description":"microRNA 6124 [Source:HGNC Symbol;Acc:HGNC:50200]"}, {"versioned_ensembl_gene_id":"ENSG00000201412.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":92710499,"end":92710608,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201076.1","gene_symbol":"RNU4-51P","gene_name":"RNA, U4 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46987]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479581","summary":null,"start":60911303,"end":60911442,"strand":1,"description":"RNA, U4 small nuclear 51, pseudogene [Source:HGNC Symbol;Acc:HGNC:46987]"}, {"versioned_ensembl_gene_id":"ENSG00000266192.3","gene_symbol":"MIR1260B","gene_name":"microRNA 1260b [Source:HGNC Symbol;Acc:HGNC:38258]","synonyms":"hsa-mir-1260b","biotype":"miRNA","ncbi_id":"100422991","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96341438,"end":96341526,"strand":1,"description":"microRNA 1260b [Source:HGNC Symbol;Acc:HGNC:38258]"}, {"versioned_ensembl_gene_id":"ENSG00000263885.1","gene_symbol":"MIR3920","gene_name":"microRNA 3920 [Source:HGNC Symbol;Acc:HGNC:38974]","synonyms":"hsa-mir-3920","biotype":"miRNA","ncbi_id":"100500823","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101519820,"end":101519905,"strand":-1,"description":"microRNA 3920 [Source:HGNC Symbol;Acc:HGNC:38974]"}, {"versioned_ensembl_gene_id":"ENSG00000240641.3","gene_symbol":"RN7SL580P","gene_name":"RNA, 7SL, cytoplasmic 580, pseudogene [Source:HGNC Symbol;Acc:HGNC:46596]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481081","summary":null,"start":51975673,"end":51975959,"strand":1,"description":"RNA, 7SL, cytoplasmic 580, pseudogene [Source:HGNC Symbol;Acc:HGNC:46596]"}, {"versioned_ensembl_gene_id":"ENSG00000199883.1","gene_symbol":"RN7SKP90","gene_name":"RNA, 7SK small nuclear pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:45814]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481809","summary":null,"start":16842253,"end":16842587,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 90 [Source:HGNC Symbol;Acc:HGNC:45814]"}, {"versioned_ensembl_gene_id":"ENSG00000277642.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868977,"end":54869083,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000265861.1","gene_symbol":"MIR4495","gene_name":"microRNA 4495 [Source:HGNC Symbol;Acc:HGNC:41693]","synonyms":"hsa-mir-4495","biotype":"miRNA","ncbi_id":"100616287","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97939056,"end":97939121,"strand":-1,"description":"microRNA 4495 [Source:HGNC Symbol;Acc:HGNC:41693]"}, {"versioned_ensembl_gene_id":"ENSG00000252320.1","gene_symbol":"RNU6-320P","gene_name":"RNA, U6 small nuclear 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:47283]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480570","summary":null,"start":136583240,"end":136583345,"strand":1,"description":"RNA, U6 small nuclear 320, pseudogene [Source:HGNC Symbol;Acc:HGNC:47283]"}, {"versioned_ensembl_gene_id":"ENSG00000276319.1","gene_symbol":"MIR8079","gene_name":"microRNA 8079 [Source:HGNC Symbol;Acc:HGNC:50021]","synonyms":"hsa-mir-8079","biotype":"miRNA","ncbi_id":"102465876","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44196129,"end":44196200,"strand":-1,"description":"microRNA 8079 [Source:HGNC Symbol;Acc:HGNC:50021]"}, {"versioned_ensembl_gene_id":"ENSG00000212493.1","gene_symbol":"SNORD19","gene_name":"small nucleolar RNA, C/D box 19 [Source:HGNC Symbol;Acc:HGNC:32717]","synonyms":"HBII-108","biotype":"snoRNA","ncbi_id":"692089","summary":null,"start":52689248,"end":52689315,"strand":1,"description":"small nucleolar RNA, C/D box 19 [Source:HGNC Symbol;Acc:HGNC:32717]"}, {"versioned_ensembl_gene_id":"ENSG00000274450.1","gene_symbol":"U6atac","gene_name":"U6atac minor spliceosomal RNA [Source:RFAM;Acc:RF00619]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":146862729,"end":146862845,"strand":-1,"description":"U6atac minor spliceosomal RNA [Source:RFAM;Acc:RF00619]"}, {"versioned_ensembl_gene_id":"ENSG00000200211.1","gene_symbol":"RNY4P27","gene_name":"RNA, Ro-associated Y4 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42495]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873821","summary":null,"start":95336106,"end":95336201,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 27 [Source:HGNC Symbol;Acc:HGNC:42495]"}, {"versioned_ensembl_gene_id":"ENSG00000283856.1","gene_symbol":"MIR7703","gene_name":"microRNA 7703 [Source:HGNC Symbol;Acc:HGNC:50271]","synonyms":"hsa-mir-7703","biotype":"miRNA","ncbi_id":"102465801","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24143489,"end":24143565,"strand":-1,"description":"microRNA 7703 [Source:HGNC Symbol;Acc:HGNC:50271]"}, {"versioned_ensembl_gene_id":"ENSG00000223309.1","gene_symbol":"RNU6-722P","gene_name":"RNA, U6 small nuclear 722, pseudogene [Source:HGNC Symbol;Acc:HGNC:47685]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481407","summary":null,"start":48959179,"end":48959282,"strand":-1,"description":"RNA, U6 small nuclear 722, pseudogene [Source:HGNC Symbol;Acc:HGNC:47685]"}, {"versioned_ensembl_gene_id":"ENSG00000199508.1","gene_symbol":"RNA5SP110","gene_name":"RNA, 5S ribosomal pseudogene 110 [Source:HGNC Symbol;Acc:HGNC:42908]","synonyms":"RN5S110","biotype":"rRNA","ncbi_id":"100873380","summary":null,"start":164858432,"end":164858546,"strand":1,"description":"RNA, 5S ribosomal pseudogene 110 [Source:HGNC Symbol;Acc:HGNC:42908]"}, {"versioned_ensembl_gene_id":"ENSG00000275082.4","gene_symbol":"NLRP2","gene_name":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]","synonyms":"PAN1,FLJ20510,PAN1,NALP2,PYPAF2,CLR19.9,NALP2,PYPAF2,NBS1,CLR19.9,NBS1,FLJ20510","biotype":"protein_coding","ncbi_id":"55655","summary":"This gene is a member of the nucleotide-binding and leucine-rich repeat receptor (NLR) family, and is predicted to contain an N-terminal pyrin effector domain (PYD), a centrally-located nucleotide-binding and oligomerization domain (NACHT) and C-terminal leucine-rich repeats (LRR). Members of this gene family are thought to be important regulators of immune responses. This gene product interacts with components of the IkB kinase (IKK) complex, and can regulate both caspase-1 and NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) activity. The pyrin domain is necessary and sufficient for suppression of NF-kB activity. An allelic variant (rs147585490) has been found that is incapable of blocking the transcriptional activity of NF-kB. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]","start":54894315,"end":54930171,"strand":1,"description":"NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]"}, {"versioned_ensembl_gene_id":"ENSG00000266449.1","gene_symbol":"MIR3713","gene_name":"microRNA 3713 [Source:HGNC Symbol;Acc:HGNC:38926]","synonyms":"hsa-mir-3713","biotype":"miRNA","ncbi_id":"100500855","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76586647,"end":76586691,"strand":1,"description":"microRNA 3713 [Source:HGNC Symbol;Acc:HGNC:38926]"}, {"versioned_ensembl_gene_id":"ENSG00000277721.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46553522,"end":46553775,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000206859.1","gene_symbol":"RNU6-767P","gene_name":"RNA, U6 small nuclear 767, pseudogene [Source:HGNC Symbol;Acc:HGNC:47730]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481916","summary":null,"start":17170083,"end":17170189,"strand":1,"description":"RNA, U6 small nuclear 767, pseudogene [Source:HGNC Symbol;Acc:HGNC:47730]"}, {"versioned_ensembl_gene_id":"ENSG00000274805.1","gene_symbol":"MIR6768","gene_name":"microRNA 6768 [Source:HGNC Symbol;Acc:HGNC:50264]","synonyms":"hsa-mir-6768","biotype":"miRNA","ncbi_id":"102465460","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2463967,"end":2464038,"strand":1,"description":"microRNA 6768 [Source:HGNC Symbol;Acc:HGNC:50264]"}, {"versioned_ensembl_gene_id":"ENSG00000257381.3","gene_symbol":"MIR3179-2","gene_name":"microRNA 3179-2 [Source:HGNC Symbol;Acc:HGNC:38325]","synonyms":"hsa-mir-3179-2","biotype":"miRNA","ncbi_id":"100422886","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16300159,"end":16300242,"strand":1,"description":"microRNA 3179-2 [Source:HGNC Symbol;Acc:HGNC:38325]"}, {"versioned_ensembl_gene_id":"ENSG00000206699.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99527826,"end":99527927,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252482.1","gene_symbol":"RNU7-22P","gene_name":"RNA, U7 small nuclear 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:34118]","synonyms":"U7.22","biotype":"snRNA","ncbi_id":"100147770","summary":null,"start":32173684,"end":32173744,"strand":1,"description":"RNA, U7 small nuclear 22 pseudogene [Source:HGNC Symbol;Acc:HGNC:34118]"}, {"versioned_ensembl_gene_id":"ENSG00000251726.1","gene_symbol":"RNU7-41P","gene_name":"RNA, U7 small nuclear 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:34137]","synonyms":"U7.41","biotype":"snRNA","ncbi_id":"100147828","summary":null,"start":34845300,"end":34845360,"strand":-1,"description":"RNA, U7 small nuclear 41 pseudogene [Source:HGNC Symbol;Acc:HGNC:34137]"}, {"versioned_ensembl_gene_id":"ENSG00000252760.1","gene_symbol":"RNA5SP54","gene_name":"RNA, 5S ribosomal pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:42831]","synonyms":"RN5S54","biotype":"rRNA","ncbi_id":"100873292","summary":null,"start":111041834,"end":111041925,"strand":1,"description":"RNA, 5S ribosomal pseudogene 54 [Source:HGNC Symbol;Acc:HGNC:42831]"}, {"versioned_ensembl_gene_id":"ENSG00000202290.1","gene_symbol":"RNA5SP37","gene_name":"RNA, 5S ribosomal pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:42613]","synonyms":"RN5S37","biotype":"rRNA","ncbi_id":"100873369","summary":null,"start":97362972,"end":97363101,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 37 [Source:HGNC Symbol;Acc:HGNC:42613]"}, {"versioned_ensembl_gene_id":"ENSG00000207808.1","gene_symbol":"MIR27A","gene_name":"microRNA 27a [Source:HGNC Symbol;Acc:HGNC:31613]","synonyms":"MIRN27A,hsa-mir-27a","biotype":"miRNA","ncbi_id":"407018","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13836440,"end":13836517,"strand":-1,"description":"microRNA 27a [Source:HGNC Symbol;Acc:HGNC:31613]"}, {"versioned_ensembl_gene_id":"ENSG00000200170.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":72220752,"end":72220852,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265418.1","gene_symbol":"MIR4261","gene_name":"microRNA 4261 [Source:HGNC Symbol;Acc:HGNC:38272]","synonyms":"hsa-mir-4261","biotype":"miRNA","ncbi_id":"100422929","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10192614,"end":10192671,"strand":-1,"description":"microRNA 4261 [Source:HGNC Symbol;Acc:HGNC:38272]"}, {"versioned_ensembl_gene_id":"ENSG00000252544.1","gene_symbol":"RNU6-1282P","gene_name":"RNA, U6 small nuclear 1282, pseudogene [Source:HGNC Symbol;Acc:HGNC:48245]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481585","summary":null,"start":151300518,"end":151300613,"strand":1,"description":"RNA, U6 small nuclear 1282, pseudogene [Source:HGNC Symbol;Acc:HGNC:48245]"}, {"versioned_ensembl_gene_id":"ENSG00000199263.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68474553,"end":68474664,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252996.1","gene_symbol":"RNU6-1315P","gene_name":"RNA, U6 small nuclear 1315, pseudogene [Source:HGNC Symbol;Acc:HGNC:48278]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481950","summary":null,"start":2954240,"end":2954338,"strand":-1,"description":"RNA, U6 small nuclear 1315, pseudogene [Source:HGNC Symbol;Acc:HGNC:48278]"}, {"versioned_ensembl_gene_id":"ENSG00000264764.1","gene_symbol":"MIR4772","gene_name":"microRNA 4772 [Source:HGNC Symbol;Acc:HGNC:41741]","synonyms":"hsa-mir-4772","biotype":"miRNA","ncbi_id":"100616157","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":102432289,"end":102432366,"strand":1,"description":"microRNA 4772 [Source:HGNC Symbol;Acc:HGNC:41741]"}, {"versioned_ensembl_gene_id":"ENSG00000283639.1","gene_symbol":"MIR9500","gene_name":"microRNA 9500 [Source:HGNC Symbol;Acc:HGNC:50841]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504730","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":218823090,"end":218823154,"strand":1,"description":"microRNA 9500 [Source:HGNC Symbol;Acc:HGNC:50841]"}, {"versioned_ensembl_gene_id":"ENSG00000222398.1","gene_symbol":"RNU6-554P","gene_name":"RNA, U6 small nuclear 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:47517]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479812","summary":null,"start":43602543,"end":43602648,"strand":1,"description":"RNA, U6 small nuclear 554, pseudogene [Source:HGNC Symbol;Acc:HGNC:47517]"}, {"versioned_ensembl_gene_id":"ENSG00000278217.1","gene_symbol":"MALAT1","gene_name":"Metastasis associated lung adenocarcinoma transcript 1 [Source:RFAM;Acc:RF01871]","synonyms":"MALAT-1,LINC00047,HCN,PRO1073,NEAT2,NCRNA00047,mascRNA","biotype":"misc_RNA","ncbi_id":"378938","summary":"This gene produces a precursor transcript from which a long non-coding RNA is derived by RNase P cleavage of a tRNA-like small ncRNA (known as mascRNA) from its 3' end. The resultant mature transcript lacks a canonical poly(A) tail but is instead stabilized by a 3' triple helical structure. This transcript is retained in the nucleus where it is thought to form molecular scaffolds for ribonucleoprotein complexes. It may act as a transcriptional regulator for numerous genes, including some genes involved in cancer metastasis and cell migration, and it is involved in cell cycle regulation. Its upregulation in multiple cancerous tissues has been associated with the proliferation and metastasis of tumor cells. [provided by RefSeq, Mar 2015]","start":65502914,"end":65503008,"strand":1,"description":"Metastasis associated lung adenocarcinoma transcript 1 [Source:RFAM;Acc:RF01871]"}, {"versioned_ensembl_gene_id":"ENSG00000265841.1","gene_symbol":"MIR548X","gene_name":"microRNA 548x [Source:HGNC Symbol;Acc:HGNC:38248]","synonyms":"hsa-mir-548x","biotype":"miRNA","ncbi_id":"100422920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18686090,"end":18686164,"strand":-1,"description":"microRNA 548x [Source:HGNC Symbol;Acc:HGNC:38248]"}, {"versioned_ensembl_gene_id":"ENSG00000265180.1","gene_symbol":"MIR4790","gene_name":"microRNA 4790 [Source:HGNC Symbol;Acc:HGNC:41820]","synonyms":"hsa-mir-4790","biotype":"miRNA","ncbi_id":"100616334","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5250177,"end":5250255,"strand":-1,"description":"microRNA 4790 [Source:HGNC Symbol;Acc:HGNC:41820]"}, {"versioned_ensembl_gene_id":"ENSG00000201619.1","gene_symbol":"SNORA67","gene_name":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]","synonyms":"U67,RNU67","biotype":"snoRNA","ncbi_id":"26781","summary":null,"start":179201487,"end":179201627,"strand":1,"description":"Small nucleolar RNA SNORA67 [Source:RFAM;Acc:RF00272]"}, {"versioned_ensembl_gene_id":"ENSG00000275789.1","gene_symbol":"MIR8064","gene_name":"microRNA 8064 [Source:HGNC Symbol;Acc:HGNC:50236]","synonyms":"hsa-mir-8064","biotype":"miRNA","ncbi_id":"102465866","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":52846463,"end":52846552,"strand":-1,"description":"microRNA 8064 [Source:HGNC Symbol;Acc:HGNC:50236]"}, {"versioned_ensembl_gene_id":"ENSG00000207137.1","gene_symbol":"SNORD116-13","gene_name":"small nucleolar RNA, C/D box 116-13 [Source:HGNC Symbol;Acc:HGNC:33079]","synonyms":"HBII-85-13","biotype":"snoRNA","ncbi_id":"100033425","summary":null,"start":25079058,"end":25079149,"strand":1,"description":"small nucleolar RNA, C/D box 116-13 [Source:HGNC Symbol;Acc:HGNC:33079]"}, {"versioned_ensembl_gene_id":"ENSG00000252677.1","gene_symbol":"SNORA81","gene_name":"Small nucleolar RNA SNORA81 [Source:RFAM;Acc:RF01241]","synonyms":"HBI-61","biotype":"snoRNA","ncbi_id":"677847","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA81, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":21711950,"end":21712119,"strand":-1,"description":"Small nucleolar RNA SNORA81 [Source:RFAM;Acc:RF01241]"}, {"versioned_ensembl_gene_id":"ENSG00000266863.2","gene_symbol":"RN7SL123P","gene_name":"RNA, 7SL, cytoplasmic 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:46139]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479266","summary":null,"start":6661651,"end":6661942,"strand":1,"description":"RNA, 7SL, cytoplasmic 123, pseudogene [Source:HGNC Symbol;Acc:HGNC:46139]"}, {"versioned_ensembl_gene_id":"ENSG00000265829.1","gene_symbol":"MIR548AG1","gene_name":"microRNA 548ag-1 [Source:HGNC Symbol;Acc:HGNC:41625]","synonyms":"hsa-mir-548ag-1","biotype":"miRNA","ncbi_id":"100616450","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60922619,"end":60922684,"strand":1,"description":"microRNA 548ag-1 [Source:HGNC Symbol;Acc:HGNC:41625]"}, {"versioned_ensembl_gene_id":"ENSG00000199169.1","gene_symbol":"MIR367","gene_name":"microRNA 367 [Source:HGNC Symbol;Acc:HGNC:31781]","synonyms":"MIRN367,hsa-mir-367","biotype":"miRNA","ncbi_id":"442912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":112647874,"end":112647941,"strand":-1,"description":"microRNA 367 [Source:HGNC Symbol;Acc:HGNC:31781]"}, {"versioned_ensembl_gene_id":"ENSG00000207473.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73346936,"end":73347048,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264341.1","gene_symbol":"MIR4417","gene_name":"microRNA 4417 [Source:HGNC Symbol;Acc:HGNC:41535]","synonyms":"hsa-mir-4417","biotype":"miRNA","ncbi_id":"100616489","summary":"This record was withdrawn by miRBase.","start":5564071,"end":5564143,"strand":1,"description":"microRNA 4417 [Source:HGNC Symbol;Acc:HGNC:41535]"}, {"versioned_ensembl_gene_id":"ENSG00000263679.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31573052,"end":31573153,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252148.1","gene_symbol":"RNU6-1206P","gene_name":"RNA, U6 small nuclear 1206, pseudogene [Source:HGNC Symbol;Acc:HGNC:48169]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481561","summary":null,"start":201079842,"end":201079944,"strand":1,"description":"RNA, U6 small nuclear 1206, pseudogene [Source:HGNC Symbol;Acc:HGNC:48169]"}, {"versioned_ensembl_gene_id":"ENSG00000264105.1","gene_symbol":"MIR3688-1","gene_name":"microRNA 3688-1 [Source:HGNC Symbol;Acc:HGNC:38986]","synonyms":"MIR3688,hsa-mir-3688-1,hsa-mir-3688","biotype":"miRNA","ncbi_id":"100500881","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159128802,"end":159128894,"strand":-1,"description":"microRNA 3688-1 [Source:HGNC Symbol;Acc:HGNC:38986]"}, {"versioned_ensembl_gene_id":"ENSG00000221230.1","gene_symbol":"MIR548L","gene_name":"microRNA 548l [Source:HGNC Symbol;Acc:HGNC:35292]","synonyms":"MIRN548L,hsa-mir-548l","biotype":"miRNA","ncbi_id":"100302275","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94466495,"end":94466580,"strand":-1,"description":"microRNA 548l [Source:HGNC Symbol;Acc:HGNC:35292]"}, {"versioned_ensembl_gene_id":"ENSG00000207407.1","gene_symbol":"SNORA1","gene_name":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]","synonyms":"ACA1","biotype":"snoRNA","ncbi_id":"677792","summary":null,"start":19591156,"end":19591291,"strand":-1,"description":"Small nucleolar RNA SNORA1 [Source:RFAM;Acc:RF00408]"}, {"versioned_ensembl_gene_id":"ENSG00000278571.1","gene_symbol":"MIR7161","gene_name":"microRNA 7161 [Source:HGNC Symbol;Acc:HGNC:49985]","synonyms":"hsa-mir-7161","biotype":"miRNA","ncbi_id":"102465694","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":158609707,"end":158609790,"strand":1,"description":"microRNA 7161 [Source:HGNC Symbol;Acc:HGNC:49985]"}, {"versioned_ensembl_gene_id":"ENSG00000251798.1","gene_symbol":"RNU6-863P","gene_name":"RNA, U6 small nuclear 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:47826]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481453","summary":null,"start":76087444,"end":76087547,"strand":1,"description":"RNA, U6 small nuclear 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:47826]"}, {"versioned_ensembl_gene_id":"ENSG00000199179.3","gene_symbol":"MIRLET7I","gene_name":"microRNA let-7i [Source:HGNC Symbol;Acc:HGNC:31486]","synonyms":"MIRNLET7I,hsa-let-7i","biotype":"miRNA","ncbi_id":"406891","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62603686,"end":62603769,"strand":1,"description":"microRNA let-7i [Source:HGNC Symbol;Acc:HGNC:31486]"}, {"versioned_ensembl_gene_id":"ENSG00000252509.1","gene_symbol":"RNA5SP271","gene_name":"RNA, 5S ribosomal pseudogene 271 [Source:HGNC Symbol;Acc:HGNC:43171]","synonyms":"RN5S271","biotype":"rRNA","ncbi_id":"100873524","summary":null,"start":72357728,"end":72357815,"strand":1,"description":"RNA, 5S ribosomal pseudogene 271 [Source:HGNC Symbol;Acc:HGNC:43171]"}, {"versioned_ensembl_gene_id":"ENSG00000207628.3","gene_symbol":"MIR651","gene_name":"microRNA 651 [Source:HGNC Symbol;Acc:HGNC:32907]","synonyms":"MIRN651,hsa-mir-651","biotype":"miRNA","ncbi_id":"723779","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8126965,"end":8127061,"strand":1,"description":"microRNA 651 [Source:HGNC Symbol;Acc:HGNC:32907]"}, {"versioned_ensembl_gene_id":"ENSG00000253003.1","gene_symbol":"RNU6-1261P","gene_name":"RNA, U6 small nuclear 1261, pseudogene [Source:HGNC Symbol;Acc:HGNC:48224]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480116","summary":null,"start":34675891,"end":34675994,"strand":1,"description":"RNA, U6 small nuclear 1261, pseudogene [Source:HGNC Symbol;Acc:HGNC:48224]"}, {"versioned_ensembl_gene_id":"ENSG00000284584.1","gene_symbol":"MIR5006","gene_name":"microRNA 5006 [Source:HGNC Symbol;Acc:HGNC:43495]","synonyms":"hsa-mir-5006","biotype":"miRNA","ncbi_id":"100847026","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41568286,"end":41568395,"strand":-1,"description":"microRNA 5006 [Source:HGNC Symbol;Acc:HGNC:43495]"}, {"versioned_ensembl_gene_id":"ENSG00000221494.1","gene_symbol":"MIR548I4","gene_name":"microRNA 548i-4 [Source:HGNC Symbol;Acc:HGNC:35355]","synonyms":"MIRN548I4,hsa-mir-548i-4","biotype":"miRNA","ncbi_id":"100302191","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":84225752,"end":84225828,"strand":-1,"description":"microRNA 548i-4 [Source:HGNC Symbol;Acc:HGNC:35355]"}, {"versioned_ensembl_gene_id":"ENSG00000222715.1","gene_symbol":"MIR1911","gene_name":"microRNA 1911 [Source:HGNC Symbol;Acc:HGNC:35395]","synonyms":"MIRN1911,hsa-mir-1911","biotype":"miRNA","ncbi_id":"100302222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114763184,"end":114763263,"strand":1,"description":"microRNA 1911 [Source:HGNC Symbol;Acc:HGNC:35395]"}, {"versioned_ensembl_gene_id":"ENSG00000200011.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93460725,"end":93460826,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265450.1","gene_symbol":"MIR4502","gene_name":"microRNA 4502 [Source:HGNC Symbol;Acc:HGNC:41534]","synonyms":"hsa-mir-4502","biotype":"miRNA","ncbi_id":"100616227","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114273828,"end":114273908,"strand":1,"description":"microRNA 4502 [Source:HGNC Symbol;Acc:HGNC:41534]"}, {"versioned_ensembl_gene_id":"ENSG00000207455.1","gene_symbol":"RNU6-331P","gene_name":"RNA, U6 small nuclear 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:47294]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479713","summary":null,"start":29899587,"end":29899693,"strand":-1,"description":"RNA, U6 small nuclear 331, pseudogene [Source:HGNC Symbol;Acc:HGNC:47294]"}, {"versioned_ensembl_gene_id":"ENSG00000206640.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":185257911,"end":185258015,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283279.1","gene_symbol":"MIR376C","gene_name":"microRNA 376c [Source:HGNC Symbol;Acc:HGNC:31782]","synonyms":"MIRN376C,MIRN368,hsa-mir-376c,hsa-mir-368","biotype":"miRNA","ncbi_id":"442913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101039690,"end":101039755,"strand":1,"description":"microRNA 376c [Source:HGNC Symbol;Acc:HGNC:31782]"}, {"versioned_ensembl_gene_id":"ENSG00000243723.3","gene_symbol":"RN7SL393P","gene_name":"RNA, 7SL, cytoplasmic 393, pseudogene [Source:HGNC Symbol;Acc:HGNC:46409]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481756","summary":null,"start":158447166,"end":158447461,"strand":-1,"description":"RNA, 7SL, cytoplasmic 393, pseudogene [Source:HGNC Symbol;Acc:HGNC:46409]"}, {"versioned_ensembl_gene_id":"ENSG00000206882.1","gene_symbol":"RNA5SP87","gene_name":"RNA, 5S ribosomal pseudogene 87 [Source:HGNC Symbol;Acc:HGNC:42885]","synonyms":"RN5S87","biotype":"rRNA","ncbi_id":"100873320","summary":null,"start":22338886,"end":22339003,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 87 [Source:HGNC Symbol;Acc:HGNC:42885]"}, {"versioned_ensembl_gene_id":"ENSG00000265098.3","gene_symbol":"MIR4510","gene_name":"microRNA 4510 [Source:HGNC Symbol;Acc:HGNC:41708]","synonyms":"hsa-mir-4510","biotype":"miRNA","ncbi_id":"100616293","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35926856,"end":35926923,"strand":1,"description":"microRNA 4510 [Source:HGNC Symbol;Acc:HGNC:41708]"}, {"versioned_ensembl_gene_id":"ENSG00000207495.1","gene_symbol":"RNY3P10","gene_name":"RNA, Ro-associated Y3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42494]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873820","summary":null,"start":69802940,"end":69803041,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42494]"}, {"versioned_ensembl_gene_id":"ENSG00000199475.1","gene_symbol":"RN7SKP104","gene_name":"RNA, 7SK small nuclear pseudogene 104 [Source:HGNC Symbol;Acc:HGNC:45828]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480865","summary":null,"start":97598933,"end":97599260,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 104 [Source:HGNC Symbol;Acc:HGNC:45828]"}, {"versioned_ensembl_gene_id":"ENSG00000263857.1","gene_symbol":"MIR4729","gene_name":"microRNA 4729 [Source:HGNC Symbol;Acc:HGNC:41585]","synonyms":"hsa-mir-4729","biotype":"miRNA","ncbi_id":"100616204","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59366083,"end":59366154,"strand":1,"description":"microRNA 4729 [Source:HGNC Symbol;Acc:HGNC:41585]"}, {"versioned_ensembl_gene_id":"ENSG00000206582.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34526510,"end":34526606,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274230.1","gene_symbol":"RMST_3","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 3 [Source:RFAM;Acc:RF01964]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97493178,"end":97493286,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 3 [Source:RFAM;Acc:RF01964]"}, {"versioned_ensembl_gene_id":"ENSG00000283604.1","gene_symbol":"MIR338","gene_name":"microRNA 338 [Source:HGNC Symbol;Acc:HGNC:31775]","synonyms":"MIRN338,hsa-mir-338","biotype":"miRNA","ncbi_id":"442906","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81125883,"end":81125949,"strand":-1,"description":"microRNA 338 [Source:HGNC Symbol;Acc:HGNC:31775]"}, {"versioned_ensembl_gene_id":"ENSG00000274262.1","gene_symbol":"7SK","gene_name":"7SK RNA [Source:RFAM;Acc:RF00100]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35889558,"end":35889804,"strand":1,"description":"7SK RNA [Source:RFAM;Acc:RF00100]"}, {"versioned_ensembl_gene_id":"ENSG00000207613.1","gene_symbol":"MIR181C","gene_name":"microRNA 181c [Source:HGNC Symbol;Acc:HGNC:31552]","synonyms":"MIRN181C,hsa-mir-181c","biotype":"miRNA","ncbi_id":"406957","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13874699,"end":13874808,"strand":1,"description":"microRNA 181c [Source:HGNC Symbol;Acc:HGNC:31552]"}, {"versioned_ensembl_gene_id":"ENSG00000278569.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17205652,"end":17205928,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000238680.1","gene_symbol":"RNU6-1037P","gene_name":"RNA, U6 small nuclear 1037, pseudogene [Source:HGNC Symbol;Acc:HGNC:48000]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481508","summary":null,"start":66946116,"end":66946222,"strand":1,"description":"RNA, U6 small nuclear 1037, pseudogene [Source:HGNC Symbol;Acc:HGNC:48000]"}, {"versioned_ensembl_gene_id":"ENSG00000283212.1","gene_symbol":"MIR642B","gene_name":"microRNA 642b [Source:HGNC Symbol;Acc:HGNC:38902]","synonyms":"hsa-mir-642b","biotype":"miRNA","ncbi_id":"100500845","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45674932,"end":45675008,"strand":-1,"description":"microRNA 642b [Source:HGNC Symbol;Acc:HGNC:38902]"}, {"versioned_ensembl_gene_id":"ENSG00000264676.2","gene_symbol":"RN7SL204P","gene_name":"RNA, 7SL, cytoplasmic 204, pseudogene [Source:HGNC Symbol;Acc:HGNC:46220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480977","summary":null,"start":236072295,"end":236072556,"strand":1,"description":"RNA, 7SL, cytoplasmic 204, pseudogene [Source:HGNC Symbol;Acc:HGNC:46220]"}, {"versioned_ensembl_gene_id":"ENSG00000202412.1","gene_symbol":"RNY3P13","gene_name":"RNA, Ro-associated Y3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50889]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481714","summary":null,"start":129818932,"end":129819033,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:50889]"}, {"versioned_ensembl_gene_id":"ENSG00000201165.1","gene_symbol":"RNU6-1229P","gene_name":"RNA, U6 small nuclear 1229, pseudogene [Source:HGNC Symbol;Acc:HGNC:48192]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481568","summary":null,"start":65023204,"end":65023310,"strand":-1,"description":"RNA, U6 small nuclear 1229, pseudogene [Source:HGNC Symbol;Acc:HGNC:48192]"}, {"versioned_ensembl_gene_id":"ENSG00000252260.1","gene_symbol":"RNA5SP461","gene_name":"RNA, 5S ribosomal pseudogene 461 [Source:HGNC Symbol;Acc:HGNC:43361]","synonyms":"RN5S461","biotype":"rRNA","ncbi_id":"100873705","summary":null,"start":77863464,"end":77863567,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 461 [Source:HGNC Symbol;Acc:HGNC:43361]"}, {"versioned_ensembl_gene_id":"ENSG00000207767.3","gene_symbol":"MIR516A1","gene_name":"microRNA 516a-1 [Source:HGNC Symbol;Acc:HGNC:32130]","synonyms":"hsa-mir-516-1,MIRN516A1,MIRN516-1,hsa-mir-516a-1","biotype":"miRNA","ncbi_id":"574498","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53756741,"end":53756830,"strand":1,"description":"microRNA 516a-1 [Source:HGNC Symbol;Acc:HGNC:32130]"}, {"versioned_ensembl_gene_id":"ENSG00000239001.1","gene_symbol":"RNU6-420P","gene_name":"RNA, U6 small nuclear 420, pseudogene [Source:HGNC Symbol;Acc:HGNC:47383]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481769","summary":null,"start":22118983,"end":22119089,"strand":1,"description":"RNA, U6 small nuclear 420, pseudogene [Source:HGNC Symbol;Acc:HGNC:47383]"}, {"versioned_ensembl_gene_id":"ENSG00000223217.1","gene_symbol":"RNU6-938P","gene_name":"RNA, U6 small nuclear 938, pseudogene [Source:HGNC Symbol;Acc:HGNC:47901]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479981","summary":null,"start":75409086,"end":75409188,"strand":-1,"description":"RNA, U6 small nuclear 938, pseudogene [Source:HGNC Symbol;Acc:HGNC:47901]"}, {"versioned_ensembl_gene_id":"ENSG00000266097.1","gene_symbol":"MIR5192","gene_name":"microRNA 5192 [Source:HGNC Symbol;Acc:HGNC:43473]","synonyms":"hsa-mir-5192","biotype":"miRNA","ncbi_id":"100847087","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62205826,"end":62205917,"strand":1,"description":"microRNA 5192 [Source:HGNC Symbol;Acc:HGNC:43473]"}, {"versioned_ensembl_gene_id":"ENSG00000264525.1","gene_symbol":"MIR4778","gene_name":"microRNA 4778 [Source:HGNC Symbol;Acc:HGNC:41648]","synonyms":"hsa-mir-4778","biotype":"miRNA","ncbi_id":"100616464","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66358249,"end":66358328,"strand":-1,"description":"microRNA 4778 [Source:HGNC Symbol;Acc:HGNC:41648]"}, {"versioned_ensembl_gene_id":"ENSG00000206822.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63621760,"end":63621871,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201794.1","gene_symbol":"RN7SKP130","gene_name":"RNA, 7SK small nuclear pseudogene 130 [Source:HGNC Symbol;Acc:HGNC:45854]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480873","summary":null,"start":2999094,"end":2999394,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 130 [Source:HGNC Symbol;Acc:HGNC:45854]"}, {"versioned_ensembl_gene_id":"ENSG00000206780.1","gene_symbol":"SNORA75B","gene_name":"small nucleolar RNA, H/ACA box 75B [Source:HGNC Symbol;Acc:HGNC:52220]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616994","summary":null,"start":17320746,"end":17320882,"strand":-1,"description":"small nucleolar RNA, H/ACA box 75B [Source:HGNC Symbol;Acc:HGNC:52220]"}, {"versioned_ensembl_gene_id":"ENSG00000263828.1","gene_symbol":"MIR4439","gene_name":"microRNA 4439 [Source:HGNC Symbol;Acc:HGNC:41622]","synonyms":"hsa-mir-4439","biotype":"miRNA","ncbi_id":"100616207","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":225010461,"end":225010540,"strand":-1,"description":"microRNA 4439 [Source:HGNC Symbol;Acc:HGNC:41622]"}, {"versioned_ensembl_gene_id":"ENSG00000223118.1","gene_symbol":"RN7SKP102","gene_name":"RNA, 7SK small nuclear pseudogene 102 [Source:HGNC Symbol;Acc:HGNC:45826]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481810","summary":null,"start":123869256,"end":123869570,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 102 [Source:HGNC Symbol;Acc:HGNC:45826]"}, {"versioned_ensembl_gene_id":"ENSG00000278218.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":11148584,"end":11148769,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000283474.1","gene_symbol":"MIR6828","gene_name":"microRNA 6828 [Source:HGNC Symbol;Acc:HGNC:50057]","synonyms":"hsa-mir-6828","biotype":"miRNA","ncbi_id":"102465497","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":170423103,"end":170423162,"strand":1,"description":"microRNA 6828 [Source:HGNC Symbol;Acc:HGNC:50057]"}, {"versioned_ensembl_gene_id":"ENSG00000199920.1","gene_symbol":"RNU4-44P","gene_name":"RNA, U4 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:46980]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479578","summary":null,"start":134760208,"end":134760348,"strand":-1,"description":"RNA, U4 small nuclear 44, pseudogene [Source:HGNC Symbol;Acc:HGNC:46980]"}, {"versioned_ensembl_gene_id":"ENSG00000239560.3","gene_symbol":"RN7SL479P","gene_name":"RNA, 7SL, cytoplasmic 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:46495]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479398","summary":null,"start":44117098,"end":44117397,"strand":-1,"description":"RNA, 7SL, cytoplasmic 479, pseudogene [Source:HGNC Symbol;Acc:HGNC:46495]"}, {"versioned_ensembl_gene_id":"ENSG00000238523.1","gene_symbol":"RNU7-107P","gene_name":"RNA, U7 small nuclear 107 pseudogene [Source:HGNC Symbol;Acc:HGNC:45641]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479067","summary":null,"start":50590652,"end":50590712,"strand":-1,"description":"RNA, U7 small nuclear 107 pseudogene [Source:HGNC Symbol;Acc:HGNC:45641]"}, {"versioned_ensembl_gene_id":"ENSG00000265850.1","gene_symbol":"MIR4797","gene_name":"microRNA 4797 [Source:HGNC Symbol;Acc:HGNC:41758]","synonyms":"hsa-mir-4797","biotype":"miRNA","ncbi_id":"100616216","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":197293878,"end":197293948,"strand":-1,"description":"microRNA 4797 [Source:HGNC Symbol;Acc:HGNC:41758]"}, {"versioned_ensembl_gene_id":"ENSG00000201474.1","gene_symbol":"RNU6-164P","gene_name":"RNA, U6 small nuclear 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:47127]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479639","summary":null,"start":162477891,"end":162477993,"strand":1,"description":"RNA, U6 small nuclear 164, pseudogene [Source:HGNC Symbol;Acc:HGNC:47127]"}, {"versioned_ensembl_gene_id":"ENSG00000265623.1","gene_symbol":"MIR3139","gene_name":"microRNA 3139 [Source:HGNC Symbol;Acc:HGNC:38201]","synonyms":"hsa-mir-3139","biotype":"miRNA","ncbi_id":"100423017","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143343460,"end":143343535,"strand":1,"description":"microRNA 3139 [Source:HGNC Symbol;Acc:HGNC:38201]"}, {"versioned_ensembl_gene_id":"ENSG00000278438.1","gene_symbol":"MIR7849","gene_name":"microRNA 7849 [Source:HGNC Symbol;Acc:HGNC:50166]","synonyms":"hsa-mir-7849","biotype":"miRNA","ncbi_id":"102465837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":146408583,"end":146408688,"strand":1,"description":"microRNA 7849 [Source:HGNC Symbol;Acc:HGNC:50166]"}, {"versioned_ensembl_gene_id":"ENSG00000222051.1","gene_symbol":"RNU6-1165P","gene_name":"RNA, U6 small nuclear 1165, pseudogene [Source:HGNC Symbol;Acc:HGNC:48128]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480079","summary":null,"start":101622859,"end":101622965,"strand":1,"description":"RNA, U6 small nuclear 1165, pseudogene [Source:HGNC Symbol;Acc:HGNC:48128]"}, {"versioned_ensembl_gene_id":"ENSG00000283572.1","gene_symbol":"MIR4251","gene_name":"microRNA 4251 [Source:HGNC Symbol;Acc:HGNC:38370]","synonyms":"hsa-mir-4251","biotype":"miRNA","ncbi_id":"100422968","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3127975,"end":3128035,"strand":1,"description":"microRNA 4251 [Source:HGNC Symbol;Acc:HGNC:38370]"}, {"versioned_ensembl_gene_id":"ENSG00000251804.1","gene_symbol":"RNU6-1294P","gene_name":"RNA, U6 small nuclear 1294, pseudogene [Source:HGNC Symbol;Acc:HGNC:48257]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480131","summary":null,"start":142407657,"end":142407737,"strand":-1,"description":"RNA, U6 small nuclear 1294, pseudogene [Source:HGNC Symbol;Acc:HGNC:48257]"}, {"versioned_ensembl_gene_id":"ENSG00000284000.1","gene_symbol":"MIR4458","gene_name":"microRNA 4458 [Source:HGNC Symbol;Acc:HGNC:41674]","synonyms":"hsa-mir-4458","biotype":"miRNA","ncbi_id":"100616142","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8460925,"end":8460999,"strand":1,"description":"microRNA 4458 [Source:HGNC Symbol;Acc:HGNC:41674]"}, {"versioned_ensembl_gene_id":"ENSG00000266321.1","gene_symbol":"MIR4293","gene_name":"microRNA 4293 [Source:HGNC Symbol;Acc:HGNC:38270]","synonyms":"hsa-mir-4293","biotype":"miRNA","ncbi_id":"100422843","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14383200,"end":14383277,"strand":-1,"description":"microRNA 4293 [Source:HGNC Symbol;Acc:HGNC:38270]"}, {"versioned_ensembl_gene_id":"ENSG00000238619.1","gene_symbol":"RNU6-775P","gene_name":"RNA, U6 small nuclear 775, pseudogene [Source:HGNC Symbol;Acc:HGNC:47738]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479909","summary":null,"start":55451004,"end":55451099,"strand":-1,"description":"RNA, U6 small nuclear 775, pseudogene [Source:HGNC Symbol;Acc:HGNC:47738]"}, {"versioned_ensembl_gene_id":"ENSG00000206871.1","gene_symbol":"RNU6-533P","gene_name":"RNA, U6 small nuclear 533, pseudogene [Source:HGNC Symbol;Acc:HGNC:47496]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481901","summary":null,"start":36309584,"end":36309690,"strand":-1,"description":"RNA, U6 small nuclear 533, pseudogene [Source:HGNC Symbol;Acc:HGNC:47496]"}, {"versioned_ensembl_gene_id":"ENSG00000276866.1","gene_symbol":"MIR7151","gene_name":"microRNA 7151 [Source:HGNC Symbol;Acc:HGNC:50170]","synonyms":"hsa-mir-7151","biotype":"miRNA","ncbi_id":"102466814","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67403351,"end":67403410,"strand":-1,"description":"microRNA 7151 [Source:HGNC Symbol;Acc:HGNC:50170]"}, {"versioned_ensembl_gene_id":"ENSG00000222958.1","gene_symbol":"MIR1913","gene_name":"microRNA 1913 [Source:HGNC Symbol;Acc:HGNC:35397]","synonyms":"MIRN1913,hsa-mir-1913","biotype":"miRNA","ncbi_id":"100302141","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":166509354,"end":166509433,"strand":-1,"description":"microRNA 1913 [Source:HGNC Symbol;Acc:HGNC:35397]"}, {"versioned_ensembl_gene_id":"ENSG00000223125.1","gene_symbol":"RNU2-32P","gene_name":"RNA, U2 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:48525]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481644","summary":null,"start":41467956,"end":41468146,"strand":1,"description":"RNA, U2 small nuclear 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:48525]"}, {"versioned_ensembl_gene_id":"ENSG00000212289.1","gene_symbol":"RNA5SP339","gene_name":"RNA, 5S ribosomal pseudogene 339 [Source:HGNC Symbol;Acc:HGNC:43239]","synonyms":"RN5S339","biotype":"rRNA","ncbi_id":"100873602","summary":null,"start":27521605,"end":27521726,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 339 [Source:HGNC Symbol;Acc:HGNC:43239]"}, {"versioned_ensembl_gene_id":"ENSG00000222321.1","gene_symbol":"MIR1912","gene_name":"microRNA 1912 [Source:HGNC Symbol;Acc:HGNC:35396]","synonyms":"MIRN1912,hsa-mir-1912","biotype":"miRNA","ncbi_id":"100302144","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114651544,"end":114651623,"strand":1,"description":"microRNA 1912 [Source:HGNC Symbol;Acc:HGNC:35396]"}, {"versioned_ensembl_gene_id":"ENSG00000284594.1","gene_symbol":"MIR7847","gene_name":"microRNA 7847 [Source:HGNC Symbol;Acc:HGNC:50153]","synonyms":"hsa-mir-7847","biotype":"miRNA","ncbi_id":"102465993","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1880045,"end":1880147,"strand":1,"description":"microRNA 7847 [Source:HGNC Symbol;Acc:HGNC:50153]"}, {"versioned_ensembl_gene_id":"ENSG00000238936.1","gene_symbol":"SNORD65B","gene_name":"small nucleolar RNA, C/D box 65B [Source:HGNC Symbol;Acc:HGNC:52231]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616980","summary":null,"start":41426655,"end":41426727,"strand":1,"description":"small nucleolar RNA, C/D box 65B [Source:HGNC Symbol;Acc:HGNC:52231]"}, {"versioned_ensembl_gene_id":"ENSG00000278793.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":127840,"end":127946,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000221463.3","gene_symbol":"MIR1277","gene_name":"microRNA 1277 [Source:HGNC Symbol;Acc:HGNC:35350]","synonyms":"MIRN1277,hsa-mir-1277","biotype":"miRNA","ncbi_id":"100302214","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":118386394,"end":118386471,"strand":1,"description":"microRNA 1277 [Source:HGNC Symbol;Acc:HGNC:35350]"}, {"versioned_ensembl_gene_id":"ENSG00000206605.1","gene_symbol":"RNU6-946P","gene_name":"RNA, U6 small nuclear 946, pseudogene [Source:HGNC Symbol;Acc:HGNC:47909]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481478","summary":null,"start":26790540,"end":26790646,"strand":-1,"description":"RNA, U6 small nuclear 946, pseudogene [Source:HGNC Symbol;Acc:HGNC:47909]"}, {"versioned_ensembl_gene_id":"ENSG00000265227.1","gene_symbol":"MIR4699","gene_name":"microRNA 4699 [Source:HGNC Symbol;Acc:HGNC:41636]","synonyms":"hsa-mir-4699","biotype":"miRNA","ncbi_id":"100616133","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81158388,"end":81158461,"strand":1,"description":"microRNA 4699 [Source:HGNC Symbol;Acc:HGNC:41636]"}, {"versioned_ensembl_gene_id":"ENSG00000212249.2","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":68873954,"end":68874087,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000199905.1","gene_symbol":"RNU6-492P","gene_name":"RNA, U6 small nuclear 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:47455]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481335","summary":null,"start":107475036,"end":107475139,"strand":-1,"description":"RNA, U6 small nuclear 492, pseudogene [Source:HGNC Symbol;Acc:HGNC:47455]"}, {"versioned_ensembl_gene_id":"ENSG00000206688.1","gene_symbol":"SNORD116-18","gene_name":"small nucleolar RNA, C/D box 116-18 [Source:HGNC Symbol;Acc:HGNC:33084]","synonyms":"HBII-85-18","biotype":"snoRNA","ncbi_id":"100033430","summary":null,"start":25085385,"end":25085476,"strand":1,"description":"small nucleolar RNA, C/D box 116-18 [Source:HGNC Symbol;Acc:HGNC:33084]"}, {"versioned_ensembl_gene_id":"ENSG00000252695.1","gene_symbol":"MIR2276","gene_name":"microRNA 2276 [Source:HGNC Symbol;Acc:HGNC:37313]","synonyms":"hsa-mir-2276","biotype":"miRNA","ncbi_id":"100313842","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24162416,"end":24162504,"strand":1,"description":"microRNA 2276 [Source:HGNC Symbol;Acc:HGNC:37313]"}, {"versioned_ensembl_gene_id":"ENSG00000207243.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":178554,"end":178656,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252548.1","gene_symbol":"RNU7-149P","gene_name":"RNA, U7 small nuclear 149 pseudogene [Source:HGNC Symbol;Acc:HGNC:45683]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479080","summary":null,"start":98966815,"end":98966873,"strand":-1,"description":"RNA, U7 small nuclear 149 pseudogene [Source:HGNC Symbol;Acc:HGNC:45683]"}, {"versioned_ensembl_gene_id":"ENSG00000221739.1","gene_symbol":"MIR1203","gene_name":"microRNA 1203 [Source:HGNC Symbol;Acc:HGNC:35269]","synonyms":"MIRN1203,hsa-mir-1203","biotype":"miRNA","ncbi_id":"100302211","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48156427,"end":48156511,"strand":-1,"description":"microRNA 1203 [Source:HGNC Symbol;Acc:HGNC:35269]"}, {"versioned_ensembl_gene_id":"ENSG00000276036.1","gene_symbol":"RNA5SP440","gene_name":"RNA, 5S ribosomal pseudogene 440 [Source:HGNC Symbol;Acc:HGNC:43340]","synonyms":"RN5S440","biotype":"rRNA","ncbi_id":"100873688","summary":null,"start":38731802,"end":38731920,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 440 [Source:HGNC Symbol;Acc:HGNC:43340]"}, {"versioned_ensembl_gene_id":"ENSG00000264352.2","gene_symbol":"RN7SL602P","gene_name":"RNA, 7SL, cytoplasmic 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:46618]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479441","summary":null,"start":34809233,"end":34809556,"strand":-1,"description":"RNA, 7SL, cytoplasmic 602, pseudogene [Source:HGNC Symbol;Acc:HGNC:46618]"}, {"versioned_ensembl_gene_id":"ENSG00000284258.1","gene_symbol":"MIR8085","gene_name":"microRNA 8085 [Source:HGNC Symbol;Acc:HGNC:50120]","synonyms":"hsa-mir-8085","biotype":"miRNA","ncbi_id":"102465879","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44758657,"end":44758721,"strand":1,"description":"microRNA 8085 [Source:HGNC Symbol;Acc:HGNC:50120]"}, {"versioned_ensembl_gene_id":"ENSG00000222146.1","gene_symbol":"RNU4-37P","gene_name":"RNA, U4 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46973]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481183","summary":null,"start":112148742,"end":112148825,"strand":-1,"description":"RNA, U4 small nuclear 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46973]"}, {"versioned_ensembl_gene_id":"ENSG00000223223.1","gene_symbol":"RN7SKP192","gene_name":"RNA, 7SK small nuclear pseudogene 192 [Source:HGNC Symbol;Acc:HGNC:45916]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480892","summary":null,"start":59706057,"end":59706383,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 192 [Source:HGNC Symbol;Acc:HGNC:45916]"}, {"versioned_ensembl_gene_id":"ENSG00000274086.1","gene_symbol":"FMR1-AS1_2","gene_name":"FMR1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02118]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":147911822,"end":147911948,"strand":1,"description":"FMR1 antisense RNA 1 conserved region 2 [Source:RFAM;Acc:RF02118]"}, {"versioned_ensembl_gene_id":"ENSG00000208008.1","gene_symbol":"MIR125A","gene_name":"microRNA 125a [Source:HGNC Symbol;Acc:HGNC:31505]","synonyms":"MIRN125A,hsa-mir-125a","biotype":"miRNA","ncbi_id":"406910","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51693254,"end":51693339,"strand":1,"description":"microRNA 125a [Source:HGNC Symbol;Acc:HGNC:31505]"}, {"versioned_ensembl_gene_id":"ENSG00000283490.1","gene_symbol":"MIR518C","gene_name":"microRNA 518c [Source:HGNC Symbol;Acc:HGNC:32109]","synonyms":"MIRN518C,hsa-mir-518c","biotype":"miRNA","ncbi_id":"574477","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53708735,"end":53708835,"strand":1,"description":"microRNA 518c [Source:HGNC Symbol;Acc:HGNC:32109]"}, {"versioned_ensembl_gene_id":"ENSG00000252872.1","gene_symbol":"RNU7-188P","gene_name":"RNA, U7 small nuclear 188 pseudogene [Source:HGNC Symbol;Acc:HGNC:45722]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480832","summary":null,"start":96377857,"end":96377920,"strand":1,"description":"RNA, U7 small nuclear 188 pseudogene [Source:HGNC Symbol;Acc:HGNC:45722]"}, {"versioned_ensembl_gene_id":"ENSG00000265409.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31744327,"end":31744429,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000240116.3","gene_symbol":"RN7SL303P","gene_name":"RNA, 7SL, cytoplasmic 303, pseudogene [Source:HGNC Symbol;Acc:HGNC:46319]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481005","summary":null,"start":22977877,"end":22978127,"strand":1,"description":"RNA, 7SL, cytoplasmic 303, pseudogene [Source:HGNC Symbol;Acc:HGNC:46319]"}, {"versioned_ensembl_gene_id":"ENSG00000274660.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100666695,"end":100667009,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222343.1","gene_symbol":"RN7SKP139","gene_name":"RNA, 7SK small nuclear pseudogene 139 [Source:HGNC Symbol;Acc:HGNC:45863]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480876","summary":null,"start":47272597,"end":47272889,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 139 [Source:HGNC Symbol;Acc:HGNC:45863]"}, {"versioned_ensembl_gene_id":"ENSG00000206832.1","gene_symbol":"RNU6V","gene_name":"RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence [Source:HGNC Symbol;Acc:HGNC:10230]","synonyms":"LH87,87U6","biotype":"snRNA","ncbi_id":"6071","summary":null,"start":109591534,"end":109591640,"strand":-1,"description":"RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence [Source:HGNC Symbol;Acc:HGNC:10230]"}, {"versioned_ensembl_gene_id":"ENSG00000222087.1","gene_symbol":"RNU6-721P","gene_name":"RNA, U6 small nuclear 721, pseudogene [Source:HGNC Symbol;Acc:HGNC:47684]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481774","summary":null,"start":15320840,"end":15320944,"strand":-1,"description":"RNA, U6 small nuclear 721, pseudogene [Source:HGNC Symbol;Acc:HGNC:47684]"}, {"versioned_ensembl_gene_id":"ENSG00000207699.1","gene_symbol":"MIR518A2","gene_name":"microRNA 518a-2 [Source:HGNC Symbol;Acc:HGNC:32123]","synonyms":"hsa-mir-518a-2,MIRN518A2,MIRN518A-2","biotype":"miRNA","ncbi_id":"574491","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53739333,"end":53739419,"strand":1,"description":"microRNA 518a-2 [Source:HGNC Symbol;Acc:HGNC:32123]"}, {"versioned_ensembl_gene_id":"ENSG00000277563.1","gene_symbol":"AC063961.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":24255246,"end":24255333,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000265056.1","gene_symbol":"MIR548S","gene_name":"microRNA 548s [Source:HGNC Symbol;Acc:HGNC:38354]","synonyms":"hsa-mir-548s","biotype":"miRNA","ncbi_id":"100422862","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11767444,"end":11767525,"strand":1,"description":"microRNA 548s [Source:HGNC Symbol;Acc:HGNC:38354]"}, {"versioned_ensembl_gene_id":"ENSG00000222808.1","gene_symbol":"RNU4-47P","gene_name":"RNA, U4 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46983]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479579","summary":null,"start":77152561,"end":77152674,"strand":-1,"description":"RNA, U4 small nuclear 47, pseudogene [Source:HGNC Symbol;Acc:HGNC:46983]"}, {"versioned_ensembl_gene_id":"ENSG00000265674.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"ACA48,SNORA48A","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30125305,"end":30125466,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000274459.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68575858,"end":68576136,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000266139.2","gene_symbol":"MIR4435-2","gene_name":"microRNA 4435-2 [Source:HGNC Symbol;Acc:HGNC:41837]","synonyms":"hsa-mir-4435-2","biotype":"miRNA","ncbi_id":"100616341","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111321013,"end":111321086,"strand":-1,"description":"microRNA 4435-2 [Source:HGNC Symbol;Acc:HGNC:41837]"}, {"versioned_ensembl_gene_id":"ENSG00000240823.3","gene_symbol":"RN7SL23P","gene_name":"RNA, 7SL, cytoplasmic 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:46039]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480482","summary":null,"start":61444149,"end":61444423,"strand":1,"description":"RNA, 7SL, cytoplasmic 23, pseudogene [Source:HGNC Symbol;Acc:HGNC:46039]"}, {"versioned_ensembl_gene_id":"ENSG00000202242.1","gene_symbol":"RNU6-1276P","gene_name":"RNA, U6 small nuclear 1276, pseudogene [Source:HGNC Symbol;Acc:HGNC:48239]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481583","summary":null,"start":27773645,"end":27773748,"strand":1,"description":"RNA, U6 small nuclear 1276, pseudogene [Source:HGNC Symbol;Acc:HGNC:48239]"}, {"versioned_ensembl_gene_id":"ENSG00000277590.1","gene_symbol":"MIR7845","gene_name":"microRNA 7845 [Source:HGNC Symbol;Acc:HGNC:50267]","synonyms":"hsa-mir-7845","biotype":"miRNA","ncbi_id":"102465835","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":207166400,"end":207166498,"strand":1,"description":"microRNA 7845 [Source:HGNC Symbol;Acc:HGNC:50267]"}, {"versioned_ensembl_gene_id":"ENSG00000263410.2","gene_symbol":"RN7SL460P","gene_name":"RNA, 7SL, cytoplasmic 460, pseudogene [Source:HGNC Symbol;Acc:HGNC:46476]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481048","summary":null,"start":77885377,"end":77885634,"strand":1,"description":"RNA, 7SL, cytoplasmic 460, pseudogene [Source:HGNC Symbol;Acc:HGNC:46476]"}, {"versioned_ensembl_gene_id":"ENSG00000278242.1","gene_symbol":"RN7SL725P","gene_name":"RNA, 7SL, cytoplasmic 725, pseudogene [Source:HGNC Symbol;Acc:HGNC:46741]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481120","summary":null,"start":25458926,"end":25459184,"strand":1,"description":"RNA, 7SL, cytoplasmic 725, pseudogene [Source:HGNC Symbol;Acc:HGNC:46741]"}, {"versioned_ensembl_gene_id":"ENSG00000207635.1","gene_symbol":"MIR499A","gene_name":"microRNA 499a [Source:HGNC Symbol;Acc:HGNC:32133]","synonyms":"MIRN499,MIR499,hsa-mir-499","biotype":"miRNA","ncbi_id":"574501","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34990376,"end":34990497,"strand":1,"description":"microRNA 499a [Source:HGNC Symbol;Acc:HGNC:32133]"}, {"versioned_ensembl_gene_id":"ENSG00000276183.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":18418526,"end":18418632,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000252198.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":58441844,"end":58441992,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207863.1","gene_symbol":"MIR125B2","gene_name":"microRNA 125b-2 [Source:HGNC Symbol;Acc:HGNC:31507]","synonyms":"MIRN125B2,hsa-mir-125b-2","biotype":"miRNA","ncbi_id":"406912","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16590237,"end":16590325,"strand":1,"description":"microRNA 125b-2 [Source:HGNC Symbol;Acc:HGNC:31507]"}, {"versioned_ensembl_gene_id":"ENSG00000207411.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43620878,"end":43620984,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276696.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56634038,"end":56634167,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252965.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":125528244,"end":125528349,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252057.2","gene_symbol":"RNU7-174P","gene_name":"RNA, U7 small nuclear 174 pseudogene [Source:HGNC Symbol;Acc:HGNC:45708]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480829","summary":null,"start":80560567,"end":80560625,"strand":1,"description":"RNA, U7 small nuclear 174 pseudogene [Source:HGNC Symbol;Acc:HGNC:45708]"}, {"versioned_ensembl_gene_id":"ENSG00000284251.1","gene_symbol":"MIR711","gene_name":"microRNA 711 [Source:HGNC Symbol;Acc:HGNC:37316]","synonyms":"hsa-mir-711","biotype":"miRNA","ncbi_id":"100313843","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48578902,"end":48578977,"strand":-1,"description":"microRNA 711 [Source:HGNC Symbol;Acc:HGNC:37316]"}, {"versioned_ensembl_gene_id":"ENSG00000223015.1","gene_symbol":"RNU6-1135P","gene_name":"RNA, U6 small nuclear 1135, pseudogene [Source:HGNC Symbol;Acc:HGNC:48098]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481538","summary":null,"start":87606783,"end":87606885,"strand":1,"description":"RNA, U6 small nuclear 1135, pseudogene [Source:HGNC Symbol;Acc:HGNC:48098]"}, {"versioned_ensembl_gene_id":"ENSG00000275670.1","gene_symbol":"MIR8076","gene_name":"microRNA 8076 [Source:HGNC Symbol;Acc:HGNC:49997]","synonyms":"hsa-mir-8076","biotype":"miRNA","ncbi_id":"102466253","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113432118,"end":113432200,"strand":-1,"description":"microRNA 8076 [Source:HGNC Symbol;Acc:HGNC:49997]"}, {"versioned_ensembl_gene_id":"ENSG00000263932.1","gene_symbol":"MIR4448","gene_name":"microRNA 4448 [Source:HGNC Symbol;Acc:HGNC:41604]","synonyms":"hsa-mir-4448","biotype":"miRNA","ncbi_id":"100616127","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":183886800,"end":183886885,"strand":1,"description":"microRNA 4448 [Source:HGNC Symbol;Acc:HGNC:41604]"}, {"versioned_ensembl_gene_id":"ENSG00000263746.1","gene_symbol":"MIR4277","gene_name":"microRNA 4277 [Source:HGNC Symbol;Acc:HGNC:38367]","synonyms":"hsa-mir-4277","biotype":"miRNA","ncbi_id":"100422966","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1708785,"end":1708868,"strand":-1,"description":"microRNA 4277 [Source:HGNC Symbol;Acc:HGNC:38367]"}, {"versioned_ensembl_gene_id":"ENSG00000265304.1","gene_symbol":"MIR3650","gene_name":"microRNA 3650 [Source:HGNC Symbol;Acc:HGNC:38981]","synonyms":"hsa-mir-3650","biotype":"miRNA","ncbi_id":"100500824","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38557502,"end":38557561,"strand":-1,"description":"microRNA 3650 [Source:HGNC Symbol;Acc:HGNC:38981]"}, {"versioned_ensembl_gene_id":"ENSG00000264099.1","gene_symbol":"MIR4803","gene_name":"microRNA 4803 [Source:HGNC Symbol;Acc:HGNC:41568]","synonyms":"hsa-mir-4803","biotype":"miRNA","ncbi_id":"100616377","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":72169467,"end":72169540,"strand":1,"description":"microRNA 4803 [Source:HGNC Symbol;Acc:HGNC:41568]"}, {"versioned_ensembl_gene_id":"ENSG00000263963.1","gene_symbol":"MIR4461","gene_name":"microRNA 4461 [Source:HGNC Symbol;Acc:HGNC:41656]","synonyms":"hsa-mir-4461","biotype":"miRNA","ncbi_id":"100616209","summary":"This record was withdrawn by miRBase.","start":134928039,"end":134928112,"strand":1,"description":"microRNA 4461 [Source:HGNC Symbol;Acc:HGNC:41656]"}, {"versioned_ensembl_gene_id":"ENSG00000223174.1","gene_symbol":"RN7SKP17","gene_name":"RNA, 7SK small nuclear pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:45741]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479102","summary":null,"start":76890263,"end":76890613,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:45741]"}, {"versioned_ensembl_gene_id":"ENSG00000277062.1","gene_symbol":"RN7SL88P","gene_name":"RNA, 7SL, cytoplasmic 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:46104]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480945","summary":null,"start":96101951,"end":96102249,"strand":-1,"description":"RNA, 7SL, cytoplasmic 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:46104]"}, {"versioned_ensembl_gene_id":"ENSG00000222240.1","gene_symbol":"RN7SKP156","gene_name":"RNA, 7SK small nuclear pseudogene 156 [Source:HGNC Symbol;Acc:HGNC:45880]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480882","summary":null,"start":188155839,"end":188156180,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 156 [Source:HGNC Symbol;Acc:HGNC:45880]"}, {"versioned_ensembl_gene_id":"ENSG00000263762.1","gene_symbol":"MIR4286","gene_name":"microRNA 4286 [Source:HGNC Symbol;Acc:HGNC:38186]","synonyms":"hsa-mir-4286","biotype":"miRNA","ncbi_id":"100422982","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10666978,"end":10667070,"strand":1,"description":"microRNA 4286 [Source:HGNC Symbol;Acc:HGNC:38186]"}, {"versioned_ensembl_gene_id":"ENSG00000223152.1","gene_symbol":"RNU4-88P","gene_name":"RNA, U4 small nuclear 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:47024]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479599","summary":null,"start":66094461,"end":66094546,"strand":-1,"description":"RNA, U4 small nuclear 88, pseudogene [Source:HGNC Symbol;Acc:HGNC:47024]"}, {"versioned_ensembl_gene_id":"ENSG00000206854.1","gene_symbol":"RNY3P5","gene_name":"RNA, Ro-associated Y3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42489]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873809","summary":null,"start":60789560,"end":60789661,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42489]"}, {"versioned_ensembl_gene_id":"ENSG00000222162.1","gene_symbol":"RN7SKP151","gene_name":"RNA, 7SK small nuclear pseudogene 151 [Source:HGNC Symbol;Acc:HGNC:45875]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479162","summary":null,"start":13353208,"end":13353523,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 151 [Source:HGNC Symbol;Acc:HGNC:45875]"}, {"versioned_ensembl_gene_id":"ENSG00000277713.1","gene_symbol":"MIR6856","gene_name":"microRNA 6856 [Source:HGNC Symbol;Acc:HGNC:50242]","synonyms":"hsa-mir-6856","biotype":"miRNA","ncbi_id":"102465515","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":130626297,"end":130626363,"strand":1,"description":"microRNA 6856 [Source:HGNC Symbol;Acc:HGNC:50242]"}, {"versioned_ensembl_gene_id":"ENSG00000252012.1","gene_symbol":"RNA5SP521","gene_name":"RNA, 5S ribosomal pseudogene 521 [Source:HGNC Symbol;Acc:HGNC:43421]","synonyms":"RN5S521","biotype":"rRNA","ncbi_id":"106479018","summary":null,"start":17559774,"end":17559889,"strand":1,"description":"RNA, 5S ribosomal pseudogene 521 [Source:HGNC Symbol;Acc:HGNC:43421]"}, {"versioned_ensembl_gene_id":"ENSG00000264767.2","gene_symbol":"RN7SL237P","gene_name":"RNA, 7SL, cytoplasmic 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:46253]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479308","summary":null,"start":38098414,"end":38098700,"strand":-1,"description":"RNA, 7SL, cytoplasmic 237, pseudogene [Source:HGNC Symbol;Acc:HGNC:46253]"}, {"versioned_ensembl_gene_id":"ENSG00000277120.5","gene_symbol":"MIR6089","gene_name":"microRNA 6089 [Source:HGNC Symbol;Acc:HGNC:50179]","synonyms":"MIR6089-2,MIR6089-1,hsa-mir-6089-1","biotype":"miRNA","ncbi_id":"102464837","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2609191,"end":2609254,"strand":1,"description":"microRNA 6089 [Source:HGNC Symbol;Acc:HGNC:50179]"}, {"versioned_ensembl_gene_id":"ENSG00000207021.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":81573490,"end":81573602,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212421.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":87260450,"end":87260585,"strand":1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000252250.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":69334600,"end":69334692,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223158.1","gene_symbol":"RNY1P3","gene_name":"RNA, Ro-associated Y1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42480]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873803","summary":null,"start":25950704,"end":25950821,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:42480]"}, {"versioned_ensembl_gene_id":"ENSG00000252642.1","gene_symbol":"RNA5SP137","gene_name":"RNA, 5S ribosomal pseudogene 137 [Source:HGNC Symbol;Acc:HGNC:43037]","synonyms":"RN5S137","biotype":"rRNA","ncbi_id":"100873405","summary":null,"start":125058304,"end":125058438,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 137 [Source:HGNC Symbol;Acc:HGNC:43037]"}, {"versioned_ensembl_gene_id":"ENSG00000266328.3","gene_symbol":"MIR4536-1","gene_name":"microRNA 4536-1 [Source:HGNC Symbol;Acc:HGNC:41730]","synonyms":"MIR4536,hsa-mir-4536","biotype":"miRNA","ncbi_id":"100616155","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55451495,"end":55451582,"strand":1,"description":"microRNA 4536-1 [Source:HGNC Symbol;Acc:HGNC:41730]"}, {"versioned_ensembl_gene_id":"ENSG00000200049.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":143309466,"end":143309566,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212594.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":103592112,"end":103592243,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000251703.1","gene_symbol":"RNU6-998P","gene_name":"RNA, U6 small nuclear 998, pseudogene [Source:HGNC 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Box H/ACA snoRNAs, such as SNORA74B, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":173020728,"end":173020928,"strand":1,"description":"small nucleolar RNA, H/ACA box 74B [Source:HGNC Symbol;Acc:HGNC:32660]"}, {"versioned_ensembl_gene_id":"ENSG00000251792.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50086982,"end":50087083,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212158.1","gene_symbol":"SNORD66","gene_name":"small nucleolar RNA, C/D box 66 [Source:HGNC Symbol;Acc:HGNC:32727]","synonyms":"HBII-142","biotype":"snoRNA","ncbi_id":"692107","summary":null,"start":184325696,"end":184325771,"strand":1,"description":"small nucleolar RNA, C/D box 66 [Source:HGNC Symbol;Acc:HGNC:32727]"}, {"versioned_ensembl_gene_id":"ENSG00000277717.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":86481028,"end":86481130,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000199977.1","gene_symbol":"SNORA73","gene_name":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":21817624,"end":21817828,"strand":1,"description":"Small nucleolar RNA SNORA73 family [Source:RFAM;Acc:RF00045]"}, {"versioned_ensembl_gene_id":"ENSG00000201959.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":77041647,"end":77041748,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277667.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000212625.1","gene_symbol":"RNA5SP397","gene_name":"RNA, 5S ribosomal pseudogene 397 [Source:HGNC Symbol;Acc:HGNC:43297]","synonyms":"RN5S397","biotype":"rRNA","ncbi_id":"100873650","summary":null,"start":60736769,"end":60736886,"strand":1,"description":"RNA, 5S ribosomal pseudogene 397 [Source:HGNC Symbol;Acc:HGNC:43297]"}, {"versioned_ensembl_gene_id":"ENSG00000222455.1","gene_symbol":"RNA5SP296","gene_name":"RNA, 5S ribosomal pseudogene 296 [Source:HGNC Symbol;Acc:HGNC:43196]","synonyms":"RN5S296","biotype":"rRNA","ncbi_id":"100873549","summary":null,"start":127841112,"end":127841222,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 296 [Source:HGNC Symbol;Acc:HGNC:43196]"}, {"versioned_ensembl_gene_id":"ENSG00000201273.1","gene_symbol":"RNU6-776P","gene_name":"RNA, U6 small nuclear 776, pseudogene [Source:HGNC Symbol;Acc:HGNC:47739]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480608","summary":null,"start":22010985,"end":22011088,"strand":1,"description":"RNA, U6 small nuclear 776, pseudogene [Source:HGNC Symbol;Acc:HGNC:47739]"}, {"versioned_ensembl_gene_id":"ENSG00000207276.1","gene_symbol":"RNU6-1160P","gene_name":"RNA, U6 small nuclear 1160, pseudogene [Source:HGNC Symbol;Acc:HGNC:48123]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481546","summary":null,"start":96256216,"end":96256319,"strand":-1,"description":"RNA, U6 small nuclear 1160, pseudogene [Source:HGNC Symbol;Acc:HGNC:48123]"}, {"versioned_ensembl_gene_id":"ENSG00000264592.2","gene_symbol":"RN7SL131P","gene_name":"RNA, 7SL, cytoplasmic 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:46147]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480957","summary":null,"start":36191915,"end":36192170,"strand":1,"description":"RNA, 7SL, cytoplasmic 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:46147]"}, {"versioned_ensembl_gene_id":"ENSG00000252326.1","gene_symbol":"SNORD116-25","gene_name":"small nucleolar RNA, C/D box 116-25 [Source:HGNC Symbol;Acc:HGNC:33091]","synonyms":"HBII-85-25","biotype":"snoRNA","ncbi_id":"100033436","summary":null,"start":25097663,"end":25097754,"strand":1,"description":"small nucleolar RNA, C/D box 116-25 [Source:HGNC Symbol;Acc:HGNC:33091]"}, {"versioned_ensembl_gene_id":"ENSG00000274915.1","gene_symbol":"HAR1A","gene_name":"Highly accelerated region 1A/1B [Source:RFAM;Acc:RF00635]","synonyms":"NCRNA00064,LINC00064,HAR1F","biotype":"misc_RNA","ncbi_id":"768096","summary":null,"start":63102142,"end":63102259,"strand":1,"description":"Highly accelerated region 1A/1B [Source:RFAM;Acc:RF00635]"}, {"versioned_ensembl_gene_id":"ENSG00000276714.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":101322477,"end":101322533,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000275266.1","gene_symbol":"H19_1","gene_name":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1996540,"end":1996610,"strand":1,"description":"H19 conserved region 1 [Source:RFAM;Acc:RF01972]"}, {"versioned_ensembl_gene_id":"ENSG00000222791.1","gene_symbol":"RNU6-67P","gene_name":"RNA, U6 small nuclear 67, pseudogene [Source:HGNC Symbol;Acc:HGNC:42557]","synonyms":"RNU6-67","biotype":"snRNA","ncbi_id":"100873771","summary":null,"start":83298071,"end":83298167,"strand":-1,"description":"RNA, U6 small nuclear 67, pseudogene [Source:HGNC Symbol;Acc:HGNC:42557]"}, {"versioned_ensembl_gene_id":"ENSG00000206715.1","gene_symbol":"RNU6-444P","gene_name":"RNA, U6 small nuclear 444, pseudogene [Source:HGNC Symbol;Acc:HGNC:47407]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479762","summary":null,"start":87488445,"end":87488552,"strand":1,"description":"RNA, U6 small nuclear 444, pseudogene [Source:HGNC Symbol;Acc:HGNC:47407]"}, {"versioned_ensembl_gene_id":"ENSG00000275043.1","gene_symbol":"SNORD25","gene_name":"small nucleolar RNA, C/D box 25 [Source:HGNC Symbol;Acc:HGNC:10147]","synonyms":"U25,RNU25","biotype":"snoRNA","ncbi_id":"9303","summary":null,"start":62855564,"end":62855632,"strand":-1,"description":"small nucleolar RNA, C/D box 25 [Source:HGNC Symbol;Acc:HGNC:10147]"}, {"versioned_ensembl_gene_id":"ENSG00000207033.1","gene_symbol":"RNU6-154P","gene_name":"RNA, U6 small nuclear 154, pseudogene [Source:HGNC Symbol;Acc:HGNC:47117]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481878","summary":null,"start":116400848,"end":116400953,"strand":-1,"description":"RNA, U6 small nuclear 154, pseudogene [Source:HGNC Symbol;Acc:HGNC:47117]"}, {"versioned_ensembl_gene_id":"ENSG00000263793.1","gene_symbol":"MIR3115","gene_name":"microRNA 3115 [Source:HGNC Symbol;Acc:HGNC:38371]","synonyms":"hsa-mir-3115","biotype":"miRNA","ncbi_id":"100422866","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23044305,"end":23044372,"strand":1,"description":"microRNA 3115 [Source:HGNC Symbol;Acc:HGNC:38371]"}, {"versioned_ensembl_gene_id":"ENSG00000274975.1","gene_symbol":"MIR6735","gene_name":"microRNA 6735 [Source:HGNC Symbol;Acc:HGNC:50126]","synonyms":"hsa-mir-6735","biotype":"miRNA","ncbi_id":"102465440","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43448539,"end":43448611,"strand":1,"description":"microRNA 6735 [Source:HGNC Symbol;Acc:HGNC:50126]"}, {"versioned_ensembl_gene_id":"ENSG00000263381.1","gene_symbol":"MIR5584","gene_name":"microRNA 5584 [Source:HGNC Symbol;Acc:HGNC:43507]","synonyms":"hsa-mir-5584","biotype":"miRNA","ncbi_id":"100847089","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44545493,"end":44545552,"strand":1,"description":"microRNA 5584 [Source:HGNC Symbol;Acc:HGNC:43507]"}, {"versioned_ensembl_gene_id":"ENSG00000207729.3","gene_symbol":"MIR556","gene_name":"microRNA 556 [Source:HGNC Symbol;Acc:HGNC:32812]","synonyms":"MIRN556,hsa-mir-556","biotype":"miRNA","ncbi_id":"693141","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":162342546,"end":162342640,"strand":1,"description":"microRNA 556 [Source:HGNC Symbol;Acc:HGNC:32812]"}, {"versioned_ensembl_gene_id":"ENSG00000283598.1","gene_symbol":"MIR1295B","gene_name":"microRNA 1295b [Source:HGNC Symbol;Acc:HGNC:43524]","synonyms":"hsa-mir-1295b","biotype":"miRNA","ncbi_id":"100847009","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":171101739,"end":171101798,"strand":1,"description":"microRNA 1295b [Source:HGNC Symbol;Acc:HGNC:43524]"}, {"versioned_ensembl_gene_id":"ENSG00000274734.1","gene_symbol":"ARHGAP11B","gene_name":"Rho GTPase activating protein 11B [Source:NCBI gene;Acc:89839]","synonyms":"B'-T,FAM7B1,B'-T,FAM7B1","biotype":"protein_coding","ncbi_id":"89839","summary":null,"start":30776860,"end":30837039,"strand":1,"description":"Rho GTPase activating protein 11B [Source:NCBI gene;Acc:89839]"}, {"versioned_ensembl_gene_id":"ENSG00000199529.1","gene_symbol":"RNU6-462P","gene_name":"RNA, U6 small nuclear 462, pseudogene [Source:HGNC Symbol;Acc:HGNC:47425]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479770","summary":null,"start":101723876,"end":101723980,"strand":1,"description":"RNA, U6 small nuclear 462, pseudogene [Source:HGNC Symbol;Acc:HGNC:47425]"}, {"versioned_ensembl_gene_id":"ENSG00000265201.1","gene_symbol":"MIR4677","gene_name":"microRNA 4677 [Source:HGNC Symbol;Acc:HGNC:41844]","synonyms":"hsa-mir-4677","biotype":"miRNA","ncbi_id":"100616343","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":243346176,"end":243346255,"strand":1,"description":"microRNA 4677 [Source:HGNC Symbol;Acc:HGNC:41844]"}, {"versioned_ensembl_gene_id":"ENSG00000275746.1","gene_symbol":"KLF13","gene_name":"Kruppel like factor 13 [Source:HGNC Symbol;Acc:HGNC:13672]","synonyms":"BTEB3,RFLAT-1,NSLP1,FKLF-2,BTEB3,RFLAT-1,NSLP1,FKLF-2","biotype":"protein_coding","ncbi_id":"51621","summary":"KLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]","start":31478417,"end":31529455,"strand":1,"description":"Kruppel like factor 13 [Source:HGNC Symbol;Acc:HGNC:13672]"}, {"versioned_ensembl_gene_id":"ENSG00000221273.1","gene_symbol":"MIR1237","gene_name":"microRNA 1237 [Source:HGNC Symbol;Acc:HGNC:33927]","synonyms":"MIRN1237,hsa-mir-1237","biotype":"miRNA","ncbi_id":"100302280","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64368602,"end":64368703,"strand":1,"description":"microRNA 1237 [Source:HGNC Symbol;Acc:HGNC:33927]"}, {"versioned_ensembl_gene_id":"ENSG00000284435.1","gene_symbol":"MIR4691","gene_name":"microRNA 4691 [Source:HGNC Symbol;Acc:HGNC:41796]","synonyms":"hsa-mir-4691","biotype":"miRNA","ncbi_id":"100616403","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68033897,"end":68033981,"strand":1,"description":"microRNA 4691 [Source:HGNC Symbol;Acc:HGNC:41796]"}, {"versioned_ensembl_gene_id":"ENSG00000284020.1","gene_symbol":"MIR4697","gene_name":"microRNA 4697 [Source:HGNC Symbol;Acc:HGNC:41570]","synonyms":"hsa-mir-4697","biotype":"miRNA","ncbi_id":"100616119","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133898504,"end":133898581,"strand":-1,"description":"microRNA 4697 [Source:HGNC Symbol;Acc:HGNC:41570]"}, {"versioned_ensembl_gene_id":"ENSG00000274194.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000283803.1","gene_symbol":"MIR3198-2","gene_name":"microRNA 3198-2 [Source:HGNC Symbol;Acc:HGNC:41766]","synonyms":"hsa-mir-3198-2","biotype":"miRNA","ncbi_id":"100616400","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54231397,"end":54231476,"strand":-1,"description":"microRNA 3198-2 [Source:HGNC Symbol;Acc:HGNC:41766]"}, {"versioned_ensembl_gene_id":"ENSG00000202485.1","gene_symbol":"RNU6-499P","gene_name":"RNA, U6 small nuclear 499, pseudogene [Source:HGNC Symbol;Acc:HGNC:47462]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479787","summary":null,"start":82174547,"end":82174653,"strand":1,"description":"RNA, U6 small nuclear 499, pseudogene [Source:HGNC Symbol;Acc:HGNC:47462]"}, {"versioned_ensembl_gene_id":"ENSG00000252296.2","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":100100084,"end":100100172,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000243911.3","gene_symbol":"RN7SL430P","gene_name":"RNA, 7SL, cytoplasmic 430, pseudogene [Source:HGNC Symbol;Acc:HGNC:46446]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481040","summary":null,"start":112272596,"end":112272837,"strand":-1,"description":"RNA, 7SL, cytoplasmic 430, pseudogene [Source:HGNC Symbol;Acc:HGNC:46446]"}, {"versioned_ensembl_gene_id":"ENSG00000284388.1","gene_symbol":"MIR4496","gene_name":"microRNA 4496 [Source:HGNC Symbol;Acc:HGNC:41569]","synonyms":"hsa-mir-4496","biotype":"miRNA","ncbi_id":"100616240","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":108635810,"end":108635870,"strand":1,"description":"microRNA 4496 [Source:HGNC Symbol;Acc:HGNC:41569]"}, {"versioned_ensembl_gene_id":"ENSG00000283815.1","gene_symbol":"MIR18A","gene_name":"microRNA 18a [Source:HGNC Symbol;Acc:HGNC:31548]","synonyms":"MIRN18A,MIRN18,hsa-mir-18a,hsa-mir-18","biotype":"miRNA","ncbi_id":"406953","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91350751,"end":91350821,"strand":1,"description":"microRNA 18a [Source:HGNC Symbol;Acc:HGNC:31548]"}, {"versioned_ensembl_gene_id":"ENSG00000283888.1","gene_symbol":"MIR1469","gene_name":"microRNA 1469 [Source:HGNC Symbol;Acc:HGNC:35378]","synonyms":"MIRN1469,hsa-mir-1469","biotype":"miRNA","ncbi_id":"100302258","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96333261,"end":96333307,"strand":1,"description":"microRNA 1469 [Source:HGNC Symbol;Acc:HGNC:35378]"}, {"versioned_ensembl_gene_id":"ENSG00000278450.1","gene_symbol":"BX248413.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29064823,"end":29077352,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000266124.1","gene_symbol":"MIR5587","gene_name":"microRNA 5587 [Source:HGNC Symbol;Acc:HGNC:43508]","synonyms":"hsa-mir-5587","biotype":"miRNA","ncbi_id":"100847028","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":535316,"end":535368,"strand":1,"description":"microRNA 5587 [Source:HGNC Symbol;Acc:HGNC:43508]"}, {"versioned_ensembl_gene_id":"ENSG00000272380.1","gene_symbol":"MIR3976","gene_name":"microRNA 3976 [Source:HGNC Symbol;Acc:HGNC:41578]","synonyms":"hsa-mir-3976","biotype":"miRNA","ncbi_id":"100616244","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5840695,"end":5840833,"strand":1,"description":"microRNA 3976 [Source:HGNC Symbol;Acc:HGNC:41578]"}, {"versioned_ensembl_gene_id":"ENSG00000278066.1","gene_symbol":"AC023491.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":26533,"end":27138,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207580.1","gene_symbol":"MIR526B","gene_name":"microRNA 526b [Source:HGNC Symbol;Acc:HGNC:32100]","synonyms":"MIRN526B,hsa-mir-526b","biotype":"miRNA","ncbi_id":"574468","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53694393,"end":53694475,"strand":1,"description":"microRNA 526b [Source:HGNC Symbol;Acc:HGNC:32100]"}, {"versioned_ensembl_gene_id":"ENSG00000281910.1","gene_symbol":"SNORA50A","gene_name":"small nucleolar RNA, H/ACA box 50A [Source:HGNC Symbol;Acc:HGNC:32643]","synonyms":"SNORA50,ACA50,SNORA76A,SNORA50,ACA50,SNORA76A","biotype":"snoRNA","ncbi_id":"677830","summary":null,"start":58559796,"end":58559931,"strand":-1,"description":"small nucleolar RNA, H/ACA box 50A [Source:HGNC Symbol;Acc:HGNC:32643]"}, {"versioned_ensembl_gene_id":"ENSG00000221725.1","gene_symbol":"RNU6ATAC25P","gene_name":"RNA, U6atac small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46924]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480384","summary":null,"start":70852698,"end":70852814,"strand":1,"description":"RNA, U6atac small nuclear 25, pseudogene [Source:HGNC Symbol;Acc:HGNC:46924]"}, {"versioned_ensembl_gene_id":"ENSG00000265420.1","gene_symbol":"MIR4779","gene_name":"microRNA 4779 [Source:HGNC Symbol;Acc:HGNC:41747]","synonyms":"hsa-mir-4779","biotype":"miRNA","ncbi_id":"100616159","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":86193026,"end":86193108,"strand":-1,"description":"microRNA 4779 [Source:HGNC Symbol;Acc:HGNC:41747]"}, {"versioned_ensembl_gene_id":"ENSG00000278363.1","gene_symbol":"TMC4","gene_name":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]","synonyms":null,"biotype":"protein_coding","ncbi_id":"147798","summary":null,"start":54160649,"end":54173691,"strand":-1,"description":"transmembrane channel like 4 [Source:HGNC Symbol;Acc:HGNC:22998]"}, {"versioned_ensembl_gene_id":"ENSG00000277842.1","gene_symbol":"MIR6811","gene_name":"microRNA 6811 [Source:HGNC Symbol;Acc:HGNC:49944]","synonyms":"hsa-mir-6811","biotype":"miRNA","ncbi_id":"102465486","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":237510931,"end":237510988,"strand":1,"description":"microRNA 6811 [Source:HGNC Symbol;Acc:HGNC:49944]"}, {"versioned_ensembl_gene_id":"ENSG00000266071.1","gene_symbol":"MIR3617","gene_name":"microRNA 3617 [Source:HGNC Symbol;Acc:HGNC:38977]","synonyms":"hsa-mir-3617","biotype":"miRNA","ncbi_id":"100500897","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45705102,"end":45705180,"strand":-1,"description":"microRNA 3617 [Source:HGNC Symbol;Acc:HGNC:38977]"}, {"versioned_ensembl_gene_id":"ENSG00000278426.1","gene_symbol":"LENG1","gene_name":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]","synonyms":null,"biotype":"protein_coding","ncbi_id":"79165","summary":null,"start":54156127,"end":54160192,"strand":-1,"description":"leukocyte receptor cluster member 1 [Source:HGNC Symbol;Acc:HGNC:15502]"}, {"versioned_ensembl_gene_id":"ENSG00000284193.1","gene_symbol":"MIR1257","gene_name":"microRNA 1257 [Source:HGNC Symbol;Acc:HGNC:35322]","synonyms":"MIRN1257,hsa-mir-1257","biotype":"miRNA","ncbi_id":"100302168","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61953546,"end":61953662,"strand":-1,"description":"microRNA 1257 [Source:HGNC Symbol;Acc:HGNC:35322]"}, {"versioned_ensembl_gene_id":"ENSG00000207932.1","gene_symbol":"MIR33A","gene_name":"microRNA 33a [Source:HGNC Symbol;Acc:HGNC:31634]","synonyms":"MIRN33A,MIRN33,hsa-mir-33a,hsa-mir-33","biotype":"miRNA","ncbi_id":"407039","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41900944,"end":41901012,"strand":1,"description":"microRNA 33a [Source:HGNC Symbol;Acc:HGNC:31634]"}, {"versioned_ensembl_gene_id":"ENSG00000274889.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000264160.1","gene_symbol":"MIR4762","gene_name":"microRNA 4762 [Source:HGNC Symbol;Acc:HGNC:41603]","synonyms":"hsa-mir-4762","biotype":"miRNA","ncbi_id":"100616253","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":45760524,"end":45760598,"strand":1,"description":"microRNA 4762 [Source:HGNC Symbol;Acc:HGNC:41603]"}, {"versioned_ensembl_gene_id":"ENSG00000251856.1","gene_symbol":"MIR449C","gene_name":"microRNA 449c [Source:HGNC Symbol;Acc:HGNC:37302]","synonyms":"hsa-mir-449c","biotype":"miRNA","ncbi_id":"100313923","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55172262,"end":55172353,"strand":-1,"description":"microRNA 449c [Source:HGNC Symbol;Acc:HGNC:37302]"}, {"versioned_ensembl_gene_id":"ENSG00000274258.1","gene_symbol":"MIR6728","gene_name":"microRNA 6728 [Source:HGNC Symbol;Acc:HGNC:49961]","synonyms":"hsa-mir-6728","biotype":"miRNA","ncbi_id":"102465436","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8866502,"end":8866590,"strand":-1,"description":"microRNA 6728 [Source:HGNC Symbol;Acc:HGNC:49961]"}, {"versioned_ensembl_gene_id":"ENSG00000283717.1","gene_symbol":"MIR6831","gene_name":"microRNA 6831 [Source:HGNC Symbol;Acc:HGNC:49936]","synonyms":"hsa-mir-6831","biotype":"miRNA","ncbi_id":"102465499","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":140563671,"end":140563751,"strand":-1,"description":"microRNA 6831 [Source:HGNC Symbol;Acc:HGNC:49936]"}, {"versioned_ensembl_gene_id":"ENSG00000276835.2","gene_symbol":"MIR6127","gene_name":"microRNA 6127 [Source:HGNC Symbol;Acc:HGNC:50163]","synonyms":"hsa-mir-6127","biotype":"miRNA","ncbi_id":"102466615","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22633258,"end":22633366,"strand":-1,"description":"microRNA 6127 [Source:HGNC Symbol;Acc:HGNC:50163]"}, {"versioned_ensembl_gene_id":"ENSG00000274994.1","gene_symbol":"MIR8056","gene_name":"microRNA 8056 [Source:HGNC Symbol;Acc:HGNC:49948]","synonyms":"hsa-mir-8056","biotype":"miRNA","ncbi_id":"102465862","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":173347455,"end":173347536,"strand":1,"description":"microRNA 8056 [Source:HGNC Symbol;Acc:HGNC:49948]"}, {"versioned_ensembl_gene_id":"ENSG00000284265.1","gene_symbol":"MIR4683","gene_name":"microRNA 4683 [Source:HGNC Symbol;Acc:HGNC:41883]","synonyms":"hsa-mir-4683","biotype":"miRNA","ncbi_id":"100616500","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":35641172,"end":35641252,"strand":-1,"description":"microRNA 4683 [Source:HGNC Symbol;Acc:HGNC:41883]"}, {"versioned_ensembl_gene_id":"ENSG00000283237.1","gene_symbol":"hsa-mir-550a-1","gene_name":"hsa-mir-550a-1 [Source:miRBase;Acc:MI0003600]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":30289794,"end":30289890,"strand":-1,"description":"hsa-mir-550a-1 [Source:miRBase;Acc:MI0003600]"}, {"versioned_ensembl_gene_id":"ENSG00000283704.1","gene_symbol":"MIR3656","gene_name":"microRNA 3656 [Source:HGNC Symbol;Acc:HGNC:38889]","synonyms":"hsa-mir-3656","biotype":"miRNA","ncbi_id":"100500840","summary":"This record was withdrawn by miRBase.","start":119018944,"end":119019012,"strand":1,"description":"microRNA 3656 [Source:HGNC Symbol;Acc:HGNC:38889]"}, {"versioned_ensembl_gene_id":"ENSG00000252659.1","gene_symbol":"RNU6-1088P","gene_name":"RNA, U6 small nuclear 1088, pseudogene [Source:HGNC Symbol;Acc:HGNC:48051]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480044","summary":null,"start":120313238,"end":120313341,"strand":-1,"description":"RNA, U6 small nuclear 1088, pseudogene [Source:HGNC Symbol;Acc:HGNC:48051]"}, {"versioned_ensembl_gene_id":"ENSG00000238366.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6245731,"end":6245831,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283429.1","gene_symbol":"MIR1244-3","gene_name":"microRNA 1244-3 [Source:HGNC Symbol;Acc:HGNC:38390]","synonyms":"hsa-mir-1244-3","biotype":"miRNA","ncbi_id":"100422872","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":9239467,"end":9239551,"strand":-1,"description":"microRNA 1244-3 [Source:HGNC Symbol;Acc:HGNC:38390]"}, {"versioned_ensembl_gene_id":"ENSG00000266525.1","gene_symbol":"MIR4650-1","gene_name":"microRNA 4650-1 [Source:HGNC Symbol;Acc:HGNC:41755]","synonyms":"hsa-mir-4650-1","biotype":"miRNA","ncbi_id":"100616310","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67114322,"end":67114397,"strand":-1,"description":"microRNA 4650-1 [Source:HGNC Symbol;Acc:HGNC:41755]"}, {"versioned_ensembl_gene_id":"ENSG00000208006.1","gene_symbol":"MIR16-1","gene_name":"microRNA 16-1 [Source:HGNC Symbol;Acc:HGNC:31545]","synonyms":"hsa-mir-16-1,MIRN16-1","biotype":"miRNA","ncbi_id":"406950","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50048973,"end":50049061,"strand":-1,"description":"microRNA 16-1 [Source:HGNC Symbol;Acc:HGNC:31545]"}, {"versioned_ensembl_gene_id":"ENSG00000207826.1","gene_symbol":"MIR596","gene_name":"microRNA 596 [Source:HGNC Symbol;Acc:HGNC:32852]","synonyms":"MIRN596,hsa-mir-596","biotype":"miRNA","ncbi_id":"693181","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1817231,"end":1817307,"strand":1,"description":"microRNA 596 [Source:HGNC Symbol;Acc:HGNC:32852]"}, {"versioned_ensembl_gene_id":"ENSG00000263741.1","gene_symbol":"MIR548AS","gene_name":"microRNA 548as [Source:HGNC Symbol;Acc:HGNC:43550]","synonyms":"hsa-mir-548as","biotype":"miRNA","ncbi_id":"100847092","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":92490163,"end":92490220,"strand":1,"description":"microRNA 548as [Source:HGNC Symbol;Acc:HGNC:43550]"}, {"versioned_ensembl_gene_id":"ENSG00000207595.1","gene_symbol":"MIR181A2","gene_name":"microRNA 181a-2 [Source:HGNC Symbol;Acc:HGNC:31549]","synonyms":"MIRN181A2,MIRN181A,hsa-mir-181a","biotype":"miRNA","ncbi_id":"406954","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124692442,"end":124692551,"strand":1,"description":"microRNA 181a-2 [Source:HGNC Symbol;Acc:HGNC:31549]"}, {"versioned_ensembl_gene_id":"ENSG00000274063.1","gene_symbol":"AL662852.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29060593,"end":29073129,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283636.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63168600,"end":63168847,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207209.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":147420199,"end":147420300,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207247.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136934765,"end":136934866,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199422.1","gene_symbol":"VTRNA3-1P","gene_name":"vault RNA 3-1, pseudogene [Source:HGNC Symbol;Acc:HGNC:23027]","synonyms":"VTRNA3P,VAULTRC4,HVG4,hvg-4","biotype":"misc_RNA","ncbi_id":"100144435","summary":null,"start":53462209,"end":53462310,"strand":1,"description":"vault RNA 3-1, pseudogene [Source:HGNC Symbol;Acc:HGNC:23027]"}, {"versioned_ensembl_gene_id":"ENSG00000284585.1","gene_symbol":"MIR4722","gene_name":"microRNA 4722 [Source:HGNC Symbol;Acc:HGNC:41782]","synonyms":"hsa-mir-4722","biotype":"miRNA","ncbi_id":"100616167","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88716278,"end":88716337,"strand":-1,"description":"microRNA 4722 [Source:HGNC Symbol;Acc:HGNC:41782]"}, {"versioned_ensembl_gene_id":"ENSG00000266827.1","gene_symbol":"MIR3689E","gene_name":"microRNA 3689e [Source:HGNC Symbol;Acc:HGNC:41887]","synonyms":"hsa-mir-3689e","biotype":"miRNA","ncbi_id":"100616460","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850570,"end":134850641,"strand":-1,"description":"microRNA 3689e [Source:HGNC Symbol;Acc:HGNC:41887]"}, {"versioned_ensembl_gene_id":"ENSG00000207612.1","gene_symbol":"MIR604","gene_name":"microRNA 604 [Source:HGNC Symbol;Acc:HGNC:32860]","synonyms":"MIRN604,hsa-mir-604","biotype":"miRNA","ncbi_id":"693189","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":29545004,"end":29545097,"strand":-1,"description":"microRNA 604 [Source:HGNC Symbol;Acc:HGNC:32860]"}, {"versioned_ensembl_gene_id":"ENSG00000283805.1","gene_symbol":"MIR636","gene_name":"microRNA 636 [Source:HGNC Symbol;Acc:HGNC:32892]","synonyms":"MIRN636,hsa-mir-636","biotype":"miRNA","ncbi_id":"693221","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":76736450,"end":76736548,"strand":-1,"description":"microRNA 636 [Source:HGNC Symbol;Acc:HGNC:32892]"}, {"versioned_ensembl_gene_id":"ENSG00000221348.1","gene_symbol":"MIR548F5","gene_name":"microRNA 548f-5 [Source:HGNC Symbol;Acc:HGNC:35309]","synonyms":"MIRN548F5,hsa-mir-548f-5","biotype":"miRNA","ncbi_id":"100302239","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32641474,"end":32641559,"strand":-1,"description":"microRNA 548f-5 [Source:HGNC Symbol;Acc:HGNC:35309]"}, {"versioned_ensembl_gene_id":"ENSG00000278529.1","gene_symbol":"MIR8070","gene_name":"microRNA 8070 [Source:HGNC Symbol;Acc:HGNC:50274]","synonyms":"hsa-mir-8070","biotype":"miRNA","ncbi_id":"102465870","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11783135,"end":11783222,"strand":-1,"description":"microRNA 8070 [Source:HGNC Symbol;Acc:HGNC:50274]"}, {"versioned_ensembl_gene_id":"ENSG00000242398.3","gene_symbol":"RN7SL800P","gene_name":"RNA, 7SL, cytoplasmic 800, pseudogene [Source:HGNC Symbol;Acc:HGNC:46816]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479512","summary":null,"start":62005737,"end":62006016,"strand":-1,"description":"RNA, 7SL, cytoplasmic 800, pseudogene [Source:HGNC Symbol;Acc:HGNC:46816]"}, {"versioned_ensembl_gene_id":"ENSG00000206815.1","gene_symbol":"RNU6-483P","gene_name":"RNA, U6 small nuclear 483, pseudogene [Source:HGNC Symbol;Acc:HGNC:47446]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479780","summary":null,"start":57548838,"end":57548945,"strand":1,"description":"RNA, U6 small nuclear 483, pseudogene [Source:HGNC Symbol;Acc:HGNC:47446]"}, {"versioned_ensembl_gene_id":"ENSG00000244357.3","gene_symbol":"RN7SL145P","gene_name":"RNA, 7SL, cytoplasmic 145, pseudogene [Source:HGNC Symbol;Acc:HGNC:46161]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481753","summary":null,"start":45742675,"end":45742970,"strand":1,"description":"RNA, 7SL, cytoplasmic 145, pseudogene [Source:HGNC Symbol;Acc:HGNC:46161]"}, {"versioned_ensembl_gene_id":"ENSG00000207176.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32396050,"end":32396147,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264571.1","gene_symbol":"MIR4529","gene_name":"microRNA 4529 [Source:HGNC Symbol;Acc:HGNC:41703]","synonyms":"hsa-mir-4529","biotype":"miRNA","ncbi_id":"100616290","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55479221,"end":55479298,"strand":1,"description":"microRNA 4529 [Source:HGNC Symbol;Acc:HGNC:41703]"}, {"versioned_ensembl_gene_id":"ENSG00000273874.1","gene_symbol":"MIR6859-2","gene_name":"microRNA 6859-2 [Source:HGNC Symbol;Acc:HGNC:49954]","synonyms":"hsa-mir-6859-2","biotype":"miRNA","ncbi_id":"102465909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":187891,"end":187958,"strand":-1,"description":"microRNA 6859-2 [Source:HGNC Symbol;Acc:HGNC:49954]"}, {"versioned_ensembl_gene_id":"ENSG00000207957.1","gene_symbol":"MIR105-1","gene_name":"microRNA 105-1 [Source:HGNC Symbol;Acc:HGNC:31492]","synonyms":"MIRN105-1,hsa-mir-105-1","biotype":"miRNA","ncbi_id":"406897","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152392219,"end":152392299,"strand":-1,"description":"microRNA 105-1 [Source:HGNC Symbol;Acc:HGNC:31492]"}, {"versioned_ensembl_gene_id":"ENSG00000207562.3","gene_symbol":"MIR34C","gene_name":"microRNA 34c [Source:HGNC Symbol;Acc:HGNC:31637]","synonyms":"MIRN34C,hsa-mir-34c","biotype":"miRNA","ncbi_id":"407042","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111513439,"end":111513515,"strand":1,"description":"microRNA 34c [Source:HGNC Symbol;Acc:HGNC:31637]"}, {"versioned_ensembl_gene_id":"ENSG00000283842.1","gene_symbol":"MIR4751","gene_name":"microRNA 4751 [Source:HGNC Symbol;Acc:HGNC:41819]","synonyms":"hsa-mir-4751","biotype":"miRNA","ncbi_id":"100616483","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49933064,"end":49933137,"strand":1,"description":"microRNA 4751 [Source:HGNC Symbol;Acc:HGNC:41819]"}, {"versioned_ensembl_gene_id":"ENSG00000239942.2","gene_symbol":"RN7SL394P","gene_name":"RNA, 7SL, cytoplasmic 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:46410]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479367","summary":null,"start":67825310,"end":67825600,"strand":-1,"description":"RNA, 7SL, cytoplasmic 394, pseudogene [Source:HGNC Symbol;Acc:HGNC:46410]"}, {"versioned_ensembl_gene_id":"ENSG00000276869.1","gene_symbol":"MIR6729","gene_name":"microRNA 6729 [Source:HGNC Symbol;Acc:HGNC:50103]","synonyms":"hsa-mir-6729","biotype":"miRNA","ncbi_id":"102466982","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12029158,"end":12029222,"strand":1,"description":"microRNA 6729 [Source:HGNC Symbol;Acc:HGNC:50103]"}, {"versioned_ensembl_gene_id":"ENSG00000212533.1","gene_symbol":"SNORA75","gene_name":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]","synonyms":"U23,SNORA75A","biotype":"snoRNA","ncbi_id":"654321","summary":null,"start":31076867,"end":31077016,"strand":-1,"description":"Small nucleolar RNA SNORA75 [Source:RFAM;Acc:RF00072]"}, {"versioned_ensembl_gene_id":"ENSG00000200622.1","gene_symbol":"RNU6-1059P","gene_name":"RNA, U6 small nuclear 1059, pseudogene [Source:HGNC Symbol;Acc:HGNC:48022]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480031","summary":null,"start":95868667,"end":95868764,"strand":-1,"description":"RNA, U6 small nuclear 1059, pseudogene [Source:HGNC Symbol;Acc:HGNC:48022]"}, {"versioned_ensembl_gene_id":"ENSG00000252269.1","gene_symbol":"RNU4ATAC12P","gene_name":"RNA, U4atac small nuclear 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:46898]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481865","summary":null,"start":132995190,"end":132995302,"strand":-1,"description":"RNA, U4atac small nuclear 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:46898]"}, {"versioned_ensembl_gene_id":"ENSG00000284536.1","gene_symbol":"MIR17","gene_name":"microRNA 17 [Source:HGNC Symbol;Acc:HGNC:31547]","synonyms":"MIRN17,hsa-mir-17","biotype":"miRNA","ncbi_id":"406952","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91350605,"end":91350688,"strand":1,"description":"microRNA 17 [Source:HGNC Symbol;Acc:HGNC:31547]"}, {"versioned_ensembl_gene_id":"ENSG00000207549.1","gene_symbol":"MIR521-2","gene_name":"microRNA 521-2 [Source:HGNC Symbol;Acc:HGNC:32113]","synonyms":"MIRN521-2,hsa-mir-521-2","biotype":"miRNA","ncbi_id":"574481","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53716594,"end":53716680,"strand":1,"description":"microRNA 521-2 [Source:HGNC Symbol;Acc:HGNC:32113]"}, {"versioned_ensembl_gene_id":"ENSG00000276733.1","gene_symbol":"MIR7158","gene_name":"microRNA 7158 [Source:HGNC Symbol;Acc:HGNC:49971]","synonyms":"hsa-mir-7158","biotype":"miRNA","ncbi_id":"102465693","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5974662,"end":5974732,"strand":1,"description":"microRNA 7158 [Source:HGNC Symbol;Acc:HGNC:49971]"}, {"versioned_ensembl_gene_id":"ENSG00000264712.3","gene_symbol":"MIR4504","gene_name":"microRNA 4504 [Source:HGNC Symbol;Acc:HGNC:41624]","synonyms":"hsa-mir-4504","biotype":"miRNA","ncbi_id":"100616261","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50299855,"end":50299946,"strand":-1,"description":"microRNA 4504 [Source:HGNC Symbol;Acc:HGNC:41624]"}, {"versioned_ensembl_gene_id":"ENSG00000240723.3","gene_symbol":"RN7SL382P","gene_name":"RNA, 7SL, cytoplasmic 382, pseudogene [Source:HGNC Symbol;Acc:HGNC:46398]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481027","summary":null,"start":139100377,"end":139100658,"strand":1,"description":"RNA, 7SL, cytoplasmic 382, pseudogene [Source:HGNC Symbol;Acc:HGNC:46398]"}, {"versioned_ensembl_gene_id":"ENSG00000207721.1","gene_symbol":"MIR186","gene_name":"microRNA 186 [Source:HGNC Symbol;Acc:HGNC:31557]","synonyms":"MIRN186,hsa-mir-186","biotype":"miRNA","ncbi_id":"406962","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":71067631,"end":71067716,"strand":-1,"description":"microRNA 186 [Source:HGNC Symbol;Acc:HGNC:31557]"}, {"versioned_ensembl_gene_id":"ENSG00000266545.1","gene_symbol":"MIR5701-1","gene_name":"microRNA 5701-1 [Source:HGNC Symbol;Acc:HGNC:43522]","synonyms":"hsa-mir-5701-1","biotype":"miRNA","ncbi_id":"100847060","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20940252,"end":20940333,"strand":1,"description":"microRNA 5701-1 [Source:HGNC Symbol;Acc:HGNC:43522]"}, {"versioned_ensembl_gene_id":"ENSG00000212342.1","gene_symbol":"SNORA12","gene_name":"Small nucleolar RNA SNORA12 [Source:RFAM;Acc:RF00586]","synonyms":"U108","biotype":"snoRNA","ncbi_id":"677800","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":130162972,"end":130163127,"strand":1,"description":"Small nucleolar RNA SNORA12 [Source:RFAM;Acc:RF00586]"}, {"versioned_ensembl_gene_id":"ENSG00000199633.1","gene_symbol":"SNORA63","gene_name":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]","synonyms":"RNE3,E3,RNU107,E3-2,SNORA63A","biotype":"snoRNA","ncbi_id":"6043","summary":null,"start":78091172,"end":78091297,"strand":-1,"description":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]"}, {"versioned_ensembl_gene_id":"ENSG00000263783.1","gene_symbol":"MIR5590","gene_name":"microRNA 5590 [Source:HGNC Symbol;Acc:HGNC:43541]","synonyms":"hsa-mir-5590","biotype":"miRNA","ncbi_id":"100847069","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134857820,"end":134857873,"strand":1,"description":"microRNA 5590 [Source:HGNC Symbol;Acc:HGNC:43541]"}, {"versioned_ensembl_gene_id":"ENSG00000202329.1","gene_symbol":"RNU6-609P","gene_name":"RNA, U6 small nuclear 609, pseudogene [Source:HGNC Symbol;Acc:HGNC:47572]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481906","summary":null,"start":200014689,"end":200014795,"strand":-1,"description":"RNA, U6 small nuclear 609, pseudogene [Source:HGNC Symbol;Acc:HGNC:47572]"}, {"versioned_ensembl_gene_id":"ENSG00000263964.1","gene_symbol":"MIR4509-3","gene_name":"microRNA 4509-3 [Source:HGNC Symbol;Acc:HGNC:41610]","synonyms":"hsa-mir-4509-3","biotype":"miRNA","ncbi_id":"100616382","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28490752,"end":28490845,"strand":-1,"description":"microRNA 4509-3 [Source:HGNC Symbol;Acc:HGNC:41610]"}, {"versioned_ensembl_gene_id":"ENSG00000276081.1","gene_symbol":"MIR7156","gene_name":"microRNA 7156 [Source:HGNC Symbol;Acc:HGNC:50023]","synonyms":"hsa-mir-7156","biotype":"miRNA","ncbi_id":"102466995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77060143,"end":77060202,"strand":1,"description":"microRNA 7156 [Source:HGNC Symbol;Acc:HGNC:50023]"}, {"versioned_ensembl_gene_id":"ENSG00000207611.1","gene_symbol":"MIR149","gene_name":"microRNA 149 [Source:HGNC Symbol;Acc:HGNC:31536]","synonyms":"MIRN149,hsa-mir-149","biotype":"miRNA","ncbi_id":"406941","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":240456001,"end":240456089,"strand":1,"description":"microRNA 149 [Source:HGNC Symbol;Acc:HGNC:31536]"}, {"versioned_ensembl_gene_id":"ENSG00000201010.1","gene_symbol":"RN7SKP224","gene_name":"RNA, 7SK small nuclear pseudogene 224 [Source:HGNC Symbol;Acc:HGNC:45948]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480902","summary":null,"start":48217575,"end":48217899,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 224 [Source:HGNC Symbol;Acc:HGNC:45948]"}, {"versioned_ensembl_gene_id":"ENSG00000207703.1","gene_symbol":"MIR7-2","gene_name":"microRNA 7-2 [Source:HGNC Symbol;Acc:HGNC:31639]","synonyms":"MIRN7-2,hsa-mir-7-2","biotype":"miRNA","ncbi_id":"407044","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88611825,"end":88611934,"strand":1,"description":"microRNA 7-2 [Source:HGNC Symbol;Acc:HGNC:31639]"}, {"versioned_ensembl_gene_id":"ENSG00000264580.1","gene_symbol":"MIR5692B","gene_name":"microRNA 5692b [Source:HGNC Symbol;Acc:HGNC:43535]","synonyms":"hsa-mir-5692b","biotype":"miRNA","ncbi_id":"100847013","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42950928,"end":42951014,"strand":-1,"description":"microRNA 5692b [Source:HGNC Symbol;Acc:HGNC:43535]"}, {"versioned_ensembl_gene_id":"ENSG00000272435.1","gene_symbol":"RNA5SP357","gene_name":"RNA, 5S ribosomal pseudogene 357 [Source:HGNC Symbol;Acc:HGNC:43257]","synonyms":"RN5S357","biotype":"rRNA","ncbi_id":"100873616","summary":null,"start":34205699,"end":34205817,"strand":1,"description":"RNA, 5S ribosomal pseudogene 357 [Source:HGNC Symbol;Acc:HGNC:43257]"}, {"versioned_ensembl_gene_id":"ENSG00000212384.1","gene_symbol":"SNORD113-2","gene_name":"small nucleolar RNA, C/D box 113-2 [Source:HGNC Symbol;Acc:HGNC:32981]","synonyms":"14q(I-2)","biotype":"snoRNA","ncbi_id":"767562","summary":null,"start":100927342,"end":100927413,"strand":1,"description":"small nucleolar RNA, C/D box 113-2 [Source:HGNC Symbol;Acc:HGNC:32981]"}, {"versioned_ensembl_gene_id":"ENSG00000277681.1","gene_symbol":"MIR6739","gene_name":"microRNA 6739 [Source:HGNC Symbol;Acc:HGNC:50165]","synonyms":"hsa-mir-6739","biotype":"miRNA","ncbi_id":"102466724","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":201863373,"end":201863447,"strand":1,"description":"microRNA 6739 [Source:HGNC Symbol;Acc:HGNC:50165]"}, {"versioned_ensembl_gene_id":"ENSG00000207561.1","gene_symbol":"MIR635","gene_name":"microRNA 635 [Source:HGNC Symbol;Acc:HGNC:32891]","synonyms":"MIRN635,hsa-mir-635","biotype":"miRNA","ncbi_id":"693220","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68424451,"end":68424548,"strand":-1,"description":"microRNA 635 [Source:HGNC Symbol;Acc:HGNC:32891]"}, {"versioned_ensembl_gene_id":"ENSG00000275810.1","gene_symbol":"MIR8082","gene_name":"microRNA 8082 [Source:HGNC Symbol;Acc:HGNC:50111]","synonyms":"hsa-mir-8082","biotype":"miRNA","ncbi_id":"102465878","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113152282,"end":113152362,"strand":1,"description":"microRNA 8082 [Source:HGNC Symbol;Acc:HGNC:50111]"}, {"versioned_ensembl_gene_id":"ENSG00000199424.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":136571705,"end":136571815,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264678.1","gene_symbol":"MIR3140","gene_name":"microRNA 3140 [Source:HGNC Symbol;Acc:HGNC:38183]","synonyms":"hsa-mir-3140","biotype":"miRNA","ncbi_id":"100422896","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152489327,"end":152489416,"strand":-1,"description":"microRNA 3140 [Source:HGNC Symbol;Acc:HGNC:38183]"}, {"versioned_ensembl_gene_id":"ENSG00000265561.2","gene_symbol":"MIR1268B","gene_name":"microRNA 1268b [Source:HGNC Symbol;Acc:HGNC:41581]","synonyms":"hsa-mir-1268b","biotype":"miRNA","ncbi_id":"100616121","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80098828,"end":80098877,"strand":1,"description":"microRNA 1268b [Source:HGNC Symbol;Acc:HGNC:41581]"}, {"versioned_ensembl_gene_id":"ENSG00000222071.1","gene_symbol":"MIR1915","gene_name":"microRNA 1915 [Source:HGNC Symbol;Acc:HGNC:35399]","synonyms":"MIRN1915,hsa-mir-1915","biotype":"miRNA","ncbi_id":"100302129","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21496562,"end":21496641,"strand":-1,"description":"microRNA 1915 [Source:HGNC Symbol;Acc:HGNC:35399]"}, {"versioned_ensembl_gene_id":"ENSG00000240205.3","gene_symbol":"RN7SL865P","gene_name":"RNA, 7SL, cytoplasmic 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:46881]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481154","summary":null,"start":115717725,"end":115718013,"strand":1,"description":"RNA, 7SL, cytoplasmic 865, pseudogene [Source:HGNC Symbol;Acc:HGNC:46881]"}, {"versioned_ensembl_gene_id":"ENSG00000239075.1","gene_symbol":"RNU6-274P","gene_name":"RNA, U6 small nuclear 274, pseudogene [Source:HGNC Symbol;Acc:HGNC:47237]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479688","summary":null,"start":89754620,"end":89754726,"strand":-1,"description":"RNA, U6 small nuclear 274, pseudogene [Source:HGNC Symbol;Acc:HGNC:47237]"}, {"versioned_ensembl_gene_id":"ENSG00000241943.2","gene_symbol":"RN7SL188P","gene_name":"RNA, 7SL, cytoplasmic 188, pseudogene [Source:HGNC Symbol;Acc:HGNC:46204]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479290","summary":null,"start":16576851,"end":16577135,"strand":1,"description":"RNA, 7SL, cytoplasmic 188, pseudogene [Source:HGNC Symbol;Acc:HGNC:46204]"}, {"versioned_ensembl_gene_id":"ENSG00000266721.1","gene_symbol":"MIR5695","gene_name":"microRNA 5695 [Source:HGNC Symbol;Acc:HGNC:43548]","synonyms":"hsa-mir-5695","biotype":"miRNA","ncbi_id":"100847016","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12920320,"end":12920404,"strand":1,"description":"microRNA 5695 [Source:HGNC Symbol;Acc:HGNC:43548]"}, {"versioned_ensembl_gene_id":"ENSG00000263831.1","gene_symbol":"MIR378E","gene_name":"microRNA 378e [Source:HGNC Symbol;Acc:HGNC:41671]","synonyms":"hsa-mir-378e","biotype":"miRNA","ncbi_id":"100616498","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":170028488,"end":170028566,"strand":1,"description":"microRNA 378e [Source:HGNC Symbol;Acc:HGNC:41671]"}, {"versioned_ensembl_gene_id":"ENSG00000207616.1","gene_symbol":"MIR515-1","gene_name":"microRNA 515-1 [Source:HGNC Symbol;Acc:HGNC:32094]","synonyms":"MIRN515-1,hsa-mir-515-1","biotype":"miRNA","ncbi_id":"574462","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53679003,"end":53679085,"strand":1,"description":"microRNA 515-1 [Source:HGNC Symbol;Acc:HGNC:32094]"}, {"versioned_ensembl_gene_id":"ENSG00000251960.1","gene_symbol":"RNU6-559P","gene_name":"RNA, U6 small nuclear 559, pseudogene [Source:HGNC Symbol;Acc:HGNC:47522]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481771","summary":null,"start":15143289,"end":15143386,"strand":1,"description":"RNA, U6 small nuclear 559, pseudogene [Source:HGNC Symbol;Acc:HGNC:47522]"}, {"versioned_ensembl_gene_id":"ENSG00000266318.1","gene_symbol":"MIR5692A1","gene_name":"microRNA 5692a-1 [Source:HGNC Symbol;Acc:HGNC:43533]","synonyms":"hsa-mir-5692a-1","biotype":"miRNA","ncbi_id":"100847066","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97963658,"end":97963726,"strand":1,"description":"microRNA 5692a-1 [Source:HGNC Symbol;Acc:HGNC:43533]"}, {"versioned_ensembl_gene_id":"ENSG00000221594.1","gene_symbol":"MIR548F1","gene_name":"microRNA 548f-1 [Source:HGNC Symbol;Acc:HGNC:35305]","synonyms":"hsa-mir-548f-1,MIRN548F1","biotype":"miRNA","ncbi_id":"100302192","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54607874,"end":54607957,"strand":-1,"description":"microRNA 548f-1 [Source:HGNC Symbol;Acc:HGNC:35305]"}, {"versioned_ensembl_gene_id":"ENSG00000207594.1","gene_symbol":"MIR520A","gene_name":"microRNA 520a [Source:HGNC Symbol;Acc:HGNC:32099]","synonyms":"MIRN520A,hsa-mir-520a","biotype":"miRNA","ncbi_id":"574467","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53690881,"end":53690965,"strand":1,"description":"microRNA 520a [Source:HGNC Symbol;Acc:HGNC:32099]"}, {"versioned_ensembl_gene_id":"ENSG00000243346.3","gene_symbol":"RN7SL601P","gene_name":"RNA, 7SL, cytoplasmic 601, pseudogene [Source:HGNC Symbol;Acc:HGNC:46617]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480520","summary":null,"start":11157455,"end":11157747,"strand":1,"description":"RNA, 7SL, cytoplasmic 601, pseudogene [Source:HGNC Symbol;Acc:HGNC:46617]"}, {"versioned_ensembl_gene_id":"ENSG00000221574.1","gene_symbol":"RNU6ATAC33P","gene_name":"RNA, U6atac small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:46932]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481170","summary":null,"start":10399192,"end":10399317,"strand":-1,"description":"RNA, U6atac small nuclear 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:46932]"}, {"versioned_ensembl_gene_id":"ENSG00000283821.1","gene_symbol":"MIR6875","gene_name":"microRNA 6875 [Source:HGNC Symbol;Acc:HGNC:50015]","synonyms":"hsa-mir-6875","biotype":"miRNA","ncbi_id":"102466755","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100868036,"end":100868107,"strand":1,"description":"microRNA 6875 [Source:HGNC Symbol;Acc:HGNC:50015]"}, {"versioned_ensembl_gene_id":"ENSG00000238987.1","gene_symbol":"RNU7-133P","gene_name":"RNA, U7 small nuclear 133 pseudogene [Source:HGNC Symbol;Acc:HGNC:45667]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479075","summary":null,"start":14156462,"end":14156523,"strand":1,"description":"RNA, U7 small nuclear 133 pseudogene [Source:HGNC Symbol;Acc:HGNC:45667]"}, {"versioned_ensembl_gene_id":"ENSG00000207551.1","gene_symbol":"MIR608","gene_name":"microRNA 608 [Source:HGNC Symbol;Acc:HGNC:32864]","synonyms":"MIRN608,hsa-mir-608","biotype":"miRNA","ncbi_id":"693193","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100974985,"end":100975084,"strand":1,"description":"microRNA 608 [Source:HGNC Symbol;Acc:HGNC:32864]"}, {"versioned_ensembl_gene_id":"ENSG00000265429.3","gene_symbol":"MIR4782","gene_name":"microRNA 4782 [Source:HGNC Symbol;Acc:HGNC:41635]","synonyms":"hsa-mir-4782","biotype":"miRNA","ncbi_id":"100616208","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113721290,"end":113721368,"strand":-1,"description":"microRNA 4782 [Source:HGNC Symbol;Acc:HGNC:41635]"}, {"versioned_ensembl_gene_id":"ENSG00000221305.1","gene_symbol":"MIR548I3","gene_name":"microRNA 548i-3 [Source:HGNC Symbol;Acc:HGNC:35354]","synonyms":"MIRN548I3,hsa-mir-548i-3","biotype":"miRNA","ncbi_id":"100302186","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8088941,"end":8089089,"strand":-1,"description":"microRNA 548i-3 [Source:HGNC Symbol;Acc:HGNC:35354]"}, {"versioned_ensembl_gene_id":"ENSG00000252505.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":33540040,"end":33540137,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000275141.1","gene_symbol":"MIR6888","gene_name":"microRNA 6888 [Source:HGNC Symbol;Acc:HGNC:50071]","synonyms":"hsa-mir-6888","biotype":"miRNA","ncbi_id":"102465535","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":159186835,"end":159186901,"strand":1,"description":"microRNA 6888 [Source:HGNC Symbol;Acc:HGNC:50071]"}, {"versioned_ensembl_gene_id":"ENSG00000207995.1","gene_symbol":"MIR325","gene_name":"microRNA 325 [Source:HGNC Symbol;Acc:HGNC:31768]","synonyms":"MIRN325,hsa-mir-325","biotype":"miRNA","ncbi_id":"442899","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":77005404,"end":77005501,"strand":-1,"description":"microRNA 325 [Source:HGNC Symbol;Acc:HGNC:31768]"}, {"versioned_ensembl_gene_id":"ENSG00000276120.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30242579,"end":30242815,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222972.1","gene_symbol":"RNU6-651P","gene_name":"RNA, U6 small nuclear 651, pseudogene [Source:HGNC Symbol;Acc:HGNC:47614]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479855","summary":null,"start":201646716,"end":201646820,"strand":1,"description":"RNA, U6 small nuclear 651, pseudogene [Source:HGNC Symbol;Acc:HGNC:47614]"}, {"versioned_ensembl_gene_id":"ENSG00000251862.2","gene_symbol":"MIR1343","gene_name":"microRNA 1343 [Source:HGNC Symbol;Acc:HGNC:41902]","synonyms":"hsa-mir-1343","biotype":"miRNA","ncbi_id":"100616437","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34941837,"end":34941920,"strand":1,"description":"microRNA 1343 [Source:HGNC Symbol;Acc:HGNC:41902]"}, {"versioned_ensembl_gene_id":"ENSG00000263967.1","gene_symbol":"MIR4290","gene_name":"microRNA 4290 [Source:HGNC Symbol;Acc:HGNC:38360]","synonyms":"hsa-mir-4290","biotype":"miRNA","ncbi_id":"100422963","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90023441,"end":90023535,"strand":-1,"description":"microRNA 4290 [Source:HGNC Symbol;Acc:HGNC:38360]"}, {"versioned_ensembl_gene_id":"ENSG00000199313.1","gene_symbol":"RNU4-82P","gene_name":"RNA, U4 small nuclear 82, pseudogene [Source:HGNC Symbol;Acc:HGNC:47018]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481198","summary":null,"start":124887410,"end":124887549,"strand":-1,"description":"RNA, U4 small nuclear 82, pseudogene [Source:HGNC Symbol;Acc:HGNC:47018]"}, {"versioned_ensembl_gene_id":"ENSG00000206990.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":165662585,"end":165662687,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264539.1","gene_symbol":"MIR548AR","gene_name":"microRNA 548ar [Source:HGNC Symbol;Acc:HGNC:43455]","synonyms":"hsa-mir-548ar","biotype":"miRNA","ncbi_id":"100847035","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114244505,"end":114244561,"strand":1,"description":"microRNA 548ar [Source:HGNC Symbol;Acc:HGNC:43455]"}, {"versioned_ensembl_gene_id":"ENSG00000274115.1","gene_symbol":"MIR6081","gene_name":"microRNA 6081 [Source:HGNC Symbol;Acc:HGNC:50151]","synonyms":"hsa-mir-6081","biotype":"miRNA","ncbi_id":"102466518","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95065350,"end":95065446,"strand":1,"description":"microRNA 6081 [Source:HGNC Symbol;Acc:HGNC:50151]"}, {"versioned_ensembl_gene_id":"ENSG00000222788.1","gene_symbol":"RNU2-38P","gene_name":"RNA, U2 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48531]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481646","summary":null,"start":148939739,"end":148939817,"strand":-1,"description":"RNA, U2 small nuclear 38, pseudogene [Source:HGNC Symbol;Acc:HGNC:48531]"}, {"versioned_ensembl_gene_id":"ENSG00000222440.1","gene_symbol":"RNU2-26P","gene_name":"RNA, U2 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:48519]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480414","summary":null,"start":91798093,"end":91798283,"strand":1,"description":"RNA, U2 small nuclear 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:48519]"}, {"versioned_ensembl_gene_id":"ENSG00000207867.1","gene_symbol":"MIR514A3","gene_name":"microRNA 514a-3 [Source:HGNC Symbol;Acc:HGNC:32150]","synonyms":"MIRN514-3,MIR514-3,hsa-mir-514-3","biotype":"miRNA","ncbi_id":"574518","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147284641,"end":147284728,"strand":-1,"description":"microRNA 514a-3 [Source:HGNC Symbol;Acc:HGNC:32150]"}, {"versioned_ensembl_gene_id":"ENSG00000221745.3","gene_symbol":"MIR1197","gene_name":"microRNA 1197 [Source:HGNC Symbol;Acc:HGNC:35376]","synonyms":"MIRN1197,hsa-mir-1197","biotype":"miRNA","ncbi_id":"100302250","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101025564,"end":101025651,"strand":1,"description":"microRNA 1197 [Source:HGNC Symbol;Acc:HGNC:35376]"}, {"versioned_ensembl_gene_id":"ENSG00000207762.1","gene_symbol":"MIR329-2","gene_name":"microRNA 329-2 [Source:HGNC Symbol;Acc:HGNC:32051]","synonyms":"MIRN329-2,hsa-mir-329-2","biotype":"miRNA","ncbi_id":"574409","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101027100,"end":101027183,"strand":1,"description":"microRNA 329-2 [Source:HGNC Symbol;Acc:HGNC:32051]"}, {"versioned_ensembl_gene_id":"ENSG00000277001.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":91314716,"end":91314997,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202560.4","gene_symbol":"MIR539","gene_name":"microRNA 539 [Source:HGNC Symbol;Acc:HGNC:32529]","synonyms":"MIRN539,hsa-mir-539","biotype":"miRNA","ncbi_id":"664612","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101047321,"end":101047398,"strand":1,"description":"microRNA 539 [Source:HGNC Symbol;Acc:HGNC:32529]"}, {"versioned_ensembl_gene_id":"ENSG00000266517.1","gene_symbol":"MIR4715","gene_name":"microRNA 4715 [Source:HGNC Symbol;Acc:HGNC:41666]","synonyms":"hsa-mir-4715","biotype":"miRNA","ncbi_id":"100616474","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25848747,"end":25848825,"strand":-1,"description":"microRNA 4715 [Source:HGNC Symbol;Acc:HGNC:41666]"}, {"versioned_ensembl_gene_id":"ENSG00000274466.1","gene_symbol":"MIR1273H","gene_name":"microRNA 1273h [Source:HGNC Symbol;Acc:HGNC:49973]","synonyms":"hsa-mir-1273h","biotype":"miRNA","ncbi_id":"102466247","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24203116,"end":24203231,"strand":1,"description":"microRNA 1273h [Source:HGNC Symbol;Acc:HGNC:49973]"}, {"versioned_ensembl_gene_id":"ENSG00000222705.1","gene_symbol":"RN7SKP39","gene_name":"RNA, 7SK small nuclear pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:45763]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480845","summary":null,"start":28442575,"end":28442896,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 39 [Source:HGNC Symbol;Acc:HGNC:45763]"}, {"versioned_ensembl_gene_id":"ENSG00000207166.1","gene_symbol":"SNORA68","gene_name":"small nucleolar RNA, H/ACA box 68 [Source:HGNC Symbol;Acc:HGNC:10225]","synonyms":"RNU68,U68,SNORA68A","biotype":"snoRNA","ncbi_id":"26780","summary":null,"start":17862588,"end":17862720,"strand":1,"description":"small nucleolar RNA, H/ACA box 68 [Source:HGNC Symbol;Acc:HGNC:10225]"}, {"versioned_ensembl_gene_id":"ENSG00000201318.1","gene_symbol":"SNORD114-30","gene_name":"small nucleolar RNA, C/D box 114-30 [Source:HGNC Symbol;Acc:HGNC:33018]","synonyms":"14q(II-30)","biotype":"snoRNA","ncbi_id":"767611","summary":null,"start":100991919,"end":100991990,"strand":1,"description":"small nucleolar RNA, C/D box 114-30 [Source:HGNC Symbol;Acc:HGNC:33018]"}, {"versioned_ensembl_gene_id":"ENSG00000284129.1","gene_symbol":"MIR6789","gene_name":"microRNA 6789 [Source:HGNC Symbol;Acc:HGNC:50094]","synonyms":"hsa-mir-6789","biotype":"miRNA","ncbi_id":"102466736","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2235829,"end":2235926,"strand":-1,"description":"microRNA 6789 [Source:HGNC Symbol;Acc:HGNC:50094]"}, {"versioned_ensembl_gene_id":"ENSG00000207501.1","gene_symbol":"RNVU1-14","gene_name":"RNA, variant U1 small nuclear 14 [Source:HGNC Symbol;Acc:HGNC:48319]","synonyms":"vU1.14,RNU1-37","biotype":"snRNA","ncbi_id":"101954266","summary":null,"start":145281116,"end":145281279,"strand":1,"description":"RNA, variant U1 small nuclear 14 [Source:HGNC Symbol;Acc:HGNC:48319]"}, {"versioned_ensembl_gene_id":"ENSG00000252025.1","gene_symbol":"RNU6-982P","gene_name":"RNA, U6 small nuclear 982, pseudogene [Source:HGNC Symbol;Acc:HGNC:47945]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481979","summary":null,"start":53745004,"end":53745105,"strand":-1,"description":"RNA, U6 small nuclear 982, pseudogene [Source:HGNC Symbol;Acc:HGNC:47945]"}, {"versioned_ensembl_gene_id":"ENSG00000200406.1","gene_symbol":"SNORD114-23","gene_name":"small nucleolar RNA, C/D box 114-23 [Source:HGNC Symbol;Acc:HGNC:33011]","synonyms":"14q(II-23)","biotype":"snoRNA","ncbi_id":"767603","summary":null,"start":100983876,"end":100983947,"strand":1,"description":"small nucleolar RNA, C/D box 114-23 [Source:HGNC Symbol;Acc:HGNC:33011]"}, {"versioned_ensembl_gene_id":"ENSG00000252106.2","gene_symbol":"RNY3P15","gene_name":"RNA, Ro-associated Y3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:50890]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107178919","summary":null,"start":34873831,"end":34873927,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 15 [Source:HGNC Symbol;Acc:HGNC:50890]"}, {"versioned_ensembl_gene_id":"ENSG00000201830.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97915690,"end":97915796,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265510.1","gene_symbol":"MIR4436A","gene_name":"microRNA 4436a [Source:HGNC Symbol;Acc:HGNC:41762]","synonyms":"hsa-mir-4436a","biotype":"miRNA","ncbi_id":"100616399","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":88812370,"end":88812454,"strand":1,"description":"microRNA 4436a [Source:HGNC Symbol;Acc:HGNC:41762]"}, {"versioned_ensembl_gene_id":"ENSG00000222352.1","gene_symbol":"RN7SKP221","gene_name":"RNA, 7SK small nuclear pseudogene 221 [Source:HGNC Symbol;Acc:HGNC:45945]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480474","summary":null,"start":21545344,"end":21545644,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 221 [Source:HGNC Symbol;Acc:HGNC:45945]"}, {"versioned_ensembl_gene_id":"ENSG00000207951.1","gene_symbol":"MIR561","gene_name":"microRNA 561 [Source:HGNC Symbol;Acc:HGNC:32817]","synonyms":"MIRN561,hsa-mir-561","biotype":"miRNA","ncbi_id":"693146","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":188297492,"end":188297588,"strand":1,"description":"microRNA 561 [Source:HGNC Symbol;Acc:HGNC:32817]"}, {"versioned_ensembl_gene_id":"ENSG00000201317.1","gene_symbol":"RNU4-59P","gene_name":"RNA, U4 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:46995]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481764","summary":null,"start":92700819,"end":92700934,"strand":-1,"description":"RNA, U4 small nuclear 59, pseudogene [Source:HGNC Symbol;Acc:HGNC:46995]"}, {"versioned_ensembl_gene_id":"ENSG00000263616.2","gene_symbol":"RN7SL178P","gene_name":"RNA, 7SL, cytoplasmic 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:46194]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479286","summary":null,"start":8582352,"end":8582655,"strand":-1,"description":"RNA, 7SL, cytoplasmic 178, pseudogene [Source:HGNC Symbol;Acc:HGNC:46194]"}, {"versioned_ensembl_gene_id":"ENSG00000263905.2","gene_symbol":"RN7SL555P","gene_name":"RNA, 7SL, cytoplasmic 555, pseudogene [Source:HGNC Symbol;Acc:HGNC:46571]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479424","summary":null,"start":3094171,"end":3094509,"strand":1,"description":"RNA, 7SL, cytoplasmic 555, pseudogene [Source:HGNC Symbol;Acc:HGNC:46571]"}, {"versioned_ensembl_gene_id":"ENSG00000252287.1","gene_symbol":"RNA5SP24","gene_name":"RNA, 5S ribosomal pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42600]","synonyms":"RN5S24","biotype":"rRNA","ncbi_id":"100873356","summary":null,"start":19088487,"end":19088581,"strand":1,"description":"RNA, 5S ribosomal pseudogene 24 [Source:HGNC Symbol;Acc:HGNC:42600]"}, {"versioned_ensembl_gene_id":"ENSG00000206889.1","gene_symbol":"RNU6-1200P","gene_name":"RNA, U6 small nuclear 1200, pseudogene [Source:HGNC Symbol;Acc:HGNC:48163]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481559","summary":null,"start":117544205,"end":117544311,"strand":1,"description":"RNA, U6 small nuclear 1200, pseudogene [Source:HGNC Symbol;Acc:HGNC:48163]"}, {"versioned_ensembl_gene_id":"ENSG00000265470.1","gene_symbol":"MIR548AQ","gene_name":"microRNA 548aq [Source:HGNC Symbol;Acc:HGNC:43488]","synonyms":"hsa-mir-548aq","biotype":"miRNA","ncbi_id":"100847078","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":185767847,"end":185767904,"strand":-1,"description":"microRNA 548aq [Source:HGNC Symbol;Acc:HGNC:43488]"}, {"versioned_ensembl_gene_id":"ENSG00000200713.1","gene_symbol":"RNU6-682P","gene_name":"RNA, U6 small nuclear 682, pseudogene [Source:HGNC Symbol;Acc:HGNC:47645]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479867","summary":null,"start":8895813,"end":8895918,"strand":1,"description":"RNA, U6 small nuclear 682, pseudogene [Source:HGNC Symbol;Acc:HGNC:47645]"}, {"versioned_ensembl_gene_id":"ENSG00000253077.1","gene_symbol":"RNA5SP169","gene_name":"RNA, 5S ribosomal pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:43069]","synonyms":"RN5S169","biotype":"rRNA","ncbi_id":"100873434","summary":null,"start":151971497,"end":151971613,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 169 [Source:HGNC Symbol;Acc:HGNC:43069]"}, {"versioned_ensembl_gene_id":"ENSG00000278316.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":54942120,"end":54966679,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000266509.1","gene_symbol":"MIR3934","gene_name":"microRNA 3934 [Source:HGNC Symbol;Acc:HGNC:38965]","synonyms":"hsa-mir-3934","biotype":"miRNA","ncbi_id":"100500873","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33698128,"end":33698234,"strand":1,"description":"microRNA 3934 [Source:HGNC Symbol;Acc:HGNC:38965]"}, {"versioned_ensembl_gene_id":"ENSG00000200685.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":13686550,"end":13686658,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000239745.3","gene_symbol":"RN7SL790P","gene_name":"RNA, 7SL, cytoplasmic 790, pseudogene [Source:HGNC Symbol;Acc:HGNC:46806]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481136","summary":null,"start":74390692,"end":74390989,"strand":1,"description":"RNA, 7SL, cytoplasmic 790, pseudogene [Source:HGNC Symbol;Acc:HGNC:46806]"}, {"versioned_ensembl_gene_id":"ENSG00000200742.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55651534,"end":55651634,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266502.1","gene_symbol":"MIR5681A","gene_name":"microRNA 5681a [Source:HGNC Symbol;Acc:HGNC:43518]","synonyms":"hsa-mir-5681a","biotype":"miRNA","ncbi_id":"100847058","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74548543,"end":74548617,"strand":1,"description":"microRNA 5681a [Source:HGNC Symbol;Acc:HGNC:43518]"}, {"versioned_ensembl_gene_id":"ENSG00000253096.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":103725728,"end":103725825,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200488.1","gene_symbol":"RN7SKP203","gene_name":"RNA, 7SK small nuclear pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:45927]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479185","summary":null,"start":76445079,"end":76445410,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 203 [Source:HGNC Symbol;Acc:HGNC:45927]"}, {"versioned_ensembl_gene_id":"ENSG00000200448.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":42762860,"end":42762959,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283200.1","gene_symbol":"MIR1206","gene_name":"microRNA 1206 [Source:HGNC Symbol;Acc:HGNC:35272]","synonyms":"MIRN1206,hsa-mir-1206","biotype":"miRNA","ncbi_id":"100302170","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128008898,"end":128008956,"strand":1,"description":"microRNA 1206 [Source:HGNC Symbol;Acc:HGNC:35272]"}, {"versioned_ensembl_gene_id":"ENSG00000278590.1","gene_symbol":"RN7SL113P","gene_name":"RNA, 7SL, cytoplasmic 113, pseudogene [Source:HGNC Symbol;Acc:HGNC:46129]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480951","summary":null,"start":85368282,"end":85368580,"strand":1,"description":"RNA, 7SL, cytoplasmic 113, pseudogene [Source:HGNC Symbol;Acc:HGNC:46129]"}, {"versioned_ensembl_gene_id":"ENSG00000201097.1","gene_symbol":"RNU6-366P","gene_name":"RNA, U6 small nuclear 366, pseudogene [Source:HGNC Symbol;Acc:HGNC:47329]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481294","summary":null,"start":92265702,"end":92265807,"strand":1,"description":"RNA, U6 small nuclear 366, pseudogene [Source:HGNC Symbol;Acc:HGNC:47329]"}, {"versioned_ensembl_gene_id":"ENSG00000266315.1","gene_symbol":"MIR4668","gene_name":"microRNA 4668 [Source:HGNC Symbol;Acc:HGNC:41545]","synonyms":"hsa-mir-4668","biotype":"miRNA","ncbi_id":"100616114","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111932100,"end":111932169,"strand":1,"description":"microRNA 4668 [Source:HGNC Symbol;Acc:HGNC:41545]"}, {"versioned_ensembl_gene_id":"ENSG00000199363.1","gene_symbol":"SNORA63","gene_name":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]","synonyms":"RNE3,E3,RNU107,E3-2,SNORA63A","biotype":"snoRNA","ncbi_id":"6043","summary":null,"start":183453814,"end":183453944,"strand":1,"description":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]"}, {"versioned_ensembl_gene_id":"ENSG00000252302.1","gene_symbol":"RNA5SP147","gene_name":"RNA, 5S ribosomal pseudogene 147 [Source:HGNC Symbol;Acc:HGNC:43047]","synonyms":"RN5S147","biotype":"rRNA","ncbi_id":"100873414","summary":null,"start":176763233,"end":176763341,"strand":1,"description":"RNA, 5S ribosomal pseudogene 147 [Source:HGNC Symbol;Acc:HGNC:43047]"}, {"versioned_ensembl_gene_id":"ENSG00000206802.1","gene_symbol":"RNU6-926P","gene_name":"RNA, U6 small nuclear 926, pseudogene [Source:HGNC Symbol;Acc:HGNC:47889]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481472","summary":null,"start":26190707,"end":26190813,"strand":1,"description":"RNA, U6 small nuclear 926, pseudogene [Source:HGNC Symbol;Acc:HGNC:47889]"}, {"versioned_ensembl_gene_id":"ENSG00000200673.1","gene_symbol":"RN7SKP174","gene_name":"RNA, 7SK small nuclear pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:45898]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479172","summary":null,"start":144849755,"end":144850084,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:45898]"}, {"versioned_ensembl_gene_id":"ENSG00000212027.3","gene_symbol":"MIR374B","gene_name":"microRNA 374b [Source:HGNC Symbol;Acc:HGNC:33665]","synonyms":"MIRN374B,hsa-mir-374b","biotype":"miRNA","ncbi_id":"100126317","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74218547,"end":74218618,"strand":-1,"description":"microRNA 374b [Source:HGNC Symbol;Acc:HGNC:33665]"}, {"versioned_ensembl_gene_id":"ENSG00000201242.1","gene_symbol":"RNY1P1","gene_name":"RNA, Ro-associated Y1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42478]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873802","summary":null,"start":27402476,"end":27402587,"strand":-1,"description":"RNA, Ro-associated Y1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:42478]"}, {"versioned_ensembl_gene_id":"ENSG00000202380.1","gene_symbol":"RNU1-55P","gene_name":"RNA, U1 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48397]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481954","summary":null,"start":5890055,"end":5890212,"strand":1,"description":"RNA, U1 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:48397]"}, {"versioned_ensembl_gene_id":"ENSG00000252532.1","gene_symbol":"RNU7-193P","gene_name":"RNA, U7 small nuclear 193 pseudogene [Source:HGNC Symbol;Acc:HGNC:45727]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481804","summary":null,"start":43458065,"end":43458129,"strand":1,"description":"RNA, U7 small nuclear 193 pseudogene [Source:HGNC Symbol;Acc:HGNC:45727]"}, {"versioned_ensembl_gene_id":"ENSG00000252835.1","gene_symbol":"SCARNA21","gene_name":"small Cajal body-specific RNA 21 [Source:HGNC Symbol;Acc:HGNC:32579]","synonyms":"SCARNA21A,ACA68","biotype":"scaRNA","ncbi_id":"677763","summary":null,"start":7906122,"end":7906260,"strand":1,"description":"small Cajal body-specific RNA 21 [Source:HGNC Symbol;Acc:HGNC:32579]"}, {"versioned_ensembl_gene_id":"ENSG00000251712.3","gene_symbol":"RNU7-20P","gene_name":"RNA, U7 small nuclear 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:34116]","synonyms":"U7.20","biotype":"snRNA","ncbi_id":"100147768","summary":null,"start":148821012,"end":148821073,"strand":1,"description":"RNA, U7 small nuclear 20 pseudogene [Source:HGNC Symbol;Acc:HGNC:34116]"}, {"versioned_ensembl_gene_id":"ENSG00000207225.1","gene_symbol":"RNU6-692P","gene_name":"RNA, U6 small nuclear 692, pseudogene [Source:HGNC Symbol;Acc:HGNC:47655]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479871","summary":null,"start":147408342,"end":147408448,"strand":1,"description":"RNA, U6 small nuclear 692, pseudogene [Source:HGNC Symbol;Acc:HGNC:47655]"}, {"versioned_ensembl_gene_id":"ENSG00000276200.1","gene_symbol":"RN7SL820P","gene_name":"RNA, 7SL, cytoplasmic 820, pseudogene [Source:HGNC Symbol;Acc:HGNC:46836]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480535","summary":null,"start":196289409,"end":196289707,"strand":1,"description":"RNA, 7SL, cytoplasmic 820, pseudogene [Source:HGNC Symbol;Acc:HGNC:46836]"}, {"versioned_ensembl_gene_id":"ENSG00000274079.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA 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{"versioned_ensembl_gene_id":"ENSG00000252624.1","gene_symbol":"RNA5SP409","gene_name":"RNA, 5S ribosomal pseudogene 409 [Source:HGNC Symbol;Acc:HGNC:43309]","synonyms":"RN5S409","biotype":"rRNA","ncbi_id":"100873661","summary":null,"start":35735625,"end":35735733,"strand":1,"description":"RNA, 5S ribosomal pseudogene 409 [Source:HGNC Symbol;Acc:HGNC:43309]"}, {"versioned_ensembl_gene_id":"ENSG00000238941.1","gene_symbol":"RNU6-953P","gene_name":"RNA, U6 small nuclear 953, pseudogene [Source:HGNC Symbol;Acc:HGNC:47916]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479988","summary":null,"start":45354779,"end":45354885,"strand":-1,"description":"RNA, U6 small nuclear 953, pseudogene [Source:HGNC Symbol;Acc:HGNC:47916]"}, {"versioned_ensembl_gene_id":"ENSG00000212345.1","gene_symbol":"RNU6-700P","gene_name":"RNA, U6 small nuclear 700, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252962.1","gene_symbol":"RNU6-993P","gene_name":"RNA, U6 small nuclear 993, pseudogene [Source:HGNC Symbol;Acc:HGNC:47956]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480005","summary":null,"start":2503047,"end":2503141,"strand":-1,"description":"RNA, U6 small nuclear 993, pseudogene [Source:HGNC Symbol;Acc:HGNC:47956]"}, {"versioned_ensembl_gene_id":"ENSG00000201296.1","gene_symbol":"RNU4-41P","gene_name":"RNA, U4 small nuclear 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:46977]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481184","summary":null,"start":98417896,"end":98418038,"strand":-1,"description":"RNA, U4 small nuclear 41, pseudogene [Source:HGNC Symbol;Acc:HGNC:46977]"}, {"versioned_ensembl_gene_id":"ENSG00000207303.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":216351403,"end":216351504,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000274005.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000201469.1","gene_symbol":"RNA5SP379","gene_name":"RNA, 5S ribosomal pseudogene 379 [Source:HGNC Symbol;Acc:HGNC:43279]","synonyms":"RN5S379","biotype":"rRNA","ncbi_id":"100873635","summary":null,"start":132723945,"end":132724057,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 379 [Source:HGNC Symbol;Acc:HGNC:43279]"}, {"versioned_ensembl_gene_id":"ENSG00000207011.1","gene_symbol":"RNY4P13","gene_name":"RNA, Ro-associated Y4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:34063]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100379296","summary":null,"start":30059052,"end":30059147,"strand":-1,"description":"RNA, Ro-associated Y4 pseudogene 13 [Source:HGNC Symbol;Acc:HGNC:34063]"}, {"versioned_ensembl_gene_id":"ENSG00000283249.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA 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[Source:RFAM;Acc:RF02211]"}, {"versioned_ensembl_gene_id":"ENSG00000241487.3","gene_symbol":"RN7SL586P","gene_name":"RNA, 7SL, cytoplasmic 586, pseudogene [Source:HGNC Symbol;Acc:HGNC:46602]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481083","summary":null,"start":73040619,"end":73040914,"strand":-1,"description":"RNA, 7SL, cytoplasmic 586, pseudogene [Source:HGNC Symbol;Acc:HGNC:46602]"}, {"versioned_ensembl_gene_id":"ENSG00000238813.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":166123494,"end":166123597,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252422.1","gene_symbol":"RNA5SP476","gene_name":"RNA, 5S ribosomal pseudogene 476 [Source:HGNC Symbol;Acc:HGNC:43376]","synonyms":"RN5S476","biotype":"rRNA","ncbi_id":"100873718","summary":null,"start":18433842,"end":18433944,"strand":1,"description":"RNA, 5S ribosomal 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{"versioned_ensembl_gene_id":"ENSG00000222488.1","gene_symbol":"RNU6-285P","gene_name":"RNA, U6 small nuclear 285, pseudogene [Source:HGNC Symbol;Acc:HGNC:47248]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479693","summary":null,"start":73018945,"end":73019044,"strand":-1,"description":"RNA, U6 small nuclear 285, pseudogene [Source:HGNC Symbol;Acc:HGNC:47248]"}, {"versioned_ensembl_gene_id":"ENSG00000212541.1","gene_symbol":"RNU6-510P","gene_name":"RNA, U6 small nuclear 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:47473]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481342","summary":null,"start":37991462,"end":37991569,"strand":1,"description":"RNA, U6 small nuclear 510, pseudogene [Source:HGNC Symbol;Acc:HGNC:47473]"}, {"versioned_ensembl_gene_id":"ENSG00000212525.1","gene_symbol":"RNA5SP212","gene_name":"RNA, 5S ribosomal pseudogene 212 [Source:HGNC 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101049550,"end":101049646,"strand":1,"description":"microRNA 655 [Source:HGNC Symbol;Acc:HGNC:32911]"}, {"versioned_ensembl_gene_id":"ENSG00000199865.1","gene_symbol":"RNU6-495P","gene_name":"RNA, U6 small nuclear 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:47458]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481337","summary":null,"start":41377177,"end":41377283,"strand":-1,"description":"RNA, U6 small nuclear 495, pseudogene [Source:HGNC Symbol;Acc:HGNC:47458]"}, {"versioned_ensembl_gene_id":"ENSG00000274755.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":115734392,"end":115734491,"strand":1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000264781.1","gene_symbol":"MIR4537","gene_name":"microRNA 4537 [Source:HGNC Symbol;Acc:HGNC:41682]","synonyms":"hsa-mir-4537","biotype":"miRNA","ncbi_id":"100616422","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105859484,"end":105859553,"strand":-1,"description":"microRNA 4537 [Source:HGNC Symbol;Acc:HGNC:41682]"}, {"versioned_ensembl_gene_id":"ENSG00000242493.3","gene_symbol":"RN7SL37P","gene_name":"RNA, 7SL, cytoplasmic 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46053]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479238","summary":null,"start":37246173,"end":37246479,"strand":-1,"description":"RNA, 7SL, cytoplasmic 37, pseudogene [Source:HGNC Symbol;Acc:HGNC:46053]"}, {"versioned_ensembl_gene_id":"ENSG00000242688.3","gene_symbol":"RN7SL304P","gene_name":"RNA, 7SL, cytoplasmic 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:46320]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479333","summary":null,"start":19970969,"end":19971269,"strand":1,"description":"RNA, 7SL, cytoplasmic 304, pseudogene [Source:HGNC Symbol;Acc:HGNC:46320]"}, {"versioned_ensembl_gene_id":"ENSG00000251831.1","gene_symbol":"RNU6-1114P","gene_name":"RNA, U6 small nuclear 1114, pseudogene [Source:HGNC Symbol;Acc:HGNC:48077]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481531","summary":null,"start":16205014,"end":16205120,"strand":1,"description":"RNA, U6 small nuclear 1114, pseudogene [Source:HGNC Symbol;Acc:HGNC:48077]"}, {"versioned_ensembl_gene_id":"ENSG00000264480.1","gene_symbol":"MIR4714","gene_name":"microRNA 4714 [Source:HGNC Symbol;Acc:HGNC:41763]","synonyms":"hsa-mir-4714","biotype":"miRNA","ncbi_id":"100616432","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98784426,"end":98784502,"strand":1,"description":"microRNA 4714 [Source:HGNC Symbol;Acc:HGNC:41763]"}, {"versioned_ensembl_gene_id":"ENSG00000238606.1","gene_symbol":"RNU7-7P","gene_name":"RNA, U7 small nuclear 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:34103]","synonyms":"U7.7","biotype":"snRNA","ncbi_id":"100147755","summary":null,"start":38608215,"end":38608276,"strand":1,"description":"RNA, U7 small nuclear 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:34103]"}, {"versioned_ensembl_gene_id":"ENSG00000201812.1","gene_symbol":"RNA5SP488","gene_name":"RNA, 5S ribosomal pseudogene 488 [Source:HGNC Symbol;Acc:HGNC:43388]","synonyms":"RN5S488","biotype":"rRNA","ncbi_id":"100873730","summary":null,"start":14070871,"end":14070986,"strand":1,"description":"RNA, 5S ribosomal pseudogene 488 [Source:HGNC Symbol;Acc:HGNC:43388]"}, {"versioned_ensembl_gene_id":"ENSG00000275689.1","gene_symbol":"FAS-AS1","gene_name":"FAS antisense RNA 1 conserved region [Source:RFAM;Acc:RF02116]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100302740","summary":null,"start":21126271,"end":21126396,"strand":-1,"description":"FAS antisense RNA 1 conserved region [Source:RFAM;Acc:RF02116]"}, {"versioned_ensembl_gene_id":"ENSG00000201405.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23370254,"end":23370346,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222598.1","gene_symbol":"RNU2-49P","gene_name":"RNA, U2 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:48542]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480219","summary":null,"start":115774319,"end":115774502,"strand":-1,"description":"RNA, U2 small nuclear 49, pseudogene [Source:HGNC Symbol;Acc:HGNC:48542]"}, {"versioned_ensembl_gene_id":"ENSG00000278739.1","gene_symbol":"MIR6859-4","gene_name":"microRNA 6859-4 [Source:HGNC Symbol;Acc:HGNC:50840]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504738","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17052,"end":17119,"strand":-1,"description":"microRNA 6859-4 [Source:HGNC Symbol;Acc:HGNC:50840]"}, {"versioned_ensembl_gene_id":"ENSG00000200503.1","gene_symbol":"SNORD115-5","gene_name":"small nucleolar RNA, C/D box 115-5 [Source:HGNC Symbol;Acc:HGNC:33024]","synonyms":"HBII-52-5","biotype":"snoRNA","ncbi_id":"100033442","summary":null,"start":25178738,"end":25178819,"strand":1,"description":"small nucleolar RNA, C/D box 115-5 [Source:HGNC Symbol;Acc:HGNC:33024]"}, {"versioned_ensembl_gene_id":"ENSG00000264071.2","gene_symbol":"RN7SL531P","gene_name":"RNA, 7SL, cytoplasmic 531, pseudogene [Source:HGNC Symbol;Acc:HGNC:46547]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479416","summary":null,"start":43492032,"end":43492313,"strand":1,"description":"RNA, 7SL, cytoplasmic 531, pseudogene [Source:HGNC Symbol;Acc:HGNC:46547]"}, {"versioned_ensembl_gene_id":"ENSG00000212383.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":56861375,"end":56861508,"strand":1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000221200.1","gene_symbol":"MIR1253","gene_name":"microRNA 1253 [Source:HGNC Symbol;Acc:HGNC:35318]","synonyms":"MIRN1253,hsa-mir-1253","biotype":"miRNA","ncbi_id":"100302208","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2748078,"end":2748182,"strand":-1,"description":"microRNA 1253 [Source:HGNC Symbol;Acc:HGNC:35318]"}, {"versioned_ensembl_gene_id":"ENSG00000201723.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":78544095,"end":78544188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000273940.1","gene_symbol":"RN7SL722P","gene_name":"RNA, 7SL, cytoplasmic 722, pseudogene [Source:HGNC Symbol;Acc:HGNC:46738]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479486","summary":null,"start":61789143,"end":61789426,"strand":1,"description":"RNA, 7SL, cytoplasmic 722, pseudogene [Source:HGNC Symbol;Acc:HGNC:46738]"}, {"versioned_ensembl_gene_id":"ENSG00000274197.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":130114251,"end":130114335,"strand":-1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000265976.1","gene_symbol":"MIR4725","gene_name":"microRNA 4725 [Source:HGNC Symbol;Acc:HGNC:41608]","synonyms":"hsa-mir-4725","biotype":"miRNA","ncbi_id":"100616449","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31575269,"end":31575358,"strand":1,"description":"microRNA 4725 [Source:HGNC Symbol;Acc:HGNC:41608]"}, {"versioned_ensembl_gene_id":"ENSG00000207360.1","gene_symbol":"RNU6-14P","gene_name":"RNA, U6 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:34258]","synonyms":"RNU6-14","biotype":"snRNA","ncbi_id":"100873746","summary":null,"start":15776181,"end":15776286,"strand":-1,"description":"RNA, U6 small nuclear 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:34258]"}, {"versioned_ensembl_gene_id":"ENSG00000222543.1","gene_symbol":"RN7SKP220","gene_name":"RNA, 7SK small nuclear pseudogene 220 [Source:HGNC Symbol;Acc:HGNC:45944]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480901","summary":null,"start":25393557,"end":25393844,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 220 [Source:HGNC Symbol;Acc:HGNC:45944]"}, {"versioned_ensembl_gene_id":"ENSG00000277055.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46165745,"end":46166022,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265116.1","gene_symbol":"SNORD117","gene_name":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]","synonyms":"U83,U83","biotype":"snoRNA","ncbi_id":"692233","summary":null,"start":31575852,"end":31575927,"strand":-1,"description":"small nucleolar RNA, C/D box 117 [Source:HGNC Symbol;Acc:HGNC:32742]"}, {"versioned_ensembl_gene_id":"ENSG00000283615.1","gene_symbol":"MIR924","gene_name":"microRNA 924 [Source:HGNC Symbol;Acc:HGNC:33674]","synonyms":"MIRN924,hsa-mir-924","biotype":"miRNA","ncbi_id":"100126323","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39622123,"end":39622175,"strand":-1,"description":"microRNA 924 [Source:HGNC Symbol;Acc:HGNC:33674]"}, {"versioned_ensembl_gene_id":"ENSG00000252552.1","gene_symbol":"RNU6-307P","gene_name":"RNA, U6 small nuclear 307, pseudogene [Source:HGNC Symbol;Acc:HGNC:47270]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481276","summary":null,"start":174996524,"end":174996629,"strand":1,"description":"RNA, U6 small nuclear 307, pseudogene [Source:HGNC Symbol;Acc:HGNC:47270]"}, {"versioned_ensembl_gene_id":"ENSG00000238482.1","gene_symbol":"RNU6-1208P","gene_name":"RNA, U6 small nuclear 1208, pseudogene [Source:HGNC Symbol;Acc:HGNC:48171]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480094","summary":null,"start":24777873,"end":24777979,"strand":-1,"description":"RNA, U6 small nuclear 1208, pseudogene [Source:HGNC Symbol;Acc:HGNC:48171]"}, {"versioned_ensembl_gene_id":"ENSG00000264684.1","gene_symbol":"hsa-mir-4773-1","gene_name":"hsa-mir-4773-1 [Source:miRBase;Acc:MI0017415]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":151368334,"end":151368411,"strand":1,"description":"hsa-mir-4773-1 [Source:miRBase;Acc:MI0017415]"}, {"versioned_ensembl_gene_id":"ENSG00000212448.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":95617689,"end":95617786,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283527.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":35769785,"end":35769867,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000266133.1","gene_symbol":"MIR4759","gene_name":"microRNA 4759 [Source:HGNC Symbol;Acc:HGNC:41575]","synonyms":"hsa-mir-4759","biotype":"miRNA","ncbi_id":"100616243","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26953961,"end":26954043,"strand":1,"description":"microRNA 4759 [Source:HGNC Symbol;Acc:HGNC:41575]"}, {"versioned_ensembl_gene_id":"ENSG00000251816.1","gene_symbol":"RNA5SP157","gene_name":"RNA, 5S ribosomal pseudogene 157 [Source:HGNC Symbol;Acc:HGNC:43057]","synonyms":"RN5S157","biotype":"rRNA","ncbi_id":"100873423","summary":null,"start":19181814,"end":19181856,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 157 [Source:HGNC Symbol;Acc:HGNC:43057]"}, {"versioned_ensembl_gene_id":"ENSG00000252040.1","gene_symbol":"snoU109","gene_name":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":68630223,"end":68630354,"strand":-1,"description":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]"}, {"versioned_ensembl_gene_id":"ENSG00000199473.1","gene_symbol":"SNORA63","gene_name":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]","synonyms":"E3,RNU107,E3-2,SNORA63A,RNE3","biotype":"snoRNA","ncbi_id":"6043","summary":null,"start":17373201,"end":17373326,"strand":-1,"description":"Small nucleolar RNA SNORA63 [Source:RFAM;Acc:RF00092]"}, {"versioned_ensembl_gene_id":"ENSG00000276147.1","gene_symbol":"MIR548AY","gene_name":"microRNA 548ay [Source:HGNC Symbol;Acc:HGNC:49943]","synonyms":"hsa-mir-548ay","biotype":"miRNA","ncbi_id":"102465247","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32506283,"end":32506389,"strand":-1,"description":"microRNA 548ay [Source:HGNC Symbol;Acc:HGNC:49943]"}, {"versioned_ensembl_gene_id":"ENSG00000275293.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":21555138,"end":21555457,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199245.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88430442,"end":88430550,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252233.1","gene_symbol":"RN7SKP253","gene_name":"RNA, 7SK small nuclear pseudogene 253 [Source:HGNC Symbol;Acc:HGNC:45977]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479208","summary":null,"start":139794125,"end":139794433,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 253 [Source:HGNC Symbol;Acc:HGNC:45977]"}, {"versioned_ensembl_gene_id":"ENSG00000263705.1","gene_symbol":"MIR5689","gene_name":"microRNA 5689 [Source:HGNC Symbol;Acc:HGNC:43479]","synonyms":"hsa-mir-5689","biotype":"miRNA","ncbi_id":"100846998","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10439717,"end":10439794,"strand":1,"description":"microRNA 5689 [Source:HGNC Symbol;Acc:HGNC:43479]"}, {"versioned_ensembl_gene_id":"ENSG00000201920.1","gene_symbol":"RNA5SP442","gene_name":"RNA, 5S ribosomal pseudogene 442 [Source:HGNC Symbol;Acc:HGNC:43342]","synonyms":"RN5S442","biotype":"rRNA","ncbi_id":"106480768","summary":null,"start":41718154,"end":41718260,"strand":1,"description":"RNA, 5S ribosomal pseudogene 442 [Source:HGNC Symbol;Acc:HGNC:43342]"}, {"versioned_ensembl_gene_id":"ENSG00000276002.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50258443,"end":50258722,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000242079.1","gene_symbol":"RN7SL318P","gene_name":"RNA, 7SL, cytoplasmic 318, pseudogene [Source:HGNC Symbol;Acc:HGNC:46334]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481009","summary":null,"start":5142411,"end":5142707,"strand":-1,"description":"RNA, 7SL, cytoplasmic 318, pseudogene [Source:HGNC Symbol;Acc:HGNC:46334]"}, {"versioned_ensembl_gene_id":"ENSG00000278785.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":84467901,"end":84468147,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000207604.3","gene_symbol":"MIR206","gene_name":"microRNA 206 [Source:HGNC Symbol;Acc:HGNC:31584]","synonyms":"MIRN206,hsa-mir-206","biotype":"miRNA","ncbi_id":"406989","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. Disruption of the encoded miRNA has been implicated in multiple skeletal muscle disorders, including amyotrophic lateral sclerosis (ALS) and Duchenne muscular dystrophy (DMD), as well as in several cancers. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Aug 2017]","start":52144349,"end":52144434,"strand":1,"description":"microRNA 206 [Source:HGNC Symbol;Acc:HGNC:31584]"}, {"versioned_ensembl_gene_id":"ENSG00000207261.1","gene_symbol":"RNU6-738P","gene_name":"RNA, U6 small nuclear 738, pseudogene [Source:HGNC Symbol;Acc:HGNC:47701]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479892","summary":null,"start":27111569,"end":27111674,"strand":1,"description":"RNA, U6 small nuclear 738, pseudogene [Source:HGNC Symbol;Acc:HGNC:47701]"}, {"versioned_ensembl_gene_id":"ENSG00000266004.1","gene_symbol":"SNORA38","gene_name":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]","synonyms":"ACA38,ACA38","biotype":"snoRNA","ncbi_id":"677820","summary":null,"start":31605253,"end":31605384,"strand":1,"description":"small nucleolar RNA, H/ACA box 38 [Source:HGNC Symbol;Acc:HGNC:32631]"}, {"versioned_ensembl_gene_id":"ENSG00000274864.1","gene_symbol":"HOTAIRM1_3","gene_name":"HOX antisense intergenic RNA myeloid 1 conserved region 3 [Source:RFAM;Acc:RF01977]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27099778,"end":27099836,"strand":1,"description":"HOX antisense intergenic RNA myeloid 1 conserved region 3 [Source:RFAM;Acc:RF01977]"}, {"versioned_ensembl_gene_id":"ENSG00000207573.1","gene_symbol":"MIR550A2","gene_name":"microRNA 550a-2 [Source:HGNC Symbol;Acc:HGNC:32805]","synonyms":"MIRN550-2,MIR550-2,hsa-mir-550a-2,hsa-mir-550-2","biotype":"miRNA","ncbi_id":"693134","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32732981,"end":32733077,"strand":1,"description":"microRNA 550a-2 [Source:HGNC Symbol;Acc:HGNC:32805]"}, {"versioned_ensembl_gene_id":"ENSG00000199676.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":35853252,"end":35853364,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222068.1","gene_symbol":"RN7SKP154","gene_name":"RNA, 7SK small nuclear pseudogene 154 [Source:HGNC Symbol;Acc:HGNC:45878]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480881","summary":null,"start":133391109,"end":133391398,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 154 [Source:HGNC Symbol;Acc:HGNC:45878]"}, {"versioned_ensembl_gene_id":"ENSG00000252994.1","gene_symbol":"RNU6-1231P","gene_name":"RNA, U6 small nuclear 1231, pseudogene [Source:HGNC Symbol;Acc:HGNC:48194]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480104","summary":null,"start":102803929,"end":102804031,"strand":1,"description":"RNA, U6 small nuclear 1231, pseudogene [Source:HGNC Symbol;Acc:HGNC:48194]"}, {"versioned_ensembl_gene_id":"ENSG00000284012.1","gene_symbol":"MIR6840","gene_name":"microRNA 6840 [Source:HGNC Symbol;Acc:HGNC:50138]","synonyms":"hsa-mir-6840","biotype":"miRNA","ncbi_id":"102466747","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100356651,"end":100356721,"strand":1,"description":"microRNA 6840 [Source:HGNC Symbol;Acc:HGNC:50138]"}, {"versioned_ensembl_gene_id":"ENSG00000207462.1","gene_symbol":"RNU6-376P","gene_name":"RNA, U6 small nuclear 376, pseudogene [Source:HGNC Symbol;Acc:HGNC:47339]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479732","summary":null,"start":118702342,"end":118702447,"strand":1,"description":"RNA, U6 small nuclear 376, pseudogene [Source:HGNC Symbol;Acc:HGNC:47339]"}, {"versioned_ensembl_gene_id":"ENSG00000212206.1","gene_symbol":"SNORA69","gene_name":"Small nucleolar RNA SNORA69 [Source:RFAM;Acc:RF00265]","synonyms":"U69,RNU69","biotype":"snoRNA","ncbi_id":"26779","summary":"This gene encodes a member of the family of box ACA small nucleolar RNAs, characterized by a consensus ACA motif positioned 3 nucleotides from the 3' end of the RNAs and a double-hairpin structure. The box ACA small nucleolar RNAs may play a role in rRNA maturation. This gene is co-transcribed with the ribosomal protein L39 gene. [provided by RefSeq, Oct 2009]","start":8329583,"end":8329719,"strand":1,"description":"Small nucleolar RNA SNORA69 [Source:RFAM;Acc:RF00265]"}, {"versioned_ensembl_gene_id":"ENSG00000276919.1","gene_symbol":"MEG3_2","gene_name":"Maternally expressed 3 conserved region 2 [Source:RFAM;Acc:RF01872]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":100829350,"end":100829454,"strand":1,"description":"Maternally expressed 3 conserved region 2 [Source:RFAM;Acc:RF01872]"}, {"versioned_ensembl_gene_id":"ENSG00000201746.1","gene_symbol":"RNU6-828P","gene_name":"RNA, U6 small nuclear 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:47791]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479932","summary":null,"start":10163268,"end":10163374,"strand":1,"description":"RNA, U6 small nuclear 828, pseudogene [Source:HGNC Symbol;Acc:HGNC:47791]"}, {"versioned_ensembl_gene_id":"ENSG00000273593.1","gene_symbol":"MIR7160","gene_name":"microRNA 7160 [Source:HGNC Symbol;Acc:HGNC:50028]","synonyms":"hsa-mir-7160","biotype":"miRNA","ncbi_id":"102465695","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2076589,"end":2076640,"strand":1,"description":"microRNA 7160 [Source:HGNC Symbol;Acc:HGNC:50028]"}, {"versioned_ensembl_gene_id":"ENSG00000201867.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34189174,"end":34189275,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251854.1","gene_symbol":"RNU6-507P","gene_name":"RNA, U6 small nuclear 507, pseudogene [Source:HGNC Symbol;Acc:HGNC:47470]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481341","summary":null,"start":149779009,"end":149779108,"strand":-1,"description":"RNA, U6 small nuclear 507, pseudogene [Source:HGNC Symbol;Acc:HGNC:47470]"}, {"versioned_ensembl_gene_id":"ENSG00000264638.1","gene_symbol":"MIR3152","gene_name":"microRNA 3152 [Source:HGNC Symbol;Acc:HGNC:38379]","synonyms":"hsa-mir-3152","biotype":"miRNA","ncbi_id":"100422869","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134850742,"end":134850807,"strand":-1,"description":"microRNA 3689f [Source:HGNC Symbol;Acc:HGNC:41702]"}, {"versioned_ensembl_gene_id":"ENSG00000207480.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88330176,"end":88330278,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222259.1","gene_symbol":"RN7SKP114","gene_name":"RNA, 7SK small nuclear pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:45838]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480868","summary":null,"start":34049966,"end":34050244,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 114 [Source:HGNC Symbol;Acc:HGNC:45838]"}, {"versioned_ensembl_gene_id":"ENSG00000206931.1","gene_symbol":"RNU6-1042P","gene_name":"RNA, U6 small nuclear 1042, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000223263.1","gene_symbol":"RNU6-387P","gene_name":"RNA, U6 small nuclear 387, pseudogene [Source:HGNC Symbol;Acc:HGNC:47350]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481891","summary":null,"start":67417214,"end":67417318,"strand":1,"description":"RNA, U6 small nuclear 387, pseudogene [Source:HGNC Symbol;Acc:HGNC:47350]"}, {"versioned_ensembl_gene_id":"ENSG00000206962.1","gene_symbol":"RNU6-74P","gene_name":"RNA, U6 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:42564]","synonyms":"RNU6-74","biotype":"snRNA","ncbi_id":"106480752","summary":null,"start":41905118,"end":41905224,"strand":1,"description":"RNA, U6 small nuclear 74, pseudogene [Source:HGNC Symbol;Acc:HGNC:42564]"}, {"versioned_ensembl_gene_id":"ENSG00000253098.1","gene_symbol":"RNU7-161P","gene_name":"RNA, U7 small nuclear 161 pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252030.1","gene_symbol":"RNU6-1196P","gene_name":"RNA, U6 small nuclear 1196, pseudogene [Source:HGNC Symbol;Acc:HGNC:48159]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480089","summary":null,"start":153265662,"end":153265755,"strand":-1,"description":"RNA, U6 small nuclear 1196, pseudogene [Source:HGNC Symbol;Acc:HGNC:48159]"}, {"versioned_ensembl_gene_id":"ENSG00000202512.1","gene_symbol":"RN7SKP230","gene_name":"RNA, 7SK small nuclear pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:45954]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479197","summary":null,"start":109699500,"end":109699834,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 230 [Source:HGNC Symbol;Acc:HGNC:45954]"}, {"versioned_ensembl_gene_id":"ENSG00000266634.1","gene_symbol":"MIR3972","gene_name":"microRNA 3972 [Source:HGNC Symbol;Acc:HGNC:41876]","synonyms":"hsa-mir-3972","biotype":"miRNA","ncbi_id":"100616188","summary":"microRNAs (miRNAs) are short (20-24 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17277889,"end":17277975,"strand":1,"description":"microRNA 3972 [Source:HGNC Symbol;Acc:HGNC:41876]"}, {"versioned_ensembl_gene_id":"ENSG00000207444.1","gene_symbol":"SNORD56B","gene_name":"small nucleolar RNA, C/D box 56B [Source:HGNC Symbol;Acc:HGNC:19771]","synonyms":"RNU56B","biotype":"snoRNA","ncbi_id":"319139","summary":null,"start":71398337,"end":71398407,"strand":1,"description":"small nucleolar RNA, C/D box 56B [Source:HGNC Symbol;Acc:HGNC:19771]"}, {"versioned_ensembl_gene_id":"ENSG00000207750.1","gene_symbol":"MIR553","gene_name":"microRNA 553 [Source:HGNC Symbol;Acc:HGNC:32809]","synonyms":"hsa-mir-553,MIRN553","biotype":"miRNA","ncbi_id":"693138","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100281241,"end":100281308,"strand":1,"description":"microRNA 553 [Source:HGNC Symbol;Acc:HGNC:32809]"}, {"versioned_ensembl_gene_id":"ENSG00000252784.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63338263,"end":63338372,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201109.1","gene_symbol":"RNA5SP245","gene_name":"RNA, 5S ribosomal pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:43145]","synonyms":"RN5S245","biotype":"rRNA","ncbi_id":"100873501","summary":null,"start":130027277,"end":130027397,"strand":1,"description":"RNA, 5S ribosomal pseudogene 245 [Source:HGNC Symbol;Acc:HGNC:43145]"}, {"versioned_ensembl_gene_id":"ENSG00000222150.1","gene_symbol":"RNA5SP239","gene_name":"RNA, 5S ribosomal pseudogene 239 [Source:HGNC Symbol;Acc:HGNC:43139]","synonyms":"RN5S239","biotype":"rRNA","ncbi_id":"100873497","summary":null,"start":116944286,"end":116944414,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 239 [Source:HGNC Symbol;Acc:HGNC:43139]"}, {"versioned_ensembl_gene_id":"ENSG00000284485.1","gene_symbol":"MIR205","gene_name":"microRNA 205 [Source:HGNC Symbol;Acc:HGNC:31583]","synonyms":"MIRN205,hsa-mir-205","biotype":"miRNA","ncbi_id":"406988","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":209432133,"end":209432242,"strand":1,"description":"microRNA 205 [Source:HGNC Symbol;Acc:HGNC:31583]"}, {"versioned_ensembl_gene_id":"ENSG00000239580.3","gene_symbol":"RN7SL675P","gene_name":"RNA, 7SL, cytoplasmic 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:46691]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481107","summary":null,"start":69922751,"end":69923047,"strand":-1,"description":"RNA, 7SL, cytoplasmic 675, pseudogene [Source:HGNC Symbol;Acc:HGNC:46691]"}, {"versioned_ensembl_gene_id":"ENSG00000241992.3","gene_symbol":"RN7SL831P","gene_name":"RNA, 7SL, cytoplasmic 831, pseudogene [Source:HGNC Symbol;Acc:HGNC:46847]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481862","summary":null,"start":96583209,"end":96583527,"strand":1,"description":"RNA, 7SL, cytoplasmic 831, pseudogene [Source:HGNC Symbol;Acc:HGNC:46847]"}, {"versioned_ensembl_gene_id":"ENSG00000207789.1","gene_symbol":"MIR26A2","gene_name":"microRNA 26a-2 [Source:HGNC Symbol;Acc:HGNC:31611]","synonyms":"MIRN26A2,hsa-mir-26a-2","biotype":"miRNA","ncbi_id":"407016","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":57824609,"end":57824692,"strand":-1,"description":"microRNA 26a-2 [Source:HGNC Symbol;Acc:HGNC:31611]"}, {"versioned_ensembl_gene_id":"ENSG00000207044.1","gene_symbol":"RNU6-1226P","gene_name":"RNA, U6 small nuclear 1226, pseudogene [Source:HGNC Symbol;Acc:HGNC:48189]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480102","summary":null,"start":112196440,"end":112196546,"strand":-1,"description":"RNA, U6 small nuclear 1226, pseudogene [Source:HGNC Symbol;Acc:HGNC:48189]"}, {"versioned_ensembl_gene_id":"ENSG00000241227.3","gene_symbol":"RN7SL553P","gene_name":"RNA, 7SL, cytoplasmic 553, pseudogene [Source:HGNC Symbol;Acc:HGNC:46569]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480518","summary":null,"start":5252926,"end":5253223,"strand":-1,"description":"RNA, 7SL, cytoplasmic 553, pseudogene [Source:HGNC Symbol;Acc:HGNC:46569]"}, {"versioned_ensembl_gene_id":"ENSG00000265663.1","gene_symbol":"SNORD32B","gene_name":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]","synonyms":"U32B,U32B","biotype":"snoRNA","ncbi_id":"692092","summary":null,"start":29581840,"end":29581923,"strand":1,"description":"small nucleolar RNA, C/D box 32B [Source:HGNC Symbol;Acc:HGNC:32719]"}, {"versioned_ensembl_gene_id":"ENSG00000278770.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":45526466,"end":45526746,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283159.1","gene_symbol":"MIR665","gene_name":"microRNA 665 [Source:HGNC Symbol;Acc:HGNC:33662]","synonyms":"MIRN665,hsa-mir-665","biotype":"miRNA","ncbi_id":"100126315","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100875033,"end":100875104,"strand":1,"description":"microRNA 665 [Source:HGNC Symbol;Acc:HGNC:33662]"}, {"versioned_ensembl_gene_id":"ENSG00000206877.1","gene_symbol":"RNU6-1103P","gene_name":"RNA, U6 small nuclear 1103, pseudogene [Source:HGNC Symbol;Acc:HGNC:48066]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480051","summary":null,"start":24537332,"end":24537438,"strand":1,"description":"RNA, U6 small nuclear 1103, pseudogene [Source:HGNC Symbol;Acc:HGNC:48066]"}, {"versioned_ensembl_gene_id":"ENSG00000206800.1","gene_symbol":"RNY3P7","gene_name":"RNA, Ro-associated Y3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42491]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100862670","summary":null,"start":77623372,"end":77623472,"strand":1,"description":"RNA, Ro-associated Y3 pseudogene 7 [Source:HGNC Symbol;Acc:HGNC:42491]"}, {"versioned_ensembl_gene_id":"ENSG00000252415.1","gene_symbol":"RNU6-1012P","gene_name":"RNA, U6 small nuclear 1012, pseudogene [Source:HGNC Symbol;Acc:HGNC:47975]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481500","summary":null,"start":73679188,"end":73679296,"strand":-1,"description":"RNA, U6 small nuclear 1012, pseudogene [Source:HGNC Symbol;Acc:HGNC:47975]"}, {"versioned_ensembl_gene_id":"ENSG00000199012.2","gene_symbol":"MIR412","gene_name":"microRNA 412 [Source:HGNC Symbol;Acc:HGNC:32064]","synonyms":"MIRN412,hsa-mir-412","biotype":"miRNA","ncbi_id":"574433","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101065447,"end":101065537,"strand":1,"description":"microRNA 412 [Source:HGNC Symbol;Acc:HGNC:32064]"}, {"versioned_ensembl_gene_id":"ENSG00000221023.1","gene_symbol":"RNU6ATAC19P","gene_name":"RNA, U6atac small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:46918]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481165","summary":null,"start":181738606,"end":181738715,"strand":1,"description":"RNA, U6atac small nuclear 19, pseudogene [Source:HGNC Symbol;Acc:HGNC:46918]"}, {"versioned_ensembl_gene_id":"ENSG00000274777.1","gene_symbol":"AC004792.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56848068,"end":56848204,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000253025.1","gene_symbol":"RNU2-12P","gene_name":"RNA, U2 small nuclear 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48505]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480202","summary":null,"start":176243862,"end":176244029,"strand":-1,"description":"RNA, U2 small nuclear 12, pseudogene [Source:HGNC Symbol;Acc:HGNC:48505]"}, {"versioned_ensembl_gene_id":"ENSG00000263413.2","gene_symbol":"MIR4538","gene_name":"microRNA 4538 [Source:HGNC Symbol;Acc:HGNC:41664]","synonyms":"hsa-mir-4538","biotype":"miRNA","ncbi_id":"100616276","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":105858165,"end":105858242,"strand":-1,"description":"microRNA 4538 [Source:HGNC Symbol;Acc:HGNC:41664]"}, {"versioned_ensembl_gene_id":"ENSG00000222589.1","gene_symbol":"RN7SKP159","gene_name":"RNA, 7SK small nuclear pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:45883]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480468","summary":null,"start":5910945,"end":5911236,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 159 [Source:HGNC Symbol;Acc:HGNC:45883]"}, {"versioned_ensembl_gene_id":"ENSG00000266039.1","gene_symbol":"MIR4509-2","gene_name":"microRNA 4509-2 [Source:HGNC Symbol;Acc:HGNC:41537]","synonyms":"hsa-mir-4509-2","biotype":"miRNA","ncbi_id":"100616228","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28426491,"end":28426584,"strand":1,"description":"microRNA 4509-2 [Source:HGNC Symbol;Acc:HGNC:41537]"}, {"versioned_ensembl_gene_id":"ENSG00000202023.1","gene_symbol":"SNORD81","gene_name":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]","synonyms":null,"biotype":"snoRNA","ncbi_id":"26769","summary":null,"start":137287687,"end":137287762,"strand":1,"description":"Small nucleolar RNA SNORD81 [Source:RFAM;Acc:RF00136]"}, {"versioned_ensembl_gene_id":"ENSG00000207123.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62122320,"end":62122421,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284059.1","gene_symbol":"MIR5572","gene_name":"microRNA 5572 [Source:HGNC Symbol;Acc:HGNC:43476]","synonyms":"hsa-mir-5572","biotype":"miRNA","ncbi_id":"100847042","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80581103,"end":80581239,"strand":1,"description":"microRNA 5572 [Source:HGNC Symbol;Acc:HGNC:43476]"}, {"versioned_ensembl_gene_id":"ENSG00000242482.3","gene_symbol":"RN7SL392P","gene_name":"RNA, 7SL, cytoplasmic 392, pseudogene [Source:HGNC Symbol;Acc:HGNC:46408]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480506","summary":null,"start":67656831,"end":67657129,"strand":-1,"description":"RNA, 7SL, cytoplasmic 392, pseudogene [Source:HGNC Symbol;Acc:HGNC:46408]"}, {"versioned_ensembl_gene_id":"ENSG00000263672.2","gene_symbol":"RN7SL750P","gene_name":"RNA, 7SL, cytoplasmic 750, pseudogene [Source:HGNC Symbol;Acc:HGNC:46766]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481126","summary":null,"start":100821027,"end":100821264,"strand":-1,"description":"RNA, 7SL, cytoplasmic 750, pseudogene [Source:HGNC Symbol;Acc:HGNC:46766]"}, {"versioned_ensembl_gene_id":"ENSG00000208003.1","gene_symbol":"MIR549A","gene_name":"microRNA 549a [Source:HGNC Symbol;Acc:HGNC:32803]","synonyms":"hsa-mir-549,MIRN549,MIR549","biotype":"miRNA","ncbi_id":"693132","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80841978,"end":80842073,"strand":-1,"description":"microRNA 549a [Source:HGNC Symbol;Acc:HGNC:32803]"}, {"versioned_ensembl_gene_id":"ENSG00000201628.1","gene_symbol":"RNU4-7P","gene_name":"RNA, U4 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:10194]","synonyms":"U4/7,U4,RNU4P1","biotype":"snRNA","ncbi_id":"6069","summary":null,"start":150326623,"end":150326763,"strand":-1,"description":"RNA, U4 small nuclear 7, pseudogene [Source:HGNC Symbol;Acc:HGNC:10194]"}, {"versioned_ensembl_gene_id":"ENSG00000222706.1","gene_symbol":"RN7SKP89","gene_name":"RNA, 7SK small nuclear pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:45813]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479134","summary":null,"start":114253513,"end":114253754,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 89 [Source:HGNC Symbol;Acc:HGNC:45813]"}, {"versioned_ensembl_gene_id":"ENSG00000212187.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":212025561,"end":212025682,"strand":1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000207614.1","gene_symbol":"MIR193A","gene_name":"microRNA 193a [Source:HGNC Symbol;Acc:HGNC:31563]","synonyms":"MIRN193A,MIRN193,hsa-mir-193a,hsa-mir-193","biotype":"miRNA","ncbi_id":"406968","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31559996,"end":31560083,"strand":1,"description":"microRNA 193a [Source:HGNC Symbol;Acc:HGNC:31563]"}, {"versioned_ensembl_gene_id":"ENSG00000200218.1","gene_symbol":"RNU6-697P","gene_name":"RNA, U6 small nuclear 697, pseudogene [Source:HGNC Symbol;Acc:HGNC:47660]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479874","summary":null,"start":68846805,"end":68846911,"strand":1,"description":"RNA, U6 small nuclear 697, pseudogene [Source:HGNC Symbol;Acc:HGNC:47660]"}, {"versioned_ensembl_gene_id":"ENSG00000243254.3","gene_symbol":"RN7SL350P","gene_name":"RNA, 7SL, cytoplasmic 350, pseudogene [Source:HGNC Symbol;Acc:HGNC:46366]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481019","summary":null,"start":99613783,"end":99614081,"strand":-1,"description":"RNA, 7SL, cytoplasmic 350, pseudogene [Source:HGNC Symbol;Acc:HGNC:46366]"}, {"versioned_ensembl_gene_id":"ENSG00000264010.1","gene_symbol":"MIR4429","gene_name":"microRNA 4429 [Source:HGNC Symbol;Acc:HGNC:41579]","synonyms":"hsa-mir-4429","biotype":"miRNA","ncbi_id":"100616469","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11540605,"end":11540677,"strand":-1,"description":"microRNA 4429 [Source:HGNC Symbol;Acc:HGNC:41579]"}, {"versioned_ensembl_gene_id":"ENSG00000212460.1","gene_symbol":"RNU6-460P","gene_name":"RNA, U6 small nuclear 460, pseudogene [Source:HGNC Symbol;Acc:HGNC:47423]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479769","summary":null,"start":138116573,"end":138116680,"strand":1,"description":"RNA, U6 small nuclear 460, pseudogene [Source:HGNC Symbol;Acc:HGNC:47423]"}, {"versioned_ensembl_gene_id":"ENSG00000199894.1","gene_symbol":"snoU2_19","gene_name":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":110433109,"end":110433188,"strand":-1,"description":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]"}, {"versioned_ensembl_gene_id":"ENSG00000265682.1","gene_symbol":"MIR4267","gene_name":"microRNA 4267 [Source:HGNC Symbol;Acc:HGNC:38286]","synonyms":"hsa-mir-4267","biotype":"miRNA","ncbi_id":"100422994","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110069961,"end":110070042,"strand":-1,"description":"microRNA 4267 [Source:HGNC Symbol;Acc:HGNC:38286]"}, {"versioned_ensembl_gene_id":"ENSG00000243957.3","gene_symbol":"RN7SL647P","gene_name":"RNA, 7SL, cytoplasmic 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:46663]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479458","summary":null,"start":78115158,"end":78115457,"strand":1,"description":"RNA, 7SL, cytoplasmic 647, pseudogene [Source:HGNC Symbol;Acc:HGNC:46663]"}, {"versioned_ensembl_gene_id":"ENSG00000278551.1","gene_symbol":"RNU6-368P","gene_name":"RNA, U6 small nuclear 368, pseudogene [Source:HGNC Symbol;Acc:HGNC:47331]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479729","summary":null,"start":67869947,"end":67870053,"strand":1,"description":"RNA, U6 small nuclear 368, pseudogene [Source:HGNC Symbol;Acc:HGNC:47331]"}, {"versioned_ensembl_gene_id":"ENSG00000242668.3","gene_symbol":"RN7SL317P","gene_name":"RNA, 7SL, cytoplasmic 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:46333]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479338","summary":null,"start":53629713,"end":53630041,"strand":1,"description":"RNA, 7SL, cytoplasmic 317, pseudogene [Source:HGNC Symbol;Acc:HGNC:46333]"}, {"versioned_ensembl_gene_id":"ENSG00000252667.1","gene_symbol":"RNA5SP523","gene_name":"RNA, 5S ribosomal pseudogene 523 [Source:HGNC Symbol;Acc:HGNC:43423]","synonyms":"RN5S523","biotype":"rRNA","ncbi_id":"106480772","summary":null,"start":18348035,"end":18348147,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 523 [Source:HGNC Symbol;Acc:HGNC:43423]"}, {"versioned_ensembl_gene_id":"ENSG00000207264.1","gene_symbol":"RNU6-15P","gene_name":"RNA, U6 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:34259]","synonyms":"RNU6-15","biotype":"snRNA","ncbi_id":"100302741","summary":null,"start":21321961,"end":21322067,"strand":1,"description":"RNA, U6 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:34259]"}, {"versioned_ensembl_gene_id":"ENSG00000278524.1","gene_symbol":"MIR6810","gene_name":"microRNA 6810 [Source:HGNC Symbol;Acc:HGNC:49987]","synonyms":"hsa-mir-6810","biotype":"miRNA","ncbi_id":"102466197","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":218341911,"end":218341980,"strand":1,"description":"microRNA 6810 [Source:HGNC Symbol;Acc:HGNC:49987]"}, {"versioned_ensembl_gene_id":"ENSG00000238440.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":64355762,"end":64355865,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000266464.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33369961,"end":33370056,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000216141.3","gene_symbol":"MIR941-2","gene_name":"microRNA 941-2 [Source:HGNC Symbol;Acc:HGNC:33685]","synonyms":"hsa-mir-941-2,MIRN941-2","biotype":"miRNA","ncbi_id":"100126339","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63919505,"end":63919576,"strand":1,"description":"microRNA 941-2 [Source:HGNC Symbol;Acc:HGNC:33685]"}, {"versioned_ensembl_gene_id":"ENSG00000252503.1","gene_symbol":"RNU6-531P","gene_name":"RNA, U6 small nuclear 531, pseudogene [Source:HGNC Symbol;Acc:HGNC:47494]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479802","summary":null,"start":139055475,"end":139055578,"strand":1,"description":"RNA, U6 small nuclear 531, pseudogene [Source:HGNC Symbol;Acc:HGNC:47494]"}, {"versioned_ensembl_gene_id":"ENSG00000201592.1","gene_symbol":"snoU2_19","gene_name":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":20136306,"end":20136385,"strand":-1,"description":"Small nucleolar RNA U2-19 [Source:RFAM;Acc:RF00494]"}, {"versioned_ensembl_gene_id":"ENSG00000216135.3","gene_symbol":"MIR885","gene_name":"microRNA 885 [Source:HGNC Symbol;Acc:HGNC:33659]","synonyms":"MIRN885,hsa-mir-885","biotype":"miRNA","ncbi_id":"100126334","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10394489,"end":10394562,"strand":-1,"description":"microRNA 885 [Source:HGNC Symbol;Acc:HGNC:33659]"}, {"versioned_ensembl_gene_id":"ENSG00000242315.3","gene_symbol":"RN7SL685P","gene_name":"RNA, 7SL, cytoplasmic 685, pseudogene [Source:HGNC Symbol;Acc:HGNC:46701]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479473","summary":null,"start":100957883,"end":100958180,"strand":1,"description":"RNA, 7SL, cytoplasmic 685, pseudogene [Source:HGNC Symbol;Acc:HGNC:46701]"}, {"versioned_ensembl_gene_id":"ENSG00000252641.2","gene_symbol":"RNU6-678P","gene_name":"RNA, U6 small nuclear 678, pseudogene [Source:HGNC Symbol;Acc:HGNC:47641]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479865","summary":null,"start":133664926,"end":133665034,"strand":1,"description":"RNA, U6 small nuclear 678, pseudogene [Source:HGNC Symbol;Acc:HGNC:47641]"}, {"versioned_ensembl_gene_id":"ENSG00000201498.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34384165,"end":34384265,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283745.1","gene_symbol":"MIR196B","gene_name":"microRNA 196b [Source:HGNC Symbol;Acc:HGNC:31790]","synonyms":"MIRN196B,hsa-mir-196b","biotype":"miRNA","ncbi_id":"442920","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27169480,"end":27169563,"strand":-1,"description":"microRNA 196b [Source:HGNC Symbol;Acc:HGNC:31790]"}, {"versioned_ensembl_gene_id":"ENSG00000206957.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44697333,"end":44697430,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272034.1","gene_symbol":"SNORD14A","gene_name":"small nucleolar RNA, C/D box 14A [Source:HGNC Symbol;Acc:HGNC:10113]","synonyms":"U14,RNU14A,RNU14","biotype":"snoRNA","ncbi_id":"26822","summary":null,"start":17074654,"end":17074744,"strand":-1,"description":"small nucleolar RNA, C/D box 14A [Source:HGNC Symbol;Acc:HGNC:10113]"}, {"versioned_ensembl_gene_id":"ENSG00000283956.1","gene_symbol":"MIR3610","gene_name":"microRNA 3610 [Source:HGNC Symbol;Acc:HGNC:38942]","synonyms":"hsa-mir-3610","biotype":"miRNA","ncbi_id":"100500914","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116874728,"end":116874800,"strand":-1,"description":"microRNA 3610 [Source:HGNC Symbol;Acc:HGNC:38942]"}, {"versioned_ensembl_gene_id":"ENSG00000200564.1","gene_symbol":"SNORD115-39","gene_name":"small nucleolar RNA, C/D box 115-39 [Source:HGNC Symbol;Acc:HGNC:33058]","synonyms":"HBII-52-39","biotype":"snoRNA","ncbi_id":"100033813","summary":null,"start":25241746,"end":25241827,"strand":1,"description":"small nucleolar RNA, C/D box 115-39 [Source:HGNC Symbol;Acc:HGNC:33058]"}, {"versioned_ensembl_gene_id":"ENSG00000221768.2","gene_symbol":"MIR1302-7","gene_name":"microRNA 1302-7 [Source:HGNC Symbol;Acc:HGNC:35299]","synonyms":"MIRN1302-7,hsa-mir-1302-7","biotype":"miRNA","ncbi_id":"100302147","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":141786242,"end":141786313,"strand":-1,"description":"microRNA 1302-7 [Source:HGNC Symbol;Acc:HGNC:35299]"}, {"versioned_ensembl_gene_id":"ENSG00000277196.4","gene_symbol":"AC007325.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":138082,"end":161852,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000200594.1","gene_symbol":"RNU6-824P","gene_name":"RNA, U6 small nuclear 824, pseudogene [Source:HGNC Symbol;Acc:HGNC:47787]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480612","summary":null,"start":154825176,"end":154825279,"strand":-1,"description":"RNA, U6 small nuclear 824, pseudogene [Source:HGNC Symbol;Acc:HGNC:47787]"}, {"versioned_ensembl_gene_id":"ENSG00000237611.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7239781,"end":7240018,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199072.3","gene_symbol":"MIRLET7F1","gene_name":"microRNA let-7f-1 [Source:HGNC Symbol;Acc:HGNC:31483]","synonyms":"MIRNLET7F1,hsa-let-7f-1","biotype":"miRNA","ncbi_id":"406888","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94176347,"end":94176433,"strand":1,"description":"microRNA let-7f-1 [Source:HGNC Symbol;Acc:HGNC:31483]"}, {"versioned_ensembl_gene_id":"ENSG00000222118.1","gene_symbol":"RNA5SP487","gene_name":"RNA, 5S ribosomal pseudogene 487 [Source:HGNC Symbol;Acc:HGNC:43387]","synonyms":"RN5S487","biotype":"rRNA","ncbi_id":"100873729","summary":null,"start":56205052,"end":56205173,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 487 [Source:HGNC Symbol;Acc:HGNC:43387]"}, {"versioned_ensembl_gene_id":"ENSG00000252906.1","gene_symbol":"SCARNA3","gene_name":"small Cajal body-specific RNA 3 [Source:HGNC Symbol;Acc:HGNC:32577]","synonyms":"HBI-100","biotype":"scaRNA","ncbi_id":"677679","summary":null,"start":175968398,"end":175968540,"strand":-1,"description":"small Cajal body-specific RNA 3 [Source:HGNC Symbol;Acc:HGNC:32577]"}, {"versioned_ensembl_gene_id":"ENSG00000199051.3","gene_symbol":"MIR361","gene_name":"microRNA 361 [Source:HGNC Symbol;Acc:HGNC:31867]","synonyms":"MIRN361,hsa-mir-361","biotype":"miRNA","ncbi_id":"494323","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85903636,"end":85903707,"strand":-1,"description":"microRNA 361 [Source:HGNC Symbol;Acc:HGNC:31867]"}, {"versioned_ensembl_gene_id":"ENSG00000276757.1","gene_symbol":"RN7SL192P","gene_name":"RNA, 7SL, cytoplasmic 192, pseudogene [Source:HGNC Symbol;Acc:HGNC:46208]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480974","summary":null,"start":11011708,"end":11012006,"strand":1,"description":"RNA, 7SL, cytoplasmic 192, pseudogene [Source:HGNC Symbol;Acc:HGNC:46208]"}, {"versioned_ensembl_gene_id":"ENSG00000201863.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":40082983,"end":40083106,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000216171.1","gene_symbol":"MIR513C","gene_name":"microRNA 513c [Source:HGNC Symbol;Acc:HGNC:33934]","synonyms":"MIRN513C,hsa-mir-513c","biotype":"miRNA","ncbi_id":"100302114","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147189704,"end":147189787,"strand":-1,"description":"microRNA 513c [Source:HGNC Symbol;Acc:HGNC:33934]"}, {"versioned_ensembl_gene_id":"ENSG00000206841.1","gene_symbol":"RNU6-409P","gene_name":"RNA, U6 small nuclear 409, pseudogene [Source:HGNC Symbol;Acc:HGNC:47372]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481307","summary":null,"start":50691260,"end":50691363,"strand":-1,"description":"RNA, U6 small nuclear 409, pseudogene [Source:HGNC Symbol;Acc:HGNC:47372]"}, {"versioned_ensembl_gene_id":"ENSG00000273886.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34910545,"end":34910815,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265918.2","gene_symbol":"RN7SL543P","gene_name":"RNA, 7SL, cytoplasmic 543, pseudogene 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{"versioned_ensembl_gene_id":"ENSG00000252889.1","gene_symbol":"RNU6-1236P","gene_name":"RNA, U6 small nuclear 1236, pseudogene [Source:HGNC Symbol;Acc:HGNC:48199]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481570","summary":null,"start":109225129,"end":109225227,"strand":1,"description":"RNA, U6 small nuclear 1236, pseudogene [Source:HGNC Symbol;Acc:HGNC:48199]"}, {"versioned_ensembl_gene_id":"ENSG00000265078.2","gene_symbol":"RN7SL664P","gene_name":"RNA, 7SL, cytoplasmic 664, pseudogene [Source:HGNC Symbol;Acc:HGNC:46680]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479464","summary":null,"start":48094801,"end":48095105,"strand":-1,"description":"RNA, 7SL, cytoplasmic 664, pseudogene [Source:HGNC Symbol;Acc:HGNC:46680]"}, {"versioned_ensembl_gene_id":"ENSG00000280773.2","gene_symbol":"MIR7641-1","gene_name":"microRNA 7641-1 [Source:HGNC Symbol;Acc:HGNC:49995]","synonyms":"hsa-mir-7641-1","biotype":"miRNA","ncbi_id":"102465752","summary":"This record was withdrawn by miRBase.","start":104252591,"end":104252651,"strand":1,"description":"microRNA 7641-1 [Source:HGNC Symbol;Acc:HGNC:49995]"}, {"versioned_ensembl_gene_id":"ENSG00000275123.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000252713.1","gene_symbol":"RNU6-1198P","gene_name":"RNA, U6 small nuclear 1198, pseudogene [Source:HGNC Symbol;Acc:HGNC:48161]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480090","summary":null,"start":73507208,"end":73507274,"strand":1,"description":"RNA, U6 small nuclear 1198, pseudogene [Source:HGNC Symbol;Acc:HGNC:48161]"}, {"versioned_ensembl_gene_id":"ENSG00000222614.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46736312,"end":46736419,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278596.1","gene_symbol":"MIR6077","gene_name":"microRNA 6077 [Source:HGNC Symbol;Acc:HGNC:50025]","synonyms":"MIR6077-2,MIR6077-1,hsa-mir-6077-2,hsa-mir-6077-1","biotype":"miRNA","ncbi_id":"102466225","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":148388282,"end":148388363,"strand":1,"description":"microRNA 6077 [Source:HGNC Symbol;Acc:HGNC:50025]"}, {"versioned_ensembl_gene_id":"ENSG00000212452.1","gene_symbol":"SNORD69","gene_name":"small nucleolar RNA, C/D box 69 [Source:HGNC Symbol;Acc:HGNC:32730]","synonyms":"HBII-210","biotype":"snoRNA","ncbi_id":"692109","summary":null,"start":52692736,"end":52692812,"strand":1,"description":"small nucleolar RNA, C/D box 69 [Source:HGNC Symbol;Acc:HGNC:32730]"}, {"versioned_ensembl_gene_id":"ENSG00000283799.1","gene_symbol":"MIR1182","gene_name":"microRNA 1182 [Source:HGNC Symbol;Acc:HGNC:35263]","synonyms":"MIRN1182,hsa-mir-1182","biotype":"miRNA","ncbi_id":"100302132","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":231019828,"end":231019924,"strand":-1,"description":"microRNA 1182 [Source:HGNC Symbol;Acc:HGNC:35263]"}, {"versioned_ensembl_gene_id":"ENSG00000276066.4","gene_symbol":"VSTM1","gene_name":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]","synonyms":"UNQ3033","biotype":"protein_coding","ncbi_id":"284415","summary":null,"start":54040833,"end":54063953,"strand":-1,"description":"V-set and transmembrane domain containing 1 [Source:HGNC Symbol;Acc:HGNC:29455]"}, {"versioned_ensembl_gene_id":"ENSG00000265684.2","gene_symbol":"RN7SL378P","gene_name":"RNA, 7SL, cytoplasmic 378, pseudogene [Source:HGNC Symbol;Acc:HGNC:46394]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481026","summary":null,"start":82078427,"end":82078724,"strand":1,"description":"RNA, 7SL, cytoplasmic 378, pseudogene [Source:HGNC Symbol;Acc:HGNC:46394]"}, {"versioned_ensembl_gene_id":"ENSG00000264572.1","gene_symbol":"MIR4296","gene_name":"microRNA 4296 [Source:HGNC Symbol;Acc:HGNC:38178]","synonyms":"hsa-mir-4296","biotype":"miRNA","ncbi_id":"100423041","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":125032783,"end":125032870,"strand":-1,"description":"microRNA 4296 [Source:HGNC Symbol;Acc:HGNC:38178]"}, {"versioned_ensembl_gene_id":"ENSG00000284108.1","gene_symbol":"MIR611","gene_name":"microRNA 611 [Source:HGNC Symbol;Acc:HGNC:32867]","synonyms":"MIRN611,hsa-mir-611","biotype":"miRNA","ncbi_id":"693196","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":61792495,"end":61792561,"strand":-1,"description":"microRNA 611 [Source:HGNC Symbol;Acc:HGNC:32867]"}, {"versioned_ensembl_gene_id":"ENSG00000202377.1","gene_symbol":"SNORA25B","gene_name":"small nucleolar RNA, H/ACA box 25B [Source:HGNC Symbol;Acc:HGNC:52199]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109623459","summary":null,"start":115581315,"end":115581442,"strand":-1,"description":"small nucleolar RNA, H/ACA box 25B [Source:HGNC Symbol;Acc:HGNC:52199]"}, {"versioned_ensembl_gene_id":"ENSG00000265874.1","gene_symbol":"MIR4489","gene_name":"microRNA 4489 [Source:HGNC Symbol;Acc:HGNC:41685]","synonyms":"hsa-mir-4489","biotype":"miRNA","ncbi_id":"100616284","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65649192,"end":65649253,"strand":1,"description":"microRNA 4489 [Source:HGNC Symbol;Acc:HGNC:41685]"}, {"versioned_ensembl_gene_id":"ENSG00000273748.1","gene_symbol":"AL592183.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54224,"end":83311,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000222139.1","gene_symbol":"RNU6-380P","gene_name":"RNA, U6 small nuclear 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:47343]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481298","summary":null,"start":80663772,"end":80663878,"strand":1,"description":"RNA, U6 small nuclear 380, pseudogene [Source:HGNC Symbol;Acc:HGNC:47343]"}, {"versioned_ensembl_gene_id":"ENSG00000275022.1","gene_symbol":"MIR6753","gene_name":"microRNA 6753 [Source:HGNC Symbol;Acc:HGNC:50255]","synonyms":"hsa-mir-6753","biotype":"miRNA","ncbi_id":"102465451","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":68044794,"end":68044957,"strand":1,"description":"microRNA 6753 [Source:HGNC Symbol;Acc:HGNC:50255]"}, {"versioned_ensembl_gene_id":"ENSG00000278189.1","gene_symbol":"RNA5-8SN5","gene_name":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]","synonyms":null,"biotype":"rRNA","ncbi_id":"100008587","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. This gene is a representative copy of the 5.8S ribosomal RNA whose chromosomal location is unknown. [provided by RefSeq, Mar 2017]","start":8439823,"end":8439975,"strand":1,"description":"RNA, 5.8S ribosomal N5 [Source:HGNC Symbol;Acc:HGNC:53533]"}, {"versioned_ensembl_gene_id":"ENSG00000283603.1","gene_symbol":"MIR4302","gene_name":"microRNA 4302 [Source:HGNC Symbol;Acc:HGNC:38185]","synonyms":"hsa-mir-4302","biotype":"miRNA","ncbi_id":"100422897","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25874020,"end":25874079,"strand":-1,"description":"microRNA 4302 [Source:HGNC Symbol;Acc:HGNC:38185]"}, {"versioned_ensembl_gene_id":"ENSG00000281228.1","gene_symbol":"AL132640.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":67616903,"end":67617084,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000264387.1","gene_symbol":"MIR5007","gene_name":"microRNA 5007 [Source:HGNC Symbol;Acc:HGNC:43468]","synonyms":"hsa-mir-5007","biotype":"miRNA","ncbi_id":"100846996","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":55174454,"end":55174548,"strand":1,"description":"microRNA 5007 [Source:HGNC Symbol;Acc:HGNC:43468]"}, {"versioned_ensembl_gene_id":"ENSG00000252704.1","gene_symbol":"RN7SKP277","gene_name":"RNA, 7SK small nuclear pseudogene 277 [Source:HGNC Symbol;Acc:HGNC:46001]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479219","summary":null,"start":121736443,"end":121736725,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 277 [Source:HGNC Symbol;Acc:HGNC:46001]"}, {"versioned_ensembl_gene_id":"ENSG00000283783.1","gene_symbol":"MIR622","gene_name":"microRNA 622 [Source:HGNC Symbol;Acc:HGNC:32878]","synonyms":"MIRN622,hsa-mir-622","biotype":"miRNA","ncbi_id":"693207","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90231182,"end":90231277,"strand":1,"description":"microRNA 622 [Source:HGNC Symbol;Acc:HGNC:32878]"}, {"versioned_ensembl_gene_id":"ENSG00000222613.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":140779039,"end":140779141,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266589.1","gene_symbol":"MIR4512","gene_name":"microRNA 4512 [Source:HGNC Symbol;Acc:HGNC:41701]","synonyms":"hsa-mir-4512","biotype":"miRNA","ncbi_id":"100616149","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66496958,"end":66497034,"strand":-1,"description":"microRNA 4512 [Source:HGNC Symbol;Acc:HGNC:41701]"}, {"versioned_ensembl_gene_id":"ENSG00000265031.1","gene_symbol":"MIR1273E","gene_name":"microRNA 1273e [Source:HGNC Symbol;Acc:HGNC:50833]","synonyms":null,"biotype":"miRNA","ncbi_id":"100526648","summary":"This record was withdrawn by miRBase.","start":64425069,"end":64425170,"strand":-1,"description":"microRNA 1273e [Source:HGNC Symbol;Acc:HGNC:50833]"}, {"versioned_ensembl_gene_id":"ENSG00000200818.1","gene_symbol":"RNU6-1204P","gene_name":"RNA, U6 small nuclear 1204, pseudogene [Source:HGNC Symbol;Acc:HGNC:48167]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481560","summary":null,"start":56824986,"end":56825092,"strand":1,"description":"RNA, U6 small nuclear 1204, pseudogene [Source:HGNC Symbol;Acc:HGNC:48167]"}, {"versioned_ensembl_gene_id":"ENSG00000243671.3","gene_symbol":"RN7SL761P","gene_name":"RNA, 7SL, cytoplasmic 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:46777]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479499","summary":null,"start":68693804,"end":68694081,"strand":-1,"description":"RNA, 7SL, cytoplasmic 761, pseudogene [Source:HGNC Symbol;Acc:HGNC:46777]"}, {"versioned_ensembl_gene_id":"ENSG00000265444.1","gene_symbol":"MIR4733","gene_name":"microRNA 4733 [Source:HGNC Symbol;Acc:HGNC:41638]","synonyms":"hsa-mir-4733","biotype":"miRNA","ncbi_id":"100616266","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31094350,"end":31094425,"strand":-1,"description":"microRNA 4733 [Source:HGNC Symbol;Acc:HGNC:41638]"}, {"versioned_ensembl_gene_id":"ENSG00000271924.1","gene_symbol":"RNA5SP108","gene_name":"RNA, 5S ribosomal pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:42906]","synonyms":"RN5S108","biotype":"rRNA","ncbi_id":"100873378","summary":null,"start":161409554,"end":161409670,"strand":1,"description":"RNA, 5S ribosomal pseudogene 108 [Source:HGNC Symbol;Acc:HGNC:42906]"}, {"versioned_ensembl_gene_id":"ENSG00000274054.1","gene_symbol":"MIR4727","gene_name":"microRNA 4727 [Source:HGNC Symbol;Acc:HGNC:41709]","synonyms":"hsa-mir-4727","biotype":"miRNA","ncbi_id":"100616416","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38825838,"end":38825892,"strand":1,"description":"microRNA 4727 [Source:HGNC Symbol;Acc:HGNC:41709]"}, {"versioned_ensembl_gene_id":"ENSG00000283218.1","gene_symbol":"MIR302F","gene_name":"microRNA 302f [Source:HGNC Symbol;Acc:HGNC:35349]","synonyms":"MIRN302F,hsa-mir-302f","biotype":"miRNA","ncbi_id":"100302131","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30298910,"end":30298960,"strand":1,"description":"microRNA 302f [Source:HGNC Symbol;Acc:HGNC:35349]"}, {"versioned_ensembl_gene_id":"ENSG00000206698.1","gene_symbol":"RNU1-73P","gene_name":"RNA, U1 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:48415]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481616","summary":null,"start":97175950,"end":97176113,"strand":-1,"description":"RNA, U1 small nuclear 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:48415]"}, {"versioned_ensembl_gene_id":"ENSG00000207585.1","gene_symbol":"MIR181D","gene_name":"microRNA 181d [Source:HGNC Symbol;Acc:HGNC:32089]","synonyms":"MIRN181D,hsa-mir-181d","biotype":"miRNA","ncbi_id":"574457","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":13874875,"end":13875011,"strand":1,"description":"microRNA 181d [Source:HGNC Symbol;Acc:HGNC:32089]"}, {"versioned_ensembl_gene_id":"ENSG00000266559.1","gene_symbol":"MIR4530","gene_name":"microRNA 4530 [Source:HGNC Symbol;Acc:HGNC:41764]","synonyms":"hsa-mir-4530","biotype":"miRNA","ncbi_id":"100616163","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39409623,"end":39409678,"strand":-1,"description":"microRNA 4530 [Source:HGNC Symbol;Acc:HGNC:41764]"}, {"versioned_ensembl_gene_id":"ENSG00000222872.1","gene_symbol":"RNU4-78P","gene_name":"RNA, U4 small nuclear 78, pseudogene [Source:HGNC Symbol;Acc:HGNC:47014]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479594","summary":null,"start":42221840,"end":42221965,"strand":1,"description":"RNA, U4 small nuclear 78, pseudogene [Source:HGNC Symbol;Acc:HGNC:47014]"}, {"versioned_ensembl_gene_id":"ENSG00000207598.1","gene_symbol":"MIR124-3","gene_name":"microRNA 124-3 [Source:HGNC Symbol;Acc:HGNC:31504]","synonyms":"MIRN124A3,MIRN124-3,hsa-mir-124a-3,hsa-mir-124-3","biotype":"miRNA","ncbi_id":"406909","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63178500,"end":63178586,"strand":1,"description":"microRNA 124-3 [Source:HGNC Symbol;Acc:HGNC:31504]"}, {"versioned_ensembl_gene_id":"ENSG00000264534.3","gene_symbol":"MIR378B","gene_name":"microRNA 378b [Source:HGNC Symbol;Acc:HGNC:38283]","synonyms":"hsa-mir-378b","biotype":"miRNA","ncbi_id":"100422933","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10330229,"end":10330285,"strand":1,"description":"microRNA 378b [Source:HGNC Symbol;Acc:HGNC:38283]"}, {"versioned_ensembl_gene_id":"ENSG00000200688.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":112069104,"end":112069209,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278103.1","gene_symbol":"MIR8060","gene_name":"microRNA 8060 [Source:HGNC Symbol;Acc:HGNC:50180]","synonyms":"hsa-mir-8060","biotype":"miRNA","ncbi_id":"102465864","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":96359964,"end":96360039,"strand":1,"description":"microRNA 8060 [Source:HGNC Symbol;Acc:HGNC:50180]"}, {"versioned_ensembl_gene_id":"ENSG00000283207.1","gene_symbol":"MIR1255B1","gene_name":"microRNA 1255b-1 [Source:HGNC Symbol;Acc:HGNC:35366]","synonyms":"hsa-mir-1255b-1,MIRN1255B1","biotype":"miRNA","ncbi_id":"100313806","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36426366,"end":36426428,"strand":-1,"description":"microRNA 1255b-1 [Source:HGNC Symbol;Acc:HGNC:35366]"}, {"versioned_ensembl_gene_id":"ENSG00000266270.1","gene_symbol":"MIR5096","gene_name":"microRNA 5096 [Source:HGNC Symbol;Acc:HGNC:41611]","synonyms":"hsa-mir-5096","biotype":"miRNA","ncbi_id":"100616427","summary":"This record was withdrawn by miRBase.","start":78820752,"end":78820821,"strand":1,"description":"microRNA 5096 [Source:HGNC Symbol;Acc:HGNC:41611]"}, {"versioned_ensembl_gene_id":"ENSG00000199036.1","gene_symbol":"MIR219A1","gene_name":"microRNA 219a-1 [Source:HGNC Symbol;Acc:HGNC:31597]","synonyms":"MIRN219-1,MIR219-1,hsa-mir-219-1","biotype":"miRNA","ncbi_id":"407002","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33207835,"end":33207944,"strand":1,"description":"microRNA 219a-1 [Source:HGNC Symbol;Acc:HGNC:31597]"}, {"versioned_ensembl_gene_id":"ENSG00000212512.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":202070841,"end":202070943,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199177.1","gene_symbol":"MIR31","gene_name":"microRNA 31 [Source:HGNC Symbol;Acc:HGNC:31630]","synonyms":"MIRN31,hsa-mir-31","biotype":"miRNA","ncbi_id":"407035","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21512115,"end":21512185,"strand":-1,"description":"microRNA 31 [Source:HGNC Symbol;Acc:HGNC:31630]"}, {"versioned_ensembl_gene_id":"ENSG00000266855.1","gene_symbol":"MIR3910-1","gene_name":"microRNA 3910-1 [Source:HGNC Symbol;Acc:HGNC:38966]","synonyms":"hsa-mir-3910-1","biotype":"miRNA","ncbi_id":"100500821","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":91636251,"end":91636361,"strand":1,"description":"microRNA 3910-1 [Source:HGNC Symbol;Acc:HGNC:38966]"}, {"versioned_ensembl_gene_id":"ENSG00000273710.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28915579,"end":28915864,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000264823.3","gene_symbol":"MIR3154","gene_name":"microRNA 3154 [Source:HGNC Symbol;Acc:HGNC:38176]","synonyms":"hsa-mir-3154","biotype":"miRNA","ncbi_id":"100422893","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":128244947,"end":128245030,"strand":-1,"description":"microRNA 3154 [Source:HGNC Symbol;Acc:HGNC:38176]"}, {"versioned_ensembl_gene_id":"ENSG00000264955.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31766178,"end":31766266,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000221466.2","gene_symbol":"MIR548AJ2","gene_name":"microRNA 548aj-2 [Source:HGNC Symbol;Acc:HGNC:41600]","synonyms":"hsa-mir-548aj-2","biotype":"miRNA","ncbi_id":"100616252","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38023895,"end":38023986,"strand":-1,"description":"microRNA 548aj-2 [Source:HGNC Symbol;Acc:HGNC:41600]"}, {"versioned_ensembl_gene_id":"ENSG00000211583.3","gene_symbol":"MIR767","gene_name":"microRNA 767 [Source:HGNC Symbol;Acc:HGNC:33136]","synonyms":"MIRN767,hsa-mir-767","biotype":"miRNA","ncbi_id":"768215","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":152393421,"end":152393529,"strand":-1,"description":"microRNA 767 [Source:HGNC Symbol;Acc:HGNC:33136]"}, {"versioned_ensembl_gene_id":"ENSG00000252647.1","gene_symbol":"RNA5SP416","gene_name":"RNA, 5S ribosomal pseudogene 416 [Source:HGNC Symbol;Acc:HGNC:43316]","synonyms":"RN5S416","biotype":"rRNA","ncbi_id":"100873667","summary":null,"start":35751574,"end":35751684,"strand":1,"description":"RNA, 5S ribosomal pseudogene 416 [Source:HGNC Symbol;Acc:HGNC:43316]"}, {"versioned_ensembl_gene_id":"ENSG00000199831.1","gene_symbol":"RN7SKP291","gene_name":"RNA, 7SK small nuclear pseudogene 291 [Source:HGNC Symbol;Acc:HGNC:46015]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480922","summary":null,"start":55376526,"end":55376852,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 291 [Source:HGNC Symbol;Acc:HGNC:46015]"}, {"versioned_ensembl_gene_id":"ENSG00000239149.1","gene_symbol":"SNORA59A","gene_name":"small nucleolar RNA, H/ACA box 59A [Source:HGNC Symbol;Acc:HGNC:32653]","synonyms":"ACA59","biotype":"snoRNA","ncbi_id":"677885","summary":null,"start":12507246,"end":12507397,"strand":1,"description":"small nucleolar RNA, H/ACA box 59A [Source:HGNC Symbol;Acc:HGNC:32653]"}, {"versioned_ensembl_gene_id":"ENSG00000242118.3","gene_symbol":"RN7SL201P","gene_name":"RNA, 7SL, cytoplasmic 201, pseudogene [Source:HGNC Symbol;Acc:HGNC:46217]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481830","summary":null,"start":81967079,"end":81967374,"strand":1,"description":"RNA, 7SL, cytoplasmic 201, pseudogene [Source:HGNC Symbol;Acc:HGNC:46217]"}, {"versioned_ensembl_gene_id":"ENSG00000251892.1","gene_symbol":"RNU7-84P","gene_name":"RNA, U7 small nuclear 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:34180]","synonyms":"U7.84","biotype":"snRNA","ncbi_id":"100151681","summary":null,"start":106729795,"end":106729856,"strand":-1,"description":"RNA, U7 small nuclear 84 pseudogene [Source:HGNC Symbol;Acc:HGNC:34180]"}, {"versioned_ensembl_gene_id":"ENSG00000201356.1","gene_symbol":"RNA5SP500","gene_name":"RNA, 5S ribosomal pseudogene 500 [Source:HGNC Symbol;Acc:HGNC:43400]","synonyms":"RN5S500","biotype":"rRNA","ncbi_id":"100873551","summary":null,"start":28982852,"end":28982970,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 500 [Source:HGNC Symbol;Acc:HGNC:43400]"}, {"versioned_ensembl_gene_id":"ENSG00000221303.1","gene_symbol":"SNORA79","gene_name":"small nucleolar RNA, H/ACA box 79 [Source:HGNC Symbol;Acc:HGNC:32665]","synonyms":"SNORA79A,ACA65","biotype":"snoRNA","ncbi_id":"677845","summary":null,"start":81202695,"end":81202834,"strand":-1,"description":"small nucleolar RNA, H/ACA box 79 [Source:HGNC Symbol;Acc:HGNC:32665]"}, {"versioned_ensembl_gene_id":"ENSG00000275644.4","gene_symbol":"OSCAR","gene_name":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]","synonyms":null,"biotype":"protein_coding","ncbi_id":"126014","summary":"Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]","start":54094681,"end":54102740,"strand":-1,"description":"osteoclast associated, immunoglobulin-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]"}, {"versioned_ensembl_gene_id":"ENSG00000273496.1","gene_symbol":"AC011841.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":99351,"end":104855,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000243959.3","gene_symbol":"RN7SL684P","gene_name":"RNA, 7SL, cytoplasmic 684, pseudogene [Source:HGNC Symbol;Acc:HGNC:46700]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479472","summary":null,"start":176547433,"end":176547726,"strand":-1,"description":"RNA, 7SL, cytoplasmic 684, pseudogene [Source:HGNC Symbol;Acc:HGNC:46700]"}, {"versioned_ensembl_gene_id":"ENSG00000199773.1","gene_symbol":"RNU1-76P","gene_name":"RNA, U1 small nuclear 76, pseudogene [Source:HGNC Symbol;Acc:HGNC:48418]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481617","summary":null,"start":7980146,"end":7980304,"strand":1,"description":"RNA, U1 small nuclear 76, pseudogene [Source:HGNC Symbol;Acc:HGNC:48418]"}, {"versioned_ensembl_gene_id":"ENSG00000239102.1","gene_symbol":"RNU7-185P","gene_name":"RNA, U7 small nuclear 185 pseudogene [Source:HGNC Symbol;Acc:HGNC:45719]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479094","summary":null,"start":8797135,"end":8797194,"strand":1,"description":"RNA, U7 small nuclear 185 pseudogene [Source:HGNC Symbol;Acc:HGNC:45719]"}, {"versioned_ensembl_gene_id":"ENSG00000242014.3","gene_symbol":"RN7SL26P","gene_name":"RNA, 7SL, cytoplasmic 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46042]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479234","summary":null,"start":33540694,"end":33541000,"strand":1,"description":"RNA, 7SL, cytoplasmic 26, pseudogene [Source:HGNC Symbol;Acc:HGNC:46042]"}, {"versioned_ensembl_gene_id":"ENSG00000207196.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":70705167,"end":70705269,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275660.1","gene_symbol":"AC001228.1","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":2871423,"end":2871484,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000199530.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":82944738,"end":82944845,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252284.1","gene_symbol":"SNORA108","gene_name":"small nucleolar RNA, H/ACA box 108 [Source:HGNC Symbol;Acc:HGNC:51401]","synonyms":null,"biotype":"snoRNA","ncbi_id":"106635543","summary":null,"start":58600631,"end":58600698,"strand":1,"description":"small nucleolar RNA, H/ACA box 108 [Source:HGNC Symbol;Acc:HGNC:51401]"}, {"versioned_ensembl_gene_id":"ENSG00000277263.1","gene_symbol":"HLA-DRA","gene_name":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]","synonyms":"HLA-DRA1,HLA-DRA1","biotype":"protein_coding","ncbi_id":"3122","summary":"HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020]","start":32446915,"end":32452117,"strand":1,"description":"major histocompatibility complex, class II, DR alpha [Source:HGNC Symbol;Acc:HGNC:4947]"}, {"versioned_ensembl_gene_id":"ENSG00000240718.3","gene_symbol":"RN7SL851P","gene_name":"RNA, 7SL, cytoplasmic 851, pseudogene [Source:HGNC Symbol;Acc:HGNC:46867]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480537","summary":null,"start":6047721,"end":6048023,"strand":-1,"description":"RNA, 7SL, cytoplasmic 851, pseudogene [Source:HGNC Symbol;Acc:HGNC:46867]"}, {"versioned_ensembl_gene_id":"ENSG00000276988.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":128483907,"end":128484158,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199471.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":202914880,"end":202914980,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272533.1","gene_symbol":"SNORA28","gene_name":"small nucleolar RNA, H/ACA box 28 [Source:HGNC Symbol;Acc:HGNC:32618]","synonyms":"ACA28","biotype":"snoRNA","ncbi_id":"677811","summary":null,"start":103337849,"end":103337974,"strand":1,"description":"small nucleolar RNA, H/ACA box 28 [Source:HGNC Symbol;Acc:HGNC:32618]"}, {"versioned_ensembl_gene_id":"ENSG00000252385.1","gene_symbol":"RNU6-68P","gene_name":"RNA, U6 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:42558]","synonyms":"RNU6-68","biotype":"snRNA","ncbi_id":"100873772","summary":null,"start":46410454,"end":46410557,"strand":1,"description":"RNA, U6 small nuclear 68, pseudogene [Source:HGNC Symbol;Acc:HGNC:42558]"}, {"versioned_ensembl_gene_id":"ENSG00000251915.1","gene_symbol":"RNA5SP406","gene_name":"RNA, 5S ribosomal pseudogene 406 [Source:HGNC Symbol;Acc:HGNC:43306]","synonyms":"RN5S406","biotype":"rRNA","ncbi_id":"100873658","summary":null,"start":35734393,"end":35734504,"strand":1,"description":"RNA, 5S ribosomal pseudogene 406 [Source:HGNC Symbol;Acc:HGNC:43306]"}, {"versioned_ensembl_gene_id":"ENSG00000206686.1","gene_symbol":"RNU6-1036P","gene_name":"RNA, U6 small nuclear 1036, pseudogene [Source:HGNC Symbol;Acc:HGNC:47999]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480021","summary":null,"start":181007281,"end":181007384,"strand":1,"description":"RNA, U6 small nuclear 1036, pseudogene [Source:HGNC Symbol;Acc:HGNC:47999]"}, {"versioned_ensembl_gene_id":"ENSG00000243313.2","gene_symbol":"RN7SL285P","gene_name":"RNA, 7SL, cytoplasmic 285, pseudogene [Source:HGNC Symbol;Acc:HGNC:46301]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479326","summary":null,"start":37832922,"end":37833185,"strand":-1,"description":"RNA, 7SL, cytoplasmic 285, pseudogene [Source:HGNC Symbol;Acc:HGNC:46301]"}, {"versioned_ensembl_gene_id":"ENSG00000223273.1","gene_symbol":"RN7SKP172","gene_name":"RNA, 7SK small nuclear pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:45896]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480469","summary":null,"start":76315751,"end":76316048,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 172 [Source:HGNC Symbol;Acc:HGNC:45896]"}, {"versioned_ensembl_gene_id":"ENSG00000199483.1","gene_symbol":"RNU4-15P","gene_name":"RNA, U4 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:46951]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479565","summary":null,"start":83596444,"end":83596584,"strand":-1,"description":"RNA, U4 small nuclear 15, pseudogene [Source:HGNC Symbol;Acc:HGNC:46951]"}, {"versioned_ensembl_gene_id":"ENSG00000277234.1","gene_symbol":"RNU1-5P","gene_name":"RNA, U1 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:48304]","synonyms":"RNU1-5","biotype":"snRNA","ncbi_id":"107105261","summary":null,"start":16873708,"end":16873851,"strand":1,"description":"RNA, U1 small nuclear 5, pseudogene [Source:HGNC Symbol;Acc:HGNC:48304]"}, {"versioned_ensembl_gene_id":"ENSG00000199135.1","gene_symbol":"MIR101-1","gene_name":"microRNA 101-1 [Source:HGNC Symbol;Acc:HGNC:31488]","synonyms":"MIRN101-1,hsa-mir-101-1","biotype":"miRNA","ncbi_id":"406893","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65058434,"end":65058508,"strand":-1,"description":"microRNA 101-1 [Source:HGNC Symbol;Acc:HGNC:31488]"}, {"versioned_ensembl_gene_id":"ENSG00000199201.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":73192223,"end":73192325,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212378.1","gene_symbol":"SNORD78","gene_name":"Small nucleolar RNA SNORD78 [Source:RFAM;Acc:RF00592]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692198","summary":null,"start":72760534,"end":72760602,"strand":1,"description":"Small nucleolar RNA SNORD78 [Source:RFAM;Acc:RF00592]"}, {"versioned_ensembl_gene_id":"ENSG00000211543.2","gene_symbol":"MIR320B1","gene_name":"microRNA 320b-1 [Source:HGNC Symbol;Acc:HGNC:35247]","synonyms":"MIRN320B1,hsa-mir-320b-1","biotype":"miRNA","ncbi_id":"100302117","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116671749,"end":116671827,"strand":1,"description":"microRNA 320b-1 [Source:HGNC Symbol;Acc:HGNC:35247]"}, {"versioned_ensembl_gene_id":"ENSG00000223128.1","gene_symbol":"RN7SKP140","gene_name":"RNA, 7SK small nuclear pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:45864]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480366","summary":null,"start":21424758,"end":21425041,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 140 [Source:HGNC Symbol;Acc:HGNC:45864]"}, {"versioned_ensembl_gene_id":"ENSG00000264493.1","gene_symbol":"MIR4298","gene_name":"microRNA 4298 [Source:HGNC Symbol;Acc:HGNC:38313]","synonyms":"hsa-mir-4298","biotype":"miRNA","ncbi_id":"100423021","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1859464,"end":1859536,"strand":-1,"description":"microRNA 4298 [Source:HGNC Symbol;Acc:HGNC:38313]"}, {"versioned_ensembl_gene_id":"ENSG00000207994.1","gene_symbol":"MIR100","gene_name":"microRNA 100 [Source:HGNC Symbol;Acc:HGNC:31487]","synonyms":"MIRN100,hsa-mir-100","biotype":"miRNA","ncbi_id":"406892","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122152229,"end":122152308,"strand":-1,"description":"microRNA 100 [Source:HGNC Symbol;Acc:HGNC:31487]"}, {"versioned_ensembl_gene_id":"ENSG00000239908.3","gene_symbol":"RN7SL75P","gene_name":"RNA, 7SL, cytoplasmic 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:46091]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107063539","summary":null,"start":100102559,"end":100102839,"strand":1,"description":"RNA, 7SL, cytoplasmic 75, pseudogene [Source:HGNC Symbol;Acc:HGNC:46091]"}, {"versioned_ensembl_gene_id":"ENSG00000266043.1","gene_symbol":"MIR3649","gene_name":"microRNA 3649 [Source:HGNC Symbol;Acc:HGNC:38948]","synonyms":"hsa-mir-3649","biotype":"miRNA","ncbi_id":"100500816","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1660315,"end":1660380,"strand":-1,"description":"microRNA 3649 [Source:HGNC Symbol;Acc:HGNC:38948]"}, {"versioned_ensembl_gene_id":"ENSG00000265882.2","gene_symbol":"RN7SL73P","gene_name":"RNA, 7SL, cytoplasmic 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:46089]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479250","summary":null,"start":195553792,"end":195554043,"strand":1,"description":"RNA, 7SL, cytoplasmic 73, pseudogene [Source:HGNC Symbol;Acc:HGNC:46089]"}, {"versioned_ensembl_gene_id":"ENSG00000283614.1","gene_symbol":"MIR7973-2","gene_name":"microRNA 7973-2 [Source:HGNC Symbol;Acc:HGNC:50080]","synonyms":"hsa-mir-7973-2","biotype":"miRNA","ncbi_id":"102465855","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51314032,"end":51314107,"strand":-1,"description":"microRNA 7973-2 [Source:HGNC Symbol;Acc:HGNC:50080]"}, {"versioned_ensembl_gene_id":"ENSG00000221355.1","gene_symbol":"MIR1288","gene_name":"microRNA 1288 [Source:HGNC Symbol;Acc:HGNC:35363]","synonyms":"MIRN1288,hsa-mir-1288","biotype":"miRNA","ncbi_id":"100302124","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16282014,"end":16282088,"strand":1,"description":"microRNA 1288 [Source:HGNC Symbol;Acc:HGNC:35363]"}, {"versioned_ensembl_gene_id":"ENSG00000199929.1","gene_symbol":"RNA5SP405","gene_name":"RNA, 5S ribosomal pseudogene 405 [Source:HGNC Symbol;Acc:HGNC:43305]","synonyms":"RN5S405","biotype":"rRNA","ncbi_id":"100873657","summary":null,"start":26028912,"end":26029025,"strand":1,"description":"RNA, 5S ribosomal pseudogene 405 [Source:HGNC Symbol;Acc:HGNC:43305]"}, {"versioned_ensembl_gene_id":"ENSG00000273627.1","gene_symbol":"MIR4726","gene_name":"microRNA 4726 [Source:HGNC Symbol;Acc:HGNC:41722]","synonyms":"hsa-mir-4726","biotype":"miRNA","ncbi_id":"100616153","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":38719691,"end":38719748,"strand":1,"description":"microRNA 4726 [Source:HGNC Symbol;Acc:HGNC:41722]"}, {"versioned_ensembl_gene_id":"ENSG00000223060.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56105416,"end":56105510,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284144.1","gene_symbol":"MIR6866","gene_name":"microRNA 6866 [Source:HGNC Symbol;Acc:HGNC:49932]","synonyms":"hsa-mir-6866","biotype":"miRNA","ncbi_id":"102466986","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40161933,"end":40162001,"strand":1,"description":"microRNA 6866 [Source:HGNC Symbol;Acc:HGNC:49932]"}, {"versioned_ensembl_gene_id":"ENSG00000283927.1","gene_symbol":"MIR133A1","gene_name":"microRNA 133a-1 [Source:HGNC Symbol;Acc:HGNC:31517]","synonyms":"MIRN133A1,hsa-mir-133a-1","biotype":"miRNA","ncbi_id":"406922","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21825698,"end":21825785,"strand":-1,"description":"microRNA 133a-1 [Source:HGNC Symbol;Acc:HGNC:31517]"}, {"versioned_ensembl_gene_id":"ENSG00000252474.1","gene_symbol":"RNU6-539P","gene_name":"RNA, U6 small nuclear 539, pseudogene [Source:HGNC Symbol;Acc:HGNC:47502]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481351","summary":null,"start":49839725,"end":49839827,"strand":1,"description":"RNA, U6 small nuclear 539, pseudogene [Source:HGNC Symbol;Acc:HGNC:47502]"}, {"versioned_ensembl_gene_id":"ENSG00000265390.1","gene_symbol":"MIR4999","gene_name":"microRNA 4999 [Source:HGNC Symbol;Acc:HGNC:43494]","synonyms":"hsa-mir-4999","biotype":"miRNA","ncbi_id":"100847049","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8389290,"end":8389380,"strand":-1,"description":"microRNA 4999 [Source:HGNC Symbol;Acc:HGNC:43494]"}, {"versioned_ensembl_gene_id":"ENSG00000212224.1","gene_symbol":"SNORA26","gene_name":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]","synonyms":"HBI-6","biotype":"snoRNA","ncbi_id":"677810","summary":null,"start":41712479,"end":41712600,"strand":-1,"description":"Small nucleolar RNA SNORA26 [Source:RFAM;Acc:RF00568]"}, {"versioned_ensembl_gene_id":"ENSG00000274542.1","gene_symbol":"AC243734.1","gene_name":"neuronal acetylcholine receptor subunit alpha-7 isoform 2 precursor [Source:RefSeq peptide;Acc:NP_001177384]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":32181324,"end":32319966,"strand":1,"description":"neuronal acetylcholine receptor subunit alpha-7 isoform 2 precursor [Source:RefSeq peptide;Acc:NP_001177384]"}, {"versioned_ensembl_gene_id":"ENSG00000274417.1","gene_symbol":"MIR6515","gene_name":"microRNA 6515 [Source:HGNC Symbol;Acc:HGNC:50227]","synonyms":"hsa-mir-6515","biotype":"miRNA","ncbi_id":"102466659","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12940484,"end":12940540,"strand":1,"description":"microRNA 6515 [Source:HGNC Symbol;Acc:HGNC:50227]"}, {"versioned_ensembl_gene_id":"ENSG00000200095.1","gene_symbol":"RNU6-181P","gene_name":"RNA, U6 small nuclear 181, pseudogene [Source:HGNC Symbol;Acc:HGNC:47144]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480559","summary":null,"start":100560686,"end":100560792,"strand":-1,"description":"RNA, U6 small nuclear 181, pseudogene [Source:HGNC Symbol;Acc:HGNC:47144]"}, {"versioned_ensembl_gene_id":"ENSG00000207821.1","gene_symbol":"MIR640","gene_name":"microRNA 640 [Source:HGNC Symbol;Acc:HGNC:32896]","synonyms":"MIRN640,hsa-mir-640","biotype":"miRNA","ncbi_id":"693225","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19435063,"end":19435158,"strand":1,"description":"microRNA 640 [Source:HGNC Symbol;Acc:HGNC:32896]"}, {"versioned_ensembl_gene_id":"ENSG00000206808.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":33171381,"end":33171490,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207631.1","gene_symbol":"MIR641","gene_name":"microRNA 641 [Source:HGNC Symbol;Acc:HGNC:32897]","synonyms":"MIRN641,hsa-mir-641","biotype":"miRNA","ncbi_id":"693226","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":40282543,"end":40282641,"strand":-1,"description":"microRNA 641 [Source:HGNC Symbol;Acc:HGNC:32897]"}, {"versioned_ensembl_gene_id":"ENSG00000265892.2","gene_symbol":"RN7SL311P","gene_name":"RNA, 7SL, cytoplasmic 311, pseudogene [Source:HGNC Symbol;Acc:HGNC:46327]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481755","summary":null,"start":139185441,"end":139185746,"strand":1,"description":"RNA, 7SL, cytoplasmic 311, pseudogene [Source:HGNC Symbol;Acc:HGNC:46327]"}, {"versioned_ensembl_gene_id":"ENSG00000273942.1","gene_symbol":"RMST_2","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 2 [Source:RFAM;Acc:RF01963]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97492462,"end":97492597,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 2 [Source:RFAM;Acc:RF01963]"}, {"versioned_ensembl_gene_id":"ENSG00000207082.1","gene_symbol":"RNU6-171P","gene_name":"RNA, U6 small nuclear 171, pseudogene [Source:HGNC Symbol;Acc:HGNC:47134]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481230","summary":null,"start":164639565,"end":164639671,"strand":1,"description":"RNA, U6 small nuclear 171, pseudogene [Source:HGNC Symbol;Acc:HGNC:47134]"}, {"versioned_ensembl_gene_id":"ENSG00000206729.1","gene_symbol":"RNU6-1126P","gene_name":"RNA, U6 small nuclear 1126, pseudogene [Source:HGNC Symbol;Acc:HGNC:48089]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481535","summary":null,"start":55789368,"end":55789474,"strand":1,"description":"RNA, U6 small nuclear 1126, pseudogene [Source:HGNC Symbol;Acc:HGNC:48089]"}, {"versioned_ensembl_gene_id":"ENSG00000278783.1","gene_symbol":"MIR6071","gene_name":"microRNA 6071 [Source:HGNC Symbol;Acc:HGNC:50229]","synonyms":"hsa-mir-6071","biotype":"miRNA","ncbi_id":"102466516","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85783600,"end":85783677,"strand":-1,"description":"microRNA 6071 [Source:HGNC Symbol;Acc:HGNC:50229]"}, {"versioned_ensembl_gene_id":"ENSG00000199672.1","gene_symbol":"RNU4-21P","gene_name":"RNA, U4 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:46957]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481178","summary":null,"start":229535064,"end":229535189,"strand":-1,"description":"RNA, U4 small nuclear 21, pseudogene [Source:HGNC Symbol;Acc:HGNC:46957]"}, {"versioned_ensembl_gene_id":"ENSG00000265965.1","gene_symbol":"MIR4266","gene_name":"microRNA 4266 [Source:HGNC Symbol;Acc:HGNC:38175]","synonyms":"hsa-mir-4266","biotype":"miRNA","ncbi_id":"100423027","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":109313571,"end":109313625,"strand":-1,"description":"microRNA 4266 [Source:HGNC Symbol;Acc:HGNC:38175]"}, {"versioned_ensembl_gene_id":"ENSG00000278420.1","gene_symbol":"MIR6819","gene_name":"microRNA 6819 [Source:HGNC Symbol;Acc:HGNC:50155]","synonyms":"hsa-mir-6819","biotype":"miRNA","ncbi_id":"102465491","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36286847,"end":36286907,"strand":-1,"description":"microRNA 6819 [Source:HGNC Symbol;Acc:HGNC:50155]"}, {"versioned_ensembl_gene_id":"ENSG00000277890.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":34890,"end":34996,"strand":1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000263631.1","gene_symbol":"MIR378D1","gene_name":"microRNA 378d-1 [Source:HGNC Symbol;Acc:HGNC:41550]","synonyms":"hsa-mir-378d-1","biotype":"miRNA","ncbi_id":"100616201","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5923275,"end":5923328,"strand":-1,"description":"microRNA 378d-1 [Source:HGNC Symbol;Acc:HGNC:41550]"}, {"versioned_ensembl_gene_id":"ENSG00000221518.1","gene_symbol":"RNU6ATAC16P","gene_name":"RNA, U6atac small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46915]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479550","summary":null,"start":52560570,"end":52560707,"strand":1,"description":"RNA, U6atac small nuclear 16, pseudogene [Source:HGNC Symbol;Acc:HGNC:46915]"}, {"versioned_ensembl_gene_id":"ENSG00000284253.1","gene_symbol":"MIR1973","gene_name":"microRNA 1973 [Source:HGNC Symbol;Acc:HGNC:37061]","synonyms":"hsa-mir-1973","biotype":"miRNA","ncbi_id":"100302290","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":116299725,"end":116299768,"strand":1,"description":"microRNA 1973 [Source:HGNC Symbol;Acc:HGNC:37061]"}, {"versioned_ensembl_gene_id":"ENSG00000200344.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":7982881,"end":7982983,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276350.1","gene_symbol":"MIR6858","gene_name":"microRNA 6858 [Source:HGNC Symbol;Acc:HGNC:50250]","synonyms":"hsa-mir-6858","biotype":"miRNA","ncbi_id":"102465517","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154450320,"end":154450386,"strand":1,"description":"microRNA 6858 [Source:HGNC Symbol;Acc:HGNC:50250]"}, {"versioned_ensembl_gene_id":"ENSG00000199223.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6572956,"end":6573057,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263537.2","gene_symbol":"RN7SL387P","gene_name":"RNA, 7SL, cytoplasmic 387, pseudogene [Source:HGNC Symbol;Acc:HGNC:46403]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481029","summary":null,"start":110625645,"end":110625917,"strand":-1,"description":"RNA, 7SL, cytoplasmic 387, pseudogene [Source:HGNC Symbol;Acc:HGNC:46403]"}, {"versioned_ensembl_gene_id":"ENSG00000201440.1","gene_symbol":"RNA5SP515","gene_name":"RNA, 5S ribosomal pseudogene 515 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252654.1","gene_symbol":"RNU7-6P","gene_name":"RNA, U7 small nuclear 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:34102]","synonyms":"U7.6","biotype":"snRNA","ncbi_id":"100147749","summary":null,"start":51904969,"end":51905030,"strand":1,"description":"RNA, U7 small nuclear 6 pseudogene [Source:HGNC Symbol;Acc:HGNC:34102]"}, {"versioned_ensembl_gene_id":"ENSG00000201763.1","gene_symbol":"RNA5SP267","gene_name":"RNA, 5S ribosomal pseudogene 267 [Source:HGNC Symbol;Acc:HGNC:43167]","synonyms":"RN5S267","biotype":"rRNA","ncbi_id":"100873520","summary":null,"start":59455885,"end":59456010,"strand":1,"description":"RNA, 5S ribosomal pseudogene 267 [Source:HGNC Symbol;Acc:HGNC:43167]"}, {"versioned_ensembl_gene_id":"ENSG00000207518.1","gene_symbol":"RNU6-59P","gene_name":"RNA, U6 small nuclear 59, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000277828.1","gene_symbol":"AL137067.2","gene_name":null,"synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99357827,"end":99357957,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000277370.1","gene_symbol":"SNORD49A","gene_name":"small nucleolar RNA, C/D box 49A [Source:HGNC Symbol;Acc:HGNC:10189]","synonyms":"U49A,U49,RNU49","biotype":"snoRNA","ncbi_id":"26800","summary":null,"start":16440036,"end":16440106,"strand":1,"description":"small nucleolar RNA, C/D box 49A [Source:HGNC Symbol;Acc:HGNC:10189]"}, {"versioned_ensembl_gene_id":"ENSG00000274906.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":148436777,"end":148437045,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000201654.1","gene_symbol":"RNU6-7","gene_name":"RNA, U6 small nuclear 7 [Source:HGNC Symbol;Acc:HGNC:34284]","synonyms":"U6-7","biotype":"snRNA","ncbi_id":"101954275","summary":null,"start":32202045,"end":32202151,"strand":1,"description":"RNA, U6 small nuclear 7 [Source:HGNC Symbol;Acc:HGNC:34284]"}, {"versioned_ensembl_gene_id":"ENSG00000201482.1","gene_symbol":"SNORD115-17","gene_name":"small nucleolar RNA, C/D box 115-17 [Source:HGNC Symbol;Acc:HGNC:33036]","synonyms":"HBII-52-17","biotype":"snoRNA","ncbi_id":"100033455","summary":null,"start":25201323,"end":25201404,"strand":1,"description":"small nucleolar RNA, C/D box 115-17 [Source:HGNC Symbol;Acc:HGNC:33036]"}, {"versioned_ensembl_gene_id":"ENSG00000207458.1","gene_symbol":"RNY3P9","gene_name":"RNA, Ro-associated Y3 pseudogene 9 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000277108.1","gene_symbol":"SNORD49B","gene_name":"small nucleolar RNA, C/D box 49B [Source:HGNC Symbol;Acc:HGNC:32721]","synonyms":"U49B","biotype":"snoRNA","ncbi_id":"692087","summary":null,"start":16439505,"end":16439576,"strand":1,"description":"small nucleolar RNA, C/D box 49B [Source:HGNC Symbol;Acc:HGNC:32721]"}, {"versioned_ensembl_gene_id":"ENSG00000199666.2","gene_symbol":"SNORD3G","gene_name":"small nucleolar RNA, C/D box 3G [Source:HGNC Symbol;Acc:HGNC:52240]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109616984","summary":null,"start":90657750,"end":90657964,"strand":1,"description":"small nucleolar RNA, C/D box 3G [Source:HGNC Symbol;Acc:HGNC:52240]"}, {"versioned_ensembl_gene_id":"ENSG00000283712.1","gene_symbol":"MIR6727","gene_name":"microRNA 6727 [Source:HGNC Symbol;Acc:HGNC:50171]","synonyms":"hsa-mir-6727","biotype":"miRNA","ncbi_id":"102465435","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1312502,"end":1312566,"strand":-1,"description":"microRNA 6727 [Source:HGNC Symbol;Acc:HGNC:50171]"}, {"versioned_ensembl_gene_id":"ENSG00000244107.3","gene_symbol":"RN7SL250P","gene_name":"RNA, 7SL, cytoplasmic 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:46266]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479313","summary":null,"start":54420468,"end":54420725,"strand":1,"description":"RNA, 7SL, cytoplasmic 250, pseudogene [Source:HGNC Symbol;Acc:HGNC:46266]"}, {"versioned_ensembl_gene_id":"ENSG00000206969.1","gene_symbol":"RNU6-1316P","gene_name":"RNA, U6 small nuclear 1316, pseudogene [Source:HGNC Symbol;Acc:HGNC:48279]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480140","summary":null,"start":102865856,"end":102865963,"strand":1,"description":"RNA, U6 small nuclear 1316, pseudogene [Source:HGNC Symbol;Acc:HGNC:48279]"}, {"versioned_ensembl_gene_id":"ENSG00000283749.1","gene_symbol":"MIR4781","gene_name":"microRNA 4781 [Source:HGNC Symbol;Acc:HGNC:41769]","synonyms":"hsa-mir-4781","biotype":"miRNA","ncbi_id":"100616315","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54054079,"end":54054154,"strand":1,"description":"microRNA 4781 [Source:HGNC Symbol;Acc:HGNC:41769]"}, {"versioned_ensembl_gene_id":"ENSG00000222524.1","gene_symbol":"RN7SKP109","gene_name":"RNA, 7SK small nuclear pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:45833]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479143","summary":null,"start":55737285,"end":55737600,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 109 [Source:HGNC Symbol;Acc:HGNC:45833]"}, {"versioned_ensembl_gene_id":"ENSG00000199704.1","gene_symbol":"SNORD115-29","gene_name":"small nucleolar RNA, C/D box 115-29 [Source:HGNC Symbol;Acc:HGNC:33048]","synonyms":"HBII-52-29","biotype":"snoRNA","ncbi_id":"100033803","summary":null,"start":25223246,"end":25223327,"strand":1,"description":"small nucleolar RNA, C/D box 115-29 [Source:HGNC Symbol;Acc:HGNC:33048]"}, {"versioned_ensembl_gene_id":"ENSG00000283701.1","gene_symbol":"MIR555","gene_name":"microRNA 555 [Source:HGNC Symbol;Acc:HGNC:32811]","synonyms":"MIRN555,hsa-mir-555","biotype":"miRNA","ncbi_id":"693140","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":155346350,"end":155346445,"strand":-1,"description":"microRNA 555 [Source:HGNC Symbol;Acc:HGNC:32811]"}, {"versioned_ensembl_gene_id":"ENSG00000238765.1","gene_symbol":"RNA5SP57","gene_name":"RNA, 5S ribosomal pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:42834]","synonyms":"RNA5SP58,RN5S58,RN5S57","biotype":"rRNA","ncbi_id":"106480754","summary":null,"start":148193716,"end":148193838,"strand":1,"description":"RNA, 5S ribosomal pseudogene 57 [Source:HGNC Symbol;Acc:HGNC:42834]"}, {"versioned_ensembl_gene_id":"ENSG00000199603.1","gene_symbol":"RNU6-951P","gene_name":"RNA, U6 small nuclear 951, pseudogene [Source:HGNC Symbol;Acc:HGNC:47914]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481480","summary":null,"start":38147415,"end":38147521,"strand":1,"description":"RNA, U6 small nuclear 951, pseudogene [Source:HGNC Symbol;Acc:HGNC:47914]"}, {"versioned_ensembl_gene_id":"ENSG00000283936.1","gene_symbol":"MIR3658","gene_name":"microRNA 3658 [Source:HGNC Symbol;Acc:HGNC:38963]","synonyms":"hsa-mir-3658","biotype":"miRNA","ncbi_id":"100500832","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":165907921,"end":165907976,"strand":1,"description":"microRNA 3658 [Source:HGNC Symbol;Acc:HGNC:38963]"}, {"versioned_ensembl_gene_id":"ENSG00000251865.1","gene_symbol":"RNU6-518P","gene_name":"RNA, U6 small nuclear 518, pseudogene [Source:HGNC Symbol;Acc:HGNC:47481]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481344","summary":null,"start":58835899,"end":58835994,"strand":1,"description":"RNA, U6 small nuclear 518, pseudogene [Source:HGNC Symbol;Acc:HGNC:47481]"}, {"versioned_ensembl_gene_id":"ENSG00000201945.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":121107043,"end":121107174,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000283844.1","gene_symbol":"MIR214","gene_name":"microRNA 214 [Source:HGNC Symbol;Acc:HGNC:31591]","synonyms":"MIRN214,hsa-mir-214","biotype":"miRNA","ncbi_id":"406996","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":172138798,"end":172138907,"strand":-1,"description":"microRNA 214 [Source:HGNC Symbol;Acc:HGNC:31591]"}, {"versioned_ensembl_gene_id":"ENSG00000252228.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30132805,"end":30132966,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000284311.1","gene_symbol":"MIR6742","gene_name":"microRNA 6742 [Source:HGNC Symbol;Acc:HGNC:50090]","synonyms":"hsa-mir-6742","biotype":"miRNA","ncbi_id":"102465444","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":228397048,"end":228397109,"strand":-1,"description":"microRNA 6742 [Source:HGNC Symbol;Acc:HGNC:50090]"}, {"versioned_ensembl_gene_id":"ENSG00000278069.1","gene_symbol":"MIR6072","gene_name":"microRNA 6072 [Source:HGNC Symbol;Acc:HGNC:50144]","synonyms":"hsa-mir-6072","biotype":"miRNA","ncbi_id":"102465944","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2076019,"end":2076089,"strand":-1,"description":"microRNA 6072 [Source:HGNC Symbol;Acc:HGNC:50144]"}, {"versioned_ensembl_gene_id":"ENSG00000206869.1","gene_symbol":"SNORA70F","gene_name":"small nucleolar RNA, H/ACA box 70F [Source:HGNC Symbol;Acc:HGNC:34358]","synonyms":"U70F","biotype":"snoRNA","ncbi_id":"100337591","summary":null,"start":164687643,"end":164687777,"strand":-1,"description":"small nucleolar RNA, H/ACA box 70F [Source:HGNC Symbol;Acc:HGNC:34358]"}, {"versioned_ensembl_gene_id":"ENSG00000207221.1","gene_symbol":"SNORA70E","gene_name":"small nucleolar RNA, H/ACA box 70E [Source:HGNC Symbol;Acc:HGNC:34357]","synonyms":"U70E","biotype":"snoRNA","ncbi_id":"100379250","summary":null,"start":83041464,"end":83041598,"strand":-1,"description":"small nucleolar RNA, H/ACA box 70E [Source:HGNC Symbol;Acc:HGNC:34357]"}, {"versioned_ensembl_gene_id":"ENSG00000274809.1","gene_symbol":"MIR6078","gene_name":"microRNA 6078 [Source:HGNC Symbol;Acc:HGNC:50136]","synonyms":"hsa-mir-6078","biotype":"miRNA","ncbi_id":"102464829","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3991160,"end":3991259,"strand":1,"description":"microRNA 6078 [Source:HGNC Symbol;Acc:HGNC:50136]"}, {"versioned_ensembl_gene_id":"ENSG00000276965.1","gene_symbol":"TUG1_3","gene_name":"Taurine upregulated gene 1 conserved region 3 [Source:RFAM;Acc:RF01891]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30972857,"end":30973093,"strand":1,"description":"Taurine upregulated gene 1 conserved region 3 [Source:RFAM;Acc:RF01891]"}, {"versioned_ensembl_gene_id":"ENSG00000277395.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":36491571,"end":36491694,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000221331.1","gene_symbol":"MIR548Q","gene_name":"microRNA 548q [Source:HGNC Symbol;Acc:HGNC:37312]","synonyms":"hsa-mir-548q","biotype":"miRNA","ncbi_id":"100313841","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12725254,"end":12725353,"strand":-1,"description":"microRNA 548q [Source:HGNC Symbol;Acc:HGNC:37312]"}, {"versioned_ensembl_gene_id":"ENSG00000212140.1","gene_symbol":"RNU6-1320P","gene_name":"RNA, U6 small nuclear 1320, pseudogene [Source:HGNC Symbol;Acc:HGNC:48283]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480659","summary":null,"start":94846533,"end":94846639,"strand":-1,"description":"RNA, U6 small nuclear 1320, pseudogene [Source:HGNC Symbol;Acc:HGNC:48283]"}, {"versioned_ensembl_gene_id":"ENSG00000221371.1","gene_symbol":"MIR1265","gene_name":"microRNA 1265 [Source:HGNC Symbol;Acc:HGNC:35332]","synonyms":"MIRN1265,hsa-mir-1265","biotype":"miRNA","ncbi_id":"100302116","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14436576,"end":14436661,"strand":1,"description":"microRNA 1265 [Source:HGNC Symbol;Acc:HGNC:35332]"}, {"versioned_ensembl_gene_id":"ENSG00000252886.1","gene_symbol":"RN7SKP197","gene_name":"RNA, 7SK small nuclear pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:45921]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480894","summary":null,"start":119631090,"end":119631386,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 197 [Source:HGNC Symbol;Acc:HGNC:45921]"}, {"versioned_ensembl_gene_id":"ENSG00000207571.1","gene_symbol":"MIR615","gene_name":"microRNA 615 [Source:HGNC Symbol;Acc:HGNC:32871]","synonyms":"MIRN615,hsa-mir-615","biotype":"miRNA","ncbi_id":"693200","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54033950,"end":54034045,"strand":1,"description":"microRNA 615 [Source:HGNC Symbol;Acc:HGNC:32871]"}, {"versioned_ensembl_gene_id":"ENSG00000201564.1","gene_symbol":"RN7SKP50","gene_name":"RNA, 7SK small nuclear pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45774]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480459","summary":null,"start":9680924,"end":9681238,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:45774]"}, {"versioned_ensembl_gene_id":"ENSG00000207352.1","gene_symbol":"RNU6-540P","gene_name":"RNA, U6 small nuclear 540, pseudogene [Source:HGNC Symbol;Acc:HGNC:47503]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479806","summary":null,"start":65604661,"end":65604761,"strand":-1,"description":"RNA, U6 small nuclear 540, pseudogene [Source:HGNC Symbol;Acc:HGNC:47503]"}, {"versioned_ensembl_gene_id":"ENSG00000199593.1","gene_symbol":"SNORD114-14","gene_name":"small nucleolar RNA, C/D box 114-14 [Source:HGNC Symbol;Acc:HGNC:33002]","synonyms":"14q(II-14)","biotype":"snoRNA","ncbi_id":"767592","summary":null,"start":100972103,"end":100972177,"strand":1,"description":"small nucleolar RNA, C/D box 114-14 [Source:HGNC Symbol;Acc:HGNC:33002]"}, {"versioned_ensembl_gene_id":"ENSG00000266099.1","gene_symbol":"MIR5700","gene_name":"microRNA 5700 [Source:HGNC Symbol;Acc:HGNC:43521]","synonyms":"hsa-mir-5700","biotype":"miRNA","ncbi_id":"100847031","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94561789,"end":94561859,"strand":1,"description":"microRNA 5700 [Source:HGNC Symbol;Acc:HGNC:43521]"}, {"versioned_ensembl_gene_id":"ENSG00000238917.1","gene_symbol":"SNORD10","gene_name":"small nucleolar RNA, C/D box 10 [Source:HGNC Symbol;Acc:HGNC:32706]","synonyms":"mgU6-77","biotype":"snoRNA","ncbi_id":"652966","summary":null,"start":7576811,"end":7576952,"strand":1,"description":"small nucleolar RNA, C/D box 10 [Source:HGNC Symbol;Acc:HGNC:32706]"}, {"versioned_ensembl_gene_id":"ENSG00000200169.1","gene_symbol":"RNU5D-1","gene_name":"RNA, U5D small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10214]","synonyms":"RNU5D,U5DS,U5DL","biotype":"snRNA","ncbi_id":"26830","summary":null,"start":44731055,"end":44731170,"strand":-1,"description":"RNA, U5D small nuclear 1 [Source:HGNC Symbol;Acc:HGNC:10214]"}, {"versioned_ensembl_gene_id":"ENSG00000199107.3","gene_symbol":"MIR409","gene_name":"microRNA 409 [Source:HGNC Symbol;Acc:HGNC:32055]","synonyms":"MIRN409,hsa-mir-409","biotype":"miRNA","ncbi_id":"574413","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101065300,"end":101065378,"strand":1,"description":"microRNA 409 [Source:HGNC Symbol;Acc:HGNC:32055]"}, {"versioned_ensembl_gene_id":"ENSG00000212189.1","gene_symbol":"RNU6-328P","gene_name":"RNA, U6 small nuclear 328, pseudogene [Source:HGNC Symbol;Acc:HGNC:47291]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479711","summary":null,"start":7004007,"end":7004112,"strand":-1,"description":"RNA, U6 small nuclear 328, pseudogene [Source:HGNC Symbol;Acc:HGNC:47291]"}, {"versioned_ensembl_gene_id":"ENSG00000264733.1","gene_symbol":"MIR4718","gene_name":"microRNA 4718 [Source:HGNC Symbol;Acc:HGNC:41900]","synonyms":"hsa-mir-4718","biotype":"miRNA","ncbi_id":"100616195","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12720321,"end":12720371,"strand":1,"description":"microRNA 4718 [Source:HGNC Symbol;Acc:HGNC:41900]"}, {"versioned_ensembl_gene_id":"ENSG00000212589.1","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":113820459,"end":113820590,"strand":1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000251789.2","gene_symbol":"RNU4-57P","gene_name":"RNA, U4 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46993]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479584","summary":null,"start":223373822,"end":223373956,"strand":1,"description":"RNA, U4 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:46993]"}, {"versioned_ensembl_gene_id":"ENSG00000275259.1","gene_symbol":"MIR6511A1","gene_name":"microRNA 6511a-1 [Source:HGNC Symbol;Acc:HGNC:50119]","synonyms":"hsa-mir-6511a-1","biotype":"miRNA","ncbi_id":"102466268","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14925937,"end":14926003,"strand":1,"description":"microRNA 6511a-1 [Source:HGNC Symbol;Acc:HGNC:50119]"}, {"versioned_ensembl_gene_id":"ENSG00000201910.1","gene_symbol":"RNU1-140P","gene_name":"RNA, U1 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48482]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480669","summary":null,"start":104098874,"end":104099038,"strand":1,"description":"RNA, U1 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:48482]"}, {"versioned_ensembl_gene_id":"ENSG00000266276.3","gene_symbol":"MIR4743","gene_name":"microRNA 4743 [Source:HGNC Symbol;Acc:HGNC:41894]","synonyms":"hsa-mir-4743","biotype":"miRNA","ncbi_id":"100616366","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48670600,"end":48670668,"strand":1,"description":"microRNA 4743 [Source:HGNC Symbol;Acc:HGNC:41894]"}, {"versioned_ensembl_gene_id":"ENSG00000206725.1","gene_symbol":"RNU6-1027P","gene_name":"RNA, U6 small nuclear 1027, pseudogene [Source:HGNC Symbol;Acc:HGNC:47990]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481505","summary":null,"start":229973315,"end":229973421,"strand":1,"description":"RNA, U6 small nuclear 1027, pseudogene [Source:HGNC Symbol;Acc:HGNC:47990]"}, {"versioned_ensembl_gene_id":"ENSG00000222582.1","gene_symbol":"RNU2-66P","gene_name":"RNA, U2 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:48559]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481655","summary":null,"start":154787118,"end":154787278,"strand":1,"description":"RNA, U2 small nuclear 66, pseudogene [Source:HGNC Symbol;Acc:HGNC:48559]"}, {"versioned_ensembl_gene_id":"ENSG00000252259.1","gene_symbol":"RNA5SP49","gene_name":"RNA, 5S ribosomal pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:42825]","synonyms":"RN5S49","biotype":"rRNA","ncbi_id":"100873288","summary":null,"start":63186336,"end":63186450,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 49 [Source:HGNC Symbol;Acc:HGNC:42825]"}, {"versioned_ensembl_gene_id":"ENSG00000283330.1","gene_symbol":"MIR518D","gene_name":"microRNA 518d [Source:HGNC Symbol;Acc:HGNC:32121]","synonyms":"MIRN518D,hsa-mir-518d","biotype":"miRNA","ncbi_id":"574489","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53734877,"end":53734963,"strand":1,"description":"microRNA 518d [Source:HGNC Symbol;Acc:HGNC:32121]"}, {"versioned_ensembl_gene_id":"ENSG00000201919.1","gene_symbol":"RNU6-1022P","gene_name":"RNA, U6 small nuclear 1022, pseudogene [Source:HGNC Symbol;Acc:HGNC:47985]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480016","summary":null,"start":21987816,"end":21987919,"strand":1,"description":"RNA, U6 small nuclear 1022, pseudogene [Source:HGNC Symbol;Acc:HGNC:47985]"}, {"versioned_ensembl_gene_id":"ENSG00000277636.1","gene_symbol":"MIR8061","gene_name":"microRNA 8061 [Source:HGNC Symbol;Acc:HGNC:50077]","synonyms":"hsa-mir-8061","biotype":"miRNA","ncbi_id":"102466251","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54645309,"end":54645383,"strand":1,"description":"microRNA 8061 [Source:HGNC Symbol;Acc:HGNC:50077]"}, {"versioned_ensembl_gene_id":"ENSG00000276186.1","gene_symbol":"RNU6-1025P","gene_name":"RNA, U6 small nuclear 1025, pseudogene [Source:HGNC Symbol;Acc:HGNC:47988]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480018","summary":null,"start":948421,"end":948524,"strand":1,"description":"RNA, U6 small nuclear 1025, pseudogene [Source:HGNC Symbol;Acc:HGNC:47988]"}, {"versioned_ensembl_gene_id":"ENSG00000252267.1","gene_symbol":"RNA5SP495","gene_name":"RNA, 5S ribosomal pseudogene 495 [Source:HGNC Symbol;Acc:HGNC:43395]","synonyms":"RN5S495","biotype":"rRNA","ncbi_id":"100873737","summary":null,"start":26390667,"end":26390776,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 495 [Source:HGNC Symbol;Acc:HGNC:43395]"}, {"versioned_ensembl_gene_id":"ENSG00000284481.1","gene_symbol":"MIR1292","gene_name":"microRNA 1292 [Source:HGNC Symbol;Acc:HGNC:35364]","synonyms":"MIRN1292,hsa-mir-1292","biotype":"miRNA","ncbi_id":"100302138","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2652777,"end":2652842,"strand":1,"description":"microRNA 1292 [Source:HGNC Symbol;Acc:HGNC:35364]"}, {"versioned_ensembl_gene_id":"ENSG00000264354.1","gene_symbol":"MIR3134","gene_name":"microRNA 3134 [Source:HGNC Symbol;Acc:HGNC:38254]","synonyms":"hsa-mir-3134","biotype":"miRNA","ncbi_id":"100422990","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":15697298,"end":15697371,"strand":-1,"description":"microRNA 3134 [Source:HGNC Symbol;Acc:HGNC:38254]"}, {"versioned_ensembl_gene_id":"ENSG00000199953.1","gene_symbol":"RNA5SP443","gene_name":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]","synonyms":"RN5S443","biotype":"rRNA","ncbi_id":"106481745","summary":null,"start":45327366,"end":45327497,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]"}, {"versioned_ensembl_gene_id":"ENSG00000221263.1","gene_symbol":"MIR548P","gene_name":"microRNA 548p [Source:HGNC Symbol;Acc:HGNC:35351]","synonyms":"MIRN548P,hsa-mir-548p","biotype":"miRNA","ncbi_id":"100302288","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100816482,"end":100816565,"strand":-1,"description":"microRNA 548p [Source:HGNC Symbol;Acc:HGNC:35351]"}, {"versioned_ensembl_gene_id":"ENSG00000278109.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":43607436,"end":43607723,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276296.1","gene_symbol":"TFPT","gene_name":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]","synonyms":"FB1,FB1,INO80F,INO80F,amida,amida","biotype":"protein_coding","ncbi_id":"29844","summary":null,"start":54107066,"end":54115801,"strand":-1,"description":"TCF3 fusion partner [Source:HGNC Symbol;Acc:HGNC:13630]"}, {"versioned_ensembl_gene_id":"ENSG00000201969.1","gene_symbol":"SNORD115-20","gene_name":"small nucleolar RNA, C/D box 115-20 [Source:HGNC Symbol;Acc:HGNC:33039]","synonyms":"HBII-52-20","biotype":"snoRNA","ncbi_id":"100033460","summary":null,"start":25206262,"end":25206343,"strand":1,"description":"small nucleolar RNA, C/D box 115-20 [Source:HGNC Symbol;Acc:HGNC:33039]"}, {"versioned_ensembl_gene_id":"ENSG00000263442.1","gene_symbol":"SNORD84","gene_name":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]","synonyms":"U84,U84","biotype":"snoRNA","ncbi_id":"692199","summary":null,"start":31531850,"end":31531927,"strand":-1,"description":"small nucleolar RNA, C/D box 84 [Source:HGNC Symbol;Acc:HGNC:32743]"}, {"versioned_ensembl_gene_id":"ENSG00000221393.1","gene_symbol":"MIR1302-6","gene_name":"microRNA 1302-6 [Source:HGNC Symbol;Acc:HGNC:35298]","synonyms":"MIRN1302-6,hsa-mir-1302-6","biotype":"miRNA","ncbi_id":"100302140","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18127220,"end":18127309,"strand":-1,"description":"microRNA 1302-6 [Source:HGNC Symbol;Acc:HGNC:35298]"}, {"versioned_ensembl_gene_id":"ENSG00000252202.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":179847035,"end":179847130,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207637.1","gene_symbol":"MIR595","gene_name":"microRNA 595 [Source:HGNC Symbol;Acc:HGNC:32851]","synonyms":"MIRN595,hsa-mir-595","biotype":"miRNA","ncbi_id":"693180","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":158532718,"end":158532813,"strand":-1,"description":"microRNA 595 [Source:HGNC Symbol;Acc:HGNC:32851]"}, {"versioned_ensembl_gene_id":"ENSG00000200216.2","gene_symbol":"RNU6-745P","gene_name":"RNA, U6 small nuclear 745, pseudogene [Source:HGNC Symbol;Acc:HGNC:47708]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481415","summary":null,"start":70193236,"end":70193341,"strand":1,"description":"RNA, U6 small nuclear 745, pseudogene [Source:HGNC Symbol;Acc:HGNC:47708]"}, {"versioned_ensembl_gene_id":"ENSG00000207426.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":96701507,"end":96701619,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284351.1","gene_symbol":"MIR3622A","gene_name":"microRNA 3622a [Source:HGNC Symbol;Acc:HGNC:38934]","synonyms":"hsa-mir-3622a","biotype":"miRNA","ncbi_id":"100500858","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27701677,"end":27701759,"strand":1,"description":"microRNA 3622a [Source:HGNC Symbol;Acc:HGNC:38934]"}, {"versioned_ensembl_gene_id":"ENSG00000212295.1","gene_symbol":"SNORD28B","gene_name":"small nucleolar RNA, C/D box 28B [Source:HGNC Symbol;Acc:HGNC:52225]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617011","summary":null,"start":156378750,"end":156378824,"strand":1,"description":"small nucleolar RNA, C/D box 28B [Source:HGNC Symbol;Acc:HGNC:52225]"}, {"versioned_ensembl_gene_id":"ENSG00000243439.3","gene_symbol":"RN7SL352P","gene_name":"RNA, 7SL, cytoplasmic 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:46368]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479352","summary":null,"start":1507322,"end":1507598,"strand":1,"description":"RNA, 7SL, cytoplasmic 352, pseudogene [Source:HGNC Symbol;Acc:HGNC:46368]"}, {"versioned_ensembl_gene_id":"ENSG00000265847.1","gene_symbol":"MIR4287","gene_name":"microRNA 4287 [Source:HGNC Symbol;Acc:HGNC:38208]","synonyms":"hsa-mir-4287","biotype":"miRNA","ncbi_id":"100422828","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27886039,"end":27886116,"strand":-1,"description":"microRNA 4287 [Source:HGNC Symbol;Acc:HGNC:38208]"}, {"versioned_ensembl_gene_id":"ENSG00000206784.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37322259,"end":37322371,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265588.1","gene_symbol":"MIR5708","gene_name":"microRNA 5708 [Source:HGNC Symbol;Acc:HGNC:43511]","synonyms":"hsa-mir-5708","biotype":"miRNA","ncbi_id":"100847056","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":80241389,"end":80241473,"strand":1,"description":"microRNA 5708 [Source:HGNC Symbol;Acc:HGNC:43511]"}, {"versioned_ensembl_gene_id":"ENSG00000252674.1","gene_symbol":"RNA5SP102","gene_name":"RNA, 5S ribosomal pseudogene 102 [Source:HGNC Symbol;Acc:HGNC:42900]","synonyms":"RN5S102","biotype":"rRNA","ncbi_id":"100873373","summary":null,"start":124932915,"end":124933020,"strand":1,"description":"RNA, 5S ribosomal pseudogene 102 [Source:HGNC Symbol;Acc:HGNC:42900]"}, {"versioned_ensembl_gene_id":"ENSG00000238379.1","gene_symbol":"RNA5SP103","gene_name":"RNA, 5S ribosomal pseudogene 103 [Source:HGNC Symbol;Acc:HGNC:42901]","synonyms":"RN5S103","biotype":"rRNA","ncbi_id":"100873374","summary":null,"start":128445081,"end":128445198,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 103 [Source:HGNC Symbol;Acc:HGNC:42901]"}, {"versioned_ensembl_gene_id":"ENSG00000201648.1","gene_symbol":"RNU4-91P","gene_name":"RNA, U4 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47027]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481201","summary":null,"start":175609479,"end":175609613,"strand":1,"description":"RNA, U4 small nuclear 91, pseudogene [Source:HGNC Symbol;Acc:HGNC:47027]"}, {"versioned_ensembl_gene_id":"ENSG00000252263.1","gene_symbol":"RNU6-659P","gene_name":"RNA, U6 small nuclear 659, pseudogene [Source:HGNC Symbol;Acc:HGNC:47622]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481390","summary":null,"start":70496107,"end":70496210,"strand":1,"description":"RNA, U6 small nuclear 659, pseudogene [Source:HGNC Symbol;Acc:HGNC:47622]"}, {"versioned_ensembl_gene_id":"ENSG00000212014.1","gene_symbol":"MIR509-3","gene_name":"microRNA 509-3 [Source:HGNC Symbol;Acc:HGNC:33675]","synonyms":"MIRN509-3,hsa-mir-509-3","biotype":"miRNA","ncbi_id":"100126337","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147259652,"end":147259726,"strand":-1,"description":"microRNA 509-3 [Source:HGNC Symbol;Acc:HGNC:33675]"}, {"versioned_ensembl_gene_id":"ENSG00000252823.1","gene_symbol":"RNU6-148P","gene_name":"RNA, U6 small nuclear 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:47111]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479631","summary":null,"start":89754059,"end":89754152,"strand":1,"description":"RNA, U6 small nuclear 148, pseudogene [Source:HGNC Symbol;Acc:HGNC:47111]"}, {"versioned_ensembl_gene_id":"ENSG00000207370.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":193624189,"end":193624301,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000251768.1","gene_symbol":"RNA5SP217","gene_name":"RNA, 5S ribosomal pseudogene 217 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000222536.1","gene_symbol":"RNU2-39P","gene_name":"RNA, U2 small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:48532]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480214","summary":null,"start":72721806,"end":72722003,"strand":1,"description":"RNA, U2 small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:48532]"}, {"versioned_ensembl_gene_id":"ENSG00000239112.1","gene_symbol":"SNORD123","gene_name":"small nucleolar RNA, C/D box 123 [Source:HGNC Symbol;Acc:HGNC:33562]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113384","summary":null,"start":9548836,"end":9548905,"strand":1,"description":"small nucleolar RNA, C/D box 123 [Source:HGNC Symbol;Acc:HGNC:33562]"}, {"versioned_ensembl_gene_id":"ENSG00000207313.1","gene_symbol":"SNORA2B","gene_name":"small nucleolar RNA, H/ACA box 2B [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000276826.1","gene_symbol":"RDH13","gene_name":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]","synonyms":"SDR7C3,SDR7C3","biotype":"protein_coding","ncbi_id":"112724","summary":"This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. 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[provided by RefSeq, Mar 2009]","start":54715159,"end":54734052,"strand":-1,"description":"retinol dehydrogenase 13 [Source:HGNC Symbol;Acc:HGNC:19978]"}, {"versioned_ensembl_gene_id":"ENSG00000199705.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":123857062,"end":123857163,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000272445.1","gene_symbol":"RNU6-84P","gene_name":"RNA, U6 small nuclear 84, pseudogene [Source:HGNC Symbol;Acc:HGNC:47047]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479603","summary":null,"start":76557653,"end":76557754,"strand":-1,"description":"RNA, U6 small nuclear 84, pseudogene [Source:HGNC Symbol;Acc:HGNC:47047]"}, {"versioned_ensembl_gene_id":"ENSG00000274342.1","gene_symbol":"TTC28-AS1_3","gene_name":"TTC28 antisense RNA 1 conserved region 3 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{"versioned_ensembl_gene_id":"ENSG00000201950.1","gene_symbol":"SNORD113-9","gene_name":"small nucleolar RNA, C/D box 113-9 [Source:HGNC Symbol;Acc:HGNC:32988]","synonyms":"14q(I-9)","biotype":"snoRNA","ncbi_id":"767569","summary":null,"start":100945649,"end":100945720,"strand":1,"description":"small nucleolar RNA, C/D box 113-9 [Source:HGNC Symbol;Acc:HGNC:32988]"}, {"versioned_ensembl_gene_id":"ENSG00000212457.1","gene_symbol":"RNU6-644P","gene_name":"RNA, U6 small nuclear 644, pseudogene [Source:HGNC Symbol;Acc:HGNC:47607]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481385","summary":null,"start":116188455,"end":116188552,"strand":-1,"description":"RNA, U6 small nuclear 644, pseudogene [Source:HGNC Symbol;Acc:HGNC:47607]"}, {"versioned_ensembl_gene_id":"ENSG00000252338.1","gene_symbol":"RNU6-503P","gene_name":"RNA, U6 small nuclear 503, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000241869.3","gene_symbol":"RN7SL363P","gene_name":"RNA, 7SL, cytoplasmic 363, pseudogene [Source:HGNC Symbol;Acc:HGNC:46379]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480504","summary":null,"start":90855935,"end":90856207,"strand":-1,"description":"RNA, 7SL, cytoplasmic 363, pseudogene [Source:HGNC Symbol;Acc:HGNC:46379]"}, {"versioned_ensembl_gene_id":"ENSG00000273916.4","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"LY94,CD335,NKP46,NK-p46,LY94,CD335,NKP46,NK-p46","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54850138,"end":54857077,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000252513.1","gene_symbol":"RNU1-128P","gene_name":"RNA, U1 small nuclear 128, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000266720.2","gene_symbol":"RN7SL14P","gene_name":"RNA, 7SL, cytoplasmic 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46030]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480481","summary":null,"start":18258554,"end":18258851,"strand":-1,"description":"RNA, 7SL, cytoplasmic 14, pseudogene [Source:HGNC Symbol;Acc:HGNC:46030]"}, {"versioned_ensembl_gene_id":"ENSG00000241745.3","gene_symbol":"RN7SL788P","gene_name":"RNA, 7SL, cytoplasmic 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:46804]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481135","summary":null,"start":52150104,"end":52150419,"strand":1,"description":"RNA, 7SL, cytoplasmic 788, pseudogene [Source:HGNC Symbol;Acc:HGNC:46804]"}, {"versioned_ensembl_gene_id":"ENSG00000273905.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":15298518,"end":15298617,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000238489.1","gene_symbol":"RNU6-749P","gene_name":"RNA, U6 small nuclear 749, pseudogene [Source:HGNC Symbol;Acc:HGNC:47712]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480606","summary":null,"start":20855251,"end":20855357,"strand":-1,"description":"RNA, U6 small nuclear 749, pseudogene [Source:HGNC Symbol;Acc:HGNC:47712]"}, {"versioned_ensembl_gene_id":"ENSG00000212181.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":148260574,"end":148260708,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000212511.2","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":36852640,"end":36852859,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000201343.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":177120691,"end":177120800,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278072.1","gene_symbol":"TUSC7","gene_name":"Non-coding RNA LOC285194 [Source:RFAM;Acc:RF01879]","synonyms":"NCRNA00295,LSAMP-AS3,LOC285194,LINC00902","biotype":"misc_RNA","ncbi_id":"285194","summary":null,"start":116716460,"end":116716624,"strand":1,"description":"Non-coding RNA LOC285194 [Source:RFAM;Acc:RF01879]"}, {"versioned_ensembl_gene_id":"ENSG00000274965.4","gene_symbol":"TRPM1","gene_name":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]","synonyms":"LTRPC1,CSNB1C,MLSN1,LTRPC1,CSNB1C,MLSN1","biotype":"protein_coding","ncbi_id":"4308","summary":"This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]","start":31152534,"end":31312750,"strand":-1,"description":"transient receptor potential cation channel subfamily M member 1 [Source:HGNC Symbol;Acc:HGNC:7146]"}, {"versioned_ensembl_gene_id":"ENSG00000276766.1","gene_symbol":"AC012314.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54102906,"end":54107026,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000241333.3","gene_symbol":"RN7SL385P","gene_name":"RNA, 7SL, cytoplasmic 385, pseudogene [Source:HGNC Symbol;Acc:HGNC:46401]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481840","summary":null,"start":37669464,"end":37669739,"strand":-1,"description":"RNA, 7SL, cytoplasmic 385, pseudogene [Source:HGNC Symbol;Acc:HGNC:46401]"}, {"versioned_ensembl_gene_id":"ENSG00000283899.1","gene_symbol":"MIR761","gene_name":"microRNA 761 [Source:HGNC Symbol;Acc:HGNC:37305]","synonyms":"hsa-mir-761","biotype":"miRNA","ncbi_id":"100313892","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":51836344,"end":51836402,"strand":-1,"description":"microRNA 761 [Source:HGNC Symbol;Acc:HGNC:37305]"}, {"versioned_ensembl_gene_id":"ENSG00000265061.1","gene_symbol":"MIR4419B","gene_name":"microRNA 4419b [Source:HGNC Symbol;Acc:HGNC:41724]","synonyms":"hsa-mir-4419b","biotype":"miRNA","ncbi_id":"100616298","summary":"This record was withdrawn by miRBase.","start":128244506,"end":128244573,"strand":1,"description":"microRNA 4419b [Source:HGNC Symbol;Acc:HGNC:41724]"}, {"versioned_ensembl_gene_id":"ENSG00000252756.1","gene_symbol":"RNU6-577P","gene_name":"RNA, U6 small nuclear 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:47540]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479822","summary":null,"start":36867398,"end":36867495,"strand":-1,"description":"RNA, U6 small nuclear 577, pseudogene [Source:HGNC Symbol;Acc:HGNC:47540]"}, {"versioned_ensembl_gene_id":"ENSG00000221537.1","gene_symbol":"MIR548H1","gene_name":"microRNA 548h-1 [Source:HGNC Symbol;Acc:HGNC:35342]","synonyms":"MIRN548H1,hsa-mir-548h-1","biotype":"miRNA","ncbi_id":"100313830","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64095024,"end":64095125,"strand":-1,"description":"microRNA 548h-1 [Source:HGNC Symbol;Acc:HGNC:35342]"}, {"versioned_ensembl_gene_id":"ENSG00000199843.1","gene_symbol":"RNA5SP358","gene_name":"RNA, 5S ribosomal pseudogene 358 [Source:HGNC Symbol;Acc:HGNC:43258]","synonyms":"RN5S358","biotype":"rRNA","ncbi_id":"100873617","summary":null,"start":38161466,"end":38161582,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 358 [Source:HGNC Symbol;Acc:HGNC:43258]"}, {"versioned_ensembl_gene_id":"ENSG00000199109.4","gene_symbol":"MIR411","gene_name":"microRNA 411 [Source:HGNC Symbol;Acc:HGNC:32792]","synonyms":"MIRN411,hsa-mir-411","biotype":"miRNA","ncbi_id":"693121","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101023325,"end":101023420,"strand":1,"description":"microRNA 411 [Source:HGNC Symbol;Acc:HGNC:32792]"}, {"versioned_ensembl_gene_id":"ENSG00000211582.1","gene_symbol":"MIR758","gene_name":"microRNA 758 [Source:HGNC Symbol;Acc:HGNC:33133]","synonyms":"MIRN758,hsa-mir-758","biotype":"miRNA","ncbi_id":"768212","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101026020,"end":101026107,"strand":1,"description":"microRNA 758 [Source:HGNC Symbol;Acc:HGNC:33133]"}, {"versioned_ensembl_gene_id":"ENSG00000272359.1","gene_symbol":"RNU4-89P","gene_name":"RNA, U4 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:47025]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481200","summary":null,"start":196747192,"end":196747324,"strand":-1,"description":"RNA, U4 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:47025]"}, {"versioned_ensembl_gene_id":"ENSG00000222236.1","gene_symbol":"RNA5SP163","gene_name":"RNA, 5S ribosomal pseudogene 163 [Source:HGNC Symbol;Acc:HGNC:43063]","synonyms":"RN5S163","biotype":"rRNA","ncbi_id":"100873428","summary":null,"start":71759518,"end":71759616,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 163 [Source:HGNC Symbol;Acc:HGNC:43063]"}, {"versioned_ensembl_gene_id":"ENSG00000263833.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31478704,"end":31478805,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222386.1","gene_symbol":"RN7SKP86","gene_name":"RNA, 7SK small nuclear pseudogene 86 [Source:HGNC Symbol;Acc:HGNC:45810]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480859","summary":null,"start":103484208,"end":103484539,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 86 [Source:HGNC Symbol;Acc:HGNC:45810]"}, {"versioned_ensembl_gene_id":"ENSG00000212584.1","gene_symbol":"RNU6-587P","gene_name":"RNA, U6 small nuclear 587, pseudogene [Source:HGNC Symbol;Acc:HGNC:47550]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481366","summary":null,"start":101691580,"end":101691685,"strand":1,"description":"RNA, U6 small nuclear 587, pseudogene [Source:HGNC Symbol;Acc:HGNC:47550]"}, {"versioned_ensembl_gene_id":"ENSG00000283180.1","gene_symbol":"MIR6767","gene_name":"microRNA 6767 [Source:HGNC Symbol;Acc:HGNC:50133]","synonyms":"hsa-mir-6767","biotype":"miRNA","ncbi_id":"102465459","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2445392,"end":2445457,"strand":1,"description":"microRNA 6767 [Source:HGNC Symbol;Acc:HGNC:50133]"}, {"versioned_ensembl_gene_id":"ENSG00000277403.1","gene_symbol":"CR547123.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":29063961,"end":29076488,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284564.1","gene_symbol":"MIR3064","gene_name":"microRNA 3064 [Source:HGNC Symbol;Acc:HGNC:41652]","synonyms":"hsa-mir-3064","biotype":"miRNA","ncbi_id":"100616387","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64500774,"end":64500839,"strand":-1,"description":"microRNA 3064 [Source:HGNC Symbol;Acc:HGNC:41652]"}, {"versioned_ensembl_gene_id":"ENSG00000266437.1","gene_symbol":"MIR4746","gene_name":"microRNA 4746 [Source:HGNC Symbol;Acc:HGNC:41904]","synonyms":"hsa-mir-4746","biotype":"miRNA","ncbi_id":"100616371","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":4445978,"end":4446048,"strand":1,"description":"microRNA 4746 [Source:HGNC Symbol;Acc:HGNC:41904]"}, {"versioned_ensembl_gene_id":"ENSG00000223191.1","gene_symbol":"RNU6-293P","gene_name":"RNA, U6 small nuclear 293, pseudogene [Source:HGNC Symbol;Acc:HGNC:47256]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481271","summary":null,"start":158926466,"end":158926571,"strand":-1,"description":"RNA, U6 small nuclear 293, pseudogene [Source:HGNC Symbol;Acc:HGNC:47256]"}, {"versioned_ensembl_gene_id":"ENSG00000221445.3","gene_symbol":"MIR1301","gene_name":"microRNA 1301 [Source:HGNC Symbol;Acc:HGNC:35253]","synonyms":"MIRN1301,hsa-mir-1301","biotype":"miRNA","ncbi_id":"100302246","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25328640,"end":25328721,"strand":-1,"description":"microRNA 1301 [Source:HGNC Symbol;Acc:HGNC:35253]"}, {"versioned_ensembl_gene_id":"ENSG00000265057.1","gene_symbol":"MIR4765","gene_name":"microRNA 4765 [Source:HGNC Symbol;Acc:HGNC:41791]","synonyms":"hsa-mir-4765","biotype":"miRNA","ncbi_id":"100616219","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":32635255,"end":32635331,"strand":1,"description":"microRNA 4765 [Source:HGNC Symbol;Acc:HGNC:41791]"}, {"versioned_ensembl_gene_id":"ENSG00000223080.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8943380,"end":8943467,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000276604.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000264755.1","gene_symbol":"MIR3131","gene_name":"microRNA 3131 [Source:HGNC Symbol;Acc:HGNC:38347]","synonyms":"hsa-mir-3131","biotype":"miRNA","ncbi_id":"100422957","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":219058688,"end":219058750,"strand":-1,"description":"microRNA 3131 [Source:HGNC Symbol;Acc:HGNC:38347]"}, {"versioned_ensembl_gene_id":"ENSG00000273745.1","gene_symbol":"MIR6870","gene_name":"microRNA 6870 [Source:HGNC Symbol;Acc:HGNC:50184]","synonyms":"hsa-mir-6870","biotype":"miRNA","ncbi_id":"102465525","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":10649636,"end":10649695,"strand":-1,"description":"microRNA 6870 [Source:HGNC Symbol;Acc:HGNC:50184]"}, {"versioned_ensembl_gene_id":"ENSG00000277437.1","gene_symbol":"MIR3687-1","gene_name":"microRNA 3687-1 [Source:HGNC Symbol;Acc:HGNC:38946]","synonyms":"MIR3687,hsa-mir-3687","biotype":"miRNA","ncbi_id":"100500815","summary":"This record was withdrawn by miRBase.","start":8208844,"end":8208904,"strand":1,"description":"microRNA 3687-1 [Source:HGNC Symbol;Acc:HGNC:38946]"}, {"versioned_ensembl_gene_id":"ENSG00000207359.1","gene_symbol":"RNU6-925P","gene_name":"RNA, U6 small nuclear 925, pseudogene [Source:HGNC Symbol;Acc:HGNC:47888]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479975","summary":null,"start":89900721,"end":89900824,"strand":-1,"description":"RNA, U6 small nuclear 925, pseudogene [Source:HGNC Symbol;Acc:HGNC:47888]"}, {"versioned_ensembl_gene_id":"ENSG00000275469.1","gene_symbol":"MIR6130","gene_name":"microRNA 6130 [Source:HGNC Symbol;Acc:HGNC:50156]","synonyms":"hsa-mir-6130","biotype":"miRNA","ncbi_id":"102466967","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":23079284,"end":23079392,"strand":1,"description":"microRNA 6130 [Source:HGNC Symbol;Acc:HGNC:50156]"}, {"versioned_ensembl_gene_id":"ENSG00000266645.1","gene_symbol":"MIR4299","gene_name":"microRNA 4299 [Source:HGNC Symbol;Acc:HGNC:38329]","synonyms":"hsa-mir-4299","biotype":"miRNA","ncbi_id":"100423026","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":11656651,"end":11656722,"strand":-1,"description":"microRNA 4299 [Source:HGNC Symbol;Acc:HGNC:38329]"}, {"versioned_ensembl_gene_id":"ENSG00000199218.1","gene_symbol":"RN7SKP184","gene_name":"RNA, 7SK small nuclear pseudogene 184 [Source:HGNC Symbol;Acc:HGNC:45908]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480470","summary":null,"start":53097652,"end":53097984,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 184 [Source:HGNC Symbol;Acc:HGNC:45908]"}, {"versioned_ensembl_gene_id":"ENSG00000207807.1","gene_symbol":"MIR95","gene_name":"microRNA 95 [Source:HGNC Symbol;Acc:HGNC:31647]","synonyms":"MIRN95,hsa-mir-95","biotype":"miRNA","ncbi_id":"407052","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8005301,"end":8005381,"strand":-1,"description":"microRNA 95 [Source:HGNC Symbol;Acc:HGNC:31647]"}, {"versioned_ensembl_gene_id":"ENSG00000266703.1","gene_symbol":"MIR4490","gene_name":"microRNA 4490 [Source:HGNC Symbol;Acc:HGNC:41871]","synonyms":"hsa-mir-4490","biotype":"miRNA","ncbi_id":"100616186","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":90555774,"end":90555857,"strand":-1,"description":"microRNA 4490 [Source:HGNC Symbol;Acc:HGNC:41871]"}, {"versioned_ensembl_gene_id":"ENSG00000271899.1","gene_symbol":"MIR4466","gene_name":"microRNA 4466 [Source:HGNC Symbol;Acc:HGNC:41726]","synonyms":"hsa-mir-4466","biotype":"miRNA","ncbi_id":"100616154","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":156779678,"end":156779731,"strand":-1,"description":"microRNA 4466 [Source:HGNC Symbol;Acc:HGNC:41726]"}, {"versioned_ensembl_gene_id":"ENSG00000277966.1","gene_symbol":"HOXA11-AS1_4","gene_name":"HOXA11 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02140]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27186892,"end":27187124,"strand":1,"description":"HOXA11 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02140]"}, {"versioned_ensembl_gene_id":"ENSG00000263978.1","gene_symbol":"MIR4499","gene_name":"microRNA 4499 [Source:HGNC Symbol;Acc:HGNC:41739]","synonyms":"hsa-mir-4499","biotype":"miRNA","ncbi_id":"100616304","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20433778,"end":20433846,"strand":-1,"description":"microRNA 4499 [Source:HGNC Symbol;Acc:HGNC:41739]"}, {"versioned_ensembl_gene_id":"ENSG00000252425.1","gene_symbol":"SNORA18","gene_name":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]","synonyms":"ACA18","biotype":"snoRNA","ncbi_id":"677805","summary":null,"start":34597458,"end":34597558,"strand":-1,"description":"Small nucleolar RNA SNORA18 [Source:RFAM;Acc:RF00425]"}, {"versioned_ensembl_gene_id":"ENSG00000273836.1","gene_symbol":"MIR6842","gene_name":"microRNA 6842 [Source:HGNC Symbol;Acc:HGNC:50254]","synonyms":"hsa-mir-6842","biotype":"miRNA","ncbi_id":"102465507","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27433370,"end":27433434,"strand":1,"description":"microRNA 6842 [Source:HGNC Symbol;Acc:HGNC:50254]"}, {"versioned_ensembl_gene_id":"ENSG00000221525.1","gene_symbol":"MIR1185-1","gene_name":"microRNA 1185-1 [Source:HGNC Symbol;Acc:HGNC:35257]","synonyms":"MIRN1185-1,hsa-mir-1185-1","biotype":"miRNA","ncbi_id":"100302157","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101042977,"end":101043062,"strand":1,"description":"microRNA 1185-1 [Source:HGNC Symbol;Acc:HGNC:35257]"}, {"versioned_ensembl_gene_id":"ENSG00000265075.1","gene_symbol":"MIR3622B","gene_name":"microRNA 3622b [Source:HGNC Symbol;Acc:HGNC:38961]","synonyms":"hsa-mir-3622b","biotype":"miRNA","ncbi_id":"100500871","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27701673,"end":27701767,"strand":-1,"description":"microRNA 3622b [Source:HGNC Symbol;Acc:HGNC:38961]"}, {"versioned_ensembl_gene_id":"ENSG00000199940.1","gene_symbol":"RN7SKP75","gene_name":"RNA, 7SK small nuclear pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:45799]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480856","summary":null,"start":71685452,"end":71685747,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 75 [Source:HGNC Symbol;Acc:HGNC:45799]"}, {"versioned_ensembl_gene_id":"ENSG00000266454.1","gene_symbol":"MIR3179-3","gene_name":"microRNA 3179-3 [Source:HGNC Symbol;Acc:HGNC:38214]","synonyms":"hsa-mir-3179-3","biotype":"miRNA","ncbi_id":"100423006","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18411894,"end":18411977,"strand":-1,"description":"microRNA 3179-3 [Source:HGNC Symbol;Acc:HGNC:38214]"}, {"versioned_ensembl_gene_id":"ENSG00000283874.1","gene_symbol":"MIR3911","gene_name":"microRNA 3911 [Source:HGNC Symbol;Acc:HGNC:38962]","synonyms":"hsa-mir-3911","biotype":"miRNA","ncbi_id":"100500872","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127690687,"end":127690795,"strand":-1,"description":"microRNA 3911 [Source:HGNC Symbol;Acc:HGNC:38962]"}, {"versioned_ensembl_gene_id":"ENSG00000278320.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36285684,"end":36285785,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277774.1","gene_symbol":"RN7SL763P","gene_name":"RNA, 7SL, cytoplasmic 763, pseudogene [Source:HGNC Symbol;Acc:HGNC:46779]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481130","summary":null,"start":39886861,"end":39887144,"strand":-1,"description":"RNA, 7SL, cytoplasmic 763, pseudogene [Source:HGNC Symbol;Acc:HGNC:46779]"}, {"versioned_ensembl_gene_id":"ENSG00000207838.1","gene_symbol":"MIR517C","gene_name":"microRNA 517c [Source:HGNC Symbol;Acc:HGNC:32124]","synonyms":"MIRN517C,hsa-mir-517c","biotype":"miRNA","ncbi_id":"574492","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53741313,"end":53741407,"strand":1,"description":"microRNA 517c [Source:HGNC Symbol;Acc:HGNC:32124]"}, {"versioned_ensembl_gene_id":"ENSG00000275661.1","gene_symbol":"H19_3","gene_name":"H19 conserved region 3 [Source:RFAM;Acc:RF01974]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52895,"end":53010,"strand":1,"description":"H19 conserved region 3 [Source:RFAM;Acc:RF01974]"}, {"versioned_ensembl_gene_id":"ENSG00000275558.1","gene_symbol":"RN7SKP175","gene_name":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479173","summary":null,"start":143542110,"end":143542398,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:45899]"}, {"versioned_ensembl_gene_id":"ENSG00000283333.1","gene_symbol":"MIR7977","gene_name":"microRNA 7977 [Source:HGNC Symbol;Acc:HGNC:49969]","synonyms":"hsa-mir-7977","biotype":"miRNA","ncbi_id":"102465858","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":176515103,"end":176515151,"strand":1,"description":"microRNA 7977 [Source:HGNC Symbol;Acc:HGNC:49969]"}, {"versioned_ensembl_gene_id":"ENSG00000243049.3","gene_symbol":"RN7SL33P","gene_name":"RNA, 7SL, cytoplasmic 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:46049]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479236","summary":null,"start":2557753,"end":2558094,"strand":-1,"description":"RNA, 7SL, cytoplasmic 33, pseudogene [Source:HGNC Symbol;Acc:HGNC:46049]"}, {"versioned_ensembl_gene_id":"ENSG00000222395.2","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":32263135,"end":32263234,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283468.1","gene_symbol":"MIR4454","gene_name":"microRNA 4454 [Source:HGNC Symbol;Acc:HGNC:41553]","synonyms":"hsa-mir-4454","biotype":"miRNA","ncbi_id":"100616234","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":163093574,"end":163093628,"strand":-1,"description":"microRNA 4454 [Source:HGNC Symbol;Acc:HGNC:41553]"}, {"versioned_ensembl_gene_id":"ENSG00000251733.1","gene_symbol":"SCARNA8","gene_name":"small Cajal body-specific RNA 8 [Source:HGNC Symbol;Acc:HGNC:32564]","synonyms":"U92","biotype":"scaRNA","ncbi_id":"677776","summary":null,"start":19063656,"end":19063786,"strand":-1,"description":"small Cajal body-specific RNA 8 [Source:HGNC Symbol;Acc:HGNC:32564]"}, {"versioned_ensembl_gene_id":"ENSG00000202601.4","gene_symbol":"MIR582","gene_name":"microRNA 582 [Source:HGNC Symbol;Acc:HGNC:32838]","synonyms":"MIRN582,hsa-mir-582","biotype":"miRNA","ncbi_id":"693167","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59703606,"end":59703703,"strand":-1,"description":"microRNA 582 [Source:HGNC Symbol;Acc:HGNC:32838]"}, {"versioned_ensembl_gene_id":"ENSG00000251907.1","gene_symbol":"RNU6-240P","gene_name":"RNA, U6 small nuclear 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:47203]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479673","summary":null,"start":73659564,"end":73659660,"strand":-1,"description":"RNA, U6 small nuclear 240, pseudogene [Source:HGNC Symbol;Acc:HGNC:47203]"}, {"versioned_ensembl_gene_id":"ENSG00000283493.1","gene_symbol":"MIR6086","gene_name":"microRNA 6086 [Source:HGNC Symbol;Acc:HGNC:49986]","synonyms":"hsa-mir-6086","biotype":"miRNA","ncbi_id":"102466519","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. 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Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT2 and GSTT2B are nearly identical to each other, and share 55% amino acid identity with GSTT1. All three genes may play a role in human carcinogenesis. The GSTT2B gene is a pseudogene in some populations. [provided by RefSeq, Sep 2015]","start":23957418,"end":23961206,"strand":-1,"description":"glutathione S-transferase theta 2B (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:33437]"}, {"versioned_ensembl_gene_id":"ENSG00000222990.1","gene_symbol":"RNU4-22P","gene_name":"RNA, U4 small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46958]","synonyms":null,"biotype":"snRNA","ncbi_id":"107057646","summary":null,"start":88513498,"end":88513663,"strand":1,"description":"RNA, U4 small nuclear 22, pseudogene [Source:HGNC Symbol;Acc:HGNC:46958]"}, {"versioned_ensembl_gene_id":"ENSG00000252826.1","gene_symbol":"RNU1-92P","gene_name":"RNA, U1 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:48434]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481620","summary":null,"start":143720510,"end":143720644,"strand":-1,"description":"RNA, U1 small nuclear 92, pseudogene [Source:HGNC Symbol;Acc:HGNC:48434]"}, 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{"versioned_ensembl_gene_id":"ENSG00000276675.1","gene_symbol":"TTC28-AS1_4","gene_name":"TTC28 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02201]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28002484,"end":28002595,"strand":1,"description":"TTC28 antisense RNA 1 conserved region 4 [Source:RFAM;Acc:RF02201]"}, {"versioned_ensembl_gene_id":"ENSG00000275070.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":129796491,"end":129796783,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000239825.3","gene_symbol":"RN7SL549P","gene_name":"RNA, 7SL, cytoplasmic 549, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000199415.1","gene_symbol":"RNA5SP370","gene_name":"RNA, 5S ribosomal pseudogene 370 [Source:HGNC Symbol;Acc:HGNC:43270]","synonyms":"RN5S370","biotype":"rRNA","ncbi_id":"106480765","summary":null,"start":104125236,"end":104125356,"strand":1,"description":"RNA, 5S ribosomal pseudogene 370 [Source:HGNC Symbol;Acc:HGNC:43270]"}, {"versioned_ensembl_gene_id":"ENSG00000252832.1","gene_symbol":"RNU6-1212P","gene_name":"RNA, U6 small nuclear 1212, pseudogene [Source:HGNC Symbol;Acc:HGNC:48175]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481943","summary":null,"start":19792998,"end":19793101,"strand":-1,"description":"RNA, U6 small nuclear 1212, pseudogene [Source:HGNC Symbol;Acc:HGNC:48175]"}, {"versioned_ensembl_gene_id":"ENSG00000202182.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63848261,"end":63848362,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201884.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":121846600,"end":121846700,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281899.1","gene_symbol":"AL359736.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":24321126,"end":24321428,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000242912.3","gene_symbol":"RN7SL384P","gene_name":"RNA, 7SL, cytoplasmic 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:46400]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481028","summary":null,"start":114423770,"end":114424067,"strand":-1,"description":"RNA, 7SL, cytoplasmic 384, pseudogene [Source:HGNC Symbol;Acc:HGNC:46400]"}, {"versioned_ensembl_gene_id":"ENSG00000239504.3","gene_symbol":"RN7SL583P","gene_name":"RNA, 7SL, cytoplasmic 583, pseudogene [Source:HGNC Symbol;Acc:HGNC:46599]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481082","summary":null,"start":88477828,"end":88478114,"strand":-1,"description":"RNA, 7SL, cytoplasmic 583, pseudogene [Source:HGNC Symbol;Acc:HGNC:46599]"}, {"versioned_ensembl_gene_id":"ENSG00000263526.1","gene_symbol":"MIR378G","gene_name":"microRNA 378g [Source:HGNC Symbol;Acc:HGNC:41785]","synonyms":"hsa-mir-378g","biotype":"miRNA","ncbi_id":"100616321","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94745860,"end":94745900,"strand":-1,"description":"microRNA 378g [Source:HGNC Symbol;Acc:HGNC:41785]"}, {"versioned_ensembl_gene_id":"ENSG00000222744.1","gene_symbol":"RN7SKP166","gene_name":"RNA, 7SK small nuclear pseudogene 166 [Source:HGNC Symbol;Acc:HGNC:45890]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481814","summary":null,"start":66292683,"end":66292987,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 166 [Source:HGNC Symbol;Acc:HGNC:45890]"}, {"versioned_ensembl_gene_id":"ENSG00000243338.3","gene_symbol":"RN7SL307P","gene_name":"RNA, 7SL, cytoplasmic 307, pseudogene [Source:HGNC Symbol;Acc:HGNC:46323]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480500","summary":null,"start":49198900,"end":49199194,"strand":-1,"description":"RNA, 7SL, cytoplasmic 307, pseudogene [Source:HGNC Symbol;Acc:HGNC:46323]"}, {"versioned_ensembl_gene_id":"ENSG00000284489.1","gene_symbol":"MIR6751","gene_name":"microRNA 6751 [Source:HGNC Symbol;Acc:HGNC:49983]","synonyms":"hsa-mir-6751","biotype":"miRNA","ncbi_id":"102465449","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65129916,"end":65129978,"strand":-1,"description":"microRNA 6751 [Source:HGNC Symbol;Acc:HGNC:49983]"}, {"versioned_ensembl_gene_id":"ENSG00000221476.2","gene_symbol":"MIR1827","gene_name":"microRNA 1827 [Source:HGNC Symbol;Acc:HGNC:35391]","synonyms":"MIRN1827,hsa-mir-1827","biotype":"miRNA","ncbi_id":"100302217","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100189884,"end":100189949,"strand":1,"description":"microRNA 1827 [Source:HGNC Symbol;Acc:HGNC:35391]"}, {"versioned_ensembl_gene_id":"ENSG00000276908.1","gene_symbol":"MIR7106","gene_name":"microRNA 7106 [Source:HGNC Symbol;Acc:HGNC:50085]","synonyms":"hsa-mir-7106","biotype":"miRNA","ncbi_id":"102466222","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":113159113,"end":113159177,"strand":-1,"description":"microRNA 7106 [Source:HGNC Symbol;Acc:HGNC:50085]"}, {"versioned_ensembl_gene_id":"ENSG00000200456.1","gene_symbol":"RNU6-1097P","gene_name":"RNA, U6 small nuclear 1097, pseudogene [Source:HGNC Symbol;Acc:HGNC:48060]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480048","summary":null,"start":44503773,"end":44503879,"strand":-1,"description":"RNA, U6 small nuclear 1097, pseudogene [Source:HGNC Symbol;Acc:HGNC:48060]"}, {"versioned_ensembl_gene_id":"ENSG00000207118.1","gene_symbol":"SNORD14D","gene_name":"small nucleolar RNA, C/D box 14D [Source:HGNC Symbol;Acc:HGNC:30353]","synonyms":null,"biotype":"snoRNA","ncbi_id":"85390","summary":null,"start":123058909,"end":123058995,"strand":-1,"description":"small nucleolar RNA, C/D box 14D [Source:HGNC Symbol;Acc:HGNC:30353]"}, {"versioned_ensembl_gene_id":"ENSG00000264429.1","gene_symbol":"MIR3183","gene_name":"microRNA 3183 [Source:HGNC Symbol;Acc:HGNC:38237]","synonyms":"hsa-mir-3183","biotype":"miRNA","ncbi_id":"100422835","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1022476,"end":1022559,"strand":-1,"description":"microRNA 3183 [Source:HGNC Symbol;Acc:HGNC:38237]"}, {"versioned_ensembl_gene_id":"ENSG00000241162.3","gene_symbol":"RN7SL617P","gene_name":"RNA, 7SL, cytoplasmic 617, pseudogene [Source:HGNC Symbol;Acc:HGNC:46633]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481852","summary":null,"start":110439996,"end":110440303,"strand":-1,"description":"RNA, 7SL, cytoplasmic 617, pseudogene [Source:HGNC Symbol;Acc:HGNC:46633]"}, {"versioned_ensembl_gene_id":"ENSG00000283935.1","gene_symbol":"MIR423","gene_name":"microRNA 423 [Source:HGNC Symbol;Acc:HGNC:31880]","synonyms":"MIRN423,hsa-mir-423","biotype":"miRNA","ncbi_id":"494335","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":30117079,"end":30117172,"strand":1,"description":"microRNA 423 [Source:HGNC Symbol;Acc:HGNC:31880]"}, {"versioned_ensembl_gene_id":"ENSG00000199394.1","gene_symbol":"RNU6-600P","gene_name":"RNA, U6 small nuclear 600, pseudogene [Source:HGNC Symbol;Acc:HGNC:47563]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479831","summary":null,"start":48892130,"end":48892228,"strand":-1,"description":"RNA, U6 small nuclear 600, pseudogene [Source:HGNC Symbol;Acc:HGNC:47563]"}, {"versioned_ensembl_gene_id":"ENSG00000252023.1","gene_symbol":"RNU6-581P","gene_name":"RNA, U6 small nuclear 581, pseudogene [Source:HGNC Symbol;Acc:HGNC:47544]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479823","summary":null,"start":120672871,"end":120672975,"strand":1,"description":"RNA, U6 small nuclear 581, pseudogene [Source:HGNC Symbol;Acc:HGNC:47544]"}, {"versioned_ensembl_gene_id":"ENSG00000263690.2","gene_symbol":"hsa-mir-548d-2","gene_name":"hsa-mir-548d-2 [Source:miRBase;Acc:MI0003671]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":67471489,"end":67471585,"strand":-1,"description":"hsa-mir-548d-2 [Source:miRBase;Acc:MI0003671]"}, {"versioned_ensembl_gene_id":"ENSG00000278249.1","gene_symbol":"SCARNA2","gene_name":"small Cajal body-specific RNA 2 [Source:HGNC Symbol;Acc:HGNC:32558]","synonyms":"mgU2-25/61,HBII-382","biotype":"scaRNA","ncbi_id":"677766","summary":null,"start":109100193,"end":109100612,"strand":1,"description":"small Cajal body-specific RNA 2 [Source:HGNC Symbol;Acc:HGNC:32558]"}, {"versioned_ensembl_gene_id":"ENSG00000266392.1","gene_symbol":"MIR4740","gene_name":"microRNA 4740 [Source:HGNC Symbol;Acc:HGNC:41711]","synonyms":"hsa-mir-4740","biotype":"miRNA","ncbi_id":"100616294","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81400716,"end":81400778,"strand":-1,"description":"microRNA 4740 [Source:HGNC Symbol;Acc:HGNC:41711]"}, {"versioned_ensembl_gene_id":"ENSG00000275693.1","gene_symbol":"FAS-AS1","gene_name":"FAS antisense RNA 1 conserved region [Source:RFAM;Acc:RF02116]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100302740","summary":null,"start":88992370,"end":88992539,"strand":1,"description":"FAS antisense RNA 1 conserved region [Source:RFAM;Acc:RF02116]"}, {"versioned_ensembl_gene_id":"ENSG00000207490.1","gene_symbol":"RNU6-987P","gene_name":"RNA, U6 small nuclear 987, pseudogene [Source:HGNC Symbol;Acc:HGNC:47950]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480002","summary":null,"start":25383599,"end":25383702,"strand":1,"description":"RNA, U6 small nuclear 987, pseudogene [Source:HGNC Symbol;Acc:HGNC:47950]"}, {"versioned_ensembl_gene_id":"ENSG00000264297.2","gene_symbol":"MIR4433B","gene_name":"microRNA 4433b [Source:HGNC Symbol;Acc:HGNC:50258]","synonyms":"hsa-mir-4433b","biotype":"miRNA","ncbi_id":"102465833","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64340747,"end":64340848,"strand":-1,"description":"microRNA 4433b [Source:HGNC Symbol;Acc:HGNC:50258]"}, {"versioned_ensembl_gene_id":"ENSG00000201148.1","gene_symbol":"RNA5SP42","gene_name":"RNA, 5S ribosomal pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:42818]","synonyms":"RN5S42","biotype":"rRNA","ncbi_id":"100873281","summary":null,"start":34112949,"end":34113063,"strand":1,"description":"RNA, 5S ribosomal pseudogene 42 [Source:HGNC Symbol;Acc:HGNC:42818]"}, {"versioned_ensembl_gene_id":"ENSG00000253019.1","gene_symbol":"RN7SKP35","gene_name":"RNA, 7SK small nuclear pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:45759]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479111","summary":null,"start":151576766,"end":151576916,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 35 [Source:HGNC Symbol;Acc:HGNC:45759]"}, {"versioned_ensembl_gene_id":"ENSG00000264725.1","gene_symbol":"MIR3129","gene_name":"microRNA 3129 [Source:HGNC Symbol;Acc:HGNC:38217]","synonyms":"hsa-mir-3129","biotype":"miRNA","ncbi_id":"100422908","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":189133036,"end":189133111,"strand":-1,"description":"microRNA 3129 [Source:HGNC Symbol;Acc:HGNC:38217]"}, {"versioned_ensembl_gene_id":"ENSG00000273885.1","gene_symbol":"snoU2-30","gene_name":"Small nucleolar RNA U2-30 [Source:RFAM;Acc:RF00493]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":93721797,"end":93721866,"strand":1,"description":"Small nucleolar RNA U2-30 [Source:RFAM;Acc:RF00493]"}, {"versioned_ensembl_gene_id":"ENSG00000264616.1","gene_symbol":"MIR4755","gene_name":"microRNA 4755 [Source:HGNC Symbol;Acc:HGNC:41815]","synonyms":"hsa-mir-4755","biotype":"miRNA","ncbi_id":"100616434","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34049119,"end":34049190,"strand":1,"description":"microRNA 4755 [Source:HGNC Symbol;Acc:HGNC:41815]"}, {"versioned_ensembl_gene_id":"ENSG00000258045.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":55731264,"end":55731531,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000265675.2","gene_symbol":"RN7SL708P","gene_name":"RNA, 7SL, cytoplasmic 708, pseudogene [Source:HGNC Symbol;Acc:HGNC:46724]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479481","summary":null,"start":49081332,"end":49081630,"strand":1,"description":"RNA, 7SL, cytoplasmic 708, pseudogene [Source:HGNC Symbol;Acc:HGNC:46724]"}, {"versioned_ensembl_gene_id":"ENSG00000266140.1","gene_symbol":"MIR4533","gene_name":"microRNA 4533 [Source:HGNC Symbol;Acc:HGNC:41886]","synonyms":"hsa-mir-4533","biotype":"miRNA","ncbi_id":"100616362","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60478111,"end":60478181,"strand":1,"description":"microRNA 4533 [Source:HGNC Symbol;Acc:HGNC:41886]"}, {"versioned_ensembl_gene_id":"ENSG00000273961.1","gene_symbol":"HOXA11-AS1_1","gene_name":"HOXA11 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02137]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27185433,"end":27185530,"strand":1,"description":"HOXA11 antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02137]"}, {"versioned_ensembl_gene_id":"ENSG00000275692.1","gene_symbol":"MIR6724-4","gene_name":"microRNA 6724-4 [Source:HGNC Symbol;Acc:HGNC:50830]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504733","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":8432530,"end":8432621,"strand":1,"description":"microRNA 6724-4 [Source:HGNC Symbol;Acc:HGNC:50830]"}, {"versioned_ensembl_gene_id":"ENSG00000223096.1","gene_symbol":"RNU5E-9P","gene_name":"RNA, U5E small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42532]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873840","summary":null,"start":178142548,"end":178142651,"strand":1,"description":"RNA, U5E small nuclear 9, pseudogene [Source:HGNC Symbol;Acc:HGNC:42532]"}, {"versioned_ensembl_gene_id":"ENSG00000202529.1","gene_symbol":"SNORD18B","gene_name":"small nucleolar RNA, C/D box 18B [Source:HGNC Symbol;Acc:HGNC:32715]","synonyms":"U18B","biotype":"snoRNA","ncbi_id":"595099","summary":null,"start":66502020,"end":66502091,"strand":-1,"description":"small nucleolar RNA, C/D box 18B [Source:HGNC Symbol;Acc:HGNC:32715]"}, {"versioned_ensembl_gene_id":"ENSG00000239247.3","gene_symbol":"RN7SL589P","gene_name":"RNA, 7SL, cytoplasmic 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:46605]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479438","summary":null,"start":2316197,"end":2316506,"strand":-1,"description":"RNA, 7SL, cytoplasmic 589, pseudogene [Source:HGNC Symbol;Acc:HGNC:46605]"}, {"versioned_ensembl_gene_id":"ENSG00000266533.1","gene_symbol":"MIR3619","gene_name":"microRNA 3619 [Source:HGNC Symbol;Acc:HGNC:38998]","synonyms":"hsa-mir-3619","biotype":"miRNA","ncbi_id":"100500828","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":46091044,"end":46091126,"strand":1,"description":"microRNA 3619 [Source:HGNC Symbol;Acc:HGNC:38998]"}, {"versioned_ensembl_gene_id":"ENSG00000275991.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":1101777,"end":1102043,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200608.1","gene_symbol":"SNORD114-11","gene_name":"small nucleolar RNA, C/D box 114-11 [Source:HGNC Symbol;Acc:HGNC:32999]","synonyms":"14q(II-11)","biotype":"snoRNA","ncbi_id":"767589","summary":null,"start":100968111,"end":100968185,"strand":1,"description":"small nucleolar RNA, C/D box 114-11 [Source:HGNC Symbol;Acc:HGNC:32999]"}, {"versioned_ensembl_gene_id":"ENSG00000277388.1","gene_symbol":"MIR8053","gene_name":"microRNA 8053 [Source:HGNC Symbol;Acc:HGNC:50137]","synonyms":"hsa-mir-8053","biotype":"miRNA","ncbi_id":"102467004","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47652669,"end":47652743,"strand":1,"description":"microRNA 8053 [Source:HGNC Symbol;Acc:HGNC:50137]"}, {"versioned_ensembl_gene_id":"ENSG00000263728.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30740863,"end":30741114,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000212160.1","gene_symbol":"RNU6-205P","gene_name":"RNA, U6 small nuclear 205, pseudogene [Source:HGNC Symbol;Acc:HGNC:47168]","synonyms":null,"biotype":"snRNA","ncbi_id":"106633815","summary":null,"start":110278185,"end":110278291,"strand":1,"description":"RNA, U6 small nuclear 205, pseudogene [Source:HGNC Symbol;Acc:HGNC:47168]"}, {"versioned_ensembl_gene_id":"ENSG00000263712.1","gene_symbol":"MIR4639","gene_name":"microRNA 4639 [Source:HGNC Symbol;Acc:HGNC:41645]","synonyms":"hsa-mir-4639","biotype":"miRNA","ncbi_id":"100616269","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16141556,"end":16141624,"strand":1,"description":"microRNA 4639 [Source:HGNC Symbol;Acc:HGNC:41645]"}, {"versioned_ensembl_gene_id":"ENSG00000201164.1","gene_symbol":"RNU4-36P","gene_name":"RNA, U4 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46972]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479573","summary":null,"start":68535515,"end":68535658,"strand":1,"description":"RNA, U4 small nuclear 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:46972]"}, {"versioned_ensembl_gene_id":"ENSG00000276404.1","gene_symbol":"MIR6835","gene_name":"microRNA 6835 [Source:HGNC Symbol;Acc:HGNC:49963]","synonyms":"hsa-mir-6835","biotype":"miRNA","ncbi_id":"102465502","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":34240673,"end":34240736,"strand":1,"description":"microRNA 6835 [Source:HGNC Symbol;Acc:HGNC:49963]"}, {"versioned_ensembl_gene_id":"ENSG00000222774.1","gene_symbol":"RN7SKP121","gene_name":"RNA, 7SK small nuclear pseudogene 121 [Source:HGNC Symbol;Acc:HGNC:45845]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481811","summary":null,"start":127406028,"end":127406332,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 121 [Source:HGNC Symbol;Acc:HGNC:45845]"}, {"versioned_ensembl_gene_id":"ENSG00000238295.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":177345858,"end":177345961,"strand":-1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000238367.1","gene_symbol":"MIR2113","gene_name":"microRNA 2113 [Source:HGNC Symbol;Acc:HGNC:37058]","synonyms":"hsa-mir-2113","biotype":"miRNA","ncbi_id":"100302164","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":98024531,"end":98024621,"strand":1,"description":"microRNA 2113 [Source:HGNC Symbol;Acc:HGNC:37058]"}, {"versioned_ensembl_gene_id":"ENSG00000238300.1","gene_symbol":"SNORD121B","gene_name":"small nucleolar RNA, C/D box 121B [Source:HGNC Symbol;Acc:HGNC:33569]","synonyms":null,"biotype":"snoRNA","ncbi_id":"101340252","summary":null,"start":33934296,"end":33934376,"strand":-1,"description":"small nucleolar RNA, C/D box 121B [Source:HGNC Symbol;Acc:HGNC:33569]"}, {"versioned_ensembl_gene_id":"ENSG00000202216.2","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":179934402,"end":179934527,"strand":-1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000207692.3","gene_symbol":"MIR592","gene_name":"microRNA 592 [Source:HGNC Symbol;Acc:HGNC:32848]","synonyms":"MIRN592,hsa-mir-592","biotype":"miRNA","ncbi_id":"693177","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127058088,"end":127058184,"strand":-1,"description":"microRNA 592 [Source:HGNC Symbol;Acc:HGNC:32848]"}, {"versioned_ensembl_gene_id":"ENSG00000200378.1","gene_symbol":"RNU5B-4P","gene_name":"RNA, U5B small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:34184]","synonyms":null,"biotype":"snRNA","ncbi_id":"100147752","summary":null,"start":139447907,"end":139448017,"strand":1,"description":"RNA, U5B small nuclear 4, pseudogene [Source:HGNC Symbol;Acc:HGNC:34184]"}, {"versioned_ensembl_gene_id":"ENSG00000207990.3","gene_symbol":"MIR182","gene_name":"microRNA 182 [Source:HGNC Symbol;Acc:HGNC:31553]","synonyms":"MIRN182,hsa-mir-182","biotype":"miRNA","ncbi_id":"406958","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129770383,"end":129770492,"strand":-1,"description":"microRNA 182 [Source:HGNC Symbol;Acc:HGNC:31553]"}, {"versioned_ensembl_gene_id":"ENSG00000253028.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":52269437,"end":52269569,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000201850.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":68089449,"end":68089543,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207574.1","gene_symbol":"MIR661","gene_name":"microRNA 661 [Source:HGNC Symbol;Acc:HGNC:32917]","synonyms":"MIRN661,hsa-mir-661","biotype":"miRNA","ncbi_id":"724031","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":143945191,"end":143945279,"strand":-1,"description":"microRNA 661 [Source:HGNC Symbol;Acc:HGNC:32917]"}, {"versioned_ensembl_gene_id":"ENSG00000276351.1","gene_symbol":"H19_2","gene_name":"H19 conserved region 2 [Source:RFAM;Acc:RF01973]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":52666,"end":52734,"strand":1,"description":"H19 conserved region 2 [Source:RFAM;Acc:RF01973]"}, {"versioned_ensembl_gene_id":"ENSG00000264922.1","gene_symbol":"MIR4540","gene_name":"microRNA 4540 [Source:HGNC Symbol;Acc:HGNC:41670]","synonyms":"hsa-mir-4540","biotype":"miRNA","ncbi_id":"100616278","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36864254,"end":36864308,"strand":-1,"description":"microRNA 4540 [Source:HGNC Symbol;Acc:HGNC:41670]"}, {"versioned_ensembl_gene_id":"ENSG00000274932.1","gene_symbol":"MIR7150","gene_name":"microRNA 7150 [Source:HGNC Symbol;Acc:HGNC:49982]","synonyms":"hsa-mir-7150","biotype":"miRNA","ncbi_id":"102465688","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":123485529,"end":123485622,"strand":-1,"description":"microRNA 7150 [Source:HGNC Symbol;Acc:HGNC:49982]"}, {"versioned_ensembl_gene_id":"ENSG00000252015.1","gene_symbol":"RNU6-904P","gene_name":"RNA, U6 small nuclear 904, pseudogene [Source:HGNC Symbol;Acc:HGNC:47867]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479966","summary":null,"start":141167257,"end":141167357,"strand":-1,"description":"RNA, U6 small nuclear 904, pseudogene [Source:HGNC Symbol;Acc:HGNC:47867]"}, {"versioned_ensembl_gene_id":"ENSG00000223169.1","gene_symbol":"RNA5SP209","gene_name":"RNA, 5S ribosomal pseudogene 209 [Source:HGNC Symbol;Acc:HGNC:43109]","synonyms":"RN5S209","biotype":"rRNA","ncbi_id":"100873469","summary":null,"start":75865239,"end":75865335,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 209 [Source:HGNC Symbol;Acc:HGNC:43109]"}, {"versioned_ensembl_gene_id":"ENSG00000206701.1","gene_symbol":"RNU6-1040P","gene_name":"RNA, U6 small nuclear 1040, pseudogene [Source:HGNC Symbol;Acc:HGNC:48003]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480023","summary":null,"start":84665759,"end":84665865,"strand":-1,"description":"RNA, U6 small nuclear 1040, pseudogene [Source:HGNC Symbol;Acc:HGNC:48003]"}, {"versioned_ensembl_gene_id":"ENSG00000207484.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":51884556,"end":51884653,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207309.1","gene_symbol":"RNU4-70P","gene_name":"RNA, U4 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:47006]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480548","summary":null,"start":96649453,"end":96649591,"strand":-1,"description":"RNA, U4 small nuclear 70, pseudogene [Source:HGNC Symbol;Acc:HGNC:47006]"}, {"versioned_ensembl_gene_id":"ENSG00000274663.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":38144201,"end":38144287,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000199620.1","gene_symbol":"RNA5SP258","gene_name":"RNA, 5S ribosomal pseudogene 258 [Source:HGNC Symbol;Acc:HGNC:43158]","synonyms":"RN5S258","biotype":"rRNA","ncbi_id":"100873512","summary":null,"start":26136880,"end":26136998,"strand":1,"description":"RNA, 5S ribosomal pseudogene 258 [Source:HGNC Symbol;Acc:HGNC:43158]"}, {"versioned_ensembl_gene_id":"ENSG00000252782.1","gene_symbol":"RNU6-341P","gene_name":"RNA, U6 small nuclear 341, pseudogene [Source:HGNC Symbol;Acc:HGNC:47304]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481287","summary":null,"start":58292293,"end":58292388,"strand":-1,"description":"RNA, U6 small nuclear 341, pseudogene [Source:HGNC Symbol;Acc:HGNC:47304]"}, {"versioned_ensembl_gene_id":"ENSG00000199964.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":64834056,"end":64834157,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200741.1","gene_symbol":"RNA5SP161","gene_name":"RNA, 5S ribosomal pseudogene 161 [Source:HGNC Symbol;Acc:HGNC:43061]","synonyms":"RN5S161","biotype":"rRNA","ncbi_id":"106480757","summary":null,"start":56097390,"end":56097504,"strand":1,"description":"RNA, 5S ribosomal pseudogene 161 [Source:HGNC Symbol;Acc:HGNC:43061]"}, {"versioned_ensembl_gene_id":"ENSG00000206588.1","gene_symbol":"RNU1-28P","gene_name":"RNA, U1 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:37498]","synonyms":"RNU1-8P,RNU1-8","biotype":"snRNA","ncbi_id":"26866","summary":null,"start":34556226,"end":34556389,"strand":-1,"description":"RNA, U1 small nuclear 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:37498]"}, {"versioned_ensembl_gene_id":"ENSG00000207186.1","gene_symbol":"RNA5SP122","gene_name":"RNA, 5S ribosomal pseudogene 122 [Source:HGNC Symbol;Acc:HGNC:42920]","synonyms":"RN5S122","biotype":"rRNA","ncbi_id":"100873392","summary":null,"start":241584968,"end":241585075,"strand":1,"description":"RNA, 5S ribosomal pseudogene 122 [Source:HGNC Symbol;Acc:HGNC:42920]"}, {"versioned_ensembl_gene_id":"ENSG00000252691.1","gene_symbol":"SCARNA18","gene_name":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]","synonyms":"U109,SCARNA18A","biotype":"scaRNA","ncbi_id":"677765","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":26006216,"end":26006299,"strand":1,"description":"small Cajal body-specific RNA 18 [Source:RFAM;Acc:RF00283]"}, {"versioned_ensembl_gene_id":"ENSG00000222486.1","gene_symbol":"RNU6-77P","gene_name":"RNA, U6 small nuclear 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:42567]","synonyms":"RNU6-77","biotype":"snRNA","ncbi_id":"106481792","summary":null,"start":81265747,"end":81265837,"strand":1,"description":"RNA, U6 small nuclear 77, pseudogene [Source:HGNC Symbol;Acc:HGNC:42567]"}, {"versioned_ensembl_gene_id":"ENSG00000222522.1","gene_symbol":"RNU6-519P","gene_name":"RNA, U6 small nuclear 519, pseudogene [Source:HGNC Symbol;Acc:HGNC:47482]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479796","summary":null,"start":47979414,"end":47979521,"strand":1,"description":"RNA, U6 small nuclear 519, pseudogene [Source:HGNC Symbol;Acc:HGNC:47482]"}, {"versioned_ensembl_gene_id":"ENSG00000252049.1","gene_symbol":"SNORA40","gene_name":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]","synonyms":"SNORA40A,ACA40","biotype":"snoRNA","ncbi_id":"677822","summary":null,"start":23166985,"end":23167101,"strand":1,"description":"Small nucleolar RNA SNORA40 [Source:RFAM;Acc:RF00561]"}, {"versioned_ensembl_gene_id":"ENSG00000207210.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":173052452,"end":173052555,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252689.1","gene_symbol":"SNORA20","gene_name":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]","synonyms":"ACA20","biotype":"snoRNA","ncbi_id":"677806","summary":null,"start":16138248,"end":16138379,"strand":-1,"description":"Small nucleolar RNA SNORA20 [Source:RFAM;Acc:RF00401]"}, {"versioned_ensembl_gene_id":"ENSG00000274704.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":49913493,"end":49913760,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199279.1","gene_symbol":"RNU6-661P","gene_name":"RNA, U6 small nuclear 661, pseudogene [Source:HGNC Symbol;Acc:HGNC:47624]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479859","summary":null,"start":62443176,"end":62443282,"strand":1,"description":"RNA, U6 small nuclear 661, pseudogene [Source:HGNC Symbol;Acc:HGNC:47624]"}, {"versioned_ensembl_gene_id":"ENSG00000264887.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31855113,"end":31855201,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264994.1","gene_symbol":"SNORD92","gene_name":"small nucleolar RNA, C/D box 92 [Source:HGNC Symbol;Acc:HGNC:32754]","synonyms":"HBII-316","biotype":"snoRNA","ncbi_id":"692209","summary":null,"start":28913664,"end":28913748,"strand":1,"description":"small nucleolar RNA, C/D box 92 [Source:HGNC Symbol;Acc:HGNC:32754]"}, {"versioned_ensembl_gene_id":"ENSG00000241156.3","gene_symbol":"RN7SL582P","gene_name":"RNA, 7SL, cytoplasmic 582, pseudogene [Source:HGNC Symbol;Acc:HGNC:46598]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479435","summary":null,"start":116582552,"end":116582830,"strand":-1,"description":"RNA, 7SL, cytoplasmic 582, pseudogene [Source:HGNC Symbol;Acc:HGNC:46598]"}, {"versioned_ensembl_gene_id":"ENSG00000252498.1","gene_symbol":"RNU6-1016P","gene_name":"RNA, U6 small nuclear 1016, pseudogene [Source:HGNC Symbol;Acc:HGNC:47979]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480630","summary":null,"start":75644084,"end":75644177,"strand":1,"description":"RNA, U6 small nuclear 1016, pseudogene [Source:HGNC Symbol;Acc:HGNC:47979]"}, {"versioned_ensembl_gene_id":"ENSG00000206755.1","gene_symbol":"SNORA30","gene_name":"small nucleolar RNA, H/ACA box 30 [Source:HGNC Symbol;Acc:HGNC:32620]","synonyms":"SNORA30A,ACA30","biotype":"snoRNA","ncbi_id":"677813","summary":null,"start":30710537,"end":30710665,"strand":1,"description":"small nucleolar RNA, H/ACA box 30 [Source:HGNC Symbol;Acc:HGNC:32620]"}, {"versioned_ensembl_gene_id":"ENSG00000276729.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50019019,"end":50019320,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252008.1","gene_symbol":"RNU6-927P","gene_name":"RNA, U6 small nuclear 927, pseudogene [Source:HGNC Symbol;Acc:HGNC:47890]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479976","summary":null,"start":124901512,"end":124901611,"strand":1,"description":"RNA, U6 small nuclear 927, pseudogene [Source:HGNC Symbol;Acc:HGNC:47890]"}, {"versioned_ensembl_gene_id":"ENSG00000243051.3","gene_symbol":"RN7SL269P","gene_name":"RNA, 7SL, cytoplasmic 269, pseudogene [Source:HGNC Symbol;Acc:HGNC:46285]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479320","summary":null,"start":169957942,"end":169958246,"strand":-1,"description":"RNA, 7SL, cytoplasmic 269, pseudogene [Source:HGNC Symbol;Acc:HGNC:46285]"}, {"versioned_ensembl_gene_id":"ENSG00000275806.1","gene_symbol":"TARM1","gene_name":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441864","summary":null,"start":54069947,"end":54081380,"strand":-1,"description":"T-cell-interacting, activating receptor on myeloid cells 1 [Source:HGNC Symbol;Acc:HGNC:37250]"}, {"versioned_ensembl_gene_id":"ENSG00000263479.2","gene_symbol":"RN7SL509P","gene_name":"RNA, 7SL, cytoplasmic 509, pseudogene [Source:HGNC Symbol;Acc:HGNC:46525]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479409","summary":null,"start":96914699,"end":96914995,"strand":-1,"description":"RNA, 7SL, cytoplasmic 509, pseudogene [Source:HGNC Symbol;Acc:HGNC:46525]"}, {"versioned_ensembl_gene_id":"ENSG00000264128.2","gene_symbol":"RN7SL713P","gene_name":"RNA, 7SL, cytoplasmic 713, pseudogene [Source:HGNC Symbol;Acc:HGNC:46729]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480381","summary":null,"start":58565631,"end":58565932,"strand":-1,"description":"RNA, 7SL, cytoplasmic 713, pseudogene [Source:HGNC Symbol;Acc:HGNC:46729]"}, {"versioned_ensembl_gene_id":"ENSG00000201583.1","gene_symbol":"RN7SKP191","gene_name":"RNA, 7SK small nuclear pseudogene 191 [Source:HGNC Symbol;Acc:HGNC:45915]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480471","summary":null,"start":105096756,"end":105097061,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 191 [Source:HGNC Symbol;Acc:HGNC:45915]"}, {"versioned_ensembl_gene_id":"ENSG00000223117.1","gene_symbol":"RN7SKP296","gene_name":"RNA, 7SK small nuclear pseudogene 296 [Source:HGNC Symbol;Acc:HGNC:46020]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481823","summary":null,"start":190642163,"end":190642503,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 296 [Source:HGNC Symbol;Acc:HGNC:46020]"}, {"versioned_ensembl_gene_id":"ENSG00000207129.1","gene_symbol":"RNA5SP187","gene_name":"RNA, 5S ribosomal pseudogene 187 [Source:HGNC Symbol;Acc:HGNC:43087]","synonyms":"RN5S187","biotype":"rRNA","ncbi_id":"100873449","summary":null,"start":88274258,"end":88274376,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 187 [Source:HGNC Symbol;Acc:HGNC:43087]"}, {"versioned_ensembl_gene_id":"ENSG00000274732.1","gene_symbol":"LINC00901","gene_name":"Non-coding RNA BC040587 [Source:RFAM;Acc:RF01884]","synonyms":"LSAMP-AS4,BC040587,TCONS_00005428","biotype":"misc_RNA","ncbi_id":"100506724","summary":null,"start":116921328,"end":116921479,"strand":1,"description":"Non-coding RNA BC040587 [Source:RFAM;Acc:RF01884]"}, {"versioned_ensembl_gene_id":"ENSG00000276065.4","gene_symbol":"GP6","gene_name":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]","synonyms":"GPVI,GPVI","biotype":"protein_coding","ncbi_id":"51206","summary":"This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":55046861,"end":55071420,"strand":-1,"description":"glycoprotein VI platelet [Source:HGNC Symbol;Acc:HGNC:14388]"}, {"versioned_ensembl_gene_id":"ENSG00000199713.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":58818883,"end":58819016,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000277025.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000222312.1","gene_symbol":"RNA5SP178","gene_name":"RNA, 5S ribosomal pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:43078]","synonyms":"RN5S178","biotype":"rRNA","ncbi_id":"100873440","summary":null,"start":16033229,"end":16033356,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:43078]"}, {"versioned_ensembl_gene_id":"ENSG00000207164.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28901236,"end":28901347,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266553.2","gene_symbol":"RN7SL356P","gene_name":"RNA, 7SL, cytoplasmic 356, pseudogene [Source:HGNC Symbol;Acc:HGNC:46372]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479353","summary":null,"start":76967518,"end":76967765,"strand":-1,"description":"RNA, 7SL, cytoplasmic 356, pseudogene [Source:HGNC Symbol;Acc:HGNC:46372]"}, {"versioned_ensembl_gene_id":"ENSG00000201581.1","gene_symbol":"RN7SKP78","gene_name":"RNA, 7SK small nuclear pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:45802]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479129","summary":null,"start":6149623,"end":6149940,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 78 [Source:HGNC Symbol;Acc:HGNC:45802]"}, {"versioned_ensembl_gene_id":"ENSG00000241625.3","gene_symbol":"RN7SL18P","gene_name":"RNA, 7SL, cytoplasmic 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46034]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480927","summary":null,"start":62491178,"end":62491468,"strand":1,"description":"RNA, 7SL, cytoplasmic 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:46034]"}, {"versioned_ensembl_gene_id":"ENSG00000252459.1","gene_symbol":"SNORA27","gene_name":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]","synonyms":"ACA27","biotype":"snoRNA","ncbi_id":"619499","summary":null,"start":114737704,"end":114737798,"strand":1,"description":"Small nucleolar RNA SNORA27 [Source:RFAM;Acc:RF00443]"}, {"versioned_ensembl_gene_id":"ENSG00000201860.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":191641135,"end":191641237,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212347.2","gene_symbol":"SNORD77","gene_name":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692197","summary":null,"start":45892912,"end":45892979,"strand":-1,"description":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]"}, {"versioned_ensembl_gene_id":"ENSG00000272536.2","gene_symbol":"RN7SL840P","gene_name":"RNA, 7SL, cytoplasmic 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:46856]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479528","summary":null,"start":72582803,"end":72583086,"strand":1,"description":"RNA, 7SL, cytoplasmic 840, pseudogene [Source:HGNC Symbol;Acc:HGNC:46856]"}, {"versioned_ensembl_gene_id":"ENSG00000275798.4","gene_symbol":"BTNL2","gene_name":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]","synonyms":"HSBLMHC1,BTL-II,BTN7,BTN7,HSBLMHC1,BTL-II","biotype":"protein_coding","ncbi_id":"56244","summary":"This gene encodes a major histocompatibility complex, class II associated, type I transmembrane protein which belongs to the butyrophilin-like B7 family of immunoregulators. It is thought to be involved in immune surveillance, serving as a negative T-cell regulator by decreasing T-cell proliferation and cytokine release. The encoded protein contains an N-terminal signal peptide, two pairs of immunoglobulin-like domains, separated by a heptad peptide sequence, and a C-terminal transmembrane domain. Naturally occurring mutations in this gene are associated with sarcoidosis, rheumatoid arthritis, ulcerative colitis, inflammatory bowel disease, myositis, type 1 diabetes, systemic lupus erythematosus, acute coronary syndrome, and prostate cancer. [provided by RefSeq, May 2017]","start":32402558,"end":32414973,"strand":-1,"description":"butyrophilin like 2 [Source:HGNC Symbol;Acc:HGNC:1142]"}, {"versioned_ensembl_gene_id":"ENSG00000251735.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":46960423,"end":46960546,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000251818.1","gene_symbol":"SCARNA20","gene_name":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]","synonyms":"ACA66","biotype":"scaRNA","ncbi_id":"677681","summary":null,"start":28018770,"end":28018907,"strand":1,"description":"Small Cajal body specific RNA 20 [Source:RFAM;Acc:RF00601]"}, {"versioned_ensembl_gene_id":"ENSG00000277900.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97081674,"end":97081956,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000202343.1","gene_symbol":"SNORA2","gene_name":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":149594625,"end":149594759,"strand":1,"description":"Small nucleolar RNA SNORA2/SNORA34 family [Source:RFAM;Acc:RF00410]"}, {"versioned_ensembl_gene_id":"ENSG00000202172.1","gene_symbol":"RNU6-1327P","gene_name":"RNA, U6 small nuclear 1327, pseudogene [Source:HGNC Symbol;Acc:HGNC:48290]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481599","summary":null,"start":558826,"end":558930,"strand":1,"description":"RNA, U6 small nuclear 1327, pseudogene [Source:HGNC Symbol;Acc:HGNC:48290]"}, {"versioned_ensembl_gene_id":"ENSG00000206786.1","gene_symbol":"RNU6-701P","gene_name":"RNA, U6 small nuclear 701, pseudogene [Source:HGNC Symbol;Acc:HGNC:47664]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481402","summary":null,"start":119138859,"end":119138965,"strand":1,"description":"RNA, U6 small nuclear 701, pseudogene [Source:HGNC Symbol;Acc:HGNC:47664]"}, {"versioned_ensembl_gene_id":"ENSG00000283791.1","gene_symbol":"MIR612","gene_name":"microRNA 612 [Source:HGNC Symbol;Acc:HGNC:32868]","synonyms":"MIRN612,hsa-mir-612","biotype":"miRNA","ncbi_id":"693197","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65444458,"end":65444557,"strand":1,"description":"microRNA 612 [Source:HGNC Symbol;Acc:HGNC:32868]"}, {"versioned_ensembl_gene_id":"ENSG00000222257.1","gene_symbol":"RN7SKP199","gene_name":"RNA, 7SK small nuclear pseudogene 199 [Source:HGNC Symbol;Acc:HGNC:45923]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479184","summary":null,"start":45995119,"end":45995423,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 199 [Source:HGNC Symbol;Acc:HGNC:45923]"}, {"versioned_ensembl_gene_id":"ENSG00000257770.5","gene_symbol":"GPX5","gene_name":"glutathione peroxidase 5 [Source:HGNC Symbol;Acc:HGNC:4557]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2880","summary":"This gene belongs to the glutathione peroxidase family. It is specifically expressed in the epididymis in the mammalian male reproductive tract, and is androgen-regulated. Unlike several other characterized glutathione peroxidases, this enzyme is not a selenoprotein, lacking the selenocysteine residue. Thus, it is selenium-independent, and has been proposed to play a role in protecting the membranes of spermatozoa from the damaging effects of lipid peroxidation and/or preventing premature acrosome reaction. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2016]","start":28526012,"end":28534951,"strand":1,"description":"glutathione peroxidase 5 [Source:HGNC Symbol;Acc:HGNC:4557]"}, {"versioned_ensembl_gene_id":"ENSG00000202082.2","gene_symbol":"RNU6-290P","gene_name":"RNA, U6 small nuclear 290, pseudogene [Source:HGNC Symbol;Acc:HGNC:47253]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481270","summary":null,"start":126553302,"end":126553402,"strand":-1,"description":"RNA, U6 small nuclear 290, pseudogene [Source:HGNC Symbol;Acc:HGNC:47253]"}, {"versioned_ensembl_gene_id":"ENSG00000243704.3","gene_symbol":"RN7SL105P","gene_name":"RNA, 7SL, cytoplasmic 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:46121]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480487","summary":null,"start":1604374,"end":1604672,"strand":-1,"description":"RNA, 7SL, cytoplasmic 105, pseudogene [Source:HGNC Symbol;Acc:HGNC:46121]"}, {"versioned_ensembl_gene_id":"ENSG00000283998.1","gene_symbol":"MIR492","gene_name":"microRNA 492 [Source:HGNC Symbol;Acc:HGNC:32081]","synonyms":"MIRN492,hsa-mir-492","biotype":"miRNA","ncbi_id":"574449","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":94834398,"end":94834513,"strand":1,"description":"microRNA 492 [Source:HGNC Symbol;Acc:HGNC:32081]"}, {"versioned_ensembl_gene_id":"ENSG00000206641.1","gene_symbol":"RNU6-449P","gene_name":"RNA, U6 small nuclear 449, pseudogene [Source:HGNC Symbol;Acc:HGNC:47412]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481896","summary":null,"start":53764204,"end":53764310,"strand":1,"description":"RNA, U6 small nuclear 449, pseudogene [Source:HGNC Symbol;Acc:HGNC:47412]"}, {"versioned_ensembl_gene_id":"ENSG00000221479.3","gene_symbol":"MIR1251","gene_name":"microRNA 1251 [Source:HGNC Symbol;Acc:HGNC:35317]","synonyms":"MIRN1251,hsa-mir-1251","biotype":"miRNA","ncbi_id":"100302289","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":97491909,"end":97491978,"strand":1,"description":"microRNA 1251 [Source:HGNC Symbol;Acc:HGNC:35317]"}, {"versioned_ensembl_gene_id":"ENSG00000283768.1","gene_symbol":"MIR1178","gene_name":"microRNA 1178 [Source:HGNC Symbol;Acc:HGNC:35259]","synonyms":"MIRN1178,hsa-mir-1178","biotype":"miRNA","ncbi_id":"100302274","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":119713634,"end":119713724,"strand":-1,"description":"microRNA 1178 [Source:HGNC Symbol;Acc:HGNC:35259]"}, {"versioned_ensembl_gene_id":"ENSG00000239356.3","gene_symbol":"RN7SL309P","gene_name":"RNA, 7SL, cytoplasmic 309, pseudogene [Source:HGNC Symbol;Acc:HGNC:46325]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481007","summary":null,"start":65695552,"end":65695837,"strand":1,"description":"RNA, 7SL, cytoplasmic 309, pseudogene [Source:HGNC Symbol;Acc:HGNC:46325]"}, {"versioned_ensembl_gene_id":"ENSG00000207781.1","gene_symbol":"MIR625","gene_name":"microRNA 625 [Source:HGNC Symbol;Acc:HGNC:32881]","synonyms":"MIRN625,hsa-mir-625","biotype":"miRNA","ncbi_id":"693210","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":65471102,"end":65471186,"strand":1,"description":"microRNA 625 [Source:HGNC Symbol;Acc:HGNC:32881]"}, {"versioned_ensembl_gene_id":"ENSG00000200411.1","gene_symbol":"RNA5SP346","gene_name":"RNA, 5S ribosomal pseudogene 346 [Source:HGNC Symbol;Acc:HGNC:43246]","synonyms":"RN5S346","biotype":"rRNA","ncbi_id":"100873608","summary":null,"start":96474572,"end":96474692,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 346 [Source:HGNC Symbol;Acc:HGNC:43246]"}, {"versioned_ensembl_gene_id":"ENSG00000221656.1","gene_symbol":"MIR1225","gene_name":"microRNA 1225 [Source:HGNC Symbol;Acc:HGNC:33931]","synonyms":"MIRN1225,hsa-mir-1225","biotype":"miRNA","ncbi_id":"100188847","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2090195,"end":2090284,"strand":-1,"description":"microRNA 1225 [Source:HGNC Symbol;Acc:HGNC:33931]"}, {"versioned_ensembl_gene_id":"ENSG00000200084.1","gene_symbol":"SNORD68","gene_name":"small nucleolar RNA, C/D box 68 [Source:HGNC Symbol;Acc:HGNC:32729]","synonyms":"HBII-202","biotype":"snoRNA","ncbi_id":"606500","summary":null,"start":89561434,"end":89561517,"strand":1,"description":"small nucleolar RNA, C/D box 68 [Source:HGNC Symbol;Acc:HGNC:32729]"}, {"versioned_ensembl_gene_id":"ENSG00000210709.1","gene_symbol":"RNU6ATAC3P","gene_name":"RNA, U6atac small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34093]","synonyms":null,"biotype":"snRNA","ncbi_id":"100151686","summary":null,"start":46921124,"end":46921249,"strand":1,"description":"RNA, U6atac small nuclear 3, pseudogene [Source:HGNC Symbol;Acc:HGNC:34093]"}, {"versioned_ensembl_gene_id":"ENSG00000252271.1","gene_symbol":"RNU6-1110P","gene_name":"RNA, U6 small nuclear 1110, pseudogene [Source:HGNC Symbol;Acc:HGNC:48073]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480638","summary":null,"start":58384442,"end":58384542,"strand":-1,"description":"RNA, U6 small nuclear 1110, pseudogene [Source:HGNC Symbol;Acc:HGNC:48073]"}, {"versioned_ensembl_gene_id":"ENSG00000278274.1","gene_symbol":"SNORA61","gene_name":"small nucleolar RNA, H/ACA box 61 [Source:HGNC Symbol;Acc:HGNC:32655]","synonyms":"ACA61","biotype":"snoRNA","ncbi_id":"677838","summary":null,"start":28579764,"end":28579893,"strand":-1,"description":"small nucleolar RNA, H/ACA box 61 [Source:HGNC Symbol;Acc:HGNC:32655]"}, {"versioned_ensembl_gene_id":"ENSG00000278591.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43300041,"end":43300231,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000240233.3","gene_symbol":"RN7SL587P","gene_name":"RNA, 7SL, cytoplasmic 587, pseudogene [Source:HGNC Symbol;Acc:HGNC:46603]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479437","summary":null,"start":77547566,"end":77547846,"strand":-1,"description":"RNA, 7SL, cytoplasmic 587, pseudogene [Source:HGNC Symbol;Acc:HGNC:46603]"}, {"versioned_ensembl_gene_id":"ENSG00000273776.1","gene_symbol":"MIR6126","gene_name":"microRNA 6126 [Source:HGNC Symbol;Acc:HGNC:50099]","synonyms":"hsa-mir-6126","biotype":"miRNA","ncbi_id":"102465134","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3485381,"end":3485469,"strand":-1,"description":"microRNA 6126 [Source:HGNC Symbol;Acc:HGNC:50099]"}, {"versioned_ensembl_gene_id":"ENSG00000252623.1","gene_symbol":"RNA5SP481","gene_name":"RNA, 5S ribosomal pseudogene 481 [Source:HGNC Symbol;Acc:HGNC:43381]","synonyms":"RN5S481","biotype":"rRNA","ncbi_id":"100873723","summary":null,"start":32008351,"end":32008472,"strand":1,"description":"RNA, 5S ribosomal pseudogene 481 [Source:HGNC Symbol;Acc:HGNC:43381]"}, {"versioned_ensembl_gene_id":"ENSG00000284154.1","gene_symbol":"MIR3605","gene_name":"microRNA 3605 [Source:HGNC Symbol;Acc:HGNC:38922]","synonyms":"hsa-mir-3605","biotype":"miRNA","ncbi_id":"100500853","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33332393,"end":33332492,"strand":-1,"description":"microRNA 3605 [Source:HGNC Symbol;Acc:HGNC:38922]"}, {"versioned_ensembl_gene_id":"ENSG00000278581.1","gene_symbol":"MIR6080","gene_name":"microRNA 6080 [Source:HGNC Symbol;Acc:HGNC:50142]","synonyms":"hsa-mir-6080","biotype":"miRNA","ncbi_id":"102464831","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":64780759,"end":64780824,"strand":1,"description":"microRNA 6080 [Source:HGNC Symbol;Acc:HGNC:50142]"}, {"versioned_ensembl_gene_id":"ENSG00000265435.1","gene_symbol":"MIR3121","gene_name":"microRNA 3121 [Source:HGNC Symbol;Acc:HGNC:38259]","synonyms":"hsa-mir-3121","biotype":"miRNA","ncbi_id":"100423032","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":180438314,"end":180438390,"strand":-1,"description":"microRNA 3121 [Source:HGNC Symbol;Acc:HGNC:38259]"}, {"versioned_ensembl_gene_id":"ENSG00000251978.1","gene_symbol":"RNA5SP236","gene_name":"RNA, 5S ribosomal pseudogene 236 [Source:HGNC Symbol;Acc:HGNC:43136]","synonyms":"RN5S236","biotype":"rRNA","ncbi_id":"100873494","summary":null,"start":106781600,"end":106781715,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 236 [Source:HGNC Symbol;Acc:HGNC:43136]"}, {"versioned_ensembl_gene_id":"ENSG00000265210.1","gene_symbol":"MIR4486","gene_name":"microRNA 4486 [Source:HGNC Symbol;Acc:HGNC:41566]","synonyms":"hsa-mir-4486","biotype":"miRNA","ncbi_id":"100616118","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19575310,"end":19575372,"strand":1,"description":"microRNA 4486 [Source:HGNC Symbol;Acc:HGNC:41566]"}, {"versioned_ensembl_gene_id":"ENSG00000275518.1","gene_symbol":"MIR6718","gene_name":"microRNA 6718 [Source:HGNC Symbol;Acc:HGNC:50195]","synonyms":"hsa-mir-6718","biotype":"miRNA","ncbi_id":"102465430","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3885353,"end":3885432,"strand":1,"description":"microRNA 6718 [Source:HGNC Symbol;Acc:HGNC:50195]"}, {"versioned_ensembl_gene_id":"ENSG00000222612.1","gene_symbol":"RNU2-52P","gene_name":"RNA, U2 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48545]","synonyms":null,"biotype":"snRNA","ncbi_id":"107080629","summary":null,"start":41024205,"end":41024394,"strand":1,"description":"RNA, U2 small nuclear 52, pseudogene [Source:HGNC Symbol;Acc:HGNC:48545]"}, {"versioned_ensembl_gene_id":"ENSG00000201790.1","gene_symbol":"RNA5SP189","gene_name":"RNA, 5S ribosomal pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:43089]","synonyms":"RN5S189","biotype":"rRNA","ncbi_id":"100873451","summary":null,"start":105922994,"end":105923108,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 189 [Source:HGNC Symbol;Acc:HGNC:43089]"}, {"versioned_ensembl_gene_id":"ENSG00000263389.1","gene_symbol":"MIR3973","gene_name":"microRNA 3973 [Source:HGNC Symbol;Acc:HGNC:41756]","synonyms":"hsa-mir-3973","biotype":"miRNA","ncbi_id":"100616311","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":36010098,"end":36010204,"strand":1,"description":"microRNA 3973 [Source:HGNC Symbol;Acc:HGNC:41756]"}, {"versioned_ensembl_gene_id":"ENSG00000264402.1","gene_symbol":"MIR548AL","gene_name":"microRNA 548al [Source:HGNC Symbol;Acc:HGNC:41736]","synonyms":"hsa-mir-548al","biotype":"miRNA","ncbi_id":"100616215","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74399237,"end":74399333,"strand":1,"description":"microRNA 548al [Source:HGNC Symbol;Acc:HGNC:41736]"}, {"versioned_ensembl_gene_id":"ENSG00000273768.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":146376807,"end":146376970,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000207861.1","gene_symbol":"MIR520H","gene_name":"microRNA 520h [Source:HGNC Symbol;Acc:HGNC:32125]","synonyms":"MIRN520H,hsa-mir-520h","biotype":"miRNA","ncbi_id":"574493","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53742512,"end":53742599,"strand":1,"description":"microRNA 520h [Source:HGNC Symbol;Acc:HGNC:32125]"}, {"versioned_ensembl_gene_id":"ENSG00000284143.1","gene_symbol":"MIR4700","gene_name":"microRNA 4700 [Source:HGNC Symbol;Acc:HGNC:41806]","synonyms":"hsa-mir-4700","biotype":"miRNA","ncbi_id":"100616329","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120723193,"end":120723266,"strand":1,"description":"microRNA 4700 [Source:HGNC Symbol;Acc:HGNC:41806]"}, {"versioned_ensembl_gene_id":"ENSG00000283471.1","gene_symbol":"MIR6863","gene_name":"microRNA 6863 [Source:HGNC Symbol;Acc:HGNC:49942]","synonyms":"hsa-mir-6863","biotype":"miRNA","ncbi_id":"102466752","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56904264,"end":56904353,"strand":1,"description":"microRNA 6863 [Source:HGNC Symbol;Acc:HGNC:49942]"}, {"versioned_ensembl_gene_id":"ENSG00000264452.1","gene_symbol":"snoZ6","gene_name":"Z6 small nucleolar RNA [Source:RFAM;Acc:RF00285]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":44439035,"end":44439110,"strand":1,"description":"Z6 small nucleolar RNA [Source:RFAM;Acc:RF00285]"}, {"versioned_ensembl_gene_id":"ENSG00000284049.1","gene_symbol":"MIR650","gene_name":"microRNA 650 [Source:HGNC Symbol;Acc:HGNC:32906]","synonyms":"hsa-mir-650,MIRN650","biotype":"miRNA","ncbi_id":"723778","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22822776,"end":22822871,"strand":1,"description":"microRNA 650 [Source:HGNC Symbol;Acc:HGNC:32906]"}, {"versioned_ensembl_gene_id":"ENSG00000264809.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":178484408,"end":178484682,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200558.1","gene_symbol":"RNA5SP429","gene_name":"RNA, 5S ribosomal pseudogene 429 [Source:HGNC Symbol;Acc:HGNC:43329]","synonyms":"RN5S429","biotype":"rRNA","ncbi_id":"106480767","summary":null,"start":68742480,"end":68742588,"strand":1,"description":"RNA, 5S ribosomal pseudogene 429 [Source:HGNC Symbol;Acc:HGNC:43329]"}, {"versioned_ensembl_gene_id":"ENSG00000283364.1","gene_symbol":"MIR451B","gene_name":"microRNA 451b [Source:HGNC Symbol;Acc:HGNC:41655]","synonyms":"hsa-mir-451b","biotype":"miRNA","ncbi_id":"100616273","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28861371,"end":28861438,"strand":1,"description":"microRNA 451b [Source:HGNC Symbol;Acc:HGNC:41655]"}, {"versioned_ensembl_gene_id":"ENSG00000206886.1","gene_symbol":"SNORA70","gene_name":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]","synonyms":"DXS648E,RNU70,U70","biotype":"snoRNA","ncbi_id":"26778","summary":null,"start":81764024,"end":81764156,"strand":1,"description":"Small nucleolar RNA SNORA70 [Source:RFAM;Acc:RF00156]"}, {"versioned_ensembl_gene_id":"ENSG00000211514.1","gene_symbol":"MIR454","gene_name":"microRNA 454 [Source:HGNC Symbol;Acc:HGNC:33137]","synonyms":"MIRN454,hsa-mir-454","biotype":"miRNA","ncbi_id":"768216","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":59137758,"end":59137872,"strand":-1,"description":"microRNA 454 [Source:HGNC Symbol;Acc:HGNC:33137]"}, {"versioned_ensembl_gene_id":"ENSG00000278799.1","gene_symbol":"MIR6823","gene_name":"microRNA 6823 [Source:HGNC Symbol;Acc:HGNC:49952]","synonyms":"hsa-mir-6823","biotype":"miRNA","ncbi_id":"102465494","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48549961,"end":48550021,"strand":-1,"description":"microRNA 6823 [Source:HGNC Symbol;Acc:HGNC:49952]"}, {"versioned_ensembl_gene_id":"ENSG00000221493.1","gene_symbol":"MIR320C1","gene_name":"microRNA 320c-1 [Source:HGNC Symbol;Acc:HGNC:35248]","synonyms":"MIRN320C1,hsa-mir-320c-1","biotype":"miRNA","ncbi_id":"100302135","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21683510,"end":21683597,"strand":1,"description":"microRNA 320c-1 [Source:HGNC Symbol;Acc:HGNC:35248]"}, {"versioned_ensembl_gene_id":"ENSG00000277085.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30056241,"end":30056344,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000284272.1","gene_symbol":"MIR4321","gene_name":"microRNA 4321 [Source:HGNC Symbol;Acc:HGNC:38244]","synonyms":"hsa-mir-4321","biotype":"miRNA","ncbi_id":"100423031","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":2250639,"end":2250718,"strand":1,"description":"microRNA 4321 [Source:HGNC Symbol;Acc:HGNC:38244]"}, {"versioned_ensembl_gene_id":"ENSG00000281426.1","gene_symbol":"MIR548BB","gene_name":"microRNA 548bb [Source:HGNC Symbol;Acc:HGNC:50834]","synonyms":"MI0029321","biotype":"miRNA","ncbi_id":"103504735","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":60617805,"end":60617870,"strand":-1,"description":"microRNA 548bb [Source:HGNC Symbol;Acc:HGNC:50834]"}, {"versioned_ensembl_gene_id":"ENSG00000252798.1","gene_symbol":"SCARNA6","gene_name":"Small Cajal body specific RNA 6 [Source:RFAM;Acc:RF00478]","synonyms":"U88","biotype":"scaRNA","ncbi_id":"677772","summary":null,"start":21587627,"end":21587864,"strand":1,"description":"Small Cajal body specific RNA 6 [Source:RFAM;Acc:RF00478]"}, {"versioned_ensembl_gene_id":"ENSG00000202265.1","gene_symbol":"RNU6-596P","gene_name":"RNA, U6 small nuclear 596, pseudogene [Source:HGNC Symbol;Acc:HGNC:47559]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481369","summary":null,"start":57289552,"end":57289649,"strand":1,"description":"RNA, U6 small nuclear 596, pseudogene [Source:HGNC Symbol;Acc:HGNC:47559]"}, {"versioned_ensembl_gene_id":"ENSG00000273898.1","gene_symbol":"MIR6798","gene_name":"microRNA 6798 [Source:HGNC Symbol;Acc:HGNC:50013]","synonyms":"hsa-mir-6798","biotype":"miRNA","ncbi_id":"102466738","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49009906,"end":49009972,"strand":1,"description":"microRNA 6798 [Source:HGNC Symbol;Acc:HGNC:50013]"}, {"versioned_ensembl_gene_id":"ENSG00000251839.1","gene_symbol":"RNU7-12P","gene_name":"RNA, U7 small nuclear 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:34108]","synonyms":"U7.12,RNU7-100P","biotype":"snRNA","ncbi_id":"100147760","summary":null,"start":27232255,"end":27232316,"strand":-1,"description":"RNA, U7 small nuclear 12 pseudogene [Source:HGNC Symbol;Acc:HGNC:34108]"}, {"versioned_ensembl_gene_id":"ENSG00000265452.1","gene_symbol":"MIR3682","gene_name":"microRNA 3682 [Source:HGNC Symbol;Acc:HGNC:38916]","synonyms":"hsa-mir-3682","biotype":"miRNA","ncbi_id":"100500850","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53849122,"end":53849205,"strand":-1,"description":"microRNA 3682 [Source:HGNC Symbol;Acc:HGNC:38916]"}, {"versioned_ensembl_gene_id":"ENSG00000265924.1","gene_symbol":"MIR5692C1","gene_name":"microRNA 5692c-1 [Source:HGNC Symbol;Acc:HGNC:43506]","synonyms":"hsa-mir-5692c-1","biotype":"miRNA","ncbi_id":"100847082","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":135802985,"end":135803075,"strand":-1,"description":"microRNA 5692c-1 [Source:HGNC Symbol;Acc:HGNC:43506]"}, {"versioned_ensembl_gene_id":"ENSG00000283726.1","gene_symbol":"MIR5193","gene_name":"microRNA 5193 [Source:HGNC Symbol;Acc:HGNC:43534]","synonyms":"hsa-mir-5193","biotype":"miRNA","ncbi_id":"100847079","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":49806137,"end":49806245,"strand":-1,"description":"microRNA 5193 [Source:HGNC Symbol;Acc:HGNC:43534]"}, {"versioned_ensembl_gene_id":"ENSG00000222249.1","gene_symbol":"RNU6-262P","gene_name":"RNA, U6 small nuclear 262, pseudogene [Source:HGNC Symbol;Acc:HGNC:47225]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481261","summary":null,"start":119289562,"end":119289677,"strand":-1,"description":"RNA, U6 small nuclear 262, pseudogene [Source:HGNC Symbol;Acc:HGNC:47225]"}, {"versioned_ensembl_gene_id":"ENSG00000278658.1","gene_symbol":"MIR6826","gene_name":"microRNA 6826 [Source:HGNC Symbol;Acc:HGNC:50001]","synonyms":"hsa-mir-6826","biotype":"miRNA","ncbi_id":"102465496","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129272146,"end":129272243,"strand":1,"description":"microRNA 6826 [Source:HGNC Symbol;Acc:HGNC:50001]"}, {"versioned_ensembl_gene_id":"ENSG00000263926.1","gene_symbol":"MIR4462","gene_name":"microRNA 4462 [Source:HGNC Symbol;Acc:HGNC:41549]","synonyms":"hsa-mir-4462","biotype":"miRNA","ncbi_id":"100616413","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37555365,"end":37555422,"strand":-1,"description":"microRNA 4462 [Source:HGNC Symbol;Acc:HGNC:41549]"}, {"versioned_ensembl_gene_id":"ENSG00000277029.1","gene_symbol":"RNU6-1192P","gene_name":"RNA, U6 small nuclear 1192, pseudogene [Source:HGNC Symbol;Acc:HGNC:48155]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480088","summary":null,"start":36404826,"end":36404932,"strand":-1,"description":"RNA, U6 small nuclear 1192, pseudogene [Source:HGNC Symbol;Acc:HGNC:48155]"}, {"versioned_ensembl_gene_id":"ENSG00000251771.2","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":15962302,"end":15962405,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000207931.1","gene_symbol":"MIR577","gene_name":"microRNA 577 [Source:HGNC Symbol;Acc:HGNC:32833]","synonyms":"MIRN577,hsa-mir-577","biotype":"miRNA","ncbi_id":"693162","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":114656759,"end":114656854,"strand":1,"description":"microRNA 577 [Source:HGNC Symbol;Acc:HGNC:32833]"}, {"versioned_ensembl_gene_id":"ENSG00000265725.1","gene_symbol":"MIR3144","gene_name":"microRNA 3144 [Source:HGNC Symbol;Acc:HGNC:38331]","synonyms":"hsa-mir-3144","biotype":"miRNA","ncbi_id":"100422951","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120015179,"end":120015257,"strand":1,"description":"microRNA 3144 [Source:HGNC Symbol;Acc:HGNC:38331]"}, {"versioned_ensembl_gene_id":"ENSG00000221296.2","gene_symbol":"MIR548T","gene_name":"microRNA 548t [Source:HGNC Symbol;Acc:HGNC:38298]","synonyms":"hsa-mir-548t","biotype":"miRNA","ncbi_id":"100422849","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":173268160,"end":173268233,"strand":1,"description":"microRNA 548t [Source:HGNC Symbol;Acc:HGNC:38298]"}, {"versioned_ensembl_gene_id":"ENSG00000206985.1","gene_symbol":"RNU6-198P","gene_name":"RNA, U6 small nuclear 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:47161]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481239","summary":null,"start":39082589,"end":39082692,"strand":1,"description":"RNA, U6 small nuclear 198, pseudogene [Source:HGNC Symbol;Acc:HGNC:47161]"}, {"versioned_ensembl_gene_id":"ENSG00000207619.1","gene_symbol":"MIR585","gene_name":"microRNA 585 [Source:HGNC Symbol;Acc:HGNC:32841]","synonyms":"MIRN585,hsa-mir-585","biotype":"miRNA","ncbi_id":"693170","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":169263601,"end":169263694,"strand":-1,"description":"microRNA 585 [Source:HGNC Symbol;Acc:HGNC:32841]"}, {"versioned_ensembl_gene_id":"ENSG00000283923.1","gene_symbol":"MIR6132","gene_name":"microRNA 6132 [Source:HGNC Symbol;Acc:HGNC:50272]","synonyms":"hsa-mir-6132","biotype":"miRNA","ncbi_id":"102466616","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":117020211,"end":117020319,"strand":1,"description":"microRNA 6132 [Source:HGNC Symbol;Acc:HGNC:50272]"}, {"versioned_ensembl_gene_id":"ENSG00000274263.1","gene_symbol":"MIR7702","gene_name":"microRNA 7702 [Source:HGNC Symbol;Acc:HGNC:50216]","synonyms":"hsa-mir-7702","biotype":"miRNA","ncbi_id":"102465800","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":111271156,"end":111271214,"strand":-1,"description":"microRNA 7702 [Source:HGNC Symbol;Acc:HGNC:50216]"}, {"versioned_ensembl_gene_id":"ENSG00000278411.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":54868957,"end":54869063,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000275992.1","gene_symbol":"RN7SL327P","gene_name":"RNA, 7SL, cytoplasmic 327, pseudogene [Source:HGNC Symbol;Acc:HGNC:46343]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481012","summary":null,"start":75292706,"end":75292928,"strand":1,"description":"RNA, 7SL, cytoplasmic 327, pseudogene [Source:HGNC Symbol;Acc:HGNC:46343]"}, {"versioned_ensembl_gene_id":"ENSG00000251884.1","gene_symbol":"RNA5SP288","gene_name":"RNA, 5S ribosomal pseudogene 288 [Source:HGNC Symbol;Acc:HGNC:43188]","synonyms":"RN5S288","biotype":"rRNA","ncbi_id":"100873541","summary":null,"start":95142449,"end":95142541,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 288 [Source:HGNC Symbol;Acc:HGNC:43188]"}, {"versioned_ensembl_gene_id":"ENSG00000207814.1","gene_symbol":"MIR147A","gene_name":"microRNA 147a [Source:HGNC Symbol;Acc:HGNC:31534]","synonyms":"MIRN147,MIR147,hsa-mir-147","biotype":"miRNA","ncbi_id":"406939","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":120244979,"end":120245050,"strand":-1,"description":"microRNA 147a [Source:HGNC Symbol;Acc:HGNC:31534]"}, {"versioned_ensembl_gene_id":"ENSG00000264744.1","gene_symbol":"MIR3689C","gene_name":"microRNA 3689c [Source:HGNC Symbol;Acc:HGNC:41816]","synonyms":"hsa-mir-3689c","biotype":"miRNA","ncbi_id":"100616333","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":134849298,"end":134849369,"strand":-1,"description":"microRNA 3689c [Source:HGNC Symbol;Acc:HGNC:41816]"}, {"versioned_ensembl_gene_id":"ENSG00000212232.1","gene_symbol":"SNORD17","gene_name":"small nucleolar RNA, C/D box 17 [Source:HGNC Symbol;Acc:HGNC:32713]","synonyms":"HBI-43","biotype":"snoRNA","ncbi_id":"692086","summary":null,"start":17962710,"end":17962946,"strand":-1,"description":"small nucleolar RNA, C/D box 17 [Source:HGNC Symbol;Acc:HGNC:32713]"}, {"versioned_ensembl_gene_id":"ENSG00000264268.1","gene_symbol":"MIR4767","gene_name":"microRNA 4767 [Source:HGNC Symbol;Acc:HGNC:41548]","synonyms":"hsa-mir-4767","biotype":"miRNA","ncbi_id":"100616467","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":7147860,"end":7147937,"strand":1,"description":"microRNA 4767 [Source:HGNC Symbol;Acc:HGNC:41548]"}, {"versioned_ensembl_gene_id":"ENSG00000251897.1","gene_symbol":"RNU6-916P","gene_name":"RNA, U6 small nuclear 916, pseudogene [Source:HGNC Symbol;Acc:HGNC:47879]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481468","summary":null,"start":6936912,"end":6937020,"strand":-1,"description":"RNA, U6 small nuclear 916, pseudogene [Source:HGNC Symbol;Acc:HGNC:47879]"}, {"versioned_ensembl_gene_id":"ENSG00000212013.1","gene_symbol":"MIR509-2","gene_name":"microRNA 509-2 [Source:HGNC Symbol;Acc:HGNC:33641]","synonyms":"MIRN509-2,hsa-mir-509-2","biotype":"miRNA","ncbi_id":"100126301","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147258760,"end":147258850,"strand":-1,"description":"microRNA 509-2 [Source:HGNC Symbol;Acc:HGNC:33641]"}, {"versioned_ensembl_gene_id":"ENSG00000199402.1","gene_symbol":"RNA5SP308","gene_name":"RNA, 5S ribosomal pseudogene 308 [Source:HGNC Symbol;Acc:HGNC:43208]","synonyms":"RN5S308","biotype":"rRNA","ncbi_id":"100873582","summary":null,"start":28874393,"end":28874507,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 308 [Source:HGNC Symbol;Acc:HGNC:43208]"}, {"versioned_ensembl_gene_id":"ENSG00000241665.3","gene_symbol":"RN7SL418P","gene_name":"RNA, 7SL, cytoplasmic 418, pseudogene [Source:HGNC Symbol;Acc:HGNC:46434]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480508","summary":null,"start":69769487,"end":69769773,"strand":-1,"description":"RNA, 7SL, cytoplasmic 418, pseudogene [Source:HGNC Symbol;Acc:HGNC:46434]"}, {"versioned_ensembl_gene_id":"ENSG00000200345.2","gene_symbol":"RNU6-485P","gene_name":"RNA, U6 small nuclear 485, pseudogene [Source:HGNC Symbol;Acc:HGNC:47448]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481333","summary":null,"start":7118785,"end":7118891,"strand":1,"description":"RNA, U6 small nuclear 485, pseudogene [Source:HGNC Symbol;Acc:HGNC:47448]"}, {"versioned_ensembl_gene_id":"ENSG00000273835.1","gene_symbol":"SNORD115-13","gene_name":"small nucleolar RNA, C/D box 115-13 [Source:HGNC Symbol;Acc:HGNC:33032]","synonyms":"HBII-52-13","biotype":"snoRNA","ncbi_id":"100033450","summary":null,"start":25193321,"end":25193402,"strand":1,"description":"small nucleolar RNA, C/D box 115-13 [Source:HGNC Symbol;Acc:HGNC:33032]"}, {"versioned_ensembl_gene_id":"ENSG00000252414.1","gene_symbol":"RNU6-100P","gene_name":"RNA, U6 small nuclear 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:47063]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481208","summary":null,"start":64578892,"end":64578997,"strand":1,"description":"RNA, U6 small nuclear 100, pseudogene [Source:HGNC Symbol;Acc:HGNC:47063]"}, {"versioned_ensembl_gene_id":"ENSG00000206952.3","gene_symbol":"SNORA50A","gene_name":"small nucleolar RNA, H/ACA box 50A [Source:HGNC Symbol;Acc:HGNC:32643]","synonyms":"SNORA50,ACA50,SNORA76A,SNORA50,ACA50,SNORA76A","biotype":"snoRNA","ncbi_id":"677830","summary":null,"start":58559796,"end":58559929,"strand":-1,"description":"small nucleolar RNA, H/ACA box 50A [Source:HGNC Symbol;Acc:HGNC:32643]"}, {"versioned_ensembl_gene_id":"ENSG00000266716.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31654037,"end":31654150,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278771.1","gene_symbol":"RN7SL3","gene_name":"RNA, 7SL, cytoplasmic 3 [Source:HGNC Symbol;Acc:HGNC:23135]","synonyms":"RNSRP3,RN7SL631P,7L30.2","biotype":"misc_RNA","ncbi_id":"378707","summary":"The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL3, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]","start":49853616,"end":49853914,"strand":-1,"description":"RNA, 7SL, cytoplasmic 3 [Source:HGNC Symbol;Acc:HGNC:23135]"}, {"versioned_ensembl_gene_id":"ENSG00000239185.1","gene_symbol":"RNU7-190P","gene_name":"RNA, U7 small nuclear 190 pseudogene [Source:HGNC Symbol;Acc:HGNC:45724]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479096","summary":null,"start":117139715,"end":117139775,"strand":-1,"description":"RNA, U7 small nuclear 190 pseudogene [Source:HGNC Symbol;Acc:HGNC:45724]"}, {"versioned_ensembl_gene_id":"ENSG00000264391.2","gene_symbol":"RN7SL208P","gene_name":"RNA, 7SL, cytoplasmic 208, pseudogene [Source:HGNC Symbol;Acc:HGNC:46224]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480978","summary":null,"start":76836900,"end":76837195,"strand":-1,"description":"RNA, 7SL, cytoplasmic 208, pseudogene [Source:HGNC Symbol;Acc:HGNC:46224]"}, {"versioned_ensembl_gene_id":"ENSG00000199771.1","gene_symbol":"RNA5SP426","gene_name":"RNA, 5S ribosomal pseudogene 426 [Source:HGNC Symbol;Acc:HGNC:43326]","synonyms":"RN5S426","biotype":"rRNA","ncbi_id":"100873677","summary":null,"start":50869455,"end":50869575,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 426 [Source:HGNC Symbol;Acc:HGNC:43326]"}, {"versioned_ensembl_gene_id":"ENSG00000274228.1","gene_symbol":"RNA5SP414","gene_name":"RNA, 5S ribosomal pseudogene 414 [Source:HGNC Symbol;Acc:HGNC:43314]","synonyms":"RN5S414","biotype":"rRNA","ncbi_id":"100873665","summary":null,"start":35748520,"end":35748655,"strand":1,"description":"RNA, 5S ribosomal pseudogene 414 [Source:HGNC Symbol;Acc:HGNC:43314]"}, {"versioned_ensembl_gene_id":"ENSG00000207432.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30112198,"end":30112330,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000275971.1","gene_symbol":"RMST_6","gene_name":"Rhabdomyosarcoma 2 associated transcript conserved region 6 [Source:RFAM;Acc:RF01967]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":97530656,"end":97530858,"strand":1,"description":"Rhabdomyosarcoma 2 associated transcript conserved region 6 [Source:RFAM;Acc:RF01967]"}, {"versioned_ensembl_gene_id":"ENSG00000200063.1","gene_symbol":"SNORA30","gene_name":"Small nucleolar RNA SNORA30/SNORA37 family [Source:RFAM;Acc:RF00415]","synonyms":"SNORA30A,ACA30","biotype":"snoRNA","ncbi_id":"677813","summary":null,"start":78399935,"end":78400063,"strand":1,"description":"Small 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The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":122146522,"end":122146593,"strand":-1,"description":"microRNA let-7a-2 [Source:HGNC Symbol;Acc:HGNC:31477]"}, {"versioned_ensembl_gene_id":"ENSG00000283759.1","gene_symbol":"MIR614","gene_name":"microRNA 614 [Source:HGNC Symbol;Acc:HGNC:32870]","synonyms":"MIRN614,hsa-mir-614","biotype":"miRNA","ncbi_id":"693199","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12915829,"end":12915918,"strand":1,"description":"microRNA 614 [Source:HGNC Symbol;Acc:HGNC:32870]"}, {"versioned_ensembl_gene_id":"ENSG00000264916.2","gene_symbol":"RN7SL230P","gene_name":"RNA, 7SL, cytoplasmic 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:46246]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479306","summary":null,"start":179900262,"end":179900564,"strand":1,"description":"RNA, 7SL, cytoplasmic 230, pseudogene [Source:HGNC Symbol;Acc:HGNC:46246]"}, {"versioned_ensembl_gene_id":"ENSG00000284011.1","gene_symbol":"MIR6502","gene_name":"microRNA 6502 [Source:HGNC Symbol;Acc:HGNC:50062]","synonyms":"hsa-mir-6502","biotype":"miRNA","ncbi_id":"102465249","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":66251082,"end":66251157,"strand":1,"description":"microRNA 6502 [Source:HGNC Symbol;Acc:HGNC:50062]"}, {"versioned_ensembl_gene_id":"ENSG00000277455.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":24449351,"end":24449615,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000200150.1","gene_symbol":"SNORD113","gene_name":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":100956240,"end":100956312,"strand":1,"description":"Small nucleolar RNA SNORD113/SNORD114 family [Source:RFAM;Acc:RF00181]"}, {"versioned_ensembl_gene_id":"ENSG00000239151.1","gene_symbol":"RNU7-195P","gene_name":"RNA, U7 small nuclear 195 pseudogene [Source:HGNC Symbol;Acc:HGNC:45729]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479097","summary":null,"start":89120779,"end":89120840,"strand":1,"description":"RNA, U7 small nuclear 195 pseudogene [Source:HGNC Symbol;Acc:HGNC:45729]"}, {"versioned_ensembl_gene_id":"ENSG00000207087.1","gene_symbol":"RNU6-242P","gene_name":"RNA, U6 small nuclear 242, pseudogene [Source:HGNC Symbol;Acc:HGNC:47205]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481254","summary":null,"start":43091388,"end":43091494,"strand":-1,"description":"RNA, U6 small nuclear 242, pseudogene [Source:HGNC Symbol;Acc:HGNC:47205]"}, {"versioned_ensembl_gene_id":"ENSG00000244632.3","gene_symbol":"RN7SL863P","gene_name":"RNA, 7SL, cytoplasmic 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:46879]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480538","summary":null,"start":62796124,"end":62796419,"strand":-1,"description":"RNA, 7SL, cytoplasmic 863, pseudogene [Source:HGNC Symbol;Acc:HGNC:46879]"}, {"versioned_ensembl_gene_id":"ENSG00000277919.1","gene_symbol":"MIR8067","gene_name":"microRNA 8067 [Source:HGNC Symbol;Acc:HGNC:49934]","synonyms":"hsa-mir-8067","biotype":"miRNA","ncbi_id":"102465869","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":62304658,"end":62304734,"strand":-1,"description":"microRNA 8067 [Source:HGNC Symbol;Acc:HGNC:49934]"}, {"versioned_ensembl_gene_id":"ENSG00000207451.1","gene_symbol":"RNU6-291P","gene_name":"RNA, U6 small nuclear 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:47254]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479696","summary":null,"start":11226254,"end":11226360,"strand":1,"description":"RNA, U6 small nuclear 291, pseudogene [Source:HGNC Symbol;Acc:HGNC:47254]"}, {"versioned_ensembl_gene_id":"ENSG00000199156.1","gene_symbol":"MIR422A","gene_name":"microRNA 422a [Source:HGNC Symbol;Acc:HGNC:31879]","synonyms":"MIRN422A,hsa-mir-422a","biotype":"miRNA","ncbi_id":"494334","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63870930,"end":63871019,"strand":-1,"description":"microRNA 422a [Source:HGNC Symbol;Acc:HGNC:31879]"}, {"versioned_ensembl_gene_id":"ENSG00000199911.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":24910594,"end":24910695,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000265503.1","gene_symbol":"MIR1269B","gene_name":"microRNA 1269b [Source:HGNC Symbol;Acc:HGNC:41787]","synonyms":"hsa-mir-1269b","biotype":"miRNA","ncbi_id":"100616494","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12917268,"end":12917342,"strand":-1,"description":"microRNA 1269b [Source:HGNC Symbol;Acc:HGNC:41787]"}, {"versioned_ensembl_gene_id":"ENSG00000276034.1","gene_symbol":"ZNRD1-AS1_3","gene_name":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30050976,"end":30051079,"strand":1,"description":"ZNRD1 antisense RNA 1 conserved region 3 [Source:RFAM;Acc:RF02220]"}, {"versioned_ensembl_gene_id":"ENSG00000201741.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":17460444,"end":17460522,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000263583.1","gene_symbol":"MIR4522","gene_name":"microRNA 4522 [Source:HGNC Symbol;Acc:HGNC:41668]","synonyms":"hsa-mir-4522","biotype":"miRNA","ncbi_id":"100616277","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":27293910,"end":27293996,"strand":-1,"description":"microRNA 4522 [Source:HGNC Symbol;Acc:HGNC:41668]"}, {"versioned_ensembl_gene_id":"ENSG00000263800.1","gene_symbol":"MIR5684","gene_name":"microRNA 5684 [Source:HGNC Symbol;Acc:HGNC:43544]","synonyms":"hsa-mir-5684","biotype":"miRNA","ncbi_id":"100847071","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12787128,"end":12787192,"strand":1,"description":"microRNA 5684 [Source:HGNC Symbol;Acc:HGNC:43544]"}, {"versioned_ensembl_gene_id":"ENSG00000252989.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"ACA31,SNORA31A","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":100646121,"end":100646197,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000199609.1","gene_symbol":"RNA5SP124","gene_name":"RNA, 5S ribosomal pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:43024]","synonyms":"RN5S124","biotype":"rRNA","ncbi_id":"100873394","summary":null,"start":14394648,"end":14394757,"strand":1,"description":"RNA, 5S ribosomal pseudogene 124 [Source:HGNC Symbol;Acc:HGNC:43024]"}, {"versioned_ensembl_gene_id":"ENSG00000264393.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31845835,"end":31845923,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206927.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":18397937,"end":18398036,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199797.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":28303754,"end":28303850,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000241652.3","gene_symbol":"RN7SL253P","gene_name":"RNA, 7SL, cytoplasmic 253, pseudogene [Source:HGNC Symbol;Acc:HGNC:46269]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479314","summary":null,"start":173141643,"end":173141938,"strand":1,"description":"RNA, 7SL, cytoplasmic 253, pseudogene [Source:HGNC Symbol;Acc:HGNC:46269]"}, {"versioned_ensembl_gene_id":"ENSG00000252317.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":240341385,"end":240341477,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264279.1","gene_symbol":"MIR4786","gene_name":"microRNA 4786 [Source:HGNC Symbol;Acc:HGNC:41751]","synonyms":"hsa-mir-4786","biotype":"miRNA","ncbi_id":"100616417","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":239943015,"end":239943094,"strand":-1,"description":"microRNA 4786 [Source:HGNC Symbol;Acc:HGNC:41751]"}, {"versioned_ensembl_gene_id":"ENSG00000283320.1","gene_symbol":"MIR103B2","gene_name":"microRNA 103b-2 [Source:HGNC Symbol;Acc:HGNC:35385]","synonyms":"MIRN103-2AS,MIR103-2AS,hsa-mir-103b-2,hsa-mir-103-2-as","biotype":"miRNA","ncbi_id":"100302282","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":3917502,"end":3917563,"strand":-1,"description":"microRNA 103b-2 [Source:HGNC Symbol;Acc:HGNC:35385]"}, {"versioned_ensembl_gene_id":"ENSG00000272262.1","gene_symbol":"RNU6-89P","gene_name":"RNA, U6 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:47052]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480550","summary":null,"start":202410108,"end":202410207,"strand":-1,"description":"RNA, U6 small nuclear 89, pseudogene [Source:HGNC Symbol;Acc:HGNC:47052]"}, {"versioned_ensembl_gene_id":"ENSG00000207554.1","gene_symbol":"MIR647","gene_name":"microRNA 647 [Source:HGNC Symbol;Acc:HGNC:32903]","synonyms":"MIRN647,hsa-mir-647","biotype":"miRNA","ncbi_id":"693232","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63942631,"end":63942726,"strand":-1,"description":"microRNA 647 [Source:HGNC Symbol;Acc:HGNC:32903]"}, {"versioned_ensembl_gene_id":"ENSG00000266243.1","gene_symbol":"MIR4279","gene_name":"microRNA 4279 [Source:HGNC Symbol;Acc:HGNC:38195]","synonyms":"hsa-mir-4279","biotype":"miRNA","ncbi_id":"100422874","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31936102,"end":31936159,"strand":-1,"description":"microRNA 4279 [Source:HGNC Symbol;Acc:HGNC:38195]"}, {"versioned_ensembl_gene_id":"ENSG00000264760.1","gene_symbol":"MIR3141","gene_name":"microRNA 3141 [Source:HGNC Symbol;Acc:HGNC:38326]","synonyms":"hsa-mir-3141","biotype":"miRNA","ncbi_id":"100422950","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":154596012,"end":154596072,"strand":-1,"description":"microRNA 3141 [Source:HGNC Symbol;Acc:HGNC:38326]"}, {"versioned_ensembl_gene_id":"ENSG00000202027.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":155120490,"end":155120598,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284446.1","gene_symbol":"MIR1236","gene_name":"microRNA 1236 [Source:HGNC Symbol;Acc:HGNC:33925]","synonyms":"MIRN1236,hsa-mir-1236","biotype":"miRNA","ncbi_id":"100302242","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31956839,"end":31956940,"strand":-1,"description":"microRNA 1236 [Source:HGNC Symbol;Acc:HGNC:33925]"}, {"versioned_ensembl_gene_id":"ENSG00000241392.3","gene_symbol":"RN7SL205P","gene_name":"RNA, 7SL, cytoplasmic 205, pseudogene [Source:HGNC Symbol;Acc:HGNC:46221]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479297","summary":null,"start":131720260,"end":131720543,"strand":-1,"description":"RNA, 7SL, cytoplasmic 205, pseudogene [Source:HGNC Symbol;Acc:HGNC:46221]"}, {"versioned_ensembl_gene_id":"ENSG00000199321.1","gene_symbol":"SNORD60","gene_name":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]","synonyms":"U60,RNU60","biotype":"snoRNA","ncbi_id":"26788","summary":null,"start":126779702,"end":126779774,"strand":-1,"description":"Small nucleolar RNA SNORD60 [Source:RFAM;Acc:RF00271]"}, {"versioned_ensembl_gene_id":"ENSG00000207632.1","gene_symbol":"MIR588","gene_name":"microRNA 588 [Source:HGNC Symbol;Acc:HGNC:32844]","synonyms":"MIRN588,hsa-mir-588","biotype":"miRNA","ncbi_id":"693173","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":126484631,"end":126484713,"strand":1,"description":"microRNA 588 [Source:HGNC Symbol;Acc:HGNC:32844]"}, {"versioned_ensembl_gene_id":"ENSG00000252915.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":39344537,"end":39344628,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000264069.3","gene_symbol":"MIR3943","gene_name":"microRNA 3943 [Source:HGNC Symbol;Acc:HGNC:38888]","synonyms":"hsa-mir-3943","biotype":"miRNA","ncbi_id":"100500829","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43150895,"end":43150994,"strand":1,"description":"microRNA 3943 [Source:HGNC Symbol;Acc:HGNC:38888]"}, {"versioned_ensembl_gene_id":"ENSG00000199043.1","gene_symbol":"MIR335","gene_name":"microRNA 335 [Source:HGNC Symbol;Acc:HGNC:31773]","synonyms":"MIRN335,hsa-mir-335","biotype":"miRNA","ncbi_id":"442904","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The encoded miRNA is dysregulated in a variety of cancers, including breast, colorectal, and prostate cancer. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2017]","start":130496111,"end":130496204,"strand":1,"description":"microRNA 335 [Source:HGNC Symbol;Acc:HGNC:31773]"}, {"versioned_ensembl_gene_id":"ENSG00000284200.1","gene_symbol":"MIR6847","gene_name":"microRNA 6847 [Source:HGNC Symbol;Acc:HGNC:50022]","synonyms":"hsa-mir-6847","biotype":"miRNA","ncbi_id":"102465510","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":144079874,"end":144079942,"strand":1,"description":"microRNA 6847 [Source:HGNC Symbol;Acc:HGNC:50022]"}, {"versioned_ensembl_gene_id":"ENSG00000277079.3","gene_symbol":"RPS9","gene_name":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]","synonyms":"S9,S9","biotype":"protein_coding","ncbi_id":"6203","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S4P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. As is typical for genes encoding ribosomal proteins, multiple processed pseudogenes derived from this gene are dispersed through the genome. [provided by RefSeq, Jul 2008]","start":54201473,"end":54208260,"strand":1,"description":"ribosomal protein S9 [Source:HGNC Symbol;Acc:HGNC:10442]"}, {"versioned_ensembl_gene_id":"ENSG00000276029.1","gene_symbol":"MIR4477A","gene_name":"microRNA 4477a [Source:HGNC Symbol;Acc:HGNC:41859]","synonyms":"hsa-mir-4477a","biotype":"miRNA","ncbi_id":"100616184","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41233755,"end":41233835,"strand":1,"description":"microRNA 4477a [Source:HGNC Symbol;Acc:HGNC:41859]"}, {"versioned_ensembl_gene_id":"ENSG00000202470.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":95275770,"end":95275872,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000240927.3","gene_symbol":"RN7SL209P","gene_name":"RNA, 7SL, cytoplasmic 209, pseudogene [Source:HGNC Symbol;Acc:HGNC:46225]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480494","summary":null,"start":101773238,"end":101773513,"strand":-1,"description":"RNA, 7SL, cytoplasmic 209, pseudogene [Source:HGNC Symbol;Acc:HGNC:46225]"}, {"versioned_ensembl_gene_id":"ENSG00000251809.1","gene_symbol":"RN7SKP14","gene_name":"RNA, 7SK small nuclear pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:45738]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479101","summary":null,"start":54770949,"end":54771277,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:45738]"}, {"versioned_ensembl_gene_id":"ENSG00000201666.1","gene_symbol":"SNORD74","gene_name":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]","synonyms":null,"biotype":"snoRNA","ncbi_id":"619498","summary":null,"start":28924069,"end":28924138,"strand":1,"description":"Small nucleolar RNA SNORD74 [Source:RFAM;Acc:RF00284]"}, {"versioned_ensembl_gene_id":"ENSG00000207617.4","gene_symbol":"MIR3074","gene_name":"microRNA 3074 [Source:HGNC Symbol;Acc:HGNC:38268]","synonyms":"hsa-mir-3074","biotype":"miRNA","ncbi_id":"100422842","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":95086014,"end":95086094,"strand":-1,"description":"microRNA 3074 [Source:HGNC Symbol;Acc:HGNC:38268]"}, {"versioned_ensembl_gene_id":"ENSG00000277889.1","gene_symbol":"MIR8081","gene_name":"microRNA 8081 [Source:HGNC Symbol;Acc:HGNC:50123]","synonyms":"hsa-mir-8081","biotype":"miRNA","ncbi_id":"102465995","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":106600928,"end":106601022,"strand":1,"description":"microRNA 8081 [Source:HGNC Symbol;Acc:HGNC:50123]"}, {"versioned_ensembl_gene_id":"ENSG00000202497.1","gene_symbol":"RNU6-898P","gene_name":"RNA, U6 small nuclear 898, pseudogene [Source:HGNC Symbol;Acc:HGNC:47861]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481462","summary":null,"start":69007052,"end":69007155,"strand":-1,"description":"RNA, U6 small nuclear 898, pseudogene [Source:HGNC Symbol;Acc:HGNC:47861]"}, {"versioned_ensembl_gene_id":"ENSG00000207693.1","gene_symbol":"MIR602","gene_name":"microRNA 602 [Source:HGNC Symbol;Acc:HGNC:32858]","synonyms":"MIRN602,hsa-mir-602","biotype":"miRNA","ncbi_id":"693187","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":137838419,"end":137838516,"strand":1,"description":"microRNA 602 [Source:HGNC Symbol;Acc:HGNC:32858]"}, {"versioned_ensembl_gene_id":"ENSG00000207785.1","gene_symbol":"MIR500A","gene_name":"microRNA 500a [Source:HGNC Symbol;Acc:HGNC:32134]","synonyms":"MIRN500,MIR500,hsa-mir-500","biotype":"miRNA","ncbi_id":"574502","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50008431,"end":50008514,"strand":1,"description":"microRNA 500a [Source:HGNC Symbol;Acc:HGNC:32134]"}, {"versioned_ensembl_gene_id":"ENSG00000206782.1","gene_symbol":"RNU6-224P","gene_name":"RNA, U6 small nuclear 224, pseudogene [Source:HGNC Symbol;Acc:HGNC:47187]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479666","summary":null,"start":131273242,"end":131273348,"strand":1,"description":"RNA, U6 small nuclear 224, pseudogene [Source:HGNC Symbol;Acc:HGNC:47187]"}, {"versioned_ensembl_gene_id":"ENSG00000222532.1","gene_symbol":"MIR1468","gene_name":"microRNA 1468 [Source:HGNC Symbol;Acc:HGNC:35250]","synonyms":"MIRN1468,hsa-mir-1468","biotype":"miRNA","ncbi_id":"100302115","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":63786002,"end":63786087,"strand":-1,"description":"microRNA 1468 [Source:HGNC Symbol;Acc:HGNC:35250]"}, {"versioned_ensembl_gene_id":"ENSG00000207866.1","gene_symbol":"MIR514A2","gene_name":"microRNA 514a-2 [Source:HGNC Symbol;Acc:HGNC:32149]","synonyms":"MIRN514-2,MIR514-2,hsa-mir-514-2","biotype":"miRNA","ncbi_id":"574517","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147281943,"end":147282030,"strand":-1,"description":"microRNA 514a-2 [Source:HGNC Symbol;Acc:HGNC:32149]"}, {"versioned_ensembl_gene_id":"ENSG00000212297.1","gene_symbol":"RNU6-821P","gene_name":"RNA, U6 small nuclear 821, pseudogene [Source:HGNC Symbol;Acc:HGNC:47784]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481440","summary":null,"start":198071311,"end":198071417,"strand":-1,"description":"RNA, U6 small nuclear 821, pseudogene [Source:HGNC Symbol;Acc:HGNC:47784]"}, {"versioned_ensembl_gene_id":"ENSG00000206645.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":37093133,"end":37093234,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207072.1","gene_symbol":"RNU6-39P","gene_name":"RNA, U6 small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:34283]","synonyms":"RNU6-39","biotype":"snRNA","ncbi_id":"100873758","summary":null,"start":68858934,"end":68859040,"strand":1,"description":"RNA, U6 small nuclear 39, pseudogene [Source:HGNC Symbol;Acc:HGNC:34283]"}, {"versioned_ensembl_gene_id":"ENSG00000277786.4","gene_symbol":"NLRP7","gene_name":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]","synonyms":"NOD12,PYPAF3,CLR19.4,NOD12,PAN7,CLR19.4,NALP7,PAN7,PYPAF3,NALP7","biotype":"protein_coding","ncbi_id":"199713","summary":"This gene encodes a member of the NACHT, leucine rich repeat, and PYD containing (NLRP) protein family. It has an N-terminal pyrin domain, followed by a NACHT domain, a NACHT-associated domain (NAD), and a C-terminal leucine-rich repeat (LRR) region. NLRP proteins are implicated in the activation of proinflammatory caspases through multiprotein complexes called inflammasomes. This gene may act as a feedback regulator of caspase-1-dependent interleukin 1-beta secretion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":54852540,"end":54876536,"strand":-1,"description":"NLR family pyrin domain containing 7 [Source:HGNC Symbol;Acc:HGNC:22947]"}, {"versioned_ensembl_gene_id":"ENSG00000276193.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":133668420,"end":133668701,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000252424.1","gene_symbol":"RNA5SP384","gene_name":"RNA, 5S ribosomal pseudogene 384 [Source:HGNC Symbol;Acc:HGNC:43284]","synonyms":"RN5S384","biotype":"rRNA","ncbi_id":"100873639","summary":null,"start":49552633,"end":49552748,"strand":1,"description":"RNA, 5S ribosomal pseudogene 384 [Source:HGNC Symbol;Acc:HGNC:43284]"}, {"versioned_ensembl_gene_id":"ENSG00000200683.1","gene_symbol":"RNU6-379P","gene_name":"RNA, U6 small nuclear 379, pseudogene [Source:HGNC Symbol;Acc:HGNC:47342]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479734","summary":null,"start":40917743,"end":40917846,"strand":1,"description":"RNA, U6 small nuclear 379, pseudogene [Source:HGNC Symbol;Acc:HGNC:47342]"}, {"versioned_ensembl_gene_id":"ENSG00000212368.1","gene_symbol":"RNU6-1000P","gene_name":"RNA, U6 small nuclear 1000, pseudogene [Source:HGNC Symbol;Acc:HGNC:47963]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481496","summary":null,"start":76356610,"end":76356715,"strand":-1,"description":"RNA, U6 small nuclear 1000, pseudogene [Source:HGNC Symbol;Acc:HGNC:47963]"}, {"versioned_ensembl_gene_id":"ENSG00000201143.1","gene_symbol":"SNORD115-42","gene_name":"small nucleolar RNA, C/D box 115-42 [Source:HGNC Symbol;Acc:HGNC:33061]","synonyms":"HBII-52-42","biotype":"snoRNA","ncbi_id":"100033816","summary":null,"start":25247345,"end":25247426,"strand":1,"description":"small nucleolar RNA, C/D box 115-42 [Source:HGNC Symbol;Acc:HGNC:33061]"}, {"versioned_ensembl_gene_id":"ENSG00000206799.1","gene_symbol":"SNORA32","gene_name":"small nucleolar RNA, H/ACA box 32 [Source:HGNC Symbol;Acc:HGNC:32622]","synonyms":"ACA32","biotype":"snoRNA","ncbi_id":"692063","summary":null,"start":93730979,"end":93731099,"strand":-1,"description":"small nucleolar RNA, H/ACA box 32 [Source:HGNC Symbol;Acc:HGNC:32622]"}, {"versioned_ensembl_gene_id":"ENSG00000202434.1","gene_symbol":"SNORA4","gene_name":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]","synonyms":"ACA4","biotype":"snoRNA","ncbi_id":"619568","summary":null,"start":197404718,"end":197404854,"strand":1,"description":"Small nucleolar RNA SNORA4 [Source:RFAM;Acc:RF00394]"}, {"versioned_ensembl_gene_id":"ENSG00000241983.3","gene_symbol":"RN7SL566P","gene_name":"RNA, 7SL, cytoplasmic 566, pseudogene [Source:HGNC Symbol;Acc:HGNC:46582]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481850","summary":null,"start":39369153,"end":39369448,"strand":1,"description":"RNA, 7SL, cytoplasmic 566, pseudogene [Source:HGNC Symbol;Acc:HGNC:46582]"}, {"versioned_ensembl_gene_id":"ENSG00000265707.1","gene_symbol":"SNORD52","gene_name":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]","synonyms":"U52,RNU52,U52,RNU52","biotype":"snoRNA","ncbi_id":"26797","summary":null,"start":31819261,"end":31819327,"strand":1,"description":"small nucleolar RNA, C/D box 52 [Source:HGNC Symbol;Acc:HGNC:10202]"}, {"versioned_ensembl_gene_id":"ENSG00000253081.1","gene_symbol":"RNU4ATAC17P","gene_name":"RNA, U4atac small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:46903]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480696","summary":null,"start":8364529,"end":8364648,"strand":-1,"description":"RNA, U4atac small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:46903]"}, {"versioned_ensembl_gene_id":"ENSG00000266231.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":31823970,"end":31824072,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200291.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":117914244,"end":117914345,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252700.1","gene_symbol":"RNU7-110P","gene_name":"RNA, U7 small nuclear 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:45644]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480815","summary":null,"start":33414150,"end":33414211,"strand":1,"description":"RNA, U7 small nuclear 110 pseudogene [Source:HGNC Symbol;Acc:HGNC:45644]"}, {"versioned_ensembl_gene_id":"ENSG00000199426.1","gene_symbol":"RNU1-108P","gene_name":"RNA, U1 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:48450]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481957","summary":null,"start":58666537,"end":58666697,"strand":-1,"description":"RNA, U1 small nuclear 108, pseudogene [Source:HGNC Symbol;Acc:HGNC:48450]"}, {"versioned_ensembl_gene_id":"ENSG00000276568.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":6928345,"end":6928629,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000242998.3","gene_symbol":"RN7SL379P","gene_name":"RNA, 7SL, cytoplasmic 379, pseudogene [Source:HGNC Symbol;Acc:HGNC:46395]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480505","summary":null,"start":96023360,"end":96023652,"strand":1,"description":"RNA, 7SL, cytoplasmic 379, pseudogene [Source:HGNC Symbol;Acc:HGNC:46395]"}, {"versioned_ensembl_gene_id":"ENSG00000206880.1","gene_symbol":"RNU6-1310P","gene_name":"RNA, U6 small nuclear 1310, pseudogene [Source:HGNC Symbol;Acc:HGNC:48273]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480658","summary":null,"start":168263375,"end":168263481,"strand":-1,"description":"RNA, U6 small nuclear 1310, pseudogene [Source:HGNC Symbol;Acc:HGNC:48273]"}, {"versioned_ensembl_gene_id":"ENSG00000266802.1","gene_symbol":"MIR4419A","gene_name":"microRNA 4419a [Source:HGNC Symbol;Acc:HGNC:41828]","synonyms":"hsa-mir-4419a","biotype":"miRNA","ncbi_id":"100616177","summary":"This record was withdrawn by miRBase.","start":23057858,"end":23057934,"strand":-1,"description":"microRNA 4419a [Source:HGNC Symbol;Acc:HGNC:41828]"}, {"versioned_ensembl_gene_id":"ENSG00000275207.1","gene_symbol":"MIR6740","gene_name":"microRNA 6740 [Source:HGNC Symbol;Acc:HGNC:50082]","synonyms":"hsa-mir-6740","biotype":"miRNA","ncbi_id":"102465443","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":202003124,"end":202003236,"strand":1,"description":"microRNA 6740 [Source:HGNC Symbol;Acc:HGNC:50082]"}, {"versioned_ensembl_gene_id":"ENSG00000200107.1","gene_symbol":"RNU6-1249P","gene_name":"RNA, U6 small nuclear 1249, pseudogene [Source:HGNC Symbol;Acc:HGNC:48212]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480652","summary":null,"start":55551810,"end":55551920,"strand":1,"description":"RNA, U6 small nuclear 1249, pseudogene [Source:HGNC Symbol;Acc:HGNC:48212]"}, {"versioned_ensembl_gene_id":"ENSG00000201302.1","gene_symbol":"SNORA65","gene_name":"small nucleolar RNA, H/ACA box 65 [Source:HGNC Symbol;Acc:HGNC:10222]","synonyms":"U65,RNU65","biotype":"snoRNA","ncbi_id":"26783","summary":null,"start":127448501,"end":127448630,"strand":-1,"description":"small nucleolar RNA, H/ACA box 65 [Source:HGNC Symbol;Acc:HGNC:10222]"}, {"versioned_ensembl_gene_id":"ENSG00000265777.2","gene_symbol":"RN7SL624P","gene_name":"RNA, 7SL, cytoplasmic 624, pseudogene [Source:HGNC Symbol;Acc:HGNC:46640]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480379","summary":null,"start":2199762,"end":2200039,"strand":1,"description":"RNA, 7SL, cytoplasmic 624, pseudogene [Source:HGNC Symbol;Acc:HGNC:46640]"}, {"versioned_ensembl_gene_id":"ENSG00000238658.1","gene_symbol":"RNU6-625P","gene_name":"RNA, U6 small nuclear 625, pseudogene [Source:HGNC Symbol;Acc:HGNC:47588]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479843","summary":null,"start":78066947,"end":78067053,"strand":1,"description":"RNA, U6 small nuclear 625, pseudogene [Source:HGNC Symbol;Acc:HGNC:47588]"}, {"versioned_ensembl_gene_id":"ENSG00000207922.1","gene_symbol":"MIR566","gene_name":"microRNA 566 [Source:HGNC Symbol;Acc:HGNC:32822]","synonyms":"MIRN566,hsa-mir-566","biotype":"miRNA","ncbi_id":"693151","summary":"This record was withdrawn by miRBase.","start":50173326,"end":50173419,"strand":1,"description":"microRNA 566 [Source:HGNC Symbol;Acc:HGNC:32822]"}, {"versioned_ensembl_gene_id":"ENSG00000207275.1","gene_symbol":"RNU6-441P","gene_name":"RNA, U6 small nuclear 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:47404]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480392","summary":null,"start":82340771,"end":82340876,"strand":1,"description":"RNA, U6 small nuclear 441, pseudogene [Source:HGNC Symbol;Acc:HGNC:47404]"}, {"versioned_ensembl_gene_id":"ENSG00000278465.1","gene_symbol":"MIR6769B","gene_name":"microRNA 6769b [Source:HGNC Symbol;Acc:HGNC:50016]","synonyms":"hsa-mir-6769b","biotype":"miRNA","ncbi_id":"102466202","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":206474803,"end":206474864,"strand":1,"description":"microRNA 6769b [Source:HGNC Symbol;Acc:HGNC:50016]"}, {"versioned_ensembl_gene_id":"ENSG00000278520.1","gene_symbol":"MIR7851","gene_name":"microRNA 7851 [Source:HGNC Symbol;Acc:HGNC:50127]","synonyms":"hsa-mir-7851","biotype":"miRNA","ncbi_id":"102467003","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42323700,"end":42323859,"strand":-1,"description":"microRNA 7851 [Source:HGNC Symbol;Acc:HGNC:50127]"}, {"versioned_ensembl_gene_id":"ENSG00000206805.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":48479097,"end":48479198,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000200437.1","gene_symbol":"RNU6-799P","gene_name":"RNA, U6 small nuclear 799, pseudogene [Source:HGNC Symbol;Acc:HGNC:47762]","synonyms":null,"biotype":"snRNA","ncbi_id":"107105254","summary":null,"start":15311345,"end":15311451,"strand":1,"description":"RNA, U6 small nuclear 799, pseudogene [Source:HGNC Symbol;Acc:HGNC:47762]"}, {"versioned_ensembl_gene_id":"ENSG00000207993.3","gene_symbol":"MIR134","gene_name":"microRNA 134 [Source:HGNC Symbol;Acc:HGNC:31519]","synonyms":"MIRN134,hsa-mir-134","biotype":"miRNA","ncbi_id":"406924","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":101054687,"end":101054759,"strand":1,"description":"microRNA 134 [Source:HGNC Symbol;Acc:HGNC:31519]"}, {"versioned_ensembl_gene_id":"ENSG00000274059.1","gene_symbol":"5S_rRNA","gene_name":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]","synonyms":null,"biotype":"rRNA","ncbi_id":null,"summary":null,"start":207708898,"end":207708981,"strand":-1,"description":"5S ribosomal RNA [Source:RFAM;Acc:RF00001]"}, {"versioned_ensembl_gene_id":"ENSG00000265005.1","gene_symbol":"MIR548W","gene_name":"microRNA 548w [Source:HGNC Symbol;Acc:HGNC:38255]","synonyms":"hsa-mir-548w","biotype":"miRNA","ncbi_id":"100422923","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26025237,"end":26025310,"strand":1,"description":"microRNA 548w [Source:HGNC Symbol;Acc:HGNC:38255]"}, {"versioned_ensembl_gene_id":"ENSG00000207948.3","gene_symbol":"MIR328","gene_name":"microRNA 328 [Source:HGNC Symbol;Acc:HGNC:31770]","synonyms":"MIRN328,hsa-mir-328","biotype":"miRNA","ncbi_id":"442901","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":67202321,"end":67202395,"strand":-1,"description":"microRNA 328 [Source:HGNC Symbol;Acc:HGNC:31770]"}, {"versioned_ensembl_gene_id":"ENSG00000238427.1","gene_symbol":"RNU7-136P","gene_name":"RNA, U7 small nuclear 136 pseudogene [Source:HGNC Symbol;Acc:HGNC:45670]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479076","summary":null,"start":160472348,"end":160472416,"strand":-1,"description":"RNA, U7 small nuclear 136 pseudogene [Source:HGNC Symbol;Acc:HGNC:45670]"}, {"versioned_ensembl_gene_id":"ENSG00000201324.1","gene_symbol":"RNU6-361P","gene_name":"RNA, U6 small nuclear 361, pseudogene [Source:HGNC Symbol;Acc:HGNC:47324]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480574","summary":null,"start":108926435,"end":108926541,"strand":-1,"description":"RNA, U6 small nuclear 361, pseudogene [Source:HGNC Symbol;Acc:HGNC:47324]"}, {"versioned_ensembl_gene_id":"ENSG00000277968.1","gene_symbol":"SPRY4-IT1_1","gene_name":"SPRY4-IT1 conserved region 1 [Source:RFAM;Acc:RF02038]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":142317830,"end":142317920,"strand":1,"description":"SPRY4-IT1 conserved region 1 [Source:RFAM;Acc:RF02038]"}, {"versioned_ensembl_gene_id":"ENSG00000278853.1","gene_symbol":"RNU6-55P","gene_name":"RNA, U6 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:42545]","synonyms":"RNU6-55","biotype":"snRNA","ncbi_id":"100873763","summary":null,"start":18869185,"end":18869291,"strand":-1,"description":"RNA, U6 small nuclear 55, pseudogene [Source:HGNC Symbol;Acc:HGNC:42545]"}, {"versioned_ensembl_gene_id":"ENSG00000206913.1","gene_symbol":"SNORA7","gene_name":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":74252414,"end":74252552,"strand":-1,"description":"Small nucleolar RNA SNORA7 [Source:RFAM;Acc:RF00409]"}, {"versioned_ensembl_gene_id":"ENSG00000263942.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30123209,"end":30123371,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000201727.1","gene_symbol":"RNA5SP173","gene_name":"RNA, 5S ribosomal pseudogene 173 [Source:HGNC Symbol;Acc:HGNC:43073]","synonyms":"RN5S173","biotype":"rRNA","ncbi_id":"100873437","summary":null,"start":178406695,"end":178406830,"strand":1,"description":"RNA, 5S ribosomal pseudogene 173 [Source:HGNC Symbol;Acc:HGNC:43073]"}, {"versioned_ensembl_gene_id":"ENSG00000274111.1","gene_symbol":"MIR6777","gene_name":"microRNA 6777 [Source:HGNC Symbol;Acc:HGNC:50173]","synonyms":"hsa-mir-6777","biotype":"miRNA","ncbi_id":"102465466","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":17813480,"end":17813545,"strand":-1,"description":"microRNA 6777 [Source:HGNC Symbol;Acc:HGNC:50173]"}, {"versioned_ensembl_gene_id":"ENSG00000207237.1","gene_symbol":"RNU6-110P","gene_name":"RNA, U6 small nuclear 110, pseudogene [Source:HGNC Symbol;Acc:HGNC:47073]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479615","summary":null,"start":25964197,"end":25964300,"strand":1,"description":"RNA, U6 small nuclear 110, pseudogene [Source:HGNC Symbol;Acc:HGNC:47073]"}, {"versioned_ensembl_gene_id":"ENSG00000283394.1","gene_symbol":"MIR7515","gene_name":"microRNA 7515 [Source:HGNC Symbol;Acc:HGNC:49839]","synonyms":"hsa-mir-7515","biotype":"miRNA","ncbi_id":"102466235","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":6650373,"end":6650439,"strand":1,"description":"microRNA 7515 [Source:HGNC Symbol;Acc:HGNC:49839]"}, {"versioned_ensembl_gene_id":"ENSG00000222246.1","gene_symbol":"MIR1471","gene_name":"microRNA 1471 [Source:HGNC Symbol;Acc:HGNC:35380]","synonyms":"MIRN1471,hsa-mir-1471","biotype":"miRNA","ncbi_id":"100302126","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":231892242,"end":231892298,"strand":-1,"description":"microRNA 1471 [Source:HGNC Symbol;Acc:HGNC:35380]"}, {"versioned_ensembl_gene_id":"ENSG00000222649.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":119057880,"end":119057974,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000243426.3","gene_symbol":"RN7SL454P","gene_name":"RNA, 7SL, cytoplasmic 454, pseudogene [Source:HGNC Symbol;Acc:HGNC:46470]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479388","summary":null,"start":78532813,"end":78533055,"strand":-1,"description":"RNA, 7SL, cytoplasmic 454, pseudogene [Source:HGNC Symbol;Acc:HGNC:46470]"}, {"versioned_ensembl_gene_id":"ENSG00000207638.1","gene_symbol":"MIR99A","gene_name":"microRNA 99a [Source:HGNC Symbol;Acc:HGNC:31650]","synonyms":"hsa-mir-99a,MIRN99A","biotype":"miRNA","ncbi_id":"407055","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16539089,"end":16539169,"strand":1,"description":"microRNA 99a [Source:HGNC Symbol;Acc:HGNC:31650]"}, {"versioned_ensembl_gene_id":"ENSG00000278433.1","gene_symbol":"MIR6070","gene_name":"microRNA 6070 [Source:HGNC Symbol;Acc:HGNC:49950]","synonyms":"hsa-mir-6070","biotype":"miRNA","ncbi_id":"102464825","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":43609887,"end":43609989,"strand":-1,"description":"microRNA 6070 [Source:HGNC Symbol;Acc:HGNC:49950]"}, {"versioned_ensembl_gene_id":"ENSG00000251967.1","gene_symbol":"SNORD77","gene_name":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]","synonyms":null,"biotype":"snoRNA","ncbi_id":"692197","summary":null,"start":46650510,"end":46650590,"strand":1,"description":"Small nucleolar RNA SNORD77 [Source:RFAM;Acc:RF00591]"}, {"versioned_ensembl_gene_id":"ENSG00000284464.1","gene_symbol":"MIR1306","gene_name":"microRNA 1306 [Source:HGNC Symbol;Acc:HGNC:35371]","synonyms":"MIRN1306,hsa-mir-1306","biotype":"miRNA","ncbi_id":"100302197","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":20086058,"end":20086142,"strand":1,"description":"microRNA 1306 [Source:HGNC Symbol;Acc:HGNC:35371]"}, {"versioned_ensembl_gene_id":"ENSG00000207689.1","gene_symbol":"MIR548A2","gene_name":"microRNA 548a-2 [Source:HGNC Symbol;Acc:HGNC:32797]","synonyms":"MIRN548A2,hsa-mir-548a-2","biotype":"miRNA","ncbi_id":"693126","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":135239160,"end":135239256,"strand":1,"description":"microRNA 548a-2 [Source:HGNC Symbol;Acc:HGNC:32797]"}, {"versioned_ensembl_gene_id":"ENSG00000199349.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206747980,"end":206748092,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199158.1","gene_symbol":"MIR96","gene_name":"microRNA 96 [Source:HGNC Symbol;Acc:HGNC:31648]","synonyms":"MIRN96,hsa-mir-96,DFNA50","biotype":"miRNA","ncbi_id":"407053","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129774692,"end":129774769,"strand":-1,"description":"microRNA 96 [Source:HGNC Symbol;Acc:HGNC:31648]"}, {"versioned_ensembl_gene_id":"ENSG00000264495.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":29747442,"end":29747543,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000242699.3","gene_symbol":"RN7SL516P","gene_name":"RNA, 7SL, cytoplasmic 516, pseudogene [Source:HGNC Symbol;Acc:HGNC:46532]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479411","summary":null,"start":29681027,"end":29681323,"strand":-1,"description":"RNA, 7SL, cytoplasmic 516, pseudogene [Source:HGNC Symbol;Acc:HGNC:46532]"}, {"versioned_ensembl_gene_id":"ENSG00000263372.1","gene_symbol":"MIR548AO","gene_name":"microRNA 548ao [Source:HGNC Symbol;Acc:HGNC:43539]","synonyms":"hsa-mir-548ao","biotype":"miRNA","ncbi_id":"100847068","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41271048,"end":41271143,"strand":-1,"description":"microRNA 548ao [Source:HGNC Symbol;Acc:HGNC:43539]"}, {"versioned_ensembl_gene_id":"ENSG00000283505.1","gene_symbol":"MIR5681B","gene_name":"microRNA 5681b [Source:HGNC Symbol;Acc:HGNC:43538]","synonyms":"hsa-mir-5681b","biotype":"miRNA","ncbi_id":"100847091","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74548550,"end":74548609,"strand":-1,"description":"microRNA 5681b [Source:HGNC Symbol;Acc:HGNC:43538]"}, {"versioned_ensembl_gene_id":"ENSG00000251992.1","gene_symbol":"SCARNA17","gene_name":"small Cajal body-specific RNA 17 [Source:HGNC Symbol;Acc:HGNC:32574]","synonyms":"U91,mgU12-22/U4-8","biotype":"scaRNA","ncbi_id":"677769","summary":null,"start":49814133,"end":49814276,"strand":1,"description":"small Cajal body-specific RNA 17 [Source:HGNC Symbol;Acc:HGNC:32574]"}, {"versioned_ensembl_gene_id":"ENSG00000284087.1","gene_symbol":"MIR6844","gene_name":"microRNA 6844 [Source:HGNC Symbol;Acc:HGNC:50135]","synonyms":"hsa-mir-6844","biotype":"miRNA","ncbi_id":"102466200","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":124508515,"end":124508576,"strand":-1,"description":"microRNA 6844 [Source:HGNC Symbol;Acc:HGNC:50135]"}, {"versioned_ensembl_gene_id":"ENSG00000201432.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36337667,"end":36337778,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283146.1","gene_symbol":"MIR548AU","gene_name":"microRNA 548au [Source:HGNC Symbol;Acc:HGNC:43483]","synonyms":"hsa-mir-548au","biotype":"miRNA","ncbi_id":"100847045","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93594841,"end":93594894,"strand":1,"description":"microRNA 548au [Source:HGNC Symbol;Acc:HGNC:43483]"}, {"versioned_ensembl_gene_id":"ENSG00000207969.1","gene_symbol":"MIR507","gene_name":"microRNA 507 [Source:HGNC Symbol;Acc:HGNC:32144]","synonyms":"MIRN507,hsa-mir-507","biotype":"miRNA","ncbi_id":"574512","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147230984,"end":147231077,"strand":-1,"description":"microRNA 507 [Source:HGNC Symbol;Acc:HGNC:32144]"}, {"versioned_ensembl_gene_id":"ENSG00000199470.1","gene_symbol":"SNORA64","gene_name":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]","synonyms":"U64,RNU64","biotype":"snoRNA","ncbi_id":"26784","summary":null,"start":12700758,"end":12700889,"strand":-1,"description":"Small nucleolar RNA SNORA64/SNORA10 family [Source:RFAM;Acc:RF00264]"}, {"versioned_ensembl_gene_id":"ENSG00000223203.1","gene_symbol":"RNA5SP221","gene_name":"RNA, 5S ribosomal pseudogene 221 [Source:HGNC Symbol;Acc:HGNC:43121]","synonyms":"RN5S221","biotype":"rRNA","ncbi_id":"106480759","summary":null,"start":143449809,"end":143449911,"strand":1,"description":"RNA, 5S ribosomal pseudogene 221 [Source:HGNC Symbol;Acc:HGNC:43121]"}, {"versioned_ensembl_gene_id":"ENSG00000212567.1","gene_symbol":"SNORA57","gene_name":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]","synonyms":"U99","biotype":"snoRNA","ncbi_id":"692158","summary":null,"start":40790077,"end":40790204,"strand":-1,"description":"Small nucleolar RNA SNORA57 [Source:RFAM;Acc:RF00191]"}, {"versioned_ensembl_gene_id":"ENSG00000201885.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":77013583,"end":77013684,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252718.1","gene_symbol":"RNU6-612P","gene_name":"RNA, U6 small nuclear 612, pseudogene [Source:HGNC Symbol;Acc:HGNC:47575]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481374","summary":null,"start":60719640,"end":60719741,"strand":1,"description":"RNA, U6 small nuclear 612, pseudogene [Source:HGNC Symbol;Acc:HGNC:47575]"}, {"versioned_ensembl_gene_id":"ENSG00000252151.1","gene_symbol":"RNU6-1265P","gene_name":"RNA, U6 small nuclear 1265, pseudogene [Source:HGNC Symbol;Acc:HGNC:48228]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481579","summary":null,"start":14124233,"end":14124335,"strand":-1,"description":"RNA, U6 small nuclear 1265, pseudogene [Source:HGNC Symbol;Acc:HGNC:48228]"}, {"versioned_ensembl_gene_id":"ENSG00000276670.1","gene_symbol":"Six3os1_7","gene_name":"Six3os1 conserved region 7 [Source:RFAM;Acc:RF02252]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":44940045,"end":44940245,"strand":1,"description":"Six3os1 conserved region 7 [Source:RFAM;Acc:RF02252]"}, {"versioned_ensembl_gene_id":"ENSG00000273730.1","gene_symbol":"RNA5-8SN3","gene_name":"RNA, 5.8S ribosomal N3 [Source:HGNC Symbol;Acc:HGNC:53525]","synonyms":null,"biotype":"rRNA","ncbi_id":"109910381","summary":"45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through RNR5, respectively. Each cluster consists of multiple 45S rDNA repeat units that vary in number among individuals and chromosomes, with total diploid copy number estimates ranging from 60 to >800 repeat units in a human genome. The 45S rDNA repeat unit encodes a 45S rRNA precursor, transcribed by RNA polymerase I, which is processed to form the 18S, 5.8S and 28S rRNAs. This gene represents a copy of the 5.8S ribosomal RNA on chromosome 21. [provided by RefSeq, Mar 2017]","start":155997,"end":156149,"strand":1,"description":"RNA, 5.8S ribosomal N3 [Source:HGNC Symbol;Acc:HGNC:53525]"}, {"versioned_ensembl_gene_id":"ENSG00000242719.3","gene_symbol":"RN7SL806P","gene_name":"RNA, 7SL, cytoplasmic 806, pseudogene [Source:HGNC Symbol;Acc:HGNC:46822]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479515","summary":null,"start":42881236,"end":42881517,"strand":1,"description":"RNA, 7SL, cytoplasmic 806, pseudogene [Source:HGNC Symbol;Acc:HGNC:46822]"}, {"versioned_ensembl_gene_id":"ENSG00000252130.1","gene_symbol":"RNU6-1045P","gene_name":"RNA, U6 small nuclear 1045, pseudogene [Source:HGNC Symbol;Acc:HGNC:48008]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480025","summary":null,"start":191370938,"end":191371044,"strand":1,"description":"RNA, U6 small nuclear 1045, pseudogene [Source:HGNC Symbol;Acc:HGNC:48008]"}, {"versioned_ensembl_gene_id":"ENSG00000252462.1","gene_symbol":"RNU6-113P","gene_name":"RNA, U6 small nuclear 113, pseudogene [Source:HGNC Symbol;Acc:HGNC:47076]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479616","summary":null,"start":17431547,"end":17431647,"strand":1,"description":"RNA, U6 small nuclear 113, pseudogene [Source:HGNC Symbol;Acc:HGNC:47076]"}, {"versioned_ensembl_gene_id":"ENSG00000252325.1","gene_symbol":"RNU6-1038P","gene_name":"RNA, U6 small nuclear 1038, pseudogene [Source:HGNC Symbol;Acc:HGNC:48001]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480022","summary":null,"start":21879801,"end":21879904,"strand":1,"description":"RNA, U6 small nuclear 1038, pseudogene [Source:HGNC Symbol;Acc:HGNC:48001]"}, {"versioned_ensembl_gene_id":"ENSG00000238833.1","gene_symbol":"RNU1-131P","gene_name":"RNA, U1 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:48473]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480193","summary":null,"start":17209060,"end":17209220,"strand":1,"description":"RNA, U1 small nuclear 131, pseudogene [Source:HGNC Symbol;Acc:HGNC:48473]"}, {"versioned_ensembl_gene_id":"ENSG00000274199.1","gene_symbol":"DLEU2_1","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 1 [Source:RFAM;Acc:RF02105]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":63549489,"end":63549608,"strand":-1,"description":"Deleted in lymphocytic leukemia 2 conserved region 1 [Source:RFAM;Acc:RF02105]"}, {"versioned_ensembl_gene_id":"ENSG00000206665.1","gene_symbol":"RNU6-573P","gene_name":"RNA, U6 small nuclear 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:47536]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480591","summary":null,"start":35495898,"end":35496003,"strand":1,"description":"RNA, U6 small nuclear 573, pseudogene [Source:HGNC Symbol;Acc:HGNC:47536]"}, {"versioned_ensembl_gene_id":"ENSG00000272197.2","gene_symbol":"RN7SL803P","gene_name":"RNA, 7SL, cytoplasmic 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:46819]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479514","summary":null,"start":154718383,"end":154718689,"strand":-1,"description":"RNA, 7SL, cytoplasmic 803, pseudogene [Source:HGNC Symbol;Acc:HGNC:46819]"}, {"versioned_ensembl_gene_id":"ENSG00000199900.1","gene_symbol":"RNA5SP463","gene_name":"RNA, 5S ribosomal pseudogene 463 [Source:HGNC Symbol;Acc:HGNC:43363]","synonyms":"RN5S463","biotype":"rRNA","ncbi_id":"100873707","summary":null,"start":7886977,"end":7887096,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 463 [Source:HGNC Symbol;Acc:HGNC:43363]"}, {"versioned_ensembl_gene_id":"ENSG00000199646.1","gene_symbol":"RNU6-1272P","gene_name":"RNA, U6 small nuclear 1272, pseudogene [Source:HGNC Symbol;Acc:HGNC:48235]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480121","summary":null,"start":138876359,"end":138876465,"strand":-1,"description":"RNA, U6 small nuclear 1272, pseudogene [Source:HGNC Symbol;Acc:HGNC:48235]"}, {"versioned_ensembl_gene_id":"ENSG00000275631.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":9646825,"end":9647000,"strand":1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000251986.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41868998,"end":41869095,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252481.1","gene_symbol":"SCARNA13","gene_name":"small Cajal body-specific RNA 13 [Source:HGNC Symbol;Acc:HGNC:32570]","synonyms":"U93","biotype":"scaRNA","ncbi_id":"677768","summary":null,"start":95533355,"end":95533629,"strand":-1,"description":"small Cajal body-specific RNA 13 [Source:HGNC Symbol;Acc:HGNC:32570]"}, {"versioned_ensembl_gene_id":"ENSG00000252022.1","gene_symbol":"SNORD33","gene_name":"Small nucleolar RNA Z195/SNORD33/SNORD32 family [Source:RFAM;Acc:RF00133]","synonyms":"U33,RNU33","biotype":"snoRNA","ncbi_id":"26818","summary":null,"start":76469508,"end":76469595,"strand":-1,"description":"Small nucleolar RNA Z195/SNORD33/SNORD32 family [Source:RFAM;Acc:RF00133]"}, {"versioned_ensembl_gene_id":"ENSG00000202276.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":8877417,"end":8877518,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000223280.1","gene_symbol":"RNU6-57P","gene_name":"RNA, U6 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:42547]","synonyms":"RNU6-57","biotype":"snRNA","ncbi_id":"100873765","summary":null,"start":41354557,"end":41354659,"strand":-1,"description":"RNA, U6 small nuclear 57, pseudogene [Source:HGNC Symbol;Acc:HGNC:42547]"}, {"versioned_ensembl_gene_id":"ENSG00000222704.1","gene_symbol":"RN7SKP182","gene_name":"RNA, 7SK small nuclear pseudogene 182 [Source:HGNC Symbol;Acc:HGNC:45906]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479177","summary":null,"start":39016047,"end":39016344,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 182 [Source:HGNC Symbol;Acc:HGNC:45906]"}, {"versioned_ensembl_gene_id":"ENSG00000212410.1","gene_symbol":"RNU6-932P","gene_name":"RNA, U6 small nuclear 932, pseudogene [Source:HGNC Symbol;Acc:HGNC:47895]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481474","summary":null,"start":157985789,"end":157985894,"strand":-1,"description":"RNA, U6 small nuclear 932, pseudogene [Source:HGNC Symbol;Acc:HGNC:47895]"}, {"versioned_ensembl_gene_id":"ENSG00000200247.1","gene_symbol":"RNU6-254P","gene_name":"RNA, U6 small nuclear 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:47217]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479679","summary":null,"start":19445949,"end":19446055,"strand":-1,"description":"RNA, U6 small nuclear 254, pseudogene [Source:HGNC Symbol;Acc:HGNC:47217]"}, {"versioned_ensembl_gene_id":"ENSG00000206824.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50386145,"end":50386246,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266580.1","gene_symbol":"MIR4254","gene_name":"microRNA 4254 [Source:HGNC Symbol;Acc:HGNC:38193]","synonyms":"hsa-mir-4254","biotype":"miRNA","ncbi_id":"100423028","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":31758660,"end":31758735,"strand":-1,"description":"microRNA 4254 [Source:HGNC Symbol;Acc:HGNC:38193]"}, {"versioned_ensembl_gene_id":"ENSG00000273525.1","gene_symbol":"SNORA54","gene_name":"small nucleolar RNA, H/ACA box 54 [Source:HGNC Symbol;Acc:HGNC:32647]","synonyms":"ACA54,ACA54","biotype":"snoRNA","ncbi_id":"677833","summary":null,"start":2962636,"end":2962758,"strand":-1,"description":"small nucleolar RNA, H/ACA box 54 [Source:HGNC Symbol;Acc:HGNC:32647]"}, {"versioned_ensembl_gene_id":"ENSG00000199932.1","gene_symbol":"RNU1-18P","gene_name":"RNA, U1 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:41944]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873815","summary":null,"start":122211648,"end":122211811,"strand":1,"description":"RNA, U1 small nuclear 18, pseudogene [Source:HGNC Symbol;Acc:HGNC:41944]"}, {"versioned_ensembl_gene_id":"ENSG00000263795.1","gene_symbol":"MIR5100","gene_name":"microRNA 5100 [Source:HGNC Symbol;Acc:HGNC:43540]","synonyms":"hsa-mir-5100","biotype":"miRNA","ncbi_id":"100847014","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":42997563,"end":42997681,"strand":1,"description":"microRNA 5100 [Source:HGNC Symbol;Acc:HGNC:43540]"}, {"versioned_ensembl_gene_id":"ENSG00000201524.1","gene_symbol":"RNU6-450P","gene_name":"RNA, U6 small nuclear 450, pseudogene [Source:HGNC Symbol;Acc:HGNC:47413]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481321","summary":null,"start":59847438,"end":59847544,"strand":-1,"description":"RNA, U6 small nuclear 450, pseudogene [Source:HGNC Symbol;Acc:HGNC:47413]"}, {"versioned_ensembl_gene_id":"ENSG00000273612.1","gene_symbol":"DLEU2_4","gene_name":"Deleted in lymphocytic leukemia 2 conserved region 4 [Source:RFAM;Acc:RF02108]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50068107,"end":50068164,"strand":1,"description":"Deleted in lymphocytic leukemia 2 conserved region 4 [Source:RFAM;Acc:RF02108]"}, {"versioned_ensembl_gene_id":"ENSG00000283476.1","gene_symbol":"MIR1279","gene_name":"microRNA 1279 [Source:HGNC Symbol;Acc:HGNC:35357]","synonyms":"MIRN1279,hsa-mir-1279","biotype":"miRNA","ncbi_id":"100302182","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69273157,"end":69273218,"strand":-1,"description":"microRNA 1279 [Source:HGNC Symbol;Acc:HGNC:35357]"}, {"versioned_ensembl_gene_id":"ENSG00000199638.1","gene_symbol":"RNA5SP319","gene_name":"RNA, 5S ribosomal pseudogene 319 [Source:HGNC Symbol;Acc:HGNC:43219]","synonyms":"RN5S319","biotype":"rRNA","ncbi_id":"100873585","summary":null,"start":68461407,"end":68461525,"strand":1,"description":"RNA, 5S ribosomal pseudogene 319 [Source:HGNC Symbol;Acc:HGNC:43219]"}, {"versioned_ensembl_gene_id":"ENSG00000252172.1","gene_symbol":"RNU6-720P","gene_name":"RNA, U6 small nuclear 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:47683]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479885","summary":null,"start":149917342,"end":149917449,"strand":-1,"description":"RNA, U6 small nuclear 720, pseudogene [Source:HGNC Symbol;Acc:HGNC:47683]"}, {"versioned_ensembl_gene_id":"ENSG00000278708.1","gene_symbol":"HOTTIP_2","gene_name":"HOXA transcript at the distal tip, conserved region 2 [Source:RFAM;Acc:RF02041]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27201844,"end":27202219,"strand":1,"description":"HOXA transcript at the distal tip, conserved region 2 [Source:RFAM;Acc:RF02041]"}, {"versioned_ensembl_gene_id":"ENSG00000276765.1","gene_symbol":"MIR8073","gene_name":"microRNA 8073 [Source:HGNC Symbol;Acc:HGNC:50131]","synonyms":"hsa-mir-8073","biotype":"miRNA","ncbi_id":"102465872","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":110340958,"end":110341029,"strand":1,"description":"microRNA 8073 [Source:HGNC Symbol;Acc:HGNC:50131]"}, {"versioned_ensembl_gene_id":"ENSG00000252446.1","gene_symbol":"RNU6-405P","gene_name":"RNA, U6 small nuclear 405, pseudogene [Source:HGNC Symbol;Acc:HGNC:47368]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479744","summary":null,"start":16691798,"end":16691907,"strand":1,"description":"RNA, U6 small nuclear 405, pseudogene [Source:HGNC Symbol;Acc:HGNC:47368]"}, {"versioned_ensembl_gene_id":"ENSG00000241939.3","gene_symbol":"RN7SL517P","gene_name":"RNA, 7SL, cytoplasmic 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:46533]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481064","summary":null,"start":43314951,"end":43315255,"strand":1,"description":"RNA, 7SL, cytoplasmic 517, pseudogene [Source:HGNC Symbol;Acc:HGNC:46533]"}, {"versioned_ensembl_gene_id":"ENSG00000241188.3","gene_symbol":"RN7SL165P","gene_name":"RNA, 7SL, cytoplasmic 165, pseudogene [Source:HGNC Symbol;Acc:HGNC:46181]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479281","summary":null,"start":26814822,"end":26815112,"strand":1,"description":"RNA, 7SL, cytoplasmic 165, pseudogene [Source:HGNC Symbol;Acc:HGNC:46181]"}, {"versioned_ensembl_gene_id":"ENSG00000251937.1","gene_symbol":"RNU7-129P","gene_name":"RNA, U7 small nuclear 129 pseudogene [Source:HGNC Symbol;Acc:HGNC:45663]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480450","summary":null,"start":12400412,"end":12400473,"strand":1,"description":"RNA, U7 small nuclear 129 pseudogene [Source:HGNC Symbol;Acc:HGNC:45663]"}, {"versioned_ensembl_gene_id":"ENSG00000274980.1","gene_symbol":"RNU6-1025P","gene_name":"RNA, U6 small nuclear 1025, pseudogene [Source:HGNC Symbol;Acc:HGNC:47988]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480018","summary":null,"start":948421,"end":948524,"strand":1,"description":"RNA, U6 small nuclear 1025, pseudogene [Source:HGNC Symbol;Acc:HGNC:47988]"}, {"versioned_ensembl_gene_id":"ENSG00000251898.1","gene_symbol":"SCARNA11","gene_name":"small Cajal body-specific RNA 11 [Source:HGNC Symbol;Acc:HGNC:32568]","synonyms":"ACA57","biotype":"scaRNA","ncbi_id":"677780","summary":null,"start":6581474,"end":6581609,"strand":-1,"description":"small Cajal body-specific RNA 11 [Source:HGNC Symbol;Acc:HGNC:32568]"}, {"versioned_ensembl_gene_id":"ENSG00000264406.1","gene_symbol":"MIR548AP","gene_name":"microRNA 548ap [Source:HGNC Symbol;Acc:HGNC:43465]","synonyms":"hsa-mir-548ap","biotype":"miRNA","ncbi_id":"100847084","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":85825635,"end":85825730,"strand":1,"description":"microRNA 548ap [Source:HGNC Symbol;Acc:HGNC:43465]"}, {"versioned_ensembl_gene_id":"ENSG00000251813.1","gene_symbol":"RNU6-983P","gene_name":"RNA, U6 small nuclear 983, pseudogene [Source:HGNC Symbol;Acc:HGNC:47946]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481490","summary":null,"start":194488103,"end":194488205,"strand":-1,"description":"RNA, U6 small nuclear 983, pseudogene [Source:HGNC Symbol;Acc:HGNC:47946]"}, {"versioned_ensembl_gene_id":"ENSG00000265509.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31487449,"end":31487550,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000266235.1","gene_symbol":"MIR3176","gene_name":"microRNA 3176 [Source:HGNC Symbol;Acc:HGNC:38345]","synonyms":"hsa-mir-3176","biotype":"miRNA","ncbi_id":"100423037","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":543277,"end":543366,"strand":1,"description":"microRNA 3176 [Source:HGNC Symbol;Acc:HGNC:38345]"}, {"versioned_ensembl_gene_id":"ENSG00000200295.1","gene_symbol":"RNU6-527P","gene_name":"RNA, U6 small nuclear 527, pseudogene [Source:HGNC Symbol;Acc:HGNC:47490]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480587","summary":null,"start":106607716,"end":106607819,"strand":1,"description":"RNA, U6 small nuclear 527, pseudogene [Source:HGNC Symbol;Acc:HGNC:47490]"}, {"versioned_ensembl_gene_id":"ENSG00000276932.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":93050,"end":93150,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284473.1","gene_symbol":"MIR4720","gene_name":"microRNA 4720 [Source:HGNC Symbol;Acc:HGNC:41705]","synonyms":"hsa-mir-4720","biotype":"miRNA","ncbi_id":"100616150","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":81385018,"end":81385093,"strand":1,"description":"microRNA 4720 [Source:HGNC Symbol;Acc:HGNC:41705]"}, {"versioned_ensembl_gene_id":"ENSG00000264484.2","gene_symbol":"RN7SL697P","gene_name":"RNA, 7SL, cytoplasmic 697, pseudogene [Source:HGNC Symbol;Acc:HGNC:46713]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480526","summary":null,"start":154495815,"end":154496113,"strand":-1,"description":"RNA, 7SL, cytoplasmic 697, pseudogene [Source:HGNC Symbol;Acc:HGNC:46713]"}, {"versioned_ensembl_gene_id":"ENSG00000263589.1","gene_symbol":"SNORA48","gene_name":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]","synonyms":"SNORA48A,ACA48","biotype":"snoRNA","ncbi_id":"652965","summary":null,"start":30177929,"end":30178090,"strand":-1,"description":"Small nucleolar RNA SNORA48 [Source:RFAM;Acc:RF00554]"}, {"versioned_ensembl_gene_id":"ENSG00000200139.1","gene_symbol":"RNU6-778P","gene_name":"RNA, U6 small nuclear 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:47741]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479910","summary":null,"start":199888159,"end":199888261,"strand":1,"description":"RNA, U6 small nuclear 778, pseudogene [Source:HGNC Symbol;Acc:HGNC:47741]"}, {"versioned_ensembl_gene_id":"ENSG00000283796.1","gene_symbol":"MIR6510","gene_name":"microRNA 6510 [Source:HGNC Symbol;Acc:HGNC:50101]","synonyms":"hsa-mir-6510","biotype":"miRNA","ncbi_id":"102466658","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41517164,"end":41517217,"strand":-1,"description":"microRNA 6510 [Source:HGNC Symbol;Acc:HGNC:50101]"}, {"versioned_ensembl_gene_id":"ENSG00000199867.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62330812,"end":62330913,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000275942.1","gene_symbol":"MIAT_exon5_2","gene_name":"Myocardial infarction associated transcript exon 5 conserved region 2 [Source:RFAM;Acc:RF01876]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":26672164,"end":26672248,"strand":1,"description":"Myocardial infarction associated transcript exon 5 conserved region 2 [Source:RFAM;Acc:RF01876]"}, {"versioned_ensembl_gene_id":"ENSG00000202016.1","gene_symbol":"RNU6-619P","gene_name":"RNA, U6 small nuclear 619, pseudogene [Source:HGNC Symbol;Acc:HGNC:47582]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479840","summary":null,"start":222498291,"end":222498398,"strand":1,"description":"RNA, U6 small nuclear 619, pseudogene [Source:HGNC Symbol;Acc:HGNC:47582]"}, {"versioned_ensembl_gene_id":"ENSG00000267959.3","gene_symbol":"MIR3188","gene_name":"microRNA 3188 [Source:HGNC Symbol;Acc:HGNC:38226]","synonyms":"hsa-mir-3188","biotype":"miRNA","ncbi_id":"100422833","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18282077,"end":18282161,"strand":1,"description":"microRNA 3188 [Source:HGNC Symbol;Acc:HGNC:38226]"}, {"versioned_ensembl_gene_id":"ENSG00000264703.1","gene_symbol":"MIR4752","gene_name":"microRNA 4752 [Source:HGNC Symbol;Acc:HGNC:41803]","synonyms":"hsa-mir-4752","biotype":"miRNA","ncbi_id":"100616171","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":54282109,"end":54282180,"strand":1,"description":"microRNA 4752 [Source:HGNC Symbol;Acc:HGNC:41803]"}, {"versioned_ensembl_gene_id":"ENSG00000201555.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":31778817,"end":31778905,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212290.1","gene_symbol":"RNA5SP424","gene_name":"RNA, 5S ribosomal pseudogene 424 [Source:HGNC Symbol;Acc:HGNC:43324]","synonyms":"RN5S424","biotype":"rRNA","ncbi_id":"100873675","summary":null,"start":47450347,"end":47450461,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 424 [Source:HGNC Symbol;Acc:HGNC:43324]"}, {"versioned_ensembl_gene_id":"ENSG00000263681.1","gene_symbol":"MIR3197","gene_name":"microRNA 3197 [Source:HGNC Symbol;Acc:HGNC:38366]","synonyms":"hsa-mir-3197","biotype":"miRNA","ncbi_id":"100423023","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":41167557,"end":41167629,"strand":1,"description":"microRNA 3197 [Source:HGNC Symbol;Acc:HGNC:38366]"}, {"versioned_ensembl_gene_id":"ENSG00000202304.1","gene_symbol":"RNU6-1130P","gene_name":"RNA, U6 small nuclear 1130, pseudogene [Source:HGNC Symbol;Acc:HGNC:48093]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480063","summary":null,"start":130310072,"end":130310178,"strand":-1,"description":"RNA, U6 small nuclear 1130, pseudogene [Source:HGNC Symbol;Acc:HGNC:48093]"}, {"versioned_ensembl_gene_id":"ENSG00000283281.1","gene_symbol":"MIR7978","gene_name":"microRNA 7978 [Source:HGNC Symbol;Acc:HGNC:50113]","synonyms":"hsa-mir-7978","biotype":"miRNA","ncbi_id":"102465859","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":21464700,"end":21464758,"strand":-1,"description":"microRNA 7978 [Source:HGNC Symbol;Acc:HGNC:50113]"}, {"versioned_ensembl_gene_id":"ENSG00000265983.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32546409,"end":32546557,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000277205.1","gene_symbol":"U3","gene_name":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":148386174,"end":148386384,"strand":1,"description":"Small nucleolar RNA U3 [Source:RFAM;Acc:RF00012]"}, {"versioned_ensembl_gene_id":"ENSG00000221394.1","gene_symbol":"MIR1229","gene_name":"microRNA 1229 [Source:HGNC Symbol;Acc:HGNC:33924]","synonyms":"MIRN1229,hsa-mir-1229","biotype":"miRNA","ncbi_id":"100302156","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":179798278,"end":179798346,"strand":-1,"description":"microRNA 1229 [Source:HGNC Symbol;Acc:HGNC:33924]"}, {"versioned_ensembl_gene_id":"ENSG00000222685.1","gene_symbol":"RN7SKP119","gene_name":"RNA, 7SK small nuclear pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:45843]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481749","summary":null,"start":47359505,"end":47359777,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 119 [Source:HGNC Symbol;Acc:HGNC:45843]"}, {"versioned_ensembl_gene_id":"ENSG00000201210.1","gene_symbol":"RNA5SP139","gene_name":"RNA, 5S ribosomal pseudogene 139 [Source:HGNC Symbol;Acc:HGNC:43039]","synonyms":"RN5S139","biotype":"rRNA","ncbi_id":"100873407","summary":null,"start":127963608,"end":127963724,"strand":1,"description":"RNA, 5S ribosomal pseudogene 139 [Source:HGNC Symbol;Acc:HGNC:43039]"}, {"versioned_ensembl_gene_id":"ENSG00000265089.1","gene_symbol":"MIR4655","gene_name":"microRNA 4655 [Source:HGNC Symbol;Acc:HGNC:41754]","synonyms":"hsa-mir-4655","biotype":"miRNA","ncbi_id":"100616160","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":1844180,"end":1844253,"strand":-1,"description":"microRNA 4655 [Source:HGNC Symbol;Acc:HGNC:41754]"}, {"versioned_ensembl_gene_id":"ENSG00000199815.2","gene_symbol":"SNORA17","gene_name":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":8931506,"end":8931631,"strand":1,"description":"Small nucleolar RNA SNORA17 [Source:RFAM;Acc:RF00560]"}, {"versioned_ensembl_gene_id":"ENSG00000253064.1","gene_symbol":"RNU6-711P","gene_name":"RNA, U6 small nuclear 711, pseudogene [Source:HGNC Symbol;Acc:HGNC:47674]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479881","summary":null,"start":29424762,"end":29424867,"strand":-1,"description":"RNA, U6 small nuclear 711, pseudogene [Source:HGNC Symbol;Acc:HGNC:47674]"}, {"versioned_ensembl_gene_id":"ENSG00000199357.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23456371,"end":23456467,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207973.1","gene_symbol":"MIR589","gene_name":"microRNA 589 [Source:HGNC Symbol;Acc:HGNC:32845]","synonyms":"MIRN589,hsa-mir-589","biotype":"miRNA","ncbi_id":"693174","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":5495819,"end":5495917,"strand":-1,"description":"microRNA 589 [Source:HGNC Symbol;Acc:HGNC:32845]"}, {"versioned_ensembl_gene_id":"ENSG00000276577.1","gene_symbol":"RNU6-467P","gene_name":"RNA, U6 small nuclear 467, pseudogene [Source:HGNC Symbol;Acc:HGNC:47430]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479772","summary":null,"start":20323001,"end":20323110,"strand":1,"description":"RNA, U6 small nuclear 467, pseudogene [Source:HGNC Symbol;Acc:HGNC:47430]"}, {"versioned_ensembl_gene_id":"ENSG00000202471.1","gene_symbol":"RNU4-20P","gene_name":"RNA, U4 small nuclear 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46956]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479567","summary":null,"start":59586793,"end":59586943,"strand":-1,"description":"RNA, U4 small nuclear 20, pseudogene [Source:HGNC Symbol;Acc:HGNC:46956]"}, {"versioned_ensembl_gene_id":"ENSG00000244544.2","gene_symbol":"RN7SL446P","gene_name":"RNA, 7SL, cytoplasmic 446, pseudogene [Source:HGNC Symbol;Acc:HGNC:46462]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479385","summary":null,"start":152264150,"end":152264445,"strand":-1,"description":"RNA, 7SL, cytoplasmic 446, pseudogene [Source:HGNC Symbol;Acc:HGNC:46462]"}, {"versioned_ensembl_gene_id":"ENSG00000264426.1","gene_symbol":"MIR4283-1","gene_name":"microRNA 4283-1 [Source:HGNC Symbol;Acc:HGNC:38238]","synonyms":"hsa-mir-4283-1","biotype":"miRNA","ncbi_id":"100422917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":56955785,"end":56955864,"strand":-1,"description":"microRNA 4283-1 [Source:HGNC Symbol;Acc:HGNC:38238]"}, {"versioned_ensembl_gene_id":"ENSG00000252860.1","gene_symbol":"RNU6-570P","gene_name":"RNA, U6 small nuclear 570, pseudogene [Source:HGNC Symbol;Acc:HGNC:47533]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481361","summary":null,"start":200054061,"end":200054165,"strand":1,"description":"RNA, U6 small nuclear 570, pseudogene [Source:HGNC Symbol;Acc:HGNC:47533]"}, {"versioned_ensembl_gene_id":"ENSG00000202039.1","gene_symbol":"RNU6-215P","gene_name":"RNA, U6 small nuclear 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:47178]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481245","summary":null,"start":5180061,"end":5180162,"strand":1,"description":"RNA, U6 small nuclear 215, pseudogene [Source:HGNC Symbol;Acc:HGNC:47178]"}, {"versioned_ensembl_gene_id":"ENSG00000207741.1","gene_symbol":"MIR590","gene_name":"microRNA 590 [Source:HGNC Symbol;Acc:HGNC:32846]","synonyms":"hsa-mir-590,MIRN590","biotype":"miRNA","ncbi_id":"693175","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":74191198,"end":74191294,"strand":1,"description":"microRNA 590 [Source:HGNC Symbol;Acc:HGNC:32846]"}, {"versioned_ensembl_gene_id":"ENSG00000264346.1","gene_symbol":"SNORA77B","gene_name":"small nucleolar RNA, H/ACA box 77B [Source:HGNC Symbol;Acc:HGNC:52221]","synonyms":null,"biotype":"snoRNA","ncbi_id":"109617010","summary":null,"start":20126402,"end":20126526,"strand":1,"description":"small nucleolar RNA, H/ACA box 77B [Source:HGNC Symbol;Acc:HGNC:52221]"}, {"versioned_ensembl_gene_id":"ENSG00000274171.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":46366710,"end":46366990,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000276396.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":139155153,"end":139155444,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000199127.1","gene_symbol":"MIR383","gene_name":"microRNA 383 [Source:HGNC Symbol;Acc:HGNC:31876]","synonyms":"MIRN383,hsa-mir-383","biotype":"miRNA","ncbi_id":"494332","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":14853438,"end":14853510,"strand":-1,"description":"microRNA 383 [Source:HGNC Symbol;Acc:HGNC:31876]"}, {"versioned_ensembl_gene_id":"ENSG00000277483.1","gene_symbol":"RN7SL321P","gene_name":"RNA, 7SL, cytoplasmic 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:46337]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480501","summary":null,"start":48379834,"end":48380132,"strand":1,"description":"RNA, 7SL, cytoplasmic 321, pseudogene [Source:HGNC Symbol;Acc:HGNC:46337]"}, {"versioned_ensembl_gene_id":"ENSG00000278757.1","gene_symbol":"U6","gene_name":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":516376,"end":516479,"strand":-1,"description":"U6 spliceosomal RNA [Source:RFAM;Acc:RF00026]"}, {"versioned_ensembl_gene_id":"ENSG00000200882.1","gene_symbol":"RNU6-681P","gene_name":"RNA, U6 small nuclear 681, pseudogene [Source:HGNC Symbol;Acc:HGNC:47644]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481911","summary":null,"start":177126017,"end":177126120,"strand":-1,"description":"RNA, U6 small nuclear 681, pseudogene [Source:HGNC Symbol;Acc:HGNC:47644]"}, {"versioned_ensembl_gene_id":"ENSG00000252346.1","gene_symbol":"RNA5SP121","gene_name":"RNA, 5S ribosomal pseudogene 121 [Source:HGNC Symbol;Acc:HGNC:42919]","synonyms":"RN5S121","biotype":"rRNA","ncbi_id":"100873391","summary":null,"start":227763052,"end":227763152,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 121 [Source:HGNC Symbol;Acc:HGNC:42919]"}, {"versioned_ensembl_gene_id":"ENSG00000200360.1","gene_symbol":"RNU6-792P","gene_name":"RNA, U6 small nuclear 792, pseudogene [Source:HGNC Symbol;Acc:HGNC:47755]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481431","summary":null,"start":111490317,"end":111490423,"strand":-1,"description":"RNA, U6 small nuclear 792, pseudogene [Source:HGNC Symbol;Acc:HGNC:47755]"}, {"versioned_ensembl_gene_id":"ENSG00000206935.1","gene_symbol":"RNU6-514P","gene_name":"RNA, U6 small nuclear 514, pseudogene [Source:HGNC Symbol;Acc:HGNC:47477]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480586","summary":null,"start":23162704,"end":23162810,"strand":1,"description":"RNA, U6 small nuclear 514, pseudogene [Source:HGNC Symbol;Acc:HGNC:47477]"}, {"versioned_ensembl_gene_id":"ENSG00000284288.1","gene_symbol":"MIR378D2","gene_name":"microRNA 378d-2 [Source:HGNC Symbol;Acc:HGNC:41797]","synonyms":"hsa-mir-378d-2","biotype":"miRNA","ncbi_id":"100616169","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":93916022,"end":93916119,"strand":-1,"description":"microRNA 378d-2 [Source:HGNC Symbol;Acc:HGNC:41797]"}, {"versioned_ensembl_gene_id":"ENSG00000212466.1","gene_symbol":"RNU6-952P","gene_name":"RNA, U6 small nuclear 952, pseudogene [Source:HGNC Symbol;Acc:HGNC:47915]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479987","summary":null,"start":102313722,"end":102313829,"strand":1,"description":"RNA, U6 small nuclear 952, pseudogene [Source:HGNC Symbol;Acc:HGNC:47915]"}, {"versioned_ensembl_gene_id":"ENSG00000202254.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":99791662,"end":99791753,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284570.1","gene_symbol":"MIR7705","gene_name":"microRNA 7705 [Source:HGNC Symbol;Acc:HGNC:50143]","synonyms":"hsa-mir-7705","biotype":"miRNA","ncbi_id":"102466854","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":100702968,"end":100703024,"strand":-1,"description":"microRNA 7705 [Source:HGNC Symbol;Acc:HGNC:50143]"}, {"versioned_ensembl_gene_id":"ENSG00000223335.1","gene_symbol":"RNU6-603P","gene_name":"RNA, U6 small nuclear 603, pseudogene [Source:HGNC Symbol;Acc:HGNC:47566]","synonyms":"RNU6-825P","biotype":"snRNA","ncbi_id":"106480594","summary":null,"start":32352877,"end":32352983,"strand":1,"description":"RNA, U6 small nuclear 603, pseudogene [Source:HGNC Symbol;Acc:HGNC:47566]"}, {"versioned_ensembl_gene_id":"ENSG00000222761.1","gene_symbol":"RNU6-684P","gene_name":"RNA, U6 small nuclear 684, pseudogene [Source:HGNC Symbol;Acc:HGNC:47647]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481396","summary":null,"start":104400943,"end":104401048,"strand":-1,"description":"RNA, U6 small nuclear 684, pseudogene [Source:HGNC Symbol;Acc:HGNC:47647]"}, {"versioned_ensembl_gene_id":"ENSG00000215966.1","gene_symbol":"MIR876","gene_name":"microRNA 876 [Source:HGNC Symbol;Acc:HGNC:33653]","synonyms":"MIRN876,hsa-mir-876","biotype":"miRNA","ncbi_id":"100126310","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":28863626,"end":28863706,"strand":-1,"description":"microRNA 876 [Source:HGNC Symbol;Acc:HGNC:33653]"}, {"versioned_ensembl_gene_id":"ENSG00000263608.2","gene_symbol":"RN7SL353P","gene_name":"RNA, 7SL, cytoplasmic 353, pseudogene [Source:HGNC Symbol;Acc:HGNC:46369]","synonyms":"RN7SL579P","biotype":"misc_RNA","ncbi_id":"106481020","summary":null,"start":30751038,"end":30751289,"strand":1,"description":"RNA, 7SL, cytoplasmic 353, pseudogene [Source:HGNC Symbol;Acc:HGNC:46369]"}, {"versioned_ensembl_gene_id":"ENSG00000283863.1","gene_symbol":"MIR3960","gene_name":"microRNA 3960 [Source:HGNC Symbol;Acc:HGNC:41595]","synonyms":"hsa-mir-3960","biotype":"miRNA","ncbi_id":"100616250","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":127785833,"end":127785923,"strand":1,"description":"microRNA 3960 [Source:HGNC Symbol;Acc:HGNC:41595]"}, {"versioned_ensembl_gene_id":"ENSG00000277903.1","gene_symbol":"U2","gene_name":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":43271369,"end":43271559,"strand":-1,"description":"U2 spliceosomal RNA [Source:RFAM;Acc:RF00004]"}, {"versioned_ensembl_gene_id":"ENSG00000201618.1","gene_symbol":"RNA5SP505","gene_name":"RNA, 5S ribosomal pseudogene 505 [Source:HGNC Symbol;Acc:HGNC:43405]","synonyms":"RN5S505","biotype":"rRNA","ncbi_id":"100873556","summary":null,"start":53909054,"end":53909161,"strand":1,"description":"RNA, 5S ribosomal pseudogene 505 [Source:HGNC Symbol;Acc:HGNC:43405]"}, {"versioned_ensembl_gene_id":"ENSG00000237847.2","gene_symbol":"FAM231A","gene_name":"family with sequence similarity 231 member A [Source:HGNC Symbol;Acc:HGNC:49427]","synonyms":null,"biotype":"protein_coding","ncbi_id":"729574","summary":null,"start":16673003,"end":16673512,"strand":1,"description":"family with sequence similarity 231 member A [Source:HGNC Symbol;Acc:HGNC:49427]"}, {"versioned_ensembl_gene_id":"ENSG00000272080.1","gene_symbol":"MIR502","gene_name":"microRNA 502 [Source:HGNC Symbol;Acc:HGNC:32136]","synonyms":"MIRN502,hsa-mir-502","biotype":"miRNA","ncbi_id":"574504","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50014598,"end":50014683,"strand":1,"description":"microRNA 502 [Source:HGNC Symbol;Acc:HGNC:32136]"}, {"versioned_ensembl_gene_id":"ENSG00000278151.1","gene_symbol":"FAM13A-AS1_1","gene_name":"FAM13A antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02114]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":88710147,"end":88710265,"strand":1,"description":"FAM13A antisense RNA 1 conserved region 1 [Source:RFAM;Acc:RF02114]"}, {"versioned_ensembl_gene_id":"ENSG00000216060.1","gene_symbol":"MIR934","gene_name":"microRNA 934 [Source:HGNC Symbol;Acc:HGNC:33677]","synonyms":"MIRN934,hsa-mir-934","biotype":"miRNA","ncbi_id":"100126324","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":136550878,"end":136550960,"strand":1,"description":"microRNA 934 [Source:HGNC Symbol;Acc:HGNC:33677]"}, {"versioned_ensembl_gene_id":"ENSG00000238854.1","gene_symbol":"SNORD5","gene_name":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]","synonyms":"mgh28S-2410","biotype":"snoRNA","ncbi_id":"692072","summary":null,"start":141447475,"end":141447549,"strand":1,"description":"Small nucleolar RNA SNORD5 [Source:RFAM;Acc:RF01161]"}, {"versioned_ensembl_gene_id":"ENSG00000239137.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":55167171,"end":55167274,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000264251.2","gene_symbol":"RN7SL819P","gene_name":"RNA, 7SL, cytoplasmic 819, pseudogene [Source:HGNC 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[Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47557413,"end":47557514,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000212360.1","gene_symbol":"RNU6-1177P","gene_name":"RNA, U6 small nuclear 1177, pseudogene [Source:HGNC Symbol;Acc:HGNC:48140]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480645","summary":null,"start":61852499,"end":61852602,"strand":1,"description":"RNA, U6 small nuclear 1177, pseudogene [Source:HGNC Symbol;Acc:HGNC:48140]"}, {"versioned_ensembl_gene_id":"ENSG00000252745.1","gene_symbol":"RNA5SP143","gene_name":"RNA, 5S ribosomal pseudogene 143 [Source:HGNC Symbol;Acc:HGNC:43043]","synonyms":"RN5S143","biotype":"rRNA","ncbi_id":"100873410","summary":null,"start":142591677,"end":142591791,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 143 [Source:HGNC Symbol;Acc:HGNC:43043]"}, {"versioned_ensembl_gene_id":"ENSG00000212433.1","gene_symbol":"RNA5SP252","gene_name":"RNA, 5S ribosomal pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:43152]","synonyms":"RN5S252","biotype":"rRNA","ncbi_id":"100873508","summary":null,"start":10686569,"end":10686687,"strand":1,"description":"RNA, 5S ribosomal pseudogene 252 [Source:HGNC Symbol;Acc:HGNC:43152]"}, {"versioned_ensembl_gene_id":"ENSG00000251994.1","gene_symbol":"RNU2-27P","gene_name":"RNA, U2 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:48520]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481642","summary":null,"start":9518119,"end":9518260,"strand":-1,"description":"RNA, U2 small nuclear 27, pseudogene [Source:HGNC Symbol;Acc:HGNC:48520]"}, {"versioned_ensembl_gene_id":"ENSG00000252433.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":67102645,"end":67102779,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000244236.3","gene_symbol":"RN7SL604P","gene_name":"RNA, 7SL, cytoplasmic 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:46620]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479442","summary":null,"start":69516751,"end":69517046,"strand":1,"description":"RNA, 7SL, cytoplasmic 604, pseudogene [Source:HGNC Symbol;Acc:HGNC:46620]"}, {"versioned_ensembl_gene_id":"ENSG00000275780.1","gene_symbol":"RNA5SP443","gene_name":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]","synonyms":"RN5S443","biotype":"rRNA","ncbi_id":"106481745","summary":null,"start":45327366,"end":45327497,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 443 [Source:HGNC Symbol;Acc:HGNC:43343]"}, {"versioned_ensembl_gene_id":"ENSG00000202112.1","gene_symbol":"RNU6-690P","gene_name":"RNA, U6 small nuclear 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:47653]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481398","summary":null,"start":95599114,"end":95599219,"strand":1,"description":"RNA, U6 small nuclear 690, pseudogene [Source:HGNC Symbol;Acc:HGNC:47653]"}, {"versioned_ensembl_gene_id":"ENSG00000274467.1","gene_symbol":"RNA5SP257","gene_name":"RNA, 5S ribosomal pseudogene 257 [Source:HGNC Symbol;Acc:HGNC:43157]","synonyms":"RN5S257","biotype":"rRNA","ncbi_id":"100873511","summary":null,"start":20290174,"end":20290289,"strand":1,"description":"RNA, 5S ribosomal pseudogene 257 [Source:HGNC Symbol;Acc:HGNC:43157]"}, {"versioned_ensembl_gene_id":"ENSG00000253015.1","gene_symbol":"RN7SKP64","gene_name":"RNA, 7SK small nuclear pseudogene 64 [Source:HGNC 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The family member CHRNA7, which is located on chromosome 15 in a region associated with several neuropsychiatric disorders, is partially duplicated and forms a hybrid with a novel gene from the family with sequence similarity 7 (FAM7A). Alternative splicing has been observed, and two variants exist, for this hybrid gene. The N-terminally truncated products predicted by the largest open reading frames for each variant would lack the majority of the neurotransmitter-gated ion-channel ligand binding domain but retain the transmembrane region that forms the ion channel. Although current evidence supports transcription of this hybrid gene, translation of the nicotinic acetylcholine receptor-like protein-encoding open reading frames has not been confirmed. [provided by RefSeq, Jul 2008]","start":30511927,"end":30544252,"strand":-1,"description":"CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion [Source:HGNC Symbol;Acc:HGNC:15781]"}, {"versioned_ensembl_gene_id":"ENSG00000199285.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38987281,"end":38987383,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000206638.1","gene_symbol":"RNU6-672P","gene_name":"RNA, U6 small nuclear 672, pseudogene [Source:HGNC Symbol;Acc:HGNC:47635]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481910","summary":null,"start":72869544,"end":72869650,"strand":-1,"description":"RNA, U6 small nuclear 672, pseudogene [Source:HGNC Symbol;Acc:HGNC:47635]"}, {"versioned_ensembl_gene_id":"ENSG00000208308.1","gene_symbol":"SNORA40B","gene_name":"small nucleolar RNA, H/ACA box 40B [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000252321.1","gene_symbol":"RN7SKP83","gene_name":"RNA, 7SK small nuclear pseudogene 83 [Source:HGNC Symbol;Acc:HGNC:45807]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479131","summary":null,"start":85820435,"end":85820612,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 83 [Source:HGNC Symbol;Acc:HGNC:45807]"}, {"versioned_ensembl_gene_id":"ENSG00000252524.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":157064557,"end":157064663,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207258.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":38744020,"end":38744131,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252519.1","gene_symbol":"RNU6-783P","gene_name":"RNA, U6 small nuclear 783, pseudogene [Source:HGNC Symbol;Acc:HGNC:47746]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479912","summary":null,"start":23849778,"end":23849882,"strand":1,"description":"RNA, U6 small nuclear 783, pseudogene [Source:HGNC Symbol;Acc:HGNC:47746]"}, {"versioned_ensembl_gene_id":"ENSG00000265838.1","gene_symbol":"U1","gene_name":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":32539820,"end":32539971,"strand":-1,"description":"U1 spliceosomal RNA [Source:RFAM;Acc:RF00003]"}, {"versioned_ensembl_gene_id":"ENSG00000243173.3","gene_symbol":"RN7SL861P","gene_name":"RNA, 7SL, cytoplasmic 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:46877]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479534","summary":null,"start":162777730,"end":162778014,"strand":1,"description":"RNA, 7SL, cytoplasmic 861, pseudogene [Source:HGNC Symbol;Acc:HGNC:46877]"}, {"versioned_ensembl_gene_id":"ENSG00000252204.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":31811088,"end":31811190,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000207037.1","gene_symbol":"RNU6-339P","gene_name":"RNA, U6 small nuclear 339, pseudogene [Source:HGNC Symbol;Acc:HGNC:47302]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481888","summary":null,"start":84938416,"end":84938522,"strand":-1,"description":"RNA, U6 small nuclear 339, pseudogene [Source:HGNC Symbol;Acc:HGNC:47302]"}, {"versioned_ensembl_gene_id":"ENSG00000251714.1","gene_symbol":"RN7SKP67","gene_name":"RNA, 7SK small nuclear pseudogene 67 [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000206865.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":56753226,"end":56753326,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252762.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":81928313,"end":81928439,"strand":1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000199289.1","gene_symbol":"RNU6-502P","gene_name":"RNA, U6 small nuclear 502, pseudogene [Source:HGNC Symbol;Acc:HGNC:47465]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481899","summary":null,"start":26519351,"end":26519458,"strand":-1,"description":"RNA, U6 small nuclear 502, pseudogene [Source:HGNC Symbol;Acc:HGNC:47465]"}, {"versioned_ensembl_gene_id":"ENSG00000222102.1","gene_symbol":"RN7SKP232","gene_name":"RNA, 7SK small nuclear pseudogene 232 [Source:HGNC Symbol;Acc:HGNC:45956]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480905","summary":null,"start":151704289,"end":151704578,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 232 [Source:HGNC Symbol;Acc:HGNC:45956]"}, {"versioned_ensembl_gene_id":"ENSG00000238862.1","gene_symbol":"SNORD19B","gene_name":"small nucleolar RNA, C/D box 19B [Source:HGNC Symbol;Acc:HGNC:33570]","synonyms":null,"biotype":"snoRNA","ncbi_id":"100113381","summary":null,"start":52690744,"end":52690827,"strand":1,"description":"small nucleolar RNA, C/D box 19B [Source:HGNC Symbol;Acc:HGNC:33570]"}, {"versioned_ensembl_gene_id":"ENSG00000201869.1","gene_symbol":"RNU6-294P","gene_name":"RNA, U6 small nuclear 294, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000199395.1","gene_symbol":"RNA5SP93","gene_name":"RNA, 5S ribosomal pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:42891]","synonyms":"RN5S93","biotype":"rRNA","ncbi_id":"100873326","summary":null,"start":56235217,"end":56235330,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 93 [Source:HGNC Symbol;Acc:HGNC:42891]"}, {"versioned_ensembl_gene_id":"ENSG00000200397.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":87218611,"end":87218712,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277923.4","gene_symbol":"MBOAT7","gene_name":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]","synonyms":"BB1,LPIAT,LENG4,hMBOA-7,BB1,LPIAT,LENG4,hMBOA-7","biotype":"protein_coding","ncbi_id":"79143","summary":"This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]","start":54173854,"end":54190480,"strand":-1,"description":"membrane bound O-acyltransferase domain containing 7 [Source:HGNC Symbol;Acc:HGNC:15505]"}, {"versioned_ensembl_gene_id":"ENSG00000201570.1","gene_symbol":"RNU4-56P","gene_name":"RNA, U4 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:46992]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480547","summary":null,"start":39970125,"end":39970266,"strand":1,"description":"RNA, U4 small nuclear 56, pseudogene [Source:HGNC Symbol;Acc:HGNC:46992]"}, {"versioned_ensembl_gene_id":"ENSG00000252673.1","gene_symbol":"RNA5SP421","gene_name":"RNA, 5S ribosomal pseudogene 421 [Source:HGNC Symbol;Acc:HGNC:43321]","synonyms":"RN5S421","biotype":"rRNA","ncbi_id":"100873672","summary":null,"start":35754555,"end":35754688,"strand":1,"description":"RNA, 5S ribosomal pseudogene 421 [Source:HGNC Symbol;Acc:HGNC:43321]"}, {"versioned_ensembl_gene_id":"ENSG00000199812.1","gene_symbol":"RNU6-428P","gene_name":"RNA, U6 small nuclear 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:47391]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481894","summary":null,"start":146571477,"end":146571583,"strand":1,"description":"RNA, U6 small nuclear 428, pseudogene [Source:HGNC Symbol;Acc:HGNC:47391]"}, {"versioned_ensembl_gene_id":"ENSG00000201160.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":25697076,"end":25697188,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201554.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":101458530,"end":101458626,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000253024.1","gene_symbol":"RNU6-1238P","gene_name":"RNA, U6 small nuclear 1238, pseudogene [Source:HGNC Symbol;Acc:HGNC:48201]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480107","summary":null,"start":67395210,"end":67395311,"strand":-1,"description":"RNA, U6 small nuclear 1238, pseudogene [Source:HGNC Symbol;Acc:HGNC:48201]"}, {"versioned_ensembl_gene_id":"ENSG00000264371.1","gene_symbol":"MIR4425","gene_name":"microRNA 4425 [Source:HGNC Symbol;Acc:HGNC:41891]","synonyms":"hsa-mir-4425","biotype":"miRNA","ncbi_id":"100616365","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":25023503,"end":25023586,"strand":1,"description":"microRNA 4425 [Source:HGNC Symbol;Acc:HGNC:41891]"}, {"versioned_ensembl_gene_id":"ENSG00000252815.1","gene_symbol":"RNU6-410P","gene_name":"RNA, U6 small nuclear 410, pseudogene [Source:HGNC Symbol;Acc:HGNC:47373]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481893","summary":null,"start":55031965,"end":55032071,"strand":-1,"description":"RNA, U6 small nuclear 410, pseudogene [Source:HGNC Symbol;Acc:HGNC:47373]"}, {"versioned_ensembl_gene_id":"ENSG00000252854.1","gene_symbol":"RN7SKP5","gene_name":"RNA, 7SK small nuclear pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42623]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"100873849","summary":null,"start":46249942,"end":46250213,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:42623]"}, {"versioned_ensembl_gene_id":"ENSG00000251895.1","gene_symbol":"RNU6-976P","gene_name":"RNA, U6 small nuclear 976, pseudogene [Source:HGNC Symbol;Acc:HGNC:47939]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481488","summary":null,"start":84739942,"end":84740052,"strand":1,"description":"RNA, U6 small nuclear 976, pseudogene [Source:HGNC Symbol;Acc:HGNC:47939]"}, {"versioned_ensembl_gene_id":"ENSG00000266676.1","gene_symbol":"MIR4297","gene_name":"microRNA 4297 [Source:HGNC Symbol;Acc:HGNC:38393]","synonyms":"hsa-mir-4297","biotype":"miRNA","ncbi_id":"100422873","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":129843299,"end":129843374,"strand":-1,"description":"microRNA 4297 [Source:HGNC Symbol;Acc:HGNC:38393]"}, {"versioned_ensembl_gene_id":"ENSG00000264947.1","gene_symbol":"MIR3181","gene_name":"microRNA 3181 [Source:HGNC Symbol;Acc:HGNC:38378]","synonyms":"hsa-mir-3181","biotype":"miRNA","ncbi_id":"100422972","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50742305,"end":50742377,"strand":1,"description":"microRNA 3181 [Source:HGNC Symbol;Acc:HGNC:38378]"}, {"versioned_ensembl_gene_id":"ENSG00000226572.1","gene_symbol":"SNORD57","gene_name":"small nucleolar RNA, C/D box 57 [Source:HGNC Symbol;Acc:HGNC:10207]","synonyms":"U57,RNU57","biotype":"snoRNA","ncbi_id":"26792","summary":null,"start":2656939,"end":2657010,"strand":1,"description":"small nucleolar RNA, C/D box 57 [Source:HGNC Symbol;Acc:HGNC:10207]"}, {"versioned_ensembl_gene_id":"ENSG00000208017.3","gene_symbol":"MIR140","gene_name":"microRNA 140 [Source:HGNC Symbol;Acc:HGNC:31527]","synonyms":"MIRN140,hsa-mir-140","biotype":"miRNA","ncbi_id":"406932","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":69933081,"end":69933180,"strand":1,"description":"microRNA 140 [Source:HGNC Symbol;Acc:HGNC:31527]"}, {"versioned_ensembl_gene_id":"ENSG00000264511.1","gene_symbol":"MIR3678","gene_name":"microRNA 3678 [Source:HGNC Symbol;Acc:HGNC:38891]","synonyms":"hsa-mir-3678","biotype":"miRNA","ncbi_id":"100500841","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":75406069,"end":75406162,"strand":1,"description":"microRNA 3678 [Source:HGNC Symbol;Acc:HGNC:38891]"}, {"versioned_ensembl_gene_id":"ENSG00000222767.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":47313027,"end":47313121,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284568.1","gene_symbol":"MIR371B","gene_name":"microRNA 371b [Source:HGNC Symbol;Acc:HGNC:41863]","synonyms":"hsa-mir-371b","biotype":"miRNA","ncbi_id":"100616185","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":53787677,"end":53787742,"strand":-1,"description":"microRNA 371b [Source:HGNC Symbol;Acc:HGNC:41863]"}, {"versioned_ensembl_gene_id":"ENSG00000266738.1","gene_symbol":"MIR4757","gene_name":"microRNA 4757 [Source:HGNC Symbol;Acc:HGNC:41746]","synonyms":"hsa-mir-4757","biotype":"miRNA","ncbi_id":"100616307","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":19348429,"end":19348505,"strand":1,"description":"microRNA 4757 [Source:HGNC Symbol;Acc:HGNC:41746]"}, {"versioned_ensembl_gene_id":"ENSG00000265411.1","gene_symbol":"RN7SL656P","gene_name":"RNA, 7SL, cytoplasmic 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:46672]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481760","summary":null,"start":46319679,"end":46319959,"strand":1,"description":"RNA, 7SL, cytoplasmic 656, pseudogene [Source:HGNC Symbol;Acc:HGNC:46672]"}, {"versioned_ensembl_gene_id":"ENSG00000252369.1","gene_symbol":"RNU7-51P","gene_name":"RNA, U7 small nuclear 51 pseudogene [Source:HGNC Symbol;Acc:HGNC:34147]","synonyms":"U7.51","biotype":"snRNA","ncbi_id":"100151647","summary":null,"start":83048579,"end":83048640,"strand":1,"description":"RNA, U7 small nuclear 51 pseudogene [Source:HGNC Symbol;Acc:HGNC:34147]"}, {"versioned_ensembl_gene_id":"ENSG00000207923.1","gene_symbol":"MIR559","gene_name":"microRNA 559 [Source:HGNC Symbol;Acc:HGNC:32815]","synonyms":"MIRN559,hsa-mir-559","biotype":"miRNA","ncbi_id":"693144","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":47377675,"end":47377770,"strand":1,"description":"microRNA 559 [Source:HGNC Symbol;Acc:HGNC:32815]"}, {"versioned_ensembl_gene_id":"ENSG00000283637.1","gene_symbol":"hsa-mir-4776-1","gene_name":"hsa-mir-4776-1 [Source:miRBase;Acc:MI0017419]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":212926257,"end":212926336,"strand":-1,"description":"hsa-mir-4776-1 [Source:miRBase;Acc:MI0017419]"}, {"versioned_ensembl_gene_id":"ENSG00000201516.1","gene_symbol":"SNORA51","gene_name":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]","synonyms":"ACA51","biotype":"snoRNA","ncbi_id":"677831","summary":null,"start":176098163,"end":176098285,"strand":1,"description":"Small nucleolar RNA SNORA51 [Source:RFAM;Acc:RF00432]"}, {"versioned_ensembl_gene_id":"ENSG00000266887.1","gene_symbol":"MIR4535","gene_name":"microRNA 4535 [Source:HGNC Symbol;Acc:HGNC:41629]","synonyms":"hsa-mir-4535","biotype":"miRNA","ncbi_id":"100616415","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48780295,"end":48780353,"strand":1,"description":"microRNA 4535 [Source:HGNC Symbol;Acc:HGNC:41629]"}, {"versioned_ensembl_gene_id":"ENSG00000199075.1","gene_symbol":"MIR26A1","gene_name":"microRNA 26a-1 [Source:HGNC Symbol;Acc:HGNC:31610]","synonyms":"MIRN26A1,hsa-mir-26a-1","biotype":"miRNA","ncbi_id":"407015","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":37969404,"end":37969480,"strand":1,"description":"microRNA 26a-1 [Source:HGNC Symbol;Acc:HGNC:31610]"}, {"versioned_ensembl_gene_id":"ENSG00000284078.1","gene_symbol":"hsa-mir-3607","gene_name":"hsa-mir-3607 [Source:miRBase;Acc:MI0015997]","synonyms":null,"biotype":"miRNA","ncbi_id":null,"summary":null,"start":86620497,"end":86620575,"strand":1,"description":"hsa-mir-3607 [Source:miRBase;Acc:MI0015997]"}, {"versioned_ensembl_gene_id":"ENSG00000275227.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":25618132,"end":25618312,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000221287.1","gene_symbol":"MIR1289-2","gene_name":"microRNA 1289-2 [Source:HGNC Symbol;Acc:HGNC:35282]","synonyms":"MIRN1289-2,hsa-mir-1289-2","biotype":"miRNA","ncbi_id":"100302134","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":133427596,"end":133427706,"strand":-1,"description":"microRNA 1289-2 [Source:HGNC Symbol;Acc:HGNC:35282]"}, {"versioned_ensembl_gene_id":"ENSG00000284517.1","gene_symbol":"MIR6873","gene_name":"microRNA 6873 [Source:HGNC Symbol;Acc:HGNC:50231]","synonyms":"hsa-mir-6873","biotype":"miRNA","ncbi_id":"102466754","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":33287227,"end":33287289,"strand":-1,"description":"microRNA 6873 [Source:HGNC Symbol;Acc:HGNC:50231]"}, {"versioned_ensembl_gene_id":"ENSG00000242241.3","gene_symbol":"RN7SL306P","gene_name":"RNA, 7SL, cytoplasmic 306, pseudogene [Source:HGNC Symbol;Acc:HGNC:46322]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481006","summary":null,"start":128970734,"end":128971029,"strand":1,"description":"RNA, 7SL, cytoplasmic 306, pseudogene [Source:HGNC Symbol;Acc:HGNC:46322]"}, {"versioned_ensembl_gene_id":"ENSG00000252960.1","gene_symbol":"RN7SKP258","gene_name":"RNA, 7SK small nuclear pseudogene 258 [Source:HGNC Symbol;Acc:HGNC:45982]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480912","summary":null,"start":18651147,"end":18651450,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 258 [Source:HGNC Symbol;Acc:HGNC:45982]"}, {"versioned_ensembl_gene_id":"ENSG00000221060.1","gene_symbol":"SNORA11","gene_name":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]","synonyms":"SNORA11A,U107","biotype":"snoRNA","ncbi_id":"677799","summary":"Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]","start":69804203,"end":69804331,"strand":-1,"description":"Small nucleolar RNA SNORA11 [Source:RFAM;Acc:RF00614]"}, {"versioned_ensembl_gene_id":"ENSG00000252866.1","gene_symbol":"RNA5SP243","gene_name":"RNA, 5S ribosomal pseudogene 243 [Source:HGNC Symbol;Acc:HGNC:43143]","synonyms":"RN5S243","biotype":"rRNA","ncbi_id":"106479001","summary":null,"start":128697710,"end":128697744,"strand":1,"description":"RNA, 5S ribosomal pseudogene 243 [Source:HGNC Symbol;Acc:HGNC:43143]"}, {"versioned_ensembl_gene_id":"ENSG00000207371.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":41917416,"end":41917526,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000277138.1","gene_symbol":"MIR6509","gene_name":"microRNA 6509 [Source:HGNC Symbol;Acc:HGNC:50207]","synonyms":"hsa-mir-6509","biotype":"miRNA","ncbi_id":"102465254","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":135206994,"end":135207078,"strand":-1,"description":"microRNA 6509 [Source:HGNC Symbol;Acc:HGNC:50207]"}, {"versioned_ensembl_gene_id":"ENSG00000221442.1","gene_symbol":"MIR548F4","gene_name":"microRNA 548f-4 [Source:HGNC Symbol;Acc:HGNC:35308]","synonyms":"MIRN548F4,hsa-mir-548f-4","biotype":"miRNA","ncbi_id":"100313895","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":147378017,"end":147378121,"strand":-1,"description":"microRNA 548f-4 [Source:HGNC Symbol;Acc:HGNC:35308]"}, {"versioned_ensembl_gene_id":"ENSG00000237261.2","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":14530941,"end":14531223,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283327.1","gene_symbol":"MIR6841","gene_name":"microRNA 6841 [Source:HGNC Symbol;Acc:HGNC:50070]","synonyms":"hsa-mir-6841","biotype":"miRNA","ncbi_id":"102465506","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":24953796,"end":24953867,"strand":-1,"description":"microRNA 6841 [Source:HGNC Symbol;Acc:HGNC:50070]"}, {"versioned_ensembl_gene_id":"ENSG00000207970.3","gene_symbol":"MIR660","gene_name":"microRNA 660 [Source:HGNC Symbol;Acc:HGNC:32916]","synonyms":"MIRN660,hsa-mir-660","biotype":"miRNA","ncbi_id":"724030","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":50013241,"end":50013337,"strand":1,"description":"microRNA 660 [Source:HGNC Symbol;Acc:HGNC:32916]"}, {"versioned_ensembl_gene_id":"ENSG00000275978.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":34659564,"end":34659878,"strand":-1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000222934.1","gene_symbol":"RN7SKP284","gene_name":"RNA, 7SK small nuclear pseudogene 284 [Source:HGNC Symbol;Acc:HGNC:46008]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479222","summary":null,"start":86362132,"end":86362474,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 284 [Source:HGNC Symbol;Acc:HGNC:46008]"}, {"versioned_ensembl_gene_id":"ENSG00000200536.1","gene_symbol":"SNORA25","gene_name":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]","synonyms":"SNORA25A,ACA25","biotype":"snoRNA","ncbi_id":"684959","summary":null,"start":110272484,"end":110272607,"strand":1,"description":"Small nucleolar RNA SNORA25 [Source:RFAM;Acc:RF00402]"}, {"versioned_ensembl_gene_id":"ENSG00000222099.1","gene_symbol":"RN7SKP32","gene_name":"RNA, 7SK small nuclear pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:45756]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479109","summary":null,"start":47068021,"end":47068323,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 32 [Source:HGNC Symbol;Acc:HGNC:45756]"}, {"versioned_ensembl_gene_id":"ENSG00000253053.1","gene_symbol":"RN7SKP289","gene_name":"RNA, 7SK small nuclear pseudogene 289 [Source:HGNC Symbol;Acc:HGNC:46013]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479224","summary":null,"start":53816185,"end":53816479,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 289 [Source:HGNC Symbol;Acc:HGNC:46013]"}, {"versioned_ensembl_gene_id":"ENSG00000263999.2","gene_symbol":"RN7SL42P","gene_name":"RNA, 7SL, cytoplasmic 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46058]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479240","summary":null,"start":59214406,"end":59214699,"strand":-1,"description":"RNA, 7SL, cytoplasmic 42, pseudogene [Source:HGNC Symbol;Acc:HGNC:46058]"}, {"versioned_ensembl_gene_id":"ENSG00000212571.1","gene_symbol":"RNA5SP482","gene_name":"RNA, 5S ribosomal pseudogene 482 [Source:HGNC Symbol;Acc:HGNC:43382]","synonyms":"RN5S482","biotype":"rRNA","ncbi_id":"100873724","summary":null,"start":32050588,"end":32050705,"strand":1,"description":"RNA, 5S ribosomal pseudogene 482 [Source:HGNC Symbol;Acc:HGNC:43382]"}, {"versioned_ensembl_gene_id":"ENSG00000201398.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":154007367,"end":154007502,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000202417.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":132945342,"end":132945454,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000222601.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":120504571,"end":120504659,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000207158.1","gene_symbol":"RNU6-929P","gene_name":"RNA, U6 small nuclear 929, pseudogene [Source:HGNC Symbol;Acc:HGNC:47892]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481473","summary":null,"start":56785981,"end":56786087,"strand":-1,"description":"RNA, U6 small nuclear 929, pseudogene [Source:HGNC Symbol;Acc:HGNC:47892]"}, {"versioned_ensembl_gene_id":"ENSG00000202248.1","gene_symbol":"RNA5SP85","gene_name":"RNA, 5S ribosomal pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:42883]","synonyms":"RN5S85","biotype":"rRNA","ncbi_id":"100873318","summary":null,"start":11561661,"end":11561779,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 85 [Source:HGNC Symbol;Acc:HGNC:42883]"}, {"versioned_ensembl_gene_id":"ENSG00000222092.1","gene_symbol":"RNU6-908P","gene_name":"RNA, U6 small nuclear 908, pseudogene [Source:HGNC Symbol;Acc:HGNC:47871]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479968","summary":null,"start":29711915,"end":29712008,"strand":1,"description":"RNA, U6 small nuclear 908, pseudogene [Source:HGNC Symbol;Acc:HGNC:47871]"}, {"versioned_ensembl_gene_id":"ENSG00000223013.1","gene_symbol":"RNA5SP344","gene_name":"RNA, 5S ribosomal pseudogene 344 [Source:HGNC 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Symbol;Acc:HGNC:46574]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481074","summary":null,"start":39761000,"end":39761298,"strand":1,"description":"RNA, 7SL, cytoplasmic 558, pseudogene [Source:HGNC Symbol;Acc:HGNC:46574]"}, {"versioned_ensembl_gene_id":"ENSG00000201684.1","gene_symbol":"RN7SKP239","gene_name":"RNA, 7SK small nuclear pseudogene 239 [Source:HGNC Symbol;Acc:HGNC:45963]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480907","summary":null,"start":67362414,"end":67362708,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 239 [Source:HGNC Symbol;Acc:HGNC:45963]"}, {"versioned_ensembl_gene_id":"ENSG00000199315.1","gene_symbol":"RNA5SP347","gene_name":"RNA, 5S ribosomal pseudogene 347 [Source:HGNC Symbol;Acc:HGNC:43247]","synonyms":"RN5S347","biotype":"rRNA","ncbi_id":"100873609","summary":null,"start":97657464,"end":97657582,"strand":1,"description":"RNA, 5S ribosomal pseudogene 347 [Source:HGNC Symbol;Acc:HGNC:43247]"}, {"versioned_ensembl_gene_id":"ENSG00000200528.1","gene_symbol":"RNU6-1331P","gene_name":"RNA, U6 small nuclear 1331, pseudogene [Source:HGNC Symbol;Acc:HGNC:48294]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480147","summary":null,"start":53914719,"end":53914824,"strand":1,"description":"RNA, U6 small nuclear 1331, pseudogene [Source:HGNC Symbol;Acc:HGNC:48294]"}, {"versioned_ensembl_gene_id":"ENSG00000207507.1","gene_symbol":"RNU6-9","gene_name":"RNA, U6 small nuclear 9 [Source:HGNC Symbol;Acc:HGNC:34269]","synonyms":"U6-9","biotype":"snRNA","ncbi_id":"101954271","summary":null,"start":893484,"end":893590,"strand":1,"description":"RNA, U6 small nuclear 9 [Source:HGNC Symbol;Acc:HGNC:34269]"}, {"versioned_ensembl_gene_id":"ENSG00000252333.1","gene_symbol":"RNU6-964P","gene_name":"RNA, U6 small nuclear 964, pseudogene [Source:HGNC Symbol;Acc:HGNC:47927]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479992","summary":null,"start":229937814,"end":229937882,"strand":-1,"description":"RNA, U6 small nuclear 964, pseudogene [Source:HGNC Symbol;Acc:HGNC:47927]"}, {"versioned_ensembl_gene_id":"ENSG00000251888.1","gene_symbol":"RN7SKP190","gene_name":"RNA, 7SK small nuclear pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:45914]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480891","summary":null,"start":82192505,"end":82192790,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 190 [Source:HGNC Symbol;Acc:HGNC:45914]"}, {"versioned_ensembl_gene_id":"ENSG00000281805.1","gene_symbol":"AL627082.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26647447,"end":26647681,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000223181.1","gene_symbol":"RNU6-1199P","gene_name":"RNA, U6 small nuclear 1199, pseudogene [Source:HGNC Symbol;Acc:HGNC:48162]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480091","summary":null,"start":758233,"end":758336,"strand":-1,"description":"RNA, U6 small nuclear 1199, pseudogene [Source:HGNC Symbol;Acc:HGNC:48162]"}, {"versioned_ensembl_gene_id":"ENSG00000222238.1","gene_symbol":"RNU2-43P","gene_name":"RNA, U2 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:48536]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480216","summary":null,"start":101307529,"end":101307718,"strand":1,"description":"RNA, U2 small nuclear 43, pseudogene [Source:HGNC Symbol;Acc:HGNC:48536]"}, {"versioned_ensembl_gene_id":"ENSG00000277948.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":175092401,"end":175092587,"strand":-1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000242113.3","gene_symbol":"RN7SL124P","gene_name":"RNA, 7SL, cytoplasmic 124, pseudogene [Source:HGNC Symbol;Acc:HGNC:46140]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480955","summary":null,"start":151372003,"end":151372287,"strand":1,"description":"RNA, 7SL, cytoplasmic 124, pseudogene [Source:HGNC Symbol;Acc:HGNC:46140]"}, {"versioned_ensembl_gene_id":"ENSG00000200750.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":21724119,"end":21724229,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000252429.2","gene_symbol":"RNU7-29P","gene_name":"RNA, U7 small nuclear 29 pseudogene [Source:HGNC Symbol;Acc:HGNC:34125]","synonyms":"U7.29","biotype":"snRNA","ncbi_id":"100147816","summary":null,"start":26602369,"end":26602432,"strand":-1,"description":"RNA, U7 small nuclear 29 pseudogene [Source:HGNC Symbol;Acc:HGNC:34125]"}, {"versioned_ensembl_gene_id":"ENSG00000252783.1","gene_symbol":"RNU6-835P","gene_name":"RNA, U6 small nuclear 835, pseudogene [Source:HGNC Symbol;Acc:HGNC:47798]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481445","summary":null,"start":87996345,"end":87996448,"strand":-1,"description":"RNA, U6 small nuclear 835, pseudogene [Source:HGNC Symbol;Acc:HGNC:47798]"}, {"versioned_ensembl_gene_id":"ENSG00000206991.1","gene_symbol":"RNU6-610P","gene_name":"RNA, U6 small nuclear 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:47573]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479835","summary":null,"start":43637632,"end":43637738,"strand":-1,"description":"RNA, U6 small nuclear 610, pseudogene [Source:HGNC Symbol;Acc:HGNC:47573]"}, {"versioned_ensembl_gene_id":"ENSG00000207181.1","gene_symbol":"SNORA14B","gene_name":"small nucleolar RNA, H/ACA box 14B [Source:HGNC Symbol;Acc:HGNC:32603]","synonyms":"ACA14b","biotype":"snoRNA","ncbi_id":"677802","summary":"Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 7. [provided by RefSeq, Oct 2008]","start":235127803,"end":235127937,"strand":-1,"description":"small nucleolar RNA, H/ACA box 14B [Source:HGNC Symbol;Acc:HGNC:32603]"}, {"versioned_ensembl_gene_id":"ENSG00000222303.1","gene_symbol":"RNU6-935P","gene_name":"RNA, U6 small nuclear 935, pseudogene [Source:HGNC Symbol;Acc:HGNC:47898]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480403","summary":null,"start":50649641,"end":50649740,"strand":1,"description":"RNA, U6 small nuclear 935, pseudogene [Source:HGNC Symbol;Acc:HGNC:47898]"}, {"versioned_ensembl_gene_id":"ENSG00000273975.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":201097744,"end":201098091,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000244671.3","gene_symbol":"RN7SL280P","gene_name":"RNA, 7SL, cytoplasmic 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:46296]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480498","summary":null,"start":21722895,"end":21723182,"strand":-1,"description":"RNA, 7SL, cytoplasmic 280, pseudogene [Source:HGNC Symbol;Acc:HGNC:46296]"}, {"versioned_ensembl_gene_id":"ENSG00000199509.1","gene_symbol":"RNA5SP477","gene_name":"RNA, 5S ribosomal pseudogene 477 [Source:HGNC Symbol;Acc:HGNC:43377]","synonyms":"RN5S477","biotype":"rRNA","ncbi_id":"100873719","summary":null,"start":21138956,"end":21139074,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 477 [Source:HGNC Symbol;Acc:HGNC:43377]"}, {"versioned_ensembl_gene_id":"ENSG00000201728.1","gene_symbol":"RNA5SP479","gene_name":"RNA, 5S ribosomal pseudogene 479 [Source:HGNC Symbol;Acc:HGNC:43379]","synonyms":"RN5S479","biotype":"rRNA","ncbi_id":"100873721","summary":null,"start":23380896,"end":23381012,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 479 [Source:HGNC Symbol;Acc:HGNC:43379]"}, {"versioned_ensembl_gene_id":"ENSG00000207382.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":62661621,"end":62661725,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000199385.1","gene_symbol":"RNU6-369P","gene_name":"RNA, U6 small nuclear 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:47332]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479730","summary":null,"start":44390722,"end":44390823,"strand":1,"description":"RNA, U6 small nuclear 369, pseudogene [Source:HGNC Symbol;Acc:HGNC:47332]"}, {"versioned_ensembl_gene_id":"ENSG00000207312.1","gene_symbol":"RNU6-429P","gene_name":"RNA, U6 small nuclear 429, pseudogene [Source:HGNC Symbol;Acc:HGNC:47392]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479755","summary":null,"start":11027200,"end":11027307,"strand":1,"description":"RNA, U6 small nuclear 429, pseudogene [Source:HGNC Symbol;Acc:HGNC:47392]"}, {"versioned_ensembl_gene_id":"ENSG00000239888.3","gene_symbol":"RN7SL792P","gene_name":"RNA, 7SL, cytoplasmic 792, pseudogene [Source:HGNC Symbol;Acc:HGNC:46808]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479509","summary":null,"start":15408384,"end":15408688,"strand":1,"description":"RNA, 7SL, cytoplasmic 792, pseudogene [Source:HGNC Symbol;Acc:HGNC:46808]"}, {"versioned_ensembl_gene_id":"ENSG00000252396.1","gene_symbol":"RN7SKP195","gene_name":"RNA, 7SK small nuclear pseudogene 195 [Source:HGNC Symbol;Acc:HGNC:45919]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481816","summary":null,"start":237120807,"end":237121109,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 195 [Source:HGNC Symbol;Acc:HGNC:45919]"}, {"versioned_ensembl_gene_id":"ENSG00000206769.1","gene_symbol":"RNU6-116P","gene_name":"RNA, U6 small nuclear 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:47079]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480553","summary":null,"start":61391595,"end":61391703,"strand":1,"description":"RNA, U6 small nuclear 116, pseudogene [Source:HGNC Symbol;Acc:HGNC:47079]"}, {"versioned_ensembl_gene_id":"ENSG00000200898.1","gene_symbol":"RNU6-1243P","gene_name":"RNA, U6 small nuclear 1243, pseudogene [Source:HGNC Symbol;Acc:HGNC:48206]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481573","summary":null,"start":61937894,"end":61938000,"strand":1,"description":"RNA, U6 small nuclear 1243, pseudogene [Source:HGNC Symbol;Acc:HGNC:48206]"}, {"versioned_ensembl_gene_id":"ENSG00000252050.1","gene_symbol":"SNORA31","gene_name":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]","synonyms":"SNORA31A,ACA31","biotype":"snoRNA","ncbi_id":"677814","summary":null,"start":38308112,"end":38308241,"strand":-1,"description":"Small nucleolar RNA SNORA31 [Source:RFAM;Acc:RF00322]"}, {"versioned_ensembl_gene_id":"ENSG00000199404.1","gene_symbol":"RNA5SP250","gene_name":"RNA, 5S ribosomal pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:43150]","synonyms":"RN5S250","biotype":"rRNA","ncbi_id":"100873506","summary":null,"start":152592973,"end":152593091,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 250 [Source:HGNC Symbol;Acc:HGNC:43150]"}, {"versioned_ensembl_gene_id":"ENSG00000241791.3","gene_symbol":"RN7SL817P","gene_name":"RNA, 7SL, cytoplasmic 817, pseudogene [Source:HGNC Symbol;Acc:HGNC:46833]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481144","summary":null,"start":46448224,"end":46448511,"strand":-1,"description":"RNA, 7SL, cytoplasmic 817, pseudogene [Source:HGNC Symbol;Acc:HGNC:46833]"}, {"versioned_ensembl_gene_id":"ENSG00000200036.1","gene_symbol":"RNA5SP65","gene_name":"RNA, 5S ribosomal pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:42842]","synonyms":"RN5S65","biotype":"rRNA","ncbi_id":"100873300","summary":null,"start":167005959,"end":167006077,"strand":1,"description":"RNA, 5S ribosomal pseudogene 65 [Source:HGNC Symbol;Acc:HGNC:42842]"}, {"versioned_ensembl_gene_id":"ENSG00000252323.1","gene_symbol":"RNU6-184P","gene_name":"RNA, U6 small nuclear 184, pseudogene [Source:HGNC Symbol;Acc:HGNC:47147]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479648","summary":null,"start":16336283,"end":16336389,"strand":-1,"description":"RNA, U6 small nuclear 184, pseudogene [Source:HGNC Symbol;Acc:HGNC:47147]"}, {"versioned_ensembl_gene_id":"ENSG00000251864.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":36672838,"end":36672944,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000201217.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":152449272,"end":152449384,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000278020.1","gene_symbol":"HOXA11-AS1_6","gene_name":"HOXA11 antisense RNA 1 conserved region 6 [Source:RFAM;Acc:RF02142]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":27188816,"end":27188994,"strand":1,"description":"HOXA11 antisense RNA 1 conserved region 6 [Source:RFAM;Acc:RF02142]"}, {"versioned_ensembl_gene_id":"ENSG00000201766.1","gene_symbol":"RNA5SP302","gene_name":"RNA, 5S ribosomal pseudogene 302 [Source:HGNC Symbol;Acc:HGNC:43202]","synonyms":"RN5S302","biotype":"rRNA","ncbi_id":"106479004","summary":null,"start":14663395,"end":14663494,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 302 [Source:HGNC Symbol;Acc:HGNC:43202]"}, {"versioned_ensembl_gene_id":"ENSG00000200220.1","gene_symbol":"RNU6-179P","gene_name":"RNA, U6 small nuclear 179, pseudogene [Source:HGNC Symbol;Acc:HGNC:47142]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479646","summary":null,"start":154039916,"end":154040022,"strand":-1,"description":"RNA, U6 small nuclear 179, pseudogene [Source:HGNC Symbol;Acc:HGNC:47142]"}, {"versioned_ensembl_gene_id":"ENSG00000262477.1","gene_symbol":"AC021224.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32412182,"end":32413236,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280669.1","gene_symbol":"RN7SL32P","gene_name":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480930","summary":null,"start":233205199,"end":233205479,"strand":1,"description":"RNA, 7SL, cytoplasmic 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:46048]"}, {"versioned_ensembl_gene_id":"ENSG00000281309.1","gene_symbol":"SURF6","gene_name":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]","synonyms":"RRP14,FLJ30322","biotype":"protein_coding","ncbi_id":"6838","summary":"This gene encodes a conserved protein that is localized to the nucleolus. The encoded protein may function as a nucleolar-matrix protein with nucleic acid-binding properties. There is a pseudogene for this gene on chromosome Y. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133328922,"end":133336546,"strand":-1,"description":"surfeit 6 [Source:HGNC Symbol;Acc:HGNC:11478]"}, {"versioned_ensembl_gene_id":"ENSG00000280949.1","gene_symbol":"PADI6","gene_name":"peptidyl arginine deiminase 6 [Source:HGNC Symbol;Acc:HGNC:20449]","synonyms":null,"biotype":"protein_coding","ncbi_id":"353238","summary":"This gene encodes a member of the peptidyl arginine deiminase family of enzymes, which catalyze the post-translational deimination of proteins by converting arginine residues into citrullines in the presence of calcium ions. The family members have distinct substrate specificities and tissue-specific expression patterns. This protein may play a role in cytoskeletal reorganization in the egg and in early embryo development. [provided by RefSeq, Sep 2012]","start":17374905,"end":17404408,"strand":1,"description":"peptidyl arginine deiminase 6 [Source:HGNC Symbol;Acc:HGNC:20449]"}, {"versioned_ensembl_gene_id":"ENSG00000281022.2","gene_symbol":"MED22","gene_name":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]","synonyms":"Med24,SURF5,SRB6","biotype":"protein_coding","ncbi_id":"6837","summary":"This gene encodes a protein component of the mediator complex, which functions in the regulation of transcription by bridging interactions between gene-specific regulatory factors, RNA polymerase II, and general transcription factors. Alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2013]","start":133338471,"end":133348279,"strand":-1,"description":"mediator complex subunit 22 [Source:HGNC Symbol;Acc:HGNC:11477]"}, {"versioned_ensembl_gene_id":"ENSG00000281391.1","gene_symbol":"AC004824.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":17409469,"end":17410091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281499.1","gene_symbol":"RNU5A-8P","gene_name":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]","synonyms":null,"biotype":"snRNA","ncbi_id":"100873838","summary":null,"start":210374154,"end":210374267,"strand":-1,"description":"RNA, U5A small nuclear 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:42530]"}, {"versioned_ensembl_gene_id":"ENSG00000280937.1","gene_symbol":"AL034351.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":210462345,"end":210463012,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281540.2","gene_symbol":"RCC2","gene_name":"regulator of chromosome condensation 2 [Source:HGNC Symbol;Acc:HGNC:30297]","synonyms":"TD-60","biotype":"protein_coding","ncbi_id":"55920","summary":"The protein encoded by this gene is a guanine exchange factor that is active on RalA, a small GTPase. The encoded protein and RalA are both essential for proper kinetochore-microtubule function in early mitosis. This protein has been shown to be a biomarker for colorectal cancer. [provided by RefSeq, Oct 2016]","start":17409469,"end":17442433,"strand":-1,"description":"regulator of chromosome condensation 2 [Source:HGNC Symbol;Acc:HGNC:30297]"}, {"versioned_ensembl_gene_id":"ENSG00000281456.1","gene_symbol":"AC099669.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44557357,"end":44685653,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280661.2","gene_symbol":"ZNF660","gene_name":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]","synonyms":"FLJ36870","biotype":"protein_coding","ncbi_id":"285349","summary":"This gene encodes a protein that contains multiple C2H2 zinc finger domains, and is located in a cluster of zinc-finger encoding genes on chromosome 3. Naturally-occurring readthrough transcription is observed between this gene and the downstream zinc finger protein 197 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017]","start":44578223,"end":44599694,"strand":1,"description":"zinc finger protein 660 [Source:HGNC Symbol;Acc:HGNC:26720]"}, {"versioned_ensembl_gene_id":"ENSG00000280795.1","gene_symbol":"MPRIPP1","gene_name":"myosin phosphatase Rho interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44594]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421374","summary":null,"start":44579938,"end":44581026,"strand":-1,"description":"myosin phosphatase Rho interacting protein pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44594]"}, {"versioned_ensembl_gene_id":"ENSG00000283965.1","gene_symbol":"KCNH1","gene_name":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]","synonyms":"Kv10.1,h-eag,eag1,eag","biotype":"protein_coding","ncbi_id":"3756","summary":"Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit of a voltage-gated non-inactivating delayed rectifier potassium channel. It is activated at the onset of myoblast differentiation. The gene is highly expressed in brain and in myoblasts. Overexpression of the gene may confer a growth advantage to cancer cells and favor tumor cell proliferation. Alternative splicing of this gene results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]","start":210680180,"end":211137537,"strand":-1,"description":"potassium voltage-gated channel subfamily H member 1 [Source:HGNC Symbol;Acc:HGNC:6250]"}, {"versioned_ensembl_gene_id":"ENSG00000281709.2","gene_symbol":"ZNF197","gene_name":"zinc finger protein 197 [Source:HGNC Symbol;Acc:HGNC:12988]","synonyms":"D3S1363E,ZSCAN41,ZNF166,ZKSCAN9,P18","biotype":"protein_coding","ncbi_id":"10168","summary":"This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein contains 20 tandemly arrayed C2H2-type zinc fingers, a Kruppel-associated box (KRAB) domain, and a SCAN box. This transcript turns over rapidly and contains 3' UTR AUUUA motifs, which are often a hallmark of rapid turnover. It is overexpressed in some thyroid papillary carcinomas. This gene is located in a cluster of zinc finger genes at 3p21. Naturally-occurring readthrough transcription is observed between this gene and the upstream zinc finger protein 660 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017]","start":44584888,"end":44648471,"strand":1,"description":"zinc finger protein 197 [Source:HGNC Symbol;Acc:HGNC:12988]"}, {"versioned_ensembl_gene_id":"ENSG00000281699.1","gene_symbol":"AL772161.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":133339138,"end":133339613,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280948.1","gene_symbol":"MIR1976","gene_name":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]","synonyms":"hsa-mir-1976","biotype":"miRNA","ncbi_id":"100302190","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":26554542,"end":26554593,"strand":1,"description":"microRNA 1976 [Source:HGNC Symbol;Acc:HGNC:37064]"}, {"versioned_ensembl_gene_id":"ENSG00000281092.1","gene_symbol":"RN7SL679P","gene_name":"RNA, 7SL, cytoplasmic 679, pseudogene [Source:HGNC Symbol;Acc:HGNC:46695]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106481855","summary":null,"start":26593243,"end":26593546,"strand":-1,"description":"RNA, 7SL, cytoplasmic 679, pseudogene [Source:HGNC Symbol;Acc:HGNC:46695]"}, {"versioned_ensembl_gene_id":"ENSG00000280876.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":26593940,"end":26594041,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000281679.1","gene_symbol":"RNU7-29P","gene_name":"RNA, U7 small nuclear 29 pseudogene [Source:HGNC Symbol;Acc:HGNC:34125]","synonyms":"U7.29","biotype":"snRNA","ncbi_id":"100147816","summary":null,"start":26602369,"end":26602432,"strand":-1,"description":"RNA, U7 small nuclear 29 pseudogene [Source:HGNC Symbol;Acc:HGNC:34125]"}, {"versioned_ensembl_gene_id":"ENSG00000280806.1","gene_symbol":"AL627313.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":26640377,"end":26640614,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280926.1","gene_symbol":"snoU13","gene_name":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":26645671,"end":26645774,"strand":1,"description":"Small nucleolar RNA U13 [Source:RFAM;Acc:RF01210]"}, {"versioned_ensembl_gene_id":"ENSG00000280858.2","gene_symbol":"RPL7A","gene_name":"ribosomal protein L7a [Source:HGNC Symbol;Acc:HGNC:10364]","synonyms":"TRUP,SURF3,L7A","biotype":"protein_coding","ncbi_id":"6130","summary":"Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L7AE family of ribosomal proteins. It can interact with a subclass of nuclear hormone receptors, including thyroid hormone receptor, and inhibit their ability to transactivate by preventing their binding to their DNA response elements. This gene is included in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity. It is co-transcribed with the U24, U36a, U36b, and U36c small nucleolar RNA genes, which are located in its second, fifth, fourth, and sixth introns, respectively. This gene rearranges with the trk proto-oncogene to form the chimeric oncogene trk-2h, which encodes an oncoprotein consisting of the N terminus of ribosomal protein L7a fused to the receptor tyrosine kinase domain of trk. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":133348362,"end":133351574,"strand":1,"description":"ribosomal protein L7a [Source:HGNC Symbol;Acc:HGNC:10364]"}, {"versioned_ensembl_gene_id":"ENSG00000280907.1","gene_symbol":"ZNF197-AS1","gene_name":"ZNF197 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40620]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874094","summary":null,"start":44617128,"end":44624797,"strand":-1,"description":"ZNF197 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40620]"}, {"versioned_ensembl_gene_id":"ENSG00000281306.2","gene_symbol":"ZNF35","gene_name":"zinc finger protein 35 [Source:HGNC Symbol;Acc:HGNC:13099]","synonyms":"Zfp105,HF10,HF.10","biotype":"protein_coding","ncbi_id":"7584","summary":null,"start":44648727,"end":44660791,"strand":1,"description":"zinc finger protein 35 [Source:HGNC Symbol;Acc:HGNC:13099]"}, {"versioned_ensembl_gene_id":"ENSG00000281102.1","gene_symbol":"AC092046.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":44667412,"end":44669364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280872.1","gene_symbol":"SOCS5P3","gene_name":"suppressor of cytokine signaling 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44599]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100127945","summary":null,"start":44709307,"end":44710882,"strand":-1,"description":"suppressor of cytokine signaling 5 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44599]"}, {"versioned_ensembl_gene_id":"ENSG00000281448.2","gene_symbol":"ZNF502","gene_name":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]","synonyms":"FLJ14855,FLJ12515","biotype":"protein_coding","ncbi_id":"91392","summary":null,"start":44712639,"end":44723827,"strand":1,"description":"zinc finger protein 502 [Source:HGNC Symbol;Acc:HGNC:23718]"}, {"versioned_ensembl_gene_id":"ENSG00000280889.1","gene_symbol":"SNORD24","gene_name":"small nucleolar RNA, C/D box 24 [Source:HGNC Symbol;Acc:HGNC:10146]","synonyms":"U24,RNU24","biotype":"snoRNA","ncbi_id":"26820","summary":null,"start":133349544,"end":133349618,"strand":1,"description":"small nucleolar RNA, C/D box 24 [Source:HGNC Symbol;Acc:HGNC:10146]"}, {"versioned_ensembl_gene_id":"ENSG00000281243.1","gene_symbol":"SNORD36B","gene_name":"small nucleolar RNA, C/D box 36B [Source:HGNC Symbol;Acc:HGNC:10164]","synonyms":"U36b,RNU36B","biotype":"snoRNA","ncbi_id":"26814","summary":null,"start":133350243,"end":133350316,"strand":1,"description":"small nucleolar RNA, C/D box 36B [Source:HGNC Symbol;Acc:HGNC:10164]"}, {"versioned_ensembl_gene_id":"ENSG00000281907.1","gene_symbol":"SNORD36A","gene_name":"small nucleolar RNA, C/D box 36A [Source:HGNC Symbol;Acc:HGNC:10163]","synonyms":"U36a,RNU36A","biotype":"snoRNA","ncbi_id":"26815","summary":null,"start":133350604,"end":133350676,"strand":1,"description":"small nucleolar RNA, C/D box 36A [Source:HGNC Symbol;Acc:HGNC:10163]"}, {"versioned_ensembl_gene_id":"ENSG00000281541.1","gene_symbol":"SNORD36C","gene_name":"small nucleolar RNA, C/D box 36C [Source:HGNC Symbol;Acc:HGNC:10165]","synonyms":"U36c,RNU36C","biotype":"snoRNA","ncbi_id":"26813","summary":null,"start":133350995,"end":133351060,"strand":1,"description":"small nucleolar RNA, C/D box 36C [Source:HGNC Symbol;Acc:HGNC:10165]"}, {"versioned_ensembl_gene_id":"ENSG00000280627.2","gene_symbol":"SURF1","gene_name":"SURF1, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:11474]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6834","summary":"This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. [provided by RefSeq, Jul 2008]","start":133351903,"end":133356824,"strand":-1,"description":"SURF1, cytochrome c oxidase assembly factor [Source:HGNC Symbol;Acc:HGNC:11474]"}, {"versioned_ensembl_gene_id":"ENSG00000281089.2","gene_symbol":"ATG16L1","gene_name":"autophagy related 16 like 1 [Source:HGNC Symbol;Acc:HGNC:21498]","synonyms":"WDR30,FLJ10035,ATG16L,ATG16A,APG16L","biotype":"protein_coding","ncbi_id":"55054","summary":"The protein encoded by this gene is part of a large protein complex that is necessary for autophagy, the major process by which intracellular components are targeted to lysosomes for degradation. Defects in this gene are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]","start":233210051,"end":233295674,"strand":1,"description":"autophagy related 16 like 1 [Source:HGNC Symbol;Acc:HGNC:21498]"}, {"versioned_ensembl_gene_id":"ENSG00000281661.2","gene_symbol":"ZNF501","gene_name":"zinc finger protein 501 [Source:HGNC Symbol;Acc:HGNC:23717]","synonyms":"ZNF52,MGC21738","biotype":"protein_coding","ncbi_id":"115560","summary":null,"start":44729592,"end":44737079,"strand":1,"description":"zinc finger protein 501 [Source:HGNC Symbol;Acc:HGNC:23717]"}, {"versioned_ensembl_gene_id":"ENSG00000281665.1","gene_symbol":"KIAA1143","gene_name":"KIAA1143 [Source:HGNC Symbol;Acc:HGNC:29198]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57456","summary":null,"start":44737657,"end":44761658,"strand":-1,"description":"KIAA1143 [Source:HGNC Symbol;Acc:HGNC:29198]"}, {"versioned_ensembl_gene_id":"ENSG00000281024.2","gene_symbol":"SURF2","gene_name":"surfeit 2 [Source:HGNC Symbol;Acc:HGNC:11475]","synonyms":null,"biotype":"protein_coding","ncbi_id":"6835","summary":"This gene shares a bidirectional promoter with surfeit 1 (SURF1; GeneID: 6834), which is located on the opposite strand. It encodes a conserved protein that is expressed in a variety of tissues. [provided by RefSeq, Jul 2013]","start":133356700,"end":133361317,"strand":1,"description":"surfeit 2 [Source:HGNC Symbol;Acc:HGNC:11475]"}, {"versioned_ensembl_gene_id":"ENSG00000280610.2","gene_symbol":"KIF15","gene_name":"kinesin family member 15 [Source:HGNC Symbol;Acc:HGNC:17273]","synonyms":"NY-BR-62,KNSL7,HKLP2","biotype":"protein_coding","ncbi_id":"56992","summary":null,"start":44761713,"end":44873372,"strand":1,"description":"kinesin family member 15 [Source:HGNC Symbol;Acc:HGNC:17273]"}, {"versioned_ensembl_gene_id":"ENSG00000280951.2","gene_symbol":"SURF4","gene_name":"surfeit 4 [Source:HGNC Symbol;Acc:HGNC:11476]","synonyms":"MGC102753,FLJ22993,ERV29","biotype":"protein_coding","ncbi_id":"6836","summary":"This gene is located in the surfeit gene cluster, which is comprised of very tightly linked housekeeping genes that do not share sequence similarity. The encoded protein is a conserved integral membrane protein that interacts with endoplasmic reticulum-Golgi intermediate compartment proteins. Disruption of this gene results in reduced numbers of endoplasmic reticulum-Golgi intermediate compartment clusters and redistribution of coat protein I to the cytosol. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133361597,"end":133376314,"strand":-1,"description":"surfeit 4 [Source:HGNC Symbol;Acc:HGNC:11476]"}, {"versioned_ensembl_gene_id":"ENSG00000281245.1","gene_symbol":"STKLD1","gene_name":"serine/threonine kinase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28669]","synonyms":"MGC43306,C9orf96,SGK071","biotype":"protein_coding","ncbi_id":"169436","summary":null,"start":133376515,"end":133406244,"strand":1,"description":"serine/threonine kinase like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28669]"}, {"versioned_ensembl_gene_id":"ENSG00000280516.3","gene_symbol":"TMEM42","gene_name":"transmembrane protein 42 [Source:HGNC Symbol;Acc:HGNC:28444]","synonyms":"MGC29956","biotype":"protein_coding","ncbi_id":"131616","summary":null,"start":44861865,"end":44865666,"strand":1,"description":"transmembrane protein 42 [Source:HGNC Symbol;Acc:HGNC:28444]"}, {"versioned_ensembl_gene_id":"ENSG00000282258.1","gene_symbol":"PRAMEF34P","gene_name":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"649324","summary":null,"start":13068006,"end":13070798,"strand":-1,"description":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]"}, {"versioned_ensembl_gene_id":"ENSG00000282562.1","gene_symbol":"PRAMEF35P","gene_name":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419649","summary":null,"start":13077230,"end":13078516,"strand":-1,"description":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]"}, {"versioned_ensembl_gene_id":"ENSG00000284275.1","gene_symbol":"MIR564","gene_name":"microRNA 564 [Source:HGNC Symbol;Acc:HGNC:32820]","synonyms":"MIRN564,hsa-mir-564","biotype":"miRNA","ncbi_id":"693149","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":44861884,"end":44861977,"strand":1,"description":"microRNA 564 [Source:HGNC Symbol;Acc:HGNC:32820]"}, {"versioned_ensembl_gene_id":"ENSG00000281886.2","gene_symbol":"TGM4","gene_name":"transglutaminase 4 [Source:HGNC Symbol;Acc:HGNC:11780]","synonyms":"TGP","biotype":"protein_coding","ncbi_id":"7047","summary":null,"start":44874604,"end":44914986,"strand":1,"description":"transglutaminase 4 [Source:HGNC Symbol;Acc:HGNC:11780]"}, {"versioned_ensembl_gene_id":"ENSG00000280706.2","gene_symbol":"REXO4","gene_name":"REX4 homolog, 3'-5' exonuclease [Source:HGNC Symbol;Acc:HGNC:12820]","synonyms":"XPMC2H,hPMC2","biotype":"protein_coding","ncbi_id":"57109","summary":null,"start":133406207,"end":133418244,"strand":-1,"description":"REX4 homolog, 3'-5' exonuclease [Source:HGNC Symbol;Acc:HGNC:12820]"}, {"versioned_ensembl_gene_id":"ENSG00000280701.1","gene_symbol":"AC098649.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":44899174,"end":44900921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280674.2","gene_symbol":"ZDHHC3","gene_name":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]","synonyms":"ZNF373,GODZ,DHHC3","biotype":"protein_coding","ncbi_id":"51304","summary":null,"start":44915253,"end":44976181,"strand":-1,"description":"zinc finger DHHC-type containing 3 [Source:HGNC Symbol;Acc:HGNC:18470]"}, {"versioned_ensembl_gene_id":"ENSG00000280652.1","gene_symbol":"SCARNA5","gene_name":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]","synonyms":"U87","biotype":"scaRNA","ncbi_id":"677775","summary":null,"start":233275727,"end":233276002,"strand":1,"description":"small Cajal body-specific RNA 5 [Source:HGNC Symbol;Acc:HGNC:32561]"}, {"versioned_ensembl_gene_id":"ENSG00000281388.1","gene_symbol":"SCARNA6","gene_name":"small Cajal body-specific RNA 6 [Source:HGNC Symbol;Acc:HGNC:32562]","synonyms":"U88","biotype":"scaRNA","ncbi_id":"677772","summary":null,"start":233288676,"end":233288940,"strand":1,"description":"small Cajal body-specific RNA 6 [Source:HGNC Symbol;Acc:HGNC:32562]"}, {"versioned_ensembl_gene_id":"ENSG00000281857.2","gene_symbol":"SAG","gene_name":"S-antigen visual arrestin [Source:HGNC Symbol;Acc:HGNC:10521]","synonyms":"RP47,ARRESTIN","biotype":"protein_coding","ncbi_id":"6295","summary":"Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness. [provided by RefSeq, Jul 2008]","start":233307816,"end":233347055,"strand":1,"description":"S-antigen visual arrestin [Source:HGNC Symbol;Acc:HGNC:10521]"}, {"versioned_ensembl_gene_id":"ENSG00000280928.1","gene_symbol":"AC013726.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":233351132,"end":233353416,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280873.3","gene_symbol":"DGKD","gene_name":"diacylglycerol kinase delta [Source:HGNC Symbol;Acc:HGNC:2851]","synonyms":"KIAA0145,DGKdelta","biotype":"protein_coding","ncbi_id":"8527","summary":"This gene encodes a cytoplasmic enzyme that phosphorylates diacylglycerol to produce phosphatidic acid. Diacylglycerol and phosphatidic acid are two lipids that act as second messengers in signaling cascades. Their cellular concentrations are regulated by the encoded protein, and so it is thought to play an important role in cellular signal transduction. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]","start":233354507,"end":233472104,"strand":1,"description":"diacylglycerol kinase delta [Source:HGNC Symbol;Acc:HGNC:2851]"}, {"versioned_ensembl_gene_id":"ENSG00000281244.2","gene_symbol":"ADAMTS13","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]","synonyms":"FLJ42993,VWFCP,DKFZp434C2322,vWF-CP,C9orf8,TTP,MGC118900,MGC118899","biotype":"protein_coding","ncbi_id":"11093","summary":"This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":133414506,"end":133459550,"strand":1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]"}, {"versioned_ensembl_gene_id":"ENSG00000281623.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":233379843,"end":233379955,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000280479.2","gene_symbol":"CACFD1","gene_name":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]","synonyms":"flower,D9S2135,C9orf7","biotype":"protein_coding","ncbi_id":"11094","summary":null,"start":133460113,"end":133470996,"strand":1,"description":"calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]"}, {"versioned_ensembl_gene_id":"ENSG00000281879.2","gene_symbol":"ABO","gene_name":"ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase [Source:HGNC Symbol;Acc:HGNC:79]","synonyms":"A3GALT1,A3GALNT","biotype":"protein_coding","ncbi_id":"28","summary":"This gene encodes proteins related to the first discovered blood group system, ABO. Variation in the ABO gene (chromosome 9q34.2) is the basis of the ABO blood group, thus the presence of an allele determines the blood group in an individual. The 'O' blood group is caused by a deletion of guanine-258 near the N-terminus of the protein which results in a frameshift and translation of an almost entirely different protein. Individuals with the A, B, and AB alleles express glycosyltransferase activities that convert the H antigen into the A or B antigen. Other minor alleles have been found for this gene. This locus has been identified as a susceptibility locus for severe coronavirus disease 2019 (COVID-19) by genome-wide association study. [provided by RefSeq, Aug 2020]","start":133255752,"end":133275337,"strand":-1,"description":"ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase [Source:HGNC Symbol;Acc:HGNC:79]"}, {"versioned_ensembl_gene_id":"ENSG00000283984.1","gene_symbol":"AL593848.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":133350829,"end":133351541,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283909.1","gene_symbol":"AL593848.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":133391462,"end":133391838,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282873.1","gene_symbol":"BCL7A","gene_name":"BCL tumor suppressor 7A [Source:HGNC Symbol;Acc:HGNC:1004]","synonyms":"BCL7","biotype":"protein_coding","ncbi_id":"605","summary":"This gene is directly involved, with Myc and IgH, in a three-way gene translocation in a Burkitt lymphoma cell line. As a result of the gene translocation, the N-terminal region of the gene product is disrupted, which is thought to be related to the pathogenesis of a subset of high-grade B cell non-Hodgkin lymphoma. The N-terminal segment involved in the translocation includes the region that shares a strong sequence similarity with those of BCL7B and BCL7C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":122019422,"end":122062044,"strand":1,"description":"BCL tumor suppressor 7A [Source:HGNC Symbol;Acc:HGNC:1004]"}, {"versioned_ensembl_gene_id":"ENSG00000281211.1","gene_symbol":"CTBP2P1","gene_name":"C-terminal binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"352905","summary":null,"start":56890001,"end":56890245,"strand":1,"description":"C-terminal binding protein 2 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:23940]"}, {"versioned_ensembl_gene_id":"ENSG00000282530.1","gene_symbol":"HNRNPCL2","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]","synonyms":"HNRNPCP5,HNRNPCP5","biotype":"protein_coding","ncbi_id":"440563","summary":null,"start":13088323,"end":13089681,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]"}, {"versioned_ensembl_gene_id":"ENSG00000281277.3","gene_symbol":"FOXR1","gene_name":"forkhead box R1 [Source:HGNC Symbol;Acc:HGNC:29980]","synonyms":"DLNB13,FOXN5","biotype":"protein_coding","ncbi_id":"283150","summary":"This gene encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix-turn-helix proteins with a core DNA-binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. This forkhead box protein lacks the C-terminal basic region found in many other FOX family members. It is located within the 11q23.3 region which is commonly deleted in neuroblastomas. [provided by RefSeq, Jul 2008]","start":118971707,"end":118981291,"strand":1,"description":"forkhead box R1 [Source:HGNC Symbol;Acc:HGNC:29980]"}, {"versioned_ensembl_gene_id":"ENSG00000283035.1","gene_symbol":"NALCN-AS1","gene_name":"NALCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42743]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100885778","summary":null,"start":100708325,"end":101059169,"strand":1,"description":"NALCN antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:42743]"}, {"versioned_ensembl_gene_id":"ENSG00000283302.1","gene_symbol":"FP565324.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":113953705,"end":113973998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281256.1","gene_symbol":"AL360225.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":74823667,"end":74824187,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281865.1","gene_symbol":"LINC00411","gene_name":"long intergenic non-protein coding RNA 411 [Source:HGNC Symbol;Acc:HGNC:42744]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100874161","summary":null,"start":100940862,"end":100944364,"strand":-1,"description":"long intergenic non-protein coding RNA 411 [Source:HGNC Symbol;Acc:HGNC:42744]"}, {"versioned_ensembl_gene_id":"ENSG00000284223.1","gene_symbol":"AC255545.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":17769922,"end":17771135,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281509.1","gene_symbol":"AL356585.7","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18343918,"end":18348373,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280651.1","gene_symbol":"AC156455.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":122063306,"end":122068616,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281252.1","gene_symbol":"FAM230C","gene_name":"family with sequence similarity 230 member C [Source:HGNC Symbol;Acc:HGNC:24482]","synonyms":"NCRNA00281,LINC00281,DKFZP434B061","biotype":"processed_transcript","ncbi_id":"26080","summary":null,"start":18365205,"end":18401932,"strand":1,"description":"family with sequence similarity 230 member C [Source:HGNC Symbol;Acc:HGNC:24482]"}, {"versioned_ensembl_gene_id":"ENSG00000281029.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":118994334,"end":118994630,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000283318.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":118994560,"end":118994655,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000282162.1","gene_symbol":"LINC01784","gene_name":"long intergenic non-protein coding RNA 1784 [Source:HGNC Symbol;Acc:HGNC:52574]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105376745","summary":null,"start":12822686,"end":12823159,"strand":-1,"description":"long intergenic non-protein coding RNA 1784 [Source:HGNC Symbol;Acc:HGNC:52574]"}, {"versioned_ensembl_gene_id":"ENSG00000281705.1","gene_symbol":"AP003392.11","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":118994824,"end":118998004,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281175.2","gene_symbol":"AL356585.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18376478,"end":18377374,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284712.1","gene_symbol":"AL356585.11","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18418821,"end":18418943,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280774.2","gene_symbol":"LEUTX","gene_name":"leucine twenty homeobox [Source:HGNC Symbol;Acc:HGNC:31953]","synonyms":null,"biotype":"protein_coding","ncbi_id":"342900","summary":null,"start":39776595,"end":39786167,"strand":1,"description":"leucine twenty homeobox [Source:HGNC Symbol;Acc:HGNC:31953]"}, {"versioned_ensembl_gene_id":"ENSG00000281616.1","gene_symbol":"GGT4P","gene_name":"gamma-glutamyltransferase 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33207]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"643171","summary":null,"start":18423434,"end":18440730,"strand":-1,"description":"gamma-glutamyltransferase 4 pseudogene [Source:HGNC Symbol;Acc:HGNC:33207]"}, {"versioned_ensembl_gene_id":"ENSG00000281934.1","gene_symbol":"PRAMEF11","gene_name":"PRAME family member 11 [Source:HGNC Symbol;Acc:HGNC:14086]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440560","summary":null,"start":12824605,"end":12831410,"strand":-1,"description":"PRAME family member 11 [Source:HGNC Symbol;Acc:HGNC:14086]"}, {"versioned_ensembl_gene_id":"ENSG00000280477.1","gene_symbol":"RASA3","gene_name":"RAS p21 protein activator 3 [Source:HGNC Symbol;Acc:HGNC:20331]","synonyms":"GAPIII,GAP1IP4BP","biotype":"protein_coding","ncbi_id":"22821","summary":"This gene encodes a protein that binds inositol 1,3,4,5-tetrakisphosphate and stimulates the GTPase activity of Ras p21. This protein functions as a negative regulator of the Ras signalling pathway. It is localized to the cell membrane via a pleckstrin homology (PH) domain in the C-terminal region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]","start":113977784,"end":114128677,"strand":-1,"description":"RAS p21 protein activator 3 [Source:HGNC Symbol;Acc:HGNC:20331]"}, {"versioned_ensembl_gene_id":"ENSG00000281084.1","gene_symbol":"AL356585.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18449228,"end":18479842,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281677.1","gene_symbol":"AC005393.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":39812972,"end":39813555,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280895.2","gene_symbol":"SETD8P1","gene_name":"SET domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30088]","synonyms":"SET07p","biotype":"processed_pseudogene","ncbi_id":"57108","summary":null,"start":18467462,"end":18468641,"strand":1,"description":"SET domain containing 8 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:30088]"}, {"versioned_ensembl_gene_id":"ENSG00000281878.1","gene_symbol":"AL356585.8","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18501841,"end":18518504,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281449.2","gene_symbol":"BCL2L14","gene_name":"BCL2 like 14 [Source:HGNC Symbol;Acc:HGNC:16657]","synonyms":"BCLG,BCL-G","biotype":"protein_coding","ncbi_id":"79370","summary":"The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. Overexpression of this gene has been shown to induce apoptosis in cells. Three alternatively spliced transcript variants encoding two distinct isoforms have been reported for this gene. [provided by RefSeq, May 2009]","start":12049844,"end":12211084,"strand":1,"description":"BCL2 like 14 [Source:HGNC Symbol;Acc:HGNC:16657]"}, {"versioned_ensembl_gene_id":"ENSG00000284573.1","gene_symbol":"BAGE3","gene_name":"BAGE family member 3 [Source:NCBI gene;Acc:85318]","synonyms":"CT2.3","biotype":"protein_coding","ncbi_id":"85318","summary":null,"start":18249130,"end":18312664,"strand":1,"description":"BAGE family member 3 [Source:NCBI gene;Acc:85318]"}, {"versioned_ensembl_gene_id":"ENSG00000280975.2","gene_symbol":"CCDC84","gene_name":"coiled-coil domain containing 84 [Source:HGNC Symbol;Acc:HGNC:30460]","synonyms":"DLNB14","biotype":"protein_coding","ncbi_id":"338657","summary":"This gene encodes a protein thought to contain a coiled coil motif. No function has been determined for the encoded protein. A pseudogene of this gene is located on chromosome 20. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]","start":118998142,"end":119015791,"strand":1,"description":"coiled-coil domain containing 84 [Source:HGNC Symbol;Acc:HGNC:30460]"}, {"versioned_ensembl_gene_id":"ENSG00000283864.1","gene_symbol":"AL356585.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18405408,"end":18407072,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282116.1","gene_symbol":"PRAMEF30P","gene_name":"PRAME family member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:51892]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"441870","summary":null,"start":12838125,"end":12841357,"strand":-1,"description":"PRAME family member 30, pseudogene [Source:HGNC Symbol;Acc:HGNC:51892]"}, {"versioned_ensembl_gene_id":"ENSG00000281178.2","gene_symbol":"MLXIP","gene_name":"MLX interacting protein [Source:HGNC Symbol;Acc:HGNC:17055]","synonyms":"bHLHe36,MONDOA,MIR,KIAA0867","biotype":"protein_coding","ncbi_id":"22877","summary":"This gene encodes a protein that functions as part of a heterodimer to activate transcription. The encoded protein forms a heterodimer with Max-like protein X (MLX) and is involved in the regulation of genes in response to cellular glucose levels. [provided by RefSeq, Mar 2014]","start":122078722,"end":122146038,"strand":1,"description":"MLX interacting protein [Source:HGNC Symbol;Acc:HGNC:17055]"}, {"versioned_ensembl_gene_id":"ENSG00000282175.2","gene_symbol":"HNRNPCL1","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:HGNC:29295]","synonyms":"HNRPCL1","biotype":"protein_coding","ncbi_id":"343069","summary":null,"start":12847408,"end":12848725,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:HGNC:29295]"}, {"versioned_ensembl_gene_id":"ENSG00000282468.1","gene_symbol":"PRAMEF36P","gene_name":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645354","summary":null,"start":13101645,"end":13104442,"strand":1,"description":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]"}, {"versioned_ensembl_gene_id":"ENSG00000282310.1","gene_symbol":"IGKV3-7","gene_name":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28915","summary":null,"start":88978468,"end":88979081,"strand":-1,"description":"immunoglobulin kappa variable 3-7 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5821]"}, {"versioned_ensembl_gene_id":"ENSG00000283113.2","gene_symbol":"IGKV1-8","gene_name":"immunoglobulin kappa variable 1-8 [Source:HGNC Symbol;Acc:HGNC:5743]","synonyms":"L9,IGKV18","biotype":"IG_V_gene","ncbi_id":"28942","summary":null,"start":88992409,"end":88992931,"strand":-1,"description":"immunoglobulin kappa variable 1-8 [Source:HGNC Symbol;Acc:HGNC:5743]"}, {"versioned_ensembl_gene_id":"ENSG00000281813.2","gene_symbol":"KAT6B","gene_name":"lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]","synonyms":"ZC2HC6B,querkopf,qkf,MYST4,MOZ2,Morf","biotype":"protein_coding","ncbi_id":"23522","summary":"The protein encoded by this gene is a histone acetyltransferase and component of the MOZ/MORF protein complex. In addition to its acetyltransferase activity, the encoded protein has transcriptional activation activity in its N-terminal end and transcriptional repression activity in its C-terminal end. This protein is necessary for RUNX2-dependent transcriptional activation and could be involved in brain development. Mutations have been found in patients with genitopatellar syndrome. A translocation of this gene and the CREBBP gene results in acute myeloid leukemias. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]","start":74827639,"end":75034679,"strand":1,"description":"lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]"}, {"versioned_ensembl_gene_id":"ENSG00000282817.1","gene_symbol":"PRAMEF2","gene_name":"PRAME family member 2 [Source:HGNC Symbol;Acc:HGNC:28841]","synonyms":"FLJ43580","biotype":"protein_coding","ncbi_id":"65122","summary":null,"start":12857086,"end":12861909,"strand":1,"description":"PRAME family member 2 [Source:HGNC Symbol;Acc:HGNC:28841]"}, {"versioned_ensembl_gene_id":"ENSG00000281320.2","gene_symbol":"DYRK1B","gene_name":"dual specificity tyrosine phosphorylation regulated kinase 1B [Source:HGNC Symbol;Acc:HGNC:3092]","synonyms":"MIRK","biotype":"protein_coding","ncbi_id":"9149","summary":"This gene encodes a member of a family of nuclear-localized protein kinases. The encoded protein participates in the regulation of the cell cycle. Expression of this gene may be altered in tumor cells, and mutations in this gene were found to cause abdominal obesity-metabolic syndrome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]","start":39825350,"end":39834201,"strand":-1,"description":"dual specificity tyrosine phosphorylation regulated kinase 1B [Source:HGNC Symbol;Acc:HGNC:3092]"}, {"versioned_ensembl_gene_id":"ENSG00000282584.1","gene_symbol":"PRAMEF4","gene_name":"PRAME family member 4 [Source:HGNC Symbol;Acc:HGNC:31971]","synonyms":"RP5-845O24.6","biotype":"protein_coding","ncbi_id":"400735","summary":null,"start":12879224,"end":12886201,"strand":-1,"description":"PRAME family member 4 [Source:HGNC Symbol;Acc:HGNC:31971]"}, {"versioned_ensembl_gene_id":"ENSG00000282663.1","gene_symbol":"PRAMEF10","gene_name":"PRAME family member 10 [Source:HGNC Symbol;Acc:HGNC:27997]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343071","summary":null,"start":12892896,"end":12898270,"strand":-1,"description":"PRAME family member 10 [Source:HGNC Symbol;Acc:HGNC:27997]"}, {"versioned_ensembl_gene_id":"ENSG00000280531.1","gene_symbol":"RASA3-IT1","gene_name":"RASA3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39938]","synonyms":null,"biotype":"sense_intronic","ncbi_id":"100874321","summary":null,"start":114103635,"end":114104886,"strand":-1,"description":"RASA3 intronic transcript 1 [Source:HGNC Symbol;Acc:HGNC:39938]"}, {"versioned_ensembl_gene_id":"ENSG00000279195.2","gene_symbol":"PRAMEF7","gene_name":"PRAME family member 7 [Source:HGNC Symbol;Acc:HGNC:28415]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441871","summary":null,"start":12916610,"end":12920482,"strand":1,"description":"PRAME family member 7 [Source:HGNC Symbol;Acc:HGNC:28415]"}, {"versioned_ensembl_gene_id":"ENSG00000282338.1","gene_symbol":"RNU6-1072P","gene_name":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480037","summary":null,"start":12922554,"end":12922660,"strand":1,"description":"RNA, U6 small nuclear 1072, pseudogene [Source:HGNC Symbol;Acc:HGNC:48035]"}, {"versioned_ensembl_gene_id":"ENSG00000281913.1","gene_symbol":"RPL23AP64","gene_name":"ribosomal protein L23a pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:36552]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"649946","summary":null,"start":119003012,"end":119003446,"strand":-1,"description":"ribosomal protein L23a pseudogene 64 [Source:HGNC Symbol;Acc:HGNC:36552]"}, {"versioned_ensembl_gene_id":"ENSG00000282549.1","gene_symbol":"PRAMEF29P","gene_name":"PRAME family member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:51891]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"729356","summary":null,"start":12926162,"end":12928253,"strand":1,"description":"PRAME family member 29, pseudogene [Source:HGNC Symbol;Acc:HGNC:51891]"}, {"versioned_ensembl_gene_id":"ENSG00000280582.1","gene_symbol":"AP003392.7","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119003742,"end":119004893,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281697.1","gene_symbol":"AP003392.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":119005727,"end":119005934,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282119.2","gene_symbol":"PRAMEF6","gene_name":"PRAME family member 6 [Source:HGNC Symbol;Acc:HGNC:30583]","synonyms":null,"biotype":"protein_coding","ncbi_id":"440561","summary":null,"start":12938472,"end":12947580,"strand":-1,"description":"PRAME family member 6 [Source:HGNC Symbol;Acc:HGNC:30583]"}, {"versioned_ensembl_gene_id":"ENSG00000280831.2","gene_symbol":"RPS25","gene_name":"ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:10413]","synonyms":"S25","biotype":"protein_coding","ncbi_id":"6230","summary":"Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S25E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]","start":119015712,"end":119018691,"strand":-1,"description":"ribosomal protein S25 [Source:HGNC Symbol;Acc:HGNC:10413]"}, {"versioned_ensembl_gene_id":"ENSG00000281442.1","gene_symbol":"AC007537.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12111163,"end":12111489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283344.1","gene_symbol":"MIR1244-4","gene_name":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]","synonyms":null,"biotype":"miRNA","ncbi_id":"103504734","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":12111952,"end":12112036,"strand":1,"description":"microRNA 1244-4 [Source:HGNC Symbol;Acc:HGNC:50831]"}, {"versioned_ensembl_gene_id":"ENSG00000282791.1","gene_symbol":"PRAMEF28P","gene_name":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]","synonyms":"PRAMEF28","biotype":"unprocessed_pseudogene","ncbi_id":"102724742","summary":null,"start":13002166,"end":13004957,"strand":1,"description":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]"}, {"versioned_ensembl_gene_id":"ENSG00000282437.2","gene_symbol":"PRAMEF27","gene_name":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101929983","summary":null,"start":13022303,"end":13029318,"strand":-1,"description":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]"}, {"versioned_ensembl_gene_id":"ENSG00000282559.1","gene_symbol":"HNRNPCL3","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"649330","summary":null,"start":13033696,"end":13035056,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]"}, {"versioned_ensembl_gene_id":"ENSG00000282566.2","gene_symbol":"PRAMEF25","gene_name":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441873","summary":null,"start":13041504,"end":13050711,"strand":1,"description":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]"}, {"versioned_ensembl_gene_id":"ENSG00000281324.2","gene_symbol":"LRP6","gene_name":"LDL receptor related protein 6 [Source:HGNC Symbol;Acc:HGNC:6698]","synonyms":"ADCAD2","biotype":"protein_coding","ncbi_id":"4040","summary":"This gene encodes a member of the low density lipoprotein (LDL) receptor gene family. LDL receptors are transmembrane cell surface proteins involved in receptor-mediated endocytosis of lipoprotein and protein ligands. The protein encoded by this gene functions as a receptor or, with Frizzled, a co-receptor for Wnt and thereby transmits the canonical Wnt/beta-catenin signaling cascade. Through its interaction with the Wnt/beta-catenin signaling cascade this gene plays a role in the regulation of cell differentiation, proliferation, and migration and the development of many cancer types. This protein undergoes gamma-secretase dependent RIP- (regulated intramembrane proteolysis) processing but the precise locations of the cleavage sites have not been determined.[provided by RefSeq, Dec 2009]","start":12116025,"end":12267012,"strand":-1,"description":"LDL receptor related protein 6 [Source:HGNC Symbol;Acc:HGNC:6698]"}, {"versioned_ensembl_gene_id":"ENSG00000282467.1","gene_symbol":"AL356131.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":61240898,"end":61241311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281403.1","gene_symbol":"MIR6719","gene_name":"microRNA 6719 [Source:HGNC Symbol;Acc:HGNC:50012]","synonyms":"hsa-mir-6719","biotype":"miRNA","ncbi_id":"102465974","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":39829716,"end":39829802,"strand":-1,"description":"microRNA 6719 [Source:HGNC Symbol;Acc:HGNC:50012]"}, {"versioned_ensembl_gene_id":"ENSG00000282341.1","gene_symbol":"AC245056.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13119808,"end":13120287,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280495.4","gene_symbol":"TRAPPC4","gene_name":"trafficking protein particle complex 4 [Source:HGNC Symbol;Acc:HGNC:19943]","synonyms":"SBDN,PTD009,TRS23","biotype":"protein_coding","ncbi_id":"51399","summary":null,"start":119018432,"end":119025454,"strand":1,"description":"trafficking protein particle complex 4 [Source:HGNC Symbol;Acc:HGNC:19943]"}, {"versioned_ensembl_gene_id":"ENSG00000281987.2","gene_symbol":"PRAMEF26","gene_name":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645359","summary":null,"start":13121732,"end":13128788,"strand":-1,"description":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]"}, {"versioned_ensembl_gene_id":"ENSG00000280548.3","gene_symbol":"FBL","gene_name":"fibrillarin [Source:HGNC Symbol;Acc:HGNC:3599]","synonyms":"FIB,RNU3IP1,Nop1,FLRN","biotype":"protein_coding","ncbi_id":"2091","summary":"This gene product is a component of a nucleolar small nuclear ribonucleoprotein (snRNP) particle thought to participate in the first step in processing preribosomal RNA. It is associated with the U3, U8, and U13 small nuclear RNAs and is located in the dense fibrillar component (DFC) of the nucleolus. The encoded protein contains an N-terminal repetitive domain that is rich in glycine and arginine residues, like fibrillarins in other species. Its central region resembles an RNA-binding domain and contains an RNP consensus sequence. Antisera from approximately 8% of humans with the autoimmune disease scleroderma recognize fibrillarin. [provided by RefSeq, Jul 2008]","start":39834458,"end":39846414,"strand":-1,"description":"fibrillarin [Source:HGNC Symbol;Acc:HGNC:3599]"}, {"versioned_ensembl_gene_id":"ENSG00000281770.1","gene_symbol":"AC018511.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75005112,"end":75027231,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281086.1","gene_symbol":"AC018511.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":75025532,"end":75026308,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284577.1","gene_symbol":"MIR3656","gene_name":"microRNA 3656 [Source:HGNC Symbol;Acc:HGNC:38889]","synonyms":"hsa-mir-3656","biotype":"miRNA","ncbi_id":"100500840","summary":"This record was withdrawn by miRBase.","start":119018944,"end":119019012,"strand":1,"description":"microRNA 3656 [Source:HGNC Symbol;Acc:HGNC:38889]"}, {"versioned_ensembl_gene_id":"ENSG00000281860.1","gene_symbol":"AP003392.12","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119044187,"end":119045492,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281660.1","gene_symbol":"DUPD1","gene_name":"dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23481]","synonyms":"DUSP27","biotype":"protein_coding","ncbi_id":"338599","summary":null,"start":75039893,"end":75060571,"strand":-1,"description":"dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:HGNC:23481]"}, {"versioned_ensembl_gene_id":"ENSG00000283993.1","gene_symbol":"AC245034.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12903108,"end":12903479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283905.1","gene_symbol":"AC245034.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":12907215,"end":12908429,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284215.1","gene_symbol":"AC245056.4","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":12987593,"end":12988702,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280475.1","gene_symbol":"AC007537.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12155262,"end":12155772,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000206783.2","gene_symbol":"RNU6-545P","gene_name":"RNA, U6 small nuclear 545, pseudogene [Source:HGNC Symbol;Acc:HGNC:47508]","synonyms":"RNU6-292P","biotype":"snRNA","ncbi_id":"106479808","summary":null,"start":12226674,"end":12226777,"strand":1,"description":"RNA, U6 small nuclear 545, pseudogene [Source:HGNC Symbol;Acc:HGNC:47508]"}, {"versioned_ensembl_gene_id":"ENSG00000281874.1","gene_symbol":"AC007621.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12248991,"end":12249427,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000207477.2","gene_symbol":"RNU6-318P","gene_name":"RNA, U6 small nuclear 318, pseudogene [Source:HGNC Symbol;Acc:HGNC:47281]","synonyms":"RNU6-1295P","biotype":"snRNA","ncbi_id":"106481589","summary":null,"start":12289227,"end":12289329,"strand":-1,"description":"RNA, U6 small nuclear 318, pseudogene [Source:HGNC Symbol;Acc:HGNC:47281]"}, {"versioned_ensembl_gene_id":"ENSG00000280932.1","gene_symbol":"PRR13P5","gene_name":"proline rich 13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50618]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"440525","summary":null,"start":39958506,"end":39958947,"strand":-1,"description":"proline rich 13 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50618]"}, {"versioned_ensembl_gene_id":"ENSG00000281818.2","gene_symbol":"MANSC1","gene_name":"MANSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25505]","synonyms":"LOH12CR3,FLJ10298","biotype":"protein_coding","ncbi_id":"54682","summary":null,"start":12326056,"end":12350541,"strand":-1,"description":"MANSC domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25505]"}, {"versioned_ensembl_gene_id":"ENSG00000281051.1","gene_symbol":"RPL23AP66","gene_name":"ribosomal protein L23a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35940]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271620","summary":null,"start":12338776,"end":12339254,"strand":1,"description":"ribosomal protein L23a pseudogene 66 [Source:HGNC Symbol;Acc:HGNC:35940]"}, {"versioned_ensembl_gene_id":"ENSG00000281234.1","gene_symbol":"LOH12CR2","gene_name":"loss of heterozygosity, 12, chromosomal region 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26524]","synonyms":"LOH2CR12","biotype":"lincRNA","ncbi_id":"503693","summary":null,"start":12355406,"end":12357067,"strand":-1,"description":"loss of heterozygosity, 12, chromosomal region 2 (non-protein coding) [Source:HGNC Symbol;Acc:HGNC:26524]"}, {"versioned_ensembl_gene_id":"ENSG00000281221.2","gene_symbol":"PSMC4","gene_name":"proteasome 26S subunit, ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9551]","synonyms":"TBP7,TBP-7,S6,MIP224,MGC8570,MGC23214,MGC13687","biotype":"protein_coding","ncbi_id":"5704","summary":"The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the triple-A family of ATPases that is a component of the 19S regulatory subunit and plays a role in 26S proteasome assembly. The encoded protein interacts with gankyrin, a liver oncoprotein, and may also play a role in Parkinson's disease through interactions with synphilin-1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":39986272,"end":39996708,"strand":1,"description":"proteasome 26S subunit, ATPase 4 [Source:HGNC Symbol;Acc:HGNC:9551]"}, {"versioned_ensembl_gene_id":"ENSG00000280689.2","gene_symbol":"BORCS5","gene_name":"BLOC-1 related complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:17950]","synonyms":"LOH1CR12,LOH12CR1","biotype":"protein_coding","ncbi_id":"118426","summary":null,"start":12357079,"end":12469699,"strand":1,"description":"BLOC-1 related complex subunit 5 [Source:HGNC Symbol;Acc:HGNC:17950]"}, {"versioned_ensembl_gene_id":"ENSG00000281168.1","gene_symbol":"AC007619.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12452108,"end":12452486,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280962.2","gene_symbol":"DUSP16","gene_name":"dual specificity phosphatase 16 [Source:HGNC Symbol;Acc:HGNC:17909]","synonyms":"MKP-7,KIAA1700,MKP7","biotype":"protein_coding","ncbi_id":"80824","summary":"This gene encodes a mitogen-activated protein kinase phosphatase that is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. The encoded protein specifically regulates the c-Jun amino-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) pathways.[provided by RefSeq, May 2010]","start":12474215,"end":12562388,"strand":-1,"description":"dual specificity phosphatase 16 [Source:HGNC Symbol;Acc:HGNC:17909]"}, {"versioned_ensembl_gene_id":"ENSG00000282163.1","gene_symbol":"IGKV1-6","gene_name":"immunoglobulin kappa variable 1-6 [Source:HGNC Symbol;Acc:HGNC:5742]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28943","summary":null,"start":88966262,"end":88966767,"strand":-1,"description":"immunoglobulin kappa variable 1-6 [Source:HGNC Symbol;Acc:HGNC:5742]"}, {"versioned_ensembl_gene_id":"ENSG00000280682.2","gene_symbol":"HYOU1","gene_name":"hypoxia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:16931]","synonyms":"ORP150,HSP12A,Grp170","biotype":"protein_coding","ncbi_id":"10525","summary":"The protein encoded by this gene belongs to the heat shock protein 70 family. This gene uses alternative transcription start sites. A cis-acting segment found in the 5' UTR is involved in stress-dependent induction, resulting in the accumulation of this protein in the endoplasmic reticulum (ER) under hypoxic conditions. The protein encoded by this gene is thought to play an important role in protein folding and secretion in the ER. Since suppression of the protein is associated with accelerated apoptosis, it is also suggested to have an important cytoprotective role in hypoxia-induced cellular perturbation. This protein has been shown to be up-regulated in tumors, especially in breast tumors, and thus it is associated with tumor invasiveness. This gene also has an alternative translation initiation site, resulting in a protein that lacks the N-terminal signal peptide. This signal peptide-lacking protein, which is only 3 amino acids shorter than the mature protein in the ER, is thought to have a housekeeping function in the cytosol. In rat, this protein localizes to both the ER by a carboxy-terminal peptide sequence and to mitochondria by an amino-terminal targeting signal. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":119044188,"end":119057201,"strand":-1,"description":"hypoxia up-regulated 1 [Source:HGNC Symbol;Acc:HGNC:16931]"}, {"versioned_ensembl_gene_id":"ENSG00000281671.1","gene_symbol":"AC007619.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":12485358,"end":12491586,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281525.1","gene_symbol":"AC092824.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":12568206,"end":12568781,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284335.1","gene_symbol":"AC007537.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12199641,"end":12200837,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283760.1","gene_symbol":"AC092824.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":12566362,"end":12566733,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281526.2","gene_symbol":"ZNF546","gene_name":"zinc finger protein 546 [Source:HGNC Symbol;Acc:HGNC:28671]","synonyms":"ZNF49,MGC43537","biotype":"protein_coding","ncbi_id":"339327","summary":null,"start":39999401,"end":40036308,"strand":1,"description":"zinc finger protein 546 [Source:HGNC Symbol;Acc:HGNC:28671]"}, {"versioned_ensembl_gene_id":"ENSG00000281233.1","gene_symbol":"AC007842.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":40038651,"end":40040769,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281601.2","gene_symbol":"ZNF780B","gene_name":"zinc finger protein 780B [Source:HGNC Symbol;Acc:HGNC:33109]","synonyms":"ZNF779","biotype":"protein_coding","ncbi_id":"163131","summary":null,"start":40043527,"end":40071476,"strand":-1,"description":"zinc finger protein 780B [Source:HGNC Symbol;Acc:HGNC:33109]"}, {"versioned_ensembl_gene_id":"ENSG00000281009.1","gene_symbol":"AC005614.4","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":40064024,"end":40106192,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280568.2","gene_symbol":"ZNF780A","gene_name":"zinc finger protein 780A [Source:HGNC Symbol;Acc:HGNC:27603]","synonyms":"ZNF780","biotype":"protein_coding","ncbi_id":"284323","summary":null,"start":40084419,"end":40106205,"strand":-1,"description":"zinc finger protein 780A [Source:HGNC Symbol;Acc:HGNC:27603]"}, {"versioned_ensembl_gene_id":"ENSG00000280797.1","gene_symbol":"AC005614.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":40106021,"end":40109673,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281123.2","gene_symbol":"FCGBP","gene_name":"Fc fragment of IgG binding protein [Source:HGNC Symbol;Acc:HGNC:13572]","synonyms":"FC(GAMMA)BP,FC(GAMMA)BP","biotype":"protein_coding","ncbi_id":"8857","summary":null,"start":39863324,"end":39949893,"strand":-1,"description":"Fc fragment of IgG binding protein [Source:HGNC Symbol;Acc:HGNC:13572]"}, {"versioned_ensembl_gene_id":"ENSG00000281163.1","gene_symbol":"AP003392.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":119065262,"end":119065676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280967.1","gene_symbol":"AP003392.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":119067373,"end":119067697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280616.2","gene_symbol":"VPS11","gene_name":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]","synonyms":"PEP5,RNF108","biotype":"protein_coding","ncbi_id":"55823","summary":"Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps11 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":119067691,"end":119081977,"strand":1,"description":"VPS11, CORVET/HOPS core subunit [Source:HGNC Symbol;Acc:HGNC:14583]"}, {"versioned_ensembl_gene_id":"ENSG00000281702.3","gene_symbol":"HMBS","gene_name":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]","synonyms":"UPS,PORC,PBGD","biotype":"protein_coding","ncbi_id":"3145","summary":"This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]","start":119084865,"end":119093548,"strand":1,"description":"hydroxymethylbilane synthase [Source:HGNC Symbol;Acc:HGNC:4982]"}, {"versioned_ensembl_gene_id":"ENSG00000281165.2","gene_symbol":"SLC2A6","gene_name":"solute carrier family 2 member 6 [Source:HGNC Symbol;Acc:HGNC:11011]","synonyms":"GLUT9,GLUT6,HSA011372","biotype":"protein_coding","ncbi_id":"11182","summary":"Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]","start":133471243,"end":133479285,"strand":-1,"description":"solute carrier family 2 member 6 [Source:HGNC Symbol;Acc:HGNC:11011]"}, {"versioned_ensembl_gene_id":"ENSG00000281500.1","gene_symbol":"SLC37A4","gene_name":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]","synonyms":"G6PT1,GSD1d,GSD1c,GSD1b,G6PT3,G6PT2","biotype":"protein_coding","ncbi_id":"2542","summary":"This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009]","start":119024353,"end":119030905,"strand":-1,"description":"solute carrier family 37 member 4 [Source:HGNC Symbol;Acc:HGNC:4061]"}, {"versioned_ensembl_gene_id":"ENSG00000282172.1","gene_symbol":"IGKV5-2","gene_name":"immunoglobulin kappa variable 5-2 [Source:HGNC Symbol;Acc:HGNC:5835]","synonyms":"IGKV52,B2","biotype":"IG_V_gene","ncbi_id":"28907","summary":null,"start":88897232,"end":88897784,"strand":1,"description":"immunoglobulin kappa variable 5-2 [Source:HGNC Symbol;Acc:HGNC:5835]"}, {"versioned_ensembl_gene_id":"ENSG00000283024.1","gene_symbol":"ATAD1","gene_name":"ATPase family, AAA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25903]","synonyms":"FLJ14600","biotype":"protein_coding","ncbi_id":"84896","summary":null,"start":87751512,"end":87841343,"strand":-1,"description":"ATPase family, AAA domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25903]"}, {"versioned_ensembl_gene_id":"ENSG00000282050.1","gene_symbol":"IGKV7-3","gene_name":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28905","summary":null,"start":88915081,"end":88915378,"strand":-1,"description":"immunoglobulin kappa variable 7-3 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5839]"}, {"versioned_ensembl_gene_id":"ENSG00000283114.1","gene_symbol":"NDUFB11P1","gene_name":"NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33980]","synonyms":"NDUFB11P","biotype":"processed_pseudogene","ncbi_id":"390239","summary":null,"start":92340108,"end":92340572,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:33980]"}, {"versioned_ensembl_gene_id":"ENSG00000282699.1","gene_symbol":"PGBD4P5","gene_name":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100421123","summary":null,"start":88922328,"end":88922753,"strand":-1,"description":"piggyBac transposable element derived 4 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:44070]"}, {"versioned_ensembl_gene_id":"ENSG00000282448.1","gene_symbol":"IGKV2-4","gene_name":"immunoglobulin kappa variable 2-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5788]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28929","summary":null,"start":88931666,"end":88932380,"strand":-1,"description":"immunoglobulin kappa variable 2-4 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5788]"}, {"versioned_ensembl_gene_id":"ENSG00000282801.1","gene_symbol":"IGKV1-5","gene_name":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28299","summary":null,"start":88947301,"end":88947957,"strand":-1,"description":"immunoglobulin kappa variable 1-5 [Source:HGNC Symbol;Acc:HGNC:5741]"}, {"versioned_ensembl_gene_id":"ENSG00000282866.1","gene_symbol":"CFL1P1","gene_name":"cofilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28560]","synonyms":"MGC35136,CFLP1","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"142913","summary":null,"start":87817928,"end":87845612,"strand":1,"description":"cofilin 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:28560]"}, {"versioned_ensembl_gene_id":"ENSG00000283756.1","gene_symbol":"LO000005.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":61327250,"end":61339349,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282758.1","gene_symbol":"IGKV1-9","gene_name":"immunoglobulin kappa variable 1-9 [Source:HGNC Symbol;Acc:HGNC:5744]","synonyms":"IGKV19,L8","biotype":"IG_V_gene","ncbi_id":"28941","summary":null,"start":89009982,"end":89010515,"strand":-1,"description":"immunoglobulin kappa variable 1-9 [Source:HGNC Symbol;Acc:HGNC:5744]"}, {"versioned_ensembl_gene_id":"ENSG00000282908.1","gene_symbol":"FAT3","gene_name":"FAT atypical cadherin 3 [Source:HGNC Symbol;Acc:HGNC:23112]","synonyms":"KIAA1989,CDHR10,CDHF15","biotype":"protein_coding","ncbi_id":"120114","summary":null,"start":92356172,"end":92900546,"strand":1,"description":"FAT atypical cadherin 3 [Source:HGNC Symbol;Acc:HGNC:23112]"}, {"versioned_ensembl_gene_id":"ENSG00000282248.1","gene_symbol":"IGKV2-10","gene_name":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28928","summary":null,"start":89019992,"end":89020686,"strand":-1,"description":"immunoglobulin kappa variable 2-10 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5776]"}, {"versioned_ensembl_gene_id":"ENSG00000283092.1","gene_symbol":"RN7SL78P","gene_name":"RNA, 7SL, cytoplasmic 78, pseudogene [Source:HGNC 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{"versioned_ensembl_gene_id":"ENSG00000283067.1","gene_symbol":"MED6P1","gene_name":"mediator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45164]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100128990","summary":null,"start":88048102,"end":88049790,"strand":-1,"description":"mediator complex subunit 6 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45164]"}, {"versioned_ensembl_gene_id":"ENSG00000282603.1","gene_symbol":"IGKV1-13","gene_name":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28939","summary":null,"start":89045995,"end":89046466,"strand":-1,"description":"immunoglobulin kappa variable 1-13 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5731]"}, {"versioned_ensembl_gene_id":"ENSG00000283059.2","gene_symbol":"KLLN","gene_name":"killin, p53-regulated DNA replication inhibitor [Source:HGNC 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The expression of this DNA binding protein is upregulated by transcription factor p53. [provided by RefSeq, Dec 2012]","start":87861956,"end":87862489,"strand":-1,"description":"killin, p53-regulated DNA replication inhibitor [Source:HGNC Symbol;Acc:HGNC:37212]"}, {"versioned_ensembl_gene_id":"ENSG00000282251.1","gene_symbol":"IGKV2-14","gene_name":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28927","summary":null,"start":89078010,"end":89078784,"strand":-1,"description":"immunoglobulin kappa variable 2-14 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5777]"}, {"versioned_ensembl_gene_id":"ENSG00000284073.1","gene_symbol":"AC022016.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":87894049,"end":87942655,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282447.1","gene_symbol":"IGKV3-15","gene_name":"immunoglobulin kappa variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5816]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28913","summary":null,"start":89085177,"end":89085787,"strand":-1,"description":"immunoglobulin kappa variable 3-15 [Source:HGNC Symbol;Acc:HGNC:5816]"}, {"versioned_ensembl_gene_id":"ENSG00000282282.1","gene_symbol":"IGKV1-16","gene_name":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]","synonyms":"L1,IGKV116","biotype":"IG_V_gene","ncbi_id":"28938","summary":null,"start":89099859,"end":89100361,"strand":-1,"description":"immunoglobulin kappa variable 1-16 [Source:HGNC Symbol;Acc:HGNC:5732]"}, {"versioned_ensembl_gene_id":"ENSG00000281978.1","gene_symbol":"IGKV1-17","gene_name":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]","synonyms":"IGKV117,A30","biotype":"IG_V_gene","ncbi_id":"28937","summary":null,"start":89117342,"end":89117844,"strand":-1,"description":"immunoglobulin kappa variable 1-17 [Source:HGNC Symbol;Acc:HGNC:5733]"}, {"versioned_ensembl_gene_id":"ENSG00000282200.1","gene_symbol":"IGKV2-18","gene_name":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28926","summary":null,"start":89128724,"end":89129483,"strand":-1,"description":"immunoglobulin kappa variable 2-18 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5778]"}, {"versioned_ensembl_gene_id":"ENSG00000282244.1","gene_symbol":"IGKV2-19","gene_name":"immunoglobulin kappa variable 2-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5779]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28925","summary":null,"start":89134975,"end":89135257,"strand":-1,"description":"immunoglobulin kappa variable 2-19 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5779]"}, {"versioned_ensembl_gene_id":"ENSG00000282825.1","gene_symbol":"CTIF","gene_name":"cap binding complex dependent translation initiation factor [Source:HGNC Symbol;Acc:HGNC:23925]","synonyms":"KIAA0427","biotype":"protein_coding","ncbi_id":"9811","summary":"CTIF is a component of the CBP80 (NCBP1; MIM 600469)/CBP20 (NCBP2; MIM 605133) translation initiation complex that binds cotranscriptionally to the cap end of nascent mRNA. The CBP80/CBP20 complex is involved in a simultaneous editing and translation step that recognizes premature termination codons (PTCs) in mRNAs and directs PTC-containing mRNAs toward nonsense-mediated decay (NMD). On mRNAs without PTCs, the CBP80/CBP20 complex is replaced with cytoplasmic mRNA cap-binding proteins, including EIF4G (MIM 600495), and steady-state translation of the mRNAs resumes in the cytoplasm (Kim et al., 2009 [PubMed 19648179]).[supplied by OMIM, Dec 2009]","start":48539046,"end":48867468,"strand":1,"description":"cap binding complex dependent translation initiation factor [Source:HGNC Symbol;Acc:HGNC:23925]"}, {"versioned_ensembl_gene_id":"ENSG00000282402.1","gene_symbol":"IGKV3-20","gene_name":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28912","summary":null,"start":89142574,"end":89143160,"strand":-1,"description":"immunoglobulin kappa variable 3-20 [Source:HGNC Symbol;Acc:HGNC:5817]"}, {"versioned_ensembl_gene_id":"ENSG00000282210.1","gene_symbol":"IGKV6-21","gene_name":"immunoglobulin kappa variable 6-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5836]","synonyms":"IGKV621,A26","biotype":"IG_V_gene","ncbi_id":"28906","summary":null,"start":89159751,"end":89160366,"strand":-1,"description":"immunoglobulin kappa variable 6-21 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5836]"}, {"versioned_ensembl_gene_id":"ENSG00000282762.1","gene_symbol":"IGKV1-22","gene_name":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28936","summary":null,"start":89170775,"end":89171212,"strand":-1,"description":"immunoglobulin kappa variable 1-22 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5734]"}, {"versioned_ensembl_gene_id":"ENSG00000282093.1","gene_symbol":"IGKV2-23","gene_name":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28924","summary":null,"start":89172022,"end":89172553,"strand":-1,"description":"immunoglobulin kappa variable 2-23 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5780]"}, {"versioned_ensembl_gene_id":"ENSG00000282671.1","gene_symbol":"IGKV2-24","gene_name":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28923","summary":null,"start":89176328,"end":89177160,"strand":-1,"description":"immunoglobulin kappa variable 2-24 [Source:HGNC Symbol;Acc:HGNC:5781]"}, {"versioned_ensembl_gene_id":"ENSG00000282062.1","gene_symbol":"IGKV3-25","gene_name":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28911","summary":null,"start":89192500,"end":89192752,"strand":-1,"description":"immunoglobulin kappa variable 3-25 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5818]"}, {"versioned_ensembl_gene_id":"ENSG00000282622.1","gene_symbol":"IGKV2-26","gene_name":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28922","summary":null,"start":89196096,"end":89196829,"strand":-1,"description":"immunoglobulin kappa variable 2-26 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5782]"}, {"versioned_ensembl_gene_id":"ENSG00000282000.1","gene_symbol":"AC244255.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":89203509,"end":89203906,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282666.1","gene_symbol":"IGKV1-27","gene_name":"immunoglobulin kappa variable 1-27 [Source:HGNC Symbol;Acc:HGNC:5735]","synonyms":"IGKV127,A20","biotype":"IG_V_gene","ncbi_id":"28935","summary":null,"start":89213423,"end":89213928,"strand":-1,"description":"immunoglobulin kappa variable 1-27 [Source:HGNC Symbol;Acc:HGNC:5735]"}, {"versioned_ensembl_gene_id":"ENSG00000282025.1","gene_symbol":"IGKV2-28","gene_name":"immunoglobulin kappa variable 2-28 [Source:HGNC Symbol;Acc:HGNC:5783]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28921","summary":null,"start":89221698,"end":89222461,"strand":-1,"description":"immunoglobulin kappa variable 2-28 [Source:HGNC Symbol;Acc:HGNC:5783]"}, {"versioned_ensembl_gene_id":"ENSG00000283062.1","gene_symbol":"PGAM1P9","gene_name":"phosphoglycerate mutase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42456]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100420681","summary":null,"start":92370572,"end":92371326,"strand":-1,"description":"phosphoglycerate mutase 1 pseudogene 9 [Source:HGNC Symbol;Acc:HGNC:42456]"}, {"versioned_ensembl_gene_id":"ENSG00000282635.1","gene_symbol":"IGKV2-29","gene_name":"immunoglobulin kappa variable 2-29 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5784]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28920","summary":null,"start":89234174,"end":89234912,"strand":-1,"description":"immunoglobulin kappa variable 2-29 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5784]"}, {"versioned_ensembl_gene_id":"ENSG00000282928.1","gene_symbol":"MAP4K1","gene_name":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]","synonyms":"HPK1","biotype":"protein_coding","ncbi_id":"11184","summary":null,"start":38587641,"end":38618882,"strand":-1,"description":"mitogen-activated protein kinase kinase kinase kinase 1 [Source:HGNC Symbol;Acc:HGNC:6863]"}, {"versioned_ensembl_gene_id":"ENSG00000282929.1","gene_symbol":"AP000722.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":92404267,"end":92412252,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281933.1","gene_symbol":"IGKV2-30","gene_name":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28919","summary":null,"start":89244781,"end":89245596,"strand":-1,"description":"immunoglobulin kappa variable 2-30 [Source:HGNC Symbol;Acc:HGNC:5785]"}, {"versioned_ensembl_gene_id":"ENSG00000282743.1","gene_symbol":"IGKV3-31","gene_name":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28910","summary":null,"start":89252211,"end":89252736,"strand":-1,"description":"immunoglobulin kappa variable 3-31 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5819]"}, {"versioned_ensembl_gene_id":"ENSG00000282571.1","gene_symbol":"IGKV1-32","gene_name":"immunoglobulin kappa variable 1-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5736]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28934","summary":null,"start":89253571,"end":89254015,"strand":-1,"description":"immunoglobulin kappa variable 1-32 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5736]"}, {"versioned_ensembl_gene_id":"ENSG00000282811.1","gene_symbol":"IGKV1-33","gene_name":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]","synonyms":"IGKV133,O18","biotype":"IG_V_gene","ncbi_id":"28933","summary":null,"start":89266494,"end":89268506,"strand":-1,"description":"immunoglobulin kappa variable 1-33 [Source:HGNC Symbol;Acc:HGNC:5737]"}, {"versioned_ensembl_gene_id":"ENSG00000282974.1","gene_symbol":"DPP6","gene_name":"dipeptidyl peptidase like 6 [Source:HGNC Symbol;Acc:HGNC:3010]","synonyms":"DPL1,DPPX","biotype":"protein_coding","ncbi_id":"1804","summary":"This gene encodes a single-pass type II membrane protein that is a member of the peptidase S9B family of serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Variations in this gene may be associated with susceptibility to amyotrophic lateral sclerosis and with idiopathic ventricular fibrillation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]","start":153887097,"end":154893631,"strand":1,"description":"dipeptidyl peptidase like 6 [Source:HGNC Symbol;Acc:HGNC:3010]"}, {"versioned_ensembl_gene_id":"ENSG00000282149.1","gene_symbol":"IGKV3-34","gene_name":"immunoglobulin kappa variable 3-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5820]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28909","summary":null,"start":89275298,"end":89275787,"strand":-1,"description":"immunoglobulin kappa variable 3-34 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5820]"}, {"versioned_ensembl_gene_id":"ENSG00000282157.1","gene_symbol":"IGKV1-35","gene_name":"immunoglobulin kappa variable 1-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5738]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28932","summary":null,"start":89286689,"end":89286973,"strand":-1,"description":"immunoglobulin kappa variable 1-35 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5738]"}, {"versioned_ensembl_gene_id":"ENSG00000282646.1","gene_symbol":"IGKV2-36","gene_name":"immunoglobulin kappa variable 2-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5786]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28918","summary":null,"start":89295233,"end":89295455,"strand":-1,"description":"immunoglobulin kappa variable 2-36 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5786]"}, {"versioned_ensembl_gene_id":"ENSG00000282394.1","gene_symbol":"IGKV1-37","gene_name":"immunoglobulin kappa variable 1-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5739]","synonyms":"O14,IGKV137","biotype":"IG_V_gene","ncbi_id":"28931","summary":null,"start":89297264,"end":89297785,"strand":-1,"description":"immunoglobulin kappa variable 1-37 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5739]"}, {"versioned_ensembl_gene_id":"ENSG00000282387.1","gene_symbol":"IGKV2-38","gene_name":"immunoglobulin kappa variable 2-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5787]","synonyms":null,"biotype":"IG_V_pseudogene","ncbi_id":"28917","summary":null,"start":89309898,"end":89310144,"strand":-1,"description":"immunoglobulin kappa variable 2-38 (pseudogene) [Source:HGNC Symbol;Acc:HGNC:5787]"}, {"versioned_ensembl_gene_id":"ENSG00000282120.1","gene_symbol":"IGKV1-39","gene_name":"immunoglobulin kappa variable 1-39 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5740]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28930","summary":null,"start":89319625,"end":89320146,"strand":-1,"description":"immunoglobulin kappa variable 1-39 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:5740]"}, {"versioned_ensembl_gene_id":"ENSG00000282182.1","gene_symbol":"IGKV2-40","gene_name":"immunoglobulin kappa variable 2-40 [Source:HGNC Symbol;Acc:HGNC:5789]","synonyms":null,"biotype":"IG_V_gene","ncbi_id":"28916","summary":null,"start":89330110,"end":89330429,"strand":-1,"description":"immunoglobulin kappa variable 2-40 [Source:HGNC Symbol;Acc:HGNC:5789]"}, {"versioned_ensembl_gene_id":"ENSG00000283080.1","gene_symbol":"AC048380.4","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48564795,"end":48568342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282900.2","gene_symbol":"MIR4743","gene_name":"microRNA 4743 [Source:HGNC Symbol;Acc:HGNC:41894]","synonyms":"hsa-mir-4743","biotype":"miRNA","ncbi_id":"100616366","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":48670632,"end":48670700,"strand":1,"description":"microRNA 4743 [Source:HGNC Symbol;Acc:HGNC:41894]"}, {"versioned_ensembl_gene_id":"ENSG00000282959.1","gene_symbol":"AC022919.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48677826,"end":48692670,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283002.1","gene_symbol":"AC022919.3","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":48759944,"end":48760569,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283068.1","gene_symbol":"IBTK","gene_name":"inhibitor of Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:17853]","synonyms":"DKFZP564B116,BTKI,BTBD26","biotype":"protein_coding","ncbi_id":"25998","summary":"Bruton tyrosine kinase (BTK) is a protein tyrosine kinase that is expressed in B cells, macrophages, and neutrophils. The protein encoded by this gene binds to BTK and downregulates BTK's kinase activity. In addition, the encoded protein disrupts BTK-mediated calcium mobilization and negatively regulates the activation of nuclear factor-kappa-B-driven transcription. This gene has a pseudogene on chromosome 18. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]","start":82169983,"end":82247754,"strand":-1,"description":"inhibitor of Bruton tyrosine kinase [Source:HGNC Symbol;Acc:HGNC:17853]"}, {"versioned_ensembl_gene_id":"ENSG00000282923.1","gene_symbol":"AC093567.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":48830302,"end":48839021,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283593.1","gene_symbol":"TUBB7P","gene_name":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]","synonyms":"TUBB4Q","biotype":"unprocessed_pseudogene","ncbi_id":"56604","summary":null,"start":189982523,"end":189984871,"strand":-1,"description":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]"}, {"versioned_ensembl_gene_id":"ENSG00000283939.1","gene_symbol":"U4","gene_name":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]","synonyms":null,"biotype":"snRNA","ncbi_id":null,"summary":null,"start":179492015,"end":179492096,"strand":-1,"description":"U4 spliceosomal RNA [Source:RFAM;Acc:RF00015]"}, {"versioned_ensembl_gene_id":"ENSG00000283896.1","gene_symbol":"AC270306.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179503254,"end":179515530,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282956.1","gene_symbol":"MAGI1","gene_name":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]","synonyms":"AIP3,WWP3,TNRC19,MAGI-1,BAP1,BAIAP1","biotype":"protein_coding","ncbi_id":"9223","summary":"The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","start":65353525,"end":66038834,"strand":-1,"description":"membrane associated guanylate kinase, WW and PDZ domain containing 1 [Source:HGNC Symbol;Acc:HGNC:946]"}, {"versioned_ensembl_gene_id":"ENSG00000282095.1","gene_symbol":"HNRNPCL4","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060301","summary":null,"start":13137413,"end":13138294,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]"}, {"versioned_ensembl_gene_id":"ENSG00000282298.1","gene_symbol":"PRAMEF9","gene_name":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343070","summary":null,"start":13145282,"end":13152291,"strand":1,"description":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]"}, {"versioned_ensembl_gene_id":"ENSG00000282741.2","gene_symbol":"PRAMEF13","gene_name":"PRAME family member 13 [Source:HGNC Symbol;Acc:HGNC:13262]","synonyms":"OTTHUMG00000008034","biotype":"protein_coding","ncbi_id":"400736","summary":null,"start":13169157,"end":13174236,"strand":-1,"description":"PRAME family member 13 [Source:HGNC Symbol;Acc:HGNC:13262]"}, {"versioned_ensembl_gene_id":"ENSG00000282212.2","gene_symbol":"PRAMEF18","gene_name":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391003","summary":null,"start":13195532,"end":13198933,"strand":-1,"description":"PRAME family member 18 [Source:HGNC Symbol;Acc:HGNC:30693]"}, {"versioned_ensembl_gene_id":"ENSG00000282289.1","gene_symbol":"PRAMEF31P","gene_name":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129611","summary":null,"start":13218690,"end":13221479,"strand":1,"description":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]"}, {"versioned_ensembl_gene_id":"ENSG00000282424.1","gene_symbol":"PRAMEF5","gene_name":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]","synonyms":"PRAMEF5L,PRAMEF23","biotype":"protein_coding","ncbi_id":"343068","summary":null,"start":13227039,"end":13236141,"strand":1,"description":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]"}, {"versioned_ensembl_gene_id":"ENSG00000282216.1","gene_symbol":"PRAMEF32P","gene_name":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"650236","summary":null,"start":13246366,"end":13248454,"strand":-1,"description":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]"}, {"versioned_ensembl_gene_id":"ENSG00000282288.1","gene_symbol":"RNU6-443P","gene_name":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481318","summary":null,"start":13251952,"end":13252058,"strand":-1,"description":"RNA, U6 small nuclear 443, pseudogene [Source:HGNC Symbol;Acc:HGNC:47406]"}, {"versioned_ensembl_gene_id":"ENSG00000282583.1","gene_symbol":"PRAMEF8","gene_name":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391002","summary":null,"start":13253862,"end":13258001,"strand":-1,"description":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]"}, {"versioned_ensembl_gene_id":"ENSG00000282125.2","gene_symbol":"PRAMEF33","gene_name":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]","synonyms":"PRAMEF33P,PRAMEF33P","biotype":"protein_coding","ncbi_id":"645382","summary":null,"start":13276366,"end":13281734,"strand":1,"description":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]"}, {"versioned_ensembl_gene_id":"ENSG00000282982.1","gene_symbol":"AC008649.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38596346,"end":38601694,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283976.1","gene_symbol":"AC244216.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":13185912,"end":13187021,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284080.1","gene_symbol":"AC244216.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":13271139,"end":13271510,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282986.1","gene_symbol":"EIF3K","gene_name":"eukaryotic translation initiation factor 3 subunit K [Source:HGNC Symbol;Acc:HGNC:24656]","synonyms":"PTD001,PRO1474,PLAC-24,M9,HSPC029,EIF3S12,eIF3k,ARG134","biotype":"protein_coding","ncbi_id":"27335","summary":"The 700-kD eukaryotic translation initiation factor-3 (eIF3) is the largest eIF and contains at least 12 subunits, including EIF2S12. eIF3 plays an essential role in translation by binding directly to the 40S ribosomal subunit and promoting formation of the 40S preinitiation complex (Mayeur et al., 2003 [PubMed 14519125]).[supplied by OMIM, Mar 2008]","start":38619082,"end":38636955,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit K [Source:HGNC Symbol;Acc:HGNC:24656]"}, {"versioned_ensembl_gene_id":"ENSG00000282867.1","gene_symbol":"RNU6-130P","gene_name":"RNA, U6 small nuclear 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:47093]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481218","summary":null,"start":82210338,"end":82210440,"strand":-1,"description":"RNA, U6 small nuclear 130, pseudogene [Source:HGNC Symbol;Acc:HGNC:47093]"}, {"versioned_ensembl_gene_id":"ENSG00000282877.1","gene_symbol":"AC209420.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":82274199,"end":82275177,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283085.1","gene_symbol":"TPBG","gene_name":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]","synonyms":"5T4-AG,5T4","biotype":"protein_coding","ncbi_id":"7162","summary":"This gene encodes a leucine-rich transmembrane glycoprotein that may be involved in cell adhesion. The encoded protein is an oncofetal antigen that is specific to trophoblast cells. In adults this protein is highly expressed in many tumor cells and is associated with poor clinical outcome in numerous cancers. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]","start":82373409,"end":82381031,"strand":1,"description":"trophoblast glycoprotein [Source:HGNC Symbol;Acc:HGNC:12004]"}, {"versioned_ensembl_gene_id":"ENSG00000282844.1","gene_symbol":"ACTN4","gene_name":"actinin alpha 4 [Source:HGNC Symbol;Acc:HGNC:166]","synonyms":"FSGS1","biotype":"protein_coding","ncbi_id":"81","summary":" Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a nonmuscle, alpha actinin isoform which is concentrated in the cytoplasm, and thought to be involved in metastatic processes. Mutations in this gene have been associated with focal and segmental glomerulosclerosis. [provided by RefSeq, Jul 2008]","start":38647649,"end":38731583,"strand":1,"description":"actinin alpha 4 [Source:HGNC Symbol;Acc:HGNC:166]"}, {"versioned_ensembl_gene_id":"ENSG00000282739.1","gene_symbol":"SLC25A26","gene_name":"solute carrier family 25 member 26 [Source:HGNC Symbol;Acc:HGNC:20661]","synonyms":null,"biotype":"protein_coding","ncbi_id":"115286","summary":"This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]","start":66133610,"end":66388212,"strand":1,"description":"solute carrier family 25 member 26 [Source:HGNC Symbol;Acc:HGNC:20661]"}, {"versioned_ensembl_gene_id":"ENSG00000282976.1","gene_symbol":"AC008649.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38683873,"end":38693606,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282869.1","gene_symbol":"AC256309.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38738251,"end":38739830,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282902.1","gene_symbol":"LGALS7B","gene_name":"galectin 7B [Source:HGNC Symbol;Acc:HGNC:34447]","synonyms":"GAL7","biotype":"protein_coding","ncbi_id":"653499","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:3963) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008]","start":38770974,"end":38773512,"strand":-1,"description":"galectin 7B [Source:HGNC Symbol;Acc:HGNC:34447]"}, {"versioned_ensembl_gene_id":"ENSG00000283700.1","gene_symbol":"RNA5SP174","gene_name":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]","synonyms":"RN5S174","biotype":"rRNA","ncbi_id":"106478998","summary":null,"start":190014800,"end":190014917,"strand":1,"description":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]"}, {"versioned_ensembl_gene_id":"ENSG00000283082.1","gene_symbol":"LGALS7","gene_name":"galectin 7 [Source:HGNC Symbol;Acc:HGNC:6568]","synonyms":"LGALS7A,GAL7,TP53I1,PIG1","biotype":"protein_coding","ncbi_id":"3963","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:653499) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008]","start":38789280,"end":38791794,"strand":1,"description":"galectin 7 [Source:HGNC Symbol;Acc:HGNC:6568]"}, {"versioned_ensembl_gene_id":"ENSG00000283011.1","gene_symbol":"RNU6-140P","gene_name":"RNA, U6 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:47103]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481221","summary":null,"start":38797048,"end":38797155,"strand":-1,"description":"RNA, U6 small nuclear 140, pseudogene [Source:HGNC Symbol;Acc:HGNC:47103]"}, {"versioned_ensembl_gene_id":"ENSG00000282510.1","gene_symbol":"RNU6-787P","gene_name":"RNA, U6 small nuclear 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:47750]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479914","summary":null,"start":66293210,"end":66293316,"strand":-1,"description":"RNA, U6 small nuclear 787, pseudogene [Source:HGNC Symbol;Acc:HGNC:47750]"}, {"versioned_ensembl_gene_id":"ENSG00000282585.1","gene_symbol":"RN7SL482P","gene_name":"RNA, 7SL, cytoplasmic 482, pseudogene [Source:HGNC Symbol;Acc:HGNC:46498]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480513","summary":null,"start":66323951,"end":66324248,"strand":1,"description":"RNA, 7SL, cytoplasmic 482, pseudogene [Source:HGNC Symbol;Acc:HGNC:46498]"}, {"versioned_ensembl_gene_id":"ENSG00000282992.1","gene_symbol":"LGALS4","gene_name":"galectin 4 [Source:HGNC Symbol;Acc:HGNC:6565]","synonyms":"GAL4","biotype":"protein_coding","ncbi_id":"3960","summary":"The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. The expression of this gene is restricted to small intestine, colon, and rectum, and it is underexpressed in colorectal cancer. [provided by RefSeq, Jul 2008]","start":38801718,"end":38813400,"strand":-1,"description":"galectin 4 [Source:HGNC Symbol;Acc:HGNC:6565]"}, {"versioned_ensembl_gene_id":"ENSG00000282243.1","gene_symbol":"LRIG1","gene_name":"leucine rich repeats and immunoglobulin like domains 1 [Source:HGNC Symbol;Acc:HGNC:17360]","synonyms":"LIG-1,DKFZP586O1624,LIG1","biotype":"protein_coding","ncbi_id":"26018","summary":null,"start":66378893,"end":66501359,"strand":-1,"description":"leucine rich repeats and immunoglobulin like domains 1 [Source:HGNC Symbol;Acc:HGNC:17360]"}, {"versioned_ensembl_gene_id":"ENSG00000282853.1","gene_symbol":"ECH1","gene_name":"enoyl-CoA hydratase 1 [Source:HGNC Symbol;Acc:HGNC:3149]","synonyms":"HPXEL","biotype":"protein_coding","ncbi_id":"1891","summary":"This gene encodes a member of the hydratase/isomerase superfamily. The gene product shows high sequence similarity to enoyl-coenzyme A (CoA) hydratases of several species, particularly within a conserved domain characteristic of these proteins. The encoded protein, which contains a C-terminal peroxisomal targeting sequence, localizes to the peroxisome. The rat ortholog, which localizes to the matrix of both the peroxisome and mitochondria, can isomerize 3-trans,5-cis-dienoyl-CoA to 2-trans,4-trans-dienoyl-CoA, indicating that it is a delta3,5-delta2,4-dienoyl-CoA isomerase. This enzyme functions in the auxiliary step of the fatty acid beta-oxidation pathway. Expression of the rat gene is induced by peroxisome proliferators. [provided by RefSeq, Jul 2008]","start":38815458,"end":38832041,"strand":-1,"description":"enoyl-CoA hydratase 1 [Source:HGNC Symbol;Acc:HGNC:3149]"}, {"versioned_ensembl_gene_id":"ENSG00000282832.1","gene_symbol":"AC008982.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38817507,"end":38840214,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283077.1","gene_symbol":"AC104534.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38820202,"end":38823259,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282947.1","gene_symbol":"HNRNPL","gene_name":"heterogeneous nuclear ribonucleoprotein L [Source:HGNC Symbol;Acc:HGNC:5045]","synonyms":"HNRPL","biotype":"protein_coding","ncbi_id":"3191","summary":"Heterogeneous nuclear RNAs (hnRNAs) which include mRNA precursors and mature mRNAs are associated with specific proteins to form heterogenous ribonucleoprotein (hnRNP) complexes. Heterogeneous nuclear ribonucleoprotein L is among the proteins that are stably associated with hnRNP complexes and along with other hnRNP proteins is likely to play a major role in the formation, packaging, processing, and function of mRNA. Heterogeneous nuclear ribonucleoprotein L is present in the nucleoplasm as part of the HNRP complex. HNRP proteins have also been identified outside of the nucleoplasm. Exchange of hnRNP for mRNA-binding proteins accompanies transport of mRNA from the nucleus to the cytoplasm. Since HNRP proteins have been shown to shuttle between the nucleus and the cytoplasm, it is possible that they also have cytoplasmic functions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","start":38836424,"end":38852383,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein L [Source:HGNC Symbol;Acc:HGNC:5045]"}, {"versioned_ensembl_gene_id":"ENSG00000283807.1","gene_symbol":"AC256309.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38797363,"end":38797740,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283890.1","gene_symbol":"AC104534.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38807623,"end":38807811,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284345.1","gene_symbol":"AC091493.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":16687986,"end":16697479,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284109.1","gene_symbol":"CDYLP1","gene_name":"chromodomain Y-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52805]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100132260","summary":null,"start":16692745,"end":16694202,"strand":-1,"description":"chromodomain Y-like pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:52805]"}, {"versioned_ensembl_gene_id":"ENSG00000284017.1","gene_symbol":"PLCL2","gene_name":"phospholipase C like 2 [Source:HGNC Symbol;Acc:HGNC:9064]","synonyms":"PLCE2,KIAA1092","biotype":"protein_coding","ncbi_id":"23228","summary":null,"start":16802651,"end":17090572,"strand":1,"description":"phospholipase C like 2 [Source:HGNC Symbol;Acc:HGNC:9064]"}, {"versioned_ensembl_gene_id":"ENSG00000283595.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":50669804,"end":50669901,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283530.1","gene_symbol":"MGAT4C","gene_name":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]","synonyms":"HGNT-IV-H","biotype":"protein_coding","ncbi_id":"25834","summary":null,"start":85955666,"end":86838884,"strand":-1,"description":"MGAT4 family member C [Source:HGNC Symbol;Acc:HGNC:30871]"}, {"versioned_ensembl_gene_id":"ENSG00000283264.1","gene_symbol":"RNU6-409P","gene_name":"RNA, U6 small nuclear 409, pseudogene [Source:HGNC Symbol;Acc:HGNC:47372]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481307","summary":null,"start":50691077,"end":50691180,"strand":-1,"description":"RNA, U6 small nuclear 409, pseudogene [Source:HGNC Symbol;Acc:HGNC:47372]"}, {"versioned_ensembl_gene_id":"ENSG00000284058.1","gene_symbol":"RNA5SP266","gene_name":"RNA, 5S ribosomal pseudogene 266 [Source:HGNC Symbol;Acc:HGNC:43166]","synonyms":"RN5S266","biotype":"rRNA","ncbi_id":"100873519","summary":null,"start":57132453,"end":57132560,"strand":-1,"description":"RNA, 5S ribosomal pseudogene 266 [Source:HGNC Symbol;Acc:HGNC:43166]"}, {"versioned_ensembl_gene_id":"ENSG00000283539.1","gene_symbol":"ACR","gene_name":"acrosin [Source:HGNC Symbol;Acc:HGNC:126]","synonyms":null,"biotype":"protein_coding","ncbi_id":"49","summary":"Acrosin is the major proteinase present in the acrosome of mature spermatozoa. It is a typical serine proteinase with trypsin-like specificity. It is stored in the acrosome in its precursor form, proacrosin. The active enzyme functions in the lysis of the zona pellucida, thus facilitating penetration of the sperm through the innermost glycoprotein layers of the ovum. The mRNA for proacrosin is synthesized only in the postmeiotic stages of spermatogenesis. In humans proacrosin first appears in the haploid spermatids. [provided by RefSeq, Jul 2008]","start":50738219,"end":50745351,"strand":1,"description":"acrosin [Source:HGNC Symbol;Acc:HGNC:126]"}, {"versioned_ensembl_gene_id":"ENSG00000283243.1","gene_symbol":"SHANK3","gene_name":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]","synonyms":"SPANK-2,PSAP2,prosap2,KIAA1650","biotype":"protein_coding","ncbi_id":"85358","summary":"This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]","start":50674637,"end":50733232,"strand":1,"description":"SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:HGNC:14294]"}, {"versioned_ensembl_gene_id":"ENSG00000284096.1","gene_symbol":"PRKAR2B","gene_name":"protein kinase cAMP-dependent type II regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9392]","synonyms":"PRKAR2","biotype":"protein_coding","ncbi_id":"5577","summary":"cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. The protein encoded by this gene is one of the regulatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. This subunit has been shown to interact with and suppress the transcriptional activity of the cAMP responsive element binding protein 1 (CREB1) in activated T cells. Knockout studies in mice suggest that this subunit may play an important role in regulating energy balance and adiposity. The studies also suggest that this subunit may mediate the gene induction and cataleptic behavior induced by haloperidol. [provided by RefSeq, Jul 2008]","start":107044649,"end":107161811,"strand":1,"description":"protein kinase cAMP-dependent type II regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:9392]"}, {"versioned_ensembl_gene_id":"ENSG00000283668.1","gene_symbol":"AF250324.9","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189780336,"end":189940271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283802.1","gene_symbol":"ADAMTS2","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 2 [Source:HGNC Symbol;Acc:HGNC:218]","synonyms":"hPCPNI,ADAMTS-3,ADAM-TS2,PCINP,NPI","biotype":"protein_coding","ncbi_id":"9509","summary":"This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]","start":179110851,"end":179345430,"strand":-1,"description":"ADAM metallopeptidase with thrombospondin type 1 motif 2 [Source:HGNC Symbol;Acc:HGNC:218]"}, {"versioned_ensembl_gene_id":"ENSG00000283350.1","gene_symbol":"MUC6","gene_name":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]","synonyms":null,"biotype":"protein_coding","ncbi_id":"4588","summary":"This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. [provided by RefSeq, Dec 2016]","start":1012821,"end":1036706,"strand":-1,"description":"mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]"}, {"versioned_ensembl_gene_id":"ENSG00000283960.1","gene_symbol":"MIR3714","gene_name":"microRNA 3714 [Source:HGNC Symbol;Acc:HGNC:38928]","synonyms":"hsa-mir-3714","biotype":"miRNA","ncbi_id":"100500913","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":16933174,"end":16933238,"strand":1,"description":"microRNA 3714 [Source:HGNC Symbol;Acc:HGNC:38928]"}, {"versioned_ensembl_gene_id":"ENSG00000284477.1","gene_symbol":"PLCL2-AS1","gene_name":"PLCL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40449]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100874003","summary":null,"start":17042720,"end":17044170,"strand":-1,"description":"PLCL2 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40449]"}, {"versioned_ensembl_gene_id":"ENSG00000284398.1","gene_symbol":"AC210544.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":57070985,"end":57071356,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284599.1","gene_symbol":"AC091491.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":16979511,"end":16979882,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283287.1","gene_symbol":"FO681507.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":50740616,"end":50743537,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283252.1","gene_symbol":"AC002056.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":50754693,"end":50755452,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284126.1","gene_symbol":"SMURF1","gene_name":"SMAD specific E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:16807]","synonyms":"KIAA1625","biotype":"protein_coding","ncbi_id":"57154","summary":"This gene encodes a ubiquitin ligase that is specific for receptor-regulated SMAD proteins in the bone morphogenetic protein (BMP) pathway. This protein plays a key roll in the regulation of cell motility, cell signalling, and cell polarity. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2010]","start":99027438,"end":99144100,"strand":-1,"description":"SMAD specific E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:HGNC:16807]"}, {"versioned_ensembl_gene_id":"ENSG00000283153.1","gene_symbol":"FRG1","gene_name":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]","synonyms":"FSG1,FRG1A","biotype":"protein_coding","ncbi_id":"2483","summary":"This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]","start":189940788,"end":189963204,"strand":1,"description":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]"}, {"versioned_ensembl_gene_id":"ENSG00000283658.1","gene_symbol":"RPL23AP82","gene_name":"ribosomal protein L23a pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:33730]","synonyms":"MGC70863","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"284942","summary":null,"start":50756966,"end":50801327,"strand":1,"description":"ribosomal protein L23a pseudogene 82 [Source:HGNC Symbol;Acc:HGNC:33730]"}, {"versioned_ensembl_gene_id":"ENSG00000283640.1","gene_symbol":"AC256300.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":1049876,"end":1055745,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283651.1","gene_symbol":"AC010196.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":86599578,"end":86838978,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283163.1","gene_symbol":"AC079597.2","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":87041747,"end":87042254,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284273.1","gene_symbol":"AC079597.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":86938860,"end":86939523,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283158.1","gene_symbol":"MUC5AC","gene_name":"mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7515]","synonyms":"MUC5","biotype":"protein_coding","ncbi_id":"4586","summary":null,"start":1159911,"end":1203106,"strand":1,"description":"mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7515]"}, {"versioned_ensembl_gene_id":"ENSG00000284315.1","gene_symbol":"AC109479.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179377505,"end":179378865,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283847.1","gene_symbol":"HBP1","gene_name":"HMG-box transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:23200]","synonyms":null,"biotype":"protein_coding","ncbi_id":"26959","summary":null,"start":107168961,"end":107202529,"strand":1,"description":"HMG-box transcription factor 1 [Source:HGNC Symbol;Acc:HGNC:23200]"}, {"versioned_ensembl_gene_id":"ENSG00000284358.1","gene_symbol":"AC109479.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179377531,"end":179378761,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283508.1","gene_symbol":"MLLT10P2","gene_name":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480724","summary":null,"start":189973599,"end":189973847,"strand":-1,"description":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]"}, {"versioned_ensembl_gene_id":"ENSG00000284579.1","gene_symbol":"AC109479.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179385819,"end":179385992,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283581.1","gene_symbol":"RNA5SP175","gene_name":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]","synonyms":"RN5S175","biotype":"rRNA","ncbi_id":"106480758","summary":null,"start":190017360,"end":190017478,"strand":1,"description":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]"}, {"versioned_ensembl_gene_id":"ENSG00000284549.1","gene_symbol":"AC270306.6","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":179522252,"end":179524868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283181.1","gene_symbol":"DUX4L9","gene_name":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288711","summary":null,"start":190021078,"end":190022336,"strand":-1,"description":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]"}, {"versioned_ensembl_gene_id":"ENSG00000283449.1","gene_symbol":"RARRES2P4","gene_name":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644881","summary":null,"start":190037743,"end":190038226,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]"}, {"versioned_ensembl_gene_id":"ENSG00000283363.1","gene_symbol":"DUX4L8","gene_name":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]","synonyms":"DUX2","biotype":"unprocessed_pseudogene","ncbi_id":"26583","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190067620,"end":190068894,"strand":1,"description":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]"}, {"versioned_ensembl_gene_id":"ENSG00000284124.1","gene_symbol":"AC270306.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":179527020,"end":179527309,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283660.1","gene_symbol":"RPL23AP84","gene_name":"ribosomal protein L23a pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:51575]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"102723981","summary":null,"start":190128676,"end":190129139,"strand":1,"description":"ribosomal protein L23a pseudogene 84 [Source:HGNC Symbol;Acc:HGNC:51575]"}, {"versioned_ensembl_gene_id":"ENSG00000283223.1","gene_symbol":"AC215524.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":190128687,"end":190128927,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284383.1","gene_symbol":"CT476828.18","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190070926,"end":190072197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284496.1","gene_symbol":"CT476828.20","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190074232,"end":190075503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284262.1","gene_symbol":"CT476828.17","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190077538,"end":190078809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283767.1","gene_symbol":"CT476828.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190080844,"end":190082115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284210.1","gene_symbol":"CT476828.16","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190084150,"end":190085421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283884.1","gene_symbol":"CT476828.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190087456,"end":190088727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283955.1","gene_symbol":"CT476828.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190090762,"end":190092033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284025.1","gene_symbol":"CT476828.11","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190094068,"end":190095339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283878.1","gene_symbol":"CT476828.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190097374,"end":190098645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284181.1","gene_symbol":"CT476828.15","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190100680,"end":190101951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283820.1","gene_symbol":"CT476828.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190103986,"end":190105257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283949.1","gene_symbol":"DUX4","gene_name":"double homeobox 4 [Source:HGNC Symbol;Acc:HGNC:50800]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288687","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length; a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. The encoded protein has been reported to function as a transcriptional activator of paired-like homeodomain transcription factor 1 (PITX1; GeneID 5307). Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]","start":190107292,"end":190108563,"strand":1,"description":"double homeobox 4 [Source:HGNC Symbol;Acc:HGNC:50800]"}, {"versioned_ensembl_gene_id":"ENSG00000284050.1","gene_symbol":"AC256300.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":1094215,"end":1105829,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284068.1","gene_symbol":"KPNA7","gene_name":"karyopherin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:21839]","synonyms":"IPOA8","biotype":"protein_coding","ncbi_id":"402569","summary":"The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC), which consists of 60-100 proteins. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion while larger molecules are transported by an active process. The protein encoded by this gene belongs to the importin alpha family, and is involved in nuclear protein import, but exhibits different nuclear localization signal binding specificity compared to other members of the family. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, Jul 2016]","start":99173574,"end":99207506,"strand":-1,"description":"karyopherin subunit alpha 7 [Source:HGNC Symbol;Acc:HGNC:21839]"}, {"versioned_ensembl_gene_id":"ENSG00000284260.1","gene_symbol":"RUFY1","gene_name":"RUN and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19760]","synonyms":"ZFYVE12,RABIP4,FLJ22251","biotype":"protein_coding","ncbi_id":"80230","summary":"This gene encodes a protein that contains a RUN domain and a FYVE-type zinc finger domain. The encoded protein binds to phosphatidylinositol-3-phosphate (PI3P) and plays a role in early endosomal trafficking, tethering and fusion through interactions with small GTPases including Rab4, Rab5 and Rab14. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","start":179550493,"end":179611580,"strand":1,"description":"RUN and FYVE domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19760]"}, {"versioned_ensembl_gene_id":"ENSG00000284406.1","gene_symbol":"AC004492.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107192559,"end":107193300,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284369.1","gene_symbol":"COG5","gene_name":"component of oligomeric golgi complex 5 [Source:HGNC Symbol;Acc:HGNC:14857]","synonyms":"GTC90,GOLTC1","biotype":"protein_coding","ncbi_id":"10466","summary":"The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011]","start":107201555,"end":107564647,"strand":-1,"description":"component of oligomeric golgi complex 5 [Source:HGNC Symbol;Acc:HGNC:14857]"}, {"versioned_ensembl_gene_id":"ENSG00000284556.1","gene_symbol":"PRDX2P3","gene_name":"peroxiredoxin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44968]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100418943","summary":null,"start":179572092,"end":179572677,"strand":1,"description":"peroxiredoxin 2 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:44968]"}, {"versioned_ensembl_gene_id":"ENSG00000283808.1","gene_symbol":"AC270306.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":179597471,"end":179605295,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284069.1","gene_symbol":"Metazoa_SRP","gene_name":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":179630732,"end":179630991,"strand":1,"description":"Metazoan signal recognition particle RNA [Source:RFAM;Acc:RF00017]"}, {"versioned_ensembl_gene_id":"ENSG00000284506.1","gene_symbol":"AC270227.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":179641610,"end":179642783,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283718.1","gene_symbol":"CBY3","gene_name":"chibby family member 3 [Source:HGNC Symbol;Acc:HGNC:33278]","synonyms":null,"biotype":"protein_coding","ncbi_id":"646019","summary":null,"start":179679567,"end":179681959,"strand":-1,"description":"chibby family member 3 [Source:HGNC Symbol;Acc:HGNC:33278]"}, {"versioned_ensembl_gene_id":"ENSG00000284045.1","gene_symbol":"AC255406.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":107450200,"end":107450479,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283812.1","gene_symbol":"GPR22","gene_name":"G protein-coupled receptor 22 [Source:HGNC Symbol;Acc:HGNC:4477]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2845","summary":"This gene is a member of the G-protein coupled receptor 1 family and encodes a multi-pass membrane protein. [provided by RefSeq, Jul 2008]","start":107470143,"end":107475785,"strand":1,"description":"G protein-coupled receptor 22 [Source:HGNC Symbol;Acc:HGNC:4477]"}, {"versioned_ensembl_gene_id":"ENSG00000284226.1","gene_symbol":"AC243614.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21537276,"end":21537583,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284103.1","gene_symbol":"DUS4L","gene_name":"dihydrouridine synthase 4 like [Source:HGNC Symbol;Acc:HGNC:21517]","synonyms":"PP35,DUS4","biotype":"protein_coding","ncbi_id":"11062","summary":null,"start":107563617,"end":107578597,"strand":1,"description":"dihydrouridine synthase 4 like [Source:HGNC Symbol;Acc:HGNC:21517]"}, {"versioned_ensembl_gene_id":"ENSG00000283777.1","gene_symbol":"CANX","gene_name":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]","synonyms":"P90,IP90,CNX","biotype":"protein_coding","ncbi_id":"821","summary":"This gene encodes a member of the calnexin family of molecular chaperones. The encoded protein is a calcium-binding, endoplasmic reticulum (ER)-associated protein that interacts transiently with newly synthesized N-linked glycoproteins, facilitating protein folding and assembly. It may also play a central role in the quality control of protein folding by retaining incorrectly folded protein subunits within the ER for degradation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2018]","start":179679612,"end":179731798,"strand":1,"description":"calnexin [Source:HGNC Symbol;Acc:HGNC:1473]"}, {"versioned_ensembl_gene_id":"ENSG00000284582.1","gene_symbol":"AC004839.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":107579690,"end":107580190,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283852.1","gene_symbol":"BCAP29","gene_name":"B-cell receptor associated protein 29 [Source:HGNC Symbol;Acc:HGNC:24131]","synonyms":"DKFZp686M2086,BAP29","biotype":"protein_coding","ncbi_id":"55973","summary":null,"start":107580110,"end":107629303,"strand":1,"description":"B-cell receptor associated protein 29 [Source:HGNC Symbol;Acc:HGNC:24131]"}, {"versioned_ensembl_gene_id":"ENSG00000284201.1","gene_symbol":"snoU109","gene_name":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":107603496,"end":107603640,"strand":1,"description":"Small nucleolar RNA U109 [Source:RFAM;Acc:RF01233]"}, {"versioned_ensembl_gene_id":"ENSG00000284207.1","gene_symbol":"HMGB3P22","gene_name":"high mobility group box 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39314]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"729595","summary":null,"start":179680016,"end":179695621,"strand":1,"description":"high mobility group box 3 pseudogene 22 [Source:HGNC Symbol;Acc:HGNC:39314]"}, {"versioned_ensembl_gene_id":"ENSG00000283780.2","gene_symbol":"MAML1","gene_name":"mastermind like transcriptional coactivator 1 [Source:HGNC Symbol;Acc:HGNC:13632]","synonyms":"Mam-1,KIAA0200","biotype":"protein_coding","ncbi_id":"9794","summary":"This protein is the human homolog of mastermind, a Drosophila protein that plays a role in the Notch signaling pathway involved in cell-fate determination. There is in vitro evidence that the human homolog forms a complex with the intracellular portion of human Notch receptors and can increase expression of a Notch-induced gene. This evidence supports its proposed function as a transcriptional co-activator in the Notch signaling pathway. [provided by RefSeq, Jul 2008]","start":179733723,"end":179778173,"strand":1,"description":"mastermind like transcriptional coactivator 1 [Source:HGNC Symbol;Acc:HGNC:13632]"}, {"versioned_ensembl_gene_id":"ENSG00000283887.1","gene_symbol":"LTC4S","gene_name":"leukotriene C4 synthase [Source:HGNC Symbol;Acc:HGNC:6719]","synonyms":"MGC33147","biotype":"protein_coding","ncbi_id":"4056","summary":"The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family includes a number of human proteins, several of which are involved the production of leukotrienes. This gene encodes an enzyme that catalyzes the first step in the biosynthesis of cysteinyl leukotrienes, potent biological compounds derived from arachidonic acid. Leukotrienes have been implicated as mediators of anaphylaxis and inflammatory conditions such as human bronchial asthma. This protein localizes to the nuclear envelope and adjacent endoplasmic reticulum. [provided by RefSeq, Jul 2008]","start":179794850,"end":179797517,"strand":1,"description":"leukotriene C4 synthase [Source:HGNC Symbol;Acc:HGNC:6719]"}, {"versioned_ensembl_gene_id":"ENSG00000284501.1","gene_symbol":"MGAT4B","gene_name":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:7048]","synonyms":"GnT-Ivb","biotype":"protein_coding","ncbi_id":"11282","summary":"This gene encodes a key glycosyltransferase that regulates the formation of tri- and multiantennary branching structures in the Golgi apparatus. The encoded protein, in addition to the related isoenzyme A, catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc in a beta-1,4 linkage to the Man-alpha-1,3-Man-beta-1,4-GlcNAc arm of R-Man-alpha-1,6(GlcNAc-beta-1,2-Man-alpha-1,3)Man-beta-1,4-GlcNAc-beta-1,4-GlcNAc-beta-1-Asn. The encoded protein may play a role in regulating the availability of serum glycoproteins, oncogenesis, and differentiation. [provided by RefSeq, Jul 2008]","start":179798463,"end":179807814,"strand":-1,"description":"mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B [Source:HGNC Symbol;Acc:HGNC:7048]"}, {"versioned_ensembl_gene_id":"ENSG00000283912.1","gene_symbol":"MIR1229","gene_name":"microRNA 1229 [Source:HGNC Symbol;Acc:HGNC:33924]","synonyms":"MIRN1229,hsa-mir-1229","biotype":"miRNA","ncbi_id":"100302156","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":179799144,"end":179799212,"strand":-1,"description":"microRNA 1229 [Source:HGNC Symbol;Acc:HGNC:33924]"}, {"versioned_ensembl_gene_id":"ENSG00000282846.1","gene_symbol":"AC008982.4","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":38844765,"end":38845535,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282895.1","gene_symbol":"RINL","gene_name":"Ras and Rab interactor like [Source:HGNC Symbol;Acc:HGNC:24795]","synonyms":"FLJ45909","biotype":"protein_coding","ncbi_id":"126432","summary":null,"start":38867870,"end":38878315,"strand":-1,"description":"Ras and Rab interactor like [Source:HGNC Symbol;Acc:HGNC:24795]"}, {"versioned_ensembl_gene_id":"ENSG00000283121.1","gene_symbol":"AC011455.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":38870195,"end":38873799,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283918.1","gene_symbol":"MRNIP","gene_name":"MRN complex interacting protein [Source:HGNC Symbol;Acc:HGNC:30817]","synonyms":"MGC78537,MGC65027,LOC51149,DKFZp686L2452,C5orf45","biotype":"protein_coding","ncbi_id":"51149","summary":null,"start":179835986,"end":179863026,"strand":-1,"description":"MRN complex interacting protein [Source:HGNC Symbol;Acc:HGNC:30817]"}, {"versioned_ensembl_gene_id":"ENSG00000283100.1","gene_symbol":"SIRT2","gene_name":"sirtuin 2 [Source:HGNC Symbol;Acc:HGNC:10886]","synonyms":"SIR2L","biotype":"protein_coding","ncbi_id":"22933","summary":"This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Several transcript variants are resulted from alternative splicing of this gene. [provided by RefSeq, Jul 2010]","start":38878591,"end":38899898,"strand":-1,"description":"sirtuin 2 [Source:HGNC Symbol;Acc:HGNC:10886]"}, {"versioned_ensembl_gene_id":"ENSG00000284026.1","gene_symbol":"RN7SKP150","gene_name":"RNA, 7SK small nuclear pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:45874]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480880","summary":null,"start":179846685,"end":179847005,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 150 [Source:HGNC Symbol;Acc:HGNC:45874]"}, {"versioned_ensembl_gene_id":"ENSG00000284437.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":179847888,"end":179847983,"strand":-1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000284274.1","gene_symbol":"AC008393.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":179859866,"end":179862136,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284400.1","gene_symbol":"TBC1D9B","gene_name":"TBC1 domain family member 9B [Source:HGNC Symbol;Acc:HGNC:29097]","synonyms":"KIAA0676,GRAMD9B","biotype":"protein_coding","ncbi_id":"23061","summary":null,"start":179862919,"end":179908712,"strand":-1,"description":"TBC1 domain family member 9B [Source:HGNC Symbol;Acc:HGNC:29097]"}, {"versioned_ensembl_gene_id":"ENSG00000283557.2","gene_symbol":"AC244647.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21667851,"end":21668791,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283854.1","gene_symbol":"AC244647.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21669138,"end":21670803,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284529.1","gene_symbol":"AC244647.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21743762,"end":21743868,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282905.1","gene_symbol":"NFKBIB","gene_name":"NFKB inhibitor beta [Source:HGNC Symbol;Acc:HGNC:7798]","synonyms":"TRIP9,IKBB","biotype":"protein_coding","ncbi_id":"4793","summary":"The protein encoded by this gene belongs to the NF-kappa-B inhibitor family, which inhibit NF-kappa-B by complexing with, and trapping it in the cytoplasm. Phosphorylation of serine residues on these proteins by kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation of the NF-kappa-B, which translocates to the nucleus to function as a transcription factor. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jul 2011]","start":38899736,"end":38908929,"strand":1,"description":"NFKB inhibitor beta [Source:HGNC Symbol;Acc:HGNC:7798]"}, {"versioned_ensembl_gene_id":"ENSG00000283099.1","gene_symbol":"CCER2","gene_name":"coiled-coil glutamate rich protein 2 [Source:HGNC Symbol;Acc:HGNC:44662]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643669","summary":null,"start":38909016,"end":38912194,"strand":-1,"description":"coiled-coil glutamate rich protein 2 [Source:HGNC Symbol;Acc:HGNC:44662]"}, {"versioned_ensembl_gene_id":"ENSG00000283104.1","gene_symbol":"SARS2","gene_name":"seryl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17697]","synonyms":"FLJ20450,SYS,SERS,SerRSmt,SARSM,SARS,mtSerRS","biotype":"protein_coding","ncbi_id":"54938","summary":"This gene encodes the mitochondrial seryl-tRNA synthethase precursor, a member of the class II tRNA synthetase family. The mature enzyme catalyzes the ligation of Serine to tRNA(Ser) and participates in the biosynthesis of selenocysteinyl-tRNA(sec) in mitochondria. The enzyme contains an N-terminal tRNA binding domain and a core catalytic domain. It functions in a homodimeric form, which is stabilized by tRNA binding. This gene is regulated by a bidirectional promoter that also controls the expression of mitochondrial ribosomal protein S12. Both genes are within the critical interval for the autosomal dominant deafness locus DFNA4 and might be linked to this disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Mar 2009]","start":38915302,"end":38930932,"strand":-1,"description":"seryl-tRNA synthetase 2, mitochondrial [Source:HGNC Symbol;Acc:HGNC:17697]"}, {"versioned_ensembl_gene_id":"ENSG00000284254.1","gene_symbol":"AC270306.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":179616411,"end":179624701,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282835.1","gene_symbol":"AC011455.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":38915440,"end":38949891,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284445.1","gene_symbol":"AC270227.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":179649036,"end":179651563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284099.1","gene_symbol":"AC008393.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":179821790,"end":179837507,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283018.1","gene_symbol":"MRPS12","gene_name":"mitochondrial ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10380]","synonyms":"RPSM12,RPS12,RPMS12","biotype":"protein_coding","ncbi_id":"6183","summary":"Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that belongs to the ribosomal protein S12P family. The encoded protein is a key component of the ribosomal small subunit and controls the decoding fidelity and susceptibility to aminoglycoside antibiotics. The gene for mitochondrial seryl-tRNA synthetase is located upstream and adjacent to this gene, and both genes are possible candidates for the autosomal dominant deafness gene (DFNA4). Splice variants that differ in the 5' UTR have been found for this gene; all three variants encode the same protein. [provided by RefSeq, Jul 2008]","start":38930584,"end":38933198,"strand":1,"description":"mitochondrial ribosomal protein S12 [Source:HGNC Symbol;Acc:HGNC:10380]"}, {"versioned_ensembl_gene_id":"ENSG00000282930.1","gene_symbol":"AC011455.5","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":38935333,"end":38938668,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282954.1","gene_symbol":"FBXO17","gene_name":"F-box protein 17 [Source:HGNC Symbol;Acc:HGNC:18754]","synonyms":"MGC9379,FLJ25205,FLJ11798,FBXO26,Fbx17,FBG4","biotype":"protein_coding","ncbi_id":"115290","summary":"This gene encodes a member of the F-box protein family which is characterized by the F-box motif. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it contains an F-box domain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","start":38941437,"end":38975946,"strand":-1,"description":"F-box protein 17 [Source:HGNC Symbol;Acc:HGNC:18754]"}, {"versioned_ensembl_gene_id":"ENSG00000283021.1","gene_symbol":"FBXO27","gene_name":"F-box protein 27 [Source:HGNC Symbol;Acc:HGNC:18753]","synonyms":"Fbx27,Fbg5","biotype":"protein_coding","ncbi_id":"126433","summary":"Members of the F-box protein family, such as FBXO27, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]","start":38990750,"end":39032821,"strand":-1,"description":"F-box protein 27 [Source:HGNC Symbol;Acc:HGNC:18753]"}, {"versioned_ensembl_gene_id":"ENSG00000284255.1","gene_symbol":"OR4C12","gene_name":"olfactory receptor family 4 subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:15168]","synonyms":null,"biotype":"protein_coding","ncbi_id":"283093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":49981473,"end":49982535,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 12 [Source:HGNC Symbol;Acc:HGNC:15168]"}, {"versioned_ensembl_gene_id":"ENSG00000284278.1","gene_symbol":"AC110057.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":50018798,"end":50019695,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284123.1","gene_symbol":"OR4C49P","gene_name":"olfactory receptor family 4 subfamily C member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31273]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"403260","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":50053408,"end":50054307,"strand":-1,"description":"olfactory receptor family 4 subfamily C member 49 pseudogene [Source:HGNC Symbol;Acc:HGNC:31273]"}, {"versioned_ensembl_gene_id":"ENSG00000284189.1","gene_symbol":"AC141424.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":404468,"end":414023,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281198.1","gene_symbol":"AC208067.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":21196720,"end":21196860,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283838.1","gene_symbol":"AC140172.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":21109383,"end":21110489,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283781.1","gene_symbol":"TNK1","gene_name":"tyrosine kinase non receptor 1 [Source:HGNC Symbol;Acc:HGNC:11940]","synonyms":null,"biotype":"protein_coding","ncbi_id":"8711","summary":"The protein encoded by this gene belongs to the tyrosine protein kinase family. Tyrosine protein kinases are important regulators of intracellular signal transduction pathways, mediating cellular proliferation, survival, and development. This gene is highly expressed in fetal tissues and at lower levels in few adult tissues, thus may function in signaling pathways utilized broadly during fetal development, and more selectively in adult tissues. It plays a negative regulatory role in the Ras-Raf1-MAPK pathway, and knockout mice have been shown to develop spontaneous tumors, suggesting a role as a tumor suppressor gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]","start":7380534,"end":7389774,"strand":1,"description":"tyrosine kinase non receptor 1 [Source:HGNC Symbol;Acc:HGNC:11940]"}, {"versioned_ensembl_gene_id":"ENSG00000283985.1","gene_symbol":"C17orf97","gene_name":"chromosome 17 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:33800]","synonyms":"LOC400566,LIAT1","biotype":"protein_coding","ncbi_id":"400566","summary":null,"start":410327,"end":431062,"strand":1,"description":"chromosome 17 open reading frame 97 [Source:HGNC Symbol;Acc:HGNC:33800]"}, {"versioned_ensembl_gene_id":"ENSG00000284367.1","gene_symbol":"LINC01606","gene_name":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]","synonyms":"TCONS_l2_00027778","biotype":"lincRNA","ncbi_id":"100507651","summary":null,"start":57148487,"end":57246096,"strand":1,"description":"long intergenic non-protein coding RNA 1606 [Source:HGNC Symbol;Acc:HGNC:51656]"}, {"versioned_ensembl_gene_id":"ENSG00000283007.1","gene_symbol":"AC021427.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":7704628,"end":7893073,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282971.1","gene_symbol":"AC044810.7","gene_name":null,"synonyms":null,"biotype":"sense_overlapping","ncbi_id":null,"summary":null,"start":7754393,"end":7916081,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283979.1","gene_symbol":"RFLNB","gene_name":"refilin B [Source:HGNC Symbol;Acc:HGNC:28705]","synonyms":"FAM101B,Cfm1,RefilinB,MGC45871","biotype":"protein_coding","ncbi_id":"359845","summary":null,"start":439978,"end":445939,"strand":-1,"description":"refilin B [Source:HGNC Symbol;Acc:HGNC:28705]"}, {"versioned_ensembl_gene_id":"ENSG00000281118.1","gene_symbol":"AC044810.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":7783697,"end":7784407,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284165.1","gene_symbol":"AC015853.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":465285,"end":473461,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280931.1","gene_symbol":"OR5P2","gene_name":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]","synonyms":"JCG3","biotype":"protein_coding","ncbi_id":"120065","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7795905,"end":7796973,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 2 [Source:HGNC Symbol;Acc:HGNC:14783]"}, {"versioned_ensembl_gene_id":"ENSG00000280808.2","gene_symbol":"OR5P3","gene_name":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]","synonyms":"JCG1","biotype":"protein_coding","ncbi_id":"120066","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7834940,"end":7840960,"strand":-1,"description":"olfactory receptor family 5 subfamily P member 3 [Source:HGNC Symbol;Acc:HGNC:14784]"}, {"versioned_ensembl_gene_id":"ENSG00000281056.1","gene_symbol":"OR5E1P","gene_name":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]","synonyms":"TPCR24,OR5E1,HSTPCR24","biotype":"unprocessed_pseudogene","ncbi_id":"26343","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7858826,"end":7859752,"strand":1,"description":"olfactory receptor family 5 subfamily E member 1 pseudogene [Source:HGNC Symbol;Acc:HGNC:8342]"}, {"versioned_ensembl_gene_id":"ENSG00000281563.1","gene_symbol":"RNU6-943P","gene_name":"RNA, U6 small nuclear 943, pseudogene [Source:HGNC Symbol;Acc:HGNC:47906]","synonyms":null,"biotype":"snRNA","ncbi_id":"106480623","summary":null,"start":7899308,"end":7899405,"strand":-1,"description":"RNA, U6 small nuclear 943, pseudogene [Source:HGNC Symbol;Acc:HGNC:47906]"}, {"versioned_ensembl_gene_id":"ENSG00000280899.3","gene_symbol":"OR10A6","gene_name":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]","synonyms":null,"biotype":"polymorphic_pseudogene","ncbi_id":"390093","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015]","start":7934718,"end":7941394,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:15132]"}, {"versioned_ensembl_gene_id":"ENSG00000281680.2","gene_symbol":"OR10A3","gene_name":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]","synonyms":"HTPCRX12,HSHTPCRX12","biotype":"protein_coding","ncbi_id":"26496","summary":"Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]","start":7947297,"end":7951834,"strand":-1,"description":"olfactory receptor family 10 subfamily A member 3 [Source:HGNC Symbol;Acc:HGNC:8162]"}, {"versioned_ensembl_gene_id":"ENSG00000283997.1","gene_symbol":"TMEM159","gene_name":"transmembrane protein 159 [Source:HGNC Symbol;Acc:HGNC:30136]","synonyms":"promethin","biotype":"protein_coding","ncbi_id":"57146","summary":null,"start":21158377,"end":21180616,"strand":1,"description":"transmembrane protein 159 [Source:HGNC Symbol;Acc:HGNC:30136]"}, {"versioned_ensembl_gene_id":"ENSG00000283987.1","gene_symbol":"RRN3P3","gene_name":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37620]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100131998","summary":null,"start":21843633,"end":21862676,"strand":1,"description":"RRN3 homolog, RNA polymerase I transcription factor pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:37620]"}, {"versioned_ensembl_gene_id":"ENSG00000281166.1","gene_symbol":"NLRP10","gene_name":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]","synonyms":"Pynod,PAN5,NOD8,NALP10,CLR11.1","biotype":"protein_coding","ncbi_id":"338322","summary":"Members of the NALP protein family typically contain a NACHT domain, a NACHT-associated domain (NAD), a C-terminal leucine-rich repeat (LRR) region, and an N-terminal pyrin domain (PYD). The protein encoded by this gene belongs to the NALP protein family despite lacking the LRR region. This protein likely plays a regulatory role in the innate immune system. The protein belongs to the signal-induced multiprotein complex, the inflammasome, that activates the pro-inflammatory caspases, caspase-1 and caspase-5. Other experiments indicate that this gene acts as a multifunctional negative regulator of inflammation and apoptosis. [provided by RefSeq, Jul 2008]","start":7969550,"end":7975552,"strand":-1,"description":"NLR family pyrin domain containing 10 [Source:HGNC Symbol;Acc:HGNC:21464]"}, {"versioned_ensembl_gene_id":"ENSG00000280606.3","gene_symbol":"EIF3F","gene_name":"eukaryotic translation initiation factor 3 subunit F [Source:HGNC Symbol;Acc:HGNC:3275]","synonyms":"eIF3-epsilon,EIF3S5,eIF3f,eIF3-p47","biotype":"protein_coding","ncbi_id":"8665","summary":null,"start":7980377,"end":8011988,"strand":1,"description":"eukaryotic translation initiation factor 3 subunit F [Source:HGNC Symbol;Acc:HGNC:3275]"}, {"versioned_ensembl_gene_id":"ENSG00000284009.1","gene_symbol":"PLSCR3","gene_name":"phospholipid scramblase 3 [Source:HGNC Symbol;Acc:HGNC:16495]","synonyms":null,"biotype":"protein_coding","ncbi_id":"57048","summary":null,"start":7389727,"end":7394843,"strand":-1,"description":"phospholipid scramblase 3 [Source:HGNC Symbol;Acc:HGNC:16495]"}, {"versioned_ensembl_gene_id":"ENSG00000284382.1","gene_symbol":"AF001550.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21194847,"end":21205977,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284476.1","gene_symbol":"AC044810.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7784186,"end":7784434,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284056.1","gene_symbol":"AC243812.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":7823123,"end":7823348,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284569.1","gene_symbol":"AC044810.9","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":7926284,"end":7927676,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284597.1","gene_symbol":"AC044810.10","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":7931256,"end":7931985,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283883.1","gene_symbol":"VPS53","gene_name":"VPS53, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:25608]","synonyms":"HCCS1,FLJ10979","biotype":"protein_coding","ncbi_id":"55275","summary":"This gene encodes a protein with sequence similarity to the yeast Vps53p protein. Vps53p is involved in retrograde vesicle trafficking in late Golgi. [provided by RefSeq, Jul 2008]","start":470782,"end":683831,"strand":-1,"description":"VPS53, GARP complex subunit [Source:HGNC Symbol;Acc:HGNC:25608]"}, {"versioned_ensembl_gene_id":"ENSG00000284588.1","gene_symbol":"ZP2","gene_name":"zona pellucida glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:13188]","synonyms":"ZPA","biotype":"protein_coding","ncbi_id":"7783","summary":"The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed of three glycoproteins with various functions during fertilization and preimplantation development. The glycosylated mature peptide is one of the structural components of the zona pellucida and functions in secondary binding and penetration of acrosome-reacted spermatozoa. Female mice lacking this gene do not form a stable zona matrix and are sterile. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]","start":21197450,"end":21214510,"strand":-1,"description":"zona pellucida glycoprotein 2 [Source:HGNC Symbol;Acc:HGNC:13188]"}, {"versioned_ensembl_gene_id":"ENSG00000284290.1","gene_symbol":"ANKS4B","gene_name":"ankyrin repeat and sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:26795]","synonyms":"HARP,FLJ38819","biotype":"protein_coding","ncbi_id":"257629","summary":null,"start":21233665,"end":21253845,"strand":1,"description":"ankyrin repeat and sterile alpha motif domain containing 4B [Source:HGNC Symbol;Acc:HGNC:26795]"}, {"versioned_ensembl_gene_id":"ENSG00000284483.1","gene_symbol":"TMEM256-PLSCR3","gene_name":"TMEM256-PLSCR3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49186]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100529211","summary":"This locus represents naturally occurring read-through transcription between the neighboring chromosome 17 open reading frame 61 (C17orf61) and phospholipid scramblase 3 (PLSCR3) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Jan 2011]","start":7389734,"end":7404097,"strand":-1,"description":"TMEM256-PLSCR3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49186]"}, {"versioned_ensembl_gene_id":"ENSG00000283922.1","gene_symbol":"CRYM","gene_name":"crystallin mu [Source:HGNC Symbol;Acc:HGNC:2418]","synonyms":"DFNA40","biotype":"protein_coding","ncbi_id":"1428","summary":"Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness. [provided by RefSeq, Sep 2014]","start":21238874,"end":21303084,"strand":-1,"description":"crystallin mu [Source:HGNC Symbol;Acc:HGNC:2418]"}, {"versioned_ensembl_gene_id":"ENSG00000283771.1","gene_symbol":"TMEM256","gene_name":"transmembrane protein 256 [Source:HGNC Symbol;Acc:HGNC:28618]","synonyms":"MGC40107,C17orf61","biotype":"protein_coding","ncbi_id":"254863","summary":null,"start":7402975,"end":7404137,"strand":-1,"description":"transmembrane protein 256 [Source:HGNC Symbol;Acc:HGNC:28618]"}, {"versioned_ensembl_gene_id":"ENSG00000283859.1","gene_symbol":"NLGN2","gene_name":"neuroligin 2 [Source:HGNC Symbol;Acc:HGNC:14290]","synonyms":"KIAA1366","biotype":"protein_coding","ncbi_id":"57555","summary":"This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. [provided by RefSeq, Jul 2008]","start":7404874,"end":7419860,"strand":1,"description":"neuroligin 2 [Source:HGNC Symbol;Acc:HGNC:14290]"}, {"versioned_ensembl_gene_id":"ENSG00000283843.1","gene_symbol":"AC113189.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":7420103,"end":7444081,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284598.1","gene_symbol":"SPEM1","gene_name":"spermatid maturation 1 [Source:HGNC Symbol;Acc:HGNC:32429]","synonyms":"FLJ40081,C17orf83","biotype":"protein_coding","ncbi_id":"374768","summary":null,"start":7420360,"end":7421632,"strand":1,"description":"spermatid maturation 1 [Source:HGNC Symbol;Acc:HGNC:32429]"}, {"versioned_ensembl_gene_id":"ENSG00000284404.1","gene_symbol":"AC241640.6","gene_name":null,"synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":null,"summary":null,"start":21299903,"end":21300506,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283817.1","gene_symbol":"AC241640.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21347129,"end":21352128,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284359.1","gene_symbol":"AC241640.5","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":21401067,"end":21401176,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283714.1","gene_symbol":"C17orf74","gene_name":"chromosome 17 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27315]","synonyms":null,"biotype":"protein_coding","ncbi_id":"201243","summary":null,"start":7425615,"end":7427568,"strand":1,"description":"chromosome 17 open reading frame 74 [Source:HGNC Symbol;Acc:HGNC:27315]"}, {"versioned_ensembl_gene_id":"ENSG00000284090.1","gene_symbol":"AC113189.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7428903,"end":7432762,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284578.1","gene_symbol":"SMG1P1","gene_name":"SMG1P1, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44186]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"641298","summary":null,"start":21445752,"end":21844340,"strand":-1,"description":"SMG1P1, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:44186]"}, {"versioned_ensembl_gene_id":"ENSG00000284228.1","gene_symbol":"TMEM102","gene_name":"transmembrane protein 102 [Source:HGNC Symbol;Acc:HGNC:26722]","synonyms":"FLJ36878,CBAP","biotype":"protein_coding","ncbi_id":"284114","summary":null,"start":7435443,"end":7437679,"strand":1,"description":"transmembrane protein 102 [Source:HGNC Symbol;Acc:HGNC:26722]"}, {"versioned_ensembl_gene_id":"ENSG00000283895.1","gene_symbol":"AC113189.8","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":7436557,"end":7437523,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283903.1","gene_symbol":"FGF11","gene_name":"fibroblast growth factor 11 [Source:HGNC Symbol;Acc:HGNC:3667]","synonyms":"MGC45269,MGC102953,FLJ16061,FHF3","biotype":"protein_coding","ncbi_id":"2256","summary":"The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The function of this gene has not yet been determined. The expression pattern of the mouse homolog implies a role in nervous system development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]","start":7438273,"end":7444937,"strand":1,"description":"fibroblast growth factor 11 [Source:HGNC Symbol;Acc:HGNC:3667]"}, {"versioned_ensembl_gene_id":"ENSG00000283814.1","gene_symbol":"MFSD13B","gene_name":"major facilitator superfamily domain containing 13B [Source:HGNC Symbol;Acc:HGNC:52163]","synonyms":null,"biotype":"unitary_pseudogene","ncbi_id":"105371130","summary":null,"start":21873920,"end":21898912,"strand":-1,"description":"major facilitator superfamily domain containing 13B [Source:HGNC Symbol;Acc:HGNC:52163]"}, {"versioned_ensembl_gene_id":"ENSG00000284019.1","gene_symbol":"AC241556.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21903168,"end":21906489,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283831.1","gene_symbol":"AC241556.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21912295,"end":21916221,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283946.1","gene_symbol":"CHRNB1","gene_name":"cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961]","synonyms":"CHRNB","biotype":"protein_coding","ncbi_id":"1140","summary":"The muscle acetylcholine receptor is composed of five subunits: two alpha subunits and one beta, one gamma, and one delta subunit. This gene encodes the beta subunit of the acetylcholine receptor. The acetylcholine receptor changes conformation upon acetylcholine binding leading to the opening of an ion-conducting channel across the plasma membrane. Mutations in this gene are associated with slow-channel congenital myasthenic syndrome. [provided by RefSeq, Jul 2008]","start":7445061,"end":7457707,"strand":1,"description":"cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961]"}, {"versioned_ensembl_gene_id":"ENSG00000284075.1","gene_symbol":"AC015853.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":485254,"end":502690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284323.1","gene_symbol":"AC015853.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":514680,"end":515531,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284390.1","gene_symbol":"AC027455.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":578116,"end":578709,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284153.1","gene_symbol":"RPS4XP17","gene_name":"ribosomal protein S4X pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36789]","synonyms":"RPS4P17","biotype":"processed_pseudogene","ncbi_id":"100128140","summary":null,"start":618908,"end":619661,"strand":-1,"description":"ribosomal protein S4X pseudogene 17 [Source:HGNC Symbol;Acc:HGNC:36789]"}, {"versioned_ensembl_gene_id":"ENSG00000284282.1","gene_symbol":"POLR3E","gene_name":"RNA polymerase III subunit E [Source:HGNC Symbol;Acc:HGNC:30347]","synonyms":"SIN,RPC5,FLJ10509","biotype":"protein_coding","ncbi_id":"55718","summary":null,"start":21946236,"end":21983964,"strand":-1,"description":"RNA polymerase III subunit E [Source:HGNC Symbol;Acc:HGNC:30347]"}, {"versioned_ensembl_gene_id":"ENSG00000283868.1","gene_symbol":"ZBTB4","gene_name":"zinc finger and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23847]","synonyms":"KIAA1538,KAISO-L1,ZNF903","biotype":"protein_coding","ncbi_id":"57659","summary":null,"start":7459366,"end":7484263,"strand":-1,"description":"zinc finger and BTB domain containing 4 [Source:HGNC Symbol;Acc:HGNC:23847]"}, {"versioned_ensembl_gene_id":"ENSG00000284515.1","gene_symbol":"SLC35G6","gene_name":"solute carrier family 35 member G6 [Source:HGNC Symbol;Acc:HGNC:31351]","synonyms":"TMEM21B,AMAC1L3","biotype":"protein_coding","ncbi_id":"643664","summary":null,"start":7481332,"end":7483496,"strand":1,"description":"solute carrier family 35 member G6 [Source:HGNC Symbol;Acc:HGNC:31351]"}, {"versioned_ensembl_gene_id":"ENSG00000279335.2","gene_symbol":"AC113189.5","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":7433380,"end":7433566,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284187.1","gene_symbol":"KF459570.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":7496797,"end":7497123,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284521.1","gene_symbol":"AC241556.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21992621,"end":21994650,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284349.1","gene_symbol":"SDR42E2","gene_name":"short chain dehydrogenase/reductase family 42E, member 2 [Source:HGNC Symbol;Acc:HGNC:35414]","synonyms":null,"biotype":"protein_coding","ncbi_id":"100288072","summary":null,"start":22089594,"end":22115764,"strand":-1,"description":"short chain dehydrogenase/reductase family 42E, member 2 [Source:HGNC Symbol;Acc:HGNC:35414]"}, {"versioned_ensembl_gene_id":"ENSG00000283835.1","gene_symbol":"VWA3A","gene_name":"von Willebrand factor A domain containing 3A [Source:HGNC Symbol;Acc:HGNC:27088]","synonyms":"FLJ46765,FLJ40941","biotype":"protein_coding","ncbi_id":"146177","summary":null,"start":22124381,"end":22188809,"strand":-1,"description":"von Willebrand factor A domain containing 3A [Source:HGNC Symbol;Acc:HGNC:27088]"}, {"versioned_ensembl_gene_id":"ENSG00000284366.1","gene_symbol":"AC243828.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22189116,"end":22198091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284487.1","gene_symbol":"C16orf52","gene_name":"chromosome 16 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:27087]","synonyms":null,"biotype":"protein_coding","ncbi_id":"730094","summary":null,"start":22193813,"end":22273709,"strand":-1,"description":"chromosome 16 open reading frame 52 [Source:HGNC Symbol;Acc:HGNC:27087]"}, {"versioned_ensembl_gene_id":"ENSG00000283816.1","gene_symbol":"AC275435.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":22273285,"end":22273867,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284316.1","gene_symbol":"PDZD9","gene_name":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]","synonyms":"MGC50721,C16orf65","biotype":"protein_coding","ncbi_id":"255762","summary":null,"start":22280238,"end":22297482,"strand":1,"description":"PDZ domain containing 9 [Source:HGNC Symbol;Acc:HGNC:28740]"}, {"versioned_ensembl_gene_id":"ENSG00000284243.1","gene_symbol":"AC275435.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22281692,"end":22283038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284493.1","gene_symbol":"UQCRC2","gene_name":"ubiquinol-cytochrome c reductase core protein II [Source:HGNC Symbol;Acc:HGNC:12586]","synonyms":"UQCR2,QCR2","biotype":"protein_coding","ncbi_id":"7385","summary":"The protein encoded by this gene is located in the mitochondrion, where it is part of the ubiquinol-cytochrome c reductase complex (also known as complex III). This complex constitutes a part of the mitochondrial respiratory chain. Defects in this gene are a cause of mitochondrial complex III deficiency nuclear type 5. [provided by RefSeq, Jul 2015]","start":22297687,"end":22328688,"strand":-1,"description":"ubiquinol-cytochrome c reductase core protein II [Source:HGNC Symbol;Acc:HGNC:12586]"}, {"versioned_ensembl_gene_id":"ENSG00000284270.1","gene_symbol":"AC241401.3","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":22329640,"end":22331130,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283943.1","gene_symbol":"AC241401.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22336362,"end":22342484,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283826.1","gene_symbol":"SMG1P4","gene_name":"SMG1P4, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49861]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100507526","summary":null,"start":22362191,"end":22402009,"strand":1,"description":"SMG1P4, nonsense mediated mRNA decay associated PI3K related kinase pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49861]"}, {"versioned_ensembl_gene_id":"ENSG00000283908.1","gene_symbol":"AC241988.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":22447463,"end":22447568,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284170.1","gene_symbol":"AC241988.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":22485330,"end":22486994,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284548.1","gene_symbol":"METTL9","gene_name":"methyltransferase like 9 [Source:HGNC Symbol;Acc:HGNC:24586]","synonyms":"DREV1","biotype":"protein_coding","ncbi_id":"51108","summary":null,"start":22623664,"end":22683908,"strand":-1,"description":"methyltransferase like 9 [Source:HGNC Symbol;Acc:HGNC:24586]"}, {"versioned_ensembl_gene_id":"ENSG00000283934.1","gene_symbol":"IGSF6","gene_name":"immunoglobulin superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:5953]","synonyms":"DORA","biotype":"protein_coding","ncbi_id":"10261","summary":null,"start":22628477,"end":22641600,"strand":1,"description":"immunoglobulin superfamily member 6 [Source:HGNC Symbol;Acc:HGNC:5953]"}, {"versioned_ensembl_gene_id":"ENSG00000284403.1","gene_symbol":"RNU6-196P","gene_name":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481238","summary":null,"start":22638737,"end":22638843,"strand":-1,"description":"RNA, U6 small nuclear 196, pseudogene [Source:HGNC Symbol;Acc:HGNC:47159]"}, {"versioned_ensembl_gene_id":"ENSG00000283754.1","gene_symbol":"RNU6-1005P","gene_name":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]","synonyms":null,"biotype":"snRNA","ncbi_id":"106481497","summary":null,"start":22638977,"end":22639083,"strand":-1,"description":"RNA, U6 small nuclear 1005, pseudogene [Source:HGNC Symbol;Acc:HGNC:47968]"}, {"versioned_ensembl_gene_id":"ENSG00000284429.1","gene_symbol":"AC241409.1","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":22653567,"end":22654394,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284083.1","gene_symbol":"SCARNA6","gene_name":"Small Cajal body specific RNA 6 [Source:RFAM;Acc:RF00478]","synonyms":"U88","biotype":"scaRNA","ncbi_id":"677772","summary":null,"start":22693262,"end":22693499,"strand":-1,"description":"Small Cajal body specific RNA 6 [Source:RFAM;Acc:RF00478]"}, {"versioned_ensembl_gene_id":"ENSG00000284023.1","gene_symbol":"SLC7A5P2","gene_name":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]","synonyms":"IMAA,hLAT1-3TM","biotype":"transcribed_processed_pseudogene","ncbi_id":"387254","summary":null,"start":22760761,"end":22761296,"strand":1,"description":"solute carrier family 7 member 5 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:24951]"}, {"versioned_ensembl_gene_id":"ENSG00000280467.2","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42147866,"end":42331469,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000282009.1","gene_symbol":"RNU6-17P","gene_name":"RNA, U6 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:34261]","synonyms":"RNU6-17","biotype":"snRNA","ncbi_id":"106480705","summary":null,"start":30255704,"end":30255810,"strand":-1,"description":"RNA, U6 small nuclear 17, pseudogene [Source:HGNC Symbol;Acc:HGNC:34261]"}, {"versioned_ensembl_gene_id":"ENSG00000282722.1","gene_symbol":"AC254958.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":30353939,"end":30357863,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284352.1","gene_symbol":"MIR3680-1","gene_name":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]","synonyms":"MIR3680,hsa-mir-3680","biotype":"miRNA","ncbi_id":"100500917","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":22774987,"end":22775073,"strand":1,"description":"microRNA 3680-1 [Source:HGNC Symbol;Acc:HGNC:38989]"}, {"versioned_ensembl_gene_id":"ENSG00000283738.1","gene_symbol":"AC241640.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21404361,"end":21424167,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283786.1","gene_symbol":"AC241640.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21454850,"end":21459206,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283892.1","gene_symbol":"AC241640.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21472115,"end":21500657,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284218.1","gene_symbol":"AC241410.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21744964,"end":21767544,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284077.1","gene_symbol":"AC241556.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21916402,"end":21933866,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284161.1","gene_symbol":"AC241556.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21997365,"end":22055624,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283855.1","gene_symbol":"AC241401.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22423969,"end":22446363,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284559.1","gene_symbol":"AC241409.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22520552,"end":22559704,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284330.1","gene_symbol":"AC256236.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22779238,"end":22808047,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283711.1","gene_symbol":"AC256236.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22820947,"end":22825311,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284454.1","gene_symbol":"AC256236.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":22855983,"end":22878913,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283102.1","gene_symbol":"AC111152.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":30005443,"end":30045854,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283119.1","gene_symbol":"AC205875.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":103926563,"end":103927802,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282193.1","gene_symbol":"AC254979.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30044461,"end":30045302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281013.2","gene_symbol":"NDUFA6","gene_name":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]","synonyms":"LYRM6,CI-B14,B14,NADHB14","biotype":"protein_coding","ncbi_id":"4700","summary":"This gene encodes a member of the LYR family of proteins that contain a highly conserved tripeptide (LYR) motif near the N-terminus. The encoded protein is an accessory subunit of NADH: ubiquinone oxidorerductase (Complex I), which is the largest enzyme of the mitochondrial membrane respiratory chain. Complex I functions in electron transfer from NADH to the respiratory chain. [provided by RefSeq, Oct 2016]","start":42085525,"end":42090965,"strand":-1,"description":"NADH:ubiquinone oxidoreductase subunit A6 [Source:HGNC Symbol;Acc:HGNC:7690]"}, {"versioned_ensembl_gene_id":"ENSG00000282362.2","gene_symbol":"AC254979.2","gene_name":null,"synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30052948,"end":30073074,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282654.1","gene_symbol":"RN7SL673P","gene_name":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480525","summary":null,"start":30091657,"end":30091893,"strand":1,"description":"RNA, 7SL, cytoplasmic 673, pseudogene [Source:HGNC Symbol;Acc:HGNC:46689]"}, {"versioned_ensembl_gene_id":"ENSG00000282324.1","gene_symbol":"DNM1P28","gene_name":"dynamin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35175]","synonyms":"DNM1DN3-1,DNM1DN3@,DNM1DN3-3","biotype":"unprocessed_pseudogene","ncbi_id":"100132031","summary":null,"start":30098819,"end":30102086,"strand":-1,"description":"dynamin 1 pseudogene 28 [Source:HGNC Symbol;Acc:HGNC:35175]"}, {"versioned_ensembl_gene_id":"ENSG00000282509.1","gene_symbol":"ULK4P3","gene_name":"ULK4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:15777]","synonyms":"FAM7A3,D-X","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"89837","summary":null,"start":30103719,"end":30131750,"strand":1,"description":"ULK4 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:15777]"}, {"versioned_ensembl_gene_id":"ENSG00000283030.1","gene_symbol":"CSN2","gene_name":"casein beta [Source:HGNC Symbol;Acc:HGNC:2447]","synonyms":"CASB","biotype":"protein_coding","ncbi_id":"1447","summary":"This gene is a member of the beta casein family. There are two types of casein protein, beta (encoded by this gene) and kappa, both of which are secreted in human milk. Beta casein is the principal protein in human milk and the primary source of essential amino acids for a suckling infant. Beta and kappa casein proteins acting together form spherical micelles which bind within them important dietary minerals, such as calcium and phosphorous. In addition, the C-terminal 14 aa of the protein has antimicrobial activity, especially in preterm milk, displaying antibacterial activity against S. aureus and Y. enterocolitica. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2020]","start":69955256,"end":69961007,"strand":-1,"description":"casein beta [Source:HGNC Symbol;Acc:HGNC:2447]"}, {"versioned_ensembl_gene_id":"ENSG00000281750.1","gene_symbol":"AC213220.2","gene_name":null,"synonyms":null,"biotype":"sense_intronic","ncbi_id":null,"summary":null,"start":42089640,"end":42090038,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280714.1","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107776,"end":42108964,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000280705.1","gene_symbol":"AC213220.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42124292,"end":42127786,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282962.1","gene_symbol":"CPEB2-AS1","gene_name":"CPEB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49082]","synonyms":null,"biotype":"lincRNA","ncbi_id":"441009","summary":null,"start":14909961,"end":15005388,"strand":-1,"description":"CPEB2 antisense RNA 1 (head to head) [Source:HGNC Symbol;Acc:HGNC:49082]"}, {"versioned_ensembl_gene_id":"ENSG00000283109.1","gene_symbol":"AC116049.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66002771,"end":66153937,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282934.1","gene_symbol":"AL109936.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23244765,"end":23245224,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281908.1","gene_symbol":"AC213220.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42125919,"end":42127585,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282856.1","gene_symbol":"AL357556.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235361153,"end":235362540,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282938.1","gene_symbol":"AC096721.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":66007206,"end":66020717,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282767.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":30112190,"end":30112322,"strand":1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000283124.1","gene_symbol":"LINC01355","gene_name":"long intergenic non-protein coding RNA 1355 [Source:HGNC Symbol;Acc:HGNC:50584]","synonyms":null,"biotype":"lincRNA","ncbi_id":"100996511","summary":null,"start":23288773,"end":23294216,"strand":-1,"description":"long intergenic non-protein coding RNA 1355 [Source:HGNC Symbol;Acc:HGNC:50584]"}, {"versioned_ensembl_gene_id":"ENSG00000281004.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42137724,"end":42142854,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000282328.1","gene_symbol":"RN7SL469P","gene_name":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480512","summary":null,"start":30143737,"end":30143973,"strand":1,"description":"RNA, 7SL, cytoplasmic 469, pseudogene [Source:HGNC Symbol;Acc:HGNC:46485]"}, {"versioned_ensembl_gene_id":"ENSG00000282400.1","gene_symbol":"DNM1P30","gene_name":"dynamin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35177]","synonyms":"DNM1DN4@,DNM1DN4-3,DNM1DN3@,DNM1DN3-4","biotype":"unprocessed_pseudogene","ncbi_id":"728388","summary":null,"start":30150880,"end":30153410,"strand":-1,"description":"dynamin 1 pseudogene 30 [Source:HGNC Symbol;Acc:HGNC:35177]"}, {"versioned_ensembl_gene_id":"ENSG00000284647.1","gene_symbol":"AL109936.7","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23305261,"end":23310330,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282316.1","gene_symbol":"AC254962.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":30153934,"end":30154111,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282096.1","gene_symbol":"LINC02249","gene_name":"long intergenic non-protein coding RNA 2249 [Source:HGNC Symbol;Acc:HGNC:32351]","synonyms":"DKFZp434L187","biotype":"lincRNA","ncbi_id":"26082","summary":null,"start":30197311,"end":30215822,"strand":1,"description":"long intergenic non-protein coding RNA 2249 [Source:HGNC Symbol;Acc:HGNC:32351]"}, {"versioned_ensembl_gene_id":"ENSG00000282249.1","gene_symbol":"AC254962.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":30224299,"end":30226846,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282729.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":30365063,"end":30365167,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000282833.2","gene_symbol":"PHACTR1","gene_name":"phosphatase and actin regulator 1 [Source:HGNC Symbol;Acc:HGNC:20990]","synonyms":"RPEL1,KIAA1733,dJ257A7.2","biotype":"protein_coding","ncbi_id":"221692","summary":"The protein encoded by this gene is a member of the phosphatase and actin regulator family of proteins. This family member can bind actin and regulate the reorganization of the actin cytoskeleton. It plays a role in tubule formation and in endothelial cell survival. Polymorphisms in this gene are associated with susceptibility to myocardial infarction, coronary artery disease and cervical artery dissection. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016]","start":12716805,"end":13295335,"strand":1,"description":"phosphatase and actin regulator 1 [Source:HGNC Symbol;Acc:HGNC:20990]"}, {"versioned_ensembl_gene_id":"ENSG00000282442.1","gene_symbol":"AC254944.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31890769,"end":31891501,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282891.1","gene_symbol":"STATH","gene_name":"statherin [Source:HGNC Symbol;Acc:HGNC:11369]","synonyms":"STR","biotype":"protein_coding","ncbi_id":"6779","summary":null,"start":69995930,"end":70002570,"strand":1,"description":"statherin [Source:HGNC Symbol;Acc:HGNC:11369]"}, {"versioned_ensembl_gene_id":"ENSG00000282554.1","gene_symbol":"AC254944.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31915115,"end":31923892,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282670.1","gene_symbol":"AC254944.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31923141,"end":31923932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282275.1","gene_symbol":"RN7SL628P","gene_name":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479451","summary":null,"start":31927931,"end":31928167,"strand":-1,"description":"RNA, 7SL, cytoplasmic 628, pseudogene [Source:HGNC Symbol;Acc:HGNC:46644]"}, {"versioned_ensembl_gene_id":"ENSG00000282207.1","gene_symbol":"AC254944.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":31930192,"end":31930690,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282689.1","gene_symbol":"ULK4P2","gene_name":"ULK4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15776]","synonyms":"FAM7A2,D-X","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"100288380","summary":null,"start":31937745,"end":31965690,"strand":-1,"description":"ULK4 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15776]"}, {"versioned_ensembl_gene_id":"ENSG00000282984.1","gene_symbol":"TBCE","gene_name":"tubulin folding cofactor E [Source:HGNC Symbol;Acc:HGNC:11582]","synonyms":"pac2,KCS1,KCS,HRD","biotype":"protein_coding","ncbi_id":"6905","summary":"Cofactor E is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]","start":235367360,"end":235452759,"strand":1,"description":"tubulin folding cofactor E [Source:HGNC Symbol;Acc:HGNC:11582]"}, {"versioned_ensembl_gene_id":"ENSG00000281757.4","gene_symbol":"AC254560.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42129815,"end":42131435,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280905.2","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CYP2D8P2,CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP,CPD6,P450C2D","biotype":"protein_coding","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126481,"end":42130888,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000282958.2","gene_symbol":"HNRNPR","gene_name":"heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]","synonyms":"HNRPR,hnRNP-R","biotype":"protein_coding","ncbi_id":"10236","summary":"This gene encodes an RNA-binding protein that is a member of the spliceosome C complex, which functions in pre-mRNA processing and transport. The encoded protein also promotes transcription at the c-fos gene. Alternative splicing results in multiple transcript variants. There are pseudogenes for this gene on chromosomes 4, 11, and 10. [provided by RefSeq, Jul 2014]","start":23311235,"end":23351800,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]"}, {"versioned_ensembl_gene_id":"ENSG00000282177.1","gene_symbol":"U8","gene_name":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":31957111,"end":31957243,"strand":-1,"description":"U8 small nucleolar RNA [Source:RFAM;Acc:RF00096]"}, {"versioned_ensembl_gene_id":"ENSG00000282701.1","gene_symbol":"DNM1P50","gene_name":"dynamin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48499]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"101927579","summary":null,"start":31967338,"end":31970605,"strand":1,"description":"dynamin 1 pseudogene 50 [Source:HGNC Symbol;Acc:HGNC:48499]"}, {"versioned_ensembl_gene_id":"ENSG00000283087.1","gene_symbol":"CPEB2","gene_name":"cytoplasmic polyadenylation element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21745]","synonyms":null,"biotype":"protein_coding","ncbi_id":"132864","summary":"The protein encoded by this gene is highly similar to cytoplasmic polyadenylation element binding protein (CPEB), an mRNA-binding protein that regulates cytoplasmic polyadenylation of mRNA as a trans factor in oogenesis and spermatogenesis. Studies of the similar gene in mice suggested a possible role of this protein in transcriptionally inactive haploid spermatids. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]","start":15006017,"end":15073496,"strand":1,"description":"cytoplasmic polyadenylation element binding protein 2 [Source:HGNC Symbol;Acc:HGNC:21745]"}, {"versioned_ensembl_gene_id":"ENSG00000282773.1","gene_symbol":"GOLGA8Q","gene_name":"golgin A8 family member Q [Source:HGNC Symbol;Acc:HGNC:44408]","synonyms":null,"biotype":"protein_coding","ncbi_id":"727909","summary":null,"start":31975928,"end":31986353,"strand":-1,"description":"golgin A8 family member Q [Source:HGNC Symbol;Acc:HGNC:44408]"}, {"versioned_ensembl_gene_id":"ENSG00000282967.1","gene_symbol":"HTN3","gene_name":"histatin 3 [Source:HGNC Symbol;Acc:HGNC:5284]","synonyms":"HIS2","biotype":"protein_coding","ncbi_id":"3347","summary":"This gene encodes a member of the histatin family of small, histidine-rich, cationic proteins. They function as antimicrobial peptides and are important components of the innate immune system. Histatins are found in saliva and exhibit antibacterial, antifungal activities and function in wound healing. [provided by RefSeq, Sep 2014]","start":70028413,"end":70036538,"strand":1,"description":"histatin 3 [Source:HGNC Symbol;Acc:HGNC:5284]"}, {"versioned_ensembl_gene_id":"ENSG00000282547.1","gene_symbol":"RN7SL796P","gene_name":"RNA, 7SL, cytoplasmic 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:46812]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"107080653","summary":null,"start":31977496,"end":31977786,"strand":-1,"description":"RNA, 7SL, cytoplasmic 796, pseudogene [Source:HGNC Symbol;Acc:HGNC:46812]"}, {"versioned_ensembl_gene_id":"ENSG00000281960.1","gene_symbol":"AC254960.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":31992464,"end":31998340,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282109.1","gene_symbol":"AC254960.2","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32024724,"end":32031065,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282068.1","gene_symbol":"AC254945.1","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":32117941,"end":32118087,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282629.1","gene_symbol":"RN7SL286P","gene_name":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479327","summary":null,"start":32132796,"end":32133086,"strand":1,"description":"RNA, 7SL, cytoplasmic 286, pseudogene [Source:HGNC Symbol;Acc:HGNC:46302]"}, {"versioned_ensembl_gene_id":"ENSG00000282824.1","gene_symbol":"MTND4P10","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42225]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873256","summary":null,"start":235543844,"end":235545206,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 10 [Source:HGNC Symbol;Acc:HGNC:42225]"}, {"versioned_ensembl_gene_id":"ENSG00000281931.1","gene_symbol":"SCG5","gene_name":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]","synonyms":"7B2,SgV,SGNE1,7B2,SgV,SGNE1","biotype":"protein_coding","ncbi_id":"6447","summary":"This gene encodes a secreted chaperone protein that prevents the aggregation of other secreted proteins, including proteins that are associated with neurodegenerative and metabolic disease. The encoded protein may be best known for its role in the trafficking and activation of prohormone convertase PC2 (encoded by Gene ID: 5126). Phosphorylation of the encoded protein has been shown to have an inhibitory effect on its chaperone function. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32172366,"end":32227841,"strand":1,"description":"secretogranin V [Source:HGNC Symbol;Acc:HGNC:10816]"}, {"versioned_ensembl_gene_id":"ENSG00000283046.1","gene_symbol":"HTN1","gene_name":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]","synonyms":"HIS1","biotype":"protein_coding","ncbi_id":"3346","summary":"This gene encodes a member of the histatin family of small, histidine-rich, cationic proteins. They function as antimicrobial peptides and are important components of the innate immune system. Histatins are found in saliva and exhibit antibacterial, antifungal activities and function in wound healing. [provided by RefSeq, Aug 2014]","start":70050402,"end":70058845,"strand":1,"description":"histatin 1 [Source:HGNC Symbol;Acc:HGNC:5283]"}, {"versioned_ensembl_gene_id":"ENSG00000283090.1","gene_symbol":"CSN1S2AP","gene_name":"casein alpha s2-like A, pseudogene [Source:HGNC Symbol;Acc:HGNC:20230]","synonyms":"CSN1S2A","biotype":"transcribed_unitary_pseudogene","ncbi_id":"286828","summary":"This locus is the equivalent of casein gamma in mouse (GeneID 12993) and is found in a cluster of casein genes, similar to other mammals. In human, the potential open reading frame that matches the homologous protein from other species is prematurely truncated shortly after the signal peptide. Therefore, this locus appears to be a pseudogene. [provided by RefSeq, Jul 2008]","start":70067389,"end":70085270,"strand":1,"description":"casein alpha s2-like A, pseudogene [Source:HGNC Symbol;Acc:HGNC:20230]"}, {"versioned_ensembl_gene_id":"ENSG00000284131.1","gene_symbol":"AC208162.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42136419,"end":42139915,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284297.1","gene_symbol":"AC208162.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42138046,"end":42139714,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281387.3","gene_symbol":"AC208162.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42146237,"end":42146692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281436.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42163591,"end":42168706,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000282868.1","gene_symbol":"PRR27","gene_name":"proline rich 27 [Source:HGNC Symbol;Acc:HGNC:33193]","synonyms":"C4orf40","biotype":"protein_coding","ncbi_id":"401137","summary":null,"start":70138066,"end":70181249,"strand":1,"description":"proline rich 27 [Source:HGNC Symbol;Acc:HGNC:33193]"}, {"versioned_ensembl_gene_id":"ENSG00000281897.2","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42173715,"end":42357301,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000282081.1","gene_symbol":"AC254945.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":32186776,"end":32203791,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282555.1","gene_symbol":"AC090877.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":32248010,"end":32249747,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283009.1","gene_symbol":"ZNF436","gene_name":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]","synonyms":"Zfp46,KIAA1710","biotype":"protein_coding","ncbi_id":"80818","summary":null,"start":23366912,"end":23376906,"strand":-1,"description":"zinc finger protein 436 [Source:HGNC Symbol;Acc:HGNC:20814]"}, {"versioned_ensembl_gene_id":"ENSG00000282862.1","gene_symbol":"RPS21P1","gene_name":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100271090","summary":null,"start":235436776,"end":235437022,"strand":1,"description":"ribosomal protein S21 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:36401]"}, {"versioned_ensembl_gene_id":"ENSG00000282046.1","gene_symbol":"GREM1","gene_name":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]","synonyms":"DAND2,CRAC1,CRAC1,CKTSF1B1,HMPS,CKTSF1B1,HMPS,gremlin,gremlin,DRM,DRM,DAND2","biotype":"protein_coding","ncbi_id":"26585","summary":"This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted glycosylated protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to relay the sonic hedgehog (SHH) signal from the polarizing region to the apical ectodermal ridge during limb bud outgrowth. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]","start":32248714,"end":32275847,"strand":1,"description":"gremlin 1, DAN family BMP antagonist [Source:HGNC Symbol;Acc:HGNC:2001]"}, {"versioned_ensembl_gene_id":"ENSG00000283106.1","gene_symbol":"ZNF436-AS1","gene_name":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]","synonyms":"FLJ90508,C1orf213","biotype":"antisense_RNA","ncbi_id":"148898","summary":null,"start":23376461,"end":23379303,"strand":1,"description":"ZNF436 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:25122]"}, {"versioned_ensembl_gene_id":"ENSG00000282880.1","gene_symbol":"B3GALNT2","gene_name":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]","synonyms":"MGC39558","biotype":"protein_coding","ncbi_id":"148789","summary":"This gene encodes a member of the glycosyltransferase 31 family. The encoded protein synthesizes GalNAc:beta-1,3GlcNAc, a novel carbohydrate structure, on N- and O-glycans. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2013]","start":235453714,"end":235508272,"strand":-1,"description":"beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]"}, {"versioned_ensembl_gene_id":"ENSG00000282829.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":23377718,"end":23377810,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283012.1","gene_symbol":"AL109936.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23385844,"end":23386493,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282941.1","gene_symbol":"TCEA3","gene_name":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]","synonyms":"TFIIS.H","biotype":"protein_coding","ncbi_id":"6920","summary":null,"start":23388525,"end":23432204,"strand":-1,"description":"transcription elongation factor A3 [Source:HGNC Symbol;Acc:HGNC:11615]"}, {"versioned_ensembl_gene_id":"ENSG00000282513.1","gene_symbol":"FMN1","gene_name":"formin 1 [Source:HGNC Symbol;Acc:HGNC:3768]","synonyms":"MGC125288,LD,FMN,FLJ45135,DKFZP686C2281,MGC125289","biotype":"protein_coding","ncbi_id":"342184","summary":"This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]","start":32296285,"end":32725473,"strand":-1,"description":"formin 1 [Source:HGNC Symbol;Acc:HGNC:3768]"}, {"versioned_ensembl_gene_id":"ENSG00000282918.1","gene_symbol":"MTCYBP14","gene_name":"mitochondrially encoded cytochrome b pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51960]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075120","summary":null,"start":235523762,"end":235524476,"strand":1,"description":"mitochondrially encoded cytochrome b pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:51960]"}, {"versioned_ensembl_gene_id":"ENSG00000283066.1","gene_symbol":"MTND6P14","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39477]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106478948","summary":null,"start":235541311,"end":235541832,"strand":1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 pseudogene 14 [Source:HGNC Symbol;Acc:HGNC:39477]"}, {"versioned_ensembl_gene_id":"ENSG00000283014.1","gene_symbol":"MTND5P19","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873270","summary":null,"start":235541843,"end":235543636,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 pseudogene 19 [Source:HGNC Symbol;Acc:HGNC:42301]"}, {"versioned_ensembl_gene_id":"ENSG00000282857.1","gene_symbol":"MTND4LP21","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075306","summary":null,"start":235545203,"end":235545497,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:42255]"}, {"versioned_ensembl_gene_id":"ENSG00000282903.1","gene_symbol":"AC098829.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":15008285,"end":15431257,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283116.1","gene_symbol":"MTND3P8","gene_name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100873185","summary":null,"start":235545550,"end":235545888,"strand":-1,"description":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 pseudogene 8 [Source:HGNC Symbol;Acc:HGNC:42153]"}, {"versioned_ensembl_gene_id":"ENSG00000282999.1","gene_symbol":"MTCO3P46","gene_name":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"107075293","summary":null,"start":235545950,"end":235546181,"strand":-1,"description":"mitochondrially encoded cytochrome c oxidase III pseudogene 46 [Source:HGNC Symbol;Acc:HGNC:52165]"}, {"versioned_ensembl_gene_id":"ENSG00000283105.1","gene_symbol":"AL357134.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":23418296,"end":23419610,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282972.1","gene_symbol":"GNG4","gene_name":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]","synonyms":null,"biotype":"protein_coding","ncbi_id":"2786","summary":null,"start":235551478,"end":235654545,"strand":-1,"description":"G protein subunit gamma 4 [Source:HGNC Symbol;Acc:HGNC:4407]"}, {"versioned_ensembl_gene_id":"ENSG00000283019.1","gene_symbol":"FO393422.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":235569552,"end":235570728,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283735.1","gene_symbol":"AL357556.3","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":235383547,"end":235384759,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282410.1","gene_symbol":"AC090877.3","gene_name":null,"synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":null,"summary":null,"start":32367723,"end":32368066,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282854.1","gene_symbol":"ASAP3","gene_name":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:14987]","synonyms":"UPLC1,FLJ20199,DDEFL1,CENTB6","biotype":"protein_coding","ncbi_id":"55616","summary":"This gene encodes a member of a subfamily of ADP-ribosylation factor(Arf) GTPase-activating proteins that contain additional ankyrin repeat and pleckstrin homology domains. The Arf GAP domain of this protein catalyzes the hydrolysis of GTP bound to Arf proteins. The encoded protein promotes cell differentiation and migration and has been implicated in cancer cell invasion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]","start":23436027,"end":23492032,"strand":-1,"description":"ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:HGNC:14987]"}, {"versioned_ensembl_gene_id":"ENSG00000283465.2","gene_symbol":"GOLGA8J","gene_name":"golgin A8 family member J [Source:HGNC Symbol;Acc:HGNC:38650]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653073","summary":null,"start":30083058,"end":30093489,"strand":1,"description":"golgin A8 family member J [Source:HGNC Symbol;Acc:HGNC:38650]"}, {"versioned_ensembl_gene_id":"ENSG00000284076.1","gene_symbol":"GOLGA8T","gene_name":"golgin A8 family member T [Source:HGNC Symbol;Acc:HGNC:44410]","synonyms":null,"biotype":"protein_coding","ncbi_id":"653075","summary":null,"start":30135046,"end":30148832,"strand":1,"description":"golgin A8 family member T [Source:HGNC Symbol;Acc:HGNC:44410]"}, {"versioned_ensembl_gene_id":"ENSG00000282088.2","gene_symbol":"AC254952.1","gene_name":"neuronal acetylcholine receptor subunit alpha-7 isoform 1 precursor [Source:RefSeq peptide;Acc:NP_000737]","synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":30371954,"end":30510022,"strand":-1,"description":"neuronal acetylcholine receptor subunit alpha-7 isoform 1 precursor [Source:RefSeq peptide;Acc:NP_000737]"}, {"versioned_ensembl_gene_id":"ENSG00000282276.1","gene_symbol":"ARHGAP11B","gene_name":"Rho GTPase activating protein 11B [Source:NCBI gene;Acc:89839]","synonyms":"B'-T,FAM7B1,B'-T,FAM7B1","biotype":"protein_coding","ncbi_id":"89839","summary":null,"start":31901490,"end":31914212,"strand":-1,"description":"Rho GTPase activating protein 11B [Source:NCBI gene;Acc:89839]"}, {"versioned_ensembl_gene_id":"ENSG00000283589.2","gene_symbol":"GOLGA8N","gene_name":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]","synonyms":null,"biotype":"protein_coding","ncbi_id":"643699","summary":null,"start":32124112,"end":32137984,"strand":1,"description":"golgin A8 family member N [Source:HGNC Symbol;Acc:HGNC:44405]"}, {"versioned_ensembl_gene_id":"ENSG00000282168.2","gene_symbol":"ARHGAP11A","gene_name":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]","synonyms":"KIAA0013,KIAA0013","biotype":"protein_coding","ncbi_id":"9824","summary":"This gene encodes a member of the Rho GTPase activating protein family. In response to DNA damage, the encoded protein interacts with the p53 tumor suppressor protein and stimulates its tetramerization, which results in cell-cycle arrest and apoptosis. A chromosomal deletion that includes this gene is one cause of Prader-Willi syndrome, and an intronic variant of this gene may be associated with sleep duration in children. This gene is highly expressed in colon cancers and in a human basal-like breast cancer cell line. This gene also produces a ARHGAP11A-SCG5 readthrough transcript and ARHGAP11A-SCG5 protein. [provided by RefSeq, Feb 2019]","start":32146897,"end":32166626,"strand":1,"description":"Rho GTPase activating protein 11A [Source:HGNC Symbol;Acc:HGNC:15783]"}, {"versioned_ensembl_gene_id":"ENSG00000282899.1","gene_symbol":"E2F2","gene_name":"E2F transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3114]","synonyms":"E2F-2","biotype":"protein_coding","ncbi_id":"1870","summary":"The protein encoded by this gene is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a dimerization domain which determines interaction with the differentiation regulated transcription factor proteins (DP), a transactivation domain enriched in acidic amino acids, and a tumor suppressor protein association domain which is embedded within the transactivation domain. This protein and another 2 members, E2F1 and E2F3, have an additional cyclin binding domain. This protein binds specifically to retinoblastoma protein pRB in a cell-cycle dependent manner, and it exhibits overall 46% amino acid identity to E2F1. [provided by RefSeq, Jul 2008]","start":23513894,"end":23538684,"strand":-1,"description":"E2F transcription factor 2 [Source:HGNC Symbol;Acc:HGNC:3114]"}, {"versioned_ensembl_gene_id":"ENSG00000282990.1","gene_symbol":"AL021154.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":23556603,"end":23558379,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283060.1","gene_symbol":"ID3","gene_name":"inhibitor of DNA binding 3, HLH protein [Source:HGNC Symbol;Acc:HGNC:5362]","synonyms":"HEIR-1,bHLHb25","biotype":"protein_coding","ncbi_id":"3399","summary":"The protein encoded by this gene is a helix-loop-helix (HLH) protein that can form heterodimers with other HLH proteins. However, the encoded protein lacks a basic DNA-binding domain and therefore inhibits the DNA binding of any HLH protein with which it interacts. [provided by RefSeq, Aug 2011]","start":23565382,"end":23567258,"strand":-1,"description":"inhibitor of DNA binding 3, HLH protein [Source:HGNC Symbol;Acc:HGNC:5362]"}, {"versioned_ensembl_gene_id":"ENSG00000283862.1","gene_symbol":"AC209232.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23257868,"end":23258239,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000279937.2","gene_symbol":"AL109936.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23342376,"end":23342561,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000280221.2","gene_symbol":"AL109936.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23392124,"end":23394364,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284267.1","gene_symbol":"AL021154.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":23511884,"end":23512255,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283185.1","gene_symbol":"PRAMEF28P","gene_name":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]","synonyms":"PRAMEF28","biotype":"unprocessed_pseudogene","ncbi_id":"102724742","summary":null,"start":13029339,"end":13032130,"strand":1,"description":"PRAME family member 28, pseudogene [Source:HGNC Symbol;Acc:HGNC:51890]"}, {"versioned_ensembl_gene_id":"ENSG00000283425.1","gene_symbol":"PRAMEF27","gene_name":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101929983","summary":null,"start":13049476,"end":13056491,"strand":-1,"description":"PRAME family member 27 [Source:HGNC Symbol;Acc:HGNC:51234]"}, {"versioned_ensembl_gene_id":"ENSG00000283292.1","gene_symbol":"HNRNPCL3","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]","synonyms":null,"biotype":"protein_coding","ncbi_id":"649330","summary":null,"start":13060869,"end":13062229,"strand":1,"description":"heterogeneous nuclear ribonucleoprotein C-like 3 [Source:HGNC Symbol;Acc:HGNC:51235]"}, {"versioned_ensembl_gene_id":"ENSG00000283244.1","gene_symbol":"AF250324.8","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":189780336,"end":189940271,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283348.2","gene_symbol":"PRAMEF25","gene_name":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]","synonyms":null,"biotype":"protein_coding","ncbi_id":"441873","summary":null,"start":13068677,"end":13077884,"strand":1,"description":"PRAME family member 25 [Source:HGNC Symbol;Acc:HGNC:49179]"}, {"versioned_ensembl_gene_id":"ENSG00000283032.1","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107763,"end":42108951,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000282848.1","gene_symbol":"MYO16","gene_name":"myosin XVI [Source:HGNC Symbol;Acc:HGNC:29822]","synonyms":"NYAP3,MYR8,Myo16b,KIAA0865,PPP1R107","biotype":"protein_coding","ncbi_id":"23026","summary":"This gene encodes an unconventional myosin protein. The encoded protein has been proposed to act as a serine/threonine phosphatase-1 targeting or regulatory subunit. Studies in a rat cell line suggest that this protein may regulate cell cycle progression. A variant within this gene may be associated with susceptibility to schizophrenia and elevated expression of this gene has been observed in the frontal cortex of human schizophrenia patients. [provided by RefSeq, Mar 2017]","start":108596152,"end":109212675,"strand":1,"description":"myosin XVI [Source:HGNC Symbol;Acc:HGNC:29822]"}, {"versioned_ensembl_gene_id":"ENSG00000283089.1","gene_symbol":"AC235563.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42124279,"end":42127773,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283661.1","gene_symbol":"PRAMEF34P","gene_name":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"649324","summary":null,"start":13095179,"end":13097971,"strand":-1,"description":"PRAME family member 34, pseudogene [Source:HGNC Symbol;Acc:HGNC:51895]"}, {"versioned_ensembl_gene_id":"ENSG00000283630.1","gene_symbol":"FRG1","gene_name":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]","synonyms":"FSG1,FRG1A","biotype":"protein_coding","ncbi_id":"2483","summary":"This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]","start":189940788,"end":189963204,"strand":1,"description":"FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]"}, {"versioned_ensembl_gene_id":"ENSG00000282969.1","gene_symbol":"AC235563.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42125906,"end":42127572,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283861.1","gene_symbol":"AC203630.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":24994838,"end":24995028,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283135.1","gene_symbol":"RN7SKP178","gene_name":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479175","summary":null,"start":205900630,"end":205900958,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 178 [Source:HGNC Symbol;Acc:HGNC:45902]"}, {"versioned_ensembl_gene_id":"ENSG00000283410.1","gene_symbol":"PRAMEF35P","gene_name":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100419649","summary":null,"start":13104403,"end":13105689,"strand":-1,"description":"PRAME family member 35, pseudogene [Source:HGNC Symbol;Acc:HGNC:51896]"}, {"versioned_ensembl_gene_id":"ENSG00000283134.1","gene_symbol":"AC007679.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":205949091,"end":205950145,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282884.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2DP1,CYP2D8P1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42147351,"end":42152466,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000282838.1","gene_symbol":"PRSS21","gene_name":"protease, serine 21 [Source:HGNC Symbol;Acc:HGNC:9485]","synonyms":"ESP-1,TEST1","biotype":"protein_coding","ncbi_id":"10942","summary":"This gene encodes a cell-surface anchored serine protease, which is a member of the trypsin family of serine proteases. The encoded protein is predicted to be active on peptide linkages involving the carboxyl group of lysine or arginine. The encoded protein localizes to the cytoplasm and the plasma membrane of premeiotic testicular germ cells and may be involved in progression of testicular tumors of germ cell origin. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]","start":2817180,"end":2826304,"strand":1,"description":"protease, serine 21 [Source:HGNC Symbol;Acc:HGNC:9485]"}, {"versioned_ensembl_gene_id":"ENSG00000282841.1","gene_symbol":"CTAGE1","gene_name":"cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:24346]","synonyms":"cTAGE-1,CTAGE,CT21.2,CT21.1,cTAGE-2","biotype":"protein_coding","ncbi_id":"64693","summary":null,"start":22413601,"end":22417915,"strand":-1,"description":"cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:HGNC:24346]"}, {"versioned_ensembl_gene_id":"ENSG00000283370.1","gene_symbol":"HNRNPCL2","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]","synonyms":"HNRNPCP5,HNRNPCP5","biotype":"protein_coding","ncbi_id":"440563","summary":null,"start":13115496,"end":13116854,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 2 [Source:HGNC Symbol;Acc:HGNC:48813]"}, {"versioned_ensembl_gene_id":"ENSG00000283315.1","gene_symbol":"AC007679.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":205989585,"end":206000858,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283107.1","gene_symbol":"AC099849.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":22418829,"end":22419294,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283079.1","gene_symbol":"LINC01515","gene_name":"long intergenic non-protein coding RNA 1515 [Source:HGNC Symbol;Acc:HGNC:51210]","synonyms":null,"biotype":"lincRNA","ncbi_id":"101928913","summary":null,"start":65574155,"end":65772652,"strand":1,"description":"long intergenic non-protein coding RNA 1515 [Source:HGNC Symbol;Acc:HGNC:51210]"}, {"versioned_ensembl_gene_id":"ENSG00000282839.1","gene_symbol":"RPS4XP18","gene_name":"ribosomal protein S4X pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36170]","synonyms":"RPS4P18","biotype":"processed_pseudogene","ncbi_id":"646583","summary":null,"start":22592145,"end":22592907,"strand":1,"description":"ribosomal protein S4X pseudogene 18 [Source:HGNC Symbol;Acc:HGNC:36170]"}, {"versioned_ensembl_gene_id":"ENSG00000284178.1","gene_symbol":"AC221035.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":22531612,"end":22532718,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283543.1","gene_symbol":"PRAMEF36P","gene_name":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"645354","summary":null,"start":13128818,"end":13131615,"strand":1,"description":"PRAME family member 36, pseudogene [Source:HGNC Symbol;Acc:HGNC:51897]"}, {"versioned_ensembl_gene_id":"ENSG00000283026.1","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42157475,"end":42341067,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000283624.1","gene_symbol":"AC245056.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":13146981,"end":13147460,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283510.1","gene_symbol":"INO80D","gene_name":"INO80 complex subunit D [Source:HGNC Symbol;Acc:HGNC:25997]","synonyms":"FLJ20309","biotype":"protein_coding","ncbi_id":"54891","summary":null,"start":205993721,"end":206086303,"strand":-1,"description":"INO80 complex subunit D [Source:HGNC Symbol;Acc:HGNC:25997]"}, {"versioned_ensembl_gene_id":"ENSG00000283216.1","gene_symbol":"PRAMEF26","gene_name":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645359","summary":null,"start":13148905,"end":13155961,"strand":-1,"description":"PRAME family member 26 [Source:HGNC Symbol;Acc:HGNC:49178]"}, {"versioned_ensembl_gene_id":"ENSG00000283231.1","gene_symbol":"HNRNPCL4","gene_name":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]","synonyms":null,"biotype":"protein_coding","ncbi_id":"101060301","summary":null,"start":13164586,"end":13165467,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein C-like 4 [Source:HGNC Symbol;Acc:HGNC:51333]"}, {"versioned_ensembl_gene_id":"ENSG00000283139.1","gene_symbol":"PRAMEF9","gene_name":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]","synonyms":null,"biotype":"protein_coding","ncbi_id":"343070","summary":null,"start":13172455,"end":13179464,"strand":1,"description":"PRAME family member 9 [Source:HGNC Symbol;Acc:HGNC:27996]"}, {"versioned_ensembl_gene_id":"ENSG00000283397.1","gene_symbol":"MLLT10P2","gene_name":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106480724","summary":null,"start":189973599,"end":189973847,"strand":-1,"description":"myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:39141]"}, {"versioned_ensembl_gene_id":"ENSG00000283437.1","gene_symbol":"AF146191.5","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":189979902,"end":189982379,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282837.2","gene_symbol":"AC254788.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42128127,"end":42141929,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283655.1","gene_symbol":"TUBB7P","gene_name":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]","synonyms":"TUBB4Q","biotype":"unprocessed_pseudogene","ncbi_id":"56604","summary":null,"start":189982523,"end":189984871,"strand":-1,"description":"tubulin beta 7 pseudogene [Source:HGNC Symbol;Acc:HGNC:12413]"}, {"versioned_ensembl_gene_id":"ENSG00000283804.1","gene_symbol":"AC254788.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42139408,"end":42141049,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282919.1","gene_symbol":"OLA1P1","gene_name":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"246785","summary":null,"start":42107765,"end":42108953,"strand":-1,"description":"Obg-like ATPase 1 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:45274]"}, {"versioned_ensembl_gene_id":"ENSG00000283308.1","gene_symbol":"RNA5SP174","gene_name":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]","synonyms":"RN5S174","biotype":"rRNA","ncbi_id":"106478998","summary":null,"start":190014800,"end":190014917,"strand":1,"description":"RNA, 5S ribosomal pseudogene 174 [Source:HGNC Symbol;Acc:HGNC:43074]"}, {"versioned_ensembl_gene_id":"ENSG00000283282.1","gene_symbol":"RNA5SP175","gene_name":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]","synonyms":"RN5S175","biotype":"rRNA","ncbi_id":"106480758","summary":null,"start":190017360,"end":190017478,"strand":1,"description":"RNA, 5S ribosomal pseudogene 175 [Source:HGNC Symbol;Acc:HGNC:43075]"}, {"versioned_ensembl_gene_id":"ENSG00000283184.1","gene_symbol":"DUX4L9","gene_name":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100288711","summary":null,"start":190021078,"end":190022336,"strand":-1,"description":"double homeobox 4 like 9 [Source:HGNC Symbol;Acc:HGNC:33855]"}, {"versioned_ensembl_gene_id":"ENSG00000283129.1","gene_symbol":"Vault","gene_name":"Vault RNA [Source:RFAM;Acc:RF00006]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206007880,"end":206007974,"strand":-1,"description":"Vault RNA [Source:RFAM;Acc:RF00006]"}, {"versioned_ensembl_gene_id":"ENSG00000283250.1","gene_symbol":"RARRES2P4","gene_name":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"644881","summary":null,"start":190037743,"end":190038226,"strand":-1,"description":"retinoic acid receptor responder 2 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:48703]"}, {"versioned_ensembl_gene_id":"ENSG00000283687.1","gene_symbol":"Y_RNA","gene_name":"Y RNA [Source:RFAM;Acc:RF00019]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206025593,"end":206025697,"strand":1,"description":"Y RNA [Source:RFAM;Acc:RF00019]"}, {"versioned_ensembl_gene_id":"ENSG00000283565.1","gene_symbol":"PRAMEF31P","gene_name":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"100129611","summary":null,"start":13216103,"end":13218892,"strand":1,"description":"PRAME family member 31, pseudogene [Source:HGNC Symbol;Acc:HGNC:51893]"}, {"versioned_ensembl_gene_id":"ENSG00000283641.1","gene_symbol":"AC007679.6","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206040432,"end":206040845,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283570.1","gene_symbol":"DUX4L8","gene_name":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]","synonyms":"DUX2","biotype":"unprocessed_pseudogene","ncbi_id":"26583","summary":"This gene is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that encodes two homeoboxes; the repeat-array and ORF is conserved in other mammals. There is no evidence for transcription of the gene at this locus though RT-PCR and in vitro expression experiments indicate that a telomeric paralog of this gene is transcribed in some haplotypes. Contraction of the macrosatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD). [provided by RefSeq, Jun 2014]","start":190067620,"end":190068894,"strand":1,"description":"double homeobox 4 like 8 [Source:HGNC Symbol;Acc:HGNC:38670]"}, {"versioned_ensembl_gene_id":"ENSG00000283192.1","gene_symbol":"AC007383.4","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":206084605,"end":206086564,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283150.1","gene_symbol":"PRAMEF5","gene_name":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]","synonyms":"PRAMEF5L,PRAMEF23","biotype":"protein_coding","ncbi_id":"343068","summary":null,"start":13224452,"end":13233554,"strand":1,"description":"PRAME family member 5 [Source:HGNC Symbol;Acc:HGNC:27995]"}, {"versioned_ensembl_gene_id":"ENSG00000284475.1","gene_symbol":"CT476828.19","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190070926,"end":190072197,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284002.1","gene_symbol":"CT476828.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190074232,"end":190075503,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283830.1","gene_symbol":"CT476828.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190077538,"end":190078809,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283898.1","gene_symbol":"CT476828.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190080844,"end":190082115,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284502.1","gene_symbol":"CT476828.21","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190084150,"end":190085421,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283650.1","gene_symbol":"PRAMEF32P","gene_name":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]","synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":"650236","summary":null,"start":13243779,"end":13245867,"strand":-1,"description":"PRAME family member 32, pseudogene [Source:HGNC Symbol;Acc:HGNC:51894]"}, {"versioned_ensembl_gene_id":"ENSG00000283017.1","gene_symbol":"ERC1","gene_name":"ELKS/RAB6-interacting/CAST family member 1 [Source:HGNC Symbol;Acc:HGNC:17072]","synonyms":"ELKS,CAST2,RAB6IP2,MGC12974,KIAA1081","biotype":"protein_coding","ncbi_id":"23085","summary":"The protein encoded by this gene is a member of a family of RIM-binding proteins. RIMs are active zone proteins that regulate neurotransmitter release. This gene has been found fused to the receptor-type tyrosine kinase gene RET by gene rearrangement due to the translocation t(10;12)(q11;p13) in thyroid papillary carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]","start":990509,"end":1502861,"strand":1,"description":"ELKS/RAB6-interacting/CAST family member 1 [Source:HGNC Symbol;Acc:HGNC:17072]"}, {"versioned_ensembl_gene_id":"ENSG00000202250.2","gene_symbol":"RNU6-771P","gene_name":"RNA, U6 small nuclear 771, pseudogene [Source:HGNC Symbol;Acc:HGNC:47734]","synonyms":"RNU6-1185P","biotype":"snRNA","ncbi_id":"106479907","summary":null,"start":13249365,"end":13249471,"strand":-1,"description":"RNA, U6 small nuclear 771, pseudogene [Source:HGNC Symbol;Acc:HGNC:47734]"}, {"versioned_ensembl_gene_id":"ENSG00000283387.1","gene_symbol":"PRAMEF8","gene_name":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]","synonyms":null,"biotype":"protein_coding","ncbi_id":"391002","summary":null,"start":13251275,"end":13255414,"strand":-1,"description":"PRAME family member 8 [Source:HGNC Symbol;Acc:HGNC:24074]"}, {"versioned_ensembl_gene_id":"ENSG00000282845.1","gene_symbol":"EIF1P4","gene_name":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100130566","summary":null,"start":2822659,"end":2822993,"strand":-1,"description":"eukaryotic translation initiation factor 1 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:49617]"}, {"versioned_ensembl_gene_id":"ENSG00000282966.1","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP,CPD6,P450C2D,CYP2D8P2","biotype":"protein_coding","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126481,"end":42130888,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000283056.1","gene_symbol":"ZG16B","gene_name":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]","synonyms":"PRO1567,JCLN2,HRPE773","biotype":"protein_coding","ncbi_id":"124220","summary":null,"start":2830169,"end":2839582,"strand":1,"description":"zymogen granule protein 16B [Source:HGNC Symbol;Acc:HGNC:30456]"}, {"versioned_ensembl_gene_id":"ENSG00000283022.1","gene_symbol":"HYDIN","gene_name":"HYDIN, axonemal central pair apparatus protein [Source:HGNC Symbol;Acc:HGNC:19368]","synonyms":"PPP1R31,KIAA1864,DKFZp434D0513,CILD5","biotype":"protein_coding","ncbi_id":"54768","summary":"This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]","start":70807378,"end":71230718,"strand":-1,"description":"HYDIN, axonemal central pair apparatus protein [Source:HGNC Symbol;Acc:HGNC:19368]"}, {"versioned_ensembl_gene_id":"ENSG00000283488.2","gene_symbol":"PRAMEF33","gene_name":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]","synonyms":"PRAMEF33P,PRAMEF33P","biotype":"protein_coding","ncbi_id":"645382","summary":null,"start":13273779,"end":13279147,"strand":1,"description":"PRAME family member 33 [Source:HGNC Symbol;Acc:HGNC:49193]"}, {"versioned_ensembl_gene_id":"ENSG00000284281.1","gene_symbol":"AC245056.5","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":13014766,"end":13015875,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284531.1","gene_symbol":"AC244216.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":13268552,"end":13268923,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283482.1","gene_symbol":"SNORA41","gene_name":"small nucleolar RNA, H/ACA box 41 [Source:HGNC Symbol;Acc:HGNC:32634]","synonyms":"SNORA41A,ACA41","biotype":"snoRNA","ncbi_id":"619569","summary":null,"start":206162228,"end":206162359,"strand":1,"description":"small nucleolar RNA, H/ACA box 41 [Source:HGNC Symbol;Acc:HGNC:32634]"}, {"versioned_ensembl_gene_id":"ENSG00000283070.3","gene_symbol":"PRSS30P","gene_name":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]","synonyms":"TMPRSS8P,TMPRSS8,MGC5228,Disp","biotype":"transcribed_unitary_pseudogene","ncbi_id":"124221","summary":null,"start":2839565,"end":2842741,"strand":-1,"description":"protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]"}, {"versioned_ensembl_gene_id":"ENSG00000283112.1","gene_symbol":"AC217628.1","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":2857891,"end":2859719,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283049.1","gene_symbol":"AC003965.3","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":2872278,"end":2873548,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282932.2","gene_symbol":"PTPRD","gene_name":"protein tyrosine phosphatase, receptor type D [Source:HGNC Symbol;Acc:HGNC:9668]","synonyms":"PTPD,HPTP","biotype":"protein_coding","ncbi_id":"5789","summary":"The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an extracellular region, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this protein is composed of three Ig-like and eight fibronectin type III-like domains. Studies of the similar genes in chicken and fly suggest the role of this PTP is in promoting neurite growth, and regulating neurons axon guidance. Multiple alternatively spliced transcript variants of this gene have been reported. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jan 2010]","start":8314246,"end":10617538,"strand":-1,"description":"protein tyrosine phosphatase, receptor type D [Source:HGNC Symbol;Acc:HGNC:9668]"}, {"versioned_ensembl_gene_id":"ENSG00000282937.3","gene_symbol":"PRSS22","gene_name":"protease, serine 22 [Source:HGNC Symbol;Acc:HGNC:14368]","synonyms":"BSSP-4,SP001LA,hBSSP-4,BSSP-4,SP001LA,hBSSP-4","biotype":"protein_coding","ncbi_id":"64063","summary":"This gene encodes a member of the trypsin family of serine proteases. The enzyme is expressed in the airways in a developmentally regulated manner. The gene is part of a cluster of serine protease genes on chromosome 16. [provided by RefSeq, Jul 2008]","start":2852693,"end":2858097,"strand":-1,"description":"protease, serine 22 [Source:HGNC Symbol;Acc:HGNC:14368]"}, {"versioned_ensembl_gene_id":"ENSG00000283447.1","gene_symbol":"NDUFS1","gene_name":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]","synonyms":"CI-75k","biotype":"protein_coding","ncbi_id":"4719","summary":"The protein encoded by this gene belongs to the complex I 75 kDa subunit family. Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. This protein is the largest subunit of complex I and it is a component of the iron-sulfur (IP) fragment of the enzyme. It may form part of the active site crevice where NADH is oxidized. Mutations in this gene are associated with complex I deficiency. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]","start":206114817,"end":206159603,"strand":-1,"description":"NADH:ubiquinone oxidoreductase core subunit S1 [Source:HGNC Symbol;Acc:HGNC:7707]"}, {"versioned_ensembl_gene_id":"ENSG00000283006.1","gene_symbol":"AC225828.1","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42132527,"end":42132982,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282979.1","gene_symbol":"AC254847.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42163834,"end":42167328,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282874.1","gene_symbol":"AC254847.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42165461,"end":42167127,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283008.1","gene_symbol":"CYP2D7","gene_name":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]","synonyms":"CYP2D7P,CYP2D,CYP2D@,CYP2D7P1","biotype":"polymorphic_pseudogene","ncbi_id":"1564","summary":"This gene is a member of the cytochrome P450 gene superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This gene is a segregating pseudogene, where some individuals may have an allele that encodes a functional enzyme, while other individuals have an allele encoding a protein that is predicted to be non-functional. In this case, the functional allele is thought to be rare. This locus is part of a cluster of cytochrome P450 genes on chromosome 22. [provided by RefSeq, Jan 2017]","start":42167604,"end":42171978,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) [Source:HGNC Symbol;Acc:HGNC:2624]"}, {"versioned_ensembl_gene_id":"ENSG00000282926.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2D8P1,CYP2DP1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42177288,"end":42182405,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000282892.1","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42187414,"end":42371000,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000283015.1","gene_symbol":"AC009136.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":71306328,"end":71307614,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000282830.1","gene_symbol":"CALB2","gene_name":"calbindin 2 [Source:HGNC Symbol;Acc:HGNC:1435]","synonyms":"CAL2","biotype":"protein_coding","ncbi_id":"794","summary":"This gene encodes an intracellular calcium-binding protein belonging to the troponin C superfamily. Members of this protein family have six EF-hand domains which bind calcium. This protein plays a role in diverse cellular functions, including message targeting and intracellular calcium buffering. It also functions as a modulator of neuronal excitability, and is a diagnostic marker for some human diseases, including Hirschsprung disease and some cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]","start":71363481,"end":71395226,"strand":1,"description":"calbindin 2 [Source:HGNC Symbol;Acc:HGNC:1435]"}, {"versioned_ensembl_gene_id":"ENSG00000282945.2","gene_symbol":"CMTR2","gene_name":"cap methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:25635]","synonyms":"FTSJD1,FLJ11171,AFT,MTr2,FTSJD1,FLJ11171,AFT,MTr2","biotype":"protein_coding","ncbi_id":"55783","summary":null,"start":71283583,"end":71285892,"strand":-1,"description":"cap methyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:25635]"}, {"versioned_ensembl_gene_id":"ENSG00000284106.1","gene_symbol":"AC009136.2","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":71293954,"end":71294528,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283260.1","gene_symbol":"AC007383.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":206115547,"end":206122323,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283168.1","gene_symbol":"GCSHP3","gene_name":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100329109","summary":null,"start":206116110,"end":206116500,"strand":-1,"description":"glycine cleavage system protein H pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:43929]"}, {"versioned_ensembl_gene_id":"ENSG00000283391.1","gene_symbol":"EEF1B2","gene_name":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]","synonyms":null,"biotype":"protein_coding","ncbi_id":"1933","summary":"This gene encodes a translation elongation factor. The protein is a guanine nucleotide exchange factor involved in the transfer of aminoacylated tRNAs to the ribosome. Alternative splicing results in three transcript variants which differ only in the 5' UTR. [provided by RefSeq, Jul 2008]","start":206159585,"end":206162928,"strand":1,"description":"eukaryotic translation elongation factor 1 beta 2 [Source:HGNC Symbol;Acc:HGNC:3208]"}, {"versioned_ensembl_gene_id":"ENSG00000283254.1","gene_symbol":"uc_338","gene_name":"TUC338 [Source:RFAM;Acc:RF02271]","synonyms":null,"biotype":"misc_RNA","ncbi_id":null,"summary":null,"start":206160843,"end":206161024,"strand":1,"description":"TUC338 [Source:RFAM;Acc:RF02271]"}, {"versioned_ensembl_gene_id":"ENSG00000283323.1","gene_symbol":"snoZ196","gene_name":"Small nucleolar RNA Z196/R39/R59 family [Source:RFAM;Acc:RF00134]","synonyms":null,"biotype":"snoRNA","ncbi_id":null,"summary":null,"start":206161841,"end":206161929,"strand":1,"description":"Small nucleolar RNA Z196/R39/R59 family [Source:RFAM;Acc:RF00134]"}, {"versioned_ensembl_gene_id":"ENSG00000283671.1","gene_symbol":"SNORD51","gene_name":"small nucleolar RNA, C/D box 51 [Source:HGNC Symbol;Acc:HGNC:10201]","synonyms":"U51,RNU51","biotype":"snoRNA","ncbi_id":"26798","summary":null,"start":206161878,"end":206161957,"strand":1,"description":"small nucleolar RNA, C/D box 51 [Source:HGNC Symbol;Acc:HGNC:10201]"}, {"versioned_ensembl_gene_id":"ENSG00000282942.1","gene_symbol":"RPS26P3","gene_name":"ribosomal protein S26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23411]","synonyms":"bA338L20.1","biotype":"processed_pseudogene","ncbi_id":"441386","summary":null,"start":9095713,"end":9096060,"strand":1,"description":"ribosomal protein S26 pseudogene 3 [Source:HGNC Symbol;Acc:HGNC:23411]"}, {"versioned_ensembl_gene_id":"ENSG00000283643.1","gene_symbol":"GPR1-AS","gene_name":"GPR1 antisense RNA [Source:NCBI gene;Acc:101669764]","synonyms":"GPR1AS,GPR1-AS1","biotype":"processed_transcript","ncbi_id":"101669764","summary":"This gene is thought to produce a non-coding RNA. It is situated adjacent to a differentially methylated region (DMR) and is imprinted and paternally expressed in the placenta. [provided by RefSeq, Nov 2015]","start":206203376,"end":206270863,"strand":1,"description":"GPR1 antisense RNA [Source:NCBI gene;Acc:101669764]"}, {"versioned_ensembl_gene_id":"ENSG00000283395.1","gene_symbol":"RN7SKP200","gene_name":"RNA, 7SK small nuclear pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:45924]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106480895","summary":null,"start":206221316,"end":206221635,"strand":1,"description":"RNA, 7SK small nuclear pseudogene 200 [Source:HGNC Symbol;Acc:HGNC:45924]"}, {"versioned_ensembl_gene_id":"ENSG00000283357.1","gene_symbol":"HMGN1P6","gene_name":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"100874430","summary":null,"start":206264248,"end":206264538,"strand":-1,"description":"high mobility group nucleosome binding domain 1 pseudogene 6 [Source:HGNC Symbol;Acc:HGNC:39349]"}, {"versioned_ensembl_gene_id":"ENSG00000281402.2","gene_symbol":"RN7SKP260","gene_name":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]","synonyms":null,"biotype":"misc_RNA","ncbi_id":"106479211","summary":null,"start":206264686,"end":206264834,"strand":-1,"description":"RNA, 7SK small nuclear pseudogene 260 [Source:HGNC Symbol;Acc:HGNC:45984]"}, {"versioned_ensembl_gene_id":"ENSG00000283649.1","gene_symbol":"ZDBF2","gene_name":"zinc finger DBF-type containing 2 [Source:HGNC Symbol;Acc:HGNC:29313]","synonyms":"Slx9,KIAA1571,FLJ45338","biotype":"protein_coding","ncbi_id":"57683","summary":"This gene encodes a protein containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]","start":206279283,"end":206319048,"strand":1,"description":"zinc finger DBF-type containing 2 [Source:HGNC Symbol;Acc:HGNC:29313]"}, {"versioned_ensembl_gene_id":"ENSG00000283169.1","gene_symbol":"AC017081.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":206414707,"end":206415529,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283305.1","gene_symbol":"HNRNPA1P51","gene_name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"729366","summary":null,"start":206423912,"end":206424858,"strand":-1,"description":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 [Source:HGNC Symbol;Acc:HGNC:48781]"}, {"versioned_ensembl_gene_id":"ENSG00000283995.1","gene_symbol":"AC007383.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":206171153,"end":206171530,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284455.1","gene_symbol":"AC017081.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":206360359,"end":206360736,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284091.1","gene_symbol":"AC017081.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":206360659,"end":206405805,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284220.1","gene_symbol":"AC017081.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":206404825,"end":206405196,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283825.1","gene_symbol":"LINC01982","gene_name":"long intergenic non-protein coding RNA 1982 [Source:HGNC Symbol;Acc:HGNC:52812]","synonyms":null,"biotype":"lincRNA","ncbi_id":"105371830","summary":null,"start":52390515,"end":52535701,"strand":1,"description":"long intergenic non-protein coding RNA 1982 [Source:HGNC Symbol;Acc:HGNC:52812]"}, {"versioned_ensembl_gene_id":"ENSG00000283747.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"CD85l,LILRA6P,ILT9","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283916.1","gene_symbol":"AC245128.23","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284211.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284539.1","gene_symbol":"VAV3-AS1","gene_name":"VAV3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40608]","synonyms":null,"biotype":"antisense_RNA","ncbi_id":"100873946","summary":null,"start":107964443,"end":107994607,"strand":1,"description":"VAV3 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:40608]"}, {"versioned_ensembl_gene_id":"ENSG00000284051.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284338.1","gene_symbol":"AL390036.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":108040263,"end":108076020,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283715.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283872.1","gene_symbol":"AC245128.21","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283942.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"LILRA5,CD85m,ILT10,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000283875.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736533,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000283917.1","gene_symbol":"AC079298.5","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154142124,"end":154305912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283681.1","gene_symbol":"TCF20","gene_name":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]","synonyms":"SPBP,AR1","biotype":"protein_coding","ncbi_id":"6942","summary":"This gene encodes a transcription factor that recognizes the platelet-derived growth factor-responsive element in the matrix metalloproteinase 3 promoter. The encoded protein is thought to be a transcriptional coactivator, enhancing the activity of transcription factors such as JUN and SP1. Mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]","start":42173689,"end":42357278,"strand":-1,"description":"transcription factor 20 [Source:HGNC Symbol;Acc:HGNC:11631]"}, {"versioned_ensembl_gene_id":"ENSG00000283140.2","gene_symbol":"AC255093.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42141601,"end":42143577,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283373.2","gene_symbol":"AC255093.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":42155260,"end":42157236,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284581.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284104.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736542,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284468.1","gene_symbol":"SLC25A24","gene_name":"solute carrier family 25 member 24 [Source:HGNC Symbol;Acc:HGNC:20662]","synonyms":"DKFZp586G0123,APC1","biotype":"protein_coding","ncbi_id":"29957","summary":"This gene encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]","start":108134003,"end":108200843,"strand":-1,"description":"solute carrier family 25 member 24 [Source:HGNC Symbol;Acc:HGNC:20662]"}, {"versioned_ensembl_gene_id":"ENSG00000284420.1","gene_symbol":"AC270107.11","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":21544470,"end":21545630,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284072.1","gene_symbol":"AC270107.6","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":21700313,"end":21700603,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283730.1","gene_symbol":"AC091946.3","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":21746820,"end":21910080,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283963.1","gene_symbol":"AC270107.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21522076,"end":21527875,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283851.1","gene_symbol":"AC270107.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21533079,"end":21535169,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284137.1","gene_symbol":"LLGL1","gene_name":"LLGL1, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6628]","synonyms":"Mgl1,LLGL,Lgl1,HUGL-1,HUGL,DLG4","biotype":"protein_coding","ncbi_id":"3996","summary":"This gene encodes a protein that is similar to a tumor suppressor in Drosophila. The protein is part of a cytoskeletal network and is associated with nonmuscle myosin II heavy chain and a kinase that specifically phosphorylates this protein at serine residues. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":18225587,"end":18244875,"strand":1,"description":"LLGL1, scribble cell polarity complex component [Source:HGNC Symbol;Acc:HGNC:6628]"}, {"versioned_ensembl_gene_id":"ENSG00000284036.1","gene_symbol":"AC270107.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21542357,"end":21548155,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283989.1","gene_symbol":"AC270107.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21561834,"end":21567636,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283720.1","gene_symbol":"AC270107.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21572841,"end":21574931,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283284.1","gene_symbol":"CYP2D6","gene_name":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]","synonyms":"CYP2D7AP,P450-DB1,CYP2D7P2,CYP2D,CYP2DL1,CYP2D7BP,CPD6,P450C2D,CYP2D8P2","biotype":"protein_coding","ncbi_id":"1565","summary":"This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is known to metabolize as many as 25% of commonly prescribed drugs. Its substrates include antidepressants, antipsychotics, analgesics and antitussives, beta adrenergic blocking agents, antiarrythmics and antiemetics. The gene is highly polymorphic in the human population; certain alleles result in the poor metabolizer phenotype, characterized by a decreased ability to metabolize the enzyme's substrates. Some individuals with the poor metabolizer phenotype have no functional protein since they carry 2 null alleles whereas in other individuals the gene is absent. This gene can vary in copy number and individuals with the ultrarapid metabolizer phenotype can have 3 or more active copies of the gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","start":42126498,"end":42130905,"strand":-1,"description":"cytochrome P450 family 2 subfamily D member 6 [Source:HGNC Symbol;Acc:HGNC:2625]"}, {"versioned_ensembl_gene_id":"ENSG00000284287.1","gene_symbol":"AC270107.10","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21582121,"end":21587921,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284434.1","gene_symbol":"AC270107.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21592308,"end":21594398,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284227.1","gene_symbol":"DCHS2","gene_name":"dachsous cadherin-related 2 [Source:HGNC Symbol;Acc:HGNC:23111]","synonyms":"CDHR7,CDHJ,CDH27,PCDHJ,PCDH23,FLJ20047","biotype":"protein_coding","ncbi_id":"54798","summary":"This gene encodes a large protein that contains many cadherin domains and likely functions in cell adhesion. Genome-wide association studies suggest that this gene may be important in Alzheimer's disease, compressive strength index, and appendicular lean mass. [provided by RefSeq, May 2017]","start":154239130,"end":154498809,"strand":-1,"description":"dachsous cadherin-related 2 [Source:HGNC Symbol;Acc:HGNC:23111]"}, {"versioned_ensembl_gene_id":"ENSG00000284230.1","gene_symbol":"AC270107.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21601596,"end":21607404,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284168.1","gene_symbol":"AC270107.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21612607,"end":21614697,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283910.1","gene_symbol":"AC245128.22","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798302,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284151.1","gene_symbol":"AC270107.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":21621899,"end":21627692,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284132.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"p58,CD158B2,cl-6,nkat2,nkat2a,nkat2b","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738512,"end":54753069,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284497.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755039,"end":54767385,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000283962.1","gene_symbol":"KP420439.2","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798294,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284169.1","gene_symbol":"KU645196.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54786328,"end":54797950,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284504.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738520,"end":54753046,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284514.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769828,"end":54784338,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284319.1","gene_symbol":"AC275454.2","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":108199920,"end":108201485,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283911.1","gene_symbol":"AC275454.1","gene_name":null,"synonyms":null,"biotype":"TEC","ncbi_id":null,"summary":null,"start":108200407,"end":108202737,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284432.1","gene_symbol":"AC275455.3","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":108494877,"end":108500545,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283723.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769820,"end":54784331,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284110.1","gene_symbol":"ST13P21","gene_name":"ST13, Hsp70 interacting protein pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38864]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"642818","summary":null,"start":108501780,"end":108502877,"strand":1,"description":"ST13, Hsp70 interacting protein pseudogene 21 [Source:HGNC Symbol;Acc:HGNC:38864]"}, {"versioned_ensembl_gene_id":"ENSG00000284199.1","gene_symbol":"AL392088.3","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":108507994,"end":108508663,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283707.1","gene_symbol":"AC275455.1","gene_name":null,"synonyms":null,"biotype":"pseudogene","ncbi_id":null,"summary":null,"start":108472947,"end":108473674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284396.1","gene_symbol":"AC275455.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":108487916,"end":108488296,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283893.1","gene_symbol":"CT476828.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190087456,"end":190088727,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284156.1","gene_symbol":"CT476828.13","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190090762,"end":190092033,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284507.1","gene_symbol":"CT476828.22","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190094068,"end":190095339,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284066.1","gene_symbol":"CT476828.12","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190097374,"end":190098645,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284174.1","gene_symbol":"CT476828.14","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190100680,"end":190101951,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283834.1","gene_symbol":"CT476828.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190103986,"end":190105257,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284298.1","gene_symbol":"HM190170.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":190107292,"end":190108563,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284467.1","gene_symbol":"AC079298.6","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154243073,"end":154244691,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283841.1","gene_symbol":"AC079298.4","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":154268828,"end":154269286,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283957.1","gene_symbol":"AC110775.2","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":154380979,"end":154381440,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284571.1","gene_symbol":"FLII","gene_name":"FLII, actin remodeling protein [Source:HGNC Symbol;Acc:HGNC:3750]","synonyms":"MGC39265,FLIL,Fli1,FLI","biotype":"protein_coding","ncbi_id":"2314","summary":"This gene encodes a protein with a gelsolin-like actin binding domain and an N-terminal leucine-rich repeat-protein protein interaction domain. The protein is similar to a Drosophila protein involved in early embryogenesis and the structural organization of indirect flight muscle. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]","start":18244836,"end":18258916,"strand":-1,"description":"FLII, actin remodeling protein [Source:HGNC Symbol;Acc:HGNC:3750]"}, {"versioned_ensembl_gene_id":"ENSG00000284021.1","gene_symbol":"LGALS9C","gene_name":"galectin 9C [Source:HGNC Symbol;Acc:HGNC:33874]","synonyms":null,"biotype":"protein_coding","ncbi_id":"654346","summary":"This gene was initially thought to represent a pseudogene of galectin 9; however, this transcript has good exon-intron structure and encodes a predicted protein of the same size as and highly similar to galectin 9. This gene is one of two similar loci on chromosome 17p similar to galectin 9 and now thought to be protein-encoding. This gene is the more telomeric gene. [provided by RefSeq, Jul 2008]","start":18486342,"end":18504550,"strand":1,"description":"galectin 9C [Source:HGNC Symbol;Acc:HGNC:33874]"}, {"versioned_ensembl_gene_id":"ENSG00000284312.1","gene_symbol":"NOS2P2","gene_name":"nitric oxide synthase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7874]","synonyms":"NOS2B","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"201288","summary":null,"start":18506700,"end":18515918,"strand":-1,"description":"nitric oxide synthase 2 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:7874]"}, {"versioned_ensembl_gene_id":"ENSG00000283981.1","gene_symbol":"AC127537.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18297782,"end":18298690,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284320.1","gene_symbol":"AC127537.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18347515,"end":18355998,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284001.1","gene_symbol":"AC127537.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":18348247,"end":18348672,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283919.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786371,"end":54790334,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284105.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786364,"end":54790327,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284365.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803554,"end":54814536,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000283173.1","gene_symbol":"AC255093.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":42132544,"end":42132999,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283961.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"CD158D,15.212,103AS","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803543,"end":54814528,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000281053.2","gene_symbol":"AC255093.1","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42136436,"end":42139932,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000281266.2","gene_symbol":"AC255093.2","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":42138063,"end":42139731,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283628.1","gene_symbol":"CYP2D8P","gene_name":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]","synonyms":"CYP2D8P1,CYP2DP1","biotype":"unprocessed_pseudogene","ncbi_id":"1568","summary":null,"start":42163563,"end":42168680,"strand":-1,"description":"ccytochrome P450 family 2 subfamily D member 8, pseudogene [Source:HGNC Symbol;Acc:HGNC:2628]"}, {"versioned_ensembl_gene_id":"ENSG00000284426.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816487,"end":54830797,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000283954.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816479,"end":54830810,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000283727.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832695,"end":54848588,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000284307.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"cl-39,CD158i,nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832708,"end":54848388,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000284295.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850462,"end":54867223,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000284384.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850262,"end":54867032,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283722.1","gene_symbol":"KP420439.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54755017,"end":54767350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284495.1","gene_symbol":"MIEF2","gene_name":"mitochondrial elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:17920]","synonyms":"SMCR7,MiD49,MGC23130","biotype":"protein_coding","ncbi_id":"125170","summary":"This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]","start":18260534,"end":18266552,"strand":1,"description":"mitochondrial elongation factor 2 [Source:HGNC Symbol;Acc:HGNC:17920]"}, {"versioned_ensembl_gene_id":"ENSG00000284449.1","gene_symbol":"AC127537.9","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18268080,"end":18268828,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284238.1","gene_symbol":"TOP3A","gene_name":"topoisomerase (DNA) III alpha [Source:HGNC Symbol;Acc:HGNC:11992]","synonyms":"ZGRF7,TOP3","biotype":"protein_coding","ncbi_id":"7156","summary":"This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This enzyme catalyzes the transient breaking and rejoining of a single strand of DNA which allows the strands to pass through one another, thus reducing the number of supercoils and altering the topology of DNA. This enzyme forms a complex with BLM which functions in the regulation of recombination in somatic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]","start":18271428,"end":18315007,"strand":-1,"description":"topoisomerase (DNA) III alpha [Source:HGNC Symbol;Acc:HGNC:11992]"}, {"versioned_ensembl_gene_id":"ENSG00000284212.1","gene_symbol":"AC127537.7","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18311904,"end":18312651,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283753.1","gene_symbol":"AC127537.4","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18312760,"end":18313533,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283741.1","gene_symbol":"SMCR8","gene_name":"Smith-Magenis syndrome chromosome region, candidate 8 [Source:HGNC Symbol;Acc:HGNC:17921]","synonyms":"FLJ34716","biotype":"protein_coding","ncbi_id":"140775","summary":null,"start":18315310,"end":18328055,"strand":1,"description":"Smith-Magenis syndrome chromosome region, candidate 8 [Source:HGNC Symbol;Acc:HGNC:17921]"}, {"versioned_ensembl_gene_id":"ENSG00000284492.1","gene_symbol":"MIR6778","gene_name":"microRNA 6778 [Source:HGNC Symbol;Acc:HGNC:50183]","synonyms":"hsa-mir-6778","biotype":"miRNA","ncbi_id":"102466733","summary":"microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]","start":18340814,"end":18340886,"strand":-1,"description":"microRNA 6778 [Source:HGNC Symbol;Acc:HGNC:50183]"}, {"versioned_ensembl_gene_id":"ENSG00000284166.1","gene_symbol":"EVPLL","gene_name":"envoplakin like [Source:HGNC Symbol;Acc:HGNC:35236]","synonyms":null,"biotype":"protein_coding","ncbi_id":"645027","summary":null,"start":18387267,"end":18399252,"strand":1,"description":"envoplakin like [Source:HGNC Symbol;Acc:HGNC:35236]"}, {"versioned_ensembl_gene_id":"ENSG00000284566.1","gene_symbol":"AL353997.12","gene_name":null,"synonyms":null,"biotype":"antisense_RNA","ncbi_id":null,"summary":null,"start":18389460,"end":18398589,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284422.1","gene_symbol":"AL353997.10","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18398476,"end":18399064,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284444.1","gene_symbol":"AL353997.11","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18399758,"end":18399928,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284576.1","gene_symbol":"TBC1D3P4","gene_name":"TBC1 domain family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32409]","synonyms":"USP6P2","biotype":"unprocessed_pseudogene","ncbi_id":"100631253","summary":null,"start":18403085,"end":18410566,"strand":1,"description":"TBC1 domain family member 3 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:32409]"}, {"versioned_ensembl_gene_id":"ENSG00000284456.1","gene_symbol":"LINC02076","gene_name":"long intergenic non-protein coding RNA 2076 [Source:HGNC Symbol;Acc:HGNC:52924]","synonyms":"FLJ35934","biotype":"lincRNA","ncbi_id":"400579","summary":null,"start":18420764,"end":18423985,"strand":1,"description":"long intergenic non-protein coding RNA 2076 [Source:HGNC Symbol;Acc:HGNC:52924]"}, {"versioned_ensembl_gene_id":"ENSG00000284350.1","gene_symbol":"KRT17P5","gene_name":"keratin 17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50723]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339240","summary":null,"start":18425333,"end":18434702,"strand":1,"description":"keratin 17 pseudogene 5 [Source:HGNC Symbol;Acc:HGNC:50723]"}, {"versioned_ensembl_gene_id":"ENSG00000283850.1","gene_symbol":"YWHAEP2","gene_name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49429]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"106481688","summary":null,"start":18427800,"end":18427911,"strand":-1,"description":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:49429]"}, {"versioned_ensembl_gene_id":"ENSG00000283947.1","gene_symbol":"AL353997.7","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":18433926,"end":18434702,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284257.1","gene_symbol":"KRT17P2","gene_name":"keratin 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6429]","synonyms":null,"biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"339241","summary":null,"start":18436466,"end":18441453,"strand":1,"description":"keratin 17 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:6429]"}, {"versioned_ensembl_gene_id":"ENSG00000284527.1","gene_symbol":"KRT16P1","gene_name":"keratin 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6420]","synonyms":"KRT14P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"729252","summary":null,"start":18441656,"end":18452500,"strand":1,"description":"keratin 16 pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:6420]"}, {"versioned_ensembl_gene_id":"ENSG00000284285.1","gene_symbol":"KRT16P4","gene_name":"keratin 16 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37809]","synonyms":null,"biotype":"transcribed_processed_pseudogene","ncbi_id":"339244","summary":null,"start":18459849,"end":18485525,"strand":1,"description":"keratin 16 pseudogene 4 [Source:HGNC Symbol;Acc:HGNC:37809]"}, {"versioned_ensembl_gene_id":"ENSG00000284205.1","gene_symbol":"AL353997.9","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":18462560,"end":18462667,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284014.1","gene_symbol":"AL353997.8","gene_name":null,"synonyms":null,"biotype":"processed_pseudogene","ncbi_id":null,"summary":null,"start":18463179,"end":18463344,"strand":-1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283924.1","gene_symbol":"TNPO1P2","gene_name":"transportin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45121]","synonyms":null,"biotype":"processed_pseudogene","ncbi_id":"252968","summary":null,"start":18469996,"end":18472660,"strand":1,"description":"transportin 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:45121]"}, {"versioned_ensembl_gene_id":"ENSG00000284389.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284348.1","gene_symbol":"AC245128.32","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284296.1","gene_symbol":"AC245128.29","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284097.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284593.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284136.1","gene_symbol":"AC245128.26","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798077,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284249.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754806,"end":54767156,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284326.1","gene_symbol":"AC245128.31","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284141.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,CD85m,ILT10,LILRA5","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284371.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736535,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284100.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769600,"end":54784118,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000283823.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724488,"end":54736506,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284409.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284183.1","gene_symbol":"AC245128.28","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284590.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284030.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284472.1","gene_symbol":"AC245128.36","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283806.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284304.1","gene_symbol":"AC245128.30","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798270,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283837.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284405.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284164.1","gene_symbol":"AC245128.27","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284355.1","gene_symbol":"AC245128.33","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284510.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738512,"end":54753036,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000283800.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"ILT10,CD85m,ILT10,LILRA5,CD85m","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284374.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284462.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283748.1","gene_symbol":"AC245128.18","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284314.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000283915.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724485,"end":54736500,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284086.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724485,"end":54736499,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284545.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54867917,"end":54868023,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000283966.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736502,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284401.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769797,"end":54784308,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284480.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"CD158z,KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724485,"end":54736499,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284322.1","gene_symbol":"KU645195.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724505,"end":54798268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283996.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738485,"end":54753037,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284088.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755008,"end":54767354,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284245.1","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54873222,"end":54889446,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000283902.1","gene_symbol":"KU645196.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54803509,"end":54814091,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284119.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIRX,KIR48,KIR3DS2P,KIR2DS6,CD158C","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786151,"end":54790110,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284530.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"nkat1,cl-42,CD158A,47.11,p58.1","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769797,"end":54784306,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000283778.1","gene_symbol":"KP420438.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724502,"end":54798229,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283708.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738477,"end":54752995,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000283702.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738478,"end":54753016,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284248.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754966,"end":54767314,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284022.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54788439,"end":54788545,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000284555.1","gene_symbol":"KP420444.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54754709,"end":54768703,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283790.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738479,"end":54753006,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000283832.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR15,KIR2DL6,KIRY,KIRZ","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754987,"end":54767335,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000283729.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816294,"end":54830607,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000284451.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54789705,"end":54789811,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000284533.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR2DL6,KIRY,KIRZ,KIR15","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754977,"end":54767325,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000283901.1","gene_symbol":"KP420442.1","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724502,"end":54798256,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284236.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738479,"end":54753024,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284232.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIR2DL6,KIRY,KIRZ,KIR15","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754995,"end":54767341,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000283713.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786341,"end":54790304,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284145.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"CD158A,47.11,p58.1,nkat1,cl-42","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769754,"end":54784266,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000283953.1","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54795009,"end":54811233,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000284551.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"47.11,p58.1,nkat1,cl-42,CD158A","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769784,"end":54784293,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284466.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"CD158K,nkat4a,nkat4b,cl-5,nkat4","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54877873,"end":54894659,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283974.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786338,"end":54790301,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284509.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803507,"end":54814530,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000284102.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR48,KIR3DS2P,KIR2DS6,CD158C,KIRX","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786299,"end":54790262,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000283968.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54892652,"end":54896615,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284006.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786326,"end":54790289,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284101.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54983223,"end":55000011,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283869.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803469,"end":54814492,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000284524.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54896391,"end":54896497,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000284589.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816470,"end":54830783,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000284213.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54849415,"end":54866185,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283750.1","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54901697,"end":54917921,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000284392.1","gene_symbol":"KP420443.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54769815,"end":54783640,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284046.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850469,"end":54867221,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000284177.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"cl-11,AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816481,"end":54830792,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000283739.1","gene_symbol":"AC245128.17","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54918122,"end":54918869,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284113.1","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54933599,"end":54943589,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000283731.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"AMB11,cl-2,CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816443,"end":54830754,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000283811.1","gene_symbol":"KU645197.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54755007,"end":54767327,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284537.1","gene_symbol":"KP420437.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54738524,"end":54752340,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284408.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832690,"end":54848582,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000284063.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850452,"end":54867238,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000284562.1","gene_symbol":"KU645197.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54803528,"end":54814110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284206.1","gene_symbol":"KP420442.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54803494,"end":54814110,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284301.1","gene_symbol":"KU645196.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54816484,"end":54830365,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283779.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"nkat8,KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832652,"end":54848544,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000283986.1","gene_symbol":"KP420437.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54803317,"end":54813933,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283970.1","gene_symbol":"KU645196.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54833122,"end":54858674,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284016.1","gene_symbol":"KU645196.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54864894,"end":54867012,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283975.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4b,cl-5,nkat4,CD158K,nkat4a","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850414,"end":54867200,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283784.1","gene_symbol":"KU645196.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54908920,"end":54919502,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284111.1","gene_symbol":"KU645197.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54816504,"end":54830385,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283870.1","gene_symbol":"KP420437.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54832594,"end":54846912,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284264.1","gene_symbol":"KP420442.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54832770,"end":54847967,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284235.1","gene_symbol":"KU645197.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54833142,"end":54858873,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283937.1","gene_symbol":"KU645197.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54861549,"end":54875374,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283889.1","gene_symbol":"KU645196.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54921895,"end":54935776,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284414.1","gene_symbol":"KU645196.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54938533,"end":54964264,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284120.1","gene_symbol":"KU645196.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54966899,"end":54980724,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284302.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"LILRA6P,ILT9,CD85l","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283833.1","gene_symbol":"AC245128.20","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283983.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284037.1","gene_symbol":"KP420444.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54738527,"end":54752346,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284528.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54815973,"end":54832763,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283746.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000284563.1","gene_symbol":"AC245128.37","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283794.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284470.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283860.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRY,KIRZ,KIR15,KIR2DL6","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54785376,"end":54797726,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284133.1","gene_symbol":"AC245128.25","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284417.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR3DS2P,KIR2DS6,CD158C,KIRX,KIR48","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54816720,"end":54820679,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000283964.1","gene_symbol":"LILRP1","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]","synonyms":"ILT9,CD85l,LILRA6P","biotype":"unprocessed_pseudogene","ncbi_id":"79167","summary":null,"start":54696604,"end":54700905,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:15496]"}, {"versioned_ensembl_gene_id":"ENSG00000283732.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000283810.1","gene_symbol":"AC245128.19","gene_name":null,"synonyms":null,"biotype":"unprocessed_pseudogene","ncbi_id":null,"summary":null,"start":54703952,"end":54704235,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284339.1","gene_symbol":"LILRP2","gene_name":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]","synonyms":"CD85m,ILT10,LILRA5,CD85m,ILT10","biotype":"transcribed_processed_pseudogene","ncbi_id":"79166","summary":null,"start":54707916,"end":54713453,"strand":1,"description":"leukocyte immunoglobulin-like receptor pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:15497]"}, {"versioned_ensembl_gene_id":"ENSG00000284044.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738496,"end":54753018,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284478.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRY,KIRZ,KIR15,KIR2DL6","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54754989,"end":54767345,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284127.1","gene_symbol":"KIR3DL3","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]","synonyms":"KIRC1,KIR44,KIR3DL7,CD158z,KIRC1,KIR44,KIR3DL7,CD158z","biotype":"protein_coding","ncbi_id":"115653","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]","start":54724479,"end":54736532,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:16312]"}, {"versioned_ensembl_gene_id":"ENSG00000284423.1","gene_symbol":"AC245128.34","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798268,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284333.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738513,"end":54753035,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284381.1","gene_symbol":"KP420444.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771248,"end":54784342,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284053.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54908019,"end":54924805,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283725.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRZ,KIR15,KIR2DL6,KIRY","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755006,"end":54767354,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284004.1","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54793746,"end":54809970,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000284347.1","gene_symbol":"KIR2DL1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]","synonyms":"p58.1,nkat1,cl-42,CD158A,47.11","biotype":"protein_coding","ncbi_id":"3802","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54769794,"end":54784305,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6329]"}, {"versioned_ensembl_gene_id":"ENSG00000284013.1","gene_symbol":"KP420444.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54789901,"end":54800474,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284441.1","gene_symbol":"AC245128.35","gene_name":null,"synonyms":null,"biotype":"processed_transcript","ncbi_id":null,"summary":null,"start":54724496,"end":54798231,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284241.1","gene_symbol":"KIR2DL3","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]","synonyms":"CD158B2,cl-6,nkat2,nkat2a,nkat2b,p58","biotype":"protein_coding","ncbi_id":"3804","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54738511,"end":54753057,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3 [Source:HGNC Symbol;Acc:HGNC:6331]"}, {"versioned_ensembl_gene_id":"ENSG00000284303.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54834495,"end":54834601,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000284313.1","gene_symbol":"KIR2DP1","gene_name":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]","synonyms":"KIRZ,KIR15,KIR2DL6,KIRY","biotype":"unprocessed_pseudogene","ncbi_id":"554300","summary":null,"start":54755028,"end":54767374,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16344]"}, {"versioned_ensembl_gene_id":"ENSG00000284007.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786301,"end":54790264,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284061.1","gene_symbol":"FCAR","gene_name":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]","synonyms":"CD89","biotype":"protein_coding","ncbi_id":"2204","summary":"This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]","start":54839804,"end":54856028,"strand":1,"description":"Fc fragment of IgA receptor [Source:HGNC Symbol;Acc:HGNC:3608]"}, {"versioned_ensembl_gene_id":"ENSG00000284093.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"CD158E1,KIR,nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816446,"end":54830759,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000284397.1","gene_symbol":"KIR3DP1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]","synonyms":"KIR2DS6,CD158C,KIRX,KIR48,KIR3DS2P","biotype":"transcribed_unprocessed_pseudogene","ncbi_id":"548594","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]","start":54786338,"end":54790301,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains pseudogene 1 [Source:HGNC Symbol;Acc:HGNC:16343]"}, {"versioned_ensembl_gene_id":"ENSG00000284511.1","gene_symbol":"KP420440.8","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54724500,"end":54738318,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284460.1","gene_symbol":"KIR2DL4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]","synonyms":"15.212,103AS,CD158D","biotype":"protein_coding","ncbi_id":"3805","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]","start":54803507,"end":54814530,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6332]"}, {"versioned_ensembl_gene_id":"ENSG00000283763.1","gene_symbol":"KU645198.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54773309,"end":54775435,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283716.1","gene_symbol":"KP420440.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54740683,"end":54754627,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284089.1","gene_symbol":"KP420440.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54757172,"end":54766181,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284039.1","gene_symbol":"KP420440.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54768588,"end":54782742,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284580.1","gene_symbol":"KP420440.9","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54800209,"end":54814175,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283925.1","gene_symbol":"AC245128.24","gene_name":null,"synonyms":null,"biotype":"lincRNA","ncbi_id":null,"summary":null,"start":54856229,"end":54856976,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284457.1","gene_symbol":"KP420440.7","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54833895,"end":54844477,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284192.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850445,"end":54867195,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000284208.1","gene_symbol":"NCR1","gene_name":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]","synonyms":"NKP46,NK-p46,LY94,CD335,NKP46,NK-p46,LY94,CD335","biotype":"protein_coding","ncbi_id":"9437","summary":null,"start":54871706,"end":54881696,"strand":1,"description":"natural cytotoxicity triggering receptor 1 [Source:HGNC Symbol;Acc:HGNC:6731]"}, {"versioned_ensembl_gene_id":"ENSG00000284342.1","gene_symbol":"KP420444.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54802867,"end":54816638,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284033.1","gene_symbol":"KP420441.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54738532,"end":54752350,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284279.1","gene_symbol":"RNU6-222P","gene_name":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]","synonyms":null,"biotype":"snRNA","ncbi_id":"106479665","summary":null,"start":54868927,"end":54869033,"strand":-1,"description":"RNA, U6 small nuclear 222, pseudogene [Source:HGNC Symbol;Acc:HGNC:47185]"}, {"versioned_ensembl_gene_id":"ENSG00000284244.1","gene_symbol":"KP420444.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54819131,"end":54834306,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283827.1","gene_symbol":"KIR3DL1","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]","synonyms":"nkat3,CD158e1/2,NKB1,CD158e2,NKB1B,cl-11,cl-2,KIR,nkat3,NKB1,NKB1B,AMB11,CD158E1,CD158e1/2,CD158e2,cl-11,AMB11,cl-2,CD158E1,KIR","biotype":"protein_coding","ncbi_id":"3811","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54816481,"end":54830792,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1 [Source:HGNC Symbol;Acc:HGNC:6338]"}, {"versioned_ensembl_gene_id":"ENSG00000284318.1","gene_symbol":"KP420444.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54840112,"end":54842280,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284225.1","gene_symbol":"KP420441.4","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54754713,"end":54768701,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284340.1","gene_symbol":"KP420446.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54803469,"end":54814085,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283742.1","gene_symbol":"KP420441.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54771254,"end":54780267,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284217.1","gene_symbol":"KP420441.3","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54782674,"end":54797006,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284560.1","gene_symbol":"KP420441.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54799641,"end":54813466,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283719.1","gene_symbol":"KP420440.2","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54846871,"end":54860752,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284354.1","gene_symbol":"KP420440.6","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54863509,"end":54872498,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000284150.1","gene_symbol":"KP420440.5","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54891695,"end":54905520,"strand":1,"description":null}, {"versioned_ensembl_gene_id":"ENSG00000283846.1","gene_symbol":"KIR2DS4","gene_name":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]","synonyms":"KKA3,cl-39,nkat8,KKA3,CD158i,nkat8,cl-39,CD158i,KKA3,cl-39,CD158i,nkat8","biotype":"polymorphic_pseudogene","ncbi_id":"3809","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]","start":54832690,"end":54848582,"strand":1,"description":"killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 [Source:HGNC Symbol;Acc:HGNC:6336]"}, {"versioned_ensembl_gene_id":"ENSG00000283951.1","gene_symbol":"KIR3DL2","gene_name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]","synonyms":"nkat4,CD158K,nkat4a,nkat4b,cl-5","biotype":"protein_coding","ncbi_id":"3812","summary":"Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several \"framework\" genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the \"framework\" loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]","start":54850452,"end":54867240,"strand":1,"description":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2 [Source:HGNC Symbol;Acc:HGNC:6339]"}, {"versioned_ensembl_gene_id":"ENSG00000283882.1","gene_symbol":"KP420446.1","gene_name":null,"synonyms":null,"biotype":"protein_coding","ncbi_id":null,"summary":null,"start":54832746,"end":54847943,"strand":1,"description":null}]